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Differences in fish assemblage structures between fragmented and continuous seagrass beds in Trang, southern Thailand

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Abstract

Fish assemblage structures in fragmented and continuous seagrass habitats in Trang Province, Thailand, were examined in detail to elucidate the effects of habitat fragmentation. The assemblage structures clearly differed: fish species diversity was apparently higher in the fragmented seagrass beds, although total fish numbers did not differ between them. A total of 37 fish species were collected, including 24 and 34 species from the continuous and fragmented beds, respectively. Thirteen species were restricted to the fragmented beds, compared with three restricted to the continuous beds. In addition, eight species were more abundant in the fragmented beds and only two in the continuous beds. Such differences may have arisen, at least in part, from differences in microhabitat diversity and the relative amounts of microhabitats between the two habitat types, as well as specific microhabitat preferences of the resident fishes. Although fragmented beds supported greater fish species diversity at the present study sites, it is axiomatic that habitat fragmentation caused by anthropogenic disturbance is unacceptable, with seagrass-habitat conservation being essential for both the preservation of high overall biodiversity and the successful management of local fisheries.

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References

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

    Article  Google Scholar 

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

    Google Scholar 

  3. 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 

  4. Sogard SM (1989) 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 

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

    Article  Google Scholar 

  6. Edgar GJ, Shaw C (1995) 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 

  7. Nakamura Y, Tsuchiya M (2008) Spatial and temporal patterns of seagrass habitat use by fishes at the Ryukyu Islands, Japan. Estuar Coast Shelf Sci 76:345–356

    Article  Google Scholar 

  8. Horinouchi M (2007) Review of the effects of within-patch scale structural complexity on seagrass fishes. J Exp Mar Biol Ecol 350:111–129

    Article  Google Scholar 

  9. Sano M, Nakamura Y, Shibuno T, Horinouchi M (2008) Are seagrass beds and mangroves in the tropics nursery habitats for many fish species? (in Japanese). Nippon Suisan Gakkai Shi 74:93–96

    Google Scholar 

  10. Shepard SA, McComb AJ, Bulthius DA, Neverauska V, Steffensen DA, West R (1989) Decline of seagrasses. In: Larkum AWD, McComb AJ, Shepard SA (eds) Biology of seagrasses: a treatise on seagrass with special reference to the Australian region. Elsevier, Amsterdam, pp 346–393

    Google Scholar 

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

    Article  Google Scholar 

  12. Hauxwell J, Cebriàn J, Valiela I (2003) Eelgrass Zostera marina loss in temperate estuaries: relationship to land-derived nitrogen loads and effect of light limitation imposed by algae. Mar Ecol Prog Ser 247:59–73

    Article  CAS  Google Scholar 

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

    Article  Google Scholar 

  14. Jackson EL, Rowden AA, Attrill MJ, Bossy SF, Jones MB (2002) Comparison of fish and mobile macroinvertebrates associated with seagrass and adjacent sand at St. Catherine Bay, Jersey (English Channel): emphasis on commercial species. Bull Mar Sci 71:1333–1341

    Google Scholar 

  15. Horinouchi M (2005) A comparison of fish assemblages from seagrass beds and the adjacent bare substrata in Lake Hamana, central Japan. Laguna 12:69–72

    Google Scholar 

  16. Horinouchi M (2009) Horizontal gradient in fish assemblage structures in and around a seagrass habitat: some implications for seagrass habitat conservation. Ichthyol Res 56:109–125

    Article  Google Scholar 

  17. Kimura S, Matsuura K (2003) Fishes of Bitung, northern tip of Sulawesi, Indonesia. Ocean Research Institute. University of Tokyo, Tokyo

    Google Scholar 

  18. Matsuura K, Kimura S (2005) Fishes of Libong Island, wet coast of southern Thailand. Ocean Research Institute. University of Tokyo, Tokyo

    Google Scholar 

  19. Fahrig L (2003) Effects of habitat fragmentation on biodiversity. Annu Rev Ecol Evol Syst 34:487–515

    Article  Google Scholar 

  20. Garrison BA (2005) Fragmentation of terrestrial habitat: an overview for wildlife biologists. Trans W Sect Wildl Soc 41:42–58

    Google Scholar 

  21. Saunders DA, Hobbs RJ, Margules CR (1991) Biological consequences of ecosystem fragmentation. A review. Conserv Biol 5:18–32

    Article  Google Scholar 

  22. Fagan WE, Cantrell RS, Cosner C (1999) How habitat edges change species interactions. Am Nat 153:165–182

    Article  Google Scholar 

  23. Laurel B, Gregory RS, Brown JA (2003) Predator distribution and habitat patch area determined predation rates of age-0 juvenile cod Gadus spp. Mar Ecol Prog Ser 251:245–254

    Article  Google Scholar 

  24. Horinouchi M, Mizuno N, Jo Y, Fujita M, Sano M, Suzuki Y (2009) Seagrass habitat complexity does not always decrease foraging efficiencies of piscivorous fishes. Mar Ecol Prog Ser 377:43–49

    Article  Google Scholar 

  25. Horinouchi M, Sano M (2001) Effects of changes in seagrass shoot density and leaf height on the abundance of juveniles of Acentrogobius pflaumii in a Zostera marina bed. Ichthyol Res 48:179–185

    Article  Google Scholar 

  26. Horinouchi M (2007) Distribution patterns of benthic juvenile gobies in and around seagrass habitats: effectiveness of seagrass shelter against predators. Estuar Coast Shelf Sci 72:657–664

    Article  Google Scholar 

  27. Breitburg DL, Palmer MA, Loher T (1995) Larval distributions and the spatial patterns of settlement of an oyster reef fish: responses to flow and structure. Mar Ecol Prog Ser 125:45–60

    Article  Google Scholar 

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Acknowledgments

We are grateful to Yukinori Nakane, Koji Fujimoto, Suwat Tanyaros, Suwana Taveepattanapong, and the staff of the Faculty of Science and Fisheries Technology, Rajamangala University of Technology Srivijaya for their generous assistance in the field work, and Ai Yoshizawa and Sachi Sugiura for their helpful suggestions in fish identification. Constructive comments on the manuscript from Graham Hardy and anonymous referees were much appreciated. This work was conducted with the permission of the National Research Council of Thailand and was financially supported by a Grant-in-Aid for Scientific Research (B) from the Ministry of Education, Science, Sports and Culture of Japan (No. 19405032).

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Correspondence to Masahiro Horinouchi.

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Horinouchi, M., Tongnunui, P., Nanjyo, K. et al. Differences in fish assemblage structures between fragmented and continuous seagrass beds in Trang, southern Thailand. Fish Sci 75, 1409–1416 (2009). https://doi.org/10.1007/s12562-009-0166-1

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