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.     

Territorial intrusions and copulation patterns in red kites, Milvus milvus, in relation to breeding density

Two main paternity assurance strategies are generally found in birds: mate guarding and frequent copulations. The latter is expected particularly in species such as raptors that cannot guard their mates efficiently because of ecological constraints, such as frequent courtship feeding. I investigated the prelaying behaviour of red kites, in which the males courtship feed. I compared pair behaviour in situations of varying breeding density and simulated male territorial intrusions by presenting decoys. Males' certainty of paternity was likely to decrease with increasing breeding density, because of the proximity of other males and more frequent male territorial intrusions during the presumed fertile period. The percentage of time spent by males within their breeding territory during the prelaying period was positively related to the number of close breeding neighbours, suggesting territory surveillance and mate guarding. The kites copulated frequently and over a long period. Copulation frequency prior to and during laying increased with breeding density, and in isolated pairs in response to simulated male territorial intrusions. The results support the idea of paternity assurance through frequent copulations during the presumed fertile period of the female, and suggest that early copulation activity is related to functions other than fertilization, such as pair bonding or mate assessment. Copyright 2000 The Association for the Study of Animal Behaviour.     

Breeding synchrony and extrapair paternity in a species with alternative reproductive strategies

Breeding synchrony may affect the tradeoff between pursuing multiple mates and avoiding paternity loss, translating into differences in the rate of extrapair paternity (EPP). However, diverse empirical relationships between breeding synchrony and EPP remain challenging to explain. We examined whether the relationship between breeding synchrony and EPP varied with male morph, age, body size, or breeding density in the white‐throated sparrow Zonotrichia albicollis. In this species, males of two genetically determined morphs pursue alternative mating strategies. Breeding synchrony positively correlated with EPP within polygamous white morph males, which have high rates of EPP and cuckoldry, but was unrelated to EPP within tan morph males, which prioritize mate guarding and paternal care. As previously reported, males that gained EPP were primarily white males. Males gained EPP more often than expected by chance during their mate's fertile period and on neighboring territories. Since extrapair copulation appears primarily male‐driven in this species, these results indicate that white males focus extra‐pair mating effort during periods of high synchrony and during their mates’ fertile periods, even at the expense of paternity loss within their own nests. Breeding density, male age, and male size did not modify the relationship between breeding synchrony and EPP. However, older white males had higher cuckoldry rates, perhaps reflecting declines in performance associated with senescence. Results suggest that, even within species, mating strategy may modify how breeding synchrony affects rates of EPP, with positive relationships manifest only within subsets of individuals that pursue a strategy of polygyny at the expense of paternity loss.     

Male share of provisioning is not influenced by actual or apparent loss of paternity in western bluebirds

Approximately 45% of western bluebird (Sialia mexicana) femaleshave some chicks in the nest that are not sired by their socialmates. Extrapair fertilizations account for 42% of offspringin these nests and 19% of nestlings overall. I tested the hypothesisthat males reduce nestling provisioning when their certaintyof paternity or share of paternity is reduced. Capture and detentionof socially monogamous males for 1 h or 24 h during the layingperiod reduced males' copulatory access and their ability tomate guard, increasing the frequency with which extrapair malesintruded and attempted to copulate with resident females. Malesdetained during laying did not reduce their share of feedingtrips compared to control males detained during incubation,compared to unmanipulated males, or compared to males that werecaptured but not detained. Males detained on territory for 1h during the laying period did not reduce their share of feedingtrips when they observed male intrusion, nor when they observedtheir mates accepting extrapair copulations. Males that witnessedtheir mates accepting extrapair copulations did not reduce theirshare of risk in provisioning. Genetic fingerprinting at nonexperimentalnests indicated that males also failed to reduce their feedingcontributions when their estimated share of paternity was reduced,even when a helper male was present to reduce the impact onnestlings. These results suggest that male western bluebirdsdo not make significant adjustments in their share of provisioningwhen they have evidence of partial paternity loss. Togetherwith prior results, this study suggests that western bluebirdmales use an all-or-none rule, contributing approximately halfof the parental provisioning at nests, as long they have somecopulatory access to the female during egg laying.     

Male shrikes punish unfaithful females

The costs to females of participating in extrapair copulationsis an interesting but hitherto neglected topic in behavioralecology. An obvious potential cost to females is male physicalsanctions. However, although retaliation and punishment by malepartners has been proposed as a basic cost for female extrapairbehavior in theory, it has not been experimentally demonstrated.We studied the breeding biology of the lesser gray shrike (Laniusminor) and combined field observations and a field experimentto show that (1) there is a high intrusion rate during the female'sfertile period, and extrapair copulations occur in this population;(2) by detaining females during the fertile phase, males wereinduced to retaliate physically against their partners, therebyincreasing costs related to female extrapair behavior; and (3)there were no obvious costs to males of punishing their mates.DNA fingerprinting reveals that extrapair paternity is rareor absent in this population. Although we cannot conclude thatmonogamy at the genetic level is the result of male retaliation,we do show that male physical sanction is a cost that deceptivefemales have to assume. Males' strategies based on coercionshould be considered when explaining variation in extrapairpaternity across species.     

Part-Time Mate Guarding Affects Paternity in Male Reed Buntings (Emberiza schoeniclus)

Male mate guarding by close following has been reported in many socially monogamous bird species and is generally believed to function as a paternity guard. Many aspects of the dynamics and effectiveness of this behavior are still however poorly understood. Here, we describe the temporal variation in mate guarding behavior in male reed buntings (Emberiza schoeniclus) with a particular focus on how males allocate their mating effort between mate guarding and extrapair mating in a context of intense sperm competition. In our highly synchronous study population most males have to balance the simultaneous and mutually exclusive demands of mate guarding and seeking extrapair copulations (EPCs). We found that males frequently switched between guarding their mates and performing intrusions to neighboring territories. Both activities seemed to have significant fitness payoffs, as male mate guarding effort had a positive effect on paternity, and a large fraction of extrapair fertilizations occurred during the days when the sire guarded its own female. The reed bunting is thus an example of how discontinuous or part‐time mate guarding can still be effective in securing paternity. Female reed buntings were not particularly active in initiating EPCs as they never were observed performing extraterritorial forays. We argue that the absence of female‐initiated EPCs is a prerequisite for males to trade mate guarding against seeking EPCs. Otherwise, if females circumvent male mate guarding by timing their EPCs to periods of male absence, males should guard their mates almost continuously or rely on alternative paternity guards.     

Sperm Competition and Copulation Intervals of the White Spoonbill (Platalea leucorodia,Aves, Threskiornithidae)

Some aspects of sperm competition were studied in the white spoonbill (Platalea leucorodia) breeding in Doñana National Park (SW Spain). Shorter pair copulation intervals occurred during the prelaying period, when females were subjected to a relatively high frequency of extra-pair copulations. Pair copulation intervals with an intermediate extra-pair copulation by the male mate were longer than those without extra-pair copulation. This result indicates that males need a time of recovery between copulations before they can perform another. Extra-pair copulations by the females did not affect the length of intervals between pair copulations. There were no differences between the lengths of the intervals between an extra-pair copulation by the female and the following pair copulation for cases in which the male mate detected an intruder male attempting copulation with his mate and those in which the intruder remained undetected. However, the correlations obtained between copulatory intervals for detected and undetected cases suggest a copulatory response by their mates, although affected by the required recovery time between copulations by the males. Finally, since extra-pair copulations mainly occurred while male mates were collecting nest material, they engaged in this activity shortly after pair copulations, probably to avoid a last-male advantage under the sperm competition pressure.     

Decoy presentations as a means to manipulate the risk of extrapair copulation: an experimental study in a semicolonial raptor, the Montagu's harrier (Circus pygargus)

Mate guarding and frequent copulations are two alternative paternity assurance strategies found in birds. In species with intensecourtship feeding, like raptors, the "frequent copulation"strategy is expected because male food provisioning conflictswith mate guarding. We evaluated experimentally the paternityassurance behavior of a semicolonial raptor, the Montagu'sharrier Circus pygargus, using decoy presentations to simulateterritorial intrusions. Breeding pairs were exposed to maleand female decoys at different periods during the female's reproductive cycle. Agonistic responses to decoys were intra-sexual,and the timing and intensity of male attacks toward male decoyssupported responses related to the risk of extrapair copulation(EPC): Male aggression peaked during the presumed fertile periodand almost disappeared after clutch completion. During thefertile period, copulation rate was significantly higher, andcopulations lasted longer, during male decoy presentations than during controls. Males also spent more time close to the femaleduring male decoy presentations compared to controls, bothduring the early prelaying and fertile periods, but not duringincubation. In the fertile period, males also increased presencetime close to the female in the hour following the removal of the male decoy. Conversely, female decoy presentations hadno significant effect on copulatory behavior or male presencetime. These results showed that the risk of EPC can be experimentallymanipulated by the means of decoy presentations, simulatingmale territorial intrusions, and that male Montagu's harriersincrease their short-term copulation frequency and female surveillancewhen they perceive themselves at an increased EPC risk.     

Fitness consequences of helping behavior in the western bluebird

We examined the fitness consequences of helping behavior inthe western bluebird (Sialia mexicana) at Hastings Reservationin Carmel Valley, California, USA, and tested hypotheses forhow helpers benefit from engaging in alloparental behavior.Both juvenile and adult western bluebirds occasionally helpat the nest During a 12 year period, all adult helpers and mostjuvenile helpers were male. Helpers usually fed at nests ofboth their parents and rarely helped when only one parent waspresent. The frequency of pairs with adult helpers was only7%, but nearly one-third of adult males helped among those withboth parents on the study area. At least 28% were breeders whosenests failed. The propensity to help appears to depend uponparental survival, male philopatry, and the breeding successof potential helpers. Feeding rates were not increased at nestswith juvenile helpers, apparendy because breeding males reducedtheir feeding rates. In contrast, adult helpers increased theoverall rates of food delivery to the nest in spite of a reductionin the number of feeding trips made by both male and femaleparents. Helpers did not derive any obvious direct fitness benefitsfrom helping, but they had greater indirect fitness than nonhelpersdue to increases in nestling growth rates and fledging successat their parents' nests. Helpers fledged fewer offspring intheir first nests than did nonhelpers, suggesting that theywere birds with reduced reproductive potential. Although wehave not yet measured the effect of extrapair fertilizationson the fitness benefits of helping, we calculated the differencein fitness between helpers and nonhelpers as a function of thepotential helper's paternity when breeding independently andhis father's paternity in the nest at which he might help. Inconjunction with constraints on breeding and indirect fitnessbenefits, we predict that relatedness of males to the youngin their own as well as their parents' nests will influencehelping behavior in western bluebirds.     

Female begging in European robins: do neighbors eavesdrop for extrapair copulations?

Female European robins beg for food from their mates throughoutthe breeding season using far-carrying "seep" calls which resemblethe begging calls of fledglings. We investigated the possibilitythat these calls are eavesdropped by neighboring males andused as cues to target intrusions during the fertile period.Female seep calling and male courtship feeding peaked in thefertile period, and males appeared to modify provisioning rate in relation to seep calling rate. Further, there was a positivecorrelation between rate of courtship feeding and clutch size,both of which tended to be inversely related to seep callingrates. These observations imply that the seep call is a hungersignal directed at pair males. As the signal is loud and givenmost frequently during the fertile period, it must also contain information about fertility and location. Playback experimentssuggested that this information is eavesdropped by neighboringmales, who responded to rapid rates of seep calling more readilythan slow rates and to calls broadcast at the edge of territoriesrather than their center, presumably in search of extrapaircopulations. Pair males can reduce the intensity of the female's signal by courtship feeding, and thus male provisioning mayprotect paternity.     

Symmetrical male sexual ornaments, paternal care, and offspring quality

Simultaneous manipulation of tail length and tail asymmetryin male barn swallows (Hirundo rustica) has revealed that femalesprefer maJes with both long and symmetrical tail ornaments overmales with short and asymmetrical ornaments. Fluctuating asymmetryin tail length has a negative effect on the maneuvering abilityof male barn swallows, and females may prefer males with symmetricaltail ornaments because they thereby acquire more direct fitnessbenefits in terms of paternal care. The least preferred maleswith short tails with high asymmetry performed an absolutelyand relatively larger share of feeding of nestlings than themost preferred males. However, the combined feeding rate ofthe pair was not statistically significantly different betweentreatment groups. Fully grown tarsus length and body mass ofoffspring on day 15 did not differ between treatments. Theseresults indicate that females do not prefer males with symmetricaltail ornaments because such males contribute a relatively orabsolutely larger share of parental duties. Although these resultsdo not explain the basis of female choice for long and symmetricaltails, the results are consistent with a hypothesis that femalesof species with biparental care should invest differentiallyin their offspring relative to the quality of their mates. Theresults are also consistent with a hypothesis that preferredmales have access to mates with superior parenting abilities     

Kin Recognition and Incest Avoidance in Toads

Toads, like many amphibians, display breeding site fidelity.Individuals that return to natal ponds to breed are likely toencounter siblings as potential mates. We examined the geneticstructure of Bufo americanus breeding populations at five localitieswithin a 1 km radius. Mitochondrial DNA (mtDNA) haplotypes significantlydiffered among the breeding populations, but haplotype distributionsdid not differ from year to year within breeding sites. Natalphilopatry may account for these results. Although incest isthus possible, siblings rarely mate. Comparing haplotypes oftoads captured while mating, we found only 2 of 86 pairs thatcould possibly be siblings. We suggest that toads might recognizeand actively avoid close kin as mates. Advertisement vocalizationsgiven by males serve as potential cues by which females mightrecognize their kin. We recorded calls of males, in the field,and later obtained rank estimates of their relationships toone another by DNA fingerprinting of the nuclear genome. Theresemblance of males' calls was positively correlated with thesimilarity of their fingerprints. Significant differences incall characteristics were also found among breeding populations.Temporal parameters, rather than frequency components, encodekinship information. Recently developed techniques in moleculargenetics facilitate studies of the heritability of behavioraltraits in natural populations.     

Facultative response to a kleptoparasite by the cooperatively breeding pied babbler

In many cases of interspecific kleptoparasitism, hosts developdefensive behaviors to minimize the impact of kleptoparasites.Because vigilance and defensive behaviors are often costly,selection should favor hosts that adjust the amount of investmentneeded to minimize losses to kleptoparasitism. However, examplesof such facultative responses are rare. Here, we investigatethe response of cooperatively breeding pied babblers (Turdoidesbicolor) to the drongo (Dicrurus adsimilis), an avian kleptoparasitethat regularly follows pied babbler groups, often giving alarmcalls to alert the group to predators but also occasionallygiving false alarm calls in order to steal food items. We showthat pied babbler response to drongos varies markedly accordingto babbler group size. In small groups, where there are fewindividuals available to act as sentinels, babblers sentinelless when a drongo is present and respond strongly to drongoalarm calls. However, in large groups, where there are manyindividuals available to participate in predator vigilance,babblers sentinel more often when a drongo is present, rarelyrespond to drongo alarm calls, and aggressively displace drongos,with a consequent decline in the number of successful kleptoparasitismevents. This behavior represent a facultative response to akleptoparasite according to the costs versus benefits of toleratingtheir presence.     

Costs and benefits of variable breeding plumage in the red-backed fairy-wren

The red-backed fairy-wren is a socially monogamous passerine bird which exhibits two distinct types of breeding male, bright males that breed in bright red and black plumage and dull males that breed in dull brown plumage. Most males spend their first potential breeding season in dull plumage and subsequent breeding seasons in bright plumage, but a relatively small proportion of males develop bright plumage in their first breeding season. This study quantifies morphology, behavior, and reproductive success of dull and bright males to assess the adaptive costs and benefits of bright plumage while controlling for age. Older bright males (two years of age or older) attempted to increase their reproductive success via copulations with extrapair females, whereas younger (one-year old) bright males and dull males did not. Thus, older bright males spent less time on their own territories, intruded on neighboring groups with fertile females more frequently, gave more courtship displays, and had larger sperm storage organs than did younger bright males and dull males. Microsatellite analyses of paternity indicate that the red-backed fairy-wren has extremely high levels of sexual promiscuity, and that older bright males had higher within-brood paternity than dull males or younger bright males. Regardless of age, bright males were more attractive to females in controlled mate choice trials than were dull males, and both age classes of bright males obtained higher quality mates earlier in the breeding season than did dull males, when nesting success was higher. In conclusion, although it appears that bright plumage increases access to higher quality mates, age also plays a central role in determining a male's overall reproductive success because of the high levels of sexual promiscuity exhibited by the red-backed fairy-wren.     

Trade-offs between postcopulatory riding and mate location in the blue milkweed beetle

In the blue milkweed beetle, Chrysochus cobaltinus (Coleoptera:Chrysomelidae), males remain stationary on females' backs forprolonged periods after a single, brief copulation. Lone malesoften attack pairs, and takeovers, in which rival males replacethe resident on the female's back, are common. I used removalexperiments to measure the effect of postcopulatory riding onlatency to remating. Females whose males were removed were morelikely to remate in the next 2 h than females that were allowedto remain paired. When females were removed, males were alsomore likely to remate in the 2-h period following removal thanwere males allowed to continue riding. This indicates that malesdelay remating by their mates at the expense of mating opportunitieswith additional females. The predicted reproductive successof guarding and nonguarding males was calculated using a modelbased upon experimentally derived latencies to remating andsimulated levels of last male paternity. Guarders outperformednonguarders when the proportion of offspring sired by the lastmale (P₂) was 0.4 or greater. Data on survival and lifetimemating success were used to evaluate survival trade-offs ofpostcopulatory riding. Although males sacrificed feeding timeto ride on females' backs, there was a positive relationshipbetween the proportion of time males spent riding and theirlongevity in the patch. These results indicate that postcopulatoryriding has no survival costs and indicate that postcopulatoryriding can be an effective paternity assurance mechanism evenwhen takeovers are common.     

Effect of alarm calling by male Red‐winged Blackbirds on nestling begging and female provisioning behavior

ABSTRACT Nestling begging and parental provisioning can attract nest predators and reduce reproductive success, so parents and their offspring might be expected to respond adaptively by minimizing predator‐attracting cues when predators threaten nests. Male Red‐winged Blackbirds (Agelaius phoeniceus) are well known for their antipredator alarm calls that contain information about the approach of potential nest predators. We examined the begging behavior of nestlings and the provisioning behavior of females in response to antipredator alarm calls of males to test the adaptive response hypothesis. Playback experiments provided no evidence that alarm calls function to switch off vocal begging; nestlings were equally likely to beg vocally during playback and control periods. Video recordings showed that male alarm calling had no significant effect on inappropriate vocal begging (in the absence of an adult), but significantly reduced the incidence of spontaneous calling (in the absence of begging). Adult females responded to male antipredator alarm calls by delaying their provisioning visits. In addition, although having no significant effect on use of nest‐arriving calls by females, male alarm calling significantly reduced their use of nest‐leaving calls. We conclude that nestling and female Red‐winged Blackbirds respond to male alarm calls in ways that might reduce the risk of predation, but nestlings beg vocally when females arrive to feed them, regardless of male alarm calling, perhaps to avoid a competitive disadvantage with broodmates.     

Experimental evidence that brighter males sire more extra‐pair young in tree swallows

Across taxa, extra‐pair mating is widespread among socially monogamous species, but few studies have identified male ornamental traits associated with extra‐pair mating success, and even fewer studies have experimentally manipulated male traits to determine whether they are related directly to paternity. As a consequence, there is little experimental evidence to support the widespread hypothesis that females choose more ornamented males as extra‐pair mates. Here, we conducted an experimental study of the relationship between male plumage colour and fertilization success in tree swallows (Tachycineta bicolor), which have one of the highest levels of extra‐pair mating in birds. In this study, we experimentally dulled the bright blue plumage on the back of males (with nontoxic ink markers) early in the breeding season prior to most mating. Compared with control males, dulled males sired fewer extra‐pair young, and, as a result, fewer young overall. Among untreated males, brighter blue males also sired more extra‐pair young, and in paired comparisons, extra‐pair sires had brighter blue plumage than the within‐pair male they cuckolded. These results, together with previous work on tree swallows, suggest that extra‐pair mating behaviour is driven by benefits to both males and females.     

Mate guarding in the Seychelles warbler is energetically costly and adjusted to paternity risk

Males may increase their fitness through extra-pair copulations (copulations outside the pair bond) that result in extra-pair fertilizations, but also risk lost paternity when they leave their own mate unguarded. The fitness costs of cuckoldry for Seychelles warblers (Acrocephalus sechellensis) are considerable because warblers have a single-egg clutch and, given the short breeding season, no time for a successful replacement clutch. Neighbouring males are the primary threat to a male's genetic paternity. Males minimize their loss of paternity by guarding their mates to prevent them from having extra-pair copulations during their fertile period. Here, I provide experimental evidence that mate-guarding behaviour is energetically costly and that the expression of this trade-off is adjusted to paternity risk (local male density). Free-living males that were induced to reduce mate guarding spent significantly more time foraging and gained significantly better body condition than control males. The larger the reduction in mate guarding, the more pronounced was the increase in foraging and body condition (accounting for food availability). An experimental increase in paternity risk resulted in an increase in mate-guarding intensity and a decrease in foraging and body condition, and vice versa. This is examined using both cross-sectional and longitudinal data. This study on the Seychelles warbler offers experimental evidence that mate guarding is energetically costly and adjusted to paternity risk.     

Copulation behaviour in mammals: evidence that sperm competition is widespread

We review information on copulation behaviour and sperm competition in mammals using data primarily from the literature. Female mammals of many species regularly copulate with more than one male during each oestrous period. Such multi-male copulations are reported more often in social, compared with solitary species. In addition, the mates of males of polygynous species experience multi-male copulations as often as the mates of males or monogamous species. Male mammals attempt to increase their certainty of paternity through a number of reproductive tactics. Copulation frequency is higher in specks with multi-male copulations compared with other species. Consortships, which can br regarded as a form of mate guarding, are often absent from species in which more than one male copulates with each female during her oestrous period. Most solitary burrow-living small mammal species copulate in the open, whereas social species often copulate inside their burrows. Insurance copulations may occur in many species since high copulation rates occur in four circumstances: (i) when mates are reunited, (ii) when a new male takes over a female, (iii) when a strange male steals a copulation, and (iv) when an audience of males is present.     

A mutual understanding? Interspecific responses by birds to each other's aerial alarm calls

Individuals are likely to benefit from responding to the alarmsignals of other species with similar predators, and mutualinterspecific responses to aerial (hawk) alarms are thoughtto be common in birds, in part because similarity in alarm callstructure among species might facilitate detection or interpretation.However, there has been no test of whether interspecific responsesto aerial alarm calls can involve mutual responses between speciesand only incomplete tests of the response of any species tosuch heterospecific alarms. We describe the aerial alarm callsof white-browed scrubwrens (Sericornis frontalis) and superbfairy-wrens (Malurus cyaneus) and use a playback experimentto test for mutual responses to each other's aerial alarm calls.The 2 species occur in similar habitats and can co-occur inmixed-species flocks during the nonbreeding season. The aerialalarm calls of both species are high pitched (7 kHz) and rapidlyfrequency-modulated calls but are distinct in frequency measuresand only the scrubwren's call had 2 parallel sounds. Both speciesfled to cover after playback of either their own or the otherspecies' alarm calls but never to control sounds. The responseto either species' alarm was almost invariant in both speciesin an experiment at high natural amplitude, but there was aslightly lower response to heterospecific compared with conspecificalarms when playbacks were at the mean natural amplitude. Ourresults demonstrate, after at least 50 years of interest inthe subject, that there can be mutual responses to aerial alarmcalls between species.