Foraging behaviour and echolocation in the rufous horseshoe bat (Rhinolophus rouxi) of Sri Lanka

Summary In October 1984 foraging areas and foraging behaviour of the rufous horseshoe bat, Rhinolophus rouxi, were studied around a nursery colony on the hill slopes of Sri Lanka. The bats only foraged in dense forest and were not found in open woodlands (Fig. 1). This strongly supports the hypothesis that detection of fluttering prey is by pure tone echolocation within or close to echo-cluttering foliage. During a first activity period after sunset for about 30–60 min, the bats mainly caught insects on the wing. This was followed by a period of inactivity for another 60–120 min. Thereafter the bats resumed foraging throughout the night. They mainly alighted on specific twigs and foraged in flycatcher style. Individual bats maintained individual foraging areas of about 20x20 m. They stayed in this area throughout the night and returned to the same area on subsequent nights. Within this area the bats generally alighted on twigs at the same spots. Foraging areas were not defended against intruders. The bats echolocated throughout the night at an average repetition rate of 9.6±1.4 sounds/s. While hanging on twigs they scanned the surrounding area for flying prey by turning their bodies continuously around their legs. On average they performed one brief catching flight every 2 min and immediately returned to one of their favourite vantage points. Echolocation sounds may consist of up to three parts, a brief initial frequency-modulated (FM) component, a long constant frequency (CF) part lasting for about 40–50 ms, and a final FM part again (Fig. 4b, c). Adult males and females emitted pure tone frequencies in separate bands, the males from 73.5–77 kHz and the females from 76.5–79 kHz (Fig. 5). During scanning for prey from vantage points, the bats mostly emitted pure tones without any FM component (Fig. 4a). The last few pure tones emitted before take-off were prolonged to about 60 ms duration. The final FM part was therefore not an obligatory component of the echolocation signals in horseshoe bats. During flight and especially during emergence from the cave, most sounds consisted of a pure tone and loud initial and final FM sweeps. We therefore suggest that the initial FM part might also be relevant for echolocation. From our observations we conclude that the FM components are especially important during obstacle avoidance. In most sounds emitted in the field a fainter first harmonic was present. It was usually up to 30 dB fainter than the second harmonic, but in some instances it was as loud or even distinctly louder than the second one (Fig. 6a). Even within one sound the intensity relationship between the two harmonics may be reversed. We therefore suggest that the first harmonic is an integral part of the signal and relevant for information analysis in echolocation.     

Unusual echolocation behavior in a small molossid bat, <Emphasis Type="Italic">Molossops temminckii,</Emphasis> that forages near background clutter

When searching for flying insects, Molossops temminckii uses unusual echolocation calls characterized by upward modulation of frequency vs time (UFM). Call frequency increases asymptotically in the relatively long (∼8 ms) pulses from a starting frequency of ∼40 kHz to a long narrowband tail at ∼50 kHz. When approaching a prey, the bat progressively increases the duration of calls and intersperses in the sequence broadband downwardly frequency-modulated signals with a terminal frequency of about 53 kHz, which totally replaces the UFM signals at the end of the approach phase. The sequence progresses to a capture buzz resembling those from other molossid and vespertilionid bats. The M. temminckii wing morphology is characterized by an average aspect ratio and a high wing loading, suggesting that it is more maneuverable than the typical Molossidae but less than typical Vespertilionidae. M. temminckii regularly forages near clutter, where it needs to pay attention to the background and might face forward and backward masking of signals. We hypothesize that the UFM echolocation signals of M. temminckii represent an adaptation to foraging near background clutter in a not very maneuverable bat needing a broad attention window. The broadband component of the signal might serve for the perception of the background and the narrowband tail for detection and perhaps classification of prey. Bats may solve the signal masking problems by separating emission and echoes in the frequency domain. The echolocation behavior of M. temminckii may shed light on the evolution of the narrowband frequency analysis echolocation systems adopted by some bats foraging within clutter.     

Echolocation behavior and signal plasticity in the Neotropical bat Myotis nigricans (Schinz, 1821) (Vespertilionidae): a convergent case with European species of Pipistrellus?

We used both field and flight cage observations to investigate the echolocation and foraging behavior of the seldom studied, small, aerial insectivorous bat Myotis nigricans (Vespertilionidae) in Panama. In contrast to its temperate congeners, M. nigricans foraged extensively in open space and showed an echolocation behavior well adapted to this foraging habitat. It broadcast narrowband echolocation signals of 7 ms duration that enhance the chance of prey detection in open space. Because of rhythmical alternations of signal amplitude from signal to signal in our sound recordings of search signals in open space, we conclude that the bats scanned their environment with head movements, thereby enlarging their search volume. In edge-and-gap situations, and in the flight cage, M. nigricans introduced an initial broadband component to its search calls. In the field and in the flight cage, M. nigricans hawked for prey in aerial catches; gleaning was never observed. M. nigricans demonstrates call structures, such as narrow bandwidth and rather long signals adapted to foraging predominantly in open space. Moreover, call structure is highly plastic, allowing M. nigricans to forage in edge-and-gap situations also. These adaptations in call structure and plasticity have evolved convergently at least twice within the genus Myotis. Finally, M. nigricans echolocation and foraging behavior parallels that of the small, aerial, insectivorous pipistrelle bats (Vespertilionidae), which are not closely related to M. nigricans but forage in similar habitats.     

Echolocation,development, and vocal communication in the lesser bulldog bat,Noctilio albiventris

Summary Foraging and echolocation behavior and its ontogeny in the lesser bulldog bat, Noctilio albiventris, were studied in Panama under field and captive conditions. The vocalizations utilized for echolocation and communication were monitored. Adult N. albiventris captured insect prey from the water surface employing various combinations of CF/FM (constant frequency and frequency modulated) signals. The proportions of CF/FM and the repetition rate were a function of the bat's activity. Most adults exhibited post-sunset and pre-dawn foraging activity, although several telemetered lactating females foraged for only the half hour after dusk, spending the rest of the night with their babies in the roost. When the juveniles began to leave the roost at the age of two months, they appeared to accompany their mothers on initial flights.Captive infant Noctilio developed slowly, and did not fly until about 5–6 weeks postnatally. They continued to nurse for almost 3 months, even though they were capable of eating solid food at about 6 weeks. Previous to weaning, mothers fed their infants with masticated food from their cheekpouches.At birth, Noctilio emit a combination of long FM isolation calls and shorter CF/FM pulses. Mothers nurse only their own babies which they appear to recognize by a vocal signature contained in the infants' isolation calls. The individual isolation calls, as well as the mother's communication sounds, appear to be variations of an FM sinusoidal wave. The periodicity and amplitude change, and different portions including harmonics are added or deleted. The short CF/FM signals of the infant evolve into the adult orientation type signals as the CF component increases in frequency and the repetition rate increases. These sounds appear to serve a dual function in communication and echolocation. Mother-young pairs were observed to call antiphonally, utilizing CF/short FM signals in retrieval situations. This duetting was also observed in bats flying over the Chagras River after the time the juveniles began to fly, and may function to maintain vocal contact during initial foraging flights.Deceased     

Echolocation call design and limits on prey size: a case study using the aerial-hawking bat Nyctalus leisleri

The echolocation calls used by Nyctalus leisleri during search phase in open air space are between 9 and 14 ms long, with the peak energy between 24 and 28 kHz. The pulses are shallowly frequency-modulated with or without an initial steep frequency-modulated component. The diet consists primarily of small flies (Diptera), including many chironomids (wingspan 9–12 mm) and yellow dung flies (Scatophaga; wingspan 24 mm), but also of some larger insects such as dung beetles (Coleoptera; Scarabaeoidea), caddis-flies (Trichoptera) and moths (Lepidoptera). The echo target strength of some prey items was measured. Contrary to models based on standard targets such as spheres or disks, the echo strength of real insects was found to be virtually independent of the emitted frequency within the 20–100 kHz frequency range. A model was used to calculate probable detection distances of the prey by the bat. Using narrow-band calls of 13.7 ± 2.7 ms duration, a bat would detect the two smallest size classes of insect at greatest range using calls of 20 kHz. The results may therefore explain why many species of large and medium sized aerial-hawking bats use low-frequency calls and still eat mostly relatively small insects. The data and model challenges the assumption that small prey are unavailable to bats using low-frequency calls.     

The effectiveness of katydid (<Emphasis Type="Italic">Neoconocephalus ensiger</Emphasis>) song cessation as antipredator defence against the gleaning bat <Emphasis Type="Italic">Myotis septentrionalis</Emphasis>

Many nocturnal katydids (Orthoptera: Tettigoniidae) produce intense calling songs, and some bat species use these songs to detect and locate prey. One Nearctic katydid species, Neoconocephalus ensiger, ceases or pauses singing in response to bat echolocation calls. We tested the hypothesis that song cessation is an effective defence against gleaning bats (i.e., bats that take prey from surfaces). We observed Myotis septentrionalis, a sympatric bat species that uses prey-generated sounds when gleaning, attack and feed on singing N. ensiger in an outdoor flight room. These bats demonstrated a preference for the calling song of N. ensiger over a novel cricket calling song when they were broadcast from a speaker in the flight room. Bats attacked speakers broadcasting N. ensiger calling song as long as the song was continuous and aborted their attack if the sound stopped as they approached, regardless of whether a katydid was present as a physical target on the speaker. Echolocation calls were recorded during attacks and no significant differences were found between continuous and interrupted song approaches for four call parameters, suggesting that M. septentrionalis may not use echolocation to locate silent prey. Therefore, song cessation by katydids in response to ultrasound is an effective defence against gleaning bats.     

Foraging behavior and echolocation of wild horseshoe bats Rhinolophus ferrumequinum and R. hipposideros (Chiroptera,Rhinolophidae)

Summary 1. Echolocation and foraging behavior of the horseshoe bats Rhinolophus ferrumequinum and R. hipposideros feeding under natural conditions are described. 2. The calls of both species consisted predominantly of a long CF segment, often initiated and terminated by brief FM sweeps of substantial bandwidth. 3. R. hipposideros typically flew close to vegetation, and fed by aerial hawking, gleaning and by pouncing on prey close to the ground. R. hipposideros called with a CF segment close to 112 kHz which is the second harmonic of the vocalization; its calls included low intensity primary harmonics, and had prominent initial and terminal FM sweeps of considerable bandwidth. When searching for prey on the wing it had longer interpulse intervals than R. ferrumequinum, but emitted shorter pulses at a higher repetition rate; overall it had a similar duty cycle to R. ferrumequinum. 4. R. ferrumequinum, calling with a CF segment close to 83 kHz, also used harmonics other than the dominant secondary in its calls, and modified its echolocation according to ecological conditions. This species showed certain parallels with R. rouxi of Asia. It was observed feeding by aerial hawking and by flycatching. When scanning for prey from a perch (perch hunting), calls were of shorter duration, and interpulse intervals were on average longer, than when bats were flying. Mean duty cycle was longer in flight, and the bandwidths and frequency sweep rates of the FM segments in the calls increased in comparison with perched bats. 5. FM information may facilitate determination of target range and the location and nature of obstacles; it may also be involved in the interpretation of echoes and the detection of moving targets among clutter. The rising FM sweep initiating the call in both species when flying (and to a lesser extent perch hunting) in the wild must have a significant adaptive role, and should be considered an essential component of the call; rhinolophids should be termed FM/CF/FM bats.Abbreviations CF constant frequency - FM frequency modulated - FM₁ initial rising frequency sweep - FM₂ terminal falling frequency sweep - PRR pulse repetition rate - SD standard deviation - SNR signal-to-noise ratio     

Echolocation in two very small bats from Thailand Craseonycteris thonglongyai and Myotis siligorensis

Summary The echolocation and hunting behavior of two very small bats, Craseonycteris thonglongyai (Hill) and Myotis siligorensis (Horsfield), from Thailand, were investigated using multiflash photographs, video, and high-speed tape recordings with a microphone array that allowed determination of distance and direction to the bats. C. thonglongyai is the world's smallest mammal and M. siligorensis is only slightly larger. Both bats hunted insects in open areas. The search signals of C. thonglongyai were 3.5 ms long multiharmonic constant frequency (CF) signals with a prominent second harmonic at 73 kHz repeated at around 22 Hz. The band width (BW) of the short terminal frequency modulated (FM) sweep increased during the very short approach phase. In the final buzz the CF component disappeared, the duration decreased to 0.2 ms, and the repetition rate increased to 215 Hz (Figs. 2, 3, 4). There was no drop in frequency in the buzz. The video recordings of C. thonglongyai indicated that it seizes insects directly with the mouth (Fig. 1). M. siligorensis produced 5.4 ms long CF search signals at 66 kHz. The repetition rate was around 13 Hz. In the approach phase an initial broad band FM sweep was added. The buzz consisted of two phases, buzz I and buzz II. Buzz 11 was characterized by short cry durations (around 0.3 ms), a constant high repetition rate (185 Hz), a distinct drop in frequency, and a prominent second harmonic (Figs. 5, 6, 7). The drop in frequency, apparently typical of vespertilionid bats, has been explained by physiological limitations in sound production. However, C. thonglongyai produced very short signals at very high repetition rates without any frequency drop. The drop may be of adaptive value since it enables M. siligorensis to produce very short signals with high sweep rates. The drop moves the pronounced second harmonic into the frequency range of most interest to the bat (Fig. 7D). The sweep rate in this frequency range may now increase to twice the maximum rate that the vocal cords can produce directly. C. thonglongyai and M. siligorensis belong to different superfamilies, Emballonuroidea and Vespertilionoidea, respectively. In spite of their phylogenetic distance they produce strikingly similar search signals of narrow BW around 70 kHz with high source levels (100–115 dB peSPL peak equivalent sound pressure level). We argue that the signal resemblance is due to the similarity in size and hunting behavior of the two bats both hunting insects in open areas. High frequencies are heavily attenuated in air, but because of their small size the bats are restricted to hunting small insects which only reflect echoes at high frequencies. Thus, the emitted frequency is probably the lowest possible given the prey size. Hence, the two bats can only maximize the range of their sonar by decreasing the BW and emitting high intensities. Correspondence to: A. Surlykke     

The roles of echolocation and olfaction in two Neotropical fruit-eating bats, Carollia perspicillata and C. castanea, feeding on Piper

We studied the echolocation and foraging behavior of two Neotropical frugivorous leaf-nosed bats (Carollia perspicillata, C. castanea: Phyllostomidae) in a flight cage. To test which cues Carollia uses to detect, identify, and localize ripe Piper fruit, their preferred natural food, we conducted experiments under semi-natural conditions with ripe, unripe, and artifical fruits. We first offered the bats ripe fruits and documented their foraging behavior using multiflash stereophotography combined with simultaneous sound recordings. Both species showed a similar, stereotyped foraging pattern. In searchflight, the bats circled through the flight cage in search of a branch with ripe fruit. After finding such a branch, the bats switched to approach behavior, consisting of multiple exploration flights and the final approach when the bats picked up the fruit at its tip and tore it off in flight. Our behavioral experiments revealed that odor plays an important role in enabling Carollia to find ripe fruit. While foraging, Carollia always echolocated and produced multiharmonic, frequency-modulated (FM) signals of broad bandwidth, high frequency, short duration, and low intensity. We discriminated an orientation phase (mostly a single pulse per wingbeat) and an approach phase (groups of two to six pulses per wing beat). We conclude from the bats' behavioral reaction to real and artificial fruit as well as from characteristic patterns in their echolocation behavior that during exploration flights, Carollia changes from primarily odor-oriented detection and initial localization of ripe fruit to a primarily echo-oriented final localization of the position of the fruit. Received: 27 March 1997 / Accepted after revision: 28 February 1998     

Fishing and echolocation behavior of the greater bulldog bat,Noctilio leporinus,in the field

When hunting for fish Noctilio leporinus uses several strategies. In high search flight it flies within 20–50 cm of the water surface and emits groups of two to four echolocation signals, always containing at least one pure constant frequency (CF) pulse and one mixed CF-FM pulse consisting of a CF component which is followed by a frequency-modulated (FM) component. The pure CF signals are the longest, with an average duration of 13.3 ms and a maximum of 17 ms. The CF component of the CF-FM signals averages 8.9 ms, the FM sweeps 3.9 ms. The CF components have frequencies of 52.8–56.2 kHz and the FM components have an average bandwidth of 25.9 kHz. A bat in high search flight reacts to jumping fish with pointed dips at the spot where a fish has broken the surface. As it descends to the water surface the bat shows the typical approach pattern of all bats with decreasing pulse duration and pulse interval. A jumping fish reveals itself by a typical pattern of temporary echo glints, reflected back to the bat from its body and from the water disturbance. In low search flight N. leporinus drops to a height of only 4–10 cm, with body parallel to the water, legs extended straight back and turned slightly downward, and feet cocked somewhat above the line of the legs and poised within 2–4 cm of the water surface. In this situation N. leporinus emits long series of short CF-FM pulses with an average duration of 5.6 ms (CF 3.1 and FM 2.6) and an average pulse interval of 20 ms, indicating that it is looking for targets within a short range. N. leporinus also makes pointed dips during low search flight by rapidly snapping the feet into the water at the spot where it has localized a jumping fish or disturbance. In the random rake mode, N. leporinus drops to the water surface, lowers its feet and drags its claws through the water in relatively straight lines for up to 10m. The echolocation behavior is similar to that of high search flight. This indicates that in this hunting mode N. leporinus is not pursuing specific targets, and that raking is a random or statistical search for surface fishes. When raking, the bat uses two strategies. In directed random rake it rakes through patches of water where fish jumping activity is high. Our interpretation is that the bat detects this activity by echolocation but prefers not to concentrate on a single jumping fish. In the absence of jumping fish, after flying for several minutes without any dips, N. leporinus starts to make very long rakes in areas where it has hunted successfully before (memory-directed random rake). Hunting bats caught a fish approximately once in every 50–200 passes through the hunting area.     

Hunting in unfamiliar space: echolocation in the Indian false vampire bat, Megaderma lyra, when gleaning prey

The literature suggests that in familiar laboratory settings, Indian false vampire bats (Megaderma lyra, family Megadermatidae) locate terrestrial prey with and without emitting echolocation calls in the dark and cease echolocating when simulated moonlit conditions presumably allow the use of vision. More recent laboratory-based research suggests that M. lyra uses echolocation throughout attacks but at emission rates much lower than those of other gleaning bats. We present data from wild-caught bats hunting for and capturing prey in unfamiliar conditions mimicking natural situations. By varying light level and substrate complexity we demonstrated that hunting M. lyra always emit echolocation calls and that emission patterns are the same regardless of light/substrate condition and similar to those of other wild-caught gleaning bats. Therefore, echoic information appears necessary for this species when hunting in unfamiliar situations, while, in the context of past research, echolocation may be supplanted by vision, spatial memory or both in familiar spaces.Communicated by T. Czeschlik     

The echolocation and hunting behavior of Daubenton's bat,Myotis daubentoni

Summary The echolocation and hunting behavior of Daubenton's bat (Myotis daubentoni) were studied in the field under completely natural conditions using a multiflash photographic system synchronized with high-speed tape recordings. The hunting behavior of M. daubentoni is separated into four stages. In the search flight stage Daubenton's bat flies with an average speed of 3.4±0.6 m/s SD usually within 30 cm over water surfaces searching for insects. After the detection of potential prey, the approach flight stage occurs, during which the bat approaches the target in a goal-directed flight. The stage tail down indicates that M. daubentoni is close to the potential prey (approximately 10–22 cm) and is preparing for the catch. The insects are caught with the interfemoral membrane, the feet, and sometimes with the additional aid of a wing. In the stage head down, the bat seizes the prey during flight. Immediately afterwards, Daubenton's bat returns to search flight. M. daubentoni shows the typical echolocation behavior of a vespertilionid bat, emitting frequency-modulated (FM) echolocation signals. The three behavioral stages search, approach, and terminal phase (Griffin et al. 1960) are used to describe the pulse pattern of foraging M. daubentoni in the field. The terminal phase (or buzz) of Daubenton's bat is separated into two parts: buzz I and buzz II. Buzz II is distinguished from buzz I by the following characteristics: a sharp drop in terminal frequency, a distinct reduction in the bandwidth of the first harmonic, a continuous high repetition rate throughout the phase in the range 155–210 Hz, very short pulses (0,25–0.3 ms) and interpulse intervals (4.5–5.0 ms) at the end of the phase, and a distinct decrease in duty cycle. A pause in echolocation separates the end of the terminal phase from the ongoing search phase. The reduction in sound duration after the detection of a target and during pursuits with successfull or attempted catches is discussed in relation to the actual distance of the bat to the target at each stage. It is likely that Daubenton's bat reduces sound duration during approach and terminal phase in order to prevent an overlap of an outgoing pulse with the returning echo from the target. It is argued that the minimum detection distance can be estimated from the sound duration during search flight. Estimates of detection and reaction distances of M. daubentoni based upon synchronized photos and echolocation sequences are given to corroborate this hypothesis. An average detection distance of 128 cm and an average reaction distance of 112 cm were determined. Each behavioral stage of foraging M. daubentoni is characterized by a distinct pattern of echolocation signals and a distinct stage in hunting behavior. The approach flight in hunting behavior coincides with the approach phase and with buzz I in echolocation behavior. The stage tail down corresponds to buzz II. The stage head down is correlated with a pause in echolocation. Immediately afterwards, the bat returns into search flight and into the search phase, emitting search signals.     

Natterer’s bat (Myotis nattereri Kuhl, 1818) hawks for prey close to vegetation using echolocation signals of very broad bandwidth

We present a hitherto unknown prey perception strategy in bats: Myotis nattereri (Vespertilionidae, Chiroptera) is able to perceive prey by echolocation within a few centimeters of echo-cluttering vegetation, by using frequency-modulated search signals of very large bandwidth (up to 135 kHz). We describe the species’ search behavior and echolocation repertoire from the field and from experiments in a flight tent. In the field, bats varied signal parameters in relation to their distance from vegetation and usually flew close to vegetation. In the flight tent, M. nattereri detected and localized prey by echolocation alone as close as 5 cm from vegetation. Apparently, the bats were able to tolerate some overlap between prey and clutter echoes. Passive prey cues (vision, olfaction, prey-generated sounds) were not used in prey perception. The bats selected prey by size. The animals performed aerial catches and produced approach sequences typical for aerial hawking bats, but were able to do so within a few centimeters of the substrate. M. nattereri thus has access to silent, suspended prey very close to vegetation (e.g., spiders, and caterpillars on threads). Received: 29 September 1999 / Received in revised form: 12 February 2000 / Accepted: 12 February 2000     

Fruit detection and discrimination by small fruit-eating bats (Phyllostomidae): echolocation call design and olfaction

We studied the role of echolocation and other sensory cues in two small frugivorous New World leaf-nosed bats (Phyllostomidae: Artibeus watsoni and Vampyressa pusilla) feeding on different types of fig fruit. To test which cues the bats need to find these fruit, we conducted behavioral experiments in a flight cage with ripe and similar-sized figs where we selectively excluded vision, olfaction, and echolocation cues from the bats. In another series of experiments, we tested the discrimination abilities of the bats and presented sets of fruits that differed in ripeness (ripe, unripe), size (small, large), and quality (intact(infested with caterpillars). We monitored the bats' foraging and echolocation behavior simultaneously. In flight, both bat species continuously emitted short (<2 ms), multi-harmonic, and steep frequency-modulated (FM) calls of high frequencies, large bandwidth, and very low amplitude. Foraging behavior of bats was composed of two distinct stages: search or orienting flight followed by approach behavior consisting of exploration flights, multiple approaches of a selected fruit, and final acquisition of ripe figs in flight or in a brief landing. Both bat species continuously emitted echolocation calls. Structure and pattern of signals changed predictably when the bats switched from search or orienting calls to approach calls. We did not record a terminal phase before final acquisition of a fruit, as it is typical for aerial insectivorous bats prior to capture. Both bat species selected ripe over unripe fruit and non-infested over infested fruit. Artibeus watsoni preferred larger over smaller fruit. We conclude from our experiments, that the bats used a combination of odor-guided detection together with echolocation for localization in order to find ripe fruit and to discriminate among them.     

Foraging habitat and echolocation behaviour of Schneider's leafnosed bat, Hipposideros speoris, in a vegetation mosaic in Sri Lanka

The Hipposideridae and Rhinolophidae are closely related families of bats that have similar echolocation (long-duration pure-tone signal, high duty cycle) and auditory systems (Doppler-shift compensation, auditory fovea). Rhinolophid bats are known to forage in highly cluttered areas where they capture fluttering insects, whereas the foraging habitat of hipposiderid bats is not well understood. Compared to rhinolophids, hipposiderid calls are shorter in duration, have lower duty cycles, and they exhibit only partial Doppler-shift compensation. These differences suggest that the foraging habitat of the two families may also differ. We tested this hypothesis by studying foraging and echolocation of Hipposideros speoris at a site with a range of vegetation types. Bats foraged only while in flight and used all available closed and edge habitats, including areas adjacent to open space. Levels of clutter were high in forest and moderate in other foraging areas. Prey capture (n=42) occurred in edge vegetation where it bordered open space. Echolocation signals of H. speoris lacked an initial upward frequency-modulated sweep and were of moderate duration (5.1-8.7 ms). Sequences had high duty cycles (23-41%) and very high pulse repetition rates (22.8-60.6 Hz). Variation in signal parameters during search phase flight across foraging habitats was low. H. speoris showed a greater flexibility in its use of foraging habitat than is known for any rhinolophid species. Our study confirmed that there are differences in habitat use between hipposiderid and rhinolophid bats and we suggest that this divergence is a consequence of differences in their echolocation and auditory systems.     

Flexible bat echolocation: the influence of individual,habitat and conspecifics on sonar signal design

Acoustic signals which are used in animal communication must carry a variety of information and are therefore highly flexible. Echolocation has probably such functions and could prove as flexible. Measurable variabitlity can indicate flexibility in a behaviour. To quantify variability in bat sonar and relate to behavioural and environmental factors, I recorded echolocation calls of Euderma maculatum, Eptesicus fuscus, Lasiurus borealis and L. cinereus while the bats hunted in their natural habitat. I analysed 3390 search phase calls emitted by 16 known and 16 unknown individuals foraging in different environmental and behvioural situations. All four species used mainly multiharmonic signals that showed considerable intra- and inter-individual variability in the five signal variables I analysed (call duration, call interval, highest and lowest frequency and frequency with maximum energy) and also in the shape of the sonagram. A nested multivariate analysis of variance identified the influences of individual, hunting site, close conspecifics and of each observation on the frequency with maximum energy in the calls, and on other variables measured. Individual bats differed in multiple comparisons, most often in the main call frequency and least often in call interval. In a discriminant function analysis with resubstitution, 56–76% of a species' calls were assigned to the correct individual. Distinct individual call patterns were recorded in special situations in all species and the size of foraging areas in forested areas influenced temporal and spectral call structure. Echolocation behaviour was influenced by the presence of conspecifics. When bats were hunting together, call duration decreased and call interval increased in all species, but spectral effects were less pronounced. The role of morphometric differences as the source of individually distinct vocalizations is discussed. I also examined signal adaptations to long range echolocation and the influence of obstacle distance on echolocation call design. My results allow to discuss the problems of echo recognition and jamming avoidance in vespertilionid bats.     

Interindividual use of echolocation calls: Eavesdropping by bats

Summary The use of other individual's echolocation calls by little brown bats, Myotis lucifugus, was tested by observing the response of free-flying bats to presentations of recorded echolocation calls and artificial sounds. Bats responded by approaching conspecific calls while searching for food, night roosts, nursery colonies and mating/hibernation sites. Response was low or non-existant to other sounds. While searching for prey, M. lucifugus also responded to the echolocation calls of Eptesicus fuscus, a sympatric species with overlapping diet but distinctly different echolocation calls. Subadults were especially responsive to conspecific calls.All four situations in which the bats responded involve patchily distributed resources at which bats accumulate. Concentrations of echolocation calls thus likely serve as cues regarding the location of resources. Individuals approaching feeding groups, for example, could increase prey detection range by up to 50 times over individuals relying solely on their own echolocation.Although the costs associated with eavesdropping may be negligible for M. lucifugus, for other species, particularly territorial ones, being conspicuous may be a disadvantage and the possibility of being over-heard by other bats may have been one factor involved in the evolution of echolocation call design.     

Male sperm whale (Physeter macrocephalus) acoustics in a high-latitude habitat: implications for echolocation and communication

Sperm whales (Physeter macrocephalus) are deep-diving predators foraging in meso- and bathypelagic ecosystems off the continental shelves. To investigate the ecophysiological and communicative function of various click types from male sperm whales in a high-latitude habitat, we deployed a large-aperture array of calibrated hydrophones off northern Norway (N69, E15). Data show that sperm whales in this habitat produce three click types: usual clicks, creak clicks and, occasionally, slow clicks. Usual clicks and creak clicks exhibit short duration, profound directionality and a frequency content suited for echolocation on meso- and bathypelagic fish and squids. The acoustic properties and low repetition rate of usual clicks are suited for long-range echolocation, whereas creak clicks have properties equivalent to signals in buzzes, the terminating pulse trains known from echolocating bats during prey capture. From these source parameters and the high acoustic activity during foraging dives, it is concluded that echolocation is an important sensory cue in prey location. Sound pressure levels of creak clicks and usual clicks measured off the acoustic axis suggest that sperm whales may be subjected to eavesdropping by conspecifics, thereby conveying information about food aggregations at estimated ranges of 6 km for creak clicks and 16 km for usual clicks. Slow clicks exhibit low directionality, low-frequency emphasis and a reduced repetition rate, suggesting that this click type is more suited for communication than for echolocation. Slow clicks can be detected by submerged conspecifics at ranges up to 60 km. Thus, sperm whales producing slow clicks may represent an odontocete species that utilizes long-range sound communication.     

Studies on underwater sounds III. On the mechanism of sound production and the underwater sounds produced by Linuparus trigonus

Linuparus trigonus V. Siebold were placed in a tank, with a hydrophone suspended in one corner, in order to investigate the mechanism of sound production and the under-water sounds released. Sounds were recorded by tape recorder and analyzed by means of sound spectrograph. L. trigonus emits creaky sounds by rubbing the protuberance of the antennal coxa against the white tubercle in front of its optic stalk. The protuberance of the coxa molds a hollow, with the opening covered by a thin membrane; this facilitates the production of under-water sounds. However, these sounds are produced only when the antenna is lifted. It is also possible to produce these sounds artificially using dead lobsters. When disturbed by external stimulus, L. trigonus flaps back and accelerates the repitition rate. The under-water sounds produced are a series of pulses, which can be divided into 2 groups: (1) The A type sound; this has a relatively slow repetition rate (10 to 80 times/sec) and is weak at the low frequency range below 3 kHz; the sounds, therefore, are manifested on the sonagram in a pattern consisting of some layers of frequencies which are almost constant. (2) The B type sound; this comprises a series of pulses which are powerful even at low frequency. The repetition rate is very high, and not recognizable on the sonagram.     

Greater spear-nosed bats give group-distinctive calls

Individually distinctive vocalizations are ubiquitous; however, group distinctive calls have rarely been demonstrated. Under some conditions, selection should favor calls indicating social group membership in animals that forage in groups. Greater spear-nosed bats (Phyllostomus hastatus) give calls that appear to facilitate recognition of social group mates who are unrelated. Females give loud broadband (4–18 kHz) vocalizations termed screech calls when departing on foraging trips and at foraging sites. Screech calls help to establish foraging groups among social group members, and to maintain contact over the long distances they travel while foraging. I test two hypotheses about how screech calls may be structured to convey caller identity. Individual calls may be distinct and group members may learn to recognize each individual's calls and to associate the individual with the social group. Alternatively, groups may give distinct calls and individuals within groups may share call characteristics. To test these hypotheses I conducted multivariate acoustic analysis of multiple calls from 28 bats from three social groups. Although the ubiquity of individually distinctive calls in other taxa makes this result more likely, the results reveal that group calls are highly distinctive. Individual bats within groups are statistically indistinguishable. Calls appear to decrease slightly in frequency as bats age. Call convergence among unrelated group mates implies vocal learning in this species. Received: 28 March 1996 / Accepted after revision: 6 October 1996