scholarly journals Does Egg Rejection Account for the Low Incidence of Cowbird Parasitism in Chestnut-Collared Longspurs (Calcarius Ornatus)?

The Auk ◽  
2002 ◽  
Vol 119 (2) ◽  
pp. 556-560 ◽  
Author(s):  
S. K. Davis ◽  
D. R. Klippenstine ◽  
R. M. Brigham

Abstract We experimentally parasitized Chestnut-collared Longspur (Calcarius ornatus) nests with mimetic and nonmimetic Brown-headed Cowbird (Molothrus ater) eggs to determine whether the low frequency of parasitism reported for that grassland host is due to egg rejection behavior. Longspurs accepted all 23 mimetic eggs (real and wooden) and rejected 9 of 22 blue nonmimetic eggs. Our results suggest longspurs accept cowbird eggs even though they are physically capable of ejecting them from their nest. Thus, the low parasitism frequency reported for that species is not a result of egg rejection behavior, but may be due to antiparasite strategies that reduce their chances of being parasitized (e.g. nest defense behavior).

The Condor ◽  
2004 ◽  
Vol 106 (3) ◽  
pp. 580-599 ◽  
Author(s):  
Brian D. Peer ◽  
Spencer G. Sealy

AbstractWe conducted a comparative analysis of eight potential correlates of egg rejection in hosts of the parasitic Brown-headed Cowbird (Molothrus ater) to test the evolutionary equilibrium and evolutionary lag hypotheses as explanations for the acceptance of cowbird parasitism. The analyses generally supported evolutionary lag. Historic contact with cowbirds may explain why hosts that have recently come into contact with cowbirds accept parasitism, but it does not account for acceptance by hosts with long histories of contact with cowbirds. Egg predation by hosts, nest sanitation, population size, and egg appearance were not correlated with rejection. Larger species that typically build larger nests were more likely to reject. Large hosts may have been parasitized more frequently in the past, possibly due to their more easily found nests or superiority as hosts, and as a result, may have had more opportunity to evolve rejection. Rejection was also correlated with taxonomic affiliation, suggesting that once rejection evolves it is maintained, which implies that rejection is not costly and thus argues against an evolutionary equilibrium. Not surprisingly, hosts with large bills were more likely to reject. This may be a corollary of the tendency for large hosts, which tend to have larger bills, to reject. An evolutionary equilibrium may exist for hosts with eggs that resemble cowbird eggs, depending on the costs to host reproductive success and the likelihood of committing recognition errors. Nevertheless, some hosts have been in contact with cowbirds for a long time, build large nests, have large bills, have a “favorable” phylogeny, and lay eggs that differ from cowbird eggs, yet accept cowbird parasitism. Chance may play a role in the accumulation of the necessary recombinants and mutations necessary for the evolution of rejection.Factores Correlacionados con el Rechazo de Huevos por parte de Hospederos de Molothrus aterResumen. Realizamos un análisis comparativo de ocho factores que potencialmente podrían estar correlacionados con el rechazo de huevos por parte de hospederos del parásito de cría Molothrus ater para poner a prueba las hipótesis de equilibrio evolutivo y de demora en la respuesta evolutiva propuestas para explicar la aceptación del parasitismo. Los análisis generalmente apoyaron la hipótesis de la demora en la respuesta evolutiva. El contacto histórico con Molothrus podría explicar por qué hospederos que sólo recientemente han entrado en contacto con estas aves aceptan el parasitismo, pero no explica por qué hay hospederos que tienen largas historias de contacto con el parásito y aceptan ser parasitadas. La depredación de huevos por parte del hospedero, el comportamiento de aseo del nido, el tamaño poblacional y la apariencia de los huevos no estuvieron correlacionados con el rechazo de huevos parásitos. Las especies grandes, que típicamente construyen nidos más grandes, presentaron una probabilidad más alta de rechazar huevos. Los hospederos más grandes podrían haber sido parasitados más frecuentemente en el pasado, posiblemente debido a que sus nidos se encuentran con mayor facilidad o a que son mejores hospederos y, como resultado, podrían haber tenido mayores oportunidades evolutivas para desarrollar el comportamiento de rechazar huevos. El comportamiento de rechazo también estuvo correlacionado con la filiación taxonómica, lo que sugiere que una vez que éste evoluciona se mantiene, implicando que no es costoso, lo que a su vez es un argumento en contra de la hipótesis del equilibrio evolutivo. De forma poco sorprendente, los hospederos con picos grandes fueron más propensos a rechazar huevos. Esto podría ser un corolario de la tendencia de los hospederos grandes (los cuales tienden a tener picos más grandes) a rechazar huevos. Es posible que exista un equilibrio evolutivo para los casos de hospederos que tienen huevos que se asemejan a los de Molothrus, dependiendo de los costos sobre el éxito reproductivo del hospedero y la probabilidad de cometer errores de reconocimiento. Sin embargo, algunos hospederos han estado en contacto con Molothrus por períodos prolongados, construyen nidos grandes, tienen picos grandes, tienen afinidades filogenéticas “favorables” y ponen huevos que difieren de los del parásito, y aún así aceptan el parasitismo. El azar podría jugar un papel importante en la acumulación de los recombinantes y mutaciones necesarios para que el comportamiento de rechazo pueda evolucionar.


1997 ◽  
Vol 75 (2) ◽  
pp. 302-307 ◽  
Author(s):  
Stanislav Pribil ◽  
Jaroslav Picman

We tested five hypotheses that may explain why House Wren (Troglodytes aedon) nests are rarely parasitized by Brown-headed Cowbirds (Molothrus ater). House Wrens may prevent parasitism in five ways: (1) by choosing to nest in cavities with small entrances (inaccessible-entrance hypothesis), (2) by restricting the size of the entrance with nest material (nest-structure hypothesis), (3) by puncturing and ejecting parasitic eggs (puncture–ejection hypothesis), (4) by burying the parasitized clutch under a new nest (egg-burial hypothesis), or (5) by abandoning the parasitized nest altogether (nest-desertion hypothesis). We tested these hypotheses in field experiments and found that (i) female cowbirds cannot enter circular entrances smaller than 38 mm in diameter, (ii) wrens prefer cavities with small entrances (inaccessible to cowbirds) to those with large entrances (accessible to cowbirds), (iii) when forced to breed in cavities with large entrances, wrens do not reduce the entrance size with nest material, (iv) despite the unusual strength of cowbird eggs, wrens are physically capable of puncture–ejecting them, (v) wrens do not puncture–eject cowbird eggs from their own nests, (vi) wrens do not abandon parasitized nests or bury the parasitized clutches under new nests. These results are consistent with the inaccessible-entrance hypothesis. We propose that additional nesting adaptations, as well as active cowbird avoidance of House Wrens, may contribute to the low frequency of cowbird parasitism.


2016 ◽  
Vol 9 (1) ◽  
pp. 39-49 ◽  
Author(s):  
Lisa C. Carmody ◽  
Alexander Cruz ◽  
Jameson F. Chace

Some host species accept eggs from brood parasites over parts of their range and reject them in other areas representing an “evolutionary lag” in the development of rejection behavior or the loss of an adapative behavior when the selection pressure of brood parasitism is removed. Hosts may deter brood parasitism through egg rejection and aggressive nest defense behavior specifically targetting female brood parasites during the egg incubation period. In areas where parasitism frequencies are spatially and temporally variable, anti-parasite behaviors may decline as costs outweigh the benefits. Along the Colorado Front Range, American robins (Turdus migratorius) breed from low elevations where the brood parasitic Brown-headed Cowbird (Molothrus ater) is abundant to near timberline (3700 m) where cowbirds are uncommon. We tested the hypothesis that egg rejection and nest defense behaviors decline with reduced probability of parasitism. We found that robins accepted 100% of immaculate (robin-like) experimental eggs at both low and high elevations, but were more likely to reject spotted (cowbird-like) experimental eggs at low elevations than high elevations. Response to egg size was more variable than to egg color. When presented with a mount of a cowbird and Song Sparrow (Melospiza melodia) near the nest, robins responded more aggressively to cowbird models than to sparrows (control), and nest defense behavior towards cowbirds was longer and more aggressive at the lower elevation sites where cowbirds are common. These results suggest that egg rejection and nest-site aggression are costly adaptations to cowbird parasitism, and these behaviors decline when the threat of parasitism is reduced.


The Condor ◽  
2006 ◽  
Vol 108 (3) ◽  
pp. 741-745 ◽  
Author(s):  
Brian D. Peer ◽  
Lyndon R. Hawkins ◽  
Edwin P. Steinke ◽  
Patricia Blair Bollinger ◽  
Eric K. Bollinger

Abstract The relationship between the Brown-headed Cowbird (Molothrus ater) and its cavity-nesting hosts has received little attention because of the assumption that cowbirds rarely parasitize these hosts. We tested the Eastern Bluebird (Sialia sialis), a host that is sometimes heavily parasitized by cowbirds, for egg ejection behavior. Bluebirds ejected 65% of experimentally added cowbird eggs (n  =  20), but ejected no experimentally added conspecific eggs (n  =  66). This suggests that cowbird parasitism, not conspecific brood parasitism, is the selective pressure responsible for egg ejection in this species. This level of rejection may be conservative because bluebirds nest in dark cavities, which may make cowbird eggs difficult to detect by bluebirds.


Behaviour ◽  
1992 ◽  
Vol 123 (1-2) ◽  
pp. 84-105 ◽  
Author(s):  
Spencer G. Sealy ◽  
Diane L. Neudorf

AbstractFour host species of the parasitic brown-headed cowbird (Molothrus ater) were exposed to taxidermic mounts of a female cowbird, fox sparrow (Passerella iliaca), and common grackle (Quiscalus quiscula) at their nests during their egg-laying or nestling stage. Red-winged blackbirds (Agelaius phoeniceus), a species that accepts cowbird eggs laid in their nests, responded more aggressively to cowbird models early in their nesting cycle, indicating that they recognized the unique threat the cowbird posed. Gray catbirds (Dumetella carolinensis), northern orioles (Icterus galbula), and cedar waxwings (Bombycilla cedrorum) can remove cowbird eggs from their nests and for the most part they responded similarly to cowbird models and the "nonthreatening control," i.e. a fox sparrow. Cedar waxwings were nonaggressive to all the models and may rely on concealment to protect their nests from enemies. Removal of cowbird eggs by puncture ejection is more risky than grasp ejection. Despite this, orioles and waxwings (puncture ejectors) were not significantly more aggressive to cowbird models at egg laying than catbirds (grasp ejectors). Responses of the three rejector species toward the cowbird model did not change over the nesting cycle, indicating further that they do not recognize cowbirds as a unique threat. Rejector species may not recognize cowbirds because they have little experience with them. With the exception of waxwings, all of the hosts recognized the grackle as an enemy and increased their levels of defence from the laying to nestling stages. Three of the host-species did not simply respond in a generalized manner to any intruder at their nests but indeed recognized specific enemies. Considerable interspecific variability exists amongst the four species in defensive behaviours, which may reflect their different nesting habitats.


The Auk ◽  
2003 ◽  
Vol 120 (1) ◽  
pp. 138-144
Author(s):  
John L. Confer ◽  
Jeffery L. Larkin ◽  
Paul E. Allen

Abstract The recent decline of Golden-winged Warblers (Vermivora chrysoptera) correlates with the loss of suitable nesting habitat, range expansion by Blue-winged Warblers (V. pinus), and eastward expansion of Brown-headed Cowbirds (Molothrus ater). Multivariate statistics were used to examine effects of those factors on Golden-winged Warbler reproduction in north central New York. Herb and shrub cover were positively correlated with clutch size. Blue-winged Warbler proximity was negatively correlated with Golden-winged Warbler clutch size. Tree cover and perhaps herb cover, after adjusting for brood size, correlated with a reduced number of Golden-winged Warbler fledglings. Herbaceous cover correlated with a greater number of cowbird eggs in Golden-winged Warbler nests. Cowbird parasitism correlated with a reduction in the number of Golden-winged Warbler eggs incubated and proportion of incubated eggs that hatched. However, cowbird parasitism, after adjusting for brood size, did not significantly affect nestling success rate. Cowbirds parasitized 30% of Golden-winged Warbler nests, which reduced the number of Golden-winged Warblers fledged by ∼17%. Average herb and tree cover values were 69 and 22 in Golden-winged Warbler territories and 60 and 23 in Blue-winged Warbler territories, respectively, with herb cover significantly greater for Golden-winged Warblers. Territories in the earliest stages of succession used by Golden-winged Warblers supported larger clutches and a reduction in the strong, negative effect of Blue-winged Warbler proximity and an increase in the negative effect correlated with cowbirds, if cowbirds were locally abundant.


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