Fig. 2 in A coalescent-based estimator of genetic drift, and acoustic divergence in the Pteronotus parnellii species complex
Fig. 2 Echolocation call frequency by island by sex and its relation to mass on the call frequency (F(1, 49) = 0.435, P value = 0.512). The body dimensions. a Boxplots of echolocation frequency (summarizing 95% HPD of population differences in means for body mass was 10 calls/individual). Bayesian 9...
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| creator | Dávalos, Liliana M. Lancaster, Winston C. Núñez-Novas, Miguel S. León, Yolanda M. Lei, Bonnie Flanders, Jon Russell, Amy L. |
| description | Fig. 2 Echolocation call frequency by island by sex and its relation to mass on the call frequency (F(1, 49) = 0.435, P value = 0.512). The body dimensions. a Boxplots of echolocation frequency (summarizing 95% HPD of population differences in means for body mass was 10 calls/individual). Bayesian 95% high-probability density (HPD) of 0.89–2.29 g. c Call frequency as a function of forearm length. Anathe difference in call frequency means between Puerto Rico and Hislyses of covariance support little influence of forearm length on the call paniola was 5.2–6.0 kHz. b Call frequency as a function of body mass. frequency (F(1, 52) = 2.851, P value = 0.097). The 95% HPD of Analyses of covariance support very different call frequency for island population differences in means for forearm lengths was −1.82, groups (F(1, 49) = 704.260, P value = 0.000), but no influence of body 0.422 mm |
| doi_str_mv | 10.5281/zenodo.7845699 |
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| title | Fig. 2 in A coalescent-based estimator of genetic drift, and acoustic divergence in the Pteronotus parnellii species complex |
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