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Population size, breeding frequency and survival of Salvin’s albatrosses (Thalassarche salvini) at the Western Chain, The Snares, New Zealand

Notornis, 58 (2), 57-63

P.M. Sagar; M.R. Charteris; J.W.A. Carroll; R.P. Scofield (2011)

Article Type: Paper

We investigated the population size and annual survival of Salvin’s albatrosses (Thalassarche salvini) breeding at the Western Chain, The Snares, New Zealand. A count of breeding pairs during incubation resulted in totals of 1100-1200 breeding annually on Toru and Rima Islets in the 3 years 2008-2010; none was seen breeding on Tahi, Rua or Wha Islets. The majority of adults bred annually. Based on banding and recapture the annual survival probability of breeding birds was estimated to be 0.967 while that of known-age birds banded as chicks in Feb 1986 was estimated at 0.939. A bird banded as a chick on the Bounty Is in 1985 was found breeding on Toru Islet of the Western Chain in the 3 years 2008-2010. This is the first record of a banded Salvin’s albatross breeding away from its natal island.






Summer home range size and population density of great spotted kiwi (Apteryx haastii) in the North Branch of the Hurunui River, New Zealand

Notornis, 58 (1), 22-30

C. Keye; C. Roschak; J. Ross (2011)

Article Type: Paper

Home range size, travel distances, and population density of the great spotted kiwi (Apteryx haastii) were investigated in the North Branch of the Hurunui River. Radio tracking was conducted on 10 great spotted kiwi between Dec 2007 and Apr 2008. The estimated minimum home-range sizes were determined using the concave polygon method and ranged between 19.6 ha and 35.4 ha, with a mean of 29.3 ha (± 1.6 SEM). The observed nightly distances travelled per hour varied from 7 to 433 m (n = 569). Most estimates of travel distances (73%) were clustered in the classes from 0 – 150 m/hour, and distances over 200 m/hour were seldom achieved (only c. 7% of distances). The kiwi population in the Mainland Island site on the western North Branch of the Hurunui River was estimated to hold around 290 birds in total. Population density for the entire North Branch area was estimated to be 2 pairs/km² and when including subadults, 5 birds/km². Our estimate of home range size is larger but with more variation than found in other studies. Differences in population density estimates between our study and those in the Hurunui and Arthurs Pass district may be due to different objectives and methods.


Hybridisation by South Island pied oystercatcher (Haematopus finschi) and variable oystercatcher (H. unicolor) in Canterbury

Notornis, 57 (1), 27-32

T. Crocker; S. Petch; P. Sagar (2010)

Article Type: Paper

We document hybridisation between South I pied oystercatcher (Haematopus finschi) and variable oystercatcher (H. unicolor) in Canterbury from 1989 to 2005. From 2 observations of hybridisation between South I pied oystercatcher x variable oystercatcher when first discovered, the hybrid swarm has increased to around 17 pairs, including South I pied oystercatcher pairs, variable oystercatcher pairs, hybrid pairs, and mixed pairs. We present data on the birds and their offspring and speculate on possible causes and implications of hybridisation for conservation of the taxa.

Density and pair fidelity in a translocated population of North Island robin (Petroica longipes)

Notornis, 56 (4), 206-212

S. McGavin (2010)

Article Type: Paper

The North Island robin (Petroica longipes) was introduced to the Zealandia – Karori Sanctuary in 2001. The sanctuary is a mainland island (225 ha) in Wellington that is free from all mammalian predators except mice (Mus musculus), and enclosed by a predator-proof fence. During 2001 and 2002 a total of 76 robins were translocated from Kapiti I to the sanctuary. To assess changes in this population since its introduction, I surveyed and mapped territories of robins in a 37 ha section of the sanctuary in 2008. Density has continued to increase, from 0.7 robins/ha in 2003 to 2.5 robins/ha in 2008. This density is higher than other mainland sites. Of 46 adult robins seen within the study area at the start of the 2004-05 breeding season, at least 17 remained within the area in 2008, close to their 2004 territories. These included 4 robins from the original transfer. In all cases where both partners from 2004 were seen in the study area in 2008, the pair bond remained intact. My survey confirms continued increase in this introduced population and high pair fidelity.



A review of the origin, European discovery, and first descriptions of the red shining-parrot (Prosopeia t. tabuensis) on ‘Eua, Kingdom of Tonga

Notornis, 57 (3), 128-134

D.G. Medway (2010)

Article Type: Paper

Evidence from Cook’s voyages supports the late prehistoric human introduction of the red shining-parrot (Prosopeia tabuensis tabuensis) from Fiji into the Tongatapu group, Kingdom of Tonga. It appears that a wild population of red shining-parrots was established on ’Eua by the time of Cook’s visits to the Tongatapu group in the 1770s. Latham used specimens obtained at ’Eua in 1777 for the 1st published description of the species. However, the correct type locality of the taxon is Fiji. A red shining-parrot specimen used by Latham is in the Naturhistorisches Museum in Vienna. It is 1 of the few bird specimens that survive from Cook’s voyages.

The diet of New Zealand falcons (Falco novaeseelandiae) on the Auckland Islands, New Zealand

Notornis, 57 (1), 19-26

N.H.S. Hyde; T.H. Worthy (2010)

Article Type: Paper

Prey remains and regurgitated pellets of New Zealand falcons Falco novaeseelandiae, from Adams I in the Auckland Is, were collected to determine the diet of this species in the subantarctic part of their range. Dissection of pellets revealed 1588 bones from 215 individuals of 18 species of birds preyed upon. Feathers associated with the remains supported the bone identifications. Rangle stones were also collected. The presence of procellariiform seabirds in the diet of falcons suggests some nocturnal hunting. While the single most frequent prey species was the bellbird (Anthornis melanura), Antarctic prion (Pachyptila desolata) and subantarctic diving petrel (Pelecanoides urinatrix exsul) were also common. When measured by prey weight, endemic land birds such as Auckland I rail (Lewinia muelleri), Auckland I snipe (Coenocorypha aucklandica aucklandica), and Auckland I teal (Anas aucklandica) constituted a third of the prey. Like many island birds, these ground-dwelling species cannot co-exist with introduced mammalian predators, but survive despite predation by native falcons.

Foraging behaviour and success of Australian white ibis (Threskiornis molucca) in an urban environment

Notornis, 56 (4), 201-205

N.J. Murray; P.P. Shaw (2010)

Article Type: Paper

The foraging behaviour and success of Australian white ibis (Threskiornis molucca) was investigated in a range of natural and artificial urban habitats in Queensland, Australia. Observations were made in tidal mudflat, freshwater wetland, rural grassland, urban park and landfill habitats. Australian white ibis exhibited a range of foraging behaviours, including both visual (fossicking, jabbing and pecking) and non-visual foraging behaviours (probing). The most common non-foraging behaviour was walking, followed by prey handling, pause and alert. Fighting was observed only in landfill habitats. Australian white ibis were able to capture food items in all habitats, although foraging success at landfills was more than twice as high as the other habitats. Food items captured at landfills required significantly more time to handle before swallowing. The ability of ibis to capture food items in all habitats indicates that they are effective habitat generalists.


Footedness in North Island kākā (Nestor meridionalis septentrionalis)

Notornis, 56 (3), 139-143

S. McGavin (2010)

Article Type: Paper

North Island kākā (Nestor meridionalis septentrionalis) often hold food in either their left or right foot when feeding. I observed kākā at Zealandia – Karori Sanctuary in Wellington in order to determine whether kākā show laterality (specifically footedness) when holding food. Laterality was seen at the individual level, i.e. individual kākā tended to consistently use the right foot or consistently use the left foot to hold food. However, there was no significant population level laterality, i.e. a similar proportion of the kākā showed bias towards using the left foot as the right foot. The kākā I studied were banded with a wide band on 1 foot and 2 narrow bands on the other foot. There did appear to be a population level bias towards holding food in the foot banded with the single wide band, but the reason for this was unknown and further study is needed.