Falling out of the host nest: an overlooked factor decreasing survival of brood parasite chicks

2020 ◽  
Vol 51 (8) ◽  
Author(s):  
Marcel Honza ◽  
Miroslav Capek ◽  
Václav Jelínek ◽  
Michal Šulc
Keyword(s):  
2011 ◽  
Vol 89 (12) ◽  
pp. 1237-1248 ◽  
Author(s):  
C.B. Goguen ◽  
D.R. Curson ◽  
N.E. Mathews

The Brown-headed Cowbird ( Molothrus ater (Boddaert, 1783)) is a generalist brood parasite that often lays into nests that contain conspecific eggs. Although it has often been assumed that this multiple parasitism reduces Cowbird survival, this has rarely been evaluated. We measured Cowbird survival in nests of the Blue-gray Gnatcatcher ( Polioptila caerulea (L., 1766)), Plumbeous Vireo ( Vireo plumbeus Coues, 1866), and Western Tanager ( Piranga ludoviciana (A. Wilson, 1811)) in New Mexico, USA. Our objectives were to measure the costs of intraspecific competition on Cowbird survival in multiply-parasitized nests, evaluate if these costs were related to host size, and to compare the costs of multiple parasitism relative to other mortality sources that occur over the entire nesting cycle. Intraspecific competition reduced Cowbird survival during the nestling period in nests of all three hosts, and was of particular importance in nests of the two smaller hosts. When all sources of egg mortality were considered, however, the costs of multiple parasitism were small compared with the large effects of predation and nest desertion. Given that multiple parasitism reduces Cowbird egg survival, it is unclear why Cowbirds multiply-parasitize. Possible explanations depend on an improved understanding of fecundity and level of host nest selectivity by female Cowbirds.


2013 ◽  
Vol 9 (5) ◽  
pp. 20130573 ◽  
Author(s):  
Claire N. Spottiswoode

Many brood parasitic birds lay eggs that mimic their hosts' eggs in appearance. This typically arises from selection from discriminating hosts that reject eggs which differ from their own. However, selection on parasitic eggs may also arise from parasites themselves, because it should pay a laying parasitic female to detect and destroy another parasitic egg previously laid in the same host nest by a different female. In this study, I experimentally test the source of selection on greater honeyguide ( Indicator indicator ) egg size and shape, which is correlated with that of its several host species, all of which breed in dark holes. Its commonest host species did not discriminate against experimental eggs that differed from their own in size and shape, but laying female honeyguides preferentially punctured experimental eggs more than host or control eggs. This should improve offspring survival given that multiple parasitism by this species is common, and that honeyguide chicks kill all other nest occupants. Hence, selection on egg size in greater honeyguides parasitizing bee-eaters appears to be imposed not by host defences but by interference competition among parasites themselves.


2020 ◽  
Author(s):  
Canchao Yang ◽  
Jialiang Huang ◽  
Wei Liang ◽  
Anders P Møller

Abstract Antagonistic coevolution such as that between obligate brood parasites and their hosts promotes the evolution of a variety of trickeries that enhance successful rearing of their offspring. They do that by using host parental care to enhance their reproductive success, which in turn selects for host nest defenses or egg rejection. Studying these adaptations and counter-adaptations in different populations helps us to understand the complexity of coevolution between hosts and parasites. Here, we tested for anti-parasite defenses in an Asian population of magpies Pica pica, which is used as a regular host by the great spotted cuckoo Clamator glandarius in Europe. Unlike most magpie populations in Europe, cuckoo parasitism and specific anti-parasite defenses are absent from this Asian population. None of the cuckoos in the Asian population of magpies were capable of exploiting the magpies. That was due to magpies being evictors smaller than cuckoos that could not successfully utilize brood reducing hosts. Thus, the absence of cuckoo parasitism may be due to the absence of non-evictor brood parasites, while the absence of defenses is likely to be explained by the absence of coevolutionary interaction with any brood parasite in both the present and the past.


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