Metazoan parasites threaten the development and expansion of yellowtail kingfish (Seriola lalandi) sea-cage aquaculture in Australia. There is international speculation that parasite transmission from farmed to wild fish leads to increased incidence of parasitism in wild fish. Conversely, transfer of parasites from wild fish to farmed fish can negatively impact upon the health of farmed fish. Baseline information on the parasite assemblage of wild S. lalandi in Australia will: 1) allow informed judgments to be made in order to responsibly monitor, and perhaps remedy, potentially negative impacts and; 2) enable identification of parasite species of potential harm to the Australian S. lalandi aquaculture industry. I collected wild Seriola spp. (Carangidae) throughout southern Australia and examined them for metazoan parasites. Fifty-six metazoan parasite species are identified, including one new species. A taxonomic listing is provided for the metazoan parasites found. Taxonomic descriptions are made for the blood fluke Paradeontacylix godfreyi n. sp. (Digenea: Sanguinicolidae) and a redescription is provided for the parasitic copepod Naricolax chrysophryenus (Cyclopoida: Bomolochidae). A qualitative risk assessment was devised for the metazoan parasite taxa identified for the sea-cage aquaculture of S. lalandi in South Australia. Risk was interpreted considering the likelihood and consequence of parasite establishment and proliferation. The monogeneans Benedenia seriolae and Zeuxapta seriolae were considered extremely likely to establish and proliferate. Benedenia seriolae also poses high potential negative consequences for cost-effective S. lalandi sea-cage farming. However, the absence of potential mitigation methods and parasite management for Paradeontacylix spp. (Digenea), Kudoa sp. and Unicapsula seriolae (Myxozoa) indicates that these species may also present high negative consequences for S. lalandi aquaculture in Australia. The nature of wild Seriola migrations is critical for an understanding of the potential impact of disease and parasite interactions between wild and farmed fish. A small-scale tagging programme of wild-caught S. lalandi and S. hippos in South Australia provided insight into the movements of these species. Recapture results indicate that large S. lalandi remain in, or return to, northern Spencer Gulf. S. lalandi also move past sea-cage farms in Fitzgerald Bay, northern Spencer Gulf, which is an important consideration in view of potential expansion of the S. lalandi sea-cage industry in Spencer Gulf. There is surprisingly little experimental assessment on parasite transmission from farmed fish to wild fish. Studies assessing parasite interactions between wild and cultured fish employ models to quantify parasite population levels of cultured, wild and escaped fish, while others carry out comparative surveys of parasite prevalence and intensity over time, in areas close to and distant from farming activity. I provide preliminary data on ectoparasite prevalence and intensity on wild S. lalandi in areas close to, distant from and where there is no sea-cage farming in southern Australia. I review methods employed in the northern hemisphere to assess sea-louse transfer between wild and farmed salmon and propose methods for assessing monogenean parasite transmission from farmed to wild S. lalandi in Australia. In summary, this thesis provides insight into the potential for parasite interactions between wild and farmed S. lalandi. I document the parasite assemblage of wild and farmed S. lalandi and wild S. hippos and provide baseline data on ‘natural’ parasite prevalence and intensity. I provide a taxonomic description of a new species of blood fluke. I indicate the likelihood of parasite transfer from wild fish to farmed S. lalandi, and identify parasite taxa with potentially negative consequences for sea-cage aquaculture. I provide the first firm data that wild S. lalandi move past one area where kingfish are farmed in sea-cages in South Australia. Finally, I propose procedures to better understand the potential for monogenean parasite transmission from farmed S. lalandi to wild fish. This thesis reports new information that is important when considering and managing expansion of the S. lalandi sea-cage aquaculture industry throughout Australia. It also provides baseline data on natural parasite levels to enable ongoing monitoring of the potential impacts of the industry on wild fish populations. / http://proxy.library.adelaide.edu.au/login?url= http://library.adelaide.edu.au/cgi-bin/Pwebrecon.cgi?BBID=1294807 / Thesis (Ph.D.) -- University of Adelaide, School of Earth and Environmental Sciences, 2007

This thesis is inspired by the historical principles of RG Collingwood, an historiographer whose precepts are recurrently cited herein. It is the life and times style biography of Francesco Giovanni Fantin, born San Vito de Leguzzano in the Schio district of the Province of Vicenza in the Veneto region of Italy 20 January 1901, died Loveday Internment Camp Compound 14A, South Australia 16 November 1942. SA police at the time found that Fantin was assassinated by fascist conspirators who contrived to intimidate witnesses and interfere with material evidence, (findings here confirmed) frustrating the laying of a charge of murder and leading in March 1943 to the sentencing of Giovanni Casotti to two years hard labour for manslaughter in the Supreme Court of South Australia. (Casotti was subsequently deported.) This thesis begins with the reconstruction of Fantin’s origins in one of the rural crucibles of Italian capitalism and industrialism. The presence of anarchist traditions in the Province and in Fantin’s immediate circle in the late nineteenth and early twentieth centuries is documented. The history of the Great War, the Red Biennium and the Rise of Fascism in the Schio district is then reconstructed in connection with Fantin’s formative years, with particular reference to the role of the textile strike of 1921 as the precursor to the political and mass emigration from the district to Australia of which Fantin was a humble protagonist. Fantin’s years as an antifascist activist in exile in Australia are then rehearsed as an essential prerequisite for understanding why he was selected for assassination. The thesis closes with a detailed reconstruction of how his death was encompassed and its political implications managed by Dr HV Evatt. An Iconographic Appendix and Bibliography follow. / http://proxy.library.adelaide.edu.au/login?url= http://library.adelaide.edu.au/cgi-bin/Pwebrecon.cgi?BBID=1331596 / Thesis (Ph.D.) -- University of Adelaide, School of Economics, 2008

Title page, contents and abstract only. The complete thesis in print form is available from the University of Adelaide Library. / The aims of this investigation on the Holocene carbonate successions of three shallow, ephemeral lakes from the Cooring coastal plain were: to determine the timing of the sapropel ’events’ in the three lakes; to determine the origin of the sapropelic organic matter and evaluate changes; to establish whether sapropel deposition in these shallow, coastal lakes primarily reflects increased organic matter delivery to the sediments during periods of enhanced terrestrial input and/or aquatic productivity, and; to relate sapropel deposition in these three lakes to both regional and global palaeoenvironment reconstructions. --p. 23-24. / http://proxy.library.adelaide.edu.au/login?url= http://library.adelaide.edu.au/cgi-bin/Pwebrecon.cgi?BBID=1324064 / Thesis (Ph.D.) -- University of Adelaide, School of Earth and Environmental Sciences, 2007

This study investigates early life stages of the southern sea garfish (Hyporhamphus melanochir) and their association with seagrass in Gulf St Vincent, South Australia. The overall aims were to identify and describe the early life stages of H. melanochir and to explore the possible relationship(s) between these life stages and seagrass habitat with the emphasis on seagrass as a requirement for spawning or as a food source. The reproductive biology of female H. melanochir from the commercial fishery was assessed by microscopic examination of ovaries, oocyte size distributions, gonadosomatic indices, and macroscopic ovarian stages. Five stages of oocyte development were identified and described: perinucleolar, yolk vesicle, yolk globule, migratory nucleus and hydrated. A coherence between histological and whole oocyte descriptions is demonstrated. Hyporhamphus melanochir are characterised as multiple spawners with group-synchronous oocyte development and indeterminate fecundity. A protracted spawning season from October to March was indicated by the occurrence of ripe ovaries and increases in gonadosomatic index. Females reach sexual maturity at 193 mm standard length, and batch fecundity ranged from 201-3044 oocytes depending on fish size. Spawning shoals are segregated by sex, as indicated by commercial samples, with a biased female-to-male ratio of 4.5:1 during the spawning season (1.2:1 during the non-spawning season). In addition, features of the oocyte surface were closely examined, which revealed that the filaments on the chorion of the hydrated oocyte are adhesive. These adhesive filaments presumably allow the fertilised egg to become attached to vegetative substrate by adhesion and/or entanglement. H. melanochir larvae were discriminated from another hemiramphid species, river garfish (H. regularis), which is also known to occur in the study area, based on species-specific amplification of part of the mitochondrial control region using a multiplex polymerase chain reaction (PCR) assay. The species were easily discerned by the number and distinct sizes of PCR products [H. melanochir, 443 bp; river garfish (H. regularis), 462 and 264 bp]. Although based on a single gene, this molecular method will correctly identify the species of individuals in at least 96% and 94% of tests for H. melanochir and H. regularis, respectively. Subsequent to verifying the identification of species by molecular discrimination, the larval development of H. melanochir and H. regularis were described. Larvae of H. melanochir and H. regularis had completed notochord flexion at hatching and are characterized by their elongate body with distinct rows of melanophores along the dorsal, lateral and ventral surfaces; small to moderate head; heavily pigmented, long straight gut; persistent preanal finfold; and extended lower jaw. Fin formation occurs in the sequence: caudal, dorsal and anal (almost simultaneously), pectoral, pelvic. Despite the similarities between both species and among hemiramphid larvae in general, H. melanochir larvae are distinguishable from H. regularis by: having 58-61 vertebrae (v. 51-54 for H. regularis); having 12-15 melanophore pairs in longitudinal rows along the dorsal margin between the head and origin of the dorsal fin (v. 19-22 for H. regularis); and the absence of a large ventral pigment blotch anteriorly on the gut and isthmus (present in H. regularis). A logistic regression analysis of body measurements also revealed interspecies differences in the combined measurements of eye diameter and pre-anal fin length. Both species can be distinguished from morphologically similar larvae found in southern Australia (other hemiramphids and a scomberosocid) by differences in meristic counts and pigmentation. Hyporhamphus melanochir larvae were successfully collected throughout Gulf St Vincent using a neuston net; however, attempts to sample eggs were unsuccessful. Abundances of larvae in the gulf averaged 4.8 and 12.3 larvae 1000⁻ ² of surface water in December 1998 and December 2000, respectively. Larvae exhibit fast growth, as indicated by otolith growth increments, with backcalculated spawning dates falling within the October-March spawning season. Spatial analysis of larval distributions revealed a positive spatial autocorrelation, i.e. non-randomness or clustering of similar abundance values. Most larvae were found in the upper region of the gulf, and the prevalence of seagrass habitat throughout this region supports the view that the demersal eggs of H. melanochir become attached to seagrass and/or algae following spawning. A gyre in waters of the upper gulf, influenced by prevailing southerly winds, the Coriolis effect, and land boundaries, may explain retention of larvae. The importance of seagrass beds to H. melanochir spawning is also supported by anecdotal evidence and available literature on eggs of other Beloniformes, which are also demersal and attach to marine plants. Dual stable isotope analysis (δ¹³ and δ¹⁵N) of larval, juvenile and adult H. melanochir and several potential food sources from the Bay of Shoals was carried out to estimate the importance of zosteracean seagrass towards the assimilated diet of H. melanochir. Although the diet of H. melanochir larvae is probably planktonivorous, their isotopic signatures partly reflect the parental diet due to the influence of pre–existing tissue in addition to growth. According to mixing model calculations, the signatures of juveniles can be explained by a diet consisting of 23–37% Zostera, 0–10% Halophila and the remainder zooplankton, whilst the diet of adults consists of 53–58% Zostera and the remainder zooplankton. These findings indicate an increasing dependence upon Zostera with growth of H. melanochir. The results of this study enhance the completeness of our understanding of the fisheries biology and ecology of H. melanochir. Significant contributions are provided in reproductive biology and larval biology, seagrass beds (in combination with mixed algae) are demonstrated to be an important habitat for spawning, and Zostera seagrass is shown to be a necessary food source in the diet of juveniles and adults. / Thesis (Ph.D.)-- University of Adelaide, School of Earth and Environmental Sciences, 2005.

Title page, contents and abstract only. The complete thesis in print form is available from the University of Adelaide Library. / The aims of this investigation on the Holocene carbonate successions of three shallow, ephemeral lakes from the Cooring coastal plain were: to determine the timing of the sapropel ’events’ in the three lakes; to determine the origin of the sapropelic organic matter and evaluate changes; to establish whether sapropel deposition in these shallow, coastal lakes primarily reflects increased organic matter delivery to the sediments during periods of enhanced terrestrial input and/or aquatic productivity, and; to relate sapropel deposition in these three lakes to both regional and global palaeoenvironment reconstructions. --p. 23-24. / http://proxy.library.adelaide.edu.au/login?url= http://library.adelaide.edu.au/cgi-bin/Pwebrecon.cgi?BBID=1324064 / Thesis (Ph.D.) -- University of Adelaide, School of Earth and Environmental Sciences, 2007

This study investigates early life stages of the southern sea garfish (Hyporhamphus melanochir) and their association with seagrass in Gulf St Vincent, South Australia. The overall aims were to identify and describe the early life stages of H. melanochir and to explore the possible relationship(s) between these life stages and seagrass habitat with the emphasis on seagrass as a requirement for spawning or as a food source. The reproductive biology of female H. melanochir from the commercial fishery was assessed by microscopic examination of ovaries, oocyte size distributions, gonadosomatic indices, and macroscopic ovarian stages. Five stages of oocyte development were identified and described: perinucleolar, yolk vesicle, yolk globule, migratory nucleus and hydrated. A coherence between histological and whole oocyte descriptions is demonstrated. Hyporhamphus melanochir are characterised as multiple spawners with group-synchronous oocyte development and indeterminate fecundity. A protracted spawning season from October to March was indicated by the occurrence of ripe ovaries and increases in gonadosomatic index. Females reach sexual maturity at 193 mm standard length, and batch fecundity ranged from 201-3044 oocytes depending on fish size. Spawning shoals are segregated by sex, as indicated by commercial samples, with a biased female-to-male ratio of 4.5:1 during the spawning season (1.2:1 during the non-spawning season). In addition, features of the oocyte surface were closely examined, which revealed that the filaments on the chorion of the hydrated oocyte are adhesive. These adhesive filaments presumably allow the fertilised egg to become attached to vegetative substrate by adhesion and/or entanglement. H. melanochir larvae were discriminated from another hemiramphid species, river garfish (H. regularis), which is also known to occur in the study area, based on species-specific amplification of part of the mitochondrial control region using a multiplex polymerase chain reaction (PCR) assay. The species were easily discerned by the number and distinct sizes of PCR products [H. melanochir, 443 bp; river garfish (H. regularis), 462 and 264 bp]. Although based on a single gene, this molecular method will correctly identify the species of individuals in at least 96% and 94% of tests for H. melanochir and H. regularis, respectively. Subsequent to verifying the identification of species by molecular discrimination, the larval development of H. melanochir and H. regularis were described. Larvae of H. melanochir and H. regularis had completed notochord flexion at hatching and are characterized by their elongate body with distinct rows of melanophores along the dorsal, lateral and ventral surfaces; small to moderate head; heavily pigmented, long straight gut; persistent preanal finfold; and extended lower jaw. Fin formation occurs in the sequence: caudal, dorsal and anal (almost simultaneously), pectoral, pelvic. Despite the similarities between both species and among hemiramphid larvae in general, H. melanochir larvae are distinguishable from H. regularis by: having 58-61 vertebrae (v. 51-54 for H. regularis); having 12-15 melanophore pairs in longitudinal rows along the dorsal margin between the head and origin of the dorsal fin (v. 19-22 for H. regularis); and the absence of a large ventral pigment blotch anteriorly on the gut and isthmus (present in H. regularis). A logistic regression analysis of body measurements also revealed interspecies differences in the combined measurements of eye diameter and pre-anal fin length. Both species can be distinguished from morphologically similar larvae found in southern Australia (other hemiramphids and a scomberosocid) by differences in meristic counts and pigmentation. Hyporhamphus melanochir larvae were successfully collected throughout Gulf St Vincent using a neuston net; however, attempts to sample eggs were unsuccessful. Abundances of larvae in the gulf averaged 4.8 and 12.3 larvae 1000⁻ ² of surface water in December 1998 and December 2000, respectively. Larvae exhibit fast growth, as indicated by otolith growth increments, with backcalculated spawning dates falling within the October-March spawning season. Spatial analysis of larval distributions revealed a positive spatial autocorrelation, i.e. non-randomness or clustering of similar abundance values. Most larvae were found in the upper region of the gulf, and the prevalence of seagrass habitat throughout this region supports the view that the demersal eggs of H. melanochir become attached to seagrass and/or algae following spawning. A gyre in waters of the upper gulf, influenced by prevailing southerly winds, the Coriolis effect, and land boundaries, may explain retention of larvae. The importance of seagrass beds to H. melanochir spawning is also supported by anecdotal evidence and available literature on eggs of other Beloniformes, which are also demersal and attach to marine plants. Dual stable isotope analysis (δ¹³ and δ¹⁵N) of larval, juvenile and adult H. melanochir and several potential food sources from the Bay of Shoals was carried out to estimate the importance of zosteracean seagrass towards the assimilated diet of H. melanochir. Although the diet of H. melanochir larvae is probably planktonivorous, their isotopic signatures partly reflect the parental diet due to the influence of pre–existing tissue in addition to growth. According to mixing model calculations, the signatures of juveniles can be explained by a diet consisting of 23–37% Zostera, 0–10% Halophila and the remainder zooplankton, whilst the diet of adults consists of 53–58% Zostera and the remainder zooplankton. These findings indicate an increasing dependence upon Zostera with growth of H. melanochir. The results of this study enhance the completeness of our understanding of the fisheries biology and ecology of H. melanochir. Significant contributions are provided in reproductive biology and larval biology, seagrass beds (in combination with mixed algae) are demonstrated to be an important habitat for spawning, and Zostera seagrass is shown to be a necessary food source in the diet of juveniles and adults. / Thesis (Ph.D.)-- University of Adelaide, School of Earth and Environmental Sciences, 2005.

This study investigates early life stages of the southern sea garfish (Hyporhamphus melanochir) and their association with seagrass in Gulf St Vincent, South Australia. The overall aims were to identify and describe the early life stages of H. melanochir and to explore the possible relationship(s) between these life stages and seagrass habitat with the emphasis on seagrass as a requirement for spawning or as a food source. The reproductive biology of female H. melanochir from the commercial fishery was assessed by microscopic examination of ovaries, oocyte size distributions, gonadosomatic indices, and macroscopic ovarian stages. Five stages of oocyte development were identified and described: perinucleolar, yolk vesicle, yolk globule, migratory nucleus and hydrated. A coherence between histological and whole oocyte descriptions is demonstrated. Hyporhamphus melanochir are characterised as multiple spawners with group-synchronous oocyte development and indeterminate fecundity. A protracted spawning season from October to March was indicated by the occurrence of ripe ovaries and increases in gonadosomatic index. Females reach sexual maturity at 193 mm standard length, and batch fecundity ranged from 201-3044 oocytes depending on fish size. Spawning shoals are segregated by sex, as indicated by commercial samples, with a biased female-to-male ratio of 4.5:1 during the spawning season (1.2:1 during the non-spawning season). In addition, features of the oocyte surface were closely examined, which revealed that the filaments on the chorion of the hydrated oocyte are adhesive. These adhesive filaments presumably allow the fertilised egg to become attached to vegetative substrate by adhesion and/or entanglement. H. melanochir larvae were discriminated from another hemiramphid species, river garfish (H. regularis), which is also known to occur in the study area, based on species-specific amplification of part of the mitochondrial control region using a multiplex polymerase chain reaction (PCR) assay. The species were easily discerned by the number and distinct sizes of PCR products [H. melanochir, 443 bp; river garfish (H. regularis), 462 and 264 bp]. Although based on a single gene, this molecular method will correctly identify the species of individuals in at least 96% and 94% of tests for H. melanochir and H. regularis, respectively. Subsequent to verifying the identification of species by molecular discrimination, the larval development of H. melanochir and H. regularis were described. Larvae of H. melanochir and H. regularis had completed notochord flexion at hatching and are characterized by their elongate body with distinct rows of melanophores along the dorsal, lateral and ventral surfaces; small to moderate head; heavily pigmented, long straight gut; persistent preanal finfold; and extended lower jaw. Fin formation occurs in the sequence: caudal, dorsal and anal (almost simultaneously), pectoral, pelvic. Despite the similarities between both species and among hemiramphid larvae in general, H. melanochir larvae are distinguishable from H. regularis by: having 58-61 vertebrae (v. 51-54 for H. regularis); having 12-15 melanophore pairs in longitudinal rows along the dorsal margin between the head and origin of the dorsal fin (v. 19-22 for H. regularis); and the absence of a large ventral pigment blotch anteriorly on the gut and isthmus (present in H. regularis). A logistic regression analysis of body measurements also revealed interspecies differences in the combined measurements of eye diameter and pre-anal fin length. Both species can be distinguished from morphologically similar larvae found in southern Australia (other hemiramphids and a scomberosocid) by differences in meristic counts and pigmentation. Hyporhamphus melanochir larvae were successfully collected throughout Gulf St Vincent using a neuston net; however, attempts to sample eggs were unsuccessful. Abundances of larvae in the gulf averaged 4.8 and 12.3 larvae 1000⁻ ² of surface water in December 1998 and December 2000, respectively. Larvae exhibit fast growth, as indicated by otolith growth increments, with backcalculated spawning dates falling within the October-March spawning season. Spatial analysis of larval distributions revealed a positive spatial autocorrelation, i.e. non-randomness or clustering of similar abundance values. Most larvae were found in the upper region of the gulf, and the prevalence of seagrass habitat throughout this region supports the view that the demersal eggs of H. melanochir become attached to seagrass and/or algae following spawning. A gyre in waters of the upper gulf, influenced by prevailing southerly winds, the Coriolis effect, and land boundaries, may explain retention of larvae. The importance of seagrass beds to H. melanochir spawning is also supported by anecdotal evidence and available literature on eggs of other Beloniformes, which are also demersal and attach to marine plants. Dual stable isotope analysis (δ¹³ and δ¹⁵N) of larval, juvenile and adult H. melanochir and several potential food sources from the Bay of Shoals was carried out to estimate the importance of zosteracean seagrass towards the assimilated diet of H. melanochir. Although the diet of H. melanochir larvae is probably planktonivorous, their isotopic signatures partly reflect the parental diet due to the influence of pre–existing tissue in addition to growth. According to mixing model calculations, the signatures of juveniles can be explained by a diet consisting of 23–37% Zostera, 0–10% Halophila and the remainder zooplankton, whilst the diet of adults consists of 53–58% Zostera and the remainder zooplankton. These findings indicate an increasing dependence upon Zostera with growth of H. melanochir. The results of this study enhance the completeness of our understanding of the fisheries biology and ecology of H. melanochir. Significant contributions are provided in reproductive biology and larval biology, seagrass beds (in combination with mixed algae) are demonstrated to be an important habitat for spawning, and Zostera seagrass is shown to be a necessary food source in the diet of juveniles and adults. / Thesis (Ph.D.)-- University of Adelaide, School of Earth and Environmental Sciences, 2005.

Thesis (M.A.)--University of Adelaide, 1984. / Includes bibliographical references (p. 208-221).

Thesis (Ph. D.)--University of Adelaide, 1989. / Typescript (Photocopy). Includes bibliographical references (leaves 305-319).

Thesis (B.A. (Hons.))--University of Adelaide, 1978. / Includes bibliographical references (leaf 97-102).