Evidence map›Paper›PMID 41162946›Full record

ArticleBMC biology2025

Prey evasiveness and masking noise jointly promote the ultrahigh call rate in echolocating bats.

Nina Ma, Hangjing Xia, Huijuan Zheng, Jinhong Luo

Abstract read
In one paragraph

Article in BMC biology, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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0citing papers in PubMed
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1 · What the graph read from it

What it found

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2 · The registry

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3 · Its place in the literature

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4 · The record

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PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

4 authors.

Nina MaKey Laboratory of Pesticide and Chemical Biology of Ministry of Education, Hubei Key Laboratory of Genetic Regulation and Integrative Biology, School of Life Sciences, Central China Normal University, Wuhan, 430079, China.
Hangjing XiaKey Laboratory of Pesticide and Chemical Biology of Ministry of Education, Hubei Key Laboratory of Genetic Regulation and Integrative Biology, School of Life Sciences, Central China Normal University, Wuhan, 430079, China.
Huijuan ZhengKey Laboratory of Pesticide and Chemical Biology of Ministry of Education, Hubei Key Laboratory of Genetic Regulation and Integrative Biology, School of Life Sciences, Central China Normal University, Wuhan, 430079, China.
Jinhong LuoKey Laboratory of Pesticide and Chemical Biology of Ministry of Education, Hubei Key Laboratory of Genetic Regulation and Integrative Biology, School of Life Sciences, Central China Normal University, Wuhan, 430079, China. jluo@ccnu.edu.cn.

Funding

National Natural Science Foundation of China 32270535
6 · The paper itself

Abstract

backgroundAmong mammals, only bats and toothed whales are known to produce > 160 calls per second, which occurs shortly before these echolocators capture their prey. This high call rate phase, dubbed terminal buzz, is powered by rare superfast muscles. The enigmatic terminal buzz of bats is hypothesized to have evolved in response to the challenges of capturing flying insects. However, it remains unclear why some bats produce a full terminal buzz sequence when capturing stationary, inescapable prey, such as insect larvae suspended in the air. Here, we recorded bats performing foraging and orientation tasks in a laboratory setting, both with and without acoustic masking noise.

resultsWe discovered that masking noise selectively enhanced the call rate of Pratt's roundleaf bats during foraging, but not during landing tasks. We found that the prevalence and elaboration of terminal buzz in these bats were determined by prey evasiveness, with the most frequent and elaborated terminal buzz occurring for bats capturing flying insects. Unlike other reported aerial hawking bats, the Pratt's roundleaf bats did not exhibit a terminal buzz when capturing stationary, inescapable insect larvae. Surprisingly, the absence of terminal buzz can be instantly restored by exposing bats to masking noise. In contrast, masking noise had only a minimal effect on the buzz-like calls produced during a landing task.

conclusionsWe posit that prey evasiveness and masking noise, two primary challenges faced by both echolocating bats and toothed whales, jointly drove the evolution of the ultrahigh call rate of terminal buzz.

Indexed as

ChiropteraEcholocationNoisePredatory BehaviorVocalization, AnimalAnimalsEcholocationForaging behaviorMasking noiseSuperfast muscleTerminal buzz

Identifiers

PMID41162946
PMCPMC12574097

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LicenceCC BY-NC-ND
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Registered trials

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.