ArticleJournal of neurophysiology2015
Automatic reconstruction of physiological gestures used in a model of birdsong production.
Article in Journal of neurophysiology, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 9 papers.
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9 citing papers in PubMed, 16 citations in OpenAlex.
- Timing of Speech in Brain and Glottis and the Feedback Delay Problem in Motor Control.The Journal of neuroscience : the official journal of the Society for Neuroscience · 2025Article
- Neurally driven synthesis of learned, complex vocalizations.Current biology : CB · 2021Article
- Gating related activity in a syringeal muscle allows the reconstruction of zebra finches songs.Chaos (Woodbury, N.Y.) · 2018Article
- Neural coding of sound envelope structure in songbirds.Journal of comparative physiology. A, Neuroethology, sensory, neural, and behavioral physiology · 2018Article
- From electromyographic activity to frequency modulation in zebra finch song.Journal of comparative physiology. A, Neuroethology, sensory, neural, and behavioral physiology · 2018Article
- Temperature manipulation of neuronal dynamics in a forebrain motor control nucleus.PLoS computational biology · 2017Article
- Rhythmic syllable-related activity in a songbird motor thalamic nucleus necessary for learned vocalizations.PloS one · 2017Article
- Population-Level Representation of a Temporal Sequence Underlying Song Production in the Zebra Finch.Neuron · 2016Article
- "Bird Song Metronomics": Isochronous Organization of Zebra Finch Song Rhythm.Frontiers in neuroscience · 2016Article
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Authors and funding
5 authors at 3 institutions in 2 countries.
Funding
Abstract
Highly coordinated learned behaviors are key to understanding neural processes integrating the body and the environment. Birdsong production is a widely studied example of such behavior in which numerous thoracic muscles control respiratory inspiration and expiration: the muscles of the syrinx control syringeal membrane tension, while upper vocal tract morphology controls resonances that modulate the vocal system output. All these muscles have to be coordinated in precise sequences to generate the elaborate vocalizations that characterize an individual's song. Previously we used a low-dimensional description of the biomechanics of birdsong production to investigate the associated neural codes, an approach that complements traditional spectrographic analysis. The prior study used algorithmic yet manual procedures to model singing behavior. In the present work, we present an automatic procedure to extract low-dimensional motor gestures that could predict vocal behavior. We recorded zebra finch songs and generated synthetic copies automatically, using a biomechanical model for the vocal apparatus and vocal tract. This dynamical model described song as a sequence of physiological parameters the birds control during singing. To validate this procedure, we recorded electrophysiological activity of the telencephalic nucleus HVC. HVC neurons were highly selective to the auditory presentation of the bird's own song (BOS) and gave similar selective responses to the automatically generated synthetic model of song (AUTO). Our results demonstrate meaningful dimensionality reduction in terms of physiological parameters that individual birds could actually control. Furthermore, this methodology can be extended to other vocal systems to study fine motor control.
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