Academic literature on the topic 'Strigops habroptilus'

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Journal articles on the topic "Strigops habroptilus"

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Robertson, Bruce C., Craig D. Millar, Edward O. Minot, Don V. Merton, and David M. Lambert. "Sexing the Critically Endangered Kakapo Strigops habroptilus." Emu - Austral Ornithology 100, no. 4 (November 2000): 336–39. http://dx.doi.org/10.1071/mu00056.

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Alley, MR, BD Gartrell, HJ Mack, and CM McInnes. "Erysipelothrix rhusiopathiaesepticaemia in translocated kakapo (Strigops habroptilus)." New Zealand Veterinary Journal 53, no. 1 (February 2005): 94. http://dx.doi.org/10.1080/00480169.2005.36481.

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Gartrell, B. D., M. R. Alley, H. Mack, J. Donald, K. McInnes, and P. Jansen. "Erysipelas in the critically endangered kakapo (Strigops habroptilus)." Avian Pathology 34, no. 5 (October 2005): 383–87. http://dx.doi.org/10.1080/03079450500268583.

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TRIGGS, SUSAN J., RALPH G. POWLESLAND, and CHARLES H. DAUGHERTY. "Genetic Variation and Conservation of Kakapo (Strigops habroptilus: Psittaciformes)." Conservation Biology 3, no. 1 (March 1989): 92–96. http://dx.doi.org/10.1111/j.1523-1739.1989.tb00232.x.

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Haast, Julius. "Notes on the Ground-Parrot of New Zealand (Strigops habroptilus)." Ibis 6, no. 3 (June 28, 2008): 340–46. http://dx.doi.org/10.1111/j.1474-919x.1864.tb07874.x.

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Robertson, Bruce C., Edward O. Minot, and David M. Lambert. "Molecular sexing of individual kakapo, Strigops habroptilus Aves, from faeces." Molecular Ecology 8, no. 8 (August 1999): 1349–50. http://dx.doi.org/10.1046/j.1365-294x.1999.00692_2.x.

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Gartrell, BD, LS Argilla, J. Chatterton, S. Dennison-Gibby, A. Digby, J. Fulton, S. Hunter, KL Johnson, M. Jolly, and B. Lenting. "Surgical repair of a meningoencephalocoele in a kākāpō (Strigops habroptilus)." New Zealand Veterinary Journal 69, no. 4 (April 28, 2021): 247–54. http://dx.doi.org/10.1080/00480169.2021.1909509.

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Low, Matthew, Daryl Eason, and Kate McInnes. "Evaluation of passive integrated transponders for identification of Kakapo, Strigops habroptilus." Emu - Austral Ornithology 105, no. 1 (March 2005): 33–38. http://dx.doi.org/10.1071/mu04060.

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Merton, Don V., Rodney B. Morris, and Ian A. E. Atkinson. "Lek behaviour in a parrot:the Kakapo Strigops habroptilus of New Zealand." Ibis 126, no. 3 (April 3, 2008): 277–83. http://dx.doi.org/10.1111/j.1474-919x.1984.tb00250.x.

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White, DJ, RJ Hall, R. Jakob-Hoff, J. Wang, B. Jackson, and DM Tompkins. "Exudative cloacitis in the kakapo(Strigops habroptilus)potentially linked toEscherichia coliinfection." New Zealand Veterinary Journal 63, no. 3 (March 31, 2015): 167–70. http://dx.doi.org/10.1080/00480169.2014.960905.

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Dissertations / Theses on the topic "Strigops habroptilus"

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Whitehead, Joanna K. "Breeding success of adult female kakapo (Strigops habroptilus) on Codfish Island (Whenua Hou) : correlations with foraging home ranges and habitat selection." Lincoln University, 2007. http://hdl.handle.net/10182/640.

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Kakapo (Strigops habroptilus) are a flightless, nocturnal parrot endemic to New Zealand. Thought to be extinct within their natural range, kakapo are currently listed as nationally critical. The current population of 86 individuals is managed by the Department of Conservation’s National Kakapo Team on two offshore islands in southern New Zealand, with all females of breeding age on Codfish Island (Whenua Hou). Kakapo only breed once every two to five years, coinciding with the mast fruiting of specific plant species. On Codfish Island, the proportion of adult female kakapo that breed in rimu (Dacrydium cupressinum) fruiting years is dependent on the quantity of fruit produced, with fewer females attempting to breed during low mast years. The purpose of this research is to investigate why only some adult female kakapo breed in low rimu fruiting years on Codfish Island, specifically assessing if foraging home range size and/or habitat selection influence breeding. A total of 506 location points were collected at night for 18 adult female kakapo between March and May 2006. These were used to estimate foraging home ranges and to assess if kakapo select for particular types of vegetation. Ecological Niche Factor Analysis was used to determine the relative importance of habitat variables in the distribution of female kakapo and to predict areas of suitable breeding habitat when rimu fruit is limited. The breeding success of individuals in 2005, a low rimu mast year, was used to identify if differences in home ranges or habitat selection occurred between breeding and non-breeding females. The large variation in foraging home range sizes recorded in this research was consistent with previous studies. Foraging home range sizes were on average twice the size for breeders than for non-breeders, suggesting that adult female kakapo may be limited in their ability to breed by the size of the area they occupy. Adult female kakapo did not randomly use vegetation on Codfish Island as some vegetation types were not used, while others were common inside foraging home ranges. Adult female kakapo utilise a broad niche and are capable of surviving in a wide range of habitats. However, breeding females were more specialised in their niche requirements than non-breeders, with breeders utilising areas with higher abundances of mature rimu trees. Females occurred in high elevation, flat areas of the island but this may have been because this is where appropriate vegetation types occurred. During low rimu mast years, breeding adult females were predicted to occupy habitat in high elevation, plateau areas with a high abundance of rimu. Areas identified as sub-optimal habitat for breeding included the coastal areas, the lower elevation area of the main valley and some ridgelines. The home ranges of all 10 breeding females contained some optimal habitat, while females who did not breed were more likely to be located in sub-optimal habitat. Although there were significant areas of optimal breeding habitat not occupied by adult female kakapo, other kakapo may have been present in these areas. To increase the proportion of females that breed in low rimu mast years, it may be necessary to remove sub-adult females or surplus adult males living in optimal breeding habitat from the island. Alternatively, females in sub-optimal breeding habitat could be fed supplementary foods or transferred to other islands where there is unoccupied suitable breeding habitat available.
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Joyce, Leigh, and n/a. "Movement patterns, home range and habitat selection by Kakapo (Strigops habroptilus, Gray 1845) following translocation to Pearl Island, southern New Zealand." University of Otago. Department of Botany, 2009. http://adt.otago.ac.nz./public/adt-NZDU20090409.135626.

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Understanding the relationship between organisms and their environment is particularly important for the conservation and management of endangered species. The kakapo (Strigops habroptilus, Gray 1845) is a critically endangered, lek breeding, flightless nocturnal parrot endemic to New Zealand. In April 1998, a total population of fifty-six kakapo was known to survive on offshore islands. Twenty-six kakapo, thirteen males and thirteen females, were temporarily transferred to Pearl Island (518 ha), southern Stewart Island, from April 1998 to April 1999. The translocation of kakapo to Pearl Island, and subsequent breeding season, provided an ideal experimental framework to study kakapo dispersal, movement patterns, home range development, habitat selection, and lek development during the non-breeding and breeding seasons. A total of 4425 radio locations were analysed for all twenty-six birds, with a mean error polygon of 0.03 ha and an estimated average radio telemetry error of 21.6 m. Various home range analysis techniques were used to estimate kakapo home range size and overlap including: minimum convex polygons (MCP), modified minimum convex polygons (MMCP), harmonic mean analysis, adaptive kernel methods and cluster analysis. Estimates of kakapo home range size differed significantly depending on the method used (ANOVA, general linear model: F₁₃, ₁₀₇₆ = 63.99, p < 0.0001) and the season (F₂, ₁₀₇₆ = 160.75, p < 0.0001). Breeding home range size was significantly larger than non-breeding range size (mean difference = 67.6 ha, t₂₅ = 15.27, p < 0.0001). Calculations from 100% MCP and 95% harmonic mean analysis resulted in larger estimates of home range size and overlap compared to other methods. Cluster and kernel analyses appeared to give the most accurate home range representation for kakapo. Core home range areas showed a greater degree of similarity between methods. Male and female mean annual home range size did not differ significantly, whereas males had significantly (p < 0.05) larger home ranges than females during the nonbreeding season. Minimum convex polygons and harmonic mean analysis suggested that there was no significant difference in the way in which males and females interacted with each other. Kernel and cluster analyses indicated that females would overlap a greater proportion of another bird�s home range than males would. Cluster analysis also indicated that a female would have more of her home range occupied by another bird than a male would. The fact that different methods produced different quantitative results is an important consideration when using home range analysis to make conservation management decisions. Researchers must determine which method is the most appropriate for a particular research objective, species, or study area. The application of geographical information systems, ERDAS image classification techniques and global positioning systems was an integral part of this study. A large-scale vegetation classification map of Pearl Island was produced in order to quantify habitat selection by kakapo. The unsupervised classification technique produced the least accurate vegetation map, with an accuracy measure of 17-23%, compared to 52% for the supervised classification. The highest accuracy was obtained using an integrated approach involving inductive classification and deductive mapping, resulting in a vegetation classification map which correctly classified 95% of vegetation samples. Thirty-seven ecotone classes were identified and a total ecotone length of approximately 124 km was detected. Resource selection ratios and resource selection functions were estimated using a combination of discrete, continuous and area-based habitat variables. Circular buffers around used and available point locations were generated to determine whether kakapo selectively use vegetation mosaics. The probability of selection increased with increasing species diversity in each 75-metre radius buffer. Kakapo selected habitat mosaics and vegetation types with higher species diversity and moderate to high abundance of mature rimu and yellow silver pine trees.
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