Extrapair paternity in hooded warblers

We examined the role of extrapair fertilizations (EPFs) in themating system of the hooded warbler (Wilsonia citrina), a monogamoussongbird. DNA fingerprinting revealed that 8 of 17 (47%) femaleshad extrapair young in their first or second brood, and 23 of78 (29%) nestlings were the result of EPFs. Extrapair youngwere signifkandy more likely to occur in first broods than insecond broods. The proportion of EPFs within a brood was stronglybirnodal among broods: nests had 50% or more extrapair youngor none. In seven of eight broods where EPFs occurred, an adjacentmale neighbor was identified as the actual father. Male-likecoloration in females did not reduce the likelihood of havingextrapair young. Females with extrapair young did not receiveless parental care from their mates. All males who obtainedEPFs were mated to fertile females or were feeding offspringat the time they most likely mated with the extrapair female.Our results are consistent with the female control hypothesis,which predicts that females benefit from extrapair copulations(EPCs) and have some control over which males, if any, obtainEPCs. However, we could not reject the alternative hypothesisthat some male neighbors are particularly dominant and aggressiveduring EPC attempts, so females accept these EPCs to minimizecosts.     

Effects of breeding density, synchrony, and experience on extrapair paternity in tree swallows

Breeding density, synchrony, and experience are expected toinfluence the frequency of extrapair paternity in birds. UsingDNA fingerprinting, we examined the effect of these factorson tree swallows nesting at relatively high (grids of nest-boxes)and low (solitary boxes at least 100 m from the nearest neighbor)densities and in relatively synchronous (Alberta) and asynchronous(Ontario) populations in Canada. The mean percentage of extrapairoffspring per nest did not differ significantly between birdsnesting in grids (43%, n = 22 families) and solitary boxes (57%,n = 12 families). Similarly, there was no significant differencein the mean percentage of extrapair offspring per nest betweenrelatively synchronous (60%, n = 12 Alberta families) and asynchronous(41%, n = 22 Ontario families) populations. We also found noconsistent pattern between extrapair paternity and breedingexperience among seven males and seven females examined overtwo to three breeding seasons. Female tree swallows can influencethe fertilization success of extrapair males by active selectionand rejection of copulation partners. We suggest that this abilitylimits the predicted effect of various ecological factors onthe frequency of extrapair paternity     

Genetic monogamy in the absence of paternity guards: the Capricorn silvereye, Zosterops lateralis chlorocephalus, on Heron Island

We investigated the genetic mating system of a socially monogamous passerine bird, the Capricorn silvereye Zosterops lateralis chlorocephalus, on an island of the Great Barrier Reef. Therewere no cases of extrapair paternity (EPP) among 122 offspringfrom 53 broods detectable by minisatellite or microsatelliteDNA fingerprinting. Behavioral observations of paired birdsshowed that this was not a consequence of efficacious paternityguards and that females did not engage in extrapair copulation(EPC). Frequency of intrapair copulations was also low, withonly 14 cases observed during 199 hours of observations ofthe 11 focal pairs in the fertile periods of females, and thiswas consistent with anatomical features of the cloacal protuberancein males. In this population, young birds form life-time pairbonds soon after gaining independence but females are obviouslynot attempting EPC possibly to redress this early mate choice.This is despite the fact that they breed in high density witha synchronous start and asynchronous spread of laying in aprotracted season and males do not positively exhibit mateguarding behavior when females are fertile. Our results supporthigh fidelity of socially monogamous birds on islands and are consistent with the hypothesis that sexual selection is reducedwhere genetic variation in fitness is limited.     

Patterns and correlates of extrapair paternity in American redstarts (Setophaga ruticilla)

We examined correlates and hypotheses pertaining to extrapairfertilizations in socially monogamous American redstarts (Setophagaruticilla). DNA fingerprinting revealed extrapair fertilizationin 59% of broods (19 of 32), involving 40% of nestlings (43of 108). Fewer broods than expected had mixed paternity, asdetermined from a binomial distribution of extrapair young inthe population. This result is consistent with the "good genes"hypothesis, but not with the "genetic diversity" hypothesis.There was a negative association between the age of putativefathers and the proportion of extrapair young in their broods.Irrespective of age, males with prior residency were cuckoldedless often than males new to the study area. Extrapair fatherswere' immediate neighbors in 7 of 10 cuckolded broods whereall neighbors were sampled. Males were more likely to sire offspringin the territories of younger neighbors than in those of olderneighbors. Plumage characteristics of adult males, breedingsynchrony of females, and breeding densities were not significantlyassociated with cuckoldry. Realized reproductive gain from cuckoldrywas small because of high nest predation in our area. Extrapairfertilizations allowed one-quarter of males whose own nestshad failed to achieve some reproductive success. Only 2 of 17males whose own nests were successful also had extrapair young.There was no egg dumping by females. We conclude that male ageand prior residency were predictors of cuckoldry in Americanredstarts. In the context of the heavy predation experiencedby our birds, extrapair fertilizations allowed many males tosalvage some reproductive success and did not increase the varianceof success across males     

Low frequency of extrapair paternity in the polygynous great reed warbler, Acrocephalus arundinaceus

We carried out DNA fingerprinting on 553 young (130 broods)great reed warblers (Acrocephalus arundnaceus) in 1987–1991.In the study population, where 40% of the males become polygynous,there was a low frequency of extrapair fertilizations (EPF).When data from all five years were pooled, 3.1% of the youngwere sired by extrapair males (EPF-males) and 5.4% of the broodscontained extrapair young. We found no cases of extrapair maternity;young with 6–17 mismatched DNA bands (n= 17) had highband sharing with their putative mothers (range = 0.52–0.72)but low band sharing with their putative fathers (range = 0.24–0.40).In broods exposed to EPF, on average 53% of the young were siredby EPF-males. We found the genetic father to each of the illegitimateyoung. In all cases the same EPF-male sired all extrapair youngin a brood. Broods containing EPF-young tended to be initiatedlate during the breeding season. Breeding attempts were ratherevenly distributed over two months, thus this breeding asynchronywould have facilitated EPFs. There was no difference in EPFfrequency between broods where the pair males had left theirfemales unguarded during parts of their fertile periods andbroods where males guarded throughout the fertile periods. Nestswith extrapair young had significantly shorter mean distanceto the closest male neighbor and more male neighbors within100 m than nests without extrapair young. We found no indicationthat females engaged in EPF to get parental care from the EPF-males,or because they were forced to copulate with extrapair males.The low frequency of EPF suggested that females did not seekgenetic diversity to their brood. We cannot rule out the possibilitythat females engaged in EPF to insure fertility. However, datasupporting this hypothesis were weak. Instead, our data supportthe conclusion that females engaged in EPF to increase the geneticquality of their offspring, and that females may have used malesong repertoire size as a cue when choosing EPF partners.     

Ecological determinants of extrapair fertilizations and egg dumping in Alpine water pipits (Anthus spinoletta)

Behavioral ecology has successfully explained the diversityin social mating systems through differences in environmentalconditions, but diversity in genetic mating systems is poorlyunderstood. The difference is important in situations whereparents care for extrapair young (EPY) originating from extrapairpaternity (EPP), extrapair maternity (EPM), and intraspecificbrood parasitism (IBP). In birds, IBP and EPM are rare, butEPP is widespread and highly variable among species and populations.Explanations for this variability are controversial, mainlybecause detailed ecological information is usually lacking inpaternity studies. Here we present results of the first studyto identify the ecological determinants of extrapair activitiesfor both sexes of the same species, the water pipit (Anthusspinoletta). DNA fingerprints of 1052 young from 258 nests revealedEPP in 5.2% of the young from 12.4% of the nests. EPM and IBP,both involving egg dumping (EDP), each occurred in 0.5% of theyoung from 1.9% of the nests. Nests with and without EPY couldnot be distinguished by traits of the breeders and by reproductivesucccess, but they differed with respect to ecology: nests withEPP young were characterized by asynchronous clutch initiation,nests with EPM and IBP young were characterized by higher overlapwith neighboring territories and closer proximity to communalfeeding sites. We suggest that chance events, resulting fromthe temporal and spatial distribution of broods, offer a betterexplanation for the occurence of extrapair activities than femalesearch for genetic or phenotypic benefits. This possibilityof "accidental" extrapair reproduction as an "ecological epiphenomenon"with low potential for selection should also be considered forspecies other than the water pipit.     

Polygyny and extrapair fertilizations in eastern red-winged blackbirds (Agelaius phoeniceus)

Parentage of nestling red-winged blackbirds (Agelaius phoeniceus)from an eastern population was determinedusing DNA fingerprintingtechniques. Of 235 nestlings surveyed, 58 had fingerprints excludingthemale, but none excluded the female tending the nest. Data onpairing status during the female's fertilizable period was availablefor 232 offspring; 55 (25%of 1988 nestlings, 23% of 1989 nestlings)of those were sired through extrapair copulations. Of these55 offspring, 33 could be assigned to nearby territory holders;16 of the remaining nestlings may have been sired by nearbymales that were not captured. During both years, 44% of territorialmales had more than one female nesting simultaneously on theirterritory. The number of extrapair fertilizations gained bymales increased significandy with harem size in 1 year. Paternity(die proportion of nesdings on the territory sired by die territoryholder) showed a positive but nonsignificant increase widi haremsize in bodi years. There was no apparent cost in paternityfor males guarding two or more fertilizable females at the sametime. The broods of females that were fertilizable at die sametime anodier female was setding on die same territory tendedto have a greater proportion of extrapair fertilizations (0.37)than did die broods of odier females within harems (0.15). Establishedfertilizable females were chased significantly more by die territoryowner and by extrapair males when a new female was setding.There were no associations between a male's paternity or successat gaining extrapair fertilizations and his age or color-bandcombination. Overall, extrapair fertilizations had litde effecton die relationship between fledgling success and harem sizeand appeared to have a minimal impact on die overall intensityof sexual selection on males.     

Extrapair paternity in the great tit (Parus major): a test of the "good genes" hypothesis

In 1993 and 1994 we determined the frequency of extrapair paternityin broods of great tits, Parus major using multilocus DNA fingerprinting.We found no instances of intraspecific brood parasitism, but40% of broods (31/78) contained extrapair-fathered young and83% of offspring (58/681) were xtrapair We identified the geneticfathers of 60% of the extrapair nestlings (35/ 58). Males withfull and lost paternity did not differ significantly in traitsthat have been suggested to indicate male quality, nor did thegenetic and social fathers of extrapair offspring. In 1993,cuckolded males sired more offspring that recruited to the subsequentbreeding season than males with full paternity. Moreover, eventhough genetic fathers of extrapair young (EPY) sired more fledglingsthan the males they cuckolded, genetic and social fathers ofEPY did not differ in the number of recruits sired. Also, theEPY of a brood did not survive better than their half sibs.Thus, our results do not supportthe hypothesis that femaleschoose better quality males for extrapair matings ("good genes"hypothesis). Further, the level of extrapair paternity differedmarkedly between the two years. Our data show that females areconstrained in their extrapair activities by the availabilityof extrapair mates. This is at least partly due to yearly differencesin breeding synchrony.