R. W. G. White

Mitochondrial DNA analyses of the red rock lobsterJasus edwardsii supports an apparent absence of population subdivision throughout Australasia

Nucleotide sequence polymorphism in the mitochondrial genomes of 132 adult lobsters (Jasus edwardsil) collected from widespread locales across southern Australia and from New Zealand (April 1989 to June 1990) was assayed, using six restriction endonucleases, to test the hypothesis of a lack of genetic subdivision in a marine species with a long-lived planktonic larva. The mean amount of mtDNA diversity among the 132 mitochondrial genomes was 0.77%. Phenetic clustering and gene-diversity analyses, as well as pairwise comparison of the genetics of specimens from each, or grouped, locales did not detect the presence of genetic subdivision across approx 4600 km of Southern Ocean habitats. The inability of this study to detect population subdivision does not preclude fortutitous, active or habitat-specific larval settlement from producing and maintaining hidden groupings. If genetic homogeneity is maintained in this species by larval dispersal in ocean currents flowing to the east, then westerly populations may deserve special conservation status.

Postsealing genetic variation and population structure of two species of fur seal (Arctocephalus gazella and A. tropicalis)

Commercial sealing in the 18th and 19th centuries had a major impact on the Antarctic and subantarctic fur seal populations (Arctocephalus gazella and A. tropicalis) in the Southern Ocean. The intensive and unrestricted nature of the industry ensured substantial reductions in population sizes and resulted in both species becoming locally extinct at some sites. However, both species are continuing to recover, through the recolonization of islands across their former range and increasing population size. This study investigated the extent and pattern of genetic variation in each species to examine the hypothesis that higher levels of historic sealing in A. gazella have resulted in a greater loss of genetic variability and population structure compared with A. tropicalis. A 316‐bp section of the mitochondrial control region was sequenced and revealed nucleotide diversities of 3.2% and 4.8% for A. gazella and A. tropicalis, respectively. There was no geographical distribution of lineages observed within either species, although the respective ΦST values of 0.074 and 0.19 were significantly greater than zero. These data indicate low levels of population structure in A. gazella and relatively high levels in A. tropicalis. Additional samples screened with restriction endonucleases were incorporated, and the distribution of restriction fragment length polymorphism (RFLP) and sequence haplotypes were examined to identify the main source populations of newly recolonized islands. For A. tropicalis, the data suggest that Macquarie Island and Iles Crozet were probably recolonized by females from Marion Island, and to a lesser extent Ile Amsterdam. Although there was less population structure within A. gazella, there were two geographical regions identified: a western region containing the populations of South Georgia and Bouvetøya, which were the probable sources for populations at Marion, the South Shetland and Heard Islands; and an eastern region containing the panmictic populations of Iles Kerguelen and Macquarie Island. The latter region may be a result of a pronounced founder effect, or represent a remnant population that survived sealing at Iles Kerguelen.

Evidence of stock separation in southern hemisphere organge roughy (Hoplostethus atlanticus, Trachichthyidae) from restriction-enzyme analysis of mitochondrial DNA

Restriction enzyme analysis of mitochondrial DNA (mtDNA) was used to test for genetic homogeneity of orange roughy (Hoplostethus atlanticus) in the southern hemisphere. Two hundred and eighty-six orange roughy specimens were collected from seven general localities: the Great Australian Bight; South Australia (off southeastern Kangaroo Island); the west coast of Tasmania; the east coast of Tasmania; New South Wales; New Zealand and South Africa. Mitochondrial DNA was extracted from developing ovary tissue and analysed with 10 six-base enzymes and 3 four-base enzymes. Both forms of analysis revealed a low level of genetic diversity in this species. The six-base enzyme study found no evidence of reproductively isolated populations of orange roughy in southeastern Australian waters. However, an analysis of 107 fish with 3 four-base enzymes identified at least partial genetic separation of the New South Wales (NSW) sample of orange roughy from South Australian (off southeastern Kangaroo Island) and Tasmanian samples. This finding supports biological evidence for the presence of a distinct subpopulation of orange roughy in NSW waters. The four-base study also provided evidence of the presence of genetically distinct samples of orange roughy occurring in the same localities off southeastern Kangaroo Island from consecutive years. Additional sampling and the use of a greater number of four-base enzymes may be needed to determine if any genetic structuring exists among orange roughy south of New South Wales.

Genetic subdivision of Australian and New Zealand populations of Jasus verreauxi (Decapoda: Palinuridae)—preliminary evidence from the mitochondrial genome

Abstract The palinurid rock lobster, Jasus verreauxi, has a disjunct distribution, occurring on the east coast of Australia and in New Zealand. Oceanic currents flowing across the Tasman Sea from Australia towards New Zealand and the long life of phyllosoma larvae suggests larval mixing and, consequently, genetic similarity between these populations. However, restriction endonuclease analysis of the mitochondrial DNA (mtDNA) of 25 late juvenile and adult lobsters showed that Australian and New Zealand haplotype assemblages are defined by two restriction sites, one confined to each locality. Genetic differentiation between Australian and New Zealand J. verreauxi was also supported by gene diversity analysis (GST). In contrast to the results from a similar study of a congeneric species with an analogous distribution (J. edwardsii), these preliminary results suggest that larval exchange between adult populations across the Tasman Sea may be limited.

Genetic identification of asteroid larvae from Tasmania, Australia, by PCR–RFLP

Studies of seastar larvae in the Derwent River (Tasmania) were hampered by identification uncertainties. A genetic test was developed, based on PCR amplification of a 1300 bp mitochondrial DNA region followed by digestion with three restriction enzymes. The restriction profiles of adults of 14 seastar species were determined. The test was validated for larvae as laboratory‐raised larvae of two species had the appropriate composite haplotypes. Approximately 80% of planktotrophic seastar larvae from Derwent River plankton samples were identified as the recently introduced northern Pacific seastar, Asterias amurensis. The two other larval seastars identified were Coscinasterias muricata and Patiriella regularis.

Cytotaxonomy of seven species of Galaxias (Pisces: Galaxiidae) in Tasmania

Karyotypes of 7 species of the genus Galaxias in Tasmania are compared and a phylogenetic interpretation of these data offered. Species fall into 3 distinct groups, viz. those with 2n=44 (G. brevipinnis, G. johnstoni and G. fontanus), those with 2n=32 (G. truttaceus, G. tanycephalus and G. auratus), and G. maculatus with 2n=22. Land-locking appears to have been a major evolutionary force. G. johnstoni and G. fontanus are most likely land-locked derivatives of the ancestral G. brevipinnis. G. tanycephalus and G. auratus are almost certainly land-locked derivatives of the ancestral G. truttaceus. G. maculatus has a specialized karyotype which may have been derived from a G. truttaceus-like complement by 5 Robertsonian centric fusions. It is postulated that the original stock ancestral to the 7 species examined was G. brevipinnis-like. Species relationships suggested from previous classical morphological investigations are supported by the present study.

Threatened fishes of the world: Galaxias auratus Johnston, 1883 (Galaxiidae)

Common name: Golden galaxias. Conservation status: Rare – (Tasmanian Threatened Species Protection Act 1995); Endangered – ASFB (2003). Identification: D 7–10, A 11–12, P 14–18, vertebral count 53–56 (McDowall & Frankenberg 1981). Small scaleless salmoniform fish, maximum size: 240 mm TFL, 130 g (Hardie 2003). Colouration: golden to olive-green on dorsal surface and sides, silvery-grey on ventral surface. Back and sides are covered with round to oval black spots (McDowall & Frankenberg 1981). Drawing by Carol Kroger in Fulton (1990).

The effects of turbidity and complex habitats on the feeding of a galaxiid fish are clear and simple

The habitat used by animals plays an important role in their interactions with predators and prey. By using complex habitats such as areas of dense macrophyte cover in response to elevated predation risk, small fishes may reduce their foraging success. Because the threat of predation by introduced brown trout increases the use of complex habitats by the threatened Galaxias auratus (Johnston), we experimentally examined its foraging in different habitats to estimate indirect impacts of brown trout presence. The lakes in which G. auratus lives have recently become more turbid, so the experiment was also conducted under different turbidity levels. Laboratory feeding trials in which planktonic and epibenthic prey were simultaneously offered to G. auratus in the presence or absence of artificial macrophytes and at three turbidity levels (0, 50 and 100 NTU) revealed that its overall foraging success was unaffected by habitat complexity; however, in trials with artificial macrophytes, G. auratus consumed a greater proportion of planktonic prey than in the absence of artificial macrophytes. Neither overall foraging success nor prey selection by G. auratus was affected by high turbidity, indicating that water clarity does not appear to directly negatively impact its feeding. The switch in prey types would probably not be detrimental to G. auratus in the long term, and thus it appears that there is no substantial feeding cost associated with its increased use of complex habitats. It could, however, affect lower trophic levels in the lakes to which it is endemic.

Trichodinid parasites (Ciliophora: Peritricha) from the gills of some Australian marine fishes

Three species of the genus Trichodina are reported from the gills of marine fishes in south-eastern Tasmania, Australia. Two of these species are new: T. australis n. sp. from five atherinid fish species, Atherinosoma microstoma, Leptatherina presbyteroides, Kestratherina brevirostris, K. esox and K. hepsetoides; and T. nesogobii n. sp. from Nesogobius sp. 1. One previously reported species, T. jadranica Raabe, 1958, was also found on Nesogobius sp. 1.

Genetic variation in the greenback flounder Rhombosolea tapirina Günther (Teleostei, Pleuronectidae) and the implications for aquaculture

Samples of the greenback flounder, Rhombosolea tapirina, were collected from five Tasmanian sites and from one site each off Victoria and New Zealand. Thirty enzyme-coding loci were analysed by gel electrophoresis. Seventeen loci were variable, nine of which were polymorphic in at least four samples. Average heterozygosity across all 30 loci was relatively high at 0.086 ± 0.032. There were significant genetic differences between the Australian and New Zealand samples, with a genetic distance of 0.041, which was an order of magnitude larger than that observed between any Australian samples. Samples from the west coast of Tasmania and from Victoria were genetically isolated from each other and from the remaining four Tasmanian samples; the latter showed little variation among themselves. Reductions in genetic variation (heterozygosity and alleles) were observed in two cultured cohorts when compared with the wild-caught samples, with corresponding low estimates of effective population sizes compared with putative breeding numbers. No genetic variation was detected between normal and malpigmented individuals from the same culture cohort.