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1.
The brood parasitic habits of the European Cuckoo Cuculus canorus have excited wonder, disbelief and speculation since the fourth century BC. Accurate knowledge of cuckoo biology, however, accumulated only slowly and mostly since 1700. The aim of this study is to review six main topics: (1) the placement of cuckoo eggs in host nests; (2) cuckoo ‘clutch’ size; (3) cuckoo egg characteristics, mimicry and rejection; (4) choice of hosts; (5) eviction of eggs and chicks; and (6) the reasons why cuckoos are brood parasites and are incapable of rearing their own young. Early errors in reporting cuckoo biology were often a consequence of poor or incomplete observations leading to erroneous interpretations. Many of the early observers were egg collectors who focussed almost exclusively on the egg-laying period, thus ignoring cuckoo chick biology. Major landmarks in cuckoo studies included the facts that: (1) cuckoo eggs often resembled those of their hosts (1760s) and that this mimicry was adaptive (1850s); (2) hosts sometimes evicted cuckoo eggs (1770s); (3) female cuckoos laid individually distinctive eggs and that specific cuckoo gentes may exist (1850s); and (4) although well recognised that cuckoo chicks were reared alone, prior to Jenner’s work in the 1780s female cuckoo parents were thought to either eat or evict the host eggs or young. Jenner’s results was more readily accepted in Britain than in Germany. Between 1700 and 1859, cuckoo brood parasitism was difficult to reconcile with the prevalent conceptual framework of physico-theology (later known as the argument from design). Thereafter, Darwin’s idea of natural selection provided a superior conceptual framework, which in conjunction with experimental testing of specific hypotheses has continued to advance our understanding of brood parasitism. Our knowledge of cuckoo biology is far from complete, however, and we predict that continuing research often incorporating new technologies will refine and extend our understanding of the cuckoo’s extraordinary biology.  相似文献   

2.
We analysed the spatial and temporal pattern of egg laying in great spotted cuckoo females using microsatellite typing to determine parentage of the eggs and nestlings found in host (magpie) nests. The results showed that there were no exclusive laying territories in the study area. Cases of multiparasitism could be due to single females laying two or more eggs in a nest, or to several females using the same nest. In the latter case multiparasitism was due to a shortage of available host nests. We argue that the need for very large laying areas and the likely small cost of sharing parental care for chicks make the costs of defending territories higher than the benefits, which has constrained the evolution of territoriality in this species. Received: 16 March 1998 / Accepted: 15 June 1998  相似文献   

3.
Few studies have been conducted on the host defenses of insects against brood parasitism. We investigated whether the silphid beetle Ptomascopus morio, a brood parasite of related silphid species Nicrophorus concolor, can also parasitize another silphid species Nicrophorus quadripunctatus and the manner in which N. quadripunctatus defends itself against parasitism. Successful brood parasitism under natural conditions was not observed at the time of year when P. morio and N. quadripunctatus are both reproductively active. Follow-up experiments revealed that P. morio attempts to oviposit near N. quadripunctatus nests, but is rarely successful if adult hosts are present. When P. morio larvae were experimentally introduced to N. quadripunctatus broods, some P. morio larvae survived when the host and parasite larvae were at the same stage. We concluded that N. quadripunctatus defends itself against brood parasitism in two ways: (1) potential brood parasites are repelled, thus limiting their access to the resource; and (2) the young of the parasitic species are killed.  相似文献   

4.
To understand the interaction of the many contextual variablesthat affect parental behavior a number of static optimalitymodels have been developed. Among these the one by Lazarus andInglis (1986) is the only one to specifically predict the magnitudeof unshared parental investment (PI), i.e., of parental carethat carries a cost to the parent and that benefits all currentoffspring equally because it cannot be divided among them. Weinvestigated specifically how parent great tits (Parus major)gear their brood defense, a form of unshared PI, to the sizeof the brood at stake and to the risk incurred as a functionof the type of predator. The predators used were dummies ofthe great spotted woodpecker (Picoides major) and of the tawnyowl (Strix aluco). Normally, adults can approach the woodpeckerwith impunity; it had inflicted heavy losses to nestlings ofthe study populations of great tits near Wolfsburg, Lower Saxony.Parent great tits whose brood had been artificially reducedto two young responded to the dummy with less defense than dida control group with their pre-test brood size left intact.The nature of defense was qualitatively the same as that elicitedby a live woodpecker. Parents confronting the owl near theirbrood decreased their response with an artificial reductionin brood size much less. Because the owl used poses a seriousrisk to the defenders, as compared to the woodpecker, the resultlends powerful support to the "total loss" version of the modelof unshared PI; it predicts brood size to affect unshared PImore strongly when there is less risk to the parent. This interpretationis correct to the extent that one premise of the model, namelythat of uncompromised parentage, can be relaxed; great tit broodscontain a sizeable number of extrapair young. Males defendedtheir brood more strongly than did females. Sex and brood manipulationadded up linearly when affecting defense level, i.e., therewas no interaction.  相似文献   

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