Acoustic Features of Rhesus Vocalizations and Their Representation in the Ventrolateral Prefrontal Cortex

2007 ◽  
Vol 97 (2) ◽  
pp. 1470-1484 ◽  
Author(s):  
Yale E. Cohen ◽  
Frédéric Theunissen ◽  
Brian E. Russ ◽  
Patrick Gill

Communication is one of the fundamental components of both human and nonhuman animal behavior. Auditory communication signals (i.e., vocalizations) are especially important in the socioecology of several species of nonhuman primates such as rhesus monkeys. In rhesus, the ventrolateral prefrontal cortex (vPFC) is thought to be part of a circuit involved in representing vocalizations and other auditory objects. To further our understanding of the role of the vPFC in processing vocalizations, we characterized the spectrotemporal features of rhesus vocalizations, compared these features with other classes of natural stimuli, and then related the rhesus-vocalization acoustic features to neural activity. We found that the range of these spectrotemporal features was similar to that found in other ensembles of natural stimuli, including human speech, and identified the subspace of these features that would be particularly informative to discriminate between different vocalizations. In a first neural study, however, we found that the tuning properties of vPFC neurons did not emphasize these particularly informative spectrotemporal features. In a second neural study, we found that a first-order linear model (the spectrotemporal receptive field) is not a good predictor of vPFC activity. The results of these two neural studies are consistent with the hypothesis that the vPFC is not involved in coding the first-order acoustic properties of a stimulus but is involved in processing the higher-order information needed to form representations of auditory objects.

PLoS ONE ◽  
2012 ◽  
Vol 7 (3) ◽  
pp. e34164 ◽  
Author(s):  
Béatrice Garcin ◽  
Emmanuelle Volle ◽  
Bruno Dubois ◽  
Richard Levy

2013 ◽  
Vol 280 (1754) ◽  
pp. 20122539 ◽  
Author(s):  
Pamela M. Fallow ◽  
Benjamin J. Pitcher ◽  
Robert D. Magrath

Vertebrates that eavesdrop on heterospecific alarm calls must distinguish alarms from sounds that can safely be ignored, but the mechanisms for identifying heterospecific alarm calls are poorly understood. While vertebrates learn to identify heterospecific alarms through experience, some can also respond to unfamiliar alarm calls that are acoustically similar to conspecific alarm calls. We used synthetic calls to test the role of specific acoustic properties in alarm call identification by superb fairy-wrens, Malurus cyaneus . Individuals fled more often in response to synthetic calls with peak frequencies closer to those of conspecific calls, even if other acoustic features were dissimilar to that of fairy-wren calls. Further, they then spent more time in cover following calls that had both peak frequencies and frequency modulation rates closer to natural fairy-wren means. Thus, fairy-wrens use similarity in specific acoustic properties to identify alarms and adjust a two-stage antipredator response. Our study reveals how birds respond to heterospecific alarm calls without experience, and, together with previous work using playback of natural calls, shows that both acoustic similarity and learning are important for interspecific eavesdropping. More generally, this study reconciles contrasting views on the importance of alarm signal structure and learning in recognition of heterospecific alarms.


2010 ◽  
Vol 113 (1) ◽  
pp. 28-38 ◽  
Author(s):  
Malathi Thothathiri ◽  
Myrna F. Schwartz ◽  
Sharon L. Thompson-Schill

2021 ◽  
Author(s):  
Cole Korponay

Habits allow environmental and interoceptive cues to trigger behavior in an automatized fashion, making them liable to deployment in inappropriate or outdated contexts. Over the long-term, repeated failure of a once adaptive habit to satisfy current goals produces extinction learning that suppresses the habit’s execution. Less attention has been afforded to the mechanisms underlying real-time habit suppression: the capacity to stop the execution of a cued habit that is goal-conflicting. Here, we first posit a model by which goal-relevant stimuli can 1) bring unfolding habits and their projected outcomes into awareness, 2) prompt evaluation of the habit outcome with respect to current goals, and 3) trigger cessation of the habit response if it is determined to be goal-conflicting. Second, we propose a modified stop-signal task to test this model of “goal-directed stopping of habit execution”. Finally, we marshal evidence indicating that the ventrolateral prefrontal cortex (vlPFC), situated at the nexus of salience detection, action-plan assessment, and motor inhibition networks, is uniquely positioned to coordinate the overriding of habitual behaviors in real time. In sum, this review presents a testable model and candidate neurobiological substrate for our capacity to “snap out of autopilot” and override goal-conflicting habits in real time.


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