This newly described chondrichthyan fauna from the late Miocene Chucunaque Formation of Lago Bayano reveals a prolific and highly diverse assemblage from Panama, and one of the richest shark faunas from the Neotropics. Strontium geochronology indicates an age of 10–9.5 Ma for the chonrichthyan-bearing strata. Field efforts resulted in 1429 identifiable specimens comprising at least 31 taxa, of which at least eight are new to the documented fossil record of Panama. With this information an analysis of functional diversity was conducted, indicating ecosystems dominated by generalist species feeding upon a wide range of organisms, from plankton to marine mammals. A probabilistic approach of paleobathymetric estimation suggests a neritic environment. Previous studies based on foraminifera have suggested that the Chucunaque Formation had a greater Pacific Ocean affinity, making this the first Miocene chondrichthyan fauna described from the Pacific shelf of Panama. However, our geographic comparisons show that this fauna has mixed Caribbean and Pacific biogeographic affinities, which likely supports the previously purported connection between chondrichthyan faunas during the late Miocene.

The crustacean microcoprolite Palaxius floridanus n. isp. is described from shallow-water carbonate platform deposits of Pleistocene limestones of south Florida. Palaxius floridanus n. isp. occurs in moderate-energy packstones and grainstones of the oolite facies of the Miami Limestone, and in skeletal packstones of the Key Largo Limestone, ranging in age from marine isotope stage (MIS) 11 to MIS 5a (ca. 400–80 kyr BP). The new ichnospecies resembles P. decemlunulatus, which has been described previously from Oligocene deposits. Late Jurassic and Late Cretaceous forms described as P. decemlunulatus belong to a new ichnogenus and new ichnospecies, respectively, yet to be described.

A diverse crinoid fauna is described from the Upper Ordovician (Katian) Fombuena Formation from the eastern Iberian Chains of Spain. New crinoids include the diplobathrid camerates Fombuenacrinus nodulus n. gen. n. sp., Goyacrinus gutierrezi n. gen. n. sp., Dalicrinus hammanni n. gen. n. sp., and Ambonacrinus decorus n. gen. n. sp.; the monobathrid camerate Eopatelliocrinus hispaniensis n. sp.; and the cladid Picassocrinus villasi n. gen. n. sp. A new occurrence of Heviacrinus melendezi Gil Cid, Domínguez Alonso, and Silván Pobes, 1996 is also documented from the Castillejo Formation (Darriwilian, Middle Ordovician) from the eastern Iberian Chains of Spain. The Fombuena Formation comprises a Gondwanan crinoid assemblage from a high paleolatitude and has the highest crinoid diversity of any currently known Katian Gondwanan fauna. This assemblage is compared to other Katian age faunas around the globe, and its paleobiogeographic implications are discussed.

Lower and upper third molars of a proboscidean from the Tha Chang sand pits, Nakhon Ratchasima, northeastern Thailand, show a zygodont pattern. The crescentoids are less well developed than those of the type specimen of Zygolophodon gobiensis but similar to those of late Miocene specimens from south China assigned to Z. lufengensis and Z. chinjiensis. On the other hand, the loph(id)s are less oblique and the zygodont crests are less well developed than in Z. lufengensis and Z. chinjiensis. However, it is difficult to erect a new species for these specimens because their anterior loph(id)s are so deeply worn that the morphology of the conelets on these loph(id)s is unclear. Thus, we identify the specimens as Zygolophodon sp. Zygolophodon is known from lower and middle Miocene sediments in Africa while they are usually dated to the early–late Miocene in Europe, South Asia such as Pakistan, and Central and North China. Based on its apparent grade of dental evolution, the new material of Zygolophodon from Thailand is probably late Miocene in age. In addition, this discovery is the first record of a zygodont proboscidean in Southeast Asia.

The Meade Basin, SW Kansas, yields a rich vertebrate fossil record from the late Cenozoic. Here, we review fossil ground squirrels (Sciuridae) from the region as a contribution to the broader Meade Basin Rodent Project. We recognize 14 species in seven genera: two species of giant ground squirrels (Paenemarmota Hibbard and Schultz, 1948) from the early Pliocene, and at least 12 species in six extant genera (Ammospermophilus Merriam, 1892; Otospermophilus Brandt, 1844; Ictidomys Allen, 1877; Poliocitellus Howell, 1938; Urocitellus Obolenskij, 1927; Cynomys Rafinesque, 1817) from the Pliocene–Pleistocene sequence, including the first regional records of Ammospermophilus. Based on dental morphology and the ecology of modern congeners, we interpret faunal change through the sequence as primarily reflecting a shift from a Pliocene assemblage of “southwestern” taxa with granivorous/omnivorous diets (relatively low-crowned, transversely narrow cheek teeth) in warm and at least occasionally dry shrub or shrub-steppe habitats (Ammospermophilus, Otospermophilus, Ictidomys meadensis [Hibbard, 1941a]), to a Pleistocene temperate assemblage of grazing taxa that either exhibited relatively high-crowned, transversely wider cheek teeth (Urocitellus, Cynomys, Ictidomys tridecemlineatus [Mitchill, 1821]) or were otherwise dependent on grassland habitats (Poliocitellus). The early Pleistocene Borchers assemblage was transitional in this regard, heralding a “revolution” observed as well with other clades in the Meade Basin rodent community. This interpretation is broadly congruent with evidence of Pliocene climatic change and the staged development of regional grasslands, with the modern proportion of C3/C4 plants established in the Meade Basin during the early Pleistocene.

Waagen (1875) was the first who dealt with the Jurassic ammonites of Kutch based on detailed taxonomic work. In his monograph, he described among many species Perisphinctes spirorbis Neumayr, 1870 and P. aberrans Waagen, 1875 from the Callovian of Kutch, but the figures mentioned in the description did not correspond to the actual species. For P. spirorbis, the plate illustrated the holotype of an entirely different species (P. aberrans). On the other hand, P. spirorbis was illustrated as the lectotype of P. aberrans. Later, Spath (1924) introduced a new genus, Subgrossouvria, based on Waagen’s P. aberrans as type species. He also erected another genus, Indosphinctes, and included P. spirorbis Waagen, 1875 within the synonymy of I. indicus (Siemiradzki, 1899). Spath (1931) was aware of wrong numbering of plates of Waagen’s two species. But subsequent workers were ignorant of these taxonomic errors and continued to refer Waagen’s wrong plate numbers. We have here described both the type specimens and provided diagnoses for Spath’s two genera. We plead for this taxonomic correction in the incoming revised Treatise on Jurassic ammonites.

We report the first occurrence of an actinopterygian fish from the Lower Jurassic Navajo Sandstone, discovered in the Grand Staircase-Escalante National Monument in southern Utah, U.S.A. The site contains multiple individuals, preserved within an interdune deposit, possessing the elongate modified dorsal scales usually characterizing semionotiform fishes. The presence of moderately sized fish provides further evidence that interdune oases were occasionally persistent environmental habitats within the greater Navajo dune system, and that the paleobiota is still woefully undersampled. Additionally, this site could help fill a gap in the actinopterygian fossil record between the patchy Lower Jurassic and better-known Middle Jurassic documentation of western North America.

Moroccodiscus smithi represents a new cyclocystoid genus and species based on moldic specimens from the Middle Ordovician Taddrist Formation (Darriwilian) of SE Morocco. This represents the earliest articulated member of the Cyclocystoidea and is the first complete cyclocystoid described from the Ordovician of Gondwana, as well as the first cyclocystoid ever recorded from Africa. The anatomy and morphology of this new species were studied using a combination of conventional paleontological methods and nondestructive X-ray computed tomography. Because Moroccodiscus differs from other cyclocystoids, in particular by lacking cupules attached to the marginal ossicles, it is assigned to the new family Moroccodiscidae. This new taxon illustrates the relatively poorly known early diversification of these enigmatic extinct echinoderms and sheds light on the mode of life of cyclocystoids, including injuries to plate circlets during early ontogeny and folding of these disk-like specimens at the time of death. The overall thecal shape was very similar in cyclocystoids and many domal edrioasteroids, probably because they were both sessile or attached, benthic, suspension feeders. However, many oral surface, ambulacral, and marginal ring features had become very different, indicating that these two groups had either converged because of similar life modes or were only distantly related sister groups.

Unlike the Asian and North American Pliocene record, fossil occurrences of Canidae in Europe (and Africa) are uncommon and fragmentary. The revision of canid material from the late Pliocene site of Kvabebi (eastern Georgia) revealed the contemporaneous occurrence of three different taxa: (1) Nyctereutes megamastoides (a derived species of the Eurasian Pliocene raccoon dog-like canids); (2) Vulpes cf. V. alopecoides (representing the first occurrence of a member of the vulpine taxon V. alopecoides, a species that was the most widespread fox in the early Pleistocene in western Europe); and (3) Eucyon sp. The latter occurrence at Kvabebi completes our knowledge of the late Pliocene evolutionary history of the latest representatives of the genus in Western Europe and Central Asia. Our revision of Kvabebi canids registers a previously undocumented case of established niche partitioning among early Pliocene sympatric Canidae.

Euthycarcinoid arthropods (Cambrian–Triassic) were likely the first animals to transition from oceanic to freshwater and emergent environments. Although their basic bauplan is well known, they have a poor fossil record because their non-sclerotized exoskeleton was rarely preserved. Euthycarcinoids’ unusual morphology (varying numbers of body segments, seemingly dichotomous possession of either mandibles or a labrum, specialized or generalized limbs, and possession by some euthycarcinoid species of sternal pores—structures possibly analogous to coxal vesicles in myriapods) contribute to uncertainty regarding their relationship to other arthropod groups; while their poor fossil record masks the evolutionary transitions within and between the separate realms they inhabited (marine, freshwater, emergent). A new euthycarcinoid from a Permian polar proglacial lake is described herein that is morphologically unlike all other euthycarcinoids, and interpreted as being well adapted for a nekton-benthic lifestyle. Antarcticarcinus pagoda n. gen. n. sp. possesses a pair of large wing-like processes that project laterally from the preabdominal dorsal exoskeleton. A trace fossil from the overlying Mackellar Formation, cf. Orbiculichnus, which was previously interpreted as having been produced by insects taking off or landing on wet sediments, is reinterpreted herein as being produced by A. pagoda n. gen. n. sp. due to the high degree of morphological similarity between traces and body fossils. This occurrence indicates that euthycarcinoids were able to adapt to life in temperate freshwater environments, while possible subaerial adaptations hint at an ability to breathe air. Indeed, if euthycarcinoids could breathe air, Cambrian terrestrial forays and rapid transition (by the Ordovician) into freshwater environments might be explained.

Priacanthids are a small family of percomorph fishes comprising fewer than 20 extant species currently assigned to four genera. One of these, Pristigenys, was established by Louis Agassiz (1835) to include the Eocene species Pristigenys substriata from Monte Bolca, and is usually regarded as a subjective senior synonym of Pseudopriacanthus. Consequently, Pristigenys currently comprises five extant species plus the fossil Pristigenys substriata. The osteology of the type species of this genus, however, is poorly known, and this makes it difficult to provide an adequate comprehensive definition of the taxonomy of the whole family. Pristigenys substriata is redescribed in detail based on five well-preserved articulated skeletons. Pristigenys substriata can be easily distinguished from other priacanthids based on its unique combination of characters. Morphological analysis of the fossil specimens reveals that there is substantial evidence to justify recognition of both Pristigenys and Pseudopriacanthus as valid genera, with extant species previously assigned to Pristigenys now referred to Pseudopriacanthus. Within the Priacanthidae, Pristigenys and Pseudopriacanthus form sister taxa and this pair can be considered as the sister-group to all remaining extant priacanthid genera (Cookeolus + [Heteropriacanthus+Priacanthus]).

The Archaeopithecidae is a very poorly known group of native ungulates from the Eocene of Patagonia (Argentina), whose alpha taxonomy has remained obscure since Ameghino’s times. It is traditionally considered as a family representative of the Casamayoran (middle Eocene) South American Land Mammal Age, and is thought to be morphologically close to the notopithecids. After studying >200 specimens from several institutions, including all the type specimens, a taxonomic overestimation is established. Out of the six species considered originally as archaeopithecids, Archaeopithecus rogeri Ameghino, 1897 is here recognized as the only valid name and species; subsequent synonymies are proposed and previous taxonomic hypotheses discarded. This exhaustive revision has permitted improving the knowledge of A. rogeri and, for the first time, it has revealed many craniodental characters, which allow amending its diagnosis and differentiating this taxon from other Eocene notoungulates. Archaeopithecus rogeri is a small-sized taxon characterized by its complete and rooted dentition, which is relatively higher than that of other contemporaneous short-crowned notoungulates and shows ontogenetic variation in size and morphology. The body mass range of A. rogeri (1.4–2.5 kg) is comparable to those of notopithecids and some small hegetotheriids. The phylogenetic analysis shows A. rogeri is not directly related to any family within Notoungulata, appearing into a polytomy, as a basal taxon of typotherians. The biochronological range of A. rogeri is adjusted to Vacan (middle Eocene) through Barrancan subages (late middle Eocene); older (Riochican, late early Eocene) and younger (Mustersan, late Eocene) records remain to be confirmed.

The Holocystites Fauna is an enigmatic group of North American diploporitans that presents a rare window into unusual middle Silurian echinoderm communities. Multiple systematic revisions have subdivided holocystitids on the basis of presumed differences in oral area plating and respiratory structures. However, these differences were based on a fundamental misunderstanding of the homologous elements of the oral area and the taphonomic process; taphonomic disarticulation of the oral area formed the basis for the erection of Pentacystis and Osgoodicystis as separate genera, and Osgoodicystis is interpreted as the junior synonym of Pentacystis. Holocystitids show a conservative peristomial bordering plate pattern that is shared among all described genera. The peristome is bordered by seven interradially positioned oral plates as is typical for oral plate–bearing blastozoans. A second open circlet of facetal plates lies distal to the oral plates; five of these facetal plates bear facets for feeding appendages (lost on the A ambulacrum in some taxa), while two lateral facets (present in all taxa except Pustulocystis) do not. Holocystitid taxa show minor modifications to this basic peristomial bordering plate pattern. As thecal morphologies are highly variable within populations, taxonomic revision of holocystitids is based on modifications of the plating of the oral area.

The Sinoalidae, as one of the three Mesozoic froghopper families, was recently recognized from the latest Middle–earliest Late Jurassic Daohugou Biota of northeastern China. We herein report some new materials from the same horizon and locality, providing some new insights on morphological diversity and evolution of this family. Shufania hani new genus new species indicates that the relative branching position of veins M and CuA of the forewing is highly variable within the Sinoalidae and not appropriate for family-level diagnosis. The venations of three reported sinoalid hind wings are conservative, likely due to its simplified topology and reduced terminal branches. Color patterns of hind wings are likely variable for different sinoalid froghoppers. However, considering that color pattern is easily weakened or even erased by diagenetic processes for imprint fossils, the morphological character is not reliable for distinguishing different sinoalid taxa. Additionally, our new material suggests that the number of lateral spines of the hind tibia can vary intra-individually for sinoalids, just as in some recent froghoppers.

The Permian is regarded as one of the most crucial intervals during echinoid evolution because crown group echinoids are first widely known from the Permian. New faunas provide important information regarding the diversity of echinoids during this significant interval as well as the morphological characterization of the earliest crown group and latest stem group echinoids. A new fauna from the Capitanian Lamar Member of the Bell Canyon Formation in the Guadalupe Mountains of West Texas comprises at least three new taxa, including Eotiaris guadalupensis Thompson n. sp. an indeterminate archaeocidarid, and Pronechinus? sp. All specimens represented are silicified and known from disarticulated or semiarticulated interambulacral and ambulacral plates and spines. This assemblage is one of the most diverse echinoid assemblages known from the Permian and, as such, informs the paleoecological setting in which the earliest crown group echinoids lived. This new fauna indicates that crown group echinoids occupied the same environments as stem group echinoids of the Archaeocidaridae and Proterocidaridae. Furthermore, the echinoids described herein begin to elucidate the order of character transitions that likely took place between stem group and crown group echinoids. At least one of the morphological innovations once thought to be characteristic of early crown group echinoids, crenulate tubercles, was in fact widespread in a number of stem group taxa from the Permian as well. Crenulate tubercles are reported from two taxa, and putative cidaroid style U-shaped teeth are present in the fauna. The presence of crenulate tubercles in the archaeocidarid indicates that crenulate tubercles were present in stem group echinoids, and thus the evolution of this character likely preceded the evolution of many of the synapomorphies that define the echinoid crown group.

Twenty-one species of echinoid are reported from Paleocene rocks of the eastern United States along the outcrop belt from Texas to New Jersey. Six of these are strictly early Paleocene age (Danian), nine strictly late Paleocene age (Thanetian), five range throughout the Paleocene, and one previously reported Paleocene species (Diplodetus moscovensis) is most likely a Cretaceous species. Two new species are described, Salenia palmyra n. sp., from the Danian Clayton Formation in Alabama and Georgia, and Ova rancoca n. sp., from the Thanetian Vincentown Formation in New Jersey. One new species from the Clayton Formation in Mississippi, Arbaciella? sp., is left in open nomenclature.

A new species of toxodontid notoungulate, Xotodon maimarensis n. sp., is described from the Maimará Formation (late Miocene–early Pliocene), Jujuy Province, northwestern Argentina. This is the first record of a toxodontid from the Eastern Cordillera. The specimen is housed at the Museo de Geología, Mineralogía y Paleontología, Instituto de Geología y Minería de la Universidad Nacional de Jujuy. It consists of an incomplete mandible preserving the right mandibular ramus with part of the dental series, partially preserved symphysis with all the incisors, and a small portion of the left ramus without teeth. The following characters distinguish it as a new taxon: symphysis long and narrow with slight divergence of its lateral borders; strong procumbence of lower incisors and deeply implanted i3; chin angle lower than in X. major and X. cristatus and bulging labial keel limiting strong lateral concavities. Comparative analysis in the context of the recently revised Neogene Toxodontidae indicates that the Maimará specimen shares mandibular features and dental characters with Xotodon and Mixotoxodon, differing from the latter by the more upraised symphysis. The phylogenetic position of Xotodon maimarensis n. sp. supports the taxonomic interpretation of the studied specimen as a new species of Xotodon. This new Toxodontidae increases the knowledge of the diversity and radiation of this group of notoungulates in northwest Argentina.

Two middle Permian (Capitanian) to Early Triassic (Griesbachian) rugosochonetidae brachiopod genera, Fusichonetes Liao in Zhao et al., 1981 and Tethyochonetes Chen et al., 2000, have been regarded as two distinct taxa and used as such for a wide range of discussions including biostratigraphy, paleoecology, paleobiogeography, and the Permian-Triassic boundary mass extinction. However, the supposed morphological distinctions between the two taxa are subtle at best and appear to represent two end members of a continuum of morphological variations. In this study, we applied a range of quantitative and analytical procedures (bivariate plots, Kolmogorov-Smirnov test, categorical principle component analysis, and cladistic analysis) to a dataset of 15 quantified morphological variables, integrating both key external and internal characters, measured from 141 specimens of all well-known Fusichonetes and Tethyochonetes in order to test whether or not these two genera could be distinguished in view of the chosen characters. The results indicate that these two genera are morphologically indistinguishable and that the species classification previously applied to these two genera appears to represent polyphyletic groupings within the genus Fusichonetes. Consequently, Tethyochonetes is concluded to be a junior synonym of Fusichonetes. The diagnosis and key characteristics of Fusichonetes are clarified and refined based on a new suite of well-preserved specimens from the Permian−Triassic Xinmin section in South China.