Geographical variation in the echolocation calls of bent-winged bats, Miniopterus fuliginosus
•We studied geographical variation in echolocation calls of bent-winged bats (Miniopterus fuliginosus).•The peak frequency of seven colonies was similar, while only one colony was significantly higher than the others.•This variation patterns in echolocation calls may not be driven by genetic drift o...
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Published in | Zoology (Jena) Vol. 131; pp. 36 - 44 |
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Main Authors | , , , , , , |
Format | Journal Article |
Language | English |
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Elsevier GmbH
01.12.2018
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Abstract | •We studied geographical variation in echolocation calls of bent-winged bats (Miniopterus fuliginosus).•The peak frequency of seven colonies was similar, while only one colony was significantly higher than the others.•This variation patterns in echolocation calls may not be driven by genetic drift of M. fuliginosus.•The strong selective pressure induced by background noise may lead to acoustic divergence between JXT and the other colonies.
Evolutionary biologists had a long-standing interest in the evolutionary forces underlying geographical variation in the acoustic signals of animals. However, the evolutionary forces driving acoustic variation are still unclear. In this study, we quantified the geographical variation in the peak frequencies of echolocation calls in eight Miniopterus fuliginosus bat colonies, and assessed the forces that drive acoustic divergence. Our results demonstrated that seven of the colonies had very similar peak frequencies, while only one colony was significantly higher than the others. This similarity in echolocation call frequency among the seven colonies was likely due to frequent dispersal and migration, leading to male-mediated infiltration of nuclear genes. This infiltration enhances gene flow and weakens ecological selection, and also increases interactions in the presence of conspecifics. Significant correlations were not observed between acoustic distances and morphological distances, climatic differences, geographic distances or mtDNA genetic distances. However, variation in acoustic distances was significantly positive correlated with nDNA genetic distance, even after controlling for geographic distance. Interestingly, the relationship between call divergence and genetic distance was no longer significant after excluding the colony with the highest call frequency, which may be due to the minimal genetic distance among the other seven colonies. The highest frequencies of echolocation calls observed in the one colony may be shaped by selection pressure due to loud background noise in the area. Taken together, these results suggest that geographic divergence of echolocation calls may not be subject to genetic drift, but rather, that the strong selective pressure induced by background noise may lead to acoustic and genetic differentiation between JXT and the other colonies. |
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AbstractList | Evolutionary biologists had a long-standing interest in the evolutionary forces underlying geographical variation in the acoustic signals of animals. However, the evolutionary forces driving acoustic variation are still unclear. In this study, we quantified the geographical variation in the peak frequencies of echolocation calls in eight Miniopterus fuliginosus bat colonies, and assessed the forces that drive acoustic divergence. Our results demonstrated that seven of the colonies had very similar peak frequencies, while only one colony was significantly higher than the others. This similarity in echolocation call frequency among the seven colonies was likely due to frequent dispersal and migration, leading to male-mediated infiltration of nuclear genes. This infiltration enhances gene flow and weakens ecological selection, and also increases interactions in the presence of conspecifics. Significant correlations were not observed between acoustic distances and morphological distances, climatic differences, geographic distances or mtDNA genetic distances. However, variation in acoustic distances was significantly positive correlated with nDNA genetic distance, even after controlling for geographic distance. Interestingly, the relationship between call divergence and genetic distance was no longer significant after excluding the colony with the highest call frequency, which may be due to the minimal genetic distance among the other seven colonies. The highest frequencies of echolocation calls observed in the one colony may be shaped by selection pressure due to loud background noise in the area. Taken together, these results suggest that geographic divergence of echolocation calls may not be subject to genetic drift, but rather, that the strong selective pressure induced by background noise may lead to acoustic and genetic differentiation between JXT and the other colonies. •We studied geographical variation in echolocation calls of bent-winged bats (Miniopterus fuliginosus).•The peak frequency of seven colonies was similar, while only one colony was significantly higher than the others.•This variation patterns in echolocation calls may not be driven by genetic drift of M. fuliginosus.•The strong selective pressure induced by background noise may lead to acoustic divergence between JXT and the other colonies. Evolutionary biologists had a long-standing interest in the evolutionary forces underlying geographical variation in the acoustic signals of animals. However, the evolutionary forces driving acoustic variation are still unclear. In this study, we quantified the geographical variation in the peak frequencies of echolocation calls in eight Miniopterus fuliginosus bat colonies, and assessed the forces that drive acoustic divergence. Our results demonstrated that seven of the colonies had very similar peak frequencies, while only one colony was significantly higher than the others. This similarity in echolocation call frequency among the seven colonies was likely due to frequent dispersal and migration, leading to male-mediated infiltration of nuclear genes. This infiltration enhances gene flow and weakens ecological selection, and also increases interactions in the presence of conspecifics. Significant correlations were not observed between acoustic distances and morphological distances, climatic differences, geographic distances or mtDNA genetic distances. However, variation in acoustic distances was significantly positive correlated with nDNA genetic distance, even after controlling for geographic distance. Interestingly, the relationship between call divergence and genetic distance was no longer significant after excluding the colony with the highest call frequency, which may be due to the minimal genetic distance among the other seven colonies. The highest frequencies of echolocation calls observed in the one colony may be shaped by selection pressure due to loud background noise in the area. Taken together, these results suggest that geographic divergence of echolocation calls may not be subject to genetic drift, but rather, that the strong selective pressure induced by background noise may lead to acoustic and genetic differentiation between JXT and the other colonies. Evolutionary biologists had a long-standing interest in the evolutionary forces underlying geographical variation in the acoustic signals of animals. However, the evolutionary forces driving acoustic variation are still unclear. In this study, we quantified the geographical variation in the peak frequencies of echolocation calls in eight Miniopterus fuliginosus bat colonies, and assessed the forces that drive acoustic divergence. Our results demonstrated that seven of the colonies had very similar peak frequencies, while only one colony was significantly higher than the others. This similarity in echolocation call frequency among the seven colonies was likely due to frequent dispersal and migration, leading to male-mediated infiltration of nuclear genes. This infiltration enhances gene flow and weakens ecological selection, and also increases interactions in the presence of conspecifics. Significant correlations were not observed between acoustic distances and morphological distances, climatic differences, geographic distances or mtDNA genetic distances. However, variation in acoustic distances was significantly positive correlated with nDNA genetic distance, even after controlling for geographic distance. Interestingly, the relationship between call divergence and genetic distance was no longer significant after excluding the colony with the highest call frequency, which may be due to the minimal genetic distance among the other seven colonies. The highest frequencies of echolocation calls observed in the one colony may be shaped by selection pressure due to loud background noise in the area. Taken together, these results suggest that geographic divergence of echolocation calls may not be subject to genetic drift, but rather, that the strong selective pressure induced by background noise may lead to acoustic and genetic differentiation between JXT and the other colonies.Evolutionary biologists had a long-standing interest in the evolutionary forces underlying geographical variation in the acoustic signals of animals. However, the evolutionary forces driving acoustic variation are still unclear. In this study, we quantified the geographical variation in the peak frequencies of echolocation calls in eight Miniopterus fuliginosus bat colonies, and assessed the forces that drive acoustic divergence. Our results demonstrated that seven of the colonies had very similar peak frequencies, while only one colony was significantly higher than the others. This similarity in echolocation call frequency among the seven colonies was likely due to frequent dispersal and migration, leading to male-mediated infiltration of nuclear genes. This infiltration enhances gene flow and weakens ecological selection, and also increases interactions in the presence of conspecifics. Significant correlations were not observed between acoustic distances and morphological distances, climatic differences, geographic distances or mtDNA genetic distances. However, variation in acoustic distances was significantly positive correlated with nDNA genetic distance, even after controlling for geographic distance. Interestingly, the relationship between call divergence and genetic distance was no longer significant after excluding the colony with the highest call frequency, which may be due to the minimal genetic distance among the other seven colonies. The highest frequencies of echolocation calls observed in the one colony may be shaped by selection pressure due to loud background noise in the area. Taken together, these results suggest that geographic divergence of echolocation calls may not be subject to genetic drift, but rather, that the strong selective pressure induced by background noise may lead to acoustic and genetic differentiation between JXT and the other colonies. |
Author | Lin, Aiqing Lu, Guanjun Sun, Keping Jiang, Tinglei Liu, Sen Feng, Jiang Zhang, Chunmian |
Author_xml | – sequence: 1 givenname: Chunmian surname: Zhang fullname: Zhang, Chunmian organization: Jilin Provincial Key Laboratory of Animal Resource Conservation and Utilization, Northeast Normal University, Changchun, Jilin, PR China – sequence: 2 givenname: Tinglei surname: Jiang fullname: Jiang, Tinglei email: Jiangtl730@nenu.edu.cn organization: Jilin Provincial Key Laboratory of Animal Resource Conservation and Utilization, Northeast Normal University, Changchun, Jilin, PR China – sequence: 3 givenname: Guanjun surname: Lu fullname: Lu, Guanjun organization: College of Urban and Environment Science, Changchun Normal University, Changchun, 130032, PR China – sequence: 4 givenname: Aiqing surname: Lin fullname: Lin, Aiqing organization: Jilin Provincial Key Laboratory of Animal Resource Conservation and Utilization, Northeast Normal University, Changchun, Jilin, PR China – sequence: 5 givenname: Keping surname: Sun fullname: Sun, Keping organization: Jilin Provincial Key Laboratory of Animal Resource Conservation and Utilization, Northeast Normal University, Changchun, Jilin, PR China – sequence: 6 givenname: Sen surname: Liu fullname: Liu, Sen organization: Institute of Resources & Environment, Henan Polytechnic University, Jiaozuo, 454000, PR China – sequence: 7 givenname: Jiang surname: Feng fullname: Feng, Jiang email: fengj@nenu.edu.cn organization: Jilin Provincial Key Laboratory of Animal Resource Conservation and Utilization, Northeast Normal University, Changchun, Jilin, PR China |
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CitedBy_id | crossref_primary_10_1515_mammalia_2018_0197 crossref_primary_10_1007_s10340_023_01721_6 crossref_primary_10_1007_s13364_021_00570_x crossref_primary_10_1093_jisesa_iead048 crossref_primary_10_3161_15081109ACC2022_24_1_001 crossref_primary_10_1002_ece3_9126 crossref_primary_10_3389_fevo_2022_948324 crossref_primary_10_1016_j_anbehav_2020_10_003 |
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Keywords | echolocation call geographic variation peak frequency Miniopterus fuliginosus |
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Snippet | •We studied geographical variation in echolocation calls of bent-winged bats (Miniopterus fuliginosus).•The peak frequency of seven colonies was similar, while... Evolutionary biologists had a long-standing interest in the evolutionary forces underlying geographical variation in the acoustic signals of animals. However,... |
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SubjectTerms | Animal Distribution - physiology Animals Biological Evolution Chiroptera - physiology Echolocation - physiology echolocation call geographic variation Miniopterus fuliginosus peak frequency |
Title | Geographical variation in the echolocation calls of bent-winged bats, Miniopterus fuliginosus |
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