Morphometric discrimination of wild from farmed Dybowski’s frog (Rana dybowskii) based on hindlimb length

Rui Xia , Xiao-ming Huang , Shu-hui Yang , Yan-chun Xu , Lu Ying , Thomas D. Dahmer

Journal of Forestry Research ›› 2011, Vol. 22 ›› Issue (2) : 269 -274.

PDF
Journal of Forestry Research ›› 2011, Vol. 22 ›› Issue (2) : 269 -274. DOI: 10.1007/s11676-011-0161-0
Original Paper

Morphometric discrimination of wild from farmed Dybowski’s frog (Rana dybowskii) based on hindlimb length

Author information +
History +
PDF

Abstract

Commercial farming of anuran species that are declining in the wild raises a need to discriminate wild from farmed frogs. We hypothesized wild frogs might have extended hindlimbs due to greater frequency or intensity of jumping relative to farmed frogs, highlighting a morphometric approach to discrimination of wild from farmed frogs using hindlimb length. In the present study, Dybowski’s frog (Rana dybowskii) was used to test this hypothesis. We measured body mass (Mb) and hindlimb length (Lh) of 2-year old farmed frogs and wild frogs aged 2 to 5 years. Dybowski’s frog demonstrated significant dimorphism in Mb and Lh. Mb was significantly greater among farmed 2-year old frogs in both sexes (p=0.000), while only among females was Lh significantly greater for wild frogs (p=0.000). Lh/Mb was used as an index for origin discrimination to eliminate the influence of Mb due to variation of husbandry conditions among farms. Mean Lh/Mb for farmed frogs was significantly lower than for wild frogs (p=0.000) in the 2-year old age class. Discrimination correctly classified 84.4% of farmed and 96.3% of wild male frogs. Among females, 92.9% of farmed frogs and 90.1% wild frogs were correctly classified. The overall correctness of classification was 92.1% and 90.8% for males and females, respectively. However, Lh/Mb revealed variation with age, resulting in reduced discriminative power for frogs ≥3 years old. We introduced a coefficient Ce to adjust the Lh/Mb of frogs ≥3 years to the level equivalent to 2-year frogs. The adjustment achieved 89.5% for overall correctness of origin for wild males and 92.4% for wild females ≥3 years old. These results show that Lh/Mb is an effective index to discriminate wild from farmed Dybowski’s frog. Since the physical demands of jumping are common among anurans, this index is also potentially applicable to other anuran species.

Cite this article

Download citation ▾
Rui Xia, Xiao-ming Huang, Shu-hui Yang, Yan-chun Xu, Lu Ying, Thomas D. Dahmer. Morphometric discrimination of wild from farmed Dybowski’s frog (Rana dybowskii) based on hindlimb length. Journal of Forestry Research, 2011, 22(2): 269-274 DOI:10.1007/s11676-011-0161-0

登录浏览全文

4963

注册一个新账户 忘记密码

References

[1]

Bai Fuxiang, Li Ling, Cai Wei. 2006. Artificial breeding technology of Rana chensinensis. Forest By-Product and Speciality in China, (6): 49–50.(in Chinese)

[2]

Calow L.J., Alexander R.M.. A mechanical analysis of a hind leg of a frog (Rana temporaria). Journal of Physiology, 1973, 171: 293-321.

[3]

Chisholm B.S., Nelson D.E., Schwarcz H.P.. Stable-carbon isotope ratios as a measure of marine versus terrestrial protein in ancient diets. Science, 1982, 216: 1131-1132.

[4]

Edman K.A., Elzinga G., Noble M.I.. Enhancement of mechanical performance by stretch during tetanic contractions of vertebrate skeletal muscle fibers. Journal of Physiology, 1978, 281: 139-155.

[5]

Essner R.L., Suffian D.J., Bishop P.J., Reilly S.M.. Landing in basal frogs: evidence of saltational patterns in the evolution of anuran locomotion. Naturwissenschaften, 2010, 10: 935-939.

[6]

Gary B.G., Richard W.B.. How muscles accommodate movement in different physical environments: aquatic vs. terrestrial locomotion in vertebrates. Comparative Biochemistry and Physiology, 2001, 131: 61-75.

[7]

Hammershøj M., Asferg T., Kristensen N.B.. Comparison of methods to separate wild American mink from fur farm escapees. Mammalian Biology, 2004, 4: 281-286.

[8]

Kelly J.F.. Stable isotopes of carbon and nitrogen in the study of avian and mammalian tropic ecology. Canadian Journal of Zoology, 2000, 78: 1-27.

[9]

Knoff A.J., Macko S.A., Erwin R.M., Brown K.M.. Stable isotope analysis of temporal variation in the diet of pre-fledged laughing gulls. Waterbirds, 2002, 25: 142-148.

[10]

Leisler B.. Die ökologische bedeutung der locomotion mitteleuropäischer Schwirle (Locustella). Egretta, 1977, 117: 397-418.

[11]

Li T., Jiang Lan.. Artificial breeding of Rana chensinensis in the northeast forest. Forest By-Product and Speciality in China, 1987, 2: 19-22.

[12]

Liu Xin, Zhang Wei, Yu Baocheng, Liu Weishi. 2007. Investigation on Rana chensinensis resources in the three northeastern provinces of China. Forest Resources Management, (3): 82–85.

[13]

Lutz G.J., Rome L.C.. Built for jumping: the design of the frog muscular system. Science, 1994, 263: 370-372.

[14]

Mai M.T., Lieber R.L.. A model of semitendinosus muscle sarcomere length, knee and hip joint interaction in the frog hindlimb. Journal of Biomechanics, 1990, 23: 271-279.

[15]

McPhee M.E.. Effects of captivity on response to a novel environment in the old field mouse (Peromyscus polionotus subgriseus). International Journal of Comparative Psychology, 2003, 16: 85-94.

[16]

McPhee M.E.. Generations in captivity increases behavioral variance: Considerations for captive breeding and reintroduction programs. Biological Conservation, 2003, 115: 71-77.

[17]

McPhee M.E.. Morphological change in wild and captive old field mice Peromyscus polionotus subgriseus. Journal of Mammalogy, 2004, 85: 1130-1137.

[18]

Meng D., Yu H., Meng G., Lei Guanglin.. Initial report on semi-artificial breeding of Rana chensinensis. Journal of Liaoning Forestry Science and Technology, 1990, 2: 57-61.

[19]

Olson J.M., Marsh R.L.. Activation patterns and length changes in hindlimb muscles of the bullfrog (Rana catesbeiana) during jumping. Journal of Experimental Biology, 1998, 201: 2763-2777.

[20]

Ostwald R., Okey R., Shannon A., Tinoco J.. Changes in tissue lipids in response to diet. I. fatty acids of subcutaneous, mesenterio and interscapular fat. Journal of Nutrition, 1962, 76: 341-352.

[21]

Peplowski M.M., Marsh R.L.. Work and power output in the hind-limb muscles of Cuban tree frogs Osteopilus septentrionalis during jumping. Journal of Experimental Biology, 1997, 200: 2861-2870.

[22]

Rouvinen K., Kiiskinen T.. Influence of dietary fat source on the body fat composition of mink (Mustela vison) and blue fox (Alopex lagopus). Acta Agriculturae Scandinavica, 1989, 39: 279-288.

[23]

Smith R.J., Hobson K.A., Koopaman H.N., Lavigne D.M.. Distinguishing between populations of fresh- and saltwater harbour seals (Phoca vitulina) using stable-isotope ratios and fatty acid profiles. Canadian Journal of Fisheries and Aquatic Sciences, 1996, 53: 272-279.

[24]

Watanabe M., Kaga M., Matsueda M., Takahashi K.. The effect of sports activity on tibial bone strength in junior high school students. International Journal of Sports and Health Science, 2007, 5: 116-121.

[25]

Xie F., Ye C., Fei L., Jiang J., Zeng X., Masafumi Matsui.. Taxonomical studies on brown frogs (Rana) from northeastern China (Amphibia: Ranidae). Acta Zoo Taxonomica Sinica, 1999, 24: 224-231.

[26]

Yang S.H., Huang X.M., Xia R., Xu Y.C., Dahmer T.D.. Use of femur bone density to segregate wild from farmed Dybowski’s frog (Rana dybowskii). Forensic Science International, 2011, 207: 61-65.

AI Summary AI Mindmap
PDF

131

Accesses

0

Citation

Detail

Sections
Recommended

AI思维导图

/