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Life History and Morphological Responses of Daphnia similis against Chemical Compounds Exuded by Various Cohabiting Animals and Triops longicaudatus in the Rice Paddy Ecosystem

논 생태계에 서식하는 생물과 긴꼬리투구새우가 분비한 화학물질이 물벼룩의 생활사와 형태에 미치는 영향

  • La, Geung-Hwan (Department of Environmental Education, Sunchon National University) ;
  • Han, Eun-Jin (Department of Environmental Education, Sunchon National University) ;
  • Won, Doo Hee (Doohee Institute of Ecological Research (DIER), Korea Ecosystem Service Inc.) ;
  • Kim, Jeong-Hui (Department of Environmental Education, Sunchon National University) ;
  • Jeong, Jyoo-Ri (Department of Environmental Education, Sunchon National University) ;
  • Kim, Hyun-Woo (Department of Environmental Education, Sunchon National University)
  • 나긍환 (순천대학교 환경교육과) ;
  • 한은진 (순천대학교 환경교육과) ;
  • 원두희 ((주)생태조사단 부설 두희생태연구소) ;
  • 김정희 (순천대학교 환경교육과) ;
  • 정쥬리 (순천대학교 환경교육과) ;
  • 김현우 (순천대학교 환경교육과)
  • Received : 2015.10.29
  • Accepted : 2015.12.15
  • Published : 2015.12.31

Abstract

The aim of this study was to assess the interaction between Daphnia similis and various organisms related to the rice paddy ecosystem. We selected several organisms that are likely to prey on D. similis and evaluate predation rate as well as responses of D. similis to the chemical compounds exuded by these organisms. As a result of predation experiment, larval dragonfly (Anax parthenope) and Triops longicaudatus were clearly shown decreasing abundances of D. similis. Especially, Triops longicaudatus was observed higher feeding rates on D. similis than larval dragonfly. Chemical compounds from the vertebrates such as fish (Misgurnus anguillicaudatus, Pseudorasbora parva, Micropterus salmoides) and tadpole of frog (Rana nigromaculata) did not affect the life history of Daphnia. However, a potential predatory fish P. parva induced significantly longer tail spine in Daphnia. In addition, among the invertebrates (T. longicaudatus, A. Parthenope, Micronecta spp., Palaemon paucidens), chemical compounds exuded by T. longicaudatus induced shorter body and significantly longer tail spine in D. similis.

Keywords

References

  1. Alekseev, V.R., B.T. De Stasio and J.J. Gilbert. 2007. Diapause in aquatic invertebrates. theory and human use. Monographiae Biologicae.
  2. Asaeda, T., T. Priyadarshana and J. Manatunge. 2001. Effects of satiation on feeding and swimming behaviour of planktivores. Hydrobiologia 443: 147-157. https://doi.org/10.1023/A:1017560524056
  3. Beklioglu, M., M. Telli and A. Gozen. 2006. Fish and mucusdwelling bacteria interact to produce a kairomone that induces diel vertical migration in Daphnia. Freshwater Biology 51: 2200-2206. https://doi.org/10.1111/j.1365-2427.2006.01642.x
  4. Black, R.W. and N.G. Hairston. 1988. Predator driven changes in community structure. Oecologia 77: 468-479. https://doi.org/10.1007/BF00377262
  5. Boix, D., J. Sala, S. Gascon and S. Brucet. 2006. Predation in a temporary pond with special attention to the trophic role of Triops cancriformis (Crustacea: Branchiopoda: Notostraca). Hydrobiologia 571: 341-353. https://doi.org/10.1007/s10750-006-0259-0
  6. Brendonck, L. and L. De Meester. 2003. Egg banks in freshwater zooplankton: evolutionary and ecological archives in sediment. Hydrobiologia 491: 65-84. https://doi.org/10.1023/A:1024454905119
  7. Brucet, S., D. Boix, R. Lopez-Flores, A. Badosa, R. Moreno-Amich and X.D. Quintana. 2005. Zooplankton structure and dynamics in permanent and temporary Mediterranean salt marshes: taxon-based and size-based approaches. Archiv fur Hydrobiologie 162: 535-555. https://doi.org/10.1127/0003-9136/2005/0162-0535
  8. Burks, R.L., E. Jeppesen and D.M. Lodge. 2001. Pelagic prey and benthic predators: impact of odonate predation on Daphnia. The North American Benthological Society 20: 615-628. https://doi.org/10.2307/1468092
  9. Caramujo, M.J. and M.J. Boavida. 2000. Induction and costs of tail spine elongation in Daphnia hyalina x galeata: reduction of susceptibility to copepod predation. Freshwater Biology 45: 413-423. https://doi.org/10.1046/j.1365-2427.2000.00642.x
  10. Dodson, S. and D. Frey. 1991. Cladocera and other Branchiopoda. p. 723-786. In: Ecology and Classification of North American Freshwater Invertebrates (Thorp, J.H. and A.P. Covich, eds.). Academic Press, San Diego.
  11. Dodson, S.I. 1974. Adaptive change in plankton morphology in response to size-selective predation - new hypothesis of cyclomorphosis. Limnology and Oceanography 19: 721-729. https://doi.org/10.4319/lo.1974.19.5.0721
  12. Dumont, H.J. and S.V. Negrea. 2002. Introduction to the class Branchiopoda. Backhuys Publishers, Leiden.
  13. Elendt, B.P. 1990. Selenium deficiency in Crustacea: an ultrastructural approach to antennal damage in Daphnia magna Straus. Protoplasma 154: 25-33. https://doi.org/10.1007/BF01349532
  14. Fry, L.L., M.S. Mulla and C.W. Adams. 1994. Field introductions and establishment of the tadpole shrimp, Triops longicaudatus (Notostraca, Triopsidae), a biological-control agent of mosquitos. Biological Control 4: 113-124. https://doi.org/10.1006/bcon.1994.1019
  15. Han, M.S., K.K. Kang, M.R. Kim, Y.E. Na, H.R. Kim and M.H. Kim. 2013. Characteristics of benthic invertebrates in organic and conventional paddy field. Korean Journal of Environmental Agriculture 32: 17-23. https://doi.org/10.5338/KJEA.2013.32.1.17
  16. Han, M.S., K.K. Kang, Y.E. Na, H.S. Bang, M.H. Kim, M.P. Jung, J.T. Lee, H.K. Hong and D.U. Yoon. 2010. Aquatic invertebrate in paddy ecosystem of Korea. National Academy of Agricultural Science. Suwon, Korea, 416pp.
  17. Haney, J.F. and D.J. Hall. 1973. A preservation technique for cladoceran. Limnology and Oceanography 17: 331-333.
  18. Kim, M.H., M.S. Han, H.K. Nam, K.K. Kang and M.R. Kim. 2012. Geological distribution of aquatic invertebrates living in paddy fields of South Korea. Korean Journal of Soil Science and Fertilizer 45: 1136-1142. https://doi.org/10.7745/KJSSF.2012.45.6.1136
  19. Kwon, S.J., H.Y. Kwon, Y.C. Jun, J.E. Lee and D.H. Won. 2009. Effect of temperature on hatching rate of Triops longicaudatus (Triopsidae, Notostraca). Korean Journal of Limnology 42: 32-38.
  20. Kwon, S.J., Y.C. Jun, J.H. Park, D.H. Won, E.W. Seo and J.E. Lee. 2010. Distribution and habitat characteristics of Tadpole Shrimp (Crustacea: Notostraca; Triops longicaudatus (LeConte)). Korean Journal of Limnology 43: 142-149.
  21. La, G.H., H.G. Jeong, M.C. Kim, G.J. Joo, K.H. Chang and H.W. Kim. 2009. Response of diapausing eggs hatching to changes in temperature and the presence of fish kairomones. Hydrobiologia 635: 399-402. https://doi.org/10.1007/s10750-009-9913-7
  22. Laforsch, C. and R. Tollrian. 2004. Inducible defenses in multipredator environments: cyclomorphosis in Daphnia cucullata. Ecology 85: 2302-2311. https://doi.org/10.1890/03-0286
  23. Lass, S. and P. Spaak. 2003. Chemically induced anti-predator defences in plankton: a review. Hydrobiologia 491: 221-239. https://doi.org/10.1023/A:1024487804497
  24. Lundkvist, E., J. Landin, M. Jackson and C. Svensson. 2003. Diving beetles (Dytiscidae) as predators of mosquito larvae (Culicidae) in field experiments and in laboratory tests of prey preference. Bulletin of Entomological Research 93: 219-226.
  25. Mikulski, A. and J. Pijanowska. 2010. When and how can Daphnia prepare their offspring for the threat of predation? Hydrobiologia 643: 21-26. https://doi.org/10.1007/s10750-010-0131-0
  26. Petrusek, A., R. Tollrian, K. Schwenk, A. Haas and C. Laforsch. 2009. A "crown of thorns" is an inducible defense that protects Daphnia against an ancient predator. Proceedings of the National Academy of Sciences of the United States of America 106: 2248-2252. https://doi.org/10.1073/pnas.0808075106
  27. Pijanowska, J. and G. Stolpe. 1996. Summer diapauses in Daphnia as a reaction to the presence of fish. Journal of Plankton Research 18: 1407-1412. https://doi.org/10.1093/plankt/18.8.1407
  28. Pont, D. and A. Vaquer. 1986. Influence du phyllopode Triops cancriformis (Bosc.) sur la biocenose des rizieres de Camargue. Acta Oecologica 7: 75-88.
  29. Rabus, M. and C. Laforsch. 2011. Growing large and bulky in the presence of the enemy: Daphnia magna gradually switches the mode of inducible morphological defences. Functional Ecology 25: 1137-1143. https://doi.org/10.1111/j.1365-2435.2011.01840.x
  30. Rabus, M., A. Waterkeyn, N.V. Pottelbergh, L. Brendonck and C. Laforsch. 2012. Interclonal variation, effectiveness and long-term implications of Triops-induced morphological defences in Daphnia magna Strauss. Journal of Plankton Research 34: 152-160. https://doi.org/10.1093/plankt/fbr092
  31. Saito, M., A. Miyata, H. Nagai and T. Yamada. 2005. Seasonal variation of carbon dioxide exchange in rice paddy field in Japan. Agricultural and Forest Meteorology 135: 93-109. https://doi.org/10.1016/j.agrformet.2005.10.007
  32. Sakamoto, M., T. Nagata, J.Y. Ha, S. Kimijima and K.H. Chang. 2015. Inducible defenses as factor determining trophic pathways in a food web. Hydrobiologia 743: 15-25. https://doi.org/10.1007/s10750-014-1999-x
  33. Scott, S.R. and A.A. Grigarick. 1979. Laboratory studies of factors affecting egg hatch of Triops longicaudatus (Leconte) (Notostraca : Triopsidae). Hydrobiologia 63: 145-152. https://doi.org/10.1007/BF00030077
  34. Shapiro, J. 1980. The importance of trophic-level interactions to the abundance and species composition of algae in lakes. p. 105-116. In: Hypertrophic Ecosystems (Barica, J. and L.R. Mur, eds.). Dr Junk, Netherlands.
  35. Stibor, H. and W. Lampert. 2000. Components of additive variance in life-history traits of Daphnia hyalina: seasonal differences in the response to predator signals. Oikos 88: 129-138. https://doi.org/10.1034/j.1600-0706.2000.880115.x
  36. Tollrian, R. and C.D. Harvell. 1999. The ecology and evolution of inducible defenses. Princeton University Press, 383pp.
  37. Vandekerkhove, J., S. Declerck, L. Brendonck, J.M. Conde-Porcuna, E. Jeppesen and L. De Meester. 2005. Hatching of cladoceran resting eggs: temperature and photoperiod. Freshwater Biology 50: 96-104. https://doi.org/10.1111/j.1365-2427.2004.01312.x
  38. Von Elert, E. and G. Pohnert. 2000. Predator specificity of kairomones in diel vertical migration of Daphnia: a chemical approach. Oikos 88: 119-128. https://doi.org/10.1034/j.1600-0706.2000.880114.x
  39. Walton, W.E. 2001. Effects of Triops newberryi (Notostraca: Triopsidae) on aquatic insect communities in ponds in the Colorado Desert of Southern California. Israel Journal of Zoology 47: 491-511. https://doi.org/10.1560/MLK8-HEFX-PKUL-LF5Q