Cargando…

Insectivorous bats integrate social information about species identity, conspecific activity and prey abundance to estimate cost–benefit ratio of interactions

1. Animals can use inadvertent social information to improve fitness‐relevant decisions, for instance about where to forage or with whom to interact. Since bats emit high‐amplitude species‐specific echolocation calls when flying, they provide a constant flow of inadvertent social information to othe...

Descripción completa

Detalles Bibliográficos
Autores principales: Lewanzik, Daniel, Sundaramurthy, Arun K., Goerlitz, Holger R.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6849779/
https://www.ncbi.nlm.nih.gov/pubmed/30945281
http://dx.doi.org/10.1111/1365-2656.12989
_version_ 1783469276563243008
author Lewanzik, Daniel
Sundaramurthy, Arun K.
Goerlitz, Holger R.
author_facet Lewanzik, Daniel
Sundaramurthy, Arun K.
Goerlitz, Holger R.
author_sort Lewanzik, Daniel
collection PubMed
description 1. Animals can use inadvertent social information to improve fitness‐relevant decisions, for instance about where to forage or with whom to interact. Since bats emit high‐amplitude species‐specific echolocation calls when flying, they provide a constant flow of inadvertent social information to others who can decode that acoustic information. Of particular interest is the rate of feeding buzzes—characteristic call sequences preceding any prey capture—which correlates with insect abundance. 2. Previous studies investigating eavesdropping in bats yielded very different and in part contradictory results likely because they commonly focused on single species only, differed substantially in playback buzz rate and did usually not account for (baseline) conspecific activity. Our goal was to overcome these limitations and systematically test which inadvertent social information bats integrate when eavesdropping on others and how this integration affects space use and both intra‐ and interspecific interactions, respectively. 3. We used a community‐wide approach and investigated the effects of a broad range of playback feeding buzz rates and conspecific activity on eavesdropping responses in 24 bat species combinations in the wild. 4. For the first time, we reveal that finely graded and density‐dependent eavesdropping responses are not limited to particular foraging styles or call types, but instead are ubiquitous among insectivorous bats. All bats integrated social information about calling species identity, prey abundance and conspecific activity to estimate the cost–benefit ratio of prospective interactions, yet in a species‐specific manner. The effect of buzz rate was multifaceted, as bats responded differently to different buzz rates, and responses were additionally modulated by heterospecific recognition. Conspecific activity, in contrast, had a negative effect on the eavesdropping responses of all bats. 5. These findings can explain the inconsistent results of previous studies and advance our understanding of the complex nature of conspecific and heterospecific interactions within bat communities. A comprehensive understanding of how bats incorporate social information into their decision‐making will help researchers to explain species distribution patterns and eventually to unravel mechanisms of species coexistence.
format Online
Article
Text
id pubmed-6849779
institution National Center for Biotechnology Information
language English
publishDate 2019
publisher John Wiley and Sons Inc.
record_format MEDLINE/PubMed
spelling pubmed-68497792019-11-15 Insectivorous bats integrate social information about species identity, conspecific activity and prey abundance to estimate cost–benefit ratio of interactions Lewanzik, Daniel Sundaramurthy, Arun K. Goerlitz, Holger R. J Anim Ecol Behavioural Ecology 1. Animals can use inadvertent social information to improve fitness‐relevant decisions, for instance about where to forage or with whom to interact. Since bats emit high‐amplitude species‐specific echolocation calls when flying, they provide a constant flow of inadvertent social information to others who can decode that acoustic information. Of particular interest is the rate of feeding buzzes—characteristic call sequences preceding any prey capture—which correlates with insect abundance. 2. Previous studies investigating eavesdropping in bats yielded very different and in part contradictory results likely because they commonly focused on single species only, differed substantially in playback buzz rate and did usually not account for (baseline) conspecific activity. Our goal was to overcome these limitations and systematically test which inadvertent social information bats integrate when eavesdropping on others and how this integration affects space use and both intra‐ and interspecific interactions, respectively. 3. We used a community‐wide approach and investigated the effects of a broad range of playback feeding buzz rates and conspecific activity on eavesdropping responses in 24 bat species combinations in the wild. 4. For the first time, we reveal that finely graded and density‐dependent eavesdropping responses are not limited to particular foraging styles or call types, but instead are ubiquitous among insectivorous bats. All bats integrated social information about calling species identity, prey abundance and conspecific activity to estimate the cost–benefit ratio of prospective interactions, yet in a species‐specific manner. The effect of buzz rate was multifaceted, as bats responded differently to different buzz rates, and responses were additionally modulated by heterospecific recognition. Conspecific activity, in contrast, had a negative effect on the eavesdropping responses of all bats. 5. These findings can explain the inconsistent results of previous studies and advance our understanding of the complex nature of conspecific and heterospecific interactions within bat communities. A comprehensive understanding of how bats incorporate social information into their decision‐making will help researchers to explain species distribution patterns and eventually to unravel mechanisms of species coexistence. John Wiley and Sons Inc. 2019-04-22 2019-10 /pmc/articles/PMC6849779/ /pubmed/30945281 http://dx.doi.org/10.1111/1365-2656.12989 Text en © 2019 The Authors. Journal of Animal Ecology published by John Wiley & Sons Ltd on behalf of British Ecological Society. This is an open access article under the terms of the http://creativecommons.org/licenses/by/4.0/ License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited.
spellingShingle Behavioural Ecology
Lewanzik, Daniel
Sundaramurthy, Arun K.
Goerlitz, Holger R.
Insectivorous bats integrate social information about species identity, conspecific activity and prey abundance to estimate cost–benefit ratio of interactions
title Insectivorous bats integrate social information about species identity, conspecific activity and prey abundance to estimate cost–benefit ratio of interactions
title_full Insectivorous bats integrate social information about species identity, conspecific activity and prey abundance to estimate cost–benefit ratio of interactions
title_fullStr Insectivorous bats integrate social information about species identity, conspecific activity and prey abundance to estimate cost–benefit ratio of interactions
title_full_unstemmed Insectivorous bats integrate social information about species identity, conspecific activity and prey abundance to estimate cost–benefit ratio of interactions
title_short Insectivorous bats integrate social information about species identity, conspecific activity and prey abundance to estimate cost–benefit ratio of interactions
title_sort insectivorous bats integrate social information about species identity, conspecific activity and prey abundance to estimate cost–benefit ratio of interactions
topic Behavioural Ecology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6849779/
https://www.ncbi.nlm.nih.gov/pubmed/30945281
http://dx.doi.org/10.1111/1365-2656.12989
work_keys_str_mv AT lewanzikdaniel insectivorousbatsintegratesocialinformationaboutspeciesidentityconspecificactivityandpreyabundancetoestimatecostbenefitratioofinteractions
AT sundaramurthyarunk insectivorousbatsintegratesocialinformationaboutspeciesidentityconspecificactivityandpreyabundancetoestimatecostbenefitratioofinteractions
AT goerlitzholgerr insectivorousbatsintegratesocialinformationaboutspeciesidentityconspecificactivityandpreyabundancetoestimatecostbenefitratioofinteractions