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A. Fabien, X. Bonnet, S. Maumelat, D. Bradshaw, T. Schwaner (2004)
Diet divergence, jaw size and scale counts in two neighbouring populations of tiger snakes (Notechis scutatus)Amphibia-reptilia, 25
R. Shine (1980)
“Costs” of reproduction in reptilesOecologia, 46
T. Madsen (1987)
Cost of reproduction and female life-history tactics in a population of grass snakes, Natrix natrix, in southern SwedenOikos, 49
I. Robertson (1992)
Thermal constraints on swimming performance and escape response of northern water snakes (Nerodia sipedon)Canadian Journal of Zoology, 70
C. Cans (1986)
LOCOMOTION OF LIMBLESS VERTEBRATES: PATTERN AND EVOLUTION
C. Andrén (1985)
Risk of predation in male and female adders, Vipera berus (Linné)Amphibia-reptilia, 6
T. Garland, S. Arnold (1983)
Effects of a Full Stomach on Locomotory Performance of Juvenile Garter Snakes (Thamnophis elegans)Copeia, 1983
T. Garland, P. Else (2002)
Seasonal, sexual, and individual variation in endurance and activity metabolism in lizards
B. Sinervo, Richard Hedges, S. Adolph (1991)
Decreased Sprint Speed as a Cost of Reproduction in the Lizard Sceloporus Occidentalis: Variation among PopulationsThe Journal of Experimental Biology, 155
(1999)
Sea snakes. Sydney
(1985)
fast swimming along the length of pool and turns at each ends
Received: November 12, 2003
R. Shine (2003)
Effects of pregnancy on locomotor performance: an experimental study on lizardsOecologia, 136
(1996)
Habitat utilization, movements, and activity patterns of Enhydris plumbea (Ser-pentes: Homalopsinae) in a rice paddy wetland in Bor-neo
Olsson, Shine, Bak‐Olsson (2000)
Locomotor impairment of gravid lizards: is the burden physical or physiological?Journal of Evolutionary Biology, 13
D. Bauwens, C. Thoen (1981)
Escape Tactics and Vulnerability to Predation Associated with Reproduction in the Lizard Lacerta viviparaJournal of Animal Ecology, 50
B. Jayne, Kiew Heang, H. Voris (1988)
Diet, feeding behavior, growth, and numbers of a population of Cerberus rynchops (Serpentes: Homalopsinae) in Malaysia /
B. Jayne (1985)
Swimming in constricting (Elaphe g. guttata) and nonconstricting (Nerodia fasciata pictiventris) colubrid snakesCopeia, 1985
R. Shine (1988)
CONSTRAINTS ON REPRODUCTIVE INVESTMENT: A COMPARISON BETWEEN AQUATIC AND TERRESTRIAL SNAKESEvolution, 42
C. Andrén (1982)
Effect of Prey Density on Reproduction, Foraging and Other Activities in the Adder, Vipera berusAmphibia-reptilia, 3
M. Ladyman, Don Bradshaw (2003)
The influence of dehydration on the thermal preferences of the Western tiger snake, Notechis scutatusJournal of Comparative Physiology B, 173
(1992)
Snakes of Australia: dangerous and harmless
R. Seigel, M. Huggins, N. Ford (1987)
Reduction in locomotor ability as a cost of reproduction in gravid snakesOecologia, 73
Richard Shine, S. Shetty (2001)
Moving in two worlds: aquatic and terrestrial locomotion in sea snakes (Laticauda colubrina, Laticaudidae)Journal of Evolutionary Biology, 14
X. Bonnet, D. Bradshaw, R. Shine, D. Pearson (1999)
Why do snakes have eyes? The (non-)effect of blindness in island tiger snakes (Notechis scutatus)Behavioral Ecology and Sociobiology, 46
H. Voris, B. Jayne (1979)
Growth, Reproduction and Population Structure of a Marine Snake, Enhydrina schistosa (Hydrophiidae)Copeia, 1979
in island tiger snakes
Swimming and pregnancy in Tiger snakes, Notechis scutatus Fabien Aubret 1,2,3 , Xavier Bonnet 1 , Richard Shine 4 , Stéphanie Maumelat 2 Reduced locomotor ability may increase sus- ceptibility to predation and hence may repre- sent a proximate mechanism by which “costs” of reproduction are expressed (Shine, 1980). In squamate reptiles, many examples of such ef- fects have been documented, where non-gravid females and/or males showed higher survival rates than gravid females (Shine, 1980; Andren, 1982, 1985; Madsen, 1987). For instance, preg- nancy may entail a reduction in locomotor per- formances in lizards and snakes (Shine, 1980; Shine, 2003; Bauwens and Thoen, 1981; Gar- land and Else, 1987; Seigel et al., 1987), in- cluding decreased burst speed by 12 to 30%, and endurance by 52 to 55%. Because fleeing from predators or foraging ability depends on speed and/or stamina, reduced locomotor per- formance resulting from carrying offspring may result in increased risk of predation and/or de- creased energy intake compared to non-gravid females. However, less clear is the effect of preg- nancy on aquatic locomotion. Many snakes inhabit aquatic environments such as rivers, lakes, swamps, mangroves, or oceans (Voris and Jayne, 1979; Voris and Karns, 1996; Jayne et
Amphibia-Reptilia – Brill
Published: Jan 1, 2005
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