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A large enigmatic fossil is described from the early Cambrian (Series 2, Stage 3) Heatherdale Shale in the Fleurieu Peninsula, South Australia. It has an almost circular outline about 150 mm across, with an outer rim and 27-30 evenly-spaced rays that extend about two-thirds of the distance to the centre of the structure; it shows radial symmetry. There is a featureless central area with a width about one-third that of the entire specimen. The fossil is preserved as pale-coloured material that stands out slightly above the surrounding mudstone. XRF data indicate that there is little compositional difference between the fossil and the enclosing rock. The fossil may appear to be a transverse section of a larger organism, but it does not continue down into the surrounding rock. This suggests it is a non-mineralised compression fossil that retains the remnants of a three-dimensional structure. Possible affinities with radiodont oral cones, ctenophores, eldonioids, scyphozoa and archaeocyaths are discussed, but no definite assignment can be made. Refereed/Peer-reviewed

Studies that reveal detailed information about trilobite growth, particularly early developmental stages, are crucial for improving our understanding of the phylogenetic relationships within this iconic group of fossil arthropods. Here we document an essentially complete ontogeny of the trilobite Redlichia cf. versabunda from the Cambrian Series 2 (late Stage 4) Ramsay Limestone of Yorke Peninsula in South Australia, including some of the best-preserved protaspides (the earliest biomineralized trilobite larval stage) known for any Cambrian trilobite. These protaspid stages exhibit similar morphological characteristics to many other taxa within the Suborder Redlichiina, especially to closely related species such as Metaredlichia cylindrica from the early Cambrian period of China. Morphological patterns observed across early developmental stages of different groups within the Order Redlichiida are discussed. Although redlichiine protaspides exhibit similar overall morphologies, certain ontogenetic characters within this suborder have potential phylogenetic signal, with different superfamilies characterized by unique trait combinations in these early growth stages.

The Ediacara Member of the Rawnsley Quartzite in the Flinders Ranges (South Australia) has undergone considerable investigation due to its placement within the package of terminal Ediacaran sediments in the region and as the host sediments of the Ediacara biota fossils. A focus on palaeoenvironment reconstruction and taphonomy has seen a succession of lithofacies models presented. These have evolved with the expansion of recognised Ediacara biota localities and prevailing palaeontological methodologies. Much of the recent descriptive lithofacies work has focused on the Nilpena fossil site in the west of the Flinders Ranges. This location is particularly fossil-rich but does not represent a "typical" section through the Ediacara Member. The Ediacara Member elsewhere in the region contains up to six parasequences with total thicknesses varying from ten to 260 m. With the exclusion of the Ikara-Chace Range region, the majority of studied locations external to Nilpena do not show clear evidence for significant (canyon-scale), intra-member erosional features. In this study we review existing facies models for the Ediacara Member and compile a "best-fit" revised facies model by incorporating the modern facies interpretations (largely based at Nilpena) and previous basin-wide observations, models and stratigraphic sections. The revised model is assessed against a series of newly measured stratigraphic sections from across the basin. We propose the division of the wave-base facies into two facies, representative of the upper and lower storm wave-base environments respectively and the re-inclusion of a facies representative of a shoreface palaeoenvironment. Additional characters and identifiers for the facies have been incorporated to aid field identification, as the ability to identify facies of fossil-bearing isolated hand-specimens can allow fossils found on scree slopes to be traced back to source beds. Likewise, palaeoenvironmental interpretations are critical to the reconstruction of Ediacara biota habitat and preservational environments. Refereed/Peer-reviewed

Despite 70 years of study, Dickinsonia remains one of the Ediacara biota’s most enigmatic taxa with both morphological characters and phylogenetic affinities still debated. A large population of relatively small Dickinsonia costata present on a semi-contiguous surface from the Crisp Gorge fossil locality in the Flinders Ranges (South Australia) provides an opportunity to investigate this taxon in its juvenile form. This population supports earlier findings that suggest D. costata’s early growth was isometric, based on the relationship between measured variables of length and width. The number of body units increases with length, but at a decreasing rate. A correlation between a previously described physical feature, present as a shrinkage rim partially surrounding some specimens and a novel, raised lip in some specimens, suggests that both features may have been the result of a physical contraction in response to the burial process, rather than due to a gradual loss of mass during early diagenesis. A marked protuberance in 15% of the population is also noted in limited specimens within the South Australian Museum collections and appears to be present only in juvenile D. costata. Both the abundance and narrow size range of this population support the notion that Dickinsonia was a hardy opportunist, capable of rapid establishment and growth on relatively immature textured organic-mat substrates.

The lower Cambrian (Cambrian Series 2, Stage 4) Emu Bay Shale Lagerstatte, which is by far the most important Burgess Shale-type (BST) deposit in Australia, occurs mainly in the bottom 10 m of the Emu Bay Shale at Big Gully on the north coast of Kangaroo Island, South Australia. In this area, the exposed Cambrian succession commences with the White Point Conglomerate, the bulk of which comprises a crudely cross-bedded cobble to boulder conglomerate with minor mudstone and sandstone facies. The conglomeratic horizons thin markedly to the south. The White Point Conglomerate was deposited as coalesced fan deltas derived from an uplifted tectonic margin immediately to the north of the present coastline. The White Point Conglomerate is overlain by the sandstone, siltstone and conglomerate beds of the Marsden Sandstone (new name), the basal 3 m of which is a distinctive fossiliferous argillaceous limestone and shale, the Rouge Mudstone Member (new name). Syndepositional folding and faulting affected both the White Point Conglomerate and Marsden Sandstone prior to the deposition of the Emu Bay Shale, the base of which represents a sequence boundary. The Lagerstatte occurs within dark grey to black laminated micaceous mudstone facies, some of which show evidence of syndepositional disturbance, and are interpreted to have been deposited in isolated stagnant, anoxic to oxic depressions on the sea floor, beneath a normally oxic water column, with a sharp redox boundary at the sediment-water interface; below this boundary the pore water was anoxic. Thin (up to 20 cm) structureless fine sandstone horizons within the mudstone are interpreted as either sediment gravity flow or storm deposits. The Lagerstatte-bearing mudstone beds thin southwards and disappear 500-600 m south of the coast. The Emu Bay Shale coarsens upwards; arthropod tracks are abundant in fine sandstone beds towards the top of the Emu Bay Shale. In coastal sections the sandstone facies of the Boxing Bay Formation rest conformably on the Emu Bay Shale; inland the contact is channelled. Refereed/Peer-reviewed

Two species of Anomalocaris co-occur in the Emu Bay Shale (Cambrian Series 2, Stage 4) at Big Gully, Kangaroo Island. Frontal appendages of Anomalocaris briggsi Nedin, 1995, are more common than those of Anomalocaris cf. canadensis Whiteaves, 1892, at a quarry inland of the wave-cut platform site from which these species were originally described. An oral cone has the three large, node-bearing plates recently documented for Anomalocaris canadensis, confirming that Anomalocaris lacks a tetraradial 'Peytoia' oral cone and strengthening the case for the identity of the Australian specimens as Anomalocaris. Disarticulated anomalocaridid body flaps are more numerous in the Emu Bay Shale than in other localities, and they preserve anatomical details not recognized elsewhere. Transverse lines on the anterior part of the flaps, interpreted as strengthening rays or veins in previous descriptions of anomalocaridids, are associated with internal structures consisting of a series of well-bounded, striated blocks or bars. Their structure is consistent with a structural function imparting strength to the body flaps. Setal structures consisting of a series of lanceolate blades are similar to those of other anomalocaridids and are found in isolation or associated with body flaps. A single specimen also preserves putative gut diverticula. The morphology of the appendages, oral cone, gut diverticula and compound eyes of Anomalocaris, along with its large size, suggests that it was an active predator, and specimens of coprolites containing trilobite fragments and trilobites with prominent injuries have been cited as evidence of anomalocaridid predation on trilobites. Based on frontal appendage morphology, Anomalocaris briggsi is inferred to have been a predator of soft-bodied animals exclusively and only Anomalocaris cf. canadensis may have been capable of durophagous predation on trilobites, although predation (including possible cannibalism) by Redlichia could also explain the coprolites and damage to trilobite exoskeletons found in the Emu Bay Shale. © The Palaeontological Association.

Despite the status of the eye as an “organ of extreme perfection”1, theory suggests that complex eyes can evolve very rapidly2. The fossil record has, until now, been inadequate in providing insight into the early evolution of eyes during the initial radiation of many animal groups known as the Cambrian explosion. This is surprising because Cambrian Burgess-Shale-type deposits are replete with exquisitely preserved animals, especially arthropods, that possess eyes3, 4, 5. However, with the exception of biomineralized trilobite eyes, virtually nothing is known about the details of their optical design. Here we report exceptionally preserved fossil eyes from the Early Cambrian (~515 million years ago) Emu Bay Shale of South Australia, revealing that some of the earliest arthropods possessed highly advanced compound eyes, each with over 3,000 large ommatidial lenses and a specialized ‘bright zone’. These are the oldest non-biomineralized eyes known in such detail, with preservation quality exceeding that found in the Burgess Shale and Chengjiang deposits. Non-biomineralized eyes of similar complexity are otherwise unknown until about 85 million years later6, 7. The arrangement and size of the lenses indicate that these eyes belonged to an active predator that was capable of seeing in low light. The eyes are more complex than those known from contemporaneous trilobites and are as advanced as those of many living forms. They provide further evidence that the Cambrian explosion involved rapid innovation in fine-scale anatomy as well as gross morphology, and are consistent with the concept that the development of advanced vision helped to drive this great evolutionary event8, The Australian Research Council (grant LP0774959), South Australian Museum, Spanish Ministry of Science (RYC2007-00090 and grant CGL2009-07073), Beach Energy and Sealink Pty Ltd for funding

Until recently1, intricate details of the optical design of non-biomineralized arthropod eyes remained elusive in Cambrian Burgess-Shale-type deposits, despite exceptional preservation of soft-part anatomy in such Konservat-Lagerstätten2, 3. The structure and development of ommatidia in arthropod compound eyes support a single origin some time before the latest common ancestor of crown-group arthropods4, but the appearance of compound eyes in the arthropod stem group has been poorly constrained in the absence of adequate fossils. Here we report 2–3-cm paired eyes from the early Cambrian (approximately 515 million years old) Emu Bay Shale of South Australia, assigned to the Cambrian apex predator Anomalocaris. Their preserved visual surfaces are composed of at least 16,000 hexagonally packed ommatidial lenses (in a single eye), rivalling the most acute compound eyes in modern arthropods. The specimens show two distinct taphonomic modes, preserved as iron oxide (after pyrite) and calcium phosphate, demonstrating that disparate styles of early diagenetic mineralization can replicate the same type of extracellular tissue (that is, cuticle) within a single Burgess-Shale-type deposit. These fossils also provide compelling evidence for the arthropod affinities of anomalocaridids, push the origin of compound eyes deeper down the arthropod stem lineage, and indicate that the compound eye evolved before such features as a hardened exoskeleton. The inferred acuity of the anomalocaridid eye is consistent with other evidence that these animals were highly mobile visual predators in the water column5, 6. The existence of large, macrophagous nektonic predators possessing sharp vision—such as Anomalocaris—within the early Cambrian ecosystem probably helped to accelerate the escalatory ‘arms race’ that began over half a billion years ago7, 8., The Australian Research Council (grant LP0774959), South Australian Museum, University of Adelaide, MICINN-Spanish Ministry of Science (RYC2007-00090 and grant CGL2009-07073), Beach Energy and Sealink Pty Ltd for funding.

The lower Cambrian Emu Bay Shale on Kanga- roo Island, South Australia, contains the only known Cambrian Burgess Shale-type biota in Australia. Two new lamellipedian arthropods, Emucaris fava gen. et sp. nov. and Kangacaris zhangi gen. et sp. nov., from the Emu Bay Shale Lagerstatte are described as monotypic genera that are resolved cladistically as a monophyletic group that is sister to Naraoiidae + Liwiidae and classified within the Nekta- spida as a new family Emucarididae. Shared derived characters of Emucarididae involve a bipartite, elongate hypostome and elongation of the pygidium relative to the cephalic shield and very short thorax. A monophyletic Liwiidae is composed of Liwia and the Ordovician Taric- coia + Soomaspis but excludes Buenaspis, and even the membership of Buenaspis in Nektaspida is contradicted amongst the shortest cladograms. New morphological inter- pretations favour affinities of Kwanyinaspis with Conciliter- ga rather than with Aglaspidida, and Phytophilaspis with Petalopleura.

Abundant material from a new quarry excavated in the lower Cambrian Emu Bay Shale (Kangaroo Island, South Australia) and, particularly, the preservation of soft-bodied features previously unknown from this Burgess Shale-type locality, permit the revision of two bivalved arthropod taxa described in the late 1970s, Isoxys communis and Tuzoia australis. The collections have also produced fossils belonging to two new species: Isoxys glaessneri and Tuzoia sp. Among the soft parts preserved in these taxa are stalked eyes, digestive structures and cephalic and trunk appendages, rivalling in quality and quantity those described from better-known Lagerstätten, notably the lower Cambrian Chengjiang fauna of China and the middle Cambrian Burgess Shale of Canada.

Refereed/Peer-reviewed