Literature DB >> 3430416

Ontogenesis of the echolocation system in the rufous horseshoe bat, Rhinolophus rouxi (audition and vocalization in early postnatal development).

R Rübsamen1.   

Abstract

1. The development of vocalization and hearing was studied in Sri Lankan horseshoe bats (Rhinolophus rouxi) during the first postnatal month. The young bats were caught in a nursing colony of rhinolophids in which birth took place within a two week period. 2. The new-born bats emitted isolation calls through the mouth. At the beginning these calls consisted of pure tones with frequencies below 10 kHz (Fig. 1). During the first postnatal week the call frequency increased to about 15 kHz, and the fundamental was augmented by two to four harmonics. No evoked potentials to pure tone stimuli could be elicited in the inferior colliculus of this age group, i.e., auditory processing at the midbrain level was not demonstrable. 3. Evoked potentials were first recorded in the second week, broadly tuned to 15-45 kHz, with a maximum sensitivity between 15-25 kHz. In the course of the second week, however, higher frequencies up to 60 kHz became progressively incorporated into the audiogram (Fig. 3). The fundamental frequency of the multiharmonic isolation calls, emitted strictly through the mouth, increased to about 20 kHz. 4. In the bats' third postnatal week an increased hearing sensitivity (auditory filter) emerged, sharply tuned at frequencies between 57 and 60 kHz (Fig. 4e). The same individuals were also the first to emit long constant frequency echolocation calls through the nostrils (Fig. 4c). The energy of the calls was arranged in harmonic frequency bands with the second harmonic exactly tuned to the auditory filter. These young bats continued to emit isolation calls through the mouth, which were, however, not harmonically related to the echolocation calls (Fig. 4b, d). 5. During the fourth week, both the auditory filter and the matched echolocation pulses (the second harmonic) shifted towards higher frequencies (Fig. 5). During the fifth week the fundamental frequency of the calls was progressively attenuated, and both the second harmonic of the pulses and the auditory filter reached the frequency range typical for adult bats of 73-78 kHz (Fig. 6). 6. The development of audition and vocalization is discussed with regard to possible interactions of both subsystems, and their incorporation into the active orientation system of echolocation.

Mesh:

Year:  1987        PMID: 3430416     DOI: 10.1007/BF00610231

Source DB:  PubMed          Journal:  J Comp Physiol A            Impact factor:   1.836


  15 in total

1.  Inferior colliculus. II. Development of tuning characteristics and tonotopic organization in central nucleus of the neonatal cat.

Authors:  L M Aitkin; D R Moore
Journal:  J Neurophysiol       Date:  1975-09       Impact factor: 2.714

2.  SINGLE-CELL RESPONSES IN STRIATE CORTEX OF KITTENS DEPRIVED OF VISION IN ONE EYE.

Authors:  T N WIESEL; D H HUBEL
Journal:  J Neurophysiol       Date:  1963-11       Impact factor: 2.714

3.  Neonatal vocalizations in bats of eight genera.

Authors:  E Gould
Journal:  J Mammal       Date:  1975-02       Impact factor: 2.416

4.  Behavior programs and evolutionary strategies.

Authors:  E Mayr
Journal:  Am Sci       Date:  1974 Nov-Dec       Impact factor: 0.548

5.  Ultrasonic communication in rodents.

Authors:  G D Sewell
Journal:  Nature       Date:  1970-07-25       Impact factor: 49.962

6.  Ontogenetic changes in frequency mapping of a mammalian ear.

Authors:  D M Harris; P Dallos
Journal:  Science       Date:  1984-08-17       Impact factor: 47.728

7.  An HRP-study of the frequency-place map of the horseshoe bat cochlea: morphological correlates of the sharp tuning to a narrow frequency band.

Authors:  M Vater; A S Feng; M Betz
Journal:  J Comp Physiol A       Date:  1985-11       Impact factor: 1.836

8.  Silver staining of myelin by means of physical development.

Authors:  F Gallyas
Journal:  Neurol Res       Date:  1979       Impact factor: 2.448

9.  Development of inferior colliculus response properties in C57BL/6J mouse pups.

Authors:  A Shnerson; J F Willott
Journal:  Exp Brain Res       Date:  1979-10       Impact factor: 1.972

10.  Morphological changes in the cochlea of the mouse after the onset of hearing.

Authors:  H J Kraus; K Aulbach-Kraus
Journal:  Hear Res       Date:  1981-03       Impact factor: 3.208

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  15 in total

1.  Audiovocal interactions during development? Vocalisation in deafened young horseshoe bats vs. audition in vocalisation-impaired bats.

Authors:  R Rübsamen; M Schäfer
Journal:  J Comp Physiol A       Date:  1990-12       Impact factor: 1.836

2.  Ontogenesis of auditory fovea representation in the inferior colliculus of the Sri Lankan rufous horseshoe bat, Rhinolophus rouxi.

Authors:  R Rübsamen; M Schäfer
Journal:  J Comp Physiol A       Date:  1990-12       Impact factor: 1.836

3.  Ontogenesis of tonotopy in inferior colliculus of a hipposiderid bat reveals postnatal shift in frequency-place code.

Authors:  R Rübsamen; G Neuweiler; G Marimuthu
Journal:  J Comp Physiol A       Date:  1989-10       Impact factor: 1.836

Review 4.  Postnatal development of central auditory frequency maps.

Authors:  R Rübsamen
Journal:  J Comp Physiol A       Date:  1992-02       Impact factor: 1.836

5.  Behavioral auditory thresholds in neonate lesser spear-nosed bats, Phyllostomus discolor.

Authors:  K H Esser; U Schmidt
Journal:  Naturwissenschaften       Date:  1990-06

6.  Development of echolocation calls and neural selectivity for echolocation calls in the pallid bat.

Authors:  Khaleel A Razak; Zoltan M Fuzessery
Journal:  Dev Neurobiol       Date:  2014-08-28       Impact factor: 3.964

7.  Testing the role of preBötzinger Complex somatostatin neurons in respiratory and vocal behaviors.

Authors:  Srinivasan Tupal; Michael A Rieger; Guang-Yi Ling; Thomas J Park; Joseph D Dougherty; Ann K Goodchild; Paul A Gray
Journal:  Eur J Neurosci       Date:  2014-07-21       Impact factor: 3.386

8.  Development of echolocation and communication vocalizations in the big brown bat, Eptesicus fuscus.

Authors:  Jenna A Monroy; Matthew E Carter; Kimberly E Miller; Ellen Covey
Journal:  J Comp Physiol A Neuroethol Sens Neural Behav Physiol       Date:  2011-02-15       Impact factor: 1.836

9.  Distress call-induced gene expression in the brain of the Indian short-nosed fruit bat, Cynopterus sphinx.

Authors:  Ambigapathy Ganesh; Hanumanthan Raghuram; Parthasarathy T Nathan; Ganapathy Marimuthu; Koilmani Emmanuvel Rajan
Journal:  J Comp Physiol A Neuroethol Sens Neural Behav Physiol       Date:  2010-02       Impact factor: 1.836

10.  Development of hearing in the big brown bat.

Authors:  Doreen Möckel; Thomas Groulx; Paul A Faure
Journal:  J Comp Physiol A Neuroethol Sens Neural Behav Physiol       Date:  2020-11-16       Impact factor: 1.836

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