Forty breeding colonies of three petrel species were found on 35 of 71 islands surveyed in southern Fiordland, Fiordland National Park, New Zealand, in November and December 2017. Almost all islands in Chalky Inlet, Preservation Inlet, Cunaris Sound, Long Sound, and Isthmus Sound were surveyed. Sooty shearwater (Ardenna grisea) was the most widespread and abundant species, with an estimated 23,425 burrows on 25 islands. Broad-billed prions (Pachyptila vittata) were breeding on nine islands (9,940 burrows estimated), and mottled petrels (Pterodroma inexpectata) on five islands (1,240 burrows estimated). This is a 3-fold increase in the number of petrel colonies in Chalky and Preservation Inlets and associated waterways identified in published accounts, and the first estimate of the number of burrows on each island. Long-term survival of most of these colonies is dependent on ongoing control of stoats (Mustela erminea) on islands in these southern fjords. The persistence of remnant petrel colonies on small islands is probably due to stoats being infrequent invaders that are unable to persist when migratory petrels depart at the end of the breeding season.
The monitoring of animal populations is essential for reporting on the state of the environment, with birds often used as indicators of ecosystem health. Traditionally, bird monitoring has been done by field observers; however,there has been recent interest in use of automatic recording devices (ARDs) as an alternative. A monitoring programme managed by the New Zealand Department of Conservation (DOC), used observers and ARDs concurrently for three survey seasons, providing the opportunity to compare results in terms of effectiveness and efficiency. The difference in species-richness estimates from the two methods was small, with the observer method detecting slightly higher numbers of species in all habitat types. Detection probabilities for individual species, derived from occupancy analysis, were similar between methods, with a few exceptions: bellbird (Anthornis melanura), brown creeper (Mohoua novaeseelandiae), tūī (Prosthemadera novaeseelandiae), North/South Island robin (Petroica longipes/australis), and rifleman (Acanthisitta chloris). Bellbird and rifleman had a higher probability of being detected by ARDs, whilst the remainder were more likely to be detected by observers. Differences in detection probability may be due to identification confusion in the case of bellbird and tūī, and observer ability to detect and identify birds visually for brown creeper and North/South Island robin. The relationship between indices of abundance from the observer and ARD methods varied between species and habitat types. These inconsistencies suggested that the ARD results did not correlate closely with observed abundance, which may limit the ARD method to provision of confirmed presence data. Observer counts proved to be more time efficient given present levels of processing technology, mainly due to the longer processing time required for ARD recordings. However higher numbers of people were required for observer counts, which may be problematic when there is a shortage of appropriately skilled observers at the required time of year.
Variable oystercatcher chicks (Haematopus unicolor) were banded at the Kaikōura Peninsula between summer 1999–2000 and summer 2016–2017. Prior to colour banding, there were no reports of Kaikōura Peninsula oystercatchers being sighted at other locations. Since summer 2006–2007 colour banding sequences have been available and these unique identifiers enabled movements of individual juvenile and immature birds to be determined. Forty-two colour banded chicks fledged, and 25 of these have been sighted at 11 locations between Collingwood 215 km to the northwest, and the Avon-Heathcote Estuary near Christchurch, 145 km south. Twelve of the 25 birds sighted away have not been seen back at the Kaikōura Peninsula, the other 13 returned of which 4 travelled away for a second time and did not return. Seventeen birds were not seen away from the Kaikōura Peninsula but 7 with no sightings for periods over 7 months may been away and returned. Siblings often went to different locations. Of 9 pairs of same nest siblings, 1 pair stayed at the Kaikōura Peninsula, 1 pair went initially to Nelson and 1 pair to the Avon-Heathcote Estuary, and birds of the other 6 pairs went to different locations including staying at Kaikōura. Birds seen at Nelson were also seen at the Avon-Heathcote Estuary.
Variability of face and wing pattern and of leg and bill colour, and differences in bill and wing lengths, were assessed in Anas superciliosa (Anatidae) specimens from Pacific Islands, Australia, and New Zealand regional populations. The same 3 broad face patterns and 4 wing patterns were found in all populations. Frequency distributions of face patterns, but not wing patterns, differed significantly between populations. The most common face pattern in Australia was very rare in New Zealand and uncommon in Pacific Islands. A secondary face pattern in Pacific Islands and New Zealand was absent in Australia. Australian and New Zealand ducks did not share bill colour and pattern and no legs of New Zealand birds displayed yellow/orange hues common to 35% of Australian specimens. Bill and wing lengths of Pacific Islands specimens were significantly shorter than all others while wing lengths of male specimens from northern Australia were significantly shorter than those from southern Australia and New Zealand. These differences offer emphatic support for historic subspecific differentiation of Pacific Island specimens. Historic, but now discarded, taxonomic distinction between Australian and New Zealand populations based on phenotype could be reconsidered.
Australasian little grebe (Tachybaptus novaehollandiae) was detected at the Whangarei sewerage wetlands at Kioreroa Road, in September–October 1996, and since 2012 has attempted to breed. Between October 2015 and April 2017, a pair of grebes produced 4 fledglings from 5 nesting attempts. Adults fed chicks for 26–29 days by diving in open areas with swamp lily (Ottelia avalifolia). Fledglings began independent foraging between 19 and 26 days old. Fledglings were not seen at the site after reaching c. 55-days old. The young from late clutches left the natal site in March–April, 3 weeks after their parents were last detected there. The site was not used by any grebes in June and July.
Face, wing, bill, and leg characteristics of grey ducks (Anas. s. superciliosa), of captive-raised F1 and backcrossed grey duck x mallard (A. platyrhynchos) hybrids, and of wild “grey-like” and “mallard-like” ducks in New Zealand were evaluated to assist recognition of grey duck x mallard hybrids in the field. Face pattern was the single character best able to discriminate grey ducks from all others, most grey-like hybrids from all mallard-like hybrids, but not most F1 and backcrossed mallard hybrids from mallards. Upper wing pattern, and bill and leg colours assisted discrimination alongside face pattern but not so on their own. The extensive phenotypic variability now apparent within the combined grey duck – mallard population in New Zealand restricts consistent discrimination to 3 “taxa”: grey ducks, grey-like ducks (“grallard/greylard”), and mallard-like ducks (“New Zealand mallard”).
Data on the effects of aerial 1080 operations on non-target bird species in New Zealand are scarce and largely limited to short-term colour-banding or radio-tracking studies, or standardised call counts. During a 22-year study in Tongariro Forest, all 142 radio-tagged North Island brown kiwi (Apteryx mantelli) survived 4 landscape-scale (20,000 ha) aerial broadcast 1080 operations targeting brush-tailed possum (Trichosurus vulpecula) and rats (Rattus spp.). Furthermore, both kiwi chick survival to 6 months old and New Zealand fantail (Rhipidura fuliginosa) nesting success were significantly higher in the first 2 breeding seasons following the use of 1080 poison than in subsequent years of the 5-year cycle. We observed several episodes of ferret (Mustela furo) killing multiple adult kiwi, particularly in the last half of the 1080 cycle. Population modelling showed that a 5-year 1080 operation cycle resulted in population gains for 2 years, followed by declines in the remaining 3 years that largely negated these benefits. Our data thus support the shift to a 3-year 1080 operation cycle which will more likely result in this kiwi population growing at close to the 2% per year target set by the 2018–2028 Kiwi Recovery Plan.
Four New Zealand pipit nesting attempts were monitored in an urban wasteland field in Onerahi, Whangarei.A female laid two clutches in dense kikuyu (Pennisetum clandestinum) in October and December 2015 and fledged young from both clutches. Pipits were then absent from the site from February until late August 2016. The male reappeared and used the exact same home range, with a new female. This female laid two nests in the more open low gorse (Ulex europaeus) and aristea (Aristea ecklonii) cover in September and October 2016 but both nests were depredated at 3–5 and seven days after hatching, respectively. All three chicks, the female, and possibly the male were killed during the latter predation event. There were differences in adult behaviour throughout the breeding cycle. The female constructed the nest and undertook all the incubation. During the incubation period the male was only present at the nest site in the early morning and did not roost at the site each evening. The pair was present throughout the day after the chicks hatched. Pipits used more frequent calling rates when there was a perceived threat, and when that threat was near a nest.
Black-fronted terns (Chlidonias albostriatus) are globally endangered and are one of six endemic bird species that rely on New Zealand’s braided river ecosystems for breeding. Like other marsh tern species, black-fronted terns are predicted to have low breeding-site fidelity due to the instability of their breeding habitat, small colony sizes and high predation rates. We used breeding colony location data collected from nine South Island rivers for 3–12 years (2004–2015) to investigate the breeding-site fidelity in black-fronted terns. The distribution of breeding colony locations from seven of the nine rivers analysed were not significantly different to a simulated random distribution. The tendency of black-fronted terns to form breeding colonies near past breeding site compared to new sites was only significant for two of the nine rivers analysed. Overall, there was low breeding-site fidelity in black-fronted tern colonies from year to year across the rivers analysed.