Vocalizations by Alaskan moose: female incitation of male aggression

Evidence of female fomentation of male–male aggression as a mechanism of mate choice is rare, especially in mammals. Female choice of mates in polygynous species may be masked by intense male competition or by males attempting to restrict female choice. We studied protest moans of female Alaskan moose Alces alces gigas in interior Alaska, USA, from 1987 to 1990, to determine if moans incited male–male aggression. Alaskan moose exhibit a mating system in which one dominant male (the harem master) herds, defends, courts, and attempts to mate with females in his harem. Protest moans were given by females only in response to courtship. We hypothesized that if protest moans were related to females reducing harassment and exercising mate choice, females should give protest moans more frequently when courted by small males and less often when courted by large males, and that rates of male–male aggression would be elevated following protest moans. Harems were composed of one large male, with a mean of 4.4 females (median = 3 females); 10% of 132 harems included ≥10 females. The temporal pattern of protest moans from late August through November was associated with, but tended to lag behind, mating behavior. The rate of protest moans given by females decreased with increasing size of males courting them. Male–male aggression was significantly less during periods without protest moans than during periods in which protest moans occurred. These results indicate that female moose gave protest moans to reduce harassment by smaller males, and assure a mating opportunity with the most dominant male. Such a subtle mechanism of indirect mate choice by females may occur in other vertebrates in which choice is limited by a mating system in which male–male combat and male dominance over females reduces opportunities for female choice. The importance of female choice may be undervalued in studies of sexual selection in mammals.     

Vocalizations of the North Atlantic pilot whale (Globicephala melas) as related to behavioral contexts

Summary Vocalizations of free-ranging North Atlantic pilot whales were studied in different behavioral contexts to gain insight into the function and biological significance of different sound types. Simple whistles (with no frequency inflections) were heard more frequently when whales were milling, a restful behavior type. During surface active behavior, energetic, often coordinated activity probably representing feeding, many sound types, especially complex whistles (with more frequency inflections) and pulsed sounds, occurred with greater frequency than when this behavior was absent. Greater numbers of most whistle types were produced when whales were spread over a larger area and when more subgroups were present. Thus, in pilot whales, there is a significant relationship between their sounds and their behavior, with vocalizations possibly serving to maintain contact and coordinate movements of the herd. Offprint requests to: L.S. Weilgart at the current address     

Responses of wintering humpback whales (Megaptera novaeangliae) to playback of recordings of winter and summer vocalizations and of synthetic sound

Summary Three natural sounds and one synthetic sound were played back to humpback whales during their 1985 and 1986 winter residency in Hawaiian waters. Playback was conducted from a vessel positioned within visual range of an elevated shorestation equipped with a high-precision surveyor's theodolite, used to determine the positions and movements of observed whale and of the playback vessel. A playback session consisted of 20 min of pretest observation with the vessel in place and underwater speaker deployed, followed by a 20-min test phase during which sound, or a blank tape control, was introduced. A total of 143 playback sessions, involving a total of 338 pods (a single whale or a group of whales), were completed over the two winter seasons. The major response observed during playback was a rapid approach to the playback vessel, characterized in some cases by velocities up to 9 km/h and approaches to within 50 m or less. Whales approaching were mainly singletons and, secondly, apparent adult pairs. No cow-calf pair ever approached. The approach was selective: 21.6% of targeted pods approached in response to a feeding sound recorded in summer feeding grounds in Alaska; 8.3% approached in response to social sounds recorded in the Hawaiian winter grounds in the presence of large surface-active pods; 3.4% responded to playback of winter song; and 4.1% responded to playback of synthetic sound. There were no approach responses to the blank tape control. Singing whales have been identified as males by many researchers. Data from Alaska suggested that the feeding sound was produced by a female; data from Hawaii suggests that the social sounds were produced by males. The different rates of response were attributed to the behavior of sexually active males seeking to affiliate with sexually mature females. Although a female may be present in pods producing social sounds, the presence of multiple males exhibiting aggression may inhibit the approach of other males. Song did not serve as an attractant for females, as measured by direct approach, but may still serve as a basis for female choice.     

Interactions between singing Hawaiian humpback whales and conspecifics nearby

Summary Interactions of singing humpback whales, Megaptera novaeangliae, with conspecifics nearly were studied during the breeding season off the west coast of Maui, Hawaii. On 35 occasions singing humpbacks were followed by boats (Table 1). The movement patterns of these singing whales and other conspecifics nearby were recorded by observers on land using a theodolite.Thirteen of 35 singers stopped singing and joined with nonsinging whales either simultaneously or within a few minutes after ceasing to sing. Another 15 also stopped singing while under observation and were not seen to join with another whale, but all singing whales that joined with other whales stopped singing. Singing whales often pursue nonsinging whales, while nonsinging whales usually turn away from singers (Figs. 4, 5).When a singer joined with a female and calf unaccompanied by another adult, behavior tentatively associated with courtship and mating was observed (Fig. 7). Such behavior also occurred during several interactions between singers and individuals of unknown sex. Aggressive behavior was observed during three interactions between singers and individuals of unknown sex (Fig. 4) and it predominated whenever more than one adult accompanied a cow and calf. During the other occasions when a singer joined another whale, we could not determine the nature of the interaction. Many times the singers and joiner would surface together only once and would then separate. However, on several occasions the singer and joiner would remain together for as long as we could follow them, up to 1.5 h.The roles of singer and joiner can be interchangeable. For instance, on two occasions a singer joined with a whale that either had been singing or started singing later in the day (Fig. 3). Furthermore, on several occasions, a nonsinging whale appeared to displace the singer. Individual singing humpbacks are not strictly territorial, although singers appear to avoid other singers.As the breeding season progressed, singers sang for longer periods of time (Fig. 2). In addition, the probability of a whale joining with the singer decreased by 42% from the first half of the observation period to the second half. Furthermore, this increase in duration of song bouts occurred during that section of the season when female reproductive activity as measured by rate of ovulation is reported to be decreasing in other areas.Our observations support the hypothesis that humpback song plays a reproductive role similar to that of bird song. Humpbacks sing only during the breeding season. If, as seems likely, most singing humpbacks are male, then singing humpbacks probably communicate their species, sex, location, readiness to mate with females, and readiness to engage in agonistic behavior with other whales.     

Group-specific dialects and geographical variation in coda repertoire in South Pacific sperm whales

Codas, which are patterned series of clicks, were recorded from female and immature sperm whales (Physeter macrocephalus) in a number of locations around the South Pacific Ocean and in the Caribbean Sea. Using K-means cluster analysis, 3,644 codas were categorized based on the number of clicks and their patterning. There were 30 resulting types of coda. The numbers of codas of the different types recorded were used to construct repertoires for each recording session, day, group of whales, place, area, and ocean. Strong group-specific dialects, which seem to persist over periods of years, were apparent, overlaid on weaker geographical variation. Significant differences in repertoire were found between the Caribbean and the Pacific Ocean. Sperm whales now join killer whales (Orcinus orca) as the only cetacean species in which dialects (differences in vocal repertoire among neighboring, potentially interacting groups) have been found. Received: 13 June 1996 / Accepted after revision: 19 January 1997     

Vocal and visual stimuli enabling copulation behavior in female buntings

Summary The loud and elaborate songs of male songbirds are throught to serve in territorial defense and to stimulate reproductive behavior in the female. We report here that in contrast to several other species, song alone is inadequate to induce sexual (lordosis) behavior in female indigo and lazuli buntings (Passerina cyanea and P. amoena); they require a more elaborate stimulus configuration to develop the full expression of sexual receptivity as indicated by a stereotyped copulation solicitation display. A live male must be present near the female, singing must ensue, and in addition a second and unique vocal utterance must be heard by the female; this is a soft buzzy-sounding vocalization, audible for no more than a few meters, not recognized previously as a critical arousal signal of the male songbird repertoire. Females also utter similar soft sounds in an intimate vocal exchange with the male leading to solicitation of copulation.     

The song of the humpback whale Megaptera novaeangliae in the West Indies

Songs of the humpback whale Megaptera novaeangliae were recorded and analyzed from Grand Turks in the Bahamas to Venezuela. The design features of the song are as follows. The basic song evolves through a series of different sounds in a fixed order. The song is produced only in the winter tropical calving grounds, just before the whales arrive on the banks. Redundancy is high in that syllables, motifs, phrases and the entire song are repeated. Low, intermediate, and high-frequency sounds are scattered throughout the song. One sound is associated with blowing. The song appears to be partially different each year and there are some differences within a year between banks which may indicate that dialects are present. It is suggested that songs from other populations are quite different. The apparent yearly changes do not occur at one point in time. Only single individuals produce the song and they are hypothesized to be young, sexually mature males. The implications of these various design features are discussed.     

Sighting characteristics and photo-identification of Cuvier’s beaked whales (<Emphasis Type="Italic">Ziphius cavirostris</Emphasis>) near San Clemente Island,California: a key area for beaked whales and the military?

The relationship between beaked whales and certain anthropogenic sounds remains poorly understood and of great interest. Although Cuvier’s beaked whales (Ziphius cavirostris) are widely distributed, little is known of their behavior and population structure throughout much of their range. We conducted a series of five combined visual-acoustic marine mammal surveys from 2006 to 2008 in the southern San Nicolas Basin, a site of frequent naval activity off the southern California coast, west of San Clemente Island. The study area was defined by a 1,800 km² array of 88 bottom-mounted hydrophones at depths up to 1,850 m. The array was used to vector visual observers toward vocalizing marine mammal species. Thirty-seven groups of Cuvier’s beaked whales were encountered during the study period. The overall encounter rate was one group for every 21.0 h of survey effort, and was as high as one group per 10.2 h of effort during the October 2007 survey. Whales were encountered in the deepest portion of the study area, at a mean bottom depth of 1,580 m (SD 138). The average group size was 3.8 individuals (SD 2.4), which was higher than has been reported from other studies of this species. Twenty-four groups were observed over multiple surfacings (median = 4 surfacings, range 2–15). The mean encounter duration of extended sightings was 104 min (SD 98, range 12–466 min) and the mean distance moved over the course of sightings was 1.66 km (SD 1.56, range 0.08–6.65 km). Temporal surfacing patterns during extended encounters were similar to dive behavior described from Cuvier’s beaked whales carrying time-depth recording tags. Seventy-eight photographic identifications were made of 58 unique individuals, for an overall resighting rate of 0.26. Whales were sighted on up to 4 days, with duration from first to last sighting spanning 2–79 days. For those whales sighted on subsequent days, the mean distance between subsequent sightings was 8.6 km (SD 7.9). Individuals resighted over 2–3 days were usually in association with previous group members. Approximately one-third of groups contained more than one adult male, and many of the repeated associations involved adult males. These observations suggest the basin west of San Clemente Island may be an important region for Cuvier’s beaked whales, and also one which affords an unusual opportunity to collect detailed data on this species. Given its status as an active military range, it can also provide the ability to monitor the behavior of individuals in the presence of naval sonar, a critical step in the management of this and other beaked whale populations worldwide.     

Lack of population subdivision among the minke whales (Balaenoptera acutorostrata) from Icelandic and Norwegian waters based on mitochondrial DNA sequences

The minke whale (Balaenoptera acutorostrata) is subject to commercial whaling, but stock identification and assessment are still uncertain. Mitochondrial DNA (mtDNA) sequences were determined to examine the population structure of minke whales from the central and northeastern parts of the North Atlantic, as well as the Antarctic regions IV and V. The analyses include 345 nucleotide positions of the control region of 110 individuals, and 250 nucleotide positions of the NADH dehydrogenase subunit 2 gene for a representative selection of North Atlantic minke whales. Maximum parsimony analyses and sequence divergence calculations did not reveal any genetic differentiation between individuals from the central and northeastern parts of the North Atlantic. These results do not support the International Whaling Commission's separation of minke whales in this area into different management units, and they are in conflict with previously reported results from allozyme analyses. Comparison of minke whale control region sequences showed that the sequence diversity of North Atlantic minke whales is substantially lower (0.0065) than that of Antarctic minke whales (0.0166), and clearly demonstrated that individuals from these two areas represent genetically distinct populations.     

Contrasting C and N isotope ratios from sperm whale skin and squid between the Gulf of Mexico and Gulf of California: effect of habitat

To investigate feeding variation between populations of an apex oceanic predator, stable isotope ratios of carbon (δ¹³C) and nitrogen (δ¹⁵N) have been compared in skin of female and immature male sperm whales (Physeter macrocephalus) from the northern Gulf of Mexico (GoM) and the Gulf of California (GC). Whale sexes were determined genetically. The δ¹³C and δ¹⁵N values from squid muscle were used from the GC, and from inshore and offshore sites in the GoM. We documented contrastingly lower δ¹³C and δ¹⁵N from whales and squid of the GoM compared with those from the GC. While this difference may be associated with variation in trophic position, geographic variation in biochemical cycling influenced significantly the contrasting isotope values between gulfs. Within the northern GoM, the highly distinct δ¹⁵N values of neritic squid versus mesopelagic squid provide further evidence of habitat specificity in δ¹⁵N.     

Patterns of the electric organ discharge during courtship and spawning in the mormyrid fish,Pollimyrus isidori

Summary Pollimyrus isidori's electric organ discharge (EOD) is of the pulse type. Patterns of EOD intervals were investigated prior to, during and following spawning behaviors as related with overt behaviors, and with the sound production by the nestbuilding male. Prior to the time of reproduction, isolated and socially interacting fish (n=15) showed characteristic discharge interval patterns for resting, swimming, probing, hovering and hiding activities. Males (n=8) and females (n=6) did not differ in their mean EOD repetition rates during resting (11.6±2.5 Hz), nor Short Bursts/min (less than 20 intervals of 8–13 ms). In interacting fish Long Bursts (greater than 20 intervals of 8–13 ms, lasting for more than 300 ms) were observed only during the attack and bite sequence. A pursuing fish displayed a rapid alternation of Long Bursts with Discharge Breaks (300–1000 ms silence) during the chase behavior. Avoidance behavior which followed from several attacks was correlated with a Medium Uniform Rate (8–12 Hz) normally lasting for 20 to 60 s, or a Discharge Arrest (silence greater than 1 s) in the submissive fish. The nocturnal courtship behavior began soon after dark (1900 h). Spawning typically started 2 to 5 h after dark, continuing for 2 to 6 h until about 0200 h. During courtship and spawning the female's brief visits (15–25 s) to the male's territory recurred every 30–60 s. At all other times the female was aggressively excluded from the nest region. Courtship and spawning behaviors are described along with the electrical displays identified from 19 spawnings in three fish pairs (from a total of 37 spawnings in 4 males and 4 females). Just prior to the onset of courtship behavior, with male territorial aggression beginning to decline, females switched from a Medium Sporadic Rate pattern (resting and hiding patterns; 13 Hz) to a Medium Uniform Rate pattern (6–8 Hz) while still in their hiding area. Females continued to display this uniform rate throughout the courship and spawning period, including the courtship and spawning bouts when Discharge Breaks or Arrests also occurred. This persistance distinguishes the courtship pattern from the similar avoidance pattern (see above). The male courtship and spawning EOD pattern was similar to the female's and unique for a territorial male. He switched from a High Sporadic Rate (swimming EOD pattern; about 18 Hz) to a regularized Medium Uniform Rate (about 9 to 11 Hz) only during courtship and spawning bouts, including 1–3 EOD Breaks during Vent-to-Vent coupling (average interval: 272±71 ms, n=37). No sooner had the female left the spawning site than he resumed displaying a High Sporadic Rate. This temporal correlation of reproductive behaviors with electrical displays suggests their instrumental role in mutual acceptance of mates. Males showed their sex-specific type of EOD phase-locking, the Preferred Latency Response, only during the first few hours of entry of a fish in their tank. Two females with EOD waveform features more typical of males also spawned repeatedly; waveform does not appear to be critical. Males stopped their nocturnal sound production for the later part of courtship and the whole spawning period. Except for infrequent attacks on the female between spawning bouts, the male did not resume singing until the end of spawning when all eggs were shed (around 0200 h); from this time on the male sang until dawn. The sequencing of the three acoustic elements (moans, grunts, growls) are described. A catalogue of discharge patterns correlated with overt behaviors (Tables 1, 2), and an integrated summary time table of P. isidori's complex reproductive behavior are presented.     

Social organization of female sperm whales and their offspring: constant companions and casual acquaintances

Summary Associations among female sperm whales, Physeter macrocephalus, and their dependent offspring, off the Galapagos Islands were studied between 1985 and 1989. The whales were found in groups containing about 23 individuals, with each individual having approximately 12 constant (over years) companions. These permanent units associated with one another for periods of 6.5 days, although the rate and duration of these associations seemed to vary between years, perhaps because of differences in the food supply. The principal function of the closed units may be care of the offspring, and units in the same general area may derive benefit from feeding in a coordinated manner.Offprint requests to: H. Whitehead     

Chilean Blue Whales as a Case Study to Illustrate Methods to Estimate Abundance and Evaluate Conservation Status of Rare Species

Abstract: Often abundance of rare species cannot be estimated with conventional design‐based methods, so we illustrate with a population of blue whales (Balaenoptera musculus) a spatial model‐based method to estimate abundance. We analyzed data from line‐transect surveys of blue whales off the coast of Chile, where the population was hunted to low levels. Field protocols allowed deviation from planned track lines to collect identification photographs and tissue samples for genetic analyses, which resulted in an ad hoc sampling design with increased effort in areas of higher densities. Thus, we used spatial modeling methods to estimate abundance. Spatial models are increasingly being used to analyze data from surveys of marine, aquatic, and terrestrial species, but estimation of uncertainty from such models is often problematic. We developed a new, broadly applicable variance estimator that showed there were likely 303 whales (95% CI 176–625) in the study area. The survey did not span the whales' entire range, so this is a minimum estimate. We estimated current minimum abundance relative to pre‐exploitation abundance (i.e., status) with a population dynamics model that incorporated our minimum abundance estimate, likely population growth rates from a meta‐analysis of rates of increase in large baleen whales, and two alternative assumptions about historic catches. From this model, we estimated that the population was at a minimum of 9.5% (95% CI 4.9–18.0%) of pre‐exploitation levels in 1998 under one catch assumption and 7.2% (CI 3.7–13.7%) of pre‐exploitation levels under the other. Thus, although Chilean blue whales are probably still at a small fraction of pre‐exploitation abundance, even these minimum abundance estimates demonstrate that their status is better than that of Antarctic blue whales, which are still <1% of pre‐exploitation population size. We anticipate our methods will be broadly applicable in aquatic and terrestrial surveys for rarely encountered species, especially when the surveys are intended to maximize encounter rates and estimate abundance.     

Postcopulatory mate guarding by vocalization in the Formosan squirrel

The Formosan squirrel, Callosciurus erythraeus thaiwanensis, emitted different vocalizations in response to terrestrial and aerial predators and snakes. Each vocalization caused nearby individuals to adopt a different type of anti-predator behaviour. In mating bouts, males produced two types of loud calls: precopulatory calls, emitted before copulations, and postcopulatory calls, emitted after copulations. The latter continued for 17 min on average. The estrous female and other males attending the mating bouts stopped moving during the postcopulatory call, so that the calling male was able to tend the female without interruption. The sound characteristics of anti-terrestrial-predator and postcopulatory calls recorded in the captivity were compared, and none of the ten characters of duration and frequency measured differed between the two calls. Playback experiments also showed that responses to the sounds in two different contexts, escape behaviour and defensive immobility, did not differ. The similarity between anti-predator and postcopulatory calls is discussed with reference to the possibility of manipulation and other explanatory hypotheses.     

Bi-directional sex change in a coral-dwelling goby

Bi-directional sex change has recently been reported among obligate coral-dwelling gobies of the genus Gobiodon. However, neither the functional role of this pattern of sex change nor the frequency of sex change in either direction in natural populations is known. We investigated the social structure and pattern of sex change of Gobiodon histrio at Lizard Island on the Great Barrier Reef. The social structure of G. histrio within coral colonies usually consisted of a single juvenile or a heterosexual adult pair. The size of adult social groups was not constrained by coral colony size. In contrast to expectations for pair-forming species, G.␣histrio was primarily a protogynous hermaphrodite. All immature G. histrio were females and sex change from female to male occurred readily when two mature females were placed in a coral colony. In addition, male G. histrio were able to change back to females when two mature males were placed in a coral. Sex change from female to male, however, occurred with over twice the frequency of sex change from male to female. Where two males were placed in a coral colony, heterosexual pairs were most frequently re-established by immigration of females from outside the treatment population. This pattern might be predicted if sex change from male to female is more expensive than sex change from female to male for G. histrio. Where sex change is expensive, movement may be favoured over sex change, particularly where coral densities are high and movement among corals incurs little mortality risk. Received: 10 November 1997 / Accepted after revision: 16 May 1998     

Effect of food location and quality on recruitment sounds and success in two stingless bees,<Emphasis Type="Italic"> Melipona mandacaia</Emphasis> and<Emphasis Type="Italic"> Melipona bicolor</Emphasis>

It is unclear whether stingless bees in the genus Melipona (Hymenoptera, Apidae, Meliponini) can reliably encode the distance to a food source through recruitment sounds produced inside the nest, in part because the sound features correlated with distance also vary with food quality. We therefore trained marked foragers of two species, Melipona mandacaia and M. bicolor, to feeders at different distances and to different sucrose concentrations at the same distance. In both species, foragers successfully recruited to a rich 2.5-m food source and produced pulsed recruitment sounds in which pulse duration was significantly and positively correlated with distance to the rich food source. When returning from poorer food sources (0.6–1.5 m), foragers of both species decreased sound production, producing shorter sound pulses and longer sound interpulses than they did for 2.5 m food located at the same distance. Thus the temporal structure of M. mandacaia and M. bicolor recruitment sounds varies with distance and food quality. However, nestmates were not recruited by performances for poorer food sources (0.6–1.5 m), whose sucrose concentration was sufficiently low to affect recruitment sounds. Surprisingly, the interphase (the time between behavioral phases that communicate location) also increases with decreasing food quality in the closely related honeybees (Apis), suggesting a potential homology in the effect of food quality on the recruitment systems of Apis and Melipona. We explore the evolutionary implications of these similarities.Communicated by M. Giurfa     

Whistle communication in mammal-eating killer whales (Orcinus orca): further evidence for acoustic divergence between ecotypes

Public signaling plays an important role in territorial and sexual displays in animals; however, in certain situations, it is advantageous to keep signaling private to prevent eavesdropping by unintended receivers. In the northeastern Pacific, two populations of killer whales (Orcinus orca), fish-eating “resident” killer whales and mammal-eating “transient” killer whales, share the same habitat. Previous studies have shown that residents use whistles as private signals during close-range communication, where they probably serve to coordinate behavioral interactions. Here, we investigated the whistling behavior of mammal-eating killer whales, and, based on divergent social structures and social behaviors between residents and transients, we predicted to find differences in both whistle usage and whistle parameters. Our results show that, like resident killer whales, transients produce both variable and stereotyped whistles. However, clear differences in whistle parameters between ecotypes show that the whistle repertoire of mammal-eating killer whales is clearly distinct from and less complex than that of fish-eating killer whales. Furthermore, mammal-eating killer whales only produce whistles during “milling after kill” and “surface-active” behaviors, but are almost completely silent during all other activities. Nonetheless, whistles of transient killer whales may still serve a role similar to that of resident killer whales. Mammal-eating killer whales seem to be under strong selection to keep their communication private from potential prey (whose hearing ranges overlap with that of killer whales), and they appear to accomplish this mainly by restricting vocal activity rather than by changes in whistle parameters.     

Male Scudderia pistillata katydids defend their acoustic duet against eavesdroppers

Acoustic duets—in which the female reveals herself to the advertising male—are a common means of establishing a temporary, pre-mating pair bond within Phaneropterinae katydids. Such duets, however, are especially susceptible to eavesdropping males that orient to signaling females and interrupt the established duet. It would therefore be advantageous for an advertising male to protect his investment in a duet from eavesdroppers. Male Scudderia pistillata katydids produce acoustic advertisement calls after which a conspecific female enters the duet by responding during a specific time-window with her own call, one or more acoustic ticks. We demonstrate here that when a duet is occurring in the presence of other calling males, the focal male produces a single acoustic tick that has a spectrum similar to that of the female’s tick and occurs during the time-window in which the female would respond to his advertisement call within the duet. The male acoustic tick may confound eavesdropping males if they have difficulty performing accurate phonotaxis to a female sound source when sounds arrive from two locations. We tested this hypothesis in laboratory arenas and determined that silent males eavesdrop on advertising male’s duets and accurately locate his female. Moreover, we found that the added acoustic tick produced by advertising males serves to mimic the female response and reduces the accuracy of eavesdropping males to localize the female. Therefore, male ticks appear to act as a form of pre-copulatory acoustic mate guarding of the calling male’s temporary pair bond with the female.     

The effect of ambient temperature on forager sound production and thoracic temperature in the stingless bee, <Emphasis Type="Italic">Melipona panamica</Emphasis>

Foragers of the stingless bees genus Melipona may produce intranidal sounds that are correlated with food location and quality. In this study, we provide the first detailed analysis of pulsed sounds produced by Melipona panamica foragers while feeding on a carbohydrate food source. We trained foragers to a 2.5-M sucrose feeder under normal, ambient temperature (23–33°C) and lower temperature (11–25°C) conditions. We recorded forager sounds under both conditions and tested the effect of temperature of the thorax, feeder plate, and air on sound temporal characteristics. Forager energetic expenditure and the number of pulses per visit were significantly higher in the cold condition than in the normal condition. Foragers spent a longer time at the feeder under the cold condition than during the normal condition. Interpulse durations were significantly shorter in the cold condition than in the normal condition and became progressively and significantly shorter at the end of each performance. Thus, pulse production increased before departure. Foragers increased their thoracic temperatures above ambient at all experimental air temperatures. Under chilled conditions, foragers had a significantly greater difference between thorax temperature and ambient air temperature than under normal conditions. Foragers must achieve a minimum flight muscle temperature before take-off, and thus forager sounds may be linked to muscle warm-up.     

Distribution and diversity of mtDNA lineages among southern right whales (Eubalaena australis) from Australia and New Zealand

Using a biopsy dart system, samples of skin tissue were collected from southern right whales (Eubalaena australis) in 1995 on two wintering grounds, southwest Australia (n = 20) and the Auckland Islands of New Zealand (n = 20); and on offshore feeding grounds at Latitudes 40 to 43°, south of Western Australia (n = 5). A variable section of the mitochondrial DNA control-region (289 nucleotides) was amplified and sequenced from these 45 individuals (21 males, 20 females and 4 of unknown sex), distinguishing a total of seven unique sequences (i.e. mtDNA haplotypes). Two haplotypes were found on both wintering grounds (including a common type representing 45% of each sample), and five types were unique to only one wintering ground. An analysis of variance adapted for molecular information revealed significant genetic differentiation between the two wintering grounds (p = 0.017). The feeding-ground sample was too small for statistical comparison with the wintering grounds, but included two haplotypes found only in the Auckland Islands as well as the common haplotype found on both wintering grounds. The nucleotide diversity and differentiation of mtDNA among the right whales was similar to that among humpback whales (Megaptera novaeangliae) from the same regions (Baker et al. 1998), but haplotype diversity was significantly reduced, perhaps as a result of more intensive hunting during the last century and continued illegal hunting during this century. Received: 16 March 1998 / Accepted: 18 December 1998