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한국에서 이매패류 5종의 이성생식세포 발현

Intersexuality of Five Bivalves Species in Korea

초록

본 연구에서는 한국 연안의 생태학적 건강도를 조사하는 과정에서 이매패류 5종 (굴, 지중해담치, 바지락, 대복, 둥글레조개) 에서 발견된 이성생식세포 발현현상을 보고한다. 암컷에서 이성생식세포 발현 현상은 반대 성의 생식세포들이 난자형성소낭 내부와 소낭 사이에서 단독 또는 무리지어 나타나는 형태였다. 이성생식세포 발현 현상이 관찰된 정소에서 난모세포들은 대부분 난황형성전기 또는 난황형성개시기 단계였다. 이들은 단독으로 산재되어 있거나 또는 정자형성소낭의 내부와 소낭 사이에 무리지어 존재하고 있었다. 굴에서 이성생식세포 발현율은 약 10.4% (n = 19/183) 로 수컷 (9.7%, n = 13/134) 보다 암컷 (12.2%, n = 6/49) 에서 높게 나타났다. 지중해담치에서 이성생식세포 발현율은 약 31.7% (n = 19/60) 였으며, 수컷 (25.9%, n = 7/27) 보다 암컷 (36.4%, n = 12/33)에서 높게 나타났다. 바지락 이성생식세포 발현율은 11.2% (n = 11/98) 였는데, 암컷 (7.1%, n = 4/56) 보다 수컷 (16.7%, n = 7/42) 에서 높았다. 대복의 이성생식세포 발현율은 약 28% (n = 30/107) 로 암컷 (24.5%, n = 13/53) 보다 수컷 (31.5%, n = 17/54) 에서 높았다. 둥글레조개에서 이성생식세포 발현율은 약 18.4% (n = 7/38) 였는데, 수컷 (8.3%, n = 2/24) 에 비해 암컷 (35.7%, n = 5/14) 에서 높았다.

keywords
Crassostrea gigas, Mytilus galloprovincialis, Rupiditapes philippinarum, Gomphina veneriformis, Barnea davidi, Intersexuality

Abstract

This research reports the intersexuality of bivalves, such as Crassostrea gigas, Mytilus galloprovincialis, Rupiditapes philippinarum, Gomphina veneriformis and Barnea davidi discovered during the process of investigating the ecological health status of coastal waters of Korea. In intersex ovaries, the opposite germ cells were observed either individually or in groups in the interfollicular space and inside the oogenic follicle. Oocytes in the intersex testis were at the previtellogenic or initial vitellogenic stage. They were either scattered individually or in groups in the interfollicular space and inside the spermatogenic follicle. The intersexuality in C. gigas was 10.4% (n = 19/183), while female (12.2%, n = 6/49) exhibited a higher proportion than male (9.7%, n = 13/134). The intersexuality in M. galloprovincialis was 31.7% (n = 19/60), while female (36.4%, n = 12/33) exhibited a higher proportion than male (25.9%, n = 7/27). The intersexuality in R. philippinarum was 11.2% (n = 11/98), while male (16.7%, n = 7/42) exhibited a higher proportion than female (7.1%, n = 4/56). The intersexuality in G. veneriformis was 28% (n=30/107), while male (31.5%, n=17/54) exhibited a higher proportion than female (24.5%, n=13/53). The intersexuality in B. davidi was 18.4% (n = 7/38), while female (35.7%, n =5 /14) exhibited a higher proportion than male (8.3%, n = 2/24).

keywords
Crassostrea gigas, Mytilus galloprovincialis, Rupiditapes philippinarum, Gomphina veneriformis, Barnea davidi, Intersexuality

참고문헌

1.

Bortone, S.A. and Davis, W.P. (1994) Fish intersexuality as indicator of environmental stress: Monitoring fish reproductive systems can serve to alert humans to potential harm. BioScience, 44: 165-172.

2.

Chesman, B.S. and Langston, W.J. (2006) Intersex in the clam Scrobicularia plana: a sign of endocrine disruption in estuaries? Biology Letters, 2: 420-422.

3.

Gagné, F., Blaise, C., Pellerin, J., Pelletier, E., Douville, M., Gauthier-Clerc, S. and Viglino, L. (2003) Sex alteration in soft-shell clams, Mya arenaria in an intertidal zone of the Saint Lawrence River (Quebec, Canada), Comparative Biochemistry and Physiology Part C, 134: 189-198.

4.

Gauthier-Clerc, S., Pellerin, J., Blaise, C. and Gagné, F. (2002) Delayed gametogenesis of Mya arenaria in the Saguenay fjord (Canada): a consequence of endocrine disruptors? Comparative Biochemistry and Physiology Part C, 131: 457-467.

5.

Gibbs, P.E., Pascoe, P.L. and Burt, G.R. (1988) Sex change in the female dog-whelk, Nucella lapillus induced by tributyltin from antifouling paints. Journal of the Marine Biological Association of the United Kingdom, 68: 715-731.

6.

Guo, X., Hedgecock, D., Hershberger, W.K., Cooper, K., Allen Jr., S.K. Jr. 1998. Genetic determinants of protandric sex in the Pacific oyster, Crassostrea gigas Thunberg. Evolution, 52: 394-402.

7.

Horiguchi, T., Shiraishi, H., Shimizu, M. and Morita, M. (1994) Imposex and organotin compounds in Thais clavigera and T. bronniin in Japan. Journal of the Marine Biological Association of the United Kingdom, 74: 651-669.

8.

Horiguchi, T., Takiguchi, N., Cho, H.S., Kojima, M., Kaya, M., Shiraishi, H., Morita, M., Hirose, H. and Shimizu, M. (2000) Ovo-testis and disturbed reproductive cycle in the giant abalone, Haliotis madaka: possible linkage with organotin contamination in a site of population decline. Marine Environmental Research, 50: 223-229.

9.

Huggett, R.J., Kimerle, R.A., Mehrle, P.M. and Bergman, H.L. (1992) Biomarkers: biochemical, physiological, and histological markers of anthropogenic stress. Lewis Publishers, London, pp. 347.

10.

Iguchi, T. (1998) Environmental endocrine disruptors. Japanese Journal of Clinical Medicine, 56:2953-2962.

11.

Jeon, M.A., Kang, J.C. and Lee, J.S. (2013)Concentration of heavy metal and alteration of reproductive and histological biomarker of Mytilus galloprovincialis in Gamak Bay of the southern coast of Korea. The Korean Journal of Malacology, 29:33-41.

12.

Jeon, M.A., Kim, H., Choi, J.S. and Lee, J.S. (2015)Concentration of trace metals, intersexuality and histological alterations of Ruditapes philippinarum from Gamak Bay in Korea. The Korean Journal of Malacology, 31: 137-142.

13.

Jobling, S., Coey, S., Whitmore, J.G., Kime, D.E., Van Look, K.J.W., McAllister, B.G., Beresford, N., Henshaw, A.C., Brisghty, G., Tyler, C.R. and Sumpter, J.P. (2002) Wild intersex roach, Rutilus rutilus have reduced fertility. Biology of Reproduction, 67: 515-524.

14.

Ju, S.M., Park, J.J. and Lee, J.S. (2009) Induction of intersex and masculinization of the equilateral venus, Gomphina veneriformis (Bivalvia: Veneridae)by zinc. Animal Cells and Systems, 13: 339-344.

15.

Lee, J.S. and Park, J.J. (2007) Risk assessment of nonylphenol using sex ratio, sexual maturation, intersex and lipofuscin accumulation of the equilateral venus, Gomphina veneriformis (Bivalvia:Veneridae). Korean Journal of Fisheries and Aquatic Sciences, 40: 16-23.

16.

Lee, J.S., Lee, Y.G., Kang, S.W., Park, J.S., Lee, D.G., Jeon, M.A. and Ju, S.M. (2010) Intersexuality of Crassostrea gigas and Ruditapes philippinarum in southern coastal waters of Korea. Environmental Health and Toxicology, 25: 287-294.

17.

Lee, J.S., Park, J.S., Shin, Y.K., Lee, Y.G. and Park, J.J. (2013) Sequential hermaphroditism in Manila clam Ruditapes philippinarum (Bivalvia: Veneridae). Invertebrate Reproduction and Development, 57:185-188.

18.

Longnecker, M.P., Rogan, W.J. and Lucier, G. (1997)The human health effects of DDT (dichlorodiphenyl-trichloroethane) and PCBs (polychlorinated biphenyls) and an overview of organochlorines in public health. Annual Reviews Public Health, 18: 211-244.

19.

Matozzo, V. and Marin, M.G. (2005) Can 4-nonylphenol induce vitellogenin-like proteins in the clam, Tapes philippinarum? Environmental Research, 97: 43-49.

20.

Metrio, G.D., Corriero, A., Desantis, S., Zubani, D., Cirillo, F., Deflorio, M., Bridges, C.R., Eicker, J. de la Serna, J.M., Megalofonou, P. and Kime, D.E. (2003) Evidence of a high percentage of intersex in the Mediterranean swordfish, Xiphias gladius L.. Marine Pollution Bulletin, 46: 358-361.

21.

Nilsson, R. (2000) Endocrine modulators in the food chain and environment. Toxicologic Pathology, 28:420-431.

22.

NRC (National Research Council). (1983) Risk assessment in the federal government: managing the process, National Academy Press, Washington DC, pp. 192.

23.

Park, J.J. (2008) Study on the bioindicator of the equilateral venus, Gomphina veneriformis (Bivalvia:Veneridae) chronically exposed to TBT (tributytin chloride). Ph.D. Thesis, Chonnam National University, pp. 222.

24.

Park, J.J., Kim, H., Kang, S.W., An, C.M., Lee, S.H., Gye, M.C. and Lee, J.S. (2012) Sex ratio and sex reversal in two-year-old class of oyster, Crassostrea gigas (Bivalvia: Ostreidae). Development &Reproduction, 16: 385-388.

25.

Quinn, B., Gagné, F., Blaise, C., Costello, M.J., Wilson, J.G. and Mothersill, C. (2006) Evaluation of the lethal the sub-lethal toxicity and potential endocrine distupting effect of nonylphenol on the zebra mussel, Dreissena polymorpha. Comparative Biochemistry and Physiology Part C, 142: 118-127.

26.

Quinn, B., Gagne, F., Costello, M., McKenzie, C., Wilson, J. and Mothersill, C. (2004) The endocrine disrupting effect of municipal effluent on the zebra mussel, Dreissena polymorpha. Aquatic Toxicology, 66:279-292.

27.

Sadovy, Y. and Shapiro, D.Y. (1987) Criteria for the diagnosis of hermaphroditism in fishes. Copeia, 1987:136-156.

28.

Safe, S.H. (2000) Endocrine disruptors and human health: Is there a problem? Environmental Health Perspectives, 108: 487-493.

29.

Shin, Y.K., Park, J.J., Choi, J.S. and Lee, J.S. (2014)Indirect evidence on sex reversal of Sinonovacula comstricta (Bivalvia: Euheterodonta) and Gomphina veneriformis (Bivalvia: Veneridae). Development &Reproduction, 18: 73-78.

30.

Siah, A., Pellerin, J., Amiard, J.-C., Pelletier, E. and Viglino, L. (2003) Delayed gametogenesis and progesterone levels in soft-shell clams, Mya arenaria in relation to in situ contamination to organotins and heavy metals in the St. Lawrence River (Canada). Comparative Biochemistry and Physiology Part C, 135: 145-156.

31.

Tyler, C.R. and Routledge, E.J. (1998) Natural and anthropogenic environmental oestrogens: the scientific basis for risk assessment, oestrogenic effects in fish in English rivers with evidence of their causation. Pure and Applied Chemistry, 70: 1795-1804.

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