DOI QR코드

DOI QR Code

Characteristics of External and Cranial Morphological Characters of Asian Lesser White-Toothed Shrew (Crocidura shantungensis)

작은땃쥐 (Crocidura shantungensis)의 외부 형태 및 두개골 형질의 특성

  • Kim, Tae-Wook (Faculty of Science Education, Jeju National University) ;
  • Park, Su-Gon (Faculty of Science Education, Jeju National University) ;
  • Kim, Yoo-Kyung (Faculty of Science Education, Jeju National University) ;
  • Park, Jun-Ho (Faculty of Science Education, Jeju National University) ;
  • Adhikari, Pradeep (Faculty of Science Education, Jeju National University) ;
  • Kim, Ga-Ram (Faculty of Science Education, Jeju National University) ;
  • Park, Seon-Mi (Faculty of Science Education, Jeju National University) ;
  • Lee, Jun-Won (Faculty of Science Education, Jeju National University) ;
  • Han, Sang-Hyun (Educational Science Research Institute, Jeju National University) ;
  • Oh, Hong-Shik (Faculty of Science Education, Jeju National University)
  • 김태욱 (제주대학교 과학교육학부) ;
  • 박수곤 (제주대학교 과학교육학부) ;
  • 김유경 (제주대학교 과학교육학부) ;
  • 박준호 (제주대학교 과학교육학부) ;
  • ;
  • 김가람 (제주대학교 과학교육학부) ;
  • 박선미 (제주대학교 과학교육학부) ;
  • 이준원 (제주대학교 과학교육학부) ;
  • 한상현 (제주대학교 교육과학연구소) ;
  • 오홍식 (제주대학교 과학교육학부)
  • Received : 2015.10.30
  • Accepted : 2015.12.10
  • Published : 2015.12.31

Abstract

This study was conducted to screen the characteristics of external and cranial characters of Crocidura shantungensis collected from Korean Peninsula, Ulleung Island and Jeju Island. There were significant differences in head-body length (HBL), tail length (TL), ear length (EL), and hind foot length (HFL) in males and HBL, TL, and HFL in females among three populations (p<0.05). The HBL and TL in the Jeju Island population were larger (8.0 mm and 4.0 mm in lengths, respectively) than those of the Korean Peninsula population. Based on skull analysis, a total of thirteen traits showed significant differences among the three populations (p<0.05). The condylo-insicive length (CIL), maximum width of brain case (MWB), mandibular length (ML), and mandibular height (MH) in the Jeju Island population were significantly larger than those of Korean Peninsula population (p<0.05). Principle component analysis (PCA) showed that two principle components (PC) identified from the PCA affected on the body size and width of the skull, respectively. Discriminant analysis revealed that these populations could be discriminated through skull traits. These findings concluded that the Jeju Island population was greater in the size than the Korean Peninsula, suggesting that the Jeju Island shrews have successfully adapted to the island environments and they had morphologically differentiated during glacial period after natural immigration into that Island. Thus, this study supports the 'Island Rule', showing that the population is well adapted to the island environments. This may provide important information for biogeographical and ecological studies on insular animals.

본 연구는 한반도, 울릉도, 제주도에서 수집한 작은땃쥐 (Crocidura shantungensis)의 외부형태와 두개골 형질의 특성을 살펴보기 위하여 수행하였다. 외부형태 비교 결과, 수컷은 HBL, TL, EL, HFL 등 조사된 모든 크기 형질에서 (p<0.05), 암컷은 HBL, TL, HFL에서 세 집단 사이의 유의차가 관찰되었다 (p<0.05). 제주도 집단은 HBL이 한반도 집단보다 약 8.0 mm 이상 더 길고, TL은 약 4.0 mm 이상 더 길었다. 두개골 형질에 대한 분석결과, 조사된 16개 형질 가운데 13개 형질에서 작은땃쥐 세 집단 사이의 유의적인 차이가 발견되었다 (p<0.05). 주성분 분석에서 결정된 2가지 주성분들은 두개골의 전반적인 크기와 좌우 너비가 중요하게 작용하였다. 판별 분석결과에서 두개골 형질에 의한 제주도와 한반도-울릉도 집단은 뚜렷하게 구분되었다. 제주도 집단이 한반도 집단에 비해 외부형태와 두개골이 더 크다는 본 연구결과는 C. shantungensis가 제주도로 유입된 이후 빙하기를 거치는 동안 성공적으로 제주도 환경에 적응하면서 형태적으로 분화되었음을 제안하였다. 본 연구결과는 섬 환경에 적응된 집단에서 나타나는 섬 법칙을 지지하고 있으며, 향후 섬 동물의 생물지리학과 생태학 연구에 중요한 역할을 수행할 것이다.

Keywords

References

  1. Abramov AV. 2005. On a taxonomic position of the weasel (Carnivora, Mustela) from the Cheju Island (South Korea). Russ. J. Theriol. 4:109-113.
  2. Bannikova AA, BI Sheftel, VS Lebedev, DY Aleksandrov and M Muehlenberg. 2009. Crocidura shantungensis, a new species for Mongolia and Buryatia. Dokl. Biol. Sci. 424:68-71. https://doi.org/10.1134/S0012496609010207
  3. Chung CH. 2007. Vegetation response to climate change on Jeju Island, South Korea, during the last deglaciation based on pollen record. Geosci. J. 11:147-155. https://doi.org/10.1007/BF02913928
  4. Chung KH and HJ Yang. 1999. A study on the fauna and speciation of the Cheju Island and Ulrung dagelet in Korea. J. Kyonggi Basic Sci. 12:189-200.
  5. Fairbank RG. 1989. A 17,000-year glacio-eustatic sea level record: influence of glacial melting rates on the Younger Dryas event and deep-ocean circulation. Nature 342:637-642. https://doi.org/10.1038/342637a0
  6. Foster JB. 1964. Evolution of mammals on islands. Nature 202:234-235. https://doi.org/10.1038/202234a0
  7. Goodman SM, CP Maminirina, HM Bradman, L Christidis and BR Appleton. 2009. Patterns of morphological and genetic variation in the endemic Malagasy bat Miniopterus gleni (Chiroptera: Miniopteridae), with the description of a new species, M. griffithsi. J. Zoolog. Syst. Evol. Res. 48:75-86.
  8. Han SH, MA Iwasa, SD Ohdachi, HS Oh, H Suzuki, K Tsuchiya and H Abe. 2002. Molecular phylogeny of Crocidura shrews in northeastern Asia: A special reference to specimens in Cheju Island, South Korea. Acta Theriol. 47:369-379. https://doi.org/10.1007/BF03192463
  9. Hernandez-Salinas U, A Ramirez-Bautista, NP Pavon and LFR Pacheco. 2014. Morphometric variation in island and mainland populations of two lizard species from the Pacific coast of Mexico. Rev. Chil. Hist. Nat. 87:21. https://doi.org/10.1186/s40693-014-0021-3
  10. Hutterer R. 2005. Order Soricomorpha, pp. 220-311. In Mammal Species of the World: A Taxonomic and Geographic Reference, Wilson DE and DM Reeder (3rd eds.). The Johns Hopkins University Press, Baltimore.
  11. Ijiri A, L Wang, T Oba, H Kawahata, CY Huang and CY Huang. 2005. Paleoenvironmental changes in the northern area of the East China Sea during the past 42,000 years. Palaeogeogr. Palaeoclimatol. Palaeoecol. 219:239-261. https://doi.org/10.1016/j.palaeo.2004.12.028
  12. Iwasa MA, S Ohdachi, SH Han, HS Oh, H Abe and H Suzuki. 2001. Karyotype and RFLP of the nuclear rDNA of Crocidura sp. on Cheju Island, South Korea (Mammalia, Insectivora). Mammalia 65:451-459. https://doi.org/10.1515/mamm.2001.65.4.451
  13. Jeong SJ, MH Yoon, SH Kim, JH Ham, DS Lim, BD Choi, JJ Park and MJ Jeong. 2010. Age determination by tooth wear and histological analysis of seasonal variation of breeding in the lesser white-toothed shrew, Crocidura suaveolens. Korean J. Microsc. 40:125-132.
  14. Jo YS, TW Kim, BJ Choi and HS Oh. 2012. Current status of terrestrial mammals on Jeju Island. J. Species Res. 1:249-256. https://doi.org/10.12651/JSR.2012.1.2.249
  15. Kim JM and JP Kennett. 1998. Paleoenvironmental changes associated with Holocene marine transgression, Yellow Sea (Hwanghae). Mar. Micropaleontol. 34:71-89. https://doi.org/10.1016/S0377-8398(98)00004-8
  16. Kim TW, SG Park, YK Kim, JH Park, P Adhikari, GR Kim, SM Park, JW Lee, SH Han and HS Oh. 2015. Sexual size differences of morphological and skull traits in the Jeju Island population of lesser white-toothed shrew (Crocidura shantungensis). J. Emb. Trans. (in processing).
  17. Koh HS and BS Yoo. 1992. Variation of mitochondrial DNA in two subspecies of striped field mice, Apodemus agrarius coreae and Apodemus agrarius chejuensis, from Korea. Korean J. Zool. 35:332-338.
  18. Maldonado JE, F Hertel and C Vila. 2004. Discordant patterns of morphological variation in genetically divergent populations of Ornate shrews (Sorex ornatus). J. Mammal. 85:886-896. https://doi.org/10.1644/1545-1542(2004)085<0886:DPOMVI>2.0.CO;2
  19. Martin JGA, M Festa-Bianchet, SD Cote and DT Blumstein. 2013. Detecting between-individual differences in hindfoot length in population of wild mammals. Can. J. Zool. 98:118-123.
  20. Millien V. 2006. Morphological evolution is accelerated among island mammals. PLoS Biol. 4:1863-1868.
  21. Millien V and J Damuth. 2004. Climate change and size evolution in an island rodent species: New perspectives on the island rule. Evolution 58:1353-1360. https://doi.org/10.1111/j.0014-3820.2004.tb01713.x
  22. Motokawa M, LK Lin, M Harada and S Hattori. 2003. Morphometric geographic variation in the Asian lesser white-toothed shrew Crocidura shantungensis (Mammalia, Insectivora) in east Asia. Zool. Sci. 20:789-795. https://doi.org/10.2108/zsj.20.789
  23. Ochocinska D and JRE Taylor. 2003. Bergmann's rule in shrews: geographical variation of body size in Palearctic Sorex species. Biol. J. Linn. Soc. Lon. 78:365-381. https://doi.org/10.1046/j.1095-8312.2003.00150.x
  24. Oh HS, Y Yoshinaga and T Mori. 1998. Reproduction in the wild population of the Korean striped field mouse, Apodemus agrarius chejuensis. J. Fac. Agr. Kyushu U. 42:383-395.
  25. Oh HS, Y Yoshinaga, T Kaneko, H Iida and T Mori, 2003. Taxonomic re-examination of the Apodemus agrarius chejuensis, comparing external and cranial morphological characters among four Asian Apodemus species. J. Fac. Agr. Kyushu U. 47:373-386.
  26. Oh HS, MH Chang and BS Kim. 2007. Current status of mammals in Hallasan National Park. Korean J. Environ. Ecol. 21:235-242.
  27. Ohdachi SD, MA Iwasa, VA Nesterenko, H Abe, R Masuda and W Haberl. 2004. Molecular phylogenetics of Crocidura shrews (Insectivora) in east and central Asia. J. Mammal. 85:396-403. https://doi.org/10.1644/1545-1542(2004)085<0396:MPOCSI>2.0.CO;2
  28. Park YA, BK Khim and S Zhao. 1994. Sea level fluctuation in the Yellow Sea Basin. J. Korean Soc. of Oceano. 29:42-49.
  29. Park YS, WS Lee, JT Kim and HS Oh. 2011. Morphological examination of the Siberian roe deer Capreolus pygargus in South Korea. J. Anim. Vet. Adv. 10:2847-2878.
  30. Smith HF, CE Terhune and CA Lockwood. 2007. Genetic, geographic, and environmental correlates of juman temporal bone varation. Am. J. Phys. Anthropol. 134:312-322. https://doi.org/10.1002/ajpa.20671
  31. Thorpe RS. 1987. Geographic variation: a synthesis of cause, data, pattern and congruence in relation to subspecies, multivariate analysis and phylogenesis. Boll. Zool. 54:3-11. https://doi.org/10.1080/11250008709355549
  32. van Valen L. 1973. A new evolutionary law. Evol. Theor. 1:1-30.
  33. Vega R, G Amori, G Aloise, S Cellini, A Loy and JB Searle. 2010. Genetic and morphological variation in a mediterranean glacial refugium: evidence from Italian pygmy shrews, Sorex minutus (Mammalia: Soricomorpha). Biol. J. Linn. Soc. Lon. 100:774-787. https://doi.org/10.1111/j.1095-8312.2010.01454.x
  34. White TA and JB Searle. 2007. Factors explaining increased body size in common shrews (Sorex araneus) on Scottish islands. J. Biogeogr. 34:356-363. https://doi.org/10.1111/j.1365-2699.2006.01599.x
  35. Wilson LAB. 2013. Geographic variation in the greater Japanese shrew-mole, Urotrichus talpoides: Combining morphological and chromosomal patterns. Mamm. Biol. 78:267-275. https://doi.org/10.1016/j.mambio.2012.09.003
  36. Yoon MH, SH Han, HS Oh and JG Kim. 2004. Mammals of Korea. Dongbang Media, Seoul, pp. 24-27.
  37. Yoon MH, I Kim, HS Oh and CJ Phillips. 2003. Biogeography, Genetic structure, and speciation in the striped field mouse, Apodemus agrarius, in Southern Korea. Korean J. Genetic. 26:15-28.
  38. Zidarova S. 2015. Is there sexual dimorphism in shrew? A case study of six European species of the Family Soricidae. Acta Zool. Bulgar. 67:19-34.