Recognition of family-specific calls in stripe-backed wrens

Males of the cooperatively breeding stripe-backed wren Campylorhynchus nuchalis, learn repertoires of stereotyped calls (termed WAY calls) from older male relatives. As a result, these vocalizations are normally specific to patrilineal family groups but are sometimes shared by male relatives in different groups. To determine whether or not this species can recognize the calls of different family groups, I performed playback experiments with individual call types recorded from males of known social and genealogical relationships. Subjects discriminated between the calls of unrelated neighbouring groups and unfamiliar groups, and they discriminated both of these from calls of their own groups. However, subjects failed to distinguish calls of males in other groups from calls of their own groups when these males were members of the same patriline. These results indicate that stripe-backed wrens can discriminate between repertoires of these calls that match or differ from their own. Consequently, they can recognize members of their patriline, not just members of their immediate group. These vocalizations probably provide a useful mechanism for recognizing group membership in this species and might also provide a mechanism for recognizing unfamiliar relatives in other groups. Copyright 1999 The Association for the Study of Animal Behaviour.     

Breeding southern house wrens exhibit a threat-sensitive response when exposed to different predator models

We assessed the ability of southern house wrens (Troglodytes aedon musculus) to recognize and discriminate different birds of prey. We exposed nesting birds to stuffed specimens of two sympatric predator species, the chimango caracara (Milvago chimango, a nest predator) and the roadside hawk (Buteo magnirostris, a predator of adults and nests), and to a dummy of a non-sympatric predator, the double-toothed kite (Harpagus bidentatus, a predator of adults). Nesting wrens avoided going into their nest or took a longer time to resume their parental duties when exposed to the predators than when they were exposed to a control dummy (Chrysomus ruficapillus, a sympatric blackbird). Nest avoidance was higher when birds were exposed to the roadside hawk but no differences were detected when exposed to the chimango caracara or the double-toothed kite. The results indicate that southern house wrens are able to recognize a predator, responding in a graded manner. Our findings support the hypothesis that southern house wrens exhibit a threat-sensitive response during breeding. Also, individuals were able to recognize the unknown predator but failed to correctly assess the threat level represented by it. We propose that correct assessment of threat level by house wrens requires direct experience with the predator, which might mediate in the modulation of the response.     

Learning fine-tunes a specific response of nestlings to the parental alarm calls of their own species

Parent birds often give alarm calls when a predator approaches their nest. However, it is not clear whether these alarms function to warn nestlings, nor is it known whether nestling responses are species-specific. The parental alarms of reed warblers, Acrocephalus scirpaceus ("churr"), dunnocks, Prunella modularis ("tseep"), and robins, Erithacus rubecula ("seee") are very different. Playback experiments revealed that nestlings of all three species ceased begging only in response to conspecific alarm calls. These differences between species in response are not simply a product of differences in raising environment, because when newly hatched dunnocks and robins were cross-fostered to nests of the other two species, they did not develop a response to their foster species' alarms. Instead, they still responded specifically to their own species' alarms. However, their response was less strong than that of nestlings raised normally by their own species. We suggest that, as in song development, a neural template enables nestlings to recognize features of their own species' signals from a background of irrelevant sounds, but learning then fine-tunes the response to reduce recognition errors.     

Behavioral mechanisms preventing filial ovicide in house wrens

Because unmated house wrens (Troglodytes aedon) regularly destroyclutches of conspecifics, we examined mechanisms that preventbreeding individuals from destroying eggs in their own nests.Results of our experimental field study indicate that the egg-destroyingbehavior of males is partially suppressed after mating and thatthe suppression may prevent filial ovicide in some individuals.At least 35% of males continue to destroy conspecific eggs duringthe incubation period of their mates. Because filial ovicideby males is prevented independently of female presence at thenest, we conclude, after eliminating alternative hypotheses,that filial ovicide by males is prevented through their recognitionof nest locations. Egg-destroying behavior of females is alsosuppressed during the incubation. The suppression is strongerthan in males because fewer females than males destroy foreigneggs over a comparable time period. Females respond to experimentallychanged nest location and nest structure, but not egg coloration.We conclude that filial ovicide by females is prevented throughthe suppression of their eggdestroying behavior and throughtheir recognition of nest location and structure.     

A host-race of the cuckoo Cuculus canorus with nestlings attuned to the parental alarm calls of the host species

The common cuckoo has several host-specific races, each with a distinctive egg that tends to match its host's eggs. Here, we show that the host-race specializing on reed warblers also has a host-specific nestling adaptation. In playback experiments, the nestling cuckoos responded specifically to the reed warbler's distinctive 'churr' alarm (given when a predator is near the nest), by reducing begging calls (likely to betray their location) and by displaying their orange-red gape (a preparation for defence). When reed warbler-cuckoos were cross-fostered and raised by two other regular cuckoo hosts (robins or dunnocks), they did not respond to the different alarms of these new foster-parents. Instead, they retained a specific response to reed warbler alarms but, remarkably, increased both calling and gaping. This suggests innate pre-tuning to reed warbler alarms, but with exposure necessary for development of the normal silent gaping response. By contrast, cuckoo chicks of another host-race specializing on redstarts showed no response to either redstart or reed warbler alarms. If host-races are restricted to female cuckoo lineages, then chick-tuning in reed warbler-cuckoos must be under maternal control. Alternatively, some host-races might be cryptic species, not revealed by the neutral genetic markers studied so far.     

Social mating system and reproductive success in house wrens

Current models explaining the establishment and maintenanceof social monogamy and polygyny within avian populations typicallyassume that the reproductive success of polygynous males exceedsthat of monogamous males. This assumption is almost always supportedwhen the number of fledglings or recruits to future breedingpopulations is used to measure adult reproductive success. However,recent studies using DNA markers indicate that simple countsof fledglings or recruits may be a poor estimator of the numberof nestlings sired by the social father. In this paper, we comparethe number of genetic offspring produced by socially monogamousand polygynous house wren (TrogiodyUs atdon) males in nestsat which they were the social father. Polygynous males did,in fact, sire more nestlings in their own nests than did monogamousmales. Moreover, although we have not identified the sires ofextrapair nestlings, we document that even when all extrapairnestlings in this population are hypotheticaOy assigned to monogamousmales, die total reproductive success of polygynous males exceedsthat of monogamous males. These results and those of severalother recent studies are consistent with the assumption thatpolygynous males produce more offspring than monogamous males.     

Evidence for heterozygote instability in microsatellite loci in house wrens

Microsatellite loci have high mutation rates and high levels of allelic variation, but the factors influencing their mutation rate are not well understood. The proposal that heterozygosity may increase mutation rates has profound implications for understanding the evolution of microsatellite loci, but currently has limited empirical support. We examined 20 microsatellite mutations identified in an analysis of 12 260 meiotic events across three loci in two populations of a songbird, the house wren (Troglodytes aedon). We found that for an allele of a given length, mutation was significantly more likely when there was a relatively large difference in size between the allele and its homologue (i.e. a large ‘allele span’). Our results support the proposal of heterozygote instability at microsatellite loci.     

Predation increases acoustic complexity in primate alarm calls

According to most accounts, alarm calling in non-human primates is a biologically hardwired behaviour with signallers having little control over the acoustic structure of their calls. In this study, we compared the alarm calling behaviour of two adjacent populations of Diana monkeys at Taï forest (Ivory Coast) and Tiwai Island (Sierra Leone), which differ significantly in predation pressure. At Taï, monkeys regularly interact with two major predators, crowned eagles and leopards, while at Tiwai, monkeys are only hunted by crowned eagles. We monitored the alarm call responses of adult male Diana monkeys to acoustic predator models. We found no site-specific differences in the types of calls given to eagles, leopards and general disturbances, but there were consistent differences in how callers assembled calls into sequences. At Tiwai, males responded to leopards and general disturbances in the same way, while at Taï, males discriminated by giving call sequences that differed in the number of component calls. Responses to eagles were identical at both sites. We concluded that Diana monkeys are predisposed to use their repertoire in context-specific ways, but that ontogenetic experience determines how individual calls are assembled into meaningful sequences.     

Geographic variability in the alarm calls of the European ground squirrel

Geographic variability in vocalizations has been documented in many mammalian species.We examined to what extent it applies to the alarm calls of the European g...     

Manipulation of offspring sex ratio by second-mated female house wrens

In 1973, Trivers and Willard proposed that offspring sex ratio should be associated with the quality of parental care likely to be provided to the offspring. We tested this hypothesis by comparing fledgling sex ratios in nests of first- and second-mated female house wrens (Troglodytes aedon). In our Wyoming population, second-mated females typically receive little or no male parental assistance and fledge fewer and lower-quality young compared with first-mated females. Assuming that being of lower quality has stronger negative effects on the future reproductive success of males than that of females in this polygynous population, we predicted that fledgling sex ratios in the nests of second-mated females would be female-biased compared with the fledgling sex ratios of first-mated females. Additionally, we asked whether any sex bias at fledging could have resulted from male-biased nestling mortality caused by sex-biased parental provisioning. As predicted, mean fledgling sex ratios in nests of second-mated females were more female-biased than fledgling sex ratios in nests of first-mated females. However, we found no evidence of either sex-biased nestling mortality or sex-biased parental provisioning. These findings suggest that females are responding to their status as second-mated females and to the associated low-quality parental care that their young are likely to receive by producing female-biased clutches rather than manipulating the offspring sex ratio through sex-biased nestling mortality.     

The function of nonlinear phenomena in meerkat alarm calls

Nonlinear vocal phenomena are a ubiquitous feature of human and non-human animal vocalizations. Although we understand how these complex acoustic intrusions are generated, it is not clear whether they function adaptively for the animals producing them. One explanation is that nonlinearities make calls more unpredictable, increasing behavioural responses and ultimately reducing the chances of habituation to these call types. Meerkats (Suricata suricatta) exhibit nonlinear subharmonics in their predator alarm calls. We specifically tested the ‘unpredictability hypothesis’ by playing back naturally occurring nonlinear and linear medium-urgency alarm call bouts. Results indicate that subjects responded more strongly and foraged less after hearing nonlinear alarm calls. We argue that these findings support the unpredictability hypothesis and suggest this is the first study in animals or humans to show that nonlinear vocal phenomena function adaptively.     

Sex ratio manipulation within broods of house wrens, Troglodytes aedon

Trivers & Willard (1973, Science, 179, 90-92) developed an economic theory of parental investment to explain how the relative profitability of sons and daughters varies under specific ecological conditions. In their maternal condition hypothesis they proposed that in polygynous species, the sex of an offspring should be associated with the amount of parental care likely to be made available to it. In these species, the amount of parental investment directed towards offspring may differentially influence the fitness of male and female offspring because males in better than average condition as adults may enjoy larger fitness gains than a female would if she were in better than average condition, while the reverse may be true when conditions are poor. I tested this hypothesis by determining the sex of specific offspring within house wren broods. Because hatching is asynchronous and fledging is synchronous in this polygynous species, last-hatched young fledge having received less parental care than their broodmates. I predicted that last-hatched offspring would be more likely to be female. I found that these young were indeed more likely to be females, were more likely to have hatched from last-laid eggs and were fledging in poor condition relative to their broodmates. I propose that female house wrens behave in a manner consistent with the predictions of the Trivers & Willard hypothesis by producing female offspring last in the laying sequence of their clutches. Copyright 2000 The Association for the Study of Animal Behaviour.     

Microparasite assemblages of conspecific shrew populations in southern California

The microparasite component communities of 2 species of shrews, Notiosorex crawfordi and Sorex ornatus, were investigated for the first time in 2 isolated and 3 continuous landscapes in southern California. With microscopical examination, a total of 6 parasite species was found in N. crawfordi and 8 species in S. ornatus. The highest number (5) of parasite species was detected in the lungs. The corrected estimate of parasite species richness did not significantly correlate with the host abundance in either shrew species. Altitude, and also latitude in N. crawfordi, appeared to be significantly positively associated with the parasite species richness, but this could be due to a false association because of the rare occurrence of some of the parasites or the small altitude range (or both). No other landscape variable analyzed (location, size of the study site, disturbance) was significantly associated with the parasite species richness of the shrews. The parasite assemblages of the 2 shrew species were similar despite the fact that N. crawfordi has a lower metabolic rate than S. ornatus.