TY - JOUR
T1 - The origins of acoustic communication in vertebrates
AU - Chen, Zhuo
AU - Wiens, John J.
N1 - Funding Information:
We thank C. Román-Palacios, E. Miller, Y. Qu, and P. Li for help and A. Li, J. Tian, X. Zhai, X. Hong, and Y. Zhu for providing the animal images used in Fig. 1. Z.C. was funded by the National Natural Science Foundation of China (31601848, U1404306, 31572245, and 31872220), International Postdoctoral Exchange Fellowship Program from China Postdoctoral Council (20170028), China Postdoctoral Science Foundation (2016M600580), and Excellent Young Scholars Fund of HNNU (YQ201706). J.J.W. acknowledges support of U.S. National Science Foundation grant DEB 1655690.
Publisher Copyright:
© 2020, The Author(s).
PY - 2020/12/1
Y1 - 2020/12/1
N2 - Acoustic communication is crucial to humans and many other tetrapods, including birds, frogs, crocodilians, and mammals. However, large-scale patterns in its evolution are largely unstudied. Here, we address several fundamental questions about the origins of acoustic communication in terrestrial vertebrates (tetrapods), using phylogenetic methods. We show that origins of acoustic communication are significantly associated with nocturnal activity. We find that acoustic communication does not increase diversification rates, a surprising result given the many speciation-focused studies of frog calls and bird songs. We also demonstrate that the presence of acoustic communication is strongly conserved over time. Finally, we find that acoustic communication evolved independently in most major tetrapod groups, often with remarkably ancient origins (~100–200 million years ago). Overall, we show that the role of ecology in shaping signal evolution applies to surprisingly deep timescales, whereas the role of signal evolution in diversification may not.
AB - Acoustic communication is crucial to humans and many other tetrapods, including birds, frogs, crocodilians, and mammals. However, large-scale patterns in its evolution are largely unstudied. Here, we address several fundamental questions about the origins of acoustic communication in terrestrial vertebrates (tetrapods), using phylogenetic methods. We show that origins of acoustic communication are significantly associated with nocturnal activity. We find that acoustic communication does not increase diversification rates, a surprising result given the many speciation-focused studies of frog calls and bird songs. We also demonstrate that the presence of acoustic communication is strongly conserved over time. Finally, we find that acoustic communication evolved independently in most major tetrapod groups, often with remarkably ancient origins (~100–200 million years ago). Overall, we show that the role of ecology in shaping signal evolution applies to surprisingly deep timescales, whereas the role of signal evolution in diversification may not.
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U2 - 10.1038/s41467-020-14356-3
DO - 10.1038/s41467-020-14356-3
M3 - Article
C2 - 31953401
AN - SCOPUS:85077985166
VL - 11
JO - Nature Communications
JF - Nature Communications
SN - 2041-1723
IS - 1
M1 - 369
ER -