Radiodontan body elements, some belonging to Peytoia and Hurdia and some unassigned, have been reported from the Langston Formation (Spence Shale Member), Wheeler Formation, and Marjum Formation of the middle Cambrian (Series 3) of Utah. These identifications are reassessed in light of recent work on the morphology of the radiodontan Hurdia. New specimens of Hurdia are identified from the Spence Shale, representing mouthparts (oral cones), cephalic carapace H-elements, frontal appendages, and a single isolated swimming flap. The shape of the H-elements allows H. victoria Walcott, 1912 to be identified from the Spence Shale for the first time. The flap is larger and more complete than any reported from the Burgess Shale and allows for a better understanding of the morphology of Hurdia swimming flaps. A 3D model of a Hurdia frontal appendage indicates that there is only one morph of Hurdia frontal appendage found in both species, and apparent morphological differences between disarticulated appendages reflect a preservational continuum caused by varying oblique angles relative to the seafloor. Peytoia should no longer be reported from the Spence Shale, but its presence is confirmed in the Wheeler and Marjum formations. New mouthparts (oral cones) of Hurdia from the Spence Shale and Peytoia from the Marjum Formation with surface textures of submillimeter-diameter raised nodes are described. These new features have not been observed in material from the Burgess Shale and suggest slight differences in preservation.

New shell material of a trionychid turtle from the Upper Cretaceous (upper Campanian) Fossil Forest Member of the Fruitland Formation of northwestern New Mexico represents a new species, Gilmoremys gettyspherensis. The material consists of right costals I–III, V, VI, and VIII, left costals V, VII, and VIII, the left half of the entoplastron, the right hypo- and xiphiplastron, and the left hyo-, hypo-, and xiphiplastron. The specimen shows great similarities to the Late Cretaceous (Maastrichtian) trionychid Gilmoremys lancensis (Gilmore, 1916) by having a relatively thin shell, carapacial sculpturing consisting of fine pits combined with extended sinusoidal ridges or grooves, free costal rib ends, presence of a preneural, a distally constricted costal I and distally expanded costal II, two lateral hyoplastral processes, low hyoplastral shoulders, and full midline contact of the elongate xiphiplastra, but differs by being smaller, having raised sinusoidal ridges on the carapace instead of grooves, less distally expanded costals II, and less elongate xiphiplastra. Phylogenetic analysis places Gilmoremys gettyspherensis n. sp. as sister to Gilmoremys lancensis near the base of the clade Plastomenidae. Like the majority of previously described plastomenid materials, the type specimen of Gilmoremys gettyspherensis n. sp. was collected from a mudstone horizon, suggesting a preference for ponded environments.

UUID: http://zoobank.org/e7165061-d86b-46b7-a1f8-c31f5a8ed628

Medusaceratops lokii Ryan, Russell, and Hartman, 2010 is an enigmatic taxon of ceratopsid represented by partial parietals from the Mansfield bonebed in the Campanian Judith River Formation, Montana. Originally, all ceratopsid material collected from this bonebed was referred to the centrosaurine ceratopsid Albertaceratops, but subsequently two parietals were designated the types of the chasmosaurine, M. lokii, in part, because they were interpreted to have three epiparietals bilaterally. Here we describe new material from the bonebed that allows a systematic revision of the taxon. A revised reconstruction of the frill, informed by newly discovered parietals, reveals that M. lokii had a broad midline ramus and at least five epiparietals (ep) around the margin of the frill, both traits that are characteristic of Centrosaurinae. From medial to lateral, the epiparietal ornamentation consists of a small, variably procurving epiparietal (ep 1), an anterolaterally curving pachyostotic hook (ep 2), a smaller pachyostoic process (ep 3), and two small triangular epiparietals (ep 4 and 5). A phylogenetic analysis of ceratopsids, which is the first to include Medusaceratops, indicates that M. lokii is a unique, early centrosaurine ceratopsid taxon that is more closely related to Centrosaurini and Pachyrhinosaurini than Nasutoceratopsini. No unequivocal chasmosaurine bones or diagnostic material from any other ceratopsid could be identified from the Mansfield bonebed, suggesting that it represents one of the oldest occurrences of a monodominant accumulation of a centrosaurine ceratopsid on record.

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.

UUID: http://zoobank.org/e3e268a7-88e5-43cd-84ea-b40df45e8281

Misidentified fossils are common in paleontology, but Platylithophycus has undergone a particularly problematic series of descriptions. The holotype of P. cretaceus comes from the Upper Cretaceous Niobrara Chalk of Kansas, and was first described as a calcareous green alga, based on the surface texture of the specimen. Later, Platylithophycus was re-identified as a sepiid cephalopod, based partly on a comparison of microstructure between P. cretaceus and the pen of modern squids. Platylithophycus then became part of the University of Nebraska teaching collection, where, according to paleontological legend, an undergraduate student suggested that the fossil’s tessellated surface looked a lot like shark cartilage. However, that interpretation has not been formally proposed until now. This work re-describes the holotype of Platylithophycus cretaceus as part of the branchial endoskeleton of an elasmobranch, based on both gross morphology and ultrastructure, including recognizable tessellated cartilage with intertesseral pores and joints.

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.

UUID: http://zoobank.org/ca8e0023-7c9d-4b00-a294-d166c37c5c71

The Leptarctinae are an enigmatic subfamily of mustelids present in North America and Eurasia during the Miocene (Arikareean to Hemphillian North American Land Mammal Ages). Their diet and ecology have been particularly controversial. Some workers have suggested they were similar to koalas, whereas others suggested they were crushing omnivores analogous to raccoons. Leptarctus oregonensis Stock, 1930, a poorly known leptarctine from the early Barstovian, is represented by fragmented cranial elements and isolated teeth from the Mascall Formation of Oregon, and some fairly complete but undescribed material from the Olcott Formation of western Nebraska. Herein, we describe the first well-preserved skull of L. oregonensis from the type formation. Based on this new specimen, we confirm that L. oregonensis is a distinct species from L. primus Leidy, 1856 and L. ancipidens White, 1941 that is characterized by a distinct morphology of its tympanic projections and first upper molars. We are also able to describe intraspecific variation within L. oregonensis coinciding with the geographic distribution of the specimens (Oregon and Nebraska). The most variable characters are concentrated in the morphology of the frontals and the upper fourth premolar. Additional specimens will be needed to settle the debate over sexual dimorphism in this species, but this new specimen suggests that Leptarctus oregonensis, despite being one of the smallest members of the Leptarctinae, was an animal-dominated omnivore with considerable crushing ability.

The Cretaceous landmass of Appalachia has preserved an understudied but nevertheless important record of dinosaurs that has recently come under some attention. In the past few years, the vertebrate faunas of several Appalachian sites have been described. One such locality, the Ellisdale site of the Cretaceous Marshalltown Formation of New Jersey, has produced hundreds of remains assignable to dinosaurs, including those of hadrosauroids of several size classes, indeterminate ornithopods, indeterminate theropods, the teeth, cranial, and appendicular elements of dromaeosaurids, ornithomimosaurians, and tyrannosauroids, and an extensive microvertebrate assemblage. The theropod dinosaur record of the Ellisdale site is currently the most extensive and diverse known from the Campanian of Appalachia. Study of the Ellisdale theropod specimens suggests that at least four or more non-avian theropod taxa are represented at the site, including tyrannosauroids, ornithomimosaurs, several different morphotypes of dromaeosaurids that are the first of that clade described from New Jersey, and indeterminate theropods. The specimens are important for increasing current knowledge about the theropod diversity of the Atlantic Coastal Plain (ACP) during the Campanian by representing the most speciose assemblage of the group during the time in the ACP as well as for shedding light on Appalachian dinosaur ecology and biogeography generally.

Bison antiquus Leidy, 1852 was one of the largest and most widely distributed megafaunal species during the Late Pleistocene in North America, giving rise to the modern plains bison in the middle Holocene. Despite the importance of the ancient bison, little is known about its feeding ecology. We employed a combination of extended mesowear, and mesowear III to infer the dietary preference and habitat use of three Mexican samples of B. antiquus. These included two northern samples—La Piedad-Santa Ana and La Cinta-Portalitos—from the Transmexican Volcanic Belt morphotectonic Province, as well as one southern sample—Viko Vijin—from the Sierra Madre del Sur morphotectonic province. We found that the northern Mexican samples were primarily nonstrict grazers, whereas the southern sample displays a pattern consistent with mixed feeding habits. This suggests variability among the diets of the bison from these samples, caused by different paleoenvironments. This evidence complements the paleoenvironmental reconstructions in the studied localities; for the northern samples, open prairies composed of patches of woodland or shrubland and, for the southern locality, a fluvial floodplain with short-lived vegetation. In both scenarios, grasses (Poaceae) were nondominant. The dietary habits of our samples of ancient bison in Mexico are the southernmost dietary inference for the species in North America and expand our knowledge of the dietary habits of B. antiquus during the Late Pleistocene.

The partial skull of a lion from Natodomeri, northwest Kenya is described. The Natodomeri sites are correlated with Member I of the Kibish Formation, dated to between 195 ka and ca. 205 ka. The skull is remarkable for its very great size, equivalent to the largest cave lions (Panthera spelaea [Goldfuss, 1810]) of Pleistocene Eurasia and much larger than any previously known lion from Africa, living or fossil. We hypothesize that this individual represents a previously unknown population or subspecies of lion present in the late Middle and Late Pleistocene of eastern Africa rather than being an indication of climate-driven size increase in lions of that time. This raises questions regarding the extent of our understanding of the pattern and causes of lion evolution in the Late Pleistocene.