研究生: |
連志台 Lien Chih-Tai |
---|---|
論文名稱: |
小族群台北赤蛙(Rana taipehehsis)的族群動態與年齡結構之探討 The investigation on population dynamics and demography in two small populations of Taipei grass frog (Rana taipehensis) |
指導教授: |
呂光洋
Lue, Kuang-Yang |
學位類別: |
碩士 Master |
系所名稱: |
生命科學系 Department of Life Science |
論文出版年: | 2005 |
畢業學年度: | 93 |
語文別: | 中文 |
論文頁數: | 40 |
中文關鍵詞: | 台北赤蛙 、族群動態 、年齡結構 |
英文關鍵詞: | Rana taipehensis, population dynamics, demography, VORTEX |
論文種類: | 學術論文 |
相關次數: | 點閱:181 下載:13 |
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台北赤蛙(Rana taipehensis van Denburgh, 1909)是一種中小型的蛙類,在台灣的分佈地點目前僅剩下三芝、楊梅、官田及內埔,且族群量都很少。本研究於2003 ~ 2004年,針對三芝、楊梅和內埔地區的族群進行野外調查及年齡結構的分析。
由標記-再捕捉的資料得知:三芝和楊梅地區的台北赤蛙生殖族群性比都偏離1:1,且三芝族群的性比(16.13:1)約是楊梅(6.97:1)的2倍。三芝地區的族群在2003及2004年的推估數量分別為:347、203隻;楊梅地區則為:544、226隻。楊梅地區台北赤蛙在兩次調查間的存活率,依雄、雌蛙不同分別隨著時間而變動;當次調查的遭遇率則依雄、雌蛙不同分別隨著累積降雨量而變動。兩者均是雄蛙比雌蛙高。
藉由趾骨鑑齡得知:台北赤蛙不論雄雌最長壽命均是4歲,但雌蛙(2.58 ±0.09歲)顯著較雄蛙(2.30 ± 0.03歲)大。推測雄蛙在1歲時即可達性成熟並加入生殖族群,雌蛙在2歲時才達性成熟。分別建立2003、2004年的年齡結構後,可推算出跨年的存活率。三芝地區2 --> 3 歲台北赤蛙的存活率:雄蛙 — 0.33;雌蛙 — 0.22。3 -->4歲的存活率:雄蛙 — 0.02;雌蛙 — 0。楊梅地區2 --> 3歲台北赤蛙的存活率:雄蛙 — 0.23;雌蛙 — 0.68。3 --> 4歲的存活率:雄蛙 — 0.06;雌蛙 — 0.12。經Multiple Linear Regression分析的結果,台北赤蛙的吻肛長因年齡、性別、年份及地點而有顯著的不同。
利用VORTEX模擬台北赤蛙的滅絕機率:當雌蛙每年的平均子代數為34隻幼蛙時,楊梅地區的族群到未來第100年時預測的滅絕機率為0;而三芝地區的族群約在未來第26年就完全滅絕了。如將三芝地區的雌蛙數量比例提高約1倍,就可使族群在未來第100年時仍有64%的存活機率,可見適當的性比對台北赤蛙族群的存續是非常重要的。而當雌蛙每年的平均子代數大幅下降時,對族群的存續也有很大的影響。
Abstract
Taipei grass frog (Rana taipehensis van Denburgh, 1909) is a small to median size frog. In Taiwan, the distribution of Taipei grass frog is fragmented in Sanchih, Yangmei, Kuantien, and Neipu. The population size of each study site is very small. From 2003 to 2004, we investigated the population dynamics of Taipei grass frog in Sanchih and Yangmei. After obtaining frog’s age with skeletochronology, we constructed the population age structures of each population.
The sex ratio of reproductive populations in Sanchih and Yangmei both are skewed to males. The ratio for male to female frogs from Sanchih (16.13:1) is almost as twice as the one in Yangmei (6.97:1). Estimated population size with Schnabel method in Sanchih, we got 347 frogs in 2003, and 203 in 2004. Yangmei population was 544 in 2003 and 226 in 2004. In Yangmei, the survival probability changed with time and males have higher survival probability. The encounter probability changed with cumulative precipitation before each surveys and males also have higher encounter probability.
Both in males and females, the oldest frog is 4 years old with skeletochronology. The age of female frog (2.58 ± 0.09LAGs) is significantly older than male (2.30 ± 0.03LAGs). Based on the age structure, males reached to sexual mature and join to the breeding population within 1 year while females in 2 years. The survival rates between age 2 to 3 in Sanchih are: male - 0.33, female - 0.22. The survival rates between age 3 to 4 are: male - 0.02, female - 0. In Yangmei, survival rates are male - 0.23, female - 0.68 between age 2 - 3 and male -0.06, female - 0.12 between age 3 - 4. With Multiple Linear Regression analysis, the result indicated that SVL is significantly different by age, sex, year, and place.
With VORTEX, we simulated the extinction probability of Yangmei population in the 100th year starting from now is 0, when the offspring of a female reproduced is 34.
While in Sanchih will extinct in the 26th year. By doubling the female percentage, the population in Sanchih will have 64% survival probability in the 100th year starting from now. This indicates that sex ratio plays a major role in the persistence of Taipei grass frog. Mean offspring of a female reproduced may also have serious effect, when it dropped sharply.
參考文獻
呂光洋、陳添喜、高善、孫承矩、朱哲民、蔡添順、何一先、鄭正寬,1996。台灣野生動物資源調查—兩棲類動物資源調查手冊。行政院農業委員會。台北。
呂光洋、杜銘章、向高世,1999。臺灣兩棲爬行動物圖鑑。中華民國自然生態保育協會、大自然雜誌社。台北。
周文豪,1994。台北赤蛙的分布及其蝌蚪、鳴聲與保育。自然保育季刊8: 33-39
林曜松、梁世雄,1996。台灣野生動物資源調查—淡水魚資源調查手冊。行政院農業委員會。台北。
林中一,2001。台北縣雙溪河流域褐樹蛙(Buergeria robusta)之生殖生態與族群分布。國立台灣大學動物所碩士論文。
卓瓊玫,2002。霧社地區拉都希氏赤蛙(Rana latouchii)的族群生態研究。台灣師範大學生物所碩士論文。
陳賜隆,1992。翡翠樹蛙(Rhacophorus smaragdinus)生殖行為及生態學之研究。國立台灣師範大學生物所碩士論文。
溫華霞,2001。太魯閣國家公園布洛灣地區莫氏樹蛙(Rhacophorus moltrechti)生殖生態學研究。國立東華大學自然資源管理研究所碩士論文。
楊懿如,1987。台北樹蛙生殖行為之研究。國立台灣大學動物所碩士論文。
楊懿如,2002。賞蛙圖鑑-台灣蛙類野外觀察指南。中華民國自然與生態攝影學會。台北。
蔡雅芬,2002a。古氏赤蛙 (Rana kuhlii) 體型性別二型性之研究。私立東海大學生物所碩士論文。
蔡雅芬,2002b。由骨骼鑑齡法判定兩棲類之年齡。第三次野生動物研究與調查方法研討會。
Alcobendas, M., and J. Castanet, 2000. Bone growth plasticity among populations of Salamandra salamandra: interactions between internal and external factors. Herpetologica 56(1): 14-26
Alexander, M. A., and J. K. Eischeid, 2001. Climate variability in regions of amphibian declines. Conservation Biology 15(4): 930-942
Brook, B. W., J. J. O’Grady, A. P. Chapman, M. A. Burgman, H. R. Akakaya, and R. Frankham, 2000a. Predictive accuracy of population viability analysis in conservation biology. Nature 404: 385-387
Brook, B. W., M. A. Burgman, and R. Frankham, 2000b. Differences and congruencies between PVA packages: the importance of sex ratio for predictions of extinction risk. Conservation Ecology 4(1): 6
Chaloupka, M. Y., and C. J. Limpus, 2002. Survival probability estimates for the endangered loggerhead sea turtle resident in southern Great Barrier Reef waters. Marine Biology 140: 267-277
Eggert, C., and R. Guytant, 1999. Age structure of a spadefoot toad Pelobates fuscus (Pelobatidae) population. Copeia 4: 1127-1130
Ento, K., and M. Matsui, 2002. Estimation of age structure by skeletochronology of a population of Hynobius nebulosus in a breeding season (Amphibia, Urodela). Zoological Science 19: 241-247
Esteban, M., M. Garcia-Paris, and J. Castanet, 1996. Use of bone histology in estimating the age of frogs (Rana perezi) from a warm temperate climate area. Canadian Journal of Zoology 74: 1914-1921
Esteban, M., J. Castanet, and b. Sanchiz, 1998. Inferring age and growth from remains of fossil and predated recent anurans: a test case using skeletochronology. Canadian Journal of Zoology 76: 1689-1695
Esteban, M., M. Garcia-Paris, D. Buckley, and J. Castanet, 1999. Bone growth and age in Rana saharica, a water frog living in a desert environment. Annales Zoologici Fennici 36: 53-62
Esteban, M., and B. Sanchiz, 2002. Differential growth and longevity in low and high altitude Rana iberica (Anura, Ranidae). Herpetol. J. 10: 19-26
Esteban, M., M. J. Snchez-Herriz, L. J. Barbadillo, and J. Castanet, 2004. Age structure and growth in an isolated population of Pelodytes punctatus in northern Spain. Journal of Natural History 38(21): 2789-2801
Freda, J., and W. A. Dunson, 1986. Effects of low pH and other chemical variables on the local distribution of amphibians. Copeia 1986(2): 454-466
Freda, J., W. J. Sadinski, and W. A. Dunson, 1991. Long term monitoring of amphibian populations with respect to the effects of acidic deposition. Water, Air, and Soil Pollution 55: 445-462
Gosner, K. L., and I. H. Black, 1957. The effects of acidity on the development and hatching of New Jersey frogs. Ecology 38(2): 256-262
Grafe, T. U., S. K. Kaminsky, J. H. Bitz, H. Lssow, and K. E. Linsenmair, 2004. Demographic dynamics of the afro-tropical pig-nosed frog, Hemisus marmoratus: effects of climate and predation on survival and recruitment. Oecologia 141: 40-46
Guarino, F. M., F. Andreone, and F. Angelini, 1998. Growth and longevity by skeletochronological analysis in Mantidactylus microtympanum, a rain-forest anuran from southern Madagascar. Copeia 1: 194-198
Guarino, F. M., S. Lunardi, M. Carlomagno, and S. Mazzotti, 2003. A skeletochronological study of growth, longevity, and age at sexual maturity in a population of Rana latastei (Amphibia, Anura). J. Biosce. 28(6): 775-782
Jennings, M., R. Beiswinger, S. Corn, M. Parker, A. Pessier, B. Spencer, and P.S. Miller (eds.), 2001. Population and habitat viability assessment for the Wyoming toad (Bufo baxteri). Final Workshop Report. Apple Valley, MN: IUCN/SSC Conservation Breeding Specialist Group.
Kumbar, S. M., and K. Pancharatna, 2001a. Occurrence of growth marks in the cross section of phalanges and long bones of limbs in tropical anurans. Herpetological Review 32(3): 165-167
Kumbar, S. M., and K. Pancharatna, 2001b. Determination of age, longevity and age at reproduction of the frog Microhyla ornata by skeletochronology. J. Biosci. 26(2): 265-270
Kumbar, S. M., and K. Pancharatna, 2004. Annual formation of growth marks in a tropical amphibian. Herpetological Review 35(1): 35-37
Lima, V., J. W. Arntzen, and N. M. Ferrand, 2000. Age structure and growth pattern in two populations of the golden-striped salamander Chioglossa lusitanica (Caudata, Salamandridae). Amphibia-Reptilia 22: 55-68
Lin, Y.-L., and P.-C. L. Hou, 2002. Applicability of skeletochronology to the anurans from a subtropical rainforest of southern Taiwan. Acta Zoologica Taiwanica 13(1): 21-30
Lindenmayer, D. B., M. A. Burgman, H. R. Akakaya, R. C. Lacy, and H. P. Possingham, 1995. A review of the generic computer programs ALEX, RAMAS/space and VORTEX for modelling the viability of wildlife metapopulations. Ecological Modelling 82: 161-174
Lindenmayer, D. B., and R. C. Lacy, 1995. A simulation study of the impacts of population subdivision on the mountain brushtail possum Trichosurus caninus Ogilby (Phalangeridae: Marsupialia) in south-eastern Australia. I. Demographic stability and population persistence. Biological Conservation 73: 119-129
Lindenmayer, D. B., and R. C. Lacy, 2002. Small mammals, habitat patches and PVA models: a field test of model predictive ability. Biological Conservation 103: 247-265
Lindenmayer, D. B., H. P. Possingham, R. C. Lacy, M. A. McCarthy, and M. L. Pope, 2003. How accurate are population models? Lessons from landscape-scale tests in a fragmented system. Ecology Letters 6: 41-47
Marnell, F., 1998. A skeletochronological investigation of the population biology of smooth newts Triturus vulgaris L. at a pond in Dublin, Ireland. Biology and Environment: Proceedings of the Royal Irish Academy 98B(1): 31-36
Marquez, R., M. Esteban, and J. Castanet, 1997. Size dimorphism and age in midwife toads Alytes obstetricans and A. cisternasii. Journal of Herpetology 31(1): 52-59
Marunouchi, J., T. Kusano, and H. Ueda, 2002. Fluctuation in abundance and age structure of a breeding population of the Japanese brown frog, Rana japonica Gnther (Amphibia, Anura). Zoological Science 19: 343-350
May, R. M., 2004. Ethics and amphibians. Nature 431: 403
McCarthy, M. A., and K. M. Parris, 2004. Clarifying the effect of toe clipping on frogs with Bayesian statistics. Journal of Applied Ecology 41: 780-786
Monnet, J.-M., and M. I. Cherry, 2002. Sexual size dimorphism in anurans. Proc. R. Soc. Lond. B 269: 2301-2307
Morrison, C., J.-M. Hero, J. Browning, 2004. Altitudinal variation in the age at maturity, longevity, and reproductive lifespan of anurans in subtropical Queensland. Herpetologica 60(1): 34-44
Pasanen, S., M. Laitinen, and T. Alhonen, 1998. Effects of pH on the wintering of the common frog (Rana temporaria L.). Ann. Zool. Fennici 35: 29-36
Pistorius, P. A., M. N. Bester, S. P. Kirkman, and F. E. Taylor, 2001. Temporal changes in fecundity and age at sexual maturity of southern elephant seals at Marion Island. Polar Biol. 24: 343-348
Pough, F. H., and R. E. Wilson, 1977. Acid precipitation and reproductive success of Ambystoma salamanders. Water, Air, and Soil Pollution 7: 307-316
Schuble, C. S., 2004. Variation in body size and sexual dimorphism across geographical and environmental space in the frogs Limnodynastes tasmaniensis and L. peronii. Biological Journal of the Linnean Society 82(1): 39-56
Sommer, S., A. T. Volahy, and U. S. Seal, 2002. A population and habitat viability assessment for the highly endangered giant jumping rat (Hypogeomys antimena), the largest extant endemic rodent of Madagascar. Animal Conservation 5: 263-273
Stuart, S. N., J. S. Chanson, N. A. Cox, B. E. Young, A. S. L. Rodrigues, D. L. Fischman, and R. W. Waller, 2004. Status and trends of amphibian declines and extinctions worldwide. Science 306: 1783-1786
Tsiora, A., and P. Kyriakopoulou-Sklavounou, 2002. A skeletochronological study of age and growth in relation to adult size in the water frog Rana epeirotica. Zoology 105(1): 55-60
Wilkinson, D. M., and H. J. O’regan, 2003. Modelling differential extinctions to understand big cat distribution on Indonesian islands. Global Ecology and Biogeography 12: 519-524
Zug, G. R., L. J. Vitt, and J. P. Caldwell, 2001. Herpetology—an introductory biology of amphibians and reptiles, 2nd. Academic press. San Diego.