Seabird bycatch data collected between 1996 and 2016 in commercial fisheries within the New Zealand Exclusive Economic Zone (EEZ) were analysed to determine if male and female grey petrels (Procellaria cinerea) have different at-sea foraging distributions during the breeding season. Data collection includes the return of bycaught (killed) seabirds from commercial fishing vessels by government fisheries observers. A total of 408 bycaught breeding grey petrels with known sex (214 males, 194 females) were analysed for a locational and seasonal sex bias. Data were also examined to determine whether where carcasses were returned from sea, there were different proportions of males and females captured by different fishing methods: offshore bottom longlining, surface longlining, and offshore trawling. There was no significant difference in the totals of male and female grey petrels returned from fishing operations, but capture locations for the sexes varied widely. More males than females were caught in April, May, August, and September. July showed a reverse trend, while June was the only month with no difference in captures between sexes. More males than females were caught in offshore bottom longliners and trawlers, with the opposite for surface longliners. This study emphasises the importance of a large-scale approach to capture locations and season when analysing impacts of fisheries on seabird populations, and highlights different foraging areas according to sex during the breeding season. Spatial segregation has important management implications as changes in fisheries practice in foraging areas may affect the sex ratio of the grey petrel population.
We assessed the impact of interspecific interactions on the breeding success of the South Georgian diving petrel (Pelecanoides georgicus; SGDP), a Nationally Critical seabird species, by monitoring 20 burrows at Codfish Island (Whenua Hou), with remote cameras. Additionally, we tested the utility of remote cameras to study the breeding biology and activity patterns of the SGDP by pairing 5 remote cameras with RFID readers. We recorded 7 different species at SGDP burrow entrances. The common diving petrel (P. urinatrix) likely caused two monitored burrows to fail. These results suggest that remote cameras are useful tools to study such interactions. However, the cameras had extremely low SGDP detection rates (mean = 10.86%; se = 7.62%) when compared to RFID readers. These low detection rates may be explained by the small body size and the speed at which SGDPs enter/leave burrows. Therefore, remote cameras, or at least the model and setup we used, appear unsuitable to study breeding biology and activity patterns in this seabird species.
We report Records Appraisal Committee (RAC) decisions regarding Unusual Bird Reports received between 1 January 2015 and 31 December 2016. Among the 113 submissions accepted by the RAC were the first New Zealand records of northern fulmar (Fulmarus glacialis), Herald petrel (Pterodroma heraldica), red-footed booby (Sula sula), laughing gull (Larus atricilla) and magpie-lark (Grallina cyanoleuca), the first breeding records for Australian wood duck (Chenonetta jubata) and glossy ibis (Plegadis falcinellus), and the second accepted records of shy mollymawk (Thalassarche cauta cauta), great shearwater (Puffinus gravis) and Cape gannet (Morus capensis). Other notable records included a pair of white-winged black terns (Chlidonias leucopterus) breeding in the Mackenzie basin, and the first record of pukeko (Porphyrio melanotus) from the Snares Islands. In addition, notable influxes of brown booby (Sula leucogaster) and great frigatebird (Fregata minor) occurred during 2015-16.
Museum study-skins are an important though under-utilised resource for studying the biology of endangered birds. This study compares the bill and cere morphology of female and male kākāpō (Strigops habroptilus) from three provenances: 1) “historical wild-origin” museum specimens collected from the North and South islands of New Zealand over 100 years ago; 2) the “modern wild-origin”, predominantly ex-Stewart Island Kākāpō Recovery Programme (KRP) founder population; and 3) the “modern non-wild” descendants of the founder population raised and maintained under the conservation management of the KRP. Bill length and gape was found to be smaller in the historical wild-origin birds than in the two contemporary groups. In comparison, historical wild-origin male kākāpō had larger ceres than both contemporary groups. As bird bills can show rapid morphological adjustment to diet over generational time scales, we evaluate whether bill size differences measured could be due to differences in the nutritional environments experienced by the birds either across their life-times or over recent evolutionary time. We also discuss whether regional variation in sexual selection might account for the provenance related variation in cere size.
I recorded the calling behaviours of shining cuckoos (Chrysococcyx lucidus) from 1992 – 2015 on Kawau Island. The 3 most common calls, the upward crescendo “whistling call,” the downward slur “call-note,” and the “call-note” with “chatter” notes, were given from the arrival of adults in late August-early September until early January. After January only the call-note was heard. The upward whistling calls averaged 9.5 notes per calling bout (se = 0.18, n = 721). There was no significant difference in the number of whistling notes given with or without following notes. Single call-notes from lone cuckoos or groups of birds were restricted to specific sites on ridges. Calling was infrequently heard during evening twilight, and not heard during darkness. There was an increase in the number of cuckoo detections after 2009, and this corresponded with the appearance of communal behaviour and calling.