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.     

The breeding biology and factors affecting reproductive success in rockhopper penguins <Emphasis Type="Italic">Eudyptes chrysocome</Emphasis> at Macquarie Island

Adult mass changes, egg morphometrics, chick growth rates, fledging masses, reproductive success and reasons for reproductive failure were examined in rockhopper penguins at Macquarie Island from 1993/1994 to 1995/1996. Mean arrival masses, growth rates of chicks and fledging masses exhibited inter-annual variability, while egg morphometrics, hatching success (68.0±6.0%) and reproductive success (47.3±8.3%) were constant between years. Reproductive failures occurred primarily during incubation, with the majority of eggs lost to great skuas. Logistic regressions revealed that no variable significantly explained hatching success, and only in 1994/1995 was fledging success significantly correlated with the position of nest in the colony (those in the centre were more successful than those on the periphery). Reproductive success during this study was relatively high, and therefore an assessment during poor years would be instructive, particularly in relation to aspects of the penguins’ foraging ecology.     

Estimating the home range and carrying capacity for takahe (

Predator-free offshore islands play an important role in the conservation of many of New Zealand's endemic species. Takahe (Porphyrio mantelli) have small populations established on four offshore islands and although hatching success is lower than that of the wild mainland population in Fiordland, juvenile and adult survival is high and populations are growing exponentially. Accurate estimates of home range size and potential carrying capacities are therefore essential for the future management of the population as a whole. The mean home range size of takahe pairs in one study population on Mana Island (217 ha) was 2.8 ± 1.9 ha. The island was assessed for current and maximum available area for takahe and the potential carrying capacity was estimated at 22—53 pairs. Current and maximum available areas were also used to calculate carrying capacities on each of three other islands using two different estimates of mean home range size for Maud Island (7—34 pairs) and Kapiti Island (5—33 pairs) and one estimate of home range size for Tiritiri Matangi Island (25 pairs). A model of the population growth of takahe on islands predicted that estimated carrying capacities would be reached between 1997 and 2009. The urgency of planning to make use of the considerable potential of island populations of takahe is stressed.     

Demography of takahe (

The last remaining natural population of the critically endangered takahe (Porphyrio hochstetteri) is confined to the Murchison Mountains in Fiordland, New Zealand. This mainland population contains about half of the c.?300 remaining takahe and benefits from one of the costliest recovery programmes in the country. Management activities include deer culling, stoat trapping, nest manipulation (e.g. removal of infertile eggs) and captive rearing of chicks. To determine what effect this intensive management has had on the recovery of the Fiordland takahe population, we modelled 25 years of survival and breeding success data as a function of environmental factors (e.g. precipitation, temperature, beech seedfall, tussock flowering) and specific management activities (egg manipulation, captive rearing, stoat control). Annual adult survival, estimated at 78% (credibility interval (CI) = 75?81%), is significantly increased to 85% (76?92% CI) in presence of stoat trapping, but is still low relative to introduced takahe populations on offshore islands and other large New Zealand bird species in predator-free environments. This suggests that the harsh environment of Fiordland may be suboptimal habitat in terms of survival for takahe. On the other hand, reproductive output in Fiordland is similar to that for introduced island populations, and is improved even further by management. Number of chicks per pair fledged with nest manipulation and captive rearing is estimated at 0.66 compared with 0.43 in the absence of nest management. The difference is explained mainly by low fledging success in the wild, especially for double clutches, which justifies the practice of removing one of two viable eggs and transferring it to a captive-rearing facility. The results of this study indicate that current management activities such as stoat trapping and captive rearing have a strong positive effect on population growth of the Murchison Mountains takahe population.     

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.     

Testicular and spermatozoan parameters in the pukeko (Porphyrio porphyrio melanotus)

The pukeko (Porphyrio porphyrio melanotus) is widespread in New Zealand, and is the closest living relative to the endangered takahe (Porphyrio mantelli), which has a relatively high rate of infertility. In this study, sperm collected from a number of pukeko was analysed in order to model the reproductive physiology of the male takahe. In addition, testicular parameters were measured. To ascertain the best method of sperm collection five techniques for harvesting sperm were used on two occasions during the breeding season. All five techniques resulted in the successful recovery of sperm. However, the float-out technique produced the best quality samples. Following collection, the morphometry of unstained sperm was assessed. Our findings suggest that pukeko sperm is non-motile in the male reproductive tract. We found the mean sperm head length in the pukeko is 16.9mum, but sperm head length varied significantly between birds. Testicular weight and length was significantly correlated with bird weight (P<0.05). Within each bird, testes weights were asymmetric. However, testes length was significantly correlated (P<0.05). There was a significant difference (P<0.05) in testes length between birds. The methodologies presented for obtaining and analysing pukeko sperm morphometry can be used to assist opportunistic studies of the reproductive biology of other New Zealand native birds.     

Individual quality and reproductive performance in the Grey-headed Albatross Diomedea chrysostoma

The reproductive performances of Grey-headed Albatrosses Diomedea chrysostoma with a previous record (≤5 years) of consistent success (≤70% chicks fledged from eggs laid—"top" birds) or failure (≤ 70% of attempts failed—"bottom" birds) were compared during 1993 -1995. In 1995, top birds arrived back at the colony significantly earlier, had significantly shorter first and second incubation shifts and hatched larger chicks which grew significantly faster than bottom birds. In 1994, top birds also had larger hatchlings with higher rates of growth than bottom birds. In 1994, top birds had significantly higher hatching, fledging and therefore overall breeding success than bottom birds; very similar trends were evident in 1993 and 1995. Chick-rearing success and all indices of chick growth suggested that food availability was high in 1995 (and 1993) and low in 1994. Therefore the superior performance of top birds was maintained in years of very different conditions, with the chick-rearing period particularly critical. A simple model (using published demographic parameters for Grey-headed Albatrosses on South Georgia) suggests that top birds would produce 2.5 more chicks over their lifetime than bottom birds. With the currently declining population numbers, the relative contribution of top birds to the next generation may be even greater than this.     

Proceedings of the New Zealand Society for Parasitology Inc.

Abstract

A study of the nesting habits and breeding biology of blue penguin Eudyptula minor was undertaken over the 1995–96 and 1996–97 breeding seasons on Matiu‐Somes Island, Wellington, New Zealand. Male and female blue penguins tended to be faithful to both mates and nest sites, although there was insufficient evidence to detect any association between a bird's breeding success in 1995 and a subsequent change of mate or nest in 1996. Over the 1995 and 1996 seasons the recorded hatching success (0.51 ±0.11 and 0.63 ± 0.10 respectively), fledging success (0.81 ±0.12 and 0.85 ±0.10 respectively) and reproductive success (0.41 + 0.11 and 0.54 ± 0.11 respectively) were similar each season. There was no significant difference between the proportion of eggs laid, or eggs hatched and chicks fledged, between the two seasons. The mean number of chicks raised over the two seasons was 0.94 ± 0.05 per nest. Replacement clutches were laid by 11 per cent of failed breeders in each season, but only in 1996 were they successful in fledging chicks.

No significant difference was found between the breeding success of the Matiu‐Somes Island blue penguin colony recorded during this study and a previous study undertaken on the island 40 years ago.     

Egg-size variation and reproductive success in the Herring Gull Lams argentatus: adaptive or constrained size of the last egg?

Herring Gull Larus argentatus eggs from a study colony in the Baltic showed a slight but significant variation in egg size within the laying sequence. Last-laid eggs were only about 5% smaller by volume than first eggs. There was no significant difference in dry yolk weight or dry albumen weight, although possible differences were evident. The chicks had nearly equal hatching weights and equally long tarsi. There was no differential mortality in the third chick in the study colony, and there were no indications of egg-size-mediated mortality. The birds in the colony produced an average of 1.45 fledglings per pair. Compared with several other studied colonies, the difference in egg size within a clutch was low, and a comparison of colonies from northwestern Europe suggests that variance within the clutch is negatively correlated with fledging success, so that a large difference in size between first and last eggs is associated with low fledging success. We suggest that the size of the last egg in the clutch reflects the feeding potential in the environment and is mainly a nonadaptive response to poor feeding conditions during laying.     

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.     

ASPECTS OF McCORMICK SKUA BREEDING BIOLOGY

The breeding behaviour of the McCormick Skua was studied at Cape Royds, Antarctica, for three summers. These observations followed the work of Young (1963a, b). Records of banded birds suggest that at the age of five to six years birds return to breed in the area where they were reared. Breeding pairs retain the same territory and mate over consecutive summers. The male will retain a territory and remate if the female does not return, while there is some evidence to suggest that if the male is absent the female will leave the territory and remate elsewhere. Unfavourable weather frequently forced incubating birds to desert their eggs and as a result some pairs laid three clutches (at the most two clutches of two eggs and a clutch of one). The death of sibling chicks from fighting was examined by comparing the early growth of 11 successful pairs of chicks with that of 12 pairs in which one of the siblings died as a result of fighting. From a comparison of weights at hatching and the interval between the hatching of members of chick pairs, it appears that the difference in weight between twins and the gain in weight by one chick in the first few days is critical for the survival of the twins. The breeding success, calculated from the total eggs laid and the total number of chicks fledging, was 40%, 42% and 17% for the three respective summers. Storms (periods of wind with snow) were the main factor influencing breeding success.     

Chick loss in the Falkland Skua Catharacta skua antarctica

Data on reproductive success of 110 Falkland Skua Catharacta skua antarctica pairs were gathered during the austral summers of 1988–1989 and 1990–1991 on New Island, Falkland Islands. Adults laid two eggs 2–3 days apart and began incubation with the first egg. For the years combined, 1.39 chicks per nest hatched and 0.84 chicks per nest fledged (fledging was defined as surviving to 16 days of age). Brood reduction was common; 43% of the two-chick broods were reduced to one, and mortality was concentrated on the younger chick. Although asynchronous hatching and differential death are consistent with Lack's brood reduction hypothesis, application of O'Connor's quantitative criterion revealed that sibling competition may not be responsible for the observed chick mortality. Furthermore, because no aggressive interactions between chicks were observed or detected indirectly, siblicide may be absent in this population. Instead, predation modified by a variety of factors may have led to the greater mortality of the second-hatched chick.     

Variations in growth of Cape petrel Daption capense chicks

This study reports on the growth of Cape petrel chicks at Nelson Island, South Shetland Islands, Antarctica, during the breeding seasons 1990/91 and 1991/92. Parameters of logistic growth model fitted to mass, wing, culmen and tarsus measurements were compared between available composite data sets. Differential growth rate of morphometric characters and their proportional development at hatching and fledging conform to the pattern observed in other fulmarine petrels, overall growth rate being among the fastest found in Procellariiformes. Composite growth curves varied significantly between populations, but few annual, seasonal, and intercolony differences were found within the Nelson Island population. As the differences between chicks from equally disturbed colonies were less marked than in comparison with the control colony, regular handling most probably reduced the growth in this study. Larger eggs produced heavier rather than structurally larger hatchlings, which attained higher peak and fledging mass and size. Strength of the relationship between egg-size and chick measurements initially declined with chick age but, in contrast with results of earlier studies, increased again after around the middle of the chick-rearing period. This suggests that pre-hatching maternal factors probably influenced initial and fledging (peak) size and mass of chicks via egg-size, while intermediate stages of growth were less affected. A difference in mass between chicks from small and large eggs was maintained until fledging and increased gradually until peak mass was reached.     

Rates and consequences of relaying in Cassin's auklets Ptychoramphus aleuticus and rhinoceros auklets Cerorhinca monocerata breeding in a seasonal environment

We removed first eggs from early‐laying females to measure rates and consequences of relaying in Cassin's auklets Ptychoramphus aleuticus and rhinoceros auklets Cerorhinca monocerata at Triangle Island, British Columbia, Canada. Based on egg size and composition, the investment that Cassin's auklets made in first eggs was very close to that predicted from adult body mass, whereas rhinoceros auklets invested more. In both species, a high percentage of females relaid (90% of Cassin's and 87% of rhinoceros auklets). Breeding success declined weakly with later laying among control Cassin's auklet pairs, but pairs that we induced to relay bred more successfully than naturally late pairs, and similar to values predicted from laying dates of their first eggs. Their chicks also fledged heavier and younger than late control chicks, and similar to values in early control chicks, but followed the population‐wide seasonal decline in wing length at fledging. Nestling diets were dominated by Neocalanus copepods until late in the season, a sign that feeding conditions remained favourable until late. In contrast, rhinoceros auklet pairs induced to relay followed the population‐wide seasonal decline in breeding success, which was driven by a decline in hatching success. Pacific sandlance Ammodytes hexapterus, thought to be a preferred prey species, virtually disappeared from nestling diets in mid‐to‐late season, yet there was no seasonal decline in fledging mass. However, chicks from replacement eggs followed the declines among control chicks in both age and wing length at fledging. Despite the female having produced a replacement egg, and despite delayed breeding, there appeared to be little immediate consequence associated with relaying for Cassin's auklets, except for a tendency for their chicks to fledge with short wings. Consequences were more marked in rhinoceros auklets (greatly reduced hatching success, and having their chicks fledge with short wings), and this may have been due to the large investment made in eggs, and/or to delayed breeding. Results of this study show that attributes of Cassin's and rhinoceros auklets that lay at different times in the season can be important in driving seasonal declines in breeding performance, as found in studies on other Alcidae. They also show how decisions taken during the egg stage can have variable yet potentially important implications for fitness, even in relatively long‐lived species that lay single‐egg clutches.     

Experimentally Constrained Virulence is Costly for Common Cuckoo Chicks

Chicks of some avian brood parasites show high virulence by eliminating all host progeny in the nest whereas others develop in the presence of host nestmates. Common cuckoo ( Cuculus canorus ) chicks are typically highly virulent parasites as they attempt to evict all host eggs and chicks soon after hatching. However, several features of nest design, including steep walls and/or cavity nests, may effectively prevent cuckoo hatchlings from evicting nestmates. A previous observational study showed low success of cuckoo chicks in evicting progeny of a cavity nester host, the redstart ( Phoenicurus phoenicurus ) but cuckoo chicks showed low survival both when reared alone or in mixed broods with host nestmates. Whether poor cuckoo performance was caused by eviction costs and/or by the effect of presence of host chicks per se remains unclear. We experimentally cancelled any potential eviction costs by removing host eggs immediately after the cuckoo hatched and creating mixed broods 5 days later when the eviction instinct of the cuckoo already ceased. Cuckoos that were forced to compete with host nestlings experienced lower provisioning rates, poorer growth, and lower fledging success than control lone cuckoos. Cuckoos in mixed broods that survived until fledging fledged later, and at lower masses, than those in the sole cuckoo group. Thus, the cuckoo gens specializing on redstarts is similar to other cuckoo gentes, whose chicks are more successful in evicting host nestmates, and it does not benefit from the presence of host brood. Cohabitation with host nestlings then should be viewed as a maladaptive by-product of host cavity nest design.     

Breeding biology of the Barn Owl Tyto alba in central Mali

Data were obtained on 178 clutches of African Barn Owls in central Mali from four breeding seasons during 1979–1983. Significantly more clutches were laid in 1979–1980 and significantly fewer in 1980– 1981 than the average for the 4 years and there were significantly more clutches laid in the middle period of the annual breeding season. The egg volume was significantly smaller at the beginning of the breeding season and significantly larger in the middle than the overall mean with eggs of second clutches being larger than those of first clutches. The clutch size was 605 eggs of which 479 hatched. The number of young fledged per successful nest was 319 and was 1 83 for all nesting attempts. The month was the only variable shown to affect significantly the clutch size, eggs hatched and fledging rate, the highest success rates being associated with the middle of the breeding period. The average interval between the hatching of eggs was 2–31 days. Survival rates (47'1%) to fledging were significantly affected by year (1981–1982 being the least) and month (mid-season birds the best). The order of hatching significantly affected age at death or disappearance, the first-hatched birds surviving the longest. The year significantly affected age at fledging, the young from the year in which most clutches were laid leaving the nest at the youngest age and those associated with the year having the least number of clutches remaining in the nest the longest. The month of hatching also affected fledging age, birds at the extremes of the breeding season fledging at older ages. The discussion compares these data with those from elsewhere.     

Timing of fledging is influenced by glucocorticoid physiology in Laysan Albatross chicks

Fledging is a major life transition for birds, when juveniles move from the safety of a nest into an environment where they must find food and avoid predators. The timing of fledging within a season can have significant effects on future survival and breeding success. Proximate triggers of fledging are unknown: though wing development is likely a primary factor, other physiological changes, such as elevated plasma corticosterone (CORT), may affect fledging behavior. Laysan Albatross (Phoebastria immutabilis) chicks have an extended post−hatching period during which they reach 150% of adult mass. However, approaching fledging, chicks fast for days to weeks and lose mass while still putting energy into feather growth. We evaluated chick morphology and physiology to elucidate proximate triggers of fledging. As in some other species, CORT increased as chicks fasted and lost body mass. At the same time, corticosteroid binding globulin (CBG) declined, thus amplifying free CORT prior to fledging. Once chicks reached a morphological threshold, free CORT levels predicted how long they stayed at the colony: chicks with higher free CORT fledged sooner. To perturb the relationship between body condition, endocrine physiology, and fledging behavior, we supplementally fed chicks for the month before fledging. Fed birds had a slower decrease in body mass, slower decrease in CBG, slower increase in free CORT, and stayed at the colony longer after reaching a morphological threshold. Our study suggests that as chicks lose mass, free CORT acts as a signal of energetic or nutritional state to adjust the timing of fledging.     

Are corticosterone levels a good indicator of food availability and reproductive performance in a kittiwake colony?

We evaluated the use of corticosterone to gauge forage availability and predict reproductive performance in black-legged kittiwakes (Rissa tridactyla) breeding in Alaska during 1999 and 2000. We modeled the relationship between baseline levels of corticosterone and a suite of individual and temporal characteristics of the sampled birds. We also provided supplemental food to a sample of pairs and compared their corticosterone levels with that of pairs that were not fed. Corticosterone levels were a good predictor of forage availability in some situations, although inconsistencies between corticosterone levels and reproductive performance of fed and unfed kittiwakes suggested that this was not always the case. In general, higher corticosterone levels were found in birds that lacked breeding experience and in birds sampled shortly after arriving from their wintering grounds. All parameters investigated, however, explained only a small proportion of the variance in corticosterone levels. We also investigated whether corticosterone, supplemental feeding, year of the study, breeding experience, body weight, and sex of a bird were able to predict laying, hatching, and fledging success in kittiwakes. Here, breeding experience, year of the study, and body weight were the best predictors of a bird's performance. Corticosterone level and supplemental feeding were good predictors of kittiwake reproductive performance in some cases. For example, corticosterone levels of birds sampled during the arrival stage reliably predicted laying success, but were less reliable at predicting hatching and fledging success. Counts of active nests with eggs or chicks may be more reliable estimates of the actual productivity of the colony. Supplemental feeding had strong effects on kittiwake productivity when natural forage was poor, but had little effect when natural forage was plentiful.     

Experimental manipulation of female reproduction reveals an intraspecific egg size-clutch size trade-off

A negative relationship, or trade-off, between egg size and clutch size is a central and long-standing component of life-history theory, yet there is little empirical evidence for such a trade-off, especially at the intraspecific level. Here, I show that female zebra finches (Taeniopygia guttata) treated chronically during egg formation with the anti-oestrogen tamoxifen lay smaller eggs (by 8%) but produce larger clutches (on average two eggs more) than controls. Decreased egg mass in tamoxifen-treated females was associated with a 50% decrease in plasma levels of the two yolk precursors, vitellogenin and very-low-density lipoprotein. Although tamoxifen-treated females laid more, smaller eggs (and had a higher total expenditure in their clutch), they did not differ from controls in the number of chicks fledged, the mass or size of these chicks at fledging, or the chicks' egg-production performance at three months of age. However, tamoxifen-treated females had lower relative hatching success: they laid more eggs but hatched the same number of chicks. Among individual tamoxifen-treated females, birds that laid the smallest eggs early in their laying sequence laid the largest number of additional eggs, that is, there was a negative correlation, or trade-off, between egg size and clutch size.     

Factors affecting breeding success of the Flea Bay white-flippered penguin (

The little blue penguin (Eudyptula minor) is in decline throughout much of its range in New?Zealand and Australia, largely due to introduced predators, human disturbance and roadkill mortalities. The white-flippered penguin is a unique morphological variant of the blue penguin, which is traditionally given subspecific status (Eudyptula minor albosignata), and is found only on Banks Peninsula and Motunau Island in Canterbury, New?Zealand. We monitored a varying number of nest boxes from 1996 to 2009. Overall breeding success was 64% over 13 years of monitoring, with a hatching success rate of 75% and a fledging success rate of 85%. We used a set of generalised linear mixed models and model selection to examine the relative influence of various explanatory variables on hatching, fledging and overall breeding success. Breeding success in nest boxes significantly increased with shorter average pair bond length, longer guard period and later relative lay date. Guard period length was the best predictor of breeding success, followed by relative lay date and average pair bond length. Hatching success also increased with later relative lay date but fledging success was not influenced by any of the explanatory variables measured.