Abstract:The creation of novel communicative acts is an essential element of human language. Although some research suggests the presence of this ability in great apes, this claim remains controversial. Here, we use orang-utans (Pongo spp.) to systematically assess the effect of the wild-captive contrast on the repertoire size of communicative acts. We find that individual communicative repertoires are significantly larger in captive compared to wild settings, irrespective of species, age-sex class or sampling effort. … Show more
“…Orang-utans showed little variability in the types of gestures used within age classes, with mother-infant dyads using the same travel-initiation gestures as other members of their age group (but different from other age groups; Cartmill & Byrne 2010 ), while chimpanzee mothers living in the same community used different sets of gestures to initiate travel with their infants (Fröhlich et al 2016b ). However, here orang-utan data were limited to small numbers of captive individuals, and in other settings captivity appeared to increase diversity of gesture use in orang-utans (Fröhlich et al 2021 ).…”
Section: Individual Variation In Gesture Usementioning
confidence: 90%
“…The majority of these apparently novel “inventions” were gesture types typical in other ape species (e.g., cf. Fröhlich et al 2021 with Byrne et al 2017 ), suggesting that while immediate socio-ecology shapes local repertoires in particular ways, apes retain access to shared ape-typical sets of available signals.…”
Section: (Sub)species Variation In Gesture Usementioning
confidence: 99%
“…Orang-utans were found to be highly responsive in their gesturing, typically responding before their partner’s gestures were completed, perhaps as a result of their familiarity (Knox et al 2019 ). Interestingly, in the unusual socio-ecological contexts of captivity where orang-utans are kept in atypically large social groups and experience a more terrestrial lifestyle, their repertoires of regularly used signals were larger (Fröhlich et al 2021 ). The majority of these apparently novel “inventions” were gesture types typical in other ape species (e.g., cf.…”
Section: (Sub)species Variation In Gesture Usementioning
Exaggerated anticipatory anxiety is common in social anxiety disorder (SAD).
Neuroimaging studies have revealed altered neural activity in response to social stimuli in SAD, but fewer studies have examined neural activity during anticipation of feared social stimuli in SAD.
The current study examined the time course and magnitude of activity in threat processing brain regions during speech anticipation in socially anxious individuals and healthy controls (HC).
Method Participants (SAD n = 58; HC n = 16) underwent functional magnetic resonance imaging (fMRI) during which they completed a 90s control anticipation task and 90s speech anticipation task.
Exaggerated anticipatory anxiety is common in social anxiety disorder (SAD).
Neuroimaging studies have revealed altered neural activity in response to social stimuli in SAD, but fewer studies have examined neural activity during anticipation of feared social stimuli in SAD.
The current study examined the time course and magnitude of activity in threat processing brain regions during speech anticipation in socially anxious individuals and healthy controls (HC).
Method Participants (SAD n = 58; HC n = 16) underwent functional magnetic resonance imaging (fMRI) during which they completed a 90s control anticipation task and 90s speech anticipation task.
“…Orang-utans showed little variability in the types of gestures used within age classes, with mother-infant dyads using the same travel-initiation gestures as other members of their age group (but different from other age groups; Cartmill & Byrne 2010 ), while chimpanzee mothers living in the same community used different sets of gestures to initiate travel with their infants (Fröhlich et al 2016b ). However, here orang-utan data were limited to small numbers of captive individuals, and in other settings captivity appeared to increase diversity of gesture use in orang-utans (Fröhlich et al 2021 ).…”
Section: Individual Variation In Gesture Usementioning
confidence: 90%
“…The majority of these apparently novel “inventions” were gesture types typical in other ape species (e.g., cf. Fröhlich et al 2021 with Byrne et al 2017 ), suggesting that while immediate socio-ecology shapes local repertoires in particular ways, apes retain access to shared ape-typical sets of available signals.…”
Section: (Sub)species Variation In Gesture Usementioning
confidence: 99%
“…Orang-utans were found to be highly responsive in their gesturing, typically responding before their partner’s gestures were completed, perhaps as a result of their familiarity (Knox et al 2019 ). Interestingly, in the unusual socio-ecological contexts of captivity where orang-utans are kept in atypically large social groups and experience a more terrestrial lifestyle, their repertoires of regularly used signals were larger (Fröhlich et al 2021 ). The majority of these apparently novel “inventions” were gesture types typical in other ape species (e.g., cf.…”
Section: (Sub)species Variation In Gesture Usementioning
Exaggerated anticipatory anxiety is common in social anxiety disorder (SAD).
Neuroimaging studies have revealed altered neural activity in response to social stimuli in SAD, but fewer studies have examined neural activity during anticipation of feared social stimuli in SAD.
The current study examined the time course and magnitude of activity in threat processing brain regions during speech anticipation in socially anxious individuals and healthy controls (HC).
Method Participants (SAD n = 58; HC n = 16) underwent functional magnetic resonance imaging (fMRI) during which they completed a 90s control anticipation task and 90s speech anticipation task.
Exaggerated anticipatory anxiety is common in social anxiety disorder (SAD).
Neuroimaging studies have revealed altered neural activity in response to social stimuli in SAD, but fewer studies have examined neural activity during anticipation of feared social stimuli in SAD.
The current study examined the time course and magnitude of activity in threat processing brain regions during speech anticipation in socially anxious individuals and healthy controls (HC).
Method Participants (SAD n = 58; HC n = 16) underwent functional magnetic resonance imaging (fMRI) during which they completed a 90s control anticipation task and 90s speech anticipation task.
Exaggerated anticipatory anxiety is common in social anxiety disorder (SAD).
Neuroimaging studies have revealed altered neural activity in response to social stimuli in SAD, but fewer studies have examined neural activity during anticipation of feared social stimuli in SAD.
The current study examined the time course and magnitude of activity in threat processing brain regions during speech anticipation in socially anxious individuals and healthy controls (HC).
Method Participants (SAD n = 58; HC n = 16) underwent functional magnetic resonance imaging (fMRI) during which they completed a 90s control anticipation task and 90s speech anticipation task.
Exaggerated anticipatory anxiety is common in social anxiety disorder (SAD).
Neuroimaging studies have revealed altered neural activity in response to social stimuli in SAD, but fewer studies have examined neural activity during anticipation of feared social stimuli in SAD.
The current study examined the time course and magnitude of activity in threat processing brain regions during speech anticipation in socially anxious individuals and healthy controls (HC).
Method Participants (SAD n = 58; HC n = 16) underwent functional magnetic resonance imaging (fMRI) during which they completed a 90s control anticipation task and 90s speech anticipation task.
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