Reproductive measures and chick provisioning of Cory's Shearwater Calonectris diomedea borealis in the Azores

Capsule Timing of breeding influenced wing-length at fledging, and egg size may be an indicator of fledging weight and the amount of food received by chicks.

Aims To investigate chick growth, temporal patterns of chick food provisioning and the importance of indices of parental condition or quality, egg size and hatching date, to predict nestling body mass and wing-length at fledging, and compare breeding and chick feeding characteristics between colonies in the northeast Atlantic.

Methods A survey of Cory's Shearwater nests was carried out at Vila islet. A sample of 52 chicks, ringed and weighed at hatching, was selected to study chick growth and food provisioning.

Results Hatching success (51%) was much lower than fledging success (87%). Both hatching date and egg size contributed to explain wing-length at fledging, but hatching date, which was negatively correlated with wing-length at fledging, had the most important contribution (22%). There was some indication that egg size may explain variation in fledging weight and the amount of food received by chicks. Food delivery and feeding frequency of chicks varied throughout the chick development stage and three phases were distinguished: (1) 0–29 days, the highest feeding frequency values and a linear increase in food delivery; (2) 30–69 days, an oscillation in food delivery and medium feeding frequencies; (3) 70–90+ days, a sharp decrease in both food delivery and feeding frequency.

Conclusion Variation in food availability did not seem sufficient to override the overall importance of indices of parental quality in determining reproductive measures and chick provisioning. Breeding and feeding characteristics were similar between colonies in the northeast Atlantic, with variability in chick provisioning higher further south.     

Larval sensory abilities and mechanisms of habitat selection of a coral reef fish during settlement

In most animals, siblings from a given reproductive event emerge over a very short period of time. In contrast, many species of birds hatch their young asynchronously over a period of days or weeks, handicapping last-hatched chicks with an age and size disadvantage. Numerous studies have examined the adaptive significance of this atypical hatching pattern, but few have attempted to explain the considerable intrapopulation variation that exists in hatching asynchrony. I explored proximate determinants of hatching asynchrony by monitoring 112 Burrowing Owl (Athene cunicularia) nests in the grasslands of southern Saskatchewan, Canada, over 4 years. Age disparities between first- and last-hatched siblings (i.e., hatching spans) varied considerably, ranging between 1 and 7 days (mode = 4 days). These hatching spans increased with increased hatching success. Hatching spans also increased with larger clutches, but the increase was less than predicted given the increased time required to lay more eggs. Hatching span was unrelated to number of prey cached in the nest during egg laying (an index of food availability), and was unaltered by a year of super-abundant prey. Furthermore, pairs given extra food during laying had hatching spans equal to those of unsupplemented control pairs. These results were inconsistent with both the energy constraint and facultative manipulation hypotheses, which predict that hatching asynchrony should vary with the level of food during laying, when incubation onset is determined. Burrowing Owls were apparently free of food limitation early in breeding, yet may not have been able to optimize hatching spans because food conditions during laying were largely unrelated to food conditions during brooding. Thus, one of the premises for facultative manipulation of hatching asynchrony—that laying females are able to forecast post-hatch food conditions—may not have been met for this population of Burrowing Owls.     

Maternal investment during egg laying and offspring sex: an experimental study of zebra finches

To study whether offspring sex is related to the amount of resources invested in eggs we performed an experiment on zebra finches, Taeniopygia guttata. By manipulating their food supply, we forced two groups of females either to increase or to decrease investment in subsequent eggs. Since zebra finches are sexually dimorphic and the reproductive value of the sexes may vary with maternal nutritional status, we predicted that females would adjust the sex of their offspring to egg quality. Females that received poor-quality food for 7 weeks before egg laying, then food supplemented with proteins after they laid the first egg, significantly increased the mass of subsequent eggs. An increase of egg mass with laying sequence was less pronounced in females that received high-quality food before laying and experienced food deterioration after starting to lay. The proportion of sons in subsequent eggs tended to increase in the latter group (although this was marginally significant) but was not related to laying sequence in the other group: these patterns differed significantly between the groups. Offspring sex was not related to egg mass, but newly hatched male chicks were heavier than female chicks. Furthermore, the hatching success of male eggs was lower than that of female eggs. We suggest that differential hatching success of the sexes and sex differences in mass at hatching may constitute important factors shaping brood sex ratios. Copyright 2002 The Association for the Study of Animal Behaviour. Published by Elsevier Science Ltd. All rights reserved.     

Breeding systems of New Zealand Snipe Coenocorypha aucklandica and Chatham Island Snipe C. pusilla; are they food limited?

New Zealand Snipe Coenocorypha aucklandica were studied over six breeding seasons on the Snares Islands. The study area (7.5 ha) held about 20 pairs at a density of 3.2 ± O.5 pairs/ha, plus 5 to 25 nonterritorial birds. Most matings were monogamous but simultaneous polygyny was recorded in one territory (by two different males) in four consecutive seasons. Males courtship fed females before egg-laying. The typical clutch was two eggs, laid three days apart. Incubation was shared equally by the sexes in monogamous pairs and took 22 days. Some females with polygynous mates attempted to incubate unaided, which took about 38 days. Broods were split at hatching, with the male caring for the first chick to leave the nest. Chicks were fed by adults for at least 41 days, and did not become independent until about 65 days old. Growth rates were slow compared to Common Snipe Gallinago gallinago and full plumage took about 54 days to attain. No pairs were double-brooded but 43% of pairs that failed during incubation or early chick-rearing renested together. Some breeders of both sexes who had lost their dependent chick bred a second time with a new mate while their first mate continued rearing the surviving chick (sequential polygyny and polyandry). Hatching success was 80%, and fledging success was 48%. Each pair produced, on average, O.6 fledglings per year. Chatham Island Snipe C. pusilla were studied on Rangatira Island during the 1983–84 breeding season. Breeding density was about 5.6 pairs/ha. The breeding system was very similar to that for C. aucklandica but chicks became independent at about 41 days old. Hatching success was 89%. Compared to Common Snipe, Coenocorypha snipes occurred at high densities, had courtship feeding, large eggs, a long interegy interval, a small clutch, shared incubation and a long incubation period. Nest desertion rates were high, but overall hatching success was also high, chick growth rates were slow, there was a long period of chick dependence and a long relaying interval following nest failure or chick loss. Survival rates of both adults and chicks were high. These differences are attributed to the absence of predation, and to intense intraspecific competition for food in a stable environment.     

Effects of intraclutch variation in egg size and hatching asynchrony on nestling development and survival in semi‐precocial Herring Gulls

Intraclutch egg size variation may non‐adaptively result from nutritional/energetic constraints acting on laying females or may reflect adaptive differential investment in offspring in relation to laying/hatching order. This variation may contribute to size hierarchies among siblings already established due to hatching asynchrony, and resultant competitive asymmetries often lead to starvation of the weakest nestling within a brood. The costs in terms of chick mortality can be high. However, the extent to which this mortality is egg size‐mediated remains unclear, especially in relation to hatching asynchrony which may operate concomitantly. I assessed effects of egg size and hatching asynchrony on nestling development and survival of Herring Gulls (Larus argentatus), where the smaller size and later hatching of c‐eggs may represent a brood‐reduction strategy. To analyze variation in egg size, I recorded the laying order and laying date of 870 eggs in 290 three‐egg clutches over a 3‐yr period (2010–2012). I measured hatchlings and monitored growth and survival of 130 chicks from enclosed nests in 2011 and 2012. The negative effect of laying date (β = ?0.18 ± SE 0.06, P = 0.002) on c‐egg size possibly reflected the fact that late breeders were either low quality or inexperienced females. The mass, size, and condition of hatchling Herring Gulls were positively related to egg size (all P < 0.0001). C‐chicks suffered from increased mortality risk during the first 12 d, identified as the brood‐reduction period in my study population. Although intraclutch variation in egg size was not directly related to patterns of chick mortality, I found that smaller relative egg size interactively increased differences in relative body condition of nestlings, primarily brought about by the degree of hatching asynchrony during this brood‐reduction period. Thus, the value of relatively small c‐eggs in Herring Gulls may lie in reinforcing brood reduction through effects on nestling body condition. A reproductive strategy Herring Gulls might have adopted to maintain a three‐egg clutch, but that also enables them to adjust the number of chicks they rear relative to the prevailing environmental conditions and to their own condition during the nestling stage.     

Shiny cowbird Molothrus bonariensis egg size and chick growth vary between two hosts that differ markedly in body size

In birds, egg size affects chick growth and survival and it is an important component of reproductive success. The shiny cowbird Molothrus bonariensis is an extreme generalist brood parasite that uses hosts with a wide range of body masses. Survival of cowbird chicks decreases with host body mass, as competition for food with nestmates is more intense in large than in small hosts. We studied variation in shiny cowbird egg size and chick growth in two hosts that differ markedly in body size: the chalk‐browed mockingbird Mimus saturninus (70–75 g), and the house wren Troglodytes aedon (12–13 g). We analyzed: 1) if females parasitizing mockingbirds lay larger eggs than those parasitizing wrens, and 2) the association between egg size and chick growth. We experimentally controlled for time of parasitism and number of host chicks and evaluated growth rate of male and female parasite chicks. Shiny cowbirds parasitizing mockingbird nests laid larger eggs than those parasitizing wren nests. Chick body mass after hatching was positively associated with egg size until chicks were five days of age, but there was no association between egg size and growth rate, or asymptotic mass. There were no sexual differences in egg size or body mass at the time of hatching, but growth rate was higher in males than in females leading to sexual dimorphism in asymptotic mass. Differences in egg size between hosts and the effect of egg size on body mass after hatching support the hypothesis that different females are specialized in the use of hosts that differ in body mass.     

Seasonal variation in reproductive measures of tropical Roseate Terns Sterna dougallih previously undescribed breeding patterns in a seabird

Seasonal variation in egg-laying, egg size, hatching success, hatchling mass, fledging success and chick growth of Roseate Terms Sterna dougallii breeding on Aride Island (Seychelles), Indian Ocean, were studied in 1997 and 1998. I investigated to what extent two patterns, common in a range of species, were followed by tropical Roseate Terns: (a) seasonal decrease in clutch size, egg size and breeding success and (b) an increase in breeding success with increasing egg weight. In 1997 (a poor year), the earliest nesting birds laid significantly smaller eggs, and chicks were lighter at hatching than those of peak nesting birds. The mean clutch size, of 1.04 eggs, showed no seasonal variation and no 'b'-eggs hatched. In 1998 (a good year) the earliest nesting birds laid eggs of similar size and their chicks were of similar weight to those of peak nesting birds. Mean clutch size, of 1.25 eggs, increased significantly through the season and about 60% of the 'b'-eggs hatched. In 1997, hatching success was 57% whereas in 1998 it was 80%. In both years, breeding success declined significantly through the season. The fact that the earliest breeding birds laid smaller eggs in a poor year and smaller clutches in a good year is in marked contrast to a range of other species, and to temperate-nesting Roseate Terns. Egg volume explained about half of the variance in hatchling mass in both years, but only 15% of the variation in linear growth rate. Hatching date was the only variable with a significant effect on fledging success. Roseate Terns on Aride seemed to sacrifice egg size and clutch size for earliness of laying. Presumably it is a strategy of older birds to lay as early as possible and may be regarded as a response of tropical Roseate Terns to breeding under relatively poor, and seasonally declining, food conditions.     

Breeding ecology of Red‐faced Cormorants in the Pribilof Islands,Alaska

ABSTRACT Red‐faced Cormorants (Phalacrocorax urile) are North Pacific endemics recognized as a vulnerable species, but little is known about their breeding ecology. We studied Red‐faced Cormorants on St. Paul Island, Alaska, from 1975 to 2009, with more detailed data collected in 2004 and 2005. Mean clutch sizes in 2004 (3.2 ± 0.8 [SD] eggs) and 2005 (3.1 ± 0.8 eggs) were similar to the long‐term average (2.9 ± 0.3 eggs from 1976 to 2009). The mean laying interval in 2004 and 2005 was 2.15 ± 0.80 d (N= 407), and the mean egg period (number of days between laying of an egg and hatching) was 31.1 ± 1.4 d (N= 158). Approximately 64 ± 17% of eggs hatched during the period from 1975 to 2009. The mean number of chicks per nest in 2004 and 2005 was 2.8 ± 0.8 (N= 232), and the mean number of fledglings per initiated nest in all years was 1.22 ± 0.52. Chicks fledged 46 to 66 d posthatching. In 2004 and 2005, the primary causes of egg loss were predation by Arctic foxes (Vulpes lagopus) and destruction of eggs and abandonment of nests due to storms. Starvation was the primary cause of nestling mortality in both years. Because chicks are dependent on parents to provide food for over 45 d, consistent near‐shore foraging opportunities must be available. From 1975 to 2009, Red‐faced Cormorants experienced only 1 yr of complete reproductive failure (1984). The consistent reproductive success of Red‐faced Cormorants suggests that conditions may be relatively stable for this species on St. Paul Island, or that the variability in their breeding ecology (e.g., phenology, clutch sizes, and incubation strategies) provides the flexibility needed to successfully fledge some chicks nearly every year.     

Testing the relationship between clutch size and brood size in the Coot (Fulica atra)

The time between egg laying and chick fledging is of crucial importance for the survival of young birds. I analyzed breeding output at consecutive phases of growth of young Coots (Fulica atra) relative to the clutch size and laying date. Considering the specific breeding biology of the Coot, I tested whether chick survival reveals clutch size-dependent variability. Clutch size did not affect hatching success; it only affected brood size, and that merely temporarily. During the first 20 days after hatching, i.e. during the time of the highest chick mortality, birds with larger clutches lost chicks at a higher rate. As a result, the number of fledged chicks was independent of the initial number of chicks, and pairs with different clutch sizes had a similar number of fledglings. The laying date had no effect. This pattern of age-related chick survival points to the greater role of the type of chick growth (semi-precocial) and behavior in their survival.     

VARIATION IN THE CAPPED WHEATEAR

Williams, A. J. 1980. Aspects of the breeding biology of the Subantarctic Skua at Marion Island. Ostrich 51:160-167.

The breeding biology of the Subantarctic Skua Catharacta antarctica lonnbergi was studied in two austral summers at Marion Island. Eggs were laid between 23 October and 19 December. The clutch size was one (6%) or two (94%) eggs. The laying interval was two (20%) or three (80%) days and the incubation period was 29 days. Chicks could fly at 50–65 days after hatching. Chicks from first and second hatched eggs in the same brood had similar growth rates. Chicks in one- and two-chick broods had similar growth rates until 50 days after hatching when chicks reared singly were heavier. Egg mortality was 15,8%, chick mortality was 34,8% and the overall breeding success was 50,9%. The results are discussed in comparison with previous studies of Subantarctic and South Polar C. maccormicki Skuas.     

Declining egg viability explains higher hatching failure in a suburban population of the threatened Florida scrub‐jay Aphelocoma coerulescens

Hatching failure occurs in approximately 10% of all avian eggs, but varies both within and among species. This reduction in viable offspring can have significant fitness consequences for breeding parents; therefore, it is important to understand which factors influence variation in hatching failure among populations. Previous research suggests that hatching failure is higher in a suburban than in a wildland population in the Florida scrub‐jay. From 2003 to 2007, we performed two experiments to examine whether increased hatching failure in the suburbs resulted from 1) increased length of off‐bouts during incubation (predation risk hypothesis, 2003–2004) or 2) increased exposure to ambient temperature during laying (egg viability hypothesis, 2005–2007). Hatching failure was higher for females that took fewer off‐bouts, but the length of those off‐bouts did not influence hatching failure. Thus, nest predation risk does not appear to explain higher hatching failure in the suburbs. Alternatively, hatching failure increased with increasing exposure of eggs to ambient conditions during the laying period. First‐laid eggs in the suburbs had the greatest pre‐incubation exposure to ambient temperature and the greatest rate of hatching failure, consistent with the egg viability hypothesis. Urbanization influences hatching failure through a series of complex interactions. Access to predictable food sources advances mean laying date in suburban scrub‐jays, leading to larger clutch sizes. Because scrub‐jays begin incubation with the ultimate egg, first‐laid eggs in the suburbs may be exposed to ambient temperatures for longer periods, thus reducing their viability.     

Reproductive success of wild Lesser Rheas (Pterocnemia -Rhea- pennata pennata) in north-western Patagonia, Argentina

We studied the reproductive success of a wild Lesser Rhea population (Pterocnemia -Rhea- pennata pennata) during two reproductive seasons (2004/2005 and 2005/2006) in north-western Patagonia, Argentina. The parameters recorded included population and nest density, clutch size, hatching success, chick survival (up to 3 months of age) and percentage of chicks that reached the juvenile stage after the winter. We also estimated the percentage of males that attempted to nest and of those that were successful (those producing at least one chick), daily nest mortality rates (DNMR) at different stages of the nesting cycle and the probability that an egg that has been recently laid will produce a chick. On average, both years pooled, the density of this population of Lesser Rheas was 1.55 ± 0.2 individuals/km² (SE), nest density was 0.17 ± 0.04 per km ² , clutch size was 20.8 ± 6.4 eggs, hatching success was 74.4% ± 11.3, Mayfield’s probability of an egg that will produce a chick was 0.64, chick survival was 65.4% ± 14.5 and percentage of chicks that reached the juvenile stage was 26.3%. Nearly a quarter of Lesser Rhea males in the population attempted to nest during a breeding season, and the DNMR was significantly higher during the laying stage (most nest failures were due to anthropogenic disturbances related to livestock raising activities). Nesting success, hatching success, and chick survival of Lesser Rheas were higher than those of their most closely related species, the Greater Rhea (Rhea americana), whereas the percentage of chicks that reached the juvenile stage was similar due to high winter mortalities of chicks. We suggest that the increase in reproductive effort is a strategy of this species to overcome environmental constraints.     

Intraspecific variation in reproductive traits of burrowing owls

Reviews of hatching asynchrony in birds recommended more studies on intraspecific variation in the extent of hatching asynchrony. We examined intraspecific variation in clutch size, laying chronology, onset of incubation, incubation period, and hatching asynchrony in burrowing owls (Athene cunicularia) in the Imperial Valley of California. Mean clutch size was 7.4 eggs and owls averaged 0.5 eggs laid per day. Females varied considerably in laying interval and onset of incubation (range?=?1st to 9th egg in the clutch). The mean incubation period was 21.9?days. Hatching interval also varied greatly among females ( $ \overline{x} $ ?=?0.8, range 0.1–2.0?days between successively hatched eggs). Past burrowing owl studies have largely overlooked the substantial intraspecific variation in these traits or have reported estimates that differ from ours. Future studies designed to identify the environmental factors that explain the large intraspecific variation in these traits will likely provide insights into the constraints on local abundance.     

Breeding biology of the thin-billed prion<Emphasis Type="Italic"> Pachyptila belcheri</Emphasis> at New Island,Falkland Islands: egg desertion,breeding success and chick provisioning in the poor season 2002/2003

We present data on breeding success, chick growth and chick feeding in thin-billed prions, Pachyptila belcheri, at New Island, Falkland Islands, in the breeding season 2002/2003. As in many populations of seabirds in the region, the overall breeding success was very low. This was mainly caused by low rate of observed burrow occupancy (60%) and hatching (57%) of thin-billed prions, while chick survival was closer to normal. Sixty-eight percent of the chicks survived to fledging. In total, a chick was successfully reared in 23% of the nests or from 38% of recorded eggs. The failed eggs were found to be incubated for 30 days, on average. The time of egg desertion coincided with the time of desertion of other seabirds at New Island, with a period of high sea-surface temperatures and low catch rates by the commercial fisheries. We describe chick growth and use repeated weighings, corrected for metabolic loss, to estimate meal sizes. Chicks were fed a mean 39.2 g in 77% of the nights. We discuss possible reasons for the observed extremely low hatching success, and compare with the breeding success of other seabirds at the Falkland Islands.     

Drivers of the breeding success of American Oystercatchers (Haematopus palliatus frazari) at a critical site in Sinaloa,Mexico

Understanding breeding phenology and success can elucidate population dynamics, which is especially important for species in need of conservation. We describe the factors affecting the breeding biology of American Oystercatchers (Haematopus palliatus frazari) at El Rancho Island, a critical site that contains ~ 7% of the total estimated population, on the coast of Sinaloa, Mexico. We monitored 192 nests over four years (2016–2019). The breeding season lasted from March to June and mean laying dates differed among years, with the mean laying date in 2019 an average of 20 days earlier than in 2016. Clutch sizes decreased as the breeding season progressed. Both breeding success and productivity differed among years, with the lowest values in 2016 (30% hatching success and 0.6 chicks/nest) and the highest in 2019 (66% hatching success and 1.2 chicks/nest). Hatching success was affected by year, laying date, type of habitat, and distance to the high tide line. American Oystercatchers that laid eggs earlier in the season, used mixed marsh and dune habitat, and with nests relatively close to the waterline (< 50 m) had greater breeding success. Overall, however, the breeding success of American Oystercatchers was low and influenced by a combination of several intrinsic and extrinsic factors. Management measures may be required to increase breeding success and ensure the conservation of this subspecies.     

Incubation prior to clutch completion accelerates embryonic development and so hatch date for eggs laid earlier in a clutch in the great tit Parus major

The ability of parents to respond to changes in food supply within a season will have a large effect on fitness through the number and quality of chicks fledged. Great tits, Parus major, attempt to synchronise their production of chicks with a seasonal food peak, but when food supply fails, hatching asynchrony of chicks provides a mechanism by which some young can be fledged because more developed chicks outcompete their less developed siblings for the reduced parental food supply. We tested whether female great tits can potentially control the degree of hatching asynchrony by using incubation before clutch completion, so that early laid eggs develop faster and hatch sooner. The temperature of an artificial egg placed in 29 nests during the laying period was measured with data loggers, and nocturnal incubation of eggs similar to incubation post clutch completion was recorded in all nests. We then demonstrated that eggs removed from the nest for 72 hour periods prior to clutch completion hatched later than eggs remaining in the nest for the entirety of the laying period. Our results show that variable pre clutch completion incubation (which was mostly nocturnal) can lead to faster embryo development and earlier hatching, so potentially providing a mechanism for adaptive female control of degree of hatching asynchrony.     

Immunity, growth and begging behaviour of nestling Barn Swallows Hirundo rustica in relation to hatching order

In altricial birds, asynchronous hatching often results in a size hierarchy among nestlings. However, laying order and hatching order may affect components of offspring condition differentially. Since parasites can have a heavy impact on their hosts, strategies may have evolved that allow parents and offspring to allocate critical resources to immunity depending on hatching order. In this study of the Barn Swallow Hirundo rustica we (1) analyse the relationship between laying and hatching order of eggs, (2) compare morphological, serological and immunological traits between early- and late-hatched siblings, and (3) compare the begging behaviour of early- and late-hatched nestlings. Hatching order strictly reflected laying order. Late-hatched chicks begged more for food but had smaller body mass throughout the nestling period. Immunoglobulin concentration and intensity of T cell-mediated immunity were larger in late-hatched nestlings. Large concentration of immunoglobulins in late-hatched nestlings may reflect transfer of immunity from the mother via the egg. Alternatively, in association with larger T cell-mediated immunity, immunoglobulin production may indicate larger investment in immunity by late-hatched nestlings. Laying order and hatching order may therefore affect components of nestling condition differentially.     

THE LAYING INTERVAL AND INCUBATION PERIOD OF ROCKHOPPER AND MACARONI PENGUINS

Williams, A. J. 1981. The laying interval and incubation period of Rockhopper and Macaroni Penguins. Ostrich 52: 226–229.

The laying interval and incubation period of Rockhopper Penguins Eudyptes chrysocome and Macaroni Penguins E. chrysolophus were studied at Marion Island in 1974–75 and 1976–77. On average, the laying interval was 4,4 and 4,5 days, the incubation period of second-laid eggs was 34,2 and 35,9 days and that of first-laid eggs was 39,1 and 38,0 days in Rock-hopper and Macaroni Penguins respectively. The laying interval in this genus is longer than that in other penguins. The incubation period is similar to that of most other penguins but the second-laid egg normally hatches before the first-laid egg. The long laying interval and the hatching sequence of the eggs both have important affects upon the mortality of eggs in the genus Eudyptes.     

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.