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Age and sex determination of Kakerori Pomarea dimidiata

Notornis, 40 (3), 179-187

H.A. Robertson; J.R. Hay; E.K. Saul (1993)

Article Type: paper

The Kakerori, or Rarotonga Flycatcher, of the Cook Islands has two distinctive colour forms: orange and grey. Our colour-band study showed that colour is simply related to age, not to sex as described earlier. When fledglings leave the nest their body is covered in grey down, and their wings and tail are still growing. Orange juvenal plumage is attained about one month after fledging. Despite having similar orange plumage, yearlings can be distinguished from 2 year-old birds on the basis of bill colour and wing and tail lengths. Third-year birds have elements of both main colour phases. Once the definitive basic plumage is attained in the fourth year, the age of grey birds cannot be determined. Wing and tail lengths apparently increase at each successive moult until the definitive basic plumage is reached. Males are larger than females, with bill length being the best discriminator. The progressive colour change recorded here parallels that described for three of the four other species of Pomarea flycatcher in eastern Polynesia, but colour variation in the other species, and in some other monarch flycatchers in the Pacific, needs critical examination. The ability to distinguish three cohorts of Kakerori is useful in measuring annual variations in productivity, survivorship, and age structure of the population.


A survey of birds on the Kaikorai Estuary

Notornis, 40 (4), 273-284

M.A. Miller (1993)

Article Type: paper

Monthly bird counts were recorded for Kaikorai Estuary, Otago from July 1989 to June 1991. Fifty species were noted, including passerines on the estuarine fringe. The predominant species was the Southern Black-backed Gull (Larus dominicanus), which accounted for 61% of the birds surveyed. They overwhelmed the Dunedin City Council refuse up site at Green Island and, to a lesser extent, a tip in private use. Mallards (Anas platyrhynchos) and Starlings (Sternus vulgaris) were the next most common species. Numbers of birds decreased with distance from the tip sites but, conversely, the number of species increased. Numbers were highest in March-April, but declined rapidly by two-thirds to a July-August low. This decline was due to the dramatic fall in duck numbers with the opening of duckshooting season and to the onset of winter. The total annual count for the second half of the survey (July 1990 to July 1991) was 4% down on the previous 12 months, but this was not statistically significant.






Decline of the Stewart Island population of the New Zealand Dotterel

Notornis, 40 (1), 1-13

J.E. Dowding; E.C. Murphy (1993)

Article Type: paper

Between 1988 and 1992, we conducted the first comprehensive survey of the number and breeding distribution of the New Zealand Dotterel (Charadrius obscurus) on Stewart Island. The population forms three post- breeding flocks, two of them on Stewart Island; band sightings have confirmed an earlier suggestion that the flock at Awarua Bay, Southland, is also composed of birds from the island. The population is widely spread over difficult terrain during the breeding season; autumn counts of the flocks provide the only practical means of assessing population size. Comparisons with earlier counts show that the population has declined to about one-fifth of its former size in the past 37 years The population is critically endangered because the decline continues and only 60-65 dotterels remain. Average annual mortality of banded adults between 1990 and 1992 was 23%. The major reason for the decline is believed to be predation by feral cats. Band sightings suggest that, apart from Southland, most or all of the recent NZ Dotterel records from the South Island coast (including Farewell Spit) are of juveniles wandering from Stewart Island.


Changes in bird numbers in six Northland forests 1979 – 1993

Notornis, 40 (4), 285-293

R.J. Pierce; R. Atkinson; E. Smith (1993)

Article Type: paper

A survey of birds in six Northland forests in 1979 was repeated in 1993, primarily to test whether numbers of New Zealand Pigeon had changed significantly. Counts of Eastern Rosella, Grey Warbler, Fantail and Tui had changed little. Counts of New Zealand Pigeon and Silvereye were significantly lower in 1993 and those of New Zealand Pigeon are thought to reflect long- term changes in abundance. Kaka and Kokako were each recorded in only one forest in 1993 compared with four and three forests respectively in the first survey. Pied Tit and Myna had significantly higher counts in 1993 than in 1979.




Habitat use by Chatham Island Pigeons

Notornis, 40 (1), 45-54

P.E. Pearson; G.C. Climo (1993)

Article Type: paper

In October-November 1990, Chatham Island Pigeons (Hemiphaga novaeseelandiae chathamensis) in the Tuku a tamatea and Awatotara Valleys, Chatham Island, preferred plants characteristic of mixed broadleaf forest over plants typical of tarahinau forest. Mixed broadleaf forest is confined to gullies and valleys in the region. Browsing by cattle, sheep, pigs and possums is rapidly degenerating these forest remnants. Conservation of Chatham Island Pigeon depends on the protection of these remnants.





The correct identity of the Black-toed Petrel Procellaria melanopus Gmelin, 1789

Notornis, 40 (4), 263-269

D.G. Medway (1993)

Article Type: paper

The Black-toed Petrel of Latham, on which Gmelin founded his Procellaria melanopus, has not previously been satisfactorily identified. For many years earlier this century, melanopus Gmelin was widely used as the name for the Providence Petrel Pterodroma solandri. On the basis of available evidence it is reasonable to conclude that Latham’s Black-toed Petrel was in fact a specimen of the Mottled Petrel Pterodroma inexpectata, taken in the course of Cook’s third voyage at sea off the north-west coast of North America, probably in the Gulf of Alaska in May 1778.



Contents of Blue Duck faeces from the Tongariro River

Notornis, 40 (3), 205-212

M.D. Wakelin (1993)

Article Type: paper

Aquatic invertebrates were extracted and identified from seven Blue Duck faeces collected from the Tongariro River in December 1990. A total of 927 aquatic invertebrates representing 37 taxa was identified. Over all samples, 45% of the aquatic invertebrates extracted were Chironornidae (samples ranging from 19-76%), 28% Trichoptera (ranging 11-49%), and 16% Ephemeroptera (ranging 2-42%). The dominant chironomid was Eukiefferiella sp., although Cricotopus spp. were also relatively abundant in some samples. Cased caddisflies were the main Trichoptera in all samples, but no one taxon was consistently dominant. Plecoptera comprised 0-20% of invertebrates in the faeces. In most samples collected below Tree Trunk Gorge, chironomids comprised ~61% of individuals recorded in the faeces, whereas above the gorge they comprised ~40% in any sample. Overall, the diet of Blue Duck on the Tongariro River in December 1990 was variable in terms of the proportions of species and the number of invertebrates that were consumed. This has also been shown in studies of Blue Duck diet on other rivers.


Anatomy of the mandibles, tongue and alimentary tract of Kakapo, with some comparative information from Kea and Kaka

Notornis, 40 (1), 55-63

E.J. Kirk; R.G. Powlesland; S.C. Cork (1993)

Article Type: paper

Preserved material from two Kakapo (Strigops habroptilus), two Kea (Nestor notabilis) and two Kaka (Nestor meridionalis) was dissected. A fledgling Kakapo had short, stout mandibles, a wide, thick tongue and a thick pharyngeal pad. The lower mandible closed against both the rostra1 end of the hard palate and the underside of the free end of the tongue. The crop was well defined. In the fledgling and in the headless body of an adult Kakapo a fusiform proventriculus was followed immediately by an approximately spherical, uniformly muscular gizzard. There were five main intestinal loops and no evidence of a vitelline diverticulum or of caeca. In Kea and Kaka the upper mandible was longer, the tongue (especially in Kaka) was narrower and fimbriated, and the crop was similar to that of the Kakapo. The mandibles, tongue and palate of the Kakapo appear to be particularly well adapted for the grinding of fibrous plant tissues to extract soft portions and juices.