Relevant bibliographies by topics / Hooker's sea lion

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Academic literature on the topic 'Hooker's sea lion'

Author: Grafiati
Published: 4 June 2021
Last updated: 12 February 2022

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Journal articles on the topic "Hooker's sea lion"

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BEDDARD, FRANK E. "XV. On the Structure of Hooker's Sea-Lion (Arctocephalus hookeri)." Transactions of the Zoological Society of London 12, no. 10 (July 7, 2010): 369–80. http://dx.doi.org/10.1111/j.1096-3642.1890.tb00004.x.

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Roe, WD, PJ Duignan, L. Meynier, GW de Lisle, and DV Cousins. "Tuberculosis in a New Zealand (Hooker's) sea lion." New Zealand Veterinary Journal 54, no. 1 (February 2006): 51. http://dx.doi.org/10.1080/00480169.2006.36610.

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Woodley, Thomas H., and David M. Lavigne. "Potential effects of incidental mortalities on the Hooker's sea lion (Phocarctos hookeri) population." Aquatic Conservation: Marine and Freshwater Ecosystems 3, no. 2 (June 1993): 139–48. http://dx.doi.org/10.1002/aqc.3270030206.

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Hawke, D. J. "Observations of Hooker's sea lion,Phocarctos hookeri, at a hauling ground on Otago Peninsula, New Zealand." New Zealand Journal of Marine and Freshwater Research 20, no. 3 (September 1986): 333–37. http://dx.doi.org/10.1080/00288330.1986.9516154.

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BEENTJES, MICHAEL P. "Comparative terrestrial locomotion of the Hooker's sea lion (Phocarctos hookeri) and the New Zealand fur seal (Arctocephalus forsteri): evolutionary and ecological implications." Zoological Journal of the Linnean Society 98, no. 4 (April 1990): 307–25. http://dx.doi.org/10.1111/j.1096-3642.1990.tb01204.x.

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Robinson, S., L. Wynen, and S. Goldsworthy. "PREDATION BY A HOOKER'S SEA LION (PHOCARCTOS HOOKERI) ON A SMALL POPULATION OF FUR SEALS (ARCTOCEPHALUS SPP.) AT MACQUARIE ISLAND." Marine Mammal Science 15, no. 3 (July 1999): 888–93. http://dx.doi.org/10.1111/j.1748-7692.1999.tb00855.x.

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Slooten, Elisabeth, and Stephen M. Dawson. "Conservation of marine mammals in New Zealand." Pacific Conservation Biology 2, no. 1 (1995): 64. http://dx.doi.org/10.1071/pc950064.

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New Zealand has a diverse fauna of marine mammals, comprising 35 cetacean and six pinniped species. None of these is hunted within the 200 mile Exclusive Economic Zone, but several species are killed incidentally in coastal or deep-water fisheries. Particularly affected are Hector's Dolphin, Hooker's Sea Lion, and the New Zealand Fur Seal. Detailed information on the nature and magnitude of incidental catches is patchy at best, and inadequate to assess nationally the impact on any one species. Other species are known to be caught, but a quantitative assessment of how many are caught per year is impossible. The impact of whale watching on sperm whales has attracted more attention, and impacts of tourism on other marine mammals are just beginning to be studied. We critically review the nature and management of the potential threats facing New Zealand marine mammals, including bycatch, entanglement in plastic debris, chemical pollution, and tourism. We discuss research needs and management recommendations for each conservation problem in turn.
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McMahon, Clive R., Dave Holley, and Susan Robinson. "The diet of itinerant male Hooker's sea lions, Phocarctos hookeri, at sub-Antarctic Macquarie Island." Wildlife Research 26, no. 6 (1999): 839. http://dx.doi.org/10.1071/wr98079.

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Scats were collected from itinerant male Hooker's sea lions, Phocarctos hookeri, at Macquarie Island and the uneroded faunal remains used to assess the diet. Uneroded sagittal otoliths were used to identify teleost fish and to calculate fish size. Prey items included 14 taxa of teleost fish, cephalopods, gastropods, crustaceans and fur seals. Fish constituted the primary component of the diet. Prey species previously uncommon in the diet of seals and penguins around Macquarie Island were commonly eaten by Hooker's sea lions. The sub-Antarctic horse fish (Zanclorhynchus spinifer) and the Patagonian tooth fish (Dissostichus eleginoides) were the two most abundant species and occurred in 62.5% and 41.7% of all scats respectively. There were no age-specific and individual differences in the diet of sea lions. Seasonal variances in diet were absent. Small plastic fragments (diameter ∼1 mm) were found only in association with otoliths of Electrona subaspera. Some overlap was seen between the diet of itinerant male Hooker's sea lions and the commercial fisheries that currently operate around Macquarie Island.
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Collins, Catherine J., B. Louise Chilvers, Matthew Taylor, and Bruce C. Robertson. "Historical population size of the threatened New Zealand sea lion Phocarctos hookeri." Journal of Mammalogy 97, no. 2 (December 29, 2015): 436–43. http://dx.doi.org/10.1093/jmammal/gyv187.

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Abstract Marine mammal species were exploited worldwide during periods of commercial sealing in the 18th and 19th centuries. For many of these species, an estimate of the pre-exploitation abundance of the species is lacking, as historical catch records are generally scarce and inaccurate. Genetic estimates of long-term effective population size provide a means to estimate the pre-exploitation abundance. Here, we apply genetic methods to estimate the long-term effective population size of the subantarctic lineage of the New Zealand sea lion (NZ sea lion), Phocarctos hookeri . This species is predominantly restricted to the subantarctic islands, south of mainland New Zealand, following commercial sealing in the 19th century. Today, the population consists of ~9,880 animals and population growth is slow. Auckland Island breeding colonies of NZ sea lion are currently impacted by commercial trawl fisheries via regular sea lion deaths as bycatch. In order to estimate sustainable levels of bycatch, an estimate of the population’s carrying capacity ( K ) is required. We apply the genetically estimated long-term effective population size of NZ sea lions as a proxy for the estimated historical carrying capacity of the subantarctic population. The historical abundance of subantarctic NZ sea lions was significantly higher than the target values of K employed by the contemporary management. The current management strategy may allow unsustainable bycatch levels, thereby limiting the recovery of the NZ sea lion population toward historical carrying capacity.
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Chilvers, B. Louise, and Ian S. Wilkinson. "Philopatry and site fidelity of New Zealand sea lions (Phocarctos hookeri)." Wildlife Research 35, no. 5 (2008): 463. http://dx.doi.org/10.1071/wr07053.

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The New Zealand sea lion (NZ sea lion), Phocarctos hookeri, is New Zealand’s only endemic pinniped, and one of the worlds rarest otariids. It is classified as ‘Threatened’ based primarily on the low number of breeding sites and restricted distribution. In New Zealand, a species listed as ‘threatened’ is required to be managed to allow its recovery and removal from the list within 20 years. For NZ sea lions this is dependant on the establishment of new breeding areas. However, understanding the recolonisation processes for pinnipeds is still in its infancy with factors such as philopatry needing more research to understand individual dispersal and the recolonisation process. This paper presents the first quantitative investigation into the level of site fidelity and philopatry to breeding beaches in NZ sea lions. Data from resights of NZ sea lions marked as pups from the northern Auckland Island breeding area suggest that both site fidelity and philopatry are important characteristics of this species. Our results show that overall: (1) females have a higher resighting rate than males, particularly at natal sites; (2) female non-natal resightings are predominantly restricted to locations within the northern Auckland Island breeding area (an area of ~10 km2), whereas male resightings are more widely dispersed (up to 700 km to NZ mainland); and (3) philopatry occurs for both sexes, but is more predominant in females than males, with males displaying delay related to sexual and social maturity. The colonisation of new breeding habitats rarely occurs when philopatry is strong and population density is low, stable or declining such as seen for NZ sea lions. Therefore, this research indicates that management of NZ sea lions needs to minimise anthropogenic mortality and encourage population growth to maximise density at breeding sites and encourage females to disperse to establish new breeding areas.
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Dissertations / Theses on the topic "Hooker's sea lion"

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Childerhouse, Simon, and n/a. "Conservation biology of New Zealand sea lions (Phocarctos hookeri)." University of Otago. Department of Marine Science, 2008. http://adt.otago.ac.nz./public/adt-NZDU20080213.144055.

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New Zealand sea lion (Phocarctos hookeri) is a pinniped endemic to New Zealand and is among the rarest of sea lion species. New Zealand sea lions are incidentally caught in the trawl fishery for squid around the Auckland Islands, and a sea lion catch-limit or Fishing Related Mortality Limit (FRML) is used to manage this interaction. Since 2003 such limits have been calculated using an age-structured Bayesian population model. One problem with this approach is that several key demographic parameters have had to be assumed, or are based on very few data. Archaeological and other historical records demonstrate that New Zealand sea lions were substantially more widespread before the arrival of humans to New Zealand than they are today (Chapter 2 published as Childerhouse & Gales 1998). The present population size is clearly reduced, with subsistence and commercial hunting the most likely cause of historical changes in distribution and abundance. Campbell Island, the only significant breeding site outside the Auckland Islands, was thoroughly surveyed for New Zealand sea lions for the first time in 2003. An estimated 385 pups were born there, comprising 13% of the total pup production for the species for 2003 (Chapter 3 published as Childerhouse et al. 2005). This thesis provides the first robust estimates of several demographic parameters for New Zealand sea lions. These data were gained via the capture, tagging and ageing of 865 individual females, which had come ashore to pup between 1999 and 2001. This research was underpinned by the development of a novel and robust ageing technique for live New Zealand sea lions (Chapter 5 published as Childerhouse et al. 2004). Chapters 6, 7 and 8 used analyses of the age structure of these females, and of subsequent resightings of them, and of known-age females between 1998 and 2005, provided the first estimates of individual growth, mean reproductive rate (0.67, SE = 0.01), mean adult survival (0.81, SE = 0.04), and maximum age (28 years) for females. These data show that New Zealand sea lions are among the slowest growing, slowest reproducing, and longest lived sea lion species. Significant differences in the age structure of the two largest breeding colonies highlight flawed assumptions of the current management approach. The application of this new demographic information has the potential to significantly alter the existing management advice relating to the setting of FRMLs and the impact of the squid fishery on the New Zealand sea lion population. Taken alone, these results suggest a dim outlook for an already threatened species. In the context that pup production is in significant decline (e.g. 32% since 1998 Chilvers et al. 2007), the species� foraging environment is thought to be marginal (Costa & Gales 2000), and that resource competition may also be impacting on the population (Chapter 4 published as Childerhouse et al. 2001a), the picture darkens further. Taken as a whole, these data suggest that current management is insufficient to ensure population stasis, let alone meet the Government�s statutory goal of recovery.
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Samaranayaka, Ari, and n/a. "Environmental stochasticity and density dependence in animal population models." University of Otago. Department of Mathematics & Statistics, 2006. http://adt.otago.ac.nz./public/adt-NZDU20060907.114616.

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Biological management of populations plays an indispensable role in all areas of population biology. In deciding between possible management options, one of the most important pieces of information required by population managers is the likely population status under possible management actions. Population dynamic models are the basic tool used in deriving this information. These models elucidate the complex processes underlying the population dynamics, and address the possible consequences/merits of management actions. These models are needed to guide the population towards desired/chosen management goals, and therefore allow managers to make informed decisions between alternative management actions. The reliability that can be placed on inferences drawn from a model about the fate of a population is undoubtedly dependent on how realistically the model represents the dynamic process of the population. The realistic representation of population characteristics in models has proved to be somewhat of a thorn in the side of population biologists. This thesis focuses in particular on ways to represent environmental stochasticity and density dependence in population models. Various approaches that are used in building environmental stochasticity into population models are reviewed. The most common approach represents the environmental variation by changes to demographic parameters that are assumed to follow a simple statistical distribution. For this purpose, a distribution is often selected on the basis of expert opinion, previous practice, and convenience. This thesis assesses the effect of this subjective choice of distribution on the model predictions, and develops some objective criteria for that selection based on ecological and statistical acceptability. The more commonly used distributions are compared as to their suitability, and some recommendations are made. Density dependence is usually represented in population models by specifying one or more of the vital rates as a function of population density. For a number of reasons, a population-specific function cannot usually be selected based on data. The thesis develops some ecologically-motivated criteria for identifying possible function(s) that could be used for a given population by matching functional properties to population characteristics when they are known. It also identifies a series of properties that should be present in a general function which could be suitable for modelling a population when relevant population characteristics are unknown. The suitability of functions that are commonly chosen for such purposes is assessed on this basis. I also evaluate the effect of the choice of a function on the resulting population trajectories. The case where the density dependence of one demographic rate is influenced by the density dependence of another is considered in some detail, as in some situations it can be modelled with little information in a relatively function-insensitive way. The findings of this research will help in embedding characteristics of animal populations into population dynamics models more realistically. Even though the findings are presented in the context of slow-growing long-lived animal populations, they are more generally applicable in all areas of biological management.
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Meynier, Laureline. "Feeding ecology of the New Zealand sea lion (Phocarctos hookeri) : a thesis presented in partial fulfilment of the requirements for the degree of Doctor Philosophy in Zoology at Massey University, Palmerston North, New Zealand." Massey University, 2009. http://hdl.handle.net/10179/901.

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The New Zealand (NZ) sea lion Phocarctos hookeri is the only pinniped endemic to NZ with a population of approximately 12,000 individuals. Its breeding range is currently restricted to NZ sub-Antarctic islands, and it has failed to recolonise its pristine distribution around the NZ main islands despite its protection since 1881. The current hypothesis is that the population growth of this pinniped is limited by the distribution of suitable prey on the Auckland Islands (50°30'S, 166°E) shelf, and by the direct and indirect pressure exerted by the arrow squid Nototodarus sloani fishery. However, this hypothesis has not been fully tested to date as there has been limited information on the diet of the NZ sea lion and their potential prey. The objective of this thesis is to analyse the diet of NZ sea lions over several years with particular emphasis on the most reproductively important segment of the population: lactating females. This thesis provides the first quantification by percentage mass of the diet of NZ sea lion using a combination of stomach content analysis, qualitative fatty acid (FA) analysis, and quantitative FA signature analysis (QFASA). Stomach contents and blubber FAs were analysed from 121 individuals incidentally caught (by-caught) in the southern arrow squid fishery from the years 1997 to 2006. The blubber FAs of 78 freeranging lactating females captured at Enderby Island, Auckland Islands, were also examined during January and February of 2000 to 2005. Data obtained from both stomach analysis and QFASA indicate that arrow squid, rattails Macrouridae, hoki Macruronus novaezelandiae and red cod Pseudophycis bachus are key prey species for NZ sea lions in the Auckland Islands region. Because these prey species live mostly at depths greater than 200 m, lactating females must undertake long foraging trips and dive regularly to greater depths than other sea lion species. Data from QFASA indicates that this foraging pattern is conducted over an extended period through the summer and autumn. The daily food requirement of a lactating female was estimated by a simple energetic model to be greater than 20% of its body mass. During years of low arrow squid recruitment such as 1999 and 2001, the amounts of squid required by the NZ sea lion population may have been similar to the amount harvested by the fishery, suggesting that resource competition is likely to occur between the arrow squid fishery and NZ sea lions in years of low squid abundance. Half of the fishing activity of the southern squid fishery occurs in the north of the Auckland Islands shelf where NZ sea lions forage, leading to incidental captures every year. This research emphasises that management of the NZ sea lion must not only consider the direct interactions with the arrow squid fishery, but also the likelihood of food resource competition between the fishery and NZ sea lions.
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Donaldson, Laura Patricia Constance. "The distribution of fatty acids and presence of environmental contaminants in the blubber of the New Zealand sea lion (Phocarctos hookeri) : a thesis presented in partial fulfilment of the requirements for the degree of Master of Science in Conservation Biology at Massey University, Palmerston North, New Zealand." Massey University, 2008. http://hdl.handle.net/10179/887.

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The conservation of marine mammals relies on the knowledge of species ecology in order to assess the impacts of anthropogenic activites and make appropriate species management decisions. Blubber biopsies are a relatively non-invasive sampling protocol to provide ecological information; two particular uses are for dietary analysis via fatty acid signature analysis (FASA) and investigating the uptake of organochlorine (OC) and polychlorinated biphenyl (PCB) environmental contaminants. Blubber composition and structure may vary according to body site and depth due to its dynamic functioning. This may result in the vertical stratification and heterogenous distribution of blubber FAs, OCs and PCBs between body sites, giving variable interpretations of diet and contaminant levels depending on biopsy sample site and depth. The aim of this thesis is to determine the FA distribution of blubber from two body sample sites (dorsal pelvic and ventral thoracic) currently used for FASA of the New Zealand sea lion, Phocarctos hookeri (NZSL) and to determine the level of OCs and PCBs in the blubber of healthy NZSLs for comparison to diseased NZSLs recorded in the 1997/98 epidemic. Blubber samples were collected from 29 by-caught NZSLs incidentally captured by the squid fishery around the Auckland Islands (50º42’S, 166º5’E) during the years 2005 to 2007 (not all NZSLs were able to be analysed for each chapter). Full blubber cores from both sample sites were collected from 18 NZSLs. Both sites showed a relative homogeneity of FA profiles, indicating the similar deposition and mobilisation of FAs at the two sample sites. To determine if FA stratification occurred, full blubber cores from both sample sites of 20 NZSLs were divided into inner and outer halves. Both sites displayed the same pattern of vertical stratification or biochemical layering of FAs between the two divisions, indicating that stratification of FAs occurs in the blubber of the NZSL. A range of OCs and PCBs were then determined in full thoracic blubber cores of seven NZSLs. The levels were higher than those previously recorded in NZSLs affected by disease during a 1997/98 epidemic. The SPCB in NZSLs was 0.034-0.192 mg/kg lipids, below the suggested threshold of 17 mg/kg for adverse health affects in marine mammals. From the results of this study I can support current blubber biopsy sampling techniques for FASA in NZSL. Obtaining full blubber cores from either the thoracic or pelvic sample site will give a comparable interpretation of diet. The low levels of blubber OCs and PCBs suggest a minor role of contaminants acting as a possible causative agent toward disease outbreaks in the NZSL. This research provides important information for developing correct and consistent blubber sampling techniques for NZSL and other pinniped species. This will ensure more accurate interpretations of ecological information obtained from blubber biopsies and therefore improved species management and conservation decisions that may be based on such research.
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Conference papers on the topic "Hooker's sea lion"

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Breen, P. A., and S. W. Kim. "An integrated Bayesian evaluation of Hooker's sea lion bycatch limits." In Sea Lions of the World. Alaska Sea Grant, University of Alaska Fairbanks, 2006. http://dx.doi.org/10.4027/slw.2006.30.

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Campbell, R. A., B. L. Chilvers, S. Childerhouse, and N. J. Gales. "Conservation management issues and status of the New Zealand (Phocarctos hookeri) and Australian (Neophoca cinerea) sea lion." In Sea Lions of the World. Alaska Sea Grant, University of Alaska Fairbanks, 2006. http://dx.doi.org/10.4027/slw.2006.29.

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