우수리땃쥐 Crocidura lasiura의 치아 마모에 의한 연령결정과 번식의 계절적 변이의 조직학적 분석

Age Determination by Tooth Wear and Histological Analysis of Seasonal Variation of Breeding in the Big White-Toothed Shrew, Crocidura lasiura

  • 정순정 (조선대학교 치과대학 구강조직발생학교실) ;
  • 윤명희 (경성대학교 자연과학대학 자연과학부) ;
  • 최정미 (부산정보대학 치위생학과) ;
  • 김현대 (동부산대학교 치위생학과) ;
  • 임도선 (을지대학교 치위생학과) ;
  • 박진주 (조선대학교 치과대학 구강조직발생학교실) ;
  • 최백동 (조선대학교 치과대학 구강조직발생학교실) ;
  • 정문진 (조선대학교 치과대학 구강조직발생학교실)
  • Jeong, Soon-Jeong (Department of Oral Histology & Embryology, School of Dentistry, Chosun University) ;
  • Yoon, Myung-Hee (Division of Natural Science, College of Science, Kyungsung University) ;
  • Choi, Jung-Mi (Department of Dental Hygiene, Busan College of Information Technology) ;
  • Kim, Hyun-Dae (Department of Dental Hygiene, Dong-Pusan College University) ;
  • Lim, Do-Seon (Department of Dental Hygiene, Eulji University) ;
  • Park, Jin-Ju (Department of Oral Histology & Embryology, School of Dentistry, Chosun University) ;
  • Choi, Baik-Dong (Department of Oral Histology & Embryology, School of Dentistry, Chosun University) ;
  • Jeong, Moon-Jin (Department of Oral Histology & Embryology, School of Dentistry, Chosun University)
  • 투고 : 2010.02.28
  • 심사 : 2010.03.23
  • 발행 : 2010.03.31

초록

포획된 야생의 우수리땃쥐 Crocidura lasiura는 구치의 마모와 높이를 이용하여 3개의 연령군으로 분류하였고 번식과 생식기관의 계절적 변이를 조사하였다. 유수들은 구치에서 마모를 가지지 않았고 세 번째 구치 높이가 첫 번째와 두 번째 구치보다 낮았고 비번식상태만을 가졌다. 아성수들은 약간의 마모를 가졌고 세 번째 구치가 첫 번째와 두 번째 구치 높이에 도달했고 성수들은 구치에 깊은 마모를 가졌으며 아성수와 성수는 계절에 따라 번식 혹은 비번식상태를 가졌다. 조직학적 관찰을 근거로 아성수와 성수 수컷의 번식상태는 2월 초에서 10월 초까지 유지되었고 4월에 가장 높은 번식활동을 보였으며 암컷의 번식 상태는 3월 말에서 10월까지 유지되어, 수컷이 암컷보다 빨리 성적 성숙에 이르는 것으로 밝혀졌다. 반면 번식상태는 비번식기 동안 중단되며 이것은 식량자원인 토양 무척추동물의 부족때문이라 생각된다. 번식기의 아성수와 성수들은 많은 생식세포들로 채워진 확장된 세정관을 가지는 큰 정소와 많은 정자들을 가진 팽창된 부정소 미부를 가졌고 10.0 g 이상의 몸무게와 0.03 g 이상의 정소와 부정소 무게를 가졌다. 번식기의 암컷들은 4~6개의 새끼를 가진 임신상태이거나 난소에 성숙난포들과 황체를 가졌고 9.6 g 이상의 몸무게를 가졌다.

Captured wild specimens of the big white-toothed shrew, Crocidura lasiura were classified into three age classes by tooth wear and height of molars, and seasonal variations of breeding and reproductive organs were examined. Juveniles had not tooth wear in molars and height of the third molars were lower than the first and second molars, and had only non-breeding condition. Young adults had little tooth wear and the third molars reached to the first and second molars, and old adults had heavy tooth wear in molars, young adults and old adults had breeding or non-breeding condition according to the season. On the basis of histological examination, seasonal variations of breeding were confirmed that breeding condition of young and old adult males were continued from early February to early October although the breeding activity was the highest in April, that of females were continued from the end of March to October, males reached sexual maturity earlier than females. Whereas the breeding condition seems to cease for non-breeding season because of the deficiency of food resources, soil invertebrates. Young and old adult males of the breeding season had large testes with enlarged seminiferous tubules that were filled with numerous germ cells, and expanded caudal epididymides with a vast number of spermatozoa, and were more than 10.0 g in the body weight and 0.03 g in the testis and epididymis weight. The females of the breeding season were pregnant condition with 4~6 litters or had the Graafian follicles and the corpus lutea in the ovary, and were more than 9.6 g in the body weight.

키워드

참고문헌

  1. Andrews SM, Johnson MS, Cook JA: Cadmium in small mammals from grassland established on metalliferous mine waste. Environ Poll 33 : 153-162, 1984. https://doi.org/10.1016/0143-1471(84)90175-2
  2. Baird DD, Timm RM, Nordquist GE: Reproduction in the Arctic shrew, Sorex arcticus. J Mammal 64 : 298-301, 1983. https://doi.org/10.2307/1380560
  3. Bishop IR, Delany MJ: The ecological distribution of small mammals in the Channel Islands. Mammlia 27 : 99-100, 1963. https://doi.org/10.1515/mamm.1963.27.1.99
  4. Braham HW, Neal CM: The effects of DDT on energetics of the short-tailed shrew, Blarina brevicauda. Bull Environ Contam Tox 12 : 32-37, 1974. https://doi.org/10.1007/BF01713023
  5. Buckner CH: The common shrew (Sorex araneus) as a predator of the winter moth (Operophtera brumata) near Oxford, England. Can Entomol 101 : 370-374, 1969. https://doi.org/10.4039/Ent101370-4
  6. Churchfield S: Population dynamics and the seasonal fluctuations in numbers of the common shrew in Britain. Acta Theriol 25 : 415-424, 1980.
  7. Churchfield S: Water and fat contents of British shrews and their role in the seasonal changes in body weight. J Zool Lond 194 : 165-173, 1981.
  8. Churchfield S: The natural history of shrews. A & C black Ltd, London, pp. 1-11, 24-37, 131-138, 1990.
  9. Corbet GB: The mammals of the palaearctic region: a taxonomic review, British Museum (Nat Hist), Cornell Univ Press, London. pp. 18-30, 1978.
  10. Diamond JB, Sherburne JA: Persistence of DDT in wild populations of small mammals. Nature 221 : 486-487, 1969. https://doi.org/10.1038/221486a0
  11. Genoud M, Vogel P: Energy requirements during reproductioin and reproductive effort in shrews (Soricidae). J Zool Lond 220 : 41-60, 1990. https://doi.org/10.1111/j.1469-7998.1990.tb04293.x
  12. Godfrey GK: The breeding season of the lesser white-toothed shrew (Crocidura suaveolens Pallas, 1811) in Jersey. Bull Soc Jersiaise 22 : 195-196, 1978.
  13. Holling CS: The components of predation as revealed by a study of the small mammal predation of european sawfly. Can Entomol 91 : 293-332, 1959. https://doi.org/10.4039/Ent91293-5
  14. Inoue T: A new method for sexing young of the big-clawed shrew, Sorex unguiculatus (Dobson). J Mamm Soc Japan 13 : 143-145, 1988a.
  15. Inoue T: Territory establishment of young bio-clawed shrew, Sorex unguiculatus (Dobson) (Insectivora, Soricidae). Res Popul Ecol 30 : 83-93, 1988b. https://doi.org/10.1007/BF02512604
  16. Inoue T: Sex difference in spatial distribution of the big-clawed shrew Sorex unguiculatus. Acta Theriol 36 : 229-237, 1991.
  17. Jeong SJ, Yoon MH: Spermatogenesis in three Korean shrews and notes on their phylogenetic significance. Korean Journal of Life Science 11 : 218-229, 2001.
  18. Jeong SJ, Lim DS, Park JC, Kim HJ, Jeong JO, Choi BD, Yoon MH, Jeong MJ: Ultrastructure of the submandibular gland in the big white-toothed shrew, Crocidura lasiura. Korean J Electron Microscopy 35 : 57-64, 2005a.
  19. Jeong SJ, Jeong MJ, Lim DS, Kim DK, Kook JK, Kim HJ, Yoon MH, Park JC: Ultrastructure of the submandibular gland in the lesser white-toothed shrew, Crocidura suaveolens. Korean J Electron Microscopy 35 : 65-72, 2005b.
  20. Jeong SJ, Jeong MJ: Comparative ultrastructure of the acinar cell and secretory granules of the parotid salivary gland in the lesser white-toothed shrew, Crocidura suaveolens and the big whitetoothed shrew, C. lasiura. Korean J Electron Microscopy 35 : 281-287, 2005c.
  21. Jeong SJ, Park JC, Kim HJ, Bae CS, Yoon MH, Lim DS, Jeong MJ: Comparative fine structure of the epididymal spermatozoa from three Korean shrews with considerations on their phylogenetic relationships. Biocell 30 : 279-286, 2006.
  22. Jones JK Jr, Johnson DH: Review of the Insectivores of Korea. Univ Kansas Publ Mus Nat Hist 9 : 549-578, 1960.
  23. Kress A: Ultrastructural studies on oogenesis in the shrew (Crocidura russula) : I. The prenatural follicle. J Morphol 179 : 59-71, 1984. https://doi.org/10.1002/jmor.1051790107
  24. Koh HS: A study on age variation and secondary sexual dimorphism in morphometric characters of Korean rodents: I. An analysis on striped field mice, Apodemus agrarius coreae Thomas, from Cheongju. Korean J Zool 26 : 125-134, 1983.
  25. Mock OB: The least shrew (Cryptotis parva) as a laboratory animal. Laboratory Animal Science 32 : 177-179, 1982.
  26. Pernetta JC: Population ecology of British shrew in grassland. Acta Theriol 22 : 279-296, 1977.
  27. Pucek Z: Seasonal maturation and variability of the reproductive system in young shrew (Sorex L.) in the first calender year of life. Acta Theriol 3 : 269-296, 1960.
  28. Pucek Z: Seasonal and age changes in the weight of internal organs of shrews. Acta Theriol 10 : 369-438, 1965. https://doi.org/10.4098/AT.arch.65-31
  29. Robert RD, Johnson MS, Hutton M: Lead contamination of small mammals from metalliferous mines. Environ Poll 15 : 61-68, 1978. https://doi.org/10.1016/0013-9327(78)90061-7
  30. Rood JP: Observations on population structure, reproduction and molt of the Sicilly shrew. J Mammal 46 : 426-433, 1965. https://doi.org/10.2307/1377629
  31. Tsuchiya K: The chromosomes of Insectivora. In: Oda S, Kitoh J, Ota K, Isomura G, ed, Suncus murinus-Biology of the aboratory shrew, pp. 51-67, Japan Sci Soc Press, Tokyo, 1985.
  32. Won PH: Illustrated encyclopedia and fauna and flora of Korea. Vol. 7, Ministry of education, Korea, pp. 259-283, 1967.
  33. Yoshino H, Abe H: Comparative study on the foraging habits on two species of Soricine shrews. Acta Theriol 29 : 35-43, 1984.