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.

Exquisitely preserved three-dimensional examples of the classic Ediacaran (late Neoproterozoic; 570–541 Ma) frond Charniodiscus arboreus Jenkins and Gehling, 1978 (herein referred to as Arborea arborea Glaessner in Glaessner and Daily, 1959) are reported from the Ediacara Member, Rawnsley Quartzite of South Australia, and allow for a detailed reinterpretation of its functional morphology and taxonomy. New specimens cast in three dimensions within sandy event beds showcase detailed branching morphology that highlights possible internal features that are strikingly different from rangeomorph and erniettomorph fronds. Combined with dozens of well-preserved two-dimensional impressions from the Flinders Ranges of South Australia, morphological variations within the traditional Arborea morphotype are interpreted as representing various stages of external molding. In rare cases, taphomorphs (morphological variants attributable to preservation) represent composite molding of internal features consisting of structural supports or anchoring sites for branching structures. Each primary branch consists of a central primary branching stalk from which emerge several oval secondary branches, which likely correspond to similar structures found in rare two-dimensional specimens. Considering this new evidence, previous synonymies within the Arboreomorpha are no longer justified, and we suggest that the taxonomy of the group be revised.

The Devonian of the Carnic Alps (Austria) is developed in different facies. The shallow marine facies is up to 1200m thick. The Feldkogel Limestone of the Polinik Formation, >330m thick, was dated as Eifelian—Late Devonian. The Feldkogel Limestone at Mount Polinik is developed in a peritidal facies composed of subtidal, intertidal, and supratidal deposits. Subtidal sediments are represented by dark gray Amphipora limestone and intertidal deposits by laminated and partly bioturbated grainstone and packstone, ostracode wackestone to packstone, and locally intercalated intraclast breccias documenting tidal channel fills. Laminated microbial mats (stromatolites) formed in a supratidal depositional environment. Grainstone and packstone contain abundant unilocular parathuramminid foraminifers. This latter group encompasses a diversified assemblage of ivanovellids, parathuramminids, uralinellids, and irregularinoids; some earlandiids are also present. They are dated herein as late Eifelian—early Givetian. These foraminifers provide a more precise systematics of these taxa, which often have not been studied for more than half a century. The taxonomic problems of their assignment to foraminifers, pseudo-foraminifers, calcitarcha, thaumatoporellaceans, volvocaleans, or other algae are also discussed. Several taxa are emendated: Parathuramminida, Parathuramminoidea, Irregularinoidea, Eovolutinidae, Ivanovellidae, Parathuramminidae, Uralinellidae, Ivanovella, Elenella, Neoarchaesphaera, Parathurammina, Bykovaella, Uralinella, and Paracaligella. The new taxa are: Ivanovella reitlingerae n. sp., Elenella polinikensis n. sp., Uralinella sabirovi n. sp., and Radiosphaerella poyarkovi n. sp.

Turritellid gastropods are important components of many Cretaceous—Recent fossil marine faunas worldwide. Their shell is morphologically simple, making homoplasy widespread and phylogenetic analysis difficult, but fossil and living species can be recognized based on shell characters. For many decades, it has been the consensus that the oldest definite representatives of Turritellidae are from the Lower Cretaceous, and that pre-Cretaceous forms are homeomorphs. Some morphological characters of the present turritelline species resemble those of mathildoids, but many diagnostic characters clearly separate these two groups. We here describe and/or redescribe—based on examination of more than 2600 near complete specimens—four species from the Upper Jurassic Dhosa Oolite Member of the Chari Formation in Kutch, western India, and demonstrate that they are members of Turritellidae, subfamily Turritellinae, on the basis of diagnostic characters including apical sculptural ontogeny (obtained from SEM study), spiral sculpture, and growth line patterns. The four species are in order of abundance, Turritella jadavpuriensis Mitra and Ghosh, 1979; Turritella amitava new species; Turritella jhuraensis Mitra and Ghosh, 1979, and Turritella dhosaensis new species. The turritelline assemblages occur only on the northeastern flank of the Jhura dome (23°24′47.57″N, 69°36′09.26″E). Age of the Dhosa Oolite has recently been confirmed based on multiple ammonite species. All these points indicate that these fossils are the oldest record of the family Turritellidae—by almost 30 million years—in the world.

We examine the morphological variation of a Paleozoic pterineid during a time of relative ecological and taxonomic stability in the Middle Devonian Appalachian Basin in central and eastern New York. We discuss the taxonomic status of the Middle Devonian bivalve Actinopteria boydi (Conrad, 1842) and quantify the variability of its shell disk as well as the width and angle of the auricles and sulci of this otherwise character-poor bivalve species using geometric morphometric techniques employing Cartesian landmarks. We compare variants from three stratigraphic levels (Skaneateles, Ludlowville, and Moscow formations) and from different habitats characterized by lithofacies.

The phenotypic variation observed in our data does not amount to an overall directional shift in morphology, i.e., they constitute reversible changes of morphology in a single variable taxon. Our study finds small-scale variation in morphology that represents evidence for ecophenotypic variation through ~3–4 Myr. Differences in substrate coupled with water energy seem to impact this taxon's morphology. Although no clearly separated groups can be observed, material from muddy facies develops variants with, on average, rounder and broader shell disks than are found in material from silty facies. This morphology could have increased the flow rate of water channeled over the posterior shell portion thereby improving filtration rate, which is especially beneficial in environments with low water energy.

Actinocerid nautiloids from the Lhasai Formation in the Xainza region are studied systematically for the first time. The nautiloids are identified as Middle Ordovician in age based on stratigraphic correlations with those from North China, Sibumasu, North Australia (northern Gondwana), and North America (Laurentia). A cluster analysis shows strong affinities between the actinocerid nautiloids of the Lhasa Terrane and those of the Himalaya, North China, and Sibumasu terranes. Our results support Middle Ordovician paleogeographic reconstructions that place North China rather than South China much closer to Australia. Nine species assigned to six genera of Meitanoceratidae, Wutinoceratidae, Armenoceratidae, Ormoceratidae, and Discoactinoceratidae are described in detail: Pomphoceras nyalamense (Chen, 1975), Pomphoceras yaliense (Chen, 1975), Wutinoceras cf. W. foerstei (Endo, 1930), Mesowutinoceras giganteum Chen in Chen and Zou, 1984, Armenoceras tani (Grabau, 1922), Armenoceras teicherti Endo, 1932, Armenoceras xizangense new species, Deiroceras globosom Zou and Shen in Chen and Zou, 1984, and Discoactinoceras cf. D. multiplexum Kobayashi, 1927.

Tarphycerids were diverse and abundant in Ordovician marine faunas. Beginning at the Late Ordovician extinction, the diversity of tarphycerids declined throughout the Silurian, until their extinction in the latest Silurian. Two genera survived the Late Ordovician extinction: Trocholites Conrad, 1838 (from which Ophioceras Barrande, 1865 probably diverged) and Discoceras Barrande, 1867 (= Graftonoceras Foerste, 1925). Discoceras graftonense (Meek and Worthen, 1870), so far known from the US, China, and Australia, is recorded from the Silurian of Bohemia and Gotland. Discoceras stridsbergi n. sp., D. lindstroemi n. sp., and D. sp. indet. from the Wenlock of Gotland and D. amissus (Barrande, 1865) from the Llandovery of Bohemia are all endemic species probably derived from D. graftonense. The distribution of D. graftonense and the origin of four species of Discoceras in the latest Sheinwoodian and early Homerian represent the last diversification and dispersion of the Tarphycerida. No tarphycerid species originated after the mid-Homerian extinction (Mulde and Lundgreni events). Silurian Discoceras retained the morphology and habitats of their Ordovician ancestors. The hatching time and autecology of juveniles has remained unclear. Evidence from the material studied suggests that juveniles were planktonic in habit, possessing a minute curved shell with few phragmocone chambers. Discoceras lindstroemi n. sp. is exceptional owing to its heteromorphic planispiral shell with coiling that changed during ontogeny, resulting in a changing aperture orientation and decreased maneuverability.

The bryozoan genus Aspidostoma Hincks, 1881 has been regarded as the only representative of the Aspidostomatidae Jullien, 1888 in Argentina to date. Its type species, Aspidostoma giganteum (Busk, 1854), is presently distributed in the Magellanic Region (Argentina and Chile) and has been recorded in Oligocene and Miocene fossil deposits of Santa Cruz and Chubut, respectively. New material from San Julián (late Oligocene), Monte León (early Miocene), Chenque (early to middle Miocene), and Puerto Madryn (late Miocene) formations suggests, however, that A. giganteum is not represented in the fossil record. Material from Puerto Madryn Formation previously regarded as A. giganteum is here recognized as Aspidostoma roveretoi new species. Aspidostoma ortmanni Canu, 1904 is revalidated for the species from the San Julián Formation. Aspidostoma armatum new species and Aspidostoma tehuelche new species are introduced for material from the Monte León and Chenque formations, respectively. Aspidostoma incrustans Canu, 1908, from the early Miocene, is redescribed. Melychocella Gordon and Taylor, 1999, which differs from Aspidostoma in having vicarious avicularia and lacking a median ridge and a quadrangular process proximal to the opesia-orifice, is so far represented by three Paleogene species from the Chatham Islands (Southwest Pacific). The material from Monte León allowed us to transfer Aspidostoma flammulum Canu, 1908 to Melychocella, resulting in the new combination Melychocella flammula (Canu, 1908). Melychocella biperforata new species is described from the lower Miocene Monte León and Chenque formations. The presence of Melychocella in the Neogene of Patagonia extends its geographic distribution and its temporal range.

The Ediacaran to lower Cambrian Chilhowee Group of the southern and central Appalachians records the rift-to-drift transition of the newly formed Iapetan margin of Laurentia. Body fossils are rare within the Chilhowee Group, and correlations are based almost exclusively on lithological similarities. A critical review of previous work highlights the relatively weak biostratigraphic and radiometric age constraints on the various units within the succession. Herein, we document a newly discovered fossil-bearing locality within the Murray Shale (upper Chilhowee Group) on Chilhowee Mountain, eastern Tennessee, and formally describe a nevadioid trilobite, Buenellus chilhoweensis n. sp., from that site. This trilobite indicates that the Murray Shale is of Montezuman age (provisional Cambrian Stage 3), which is older than the Dyeran (provisional late Stage 3 to early Stage 4) age suggested by the historical (mis)identification of “Olenellus sp.” from within the unit as reported by workers more than a century ago. Buenellus chilhoweensis n. sp. represents only the second known species of Buenellus, and demonstrates that the genus occupied both the Innuitian and Iapetan margins of Laurentia during the Montezuman. It is the oldest known trilobite from the Iapetan margin, and proves that the hitherto apparent absence of trilobites from that margin during the Montezuman was an artifact of inadequate sampling rather than a paleobiogeographic curiosity. The species offers a valuable biostratigraphic calibration point within a rock succession that has otherwise proven recalcitrant to refined dating.

A new genus and species of the planktonic shrimp family Luciferidae, Sume marcosi n. gen. n. sp., is described and illustrated from material collected in calcareous shale of the late Early Cretaceous (Aptian-Albian) Romualdo Formation, Araripe Basin, northeastern Brazil. The material is very well preserved, including the antennae, stalked eyes, second and third maxillipeds, pleopods, and uropods, and represents the first described fossil of the family Luciferidae.

Kerguelen Islands are predominantly volcanic lands, thus fossil references are very uncommon. However, its Miocene fossils are of specific interest for understanding migration routes of some taxa during the Cenozoic, given the intermediary position of Kerguelen with various continents. Despite this fossil rarity, we studied herein hundreds of nodules corresponding to the sole known fossil brachyurans (and unique Decapoda) from Kerguelen both for their systematics and their preservation. Indeed, these crabs display some internal fragile structures that are rarely fossilized, such as the gills' branchial lamellae, preserved in volume. The preservation of these gills and their diagenetic features were documented through traditional imagery (SEM), including morphological comparison to modern gills, and with petrographic and geochemical analyses (EDS, X-ray diffractometry). Some cheilostome bryozoans were observed as probable foulers of the crabs carcasses. The fossil material corresponds to a new cancrid crab (Romaleon franciscae n. sp.) and its occurrence may imply a novel route from South America westward for the geographic migration of the genus Romaleon, since its Cretaceous emergence. The cup-shape and the number and the organization of the gills in these fossil Cancridae specimens are similar to those observed in their extant representatives. Gill preservation in 3D is linked to very early phosphatization of the system during diagenesis, as shown by the nodule matrix, and likely to deposition of a thin clayey cover on the soft-tissues. The implication of intrinsic phosphorous in the differential phosphatization of the crabs' anatomy remains difficult to determine.

A new helminthomorph millipede, Sinosoma luopingense new genus new species, from the Triassic Luoping biota of China, has 39 body segments, metazonites with lateral swellings that bear a pair of posterolateral pits (?insertion pits for spine bases), and sternites that are unfused to the pleurotergites. This millipede shares a number of characters with nematophoran diplopods, but lacks the prominent dorsal suture characteristic of that order. Other “millipede” material from the biota is more problematic. Millipedes are a rare part of the Luoping biota, which is composed mainly of marine and near-shore organisms. Occurrences of fossil millipedes are exceedingly rare in Triassic rocks worldwide, comprising specimens from Europe, Asia, and Africa, and consisting of juliform millipedes and millipedes that are either nematophorans or forms very similar to nematophorans.

The Upper Ordovician (lower Katian) Bobcaygeon and Verulam formations from the Lake Simcoe region of Ontario contain a highly diverse echinoderm assemblage that is herein recognized as a Konservat-Lagerstätte. Although fossil crinoids have long been recognized from these formations, the fauna has not received a comprehensive taxonomic evaluation since Springer's classic 1911 monograph. Recent extensive collection and preparation of new material from the Bobcaygeon and Verulam formations near Brechin, Ontario recovered numerous exceptionally preserved crinoid specimens with arms, stems, and attachment structures intact. The Brechin Lagerstätte is the most taxonomically diverse Katian crinoid fauna, with more than 20 crinoid genera represented in this collection.

Here, all dicyclic crinoids belonging to subclass Camerata from the Brechin Lagerstätte are evaluated. The following four genera and seven species are described from the fauna, including one new genus and four new species: Reteocrinus stellaris, Reteocrinus alveolatus, Archaeocrinus sundayae n. sp., Archaeocrinus maraensis n. sp., Priscillacrinus elegans n. gen. n. sp., Cleiocrinus regius, and Cleiocrinus lepidotus n. sp. The exceptional preservation of this collection provides an opportunity to describe more fully the morphologic and ontogenetic details of known Ordovician crinoid taxa, to conduct a taxonomic re-evaluation of many species, to describe new taxa, and to provide a framework for subsequent studies of crinoid community paleoecology.

The extreme rareness of Sardinian fossil sites older than Middle and Late Pleistocene makes the Monte Tuttavista karst complex (E Sardinia, Italy) very important. Remarkable lagomorph material, recovered from several fissure infillings of Monte Tuttavista referable to the Capo Figari/Orosei 1 and Orosei 2 faunal sub-complexes (early Pleistocene, ∼2.1/1.9–1.1 Ma), allowed us to describe a new endemic insular leporid, Sardolagus obscurus n. gen. n. sp. The new taxon is characterized by a peculiar combination of an advanced p3 (Lepus-type) and a primitive P2 lacking deep flexa. The origin of such discrepancy, unprecedented among continental and insular endemic European leporids, is unclear. It could be the result of: (1) an independent evolution of p3 from an ancestor bearing the primitive P2/p3 (e.g., Alilepus, Hypolagus), or (2) a selective reversal morphocline from an Oryctolagus/Lepus-like leporine. The lack of data about the phylogenetic origin of the new taxon makes any inference about its possible arrival to Sardinia problematic. Crossing the European leporid records and evidence of migrations to Sardinia, we hypothesize three possible ages in which the ancestor of Sardolagus obscurus could have arrived in Sardinia, restricted to the late Miocene-early/late Pliocene (∼8–3.6 Ma). The phylogenetic relationship between Sardolagus obscurus n. gen. n. sp. and the oldest Sardinian leporid, recorded from Capo Mannu D1 and dated at the early/late Pliocene boundary (∼3.6 Ma), is unclear at present, however it is quite likely that they pertain to the same lineage.