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Ecological patterns of relative clutch mass in snakes

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Summary

Data on the relative clutch mass of snakes are summarized for over 100 populations. RCM was significantly lower in live bearing versus egg laying forms. We suggest that the longer reproductive season of viviparous snakes results in higher overall mortality compared to oviparous species; by reducing RCM, viviparous snakes may reduce this risk of mortality. Unlike lizards, no differences in RCM were found between categories of either escape behavior or foraging mode, possibly because detailed information on these behaviors are lacking for most snakes. In four populations examined, RCM did not vary among years. When compared to lizards, snakes demonstrate significantly higher RCM, perhaps owing to a more energetically efficient means of locomotion. Our data support the contention that RCM should be considered a separate and distinctive life-history characteristic of reptiles.

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References

  • Aldridge RD (1979) Female reproductive cycles of the snakes Arizona elegans and Crotalus viridis. Herpetologica 35:256–261

    Google Scholar 

  • Armstrong BL, Murphy JB (1979) The natural history of Mexican rattlesnakes. Spec Publ Mus Nat Hist, Univ. Kansas 5:1–88

    Google Scholar 

  • Assetto R Jr (1978) Reproduction of the gray-banded kingsnake, Lampropeltis mexicana alterna. Herpetol Rev 9:56–57

    Google Scholar 

  • Bauwens D, Thoen C (1981) Escape tactics and vulnerability to predation associated with reproduction in the lizard Lacerta vivipara. J Anim Ecol 50:733–743

    Google Scholar 

  • Branson BA, Baker EC (1974) An ecological study of the Queen snake, Regina septemvittata (Say) in Kentucky. Tul Stud Zool and Bot 18:153–171

    Google Scholar 

  • Brockelman WY (1975) Competition, the fitness of offspring, and optimal clutch size. Am Nat 109:677–699

    Google Scholar 

  • Bull JJ, Shine R (1979) Iteroparous animals that skip opportunities for reproduction. Am Nat 114:296–303

    Google Scholar 

  • Campbell JA (1973) A captive hatching of Micrurus fulvius tenere (Serpents, Elapidae). J Herpetol 7:312–315

    Google Scholar 

  • Carpenter CC (1960) A large brood of western pygmy rattlesnakes. Herpetologica 16:142–143

    Google Scholar 

  • Chiras S (1982) Captive reproduction of the Children's python, Liasis childreni. Herpetol Rev 13:14–15

    Google Scholar 

  • Clark DR JR (1974) The western ribbon snake (Thamnophis proximus): Ecology of a Texas population. Herpetologica 30: 372–379

    Google Scholar 

  • Clark DR JR, Lieb CS (1973) Notes on reproduction in the night snake (Hypsiglena torquata). Southwest Nat 18:248–252

    Google Scholar 

  • Clark H (1953) Eggs, egg-laying and incubation of the snake Elaphe emoryi (Barid and Girard). Copeia 1953:90–92

    Google Scholar 

  • Conant R (1938) A note on eggs and young of Leioheterodon madagacariensis (Dumeril and Bibron). Zoologica 23:389–391

    Google Scholar 

  • Conant R (1942) Notes on the young of three recently described snakes, with comments on their relationships. Bull Chicago Acad Sci 6:193–200

    Google Scholar 

  • Conant R (1943) Studies on North American water snakes-I Natrix kirtlandi (Kennicott). Am Midl Nat 29:313–341

    Google Scholar 

  • Conant R (1965) Notes on reproduction in two natricine snakes from Mexico. Herpetologica 21:140–144

    Google Scholar 

  • Conant R (1975) A field guide to reptiles and amphibians of eastern and central North America. Houghton Mifflin Company, Boston

    Google Scholar 

  • Conant R, Downs A Jr (1940) Miscellaneous notes on the eggs and young of reptiles. Zoologica 25:33–40

    Google Scholar 

  • Derickson WK (1976) Ecological and physiological aspects of reproductive strategies in two lizards. Ecology 57:445–458

    Google Scholar 

  • Dmi'el R (1967) Studies on reproduction, growth, and feeding in the snake Spalerosophis cliffordi (Colubridae). Copeia 1967: 332–346

    Google Scholar 

  • Droge DL, Jones SM, Ballinger RE (1982) Reprodution of Holbrookia maculata in western Nebraska. Copeia 1982:356–362

    Google Scholar 

  • Dundee HA (1950) Additional records of Hypsiglena from Oklahoma, with notes on the behavior and the eggs. Herpetologica 6:28–30

    Google Scholar 

  • Dunham AE (1982) Demographic and life-history variation among populations of the iguanid lizard Urosaurus ornatus: implications for the study of life-history phenomena in lizards. Herpetologica 38:208–221

    Google Scholar 

  • Feaver PE (1977) The demography of a Michigan population of Natrix sipedon with discussions of ophidian growth and repoduction. Ph.D. Dissertation, Univ. Michigan

  • Ferguson GW, Bohlen CH (1978) Demographic analysis: a tool for the study of natural selection of behavior traits. In: Behavior and neurobiology of lizards. Greenburg N, MacLean PD (eds), pp 227–240

  • Fitch H (1970) Reproductive cycles in lizards and snakes. Univ. Kansas Mus Nat Hist Misc Publ 42:1–247

    Google Scholar 

  • Fleet RR, Kroll JC (1978) Litter size and parturition behavior in Sistrurus miliarius streckeri. Herpetol Rev 9:11

    Google Scholar 

  • Fukada H (1963) Eggs and young of Dinodon orientale (Hilgendorf). Biological studies on the snakes. X. Bull Kyoto Gakugei Univ, Ser B 20:12–17

    Google Scholar 

  • Funk RS, Tucker JK (1978) Variation in a large brood of lined snakes, Tropidoclonion lineatum (Reptilia, Serpentes, Colubridae). J Herpetol 12:115–117

    Google Scholar 

  • Gloyd HK, Conant R (1934) The taxonomic status, range, and natural history of Schott's racer. Occ Pap Mus Zool, Univ. Michigan 287:1–17

    Google Scholar 

  • Grimpe RD, Benefield GE (1981) Life history notes: Lampropeltis g. holbrooki. Herpetol Rev 12:80

    Google Scholar 

  • Hirshfield MF, Tinkle DW (1975) Natural selection and the evolution of reproductive effort. Proc Nat Acad Sci, USA 72: 2227–2231

    Google Scholar 

  • Holstrom WF Jr (1980) Observations on the reproduction of the common anaconda, Eunectes murinus, at the New York Zoological Park. Herpetol Rev 11:32–33

    Google Scholar 

  • Huey RB, Pianka ER (1981) Ecological consequences of foraging mode. Ecology 62:991–999

    Google Scholar 

  • Hunt LE, Ottley JR (1982) Reproduction and feeding in Eridiphas sleveni (Serpentes: Colubridae). Herpetol Rev 13:8–9

    Google Scholar 

  • Jones L (1976) A large brood for a Maryland Storeia dekayi dekayi. Bull Maryland Herpetol Soc 12:102–103

    Google Scholar 

  • Kennedy JP (1961) Eggs of the eastern hognose snake, Heterodon platyrhinos. Texas J Sci 13:416–422

    Google Scholar 

  • Kennedy JP (1964) Natural history notes on some snakes of eastern Texas. Texas J Sci 16:210–215

    Google Scholar 

  • Lee DS (1967) Eggs and hatchlings of the Florida pine snake, Pituophis melanoleucus mugitus. Herpetologica 23:241–242

    Google Scholar 

  • Lemen CA, Voris HK (1981) A comparison of reproductive strategies among marine snakes. J Anim Ecol 50:89–101

    Google Scholar 

  • Martin BE (1975) Notes on a brood of the Arizona ridge-nosed rattlesnake. Bull Maryland Herpetol Soc 11:64–65

    Google Scholar 

  • Martin BE (1976) Notes on the breeding behavior in a captive pair of Sonora mountain kingsnakes, (Lampropeltis pyromelana). Bull Maryland Herpetol Soc 12:23–24

    Google Scholar 

  • Martin RF (1977) Variation in reproductive productivity of range margin tree lizards (Urosaurus ornatus). Copeia 1977:83–92

    Google Scholar 

  • Mendelssohn H (1963) On the biology of the venomous snakes of Israel. I. Israel J Zool 12:143–170

    Google Scholar 

  • Mendelssohn H (1965) On the biology of the venomous snakes of Israel. II. Israel J Zool 14:185–212

    Google Scholar 

  • Munro DF (1949) Gain in size and weight of Heterodon eggs during incubation. Herpetologica 5:133–134

    Google Scholar 

  • Murphy JB, Barker DG, Tryon BW (1978) Miscellaneous notes on the reproductive biology of reptiles. 2. Eleven species of the Family Boidae, genera Candoia, Corallus, Epicrates, and Python. J Herpetol 12:385–390

    Google Scholar 

  • Naulleau G, Brule B van den (1980) Captive reproduction of Vipera russelli (Shaw, 1797). Herpetol Rev 11:110–112

    Google Scholar 

  • Neill WT (1964) Viviparity in snakes: some ecological and zoogeographical considerations. Am Nat 98:35–55

    Google Scholar 

  • Parker WS, Brown WS (1980) Comparative ecology of two colubrid snakes, Masticophis t. taeniatus and Pituophis melanoleucus deserticola, in northern Utah.Contr Biol. Geol, Milwaukee Pub Mus 7:1–104

    Google Scholar 

  • Patterson JW, Davies PMC (1982) Predatory behavior and temperature relations in the snake Natrix maura. Copeia 1982:472–474

    Google Scholar 

  • Pianka ER (1973) The structure of lizard communities. Ann Rev Ecol Syst 4:53–74

    Google Scholar 

  • Pianka ER, Parker WS (1975) Ecology of horned lizards: a review with special reference to Phrynosoma platyrhinos. Copeia 1975:141–162

    Google Scholar 

  • Plummer MV (1984) Female reproduction in an Arkansas population of rough green snakes (Opheodrys aestivus). In: Seigel RA (eds) Vertebrate ecology and systematics. A tribute to Henry S. Fitch. Spec Publ Mus Nat Hist, Univ. of Kansas. 10

  • Prestt I (1971) An ecological study of the viper Vipera berus in southern Britain. J Zool London 164:373–418

    Google Scholar 

  • Semlitsch RD, Gibbons JW (1978) Reproductive allocation in the brown water snake, Natrix taxispilota. Copeia 1978:721–723

    Google Scholar 

  • Shine R (1980) “Costs” of reproduction in reptiles. Oecologia (Berlin) 46:92–100

    Google Scholar 

  • Shine R, Bull JJ (1979) The evolution of live-bearing in lizards and snakes. Am Nat 113:905–923

    Google Scholar 

  • Stearns SC (1976) Life-history tactics: a review of the ideas. Quart Rev Biol 51:3–47

    Google Scholar 

  • Swingland IR, Coe MJ (1979) The natural regulation of giant tortoise populations on Aldabra Atoll: Recruitment. Philos Trans Royal Soc London, Ser B 286:177–188

    Google Scholar 

  • Tinkle DW, Hadley NF (1975) Lizard reproductive effort: caloric estimates and comments on its evolution. Ecology 56:427–434

    Google Scholar 

  • Tinkle DW, Gibbons JW (1977) The distribution and evolution of viviparity in reptiles. Misc Publ, Mus Zool, Univ. Michigan 154:1–55

    Google Scholar 

  • Tinkle DW (1969) The concept of reproductive effort and its relation to the evolution of life histories in lizards. Am Nat 103:501–516

    Google Scholar 

  • Tryon BW, McCrystal HK (1982) Life history notes: Micrurus fulvius tenere. Herpetol Rev 13:47–48

    Google Scholar 

  • Tryon BW, Murphy JB (1982) Miscellaneous notes on the reproductive biology of reptiles. 5. Thirteen varieties of the genus Lampropeltis, species mexicana, triangulum and zonata. Trans Kansas Acad Sci 85:96–119

    Google Scholar 

  • Tryon BW, Radcliffe CW (1977) Reproduction in captive lower California rattlesnakes, Crotalus enyo enyo (Cope). Herpetol Rev 8:34–36

    Google Scholar 

  • Tucker JK (1976) Observations on the birth of a brood of Kirtland's water snake, Clonophis kirtlandi (Kennicott). (Reptilia, Serptentes, Colubridae). J Herpetol 10:53–54

    Google Scholar 

  • Van Mierop LHS, Bessette EL (1981) Reproduction of the ball python, Python regius in captivity. Herpetol Rev 12:20–22

    Google Scholar 

  • Vitt LJ (1975) Observations on reproduction in five species of Arizona snakes. Herpetologica 31:83–84

    Google Scholar 

  • Vitt LJ (1978) Caloric content of lizard and snake (Reptilia) eggs and bodies and the conversion of weight to caloric data. J Herpetol 12:65–72

    Google Scholar 

  • Vitt LJ (1980) Ecological observations on sympatric Philodryas (Colubridae) in northeastern Brazil. Papeis Avulsos Zool, San Paulo. 34:87–98

    Google Scholar 

  • Vitt LJ (1981) Lizard reproduction: Habitat specificity and constraints on relative clutch mass. Am Nat 117:506–514

    Google Scholar 

  • Vitt LJ, Congdon JD (1978) Body shape, reproductive effort, and relative clutch mass in lizards: resolution of a paradox. Am Nat 112:595–608

    Google Scholar 

  • Vitt LJ, Price HJ (1982) Ecological and evolutionary determinants of relative clutch mass in lizards. Herpetologica 38:237–255

    Google Scholar 

  • Williams GC (1966) Adaptation and natural selection. Princeton University Press, Princeton, N.J.

    Google Scholar 

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Seigel, R.A., Fitch, H.S. Ecological patterns of relative clutch mass in snakes. Oecologia 61, 293–301 (1984). https://doi.org/10.1007/BF00379625

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