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Marine Biology

, Volume 150, Issue 1, pp 141–148 | Cite as

Life history and reproduction of the amphipod Synchelidium trioostegitum (Crustacea, Oedicerotidae) on a sandy shore in Korea

  • Ok Hwan Yu
  • Hae-Lip Suh
Research Article

Abstract

The life history and reproductive strategy of the amphipod Synchelidium trioostegitum were studied on a sandy shore at Dolsando, South Korea. Samples were taken once a month for 1 year using a 0.3-mm sledge net on the bottom in 1 m of water at spring tide low water. The highest density of S. trioostegitum occurred from February through March. Ovigerous females were recorded virtually year-round, with a particularly high proportion in fall and early spring, indicating continuous recruitment with two dominant periods. The occurrence of ovigerous females was not correlated with environmental factors, such as temperature and salinity, and no significant difference between the body lengths of females and males was observed. The mean adult body length was greater in the early spring breeding period than in the fall. Brood size and embryo volume were positively correlated with the body length of ovigerous females. Brood size significantly decreased with increases in embryonic developmental stage. Embryo volume was significantly larger in the fall than in the early spring, but brood size was significantly smaller in fall, suggesting a strategy of using the same amount of reproductive energy during breeding periods. This type of reproductive effort is different from that of other Synchelidium amphipods having the same habitat and feeding regime. Our results suggest that interspecific competition for food and territory may be important in defining the reproductive strategy.

Keywords

Body Length Brood Size Breeding Period Ovigerous Female Life History Pattern 
These keywords were added by machine and not by the authors. This process is experimental and the keywords may be updated as the learning algorithm improves.

Notes

Acknowledgments

We thank Dr. B. Sainte-Marie (Maurice Lamontagne Institute, Fisheries and Oceans Canada, Canada) and Dr. K.E. Conlan (Canadian Museum of Nature, Canada) for critical readings of the manuscript and providing valuable comments. We also thank two reviewers for their valuable comments that greatly improved the manuscript. This work has been conducted with the support through the research program of KORDI with contract Nos. PE97201 and PP06401.

References

  1. Beare DJ, Moore PG (1996) The distribution, growth and reproduction of Pontocrates arenarius and P. altamarinus (Crustacea: Amphipoda) at Millport, Scotland. J Mar Biol Assoc UK 76:931–950CrossRefGoogle Scholar
  2. Beare DJ, Moore PG (1998a) Aspects of the life histories of Perioculodes longimanus, Pontocrates arcticus and Synchelidium maculatum (Crustacea: Amphipoda) at Millport, Scotland. J Mar Biol Assoc UK 78:193–209CrossRefGoogle Scholar
  3. Beare DJ, Moore PG (1998b) The life history of the offshore Oedicerotids Westwoodilla caecula and Monoculodes packardi (Crustacea: Amphipoda) from Loch fine, Scotland. J Mar Biol Assoc UK 78:835–852CrossRefGoogle Scholar
  4. Bell MC, Fish JD (1996) Fecundity and seasonal changes in reproductive output of females of the gravel beach amphipod, Pectenogammarus planicrurus. J Mar Biol Assoc UK 76:37–55CrossRefGoogle Scholar
  5. Conlan KE (1994) Amphipod crustaceans and environmental disturbance: a review. J Nat Hist 28:519–554CrossRefGoogle Scholar
  6. Cunha MR, Moreira MH, Sorbe JC (2000) Predicting amphipods brood size variation in brackish environments: an empirical model for Corophium multisetosum Stock, 1952 (Corophiidae) in Ria de Aveiro (NW Portugal). J Exp Mar Biol Ecol 248:207–223CrossRefGoogle Scholar
  7. Donn TE, Croker RA (1983) Production ecology of Haustorius Canadensis (Amphipoda: Haustoriidae) in Southern Maine. In: McLachlan A, Erasmus T (eds) Sandy beaches as ecosystems. Junk Publications, Hague, pp 661–667CrossRefGoogle Scholar
  8. Donn TE, Croker RA (1986) Life-history patterns of Haustorius Canadensis (Crustacea: Amphipoda) in northern New England. Can J Zool 64:99–104CrossRefGoogle Scholar
  9. Fenwick GD (1984) Life-history tactics of brooding crustacean. J Exp Mar Biol Ecol 84:247–264CrossRefGoogle Scholar
  10. Fish JD (1975) Development, hatching and brood size in Bathyporeia pilosa and B. pelagica (Crustacea: Amphipoda). J Mar Biol Assoc UK 55:357–368CrossRefGoogle Scholar
  11. Fish JD, Mills A (1979) The reproductive biology of Corophium volutator and C. arenarium (Crustacea: Amphipoda). J Mar Biol Assoc UK 59:355–368CrossRefGoogle Scholar
  12. Gomez J, Defeo O (1999) Life history of the sandhopper Pseudorchestoidea brasiliensis (Amphipoda) in sandy beaches with contrasting morphodynamics. Mar Ecol Prog Ser 182:209–220CrossRefGoogle Scholar
  13. Gouvis N, Kevrekidis T, Koukouras A (1997) Temporal changes of a macrobenthic assemblage in Evros delta (north Aegean Sea). Internat. Rev Gesamte Hydrobiol 82:67–80CrossRefGoogle Scholar
  14. Hughes JE (1982) Life history of the sandy-beach amphipod Dogielinotus loquax (Crustacea: Dogielinotidae) from the outer coast of Washington, USA. Mar Biol 71:167–175CrossRefGoogle Scholar
  15. Jo YW (1990) Taxonomy and biogeography of sandy beach Amphipoda (Crustacea) of Korea. PhD Thesis, University of AmsterdamGoogle Scholar
  16. Kevrekidis T (1997) Seasonal variation of the macrobenthic fauna in an isolated area of the Evros delta (north Aegean sea). Israel J Zool 43:243–255Google Scholar
  17. Kolding S, Fenchel TM (1981) Patterns of reproduction in different populations of five species of the amphipod genus Gammarus. Oikos 37:167–172CrossRefGoogle Scholar
  18. Moore PG (1981) The life histories of the amphipods Lembos websteri Bate and Corophium bonnellii Milne Edwards in kelp Holdfasts. J Exp Mar Biol Ecol 49:1–50CrossRefGoogle Scholar
  19. Moore PG, Wong YM (1996) Observations on the life history of Orchomene nanus (Kroyer) (Amphipoda: Lysianassoidea) at Millport, Scotland as deduced from baited trapping. J Exp Mar Biol Ecol 195:53–70CrossRefGoogle Scholar
  20. Nelson WG (1979) An analysis of structural pattern in an eelgrass (Zostera marina L.) amphipod community. J Exp Mar Biol Ecol 39:231–264CrossRefGoogle Scholar
  21. Nelson WG (1980) Reproductive patterns of Gammaridean amphipods. Sarsia 65:61–71CrossRefGoogle Scholar
  22. Rajagopal S, van der Velde G, Paffen BGP, van den Brink FWB, Bij de Vaate A (1999) Life history and reproductive biology of the invasive amphipod Corophium curvispinum (Crustacea: Amphipoda) in the Lower Rhine. Arch Hydrobiol 144:305–325CrossRefGoogle Scholar
  23. Sainte-Marie B (1991) A review of the reproductive bionomics of aquatic gammaridean amphipods: variation of life history traits with latitude, depth, salinity and superfamily. Hydrobiologia 223:189–227CrossRefGoogle Scholar
  24. Sainte-Marie B, Lamarche G, Gagnon J-M (1990) Reproductive bionomics of some shallow-water lysianassoids in the Saint Lawrence estuary, with a review of the fecundity of the Lysianassoidea (Crustacea, Amphipoda). Can J Zool 68:1639–1644CrossRefGoogle Scholar
  25. Segerstrale SG (1970) Light control of the reproductive cycle of Pontoporeia affinis Lindstrom (Crustacea, Amphipoda). J Exp Mar Biol Ecol 5:272–275CrossRefGoogle Scholar
  26. Seon SG (2001) Taxonomy and ecology of harpacticoid copepods in the intertidal zone of sandy shore, southern Korea. MSc Thesis, Chonnam National University, (http://www.168.131.53.98/cnud/CNU_005/425910.pdf)Google Scholar
  27. Sheader M (1978) Distribution and reproductive biology of Corophium insidiosum (Amphipoda) on the north-east coast of England. J Mar Biol Assoc UK 58:585–596CrossRefGoogle Scholar
  28. Sheader M (1983) The reproductive biologoy and ecology of Gammarus duebeni (Crustacea: Amphipoda) in southern England. J Mar Biol Assoc UK 63:517–540CrossRefGoogle Scholar
  29. Slattery PN (1985) Life histories of infaunal amphipods from subtidal sands of Monterey Bay, California. J Crustac Biol 5:635–649CrossRefGoogle Scholar
  30. Steele DH, Steele VJ (1975) The biology of Gammarus (Crustacea, Amphipoda) in the northwestern Atlantic. XI. Comparison and discussion. Can J Zool 53:1116–1126CrossRefGoogle Scholar
  31. Steele DH, Steele VJ (1991) Morphological and environmental restraints on egg production in amphipods. In: Wenner A, Kuris A (eds) Crustracean egg producion. Balkema, Netherlands, pp 157–170Google Scholar
  32. Thiel M (1998) Population biology of Dyopedos monacanthus (Crustacea: Ampipoda) on estuarine soft-bottoms: importance of extended parental care and pelagic movements. Mar Biol 132:209–221CrossRefGoogle Scholar
  33. Van Dolah RF, Bird E (1980) A comparison of reproductive patterns in epifaunal and infaunal Gammaridean amphipods. Estuar Coast Mar Sci 11:593–604CrossRefGoogle Scholar
  34. Williams JA (1978) The annual pattern of reproduction of Talitrus saltator (Crustacea: Amphiopoda: Talitridae). Zool Lond 184:231–244CrossRefGoogle Scholar
  35. Yu OH, Soh HY, Suh H-L (2002a) Life history and reproduction of Synchelidium lenorostralum (Amphipoda, Oedicerotidae) in a temperate sandy shore, southern Korea. J Crustac Biol 22:126–134CrossRefGoogle Scholar
  36. Yu OH, Soh HY, Suh H-L (2002b) Seasonal zonation patterns of benthic amphipods in a sandy shore surf zone of Korea. J Crustac Biol 22:459–466CrossRefGoogle Scholar
  37. Yu OH, Suh H-L, Shirayama Y (2003) Feeding ecology of three amphipod species Synchelidium lenorostralum, S. trioostegitum and Gitanopsis japonica in the surf zone of a sandy shore. Mar Ecol Prog Ser 258:189–199CrossRefGoogle Scholar

Copyright information

© Springer-Verlag 2006

Authors and Affiliations

  1. 1.Marine Ecosystem & Conservation Research Division, Marine Environment Research DepartmentKorea Ocean Research & Development InstituteSeoulRepublic of Korea
  2. 2.Institute of Marine Science, Faculty of Earth Systems and Environmental SciencesChonnam National UniversityGwangjuRepublic of Korea

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