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  • 1
    Electronic Resource
    Electronic Resource
    Springer
    Naturwissenschaften 58 (1971), S. 627-627 
    ISSN: 1432-1904
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology , Chemistry and Pharmacology , Natural Sciences in General
    Type of Medium: Electronic Resource
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  • 2
    Electronic Resource
    Electronic Resource
    Springer
    Journal of comparative physiology 186 (2000), S. 413-423 
    ISSN: 1432-1351
    Keywords: Key words Medial superior olive ; Interaural time ; difference ; Receptive field ; Precedence effect ; Temporal processing
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology , Medicine
    Notes: Abstract Traditionally, the medial superior olive, a mammalian auditory brainstem structure, is considered to encode interaural time differences, the main cue for localizing low-frequency sounds. Detection of binaural excitatory and inhibitory inputs are considered as an underlying mechanism. Most small mammals, however, hear high frequencies well beyond 50 kHz and have small interaural distances. Therefore, they can not use interaural time differences for sound localization and yet possess a medial superior olive. Physiological studies in bats revealed that medial superior olive cells show similar interaural time difference coding as in larger mammals tuned to low-frequency hearing. Their interaural time difference sensitivity, however, is far too coarse to serve in sound localization. Thus, interaural time difference sensitivity in medial superior olive of small mammals is an epiphenomenon. We propose that the original function of the medial superior olive is a binaural cooperation causing facilitation due to binaural excitation. Lagging inhibitory inputs, however, suppress reverberations and echoes from the acoustic background. Thereby, generation of antagonistically organized temporal fields is the basic and original function of the mammalian medial superior olive. Only later in evolution with the advent of larger mammals did interaural distances, and hence interaural time differences, became large enough to be used as cues for sound localization of low-frequency stimuli.
    Type of Medium: Electronic Resource
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  • 3
    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).
    Type of Medium: Electronic Resource
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  • 4
    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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  • 5
    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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  • 6
    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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  • 7
    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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  • 8
    Electronic Resource
    Electronic Resource
    Springer
    Journal of comparative physiology 152 (1983), S. 421-432 
    ISSN: 1432-1351
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology , Medicine
    Notes: Summary 1. When catching flying prey under laboratory conditionsRhinolophus ferrumequinum typically emit FM-CF-FM signals (Fig. 2). Except for the last two sounds during approach and final buzz the FM-parts are fainter than the CF-component by a factor of 0.76+-14 (Fig. 1). The final FM-part was undetectable in some signals emitted during approach (Fig. 3). 2. In obstacle avoidance flights both, preceding and final FM-parts are prominent and louder than the CF-part by a factor of 1.14 to 1.63 (Fig. 1 and 3). Bandwidths of the FM-components increased from ca. 3.5 to 12 kHz for the starting and from 12 to 20 kHz on the average for the final FM-sweep (Table 1). 3. In the open field during cruising flightsNyctalus noctula emits pure tones of 22.5 to 25.0 kHz without any frequency modulated components and a duration of 10 to 50 ms (Fig. 4). Brief frequency modulated signals sweeping from ca. 50 to 20 kHz in about 1–2 ms are emitted during pursuit of prey (Fig. 4). 4. Under laboratory conditionsNyctalus noctula does not emit pure tones and is not able to catch flying prey in a flight chamber 10.5×3.5×2.15 m in size. During flights towards a landing platformNyctalus noctula invariably emits brief frequency modulated pulses. During an individual flight the structure is not changed (Fig. 5). 5. InNyctalus noctula specific features of the echolocation pulses, e.g. frequency range swept through, presence of harmonics and double pulses (Fig. 6) are maintained during an individual flight. These specific characteristics of the signal may be used to identify echoes belonging to its own emitted echolocation pulse.
    Type of Medium: Electronic Resource
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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 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.
    Type of Medium: Electronic Resource
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