The enigmatic fossil Moniopterus japonicus Hatai et al., 1974 from the early Middle Miocene Moniwa Formation of northern Japan has been described as the only known example of fossil sea-snake eggs and also as fossilized pupal chambers of a coleopteran insect. A reexamination of the holotype provides no evidence in support of these previous interpretations. Scanning electronic microscopy and computed tomography observations on the holotype reveal that the calcareous lining, previously interpreted as eggshell, is instead composed of irregular spherulitic prisms, thin in the middle and becoming thicker toward both ends. In addition to the elongate oval shape and the presence of an opening at the more pointed end, these observations strongly suggest that M. japonicus is a boring of the mytilid boring bivalve Lithophaga isolated from the host rock. This reinterpretation is further supported by the occurrence of similar isolated and in situ borings with Lithophaga shells within the type and a nearby locality. Regarding this fossil as an ichnofossil makes the generic name Moniopterus a junior synonym of Gastrochaenolites Leymerie, 1842 and the species name japonicus is a senior synonym of Gastrochaenolites torpedo Kelly and Bromley, 1984. G. torpedo should thus be replaced with Gastrochaenolites japonicus (Hatai et al., 1974).

A diverse assemblage of Middle Cambrian sponges, recently collected from the Wheeler and Marjum Formations of western Millard County, Utah, includes a variety of demosponges and hexactinellids. This collection includes the verongiid Vauxia bellula Walcott, 1920, and the protomonaxonids Choia carteri and Choia ridleyi Walcott, 1920, Hamptonia bowerbanki Walcott, 1920, and Hamptonia parva n. sp. Hexactinellids in the collection include the reticulosid protospongioids Diagoniella hindei Walcott, 1920, and Diagoniella magna n. sp.; the dierespongioid hydnodictyid Valospongia? gigantus Rigby, 1973; and the hintzespongioid Hintzespongia bilamina Rigby and Gutschick, 1976. A specimen of the problematic Sentinelia? draco Walcott, 1920, is also documented as part of the collection.

New specimens of an as yet unidentified carnivoran from the earliest Paleocene of Saskatchewan are described. The new specimens augment the evidence on which the contentious earliest (middle Puercan) occurrence of Carnivora is based, provide novel information of the lower dentition of the earliest carnivorans, and provides evidence for the earliest taxonomic diversity in Carnivora.

The seven species of extant sea turtles show a diversity of diets and feeding specializations. Some of these species represent distinctive ecomorphs that can be recognized by osteological characters and therefore can be identified in fossil taxa. Specifically, modifications to the feeding apparatus for shearing or crushing (durophagy) are easily recognizable in the cranium and jaw. New sea turtle fossils from the Miocene of Peru, described as a new genus and species (Pacifichelys urbinai n. gen. and n. sp.), correspond to the durophagous ecomorph. This new taxon is closely related to a recently described sea turtle from the middle Miocene of California, USA (Pacifichelys hutchisoni n. comb.), providing additional information on the osteological characters of this lineage. A phylogenetic analysis of Pacifichelys and other pan-chelonioid sea turtle lineages shows that at least seven lineages independently evolved feeding specialized for shearing or crushing. the iterative evolution of these morphologies is plausibly linked to ecological factors such as the development of seagrass communities and the opening of niches through extinction that occurred from the Cretaceous to the Miocene.

A new genus and species of edrioasteroid grade echinoderm, Kailidiscus chinensis, is described from the Kaili Biota of the basal lower Middle Cambrian Kaili Formation from Guizhou Province, China. This echinoderm has a strong resemblance to isorophid edrioasteroids, bearing a well-developed peripheral rim, long curved ambulacra, and slightly imbricate interambulacral plating at maturity. However, the presence of pore-bearing, double biserial floor plates, tiered cover plates, lack of radially positioned oral frame plates, and unincorporated hydropore/gonopore are unknown in isorophids. Many of these features bear strong resemblance to eocrinoids and helicoplacoids, attesting to the plesiomorphic nature of this taxon. Despite the obvious anatomical differences, specimens of this species preserve a complete ontogeny that resembles that of isorophids. Juveniles show a discoidal theca with straight ambulacra that transitions to an inflated theca with strongly curved ambulacra with maturity.

Fossils of the giant short-faced bear, Arctodus simus (Cope, 1879), have been recovered from over 100 localities in North America, extending from Mexico to Alaska and California to Virginia. Despite this large range, the species has never been recorded from the southeastern United States. The lesser short-faced bear, Arctodus pristinus Leidy, 1854 is well represented from this region, particularly Florida, but all known occurrences are late Pliocene – middle Pleistocene in age (about 2.5 to 0.3 Ma). Differentiating A. simus from A. pristinus can be difficult because large individuals of A. pristinus overlap in size with small individuals of A. simus, and there are few morphological differences. However, these two taxa can be clearly separated based on the relative proportions of their molars and premolars. Two Pleistocene records of A. simus representing a minimum of three individuals from the Withlacoochee River drainage of central Florida are reported here, substantially extending the distribution of this massive bear into southeastern North America. A late Pleistocene age for these occurrences is corroborated by an associated Rancholabrean fauna and rare earth elemental analyses. One of the reported individuals is quite large, supporting the hypothesis of extreme sexual dimorphism in A. simus and rejecting a hypothesis of two subspecies.

Four species of rugose corals (one new) are described from the Silurian of the Kurosegawa Terrane, Southwest Japan. They are Neobrachyelasma japonica n. sp., Pseudamplexus sp., Amsdenoides sp., and Amplexoides sp. aff. A. chaoi (Grabau, 1925). These species occur in the Middle Member of the Gionyama Formation, which is Late Llandovery to Early Ludlow in age. Neobrachyelasma is reported for the first time from Japan. This genus occurs in the Lower Llandovery to Upper Silurian of Japan, South China, Kazakhstan, and the Altai and might be distributed only in South China and Japan during the Late Llandovery. Its occurrence in Japan may support a paleogeographic proximity of ‘Proto-Japan’ and the South China Block during the Silurian.

Cambrothyra ampulliformis Qian and Zhang, 1983, is a jar- or vase-shaped fossil known from the Lower Cambrian of Shaanxi and Hubei provinces, China. It has been interpreted as a protistan test or cyst or a metazoan sclerite. A large collection of specimens from the Xihaoping Member of the Dengying Formation in southern Shaanxi Province permits its detailed redescription. These fossils are highly variable in shape but this variation is continuous and does not support the current recognition of multiple species for this material. They were originally hollow with a restricted basal foramen and a calcareous wall probably composed of fibrous aragonite. All of these features support the identification of Cambrothyra as sclerites of a coeloscleritophoran, a problematic group of Cambrian scleritome-bearing metazoans. Furthermore, the walls of Cambrothyra sclerites contain numerous pores, a feature shared with other coeloscleritophorans. Cambrothyra resembles chancelloriids in particular due to the shared presence of a verruculose texture around the foramen and the absence of mirror-image pairs of asymmetric sclerites. However, unlike chancelloriids, which have rosette-like compound sclerites, the scleritome of Cambrothyra was dominated by isolated sclerites, with only a few pairs and clusters of sclerites and twin sclerites. Consequently, we hypothesize that Cambrothyra forms a clade with other chancelloriids, but represents a basal lineage that plesiomorphically retained isolated sclerites. The morphology of Cambrothyra sclerites, which shares features with both chancelloriids and halkieriids, thus supports the hypothesis that all coeloscleritophorans form a natural group.

The Lower Ferron Sandstone Member of the Mancos Shale in southeastern Utah preserves a chondrichthyan assemblage of at least 13 taxa that include: Hybodus sp., Ptychodus cf. P. mammillaris Agassiz, 1843, Ptychodus whipplei Marcou, 1858, cf. Chiloscyllium sp., Scapanorhynchus raphiodon (Agassiz, 1843), Cretodus crassidens (Dixon, 1850), cf. Leptostyrax sp., cf. Cretalamna appendiculata (Agassiz, 1835), Squalicorax sp., Pseudohypolophus mcnultyi (Thurmond, 1971), Protoplatyrhina hopii Williamson, Kirkland and Lucas, 1993, Ischyrhiza schneideri (Slaughter and Steiner, 1968), and Ptychotrygon triangularis (Reuss, 1844). Although this assemblage is typical of other Turonian chondrichthyan faunas in North America, fossil teeth are preserved in two unique facies associations that consist of arenitic sandstones with mud interclasts and rounded chert, feldspar, and quartz pebbles. the coarser beds within these facies associations are previously interpreted to represent storm events and turbidity flows associated with a sea level lowstand. Chondrichthyan teeth occurring within these coarser beds are indicative of extensive transport and reworking and attest to the durable nature of chondrichthyan teeth for biostratigraphic and paleoecological interpretations. Similar studies of chondrichthyan teeth in shelf marine settings may also provide new insights for facies interpretations related to sequence stratigraphy and regional stratigraphic correlations.

The order Litopterna is represented in the São José de Itaboraí basin by four species belonging to the families Protolipternidae (Protolipterna ellipsodontoides, Miguelsoria parayirunhor and Asmithwoodwardia scotti) and Proterotheriidae (Paranisolambda prodromus). Only the deciduous teeth of P. prodromus are known so far. Isolated milk premolars are described for P. ellipsodontoides and M. parayirunhor. The known specimens assigned to P. prodromus are redescribed. No milk teeth are known for A. scotti. The upper and lower milk teeth of Protolipternidae, especially dP3, are more molarized than their successors, resembling, in several features later Proterotheriidae. They provide new support for the placement of this family within the order Litopterna. The analysis of the wear level of dp2-4/dP2-4 and X-ray images of the lower jaw of P. prodromus suggests that the second teeth of the premolar series, in upper and lower jaw, are retained milk premolars. Some information on tooth replacement pattern of P. ellipsodontoides and P. prodromus are also provided.

Ptiloncodus Harris, 1962, a hook-shaped microfossil, is present in late Floian through Hirnantian [=late Ibexian through Gamachian] rocks in regions marginal to Laurentia. Specimens from the Great Basin provide additional information about this enigmatic microfossil. Two fused clusters of Ptiloncodus elements from western Utah do not duplicate clusters reported previously from coeval strata in central Nevada. EDS spectra confirm the long-standing assumption that these fossils are composed of calcium phosphate. SEM images show that short crystallites are aligned to provide fibrous surficial ultrastructure in the hooked part of these fossils, but more open arrangement is displayed at the top of the shank where paired lobate structures are attached. The join between the lobes and the shank is weak; these two parts of the fossil separate easily so that most specimens did not retain lobes. The shanks end in rounded terminations or in paired knobs that range from low protuberances to near hornlike features. The new data do not support any of several suggestions that compare Ptiloncodus to extant organisms, and uncertainty continues about its affinity and the function of its skeletal elements.

Morphometric analyses of shell morphology in the Pennsylvanian nautiloid Metacoceras mcchesneyi Murphy, 1970 (Cephalopoda, Mollusca) recovered from coal mines in Madison Township, Columbiana County, Ohio, USA, reveal the ontogenetic change from hatching to maturity as well as intra-specific variation of shell morphology. The shell shape of M. mcchesneyi has isometric relationships, and the umbilicus diameter between umbilical shoulders has a positive allometric relationship with shell diameter. These show that the relative whorl shape was constant through the ontogeny, but the umbilicus became relatively broader with growth. The siphuncle position moved from a ventro-central position toward the center with growth until 420° of the total rotational angle had been attained. A constriction was recognized on the early whorl at 9.5 mm in shell diameter, and the interval angles of succeeding septa were changed at the 5th septum, indicating that hatching occurred at this diameter. The ventral apertural wall, the disappearance of ornamentation toward the last preserved aperture, and the last whorl separating from the previous whorl indicate that M. mcchesneyi attained maturity at ca. 70 mm in shell diameter. Most characteristics of shell morphology in M. mcchesneyi (the relative shell shape and ornamentation through ontogeny) are comparable to those in modern and younger fossil nautilids, irrespective of taxonomy and age, supporting the conclusion that evolutionary rates of shell morphology are conservative in nautilid history.

A primitive paromomyid plesiadapiform primate, Edworthia lerbekmoi new genus and species, is described from a recently discovered locality in the Paskapoo Formation, exposed at a road cut in Edworthy Municipal Park, Bow River Valley, Calgary, Alberta, Canada. The new taxon, probably middle Torrejonian (To2) in age, is based on two dentary fragments containing well-preserved dentitions that bracket p2-4, m1-3. With the exception of the basal Paromomys, E. lerbekmoi differs from all other paromomyids in retaining p2, but p2 in the new paromomyid is single-rooted, not two-rooted as in Paromomys. E. lerbekmoi differs further from Paromomys in having an enlarged anterior alveolus for a tooth immediately anterior to p2, hypothesized to be il. Unlike other paromomyids with an enlarged il, however, this tooth in E. lerbekmoi was obliquely, not horizontally, oriented and its alveolus opens dorsally, in the alveolar row, not anteriorly, as in other paromomyids in which il is greatly enlarged. This suggests that E. lerbekmoi represents a previously unknown paromomyid lineage that evolved from an ancestor having obliquely oriented lower incisors as in the basal primate Purgatorius, not from an ancestor in which il was already subhorizontal in orientation, as in Paromomys. If this working hypothesis is correct or whether in the future some other evolutionary scenario will better account for the unique anterior dentition in E. lerbekmoi, the new paromomyid nonetheless demonstrates that crucial aspects of the earliest history of the important plesiadapiform family Paromomyidae remain to be discovered.

The ontogeny of Belosaepia ungula Gabb, 1860 from the Crockett Formation (Bartonian stage, Eocene) of Texas is documented for growth from embryo to old age. During the last stage of life, much skeletal resorption occurred, resulting in a major change in form of the skeleton. the animal produced a large skeleton (to 180 mm in length and 50 mm in diameter) with endogastric coiling, oblique septa and a very large siphuncle. the skeleton has a guard with a solid posterior prong, a posteroventral corona plate and a noded dorsal shield. the ventral margin of the skeleton consists of a thin flattened deck containing strongly recurved septa, conotheca and a secondary prismatic shell layer. New terms are defined for features of the skeleton not previously described. the microstructure of the ventral deck and the presence of a rod structure between the prong and callus are described for the first time. Chamberlets similar to those in living Sepia cuttlebones are present between closely spaced septa and they vary from walled units on lateral margins to pillar form in mid-ventor. the siphuncle is secondarily thickened within the dorsal interior, producing a siphuncle band. the skeleton was produced by a deep-bodied animal of demersal life habits. the species B. uncinata, B. harrisi and B. alabamensis voltzi proposed by Palmer (1937) are synonymised with B. ungula. the species B. veatchii and B. saccaria of Palmer (1937) are considered to be valid species, but B. alabamensis proposed by Palmer (1937) is synonymised with B. veatchii. Descriptions of belosaepiid species must be based only on specimens of adult size that have not been affected by resorption.

A new genus of long-horned chasmosaurine ceratopsid is described from the Dinosaur Park Formation (upper Campanian) of Western Canada. Mojoceratops perifania is represented by a skull and a parietal from the Dinosaur Park Formation of Alberta and an isolated parietal from the Dinosaur Park Formation of Saskatchewan. Several other specimens are provisionally referred to this taxon. While Mojoceratops shares many plesiomorphies with Chasmosaurus, the animal lacks the forward-curving parietal epoccipitals and reduced postorbital horns that diagnose the genus Chasmosaurus, and it differs from all other chasmosaurines in exhibiting a prominent sulcus on the anterior margin of the parietal, swellings on the anterodorsal surface of the parietal rami, and a small accessory process on the first parietal epoccipital. Other unusual features include anteriorly extended parietal fenestrae, a broad, heart-shaped frill, and transverse expansion of the postfrontal fontanelle. The type material of “Eoceratops canadensis” and “Chasmosaurus kaiseni” are nondiagnostic and these names are therefore considered nomina dubia, but their morphology is consistent with Mojoceratops and they probably belong to this genus. The frill of Mojoceratops shows marked variation. Some of this variation probably results from intraspecific variation or ontogenetic changes, but because the Dinosaur Park Formation encompasses more than a million years of time, evolution may explain some of these differences. Phylogenetic analysis shows that Mojoceratops forms a clade with Agujaceratops mariscalensis; Chasmosaurus is the most basal member of Chasmosaurinae.

This study presents the first record of Eocene birds from the western margin of southernmost South America. Three localities in Magallanes, southern Chile, have yielded a total of eleven bird remains, including Sphenisciformes (penguins) and one record tentatively assigned to cf. Ardeidae (egrets). Two different groups of penguins have been recognized from these localities. The first group is similar in size to the smallest taxa previously described from Seymour Island, Marambiornis Myrcha et al., 2002, Mesetaornis Myrcha et al., 2002, and Delphinornis Wiman, 1905. The second recognized group is similar in size to the biggest taxa from Seymour Island; based on the available remains, we recognize the genus Palaeeudyptes Huxley, 1859, one of the most widespread penguin genera in the Southern Hemisphere during the Eocene. The stratigraphic context of the localities indicates a certain level of correlation with the geological units described on Seymour Island. The newly studied materials cast more light on the paleobiogeography of the group, extending the known ranges to the South American continent. In addition to the newly discovered birds, the presence of several taxa of elasmobranchs previously recovered exclusively from Eocene beds in the Southern Hemisphere help to clarify the age of the studied localities, widely discussed during the last decades. This paper verifies the presence of extensive Eocene sedimentary successions with fossil vertebrates along the western margin of southern South America, contrary to the previous assumption that such a record is lacking in Chile.

A well-preserved highly diverse radiolarian fauna was discovered from the Upper Permian Dalong Formation in Guangxi, South China. A new genus and 19 species are described in this paper. Zhuangodiscus n. gen. belongs to the Family Relindellidae Kozur and Möstler. The 19 species include eight new species (Albaillella bialata, Neoalbaillella camarata, Neoalbaillella cephalota, Zhuangodiscus biacanthus, Zhuangodiscus orthacanthus, Zhuangodiscus pentacanthus, Tetratormentum nandanensis, Octatormentum yaoi) and 11 undetermined species. A new radiolarian assemblage, Neoalbaillella camarata Assemblage is proposed, which is located at the upper part of Neoalbaillella optima Assemblage Zone, corresponds well with the Albaillella yaoi Zone.

Remains of a pteranodontid pterosaur are recorded in the basal Austin Group of North Texas. The specimen described here comprises a partial left wing and strongly resembles Pteranodon although diagnostic features of that genus are lacking. With an estimated early Coniacian age, this specimen represents the earliest occurrence of the Pteranodontidae in North America and the second earliest occurrence worldwide, predated only by Ornithostoma from the Cambridge Greensand of England. Pterosaur material recovered from the Eagle Ford and Austin groups of Texas records an early Late Cretaceous change in the composition of North American pterosaur communities between the late Cenomanian and the early Coniacian. This faunal transition appears to be primarily a decrease in morphological disparity rather than a significant reduction in taxonomic diversity. However, the lack of Early Cretaceous Lagerstätten in North America may produce underestimates of true pterosaur richness during this interval, thereby obscuring a subsequent drop in diversity.

Articulated meraspid and holaspid exoskeletons of Guangxiaspis guangxiensis from the Guole Township, Jingxi County, Guangxi Province, China, are preserved in mudstone deposited during an obrution event. The species has a short dorsal pre-cranidial median suture that splits ventrally into a pair of posteriorly divergent connective sutures. The rostral plate of G. guangxiensis is thus triangular in outline, as in the co-occurrent Shergoldia laevigata, which also bore a conterminant hypostome. These two taxa appear to be closely related. The cephalic venter of Shergoldia laevigata has recently been interpreted to suggest a diphyletic origin of the median suture within the order Asaphida, but Guangxiaspis guangxiensis, Shergoldia laevigata and other tsinaniid trilobites display several characters reminiscent of members of the non-asaphide suborder Leiostegiina. These include swellings adjacent to the margins of the L1 glabellar lobe, the shape and furrows of the glabella, a semi-circular pygidium with a long and thin axis, and macrospinous first opisthopleurae of the holaspid pygidium. Based on these characters and on other new information on the early ontogeny of other tsinaniids, all these taxa likely belong within Leiostegiina. This suggests that the median suture arose independently in corynexochide and asaphide trilobites. The degree of convergence between S. laevigata and members of the derived asaphide family Asaphidae was remarkable. Guangxiaspis guangxiensis shows marked morphological change during both meraspid and holaspid ontogeny and might include more than a single morphotype.

We report here the first crustacean microcoprolites from the Sambosan Accretionary Complex (AC) in Japan. Three species of crustacean (order Decapoda) microcoprolites - Payandea japanica n. sp., Favreina tosaensis n. sp., and a species belonging to the genus Parafavreina? sp. are described from the Late Carnian to Rhaetian shallow-water limestones of the Sambosan AC, which were originated on extinct and subsiding volcanoes forming a mid-oceanic atoll-type buildup in the Panthalassan Ocean. Coprolites, which occur within a lagoonal to back-reef facies, provide new insight into the micropaleontology and sedimentology of the Sambosan limestones. Their presence in this tropical shallow-water depositional setting heightens their status of sedimentary facies indicators of such environments. Furthermore the occurrence of these Tethyan coprolites genera in Japan improves our knowledge of the distribution of Triassic crustacean decapods across the Panthalassan Ocean.