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Author: 林華慶
Hua-Ching Lin
Thesis Title: 赤尾青竹絲之族群生態學研究
Population ecology of chinese tree viper, Trimeresurus stejnegeri stejnegeri
Advisor: 杜銘章
Tu, Ming-Chung
Degree: 博士
Doctor
Department: 生命科學系
Department of Life Science
Thesis Publication Year: 2006
Academic Year: 94
Language: 英文
Number of pages: 91
Keywords (in Chinese): 台灣存活率補取率生長率壽命年齡雌雄體型二型性微棲地選擇溫度休憩地點植被密度獵物可及性
Keywords (in English): snakes, Taiwan, survival, capture probabilities, growth rate, longevity, age, sexual-size dimorphism(SSD), microhabitat selection, temperature, retreat site, vegetation density, prey acailability
Thesis Type: Academic thesis/ dissertation
Reference times: Clicks: 312Downloads: 19
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  • 中文摘要

    生物個體在生殖、成長與棲息地選擇方面的差異是導致它們擁有不同適合度(fitness)的重要原因,同時也是天擇作用於物種或是族群的原動力之一。赤尾青竹絲(Trimeresurus s. stejnegeri)是台灣常見的樹棲性蝮蛇,夜行性,採定點埋伏捕食策略;具有明顯的性別體型二型性(sexual-size dimorphism,SSD),雌蛇體型較大。本論文以赤尾青竹絲為對象,研究其族群生態、生活史特性與微棲地選擇,內容共分為三章。
    第一章與第二章是我藉由對苗栗縣造橋鄉平興村的野外赤尾青竹絲族群,以重複捕取(mark-recapture)的方法獲得長達9年以上的群體研究(demography)資料,據以估算赤尾青竹絲的存活率,並探討此一族群的雄蛇明顯多於雌蛇的原因;此外我也研究赤尾青竹絲的生長,並探討其性別體型二型性的形成原因。第三章則是研究植被遮蔽(vegetation cover)、獵物可及性(prey availability)與環境溫度對於赤尾青竹絲選擇日間停棲地點(diurnal retreat site)的影響性,為了避免野外眾多環境因子交互影響又常難以釐清,此部分研究在戶外網室中進行。
    在第一章中,我從1996年5月至2005年8月期間共計標放577隻赤尾青竹絲,所有的捕取資料共計2095隻次。以Jolly-Seber模式估算的結果,整體族群的平均存活率為0.72;尚未性成熟的個體(immature)其平均存活率為0.62,顯著較性成熟後的成蛇存活率(0.73)為低,但年輕成蛇與年長成蛇的存活率則無顯著差異。族群內雄蛇與雌蛇隻數的平均比值為2.51(雄蛇/雌蛇),而且雄蛇顯著多於雌蛇的現象持續存在於研究中的每個半年期間(以雌蛇的生殖期前、後為區分)。惟在不同的生活史階段,新生幼蛇(newborn)與尚未性成熟的亞成蛇(juvenile),其性別比均未偏離1:1;但在性成熟後,雄性成蛇顯著多於雌性成蛇,而且隨著體長或年齡的增長,雄蛇多於雌蛇的趨勢更加顯著。比較不同性別之存活率,性成熟前,雄蛇與雌蛇之平均存活率並無顯著差異(雄蛇為0.62,雌蛇為0.63);惟性成熟後,雌蛇的平均存活率(0.65)顯著低於雄蛇(0.75),而兩性間的捕取率並無顯著差異(雄蛇為0.65,雌蛇為0.61)。從研究結果推測,雌性赤尾青竹絲在性成熟後,因為較高的生殖成本(cost of reproduction)而導致其存活率較雄蛇低,同時也導致此一族群的雄性成蛇數量顯著多於雌性。
    在第二章中,我分析造橋赤尾青竹絲的生長模式、估測其年齡結構,並比較性別間的差異。性成熟前,赤尾青竹絲的平均吻肛長(SVL)與體重並未有性別間的差異;性成熟後,雌蛇的體重顯著大於雄蛇。不同生活史階段的群體間,新生幼蛇的吻肛長(SVL)與體重並未有性別間的差異;但在亞成蛇階段,雌蛇的吻肛長與體重均顯著大於雄蛇,且此差異性同樣出現於年輕成蛇與年長成蛇階段,顯示赤尾青竹絲的性別體型二型性是從亞成蛇階段開始發生。此外,性成熟前雌蛇的生長速率(0.28 mm/day)明顯高於雄蛇(0.19 mm/day),性成熟後二者則無顯著差異。雌蛇較雄蛇更早性成熟,雄蛇達到性成熟體長所需的平均時間為2.6年,雌蛇僅需1.9年;而年齡結構也有顯著的性別間差異,雌性赤尾青竹絲的平均年齡(4.0)顯著低於雄蛇(5.2),5歲以及5歲以上的雄蛇佔所有雄性個體的36.8 %,而同樣年齡層的雌蛇僅佔11.9 %。赤尾青竹絲的性別體型二型性肇因於雌蛇在性成熟前的快速生長,以及在性成熟之後以與雄蛇相近的速率持續生長;這可能是因為赤尾青竹絲面臨雌性成蛇較低的存活率與較短的壽命,而演化出快速生長與快速生殖以獲得較高生殖成功(reproductive success)的生存策略;而雌、雄蛇間的存活率差異導致年長雌蛇的數量較少,也使得所有雌性成蛇的平均吻肛長並未大於雄性成蛇,致使性別間實際存在的體長二型性未能顯現。
    第三章,我藉由操控植栽排列的疏密程度與距離食物資源遠近,以及記錄環境溫度變化的情況下,研究植被遮蔽、獵物可及性以及溫度對赤尾青竹絲選擇日間停棲地點的影響性。結果發現,溫度是影響赤尾青竹絲選擇日間停棲地點的最重要因子,赤尾青竹絲於日間停棲在植栽上的高度明顯受到環境溫度的影響,當環境溫度較高時,牠們趨向停棲於溫度較低的植被下層。赤尾青竹絲對不同植被遮蔽程度的選擇也同樣受到溫度的影響,當環境溫度高於25C時,赤尾青竹絲趨向停棲於溫度較低的植被較密處;當環境溫度低於25C時,除了完全不選擇去除所有葉片而最為稀疏的植被結構外,赤尾青竹絲對於植被的疏密程度並未有明顯偏好。其日間停棲地點在不同時間與不同季節的變異,應該是為了滿足體溫調節需求所作的調整。

    Abstract

    Reproduction, growth and habitat selection of an organism can make a strong impact on its long-term fitness. Variation in fitness among individuals plays a primary force in natural selection. The Chinese green tree viper (Trimeresurus s. stejnegeri), a nocturnal, arboreal sit-and-wait predator, is one of the most common snakes in Taiwan. This serpent exhibits an obviously female-biased sexual-size dimorphism (SSD). It often retreats into vegetation during daytime and moves to ambush sites at dusk. Furthermore, a pattern of male-biased sex ratio was found in a population of Trimeresurus s. stejnegeri at Tsaochiao in the northern Taiwan. In this dissertation, I used demographic analysis from an over nine-year (1996-2005) mark-recapture data set of the population of Trimeresurus s. stejnegeri at Tasochiao, to explore the causes of observed male-biased sex ratio and female-biased SSD. Additionally, I applied an experimental approach to investigate the role of temperature, prey availability and vegetation density with respect to diurnal retreat site selection of the Chinese green tree vipers in outdoor enclosures.
    In Chapter I, the sex ratio and survivorship of the Chinese green tree viper Trimeresurus s. stejnegeri in Tsaochiao, Taiwan were investigated monthly by mark-recapture method from 1996 to 2005. A total of 577 individuals were captured and 2095 observations were made. They showed significant male-biased sex ratios with an average of 2.51 (male/females) for the half-year reproductive and postpartum periods. The male-biased sex ratio was not observed at the immature (newborn + juvenile) stage but at the adult stage. The average estimates of half-year survival rates and catch probability were 0.72 and 0.65, respectively. The survival rates were lower at the immature stage than adult stage, but they were not significantly different between immature males (mean survival rate, 0.62) and immature females (0.63). In contrast, the survival rate of adult females (0.65) was lower than that of adult males (0.75), but there was no significant difference in average capture probabilities between the two sexes (0.65 for males and 0.61 for female). Costs of reproduction in females, such as physical burden during gestation and emaciated condition after parturition are suggested as the primary causes for lower survivorship of adult females than adult males.
    In Chapter II, using the data of 577 individuals collected from the nine-year mark-recapture study, sexual differences in growth and body sizes were examined for the different life stages of the Chinese green tree viper Trimeresurus s. stejnegeri in Tsaiochio. The results showed that there were no significant sexual differences in SVL and body weight at the newborn stage but the differences were significant at the juvenile stage, young adult stage, and old adult stage. These indicated that the SSD of the Chinese green tree viper occurs at the post-newborn life stages after the first year of life. Growth rates were significantly faster for females (0.28 mm/day) than males (0.19 mm/day) at the immature stage but not at the adult stage. The Chinese green tree viper became reproductive maturity at the ages of 2.6 years for males and 1.9 years for females. Male-biased age distributions were observed for the old adult snakes; the average age of adult males was 5.2 years whereas females was 4.0 years, indicating that the females had lower survivorship and shorter life span than the males at the adult stage. The proximate mechanisms for SSD of the Chinese green tree viper are that females grow faster and larger than males at the immature stage. By doing so, the females reach sexual maturity faster and increase their reproductive fecundity. This may be evolved as a surviving strategy to compensate the lower survivorship and shorter life span at the adult stage of female Chinese green tree vipers.
    In Chapter III, I manipulated vegetation structure, distance to prey source, and monitoring the microhabitat temperature within the test enclosures. The results indicated that the height of daytime perch sites was influenced by ambient temperature. Snakes perched on lower layers of vegetation seeking cooler conditions when ambient enclosure temperature was high. In addition, when the ambient temperature rose above 25C, Trimeresurus s. stejnegeri retreated into denser vegetation, which provided significantly lower temperatures. In contrast, Trimeresurus s. stejnegeri in low temperature environments did not exhibit any preference for vegetation structures in terms of density, except for an apparent avoidance of vegetation with bare branches and no leaves. The distance to prey source did not appear to have any significant influence on the green tree viper’s selection of retreat site, this could be attributed to the fact that these snakes do not only hunt terrestrial preys, but also prey upon arboreal species. This study demonstrated that temperature was the most important factor influencing retreat site selection of Trimeresurus s. stejnegeri. The temporal variations and seasonal differences in the space utilization patterns may have been for the purpose of satisfying their thermoregulation needs.

    Contents 中文摘要 1 Abstract 4 General Introduction 7 Chapter I 11 Male-biased sex ratio and survivorship of the Chinese green tree viper (Trimeresurus s. stejnegeri) in the northern Taiwan Introduction 11 Materials and Methods 14 Results 18 Discussion 21 Figures 28 Tables 30 Chapter II 35 Sexual differences in growth and body size of the Chinese green tree viper Trimeresurus s. stejnegeri in the northern Taiwan Introduction 35 Materials and Methods 37 Results 40 Discussion 45 Figures 53 Tables 58 Chapter III 61 Diurnal Retreat Site Selection by the Arboreal Chinese Green Tree Viper (Trimeresurus s. stejnegeri) as Influenced by Temperature Introduction 61 Materials and Methods 64 Results 70 Discussion 74 Figures 81 Tables 86 Conclusions 87 References 91

    References
    Aldridge, R. D., and W. S. Brown. 1995. Male reproductive-cycle, age at maturity, and cost of reproduction in the timber rattlesnake (Crotalus horridus). J. Herpetol. 29:399-407.
    Andersson, M. 1994. Sexual selection. Princeton University Press, New Jersey.
    Andrews, R. M. 1982. Patterns of growth in reptiles. Pages 273-334 in C. Gans and F. H. Pough, editors. Biology of the Reptilia, Vol. 13. Academic Press, New York.
    Beaupre, S. J. 2002. Modeling time-energy allocation in vipers: individual responses to environmental variation and implication for populations. in G. W. Schuett, M. Hoggren, M. E. Douglas, and H. W. Greene, editors. Biology of the vipers. Eagle Mountain Publishing, Eagle Mountain, UT.
    Blem, C. R., and L. B. Blem. 1995. The eastern cottonmouth (Agkistrodon Piscivorus) at the northern edge of its range. J. Herpetol. 29:391-398.
    Blouin-Demers, G., K. A. Prior, and P. J. Weatherhead. 2002. Comparative demography of black rat snakes (Elaphe obsoleta) in Ontario and Maryland. J. Zool. 256:1-10.
    Blouin-Demers, G., and P. J. Weatherhead. 2002. Habitat-specific behavioural thermoregulation by black rat snakes (Elaphe obsoleta obsoleta). Oikos 97:59-68.
    Bonnet, X., O. Lourdais, R. Shine, and G. Naulleau. 2002. Reproduction in a typical capital breeder: Costs, currencies, and complications in the aspic viper. Ecology 83:2124-2135.
    Bonnet, X., G. Naulleau, R. Shine, and O. Lourdais. 1999. What is the appropriate timescale for measuring costs of reproduction in a 'capital breeder' such as the aspic viper? Evol. Ecol. 13:485-497.
    Bonnet, X., G. Naulleau, R. Shine, and O. Lourdais. 2000. Reproductive versus ecological advantages to larger body size in female snakes, Vipera aspis. Oikos 89:509-518.
    Bonnet, X., G. Naulleau, R. Shine, and O. Lourdais. 2001. Short-term versus long-term effects of food intake on reproductive output in a viviparous snake, Vipera aspis. Oikos 92:297-308.
    Brito, J. C., and R. Rebelo. 2003. Differential growth and mortality affect sexual size dimorphism in Vipera latastei. Copeia 2003:865-871.
    Brodie, E. D., and N. H. Russell. 1999. The consistency of individual differences in behaviour: temperature effects on antipredator behaviour in garter snakes. Anim. Behav. 57:445-451.
    Bronikowski, A. M. 2000. Experimental evidence for the adaptive evolution of growth rate in the garter snake Thamnophis elegans. Evolution 54:1760-1767.
    Bronikowski, A. M., and S. J. Arnold. 1999. The evolutionary ecology of life history variation in the garter snake Thamnophis elegans. Ecology 80:2314-2325.
    Brown, G. P., and P. J. Weatherhead. 1997. Effects of reproduction on survival and growth of female northern water snakes, Nerodia sipedon. Can. J. Zool. 75:424-432.
    Brown, G. P., and P. J. Weatherhead. 1999a. Demography and sexual size dimorphism in northern water snakes, Nerodia sipedon. Can. J. Zool. 77:1358-1366.
    Brown, G. P., and P. J. Weatherhead. 1999b. Growth and sexual size dimorphism in northern water snakes (Nerodia sipedon). Copeia 1999:723-732.
    Brown, G. P., and P. J. Weatherhead. 2004. Sexual abstinence and the cost of reproduction in adult male water snakes, Nerodia sipedon. Oikos 104:269-276.
    Brown, W. S. 1991. Female reproductive ecology in a northern population of the timber rattlesnake, Crotalus horridus. Herpetologica 47:101-115.
    Burns, G., and H. Heatwole. 2000. Growth, sexual dimorphism, and population biology of the olive sea snake, Aipysurus laevis, on the Great Barrier Reef of Australia. Amphibia-Reptilia 21:289-300.
    Charland, M. B., and P. T. Gregory. 1995. Movements and habitat use in gravid and nongravid female garter snakes (Colubridae, Thamnophis). J. Zool. 236:543-561.
    Christian, K., C. R. Tracy, and W. P. Porter. 1983. Seasonal shifts in body-temperature and use of microhabitats by Galapagos land iguanas (Conolophus pallidus). Ecology 64:463-468.
    Clark, D. L., and J. C. Gillingham. 1990. Sleep-site fidelity in 2 Puerto-Rican lizards. Anim. Behav. 39:1138-1148.
    Clutton-Brock, T. H. 1991. The evolution of parental care. Princeton University Press, New Jersey.
    Creer, S., W. H. Chou, A. Malhotra, and R. S. Thorpe. 2002. Offshore insular variation in the diet of the Taiwanese bamboo viper Trimeresurus stejnegeri (Schmidt). Zool. Sci. 19:907-913.
    Darwin, C. 1871. The descent of man and selection in relation to sex. John Murray, London.
    Dial, B. E. 1978. Thermal ecology of 2 sympatric, nocturnal Coleonyx (Lacertilia Gekkonidae). Herpetologica 34:194-201.
    Diller, L. V., and R. L. Wallace. 2002. Growth, reproduction, and survival in a population of Crotalus viridis oreganus in north central Idaho. Herpetol. Monogr. 16:26-45.
    Downes, S. 1999. Prey odor influences retreat-site selection by naive broadheaded snakes (Hoplocephalus bungaroides). J. Herpetol. 33:156-159.
    Downes, S. 2001. Trading heat and food for safety: costs of predator avoidance in a lizard. Ecology 82:2870-2881.
    Downes, S., and R. Shine. 1998. Heat, safety or solitude? Using habitat selection experiments to identify a lizard's priorities. Anim. Behav. 55:1387-1396.
    Dunham, A. E., D. B. Miles, and D. N. Reznick. 1988. Life history patterns in squamate reptiles. Pages 441-522 in C. Gans and R. B. Huey, editors. Biology of the Reptilia, Vol. 16. John Wiley and Sons, New York.
    Fitch, H. S. 1991. Reproductive cycles of lizards and snakes. The University of Kansas Museum of Natural History.
    Fitzgerald, M., R. Shine, and F. Lemckert. 2002. Radiotelemetric study of habitat use by the arboreal snake Hoplocephalus stephensii (Elapidae) in eastern Australia. Copeia 2002:321-332.
    Fitzgerald, M., R. Shine, and F. Lemckert. 2003. A reluctant heliotherm: thermal ecology of the arboreal snake Hoplocephalus stephensii (Elapidae) in dense forest. J. Therm. Biol. 28:515-524.
    Fitzgerald, M., R. Shine, F. Lemckert, and A. Towerton. 2005. Habitat requirements of the threatened snake species Hoplocephalus stephensii (Elapidae) in eastern Australia. Austral. Ecol. 30:465-474.
    Flatt, T., S. Dummermuth, and A. B. R. 1997. Mark-recapture estimates of survival in populations of the asp viper, Vipera aspis aspis. J. Herpetol. 31:558-564.
    Ford, N. B., and G. M. Burghardt. 1993. Perceptual mechanisms and the behavioral ecology of snakes. Pages 117-164 in R. A. Seigel and J. T. Collins, editors. Snakes: ecology and behavior. McGraw-Hill, New York.
    Ford, N. B., and R. A. Seigel. 1989. Relationships among body size, clutch size, and egg size in 3 species of oviparous snakes. Herpetologica 45:75-83.
    Ford, N. B., and R. A. Seigel. 1994. An experimental-study of the trade-offs between age and size at maturity - effects of energy availability. Funct. Ecol. 8:91-96.
    Forsman, A. 1993. Survival in relation to body-size and growth-rate in the adder, Vipera-Berus. J. Anim. Ecol. 62:647-655.
    Forsman, A. 1995. Opposing fitness consequences of colour pattern in male and female snakes. J. Evol. Biol. 8:53-70.
    Forsman, A. 1997. Growth and survival of Vipera berus in a variable environment. Pages 143-153 in R. S. Thrope, W. Wuster, and A. Malhotra, editors. Venomous snakes: ecology, evolution and snakebite. Oxford University Press, New York.
    Fukada, H. 1978. Growth and maturity of Japanese rat snake, Elaphe climacophora (Reptilia, Serpentes, Colubridae). J. Herpetol. 12:269-274.
    Gibbons, J. W., and R. D. Semlitsch. 1987. Activity patterns. Pages 396-421 in R. A. Seigel, J. T. Collins, and S. S. Novak, editors. Snakes: ecology and evolutionary biology. McGraw-Hill, New York.
    Gregory, P. T., J. M. Macartney, and K. W. Larsen. 1987. Spatial patterns and movements. Pages 366-395 in R. A. Seigel, J. T. Collins, and S. S. Novak, editors. Snakes: ecology and evolutionary biology. McGraw-Hill, New York.
    Heard, G. W., D. Black, and P. Robertson. 2004. Habitat use by the inland carpet python (Morelia spilota metcalfei:Pythonidae): Seasonal relationships with habitat structure and prey distribution in a rural landscape. Austral. Ecol. 29:446-460.
    Heino, M., and V. Kaitala. 1999. Evolution of resource allocation between growth and reproduction in animals with indeterminate growth. J. Evol. Biol. 12:423-429.
    Henderson, R. W., L. G. Hoevers, and M. A. Nickerson. 1977. Observations and comments on feeding behavior of Leptophis (Reptilia, Serpentes, Colubridae). J. Herpetol. 11:231-232.
    Himes, J. G., L. M. Hardy, D. C. Rudolph, and S. J. Burgdorf. 2002. Growth rates and mortality of the Louisiana pine snake (Pituophis ruthveni). J. Herpetol. 36:683-687.
    Houston, D., and R. Shine. 1994a. Low growth rates and delayed maturation in Arafura filesnakes (Serpentes, Acrochordidae) in Tropical Australia. Copeia 1994:726-731.
    Houston, D., and R. Shine. 1994b. Movements and activity patterns of arafura filesnakes (Serpentes, Acrochordidae) in tropical Australia. Herpetologica 50:349-357.
    Huey, R. B., and J. G. Kingsolver. 1989. Evolution of thermal sensitivity of ectotherm performance. Trends Ecol. Evol. 4:131-135.
    Huey, R. B., C. R. Peterson, S. J. Arnold, and W. P. Porter. 1989. Hot rocks and not-so-hot rocks - retreat-site selection by garter snakes and its thermal consequences. Ecology 70:931-944.
    Huey, R. B., and E. R. Pianka. 1981. Ecological consequences of foraging mode. Ecology 62:991-999.
    Jolly, G. M. 1965. Explicit estimates from capture-recapture data with both death and immigration-stochastic model. Biometrika 52:225-247.
    Jolly, G. M. 1982. Mark-recapture models with parameters constant in time. Biometrics 38:301-321.
    Kearney, M. 2002. Hot rocks and much-too-hot rocks: seasonal patterns of retreat-site selection by a nocturnal ectotherm. J. Therm. Biol. 27:205-218.
    Kearney, M., and M. Predavec. 2000. Do nocturnal ectotherms thermoregulate? A study of the temperate gecko Christinus marmoratus. Ecology 81:2984-2996.
    King, R. B., T. D. Bittner, A. Queral-Regil, and J. H. Cline. 1999. Sexual dimorphism in neonate and adult snakes. J. Zool. 247:19-28.
    Kozlowski, J., and A. T. Teriokhin. 1999. Allocation of energy between growth and reproduction: The Pontryagin Maximum Principle solution for the case of age- and season-dependent mortality. Evol. Ecol. Res. 1:423-441.
    Lebreton, J. D., K. P. Burnham, J. Clobert, and D. R. Anderson. 1992. Modeling survival and testing biological hypotheses using marked animals - a unified approach with case-studies. Ecol. Monogr. 62:67-118.
    Lee, W., and K. Lue. 1996. The preliminary study on the food habits of snakes in Taiwan. Biol. Bull. Natl. Taiwan Normal Univ. 31:119-124.
    Lessells, C. M. 1991. The evolution of life histories. in J. R. Krebs and N. B. Davies, editors. Behavioural ecology: an evolutionary approach. Blackwell Scientific Publications, London.
    Lillywhite, H. B., and R. W. Henderson. 1993. Behavioral and functional ecology of arboreal snakes. Pages 1-48 in R. A. Seigel and J. T. Collins, editors. Snakes: ecology and behavior. McGraw-Hill, New York.
    Lin, H. C., H. Y. Hung, K. Y. Lue, and M. C. Tu. 2006. Diurnal retreat selection by the arboreal Chinese green tree viper (Trimeresurus s. stejnegeri) as influenced by temperature. Zool. Stud.(In press)
    Lin, W. H. 2005. A review of the breeding ecology of the crested serpent eagle ( Spilornis cheela ) in the Taipei area. Raptor Res. Taiwan 5:31-44.
    Losos, J. B. 1987. Postures of the military dragon (Ctenophorus isolepis) in relation to substrate temperature. AMPHIBIA-REPTILIA 8:419-423.
    Lourdais, O., X. Bonnet, R. Shine, D. Denardo, G. Naulleau, and M. Guillon. 2002. Capital-breeding and reproductive effort in a variable environment: A longitudinal study of a viviparous snake. J. Anim. Ecol. 71:470-479.
    Luiselli, L., M. Capula, and R. Shine. 1996. Reproductive output, costs of reproduction, and ecology of the smooth snake, Coronella austriaca, in the eastern Italian Alps. Oecologia 106:100-110.
    Madsen, T. 1987. Cost of reproduction and female life-history tactics in a population of grass snakes, Natrix Natrix, in Southern Sweden. Oikos 49:129-132.
    Madsen, T., and R. Shine. 1992. Determinants of reproductive success in female adders, Vipera-Berus. Oecologia 92:40-47.
    Madsen, T., and R. Shine. 1993a. Costs of reproduction in a population of European adders. Oecologia 94:488-495.
    Madsen, T., and R. Shine. 1993b. Phenotypic plasticity in body sizes and sexual size dimorphism in European grass snakes. Evolution 47:321-325.
    Madsen, T., and R. Shine. 1994. Costs of reproduction influence the evolution of sexual size dimorphism in snakes. Evolution 48:1389-1397.
    Madsen, T., and R. Shine. 1999. The adjustment of reproductive threshold to prey abundance in a capital breeder. J. Anim. Ecol. 68:571-580.
    Madsen, T., and R. Shine. 2000a. Energy versus risk: costs of reproduction in free-ranging pythons in tropical Australia. Austral. Ecol. 25:670-675.
    Madsen, T., and R. Shine. 2000b. Silver spoons and snake body sizes: Prey availability early in life influences long-term growth rates of free-ranging pythons. J. Anim. Ecol. 69:952-958.
    Madsen, T., R. Shine, J. Loman, and T. Hakansson. 1992. Why do female adders copulate so frequently. Nature 355:440-441.
    Madsen, T., R. Shine, J. Loman, and T. Hakansson. 1993. Determinants of mating success in male adders, Vipera-Berus. Anim. Behav. 45:491-499.
    Mao, S. H. 1962. Sexual dimorphism of Taiwan bamboo vipers. B. I. Zool. Acad. Sinica 1:41-46.
    Mao, S. H. 1970. Food of the common venomous snakes of Taiwan. Herpetologica 26:45-48.
    Masunaga, G., and H. Ota. 2003. Growth and reproduction of the sea snake, Emydocephalus ijimae, in the central Ryukyus, Japan: a mark and recapture study. Zool. Sci. 20:461-470.
    May, P. G., T. M. Farrell, S. T. Heulett, M. A. Pilgrim, L. A. Bishop, D. J. Spence, A. M. Rabatsky, M. G. Campbell, A. D. Aycrigg, and W. E. Richardson. 1996. Seasonal abundance and activity of a rattlesnake (Sistrurus miliarius barbouri) in central Florida. Copeia 1996:389-401.
    Mertens, D. 1995. Population-structure and abundance of grass snakes, Natrix Natrix, in Central Germany. J. Herpetol. 29:454-456.
    Mullin, S. J., and R. J. Cooper. 2000. The foraging ecology of the gray rat snake (Elaphe obsoleta spiloides). II. Influence of habitat structural complexity when searching for arboreal avian prey. Amphibia-Reptilia 21:211-222.
    Mullin, S. J., R. J. Cooper, and W. H. N. Gutzke. 1998. The foraging ecology of the gray rat snake (Elaphe obsoleta spiloides). III. Searching for different prey types in structurally varied habitats. Can. J. Zool. 76:548-555.
    Nishimura, M., and S. Katsuren. 1994. Annual survival rate and age structure of habu, Trimeresurus flavoviridis (Viperidae), on Minna island, Japan - estimation from removal trapping. Res. Popul. Ecol. 36:255-260.
    Olsson, M., and R. Shine. 1996. Does reproductive success increase with age or with size in species with indeterminate growth? A case study using sand lizards (Lacerta agilis). Oecologia 105:175-178.
    Parent, C., and P. J. Weatherhead. 2000. Behavioral and life history responses of eastern massasauga rattlesnakes (Sistrurus catenatus catenatus) to human disturbance. Oecologia 125:170-178.
    Parker, W. S., and M. V. Plummer. 1987. Population ecology. Pages 253-301 in R. A. Seigel, J. T. Collins, and S. S. Novak, editors. Snakes: ecology and evolutionary biology. McGraw-Hill, New York.
    Peterson, C. R., A. R. Gibson, and M. E. Dorcas. 1993. Snake thermal ecology: the causes and consequences of body-temperature variation. Pages 241-314 in R. A. Seigel and J. T. Collins, editors. Snakes: ecology and behavior. McGraw-Hill, New York.
    Plummer, M. V. 1992. Relationships among mothers, litters, and neonates in diamondback water snakes (Nerodia-Rhombifer). Copeia:1096-1098.
    Plummer, M. V. 1997. Population ecology of green snakes (Opheodrys aestivus) revisited. Herpetol. Monogr. 11:102-123.
    Pringle, R. M., J. K. Webb, and R. Shine. 2003. Canopy structure, microclimate, and habitat selection by a nocturnal snake, Hoplocephalus bungaroides. Ecology 84.
    Prival, D. B., M. J. Goode, D. E. Swann, C. R. Schwalbe, and M. J. Schroff. 2002. Natural history of a northern population of twin-spotted rattlesnakes, Crotalus pricei. J. Herpetol. 36:598-607.
    Qualls, C. P., and R. Shine. 1998. Costs of reproduction in conspecific oviparous and viviparous lizards, Lerista bougainvillii. Oikos 82:539-551.
    Reading, C. J. 2004. Age, growth and sex determination in a population of smooth snakes, Coronella austriaca in southern England. Amphibia-Reptilia 25:137-150.
    Reaney, L. T., and M. J. Whiting. 2003. Picking a tree: habitat use by the tree agama, Acanthocercus atricollis atricollis, in South Africa. Afr. Zool. 38:273-278.
    Reinert, H. K. 1993. Habitat selection in snakes. Pages 201-240 in R. A. Seigel and J. T. Collins, editors. Snakes: ecology and behavior. McGraw-Hill, New York.
    Reinert, H. K., D. Cundall, and L. M. Bushar. 1984. Foraging behavior of the timber rattlesnake, Crotalus-Horridus. Copeia 1984:976-981.
    Reinert, H. K., and R. T. Zappalorti. 1988. Timber rattlesnakes (Crotalus-Horridus) of the pine barrens - Their movement patterns and habitat preference. Copeia 1988:964-978.
    Roff, D. A. 1992. The evolution of life histories. Chapman Hall, New York.
    Rutherford, P. L. 2004. Proximate mechanisms that contribute to female-biased sexual size dimorphism in an anguid lizard. Can. J. Zool. 82:817-822.
    Schwarzkopf, L. 2005. Sexual dimorphism in body shape without sexual dimorphism in body size in water skinks (Eulamprus quoyii). Herpetologica 61:116-123.
    Seber, G. A. F. 1965. Anote on the multiple recapture cencus. Biometrika 52:249-259.
    Seigel, R. A. 1993. Summary: Future research on snakes, or how to combat "lizard envy". Pages 395-402 in R. A. Seigel and J. T. Collins, editors. Snakes: ecology and behavior. McGraw-Hill, New York.
    Seigel, R. A., and N. B. Ford. 1987. Reproductive ecology. Pages 210-252 in R. A. Seigel, J. T. Collins, and S. S. Novak, editors. Snakes:Ecology and Evolutionary Biology. McGraw-Hill, New York.
    Shah, B., R. Shine, S. Hudson, and M. Kearney. 2004. Experimental analysis of retreat-site selection by thick-tailed geckos Nephrurus milii. Austral. Ecol. 29:547-552.
    Shine, R. 1978. Sexual size dimorphism and male combat in snakes. Oecologia 33:269-277.
    Shine, R. 1980. Costs of reproduction in reptiles. Oecologia 46:92-100.
    Shine, R. 1988. The evolution of large body size in females - a critique of Darwins fecundity advantage model. Am. Nat. 131:124-131.
    Shine, R. 1990. Proximate determinants of sexual differences in adult body size. Am. Nat. 135:278-283.
    Shine, R. 1993. Sexual dimorphism in snakes. Pages 49-86 in R. A. Seigel and J. T. Collins, editors. Snakes:ecology and behavior. McGraw-Hill, New York.
    Shine, R. 1994. Sexual size dimorphism in snakes revisited. Copeia 1994:326-346.
    Shine, R. 2003. Reproductive strategies in snakes. Proc. R. Soc. Ser. B-Bio 270:995-1004.
    Shine, R., and X. Bonnet. 2000. Snakes: a new 'model organism' in ecological research? Trends Ecol. Evol. 15:221-222.
    Shine, R., and E. L. Charnov. 1992. Patterns of survival, growth, and maturation in snakes and lizards. Am. Nat. 139:1257-1269.
    Shine, R., and R. Lambeck. 1985. A radiotelemetric study movements, thermoregulation and habitat utilization of Arafura filesnakes (Serpentes, Acrochordidae). Herpetologica 41:351-361.
    Shine, R., M. M. Olsson, M. P. Lemaster, I. T. Moore, and R. T. Mason. 2000. Effects of sex, body size, temperature, and location on the antipredator tactics of free-ranging gartersnakes (Thamnophis sirtalis, Colubridae). Behav. Ecol. 11:239-245.
    Shine, R., and L. Schwarzkopf. 1992. The evolution of reproductive effort in lizards and snakes. Evolution 46:62-75.
    Shine, R., and L. X. Sun. 2002. Arboreal ambush site selection by pit-vipers Gloydius shedaoensis. Anim. Behav. 63:565-576.
    Shine, R., L. X. Sun, M. Kearney, and M. Fitzgerald. 2002. Why do juvenile Chinese pit-vipers (Gloydius shedaoensis) select arboreal ambush sites? Ethology 108:897-910.
    Stanford, K. M., and R. B. King. 2004. Growth, survival, and reproduction in a northern Illinois population of the plains garter snake, Thamnophis radix. Copeia 2004:465-478.
    Stapley, J. 2003. Differential avoidance of snake odours by a lizard: evidence for prioritized avoidance based on risk. Ethology 109:785-796.
    Stearns, S. C. 1992. The evolution of life histories. Oxford University Press, New York.
    Sun, L. X., R. Shine, D. B. Zhao, and Z. R. Tang. 2002. Low costs, high output: reproduction in an insular pit-viper (Gloydius shedaoensis, Viperidae) from north-eastern China. J. Zool. 256:511-521.
    Taborsky, B., U. Dieckmann, and M. Heino. 2003. Unexpected discontinuities in life-history evolution under size-dependent mortality. Proc. R. Soc. Ser. B-Bio 270:713-721.
    Taylor, E. N., and D. F. Denardo. 2005. Sexual size dimorphism and growth plasticity in snakes: an experiment on the Western Diamond-backed Rattlesnake (Crotalus atrox). J. Exp. Zool. Part. A. 303A:598-607.
    Theodoratus, D. H., and D. Chiszar. 2000. Habitat selection and prey odor in the foraging behavior of western rattlesnakes (Crotalus viridis). Behaviour 137:119-135.
    Tsai, T. S., and M. C. Tu. 1998. Sexual dimorphism of Chinese green tree viper, Treimeresurus stejnegeri stejnegeri. Biol. Bull. Natl. Taiwan Normal Univ. 33:13-22.
    Tsai, T. S., and M. C. Tu. 2000. Reproductive cycle of male Chinese green tree vipers, Trimeresurus s. stejnegeri, in northern Taiwan. J. Herpetol. 34:424-430.
    Tsai, T. S., and M. C. Tu. 2001. Reproductive cycle of female Chinese green tree vipers, Trimeresurus stejnegeri stejnegeri, in northern Taiwan. Herpetologica 57:157-168.
    Tsai, T. S., and M. C. Tu. 2005. Postprandial thermophily of Chinese green tree vipers, Trimeresurus s. stejnegeri: interfering factors on snake temperature selection in a thigmothermal gradient. J. Therm. Biol. 30:423-430.
    Tsairi, H., and A. Bouskila. 2004. Ambush site selection of a desert snake (Echis coloratus) at an oasis. Herpetologica 60:13-23.
    Tu, M.-C., S. W. Wang, and Y.-C. Lin. 2000. No divergence of habitat selection between male and female arboreal snakes, Trimeresurus s. stejnegeri. Zool. Stud. 39:91-98.
    Ujvari, B., Z. Korsos, and T. Pechy. 2000. Life history, population characteristics and conservation of the Hungarian meadow viper (Vipera ursinii rakosiensis). Amphibia-Reptilia 21:267-278.
    Voris, H. K., and B. C. Jayne. 1979. Growth, reproduction and population-structure of a marine snake, Enhydrina schistosa (Hydrophiidae). Copeia 1979:307-318.
    Wallace, R. L., and L. V. Diller. 1990. Feeding ecology of the rattlesnake, Crotalus viridis oreganus, in northern Idaho. J. Herpetol. 24:246-253.
    Wang, S. A. 1999. Study on the skewed ratio of Chinese green tree viper, Trimeresurus s. stejnegeri, at Tsao-chiao area. Master's thesis. National Taiwan Normal Univ., Taipei.
    Wang, S. A., H. C. Lin, and M. C. Tu. 2003. Skewed sex ratio of the Chinese green tree viper, Trimeresurus stejnegeri stejnegeri, at Tsaochiao, Taiwan. Zool. Stud. 42:379-385.
    Watkins, G. G. 1996. Proximate causes of sexual size dimorphism in the iguanian lizard Microlophus occipitalis. Ecology 77:1473-1482.
    Webb, J. K., B. W. Brook, and R. Shine. 2002a. What makes a species vulnerable to extinction? Comparative life-history traits of two sympatric snakes. Ecol. Res. 17:59-67.
    Webb, J. K., K. A. Christian, and P. Fisher. 2002b. Fast growth and early maturation in a viviparous sit-and-wait predator, the northern death adder (Acanthophis praelongus), from tropical Australia. J. Herpetol. 36:505-509.
    Webb, J. K., R. M. Pringle, and R. Shine. 2004. How do nocturnal snakes select diurnal retreat sites? Copeia 2004:919-925.
    Webb, J. K., and R. Shine. 1997a. A field study of spatial ecology and movements of a threatened snake species, Hoplocephalus bungaroides. Biol. Conserv. 82:203-217.
    Webb, J. K., and R. Shine. 1997b. Out on a limb: Conservation implications of tree-hollow use by a threatened snake species (Hoplocephalus bungaroides: Serpentes, Elapidae). Biol. Conserv. 81:21-33.
    Webb, J. K., and R. Shine. 1998a. Thermoregulation by a nocturnal elapid snake (Hoplocephalus bungaroides) in southeastern Australia. Physiol. Zool. 71:680-692.
    Webb, J. K., and R. Shine. 1998b. Using thermal ecology to predict retreat-site selection by an endangered snake species. Biol. Conserv. 86:233-242.
    Xiao, Z. W. 2000. Study on the activity pattern and methodology of movement of male Chinese green tree viper, Trimeresurus s. stejnegeri. Master's thesis. National Taiwan Univ., Taipei, Taiwan.
    Zug, G. R. 1993. Herpetology: an introductory biology of amphibians and reptiles. Academic Press, San Diego.

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