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The Eastern Massasauga Rattlesnake: - U.S. Fish and Wildlife Service

The Eastern Massasauga Rattlesnake: - U.S. Fish and Wildlife Service

The Eastern Massasauga Rattlesnake: - U.S. Fish and Wildlife Service

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population restrict overwintering activity to a 37 ha peatl<strong>and</strong> within a larger wetl<strong>and</strong> complex<br />

<strong>and</strong> gravid females remain there from spring emergence to parturition as well. Mean 100%<br />

minimum polygon activity range size for gravid females was 2.0 ha. Gravid females moved less<br />

total distance (45.5 m), mean distance per day (7.1 m), <strong>and</strong> less often (45.5% of observations)<br />

than male or nongravid females, who exhibited no differences in these measures. This reduction<br />

in vagility associated with gravidity has been observed in other live-bearing snake species<br />

(Brown et al. 1982, Reinert <strong>and</strong> Zappalorti 1988, Secor 1994, Viitanen 1967, Fitch <strong>and</strong> Shirer<br />

1971). One hypothesis offered to explain this phenomenon is that gravid massasaugas are<br />

selecting a location that maximizes thermoregulatory opportunity to reduce gestation time. King<br />

(1997) also found differences between gravid females <strong>and</strong> males <strong>and</strong> nongravid females in<br />

Wisconsin, although the differences between female groups were not very pronounced. In<br />

Wisconsin, gravid females moved away from overwintering sites following emergence,<br />

presumably to find suitable open-canopy basking sites that were not available near hibernacula.<br />

Weatherhead <strong>and</strong> Prior (1992) found that female massasaugas had significantly smaller activity<br />

ranges <strong>and</strong> other movement parameters than males at their site in Ontario, however, it was<br />

unknown or unclear if any of the females were gravid. Reinert <strong>and</strong> Kodrich (1982) found no<br />

differences between gravid female massasaugas <strong>and</strong> other classes in most movement parameters<br />

in Pennsylvania, however, tracking periods were short <strong>and</strong> snakes were force-fed transmitters,<br />

potentially inducing thermophily <strong>and</strong> reducing movement.<br />

No significant differences were detected between male <strong>and</strong> nongravid female activity<br />

ranges in Cicero Swamp (composite mean 100% activity range = 29 ha) (Johnson 2000). Males<br />

<strong>and</strong> nongravid females did show a difference in range length (812 m for males, 1212 m for<br />

females), which may be explained by the more straight-line, back <strong>and</strong> forth general movement<br />

pattern from emergence to hibernation by the females or simply an artifact of the small sample<br />

size. Males appear to w<strong>and</strong>er more, perhaps related to the dual need of foraging <strong>and</strong> mate<br />

location. Male massasaugas tracked for multiple years generally showed significant overlap in<br />

yearly movements, however, core areas of activity varied. However, King (1997) found<br />

significant differences between the sexes in several movement parameters <strong>and</strong> nongravid females<br />

had significantly smaller activity ranges than males. Several other studies of snakes have<br />

detected no differences between the sexes (e.g. Clark 1970, Plummer 1981, Michot 1981), while<br />

some studies find clear differences (Madsen 1984, Slip <strong>and</strong> Shine 1988), with the females<br />

generally possessing smaller activity ranges.<br />

Only one study (King 1997) has included data on movement from radio-marked neonate<br />

massasaugas. In his study, neonates made considerable movements, averaging similar distances<br />

per move <strong>and</strong> per day as nongravid females. Total distance moved per season <strong>and</strong> home range<br />

areas were similar to adult female massasaugas as well, although neonates were tracked for a<br />

8

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