Abstract
BackgroundCo-evolutionary arms-races result in spatio-temporally dynamic relationships between interacting species, e.g., brood parasites and their avian hosts. However, majority of avian co-evolutionary studies are limited to “snap-shots” of a single breeding season in an open-nesting host. In a long-term study (11 breeding seasons), we explored a unique system between the brood parasitic common cuckoo (Cuculus canorus) and its host, the common redstart (Phoenicurus phoenicurus) which is exceptional among all cuckoo hosts due to being a cavity nester. Conditions in cavities are different from open nests, e.g., lower risks of predation, more favourable microclimate, increased risks of unsuccessful eviction of host offspring by the cuckoo nestling. Different conditions in cavities thus can be expected to shape parasite-host coevolution differently from what is typically studied in open nesting hosts.ResultsIn our highly parasitised nest-box population (32.5%, n = 569 nests) only 35.7% of cuckoo eggs were laid into the nest cup and incubated by redstarts. Host nests shifted availability to later into the breeding season from 2006 to 2016 and cuckoos followed this trend by also shifting their timing of parasitism. Although previous studies revealed that redstarts selectively eject experimental non-mimetic eggs (desertion was not a specific response to foreign eggs), the hosts never ejected naturally-laid cuckoo eggs or cuckoo eggs cross-fostered into naturally non-parasitised nests. We solve the long-standing debate about the origin of cuckoo eggs found on the nest rim: we gained the first direct video-recording evidence that eggs found on the nest rim were mislaid by parasites and not ejected by hosts. Naturally-parasitised nests were deserted more often (18.6%) than control non-parasitized nests (5.6%) or nests artificially parasitised by us (1.4%). This suggests that the sight of the laying cuckoo female is the primary cue that triggers egg rejection (by desertion) in this host. Review of data from this and other study sites (10 populations, n = 853 experiments) demonstrates high variability in rejection rates and shows that populations facing higher parasitism rates reject parasitic eggs with higher frequencies. Surprisingly, cuckoo chicks either growing solitarily or with redstart chicks did not differ in their fledging success.ConclusionsWe suggest that the redstart is an ideal model system to study the flexibility and limits of brood parasite-host co-evolution in an extreme ecological setting.Electronic supplementary materialThe online version of this article (doi:10.1186/s12862-016-0835-5) contains supplementary material, which is available to authorized users.
Highlights
Co-evolutionary arms-races result in spatio-temporally dynamic relationships between interacting species, e.g., brood parasites and their avian hosts
These experimental studies suggest that cavity nesting importantly affects cuckoo-host interactions and might shape the arms-race to an alternate trajectory that differs from that in open-nesting hosts; theoretical models might benefit from including specifics of this unique system to address the flexibility and limits of cuckoo biology
Parasitism rates did not correlate significantly with research effort which was quantified as the number of nest boxes checked per breeding season (Pearson’s r = −0.05, 95% CI = −0.63 to 0.57, p = 0.88)
Summary
Co-evolutionary arms-races result in spatio-temporally dynamic relationships between interacting species, e.g., brood parasites and their avian hosts. In a long-term study (11 breeding seasons), we explored a unique system between the brood parasitic common cuckoo (Cuculus canorus) and its host, the common redstart (Phoenicurus phoenicurus) which is exceptional among all cuckoo hosts due to being a cavity nester. In contrast to all other regular cuckoo hosts, the cuckoo race parasitising redstarts shows low eviction success [16, 21] and cuckoo chicks cohabiting with redstart chicks show low fitness [22] These experimental studies suggest that cavity nesting importantly affects cuckoo-host interactions and might shape the arms-race to an alternate trajectory that differs from that in open-nesting hosts; theoretical models might benefit from including specifics of this unique system to address the flexibility and limits of cuckoo biology. This research has far been neglected [23], partly because of the scarcity of data, especially under long-term natural non-manipulated conditions [24]
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