Individuality in trumpet calls of the crested auklet (<Emphasis Type="Italic">Aethia cristatella</Emphasis>), a highly social species

Crested auklet is a unique representative of the family Alcidae with a complex social behavior nesting in dense colonies with a size of up to one million individuals. Here we study specific individual features in their trumpet calls, loud vocalizations used by auklets as an advertising display. In 2008 and 2009, we recorded 231 calls of 24 individually marked male crested auklets from the Talan Island (Sea of Okhotsk). According to a stepwise discriminant function analysis based on seven variables in the call introduction, the rate of correct call assignment to an individual was 84.8% and that in the case of seven variables of the main part of the call was 82.3%, which considerably exceeds a random classification. Thus, a single introduction or a single main part of the call is sufficient for a reliable individual identification of a calling bird. We assume that such redundancy of information for individual recognition can enhance identification of calls of a large number of auklet conspecifics in dense colonies with a nesting density of several tens of pairs per 1 m².     

Vocal and Optical Indicators of Individual Quality in a Social Seabird,the Crested Auklet (Aethia cristatella)

Indicators of individual quality in ornamentation or in vocalizations have been reported for different animal species. However, no studies have jointly investigated ornamentation and vocalizations in one species. The crested auklet (Aethia cristatella, Alcidae) is a small colonial seabird of the North Pacific and is unusual for a bird in using optical, vocal, and olfactory signals. We estimated the potential for coding individual quality in vocalizations and plumage ornamentation and the relationship between vocal and optical traits in crested auklets. During the summer seasons of 2008–2009, we recorded 359 trumpet calls from 28 individually marked males and measured indices of body size, condition, and plumage patterns of 58 male and 48 female crested auklets from a breeding colony on Talan Island, Sea of Okhotsk. We found strong interindividual differences in trumpet call characteristics. Furthermore, we found that the maximum fundamental frequency of the loudest notes of the trumpet call is negatively correlated with body condition, and head crest length is positively correlated with body size. However, we found no relationship between vocal and ornamental traits. The results suggest that advertising calls of crested auklets signal caller individuality and quality, but future experimental studies should test whether or not this is indeed case.     

Size of ornament is negatively correlated with baseline corticosterone in males of a socially monogamous colonial seabird

The Goymann–Wingfield model predicts that glucocorticoid levels in social animals reflect the costs of acquiring and maintaining social status. The crested auklet is one of the few avian colonial species where a mutual ornament in males and females is used in both sexual and aggressive displays. Previous studies of the crested auklet support the notion that the crest ornament is a badge of status in this species. Here, we examined the relationship between the crest ornament size and the adrenocortical function in breeding crested auklets. Crest length was negatively correlated with corticosterone at baseline in males, but not in females. Baseline corticosterone in females (but not in males) was negatively correlated with body condition index. Although male and female crested auklets are monomorphic in their ornamental traits, our results suggest that the socially mediated physiological costs associated with status signaling may differ between the sexes.     

Behavior of crested auklets (<Emphasis Type="Italic">Aethia cristatella</Emphasis>, Charadriiformes,Alcidae) in the breeding season: Visual and acoustic displays

The crested auklet, a highly social planktivorous bird species of the Northern Pacific, is an important component of marine ecosystems. Although visual and acoustic modalities play a major role in the communication of these birds, the available data on the repertoire of their vocal signals and postures are scarce and lack quantitative analysis. This study deals with visual and acoustic displays of crested auklets on their breeding grounds and the occurrence frequencies of certain forms of social behavior in male and female birds. The data were collected on Talan Island (the Sea of Okhotsk) in 1987–1991 and 2008. They show that the rate of contacts between birds is very high and sex-specific: on average, males initiate 1.13 contacts/min, compared to 0.65 contacts/min initiated by females. Directionality of ruff-sniff displays differs depending on the posture of the recipient bird. The duration of the trumpeting display in males depends on their social surroundings. However, the duration of either the trumpeting display or the mutual cackling display during courtship is independent of the behavioral context. Vocalization of crested auklets is characterized by two independent basic frequencies occurring either sequentially or simultaneously. The role of different communicative modalities in the behavior of the crested auklet is discussed.     

Finding your mate in a seabird colony: contrasting strategies of the Guillemot Uria aalge and King Penguin Aptenodytes patagonicus

Capsule King Penguins recognize their mates by voice, but Guillemots do not need acoustic cues even though their calls show individual variation.

Aims To determine whether the structure of Guillemot calls could allow individual recognition, as with King Penguin, and whether acoustic cues are used to locate mates among a dense mass of conspecifics at a colony.

Methods Observations were made on breeding Guillemots and King Penguins. Calls made by birds returning to their mates were recorded, the signals digitized and the calls analysed. Calls were later played back to the mates of the birds concerned and the effects noted on both them and their neighbours.

Results Both Guillemots and King Penguins emitted calls on return to the breeding site which contained individual signatures and were therefore potentially usable for mate recognition. In King Penguins, auditory recognition was essential for finding a mate, whereas in Guillemots most of the arriving birds located their mate in a dense crowd of conspecifics without the help of acoustic signals. Guillemots could differentiate neighbours from strangers without auditory cues.

Conclusion Calls are essential for the successful identification of mates by King Penguins but not by Guillemots.     

Female collared flycatchers choose neighbouring and older extra‐pair partners from the pool of males around their nests

Extra‐pair copulation is common among passerine birds. Females might engage in this behavior to obtain direct or indirect benefits. They may choose extra‐pair males with larger ornaments, especially if they are costly to produce. Here we studied extra‐pair paternity in the collared flycatcher. Genetic analysis allowed us to identify the presence or absence of extra‐pair young in the focal nests, and to identify extra‐pair fathers. We also identified potential males available as extra‐pair sires around the nests of females who had extra‐pair young. First, we tested the relationship between paternity in own nest and ornament size (wing patch and/or forehead patch), morphological traits and age of social males and females. Second, we compared the same suite of traits among social mates, extra‐pair males and all potential extra‐pair mates. Finally, we investigated the effect of the size of ornaments on the distance between the social nest and that of nest the extra‐pair father. Contrary to our prediction, males with larger ornaments and longer wings lost more paternity in their nests. We also found that early breeders lost less paternity in their nests. Extra‐pair males were older and had longer wings than social and potential extra‐pair males. Females mainly obtained extra‐pair mates near their nests but the distance did not vary according to ornamentation. These results could potentially be explained by differences in mate guarding strategy as older males may be more experienced in guarding their mate and attract other females more easily. More data about mate guarding and prospecting are needed to increase our understanding of mechanisms underlying the extra‐pair paternity in birds.     

Mate recognition by female zebra finch: analysis of individuality in male call and first investigations on female decoding process

Zebra finches are monogamous birds living in large assemblies, which represent a source of confusion for recognition between mates. Because the members of a pair use distance calls to remain in contact, call-based mate recognition is highly probable in this species. Whereas it had been previously demonstrated in males [Vignal, C., Mathevon, N., Mottin, S., 2004. Audience drives male songbird response to mate's voice. Nature 430, 448-451], call-based mate recognition remained to be shown in females. By analysing the acoustic structure of male calls, we investigated the existence of an individual signature and identified the involved acoustic cues. We tested to see if females can identify their mates on the basis of their calls alone, and performed preliminary experiments using modified signals to investigate the acoustic basis of this recognition. Playback tests carried on six individuals showed that a female zebra finch is able to perform the call-based recognition of its mate. Our experiments suggested that the female uses both the energy spectrum and the frequency modulation of the male signal. More experiments are now needed to decipher precisely which acoustic cues are used by females for recognition.     

Social factors affect the singing rates of female northern cardinals Cardinalis cardinalis

Social factors, such as the duration of territorial occupancy or of time paired with a mate can affect the rate at which individual birds sing. This study examined the influence of duration of pair‐bond and territory occupancy as well as date on the rate of singing by male and female northern cardinals Cardinalis cardinalis. When differences in breeding status were controlled, female cardinals sang at higher rates earlier in the season. Females in newly formed pairs sang at significantly higher rates than those in pairs that had previously bred together. In contrast, male cardinals did not show significant variation in the rate of singing throughout the season. The song rates of males in newly formed and established pairs did not differ significantly. Song rates for males and females in mated pairs were not significantly correlated. This study suggests that social factors have a strong effect on the rate at which female cardinals sing. It is possible that increased intra‐sexual aggression by females when they are establishing a new territory with a new mate leads to this higher level of song output. Once females have established a territory and acquired a mate, dear‐enemy effects might diminish the need for acoustic territorial defence. Differences in the constraints of nesting or the attraction of extra‐pair mates might explain the sexual differences in male and female singing behaviour.     

The social organization of a sexually dimorphic honeyeater: the Crescent Honeyeater Phylidonyris pyrrhoptera,at Wilsons Promontory,Victoria

The social organization of the sexually dimorphic and dichromatic Crescent Honeyeater Phylidonyris pyrrhoptera (Latham 1801) was studied at Wilsons Promontory National Park between January 1994 and January 1997. All breeding attempts at one site were followed during the spring and summer of 1996. Most pairs were multibrooded, with pair-bonds maintained throughout the study. Breeding males held well-defined territories. Females, although generally restricting their activities to within their mate’s territory, visited other males’ territories more frequently than did their mates and did so close to the time of egg laying. Males aggressively chased intruding males, but appeared to permit intrusions by non-mate females. Circumstantial evidence suggests some males may kill neighbour’s nestlings. Female Crescent Honeyeaters are solely responsible for nest construction and incubation. While both sexes attended nestlings, males contributed to parental care significantly less than females. Males also provided significantly less parental care than has been reported for monomorphic species of honeyeater. Single syllable calls are given throughout the year. Peaks in the rate of double and multisyllable calls corresponded with peaks in breeding activity. Only males were observed uttering loud multisyllable calls. In contrast to predictions arising from sexual selection theory and observations of the mating system of sexually dimorphic hummingbirds, the population of Crescent Honeyeaters studied exhibited a socially monogamous mating system. However, the very limited male role in parental care and non-observance of male territory boundaries by females suggest the genetic mating system may not be one of monogamy.     

Effects of breeding success, mate fidelity and senescence on breeding dispersal of male and female blue-footed boobies

1. Understanding the effects of individual and population factors on variation in breeding dispersal (the movement of individuals between successive breeding sites) is key to identifying the strategies behind breeders' movements. Dispersal is often influenced by multiple factors and these can be confounded with each other. We used 13 years of data on the locations, mates, breeding success and ages of individuals to tease apart the factors influencing breeding dispersal in a colonially breeding long-lived seabird, the blue-footed booby Sula nebouxii. 2. Breeding dispersal varied among and within years. Males dispersed further in years of higher population density, and late breeding males and females dispersed further than early breeders. This temporal variation related to changes in competition for territory was taken into account in all tests of individual factors influencing breeding dispersal. 3. Individuals that retained their mates from the previous year dispersed shorter distances than those that changed their mates. 4. The effect of previous breeding success depended on mate fidelity. Unsuccessful breeding induced greater dispersal in birds that changed their mates but not in birds that retained their mates, indicating that breeders who change mates may take their own previous breeding experience into account during habitat selection. Faithful individuals may have to stay close to their previous sites to encounter their mates. 5. Male divorcees dispersed over shorter distances than their former mates, possibly because males contribute more than females to establishing territories. 6. Dispersal of males and females declined with increasing age over the first 10-11 years of life, then increased in old age, possibly due to senescent decay in the ability to compete for mates and territories.     

Mating behavior and sex change of the anemonefish,Amphiprion clarkii,in the temperate waters of southern Japan

Synopsis In the main habitat of the anemonefishes Amphiprion, their movements between host sea anemones are generally restricted because of the low population density of hosts and high predation pressures. On the contrary, movements of A. clarkii between hosts were usual in the present study area (temperate waters of southern Japan), where host anemones are abundant. The general social unit of the anemonefishes is an isolated group consisting of a monogamous breeding pair and a varying number of nonbreeders. In the present study area, however, monogamous pairs established territories almost contiguous to others and nonbreeders had home ranges on the outskirts of the pairs' territories. The high host population density allows A. clarkii to move between hosts for searching for mates and acquiring additional mates. Most pair bonds lasted for more than 6 months, but 13% of the pairs separated because of migration of a mate to another territory. Bigamy occasionally originated from a penetration into a territory of a breeder by a mated neighbor of the opposite sex after the former's mate loss. Among 18 males who had lost their mates, only 3 changed sex and others re-paired with immigrant females, migrated to unmated females' territories or invaded pairs' territories. In the present study area, sex change to female is not the best way for an unmated male to increase his future reproductive success because of a loss of time spent on sex change and an opportunity to re-pair with new mates larger than himself, but is adaptively maintained as the best of a bad situation for the unmated male.     

Physiological resonance between mates through calls as possible evidence of empathic processes in songbirds

Physiological resonance – where the physiological state of a subject generates the same state in a perceiver – has been proposed as a proximate mechanism facilitating pro-social behaviours. While mainly described in mammals, state matching in physiology and behaviour could be a phylogenetically shared trait among social vertebrates. Birds show complex social lives and cognitive abilities, and their monogamous pair-bond is a highly coordinated partnership, therefore we hypothesised that birds express state matching between mates. We show that calls of male zebra finches Taeniopygia guttata produced during corticosterone treatment (after oral administration of exogenous corticosterone and during visual separation from the partner) provoke both an increase in corticosterone concentrations and behavioural changes in their female partner compared to control calls (regular calls emitted by the same male during visual separation from the partner only), whereas calls produced during corticosterone treatment by unfamiliar males have no such effect. Irrespective of the caller status (mate/non-mate), calls' acoustic properties were predictive of female corticosterone concentration after playback, but the identity of mate calls was necessary to fully explain female responses. Female responses were unlikely due to a failure of the call-based mate recognition system: in a discrimination task, females perceive calls produced during corticosterone treatment as being more similar to the control calls of the same male than to control calls of other males, even after taking acoustical differences into account. These results constitute the first evidence of physiological resonance solely on acoustic cues in birds, and support the presence of empathic processes.     

Alarm calls of wintering great tits Parus major: warning of mate,reciprocal altruism or a message to the predator?

When a predator is not an immediate threat, a prey may produce relatively loud alarm calls because the risk is low. Since such calls could nevertheless attract acoustically oriented predators, the cost of predator attraction must be outweighed by factors beneficial to the caller. In this field study we elicited low-risk alarm calls by temporarily catching wintering adult male great tits Parus major at feeders both within and outside their territories. We tested whether the alarm calls of dominant males can be explained in terms of mate warning, reciprocal altruism or notifying the predator of detection. If alarms are intended to warn mates, males accompanied by their mates should give alarm calls both within and outside home range, even if other permanent flock members are absent. If alarms are to be explained by reciprocal altruism, male great tits should give low-risk alarm calls when accompanied by permanent flock members other than mate within and not outside of the home-range. If alarm calling is a message to a predator, males should call when foraging alone. We found that male great tits gave low-risk alarm calls when accompanied by their mates, independent of feeder location. They also gave low-risk alarm calls within home ranges in the presence of other permanent flock members when mates were absent. In contrast, only a few males gave calls when foraging alone within their home ranges, or when in the company of unfamiliar great tits outside their usual home-range. The results suggest that the utterance of alarm calls may be explained as mate protection and reciprocal altruism among familiar individuals.     

Sex-specific territorial responses in Tawny Owls Strix aluco

A territorial intruder often poses more of a threat to the territory holder of the same sex as itself. As territorial aggression is associated with costs, aggression shown by birds towards territorial intruders of the opposite sex deserves investigation. This behaviour could arise due to the reproductive value of a mate or through mutualism between members of a pair. We investigated these hypotheses by presenting mated pairs of Tawny Owls Strix aluco with playback of male calls, female calls and a male and female duetting, and recording the number and intensity of responses by the male and female territory holders. Females responded significantly more often to female than to male calls. Males responded equally often to male and female playback. Males which had previously bred successfully with their mate were significantly more likely to respond to female playback in the spring, which suggested males were responding to female playback due to the reproductive value of their mate. There was no evidence of mutualism between members of a pair.     

Vocal buffering of the stress response: exposure to conspecific vocalizations moderates urinary cortisol excretion in isolated marmosets

For many species, the presence of a significant social partner can lessen the behavioral and physiological responses to stressful stimuli. This study examined whether a single, individually specific, signature vocalization (phee call) could attenuate the physiological stress response that is induced in marmosets by housing them in short-term social isolation. Utilizing a repeated-measures design, adult marmosets (n=10) were temporarily isolated from their long-term pair mate and exposed to three conditions: signature vocalizations from the pair mate, phee calls from an unfamiliar opposite sex individual, or no auditory stimuli. Levels of urinary cortisol were monitored as a physiological indicator of the stress response. Urinary cortisol levels were also monitored, while subjects remained undisturbed in their home cages to provide baseline levels. Temporarily isolated marmosets showed significantly higher levels of urinary cortisol than undisturbed marmosets. However, the nature of the acoustic stimulus experienced during isolation led to differences in the excretion of urinary cortisol. Isolated marmosets exposed to a familiar pair mate's vocalization showed significantly lower levels of urinary cortisol than when exposed to unfamiliar marmoset vocalizations (P <0.04) or to no auditory stimuli (P <0.03). Neither the duration of pairing nor the quality of relationship in the pair (indexed by spatial proximity scores) predicted the magnitude of reduction in cortisol in the familiar vocalization condition. The results presented here provide the first evidence that a single, individually specific communication signal can decrease the magnitude of a physiological stress response in a manner analogous to the physical presence of a social partner, a process we term "vocal buffering."     

Age-Related Variation in Mate-Guarding Intensity in the Bluethroat (Luscinia s. svecica)

Female extra‐pair copulations (EPCs) have selected for male paternity guarding strategies in many bird species. In the bluethroat, Luscinia s. svecica, males guard their mates closely during the last 2 d before the start of egg laying, but there is great individual variation in the intensity of mate guarding. Here we show that some of this variation is related to male age. Old males guarded their mates with much lower intensity and sang more than young males, although the latter difference was not statistically significant. Controlling for male age, male and female coloration and size were not significantly related to the intensity of mate guarding. We have previously shown that young and old males had a similar paternity loss in their own broods. On the other hand, old males were far more successful than young males in achieving extra‐pair fertilizations. These patterns suggest that young and old males have different trade‐offs between preventing paternity loss in own nest and gaining paternity in others, because male skills in obtaining EPCs improve with experience and/or because of female preferences for old males as copulation partners. There were no significant relationships between paternity and male mate‐guarding behaviour during the fertile period, indicating that mate guarding is not a very effective paternity‐assurance strategy in the bluethroat.     

Survival, site and mate fidelity in South Polar Skuas Catharacta maccormicki at Anvers Island, Antarctica

In 1974–1975, 34 adult South Polar Skuas Catharacta maccormicki were colour-ringed on 18 nest territories at Bonaparte Point, Anvers Island, near Palmer Station along the Antarctic Peninsula. Subsequently, the area was searched for these birds during the austral summers of 1975–1976 to 1984–1985 and in 1987–1988 and 1989–1990. Fifty-three percent were seen in 1984–1985, 32% in 1987–1988 and 21% in 1989–1990. Annual survival rate averaged 95% from 1974–1975 to 1984–1985; no sexual differences were detected (n = 28 of known sex). Strong territory and mate fidelity were apparent: 34 skuas averaged 1.1 nest territories and 1.7 mates each in 16 years. Only 4 of 34 individuals (all females) were known to change territories, and each territory change involved a change of mates. Although males showed higher territory fidelity than females (P < 0.01), most females (four of five) retained their territories when previous mates failed to return. Seventeen of 34 birds changed mates a total of 24 times; at least 20 mate changes followed the death or disappearance of the former mate. Males showed slightly higher mate fidelity than females (P < 0.04). Female South Polar and Brown Skuas Catharacta lonnbergi did not differ in territory or mate fidelity. From 1974–1975 to 1984–1985, 120 South Polar Skua chicks were ringed on 18 nest territories on Bonaparte Point: 17 were resighted in the Palmer area when they were 3–10 years old. All 15 returnecs were found within 3 km of their natal nest sites, and four of them occupied nest territories on Bonaparte Point.     

Female mate choice based on territory quality in barn swallows

Female mate choice based on territory quality is difficult to study because territories often contain many resources, which are difficult to quantify. Here, using the barn swallow (Hirundo rustica gutturalis) breeding at an outdoor breeding site in Japan, where each male defends only a small territory containing old nests, we studied whether females choose social mates based on territory quality. Since the territories of this species contain few other resources, territory quality can easily be assessed by quantifying old nests in the territory. We made the following four observations: (1) male swallows displayed old nests in their territories to females; (2) the old nests used for the first clutch were less broken than the other old nests within the same territory; (3) territory quality, defined by the number of old nests weighted by the intactness of each old nest, predicted the productivity of the territory; and (4) males with better territories paired with females earlier, and hence bred earlier, than those with inferior territories. The relationships remained significant even after controlling for male morphological traits. Based on these results, we can infer that female swallows choose their mates based, in part, on territory quality.     

Paternal effects on juvenile growth and survival in spring peepers (Hyla crucifer)

Summary In 1986 and 1987 we crossed severalHyla crucifer females to males that obtained mates in nature and to large and small body sized males that did not do so. Offspring resulting from these crosses were raised as pairs of juveniles in 1986, or in isolation in 1987 to assess sire effects on juvenile growth and survival in a competitive and a non-competitive context. When raised as part of a pair of juveniles, individuals sired by natural mates had lower growth rates than their fullsibs raised alone. The reduction in growth was of a similar magnitude whether the cohabiting juvenile was sired by a large or small bachelor. When raised together, individuals sired by natural mates had higher growth rates (indicative of competitive superiority) than their halfsibs sired by large bachelor males, but competed as equals with the progeny of small bachelor males. Progeny of large bachelors competed with progeny of small bachelors as equals. When raised individually in 1987, juveniles sired by natural mates had lower growth rates than their halfsibs sired by bachelor males. Paternal size or mating status had marginally non-significant effects on juvenile survival in 1986 and no effect in 1987. The larger individual in a pair was more likely to survive in 1986. In neither year was juvenile growth rate correlated with prior growth rate as a larva. These experiments suggest that the mating system can affect the distribution of juvenile growth rates (and possible survival rates), and thereby have important fitness consequences long after pair formation. These effects are, however, inconsistent either among sets of individual males or among juvenile environments.     

Why are Male Columbian Ground Squirrels Territorial?

Male territorial defence is a component of many vertebrate mating systems and is often regarded as a tactic for acquiring mates. Traditionally considered within the context of overt site‐specific defence, territoriality actually may have several components which encompass a variety of behavioural tactics (e.g. post‐copulatory mate‐guarding, defence of resources that females need, defence of area around females) that underlie a mating system. The purpose of our study was to evaluate such influences on the territorial behaviour of male Columbian ground squirrels in southwestern Alberta, Canada. Males were dominant and territorial if they defended a minimum convex polygon activity range by chasing other males more within the activity range than they were chased. Subordinate males had no territory and were chased throughout their ranges, but they competed for mates by increasing chases in their activity range when nearby females were oestrous. Dominant males exhibited conditional breeding tactics, tending to chase other dominant males from their territory when nearby females were oestrous, but travelling outside their activity ranges to chase subordinate males when females were not oestrous. Although females mated first with a dominant male on whose territory they resided (and in order from oldest to youngest if several territories overlapped), mating pairs were not exclusive, as females usually mated with additional males. Males also guarded females after copulation and defended females directly just before oestrus, rather than defending territory per se during those times. Thus, males possess a repertoire of behaviours that complement site‐specific territoriality, and territory ownership serves to facilitate a first mating with females that live on the territory.