Movements and Resource Selection of Fledgling Goshawks in Montane Forests of Southeastern British Columbia

ABSTRACT The northern goshawk (Accipiter gentilis) has been the subject of considerable interest because of the impact of logging on this species' nesting habitat. However, few studies have examined movements of fledgling birds around the nest prior to independence, and even fewer have described resource requirements of young birds during their postfledging period. Over 3 years, we followed 31 radiotagged goshawk fledglings from 15 nests in southeastern British Columbia, Canada. Of these birds, 26 survived to disperse. Between fledging and dispersal 95% of fledgling relocations (n = 1, 148) were within 450 m of the nest. Fledglings primarily remained within 298 m of the nest during the first 21 days postfledging and within 525 m of the nest between 21 days postfledging and dispersal. Fledglings' movements were highly directional, with individual and sibling movements away from any particular nest tending out in one direction. Postfledging areas averaged 36.7 ha in size (median = 23.1, inter-quartile range = 20.8–39.7 ha). Fledglings strongly avoided forest <40 years old and weakly selected young forests (40–80 yr), mature forests (>80 yr), and stands with >40% canopy cover during the first 21 days and after. We suggest forest managers wishing to conserve goshawk postfledging areas in the interior montane forests of British Columbia maintain forests >40 years old with high crown closure covering an area ≥21 ha and preferably >40 ha. This area should contain all identified occupied and alternative nest trees in a nest area. At least half this area should be forest >80 years old and contain existing nests and potential for future nest trees.     

Behaviour in the post-nestling dependence period of radio-tagged Common Buzzards Buteo buteo

Behaviour of 26 young Common Buzzards Buteo buteo was studied by systematic radiotracking during July and August 1991. After hatching between 11 May and 18 June, the young buzzards fledged when they were 43–54 days old. Distances travelled from the nest increased abruptly after birds were 65 days old, when their flight feathers had completed growth: buzzards were located more than 500 m from the nest in only 2% of records within 65 days of hatching but in 26% of records when they were older. Before their 65th day, there was an increase with age in distance from the nest, time spent flying and time spent calling, especially for buzzards with continuous woodland around the nest. The increases in distance and areas covered were greatest for broods where parents were most often present, which was at nests with the most grass and arable farmland nearby. Between their 65th and 100th days, buzzards showed no increase in activity with age and called less, especially where there was extensive woodland, and travelled farthest from nests with least neighbouring grassland; broods with few young most often had parents nearby. Young buzzards associated strongly with each other between leaving the nest and completing feather growth, but some broods later became much less cohesive. Variation in activity was not linked to sex or to the presence of 30 g back-pack radio-tags compared with 12-g leg-mounted radio-tags.     

Diesj?hriger Eisvogel (Alcedo atthis) als Helfer am Nest

Summary On 24. and 26.7. 1986 a ringed first-year male kingfisher was observed carrying fish into a burrow containing nestlings 22–24 days old. The first-year bird had hatched at a breeding site 5.5 km away from the place where it helped feed the nestlings and left its own natal nest on 11.6. 1984. The first-year kingfisher's parents were not the adult birds whose nestlings the young male was feeding.     

绿鹭的繁殖习性观察

2001年4－9月在合肥市对绿鹭（Butorides striatus)的繁殖习性进行了观察。绿鹭营巢生境主要选择在建筑物附近的高大阔叶树上,常一树一巢,未见与其他鹭类混群营巢。每巢产3－5枚卵,孵卵期21d,育雏期41d,42日龄后幼鸟离巢飞走,出飞存活率62．5％。育雏期雏鸟主要食物为小型鱼类。在4所大学校园及1处公园统计到有效巢56个,推算绿鹭224只。绿鹭在合肥繁殖属首次记录。     

EDITORIAL

Olver, M. D. &; Kuyper, M. A. 1978. Breeding biology of the Whitebreasted Cormorant in Natal. Ostrich 49:25-30.

From 1972–1975 Whitebreasted Cormorants Phalacrocorax carbo bred at the Cedara Dam, Natal, South Africa (29 32S, 30 17E), and from 1973 they fished for food at Midmar Dam, 5 km away and carried the food back to the nestlings. Breeding occurred from April to October and was preceded by a period of courtship. Nesting material was collected by the males and the nests built by the females. The mean clutch size for 1972–1973 was 3,1. Both parents incubated the eggs and guarded the nest and chicks. Growth of the chicks was studied in 1972–1973. The mean number of chicks reared was 1,6 per nest although seven nests contained three nestlings. At 28 days they left the nest when alarmed, but could not fly until 49 days old. The average flying age appeared to be about 53 days. The height of the nests above the ground seemed to determine the nest leaving age. Of the 186 eggs laid in the 60 nests observed over two years, 74% hatched. Fledging success was 52% of eggs laid and 69% of eggs hatched. Chick mortality seemed to be caused mainly by falling from the nests and dying of starvation.     

THE BREEDING BEHAVIOUR AND BIOLOGY OF THE SHORT-BILLED FORM OF THE WHITE-TAILED BLACK COCKATOO CALYPTORHYNCHUS FUNEREUS

The breeding biology of the short-billed form of the White-tailed Black Cockatoo was studied at two main study areas, Coomallo Creek, an area with large tracts of uncleared lands, and Manmanning, an area of extensive clearing with little native vegetation remaining. The study was based on individually marked birds. The actions of females selecting and preparing their nest hollow ensured that other females were kept away from the area of that nest, resulting in nests being spaced out through the study areas. Eggs were laid between July and November with birds at Manmanning starting about four weeks after those at Coomallo Creek. Clutch size was a maximum of two and incubation took 28–29 days. Hatching success was higher for two-egg clutches than for one-egg clutches. There were no differences between fledging success for one-egg or two-egg clutches at either area, but fledging success at Manmanning was lower than that of Coomallo Creek. Rates of growth for weight and length of folded left wing were calculated for nestlings from both areas. These rates of growth were compared within areas between years and between areas within years. There were differences in rates of growth of nestlings from Coomallo Creek compared with those from Manmanning and these differences were related to shortages of food at Manmanning. The annual survival of tagged adults was calculated at 61–69% and that of juveniles over the first 12 months after fledging at 15%. The survival figures for adults seemed too low and it is suggested that the wearing of wing-tags may place the individual at a selective disadvantage compared with an untagged individual.     

Effects of experimental food supplementation on movements of juvenile northern goshawks (<Emphasis Type="Italic">Accipiter gentilis atricapillus</Emphasis>)

Food availability is thought to strongly influence the leaving phase of natal dispersal in animals with condition-dependent dispersal. We conducted a food supplementation experiment to determine the influence of extra food on the onset of dispersal and early dispersal movement patterns of 42 radio-tagged northern goshawks (Accipiter gentilis atricapillus) from 28 broods in north-central New Mexico during 1992 and 1993. We randomly assigned half of the broods each year as treatments and the other half as controls. Treatment broods were given supplemental food from hatching (late April) until mid-October. Control broods received the same visitation rate but no food. Birds were located approximately every 2 days from fledging until mid-October in 1992 and 1993. Timing of fledging and independence were not affected by the treatment. However, extra food significantly influenced post-fledging movements of juvenile goshawks. During the late fledgling-dependency period (>65 days of age until independence) control birds were located in the natal area (<2 km from nest tree) more frequently than supplemented birds. This pattern reversed after independence (approximately 82 days of age) when supplemented birds were located more frequently in the natal area than controls. After independence the control birds were never located in the natal area and by the end of September in both years the controls had all left the study area (study area boundaries were approximately 25 km from nest tree). Supplemented birds were never located outside of the study area for the duration of the experiment. We conclude that the control birds dispersed out of the study area and the supplemented birds remained. Since the experimentally fed juveniles remained near a known food source and the controls did not, our study demonstrates that food availability influences at least the first 4 months of post-fledging movement patterns in this population. These results also suggest individuals base dispersal decisions on knowledge of their environment at a local scale, which can influence juvenile recruitment.     

Foraging behaviour of nest predators at open-cup nests of woodland passerines

Nest predation patterns and processes cannot be understood without studying the behaviour of predators. I videotaped the behaviour of 22 species of predators at 171 depredated nests of 13 passerine species, in woodland in the Czech Republic. About 32% (60/187) of all events occurred during the night; mammals accounted for 95% (57/60) and 22% (28/127) of nocturnal and diurnal predation, respectively. About 67% (57/85) of mammalian predation, but only 3% (3/102) of avian predation, occurred during night. Multiple predations by the same species were detected in at least 7% (6/82) and 42% (37/88) of nests depredated by mammals and birds, respectively. Martens Martes martes/foina took nest content mostly all at once; birds (mainly Jay Garrulus glandarius) revisited partially depredated nest during 1–4 consecutive days. Martens stayed at the depredated nest about five times longer than Jays. Martens spent similar time at nests with eggs and nestling, while Jays stayed about twice longer at nests with eggs. Mammals consumed eggs always at the nest (23/23), but took nestlings away in at least 48% (31/64) cases. Birds took the eggs and nestling away in at least 31% (18/58) and 76% (71/94) cases, respectively. Predator visits to active nests without taking the content, repeated partial predation and revisitation of previously depredated nests suggest an effect of memory on predator’s foraging behaviour.     

Observations on the breeding biology and behaviour of the Lesser Jacana,Microparra capensis

Two Lesser Jacana nests were found in Hwange National Park, Zimbabwe and were observed over a period of four months beginning in March 2000. Both sexes were involved in preparing the breeding platform, incubation, and caring for the chicks, which were not carried by the adults. Both nests had three eggs. The incubation period for one clutch of eggs was not less than 19 days. The chicks all hatched on the same day and remained in the vicinity ofthe nest for the first few days where they were brooded by an adult. Initially the adults brought food to the chicks but the chicks started feeding themselves when they moved away from the nest. Ten days after hatching the chicks had doubled in size and were walking confidently with the attending adult some distance from the nest. First flight was seen at 32 days old, and the chicks appeared to be independent 63 days after hatching.     

BREEDING OF SACRED IBIS THRESKIORNIS AETHIOPICA AT LAKE SHALA, ETHIOPIA

Data are based on more than 200 h of observation at Ethiopia's Lake Shala from 1966 to 1972. Except for differences in size of bill, there are no useful field characters separating male and female Sacred Ibis. The breeding plumage is described; vivid blood-red colour underneath the wings and the ornamental plumes are especially obvious when nesting commences. Physical and biological features of Lake Shala, Ethiopia, and its nesting islands are described; the species of birds nesting on the Shala islands are given. Ibises nest at Shah from March to August; no nesting has been recorded from September to February during the last months of the ‘big’ rains through the main dry season. Nesting normally begins in the ‘small’ rains (between 14 March-24 April), although instances were recorded as early as 1 March and as late as 20 August. The ibises normally nest once per year, although it is possible that occasionally a second nesting may occur after an unsuccessful first attempt. The ibises at Shala nest in discrete groups; several nesting groups may form on any or all of the islands; the number of groups attempting to nest varied from year to year. Nesting activity begins when males arrive and establish pairing territories, usually in a small tree but sometimes on the ground. When females and other males arrive at the pairing territories, pair formation ensues. At this time males perform forward threat, modified forward threat, pursuit flight, supplanting attack and modified snap displays, while both sexes perform stretch and bow displays. Once established, the pair abandons the pairing territory and moves to the nesting area, usually near but always distinct from the pairing territory, and establishes a nest-site territory. Most members of the nesting group move to the nesting area on the same day. Copulation then takes place, and is followed by collection of nest material, usually by the male. Nests are built close together. The average area of 10 nests measured was 0.09 m². Nests are usually less than 20 cm thick and are made of many small branches and sticks. The average clutch in 34 nests was 2.24 eggs; the average size of 34 eggs was 63.4×43.5 mm. Incubation probably begins when the clutch is complete. Both sexes incubate, and the incubation period probably lasts 28–29 days. The development of the young is described. The young leave the nest-site territory when 14–21 days old. Although they are capable of some flight when 35–40 days old, the young do not leave the colony until they are 44–48 days old. In the colony, both parents care for the young. Usually only one parent at a time is with the young. The parents recognize their own young and are usually recognized by them. The behavioural interactions between young and parents are described. Fledging success in 1968 was 1.06 young per pair. The number of pairs successfully rearing young varied annually from none to 81%, on average over six years (1966–70, 1972) 35%. Predation at the breeding colonies is minimal. The food of one one-month old chick consisted of beetle larvae, lepidopteran larvae and beetles. Feeding areas, although undetermined, must be widespread. Inter-specific competition between Sacred Ibis and other nesting birds at Shala is discussed. Among possible factors stimulating nesting at Shala one, fairly heavy rainfall, seems to be especially important. It is also suggested that especially heavy rain-storms cause ibises to abandon the colonies, and result in poor breeding success.     

Nest sites as limiting resources for cavity‐nesting birds in mature forest ecosystems: a review of the evidence

ABSTRACT Assumptions that populations of cavity‐nesting birds are limited by access to nest sites have largely been based on anecdotal reports or correlative data. Nest‐box‐addition experiments or tree‐cavity‐blocking experiments are potentially rigorous ways to investigate how densities of breeding birds are affected by access to nest cavities. Experimental evidence indicates that natural tree holes are limited in human‐altered landscapes, but the possibility that cavity nests are limited in old growth (unmanaged) forests is less clear. I reviewed 31 nest‐cavity‐removal or addition experiments conducted with 20 species of cavity‐nesting birds in mature forests. Of these 31 experiments conducted with a variety of different species of birds, only 19% reported statistically significant changes in breeding densities. However, none of these studies included data about the reproductive history of individuals colonizing the boxes (i.e., whether birds using the boxes would have otherwise been floaters or that birds excluded from blocked cavities on the plots did not simply move elsewhere), so they provided no strong evidence that the number of breeding pairs was limited by availability of nest sites at the population scale. Although some studies indicate that nest sites are limited at local (plot) scales in old growth forests, there is still little empirical evidence for nest‐site limitation at the population‐ and landscape‐level in mature, unmanaged forests. I review the challenges in designing and interpreting box‐addition experiments and highlight the main gaps in knowledge that should be targeted in the future.     

BREEDING BIOLOGY OF THE BEARDED VULTURE IN SOUTHERN AFRICA,PART III: THE POST-NESTLING DEPENDENCE PERIOD

Brown, C. J. 1990. Breeding biology of the Bearded Vulture in southern Africa, Part III: The post-nestling dependence period. Ostrich 6l: 43–49.

The post-nestling dependence period of the Bearded Vulture Gypaetus barbatus in southern Africa begins with the first flight of the young bird at 126 ± 2 days after latching (November-January) and ends during the pre-laying nod or the parent birds' next breeding attempt (April-June), a nod of about five months. For the first two weeks after first flit young bid remaine6 within about 200m of the nest, moving up to 800 m by the third week. By a month out of the nest young birds spent about 40% of the day in flight, moved up to 3 km from the nest, began bone-dropping and interacting with young birds from neighbouring nests. At six weeks they began to accompany their parents for part of some of their foraging trips, but returned to the nest alone, and by eight weeks they completed foraging forays with parents Pasting up to 3 h. At 2–3 months out of the nest young birds covered an area of about 42 km², excluding the foraging trips with parents, by 3–4 months, 78km² and 4–6 months, 168 km². Parent birds delivered food for at least five months after the young bird's first flight. Young birds left their natal areas of their own accord, usually during the first month of their parents' next breeding attempt.     

Ontogeny of the daily profile of plasma melatonin in European starlings raised under long or short photoperiods

Photoperiodic manipulation of young European starlings suggests that their reproductive physiology is incapable of responding to a short photoperiod until they are fully grown. This study aimed to determine whether the lack of response to a short photoperiod is reflected in the daily profile of plasma melatonin concentrations. Five-day-old starlings taken from nest boxes showed a significant (p < 0.0001) rhythm in plasma melatonin concentrations, with high values during night. In nestlings hand-reared from 5 days of age on a long photoperiod (LD 16:8), equivalent to natural photoperiod at the time, the amplitude of the daily rhythm in melatonin increased significantly (p < 0.01) with age until birds were fully grown (20 days old). In nestlings reared on a short photoperiod (LD 8:16), the daily melatonin profile remained almost identical to that of long photoperiod birds until they were fully grown. However, after 20 days old, the duration of elevated nighttime melatonin began to extend to encompass the entire period of darkness. In contrast, fully grown starlings transferred from a long to a short photoperiod had partially adapted to the short photoperiod after 5 days; by 10 days, the daily melatonin profile was identical to that of birds held chronically on a short photoperiod. Thus, consistent with responses of reproductive physiology, the pineal of young birds appears to be incapable of perceiving, or adapting to, a short photoperiod.     

Seed Dispersal of a High Quality Fruit by Specialized Frugivores: High Quality Dispersal?1

Dispersal quality, as estimated by the cumulative effects of dispersal, germination, seed predation, and seedling survival, was examined for Beilschmiedia pendula (Lauraceae) in Monteverde, Costa Rica. I determined the pattern of dispersal by finding seeds deposited by birds, protected the seeds from seed predators with cages to assess germination and seedling survival, and examined seed predation rates with marked seeds. Seed predation, germination, and seedling survival were compared between seeds naturally dispersed by birds and seeds placed at randomly located sites. Approximately 70 percent of seeds dispersed by birds (N= 244) were deposited <10 m from crown edges of fruiting B. pendula trees, although some seeds were dispersed at least 70 m away. Larger seeds were more likely to be dispersed under or close to the parent trees, and larger seeds produced larger seedlings. Seed size was not correlated directly with seedling survival, but larger seedlings at three months were most likely to survive one year. Seed predation by mammals and insects and seedling mortality due to fungal pathogens were concentrated beneath the crowns of parent trees. Seedlings and saplings were more abundant beneath fruiting B. pendula trees, but individuals farther away were taller on average. Thus, dispersal is beneficial for B. pendula, but such benefits appear most pronounced at a small spatial scale; seeds dispersed >30 m from the crown edges actually had a lower probability of survival than those dispersed 10–20 m. Only 10 percent of B. pendula. seeds received high‐quality dispersal in terms of landing in the zone with the highest per seed probability of seedling survival 10–20 m from parental crowns.     

Behavior and Movement of Wild Turkey Broods

Behavioral and movement ecology of broods are among the most poorly understood aspects of wild turkey (Meleagris gallopavo) reproductive ecology. Recent declines in wild turkey productivity throughout the southeastern United States necessitate comprehensive evaluations of brood ecology across multiple spatial scales. We captured and marked 408 female wild turkeys with global positioning system (GPS)-transmitters across 9 pine (Pinus spp.)-dominated study sites in the southeastern United States during 2014–2019. We evaluated various aspects of the behavioral and movement ecology of 94 brood-rearing females until brood failure or 28 days after hatch (i.e., when poults are classified as juveniles). We found that 34 (36.2%) females had broods (≥1 poult) survive to 28 days after hatch. Broods moved >500 m away from nest sites the day after hatching, and then moved progressively farther away from nest sites over time. Daily movements increased markedly the first 3 days after hatching, and broods moved >1,000 m/day on average thereafter. Females roosted broods an average of 202 m away from nest sites the first night after hatching, but distances between consecutive ground or tree roosts were variable thereafter. Daily core areas increased from 0.8 ha the day of hatch to 4.6 ha by day 28, and range sizes increased from 6.9 ha to 27.9 ha by day 28. Broods tended to consistently select open land cover types, whereas selection for other land cover types varied temporally after hatch day. Broods spent 89% of their time foraging. Predicted daily survival for broods decreased rapidly with increasing distance moved during the initial 3 days after hatching and showed less variation during the subsequent 2 weeks post-hatch. Our findings parallel previous researchers noting that the most critical period for brood survival is the first week after hatch day. Previous researchers have attempted to identify vegetative communities used by broods under the assumption that these communities are a primary factor influencing brood success; however, our results suggest that brood survival is influenced by behavioral decisions related to movements during early brooding periods. © 2020 The Wildlife Society.     

Mortality of Wood Warbler Phylloscopus sibilatrix nests in Welsh Oakwoods: predation rates and the identification of nest predators using miniature nest cameras

Capsule Predation was the main cause of nest failure, but predation rates have remained unchanged since the 1980s. Eurasian Jays Garrullus glandarius were the most common predator.

Aims To quantify, and compare, nest predation rates for 1982–84 and 2009–11, and to identify predators of Wood Warbler Phylloscopus sibilatrix nests in Welsh oakwoods.

Methods During 2009–11, 167 Wood Warbler nests were monitored and purpose-built miniature nest cameras deployed at 73 of them. Nest predation rates were compared with 67 nests monitored during 1982–84.

Results Of 167 nests monitored from 2009 to 2011, 62 failed due to predation (32/73 camera nests, 30/94 non-camera nests), giving an overall Daily Survival Rate (DSR?±?se) of 0.979?±?0.003. This was not significantly different from the rate during 1982–84 (0.967?±?0.006). In 2009–11, the DSR of nests declined temporally during the season at both the egg and chick stages. For chick stage nests, DSR varied annually and nonlinearly with age of nestlings. There was no evidence for an effect of cameras at either stage. Of 32 camera nests lost to predation, the predator was identified from 28, resulting in 30 predators being identified. There was one case of multiple predators at a single nest. The majority of nest predation was carried out by birds (28/30), predominantly Eurasian Jays (18/28), but also Common Buzzards Buteo buteo (5/28), Great Spotted Woodpeckers Dendrocopos major (3/28) and Eurasian Sparrowhawks Accipiter nisus (2/28). There was one predation by both a Eurasian Badger Meles meles and a Red Fox Vulpes vulpes. There were no records of Grey Squirrels Sciurus carolinensis depredating nests.

Conclusions Nest predation rates were similar in both periods, suggesting that increased rates of nest predation have not been driving the decline of the Wood Warbler population in Wales. Deployment of nest cameras did not affect nest survival rates and were successful in identifying nest predators, the majority of which were avian, especially Eurasian Jays. Knowledge of the identity of nest predators can aid the development of conservation measures.     

Nest‐dwelling ectoparasites influence the start and duration of the first pre‐basic moult in the European starling Sturnus vulgaris

Nest‐dwelling ectoparasites represent an early stressor for birds as they impair the development of nestlings, which can adaptively respond by adjusting their growth rate to current conditions. While nest ectoparasites have long‐term effects on nesting adults, no study has examined if they also have an impact on the moult patterns of juveniles. Herein, we investigated whether the presence of ectoparasites in the nest influences the start and duration of the first pre‐basic moult in the European starling. To do so, we experimentally removed nest‐dwelling ectoparasites from a group of nests and used another group of unmanipulated (i.e. naturally infested) nests as the control. The moult began at an earlier age and lasted longer in birds from the ectoparasite‐free nests compared to their control counterparts. The timing of the moult was also affected by the hatching date (i.e. birds that fledged later had shorter moults) and the brood size (i.e. birds in larger broods started their moult at an older age). We also found evidence that the removal of nest ectoparasites influenced the condition of individuals during the course of the moult. In the control birds, we observed a decrease in hematocrit levels, but these were unaltered in the birds fledged from the ectoparasite‐free nests. Our study shows that nest‐dwelling ectoparasites adversely affected the timing of the moult and the individual condition of juvenile starlings, with possible major consequences for their subsequent life‐history events.     

The breeding biology of the Scimitarbilled Woodhoopoe

Steyn, P. 1999. The breeding biology of the Scimitarbilled Woodhoopoe. Ostrich 70 (3&4): 173–178.

The breeding biology of the Scimitarbilled Woodhoopoe Rhinopomastus cyanomelas was studied at two sites in Zimbabwe over a 13-year period from 1964–1977. The pairs were resident, remained together throughout the year, and inspected their nest sites occasionally during the non-breeding season. The breeding season extended from August to December with a marked September/October peak. Eggs were laid at daily intervals. Clutch size averaged 2.9 (range 2–4). Incubation began either with the penultimate or last laid egg. During the 13–14 day incubation period the female left the nest only occasionally each day and was reliant on the male for food. This pattern continued for four days after the chicks hatch. Thereafter she started to forage and gradually increased her contribution to chick provisioning until she overtook that of the male. With one exception, he never fed the chicks directly and delivered the food to the female. The nestlings were brooded overnight for the first two weeks. The anti-predator response of the young included a malodorous brown exudation from the preen gland and unpleasant liquid excreta. The nestling period was 21–24 days and the young left the vicinity of the nest with their parents and did not return to roost in it. Twelve breeding cycles were monitored and 76% of eggs laid (n=37) produced fledged young. Second broods were raised in the same nest on two occasions after successful rearing of the first, presumably by the same pair, but the birds were not individually marked. There was no evidence of helpers at the nest.     

LETTERS

We used video recordings to perform a behavioural analysis of a Village Weaver Ploceus cucullatus colony in Awash National Park, Ethiopia. We focused specifically on female behaviour during the pair-formation, egg-laying and early-incubation phases of the nesting cycle. A factor analysis revealed that females’ temporal investments can be partitioned into three broad behavioural categories: (1) behaviours associated with aggression, (2) time away/ inside nest, and (3) behaviours associated with copulation. Time budgets revealed females spent approximately 61% of their time away from the colony and 38% of their time inside their nests. The performance of individual behaviours was largely a function of temporal and social factors, including when the birds were observed and the personality of the territorial male. Females invested more time away from the nest earlier and more time inside the nest later in the observation period. One aspect of a territorial male’s personality, boldness, was a predictor of several female behaviours: a female Village Weaver was significantly more likely to remain on a territory if the resident male had a tendency not to flee during colony-wide disturbances. Lastly, a path analysis revealed that females exhibited consistent sequential patterns of behaviour.     

Overnight foraging trips by chick‐rearing Nazca Boobies Sula granti and the risk of attack by predatory fish

Most tropical booby species complete breeding foraging trips within daylight hours, thus avoiding nights at sea. Nazca Boobies Sula granti are unusual in this respect, frequently spending one or more nights away from the nest. We used GPS dataloggers, time‐depth recorders, and changes in body weight to characterize foraging trips and to evaluate potential influences on the decisions of 64 adult Nazca Boobies to spend a night at sea, or to return to their chicks on Isla Española, Galápagos, in daylight hours. The tagged birds foraged east of Isla Española, undertaking both single‐day (2–15 h, 67% of trips) and overnight trips (28 h–7.2 days, 33%), and executing 1–19 foraging plunge‐dives per single‐day trip. Birds might forage longer if they are in nutritional stress when they depart, but body weight at departure was not correlated with trip length. Birds might be expected to return from longer trips with more prey for young, but they returned from single‐day and overnight trips with similar body weights, consistent with previous indications that Nazca Boobies forage until accumulating a target value of prey weight. Birds with a lower dive frequency during the first 5 h of a trip were more likely to spend the night at sea, suggesting that they might choose to spend the night at sea if prey capture success was low. At night, birds almost never dived and spent most of their time resting on the water’s surface (11.8–12.1 h, > 99% of the time between civil sunset and civil dawn). Thus, the night is an unproductive time spent among subsurface predators under low illumination. The birds’ webbed feet provided evidence of this risk: 24% of birds were missing > 25% of their foot tissue, probably due to attacks by predatory fish, and the amount of foot tissue lost increased with age, consistent with a cumulative risk across the lifespan. In contrast, other tropical boobies (Blue‐footed Sula nebouxii and Brown Boobies Sula leucogaster), which do not spend the night on the water, showed no such damage. These results suggest that chick‐rearing Nazca Boobies accept nocturnal predation risk on occasions of low prey encounter during a foraging trip’s first day.