Fish and Fisheries in Estuaries. Группа авторов

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of estuary‐associated fishes depend on reproductive success. Estuaries, more than other marine ecosystems, are under threat globally from human and natural perturbations. Amongst the prominent threats to reproduction are effects of heavy fishing on stock abundances, impoundments that limit spawning access and connectivity in anadromous fishes, declines in freshwater discharge that are critical to larval‐stage productivity and cueing, urbanisation, climate‐related increases in temperature that may exceed thermal optima or thresholds for young fishes, effects of contaminants and effects of excessive nutrient pollution (eutrophication) that have led to global rises in harmful algal blooms and hypoxia and, thus, alterations in water quality that limit production of young fish. Catastrophic events, especially those owing to human activity in the estuary and watershed, e.g. hydrocarbon spills or massive toxicant releases, are increasingly noted in estuaries and are threats to the sustainability and dependability of reproduction by estuary‐associated fishes.

      Thanks are extended to the co‐editors of this volume for encouragement and helpful recommendations. The authors acknowledge their respective institutions for facilities support and for providing dependable online access to library resources. Many field assistants made valuable contributions to research conducted by the authors and cited in this chapter; their names are too numerous to mention. The funders, both governmental and non‐governmental, are thanked for their support of research cited in this chapter. Individual funding agencies are acknowledged in cited papers.

      1 Able, K.W. 1978. Ichthyoplankton of the St Lawrence estuary: composition, distribution, and abundance. Journal of the Fisheries Research Board of Canada 35, 1518–1531.

      2 Able, K.W. 2005. A re‐examination of fish estuarine dependence: evidence for connectivity between estuarine and ocean habitats. Estuarine, Coastal and Shelf Science 64, 5–17.

      3 Able, K.W. & Duffy‐Anderson, J.T. 2006. Impacts of piers on juvenile fishes and selected invertebrates in the lower Hudson River. In: The Hudson River (ed., Levinton, J. & Hiles, C. ), pp. 429–440. Cambridge University Press, New York.

      4 Able, K.W. & Fahay, M.P. 1998. The First Year in the Life of Estuarine Fishes in the Middle Atlantic Bight. Rutgers University Press, New Brunswick, NJ.

      5 Able, K.W. & Fahay, M.P. 2010. Ecology of Estuarine Fishes: Temperate Waters of the Western North Atlantic. Johns Hopkins University Press, Baltimore, MD.

      6 Able, K.W., Fahay, M.P. & Shepherd, G.R. 1995. Early life history of black sea bass Centropristis striata in the Mid‐Atlantic Bight and a New Jersey estuary. Fishery Bulletin U.S. 93, 429–445.

      7 Able, K.W., Fahay, M.P., Witting, D.A., et al. 2006. Fish settlement in the ocean versus estuary: comparison of pelagic larval and settled juvenile composition and abundance from southern New Jersey, USA. Estuarine, Coastal and Shelf Science 66, 280–290.

      8 Able, K.W. & Grothues, T.M. 2018. Essential fish habitat for nearshore sentinel species of fishes and crabs in heavily urbanized New York Harbor. Urban Naturalist 16, 1–25.

      9 Able, K. W., Grothues, T.M., Morson, J.M., et al. 2014. Temporal variation in winter flounder recruitment at the southern margin of their range: is the decline due to increasing temperatures? J. Hjort Memorial Issue, ICES Journal of Marine Science 71, 2186–2191.Able, K.W., Grothues, T.M., Shaw, M.J., et al. 2020. Alewife (Alosa pseudoharengus) spawning and nursery areas in a sentinel estuary: Spatial and temporal patterns. Environmental Biology of Fishes 103, 1419–1436.

      10 Able, K.W., Hagan, S.M. & Brown, S.A. 2003. Mechanisms of marsh habitat alteration due to Phragmites: response of young‐of‐the‐year mummichog (Fundulus heteroclitus) to treatment for Phragmites removal. Estuaries 26(2B), 484–494.

      11 Able, K.W., Hagan, S.M., Kovitvongsa, K., et al. 2007. Piscivory by the mummichog Fundulus heteroclitus: evidence from the laboratory and salt marshes. Journal of Experimental Marine Biology and Ecology 345, 26–37.

      12 Able, K.W., Lopez‐Duarte, P.C., Fodrie, F.J., et al. 2015. Fish assemblages in Louisiana salt marshes: effects of the Macondo oil spill. Estuaries and Coasts 38, 1385–1398.

      13 Able, K.W., Manderson, J.P. & Studholme, A.L. 1998. The distribution of shallow water juvenile fishes in an urban estuary: the effects of man‐made structures in the lower Hudson River. Estuaries 21, 731–744.

      14 Able, K.W., Manderson, J.P. & Studholme, A.L. 1999. Habitat quality for shallow water fishes in an urban estuary: the effects of manmade structures on growth. Marine Ecology Progress Series 187, 227–235.

      15 Able, K.W., Morson, J.M. & Fox, D.A. 2017. Food habits of large nektonic fishes: trophic linkages in Delaware Bay and the adjacent ocean. Estuaries and Coasts 41, 866–883.

      16 Able, K.W., Simenstad, C.A., Strydom, N.A., et al. 2022. Chapter 4. Habitat use and connectivity. In: Fish and Fisheries in Estuaries: A Global Perspective (ed., Whitfield, A.K., Able, K.W., Blaber, S.J.M., et al.), pp. 188–254. Wiley Blackwell, Oxford, UK.

      17 Acha, E.M. & Macchi, G.J. 2000. Spawning of Brazilian menhaden, Brevoortia aurea, in the Río de la Plata estuary off Argentina and Uruguay. Fishery Bulletin U.S. 98, 227–235.

      18 Adams, A., Wolfe, R.K., Barkowski, N., et al. 2009. Fidelity to spawning grounds by a catadromous fish, Centropomus undecimalis . Marine Ecology Progress Series 389, 213–222.

      19 Akan, C., Tejada‐Martınez, A.E., Grosch, C.E., et al. 2013. Scalar transport in large‐eddy simulation of Langmuir turbulence in shallow water. Continental Shelf Research 55, 1–16.

      20 Allen, D.M. & Barker, D.L. 1990. Interannual variations in larval fish recruitment to estuarine epibenthic habitats. Marine Ecology Progress Series 63, 113–125.

      21 Amorim, E., Ramos, S., Elliott, M., et al. 2016. Immigration and early life stages recruitment of the European flounder (Platichthys flesus) to an estuarine nursery: the influence of environmental factors. Journal of Sea Research 107, 56–66.

      22 Anderson, J.T. 1988. A review of size dependent survival during pre‐recruit stages of fishes in relation to recruitment. Journal of Northwest Atlantic Fisheries Science 8, 55–66.

      23 Andolina, C., Franzoi, P., Jackson, A.L., et al. 2020. Vegetated habitats trophically support early development stages of a marine migrant fish in a coastal lagoon. Estuaries and Coasts 43, 424–437.

      24 Andutta, F.P., Ridd, P.V. & Wolanski, E. 2011. Dynamics of hypersaline coastal waters in the Great Barrier Reef. Estuarine, Coastal and Shelf Science 94, 299–305.

      25 Annis, E.R., Houde, E.D., Harding, L.W. Jr., et al. 2011. Calibration of a bioenergetics model linking primary production to Atlantic menhaden Brevoortia tyrannus growth in Chesapeake Bay. Marine Ecology Progress Series 437, 253–267.

      26 Arai, T., Limbong, D., Otake, T., et al. 1999a. Metamorphosis and inshore migration of tropical eels Anguilla spp. in the Indo‐Pacific. Marine Ecology Progress Series 182, 283–293.

      27 Arai, T., Otake, T., Limbong, D., et al. 1999b. Early life history and recruitment of the tropical eel Anguilla bicolor pacifica as revealed by otolith microstructure and microchemistry. Marine Biology 133, 319–326.

      28 Arai, T., Otake, T. & Tsukamoto, K. 1997. Drastic changes in otolith microstructure and microchemistry accompanying the onset of metamorphosis in the Japanese eel Anguilla japonica . Marine Ecology Progress Series 161, 17–22.

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