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 2022-08-01 to 2026-08-01.)
ArticleCitations
Assessing postrelease mortality in hook-and-line fishing of a large coastal sciaenid, the white seabass (Atractoscion nobilis): Supplementary Tables9
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. 36
Chemical clocks: using otolith geochemistry to enhance estimation of age and growth of white hake (Urophycis tenuis): Suppl. Fig. 24
Evaluating otolith increment deposition rates in bigeye tuna (Thunnus obesus) and yellowfin tuna (T. albacares) tagged in the Atlantic Ocean: Suppl. Fig. 24
Randomization method for evaluating the reliability of a recruitment index in an integrated assessment model3
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
Condition of larval walleye pollock (Gadus chalcogrammus) in the southeastern Bering Sea in relation to their environment and size: Supplementary Figure 13
Effects of incomplete sampling and standardization on indices of abundance from a fishery-independent trawl survey off the Atlantic coast of the southeastern United States3
Reproductive potential of red king crab (Paralithodes camtschaticus) across warm and cold stanzas in Bristol Bay in southwestern Alaska: Supplementary Figure3
Standardized catch rates of silky sharks (Carcharhinus falciformis) in a commercial longline fishery of the eastern Pacific Ocean: Supplementary Materials2
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
Examining the periodicity of annular deposition of otolith microconstituents as a means of age validation2
Effect of reduction in spatial survey effort on indices of bottom temperature for the eastern Bering Sea2
Evaluating otolith increment deposition rates in bigeye tuna (Thunnus obesus) and yellowfin tuna (T. albacares) tagged in the Atlantic Ocean: Suppl. Fig. 32
Interspecific differences in the vertical distribution patterns of Sebastes inermis and S. ventricosus: suppl. fig. 22
Reemergence of the endangered smalltooth sawfish (Pristis pectinata) in a historical nursery in southeast Florida2
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
Age, growth, maturity, and natural mortality of the smalltooth sawfish (Pristis pectinata) in Florida waters2
Chemical clocks: using otolith geochemistry to enhance estimation of age and growth of white hake (Urophycis tenuis): Suppl. Table 12
Cranial myology of the smalltooth sawfish (Pristis pectinata): implications for headshaking behaviors and entanglement in marine debris1
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
Age structure and seasonal movement of Atlantic sturgeon (Acipenser oxyrinchus) aggregating in eastern Long Island Sound and the Connecticut River: Supplementary Figure 31
Standardized catch rates of silky sharks (Carcharhinus falciformis) in a commercial longline fishery of the eastern Pacific Ocean1
Development and use of a large, flexible antenna to detect fish implanted with passive integrated transponder tags1
Recruitment of juvenile Atlantic sturgeon (Acipenser oxyrinchus oxyrinchus) in the Savannah, Ogeechee, and Satilla Rivers in Georgia: Supplementary table1
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 41
Estuarine diet of North American river otters (Lontra canadensis) in Makah Bay on the Makah Indian Reservation in Washington: Supplementary Tables1
Comparing the localized feeding ecology of black sea bass (Centropristis striata) at natural and artificial reefs: gut content and stable isotope analyses: Supplementary Figure 21
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
Postrelease survival of undersized swordfish (Xiphias gladius) caught on pelagic longline gear in a U.S. commercial fishery in the western North Atlantic Ocean1
Ovarian masculinization and reproductive impairment in 3 species of groundfish in and around the hypoxic zone in the Gulf of Mexico1
Collecting age and length data from recovered carcasses of filleted rockfish: a new data source for examination of life history characteristics0
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Reproductive biology and age at maturity of shortspine thornyhead (Sebastolobus alascanus) in Alaska0
Age structure and seasonal movement of Atlantic sturgeon (Acipenser oxyrinchus) aggregating in eastern Long Island Sound and the Connecticut River: Supplementary Figure 10
Modeling somatic and otolith growth of the central subpopulation of northern anchovy (Engraulis mordax) by incorporating seasonality: Suppl. table 30
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
High survivorship of sandbar sharks (Carcharhinus plumbeus) following catch and release in a growing land-based fishery in Massachusetts: suppl. fig.0
Reducing uncertainty in survey abundance estimates by considering alternative designs and estimators: a case study with 3 species in the Gulf of Alaska0
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
Comparison of larval hammerjaw (Omosudis lowii) (Pisces: Alepisauridae) from 3 oceans0
A description of the gargaropteron stage of Kali macrodon, based on morphological and molecular data, with notes on the taxonomy of the genus0
Estimation of total abundance for adult Atlantic sturgeon (Acipenser oxyrinchus) in the York River in Virginia0
Climate-driven changes in growth and size at maturity of Gulf of Maine lobster stocks: implications for stock assessment models: Supplementary Table0
Exploring the biotic resistance of the invasive green crab (Carcinus maenas) by examining the diet of North American river otters (Lontra canadensis)0
Timing and environmental drivers of spawning migrations of alewife (Alosa pseudoharengus) and blueback herring (A. aestivalis) in rivers of Chesapeake Bay: Supplementary figure 70
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
Spatiotemporal dynamics of dolphinfish (Coryphaena hippurus) in the western Atlantic Ocean0
Engineering a prototype for a next-generation stock assessment modeling platform: Supplementary Materials0
The structure of the larval fish assemblage of Massachusetts Bay in 2008–2012 and 2015–2022: Supplementary Tables0
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
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
Reproductive biology and age at maturity of shortspine thornyhead (Sebastolobus alascanus) in Alaska: Supplementary Figure0
Condition of larval walleye pollock (Gadus chalcogrammus) in the southeastern Bering Sea in relation to their environment and size0
Randomization method for evaluating the reliability of a recruitment index in an integrated assessment model: Supplementary Material0
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
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
Description of eggs, larvae, and early juveniles of southern black drum (Pogonias courbina) reared in captivity0
Effect of reduction in spatial survey effort on indices of bottom temperature for the eastern Bering Sea: Suppl. fig. 20
Elasmobranch bycatch of the shrimp trawl fishery along the Pacific coast of Guatemala0
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
Spatiotemporal dynamics of dolphinfish (Coryphaena hippurus) in the western Atlantic Ocean: supp. fig. 20
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A comparison of 4 histological staining methods for revealing oocyte development, atresia, and postovulatory follicles in 3 fish species: Supplementary Materials0
Reproductive potential of red king crab (Paralithodes camtschaticus) across warm and cold stanzas in Bristol Bay in southwestern Alaska0
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
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
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
Age structure and seasonal movement of Atlantic sturgeon (Acipenser oxyrinchus) aggregating in eastern Long Island Sound and the Connecticut River: Supplementary Tables0
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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 Ocean0
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High survivorship of sandbar sharks (Carcharhinus plumbeus) following catch and release in a growing land-based fishery in Massachusetts: suppl. table0
Climate-driven changes in growth and size at maturity of Gulf of Maine lobster stocks: implications for stock assessment models: Suppl. Figs. 2-120
Chemical clocks: using otolith geochemistry to enhance estimation of age and growth of white hake (Urophycis tenuis)0
Exploring the use of artificial baits to avoid shark capture in a Hawaii-based tuna fishery0
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Comparing the localized feeding ecology of black sea bass (Centropristis striata) at natural and artificial reefs: gut content and stable isotope analyses0
Effects of salinity and turbidity on development of bamboo sole (Heteromycteris japonicus)0
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
Age, growth, and reproduction of the axillary seabream (Pagellus acarne) off the coast of Portugal0
Age structure and seasonal movement of Atlantic sturgeon (Acipenser oxyrinchus) aggregating in eastern Long Island Sound and the Connecticut River: Supplementary Figure 20
The structure of the larval fish assemblage of Massachusetts Bay in 2008–2012 and 2015–20220
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Modeling somatic and otolith growth of the central subpopulation of northern anchovy (Engraulis mordax) by incorporating seasonality: Suppl. table 10
Engineering a prototype for a next-generation stock assessment modeling platform0
Life history differences between 2 anadromous populations of the northern form of the Dolly Varden (Salvelinus malma malma) in Bristol Bay in southwestern Alaska0
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
High survivorship of sandbar sharks (Carcharhinus plumbeus) following catch and release in a growing land-based fishery in Massachusetts0
Chemical clocks: using otolith geochemistry to enhance estimation of age and growth of white hake (Urophycis tenuis): Suppl. Table 30
A comparison of 4 histological staining methods for revealing oocyte development, atresia, and postovulatory follicles in 3 fish species0
Postrelease survival of undersized swordfish (Xiphias gladius) caught on pelagic longline gear in a U.S. commercial fishery in the western North Atlantic Ocean0
Chemical clocks: using otolith geochemistry to enhance estimation of age and growth of white hake (Urophycis tenuis): Suppl. Table 20
Evaluating otolith increment deposition rates in bigeye tuna (Thunnus obesus) and yellowfin tuna (T. albacares) tagged in the Atlantic Ocean: Suppl. Fig. 30
Condition of larval walleye pollock (Gadus chalcogrammus) in the southeastern Bering Sea in relation to their environment and size: Supplementary Figure 30
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: Supplementa ry tables 3-60
Reproductive potential of red king crab (Paralithodes camtschaticus) across warm and cold stanzas in Bristol Bay in southwestern Alaska: Supplementary Table0
Estimation of total abundance for adult Atlantic sturgeon (Acipenser oxyrinchus) in the York River in Virginia0
Evaluating otolith increment deposition rates in bigeye tuna (Thunnus obesus) and yellowfin tuna (T. albacares) tagged in the Atlantic Ocean: Suppl. Fig. 20
Randomization method for evaluating the reliability of a recruitment index in an integrated assessment model: Supplementary Figure0
Evaluating otolith increment deposition rates in bigeye tuna (Thunnus obesus) and yellowfin tuna (T. albacares) tagged in the Atlantic Ocean: Suppl. Tables 1-20
Assessing postrelease mortality in hook-and-line fishing of a large coastal sciaenid, the white seabass (Atractoscion nobilis)0
Exploring the biotic resistance of the invasive green crab (Carcinus maenas) by examining the diet of North American river otters (Lontra canadensis): suppl. figure0
Climate-driven changes in growth and size at maturity of Gulf of Maine lobster stocks: implications for stock assessment models: Supplementary Figure 10
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
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Climate-driven changes in growth and size at maturity of Gulf of Maine lobster stocks: implications for stock assessment models: Supplementary Material0
Recruitment of juvenile Atlantic sturgeon (Acipenser oxyrinchus oxyrinchus) in the Savannah, Ogeechee, and Satilla Rivers in Georgia0
Evaluating otolith increment deposition rates in bigeye tuna (Thunnus obesus) and yellowfin tuna (T. albacares) tagged in the Atlantic Ocean: Suppl. Tables 3-60
Age structure and seasonal movement of Atlantic sturgeon (Acipenser oxyrinchus) aggregating in eastern Long Island Sound and the Connecticut River0
Variation in otolith microchemistry for Lebranche mullet (Mugil liza) in southern Brazil and its potential use in identifying their nursery grounds0
Reproductive biology and age at maturity of shortspine thornyhead (Sebastolobus alascanus) in Alaska: Supplementary Table0
Randomization method for evaluating the reliability of a recruitment index in an integrated assessment model: Supplementary Table0
Assessing postrelease mortality in hook-and-line fishing of a large coastal sciaenid, the white seabass (Atractoscion nobilis): Supplementary Figure0
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
Condition of larval walleye pollock (Gadus chalcogrammus) in the southeastern Bering Sea in relation to their environment and size: Supplementary Figure 30
Chemical clocks: using otolith geochemistry to enhance estimation of age and growth of white hake (Urophycis tenuis): Suppl. Fig. 10
Examining the periodicity of annular deposition of otolith microconstituents as a means of age validation: Supplementary 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. 20
Climate-driven changes in growth and size at maturity of Gulf of Maine lobster stocks: implications for stock assessment models0
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
An identification guide to the larvae of lanternfishes (Teleostei: Myctophidae) from the Subtropical Convergence: subfamilies Lampanyctinae and Notolychninae0
Distribution, abundance, and habitat associations of young of the year of rockfish species (Sebastes spp.) in deep waters along the central coast of California0
Timing and environmental drivers of spawning migrations of alewife (Alosa pseudoharengus) and blueback herring (A. aestivalis) in rivers of Chesapeake Bay: Supplementary table 20
Seasonal behavioral changes of a captive whale shark (Rhincodon typus) under variable temperature and light conditions0
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
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
Estuarine diet of North American river otters (Lontra canadensis) in Makah Bay on the Makah Indian Reservation in Washington0
Condition of larval walleye pollock (Gadus chalcogrammus) in the southeastern Bering Sea in relation to their environment and size: Supplementary Figure 20
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. 10
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
Age, growth parameters, and reproductive characteristics of the sharpspine skate (Okamejei acutispina) in the East China Sea0
Condition of larval walleye pollock (Gadus chalcogrammus) in the southeastern Bering Sea in relation to their environment and size: Supplementary Figure 10
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
Reevaluating fecundity of white perch (Morone americana) in Chesapeake Bay with modern stereological techniques0
Chemical clocks: using otolith geochemistry to enhance estimation of age and growth of white hake (Urophycis tenuis): Suppl. Materials0
Timing and environmental drivers of spawning migrations of alewife (Alosa pseudoharengus) and blueback herring (A. aestivalis) in rivers of Chesapeake Bay0
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
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
Updated reproductive parameters for the tiger shark (Galeocerdo cuvier) in the western North Atlantic Ocean0
Interspecific differences in the vertical distribution patterns of Sebastes inermis and S. ventricosus: suppl. fig. 30
Spatiotemporal dynamics of dolphinfish (Coryphaena hippurus) in the western Atlantic Ocean: supp. fig. 30
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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. Tables 1-20
Interspecific differences in the vertical distribution patterns of Sebastes inermis and S. ventricosus: suppl. fig. 10
Arrival and departure windows of Atlantic sturgeon in Chesapeake Bay in Virginia0
Evaluating otolith increment deposition rates in bigeye tuna (Thunnus obesus) and yellowfin tuna (T. albacares) tagged in the Atlantic Ocean: Suppl. Tables 3-60
Morphology, composition, and deterioration of the embryonic rostral sheath of the smalltooth sawfish (Pristis pectinata)0
A comparison of 4 histological staining methods for revealing oocyte development, atresia, and postovulatory follicles in 3 fish species: Supplementary Table0
Effect of reduction in spatial survey effort on indices of bottom temperature for the eastern Bering Sea: Suppl. fig. 10
Modeling somatic and otolith growth of the central subpopulation of northern anchovy (Engraulis mordax) by incorporating seasonality0
Interspecific differences in the vertical distribution patterns of Sebastes inermis and S. ventricosus0
Condition of larval walleye pollock (Gadus chalcogrammus) in the southeastern Bering Sea in relation to their environment and size: Supplementary Figure 20
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