Hearing in honeybees: operant conditioning and spontaneous reactions to airborne sound

Summary Airborne sound signals emitted by dancing bees (Apis mellifera) play an essential role in the bees' dance communication. It has been shown earlier that bees can learn to respond to airborne sounds in an aversive conditioning paradigm. Here we present a new training paradigm. A Y-choice situation was used to determine the frequency range and amplitude thresholds of hearing in bees. In addition, spontaneous reactions of bees to airborne sound were observed and used to determine thresholds of hearing. Both methods revealed that bees are able to detect sound frequencies up to about 500 Hz. The hearing threshold is 100–300 mm/s peak-to-peak velocity and is roughly constant over the range of detectable frequencies. The amplitude of the signals emitted in the dance language is 5 to 10 times higher, so we can conclude that bees can easily detect the dance sounds.     

Target ranging and the role of time-frequency structure of synthetic echoes in big brown bats,Eptesicus fuscus

Summary Echolocating bats judge the distance to a target on basis of the delay between the emitted cry and the returning echo. In a phantom echo set-up it was investigated how changes in the time-frequency structure of synthetic echoes affect ranging accuracy of big brown bats, Eptesicus fuscus.A one channel phantom target simulator and a Y/N paradigm was used. Five Eptesicus fuscus were trained to discriminate between phantom targets with different virtual distances (delays). The phantom echo was stored in a memory and broadcast from a loudspeaker after a certain delay following the bat's triggering of the system via a trigger microphone. The ranging accuracy was compared using 5 different signals with equal energy as phantom echoes: a standard cry (a natural bat cry), two kinds of noise signals, a high pass, and a low pass filtered version of the standard cry.The standard cry was recorded from one of the bats while judging the distance to a real target. The duration was 1.1 ms, the first harmonic swept down from 55 to 25 kHz and there was energy also in the second and third harmonic. Both noise signals had the same duration, power spectrum, and energy as the standard cry. One noise signal was stored in a memory and hence was exactly the same each time the bat triggered the system. The other variable noise signal was produced by storing the envelope of the standard cry and multiplying on-line with band pass filtered noise. The time-frequency structure (e.g. rise time) of this noise signal changed from triggering to triggering. The filtered signals were produced by either 40 kHz high pass or 40 kHz low pass filtering of the standard cry.The range difference thresholds for the 5 bats were around 1–2 cm (51–119 us) using the standard cry as echo. The range difference threshold with both noise signals was 7–8 cm (around 450 s delay difference). The 40 kHz high pass filtered cry increased the threshold to approximately twice the threshold with the standard cry. With the 40 kHz low pass filtered cry the threshold was increased 2.5–3 times relative to the threshold with the standard cry. A single bat was tested with a signal filtered with a 55 kHz low pass filter leaving the whole first harmonic. The threshold was the same as that with the standard signal.The reduced ranging accuracy with the filtered signals indicates that the full band width of the first harmonic is utilised for ranging by the bats. The substantial reduction in accuracy with the noise signals indicates that not only the full band width but also the orderly time-frequency structure (the FM sweep) of the cry is important for ranging in echolocating bats.Abbreviations FM frequency modulated - CF constant frequency - peSPL peak equivalent sound pressure level - SD standard deviation - SE standard error of mean - EPROM erasable programmable read only memory - FFT fast Fourier transform - S/N signal-to-noise ratio     

Responses and song pattern copying of Omega-type I-neurons in the cricket,Gryllus bimaculatus,at different prothoracic temperatures

Summary Omega-type I-neurons (ON/1) (Fig. 1A) were recorded intracellularly with the prothoracic ganglion kept at temperatures of either 8–9°, or 20–22° or 30–33 °C and the forelegs with the tympanal organs kept at ambient temperature (20–22 °C). The neurons were stimulated with synthetic calling songs (5 kHz carrier frequency) with syllable periods (SP in ms) varying between 20 and 100, presented at sound intensities between 40 and 80 dB SPL. The amplitude and duration of spikes as well as response latency decreased at higher temperatures (Figs. 1 B, 2, 6). At lower prothoracic temperatures (8–9 °C) the neuron's responses to songs with short SP (20 ms) failed to copy single syllables, or with moderate SP (40 ms) copied the syllable with low signal to noise ratio (Fig. 3). The auditory threshold of the ON/1 type neuron, when tested with the song model, was temperature-dependent. At 9° and 20 °C it was between 40 and 50 dB SPL and at 33 °C it was less than 40 dB SPL (Fig. 4). For each SP, the slope of the intensity-response function was positively correlated with temperature, however, at low prothoracic temperatures the slope was lower for songs with shorter SPs (Fig. 5). The poor copying of the syllabic structure of the songs with short SPs at low prothoracic temperatures finds a behavioral correlate because females when tested for phonotaxis on a walking compensator responded best to songs with longer SPs at a similar temperature.Abbreviations epsps excitatory postsynaptic potentials - ON/1 omega-type I-neuron - SP syllable period - SPL sound pressure level     

Frequency and temporal pattern-dependent phonotaxis of crickets (Teleogryllus oceanicus) during tethered flight and compensated walking

Summary Phonotactic responses ofTeleogryllus oceanicus were studied with two methods. Tethered crickets were stimulated with sound while they performed stationary flight, and steering responses were indicated by abdominal movements. Walking crickets tracked a sound source while their translational movements were compensated by a spherical treadmill, and their walking direction and velocity were recorded.During both flight and walking, crickets attempted to locomote towards the sound source when a song model with 5 kHz carrier frequency was broadcast (positive phonotactic response) and away from the source when a song model with 33 kHz carrier frequency was used (negative phonotactic response) (Figs. 2, 4).One-eared crickets attempted, while flying, to steer towards the side of the remaining ear when stimulated with the 5 kHz model, and away from that side in response to the 33 kHz model (Fig. 3). While walking, one-eared crickets circled towards and away from the intact side in response to the 5 kHz and 33 kHz models, respectively (Fig. 6).Positive and negative responses differed in their temporal pattern requirements. Phonotactic responses were not elicited when a non-calling song pattern (2 pulses/s) was played with a carrier frequency appropriate for positive phonotactic responses (5 kHz), but this pattern did elicit negative responses with 33 kHz carrier frequency (Figs. 7–10). When an intermediate carrier frequency, 15 kHz, was used, the response type (positive or negative) depended on the stimulus temporal pattern; the calling song pattern elicited primarily positive responses, while the non-calling song pattern elicited negative responses (Figs. 11, 12, 14, 15). A curious phenomenon was often observed in the flight steering responses; while most responses to 15 kHz song pattern were primarily positive, they often had an initial negative component which was supplanted by the positive component of the response after approximately 2–5 s (Figs. 11, 12).In recent experiments onGryllus campestris, Thorson et al. (1982) described frequency-dependent errors in phonotactic direction (anomalous phonotaxis) and showed how such errors might arise from the frequency-dependent directional properties of the cricket's auditory apparatus. Our findings, particularly the dependence of response type on temporal pattern when 15 kHz carrier frequency was used, argue that frequency-dependent directional properties alone cannot account for positive and negative phonotaxis inT. oceanicus. Rather, these represent qualitatively different attempts to locomote towards and away from the sound source, respectively.We discuss the possibility that central integration of these opposing tendencies might contribute to anomalous phonotaxis.     

Directional hearing in the barn owl (Tyto alba)

Summary The acoustical properties of the external ear of the barn owl (Tyto alba) were studied by measuring sound pressure in the ear canal and outer ear cavity. Under normal conditions, pressure amplification by the external ear reaches about 20 dB between 3–9 kHz but decreases sharply above 10 kHz. The acoustic gain curve of the outer ear cavity alone is close to that of a finite-length exponential horn between 1.2–13 kHz with maximum gain reaching 20 dB between 5–9 kHz. Pressure gain by the facial ruff produces a maximum of 12 dB between 5–8 kHz and decreases rapidly above 9 kHz.The directional sensitivity of the external ear was obtained from pressure measurements in the ear canal. Directivity of the major lobe is explained, to a first approximation, by the sound diffraction properties of a circular aperture. Aperture size is based on the average radius (30 mm) of the open face of the ruff. Above 5 kHz, the external ear becomes highly directional and there is a 26° disparity in elevation between the acoustic axis of the left and right ear. In azimuth, directivity patterns are relocated closer to the midline as frequency increases and the acoustic axis moves at a rate of 20°/octave between 2–13 kHz. Movement of the axis can be explained, to a first approximation, by the acoustical diffraction properties of an obliquely truncated horn, due to the asymmetrical shape of the outer ear cavity.The directional sensitivity of the barn owl ear was studied by recording cochlear microphonic (CM) potentials from the round window membrane. Between 3–9 kHz, CM directivity patterns are clearly different to the directivity patterns of the external ear; CM directionality is abruptly lost above 10 kHz. Above 5 kHz, CM directivity patterns are characterized by an elongated major lobe containing the CM axis, forming a tilted band of high amplitude but low directionality (CM axial plane), closely bordered by minima or nulls. The highest directionality is found in theCM directional plane, approximately perpendicular to the CM axial plane. The left and right ear axial planes are symmetrical about the interaural midline (tilted 12° to the right of the midline of the head) and inclined by an average of 60° to the left and right respectively. In azimuth, the CM axis moves towards the midline at a rate of 37°/octave as frequency increases from 2–9 kHz, crossing into contralateral space near 7 kHz. In the CM directional plane, the directivity of the major lobe suggests that a pressure gradient may occur at the TM. The region of frontal space mapped by movement of the CM axis in azimuth closely matches the angle of sound incidence which would be expected to produce the maximum driving pressure at the TM. It is suggested that acoustical interference at the TM results from sound transmission through the interaural canal and therefore the ear is inherently directional. It is proposed that ear directionality in the barn owl may be explained by the combined effect of sound diffraction by the outer ear cavity and a pressure gradient at the TM.Abbreviations CM cochlear microphonic - RMS root mean square - SPL sound pressure level - TM tympanic membrane     

Simulation of adaptive mechanisms in the vestibulo-ocular reflex

The vestibulo-ocular reflex (VOR), which stabilizes the eyes in space during head movements, can undergo adaptive modification to maintain retinal stability in response to natural or experimental challenges. A number of models and neural sites have been proposed to account for this adaptation but these do not fully explain how the nervous system can detect and correct errors in both gain and phase of the VOR. This paper presents a general error correction algorithm based on the multiplicative combination of three signals (retinal slip velocity, head position, head velocity) directly relevant to processing of the VOR. The algorithm is highly specific, requiring the combination of particular sets of signals to achieve compensation. It is robust, with essentially perfect compensation observed for all gain (0.25X–4.0X) and phase (-180°–+180°) errors tested. Output of the model closely resembles behavioral data from both gain and phase adaptation experiments in a variety of species. Imposing physiological constraints (no negative activation levels or changes in the sign of unit weights) does not alter the effectiveness of the algorithm. These results suggest that the mechanisms implemented in our model correspond to those implemented in the brain of the behaving organism. Predictions concerning the nature of the adaptive process are specific enough to permit experimental verification using electrophysiological techniques. In addition, the model provides a strategy for adaptive control of any first order mechanical system.     

Precedence effect at horizontal and vertical plane and moving lagging signal

The precedence effect refers to the fact that humans are able to localize sound sources in reverberant environments. In this study, sound localization was studied with dual sound source: stationary (lead) and moving (lag) for two planes: horizontal and vertical. Duration of lead and lag signals was 1s. Lead-lag delays ranged from 1-40 ms. Testing was conducted in free field, with broadband noise busts (5-18 kHz). The listeners indicated the perceived location of the lag signal. Results suggest that at delays above to 25 ms in horizontal plane and 40 ms in vertical plane subjects localized correctly the moving signal. At short delays (up to 8-10 ms), regardless of the instructions, all subjects pointed to the trajectory near the lead. The echo threshold varied dramatically across listeners. Mean echo thresholds were 7.3 ms in horizontal plane and 10.1 ms in vertical plane. Statistically significant differences were not observed for two planes [F(1, 5) = 5.52; p = 0.07].     

Comparative collicular tonotopy in two bat species adapted to movement detection,Hipposideros speoris andMegaderma lyra

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 m thick. Within this region, neuronal sheets of about 4–5 m 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 m thickness represent a 1 kHz-band. The largest 1 kHz-slabs (400–600 m) 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 m 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, Q_10dB-values of single units do not exceed 30, whereas inHipposideros speoris units with BFs within the auditory fovea reach Q_10dB-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.Abbreviations BF Best frequency - CF constant frequency - FM frequency modulated - IC inferior colliculus - HS Hipposideros speoris     

Evoked potentials of the auditory cortex of the porpoise,Phocoena phocoena

Summary Evoked potential (EP) recordings in the auditory cortex of the porpoise,Phocoena phocoena, were used to obtain data characterizing the auditory perception of this dolphin. The frequency threshold curves showed that the lowest EP thresholds were within 120–130 kHz. An additional sensitivity peak was observed between 20 and 30 kHz. The minimal EP threshold to noise burst was 3·10^–4–10^/s-3 Pa. The threshold for response to modulations in sound intensity was below 0.5 dB and about 0.1% for frequency modulations. Special attention was paid to the dependence of the auditory cortex EP on the temporal parameters of the acoustic stimuli: sound burst duration, rise time, and repetition rate. The data indicate that the porpoise auditory cortex is adapted to detect ultrasonic, brief, fast rising, and closely spaced sounds like echolocating clicks.Abbreviation EP evoked potential     

Multiple specializations in the peripheral auditory system of the CF-FM bat,Pteronotus parnellii

Summary Cochlear microphonic (CM) and evoked neural potentials (N₁) were recorded from the cochlear aqueduct of awakePteronotus parnellii. The CM audiograms obtained with continuous sounds had more or less uniform thresholds except for a sharp threshold notch at about 60 kHz (Fig. 1). When brief tone bursts were presented, the envelopes of the CM responses were always similar to the envelopes of the applied signals except when tone bursts having frequencies at or close to the frequency of the tuned sensitivity notch were presented (i.e., 59–63 kHz). The CM rise-decay times for frequencies around 60kHz were much longer than those of the presented signals (Fig. 2). The prolonged decay times are thought to be due to the ringing of the basilar membrane resulting from a mechanical resonance in the cochlea.The evoked neural potential audiograms (N₁-on and N₁-off responses) differed considerably from the CM audiogram. Of particular importance is the N₁-off audiogram which exhibited very sharp tuning in four frequency regions: 31–33 kHz, 60–63 kHz, 71–73 kHz, and 91–92 kHz (Fig. 5). The frequencies evoking the lowest thresholds of the CM and N₁-off (in the 60 kHz region) were either identical or differed by only 100–400 Hz.The sharp tuning in the 60 kHz region of both the CM and N₁ audiograms could be eliminated by presenting 90–100 dB continuous sounds for one min but only if the signal frequency was equal to the tuned frequency of the CM audiogram (Figs. 8–13). Presenting intense sounds having frequencies above or below the tuned 60kHz region had no effect on the audiogram. The overstimulation procedure had remarkably specific effects on the CM and N₁-off audiograms causing the greatest threshold increases at the 60 kHz tuned frequency and progressively smaller threshold changes on the slopes of the tuned notch.Assuming that the sharp changes of the N₁-off thresholds reflect some important underlying mechanism, the N₁-off audiograms demonstrate multiple specializations in the peripheral auditory system ofPteronotus with the bat possessing at least three and possibly four sharply tuned regions. With regard to mechanism, the tuned notch in the CM audiogram, the curious CM rise-decay times evoked by tone bursts, and the ease with which the 60 kHz sensitivity notch can be eliminated all argue strongly in favor of a mechanical resonance in the cochlea which is responsible for the sharp tuning around 60 kHz. On the other hand, the absence of tuned notches in the 30 kHz and 90 kHz regions of the CM audiogram together with the absence of any discernable ringing of the CM potentials evoked by 30 kHz and 90 kHz tone bursts both argue against a resonance mechanism for the tuning at these harmonically related frequency regions. Finally, the fact that overstimulating the 60 kHz region had no discernable effect on the N₁-off tuning at 30 kHz and 90 kHz demonstrates that the mechanism responsible for the tuned regions at 30 kHz and 90 kHz are independent of the resonance feature of the cochlea at 60 kHz.Abbreviations BF best frequency - CF constant frequency - CM cochlear microphonics - CM-aft after-response of the CM - FM frequency modulated - N ₁ evoked neural potentials We thank Professor Alvin Novick for the generous support provided during the conduct of these experiments. We also thank Professor Gerhard Neuweiler and Dr. Gerd Schuller for their helpful comments and suggestions. Supported by PHS Grant NB7616 11.     

Response to sound in crickets without tympanal organs (Gryllus campestris L.)

Summary Acoustic signals (10–100 msec, 5kHz, 70 or 80 dB) have an inhibitory effect on chirping in the cricketGryllus campestris L. After a reaction time of approximately 50 msec there is a period of about 150 msec (at 27 °C) during which it is very unlikely that a chirp will begin. The effect is not abolished by removal of the tympanal organs, antennae and cerci. Electrophysiological recordings made from the neck connectives in freely moving insects show that tympanal ablation does not abolish sound reception.     

Parallel processing of proprioceptive information in the terminal abdominal ganglion of the crayfish

The processing of proprioceptive information from the exopodite-endopodite chordotonal organ in the tailfan of the crayfish Procambarus clarkii (Girard) is described. The chordotonal organ monitors relative movements of the exopodite about the endopodite. Displacement of the chordotonal strand elicits a burst of sensory spikes in root 3 of the terminal ganglion which are followed at a short and constant latency by excitatory postsynaptic potentials in interneurones. The afferents make excitatory monosynaptic connections with spiking and nonspiking local interneurones and intersegmental interneurones. No direct connections with motor neurones were found.Individual afferents make divergent patterns of connection onto different classes of interneurone. In turn, interneurones receive convergent inputs from some, but not all, chordotonal afferents. Ascending and spiking local interneurones receive inputs from afferents with velocity thresholds from 2–400°/s, while nonspiking interneurones receive inputs only from afferents with high velocity thresholds (200–400°/s).The reflex effects of chordotonal organ stimulation upon a number of uropod motor neurones are weak. Repetitive stimulation of the chordotonal organ at 850°/s produces a small reduction in the firing frequency of the reductor motor neurone. Injecting depolarizing current into ascending or non-spiking local interneurones that receive direct chordotonal input produces a similar inhibition.     

Effects of Sound Frequency on Audiovisual Integration: An Event-Related Potential Study

A combination of signals across modalities can facilitate sensory perception. The audiovisual facilitative effect strongly depends on the features of the stimulus. Here, we investigated how sound frequency, which is one of basic features of an auditory signal, modulates audiovisual integration. In this study, the task of the participant was to respond to a visual target stimulus by pressing a key while ignoring auditory stimuli, comprising of tones of different frequencies (0.5, 1, 2.5 and 5 kHz). A significant facilitation of reaction times was obtained following audiovisual stimulation, irrespective of whether the task-irrelevant sounds were low or high frequency. Using event-related potential (ERP), audiovisual integration was found over the occipital area for 0.5 kHz auditory stimuli from 190–210 ms, for 1 kHz stimuli from 170–200 ms, for 2.5 kHz stimuli from 140–200 ms, 5 kHz stimuli from 100–200 ms. These findings suggest that a higher frequency sound signal paired with visual stimuli might be early processed or integrated despite the auditory stimuli being task-irrelevant information. Furthermore, audiovisual integration in late latency (300–340 ms) ERPs with fronto-central topography was found for auditory stimuli of lower frequencies (0.5, 1 and 2.5 kHz). Our results confirmed that audiovisual integration is affected by the frequency of an auditory stimulus. Taken together, the neurophysiological results provide unique insight into how the brain processes a multisensory visual signal and auditory stimuli of different frequencies.     

Development of the auditory sensitivity and formation of the acoustically guided defensive behavior in nestlings of the pied flycatcher Ficedula hypoleuca

Age dynamics of generation of the evoked potentials (EP) in the field L of caudal nidopallium (the higher integrative center of the avian auditory system) and development of the auditory-guided defensive behavior were studied in control and visually deprived pied flycatcher Ficedula hypoleuca nestlings. It was shown that the rhythmically organized monofrequency signals with sound frequency 3.5 kHz and higher produced the defensive behavior as the auditory sensitivity to these frequencies matured. After 9 days, the species-specific alarm signal produced more effectively the defensive behavior than the tonal signals. The rhythmically organized sound with filling frequency 0.5 kHz, occupying the less low-frequency diapason than the feeding signal, produced the effect opposite to the alarm signal to increase the nestling mobility. At the initial stage of the defensive behavior development the auditory threshold fell markedly in the frequency diapason corresponding to the frequency diapason of the alarm signal (5–6 kHz), which seemed to facilitate involvement of this diapason signals in the defensive integration. The auditory EP generation thresholds in the whole studied diapason were lower in the visually deprived nestlings than in the normally developing one; however, the ability of the acoustic signals to suppress alimentary reactions fell significantly.     

A sensory map based on velocity threshold of sensory neurones from a chordotonal organ in the tailfan of the crayfish

The central projections of sensory neurones innervating a strand chordotonal organ (CO) in the tailfan of the crayfish, Procambarus clarkii (Girard) have been investigated. The CO monitors movement of the exopodite of the tailfan relative to the endopodite. Intracellular recording and staining were used to characterise the response of the sensory neurones to applied stretches of the chordotonal organ and to reveal their morphology. Two gross morphological types of afferents were found: those that terminated in the terminal (6th) abdominal ganglion on the side ipsilateral to the sensory receptor, and those that had branches in the terminal ganglion and an intersegmental axon that ascended rostrally. Afferents responded to position, velocity and direction of imposed CO displacement. Afferents with particular physiological properties had similar morphologies in different crayfish. Irrespective of their directional responses, afferents had central projection areas dependent upon their velocity thresholds. Many afferents responded only during movement of the CO, and those with the lowest velocity thresholds (2°/s) had branches that projected most anteriorly, while those with progressively higher velocity thresholds (up to 200°/s) projected progressively more posteriorly. Afferents that responded to low velocity ramp movements and spiked tonically projected to more posterior areas of the ganglion than those that responded only to movements.Abbreviations A6SCI sixth abdominal sensory commissure I - CO chordotonal organ - DMT dorsal medial tract - G6 sixth abdominal ganglion - LDT lateral dorsal tract - MDT medial dorsal tract - MVT medial ventral tract - R1–4 nerve roots 1–4 - VLT ventral lateral tract - VMT ventral medial tract     

The precedence effect in the horizontal and vertical planes in experiments with a moving lagging signal

The precedence effect in the localization of a moving lagging sound source was studied in experiments on humans under the free field conditions in the presence of a stationary (lead) sound source. Broad-band noise (5–18 kHz) bursts 1 s in duration presented in the horizontal and vertical planes were used as signals. The lead-lag delays ranged from 1 to 40 ms. The results showed that, if the signals were presented in the horizontal plane, the probability of correct localization of the moving lagging signal was decreased for delays shorter than 25 ms; if the signals were presented in the vertical plane, it was decreased for delays shorter than 40 ms. If the delays were shorter than 8–10 ms, the subjects could not localize the moving lagging signal at all. In this interval of delays, the subjects could localize only the lead signal. The mean echo threshold for signals presented in the horizontal plane was smaller than for signals presented in the vertical plane (7.3 and 10.1 ms, respectively). However, comparison of these values across the sample of subject did not show significant differences [F(1, 5) = 5.52, p = 0.07]. The results of the study suggest that the precedence effect causes a tendency towards a stronger suppression of a moving lagging signal in the vertical plane than in the horizontal plane.     

Biophysics of underwater hearing in the clawed frog,Xenopus laevis

Anesthetized clawed frogs (Xenopus laevis) were stimulated with underwater sound and the tympanic disk vibrations were studied using laser vibrometry. The tympanic disk velocities ranged from 0.01 to 0.5 mm/s (at a sound pressure of 2 Pa) in the frequency range of 0.4–4 kHz and were 20–40 dB higher than those of the surrounding tissue. The frequency response of the disk had two peaks, in the range of 0.6–1.1 kHz and 1.6–2.2 kHz, respectively. The first peak corresponded to the peak vibrations of the body wall overlying the lung. The second peak matched model predictions of the pulsations of the air bubble in the middle ear cavity. Filling the middle ear cavity with water lowered the disk vibrations by 10–30 dB in the frequency range of 0.5–3 kHz.Inflating the lungs shifted the low-frequency peak downwards, but did not change the high-frequency peak. Thus, the disk vibrations in the frequency range of the mating call (main energy at 1.7–1.9 kHz) were mainly caused by pulsations of the air in the middle ear cavity; sound transmission via the lungs was more important at low frequencies (below 1 kHz). Furthermore, the low-frequency peak could be reversibly reduced in amplitude by loading the larynx with metal or tissue glue. This shows that the sound-induced vibrations of the lungs are probably coupled to the middle ear cavities via the larynx. Also, anatomical observations show that the two middle ear cavities and the larynx are connected in an air-filled recess in submerged animals.This arrangement is unique to pipid frogs and may be a structural adaptation to connect all the air spaces of the frog and improve low-frequency underwater hearing. Another function of the recess may be to allow cross-talk between the two middle ear cavities. Thus, the ear might be directional. Our pilot experiments show up to 10 dB difference between ipsi- and contralateral stimulus directions in a narrow frequency range around 2 kHz.     

Cartilage Conduction Is Characterized by Vibrations of the Cartilaginous Portion of the Ear Canal

Cartilage conduction (CC) is a new form of sound transmission which is induced by a transducer being placed on the aural cartilage. Although the conventional forms of sound transmission to the cochlea are classified into air or bone conduction (AC or BC), previous study demonstrates that CC is not classified into AC or BC (Laryngoscope 124: 1214–1219). Next interesting issue is whether CC is a hybrid of AC and BC. Seven volunteers with normal hearing participated in this experiment. The threshold-shifts by water injection in the ear canal were measured. AC, BC, and CC thresholds at 0.5–4 kHz were measured in the 0%-, 40%-, and 80%-water injection conditions. In addition, CC thresholds were also measured for the 20%-, 60%-, 100%-, and overflowing-water injection conditions. The contributions of the vibrations of the cartilaginous portion were evaluated by the threshold-shifts. For AC and BC, the threshold-shifts by the water injection were 22.6–53.3 dB and within 14.9 dB at the frequency of 0.5–4 kHz, respectively. For CC, when the water was filled within the bony portion, the thresholds were elevated to the same degree as AC. When the water was additionally injected to reach the cartilaginous portion, the thresholds at 0.5 and 1 kHz dramatically decreased by 27.4 and 27.5 dB, respectively. In addition, despite blocking AC by the injected water, the CC thresholds in force level were remarkably lower than those for BC. The vibration of the cartilaginous portion contributes to the sound transmission, particularly in the low frequency range. Although the airborne sound is radiated into the ear canal in both BC and CC, the mechanism underlying its generation is different between them. CC generates airborne sound in the canal more efficiently than BC. The current findings suggest that CC is not a hybrid of AC and BC.     

Photosynthetic performance of transplanted ecotypes ofEcklonia cava(Laminariales, Phaeophyta)

Young sporophytes of short-stipe ecotype ofEcklonia cavafrom a warmer locality (Tei, Kochi Pref., southern Japan) and those of long-stipe ecotype from a cooler locality (Nabeta, Shizuoka Pref., central Japan) were transplanted in 1995 to artificial reefs immersed at the habitat of long-stipe ecotype in Nabeta Bay, Shizuoka Pref., central Japan. The characteristics of photosynthesis and respiration of bladelets of the transplanted sporophytes of the two ecotypes were compared in winter and summer 1997; the results were assessed per unit area, per unit chlorophyllacontent and per unit dry weight. In photosynthesis-light curves at 10–29 °C, light saturation occurred at 200–400 mol photon m^–2s^–1in sporophytes from both Tei and Nabeta. The maximum photosynthetic rate (P _max) at 10–29 °C and the light-saturation index (I _k) at 25–29 °C in sporophytes from both localities were generally higher in winter than in summer.P _maxat 25–29 °C (per unit area and chlorophylla) were higher in sporophytes from Tei than those from Nabeta in both seasons. The optimum temperature for photosynthesis was 25 °C in winter and 27 °C in summer at high light intensities of 100–400 mol photon m^–2s^–1. However, at lower light intensities of 12.5–50 mol photon m^–2s^–1, it was 20 °C in winter and 25–27 °C in summer for sporophytes from both locations. Dark respiration increased with temperature rise in the range of 10–29 °C in sporophytes from both locations in summer and winter. The sporophytes transplanted from Tei (warmer area) showed higher photosynthetic activities than those from Nabeta (cooler area) at warmer temperatures even under the same environmental conditions. This indicates that these physiological ecotypes have arisen from genetic differentiation.