Egg trait variation in a large hawk-cuckoo (Hierococcyx sparverioides) host population of Chinese babax (Babax lanceolatus)
Egg trait variation in a large hawk-cuckoo (Hierococcyx sparverioides) host population of Chinese babax (Babax lanceolatus)
复制标题
大型鹰杜鹃(Hierococcyx sparverioides)寄主巴巴克斯(Babax lanceolatus)群体的卵性状变异
DOI:
10.1111/1749-4877.12128
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发表时间:
2015
影响因子:
3.3
通讯作者:
Liang Wei
中科院分区:
文献类型:
--
作者:
Yang Canchao;Liu Yang;Liang Wei
Mutual interaction between brood parasites and their hosts is a well‐known model system for studying host–parasite coevolution. Both parties have acted reciprocally, resembling an evolutionary arms race, in which adaptations and counter‐adaptations have evolved as a result of host–parasite dynamics, such as the classical cuckoo–host system. Discrimination among parasite and cuckoo eggs and rejection of foreign eggs is regarded as an important anti‐parasitism strategy. The Chinese babax (Babax lanceolatus) is a large hawk‐cuckoo (Hierococcyx sparverioides) host distributed in southwest China. A previous study shows that the babax is an intermediate egg rejector, and most cuckoo eggs are accepted by the Chinese babax, although a small proportion of hosts reject cuckoo eggs. Interestingly, the large hawk‐cuckoo lays non‐mimetic eggs in contrast to the uniform blue eggs of babaxes. Because egg coloration is a critical cue used by host species in favor of the recognition of parasitic eggs by hosts, we used a spectrometer to quantify egg color variation to understand the differentiation in discrimination ability between the egg rejectors and acceptors. We found that the chroma of intra‐clutch variation of babax eggs was more consistent in egg rejectors than in acceptors. However, no statistical significance was found in inter‐clutch variation between these two types of hosts. Our results suggest that hosts lay eggs with a low level of intra‐clutch variation without the necessity of a high level of inter‐clutch variation simultaneously as predicted by the egg signature hypothesis. This study may further indicate that selection pressures from evolutionarily recent parasites can drive individual‐based differences in an anti‐parasitism strategy.