Use of surrogate parental models and age periods in a successful release of hand-reared sandhill cranes

Ten sandhill crane chicks were reared in isolation from humans to prepare them for an experimental wild release. They were imprinted on realistic models using crane brooding calls and were fed by crane-like puppets. Six of the chicks were simultaneously imprinted on a human in a crane costume. The other four chicks were introduced to this surrogate parent at 5–7 days of age. The chicks were fed natural foods by the parent at two wild sites, one of which, the release site, was a staging area for migratory cranes. Observations were made on their behavioral development, including the time spent close to the model or costumed parent and the percentage of time spent foraging. The chicks spent the initial month close to the surrogate parent but moved away more to forage during the second month. The chicks regressed to again spend a great deal of time near the parent during the third and fourth months. They were released during this regressive period by removing the surrogate parent. All five of the released chicks showed increased interest in wild cranes within days of the release and formed a continuous association with wild cranes within 30 days. Four of the five were relocated by telemetry the following spring back in Wisconsin. These young juvenile cranes were excellent candidates for release due to their adaptable nature and their level of social development. The artificial stimuli of the surrogate parent helped the chicks to generalize their attachment to wild cranes. Once with wild cranes they quickly learned additional survival skills.     

Vocalizations of chicks and juveniles and the development of adult calls in the Aldabra White-throated rail Dryolimnas cuvieri aldabranus (Aves: Rallidae)

Calls were recorded from eggs, chicks and juveniles of the Aldabra White-throated rail Dryolimnas cuvieri aldabranus. A sonagraphic analysis was made of these calls, their behavioural contexts described and probable functions suggested. Three calls, the twitter, tiuu and contented peep were produced by chicks in the egg. All three calls may be derived from the basic peep first recorded some 36 hours before hatching. Shortly after hatching two more calls, the distress call and the alarm call, can be elicited from the rail chicks. Contented peeps and twitters are restricted to the repertoire of young rails. Song was first heard from wild rail chicks at the age of ten days and may develop from the contented peep. Three adult calls, the 'mp yeah, 'mptiuu and 'mpclick appear at the age of three months and six months later the adult vocal repertoire is completed by the appearance of 'mps, toks, purrs and nest-defence squeals. With the exception of the 'mp, all adult calls can be derived from the vocalizations of chicks and juveniles.     

Hand-rearing,growth, and development of the red bird of paradise (Paradisaea rubra) at the New York Zoological Park

Growth and development of six hand-reared red bird of paradise chicks was documented at the New York Zoological Park from March 1988 to May 1989. A total of 16 eggs were laid, of which 10 were fertile. Clutches consisted of two eggs and the female left the next infrequently during incubation. Two chicks left in the nest were apparently victims of parental abuse. Eggs were subsequently removed from the nest after 10–14 days, candled, and if fertile, were artificially incubated. The average incubation period was 16.6 days. Newly hatched chicks were without down and their eyes remained closed until approximately 6 days of age. Hand-reared chicks were maintained in Air Shield Infant Isolettes. The weight of newly hatched chicks was about 8 g, and the weight typically doubled during the first week. Ratios of food intake to body weight were highest between day 4 and 10. Pin feathers were visible on the wings after 4 days, and after 3 weeks, the chicks were fully feathered. Analysis of the diet revealed acceptable levels of iron, but vitamin A and E levels were higher than recommended for poultry chicks. This paper documents the first successful hand-rearing of any species of birds of paradise from hatching to fledging.     

Growth and development of infant giant pandas (Ailuropoda melanoleuca) at the Wolong Reserve,China

From 1991 to 1993 inclusive, seven infant giant pandas (Ailuropoda melanoleuca) were born at the China Conservation and Research Center for the Giant Panda. Average daily weight gain in the first 6 months for mother-reared infants (n = 5) was 71.3 g/day; for one partially mother-reared and partially hand-reared infant, 41.5 g/day; and for one completely hand-reared infant, 50.3 g/day. There was a significant difference in growth rates across the first 6 months in all methods of rearing. In addition, a comparison of growth rates across the three rearing methods showed significant differences in the first, second, third, fifth, and sixth months. Average daily body length increase for mother-reared infants was 4.1 mm/day; for partially mother-reared/partially hand-reared infants, 4.0 mm/day; and for the completely hand-reared infant, 2.8 mm/day. In mother-reared infants, body length increase during the first month was significantly greater than during the following months, and was slowest during the sixth month. At birth, infants were all pink in color with a light white coat of lanugo. Black pigmentation was first noted at 7–10 days of age, which was also the time that initial hair coat growth was seen. Eyes opened at 35–48 days of age. Ears opened at 31–50 days of age. Deciduous dentition was first seen at 82–121 days of age, while permanent dentition began to erupt at 350 days of age. © 1996 Wiley-Liss, Inc.     

Aufzucht von Chilemeerespelikane (Pelecanus occidentalis thagus) im Vogelpark Walsrode mit Vergleichen zu anderen publizierten Erfahrungen mit Pelikanen

The probable world first captive breeding success in Chilean Brown Pelican (Pelecanus occidentalis thagus) in captivity is reported. Two chicks were hand reared at Walsrode Birdpark, Germany in 2006. Parents were imported in October 2005 and were wild birds that had been injured and subsequently rescued. All 10 adult birds demonstrated detrimental and chronically handicaps. First eggs were laid in January 2006. Eggs were incubated artificially at 37.1 °C and 56% rel. humididty. Two chicks hatched after 33 days of incubation. First feeding was made one day after hatching in the morning. Food was given 5 times a day. Until the 8th day after hatching, exclusively cut naked baby rats were fed. For stimulating the digestion and providing a good intestinal flora Lactobacillus powder was used and food was warmed up before application. After 8 days the diet was changed to fish. For development see figures. Worth to mention is the black-purple colour of the freshly hatched chicks which became successively paler with age. Also the development of the feather areas is characteristic for this (sub)-species. Taxonomy is discussed with some morphological arguments that are typical for subspecies. Nevertheless, some indications of possible breeding barriers between subspecies could support the suggestions for species status. Hatching and rearing data are compared with dates from other zoos and species of pelicans. The good development of the Walsrode birds based on the data and methods described leaves this article useful as a reference guideline for hand rearing pelicans.     

Aufzucht von Chilemeerespelikane (Pelecanus occidentalis thagus) im Vogelpark Walsrode mit Vergleichen zu anderen publizierten Erfahrungen mit Pelikanen

The probable world first captive breeding success in Chilean Brown Pelican (Pelecanus occidentalis thagus) in captivity is reported. Two chicks were hand reared at Walsrode Birdpark, Germany in 2006. Parents were imported in October 2005 and were wild birds that had been injured and subsequently rescued. All 10 adult birds demonstrated detrimental and chronically handicaps. First eggs were laid in January 2006. Eggs were incubated artificially at 37.1 °C and 56% rel. humididty. Two chicks hatched after 33 days of incubation. First feeding was made one day after hatching in the morning. Food was given 5 times a day. Until the 8th day after hatching, exclusively cut naked baby rats were fed. For stimulating the digestion and providing a good intestinal flora Lactobacillus powder was used and food was warmed up before application. After 8 days the diet was changed to fish. For development see figures. Worth to mention is the black-purple colour of the freshly hatched chicks which became successively paler with age. Also the development of the feather areas is characteristic for this (sub)-species. Taxonomy is discussed with some morphological arguments that are typical for subspecies. Nevertheless, some indications of possible breeding barriers between subspecies could support the suggestions for species status. Hatching and rearing data are compared with dates from other zoos and species of pelicans. The good development of the Walsrode birds based on the data and methods described leaves this article useful as a reference guideline for hand rearing pelicans.     

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.     

Captive breeding for reintroduction: influence of management practices and biological factors on survival of captive kaki (black stilt)

An important component of the restoration strategy for the critically endangered kaki or black stilt (Himantopus novaezelandiae) is captive breeding for release. Since 1981 1,879 eggs were collected from wild and captive pairs, with birds laying up to four clutches. Eggs were incubated artificially and most chicks reared by hand until released as juveniles (about 60 days) or sub‐adults (9–10 months). Because survival in captivity is a significant determinant of the number of birds available for release, we wished to identify sources of variation in mortality to assess potential impacts of management on productivity. Hatchability was 78% for captive‐laid eggs and 91% for wild‐laid eggs. Survival of hatched eggs was 82% by 10 months of age for both wild and captive birds. Most egg mortality occurred early in incubation and around hatching: the timing of mortality was unaffected by whether birds were captive or wild, hybrid or pure kaki, or when eggs were laid. Heavier hatchlings showed higher initial survival, as did chicks from wild parents. Hatchlings from fourth‐laid eggs showed lowest survival, even though hatchling mass tended to increase with hatch order. Survival of chicks subjected to major health interventions was 69% after 4 months. No differences in survival were found between different genders, hybrids and pure kaki, hand‐reared or parent‐reared birds, chicks hatching early or late in the season, different seasons, different‐sized groups of chicks, chicks reared in different brooders, juveniles kept in different aviaries, and chicks from subsequent clutches. Birds subjected to minor health interventions were equally likely to survive as healthy chicks (82%). Survival was high despite aggressive management (quadruple clutching and collecting late in the season). Differences between captive and wild birds suggest further improvements could be made to captive diet. Wide variation in hatchability between parent pairs substantiates the practice of breaking up poorly performing pairs. Zoo Biol 0:1–16, 2005. © 2005 Wiley‐Liss, Inc.     

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.     

Breeding condors in captivity for release into the wild

Recognizing the decline of the South American Condor in some parts of its range and the highly endangered status of the California condor, the New York Zoological Society developed a captive-breeding program for South American condors. This program was designed to produce techniques applicable to hand-rearing of either species of condor. Once condors were successfully reared in captivity, it became imperative to develop techniques to ensure that captive-reared condor chicks could be released into the wild, could survive there, and could interact naturally with other wild condors. Captive-bred hand-reared condor chicks were taken to Northwestern Peru and successfully released into the wild.     

Notes on the behavioural ecology of the Magnificent Frigatebird Fregata magnificens

The Magnificent Frigatebird population breeding on Man-o-War Cay, Belize in 1980 laid their single eggs between mid-December and early April, and had a mean hatching date of mid- to late April. There were no differences between the sexes in the percent of time spent incubating eggs or brooding small chicks (males 48%, females 52%). However, males were not observed to feed larger (75–100 d) chicks. All 81 feedings of juvenile (approximately 1 year old) frigatebirds observed during 126 hr of observations were by females, and the majority of these feedings occurred at midday (46%) when approximately equal numbers of females and juveniles frequented the study area. Our data confirm Diamond's (1972, 1973) reports of unequal roles in chick rearing and post-fledging care between male and female F. magnificens , and support the hypothesis that males and successful females may breed at one- and two-year intervals, respectively.     

Taming parent‐reared orange‐winged Amazon parrots by neonatal handling

Tameness in parrots is often achieved by artificial rearing, in which chicks are typically removed from parents, fed a liquified or semi‐liquified diet by oral gavage and maintained in thermally controlled brooders until they are grown. As an alternate means of rearing birds, we tested whether occasional neonatal human handling of parent‐reared chicks might produce tameness while reducing the risk of sexual imprinting on humans. Orange‐winged Amazon chicks (Amazona amazonica) were incubated and hatched by wild‐caught parents, then were temporarily removed from the nest box, and handled at various times during the nestling period. In Trial 1, handled chicks (n = 6) were handled from days 10 to 39 of age for 10–20 min/day and from 40 days to fledging (days 56–/57) for 20–30 min/day. Nonhandled chicks (n = 4) were handled only to record body weight and provide medication, as needed. After fledging, chicks were evaluated for tameness, e.g., by their willingness to approach the handler, perch on a finger, be touched on the head, and by their respiratory rate in the presence of the handler. Handled birds differed significantly in all indices of tameness. In Trial 2, handled chicks were handled for 30 min, four times/week either from days 15 to 36 (n = 3) or 35 to 56 (n = 3); results were similar to Trial 1. Chicks handled later tended to be slightly tamer than those handled earlier. In both trials, the amount of time that handled chicks were in contact with humans was less than 2% of the time they spent with conspecifics. It is therefore unlikely that these chicks imprinted either filially or sexually on humans, although this has not been experimentally tested. While continued handling is likely necessary to maintain tameness, these results support the concept that neonatal handling of parent‐raised parrots provides a low‐labor and low‐technology alternative to artificial rearing as a means of initially taming birds, thereby improving their adaptation to life in captivity. Zoo Biol 18:177–187, 1999. © 1999 Wiley‐Liss, Inc.     

Establishment Success of Experimentally Delayed Juvenile Marsh Tits Parus palustris

By experimentally manipulating the time when young marsh tits, Parus palustris, could become established, I tested the influence of size, hatching date, social dominance in caged situations, and time of season on establishment success. Individuals that managed to become established were divided into two groups: those that became established in new territories and those that were found in the same territory as the one where they were caught. In no circumstances did size, hatching date or social dominance influence establishment success. The only factor tested that had a significant effect on establishment success, was when the juveniles were released; those that established themselves in new territories had been released earlier than unsuccessful ones. Thus, prior occupancy rather than hatching date per se is the factor determining establishment in new territories. Juveniles that became re-established in their former territory had been released significantly later than those not becoming re-established. As the season progresses, increasingly fewer unestablished juveniles are present to fill vacancies. Thus, late-released juveniles stood a better chance of finding their flock position still vacant compared with juveniles released early, whose previous positions would already have been occupied by other juveniles.     

Development of spatial memory in occlusion-experienced domestic chicks

At around day 11 of life, domestic chicks show a tendency to move out of sight of their mother before returning and regaining social and visual contact. We conducted a series of experiments to investigate the role of this voluntary ‘out-of-sight’ behaviour on the development of spatial memory in young chicks. We compared the behaviour of chicks that were reared in environments that provided opportunities to move out of sight of an imprinting stimulus (occlusion-experienced chicks) with the behaviour of chicks that were given minimal occlusion experience (controls). As in natural conditions, out-of-sight behaviour peaked on day 11. When chicks were released into larger pens at 14 days of age, occlusion-experienced chicks walked more than control chicks, but otherwise showed similar degrees of dispersal. Occlusion-experienced chicks tended to show better (although not significant, P=0.09) retrieval of a visually displaced imprinting stimulus than control chicks. Time spent out of sight in the rearing pens was negatively related to the number of orientation errors in a detour test. Occlusion-experienced chicks also tended to make fewer orientation errors in the first trial (P=0.07) and in subsequent trials (P=0.05). In contrast, experimentally manipulating the amount of time that chicks were out of sight of an imprinting stimulus (by confining the chicks) had no effect on their performance in displacement or detour tests. The results presented here suggest that active experience of occlusion around day 11 improved egocentric orientation towards an out-of-sight goal, supporting the hypothesis that enrichment-induced behavioural changes are dependent on the interaction with objects.     

Ontogenetic Behavior and Migration of Gulf of Mexico Sturgeon, Acipenser oxyrinchus desotoi, with Notes on Body Color and Development

We observed Suwannee River Gulf sturgeon, Acipenser oxyrinchus desotoi, in the laboratory and found free embryos (first interval after hatching) hid under rocks and did not migrate. Thus, wild embryos should be at the spawning area. Larvae (first interval feeding exogenously) initiated a slow downstream migration, and some juveniles (interval with adult features) continued to migrate slowly for at least 5 months, e.g., a 1-step long larva-juvenile migration. No other population of sturgeon yet studied has this migration style. A conceptual model using this result suggests wild year-0 sturgeon have a variable downstream migration style with short-duration (short distance) migrants and long-duration (long distance) migrants. This migration style should widely disperse wild fish. The model is supported by field studies that found year-0 juveniles are widely dispersed in fresh water to river km 10. Thus, laboratory and field data agree that the entire freshwater reach of river downstream of spawning is nursery habitat. Foraging position of larvae and early juveniles was mostly on the bottom, but fish also spent hours holding position in the water column, an unusual feeding location for sturgeons. The holding position of fish above the bottom suggests benthic forage in the river is scarce and fish have evolved drift feeding. The unusual migration and foraging styles may be adaptations to rear in a river at the southern limit of the species range with poor rearing habitat (low abundance of benthic forage and high summer water temperatures). Suwannee River Gulf sturgeon and Hudson River Atlantic sturgeon, A. o. oxyrinchus, are similar for initiation of migration, early habitat preference, and diel migration. The two subspecies differ greatly for migration and foraging styles, which is likely related to major differences in the quality of rearing habitat. The differences between Atlantic sturgeon populations show the need for geographical studies to represent the behavior of an entire species.     

Are antipredator behaviours of hatchery Salmo salar juveniles similar to wild juveniles?

This study explores how antipredator behaviour of juvenile Atlantic salmon Salmo salar developed during conventional hatchery rearing of eggs from wild brood stock, compared with the behaviour of wild‐caught juveniles from the same population. Juveniles aged 1+ years were tested in two unfamiliar environments; in one S. salar were presented with simulated predator attacks and in the other they were given the opportunity to explore an open‐field arena. No difference was found in their spontaneous escape responses or ventilation rate (reflex responses) after simulated predator attacks. Hatchery‐reared juveniles were more risk‐prone in their behaviours than wild‐caught individuals. Hatchery juveniles stayed less time in association with shelter. In the open‐field arena, hatchery juveniles were more active than wild juveniles. Hatchery juveniles were also immobile for less time and spent a shorter amount of time than wild juveniles in the fringe of the open‐field arena. Salmo salar size had no effect on the observed behaviour. Overall, this study provides empirical evidence that one generation of hatchery rearing does not change reflex responses associated with threats, whereas antipredator behaviour, typically associated with prior experience, was less developed in hatchery‐reared than in wild individuals.     

Effects of begging on growth rates of nestling chicks

We investigated whether an increase in begging levels delaysgrowth of chicks. In experiment 1, we hand-reared nine pairsof ring dove squabs, divided into a control and a begging group.All squabs received similar amounts of food, but those in thebegging group had to beg for a prolonged period in order tobe fed, while squabs in the control group received food withoutbegging. Squabs stopped responding to the treatment after 10days and, at that time, there was no effect of induced beggingon their body mass. In experiment 2, we hand-reared 27 pairsof magpie chicks for 3 days. The design of experiment 2 wassimilar to that of experiment 1. Daily food intake and beggingaffected growth rates. On average, chicks in the begging groupgrew 0.8 g/day less than control chicks, which represents adecrease of 8.15% in growth rate. Because growth is usuallypositively associated with expected fitness, this demonstratesthat begging is a costly behavior, an assumption routinelymade in models of begging behavior.     

Incubation and hatch management: consequences for bone mineralization in Cobb 500 meat chickens

From ~35 days of age fast growing meat chickens spend extended periods sitting or lying and less time standing. In a fast-feathering parent line lower early incubation temperatures which delayed chick hatch time, improved bone ash and extended their standing time. This incubation study assessed the consequences of incubation temperatures, hatch time and chick management at hatch/take off on femoral bone ash (BA) in Cobb 500 meat chickens. Embryos were incubated under either Control (between 37.8°C and 38.2°C egg shell temperature (EST)) or a Slow start (from 37.2°C at sett (the start of incubation), reaching 37.8°C EST at day 13 incubation), temperatures. Hatched chicks were identified at 492 h (20.5 days of incubation – classified as early (E)) or, between >492 and ⩽516 h (>20.5 and ⩽21.5 days of incubation – classified as late (L)), from setting. The E hatch chicks were allocated across three post-hatch treatments; treatment 1: E hatch chicks that were sampled E at 492 h from setting; treatment 2: E hatch chicks that were fed for a further 24 h in a floorpen before being sampled L at 516 h from setting; treatment 3: E hatch chicks that spent a further 24 h in the incubator before being sampled L at 516 h from setting. All L hatch chicks formed one treatment group which was sampled L at 516 h (i.e. L hatch chicks sampled L). It is not possible to sample L hatching chicks E hence this treatment is absent from the experimental design. Slow start incubation resulted in a higher total hatch percentage with a greater proportion of chicks hatching L, compared with the Control incubation. The L hatching chicks had significantly higher BA than the E hatching chicks. Of the E hatching chicks, those sampled both E and L had significantly lower BA than E hatching chicks fed for 24 h before L sampling. The E hatch, fed and sampled L chicks had the numerically highest BA, which was not significantly different from the BA of the L hatching chicks sampled L These results demonstrate that BA at hatch can be improved, either by extending the incubation period through a Slow start incubation profile, inducing L hatch, or alternatively, via the prompt provision of feed to E hatching chicks.     

Assessing the influence of the entomopathogenic nematode Heterorhabditis baujardi LPP7 (Rhabiditina) on embryogenesis and hatching of the plant-parasitic nematode Meloidogyne mayaguensis (Tylenchina)

Two assays were conducted to assess the influence of infective juveniles (IJs) of Heterorhabditis baujardi LPP7 on the embryogenesis and hatching of Meloidogyne mayaguensis. In the first assay, eggs were incubated in water alone or in the presence of infective juveniles, and completion of embryogenesis was evaluated 14 days later. In the second assay, unhatched second-stage juveniles were incubated in distilled water alone or in the presence of infective juveniles. Cumulative hatching was compared at various time intervals. Embryogenesis was not affected, whereas second-stage juveniles hatching was delayed probably because of the eggs permeability to noxious metabolites released by Photorhabdus luminescens, which is the bacterial symbiont of H. baujardi.     

BREEDING BIOLOGY OF THE MANX SHEARWATER PUFFINUS PUFFINUS

Studies on the breeding biology of Puffinus puffinus were carried out in 1963 and 1964 at the large colony on Skokholm, Wales. During the six weeks before laying the birds spent up to a quarter of the days in the burrows, but the ten days immediately prior to laying were normally spent at sea. There is a prolonged laying period, with a marked peak in the first half of May. Details are given of a second egg being laid when the first was deserted immediately after being laid. The male took the first incubation spell. The incubation spells ranged from one to 26 days and averaged six. The incubation period was about 51 days. The frequency of visits to land by breeding birds, unlike those by non-breeders, was not affected by the moon. On hatching, the chicks grew rapidly and reached maximum weights of between 505 and 755 gm. sometime between 39 and 61 days. There was a variable desertion period, usually eight or nine days, before the chicks left the island about 70 days after hatching. During the feeding period the chick received about two feeds every three days. There is evidence that adults visited the chicks more frequently than this. There was no correlation between growth of the chicks, their feeding rates or fledging weights and the time of laying. There was a high survival (about 95 %) of chicks during the fledging period but some eggs were lost in disputes for burrows. Nine pairs in 1964 were unable to raise two young simultaneously. Parents altered their feeding rhythms to try to feed two young but did not themselves lose weight. It is suggested that the critical factor in the production of young is the availability of food for the young immediately after they leave the colonies.