Fishery Bulletin

Papers
(The TQCC of Fishery Bulletin is 0. The table below lists those papers that are above that threshold based on CrossRef citation counts [max. 250 papers]. The publications cover those that have been published in the past four years, i.e., from 2021-08-01 to 2025-08-01.)
ArticleCitations
Modeling somatic and otolith growth of the central subpopulation of northern anchovy (Engraulis mordax) by incorporating seasonality: Suppl. table 28
Effects of incomplete sampling and standardization on indices of abundance from a fishery-independent trawl survey off the Atlantic coast of the southeastern United States: Suppl. Fig. 37
Age validation of the northern stock of black sea bass (Centropristis striata) in the Atlantic Ocean5
Evaluation of factors contributing to postrelease mortality of greater amberjack (Seriola dumerili) in the northern Gulf of Mexico with depth and acceleration data from acoustic tags: Suppl. figs. 1-25
Chemical clocks: using otolith geochemistry to enhance estimation of age and growth of white hake (Urophycis tenuis): Suppl. Fig. 24
Using otolith chronologies to identify extrinsic drivers of growth of 2 commercially targeted small pelagic fish species: supplementary table 34
Effects of incomplete sampling and standardization on indices of abundance from a fishery-independent trawl survey off the Atlantic coast of the southeastern United States4
Examining the periodicity of annular deposition of otolith microconstituents as a means of age validation4
Evaluating otolith increment deposition rates in bigeye tuna (Thunnus obesus) and yellowfin tuna (T. albacares) tagged in the Atlantic Ocean: Suppl. Fig. 24
Comparing the localized feeding ecology of black sea bass (Centropristis striata) at natural and artificial reefs: gut content and stable isotope analyses: Supplementary Figure 13
Assessing postrelease mortality in hook-and-line fishing of a large coastal sciaenid, the white seabass (Atractoscion nobilis): Supplementary Tables3
Reproductive potential of red king crab (Paralithodes camtschaticus) across warm and cold stanzas in Bristol Bay in southwestern Alaska: Supplementary Figure3
Chemical clocks: using otolith geochemistry to enhance estimation of age and growth of white hake (Urophycis tenuis): Suppl. Table 13
Randomization method for evaluating the reliability of a recruitment index in an integrated assessment model3
Effect of reduction in spatial survey effort on indices of bottom temperature for the eastern Bering Sea3
Interspecific differences in the vertical distribution patterns of Sebastes inermis and S. ventricosus: suppl. fig. 22
Long-term dynamics of larval and early juvenile spot (Leiostomus xanthurus) off the U.S. East Coast: relating ocean origins, estuarine ingress, and changing environmental conditions2
Development and use of a large, flexible antenna to detect fish implanted with passive integrated transponder tags2
Comparison of model types for prediction of seafloor trawlability in the Gulf of Alaska by using multibeam sonar data2
Distribution of the tiger shark (Galeocerdo cuvier) in the North Atlantic Ocean by season, sex, and life stage, based on tag and recapture data: supp. figs. 1-22
Comparing the localized feeding ecology of black sea bass (Centropristis striata) at natural and artificial reefs: gut content and stable isotope analyses: Supplementary Figure 22
Life history of the spotted moray (Gymnothorax moringa) off the Atlantic coast of the southeastern United States: age, growth, and reproduction2
Evaluating otolith increment deposition rates in bigeye tuna (Thunnus obesus) and yellowfin tuna (T. albacares) tagged in the Atlantic Ocean: Suppl. Fig. 32
Recruitment of juvenile Atlantic sturgeon (Acipenser oxyrinchus oxyrinchus) in the Savannah, Ogeechee, and Satilla Rivers in Georgia: Supplementary table2
Age, growth, maturity, and natural mortality of the smalltooth sawfish (Pristis pectinata) in Florida waters2
Ovarian masculinization and reproductive impairment in 3 species of groundfish in and around the hypoxic zone in the Gulf of Mexico1
Interactions, injuries, and mortalities of killer whales (Orcinus orca): observed during fishing operations in Alaska: supplementary table 21
New data on the morphology of the Mekong blind sole (Typhlachirus elongatus) indicating the need for a revision of the genus: supplementary table1
Ecology, life history, and fisheries potential of the flathead lobster (Thenus orientalis) in the Arabian Gulf: suppl. table 21
Comparing the localized feeding ecology of black sea bass (Centropristis striata) at natural and artificial reefs: gut content and stable isotope analyses: Supplementary Table 31
Postrelease survival of undersized swordfish (Xiphias gladius) caught on pelagic longline gear in a U.S. commercial fishery in the western North Atlantic Ocean1
A comparison of 4 primary age-structured stock assessment models used in the United States: suppl. material1
1
Age structure and seasonal movement of Atlantic sturgeon (Acipenser oxyrinchus) aggregating in eastern Long Island Sound and the Connecticut River: Supplementary Figure 41
Population dynamics, relative abundance, and habitat suitability for adult red drum (Sciaenops ocellatus) in nearshore waters of the north-central Gulf of Mexico1
An identification guide to the larvae of lanternfishes (Teleostei: Myctophidae) from the Subtropical Convergence: subfamilies Lampanyctinae and Notolychninae: Suppl. Table1
Age structure and seasonal movement of Atlantic sturgeon (Acipenser oxyrinchus) aggregating in eastern Long Island Sound and the Connecticut River: Supplementary Figure 31
Ecology, life history, and fisheries potential of the flathead lobster (Thenus orientalis) in the Arabian Gulf: suppl. table 11
Comparing the localized feeding ecology of black sea bass (Centropristis striata) at natural and artificial reefs: gut content and stable isotope analyses1
Timing and environmental drivers of spawning migrations of alewife (Alosa pseudoharengus) and blueback herring (A. aestivalis) in rivers of Chesapeake Bay: Supplementary figures 5-61
Age structure and seasonal movement of Atlantic sturgeon (Acipenser oxyrinchus) aggregating in eastern Long Island Sound and the Connecticut River1
Updated reproductive parameters for the tiger shark (Galeocerdo cuvier) in the western North Atlantic Ocean0
Ecology, life history, and fisheries potential of the flathead lobster (Thenus orientalis) in the Arabian Gulf: suppl. table 30
0
Reproductive characteristics for the blue shark (Prionace glauca) in the North Atlantic Ocean: supplementary table 10
Assessing postrelease mortality in hook-and-line fishing of a large coastal sciaenid, the white seabass (Atractoscion nobilis): Supplementary Figure0
Randomization method for evaluating the reliability of a recruitment index in an integrated assessment model: Supplementary Table0
Comparing the localized feeding ecology of black sea bass (Centropristis striata) at natural and artificial reefs: gut content and stable isotope analyses: Supplementary Table 10
Evaluating otolith increment deposition rates in bigeye tuna (Thunnus obesus) and yellowfin tuna (T. albacares) tagged in the Atlantic Ocean: Suppl. Fig. 20
Comparison of a bottom longline survey and a bottom trawl survey for 2 groundfish species in the Gulf of Maine to evaluate habitat-related availability of large fish0
0
Dietary niche overlap and prey consumption for the Steller sea lion (Eumetopias jubatus) and California sea lion (Zalophus californianus) in northwest Washington during 2010-2013: suppl. table 20
0
Population dynamics and relative abundance of and habitat suitability for adult red drum (Sciaenops ocellatus) vulnerable to exploitation in nearshore waters of the north-central Gulf of Mexico: suppl0
Assessment of attraction and avoidance behaviors of fish in response to the proximity of transiting underwater vehicles0
0
Habitat associations and effects of survey expansion on abundance indices and population demographics for 2 deepwater fish species off the Atlantic coast of the southeastern United States0
Postrelease survival of undersized swordfish (Xiphias gladius) caught on pelagic longline gear in a U.S. commercial fishery in the western North Atlantic Ocean: Suppl. Fig. 30
Elasmobranch bycatch of the shrimp trawl fishery along the Pacific coast of Guatemala0
Bayesian estimation of the age and growth of the round stingray (Urobatis halleri) in the Gulf of California in Mexico0
Population dynamics and relative abundance of and habitat suitability for adult red drum (Sciaenops ocellatus) vulnerable to exploitation in nearshore waters of the north-central Gulf of Mexico: suppl0
Interactions, injuries, and mortalities of killer whales (Orcinus orca) observed during fishing operations in Alaska0
An identification guide to the larvae of lanternfishes (Teleostei: Myctophidae) from the Subtropical Convergence: subfamilies Lampanyctinae and Notolychninae0
Climate-driven changes in growth and size at maturity of Gulf of Maine lobster stocks: implications for stock assessment models: Supplementary Table0
Chemical clocks: using otolith geochemistry to enhance estimation of age and growth of white hake (Urophycis tenuis): Suppl. Materials0
Reproductive characteristics for the blue shark (Prionace glauca) in the North Atlantic Ocean: supplementary figure 40
Effects of incomplete sampling and standardization on indices of abundance from a fishery-independent trawl survey off the Atlantic coast of the southeastern United States: Suppl. Fig. 10
Dietary niche overlap and prey consumption for the Steller sea lion (Eumetopias jubatus) and California sea lion (Zalophus californianus) in northwest Washington during 2010-2013: suppl. table 60
Exploring the biotic resistance of the invasive green crab (Carcinus maenas) by examining the diet of North American river otters (Lontra canadensis)0
Functional foraging habits and dietary overlap of yellowfin sole (Limanda aspera) and northern rock sole (Lepidopsetta polyxystra) in a coastal nursery of the Bering Sea0
Evaluation of factors contributing to postrelease mortality of greater amberjack (Seriola dumerili) in the northern Gulf of Mexico with depth and acceleration data from acoustic tags: Suppl. table 20
Consumption of Pacific salmon (Oncorhynchus spp.) by California sea lions (Zalophus californianus) and Steller sea lions (Eumetopias jubatus) in northwest Washington during 2010–2013: supplementary ta0
Validation of methods for aging goosefish (Lophius americanus) based on length-mode progression of a strong cohort0
Using otolith chronologies to identify extrinsic drivers of growth of 2 commercially targeted small pelagic fish species: supplementary table 20
Interactions, injuries, and mortalities of killer whales (Orcinus orca): observed during fishing operations in Alaska: supplementary table 30
Dietary niche overlap and prey consumption for the Steller sea lion (Eumetopias jubatus) and California sea lion (Zalophus californianus) in northwest Washington during 2010-2013: suppl. table 50
Arrival and departure windows of Atlantic sturgeon in Chesapeake Bay in Virginia0
The structure of the larval fish assemblage of Massachusetts Bay in 2008–2012 and 2015–20220
New data on the morphology of the Mekong blind sole (Typhlachirus elongatus) indicating the need for a revision of the genus0
Evaluation of factors contributing to postrelease mortality of greater amberjack (Seriola dumerili) in the northern Gulf of Mexico with depth and acceleration data from acoustic tags: Suppl. table 10
Reducing uncertainty in survey abundance estimates by considering alternative designs and estimators: a case study with 3 species in the Gulf of Alaska: suppl. table0
Interactions, injuries, and mortalities of killer whales (Orcinus orca): observed during fishing operations in Alaska: supplementary table 10
Randomization method for evaluating the reliability of a recruitment index in an integrated assessment model: Supplementary Figure0
Effects of salinity and turbidity on development of bamboo sole (Heteromycteris japonicus)0
Descriptions of post-settlement juveniles of 3 greeneye species, Chlorophthalmus nigromarginatus, C. acutifrons, and C. albatrossis (Teleostei: Chlorophthalmidae), from Japan, with notes on their rapi0
Chemical clocks: using otolith geochemistry to enhance estimation of age and growth of white hake (Urophycis tenuis): Suppl. Table 30
Modeling somatic and otolith growth of the central subpopulation of northern anchovy (Engraulis mordax) by incorporating seasonality: Suppl. table 30
Using DNA metabarcoding to reveal prey diversity in diets of juvenile black sea bass (Centropristis striata) in Long Island Sound in the Northwest Atlantic Ocean0
Habitat associations and effects of survey expansion on abundance indices and population demographics for 2 deepwater fish species off the Atlantic coast of the southeastern United States: Supplementa0
0
Consumption of Pacific salmon (Oncorhynchus spp.) by California sea lions (Zalophus californianus) and Steller sea lions (Eumetopias jubatus) in northwest Washington during 2010–2013: supplementary ta0
Reevaluating fecundity of white perch (Morone americana) in Chesapeake Bay with modern stereological techniques0
Age structure and seasonal movement of Atlantic sturgeon (Acipenser oxyrinchus) aggregating in eastern Long Island Sound and the Connecticut River: Supplementary Figure 20
0
Distribution, abundance, and habitat associations of young of the year of rockfish species (Sebastes spp.) in deep waters along the central coast of California0
0
Chemical clocks: using otolith geochemistry to enhance estimation of age and growth of white hake (Urophycis tenuis): Suppl. Fig. 10
A comparison of 4 primary age-structured stock assessment models used in the United States: suppl. figs. 3-80
A comparison of 4 primary age-structured stock assessment models used in the United States: suppl. table 20
Variation in otolith microchemistry for Lebranche mullet (Mugil liza) in southern Brazil and its potential use in identifying their nursery grounds0
Chemical clocks: using otolith geochemistry to enhance estimation of age and growth of white hake (Urophycis tenuis): Suppl. Table 20
Reproductive characteristics for the blue shark (Prionace glauca) in the North Atlantic Ocean0
Morphology, composition, and deterioration of the embryonic rostral sheath of the smalltooth sawfish (Pristis pectinata)0
A comparison of 4 primary age-structured stock assessment models used in the United States: suppl. table 30
Postrelease survival of undersized swordfish (Xiphias gladius) caught on pelagic longline gear in a U.S. commercial fishery in the western North Atlantic Ocean: Suppl. Fig. 20
Overwinter habitat use of young-of-the-year white sharks (Carcharodon carcharias) off the eastern United States0
Reproductive characteristics for the blue shark (Prionace glauca) in the North Atlantic Ocean: supplementary figs. 1-30
Effects of early-life stage and environmental factors on the freshwater and marine survival of Chinook salmon (Oncorhynchus tshawytscha) in rivers of Southeast Alaska0
Using otolith chronologies to identify extrinsic drivers of growth of 2 commercially targeted small pelagic fish species: supplementary table 10
Reproductive characteristics for the blue shark (Prionace glauca) in the North Atlantic Ocean: supplementary table 20
Ecology, life history, and fisheries potential of the flathead lobster (Thenus orientalis) in the Arabian Gulf: suppl. table 40
Reproductive potential of red king crab (Paralithodes camtschaticus) across warm and cold stanzas in Bristol Bay in southwestern Alaska: Supplementary Table0
Consumption of Pacific salmon (Oncorhynchus spp.) by California sea lions (Zalophus californianus) and Steller sea lions (Eumetopias jubatus) in northwest Washington during 2010–20130
Evaluation of factors contributing to postrelease mortality of greater amberjack (Seriola dumerili) in the northern Gulf of Mexico with depth and acceleration data from acoustic tags: Suppl. table 80
Recruitment of juvenile Atlantic sturgeon (Acipenser oxyrinchus oxyrinchus) in the Savannah, Ogeechee, and Satilla Rivers in Georgia0
Timing and environmental drivers of spawning migrations of alewife (Alosa pseudoharengus) and blueback herring (A. aestivalis) in rivers of Chesapeake Bay: Supplementary tables 7-100
Evaluation of factors contributing to postrelease mortality of greater amberjack (Seriola dumerili) in the northern Gulf of Mexico with depth and acceleration data from acoustic tags: Suppl. table 70
Juvenile yield and adult abundance, genetic diversity and structure, and linkages among marine habitats for goldlined spinefoot (Siganus guttatus) in the coastal waters of Vietnam0
First observation of the use of coral habitat by larval northern rockfish (Sebastes polyspinis) in the western Gulf of Alaska0
Interspecific differences in the vertical distribution patterns of Sebastes inermis and S. ventricosus0
Timing and environmental drivers of spawning migrations of alewife (Alosa pseudoharengus) and blueback herring (A. aestivalis) in rivers of Chesapeake Bay0
0
Modeling somatic and otolith growth of the central subpopulation of northern anchovy (Engraulis mordax) by incorporating seasonality: Suppl. table 10
Ecology, life history, and fisheries potential of the flathead lobster (Thenus orientalis) in the Arabian Gulf: suppl. material0
Distribution of the tiger shark (Galeocerdo cuvier) in the North Atlantic Ocean by season, sex, and life stage, based on tag and recapture data: supp. fig. 40
Characterizing spawning behavior of Greenland halibut (Reinhardtius hippoglossoides) in the eastern Bering Sea and Aleutian Islands0
Age structure and seasonal movement of Atlantic sturgeon (Acipenser oxyrinchus) aggregating in eastern Long Island Sound and the Connecticut River: Supplementary Tables0
Examining the periodicity of annular deposition of otolith microconstituents as a means of age validation: Supplementary table0
Dietary niche overlap and prey consumption for the Steller sea lion (Eumetopias jubatus) and California sea lion (Zalophus californianus) in northwest Washington during 2010-2013: suppl. figs. 1-70
Using otolith chronologies to identify extrinsic drivers of growth of 2 commercially targeted small pelagic fish species0
Quantifying the effects of sample size and species distribution on the precision and accuracy of abundance estimates from bottom-trawl surveys in the Gulf of Alaska: Supplemental Table0
Postrelease survival of undersized swordfish (Xiphias gladius) caught on pelagic longline gear in a U.S. commercial fishery in the western North Atlantic Ocean: Suppl. Fig. 10
Comparison of a bottom longline survey and a bottom trawl survey for 2 groundfish species in the Gulf of Maine to evaluate habitat-related availability of large fish: supplementary table0
Discriminating between high- and low-quality field depletion experiments through simulation analysis0
Effect of reduction in spatial survey effort on indices of bottom temperature for the eastern Bering Sea: Suppl. fig. 20
Characterizing spawning behavior of Greenland halibut (Reinhardtius hippoglossoides) in the eastern Bering Sea and Aleutian Islands: supplementary figs. 3 and 40
High survivorship of sandbar sharks (Carcharhinus plumbeus) following catch and release in a growing land-based fishery in Massachusetts0
The structure of the larval fish assemblage of Massachusetts Bay in 2008–2012 and 2015–2022: Supplementary Tables0
Characterizing spawning behavior of Greenland halibut (Reinhardtius hippoglossoides) in the eastern Bering Sea and Aleutian Islands: supplementary fig. 20
Spatiotemporal catch patterns and population distributions of bigeye Pacific opah (Lampris megalopsis) and smalleye Pacific opah (L. incognitus) in the eastern North Pacific Ocean0
Dietary niche overlap and prey consumption for the Steller sea lion (Eumetopias jubatus) and California sea lion (Zalophus californianus) in northwest Washington during 2010-2013: suppl. table 10
Climate-driven changes in growth and size at maturity of Gulf of Maine lobster stocks: implications for stock assessment models: Supplementary Figure 10
Comparison of larval hammerjaw (Omosudis lowii) (Pisces: Alepisauridae) from 3 oceans0
Timing and environmental drivers of spawning migrations of alewife(Alosa pseudoharengus) and blueback herring (A. aestivalis) in rivers of Chesapeake Bay: Supplementa ry tables 3-60
Characterizing spawning behavior of Greenland halibut (Reinhardtius hippoglossoides) in the eastern Bering Sea and Aleutian Islands: supplementary table0
Evaluation of factors contributing to postrelease mortality of greater amberjack (Seriola dumerili) in the northern Gulf of Mexico with depth and acceleration data from acoustic tags0
Climate-driven changes in growth and size at maturity of Gulf of Maine lobster stocks: implications for stock assessment models: Supplementary Material0
Quantifying the effects of sample size and species distribution on the precision and accuracy of abundance estimates from bottom-trawl surveys in the Gulf of Alaska0
Effect of increasing size on the ability of green crab (Carcinus maenas) to manipulate and eat commercially and ecologically important species in the Pacific Northwest0
Dietary niche overlap and prey consumption for the Steller sea lion (Eumetopias jubatus) and California sea lion (Zalophus californianus) in northwest Washington during 2010-20130
Engineering a prototype for a next-generation stock assessment modeling platform: Supplementary Materials0
Reducing uncertainty in survey abundance estimates by considering alternative designs and estimators: a case study with 3 species in the Gulf of Alaska: suppl. fig. 20
Interspecific differences in the vertical distribution patterns of Sebastes inermis and S. ventricosus: suppl. fig. 10
Timing and environmental drivers of spawning migrations of alewife (Alosa pseudoharengus) and blueback herring (A. aestivalis) in rivers of Chesapeake Bay: Supplementary figure 70
Dietary niche overlap and prey consumption for the Steller sea lion (Eumetopias jubatus) and California sea lion (Zalophus californianus) in northwest Washington during 2010-2013: suppl. table 40
Reducing uncertainty in survey abundance estimates by considering alternative designs and estimators: a case study with 3 species in the Gulf of Alaska: suppl. fig. 10
Evaluating otolith increment deposition rates in bigeye tuna (Thunnus obesus) and yellowfin tuna (T. albacares) tagged in the Atlantic Ocean: Suppl. Fig. 30
Ecology, life history, and fisheries potential of the flathead lobster (Thenus orientalis) in the Arabian Gulf: suppl. fig. 50
Ecology, life history, and fisheries potential of the flathead lobster (Thenus orientalis) in the Arabian Gulf0
Reducing uncertainty in survey abundance estimates by considering alternative designs and estimators: a case study with 3 species in the Gulf of Alaska0
Growth and related traits of the sheepswool sponge (Hippospongia lachne): practical and theoretical considerations0
Chemical clocks: using otolith geochemistry to enhance estimation of age and growth of white hake (Urophycis tenuis)0
Ecology, life history, and fisheries potential of the flathead lobster (Thenus orientalis) in the Arabian Gulf: suppl. fig. 40
Comparing the localized feeding ecology of black sea bass (Centropristis striata) at natural and artificial reefs: gut content and stable isotope analyses: Supplementary Table 20
Assessing postrelease mortality in hook-and-line fishing of a large coastal sciaenid, the white seabass (Atractoscion nobilis)0
Life history differences between 2 anadromous populations of the northern form of the Dolly Varden (Salvelinus malma malma) in Bristol Bay in southwestern Alaska0
Interspecific differences in the vertical distribution patterns of Sebastes inermis and S. ventricosus: suppl. fig. 30
Climate-driven changes in growth and size at maturity of Gulf of Maine lobster stocks: implications for stock assessment models: Suppl. Figs. 2-120
Age structure and seasonal movement of Atlantic sturgeon (Acipenser oxyrinchus) aggregating in eastern Long Island Sound and the Connecticut River: Supplementary Figure 10
Effect of reduction in spatial survey effort on indices of bottom temperature for the eastern Bering Sea: Suppl. fig. 10
Age, growth parameters, and reproductive characteristics of the sharpspine skate (Okamejei acutispina) in the East China Sea0
Characterizing spawning behavior of Greenland halibut (Reinhardtius hippoglossoides) in the eastern Bering Sea and Aleutian Islands: supplementary fig. 10
Collecting age and length data from recovered carcasses of filleted rockfish: a new data source for examination of life history characteristics0
Evaluating otolith increment deposition rates in bigeye tuna (Thunnus obesus) and yellowfin tuna (T. albacares) tagged in the Atlantic Ocean: Suppl. Tables 1-20
Effects of incomplete sampling and standardization on indices of abundance from a fishery-independent trawl survey off the Atlantic coast of the southeastern United States: Suppl. Fig. 20
Effects of incomplete sampling and standardization on indices of abundance from a fishery-independent trawl survey off the Atlantic coast of the southeastern United States: Suppl. table0
0
Functional foraging habits and dietary overlap of yellowfin sole (Limanda aspera) and northern rock sole (Lepidopsetta polyxystra) in a coastal nursery of the Bering Sea: suppl. table0
A comparison of 4 histological staining methods for revealing oocyte development, atresia, and postovulatory follicles in 3 fish species: Supplementary Table0
Spatiotemporal dynamics of dolphinfish (Coryphaena hippurus) in the western Atlantic Ocean: supp. fig. 20
Comparison of a bottom longline survey and a bottom trawl survey for 2 groundfish species in the Gulf of Maine to evaluate habitat-related availability of large fish: supplementary figures 1 and 20
Life history differences between 2 anadromous populations of the northern form of the Dolly Varden (Salvelinus malma malma) in Bristol Bay in southwestern Alaska: Suppl. Table0
Timing and environmental drivers of spawning migrations of alewife(Alosa pseudoharengus) and blueback herring (A. aestivalis) in rivers of Chesapeake Bay: Supplementary table 10
Evaluating otolith increment deposition rates in bigeye tuna (Thunnus obesus) and yellowfin tuna (T. albacares) tagged in the Atlantic Ocean: Suppl. Tables 3-60
Seasonal behavioral changes of a captive whale shark (Rhincodon typus) under variable temperature and light conditions0
Consumption of Pacific salmon (Oncorhynchus spp.) by California sea lions (Zalophus californianus) and Steller sea lions (Eumetopias jubatus) in northwest Washington during 2010–2013: supplementary ta0
Evaluation of factors contributing to postrelease mortality of greater amberjack (Seriola dumerili) in the northern Gulf of Mexico with depth and acceleration data from acoustic tags: Suppl. tables 4-0
Bayesian estimation of the age and growth of the round stingray (Urobatis halleri) in the Gulf of California in Mexico: supplementary table0
Ecology, life history, and fisheries potential of the flathead lobster (Thenus orientalis) in the Arabian Gulf: suppl. figs. 1-20
0
Distribution of the tiger shark (Galeocerdo cuvier) in the North Atlantic Ocean by season, sex, and life stage, based on tag and recapture data0
Timing and environmental drivers of spawning migrations of alewife (Alosa pseudoharengus) and blueback herring (A. aestivalis) in rivers of Chesapeake Bay: Supplementary table 20
Postrelease survival of undersized swordfish (Xiphias gladius) caught on pelagic longline gear in a U.S. commercial fishery in the western North Atlantic Ocean0
Modeling somatic and otolith growth of the central subpopulation of northern anchovy (Engraulis mordax) by incorporating seasonality0
Spatiotemporal dynamics of dolphinfish (Coryphaena hippurus) in the western Atlantic Ocean0
Evaluating otolith increment deposition rates in bigeye tuna (Thunnus obesus) and yellowfin tuna (T. albacares) tagged in the Atlantic Ocean: Suppl. Tables 3-60
High survivorship of sandbar sharks (Carcharhinus plumbeus) following catch and release in a growing land-based fishery in Massachusetts: suppl. fig.0
A comparison of 4 primary age-structured stock assessment models used in the United States: suppl. figs. 1-20
Evaluating otolith increment deposition rates in bigeye tuna (Thunnus obesus) and yellowfin tuna (T. albacares) tagged in the Atlantic Ocean0
Dietary niche overlap and prey consumption for the Steller sea lion (Eumetopias jubatus) and California sea lion (Zalophus californianus) in northwest Washington during 2010-2013: suppl. figs. 8-140
Validation of methods for aging goosefish (Lophius americanus) based on length-mode progression of a strong cohort: supplementary table0
Engineering a prototype for a next-generation stock assessment modeling platform0
Consumption of Pacific salmon (Oncorhynchus spp.) by California sea lions (Zalophus californianus) and Steller sea lions (Eumetopias jubatus) in northwest Washington during 2010–2013: supplementary ta0
Evaluating otolith increment deposition rates in bigeye tuna (Thunnus obesus) and yellowfin tuna (T. albacares) tagged in the Atlantic Ocean: Suppl. Tables 1-20
A comparison of 4 histological staining methods for revealing oocyte development, atresia, and postovulatory follicles in 3 fish species: Supplementary Materials0
Randomization method for evaluating the reliability of a recruitment index in an integrated assessment model: Supplementary Material0
Reproductive potential of red king crab (Paralithodes camtschaticus) across warm and cold stanzas in Bristol Bay in southwestern Alaska0
0
Climate-driven changes in growth and size at maturity of Gulf of Maine lobster stocks: implications for stock assessment models0
A comparison of 4 primary age-structured stock assessment models used in the United States0
Timing and environmental drivers of spawning migrations of alewife (Alosa pseudoharengus) and blueback herring (A. aestivalis) in rivers of Chesapeake Bay: Supplementary figures 1-40
Evaluation of factors contributing to postrelease mortality of greater amberjack (Seriola dumerili) in the northern Gulf of Mexico with depth and acceleration data from acoustic tags: Suppl. table 30
A comparison of 4 primary age-structured stock assessment models used in the United States: suppl. table 10
Characterizing spawning behavior of Greenland halibut (Reinhardtius hippoglossoides) in the eastern Bering Sea and Aleutian Islands: supplementary materials0
High survivorship of sandbar sharks (Carcharhinus plumbeus) following catch and release in a growing land-based fishery in Massachusetts: suppl. table0
Exploring the biotic resistance of the invasive green crab (Carcinus maenas) by examining the diet of North American river otters (Lontra canadensis): suppl. figure0
Mortality estimates for gray triggerfish (Balistes capriscus) in the northern Gulf of Mexico based on acoustic telemetry0
Ecology, life history, and fisheries potential of the flathead lobster (Thenus orientalis) in the Arabian Gulf: suppl. fig. 30
Dietary niche overlap and prey consumption for the Steller sea lion (Eumetopias jubatus) and California sea lion (Zalophus californianus) in northwest Washington during 2010-2013: suppl. table 30
Spatiotemporal dynamics of dolphinfish (Coryphaena hippurus) in the western Atlantic Ocean: supp. fig. 10
Evaluating otolith increment deposition rates in bigeye tuna (Thunnus obesus) and yellowfin tuna (T. albacares) tagged in the Atlantic Ocean: Suppl. Fig. 10
0
Distribution of the tiger shark (Galeocerdo cuvier) in the North Atlantic Ocean by season, sex, and life stage, based on tag and recapture data: supp. fig. 30
0
A comparison of 4 histological staining methods for revealing oocyte development, atresia, and postovulatory follicles in 3 fish species0
Biological characteristics of the primitive flatfish Indian halibut (Psettodes erumei) from the tropical northeastern Indian Ocean, including implications of the use of incorrect aging methods on mort0
Spatiotemporal dynamics of dolphinfish (Coryphaena hippurus) in the western Atlantic Ocean: supp. fig. 30
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