The acanthodians were a common and widespread group of fishes throughout the world during the mid-Palaeozoic. In this study, a full-scale systematic analysis of Silurian to Middle Devonian acanthodian taxa of eastern Australia was undertaken, incorporating a review and updating of historical records and descriptions of taxa. Phylogenetic relationships within the group and with other early gnathostomes are uncertain. The structure, function and modes of growth of acanthodian scales were described and investigated, and these features were used for comparisons between different taxa within the group, and between acanthodians and other early vertebrates. Histological and morphological characters of the scales were incorporated in a cladistic analysis of genera erected for articulated fish. This analysis did not support the traditional ordinal level groups, the Climatiida, Ischnacanthida and Acanthodida. Therefore, the highest taxonomic level used in the study was the family. Rarely were acanthodians preserved as articulated fossils. The only examples known from the Silurian-Middle Devonian of Australia are one specimen of the putative acanthodian Yealepis douglasi Burrow & Young 1999 from the Ludlow of Victoria, five specimens of an indeterminate ?ischnacanthidid from the late Givetian of New South Wales and a rich assemblage from the Givetian lacustrine shales of Mt Howitt, Victoria. The latter fauna (originally dated as Late Devonian) includes six incomplete specimens of the culmacanthidid Culmacanthus stewarti Long 1983 and about 60 specimens of acanthodidid Howittacanthus kentoni Long 1986. In contrast, disassociated remains of the group are ubiquitous in microvertebrate faunas from the mid-Palaeozoic of eastern Australia. Although scales of other fish groups are sometimes more common in particular facies, acanthodian elements are found in all depositional environments, from deep shelf marine to transitional to freshwater. Most of the taxa, particularly those only preserved as isolated scales, had not been systematically described by other workers. This thesis incorporates descriptions of new taxa, and revision and updating of other taxa. Several overseas studies have produced biostratigraphic charts based on acanthodian scales. A similar biostratigraphic overview was undertaken based on a systematic analysis of the Early Devonian acanthodians of eastern Australia, permitting comparisons with acanthodian faunas of other regions. Acanthodian scales and fin spines are the most common elements in the few vertebrate faunas that are known from the Silurian of Australia. Diversity and geographic distribution of the acanthodian faunas peaked during the Early Devonian. This study has been hampered by the low numbers of scales in many samples, and by uncertainty over their dating (particularly for the faunas from non-limestone deposits). Nevertheless, the work shows that changes in the marine assemblages are broadly correlated with the pattern of marine transgressions and regressions. Composition of the acanthodian faunas, and their abundance relative to other vertebrates in the assemblages, depend on the depositional environment. This correlation is best illustrated in Lower Devonian deposits, in which acanthodians are the most prolific and diverse. In transitional and marginal marine deposits, thelodonts are dominant, and acanthodians a minor element of the fauna. In off-shore assemblages, acanthodians and placoderms are dominant, and thelodonts are rare or absent. Vertebrate faunas are poor in the earliest Devonian deposits, but become more common by the late Lochkovian, with near-shore assemblages characterized by Trundlelepis cervicostulata and ANostolepis@ guangxiensis, and deeper shelf assemblages by a new genus, possibly assignable to the Ischnacanthidae. The vertebrate record is sparse through the middle Pragian, though AN.@ guangxiensis is present low in the Coopers Creek Limestone (upper sulcatus-pireneae zones), being replaced by Nostolepoides platymarginata, Gomphonchus? bogongensis, and Radioporacanthodes sp. aff. R. (Gomphonchus) liujingensis by the kindlei Zone. Microvertebrate assemblages are more common by the late Pragian (pireneae Zone), with Radioporacanthodes sp. aff. R. liujingensis in deeper shelf deposits, and N. platymarginata and G.? bogongensis dominating near-shore assemblages. The earliest Emsian (dehiscens Zone) is marked by the incoming Cheiracanthoides wangi. Middle Emsian (perbonus-serotinus zones) assemblages are characterized by two new species, possibly assignable to Gomphonchus.The Middle Devonian cosmopolitan association of Cheiracanthoides comptus and AAcanthoides@ dublinensis, which characterizes early Middle Devonian faunas from North America, Europe and China, appears first in the latest Emsian at the serotinus-patulus zone boundary. As well as showing the value of acanthodians in biostratigraphy and as indicators of environmental settings, their use in biogeography was demonstrated. Although many of the acanthodian taxa are endemic, several are also found in other regions. The Silurian to earliest Devonian faunas of eastern Australia are most closely related to coeval Chinese assemblages. Several latest Silurian-earliest Devonian taxa are also recorded from the circum-Arctic region. The late Lochkovian to early Emsian assemblages, particularly from south-eastern Australia, have many taxa in common with Chinese faunas. The mid-Emsian taxa show highest endemicity; and the latest Emsian-Eifelian assemblages have the most cosmopolitan aspect. Acanthodian faunas become rarer and depauperate in the Middle Devonian, particularly in the south-eastern corner, and are mostly in poorly dated, ?fluviatile/marginal marine deposits. This study of acanthodian faunas has encompassed a full scale systematic review of the group in this region, an appraisal of phylogenetic relationships within the group and with other early vertebrates, their palaeoecology, and their use in biostratigraphy and biogeography.

The acanthodians were a common and widespread group of fishes throughout the world during the mid-Palaeozoic. In this study, a full-scale systematic analysis of Silurian to Middle Devonian acanthodian taxa of eastern Australia was undertaken, incorporating a review and updating of historical records and descriptions of taxa. Phylogenetic relationships within the group and with other early gnathostomes are uncertain. The structure, function and modes of growth of acanthodian scales were described and investigated, and these features were used for comparisons between different taxa within the group, and between acanthodians and other early vertebrates. Histological and morphological characters of the scales were incorporated in a cladistic analysis of genera erected for articulated fish. This analysis did not support the traditional ordinal level groups, the Climatiida, Ischnacanthida and Acanthodida. Therefore, the highest taxonomic level used in the study was the family. Rarely were acanthodians preserved as articulated fossils. The only examples known from the Silurian-Middle Devonian of Australia are one specimen of the putative acanthodian Yealepis douglasi Burrow & Young 1999 from the Ludlow of Victoria, five specimens of an indeterminate ?ischnacanthidid from the late Givetian of New South Wales and a rich assemblage from the Givetian lacustrine shales of Mt Howitt, Victoria. The latter fauna (originally dated as Late Devonian) includes six incomplete specimens of the culmacanthidid Culmacanthus stewarti Long 1983 and about 60 specimens of acanthodidid Howittacanthus kentoni Long 1986. In contrast, disassociated remains of the group are ubiquitous in microvertebrate faunas from the mid-Palaeozoic of eastern Australia. Although scales of other fish groups are sometimes more common in particular facies, acanthodian elements are found in all depositional environments, from deep shelf marine to transitional to freshwater. Most of the taxa, particularly those only preserved as isolated scales, had not been systematically described by other workers. This thesis incorporates descriptions of new taxa, and revision and updating of other taxa. Several overseas studies have produced biostratigraphic charts based on acanthodian scales. A similar biostratigraphic overview was undertaken based on a systematic analysis of the Early Devonian acanthodians of eastern Australia, permitting comparisons with acanthodian faunas of other regions. Acanthodian scales and fin spines are the most common elements in the few vertebrate faunas that are known from the Silurian of Australia. Diversity and geographic distribution of the acanthodian faunas peaked during the Early Devonian. This study has been hampered by the low numbers of scales in many samples, and by uncertainty over their dating (particularly for the faunas from non-limestone deposits). Nevertheless, the work shows that changes in the marine assemblages are broadly correlated with the pattern of marine transgressions and regressions. Composition of the acanthodian faunas, and their abundance relative to other vertebrates in the assemblages, depend on the depositional environment. This correlation is best illustrated in Lower Devonian deposits, in which acanthodians are the most prolific and diverse. In transitional and marginal marine deposits, thelodonts are dominant, and acanthodians a minor element of the fauna. In off-shore assemblages, acanthodians and placoderms are dominant, and thelodonts are rare or absent. Vertebrate faunas are poor in the earliest Devonian deposits, but become more common by the late Lochkovian, with near-shore assemblages characterized by Trundlelepis cervicostulata and ANostolepis@ guangxiensis, and deeper shelf assemblages by a new genus, possibly assignable to the Ischnacanthidae. The vertebrate record is sparse through the middle Pragian, though AN.@ guangxiensis is present low in the Coopers Creek Limestone (upper sulcatus-pireneae zones), being replaced by Nostolepoides platymarginata, Gomphonchus? bogongensis, and Radioporacanthodes sp. aff. R. (Gomphonchus) liujingensis by the kindlei Zone. Microvertebrate assemblages are more common by the late Pragian (pireneae Zone), with Radioporacanthodes sp. aff. R. liujingensis in deeper shelf deposits, and N. platymarginata and G.? bogongensis dominating near-shore assemblages. The earliest Emsian (dehiscens Zone) is marked by the incoming Cheiracanthoides wangi. Middle Emsian (perbonus-serotinus zones) assemblages are characterized by two new species, possibly assignable to Gomphonchus.The Middle Devonian cosmopolitan association of Cheiracanthoides comptus and AAcanthoides@ dublinensis, which characterizes early Middle Devonian faunas from North America, Europe and China, appears first in the latest Emsian at the serotinus-patulus zone boundary. As well as showing the value of acanthodians in biostratigraphy and as indicators of environmental settings, their use in biogeography was demonstrated. Although many of the acanthodian taxa are endemic, several are also found in other regions. The Silurian to earliest Devonian faunas of eastern Australia are most closely related to coeval Chinese assemblages. Several latest Silurian-earliest Devonian taxa are also recorded from the circum-Arctic region. The late Lochkovian to early Emsian assemblages, particularly from south-eastern Australia, have many taxa in common with Chinese faunas. The mid-Emsian taxa show highest endemicity; and the latest Emsian-Eifelian assemblages have the most cosmopolitan aspect. Acanthodian faunas become rarer and depauperate in the Middle Devonian, particularly in the south-eastern corner, and are mostly in poorly dated, ?fluviatile/marginal marine deposits. This study of acanthodian faunas has encompassed a full scale systematic review of the group in this region, an appraisal of phylogenetic relationships within the group and with other early vertebrates, their palaeoecology, and their use in biostratigraphy and biogeography.

<p>The Superfamily Strophomenoidea is a very diverse group of brachiopods in the Early Palaeozoic. In the Silurian succession on Gotland, they are among the most easily identifiable, and commonly found fossils. However, there are few detailed studies of this group from Gotland, and no new strophomenide taxa have been described from this area since 1869. The life habits of strophomenides are also poorly understood, partly because their morphology differs greatly from that of living brachiopods. </p><p>The succession on Gotland yielded 27 species belonging to the Strophomenoidea, of which two species and two subspecies are new. The remaining species have been described earlier from Gotland or Great Britain. The most important group is the Leptaeninae, which occurs commonly throughout the entire succession on Gotland. Five species (one new), two new subspecies and two taxa treated under open nomenclature were found. <i>Leptaena rhomboidalis</i> and <i>Lepidoleptaena poulseni</i> were specialized for life in shallow water environments, retaining a large apical pedicle; the remaining leptaenines were ambitopic. The Furcitellininae is represented by three genera comprising six species, of which only one persisted into the Ludlow. All were ambitopic, except <i>Pentlandina loveni</i>, which was specialized for high-energy environments. Six species of “strophodontids” from Gotland, belonging to the Leptostrophidae, the Strophodontidae and the Shaleriidae, share a shallow-bodied, variably concavo-convex shell with costellate ornament. <i>Mesoleptostrophia</i> and <i>Brachyprion</i> (<i>Brachyprion</i>) were long-ranged and ecologically tolerant, while <i>B.</i> (<i>Erinostrophia</i>), <i>Strophodonta</i> and <i>Shaleria</i> had short ranges and were ecologically specialized. The two earliest known cementing strophomenides occur on Gotland, and their hitherto unknown dorsal valves have been identified: <i>Liljevallia </i>was found to belong to the Douvillinidae. The cementing <i>Leptaenoidea silurica</i> was found to be conspecific with the ambitopic <i>Scamnomena rugata</i>; it was able to live ambitopically if removed from the substrate. The thickened dorsal valves allow reconstruction of its lophophore.</p>

The Superfamily Strophomenoidea is a very diverse group of brachiopods in the Early Palaeozoic. In the Silurian succession on Gotland, they are among the most easily identifiable, and commonly found fossils. However, there are few detailed studies of this group from Gotland, and no new strophomenide taxa have been described from this area since 1869. The life habits of strophomenides are also poorly understood, partly because their morphology differs greatly from that of living brachiopods. The succession on Gotland yielded 27 species belonging to the Strophomenoidea, of which two species and two subspecies are new. The remaining species have been described earlier from Gotland or Great Britain. The most important group is the Leptaeninae, which occurs commonly throughout the entire succession on Gotland. Five species (one new), two new subspecies and two taxa treated under open nomenclature were found. Leptaena rhomboidalis and Lepidoleptaena poulseni were specialized for life in shallow water environments, retaining a large apical pedicle; the remaining leptaenines were ambitopic. The Furcitellininae is represented by three genera comprising six species, of which only one persisted into the Ludlow. All were ambitopic, except Pentlandina loveni, which was specialized for high-energy environments. Six species of “strophodontids” from Gotland, belonging to the Leptostrophidae, the Strophodontidae and the Shaleriidae, share a shallow-bodied, variably concavo-convex shell with costellate ornament. Mesoleptostrophia and Brachyprion (Brachyprion) were long-ranged and ecologically tolerant, while B. (Erinostrophia), Strophodonta and Shaleria had short ranges and were ecologically specialized. The two earliest known cementing strophomenides occur on Gotland, and their hitherto unknown dorsal valves have been identified: Liljevallia was found to belong to the Douvillinidae. The cementing Leptaenoidea silurica was found to be conspecific with the ambitopic Scamnomena rugata; it was able to live ambitopically if removed from the substrate. The thickened dorsal valves allow reconstruction of its lophophore.

Sedimentary dikes at the Pipe Creek Junior Quarry were found to fill fractures formed by compaction and rotation of the reef flank beds and by regional stresses of less certain origin. A sequence of fracturing events has been established as well as a sequence for the emplacement of dike materials. Most of the carbonate dikes are found to be of Cayugan (Silurian) age, although some of the las carbonates are shown to be of Devonian age due to the presence of rounded detrital quartz grains within them. All of the quartz arenite dikes are found to be of Devonian age and are divided into two major groups: older white arenites and younger brown arenites. The two types of arenties have different characteristics and were deposited under different conditions.The arenites of Pipe Creek Junior Quarry were found to be similar to the arenites of the Bluffton Quarry which are also fracture fillings in Silurian reef rock. Other Devonian sand bodies are compared to the fracture filling and, although they are not identical, they show a similarity in materials and a pattern of environment and deposition that point to a northwestern source for all of the rounded quartz studied in this work. Environmental analysis of the quartz grains indicates a litoral mode of transport and sorting for most of the samples with an ecolian mode present in the sands outside the reef area and as a minor component for some of the younger sands within the reef area.A map of the glaciated quarry surface has been prepared for the purposes of this work and to preserve relationships that are constantly being removed by quarrying of the reef flank beds.

Early gnathostome evolution has recently undergone revision due to newly published phylogenies. Within this new framework, early gnathostomes in the fossil record can be revised, particularly the subject of this paper Tylodus deltoides (Rohon, 1893), vertebrate microremains from the Silurian Ohesaare Formation of Estonia. Multiple analytical approaches are performed in order to offer insight into a phylogenetic position for the enigmatic T. deltoides. A three-dimensional model, based on synchrotron x-ray phase contrast microtomography of a small polyodontode morphotype and virtual thin sections show a unique palaeohistology. A survey of wear patterns shows the presence of tooth plates, comprising the larger cusp and plate morphotypes. Histological observations show a mosaic of vertebrate hard-tissues and organisations, including a tripartitie layered structure, descending rows of odontodes on a large primary odontode, an osteodentine or mesodentine base, pleromic dentine middle layer and capping layer of unknown tissue type.Two interpretations of this collection of observations are given. Both assume the large morphotypes are teeth, one that the smaller polyodontodes are scales, the other, that they are developing teeth. Histology alone demonstrates the remains are the teeth of a holocephalan, but with some uncertainty. A model for attachment by acrodonty and developmental model for conserved lyodont development are given to help explain the unusual histology and morphology of T. deltoides, but greater certainty in the phylogenetic position of T. deltoides requires a more detailed histological analysis based on thin sections and a broader comparison with 3D data of relevent taxa. This willnecessarily be improved by formal phylogenetic analysis. / De käkförsedda ryggradsdjurerens (gnathostomernas) uppkomst och tidiga evolution är ett forsknings-område där nya fossila fynd och paleontologiska forskningsinsatser på senare tid har medfört en bättre övergripande förståelse. Gnathostomerna kan delas in i två grupper: chondrichthyider (broskfiskar så som haja och rockor) och osteichthyider (s.k. benfiskar från vilket landlevande ryggradsdjur också har sitt ursprung). En utdöd grupp av fiskar, de s.k. taggpansarhajarna (acanthoder), har på senare tid ansetts representera de former från vilken broskfiskarna har sitt ursprung. Detta har medfört ett nytt perspektiv till vilket paleontologer måste relatera när de studerar de fossila gnathostomerna och dess tidiga utveckling. Dessutom bidrar även nya tekniker, så som högupplöst skiktröntgen av fossil med hjälp av synkrotronstrålning, till vår förståelse. Dessa tekniker kan ge oss detaljerade tredimensionella modeller av den inre konstruktionen utan att behöva skada de ofta sällsynta fossil som finns till- gängligaDetta arbete avhandlar ett enigmatiskt fiskfossil, Tylodus deltoides, som endast är känt från mer eller mindre mikroskopiska vertebratrester. Dessa fossil beskrevs för första gången så tidigt som 1893, men man har fortfarande inte har lyckat komma fram till var bland ryggradsdjuren dessa hör. Med hjälp av nämnda tekniker och nya perspektiv, är målet med denna studie att ge en ny beskrivning och tolkning av dessa ganska udda fossila rester. Genom att studera skrapmärken på ytan av de individu- ella fossilen så har jag kunna konstatera att åtminstone de större exemplaren är fungerande tänder, medan de mindre troligen är tänder under utveckling och som ännu inte brutit igenom huden i munnen. Genom att via högupplöst skiktröntgen skapa och studera en tredimensionell modell av den inre strukturen så har jag dessutom kommit fram till att dessa tänder troligen hör hemma bland en tidig grupp av broskfiskar som vi kallar helhuvudfiskar (Holocephali). Denna tolkning är inte helt utan problem, men innan man kan komma till mer slutgiltiga slutsatser måste kompletterande studier göras som innefattar jämförbara tredimensionella modeller av andra levande och fossila grupper, samt att med  hjälp  av  dessa  nya  data  även  inkludera  T.  deltoides  i  en  större  analys  rörande  släktskaps-förhållanden.

No description available.

The acanthodians were a common and widespread group of fishes throughout the world during the mid-Palaeozoic. In this study, a full-scale systematic analysis of Silurian to Middle Devonian acanthodian taxa of eastern Australia was undertaken, incorporating a review and updating of historical records and descriptions of taxa. Phylogenetic relationships within the group and with other early gnathostomes are uncertain. The structure, function and modes of growth of acanthodian scales were described and investigated, and these features were used for comparisons between different taxa within the group, and between acanthodians and other early vertebrates. Histological and morphological characters of the scales were incorporated in a cladistic analysis of genera erected for articulated fish. This analysis did not support the traditional ordinal level groups, the Climatiida, Ischnacanthida and Acanthodida. Therefore, the highest taxonomic level used in the study was the family. Rarely were acanthodians preserved as articulated fossils. The only examples known from the Silurian-Middle Devonian of Australia are one specimen of the putative acanthodian Yealepis douglasi Burrow & Young 1999 from the Ludlow of Victoria, five specimens of an indeterminate ?ischnacanthidid from the late Givetian of New South Wales and a rich assemblage from the Givetian lacustrine shales of Mt Howitt, Victoria. The latter fauna (originally dated as Late Devonian) includes six incomplete specimens of the culmacanthidid Culmacanthus stewarti Long 1983 and about 60 specimens of acanthodidid Howittacanthus kentoni Long 1986. In contrast, disassociated remains of the group are ubiquitous in microvertebrate faunas from the mid-Palaeozoic of eastern Australia. Although scales of other fish groups are sometimes more common in particular facies, acanthodian elements are found in all depositional environments, from deep shelf marine to transitional to freshwater. Most of the taxa, particularly those only preserved as isolated scales, had not been systematically described by other workers. This thesis incorporates descriptions of new taxa, and revision and updating of other taxa. Several overseas studies have produced biostratigraphic charts based on acanthodian scales. A similar biostratigraphic overview was undertaken based on a systematic analysis of the Early Devonian acanthodians of eastern Australia, permitting comparisons with acanthodian faunas of other regions. Acanthodian scales and fin spines are the most common elements in the few vertebrate faunas that are known from the Silurian of Australia. Diversity and geographic distribution of the acanthodian faunas peaked during the Early Devonian. This study has been hampered by the low numbers of scales in many samples, and by uncertainty over their dating (particularly for the faunas from non-limestone deposits). Nevertheless, the work shows that changes in the marine assemblages are broadly correlated with the pattern of marine transgressions and regressions. Composition of the acanthodian faunas, and their abundance relative to other vertebrates in the assemblages, depend on the depositional environment. This correlation is best illustrated in Lower Devonian deposits, in which acanthodians are the most prolific and diverse. In transitional and marginal marine deposits, thelodonts are dominant, and acanthodians a minor element of the fauna. In off-shore assemblages, acanthodians and placoderms are dominant, and thelodonts are rare or absent. Vertebrate faunas are poor in the earliest Devonian deposits, but become more common by the late Lochkovian, with near-shore assemblages characterized by Trundlelepis cervicostulata and ANostolepis@ guangxiensis, and deeper shelf assemblages by a new genus, possibly assignable to the Ischnacanthidae. The vertebrate record is sparse through the middle Pragian, though AN.@ guangxiensis is present low in the Coopers Creek Limestone (upper sulcatus-pireneae zones), being replaced by Nostolepoides platymarginata, Gomphonchus? bogongensis, and Radioporacanthodes sp. aff. R. (Gomphonchus) liujingensis by the kindlei Zone. Microvertebrate assemblages are more common by the late Pragian (pireneae Zone), with Radioporacanthodes sp. aff. R. liujingensis in deeper shelf deposits, and N. platymarginata and G.? bogongensis dominating near-shore assemblages. The earliest Emsian (dehiscens Zone) is marked by the incoming Cheiracanthoides wangi. Middle Emsian (perbonus-serotinus zones) assemblages are characterized by two new species, possibly assignable to Gomphonchus.The Middle Devonian cosmopolitan association of Cheiracanthoides comptus and AAcanthoides@ dublinensis, which characterizes early Middle Devonian faunas from North America, Europe and China, appears first in the latest Emsian at the serotinus-patulus zone boundary. As well as showing the value of acanthodians in biostratigraphy and as indicators of environmental settings, their use in biogeography was demonstrated. Although many of the acanthodian taxa are endemic, several are also found in other regions. The Silurian to earliest Devonian faunas of eastern Australia are most closely related to coeval Chinese assemblages. Several latest Silurian-earliest Devonian taxa are also recorded from the circum-Arctic region. The late Lochkovian to early Emsian assemblages, particularly from south-eastern Australia, have many taxa in common with Chinese faunas. The mid-Emsian taxa show highest endemicity; and the latest Emsian-Eifelian assemblages have the most cosmopolitan aspect. Acanthodian faunas become rarer and depauperate in the Middle Devonian, particularly in the south-eastern corner, and are mostly in poorly dated, ?fluviatile/marginal marine deposits. This study of acanthodian faunas has encompassed a full scale systematic review of the group in this region, an appraisal of phylogenetic relationships within the group and with other early vertebrates, their palaeoecology, and their use in biostratigraphy and biogeography.

The acanthodians were a common and widespread group of fishes throughout the world during the mid-Palaeozoic. In this study, a full-scale systematic analysis of Silurian to Middle Devonian acanthodian taxa of eastern Australia was undertaken, incorporating a review and updating of historical records and descriptions of taxa. Phylogenetic relationships within the group and with other early gnathostomes are uncertain. The structure, function and modes of growth of acanthodian scales were described and investigated, and these features were used for comparisons between different taxa within the group, and between acanthodians and other early vertebrates. Histological and morphological characters of the scales were incorporated in a cladistic analysis of genera erected for articulated fish. This analysis did not support the traditional ordinal level groups, the Climatiida, Ischnacanthida and Acanthodida. Therefore, the highest taxonomic level used in the study was the family. Rarely were acanthodians preserved as articulated fossils. The only examples known from the Silurian-Middle Devonian of Australia are one specimen of the putative acanthodian Yealepis douglasi Burrow & Young 1999 from the Ludlow of Victoria, five specimens of an indeterminate ?ischnacanthidid from the late Givetian of New South Wales and a rich assemblage from the Givetian lacustrine shales of Mt Howitt, Victoria. The latter fauna (originally dated as Late Devonian) includes six incomplete specimens of the culmacanthidid Culmacanthus stewarti Long 1983 and about 60 specimens of acanthodidid Howittacanthus kentoni Long 1986. In contrast, disassociated remains of the group are ubiquitous in microvertebrate faunas from the mid-Palaeozoic of eastern Australia. Although scales of other fish groups are sometimes more common in particular facies, acanthodian elements are found in all depositional environments, from deep shelf marine to transitional to freshwater. Most of the taxa, particularly those only preserved as isolated scales, had not been systematically described by other workers. This thesis incorporates descriptions of new taxa, and revision and updating of other taxa. Several overseas studies have produced biostratigraphic charts based on acanthodian scales. A similar biostratigraphic overview was undertaken based on a systematic analysis of the Early Devonian acanthodians of eastern Australia, permitting comparisons with acanthodian faunas of other regions. Acanthodian scales and fin spines are the most common elements in the few vertebrate faunas that are known from the Silurian of Australia. Diversity and geographic distribution of the acanthodian faunas peaked during the Early Devonian. This study has been hampered by the low numbers of scales in many samples, and by uncertainty over their dating (particularly for the faunas from non-limestone deposits). Nevertheless, the work shows that changes in the marine assemblages are broadly correlated with the pattern of marine transgressions and regressions. Composition of the acanthodian faunas, and their abundance relative to other vertebrates in the assemblages, depend on the depositional environment. This correlation is best illustrated in Lower Devonian deposits, in which acanthodians are the most prolific and diverse. In transitional and marginal marine deposits, thelodonts are dominant, and acanthodians a minor element of the fauna. In off-shore assemblages, acanthodians and placoderms are dominant, and thelodonts are rare or absent. Vertebrate faunas are poor in the earliest Devonian deposits, but become more common by the late Lochkovian, with near-shore assemblages characterized by Trundlelepis cervicostulata and ANostolepis@ guangxiensis, and deeper shelf assemblages by a new genus, possibly assignable to the Ischnacanthidae. The vertebrate record is sparse through the middle Pragian, though AN.@ guangxiensis is present low in the Coopers Creek Limestone (upper sulcatus-pireneae zones), being replaced by Nostolepoides platymarginata, Gomphonchus? bogongensis, and Radioporacanthodes sp. aff. R. (Gomphonchus) liujingensis by the kindlei Zone. Microvertebrate assemblages are more common by the late Pragian (pireneae Zone), with Radioporacanthodes sp. aff. R. liujingensis in deeper shelf deposits, and N. platymarginata and G.? bogongensis dominating near-shore assemblages. The earliest Emsian (dehiscens Zone) is marked by the incoming Cheiracanthoides wangi. Middle Emsian (perbonus-serotinus zones) assemblages are characterized by two new species, possibly assignable to Gomphonchus.The Middle Devonian cosmopolitan association of Cheiracanthoides comptus and AAcanthoides@ dublinensis, which characterizes early Middle Devonian faunas from North America, Europe and China, appears first in the latest Emsian at the serotinus-patulus zone boundary. As well as showing the value of acanthodians in biostratigraphy and as indicators of environmental settings, their use in biogeography was demonstrated. Although many of the acanthodian taxa are endemic, several are also found in other regions. The Silurian to earliest Devonian faunas of eastern Australia are most closely related to coeval Chinese assemblages. Several latest Silurian-earliest Devonian taxa are also recorded from the circum-Arctic region. The late Lochkovian to early Emsian assemblages, particularly from south-eastern Australia, have many taxa in common with Chinese faunas. The mid-Emsian taxa show highest endemicity; and the latest Emsian-Eifelian assemblages have the most cosmopolitan aspect. Acanthodian faunas become rarer and depauperate in the Middle Devonian, particularly in the south-eastern corner, and are mostly in poorly dated, ?fluviatile/marginal marine deposits. This study of acanthodian faunas has encompassed a full scale systematic review of the group in this region, an appraisal of phylogenetic relationships within the group and with other early vertebrates, their palaeoecology, and their use in biostratigraphy and biogeography.

The acanthodians were a common and widespread group of fishes throughout the world during the mid-Palaeozoic. In this study, a full-scale systematic analysis of Silurian to Middle Devonian acanthodian taxa of eastern Australia was undertaken, incorporating a review and updating of historical records and descriptions of taxa. Phylogenetic relationships within the group and with other early gnathostomes are uncertain. The structure, function and modes of growth of acanthodian scales were described and investigated, and these features were used for comparisons between different taxa within the group, and between acanthodians and other early vertebrates. Histological and morphological characters of the scales were incorporated in a cladistic analysis of genera erected for articulated fish. This analysis did not support the traditional ordinal level groups, the Climatiida, Ischnacanthida and Acanthodida. Therefore, the highest taxonomic level used in the study was the family. Rarely were acanthodians preserved as articulated fossils. The only examples known from the Silurian-Middle Devonian of Australia are one specimen of the putative acanthodian Yealepis douglasi Burrow & Young 1999 from the Ludlow of Victoria, five specimens of an indeterminate ?ischnacanthidid from the late Givetian of New South Wales and a rich assemblage from the Givetian lacustrine shales of Mt Howitt, Victoria. The latter fauna (originally dated as Late Devonian) includes six incomplete specimens of the culmacanthidid Culmacanthus stewarti Long 1983 and about 60 specimens of acanthodidid Howittacanthus kentoni Long 1986. In contrast, disassociated remains of the group are ubiquitous in microvertebrate faunas from the mid-Palaeozoic of eastern Australia. Although scales of other fish groups are sometimes more common in particular facies, acanthodian elements are found in all depositional environments, from deep shelf marine to transitional to freshwater. Most of the taxa, particularly those only preserved as isolated scales, had not been systematically described by other workers. This thesis incorporates descriptions of new taxa, and revision and updating of other taxa. Several overseas studies have produced biostratigraphic charts based on acanthodian scales. A similar biostratigraphic overview was undertaken based on a systematic analysis of the Early Devonian acanthodians of eastern Australia, permitting comparisons with acanthodian faunas of other regions. Acanthodian scales and fin spines are the most common elements in the few vertebrate faunas that are known from the Silurian of Australia. Diversity and geographic distribution of the acanthodian faunas peaked during the Early Devonian. This study has been hampered by the low numbers of scales in many samples, and by uncertainty over their dating (particularly for the faunas from non-limestone deposits). Nevertheless, the work shows that changes in the marine assemblages are broadly correlated with the pattern of marine transgressions and regressions. Composition of the acanthodian faunas, and their abundance relative to other vertebrates in the assemblages, depend on the depositional environment. This correlation is best illustrated in Lower Devonian deposits, in which acanthodians are the most prolific and diverse. In transitional and marginal marine deposits, thelodonts are dominant, and acanthodians a minor element of the fauna. In off-shore assemblages, acanthodians and placoderms are dominant, and thelodonts are rare or absent. Vertebrate faunas are poor in the earliest Devonian deposits, but become more common by the late Lochkovian, with near-shore assemblages characterized by Trundlelepis cervicostulata and ANostolepis@ guangxiensis, and deeper shelf assemblages by a new genus, possibly assignable to the Ischnacanthidae. The vertebrate record is sparse through the middle Pragian, though AN.@ guangxiensis is present low in the Coopers Creek Limestone (upper sulcatus-pireneae zones), being replaced by Nostolepoides platymarginata, Gomphonchus? bogongensis, and Radioporacanthodes sp. aff. R. (Gomphonchus) liujingensis by the kindlei Zone. Microvertebrate assemblages are more common by the late Pragian (pireneae Zone), with Radioporacanthodes sp. aff. R. liujingensis in deeper shelf deposits, and N. platymarginata and G.? bogongensis dominating near-shore assemblages. The earliest Emsian (dehiscens Zone) is marked by the incoming Cheiracanthoides wangi. Middle Emsian (perbonus-serotinus zones) assemblages are characterized by two new species, possibly assignable to Gomphonchus.The Middle Devonian cosmopolitan association of Cheiracanthoides comptus and AAcanthoides@ dublinensis, which characterizes early Middle Devonian faunas from North America, Europe and China, appears first in the latest Emsian at the serotinus-patulus zone boundary. As well as showing the value of acanthodians in biostratigraphy and as indicators of environmental settings, their use in biogeography was demonstrated. Although many of the acanthodian taxa are endemic, several are also found in other regions. The Silurian to earliest Devonian faunas of eastern Australia are most closely related to coeval Chinese assemblages. Several latest Silurian-earliest Devonian taxa are also recorded from the circum-Arctic region. The late Lochkovian to early Emsian assemblages, particularly from south-eastern Australia, have many taxa in common with Chinese faunas. The mid-Emsian taxa show highest endemicity; and the latest Emsian-Eifelian assemblages have the most cosmopolitan aspect. Acanthodian faunas become rarer and depauperate in the Middle Devonian, particularly in the south-eastern corner, and are mostly in poorly dated, ?fluviatile/marginal marine deposits. This study of acanthodian faunas has encompassed a full scale systematic review of the group in this region, an appraisal of phylogenetic relationships within the group and with other early vertebrates, their palaeoecology, and their use in biostratigraphy and biogeography.