The genus Neocricetodon represents one of the most diverse radiations of extinct cricetines. Its early evolution remains unclear, mainly owing to the incomplete fossil record. One of the earliest and least known species of this genus is N. moldavicus described from the early late Miocene localities Bujor 1 and Calfa, Moldova. We reexamined the type material of this species and compared it with other species of Neocricetodon. Despite its old geological age, N. moldavicus demonstrates rather advanced dental morphology including the anterocone of M1 being deeply split; mesolophs and mesolophids partially reduced; and the labial spur of the anterolophule, ectomesolophids, and lingual anterolophid of m2 lacking. The phylogenetic analysis of 15 Neocricetodon species based on 22 dental characters revealed three synapomorphies for the genus: presence of the M1 labial anterolophule, the four-rooted M2, and presence of the labial anterolophulid of m1. “Kowalskia cf. schaubi” from Rudabánya and “Kowalskia sp.” from Vösendorf, formerly considered as the earliest finds of Neocricetodon, do not possess these characters and rather represent the genus Democricetodon. Our study also suggests that Kowalskia complicidens is a member of Sinocricetus, and that N. neimengensis and N. zhengi are junior synonyms of N. polonicus. The recognition of N. moldavicus as the earliest member of the genus within the clade containing the species of Neocricetodon from France and Spain supports the hypothesis of the Eastern European origin of the Western European Neocricetodon species.

Two regional composite sections in the Frasnian, Upper Devonian, of New York State result from graphic correlation of conodont species. The first extends from Frasnian conodont zones 3 to 7, the second from Frasnian zones 11 to 13c (we prefer this terminology to “Montagne Noire” or “MN” zonation as the zone-defining species occur throughout the Devonian tropics). Key beds, widely traceable bases of prominent black shales, have been used with only a few exceptions to position the lines of correlation (LOC) in the graphs. Other key beds, not used for positioning, fall exactly on the LOC supporting the hypothesis of their synchrony. Fifty-five conodont species in the New York regional composites are compared with their ranges in the global Frasnian Composite Standard proving no major discrepancies. The taxonomy of Ancyrodella nodosa Ulrich and Bassler, widely misidentified in the past, has been clarified through restudy of the type specimens, resulting in its distinction from A. hamata Ulrich and Bassler (=A. buckeyensis Stauffer). A new species of Polygnathellus Bassler, which is restricted to Frasnian Zone 4, is kept in open nomenclature because the rarity of specimens is insufficient to determine the extent of intraspecifc variation and whether one or two species are represented in our New York and Western Australian collections.

The holotype partial skull of Agorophius pygmaeus (the monotypic form for both the genus Agorophius and the Family Agorophiidae) has been missing for approximately 140 years. Since the discovery of Agorophius pygmaeus, many additional taxa and specimens have been placed in the Family Agorophiidae, only to be reclassified and removed later. This has created confusion as to what is and what is not an agorophiid and a lack of clarity as to what characteristics delimit the Agorophiidae. A newly discovered skull of an agorophiid recently collected from an underwater cliff face of the Ashley River, South Carolina, USA, is assigned to Agorophius pygmaeus. It derives from the base of the Ashley Formation (early Oligocene). The new specimen consists of most of the skull and periotics, which are well preserved and described for the first time in an agorophiid. The new specimen provides an opportunity to diagnose the Agorophiidae and place the genus and species within the phylogenetic context of the early odontocete radiation in the Oligocene, along with other taxa such as the Ashleycetidae, Mirocetidae, Patriocetidae, Simocetidae, Waipatiidae, and Xenorophidae. Based on this new understanding, Agorophiidae are known with certainty only from the early Oligocene of South Carolina, with other undescribed, potential agorophiid specimens from the Oligocene of the North Pacific region (Japan, Mexico, and Washington State).

Rare remains of hadrosaurian dinosaurs previously reported from the Maastrichtian Javelina Formation of West Texas had been attributed tentatively to either Edmontosaurus or Kritosaurus. Three recently recovered specimens include substantial skull parts and postcranial skeletal elements sufficient to recognize three distinct hadrosaurs. Two species are found in the lower part of the Javelina Formation; one of these is identified as Kritosaurus sp., confirming the earlier referral of specimens to this taxon. The most complete of these specimens combines features thought to be diagnostic of both K. navajovius Brown, 1910 and ‘Naashoibitosaurus’ ostromi Hunt and Lucas, 1993 and exhibits some unique attributes such that its specific identity remains uncertain. A second species, documented by a single specimen found near the base of the Javelina Formation, is inadequate to confidently identify but appears to represent a ‘solid-crested’ saurolophine with frontals having upturned processes along the midline, similar to those that brace the posterior side of the narial crest in Saurolophus. A third hadrosaur is represented at a bonebed in the uppermost part of the Javelina Formation. Its remains are sufficient to justify designation as a new species ?Gryposaurus alsatei. The skull roof elements are similar to those in species of Gryposaurus, and although no parts of the narial crest are preserved, the bordering elements indicate that ?G. alsatei was a ‘flat-headed’ saurolophine. Referral of ?G. alsatei to Gryposaurus would constitute a significant temporal range extension for the genus into late Maastrichtian time, and if correct, this long-lived lineage of hadrosaurs persisted nearly to the end of Cretaceous time in West Texas. ?G. alsatei was a contemporary of Edmontosaurus, the sole terminal Cretaceous hadrosaur in the northern Great Plains region, and neither possessed the ornate narial crest that characterized many earlier hadrosaurs.

The Actinocrinitidae were among the most abundant crinoids worldwide during the Lower Mississippian. Recent systematic revisions of the family allow a revised genus- and species-level understanding of these crinoids globally and a more precise means by which to understand the temporal and facies distribution of genera and species in this important Mississippian family. Two genera with a total of five species of Actinocrinitidae (and five additional forms left in open nomenclature) are recognized from the Fort Payne Formation, including Actinocrinites jugosus (Hall, 1859), Actinocrinites spp. indeterminate, Thinocrinus gibsoni (Miller and Gurley, 1893), Thinocrinus lowei (Hall, 1858), Thinocrinus probolos (Ausich and Kammer, 1991), Thinocrinus akanthos new species, Thinocrinus sp. aff. T. gibsoni, Thinocrinus spp. indeterminate, and two taxa recognized as only Actinocrinitidae genus and species indeterminate. Actinocrinites tripus Ehlers and Kesling, 1963 is recognized as a junior synonym of Thinocrinus gibsoni. Thinocrinus, rather than Actinocrinites as previously thought, is the dominant Fort Payne Formation actinocrinitid. Fort Payne Formation carbonate buildup facies (wackestone buildups and crinoidal packstone buildups) each have characteristic species of Thinocrinus. Actinocrinites is relatively rare in the Fort Payne Formation, but occurs preferentially in crinoidal packstone buildups.

New ornithischian remains reported here (MPEF-PV 3826) include two complete metatarsi with associated phalanges and caudal vertebrae, from the late Toarcian levels of the Cañadón Asfalto Formation. We conclude that these fossil remains represent a bipedal heterodontosaurid but lack diagnostic characters to identify them at the species level, although they probably represent remains of Manidens condorensis, known from the same locality. Histological features suggest a subadult ontogenetic stage for the individual. A cluster analysis based on pedal measurements identifies similarities of this specimen with heterodontosaurid taxa and the inclusion of the new material in a phylogenetic analysis with expanded character sampling on pedal remains confirms the described specimen as a heterodontosaurid. Finally, uncommon features of the digits (length proportions among nonungual phalanges of digit III, and claw features) are also quantitatively compared to several ornithischians, theropods, and birds, suggesting that this may represent a bipedal cursorial heterodontosaurid with gracile and grasping feet and long digits. In particular, the elongated non-terminal pedal phalanges and morphology of digit III resemble features present in arboreal birds, a unique condition found so far among ornithischians.

A new Late Jurassic (Oxfordian) asteroid (Echinodermata) faunule from the Swift Formation of Montana includes representatives of four genera including the new genus and species Atalopegaster gundersoni (Stichasteridae), Eokainaster sp. indet. (Astropectinidae), an indeterminate probable member of the Goniasteridae, and a species indeterminate beyond the class level. Because of weathering at the outcrop, preservation is poor.

Although representing an unusual depositional occurrence, overall faunule composition appears comparable to that found in a similar modern environment. The faunule is comparable in age and regional location to earlier Jurassic asteroid discoveries, suggesting wide distribution during a geologically brief time interval of favorable conditions. Asteroids are only rarely reported from the Mesozoic of the North American continental interior, and co-occurrence of multiple fossil taxa is unusual on a global basis.

Recent work on new anthracothere (Mammalia, Artiodactyla) specimens from the Jebel Qatrani Formation, early Oligocene, Fayum, Egypt, has revealed the presence of a new genus. Nabotherium new genus is described on the basis of a partial skull, several mandibular and maxillary specimens, and isolated teeth. The new genus exhibits a distinctive combination of features not seen in other Paleogene anthracotheres. The most noticeable characteristics of the new genus include the presence of large and well-developed upper and lower canines, caniniform third incisors, the presence of only a short diastema between the canine and first premolar, and broad, bunodont cheek teeth. This is in contrast to other contemporary anthracotheres, including other forms from the Fayum, which show a spatulate third incisor, a reduced canine, a much longer canine-premolar diastema, and more narrow, bunoselenodont cheek teeth. The presence of a relatively short rostrum with closely packed incisors, low-crowned and simple premolars, and low-crowned, bunodont molars indicates that members of the new genus would have been more efficient at crushing foods than slicing vegetation, and suggests a more varied herbivorous and frugivorous diet than was favored by other, more bunoselenodont Fayum anthracotheres.

Bathornis (“Neocathartes”) grallator (Wetmore, 1944) from the middle Eocene of Wyoming is based on a partial skeleton, which is the most substantial record of the North American Bathornithidae and one of the most complete fossils of a Paleogene stem group representative of the Cariamiformes. So far, however, an assessment of the evolutionary significance of this important fossil has been hampered by the limited published osteological data. Moreover, cariamiform affinities of B. grallator and its true “genus”-level identity were recognized after the last comprehensive revision of the Bathornithidae, and some of its features were incorrectly portrayed in the original description. Here, the B. grallator holotype is restudied and the taxonomic composition and phylogenetic affinities of bathornithids are revised. It is suggested to restrict Bathornithidae to the taxon Bathornis, from which the putative bathornithid Paracrax differs in numerous features, with even cariamiform affinities of this latter taxon not having been established beyond doubt. B. grallator was a flightless bird and has recently been hypothesized to be the sister taxon of the likewise flightless South American Phorusrhacidae. The present analysis, however, supports a position outside a clade including Phorusrhacidae and Cariamidae (the cariamiform crown clade). Owing to their terrestrial way of living, Cariamiformes appear to have been prone to a loss of flight capabilities. B. grallator shows close similarities to a flightless cariamiform bird from the Paleogene of Europe, but the phylogenetic significance of this resemblance is difficult to assess owing to the limited material known of the latter species.

The Pleistocene fossil sloth Australonyx aquae De Iuliis, Cartelle, and Pujos, 2009 (Mammalia, Xenarthra, Megalonychidae) was described from the intertropical region of Brazil. However, its mandible was not known and only cursory descriptions of the ear ossicles were included. The mandible was subsequently recognized among the remains originally collected from the type locality, and belongs to the holotype individual. As a particularly important skeletal element for specific recognition, it requires description to complement our understanding of this species. The ossicles, usually poorly represented in the fossil record, require further description to allow differentiation from those of other sloths. Comparisons of the mandible and ossicles are conducted with homologous elements of the contemporaneous and sympatric Ahytherium aureum Cartelle, De Iuliis, and Pujos, 2008, the only other megalonychid sloth known from intertropical Brazil, and reinforce the distinction between these two species detailed in their initial descriptions. Comparisons with other sloths (e.g., Acratocnus, Megalonyx, Neocnus) also reveal differences with Au. aquae in such features as form and size of the caniniform tooth, angular process, and mandibular condyle. Differences among the malleus and incus of Au. aquae and several species of other sloth clades reveal clade level distinctions among Megatheriidae, Nothrotheriidae, and Megalonychidae. A well-preserved skull from the Brazilian state of Rondônia is noted as probably belonging to Au. aquae. This skull cannot be assigned formally to this species because it is not deposited in a recognized institution, but it does extend considerably the known range of the species.

A co-occurrence of the ichnogenus Phymatoderma and a star-shaped horizontal trace fossil was discovered from Neogene deep-marine deposits (Misaki Formation, central Japan), and is described herein for the first time. Phymatoderma consists of a straight to slightly curved tunnel that shows first- or second-order branches. The tunnels are 5.30–27.25 mm in diameter and are filled with ellipsoidal pellets. The relatively well-preserved star-shaped trace fossil is a large horizontal structure (~18 cm×19 cm) that consists of at least 10 spokes with diameters ranging from 11.49–20.96 mm. As compared to modern analogous surface-feeding traces produced by abyssal echiuran worms and their burrow morphology, it is highly likely that the star-shaped trace fossil and Phymatoderma found from the Misaki Formation are feeding and fecal traces of ancient deep-sea echiurans, respectively. Difference in preservation potential between surface and subsurface traces may result in rare occurrence of star-shaped trace fossils as compared to Phymatoderma. Microscopic observation of the pelletal infill of Phymatoderma also reveals that the trace-maker fed on organic debris and microorganisms such as diatoms and radiolaria.

The Otariidae (fur seals and sea lions) are an important and highly visible component of Southern Hemisphere marine mammal faunas. However, fossil material of Southern Hemisphere otariids is comparatively rare and often fragmentary. One exception is the Pleistocene sea lion Neophoca palatina King, 1983a, which is known from a nearly complete skull from the North Island of New Zealand. However, the phylogenetic affinities of this taxon are poorly known, and comparisons with other taxa have been limited. We provide an extensive redescription of Neophoca palatina and diagnose this taxon using a morphometric approach. Twenty measurements of the skull were collected for N. palatina, as well as for all extant Australasian otariids and several fossil Neophoca cinerea Perón, 1816. Using principal component analysis, we were able to segregate taxa by genus, and N. palatina was found to cluster with Neophoca according to overall size of the skull as well as increased width of the intertemporal constriction and interorbital region. N. palatina can be distinguished from all other Australasian otariids by its unusually broad basisphenoid. Discriminant function analysis supported referral of Neophoca palatina to Neophoca with very high posterior probability. These results confirm the treatment of Neophoca palatina as a distinct species of Neophoca and highlight the former broad distribution and greater tolerance for colder temperatures of this genus. These results also suggest that New Zealand may have played a pivotal role in the diversification of Southern Hemisphere otariid seals.

The present study of the Eifelian icriodid conodonts is based on collections from Belarus and the Michigan Basin (USA). It is here proposed that forms originally included in Icriodus orri Klapper and Barrick, 1983 can be attributed to I. retrodepressus Bultynck, 1970, Icriodus orri sensu stricto, and Icriodus michiganus new species, each displaying a distinct morphology, stratigraphical range, and geographic distribution. Icriodus retrodepressus, characterized by a triangular spindle, deep depression in its posterior part, and a well-pronounced spur and antispur, appeared in the lower partitus Zone of the lowermost Eifelian and disappeared in the upper Eifelian kockelianus Zone. Icriodus michiganus n. sp., distinguished by a lachrymiform spindle with a shallow posterior depression, ranges from the lower costatus Zone to the upper kockelianus Zone. Icriodus orri differs from the other two species by the occurrence of transverse denticle rows with lateral denticles displaying sharp edges. It ranges from the upper kockelianus Zone to the ensensis Zone of the uppermost Eifelian. Icriodus retrodepressus first occurred in the European part of the Euramerican continent and later migrated into the North American area. Icriodus michiganus n. sp. has been found in the interior part of the North American Craton and near the eastern Euramerican margin. Icriodus orri occurs in the North American interior, in British Columbia (Canada), and in the eastern part of Euramerica (Belarus). The introduction of I. retrodepressus can be related to the transgressive Choteč Event, whereas that of I. orri to a transgressive stage of the Ie eustatic cycle.