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Salt Marsh Linkages to Productivity of Penaeid Shrimps and Blue Crabs in the Northern Gulf of Mexico

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Concepts and Controversies in Tidal Marsh Ecology

Abstract

Secondary production derived from coastal marshes of the northern Gulf of Mexico exceeds that of other regions in the United States and is exemplified by large fishery catches of penaeid shrimps (Farfantepenaeus aztecus, F. duorarum, and Litopenaeus setiferus – 66% of U.S.) and blue crabs (Callinectessapidus −25% of U.S.). We believe that this production arises from coastal wetlands, and is driven by wetland geomorphology and hydrology resulting from the delta building and wetland loss cycles of the Mississippi River. Quantitative surveys document that high densities of shrimps and blue crabs directly use northern Gulf marsh surfaces. Manipulative experiments demonstrate that such marshes provide these fishery species with increased resources for growth and with protective cover to reduce predator-related mortality. Thus, access to the marsh surface is an important component in controlling the link between secondary productivity and coastal wetlands. Marsh access is influenced by tidal flooding patterns, amount of marsh/water edge, and extent of connections between marsh systems and the Gulf. Low-elevation Gulf marshes are flooded nearly continually during some seasons and are extensively fragmented; such characteristics provide maximum access. By contrast, U.S. Atlantic coast marshes have less fragmentation and less flooding. These geomorphic and hydrologic differences coincide with differences in secondary production between the regions, e.g., marsh-derived fishery production is lower on the Atlantic coast. Despite the linkage between coastal wetlands and secondary production, the current rapid loss of wetlands in the Gulf does not appear to be causing a decline, but instead is associated with an increase in fishery productivity. This paradox may be explained by changes in access and habitat function during areal loss of wetlands. Wetland loss is accompanied by increased marsh inundation and fragmentation, expansion of saline zones, and shortened migratory routes. These processes extend the utilization of remaining marsh and support temporary increases in secondary production.

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Literature Cited

  • Aldrich, D. V., C. E. Wood and K. N. Baxter. 1968. An ecological interpretation of low temperature responses in Penaeus aztecus and P. setiferus postlarvae. Bulletin of Marine Science 18:61–71.

    Google Scholar 

  • Alexander, S. K. 1986. Diet of the blue crab, Callinectes sapidus Rathbun, from nearshore habitats of Galveston Island, Texas. Texas Journal of Science 38:85–89.

    Google Scholar 

  • Armentano, T. V., R. A. Park and C. L. Cloonan. 1988. Impacts on coastal wetlands throughout the United States. Pages 87–149 in J. G. Titus, editor. Greenhouse effect, sea level rise and coastal wetlands. EPA-230-05-86-013, U.S. EPA, Office of Policy, Planning and Evaluation, Washington, District of Columbia, USA.

    Google Scholar 

  • Baltz, D. M., C. Rakocinski and J. W. Fleeger. 1993. Microhabitat use by marsh-edge fishes in a Louisiana estuary. Environmental Biology of Fishes 36:109–126.

    Google Scholar 

  • Baxter, K. N. and W. C. Renfro. 1967. Seasonal occurrence and size distribution of postlarval brown and white shrimp near Galveston, Texas, with notes on species identification. Fishery Bulletin, U.S. 66:149–158.

    Google Scholar 

  • Boesch, D. F. and R. E. Turner. 1984. Dependence of fishery species on salt marshes: the role of food and refuge. Estuaries 7:460–468.

    Google Scholar 

  • Browder, J. A., H. A. Bartley and K. S. Davis. 1985. A probabilistic model of the relationship between marshland-water interface and marsh disintegration. Ecological Modeling 29:245–260.

    Article  Google Scholar 

  • Browder, J. A., L. N. May, A. Rosenthal, J. G. Gosselink and R. H. Baumann. 1989. Modeling future trends in wetland loss and brown shrimp production in Louisiana using thematic mapper imagery. Remote Sensing of the Environment 28:45–59.

    Article  Google Scholar 

  • Castellanos, D. L. 1997. Nekton use of submerged aquatic vegetation, marsh and shallow unvegetated bottom in a Louisiana tidal freshwater ecosystem. Thesis, University of Southwestern Louisiana, Lafayette, Louisiana, USA.

    Google Scholar 

  • Childers, D. L., J. W. Day and R. A. Muller. 1990. Relating climatological forcing to coastal water levels in Louisiana estuaries and the potential importance of El Nino-Southern Oscillation events. Climate Research 1:31–42.

    Google Scholar 

  • Coen, L. D., K. L. Heck and L. G. Abele. 1981. Experiments on competition and predation among shrimps of seagrass meadows. Ecology 62:1484–1493.

    Google Scholar 

  • Condrey, R. E. and D. Fuller. 1992. The U.S. Gulf shrimp fishery. Pages 89–119 in M. H. Glantz, editor. Climate variability, climate change and fisheries. Cambridge University Press, England.

    Google Scholar 

  • Condrey, R. E., J. G. Gosselink and H. J. Bennett. 1972. Comparison of the assimilation of different diets by Penaeus setiferus and Penaeus aztecus. Fishery Bulletin, U.S. 70:1281–1292.

    CAS  Google Scholar 

  • Conner, W. H. and J. W. Day. 1987. The ecology of Barataria Basin, Louisiana: an estuarine profile. U.S. Fish and Wildlife Service Biological Report 85(7.13).

    Google Scholar 

  • Dahl, T. and C. Johnson. 1991. Wetlands: status and trends in the conterminous United States, mid-1970s to mid-1980s. Report to Congress, U.S. Department of the Interior, Fish and Wildlife Service, Washington, District of Columbia, USA.

    Google Scholar 

  • Dahlberg, M. D. and F. G. Smith. 1970. Mortality of estuarine animals due to cold in the Georgian coast. Ecology 51:931–933.

    Google Scholar 

  • Deegan, L. A. and B. A. Thompson. 1985. The ecology of fish communities in the Mississippi River deltaic plain. Pages 35–56 in A. Yanez-Arancibia, editor. Fish community ecology in estuaries and coastal lagoons: towards an ecosystem integration. UNAM Press, Mexico City, Mexico.

    Google Scholar 

  • DeLaune, R. D., R. H. Baumann and J. G. Gosselink. 1983. Relationships among vertical accretion, coastal submergence and erosion in a Louisiana Gulf coast marsh. Journal of Sedimentary Petrology 53:147–157.

    Google Scholar 

  • DeLaune, R. D., T. C. Feijtel and W. H. Patrick. 1989. Nitrogen flows in Louisiana gulf coast salt marsh: spatial considerations. Biogeochemistry 8:25–37.

    Article  CAS  Google Scholar 

  • DeLaune, R. D., C. J. Smith, W. H. Patrick and H. H. Roberts. 1987. Rejuvenated marsh and bay-bottom accretion on the rapidly subsiding coastal plain of the U.S. Gulf coast: a second order effect of the emerging Atchafalaya Delta. Estuarine, Coastal and Shelf Science 25:381–389.

    CAS  Google Scholar 

  • Dittel, A. I., A. H. Hines, G. M. Ruiz and K. K. Ruffin. 1995. Effects of shallow water refuge on behavior and density-dependent mortality of juvenile blue crabs in Chesapeake Bay. Bulletin of Marine Science 57:902–916.

    Google Scholar 

  • Eldred, B., R. M. Ingle, K. D. Woodburn, R. F. Hutton and H. Jones. 1961. Biological observations on the commercial shrimp, Penaeus duorarum Burkenroad, in Florida waters. Florida State Board of Conservation, Professional Paper Series 3:1–139.

    Google Scholar 

  • Eldridge, P. J. 1988. The southeast area monitoring and assessment program (SEAMAP): a state-federal-university program for collection, management and dissemination of fishery-independent data and information in the southeastern United States. Marine Fisheries Review 50:29–39.

    Google Scholar 

  • Feijtel, T. C., R. D. DeLaune and W. H. Patrick. 1985. Carbon flow in coastal Louisiana. Marine Ecology Progress Series 24:255–260.

    CAS  Google Scholar 

  • Fitz, H. C. and R. G. Wiegert. 1991. Utilization of the intertidal zone of a salt marsh by the blue crab Callinectes sapidus–density, return frequency and feeding habits. Marine Ecology Progress Series 76:249–260.

    Google Scholar 

  • Flint, R. W. and J. A. Younk. 1983. Estuarine benthos: long-term community structure variations, Corpus Christi Bay, Texas. Estuaries 6:126–141.

    Google Scholar 

  • Fuss, C. M., Jr. 1964. Observations on burrowing behavior of the pink shrimp, Penaeus duorarum Burkenroad. Bulletin of Marine Science, Gulf and Caribbean 14:62–73.

    Google Scholar 

  • Fuss, C. M. and L. H. Ogren. 1966. Factors affecting activity and burrowing habits of the pink shrimp, Penaeus duorarum Burkenroad. Biological Bulletin 130:170–191.

    Google Scholar 

  • Gleason, D. F. 1986. Utilization of salt marsh plants by postlarval brown shrimp: carbon assimilation rates and food preferences. Marine Ecology Progress Series 31:151–158.

    Google Scholar 

  • Gleason, D. F. and R. J. Zimmerman. 1984. Herbivory potential of postlarval brown shrimp associated with salt marshes. Journal of Experimental Marine Biology and Ecology 84:235–246.

    Article  Google Scholar 

  • Gosselink, J. G., C. L. Cordes and J. W. Parsons. 1979. An ecological characterization study of the Chenier Plain coastal ecosystem of Louisiana and Texas, Volumes. 1–3. U.S. Fish and Wildlife Service Report FWS-OBS-78/9, 10 & 11.

    Google Scholar 

  • Gunter, G. 1941. Death of fishes due to cold on the Texas coast, January, 1940. Ecology 22:203–208.

    Google Scholar 

  • -1942. Offatts Bayou, a locality with recurrent summer mortality of marine organisms. American Midland Naturalist 28:631–633.

    Google Scholar 

  • Gunter, G. and H. H. Hildebrand. 1951. Destruction of fishes and other organisms on the South Texas coast by the cold wave of January 28-February 3, 1951. Ecology 32:731–36.

    Google Scholar 

  • Heck, K. L., L. Coen, S. G. Morgan and R. K. Zimmer-Faust. 1994. Recruitment and habitat utilization by the blue crab Callinectes sapidus: the importance of juvenile nursery habitats to the fishery. Marine Fisheries Initiative (MARFIN) final report to NOAA National Marine Fisheries Service, St. Petersburg, Florida, USA.

    Google Scholar 

  • Heck, K. L. and L. D. Coen. 1995. Predation and the abundance of juvenile blue crabs: a comparison of selected East and Gulf Coast (USA) studies. Bulletin of Marine Science 57:877–883.

    Google Scholar 

  • Heck, K. L. and T. A. Thoman. 1981. Experiments on predator-prey interactions in vegetated aquatic habitats. Journal of Experimental Marine Biology and Ecology 53:125–134.

    Article  Google Scholar 

  • Heck, K. L. and K. A. Wilson. 1987. Predation rates on decapod crustaceans in latitudinally separated seagrass communities: a study of spatial and temporal variation using tethering techniques. Journal of Experimental Marine Biology and Ecology 107:87–100.

    Article  Google Scholar 

  • Herder, W. F. 1989. Nekton use of regularly flooded salt marsh cordgrass habitat in North Carolina, USA. Marine Ecology Progress Series 56:111–118.

    Google Scholar 

  • Hines, A. H. and G. M. Ruiz. 1995. Temporal variation in juvenile blue crab mortality: nearshore shallows and cannibalism in Chesapeake Bay. Bulletin of Marine Science 57:884–901.

    Google Scholar 

  • Johnson, M. C. and J. R. Fielding. 1956. Propagation of the white shrimp, Penaeus setiferus (Linn.) in captivity. Tulane Studies in Zoology 4:175–190.

    Google Scholar 

  • Klima, E. F., J. M. Nance, E. X. Martinez and T. Leary. 1990. Workshop on definition of shrimp recruitment overfishing. NOAA Technical Memorandum NMFS-SEFC-264.

    Google Scholar 

  • Kneib, R. T. 1984. Patterns of invertebrate distribution and abundance in the intertidal salt marsh: causes and questions. Estuaries 7:392–412.

    Google Scholar 

  • -1991. Flume weir for quantitative collection of nekton from vegetated intertidal habitats. Marine Ecology Progress Series 75:29–38.

    Article  Google Scholar 

  • -1995. Behaviour separates potential and realized effects of decapod crustaceans in salt marsh communities. Journal of Experimental Marine Biology and Ecology 193:239–256.

    Article  Google Scholar 

  • -1997. The role of tidal marshes in the ecology of estuarine nekton. Oceanography and Marine Biology: an Annual Review 35:163–220.

    Google Scholar 

  • Kneib, R. T. and M. K. Knowlton. 1995. Stage-structured interactions between seasonal and permanent residents of an estuarine nekton community. Oecologia 103:425–434.

    Article  Google Scholar 

  • Kneib, R. T. and S. L. Wagner. 1994. Nekton use of vegetated marsh habitats at different stages of tidal inundation. Marine Ecology Progress Series 106:227–238.

    Google Scholar 

  • Laughlin, R. A. 1982. Feeding habits of the blue crab, Callinectes sapidus Rathbun, in the Apalachicola estuary, Florida. Bulletin of Marine Science 32:807–822.

    Google Scholar 

  • Madden, C. J., J. W. Day and J. M. Randall. 1988. Freshwater and marine coupling in estuaries of the Mississippi River deltaic plain. Limnology and Oceanography 33:982–1004.

    CAS  Google Scholar 

  • Main, K. L. 1987. Predator avoidance in seagrass meadows: Prey behavior, microhabitat selection, cryptic coloration. Ecology 68:170–180.

    Google Scholar 

  • May, E. B. 1973. Extensive oxygen depletion in Mobile Bay, Alabama. Limnology and Oceanography 18:353–366.

    Article  CAS  Google Scholar 

  • McIvor, C. and L. P. Rozas. 1996. Direct nekton use of intertidal saltmarsh habitat and linkage with adjacent habitats: a review from the southeastern United States. Pages 311–334 in K. F. Nordstrom and C. T. Roman, editors. Estuarine shores: evolution, environments and human alterations. John Wiley & Sons, New York, New York, USA.

    Google Scholar 

  • McTigue, T. A. 1993. Trophic roles in juvenile Penaeus aztecus Ives and Penaeus setiferus (Linnaeus) in a Texas salt marsh. Dissertation. Texas A&M University, College Station, Texas, USA.

    Google Scholar 

  • McTigue, T. A. and R. J. Zimmerman. 1991. Carnivory versus herbivory in juvenile Penaeus setiferus (Linnaeus) and Penaeus aztecus (Ives). Journal of Experimental Marine Biology and Ecology 15:1–16.

    Google Scholar 

  • -1998. The use of infauna by juvenile Penaeus aztecus Ives and Penaeus setiferus (Linnaeus). Estuaries 21:160–175.

    Google Scholar 

  • Mense, D. J. and E. L. Wenner. 1989. Distribution and abundance of early life history stages of the blue crab, Callinectes sapidus, in tidal marsh creeks near Charleston, South Carolina. Estuaries 12:157–168.

    Google Scholar 

  • Minello, T. J. 1993. Chronographic tethering: a technique for measuring prey survival time and testing predation pressure in aquatic habitats. Marine Ecology Progress Series 101:99–104.

    Google Scholar 

  • -1999. Nekton densities in shallow estuarine habitats of Texas and Louisiana and the identification of Essential Fish Habitat. Pages 43–75 in L. Benaka, editor. Fish habitat: essential fish habitat and habitat rehabilitation. American Fisheries Society Symposium 22.

    Google Scholar 

  • Minello, T. J. and J. W. Webb, Jr. 1997. Use of natural and created Spartina alterniflora salt marshes by fishery species and other aquatic fauna in Galveston Bay, Texas, USA. Marine Ecology Progress Series 151:165–179.

    Google Scholar 

  • Minello, T. J., J. W. Webb, R. J. Zimmerman, R. B. Wooten, J. L. Martinez, T. J. Baumer and M. C. Pattillo. 1991. Habitat availability and utilization by benthos and nekton in Hall’s Lake and West Galveston Bay, NOAA Technical Memorandum, NMFS-SEFC-275.

    Google Scholar 

  • Minello, T. J. and R. B. Wooten, Jr. 1993. Effects of caging juvenile predators on benthic infaunal populations at experimental open bay disposal areas in Galveston Bay, Texas. Report to Galveston District of the U.S. Army Corps of Engineers. NationalMarine Fisheries Service, Galveston Laboratory, Galveston, Texas, USA.

    Google Scholar 

  • Minello, T. J. and R. J. Zimmerman. 1983. Fish predation on juvenile brown shrimp, Penaeus aztecus Ives: the effect of simulated Spartina structure on predation rates. Journal of Experimental Marine Biology and Ecology 72:211–231.

    Article  Google Scholar 

  • -1991. The role of estuarine habitats in regulating growth and survival of juvenile penaeid shrimp. Pages 1–16 in P. DeLoach, W. J. Dougherty and M. A. Davidson, editors. Frontiers in shrimp research. Elsevier Science Publishers, Amsterdam, The Netherlands.

    Google Scholar 

  • Minello, T. J., R. J. Zimmerman and E. X. Martinez. 1987. Fish predation on juvenile brown shrimp, Penaeus aztecus: effects of turbidity and substratum on predation rates. Fishery Bulletin, U.S. 85:59–70.

    Google Scholar 

  • -1989. Mortality of young brown shrimp Penaeus aztecus in estuarine nurseries. Transactions of the American Fisheries Society 118:693–708.

    Article  Google Scholar 

  • Minello, T. J., R. J. Zimmerman and R. Medina. 1994. The importance of edge for natant macrofauna in a created salt marsh. Wetlands 14:184–198.

    Article  Google Scholar 

  • Morris, J. T., B. Kjerfve and J. M. Dean. 1990. Dependence ofestuarine productivity on anomalies in mean sea level. Limnology and Oceanography 35:926–930.

    Article  Google Scholar 

  • Nance, J. M. 1993. Gulf of Mexico shrimp fishery recruitment overfishing definition: workshop 2. NOAA Technical Memorandum, NMFS-SEFSC-323.

    Google Scholar 

  • Nance, J. M., E. F. Klima and T. E. Czapla. 1989. Gulf of Mexico shrimp stock assessment workshop. NOAA Technical Memorandum, NMFS-SEFC-239.

    Google Scholar 

  • Neill, C. and L. A. Deegan. 1986. The effect of the Mississippi River delta lobe development on the habitat composition and diversity of Louisiana coastal wetlands. American Midland Naturalist 116:296–303.

    Google Scholar 

  • Nixon, S. W. 1980. Between coastal marshes and coastal waters-a review of twenty years of speculation and research on the role of salt marshes in estuarine productivity and water chemistry. Pages 437–524 in P. Hamilton and K. B. Macdonald, editors. Estuarine and wetland processes with emphasis on modeling. Plenum Press, New York, New York, USA.

    Google Scholar 

  • Orth, R. J., K. L. Heck and J. van Montfrans. 1984. Faunal communities in seagrass beds: a review of the influence of plant structure and prey characteristics on predator-prey relationships. Estuaries 7:339–350.

    Google Scholar 

  • Orth, R. J. and J. van Montfrans. 1982. Predator-prey interactions in a Zostera marina ecosystem in the lower Chesapeake Bay, Virginia. Pages 81–94 in R. J. Orth and J. van Montfrans, editors. Interactions of resident consumers in a temperate estuarine seagrass community: Vaucluse Shores, Virginia, USA. VIMS-SRAMSOE 267, Gloucester Point, Virginia, USA.

    Google Scholar 

  • Peters, D. S. and W. E. Schaaf. 1991. Empirical model of the trophic basis for fishery yield in coastal waters of the eastern USA. Transactions of the American Fisheries Society 120:459–473.

    Article  Google Scholar 

  • Peterson, G. W. and R. E. Turner. 1994. The value of salt marsh edge vs interior as a habitat for fish and decapod crustaceans in a Louisiana tidal marsh. Estuaries 17:235–262.

    Google Scholar 

  • Rabalais, N. N., F. R. Burditt, Jr., L. D. Coen, B. E. Cole, C. Eleuterius, K. L. Heck, Jr., T. A. McTigue, S. G. Morgan, H. M. Perry, F. M. Truesdale, R. K. Zimmer-Faust and R. J. Zimmerman. 1995. Settlement of Callinectes sapidus megalopae on artificial collectors in four Gulf of Mexico Estuaries. Bulletin of Marine Science 57:855–876.

    Google Scholar 

  • Reed, D. J. and D. R. Cahoon. 1992. The relationship between marsh surface topography, hydroperiod and growth of Spartina alterniflora in a deteriorating Louisiana salt marsh. Journal of Coastal Research 8:77–87.

    Google Scholar 

  • Rejmanek, M., C. E. Sasser and J. G. Gosselink. 1987. Modeling of vegetation dynamics in the Mississippi River deltaic plain. Vegetatio 69:133–140.

    Google Scholar 

  • Rosas, C., E. Lazarochavez and F. Buckleramirez. 1994. Feeding habits and food niche segregation of Callinectes sapidus, C. rathbunae and C. similis in a subtropical coastal lagoon of the Gulf of Mexico. Journal of Crustacean Biology 14:371–382.

    Google Scholar 

  • Rozas, L. P. 1993. Nekton use of salt marshes of the Southeast region of the United States. Pages 528–537 in O. Magoon, W. S. Wilson, H. Converse and L. T. Tobin, editors. Coastal Zone’ 93, Volume 2. Proceedings of the 8th symposium on coastal and ocean management, American Society Of Civil Engineers, New York, New York, USA.

    Google Scholar 

  • -1995. Hydroperiod and its influence on nekton use of the salt marsh: a pulsing ecosystem. Estuaries 18:579–590.

    Google Scholar 

  • Rozas, L. P. and D. J. Reed. 1993. Nekton use of marsh-surface habitats in Louisiana (USA) deltaic salt marshes undergoing submergence. Marine Ecology Progress Series 96:147–157.

    Google Scholar 

  • Rozas, L. P. and T. J. Minello. 1997. Estimating densities of small fishes and decapod crustaceans in shallow estuarine habitats: a review of sampling design with focus on gear selection. Estuaries 20:199–213.

    Google Scholar 

  • -1998. Nekton use of salt marsh, seagrass and nonvegetated habitats in a South Texas (USA) estuary. Bulletin of Marine Science 63:481–501.

    Google Scholar 

  • Ruiz, G. M., A. H. Hines and M. H. Posey. 1993. Shallow water as a refuge habitat for fish and crustaceans in nonvegetated estuaries — an example from Chesapeake Bay. Marine Ecology Progress Series 99:1–16.

    Google Scholar 

  • Ryer, C. H. 1987. Temporal patterns of feeding by blue crabs (Callinectes sapidus) in a tidal-marsh creek and adjacent seagrass meadow in the lower Chesapeake Bay. Estuaries 10:136–140.

    Google Scholar 

  • Sasser, C. E., M. D. Dozier, J. G. Gosselink and J. M. Hill. 1986. Spatial and temporal changes in Louisiana’s Barataria Basin marshes, 1945–80. Environmental Management 10:671–680.

    Article  Google Scholar 

  • Schindler, D. E., B. M. Johnson, N. A. Mackay, N. Bouwes and J. F. Kitchell. 1994. Crab:snail size-structured interactions and salt marsh predation gradients. Oecologia 97:49–61.

    Article  Google Scholar 

  • Sullivan, M. J. and C. A. Moncreiff. 1990. Edaphic algae are an important component of salt marsh food-webs: evidence from multiple stable isotope analyses. Marine Ecology Progress Series 62:149–159.

    Google Scholar 

  • Thomas, J. L. 1989. A comparative evaluation of Halodule wrightii Aschers, Spartina alterniflora Loisel and bare sand as nursery habitats for juvenile Callinectes sapidus (Rathbun). Dissertation. Texas A&M University, College Station, Texas, USA.

    Google Scholar 

  • Thomas, J. L., R. J. Zimmerman and T. J. Minello. 1990. Abundance patterns of juvenile blue crabs (Callinectes sapidus) in nursery habitats of two Texas bays. Bulletin of Marine Science 46:115–125.

    Google Scholar 

  • Turner, R. E. 1977. Intertidal vegetation and commercial yields of penaeid shrimp. Transactions of the American Fisheries Society 106:411–416.

    Article  Google Scholar 

  • -1997. Wetland loss in the northern Gulf of Mexico: multiple working hypotheses. Estuaries 20:1–13.

    Google Scholar 

  • Turner, R. E. and R. L. Allen. 1982. Bottom water oxygen concentration in the Mississippi River Delta Bight. Contributions in Marine Science 25:161–172.

    CAS  Google Scholar 

  • Turner, R. E. and Y. S. Rao. 1990. Relationships between wetland fragmentation and recent hydrologic changes in a deltaic coast. Estuaries 13:272–281.

    Google Scholar 

  • Turner, R. E., W. W. Schroeder and W. J. Wiseman. 1987. The role of stratification in the deoxygenation of Mobile Bay and adjacent shelf waters. Estuaries 10:13–19.

    CAS  Google Scholar 

  • Weinstein, M. P. 1979. Shallow marsh habitats as primary nurseries for fishes and shellfish, Cape Fear River, North Carolina. Fishery Bulletin, U.S. 77:339–358.

    Google Scholar 

  • Wells, J. T. 1987. Effects of sea-level rise on deltaic sedimentation in South-central Louisiana. Pages 157–166 in D. Nummendel, O. H. Pilkey and J. D. Howard, editors. Sea level change and coastal evolution. The Society of Economic Paleontologists and Mineralogists, Tulsa, Oklahoma, USA.

    Google Scholar 

  • Wenner, E. L. and H. R. Beatty. 1993. Utilization of shallow estuarine habitats in South Carolina, USA, by postlarval and juvenile stages of Penaeus spp. (Decapoda, Penaeidae). Journal of Crustacean Biology 13:280–295.

    Google Scholar 

  • West, D. L. and H. Williams. 1986. Predation by Callinectes sapidus (Rathbun) within Spartina alterniflora (Loisel) marshes. Journal of Experimental Marine Biology and Ecology 100:75–95.

    Article  Google Scholar 

  • Whaley, S. D. 1997. The effects of marsh edge and surface elevation on the distribution of salt marsh infauna and prey availability for nekton predators. Thesis, Texas A&M University, College Station, Texas, USA.

    Google Scholar 

  • Wheeler, R. S. 1969. Culture of penaeid shrimp in brackish-water ponds, 1966–67. Proceedings of the Southeast Association of Game and Fish Commissioners 22:387–391.

    Google Scholar 

  • Wilson, K. A., K. W. Able and K. L. Heck. 1990. Predation rates on juvenile blue crabs in estuarine nursery habitats: evidence for the importance of macroalgae (Ulva lactuca). Marine Ecology Progress Series 58:243–251.

    Google Scholar 

  • Wilson, K. A., K. L. Heck and K. W. Able. 1987. Juvenile blue crab, Callinectes sapidus, survival: an evaluation of eelgrass, Zostera marina, as refuge. Fishery Bulletin, U.S. 85:53–58.

    Google Scholar 

  • Zimmerman, R. J. and T. J. Minello 1984a. Densities of Penaeus aztecus, P. setiferus and other natant macrofauna in a Texas salt marsh. Estuaries 7:421–433.

    Google Scholar 

  • -1984b. Fishery habitat requirements: utilization of nursery habitats by juvenile penaeid shrimp in a Gulf of Mexico salt marsh. Pages 371–383 in B. J. Copeland, K. Hart, N. Davis and S. Friday, editors. Research for managing the nation’s estuaries. UNC-SG-84-08, UNC SeaGrant Publications, Raleigh, North Carolina, USA.

    Google Scholar 

  • Zimmerman, R. J., T. J. Minello, T. J. Baumer and M. C. Castiglione. 1989. Oyster reef as habitat for estuarine macrofauna. NOAA Technical Memorandum, NMFS-SEFC-249.

    Google Scholar 

  • Zimmerman, R. J., T. J. Minello, M. C. Castiglione and D. L. Smith 1990a. The use of Juncus and Spartina marshes by fisheries species in Lavaca Bay, Texas, with reference to effects of floods. NOAA Technical Memorandum, NMFS-SEFC-251.

    Google Scholar 

  • -1990b. Utilization of marsh and associated habitats along a salinity gradient in Galveston Bay. NOAA Technical Memorandum, NMFS-SEFC-250.

    Google Scholar 

  • Zimmerman, R. J., T. J. Minello, E. F. Klima and J. M. Nance. 1991. Effects of accelerated sea-level rise on coastal secondary production. Pages 110–124 in H. S. Bolton, editor. Coastal wetlands. American Society of Civil Engineers, New York, New York, USA.

    Google Scholar 

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Zimmerman, R.J., Minello, T.J., Rozas, L.P. (2002). Salt Marsh Linkages to Productivity of Penaeid Shrimps and Blue Crabs in the Northern Gulf of Mexico. In: Weinstein, M.P., Kreeger, D.A. (eds) Concepts and Controversies in Tidal Marsh Ecology. Springer, Dordrecht. https://doi.org/10.1007/0-306-47534-0_14

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  • DOI: https://doi.org/10.1007/0-306-47534-0_14

  • Publisher Name: Springer, Dordrecht

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