Echolocation-related reversal of information flow in a cortical vocalization network

The mammalian frontal and auditory cortices are important for vocal behavior. Here, using local-field potential recordings, we demonstrate that the timing and spatial patterns of oscillations in the fronto-auditory network of vocalizing bats ( Carollia perspicillata ) predict the purpose of vocaliza...

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Published inNature communications Vol. 13; no. 1; pp. 3642 - 15
Main Authors García-Rosales, Francisco, López-Jury, Luciana, González-Palomares, Eugenia, Wetekam, Johannes, Cabral-Calderín, Yuranny, Kiai, Ava, Kössl, Manfred, Hechavarría, Julio C.
Format Journal Article
LanguageEnglish
Published London Nature Publishing Group UK 25.06.2022
Nature Publishing Group
Nature Portfolio
Subjects
631/378/2619/2618
631/378/2629
631/378/3917
631/378/3920
Acoustics
Bats
Cortex (auditory)
Cortex (frontal)
Echolocation
Electrical stimuli
Entropy
Hearing
Humanities and Social Sciences
Information flow
Information transfer
Mammals
multidisciplinary
Oscillations
Science
Science (multidisciplinary)
Somatosensory cortex
Vocalization behavior
Online AccessGet full text
ISSN2041-1723
2041-1723
DOI10.1038/s41467-022-31230-6

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Abstract The mammalian frontal and auditory cortices are important for vocal behavior. Here, using local-field potential recordings, we demonstrate that the timing and spatial patterns of oscillations in the fronto-auditory network of vocalizing bats ( Carollia perspicillata ) predict the purpose of vocalization: echolocation or communication. Transfer entropy analyses revealed predominant top-down (frontal-to-auditory cortex) information flow during spontaneous activity and pre-vocal periods. The dynamics of information flow depend on the behavioral role of the vocalization and on the timing relative to vocal onset. We observed the emergence of predominant bottom-up (auditory-to-frontal) information transfer during the post-vocal period specific to echolocation pulse emission, leading to self-directed acoustic feedback. Electrical stimulation of frontal areas selectively enhanced responses to sounds in auditory cortex. These results reveal unique changes in information flow across sensory and frontal cortices, potentially driven by the purpose of the vocalization in a highly vocal mammalian model. How cortical areas interact during vocalization is not fully understood. Here the authors show that when bats vocalize, the behavioral function of emitted sounds determines the direction of information flow between frontal and auditory cortices.
AbstractList The mammalian frontal and auditory cortices are important for vocal behavior. Here, using local-field potential recordings, we demonstrate that the timing and spatial patterns of oscillations in the fronto-auditory network of vocalizing bats ( Carollia perspicillata ) predict the purpose of vocalization: echolocation or communication. Transfer entropy analyses revealed predominant top-down (frontal-to-auditory cortex) information flow during spontaneous activity and pre-vocal periods. The dynamics of information flow depend on the behavioral role of the vocalization and on the timing relative to vocal onset. We observed the emergence of predominant bottom-up (auditory-to-frontal) information transfer during the post-vocal period specific to echolocation pulse emission, leading to self-directed acoustic feedback. Electrical stimulation of frontal areas selectively enhanced responses to sounds in auditory cortex. These results reveal unique changes in information flow across sensory and frontal cortices, potentially driven by the purpose of the vocalization in a highly vocal mammalian model. How cortical areas interact during vocalization is not fully understood. Here the authors show that when bats vocalize, the behavioral function of emitted sounds determines the direction of information flow between frontal and auditory cortices.
The mammalian frontal and auditory cortices are important for vocal behavior. Here, using local-field potential recordings, we demonstrate that the timing and spatial patterns of oscillations in the fronto-auditory network of vocalizing bats (Carollia perspicillata) predict the purpose of vocalization: echolocation or communication. Transfer entropy analyses revealed predominant top-down (frontal-to-auditory cortex) information flow during spontaneous activity and pre-vocal periods. The dynamics of information flow depend on the behavioral role of the vocalization and on the timing relative to vocal onset. We observed the emergence of predominant bottom-up (auditory-to-frontal) information transfer during the post-vocal period specific to echolocation pulse emission, leading to self-directed acoustic feedback. Electrical stimulation of frontal areas selectively enhanced responses to sounds in auditory cortex. These results reveal unique changes in information flow across sensory and frontal cortices, potentially driven by the purpose of the vocalization in a highly vocal mammalian model.How cortical areas interact during vocalization is not fully understood. Here the authors show that when bats vocalize, the behavioral function of emitted sounds determines the direction of information flow between frontal and auditory cortices.
The mammalian frontal and auditory cortices are important for vocal behavior. Here, using local-field potential recordings, we demonstrate that the timing and spatial patterns of oscillations in the fronto-auditory network of vocalizing bats ( Carollia perspicillata ) predict the purpose of vocalization: echolocation or communication. Transfer entropy analyses revealed predominant top-down (frontal-to-auditory cortex) information flow during spontaneous activity and pre-vocal periods. The dynamics of information flow depend on the behavioral role of the vocalization and on the timing relative to vocal onset. We observed the emergence of predominant bottom-up (auditory-to-frontal) information transfer during the post-vocal period specific to echolocation pulse emission, leading to self-directed acoustic feedback. Electrical stimulation of frontal areas selectively enhanced responses to sounds in auditory cortex. These results reveal unique changes in information flow across sensory and frontal cortices, potentially driven by the purpose of the vocalization in a highly vocal mammalian model.
How cortical areas interact during vocalization is not fully understood. Here the authors show that when bats vocalize, the behavioral function of emitted sounds determines the direction of information flow between frontal and auditory cortices.
The mammalian frontal and auditory cortices are important for vocal behavior. Here, using local-field potential recordings, we demonstrate that the timing and spatial patterns of oscillations in the fronto-auditory network of vocalizing bats (Carollia perspicillata) predict the purpose of vocalization: echolocation or communication. Transfer entropy analyses revealed predominant top-down (frontal-to-auditory cortex) information flow during spontaneous activity and pre-vocal periods. The dynamics of information flow depend on the behavioral role of the vocalization and on the timing relative to vocal onset. We observed the emergence of predominant bottom-up (auditory-to-frontal) information transfer during the post-vocal period specific to echolocation pulse emission, leading to self-directed acoustic feedback. Electrical stimulation of frontal areas selectively enhanced responses to sounds in auditory cortex. These results reveal unique changes in information flow across sensory and frontal cortices, potentially driven by the purpose of the vocalization in a highly vocal mammalian model.The mammalian frontal and auditory cortices are important for vocal behavior. Here, using local-field potential recordings, we demonstrate that the timing and spatial patterns of oscillations in the fronto-auditory network of vocalizing bats (Carollia perspicillata) predict the purpose of vocalization: echolocation or communication. Transfer entropy analyses revealed predominant top-down (frontal-to-auditory cortex) information flow during spontaneous activity and pre-vocal periods. The dynamics of information flow depend on the behavioral role of the vocalization and on the timing relative to vocal onset. We observed the emergence of predominant bottom-up (auditory-to-frontal) information transfer during the post-vocal period specific to echolocation pulse emission, leading to self-directed acoustic feedback. Electrical stimulation of frontal areas selectively enhanced responses to sounds in auditory cortex. These results reveal unique changes in information flow across sensory and frontal cortices, potentially driven by the purpose of the vocalization in a highly vocal mammalian model.
ArticleNumber 3642
Author González-Palomares, Eugenia
Kössl, Manfred
López-Jury, Luciana
Hechavarría, Julio C.
Wetekam, Johannes
García-Rosales, Francisco
Cabral-Calderín, Yuranny
Kiai, Ava
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  publication-title: Behaviour
  doi: 10.1163/1568539X-00003171
– volume: 32
  start-page: 10737
  year: 2012
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  publication-title: J. Neurosci.
  doi: 10.1523/JNEUROSCI.3448-11.2012
– volume: 178
  start-page: 413
  year: 2019
  ident: 31230_CR51
  publication-title: Cell
  doi: 10.1016/j.cell.2019.05.023
– volume: 76
  start-page: 695
  year: 2012
  ident: 31230_CR74
  publication-title: Neuron
  doi: 10.1016/j.neuron.2012.10.038
SSID ssj0000391844
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Snippet The mammalian frontal and auditory cortices are important for vocal behavior. Here, using local-field potential recordings, we demonstrate that the timing and...
How cortical areas interact during vocalization is not fully understood. Here the authors show that when bats vocalize, the behavioral function of emitted...
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SubjectTerms 631/378/2619/2618
631/378/2629
631/378/3917
631/378/3920
Acoustics
Bats
Cortex (auditory)
Cortex (frontal)
Echolocation
Electrical stimuli
Entropy
Hearing
Humanities and Social Sciences
Information flow
Information transfer
Mammals
multidisciplinary
Oscillations
Science
Science (multidisciplinary)
Somatosensory cortex
Vocalization behavior
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Title Echolocation-related reversal of information flow in a cortical vocalization network
URI https://link.springer.com/article/10.1038/s41467-022-31230-6
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https://pubmed.ncbi.nlm.nih.gov/PMC9233670
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Volume 13
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