Girty (1895) named six species of stromatoporoids from the Lower Devonian of central and east-central New York, which are here redescribed and reillustrated. Additional new specimens provide data on variations within the following species: Anostylostroma jewetti, Parallelostroma foveolatum, ?Parallelostroma centrotum, and ?Parallelostroma microporum.

Styliolina obtusa (Hall, 1879), only known from specimens on two slabs, is placed in synonymy with S. fissurella (Hall, 1843), a ubiquitous fossil in western New York. Styliolina spica (Hall, 1888) is known only from the holotype. This individual is about three times larger than specimens of S. fissurella (Hall); it is removed from the genus. “S.” spica is based on the broken apical end of a calcareous worm tube and is similar to Coleolus. Both of these poorly known taxa were described from different intervals in the Wanakah Shale Member of the Ludlowville Formation near Buffalo, New York.

A new raphistomatinid genus, Wisconsinella, from the Middle Devonian of Wisconsin is described. The type and only known species is Wisconsinella clelandi n. sp. from the Lake Church Formation of late Eifelian age. The new genus is characterized by its highly angular whorl profile and low gradate spire. It is distinguished from all other known raphistomatinid genera by the presence of a narrow, steeply inclined outer whorl surface, demarked both above and below by a sharp, strong angulation.

George Jennings Hinde (1839–1918) was a pioneering geologist and paleontologist. Not only did he contribute greatly to the conodont research field by making innovative studies on Ordovician and Devonian faunas (see e.g., von Bitter, 2004), he was one of the first to describe scolecodonts, the jaws of polychaete worms. Scolecodont publications prior to Hinde's (1879, 1880, 1882, 1896) four contributions were few and merely included descriptions of one or a few specimens. Hinde was aware of the taxonomic affinity of these fossils, a discovery that he ascribed to the Swedish paleontologist Nils Peter Angelin (Hinde, 1882, p. 3–4). Moreover, he was first to investigate these fossils from the world-famous island of Gotland, Sweden (Hinde, 1882), from which most studies on Silurian scolecodonts subsequently have been carried out (Eriksson et al., 2004). Although he understood that the scolecodonts were parts of complex jaw apparatuses, he felt forced to use a single-element-based taxonomy (see Hinde, 1879, p. 373–374). He described close to a hundred “species” and varieties, and many of these names are still in use. Hence, Hinde's scolecodont heritage is still very much alive and his type collections are critical for the study of these fossils, particularly for resolving nomenclatural and taxonomic problems. In this note we discuss, and illustrate for the first time, the graptolites briefly mentioned by Hinde (1879) and describe the important stratigraphic information that they contribute to his Upper Ordovician scolecodont types.

Small fusulinids are common in the Atokan and most Desmoinesian marine units in Ohio but less common in Missourian and Virgilian units. Twenty-one taxa are recognized. Five new species are proposed, including Millerella? elegantula, Eostaffella? recondita, Eostaffella inusitata, Pseudostaffella douglassi, and Pseudoendothyra ohioensis. Several specimens of uncertain taxonomic assignment are also included.

Approximately one-third of the previously recognized taxa were originally described from Europe and about one-half from western North America. Millerella? carbonica Grozdilova and Lebedeva, Eostaffella rjasanensis Rauzer-Chernousova, E. mutabilis Rauzer-Chernousova, and E. acuta Grozdilova and Lebedeva are reported from North America for the first time. The known ranges of several species have been extended significantly. These conclusions support the concept of a greater cosmopolitanism of Pennsylvanian foraminifers than has been generally recognized.

A low diversity fauna of microscopic crinoids from the Kinderhookian (Mississippian) McCraney Limestone at Seehorn Hollow, western Illinois, is described and illustrated by stereomicrographs. The crinoids include first record of the camerate crinoid genus Hexacrinites (H. mississippiensis n. sp.) above the Devonian. The other three taxa are all inadunates and include the monocyclic microcrinoid Allagecrinus mccraneyensis n. sp., which has up to 14 arms, and two dicyclic poteriocrinoids, Hypselocrinus maccabei (Miller and Gurley, 1894) and an indeterminate genus of the Scytalocrinidae.

Rhenopyrgids are rare, turreted edrioasterid edrioasteroids from the lower Paleozoic with a distinctive and apparently conservative morphology. However, new, well-preserved rhenopyrgid edrioasteroid material from Canada, along with a review of described taxa, has revealed broader structural diversity in the oral surface and enabled a re-evaluation of rhenopyrgid functional morphology and paleoecology.

The floor plates in Rhenopyrgus viviani n. sp., R. coronaeformis Rievers, 1961 and, R. flos Klug et al., 2008 are well fused to each other and the interradial oral plate and lack obvious sutures, thereby forming a single compound interradial plate. This differs from other rhenopyrgids where sutures are more apparent. Such fused oral surface construction is only otherwise seen in some derived edrioblastoids and in the cyathocystids, suggesting homoplasy.

Our analysis further suggests that the suboral constriction could contract but the flexible pyrgate zone could not. Thus, specimens apparently lacking a sub-oral constriction should not necessarily be placed in separate genera within the Rhenopyrgidae. It also supports rhenopyrgids as epifaunal mud-stickers with only the bulbous, textured, entire holdfasts (coriaceous sacs) anchored within the substrate rather than as burrow dwellers or encrusters.

Rhenopyrgus viviani n. sp. is described from the Telychian (lower Silurian) Jupiter Formation of Anticosti Island, Québec, Canada and is differentiated by a high degree of morphological variability of pedunculate plates, broader oral plates, and narrower distal ambulacral zones. Specimens lacking or with obscured diagnostic plates from the Ordovician of Montagne Noire, France, and the Ordovician and Silurian of Girvan, Scotland are also described.

UUID: http://zoobank.org/7f81d67f-4155-4719-8a45-b278ad70739d

A new species of Apiocrinites is described from the Middle Jurassic (Callovian) Matmor Formation of the Negev, Israel. Apiocrinites negevensis is from the tropical latitudes in the Tethys, in contrast to all other reported species of this genus. With a narrow radial facet and adjacent arms not in lateral contact and large aboral cup plates, A. negevensis is quite unusual for this genus.

A tooth battery, palatoquadrate, and a gill-arch element of Bobbodus schaefferi were collected from Late Pennsylvanian/Early Permian (Asselian) rocks near Manhattan, Kansas. Depending on the placement of the Pennsylvanian–Permian boundary, this specimen extends the upper limit of the species from the Virgilian (Gzelian) into the Gearyan (Asselian). The new range thus is Kasimovian to Asselian, a 15 my interval. Based on features of the palatoquadrate, the diagnoses of the order Eugeneodontida and the superfamily Caseodontoidea are revised. Bobbodus is the most primitive genus of the order Eugeneodontida.

The early astogeny of specimens representing the bryozoan genera Dekayia, Parvohallopora, Heterotrypa, and Homotrypella follows the same pattern documented in other Ordovician trepostomes. After larval settlement and metamorphosis, typically three primary, periancestrular, autozooids bud distally from the founder zooid, the ancestrula, with secondary zooids budding from the primaries, tertiary zooids from the secondaries, and so on. Progressive lateral displacement of buds, through backbudding, eventually produces a subcircular ancestrular disk. Significant intergeneric differences in this basic pattern do not appear to exist. Intrageneric variability in budding pattern occurs during colony development. That variability might have resulted from any or all of the following sources: within-genus plasticity, the development of multiple ancestrulae, or environmental variation. The basic pattern of three primary buds developed from individual ancestrulae has been recognized in other trepostomes, some cyclostomes, and two suborders of cryptostomes. Cladistically, the trait must be considered polyphyletic until more is known about the number of primary buds in the remaining bryozoan suborders. Ancestrular dimensions are statistically similar across genera except between the smaller Dekayia and larger Parvohallopora, but ancestrular sizes in all four Dillsboro genera are consistent with the inference that they possessed a polyembryonic lecithotrophic larval type.

Large palaeotrochid gastropods of the genera Floyda Webster (1905a) and Turbonopsis Grabau and Shimer (1909) occur in the late Frasnian Lime Creek Formation of Iowa. Floyda concentrica was designated as the type species of Floyda by earlier workers (Webster, 1905a; Knight, 1941), but is a junior synonym of F. gigantea (Hall and Whitfield, 1873). Three of five species and subspecies of Floyda described from the Lime Creek (Floyda concentrica, F. concentrica multisinuata, and F. gigantea depressa) are considered synonyms of the type species F. gigantea; the fifth species, F. gigantea hackberryensis, is here reassigned to the closely related genus Turbonopsis. Both F. gigantea and T. hackberryensis are redescribed using the original types and additional hypotype material from the collections of Charles Belanski.

Floyda, first known from late Givetian rocks of the Rhenish Slate Mountains in Germany, is widespread in the United States Midcontinent and western North America by early Late Devonian time. Turbonopsis was endemic to the Appohimchi Subregion of the Eastern Americas Realm prior to the Taghanic Onlap, and appears to have remained so until late Frasnian time when it migrated to western North America.

Eustatic sea-level highstands during the Middle and Late Devonian are thought to have breached barriers to migration, allowing both Floyda and Turbonopsis to disperse by prevailing oceanic currents from the United States Midcontinent into western North America during the late Frasnian. The expected oceanic current patterns of the Middle and Late Devonian paleogeographic reconstructions of Heckel and Witzke (1979, figs. 3, 5) adequately account for the known distribution and dispersal of Devonian palaeotrochid gastropods.

The Palaeotrochidae underwent extinction prior to the latest Frasnian. Floyda, Turbonopsis, and Westerna became extinct during the onset of the last eustatic deepening event prior to the close of the Frasnian. The extinction of the palaeotrochid gastropods as well as other invertebrate groups may have been the result of restriction or near elimination of shallow warm-water, well-oxygenated shelf habitats by the onlap of cold anoxic bottom waters prior to latest Frasnian time.

The use of different methodological approaches together with an exhaustive qualitative study has helped to recognize important morphological traits to distinguish species in a systematic and phylogenetic framework. Parabolinella triarthroides Harrington, 1938 was described based on two cranidia from the Quebrada de Coquena, Purmamarca, Jujuy province. The generic assignment of P. triarthroides has been questioned by a phylogenetic analysis, which resolves this species as the sister group of Bienvillia Clark, 1924. To explore the generic assignment of this species, a revision of the type material, plus a morphometric analysis including specimens of Parabolinella Brøgger, 1882 and Bienvillia were performed. In addition, the original matrix used in the published phylogeny was reviewed and enlarged, including more species of Bienvillia. Continuous characters were coded in different ways in order to compare how they could affect the ordering of specimens and their phylogenetic relationships. Finally, both methodologies were compared, especially in regard to the behavior of the quantitative characters included in the analyses. From the combined analyses, it is shown that similarities between the cranidium of P. triarthroides and all other Parabolinella species are true homologies instead of a by-product of evolutionary convergence. Therefore, P. triarthroides should be considered a member of this genus. Finally, this study demonstrates that the best strategy for solving systematic problems in groups where the morphological variation is the only source of information (i.e., fossil taxa without living representatives) is the implementation of an integrative approach, combining different methodological techniques and a good description of specimens.

Fossil insects from the Triassic-Jurassic boundary of England could provide an important resource for investigating the severity of extinction events in the terrestrial realm of the uppermost Triassic. However, the fossil record is poorly understood for this period even though there are abundant historical collections. Many of these collections are still in need of taxonomic revision before they can be used to reconstruct past entomofaunas and make inferences about diversity change through time. This paper is part of a larger project to revise the taxonomy of insects across the Triassic-Jurassic boundary of England to better understand changes in insect diversity through the Triassic-Jurassic boundary and associated extinction period. Herein, the damsel-dragonfly family Liassophlebiidae Tillyard, 1925 is revised and an additional specimen from the Early Jurassic of Antarctica is included. Rossiphlebia new genus is erected for Liassophlebia jacksoni Zeuner, 1962; L. batheri Tillyard, 1925 is considered nomen dubium and another specimen originally attributed to L. batheri is identified as L. withersi Tillyard, 1925. Liassophlebia (?) clavigaster Tillyard, 1925 and L. (?) hopei (Brodie, 1845) are considered incertae sedis at the generic level. Liassophlebia gigantea Zeuner, 1962 is based on a fragmentary specimen but has several unique key characteristics. We redescribe it in Anglophlebia new genus and tentatively in Anglophlebiidae new family in Heterophlebioptera. Also discussed are L. magnifica Tillyard, 1925, L. withersi, and L. pseudomagnifica Whalley, 1985, which are redescribed with updated figures. Caraphlebia antarctica Carpenter, 1969 was originally described from the Early Jurassic of Antarctica as being closely related to Liassophlebia; it is herein confirmed in Selenothemistidae Handlirsch, 1939.

UUID: http://zoobank.org/8fe9a39c-1c3b-4bda-92a6-92c1a0fc95b8

Two recently collected specimens of Bogotacrinus scheibei Schmidt, 1937, from the Devonian (Emsian–Eifelian) Floresta Formation of Colombia reveal that Bogotacrinus is a dicyclic camerate crinoid genus closely related to Pterinocrinus Goldring, 1923 (Lower–Upper Devonian of eastern North America and western Europe), and Ampurocrinus McIntosh, 1981 (Lower Devonian of Bolivia). The new diplobathrid camerate crinoid family Pterinocrinidae, characterized by species with low conical dicyclic cups and rami composed of compound, bipinnulate brachials, is herein proposed to accommodate these three genera. This family originated in western Europe and migrated into the Malvinokaffric and southern Eastern Americas Realms during the Early Devonian and into the northeastern Appalachian Basin by the Late Devonian.

The recently discovered mass mortality of fishes from the Tanis Site in the North Dakota portion of the Late Cretaceous Hell Creek Formation contains many well-preserved, three-dimensional skeletons. Among these are representatives of two acipenseriform families, Acipenseridae (sturgeons) and Polyodontidae (paddlefishes). This paper describes two new monotypic polyodontid genera, expanding our knowledge of polyodontid diversity. The first of the new species described here is †Parapsephurus willybemisi n. gen. n. sp. It is distinguished from all other known species by having a combination of posteriorly elongate parietals, the middle fenestra longitudinalis bordered medially by the parietal and frontal and laterally by the dermopterotic, slender and numerous dorsal caudal fulcra, an elongate hyomandibula that is not hourglass shaped, and gill rakers that are short and widely spaced. The second polyodontid species described here is †Pugiopsephurus inundatus n. gen. n. sp. It is diagnosed by a combination of having stellate bones that are exceptionally poorly developed or absent and having a dermopalatine with a medial expansion and lacking an ectopterygoid process. The two species of paddlefishes described in this paper add to the morphological and taxonomic diversity of Polyodontidae. The presence of these taxa within the Hell Creek Formation hints at substantial diversity of polyodontids at this stage of their evolutionary history.

UUID: http://zoobank.org/08cbf8c5-59ba-41fa-9265-8cb762cf7b13

As many as eight species of the “anchitherine” equid Miohippus have been identified from the John Day Formation of Oregon, but no statistical analysis of variation in these horses has yet been conducted to determine if that level of diversity is warranted. Variation of the anterior-posterior length and transverse width of upper and lower teeth of Turtle Cove Member Miohippus was compared to that of M. equinanus, Mesohippus bairdii, Equus quagga, and Tapirus terrestris using t tests of their coefficients of variation (V). None of the t tests are significant, indicating that the variation seen in Turtle Cove Miohippus is not significantly different from any of the populations of other perissodactyls examined in this study. Data also indicate that Mesohippus is present in the Turtle Cove Member. Additionally, hypostyle condition, used to diagnose all species of Miohippus, was found to be related to stage of wear using an ordered logistic regression. Only two species of equid, one Miohippus and one Mesohippus, in the Turtle Cove Member can be identified, therefore only Miohippus annectens, the genotype and first species described from the region, can be recognized as the sole Miohippus species known from the Turtle Cove assemblage. There are insufficient data to determine which species of Mesohippus is present. The dependence of hypostyle condition on crown height in Miohippus implies that wear stage must also be considered in investigations of dental morphology in the “Anchitheriinae.”

Toyotamaphimeia is an extinct crocodylian lineage whose name is derived from a mythological Japanese princess. Here, we re-examine the type specimens of a long-forgotten species: Tomistoma taiwanicus from the Pleistocene of Tainan (Taiwan) and revise its taxonomic status to Toyotamaphimeia taiwanicus n. comb., leading to the first recognized species of Toyotamaphimeia outside Japan. Our phylogenetic analyses also support this taxonomic assignment and, more interestingly, further suggest an East Asian lineage. In addition, Toyotamaphimeia taiwanicus n. comb. represents a tropical species, resolving a long-standing puzzle of why Toyotamaphimeia only inhabited a much higher latitudinal area (Japan). Given the large body size of Toyotamaphimeia taiwanicus n. comb. (~7 m) and the fact that it is geologically older than Toyotamaphimeia machikanensis from Japan, we propose a novel evolutionary scenario: the genus Toyotamaphimeia originated in Taiwan and evolved to a large body size with gigantothermic physiology, which resulted in migration out of Taiwan and dispersal farther north to Japan. Our taxonomic identification shows the presence of an extinct endemic crocodylian species from the Pleistocene of Taiwan with large-scale paleogeographic implications. This study, with our recent progress in vertebrate paleontology in Taiwan, should provoke more in-depth paleontological research on the Pleistocene extinction.

Two rare, phosphatized, tubular microfossils of uncertain affinity, probably algal, are described from the Portfjeld biota (Ediacaran) of North Greenland. Portfjeldia aestatis n. gen. n. sp. preserves two tubules, one of which branches, within an annulated outer sheath. Its morphology can be compared to that of the much larger Ramitubus from the Weng'an biota of South China. An unnamed long, parallel-sided tubule occupied the postmortal cavity formed within diagenetically mineralized specimens of the cyanobacterium Jiangispirellus.

Family-level taxonomic concepts for Paleozoic Asteroidea are problematic; data availability for the family Urasterellidae, however, is judged sufficient for familial reappraisal. The survey cannot be fully comprehensive because certain available names are founded on very limited material, with specimens widely scattered among collections. Recognized urasterellid genera include Urasterella Schuchert, 1914; Anthroosasterias Blake, 2017; Meturaster Blake, Guensburg, and Lefebvre, 2016; Salteraster Stürtz, 1893; Staurasterias Blake, 2017; Ulrichaster Spencer, 1950; and Pegoasterella pompom n. gen. n. sp. Other available generic names are held in abeyance. The name Urasterella has approached form-genus status, an outcome exacerbated by incomplete understanding of the type species. Urasterella huxleyi (Billings, 1865) is reassigned to Anthroosasterias. Relatively large specimen suites for Anthroosasterias huxleyi (Billings, 1865) and Salteraster grandis (Meek, 1872) enable some interpretation of urasterellid intrataxon variation, ontogenetic change, and life mode. Morphologic changes accompanying ontogeny of A. huxleyi are argued as favoring a shift from substrate surface feeding to feeding through extension of arms into the water column in a manner comparable to that seen among extant Forcipulatida and ophiurans.

UUID: http://zoobank.org/82d2eca7-55e0-42ed-a164-c666652e3972