Betsie Rothermel

Dr. Betsie Rothermel

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Research Focus & Metrics

Academic Career Length

26Years (2001-Present)

(Calculated once Scilit publication data is synced: current year − year of first publication + 1)

Representative Publications

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30 June 2006 in Conservation Biology
Verified
Journal Article
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JGJ. Whitfield Gibbons
J. Whitfield Gibbons
CWChristopher T. Winne
Christopher T. Winne
DSDavid E. Scott
David E. Scott
JWJohn D. Willson
John D. Willson
XGXavier Glaudas
Xavier Glaudas
BRBetsie Rothermel
Betsie Rothermel

1 November 2009 in BioScience
Verified
Journal Article
Closed access
RSRaymond D. Semlitsch
Raymond D. Semlitsch
BTBrian D. Todd
Brian D. Todd
SBSean M. Blomquist
Sean M. Blomquist
ACAram J. K. Calhoun
Aram J. K. Calhoun
JGJ. Whitfield Gibbons
J. Whitfield Gibbons
BRBetsie Rothermel
Betsie Rothermel

20 April 2015 in Molecular Ecology
Verified
Journal Article
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MYMichael L. Yuan
Michael L. Yuan
SDSamantha H. Dean
Samantha H. Dean
ALAna V. Longo
Ana V. Longo
BRBetsie Rothermel
Betsie Rothermel
TTTracey D. Tuberville
Tracey D. Tuberville
KZKelly R. Zamudio
Kelly R. Zamudio

1 October 2004 in Ecological Applications
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Journal Article
Open access
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BRBetsie Rothermel
Betsie Rothermel
The persistence of pond‐breeding amphibians in highly fragmented landscapes may be constrained by the need for connectivity between aquatic breeding sites and suitable terrestrial habitat, an example of landscape complementation. Although migratory ability determines the spatial scale at which landscape complementation operates, the factors influencing migratory success of amphibians, especially of juveniles, are poorly understood. This study is the first to investigate whether juvenile amphibians possess any innate, long‐distance orientation mechanisms that might improve their chances of locating suitable terrestrial habitat. I conducted experimental releases of spotted salamanders (Ambystoma maculatum) and American toads (Bufo americanus) from 18 artificial pools in replicate pastures at distances of 5–50 m from the nearest forest edges. Using circular drift fences with pitfall traps, I captured, individually marked, and released metamorphosed salamanders (n = 323) and toads (n = 203) leaving each pool. Salamanders exhibited nonrandom orientation at nine pools, but at only one was the mean movement direction consistent with the direction to the nearest forest edge. Emigrating salamanders probably responded to microtopographic or other distinct features of each pool, rather than to distant cues. Migratory success was determined by recaptures of marked juveniles at drift fences along the forest edges. I used logistic regression to model probability of recapture and evaluated alternative models using an information‐theoretic approach. Migratory success of both species was primarily a function of distance to nearest forest. Of salamanders and toads released from 50‐m pools, <15% reached the forest, suggesting that few juvenile amphibians would be able to migrate greater distances across pastures. Breeding sites lacking connectivity to suitable terrestrial habitat may be population sinks due to high mortality of juveniles during emigration. Additional research is needed to determine appropriate threshold distances between breeding sites and terrestrial habitat, as well as the potential effectiveness of movement corridors for migrating amphibians.