Skip to main content

Advertisement

Log in

The role of seagrass meadows, mangrove forests, salt marshes and reed beds as nursery areas and food sources for fishes in estuaries

  • Reviews
  • Published:
Reviews in Fish Biology and Fisheries Aims and scope Submit manuscript

Abstract

Each year millions of larval and 0+ juvenile fishes are recruited into estuarine fish populations around the world. For several decades the roles of littoral aquatic and emergent macrophyte habitats as nursery areas for many of these species have been studied and debated at length. This review attempts to collate the published literature and provide a synopsis of the varying, and sometimes conflicting, views on this topic. A large number of studies have shown that a range of species and an abundance of juvenile fishes are associated with littoral macrophytes in estuaries, some of which are found almost exclusively within particular plant habitats. Other studies have shown the movement of certain juvenile fishes from one type of littoral plant habitat to another as they grow and develop new feeding strategies and dietary requirements. Overall, it would appear that seagrass beds and mangrove forests are particularly favoured by fishes as nursery areas in both estuaries and the nearshore marine environment, and that the loss of these habitats leads to a decline in juvenile fish diversity and abundance. Salt marshes and reed beds generally have a lower diversity of fishes than seagrass and mangrove habitats, possibly due to the more temperate location of salt marshes and the dense structure of some reed beds. Stable isotope studies in particular are providing increasing evidence that carbon assimilated by juvenile fishes in mangrove, marsh and reed habitats is not primarily derived from these macrophytes but comprises a mixture of these sources and a diverse range of macro- and microalgae, particularly epiphytic, epipsammic, epipelic and epilithic diatoms and algae found in these areas. The closest trophic link between the macrophyte food chain and associated fishes occurs in seagrass habitats where a significant portion of the overall macrophyte leaf biomass often consists of epiphytic algae and diatoms. Structurally, mangrove forests, salt marshes and reed beds provide more substantial and complex habitats for juvenile fish refuge, but some of these habitats are constrained with regard to nursery provision by being fully exposed at low tide. Under such circumstances the small fish are sometimes forced into creeks and channels where larger piscivorous fishes are often present. Overall, in terms of a broad ranking of the four habitats as potential fish nursery areas, seagrass meadows are ranked first, followed by mangrove forests, salt marshes and then reed beds. This ranking does not imply that the lower ranked habitats are unimportant, since these plants perform a myriad of ecosystem services that are not related to the provision of fish nursery areas, e.g. bank stabilization. It is also emphasized that the protection of specific plant species should not be encouraged because it is important to have an ecosystem approach to conservation so that the diversity of habitats and their connectivity for fishes is maintained.

This is a preview of subscription content, log in via an institution to check access.

Access this article

Price excludes VAT (USA)
Tax calculation will be finalised during checkout.

Instant access to the full article PDF.

Fig. 1
Fig. 2
Fig. 3

Similar content being viewed by others

References

  • Able KW (1999) Measures of juvenile fish habitat quality: examples from a National Estuarine Research Reservc. Am Fish Soc Symp 22:134–147

    Google Scholar 

  • Able KW (2005) A re-examination of fish estuarine dependence: evidence for connectivity between estuarine and ocean habitats. Estuar Coast Shelf Sci 64:5–17

    Article  Google Scholar 

  • Able KW, Hagan SM (2000) Effects of common reed (Phragmites australis) invasion on marsh surface macrofauna: responses of fishes and decapod crustaceans. Estuaries 23:633–646

    Article  Google Scholar 

  • Able KW, Hagan SM (2003) Impact of common reed, Phragmites australis, on essential fish habitat: influence on reproduction, embryological development, and larval abundance of mummichog (Fundulus heteroclitus). Estuaries 26:40–50

    Article  Google Scholar 

  • Able KW, Nemerson DM, Bush R, Light P (2001) Spatial variation in Delaware Bay (USA) marsh creek fish assemblages. Estuaries 24:441–452

    Article  Google Scholar 

  • Able KW, Hagan SM, Brown SA (2003) Mechanisms of marsh habitat alteration due to Phragmites: response of young-of-the-year mummichog (Fundulus heteroclitus) to treatment for Phragmites removal. Estuaries 26:484–494

    Article  Google Scholar 

  • Aburto-Oropeza O, Ezcurra E, Danemann G, Valdez V, Murray J, Sala E (2008) Mangroves in the Gulf of California increase fishery yields. Proc Nat Acad Sci USA 105:10456–10459

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  • Adams SM (1976a) Feeding ecology of eelgrass fish communities. Trans Am Fish Soc 105:514–519

    Article  Google Scholar 

  • Adams SM (1976b) The ecology of eelgrass, Zostera marina (L.), fish communities. I. Structural analysis. J Exp Mar Biol Ecol 22:269–291

    Article  Google Scholar 

  • Adams AJ, Locascio JV, Robbins BD (2004) Microhabitat use by a post-settlement stage estuarine fish: evidence from relative abundance and predation among habitats. J Exp Mar Biol Ecol 299:17–33

    Article  Google Scholar 

  • Ayvazian SG, Deegan LA, Finn JT (1992) Comparison of habitat use by estuarine fish assemblages in the Acadian and Virginian zoogeographic provinces. Estuaries 15:368–383

    Article  Google Scholar 

  • Baltz DM, Rakocinski C, Fleeger JW (1993) Microhabitat use by marsh-edge fishes in a Louisiana estuary. Env Biol Fish 36:109–126

    Article  Google Scholar 

  • Baltz DM, Fleeger JW, Rakocinski C, McCall JN (1998) Food, density, and microhabitat: factors affecting growth and recruitment potential of juvenile saltmarsh fishes. Env Biol Fish 53:89–103

    Article  Google Scholar 

  • Barbier EB, Hacker SD, Kennedy C, Koch EW, Stier AC, Silliman BR (2011) The value of estuarine and coastal ecosystem services. Ecol Monogr 81:169–193

    Article  Google Scholar 

  • Barletta M, Barletta-Bergan A, Saint-Paul U, Hubold G (2003) Seasonal changes in density, biomass, and diversity of estuarine fishes in tidal mangrove creeks of the lower Caetá Estuary (northern Brazilian coast, east Amazon). Mar Ecol Prog Ser 256:217–228

    Article  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, Weinstein MP (2001) The identification, conservation, and management of estuarine and marine nurseries for fish and invertebrates. Bioscience 51:633–641

    Article  Google Scholar 

  • Becker A, Laurenson LJB (2007) Seasonal and diel comparisons of the diets of four dominant fish species within the main channel and flood-zone of a small intermittently open estuary in south-eastern Australia. Mar Freshw Res 58:1086–1095

    Article  Google Scholar 

  • Becker A, Cowley PD, Whitfield AK (2010) Use of remote underwater video to record littoral habitat use by fish within a temporarily closed estuary South African estuary. J Exp Mar Biol Ecol 391:161–168

    Article  Google Scholar 

  • Beckley LE (1983) The ichthyofauna associated with Zostera capensis Setchell in the Swartkops estuary, South Africa. S Afr J Zool 18:15–24

    Article  Google Scholar 

  • Bell JD, Pollard DA (1989) Ecology of fish assemblages and fisheries associated with seagrasses. In: Larkum AWD et al (eds) Biology of seagrasses. Elsevier, Amsterdam, pp 565–597

    Google Scholar 

  • Bell JD, Westoby M (1986) 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, Pollard DA, Burchmore JJ, Pease BC, Middleton MJ (1984) Structure of a fish community in a temperate tidal mangrove creek in Botany Bay, New South Wales. Aust J Mar Freshw Res 35:33–46

    Article  Google Scholar 

  • Bell JD, Steffe AS, 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 

  • Beumer JP (1978) Feeding ecology of four fishes from a mangrove creek in north Queensland, Australia. J Fish Biol 12:475–490

    Article  Google Scholar 

  • Blaber SJM (1974) Field studies of the diet of Rhabdosargus holubi (Pisces: Teleostei: Sparidae). J Zool Lond 173:407–417

    Article  Google Scholar 

  • Blaber SJM (1980) Fishes of the Trinity Inlet system of North Queensland with notes on the ecology of fish faunas of tropical Indo-Pacific estuaries. Aust J Mar Freshw Res 31:137–146

    Article  Google Scholar 

  • Blaber SJM (1982) The ecology of Sphyraena barracuda (Osteichthyes: Perciformes) in the Kosi system with notes on other Natal estuaries. S Afr J Zool 17:171–176

    Article  Google Scholar 

  • Blaber SJM (2007) Mangroves and fishes: issues of diversity, dependence, and dogma. Bull Mar Sci 80:457–472

    Google Scholar 

  • Bloomfield AL, Gillanders BM (2005) Fish and invertebrate assemblages in seagrass, mangrove, saltmarsh, and nonvegetated habitats. Estuaries 28:63–77

    Article  Google Scholar 

  • Boesch DF, Turner RE (1984) Dependence of fishery species on salt marshes: the role of food and refuge. Estuaries 7:460–468

    Article  Google Scholar 

  • Boström C, Jackson EL, Simonstad CA (2006) Seagrass landscapes and their effects on associated fauna: a review. Estuar Coast Shelf Sci 68:383–403

    Article  Google Scholar 

  • Bouillon S, Koedam N, Raman AV, Dehairs F (2002) Primary producers sustaining macro-invertebrate communities in intertidal mangrove forests. Oecologia 130:441–448

    Article  Google Scholar 

  • Bozeman EL, Dean JM (1980) The abundance of estuarine larval and juvenile fish in a South Carolina intertidal creek. Estuaries 3:89–97

    Article  Google Scholar 

  • Branch GM, Grindley JR (1979) Ecology of southern African estuaries Part XI. Mngazana: a mangrove estuary in the Transkei. S Afr J Zool 14:149–170

    Article  Google Scholar 

  • Carr WES, Adams CA (1973) Food habits of juvenile marine fishes occupying seagrass beds in the estuarine zone near Crystal River, Florida. Trans Am Fish Soc 102:511–540

    Article  Google Scholar 

  • Cattrijsse A, Hampel H (2006) European intertidal marshes: a review of their habitat functioning and value for aquatic organisms. Mar Ecol Prog Ser 324:293–307

    Article  Google Scholar 

  • Cattrijsse A, Makwaia ES, Dankwa HR, Hamerlynck O, Hemminga MA (1994) Nekton communities of an estuarine tidal creek of a European estuarine brackish marsh. Mar Ecol Prog Ser 109:195–208

    Article  Google Scholar 

  • Cattrijsse A, Dankwa HR, Mees J (1997) Nursery function of an estuarine tidal marsh for the brown shrimp Crangon crangon. J Sea Res 38:109–121

    Article  Google Scholar 

  • Chamberlain RH, Barnhart RA (1993) Early use by fish of a mitigation salt marsh, Humboldt Bay, California. Estuaries 16:769–783

    Article  Google Scholar 

  • Chittaro PM, Usseglio P, Sale PF (2005) Variation in fish density, assemblage composition and relative rates of predation among mangrove, seagrass and coral reef habitats. Environ Biol Fish 72:175–187

    Article  Google Scholar 

  • Chong VC (2007) Mangroves-fisheries linkages—the Malaysian perspective. Bull Mar Sci 80:755–772

    Google Scholar 

  • Chong VC, Sasekumar A, Leh MUC, D’Cruz R (1990) The fish and prawn communities of a Malaysian coastal mangrove system, with comparisons to adjacent mud flats and inshore waters. Estuar Coast Shelf Sci 31:703–722

    Article  Google Scholar 

  • Clynick B, Chapman MG (2002) Assemblages of small fish in patchy mangrove forests in Sydney Harbour. Mar Freshw Res 53:669–677

    Article  Google Scholar 

  • Coetzee DJ, Pool RC (1991) Diet of the larger fish species in the Breede River estuary, with emphasis on the prey species Palaemon capensis. Bontebok 7:27–35

    Google Scholar 

  • Coles RG, Lee WJ, Watson RA, Derbyshire KJ (1993) Distribution of seagrasses, and their fish and penaeid prawn communities, in Cairns harbour, a tropical estuary, Northern Queensland, Australia. Mar Freshw Res 44:193–201

    Google Scholar 

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

    Article  Google Scholar 

  • Connolly RM, Dalton A, 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, Costa JL, de Almeida PR, Assis CA (1994) Do eel grass beds and salt marsh borders act as preferential nurseries and spawning grounds for fish? An example of the Mira estuary in Portugal. Ecol Eng 3:187–195

    Article  Google Scholar 

  • Costa MJ, Catarino F, Bettencourt A (2001) The role of salt marshes in the Mira estuary (Portugal). Wetl Ecol Manag 9:121–134

    Article  Google Scholar 

  • Craig JK, Crowder LB (2000) Factors influencing habitat selection in fishes with a review of marsh ecosystems. In: Weinstein MP, Kreeger DA (eds) Concepts and controversies in tidal marsh ecology. Springer, Netherlands, pp 241–266

    Google Scholar 

  • Crona BI, Rönnbäck P (2007) Community structure and temporal variability of juvenile fish assemblages in natural and replanted mangroves, Sonneratia alba Sm., of Gazi Bay, Kenya. Estuar Coast Shelf Sci 74:44–52

    Article  Google Scholar 

  • Dahlgren CP, Kellison GT, Adams AJ, Gillanders BM, Kendall MS, Layman CA, Ley JA, Nagelkerken I, Serafy JE (2006) Marine nurseries and effective juvenile habitats: concepts and applications. Mar Ecol Prog Ser 312:291–295

    Article  Google Scholar 

  • Daniel PA, Robertson AI (1990) Epibenthos of mangrove waterways and open embayments: community structure and the relationship between exported mangrove detritus and epifaunal standing stocks. Estuar Coast Shelf Sci 31:599–619

    Article  Google Scholar 

  • Deegan LA (2002) Lessons learned: the effects of nutrient enrichment on the support of nekton by seagrass and salt marsh ecosystems. Estuaries 25:727–742

    Article  CAS  Google Scholar 

  • Deegan LA, Hughes JE, Rountree RA (2000) Salt marsh ecosystem support of marine transient species. In: Weinstein MP, Kreeger DA (eds) Concepts and controversies in tidal marsh ecology. Springer, Netherlands, pp 333–365

    Google Scholar 

  • Deegan LA, Wright A, Ayvazian SG, Finn JT, Golden H, Merson RR, Harrison J (2002) Nitrogen loading from upland areas alters seagrass support of higher trophic levels. Aquat Conserv Mar Freshw Ecosys 12:195–212

    Article  Google Scholar 

  • Desmond JS, Zedler JB, Williams GD (2000) Fish use of tidal creek habitats in two southern California salt marshes. Ecol Eng 14:233–252

    Article  Google Scholar 

  • Dionne M, Short FT, Burdick DM (1999) Fish utilization of restored, created, and reference salt-marsh habitat in the Gulf of Maine. Am Fish Soc Symp 22:384–404

    Google Scholar 

  • Dorenbosch M, Grol MGG, Nagelkerken I, van der Velde G (2006) Different surrounding landscapes may result in different fish assemblages in East African seagrass beds. Hydrobiol 563:45–60

    Article  Google Scholar 

  • Edgar GJ (1990) The influence of plant structure on the species richness, biomass and secondary production of macrofaunal assemblages associated with West Australian seagrass beds. J Exp Mar Biol Ecol 137:215–240

    Article  Google Scholar 

  • Edgar GJ, Shaw C (1995) The production and trophic ecology of shallow-water fish assemblages in southern Australia III. General relationships between sediments, seagrasses, invertebrates and fishes. J Exp Mar Biol Ecol 194:107–131

    Article  Google Scholar 

  • Edworthy C, Strydom N (2016) Habitat partitioning of juvenile fishes in a temperate estuarine nursery South Africa. Sci Mar 80:151–161

    Article  Google Scholar 

  • Emmerson WD (1986) The ecology of Palaemon pacificus (Stimpson) associated with Zostera capensis Setchell. Trans R Soc S Afr 46:79–97

    Article  Google Scholar 

  • Enríquez S, Duarte CM, Sand-Jensen K (1993) Patterns in decomposition rates among photosynthetic organisms: the importance of detritus C:N: P content. Oecologia 94:457–471

    Article  Google Scholar 

  • Erftemeijer PLA, Allen GR (1993) Fish fauna of seagrass beds in south Sulawesi, Indonesia. Res West Aust Mus 16:259–277

    Google Scholar 

  • Faunce CH, Serafy JE (2006) Mangroves as fish habitat: 50 years of field studies. Mar Ecol Prog Ser 318:1–18

    Article  Google Scholar 

  • Fell PE, Weissbach SP, Jones DA, Fallon MA, Zeppieri JA, Faison EK, Lennon KA, Newberry KJ, Reddington LK (1998) Does invasion of oligohaline tidal marshes by reed grass, Phragmites australis (Cav.) Trin. Ex Steud., affect the availability of prey resources for the mummichog, Fundulus heteroclitus L.? J Exp Mar Biol Ecol 222:59–77

    Article  Google Scholar 

  • Fell PE, Warren RS, Light JK, Rawson RL, Fairley SM (2003) Comparison of fish and macroinvertebrate use of Typha angustifolia, Phragmites australis, and treated Phragmites marshes along the lower Connecticut River. Estuaries 26:534–551

    Article  Google Scholar 

  • Ferrell DJ, 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

    Article  Google Scholar 

  • Ferrell DJ, McNeill SE, Worthington DG, 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 Freshw Res 44:881–899

    Article  Google Scholar 

  • Flores-Verdugo F, González-Farías F, Ramíez-Flores O (1990) Mangrove ecology, aquatic primary productivity, and fish community dynamics in the Teacapán-Agua Brava Lagoon-estuarine system (Mexican Pacific). Estuaries 13:219–230

    Article  Google Scholar 

  • Fodrie FJ, Levin LA, Lucas AJ (2009) Use of population fitness to evaluate the nursery function of juvenile habitats. Mar Ecol Prog Ser 385:39–49

    Article  Google Scholar 

  • Fodrie FJ, Heck KL, Powers S, Graham WM, Robinson KL (2010) Climate-related, decadal-scale assemblage changes of seagrass-associated fishes in the northern Gulf of Mexico. Glob Change Biol 16:48–59

    Article  Google Scholar 

  • França S, Costa MJ, Cabral HN (2009) Assessing habitat specific fish assemblages in estuaries along the Portuguese coast. Estuar Coast Shelf Sci 83:1–12

    Article  Google Scholar 

  • Franco A, Franzoi P, Malavasi S, Riccato F, Torricelli P, Mainardi D (2006) Use of shallow water habitats by fish assemblages in a Mediterranean coastal lagoon. Estuar Coast Shelf Sci 66:67–83

    Article  Google Scholar 

  • Frankovich TA, Zieman JC (2005) A temporal investigation of grazer dynamics, nutrients, seagrass leaf productivity, and epiphyte standing stock. Estuaries 28:41–52

    Article  Google Scholar 

  • Fry B, Ewel KC (2003) Using stable isotopes in mangrove fisheries research—a review and outlook. Isot Environ Health Stud 39:191–196

    Article  CAS  Google Scholar 

  • Gell FR, Whittington MW (2002) Diversity of fishes in seagrass beds in the Quirimba Archipelago, northern Mozambique. Mar Freshw Res 53:115–121

    Article  Google Scholar 

  • Giarrizzo T, Krumme U (2007) Spatial differences and seasonal cyclicity in the intertidal fish fauna from four mangrove creeks in a salinity zone of the Curuçá Estuary, north Brazil. Bull Mar Sci 80:739–754

    Google Scholar 

  • Gillanders BM (1997) Patterns of abundance and size structure in the blue groper, Achoerodus viridus (Pisces, Labridae): evidence of links between estuaries and coastal reefs. Env Biol Fish 49:153–173

    Article  Google Scholar 

  • Gillanders BM (2006) Seagrasses, fish, and fisheries. In: Larkum A, Orth RJ, Carlos D (eds) Seagrasses: biology, ecology and conservation. Springer, Netherlands, pp 503–505

    Google Scholar 

  • Gillanders BM, Able KW, Brown JA, Eggleston DB, 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

    Article  Google Scholar 

  • Gratwicke B, Speight MR (2005) The relationship between fish species richness, abundance and habitat complexity in a range of shallow tropical marine habitats. J Fish Biol 66:650–667

    Article  Google Scholar 

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

    Article  Google Scholar 

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

    Article  Google Scholar 

  • Grol MGG, Dorenbosch M, Kokkelmans EMG, Nagelkerken I (2008) Mangroves and seagrass beds do not enhance growth of early juveniles of a coral reef fish. Mar Ecol Prog Ser 336:137–146

    Article  Google Scholar 

  • Guest MA, Connolly RM, Loneragan NR (2003) Seine nets and beam trawls compared by day and night for sampling fish and crustaceans in shallow seagrass habitat. Fish Res 64:185–196

    Article  Google Scholar 

  • Gullström M, Bodin M, Nilsson PG, Öhman MC (2008) Seagrass structural complexity and landscape configuration as determinants of tropical fish assemblage composition. Mar Ecol Prog Ser 363:241–255

    Article  Google Scholar 

  • Halliday IA, Young WR (1996) Density, biomass and species composition of fish in a subtropical Rhizophora stylosa mangrove forest. Mar Freshw Res 47:609–615

    Article  Google Scholar 

  • Halpin PM (2000) Habitats use by an intertidal salt-marsh fish: trade-offs between predation and growth. Mar Ecol Prog Ser 198:203–214

    Article  Google Scholar 

  • Hampel H, Cattrijsse Elliott M (2005) Feeding habits of young predatory fishes in marsh creeks situated along the salinity gradient of the Schelde estuary, Belgium and The Netherlands. Helgol Mar Res 59:151–162

    Article  Google Scholar 

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

    Article  Google Scholar 

  • Harrison PG, Mann KH (2003) Detritus formation from eelgrass (Zostera marina L.): the relative effects of fragmentation, leaching, and decay. Limnol Oceanogr 20:924–934

    Article  Google Scholar 

  • Heck KL, Orth RJ (1980) Seagrass habitats: the roles of habitat complexity, competition and predation in structuring associated fish and motile invertebrate assemblages. In: Kennedy VS (ed) Estuarine perspectives. Academic Press, New York, pp 449–464

    Chapter  Google Scholar 

  • Heck KL, 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, Able KW, Fahay MP, Roman CT (1989) Fishes and decapod crustaceans of Cape Cod eelgrass meadows: species composition, seasonal abundance patterns and comparison with unvegetated substrates. Estuaries 12:59–65

    Article  Google Scholar 

  • Heck KL, Able KW, Roman CT, Fahay MP (1995) Composition, abundance, biomass and production of macrofauna in a New England estuary: comparisons among eelgrass meadows and other nursery habitats. Estuaries 18:379–389

    Article  Google Scholar 

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

    Article  Google Scholar 

  • Heck KL, Carruthers TJB, Duarte CM, Hughes AR, Kendrick G, Orth RJ, Williams SW (2008) Trophic transfers from seagrass meadows subsidize diverse marine and terrestrial consumers. Ecosystems 11:1198–1210

    Article  Google Scholar 

  • Herke WH, Knudsen EE, Knudsen PA, Rogers BD (1992) Effects of semi-impoundment of Louisiana marsh on fish and crustacean nursery use and export. N Am J Fish Man 12:151–160

    Article  Google Scholar 

  • Hettler WF (1989) Nekton use of regularly-flooded saltmarsh cordgrass habitat in North Carolina, USA. Mar Ecol Prog Ser 56:111–118

    Article  Google Scholar 

  • Hindell JS, Jenkins GP (2004) Spatial and temporal variability in the assemblage structure of fishes associated with mangroves (Avicennia marina) and intertidal mudflats in temperate Australian embayments. Mar Biol 144:385–395

    Article  Google Scholar 

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

    Article  Google Scholar 

  • Holt SA, Kitting CL, Arnold CR (1983) Distribution of young red drums among different sea-grass meadows. Trans Am Fish Fish Soc 112:267–271

    Article  Google Scholar 

  • Honda K, Nakamura Y, Nakaoka M, Uy WH, Fortes MD (2013) Habitat use by fishes in coral reefs, seagrass beds and mangrove habitats in the Philippines. PLoS ONE 8:e65735. doi:10.1371/journal.pone.0065735

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  • Horinouchi M, Kume G, Yamaguchi A, Toda K, Kurata K (2008) Food habits of small fishes in a common reed Phragmites australis belt in Lake Shinji, Shimane, Japan. Ichthyol Res 55:207–217

    Article  Google Scholar 

  • Hosack GR, Dumauld BR, Ruesink JL, Armstrong DA (2006) Habitat associations of estuarine species: comparisons of intertidal mudflat, seagrass (Zostera marina), and oyster (Crassostrea gigas) habitats. Estuar Coast 29:1150–1160

    Article  Google Scholar 

  • Hoss DE, Thayer GW (1993) The importance of habitat to the early life history of estuarine dependent fishes. Am Fish Soc Symp 14:147–158

    Google Scholar 

  • Hughes EH, Sherr EB (1983) Subtidal food webs in a Georgia estuary: δ13C analysis. J Exp Mar Biol Ecol 57:227–242

    Article  Google Scholar 

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

    Article  Google Scholar 

  • Hughes AR, Williams SL, Duarte CM, Heck KL, Waycott M (2008) Associations of concern: declining seagrasses and threatened dependent species. Front Ecol Environ 7:242–246

    Article  Google Scholar 

  • Huijbers CM, Mollee EM, Nagelkerken I (2008) Post-larval French grunts (Haemulon flavolineatum) distinguish between seagrass, mangrove and coral reef water: implications for recognition of potential nursery habitats. J Exp Mar Biol Ecol 357:134–139

    Article  Google Scholar 

  • Humphries P, Potter IC, Loneragan NR (1992) The fish community in the shallows of a temperate Australian estuary: relationships with the aquatic macrophyte Ruppia megacarpa and environmental variables. Estuar Coast Shelf Sci 34:325346

    Article  Google Scholar 

  • Hunter KL, Fox DA, Brown LM, Able KW (2006) Responses of resident marsh fishes to stages of Phragmites australis invasion in three mid Atlantic estuaries. Estuar Coast 29:487–498

    Article  Google Scholar 

  • Huxham M, Kimani E, Augley J (2004) Mangrove fish: a comparison of community structure between forested and cleared habitats. Estuar Coast Shelf Sci 60:637–647

    Article  Google Scholar 

  • Ikejima K, Tongnunui P, Medej T, Taniuchi T (2003) Juvenile and small fishes in a mangrove estuary in Trang Province, Thailand: seasonal and habitat differences. Estuar Coast Shelf Sci 56:447–457

    Article  Google Scholar 

  • Irlandi EA, 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 

  • Islam S, Haque M (2004) The mangrove-based coastal and nearshore fisheries of Bangladesh: ecology, exploitation and management. Rev Fish Biol Fish 14:153–180

    Article  Google Scholar 

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

    Google Scholar 

  • Jelbart JE, Ross PM, Connolly RM (2007) Fish assemblages in seagrass beds are influenced by the proximity of mangrove forests. Mar Biol 150:993–1002

    Article  Google Scholar 

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

    Article  Google Scholar 

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

    Article  Google Scholar 

  • Jin B, Fu C, Zong J, Li B, Chen J, Wu J (2007) Fish utilization of a salt marsh intertidal creek in the Yangtze River estuary, China. Estuar Coast Shelf Sci 73:852–884

    Article  Google Scholar 

  • Karosienė J, Kasperovičienė J (2012) Peculiarities of epiphyton algal communities formation on different macrophyte species. Bot Lith 18:154–163

    Google Scholar 

  • Kikuchi T (1974) Japanese contributions on consumer ecology in eelgrass (Zostera marina) beds, with special reference to trophic relationships and resources in inshore fisheries. Aquaculture 4:145–160

    Article  Google Scholar 

  • Kimirei IA, Nagelkerken I, Mgaya YD, Huijbers CM (2013) The mangrove nursery paradigm revisited: otolith stable isotopes support nursery-to-reef movements by Indo-Pacific fishes. PLoS ONE 8:e66320. doi:10.1371/journal.pone.0066320

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  • Kneib RN (1984) Patterns in the utilization of the intertidal salt marsh by larvae and juveniles of Fundulus heteroclitus (Linnaeus) and Fundulus luciae (Baird). J Exp Mar Biol Ecol 83:41–51

    Article  Google Scholar 

  • Kneib RN (1997) The role of tidal marshes in the ecology of estuarine nekton (Eds, Ansell AD, Gibson RN, Barnes M). Oceanogr Mar Biol Ann Rev 35:163–220

    Google Scholar 

  • Kneib RN (2000) Salt marsh ecoscapes and production transfers by estuarine nekton in the southeastern United States. In: Weinstein MP, Kreeger DA (eds) Concepts and controversies in tidal marsh ecology. Springer, Netherlands, pp 267–291

    Google Scholar 

  • Koenig CC, Coleman FC, Eklund A-M, Schull J, Ueland J (2007) Mangroves as essential habitat for goliath grouper (Epinephelus itajara). Bull Mar Sci 80:567–585

    Google Scholar 

  • Kulczycki GR, Virnstein RW, Nelson WG (1981) The relationship between fish abundance and algal biomass in a seagrass-drift algae community. Estuar Coast Shelf Sci 12:341–347

    Article  Google Scholar 

  • Kwak SN, Klumpp DW (2004) Temporal variation in species composition and abundance of fish and decapods of a tropical seagrass bed in Cockle Bay, north Queensland, Australia. Aquat Bot 78:119–134

    Article  Google Scholar 

  • Kwak TJ, Zedler JB (1997) Food web analysis of southern California coastal wetlands using multiple stable isotopes. Oecologia 110:262–277

    Article  Google Scholar 

  • Laegdsgaard P, 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

    Article  Google Scholar 

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

    Article  CAS  PubMed  Google Scholar 

  • Laffaille P, Brosse S, Feunteun E, Baisez A, Lefeuvre J-C (1998) Role of fish communities in particulate organic matter fluxes between salt marshes and coastal marine waters in the Mont Saint-Michel Bay. Hydrobiol 373–374:121–133

    Article  Google Scholar 

  • Laffaille P, Feunteun E, Lefeuvre J-C (2000) Composition of fish communities in a European macrotidal salt marsh (the Mont Saint-Michel Bay, France). Estuar Coast Shelf Sci 51:429–438

    Article  Google Scholar 

  • Laffaille P, Lefeuvre J-C, Schricke M-T, Feunteun E (2001) Feeding ecology of 0-group sea bass, Dicentrachus labrax, in salt marshes of Mont Saint Michel Bay (France). Estuaries 24:116–125

    Article  Google Scholar 

  • Laffaille P, Pétillon J, Parlier E, Valery L, Ysnel F, Radureau A, Feunteun E, Lefeuvre J-C (2005) Does the invasive plant Elymus athericus modify fish diet in tidal salt marshes? Estuar Coast Shelf Sci 65:739–746

    Article  Google Scholar 

  • Layman CA, Silliman BR (2002) Preliminary survey and diet analysis of juvenile fishes of an estuarine creek on Andros Island, Bahamas. Bull Mar Sci 70:199–210

    Google Scholar 

  • Layman CA, Arrington DA, Langerhans RB, Silliman BR (2004) Degree of fragmentation affects fish assemblage structure in Andros Island (Bahamas) estuaries. Caribb J Sci 40:232–244

    Google Scholar 

  • Lazzari MA, Sherman S, Kanwit JK (2003) Nursery use of shallow habitats by epibenthic fishes in Maine nearshore waters. Estuar Coast Shelf Sci 56:73–84

    Article  Google Scholar 

  • Le Marie M, van der Zaag P, Menting G, Baquete E, Schotanus D (2006) The use of remote sensing for monitoring environmental indicators: the case of the Incomati estuary, Mozambique. Phys Chem Earth 31:857–863

    Article  Google Scholar 

  • Le Quesne WJF (2000) Nekton utilisation of intertidal estuarine marshes in the Knysna Estuary. Trans R Soc S Afr 55:205–214

    Article  Google Scholar 

  • Leber KM (1983) Feeding ecology of decapod crustaceans and the influence of vegetation on foraging success in a subtropical seagrass meadow. PhD thesis, Florida State University, Tallahassee

  • Lee SY (1998) Ecological role of grapsid crabs in mangrove ecosystems: a review. Mar Freshw Res 49:335–343

    Article  Google Scholar 

  • Lefeuvre J-C, Laffaille P, Feunteun E (1999) Do fish communities function as biotic vectors of organic matter between salt marshes and marine coastal waters. Aquat Ecol 33:293–299

    Article  Google Scholar 

  • Leslie TD (2015) Assessing estuarine nursery habitats for Cape stumpnose (Rhabdosargus holubi), (Pisces: Sparidae) in a warm-temperate estuary in the Eastern Cape, South Africa. MSc thesis, Rhodes University, Grahamstown

  • Ley JA, McIvor CC, Montague CL (1999) Fishes in mangrove prop-root habitats of northeastern Florida Bay: distinct assemblages across an estuarine gradient. Estuar Coast Shelf Sci 48:701–723

    Article  Google Scholar 

  • Livingston RJ (1982) Trophic organization of fishes in a coastal seagrass system. Mar Ecol Prog Ser 7:1–12

    Article  Google Scholar 

  • Livingston RJ (1984a) The relationship of physical factors and biological response in coastal seagrass meadows. Estuaries 7:377–390

    Article  Google Scholar 

  • Livingston RJ (1984b) Trophic response of fishes to habitat variability in coastal seagrass systems. Ecology 65:1258–1275

    Article  Google Scholar 

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

    Article  Google Scholar 

  • Lugendo BR, Pronker A, Cornelissen I, de Groene A, Nagelkerken I, Dorenbosch M, van der Velde G, Mgaya YD (2005) Habitat utilisation by juveniles of commercially important fish species in a marine embayment in Zanzibar, Tanzania. Aquat Living Resour 18:149–158

    Article  Google Scholar 

  • Lugendo BR, Nagelkerken I, van der Velde G, Mgaya YD (2006) The importance of mangroves, mud and sand flats, and seagrass beds as feeding areas for juvenile fishes in Chwaka Bay, Zanzibar: gut content and stable isotope analyses. J Fish Biol 69:1639–1661

    Article  CAS  Google Scholar 

  • Lukey JR, Booth AJ, Froneman PW (2006) Fish population size and movement patterns in a small intermittently open South African estuary. Estuar Coast Shelf Sci 67:10–20

    Article  Google Scholar 

  • Luo J, Serafy JE, Sponaugle S, Teare PB, Kieckbusch D (2009) Movement of gray snapper Lutjanus griseus among subtropical seagrass, mangrove, and coral reef habitats. Mar Ecol Prog Ser 380:255–269

    Article  Google Scholar 

  • Manson FJ, Loneragan NR, Skilleter GA, Phinn SR (2005) An evaluation of the evidence for linkages between mangroves and fisheries: a synthesis of the literature and identification of research directions. Oceanogr Mar Biol 43:485–515

    Google Scholar 

  • Mathieson S, Cattrijsse A, Costa MJ, Drake P, Elliott M, Gardner J, Marchand J (2000) Fish assemblages of European tidal marshes: a comparison based on species, families and functional guilds. Mar Ecol Prog Ser 204:225–242

    Article  Google Scholar 

  • Mazumder D, Saintilan N, Williams RJ (2006) Trophic relationships between itinerant fish and crab larvae in a temperate Australian saltmarsh. Mar Freshw Res 57:193–199

    Article  Google Scholar 

  • Mbande S, Froneman W, Whitfield A (2004) The primary carbon sources utilised by fishes in the Mngazi and Mngazana estuaries, South Africa: a preliminary assessment. Afr J Aquat Sci 29:195–204

    Article  Google Scholar 

  • Mbande S, Whitfield AK, Cowley PD (2005) The ichthyofaunal composition of the Mngazi and Mngazana estuaries: a comparative study. Smith Bull 4:1–20

    Google Scholar 

  • McIvor CC, Odum WE (1988) Food, predation risk, and microhabitat selection in a marsh fish assemblage. Ecology 69:1341–1351

    Article  Google Scholar 

  • McIvor CC, Smith TJ (1995) Differences in the crab fauna of mangrove areas at a southwest Florida and a northeast Florida location: implications for leaf litter processing. Estuaries 18:591–597

    Article  Google Scholar 

  • McNeill SE, Worthington DG, Ferrell DJ, Bell JD (2006) Consistently outstanding recruitment of five species of fish to a seagrass bed in Botany Bay, NSW. Aust J Ecol 17:359–365

    Article  Google Scholar 

  • Melville AJ, 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 

  • Meyer DL, Johnson JM, Gill JW (2001) Comparison of nekton use of Phragmites australis and Spartina alterniflora marshes in the Chesapeake Bay, USA. Mar Ecol Prog Ser 209:71–84

    Article  Google Scholar 

  • Meyneke J-O, Lee SY, Duke NC (2008a) Linking spatial metrics and fish catch reveals the importance of coastal wetland connectivity to inshore fisheries in Queensland, Australia. Biol Conserv 141:981–996

    Article  Google Scholar 

  • Meyneke J-O, Poole GC, Werry J, Lee SY (2008b) Use of PIT tag and underwater video recording in assessing estuarine fish movement in a high intertidal mangrove and salt marsh creek. Estuar Coast Shelf Sci 79:168–178

    Article  Google Scholar 

  • Minello TJ, Webb JW (1997) Use of natural and created Spartina alterniflora salt marshes by fishery species and other aquatic fauna in Galveston Bay, Texas, USA. Mar Ecol Prog Ser 151:165–179

    Article  Google Scholar 

  • Minello TJ, Zimmerman RJ (1992) Utilization of natural and transplanted Texas salt marshes by fish and decapod crustaceans. Mar Ecol Prog Ser 90:273–285

    Article  Google Scholar 

  • Minello TJ, Zimmerman RJ, Medina R (1994) The importance of edge for natant macrofauna in a created salt marsh. Wetlands 14:184–198

    Article  Google Scholar 

  • Minello TJ, Able KW, Weinstein MP, 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

    Article  Google Scholar 

  • Minello TJ, Rozas LP, Baker R (2012) Geographic variability in salt marsh flooding patterns may affect nursery value for fishery species. Estuar Coast 35:501–514

    Article  CAS  Google Scholar 

  • Morton RM (1990) Community structure, density and standing crop of fishes in a subtropical Australian mangrove area. Mar Biol 105:385–394

    Article  Google Scholar 

  • Morton RM, Pollock BR, Beumer JP (1987) The occurrence and diet of fishes in a tidal inlet to a saltmarsh in southern Moreton Bay, Queensland. Aust J Ecol 12:217–237

    Article  Google Scholar 

  • Nagelkerken I, Faunce CH (2008) What makes mangroves attractive to fish? Use of artificial units to test the influence of water depth, cross-shelf location, and presence of root structure. Estuar Coast Shelf Sci 79:559–565

    Article  Google Scholar 

  • Nagelkerken I, van der Velde G, Gorissen MW, Meijer GJ, van’t Hof T, den Hartog C (2000) Importance of mangroves, seagrass beds and the shallow coral reef as a nursery for important coral reef fishes, using a visual census technique. Estuar Coast Shelf Sci 51:31–44

    Article  Google Scholar 

  • Nagelkerken I, Blaber SJM, Bouillon S, Green P, Haywood M, Kirton LG, Meyneke J-O, Pawlik J, Penrose HM, Sasekumar A, Somerfield PJ (2008) The habitat function of mangroves for terrestrial and marine fauna: a review. Aquat Bot 89:155–185

    Article  Google Scholar 

  • Nakamura Y, Horinouchi M, Shibuno T, Tanaka Y, Miyajima T, Koike I, Kurokura H, Sano M (2008) Evidence of ontogenetic migration from mangroves to coral reefs by black-tail snapper Lutjanus fulvus: stable isotope approach. Mar Ecol Prog Ser 355:257–266

    Article  Google Scholar 

  • Nanjo K, Hiroyoshi K, Sano M (2008) Food habits of fishes in the mangrove estuary of Urauchi River, Iriomote Island, southern Japan. Fish Sci 74:1024–1033

    Article  CAS  Google Scholar 

  • Nemerson DM, Able KW (2004) Spatial patterns in diet and distribution of juveniles of four fish species in Delaware Bay marsh creeks: factors influencing fish abundance. Mar Ecol Prog Ser 276:249–262

    Article  Google Scholar 

  • Nordlie FG (2003) Fish communities of estuarine salt marshes of eastern North America, and comparisons with temperate estuaries of other continents. Rev Fish Biol Fish 13:281–325

    Article  Google Scholar 

  • Nordlie FG (2006) Physicochemical environments and tolerances of cyprinodontoid fishes found in estuaries and salt marshes of eastern North America. Rev Fish Biol Fish 16:51–106

    Article  Google Scholar 

  • Odum WE (1988) Comparative ecology of tidal freshwater and salt marshes. Ann Rev Ecol Syst 19:147–176

    Article  Google Scholar 

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

    Article  Google Scholar 

  • Orth RJ, Carruthers TJB, Dennison WC, Duarte CM, Fourqurean JW, Hecj KL, Hughes AR, Kendrick GA, Kenworthy WJ, Olyarnik S, Short FT, Waycott M, Williams SL (2006) A global crisis for seagrass ecosystems. BioSci 56:987–996

    Article  Google Scholar 

  • Paterson AW (1998) Aspects of the ecology of fishes associated with salt marshes and adjacent habitats in a temperate South African estuary. PhD thesis, Rhodes University, Grahamstown

  • Paterson AW, Whitfield AK (1996) The fishes associated with an intertidal salt marsh creek in the Kariega Estuary, South Africa. Trans R Soc S Afr 51:195–218

    Article  Google Scholar 

  • Paterson AW, Whitfield AK (1997) A stable carbon isotope study of the food-web in a freshwater-deprived South African estuary, with particular emphasis on the ichthyofauna. Estuar Coast Shelf Sci 45:705–715

    Article  Google Scholar 

  • Paterson AW, Whitfield AK (2000a) Do shallow-water habitats function as refugia for juvenile fishes? Estuar Coast Shelf Sci 51:359–364

    Article  Google Scholar 

  • Paterson AW, Whitfield AK (2000b) The ichthyofauna associated with an intertidal creek and adjacent eelgrass beds in the Kariega Estuary, South Africa. Environ Biol Fish 58:145–156

    Article  Google Scholar 

  • Paterson AW, Whitfield AK (2003) The fishes associated with three intertidal salt marsh creeks in a temperate South African estuary. Wetl Ecol Manag 11:305–315

    Article  Google Scholar 

  • Penhale PA (1977) Macrophyte-epiphyte biomass and productivity in an eelgrass (Zostera marina L.) community. J Exp Mar Biol Ecol 26:221–224

    Article  Google Scholar 

  • Peterson MS, Lowe MR (2009) Implications of cumulative impacts to estuarine and marine habitat quality for fish and invertebrate resources. Rev Fish Sci 17:505–523

    Article  Google Scholar 

  • Peterson GW, Turner RF (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

    Article  Google Scholar 

  • Phelan BA, Goldberg R, Bejda AJ, Pereira J, Hagan S, Clark P, Studholme AL, Calabrese A, 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  CAS  PubMed  Google Scholar 

  • Pihl L, Cattrijsse A, Codling I, Mathieson S, McLusky DS, Roberts C (2002) Habitat use by fishes in estuaries and other brackish areas. In: Elliott M, Hemingway KL (eds) Fishes in estuaries. Blackwell Science, Oxford, pp 10–53

    Chapter  Google Scholar 

  • Pihl L, Baden S, Kautsky N, Rönnbäck P, Söderqvist T, Troell M, Wennhage H (2006) Shift in fish assemblage structure due to loss of seagrass Zostera marina habitats in Sweden. Estuar Coast Shelf Sci 67:123–132

    Article  Google Scholar 

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

    Article  Google Scholar 

  • Pittman SJ, McAlpine CA, Pittman KM (2004) Linking fish and prawns to their environment: a hierarchical landscape approach. Mar Ecol Prog Ser 283:233–254

    Article  Google Scholar 

  • Pollard DA (1984) A review of ecological studies on seagrass-fish communities, with particular reference to recent studies in Australia. Aquat Bot 18:3–42

    Article  Google Scholar 

  • Polte P, Asmus H (2006) Influence of seagrass beds (Zostera noltii) on the species composition of juvenile fishes temporarily visiting the intertidal zone of the Wadden Sea. J Sea Res 55:244–252

    Article  Google Scholar 

  • Potter IC, Tweedley JR, Elliott M, Whitfield AK (2015) The ways in which fish use estuaries: a refinement and expansion of the guild approach. Fish Fish 16:230–239

    Article  Google Scholar 

  • Potthoff MT, Allen DM (2003) Site fidelity, home range, and tidal migrations of juvenile pinfish, Lagodon rhomboides, in salt marsh creeks. Env Biol Fish 67:231–240

    Article  Google Scholar 

  • Primavera JH (1997) Fish predation on mangrove-associated penaeids: the role of structures and substrate. J Exp Mar Biol Ecol 215:205–216

    Article  Google Scholar 

  • Rakocinski CF, Baltz DM, Fleeger JW (1992) Correspondence between environmental gradients and the community structure of marsh-edge fishes in a Louisiana estuary. Mar Ecol Prog Ser 80:135–148

    Article  Google Scholar 

  • Raposa KB, Roman CT (2001) Seasonal habitat-use patterns of nekton in a tide-restricted and unrestricted New England salt marsh. Wetlands 21:451–461

    Article  Google Scholar 

  • Raposa KB, Roman CT (2003) Using gradients in tidal restriction to evaluate nekton community responses to salt marsh restoration. Estuaries 26:98–105

    Article  Google Scholar 

  • Ray GC (2005) Connectivities of estuarine fishes to the coastal realm. Estuar Coast Shelf Sci 64:18–32

    Article  Google Scholar 

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

    Article  Google Scholar 

  • Robertson AI, Duke NC (1990) Recruitment, growth and residence time of fishes in a tropical Australian mangrove system. Estuar Coast Shelf Sci 31:723–743

    Article  Google Scholar 

  • Rogers SG, Targett TE, van Sant SB (1984) Fish-nursery use in Georgia salt-marsh estuaries: the influence of springtime freshwater conditions. Trans Am Fish Soc 113:595–606

    Article  Google Scholar 

  • Rönnbäck P, Troell M, Kautsky N, Primavera JH (1999) Distribution pattern of shrimps and fish among Avicennia and Rhizophora microhabitats in the Pagbilao mangroves, Phillipines. Estuar Coast Shelf Sci 48:223–234

    Article  Google Scholar 

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

    Article  Google Scholar 

  • Rooker JR, Holt SA, Holt GJ (1998b) 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 

  • Rotherham D, West RJ (2002) Do different seagrass species support distinct fish communities in south-eastern Australia? Fish Manag Ecol 9:235–248

    Article  Google Scholar 

  • Rountree RA, Able KW (1992) Fauna of polyhaline salt marsh creeks in southern New Jersey: composition, abundance and biomass. Estuaries 15:171–185

    Article  Google Scholar 

  • Rountree RA, Able KW (1993) Diel variation in decapod crustacean and fish assemblages in New Jersey polyhaline salt marsh creeks. Estuar Coast Shelf Sci 37:181–201

    Article  Google Scholar 

  • Rountree RA, Able KW (2007) Spatial and temporal habitat use patterns for salt marsh nekton: implications for ecological functions. Aquat Ecol 41:25–45

    Article  CAS  Google Scholar 

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

    Article  Google Scholar 

  • Rozas LP, Hackney CT (1984) Use of oligohaline marshes by fishes and macrofaunal crustaceans in North Carolina. Estuaries 7:213–224

    Article  Google Scholar 

  • Rozas LP, 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 

  • Rozas LP, Odum WE (1987) Use of tidal freshwater marshes by fishes and macrofaunal crustaceans along a marsh stream-order gradient. Estuaries 10:36–43

    Article  Google Scholar 

  • Rozas LP, Odum WE (1988) Occupation of submerged aquatic vegetation by fishes: testing the roles of food and refuge. Oecologia 77:101–106

    Article  Google Scholar 

  • Saintilan N, Hossain K, Mazumder D (2007) Linkages between seagrass, mangrove and saltmarsh as fish habitat in the Botany Bay estuary, New South Wales. Wetl Ecol Manag 15:277–286

    Article  Google Scholar 

  • Salgado JP, Cabral HN, Costa MJ, Deegan L (2004) Nekton use of salt marsh creeks in the upper Tejo Estuary. Estuaries 27:818–825

    Article  Google Scholar 

  • Sanchez-Jerez P, Gillanders BM, Kingsford MJ (2002) Spatial variability of trace elements in fish otoliths: comparison with dietary items and habitat constituents in seagrass meadows. J Fish Biol 61:801–821

    Article  CAS  Google Scholar 

  • Sardá R, Foreman K, Werme CE, Valiela I (1998) The impact of epifaunal predation on the structure of macrofaunal invertebrate communities of tidal saltmarsh creeks. Estuar Coast Shelf Sci 46:657–669

    Article  Google Scholar 

  • Sasekumar A, Chong VC, Leh MU, D’Cruz R (1992) Mangroves as a habitat for fish and prawns. Hydrobiol 247:195–207

    Article  Google Scholar 

  • Schleyer MH, Roberts GA (1987) Detritus cycling in a shallow coastal lagoon in Natal, South Africa. J Exp Mar Biol Ecol 110:27–40

    Article  Google Scholar 

  • Sheaves M (2005) Nature and consequences of biological connectivity in mangrove systems. Mar Ecol Prog Ser 302:293–305

    Article  Google Scholar 

  • Sheaves M (2009) Consequences of ecological connectivity: the coastal ecosystem mosaic. Mar Ecol Prog Ser 391:107–115

    Article  Google Scholar 

  • Sheaves M, Molony B (2000) Short-circuit in the mangrove food chain. Mar Ecol Prog Ser 199:97–109

    Article  Google Scholar 

  • Sheaves M, Baker R, Johnston R (2006) Marine nurseries and effective juvenile habitats: an alternative view. Mar Ecol Prog Ser 318:303–306

    Article  Google Scholar 

  • Shenker JM, Dean JM (1979) The utilization of an intertidal salt marsh creek by larval and juvenile fishes: abundance, diversity and temporal variation. Estuaries 2:154–163

    Article  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, Hayes C (2003) Are mangroves nursery habitat for transient fishes and decapods? Wetlands 23:449–458

    Article  Google Scholar 

  • Shervette VR, Aguirre WE, Blacio E, Cevallos R, Gonzalez M, Pozo F, Gelwick F (2007) Fish communities of a disturbed mangrove wetland and an adjacent tidal river in Palmar, Ecuador. Estuar Coast Shelf Sci 72:115–128

    Article  Google Scholar 

  • Short FT, Wyllie-Echeverria S (1996) Natural and human-induced disturbance of seagrasses. Environ Conserv 23:17–27

    Article  Google Scholar 

  • Smith KJ, Able KW (1994) Salt-marsh tide pools as winter refuges for the mummichog, Fundulus heteroclitus, in New Jersey. Estuaries 17:226–234

    Article  CAS  Google Scholar 

  • Smith KJ, Able KW (2003) Dissolved oxygen dynamics in salt marsh pools and its potential impacts on fish assemblages. Mar Ecol Prog Ser 258:223–232

    Article  CAS  Google Scholar 

  • Smith KA, Sinerchia M (2004) Timing of recruitment events, residence periods and post-settlement growth of juvenile fish in a seagrass nursery area, south-eastern Australia. Env Biol Fish 71:73–84

    Article  Google Scholar 

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

    Article  Google Scholar 

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

    Article  Google Scholar 

  • Stoner AW (1983) Distribution of fishes in seagrass meadows: role of macrophyte biomass and species composition. Fish Bull 81:837–846

    Google Scholar 

  • Stoner AW, Zimmerman RJ (1988) Food pathways associated with penaeid shrimps in a mangrove-fringed estuary. Fish Bull 86:543–551

    Google Scholar 

  • Stunz GW, Levin PS, Minello TJ (2001) Selection of estuarine nursery habitats by wild-caught and hatchery-reared juvenile red drum in laboratory mesocosms. Env Biol Fish 61:305–313

    Article  Google Scholar 

  • Stunz GW, Minello TJ, Levin PS (2002a) A comparison of early juvenile red drum densities among various habitat types in Galveston Bay, Texas. Estuaries 25:76–85

    Article  Google Scholar 

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

    Article  Google Scholar 

  • Szedlmayer ST, Able KW (1996) Patterns of seasonal availability and habitat use by fishes and decapod crustaceans in a southern New Jersey estuary. Estuaries 19:697–709

    Article  Google Scholar 

  • Talbot CW, Able KW (1984) Composition and distribution of larval fishes in New Jersey high marshes. Estuaries 7:434–443

    Article  Google Scholar 

  • Tanaka Y (1991) Microbial decomposition of reed (Phragmites communis) leaves in a saline lake. Hydrobiol 220:119–129

    Article  CAS  Google Scholar 

  • Thayer GW, Colby DR, Hettler WF (1987) Utilisation of the red mangrove prop root habitat by fishes in south Florida. Mar Ecol Prog Ser 35:25–38

    Article  Google Scholar 

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

    Article  Google Scholar 

  • Tolan JM, Holtt SA, Onuf CP (1997) Distribution and community structure of ichthyoplankton in Laguna Madre seagrass meadows: potential impact of seagrass species change. Estuaries 20:450–464

    Article  Google Scholar 

  • Tse P, Nip THM, Wong CK (2008) Nursery function of mangrove: a comparison with mudflat in terms of fish species composition and fish diet. Estuar Coast Shelf Sci 80:235–242

    Article  Google Scholar 

  • Tupper M, Able KW (2000) Movements and food habits of striped bass (Morone saxatilis) in Delaware Bay (USA) salt marshes: comparison of a restored and a reference marsh. Mar Biol 137:1049–1058

    Article  Google Scholar 

  • Unsworth RKF, Bell JJ, Smith DJ (2007) Tidal fish connectivity of reef and sea grass habitats in the Indo-Pacific. J Mar Biol Ass UK 87:1287–1296

    Article  Google Scholar 

  • Unsworth RKF, De León PS, Garrard SL, Jompa J, Smith DJ, Bell JJ (2008) High connectivity of Indo-Pacific seagrass fish assemblages with mangrove and coral reef habitats. Mar Ecol Prog Ser 353:213–224

    Article  Google Scholar 

  • Unsworth RKF, Garrard SL, De León PS, Cullen LC, Smith DJ, Sloman KA, Bell JJ (2009) Structuring of Indo-Pacific fish assemblages along the mangrove-seagrass continuum. Aquat Biol 5:85–95

    Article  Google Scholar 

  • Uwe U, Ulrich S-P (2003) Observations of fish migration in a macrotidal mangrove channel in northern Brazil using a 200-kHz split-beam sonar. Aquat Living Resour 16:175–184

    Article  Google Scholar 

  • van Dam AA, Beveridge MCM, Azim ME, Verdegem MCJ (2002) The potential of fish production based on periphyton. Rev Fish Biol Fish 12:1–31

    Article  Google Scholar 

  • Vance DJ, Haywood MDE, Heales DS, Kenyon RA, Loneragan NR, Pendrey RC (1996) How far do prawns and fish move into mangroves? Distribution of juvenile banana prawns Penaeus merguiensis and fish in a tropical mangrove forest in northern Australia. Mar Ecol Prog Ser 131:115–124

    Article  Google Scholar 

  • Vasconcelos RP, Reis-Santos P, Tanner S, Maia A, Latkoczy C, Günther D, Costa MJ, Cabral H (2008) Evidence of estuarine nursery origin of five coastal fish species along the Portuguese coast through otolith elemental fingerprints. Estuar Coast Shelf Sci 79:317–327

    Article  Google Scholar 

  • Veiga P, Vieira L, Bexiga C, Sá R, Erzini K (2006) Structure and temporal variations of fish assemblages of the Castro Marim salt marsh, southern Portugal. Estuar Coast Shelf Sci 70:27–38

    Article  Google Scholar 

  • Vidy G (2000) Estuarine and mangrove systems and the nursery concept: which is which? The case of the Sine Saloum system (Senegal). Wetl Ecol Manag 8:37–51

    Article  Google Scholar 

  • Weerts SP, Cyrus DP (2002) Occurrence of young and small-sized fishes in different habitats within a subtropical South African estuary and adjacent harbour. Mar Freshw Res 53:447–456

    Article  Google Scholar 

  • Weinstein MP, Balletto JH (1999) Does the common reed, Phragmites australis, affect essential fish habitat. Estuaries 24:441–452

    Google Scholar 

  • Weinstein MP, Litvin SY, Bosley KL, Fuller CM, Wainwright SC (2000) The role of tidal marsh as an energy source for marine transient and resident finfishes: a stable isotope approach. Trans Am Fish Soc 129:797–810

    Article  Google Scholar 

  • Weinstein MP, Litvin SY, Guida VG (2010) Stable isotope and biochemical composition of white perch in a Phragmites dominated salt marsh and adjacent waters. Wetlands 30:1181–1191

    Article  Google Scholar 

  • Weis JS, Weis P (2003) Is the invasion of the common reed, Phragmites australis, into tidal marshes of the eastern US an ecological disaster? Mar Poll Bull 46:816–820

    Article  CAS  Google Scholar 

  • Werner EE, Gilliam JF, Hall DJ, Mittelbach GG (1983) An experimental test of the effects of predation risk on habitat use in fish. Ecology 64:1540–1548

    Article  Google Scholar 

  • West JM, Zedler JB (2000) Marsh-creek connectivity: fish use of a tidal salt marsh in southern California. Estuaries 23:699–710

    Article  Google Scholar 

  • Whitfield AK (1980) A quantitative study of the trophic relationships within the fish community of the Mhlanga estuary, South Africa. Est Coast Mar Sci 10:417–435

    Article  Google Scholar 

  • Whitfield AK (1984) The effects of prolonged aquatic macrophyte senescence on the biology of the dominant fish species in a southern African coastal lake. Estuar Coast Shelf Sci 18:315–329

    Article  Google Scholar 

  • Whitfield AK (1988a) The Swartvlei estuary fish community and the influence of food availability on resource utilization. Estuaries 11:160–170

    Article  Google Scholar 

  • Whitfield AK (1988b) The role of tides in redistributing macrodetrital aggregates within the Swartvlei estuary. Estuaries 11:152–159

    Article  Google Scholar 

  • Whitfield AK, Pattrick P (2015) Habitat type and nursery function for coastal marine fish species, with emphasis on the Eastern Cape region, South Africa. Estuar Coast Shelf Sci 160:49–59

    Article  Google Scholar 

  • Whitfield AK, Beckley LE, Bennett BA, Branch GM, Kok HM, Potter IC, van der Elst RP (1989) Composition, species richness and similarity of ichthyofaunas in eelgrass Zostera capensis beds of southern Africa. S Afr J Mar Sci 8:251–259

    Article  Google Scholar 

  • Whitfield AK, James NC, Lamberth SJ, Adams JB, Perissinotto R, Rajkaran A, Bornman T (2016) The role of pioneers as indicators of biogeographic range expansion caused by global change in southern African coastal waters. Estuar Coast Shelf Sci 172:138–153

    Article  Google Scholar 

  • Wiegert RG, Pomeroy LR (1981) The salt-marsh ecosystem: a synthesis. In: Wiegert RG, Pomeroy LR (eds) The ecology of a salt marsh. Springer, New York, pp 219–230

    Chapter  Google Scholar 

  • Yáñez-Arancibia A, Lara-Dominguez AL, Rojas-Galaviz JL, Sånchez-Gil P, Day JW, Madden CJ (1988) Seasonal biomass and diversity of estuarine fishes coupled with tropical habitat heterogeneity (southern Gulf of Mexico). J Fish Biol 33:191–200

    Article  Google Scholar 

  • Yáñez-Arancibia A, Lara-Dominguez AL, Day JW (1993) Interactions between mangrove and seagrass habitats mediated by estuarine nekton assemblages: coupling of primary and secondary production. Hydrobiol 264:1–12

    Article  Google Scholar 

  • York PH, Booth DJ, Glasby TM, Pease BC (2006) Fish assemblages in habitats dominated by Caulerpa taxifolia and native seagrasses in south-eastern Australia. Mar Ecol Prog Ser 312:223–234

    Article  Google Scholar 

Download references

Acknowledgements

I thank Elaine Heemstra for the use of fish illustrations shown in Fig. 1 and the National Research Foundation (NRF) for financial support. I am also grateful to Janine Adams and two referees for their useful comments regarding earlier versions of this manuscript.

Author information

Authors and Affiliations

Authors

Corresponding author

Correspondence to Alan K. Whitfield.

Rights and permissions

Reprints and permissions

About this article

Check for updates. Verify currency and authenticity via CrossMark

Cite this article

Whitfield, A.K. The role of seagrass meadows, mangrove forests, salt marshes and reed beds as nursery areas and food sources for fishes in estuaries. Rev Fish Biol Fisheries 27, 75–110 (2017). https://doi.org/10.1007/s11160-016-9454-x

Download citation

  • Received:

  • Accepted:

  • Published:

  • Issue Date:

  • DOI: https://doi.org/10.1007/s11160-016-9454-x

Keywords

Navigation