Brood-parasitism by the Shining Cuckoo Chrysococcyx lucidus at Kaikoura, New Zealand

For three seasons starting in 1976 I studied the breeding of Shining Cuckoos Chrysococcyx lucidus in forest near Kaikoura, New Zealand. There is no evidence that the cuckoo parasitizes any host on mainland New Zealand other than the Grey Warbler Gerygone igata. A nestling cuckoo returned to within 1 km of its natal site in a subsequent breeding season, presumably after migrating beyond New Zealand. Empirical and theoretical estimates of the area occupied by Shining Cuckoos while breeding are given. Cuckoos near Kaikoura laid during ten weeks, the modal week of laying following seven weeks after the presumed peak of arrival of birds in New Zealand. First clutches of the host escaped parasitism because they were laid before most cuckoos arrived. Parasitized clutches received one cuckoo egg which replaced a host's egg. It was laid before, just after or long after the host began incubating, and mimicry was lacking. Cuckoo eggs, which were about 8% of the adult cuckoo's weight, hatched in 14–17 days. The frequency of parasitism near Kaikoura was 55% of late clutches (n = 40).
At 3–7 days old, nestling Shining Cuckoos evicted from the nest all other contents. The nestling period was at least 19 days. Growth in weight followed a logistic curve and the equation is given. Just over half the cuckoo eggs produced fledglings. The effect of brood-parasitism on the Grey Warbler's productivity was small. Only 17% of late warbler eggs, and late eggs only, were prevented by parasitism from yielding fledglings. Late laying by some Shining Cuckoos (relative to the host's incubational cycle), and late eviction, often led to brief inter-specific competition among nestlings for food. The brief coexistence of young Warblers and Cuckoos in the nest may explain the apparent mimicry by newly-hatched Shining Cuckoos of the host's young.     

Response to a Dangerous Enemy: Should a Brood Parasite be Mobbed?

Models of a long-tailed cuckoo and a song thrush (as a control) were presented 1.5 to 3 m from the nests of whiteheads, a species that the cuckoo is known to parasitize. Tests were conducted early in incubation (days 3 to 8) and during the nestling period. Most breeding females responded to the cuckoo by remaining inconspicuous or hiding. Other members of the cooperatively breeding group mobbed the cuckoo if they saw it. This difference in behaviour resulted in differences in overall response between incubation and nestling periods; the cuckoo was only occasionally mobbed during incubation because birds other than the female rarely approached the nest, whereas the cuckoo was almost always mobbed after eggs hatched. Cuckoos benefit from group breeding by whiteheads because chicks receive more food if reared by larger groups. I suggest that inconspicuous behaviour by the female in the presence of a cuckoo results in at least two effects: first, females can determine what the intentions of the cuckoo are, particularly if it intends to lay in the nest; second, no cues about size of breeding group are given to the cuckoo. Comparisons are drawn with the recent study of PAYNE et al. (1985) on splendid wrens and Chrysococcyx cuckoos. Despite similar social behaviour, splendid wrens and whiteheads behaved differently in the presence of a cuckoo. Mobbing may not always be the most appropriate tactic when faced with a brood parasite.     

棕腹杜鹃和乌鹃的宿主新记录

正棕腹杜鹃(Hierococcyx nisicolor)和乌鹃(Surniculus lugubris)是鹃形目(Cuculiformes)杜鹃科(Cuculidae)的寄生性繁殖鸟类(郑光美2011,Dickinson et al.2013)。目前棕腹杜鹃已记录的宿主主要为鹟科(Muscicapidae)鸟类,例如北灰鹟(Muscicapa dauurica)、白腹蓝姬鹟(Cyanoptila cyanomelana)等(Payne 2005,Erritz?e et al.2012)。     

OBSERVATIONS ON THE BREEDING OF THE PIED CROW AND GREAT SPOTTED CUCKOO IN NORTHERN NIGERIA

Mundy. P. J. & Cook, A. W. 1977. Observations on the breeding of the Pied Crow and Great Spotted Cuckoo in northern Nigeria. Ostrich 48:72-84.

The breeding cycle of the Pied Crow Corvus albus was studied in 1971. The birds bred in the wet season and all of 23 pairs were single-brooded. They appeared to nest territorially, and mostly close to human habitations. Average clutch size was 4.8 eggs and the greenish eggs were either pale and lightly marked, or darker and heavily marked. The average incubation and fledging periods were 181/2 and 38 days respectively. Chicks hatched asynchronously. Five crow nests were found parasitised by the Great Spotted Cuckoo Clamator glandarius and it appeared that only one hen cuckoo was responsible. The cuckoo apparently did not remove, or even crack, host eggs. One instance of an adult cuckoo feeding a juvenile was seen. In terms of growth increments a cuckoo chick substituted for one-half a crow chick but developed faster and fledged in nearly one-half the time. The cuckoo reduced host breeding success practically to zero apparently by indirect means, which contrasts with its situation in Europe.     

Breeding biology of Coquerel’s Coua ( Coua coquereli ) in Western Madagascar

The breeding biology of the endemic Coquerel’s Coua (Coua coquereli), a non-parasitic cuckoo species for which few ecological data are available, was studied in the dry deciduous forest of western Madagascar. Nestling C. coquereli remain in the nest for only a short time after hatching. At approximately 9 days old and still unable to fly, they were observed to leave the nest and then remained on the ground where they were fed by both parents. This behaviour is probably a strategy used to reduce nestling predation.     

A comparative study of host selection in the European cuckoo Cuculus canorus

Certain kinds of hosts are commonly regarded as being more suitable than other for rearing European cuckoos (Cuculus canorus) – insectivores that lay small eggs and have open, shallow nests – although empirical tests of cuckoo host selection are lacking. We analysed host use by the European cuckoo in 72 British passerines that are potential hosts and for which there was information available on life-history variables and variables related to cuckoo-host coevolution, such as rate of parasitism, rejection rate of non-mimetic model eggs and degree of cuckoo-egg mimicry of host eggs. The relative population size of the host species affected parasitism rate most strongly, followed by relatively short duration of the nestling period, and the kind of nest, with cuckoos selecting open-nesting hosts. However, the effect of the nestling period could be related to host body size and the kind of nest used, because hole-nesting species normally have longer nestling periods than open-nesters. We re-analysed the data excluding hole nesters and corvid species (species with larger body mass), but the results remained identical. The European cuckoo may benefit from selecting hosts with short nestling periods because such hosts provide food for their nestlings at a very high rate. When only those species known as cuckoo hosts were analysed, the variable that best accounted for the parasitism rate was duration of the breeding season. Therefore, availability of potential hosts in both time and space is important for cuckoos in selecting hosts. Received: 16 July 1998 / Accepted: 27 October 1998     

THE OCCURRENCE AND SIGNIFICANCE OF ANOMALOUS REPRODUCTIVE ACTIVITIES IN TWO NORTH AMERICAN NON-PARASITIC CUCKOOS COCCYZUS SPP.

Among the unusual breeding habits of the non-parasitic Yellow-billed and Black-billed Cuckoos of North America are great variability in clutch size and rate of laying, initiation of incubation long before the clutch is complete, occasional laying in nests of other species, annual irregularity in the timing of the breeding season, and semi-nomadic post-migratory movements into breeding areas where food is abundant. These facts, in addition to their peculiar diet and the very large size of their eggs, suggest that cuckoos have extraordinary problems in obtaining adequate energy for reproduction. At Bloomington, Indiana (U.S.A.), during a 15-year period, anomalies in the reproductive activities of cuckoos were concentrated into two years in which food was abundant. This was particularly true of one of these years, when there was a vast emergence of periodical cicadas: the Yellow-billed Cuckoo advanced its normal schedule and bred during peak cicada abundance, laid unusually large clutches, and parasitized Black-billed Cuckoo nests. Some females may have resumed laying in nests in which, having already deposited clutches of normal size, they had been incubating for long periods; the alternative possibility is that there was intraspecific brood parasitism. The erratic egg-laying behaviour of these cuckoos is attributed to the evolution of mechanisms permitting very quick exploitation of a favourable feeding situation. It is suggested that reproductive behaviour has become so responsive to an abundance of food that normal ordering and integration of the stages of breeding have been lost in some females. Such a loss could be responsible for the laying of eggs in alien nests, and it may have been the antecedent of obligate brood parasitism in parasitic cuckoo species.     

Breeding success of common cuckoos Cuculus canorus parasitising four sympatric species of Acrocephalus warblers

We investigated the level of parasitism, egg mimicry and breeding success of cuckoos parasitising four sympatric species of Acrocephalus warblers in southern Moravia, Czech Republic. The parasitism rate was highest in the marsh warbler Acrocephalus palustris (44.8%) followed by great reed warbler A. arundinaceus (33.8%), sedge warbler A. schoenobaenus (26.5%) and reed warbler A. scirpaceus (11.6%). Although the cuckoo eggs showed a high level of mimicry the eggs of the marsh warbler this host species rejected 72% of the cuckoo eggs, resulting in a cuckoo breeding success of only 4.3%. Cuckoo eggs laid in great reed warbler and reed warbler nests showed a similar hatching success, but the cuckoo chicks survived better in great reed warbler nests, resulting in a breeding success of 30.4%, as compared to 16.4% in nests of the reed warbler. The relationship between the level of parasitism, host rejection of cuckoo eggs, cuckoo chick survival and breeding success is discussed for the four host species.     

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)。     

An example of character release in host selection and egg colour of cuckoos Cuculus spp. in Japan

We have studied in northern Japan the hitherto unidentified eggs of a species of cuckoo in the nests of the Bush Warbler Cettia diphone . The cuckoo in question appeared to be the Himalayan Cuckoo Cuculus saturatus which parasitizes mainly the Willow Warbler Phylloscopus occipitalis in southern Japan. The egg colour in this northern Cuckoo was chocolate-brown or orange-brown, similar to that of the Bush Warbler but unlike that of the southern Himalayan Cuckoo. Egg size was significantly larger than that of the southern Himalayan Cuckoo and instead similar to that of the Little Cuckoo C. poliocephalus which uses the same host species in southern Japan, to which the Little Cuckoo is confined. The shift in host species and egg colour in the northern Himalayan Cuckoo seems to be a case of character release in the absence of the Little Cuckoo.     

Unrealistically high costs of rejecting artificial model eggs in cuckoo Cuculus canorus hosts

Most studies that have tested the egg-recognition and egg-rejection ability of European cuckoo Cuculus canorus hosts have used artificial model eggs that are much harder than real Cuckoo eggs. Here we evaluate whether the use of such models overestimates the costs of egg rejection by hosts. We tested 17 potential cuckoo host species in south-eastern Spain with both artificial hard cuckoo-egg models and real eggs taken from a population of house sparrows Passer domesticus breeding in captivity. The puncture resistance of sparrow eggs, measured in the laboratory, was more similar to that of real cuckoo eggs than was the resistance of artificial models, although sparrow eggs were less resistant than real cuckoo eggs. Potential host species with a grasp index greater than 200 mm² did not suffer high rejection costs when rejecting hard models, probably because they are grasp ejectors. However, all species with a smaller grasp index suffered high costs when rejecting hard artificial models. For these species the frequency and magnitude of costs were significantly higher when rejecting artificial hard models than when rejecting real eggs. For some species the breakage of real eggs was quite difficult (they needed 97 to more than 4000 pecks in video-recorded ejections), and sometimes the birds suffered rejection costs. These results show that realistic estimates of the frequency and magnitude of rejection costs for hosts with small bills cannot be obtained by using artificial models, and also that for a variety of medium-sized puncture ejector species the costs when rejecting real eggs may be low.     

OBSERVATIONS ON THE BREEDING OF THE PALILA PSITT1ROSTRA BA1LLEUI OF HAWAII

The behavioural ecology and breeding biology of the endangered Palila Psittirostra bailleui was studied from 1971 to 1975. The most intensive breeding occurred from June to August, and coincided with peak production of mamane Sophora chrysophylla seeds, the bir?s major food source. The Palila was able to make adjustments in its breeding to compensate for yearly differentiation in the timing and abundance of this food supply. Sexual chasing and courtship feeding were the most frequently encountered pre-nesting behaviours. Territory was a mate-defended area, which later in the nesting sequence was confined to the nest site. A total of 26 nests was found; most were placed on larger branches of mamane trees. Nest construction occurred primarily in the morning hours and lasted up to 20 days. Both sexes took part in nest construction, albeit the male role was minimal. Unless the nest was placed in the terminal fork of a tree, it usually contained a large stick base. The modal clutch size was two; eggs were laid early in the morning and in all cases one per day. Incubation sometimes began with the first egg and lasted 15–16 days. Only the female incubated, and she covered the eggs for about 75% of the daylight hours and throughout the night. Egg hatching was asynchronous, with the first young emerging early in the morning and the second not until later that same day. Only the female brooded, and the rate declined until day 15 when essentially it stopped. Both parents fed the young by regurgitation, and the number of feedings per hour decreased slightly over the nestling period. It is thought that insects and finely masticated plant material formed the bulk of the nestling diet until about day 5 when mamane seeds became important. Helpers were found at one nest. Young developed slowly and did not leave the nest until 21–27 days old. It is believed that these prolonged nestling periods were able to evolve because of the (former) absence of ground predators. After fledging, young remained with their parents for at least 30 days. Productivity was regulated by small clutch size, low population numbers and by the length of an individual nesting sequence (in that a pair could potentially raise only one brood each year). The primary reason for the endangered status of this bird appears to be the effect of habitat alteration upon a specialist, coupled with the fact that the small effective breeding population and low dis-persability of the species may have resulted in decreased genetic fitness.     

Comparison of digestive efficiency in the parasitic great spotted cuckoo and its magpie host nestlings

Altricial nestlings are under strong selection pressures to optimize digestive efficiency because this is one of the main factors affecting nestling growth and survival. Bird species vary in their ability to assimilate different nutrients and current theory predicts that nestlings should also be able to adjust their nutritional physiology to feeding frequency. Variation in parental provisioning to nestlings would select for flexibility in nestling digestive physiology, which would allow maximization of nutrient assimilation. In the present study, by making use of a brood parasite–host study system in which great spotted cuckoo nestlings (Clamator glandarius) are reared by magpie (Pica pica) host foster parents when sharing the nest with host nestlings, we tested several predictions of the adaptive digestive efficiency paradigm. A hand‐feeding experiment was employed in which we fed both great spotted cuckoo and magpie nestlings with exactly the same diet simulating one food abundance period and one food deprivation period. The results obtained show that cuckoo nestlings ingested more food, gained significantly more weight during the abundance period, and assimilated a higher proportion of the ingested food than magpie nestlings. These results demonstrate for the first time that cuckoo nestlings enjoy digestive adaptations that favour a rapid processing of the ingested food, thereby maximizing their intake rate but without decreasing digestive efficiency. © 2013 The Linnean Society of London, Biological Journal of the Linnean Society, 2014, 111 , 280–289.     

BREEDING BIOLOGY OF THE BEARDED VULTURE IN SOUTHERN AFRICA,PART II: THE NESTLING PERIOD

Brown, C. J. 1990. Breeding biology of the Bearded Vulture in southern Africa, Part I: The nestling period. Ostrich 61: 24–32.

The nestling period of the Bearded Vulture Gypaetus barbatus in southern Africa was 124–128 days. The hatching interval between the normal two-egg. clutch was usually 3–6 days (range 2–9 days Only one nestling per clutch survived to the third day. Tittle sibling aggression and no infanticide took place, but the older nestling dominated the younger which obtained no food. For the first 40 days the nestling was closely brooded. The nest duties were evenly shared by both parents, but females brooded at night. Food was brought to the nest usually once or twice per day by both parents, and was stored behind the nest. During days 41–90 parental attendance steadily decreased. Dunng this stage the female spent more time in the nesting area (57%) and on the nest (91%) than the male. Towards the end of this stage the nestlin started to feed itself but preferred to be fed by a parent. From da 91 to first flight the nestling was left unattended and was visited by its parents only to provide food, which it fed from itself. All pars monitored (40 pair-years) attempted to breed every year. The breeding success (n = 18 pair-years) was 0,89 young fledged per pair per year.     

Constraints on host choice: why do parasitic birds rarely exploit some common potential hosts?

1. Why are some common and apparently suitable resources avoided by potential users? This interesting ecological and evolutionary conundrum is vividly illustrated by obligate brood parasites. Parasitic birds lay their eggs into nests of a wide range of host species, including many rare ones, but do not parasitize some commonly co-occurring potential hosts. 2. Attempts to explain the absence of parasitism in common potential hosts are limited and typically focused on single-factor explanations while ignoring other potential factors. We tested why thrushes Turdus spp. are extremely rarely parasitized by common cuckoos Cuculus canorus despite breeding commonly in sympatry and building the most conspicuous nests among forest-breeding passerines. 3. No single examined factor explained cuckoo avoidance of thrushes. Life-history traits of all six European thrush species and the 10 most frequently used cuckoo hosts in Europe were similar except body/egg size, nest design and nestling diet. 4. Experiments (n = 1211) in several populations across Europe showed that host defences at egg-laying and incubation stages did not account for the lack of cuckoo parasitism in thrushes. However, cross-fostering experiments disclosed that various factors during the nestling period prevent cuckoos from successfully parasitizing thrushes. Specifically, in some thrush species, the nest cup design forced cuckoo chicks to compete with host chicks with fatal consequences for the parasite. Other species were reluctant to care even for lone cuckoo chicks. 5. Importantly, in an apparently phylogenetically homogenous group of hosts, there were interspecific differences in factors responsible for the absence of cuckoo parasitism. 6. This study highlights the importance of considering multiple potential factors and their interactions for understanding absence of parasitism in potential hosts of parasitic birds. In the present study, comparative and experimental procedures are integrated, which represent a novel approach that should prove useful for the understanding of interspecific ecological relationships in general.     

A host-race of the cuckoo Cuculus canorus with nestlings attuned to the parental alarm calls of the host species

The common cuckoo has several host-specific races, each with a distinctive egg that tends to match its host's eggs. Here, we show that the host-race specializing on reed warblers also has a host-specific nestling adaptation. In playback experiments, the nestling cuckoos responded specifically to the reed warbler's distinctive 'churr' alarm (given when a predator is near the nest), by reducing begging calls (likely to betray their location) and by displaying their orange-red gape (a preparation for defence). When reed warbler-cuckoos were cross-fostered and raised by two other regular cuckoo hosts (robins or dunnocks), they did not respond to the different alarms of these new foster-parents. Instead, they retained a specific response to reed warbler alarms but, remarkably, increased both calling and gaping. This suggests innate pre-tuning to reed warbler alarms, but with exposure necessary for development of the normal silent gaping response. By contrast, cuckoo chicks of another host-race specializing on redstarts showed no response to either redstart or reed warbler alarms. If host-races are restricted to female cuckoo lineages, then chick-tuning in reed warbler-cuckoos must be under maternal control. Alternatively, some host-races might be cryptic species, not revealed by the neutral genetic markers studied so far.     

OBSERVATIONS ON THE BEHAVIOUR OF BIRDS IN SOUTHERN RHODESIA

Maclean, G. L. 1974. The breeding biology of the Rufouseared Warbler and its bearing on the genus Prinia. Ostrich 45: 9–14.

The Rufouseared Warbler Prinia pectoralis, a common species of the Kalahari scrub, nests after rain at any time of the year. Nest construction and nest sites are described. The clutch is normally three or four eggs. Incubation takes 12 to 13 days and the nestling period is 11 to 13 days. Data suggest that the Rufouseared Warbler is not a member of the genus Priniu, the generic position it currently occupies.     

SUPPLEMENTARY OBSERVATIONS ON THE BREEDING BIOLOGY OF THE BOOTED EAGLE IN SOUTHERN AFRICA

Steyn, P. & Grobler, J. H. 1985. Supplementary observations on the breeding biology of the Booted Eagle in Southern Africa. Ostrich 56:151-156

Further observations on the biology of the Booted Eagle Hieraaetus pennatus in southern Africa are presented. Several nest sites in trees are described, and details of behaviour during the incubation and early nestling period are given. The down colour of nestlings is discussed. One juvenile returned to its natal area the following breeding season. In ninepair-years the replacement rate was 1,0 young/pair/year. Prey records confirm that birds predominate. The implications of the recent discovery of breeding in mid-winter in Namibia are discussed; there may be three Booted Eagle populations in southern Africa.     

Reproductive biology of the European Cuckoo Cuculus canorus: early insights, persistent errors and the acquisition of knowledge

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.     

Aspects of breeding ecology of the eastern olivaceous warbler (Hippolais pallida)

The breeding ecology of eastern olivaceous warblers Hippolais pallida is poorly known. In this study, we provide data on nest site selection and breeding parameters of the species in a population in northwestern Bulgaria, the only one known to be regularly and heavily parasitized by the common cuckoo Cuculus canorus (hereafter cuckoo). Eastern olivaceous warblers only bred within human settlements of the study area, avoiding seemingly suitable habitat outside them. Nests were built in a wide range of plant taxa but ailanthuses Ailanthus altissima and mulberries Morus spp. were most frequently used (21%). After taking into account the availability of vegetation, there was an apparent preference for several plant taxa but not for mulberries. Mean nest height was 1.65 ± 0.98 (0.53–7.60) m, n = 217, and it varied significantly among different types of nesting substrate. Laying date and clutch size of first breeding attempts averaged 10 June ± 0.98 days, n = 101 and 3.9 ± 0.07 (2–5) eggs, n = 72, respectively. Hatching success, fledging success, and breeding success were 42.5, 86.4, and 36.7%, respectively. The main sources of nest mortality were predation and cuckoo parasitism, with no significant difference in the proportion of nests lost to each. Cuckoo parasitism seemed responsible for the relatively low hatching success in this population.