Editorial Type:
Article Category: Research Article
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Online Publication Date: 14 Mar 2011

Clinal Variation in Calls of Native and Introduced Populations of Eleutherodactylus coqui

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Page Range: 18 – 28
DOI: 10.1643/CH-10-012
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We determined whether Eleutherodactylus coqui exhibits clinal variation in male advertisement call parameters across its native Puerto Rico and introduced range of Hawaii. In the laboratory, we determined whether clinal variation in call parameters were a result of body size or temperature. Calls correlate with elevation in both Puerto Rico and Hawaii in the following ways: negative for fundamental frequency of each call syllable (Co and Qui), positive with the duration of each call, negative with call rate (calls per minute), and no relationship with call intensity. In the laboratory, we found the negative relationship between elevation and call frequency was best explained by larger body sizes at higher elevations, and that the positive and negative relationships between elevation and call duration, and elevation and call rate, respectively, were best explained by lower temperatures at higher elevations. While frogs in Hawaii exhibited the same relationships between elevation and call parameters found in Puerto Rico, they exhibited less variation in call frequency with elevation because they had less variation in body size. Differences in call duration and rate between Hawaii and Puerto Rico reflected lower temperatures in Hawaii at similar elevations. While individual frogs are not louder in Hawaii, choruses may appear louder where densities are higher.

Copyright: 2011 by the American Society of Ichthyologists and Herpetologists
<bold>Fig. 1.</bold>
 
Fig. 1.

Map of study sites in (A) Hawaii and (B) Puerto Rico. Symbols follow Table 1.


<bold>Fig. 2.</bold>
 
Fig. 2.

Relationship between temperature and elevation in Hawaii and Puerto Rico. Data recorded in this study and mean annual temperatures (2001–2005) for ten NOAA stations in Puerto Rico (Adjuntas, Aibonito, Arecibo, Dorrado Airport, Guyama, Isabella, Juncos, Ponce, San Juan Airport, and Toro Negro Forest) and nine in Hawaii (Glenwood, Hilo airport, Kauamana, Kihalani, Kurtistown, Lalamilo Field, Opihihale, Puukohola, Heiau, and South Kona). Regression lines are based on NOAA data only.


<bold>Fig. 3.</bold>
 
Fig. 3.

The relationships between mean (± 1 SE) adult body size (snout–vent length, SVL) and (A) range and elevation and (B) site and elevation for male Eleutherodactylus coqui in Hawaii and Puerto Rico.


<bold>Fig. 4.</bold>
 
Fig. 4.

The relationships between mean (± 1 SE; A, B) Co and (C, D) Qui frequencies across (A, C) range and elevation and (B, D) site and elevation in Hawaii and Puerto Rico.


<bold>Fig. 5.</bold>
 
Fig. 5.

The relationships between mean (± 1 SE; A, B) call duration and (C, D) call rate across (A, C) range and elevation and (B, D) site and elevation in Hawaii and Puerto Rico.


<bold>Fig. 6.</bold>
 
Fig. 6.

The effect of (A, C, E, G) site and elevation and (B, D, F, H) temperature on mean (± 1 SE) Co and Qui frequencies, call rate, and call duration of Eleutherodactylus coqui from Hawaii (Hilo) and Puerto Rico (El Yunque and Rio Abajo) in the laboratory.


Contributor Notes

Associate Editor: M. J. Lannoo.

Department of Biology, Utah State University, Logan, Utah 84322-5305. Present address: Department of Biology, University of Kentucky, Lexington, Kentucky 40506-0225; E-mail: eric.oneill@uky.edu.
Department of Wildland Resources and the Ecology Center, Utah State University, Logan, Utah 84322-5230; E-mail: karen.beard@usu.edu. Send reprint requests to this address.
Received: 27 Jan 2010
Accepted: 17 Sept 2010
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