Duetting and mate-guarding in Australian magpie-larks (Grallina cyanoleuca)

A recently favored hypothesis is that duetting in birds has a mate-guarding function: a male responds vocally to his partner’s song, thereby forming a duet that repels males who are attracted to her song. Previous studies have not provided unambiguous tests of the mate-guarding hypothesis because: (1) the probability of a male answering his partner’s song has not been shown to increase specifically when the female is fertile, and (2) the probability of a male answering his partner’s song has not been assessed separately from simply a higher song initiation rate. We investigated extra-pair paternity, mate-guarding, and duetting in the socially monogamous Australian magpie-lark (Grallina cyanoleuca). DNA fingerprinting revealed that 3% of young were the result of extra-pair paternity, and we found that males guarded fertile females by staying close to them. However, males did not initiate songs at a higher rate when females were fertile and actually reduced their probability of replying to female song during this period. We conclude that although male magpie-larks did guard fertile females in an attempt to prevent extra-pair copulations, they did not use duetting for this purpose. Received: 10 May 1999 / Received in revised form: 27 September 1999 / Accepted: 2 October 1999     

Do male plumage and song characteristics influence female off-territory forays and paternity in the hooded warbler?

Extra-pair fertilizations are common in many socially monogamous species, and paternity studies have indicated that females may use male vocal performance and plumage ornaments as cues to assess male quality. Female off-territory forays may represent a key component of female choice and male extra-pair mating success, and female foray behaviour is expected to be strongly influenced by indictors of male quality. In this study, we examined how male song and ornamentation affect how often females left their territories, which males they visited and extra-pair paternity in a socially monogamous passerine, the hooded warbler (Wilsonia citrina). We radiotracked 17 females during the fertile period and quantified male vocal performance (song output and rate) and plumage characteristics (size of the black melanin hood and colour of the black hood, yellow cheeks and breast areas). We obtained blood samples and determined paternity at 35 nests including those of 14 females that we radiotracked. Eleven (65%) of the 17 females forayed off-territory, whilst fertile and female foray rate was positively correlated with the number of extra-pair young in the nest. Females that left their territories more frequently were paired with males that sang at a low rate. In addition, extra-pair mates had higher song rates than the social mates they cuckolded (5.3 songs/min vs. 4.4 songs/min). Female off-territory forays or extra-pair paternity were not significantly related to male plumage characteristics. Our results indicate that a high song rate influences both the foray behaviour of a male’s social mate and the likelihood that he will sire extra-pair offspring with neighbouring females.     

Breeding synchrony and paternity in the barn swallow (Hirundo rustica)

The barn swallow (Hirundo rustica) is a socially monogamous passerine which usually breeds in colonies where extra-pair copulations are frequent. Males intensively guard their mates during the female fertile period. Since males are more likely to be available for extra-pair copulations when their mate is not fertile, synchrony in timing of breeding may affect paternity of individual males. In this study, we analysed the change in mate-guarding rate by males in relation to the fertility condition of the female, and the relationships between breeding synchrony and density with paternity in first broods of 52 male barn swallows. Paternity (proportion of nestlings fathered in own brood) was assessed by typing of three highly polymorphic microsatellite loci. Mate guarding by males peaked during the fertile period of their mates. Paternity increased as breeding synchrony in the colony increased. Paternity of barn swallows is positively associated with the degree of exaggeration of male tail ornaments. The relationship between male ornamentation and paternity was partly mediated by an effect of ornament size on breeding synchrony. We suggest that females might delay breeding with low-quality males to enhance their opportunities for being fertilised by high-quality extra-pair males. Received: 16 January 1998 / Accepted after revision: 25 October 1998     

Mixed reproductive strategy and mate guarding in a semi-colonial passerine,the swallow Hirundo rustica

Summary Both male and female swallows Hirundo rustica have a mixed reproductive strategy (parental care for offspring and extra-pair couplations). Mate guarding protects females from male harassment and male swallows from being cuckolded. Females hide their fertile period by copulating successfully with their mates for an extended period during first clutches. Males guard in the pre-fertile period, when many unpaired males are present. Early breeding swallows guard more than late breeders since more sexual chases of females by non-mate males take place in the early period. Solitarily breeding females experience few chases by strange males; copulation frequency, length of copulation period and mate guarding is adjusted to a lower level than among colonial birds. Male guarding activity is more intense in the fertile than in the pre-fertile period. Guarding reduces success of extra-pair copulation attempts.Three female swallows each paired and copulated with a single male and later changed to a new male before starting to breed. Extra-pair copulations most often take place between neighbouring swallows in the fertile period of the female. Many old, early breeding males and many young, late breeding females participate in extra-pair couplations. Successful extra-pair copulations peak in the fertile period contrary to success of pair copulations which does not change during the copulation period.     

Non-aggressive mate guarding by the blue-footed booby: a balance of female and male control

Thirteen pairs of blue-footed boobies (Sula nebouxii) were observed on their colony. Pairs courted frequently and, on average, copulated 24 times during the 30 days before laying, with 38% of those copulations occurring in the last 5 days (presumed fertile period). Males and females increased attendance at the nest site as laying approached. Seven females performed an average seven extra-pair copulations, with 1–2 paired male neighbors, but these were less concentrated in the presumed fertile period than within-pair copulations, and the last two copulations of all 7 females were with their social mates. Rates of female extra-pair copulations were six times lower when their social mate was present, and during the presumed fertile period, no female performed an extra-pair copulation in the presence of her mate. Males did not respond to infidelity of social mates with aggression, prompt copulation, retaliatory copulation, or increase in copulation. Seven of 13 males performed an average of five extra-pair copulations, with 1–3 paired female neighbors, before their own mates began egg-laying. The males' extra-pair copulations represented only 4% of their total copulations during their own mates' presumed fertile periods. Females, the larger sex, apparently control sexual access and copulate with extra males to achieve extra-pair fertilization. Males pursue a mixed strategy: they copulate with extra females, mostly outside their own mate's presumed fertile period, and they copulate increasingly with their social mate as laying approaches, probably assuring some paternity by mate guarding, involving attendance and courtship. Behavior of males and females is also consistent with other hypotheses for extensive joint nest site attendance: pairbonding, copulation access, and territory acquisition. Received: 14 November 1997 / Accepted after revision: 16 May 1998     

Seasonal variation in the duetting behaviour of rufous-and-white wrens (<Emphasis Type="Italic">Thryothorus rufalbus</Emphasis>)

Seasonal variation in animal signalling behaviour has been well documented and has contributed much to our understanding of male signals. In contrast, we know little about seasonal variation in female signals or signals produced jointly by males and females, such as the vocal duets of birds. Here, we examine how singing behaviour changes in relation to time of year and breeding stage in rufous-and-white wrens (Thryothorus rufalbus), neotropical songbirds where both males and females sing and where breeding partners coordinate songs to produce vocal duets. We recorded a colour-marked population of birds over an extended time period encompassing multiple breeding stages. Across all time frames and breeding stages, males sang at higher rates than females and male solos were more common than duets or female solos. Males and females showed divergent seasonal patterns of singing. Females sang more often early in the year, during the pre-breeding season, and female song tapered off as the breeding season progressed. Duetting followed a parallel pattern, which resulted from females showing less duet responsiveness to their partner’s songs later in the year. Male independent song rate peaked at the onset of the rainy season – a time when females become fertile – and males showed the highest level of duet responsiveness during this period. Our results suggest that early in the year, duets appear to be cooperative displays, functioning in joint territory defence and/or the coordination of breeding activities. When females are fertile, however, increased duet responsiveness by males is consistent with mate or paternity guarding.     

Condition-dependent control of paternity by female purple martins: implications for coloniality

Proposed causal links between extra-pair copulation (EPC) and colony formation in socially monogamous birds hinge on the question of which sex controls fertilizations. We examined in colonial purple martins Progne subis (1) whether EPCs were forced or accepted by females, and (2) the degree to which apparently receptive females were able to obtain EPCs against their mates’ paternity defenses. Paternity analyses of multilocus DNA fingerprinting confirmed previous findings of a marked relationship between age class and extra-pair fertilizations (EPFs), with young males losing paternity of 43% (n = 53) of their putative offspring compared to 4% (n = 85) by old males. All assignable extra-pair offspring were sired by old males, with one male obtaining most EPFs each year. Contrary to the hypothesis that EPCs are forced, EPF frequency within age class did not increase with seasonal increases in the number of males per fertile female. Whereas the male control hypothesis predicted that the male age class that mate-guarded more would be cuckolded less, the reverse was true: young males guarded significantly more intensely. The male age class difference in cuckoldry could not be explained by the possibility that young and inexperienced females (which are usually paired to young males) were more vulnerable to forced copulation because EPFs were unrelated to female age. These findings suggest that females (1) pair with old males and avoid EPCs, or (2) pursue a mixed mating strategy of pairing with young males and accepting EPCs from old males. The receptivity to EPCs by females paired to young males put them in conflict with their mates. Two factors determined the paternity achieved by young males: (1) the relative size of the male to the female, with young males achieving much higher paternity when they were larger than their mates, and (2) the intensity of mate-guarding. Both variables together explained 77% of the variance in paternity and are each aspects of male-female conflict. Given female receptivity to EPCs, mate-guarding can be viewed as male interference with female mating strategies. We conclude that EPCs are rarely or never forced, but the opportunity for females paired to young males to obtain EPCs is relative to the ability of their mates to prevent them from encountering other males. Evidence of mixed mating strategies by females, combined with other features of the martin mating system, is consistent with the female-driven “hidden lek hypothesis” of colony formation which predicts that males are drawn to colonies when females seek extra-pair copulations. Received: 23 March 1995/Accepted after revision: 14 January 1996     

Song rates of dark-eyed juncos do not increase when females are fertile

Frequency of singing by birds may vary with reproductive stage in ways that reflect variation in the functions of song in intersexual and intrasexual communication. In dark-eyed juncos (Junco hyemalis) high-amplitude song is produced only by males. To investigate the function of this song, we tested whether fertility of females affected singing by their mates or by neighboring males. Using focal observations, song censuses, and radiotracking data, we determined whether song production varied between and among periods when females were fertile and non-fertile. Our findings show that males do not increase song production when their mates are fertile, nor do they increase song production when neighboring females are fertile. These results suggest that male juncos do not signal their intent to defend territories (or mates) more when females are fertile and that they do not use song to advertise to specific potential participants in extra-pair fertilizations. Received: 13 February 1997 / Accepted after revison: 2 May 1997     

Sexual behavior is related to badge size in the house sparrow Passer domesticus

Summary Badge size, which functions as a signal of dominance status in male house sparrows Passer domesticus, was significantly related to their sexual behavior. Males with large badges participated in communal displays (multi-male chases directed towards single females) more often than males with small badges, irrespective of whether the female involved was the male's mate or not. Experimentally released females were more often chased if they were fertile than if they were nonfertile. Estradiol-implanted females were chased more often than control females without a hormone implant, and males with large badges chased estradiol-implanted females more often than did males with small badges. Both forced extra-pair copulations during communal displays and unforced extra-pair copulations were more often achieved by males with large than small badges. Male house sparrows with large badges also copulated with their mates at a higher rate than did males with small badges. A higher certainty of paternity therefore is hypothetized to accrue to male house sparrows with large badges.     

Female control of offspring paternity in a western population of red-winged blackbirds (Agelaius phoeniceus)

Extra-pair copulations, which occur when individuals that have formed social relationships to breed copulate outside their pairbond, now are recognized as an important component of reproductive success in many species. In situations where both males and females benefit from extra-pair copulations without incurring much risk, an inevitable conflict arises between pairbonded mates. In this study I investigated the conflict of interest between male and female reproductive strategies in a western population of red-winged blackbirds (Agelaius phoeniceus). Female red wings in this population initiate extra-pair copulations, which resulted in a 35% rate of extra-pair fertilization. Females initiated the majority (78%) of extra-pair copulations away from their nesting territory where pairbonded individuals typically copulate, and females that engaged in extra-pair copulations spent a significantly greater amount of time off the marsh during peak fertilization compared to females that did not. In addition, females that nested in areas with a large number of potential extra-pair partners produced significantly more extra-pair fertilized young compared to females that nested on marshes with few male neighbors. Males’ strategies to protect paternity were limited primarily to patrolling territory boundaries and to opportunistically preventing extra-pair copulations off the marsh when they were visible. In this population females appear to use behavioral means to control nestling paternity, which in turn directly affected their mate’s reproductive success, and males were restricted to using strategies that were largely ineffective at preventing the threat of extra-pair paternity. Received: 23 December 1994/Accepted after revision: 17 December 1995     

Extra-pair paternity and tail ornamentation in the barn swallow Hirundo rustica

Females of socially monogamous species may copulate with attractive non-mates to obtain access to the genes of such males, and a preference for attractive copulation partners may result in sexual selection. Extra-pair copulations are common in the socially monogamous barn swallow Hirundorustica, and a 2-year study of paternity using multi-locus DNA fingerprinting demonstrated that 33% of 63 broods and 28% of 261 offspring were sired by extra-pair males. The frequency of extra-pair offspring within broods was highly skewed with the majority of all broods having either no extra-pair offspring or only extra-pair offspring. Individual pairs were consistent in their frequency of extra-pair paternity among broods, and the repeatability of extra-pair paternity of multiple broods of the same female was statistically significant. The proportion of extra-pair offspring was negatively related to the tail length of the male attending the nest. Behavioural observations showed that extra-pair fertilizations were more likely in broods raised by females that had been observed to engage in extra-pair copulations. The frequency of extra-pair offspring was unrelated to the intensity of two male paternity guards, mate guarding and the rate of intra-pair copulations. In an analysis of extra-pair paternity and male parental care in different broods of the same male, male barn swallows fed their offspring relatively less frequently if the brood contained more extra-pair offspring. Therefore, female barn swallows pursue extra-pair copulations with attractive males, which may result in sexual selection, even though extra-pair paternity is costly for females due to the reduction of paternal care by their social mates. Received: 24 January 1997 / Accepted after revision: 2 August 1997     

Do male tree swallows guard their mates?

Summary We monitored the time spent at the nest and following behavior of mated tree swallows to determine if males were guarding their mates. The proportion of time spent together at the nest did not decrease significantly between fertile and postfertile periods, and the tendency of males to follow females was not significantly different from that of females to follow males. Following by either sex was infrequent. We suggest that the lack of mate guarding in tree swallows is related to an apparently low probability of extra-pair copulations, which in turn is likely to be due to two factors. Nesting opportunities are limited, perhaps more so for females than males. If the operational sex ratio is skewed towards females, this would not only reduce the risk of extra-pair copulations, but would also select against promiscuous females which would risk being abandoned by their mates. Secondly, under natural conditions, the limited availability of nest sites has selected for territorial defense by both males and females, which may decrease the occurrence of extra-pair copulation. Both factors would lead to relaxed selection for mate guarding behavior.     

Different tactics,one goal: initial reproductive investments of males and females in a small Arctic seabird

Despite a great number of studies on extra-pair paternity in birds, the actual roles of males and females in extra-pair contacts is poorly understood, as detailed behavioural studies comparing the reproductive performance of the two sexes prior to egg laying are relatively scarce. Here, we investigated mating behaviour (copulations and aggressive interactions), time budget and body condition (size-adjusted body mass and baseline corticosterone level) in the little auk (Alle alle), a monogamous and highly colonial, Arctic seabird. We performed the study in a large breeding colony of the little auk in Hornsund (Spitsbergen). We found that the males frequently attempted extra-pair copulations (EPCs), although these contacts were almost always unsuccessful, mostly because of the females’ rejection behaviour. These results clearly indicate that genetic monogamy is maintained through female control. Nevertheless, males tried to protect their paternity by staying in close proximity to their females and aggressively intervening when their mates became involved in EPCs. Compared to females, males also spent more time in the colony guarding nest sites. Despite the apparent sex differences in the time budget and frequency of aggressive interactions, body condition was similar in the two sexes, indicating comparable parental investments during the mating period.     

Social and ecological factors affecting paternity allocation in American robins with overlapping broods

Factors that affect extra-pair mating in birds are likely to vary across the breeding season. Changing densities of active nests may alter the opportunities for extra-pair mating, and parental duties may alter a male’s opportunity to guard his mate from extra-pair mating. The latter affects species with multiple broods, where males care for fledglings from first nests while females initiate second nests. We studied a population of multi-brooded American robins (Turdus migratorius) to assess how seasonal changes in nesting density and changes in mate-guarding opportunity influenced paternity patterns over successive breeding attempts. Extra-pair paternity (EPP) occurred in 71.9% of broods and accounted for 48.1% of young. High nesting densities in the study population may explain the high overall rate of EPP, but seasonal variation in breeding density did not explain patterns of EPP among nests. Contrary to the predictions of the mate-guarding hypothesis, EPP did not increase in the second nests that followed successful first nests, and the percentage of extra-pair young in second nests did not decline as the overlap between successive nests increased. The fact that EPP was actually lower when the interval between clutches was shorter suggests that the sooner the males can assume sole care of first broods and allow their mates to renest (indicative of superior paternal quality), the more paternity they realize in the next nest. These results suggest that mate-guarding opportunity does not influence paternity in this population of American robins and that female robins may allocate paternity based on their assessment of male parental performance at first nests.     

Responses of male white ibises to their mate's extra-pair copulations

Summary I intensively observed the mating behavior of 134 pairs of white ibises for over 15 000 pair hours to examine the responses of males to extrapair copulations (EPC) involving their mates. Females often cooperated completely in apparently fertile EPCs. Male mate-guarding was vigorous and effective. Males did not respond to apparent sperm competition with forced-pair copulation, physical punishment, or abandonment of their mates. I found no negative correlation between degree of female promiscuity and the amount of parental care her mate gave to the entire brood. Males also did not reduce paternal care given to the young most likely to be the result of an EPC. I hypothesize that males are constrained in the behaviors they can use to avoid misplaced paternity in this species. While male mate-guarding reduces the opportunities for female involvement in EPC, the behaviors used by males to protect paternity apparently have not prevented the evolution of female receptiveness during EPC attempts.     

Duetting in the subdesert mesite Monias benschi: evidence for acoustic mate defence?

Despite numerous hypotheses proposed for the function of duets, there is currently no consensus as to why males and females should coordinate their songs in such a precise way. There is evidence indicating that duets sometimes serve in territory defence, but additional functions are rarely considered. The mate-defence hypothesis proposes that birds sing in response to their partner's song and the resulting duet repels rivals and may prevent desertion of a partner. We investigated this idea in the subdesert mesite Monias benschi using playback experiments in which we broadcast recordings of solos and duets to single birds and groups. Two predictions of the hypothesis were met: (1) the solo songs of both sexes incited aggressive responses from paired birds of the same sex; and (2) compared to solo songs, pair duets elicited weaker responses from groups and duetting pairs. However, groups responded to male duets with a vigour equal to that with which they responded to male solos. This indicated that the weaker responses of groups to pair duets compared to male solos was a function of the sex rather than number of vocalising birds. Groups responded more strongly to male solos than to either female solos or pair duets, and females' responses were generally weaker than those of males. This may reflect stronger competition among males for mates, due to a male-biased sex ratio in the population. We conclude that song serves similar functions in each sex and that duets may arise through mutual mate defence.     

Crimson-breasted Shrike females with extra pair offspring contributed more to duets

Many socially monogamous bird species follow a genetically promiscuous reproductive strategy. Duetting birds may be an exception, as they appear to exhibit very low levels of extra pair paternity—which is thought to be connected to duetting. Duets are predicted to function either in paternity guarding or as signals of commitment to the pair bond, reciprocally reducing extra pair mating in both sexes. In this study, we used four microsatellites to document paternity loss in the Crimson-breasted Shrike (Laniarius atrococcineus), a socially monogamous subtropical duetting species. Extra pair paternity was surprisingly high, with extra pair males siring 20 % of young in 30 % of broods. Furthermore, we compared the levels of extra pair paternity of each pair to certain characteristics of their duets to test the paternity guard and the commitment hypotheses. Our results offered no support that duets function in paternity guarding, although the fact that males which had been cuckolded answered more of their female’s calls could represent an adaptation to avoid future cuckoldry. We also found no evidence for duets functioning as signal of commitment. Female vocal behaviour was in fact the reverse of that predicted: Levels of infidelity amongst social females were positively related to female answer rate of their mates’ songs. These results indicate that females may use increased answer rates as a form of manipulation, in an attempt to avoid potential costs associated with their extra pair matings.     

Mating opportunities,paternity, and sexual conflict: paternal care in northern and southern temperate house wrens

Males are generally predicted to care less for their young when they have more additional mating opportunities, lower paternity, or when their mates care more. We tested these predictions using male provisioning as a proxy for paternal care in two temperate populations of house wrens (Troglodytes aedon) with divergent life histories. Males in the migratory, occasionally socially polygynous New York, USA (northern) population provisioned less when more local females were fertile. A similar relationship was only weakly supported in the resident, socially monogamous Buenos Aires Province, Argentina (southern) population, possibly due to the higher density of house wrens there. A relationship between male provisioning and level of paternity within the brood was supported in both populations, but in opposite directions: while males in the southern population provisioned less at broods containing more extra-pair young, males in the northern population provisioned such broods more, contradicting predictions. Males provisioned less when their mates provisioned more in both populations, in agreement with sexual conflict theory. Additionally, the populations both exhibited a positive relationship between male provisioning and nestling age, but differed in the direction of the relationships of male provisioning with date and brood size. Our results suggest that even within a species, life history differences may be accompanied by differences in the determinants of behavior such as paternal care.     

Mate guarding,copulation strategies and paternity in the sex-role reversed,socially polyandrous red-necked phalarope<Emphasis Type="Italic"> Phalaropus lobatus</Emphasis>

In a recent review, Westneat and Stewart (2003) compiled evidence that extra-pair paternity results from a three-player interaction in which sexual conflict is a potent force. Sequentially polyandrous species of birds appear to fit this idea well. Earlier breeding males may attempt to use sperm storage by females to obtain paternity in their mates subsequent clutches. Later-breeding males may consequently attempt to avoid sperm competition by preferring to pair with previously unmated females. Females may bias events one way or the other. We examined the applicability of these hypotheses by studying mating behavior and paternity in red-necked phalaropes (Phalaropus lobatus), a sex-role reversed, socially polyandrous shorebird. Male red-necked phalaropes guarded mates more strongly than other shorebirds. Males increased within-pair copulation attempts during their mates fertile period, and maintained or further increased attempts towards the end of laying, suggesting an attempt to fertilize the females next clutch; these attempts were usually thwarted by the female. Paired males sought extra-pair copulations with females about to re-enter the breeding pool. Multilocus DNA fingerprinting showed that 6% of clutches (4/63) each contained one chick sired by a male other than the incubator, producing a population rate of these events of 1.7% (n=226 chicks). Male mates had full paternity in all first clutches (n=25) and 15 of 16 monogamous replacement clutches. In contrast, 3 of 6 clutches of second males contained extra-pair young likely fathered by the females previous mate. Previously mated female phalaropes may employ counter-strategies that prevent later mating males from discriminating against them. The stability of this polyandrous system, in which males provide all parental care, ultimately may depend on females providing males with eggs containing primarily genes of the incubating male, and not a previous mate.Communicated by M. Webster     

Do female black-capped chickadees prefer high-ranking males as extra-pair partners?

Previous studies have shown that some female black-capped chickadees (Poecile atricapillus) solicit copulations from males that rank higher in winter flocks than their social mates, and extra-pair paternity in nests occurs commonly enough to be considered a potential female mating tactic. This study uses blood samples collected in 1992–1995 from 58 families of black-capped chickadees to test whether females with extra-pair offspring have chosen extra-pair sires higher in social rank than their mates. Paternity was assessed with multilocus DNA fingerprinting in 1992–1994 nests and with microsatellite and single-locus minisatellite DNA typing in 1995 nests. Seventeen of 58 nests (29.3%) contained young genetically mismatched with their social father. In 11 of 15 cases where the identity of the extra-pair male was known, the extra-pair male was dominant to the social father. Using data from 29 nests located in 1994 and 1995 for which we had the most data on relative ranks of males, high-ranking males had greater realized reproductive success than low-ranking males as a result of extra-pair fertilizations. There was no significant difference between the number of nests containing extra-pair young of females mated to low-ranked versus high-ranked males. Two nests in 1995 contained young either genetically mismatched with both social parents (intraspecific brood parasitism) or, in one nest, genetically mismatched with the social mother but not the social father (quasi-parasitism). The implications of female strategies acquiring genetic benefits through extra-pair copulations are discussed. Received: 7 July 1997 / Accepted after revision: 14 March 1998