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Abstract

Seagrass meadows have extremely high primary and secondary productivity and support a great abundance and diversity of fish and invertebrates. A number of commercially and recreationally important species (including both fish and invertebrates) have been linked to seagrass at some stage of their life cycle, although few such species use seagrass throughout their life. Non-commercial species within seagrass may be an important food source for commercial species (forming trophic linkages). In addition, some species that do not inhabit seagrass may derive benefit from seagrass by way of exported seagrass detritus or resident/transient species that move out of seagrass (some of these topics are dealt with elsewhere in this volume: e.g. Heck and Orth, Chapter 22, Kenworthy et al., Chapter 25 and Bell et al., Chapter 26).

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References

  • Acosta CA and Butler MJ (1997) Role of mangrove habitat as a nursery for juvenile spiny lobster, Panulirus argus, in Belize. Mar Freshwater Res 48: 721–727

    Article  Google Scholar 

  • Anderson EE (1989) Economic benefits of habitat restoration: Seagrass and the Virginia hard-shell blue crab fishery. N Am J Fisheries Manag 9: 140–149

    Article  Google Scholar 

  • Arrivillaga A and Baltz DM (1999) Comparison of fishes and macroinvertebrates on seagrass and bare-sand sites on Guatemala's Atlantic coast. Bull Mar Sci 65: 301–319

    Google Scholar 

  • Beck MW, Heck KL, Able KW, Childers DL, Eggleston DB, Gillanders BM, Halpern B, Hays CG, Hoshino K, Minello TJ, Orth RJ, Sheridan PF and Weinstein MP (2001) The identification, conservation, and management of estuarine and marine nurseries for fish and invertebrates. Bioscience 51: 633–641

    Article  Google Scholar 

  • Bell JD and Pollard DA (1989) Ecology of fish assemblages and fisheries associated with seagrasses. In: Larkum AWD, McComb AJ and Shepherd SA (eds) Biology of Seagrasses: A Treatise on the Biology of Seagrasses with Special Reference to the Australasian Region, pp 565–609. Elsevier, Amsterdam

    Google Scholar 

  • Bell JD and Westoby M (1986a) Abundance of macrofauna in dense seagrass is due to habitat preference, not predation. Oecologia 68: 205–209

    Article  Google Scholar 

  • Bell JD and Westoby M (1986b) Importance of local changes in leaf height and density to fish and decapods associated with seagrasses. J Exp Mar Biol Ecol 104: 249–274

    Article  Google Scholar 

  • Bell JD and Westoby M (1986c) Variation in seagrass height and density over a wide spatial scale: Effects on common fish and decapods. J Exp Mar Biol Ecol 104: 275–295

    Article  Google Scholar 

  • Bell JD, Steffe AS and Westoby M (1985) Artificial seagrass: How useful is it for field experiments on fish and macroinvertebrates. J Exp Mar Biol Ecol 90: 171–177

    Article  Google Scholar 

  • Bell JD, Steffe AS and Westoby M (1988) Location of seagrass beds in estuaries: Effects on associated fish and decapods. J Exp Mar Biol Ecol 122: 127–146

    Article  Google Scholar 

  • Bell JD, Westoby M and Steffe AS (1987) Fish larvae settling in seagrass: Do they discriminate between beds of different leaf density? J Exp Mar Biol Ecol 111: 133–144

    Article  Google Scholar 

  • Bell JD and Worthington DG (1993) Links between estuaries and coastal rocky reefs in the lives of fishes from south-eastern Australia. In: Battershill CB, Schiel DR, Jones GP, Cresse RG and MacDiarmid AB (eds) Second International Temperate Reef Symposium, pp 85–91. Auckland, New Zealand. NIWA Marine, Wellington

    Google Scholar 

  • Bell SS and Hicks GRF (1991) Marine landscapes and faunal recruitment: A field test with seagrasses and copepods. Mar Ecol Prog Ser 73: 61–68

    Google Scholar 

  • Bell SS, Brooks RA, Robbins BD, Fonseca MS and Hall MO (2001) Faunal response to fragmentation in seagrass habitats: Implications for seagrass conservation. Biol Conserv 100: 115–123

    Article  Google Scholar 

  • Bell SS, Hall MO, Soffian S and Madley K (2002) Assessing the impact of boat propeller scars on fish and shrimp utilizing seagrass beds. Ecol Appl 12: 206–217

    Article  Google Scholar 

  • Bender DJ, Contreras TA and Fahrig L (1998) Habitat loss and population decline: A meta-analysis of the patch size effect. Ecology 79: 517–533

    Article  Google Scholar 

  • Beukers JS, Jones GP and Buckley RM (1995) Use of implant microtags for studies on populations of small reef fish. Mar Ecol Prog Ser 125: 61–66

    Google Scholar 

  • Blaber SJM, Cyrus DP, Albaret JJ, Ching CV, Day JW, Elliott M, Fonseca MS, Hoss DE, Orensanz J, Potter IC and Silvert W (2000) Effects of fishing on the structure and functioning of estuarine and nearshore ecosystems. ICES J Mar Sci 57: 590–602

    Article  Google Scholar 

  • Bologna PAX and Heck KL (1999) Differential predation and growth rates of bay scallops within a seagrass habitat. J Exp Mar Biol Ecol 239: 299–314

    Article  Google Scholar 

  • Bologna PAX and Heck KL (2000) Impacts of seagrass habitat architecture on bivalve settlement. Estuaries 23: 449–457

    Article  Google Scholar 

  • Brewer DT, Blaber SJM, Salini JP and Farmer MJ (1995) Feeding ecology of predatory fishes from Groote Eylandt in the Gulf of Carpentaria, Australia, with special reference to predation on penaeid prawns. Est Coast Shelf Sci 40: 577–600

    Article  Google Scholar 

  • Brown-Peterson NJ, Peterson MS, Rydene DA and Eames RW (1993) Fish assemblages in natural versus well-established recolonized seagrass meadows. Estuaries 16: 177–189

    Article  Google Scholar 

  • Butler A and Jernakoff P (1999) Seagrass in Australia. Strategic review and development of an R&D plan. CSIRO Publishing, Collingwood

    Google Scholar 

  • Cambridge ML and McComb AJ (1984) The loss of seagrass in Cockburn Sound, Western Australia. I. The time course and magnitude of seagrass decline in relation to industrial development. Aquat Bot 20: 229–243

    Article  Google Scholar 

  • Campana SE (1999) Chemistry and composition of fish otoliths: Pathways, mechanisms and applications. Mar Ecol Prog Ser 188: 263–297

    CAS  Google Scholar 

  • Cancemi G, De Falco G and Pergent G (2003) Effects of organic matter input from a fish farming facility on a Posidonia oceanica meadow. Est Coast Shelf Sci 56: 961–968

    Article  CAS  Google Scholar 

  • Connolly R, Jenkins G and Loneragan N (1999) Seagrass dynamics and fisheries sustainability. In: Butler A and Jernakoff P (eds) Seagrass in Australia. Strategic Review and Development of an R&D Plan, pp 25–64. CSIRO Publishing, Collingwood

    Google Scholar 

  • Connolly RM (1994a) A comparison of fish assemblages from seagrass and unvegetated areas of a southern Australian estuary. Aust J Mar Freshwater Res 45: 1033–1044

    Article  Google Scholar 

  • Connolly RM (1994b) Removal of seagrass canopy: Effects on small fish and their prey. J Exp Mar Biol Ecol 184: 99–110

    Article  Google Scholar 

  • Connolly RM (1997) Differences in composition of small, motile invertebrate assemblages from seagrass and unvegetated habitats in a southern Australian estuary. Hydrobiologia 346: 137–148

    Article  Google Scholar 

  • Connolly RM, Dalton A and Bass DA (1997) Fish use of an inundated saltmarsh flat in a temperate Australian estuary. Aust J Ecol 22: 222–226

    Article  Google Scholar 

  • Costa MJ, Santos CI and Cabral HN (2002) Comparative analysis of a temperate and a tropical seagrass bed fish assemblages in two estuarine systems: The Mira estuary (Portugal) and the Mussulo Lagoon (Angola). Cah Biol Mar 43: 73–81

    Google Scholar 

  • Davenport SR and Bax NJ (2002) A trophic study of a marine ecosystem off southeastern Australia using stable isotopes of carbon and nitrogen. Can J Fisheries Aquat Sci 59: 514–530

    Article  Google Scholar 

  • Dayton PK, Thrush SF, Agardy MT and Hofman RJ (1995) Environmental effects of marine fishing. Aquat Conserv: Mar Freshwater Ecosyst 5: 205–232

    Article  Google Scholar 

  • Delgado O, Ruiz J, Perez M, Romero J and Ballesteros E (1999) Effects of fish farming on seagrass (Posidonia oceanica) in a Mediterranean bay: Seagrass decline after organic loading cessation. Oceanologica Acta 22: 109–117

    Article  CAS  Google Scholar 

  • DiBacco C and Levin LA (2000) Development and application of elemental fingerprinting to track the dispersal of marine invertebrate larvae. Limnol Oceanogr 45: 871–880

    Article  CAS  Google Scholar 

  • Duarte CM (1999) Seagrass ecology at the turn of the millennium: Challenges for the new century. Aquat Bot 65: 7–20

    Article  Google Scholar 

  • Eckrich CE and Holmquist JG (2000) Trampling in a seagrass assemblage: Direct effects, response of associated fauna, and the role of substrate characteristics. Mar Ecol Prog Ser 201: 199–209

    Google Scholar 

  • Edgar GJ and Shaw C (1995a) The production and trophic ecology of shallow-water fish assemblages in southern Australia. I. Species richness, size-structure and production of fishes in Western Port, Victoria. J Exp Mar Biol Ecol 194: 53–81

    Article  Google Scholar 

  • Edgar GJ and Shaw C (1995b) The production and trophic ecology of shallow-water fish assemblages in southern Australia. II. Diets of fishes and trophic relationships between fishes and benthos at Western Port, Victoria. J Exp Mar Biol Ecol 194: 83–106

    Article  Google Scholar 

  • Edwards JW, Edyvane KS, Boxall VA, Hamann M and Soole KL (2001) Metal levels in seston and marine fish flesh near industrial and metropolitan centres in South Australia. Mar Pollut Bull 42: 389–396

    Article  PubMed  CAS  Google Scholar 

  • Eggleston DB, Etherington LL and Elis WE (1998a) Organism response to habitat patchiness: Species and habitat-dependent recruitment of decapod crustaceans. J Exp Mar Biol Ecol 223: 111–132

    Article  Google Scholar 

  • Eggleston DB, Grover JJ and Lipcius RN (1998b) Ontogenetic diet shifts in nassau grouper: Trophic linkages and predatory impact. Bull Mar Sci 63: 111–126

    Google Scholar 

  • Eggleston DB, Elis WE, Etherington LL, Dahlgren P and Posey MH (1999) Organism responses to habitat fragmentation and diversity: Habitat colonization by estuarine macrofauna. J Exp Mar Biol Ecol 236: 107–132

    Article  Google Scholar 

  • Fairweather PG (1999) Determining the ‘health' of estuaries: Priorities for ecological research. Aust J Ecol 24: 441–451

    Article  Google Scholar 

  • Ferrell DJ and Bell JD (1991) Differences among assemblages of fish associated with Zostera capricorni and bare sand over a large spatial scale. Mar Ecol Prog Ser 72: 15–24

    Google Scholar 

  • Ferrell DJ, McNeill SE, Worthington DG and Bell JD (1993) Temporal and spatial variation in the abundance of fish associated with the seagrass Posidonia australis in south-eastern Australia. Aust J Mar Freshwater Res 44: 881–899

    Article  Google Scholar 

  • Fonseca DM, Thayer GW, Chester AJ and Foltz C (1984) Impact of scallop harvesting on eelgrass (Zostera marina) meadows: Implications for management. N Am J Fisheries Manag 4: 286–293

    Article  Google Scholar 

  • Fonseca DM, Kenworthy WJ, Colby DR, Rittmaster KA and Thayer GW (1990) Comparisons of fauna among natural and transplanted eelgrass Zostera marina meadows: Criteria for mitigation. Mar Ecol Prog Ser 65: 251–264

    Google Scholar 

  • Fonseca MS, Meyer DL and Hall MO (1996) Development of planted seagrass beds in Tampa Bay, Florida, USA. II. Faunal components. Mar Ecol Prog Ser 132: 141–156

    Google Scholar 

  • Fry B (1981) Natural stable carbon isotope tag traces Texas shrimp migrations. Fishery Bull 79: 337–345

    Google Scholar 

  • Fry B (1983) Fish and shrimp migrations in the northern Gulf of Mexico analyzed using stable C, N and S isotope ratios. Fishery Bull 81: 789–801

    Google Scholar 

  • Fry B, Mumford PL and Robblee MB (1999) Stable isotope studies of pink shrimp (Farfantepenaeus duorarum Burkenroad) migrations on the southwestern Florida shelf. Bull Mar Sci 65: 419–430

    Google Scholar 

  • Gillanders BM (1997) Patterns of abundance and size structure in the blue groper Achoerodus viridis (Pisces: Labridae): Evidence of links between estuaries and coastal reefs. Environ Biol Fishes 49: 153–173

    Article  Google Scholar 

  • Gillanders BM (2002) Connectivity between juvenile and adult fish populations: Do adults remain near their recruitment estuaries? Mar Ecol Prog Ser 240: 215–223

    Google Scholar 

  • Gillanders BM and Kingsford MJ (1996) Elements in otoliths may elucidate the contribution of estuarine recruitment to sustaining coastal reef populations of a temperate reef fish. Mar Ecol Prog Ser 141: 13–20

    Google Scholar 

  • Gillanders BM, Able KW, Brown JA, Eggleston DB and Sheridan PF (2003) Evidence of connectivity between juvenile and adult habitats for mobile marine fauna: An important component of nurseries. Mar Ecol Prog Ser 247: 281–295

    Google Scholar 

  • Goldberg R, Phelan B, Pereira J, Hagan S, Clark P, Bejda A, Calabrese A, Studholme A and Able KW (2002) Variability in habitat use by young-of-the-year winter flounder, Pseudopleuronectes americanus, in three Northeastern U.S. estuaries. Estuaries 25: 215–226

    Google Scholar 

  • Gray CA, McElligott DJ and Chick RC (1996) Intra-and interestuary differences in assemblages of fishes associated with shallow seagrass and bare sand. Mar Freshwater Res 47: 723–735

    Article  Google Scholar 

  • Gray CA, Chick RC and McElligott DJ (1998) Diel changes in assemblages of fishes associated with shallow seagrass and bare sand. Est Coast Shelf Sci 46: 849–859

    Article  Google Scholar 

  • Greenway M (1995) Trophic relationships of macrofauna within a Jamaican seagrass meadow and the role of the echinoid Lytechinus variegatus (Lamarck). Bull Mar Sci 56: 719–736

    Google Scholar 

  • Griffiths SP (2001a) Diel variation in the seagrass ichthyofaunas of three intermittently open estuaries in south-eastern Australia: Implications for improving fish diversity assessments. Fisheries Manag Ecol 8: 123–140

    Article  Google Scholar 

  • Griffiths SP (2001b) Factors influencing fish composition in an Australian intermittently open estuary. Is stability salinitydependent? Est Coast Shelf Sci 52: 739–751

    Article  CAS  Google Scholar 

  • Guidetti P (2000) Differences among fish assemblages associated with nearshore Posidonia oceanica seagrass beds, rocky-algal reefs and unvegetated sand habitats in the Adriatic Sea. Est Coast Shelf Sci 50: 515–529

    Article  Google Scholar 

  • Guidetti P and Bussotti S (2002) Effects of seagrass canopy removal on fish in shallow Mediterranean seagrass (Cymodecea nodosa and Zostera noltii) meadows: A local-scale approach. Mar Biol 140: 445–453

    Article  Google Scholar 

  • Gunderson DR, Armstrong DA, Shi Y-B and McConnaughey RA (1990) Patterns of estuarine use by juvenile English sole (Parophyrys vetulus) and dungeness crab (Cancer magister). Estuaries 13: 59–71

    Article  Google Scholar 

  • Haddon M (2001) Modelling and quantitative methods in fisheries. Chapman and Hall, Boca Raton

    Google Scholar 

  • Hair CA, Bell JD and Kingsford MJ (1994) Effects of position in the water column, vertical movement and shade on settlement of fish to artificial habitats. Bull Mar Sci 55: 434–444

    Google Scholar 

  • Hamer PA and Jenkins GP (1996) Larval supply and shortterm recruitment of a temperate zone demersal fish, the King George whiting, Sillaginodes punctata Cuvier and Valenciennes, to an embayment in south-eastern Australia. J Exp Mar Biol Ecol 208: 197–214

    Article  Google Scholar 

  • Hammerstrom K, Sheridan P and McMahon G (1998) Potential for seagrass restoration in Galveston Bay, Texas. Tex J Sci 50: 35–50

    Google Scholar 

  • Hanekom N and Baird D (1984) Fish community structures in Zostera and non-Zostera regions of the Kromme estuary, St Francis Bay. S Afr J Zool 19: 295–301

    Google Scholar 

  • Hannan JC and Williams RJ (1998) Recruitment of juvenile marine fishes to seagrass habitat in a temperate Australian estuary. Estuaries 21: 29–51

    Article  Google Scholar 

  • Haywood MDE, Vance DJ and Loneragan NR (1995) Seagrass and algal beds as nursery habitats for tiger prawns (Penaeus semisulcatus and P. esculentus) inatropical Australian estuary. Mar Biol 122: 213–223

    Google Scholar 

  • Heck KL and Thoman TA (1981) Experiments on predator-prey interactions in vegetated aquatic habitats. J Exp Mar Biol Ecol 53: 125–134

    Article  Google Scholar 

  • Heck KL and Thoman TA (1984) The nursery role of seagrass meadows in the upper and lower reaches of the Chesapeake Bay. Estuaries 7: 70–92

    Article  Google Scholar 

  • Heck KL and Weinstein MP (1989) Feeding habits of juvenile reef fishes associated with Panamanian seagrass meadows. Bull Mar Sci 45: 629–636

    Google Scholar 

  • Heck KL and Wilson KA (1987) Predation rates on decapod crustaceans in latitudinally separated seagrass communities: A study of spatial and temporal variation using tethering techniques. J Exp Mar Biol Ecol 107: 87–100

    Article  Google Scholar 

  • Heck KL, Hays CG and Orth RJ (2003) A critical evaluation of the nursery role hypothesis for seagrass meadows. Mar Ecol Prog Ser 253: 123–136

    Google Scholar 

  • Heck KL, Nadeau DA and Thomas R (1997) The nursery role of seagrass beds. Gulf Mex Sci 15: 50–54

    Google Scholar 

  • Hindell JS, Jenkins GP and Keough MJ (2000a) Evaluating the impact of predation by fish on the assemblage structure of fishes associated with seagrass (Heterozostera tasmanica) (Martens ex Ascherson) den Hartog, and unvegetated sand habitats. J Exp Mar Biol Ecol 255: 153–174

    Article  Google Scholar 

  • Hindell JS, Jenkins GP and Keough MJ (2000b) Variability in abundances of fishes associated with seagrass habitats in relation to diets of predatory fishes. Mar Biol 136: 725–737

    Article  Google Scholar 

  • Hindell JS, Jenkins GP and Keough MJ (2001) Spatial and temporal variability in the effects of fish predation on macrofauna in relation to habitat complexity and cage effects. Mar Ecol Prog Ser 224: 231–250

    Google Scholar 

  • Hindell JS, Jenkins GP and Keough MJ (2002) Variability in the numbers of post-settlement King George whiting (Sillaginidae: Sillaginodes punctata, Cuvier) in relation to predation, habitat complexity and artificial cage structure. J Exp Mar Biol Ecol 268: 13–31

    Article  Google Scholar 

  • Hixon MA (1991) Predation as a process structuring coral reef fish communities. In: Sale PF (ed) The Ecology of Fishes on Coral Reefs, pp 475–508. Academic Press, San Diego

    Google Scholar 

  • Hobday DK, Officer RA and Parry GD (1999) Changes to demersal fish communities in Port Phillip Bay, Australia, over two decades, 1970–1991. Mar Freshwater Res 50: 397–407

    Google Scholar 

  • Hobson KA (1999) Tracing origins and migration of wildlife using stable isotopes: A review. Oecologia 120: 314–326

    Article  Google Scholar 

  • Hovel KA (2003) Habitat fragmentation in marine landscapes: Relative effects of habitat cover and configuration on juvenile crab survival in California and North Carolina seagrass beds. Biol Conserv 110: 401–412

    Article  Google Scholar 

  • Hovel KA and Lipcius RN (2001) Habitat fragmentation in a seagrass landscape: Patch size and complexity control blue crab survival. Ecology 82: 1814–1829

    Article  Google Scholar 

  • Hovel KA and Lipcius RN (2002) Effects of seagrass habitat fragmentation on juvenile blue crab survival and abundance. J Exp Mar Biol Ecol 271: 75–98

    Article  Google Scholar 

  • Hughes JE, Deegan LA, Wyda JC, Weaver MJ and Wright A (2002) The effects of eelgrass habitat loss on estuarine fish communities of southern New England. Estuaries 25: 235–249

    Google Scholar 

  • Irlandi EA (1994) Large-and small-scale effects of habitat structure on rates of predation: How percent coverage of seagrass affects rates of predation and siphon nipping on an infaunal bivalve. Oecologia 98: 176–183

    Article  Google Scholar 

  • Irlandi EA (1997) Seagrass patch size and survivorship of an infaunal bivalve. Oikos 78: 511–518

    Article  Google Scholar 

  • Irlandi EA and Peterson CH (1991) Modification of animal habitat by large plants: Mechanisms by which seagrasses influence clam growth. Oecologia 87: 307–318

    Article  Google Scholar 

  • Irlandi EA, Ambrose WG and Orlando BA (1995) Landscape ecology and the marine environment: How spatial configuration of seagrass habitat influences growth and survival of the bay scallop. Oikos 72: 307–313

    Article  Google Scholar 

  • Irlandi EA and Crawford MK (1997) Habitat linkages: The effect of intertidal saltmarshes and adjacent subtidal habitats on abundance, movement, and growth of an estuarine fish. Oecologia 110: 222–230

    Article  Google Scholar 

  • Irlandi EA, Orlando BA and Ambrose WG (1999) Influence of seagrass habitat patch size on growth and survival of juvenile bay scallops, Argopecten irradians concentricus (Say). J Exp Mar Biol Ecol 235: 21–43

    Article  Google Scholar 

  • Jackson EL, Rowden AA, Attrill MJ, Bossey SJ and Jones MB (2001) The importance of seagrass beds as a habitat for fishery species. Oceanogr Mar Biol Annu Rev 39: 269–303

    Google Scholar 

  • Jackson G and Jones GK (1999) Spatial and temporal variation in nearshore fish and macroinvertebrate assemblages from a temperate Australian estuary over a decade. Mar Ecol Prog Ser 182: 253–268

    Google Scholar 

  • Jenkins GP and Black KP (1994) Temporal variability in settlement of a coastal fish (Sillaginodes punctata) determined by low-frequency hydrodynamics. Limnol Oceanogr 39: 1744–1754

    Article  Google Scholar 

  • Jenkins GP and Sutherland CR (1997) The influence of habitat structure on nearshore fish assemblages in a southern Australian embayment: Colonisation and turnover rate of fishes associated with artificial macrophyte beds of varying physical structure. J Exp Mar Biol Ecol 218: 103–125

    Article  Google Scholar 

  • Jenkins GP and Wheatley MJ (1998) The influence of habitat structure on nearshore fish assemblages in a southern Australian embayment: Comparison of shallow seagrass, reefalgal and unvegetated sand habitats, with emphasis on their importance to recruitment. J Exp Mar Biol Ecol 221: 147–172

    Article  Google Scholar 

  • Jenkins GP and Hamer PA (2001) Spatial variation in the use of seagrass and unvegetated habitats by post-settlement King George whiting (Percoidei: Sillaginidae) in relation to meiofaunal distribution and macrophyte structure. Mar Ecol Prog Ser 224: 219–229

    Google Scholar 

  • Jenkins GP, Edgar GJH, May MA and Shaw C (1993) Ecological basis for parallel declines in seagrass habitat and catches of commercial fish in Western Port Bay, Victoria. In: Hancock DA (ed) Sustainable Fisheries Through Sustaining Fish Habitat, Australian Society for Fish Biology Workshop, Victor Harbour, SA, 12–13 August. Bureau of Resource Sciences Proceedings, Australian Government Publishing service, pp 124–136. Canberra

    Google Scholar 

  • Jenkins GP, Wheatley MJ and Poore AGB (1996) Spatial variation in recruitment, growth, and feeding of postsettlement King George whiting, Sillaginodes punctata, associated with seagrass beds of Port Phillip Bay, Australia. Can J Fisheries Aquat Sci 53: 350–359

    Article  Google Scholar 

  • Jenkins GP, Black KP, Wheatley MJ and Hatton DN (1997a) Temporal and spatial variability in recruitment of a temperate, seagrass-associated fish is largely determined by physical processes in the pre-and post-settlement phases. Mar Ecol Prog Ser 148: 23–35

    Google Scholar 

  • Jenkins GP, May HMA, Wheatley MJ and Holloway MG (1997b) Comparison of fish assemblages associated with seagrass and adjacent unvegetated habitats of Port Phillip Bay and Corner Inlet, Victoria, Australia, with emphasis on commercial species. Est Coast Shelf Sci 44: 569–588

    Article  Google Scholar 

  • Jenkins GP, Welsford DC, Keough MJ and Hamer PA (1998) Diurnal and tidal vertical migration of presettlement King George whiting Sillaginodes punctata in relation to feeding and vertical distribution of prey in a temperate bay. Mar Ecol Prog Ser 170: 239–248

    Google Scholar 

  • Jordan F, Bartolini M, Nelson C, Patterson PE and Soulen HL (1997) Risk of predation affects habitat selection by the pinfish Lagodon rhomboides (Linnaeus). J Exp Mar Biol Ecol 208: 45–56

    Article  Google Scholar 

  • Kendrick GA, Aylward MJ, Hegge BJ, Cambridge ML, Hillman K, Wyllie A and Lord DA (2002) Changes in seagrass coverage in Cockburn Sound, Western Australia between 1967 and 1999. Aquat Bot 73: 75–87

    Article  Google Scholar 

  • Kennedy BP, Folt CL, Blum JD and Chamberlain CP (1997) Natural isotope markers in salmon. Nature 387: 766–767

    Article  CAS  Google Scholar 

  • Koutsikopoulos C, Dorel D and Desaunay Y (1995) Movement of sole (Solea solea) inthe Bay of Biscay: Coastal environment and spawning migration. J Mar Biol Assoc UK 75: 109–126

    Google Scholar 

  • Laegdsgaard P and Johnson C (2001) Why do juvenile fish utilise mangrove habitats. J Exp Mar Biol Ecol 257: 229–253

    Article  PubMed  Google Scholar 

  • Laegdsgaard P and Johnson CR (1995) Mangrove habitats as nurseries: Unique assemblages of juvenile fish in subtropical mangroves in eastern Australia. Mar Ecol Prog Ser 126: 67–81

    Google Scholar 

  • Larkum AWD and West RJ (1990) Long-term changes of seagrass meadows in Botany Bay, Australia. Aquat Bot 37: 55–70

    Article  Google Scholar 

  • Lipcius RN and Van Engel WA (1990) Blue crab population dynamics in Chesapeake Bay: Variation in abundance (York River, 1972–1988) and stock recruit functions. Bull Mar Sci 46: 180–194

    Google Scholar 

  • Loneragan NR, Bunn SE and Kellaway DM (1997) Are mangroves and seagrasses sources of organic carbon for penaeid prawns in a tropical Australian estuary? A multiple stableisotope study. Mar Biol 130: 289–300

    Article  Google Scholar 

  • Loneragan NR, Kenyon RA, Staples DJ, Poiner IR and Conacher CA (1998) The influence of seagrass type on the distribution and abundance of postlarval and juvenile tiger prawns (Penaeus esculentus and P. semisulcatus) in the western Gulf of Carpentaria, Australia. J Exp Mar Biol Ecol 228: 175–195

    Article  Google Scholar 

  • Lubbers L, Boynton WR and Kemp WM (1990) Variations in structure of estuarine fish communities in relation to abundance of submersed vascular plants. Mar Ecol Prog Ser 65: 1–14

    Google Scholar 

  • MacArthur LD and Hyndes GA (2001) Differential use of seagrass assemblages by a suite of Odacid species. Est Coast Shelf Sci 52: 79–90

    Article  Google Scholar 

  • MacDonald CM (1992) Fluctuations in seagrass habitats and commercial fish catches in Westernport Bay and the Gippsland Lakes, Victoria. In: Hancock DA (ed) Recruitment Processes, pp 192–201. Australian Government Publishing Service, Canberra

    Google Scholar 

  • Matheson RE, Camp DK, Sogard SM and Bjorgo KA (1999) Changes in seagrass-associated fish and crustacean communities on Florida Bay mud banks: The effects of recent ecosystem changes? Estuaries 22: 534–551

    Article  Google Scholar 

  • McLaughlin PA, Treat SAF, Thorhaug A and Lemaitre R (1983) Arestored seagrass (Thalassia) bed and its animal community. Environ Conserv 10: 247–254

    Article  Google Scholar 

  • McNeill SE and Fairweather PG (1993) Single large or several small marine reserves? An experimental approach with seagrass fauna. J Biogeogr 20: 429–440

    Article  Google Scholar 

  • McNeill SE, Worthington DG, Ferrell DJ and Bell JD (1992) Consistently outstanding recruitment of five species of fish to a seagrass bed in Botany Bay, NSW. Aust J Ecol 15: 360–367

    Google Scholar 

  • Melville AJ and Connolly RM (2003) Spatial analysis of stable isotope data to determine primary sources of nutrition for fish. Oecologia 136: 499–507

    Article  PubMed  Google Scholar 

  • Meng L, Gray C, Taplin B and Kupcha E (2000) Using winter flounder growth rates to assess habitat quality in Rhode Island's coastal lagoons. Mar Ecol Prog Ser 201: 287–299

    Google Scholar 

  • Meyer DL, Fonseca MS, Murphey PL, McMichael RH, Byerly MM, Lacroix MW, Whitfield PE and Thayer GW (1999) Effects of live-bait shrimp trawling on seagrass beds and fish bycatch in Tampa Bay, Florida. Fishery Bull 97: 193–199

    Google Scholar 

  • Micheli F and Peterson CH (1999) Estuarine vegetated habitats as corridors for predator movements. Conserv Biol 13: 869–881

    Article  Google Scholar 

  • Middleton MJ, Bell JD, Burchmore JJ, Pollard DA and Pease BC (1984) Structural differences in the fish communities of Zostera capricorni and Posidonia australis seagrass meadows in Botany Bay, New South Wales. Aquat Bot 18: 89–109

    Article  Google Scholar 

  • Miller MJ and Able KW (2002) Movements and growth of tagged young-of-the-year Atlantic croaker (Micropogonias undulatus L.) in restored and reference marsh creeks in Delaware Bay, USA. J Exp Mar Biol Ecol 267: 15–33

    Article  Google Scholar 

  • Milton DA and Chenery SP (2001) Sources and uptake of trace metals in otoliths of juvenile barramundi (Lates calcarifer). J Exp Mar Biol Ecol 264: 47–65

    Article  CAS  Google Scholar 

  • Minello TJ (1993) Chronographic tethering: A technique for measuring prey survival time and testing predation pressure in aquatic habitats. Mar Ecol Prog Ser 101: 99–104

    Google Scholar 

  • Minello TJ, Able KW, Weinstein MP and Hays CG (2003) Salt marshes as nurseries for nekton: Testing hypotheses on density, growth, and survival through meta-analysis. Mar Ecol Prog Ser 246: 39–59

    Google Scholar 

  • Moncreiff CA and Sullivan MJ (2001) Trophic importance of epiphytic algae in subtropical seagrass beds: Evidence from multiple stable isotope analyses. Mar Ecol Prog Ser 215: 93–106

    CAS  Google Scholar 

  • Nagelkerken I, Dorenbosch M, Verberk WCEP, Cocheret de la Moriniere E and van der Velde G (2000a) Day-night shifts of fishes between shallow-water biotopes of a Caribbean bay, with emphasis on the nocturnal feeding of Haemulidae and Lutjanidae. Mar Ecol Prog Ser 194: 55–64

    Google Scholar 

  • Nagelkerken I, Dorenbosch M, Verberk WCEP, Cocheret de la Moriniere E and van der Velde G (2000b) Importance of shallow-water biotopes of a Caribbean bay for juvenile coral reef fishes: Patterns in biotope association, community structure and spatial distribution. Mar Ecol Prog Ser 202: 175–192

    Google Scholar 

  • Nagelkerken I, Kleijnen S, Klop T, van den Brand RACJ, Cocheret de la Moriniere E and van der Velde G (2001) Dependence of Caribbean reef fishes on mangroves and seagrass beds as nursery habitats: A comparison of fish faunas between bays with and without mangroves/seagrass beds. Mar Ecol Prog Ser 214: 225–235

    Google Scholar 

  • Nagelkerken I, Roberts CM, van der Velde G, Dorenbosch M, Van Riel MC, Cocheret de la Moriniere E and Nienhuis PH (2002) How important are mangroves and seagrass beds for coral-reef fish? The nursery hypothesis tested on an island scale. Mar Ecol Prog Ser 244: 299–305

    Google Scholar 

  • Nagelkerken I and van derVelde G (2002) Do non-estuarine mangroves harbour higher densities of juvenile fishes than adjacent shallow-water and coral reef habitats in Curacao (Netherlands Antilles)? Mar Ecol Prog Ser 245: 191–204

    Google Scholar 

  • Olney JE and Boehlert GW (1988) Nearshore ichthyoplankton associated with seagrass beds in the lower Chesapeake Bay. Mar Ecol Prog Ser 45: 33–43

    Google Scholar 

  • Orth RJ (1992) A perspective on plant-animal interactions in seagrasses: Physical and biological determinants influencing plant and animal abundance, In: John DM, Hawkins SJ and Price JH (eds) Plant–Animal Interactions in the Marine Benthos, pp 147–164. Clarendon Press, Oxford

    Google Scholar 

  • Orth RJ, Heck KL and van Montfrans J (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

    Article  Google Scholar 

  • Orth RJ and Moore KA (1983) Chesapeake Bay: An unprecedented decline in submerged aquatic vegetation. Science 222: 51–53

    Article  PubMed  CAS  Google Scholar 

  • Orth RJ and van Montfrans J (1987) Utilisation of a seagrass meadow and tidal marsh creek by blue crabs Callinectes sapidus. I. Seasonal and annual variations in abundance with emphasis on post-settlement juveniles. Mar Ecol Prog Ser 41: 283–294

    Google Scholar 

  • Orth RJ and van Montfrans J (1990) Utilization of marsh and seagrass habitats by early stages of Callinectes sapidus: A latitudinal perspective. Bull Mar Sci 46: 126–144

    Google Scholar 

  • Orth RJ and van Montfrans J (2002) Habitat quality and prey size as determinants of survival in post-larval and early juvenile instars of the blue crab Callinectes sapidus. Mar Ecol Prog Ser 231: 205–213

    Google Scholar 

  • Parrish JD (1989) Fish communities of interacting shallow-water habitats in tropical oceanic regions. Mar Ecol Prog Ser 58: 143–160

    Google Scholar 

  • Peterman RM (1990) Statistical power analysis can improve fisheries research and management. Can J Fisheries Aquat Sci 47: 2–15

    Google Scholar 

  • Peterson BJ and Fry B (1987) Stable isotopes in ecosystem studies. Annu Rev Ecol Systematics 18: 293–320

    Article  Google Scholar 

  • Peterson CH, Summerson HC and Fegley SR (1987) Ecological consequences of mechanical harvesting of clams. Fishery Bull 85: 281–298

    Google Scholar 

  • Peterson BJ, Thompson KR, Cowan JH and Heck KL (2001) Comparison of predation pressure in temperate and subtropical seagrass habitats based on chronographic tethering. Mar Ecol Prog Ser 224: 77–85

    Google Scholar 

  • Petrik R, Levin PS, Stunz GW and Malone J (1999) Recruitment of Atlantic croaker, Micropogonias undulatus: Do postsettlement processes disrupt or reinforce initial patterns of settlement? Fishery Bull 97: 954–961

    Google Scholar 

  • Phelan BA, Goldberg R, Bejda AJ, Pereira J, Hagan S, Clark P, Studholme AL, Calabrese A and Able KW (2000) Estuarine and habitat-related differences in growth rates of young of-the-year winter flounder (Pseudopleuronectes americanus) and tautog (Tautoga onitis) in three northeastern US estuaries. J Exp Mar Biol Ecol 247: 1–28

    Article  PubMed  Google Scholar 

  • Pinto L and Punchihewa NN (1996) Utilisation of mangroves and seagrasses by fishes in the Negombo estuary, Sri Lanka. Mar Biol 126: 333–345

    Article  Google Scholar 

  • Pulich WM and White WA (1991) Decline of submerged vegetation in the Galveston Bay system: Chronology and relationships to physical processes. J Coastal Res 7: 1125–1138

    Google Scholar 

  • Rapport DJ, Costanza R, and McMichael AJ (1998) Assessing ecosystem health. Trends Ecol Evol 13: 397–402

    Article  Google Scholar 

  • Rasmussen E (1977) The wasting disease of eelgrass (Zostera marina) and its effect on environmental factors and fauna. In: McRoy CP and Helfferich C (eds) Seagrass Ecosystems: A Scientific Perspective, pp 1–51. Marcel Dekker, New York.

    Google Scholar 

  • Robbins BD and Bell SS (1994) Seagrass landscapes: A terrestrial approach to the marine subtidal environment. Trends Ecol Evol 9: 301–304

    Article  Google Scholar 

  • Robblee MB and Zieman JC (1984) Diel variation in the fish fauna of a tropical seagrass feeding ground. Bull Mar Sci 34: 335–345

    Google Scholar 

  • Robblee MB, Barber TR, Carlson PR, Durako MJ, Fourqurean JW, Muehlstein LK, Porter D, Yarbro LA, Zieman RT and Zieman JC (1991) Mass mortality of the tropical seagrass Thalassia testudinum in Florida Bay (USA). Mar Ecol Prog Ser 71: 297–299

    Google Scholar 

  • Robertson AI (1980) The structure and organization of an eelgrass fish fauna. Oecologia 47: 76–82

    Article  Google Scholar 

  • Robertson AI and Duke NC (1987) Mangroves as nursery sites: Comparisons of the abundance and species composition of fish and crustraceans in mangroves and other nearshore habitats in tropical Australia. Mar Biol 96: 193–205

    Article  Google Scholar 

  • Rooker JR and Holt SA (1997) Utilization of subtropical seagrass meadows by newly settled red drum Sciaenops ocellatus: Patterns of distribution and growth. Mar Ecol Prog Ser 158: 139–149

    Google Scholar 

  • Rooker JR, Holt GJ and Holt SA (1998a) Vulnerability of newly settled red drum (Sciaenops ocellatus) to predatory fish: Is early-life survival enhanced by seagrass meadows? Mar Biol 131: 145–151

    Article  Google Scholar 

  • Rooker JR, Holt SA, Soto MA and Holt GJ (1998b) Postsettlement patterns of habitat use by sciaenid fishes in subtropical seagrass meadows. Estuaries 21: 318–327

    Article  Google Scholar 

  • Rozas LP and Minello TJ (1998) Nekton use of salt marsh, seagrass, and nonvegetated habitats in a south Texas (USA) estuary. Bull Mar Sci 63: 481–501

    Google Scholar 

  • Ruckelshaus MH and Hays CG (1998) Conservation and management of species in the sea. In: Fiedler PL and Kareiva PM (eds) Conservation Biology for the Coming Decade, pp 112–156. Chapman and Hall, New York

    Google Scholar 

  • Ruello NV (1975) Geographical distribution, growth and breeding migration of the eastern Australian king prawn Penaeus plebejus Hess. Aust J Mar Freshwater Res 26: 343–354

    Article  Google Scholar 

  • Ruello NV (1977) Migration and stock studies on the Australian school prawn Metapenaeus macleayi. Mar Biol 41: 185–190

    Article  Google Scholar 

  • Ruiz JM, Perez M and Romero J (2001) Effects of fish farm loadings on seagrass (Posidonia oceanica) distribution, growth and photosynthesis. Mar Pollut Bull 42: 749–760

    Article  PubMed  CAS  Google Scholar 

  • Ryer CH, van Montfrans J and Moody KE (1997) Cannibalism, refugia and the molting blue crab. Mar Ecol Prog Ser 147: 77–85

    Google Scholar 

  • Salita JT, Ekau W and Saint-Paul U (2003) Field evidence on the influence of seagrass landscapes on fish abundance in Bolinao, northern Philippines. Mar Ecol Prog Ser 247: 183–195

    Google Scholar 

  • Sanchez-Jerez P and Ramos-Espla AA (1996) Detection of environmental impacts by bottom trawling on Posidonia oceanica (L.) Delile meadows: Sensitivity of fish and macrobenthic communities. J Aquat Ecosyst Health 5: 239–253

    Article  Google Scholar 

  • Sanchez-Jerez P and Ramos-Espla A (2000) Changes in fish assemblages associated with the deployment of an antitrawling reef in seagrass meadows. Trans Am Fisheries Soc 129: 1150–1159

    Article  Google Scholar 

  • Scott LC, Boland JW, Edyvane KS and Jones GK (2000) Development of a seagrass-fish habitat model-I: A seagrass residency index for economically important species. Environmetrics 11: 541–552

    Article  Google Scholar 

  • Seddon S, Connolly RM and Edyvane KS (2000) Large-scale seagrass dieback in northern Spencer Gulf, South Australia. Aquat Bot 66: 297–310

    Article  Google Scholar 

  • Sheaves M (1995) Large lutjanid and serranid fishes in tropical estuaries: Are they adults or juveniles. Mar Ecol Prog Ser 129: 31–40

    Google Scholar 

  • Sheridan PF (1992) Comparative habitat utilization by estuarine macrofauna within the mangrove ecosystem of Rookery Bay, Florida. Bull Mar Sci 50: 21–39

    Google Scholar 

  • Sheridan P (1997) Benthos of adjacent mangrove, seagrass and non-vegetated habitats in Rookery Bay, Florida, USA. Est Coast Shelf Sci 44: 455–469

    Article  Google Scholar 

  • Sheridan P and Hays C (2003) Are mangroves nursery habitat for transient fishes and decapods? Wetlands 23: 449–458

    Article  Google Scholar 

  • Sheridan P, McMahon G, Conley G, Williams A and Thayer G (1997) Nekton use of macrophyte patches following mortality of turtlegrass, Thalassia testudinum, in shallow waters of Florida Bay (Florida, USA). Bull Mar Sci 61: 801–820

    Google Scholar 

  • Sheridan P, Henderson C and McMahon G (2003) Fauna of natural seagrass and transplanted Halodule wrightii (shoalgrass) beds in Galveston Bay, Texas. Restor Ecol 11: 139–154

    Article  Google Scholar 

  • Sogard SM (1989) Colonization of artificial seagrass by fishes and decapod crustaceans: Importance of proximity to natural eelgrass. J Exp MarBiol Ecol 133: 15–37

    Article  Google Scholar 

  • Sogard SM (1992) Variability in growth rates of juvenile fishes in different estuarine habitats. Mar Ecol Prog Ser 85: 35–53

    Google Scholar 

  • Sogard SM and Able KW (1991) A comparison of eelgrass, sea lettuce macroalgae, and marsh creeks as habitats for epibenthic fishes and decapods. Est Coast Shelf Sci 33: 501–519

    Article  Google Scholar 

  • Sogard SM and Able KW (1994) Diel variation in immigration of fishes and decapod crustaceans to artificial seagrass habitat. Estuaries 17: 622–630

    Article  Google Scholar 

  • Sogard SM, Powell GVN and Holmquist JG (1987) Epibenthic fish communities on Florida Bay banks: Relations with physical parameters and seagrass cover. Mar Ecol Prog Ser 40: 25–39

    Google Scholar 

  • Sogard SM, Powell GVN and Holmquist JG (1989a) Spatial distribution and trends in abundance of fishes residing in seagrass meadows on Florida Bay mudbanks. Bull Mar Sci 44: 179–199

    Google Scholar 

  • Sogard SM, Powell GVN and Holmquist JG (1989b) Utilization by fishes of shallow, seagrass-covered banks in Florida Bay: 1. Species composition and spatial heterogeneity. Environ Biol Fishes 24: 53–65

    Article  Google Scholar 

  • Sogard SM, Powell GVN and Holmquist JG (1989c) Utilization by fishes of shallow, seagrass-covered banks in Florida Bay: 2. Diel and tidal patterns. Environ Biol Fishes 24: 81–92

    Article  Google Scholar 

  • Steffe AS, Westoby M and Bell JD (1989) Habitat selection and diet in two species of pipefish from seagrass: Sex differences. Mar Ecol Prog Ser 55: 23–30

    Google Scholar 

  • Stunz GW and Minello TJ (2001) Habitat-related predation on juvenile wild-caught and hatchery-reared red drum Sciaenops ocellatus (Linnaeus). J Exp Mar Biol Ecol 260: 13–25

    Article  PubMed  Google Scholar 

  • StunzGW, Minello TJ and Levin PS (2002) Growth of newly settled red drum Sciaenops ocellatus in different estuarine habitat types. Mar Ecol Prog Ser 238: 227–236

    Google Scholar 

  • Swearer SE, Caselle JE, Lea DW and Warner RR (1999) Larval retention and recruitment in an island population of a coralreef fish. Nature 402: 799–802

    Article  CAS  Google Scholar 

  • Tanner JE (2003) Patch shape and orientation influences on seagrass epifauna are mediated by dispersal abilities. Oikos 100: 517–524

    Article  Google Scholar 

  • Thayer GW and Phillips RC (1977) Importance of eelgrass beds in Puget Sound. Mar Fisheries Rev 39: 18–22

    Google Scholar 

  • Thayer GW, Murphey PL and LaCroix MW (1994) Responses of plant communities in western Florida Bay to the die-off of seagrasses. Bull Mar Sci 54: 718–726

    Google Scholar 

  • Thomas BE and Connolly RM (2001) Fish use of subtropical saltmarshes in Queensland, Australia: Relationships with vegetation, water depth, and distance onto the marsh. Mar Ecol Prog Ser 209: 275–288

    Google Scholar 

  • Thorrold SR, Latkoczy C, Swart PK and Jones CM (2001) Natal homing in a marine fish metapopulation. Science 291: 297–299

    Article  PubMed  CAS  Google Scholar 

  • Thresher RE, Nichols PD, Gunn JS, Bruce BD and Furlani DM (1992) Seagrass detritus as the basis of a coastal planktonic food chain. Limnol Oceanogr 37: 1754–1758

    Article  Google Scholar 

  • Tupper M and Boutilier RG (1995) Effects of habitat on settlement, growth, and postsettlement survival of Atlantic cod (Gadus morhua). Can J Fisheries Aquat Sci 52: 1834–1841

    Article  Google Scholar 

  • Turner MG (1989) Landscape ecology: The effect of pattern on process. Annu Rev Ecol Syst 20: 171–197

    Article  Google Scholar 

  • Turner SJ, Hewitt JE, Wilkinson MR, Morrisey DJ, Thrush SF, Cummings VJ and Funnell G (1999) Seagrass patches and landscapes: The influence of wind-wave dynamics and hierarchical arrangements of spatial structure on macrofaunal seagrass communities. Estuaries 22: 1016–1032

    Article  Google Scholar 

  • Underwood AJ (1996) Detection, interpretation, prediction and management of environmental disturbances: Some roles for experimental marine ecology. J Exp Mar Biol Ecol 200: 1–27

    Article  Google Scholar 

  • Vanderklift MA and Jacoby CA (2003) Patterns in fish assemblages 25 years after seagrass loss. Mar Ecol Prog Ser 247: 225–235

    Google Scholar 

  • Villard MA, Trzcinski MK and Merriam G (1999) Fragmentation effects on forest birds: Relative influence of woodland cover and configuration on landscape occupancy. Conserv Biol 13: 774–783

    Article  Google Scholar 

  • Wiens JA (1989) Spatial scaling in ecology. Funct Ecol 3: 385–397

    Article  Google Scholar 

  • Weinstein MP and Heck KL (1979) Ichthyofauna of seagrass meadows along the Caribbean coast of Panama and in the Gulf of Mexico: Composition, structure and community ecology. Mar Biol 50: 97–107

    Article  Google Scholar 

  • Worthington DG, Westoby M and Bell JD (1991) Fish larvae settling in seagrass: Effects of leaf density and an epiphytic alga. Aust J Ecol 16: 289–293

    Article  Google Scholar 

  • Worthington DG, Ferrell DJ, McNeill SE and Bell JD (1992) Effects of the shoot density of seagrass on fish and decapods: Are correlation evident over larger spatial scales? Mar Biol 112: 139–146

    Article  Google Scholar 

  • Wyda JC, Deegan LA, Hughes JE and Weaver MJ (2002) The response of fishes to submerged aquatic vegetation complexity in two ecoregions of the Mid-Atlantic bight: Buzzards Bay and Chesapeake Bay. Estuaries 25: 86–100

    Article  Google Scholar 

  • Zacherl DC, Manriquez PH, Paradis G, Day RW, Castilla JC, Warner RR, Lea DW and Gaines SD (2003) Trace elemental fingerprinting of gastropod statoliths to study larval dispersal trajectories. Mar Ecol Prog Ser 248: 297–303

    CAS  Google Scholar 

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Gillanders, B.M. (2007). Seagrasses, Fish, and Fisheries. In: SEAGRASSES: BIOLOGY, ECOLOGYAND CONSERVATION. Springer, Dordrecht. https://doi.org/10.1007/978-1-4020-2983-7_21

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