650-RICR-20-05-5
650-RICR-20-05-5. RICRMP: Ocean SAMP - Chapter 5 - Commercial and Recreational Fisheries (version Amendment, 08/12/2013 to 08/17/2018)
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Chapter 5: Commercial and Recreational Fisheries
Table of Contents
500 Introduction........................................................................................................................9
510 Marine Fisheries Resources in the Ocean SAMP Area...................................................12
510.1 Species Included in this Chapter.......................................................................12
510.1.1 Species important to commercial and recreational fisheries....................12
510.1.2 Forage fish ............................................................................................15
510.1.3 Threatened and endangered species and species of concern ...................15
510.2 Life History, Habitat, and Fishery of Commercially and Recreationally
Important Species .......................................................................................................17
510.2.1 American lobster ...................................................................................17
510.2.2 Atlantic bonito.......................................................................................19
510.2.3 Atlantic cod...........................................................................................20
510.2.4 Atlantic herring .....................................................................................21
510.2.5 Atlantic mackerel ..................................................................................23
510.2.6 Atlantic sea scallop................................................................................25
510.2.7 Black sea bass .......................................................................................26
510.2.8 Bluefish.................................................................................................28
510.2.9 Butterfish...............................................................................................30
510.2.10 False albacore......................................................................................31
510.2.11 Goosefish (monkfish) ......................................................................... 32
510.2.12 Longfin squid ......................................................................................33
510.2.13 Menhaden............................................................................................35
510.2.14 Scup ....................................................................................................36
510.2.15 Shark, Blue..........................................................................................37
510.2.16 Shark, Shortfin mako...........................................................................38
510.2.17 Shark, Thresher ...................................................................................39
510.2.18 Silver hake...........................................................................................40
510.2.19 Skates..................................................................................................42
510.2.20 Spiny dogfish ......................................................................................43
510.2.21 Striped bass .........................................................................................44
510.2.22 Summer flounder.................................................................................46
510.2.23 Tautog.................................................................................................48
510.2.24 Tuna, Bluefin.......................................................................................49
510.2.25 Tuna, Yellowfin...................................................................................51
510.2.26 Winter flounder ...................................................................................52
510.2.27 Yellowtail flounder..............................................................................53
510.3 Stocks of Concern ..............................................................................................55
510.3.1 Georges Bank and Southward Cod.........................................................55
510.3.2 Southern New England/Mid-Atlantic winter flounder ............................56
510.3.3 Southern New England/Mid-Atlantic yellowtail flounder.......................56
510.3.4 Butterfish...............................................................................................57
510.4 Forage Fish.........................................................................................................57
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510.5 Threatened and Endangered Species and Species of Concern.........................58
510.5.1 Atlantic halibut......................................................................................58
510.5.2 Atlantic sturgeon ...................................................................................59
510.5.3 Atlantic wolffish....................................................................................60
510.5.4 Dusky shark...........................................................................................60
510.5.5 Porbeagle shark .....................................................................................61
510.5.6 Rainbow smelt.......................................................................................62
510.5.7 River herring (alewife and blueback herring)........................................ 62
510.5.8 Sand tiger shark.....................................................................................63
510.5.9 Thorny skate..........................................................................................63
510.6 Baseline Characterization of Species of Importance ........................................64
510.6.1 Analysis of Total Catch Biomass ...........................................................68
510.6.2 Analysis of Catch by Individual Species ................................................72
520 Fish Habitat in the Ocean SAMP Area ...........................................................................76
520.1 Benthic Habitat ..................................................................................................76
520.2 Habitat Requirements for Species of Importance.............................................76
520.3 Essential Fish Habitat........................................................................................78
520.4 Critical Habitat ..................................................................................................85
530 Commercial and Recreational Fisheries in the Ocean SAMP Area ...............................86
530.1 History of Fisheries in Rhode Island.................................................................86
530.1.1 Commercial Fishing History..................................................................86
530.1.2 Recreational Fishing History .................................................................90
530.2 Rhode Island Commercial and Recreational Fishing Ports .............................90
530.2.1 Point Judith/Galilee ...............................................................................91
530.2.2 Newport ................................................................................................94
530.2.3 Sakonnet Point ......................................................................................96
530.2.4 Block Island ..........................................................................................96
530.2.5 Other Commercial and Recreational Fishing Ports.................................97
530.3 Description of Rhode Island’s Fisheries............................................................98
530.3.1 Bottom Types, Seasonal Migrations, and Fishing...................................98
530.3.2 Mapping Fishing Activity Areas............................................................98
530.4 Contemporary Commercial Mobile Gear Fisheries .......................................102
530.4.1 Description..........................................................................................102
530.4.2 Mobile Gear Fishing Activity Areas ....................................................103
530.5 Contemporary Commercial Fixed Gear Fisheries .........................................109
530.5.1 Description...........................................................................................109
530.5.2 Fixed Gear Fishing Activity Areas........................................................111
530.6 Rhode Island Commercial Fisheries Effort and Landings.............................114
530.6.1 RI Commercial Fisheries Landings......................................................114
530.6.2 RI Commercial Fishing Effort .............................................................118
530.7 Contemporary Recreational and For-Hire Fishing........................................124
530.7.1 Description..........................................................................................124
530.7.2 Recreational Fishing Catch and Effort Data.........................................125
530.7.3 Recreational and For-Hire Fishing Activity Areas................................131
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540 Economic Impact of Commercial and Recreational Fisheries......................................133
540.1 Commercial Fisheries Landings Value and Economic Impact ......................133
540.1.1 Point Judith .........................................................................................135
540.1.2 Newport ..............................................................................................137
540.2 Economic Impact of Recreational Fishing ......................................................142
550 Impacts of Existing Activities and Trends on Fisheries Resources and Habitats........146
550.1 Fisheries and Overfishing................................................................................146
550.2 Coastal Development .......................................................................................148
550.3 Introduced Species...........................................................................................148
550.4 Marine Transportation....................................................................................149
550.5 Dredged Material Disposal..............................................................................149
550.6 Marine Debris ..................................................................................................150
550.7 Marine Fisheries Diseases................................................................................150
550.8 Global Climate Change....................................................................................150
560 Policies and Standards ...................................................................................................151
560.1 General Policies................................................................................................151
560.2 Regulatory Standards ......................................................................................152
570 Works Cited....................................................................................................................157
Appendices
A. Baseline Characterization: Data Sources, Methods, and Results .............separate cover
B. Fisheries Activity Maps: Methods and Data Sources................................separate cover
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Tables
Table 5.1. Commercially and recreationally important species. .................................................13
Table 5.2. Management and status of species/stocks in the Ocean SAMP area...........................14
Table 5.3. Habitat characteristics of American lobster...............................................................18
Table 5.4. Habitat characteristics of Atlantic bonito...................................................................19
Table 5.5. Habitat characteristics of Atlantic cod.......................................................................21
Table 5.6. Habitat characteristics of Atlantic herring. ................................................................22
Table 5.7. Habitat characteristics of Atlantic mackerel. .............................................................24
Table 5.8. Habitat characteristics of Atlantic sea scallop............................................................26
Table 5.9. Habitat characteristics of black sea bass....................................................................27
Table 5.10. Habitat characteristics of bluefish ...........................................................................29
Table 5.11. Habitat characteristics of butterfish.........................................................................30
Table 5.12. Habitat characteristics of false albacore. .................................................................32
Table 5.13. Habitat characteristics of goosefish (monkfish).......................................................33
Table 5.14. Habitat characteristics of longfin (loligo) squid.......................................................34
Table 5.15. Habitat characteristics of menhaden........................................................................36
Table 5.16. Habitat characteristics of scup.................................................................................37
Table 5.17. Habitat characteristics of blue shark........................................................................38
Table 5.18. Habitat characteristics of mako shark......................................................................39
Table 5.19. Habitat characteristics of thresher shark..................................................................40
Table 5.20. Habitat characteristics of silver hake.......................................................................41
Table 5.21. Habitat characteristics of little skate........................................................................43
Table 5.22. Habitat characteristics of winter skate.....................................................................43
Table 5.23. Habitat characteristics of spiny dogfish...................................................................44
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Table 5.24. Habitat characteristics of striped bass......................................................................46
Table 5.25. Habitat characteristics of summer flounder .............................................................47
Table 5.26. Habitat characteristics of tautog. . ...........................................................................49
Table 5.27. Habitat characteristics of bluefin tuna. ....................................................................50
Table 5.28. Habitat characteristics of yellowfin tuna. ...............................................................51
Table 5.29. Habitat characteristics of winter flounder. ..............................................................53
Table 5.30. Habitat characteristics of yellowtail flounder. .........................................................54
Table 5.31. Species assessed in the baseline characterization.....................................................68
Table 5.32. Habitat requirements for species of importance found within the Ocean SAMP area.
.................................................................................................................................................77
Table 5.33. Species for which Essential Fish Habitat has been designated within the Ocean
SAMP area................................................................................................................................78
Table 5.34. Top landed species in Rhode Island by weight for 1999-2008...............................115
Table 5.35. Average number of trips on which species were landed (state data), 2007-2009....119
Table 5.36. Rhode Island landings by gear type, 1999-2008. ..................................................121
Table 5.37. Average number of trips per month by gear type, 2007-2009 . .............................123
Table 5.38. Party and charter boat licenses issued by year. .....................................................125
Table 5.39. Estimated average recreational catch, 1999-2008..................................................128
Table 5.40. Top landed species in Rhode Island by value averaged for 1999-2008. ...............134
Table 5.41. Federal vessel permits and landings value between 1997 and 2006 for Point Judith/
Narragansett............................................................................................................................136
Table 5.42. Dollar value of landings of federally managed groups of species for Point Judith 136
Table 5.43. Federal vessel permits and landings value between 1997 and 2006 for Newport....137
Table 5.44. Dollar value for landings of federally managed species for Newport.....................138
Table 5.45. Economic impacts of commercial fishing industry in Rhode Island in 2006 ..........141
Table 5.46. Total number of Rhode Island seafood commerce establishments and employees .141
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Table 5.47. Fisheries sector employment impacts, 2005. .........................................................142
Table 5.48. Angler trip expenses, 2006....................................................................................144
Table 5.49. Durable equipment expenditures, 2006. ................................................................144
Table 5.50. Economic impacts from recreational fishing in Rhode Island, 1999-2005. ............144
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Figures
Figure 5.1. Locations of survey stations used in baseline characterization .................................66
Figure 5.2. Results of multi-way ANOVA of total biomass .......................................................69
Figure 5.3. Aggregate fish biomass, spring, 1999-2008 ............................................................70
Figure 5.4. Aggregate fish biomass, fall, 1999-2008.................................................................71
Figure 5.5. Total biomass per area by species, 1999-2008 .........................................................72
Figure 5.6. DEM trawl survey biomass per area by species, 1999-2008.....................................73
Figure 5.7. GSO trawl survey biomass per area by species, 1999-2008......................................73
Figure 5.8. NMFS trawl survey biomass per area by species, 1999-2008...................................74
Figure 5.9. NEAMAP trawl survey biomass per area by species, 2007-2008.............................74
Figure 5.10. Spring and fall biomass of species identified as a driver of demersal fish and
invertebrate community composition.........................................................................................75
Figure 5.11. Number of species per ten minute square with designated Essential Fish Habitat,......
all life stages .............................................................................................................................80
Figure 5.12. Number of species per ten minute square with designated Essential Fish Habitat,......
egg life stage.............................................................................................................................81
Figure 5.13. Number of species per ten minute square with designated Essential Fish Habitat,......
larval life stage..........................................................................................................................82
Figure 5.14. Number of species per ten minute square with designated Essential Fish Habitat,......
juvenile life stage ......................................................................................................................83
Figure 5.15. Number of species per ten minute square with designated Essential Fish Habitat,......
adult life stage...........................................................................................................................84
Figure 5.16. Historic trawling areas...........................................................................................88
Figure 5.17. Mobile gear, fixed gear, and recreational fishing areas based on qualitative input 100
Figure 5.18. Mobile gear and gillnet fishing areas based on NMFS Vessel Trip Reports..........101
Figure 5.19. Mobile gear fishing areas based on qualitative input ............................................105
Figure 5.20. Bottom trawling areas based on NMFS Vessel Trip Reports................................106
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Figure 5.21. Scallop dredging areas based on NMFS Vessel Trip Reports...............................107
Figure 5.22. Mid-water trawling areas based on NMFS Vessel Trip Reports ...........................108
Figure 5.23. Currently active or permitted floating fish trap areas............................................110
Figure 5.24. Fixed gear fishing areas based on qualitative input ..............................................112
Figure 5.25. Gillnet fishing areas based on NMFS Vessel Trip Reports...................................113
Figure 5.26. Top landed species in RI by weight for 1999-2008 ..............................................116
Figure 5.27. Top landed species in RI by dollar value averaged for 1999-2008........................117
Figure 5.28. RI landings by weight, 1970-2008.......................................................................118
Figure 5.29. NMFS statistical areas.........................................................................................120
Figure 5.30. RI landings in pounds by gear type for 1999-2008...............................................122
Figure 5.31. Estimated average recreational catch by species, 1999-2008................................127
Figure 5.32. Estimated recreational fishing trips and participants, 1999-2008..........................129
Figure 5.33. Estimated recreational fishing participants by residency, 1999-2008....................130
Figure 5.34. Estimated recreational fishing trips by mode, 1999-2008.....................................130
Figure 5.35. Recreational and charter boat fishing areas based on qualitative input..................132
Figure 5.36. RI commercial landings by value, 1999-2008 ......................................................135
Figure 5.37. Point Judith landings by dollar value and weight, 1999-2008...............................137
Figure 5.38. Newport landings by dollar value and weight, 1999-2008....................................138
Figure 5.39. Ranking by pounds of commercial fishery landings at major U.S. ports...............139
Figure 5.40. Ranking by dollar value of commercial fishery landings at major U.S. ports........140
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Section 500. Introduction
1. Commercial and recreational fisheries are among the oldest and most widespread human
uses of the Ocean SAMP area and are of great economic, historic and cultural value to
the state of Rhode Island. Commercial fisheries sustain Rhode Island coastal
communities by providing jobs to fishermen and supporting businesses and industries, as
well as food for local consumption or export throughout the United States and overseas.
Recreational fisheries, which here includes recreational fishing that takes place aboard
for-hire party and charter boats as well as recreational anglers fishing from private boats,
also support businesses and families throughout Rhode Island and are a key element of
the region’s recreation and tourism economy. All Rhode Island fisheries, both within the
Ocean SAMP area and inside Narragansett Bay, also have significant non-market value
in that they provide Rhode Islanders with a connection to the sea and to New England’s
rich maritime history.
2. The purpose of the Ocean SAMP is to protect sustainable existing uses, resources, and
habitats, and to guide future uses of the Ocean SAMP area. While it is recognized there is
a need to restore fish habitat and recover depleted stocks, the goal of the Ocean SAMP is
not to engage in fisheries management. Commercial and recreational fisheries in the
Ocean SAMP area are already managed by a host of different agencies and regulatory
bodies which have jurisdiction over different species and/or different parts of the Ocean
SAMP area. In many cases, these entities have overlapping jurisdiction over the state and
federal waters of the Ocean SAMP area. Entities involved in managing fish and fisheries
within the Ocean SAMP area include, but are not limited to, the Atlantic States Marine
Fisheries Commission (ASMFC), the Rhode Island Department of Environmental
Management (RIDEM), the New England Fishery Management Council, the Mid-
Atlantic Fishery Management Council, and the NOAA National Marine Fisheries Service
(NMFS).1 For further information on fisheries management, see Chapter 10, Existing
Statutes, Regulations, and Policies.
3. The objectives of this chapter are to summarize existing information about current
commercial and recreational fisheries resources and activities within the Ocean SAMP
area; highlight the economic, social, cultural, and historic value of these activities to
Rhode Island; and outline policies for managing these activities within the context of
other existing and future uses. Accordingly, this chapter focuses primarily on
commercially and recreationally important species that are targeted within the Ocean
SAMP area by Rhode Island fishermen. The methodology for selecting these species is
outlined below in Section 510. This chapter focuses on current baseline conditions based
on the best available existing data and information. Per the NMFS Northeast Regional
Office Protected Resources Division, this chapter also includes discussion of finfish
“Species of Concern” which may occur within the Ocean SAMP area; see Section 510
below for a list of those species included here. Available fisheries dependent and
independent data from the past decade are used to establish baseline conditions.
Available historic information on fisheries is included to underscore the longstanding
economic and cultural importance of these activities to Rhode Island.
1 In addition, the Rhode Island Marine Fisheries Council acts as an advisory group to the RIDEM Director.
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4. This chapter has found that commercial and recreational fisheries are an important
activity in the Ocean SAMP area. Twenty-eight finfish, shellfish, and crustacean species
are of commercial and recreational fishing importance in the Ocean SAMP area.
Commercial fishermen using otter trawls, scallop dredges, gillnets, and lobster pots
harvest a diverse variety of species, and squid and lobster are consistently among the
most valuable species landed in Rhode Island. Recreational fishermen fish in the Ocean
SAMP area aboard both private boats and party and charter boats, and target a variety of
species including striped bass, bluefish, summer flounder, and large pelagic fish. At the
time of this writing, many of the more popular commercially and recreationally targeted
species, including squid, summer flounder, scup, and striped bass, are not overfished, nor
is overfishing occurring. However, other fisheries are depleted or in decline, and there is
a need to rebuild the stocks of some species found in the Ocean SAMP area. There are a
variety of state and federal entities and regulatory bodies currently addressing stock
levels, largely through the development and implementation of Fishery Management
Plans. Fisheries management efforts have had a number of successes in rebuilding
previously overfished stocks. Whereas all of these species rely on habitat within the
Ocean SAMP area, little fish habitat mapping has been done to date at a resolution that
would highlight important habitats within the area. Available qualitative and quantitative
data have been used to produce maps that show commercial and recreational fisheries
activity throughout the Ocean SAMP area. These maps show that the entire Ocean SAMP
area is used by commercial and recreational fishermen over the course of a year, but that
these use patterns vary in space and time due to factors including seasonal species
migrations, the regulatory environment, and market demand for seafood. Commercial and
recreational fisheries have a longstanding history in Rhode Island and are closely tied to
Rhode Island’s coastal communities and economies; whereas commercial fisheries have
an economic impact through the sale and processing of seafood products, recreational
fisheries have an economic impact through the sale of fishing vessels and gear and the in-
state spending of out-of-state visitors. All of these fisheries activities rely on fisheries
resources and habitats, and whereas future uses may impact these resources, existing
activities and trends, including fishing and other uses of the area, are already having an
impact on fisheries resources in the Ocean SAMP area. Human activities such as fisheries
that have been taking place for hundreds of years have influenced Ocean SAMP area
resources, and conditions in the area will continue to change due to human uses, such as
fishing, as well as longer-term trends such as global climate change.
5. It is acknowledged that future uses of the Ocean SAMP area may have a variety of
potential effects on fisheries resources and activities. See Chapter 8, Renewable Energy
and Other Offshore Development for a discussion of the potential effects of renewable
energy on fish and fisheries, and see Chapter 9, Other Future Uses for a discussion of
other future uses and their potential effects on fish and fisheries. In addition it should be
noted that future projects will be subject to site- and project-specific regulatory review to
evaluate the potential effects; see Section 560, Policies and Standards, for further
information.
6. While the emphasis of this chapter is on the commercial and recreational fisheries of the
state of Rhode Island and their importance to the state, it is acknowledged that fish and
fishing activities are not limited to state boundaries. Fishermen from other states,
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including Massachusetts, Connecticut, and New York, routinely transit through or fish
within the Ocean SAMP boundary area. The fish species found in the Ocean SAMP area
and the fishing activity that occurs here are undoubtedly of economic and cultural
importance to these other states as well, and any impacts to fisheries resources and
activities within the Ocean SAMP area could affect fishermen in other states. While the
remainder of this chapter is primarily focused on the importance of fisheries to the state
of Rhode Island, it is acknowledged that fishermen from outside of the state rely on these
resources as well.
7. While this chapter is focused on commercial and recreational fisheries, it is
acknowledged that the finfish, shellfish, and crustacean populations targeted by
fishermen are fundamental parts of the Ocean SAMP ecosystem. These species rely on
the availability of appropriate habitats and food sources, and the viability of these
fisheries is dependent upon these resources. In addition, there are numerous finfish,
shellfish, and crustacean populations within the Ocean SAMP area that are not part of
directed fisheries. See Chapter 2, Ecology of the Ocean SAMP Region for an extensive
discussion of the Ocean SAMP ecosystem, including other species, benthic habitat, and a
discussion of broader and longer-term regional trends. It is also acknowledged that global
climate change is having, and will continue to have, effects on fisheries resources and
activities; see Chapter 3, Global Climate Change for further discussion.
8. Commercial and recreational fisheries are discussed together in this chapter, although it is
acknowledged that there are significant differences between the commercial and
recreational industries. Commercial and recreational fisheries are included together
primarily because commercial and recreational fishermen target many of the same
species. Recreational fisheries here include recreational anglers as well as recreational
fishing that takes place aboard party and charter boats operated by professional captains
running businesses. It should be noted that recreational fishing is a significant
recreational activity and major contributor to Rhode Island’s tourism economy; see
Chapter 6, Recreation and Tourism for further discussion.
9. Aquaculture is an activity that is relevant to seafood production and is currently permitted
only in state waters. Offshore aquaculture may be a potential future use of the Ocean
SAMP area once a federal permitting process is established. See Chapter 9, Other Future
Uses for further discussion.
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Section 510. Marine Fisheries Resources in the Ocean SAMP Area
510.1. Species Included in this Chapter
510.1.1. Species Important to Commercial and Recreational Fisheries
1. This chapter’s focus is on commercial and recreational fisheries, finfish, shellfish, and
crustacean species that are considered most important to Rhode Island commercial and
recreational fishermen operating in the Ocean SAMP area. Lists of commercially and
recreationally important species were developed through the methodology outlined
below and resulted in a summary list of species included below in Table 5.1.
2. Species harvested within the Ocean SAMP area that are considered to be most important
to Rhode Island’s commercial fisheries were identified by reviewing NMFS landings
data and then reviewing this draft list with Rhode Island commercial fisheries
stakeholders. Ten years (1998 – 2007) of NMFS landings data were reviewed to
determine the most valuable finfish, shellfish, and crustacean species landed in Rhode
Island (NMFS 2009a). For each year, the top 20 species (ranked by value) were
identified. This list was then edited down to those species which occurred in the top 20
(by value) in at least 5 of those 10 years. This list was then reviewed with commercial
fishermen to determine which species are actually harvested within the Ocean SAMP
area. This review took place during fisheries stakeholder meetings conducted through the
Ocean SAMP stakeholder process. Through this process, most shellfish were removed
from this list, with the exception of sea scallops, which are harvested within the Ocean
SAMP area. It should be noted that while quahogs are well known to be an important and
lucrative fishery in Rhode Island, quahogs are currently harvested primarily within
Narragansett Bay, not offshore in the Ocean SAMP area, and are therefore not included
here. The species identified through this process are: American lobster (Homarus
americanus); Atlantic cod (Gadus morhua); Atlantic herring (Clupea harengus); Atlantic
mackerel (Scomber scombrus); Atlantic sea scallop (Placopecten magellanicus); Black
sea bass (Centropristis striata); Butterfish (Peprilus triacanthus); Goosefish (monkfish)
(Lophius americanus); Longfin (loligo) squid (Loligo pealeii); Scup (Stenotomus
chrysops); Silver hake (Merluccius bilinearis); Skates (unclassified); Summer flounder
(Paralichthys dentatus); Winter flounder (Pseudopleuronectes americanus); and
Yellowtail flounder (Limanda ferruginea). The above list was then compared with those
commercially harvested species managed at the state level with quotas or other daily
landing limits (RIDEM 2009), to ensure any significant species managed at the state
level were accounted for. Because they appear on this list, and in addition are both found
within the Ocean SAMP area, two additional species, menhaden (Brevoortia tyrannus)
and spiny dogfish (Squalus acanthias), are included in this chapter.
3. Species important to recreational fisheries were identified by reviewing Rhode Island
recreational harvest and release data published in Fisheries Economics of the United
States, 2006 (NMFS 2008a).2 This list was then compared with RI Department of
Environmental Management recreational fishing regulations (RIDEM 2009), as well as
information on sportfishing tournaments sponsored by the RI Saltwater Anglers
2 This is the most recent version of this publication available.
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Association (RISAA 2010). The resultant draft list of species was then reviewed with
both recreational anglers and party and charter boat fishermen with the goal of
determining which species are actually targeted within the Ocean SAMP area. This
review took place during fisheries stakeholder meetings conducted through the Ocean
SAMP stakeholder process. The species identified through this process are: Atlantic
bonito (Sarda sarda); Atlantic cod (Gadus morhua); Black sea bass (Centropristis
striata); Bluefish (Pomatomus saltatrix); False albacore (Euthynnus alletteratus); Scup
(Stenotomus chrysops); Sharks (unspecified); Striped bass (Morone saxatilis); Summer
flounder (Paralichthys dentatus); Tautog (Tautoga onitis); Tunas (unspecified); and
Winter flounder (Pseudopleuronectes americanus). Recreationally targeted sharks were
further narrowed down to Shortfin mako (Isurus oxyrinchus), Blue (Prionace glauca),
and Thresher (Alopias vulpinus), and recreationally targeted tunas were further narrowed
down to Bluefin (Thunnus thynnus) and Yellowfin (Thunnus albacares). It should be
noted that the species that appear on the list below may also be of commercial and
recreational importance to fishermen from other states fishing in the Ocean SAMP area,
or may migrate to other areas where these fish may be targeted by non-Rhode Island
fishermen.
4. Table 5.1 shows the resultant list of commercially and recreationally important species
found within the Ocean SAMP area:
Table 5.1. Commercially and recreationally important species.
Common Name
Scientific Name
American lobster
Homarus americanus
Atlantic bonito
Sarda sarda
Atlantic cod
Gadus morhua
Atlantic herring
Clupea harengus
Atlantic mackerel
Scomber scombrus
Atlantic sea scallop
Placopecten magellanicus
Black sea bass
Centropristis striata
Bluefish
Pomatomus saltatrix
Butterfish
Peprilus triacanthus
False albacore
Euthynnus alletteratus
Goosefish (monkfish)
Lophius americanus
Longfin (loligo) squid
Loligo pealeii
Menhaden
Brevoortia tyrannus
Scup
Stenotomus chrysops
Shark, blue
Prionace glauca
Shark, shortfin mako
Isurus oxyrinchus
Shark, thresher
Alopias vulpinus
Silver hake
Merluccius bilinearis
Skates (unclassified)3
Raja spp.
Spiny dogfish
Squalus acanthias
Striped bass
Morone saxatilis
Summer flounder
Paralichthys dentatus
Tautog
Tautoga onitis
3 Skates are listed as unclassified by NMFS because they are often landed as a mix of species, with Little Skate as
the predominant species
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Tuna, bluefin
Thunnus thynnus
Tuna, yellowfin
Thunnus albacares
Winter flounder
Pseudopleuronectes americanus
Yellowtail flounder
Limanda ferruginea
5. The commercially and recreationally important species identified above are managed by a
variety of different federal and state management entities. Table 5.2 below includes a
summary of the relevant management entities for each species as well as the current
status of each stock as of March 2010. As defined in the Magnuson Stevens Fishery
Conservation and Management Act, 16 U.S.C. 1801 et. seq. (Magnuson Stevens Act),
“the terms ‘overfishing’ and ‘overfished’ mean a rate or level of fishing mortality that
jeopardizes the capacity of a fishery to produce the maximum sustainable yield on a
continuing basis” (NMFS 2007c). This information is summarized from the individual
species descriptions that follow below in Section 510.2, which include further details and
references for each species.
Table 5.2. Management and status of species/stocks in the Ocean SAMP area.
Common name
Management entity
Status of stock within Ocean
SAMP area as of March 2010
American
lobster
Atlantic States Marine Fisheries Commission
Depleted; overfishing not
occurring
Atlantic bonito
International Commission for the Conservation of
Atlantic Tunas
Not available
Atlantic cod
New England Fishery Management Council
Overfished; overfishing is
occurring
Atlantic herring
Atlantic States Marine Fisheries Commission and
New England Fishery Management Council
Not overfished; overfishing not
occurring
Atlantic
mackerel
Mid-Atlantic Fishery Management Council
Not overfished; overfishing not
occurring
Atlantic sea
scallop
New England Fishery Management Council
Not overfished; overfishing not
occurring
Black sea bass
Atlantic States Marine Fisheries Commission and
Mid-Atlantic Fishery Management Council
Not overfished; overfishing not
occurring
Bluefish
Atlantic States Marine Fisheries Commission and
Mid-Atlantic Fishery Management Council
Not overfished; overfishing not
occurring
Butterfish
Mid-Atlantic Fishery Management Council
Pending release of 2009 NMFS
stock assessment
False albacore
International Commission for the Conservation of
Atlantic Tunas
Not available
Goosefish
(monkfish)
New England Fishery Management Council; Mid-
Atlantic Fishery Management Council
Not overfished; overfishing is
occurring
Longfin (loligo)
squid
Mid-Atlantic Fishery Management Council
Not overfished; overfishing not
occurring
Menhaden
Atlantic States Marine Fisheries Commission
Not overfished; overfishing not
occurring
Scup
Atlantic States Marine Fisheries Commission and
Mid-Atlantic Fishery Management Council
Not overfished; overfishing not
occurring
Shark, blue
National Marine Fisheries Service (Consolidated
Atlantic Highly Migratory Species Fishery
Management Plan); Atlantic States Marine
Not available
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Fisheries Commission (Interstate Fishery
Management Plan for Atlantic Coastal Sharks)
Shark, shortfin
mako
National Marine Fisheries Service (Consolidated
Atlantic Highly Migratory Species Fishery
Management Plan); Atlantic States Marine
Fisheries Commission (Interstate Fishery
Management Plan for Atlantic Coastal Sharks)
Not overfished; overfishing is
occurring
Shark, thresher
National Marine Fisheries Service (Consolidated
Atlantic Highly Migratory Species Fishery
Management Plan); Atlantic States Marine
Fisheries Commission (Interstate Fishery
Management Plan for Atlantic Coastal Sharks)
Not available
Silver hake
New England Fishery Management Council
Not overfished; overfishing not
occurring
Skates
(unclassified)
New England Fishery Management Council
Overfishing occurring on winter
skate only
Spiny dogfish
Atlantic States Marine Fisheries Commission;
New England Fishery Management Council; Mid-
Atlantic Fishery Management Council
Not overfished; overfishing not
occurring
Striped bass
Atlantic States Marine Fisheries Commission
Not overfished; overfishing not
occurring
Summer
flounder
Atlantic States Marine Fisheries Commission and
Mid-Atlantic Fishery Management Council
Not overfished; overfishing not
occurring
Tautog
Atlantic States Marine Fisheries Commission
Overfished; overfishing is
occurring
Tuna, bluefin
National Marine Fisheries Service (Highly
Migratory Species Fishery Management Plan) and
International Commission for the Conservation of
Atlantic Tunas
Overfished; overfishing is
occurring
Tuna, yellowfin
National Marine Fisheries Service (Highly
Migratory Species Fishery Management Plan) and
International Commission for the Conservation of
Atlantic Tunas
Not overfished; overfishing not
occurring
Winter flounder
Atlantic States Marine Fisheries Commission and
New England Fishery Management Council
Overfished; overfishing is
occurring
Yellowtail
flounder
New England Fishery Management Council
Overfished; overfishing is
occurring
510.1.2. Forage Fish
1. Forage fish are essential to a discussion of commercial and recreational fisheries insofar
as they provide food for many of the above-mentioned targeted species. Many forage fish
in this region are themselves commercially or recreationally targeted. See Section 510.4
for a brief discussion of forage fish as they relate to the above-mentioned species.
510.1.3. Threatened and Endangered Species and Species of Concern
1. This chapter also includes discussion of Threatened and Endangered finfish per the
Endangered Species Act (16 U.S.C. 1531 et. seq.) as well as finfish listed as “Species of
Concern” by the NMFS Office of Protected Resources. According to the NMFS
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Northeast Regional Office Protected Resources Division, based on the best available
information, no finfish currently listed as threatened or endangered are likely to occur
within the Ocean SAMP area (J. Crocker, pers. comm., a). However, according to the
NMFS Northeast Regional Offices Protected Resources Division (J. Crocker, pers.
comm., b), the following species currently listed as “Species of Concern” could be
present in the Ocean SAMP area: Alewife (Alosa pseudoharengus); Atlantic halibut
(Hippoglossus hippoglossus); Atlantic sturgeon (Acipenser oxyrinchus oxyrinchus);
Atlantic wolffish (Anarhichas lupus); Blueback herring (Alosa aestivalis); Dusky shark
(Carcharhinus obscurus); Porbeagle shark (Lamna nasus); Rainbow smelt (Osmerus
mordax); Sand tiger shark (Carcharias taurus); and Thorny skate (Amblyraja radiate).4 It
should also be noted that Atlantic sturgeon are currently a candidate species for listing
under the Endangered Species Act (NMFS 2010a). Accordingly, these species are
included in this chapter and are discussed in detail in Section 510.5.
4 See the NOAA NMFS Office of Protected Resources for a complete list of designated “Species of Concern”:
http://www.nmfs.noaa.gov/pr/species/concern/.
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510.2. Life History, Habitat, and Fishery of Commercially and Recreationally Important Species
510.2.1. American Lobster (Homarus americanus)
1. The American lobster is a bottom-dwelling crustacean widely distributed over the North
American continental shelf, occurring inshore in the U.S. from Maine through New
Jersey, and offshore from Labrador, Canada through North Carolina (ASMFC 2008a). In
the Ocean SAMP area, American lobsters are targeted by commercial fishermen.
Life History
2. Lobsters are long-lived, and grow incrementally through molting. During the first two
years of their lives, lobsters will molt several times each year, and once or twice per year
thereafter, depending on food availability and water temperature (ASMFC 2008a). Most
lobsters molt in July or August; with each molt the lobster increases 14% in length and
50% in weight. Lobsters reach legal size in about five to seven years, depending on water
temperature (ASMFC 2008a). In Rhode Island, minimum legal size is currently 33/8
inches in carapace length.
3. Lobsters become sexually mature between their fifth and eighth year, and may molt as
many as 25 times before reaching adulthood (Lobster Conservancy 2004). Female
lobsters mate immediately after molting, and store the sperm for up to two years until
they extrude their eggs, which are then fertilized. Females carry eggs on their underside
for nine to eleven months before hatching. Eggs hatch from mid-May through mid-June
(ASMFC 2008a). For the first two months of their lives, lobsters are planktonic, floating
at the surface before they sink to the bottom. During their planktonic stage, lobsters
sometimes travel great distances and may settle far from their source. Studies of lobster
populations have found in some cases only a small percentage of new recruits have come
from within the population, and in some cases the percentage of self-recruitment (larvae
settling back into the same population) is more than 90 percent. Sources and sinks of
larvae will vary from year to year depending on factors such as wind and currents (e.g.
Incze et al. 2010). During the first year of their lives, lobsters remain within a meter (3.3
feet) of the spot where they settled (Wahle 1992).
Habitat
4. Lobsters are solitary and territorial. They are most abundant in shallow coastal areas, and
are concentrated in rocky habitat where shelter is available, particularly among cobbles
and boulders, but also occur in offshore waters. In Rhode Island, lobsters are most often
found close to shore among rocks, but they will also frequently burrow in featureless
mud, particularly when shelter is not available (Cobb and Wahle 1994). Offshore lobsters
are most commonly found along submarine canyons on the edge of the continental shelf.
Inshore lobsters typically remain within a home range of about five to ten square
kilometers, although large, mature lobsters living in offshore areas will migrate inshore
seasonally in the spring and summer to reproduce (ASMFC 2008a). Lobsters in Rhode
Island will migrate into Narragansett Bay and other inshore areas during the summer, and
return to the Sounds during the fall, traveling as much as 136 nautical miles (252 km)
(Saila and Flowers 1968). Pelagic lobster larvae feed primarily on copepods and diatoms.
Adults are opportunistic feeders, feeding on fish, crabs, clams, mussels, and sea urchins,
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among other species. They are also cannibalistic, and will sometimes eat other lobsters
(Lobster Conservancy 2004).
Fishery
5. Three separate stocks of lobsters have been recognized: the Gulf of Maine, Georges
Bank, and Southern New England stocks. Lobsters are further divided into seven
management areas; Rhode Island waters fall within Management Area 2. Lobsters in
both state and federal waters are managed under the Interstate Fisheries Management
Program administered by the Atlantic States Marine Fisheries Commission. The fishery
is managed through size limits, trap limits, and the practice of cutting a notch in the tail
(v-notching) of egg-bearing females. Management measures also include regulations
dictating minimum wire gauge and escape vent sizes on the traps. The 2009 peer-
reviewed stock assessment report by the Atlantic States Marine Fisheries Commission
found overall record high stock abundance in the Gulf of Maine and Georges Bank
stocks. For the Southern New England stock, however, abundance is the lowest observed
since the 1980s, and recruitment is also very low, although exploitation rates have also
declined (ASMFC 2009a). The stock is listed as depleted but overfishing is not
occurring. There was a rebuilding program for Southern New England lobster established
in 2007; the stock is expected to be rebuilt by 2022 (ASMFC 2009a).5 According to the
University of Maine Lobster Stock Assessment model used by the Atlantic States Marine
Fisheries Commission technical committee, the recent abundance for Southern New
England lobster from 2005-2007 averaged 14.7 million, and the abundance threshold for
the stock is 25.4 million, making the stock overfished (ASMFC 2009a). The average size
of lobsters taken within the Southern New England area has been declining for both
males and females. NMFS reports there is an excess of effort in the lobster fishery for
Southern New England. States report a number of latent licenses which, if used, would
exacerbate the excess of effort (NOAA NMFS Northeast Fisheries Science Center
[NEFSC] 2006a). It is not well understood what the sources of new settlers to lobster
populations in the Ocean SAMP area might be, but it is important to note that this may
vary depending on climatic and oceanographic factors, and lobster populations in the
Ocean SAMP area may be determined somewhat by spawning and thus population trends
elsewhere.
Table 5.3. Habitat characteristics of American lobster. (ASMFC 2008a; ASMFC 2009a; Cobb and Wahle
1994)
Life Stage
Habitat
Substrate
Temperature
Eggs
Carried on underside of females for 9 to
11 months
N/A
N/A
Larvae
Larvae go through five stages, the first
four of which are planktonic. They sink
to the floor in the fifth stage
Mostly pelagic
N/A
Juveniles
Shallow, rocky habitats; areas with small
Cobble, boulders,
N/A
5 In this and all subsequent species descriptions, the terms “overfished” and “overfishing” are used to describe
species’ stock status. “Overfishing” is defined in the Magnuson-Stevens Act as fishing at a rate or rate or level of
mortality that jeopardizes the capacity of a fishery to produce the maximum sustainable yield on a continuing basis.
A stock is deemed “overfished” when the population size is determined to be less that that needed to sustain the
fishery. For further information see NMFS 2010b.
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shelter-providing spaces; less than 20m in
depth. Small juveniles and larvae may use
salt marsh peat reefs
subtidal peat,
rocky habitats
Adults
Coastal lobsters found in rocky areas,
sometimes burrow in mud substrates;
offshore lobsters found along edge of
continental shelf near submarine canyons
Cobble,
sometimes mud or
sand
-2 – 24ºC; generally
inactive below 4ºC
510.2.2. Atlantic Bonito (Sarda sarda)
1. The Atlantic bonito, also called the skip jack, is an open-ocean fish found in temperate
and tropical waters on both sides of the Atlantic. It is common along the east coast of the
United States north to Cape Cod. The bonito is in the family Scombridae with tunas and
mackerels, and is shaped like a small tuna. In the Ocean SAMP area, bonito are targeted
by recreational fishermen.
Life History
2. Most bonito reach sexual maturity at two years of age, although some become sexually
mature after their first year. Fecundity for females increases with age and size; large
females can produce as many as three to six million eggs. Spawning usually occurs to the
south of New England during the summer. Juveniles grow nearly a tenth of an inch (0.3
cm) per day in their first summer. Bonito are generally daytime feeders, feeding mostly
in the morning and the evening, and sometimes leaping out of the water in large numbers
while chasing prey. They can swim up to 30 or 40 miles (48 to 64 km) per hour in pursuit
of prey (Ross 1991).
Habitat
3. The bonito is a schooling fish found in the open waters off the continental shelf, normally
at depths of less than 200 meters (656 feet). Bonito prefer temperatures between 54 and
77 degrees Fahrenheit (12 and 25 degrees Celsius), and are most abundant at
temperatures between 59 and 72 degrees (15 and 22 degrees Celsius). Bonito are found
offshore off southern New England in the summer and fall, and migrate south for the rest
of the year. Although they are usually an open-ocean species, they are sometimes found
near the coast. Larval bonito feed on copepods and small fish larvae, while juveniles and
adults eat squid and a number of fish including mackerel, alewives, menhaden, sand
lance, silversides, and smaller bonito (Ross 1991).
Fishery
4. Bonito are targeted primarily as a recreational species, and are known for being fast and
powerful. They are managed internationally through the International Commission for
the Conservation of Atlantic Tunas (ICCAT). At present, there is no Fishery
Management Plan in place for bonito; recreational anglers are not required to have a
permit to fish for bonito. There are no size or bag limits for bonito.
Table 5.4. Habitat characteristics of Atlantic bonito. (Ross 1991)
Life Stage
Habitat
Substrate
Temperature
Juveniles/Adults
Open ocean species, usually in
waters less than 200 m deep.
Open ocean
From 12 to 25ºC, most abundant
between 15 and 22ºC.
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510.2.3. Atlantic Cod (Gadus morhua)
1. Cod are found on both sides of the Atlantic, and range from Greenland to North Carolina
in the Northwest Atlantic. Cod are assessed by NMFS as two separate stocks; one in the
Gulf of Maine, and the other found on Georges Bank and Southward. Cod are targeted in
the Ocean SAMP area by both commercial and recreational fishermen.
Life History
2. Cod typically move south and into deeper water in the winter and spring. The cod found
in southern New England waters are probably part of a stock that migrates from
Nantucket Shoals in the summer to waters off New Jersey and North Carolina in the
winter where they spawn. The cod’s eggs and larvae are pelagic for the first three or four
months. In 1972, the median age of maturity on Georges Bank was found to be 2.9 years
for females and 2.6 years for males, with the median size of both being around 50 cm (20
inches) at maturity. Studies have found significant declines in the median age and size at
maturity resulting from declining stock abundance and changes in temperature (Collette
and Klein-MacPhee 2002). The fecundity of females increases with age and size. The
largest codfish ever recorded was caught off Massachusetts in 1895, weighing 96 kg
(211.6 pounds) and measuring 183 cm (72 inches) in length. Cod weighing between 23-
27 kg (51 - 60 pounds) are not unusual, but most commercially taken cod weigh only
between 2.5 and 4.0 kg (5.5 and 9 pounds) (Collette and Klein-MacPhee 2002). Cod can
reach a maximum of 26 to 29 years of age (Collette and Klein-MacPhee 2002).
Habitat
3. Cod are a bottom-dwelling fish, preferring rocky, pebbly, or sandy bottoms, and prefer
temperatures between 32 and 50 degrees Fahrenheit (0 to 10 degrees Celsius), although
they are often found on Nantucket Shoals in water temperatures as high as 59 degrees
Fahrenheit (15 degrees Celsius) (Collette and Klein-MacPhee 2002). They can be found
at depths of up to 1200 feet (366 meters), but more typically are found at depths between
200 to 360 feet (60 to 110 meters) (Ross 1991). In Rhode Island waters, cod can be found
in shallow coastal waters from October through mid-May, and year-round on Cox Ledge.
Cod spawn in the Gulf of Maine, Georges Bank, and southern New England. During
their first year, cod are often found in shallow waters close to shore or on Nantucket
Shoals and other shallow banks (Collette and Klein-MacPhee 2002).
4. Cod will feed on many different kinds of fish and invertebrates, but especially herring,
sand lance, Atlantic mackerel, squids, silver hake, and rock crabs (Collette and Klein-
MacPhee 2002). Juveniles eat mostly small crustaceans, while larvae feed on copepods
and phytoplankton (Collette and Klein-MacPhee 2002). Juvenile cod are themselves prey
for pollock, squid, spiny dogfish, sea ravens, and larger cod (Ross 1991), while adults are
preyed upon by large sharks and dogfish (Collette and Klein-MacPhee 2002), as well as
seals (Ross 1991).
Fishery
5. The Georges Bank and Southward stock supports a commercial fishery year round, and a
recreational fishery from late autumn to early spring. Cod are managed by the New
England Fishery Management Council as part of the fifteen species Northeast
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Multispecies Fishery Management Plan, through a combination of time/area closures,
gear restrictions, and minimum size limits, as well as moratoriums on permits and days-
at-sea restrictions. Commercial landings of the Georges Bank and Southward stock hit a
record low in 2005, and the stock remains below the long-term average. Fishing
mortality has been declining since 1997, but spawning stock biomass (SSB) has also
been declining since 2001. The National Marine Fisheries Service defines spawning
stock biomass as: “the total weight of all sexually mature fish in the population. This
quantity depends on year class abundance, the exploitation pattern, the rate of growth,
fishing and natural mortality rates, the onset of sexual maturity and environmental
conditions.” (NEFSC n.d.). The 2004 SSB was at 10% of the SSB needed for maximum
sustainable yield. The stock is thus considered overfished, and overfishing is currently
occurring, meaning fishing is occurring at a rate that jeopardizes the ability of the stock
to produce maximum sustainable yield (NEFSC 2006a). However, the Georges Bank and
Southward stock is currently in the process of being rebuilt, and as of 2009 the Gulf of
Maine stock is no longer considered overfished (NMFS 2010b).
Table 5.5. Habitat characteristics of Atlantic cod. (Northeast Fisheries Science Center [NEFSC] 2004a)
Life Stage
Habitat
Substrate
Temperature
Eggs
Bays, harbors, offshore banks. Usually < 70 m.
Pelagic
Most 2.0-8.5ºC for
incubation.
Larvae
Most over Georges Bank, perimeter
of Gulf of Maine, southern New England,
continental shelf. Densest in spring. Youngest
from surface to 75 m. Move deeper with age.
Migrate vertically in reaction to light.
Pelagic
Most 4-8ºC in winter -
spring, 7-12ºC in
summer-fall.
Juveniles
Mostly in shallow waters, coastal or offshore
banks, during summer. Deeper water in winter.
‘Cobble’ preferred
over finer grains.
Uses vegetation
for predator
avoidance.
6 - 20ºC.
More tolerant of
extremes than adults.
Adults
Seasonal migrations except in Gulf of Maine.
Most dense Massachusetts Bay, northeast Georges
Bank, Nantucket Shoals. Usually on bottom
during day, may move up into water column at
night. Most found between 60 and 110 meters.
Rocky, pebbly,
gravelly. Avoid
finer sediments.
Generally < 10ºC,
varies seasonally.
510.2.4. Atlantic Herring (Clupea harengus)
1. Atlantic herring are pelagic species that occur in large schools, and inhabit coastal and
continental shelf waters from Labrador to Virginia. The commercial fishery for herring in
New England developed in the late 19th century as the canning industry was developing.
An extensive foreign fishery developed on Georges Bank in the 1960s, leading to a
collapse of the offshore herring stock. Today, the herring stock is completely rebuilt.
Herring are often canned, or sometimes processed as frozen or salted fish by foreign
ships that purchase the fish from U.S. fishermen and processing plants. Herring are also
commonly used as bait in the lobster fishery, as well as the blue crab and tuna fisheries.
Because of their importance as a forage species, they also have an important indirect
value for whale watching and other ecotourism industries (ASMFC 2008a). In the Ocean
SAMP area, herring are targeted primarily by commercial fishermen.
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Life History
2. Herring usually spawn during the fall months, producing anywhere from 30,000 to
200,000 eggs each. Eggs will hatch in ten to twelve days depending on the water
temperature, and the hatchlings are about a quarter inch (0.6 cm) long. In the spring, the
larvae will transform into juveniles, about an inch and a half long (4 cm). They will grow
three to five inches (7 to 13 cm) the next fall, reaching ten inches (25 cm) and sexual
maturity by their fourth year, and can grow up to about fifteen inches (38 cm) in fifteen
to eighteen years (ASMFC 2008a). Herring may live twenty years or longer (Collette and
Klein-MacPhee 2002).
Habitat
3. Juvenile herring, which are commonly called sardines, migrate from shallow, inshore
waters during the summer to deeper, offshore waters during the winter months. Adult
fish older than three years will migrate from their spawning grounds in the Gulf of Maine
and Georges Bank to spend the winter months in southern New England and the Mid-
Atlantic. Herring will spawn during October and November in the southern Gulf of
Maine, Georges Bank, and Nantucket Shoals. They prefer rock, gravel, or sand bottoms
between 50 feet and 150 feet (15 and 45 m) in depth for spawning (ASMFC 2008a).
4. Herring are filter feeders and feed on plankton, primarily copepods. They usually feed at
night, following the zooplankton that inhabit deeper waters during the day and traveling
to the surface to feed at night (ASMFC 2008a). Herring themselves play a very important
role in the ecosystem, as they are a significant source of food for many species of fish,
including cod, haddock, silver hake, striped bass, bluefish, monkfish, mackerel, tuna, and
spiny dogfish, as well as birds and marine mammals (Collette and Klein-MacPhee 2002).
Fishery
5. Atlantic herring are managed by the Atlantic States Marine Fisheries Commission in
state waters, and by the New England Fishery Management Council in federal waters.
Herring is not currently considered overfished, and overfishing is not occurring at
present. Fishing mortality has been low since the early 1990s. In 2007, the New England
Fishery Management Council implemented a mid-water trawl ban on herring between
June 1 and September 30, but no ban exists in state waters. Herring are managed based
on a Total Allowable Catch (ASMFC 2008a). Read and Brownstein (2003) found the rate
of consumption of herring by marine mammals to greatly exceed the total estimated
rates of natural mortality of the species within the Gulf of Maine currently used in stock
assessments, and predicted that as marine mammal populations increase, the
consumption of herring will likewise increase. These trophic interactions may have not
been sufficiently considered in stock assessment models for this species.
Table 5.6. Habitat characteristics of Atlantic herring. (NEFSC 2005a)
Life Stage
Habitat
Substrate
Temperature
Eggs
Discrete, demersal, egg “beds” in coastal
waters and on offshore banks and ledges
in the Gulf of Maine and on Georges
Bank with strong bottom currents and
coarse substrate, depths of 5-90 m
Boulders, rocks,
gravel, coarse
sand, shell
fragments,
macrophytes, and
on a variety of
Bottom temperatures
over egg beds ranged
from 7-15ºC; egg
development normal
1-22ºC; development
rates/ incubation
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benthic organisms
and man-made
structures (e.g.,
lobster traps); not
on mud or fine
sand.
times inversely
related to temperature
Larvae
Estuaries, coastal, and offshore waters
between Bay of Fundy and New Jersey;
remain on or near bottom for first few
days after hatching, then rise to surface
and are dispersed by currents. Depths
from very shallow waters to 200 m; most
50-90 m
Pelagic
Lab study shows
larvae tolerate wide
temperature range (-
1.8 to 24ºC).
Juveniles
One-year-olds in nearshore waters during
summer and fall, overwinter in deeper,
coastal waters; two-year-olds in
inshore/offshore continental shelf waters
of Gulf of Maine, deeper waters of
Georges Bank in summer and fall, Cape
Hatteras to deeper parts of Georges Bank
in winter, widespread from Cape Hatteras
to Bay of Fundy in spring. Mostly < 100
m in spring; migrate up in water column
at dusk and down at dawn.
Pelagic
Prefer 8-12ºC
Adults
Pelagic, but spawn on bottom;
inshore/offshore continental shelf waters
of the Gulf of Maine and deeper parts of
Georges Bank in summer and fall, Cape
Hatteras to deeper parts of Georges Bank
in winter, distributed across shelf in mid-
Atlantic, southern New England, deeper
waters of Georges Bank, and the
southwest portion of the Gulf of Maine in
spring.
Pre-spawning
aggregations more
abundant over
gravel/sand.
Field observations
suggest adults prefer
5-9ºC on Georges
Bank in summer/ fall;
most caught 4-7ºC in
spring and 6-10ºC in
fall NEFSC trawl
surveys
510.2.5. Atlantic mackerel (Scomber scombrus)
1. The Atlantic mackerel is a pelagic fish found from the Gulf of St. Lawrence to Cape
Hatteras. There are two separate stocks of mackerel, one of which spends winters
between the Chesapeake Bay and Long Island, and moves northward along the New
England coast in June and July, and the other which moves inshore to southern New
England in late May, and migrates north toward Nova Scotia (Ross 1991). In the Ocean
SAMP area, mackerel are targeted both by commercial and recreational fishermen.
Life History
2. Adult mackerel usually measure about fourteen to eighteen inches (35 to 46 cm) in length
and weigh about a pound (0.5 kg). They are generally found in Rhode Island waters from
May through September, and migrate offshore to the edge of the continental shelf in
winter. They spawn in the Mid-Atlantic Bight and in the Gulf of Maine in spring and
early summer, once the water is warmer than 46 degrees Fahrenheit (8 degrees Celsius)
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(Collette and Klein-MacPhee 2002). The fish will form schools when they are about 40
days old, and are about two inches long (5 cm). The mortality rates of young mackerel
are very high (Ross 1991). Mackerel grow to about eight inches (20 cm) by the end of
their first year, and are sexually mature by their second year (Collette and Klein-
MacPhee 2002).
Habitat
3. Mackerel are found in dense schools between 100 fathoms (183 meters) and the surface.
They are an open-ocean fish often found over the edge of the continental shelf, but will
also inhabit brackish coastal waters. They prefer to spawn near the surface. Mackerel are
opportunistic feeders, and feed largely on zooplankters, including copepods, shrimps, and
fish larvae. Larger mackerel will feed on larger prey such as squid, silver hake, sand
lance, herring, and sculpins (Collette and Klein-MacPhee 2002). They are an important
prey species for whales, porpoises, sharks, cod, tunas, bluefish, striped bass, birds, and
squid, which eat small mackerel (Ross 1991).
Fishery
4. Mackerel are an important species for both commercial and recreational fisheries. The
Atlantic mackerel stocks are currently managed by the Mid-Atlantic Fishery
Management Council under the Atlantic Mackerel, Squid, and Butterfish Fishery
Management Plan. Spawning stock biomass for mackerel has increased steadily since
1976, and fishing mortality has been low since 1992 (NEFSC 2006a). Spawning biomass
reached a record high in 2004, and population estimates put biomass of Atlantic mackerel
at 257% above what is needed to support maximum sustainable yield (NMFS 2010b).
Thus, the stock is not overfished and overfishing is not considered to be occurring
(NEFSC 2006a).
Table 5.7. Habitat characteristics of Atlantic mackerel. (NEFSC 1999a)
Life Stage
Habitat
Substrate
Temperature
Eggs
Highest abundances in May/June in
southern New England - Mid-Atlantic
region. Eggs pelagic, distributed at depths
ranging from 10-325 m, majority from 30-
70 m.
Pelagic
Eggs collected at 5-23ºC,
highest abundance from ~
7-16ºC with range related to
season.
Larvae
Highest abundance ranges from Hudson
Canyon north to southern New England and
north of Cape Cod. Most distributed at
depths from 10-130 m, usually at < 50 m.
Pelagic
Larvae collected at 6-22ºC;
highest abundance at 8-
13ºC.
Juveniles
Late summer/fall primarily along western
shores of Gulf of Maine, inshore areas of
New England (includes estuaries in Rhode
Island, Connecticut, eastern Long Island).
Depth varies seasonally. Offshore in fall,
most abundant at ~ 20-40 m, range from 0-
320 m. In winter, 50-70 m. Spring, although
dispersed through water column,
concentrated 30-90 m. Move higher in
summer to 20-50 m, range from 0-210 m.
Pelagic
Temperature distribution
offshore changes seasonally
as average temperature
ranges increase: in Rhode
Island, 19ºC in summer, 11
and 15ºC in fall.
Adults
Fall: concentrated at 60-80 m. Winter: ~
Pelagic
Offshore distribution varies
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50% at 20-30 m. Spring: down to 380 m.
Summer: > 60% at 50-70 m. Larger fish
deeper than smaller ones. Distribution may
also be correlated with downwelling events
and onshore advection of warm surface
water. Found on edge of continental shelf,
but will also inhabit brackish waters. Most
spawning in shoreward half of continental
shelf, some on shelf edge and beyond.
with seasonal temperature
changes. Most found
between 5-14ºC. Spawning
begins when temperatures
are ~ 7ºC
(peak 9-14ºC) and
progresses from southern to
northern waters during adult
migration.
510.2.6. Atlantic Sea Scallop (Placopecten magellenicus)
1. The Atlantic sea scallop is found from the Gulf of St. Lawrence to Cape Hatteras. In the
Ocean SAMP area, sea scallop are harvested by commercial fishermen. The scallop
fishery is presently the most lucrative fishery in New England.
Life History
2. Sea scallops become sexually mature at age two, but those less than four years of age
probably contribute little to egg production. Fertilization takes place externally, and sea
scallops usually spawn in late summer and early autumn. A single female may release
hundreds of millions of eggs annually (NEFSC 2006a). Larvae remain in the water
column as part of the plankton for over one month after hatching (Pogsay 1979), during
which time eggs and larvae are subjected to currents. The spat, or juvenile larvae,
eventually sink and seek out hard substrate, such as shell fragments, on which to settle.
Young adults are exceptionally vulnerable to smothering by moving sands and loose
bottom substrates (Mullen and Moring 1986). Sea scallops grow rapidly, increasing their
shell height by 50 to 80 percent between ages three and five, and quadrupling their meat
weight. They reach commercial size at about four or five years of age. Sea scallops can
live up to 20 years. A combination of low mobility, rapid growth, and low natural
mortality means sea scallop populations grow rapidly in areas which are closed to fishing
activity (NEFSC 2006a).
Habitat
3. Sea scallops are found from mean low water to depths of several hundred feet. They are
found on a variety of bottom types, including firm sand, gravel, shells, and rocks (NEFSC
2004b). They prefer sand and gravel sediments, and water temperatures below 68 degrees
Fahrenheit (20 degrees Celsius). South of Cape Cod and on Georges Bank, sea scallops
are usually found at depths between 25 and 200 meters (82 and 656 feet), with most
commercial concentrations found between 35 and 100 meters (115 and 328 feet) of depth.
Sea scallops are filter feeders, feeding mainly on phytoplankton, but also on
microzooplankton and detritus (NEFSC 2006a). Large adults do not migrate, but can
escape predators by clapping the two halves of their shells together in a rudimentary form
of swimming.
Fishery
4. The fishery for sea scallops is conducted year-round, usually with scallop dredges. The
sea scallop fishery is managed by the New England Fishery Management Council. Most
sea scallop fishing in the United States is done by vessels with limited access permits,
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which provide them with days-at-sea and a limited number of trips to former closed
areas. Some sea scallop vessels have open access general category permits, allowing
them to take up to 400 pounds of meats per day; these are the vessels operating within
the Ocean SAMP waters. The biomass of sea scallops on Georges Bank was low from
1982 through 1994, but then increased, and has been at a high, stable level since 2000.
Surveys for Georges Bank and Mid-Atlantic sea scallops indicated the species was near
its historical maximum biomass in 2005 (NEFSC 2006a). The biomass of Atlantic sea
scallops in 2006 was estimated at 166,000 metric tons of meats, about 52% above the
amount needed to produce maximum sustainable yield (NMFS 2010b). They are not
considered to be overfished, nor is overfishing occurring (NEFSC 2006a).
Table 5.8. Habitat characteristics of Atlantic sea scallop. (NEFSC 2004b)
Life Stage
Habitat
Substrate
Temperature
Eggs
Remain on sea floor
N/A
N/A
Larvae
In mixed areas, larvae distributed
evenly through water column; in
stratified areas, larvae aggregated
above pycnocline. Migrate vertically
in response to tidal, solar cues.
Larvae settle in areas of
gravelly sand, shell
fragments or on hydroids,
bryozoans and sponges;
select substrates covered
with a biofilm.
N/A
Juveniles
N/A
Mainly found on gravel,
small rocks, shells, and
among branching animals
and plants that permit
attachment of juveniles.
N/A
Adults
Wide distribution on offshore banks
and coastal waters from
Newfoundland to Cape Hatteras;
from low tide level to ~100 m line;
generally shallower in northern
populations.
Generally found in seabed
areas with firm sand, gravel,
shells and cobble substrate.
Typically abundant in areas
with low levels of inorganic
suspended particulates (fine
clay size particles).
Prefer water
temperatures
below 20ºC
510.2.7. Black Sea Bass (Centropristis striata)
1. Black sea bass are concentrated from Cape Cod to Cape Canaveral, Florida. There are
two distinct and overlapping stocks of black sea bass along the Atlantic coast. In the
Ocean SAMP area, black sea bass are targeted by both commercial and recreational
fishermen.
Life History
2. Black sea bass are protogynous hermaphroditic, beginning life as females and then
changing to males when they reach about nine to thirteen inches (23 to 33 cm) in length.
In the Mid-Atlantic, 38% of females will change sex between August and April, after
most of the fish have already spawned. Most black sea bass will produce eggs when they
first mature, although some are already males at this stage, and then the ovaries
eventually stop functioning as sperm production begins. Most fish will reverse sex before
they reach the age of six (ASMFC 2008a). In populations where the larger, older males
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are heavily fished, females may change sex at an earlier age than they would in
populations unaffected by fishing (Ross 1991).
3. The northern stock of black sea bass spawns off New England from mid-May until the
end of June (Ross 1991), and an average sized fish will produce roughly 280,000 eggs.
The eggs float in the water column, hatching a few days after fertilization. The larvae
will drift offshore until they grow to a half an inch (one cm) in length, at which point the
young sea bass will migrate inshore into estuaries, bays, and sounds (ASMFC 2008a).
Habitat
4. Black sea bass are a temperate reef fish, preferring water about 48 degrees Fahrenheit (9
degrees Celsius), and they prefer to inhabit rock bottoms near pilings, wrecks, and jetties.
They are found in inshore waters at depths of less than 120 feet (37 meters) in the
summer, and move offshore to deeper waters to the south during the winter (ASMFC
2008a). Larger adults are usually found in deeper waters than smaller individuals, and
larger adults typically begin their migration earlier than the younger adults and juveniles,
starting in August (Ross 1991). Juvenile sea bass migrate inshore and prefer sheltered
habitats such as submerged aquatic vegetation, oyster reefs, and man-made structures.
Juveniles feed primarily on benthic invertebrates such as shrimp, isopods, and
amphipods, while adults feed on rock and hermit crabs, squid, fish, and mollusks (Ross
1991).
Fishery
5. In Rhode Island, black sea bass are important as both a commercial and recreational
species. Both commercial and recreational landings are regulated under a quota system,
managed jointly by the Atlantic States Marine Fisheries Commission and the Mid-
Atlantic Fishery Management Council under the Summer Flounder, Scup, and Black Sea
Bass Fishery Management Plan, in which 51 percent of the quota is given to the
recreational fishery, and 49 percent to the commercial fishery. The commercial quota is
further divided up by state based on historical landings; Rhode Island fishermen are
given eleven percent of the total quota for this species. By contrast the recreational quota
is managed under a coastwide plan (ASMFC 2008a). Black sea bass is currently
considered rebuilt by the Atlantic States Marine Fisheries Commission and overfishing is
not occurring (ASMFC 2009b). Abundance of black sea bass had declined after 2003,
but has since increased, and the stock was declared rebuilt in 2009 by NMFS. In 2008,
biomass of black sea bass in the Mid-Atlantic was estimated to be 3% above the target
level (NMFS 2010b).
Table 5.9. Habitat characteristics of black sea bass. (NEFSC 2007)
Life Stage
Habitat
Substrate
Temperature
Eggs
Mostly at shallow depths; majority
around 30m
Pelagic
Mostly between temperatures
of about 10-25ºC
Larvae
Reported in high salinity coastal areas of
southern New England in August and
September, but are rarely reported in
estuaries. Most found at 30-50 m in July
– September.
Pelagic
Between temperatures of 11-
26ºC. Most larvae found at
about 15-19ºC in July, at 15-
20ºC in August, and in 17-
21ºC in September.
Juveniles
Most abundant in oceanic waters of
Shellfish beds,
9-12°C in spring, 10-22°C in
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estuaries. High numbers of juveniles in
Rhode Island Sound, Buzzards Bay, and
the tip of Long Island in the fall. Found in
Narragansett Bay. Between 1-35 m, with
the majority between 6-15 m. Most
nurseries are located at depths < 20 m.
seagrass beds,
rocky reefs,
wrecks, cobble
habitats, manmade
structures
fall, with most between 17-
21°C.
Adults
Structurally complex habitats with steep
depth gradients. Use a variety of man-
made habitats. Over wintering habitats in
the Mid-Atlantic Bight appear to occur at
depths between 60-150 m. Some fish may
also over winter in deep water (> 80 m)
off southern New England. Depth range
in spring from 1 -65 m, with most
between 6-25 m, and between depths of
6-20 m in fall. Larger fish found in
deeper water.
Structurally
complex habitats,
including rocky
reefs, cobble and
rock fields, stone
coral patches,
exposed stiff clay,
and mussel beds.
In spring, temperature range of
3-17°C, with the majority at
10-14°C. In fall, over a range
of approximately 8-22°C, with
the majority between 16-21°C.
In Narragansett Bay, summer
temperature range of 15-24ºC,
with peaks at 91-20ºC.
Potential over wintering
habitat may be defined by
bottom water temperatures >
7.5ºC.
510.2.8. Bluefish (Potamomus saltatrix)
1. Bluefish are a migratory, pelagic species found throughout much of the world’s
temperate, coastal regions. In the Ocean SAMP area, bluefish are pursued primarily by
recreational fishermen.
Life History
2. Bluefish live up to fourteen years, and may weigh upwards of 31 pounds (14 kg) and
measure at least 39 inches (one meter) in length. They reach sexual maturity at two years,
and spawn offshore between Massachusetts and Florida. Different groups of bluefish
spawn at different times of the year, with some spawning in spring, some in summer, and
some in fall throughout their range (ASMFC 2008a). Once the larvae hatch, they live in
surface waters and are carried by currents along the continental shelf. The survival of the
young fish is highly variable from year to year, depending on whether the prevailing
circulation patterns carry them inshore to suitable habitats (Ross 1991).
Habitat
3. Bluefish are found between Maine and Cape Hatteras, North Carolina during the summer
months, and between Cape Hatteras and Florida in the winter (ASMFC 2008a). Larger
fish will migrate further north than younger ones. The fish will begin arriving off the
southern New England coast in April and May; smaller fish usually arrive first. Adults
will leave the coastal areas again in October, when the water cools to 60 degrees
Fahrenheit (16 degrees Celsius) (Ross 1991). They prefer warmer waters of at least 57 to
60 degrees Fahrenheit (14 to 16 degrees Celsius) in summer (Collette and Klein-
MacPhee 2002). Bluefish migrate in large schools, each of which may cover tens of
square miles of ocean (ASMFC 2008a). They inhabit both inshore and offshore habitats,
with young-of-the-year fish often found in estuaries and river mouths (Ross 1991).
4. Bluefish are voracious predators, and will eat almost anything they can catch and
swallow. Bigelow and Schroeder (1953) called the bluefish, “the most ferocious and
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bloodthirsty fish in the sea,” although Ross (1991) notes this reputation is somewhat
exaggerated. They have very sharp teeth and can take large bites, meaning they can eat
larger prey (ASMFC 2008a). Common prey include schooling species such as squid,
menhaden, mackerel, herring, alewives, and sand eels, as well as scup and butterfish.
They usually feed in schools, pursuing fish into tidal rips or inshore shallows. They are
known to force schools of menhaden and other fish up on shore, leading to fish kills.
Juvenile bluefish will feed on polychaetes, shrimp, other small crustaceans, small
mollusks, and small fish. Bluefish are prey for blue sharks, mako sharks, tuna, and
billfish (Ross 1991).
Fishery
5. Bluefish are an important species for recreational fisheries, and are popular with anglers
because of their aggressive feeding habits. Recreational harvest averages about 35
million pounds (16 million kilograms) per year. Bluefish are also targeted commercially
with trawls, gillnets, haul seines, and pound nets. The species is managed jointly by the
Mid-Atlantic Fishery Management Council and the Atlantic States Marine Fisheries
Commission. The Atlantic States Marine Fisheries Commission and the Mid-Atlantic
Fishery Management Council allocate 83 percent of the resource to recreational fisheries
and 17 percent to commercial fisheries. The commercial fishery is managed through
state-by-state quotas based on historic landings, and the recreational fishery is managed
by a fifteen-fish bag limit. According to the Atlantic States Marine Fisheries
Commission, bluefish are not overfished, nor is overfishing presently occurring. Recent
data have shown a decreasing trend in fishing mortality and an increase in stock biomass
and population numbers (ASMFC 2008a). Bluefish biomass in the Atlantic Ocean is
estimated to be at 5% above the level needed to support maximum sustainable yield, and
was estimated at 139,500 metric tons in 2006. A nine-year rebuilding plan was
implemented in 2001, and the stock was declared rebuilt in 2009 (NMFS 2010b). Cycles
of high and low abundance of bluefish have been observed to be the converse of striped
bass abundance patterns, but no explanation for this phenomenon has been found
(NEFSC 2006b).
Table 5.10. Habitat characteristics of bluefish. (NEFSC 2006b)
Life Stage
Habitat
Substrate
Temperature
Eggs
Occurs across continental shelf, southern
New England to Cape Hatteras. Most in
mid-shelf waters.
Pelagic
Most in 18-22ºC.
Larvae
Most 30-70 m depths, May-Sept, peak in
July.
Strongly
associated with
the surface.
18-26ºC in Mid-Atlantic
Bight
Juveniles
Mostly estuarine areas and river mouths,
including Narragansett Bay. Also coast
beaches and surf zones.
Mostly sand,
particularly
along coast, but
some mud, silt,
clay. Also uses
vegetation beds.
In most studies, arrive >
20ºC, remain in
temperatures up to 30ºC,
emigrate when declines to
15ºC. Can not survive
below 10ºC or above 34ºC.
Fall migration in 18-22ºC
on inner continental shelf.
Adults
Generally oceanic, nearshore to well
offshore over continental shelf. Not
Pelagic
Warm water, usually > 14-
16ºC.
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uncommon in bays, larger estuaries, as
well as coastal waters.
510.2.9. Butterfish (Poronotus triacanthus)
1. Butterfish are found from Newfoundland to Florida. In the Ocean SAMP area, butterfish
are targeted by commercial fishermen.
Life History
2. Butterfish are pelagic fishes, forming loose schools (NEFSC 1999b). Butterfish are found
in Narragansett Bay and in Rhode Island and Block Island Sounds from late spring
through fall, appearing off Rhode Island in late April. They spawn usually within a few
miles of the coast during the late spring and early summer, and migrate to the edge of the
continental shelf during the winter (Collette and Klein-MacPhee 2002). Butterfish eggs
are found within Narragansett Bay from June through August (NEFSC 1999b). The eggs
of the butterfish are buoyant, and will hatch within two days in waters of around 65
degrees Fahrenheit (18 degrees Celsius). The juveniles will grow to about half their adult
size within their first year (Collette and Klein-MacPhee 2002). Juvenile butterfish may
associate with jellyfish during the summer to avoid predators (NEFSC 2006a). Butterfish
mature in their second summer (Collette and Klein-MacPhee 2002). They can reach up to
twelve inches (30 cm) in length, although most harvestable butterfish are between six and
nine inches (15 and 23 cm). The maximum reported age for butterfish is six years,
although most probably only live two to three years (Collette and Klein-MacPhee 2002).
Habitat
3. Butterfish feed primarily on tunicates and mollusks, as well as cnidarians, polychaetes,
crustaceans, and other invertebrates (Collette and Klein-MacPhee 2002). Ctenophores
have been found to make up an important component of the diet of juvenile butterfish in
Narragansett Bay (Oviatt and Kremer 1977). They will often come close to shore into
sheltered bays and estuaries, and they have a preference for sandy bottom as opposed to
rocky or muddy bottom. They spend much of their time near the surface when they are
near to shore, but spend the winter and early spring near the bottom at depths of up to
100-115 fathoms (183 to 210 m) (Collette and Klein-MacPhee 2002). Butterfish serve as
prey to a number of species including hake, bluefish, weakfish, and swordfish, and are
used commonly as bait in recreational tuna fisheries (Ross 1991).
Fishery
4. The butterfish stock is currently managed by the Mid-Atlantic Fishery Management
Council under the Atlantic Mackerel, Squid, and Butterfish Fishery Management Plan.
There is considerable uncertainty in butterfish abundance estimates. Discards of
butterfish in fisheries targeting other species, particularly in the squid fishery, is an
important source of mortality (NEFSC 2006a).
Table 5.11. Habitat characteristics of butterfish. (NEFSC 1999b)
Life Stage
Habitat
Substrate
Temperature
Eggs
Surface waters from continental shelf into
estuaries and bays; collected to about 60 m
deep in shelf waters.
Pelagic
Most eggs
collected between
11-17ºC.
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Larvae
Surface waters from continental shelf into
estuaries and bays; collected to about 60 m
deep in shelf waters; common in high salinity
zone of estuaries and bays; may spend day
deeper in the water column and migrate to the
surface at night.
Pelagic
4.4-27.9ºC
Juveniles
From surface waters to depth on continental
shelf; into coastal bays and estuaries;
common in inshore areas, including the surf
zone, and in high salinity and mixed salinity
zones of bays and estuaries. Most collected in
< 120 m. Commonly occur in bays and
estuaries from MA to VA from spring
through fall.
Larger individuals
found over sandy
and muddy
substrates.
4.4-29.7ºC
Adults
From near surface waters in summer to depths
of 270-420 m on continental shelf in winter;
into coastal bays and estuaries; common in
inshore areas, including the surf zone, and in
high salinity and mixed salinity zones of bays
and estuaries. Most collected in < 180 m.
Spawning occurs on continental shelf, inshore
areas, and in bays and estuaries.
Schools found
over sandy,
sandy-silt, and
muddy substrates.
4.4-26.0ºC;
Spawning does
not occur at <
15ºC.
510.2.10. False Albacore (Euthynnus alletteratus)
1. The false albacore is also referred to as the little tunny. These fish are found in the
tropical and temperate waters of the Western Atlantic from New England south to Brazil.
Unlike other tunas, the false albacore is mostly scaleless (Ross 1991). In the Ocean
SAMP area, false albacore are one of the most prized fish pursued by recreational
fishermen for catch and release.
Life History
2. False albacore are usually about 25 inches (63 cm) in length, although they can grow to
40 inches (101 cm). They reach sexual maturity at about 15 inches (38 cm). The fish
spawn from April to November (NMFS 2007b). A female will produce as many as 1.8
million eggs, which are released in several large batches during the spawning season.
They are usually found traveling in large schools with similar-sized individuals, and
sometimes in mixed schools with Atlantic bonito (Ross 1991).
Habitat
3. The false albacore is usually found near the coast, or around offshore shoals or islands
further out on the continental shelf. In the Atlantic, the false albacore is rarely found in
waters beyond the continental shelf. The fish prefers areas with strong currents. False
albacore migrate northward along the Atlantic coast of the United States in spring and
summer, moving from the North and South Carolina coasts in May and June to southern
New England by August and September. The false albacore feeds during the daytime on
schools of sand lance, herring, mackerel, and young false albacore, as well as squid,
euphausiid shrimp, and other crustaceans. They are preyed upon by yellowfin tuna and
various species of sharks (Ross 1991).
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Fishery
4. False albacore are managed internationally through the International Commission for the
Conservation of Atlantic Tunas. At present, there is no Fishery Management Plan in
place for false albacore; recreational anglers are not required to have a permit to fish for
this species. There are no size or bag limits for false albacore.
Table 5.12. Habitat characteristics of false albacore. (Ross 1991)
Life Stage
Habitat
Substrate
Temperature
Juveniles/Adults Near-coastal waters or around
offshore shoals or islands. Usually
on continental shelf, in areas with
strong currents
Pelagic
N/A
510.2.11. Goosefish (monkfish) (Lophius americanus)
1. The goosefish, also commonly called monkfish, is found from Newfoundland to North
Carolina, and in the Gulf of Mexico. In the Ocean SAMP area, monkfish are targeted by
commercial fishermen.
Life History
2. Male monkfish become sexually mature at age four, and females at age five. They
reproduce in shallow water from spring through early fall; typically from late June
through mid-September in New England. They produce large masses of eggs in a single
ribbon that can be up to 25-36 feet (7-11 m) in length that float within the water column,
and can produce up to 2.8 million eggs at one time. By the time the fry reach about two
inches (5 cm) in length, they become bottom-dwellers. They can reach four feet (1.2 m)
in length and weigh up to 50 pounds (23 kg) (Ross 1991).
Habitat
3. Monkfish are found from the tideline out to depths of greater than 2,000 feet (610 m) on
the continental slope. They live on various types of substrate, including sand, gravel,
rocks, mud, and beds of broken shells. They have been found in a variety of
temperatures, from 32 degrees to 70 degrees Fahrenheit (0 to 21 degrees Celsius), but
prefer temperatures of 37-48 degrees Fahrenheit (3 to 9 degrees Celsius). Young
monkfish fry will feed on copepods, crustacean larvae, and arrow worms (Ross 1991).
Adult monkfish are voracious predators, feeding on skates, herring, mackerel, and silver
hake, as well as lobsters and crabs. The most important prey species for monkfish in
southern New England are little skate, red hake, sand lance, and other monkfish (Collette
and Klein-MacPhee 2002). The monkfish often feeds by lying motionless in eelgrass,
waving its “lure” to attract fish and then opening its enormous mouth to suck in the fish,
earning it the nickname “angler”. The monkfish also eats seabirds, including cormorants,
herring gulls, loons, and other sea birds, the practice of which has given the fish the
nickname “goosefish”, although there have been no documented cases of a monkfish
eating a goose. A monkfish can have up to half its own bodyweight in its stomach (Ross
1991), and can swallow a fish almost its own size (Collette and Klein-MacPhee 2002).
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Fishery
4. Monkfish are currently managed under the Monkfish Fishery Management Plan by the
New England and Mid-Atlantic Fishery Management Councils. Management measures
include limited access, days-at-sea limitations, mesh size restrictions, minimum size
limits, and trip limits. Monkfish are managed as two separate stocks; the monkfish in
Rhode Island waters are considered part of the southern stock, which extends from the
southern portions of Georges Bank to the Mid-Atlantic. Based on the 2007 stock
assessment, monkfish biomass is 29% above that necessary to support maximum
sustainable yield, and so monkfish are not considered overfished, nor is overfishing
occurring (NMFS 2010b). Monkfish are caught throughout the Ocean SAMP area.
Table 5.13. Habitat characteristics of goosefish (monkfish). (NEFSC 1999c)
Life Stage
Habitat
Substrate
Temperature
Eggs
Upper water column, inner to mid-continental
shelf, southern New England, and Mid-Atlantic
Bight; not in estuaries. Contained in long mucus
veils that float near or at surface.
Pelagic
4-18°C or higher
Larvae
Mainly mid-shelf in southern New England and
Mid-Atlantic Bight. Upper to lower water column,
at depths of 15 to > 1000 m; mostly 30-90 m.
Pelagic
6-20°C, most in
11-15°C
Juveniles
Southern New England: mostly mid to outer shelf.
Seabed, > 20 m, peak abundance at 40-75 m.
Mud to gravelly sand,
algae, and rocks.
2-24°C, most 3-
13°C
Adults
Southern New England/Mid-Atlantic Bight:
inshore in winter, offshore in summer fall.
Seabed, 1- 800 m, most 50-99 m, sometimes at
surface.
Mud to gravelly sand,
algae, and rocks. Will
hide in eelgrass to
ambush prey.
Seasonally
variable, 0-24°C;
mostly 4-14°C.
510.2.12. Longfin Squid (Loligo pealeii)
1. Longfin squid are distributed from Cape Cod through Cape Hatteras. In the Ocean SAMP
area, longfin squid are pursued by commercial fishermen.
Life History
2. The longfin squid grows to about eight to twelve inches long (20 to 30 cm), and is
sexually dimorphic, with males growing faster than females. It moves by means of jet
propulsion, taking in water through a siphon and then expelling it. The life span of the
longfin squid is thought to be about six months (Macy and Brodziak 2001). Adult longfin
squid are demersal during the day, coming to the surface at night to feed. Newly hatched
squid are found at the surface, and move deeper in the water column as they grow,
becoming demersal when they reach just under two inches (45 mm) in length (NEFSC
2005b). There is evidence that squid spawn throughout the year, with two main spawning
periods in the summer and winter (Macy and Brodziak 2001).
Habitat
3. The greatest abundance of longfin squid are found in continental shelf and slope waters
at depths between 55 and 92 fathoms (100 and 168 m). They generally migrate inshore to
waters off Rhode Island and elsewhere in May or June, and by late November/early
December they migrate to deeper waters along the edge of the continental shelf (Macy
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and Brodziak 2001). The adults feed on small fish, while juveniles feed on small
crustaceans (Rathjen 1973). Squid are an important prey species to a number of other
species including sharks, haddock, hakes, striped bass, black sea bass, bluefish, scup,
mackerel, summer flounder, and tunas (Ross 1991).
Fishery
4. Two separate fisheries exist for longfin squid; an inshore fishery in summer and fall, and
a larger offshore commercial fishery during the winter months, when the squid migrate to
the edge of the continental shelf (Macy and Brodziak 2001). The longfin squid stock is
currently managed by the Mid-Atlantic Fishery Management Council under the Atlantic
Mackerel, Squid, and Butterfish Fishery Management Plan. They are managed through
the use of permits, quotas, and gear restrictions. Landings of longfin squid have declined,
due in part to seasonal closures (NEFSC 2006a). The relative biomass measures of
longfin squid were below average through 2005, but increased to slightly above average
in 2007. Estimates of the level of biomass needed to support maximum sustainable yield
for longfin squid are not currently available. Overfishing is not presently occurring on
this species (NMFS 2010b).
Table 5.14. Habitat characteristics of longfin (loligo) squid. (NEFSC 2005b)
Life Stage
Habitat
Substrate
Temperature
Eggs
Shallow waters, <50m and near shore.
Egg masses are
Commonly
found on
sandy/mud
bottom; usually
attached to
rocks/boulders,
pilings, or
algae.
Eggs found in waters
10-23ºC; usually > 8ºC.
Optimal development at
12ºC.
Larvae
Found in coastal, surface waters in
spring, summer, and fall. Hatchlings
found in surface waters day and night.
Move deeper in water column as they
grow larger.
Pelagic
Found at 10-26ºC (at
lower temperatures
found at higher
salinities).
Juveniles
Inhabit upper 10 m at depths of 50-100 m
on continental shelf. Found in coastal
inshore waters in spring/fall, offshore in
winter. Migrate to surface at night.
Pelagic
Found at 10-26ºC.
Juveniles prefer warmer
bottom temperatures
and shallower depths in
fall than adults.
Adults
March-October: inshore, shallow waters
up to 180 m. Winter: offshore deeper
waters, up to 400 m on shelf edge. Most
abundant at bottom during the day; move
upwards at night. Generally found at
greater depths and cooler bottom
temperatures in the fall than juveniles.
Mud or sandy
mud
Found at surface
temperatures ranging
from 9-21ºC and bottom
temperatures ranging
from 8-16ºC.
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510.2.13. Menhaden (Brevoortia tyrannus)
1. Atlantic menhaden (Brevoortia tyrannus), also called pogies, bunkers, and fatbacks, are
found in estuarine and coastal waters stretching from Nova Scotia to northern Florida.
Menhaden are a prey species that provide food to many commercially and recreationally
important species. In addition, menhaden are used as bait in the lobster fishery.
Life History
2. Adult and juvenile menhaden form large schools near the surface, mostly in estuaries and
along the shore from early spring through early winter. During the summer, menhaden
schools will stratify by age and size along the coast; older, larger menhaden are generally
found further north. In the fall and early winter, menhaden of all ages and sizes will
migrate south to spawn in the waters between New Jersey and North Carolina, usually
about twenty to thirty miles offshore. The eggs that are released float offshore; when the
juveniles hatch, they will be carried into estuarine nursery areas by ocean currents where
they will spend the first year of their lives, migrating south in the winter (ASMFC
2008a). Adults average about 7- 12 inches (20-30 cm) in length and weigh 0.5 – 1.3
pounds (0.25-0.6 kg) (Collette and Klein-MacPhee 2002).
Habitat
3. Menhaden spawn offshore in the waters between New Jersey and North Carolina during
the fall and early winter, and spend the rest of the year in estuaries, migrating further
north. Menhaden feed on plankton, most commonly diatoms and small crustaceans, by
straining it from the water using their gill rakers. They themselves serve as an important
food source for many larger fish, including striped bass and bluefish (ASMFC 2008a).
This is highlighted by the 2006 menhaden stock assessment, which found that predation
mortality is most likely the highest cause of natural mortality (Atlantic Menhaden
Technical Committee 2006).
Management
4. Menhaden are managed by the Atlantic States Marine Fisheries Commission, and are
managed through the use of seasonal restrictions and management areas in Rhode Island.
Commercial fishing for menhaden typically includes both a bait fishery and a reduction
fishery, where the fish are processed into fishmeal and oil. Rhode Island does not allow a
reduction fishery to occur in state waters, but there is a bait fishery taking place here.
They are of commercial importance largely because of their use as bait for the lobster
fishery, though they are also used by recreational fishermen as bait in the striped bass and
bluefish fisheries. Although they are typically fished from Narragansett Bay rather than
from the Ocean SAMP area, menhaden pass through the Ocean SAMP area. However,
due to current restrictions placed on the bait fishery in Narragansett Bay, fishing pressure
may transfer in to the Ocean SAMP area in the future. Menhaden were historically a
major fishery in Rhode Island (see Section 530). Some have argued that local stocks have
been depleted due to fishing pressure off mid-Atlantic states, which has prevented
menhaden from migrating northward (Oviatt et al. 2003). According to the Atlantic
States Marine Fisheries Commission, menhaden are not overfished, and overfishing is
not occurring (ASMFC 2008a).
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Table 5.15. Habitat characteristics of menhaden (ASMFC 2008a; Collette and Klein-MacPhee 2002).
Life Stage
Habitat
Substrate
Temperature
Eggs
Buoyant; hatch at sea.
Pelagic
N/A
Larvae
Estuarine nursery areas with salinity
< 10 ppt.
N/A
N/A
Juveniles
Live in estuaries for first year of life.
Unconsolidated
bottom with sand,
mud, organic
material; rocky
coves with
cobble, rock, and
sand bottoms in
northern part of
range.
N/A
Adults
Nearshore and inland tidal waters.
Ranges from a
bottom
composition of
sand, mud and
organic material
to marine sand
and mud with
increasing
amounts of rocks
in the more
northerly areas.
Prefer water temperatures
near 18° C.
510.2.14. Scup (Stenotomus chrysops)
1. Scup, also known as porgy, are a migratory species found from Cape Cod to Cape
Hatteras. Scup are pursued by both recreational and commercial fishermen in the Ocean
SAMP area.
Life History
2. Scup spawn in inshore waters during the summer, with spawning reaching its peak in
June off southern New England. The eggs will hatch about 40 hours after fertilization.
Larval scup are pelagic and are found in coastal waters during the warmer months. Scup
become sexually mature at age two or three (ASMFC 2008a). They form into schools of
similarly-sized individuals. They can grow up to six pounds, but rarely exceed two
pounds (one kg) in weight and fourteen inches (36 cm) in length. They can reach fifteen
years of age, although it appears this is rare because of high mortality rates due to
predation and fishing (Ross 1991).
Habitat
3. Scup are most commonly found in waters between 55 and 77 degrees Fahrenheit (13 and
25 degrees Celsius). They spend the winters in offshore waters from southern New Jersey
to Cape Hatteras, and spawn in the summer in inshore waters from southern New
England to Long Island, moving to New England waters in May until leaving in October.
Juvenile scup inhabit coastal habitats, and will sometimes dominate the fish population
of estuarine areas during the summer months (ASMFC 2008a). They prefer areas with
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smooth or rocky bottoms, and are often found around piers, rocks, offshore ledges,
jetties, and mussel beds. During the winter, they prefer depths of 240 to 600 feet (73 to
183 m), where the water temperature is at least 45 degrees Fahrenheit (7 degrees
Celsius). Adult scup feed on bottom invertebrates, including small crabs, squid, worms,
clams, mussels, amphipods, jellyfish, and others. They are eaten by a variety of different
fishes; as many as 80% of all juvenile scup annually are eaten by fish such as cod,
bluefish, striped bass, and weakfish (Ross 1991).
Fishery
4. Scup is important as both a recreational and commercial species. Rhode Island has the
largest share of scup landings in state waters along with New Jersey. The species is
jointly managed by the Mid-Atlantic Fishery Management Council and the Atlantic
States Marine Fisheries Commission through the Summer Flounder, Scup, and Black Sea
Bass Fishery Management Plan (ASMFC 2008a). Scup spawning stock biomass had
declined greatly in the mid-1990s, but has steadily increased since then. Overfishing is
not occurring, and the stock is not overfished. Scup biomass for 2008 was estimated to be
104% above that required for maximum sustainable yield. Spawning stock biomass was
estimated to be around 188,000 metric tons in 2008 (NMFS 2010b).
Table 5.16. Habitat characteristics of scup. (NEFSC 1999d)
Life Stage
Habitat
Substrate
Temperature
Eggs
Water column, < 30 m in depth,
Coastal Virginia – Southern New
England.
Buoyant in water
column.
11-23°C; most
common 12-14°C
Larvae
Water column, < 20 m until juvenile
transition.
Water column
14-22°C; peak
densities at 15-
20°C
Juveniles
Young-of-year: Estuarine and coastal;
from intertidal to about 38 m. Winter
juveniles: Mostly > 38 m depth; mid
and outer continental shelf; sometime
in deep estuaries.
Sand, mud, mussel,
and eel grass beds.
Greater than ~9-
27°C; mostly 16-
22°C
Adults
2-38 m in summer. Mostly 38-185 m
depths; mid/outer continental shelf in
winter.
Fine to silty sand,
mud, mussel beds,
rock, artificial reefs,
wrecks, and other
structures in summer.
Weedy and sandy
habitats when
spawning.
~7-25°C
510.2.15. Shark, Blue (Prionace glauca)
1. Sharks are pursued by recreational fishermen in the Ocean SAMP area. Whereas a
number of different shark species may be pursued by fishermen, the most commonly
targeted ones are blue, shortfin mako, and thresher. Compared with other marine fishes,
sharks have a very low reproduction potential because of a combination of factors
including slow growth, late sexual maturity, infrequent reproductive cycles, a small
number of young produced, and requirements for nursery areas. These factors make
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sharks highly vulnerable to overfishing (ASMFC 2008a). The blue shark is widely
distributed in both inshore and offshore areas throughout the North Atlantic, and is one of
the most commonly encountered shark species.
Life History
2. Male blue sharks grow to between five and six feet long at maturity. Like other shark
species, the eggs are fertilized internally. Females will often not give birth until up to two
years after mating, storing the sperm for up to a year after the first time they mate, and
then incubating the embryo for up to one year. The young are between fourteen and
eighteen inches (46 cm) at birth. Females may bear up to 82 young, although the average
number is much lower. The largest blue sharks measure eleven or twelve feet (more than
3.5 m) in length (Ross 1991).
Habitat
3. Blue sharks are found in the Northwest Atlantic from May through October, often in
waters of depths between 100 and 130 feet (30 and 40 m) off southern New England.
Large females will typically migrate northward and inshore during the spring, and
smaller females and males will follow later in the year. During the fall, blue sharks will
migrate southward along the continental shelf to the margins of the Gulf Stream. They
appear to prefer temperatures between 55 and 64 degrees Fahrenheit (13 and 18 degrees
Celsius). They are often found near the surface in temperate areas, but frequent deeper,
cooler waters in tropical regions. Blue sharks feed on squid and octopus, as well as
bluefish, red and silver hakes, mackerel, menhaden, and herring (Ross 1991).
Table 5.17. Habitat characteristics of blue shark. (Ross 1991)
Life Stage
Habitat
Substrate
Temperature
Juveniles/Adults Often found in waters of 30 to 40
meters of depth off southern New
England coastline.
Pelagic
From 8 to 27ºC, prefer
waters from 13 to 18ºC
Shark Fishery
4. Fishing efforts for most shark species are controlled by means of possession limits.
Sharks are managed jointly by NMFS, through the Consolidated Atlantic Highly
Migratory Species Fishery Management Plan (NMFS 2006), and by the Atlantic States
Marine Fisheries Commission, under the Interstate Fishery Management Plan for
Atlantic Coastal Sharks (ASMFC 2008d). The Atlantic States Marine Fisheries
Commission’s plan complements federal shark management actions and places special
attention on the protection of pregnant females and juveniles in inshore nursery areas.
510.2.16. Shark, Shortfin Mako (Isurus oxyrinchus)
1. Mako sharks are one of the three shark species most commonly targeted by recreational
fishermen in the Ocean SAMP area.
Life History
2. Mako sharks spend the summer months at northern latitudes, and migrate south along the
continental shelf to winter in the Caribbean during the winter. Males are sexually mature
at three to four years of age, and females at seven years of age. Like other sharks,
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fertilization of egg cells occurs internally within mako sharks. After one year of
embryonic development, the female mako shark will give birth to from one to several
young, each measuring more than two feet long at birth. Internal incubation allows newly
born sharks to be more highly developed than species hatched through external
fertilization, and provides them with a higher probability of survival than for larval fish
(Ross 1991). Most adult mako sharks are between five and eight feet (1.5 to 2.5 m) in
length.
Habitat
3. The mako shark is a pelagic shark not found in waters less than thirty feet (9 m) deep.
They are usually found offshore either at or near the surface (Ross 1991). Mako sharks
prefer tropical and warm temperate waters; southern New England is the northern part of
their range. In southern New England waters, bluefish may make up to 80% of a mako
shark’s diet. Mako sharks also eat small schooling fish such as mackerel and herring,
squid, and larger species including swordfish, bonito, and tuna species (Ross 1991). The
current status of the shortfin mako shark is uncertain, but it may be approaching an
overfished condition (NMFS 2010b).
Table 5.18. Habitat characteristics of mako shark. (Ross 1991)
Life Stage
Habitat
Substrate
Temperature
Juveniles/Adults Oceanic, never within waters less
than 9 m deep. Found at or near the
surface.
Pelagic
N/A
4. Fishing efforts for most shark species are controlled by means of possession limits. Mako
sharks are managed by NMFS, under the Consolidated Atlantic Highly Migratory
Species Fishery Management Plan (NMFS 2006), and by the Atlantic States Marine
Fisheries Commission under the Interstate Fishery Management Plan for Atlantic Coastal
Sharks (ASMFC 2008d). There is a great deal of uncertainty over stock levels of mako
sharks in the North Atlantic; the current stock levels may be below the biomass required
to support maximum sustainable yield, suggesting the stock may be approaching an
overfished condition (NMFS 2010b).
510.2.17. Shark, Thresher (Alopias vulpinus)
1. Thresher sharks are sometimes targeted by recreational fishermen in the Ocean SAMP
area.
Life History
2. Thresher sharks are ovoviviparous; they develop in utero without a placental attachment.
Females usually give birth to two to four pups at a time, and they are typically longer
than 150 cm (59 inches) at birth. It is thought thresher sharks reproduce annually, as most
mature female sharks caught are pregnant. Thresher sharks may attain a length of up to
300 cm (118 inches) (Collette and Klein-MacPhee 2002). It is estimated they may live
anywhere from 19 to 50 years (NMFS 2010b).
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Habitat
3. Thresher sharks are an epipelagic species, found in both coastal and oceanic waters. They
are found from Nova Scotia to Argentina, and are common off southern New England
during the summer months. Juveniles are more likely to be found in inshore waters, and
may also be found in coastal bays. Adults are often found over the continental shelf
(Collette and Klein-MacPhee 2002). They are most common in temperate waters, but can
also be found in cold-temperate and tropical waters (NMFS 2010b). Most young sharks
are seen in southeast U.S. waters, so it has been suggested that the sharks may have a
pupping ground in the south, but it is not known whether this is the case. Thresher sharks
use their long caudal fins to stun their prey. They feed primarily on small schooling
fishes including herring, menhaden, bluefish, sand lance, and mackerel, as well as on
bonito and squids. Thresher sharks will often feed in groups, herding schools of fish into
a tight group, and then whipping them with their tails (Collette and Klein-MacPhee
2002).
Table 5.19. Habitat characteristics for thresher shark. (Collette and Klein-MacPhee 2002)
Life Stage
Habitat
Substrate
Temperature
Juveniles
Inshore waters, coastal bays.
Pelagic
N/A
Adults
Oceanic; over the continental shelf.
Pelagic
N/A
Fishery
4. The status of Atlantic thresher sharks is unknown; it is not known if they are overfished
or if overfishing is occurring. They are often caught as by-catch in longline fisheries
targeting tuna and swordfish, and are taken recreationally in rod and reel fisheries
(NMFS 2010b). Atlantic thresher sharks are managed by NMFS, under the Consolidated
Atlantic Highly Migratory Species Fishery Management Plan (NMFS 2006), and by the
Atlantic States Marine Fisheries Commission under the Interstate Fishery Management
Plan for Atlantic Coastal Sharks (ASMFC 2008d).
510.2.18. Silver Hake (Merluccius bilinearis)
1. Silver hake, or whiting, are found along the continental shelf of North America, from
Canada to the Bahamas, and are most abundant between Newfoundland and South
Carolina (Collette and Klein-MacPhee 2002). There are two stocks of silver hake; one in
the Gulf of Maine and northern Georges Bank, and the other on southern Georges Bank
and the Mid-Atlantic Bight. In the Ocean SAMP area, silver hake are targeted by
commercial fishermen.
Life History
2. Silver hake can reach a length of two and a half feet (76 cm) and weigh up to five pounds
(2.3 kg), but usually are only around fourteen inches in length (36 cm). They do not form
definitive schools, but will swim together in groups (Collette and Klein-MacPhee 2002).
Silver hake spawn throughout the year, peaking from May through November, and with a
peak in May to June in the southern stock (NEFSC 2004c). They reach sexual maturity at
two to three years of age. The eggs are pelagic, and hatch within two days (Ross 1991).
The larvae are just one-tenth of an inch (2.8 mm) in length after hatching. During their
first summer or fall, when they are still less than an inch (17-22 mm), the silver hake
larvae will descend to the bottom as juveniles (NEFSC 2004c). Females live longer and
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grow faster than males; males usually don’t live past six years, while females may
occasionally live to between twelve and fifteen years in age (Ross 1991).
Habitat
3. Silver hake are wanderers, unconcerned with the depth or with the sea floor. They are
sometimes found near the bottom, and sometimes close to the surface, as they chase prey
throughout the water column. They are found as deep as 2400 feet (122 m) as well as just
below the tide line. When they are found near the bottom, they are usually on sandy or
pebbly ground, or mud (Collette and Klein-MacPhee 2002). There are two major stocks
of silver hake, one north and one south of Georges Bank. The stock of silver hake found
off Rhode Island spend their winters along the continental slope south of Georges Bank,
and migrate to shallower waters in southern New England for the spring and summer.
They spawn on the southern slopes of Georges Bank and Nantucket Shoals, and south of
Martha’s Vineyard (Ross 1991). The area between Cape Cod and Montauk Point, which
includes the Ocean SAMP area, is a primary spawning ground for silver hake (NEFSC
2004c). Silver hake will move south and to offshore waters during the winter (NEFSC
2004c). Voracious predators, silver hake prey on many different schooling fish including
herring, young mackerel, sand lance, and smaller silver hake (Collette and Klein-
MacPhee 2002). They themselves are food for cod, mackerel, swordfish, spiny dogfish,
flounders, and larger silver hake (Ross 1991).
Fishery
4. Silver hake and red hake were the two primary species targeted by Rhode Island’s
industrial fishery in the 1950s (Olsen and Stevenson 1975). Silver hake are managed by
the New England Fishery Management Council as part of the “small mesh multispecies”
management unit of the Northeast Multispecies Fishery Management Plan. The southern
stock of silver hake is not currently considered to be overfished, nor is overfishing
occurring, but there are concerns about the age structure of the stock; specifically that
there are very few fish over the age of four within the population. Significant numbers of
juvenile silver hake are discarded in otter trawl fisheries, which may limit opportunities
to rebuild this stock (NEFSC 2006a).
Table 5.20. Habitat characteristics of silver hake. (NEFSC 2004c)
Life Stage
Habitat
Substrate
Temperature
Eggs
Most abundant in deep parts of Georges Bank
and bank off southern New England; in
southern New England waters July-October;
most from 50-150 m.
N/A
Peak abundance from
11-17ºC.
Larvae
Present in Block Island Sound in June
through November; abundant in southern
New England July-September; most at depths
from 50-130 m.
N/A
Temperature preference
varies based on annual
warming and cooling
cycle.
Juveniles
Migrate to deeper waters of the continental
shelf as water temperatures decline in the
autumn and return to shallow waters in spring
and summer. Large concentrations south of
RI in fall.
Prefer mud
bottoms, also
transitional
and sand
bottoms.
Wide temperature
ranges.
Adults
Migrate to deeper waters of the continental
shelf as water temperatures decline in the
Prefer mud
bottoms, also
Prefer temperatures
greater than 9ºC in
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autumn and return to shallow waters in spring
and summer to spawn. Frequent spawning in
October south of Martha’s Vineyard. Older
hake prefer the warmer waters of the shelf
slope and deep-water shelf area. Found as
deep as 122 m as well as in shallow waters.
transitional
and sand
bottoms.
Southern New England.
Found at wide
temperature ranges.
Spawning peaks
between 7 and 13ºC.
510.2.19. Skates
1. Common skates to Rhode Island waters targeted in commercial fisheries are the little
skate (Leucoraja erinacea), also known as the summer or common skate, and the winter
skate (Leucoraja ocellata), also called the big skate. The two species are very similar in
appearance, and difficult for many people to tell apart. Skates are listed and discussed
here together as this is how most skate fishery landings are reported to NMFS (NMFS
2009a).
Life History
2. Winter skates mature at a length of 24 inches (61 cm), and little skates at a length of
sixteen inches (41 cm). The eggs are fertilized inside the female’s reproductive tract, and
then released into the water where much of the embryo’s development will take place. It
is believed the winter skate spawns in southern New England waters in summer and fall.
The little skate spawns throughout the year, with spawning activity in southern New
England peaking in June and July. Female skates produce egg cases two at a time, and
may produce between 60 and 150 per year. The young hatch between six and nine
months after fertilization, and are about three and a half inches (9 cm) long once hatched.
The little skate will grow to about 21 inches (53 cm), and the winter skate to 42 inches
(107 cm) (Ross 1991).
Habitat
3. Skates are most abundant from shallow waters to depths of up to 360 feet (110 m). The
winter skate prefers temperatures between 34 to 70 degrees Fahrenheit (1 and 21 degrees
Celsius), and little skates between 34 to 66 degrees Fahrenheit (1 and 19 degrees
Celsius). The little skate is distributed along the coast from Chesapeake Bay to Georges
Bank in winter and spring, with large numbers along the Long Island coast. They are
most abundant between Georges Bank and Long Island in summer and fall. The winter
skate is concentrated on Georges Bank throughout the year, and along the eastern shore
of Long Island in the winter and spring. Both species of skate feed largely on rock crabs,
shrimp, and squid, but also frequently eat amphipods, polychaetes, razor clams, and
small fishes. In one study in Block Island Sound, skates fed almost exclusively on digger
amphipods. Skates are commonly eaten by monkfish (Ross 1991).
Fishery
4. A market for skate as bait developed in southern New England in the 1980s, and landings
have increased substantially. Prior to this, skate was mostly taken as bycatch or targeted
as an industrial fish. The little skate is the species primarily targeted in the bait fishery,
whereas the winter skate is sometimes also targeted as food fish for its wings, which are
sold in a growing export market. Skates are frequently taken as bycatch in groundfishing
operations. Skates are federally managed as a group under the Skate Fishery
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Management Plan through the New England Fishery Management Council. Little skate is
not currently overfished, nor is overfishing occurring. Winter skate is not considered to
be overfished at present, but overfishing is occurring for this species (NEFSC 2006a).
Table 5.21. Habitat characteristics of little skate. (NEFSC 2003a)
Life Stage
Habitat
Substrate
Temperature
Eggs
Egg capsule is deposited on the
bottom, perhaps in water < 27 m
deep.
May be partially buried in
sand.
Embryonic growth
takes place when
temperatures are > 7-
8ºC and increases
with increasing
temperature.
Juveniles/Adults Generally move into shallow
water during spring, deeper
water in winter. May leave some
estuaries for deeper water during
warmer months. Generally
caught at depths <111 m, but
occasionally at depths > 183 m.
Sandy or gravelly
bottoms, but also on mud.
Southern New England at
55 m. Skates are known to
remain buried in
depressions during the day
and are more active at
night.
Overall temperature
range is 1-21ºC,
although most are
found between 2-
15ºC.
Table 5.22. Habitat characteristics of winter skate. (NEFSC 2003b)
Life Stage
Habitat
Substrate
Temperature
Juveniles/Adults Generally caught at depths from
shoreline to 371 m, although
most abundant <111 m.
Prefer sand and gravel
bottoms.
Recorded over a
temperature range of
-1.2ºC to 19ºC.
510.2.20. Spiny Dogfish (Squalus acanthias)
1. The spiny dogfish (Squalus acanthias) is a coastal shark, and is the most abundant shark
in the Northwest Atlantic, ranging from Labrador to Florida.
Life History and Habitat
2. Spiny dogfish have a long life, low fecundity, late maturation, and a long gestation
period, making it highly vulnerable to population collapse. Spiny dogfish are born in the
fall or winter, and are about 26-27 cm (10 inches) in length at birth. They do not reach
maturity for ten or more years. Mating occurs in the winter months, and pups are
delivered on the offshore wintering grounds (ASMFC 2008a). Females will produce a
litter of between 1-15 pups, usually averaging 6-7 pups, and give birth every two years.
Habitat
3. Spiny dogfish are an important predator in the Ocean SAMP area, and eat fish of many
sizes, including herring and hakes, squid, and ctenophores. They also eat bivalves,
especially scallops, off southern New England. Dogfish diets have changed in response to
changes in abundance of certain fish species due to fishing pressures. They migrate north
during the spring and summer, and south in the fall and winter. Juvenile and adult spiny
dogfish are abundant in the Mid-Atlantic waters extending to the southern part of
Georges Bank in winter. During the summer months, they are found farther north in
Canadian waters, and will move inshore into bays and estuaries (ASMFC 2008a). In the
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fall they are commonly found closer to shore, and are abundant off Martha’s Vineyard
and Nantucket (NEFSC 2006a).
Management
4. The spiny dogfish is managed jointly by the Mid-Atlantic and New England Fishery
Management Councils and the Atlantic States Marine Fisheries Commission. The fishery
is managed primarily through trip limits and seasonal closures. Some Rhode Island
fishermen participate in the spiny dogfish harvest, and they are commonly found within
the Ocean SAMP area. Dogfish are frequently taken as bycatch with otter trawls and
other gear targeting groundfish, and were heavily targeted by foreign fleets before the
enactment of the EEZ. Management measures have been highly effective in reducing
landings and bycatch mortality, and the stock is not currently considered overfished, nor
is overfishing occurring. The biomass of spiny dogfish exceeded target levels in 2008
and was considered rebuilt; in 2009 biomass was estimated to be 163,256 metric tons
(Rago and Sosebee 2010). In 2010, there was a proposal to list spiny dogfish in
Appendix II of the Convention on the International Trade in Endangered Species, though
this proposal was rejected (CITES 2010).
Table 5.23. Habitat characteristics of spiny dogfish. (NMFS 2010b; ASMFC 2008a)
Life Stage
Habitat
Substrate
Temperature
Juveniles
Most at depths below 50m.
Pelagic
7-15°C
Adults
Inshore in bays and estuaries in
summer; offshore in winter. Large
females may prefer nearshore shelf
and lower salinities. Found at depths
from 1-500 m.
Pelagic; demersal
at times, found
over soft sediment
such as mud,
sand, and silt
where food is
available.
7-15°C
510.2.21. Striped Bass (Morone saxatilis)
1. Atlantic striped bass range from the St. Lawrence River in Canada south to the St. John’s
River in Florida. They are an anadromous species, spending their life in estuaries and in
the ocean. They are sometimes referred to as the striper or rockfish. Striped bass are
usually found in Rhode Island waters from April through November. In the Ocean
SAMP area, striped bass are one of the most important and popular fish pursued by
recreational fishermen, and are also targeted in commercial fisheries.
Life History
2. Striped bass can live at least thirty years. They may grow up to 150 cm (59 inches) in
length, and between 55 and 77 pounds (25 to 35 kg) (Collette and Klein-MacPhee 2002),
although the largest striped bass ever caught weighed 125 pounds (57 kg). Females
typically grow much larger than males. They are a migratory species, migrating north in
the summers and south in the winters, and migrating into rivers during the spring to
spawn. Females mature at age four, and males at age two; females will produce millions
of eggs which they release into riverine spawning areas where they are fertilized by
males. The eggs will drift downstream and eventually form into larvae. The larvae will
mature into juveniles in nursery areas, which are usually located in river deltas, and
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inland portions of coastal sounds and estuaries. After two years in these estuarine
habitats, they will join the migratory coastal population in the Atlantic Ocean. Once
mature, the fish will migrate to spawning areas in the spring (ASMFC 2008a).
Frequently, male striped bass remain along the coast near the area where they were
hatched, even after they mature, while females migrate much greater distances; Collette
and Klein-MacPhee (2002) note that only about 10% of the striped bass found in
northern waters are male. Young striped bass less than three years of age (sometimes
referred to as “schoolies” by anglers) are found in small groups, while larger striped bass
are found in large schools. Occasionally large females will be solitary (Ross 1991).
Mycobacteriosis is a disease affecting striped bass that may be having an influence on
mortality levels of this species; see Section 550.8 for more information on
mycobacteriosis.
Habitat
3. Striped bass spawn in riverine areas, usually in fresh or nearly fresh waters, and the
larvae will travel downstream to river deltas or the inland portions of coastal sounds and
estuaries, where they will mature. The majority of striped bass found off Rhode Island
will spawn within the Chesapeake Bay (ASMFC 2008a); some will also be fish born in
the Hudson River, which rarely migrate beyond Cape Cod (Ross 1991). Typically, the
fish spend their winters offshore between New Jersey and North Carolina. Striped bass
rarely stray from within six or eight kilometers (three to five miles) of the shore, and are
typically found along sandy beaches, in shallow bays, around rocks and boulders, and at
the mouths of estuaries (Collette and Klein-MacPhee 2002). Striped bass feed on a wide
variety of invertebrates, especially crustaceans, and on small fish.
Fishery
5. The striped bass fishery has been one of the most important Atlantic coast fisheries for
centuries and is one of the most popular recreational fisheries in the Ocean SAMP area.
Recreational fishermen take striped bass with hook-and-line, whereas in commercial
fisheries they are also taken with gillnets, pound nets, haul seines, and trawls. In Rhode
Island, commercial fishermen also use floating fish traps to catch striped bass, but are
prohibited from using gillnets for harvest in state waters. In 2006, commercial harvest
accounted for 17% of fish removals, while commercial discards of dead fish accounted
for 3%. Recreational harvest accounted for 45% of removals of striped bass, and
recreational discards of dead fish accounted for an additional 34%. In Rhode Island,
recreational vastly outweighs commercial harvest: in 2008, 732,564 pounds (332,285 kg)
were harvested by recreational fishermen whereas 245,988 pounds (111,578 kg) were
harvested by commercial fishermen (ASMFC 2008b). The striped bass populations
declined sharply in the 1970s and 1980s, causing many states to close their striped bass
fisheries. At present, the species is not overfished and overfishing is not occurring
(ASMFC 2008a). The amount of female striped bass capable of reproduction, known as
female spawning stock biomass, was estimated at 55 million pounds (25,000 metric tons)
for 2004, which is well above the recommended biomass threshold of 30.9 million
pounds (NMFS 2010b). Spawning stock biomass in 2004 was 42% greater than the target
level (NEFSC 2006a). Striped bass are managed by the Atlantic States Marine Fisheries
Commission through the Interstate Fishery Management Plan for Atlantic Striped Bass.
Commercial fisheries are managed through effort restrictions such as size limits and
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quotas, while recreational fisheries are managed through size limits, bag limits, and
fishing seasons (ASMFC 2008a).
Table 5.24. Habitat characteristics of striped bass. (Ross 1991; Collette and Klein-MacPhee 2002)
Life Stage
Habitat
Substrate
Temperature
Eggs
Released into riverine areas, drift
downstream.
Pelagic
Hatch from 14 to 22ºC.
Larvae/Juveniles
River deltas, inland portions of
estuaries. Remain in natal estuary
during first two years of their lives.
Sandy beaches,
rocky areas,
among rocks and
boulders.
N/A
Adults
Found within several miles of
shoreline, often in river mouths,
estuaries, or along rocky shorelines
and sandy beaches. Reproduce in
rivers or brackish areas of estuaries.
Sandy beaches,
rocky areas,
among rocks and
boulders, mussel
beds.
Spawning takes place
when water is about
18ºC. Migrate south
when water temperatures
reach 7ºC.
510.2.22. Summer Flounder (Paralichthys dentatus)
1. Summer flounder, also called fluke, are found in both inshore and offshore waters from
Nova Scotia to Florida, although they are most abundant from Cape Cod south to Cape
Fear, North Carolina. They are left-eyed flatfish, meaning the eyes are on the left side
when viewed from above, with the top fin facing up, distinguishing them from winter
flounder, which are right-eyed (ASMFC 2008a). In the Ocean SAMP area, summer
flounder are targeted by both commercial and recreational fishermen.
Life History
2. Summer flounder reach sexual maturity at age two or three, when they are about ten
inches (25 cm) in length. The fish spawn offshore in the fall; the oldest, largest fish
migrate, and thus spawn, first, followed by the smaller fish. The larvae will migrate
inshore to coastal and estuarine areas from October through May. Upon reaching the
coast, the larvae will move to the bottom, and spend the first year of their lives in bays
and other inshore areas. Summer flounder are born with eyes on both sides of their body,
but the right eye will migrate to the left side within 20-32 days (ASMFC 2008a). Females
are typically much larger than males and can grow up to three feet (0.9 m) in length and
weigh up to 29 pounds (13 kg) (Collette and Klein-MacPhee 2002). Females can live for
up to twenty years, although males rarely live more than seven years (Ross 1991).
Habitat
3. Summer flounder are concentrated in bays and estuaries from late spring through early
fall, when they migrate offshore to the continental shelf to waters between 120 to 600
feet (37 to 183 meters) in depth, spending their fall and winters offshore. The summer
flounder found off New England spend the winters east of the Hudson Canyon off New
York and New Jersey (Ross 1991). Adult summer flounder spend most of their lives near
the bottom, and prefer to bury themselves in sand substrate. During the summer, they are
often found on hard sand, and prefer mud during the fall. They are often found hiding
motionless in eelgrass or among the pilings of docks, but swim very quickly if disturbed
(Collette and Klein-MacPhee 2002).
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4. Summer flounder feed by waiting for their prey and then ambushing them. Summer
flounder have well-developed teeth that allow them to capture such prey as small fish,
squid, sea worms, shrimp, and other crustaceans (ASMFC 2008a). They are fierce
predators, pursuing prey up to the surface and sometimes jumping out of the water while
chasing prey, although they also feed on the bottom (Collette and Klein-MacPhee 2002).
Fishery
5. Summer flounder are one of the most sought-after species for both commercial and
recreational fishing along the East Coast. The species is currently managed under a joint
management plan between the Atlantic States Marine Fisheries Commission and the
Mid-Atlantic Fisheries Management Council as part of the Summer Flounder, Scup, and
Black Sea Bass Fishery Management Plan. The current plan by the Atlantic States
Marine Fisheries Commission allocates 60% of the quota to commercial fishing and 40%
to recreational fishing (ASMFC 2008c). Fishing mortality of summer flounder has been
declining and spawning stock biomass has been increasing since the 1990s. According to
the Atlantic States Marine Fisheries Commission, summer flounder is not currently
overfished, and overfishing is not occurring, although the stock is not yet rebuilt
(ASMFC 2008c). Summer flounder has been under a rebuilding plan since 1993, which
was recently extended to 2013. Biomass was estimated at about 77% of the target level in
2008, or about 46,029 metric tons (NMFS 2010b).
Table 5.25. Habitat characteristics of summer flounder. (NEFSC 1999e)
Life Stage
Habitat
Substrate
Temperature
Eggs
Eggs are pelagic and buoyant,
mostly at depths of 30-70 m in
the fall, as far down as 110 m
in the winter, and from 10-30
m in the spring.
Pelagic
Most abundant in the
water column where
bottom temperatures are
between 12 and 19ºC.
Larvae
Planktonic; most abundant 19-
83 km from shore at depths of
around 10-70 m. From October
to May larvae and postlarvae
migrate inshore to coastal and
estuarine nursery areas.
Dominant in sandy substrates
or where there was a transition
from fine sand to silt and clay.
Larvae have been found
in temperatures ranging
from 0-23ºC, but are
most abundant between
9 and 18ºC.
Juveniles
Juveniles are distributed
inshore and in many estuaries
throughout their range during
spring, summer, and fall.
Dominant in sandy substrates
or in transition areas from fine
sand to silt and clay. Juvenile
and adult summer flounder
will hide in vegetation to
ambush prey.
Most juveniles are
caught over a range of
temperatures from 10-
27ºC in the fall, from 3-
13ºC in the winter, from
3-17ºC in the spring,
and from 10-27ºC in the
summer.
Adults
During spring distributed
widely over the continental
shelf, from 0-360 m depth.
Found in depths of less than
100 m in summer and fall.
Generally are found at depths
greater than 70 m in winter.
Prefer sandy habitats; can be
found in a variety of habitats
with both mud and sand
substrates, including marsh
creeks, seagrass beds, sand
flats, among dock pilings.
Summer flounder will hide in
vegetation to ambush prey.
Most adults are caught
over a range of
temperatures from 9-
26ºC in the fall, from 4-
13ºC in the winter, from
2-20ºC in the spring,
and from 9-27ºC in the
summer.
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510.2.23. Tautog (Tautoga onitis)
1. Tautog, also called blackfish, are distributed along the coast of the Northwest Atlantic
from Nova Scotia through Georgia, with the greatest abundance found between Cape
Cod and the Chesapeake Bay. In the Ocean SAMP area, tautog are pursued primarily by
recreational fishermen, with a small commercial fishery in the area as well.
Life History
2. Both male and female tautog reach sexual maturity at three or four years of age, and
fecundity increases with size. Spawning takes place from May though August. Once they
have reached sexual maturity, many fish will return to the same spawning area
throughout their lives. Fertilized eggs will float for about two days before hatching.
Within four days of hatching, larvae will begin to feed on microscopic plankton. Tautog
are very slow growing. They can live up to 34 years and weigh up to 22 pounds (10 kg),
although the average fish is usually between six and ten years old, and weighs between
two and four pounds (one and two kilograms). Males grow larger and generally live
longer than females (Ross 1991). Tautog have been observed to leave a home area during
the daytime to feed, and then return to that home area throughout the night (Collette and
Klein-MacPhee 2002).
Habitat
3. Tautog usually spend their summers in shallow, coastal waters, and move offshore to
deeper waters in the fall. The fish migrate inshore to coastal waters and estuaries in the
spring when the water temperatures reach around 48 degrees Fahrenheit (9 degrees
Celsius). In the northern parts of their range, tautog remain inshore during the summer,
and are frequently found in waters less than 60 feet (18 m) deep south of Cape Cod,
although they may be found as far as 40 miles (64 km) from shore. They move offshore
to deeper waters during the fall, generally to between 80 and 150 feet (24 to 46 meters) in
depth, to spend the winter. Tautog spawn in the summer months, usually in water
temperatures between 62 and 70 degrees Fahrenheit (17 and 21 degrees Celsius), and in
areas dominated by eelgrass beds. Small juveniles seek out vegetated estuaries and other
inshore areas, while larger juveniles and adults are found in deeper offshore waters, often
preferring rocks and boulders, as well as piers, jetties, and mussel and oyster beds.
Inshore they are often found around the mouths of estuaries and other inlets (ASMFC
2008a). The fish will often follow flood tides inshore to feed in the intertidal zone,
moving to deeper water with the ebb tides (Ross 1991). Tautog will have a home site
which they will remain close to, moving away during the day to feed, and returning to at
night (ASMFC 2008a). They feed largely on invertebrates, including mussels, clams,
crabs, amphipods, shrimp, sand dollars, small lobsters, and barnacles. Some individuals
living near the shore feed largely on blue mussels, using their large teeth to tear the
mussels from the substrate, and then grinding the mussels in their teeth before
swallowing them (Ross 1991).
Fishery
4. The fishery for tautog is primarily recreational, accounting for about 90% of the fishery,
although there is also a commercial fishery for this species in Rhode Island waters and
elsewhere. Slow growth and reproduction rates, along with their tendencies to be found
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around rock piles, make tautog susceptible to overfishing. The species is managed by the
Atlantic States Marine Fisheries Commission through the Interstate Fishery Management
Plan for Tautog, which employs a minimum size limit. In addition, Rhode Island
employs a self-imposed commercial quota which is managed in three seasons; the
recreational fishery is managed by seasons and bag limits (RIDEM 2009). According to
the Atlantic States Marine Fisheries Commission, the stock is currently considered
overfished, but overfishing is not occurring (ASMFC 2008a). However it should be noted
that Rhode Island and Massachusetts assess tautog on a regional basis and are therefore
not bound to the coastwide assessment stock status. The most recent regional stock
assessment update indicates that the regional stock is overfished and overfishing is
occurring in RI and MA state waters (RIDEM 2010a).
Table 5.26. Habitat characteristics of tautog. (Ross 1991)
Life Stage
Habitat
Substrate
Temperature
Eggs
Eggs are buoyant.
Pelagic
17 - 21ºC
Larvae
N/A
Pelagic
N/A
Juveniles
Young tautog rarely stray from their
home sites. Small juveniles seek out
vegetated estuaries.
Steep, rocky
shorelines,
wrecks, mussel
and oyster beds,
boulders,
vegetated
estuaries.
N/A
Adults
Usually within 16 to 19 km of shore
and in water depths of 18 to 24 m.
Found in association with cover.
Spawn inshore over eelgrass beds.
Steep, rocky
shorelines,
wrecks, mussel
and oyster beds,
boulders.
Peak spawning from 17 to
21ºC. Migrate inshore
when water approaches
9ºC.
510.2.24. Tuna, Bluefin (Thunnus thynnus)
1. In the Ocean SAMP area, tuna are targeted primarily by recreational fishermen and were
historically a major focus of Rhode Island sportfishing tournaments. The tuna species
targeted recreationally in Rhode Island waters include the yellowfin tuna and bluefin
tuna. Both species are important in commercial fisheries elsewhere around the globe.
Life History
2. The bluefin tuna is the largest species of bony fish in the world. Bluefin tuna are found
both in schools and individually. They are generally classified into three size groups:
juvenile or school tuna (5 to 70 pounds / 2 to 32 kg); medium tuna (70 to 270 pounds / 32
to 122 kg); and giant tuna (greater than 270 pounds / 122 kg). While bluefin tuna are
found in both the Atlantic and Pacific Oceans, as well as the Mediterranean, Atlantic
bluefin tunas grow to the largest size, reaching lengths of ten feet or greater and
sometimes weighing more than 1,000 pounds (454 kg). A bluefin tuna reaches sexual
maturity at about six years of age, and they can live up to 38 years of age. Giant bluefin
tunas will spawn in the Caribbean and Gulf of Mexico from April through June before
heading north, while mid-sized tuna spawn later in the year, and may spawn as far north
as the New York Bight. Like yellowfin tuna, bluefin tuna are warm-blooded, permitting
them to withstand large fluctuations in temperature, and to maintain very high swimming
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speeds over a long period (Ross 1991). This fish is known for making long migrations,
and fish tagged off North America have been found off Europe and Africa.
Habitat
3. Bluefin tuna, a pelagic species, are rarely found at depths greater than 300 feet (91 m)
and are sometimes seen at the surface of the water. The species migrates along the
Atlantic coast, moving northward and inshore during the spring and summer, and then
offshore and to the south during the fall. Large bluefin tunas will sometimes be found in
waters as cold as 50 to 54 degrees Fahrenheit (10 to 12 degrees Celsuis), but smaller fish
prefer temperatures above 60 degrees Fahrenheit (16 degrees Celsius). Giant bluefin
tunas appear in New England waters before smaller individuals, mostly in June and July.
Small bluefin tunas will appear in southern New England later in July (Ross 1991). The
fish can be found in Rhode Island waters through November, although they are most
common in July. Small school tunas are relatively common off Rhode Island during the
summer, although giant bluefin tuna are rare (Collette and Klein-MacPhee 2002). The
bluefin tuna is a noted predator, feeding on schooling species such as herring, mackerel,
squid, and silver hake (Ross 1991).
Table 5.27. Habitat characteristics of bluefin tuna. (Ross 1991)
Life Stage
Habitat
Substrate
Temperature
Juveniles
Both inshore and offshore areas,
rarely found more than 90 meters
below the surface.
Pelagic
Stay in waters above
16ºC
Adults
Both inshore and offshore areas,
rarely found more than 90 meters
below the surface. Follow the
Gulf Stream.
Pelagic
Waters as cold as 10 to
12ºC
Fishery
4. In the Ocean SAMP area, bluefin tuna are targeted primarily by recreational fishermen.
Bluefin tuna are managed domestically by the NMFS Consolidated Atlantic Highly
Migratory Species Management Plan and internationally through the International
Commission for the Conservation of Atlantic Tunas. The allocation of bluefin tuna in the
United States is divided into five categories: a purse seine fishery, a harpoon fishery, a
general category fishery (including hook-and-line, handline, and harpoon vessels), an
incidental-catch fishery for vessels targeting other species or bluefin tuna of another size
from one of the other categories, and an angling fishery for smaller bluefin tunas (Ross
1991). At one time, Galilee was known as the Tuna Capital of the World, and was home
to the Atlantic Tuna Tournament, until the tournament was moved to Gloucester in 1973
(Olsen and Stevenson 1975). Bluefin tuna is considered overfished, and overfishing is
occurring. Two different stock assessment scenarios place the spawning stock biomass of
bluefin tuna at either 14% or 57% of target levels (NMFS 2010b). In 2010, there was a
proposal to list bluefin tuna in Appendix 1 of the international Convention for the
International Trade of Endangered Species (CITES), which would indicate the species
was threatened with extinction and international commercial trade would be restricted.
This proposal was not accepted at the most recent CITES convention, but there is
growing international concern over the stock status of bluefin tuna (CITES 2009, CITES
2010).
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510.2.25. Tuna, Yellowfin (Thunnus albacares)
1. Yellowfin tuna is another tuna species targeted in the Ocean SAMP area by recreational
fishermen. Like bluefin tuna, it is important in commercial fisheries elsewhere around the
globe.
Life History
2. Yellowfin tunas, like other tunas, are warm-blooded, maintaining an internal body
temperature that may be much higher than the external water temperature, permitting
them to swim at higher speeds and for longer periods than other fish. Yellowfin tuna
form schools with other individuals of a similar size, sometimes with similarly-sized tuna
of other species. Tunas spawn throughout the year, with peaks during the summer
months in the northern parts of their range. Some yellowfin tuna will mature at twelve to
fifteen months of age, when they are between 20 and 24 inches (50 and 60 cm) in length,
while others may not mature until they are at least 47 inches (145 cm) in length. The fish
grow quickly, to about 21 inches (53 cm) by their first year, and reaching lengths of over
six feet (1.8 m) (Ross 1991).
Habitat
3. The yellowfin tuna occurs along the edge of the continental shelf from Nova Scotia south
through both temperate and tropical waters. The yellowfin is an open-ocean, schooling
tuna found throughout the water column, usually in temperatures between 65 and 88
degrees Fahrenheit (18 and 31 degrees Celsius). They prefer waters of at least 68 degrees
(20 degrees Celsius), and water temperature determines where this fish is found both
geographically and also within the water column. Schooling usually occurs near the
surface, and large schools are often found in major upwelling areas. After they hatch,
larvae will remain in the upper 200 feet (61 meters) of the water column. Yellowfin
usually feed during the daylight hours close to the surface. They eat a variety of finfishes,
cephalopods, and crustaceans (Ross 1991).
Table 5.28. Habitat characteristics of yellowfin tuna. (Ross 1991)
Life Stage
Habitat
Substrate
Temperature
Juveniles/Adults
Open-ocean species, found
throughout upper water column.
Temperature determines where it is
found in water column. Often
found in areas of upwelling.
Pelagic
Between 18 to 31ºC
Fishery
4. Yellowfin tuna are managed domestically by the NMFS Consolidated Atlantic Highly
Migratory Species Management Plan and internationally through the International
Commission for the Conservation of Atlantic Tunas. Management measures include a
recreational retention limit (NMFS 2010b). Both yellowfin and bluefin tuna have
historically been important to recreational fisheries in Rhode Island and were once the
focus of multiple Rhode Island-based fishing tournaments. Recreational fishermen target
yellowfin tuna using longline, handline, and rod and reel gear. The biomass level of
Atlantic yellowfin tuna is currently considered to be at 96% of the level needed for
maximum sustainable yield, and overfishing is not occurring (NMFS 2010b).
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510.2.26. Winter Flounder (Pseudopleuronectes americanus)
1. Winter flounder, also called blackback flounder or lemon sole, are a right-handed flat
fish found in shallow, estuarine habitats along the Northwest Atlantic coast. In the Ocean
SAMP area, winter flounder are targeted by both commercial and recreational fishermen.
Life History
2. Winter flounder spawn in the winter and early spring, producing both demersal eggs and
adhesive eggs (ASMFC 2008a). The eggs hatch about fifteen to eighteen days after being
released (Ross 1991). Larvae will be found in the upper reaches of estuaries in early
spring, and will move to the lower estuary as they grow (ASMFC 2008a). Studies of the
genetic population structure of winter flounder larvae and juveniles in Narragansett Bay
found that juvenile flounder tend to remain near their natal nursery grounds (Buckley et
al. 2008). Winter flounder generally reach sexual maturity by age three (Ross 1991).
Winter flounder depend on sight to feed, and therefore feed only during the day. At night
they lie flat on the bottom and retract their eye turrets (ASMFC 2008a). They typically
lie buried in the mud with only their eyes showing, but can dash quickly for a few yards
when feeding. Adults are typically between twelve and fifteen inches long (30 to 38 cm),
and weigh between a pound and a half and two pounds (0.6 and 0.9 kg), although fish as
long as 25 inches (63 cm) have been recorded (Collette and Klein-MacPhee 2002).
Winter flounder can live for about twelve years (Ross 1991).
Habitat
3. Winter flounder get their name because they migrate into nearshore waters in the winter
months. They prefer muddy sand habitat inshore, particularly eelgrass habitat. Many
winter flounder move into estuarine habitats in the fall prior to spawning, typically
spawning on shallow, sandy bottom, and move either offshore or to deeper, cooler
portions of estuaries during the spring and summer (ASMFC 2008a). They are rarely
found deeper than 180 feet (55 m), although have been found as deep as 420 feet (128 m)
on Georges Bank (Ross 1991). Important nursery habitats for larvae and juveniles
include saltwater coves, coastal salt ponds, embayments, and estuaries, although some
larvae and juveniles have been found in the open ocean (ASMFC 2008a). Winter
flounder are known to return to the same pond or portion of the Bay where they were
hatched (Collette and Klein-MacPhee 2002). They are found in both Narragansett Bay
and the Sounds off Rhode Island.
4. Winter flounder have a small mouth, and feed on small invertebrates, shrimp, clams, and
worms. Larval flounder eat primarily diatoms (Collette and Klein-MacPhee 2002). In
turn, adult winter flounder are prey for a number of species including cod, dogfish,
monkfish, skates, hakes, striped bass, bluefish, and other fish. The larvae and juveniles
are preyed upon by striped bass, bluefish, and summer flounder, as well as birds,
invertebrates, and marine mammals (ASMFC 2008a).
Fishery
5. Winter flounder are targeted in both commercial and recreational fisheries; recreational
harvest has traditionally made up a significant percentage of total harvest levels for this
species (Ross 1991). However, in the most recent decade the recreational harvest has
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been severely limited by regulation, and at present there is a two-fish bag limit for winter
flounder. For management purposes, there are considered to be three stocks of winter
flounder: the Gulf of Maine, Georges Bank, and Southern New England/Mid-Atlantic
Bight stocks. The Southern New England/Mid-Atlantic Bight stock of winter flounder is
currently considered overfished and experiencing overfishing. The stock of winter
flounder has declined considerably from a combination of overfishing and habitat
degradation, a threat to which winter flounder are particularly susceptible given the fact
that they spawn in vulnerable near-shore habitats. According to the Atlantic States
Marine Fisheries Commission, winter flounder is currently overfished, and overfishing is
occurring. In 2007, the Southern New England/Mid-Atlantic Bight spawning stock
biomass (SSB) was estimated at 7.4 million pounds (3.4 million kg), or 9% of the target
SSB for this species. Fishing mortality in 2007 was at 262% of the plan target; presently,
even if fishing mortality were reduced to zero, the stock would not be rebuilt by the
current 2014 target (ASMFC 2008a). The stock is jointly managed by the Atlantic States
Marine Fisheries Commission and the New England Fishery Management Council,
employing fishing effort controls including seasonal closures, gear restrictions, size
limits, trip limits, and days-at-sea restrictions. In addition, NMFS has recently
implemented new groundfish rules which prohibit vessels from keeping southern New
England winter flounder (NMFS 2010b). Because the area winter flounder seem to be
made up of several local, genetically distinct populations, each of which returns to its
own spawning ground, this puts the species at greater risk for localized losses. In the
event that a spawning aggregation is lost to fishing or other factors, this localized
population is unlikely to be able to rebuild (Buckley et al. 2008).
Table 5.29. Habitat characteristics of winter flounder. (NEFSC 1999f)
Life Stage
Habitat
Substrate
Temperature
Eggs
Found at 0.3-4.5 m (inshore); 90 m or less on
Georges Bank.
Mud to sand
or gravel.
Spawning initiated at about
3ºC; highest percent hatch at
3-5ºC; 18ºC lethal.
Larvae
1-4.5 m inshore. Salt water coves, salt ponds,
estuaries, embayments.
Fine sand,
gravel.
Hatch from 1-12ºC; larvae
most abundant at 2- 15ºC.
Juveniles
Peak abundance of flounder less than 200 mm
occurs in 18-27 m of water in Long Island
Sound in April and May. Less than 100 m
offshore.
Equally
abundant on
mud or sand
shell.
Commonly found at 10-
25ºC during summer and fall.
Adults
Most 1-30 m inshore, shallowest during
spawning; less than 100 m offshore. Rarely
deeper than 60m.
Mud, sand,
cobble, rocks,
boulders, eel
grass.
0.6-23ºC; 12-15ºC suggested
as preferred.
510.2.27. Yellowtail Flounder (Limanda ferruginea)
1. The yellowtail flounder is distributed from Labrador to the Chesapeake Bay. There are
three stocks of yellowtail flounder for management purposes – the Cape Cod/Gulf of
Maine, Georges Bank, and Southern New England/Mid-Atlantic stocks (NEFSC 2006a).
Within the Ocean SAMP area, yellowtail flounder have traditionally been pursued by
commercial fishermen.
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Life History
2. Yellowtail flounder grow to about twenty-two inches (56 cm) and weigh up to 2.2
pounds (1 kg). Yellowtail flounder are sexually dimorphic, with females growing faster
than males. Female fish reach sexual maturity at a median of 1.6 years of age off
southern New England (NEFSC 1999g). Spawning occurs in spring and summer,
peaking in May. Eggs are deposited on or near the bottom, and then float to the surface
once fertilized. The larvae drift for about two months before settling to the bottom
(NEFSC 2006a). Fish from the southern New England stock of yellowtail flounder
typically remain within their fishing grounds, but migrate eastward during spring and
summer, and then westward during fall and winter as water temperatures change
(NEFSC 1999g).
Habitat and prey
3. Yellowtail flounder are found south of Block Island all year long, and in shallower
waters during the winter. They prefer sand and sand-mud bottoms between 33 and 330
feet (10 and 100 m), and are most abundant at temperatures between 46 and 57 degrees
Fahrenheit (8 and 14 degrees Celsius) (NEFSC 1999g). They generally avoid rocky areas
or soft mud (Collette and Klein-MacPhee 2002). Yellowtail flounder eat small
crustaceans, polychaetes, and sand dollars (NEFSC 1999g).
Fishery
4. Yellowtail flounder are managed under the New England Fishery Management Council’s
Northeast Multispecies Fishery Management Plan, along with fourteen other groundfish
species. They are managed through fishing effort limitations which include gear
restrictions, time/area closures, minimum size limits, a moratorium on permits, and days-
at-sea. The fishery for yellowtail flounder off southern New England developed in the
1930s, and the stock collapsed in the early 1990s. Spawning biomass has remained low
since then. Discards constitute about twenty percent of the catch. At present, the stock is
considered overfished, and overfishing is presently occurring. The biomass of the
southern New England/Mid-Atlantic stock of yellowtail flounder is estimated to be at
13% of targeted levels, or about 3,500 metric tons in 2007 (NMFS 2010b).
Table 5.30. Habitat characteristics of yellowtail flounder. (NEFSC 1999g)
Life Stage
Habitat
Substrate
Temperature
Eggs
Pelagic, near surface, along continental shelf
waters of Georges Bank, northwest of Cape
Cod, southern New England and nearshore
along NJ and southern Long Island.
Pelagic
Range 2.0-15°C
Larvae
Pelagic, movement limited to water current.
Peak during May-July in southern New England
and southeastern Georges Bank.
Pelagic
Range 5.0-17°C
Juveniles
Spring and Fall: In Gulf of Maine
concentrations occur between Mass. Bay, Cape
Cod, and along the outer perimeter of Cape
Cod. Southern edge of Georges Bank in spring.
Sand or sand
and mud.
2.0-16°C in Spring,
5.0-18°C in Fall.
Adults
High concentrations around Cape Cod for both
spring and autumn seasons. Concentrations pull
away from coastal southern New England, Long
Island, and the NY Bight during autumn
Sand or sand
and mud. Avoid
rocky areas or
soft mud.
2.0-16°C in Spring,
5.0-18°C in Fall.
Spawning: estimated
range 2.0- 17°C
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months. Spawning along continental shelf
waters of Georges Bank, northwest of Cape
Cod, southern New England and nearshore
along NJ and southern Long Island, peaks in
April to June in southern New England. Prefer
depths between 9 to 110 m.
510.3. Stocks of Concern
1. Several of the above-mentioned finfish species include regional stocks that are of
particular management concern within the vicinity of the Ocean SAMP area and adjacent
waters. Those stocks include the Georges Bank and southward stock of cod (which
includes cod found in Ocean SAMP waters) and the Southern New England/Mid-Atlantic
winter flounder and yellowtail flounder stocks, all managed by the New England Fishery
Management Council. These also include butterfish, which is managed by the Mid-
Atlantic Fishery Management Council. Each of these stocks has additional management
measures in place. Incidental catch quotas are in place for each of the New England
Fishery Management Council-managed stocks, meaning that in addition to other
multispecies regulations, there is a limit to how many fishermen can catch while
targeting other species. Management of butterfish by the Mid-Atlantic Fishery
Management Council has recently changed significantly to address butterfish bycatch.
These stocks are further discussed below.
510.3.1. Georges Bank and Southward Cod6
1. The Georges Bank and southward stock of cod, which includes cod found in southern
New England, is managed by the New England Fishery Management Council. Both the
Georges Bank and Gulf of Maine stocks of cod have declined since the 1960s and are in
the process of being rebuilt. Currently, the Georges Bank and southward cod stock is at
10% of the level needed to achieve maximum sustainable yield. According to the most
recent stock assessment, biomass levels for the Gulf of Maine stock have increased
substantially such that this stock is no longer considered overfished, whereas biomass
levels for the Georges Bank stock have not changed much since an earlier stock
assessment in 2004. In 2007, spawning stock biomass was estimated at 17,672 metric
tons, a relatively small increase over 2004 estimates (NEFSC 2008).
2. Cod are managed under the Northeast Multispecies Fishery Management Plan, which
encompasses most species in the groundfish complex. Through the Fishery Management
Plan, area closures, gear restrictions, and minimum size limits have been employed as the
primary management tools. In 2004, the controversial Amendment 13 to the Fishery
Management Plan was implemented, with tighter regulations on catch in an attempt to
reduce mortality on this species. The Georges Bank stock of cod is a transboundary
resource shared with Canada, which is responsible for managing a portion of the stock as
well. Generally about 25% of the annual catch is taken by Canadian vessels, with the rest
6 NMFS assesses and manages Atlantic cod as two distinct stocks, the “Gulf of Maine” stock and the “Georges Bank
and Southward” stock (NMFS 2010b). It should be noted that cod found in southern New England, including the
Ocean SAMP area, are part of the Georges Bank and Southward stock.
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taken by American vessels (Mayo and O’Brien 2006). As of May 1, 2010, NMFS
implemented additional catch limits and other management measures to further protect
cod and other groundfish stocks (NMFS 2010b).
510.3.2. Southern New England/Mid-Atlantic Winter Flounder
1. The Southern New England/Mid-Atlantic stock of winter flounder is managed by the
New England Fishery Management Council. According to the 2008 stock assessment,
winter flounder stocks have severely declined. In 2007, the spawning stock biomass of
Southern New England/Mid-Atlantic winter flounder was approximately 3,368 metric
tons, or 9% of the target level. This was an increase from 2005 levels, which were a
record low of 2,098 metric tons. Commercial landings of Southern New England winter
flounder peaked in 1966 and again in 1981, then falling to a record low of 1,320 metric
tons in 2005. Landings had increased somewhat by 2007, reaching 1,622 metric tons
(NMFS 2010b).
2. Winter flounder are managed under the Northeast Multispecies Fishery Management
Plan, which encompasses most species in the groundfish complex. Through the Fishery
Management Plan, effort controls (days at sea), area closures, gear restrictions, and
minimum size limits have been employed as the primary management tools. In 2004, the
controversial Amendment 13 to the FMP was implemented, with tighter regulations on
catch in an attempt to reduce mortality on this and other groundfish species (NMFS
2010b). In state waters, they are managed through the Atlantic States Marine Fisheries
Commission’s Fishery Management Plan for Inshore Stocks of Winter Flounder.
Management measures under the Atlantic States Marine Fisheries Commission plan
include a two-fish bag limit for recreational fishermen, and a 50 pound possession limit
for non-federally permitted commercial fishermen (ASMFC 2008a). Recently, NMFS
has also implemented new groundfish rules which include additional protections for
winter flounder, including a prohibition against keeping winter flounder (NMFS 2010b).
510.3.3. Southern New England/Mid-Atlantic Yellowtail Flounder
1. The Southern New England/Mid-Atlantic stock of yellowtail flounder is managed by the
New England Fishery Management Council. The spawning stock biomass of Southern
New England/Mid-Atlantic yellowtail flounder is currently at 13% of the target levels
needed to support maximum sustainable yield (NMFS 2010b). The fishery for yellowtail
flounder in Southern New England began in the 1930s, and landings peaked in the 1960s;
by the mid-1990s the fishery had collapsed. Between 1994 and 2005, spawning stock
biomass generally averaged around 1,100 metric tons, but increased to 3,500 metric tons
in 2007. Landings of Southern New England yellowtail flounder reached a record low of
200 metric tons in 1995, increased to over 1,000 metric tons in 2000 and 2001, and
declined again to 200 metric tons in 2006 and 2007 (NMFS 2010b).
2. Yellowtail flounder are managed under the Northeast Multispecies Fishery Management
Plan, which encompasses most species in the groundfish complex. Through the Fishery
Management Plan, effort controls (days at sea), area closures, gear restrictions, and
minimum size limits have been employed as the primary management tools. In 2004, the
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controversial Amendment 13 to the FMP was implemented, with tighter regulations on
catch in an attempt to reduce mortality on this and other groundfish species. Yellowtail
flounder are also directly managed through days-at-sea restrictions and a moratorium on
permits. As of May 1, 2010, NMFS implemented additional catch limits and other
management measures to further protect yellowtail flounder and other groundfish stocks
(NMFS 2010b).
510.3.4. Butterfish
4. Butterfish are managed by the Mid-Atlantic Fishery Management Council. Butterfish
biomass estimates vary considerably from year to year. From 1968 to 2002, the spawning
stock biomass ranged from 7,800 to 62,900 metric tons, although it has consistently
declined since 1980. U.S. commercial landings of butterfish peaked in 1984, and have
declined since then, reaching a low of 432 metric tons in 2005. Discards of butterfish in
other fisheries can be substantial, ranging from an estimated 1,000 to 9,200 metric tons in
recent years. From 1965 to 2002, commercial landings averaged 3,200 metric tons per
year, while discards averaged 5,300 metric tons per year (NEFSC 2006a).
2. Butterfish are managed by the Mid-Atlantic Fishery Management Council as part of the
Atlantic Mackerel, Squid, and Butterfish Fishery Management Plan. In 2005, butterfish
was listed as overfished. As a result the Atlantic Mackerel, Squid, and Butterfish Fishery
Management Plan was amended to address butterfish mortality resulting from bycatch
and discarding through a variety of management measures (MAFMC 2009).
510.4. Forage Fish
1. Commercial and recreationally targeted species rely on the availability of forage fish to
survive. The northern sand lance is an important forage fish found in Ocean SAMP
waters, and serves as an important prey species in southern New England for smooth
dogfish, winter skate, silver hake, Atlantic cod, summer flounder, windowpane, striped
bass, and yellowtail flounder (Bowman et al. 2000), as well as silversides and smelt.
Other important forage fish in the Ocean SAMP area were mentioned above in the
descriptions of commercially and recreationally important species, and include Atlantic
herring, squid (both long- and short-fin), and butterfish. Menhaden is another important
forage fish in this area (see above), as are alewife and blueback herring (see below under
“river herring”). Herring and menhaden in particular have been the subject of fisheries
management debates in recent years over how to consider their importance as a source of
food within the ecosystem for fish, seabird, and marine mammal species, while trying to
set catch targets to permit commercial fisheries.
510.5. Threatened and Endangered Species and Species of Concern
1. Several finfish species that may occur within the Ocean SAMP area are not targeted
through commercial or recreational fisheries, but may be managed by the NMFS Office
of Protected Resources. The NMFS Office of Protected Resources has jurisdiction over
most marine and anadromous species listed as endangered or threatened under the federal
Endangered Species Act (ESA). In addition, NMFS has identified "Species of Concern"
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as species about which NMFS has some concerns regarding status and threats, but for
which insufficient information is available to indicate a need to list the species under the
ESA (NMFS 20l0a. However, "Species of Concern" status does not carry any procedural
or substantive protections under the ESA. For further discussion of non-finfish species
protected under the Endangered Species Act, see Chapter 2, Ecology of the Ocean SAMP
Region.
2. According to the NMFS Northeast Regional Office Protected Resources Division, based
on the best available information, no finfish currently listed as threatened or endangered
are likely to occur within the Ocean SAMP area (Crocker, pers. comm. a). However,
according to the NMFS Northeast Regional Offices Protected Resources Division
(Crocker, pers. comm., b), the following species currently listed as “Species of Concern”
(NMFS 2010a) could be present in the Ocean SAMP area: Atlantic halibut (Hippoglossus
hippoglossus); Atlantic sturgeon (Acipenser oxyrinchus oxyrinchus); Atlantic wolffish
(Anarhichas lupus); Dusky shark (Carcharhinus obscurus); Porbeagle shark (Lamna
nasus); Rainbow smelt (Osmerus mordax); River herring (which includes two species:
Alewife (Alosa pseudoharengus) and Blueback herring (Alosa aestivalis)); Sand tiger
shark (Carcharias taurus); and Thorny skate (Amblyraja radiate).
510.5.1. Atlantic Halibut (Hippoglossus hippoglossus)
1. The Atlantic halibut is distributed from Labrador to southern New England and is one of
the largest fish found in the Gulf of Maine. There is currently no directed fishery for
halibut, but there was a major commercial halibut fishery in the Gulf of Maine
throughout the 19th century (NEFSC 2006a).
Life History and Habitat
2. Halibut are large, long-lived, right-eyed flounders. Females are typically larger than
males, growing to an average of 100-150 pounds (45.5-68 kg). Halibut mature at
approximately 10 years yet are prolific, with females spawning several batches of eggs
each year. Period of spawning varies by region, and the depth at which halibut spawn is
not known. Halibut eggs drift within the water column and hatch at a very immature
stage. Halibut are bottom-dwelling flat fish typically found on sand, gravel, or clay
bottom. They move into shallower waters in the summer and deeper waters in the winter,
and have been found in U.S. waters in trawls at temperatures ranging from 4-13°C (39-
55°F). Halibut prey for the most part on other fish, but also eat shellfish, crustaceans, and
even seabirds (Collette and Klein-MacPhee 2002).
Management
3. Atlantic halibut are managed by the New England Fishery Management Council under
their Multispecies Fishery Management Plan, which includes a moratorium on direct
harvests as well as bycatch limits and minimum fish sizes (NEFSC 2006a). Atlantic
halibut were heavily fished throughout the 19th century and have not recovered since, and
for this reason NMFS attributes the species’ decline to overfishing (NMFS 2009b).
According to NMFS, Atlantic halibut are listed as a species of concern because of
demographic and genetic diversity concerns (NMFS 2009b).
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510.5.2. Atlantic Sturgeon (Acipenser oxyrinchus oxyrinchus)
1. Atlantic sturgeon is an anadromous finfish found from Labrador to Florida. They are
ancient fish, dating back at least 70 million years (ASMFC 2009c). In addition to its
status as a species of concern, Atlantic sturgeon is a candidate for listing under the
Endangered Species Act (NMFS 2010c).
Life History and Habitat
2. The average Atlantic sturgeon ranges in size from 2.9-6.6 feet (88 – 200 cm) (Collette
and Klein-MacPhee 2002), although sturgeon have been known to grow up to 14 feet
(425 cm) with weights of more than 800 pounds (363 kg) (NMFS 2010c). Sturgeon may
live up to 60 years. There is significant variation in the age of sexual maturity, with fish
at the northern end of their range maturing later. Atlantic sturgeon are anadromous fish,
with adults migrating upriver in the spring to spawn. Spawning does not necessarily
occur every year, and sturgeon eggs adhere to benthic substrate (Collette and Klein-
MacPhee 2002). Sturgeon are bottom dwellers and prey upon shellfish, crustaceans, and
small fish (ASMFC 2009c).
Management
3. Historically, Atlantic sturgeon were harvested commercially for a wide range of
commercial uses of both the fish and its eggs. ASMFC instituted a coast-wide
moratorium prohibiting the harvest and retention of Atlantic sturgeon in 1998, and
NMFS followed with a moratorium in Federal waters. According to NMFS, Atlantic
sturgeon were first identified as a species of concern in 1988; however, they were
formally retained on the list in 1998. According to NMFS, Atlantic sturgeon numbers
have declined because of fishing pressure as well as incidental mortality through bycatch,
habitat degradation, and dams that have interrupted spawning behavior. In October 2009,
the Natural Resources Defense Council petitioned NMFS to list the Atlantic sturgeon
under the Endangered Species Act. At the time of this writing, NMFS is in the process of
developing a listing determination indicating whether listing Atlantic sturgeon as an
endangered or threatened species is warranted (NMFS 2010c). This decision must be
published in the Federal Register on or before October 6, 2010 (12 months after receipt
of the NRDC petition).
510.5.3. Atlantic Wolffish (Anarhichas lupus)
1. Atlantic wolffish are sedentary, solitary fish that are primarily taken as bycatch in other
fisheries. They are known for their canine-like teeth and biting ability.
Life History and Habitat
2. Atlantic wolffish are large, slow growing fish known for their large teeth. They may
grow up to 59 inches (150 cm) long and 40 pounds (18 kg) and live up to 20 years. Males
and females form pairs before spawning, and females lay egg masses of varying sizes in
clusters in protected areas which are then protected by the males. Spawning period varies
by region (Collette and Klein-MacPhee 2002). Females may produce between 5,000 and
12,000 eggs, with larger females producing larger egg masses (NMFS 2009c). Atlantic
wolffish are benthic dwellers with a preference for complex habitats such as rocky areas.
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They can be found in depths up to 1640 feet (500 meters) and in waters as cold as 1.3°C
(34°F). They feed on a diverse diet of benthic fauna as well as a variety of shellfish,
crustaceans, and echinoderms (Collette and Klein-MacPhee 2002).
Management
3. Wolffish are frequently taken as incidental catch in otter trawl fisheries, and small
quantities of wolffish have been landed by commercial fishermen since the 1970s,
though catches have declined to a recent low (NEFSC 2006a). According to NMFS, the
decline of the wolffish can be attributed to incidental catch, as well as commercial
fishing, and habitat degradation caused by fishing gear. NMFS designated the Atlantic
wolffish a species of concern in 2004 due to demographic and genetic diversity concerns.
In 2008, NMFS was petitioned to list the Atlantic wolffish under the Endangered Species
Act, and in 2009, NMFS found that listing was not warranted at that time (NMFS
2009c). In 2010, Atlantic wolffish were added to the Northeast Multispecies Fisheries
Management Plan (FMP) in Amendment 16 to the plan. Inclusion of Atlantic wolffish in
Amendment 16 provides for the prohibition of landing Atlantic wolffish in commercial
and recreational fisheries.
501.5.4. Dusky Shark (Carcharhinus obscurus)
1. The dusky shark is a highly migratory large coastal shark that occurs from southern New
England to the Caribbean and South America.
Life History and Habitat
2. Dusky sharks reach an average size of 11.8 feet (360 cm) long and 400 pounds (180 kg)
and can live up to 40 years. Like many sharks, dusky sharks bear live young. They
reproduce every three years, bearing litters ranging from 6 to 14 young, which may range
in size from 33 to 39 inches (85-100 cm) (NMFS 2009d). The dusky shark is a highly
migratory species, migrating north in the summer and south in the fall and winter,
following warmer waters. Dusky sharks seem to avoid estuaries and other areas of lower
salinity (Collette and Klein-MacPhee 2002), and may be found from the surf zone to
offshore and from the surface to depths up to 1300 feet (400 m) (NMFS 2009d).
Management
3. Dusky sharks are managed as a highly migratory species by NMFS under the
Consolidated Atlantic Highly Migratory Species Fishery Management Plan and by the
Atlantic States Marine Fisheries Commission under the Interstate Fishery Management
Plan for Atlantic Coastal Sharks. According to NMFS, dusky sharks are currently
overfished. They have been a popular target for recreational fishermen, though they have
been harvested commercially and have also been taken as bycatch in directed fisheries.
Commercial and recreational fishing for dusky sharks has been prohibited since 1998.
NMFS attributes their decline to recreational fishing pressure and incidental mortality as
bycatch, and listed them as a species of concern in 1997 due to a range of demographic
and genetic diversity concerns (NMFS 2009d).
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501.5.5. Porbeagle Shark (Lamna nasus)
1. The porbeagle shark is a large coastal and oceanic shark found from Newfoundland to
New Jersey.
Life History and Habitat
2. The average porbeagle shark grows to between 4 and 6 feet (120-180 cm) in length,
though may reach a maximum size near 10 feet (300 cm) and may live up to 46 years
(Collette and Klein-MacPhee 2002). Porbeagle sharks give birth to live young, though
prior to birth the young are nourished in utero with egg yolk for roughly 8-9 months
(NMFS 2010d). Porbeagle shark are pelagic and infrequently enter shallow, coastal
waters (Collette and Klein-MacPhee 2002). Porbeagle sharks in the northwest Atlantic
are believed to make extensive annual migrations. They feed on small fish, other shark
species, and squid (NMFS 2010d).
Management
3. Porbeagle sharks were harvested commercially in the Northwest Atlantic starting in the
early 19th century (Collette and Klein-MacPhee 2002). Catch records indicate that the
fishery collapsed in the early 1960s and dropped off through the 1970s and 1980s,
allowing the population to rebuild. In the early 1990s a new fishery developed and catch
rates increased dramatically, only to drop off again. Porbeagle sharks are managed by
NMFS under the Consolidated Atlantic Highly Migratory Species Fishery Management
Plan and by the Atlantic States Marine Fisheries Commission under the Interstate Fishery
Management Plan for Atlantic Coastal Sharks. According to NMFS, porbeagle shark are
overfished, although overfishing is not currently occurring. NMFS attributes the decline
of porbeagle sharks to fishing pressure, and designated them a species of concern in 2006
(NMFS 2010d). In early 2010, NMFS received two petitions to list porbeagle sharks
under the ESA. After reviewing the petitions and available information, including the
most recent stock assessment from the International Commission for the Conservation of
Atlantic Tunas (ICCAT) and International Council for the Exploration of the Seas
(ICES), it was determined that the petitions did not present substantial scientific
information indicating that listing the species under the ESA may be warranted at this
time (75 Fed. Reg. 39656, 12 July 2010). In 2010, there was a proposal to list porbeagle
sharks in Appendix II of the Convention on the International Trade in Endangered
Species, though this proposal did not receive the votes that are needed to be passed
(CITES 2010).
510.5.6. Rainbow Smelt (Osmerus mordax)
1. Rainbow smelt are small, pelagic, anadromous fish found from Labrador to New Jersey.
Life History and Habitat
2. Rainbow smelt are small, slender fish, averaging 7 - 9 inches (18 – 23 cm) in length.
Rainbow smelt are anadromous and make their migrations upriver to spawn in the early
spring; they typically do not migrate far upstream and many spend most of their lives in
relatively shallow estuarine or coastal waters. Rainbow smelt typically begin spawning at
age two and a female can produce 7,000 to over 75,000 eggs depending on her size.
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Smelt often school during migrations, though little is known about smelt behavior while
at sea. Smelt feed on amphipods, shrimps, euphausiids, mysids, and marine worms, as
well as small fishes, and are themselves a major food source for larger fish as well as
aquatic birds (Collette and Klein-MacPhee 2002).
Management
3. Historically, rainbow smelt have been targeted by both commercial and recreational
fishermen, particularly in northern New England and Canada, and are still popular among
sport fishermen (Collette and Klein-MacPhee 2002). According to NMFS, rainbow smelt
populations have declined due to a variety of factors including fishing, dams and other
habitat degradation that impacts spawning behavior, and acid precipitation. Citing a
variety of demographic and genetic diversity concerns for this species in the northeastern
U.S., NMFS listed rainbow smelt as a species of concern in 2004 (NMFS 2007a).
510.5.7. River Herring
1. River herring collectively refers to Alewife (Alosa pseudoharengus) and Blueback
herring (Alosa aestivalis). Because of difficulties in distinguishing between alewife and
blueback herring, these two species are managed together under this collective term and
are discussed here together. Both species are designated as species of concern.
Life History and Habitat
2. Alewife are currently distributed from Newfoundland to North Carolina, whereas
blueback herring are distributed from Nova Scotia to Florida. Alewife reach lengths of
between 14 and 15 inches (36-38 cm) and live up to 10 years, whereas blueback herring
grow to approximately 15 inches (40 cm) and live 8 years. Both are small, anadromous
fish. Alewife initiate spawning when water temperatures reach 41 to 50° F (5-10 C°), and
are prolific, producing between 60,000 and 467,000 eggs each year. Blueback herring
spawn in slightly warmer water and therefore follow alewife spawning by 3 to 4 weeks;
egg production varies based on age and size. Both alewife and blueback herring feed on
plankton as well as small fish while at sea. Both alewife and blueback herring are
schooling fish while at sea and make seasonal migrations (Collette and Klein-MacPhee
2002).
Management
3. Alewife and blueback herring are managed together with shad, another anadromous fish,
by the Atlantic States Marine Fisheries Commission. Both species were historically the
target of both commercial and recreational fisheries, and in New England, landings
declined dramatically between the 1970s and the 1990s. According to NMFS, river
herring have declined due to a variety of factors including fishing pressure and mortality
due to bycatch, habitat degradation, and dams that impede spawning (NMFS 2009e).
Rhode Island and other adjacent states currently prohibit the harvest of river herring
(ASMFC 2007). NMFS (2009e) designated both alewife and blueback herring as species
of concern in 2006, citing a variety of demographic and genetic diversity concerns.
Currently, there are several restoration initiatives taking place in upper Narragansett Bay
that will restore fish passage and enhance depleted spawning populations of anadromous
species including river herring (RI Coastal Resources Management Council 2010). These
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initiatives may result in an increase of river herring in the Ocean SAMP area in future
years.
510.5.8. Sand Tiger Shark (Carcharias Taurus)
1. Sand tiger sharks can be found throughout the western Atlantic, and in southern New
England are common in shoal waters near Woods Hole and Nantucket, MA (Collette and
Klein-MacPhee 2002).
Life History and Habitat
2. Sand tiger sharks may grow up to 10.4 feet (318 cm) and live up to 17 years. Like many
sharks, sand tiger sharks bear live young, nourishing them in utero with egg yolk prior to
birth. Reproduction takes place every other year and a litter typically includes just one or
two pups (NMFS 2009f). Sand tiger sharks have been described as relatively sluggish
(Collette and Klein-MacPhee 2002). They are more active at night and are primarily
coastal. They usually live near the bottom. Sand tiger sharks are voracious predators and
feed on fish, small sharks and rays, squid, and some crustaceans (NMFS 2009f).
Management
3. Sand tiger sharks were historically harvested commercially in southern New England
during the early 20th century (Collette and Klein-MacPhee 2002), though they are more
commonly targeted in Japan for food. Increased exploitation in the 1980s and 1990s
resulted in notable abundance declines. Sand tiger sharks are managed by NMFS under
the Consolidated Atlantic Highly Migratory Species Fishery Management Plan, which
currently prohibits the landing of sand tiger shark for commercial and recreational
purposes, and by the Atlantic States Marine Fisheries Commission under the Interstate
Fishery Management Plan for Atlantic Coastal Sharks. According to NMFS, sand tiger
shark populations have declined because of fishing pressure and bycatch, because of their
low reproduction rates, and because of estuarine pollution. For these reasons the sand
tiger shark was listed as a species of concern throughout its entire range in 1997 (NMFS
2009f).
510.5.9. Thorny Skate (Amblyraja radiate)
1. Thorny skate is one of several skate species that occurs from Labrador to South Carolina.
They are more abundant in the Gulf of Maine and only infrequently found in shallow,
inshore areas.
Life History and Habitat
2. Thorny skate grow to lengths of over 39 inches (1 m) (NMFS 2009g) and live up to 20
years (Collette and Klein-MacPhee 2002). Thorny skate reproduce by depositing a
single, fertilized egg in a rectangular, thorned egg capsule approximately 2-4 inches (48
to 96 mm) long. Thorny skate feed on benthic fish and invertebrates. They appear to be
sedentary creatures with a preference for a range of bottom types and water temperatures
ranging from 29 to 57° F (-1.4 to 14° C) (Collette and Klein-MacPhee 2002).
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Management
3. Thorny skate are one of several skates historically harvested in New England. Skate
species are not specified in NMFS commercial fisheries landings data; unspecified skate
landings have increased markedly since the late 1970s/early 1980s. Northeast Fisheries
Science Center trawl survey data indicates that thorny skate biomass has declined since
the 1960s and is now historically low (NEFSC 2006a). The New England Fishery
Management Council manages thorny skate as part of the Northeast Skate Complex
Fishery Management Plan. At present the species is overfished and overfishing is
occurring. In addition to direct harvest by commercial fishermen, NMFS sites bycatch,
predation of skate embryos, and competition for prey resources as the reasons for thorny
skate’s decline. NMFS listed thorny skate as a species of concern in 2004 in response to
a series of demographic and genetic diversity concerns (NMFS 2009g).
510.6. Baseline Characterization
1. This section presents baseline data characterizing fisheries resources within and around
the Ocean SAMP area. The purpose of the baseline characterization is to provide baseline
information on the current state of fisheries resources in the area based on existing survey
data. It is not an assessment of individual fish stocks, nor is it an analysis of longer-term
trends in Rhode Island’s offshore fisheries resources. Ten years of fisheries-independent
bottom trawl survey data were used in this analysis as this provides enough data to
smooth out interannual variability while still allowing an assessment of the current state
of Ocean SAMP area fisheries resources. In addition, a ten-year period, rather than a
longer time period, was chosen for this analysis because the goal was to assess the
current, baseline conditions of fishery resources within the Ocean SAMP area, not to
analyze longer-term trends in abundance. This ten-year time period does not represent an
idealized state or a targeted abundance level; rather it is intended to provide current
abundance data in order to inform decision-making. For a more detailed discussion of
data sources, methods, and data products for the baseline characterization, see Bohaboy
et al. 2010, included in Appendix A. See Chapter 2, Ecology of the Ocean SAMP
Region, for discussion of the interactions of fisheries resources with other aspects of the
ecosystem, and for data on longer-term trends in stock abundance.
2. There is no one fisheries-independent survey or dataset that provides insight into the
abundance and biomass of finfish, shellfish, and crustacean species throughout the entire
Ocean SAMP area. Accordingly, data from four different bottom trawl surveys that are
regularly conducted in or around the Ocean SAMP area were aggregated and analyzed to
provide this baseline characterization. Data used in this analysis were obtained from the
RI Department of Environmental Management (RIDEM) trawl survey (1999-2008); the
URI Graduate School of Oceanography (GSO) trawl survey (1999-2008); the Northeast
Area Monitoring and Assessment Program (NEAMAP) trawl survey (2007-2008); and
the National Marine Fisheries Service (NMFS) trawl survey (1999-2008). Data included
in this analysis were collected at survey stations within a polygon delineated by the
following coordinates:
41° 30’ N, 071° 50.5’W
40° 50’ N, 071° 50.5’W
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41° 30’ N, 070° 50’W
40° 50’ N, 070° 50’W
Survey stations that occur adjacent to but just outside the Ocean SAMP area were
included in this analysis in order to allow for a comprehensive analysis of fisheries
resources in and around the planning area. See Figure 5.1 for a map showing the location
of each of the survey stations included in this analysis, and see Appendix A for further
discussion of data sources and methodology.
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Figure 5.1. Locations of survey stations used in baseline characterization.
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3. The RIDEM, GSO, NEAMAP, and NMFS bottom trawl surveys are all conducted for
research purposes and are also used to inform stock assessments and other fisheries
management decisions. The RIDEM survey is conducted in Rhode Island state waters but
does not include survey stations within the state waters surrounding Block Island. The
GSO survey has been run by URI since 1959, and is the longest continuous record of fish
and invertebrate relative abundance in Rhode Island.7 The NEAMAP survey is also
unique in that a fisherman conducts the survey, using gear designed by fishermen and
drawing upon advice from local fishermen about which of the randomly-selected survey
stations in a given area are towable.8 In all cases, the purpose of these surveys is to assess
the overall occurrence of fisheries resources in the area, not to compare relative
occurrence or abundance at specific sites.
4. Bottom trawl surveys, which employ the use of otter trawls, are used for this baseline
characterization because they provide the only consistent record of fish abundance.
However, while bottom trawl surveys are appropriate for sampling demersal and some
pelagic species, they may not accurately characterize the occurrence of some pelagics,
shellfish and crustaceans. Moreover, bottom trawl surveys do not sample untrawlable
bottom types of high habitat complexity, which may include moraines and other rocky
areas. For these reasons, this baseline characterization does not provide insight into all
habitats of importance as well as several recreational species of importance (see list
above). It should also be noted that site-specific surveys employing multiple gear types
will be required as part of the permitting process for future developments within the
Ocean SAMP area; see Section 560, Policies and Standards, for further discussion.
5. The baseline characterization focused on 29 finfish, shellfish, and crustacean species and
assessed species abundance and biomass. Baseline characterization species included the
above-mentioned commercially and recreationally targeted species, with the exception of
some pelagics (e.g. tunas) which are not adequately sampled in bottom trawl surveys.
This analysis also included several “Species of Concern” (see Section 510.5) which are
present in the Ocean SAMP area and adequately sampled through bottom trawl surveys.
Abundance and biomass for these species were assessed for the spring and fall seasons in
aggregate and for each individual species. Survey data were aggregated by calculating
the survey catch weight (biomass) for each survey by dividing the catch per tow (weight)
by the area of each tow. Survey biomass units are milligrams per square meter (mg / m2).
The purpose of these calculations was to allow for comparison between the surveys.
However, these calculations do not account for all differences between the surveys, and
results show that relative biomass estimates nonetheless vary significantly between the
surveys (Bohaboy et al. 2010). See Appendix A for further details on data sources and
methodology.
7 For further information on the URI GSO Fish Trawl Survey, see http://www.gso.uri.edu/fishtrawl/.
8 For further information on the NEAMAP Mid-Atlantic Nearshore Trawl Survey, see http://www.neamap.net/.
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Table 5.31.
Species assessed in the baseline characterization. See Bohaboy et al 2010, included in
Appendix A.
Common Name
Scientific Name
Alewife
Alosa pseudoharengus
American lobster
Homarus americanus
American shad
Alosa sapidissima
Atlantic cod
Gadus morhua
Atlantic herring
Clupea harengus
Atlantic mackerel
Scomber scombrus
Atlantic sea scallop
Placopectin magellanicus
Barndoor skate
Dipturus laevis
Black sea bass
Centropristis striata
Blueback herring
Alosa aestivalis
Bluefish
Pomatomus saltatrix
Butterfish
Peprilus triacanthus
Cusk
Brosme brosme
Dusky shark
Carcharhinus obscurus
Goosefish
Lophius americanus
Little skate
Leucoraja erinacea
Longfin squid
Loligo pealeii
Rainbow smelt
Osmerus mordax
Scup
Stenotomus chrysops
Silver hake
Merluccius bilinearis
Smooth dogfish
Mustelus canis
Spiny dogfish
Squalus acanthias
Striped bass
Morone saxatilis
Summer flounder
Paralichthys dentatus
Tautog
Tautoga onitis
Thorny skate
Amblyraja radiate
Winter flounder
Pseudopleuronectes americanus
Winter skate
Leucoraja ocellata
Yellowtail flounder
Limanda ferruginea
510.6.1. Analysis of Total Catch Biomass
1. Analysis of total catch biomass was conducted to determine the sources of variability in
the data by assessing the effects of season (fall or spring), survey (RIDEM, GSO,
NEAMAP, or NMFS), water depth, and part of the Ocean SAMP area (east or west).
Multiple-way analysis of variance based on natural log transformed data indicates that
season, survey, and depth are all significant factors affecting total survey biomass (actual
p-value < 0.001). Region, as defined by survey stations east or west of -71.38° (West)
longitude, does not have a significant effect on total catch biomass. As is illustrated by
Figure 5.2, total catch biomass is higher in the fall and lower in the spring. This
difference may be due to the fact that young of the year (YOY) are recruited to the
fishery in the fall and thus reflected in fall trawl surveys. Figure 5.2 also illustrates that
deep depth strata (60 to 90 ft and 90+ ft) have higher total catch biomass than shallow
depth strata (20 to 40 ft and 40 to 60 ft) (Bohaboy et al. 2010).
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Spring
Fall
0
20
40
60
80
Season
NMFS
DEM
GSO
NMP
0
20
40
60
80
Survey
20-40
40-60
60-90
90+
0
20
40
60
80
Depth (ft)
East
West
0
20
40
60
80
Region*
milligrams per square meter (mg/m2)
Total Biomass
Figure 5.2. Results of multi-way ANOVA of total biomass. (Bohaboy et al. 2010)
*Region defined as survey stations east or west of -71.38° (west) longitude. See Appendix A for data
sources and methods, including sample sizes for each analysis.
2. The spatial distribution of total catch biomass during the spring and fall seasons is shown
below in Figure 5.3 and Figure 5.4. A comparison of these figures indicates that there is a
depth/season interaction in the spatial distribution of total catch biomass. Figure 5.3
illustrates that in the spring, higher biomass is largely located inshore in shallower,
protected waters. By contrast, Figure 5.4 illustrates that in the fall, higher biomass is
distributed further offshore in deeper, open waters. It should be noted that these maps
reflect a synthesis of data from the four different fisheries-independent trawl surveys;
however, there are differences between the vessel types, gear types, and methods used in
these different surveys. It should also be noted that the absence of biomass, or relatively
low biomass, in a given area does not necessarily mean that there are no fish there.
Rather, it may mean that the area was not sampled through any of the survey programs.
See Appendix A for maps showing the spatial distribution of individual species biomass
and for further discussion of data sources and methodology.
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Figure 5.3. Aggregate fish biomass, 1999-2008, spring.
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Figure 5.4. Aggregate fish biomass, 1999-2008, fall.
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510.6.2. Analysis of Catch by Individual Species
1. Catch biomass data from the four trawl surveys were also used to assess the relative
biomass of key species for which data were available. Figure 5.5 below shows the
relative biomass of individual species within the study area based on a simple sum of
RIDEM, GSO, and NMFS survey data from 1999-2008. NEAMAP data were not
included in this figure as only two years of data are available. This figure illustrates that
in the fall surveys, little skate, scup, and longfin squid were among the species with the
highest relative biomass in the study area, whereas in the spring surveys, little skate,
scup, and winter flounder were among the species with the highest relative biomass in
the study area. Figures 5.6 to 5.9 below show the relative biomass of individual species
based on each seasonal survey. Note that all figures represent the relative biomass on a
logarithmic scale to allow for comparison between the figures (Bohaboy et al. 2010).
DEM/GSO/NMFS Total Biomass per Area
by Species, 1999-2008
0
0.001
0.01
0.1
1
10
100
Little skate
Scup
Longfin squid
Butterfish
Summer flounder
American lobster
Winter skate
Winter flounder
Silver hake
Bluefish
Black sea bass
Goosefish
Striped bass
Atlantic sea scallop
Yellow tail flounder
Alew ife
Tautog
Blueback Herring
Atlantic herring
Atlantic cod
Atlantic mackerel
American shad
mg per m2
Spring
Fall
Figure 5.5. Total biomass per area by species, 1999-2008. (Bohaboy et al. 2010).\
*Based on RIDEM, URI GSO, and NMFS trawl surveys
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DEM Biomass per Area by Species, 1999-2008
0
0.001
0.01
0.1
1
10
100
Little skate
Scup
Longfin squid
Butterfish
Summer flounder
American lobster
Winter skate
Winter flounder
Silver hake
Bluefish
Black sea bass
Goosefish
Striped bass
Atlantic sea scallop
Yellow tail flounder
Alew ife
Tautog
Blueback Herring
Atlantic herring
Atlantic cod
Atlantic mackerel
American shad
mg per m2
Spring
Fall
Figure 5.6. DEM trawl survey biomass per area by species. (Bohaboy et al. 2010)
GSO Biomass per Area by Species,1999-2008
0
0.001
0.01
0.1
1
10
100
Little skate
Scup
Longfin squid
Butterfish
Summer flounder
American lobster
Winter skate
Winter flounder
Silver hake
Bluefish
Black sea bass
Goosefish
Striped bass
Atlantic sea scallop
Yellow tail flounder
Alew ife
Tautog
Blueback Herring
Atlantic herring
Atlantic cod
Atlantic mackerel
American shad
mg per m2
Spring
Fall
Figure 5.7. GSO trawl survey biomass per area by species. (Bohaboy et al. 2010)
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NMFS Biomass per Area by Species, 1999-2008
0
0.001
0.01
0.1
1
10
100
Little skate
Scup
Longfin squid
Butterfish
Summer flounder
American lobster
Winter skate
Winter flounder
Silver hake
Bluefish
Black sea bass
Goosefish
Striped bass
Atlantic sea scallop
Yellow tail flounder
Alew ife
Tautog
Blueback Herring
Atlantic herring
Atlantic cod
Atlantic mackerel
American shad
mg per m2
Spring
Fall
Figure 5.8. NMFS trawl survey biomass per area by species. (Bohaboy et al. 2010)
NEAMAP Biomass per Area by Species,
Fall 2007/2008 and Spring 2008
0
0.001
0.01
0.1
1
10
100
Little skate
Scup
Longfin squid
Butterfish
Summer flounder
American lobster
Winter skate
Winter flounder
Silver hake
Bluefish
Black sea bass
Goosefish
Striped bass
Atlantic sea scallop
Yellow tail flounder
Alew ife
Tautog
Blueback Herring
Atlantic herring
Atlantic cod
Atlantic mackerel
American shad
mg per m2
Spring
Fall
Figure 5.9. NEAMAP trawl survey biomass per area by species. (Bohaboy et al. 2010)
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2. Individual species catch biomass data also provide insight into trends in biomass over the
past decade. Data from the DEM, GSO, and NMFS trawl surveys were used to assess
trends in biomass for the Ocean SAMP area from 1999 to 2008; spring and fall trends
figures for each of the key species for which data were available are included in
Appendix A. NEAMAP data were not used in these figures as only two years of data
were available.
3. Multivariate analyses identified 17 species that effectively control the demersal fish and
invertebrate community composition within the Ocean SAMP area (see Figure 5.10
below). Although these species may not be the most abundant within the Ocean SAMP
area, they are of immense ecological importance to the stability and resiliency of the
local marine community. When attempting to predict the effects of development and
exploitation on the demersal fish community within the Ocean SAMP area, it is essential
to consider these community-shaping species. As illustrated by this figure, many of these
species vary in abundance from fall to spring. Such seasonal community dynamics
should also be considered when planning offshore construction and directed exploitation
(Bohaboy et al. 2010).
Figure 5.10. Spring and fall biomass of species identified as a driver of demersal fish and invertebrate
community composition (Primer 6.0, BVStep, R=0.940). (Bohaboy et al. 2010)
4. The spatial distribution of individual species catch biomass during the spring and fall
seasons is shown in a series of maps that are included in Appendix A. Maps are included
for all of the species identified in Figure 5.10, as well as the remaining species of
commercial and recreational importance for which bottom trawl survey data were
available.
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Section 520. Fish Habitat in the Ocean SAMP area
520.1. Benthic Habitat
1. Fish populations in the Ocean SAMP area and elsewhere require access to suitable
habitats at all stages of the life cycle in order to thrive. Habitat requirements vary widely
by species. Suitable habitat for a given species may include specific chemical and
physical properties of the water column as well as specific geological or biological
bottom characteristics. For an extensive discussion of habitat in the Ocean SAMP area,
as well as other ecosystem characteristics, see Chapter 2, Ecology of the Ocean SAMP
Region.
2. This section focuses on the current status of fish habitat in the Ocean SAMP area.
Potential impacts to habitat from existing activities are discussed below in Section 550. It
should be noted that future uses of the Ocean SAMP area may result in habitat
disturbances. Conversely, future uses of the Ocean SAMP area may result in habitat
enhancements through the creation of artificial reefs or other factors. See Chapter 8,
Renewable Energy and Other Offshore Development for discussion of the potential
effects of renewable energy on fish habitat, and Chapter 9, Other Future Uses for
discussion of artificial reefs and other potential future uses of the Ocean SAMP area.
3. Very little mapping of geological and biological habitats has been done to date in the
Ocean SAMP area. At the time of this writing, URI Graduate School of Oceanography
researchers are conducting research on benthic habitat and have mapped approximately
15% of the total Ocean SAMP area. Future efforts by these researchers and by the
NOAA hydrographic mapping program will result in approximately 40% of the area
being mapped by 2011. This work will provide maps of geological and biological
habitats, including fish habitat, for those areas being studied (J. King and J. Collie pers.
comm.). Results of this study are forthcoming in 2010 and will be incorporated into
subsequent revisions of the Ocean SAMP document. Preliminary results are summarized
in Chapter 2, Ecology of the SAMP Region. A technical report detailing these
preliminary results (Malek et al. 2010) may be found in the Ocean SAMP Appendices.
520.2 Habitat Requirements for Species of Importance
1. As noted above, habitat requirements vary widely by species. Table 5.32 below is a
summary of the habitat requirements for the commercial and recreational species of
importance found within the Ocean SAMP area, summarized from Section 510.3; this
table also includes a column summarizing the presence of designated Essential Fish
Habitat (EFH) in the area. See Section 520.3 below for further discussion. For more
information on specific habitat preferences, please refer to the individual species
descriptions and tables in Section 510.3.
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Table 5.32. Habitat requirements for species of importance found within the Ocean SAMP area.
This table is a summary of Tables 5.3-5.28 included above in the individual species descriptions; for
references, see those individual tables.
Species
Life
Stage
Pelagic
Rocky
Cobble
Sand
Mud
Clay
Gravel
Boulder
Algae/
Vege-
tation
Shell
fragments/
shellfish
beds
Man-
made
structures
/wrecks
EFH Des-
ignated in
Ocean
SAMP
Area
Eggs
X
N/A
Larvae
X
Juveniles
X
American
Lobster
Adults
X
X
X
Juveniles X
N/A
Atlantic
bonito
Adults
X
Eggs
X
X
Larvae
X
X
Juveniles
X
X
X
Atlantic
cod
Adults
X
X
X
Eggs
X
X
X
X
X
X
X
Larvae
X
X
Juveniles X
X
Atlantic
herring
Adults
X
X
X
Eggs
X
X
Larvae
X
X
Juveniles X
X
Atlantic
mackerel
Adults
X
X
Eggs
X
Larvae
X
X
X
Juveniles
X
X
X
X
X
Atlantic
sea
scallop
Adults
X
X
X
X
X
Eggs
X
Larvae
X
X
Juveniles
X
X
X
X
X
X
Black sea
bass
Adults
X
X
X
X
X
X
Bluefish
Eggs
X
X
Larvae
X
X
Juveniles X
X
X
X
X
X
Adults
X
X
Butterfish
Eggs
X
X
Larvae
X
X
Juveniles
X
X
Adults
X
X
X
Juveniles X
N/A
False
albacore
Adults
X
Monkfish
Eggs
X
X
Larvae
X
X
Juveniles
X
X
X
X
X
X
Adults
X
X
X
X
X
X
Eggs
X
X
X
X
X
X
Larvae
X
Juveniles X
X
Loligo
squid
Adults
X
X
X
X
Eggs
X
Larvae
X
Juveniles X
X
X
X
X
Menhaden
Adults
X
X
X
X
N/A
Scup
Eggs
X
X
Larvae
X
X
Juveniles
X
X
X
X
X
Adults
X
X
X
X
X
X
X
Juveniles X
Sharks
(all)
Adults
X
N/A
Eggs
X
X
Larvae
X
X
Juveniles X
X
X
X
Silver
hake
Adults
X
X
X
X
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Eggs
X
Juveniles
X
X
X
X
Skate,
little
Adults
X
X
X
X
Juveniles
X
X
X
Skate,
winter
Adults
X
X
X
Juveniles X
Spiny
dogfish
Adults
X
X
X
N/A
Eggs
X
Larvae
X
X
X
Juveniles
X
X
X
Striped
bass
Adults
X
X
X
X
N/A
Eggs
X
X
Larvae
X
X
X
Juveniles
X
X
X
X
Summer
flounder
Adults
X
X
X
X
X
Tautog
Eggs
X
Larvae
X
Juveniles
X
X
X
X
X
Adults
X
X
X
X
N/A
Juveniles X
Tunas
(all)
Adults
X
N/A
Eggs
X
X
X
X
Larvae
X
X
X
Juveniles
X
X
X
Winter
flounder
Adults
X
X
X
X
X
X
X
Eggs
X
X
Larvae
X
X
Juveniles
X
X
X
Yellowtail
flounder
Adults
X
X
X
520.3 Essential Fish Habitat
1. Under the Magnuson-Stevens Act, Essential Fish Habitat (EFH) is defined as “those waters
and substrate necessary to fish for spawning, breeding, feeding, or growth to maturity.” EFH
is designated by the respective regional fishery management councils through their fishery
management plans. EFH designation requires NMFS and federal agencies to work to protect
these areas from actions which may have an adverse effect on EFH (NMFS n.d.). The New
England Fishery Management Council is in the process of developing an Omnibus Habitat
Amendment that will address the effects of fishing on Essential Fish habitat.
2. Within the Ocean SAMP area, EFH has been designated for 24 finfish, shellfish, and
crustacean species for at least part of their life cycle (see Table 5.33 below). Figure 5.11
below shows the total number of EFH species per ten minute square; Figures 5.12 to 5.15
below show the number of EFH species per ten minute square by life stage.
Table 5.33. Species for which Essential Fish Habitat has been designated within the Ocean SAMP area.
(NMFS Office of Habitat Conservation, 2010)
American plaice
Scup
Atlantic cod
Silver hake
Atlantic herring
Skate, little
Atlantic mackerel
Skate, winter
Atlantic sea scallop
Spiny dogfish
Black sea bass
Squid, Illex
Bluefish
Squid, Loligo
Butterfish
Surf clams
Haddock
Summer flounder
Monkfish
Windowpane flounder
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Ocean pout
Winter flounder
Ocean quahog
Witch flounder
Red hake
Yellowtail flounder
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Figure 5.11. Number of species per ten minute square with Essential Fish Habitat, all life stages. (Data: NMFS; Map prepared by RIDEM Div. Fish and
Wildlife, 2010)
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Figure 5.12. Number of species per ten minute square with Essential Fish Habitat, egg life stage. (Data: NMFS; Map prepared by RIDEM Div. Fish and
Wildlife, 2010)
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Figure 5.13. Number of species per ten minute square with Essential Fish Habitat, larval life stage. (Data: NMFS; Map prepared by RIDEM Div. Fish and
Wildlife, 2010)
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Figure 5.14. Number of species per ten minute square with Essential Fish Habitat, juvenile life stage. (Data: NMFS; Map prepared by RIDEM Div. Fish
and Wildlife, 2010)
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Figure 5.15. Number of species per ten minute square with Essential Fish Habitat, adult life stage. (Data: NMFS; Map prepared by RIDEM Div. Fish and
Wildlife, 2010)
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3. Under the Magnuson-Stevens Act, federal agencies must consult with NMFS on actions
that adversely affect EFH. Part of an EFH consultation is an EFH assessment, which is a
site- and project-specific analysis of the potential impacts of an action on EFH.
520.4. Critical Habitat
1. Under the Endangered Species Act, Critical Habitat is designated for species listed under
the Act as threatened or endangered. The ESA describes Critical Habitat as those areas
that are “essential to the conservation of the species and which may require special
management considerations or protection.” According to the NOAA Northeast Regional
Office Protected Resources Division, there is no Critical Habitat for any listed finfish
species within the Ocean SAMP area (Crocker, pers. comm. a.).
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Section 530. Commercial and Recreational Fisheries in the Ocean SAMP Area
530.1. History of Fisheries in Rhode Island
530.1.1. Commercial Fishing History
1. The commercial fisheries of Newport and Sakonnet Point have origins dating back to the
17th century (Hall-Arber et al. 2001). Colonial fishermen in Rhode Island used a hook
and line and fished from a small skiff, or set seine nets along the shore. The small fish
caught with seines were used primarily as manure in the fields (Olsen et al. 1980).
Seining usually involved leaving a net in the water for an hour or so, and returning to pull
up the net and whatever it had caught. Poggie and Gersuny (1974) describe the fishing
gangs in South Kingstown who would have fish houses along the beach equipped with
bunks, where they would stay while fishing for striped bass. Each fishing gang typically
used two boats and a seine.
2. The historically important food species of fish in Rhode Island have been striped bass,
scup, tautog, bluefish, and mackerel (Sedgwick et al. 1980). During the mid-1800s, the
use of staked and floating fish traps, set close to shore, came into prominence as a fishing
technique, eclipsing the hook and line method. This new method of fishing was much
more efficient (Olsen et al. 1980). At the time, traditional hook and line fishermen
claimed that the waters of Rhode Island were being overfished by these new
technologies. In 1870, the Rhode Island General Assembly appointed a special
committee to investigate these claims (Poggie and Gersuny 1974). By 1910 there were
400 fish traps in use throughout Rhode Island. Eventually, because they were so
numerous, the state placed restrictions on where and when they could be used (Olsen et
al. 1980).
3. Fishermen also seined for menhaden using larger nets, usually requiring a more
substantial operation with four men rowing the boat, two men to throw the net overboard,
and about sixteen men on shore to haul the net ashore. Typically, neighbors would assist
in the process in exchange for a share of the catch. Menhaden were generally used for
rendering fertilizer and fish oil rather than food, and as many as 100,000 were sometimes
taken in a single catch (Poggie and Gersuny 1974). Menhaden became a highly important
industrial fishery in Rhode Island and throughout New England in the late 1800s and
early 1900s. In 1889, there were a reported 127 million pounds of fish landed in Rhode
Island, of which 89 percent were menhaden (Olsen and Stevenson, 1975). Menhaden
plants, which rendered the fish for oil, were common along the New England coastline
around the turn of the century. Scup and alewives were also important species to
commercial fisheries in this period (Poggie and Pollnac, eds. 1981).
4. The development of the fishing industry coincided with the development of markets for
fish and with the ability to store and transport fish. Around the turn of the last century,
fish could be shipped by steamship from Newport to New York, or via railroad. There is
evidence that ice was used in keeping fish as early as 1900, but its early use was limited
because of cost (Poggie and Gersuny 1974). Other methods of shipping fish included
boxing them or placing them in barrels (Sedgwick et al. 1980).
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5. During the 1920s and 1930s, menhaden began to disappear off the coast of New England
as stocks were overfished, and many of the menhaden plants were forced to close.
Fishermen were pushed to pursue other species (Poggie and Pollnac, eds. 1981). In the
1930s, the first otter trawls were used off Rhode Island (Olsen and Stevenson 1975).
Marine diesel engines were also introduced around this time, allowing fishermen to
travel further offshore in pursuit of fish (Poggie and Pollnac, eds. 1981). Trawling
quickly became the dominant method of fishing, and trap fishermen soon began
criticizing trawlers for a decline in stocks. Whiting (silver hake) and red hake, both used
for industrial purposes, usually in the form of fertilizer or protein, were the two species
initially targeted by otter trawls (Poggie and Pollnac, eds. 1981). As trawling became
more commonplace, the species caught as well as people’s preferences for food fish both
changed, and flounder, which had previously been considered “trash” fish, eclipsed scup,
bluefish, and mackerel in the marketplace (Sedgwick et al. 1980). See Figure 5.16 for
offshore areas used by trawlers during the 1970s.
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Figure 5.16. Historic trawling areas of the 1970s.
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6. During the 1960s, significant stocks of lobsters that had not previously been fished were
discovered offshore, providing a large boost to landings and value in the state’s lobster
fishery (Sedgwick et al. 1980). Around this time, traps replaced trawling as the dominant
method for catching lobsters offshore, and this also significantly boosted lobster landings
and revenues (Poggie and Pollnac, eds. 1981).
7. As in other states around the country, the presence of foreign fishing fleets was a
contentious issue in Rhode Island in the 1960s through the mid-1970s, until the passage
of the Magnuson Stevens Fishery Conservation and Management Act in 1976, which
declared a 200-mile limit on U.S. waters. Rhode Island offshore fisheries continued to
grow even during the time of massive fishing efforts by foreign fleets, as some of the
offshore stocks were not heavily exploited by foreign fleets, and were thus targeted by
Rhode Island vessels. A significant period of development in fisheries followed the
passage of the Act, in which Rhode Island fishermen, more so than other New England
fishermen, diversified their targeted species to include butterfish, whiting (silver hake),
and squid, based both on the abundance of these species in Rhode Island waters
compared with northern New England, where their geographic range does not extend,
and also on a willingness of Rhode Island fishermen to target non-traditional species
(Sedgwick et al. 1980). This led to rapid expansion of Rhode Island fisheries in the late
1970s and early 1980s. In 1979, there were a record 264 offshore vessels landing at
Rhode Island ports, although some of these vessels were home ported elsewhere. As the
number of vessels grew in this period, so did vessel length, tonnage, and horsepower, and
the traditional wooden eastern rigged side trawler was replaced by new steel-hulled stern
trawlers (Sedgwick et al. 1980).
8. Rhode Island’s important squid fishery began in the late 1800s as a bait fishery, and a
market for human consumption developed during the 1960s. Whereas longfin squid have
been harvested since the late 1800s, harvesting of shortfin (illex) squid as a bait fishery
began somewhat more recently. From the late 1960s through early 1980s, longfin squid
were heavily exploited in Rhode Island waters by foreign fishing fleets. After the
departure of foreign vessels from U.S. waters, Rhode Island vessels were among the first
to target squid in large numbers; Rhode Island commercial landings for longfin squid
increased by an order of magnitude from 1981 through 1992 (DeAlteris et al. 2000).
9. During the 1980s, the commercial fishing industry in Rhode Island was growing,
increasing by 24 percent in total landings from 1980 through 1987, while landings in the
other New England states declined by 37 percent. This increase was due in part to an
increase in fish consumption nationwide, to the increased harvesting of what at the time
were underutilized species (such as squid, butterfish, and silver hake), and also to a
significant increase in international exports from Rhode Island, particularly to Japan.
This growth was also aided by public investment into the fishing industry during the late
1970s and 1980s, including the development of piers at both Newport and Galilee
(Intergovernmental Policy Analysis Program, University of Rhode Island, 1989).
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530.1.2. Recreational Fishing History
1. Recreational fishing, also known as sport fishing, also has a long and important history in
Rhode Island. However, as with many other types of recreation, there is very little
documentation of recreational fishing history, both in Rhode Island and throughout the
U.S. In the late 19th-century, recreational boating became a popular pastime, and Newport
and other Rhode Island coastal communities became destinations for wealthy people
seeking leisure time and recreational activities. Coastal recreation and tourism activities,
including boating and beach-going, became increasingly popular with the emergent
middle class during the early- to mid-20th century. Recreational fishing also emerged as a
popular activity during this time.
2. Rhode Island’s many fishing clubs and organizations are a testament to the presence of
recreational fishing within the state’s history. The Narragansett Salt Water Fishing Club,
for example, has been in existence since 1936, and the club had as many as 800 members
in the 1940s and 50s. Historically, there were tuna clubs in coastal communities such as
Block Island, where the Atlantic Tuna Club had a club house in 1915 (Allen 2010). The
RI Party and Charter Boat Association was established by 15 party and charter boat
operators in 1962 in order to promote their industry; today, membership has grown to 70
members from throughout the state with vessels ranging in size from 18 to 100 feet long
(Bellavance, pers. comm.). The RI Saltwater Anglers Association was established more
recently, in 1999, as a forum and advocacy organization for recreational fishermen, and
currently has approximately 1,800 members (Hittinger, pers. comm. a).
3. Rhode Island has a long history of recreational fishing tournaments, many of which are
focused on species found in the Ocean SAMP area. The Atlantic Tuna Tournament,
alternately known as the Point Judith Tuna Tournament, is one of the better known of
these tournaments. This tournament began in the 1940s (Conley 1986) and became
especially popular in the 1950s and 1960s, drawing large crowds to Galilee. Galilee was
known as the Tuna Capital of the World until the tournament was moved to Gloucester in
1973 (Olsen and Stevenson 1975). Other large recreational fishing tournaments described
in a 1986 history of Rhode Island include the Rhode Island Tuna Tournament, the Point
Judith Masters Invitational, the Snug Harbor Shark Tourney, the Block Island Bluefish
Tournament, and the Block Island Striper Tournament (Conley 1986).
4. Recreational fishing in Rhode Island has also expanded in recent years through the
growth of the party and charter boat industry. RI Department of Environmental
Management licensing data indicates that 240 party and charter boats are currently
licensed; this is more than twice the number than were licensed in 1999 when the
licensing program first took effect (RIDEM 2010b).
530.2. Rhode Island’s Commercial and Recreational Fishing Ports
1. Rhode Island today has two major commercial fishing ports, Point Judith and Newport,
as well as several smaller fishing ports used by both commercial and recreational
fishermen. These ports have seen significant changes over the years, as the fishing
industry has given way to tourism and other waterfront development. However, Rhode
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Island’s ports still serve as the physical and social nexus of fishing activity within the
state, and have an important place in the state’s history and culture.
2. Rhode Island’s commercial fishing ports serve commercial fishermen and fishing vessels
both from within the state of Rhode Island and from other states along the East Coast.
The nature of fishing regulations and markets is such that at various times of the year,
fishermen from as far away as North Carolina and Florida may be fishing in the Ocean
SAMP area, and may make use of the infrastructure present in the state to unload and sell
their catch. Likewise, Rhode Island fishermen may land their catch in other states at
times.
3. Because of the importance of recreational fishing to Rhode Island, recreational
fishermen, and boats used either occasionally or frequently for recreational fishing, can
be found in every port and harbor in the state. Point Judith and Newport, critical to the
state’s commercial fishing industries, also host much of the state’s recreational fishing
activity, particularly for vessels fishing within the Ocean SAMP area.
530.2.1. Point Judith/Galilee
1. Commercial fishing did not become a prominent industry at Point Judith until the 1930s.
During the 17th and most of the 18th centuries, farming was the primary activity in the
South Kingstown/Narragansett area (Narragansett was part of the town of South
Kingstown until splitting off in 1888). A textile industry developed in 1802, and was a
prominent industry here throughout the 19th century (Poggie and Gersuny 1974).
2. The development of the Point Judith commercial fishing industry coincided with the
development of the Harbor of Refuge. Between 1892 and 1915, the US Army Corps of
Engineers built three breakwaters at Point Judith to create the Harbor of Refuge (Olsen
and Stevenson 1975). Previously, Point Judith had presented a hazard to navigation
between Boston and New York, and the shifting sands of the pond had made it
impossible for use as a harbor. In 1934 and 1935, the state and the Public Works
Administration built two state piers and dredged a 35-acre anchorage basin – these
improvements allowed the commercial fishing industry to prosper here. Landings of
commercial fish at Point Judith grew exponentially from 300 tons in 1895 to 3,000 tons
in 1935, and then from 17,000 tons in 1945 to 30,000 tons in 1970 (Poggie and Gersuny
1974). The fishery during the 1950s was primarily an industrial fishery, largely for
whiting and red hake used as industrial feeds. This fishery had a rapid decline after
peaking in 1956, but other fisheries continued to be robust (Olsen and Stevenson 1975).
3. One major force in the development of the commercial fishing industry at Point Judith
was the creation of a cooperative. The Point Judith Fishermen’s Cooperative was
founded in 1948 by returning World War II veterans, and served as a marketing
cooperative for local fishermen, rather than as a fishing cooperative. At its start, it had 65
members and 20 fishing vessels (Poggie and Gersuny 1974). The coop provided its
members with organized marketing and with lumpers (fish handlers). They provided low-
cost insurance and unemployment compensation to members. The coop also had a store
where they sold equipment and supplies such as line, boots, gloves, and replacement
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parts, saving the coop members valuable time and money by not having to go elsewhere.
The coop also provided fuel and ice. By 1973, the coop had 129 members and employed
82 people. There were approximately 120 trawlers and lobster boats landing regularly at
the coop, and most of the fish was sold to Fulton Fish Market in New York (Olsen and
Stevenson 1975).
4. During the 1970s, as commercial fisheries expanded due to the creation of the 200 mile
limit, membership in the coop increased to the point where a moratorium was placed on
membership. In the 1980s, the coop increased its processing capacity by moving into a
larger building. During the moratorium, other companies developed to fill this gap, and
after its expansion there were few incentives to join the coop. The combination of
increased competition and growing operating costs (which were not accompanied by
growth in membership) contributed to the coop’s ultimate demise, and it shut its doors in
1994 (Griffith and Dyer 1996). Declining fish stocks and low prices also contributed to
the coop’s closure. The coop exists today as an independent fish marketing organization
(Clay et al. 2008).
5. Point Judith did not become a significant commercial fishing port until the 1930s, so it
lacks the long tradition of fishing of some other New England towns, including Newport.
Many of the fishermen do not come from fishing families with a long fishing history, but
became fishermen during the 1960s or 1970s as the industry was expanding. However,
many of the fishermen also have last names found in the 1774 census for South
Kingstown, indicating that many of the fishermen are from families who have lived in
the area for generations (Poggie and Gersuny 1974). Most of the commercial fishermen
who dock their vessels here live within a 20-mile radius of Point Judith, but not in the
immediate vicinity of the port, because of a lack of housing around Point Judith.
However, there is still a distinct community of fishermen, and culture of commercial
fishing, in Point Judith (Hall-Arber et al. 2001).
6. Today Point Judith is the center of the Rhode Island commercial fishing industry. The
vast majority of vessels docked at Point Judith use the port on a full-time basis, rather
than being transient among multiple ports. Most of Point Judith’s fishermen land there
throughout most of the year, although they frequently change targeted fisheries several
times throughout the year (Sedgwick et al. 1980).
7. Point Judith has sufficient infrastructure to support its commercial fishing industry, as
well as to provide shoreside services to fishermen around the state. There are a number of
docks, processing facilities, and dealers, and a commercial bait dealer to serve trap
fishermen (Clay et al. 2008). The Division of Coastal Resources of the Rhode Island
Department of Environmental Management is responsible for the development and
management of the port of Galilee. There are over 230 commercial fishing vessels,
including charter fishing boats, berthed in Galilee (RIDEM Division of Coastal
Resources n.d.).
8. The largest fish processors in Point Judith are the Town Dock Company and the Point
Judith Fishermen’s Company. Town Dock came to Point Judith in 1980 and is now one
of the largest seafood processing companies in Rhode Island. Its facility supports
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unloading, processing, and freezing facilities under one roof and services over half of the
trawlers based out of Point Judith (approximately 30 full-time deep sea fishing trawlers),
as well as a large day-boat fleet. They handle and process species including squid, scup,
and butterfish (Clay et al. 2008).
9. The Point Judith Fishermen’s Company, which employs approximately fifteen people at
its plant, processes squid which are sold wholesale at the Hunts Point Market in New
York. Handrigan’s is another unloading facility located in Point Judith. Several smaller
processors located in the Point Judith area include: Deep Sea Fish of RI, Ocean State
Lobster Co., Narragansett Bay Lobster Co., Fox Seafood, South Pier Fish Company, and
Osprey Seafood (also known as the Black Point Fish Trap Company) (Clay et al. 2008).
10. Trawlworks, Inc. in Narragansett is a manufacturer, supplier and distributor of marine
hardware and rigging supplies for industrial, institutional, and commercial fishing for
both mid-water and bottom use. The corporation was formed in 1980. Superior Trawl is
also located in Narragansett, and builds fishing gear sold throughout New England and
the Mid-Atlantic. The Bait Company sells bait to local lobstermen (Clay et al. 2008).
11. The majority of commercial vessels docked at Point Judith are bottom trawlers, and most
of these are between 45 and 75 feet in length. There are a few larger boats (70’ and
longer) which fish primarily for squid, herring, and whiting (silver hake), while many of
the medium sized boats target a mix of pelagic and groundfish species. Typically, the
smaller vessels have 1-2 person crews, while the larger boats may have a crew of four or
five. Generally, fishermen in Point Judith are flexible, and target whatever species are
available and marketable. Fishermen in Point Judith have the advantage of being close to
fish stocks, and of being able to switch between traditionally mid-Atlantic stocks such as
butterfish as well as traditionally northern fisheries such as the groundfish species
complex, which includes bottom-dwelling fish such as cod, haddock, and flounders.
Squid are usually caught year round, with the bulk of squid fishing done in May; herring
are caught December to April, mackerel are caught from March through May, and both
whiting and scup are caught year-round. Groundfishing boats fish both inshore and
offshore depending on the season, targeting traditional groundfish species offshore, and
yellowtail, winter, and summer flounder closer to shore. There are also a number of
lobster boats located in Point Judith, including both inshore and offshore lobster boats
(Hall-Arber et al. 2001). Much of the fish landed at Point Judith ends up either at the
Hunts Point Fish Market in New York or the Boston Fish Exchange. Fish product from
Point Judith is usually considered to be of high quality, and fetches a good price. Most of
Rhode Island’s fish exports are made up of squid and lobster (Hall-Arber et al. 2001).
12. Today Point Judith is still a major commercial fishing port. In 2009, there were 179
vessels with federal permits home ported in the Point Judith area (NMFS 2010e). The
most valuable species landed here were squid, butterfish, and mackerel, followed by
lobster. In 2008, it was ranked 17th among U.S. fish ports for total value of landings in
the United States, and 21st for weight (NMFS 2009a).
13. Point Judith is also a significant recreational fishing port. The majority of charter boats in
the state are based at Point Judith or in the port of Galilee, and all of the state’s party
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boats are found here. By one count, between 2001-2005, 66 different charter and party
boats made a total of 7,709 trips out of Point Judith, carrying almost 100,000 anglers
(Clay et al. 2008). The shores around Point Judith Pond are filled with marinas and
private docks, supporting a large number of recreational boats, a majority of which will
spend some time fishing within the Ocean SAMP area. Snug Harbor, across the pond
from Point Judith and Galilee, is home to numerous recreational fishing boats and hosts
several fishing tournaments.
14. Commercial and recreational fisheries are presently competing for space in Point Judith.
While the commercial fishing presence has diminished in Point Judith, as it has done
elsewhere around the state, recreational and for-hire fishing has expanded as part of the
state’s growing recreation and tourism economy. Many of the former gathering spots for
fishermen have been converted to ice cream shops and seafood restaurants. The
commercial fishing infrastructure cannot be further expanded because of competition
from the recreational boating sector (Hall-Arber et al. 2001). However, because of the
significant economic value of both recreational and commercial fishing in Point Judith,
and the cultural importance of both commercial and recreational fishing to this area,
commercial fishing is likely to retain a stronghold in Point Judith alongside a thriving
recreational fishing industry.
15. Point Judith has a Blessing of the Fleet celebration for the fishing fleet, featuring food,
games, parades, and other festivities. Traditionally, visitors would get to tour a
commercial fishing vessel and participate in the parade. However, the fishermen’s
insurance companies refused to cover the liability of any non-fisher who might be injured
on one of the vessels, and much of the commercial fleet had to stop participating in the
event (Griffith and Dyer 1996). The Blessing of the Fleet still takes place today, and
features a road race and seafood festival, but primarily involves recreational vessels. This
event has shifted away from a tradition of cultural importance for fishermen toward a
tourism-oriented event (Hall-Arber et al. 2001).
530.2.2. Newport
1. Newport’s history and cultural traditions are strongly tied to tourism and recreational
boating, and commercial fishing has also always had a presence here (Hall-Arber et al.
2001). Newport has one of the best natural harbors in the Northeast (Olsen and
Stevenson 1975). Although not much historical information is available on fishing during
Newport’s early history, it is a safe assumption that fishing played a vital role in
Newport’s economy in the early days when the city was first settled by Europeans
(Poggie and Pollnac, eds. 1981). Before the port of Galilee was developed, Newport was
the center of both shipping and fishing in Rhode Island. During the 1870s, there were
four industrial fish processing plants on Aquidneck Island processing menhaden,
mackerel, herring, and scup as agricultural fertilizers (Sedgwick et al. 1980). Commercial
fishing declined in prominence here after World War II, just as the Naval Base was
gaining in size and importance to the economy.
2. Newport was Rhode Island’s principal commercial fishing port in the 1930s but was
surpassed by Point Judith when its industrial fishery blossomed in the late 1940s and 50s.
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Some suggested factors in the decline of commercial fishing in Newport at that time
include the growth of recreational boating and tourism, and commercial fishermen being
enticed to New Bedford and Point Judith by the increase in services and infrastructure in
those ports (Poggie and Pollnac, eds. 1981). During the 1960s, Newport again became an
important port for trawlers from New Bedford (Olsen and Stevenson 1975). At this time,
many of the trawlers fishing in New Bedford and other ports, including many New Jersey
vessels, were dissatisfied with the dealers in these locations, and were enticed to Newport
by the dealers there (Poggie and Pollnac, eds. 1981). Olsen and Stevenson noted of
Newport in 1975 that the vessels landing here were on average larger than those landing
in Point Judith, making longer trips out to Georges Bank as opposed to shorter trips
closer to home. Newport was still the dominant commercial fishing port in Rhode Island
until around 1973 (Hall-Arber et al. 2001), but fishing here has declined considerably
since that time. During the 1970s, Newport’s waterfront underwent a dramatic
transformation as recreational boating, tourism, and residential development out-
competed commercial fishing for use of much of the city’s waterfront. There have been
no new commercial fishing-related businesses coming into the fishery in Newport for
close to thirty years. This has been the result of increasing property values, restricting
fishing-related businesses from opening, and increased competition for dock space with
recreational vessels (Hall-Arber et al. 2001).
3. Traditionally, a number of transient commercial vessels from New Bedford and other
ports have landed in Newport. These are usually long-trip boats fishing for scallops or
groundfish on Georges Bank that come to Newport to sell to one of the fish buyers here.
There are also a number of lobster boats that fish out of Newport. The Division of
Coastal Resources of the Rhode Island DEM is responsible for managing and
maintaining State Pier 9, the only state-owned commercial fishing facility in Newport.
The pier provides dockage for approximately 60 full-time commercial fishing vessels
(RIDEM Division of Coastal Resources n.d.), the majority of which are lobster boats
(Clay et al. 2008).
4. Newport has the infrastructure and services to support its commercial fishing fleet, but
has been losing fishing-related business in recent years, and at present commercial
fishermen must go to New Bedford or Point Judith for most fishing supplies. The city has
several seafood wholesalers and retailers. The most significant of these include: Omega
Sea, which markets scallops and coldwater shrimp; Aquidneck Lobster, a large lobster
wholesaler; and Parascandolo and Sons, which buys finfish. Other commercial fishing-
related businesses here include International Marine Industries, Long Wharf Seafood,
and Neptune Trading Group. Parascandolo and Sons maintains a private dock, primarily
used by the multispecies groundfish fleet who land fish here, but they also have a
substantial number of vessels landing squid here. Parascandolo and Sons requires a large
volume in order to be able to maintain their business (Clay et al. 2008).
5. In 2009, there were 41 commercial vessels with federal licenses listing Newport as their
home port (NMFS 2010e). Newport was ranked 75th among U.S. fish ports for landings
value in 2008, and 60th by weight (NMFS 2009a). In recent years, scallops and lobster
have been among the most valuable commercial species landed in Newport (Clay et al.
2008).
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6. Recreational fishing is an important activity in Newport because of the large number of
recreational boats located here.9 The harbor’s location means that recreational boats can
easily access the Ocean SAMP area. There are also several charter boats located in
Newport harbor.
7. Newport also has an annual Blessing of the Fleet that takes place each December as part
of the city’s Christmas celebrations, where both recreational and commercial vessels are
decorated for a parade around the harbor (Clay et al. 2008).
530.2.3. Sakonnet Point
1. Sakonnet Point in Little Compton is a considerably smaller port than either Point Judith
or Newport, but fishermen here also fish within the Ocean SAMP area. Commercial
fishing is considered to be one of the most important economic activities in Little
Compton. Most fishermen based in Sakonnet Point are combination lobster-gillnet
fishermen (Hall-Arber et al. 2001). There are a number of fish traps outside of Sakonnet
Harbor and at the mouth of the Sakonnet River, many currently operated by Parascandolo
and Sons. Some of the permits and sites for the traps date back to colonial times (Clay et
al. 2008).
2. There are three major fishing related businesses here. Sakonnet Lobster is a lobster
wholesaler located in Sakonnet Point adjacent to the harbor (Clay et al. 2008). The Point
Trap Company and H.N. Wilcox Inc. are primarily engaged in trap fishing (Little
Compton Harbor Commission 2008).
3. The fishery at Sakonnet Point is small but highly diverse. According to the Sakonnet
Harbor Management Plan, there are currently approximately 30 commercial fishing
vessels based in the harbor, which may include both vessels with federal permits and
vessels with state permits (Little Compton Harbor Commission 2008). According to
NMFS, in 2009 there were 17 vessels with federal permits home ported in the Sakonnet
Point/Little Compton area (NMFS 2010e). There are also one or two transient fishing
vessels that use the harbor regularly. About three quarters of these vessels engage in
commercial lobstering, primarily from April through November. The remainder of the
boats target finfish or shellfish using a variety of different gear types including fish traps.
Vessels that fish in the winter months primarily engage in gillnetting, and many of the
harbor’s lobster boats can be adapted for this use (Little Compton Harbor Commission
2008). The most valuable commercial species landed at Sakonnet Point in recent years
have included monkfish, summer flounder, scup, black sea bass, and lobster (Clay et al.
2008).
530.2.4. Block Island
1. Block Island has a small commercial fishing presence; in 2009, there were 10 federally
licensed fishing vessels listed as having their home port in Block Island (NMFS 2010e).
Similar to Sakonnet Point, the most valuable commercial species landed at Block Island
9 Data are not available on what percentage of the vessels in Newport harbor might engage in recreational fishing
activities.
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in recent years have included monkfish, summer flounder, scup, black sea bass, and
lobster (Clay et al. 2008).
2. Block Island is an important port for recreational fishing, with at least seven charter boats
listed for the island. There are several recreational fishing tournaments held out of Block
Island each year (Clay et al. 2008). Consultation with Rhode Island recreational fishing
stakeholders has indicated that many recreational fishing vessels, including charter boats,
docked at other ports in Rhode Island frequently fish the waters around Block Island.
530.2.5. Other Commercial and Recreational Fishing Ports
1. While Rhode Island does have several other ports involved in fisheries, the vast majority
of commercial fishing activity out of other ports takes place within Narragansett Bay
(e.g. quahogging) and is thus outside of the Ocean SAMP waters. However, there are a
few other fishing vessels scattered around Narragansett Bay that may make use of or pass
through the Ocean SAMP area. North Kingstown, Tiverton, and Jamestown all have a
small number of lobster boats that may fish within Rhode Island Sound. Warren has a
couple of hydraulic dredge clam boats that fish for ocean quahogs in the waters south of
the Ocean SAMP area at around 35 to 40 fathoms; if quahog populations rebound in
Rhode Island and Block Island Sounds, they may again fish this area.
2. In the Davisville area of North Kingstown there are two large freezer trawlers owned by
Sea Freeze that target squid, herring, mackerel, and butterfish within the Ocean SAMP
area as well as further offshore. The most valuable species landed in North Kingstown in
recent years have included squid and mackerel. Port-specific landings value data are not
available for North Kingstown as this information is kept confidential by NMFS in order
to protect the privacy of the one major company located in this port (Clay et al. 2008).
3. Numerous other ports throughout the state serve an important role for recreational
fisheries, as recreational vessels docked at any location throughout Rhode Island may
occasionally or frequently fish within the Ocean SAMP area. As noted above, the
majority of the state’s recreational fishing party and charter boats are based out of Point
Judith and, to a lesser extent, Newport. Point Judith and Newport also provide dockage
and support services for numerous private recreational fishing vessels that operate in the
Ocean SAMP area. In addition, many private recreational fishing vessels that operate in
the Ocean SAMP area are based in the ports of Sakonnet Point and Block Island
(discussed above), as well as Charlestown, Westerly, Wickford, Warwick, and East
Greenwich (R. Hittinger, pers. comm. a).
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530.3. Description of Rhode Island’s Fisheries
1. For the purposes of the Ocean SAMP, fisheries have been divided up into commercial
and recreational fisheries. Commercial fisheries is further divided into two categories –
mobile gear and fixed gear fisheries. Mobile gear fisheries are those in which fishing
gear such as an otter trawl is deployed while in motion aboard a vessel, while fixed gear
fisheries employ static gear such as lobster pots, fish pots, and gillnets, which are set in
one location and then retrieved later. The term recreational fisheries is used here to
describe both recreational anglers and recreational fishing aboard private boats and party
and charter boats. See Section 530.7 below for further discussion.
530.3.1. Bottom Types, Seasonal Migrations, and Fishing
1. Commercial and recreational fishing activity can be further characterized by the
fisherman’s target species and the benthic features, or bottom types, which may present
the fishermen with the best possible harvest of those species. Many migrating bottom
species congregate in areas of habitat change, known as transition zones or “edges,”
whenever possible because they can exploit the benefits of both habitats in order to find
food or shelter, or for reproductive purposes. Transition zones include, but are not limited
to, the edges that represent changes from mud to sand, sand to gravel, gravel to boulders,
and boulders to ledge. In the Ocean SAMP area, many targeted species make seasonal
migrations from offshore to inshore, and back offshore; each transition zone provides a
point in that migration where fish can stop and exploit the benefits of both habitat types.
Fishermen know these seasonal migratory patterns as well as the tendency of fish to
congregate in these transition zones, and concentrate their fishing effort accordingly.
2. These migratory patterns are particularly pronounced for species such as lobster that are
targeted by fixed gear fishermen (both lobstering and gill-netting), and so transition
zones such as moraines and moraine edges are especially important to these fishermen.
Transition zones of other bottom types can be equally important to fixed gear fishermen
following fish on their seasonal migrations. Mobile gear fishermen such as bottom
trawlers also follow fish on their seasonal migrations and seek to exploit transition zones,
although the nature of bottom trawling limits the types of bottom that can be trawled, and
so these fishermen only exploit transition zones that are conducive to this gear type. In
the Ocean SAMP area, most bottom trawling takes place on smooth bottom types (e.g.
sand, mud, and gravel), although some trawlers with rockhopper gear occasionally trawl
in areas with boulders. See Chapter 2, Ecology of the Ocean SAMP Region for further
discussion of moraines and other benthic features, as well as a broader discussion of the
geology and benthic ecology of the Ocean SAMP area.
530.3.2. Mapping Fisheries Activity Areas
1. Commercial and recreational fishing takes place throughout most of the Ocean SAMP
area. A two-part approach was taken to map fishing activity for inclusion in the Ocean
SAMP document. First, commercial and recreational fishing activity was characterized
and mapped through qualitative input from fishermen. In a series of interviews and
meetings that took place in 2008-2009, Rhode Island commercial and recreational
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fishermen were asked to indicate, on nautical charts, areas where they fish (see Appendix
B for detailed methodology). Second, commercial fishing activity was characterized and
mapped through analysis of quantitative fisheries-dependent data collected from 1998 -
2008. As a means of monitoring fisheries activity, NMFS requires commercial fishermen
with federally-permitted groundfish, scallop, and monkfish vessels to submit one Vessel
Trip Report (VTR) for each fishing trip. On each report, the fisherman reports the
location of that trip as one set of coordinates (latitude/longitude or Loran). These maps
were created by aggregating the VTRs of all RI-based vessels using these gear types from
1998 – 2008 as a set of point data, and then creating a density plot using a 1-minute by 1-
minute grid overlay to determine the relative density of fishing trips. Darker-shaded areas
represent the areas with a higher density of fishing activity. Although these VTR maps
are based on quantitative data, they must still be viewed with caution. VTR location
information is only an approximation of fishing activity because the fisherman self-
reports only one set of coordinates for the trip, despite the fact that one trip may include
multiple tows that take place in many different locations across a much wider area.
2. Figure 5.17 shows total fishing activity based on qualitative input from fishermen.
Figure 5.18 shows total commercial mobile gear and gillnet fishing based on NMFS VTR
data. Additional maps are provided in the subsequent sections below to illustrate fishing
activity by gear type. See Appendix B for a detailed methodology and additional maps.
Together, these mapping processes resulted in a series of maps that create an accurate
approximation of many types of Ocean SAMP area fishing activity. However it is
important to note that fishing is a very dynamic activity and as such is inherently difficult
to capture through a static mapping exercise. Fishing effort varies widely throughout the
year, and from year to year, depending on the individual fisherman, vessel type, target
species, regulatory environment, and market demand. In addition, fishing effort varies in
location and intensity throughout the year because fishermen follow their target species
on their seasonal migrations. A number of the targeted species move within the Ocean
SAMP area, while others move into and out of the Ocean SAMP area, throughout the
course of a year.
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Figure 5.17. Mobile gear, fixed gear, and recreational fishing areas based on qualitative input.
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Figure 5.18. Commercial mobile gear and gillnet fishing areas based on NMFS Vessel Trip Reports, 1998 - 2008.
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530.4. Contemporary Commercial Mobile Gear Fisheries
530.4.1. Description
1. Commercial fishing activity in the Ocean SAMP area can mostly be divided into two
categories – mobile gear and fixed gear fisheries. Mobile gear fisheries are those in which
the fishing gear is being actively employed from a vessel while capturing the fish, as
opposed to fixed (static) gear, which is set in one location to fish and then retrieved later
(for more on fixed gear fisheries, see Section 530.5). Commercial mobile gear fishing
methods employed in fisheries in the Ocean SAMP area include: bottom and mid-water
trawling (also called dragging), dredging, purse seining, and rod and reel fishing. While
the majority of mobile gear fishing taking place within the Ocean SAMP area is by
Rhode Island-based vessels, fishing vessels from other states, including Massachusetts,
Connecticut, and New York, will frequently transit through or fish in the federal waters
of the Ocean SAMP area.
2. One of the most common and traditional methods for fishing within the Ocean SAMP
area is otter trawling (commonly referred to as dragging), in use in Rhode Island since the
1930s. Trawlers fishing within the Ocean SAMP area are primarily either day boats or
short-trip boats (at sea from one to three days). Species traditionally targeted by the
trawlers in the Ocean SAMP area include squid, butterfish, fluke, scup, hake, cod,
monkfish, yellowtail flounder, and winter flounder. Rhode Island fishermen, more so
than fishermen from elsewhere in New England, typically fish for “mixed species”
throughout much of the year, including squid, butterfish, and scup, or whiting (silver
hake), all of which are fished with an otter trawl. Squid are at present the most important
fishery to Rhode Island fishermen, both in terms of landings value and landed weight (see
Section 530.6 for further discussion). Most of the fishing for squid takes place outside the
Ocean SAMP area by large trawlers. However, from May through September or October,
squid can often be found within the northern Ocean SAMP area in the waters south of
Point Judith and Charlestown. Many of the smaller inshore draggers as well as some
larger vessels from Rhode Island ports will focus on this fishery during these months, and
vessels will sometimes come from Massachusetts to target these squid as well. During
those months, this is an important fishery for the dayboat fleet. Whiting, or silver hake, is
another important fishery for Rhode Island fishermen, who will fish for it all year long,
frequently within the southern portions of the Ocean SAMP area. Many of the Rhode
Island fishermen will target groundfish species when available. Most of the groundfish
targeted in the Ocean SAMP area are flounder and are harvested from the smoother
bottom areas south of Block Island. Codfish catches within the Ocean SAMP area have
been improving in recent years and are a late winter/early spring target. Skates are both a
directed fishery and bycatch. In the Ocean SAMP area, most bottom trawling takes place
on smooth bottom types (e.g. sand, mud, and gravel), although some trawlers with
rockhopper gear occasionally trawl in areas with boulders.
3. Rhode Island mid-water trawlers will fish in the Ocean SAMP area for herring and
mackerel in the fall and winter months; purse seine vessels are also used to target herring.
Other vessels from ports including Massachusetts, Maine, New Jersey, and North
Carolina come to Rhode Island Sound just for this season. When the herring are close to
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shore, a number of vessels will participate in this fishery. This is an important fishery for
small boats in Rhode Island during the months these fish are in the area.
4. A number of vessels with general access scallop permits, which limit them to 400 pounds
of scallops per day, may fish in the Ocean SAMP area. Scalloping is traditionally done
using a dredge towed behind the vessel. These boats make up a small percentage of total
sea scallop landings for Rhode Island, but this is an important fishery for vessels without
limited access permits for scallop. This fishery is generally restricted to smaller boats that
take day trips to the southern part of the Ocean SAMP area.
5. There is a commercial rod and reel harvest in the Ocean SAMP area for striped bass,
tuna, scup, and fluke. According to the RIDEM state license reports, vessels with
commercial rod and reel permits operating in statistical area 539 made 8,304 trips in
2007, 9,699 trips in 2008, and 8,882 in 2009. In all three years commercial rod and reel
trips represented the largest number of fishing trips made by any single gear type; see
Table 5.35 (RIDEM 2010b).
530.4.2. Mobile Gear Fisheries Activity Areas
1. Mobile gear fishing takes place throughout most of the Ocean SAMP area.
Characterizing the locations of fishing activity requires both qualitative input from
fishermen as well as analysis of NMFS fisheries dependent datasets. Together, these data
create an accurate approximation of mobile gear fishing activity. However it is important
to note that fishing is a very dynamic activity and as such is inherently difficult to capture
through a static mapping exercise. Fishing effort varies widely throughout the year, and
from year to year, depending on the individual fisherman, vessel type, target species,
regulatory environment, and market demand. In addition, fishing effort varies in location
and intensity throughout the year because fishermen follow their target species on their
seasonal migrations. A number of the targeted species move within the Ocean SAMP
area, while others move into and out of the Ocean SAMP area throughout the course of a
year.
2. Figure 5.19 shows mobile gear fishing areas based on qualitative input from fishermen.
See Appendix B for the methodology used to develop these maps. All of the areas shown
as mobile gear fishing areas are used at some point in the course of the fishing season.
Because of the dynamic nature of fishing described above, all mobile gear fishing areas
are not in use all of the time. This does not, however, diminish the importance of the use
of these areas.
3. Figures 5.20, 5.21 and 5.22 show bottom trawling, scallop dredging, and mid-water
trawling areas based on NMFS Vessel Trip Report data. As noted above, bottom trawling
and scallop dredging are the two main types of mobile gear fishing in the Ocean SAMP
area. As a means of monitoring fisheries activity, NMFS requires commercial fishermen
with federally-permitted groundfish, scallop, and monkfish vessels to submit one Vessel
Trip Report (VTR) for each fishing trip. On each report, the fisherman reports the
location of that trip as one set of coordinates (latitude/longitude or Loran). These maps
were created by aggregating the VTRs of all RI-based vessels using these gear types from
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1998 – 2008 as a set of point data, and then creating a density plot using a 1-minute by 1-
minute grid overlay to determine the relative density of fishing trips. Darker-shaded areas
represent the areas with a higher density of fishing activity. Although these VTR maps
are based on quantitative data, they must still be viewed with caution. VTR location
information is only an approximation of fishing activity because the fisherman self-
reports only one set of coordinates for the trip, despite the fact that one trip may include
multiple tows that take place in many different locations across a much wider area. See
Appendix B for a more detailed discussion of data sources and methodology.
4. A comparison of Figure 5.19 (which represents both methods of mobile gear fishing)
with Figures 5.20-5.22 reveals that these maps create a relatively consistent depiction of
mobile gear fishing in the Ocean SAMP area. Bottom trawling is concentrated in the
waters between Block Island and the mainland, as well as the waters south and southeast
of Block Island. Scallop dredging is concentrated in the furthest offshore parts of the
Ocean SAMP area, including waters south and southwest of Block Island and the Cox
Ledge area.
5. Mobile gear fishermen follow their target species on their seasonal migrations and work
the areas with bottom type suitable to their gear types. For example, while much dragging
takes place in areas with soft bottom, some scallop dredging takes place in rockier areas.
One fishing area of particular importance is Cox Ledge, which is used by mobile gear as
well as fixed gear and recreational fishermen. Distinct polygons shown within the shaded
mobile gear areas represent areas that are only used by mobile gear fishermen during
certain parts of the year; these areas are used during other times of the year by fixed gear
fishermen through informal cooperative agreements between fishermen. See Section
530.5 for further discussion of fixed gear fisheries, and Section 530.7 for further
discussion of recreational fisheries.
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Figure 5.19. Mobile gear fishing areas based on qualitative input.
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Figure 5.20. Bottom trawling areas based on NMFS Vessel Trip Reports, 1998 - 2008.
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Figure 5.21. Scallop dredging areas based on NMFS Vessel Trip Reports, 1998 - 2008.
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Figure 5.22. Mid-water trawling areas based on NMFS Vessel Trip Reports, 1998 - 2008.
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530.5. Contemporary Commercial Fixed Gear Fisheries
530.5.1. Description
1. Rhode Island has a number of significant fixed gear commercial fisheries. These include
gillnetting as well as trap fisheries, which includes the use of lobster pots, fish pots, and
floating fish traps (which are used within state waters). These fisheries are primarily near
shore fisheries, conducted on day trips using smaller vessels, usually with a crew of only
one or two fishermen. Because these fisheries tend to occur near shore, the vast majority
take place within the Ocean SAMP area. Also, because of the nearshore nature of these
fisheries, the majority of fishermen and vessels participating in this fishery are based out
of Rhode Island.
2. Fishing for lobster using traps is common throughout the Ocean SAMP area; most
lobsters landed within Rhode Island are caught in this area. Lobster fishing is generally
seasonal, and takes place primarily from the spring through late December. Lobster
fishing within the Ocean SAMP area is commonly done by small boats with a crew of
one or two, while offshore lobstermen will travel further out beyond the Ocean SAMP
area to fish the canyons. Lobster boats are permitted to set up to 800 traps, and typically
a boat will set a few dozen strings of 15-25 traps each. Before 1950, lobsters were
primarily taken as incidental catches in trawls for demersal finfish. Of lobsters landed in
Rhode Island, 98.5% are taken with traps, and the remaining 1.5% by otter trawl
(DeAlteris et al. 2000).
3. Rhode Island has a significant floating fish trap fishery concentrated in state waters.
Figure 5.23 shows currently active or permitted fish trap locations. Most floating fish
traps are located off Sakonnet and Newport, and off of Narragansett and Pt. Judith. It
should be noted that there are additional possible fish trap locations that are identified in
RI DEM regulations but not presently active.10 Floating fish trap catch includes scup,
squid, striped bass, and other migratory fish. Floating fish trap fishermen would be
seriously affected if these targeted fish were diverted to other areas.
4. Gillnets make up an important segment of the state’s fixed gear fisheries. Gillnet
fishermen target a number of species including groundfish, scup, bluefish, fluke, and
skate. Gillnets are also the primary gear used in the monkfish fishery; a large majority of
the Rhode Island monkfish fishery takes place within the Ocean SAMP waters. There are
a number of gillnet fishermen out of Sakonnet Point who fish primarily within the Ocean
SAMP area.
10 See RI Marine Fisheries Statutes and Regulations, Part XIV – Fish Traps, online at
http://www.dem.ri.gov/pubs/regs/regs/fishwild/rimf14.pdf , for further information on fish trap locations.
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Figure 5.23. Currently active or permitted floating fish trap areas.
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530.5.2. Fixed Gear Fishing Activity Areas
1. Fixed gear fishing, which here includes fishing with lobster pots, fish pots, and gillnets,
also takes place throughout most of the Ocean SAMP area. As noted above in section
530.4.2, characterizing the locations of fishing activity requires both qualitative input
from fishermen as well as analysis of NMFS fisheries dependent datasets. Fixed gear
fisheries are similar to mobile gear fisheries in that fishing effort varies widely
throughout the year, and from year to year, depending on the individual fisherman, vessel
type, target species, and regulatory environment. In addition, fishing effort varies in
location and intensity throughout the year because fishermen follow their target species
on their seasonal migrations.
2. Figure 5.24 shows fixed gear fishing areas based on qualitative input from fishermen.
See Appendix B for the methodology used to develop these maps. All of the areas shown
as fixed gear fishing areas are used at some point in the course of the fishing season,
though not all fixed gear fishing areas are not in use all of the time. One fishing area of
particular importance is Cox Ledge, which is used by fixed gear as well as mobile gear
and recreational fishermen. Distinct polygons shown within the shaded fixed gear areas
represent areas that are only used by fixed gear fishermen during certain parts of the
year; these areas are used during other times of the year by mobile gear fishermen
through informal cooperative agreements between fishermen. See Section 530.4 for
further discussion of mobile gear fisheries, and Section 530.7 for further discussion of
recreational fisheries.
3. Figure 5.25 shows gillnetting areas based on NMFS Vessel Trip Report data. As noted
above, gillnetting and lobstering are the two main types of fixed gear fishing in the Ocean
SAMP area. NMFS requires commercial fishermen with federal-permitted vessels to
submit one Vessel Trip Report for each fishing trip; each VTR includes self-reported
location information about the trip. It is important to note that no Vessel Trip Report
data, or equivalent data, are available for lobstering. NMFS does not collect VTRs from
lobstermen because the lobster fishery is managed by the ASMFC (see Section 510.2.1).
Whereas RIDEM collects logbook data from lobstermen, these data include location
information reported by statistical area, not by latitude/longitude or Loran, which do not
allow for a fine-resolution analysis of lobstering activity. See Section 530.3.2 above and
Appendix B for further discussion of data sources and methodology.
4. In Figure 5.25, darker-shaded areas represent the areas with a higher density of
gillnetting activity. This map reveals that some gillnetting is concentrated in a couple of
areas just outside the mouth of Narragansett Bay, whereas other gillnetting activity is
concentrated much further offshore in the waters southeast and east of Block Island and
in the Cox Ledge area. It is difficult to accurately compare Figures 5.24 and 5.25 given
the absence of VTR lobstering data.
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Figure 5.24. Fixed gear fishing areas based on qualitative input.
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Figure 5.25. Gillnetting areas based on NMFS Vessel Trip Reports, 1998 - 2008
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530.6. Rhode Island Commercial Fisheries Effort and Landings
530.6.1. Rhode Island Commercial Fisheries Landings
1. Commercial fisheries landings data presented below are provided by the National Marine
Fisheries Service, Fisheries Statistics Division. Landings data for the state of Rhode
Island is dealer-reported; seafood dealers within the state report twice per week to the
Standard Atlantic Fisheries Information System (SAFIS) on the pounds and ex-vessel
dollar value of landings sold at each dealer.11 These data encompass all landings taking
place at Rhode Island ports. Vessels based in Rhode Island may at times land their catch
outside of the state, in New Bedford, for example. Likewise, some of the landings in
Rhode Island may be from vessels based outside of the state; during the winter months,
boats from New Jersey and other Mid-Atlantic states will fish in Rhode Island waters,
and land their catch here. Landings data do not include where the catch was actually
harvested. Thus, it is not possible to differentiate among catch from within the Ocean
SAMP area or outside of the Ocean SAMP area.
2. Much of the effort data provided here, given as the numbers of trips taken by vessels and
the number of trips on which vessels caught certain species, are provided only for Rhode
Island state fishing licenses. This means these data include only vessels targeting certain
species managed at the state level, such as lobster and herring, or vessels fishing only
within state waters (within three miles of shore). Thus, much of the activity taking place
within the Ocean SAMP area, including fishing done through federally-permitted vessels
and fishing done by out-of-state vessels, is not encompassed in this effort data provided
below. In lieu of effort data for federal waters, included below are federal data on the
pounds and dollar value of Rhode Island landings, broken down by gear type, which
provide some insight into fishing effort. These landings data reflect federally permitted
vessels which land their catch in Rhode Island.
3. The top fishery in Rhode Island averaged for the years 1999-2008 by weight was Atlantic
herring, followed by loligo (longfin) squid and Atlantic mackerel (see Table 5.34).12 The
squid fishery in Rhode Island has been and continues to be an important and profitable
fishery in the state. Herring and mackerel are taken in midwater trawls, and are part of an
important fishery occurring within the Ocean SAMP area. The next species by weight is
skates, which are taken in large numbers but are often considered a trash fish or used as
bait (little skate and winter skate are also listed individually; the skates category includes
both species, and if the three are combined, the average landings are more than those for
mackerel). Of all Rhode Island commercial fisheries, finfish caught in Narragansett Bay
account for only 5%, meaning the remaining 95% of finfish landings were caught in the
Ocean SAMP area or beyond. Likewise, Narragansett Bay accounts for about 10-25% of
11 The Standard Atlantic Fisheries Information System (SAFIS) is an electronic reporting system developed by the
National Marine Fisheries Service (NMFS) and the Atlantic Coastal Cooperative Statistics Program.
12 “Other shellfish” is the term used by NMFS to report some shellfish landings. NMFS landings data are sometimes
classified broadly in this way (finfish or shellfish) in order to protect the confidentiality of dealers purchasing the
species. See NMFS Fisheries Statistics Division. 2009. “Data Caveats.” Online at
http://www.st.nmfs.noaa.gov/st1/commercial/landings/caveat.html.
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all lobster landings, leaving the remaining 75-90% to the Ocean SAMP area and further
offshore (DeAlteris et al. 2000).
Table 5.34. Top landed species in Rhode Island by weight for 1999-2008.13 (ACCSP 2010)
Note: Important species in the Ocean SAMP area are italicized. Average dollar value calculated based on
each year’s nominal landings value, which do not account for inflation.
Species
Average Pounds
1999-200814
Average Dollar
Value 1999-2008
Number of
Years
Landed
Herring, Atlantic
19,426,667
$1,637,564
10
Squid, Longfin inshore
18,426,084
$14,018,015
10
Mackerel, Atlantic
7,623,878
$1,921,248
10
Skates
6,455,051
$627,053
10
Hake, Silver
6,290,385
$2,543,255
10
Goosefish (Monkfish)
5,148,746
$4,921,970
10
Lobster, American
4,340,526
$19,113,035
10
Scup
3,131,617
$2,381,122
10
Squid, Northern shortfin
3,089,620
$882,507
6
Skate, Little
2,374,344
$196,849
6
Flounder, Summer
2,158,836
$4,660,022
10
Butterfish
1,588,842
$680,673
10
Flounder, Winter
1,173,497
$1,599,963
10
Crab, Atlantic rock
952,517
$489,484
8
Flounder, Yellowtail
941,055
$1,067,699
10
Crab, Jonah
892,223
$471,098
10
Quahog, Northern
890,965
$5,675,621
10
Hake, Red
797,796
$191,042
10
Scallop, Sea
719,914
$4,847,792
10
Crab, Red
608,303
$452,849
6
Bluefish
553,631
$185,447
10
Crabs, Brachyura
484,718
$242,149
7
Cod, Atlantic
454,363
$511,321
10
Dogfish, Spiny
409,938
$71,208
10
Haddock
336,594
$369,411
10
Menhadens
326,289
$38,916
10
Bass, Black sea
315,991
$758,978
10
Skate, Winter
217,973
$42,254
6
Bass, Striped
202,593
$540,829
10
Surfclam, Atlantic
181,261
$6,272
1
Flounder, Witch
168,881
$211,958
10
Plaice, American
119,517
$118,531
10
Clam, Soft
102,742
$711,869
10
13 Includes all species landed in Rhode Island for 1999-2008, both within and outside of the Ocean SAMP area,
where average pounds landed over the ten year period is more than 100,000. Some species included here are
primarily caught outside of the SAMP area.
14 Shellfish weights are expressed in meat weights
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5. Figures 5.26 and 5.27 below show average landings of species both by pounds and by
value for all of Rhode Island for the years 1999-2008. Landings by pounds are dominated
by Atlantic herring, followed by longfin (loligo) squid and mackerel. The most valuable
landings for this period, on the other hand, were of lobster, followed by longfin squid.
See Section 540.1 for more on the value of commercial fisheries landings within Rhode
Island.
Top Fifteen Species by Pounds Landed 1999-2008
LITTLE SKATE
2.9%
BUTTERFISH
1.9%
FLOUNDER, WINTER
1.4%
CRAB, ATLANTIC
ROCK
1.1%
FLOUNDER, SUMMER
2.6%
FLOUNDER,
YELLOWTAIL
1.1%
SCUP
3.8%
SQUID, NORTHERN
SHORTFIN
3.7%
LOBSTER, AMERICAN
5.2%
GOOSEFISH
6.2%
HAKE, SILVER
7.6%
SKATES
7.8%
MACKEREL, ATLANTIC
9.2%
SQUID, LONGFIN
INSHORE
22.2%
HERRING, ATLANTIC
23.4%
Figure 5.26. Top landed species in Rhode Island by weight, 1999-2008 (includes fish caught both within
and outside of the Ocean SAMP area). (ACCSP 2010)15
15 Shellfish weights are expressed in meat weights
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Top Fifteen Species by Average Landings Value 1999-2008
SQUID, LONGFIN
INSHORE
21.0%
QUAHOG, NORTHERN
8.5%
GOOSEFISH
7.4%
HERRING, ATLANTIC
2.5%
FLOUNDER,
YELLOWTAIL
1.6%
SCUP
3.6%
FLOUNDER, WINTER
2.4%
MACKEREL, ATLANTIC
2.9%
HAKE, SILVER
3.8%
FLOUNDER, SUMMER
7.0%
SCALLOP, SEA
7.3%
BASS, BLACK SEA
1.1%
CLAM, SOFT
1.1%
SQUID, NORTHERN
SHORTFIN
1.3%
LOBSTER, AMERICAN
28.6%
Figure 5.27. Top landed species in Rhode Island by dollar value averaged for 1999-2008 (includes fish
caught both within and outside of the Ocean SAMP area). (ACCSP 2010)
Note: Average dollar value calculated based on each year’s nominal landings value, which do not
account for inflation.
5. Figure 5.28 below shows a longer-term time series of total commercial fisheries landings
by weight from 1970 - 2008. Landings increased to a high in the early and mid-1990s,
and have been declining since then.
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Total Commercial Landings in Pounds, 1970-2008
0
20,000,000
40,000,000
60,000,000
80,000,000
100,000,000
120,000,000
140,000,000
160,000,000
1970
1972
1974
1976
1978
1980
1982
1984
1986
1988
1990
1992
1994
1996
1998
2000
2002
2004
2006
2008
Year
Pounds
Landings
Figure 5.28. Rhode Island landings by weight, 1970-2008 (includes fish caught both within and outside
of the Ocean SAMP area). (NMFS, Fisheries Statistics Division 2009a)
530.6.2. Rhode Island Commercial Fishing Effort
1. Commercial fisheries effort is defined as the amount of fishing activity that takes place
within a specified period of time. Effort is typically quantified by the number of fishing
trips, and/or the number of “days at sea” (as defined by the management regime, not a
calendar day). Data provided below includes the numbers of trips on which various
species were caught, indicating how often those species are harvested, although not
necessarily how often they are targeted. Effort is also not indicative of the volume of
catch. Data are also provided for the weight and dollar value for landings of various gear
types, indicating which types of fisheries produce the greatest harvest and have the
greatest economic value within the state. Some of the data provided below are only for
state-licensed vessels, while others are for federally permitted fisheries.
2. Table 5.35 below lists species caught in 2007-2009 in NMFS statistical area 539 by
vessels with state permits, and the number of trips within each month on which those
species were caught. See Figure 5.29 for a map showing statistical area 539. Only species
caught on an average of 50 or more trips in a given year are included. These data include
only species landed with a state permit, and therefore include only species caught within
state waters, including Narragansett Bay, and do not include species caught within
federal waters of the SAMP area, or by vessels possessing federal permits. This means
these data do not reflect the majority of activity taking place in the SAMP area. These
numbers reflect effort, but not necessarily abundance, as certain fisheries may be closed
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during certain times of the year (e.g. monkfish, tautog), and effort may be shifted
elsewhere during that month.
Table 5.35. Average number of trips on which species were landed (state data only – includes trips both
within and outside of the Ocean SAMP area), 2007-2009 (RIDEM 2010b).
Species
Jan
Feb
Mar
Apr
May
Jun
Jul
Aug
Sep
Oct
Nov
Dec
Total
Summer
Flounder
3
3
4
107
1,663
1,753 2,142 1,252
18
2
35
7
6,989
Lobster,
American
215
115
122
225
479
1,050 1,624 1,279 650
428
394
317
6,898
Scup
2
2
66
364
388
1,126
957
812
383
82
8
4,190
Black Sea Bass
2
3
1
25
375
345
558
895
478
278
82
1
3,044
Striped Bass
1
9
60
1,299
93
71
451
108
4
2
2,096
Bluefish
2
100
272
308
319
230
124
41
7
1,402
Tautog
1
114
316
2
130
147
9
294
116
3
1,131
Skate
7
4
9
49
245
185
132
71
38
24
26
8
798
Winter Flounder
11
2
6
89
246
86
56
24
21
18
28
10
598
Squid, Loligo
11
19
174
84
54
35
12
5
21
7
422
Conger Eel
2
4
2
3
11
16
70
153
80
59
16
1
418
Butterfish
6
8
100
69
43
14
14
8
19
3
284
Gray
Triggerfish
11
71
85
64
26
1
258
Monkfish
3
2
4
7
48
49
30
12
6
11
26
5
200
Menhaden
15
45
61
35
20
10
5
4
3
199
Sea Robin
11
73
49
36
17
4
1
3
3
198
American Eel
2
4
28
17
14
25
33
27
13
11
174
Spiny Dogfish
50
58
32
12
8
3
1
163
Crab, Jonah
7
3
7
9
16
23
22
18
19
12
9
6
151
Weakfish
7
31
22
19
13
9
6
3
110
Crab, Rock
1
2
2
5
10
15
22
16
12
6
4
4
98
Smooth Dogfish
2
30
30
16
8
7
1
95
Windowpane
Flounder
2
1
19
43
11
8
1
7
1
92
Cunner
5
3
6
25
21
17
5
84
Hickory Shad
3
12
26
25
12
5
2
83
Bonito
7
16
27
20
13
82
Cod
5
3
7
11
11
4
6
4
4
4
13
5
77
Winter Skate
1
5
12
15
6
13
6
3
7
68
False Albacore
1
14
39
13
67
Crab, Green
3
5
3
1
6
23
13
2
55
Red Hake
3
2
1
12
17
4
2
3
4
5
2
54
Horseshoe Crab
5
14
21
7
1
1
1
1
51
Silver Hake
7
1
10
13
8
2
1
4
4
50
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Figure 5.29. NMFS Statistical Areas.
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3. Prior to 2007, RI DEM only collected data on lobster trips; these data are available from
2003 to 2006. In 2003, 8,964 lobster trips took place in NMFS Statistical Area 539; 8,812
trips in 2004; 10,226 trips in 2005; and 10,797 trips in 2006 (RIDEM 2010b). Though
these data represent too few years to indicate a trend, they suggest a short-term increase
in the number of lobster trips in Area 539.
4. Table 5.36 and Figure 5.30 below show what types of fishing gear have been used most
commonly by Rhode Island fishermen over the last decade, and how much they land for
each gear type, both by pounds and the dollar value of landings. The gear used by Rhode
Island fishermen to catch the most fish by weight is the otter trawl, and the value of
species landed by otter trawl is the highest among all gear. In addition to the groundfish
species such as cod and flounders landed with an otter trawl, the small-mesh net otter
trawl is used in Rhode Island’s squid fishery, which is why this gear represents more than
50% of landings by weight. The next gear type weight is the paired midwater trawl,
followed by pots and traps (other), which may include some lobster landings as well as
squid landings. Ranked second by value of landings among gear types is inshore lobster
pots and traps, which averaged over $9 million in landings over this time period.
5. Of the gear types listed below, most are used either predominantly or partially in the
Ocean SAMP area. Most of the lobster traps are fished in the Ocean SAMP area, and fish
pots and gillnets occur almost exclusively in the Ocean SAMP area.16
Table 5.36. Rhode Island landings by gear type, 1999-2008 (includes fish caught both within and outside
of the Ocean SAMP area). (NMFS, Fisheries Statistics Division 2009a)
Note: Average dollar value calculated based on each year’s nominal landings value, which do not
account for inflation.
Gear
Average Landings in
Pounds 1999-2008
Average Dollar Value of
Landings 1999-2008
Otter Trawl, Bottom, Fish
59,131,329
$29,159,418.80
Trawl Midwater, Paired
10,380,727
$686,795.60
Pots And Traps, Other
9,968,096
$6,567,691.60
Not Coded/Other
7,898,880
$9,646,535.00
Otter Trawl, Midwater
7,649,674
$480,073.40
Gill Nets
4,245,477
$3,386,439.60
Pots And Traps, Lobster Inshore
2,446,071
$9,148,139.80
Dredge, Clam
1,874,640
$1,095,295.80
Pots And Traps, Lobster Offshore
1,780,073
$5,687,875.70
Dredge, Other
1,775,492
$4,312,557.70
Floating Traps (Shallow)
983,610
$776,261.70
Rakes
812,491
$4,556,840.90
Lines Hand, Other
654,659
$1,144,331.30
Pound Nets
364,243
$297,889.00
Purse Seines
297,909
$12,837.30
Long Lines
275,902
$636,117.20
Pots And Traps, Fish
186,843
$237,619.80
16 NMFS and RI DEM use different categories for differentiating fishing activity by gear type (see Table 5.36
below). For this reason it is not possible to accurately compare federal and state data by gear type.
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Dredge, Sea Scallop
173,667
$947,181.00
Diving Outfits, Other
171,106
$856,444.80
Lines, Troll, Other
62,752
$21,311.30
Hoes
61,181
$351,099.00
Tongs
38,513
$214,584.30
By Hand, Other
35,083
$90,976.00
Otter Trawl, Bottom, Other
28,628
$52,474.60
Average Landings by Gear Type 1999-2008
Otter Trawl
58.9%
Paired Midwater
Trawl
9.1%
Rakes
0.7%
Hand Lines
0.6%
Dredge
3.9%
Diving
0.2%
Not Coded/Other
6.9%
Pots and Traps
14.4%
Gill Nets
3.7%
Floating Traps
(Shallow)
0.9%
Long Lines
0.2%
Purse Seines
0.3%
Pound Nets
0.3%
Figure 5.30. Rhode Island landings in pounds by gear type for 1999-2008 (includes fish caught both
within and outside of the Ocean SAMP area). (NMFS, Fisheries Statistics Division 2009a)17
6. Table 5.37 below displays average commercial fishing effort for 2007-2009 in NMFS
Statistical Area 539 for vessels with state permits. This table shows the number of trips
per month by gear type, this time broken out into the number of fishing trips taken with
each gear type for each month. These data show that commercial rod and reel trips were
most prevalent during 2007-2009, and lobster trips were the second most common type
of commercial fishing activity. As stated above, these data are only for state fisheries,
and include fishing effort within Narragansett Bay. These numbers indicate the frequency
with which these gear types are used, which is very different than the above table
illustrating the pounds of fish taken by each gear type, and the value of the landings
taken with each gear type.
17 Some gear types are combined in this figure, and gear types with fewer than 500,000 pounds of landings are
excluded.
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Table 5.37. Average number of trips per month by gear type, 2007-2009 (includes trips taken both within
and outside of the Ocean SAMP area) (state fishing licenses only).18 (RIDEM 2010b)
Gear Type
Jan
Feb
Mar
Apr
May
Jun
Jul
Aug
Sep
Oct
Nov
Dec
Total
Rod & Reel
3
3
7
49
1057
2546
2085
1542
974
544
144
8
8962
Pots & Traps
(Lobster)
207
112
119
209
423
959
1496
1201
642
430
384
314
6496
Pots & Traps
(Fish)
2
2
2
7
115
191
544
555
464
263
50
4
2198
Gillnet
2
1
6
97
455
247
208
121
38
55
29
4
1262
Otter Trawl
18
9
9
28
238
216
237
154
54
26
40
20
1050
Floating Fish
Trap
19
95
77
69
54
35
19
2
370
Other
6
7
8
27
37
50
39
26
20
18
20
6
262
18 2007 is the most recent data provided by RI DEM and the only year for which complete finfish and crustacean
data are available. RI DEM did not collect data on species other than lobsters prior to 2007. Please note that monthly
effort is affected by closures and other regulatory measures. .
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530.7. Contemporary Recreational and For-Hire Fishing
530.7.1. Description
1. Recreational fishing, which here includes both recreational fishing that takes place
aboard for-hire party and charter boats as well as recreational anglers from shore or
aboard private boats, has a long history in Rhode Island. Marine recreational fishing is a
major recreational activity for Rhode Islanders as well as a major tourist attraction that
brings in visitors from out-of-state. Recreational fishing also has a significant economic
impact on the state, which is discussed below in Section 540.2. Recreational fishing in
the Ocean SAMP area is done both from shore and by boat, including both private
vessels and party and charter boats. Whereas there is a great deal of recreational fishing
that takes place within Narragansett Bay, this section is focused primarily on fishing that
takes place outside of the Bay in offshore waters.
2. Recreational fishermen, or anglers, who fish aboard private vessels or from shore, are
regular users of the Ocean SAMP area. According to NMFS, the most common
recreationally targeted species in marine waters in RI include Atlantic bonito, Atlantic
cod, black sea bass, bluefish, scup, striped bass, summer flounder, tautog, winter
flounder, and yellowfin tuna (NMFS 2008b). A different recreational fishing study,
commissioned by the RIDEM, found striped bass and bluefish to be the two most popular
species targeted by recreational anglers in Rhode Island. This survey includes anglers
fishing both within and outside of Narragansett Bay. The most popular shore sites for
fishing according to this survey were all bordering along the Ocean SAMP area, and
include shore sites in Narragansett, Newport, and Jamestown (RIDEM 2006).
3. Some recreational fishermen who fish in the Ocean SAMP area only fish there
occasionally, while others are regular users of the area. The Rhode Island Saltwater
Anglers Association (RISAA), which is the largest recreational fishing organization in
the state, estimates that of its 1,800 members, approximately 30% fish outside of
Narragansett Bay in the Ocean SAMP area on a regular basis – roughly once a week -
whereas 70% of their members fish in the Ocean SAMP area at least once a year. RISAA
further estimates that there are recreational fishing vessels from every RI coastal town
that use the Ocean SAMP area. Almost half of all boaters who use the Ocean SAMP area
launch their boats directly from Point Judith boat ramps (Hittinger, pers. comm. a).
4. Recreational fishermen may also participate in organized fishing tournaments. RISAA
currently sponsors 15 special fishing tournaments each year. According to RISAA, of
these events, the Fluke, Team Fluke, Junior Catch and Release All-Species, Cod, Black
Sea Bass, Bluefish/Striped Bass Combo, and Fall Bluefish/Striper Catch and Release
tournaments all involve a significant amount of fishing in the Ocean SAMP area. In
addition, RISAA sponsors a “Yearlong Tournament” which targets 15 different species.
According to RISAA, of these species, the cod, haddock, striper, false albacore, bonito,
pollock, tuna, mahi mahi, and fluke categories are usually won by a fish caught in the
Ocean SAMP area (RISAA 2010; Hittinger, pers. comm. b).
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5. Most of the RI-based party and charter boats that run fishing trips regularly operate in the
Ocean SAMP area. Charter boats are for-hire vessels operated by a licensed captain and
crew, usually carrying up to six passengers who have hired out the boat for the entire trip.
A party or head boat, on the other hand, is typically a larger vessel where passengers pay
individually for a space fishing on the vessel. The Rhode Island Party and Charter Boat
Association has 70 members, and there are other charter boats in Rhode Island that are
not a part of the association (Bellavance pers. comm.). However, many of the boats
belonging to the association and most of the boats that are not members fish only on a
limited basis. One member of the association estimated that about 30 party and charter
boats are actively fishing, each making at least 30 trips each year (Donilon, pers. comm.).
All of these vessels fish within the Ocean SAMP area for most or all of the year,
although they move to different fishing grounds based on the time of year and the species
they are targeting. The vast majority of the charter boats are based in Galilee, with one
or two in Watch Hill, and one or two located further up in Narragansett Bay. The charter
boats located in the Upper Bay often fish in the Bay instead of going out to the Ocean
SAMP area, but they do fish in the Ocean SAMP area, as do the boats in the Lower Bay
(Rainone, pers. comm.).
6. Table 5.38 below lists the number of charter and party boat licenses issued each year
since 1999, when the licensing program took effect. The license is for two years; thus in
2009, there are 240 active charter and party boat licenses within the state of Rhode
Island, reflecting those issued in 2008 - 2009.
Table 5.38. Party and charter boat licenses issued by year. (RIDEM 2010b)
Year
1999
2000
2001
2002
2003
2004
2005
2006
2007
2008
2009
Licenses
90
21
31
24
29
27
36
63
167
94
146
7. There are five party boats fishing out of Rhode Island, all of them based in Galilee. The
larger party boat operation runs about 700 trips each year, and carries approximately
18,000 passengers a year (Blount, pers. comm.).
530.7.2. Recreational Fishing Catch and Effort Data
1. Recreational fishing catch, effort, economic impact, and activity areas are generally more
difficult to characterize than those of commercial fishing because, generally speaking,
less information on recreational fishing is collected and published by federal and state
regulatory agencies. This is in part because there is no federal recreational fishing
licensing program currently in place in the northeastern U.S., though it should be noted
that the National Saltwater Angler Registry and the Rhode Island Recreational Saltwater
Fishing License Program, both of which took effect in 2010, are both designed to
improve recreational fishing data collection.19
2. This section and Section 540.2, below, include the most recent and best available existing
data and information that has been published to date by federal and state agencies and
19 See https://www.countmyfish.noaa.gov/index.html for further information on the National Saltwater Angler
Registry and http://www.dem.ri.gov/programs/bnatres/fishwild/reclic.htm for further information on Rhode Island’s
Recreational Saltwater Fishing License Program.
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other parties. Recreational data sources used here and in Section 540.2 include the NMFS
Marine Recreational Fisheries Statistics Survey program (MRFSS) (updated through
2008). The MRFSS program provides data extrapolated from surveys administered to a
sampling of recreational fishermen. The MRFSS program consists of two independent
surveys - an intercept survey of marine anglers at fishing access sites, and a random digit
dial telephone survey conducted in coastal counties. Survey results are then extrapolated
to estimate fishing effort across the nation. Because of these methods and the associated
margin of error, these data should be viewed as estimates, rather than verifiable facts.
Moreover, the MRFSS data must be interpreted with additional caution, as
methodological issues have recently been identified with the program’s survey methods,
such that NMFS is developing a new program to gather data on recreational fishing.20
However, because the MRFSS data are among the few available datasets to characterize
recreational fishing, they may be considered the best available data and are included here
for illustrative purposes. In this section and Section 540.2 below, MRFSS data are
supplemented with other data and information provided in recent surveys and reports,
though it should be noted that these documents and all other sources should also be
viewed with caution insofar as they include survey-based estimates of recreational
fishing activity.
3. Figure 5.31 and Table 5.39 below show average estimated recreational catch, by species,
for 1999 – 2008, as illustrated by MRFSS data. These data include only fish caught in the
ocean waters, including both federal and state waters, and not fish caught within
Narragansett Bay. Striped bass and summer flounder (fluke) are the two most commonly
caught species, followed by bluefish and scup. Although bluefish and striped bass are
often cited as the two most commonly targeted recreational species within the state,
much of the fishing for these species takes place within the waters of Narragansett Bay.
These data are only projected estimates of catch, and have a large standard error
associated with the projected numbers.
20 In 2006 the National Research Council studied the MRFSS program and identified several problems with the
program, including issues a lack of resources and problems with the sampling and survey methods. See National
Research Council. 2006. “Report in Brief: Review of Recreational Fisheries Survey Methods.” Online at
http://dels.nas.edu/dels/rpt_briefs/rec_fish_brief_final.pdf. Because of these issues, the MRFSS program will be
replaced with the Marine Recreational Information Program (MRIP).
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Estimated Average Recreational Catch (lbs), 1999-2008
(Excludes Narragansett Bay)
Summer flounder
23.9%
Bluefish
19.7%
Striped bass
29.1%
Atlantic cod
2.6%
Other
1.3%
Other tunas/
mackerels
1%
Black sea bass
3.3%
Tautog
5.2%
Scup
13.0%
Atlantic mackerel
0.6%
Dolphins/Mahi-mahi
0.4%
Striped bass
Summer flounder
Bluefish
Scup
Tautog
Black sea bass
Atlantic cod
Other tunas/mackerels
Atlantic mackerel
Dolphins/Mahi-mahi
Other
Figure 5.31. Estimated average recreational catch by species, 1999-2008, based on MRFSS data. (Pers.
comm., NMFS Fisheries Statistics Division, MRFSS, 2010)
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Table 5.39. Estimated average recreational catch, 1999-2008, based on MRFSS data. (Pers. comm.,
NMFS Fisheries Statistics Division, MRFSS, 2010)
4. According to the MRFSS program, it is estimated that during 1999-2008, an average of
nearly 385,000 people participated in recreational ocean fishing in RI each year, making
over 785,000 fishing trips yearly. These figures include both RI residents and out-of-state
fishermen; for this time period, an average of approximately 143,000 (37%) Rhode
Islanders and 242,000 out-of-state residents (63%) fished in RI ocean waters. These data
include only recreational fishing in ocean waters, including both federal and state waters,
and not fishing within Narragansett Bay. As these figures are estimates, they vary
considerably from year to year. Figure 5.32 and 5.33 below show the number of trips and
participants from 1999-2008, as well as the annual breakdown of participants by
residency. Together, these figures show that while the number of trips varies year to year,
participation in recreational fishing has generally been growing over the past decade.
Figure 5.33 also illustrates how out-of-state fishermen consistently comprise the majority
of recreational fishermen fishing in RI ocean waters. For more information on the
economic impact of these activities, see Section 540.2 below.
Species Name
Average catch (lbs)
Striped bass
835,941
Summer flounder
687,416
Bluefish
566,135
Scup
374,226
Tautog
149,944
Black sea bass
94,146
Atlantic cod
74,431
Other tunas/mackerels
22,096
Atlantic mackerel
18,499
Dolphins (Mahi mahi)
12,493
Winter flounder
11,650
Little tunny/Atlantic bonito
8,573
Other sharks
4,234
Other fishes
2,612
Dogfish sharks
1,953
Weakfish
1,721
Skates/rays
1,468
Cunner
1,197
Herrings
1,085
Other cods/hakes
853
Red hake
678
Pollock
652
Triggerfishes/filefishes
574
Sea robins
345
Other jacks
266
Spanish Mackerel
130
Sculpins
29
Eels
20
King mackerel
7
Other flounders
2
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5. Figure 5.34 shows the breakdown of recreational fishing trips by mode. These data
include only recreational fishing in ocean waters, including both federal and state waters,
and not fishing within Narragansett Bay. Shore-based fishing makes up nearly 50% of
recreational ocean fishing trips in Rhode Island. Fishing by private boat, whether owned
or rented, makes up over 45% of saltwater fishing trips within the state, and many of
these trips will take place in the Ocean SAMP area. Party and charter boat fishing (for-
hire fishing), while having the smallest number of trips of the three fishing modes
surveyed, occurs almost entirely in the Ocean SAMP area.
Estimated Recreational Fishing Trips and Participants,
1999-2008
(Excludes Narragansett Bay)
0
100,000
200,000
300,000
400,000
500,000
600,000
700,000
800,000
900,000
1,000,000
1999
2000
2001
2002
2003
2004
2005
2006
2007
2008
Year
Number Trips
Participants (total)
Figure 5.32. Estimated recreational fishing trips and participants, 1999-2008. (Pers. comm., NMFS
Fisheries Statistics Division, MRFSS, 2010)
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Estimated Recreational Fishing Participants by Residency,
1999-2008
(Excludes Narragansett Bay)
0
50,000
100,000
150,000
200,000
250,000
300,000
350,000
400,000
450,000
500,000
1999
2000
2001
2002
2003
2004
2005
2006
2007
2008
Year
Number of participants
Out-of-state residents
RI residents
Figure 5.33. Estimated recreational fishing participants by residency, 1999-2008. (Pers. comm., NMFS
Fisheries Statistics Division, MRFSS, 2010)
Estimated Recreational Fishing Trips by Mode, 1999-2008
(Excludes Narragansett Bay)
0
100,000
200,000
300,000
400,000
500,000
600,000
700,000
800,000
900,000
1,000,000
1999 2000 2001 2002 2003 2004 2005 2006 2007 2008
Year
Number of trips
Private/Rental
Party/Charter
Shore
Figure 5.34. Estimated recreational fishing trips by mode, 1999-2008, based on MRFSS data. (Pers.
comm., NMFS Fisheries Statistics Division, MRFSS, 2010)
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530.7.3. Recreational and For-Hire Fishing Activity Areas
1. Recreational fishing takes place throughout much of the Ocean SAMP area. For the
Ocean SAMP, recreational fishing has been characterized primarily through qualitative
input from recreational fishermen. Figure 5.35 shows areas based on qualitative input
from fishermen. Recreational fishing areas shown on this map represent both private
recreational fishing and recreational fishing aboard for-hire party and charter boats. See
Appendix B for the methodology used to develop these maps. It should be noted that
fishermen involved in this mapping effort clearly indicated that all state waters
surrounding Block Island were heavily used for recreational fishing. Other fishing areas
of particular importance to recreational fishermen are the waters southwest of Block
Island, including Southwest Ledge, and Cox Ledge. Like commercial fishing,
recreational fishing effort varies widely throughout the year, and from year to year,
depending on the individual fishermen, vessel type, target species, regulatory
environment, and seasonal migrations of target species.
2. During the late spring, Rhode Island-based party and charter boats are almost
exclusively targeting cod, which have started to make a recovery to numbers suitable
for recreational fishing. Most fishing for cod is done on Cox Ledge and south of Block
Island. Earlier in the spring season, the majority of party and charter boats target the
migratory stocks of the mid-Atlantic such as striped bass, summer flounder, and black
sea bass. During the summer, most recreational fishing is focused on striped bass and
bluefish, with some boats targeting fluke closer to shore. Later in the summer, some of
the recreational fishing boats will move further offshore to target sharks, which are
generally caught anywhere from 20 to 50 miles offshore. Sharks targeted include blue,
mako, thresher, and hammerhead sharks, and most shark fishing is catch and release.
Some tuna fishing also takes place within an area east of Block Island and northwest of
Cox Ledge known as the Mud Hole (often called Deep Hole by commercial fishermen).
Starting in September, much of the fishing switches to sea bass and scup around Block
Island, or to striped bass closer to shore at that time of year.
3. Some out-of-state party and charter boats from Connecticut, Massachusetts, and New
York also regularly fish within the Ocean SAMP area. Some of these boats fish in
Rhode Island state waters surrounding Block Island, target striped bass on Southwest
Ledge off the southwest corner of the island and summer flounder in various areas
around the island. Some of these boats also fish for scup, black sea bass, and tuna in
federal waters south of Block Island (Bellavance, pers. comm.).
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Figure 5.35. Recreational and charter boat fishing areas based on qualitative input.
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Section 540. Economic Impact of Commercial and Recreational Fisheries
1. Commercial and recreational fisheries are both significant contributors to Rhode Island’s
economy. However, it is not possible to directly and accurately compare the values of
commercial fisheries and recreational fishing. For commercial fisheries, the value of the
fishery is primarily determined by the value of the fish landed within the state, regardless
of where the fish were caught. Some economic analyses of commercial fisheries may
also consider related activities, such as seafood processing and distribution, employment,
and the multipliers associated with commercial fishing. By contrast, recreational fishing
cannot be assessed by fish landed as many fish are not landed at all (but are caught
through catch-and-release fishing), and none are sold on the market. Instead, the
economic value of recreational fishing is in the act of fishing itself, and as such is
measured by assessing the industry itself – i.e. income and employment associated with
charter boat businesses, boat manufacturers, and tackle shops.
540.1. Commercial Fisheries Landings Value and Economic Impact
1. Commercial fishing is an important contributor to the state’s economy. The economic
contribution of commercial fishing is determined by the landings values of the fish
landed within the state, the export of fisheries products, the impact of processing,
distribution, and retail, the resulting employment, and other factors. The section below
includes discussion of the ex-vessel revenue associated with commercial fisheries
landings, and also summarizes available data on the broader economic impact of
commercial fisheries to RI.
2. Because of the nature of fisheries activity and fisheries data, it is not possible to directly
attribute a dollar amount to the contribution of fisheries in the Ocean SAMP area.
Commercially harvested species that are landed in RI ports may be harvested anywhere;
conversely, species harvested in the Ocean SAMP area may be landed in an out-of-state
port and accounted for in that state’s landings data. This section summarizes information
about the value of all state landings as well as the economic impact of commercial
fishing to the state. Where possible, distinctions are made to emphasize the particular
value of Ocean SAMP area fishing to the state of Rhode Island.
3. A 2008 study conducted by NMFS found that ex-vessel revenue from commercial
fisheries landings increased 41% (adjusted for inflation) from 1997 through 2006 in New
England. This increase was largely due to an increase in revenue from shellfish – the
revenue from finfish landings decreased in this period. The total landings revenue in
Rhode Island in 2006 was roughly $98.6 million. This included $28 million in revenue
for finfish landings, and more than $70 million in revenue for shellfish landings (which
includes sea scallops, lobster, and squid) (NMFS 2008a).21
4. Table 5.39 below shows that the most valuable landings on average in Rhode Island for
1999-2008 were lobster ($19,113,035), followed by loligo squid ($14,018,015), northern
quahogs ($5,675,621), monkfish ($4,921,970), and sea scallops ($4,847,792). The most
21 At the time of this writing, NMFS “Fisheries Economics of the United States 2006” is the most recent commercial
fisheries economic study available.
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valuable species per pound on average was oysters at $14.35/pound, followed by sea
scallops, averaging $6.73/pound, northern quahogs at $6.37/pound, and lobster at
$4.40/pound. These figures include all ports in Rhode Island, and include species
targeted both within and outside of the Ocean SAMP area, including Narragansett Bay.
Of the species listed, all but oysters and quahogs are currently fished for within the
Ocean SAMP area.
Table 5.40. Top landed species in Rhode Island by value averaged for 1999-2008 (includes fish caught
both within and outside of the Ocean SAMP area).22 (ACCSP 2010)
Note: Ocean SAMP area commercially important species highlighted. Data on landings values by port
are based on the NOAA Fisheries commercial dealer weigh out data, which includes the pounds landed
and sold to the dealer, and the total price paid for each species. Average dollar value was calculated
using the annual nominal landings value, which does not account for inflation.
Species
Average Pounds
Landed 1999-
200823
Average Dollar Value
1999-2008
Average Price per
Pound
Lobster, American
4,340,526
$19,113,035
$4.40
Squid, Longfin inshore
18,426,084
$14,018,015
$0.76
Quahog, Northern
890,965
$5,675,621
$6.37
Goosefish (Monkfish)
5,148,746
$4,921,970
$0.96
Scallop, Sea
719,914
$4,847,792
$6.73
Flounder, Summer
2,158,836
$4,660,022
$2.16
Hake, Silver
6,290,385
$2,543,255
$0.40
Scup
3,131,617
$2,381,122
$0.76
Mackerel, Atlantic
7,623,878
$1,921,248
$0.25
Herring, Atlantic
19,426,667
$1,637,564
$0.08
Flounder, Winter
1,173,497
$1,599,963
$1.36
Flounder, Yellowtail
941,055
$1,067,699
$1.13
Squid, Northern shortfin
3,089,620
$882,507
$0.29
Bass, Black sea
315,991
$758,978
$2.40
Oyster, Eastern
50,676
$742,558
$14.65
Clam, Soft
102,742
$711,869
$6.93
Butterfish
1,588,842
$680,673
$0.43
Skates
6,455,051
$627,053
$0.10
Bass, Striped
202,593
$540,829
$2.67
Cod, Atlantic
454,363
$511,321
$1.13
Crab, Atlantic rock
952,517
$489,484
$0.51
Crab, Jonah
892,223
$471,098
$0.53
Crab, Red
608,303
$452,849
$0.74
Haddock
336,594
$369,411
$1.10
Crabs, Brachyura
484,718
$242,149
$0.50
Swordfish
85,632
$236,487
$2.76
Flounder, Witch
168,881
$211,958
$1.26
Skate, Little
2,374,344
$196,849
$0.08
Hake, Red
797,796
$191,042
$0.24
Bluefish
553,631
$185,447
$0.33
22 Species included in the table are those for which the average landings value is over $100,000 for 1999-2008
23 Shellfish weights are expressed in meat weights
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Plaice, American
119,517
$118,531
$0.99
Whelk, Channeled
93,273
$118,367
$1.27
5. Figure 5.36 below shows trends in landings and landings value in Rhode Island for the
years 1999-2008. The dollar values here are nominal values only, and not adjusted for
inflation, and therefore are weighted toward the more recent years. Landings have
decreased over that time period, while the landings values have seen less fluctuation.
Rhode Island Federal Landings 1999-2008 (Weight and Value)
0
20,000,000
40,000,000
60,000,000
80,000,000
100,000,000
120,000,000
140,000,000
1999
2000
2001
2002
2003
2004
2005
2006
2007
2008
Year
Weight in Pounds/ Value in Dollars
Pounds
Value ($)
Figure 5.36. Rhode Island commercial landings by value, 1999- 2008 (includes fish caught both within
and outside of the Ocean SAMP area). (NMFS, Fisheries Statistics Division 2009a)
Note: dollar values are annual nominal landings values only and are not adjusted for inflation.
540.1.1. Point Judith
1. Clay et al. (2008) report that in 2006, there were 168 vessels with federal permits in Point
Judith, and the total federal landings value in Point Judith was $46,947,791 (see Table
5.41). The most valuable federally managed group of species was squid, mackerel, and
butterfish (combined into one group for management purposes), with a 2006 landings
value of $13,188,211, followed by lobster, with landings of over $8.6 million (see Table
5.42).24
24 Clay et al. 2008 represents the most recently published and best available data on port-specific landings and value.
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Table 5.41. Federal vessel permits and landings value between 1997 and 2006 for Point
Judith/Narragansett (includes fish caught both within and outside of the Ocean SAMP area). (Clay et al.
2008)
Year
# Vessels
Value of landings in Point Judith ($)
1997
181
$47,529,746
1998
175
$42,614,251
1999
181
$51,144,479
2000
184
$41,399,853
2001
186
$33,550,542
2002
179
$31,341,472
2003
173
$31,171,867
2004
174
$36,016,307
2005
171
$38,259,922
2006
168
$46,947,791
Table 5.42. Dollar value of landings of federally managed groups of species for Point Judith (includes
fish caught both within and outside of the Ocean SAMP area). (Clay et al. 2008)
Average from 1997 – 2006
2006 only
Squid, Mackerel, Butterfish
$11,298,781
$13,188,211
Lobster
$11,022,301
$8,675,086
Summer Flounder, Scup, Black
Sea Bass
$4,718,136
$6,495,568
Smallmesh Groundfish25
$2,816,677
$1,799,479
Monkfish
$2,687,563
$2,110,227
Largemesh Groundfish26
$2,451,647
$3,383,452
Other27
$2,056,576
$2,697,425
Scallop
$1,457,702
$7,420,396
Skate
$618,033
$604,990
Herring
$470,065
$376,506
Tilefish
$230,142
$32,985
Bluefish
$112,378
$118,466
Dogfish
$48,031
$45,000
Red Crab
$9,593
$0
2. Figure 5.37 shows Point Judith commercial landings by weight and value from 1999-
2008. The dollar values here are nominal values only, and not adjusted for inflation, and
therefore are weighted toward the more recent years. The landings by weight indicate
that whereas landings declined from 1999-2001, they have since remained fairly
consistent.
25 Smallmesh Multi-Species: red hake, ocean pout, mixed hake, black whiting, silver hake (whiting)
26 Largemesh groundfish: cod, winter flounder, witch flounder, yellowtail flounder, American plaice, sand-dab flounder,
haddock, white hake, redfish, and pollock
27 “Other” species includes any species not accounted for in a federally managed group, including species managed at the
state level
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Point Judith Landings by Weight and Value, 1999-2008
0
10
20
30
40
50
60
70
80
Year
1999
2000
2001
2002
2003
2004
2005
2006
2007
Year
Landings
Pounds (millions)
Dollar Value (Millions)
Figure 5.37. Point Judith landings by dollar value and weight, 1999-2008. (NMFS 2009a)
Dollar values are annual nominal landings values only and are not adjusted for inflation.
540.1.2. Newport
1. Clay et al. (2008) report that in 2006, there were 48 vessels with federal licenses listing
Newport as their home port, and the total value of landings was $20,837,561 (see Table
5.43).28 The most valuable species landed in Newport in 2006 was scallops, with a
landed value of $13,267,494, followed by lobster, worth just under $3 million (Clay et al.
2008) (see Table 5.43).
Table 5.43. Federal vessel permits and landings value between 1997 and 2006 for Newport (includes fish
caught both within and outside of the Ocean SAMP area). (Clay et al. 2008)
Year
# Vessels
Value of landings in Newport ($)
1997
52
7,598,103
1998
52
8,196,648
1999
52
8,740,253
2000
59
8,296,017
2001
52
7,485,584
2002
55
7,567,366
2003
52
9,082,560
2004
52
8,402,556
2005
54
14,281,505
2006
48
20,837,561
28 Clay et al. (2008) represents the most recent and best available data on port-specific landings and value.
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Table 5.44. Dollar value for landings of federally managed species for Newport (includes fish caught
both within and outside of the Ocean SAMP area). (Clay et al. 2008)
Average from 1997-2006 ($)
2006 only ($)
Lobster
2,758,908
2,971,680
Scallop
2,528,448
13,267,494
Squid, Mackerel, Butterfish
1,425,947
1,315,229
Largemesh Groundfish29
1,039,962
445,273
Monkfish
878,265
1,068,547
Summer Flounder, Scup, Black
Sea Bass
739,880
815,918
Other30
334,103
401,779
Smallmesh Groundfish31
179,296
43,165
Skate
58,481
224,184
Herring
42,538
267,164
Dogfish
26,441
6,037
Red Crab
15,560
0
Bluefish
11,759
9,878
Tilefish
9,230
1,213
2. Figure 5.38 shows Newport commercial landings and value from 1999-2008. The dollar
values are nominal values only and are not adjusted for inflation, and therefore are
weighted toward the more recent years. Whereas the value of Newport’s landings seems
to have fluctuated, the weight of landings stayed relatively consistent from 2004-2007.
Newport Landings by Weight and Dollar Value, 1999-2008
(No data available for 1999-2003)
0
5
10
15
20
25
1999
2000
2001
2002
2003
2004
2005
2006
2007
2008
Year
Landings
Pounds (millions)
Dollar Value (millions)
Figure 5.38. Newport landings by dollar value and weight, 1999-2008. (NMFS 2009a)
29 Largemesh groundfish: cod, winter flounder, witch flounder, yellowtail flounder, am. plaice, sand-dab flounder,
haddock, white hake, redfish, and pollock
30 “Other” species includes any species not accounted for in a federally managed group, including species managed at the
state level
31 Smallmesh Multi-Species: red hake, ocean pout, mixed hake, black whiting, silver hake (whiting)
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3. Figure 5.39 and Figure 5.40 track the ranking of Point Judith and Newport amongst all
major U.S. fishing ports by both landings value and pounds landed. Point Judith has
steadily been declining in ranking of pounds landed since 1998 and in landings value,
although landings value has fluctuated more than pounds. The rank of Point Judith did
climb in 2008 from 21st to 18th in value of landings, and from 24th to 21st in pounds.
Newport did not appear in the rankings for 1999-2003. Newport climbed significantly in
the rankings for both pounds landed and landings value for 2006, but declined again in
2007. Data for Newport for 2008 were not available (NMFS 2009a).
Ranking by Pounds of Commercial Fishery Landings
at Major U.S. Ports
(No data available for Newport 1999-2003)
0
10
20
30
40
50
60
70
1999 2000 2001 2002 2003 2004 2005 2006 2007 2008
Year
Ranking among major U.S. ports
Point Judith
Newport
Figure 5.39. Ranking by pounds of commercial fishery landings at major U.S. ports, 1999-2008. (NMFS
2009a)
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Ranking by Dollar Value of Commercial Fishery Landings at
Major U.S. Ports
0
10
20
30
40
50
60
70
80
1999 2000 2001 2002 2003 2004 2005 2006 2007 2008
Year
Ranking among major U.S. ports
Point Judith
Newport
Figure 5.40. Ranking by dollar value of commercial fishery landings at major U.S. ports, 1999-2008.
(NMFS 2009a)
4. While commercial fisheries landings have great value in themselves, the commercial
fishing industry has a broader effect on Rhode Island’s economy through the jobs,
income, and sales associated with the commercial fishing industry. However,
accurately assessing the economic impact of the state’s commercial fishing industry is
difficult for a variety of reasons, including the fact that many fishermen are self-
employed and fishing vessels do not always land their catch in the same state in which
they are home ported. For this reason, estimates of the economic impact of commercial
fishing vary by study. One 2008 study analyzed 2006 landings and employment data
and determined that the RI commercial fishing industry represents approximately 1700
jobs and nearly $98 million in wages, and accounted for $11-18 million in vessel
operation costs and another $9-15 million in vessel maintenance costs. In total, this
study found that the state’s commercial fishing industry is responsible for at least $100
million in economic activity each year (RI Economic Monitoring Collaborative 2008).
5. A 2008 NMFS fisheries economic study found that the estimated total sales impacts
from the Rhode Island commercial fishing industry were approximately $705,938,000,
and the estimated income impacts from this industry state-wide totaled $378,396,000
(see Table 5.45). The majority of economic impacts in both areas came from the
resulting impacts on the retail sectors of seafood sales. Commercial harvesting itself
also provided significant economic impacts to the economy, with more than $75
million in income impacts to the state, and over $3 million in employment impacts
(NMFS 2008a).32 Once again, because it is not feasible to determine the amount or
value of landings originating within the Ocean SAMP area, it is impossible to
32 This NMFS study, Fisheries Economics of the United States 2006, is at the time of this writing the most updated
and best available data on the economic impact of commercial fishing throughout the region.
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determine what percentage of these impacts can be attributed to fishing activity and
resources found within the Ocean SAMP area.
Table 5.45. Economic impacts of commercial fishing industry in Rhode Island, 2006. (NMFS 2008a)
Sales Impacts
Income Impacts
Employment Impacts
Commercial Harvesters
$171,075,000
$75,223,000
$3,308,000
Seafood Processors and
Dealers
$50,924,000
$18,474,000
$465,000
Seafood Wholesalers and
Distributors
$97,988,000
$50,549,000
$947,000
Retail Sectors
$385,951,000
$234,149,000
$10,246,000
Total Impacts
$705,938,000
$378,396,000
$14,966,000
6. A 2009 NMFS economic study of marine-related industries (Thunberg 2009) provides
additional insight into the broader economic impacts of commercial fishing. According to
this study, the number of establishments in Rhode Island involved in seafood commerce
was 112 in 1999, and declined to 92 in 2005 (see Table 5.46).33 Seafood commerce
includes commercial fishing, seafood dealers, seafood processors, and retail seafood
markets. The number of employees in these establishments was 2,291 in 1999, and fell to
1,925 by 2005 (see Table 5.46). In 2005, 68.0% of employment in the seafood commerce
sector was made up of commercial fishing employees, 16.2% was made up of seafood
dealers, 14.0% was in the processing sector, and 7.3% was in seafood retail. There were a
total of 1,211 sole proprietors engaged in fishing in Rhode Island in 2005, and Rhode
Island fishermen in sole proprietorships earned more than the average for the Northeast
region. At the same time, wage-based income was higher for fishermen than income
earned through a sole proprietorship in Rhode Island, but lower in many other Northeast
states. The consumer price index adjusted annual fishing wages in Rhode Island in 2005
averaged $31,546, while the adjusted average receipts for sole proprietorships in 2005
were $27,954 (Thunberg 2009).
Table 5.46. Total number of Rhode Island seafood commerce establishments and employees, 1999-2005.
(Thunberg 2009)
.
7. This 2009 NMFS study also analyzed fishing-related employment in Rhode Island and
found Bristol, Newport, and Washington Counties all had a fishing quotient higher than
33 This NMFS study, Trends in Northeast Region Marine Industries (Thunberg 2009) is based on data through 2005
and provides the most recent and best available data on commercial fishing-related businesses in RI.
Year
Number of
Establishments
Number of Employees
1999
112
2,291
2000
110
2,240
2001
112
2,235
2002
104
2,057
2003
104
2,225
2004
105
2,057
2005
92
1,925
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one, meaning fishing employment in these counties is higher than average, and these
three counties would be disproportionately affected by a reduction in fishing
employment. In 2005, the number of fishing employees and sole proprietorships in
Bristol County was 76; in Newport County, 198; and in Washington County, 176
(Thunberg 2009).
8. NMFS further analyzed employment at seafood dealer establishments and found that in
2005, total employment in Rhode Island in the seafood dealer sector was 206 at 32
seafood dealer establishments. Rhode Island had as many as 66 seafood dealer
establishments in 1993, but this number declined steadily through the 1990s and early
2000s. Overall, Rhode Island had more residents employed by seafood dealers as a
percentage of all employment state-wide than the average for most Northeast states, and
Newport and Washington Counties had the highest dependence on seafood dealer
employment, with 61 employees in eight establishments in Newport County, and 70
employees in 12 establishments in Washington County in 2005 (Thunberg 2009) (see
Table 5.47).
9. NMFS also investigated seafood processing establishments and found that Rhode Island
had seven such businesses in 2005, employing 270 people. Like for seafood dealers, the
percentage employment in seafood processing is generally higher in Rhode Island than
the average employment in the sector for the Northeast. In 2005, Bristol County had two
seafood processors with 192 employees, Newport County had two seafood processors
with 63 employees, and Washington County had one processor with two employees.
Rhode Island had 31 retail seafood markets in 2005 with 140 employees, which, again,
was higher than the average employment for the Northeast (Thunberg 2009) (see Table
5.47).
Table 5.47. Fisheries sector employment impacts, 2005. (Thunberg 2009)
Sector
Bristol
County
Newport
County
Washington
County
RI
Total
Number of
Establishments
N/A
8
12
32
Seafood Dealers
Employees
N/A
61
70
206
Number of
Establishments
2
2
1
7
Seafood Processors
Employees
192
63
2
270
Number of
Establishments
3
3
5
31
Retail Seafood
Market
Employees
5
23
34
140
540.2. Economic Impact of Recreational Fishing
1. While recreational fishing is different than commercial fishing in that fish caught are not
landed and sold on the market, it nonetheless has a significant economic impact in the
state of Rhode Island. Unlike commercial fishing, the value of recreational fishing lies in
the act of fishing itself, and the expenditures associated with that act. As noted above in
Section 530.7.2, recreational fishing catch, effort, and associated economic impact are
generally more difficult to characterize because of the lack of data collected by state and
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federal regulatory agencies. Estimates of the economic impact of recreational fishing are
typically based on surveys administered to a sampling of recreational fishermen and
extrapolated to a larger population, combined with analysis of the businesses (e.g. tackle
shops and boat manufacturers) associated with recreational fishing. Results of these
studies tend to vary widely depending on the sample size and location, methods, and data
sources used. For these reasons, all recreational fishing data should be regarded with
caution and should be viewed as estimates, rather than verifiable facts.
2. Several studies have attempted to extrapolate from survey results to create estimates of
the economic impact of recreational fishing in Rhode Island. One such study was
conducted by NMFS in connection with the Marine Recreational Fisheries Statistics
Survey (MRFSS) program, discussed above in Section 530.7.2. Economic data on fishing
expenditures were gathered from an economic survey added on to the traditional MRFSS
survey; this was performed in 2006 (Gentner and Steinback 2008).34 Other economic
impact studies of RI recreational fishing include one commissioned by the Rhode Island
Saltwater Anglers Association (RISAA) which incorporated 2006 angler intercept survey
results as well as MRFSS and other pre-existing data sets (Ninigret Partners 2007), and
one conducted by the U.S. Fish and Wildlife Service in 2006. Together, these studies
represent the best available and most up-to-date recreational fishing economic impact
data for Rhode Island; results of each study are summarized below. As is the case for
commercial fishing data, it is infeasible to directly apportion a percentage of recreational
fishing activity to within the Ocean SAMP area based on the available data. In addition it
should be noted that the discrepancy between surveys and the lack of clear survey
methods make recreational fisheries economic data difficult to compare with commercial
fisheries economic data.
3. The most recent available recreational fishing economic data from NMFS are
summarized in Fisheries Economics of the United States, 2006 (NMFS 2008a) and
detailed in Gentner and Steinback (2008). In this study, economic intercept surveys were
added onto the traditional MRFSS survey methodology discussed above in Section
530.7.2. This survey includes direct impacts, which occur when anglers spend money at
fishing-related businesses, indirect impacts, based on expenditures by the fishing-related
businesses on supplies and operating costs for their business, and inducted impacts,
which occur when employees in the direct and indirect sectors make purchases as a part
of normal household consumption. The resulting estimates of the multiplier effects from
these activities represent the impacts from saltwater sportfishing expenditures to the
economy (Gentner and Steinback 2008). The data include expenditures by both residents
and non-residents; expenditures by non-residents are higher in Rhode Island than those
for residents, typically because they have to travel further and are more likely to stay
overnight in the state, producing an overall net increase in economic impacts from
saltwater recreational fishing to the state (Gentner and Steinback 2008).
4. This study found that in 2006, recreational anglers spent an estimated $182,606,000 on
recreational fishing. This figure includes both trip expenditures and durable equipment
expenditures. This study estimated that fishermen spent an estimated $60,412,000 on
34 A prior study was conducted in 1998 and published in 2004 (Steinback, Gentner, and Castle 2004). NMFS has
conducted an updated study based on 2008 data, but at the time of this writing, study results are not yet available.
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fishing trips; Rhode Island residents fishing in-state spent $18,727,000, and non-residents
fishing in Rhode Island spent $41,685,000. This study also found that total durable
equipment expenditures for recreational fishing in Rhode Island, including fishing tackle,
other equipment, boats, and the vehicles and second home expenses related to
recreational fishing, at $122,194,000. At over $55 million, fishing tackle represents the
greatest expenditure for recreational fishermen. In addition, because of the costs
associated with owning and operating a boat, boat-based fishing is a significant economic
driver within the state, with $11 million in expenses by residents and an additional $12
million by non-residents. See Tables 5.48 and 5.49 for more information.
Table 5.48. Angler trip expenses, 2006. (NMFS 2008a)
Fishing Mode
Expenditures- non-
residents
Expenditures –
residents
Private Boat
$11,858,000
$11,130,000
Shore
$25,522,000
$6,634,000
For-Hire
$4,305,000
$963,000
Total
$41,685,000
$18,727,000
Table 5.49. Durable equipment expenditures, 2006. (NMFS 2008a)
Durable Equipment
Expenditure
Fishing Tackle
$55,326,000
Other Equipment
$17,367,000
Boat Expenses
$22,042,000
Vehicle Expenses
$25,660,000
Second Home Expenses
$1,799,000
Total Durable Equipment Expenditures
$122,194,000
5. This study also estimated that in 2006, the total impact from RI marine recreational
fishing was $166,869,000 (see Table 5.50). This includes both resident and non-resident
activity. The 2006 estimated value added for Rhode Island based on expenditures was
roughly $82 million, and the 2006 income impact was estimated at over $52 million. This
survey further estimated that 1,476 jobs in Rhode Island are the result of expenditures on
marine recreational fishing, of which 1,001 are the result of direct expenditures (Gentner
and Steinback 2008).
Table 5.50. Economic impacts from recreational fishing in Rhode Island, 2006. (Gentner and Steinback
2008)
Impact Type
Resident
Status
Expenditures
Direct
Impact
Indirect
Impact
Induced
Impact
Total
Impact
Resident
$75,823
$50,586
$14,441
$13,688
$78,684
Non-
Resident
$106,783
$57,765
$14,913
$15,506
$88,184
Output
($1,000)
Total
$182,606
$108,351
$29,324
$29,194
$166,869
Resident
$75,823
$21,312
$8,261
$8,394
$37,967
Non-
Resident
$106,783
$26,535
$7,916
$9,628
$44,079
Value Added
($1,000)
Total
$182,606
$47,847
$16,177
$18,022
$82,046
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Resident
$75,823
$15,247
$4,964
$4,503
$24,714
Non-
Resident
$106,783
$17,588
$4,834
$5,285
$27,707
Income
($1,000)
Total
$182,606
$32,836
$9,798
$9,787
$52,422
Resident
$75,823
414
102
123
639
Non-
Resident
$106,783
587
110
140
836
Employment
(jobs)
Total
$182,606
1,001
212
263
1,476
6. A prior NMFS study using 1998 survey data (Steinback et al. 2004) also assessed the
economic impact of recreational fishing in RI. This study indicated that recreational
fishing supported 1,068 jobs and the total economic impact of recreational fishing
expenditures exceeded $93 million (2000 dollars). Note that this figure is not inflation-
adjusted and therefore cannot be directly compared with the 2006 data presented above.
While small methodological changes make it difficult to compare between this and the
current study on a state-by-state basis, Gentner and Steinback (2008) indicate that for the
nation as a whole, recreational fishing expenditures have increased 79% in comparison to
inflation-adjusted estimates for 2000 (Gentner and Steinback 2008).
7. Another survey based on 2006 survey data, the U.S. Fish and Wildlife Service (FWS)
National Survey of Fishing, Hunting, and Wildlife Associated Recreation, estimated a
total of 158,000 anglers fishing in Rhode Island, of which 82,000 were from out of
state35. These figures, which are much more conservative estimates than those provided
by the MRFSS program (see Section 530.7.2 above), include both saltwater and
freshwater fishing – saltwater fishing only had an estimated 122,000 anglers. This survey
places the total recreational fishing-related expenditures in the state of Rhode Island at
$153,694,000 for both fishing trip and equipment expenses. This total includes both
saltwater and freshwater fishing for an average of $968 per angler. When only saltwater
fishing is considered, the total expenditures are placed at $115,913,000, a considerably
lower estimate than for the MRFSS program (U.S. Fish & Wildlife Service 2006). There
are a few reasons why the NMFS estimates are so much higher than the USFWS survey.
The NMFS survey estimates much higher rates of participation in marine recreational
fishing, in part because of differences in sampling procedures. The NMFS survey targets
marine anglers specifically, as opposed to both salt and freshwater fishing. Additionally,
the NMFS survey contains many more expenditure categories than does the USFWS
survey (Gentner and Steinback 2008).
8. A 2007 recreational fishing economic impact study commissioned by RISAA
incorporated results from an intercept study as well as pre-existing datasets from
numerous other sources including NMFS (1998 data summarized in Steinback et al.
2004) and a 2001 survey conducted by the FWS. This study found that the annual direct
expenditures of RI recreational saltwater anglers are $70 million, and that RI recreational
fishing has a total economic impact of $160 million (Ninigret Partners 2007). These
figures are more conservative than those included in the NMFS and FWS studies
described above; this may be due to the fact that this study included older survey data
than was included in the above-mentioned studies.
35 This U.S. Fish and Wildlife Service survey is conducted every five years.
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Section 550. Impacts of Existing Activities and Trends on Fisheries Resources and
Habitats
1. By definition, fishing impacts fisheries resources, and in some instances, habitats. Other
existing activities that will affect fisheries and fish habitat include, but are not restricted
to: coastal development; introduced species; marine transportation; and marine fisheries
diseases (Johnson et al. 2008). These impacts are discussed below.36
2. Potential future uses of the Ocean SAMP area, which may include offshore renewable
energy development or other activities, may also have impacts on fisheries resources. See
Chapter 8, Renewable Energy and Other Offshore Development, and Chapter 9, Other
Future Uses for further discussion of these issues.
550.1. Fisheries and Overfishing
1. A significant impact on fisheries resources in the Ocean SAMP area comes from fishing
activity. Fishing of any kind will have an effect on the ecosystem. Fishing can have both
primary and secondary impacts on fish populations and species assemblages, including
population declines from overfishing (defined in the Magnuson Stevens Fishery
Conservation and Management Act as fishing at a rate or level or mortality that
jeopardizes the capacity of a fishery to produce the maximum sustainable yield on a
continuing basis) and from shifts in community dynamics.
2. At present, seven of the species of importance to commercial and recreational fisheries
are either listed as overfished or overfishing is occurring on the stock (Atlantic cod,
American lobster, bluefin tuna, tautog, winter flounder, winter skate, and yellowtail
flounder – see Table 5.2 for a list of all species of importance and their status). Many of
the other species found with in the Ocean SAMP area have been in the past or are in
danger of becoming overfished. Overfishing can lead to a reduction in recruitment, or of
fish growing large enough and old enough to spawn, as well as to a decline in the average
size of targeted species (e.g. Collie et al. 2008; Fogarty and Murawski 1998).37
3. Fishing can change the species composition in the food web. The intense harvest of
certain stocks will change the ecological balance of an area by causing the decline of that
stock; that stock’s decline may in turn have an impact on species which relied on the
depleted stock for food, or have an impact on other species which become the new food
source for hungry predators. For example, on Georges Bank, as groundfish populations
have declined, dogfish and skate populations, which target similar prey, exploded
(Fogarty and Murawski 1998). Likewise, a decline in cod populations in the North
Atlantic has led to increased abundance of certain invertebrates such as lobster and crab
that are commonly eaten by cod. Overfishing may also have indirect ecosystem effects,
36 Johnson et al. (2008) also list coastal-based issues including the alteration of freshwater systems, agriculture, and
the chemical and physical effects from water intake and discharge facilities. These issues are not enumerated here
because they primarily impact the near-shore environment, and are less relevant to the offshore areas of the Ocean
SAMP. Additionally, Johnson et al. (2008) have listed energy-related activities and dredging and disposal activities
as potentially impacting fish habitat. These activities are discussed further in Chapter 9: Other Future Uses.
37 It should be noted that a stock can be overfished with overfishing not occurring, or conversely, overfishing can
occur on a stock that has not yet been found to be overfished.
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as smaller species may proliferate when their predators are reduced through fishing
pressure (Piet and Jennings 2005). In Narragansett Bay and in at least some parts of the
Ocean SAMP area, it has been demonstrated that the species composition has shifted
from one dominated by benthic fish species to one dominated by pelagic fish and benthic
invertebrates, in part because of the impact of fishing on benthic fish species (Collie et al.
2008). See Chapter 2, Ecology of the Ocean SAMP Region for further discussion of this
shift.
4. Bycatch, including the incidental and regulatory discard of species in commercial and
recreational fisheries, can negatively alter the species composition inhabiting the
ecosystems of the Ocean SAMP area, and additionally is a waste of valuable fisheries
resources.
5. Fishing activity can also impact fish habitat, particularly through the use of bottom
fishing gear. Trawls and dredges physically damage the sediment surface, and a large
portion of the epifaunal species living there (such as sponges, corals, and tube worms)
are damaged or removed (Olsgard et al. 2008). Collie et al. (2000) found that one
trawling pass may reduce the abundance of fauna by as much as 55%. These benthic
communities provide habitat for other species, as well as providing food for fish species
and shelter for juveniles (Collie et al. 2004). This loss of habitat complexity may have
important consequences for fish species (Collie et al. 2000). Bottom fishing may also
reduce the abundance of prey species important to commercially and recreationally
important fish species. The particular effects, both initial and long-term, will depend on
the sediment type, the sensitivity of benthic organisms to disturbance, the level of natural
disturbance, and the type of fishing gear being used. The impact of trawling will be
higher at locations that experience low levels of natural disturbance, such as sites in
deeper water, than those areas frequently subject to natural disturbance such as wave
action (Hiddink et al. 2006). Some soft-sediment habitats, such as sand and mud, may be
able to recover fully within a year, while other bottom types may take longer (Collie et
al. 2004). Intensively fished areas may remain in a permanently altered state (Collie et al.
2000). Some areas are trawled repeatedly; the initial impact of trawling on pristine
habitat will be much larger than further trawling activity in previously fished areas
(Hiddink et al. 2006). Areas that are frequently trawled may be dominated by small-
bodied, opportunistic species (Olsgard et al. 2008), as they can withstand higher rates of
mortality, as opposed to large invertebrates, whose abundance may be reduced through
trawling disturbance because of their slow life history (Hiddink et al. 2008). This loss of
large invertebrates may lead to a loss of local biodiversity (Hiddink et al. 2006).
Trawling may have some positive secondary effects for fish species that primarily feed
on small invertebrates by increasing food production of these species; this does not
necessarily mean the net effects of trawling are positive for these species, however,
because of the undesirable ecosystem-level effects (Hiddink et al. 2008). These impacts
to habitat can have secondary effects on fish stocks and on the ecosystem as a whole.
6. Overall, there is a lack of adequate methods to assess trawling impacts at the fishery
scale, and the problem has not been addressed at an ecosystem level. These impacts to
habitat can have secondary effects on fish stocks and on the ecosystem as a whole. To
address this problem, the New England Fishery Management Council is in the process of
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developing an Omnibus Habitat Amendment that will address the effects of fishing on
Essential Fish habitat. The Council is also in the process of developing the Swept Area
Seabed Impact (SASI) Model. The model includes ten different categories of fishing
gear, and will be used to quantitatively assess the effects of fishing to Essential Fish
Habitat. The SASI model may be available for use sometime in 2011 (Bachman pers.
comm.).
550.2. Coastal Development
1. Threats to fish habitat in the Ocean SAMP area from coastal development primarily
result from the discharge of nonpoint source pollution and urban runoff, and specifically
the introduction of pathogens, petroleum products, heavy metals, pesticides, and other
pollutants that can affect marine organisms, even in offshore environments. These
pollutants may sometimes have direct toxic effects on fish, but are more likely to have
sublethal effects that may inhibit the development and reproduction of marine organisms.
Metals, for example, including mercury, lead, copper, and cadmium, can be lethal to fish
at high concentrations, and may also produce effects such as reduced hatch rates of eggs,
increased larval mortality, developmental problems in larvae, and endocrine disruption.
While many of these problems may not have a significant effect on many marine
organisms, metals as well as other compounds bioaccumulate, moving up the food chain
through trophic levels resulting in higher and more damaging concentrations in top
predators, as well as causing health problems in human consumers of fish (Johnson et al.
2008).
2. Eutrophication resulting from nutrient loading can also be a threat, particularly to the
inshore portions of the Ocean SAMP area. These threats can also impact sensitive
estuarine nursery and spawning areas, including Narragansett Bay, of the fish species
found in the Ocean SAMP area (Johnson et al. 2008).
550.3. Introduced Species
1. The introduction of nonnative species is another threat to fish and fish habitat. Introduced
species may include finfish, shellfish, plankton, bacteria, viruses, and pathogens.
Introduced species can cause alterations to habitat, species communities, species
diversity, and food webs, as well as introducing diseases, affecting the health of native
species, and affecting water quality. For example, the green crab, one of the most
common crustaceans in New England waters, is an introduced species from Europe that
grazes on submerged aquatic vegetation and preys on newly settled winter flounder.
Didemnum is an invasive tunicate that has colonized parts of Georges Bank as well as
many coastal areas in New England. This benthic filter-feeder forms dense mats along
the seafloor that prevent the settlement of other benthic organisms, smother benthic
organisms beneath it, and reduce food availability for juvenile scallops and groundfish.
Didemnum also has the ability to change the benthic community structure; it has been
observed to transform heterogeneous gravel habitat into a homogeneous tunicate mat,
reducing important habitat for species such as cod, haddock, and scallops. The changes to
the benthic habitat that occur from bottom trawling and scallop dredging are likely to
contribute to the spread of Didemnum (Lengyel et al. 2009). Nonnative species are likely
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to be introduced through the ballast water of ships coming into or passing through the
area from elsewhere, or through aquaculture operations (Johnson et al. 2008).
2. Introduced species are discussed in more detail in Chapter 2, Ecology of the Ocean
SAMP Region.
550.4. Marine Transportation
1. There is a great deal of commercial shipping through the Ocean SAMP area, and this
activity may have a variety of impacts on fisheries resources. Commercial shipping may
create habitat disturbances by disturbing sediment when operating close to shore, in
shallow waters, or when anchoring. It may also increase underwater noise, which may
affect some fish species (see Chapter 8, Renewable Energy and Other Offshore
Development for further discussion). Vessel operations may also increase the likelihood
that invasive species or pollutants, such as petroleum products, are introduced into the
environment. Much of the Ocean SAMP area shipping traffic involves the movement of
petroleum products. While oil spills are infrequent, such spills can have a major impact
on marine species and on habitat. These impacts can disrupt benthic community
composition and oil can persist in sediments for years after a spill. In addition, the noise
generated by commercial ship traffic can adversely affect fishery resources, impacting
fish spawning, migration, and recruitment behaviors (Johnson et al. 2008). In January
1996, the North Cape barge ran aground off South Kingstown, in the Ocean SAMP area,
and spilled approximately 828,000 gallons of home heating oil into Block Island Sound
and the South County coastal salt ponds. The result was a significant loss of lobster,
finfish, surf clams, seabirds, and other species, and significant impacts on the commercial
fishing and lobstering as well as recreational fishing industries in the state (NOAA
General Counsel for Natural Resources 2010). See Chapter 7, Marine Transportation,
Navigation, and Infrastructure for further discussion.
550.5. Dredged Material Disposal
1. The disposal of dredged materials offshore involves environmental effects beyond those
produced in the dredging process. The U.S. Army Corps of Engineers disposes
approximately 65% of its dredged materials in open waters. For dredged material to be
disposed of offshore, it must be demonstrated that the sediment is compatible with the
sediment at the disposal site, and that the disposal will not disrupt the benthic habitat or
communities (Johnson et al. 2008). Yet the disposal of dredged material can still have a
significant impact. Benthic organisms may be buried in the process, and more mobile
species may leave the area. Recolonization may increase the occurrence of opportunistic
species. These processes may affect fish by reducing prey availability. Dumping may
change the biological and chemical characteristics of the sediment, and will temporarily
increase the turbidity of the water column. The increased volume of suspended sediments
is likely to push some fish out of the area, may affect foraging patterns, and can even
cause injury or death. Sedimentation may also affect the viability of fish eggs and larvae.
On the other hand, some species, including lobster and winter flounder, have been found
to be attracted to dredge disposal sites (Johnson et al. 2008). The disposal of dredged
material can also result in a release of contaminants, making contaminants biologically
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available to organisms in the water column or through the food chain. However, this is
only likely to occur in trace amounts, as generally the disposal of toxic materials through
offshore dumping is prohibited (Johnson et al. 2008).
550.6. Marine Debris
1. Marine debris is an issue in the Ocean SAMP area as it is in the rest of the world’s
oceans. Marine debris may be anything accidentally or intentionally discarded that makes
its way into the ocean, and can include various types of plastics, such as bags, bottles, or
fishing gear. One of the major impacts from marine debris is the entanglement of marine
wildlife, including fish, causing injury or death. A particularly relevant problem for the
Ocean SAMP area may also be the impact of ghost gear, or lost or abandoned fishing
gear, that continues to catch fish long after it has been lost. Marine debris, including
ghost gear, can also damage benthic habitats.
550.7. Marine Fisheries Diseases
1. Marine diseases, including lobster shell disease and mycobacteriosis in striped bass, are
another factor affecting fisheries resources within the Ocean SAMP area. Marine diseases
are discussed further in Chapter 2, Ecology of the Ocean SAMP Region.
550.8. Global Climate Change
1. Global climate change is having, and will likely continue to have, significant impacts on
fisheries resources. Temperature changes can affect the location and timing of spawning,
as well as the timing of plankton blooms and the availability of food, which in turn can
impact the growth and survival of commercially important fish species. The warming
water temperatures are also likely to cause shifts in distribution, with species moving
further north or into deeper waters. Some species important to Rhode Island commercial
fisheries, such as cod and lobster, may shift their range out of the Ocean SAMP area,
while other species found more typically to the south may become more abundant off
Rhode Island. See Chapter 3, Global Climate Change for further discussion.
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Section 560. Policies and Standards
560.1. General Policies
1. The commercial and recreational fishing industries, and the habitats and biological
resources of the ecosystem they are based on, are of vital economic, social, and cultural
importance to Rhode Island’s fishing ports and communities. Commercial and
recreational fisheries are also of great importance to Rhode Island’s economy and to the
quality of life experienced by both residents and visitors. The Council finds that other
uses of the SAMP area could potentially displace commercial or recreational fishing
activities or have other adverse impacts on commercial and recreational fisheries.
2. The Council recognizes that finfish, shellfish, and crustacean resources and related
fishing activities are managed by a host of different agencies and regulatory bodies which
have jurisdiction over different species and/or different parts of the SAMP area. Entities
involved in managing fish and fisheries within the SAMP area include, but are not
limited to, the Atlantic States Marine Fisheries Commission, the RI Department of
Environmental Management, the RI Marine Fisheries Council, the NOAA National
Marine Fisheries Service, the New England Fishery Management Council, and the Mid-
Atlantic Fishery Management Council. The Council recognizes the jurisdiction of these
organizations in fishery management and will work with these entities to protect fisheries
resources. The Council will also work in coordination with these entities to protect
priority habitat areas.
3. The Council’s policy is to protect commercial and recreational fisheries within the SAMP
area from the adverse impacts of other uses, while supporting actions to make ongoing
fishing practices more sustainable. It should be recognized that scientific knowledge of the
impacts of fishing on habitats and fish populations will advance. Improvements in more
sustainable gear technology, fishing practices, and management tools may improve the
state of fisheries resources. A general goal of the Council is to constantly improve the
health of the Ocean SAMP area ecosystem and the populations of fish and shellfish it
provides. Cooperative research, utilizing the unique skills and expertise of the fishing
community, will be a cornerstone to this goal.
4. Commercial and recreational fisheries activities are dynamic, taking place at different
places at different times of the year due to seasonal species migrations and other factors.
The Council recognizes that fisheries are dynamic, shaped by these seasonal migrations
as well as other factors including shifts in the regulatory environment, market demand,
and global climate change. The Council further recognizes that the entire Ocean SAMP
area is used by commercial and recreational fishermen employing different fishing
methods and gear types. Changes in existing uses, intensification of uses, and new uses
within the area could cause adverse impacts to these fisheries. Accordingly, the Council
shall:
i. In consultation with the Fishermen’s Advisory Board, as defined in section
560.2.1, identify and evaluate prime fishing areas on an ongoing basis through an
adaptive framework.
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ii. Review any uses or activities that could disrupt commercial and recreational
fisheries activities.
5. The Council shall work together with the U.S. Coast Guard, the U.S. Navy, the U.S.
Army Corps of Engineers, NOAA, fishermen’s organizations, marine pilots, recreational
boating organizations, and other marine safety organizations to promote safe navigation,
fishing, and recreational boating activity around and through offshore structures and
developments, and along cable routes, during the construction, operation, and
decommissioning phases of such projects. The Council will promote and support the
education of all mariners regarding safe navigation around offshore structures and
developments and along cable routes.
6.
Discussions with the U.S. Coast Guard, the U.S. Department of Interior Bureau of Ocean
Energy Management, Regulation, and Enforcement, and the U.S. Army Corps of
Engineers have indicated that no vessel access restrictions are planned for the waters
around and through offshore structures and developments, or along cable routes, except
for those necessary for navigational safety. Commercial and recreational fishing and
boating access around and through offshore structures and developments and along cable
routes is a critical means of mitigating the potential adverse impacts of offshore
structures on commercial and recreational fisheries and recreational boating. The Council
endorses this approach and shall work to ensure that the waters surrounding offshore
structures, developments, and cable routes remain open to commercial and recreational
fishing, marine transportation, and recreational boating, except for navigational safety
restrictions. The Council requests that federal agencies notify the Council as soon as is
practicable of any federal action that may affect vessel access around and through
offshore structures and developments and along cable routes. The Council will continue
to monitor changes to navigational activities around and through offshore developments
and along cable routes. Any changes affecting existing navigational activities may be
subject to CZMA Federal Consistency review if the federal agency determines its activity
will have reasonably foreseeable effects on the uses or resources of Rhode Island’s
coastal zone.
7. The Council recognizes that commercial and recreational fishermen from other states,
such as the neighboring states of Connecticut, New York, and Massachusetts, often fish
in the Ocean SAMP area. The Council also recognizes that many fish species that are
harvested in adjacent waters may rely on habitats and prey located within the Ocean
SAMP area. Accordingly, the Council will work with neighboring states to ensure that
Offshore Development and other uses of the Ocean SAMP area do not result in
significant impacts to the fisheries resources or activities of other states.
8. The Council shall appoint a standing Fishermen’s Advisory Board (FAB) which shall
provide advice to the Council on the siting and construction of other uses in marine
waters. The FAB is an advisory body to the Council that is not intended to supplant any
existing authority of any other federal or state agency responsible for the management of
fisheries, including but not limited to the Marine Fisheries Council and its authorities set
forth in R.I.G.L. 20-3-1 et seq. The FAB shall be comprised of up to eighteen (18) total
members, to include the following: up to two (2) members representing each of the
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following six Rhode Island fisheries: bottom trawling; scallop dredging; gillnetting;
lobstering; party and charter boat fishing; and recreational angling; and up to six (6)
members, who are Massachusetts fishermen who fish in the Ocean SAMP area to include
four commercial fishermen and two recreational fisherman. When there are two members
representing a fishing interest, only one vote may be cast on behalf of that interest. If the
two members representing that fishery cannot agree on their vote then there shall be no
vote for that fishery for the item under consideration. In any vote on a matter, there shall
be no more than 6 votes total for RI interests and no more than 3 votes total for MA
interests. The FAB members may elect a chair and a vice-chair from amongst its
members. In addition the FAB may establish rules governing its members such as a
minimum number of meetings each member must attend to maintain standing as a
member. FAB members shall serve four-year terms and shall serve no more than two
consecutive terms. The Council shall provide to the FAB a semi-annual status report on
Ocean SAMP area fisheries related issues, including but not limited to those of which the
Council is cognizant in its planning and regulatory activities, and shall notify the FAB in
writing concerning any project in the Ocean SAMP area. The FAB shall meet not less
than semi-annually with the Habitat Advisory Board and on an as-needed basis to
provide the Council with advice on the potential adverse impacts of other uses on
commercial and recreational fishermen and fisheries activities, and on issues including,
but not limited to, the evaluation and planning of project locations, arrangements, and
alternatives; micro-siting (siting of individual wind turbines within a wind farm to
identify the best site for each individual structure); access limitations; and measures to
mitigate the potential impacts of such projects on the fishery. In addition the FAB may
aid the Council and its staff in developing and implementing a research agenda. As new
information becomes available and the scientific understanding of the Ocean SAMP
planning area evolves, the FAB may identify new areas with unique or fragile physical
features, important natural habitats, or areas of high natural productivity for designation
by the Council as Areas of Particular Concern or Areas Designated for Preservation.
560.2. Regulatory Standards
1. Any Large-Scale Offshore Development, as defined in section 1160.1.1, shall require a
meeting between the Fisherman’s Advisory Board (FAB), the applicant, and the Council
staff to discuss potential fishery-related impacts, such as, but not limited to, project
location, construction schedules, alternative locations, project minimization and
identification of high fishing activity or habitat edges. For any state permit process for a
Large-Scale Offshore Development this meeting shall occur prior to submission of the
state permit application. The Council cannot require a pre-application meeting for federal
permit applications, but the Council strongly encourages applicants for any Large-Scale
Offshore Development, as defined in Section 1160.1.1, in federal waters to meet with the
FAB and the Council staff prior to the submission of a federal application, lease, license,
or authorization. However, for federal permit applicants, a meeting with the FAB shall be
necessary data and information required for federal consistency reviews for purposes of
starting the CZMA 6-month review period for federal license or permit activities under
15 C.F.R. part 930, subpart D, and OCS Plans under 15 C.F.R. part 930, subpart E,
pursuant to 15 C.F.R. § 930.58(a)(2). Any necessary data and information shall be
provided before the 6-month CZMA review period begins for a proposed project.
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2. The Council shall prohibit any other uses or activities that would result in significant
long-term negative impacts to Rhode Island’s commercial or recreational fisheries. Long-
term impacts are defined as those that affect more than one or two seasons.
3. The Council shall require that the potential adverse impacts of Offshore Developments
and other uses on commercial or recreational fisheries be evaluated, considered, and
mitigated as described in section 560.2.4.
4. For the purposes of Sections 560.1-560.2, mitigation is defined as a process to make
whole those fisheries user groups that are adversely affected by proposals to be
undertaken, or undertaken projects, in the Ocean SAMP area. Mitigation measures shall
be in consonance with the purposes of duly adopted fisheries management plans,
programs, strategies and regulations of the agencies and regulatory bodies with
jurisdiction over fisheries in the SAMP area, including but not limited to those set forth
above in 560.1.2. Mitigation shall not be designed or implemented in a manner that
substantially diminishes the effectiveness of duly adopted fisheries management
programs. Mitigation measures may include, but are not limited to, compensation, effort
reduction, habitat preservation, restoration
and construction,
marketing, and
infrastructure improvements. Where there are potential impacts associated with proposed
projects, the need for mitigation shall be presumed. Negotiation of mitigation agreements
shall be a necessary condition of any approval or permit of a project by the Council.
Mitigation shall be negotiated between the Council staff, the FAB, the project developer,
and approved by the Council. The reasonable costs associated with the negotiation,
which may include data collection and analysis, technical and financial analysis, and
legal costs, shall be borne by the applicant. The applicant shall establish and maintain
either an escrow account to cover said costs of this negotiation or such other mechanism
as set forth in the permit or approval condition pertaining to mitigation. This policy shall
apply to all Large-Scale Offshore Developments, underwater cables, and other projects
as determined by the Council.
5. Glacial moraines are important habitat areas for a diversity of fish and other marine
plants and animals because of their relative structural permanence and structural
complexity. Glacial moraines create a unique bottom topography that allows for habitat
diversity and complexity, which allows for species diversity in these areas and creates
environments that exhibit some of the highest biodiversity within the entire Ocean SAMP
area. The Council also recognizes that because glacial moraines contain valuable habitats
for fish and other marine life, they are also important to commercial and recreational
fishermen. Accordingly, the Council shall designate glacial moraines as identified in
Chapter 11, Figures 11.3 and 11.4, as Areas of Particular Concern. For further
information on Areas of Particular Concern see Chapter 11, The Policies of the Ocean
SAMP.
6. The Council recognizes that moraine edges, as illustrated in Figure 11.3 and Figure 11.4
in Chapter 11, The Policies of the Ocean SAMP, are important to fishermen. In addition
to these mapped areas, the FAB may identify other edge areas that are important to
fisheries within a proposed project location. The Council shall consider the potential
adverse impacts of future activities or projects on these areas to Rhode Island’s
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commercial and recreational fisheries. Where it is determined that there is a significant
adverse impact, the Council will modify or deny activities that would impact these areas.
In addition, the Council will require assent holders for Offshore Developments to employ
micro-siting techniques in order to minimize the potential impacts of such projects on
these edge areas.
7. The finfish, shellfish, and crustacean species that are targeted by commercial and
recreational fishermen rely on appropriate habitat at all stages of their life cycles. While
all fish habitat is important, spawning and nursery areas are especially important in
providing shelter for these species during the most vulnerable stages of their life cycles.
The Council shall protect sensitive habitats where they have been identified through the
Site Assessment Plan or Construction and Operation Plan review processes for Offshore
Developments as described in Section 1160.5 in Chapter 11, The Policies of the Ocean
SAMP.
8. The Council shall consult with the U.S. Coast Guard, the U.S. Navy, marine pilots, the
FAB, fishermen’s organizations, and recreational boating organizations when scheduling
offshore marine construction or dredging activities. Where it is determined there is a
significant conflict with season-limited commercial or recreational fisheries activities,
recreational boating activities or scheduled events, or other navigation uses, the Council
shall modify or deny activities to minimize conflict with these uses.
9. The Council shall require the assent holder to provide for communication with
commercial and recreational fishermen, mariners, and recreational boaters regarding
offshore marine construction or dredging activities. Communication shall be facilitated
through a project website and shall complement standard U.S. Coast Guard procedures
such as Notices to Mariners for notifying mariners of obstructions to navigation.
10. For all Large-Scale Offshore Developments, underwater cables, and other development
projects as determined by the Council, the assent holder shall designate and fund a third-
party fisheries liaison. The fisheries liaison must be knowledgeable about fisheries and
shall facilitate direct communication between commercial and recreational fishermen and
the project developer. Commercial and recreational fishermen shall have regular contact
with and direct access to the fisheries liaison throughout all stages of an offshore
development (pre-construction; construction; operation; and decommissioning).
11. Where possible, Offshore Developments should be designed in a configuration to
minimize adverse impacts on other user groups, which include but are not limited to:
recreational boaters and fishermen, commercial fishermen, commercial ship operators, or
other vessel operators in the project area. Configurations which may minimize adverse
impacts on vessel traffic include, but are not limited to, the incorporation of a traffic lane
through a development to facilitate safe and direct navigation through, rather than
around, an Offshore Development.
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12. The items listed below shall be required for all Offshore Developments:
i. A biological assessment of commercially and recreationally targeted species shall
be required within the project area for all Offshore Developments. This
assessment shall assess the relative abundance, distribution, and different life
stages of these species at all four seasons of the year. This assessment shall
comprise a series of surveys, employing survey equipment and methods that are
appropriate for sampling finfish, shellfish, and crustacean species at the project’s
proposed location. Such an assessment shall be performed at least four times:
pre-construction (to assess baseline conditions); during construction; and at two
different intervals during operation (i.e. 1 year after construction and then post-
construction). At each time this assessment must capture all four seasons of the
year. This assessment may include evaluation of survey data collected through an
existing survey program, if data are available for the proposed site. The Council
will not require this assessment for proposed projects within the Renewable
Energy Zone that are proposed within two years of the adoption of the Ocean
SAMP.
ii. An assessment of commercial and recreational fisheries effort, landings, and
landings value shall be required for all Offshore Developments. Assessment shall
focus on the proposed project area and alternatives. This assessment shall
evaluate commercial and recreational fishing effort, landings, and landings value
at three different stages: pre-construction (to assess baseline conditions); during
construction; and during operation. At each stage, all four seasons of the year
must be evaluated. Assessment may use existing fisheries monitoring data but
shall be supplemented by interviews with commercial and recreational fishermen.
Assessment shall address whether fishing effort, landings, and landings value has
changed in comparison to baseline conditions. The Council will not require this
assessment for proposed projects within the Renewable Energy Zone that are
proposed within 2 years of the adoption of the Ocean SAMP.
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