Constant Frequency Component Research Articles

Distribution of combination-sensitive neurons in the ventral fringe area of the auditory cortex of the mustached bat

1. The orientation sound (pulse) of the mustached bat, Pteronotus parnellii parnellii, consists of long constant-frequency components (CF1-4) and short frequency-modulated components (FM1-4). The auditory cortex of this bat contains several combination-sensitive areas: FM-FM, DF, VA, VF, and CF/CF. The FM-FM area consists of neurons tuned to a combination of the pulse FM1 and the echo FMn (n = 2, 3, or 4) and has an echo-delay (target-range) axis. Our preliminary anatomical studies with tritiated amino acids suggest that the FM-FM area projects to the dorsal fringe (DF) area, which in turn projects to the ventral fringe (VF) area. The aim of our study was to characterize the response properties of VF neurons and to explore the functional organization of the VF area. Acoustic stimuli delivered to the bats were CF tones, FM sounds, and their combinations mimicking the pulse emitted by the mustached bat and the echo. 2. Like the FM-FM and DF areas, the VF area is composed of three types of FM-FM combination-sensitive neurons: FM1-FM2, FM1-FM3, and FM1-FM4. These neurons show little or no response to a pulse alone, echo alone, single CF tone or single FM sound. They do, however, show a strong facilitative response to a pulse-echo pair with a particular echo delay. The essential components in the pulse-echo pair for facilitation are the FM1 of the pulse and the FMn of the echo.(ABSTRACT TRUNCATED AT 250 WORDS)

Combination-sensitive neurons in the ventroanterior area of the auditory cortex of the mustached bat.

1. Because the ventroanterior (VA) area is one of the target areas of the FM-FM area in the auditory cortex of the mustached bat, Pteronotus parnellii parnellii, response properties of combination-sensitive neurons in this area were studied with constant-frequency (CF) tones, frequency-modulated (FM) sounds, and sounds similar to the bat's biosonar signal (pulse), which consisted of long CF components (CF1-4) and short FM components (FM1-4). CF1-4 and FM1-4 are the components in the four harmonics (H1-4) of the pulse. 2. Combination-sensitive neurons are clustered in a small area immediately anteroventral to the Doppler-shifted CF processing (DSCF) area and posteroventral to the anterior division of the primary auditory cortex. Because this cluster in the VA area is small, it was difficult to record a sufficient number of combination-sensitive neurons to explore the functional organization of the cluster, but it was found that the response properties of these VA neurons were unique. 3. Combination-sensitive neurons in the VA area are tuned to particular combinations of signal elements similar to the first and second harmonics of the pulse and/or echo. Unlike neurons in the FM-FM, dorsal fringe (DF), and CF/CF areas, no neurons in the VA area are tuned to the signal elements in the first and third or fourth harmonics. 4. The great majority of combination-sensitive neurons in the VA area can not be easily classified into either FM-FM or CF/CF neurons, because they show facilitative responses to combinations of CF1/CF2, FM1-FM2, and FM1-CF2. Therefore, they are called H1-H2 neurons. In the FM-FM and CF/CF areas, all the neurons could be easily classified as FM-FM or CF/CF. This uniqueness of H1-H2 neurons is related to the fact that their best frequencies for facilitation are predominantly between 61.0 and 62.0 kHz, i.e., within the frequency range of stabilized Doppler-shifted echo CF2. 5. In addition to 27 H1-H2 neurons, 7 FM1-FM2 neurons were also recorded in the VA area. The best delays of these H1-H2 and FM1-FM2 neurons measured with FM1-FM2 pairs are between 1 and 10 ms. Unlike neurons in the FM-FM and DF areas, their delay-tuning curves are very broad, even if their best delays are short, and extend beyond zero delay to several millisecond "negative" delays of the FM2 from the FM1, i.e., several millisecond delays of the FM1 from the FM2.(ABSTRACT TRUNCATED AT 400 WORDS)

The acoustic role of tracheal chambers and nasal cavities in the production of sonar pulses by the horseshoe bat, Rhinolophus hildebrandti.

The acoustic role of the enlarged, bony, nasal cavities and rigid tracheal chambers in the horseshoe bat, Rhinolophus hildebrandti (Fig. 2) was investigated by determining the effect of their selective filling on the nasally emitted sonar pulse and on the sound traveling backwards down the trachea. Normal sonar signals of this bat contain a long constant frequency component with most energy in the second harmonic at about 48 kHz. The fundamental is typically suppressed 20 to 30 dB below the level of the second harmonic (Fig. 1). None of the experimental manipulations described affected the frequency of the sonar signal fundamental. Filling the dorsal and both lateral tracheal chambers had little effect on the emitted vocalization, but caused the level of the fundamental component in the trachea to increase 15 to 19 dB in most bats (Table 2). When only the dorsal chamber or only the two lateral chambers were filled, the effect was less striking and more variable (Tables 3 and 4), suggesting that the tracheal fundamental is normally suppressed by acoustic interaction between these three cavities. Filling the enlarged dorsal nasal cavities had no effect on the tracheal sound. The effect of this treatment on the nasally emitted sonar pulse was inconsistent. Sometimes the fundamental increased 10 to 12 dB, other times the intensity of all harmonics decreased; in still other cases the second, third or fourth harmonic increased, but the fundamental remained unchanged (Tables 5, 6, and 7). When bats were forced to vocalize through the mouth, by sealing the nostrils, there was a prominent increase in the level of the emitted fundamental (10 to 21 dB) and in the fourth harmonic (6 to 17 dB). In one instance there was also a significant increase in the level of the third harmonic (Tables 8 and 9). The supraglottal tract thus filters the fundamental from the nasally emitted sonar signal, although the role of the inflated nasal cavities in this process is unclear. We conclude that a high glottal impedance acoustically isolates the subglottal from the supraglottal vocal tract. The tracheal chambers do not affect the emitted sonar signal, but may attenuate the fundamental in the trachea and prevent it from being reflected from the lungs back towards the cochlea. It may be important to prevent the reflected fundamental from stimulating the cochlea, via tissue conduction, along multiple indirect pathways which would temporally smear cochlear stimulation.(ABSTRACT TRUNCATED AT 400 WORDS)

Discrimination of fluttering targets by the FM-batPipistrellus stenopterus?

Five bats of the speciesPipistrellus stenopterus were trained in a two-alternative forced-choice procedure to discriminate between two fluttering targets. The positive target simulated an insect with a 50 Hz wingbeat rate. The negative target was varied between 0 and 48 Hz. The bats were able to discriminate a target with 41 Hz from a target with 50 Hz with 75% correct choices. In the discrimination task, they typically emitted echolocation calls of 2–4 ms duration sweeping from 60 kHz to 30 kHz. The duty cycle (i.e. fraction of time filled with echolocation sounds) increased when the targets fluttered, but was always lower than 3%. The performance ofP. stenopterus in discriminating fluttering targets is comparable to that of bats emitting longer sounds with constant-frequency (CF) components and a higher duty cycle. The FM-sounds ofP. stenopterus are short compared with the period of the fluttering targets, and therefore make it difficult for the animal to measure the time interval between two acoustic glints. Other cues may be prominent, such as the frequency modulation by Doppler shifts from the moving blades.

The personalized auditory cortex of the mustached bat: adaptation for echolocation.

1. In the mustached bat, Pteronotus parnellii, the "resting" frequency of the constant-frequency component of the second harmonic (CF2) of the orientation sound (biosonar signal) is different among individuals within a range from 59.69 to 63.33 kHz. The standard deviation of CF2 resting frequency is 0.091 kHz on the average for individual bats. The male's CF2 resting frequency (61.250 +/- 0.534 kHz, n = 58) is 1.040 kHz lower than the female's (62.290 +/- 0.539 kHz, n = 58) on the average. Females' resting frequencies measured in December are not different from those measured in April when almost all of them are pregnant. Therefore, the orientation sound is sexually dimorphic. 2. In the DSCF (Doppler-shifted CF processing) area of the auditory cortex, tonotopic representation differs among individual bats. The higher the CF2 resting frequency of the bat's own sound, the higher the frequencies represented in the DSCF area of that bat. There is a unique match between the tonotopic representation and the CF2 resting frequency. This match indicates that the auditory cortex is "personalized" for echolocation and that the CF2 resting frequency is like a signature of the orientation sound. 3. If a bat's resting frequency is normalized to 61.00 kHz, the DSCF area overrepresents 60.6-62.3 kHz. The central region of this overrepresented band is 61.1-61.2 kHz. This focal band matches the "reference" frequency to which the CF2 frequency of a Doppler-shifted echo is stabilized by Doppler-shift compensation. 4. Since DSCF neurons are extraordinarily sharply tuned in frequency, the personalization of the auditory cortex or system is not only suited for the detection of wing beats of insects, but also for the reduction of the masking effect on echolocation of consepecific's biosonar signals. 5. Because the orientation sound is sexually dimorphic and the auditory cortex is personalized, the tonotopic representation of the auditory cortex is also sexually dimorphic.

Topographic representation of vocal frequency demonstrated by microstimulation of anterior cingulate cortex in the echolocating bat, Pteronotus parnelli parnelli.

1. A midline region of brain dorsal and anterior to the corpus callosum, presumably anterior cingulate cortex, has been explored for its role in the production of vocalization in the mustached bat, Pteronotus p. parnelli. 2. Vocalizations elicited by microstimulation were virtually indistinguishable from natural biosonar sounds. The spectral content, relative intensity of harmonic components, and durations of emitted pulses are comparable to spontaneous emissions. 3. The frequencies of elicited vocalizations were within the range typically used by the mustached bat during Doppler-shift compensation. The frequency of the second-harmonic constant-frequency component (CF2) covered the range from 57-62 kHz, but was most commonly emitted at frequencies of 59-61 kHz. 4. An increase in the frequency of vocalizations over a number of consecutive pulses towards a steady-state plateau is evident in both spontaneous vocalizations and emissions elicited by microstimulation just above threshold. Increasing the stimulus intensity caused the frequency of emissions to approach the steady state more rapidly. 5. The anterior cingulate cortex appears to be organized topographically for increasing frequency of elicited biosonar sounds along a rostrocaudal axis. The area from which biosonar emissions were elicited was overrepresented for a 2 kHz band of frequencies just below the bats' CF2 resting frequency. Audible vocalizations with a complex spectrum resembling social cries can also be elicited by microstimulation, but only in an area that is adjacent and posterior to the biosonar region. 6. Some examples of both elicited and spontaneous vocalizations contained a relative intensity pattern of the harmonic components which deviated from the typical pattern. This suggests that mustached bats are capable of actively altering the spectrum of their pulses to subserve different tasks in echolocation.

Biosonar signals and cerebellar auditory neurons of the mustached bat.

In the vermis (VIp, VIIa, VIIp, and VIII), crus, and paraflocculus of unanesthetized mustached bats Pteronotus parnellii parnellii, responses of single neurons to acoustic stimuli were studied. The stimuli delivered were constant-frequency (CF) tones, frequency-modulated (FM) sounds, noise bursts (NBs), and sounds similar to the orientation sounds (pulses) of the species and echoes. The effect of ablation of the cerebellar cortex on vocalization was also investigated to explore whether the cerebellum was involved in sound emission. In the cerebellum of the mustached bat, auditory neurons are predominantly tuned to frequencies within the bands between 23 and 30, 55 and 63, or 85 and 94 kHz, which are found in the first, second, and third harmonics of bat's biosonar signals, respectively. The first harmonic is represented in the paraflocculus. The second harmonic is represented in vermis VIp and VIIa and crus I and IIa. The third harmonic is mainly represented in vermis VIIp and crus IIp. Different lobules represent different frequencies, but there is no systematic tonotopic representation in each lobule. The resting frequency of the CF component of the second harmonic (CF2) of the pulse differs among bats. The majority of auditory neurons in vermis VIp and VIIa and crus IIa are tuned to the CF2 frequency of the bat's own pulse. The frequency-tuning curves of cerebellar neurons are broader than those of peripheral neurons, reflected in significantly lower quality factors of Q-10, -30, and -50 dBs. In vermis VIp and VIIa, there are tiny clusters of FM-FM and CF/CF combination-sensitive neurons. They show strong facilitation of responses when two FM or CF sounds are delivered with particular relationships in the frequency, amplitude, and time domains. Because the clusters of these combination-sensitive neurons in the cerebellum are so small, we found no sign of a systematic representation of certain acoustic parameters, unlike that found in the auditory cortex. In vermis VIp and VIIa, there is a large cluster of NB-sensitive neurons that are more sensitive to NBs than to CF tones. The wider the bandwidth of the NBs, the better are the responses of these NB-sensitive neurons. The ablation of the vermis (VIp, VIIa, and VIIp), crus, and paraflocculus increases the variation of the CF frequency of the pulse. The ablation of the crus and paraflocculus causes a clear increase in the variation of CF frequency. The ablation of vermis (VIp, VIIa, and VIIp) has only a small effect on the variation. Any of the above ablations has little effect on the repetition rate of the pulse emission and the duration of pulses.(ABSTRACT TRUNCATED AT 400 WORDS)

Multiple time axes for representation of echo delays in the auditory cortex of the mustached bat.

The properties of the orientation sound (pulse) of the Jamaican mustached bat, Pteronotus parnellii parnellii is the same as the Panamanian mustached bat, P.p. rubiginosus. It consists of four harmonics, each containing a long constant-frequency (CF) component followed by a short frequency-modulated (FM) component. Thus, there are eight components in total: CF1-4 and FM1-4. The combination-sensitive area of the auditory cortex in P.p. parnellii consists of two major divisions (FM-FM and CF/CF areas) as in P.p. rubiginosus. The FM-FM area projects to the dorsal fringe (DF) and other areas. Response latencies of neurons in the DF area are longer than those in the FM-FM area. The distribution of latencies is unimodal for the FM-FM area, but bimodal for the DF area. In this electrophysiological study of the response properties of neurons in the DF and FM-FM areas, our aim was to find out how signal processing might be different between the two areas. Both the FM-FM and DF areas consist of three types of FM-FM combination-sensitive neurons: FM1-FM2, FM1-FM3, and FM1-FM4. They do not respond or respond poorly to pulse alone, echo alone, single CF tones or single FM sounds. But they show strong facilitation of response to the echo when it is delivered with particular delays from the pulse. The essential elements in the pulse-echo pair for facilitation are the FM1 of the pulse and FM2 or FM3 or FM4 of the echo. In both the FM-FM and DF areas, the great majority of neurons show short-lasting facilitation, and other neurons show long-lasting facilitation. FM-FM neurons are tuned to particular echo delays, i.e., target ranges. In both the FM-FM and DF areas, the width of a delay-tuning curve is linearly related to the value of a best delay. There is no sign that processing of range information is more specialized in the DF area than the FM-FM area. In both the FM-FM and DF areas, three types of FM-FM neurons form independent clusters. Along the major axis of each cluster, best delays for facilitative responses of neurons systematically change according to the loci of the neurons. The more posterior the location, the longer the best delay is. Therefore, there are six time (i.e., range) axes in total. The time axis in the DF area is shorter than that in the FM-FM area.(ABSTRACT TRUNCATED AT 400 WORDS)

A deoxyglucose study on auditory responses in the bat Rhinolophus rouxi

Responses in the auditory system of the echolocating bat Rhinolophus rouxi were mapped with [ 3H]deoxyglucose (DG) autoradiography. After unilateral stimulation with the constant frequency component of the individual bat's echolocation call, stimulus-related DG uptake occurred contralaterally in the dorsolateral and the ventromedial parts of the inferior colliculus, in the ventral medial geniculate body and in the contralateral neocortex. Unilateral 50 kHz-stimulation gave rise to a weakly activated lamina in the dorsolateral contralateral inferior colliculus. The distribution of frequency-evoked DG uptake within the inferior colliculus agrees with electrophysiological findings on an acoustic fovea in the auditory pathway of echolocating bats.

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

The frequency-place map of the horseshoe bat cochlea was studied with the horseradish peroxidase (HRP) technique involving focal injections into various, physiologically defined regions of cochlear nucleus (CN). The locations of labeled spiral ganglion cells and their termination sites on inner hair cells of the organ of Corti from injections into CN-regions responsive to different frequencies were analyzed in three dimensional reconstructions of the cochlea. Horseshoe bats from different geographical populations were investigated. They emit orientation cells with constant frequency (CF) components around 77 kHz (Rhinolophus rouxi from Ceylon) and 84 kHz (Rhinolophus rouxi from India) and their auditory systems are sharply tuned to the respective CF-components. The HRP-map shows that in both populations: the frequency range around the CF-component of the echolocation signal is processed in the second half-turn of the cochlea, where basilar membrane (BM) is not thickened, secondary spiral lamina (LSS) is still present and innervation density is maximal; frequencies more than 5 kHz above the CF-component are processed in the first half-turn, where the thickened BM is accompanied by LSS and innervation density is low; frequencies below the spectral content of the orientation call are represented in apical turns showing no morphological specializations. The data demonstrate that the cochlea of horseshoe bats is normalized to the frequency of the individual specific CF-component of the echolocation call. The HRP-map can account for the overrepresentation of neurons sharply tuned to the CF-signal found in the central auditory system. A comparison of the HRP-map with a map derived with the 'swollen nuclei technique' following loud sound exposure (Bruns 1976b) reveals that the latter is shifted towards cochlear base by about 4 mm. This discrepancy warrants a new interpretation of the functional role of specialized morphological structures of the cochlea within the mechanisms giving rise to the exceptionally high frequency selectivity of the auditory system.

Inhibition and level-tolerant frequency tuning in the auditory cortex of the mustached bat.

For echolocation the mustached bat, Pteronotus parnellii, emits complex orientation sounds (pulses), each consisting of four harmonics with long constant-frequency components (CF1-4) followed by short frequency-modulated components (FM1-4). The CF signals are best suited for target detection and measurement of target velocity. The CF/CF area of the auditory cortex of this species contains neurons sensitive to pulse-echo pairs. These CF/CF combination-sensitive neurons extract velocity information from Doppler-shifted echoes. In this study we electrophysiologically investigated the frequency tuning of CF/CF neurons for excitation, facilitation, and inhibition. CF1/CF2 and CF1/CF3 combination-sensitive neurons responded poorly to individual signal elements in pulse-echo pairs but showed strong facilitation of responses to pulse-echo pairs. The essential components in the pairs were CF1 of the pulse and CF2 or CF3 of the echo. In 68% of CF/CF neurons, the frequency-tuning curves for facilitation were extremely sharp for CF2 or CF3 and were "level-tolerant" so that the bandwidths of the tuning curves were less than 5.0% of best frequencies even at high stimulus levels. Facilitative tuning curves for CF1 were level tolerant only in 6% of the neurons studied. CF/CF neurons were specialized for fine analysis of the frequency relationship between two CF sounds regardless of sound pressure levels. Some CF/CF neurons responded to single-tone stimuli. Frequency-tuning curves for excitation (responses to single-tone stimuli) were extremely sharp and level tolerant for CF2 or CF3 in 59% of CF1/CF2 neurons and 70% of CF1/CF3 neurons. Tuning to CF1 was level tolerant in only 9% of these neurons. Sharp level-tolerant tuning may be the neural basis for small difference limens in frequency at high stimulus levels. Sharp level-tolerant tuning curves were sandwiched between broad inhibitory areas. Best frequencies for inhibition were slightly higher or lower than the best frequencies for facilitation and excitation. We thus conclude that sharp level-tolerant tuning curves are produced by inhibition. The extent to which neural sharpening occurred differed among groups of neurons tuned to different frequencies. The more important the frequency analysis of a particular component in biosonar signals, the more pronounced the neural sharpening. This was in addition to the peripheral specialization for fine frequency analysis of that component. The difference in bandwidth or quality factor between the excitatory tuning curves of peripheral neurons and the facilitative and excitatory tuning curves of CF/CF neurons was larger at higher stimulus levels.(ABSTRACT TRUNCATED AT 400 WORDS)

Echolocation sound features processed to provide distance information in the CF/FM bat,Noctilio albiventris: evidence for a gated time window utilizing both CF and FM components

Bats of the speciesNoctilio albiventris, trained to discriminate differences in target distance, emitted pairs of pulses at a rate of 7–10/s, the first a constant frequency (CF) pulse of about 8 ms duration and 75 kHz frequency, followed after about 28 ms by a CF/FM pulse having a 6 ms, 75 kHz CF component that terminates in a 2 ms FM sweep to about 57 kHz.

Echo intensity compensation by echolocating bats

When mounted on a swinging pendulum, mustache bats, Pteronotus p. parnellii, emit ultrasonic pulses as they move toward and away from fixed targets. During forward swings they systematically decrease the intensity of their emitted pulses and during backward swings they increase the intensity. In this way, echo strength is continuously adjusted and apparently optimized for signal analysis. We have called this behavior echo intensity compensation. Pteronotus simultaneously Doppler and echo intensity compensate during forward swings of the pendulum but during backward swings they only echo intensity compensate. Pteronotus can regulate the intensity of both the constant frequency and frequency modulated components of their pulses; this regulation is independent of vestibular cues, pulse repetition rates, pulse durations and pulse-echo intervals.

Evoked acoustic emissions and cochlear microphonics in the mustache bat, Pteronotus parnellii.

In the echolocating bat, Pteronotus parnellii, otoacoustic responses at a frequency of 62 kHz are measurable in the external ear canal during continuous and after transient acoustic stimulation. These responses are interpreted to represent emissions from the cochlea. They can reach an amplitude as large as 70 dB SPL and occur in the frequency range most important for echolocation, namely on the average about 700 Hz above the constant frequency component of the orientation calls. A sharp maximum of the amplitude of cochlear microphonic potentials at about 62 kHz could be correlated with the emission frequency. In one bat an evoked otoacoustic response changed to a spontaneous otoacoustic emission. The frequency and amplitude of the evoked otoacoustic responses reversibly decreased after exposure for 1 min to continuous sounds of more than 85 dB SPL with frequencies of about 2.5-7.5 kHz above the emission frequency. Similar effects occurred during anaesthesia or cooling. A possible relation between the existence of otoacoustic emissions and morphological specializations of the cochlea is discussed.

Discrimination performance and echolocation signal integration requirements for target detection and distance determination in the CF/FM bat,Noctilio albiventris

Bats of the speciesNoctilio albiventris were trained to detect the presence of a target or to discriminate differences in target distance by means of echolocation. During the discrimination trials, the bats emitted pairs of pulses at a rate of 7–10/s. The first was an 8 ms constant frequency (CF) signal at about 75 kHz. This was followed after about 28 ms by a short-constant frequency/ frequency modulated (short-CF/FM) signal composed of a 6 ms CF component at about 75 kHz terminating in a 2 ms FM component sweeping downward to about 57 kHz. There was no apparent difference in the pulse structure or emission pattern used for any of the tasks. The orientation sounds of bats flying in the laboratory and hunting prey under natural conditions follow the same general pattern but differ in interesting ways.

Frequency and amplitude representations in anterior primary auditory cortex of the mustached bat.

The orientation sound emitted by the Panamanian mustached bat, Pteronotus parnellii rubiginosus, consists of four harmonics. The third harmonic is 6-12 dB weaker than the predominant second harmonic and consists of a long constant-frequency component (CF3) at about 92 kHz and a short frequency-modulated component (FM3) sweeping from about 92 to 74 kHz. Our primary aim is to examine how CF3 and FM3 are represented in a region of the primary auditory cortex anterior to the Doppler-shifted constant-frequency (DSCF) area. Extracellular recordings of neuronal responses from the unanesthetized animal were obtained during free-field stimulation of the ears with pure tones. FM sounds, and signals simulating their orientation sounds and echoes. Response properties of neurons and tonotopic and amplitopic representations were examined in the primary and the anteroventral nonprimary auditory cortex. In the anterior primary auditory cortex, neurons responded strongly to single pure tones but showed no facilitative responses to paired stimuli. Neurons with best frequencies from 110 to 90 kHz were tonotopically organized rostrocaudally, with higher frequencies located more rostrally. Neurons tuned to 92-94 kHz were overpresented, whereas neurons tuned to sound between 64 and 91 kHz were rarely found. Consequently a striking discontinuity in frequency representation from 91 to 64 kHz was found across the anterior DSCF border. Most neurons exhibited monotonic impulse-count functions and responded maximally to sound pressure level (SPL). There were also neurons that responded best to weak sounds but unlike the DSCF area, amplitopic representation was not found. Thus, the DSCF area is quite unique not only in its extensive representation of frequencies in the second harmonic CF component but also in its amplitopic representation. The anteroventral nonprimary auditory cortex consisted of neurons broadly tuned to pure tones between 88 and 99 kHz. Neither tonotopic nor amplitopic representation was observed. Caudal to this area and near the anteroventral border of the DSCF area, a small cluster of FM-FM neurons sensitive to particular echo delays was identified. The responses of these neurons fluctuated significantly during repetitive stimulation.

Neural representation of bisonar information in the auditory cortex of the mustached bat

For echolocation, the mustached bat (Pteronotus parnellii rubiginosus) emits orientation sounds containing up to four harmonics, each of which consists of a long constant-frequency (CF) component followed by a short frequency-modulated (FM) component. The auditory system of this species extracts different types of bisonar information from complex orientation sound and echo pairs and represents these systematically in the separate areas of the cerebral cortex. Nine clusters of combination-sensitive neurons have thus far been found in the auditory cortex. Two of these clusters making up the CF/CF area consist of CF1/CF2 and CF1/CF3 facilitation neurons which are tuned to particular Doppler shifts, i.e., target velocities from 8 to −2 m/s. The remaining seven clusters consist of different types of FM-FM neurons which are tuned to particular echo delays, i.e., target distances. Three of these clusters, making up the FM-FM area, consist of FM1-FM2, FM1-FM3, and FM1-FM4 facilitation neurons. The FM-FM area projects bilaterally to the dorsal fringe (DF) and ventrolateral (VL) areas of the nonprimary auditory cortex. The DF area consists of three clusters of FM-FM facilitation neurons. The VL area contains a small cluster of facilitation neurons that are tuned only to the FM1-FM2 combination. The FM-FM area represents target distances from 7 to 310 era, while the DF area represents these from 14 to 140 cm. [Work supported by 1-R01-NS 17333.]

Resonance raman studies of ‘Blue’ copper proteins

‘Blue’ copper proteins possess intense visible absorption bands at ≅600 nm due to (Cys)S − → Cu(II) charge transfer. The type 1 copper in these proteins also exhibits anomalously low hyperfine splitting in the EPR spectra and high redox potentials. Crystallographic and EXAFS investigations on two simple blue copper proteins, plastocyanin and azurin, have provided fairly detailed pictures on their active site structures. The resonance Raman (RR) spectra of blue copper proteins are remarkably similar to one another; all have three or more strong bands in the 350–450 cm −1 range; all exhibit intensity enhancement by resonance with the ≅600 nm LMCT band; all spectra have two nearly constant frequency components at ≅750 and ≅250 cm −1 which appear to be vibrational modes of the coordinated cysteinate ligand; and, finally, many weaker spectral features are resolvable in high quality spectra (Fig. 1). The complexity of the RR spectra of the type 1 copper sites suggests the vibrational modes of the chromophore in addition to CuS(Cys) stretching must also contribute. Interpretation is complicated by the fact that the principal peaks in the RR spectra are at unprecedently high frequencies for copper complexes involving sulfur and nitrogen coordination. We recently undertook a normal coordinate analysis of the CuN 2S(S′) chromophore structure of Pseudomonas aeruginosa azurin. We found that the anomalously high frequencies can be explained by the shortness of the CuS (cysteinate) bond and the ▪ t001 Raman Frequencies (cm −1) for CuLADH at 77 K. Protein ν a ν b ν c ν d CuLADH 415 350 254 199 + NADH 420 359 263 202 + pyrazole 413 368 246 196 strongly coupled nature of the vibrations. Good agreement with observed azurin frequencies was obtained for a trigonal pyramidal model with Cu(II) coordinated to two histidines and one cysteinate [1]. The structure of the zinc enzyme, liver alcohol dehydrogenase (LADH), is well documented. Substitution of the catalytic zinc by Cu(II) yields a protein that has type 1 copper properties. We have investigated the RR spectrum of this system and find it to be an excellent model for the spectra of blue copper proteins [2]. A spectrum of CuLADH is shown in Fig. 1. The main spectral features are also at high frequencies and correlate well with those observed for azurin. The catalytic Zn(II) ion in LADH is coordinated by two cysteinates, one histidine, and one water molecule in a tetrahedral environment. We attribute the sharp Raman peak at 415 cm −1 in CuLADH to a predominantly Cuhistidine vibration and the broader band at ≅ 350 cm −1 to contributions from the two Cu-cysteinates. The high frequencies of the chromophore vibrations lead to the prediction that the CuS bonds distances in CuLADH are also close to 21.1 Å, as in azurin and plastocyanin. Addition of the coenzyme, NADH, or pyrazole, a competitive inhibitor of alcohol oxidation in the native enzyme, to the copper proteins causes only minor changes in the RR spectrum of the Cu(II) chromophore (Table I). Thus, despite the large shift of the absorbance maximum from 580 to 495 nm upon pyrazole binding, the copper site appears to maintain its near tetrahedral geometry. Since normal coordinate analyses indicate that vibrational frequencies are sensitive to geometric variations in this type of system [1], any structural changes responsible for the altered λ max and hyperfine splitting in the Cu-LADH/pyrazole complex must be fairly subtle ones.

Response characteristics of single units in the inferior colliculus of mustache bats to sinusoidally frequency modulated signals

1. The discharge properties of single units in the inferior colliculus of the mustache bat,Pteronotus parnellii, were evaluated with tone bursts and sinusoidal frequency modulated (SFM) stimuli. The SFM signals were designed to mimic the modulation patterns imposed upon the echoes reflected from the beating wings of flying insects. 2. Two groups of neurons were distinguished on the basis of their best frequencies (BFs). The first group was called the filter neurons and had BFs between 60–64 kHz. These neurons are involved in processing the constant frequency component of the bat's echolocation calls. The second group, or non-filter, neurons, had BFs below 60 kHz, or above 64 kHz. 3. Ninety percent of the filter neurons and 80% of the non-filter neurons responded to SFM signals with discharges that were phase locked to the modulation waveform. However, the two groups of neurons differed markedly in their sensitivity to very low modulation depths. The majority of filter neurons displayed locked discharges to SFM depths as low as ±50 Hz, and some even locked to depths of ±10 Hz, while only two non-filter units (out of 71 tested) locked to depths of ±50 Hz, and none locked to ±10 Hz. 4. Most filter units displayed a marked selectivity, or tuning, for particular modulation depths, rates, and signal intensities. In these tuned or selective units, locking could be evoked only over a fairly narrow range of depths, rates, and/or intensities. When SFM parameters outside of the neuron's tuned range were presented, only phasic-on or on-off discharges could be evoked. 5. The influence of the SFM carrier frequency was also evaluated in filter units. In some units, the particular carrier frequency used was not critical for evoking locked discharges so long as the signal encroached upon the unit's tuning curve. In the majority of filter units, however, there was a marked asymmetry in that some carrier frequencies were much more effective in evoking locked discharges than were other frequencies. In some asymmetric units, frequencies below the BF were most effective and in other units carrier frequencies above the BF were most effective. 6. We examined the inhibitory surround patterns in 15 filter units under the assumption that a predominant inhibitory flank on one or another side of the BF might account for the asymmetry in the effective SFM carrier frequencies. Detailed analyses in eight filter neurons yielded no relationship between the position of the inhibitory side bands and the asymmetry of SFM frequencies evoking locked discharges.

Cochlear microphonic potentials elicited by biosonar signals in flying bats, Pteronotus p. parnellii.

Cochlear microphonic (CM) potentials were recorded from the bat, Pteronotus p. parnellii during tethered flight and during simulated flight on a pendulum. For each emitted signal the frequency of the ca. 61 kHz constant frequency (CF) component was compared with the frequency response characteristics of the animals's ear. The majority of "resting pulses' had CF components with the maximum frequency approximately 200 Hz below the best frequency (BF) of the CM audiogram. Doppler shift compensation occurred only during forward swings of the pendulum and in such a way that the echo CF components were always maintained near the BF, but on the low frequency slope of the CM audiogram. CM responses to emitted pulses were usually small in amplitude and in some animals no responses were seen. Echoes Doppler shifted upward, however, evoked high amplitude potentials. Echo CF components estimated to be at least 43 dB fainter than the emitted pulses evoked higher amplitude CM potentials than the loud emitted pulses. Echoes from large surfaces up to 4.5-5.0 meters away evoked CM potentials as high in amplitude as those elicited by emitted pulses, even when there was no Doppler shift. Beats in the CM were observed on many occasions and occurred as a result of pulse-echo and echo-echo interactions.