OBSERVATIONS ON SOME KENYA EAGLES

This paper describes the continuation of work on eagles in Embu district, Kenya, especially at Eagle Hill, which has now been under observation continuously since 1949. Observations in other parts of Kenya have been included. The ecological changes possibly affecting eagles on Eagle Hill are discussed. The population fell from a pair each of Circaetus cinereus, Aquila verreauxi, Hieraetus fasciatus spilogaster, H. dubius, Polemaetus bellicosus and Stephanoaetus coronatus in 1952 to a pair each of H. dubius, P. bellicosus and S. coronatus in 1965. Possible causes of the decline are discussed. The species of eagles are not normally aggressive to one another, in contrast to other resident species such as Falco peregrinus and Buteo rufofuscus. Although the eagles appear to be ecologically separated by food preferences and habitat this is apparently not the whole explanation for the unusual concentration of eagles on this hill. Additional breeding data are given for H.f. spilogaster, H. dubius, P. bellicosus and S. coronatus. These species rear respectively 0.56, 0.65, 0.42 and 0.44 young per pair per annum. S. coronatus breeds in alternate years and cannot breed every year because of a protracted post-fledging period in which the young is fed for up to 350 days. P. bellicosus, with about the same annual reproductive rate, does not have the same breeding rhythm. Data on reproductive rates combined with other data suggest possible life spans in the wild state of adults of H.f. spilogaster 10–11 years, H. dubius nine years, P. bellicosus 14 years, and S. coronatus 16 years. At nests of H. dubius and S. coronatus changes of mates have been recorded for 16 and 17 years respectively. In S. coronatus a change occurs about every six years and in H. dubius about every four years, indicating that S. coronatus may live about 1.5 times as long as H. dubius in the wild state. One female S. coronatus was known to live for 8.5 years as an adult. Other incomplete life spans are eight and eight years for two male S. coronatus, and eight for one female of this species. Two male H. dubius have each lived for at least eight years but no female of this species has lived for more than five years. Two proven cases of re-laying after a natural disaster are recorded, one each in H. dubius and S. coronatus. Other instances are suspected in H. dubius. The habit may be commoner than is supposed in large eagles. The history of four pairs of S. coronatus, each observed for four years or more, totalling 34 pair/ years is given. S. coronatus breeds regularly every second year unless some unusual occurrence, such as a change of mates or a failure during incubation, upsets the rhythm. S. coronatus females lay 1–2 eggs at dates varying from June–October in Kenya; breeding is not confined to the dry season. Laying dates of individual females may vary by two months between one year and another. Incubation takes 48–49 days, fledging 105–116 days. The elder of two young hatched invariably kills the younger so that no more than one young is reared. Female adults are dangerously aggressive, especially during days 30–60 of the fledging period. In 86% of cases where eggs are laid a young bird is reared. Since clutches of two in practice do not result in more than one young this represents a breeding success of 86% of the potential, a very high percentage. The sex ratio of young leaving the nest is about equal, seven males to five females, in known cases. The post-fledging period in S. coronatus is 330–350 days, and the total breeding cycle about 560 days, making it impossible for the eagles to breed every year, if they rear a young bird to independence. In the post-fledging period the young S. coronatus remains within half a mile of the nest, where it is fed by the parents, the female bringing most of the prey. The adults call to attract the young bird, which flies into the nest receiving the prey there, or rarely on a tree nearby. If the adult obtains no response from the young it may carry the prey away. Although regularly fed by its parents the young eagle kills some of its own food from at least day 61 of the period onwards, but most often in the last third of the period, being then apparently stimulated by unusual periods of privation. Almost 100% of young eagles that leave the nest are reared to independence at about 15 months old. The possible biological advantages of this protracted adolescence in survival and economy of prey are discussed. The main prey of S. coronatus is antelopes, followed by hyrax. Monkeys are rarely taken. Killing methods, times, and relations with prey are discussed. The eagles usually kill in early morning or evening, but also at other times. They may cache portions of large kills. Most prey is brought to the nest between hours 4–6 of daylight. The male S. coronatus feeds his incubating mate about once every 3–3 days. Once the young has hatched his killing rate rises to about one kill per 1.7 days. The killing rate falls slowly to one kill per two days later in the fledging period. At normal times the killing rate of adults is apparently controlled by their own appetites, and the increased killing rate of the male after hatching is an exception to this rule. During the post-fledging period the feeding rate varies from 1: 2.0 days to 1: 6.2 days, averaging 1: 3 days in 130 cases. Periods of privation may last from 5–13 days. Alternatively several kills may be brought in a day, possibly from cached portions of large kills in some cases. Long foodless periods may stimulate the young eagle to kill for itself, especially in the last third of the post-fledging period. Final independence of the young is not brought about by aggressive parental behaviour, but is probably due to increasing indifference of the young to food-bringing adults. This indifference may act as a release to the adults, breaking the rhythm of bringing food to the young, and so stimulate the onset of a new breeding cycle.     

BREEDING BIOLOGY OF THE BATELEUR

Watson, R. T. 1990. Breeding biology of the Bateleur. Ostrich 61: 13–23.

Observations were made on the breeding biology of the Bateleur Terathpoius ecaudataus between 1981 and 1984, in the central region of the Kruger Nabonal Park. Nests were uniformly distributed with a mean inter-nest distance of 5,1 km and density of 3,1 nests/100km². Single-egg clutches were laid from January to June, and laying appeared to be suressed by unusually high rainfall events. The mean productivity was 0,47 young per pair per year, an a breeding failures were mainly due to failure to lay or predation. Breeding adults chaned nest sites within their territory on average once every 2,8 years, but territories and pairs were stable from year to year. Both members of a pair put equal time into care of the young.     

The behaviour of Philanthus crabroniformis (Hymenoptera: Sphecidae)

Observations were made over a two year period on the nesting and hunting behaviour of a population of Philanthus crabroniformis Smith. Data are presented on the time and speed of provisioning, the capture of prey and the species taken, the design and location of nests, the approach to the nest with prey, and aggressive interactions between females. P. gibbosus Fabr., also nested in the same area and took much the same prey. Unlike other sympatric pairs of Philanthus which have been studied, the two species in question were not totally segregated by separate nesting seasons nor by mutually exclusive habitat preferences. One aspect of the behaviour of the two Philanthus which was highly distinctive was the manner in which prey-laden females approached their nests. Selection for divergence in approach patterns may have been exerted by miltogrammine flies, a major parasite of many digger wasps.     

THE PRESENT AND PAST DISTRIBUTION OF THE BALD IBIS IN THE PROVINCE OF THE CAPE OF GOOD HOPE

Tarboton, W. R. 1981. Cooperative breeding and group territoriality in the Black Tit. Ostrich 52:216-225.

In a small, colour-ringed population of Black Tits Parus niger in central Transvaal, 11 of 19 observed breeding units comprised pairs with one to three helper-males. These pairs and groups defended permanent territories, the size of which correlated with the size of the group. There were significantly more territorial disputes during winter when less food was available than in summer. Breeding occurred in summer and the female alone built the nest, incubated the eggs and brooded the young while they were small. During this time she was fed by the alpha male and helper males, although before egg-laying the alpha male prevented helpers from courtship-feeding her. On average, unassisted pairs reared 0,88 young/season whereas pairs with helpers reared 1,55 young/season. However the feeding rate of nestlings of pairs with helpers was not higher than that of unassisted pairs and the number of young reared per group did not correlate with the number of helpers within the group.

The helper system in Black Tits was associated with a skewed sex-ratio (1,7:1 males: females) in the adult population and the data are consistent with the “hopeful reproductive” hypothesis for cooperative breeding.     

Breeding behaviour and performance of the Knysna Warbler Bradypterus sylvaticus on the Cape Peninsula,South Africa

Three pairs of Knysna Warblers were monitored on the south-eastern slopes of Table Mountain during the 2000 breeding season. Males displayed alone on territories until the second half of August, when females arrived. Nest-building (8 days) and incubation (16 days) were undertaken entirely by the female, who was not fed on the nest by the male. Chick provisioning was done mainly by the male. Arachnids and terrestrial amphipods were the most common prey brought to chicks. The fledging period was 12 days. Modal clutch size was three eggs, and depredation rates of eggs and chicks were high. After losses, replacement clutches were laid on average 19 days later, after a new nest was built. A maximum of three clutches per pair was recorded. Of 18 eggs monitored, 28% hatched and 17% fledged, equating to a production of one fledgling per pair per year. Ten days after fledging, the entire family leaves the territory, males probably returning once young are independent. The main threats to the local populations are clearing of riparian undergrowth and management practices that impact the predators of rodents.     

THE BREEDING BEHAVIOUR OF THE RED-FOOTED BOOBY SULA SULA

The breeding behaviour of the Red-footed Booby on Tower Island, Galapagos, is described. A connection is traced between the arboreal nesting habit and the type and degree of ritualised behaviour; in general territories are large, movement relatively restricted, and territorial and intra -pair displays relatively few and undifferentiated when compared, for example, with the North Atlantic Gannet, in which the opposite conditions (dense nesting and maximal inter- and intra-pair contacts) occur. On Tower Island, 96% of the Red-footed Boobies are either brown or partly brown forms and 4% are full white forms. The adaptive significance of the polymorphism is discussed, and it is tentatively suggested that the brown form may be more nocturnal than the white. The average nest density was 0–009 pairs and the maximum density 0'053 pairs per square yard. Behaviour is considered under the headings: non-display behaviour (sunning, sleeping, etc.); behaviour with some signal value (Feather Ruffing, Wing Flicking, etc.); behaviour concerned with site establishment (fighting, agonistic displays); pair relationship (mutual displays); incubation and parental care and behaviour of the chick. Before flying from their territory Red-foots Wing Flick, a signal action which they have developed to a greater extent than other sulids. Other ritualised wing movements are rarer, possibly because they are associated largely with locomotion preceding flight, which is impracticable for the arboreal Red-foot. Sideways Headshaking, a frequent dirt-dispelling movement in the Gannet, is much reduced in the Red-foot. Correspondingly, it is much less used in Red-foot displays, whereas the Gannet incorporates it into many. Territorial fighting is relatively rare. Territorial behaviour includes Flight Circuiting over the breeding area, Wing Flailing, Jabbing, non-ritualised Menacing and Forward Head Waving (a ritualised, aggressive, site-ownership display). Appeasement displays are poorly developed, being confined in the adult to a fleeting Facing-away movement. The chick lacks Beak-hiding and the implication of this for the derivation of allied adult postures is discussed. Sky-pointing or Advertising is used by the male to attract a female (occasionally vice versa); it is also a mutual display cementing the pair bond and stimulating co-operation in coition and nest building. This unusually wide range of functions, compared with other sulids, is perhaps necessitated by this species' lack of a ritualised meeting ceremony. There is little interaction between mates and their aggressiveness to each other remains overt. A noticeable sign of fear on meeting is a marked tremoring of head and neck. One to three weeks elapsed between starting the nest and laying the egg. Nest-building movements occur commonly as conflict behaviour during sexual and agonistic encounters. Incubation (tints are lengthy (male average 58-4, female 60-7 hours, maximum 199) over the 46-day incubation period; nest relief is without ceremony. Feeding of the young, by incomplete regurgitation, averages slightly less than once per day after the young are more than a month old. Young beg distinctively and frenziedly. Parents do not at first discriminate between their own and other young, but do so vigorously when their young can fly. Similarly, young Red-foots only become hostile to other young when both are well grown and capable of intruding and stealing feeds. Flight is attained gradually by progressive wing exercising and local sallies. Free-flying young return regularly (usually daily) to the nest and are fed. Later they congregate in “clubs” and show most of the adult patterns of agonistic behaviour. The post-fledging care of the young shown by the Red-foot (and other boobies) is contrasted with the lack of it in the Gannet, and a hypothesis is suggested for this important divergence within the Sulidae.     

BREEDING BEHAVIOUR OF OSPREYS PANDION HALIAETUS IN SCOTLAND

Ospreys Pandion haliaetus nested at a site near Loch Garten, Inverness-shire continuously from 1959 to 1973. Each year the Royal Society for the Protection of Birds has organized a continuous watch on the eyrie in the breeding season. The detailed records kept of the activities of Ospreys at the nest by those participating in the watch were analysed and the results presented here. Ospreys are migratory and arrived in the breeding area in early April. Nesting material was usually added to an existing eyrie platform. The male collected more material than the female. The female lined the nest cup. The extent of nest building activity and the frequencies of mating and other activities prior to laying varied markedly from year to year. These differences may have been related to changes in the identity of the nesting female, but the birds were not individually marked. Both sexes incubated but the female took the greater share and normally incubated at night. When the young hatched they were brooded by the female. The female stayed in the vicinity of the nest for most of the time until the young fledged at about 53 days old. The male Osprey caught almost all the fish eaten by his mate and young during the breeding season. The number of fish caught per day increased markedly after the young hatched. Pike Esox lucius and Trout Salmo trutta were the main species taken, and some Rainbow Trout Salmo gairdnerii were identified. There were seasonal and diurnal changes in the size and the species composition of the catch. The effects of weather conditions on hunting are examined. The occurrence of Ospreys other than the resident birds at the nest site is described. The behaviour of another pair of Ospreys which repeatedly failed to hatch eggs is described. There was an instance of egg eating in this pair, and some differences in behaviour were found between these birds and those at Loch Garten whose breeding success was good. The breeding biology of Ospreys is compared with that of other British diurnal birds of prey. In other species the female leaves the young unguarded at some stage in the nestling period and hunts food for them, whereas female Ospreys do not usually hunt in the nesting period.     

The annual cycle and breeding behaviour of the Mauritius Fody Foudia rubra

Safford, R.J. 1997. The annual cycle and breeding behaviour of the Mauritius Fody Foudia rubra. Ostrich 68 (24): 58–67.

The Mauritius Fody Foudia rubra, a highly endangered species of weaver (Ploceidae) endemic to Mauritius, was studied from 1989–1993. The plumage, various display postures (typical of the family), and seven adult and two juvenile vocalisations are described. The diet consisted of insects, nectar and fruit. Males were in breeding plumage, and breeding took place, between late August and early April, although severe weather in February 1992 terminated breeding activity early. The species appeared to be monogamous and was suspected to maintain a long-term pair bond. Pairs occupied exclusive territories of not less than 0.9 ha. Both sexes built the nest from the outset, but only the female lined it. Between breeding attempts, some pairs habitually started but then abandoned one or more nests. Clutch sizes of two to four were recorded, three being the norm. Incubation and brooding were carried out by the female; the male joined in feeding the young after daytime brooding ceased. Juvenile dependency appeared to last around two weeks after which the young were ousted from the territory. The potential productivity of up to three broods per pair per year was not achieved by any pair studied because of poor nesting success. A complete moult followed breeding. Territorial defence continued throughout the year, and no evidence for seasonal movements was seen. Two behavioural features seem unexpected: 1) male nest invitation and nest advertisement behaviour appeared to be absent; 2) females participated from the outset of nest-building (including prospecting). These could be explained by the existence of a long-term pair bond, which needs to be confirmed but would not be surprising in a species that remains on territory all year. Hypotheses that could be tested to find a mechanism responsible for the unusual features of the fody are suggested. In comparison with other fodies studied, the breeding behaviour most resembled that of the Seychelles Fody F. sechellarum (also a monogamous, non-graminivorous omnivore that breeds in solitary pairs in evergreen forest). The annual cycle was similar to that of other native passerines and most other fody taxa.     

SOCIAL ORGANIZATION AND NEST-BUILDING IN THE FOREST WEAVER BIRDS OF THE GENUS MALIMBUS (PLOCEINAE)

A comparative study was made of social organization during breeding among the genus Malimbus. In M. nitens, the male chooses the nest site, builds the nest alone, guards the nest during incubation, and feeds the young; the female incubates, broods alone and with the male feeds the young. In M. malimbicus, the male chooses the nest site, builds the nest with the female and guards the nest; the female builds the nest with the male, but incubates alone. In M. racheliae and M. cassini, the nest is built by one female and a multi-male party of two or three. One male drives off the other males when the nest is completed. One male and one female incubate alternately. The female seems to be the leader of the building group, and works like a male. In M. coronatus, the nest is built by a mixed party of males and females (3–6 birds), all working together without any overt leadership. Only one male and one female however, incubate, brood and feed the young. In their morphology and behaviour, Malimbus spp. are close to the weaver birds of the genus Ploceus. M. nitens seems the least evolved species while M. cassini and M. coronatus are behaviourally the most evolved. In the last species, which has a very elaborate nest, the pair of breeding birds is helped by one to four other birds. These helpers are birds in full adult plumage, and are probably capable of breeding and may do so at another period in the long breeding season of at least six months.     

DIET,HOME RANGE,HUNTING AND REPRODUCTIVE BEHAVIOUR OF A PAIR OF DICKINSON'S KESTREL FALCO DZCKZNSONZ IN THE KRUGER NATIONAL PARK,SOUTH AFRICA

Summary

BENN, G.A. &; KEMP, A.C. 1995. Diet, home range, hunting and reproductive behaviour of a pair of Dickinson's Kestrel Falco dickinsoni in the Kruger National Park, South Africa. Ostrich 66: 81–91.

During July-December 1992, the diet, home range, hunting and reproductive behaviour of a pair of Dickinson's Kestrel Falco dickinsoni was recorded in the Kruger National Park, South Africa. Numerically, for both sexes combined, invertebrates formed the majority (56%) of the diet, while separately the female caught 75% and the male 49% invertebrate prey. During courtship and incubation the male supplied the female with primarily vertebrate prey and both provisioned mainly vertebrates to the nestlings (male = 80%; female = 57%). The non-breeding home range of the female was 27.8 km², and the breeding home range of the male was 26.3 km2. Both utilised their home ranges differentially, the area within a 2 km radius of the nest (12.6 km²) being used proportionally more than the remaining area. The home range of the female was compared to that of other Falco spp. and was larger than would be expected based on body weight. Perch-hunting was the only technique utilised by both sexes, with 79–80% of observed strike attempts from dead trees. During the day, the 9.emale spent 87% and the male 77% of the time perch-hunting, with respective hunting success rates of 69% and 58%. During courtship, the female spent much of her time (94%) close to the nest, where the male supplied her with prey. During incubation, the male spent 95% of his time within 2 km of the nest tree, where he hunted to supply the female with prey at a rate of 0.3 items.hr^?1 and assisted in nest defence. On occasion the male entered the nest to relieve the female, and remained in the cavity on average for 134 min (n = 5). As the young got older, the female spent less time at the nest and provisioned more items to the nestlings. Overall, there was an increase in the rate of prey provisioning to the nestlings from 0.45 items.hr^?1 (10 days old) to 0.85 items.hr^?1 (21 days old). The male initially passed prey to the female but provisioned directly to older nestlings.     

Nest opening response of the Nile crocodile Crocodylus niloticus

Observations on captive Nile crocodiles, Crocodylus niloticus confirm earlier reports on parental care of nests and of young. Male and female appear to form a pair bond after courtship, the male defending nesting territory with the female rarely leaving the nest until the sounds of the young hatching stimulate her to open the nest to release them. The female transports unhatched eggs and live young in her buccal pouch to water and establishes a nursery where the young are defended for several weeks. Experiments involving playback of distress calls by tape recorder, offering of live young and eggs to the adults, the parent opening an artificial nest and vocalisations and resultant interactions between adults and young are described.     

4. GAME RESERVES IN SOUTHERN AFRICA

Steyn, P. &; Grobler, J. H. 1981. Breeding biology of the Booted Eagle in South Africa. Ostrich 52:108-118.

The Booted Eagle Hieraaetus pennatus is a breeding visitor to the Cape Province of South Africa, wintering mostly in Namibia on present knowledge. Palaearctic birds probably also reach the Cape but arrive later. Two nests in different localities in the Cape were studied. The birds breed soon after arrival. Both sexes build the nest on a cliff ledge. Incubation, which lasts 40 days, is done mostly by the female. The female spends most of her time on the nest during the first four weeks of the nestling period, but considerably less time thereafter. The male provides nearly all the prey until near the end of the nestling period, and helps to feed the young. Details of nestling growth and behaviour and of parental care are given. The nestling period was 50 and 54 days in two cases. Post-nestling dependence is about two months. Prey preferences in the two study areas were very similar: 54% birds, 33% lizards and 13% rodents. Breeding biology in South Africa is basically the same as that of Palaearctic populations, with the main differences being the habitat and cliff nest site.     

Observations on the breeding biology of the Writhed-billed Hornbill (Aceros waldeni) in the Philippines

Summary We report on some aspects of the breeding biology of the critically endangered Writhed-billed Hornbill (Aceros waldeni) on the island of Panay, Philippines. Observations were made at three nests during 1995–1997. Walling-in of the females commenced in the first week of March. One female remained incarcerated for 77 days, two of three broods completed fledging around May 20 (1995, 1997). Details on fledging of the female and her brood and postfledging care by both parents are reported.The food of the males at two nests was ca. 98% fruits and 2% invertebrates. The plants exploited comprised at least 14 species. Over a third of the fruits delivered were figs of a small number of species.Two males had average feeding rates of 0.56 and 0.88 times per hour respectively, and fed 1 to 66 (median 8) items per feeding visit at the nest. The hourly feeding rate increased after hatching, but the composition of the diet did not change noticeably. As a rule, food items were delivered singly and, during one visit, in runs of one, or rarely up to 3, species.In the three weeks following vacation of the nest, the male appeared to be the sole food provider while the female stayed continually with the 3 young (as sentinel?) in the vicinity of the nest.The nest environs were defended by the male against Tarictic Hornbills (Penelopides panini panini). Six vocalisations of the parents are mentioned. One was used in territorial skirmishes with Tarictic Hornbills.With perhaps less than 30 pairs of the Writhed-bill surviving, the future for the species looks bleak. Only drastic conservation measures can prevent the species' demise. Some have been started by the PESCP.This paper is publication No. 11 of the Philippine Endemic Species Conservation Project (PESCP) of the Frankfurt Zoological Society.     

Predation by the grey leaf monkey (Presbytis hosei) on the contents of a Bird's nest at Mt. Kinabalu Park,Sabah

An adult male grey leaf monkey (Presbytis hosei) was observed in Mt. Kinabalu Park, Sabah, Malaysia, raiding the nest of a grey-throated babbler (Stachyris nigriceps). The monkey removed from the nest and ate at least two eggs and perhaps one young hatchling. This incident appears to be the first reported case of anyPresbytis spp. consuming animal prey.     

Brood size manipulations in Great Horned Owls Bubo virginianus: are predators food limited at the peak of prey cycles?

The reproduction of raptors strongly depends on food resources. It is unclear whether predators experience superabundant food during cyclic peaks of prey populations. In order to test this hypothesis, four pairs of Great Horned Owls Bubo virginianus with two young were subjected to brood size manipulations during high densities of cyclic Snowshoe Hare Lepus americanus populations in southwestern Yukon, Canada. Broods older than 35 days were temporarily enlarged by one, and then by two, young. No effects were observed when one owlet was added, but the addition of two young resulted in significant weight losses in manipulated broods. Females with enlarged broods moved farther from their nest sites at night, presumably reflecting increased hunting effort, and also spent less time near the nest during the day. Food additions to enlarged broods returned the parental behaviour to normal. We conclude that these large predators did not experience superabundant food at this stage of the breeding season during a peak in cyclic prey.     

OBSERVATIONS ON THE BREEDING OF THE PINK-BACKED PELICAN PELECANUS RUFESCENS

This paper summarises observations on the breeding behaviour of the Pink-backed Pelican Pelecanus rufescens at Rakewa, Nyanza Province, Kenya, where the species has bred for at least 200 years. Observations covered most of one breeding season, November 1962 to April 1963. Of at least 250 nests, 35 were closely observed. The community consisted of about 815 pelicans of which about 540 were adults. The death rate is estimated at 13% per annum and the mean life-span at about seven and a half years. The breeding site, in trees above a small swamp, is 15 miles from the favoured feeding ground. The colony is protected by local Luo people. The pelicans feed and roost mainly at the Miriu Delta, 15 miles away, travelling between the two places so high up as to be unseen. They fish in the early morning, visiting the colony to feed young mainly between 09.00 and 13.00 hrs. Once the young are large both parents roost away from the colony at the Delta. The breeding season takes place from August, towards the end of the rains, to March, at the end of the dry season. The birds breed in synchronised groups, the breeding cycle for any group occupying five months. Nuptial display is performed on the nest trees, by single pairs or small groups. Two main displays are described, “pointing” and “bill-clapping”. Mating occurs on the nest, with little preliminary display. Nests are slight stick structures, repaired from year to year, and used by other pelicans if abandoned. The clutch is normally two eggs, occasionally three. Both sexes incubate, with infrequent change-overs, for 33–35 days. The chick is first brick-red, becoming covered with white down. Feathers break through at about 12 days and have covered much of the body by 30 days. At 40 days chicks can recognise their own parent. They fly at 70–75 days. Parents feed chicks by regurgitation, sometimes into the nest. They brood them closely at first, but after 10–12 days leave them much alone. Large chicks thrust the head far into the parental gullet, and injuries result from such feeding struggles. Feeding usually occurs before mid-day, each parent normally delivering two feeds with a rest between. Curious convulsive movements of the young are probably begging displays. Forty-two young hatched in 35 nests, an average of 0.6 chicks/egg laid. The heaviest mortality among young occurred between 10–30 days when 31% of all chicks died. Young which flew were produced at the rate of 0.47/egg hatched, 0.28/egg laid, and 0.57/pair.     

OBSERVATIONS AT A NEST OF THE CUCKOO-ROLLER LEPTOSOMUS DISCOLOR

A nest-cavity with two nestlings of Leptosomus discolor, found in the Comoro Islands in October 1965, are described. This is apparently the first time that nesting has been observed. The nest was in a natural cavity in a tree growing in light secondary forest. Both nestlings still had traces of their original white down, even though they were nearly fully-feathered. Apart from two thick tufts of white down on the hind-crown, the plumage appeared very like that of the adult male. Fragments of egg-shell were found in the nest. They suggest that the original eggs were rather rounded, of a pale unmarked creamy-buff, slightly glossed, measuring about 46 ± 5 ± 37 ± 5 mm. During six hours observation at the nest the birds made five visits and brought six chameleons (no other food was seen). The female fed the young, but the male accompanied her. She did not enter the nest, except on one occasion. Details of this visit are given in full, being particularly remarkable for the tameness of the female. The threat-display of the young is described and possible predators mentioned. Several calls are described, some apparently for the first time. It seems likely that most prey is caught above ground-level. The evidence suggests that the birds are monogamous, not polyandrous as has been suggested.     

First nest descriptions,nesting biology and food habits for Bernier's Vanga,Oriolia bernieri,in Madagascar

Four nests of the rare and endemic Bernier's Vanga, Oriolia bernieri, were discovered; one in 1997, one in 1998, and two in 1999 on the Masoala Peninsula, northeastern Madagascar. At the 1998 nest, the female made 189 visits with 186 deliveries of nesting material during 34.6 h of observation. The female spent 9.2% (194.2 min) of the observation time building the nest while an immature male delivered nest material six times and spent 3.2 min at the nest placing the material. Nesting material included: 67.2% (125) decomposed root material, 24.7% (46) palm fibres, 6.5% (12) dry leaves, 1.1% (2) moss, and 0.5% (1) white plant dawn. In 41.0 h of observation during the incubation period the female incubated for 53% (21.7 h) of the time, the adult male for 32.3% (13.2 h), the immature male for 4.3% (1.8 h), and the nest was unattended for 10.4% (4.3 h). This breeding attempt foiled on day 13 of incubation when a Madagascar Harrier-Hawk, Polyboroides radiatus, ate the egg(s). At one of the 1999 nests, the incubation and nestling periods were 17 days each. Three young fledged during the middle of November. Of the 82 identified prey items recorded during the nestling period, 91% were invertebrates and 9% vertebrates. Spiders, crickets, cockroaches, and geckos represented the most numerous prey taken, totaling 77% of the identified prey.     

Parental care of kestrels living in stable and varying environmental conditions

We studied parental behaviour of two populations of Eurasian kestrels (Falco tinnunculus) living in environments with different reproductive constraints: a northern Italy population, resident, with relatively long reproductive season and almost stable prey availability, and a western Finland population, long-distance migrant, with short reproductive season and fluctuating availability of main prey (voles). The Finnish population was studied during a low vole availability year. We aimed to test the supposition that in variable environments the few pairs capable of breeding during low prey availability years show high-quality parental care. To estimate the quality of parental care in both Finnish and Italian pairs we measured the difference in the number of prey delivered by the male and by the female within each pair. The parental care, measured by that parameter, was greater among Italian pairs during both the incubation and early nestling periods. However, this was not the case in the late nestling period, when food requirements of offspring are greater. Moreover, the Finnish and Italian pairs produced about the same number of fledglings. Therefore, our data supported the initial supposition and we conclude that the few Finnish pairs capable of breeding in a low vole availability year show parental care similar to Italian pairs.     

The Feeding Behaviour of a Sit and Wait Predator Ranatra dispar (Heteroptera: Nepidae): The Effect of Prey Density and Age Structure on the Number of Prey Eaten

Functional response experiments were performed in the laboratory to examine the effect of prey density (as observed in the field) on feeding behaviour, and to measure handling-times and attack-rates for each instar and adult of Ranatra dispar Montandon (Heteroptera: Nepidae) feeding on five size-classes of its common prey, Anisops deanei Brooks (Heteroptera: Notonectidae). The most generally applicable response was the Type 2, although for both the predator fifth instar and adult female and male feeding on the two smallest prey sizes, the asymptote or plateau was not observed even at the highest prey density given. Generally, the handling-time increased as prey-size increased, and decreased as the predator size increased. The attack-rate surface was far more complex. For the first two predator instars (I and II), the maximum attack-rate occurred on the smallest prey sizes (1 and 2). The maximum attack-rate for predator instar III was almost the same for prey sizes 1 and 2, that of predator instar IV was greater for prey size 2, while in the three largest predator sizes (V, female and male), the maximum attack-rate was found for prey size 3. Predator instar V had the largest attack-rate values over all prey sizes, and both the predator adult female and male had lower attack-rates for various prey sizes than instars V, IV and, to some degree, III. The results support the suggestion that small predator instars will usually compete with large instars for prey, unless they are spatially or temporally separated. Observations in the field indicate that a distinct age-specific spatial distribution exists in R. dispar and the prey, A. deanei, with the smallest individuals being found predominantly in the shallow (littoral zone) water, while the larger individuals are found in the deeper water.