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  • 1
    Electronic Resource
    Electronic Resource
    Springer
    Journal of comparative physiology 125 (1978), S. 217-225 
    ISSN: 1432-1351
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology , Medicine
    Notes: Summary The responses of 230 single neurons in the inferior colliculus of the horseshoebat to single tones have been studied, emphasizing systematic analysis of the effective frequency bands, dynamic properties and the time course of responses. Distribution of the units' best excitatory frequencies (BEF) is: low frequency neurons 23% (BEF 3–65 kHz); FM-frequency neurons 25% (BEF 65–81 kHz, i.e., frequencies occurring in the FM-part of the bat's echo signal); filter neurons 45% (BEF 81–88 kHz, i.e., frequencies occurring in the stabilized CF-part of the bat's echo=reference frequency (RF)); high frequency neurons about 7% (BEF 〉 88 kHz). Tuning curves show conventional shapes (Fig. 1), apart from those of filter neurons, which are extremely narrow. Accordingly, Q10dB-values (BEF divided by the bandwidth of the tuning curve at 10 dB above threshold) are 80–450 in filter neurons (Fig. 2). Response patterns (Fig. 3) are similar to those of Nucleus cochlearis units (transient, sustained, negative and complex responders) with an increased percentage of complex responders up to 38% and a decreased number of transient responders. All types of spike-count functions are found (Fig. 4); nonmonotonic ones dominating. Maximal spike counts are not at the BEF but a few kHz below. Distinct upper thresholds, especially at the BEF of filter neurons (Fig. 5) lead to abrupt changes in activity by slightly shifting stimulus frequency or intensity. The hallmark of inferior colliculus neurons is inhibition, disclosed by distinct inhibitory areas enfolding and overlapping excitatory ones (Figs. 3 and 5). Duration of inhibition varies with stimulus frequency, but is largely independent of stimulus duration (Fig. 6), whereas rebound of inhibition depends on stimulus duration building up periodic rebound activities, if stimulus duration is lengthened. In addition, there are neurons responding only periodically, regardless of stimulus frequency and intensity (Fig. 7). Inhibition is discussed in terms of improving the neuronal signal/spontaneous noise ratio and altering responsiveness of neurons after stimulation, so that these neurons may be suited to time processing in the acoustic pathway.
    Type of Medium: Electronic Resource
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  • 2
    Electronic Resource
    Electronic Resource
    Springer
    Journal of comparative physiology 154 (1984), S. 133-142 
    ISSN: 1432-1351
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology , Medicine
    Notes: Summary 1. Audiograms are recorded from one non-echolocating and nine echolocating sympatrically living bat species of South India. These species areCynopterus sphinx (non-echolocating),Tadarida aegyptiaca, Taphozous melanopogon, T. kachhensis, Rhinopoma hardwickei, Pipistrellus dormeri, P. mimus, Hipposideros speoris, H. bicolor andMegaderma lyra. 2. InRhinopoma hardwickei a highly sensitive frequency range was found which is narrowly tuned to the frequency band of the bat's CF-echolocation call (32–35 kHz, Fig. 3). In hipposiderids a ‘filter’ narrowly tuned to the frequency of the CF-part of the CF-FM echolocation sounds (137.5 kHz inH. speoris and 151.5 kHz inH. bicolor, Fig. 5) could be recorded from deeper parts of IC. 3. In the echolocating species the best frequency of the audiograms closely matched with that frequency range in the echolocation calls containing most energy. 4. In bat species foraging flying prey best frequencies of audiograms and height of preferred foraging areas are inversely related, i.e. bat species hunting high above canopy have lower best frequencies than those foraging close to or within canopy (Fig. 6). 5. A hypothesis is forwarded explaining how fluttering target detection by constant frequency echolocation might have evolved from long distance echolocation by pure tone signals.
    Type of Medium: Electronic Resource
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  • 3
    Electronic Resource
    Electronic Resource
    Springer
    Journal of comparative physiology 160 (1987), S. 1-1 
    ISSN: 1432-1351
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology , Medicine
    Type of Medium: Electronic Resource
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  • 4
    Electronic Resource
    Electronic Resource
    Springer
    Journal of comparative physiology 168 (1991), S. 45-51 
    ISSN: 1432-1351
    Keywords: Hearing ; Chiroptera ; Desmodus Inferior colliculus ; Tonotopy
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology , Medicine
    Notes: Summary 1. Within the tonotopic organization of the inferior colliculus two frequency ranges are well represented: a frequency range within that of the echolocation signals from 50 to 100 kHz, and a frequency band below that of the echolocation sounds, from 10 to 35 kHz. The frequency range between these two bands, from about 40 to 50 kHz is distinctly underrepresented (Fig. 3B). 2. Units with BFs in the lower frequency range (10–25 kHz) were most sensitive with thresholds of -5 to -11 dB SPL, and units with BFs within the frequency range of the echolocation signals had minimal thresholds around 0 dB SPL (Fig. 1). 3. In the medial part of the rostral inferior colliculus units were encountered which preferentially or exclusively responded to noise stimuli. — Seven neurons were found which were only excited by human breathing noises and not by pure tones, frequency modulated signals or various noise bands. These neurons were considered as a subspeciality of the larger sample of noise-sensitive neurons. — The maximal auditory sensitivity in the frequency range below that of echolocation, and the conspicuous existence of noise and breathing-noise sensitive units in the inferior colliculus are discussed in context with the foraging behavior of vampire bats.
    Type of Medium: Electronic Resource
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  • 5
    Electronic Resource
    Electronic Resource
    Springer
    Journal of comparative physiology 115 (1977), S. 119-133 
    ISSN: 1432-1351
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology , Medicine
    Notes: Summary 1. In horseshoe bats temporal response patterns to pure tone stimuli (10–100 kHz, 20 ms duration, 0.5 ms rise/fall-time) of 149 cochlear nucleus units (DCN and PVCN) have been recorded. 2. Distribution of the units' Best Frequencies (BF): low frequency neurons 26% (BF 10–65 kHz); FM-frequency neurons 20% (BF 65–81 kHz, i.e. frequencies occurring in the FM-part of the bat's echo signal); filter frequency neurons 52% (BF 81–88 kHz, i.e. frequencies occurring in the CF-part of the bat's echo signal); high frequency neurons 2% (BF 〉 88 kHz) (Table 1). 3. According to PST-histograms the neurons were classified as: sustained responders (28%, Fig. 1D, E); transient responders (51%, Fig. 1A–C); negative responders (4%, Fig. 1F) and complex responders (17%, Fig. 2–4). In the latter class response patterns drastically change with stimulus frequency and intensity. These units have suppressory sidebands on one or both sides of the excitatory field, sometimes overlapping and enclosing the excitatory area (Fig. 2 and 4). Frequently excitatory response patterns display simultaneous inhibitory processes the latency and duration of which depend on stimulus parameters. 4. In a few complex responders two or more excitatory areas exist, the BF of which may be harmonically related (Fig. 3 and 4). 5. Tuning curves of four auditory nerve fibers are reported showing two separate excitatory areas: a broad less sensitive one from 37 to 79 kHz (low frequency tail) and a narrow, more sensitive one from 82 to 90 kHz (Fig. 5).
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  • 6
    Electronic Resource
    Electronic Resource
    Springer
    Journal of comparative physiology 163 (1988), S. 271-285 
    ISSN: 1432-1351
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology , Medicine
    Notes: Summary The tonotopic organization of the inferior colliculus (IC) in two echolocating bats,Hipposideros speoris andMegaderma lyra, was studied by multiunit recordings. InHipposideros speoris frequencies below the range of the echolocation signals (i.e. below 120 kHz) are compressed into a dorsolateral cap about 400–600 Μm thick. Within this region, neuronal sheets of about 4–5 Μm thickness represent a 1 kHz-band. In contrast, the frequencies of the echolocation signals (120–140 kHz) are overrepresented and occupy the central and ventral parts of the IC (Fig. 3). In this region, neuronal sheets of about 80 Μm thickness represent a 1 kHz-band. The largest 1 kHz-slabs (400–600 Μm) represent frequencies of the pure tone components of the echolocation signals (130–140 kHz). The frequency of the pure tone echolocation component is specific for any given individual and always part of the overrepresented frequency range but did not necessarily coincide with the BF of the thickest isofrequency slab. Thus hipposiderid bats have an auditory fovea (Fig. 10). In the IC ofMegaderma lyra the complete range of audible frequencies, from a few kHz to 110 kHz, is represented in fairly equal proportions (Fig. 7). On the average, a neuronal sheet of 30 Μm thickness is dedicated to a 1 kHz-band, however, frequencies below 20 kHz, i.e. below the range of the echolocation signals, are overrepresented. Audiograms based on thresholds determined from multiunit recordings demonstrate the specific sensitivities of the two bat species. InHipposideros speoris the audiogram shows two sensitivity peaks, one in the nonecholocating frequency range (10–60 kHz) and one within the auditory fovea for echolocation (130–140 kHz).Megaderma lyra has extreme sensitivity between 15–20 kHz, with thresholds as low as −24 dB SPL, and a second sensitivity peak at 50 kHz (Fig. 8). InMegaderma lyra, as in common laboratory mammals, Q10dB-values of single units do not exceed 30, whereas inHipposideros speoris units with BFs within the auditory fovea reach Q10dB-values of up to 130. InMegaderma lyra, many single units and multiunit clusters with BFs below 30 kHz show upper thresholds of 40–50 dB SPL and respond most vigorously to sound intensities below 30 dB SPL (Fig. 9). Many of these units respond preferentially or exclusively to noise. These features are interpreted as adaptations to detection of prey-generated noises. The two different tonotopic arrangements (compare Figs. 3 and 7) in the ICs of the two species are correlated with their different foraging behaviours. It is suggested that pure tone echolocation and auditory foveae are primarily adaptations to echo clutter rejection for species foraging on the wing close to vegetation.
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  • 7
    ISSN: 1432-1351
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology , Medicine
    Notes: Summary 1. Two hipposiderid bats,H. bicolor andH. speoris, were observed in their natural foraging areas in Madurai (South India). Both species hunt close together near the foliage of trees and bushes but they differ in fine structure of preferred hunting space:H. bicolor hunts within the foliage, especially whenH. speoris is active at the same time, whereasH. speoris never flies in dense vegetation but rather in the more open area (Fig. 1, Table 1). 2. Both species emit CF/FM-sounds containing only one harmonic component in almost all echolocation situations. The CF-parts of CF/FM-sounds are species specific within a band of 127–138 kHz forH. speoris and 147–159 kHz forH. bicolor (Tables 2 and 3). 3. H. speoris additionally uses a complex harmonic sound during obstacle avoidance and during laboratory tests for Doppler shift compensation.H. bicolor consistently emits CF/FM-sounds in these same situations (Fig. 2). 4. Both hipposiderid bats respond to Doppler shifts in the returning echoes by lowering the frequency of the emitted sounds (Fig. 3). However, Doppler compensations are incomplete as the emitted frequencies are decreased by only 55% and 56% (mean values) of the full frequency shifts byH. speoris andH, bicolor, respectively. 5. The differences in Doppler shift compensation, echolocating and hunting behavior suggest thatH. speoris is less specialized on echolocation with CF/FM-sounds thanH. bicolor.
    Type of Medium: Electronic Resource
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  • 8
    Electronic Resource
    Electronic Resource
    Springer
    Journal of comparative physiology 159 (1986), S. 403-413 
    ISSN: 1432-1351
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology , Medicine
    Notes: Summary 1. The echolocating ‘long CF/FM-bat’Rhinolophus rouxi and the ‘short CF/FM-bats’Hipposideros bicolor andHipposideros speoris were tested for catching responses to moving and non-moving targets. 2. Under our experimental conditions (freshly caught caged bats in a natural environment)Rhinolophus rouxi andHipposideros speoris only responded to insects of any sort that were beating their wings. The bats showed no reactions whatsoever to nonmoving insects or those walking on the floor or the sides of the cage. 3. Hipposideros bicolor responded in the same way as the above species to wingbeating insects but in addition also attacked walking insects. In 27 presentations 15 walking insects were caught (Fig. 2). 4. Rhinolophus rouxi, Hipposideros speoris andHipposideros bicolor also detected, approached and seized tethered cockroaches hanging from the ceiling when these were vibrating up and down (Fig. 3). This indicates that any oscillating movement and not specific aspects of wing beating were the key releasers for catching behaviour in all three species. However, a wing beating insect is strongly preferred over a vibrating one in all three species (Fig. 4). 5. Rhinolophus rouxi, Hipposideros speoris andHipposideros bicolor attacked and seized a dead bait when it was associated with a wing beating device (Fig. 1). All three species responded effectively to beat frequencies as low as 10 beats/s (peak-to-peak amplitude of the wing excursion 20 mm). For lower frequencies the response rates rapidly deteriorated (Fig. 5). 6. Horseshoe bats no longer responded to wing beats of 5 beats/s when the wing beat amplitude was 2 to 1 mm or to wing beats of 2 to 1 beats/s when the amplitude was 3 mm or lower (Fig. 6). This suggests that the speed of the wing is a critical parameter. From these data we infer that the threshold for the catching responses is at a wing speed of about 2 to 1 cm/s. 7. In horseshoe bats (experimental tests) and the two hipposiderid species (behavioural observations) one single wing beat was enough to elicit a catching response (Fig. 8). 8. It is concluded that ‘long’ and ‘short’ CF/ FM-bats feature a similar responsiveness to fluttering targets. The sensitivity to oscillating movements is considered as an effective detection mechanism for any sort of potential prey.
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  • 9
    Electronic Resource
    Electronic Resource
    Springer
    Journal of comparative physiology 165 (1989), S. 755-769 
    ISSN: 1432-1351
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology , Medicine
    Notes: Summary The postnatal development of midbrain tonotopy was investigated in the inferior colliculus (IC) of the south Indian CF-FM batHipposideros speoris. The developmental progress of the three-dimensional frequency representation was determined by systematic stereotaxic recordings of multiunit clusters from the 1st up to the 7th postnatal week. Additional developmental measures included the tuning characteristics of single units (Figs. 3f; 4f; 5f), the analysis of the vocalised pulse repertoire (Figs. 3e, 4e, 5e), and morphometric reconstructions of the brains of all experimental animals (Fig. 1). The maturation of auditory processing could be divided into two distinct, possibly overlapping developmental periods: First, up to the 5th week, the orderly tonotopy in the IC developed, beginning with the low frequency representation and progressively adding the high frequency representation. With regard to the topology of isofrequency sheets within the IC, maturation progresses from dorsolateral to ventromedial (Figs. 3c, 4c). At the end of this phase the entire IC becomes specialised for narrowly tuned and sensitive frequency processing. This includes the establishment of the ‘auditory fovea’, i.e. the extensive spatial representation of a narrow band of behaviorally relevant frequencies in the ventromedial part of the IC. In the 5th postnatal week the auditory fovea is concerned with frequencies from 100–118 kHz (Fig. 4c, d). During subsequent development, the frequency tuning of the auditory fovea increases by 20–25 kHz and finally attains the adult range of ca. 125–140 kHz. During this process, neither the bandwidth of the auditory fovea (15–20 kHz) nor the absolute sensitivity of its units (ca. 50 dB SPL) were changed. Further maturation occurred at the single unit level : the sharpness of frequency tuning increased from the 5th to the 7th postnatal weeks (Q-10-dB-values up to 30–60), and upper thresholds emerged (Figs. 4f, 5f). Although in the adult the frequency of the auditory fovea matches that of the vocalised pulses, none of the juvenile bats tested from the 5th to the 7th weeks showed such a frequency match between vocalisation and audition (Figs. 4e, 5e). The results show that postnatal maturation of audition in hipposiderid bats cannot be described by a model based on a single developmental parameter.
    Type of Medium: Electronic Resource
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  • 10
    Electronic Resource
    Electronic Resource
    Springer
    Journal of comparative physiology 74 (1971), S. 153-155 
    ISSN: 1432-1351
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology , Medicine
    Notes: Summary Collicular evoked potentials in Rhinolophus ferrum equinum show very prominent responses to the final frequency modulated part of a acoustic stimulus, simulating the natural echolocation sound.
    Type of Medium: Electronic Resource
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