巢寄生行为

巢寄生是一种鸟类将卵产在其它鸟的鸟巢中,由义亲代为孵化和育雏的一种特殊的繁殖行为。照片中所示的草地鹨（Ａｎｔｈｕｓｐｒａｔｅｎｓｉｓ）喂食大杜鹃,就是一种种间巢寄生类型。大杜鹃是现有巢寄生鸟类８０多种中最典型的一种鸟,它可把卵寄生在１２５种其它鸟类的巢中。巢寄生行为表现在：宿主的选择,大杜鹃在繁殖期寻找与孵化期和育雏期相似、雏鸟食性基本相同、卵形与颜色易仿的宿主,多为雀形目鸟类。寄生时间上,大杜鹃多在宿主开始孵卵之前,乘宿主离巢外出时快速寄生产卵。巢寄生的协同进化,表现在宿主卵的形态特征上。寄生…     

大杜鹃对家燕的巢寄生

了解杜鹃(Cuculus spp.)对不同宿主鸟类的巢寄生,是研究杜鹃与其宿主之间协同进化的重要基础资料。大杜鹃(Cuculus canorus)和家燕(Hirundo rustica)分布遍及全国,且为同域分布,但两者之间的寄生现象尚未有过系统调查。2012年和2014年4~8月,对繁殖于吉林市昌邑区桦皮厂镇(34°58′44.18″N,126°13′26.83″E,海拔184 m)和海南岛的家燕种群进行调查,结果表明,吉林市昌邑区桦皮厂镇家燕种群的寄生率为2.4%(1/42),而在海南岛所调查的1 719个家燕巢未发现杜鹃寄生现象。同时在网络上搜集家燕巢寄生的报道案例,共记录到13巢家燕被大杜鹃寄生繁殖,均发生在北方的家燕种群。     

中杜鹃捕食比氏鹟莺的卵

许多杜鹃在产下寄生卵之前通常会先叼走或吃掉宿主的1~2枚卵,这说明杜鹃不仅是寄生性繁殖的鸟类,同时可能也是潜在的捕食者。关于杜鹃对其宿主巢捕食的动机,一般认为一是由于杜鹃发现宿主巢时,已不适合寄生,将其捕食或毁坏可迫使宿主重新筑巢,从而杜鹃会获得寄生机会;二则可能由于宿主识别并拒绝了寄生卵,一些杜鹃会通过捕食或破坏宿主的巢,作为对宿主的一种惩罚性报复。2015年6月,在贵州宽阔水自然保护区,通过录像首次记录到中杜鹃(Cuculus saturatus)捕食整巢比氏鹟莺(Seicercus latouchei)卵的行为,表明中杜鹃不仅是许多宿主鸟类的巢寄生者,同时也可能是其巢捕食者。     

大杜鹃在荒漠伯劳巢中寄生繁殖

2010年5～7月在安西极旱荒漠国家级自然保护区发现3巢荒漠伯劳被大杜鹃寄生,寄生率10.34%.荒漠伯劳产白色和粉红色两种颜色的卵,大杜鹃产白色寄生卵于卵色为白色的宿主巢中.寄生卵均产于6月,当月寄生率达42.86%.大杜鹃雏鸟19日龄离巢,离巢时体重66.24 g.     

北京小龙门东方中杜鹃多重寄生冕柳莺的报道

多重巢寄生是1只或多只寄生性鸟类在1个宿主巢内产2枚或多枚卵的特殊行为方式。对于雏鸟具有排他性的杜鹃而言,多重寄生被认为是种内个体之间或种间的一种竞争,但相关报道较少。通过野外观察和分子生物学检测技术,我们在北京小龙门国家森林公园确定了一个被东方中杜鹃(Cuculus optatus)多重寄生的冕柳莺(Phylloscopus coronatus)巢。     

中杜鹃在3种宿主巢中寄生繁殖

了解杜鹃对其宿主的选择和寄生情况,能为两者间的协同进化研究提供重要的基础资料。2012和2013年每年的4～8月,在贵州宽阔水国家级自然保护区对不同生境类型中的鸟巢进行搜索监测,记录到4例中杜鹃(Cuculus saturatus)寄生繁殖现象,其宿主分别是暗绿绣眼鸟(Zosterops japonicus)、棕腹柳莺(Phylloscopus subaffinis)和黄喉鹀(Emberiza elegans),其中棕腹柳莺和暗绿绣眼鸟是首次记录到被中杜鹃寄生。中杜鹃卵重(2.39±0.14)g(n=3),体积(2.24±0.18)cm3(n=3),通过T检验方法发现中杜鹃卵极显著大于暗绿绣眼鸟和棕腹柳莺卵(P0.001),同时在形状上也与两者极不相似,中杜鹃卵呈明显的长椭圆形,与黄喉鹀的卵在大小上无显著差异(P=0.1)。反射光谱的分析结果发现,寄生于不同宿主巢的中杜鹃卵在背景色和斑点上都具有一定差异,这表明中杜鹃的卵可能存在基因族群的分化。     

大杜鹃对北红尾鸲的放牧行为

在宿主的寄生防御压力下,鸟类巢寄生者通常会进化出一系列有效的寄生行为以提高其自身的繁殖适合度。以往研究发现,部分巢寄生者可能具有类似人类的"放牧"行为,即通过破坏或捕食不适合寄生的宿主巢,促使其重新筑巢以获取新的寄生机会。然而,对于其野外行为事件的报道并不多见。2018年5至8月,在贵州六枝地区,通过对宿主北红尾鸲(Phoenicurusauroreus)的巢进行录像监控,首次记录到大杜鹃(Cuculus canorus)对正在孵卵的北红尾鸲的放牧行为。进一步查阅了大杜鹃寄生系统中已有的放牧案例,说明放牧行为很可能是大杜鹃普遍采用的一种寄生策略。     

巢寄生的协同进化

巢寄生现象一直是鸟类学专家探讨的热点问题,对于协同进化的问题又有许多不同理论。从宿主的2种对待寄生卵的行为出发,对于巢寄生协同进化的各种理论做了简单的归纳。其中宿主的拒卵行为被认为是一种适应性的表现,这导致和寄生鸟的进化竞争。而对宿主接受卵的行为却有2种不同的观点,即进化滞后说和进化平衡说,这2种学说从不同的方面都能解释宿主接受卵的行为。关于巢寄生的协同进化问题还需要进一步的研究和更多的实例证明．     

八声杜鹃在两种缝叶莺巢中寄生繁殖

了解杜鹃对不同寄主的选择和利用,可为研究两者之间的协同进化提供重要基础资料。2012至2014年每年的3~6月,在广西弄岗地区共记录到3例八声杜鹃(Cacomantis merulinus)的寄生繁殖,其中,2例寄生于栗头缝叶莺(Orthotomus cuculatus)的巢(寄生率1.4%,n=142),其中2枚杜鹃卵均为白色具棕色斑点;1例寄生于黑喉缝叶莺(O.atrogularis)(寄生率10%,n=10),杜鹃卵为白色具棕色斑点。栗头缝叶莺为八声杜鹃寄主的首次报道,而两种缝叶莺均首次在中国记录到被八声杜鹃寄生。八声杜鹃的卵重为(1.45±0.09)g,卵体积为(1.46±0.07 cm3)(n=3),其卵大小和重量均显著大于栗头缝叶莺和黑喉缝叶莺的卵(t检验,P0.001)。     

三个东方大苇莺种群大杜鹃寄生率的变异

东方大苇莺Acrocephalus orientalis是大杜鹃Cuculus canorus的主要寄主之一。本文对东方大苇莺的3个地理种群进行杜鹃寄生率的时空比较。发现不同东方大苇莺种群被大杜鹃的巢寄生率在21.4%和65.5%之间,差异显著;不过,地理位置相近的两个种群在巢寄生率上则没有显著差异。另外,同一地理种群的巢寄生率年间也存在显著差异。     

Brood parasitism and egg matching in the Red-chested Cuckoo Cuculus solitarius in southern Africa

Host usage and relative rates of egg matching were investigated in the Red-chested Cuckoo Cuculus solitarius in southern Africa, using nest record cards and museum collections. Eighteen host species were found to be parasitized at varying degrees of intensity (0.14–12.5%). The most commonly recorded parasitized host, the Cape Robin Cossypha caffra , had a relatively low rate of parasitism (2.46%). The host species experiencing the most recorded pressure from parasitism was the Bearded Robin Erythropygia quadrivirgata , with 12.5% parasitism. Human perception of cuckoo/host egg matching was assessed for parasitized clutches of host species in museum egg collections. Eggs of three different cuckoo egg morphs were scored as matching those of the host species on a 1–5 scale. Perfect/good matching was recorded for eggs found in Chorister Cossypha dichroa , Heuglin's Cossypha heuglini and Natal Robins' Cossypha natalensis clutches. Poor and very poor matching was evident for cuckoo eggs found in four host species' clutches: the Cape Robin, Stonechat Saxicola torquata , Cape Rockthrush Monticola rupestris and Black Flycatcher Melaenornis pammelaina . Available evidence suggests that the Red-chested Cuckoo parasitizes hosts in a particular environment (low vegetation and trees). Good to intermediate matching was recorded with only 47% of host eggs, and with only 28.5% of Cape Robin clutches. A relatively high degree of host specificity, however, is suggested by the nest record card data, which indicate that species with large numbers of records are not those with the highest rates of parasitism.     

The effect of Jacobin Cuckoo Clamator jacobinus parasitism on the body mass and survival of young in a new host species

The southern African subspecies of Jacobin Cuckoo Clamator jacobinus serratus is a brood parasite of a range of host species. While Jacobin Cuckoos do not evict host young, previous research has found that host young rarely survive the nestling period. Here we provide the first records of Jacobin Cuckoo parasitism of a new host species, the Southern Pied Babbler Turdoides bicolor. We investigate rates of brood parasitism and the survival of host young. The Southern Pied Babbler is one of the largest recorded hosts for Jacobin Cuckoos and, unusually, we find that host young tend to survive the nestling period and maintain similar body mass to host young in unparasitized broods. However, host young were less likely to survive to independence than young raised in unparasitized nests, suggesting a post‐fledging reproductive cost to hosts.     

Molecular tracking of individual host use in the Shiny Cowbird – a generalist brood parasite

Generalist parasites exploit multiple host species at the population level, but the individual parasite's strategy may be either itself a generalist or a specialist pattern of host species use. Here, we studied the relationship between host availability and host use in the individual parasitism patterns of the Shiny Cowbird Molothrus bonariensis, a generalist avian obligate brood parasite that parasitizes an extreme range of hosts. Using five microsatellite markers and an 1120‐bp fragment of the mtDNA control region, we reconstructed full‐sibling groups from 359 cowbird eggs and chicks found in nests of the two most frequent hosts in our study area, the Chalk‐browed Mockingbird Mimus saturninus and the House Wren Troglodytes aedon. We were able to infer the laying behavior of 17 different females a posteriori and found that they were mostly faithful to a particular laying area and host species along the entire reproductive season and did not avoid using previously parasitized nests (multiple parasitism) even when other nests were available for parasitism. Moreover, we found females using the same host nest more than once (repeated parasitism), which had not been previously reported for this species. We also found few females parasitizing more than one host species. The use of an alternative host was not related to the main hosts' nest availability. Overall, female shiny cowbirds use a spatially structured and host species specific approach for parasitism, but they do so nonexclusively, resulting in both detectable levels of multiple parasitism and generalism at the level of individual parasites.     

Common Cuckoos Cuculus canorus change their nest‐searching strategy according to the number of available host nests

In recent decades, numerous studies have examined factors affecting risk of host nest parasitism in well‐known avian host–parasite systems; however, little attention has been paid to the role of host nest availability. In accordance with other studies, we found that nest visibility, reed density and timing of breeding predicted brood parasitism of Great Reed Warblers Acrocephalus arundinaceus by the Common Cuckoo Cuculus canorus. More interestingly, hosts had a greater chance of escaping brood parasitism if nesting was synchronized. Cuckoo nest searching was governed primarily by nest visibility at high host‐nest density. However, even well‐concealed nests were likely to be parasitized during periods when just a few hosts were laying eggs, suggesting that Cuckoos adjust their nest‐searching strategy in relation to the availability of host nests. Our results demonstrate that host vulnerability to brood parasitism varies temporally and that Cuckoo females are able to optimize their nest‐searching strategy. Moreover, our study indicated that Cuckoos always manage to find at least some nests to parasitize. Thus, in this case, the co‐evolutionary arms race should take place mainly in the form of parasitic egg rejection rather than via frontline pre‐parasitism defence.     

SOME NOTES ON THE BREEDING BIOLOGY OF THE STRIPED CUCKOO

Steyn, P. 1973. Some notes on the breeding biology of the Striped Cuckoo. Ostrich 44: 163–169.

Information is presented on the breeding biology of the Striped Cuckoo, a species for which little authentic material exists. A number of cases of parasitism of the Arrow-marked Babbler are given. Pre-laying behaviour is similar to that of the Jacobin Cuckoo. The blue egg of the cuckoo may be distinguished on several minor points, but mainly because it is rounder and broader than those of the host species. The growth and development of a nestling is outlined up to its ninth day when it was killed by a snake. It was reared to this stage with three babbler chicks, probably because several babblers contribute to feeding the nestlings. The cuckoo gains weight very rapidly, and it is suggested that this is because of its brighter gape and more intense gaping response which ensure that it is fed preferentially. Anti-predator devices such as open-gaped lunges, jerking movements of the body and the exudation of a vile-smelling brown fluid are described. The nestling cuckoo's call is identical to that of the babblers. The juvenal may be fed by its foster parents For at least 36 days after leaving the nest.     

Nest defence,enemy recognition and nest inspection behaviour of experimentally parasitized Reed Warblers Acrocephalus scirpaceus

Capsule Reed Warblers in a regularly parasitized population do not recognize Cuckoo Cuculus canorus as a special enemy and do not change their behaviour at nest immediately after being parasitized.

Aims To assess if an intruder near the nest influences the behaviour of the Cuckoo host.

Methods Host responses to Cuckoo, control Pigeon dummies and human intruder were observed. Host behaviour at 71 nests was video-recorded for 30 minutes at four experimental groups of nests: Cuckoo dummy, Cuckoo dummy + Cuckoo egg, Pigeon dummy, human intruder.

Results Reed Warblers did not respond differently to the Cuckoo and the control species. The experimental procedure had no significant effect on the behaviour of hosts during the study period. We were unable to find any differences in the time spent at the nest, clutch inspection behaviour and nest defence behaviour between morning and afternoon experimental groups. Our results do not support the hypothesis that afternoon laying by the Cuckoo is maintained by a selection pressure from the host. We observed no ejection or egg-pecking during the 30-min period after the experimental parasitism.

Conclusions Low aggression and non-specificity of host responses in our study area are in line with the fact that the Reed Warbler is an intermediate rejecter of Cuckoo eggs as expected from the spatial habitat structure hypothesis.     

Effects of Shiny Cowbird Molothrus bonariensis parasitism on different components of House Wren Troglodytes aedon reproductive success

Avian brood parasites, including cuckoos and cowbirds, have multiple negative effects on their hosts. We analysed the effects of Shiny Cowbird Molothrus bonariensis parasitism on different components (e.g. egg losses, hatching success, chick survival and nest abandonment) of House Wren Troglodytes aedon reproductive success. We also conducted an experiment to discriminate between two mechanisms that may reduce hatching success in parasitized clutches: lower efficiency of incubation due to the increase in clutch volume and disruption of host incubation by the early hatching of Cowbirds. Egg puncturing by Shiny Cowbirds reduced host clutch size at hatching by 10–20%, and parasitized nests had a decrease in hatching success of 40–80%. Egg losses and hatching failures were positively associated with the intensity of parasitism. Brood reduction was greater in parasitized nests, but the growth rate of the chicks that fledged was similar to that in unparasitized nests. The combined effects of egg losses, hatching failures and brood reduction decreased the number of fledged chicks by 80%. In addition, egg puncturing increased the likelihood of nest abandonment by Wrens. Experimental data showed that hatching failures occurred when there was a combination of: (1) an increase in the volume of the clutch by the addition of the Cowbird egg without removal of host eggs, and (2) the addition of the Cowbird egg before the onset of incubation. This was relatively common in House Wren nests, as Cowbirds generally parasitize before the onset of incubation. Our results indicate that Shiny Cowbird parasitism imposes a major impact on House Wrens, as it affects all components of the Wren's reproductive success.     

European Cuckoo Cuculus canorus parasitism and host's rejection behaviour in a heavily parasitized Great Reed Warbler Acrocephalus arundinaceus population

An unusually high frequency (64%) of European Cuckoo Cuculus canorus parasitism was found in Great Reed Warbler Acrocephalus arundinaceus clutches in central Hungary. Sixty-four per cent of the parasitized clutches contained one Cuckoo egg, 23% contained two, 10% had three and 3% had four. This means that 58% of the Cuckoo eggs were found in multiply parasitized clutches. In multiple parasitism the laying second Cuckoo removed an egg from the clutch randomly, so preferred neither the host eggs, nor the concurrent Cuckoo egg. Host response towards the parasitic eggs showed 66% acceptance, 12% ejection, 20% desertion and 2% egg burial. We found great variation in both the host and the parasitic egg colour and pattern. This reduces the chance that the parasitic egg's appearance matched that of the hosts' but, in spite of this, almost perfect mimesis was found in 28% of the Cuckoo eggs. Poorly mimetic Cuckoo eggs were more frequently rejected by Great Reed Warblers than parasite eggs that were very similar to the host eggs. This high level of mimicry sometimes makes it difficult for the observer to identify the parasitic egg, especially when it is similar in size to the host eggs. It is also difficult for the host, as shown by the relatively high recognition error and ejection cost.     

Egg morphology fails to identify nests parasitized by conspecifics in common pochard: a test based on protein fingerprinting and including female relatedness

Conspecific brood parasites lay eggs in nests of other females of the same species. A variety of methods have been developed and used to detect conspecific brood parasitism (CBP). Traditional methods may be inaccurate in detecting CBP and in revealing its true frequency. On the other hand more accurate molecular methods are expensive and time consuming. Eadie developed a method for revealing CBP based on differences in egg morphology. That method is based on Euclidean distances calculated for pairs of eggs within a clutch using standardized egg measurements (length, width and weight). We tested the applicability of this method in the common pochard Aythya ferina using nests that were identified as parasitized (39 nests) or non‐parasitized (16 nests) based on protein fingerprinting of eggs. We also analyzed whether we can distinguish between parasitic and host eggs in the nest. We found that variation in MED can be explained by parasitism but there was a huge overlap in MED between parasitized and non‐parasitized nests. MED also increased with clutch size. Using discriminant function analysis (DFA) we found that only 76.4% of nests were correctly assigned as parasitized or non‐parasitized and only 68.3% of eggs as parasitic or host eggs. Moreover we found that MED in parasitized nests increased with relatedness of the females that laid eggs in the nest. This finding was supported by positive correlation between MED and estimated relatedness in female–female pairs. Although variation in egg morphology is associated with CBP, it does not provide a reliable clue for distinguishing parasitized nests from non‐parasitized nests in common pochard.