Academic literature on the topic 'Port Jackson shark – Reproduction'

Restricted gene flow and reproductive philopatry are increasingly being described in marine predators such as sharks. However, observing shark reproductive behaviour in situ is problematic because of issues associated with sampling in the marine environment. As such, molecular tools have become fundamental to unravelling complex mating behaviours. In this study, we examined patterns of genetic structure in the oviparous Port Jackson shark (Heterodontus portusjacksoni) using 10 microsatellite loci and the mitochondrial (mt)DNA control region. Patterns of genetic structure were investigated between breeding aggregations in Sydney and Jervis Bay, as well as between two sites within Jervis Bay. Significant genetic differentiation was detected between Sydney and Jervis Bay using mtDNA, but no structure was observed within Jervis Bay. No significant genetic differentiation was found with microsatellites within or between aggregations. Mean assignment index values were significantly higher for females than males in Jervis Bay, but not in Sydney. Both females and males migrate inshore during the Austral winter for breeding, but it appears females may exhibit higher levels of reproductive philopatry than males. This is the first study to document reproductive philopatry in an oviparous shark, highlighting the importance of conserving and appropriately managing breeding sites for H. portusjacksoni and potentially other oviparous shark species.

one of 353 port jackson sharks, heterodontus portusjacksoni, caught off the southern coast of western australia, was a hermaphrodite. the female reproductive tract consisted of a large (functional) right ovary with three large yolked ova, a small non-functional left ovary and two well-developed uteri and oviducal glands. the male tract comprised two conspicuous but undeveloped testes, two vas deferens and two calcified claspers with grooves. this individual represents the first published example of hermaphroditism in the order heterodontiformes and is a rare example of an elasmobranch with a complete suite of both male and female reproductive structures.

Demographic analyses are used to assess the status and vulnerability of elasmobranchs but their accuracy is often affected by limited basic biological information. Although the Port Jackson shark Heterodontus portusjacksoni (Meyer) is currently not considered at threat, there is insufficient data for eastern Australia to assess this rigorously. The present study determined vital demographic rates of adult and juvenile H. portusjacksoni at four locations on the central and southern coast of New South Wales, Australia from January 2002 to December 2005 using underwater visual census, tag–recapture and samples obtained from a commercial fishery. Natural mortality was low in adults (0.063–0.074 year–1) and juveniles (0.225 year–1), but substantial at the embryonic stage (0.783–0.896 year–1). Adult growth rates (31.4–32.7 mm year–1) were slightly less than that of juveniles (36.8–37.5 mm year–1). Males at both stages grew slightly faster than females. However, H. portusjacksoni had slower growth rates than many other elasmobranch species. Having a low intrinsic rate of increase (r = 0.069 year–1), long generation times (μ1 = 22.5 year) and a low rebound potential, adults are the stage with the greatest impact on population growth. Hence, their life history strategy makes them susceptible to serious decline under exploitation, and management should strive to maintain the adult reproductive stock as a priority.

Knowledge of the broad-scale movement patterns of sharks is essential to developing effective management strategies. Currently there is a large bias in studies focusing on species that are either large apex predators or found in tropical to subtropical regions. There is limited knowledge of the movements and migrations of benthic and temperate shark species. The present study used passive acoustic telemetry to investigate the movement patterns of a benthic shark species, the Port Jackson shark (Heterodontus portusjacksoni). Individuals were tagged with acoustic transmitters between 2012 and 2014 and their movements were monitored within Jervis Bay and along the east Australian coastline for up to 4 years. Male and female Port Jackson sharks demonstrated high levels of philopatry to both Jervis Bay and their tagging location across multiple years. Although males and females did not differ in their arrival times, females departed from Jervis Bay later than males. Approximately half the tagged individuals migrated in a southward direction, with individuals being detected at Narooma, Bass Strait and Cape Barron Island. This study provides conclusive evidence of bisexual philopatry in a benthic temperate shark species, confirming previous hypotheses, and presents the most detailed migration route for Port Jackson sharks to date.

Commercial fisheries can discard a considerable volume of sharks and rays, which, as a group, are of high conservation concern. In Western Australia (WA), commercial shark fishing commenced in the 1940s; however, catch time series are not available for discarded species. The present study quantified catch (i.e. dead individuals) time series of discarded sharks and rays in WA’s shark fisheries using on-board observer information collected since 1993 and testing assumptions through sensitivity analysis. Overall, 18 shark and ray taxonomic groups were discarded, comprising ~20% of the observed catch by number. Port Jackson shark, southern eagle ray and spurdogs were the most commonly discarded elasmobranchs, followed by western wobbegong, angel sharks, stingrays, and guitarfish and shovelnose rays. For the base case scenario, the catch of these species was small, peaking at 12.6, 5.6, 1.3, 1.8, 4, 1.3 and 2.7 tonnes (Mg) respectively, given their low post-release mortality (PRM). Current catch levels were even lower (e.g. <5 Mg for Port Jackson shark). Other discarded elasmobranchs were rarely caught. Assuming 100% PRM resulted in higher annual catches, highlighting the need for further research on the PRM of sharks and rays. The reconstructed catch series will be used in risk assessments to determine the sustainability of discarded species.

Port Jackson sharks are distributed throughout southern Australia, with evidence suggesting that potential subpopulations exist. If subpopulations are evident, then phenotypic variation among groups should result in differences in life-history parameters. The present study tested for patterns of spatial variability of life-history parameters among regional Port Jackson shark populations. Rates of growth from Port Jackson sharks caught in the gulf waters of South Australia were calculated on the basis of counts of vertebral increments. Growth parameters were obtained by fitting the length-at-age data to von Bertalanffy and Gompertz growth functions. While the derived growth curves fit the length-at-age data well (r2 ranged from 0.87 to 0.91), parameters showed considerable differences between the two functions, with the von Bertalanffy function providing the more realistic estimates of growth (combined sexes: k = 0.081 year–1, L∞ = 1232 mm total length and t0 = –1.937 years). Life-history parameters for South Australian Port Jackson sharks were collated with the available data for the species, facilitating comparisons among regional populations. Growth curves among populations varied significantly; however, considerable overlap in the length ranges of size at birth and sizes at maturity among populations were evident. Overall, the data presented here do not provide definitive support for the presence of subpopulations across the distribution of the Port Jackson shark, suggesting that molecular analysis maybe required to directly test for structuring.

SCUBA observations show that Port Jackson sharks repeatedly visit specific resting sites on ocean reefs at South Bondi (New South Wales) and, when disturbed, move directly from one site to another. The sharks also use specific resting sites in Sydney Harbour and, when transferred by boat to different localities within the harbour, up to 3 km away, return to their original resting sites. The sharks migrate from as far south as Tasmania to Sydney Harbour to lay their eggs in specific sites. Speculative extrapolation from the above observations suggests that Port Jackson sharks must have a highly developed spatial memory.

Research Doctorate - Doctor of Philosophy (PhD)
World shark populations are declining rapidly from the increased demand for shark meat and fins and from their capture as by-catch. Techniques to accurately and reliably estimate the age of elasmobranchs are required to understand life history and develop management strategies. Although some biological information exists for the harvested species, few of the many shark species caught as by-catch have been investigated. In the waters of New South Wales, Australia, the Port Jackson shark (Heterodontus portusjacksoni) is a non-targeted species, however it is a major contributor to the elasmobranch by-catch in the bottom trawl and prawn fisheries. Although some biological and ecological information exists on Port Jackson sharks from New South Wales, there is no understanding of suitable techniques to age this species and of the age structure of the New South Wales’ population. Hence, the main purpose for the present study was to determine a suitable technique to age Port Jackson sharks and thereby provide essential age and growth data for its future management, sustainable use and conservation. This study consisted of research into: (1) the macroscopic anatomy of the vertebral centra and dorsal spines from 652 H. portusjacksoni to explore their suitability as ageing structures; (2) a comparison of whole and sectioned vertebral centra and of whole and sectioned dorsal spines for ageing; (3) validation of the annual formation of growth bands; (4) a comparison of the effect of prior experience on readers’ ability to count annual growth bands in vertebral centra; and (5) the development of age-growth models for the New South Wales’ population of H. portusjacksoni. Two types of vertebral centra (trunk and caudal vertebrae) were found in the vertebral column. Both vertebrae consisted of a centrum, 2 ribs, 4 neural arches, basiopophyses and neural foramen and decreased in size from anterior to posterior. A strong linear relationship was identified between vertebral diameter (VD) and fork length (FL). Each dorsal spine was positioned anterior to the dorsal fin and consisted of a stem and the cap. A strong linear relationships were identified between spine base width (SBW) and FL. The existence of alternating opaque and translucent band pairs in both structures further suggested they may be suitable for ageing purposes. Validation (calcein and oxytetracycline injections, marginal increment analysis, and centrum edge analysis) confirmed that translucent band pairs were formed during the winter (September-November) and were annual in both vertebral centra and dorsal spines. Whole and sectioned vertebral centra and dorsal spines were individually examined to determine which method best estimated the age. Although both methods had individual low reading bias and high precision, there was a difference between the two methods. The average bias between the two methods using vertebral centra was -0.158 ±0.05 and the coefficient of variance (CV) was 92.32% for females and -0.157 ±0.03 and CV was 56.95% for males. This indicated that sectioned vertebral centra returned higher ages than whole vertebral centra. When comparing whole dorsal spine age estimates to sectioned dorsal spines, there was an average bias between methods of -0.22 ±0.026 and a low precision 73.09%. Again indicating that sectioned dorsal spines returned higher ages than whole dorsal spines. A comparison of ages estimated from sectioned vertebral centra and sectioned dorsal spines showed that vertebral centra aged older than dorsal spines. Although the two structures each had low reading bias and high reading precision, there were differences between the two structures. The average bias between the two structures was -0.4 ±0.03 and the CV was low (74.7%), indicating that there was a significant difference in age derived from the two structures. Therefore, great caution should be taken when choosing which structure to use for age estimation. Ages of sharks estimated from the recommended sectioned vertebral centra ranged from 0.2 to 32.5 years for females and 0.2 to 23.8 years for males. Four different growth models were compared using both sectioned vertebral centra and sectioned dorsal spines to estimate the best suitable growth curve. Out of the 4 growth models the Gompertz Growth Function (GGF) best described the growth of H. portusjacksoni. von Bertalanffy growth parameters estimated from ageing data using the GGF for females were t0 = 2.584 yr, k = 0.111, L∞ = 1134.1 mm FL, and for males t0 = 1.629 yr, k = 0.131, L∞ = 1012.9 mm FL. This indicates that H. portusjacksoni has a slow growth rate and a longer life span than most other elasmobranch species. The effect of reader’s experience on the bias and precision of age estimates of sectioned vertebral centra was determined in an experiment that compared the author (an experienced vertebral centra reader) with an experienced fish otolith reader, two readers recently trained in reading vertebral centra (but lacking experience), and two untrained and inexperienced readers. Bias and precision were determined for each reader from two ageing trials with the same structure three months apart. Between-trials bias for each reader (except the author)ranged from 0.033 to 0.13 and precision ranged from 8.2 to 19.5%, while the author had low bias 0.006 and high precision 1.1%. When comparing all the readers with the author, bias ranged from 0.033 to 0.13 with an 8.2 to 19.5% precision for trial one, and 0.017 to 0.5 with precision between 2.5 to 5.4% in trial two. The age-bias plots comparing the two trials all indicated that only the author was consistent. And the age-bias plots between the author and the other readers all indicated that neither experience in ageing teleost otoliths or limited training in ageing enhanced the bias or precision compared to inexperienced elasmobranch agers.

Research Doctorate - Doctor of Philosophy (PhD)
World shark populations are declining rapidly from the increased demand for shark meat and fins and from their capture as by-catch. Techniques to accurately and reliably estimate the age of elasmobranchs are required to understand life history and develop management strategies. Although some biological information exists for the harvested species, few of the many shark species caught as by-catch have been investigated. In the waters of New South Wales, Australia, the Port Jackson shark (Heterodontus portusjacksoni) is a non-targeted species, however it is a major contributor to the elasmobranch by-catch in the bottom trawl and prawn fisheries. Although some biological and ecological information exists on Port Jackson sharks from New South Wales, there is no understanding of suitable techniques to age this species and of the age structure of the New South Wales’ population. Hence, the main purpose for the present study was to determine a suitable technique to age Port Jackson sharks and thereby provide essential age and growth data for its future management, sustainable use and conservation. This study consisted of research into: (1) the macroscopic anatomy of the vertebral centra and dorsal spines from 652 H. portusjacksoni to explore their suitability as ageing structures; (2) a comparison of whole and sectioned vertebral centra and of whole and sectioned dorsal spines for ageing; (3) validation of the annual formation of growth bands; (4) a comparison of the effect of prior experience on readers’ ability to count annual growth bands in vertebral centra; and (5) the development of age-growth models for the New South Wales’ population of H. portusjacksoni. Two types of vertebral centra (trunk and caudal vertebrae) were found in the vertebral column. Both vertebrae consisted of a centrum, 2 ribs, 4 neural arches, basiopophyses and neural foramen and decreased in size from anterior to posterior. A strong linear relationship was identified between vertebral diameter (VD) and fork length (FL). Each dorsal spine was positioned anterior to the dorsal fin and consisted of a stem and the cap. A strong linear relationships were identified between spine base width (SBW) and FL. The existence of alternating opaque and translucent band pairs in both structures further suggested they may be suitable for ageing purposes. Validation (calcein and oxytetracycline injections, marginal increment analysis, and centrum edge analysis) confirmed that translucent band pairs were formed during the winter (September-November) and were annual in both vertebral centra and dorsal spines. Whole and sectioned vertebral centra and dorsal spines were individually examined to determine which method best estimated the age. Although both methods had individual low reading bias and high precision, there was a difference between the two methods. The average bias between the two methods using vertebral centra was -0.158 ±0.05 and the coefficient of variance (CV) was 92.32% for females and -0.157 ±0.03 and CV was 56.95% for males. This indicated that sectioned vertebral centra returned higher ages than whole vertebral centra. When comparing whole dorsal spine age estimates to sectioned dorsal spines, there was an average bias between methods of -0.22 ±0.026 and a low precision 73.09%. Again indicating that sectioned dorsal spines returned higher ages than whole dorsal spines. A comparison of ages estimated from sectioned vertebral centra and sectioned dorsal spines showed that vertebral centra aged older than dorsal spines. Although the two structures each had low reading bias and high reading precision, there were differences between the two structures. The average bias between the two structures was -0.4 ±0.03 and the CV was low (74.7%), indicating that there was a significant difference in age derived from the two structures. Therefore, great caution should be taken when choosing which structure to use for age estimation. Ages of sharks estimated from the recommended sectioned vertebral centra ranged from 0.2 to 32.5 years for females and 0.2 to 23.8 years for males. Four different growth models were compared using both sectioned vertebral centra and sectioned dorsal spines to estimate the best suitable growth curve. Out of the 4 growth models the Gompertz Growth Function (GGF) best described the growth of H. portusjacksoni. von Bertalanffy growth parameters estimated from ageing data using the GGF for females were t0 = 2.584 yr, k = 0.111, L∞ = 1134.1 mm FL, and for males t0 = 1.629 yr, k = 0.131, L∞ = 1012.9 mm FL. This indicates that H. portusjacksoni has a slow growth rate and a longer life span than most other elasmobranch species. The effect of reader’s experience on the bias and precision of age estimates of sectioned vertebral centra was determined in an experiment that compared the author (an experienced vertebral centra reader) with an experienced fish otolith reader, two readers recently trained in reading vertebral centra (but lacking experience), and two untrained and inexperienced readers. Bias and precision were determined for each reader from two ageing trials with the same structure three months apart. Between-trials bias for each reader (except the author)ranged from 0.033 to 0.13 and precision ranged from 8.2 to 19.5%, while the author had low bias 0.006 and high precision 1.1%. When comparing all the readers with the author, bias ranged from 0.033 to 0.13 with an 8.2 to 19.5% precision for trial one, and 0.017 to 0.5 with precision between 2.5 to 5.4% in trial two. The age-bias plots comparing the two trials all indicated that only the author was consistent. And the age-bias plots between the author and the other readers all indicated that neither experience in ageing teleost otoliths or limited training in ageing enhanced the bias or precision compared to inexperienced elasmobranch agers.