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Nearshore sightings of seabirds off the coast of Otago and Canterbury, New Zealand

Notornis, 71 (1), 1-11

S.D. Bourke; S. Bennington (2024)

Article Type: Paper

Abstract: Coastal and nearshore habitats are important to all seabird species. Understanding the distribution of seabirds in these environments can aid in their conservation. Despite the importance of coastal habitat, data collection for seabird species at sea is often difficult and resource intensive. Here, we take advantage of an established marine mammal surveying programme to collect distribution data for seabird species encountered in nearshore habitat. We surveyed seabird communities over 76 days in four locations along the southeast coast of New Zealand’s South Island; Dunedin, Moeraki, Timaru, and Banks Peninsula. We present observations of seabird species presence in these locations, as well as, a brief assessment of the counting techniques used during the study. In addition, we summarise the seabird numbers in relation to the marine mammal surveys (i.e. the presence and absence of dolphins). We aim to show the value of opportunistic data collection, while contributing to baseline species distribution knowledge.


Amendments to the 5th edition (2022) of the Checklist of the Birds of New Zealand

Notornis, 71 (3), 93-114

C.M. Miskelly; N.J. Forsdick; R.L. Palma; N.J. Rawlence; A.J.D. Tennyson (2024)

Article Type: Paper


Since the publication of the fifth edition of the Checklist of the Birds of New Zealand in 2022, 3 new vagrant species (2 terns and a storm petrel) have been accepted as occurring in New Zealand as at 31 December 2023, and 11 species that became extinct more than c. 1 million years ago have been described. These comprised 3 waterfowl, 1 owlet-nightjar, 1 tropicbird, 3 penguins, 1 albatross, 1 petrel, and a ‘false-colie’ (the latter is considered unrelated to any known group of birds). These 11 new fossil species were found in deposits of the following epochs: Paleocene (3), Miocene (6), and Pliocene (2). The richest areas for discovering new species were Miocene lacustrine deposits of the St Bathans region of Central Otago (5 species), and Paleocene marine deposits from the eastern South Island (3 species). Two Pliocene seabirds were from marine sediments in south Taranaki, and a Miocene albatross was found in a limestone quarry in South Canterbury. Recent publications potentially affecting the taxonomy, nomenclature, classification and arrangement of New Zealand birds are assessed, and recommendations are made that affect 56 taxa. This includes splitting Tibetan sand plover Anarhynchus atrifrons from Siberian sand plover A. mongolus, and Pyramid prion Pachyptila pyramidalis from fulmar prion P. crassirostris, thereby adding a further two species to the New Zealand bird list. The total number of bird species, including fossil species, now accepted from the New Zealand region is 502.


Primary moult of wrybills | ngutu pare (Anarhynchus frontalis)

Notornis, 71 (2), 46-56

T. Scott; A.C. Riegen; L.G. Underhill (2024)

Article Type: Paper

The wrybill | ngutu pare (Anarhynchus frontalis) is a small plover endemic to New Zealand with a unique laterally curved bill. Apart from moult, much of its biology is well understood: adults breed from late August to January on the braided river systems in Canterbury and inland Otago on New Zealand’s South Island. From midsummer, late December and January, they migrate north to non-breeding areas in the northern part of the North Island, especially to the large tidal bays, east and west of Auckland, where they undergo primary moult from January to April. The Underhill- Zucchini moult model was used to estimate the mean start and completion dates of primary moult, which were 20 January and 3 April respectively. Adults thus commence primary moult soon after arrival on non-breeding grounds but complete moult around four months before southward migration to their breeding areas in August. They appear to avoid primary moult during winter. Second-year birds start primary moult in December, one month earlier than the adults, but finish at approximately the same time. Primary moult of the wrybill is compared with closely related species, and with other waders that breed on the South Island and migrate to North Island for the non-breeding season.


Re-laying by Hutton’s shearwaters (Puffinus huttoni) at Te Rae o Atiu, Kaikōura Peninsula, New Zealand

Notornis, 71 (1), 12-22

L.K. Rowe; G. Taylor; T. Howard (2024)

Article Type: Paper

Abstract: Observations were made of the Nationally Vulnerable Hutton’s shearwater (Puffinus huttoni) breeding at Te Rae o Atiu, Kaikōura Peninsula (42.429°S, 173.703°E), New Zealand, a new colony established by translocations where birds breed in nestboxes. Over 12 seasons there were 245 eggs laid, including seven instances of two eggs laid as separate clutches in one nestbox during the same season. Nestbox inspections, usually undertaken weekly, provided evidence of egg laying date. Bird attendance at the nestboxes was also obtained from implanted passive integrated transponders that triggered a reader and datalogger. There is evidence for birds re-laying an egg after the first egg failed for three separate events, and a fourth was a possibility. In three other events, it appears more likely that two different birds laid the eggs, two as female-female pairings or simply egg dumping by an unpaired female; the third event was inconclusive. Only one of the 14 eggs from two-egg nests hatched, and the chick fledged successfully, about 10 days later than any other chick recorded at this colony. This fledging date was similar to the last date for fallout birds from the natural, mountain colonies, and suggests that re-laying may be a natural consequence of early egg failures in this species.














Corrigendum

Notornis, 71 (2), 67

R.N. Holdaway (2024)

Article Type: Correction

Holdaway, R.N.; Allentoft, M. E. 2022. A basic statistical approach to determining adult sex ratios of moa (Aves: Dinornithiformes) from sample series, with potential regional and depositional biases. Notornis 69: 158-173.