The Experts below are selected from a list of 93 Experts worldwide ranked by ideXlab platform
Bruce C. Robertson - One of the best experts on this subject based on the ideXlab platform.
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Historical population size of the threatened New Zealand sea lion Phocarctos hookeri
Journal of Mammalogy, 2015Co-Authors: Catherine J. Collins, B. Louise Chilvers, Matthew Taylor, Bruce C. RobertsonAbstract: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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sexual segregation in juvenile new zealand sea lion foraging ranges implications for intraspecific competition population dynamics and conservation
PLOS ONE, 2012Co-Authors: Elaine S Leung, Louise B Chilvers, Shinichi Nakagawa, Antoni Moore, Bruce C. RobertsonAbstract:Sexual segregation (sex differences in spatial organisation and resource use) is observed in a large range of taxa. Investigating causes for sexual segregation is vital for understanding population dynamics and has important conservation implications, as sex differences in foraging ecology may affect vulnerability to area-specific human activities. Although behavioural ecologists have proposed numerous hypotheses for this phenomenon, the underlying causes of sexual segregation are poorly understood. We examined the size-dimorphism and niche divergence hypotheses as potential explanations for sexual segregation in the New Zealand (NZ) sea lion (Phocarctos hookeri), a nationally critical, declining species impacted by trawl fisheries. We used satellite telemetry and linear mixed effects models to investigate sex differences in the foraging ranges of juvenile NZ sea lions. Male trip distances and durations were almost twice as long as female trips, with males foraging over the Auckland Island shelf and in further locations than females. Sex was the most important variable in trip distance, maximum distance travelled from study site, foraging cycle duration and percent time at sea whereas mass and age had small effects on these characteristics. Our findings support the predictions of the niche divergence hypothesis, which suggests that sexual segregation acts to decrease intraspecific resource competition. As a consequence of sexual segregation in foraging ranges, female foraging grounds had proportionally double the overlap with fisheries operations than males. This distribution exposes female juvenile NZ sea lions to a greater risk of resource competition and bycatch from fisheries than males, which can result in higher female mortality. Such sex-biased mortality could impact population dynamics, because female population decline can lead to decreased population fecundity. Thus, effective conservation and management strategies must take into account sex differences in foraging behaviour, as well as differential threat-risk to external impacts such as fisheries bycatch.
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the population decline of the new zealand sea lion phocarctos hookeri a review of possible causes
Mammal Review, 2011Co-Authors: Bruce C. Robertson, Louise B ChilversAbstract:The New Zealand (NZ) sea lion Phocarctos hookeri is NZ's only endemic pinniped and is listed as 'nationally critical'. The species breeds in the NZ sub-Antarctic: 71% of the population at the Auckland Islands (2010 pup production: 1814 39) and the remaining 29% on Campbell Island (726 pups in 2010). 2. Pup production at the Auckland Islands has declined by 40% since 1998 (1998: 3021 pups produced): only 1501 pups were born in 2009. This decline is directly linked to philopatric females not returning to breeding areas. While the Auckland Island population has declined, the Campbell Island population appears to be increasing slowly. 3. Potential reasons for the decline in the Auckland Island population, but not in the Campbell Island population, include non-anthropogenic factors: (i) disease epizoot- ics, (ii) predation, (iii) permanent dispersal or migration, (iv) environmental change; and anthropogenic impacts: (v) population 'overshoot', (vi) genetic effects, (vii) effects of contaminants, (viii) indirect effects of fisheries (i.e. resource competition) and (ix) direct effects of fisheries (i.e. by-catch deaths). Of the nine potential reasons examined here, six can be discounted (ii-vii). Bacterial epizootics (i) occur in the NZ sea lion population, but their impact has predominantly increased pup mortality, which is unlikely to cause the severe decline observed, as pup mortality throughout the species is naturally high and variable. 4. The most plausible hypotheses, based on available evidence, are that the observed decline, in particular, the decreasing number of breeding females in the Auckland Island population, is caused by (viii) fisheries-induced resource competition and (ix) fisheries-related by-catch. By-catch is the main known anthropogenic cause of mortality in the species. Competition with fisheries resulting in resource compe- tition, nutrient stress and decreased reproductive ability in NZ sea lions should be a priority area for future research.
Louise B Chilvers - One of the best experts on this subject based on the ideXlab platform.
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population viability analysis of new zealand sea lions Auckland Islands new zealand s sub antarctics assessing relative impacts and uncertainty
Polar Biology, 2012Co-Authors: Louise B ChilversAbstract:A common issue faced in wildlife management is how to assess the uncertainty of potential impacts on the viability of a species or population. The pup production of New Zealand (NZ) sea lions (Phocarctos hookeri) has declined 50% in the last 12 years at their main breeding area, the Auckland Islands. The two major known atypical impacts on NZ sea lions are as follows: (1) the direct mortality as bycatch of trawling and (2) bacterial epizootics, which can affect reproduction and mortality. Both of these impacts include high levels of uncertainty, with fisheries data being variable due to percentage observer coverage and the effect of sea lion exclusion devises, while the timing and severity of bacterial epizootics are not predictable. In this paper, an age-structured model of the NZ sea lion population at the Auckland Islands was built to examine the predicted effects of fisheries mortality and catastrophes (bacterial epizootics), both separately and then combined, on population viability over a 100-year period using the VORTEX population viability analysis programme. These models are then compared against 15 years of empirical field data to determine the actual level of impacts being observed. Model results indicate that although naturally occurring epizootics reduce the growth rate of the population, it does not cause a decline in the Auckland Island population. However, sustained fisheries bycatch at current estimated levels, particularly considering its potential impact on adult female survival, could result in a population decline and possible functional extinction over the modelled time period.
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sexual segregation in juvenile new zealand sea lion foraging ranges implications for intraspecific competition population dynamics and conservation
PLOS ONE, 2012Co-Authors: Elaine S Leung, Louise B Chilvers, Shinichi Nakagawa, Antoni Moore, Bruce C. RobertsonAbstract:Sexual segregation (sex differences in spatial organisation and resource use) is observed in a large range of taxa. Investigating causes for sexual segregation is vital for understanding population dynamics and has important conservation implications, as sex differences in foraging ecology may affect vulnerability to area-specific human activities. Although behavioural ecologists have proposed numerous hypotheses for this phenomenon, the underlying causes of sexual segregation are poorly understood. We examined the size-dimorphism and niche divergence hypotheses as potential explanations for sexual segregation in the New Zealand (NZ) sea lion (Phocarctos hookeri), a nationally critical, declining species impacted by trawl fisheries. We used satellite telemetry and linear mixed effects models to investigate sex differences in the foraging ranges of juvenile NZ sea lions. Male trip distances and durations were almost twice as long as female trips, with males foraging over the Auckland Island shelf and in further locations than females. Sex was the most important variable in trip distance, maximum distance travelled from study site, foraging cycle duration and percent time at sea whereas mass and age had small effects on these characteristics. Our findings support the predictions of the niche divergence hypothesis, which suggests that sexual segregation acts to decrease intraspecific resource competition. As a consequence of sexual segregation in foraging ranges, female foraging grounds had proportionally double the overlap with fisheries operations than males. This distribution exposes female juvenile NZ sea lions to a greater risk of resource competition and bycatch from fisheries than males, which can result in higher female mortality. Such sex-biased mortality could impact population dynamics, because female population decline can lead to decreased population fecundity. Thus, effective conservation and management strategies must take into account sex differences in foraging behaviour, as well as differential threat-risk to external impacts such as fisheries bycatch.
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the population decline of the new zealand sea lion phocarctos hookeri a review of possible causes
Mammal Review, 2011Co-Authors: Bruce C. Robertson, Louise B ChilversAbstract:The New Zealand (NZ) sea lion Phocarctos hookeri is NZ's only endemic pinniped and is listed as 'nationally critical'. The species breeds in the NZ sub-Antarctic: 71% of the population at the Auckland Islands (2010 pup production: 1814 39) and the remaining 29% on Campbell Island (726 pups in 2010). 2. Pup production at the Auckland Islands has declined by 40% since 1998 (1998: 3021 pups produced): only 1501 pups were born in 2009. This decline is directly linked to philopatric females not returning to breeding areas. While the Auckland Island population has declined, the Campbell Island population appears to be increasing slowly. 3. Potential reasons for the decline in the Auckland Island population, but not in the Campbell Island population, include non-anthropogenic factors: (i) disease epizoot- ics, (ii) predation, (iii) permanent dispersal or migration, (iv) environmental change; and anthropogenic impacts: (v) population 'overshoot', (vi) genetic effects, (vii) effects of contaminants, (viii) indirect effects of fisheries (i.e. resource competition) and (ix) direct effects of fisheries (i.e. by-catch deaths). Of the nine potential reasons examined here, six can be discounted (ii-vii). Bacterial epizootics (i) occur in the NZ sea lion population, but their impact has predominantly increased pup mortality, which is unlikely to cause the severe decline observed, as pup mortality throughout the species is naturally high and variable. 4. The most plausible hypotheses, based on available evidence, are that the observed decline, in particular, the decreasing number of breeding females in the Auckland Island population, is caused by (viii) fisheries-induced resource competition and (ix) fisheries-related by-catch. By-catch is the main known anthropogenic cause of mortality in the species. Competition with fisheries resulting in resource compe- tition, nutrient stress and decreased reproductive ability in NZ sea lions should be a priority area for future research.
Robert B. Elliott - One of the best experts on this subject based on the ideXlab platform.
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No PERV transmission during a clinical trial of pig islet cell transplantation
Virus research, 2016Co-Authors: Vladimir A. Morozov, Shaun Wynyard, Adrian Abalovich, Joachim Denner, Robert B. ElliottAbstract:Xenotransplantation of pig islet cells is a promising alternative for the treatment of diabetes with insulin and may help to prevent numerous late complications such as blindness and amputation. First encouraging results using porcine islets have been reported in preclinical animal models as well in the first clinical trial in New Zealand. The goal of this manuscript is to examine the biological safety of a second trial performed in Argentina, specifically in regards to the transmission of porcine endogenous retroviruses (PERVs) using improved detection methods As in the first trial encapsulated islet cells from the well-characterised Auckland Island pigs were used. The animals were not genetically modified. The islet cells were transplanted in eight human recipients using a modified clinical protocol. Sera taken at different time points after transplantation (up to 55 weeks) were screened for the presence of antibodies against PERV proteins by Western blot analysis using viral antigens from highly purified virus particles. Positive sera obtained by immunization with recombinant PERV proteins were used as control sera. In none of the patients antibodies against PERV were detected, indicating the absence of infection. In parallel at different time points (up to 113 weeks) white blood cells (WBC) have been tested for PERV DNA, and WBC and plasma for PERV RNA by real-time RT-PCR. All tests were negative. In addition, using primers detecting pig mitochondrial cytochrome oxidase (COX) gene, patients were screened for microchimerism. In summary, the data are further evidence for the safety of pig islet cell transplantation.
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microbiological safety of the first clinical pig islet xenotransplantation trial in new zealand
Xenotransplantation, 2014Co-Authors: Shaun Wynyard, Joachim Denner, Olga Garkavenko, Divya Nathu, Robert B. ElliottAbstract:Background Xenotransplantation using pig cells, tissues, or organs may be associated with the transmission of porcine microorganisms and the development of zoonoses. Among all porcine microorganisms porcine endogenous retroviruses (PERVs) represent a special risk because they are integrated in the genome of all pigs and able to infect human cells. In previous preclinical and retrospective clinical trials of xenotransplantation, no transmission of PERV was observed. The first clinical trial of (alginate-encapsulated) porcine islet cell transplantation in New Zealand, which was approved by the New Zealand Government as an open-label phase I/IIa safety/efficacy trial, offers the possibility to analyze microbiological safety in a prospective clinical study. Methods Before the trial started, a multilevel testing strategy was used to screen for 26 microorganisms in donor pigs of the Auckland Island strain and the islet cell preparations used for treatment. Donor testing was performed using molecular methods including multiplex real-time PCR. Blood samples from 14 pig islet cell recipients were also investigated by molecular biological methods at weeks 1, 4, 8, 12, 24, and 52 post-transplant for the transmission of porcine microorganisms. Sera were also monitored at these time points for antibodies against PERVs. Results Beginning in 2009, fourteen patients with severe unaware hypoglycemia were treated with one of four different dosages of alginate-encapsulated porcine islets ranging from 5000–20 000 islet equivalents delivered in a single dose. No transmission of either PERVs or other porcine microorganisms was detected by PCR and immunological methods. Conclusion These findings support previous results and strongly indicate the safety of xenotransplantation as performed here.
Shaun Wynyard - One of the best experts on this subject based on the ideXlab platform.
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No PERV transmission during a clinical trial of pig islet cell transplantation
Virus research, 2016Co-Authors: Vladimir A. Morozov, Shaun Wynyard, Adrian Abalovich, Joachim Denner, Robert B. ElliottAbstract:Xenotransplantation of pig islet cells is a promising alternative for the treatment of diabetes with insulin and may help to prevent numerous late complications such as blindness and amputation. First encouraging results using porcine islets have been reported in preclinical animal models as well in the first clinical trial in New Zealand. The goal of this manuscript is to examine the biological safety of a second trial performed in Argentina, specifically in regards to the transmission of porcine endogenous retroviruses (PERVs) using improved detection methods As in the first trial encapsulated islet cells from the well-characterised Auckland Island pigs were used. The animals were not genetically modified. The islet cells were transplanted in eight human recipients using a modified clinical protocol. Sera taken at different time points after transplantation (up to 55 weeks) were screened for the presence of antibodies against PERV proteins by Western blot analysis using viral antigens from highly purified virus particles. Positive sera obtained by immunization with recombinant PERV proteins were used as control sera. In none of the patients antibodies against PERV were detected, indicating the absence of infection. In parallel at different time points (up to 113 weeks) white blood cells (WBC) have been tested for PERV DNA, and WBC and plasma for PERV RNA by real-time RT-PCR. All tests were negative. In addition, using primers detecting pig mitochondrial cytochrome oxidase (COX) gene, patients were screened for microchimerism. In summary, the data are further evidence for the safety of pig islet cell transplantation.
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microbiological safety of the first clinical pig islet xenotransplantation trial in new zealand
Xenotransplantation, 2014Co-Authors: Shaun Wynyard, Joachim Denner, Olga Garkavenko, Divya Nathu, Robert B. ElliottAbstract:Background Xenotransplantation using pig cells, tissues, or organs may be associated with the transmission of porcine microorganisms and the development of zoonoses. Among all porcine microorganisms porcine endogenous retroviruses (PERVs) represent a special risk because they are integrated in the genome of all pigs and able to infect human cells. In previous preclinical and retrospective clinical trials of xenotransplantation, no transmission of PERV was observed. The first clinical trial of (alginate-encapsulated) porcine islet cell transplantation in New Zealand, which was approved by the New Zealand Government as an open-label phase I/IIa safety/efficacy trial, offers the possibility to analyze microbiological safety in a prospective clinical study. Methods Before the trial started, a multilevel testing strategy was used to screen for 26 microorganisms in donor pigs of the Auckland Island strain and the islet cell preparations used for treatment. Donor testing was performed using molecular methods including multiplex real-time PCR. Blood samples from 14 pig islet cell recipients were also investigated by molecular biological methods at weeks 1, 4, 8, 12, 24, and 52 post-transplant for the transmission of porcine microorganisms. Sera were also monitored at these time points for antibodies against PERVs. Results Beginning in 2009, fourteen patients with severe unaware hypoglycemia were treated with one of four different dosages of alginate-encapsulated porcine islets ranging from 5000–20 000 islet equivalents delivered in a single dose. No transmission of either PERVs or other porcine microorganisms was detected by PCR and immunological methods. Conclusion These findings support previous results and strongly indicate the safety of xenotransplantation as performed here.
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multiplex high resolution melting assay for estimation of porcine endogenous retrovirus perv relative gene dosage in pigs and detection of perv infection in xenograft recipients
Journal of Virological Methods, 2011Co-Authors: Shaun Wynyard, Olga Garkavenko, Robert ElliotAbstract:Porcine Endogenous Retrovirus (PERV) poses an infectious risk in the field of xenotransplantation. This risk may be mitigated by breeding selectively animals bearing favorable PERV genetic characteristics including pigs with low levels of PERV integrated in the genome. A real-time quantitative polymerase chain reaction (PCR) assay employing the Roche High Resolution Melting (HRM) Master was used to estimate the relative gene dosage of PERV pol integrated within the pig genome. When assessed across 99 pigs of the Auckland Island breed numerous animals bearing low gene dosage were identified. The assay was adapted further to perform multiplex PCR for the detection of PERV infection within xenograft recipients. Besides PERV, amplification targets for the multiplex PCR include a pig cell marker for the determination of microchimerism and an internal amplification control (IAC) to assess the efficiency of nucleic acid isolation and effects of PCR inhibition. When 12 patients who had received porcine islet transplants were tested no evidence of PERV infection was found. The assay was shown to be specific, highly reproducible with superior performance over conventional nested PCR. This assay can be used as both a screening tool for PERV proviral levels within donor pigs and as a diagnostic tool to examine PERV transmission in human patients treated with porcine xenotransplantation material.
Joachim Denner - One of the best experts on this subject based on the ideXlab platform.
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No PERV transmission during a clinical trial of pig islet cell transplantation
Virus research, 2016Co-Authors: Vladimir A. Morozov, Shaun Wynyard, Adrian Abalovich, Joachim Denner, Robert B. ElliottAbstract:Xenotransplantation of pig islet cells is a promising alternative for the treatment of diabetes with insulin and may help to prevent numerous late complications such as blindness and amputation. First encouraging results using porcine islets have been reported in preclinical animal models as well in the first clinical trial in New Zealand. The goal of this manuscript is to examine the biological safety of a second trial performed in Argentina, specifically in regards to the transmission of porcine endogenous retroviruses (PERVs) using improved detection methods As in the first trial encapsulated islet cells from the well-characterised Auckland Island pigs were used. The animals were not genetically modified. The islet cells were transplanted in eight human recipients using a modified clinical protocol. Sera taken at different time points after transplantation (up to 55 weeks) were screened for the presence of antibodies against PERV proteins by Western blot analysis using viral antigens from highly purified virus particles. Positive sera obtained by immunization with recombinant PERV proteins were used as control sera. In none of the patients antibodies against PERV were detected, indicating the absence of infection. In parallel at different time points (up to 113 weeks) white blood cells (WBC) have been tested for PERV DNA, and WBC and plasma for PERV RNA by real-time RT-PCR. All tests were negative. In addition, using primers detecting pig mitochondrial cytochrome oxidase (COX) gene, patients were screened for microchimerism. In summary, the data are further evidence for the safety of pig islet cell transplantation.
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microbiological safety of the first clinical pig islet xenotransplantation trial in new zealand
Xenotransplantation, 2014Co-Authors: Shaun Wynyard, Joachim Denner, Olga Garkavenko, Divya Nathu, Robert B. ElliottAbstract:Background Xenotransplantation using pig cells, tissues, or organs may be associated with the transmission of porcine microorganisms and the development of zoonoses. Among all porcine microorganisms porcine endogenous retroviruses (PERVs) represent a special risk because they are integrated in the genome of all pigs and able to infect human cells. In previous preclinical and retrospective clinical trials of xenotransplantation, no transmission of PERV was observed. The first clinical trial of (alginate-encapsulated) porcine islet cell transplantation in New Zealand, which was approved by the New Zealand Government as an open-label phase I/IIa safety/efficacy trial, offers the possibility to analyze microbiological safety in a prospective clinical study. Methods Before the trial started, a multilevel testing strategy was used to screen for 26 microorganisms in donor pigs of the Auckland Island strain and the islet cell preparations used for treatment. Donor testing was performed using molecular methods including multiplex real-time PCR. Blood samples from 14 pig islet cell recipients were also investigated by molecular biological methods at weeks 1, 4, 8, 12, 24, and 52 post-transplant for the transmission of porcine microorganisms. Sera were also monitored at these time points for antibodies against PERVs. Results Beginning in 2009, fourteen patients with severe unaware hypoglycemia were treated with one of four different dosages of alginate-encapsulated porcine islets ranging from 5000–20 000 islet equivalents delivered in a single dose. No transmission of either PERVs or other porcine microorganisms was detected by PCR and immunological methods. Conclusion These findings support previous results and strongly indicate the safety of xenotransplantation as performed here.
