Low frequency of observed cowbird parasitism on eastern kingbirds: host rejection, effective nest defense, or parasite avoidance?

Eastern kingbird (Tyrannus tyrannus) nests rarely are parasitizedby brown-headed cowbirds (Molotrus ater). Kingbirds are oneof a dozen or so species known to eject cowbird eggs from theirnests. We hypothesized that either kingbirds eject cowbird eggsso quickly that researchers normally do not detect the eggsduring daily nest inspections, or that cowbirds avoid parasitizingkingbirds. We tested these alternative hypotheses by experimentallyintroducing real cowbird eggs into eastern kingbird nests duringthe pre-egg, early laying, late laying, and incubation stages.We recorded the interval between "parasitism" and ejection ofthe cowbird eggs. Although kingbirds ejected 87 of 88 cowbirdeggs placed in their nests, about 40% of the eggs remained innests for more than 24 h. Thus, during daily nest inspectionswe should have observed cowbird eggs if nests were parasitizedat all. In fact, we detected only one parasitized nest amongthe 402 inspected daily. The time for ejection was longest atnests parasitized early in laying, and shorter at nests parasitizedbefore and after. This variation in ejection times may reflectthe time kingbirds require to learn to recognize their own eggs.Although kingbirds defend their nests aggressively, they donot respond to female cowbirds as unique threats and do notguard their nests before sunrise when cowbirds lay. We concludethat cowbirds avoid parasitizing eastern kingbirds because theireggs most likely will be wasted. The rejection behavior persistspossibly because it is almost cost-free (a maximum of 0.07 kingbirdegg lost or damaged per cowbird egg ejected), or it evolvedin response to conspecific rather than cowbird parasitism. Foreignkingbird eggs introduced into nests at different nest stageswere ejected only during the pre-egg stage. This result supportsthe hypothesis that rejection behavior in eastern kingbirdsevolved in response to cowbird parasitism.     

Rapid increase of host defence against brood parasites in a recently parasitized area: the case of village weavers in Hispaniola

Passerine hosts of brood parasitic birds usually vary in their ability to discriminate and reject alien eggs. Two main hypotheses have been suggested to explain the persistence of acceptor individuals in species that are exploited by brood parasites. The evolutionary lag hypothesis postulates that some hosts have not yet evolved the ability to discriminate against alien eggs. Once the ability to recognize the parasitic egg has appeared by mutation, it spreads because of the selective advantage of rejection. Parasites are then selected to produce more mimetic eggs, in order to escape host discrimination, which eventually ends up in an arms race between the parasite and the host. The evolutionary equilibrium hypothesis is based on the assumption that rejection behaviour is costly in the absence of parasitism, because of recognition errors. Acceptor hosts can persist when parasitism rate fluctuates or is consistently low. Indirect evidence for costs of rejection in the absence of parasitism has been provided by Cruz and Wiley, who reported low rejection rate for a population of village weavers (Ploceus cucullatus) introduced from Africa to Hispaniola (West Indies) more than a century ago. In Africa the species is parasitized by Chrysococcyx cuckoos and shows high levels of egg discrimination. Since no brood parasite was present in Hispaniola, Cruz and Wiley suggested that rejection was selected against in the absence of parasitism due to recognition costs. Introduction of village weavers in Hispaniola, therefore, provided a unique opportunity to test the decline of an adaptation. During the past century the shiny cowbird (Molothrus bonariensis) has expanded its range-invading most of the West Indies from South America. It was first observed in Hispaniola in 1972, and it started to exploit village weavers as a host. Given that shiny cowbirds substantially reduce the reproductive success of weavers, we should expect higher rejection rates nowadays compared to those reported by Cruz and Wiley 16 years ago. In agreement with this prediction, we found a high rejection rate of cowbird model eggs (89.3%, 95% CI = 81.1 to 97.5%), moderate levels of rejection of non-mimetic weaver model eggs (67.5%, 95% CI = 52.5 to 82.5%) and rather low levels of rejection of mimetic weaver model eggs (25%, 95% CI = 4 to 46%). The rejection rate of artificial cowbird eggs has therefore increased from 13.8% (95% CI = 5 to 22.6%) to 89.3% in 16 years. To check whether this rapid increase in host resistance is compatible with a genetic microevolutionary change, we built a population dynamics model where, as an upper bound, resistance is inherited by the progeny with a probability of one. This simple model shows that observed changes of rejection rate are compatible with a genetic microevolutionary shift only under the most favourable scenario for rejecters to spread. Relaxing one or several of these assumptions (e.g. high parasitism rate, absence of rejection costs) considerably lengthens the period needed for rejecters to spread. We suggest that both genetic and learning processes might be involved in the observed changes.     

Egg Discrimination and Sex-Specific Pecking Behaviour in Parasitic Cowbirds

We studied egg‐pecking behaviour in males and females of three cowbird species: the shiny cowbird (Molothrus bonariensis), a host generalist brood parasite, the screaming cowbird (M. rufoaxillaris), a host specialist brood parasite, and the bay‐winged cowbird (Agelaioides badius), a non‐parasitic species. We conducted three experiments in which we offered each bird an artificial nest with two plaster eggs and recorded whether egg pecking occurred and the number of pecks on each egg. In expt 1, we tested if there were species and sex differences in egg‐pecking behaviour by offering the birds two spotted eggs of similar pattern. Shiny and screaming cowbirds responded in 40.3% and 44% of the trials, respectively, with females and males presenting similar levels of response. In contrast, bay‐winged cowbirds did not show any response. In expt 2, we tested if shiny cowbirds responded differentially when they faced a choice between one host and one shiny cowbird egg, while in expt 3, we tested if screaming cowbirds responded differentially when they faced a choice between one shiny and one screaming cowbird egg. Shiny cowbirds pecked preferentially host eggs while screaming cowbirds pecked more frequently shiny cowbird eggs. Our results show that egg‐pecking behaviour is present in both sexes of parasitic cowbirds, but not in non‐parasitic birds, and that parasitic cowbirds can discriminate between eggs of their own species and the eggs of their hosts or other brood parasites.     

Function of egg punctures by Shiny Cowbirds in parasitized and nonparasitized Creamy‐bellied Thrush nests

ABSTRACT Avian brood parasites usually remove or puncture host eggs. Several hypotheses have been proposed to explain the function of these behaviors. Removing or puncturing host eggs may enhance the efficiency of incubation of cowbird eggs (incubation‐efficiency hypothesis) or reduce competition for food between cowbird and host chicks in parasitized nests (competition‐reduction hypothesis) and, in nonparasitized nests, may force hosts to renest and provide cowbirds with new opportunities for parasitism when nests are too advanced to be parasitized (nest‐predation hypothesis). Puncturing eggs may also allow cowbirds to assess the development of host eggs and use this information to decide whether to parasitize a nest (test‐incubation hypothesis). From 1999 to 2002, we tested these hypotheses using a population of Creamy‐bellied Thrushes (Turdus amaurochalinus) in Argentina that was heavily parasitized by Shiny Cowbirds (Molothrus bonariensis). We found that 56 of 94 Creamy‐bellied Thrush nests (60%) found during nest building or egg laying were parasitized by Shiny Cowbirds, and the mean number of cowbird eggs per parasitized nest was 1.6 ± 0.1 (N= 54 nests). At least one thrush egg was punctured in 71% (40/56) of parasitized nests, and 42% (16/38) of nonparasitized nests. We found that cowbird hatching success did not differ among nests where zero, one, or two thrush eggs were punctured and that the proportion of egg punctures associated with parasitism decreased as incubation progressed. Thus, our results do not support the incubation‐efficiency, nest‐predation, or test‐incubation hypotheses. However, the survival of cowbird chicks in our study was negatively associated with the number of thrush chicks. Thus, our results support the competition‐reduction hypothesis, with Shiny Cowbirds reducing competition between their young and host chicks by puncturing host eggs in parasitized nests.     

BEHAVIORAL DEFENSES AGAINST AVIAN BROOD PARASITISM IN SYMPATRIC AND ALLOPATRIC HOST POPULATIONS

The brown-headed cowbird (Molothrus ater) is a widespread, obligate brood parasite of North American passerine birds. In southern Manitoba, where hosts are sympatric with cowbirds, American robins (Turdus migratorius) ejected parasitic eggs from all experimentally parasitized clutches (N = 25) and no eggs were accepted for more than four days. In contrast, robins in northern Manitoba, an area where cowbirds do not breed, accepted parasitic eggs in 33% of nests (N = 18) for at least five days. Acceptance of experimental cowbird eggs by a second host, the yellow warbler (Dendroica petechia), was similar in allopatric (100% of 20 nests) and sympatric (88.6% of 35 nests) populations, but models of a female cowbird elicited greater nest defense by warblers in the area of sympatry. Neither host rejected eggs of conspecifics, thus, rejection of cowbird eggs was not an epiphenomenon of conspecific brood parasitism. These results support the hypothesis that recognition of cowbirds and their eggs evolved as adaptations to counter cowbird parasitism and not some other selection pressure. The expression of anti-parasite defenses by some individuals within allopatric populations further suggests these traits may be controlled genetically but persist in such areas either through the continued introgression of rejecter genes from sympatric populations or because of the low cost of rejection behavior when parasitism is absent or rare.     

Brood parasite eggs enhance egg survivorship in a multiply parasitized host

Despite the costs to avian parents of rearing brood parasitic offspring, many species do not reject foreign eggs from their nests. We show that where multiple parasitism occurs, rejection itself can be costly, by increasing the risk of host egg loss during subsequent parasite attacks. Chalk-browed mockingbirds (Mimus saturninus) are heavily parasitized by shiny cowbirds (Molothrus bonariensis), which also puncture eggs in host nests. Mockingbirds struggle to prevent cowbirds puncturing and laying, but seldom remove cowbird eggs once laid. We filmed cowbird visits to nests with manipulated clutch compositions and found that mockingbird eggs were more likely to escape puncture the more cowbird eggs accompanied them in the clutch. A Monte Carlo simulation of this 'dilution effect', comparing virtual hosts that systematically either reject or accept parasite eggs, shows that acceptors enjoy higher egg survivorship than rejecters in host populations where multiple parasitism occurs. For mockingbirds or other hosts in which host nestlings fare well in parasitized broods, this benefit might be sufficient to offset the fitness cost of rearing parasite chicks, making egg acceptance evolutionarily stable. Thus, counterintuitively, high intensities of parasitism might decrease or even reverse selection pressure for host defence via egg rejection.     

Do shiny cowbird females adjust egg pecking behavior according to the level of competition their chicks face in host nests?

Interspecific brood parasites, like the shiny cowbird (Molothrus bonariensis), lay eggs in nests of other species. Shiny cowbird females peck and puncture eggs when they parasitize host nests. This behavior increases the survival of cowbird chicks when they have to compete for food with larger nestmates. However, cowbird chicks may benefit from smaller nestmates as they increase food provisioning by parents and the cowbird chicks secure most extra provisioning. We investigated whether egg-pecking behavior by female shiny cowbirds might be adjusted to the competition that their chicks face in host nests. We found that more host eggs are destroyed per cowbird egg laid in a larger-bodied host (chalk-browed mockingbird, Mimus saturninus, 70-75 g) than a smaller-bodied host (house wrens, Troglodytes aedon, 12-13 g). We also tested egg-pecking preferences in choice experiments with female cowbirds in captivity and found cowbirds presented with eggs in artificial nests pecked first and more frequently, and punctured more frequently the larger egg when this was a host egg, but not when this was a cowbird egg. Our results are partially consistent with the hypothesis that shiny cowbird females adaptively adjust their egg pecking behavior according to the competition that their chicks face in host nests.     

Rates of parasitism,but not allocation of egg resources,vary among and within hosts of a generalist avian brood parasite

Brown-headed cowbirds (Molothrus ater) deposit their eggs into the nests of other birds, which then raise the cowbird chick. Female cowbirds thus have limited options for impacting their offspring’s development via maternal effects compared to most other passerines. Cowbirds can impact their offspring’s phenotype by choosing among potential host nests, and by adjusting egg resources based on host characteristics. To examine whether cowbirds exhibit either or both of these strategies, we investigated rates of cowbird parasitism and egg investment (egg size, yolk-to-albumen ratio, and yolk testosterone and androstenedione) among and within host species in a shrubland bird community. We found that the probability of being parasitized by cowbirds, controlling for host status as a cowbird egg accepter or rejecter and ordinal date, varied significantly among host species, indicating an apparent preference for some hosts. Parasitism rates did not differ with host size, however, and despite variation in cowbird egg size among host species, this variation was not related to host size or cowbird preference. Among host species with eggs that are larger than those of the cowbird, cowbirds were significantly more likely to parasitize nests with relatively smaller eggs, whereas parasitism rates did not vary with relative egg size in host species with smaller eggs. There was no evidence for variation in cowbird egg components among or within host species. Our data indicate that cowbirds discriminate among host nests, but do not appear to adjust the composition of their eggs based on inter- or intraspecific host variation.     

Nest desertion by a cowbird host: an antiparasite behavior or a response to egg loss?

Natural selection can favor songbirds that desert nests containingeggs of the parasitic brown-headed cowbird (Molothrus ater).However, the high variability in desertion of parasitized nestswithin species is perplexing in light of the typically highcosts of parasitism. Because nest desertion can also be a responseto partial clutch predation, we first asked if Bell's vireos(Vireo bellii) deserted nests in response to the presence ofcowbird eggs (antiparasite response hypothesis) or to egg removalby predators and female cowbirds (egg predation hypothesis).Second, we asked whether variation in nest desertion was dueto intrinsic differences among individuals or to variation innest contents. We monitored a large number of nests (n = 494)and performed a clutch manipulation experiment to test thesehypotheses. The number of vireo eggs that remained in a nestwas a strong predictor of desertion both within and among pairs.Neither the presence of a single cowbird egg, which leads tonest failure for this host, nor the number of cowbird eggs receivedin a vireo nest influenced nest desertion. Furthermore, vireosdid not desert experimental nests when we immediately exchangedcowbird eggs for vireo eggs but deserted if we removed vireoeggs and replaced them with cowbird eggs the following morning.Desertion of parasitized nests by Bell's vireos can be almostentirely explained as a response to partial or complete clutchloss and does not appear to have been altered by selection frombrood parasitism.     

Brood parasitism by cowbirds: risks and effects on reproductive success and survival in indigo buntings

We observed brood parasitism by brown-beaded cowbirds (Molothrusater) on indigo buntings (Passerina cyanea) and estimated dieimpact of parasitism on the success of the individual buntingsin their current nests and in their future survival and reproduction.Rates of parasitism over 8 years were 26.6% in 1040 nests and19.8% in 693 nests in two areas in southern Michigan. Risk ofparasitism was high early in the season; half the bunting nestswere begun after the end of the cowbird season. Risk was independentof female age, plant containing the nest, or habitat The immediatecost of parasitism was 1.19 and 1.26 fewer buntings fledgedper nest. Bunting success was lower in parasitized nests withcowbird eggs (nests were more likely to be deserted or predated),lower when the cowbird nestling failed (nests were more likelyto be predated), and lower when the cowbird fledged (fewer buntingsfledged) compared to nonparasitized nests. Costs were due toremoval of a bunting egg when die cowbird laid its own egg andto competition for parental care of the cowbird and buntingnestlings. Buntings that fledged from nests where a cowbirdalso fledged were only 18% as likely to survive and return totheir natal area in the next year as buntings from nests wherea cowbird did not fledge. Long-term effects of cowbird parasitismon adult breeding later in the season, survival to the nextseason, and reproductive success in the next season were negligiblewhen compared between birds that reared a cowbird and birdsthat reared only a bunting brood, or between birds that wereparasitized and birds that escaped parasitism. The results indicatelittle long-term cost of brood parasitism on individual fitnessof adult buntings beyond the impact on the current nest andthe survival of buntings that fledge from it; nearly all costis to the parasitized brood.     

UV reflectance of eggs of brown-headed cowbirds (Molothrus ater) and accepter and rejecter hosts

Many hosts of obligate brood parasites accept parasitic eggs despite the high costs of parasitism. Acceptance is particularly perplexing in brown-headed cowbird (Molothrus ater) (hereafter “cowbird”) hosts because the eggs of cowbirds and most hosts do not appear to match closely in visual characteristics detectable by humans. However, recent evidence suggests that parasite and host eggs may match in their ultraviolet (UV) reflectance, undetectable by humans, and that birds may use UV signals for egg discrimination. We determined whether egg colour matching in UV reflectance separates accepters and rejecters of cowbird parasitism by comparing the total UV (300–400 nm) reflectance of the eggs of 11 host species to cowbird eggs. Eggs of three of five accepter species and five of five rejecter species differed significantly from cowbird eggs in UV reflectance. We found no significant difference in the UV reflectance of the eggs of three closely related pairs of accepter and rejecter species. There also was no significant difference in the UV reflectance of cowbird eggs laid in nests of five host species, and the UV reflectance of cowbird eggs was not significantly correlated with that of host clutches. Thus, we found no support for the UV-matching hypothesis in brown-headed cowbirds and UV reflectance does not appear to separate accepters and rejecters of parasitism. Differences in UV reflectance between cowbird and host eggs, however, provide potential cues for use in egg discrimination. Experimental testing is needed to determine the relative importance of UV reflectance compared to other visual cues.     

Fitness costs and benefits of cowbird egg ejection by gray catbirds

Gray catbirds (Dumetella carolinensis) eject over 95% of brown-headedcowbird (Molothrus ater) eggs placed into their nests. Ejectionbehavior could be maintained by selection from either: (1) cowbird parasitism, if the costs of accepting a cowbird egg outweighthe costs of ejecting it, or (2) conspecific parasitism, ifsuch parasitism occurs naturally and results in ejection. Thisstudy tested the above hypotheses by measuring the cost ofacceptance of cowbird parasitism (n= 38 experimentally introducedcowbird chicks) and of cowbird egg ejection (n = 94 experiments),as well as the frequency of natural conspecific parasitismamong 229 catbird nests observed and the frequency of conspecific egg ejection (n = 27 experiments). The conspecific parasitism hypothesis was not supported because catbirds accepted all foreignconspecific eggs placed into their nests, and no natural conspecificbrood parasitism was detected at any nests. The cowbird parasitismhypothesis was strongly supported because the cost of acceptinga cowbird chick (0.79 catbird fledglings) is much greater thanthe cost of ejecting a cowbird egg (0.0022 catbird fledglingsper ejection).     

Hatching asynchrony, nestling competition, and the cost of interspecific brood parasitism

All parental hosts of heterospecific brood parasites must paythe cost of rearing non-kin. Previous research on nest parasitismby brown-headed cowbirds (Molothrus ater) concluded that competitivesuperiority of the typically more intensively begging and largercowbird chick leads to preferential feeding by foster parentsand causes a reduction in the hosts' own brood. The larger sizeof cowbird nestlings can be the result of at least two causes:(1) cowbirds preferentially parasitize species with smallernestlings and lower growth rates; and/or (2) cowbirds hatchearlier than hosts. I estimated the cost of cowbird parasitismfor each of 29 species by calculating the difference betweenhosts' published brood sizes in nonparasitized and parasitizednests and using clutch size to standardize values. In this analysis,greater incubation length and lower adult mass, surrogate measuresof the hatching asynchrony and size difference between parasiteand hosts, were both related to greater costs of cowbird parasitismwithout bias owing to phylogeny. To establish causality, I manipulatedclutch contents of eastern phoebes (Sayornis phoebe) and examinedwhether earlier hatching by a single cowbird or phoebe egg reducesthe size of the rest of the original host brood. As predicted,greater hatching asynchrony increased the proportion of theoriginal phoebe brood that was lost. This measure of the costof parasitism was partially owing to increased hatching failureof the original eggs in asynchronous broods but was not at allrelated to the size differences of older and younger conspecificnestmates. However, proportional brood loss owing to an earlierhatching conspecific was consistently smaller than brood lossowing to asynchronous cowbirds in both naturally and experimentallyparasitized phoebe nests. These results imply that althoughhatching asynchrony is an important cause of the reduction ofhost broods in parasitized clutches, competitive features ofcowbird nestlings remain necessary to explain the full extentof hosts' reproductive costs caused by interspecific brood parasitism.     

Rejection of brood‐parasitic shiny cowbird Molothrus bonariensis nestlings by the firewood‐gatherer Anumbius annumbi?

Costs imposed by brood parasitic birds exert strong selection on their hosts to avoid parasitism. While egg rejection is a common defence, nestling rejection is rarer and less well understood. Theoretical models suggest that among non‐evicting parasites such as cowbirds nestling rejection can only evolve when levels of parasitism are high. Here we describe a possible case of early rejection of cowbird nestlings, by an infrequently parasitised host, the firewood‐gatherer Anumbius annumbi. Firewood‐gatherers accepted most shiny cowbird Molothrus bonariensis eggs despite clear differences in coloration. Cowbird eggs usually hatched 4–5 d before host eggs. All parasitic nestlings died within 48 h, and hosts continued their breeding attempts. Nestling death was most likely due to neglect since little food was found in the stomach of dead nestlings. Feeding neglect could be due to differences in visual or acoustic appearance between host and parasite hatchlings. Alternatively, hosts may refrain from feeding nestlings that hatch too early compared to their normal incubation time. At the moment our data do not allow distinction between active nestling recognition or cowbird nestling failure due to the unsuitability of the firewood‐gatherer as a host (i.e. too long incubation). Experiments are needed to tease these alternatives apart.     

Host–parasite coevolution beyond the nestling stage? Mimicry of host fledglings by the specialist screaming cowbird

Egg mimicry by obligate avian brood parasites and host rejection of non-mimetic eggs are well-known textbook examples of host-parasite coevolution. By contrast, reciprocal adaptations and counteradaptations beyond the egg stage in brood parasites and their hosts have received less attention. The screaming cowbird (Molothrus rufoaxillaris) is a specialist obligate brood parasite whose fledglings look identical to those of its primary host, the baywing (Agelaioides badius). Such a resemblance has been proposed as an adaptation in response to host discrimination against odd-looking young, but evidence supporting this idea is scarce. Here, we examined this hypothesis by comparing the survival rates of young screaming cowbirds and non-mimetic shiny cowbirds (Molothrus bonariensis) cross-fostered to baywing nests and quantifying the similarity in plumage colour and begging calls between host and cowbird fledglings. Shiny cowbirds suffered higher post-fledging mortality rates (83%) than screaming cowbirds (0%) owing to host rejection. Visual modelling revealed that screaming cowbirds, but not shiny cowbirds, were indistinguishable from host young in plumage colour. Similarly, screaming cowbirds matched baywings' begging calls more closely than shiny cowbirds. Our results strongly support the occurrence of host fledgling mimicry in screaming cowbirds and suggest a role of visual and vocal cues in fledgling discrimination by baywings.     

Temporal patterns of host availability, brown-headed cowbird brood parasitism, and parasite egg mass

I studied relationships between temporal patterns of host availability, brood parasitism, and egg mass for the parasitic brown-headed cowbird (Molothrus ater). At a study site consisting largely of edge habitat in north-eastern Illinois, I found 834 bird nests from 27 species. A total of 407 cowbird eggs and nestlings were found in these nests over three laying seasons. Nearly all (n= 379; 93%) were found in the nests of seven host species. For these species and all taken together, weekly nest availability generally decreased whereas parasitism frequency generally increased throughout the cowbird laying season, but the proportions of nests parasitized and the mean number of cowbird eggs in them did not. Additionally, no correlation was found between the proportions of nests parasitized and nest availability. Cowbird egg mass generally increased throughout the laying season, indicating that foraging conditions improved and that, early in the laying season, egg mass and quality may be less important than quantity. Consistently high weekly levels of parasitism indicate that cowbird reproduction was less limited by resources needed for egg production and more by the availability of suitable host nests. Fluctuating weekly host availabilities suggest that previously established, constant rates of cowbird egg laying would produce an excess of eggs during periods of low host availability. Further, the low frequency of parasitism (1%) of nests in stages too advanced for successful parasitism, and of abandoned nests, is consistent with the hypothesis that cowbirds' consistently high rate of egg production helps assure an egg is available when an appropriate nest is found. Frequently, nests were parasitized multiple times, raising the possibility that cowbirds were interfering with their own reproduction. A diverse host community increases the possibility that a decline of any one host species is unlikely to affect cowbird reproduction significantly. Received 11 July 1997 / Accepted: 31 March 1998     

Experimental Shifts in Intraclutch Egg Color Variation Do Not Affect Egg Rejection in a Host of a Non-Egg-Mimetic Avian Brood Parasite

Avian brood parasites lay their eggs in the nests of other birds, and impose the costs associated with rearing parasitic young onto these hosts. Many hosts of brood parasites defend against parasitism by removing foreign eggs from the nest. In systems where parasitic eggs mimic host eggs in coloration and patterning, extensive intraclutch variation in egg appearances may impair the host’s ability to recognize and reject parasitic eggs, but experimental investigation of this effect has produced conflicting results. The cognitive mechanism by which hosts recognize parasitic eggs may vary across brood parasite hosts, and this may explain variation in experimental outcome across studies investigating egg rejection in hosts of egg-mimicking brood parasites. In contrast, for hosts of non-egg-mimetic parasites, intraclutch egg color variation is not predicted to co-vary with foreign egg rejection, irrespective of cognitive mechanism. Here we tested for effects of intraclutch egg color variation in a host of nonmimetic brood parasite by manipulating egg color in American robins (Turdus migratorius), hosts of brown-headed cowbirds (Molothrus ater). We recorded robins’ behavioral responses to simulated cowbird parasitism in nests where color variation was artificially enhanced or reduced. We also quantified egg color variation within and between unmanipulated robin clutches as perceived by robins themselves using spectrophotometric measures and avian visual modeling. In unmanipulated nests, egg color varied more between than within robin clutches. As predicted, however, manipulation of color variation did not affect rejection rates. Overall, our results best support the scenario wherein egg rejection is the outcome of selective pressure by a nonmimetic brood parasite, because robins are efficient rejecters of foreign eggs, irrespective of the color variation within their own clutch.     

Small hosts infrequently disrupt laying by Brown-headed Cowbirds and Bronzed Cowbirds

ABSTRACT Brood parasites often must overcome host defenses that may include behaviors that serve other functions, such as deterrence of predators and nest attendance during laying and incubation. Host use by brood parasites may also be influenced by competitors in areas where more than one parasitic species occurs. We identified the degree to which behavior of potential hosts and potential competitors affected laying by Brown‐headed Cowbirds (Molothrus ater) and Bronzed Cowbirds (M. aeneus) at a site in south Texas where they co‐occur. We watched potential host nests during the presunrise period to record cowbird laying and document nest visitation, laying, cowbird‐host encounters, and nest attentiveness by hosts. Hosts were frequently at their nests when cowbirds laid eggs (83% of 121 watches among nests of five host species) and cowbirds regularly encountered hosts (43–74% and 40–77% of watches per species of host for Brown‐headed and Bronzed cowbirds, respectively). Host nest defense infrequently interfered with cowbird laying and cowbirds rarely interacted with one another during laying. Overall, 12% of the 42 cowbird laying attempts that elicited host nest defense failed, resulting in cowbird eggs either laid atop hosts as they sat in nests or laid outside the nest cup. We clearly documented that relatively small hosts can thwart parasitism by cowbirds. Thus, the potential for successful defense of nests should be considered when assessing the evolution of behaviors to deter the removal of host eggs by cowbirds and mechanisms leading to nest abandonment. Regarding the latter, the presence of a cowbird at a nest would be a poor indicator for parasitism as some laying attempts were thwarted and unparasitized broods were reared at those nests. Despite the potential for nest defense to affect host use by cowbirds, we did not detect an effect of nest defense. Because most host defense was ineffective, we examined hypotheses for the timing of cowbird laying and host nest attendance. Our analysis of time of day of laying by Brown‐headed Cowbirds at our site and data compiled from the literature suggests that laying time is best predicted by the time of civil twilight (first light) rather than sunrise.     

Influence of Shape on Egg Discrimination in American Robins and Gray Catbirds

The eggs of some obligate brood parasites are more spherical than the eggs of their non‐parasitic relatives and hosts, which contributes to the increased strength of their shells. We examined whether egg shape, including the more spherical shape of brown‐headed cowbird eggs (Molothrus ater), influenced egg discrimination in American robins (Turdus migratorius) and gray catbirds (Dumetella carolinensis). We added a series of artificial objects to robin and catbird nests that varied in shape from a control host egg, a rounded, cowbird‐like egg, to odd‐shaped objects. Real cowbird eggs were significantly more spherical than catbird and robin eggs, which confirmed a potential cue for egg recognition. Object shape significantly influenced the probability of rejection and time to rejection in both robins and catbirds. However, rounded eggs and spheres were rejected infrequently and at frequencies similar to control eggs. Therefore, the shape of a brood parasite's egg does not appear to influence egg discrimination in these two rejecters. Robins and catbirds rejected significantly more odd‐shaped objects than egg‐shaped objects and odd‐shaped objects were rejected significantly sooner than egg‐shaped objects. The rejection of odd‐shaped objects likely represents an expression of nest‐sanitation behaviour where debris is removed from the nest. By comparison with other studies of accepters of cowbird eggs, robins and catbirds appear to reject higher proportions of odd‐shaped objects, which suggests they may have more refined abilities to discriminate against foreign objects in their nests.     

Density-dependent habitat selection by brown-headed cowbirds (<Emphasis Type="Italic">Molothrus ater</Emphasis>) in tallgrass prairie

Local distributions of avian brood parasites among their host habitats may depend upon conspecific parasite density. We used isodar analysis to test for density-dependent habitat selection in brown-headed cowbirds (Molothrus ater) among tallgrass prairie adjacent to wooded edges, and prairie interior habitat (>100 m from wooded edges) with and without experimental perches. Eight study sites containing these three habitat treatments were established along a geographical gradient in cowbird abundance within the Flint Hills region of Eastern Kansas and Oklahoma, USA. The focal host species of our study, the dickcissel (Spiza americana), is the most abundant and preferred cowbird host in the prairie of this region. Cowbird relative abundance and cowbird:host abundance ratios were used as estimates of female cowbird density, whereas cowbird egg density was measured as parasitism frequency (percent of dickcissel nests parasitized), and parasitism intensity (number of cowbird eggs per parasitized nest). Geographical variation in cowbird abundance was independent of host abundance. Within study sites, host abundance was highest in wooded edge plots, intermediate in the experimental perch plots, and lowest in prairie interior. Cowbirds exhibited a pattern of density-dependent selection of prairie edge versus experimental perch and interior habitats. On sites where measures of cowbird density were lowest, all cowbird density estimates (female cowbirds and their eggs) were highest near (100 m) wooded edges, where host and perch availability are highest. However, as overall cowbird density increased geographically, these density estimates increased more rapidly in experimental perch plots and prairie interiors. Variation in cowbird abundance and cowbird:host ratios suggested density-dependent cowbird selection of experimental perch over prairie interior habitat, but parasitism levels on dickcissel nests were similar among these two habitats at all levels of local cowbird parasitism. The density-dependent pattern of cowbird distribution among prairie edge and interior suggested that density effects on perceived cowbird fitness are greatest at wooded edges. A positive relationship between daily nest mortality rates of parasitized nests during the nestling period with parasitism intensity levels per nest suggested a density-dependent effect on cowbird reproductive success. However, this relationship was similar among habitats, such that all habitats should have been perceived as being equally suitable to cowbirds at all densities. Other unmeasured effects on cowbird habitat suitability (e.g., reduced cowbird success in edge-dwelling host nests, cowbird despotism at edges) might have affected cowbird habitat selection. Managers attempting to minimize cowbird parasitism on sensitive cowbird hosts should consider that hosts in otherwise less-preferred cowbird habitats (e.g., habitat interiors) are at greater risk of being parasitized where cowbirds become particularly abundant.