Skip to main content

Advertisement

Log in

The acoustic effect of vocal tract adjustments in zebra finches

  • Original Paper
  • Published:
Journal of Comparative Physiology A Aims and scope Submit manuscript

Abstract

Vocal production in songbirds requires the control of the respiratory system, the syrinx as sound source and the vocal tract as acoustic filter. Vocal tract movements consist of beak, tongue and hyoid movements, which change the volume of the oropharyngeal–esophageal cavity (OEC), glottal movements and tracheal length changes. The respective contributions of each movement to filter properties are not completely understood, but the effects of this filtering are thought to be very important for acoustic communication in birds. One of the most striking movements of the upper vocal tract during vocal behavior in songbirds involves the OEC. This study measured the acoustic effect of OEC adjustments in zebra finches by comparing resonance acoustics between an utterance with OEC expansion (calls) and a similar utterance without OEC expansion (respiratory sounds induced by a bilateral syringeal denervation). X-ray cineradiography confirmed the presence of an OEC motor pattern during song and call production, and a custom-built Hall-effect collar system confirmed that OEC expansion movements were not present during respiratory sounds. The spectral emphasis during zebra finch call production ranging between 2.5 and 5 kHz was not present during respiratory sounds, indicating strongly that it can be attributed to the OEC expansion.

This is a preview of subscription content, log in via an institution to check access.

Access this article

Price excludes VAT (USA)
Tax calculation will be finalised during checkout.

Instant access to the full article PDF.

Institutional subscriptions

Fig. 1
Fig. 2
Fig. 3
Fig. 4
Fig. 5
Fig. 6
Fig. 7
Fig. 8
Fig. 9
Fig. 10
Fig. 11

Similar content being viewed by others

References

  • Arneodo EM, Perl YS, Mindlin GB (2011) Acoustic signatures of sound source-tract coupling Phys Rev E-83: art. no. 041920

  • Dooling RJ (1992) Perception of speech sounds by birds. Adv Biosci 83:407–413

    Google Scholar 

  • Dubbeldam JL, den Boer-Visser AM, Bout RG (1997) Organization and efferent connections of the archistriatum of the mallard, Anas platyrhynchos L.: an anterograde and retrograde tracing study. J Comp Neurol 388:632–657

    Article  PubMed  CAS  Google Scholar 

  • Elemans C, Laje R, Mindlin G, Goller F (2010) Smooth operator: avoidance of subharmonic bifurcations through mechanical mechanisms simplifies song motor control in adult zebra finches. J Neurosci 30:13246–13253

    Article  PubMed  CAS  Google Scholar 

  • Fee MS (2002) Measurement of the linear and nonlinear mechanical properties of the oscine syrinx: implications for function. J Comp Physiol A 188:829–839

    Google Scholar 

  • Fletcher N, Riede T, Suthers RA (2006) Model for vocalization by a bird with distensible vocal cavity and open beak. J Acoust Soc Am 119:1005–1011

    Article  PubMed  Google Scholar 

  • Goller F, Larsen ON (1997) A new mechanism of sound generation in songbirds. Proc Natl Acad Sci USA 94:14787–14791

    Article  PubMed  CAS  Google Scholar 

  • Goller F, Mallinckrodt MJ, Torti SD (2004) Beak gape dynamics during song in the zebra finch. J Neurobiol 59:289–303

    Article  PubMed  Google Scholar 

  • Heinz RD, Sachs MB, Sinnott JM (1981) Discrimination of steady-state vowels by blackbirds and pigeons. J Acoust Soc Am 70:699–706

    Article  Google Scholar 

  • Hoese WJ, Podos J, Boetticher NC, Nowicki S (2000) Vocal tract function in birdsong production: experimental manipulation of beak movements. J Exp Biol 203:1845–1855

    PubMed  CAS  Google Scholar 

  • Homberger DG, Meyers RA (1989) Morphology of the lingual apparatus of the domestic chicken, Gallus gallus, with special attention to the structure of the fasciae. Am J Anat 186:217–257

    Article  PubMed  CAS  Google Scholar 

  • Larsen ON, Goller F (2002) Direct observation of syringeal muscle function in songbirds and a parrot. J Exp Biol 205:25–35

    PubMed  Google Scholar 

  • Nowicki S (1987) Vocal tract resonances in oscine bird sound production: evidence from birdsongs in a helium atmosphere. Nature 325:53–55

    Article  PubMed  CAS  Google Scholar 

  • Ohms V, Snelderwaard PC, ten Cate C, Beckers GJL (2010) Vocal tract articulation in zebra finches. PLoS ONE 5:e11923

    Article  PubMed  Google Scholar 

  • Perl YS, Arneodo EM, Amador A, Goller F, Mindlin GB (2011) Reconstruction of physiological instructions from zebra finch song. Phys Rev E 84:051909

    Google Scholar 

  • Podos J, Sherer JK, Peters S, Nowicki S (1995) Ontogeny of vocal-tract movements during song production in song sparrows. Anim Behav 50:1287–1296

    Article  Google Scholar 

  • Prince B, Riede T, Goller F (2011) Sexual dimorphism and bilateral asymmetry of syrinx and vocal tract in the European Starling (Sturnus vulgaris). J Morph 272:1527–1536

    Article  PubMed  Google Scholar 

  • Riede T, Goller F (2010a) Peripheral mechanisms for vocal production in birds—differences and similarities to human speech and singing. Brain Lang 115:69–80

    Article  PubMed  Google Scholar 

  • Riede T, Goller F (2010b) Functional morphology of the sound generating labia in the syrinx of two songbird species. J Anat 216:23–36

    Article  PubMed  Google Scholar 

  • Riede T, Suthers RA (2009) Vocal tract motor patterns and resonance during constant frequency song: the white-throated sparrow. J Comp Physiol A 195:183–192

    Article  Google Scholar 

  • Riede T, Suthers RA, Fletcher N, Blevins W (2006) Songbirds tune their vocal tract to the fundamental frequency of their song. Proc Nat Acad Sci 103:5543–5548

    Article  PubMed  CAS  Google Scholar 

  • Riede T, Fisher JH, Goller F (2010) Sexual dimorphism of the sound generating labia and the cartilaginous framework in the syrinx of zebra finches. PLoS ONE 5:e11368

    Article  PubMed  Google Scholar 

  • Sitt JD, Arneodo EM, Goller F, Mindlin GB (2010) Physiologically driven avian vocal synthesizer. Phys Rev E 81 (3), art. no. 031927

    Google Scholar 

  • Titze IR (1989) On the relation between subglottal pressure and fundamental frequency in phonation. J Acoust Soc Am 85:901–906

    Article  PubMed  CAS  Google Scholar 

  • Westneat MW, Long J, John H, Hoese W, Nowicki S (1993) Kinematics of birdsong: functional correlation of cranial movements and acoustic features in sparrows. J Exp Biol 182:147–171

    PubMed  CAS  Google Scholar 

  • Wild JM, Farabaugh SM (1996) Organization of afferent and efferent projections of the nucleus basalis prosencephali in a passerine, Taeniopygia guttata. J Comp Neurol 365:306–328

    Article  PubMed  CAS  Google Scholar 

  • Wild JM, Krützfeldt NEO (2012) Trigeminal and telencephalic projections to jaw and other upper vocal tract premotor neurons in songbirds: sensorimotor circuitry for beak movements during singing. J Comp Neurol 520:590–605. doi 10.1002/cne.22752

    Google Scholar 

  • Williams H (2001) Choreography of song, dance and beak movements in the zebra finch (Taeniopygia guttata). J Exp Biol 204:3497–3506

    PubMed  CAS  Google Scholar 

  • Williams H, Cynx J, Nottebohm F (1990) Timbre control in zebra finch (Taeniopygia guttata) song syllables. J Comp Psychol 103:366–380

    Article  Google Scholar 

  • Zann RA (1996) Zebra finch: A synthesis of field and laboratory studies. (Illustrated by Michael Bamford). Oxford University Press

  • Zollinger SA, Riede T, Suthers RA (2008) Two-voice complexity from a single side of the syrinx in northern mockingbird Mimus polyglottos vocalizations. J Exp Biol 211:1978–1991

    Article  PubMed  Google Scholar 

  • Zollinger SA, Goller F, Brumm H (2011) Metabolic and respiratory costs of increasing song amplitude in zebra finches. PLoS One 6(9):e23198

    Article  PubMed  CAS  Google Scholar 

Download references

Acknowledgments

This study was funded by National Institutes of Health Grants DC04390 and DC06876. For their help with the X-ray recordings, we thank R. Petersohn and R. Salzer. Joe Leaman helped with the image analysis. Thanks to Neville Fletcher for his permission to use the model. Experiments were approved and conducted in accordance with the Animal Welfare Regulations of the state of Thuringa, Germany (Reg. No. 02-021/07) and the IACUC of the University of Utah.

Author information

Authors and Affiliations

Authors

Corresponding author

Correspondence to Tobias Riede.

Rights and permissions

Reprints and permissions

About this article

Cite this article

Riede, T., Schilling, N. & Goller, F. The acoustic effect of vocal tract adjustments in zebra finches. J Comp Physiol A 199, 57–69 (2013). https://doi.org/10.1007/s00359-012-0768-4

Download citation

  • Received:

  • Revised:

  • Accepted:

  • Published:

  • Issue Date:

  • DOI: https://doi.org/10.1007/s00359-012-0768-4

Keywords

Navigation