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Neural dynamics and acoustic adaptations during the Lombard effect: evidence from EEG and dynamic causal modeling
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  • Open access
  • Published: 24 April 2026

Neural dynamics and acoustic adaptations during the Lombard effect: evidence from EEG and dynamic causal modeling

  • Lucía Z-Rivera1,2,3 na1,
  • Christian Castro4,5 na1,
  • Jhosmary Cuadros1,6,7,
  • Juan P. Cortés1,
  • Alejandro Weinstein1,8,
  • Víctor M. Espinoza9,
  • Pavel Prado10 &
  • …
  • Matías Zañartu1,8 

Scientific Reports (2026) Cite this article

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  • Neuroscience
  • Physiology

Abstract

The Lombard Effect (LE) is a vocal adaptation in which speakers involuntarily increase their vocal effort to preserve intelligibility in high-noise environments. This study explores acoustic and neurophysiological mechanisms that support LE in individuals with typical voices. Twenty-one participants produced 80 syllables under three conditions: Baseline (quiet), Lombard (noise at 80 dB SPL), and Recovery (quiet after five minutes of rest). Acoustic signals and electroencephalography (EEG) data were recorded synchronously, focusing on sound pressure level (SPL), H1–H2 (the difference in amplitude between the first and second harmonics), Cepstral Peak Prominence (CPP), Event-Related Potentials (ERPs) time-locked to the onset of self-produced vocalizations, and effective connectivity through Dynamic Causal Modeling (DCM). Results showed a significant increase in SPL during the Lombard condition compared to Baseline and Recovery. In this condition, H1–H2 values decreased and CPP increased, with no differences between Baseline and Recovery across the three acoustic measures. ERP analysis revealed a higher N1-P2 amplitude in the Lombard condition, associated with increased activations in frontal, limbic, and temporal brain regions. Bayesian model selection within the DCM framework indicated that the best-fitting model explaining the ERP data was a forward network from the primary auditory cortex (A1) to the temporal pole (TPO), inferior frontal gyrus (IFG), and parahippocampal gyrus (PHG), with modulatory connections highlighting feedback mechanisms. Within this network, the IFG and PHG seem to play a central role in error detection and feedback modulation, while the TPO supports auditory processing, together supporting the neural adjustments that sustain intelligible speech in noise. These results provide new insights into the cortical network underlying LE, emphasizing the adaptive mechanisms in speech production under noisy conditions.

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Funding

This research was supported in part by Agencia Nacional de Investigación y Desarrollo (ANID), Chile, through grants FONDECYT 1230828 (M.Z), CIA250006 (MZ and AW), ANILLO ANID/ACT210053 (A.W), FONDECYT 1241142 (V.E), FONDECYT 11251641 (J.C), FONDECYT 1260530 (P.P), and Fulbright-ANID BIO Scholarship (2021, Folio No 56210070) (L.Z-R). This research was also supported by the National Institutes of Health (NIH) National Institute on Deafness and Other Communication Disorders, United States grant P50 DC015446. The content is solely the responsibility of the authors and does not necessarily represent the official views of the NIH.

Author information

Author notes
  1. Lucia Z-Rivera and Christian Castro contributed equally to this work.

Authors and Affiliations

  1. Advanced Center for Electrical and Electronic Engineering, Universidad Técnica Federico Santa María, Valparaíso, Chile

    Lucía Z-Rivera, Jhosmary Cuadros, Juan P. Cortés, Alejandro Weinstein & Matías Zañartu

  2. Neuroscience and Cognitive Science Program, University of Maryland, College Park, MD, USA

    Lucía Z-Rivera

  3. Department of Human Development and Quantitative Methodology, University of Maryland, College Park, MD, USA

    Lucía Z-Rivera

  4. Exercise and Rehabilitation Sciences Institute, School of Speech Therapy, Faculty of Rehabilitation Sciences, Universidad Andres Bello, Santiago, 7591538, Chile

    Christian Castro

  5. Ph.D. Program in Health Science and Engineering Universidad de Valparaíso, Valparaíso, Chile

    Christian Castro

  6. Latin American Brain Health Institute (BrainLat), Universidad Adolfo Ibañez, Santiago, Chile

    Jhosmary Cuadros

  7. Grupo de Bioingeniería, Decanato de Investigación, Universidad Nacional Experimental del Táchira, San Cristóbal 5001, Venezuela

    Jhosmary Cuadros

  8. Department of Electronic Engineering, Universidad Técnica Federico Santa María, Valparaíso, Chile

    Alejandro Weinstein & Matías Zañartu

  9. Department of Sound, Universidad de Chile, Santiago, Chile

    Víctor M. Espinoza

  10. Escuela de Fonoaudiología, Facultad de Ciencias de la Rehabilitación y Calidad de Vida, Universidad San Sebastián, Santiago, Chile

    Pavel Prado

Authors
  1. Lucía Z-Rivera
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  2. Christian Castro
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  3. Jhosmary Cuadros
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  4. Juan P. Cortés
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  5. Alejandro Weinstein
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  6. Víctor M. Espinoza
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  7. Pavel Prado
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  8. Matías Zañartu
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Corresponding authors

Correspondence to Lucía Z-Rivera or Matías Zañartu.

Ethics declarations

Competing Interests

A.W. and M.Z. hold a financial interest in Lanek SPA, a company engaged in the development and commercialization of biomedical devices and technologies. These interests have been reviewed and are managed by Universidad Técnica Federico Santa María in accordance with its conflict-of-interest policies. All other authors declare no competing interests.

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Cite this article

Z-Rivera, L., Castro, C., Cuadros, J. et al. Neural dynamics and acoustic adaptations during the Lombard effect: evidence from EEG and dynamic causal modeling. Sci Rep (2026). https://doi.org/10.1038/s41598-026-49995-x

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  • Received: 31 October 2025

  • Accepted: 17 April 2026

  • Published: 24 April 2026

  • DOI: https://doi.org/10.1038/s41598-026-49995-x

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