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Rhys Philip Buckingham (MNZM) Member of the New Zealand Order of Merit, For Services to Ecology.David Edgar Crockett Companion of the Queen’s Service Order, For Public Services.

[First paragraph…]The Kermadec Group lies about 1000 km northeast of North Island at 29º 15’S, 178º 00’W in the New Zealand archipelago. Its few land birds are all species characteristic of New Zealand: for example, the tui Prosthemadera novaeseelandiae (Cheeseman 1891, Sorensen 1964). Only the red-crowned parakeet is distinguished from its New Zealand counterpart, and then only at the subspecific level as Cyanoramphus novaezelandiae cyanurus (Higgins 1999).

Common land-birds in a rural suburban garden, Wellington, New Zealand, were counted for 10 minutes twice an hour, twice a month for 2 years, from dawn to dusk. The birds’ behaviour sometimes changed or they entered or left the study area during the day; so there is no ideal time of day for counting birds.

Breeding of North Island robins was monitored at two sites in Pureora Forest Park, central North Island, during the 19961 97 and 1997/98 breeding seasons. A total of 146 nests was found. First clutches were laid in September-October (mean: 20 September) and last clutches in November-January (mean: 17 December). Pairs had time to rear three broods during the breeding season (September-March), although most reared only two. Nest materials and nest location are described: mean nest height was 5.3 m (range 1.0 – 13.6). Mean clutch size was 2.60 (clutches of 2 or 3). Monthly mean clutch size increased from September to November, then decreased. The breeding biology of the North Island subspecies of robin at Pureora was similar to that of the South Island robin at Kaikoura. Nesting success improved dramatically after brushtail possums were poisoned by aerially distributed 1080 (sodium monofluoroacetate) baits, because mammalian predators were also poisoned. Robins are easy to monitor, and predation is a common cause of nest failure, so the species is potentially a valuable indicator of predator activity.

Banded Dotterels (Charadrius bicinctus bicinctus) exhibit a variety of seasonal movement patterns ranging from sedentary behaviour, through migration within New Zealand, to trans-Tasman migration. From 1985 to 1990 the Ornithological Society of New Zealand (OSNZ) studied the regional patterns of movement of Banded Dotterels which had been colour-banded on the breeding grounds. Sight-recoveries indicated that most birds in inland regions of the southern half of the South Island migrated to Australia, but coastal breeding birds in the South Island were mostly sedentary. Inland birds north of Canterbury mostly moved within New Zealand, particularly to harbours in the North Island but with regionally specific patterns – Westland birds mainly to Farewell Spit, Marlborough birds to the northern North Island and Farewell Spit, southern North Island birds either locally or to the Auckland region, and most Hawkes Bay and Volcanic Plateau birds to Bay of Plenty and Auckland. Breeding habitat modified this pattern; coastal birds were mainly sedentary, whereas birds on nearby inland riverbeds were migratory. Migration patterns are discussed in terms of advantages and disadvantages of different wintering options.

The nesting activities and breeding success of Black Shags (Phalacrocorax carbo) near Lake Kohangatera, Wellington, were studied from 1993 to 1998. The colony was used during November-July by a mean of 67 birds per night, but in August-October numbers increased to a mean of 98 birds when fledglings were present. Courtship and nest- building began in March, and nesting continued until October-November when the last chicks fledged. Most clutches (85% of 185) were laid in April-May (early nests), the remainder being laid in June-September (late nests). The mean estimated laying date of early nests varied from 14 April in 1998 to 3 May in 1995, the overall mean (1993-98) being 24 April. During the day typically the male took two incubation stints, including the first, and the female one or two. The mean length of incubation stints by females was 3 h 46 min, over an hour longer than that of males. However, the mean time females and males were absent from the colony to forage, 2 h 39 mins and 2 h 21 mins respectively, did not differ significantly. Three types of changeovers seen during incubation are described, as are the activities of adults and chicks during nestling rearing. Fledglings took their first flights when 49-60 days old, but continued to be fed by their parents for 40 to 80 days afterwards, the oldest fledged young seen fed being about 140 days old. Of 185 breeding attempts during 1993-98, 83% were successful, the majority resulting in one or two fledglings per nest. Mean brood size at fledging varied with year, from 1.1 in 1997 to 1.7 in 1998. Overall, the mean brood size was 1.4 fledged young per nest, and 1.7 for successful attempts. Early clutches were more productive than late ones. We conclude that a pair of Black Shags would be unable to successfully rear two broods and complete their moult within a year, and that late nestings were replacement clutches.

I tested the ability of captive Black Stilt chicks (Himantopus novaezelandiae) to capture and consume common aquatic invertebrates. Waterboatmen (Sigara sp.), segmented worms (Oligochaeta), and larvae of a damselfly (Xanthocnemis zealandica), midge (Chironomus zealandicus), mayfly (Deleatidium spp.), and caddisfly (Aoteapsyche colonica) were captured and consumed quickly and easily by chicks of all ages (2 – 30 days). They were also consumed in the greatest numbers. In contrast, two aquatic snails (Physa acuta and Lymnaea tomentosa) and larvae of two cased caddisflies (Triplectides sp. and Hudsonema amabilis) were captured and consumed with difficulty and in low numbers by young chicks (

Knowledge of the abundance of White-flippered Penguins and on the distribution of penguins without attached instruments at sea in general is scarce. Sightings of individual penguins in the neritic waters of southern Banks Peninsula were recorded between November 1993 and March 1997 to document their near-shore distribution and changes in seasonal abundance. White-flippered Penguins were not evenly distributed but appeared to concentrate in several bays. Abundance in Akaroa Harbour, the largest bay in the study area, peaked in April and November after recorded lows in March and September (probably due to moult and incubation), respectively.