One House Two Families: Petrel Squatters Get a Sniff of Low‐Cost Breeding Opportunities

Burrowing is a widespread nesting behaviour, found in vertebrates and invertebrates. It is particularly common in small procellariiform seabirds such as blue petrels (Halobaena caerulea) and Antarctic prions (Pachyptila desolata), two closely related petrel species. However, digging a burrow is costly and alternative strategies may evolve. Accordingly, blue petrel males can adopt two alternative nesting strategies: digging a new burrow or squatting in an empty one. Importantly, a blue petrel squatter arriving at the colony to breed is more likely to find empty Antarctic prion burrows than empty blue petrel burrows, since the former species only start breeding a month later. However, squatting in a prion’s burrow is risky for blue petrels as the legitimate owner very often returns and claims the burrow back, thus ruining the squatter’s breeding attempt. We present here results of a survey of two sympatric colonies of blue petrels and Antarctic prions on Kerguelen Island. Our data show that blue petrel squatters preferentially occupy blue petrel empty burrows. To investigate potential underlying mechanisms behind this preference, we used a simple Y‐maze design to show that blue petrels can discriminate and prefer their specific odour over the prion odour. Our results confirm the existence of alternative burrowing strategies in blue petrels and suggest that squatters could use olfaction to avoid the less suitable Antarctic prion burrows.     

Incorporation of marine-derived nutrients from petrel breeding colonies into stream food webs

1. Stable isotope ratios of aquatic invertebrates, aquatic mosses and leaves of riparian plants were used to determine whether marine‐derived nutrients from breeding colonies of the Westland petrel (Procellaria westlandica) were incorporated into the food webs of small streams in New Zealand. 2. The δ¹⁵N signatures of all plants and animals examined were higher by 3.6–4.6‰ in small streams draining catchments with petrel colonies than in nearby streams where petrels were absent. δ¹³C values of leaves from terrestrial plants were also enriched by about 2‰ where petrels were present, but the carbon ratios of aquatic species were depleted in ¹³C, rather than enriched, suggesting that any marine signal was over‐ridden by isotopic shifts related to photosynthetic fractionation. 3. A high marine‐nitrogen signal was maintained along the 3 km length of Scotchman Creek with the δ¹⁵N values of leptophlebiid mayflies and predatory insects ranging from 7.4–9.5 and 9.2–11.9‰, respectively. 4. Most nutrients derived from petrels are likely to be translocated to streams via the soil, which they enter in the form of excreta, spilled food, feathers, dead chicks, and abandoned eggs. However, because changes in δ¹⁵N values are brought about by soil processes such as volatilisation of ammonia, nitrification and denitrification, it is difficult to predict the exact isotope signature of nitrogen entering a stream. Tentative estimates of the proportion of marine‐derived nitrogen in stream biota, calculated using a mass‐balance approach, ranged from 28–38%. 5. Our findings indicate that marine nutrients transported inland by seabirds can be incorporated into the food webs of streams. In pre‐human times when there were many more seabird colonies on mainland New Zealand than exist today, marine‐derived nutrients introduced by birds may have had significant effects on nitrogen cycling and the productivity of New Zealand streams.     

Differences in habitat selection between Chatham petrels (

The Chatham petrel (Pterodroma axillaris) is an endangered species restricted to a single population on South East Island, Chatham Islands, New Zealand. The key threat to Chatham petrel breeding success is interference with chicks by broad-billed prions (Pachyptila vittata) prospecting for burrows for their oncoming breeding season. This burrow competition has resulted from alteration to breeding habitat by humans throughout the Chatham Islands. Understanding habitat preferences may enable managers to manipulate habitat to reduce burrow competition and will be essential in order to translocate Chatham petrels to a proposed second colony. Habitat characteristics surrounding both Chatham petrel and broad-billed prion burrows were quantified and selection ratios compared. Both Chatham petrels and broad-billed prions selected habitat factors associated with mature forest. Chatham petrels avoided a large number of habitat characteristics, which suggests they were habitat specific, and their preferred habitat is now limited. Broad- billed prions used a wide range of habitat characteristics, which suggests they are not habitat specific. This study recommends that selection values be used when deciding on the best location to establish a second Chatham petrel colony.     

The depth of Sooty Shearwater Ardenna grisea burrows varies with habitat and increases with competition for space

The Sooty Shearwater Ardenna grisea, an abundant but declining petrel, is one of many seabird species that construct breeding burrows, presumably because these confer protection from predators and the elements. Little is known about the causes of variation in Sooty Shearwater burrow architecture, which can differ markedly both within and between breeding sites. We hypothesize that burrow architecture varies in response to habitat type and competition for space. To address these hypotheses, we recorded Sooty Shearwater burrow dimensions on Kidney Island, the largest Sooty Shearwater colony in the Falkland Islands, South Atlantic, and modelled these as functions of burrow density (a proxy for competition) and habitat indices. Our models suggest that Sooty Shearwaters burrow further underground in response to competition for breeding space, and that soil underlying dense tussac grass Poa flabellata is more easily excavated than other substrates, indicating how vegetation restoration could aid the conservation of this species.     

Changes in sooty shearwater (Puffinus griseus) abundance and harvesting on the Rakiura Titi Islands

Abstract

We estimated the change in abundance of sooty shearwater (titi, Puffinus griseus) at six Rakiura Titi Islands, New Zealand, by comparing historical and recent surveys of the density of entrances to breeding burrows. We found evidence that entrance density between 1994 and 2006 was lower than it was between 1961 and 1976. Our overall estimate of the annual rate of change in burrow entrance density is ‐1.0% (95% CI ‐2.3 to ‐ 0.1%). Declines have been slower on four islands where Rakiura Maori maintain a traditional harvest of sooty shearwater chicks ("muttonbirding") compared with three unharvested islands. Density‐dependent population processes may explain this difference: rates of decline have been faster in areas of relatively high initial entrance density, and historically the harvested islands have had lower initial density. There was a strong, apparently linear, relationship between entrance density and chick density on breeding colonies, so changes in entrance density probably do indicate a real population decline. The western side of Taukihepa, the largestof the Titi Islands, first became accessible for muttonbirding with the advent of helicopters in the 1970s, but it is unknown whether this has caused an increase in the number of sooty shearwaters harvested by Rakiura Maori.     

Predictive habitat modelling to estimate petrel breeding colony sizes: Sooty shearwaters (Puffinus griseus) and mottled petrels (Pterodroma inexpectata) on Whenua Hou Island

Abstract

Between 2001 and 2006, we systematically sampled the entire coast of Whenua Hou, a rugged offshore island in southern New Zealand, to estimate the population densities of sooty shearwaters (Puffinus griseus) and mottled petrels (Pterodroma inexpectata) by counting the entrances of breeding burrows. A two‐step regression modelling process using binomial errors was used to predict the presence of a colony, and a normal general linear model was used to predict the density of entrances within colonies. Aerial photography, GIS and a Digital Elevation Model were used to extract relevant habitat and location variables, and a combination of both regression models was used to predict the density of breeding burrows within each 5.32 m² pixel on the island. This complex GIS and habitat prediction modelling approach gave population estimates very similar to a more traditional simple area extrapolation method and gave no improvement in precision. However, correction for the slope of the land increased our simple area estimates of population size by 11%. We estimate populations of sooty shearwater and mottled petrel breeding pairs at 173 000 (162 000–190 000) and 160 000 (123 000–197 000) respectively. Based on this number of breeding pairs, we calculate that Whenua Hou supports a total population of 868 000 (554 000–1 270 000) sooty shearwaters. Our estimate of the total mottled petrel population 202 000 pairs (162 000–242 000) is comparable with the only published estimate, but could be an underestimate because mottled petrels are sometimes found in large burrows. More research for robust estimation of population trends is needed to assess the conservation status of mottled petrels.     

Burrow densities and nest site preferences of petrels (Procellariidae) at the Prince Edwards Islands

Summary The nest-site preferences of six burrowing petrel species, Salvin's prion Pachyptila vittata salvini, blue petrel Halobaena caerulea, great-winged petrel Pterodroma macroptera, Kerguelen petrel Pterodroma brevirostris, soft-plumaged petrel Pterodroma mollis and white-chinned petrel Procellaria aequinoctialis, in the northeastern part of Marion Island (Prince Edward Island group, southern Indian Ocean) were analyzed by step-wise multiple regression. The nest-site characteristics measured were slope angle, soil depth and moisture content, percentage cover by stones or boulders and percentage cover by each of seven major plant species. The major nest-site preferences were: exposed areas with shallow soil (Salvin's prion); steep coastal slopes (blue petrel); sheltered well-drained slopes with deep soil (great-winged petrels); wet areas along drainage lines (Kerguelen petrel); steep slopes (soft-plumaged petrel); and areas with deep soil (white-chinned petrel). Similar species showed no significant avoidance of nest sites where there were burrows of potential competitors but did tend to nest spread out over different habitats. Burrow densities were determined in six habitat and seven vegetation types. Salvin's prion was the most abundant species (81% of burrows, with a maximum density of 279 burrows ha^-1) and used both burrows and natural cavities for nesting. For all species combined, burrow densities at Marion Island were lower than in comparable habitats and vegetation types at neighbouring Prince Edward Island. Depredation by feral house cats Felis catus, absent from Prince Edward Island, is assumed to be largely responsible for this difference.     

Use of burrow entrance flaps to minimise interference to Chatham petrel (

The Chatham petrel (Pterodroma axillaris) is an endangered species, restricted to a single population on South East Island, Chatham Islands. The key threat to breeding success is loss of chicks as a result of interference by broad-billed prions (Pachyptila vittata) prospecting for burrows for their oncoming breeding season. The effectiveness in decreasing interference using an artificial burrow entrance flap was investigated. The flap exploits behavioural differences between the species. Chatham petrels have a high incentive to push through a flap due to their investment in their burrow and chick, while prospecting prions are influenced by ease of access when searching for potential burrows. This trial found 90% of Chatham petrels entered their burrows through the artificial flap. Flaps acted as barriers to broad-billed prions, where 22% entered the burrow through the flap (P <0.01) compared to the control burrows. Artificial burrow flaps have the potential to provide a low cost, low labour strategy for protecting the known breeding population of Chatham petrels.     

Determinants of between‐year burrow re‐occupation in a colony of the European bee‐eater Merops apiaster

Re‐occupation of existing nesting burrows in the European bee‐eater Merops apiaster has only rarely – and if so mostly anecdotically – been documented in the literature record, although such behavior would substantially save time and energy. In this study, we quantify burrow re‐occupation in a German colony over a period of eleven years and identify ecological variables determining reuse probability. Of 179 recorded broods, 54% took place in a reused burrow and the overall probability that one of 75 individually recognized burrows would be reused in a given subsequent year was estimated as 26.4%. This indicates that between‐year burrow reuse is a common behavior in the study colony which contrasts with findings from studies in other colonies. Furthermore, burrow re‐occupation probability declined highly significantly with increasing age of the breeding wall. Statistical separation of within‐ and between‐burrow effects of the age of the breeding wall revealed that a decline in re‐occupation probability with individual burrow age was responsible for this and not a selective disappearance of burrows with high re‐occupation probability over time. Limited duty cycles of individual burrows may be caused by accumulating detritus or decreasing stability with increasing burrow age. Alternatively, burrow fidelity may presuppose pair fidelity which may also explain the observed restricted burrow reuse duty cycles. A consequent next step would be to extend our within‐colony approach to other colonies and compare the ecological circumstances under which bee‐eaters reuse breeding burrows.     

First census of breeding seabirds between Cap Bienvenue (Terre Adélie) and Moyes Islands (King George V Land), Antarctica: new records for Antarctic seabird populations

Breeding population sizes of penguins, fulmarine etrels and skuas were estimated for the first time on a major part of the Terre Adélie coast and a section of the King George V Land coast during the 1997/1998 austral summer. We counted 106,400 breeding pairs and 12,400 Adélie penguin (Pygoscelis adeliae) chicks by direct counts, and 6960 breeding pairs from aerial photographs. Minimum breeding populations for other species are (direct counts): Antarctic fulmar (Fulmarus glacialoides) 6861 pairs, Antarctic petrel (Thalassoica antarctica) 4574 pairs, cape petrel (Daption capense) 194 pairs, snow petrel (Pagodroma nivea) 767 pairs, south polar skua (Catharacta maccormicki) 129 pairs and subantarctic skua (Catharacta lonnbergi) 1 breeding bird. We discovered 29 new seabird breeding locations in King George V Land, including 6 Antarctic fulmar, 4 Antarctic petrel, 3 cape petrel, 6 snow petrel and 10 south polar skua colonies. The largest colonies found contained up to 4205 breeding pairs of Antarctic fulmars. Population sizes of all species obtained in this study are higher than those found during previous partial surveys. Although these differences are in great part due to differences in survey methods, they also reflect real population changes. Our minimum population sizes obtained for a small portion of the Antarctic coast (<2%) suggest an underestimation of the estimated world breeding populations for several species of Antarctic seabirds. Accepted: 28 August 1998     

Model of burrow selection predicts pattern of burrow switching by Leach's Storm‐Petrels

Patterns of nest site selection exhibited at the scale of a population should result from initial preferences of individuals occupying nest sites as well as preferences exhibited by individuals moving between nest sites. We tested whether nest‐site preferences measured at the population scale were predictive of patterns of burrow switching by Leach's Storm‐Petrels (Oceanodroma leucorhoa), a long‐lived seabird that nests in underground burrows. Breeding pairs generally choose from the pool of available existing burrows rather than constructing new burrows, and a portion of the burrows in a colony remains unused in any breeding season. We quantified burrow preference at a colony on Kent Island, New Brunswick, over four breeding seasons. We used a classification and regression tree analysis to build a predictive model of nest‐site selection. Preferentially occupied burrows were drier, longer, had larger nest chambers, and were in areas of higher burrow density. To measure preferences during burrow switching, we tracked individuals that switched burrows, comparing characteristics of the burrows in which these birds were originally found to those they inhabited at the end of the study period. Characteristics preferred by switching individuals were a subset of those observed at the scale of the population; individuals moved to burrows that were drier, longer, and had larger nest chambers. Our results show how preferences of individuals that move between nest sites contribute to nest site preferences exhibited at the population scales commonly tested.     

COMPACT DISC REVIEW

ABSTRACT

In previous studies, calling sites of two species of burrowing frogs Eupsophus in southern Chile have been shown to amplify conspecific vocalizations generated externally, thus providing a means to enhance the reception of neighbour's vocalizations in breeding aggregations. In the current study the amplification of vocalizations of Eusophus roseus was investigated to explore the extent of sound enhancement reported previously for two congeneric species. Advertisement calls broadcast through a loudspeaker placed in the vicinity of a burrow, monitored with small microphones, are amplified by up to 14 dB inside cavities relative to outside. The fundamental resonant frequency of burrows, measured with broadcast noise and pure tones, ranges from 345–1335 Hz; however it is not correlated with burrow length. The spectra of incoming calls are altered inside burrows by predominantly increasing the amplitude of lower relative to higher harmonics. The call amplification effect inside burrows of E. roseus parallels the effect reported previously for two congeneric species and reinforces the suggestion that sound enhancement inside calling sites has a widespread effect on signal reception by burrowing animals.     

Burrow depth,carbon dioxide and reproductive success in Sand Martins Riparia riparia

Capsule: Carbon dioxide (CO₂) concentrations in the burrows of Sand Martins Riparia riparia increase with depth but have no detectable impact on fledging success.

Aims: To investigate whether burrow depth and CO₂ concentrations influence reproductive success in Sand Martins.

Methods: We monitored two Sand Martin colonies along the River Lune, Lancashire, UK, to investigate the effect of burrow depth on reproductive success. We also measured CO₂ levels in a sample of burrows to test whether burrow depth predicts CO₂ concentration, and to test for a relationship between CO₂ concentration and breeding success.

Results: Burrow depth was significantly correlated with fledging success, but the correlation was positive in first broods and negative in second broods. The highest CO₂ concentration recorded was 73?650?ppm and the mean concentration across burrows was 31?757?ppm. However, while CO₂ concentrations were positively correlated with burrow depth after controlling for the number and age of nestlings, they were not correlated with reproductive success.

Conclusion: There are reproductive costs associated with deeper burrows in second broods, but these could not be attributed to CO₂ concentrations despite the exceptionally high levels recorded. This study highlights the need for further investigation into gas exchange and the potential impacts of, or adaptations to, CO₂ accumulation in avian burrows.     

Monteiro's Storm‐petrel Oceanodroma monteiroi: a new species from the Azores

The existence of two seasonally distinct breeding populations of Oceanodroma storm‐petrels in the Azores islands was first documented in 1996. The discovery of morphological differences between the populations led to the suggestion that they may represent cryptic sibling species. Recent mtDNA and microsatellite analysis from storm‐petrel populations has considerably advanced our understanding of their taxonomic relationships. Here we present new information on the timing of breeding and moult of the two Azores populations, the extent of exchange of individuals between seasons, and diet from feather isotopes. We conclude that the hot‐season Azores population should be considered a new species for which we propose the name Oceanodroma monteiroi, Monteiro's Storm‐petrel. The species is both genetically distinct and genetically isolated from the sympatric cool‐season population of Madeiran Storm‐petrel Oceanodroma castro, and from all other populations of Oceanodroma castro in the Atlantic and Pacific Oceans examined to date. Differences in the vocalizations permit species recognition, and the extent of primary feather wear and stage of moult aids separation of the two species in the Azores, which is especially valuable during August when both attend the breeding colonies in large numbers. Feather carbon and nitrogen isotopes reveal that the diet of Monteiro's Storm‐petrel differs from that of the sympatric Madeiran Storm‐petrel during both breeding and non‐breeding seasons, and unlike the Madeiran Storm‐petrel, Monteiro's Storm‐petrel appears to maintain the same foraging environment during the summer and winter months, though it shows a dietary shift to higher trophic levels during the non‐breeding season. Monteiro's Storm‐petrel is thought to be confined to the Azores archipelago, where it is currently known to nest on just two small neighbouring islets. The total population size was estimated at 250–300 pairs in 1999.     

Estimating and Correcting for Bias in Population Assessments of Sooty Shearwaters

Abstract: We investigated the precision and accuracy of an infrared burrowscope for detecting sooty shearwater (Pufffinus griseus) chicks at 13 plots from 3 islands in southern New Zealand in 2003. We partially excavated burrows systems to reveal the entire burrow contents after 2 teams of observers had prospected all burrow entrances. Accuracy was similar between islands and observer teams at approximately 85%. The majority of the inaccuracy stemmed from failure to detect some chicks. Logistic regression modeling identified 4 burrow characteristics occurring between the entrance and the nest-site that influenced detection of burrow occupants. Detection was lower at nest-sites further from burrow entrances, in burrows with a high rate of burrow division, and in burrows with a high level of curvature. There was a positive relationship between the interaction of rate of division and curvature and detection of chicks. Distance from the burrow entrance was the only parameter that could be reliably used as a predictor of detection rate, so a reduced model containing only this variable was constructed to correct for burrowscope bias. The correction factor performed well on The Snares and Bench Island where predicted bias was very similar to observed levels (within 5%), but bias was overestimated on Putauhinu by up to 19.1%. Consistent bias, lack of damage to burrows from excavation, and the successful application of a correction factor all indicate the value of further testing burrowscope accuracy on other burrow-nesting seabird species.     

Olfactory navigation to the nesting burrow in Leach's petrel (oceanodroma leucorrhoa)

Visual, auditory, and olfactory navigation in the homing behaviour of Leach's petrel to the nesting burrow were investigated. Petrels returning to their burrows at night hovered above the thick spruce-fir canopy in the vicinity of the burrow before plummeting to the forest floor a few metres downwind of their burrows. They then walked upwind to their burrows. Birds landed closer to, and followed more circuitous routes to, their burrows in still air than in a wind. They failed to avoid obstacles in the path to burrows, often failed to locate accurately burrow entrances on first trial, and vocalized only after entering the burrow. In a Y-maze olfactorium, captive breeding petrels chose an air current coming from their own nest material in preference to one from similar materials collected on the forest floor. In the same apparatus, birds did not respond positively to air currents from their own stomach oil or preen gland oil. Petrels taken from burrows and released that same night did not return within a week if their external nares were plugged or if their olfactory nerves were transected. They did return if not operated on or if only subjected to sham operations. These results support an olfactory guidance system in burrow location and argue against visual or auditory guidance.     

Mitochondrial DNA analysis reveals genetic structure in two New Zealand Cook’s petrel (<Emphasis Type="Italic">Pterodroma cookii</Emphasis>) populations

The endangered Cook’s petrel (Pterodroma cookii) is restricted to two separated populations at the extremes of its former range across New Zealand. Prior work revealed morphological, foraging, and reproductive isolation between these two remnant populations. To aid the conservation management of the species, additional information is required on the genetic structure of Cook’s petrel. We used mitochondrial DNA sequences (Cytochrome Oxidase subunit 1 gene), collected from 26 and 19 Cook’s petrel breeding on Little Barrier Island (LBI) and Codfish Island (CDF), respectively, for this preliminary study. We uncovered distinct population genetic structure with analysis of molecular variance suggesting genetic isolation of the populations. Levels of genetic variation were higher in the LBI population (four haplotypes present; h = 0.34 and π = 0.10) whereas the CDF population had only one haplotype that was distinct from the LBI population. Our results indicate that Cook’s petrel constitute two distinct management units for which conservation of genetic as well as behavioural and morphological diversity should be a priority. Further genetic studies using nuclear markers are recommended.     

Obligate crayfish burrow use and core habitat requirements of crawfish frogs

Crawfish frogs (Lithobates areolatus) have experienced declines across large portions of their former range. These declines are out of proportion to syntopic wetland-breeding amphibian species, suggesting losses are resulting from unfavorable aspects of non-breeding upland habitat. Crawfish frogs get their common name from their affinity for crayfish burrows, although the strength of this relationship has never been formally assessed. We used radiotelemetry to address 4 questions related to upland burrow dwelling in crawfish frogs: 1) what burrow types are used and how do they function to affect crawfish frog survivorship; 2) what are the physical characteristics and habitat associations of crawfish frog burrows; 3) what are the home range sizes of crawfish frogs when burrow dwelling; and 4) where are crawfish frog burrows situated with respect to breeding wetlands? We tracked crawfish frogs to 34 burrows, discovered another 7 occupied burrows, and therefore report on 41 burrows. Crawfish frogs exclusively occupied crayfish burrows as primary burrows, which they inhabited for an average of 10.5 months of the year. With one exception, crawfish frogs also used crayfish burrows as secondary burrows—temporary retreats occupied while exhibiting breeding migrations or ranging forays. Burrows were exclusively located in grassland habitats, although crawfish frogs migrated through narrow woodlands and across gravel roads to reach distant grassland primary burrow sites. Home range estimates while inhabiting burrows were 0.05 m² (the area of the burrow entrance plus the associated feeding platform) or 0.01 m³ (the estimated volume of their burrow). Crawfish frog burrows were located at distances up to 1,020 m from their breeding wetlands. To protect crawfish frog populations, we recommend a buffer (core habitat plus terrestrial buffer) of at least 1.2 km around each breeding wetland. Within this buffer, at least 3 critical habitat elements must be present: 1) extensive grasslands maintained by prescribed burning and/or logging, 2) an adequate number of upland crayfish burrows, and 3) no soil disturbance of the sort that would destroy crayfish burrow integrity. © 2012 The Wildlife Society.     

Spatial Analysis of Effects of Mowing and Burning on Colony Expansion in Reintroduced Black‐Tailed Prairie Dog (Cynomys ludovicianus)

Factors governing the rate and direction of prairie dog (Cynomys spp.) colony expansion remain poorly understood. However, increased knowledge and ability to control these factors may lead to more effective reintroductions of prairie dogs and restoration of grassland habitats. We present density and directional analyses of the establishment of new burrows on three reintroduced colonies of Black‐tailed prairie dog (Cynomys ludovicianus) in southern New Mexico; the study colonies had been subjected to mow and burn treatments in the second year of the study. Our hypotheses were that prairie dogs will preferentially dig new burrows in the treatment plots versus control plots and that the colonies will expand in the direction of the treatment plots. The results support these hypotheses; analysis of burrow counts by site and treatment shows that prairie dogs preferentially colonized both mow and burn treatments compared to untreated areas at the periphery of the colonies. Directional analysis showed a significant posttreatment orientation of new burrows toward the treatment plots for all colonies. Our results show that the direction of expansion of prairie dog colonies can be manipulated. Effective control of the expansion of prairie dog colonies may lead to more successful reintroductions.     

Video camera count of burrow‐dwelling fairy prions,sooty shearwaters,and tuatara on Takapourewa (Stephens Island), New Zealand

Abstract

Video camera technology is an increasingly common tool in the study of burrow‐dwelling animals. A camera used to observe the inhabitants of narrow burrows on Takapourewa (Cook Strait, New Zealand) is described. Population densities (animals per m²) of up to 1.1 for fairy prions {Pachyptila turtur), 0.06 for sooty shearwaters (Puffinus griseus), and 0.15 for tuatara (Sphenodon punctatus) were estimated in four different habitats. These data are similar to other estimates collected in more labour intensive studies on the island, and provide baseline information for future conservation work on Takapourewa.