scholarly journals Risk Factors for New Zealand Sea Lion (Phocarctos hookeri) Pup Mortality: Ivermectin Improves Survival for Conservation Management

2021 ◽  
Vol 8 ◽  
Author(s):  
Sarah A. Michael ◽  
David T. S. Hayman ◽  
Rachael Gray ◽  
Wendi D. Roe

Septicaemia due to hypervirulent (HV) Klebsiella pneumoniae is the leading cause of neonatal pup mortality in endangered New Zealand sea lions (Phocarctos hookeri) at Enderby Island, in the New Zealand sub-Antarctic. Accounting for approximately 60% of annual pup mortality at this site following an epizootic event in 2001–02, HV K. pneumoniae is also emerging worldwide as a significant community-acquired human pathogen. To facilitate efficient direct mitigation to reduce pup mortality, a case-control study and prospective cohort study were conducted to identify risk factors amenable to active management. Additionally, to investigate impacts of hookworm (Uncinaria spp.), a nested treatment trial with the anthelmintic ivermectin was undertaken concurrently. During two austral summer field seasons (2016–2018), 698 pups were captured for treatment trial recruitment and the collection of morphometric measurements, biological samples and risk factor data. Gastrointestinal carriage of the virulent phenotype of K. pneumoniae was a consistent risk factor, while ivermectin treatment and higher body condition index consistently reduced risk of HV K. pneumoniae mortality. Significantly fewer ivermectin-treated pups were found dead (24.1% control, 11.1% treatment), with a trend towards a higher proportion of HV K. pneumoniae deaths amongst the control group. This study provides evidence to support ivermectin treatment as a pup mortality mitigation strategy in New Zealand sea lions at Enderby Island. If applied to larger colonies where HV K. pneumoniae and hookworm impact pup survival, this intervention could have population-scale benefits for this endangered species. Further work is required to understand how ivermectin prevents HV K. pneumoniae septicaemia, but removal of hookworms before intestinal mucosal damage occurs could limit systemic spread of virulent bacteria from the gastrointestinal tract.

PLoS ONE ◽  
2019 ◽  
Vol 14 (11) ◽  
pp. e0225461
Author(s):  
Sarah A. Michael ◽  
David T. S. Hayman ◽  
Rachael Gray ◽  
Ji Zhang ◽  
Lynn Rogers ◽  
...  

2007 ◽  
Vol 43 (3) ◽  
pp. 461-474 ◽  
Author(s):  
A. Castinel ◽  
P. J. Duignan ◽  
W. E. Pomroy ◽  
N. López-Villalobos ◽  
N. J. Gibbs ◽  
...  

2016 ◽  
Vol 53 (6) ◽  
pp. 1241-1247 ◽  
Author(s):  
S. A. Michael ◽  
B. L. Chilvers ◽  
S. A. Hunter ◽  
P. Duignan ◽  
W. Roe

2000 ◽  
Vol 203 (23) ◽  
pp. 3655-3665 ◽  
Author(s):  
D.P. Costa ◽  
N.J. Gales

The New Zealand sea lion, Phocarctos hookeri, is the deepest- and longest-diving sea lion. We were interested in whether the diving ability of this animal was related to changes in its at-sea and diving metabolic rates. We measured the metabolic rate, water turnover and diving behavior of 12 lactating New Zealand sea lions at Sandy Bay, Enderby Island, Auckland Islands Group, New Zealand (50 degrees 30′S, 166 degrees 17′E), during January and February 1997 when their pups were between 1 and 2 months old. Metabolic rate (rate of CO(2) production) and water turnover were measured using the (18)O doubly-labeled water technique, and diving behavior was measured with time/depth recorders (TDRs). Mean total body water was 66.0+/−1.1 % (mean +/− s.d.) and mean rate of CO(2) production was 0. 835+/−0.114 ml g(−)(1)h(−)(1), which provides an estimated mass-specific field metabolic rate (FMR) of 5.47+/−0.75 W kg(−)(1). After correction for time on shore, the at-sea FMR was estimated to be 6.65+/−1.09 W kg(−)(1), a value 5.8 times the predicted standard metabolic rate of a terrestrial animal of equal size. The mean maximum dive depth was 353+/−164 m, with a mean diving depth of 124+/−36 m. The mean maximum dive duration was 8.3+/−1.7 min, with an average duration of 3.4+/−0.6 min. The deepest, 550 m, and longest, 11.5 min, dives were made by the largest animal (155 kg). Our results indicate that the deep and long-duration diving ability of New Zealand sea lions is not due to a decreased diving metabolic rate. Individual sea lions that performed deeper dives had lower FMRs, which may result from the use of energetically efficient burst-and-glide locomotion. There are differences in the foraging patterns of deep and shallow divers that may reflect differences in surface swimming, time spent on the surface and/or diet. Our data indicate that, although New Zealand sea lions have increased their O(2) storage capacity, they do not, or cannot, significantly reduce their at-sea metabolic rates and are therefore likely to be operating near their physiological maximum.


2008 ◽  
Vol 35 (5) ◽  
pp. 463 ◽  
Author(s):  
B. Louise Chilvers ◽  
Ian S. Wilkinson

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.


2012 ◽  
Vol 93 (4) ◽  
pp. 1006-1016 ◽  
Author(s):  
Federico G. Riet-Sapriza ◽  
PÁdraig J. Duignan ◽  
B. Louise Chilvers ◽  
Ian S. Wilkinson ◽  
Nicolás Lopez-Villalobos ◽  
...  

2015 ◽  
Vol 97 (2) ◽  
pp. 436-443 ◽  
Author(s):  
Catherine J. Collins ◽  
B. Louise Chilvers ◽  
Matthew Taylor ◽  
Bruce C. Robertson

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.


2005 ◽  
Vol 83 (5) ◽  
pp. 642-648 ◽  
Author(s):  
B Louise Chilvers ◽  
Bruce C Robertson ◽  
Ian S Wilkinson ◽  
Padraig J Duignan ◽  
Neil J Gemmell

Sexual aggression by male pinnipeds during breeding can lead to female injury and death, affecting reproductive success, fecundity, and increasing the cost of mating for females. Thus, females that employ strategies to minimize the probability of being injured will be at an advantage. Here we investigate the extent of injuries and the number of deaths attributed to male harassment, and test the hypothesis of whether the arrival and departure behaviour of female New Zealand sea lions (Phocarctos hookeri (Gray, 1844); NZSL) at Sandy Bay, Enderby Island, the Auckland Islands, is adapted to reduce the chance of injury or death from encounters with male NZSLs. During the breeding season, harassment by non-territorial male NZSLs causes mortality in adult female NZSLs, approximately 5 in every 1000 females breeding each year. Permanent scars from male bites are observed on 84% of adult females. This mortality and visible injury rate only represents the direct impacts on female NZSL from male harassment. Indirect impacts, such as the time and energy cost of avoidance behaviour, pup separation, and pup injury and death, can have as significant long-term effects on individuals and the population. We find that male harassment can influence the behaviour of individuals in NZSL breeding harems.


Polar Biology ◽  
2020 ◽  
Vol 43 (12) ◽  
pp. 2031-2042
Author(s):  
B. Louise Chilvers ◽  
Jacinda M. Amey ◽  
Daniel P. Costa

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