Monogamy in black vultures: genetic evidence from DNA fingerprinting

Recent research has indicated that avian mating systems maycommonly deviate from monogamy due to extrapair fertilizations(EPFs). Because the majority of avian species have long beenconsidered monogamous, accurate measurement of the frequencyof EPFs in a variety of species is important to enhance understandingof the evolution of avian mating systems. We used DNA fingerprintingto investigate the apparently monogamous mating system of blackvultures (Coragyps airaius) by assaying parentage within severalnuclear families. Monogamy is suggested in black vultures becausemated pairs exhibit long-term pair bonding and year-round association,and share incubation and nestling feeding duties equally. Thirtytwobreeders and 36 nestlings representing 16 complete nuclear familieswere tagged for individual identification and sampled for DNAanalysis using 2 restriction enzymes and 3 probes for hypervariableregions. Putative parents were assigned parentage in all cases.We empirically examined the probability of detecting EPFs bycomparing nestlings' fingerprints to those of a putative parentand another randomly chosen adult. All putative parents couldbe assigned with 95%confidence and all outside adults couldbe similarly excluded. There is therefore no evidence for successfulEPFs in this population, indicating a mating system that doesnot deviate from strict monogamy. The complex social behaviorof black vultures may eliminate the opportunity for EPFs dueto the prohibition of copulations in the presence of relatives.     

Evolution of sexual dichromatism in relation to nesting habits in European passerines: a test of Wallace's hypothesis

Wallace proposed in 1868 that natural rather than sexual selection could explain the striking differences in avian plumage dichromatism. Thus, he predicted that nesting habits, through their association with nest predation, could drive changes in sexual dichromatism by enabling females in cavity nesters to become as conspicuous as males, whereas Darwin (1871, The Descent of Man and Selection in Relation to Sex, John Murray, London) argued that sexual selection was the sole explanation for dichromatism. Sexual dichromatism is currently used as indicating the strength of sexual selection, and therefore testing Wallace's claim with modern phylogentically controlled methodologies is of prime interest for comparing the roles of natural and sexual selection in affecting the evolution of avian coloration. Here, we have related information on nest attendance, sexual dichromatism and nesting habits (open and cavity nesting) to male and female plumage conspicuousness in European passerines. Nest incubation attendance does not explain male or female plumage conspicuousness but nest type does. Moreover, although females of monochromatic and cavity nesting species are more conspicuous than females of other species, males of monochromatic and open nesting species are those with more cryptic plumage. Finally, analyses of character evolution suggest that changes in nesting habits influence the probability of changes in both dichromatism and plumage conspicuousness of males but do not significantly affect those in females. These results strongly suggest a role of nesting habits in the evolution of plumage conspicuousness of males, and a role for sexual selection also in females, both factors affecting the evolution of sexual dichromatism. We discuss our findings in relation to the debate that Darwin and Wallace maintained more than one century ago on the importance of natural and sexual selection in driving the evolution of plumage conspicuousness and sexual dichromatism in birds, and conclude that our results partly support the evolutionary scenarios envisaged by both extraordinary scientists.     

RECONSTRUCTING THE EVOLUTION OF SEXUAL DICHROMATISM: CURRENT COLOR DIVERSITY DOES NOT REFLECT PAST RATES OF MALE AND FEMALE CHANGE

Males of sexually dimorphic species often appear more divergent among taxa than do females, so it is often assumed that evolutionary changes have occurred primarily in males. Yet, sexual dimorphisms can result from historical changes in either or both of the sexes, and few previous studies have investigated such patterns using phylogenetic methods. Here, we describe the evolution of male and female plumage colors in the grackles and allies (Icteridae), a songbird clade with a broad range in levels of sexual dichromatism. Using a model of avian perceptual color space, we calculated color distances within and among taxa on a molecular phylogeny. Our results show that female plumage colors have changed more dramatically than male colors in the evolutionary past, yet male colors are significantly more divergent among species today. Historical increases in dichromatism have involved changes in both sexes, whereas decreases in dichromatism have nearly always involved females evolving rapidly to look like males. Dichromatism is also associated with mating system in this group, with monogamous taxa tending to exhibit relatively low levels of sexual dichromatism. Our findings suggest that, despite appearances, female plumage evolution plays a more prominent role in sexual dichromatism than is generally assumed.     

Mating systems among European passerines: a review

A review of the mating systems of 122 relatively well-studied European passerines (out of 172 species) is given. Of all species, 39% are polygynous and 25 of the 47 polygynous species are regular polygynists exceeding the limit of 5% polygyny in a population. Of 46 polygynous species, 63% are monoterritorial (having a maximum of one territory), the rest being polyterritorial (having a maximum of more than one territory). Regular polygyny is more common among polyterritorial passerines. Polygyny is frequently found among species breeding in open habitats (marshes, meadows, pastures and low shrubs). Polyterritorial species tend to have tropical winter quarters more frequently than monoterritorial species do. Colonial breeding is absent from the polyterritorial group. Monogamous male passerines participate more frequently in feeding nestlings than their polygynous counterparts do. Regular polygynists tend to be sexually dimorphic in plumage more often than infrequent polygynous passerines, and polyterritorial passerines similarly tend to be plumage dimorphic more often than monoterritorial species. Sexual size dimorphism was more pronounced in monoterritorial than in polyterritorial passerines.     

Monogamy and long-term pair bonding in vertebrates

The term 'monogamy' represents a complex of mating systems that has been relalively neglected. Monogamy is generally associated with significant biparental care and is most common among birds. Recent work has addressed such aspects as the evolutionary incentives for (and value of) contributions by the male parent, how the distributions of females and critical nesting resources can promote monogamy, male defense of genetic paternity, the causes of long-term mate-retention in certain species, and the subtle means by which sexual selection operates within basically monogamous systems. New advances in testing genetic relatedness, especially DNA fingerprinting, promise much for the assessment of individual costs and benefits of monogamy.     

Monogamy in marine fishes

The formation of long-term pair bonds in marine fish has elicited much empirical study. However, the evolutionary mechanisms involved remain contested and previous theoretical frameworks developed to explain monogamy in birds and mammals are not applicable to many cases of monogamy in marine fish. In this review, we summarise all reported occurrences of social monogamy in marine fish, which has so far been observed in 18 fish families. We test quantitatively the role of ecological and behavioural traits previously suggested to be important for the evolution of monogamy and show that monogamous species occur primarily in the tropics and are associated with coral reef environments in which territory defence and site attachment is facilitated. However, there is little evidence that obligately monogamous species are smaller in body size than species that can adopt a polygynous mating system. We review the evidence pertaining to six hypotheses suggested for the evolution of monogamous pair bonds: (1) biparental care, (2) habitat limitation, (3) low population density/low mate availability/low mobility, (4) increased reproductive efficiency, (5) territory defence, and (6) net benefit of single mate sequestration. We outline predictions and associated empirical tests that can distinguish between these hypotheses, and assess how generally each hypothesis explains monogamy within and between breeding periods for species with different types of territories (i.e. feeding only or feeding and breeding). Hypotheses (1) and (2) have limited applicability to marine fishes, while hypotheses (3)-(5) have little empirical support beyond the species for which they were designed. However, the role of paternal care in promoting monogamous pair bonds is not explicit in these hypotheses, yet paternal care has been reported in more than 70 monogamous marine fish. We show that paternal care may act to increase the likelihood of monogamy in combination with each of the proposed hypotheses through decreased benefits to males from searching for additional mates or increased advantages to females from sequestering a single high-quality mate. Among species defending breeding and feeding territories, the benefits, both within and between reproductive periods, of sequestering a single high-quality mate (hypothesis 6) appear to be the best explanation for socially monogamous pairs. For species without parental care (i.e. holding only feeding territories), territory defence (hypothesis 5) in combination with the benefits of guarding a large mate (hypothesis 6) could potentially explain most instances of monogamy. Empirical studies of marine fishes over the past two decades are therefore slowly changing the view of monogamy from a mating system imposed upon species by environmental constraints to one with direct benefits to both sexes.     

The origins of sexual dimorphism in body size in ungulates

Jarman (1974) proposed a series of relationships between habitat use, food dispersion, and social behavior and hypothesized a series of evolutionary steps leading to sexual dimorphism in body size through sexual selection in African antelope species. The hypothesis states that sexual size dimorphism evolved in a three-step process. Initially, ancestral monomorphic and monogamous ungulate species occupying closed habitats radiated into open grassland habitats. Polygynous mating systems then rapidly evolved in response to the aggregation of males and females, perhaps in relation to the clumped distribution of food resources in open habitats. Subsequently, size dimorphism evolved in those species occupying open habitats, but not in species that remained in closed habitats or retained monogamy. This hypothesis has played an important role in explaining the origins of sexual dimorphism in mammals. However, the temporal sequence of the events that Jarman proposed has never been demonstrated. Here we use a phylogeny of extant ungulate species, along with maximum-likelihood statistical techniques, to provide a test of Jarman's hypothesis.     

Duetting—A mechanism to strengthen pair bonds in a dispersed pair‐living primate (Lepilemur edwardsi)?

Duetting is defined as an interactively organized pair display in which one pair partner coordinates its vocalizations in time with those of the other. It is widespread among tropical birds and cohesive pair‐living primates, in which it is suggested to strengthen pair bonds. We know very little about the presence and function of duetting in dispersed pair‐living mammals. We studied duetting behavior in a solitary foraging, but pair‐sleeping, primate, the Milne Edwards' sportive lemur, in a dry deciduous forest of north‐western Madagascar. We radio‐tracked six pairs throughout 1 year and recorded their sleeping sites and associations, home‐range use, and vocal and behavioral interactions. Three different periods were covered (mating, pregnancy, and offspring care). Sleeping partners form long‐term pair bonds, indicated by an almost exclusive pair‐specific usage of sleeping sites and home‐ranges across periods. We explored three functional hypothesis of duetting: mate reunion, pair reunion, and joint‐territorial defense. Pairs regularly engaged in duet calling. Duetting increased significantly during the offspring care period. Duetting occurred significantly more often at feeding sites than at sleeping sites. Pair partners synchronized behavioral activities after duetting. The activity most often synchronized was locomotion. Pair partners played an equal role in duetting with no difference between sexes in starting or terminating duetting. Altogether, our results provide support for the hypothesis that in dispersed pair‐living primates, duetting evolved as a mechanism to coordinate activities between pair partners dispersed in space, to strengthen pair bonds, and, perhaps, to limit infanticide and nutritional stress in lactating females. Am J Phys Anthropol, 2009. © 2009 Wiley‐Liss, Inc.     

Nest shape explains variation in sexual dichromatism in New World blackbirds

Following Charles Darwin, research on sexual dichromatism has long focused on sexual selection driving ornamentation in males. However, Alfred Russel Wallace proposed another explanation – that dichromatism evolves as a result of selection favoring crypsis in incubating females. Many recent studies suggest that evolutionary changes in sexual dichromatism often result from changes in female, in addition to male, plumage, yet the evolutionary mechanisms driving changes in female plumage remain largely unexplained. To test Wallace's hypothesis, we examined variation in sexual dichromatism and nest shape, a proxy for predation risk, among New World blackbirds (Aves: Icteridae). Phylogenetic models reveal an evolutionary correlation between sexual dichromatism and nest exposure. Specifically, we found that transitions in monochromatic lineages with exposed nests toward either concealed nests or dichromatism were common. Although this evidence supports Wallace's hypothesis that female incubation leads to selection for crypsis or concealment, we also found that transitions to monomorphism were common, even in lineages with exposed nests – a result suggestive of a role for positive selection on female ornamentation. These patterns of plumage evolution support a growing body of work emphasizing the importance of developing and testing hypotheses to explain evolutionary changes in female, as well as male, ornamentation.     

Duet-splitting and the evolution of gibbon songs

Unlike the great apes and most other primates, all species of gibbons are known to produce elaborate, species-specific and sex-specific patterns of vocalisation usually referred to as "songs". In most, but not all, species, mated pairs may characteristically combine their songs in a relatively rigid pattern to produce coordinated duet songs. Previous studies disagree on whether duetting or the absence of duetting represented the primitive condition in gibbons. The present study compares singing behaviour in all gibbon species. Various vocal characteristics were subjected to a phylogenetic analysis using previously published phylogenetic trees of the gibbon radiation as a framework. Variables included the degree of sex-specificity of the vocal repertoire, the occurrence of solo songs, and the preference for a specific time of day for song-production. The results suggest the following scenario for the evolution of gibbon songs: (1) The last common ancestor of recent gibbons produced duet songs. (2) Gibbon duets probably evolved from a song which was common to both sexes and which only later became separated into male-specific and female-specific parts (song-splitting theory). (3) A process tentatively called "duet-splitting" is suggested to have led secondarily from a duetting species to a non-duetting species, in that the contributions of the pair-partners split into temporally segregated solo songs. This appears to be the first time that a non-duetting animal can be shown to be derived from a duetting form. (4) The return to exclusive solo singing may be related to the isolated island distribution of the non-duetting species.     

Pair Swimming and Mutual Partner Guarding in Monogamous Butterflyfish (Pisces,Chaetodontidae): a Joint Advertisement for Territory

The ecology and social systems of Red Sea butterflyfish were studied along the Sinai coast. Distribution, population density and sociography indicate a preponderance of monogamy in all species, independent of reef zonation and seasonal or long-term changes of the reef environment. The social and mating systems are mutual monogamy; partners remain together for up to 6 years. Links between the monogamy and benthic habits of these fish are indicated by their feeding ecology and by a comparison with Indopacific plankton-feeding species, which usually occur in groups. Territories are defended pairwise. Pair partners nearly always remain within visual contact, but a species-typical distance apart. Pair swimming is independent of season or time of day. Experimental partner removals led to speedy replacement of mates. Possible causes of high partner permanency with little partner fidelity are discussed. In good habitats, single territorial adults do not occur. They would be unable to defend and maintain a territory over long periods. While cooperating in defence and maintenance of a territory, each individual can exploit the resources of the territory including availability of a mate. Pair swimming with mutual partner guarding is considered a joint territorial advertisement similar to duetting in birds; it minimizes agonistic interactions between territory holders. As butterflyfish have planktonic larvae without any broodcare, monogamy could not have evolved in response to broodcare activities as in many other vertebrate groups.     

The ecological and evolutionary stability of interspecific territoriality

Interspecific territoriality may play an important role in structuring ecological communities, but the causes of this widespread form of interference competition remain poorly understood. Here, we investigate the phenotypic, ecological and phylogenetic correlates of interspecific territoriality in wood warblers (Parulidae). Interspecifically territorial species have more recent common ancestors and are more similar phenotypically, and are more likely to hybridise, than sympatric, non‐interspecifically territorial species. After phylogenetic corrections, however, similarity in plumage and territorial song are the only significant predictors of interspecific territoriality besides syntopy (fine‐scale geographic overlap). Our results do not support the long‐standing hypothesis that interspecific territoriality occurs only under circumstances in which niche divergence is restricted, which combined with the high incidence of interspecific territoriality in wood warblers (39% of species), suggests that this interspecific interaction is more stable, ecologically and evolutionarily, than commonly assumed.     

Breaking the rules: sex roles and genetic mating system of the pheasant coucal

Generally in birds, the classic sex roles of male competition and female choice result in females providing most offspring care while males face uncertain parentage. In less than 5% of species, however, reversed courtship sex roles lead to predominantly male care and low extra-pair paternity. These role-reversed species usually have reversed sexual size dimorphism and polyandry, confirming that sexual selection acts most strongly on the sex with the smaller parental investment and accordingly higher potential reproductive rate. We used parentage analyses and observations from three field seasons to establish the social and genetic mating system of pheasant coucals, Centropus phasianinus, a tropical nesting cuckoo, where males are much smaller than females and provide most parental care. Pheasant coucals are socially monogamous and in this study males produced about 80% of calls in the dawn chorus, implying greater male sexual competition. Despite the substantial male investments, extra-pair paternity was unusually high for a socially monogamous, duetting species. Using two or more mismatches to determine extra-pair parentage, we found that 11 of 59 young (18.6%) in 10 of 21 broods (47.6%) were not sired by their putative father. Male incubation, starting early in the laying sequence, may give the female opportunity and reason to seek these extra-pair copulations. Monogamy, rather than the polyandry and sex-role reversal typical of its congener, C. grillii, may be the result of the large territory size, which could prevent females from monopolising multiple males. The pheasant coucal’s exceptional combination of classic sex-roles and male-biased care for extra-pair young is hard to reconcile with current sexual selection theory, but may represent an intermediate stage in the evolution of polyandry or an evolutionary remnant of polyandry.     

The role of sexual and natural selection in shaping patterns of sexual dichromatism in the largest family of songbirds (Aves: Thraupidae)

Males and females can be under different evolutionary pressures if sexual and natural selection is differentially operating in each sex. As a result, many species have evolved sexual dichromatism, or differences in coloration between sexes. Although sexual dichromatism is often used as an index of the magnitude of sexual selection, sexual dichromatism is a composite trait. Here, we examine the evolution of sexual dichromatism in one of the largest and most ecologically diverse families of birds, the tanagers, using the avian visual perspective and a species‐level phylogeny. Our results demonstrate that the evolutionary decreases of sexual dichromatism are more often associated with larger and more frequent changes in male plumage coloration, and evolutionary increases are not more often associated with larger changes in either sex. Furthermore, we show that the crown and ventral plumage regions are correlated with sexual dichromatism in males, and that only male plumage complexity is positively correlated with sexual dichromatism. Finally, we demonstrate that light environment is important in shaping both plumage brilliance and complexity. By conducting a multilevel analysis of plumage evolution in males and females, we show that sexual dichromatism evolves via a mosaic of sexual and natural selection in both sexes.     

Is the juvenal plumage of altricial songbirds an honest signal of age? Evidence from a comparative study of thrushes (Passeriformes: Turdidae)

The function and evolution of avian plumage colouration has been the subject of many studies over the past decade, but virtually all of this research has focused on the plumages of sexually mature individuals. The colours and patterns of juvenal plumage, which is worn by altricial songbirds only for the first few months of life, have been the focus of few studies. We develop the idea that distinctive juvenile appearance may be a signal of sexual immaturity, serving to reduce aggression from conspecific adults. We use a comparative phylogenetic approach to test this hypothesis in the thrushes (Family Turdidae). Honest signals of reproductive immaturity should be more valuable when juveniles fledge into environments with aggressive adult conspecifics. Therefore, we predicted that distinctive juvenile appearance would be more likely to evolve in species with extended breeding seasons and high levels of territoriality. Because many tropical bird species exhibit year‐round territoriality and elongated breeding seasons, we used breeding latitude as a proxy for these variables. As predicted, distinctive juvenile appearance was significantly correlated with occupancy of tropical latitudes. While alternative explanations cannot be ruled out and more tests of the hypothesis are needed, the observed associations between breeding latitude and distinctiveness of juvenal plumage are consistent with our hypothesis that distinctive juvenal plumage evolved as a signal of sexual immaturity.     

High rates of infidelity in the Grey Fantail Rhipidura albiscapa suggest that testis size may be a better correlate of extra‐pair paternity than sexual dimorphism

The Grey Fantail Rhipidura albiscapa is a socially monogamous passerine endemic to Australia. Behavioural and morphological clues point to opposing conclusions as to its breeding system; sexual monomorphism and monochrome colorations suggest monogamy, whereas relatively large testes and a prominent cloacal protruberance are more indicative of multiple mating and sperm competition. We used five highly variable microsatellite loci to investigate the genetic breeding system of this species. Paternity was assigned to 49 of 69 (71%) offspring tested and the overall rate of partner infidelity was high, with 55% of offspring being sired by an extra‐pair male and 64% of all clutches containing extra‐pair young. This puts the Grey Fantail amongst the most promiscuous socially monogamous species yet studied. Where extra‐pair fathers were identified, these were invariably in neighbouring territories, and although larger males did not gain more paternities overall, extra‐pair offspring tended to be fathered by larger males than expected by chance. We interpret our findings in light of some of the potential costs and benefits associated with extra‐pair paternity.     

Engines of speciation: a comparative study in birds of prey

Sexual selection as a promoter of speciation has received much attention in recent years, but has produced highly equivocal evidence. Here, I test whether sexual conflict is related to species richness among genera in accipitrid birds of prey using phylogenetically controlled comparative analyses. Increased species richness was associated with both 'male-win' as well as 'female-win' situations, i.e. males being able to promote gene flow through mating or females being able to restrict gene flow through female choice. Species richness was higher when plumage differed between males and females and in polygynous breeding systems compared with monogamous ones. To assess the relative importance of sexual conflict and natural selection as correlates of species richness simultaneously, I also performed a multivariate analysis of correlates of species richness. Population density, plumage polymorphism, geographic range size and breeding latitude were predictors of species richness for birds of prey. These results stress the importance of both sexual and natural selection in determining species richness but with a clear overall emphasis on natural selection in birds of prey.     

TEMPORAL PATTERNS OF DUETTING IN AFRICAN BARBETS

Four species of African barbets ( Lybius torquatus, L. vieilloti, Trachyphonus darnaudii , and T. erythrocephalus ) regularly sing in duet. Duets consist of phrases repeated at very regular intervals; in L. torquatus and L. vieilloti the standard deviation is less than a tenth of the mean interval between duet motifs. Sound spectrographic analysis of the songs indicates that an internal rhythmic behaviour pattern determines in large part the temporal features of the duet in these barbets:(1) one member of a pair of L. torquatus continues to call in rhythm even though its mate may call irregularly, (2) in the other three species the calling rhythm of each of the two mates is different, especially in L. vieilloti where the ratio of the periodicity of calling of the two birds averages 1:1^.52 and where one bird continues to call at the same rate when its mate ceases to call, and (3) several non-duetting African barbets have regular calling periodicities, some with greater precision than in the duetting barbets and some with less. In the barbets the temporal pattern of duets appears to be in greater degree determined by individual calling rhythms (as in some non-duetting barbets) than by the auditory reaction time involved in a bird responding to its mate. Duetting in barbets probably functions both in maintenance of a pair bond and in territorial advertisement.     

Low frequency of extrapair paternity in the common redstart ( Phoenicurus phoenicurus )

Social monogamy is common among passerines whereas genetic monogamy is regarded as rare. Here we report the first study of paternity in the genus Phoenicurus (Aves, Muscicapidae). In the socially monogamous common redstart (Phoenicurus phoenicurus) 2.0% (5/253) of offspring in 10.5% (4/38) of the broods examined were sired by extrapair males. The observed pattern of extrapair paternity was consistent among two geographically separate nest-box populations sampled over two years. Our findings reveal low rates of extrapair paternity compared with other passerine birds, suggesting only a minor role of sperm competition in this sexually dichromatic species.     

Are Monomorphic Species Really Sexually Indistinguishable: No Evidence in Wild Long‐Tailed Finches (Poephila acuticauda)

Studies of sexual selection have focused mainly on dimorphic and/or polygynous species, where males, typically possess more exaggerated secondary sexual characters. However in many species, receiving far less attention, the expression of ornamental traits by females matches that in males. Several hypotheses have been proposed to explain sexual monomorphism, including mutual mate choice, genetic correlation, weak sexual selection and sexual indistinguishability. The sexual indistinguishability hypothesis suggests that sexual monomorphism is an adaption to avoid competition in monogamous flock‐living species. Based on measurements of museum skins and domesticated birds in Europe, the Australian long‐tailed finch was classified as a sexually monomorphic species, providing the best empirical support for the sexual indistinguishability hypothesis. Using both domestic and wild long‐tailed finches, we have re‐evaluated the extent to which the sexes are really indistinguishable. Morphological measurements of wing, tail, tail streamers, tarsus, bill and patch size, and colour spectrometric measurements of the yellow upper mandible and grey crown, were compared between the sexes. While the sexes are similar, males and females nonetheless differed in seven of ten traits in wild populations. In domestic populations, the sexes differed to a lesser extent but were still significantly different at three of ten traits, and discriminant analysis showed that 92% of wild individuals and 89% of domestic individuals could reliably be sexed based on just these morphological traits. Contrary to previous work, this study demonstrates that wild long‐tailed finches are sexually dimorphic, and that the similarity between males and females in this species cannot be explained by the sexual indistinguishability hypothesis.