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Can small-scale predator control influence mallard duck (Anas platyrhynchos) nest survival? An experiment with artificial nests in Southland, New Zealand

Notornis, 69 (1), 45-53

C. Stewart; M. McDougall (2022)

Article Type: Paper

Artificial mallard (Anas platyrhynchos) nests were used to identify potential nest predators and assess whether small, farm-scale predator control could reduce mallard nest predation in Southland, New Zealand. Artificial nests were deployed over the mallard nesting period (late winter – spring) in both 2019 and 2020 and monitored with motion detection cameras. Prior to 2020 artificial nest deployment, farm-scale trapping of mammalian predators was conducted on one farm whilst the other was left as a control. Feral cats (Felis catus), brushtail possums (Trichosurus vulpecula), and European hedgehogs (Erinaceus europaeus) frequently visited the artificial nests but seldom preyed on them (i.e. consumed the eggs). Swamp harrier (Circus approximans) were the most common predator and were responsible for the destruction or predation of at least one egg at 17% of the artificial nests. Mammalian predator trapping had no noticeable effect on artificial nest predation, but did reduce the probability an artificial nest was visited by a cat, possum, or hedgehog. Results suggest typical predator control efforts of gamebird hunters does not reduce mallard nest predation, but may reduce nest disturbance and consequently mallard hen predation and nest abandonment.


Checklist 2022

Checklist of the birds of New Zealand. Fifth Edition. 2022, Occasional Publication (No. 1), 332 pp

OSNZ Checklist Committee (2022)

Article Type: Occasional Publication



Sexing of the endangered Floreana mockingbird (Mimus trifasciatus) using morphometric measurements

Notornis, 69 (4), 256-263

E.M.R. Reyes; A.N.H. Smith; D. Rueda; C. Sevilla; D.H. Brunton; L. Ortiz-Catedral (2022)

Article Type: Paper

Abstract: Male and female adult Floreana mockingbird (Mimus trifasciatus) have monomorphic plumage features that make them impossible to sex in the field. In this study, we use discriminant function analysis (DFA), a widely used technique, to assess the best measures to determine sex. We measured six morphological characteristics (mass, beak depth, beak width, tarsus length, wing length, and head-beak length) for birds of known sex (determined by molecular techniques) from the two extant populations of M. trifasciatus on Champion and Gardner islets, within the Galápagos archipelago. Using a coefficient of sexual dimorphism, we found that males are significantly larger than females in three of the variables. Discriminant functions using wing length and a combination of wing length + mass, and wing length + tarsus length could classify birds with a 98% level of accuracy. Furthermore, we were able to estimate a robust cut-off point to determine the sex of individuals in the field through a decision tree, using only wing length as morphological variable. Fast and accurate sexing of the bird based on one variable will reduce handling times and minimise stress for captured birds.














Post-translocation movements and ranging behaviour of roroa (great spotted kiwi, Apteryx maxima)

Notornis, 69 (3), 135-146

P. Jahn; J.G. Ross; V. Mander; L.E. Molles (2022)

Article Type: Paper

Translocations are increasingly used in kiwi (Apteryx spp.) conservation management, and their outcome is largely influenced by post-release dispersal and survival. A translocation of roroa (great spotted kiwi, A. maxima) to the Nina Valley, near Lake Summer Forest Park, is the first reintroduction of the Arthur’s Pass roroa population. In 2015, eight wild-caught adults were translocated from Arthur’s Pass National Park, following the release of ten captive-hatched subadults during 2011–13. We monitored the translocated kiwi by radio telemetry during 2015–17. Dispersal was highly variable among the released wild birds. The straight-line distance from the release site to the last recorded location ranged 0.5–10.3 km. Seven of the wild birds remained in the Nina Valley and covered an area up to 1,700 ha (95% utilisation distribution). Releasing the wild birds had no measurable impact on the ranging behaviour of previously released subadults. The current population founder group comprises a maximum of 13 unrelated individuals, and therefore further releases are necessary for a genetically viable population. Additionally, expansion of the pest-controlled area is crucial for the long-term persistence of the reintroduced population in the Nina Valley.