Mobile Menu Open Mobile Menu Close

Search by:







Antipodean wandering albatrosses (Diomedea antipodensis) colonising the Chatham Islands

Notornis, 55 (2), 89-95

C.M. Miskelly; N. McNally; R. Seymour; D. Gregory-Hunt; J. Lanauze (2008)

Article Type: Paper

Large albatrosses, subsequently identified as Antipodean wandering albatrosses (Diomedea antipodensis), began prospecting for nest sites inland from the south-western coast of Chatham Island about 1998. The 1st egg was laid about the end of Mar 2003. What is presumed to be the same female laid an egg nearby in Feb 2004 and 2005. Although the 2004 egg hatched, each of these 3 breeding attempts failed. A subadult male Antipodean wandering albatross was found in Waipaua Scenic Reserve on Pitt Island in May 2002, and what may have been the same bird was ashore at the same site in Jan 2004. An egg was found at this site in Apr 2004 and the resulting chick fledged in Jan 2005. What is presumed to have been a different pair was found with an egg on Mount Hakepa, Pitt I, in early Jan 2006; their egg hatched in Apr 2006, and the chick fledged about 7 Jan 2007. What is presumed to be the same pair also nested successfully at the Mount Hakepa site in 2008/2009, with the chick fledging on 6 Jan 2009. These 6 breeding attempts (3 successful) by perhaps 3 different pairs at widely spaced sites on the Chatham Islands are the 1st records of Antipodean wandering albatrosses breeding away from the Antipodes Is and Campbell I.



Hybridisation between mallard (Anas platyrhynchos) and grey duck (A. superciliosa) on Lord Howe Island and management options

Notornis, 55 (1), 1-7

J.P. Tracey; B.S. Lukins; C. Haselden (2008)

Article Type: Paper

Introduced mallards (Anas platyrhynchos) occur on many islands of the South Pacific, where they hybridise with the resident grey duck (A. superciliosa). In October 2007, we conducted systematic surveys of Lord Howe Island to estimate the abundance and distribution of grey ducks, mallards, and their hybrids. Hybrids were common in areas of high public use, particularly where there was mown or grazed grass. Phenotypic characteristics suggest that mallards are now dominant and have supplanted the native grey duck, with 81% of birds classified as mallard or mallard-like hybrids, 17% as intermediate hybrids and only 2% as grey duck-like hybrids. No pure grey duck were observed. These hybrids pose direct and indirect economic, social and environmental impacts to Lord Howe Island. A management program to remove mallards using trapping, shooting and opportunistic capture by hand was conducted in October 2007. Standardised indices of duck abundance before and after management indicates that the total population was reduced by 71.7%. Eradication of mallard and hybrids from Lord Howe Island is considered achievable with a program of education, monitoring, and continued control to prevent re-establishment.


Rediscovery of the New Zealand storm petrel (Pealeornis maoriana Mathews 1932): two sightings that revised our knowledge of storm petrels

Notornis, 55 (2), 77-83

B.M. Stephenson; R. Flood; B. Thomas; S. Saville (2008)

Article Type: Paper

A small black-and-white storm petrel seen off Whitianga, New Zealand, in Jan 2003 was tentatively identified as a New Zealand storm petrel (Pealeornis maoriana). A further sighting in the Hauraki Gulf in Nov 2003 of multiple birds identified as New Zealand storm petrels led to the realisation that the species was both extant and apparently locally common. Prior to these sightings this enigmatic seabird was known only from 3 specimens collected in the 1800s, and unreported since. This paper reviews these 2 sightings that constitute the rediscovery of an


Breeding of variable oystercatchers (Haematopus unicolor) at Kaikoura Peninsula, South Island, New Zealand

Notornis, 55 (3), 146-154

L. Rowe (2008)

Article Type: Paper

The nesting of variable oystercatchers (Haematopus unicolor) on the Kaikoura Peninsula was studied at 6 sites over 8 years. Only in 1 year were birds known to have laid eggs at all 6 sites and only at 2 sites was nesting observed every year. Loss of nests often resulted in re-nesting and at 1 site birds made 4 attempts in 1 season. Over the 8 years, 117 eggs were found in 53 nesting attempts between mid-Oct and late Jan. The average size of 114 eggs was 58.2 x 40.6 mm. Thirty of 53 nesting attempts were completed and averaged 2.4 eggs/clutch (range 1

The birds of Nauru

Notornis, 55 (1), 8-19

D.W. Buden (2008)

Article Type: Paper

Thirty-four species of birds are recorded from the isolated Pacific island of Nauru. Six are treated as hypothetical pending corroboration; 3 others are introductions. Eighteen of the 25 indigenous species are non-breeding visitors (mainly migrating seabirds and shorebirds). The 7 confirmed or probable resident breeders include only 2 land birds, the Micronesian pigeon (Ducula oceanica) and the endemic Nauru reed-warbler (Acrocephalus rehsei). The Australian pelican (Pelecanus conspicillatus) and white-winged tern (Chlidonias leucopterus) are reported as first records for Nauru. Hunting pressure and habitat degradation have contributed to reduced numbers of the Micronesian pigeon and the once abundant black noddy (Anous minutus), but the Nauru reed-warbler occurs commonly in degraded and modified habitats. Second-stage mining to recover phosphate deposits will likely reduce available habitat further for all resident breeding species, although land restoration is also planned. Bird band recoveries indicate that many seabirds, especially black noddies, reach Nauru thousands of kilometres from where they were fledged, but to what extent they are recruited into the local breeding population is unknown.


Population numbers of the Caspian tern (Sterna caspia) in New Zealand

Notornis, 55 (2), 84-88

M. Bell; B.D. Bell (2008)

Article Type: Paper

During 1971-75 and 1991-95, surveys of Caspian tern (Sterna caspia) colonies throughout New Zealand were carried out. The breeding population in 1971-75 was 1266 pairs, in 16 colonies, predominately in the northern North Is. In 1991-95, there were 1190 breeding pairs found in 17 mainly northern colonies, suggesting the population had been relatively stable over the 20-year period. As census methodology may under-record the breeding of isolated pairs, we included an estimate of the number of isolated pairs to give a total national population of 1300-1400 breeding pairs. This is less than 3% of the global population. Colony size and location showed some change between survey periods; 6 colonies disappeared and 8 new colonies were formed. Addition surveys in 2011-2015 are recommended to compare recent population trends.

Possible tool use by an Australian magpie (Gymnorhina tibicen)

Notornis, 54 (4), 116-117

J. McCormick (2007)

Article Type: short note

[First paragraph…] Members of the parvorder Corvida, including the Australian magpie Gymnorhina tibicen, have a relatively high level of innovative behaviour amongst birds (Timmermans et al. 2000; Lefebvre et al. 2004). An example of this behaviour is tool use in Corvus spp. (Hunt 1996; Caffrey 2000). Although Australian magpies (magpies hereafter) are known to manipulate objects in behaviour such as play (Pellis 1981ab; Kaplan 2004) they have not been reported to use tools. Here, I report a possible case of tool use by an adult magpie.


Wader (Charadriiformes) and royal spoonbill (Platalea regia) use of roosts in Whangarei Harbour and Ruakaka Estuary, Northland, 1973-2000

Notornis, 54 (2), 83-91

A.J. Beauchamp; G.R. Parrish (2007)

Article Type: Paper

Roost sites in Whangarei Harbour and Ruakaka Estuary were used regularly by 12 wader species and 6 other species were present occasionally between 1974 and 2000. Counts at 7 roost sites in Nov, Jun/Jul, and Mar showed that 4 species, eastern bar-tailed godwit (Limosa lapponica), lesser knot (Calidris canutus), pied stilt (Himantopus leucocephalus), and South Island pied oystercatcher (Haematopus ostralegus finschi) contributed 70-99% (median 94%) of the waders. Most of the common waders used several roosts at each tide, but numbers and species richness of resident and vagrant species were greatest along the southern margin of the harbour. Changes in roost structure and proximity to feeding areas, and differences in migration patterns affected counts at individual roosts and the overall totals of wading birds counted in the harbour and its environs.

Longevity of a whitehead (Mohoua albicilla) on Tiritiri Matangi Island

Notornis, 54 (4), 233-233

N. Leuschner; P. Brekke; T. Cope (2007)

Article Type: short note

[First paragraphs…] At c.0800 h on 6 Nov 2006, PB and TC caught a whitehead (Mohoua albicilla) while mist-netting on Tiritiri Matangi I, Hauraki Gulf, North I, New Zealand. The net was set in “Bush 1”, on the northwestern side of the island. The bird carried a metal band (B57955) and 2 (green, blue) faded, inter-twined wrap-around plastic bands: the band combination could have been either metal-GB or metal-BG. It was thought to be male because it had a bright white head (Gill & McLean 1986) and an enlarged cloacal area. The only whiteheads that had been banded recently on the island had all been processed by NL and received split colour bands. We therefore thought that this whitehead was from the original trans-located population which was transferred to Tiritiri Matangi I from Little Barrier I in 1989 and 1990, which would mean that it was at least 16 years old. age of 8 years 7 months for another Little Barrier I bird (Gill 1993).


Notes on New Zealand pipit (Anthus n. novaeseelandiae) home range, parental care, and the behaviour of dependent young

Notornis, 54 (1), 44-47

A.J. Beauchamp (2007)

Article Type: short note

[First paragraph…]New Zealand pipits (Anthus n. novaeseelandiae) were apparently common in the open landscapes of the last glacial period (Worthy & Holdaway 1996). Before humans arrived, there were no mammalian predators in New Zealand but the pipit was an important food of the New Zealand falcon (Falco novaeseelandiae) and the laughing owl (Sceloglaux albifacies) (Worthy & Holdaway 2002). New Zealand pipits would have been likely to increase as more open habitats developed during the 700 years since Polynesian settlement, because their close relatives on continents live with mammalian and avian predators (Sibley & Ahlquist 1990), and New Zealand pipits have an 8-month (Aug-Mar) breeding season during which multiple clutches of 1-4 are raised (Heather & Robertson 1996). Pipits did apparently initially increase in numbers during the phase of forest and scrub clearance following European settlement (Buller 1888, Guthrie-Smith 1927), but no recent studies have found pipits in high densities in any habitat (Beauchamp 1995). The factors that could be controlling pipit numbers include the deteriorating quality of open habitats (Lovegrove 1980), and high levels of predation by endemic avian and introduced mammalian predators (Wilkinson & Wilkinson 1952).