A new plesiadapiform primate, Phoxomylus puncticuspis gen. et sp. nov., is described based on an isolated but well-preserved upper molar from the early Tiffanian (late Paleocene) Cochrane 2 locality, southwestern Alberta, Canada. Although possessing a robust postprotoconal fold, an unambiguous synapomorphy of primates, Phoxomylus differs from other plesiadapiforms in its retention of primitive molar features, including acutely pointed major cusps and sharp crests, deep trigon basin, and lack of the bunodont coronal specializations that purportedly marked the transition from insectivorous non-primate ancestors to omnivorous/frugivorous basal primates. Coronal features of the holotype of P. puncticuspis imply that during mastication the mandible was adducted in a near-vertical plane, with little capacity for the transverse movement that is already seen in molar morphology of the earliest and most basal plesiadapiform, Purgatorius. Instead, molar morphology in P. puncticuspis implies emphasis on vertical piercing and shearing, specializations for insectivory unlikely to have been derived via reversal from plesiadapiform ancestors having more bunodont molars adapted for omnivory/frugivory. If that is the case, a long “ghost lineage” must link P. puncticuspis to other, basal plesiadapiforms that have yet to be discovered but that had not yet evolved omnivorous adaptations of the dentition.

Four different Hunter-Schreger Band (HSB) configurations were observed in the teeth of fossil and extant Perissodactyla. This variability exceeds that observed in Artiodactyla or Proboscidea. The four HSB configurations represent two different evolutionary pathways. Transverse HSB found in many mammalian taxa outside the Perissodactyla represents the most primitive HSB configuration. It occurs in several primitive perissodactyl families and is retained in Palaeotheriidae and extant Equidae. Curved HSB evolved from transverse HSB and occurs in Tapiridae, Helaletidae, and Lophiodontidae, as well as in Ancylopoda and Titanotheriomorpha. This likely indicates independent evolution of curved HSB in two or more lineages, but the number of instances of parallelism of this configuration is obscured by uncertainty in the relationships among these taxa and by a lack of data for some important basal taxa. A second evolutionary pathway leads from transverse HSB via compound HSB to vertical HSB. Compound HSB were detected in Hyrachyidae, Deperetellidae, and the early rhinocerotid Uintaceras. Vertical HSB configuration characterizes the molar dentition of other Rhinocerotidae, Hyracodontidae, Indricotheriidae, and Amynodontidae. Often, the incisors of rhinocerotids retain traces of compound HSB. Thus the HSB configuration reflects phylogenetic relationships to some degree. The selective value of the modified HSB configurations is interpreted functionally as a mechanism to reduce abrasion during mastication, assuming that the perpendicular intersection of prisms with the actual grinding surfaces resists wear better than prisms running parallel to the occlusal surface.

Communities of large mammals exhibit changes in morphological diversity through space and time; changes that are possibly correlated to distinct aspects of the physical environment. Here, I explore shape changes in the trophic apparatus of large carnivore guilds, comparing extant communities with Quaternary ones, from peninsular Italy. Mandibular shape is quantified through geometric morphometrics and its disparity is computed for each carnivore guild. Patterns of morphospace occupation through space and time reveal that extant carnivore guilds are negatively influenced by number of artiodactyls. Very productive ecosystems show low values of morphological disparity because species tend to occupy central regions of the morphospace rather than extreme areas. Disparity of mandibular corpus shape remains relatively stable throughout the Quaternary in the large carnivore communities of the Italian peninsula. They exhibit similar values to extant guilds because the trophic apparatus did not evolved important morphological novelties. Interestingly, carnivore guilds of the late Pliocene (3.5 Ma) and early Pleistocene (0.8 Ma) show over-dispersed or random morphospace occupation because of a depleted fauna, precluding successive structural changes. The same applies for the extant European carnivore guild as a result of recent extinctions without replacement.

Knowledge of titanosaurian cranial anatomy has improved substantially in the last decade because several skulls have come to light or were restudied. The discovery of Bonitasaura salgadoi, a partial titanosaurian skeleton including cranial bones, permitted the definitive recognition of square jaws in a titanosaurian sauropod as well as a peculiar skull morphology that increases the morphological diversity of the group. Here we present a full description and illustration of the skull material of B. salgadoi. Among cranial bones, the lacrimal, quadrate, and dentary exhibit apomorphic differences from those of other titanosaurians. Conversely, the frontal and parietal are more conservative. A phylogenetic analysis recovers B. salgadoi as a member of the Titanosauria, related to mid-sized to large titanosauroids from the Turonian—Campanian of South America, in contrast to a previous hypothesis that suggested a nemegtosaurid affinity. The skull reconstruction presented here shows that the skull of B. salgadoi is anteroposteriorly short and dorsoventrally high, contrasting with the elongate skull of Rapetosaurus krausei.

The Late Cretaceous South American sauropods Neuquensaurus australis and Saltasaurus loricatus are represented by well-preserved and abundant material that has been integral to our understanding of titanosaur anatomy for decades. Although the hypodigms for these species span most of the skeleton, holotypic materials are limited to a few bones that do not overlap between the two taxa. In this contribution, we augment the holotype of Neuquensaurus australis with a partial sacrum that was preserved in articulation with one of the caudal vertebrae from its original description, but not recognised as such at the time. We document this field association via the presence of a broken piece of matrix on the sixth sacral vertebral centrum that has a snap-fit to matrix on the rim of the anterior condyle of the holotypic biconvex vertebra. Based on comparisons with a more complete sacrum and ilium of a referred specimen of Neuquensaurus australis, we interpret this biconvex vertebra to be the seventh sacral vertebra. This raises the possibility that the biconvex “first caudal” vertebra of some other titanosaurs may be part of the sacrum as well. Augmentation of the Neuquensaurus australis holotype to include a sacrum makes it directly comparable to the holotype of Saltasaurus loricatus. Morphological differences in the number, shape, and proportion of sacral vertebrae allow discrimination between Neuquensaurus and Saltasaurus, confirming their generic separation. The El Brete quarry, which preserves the holotypic sacrum and abundant referred specimens of Saltasaurus loricatus, also preserves a sacrum consisting of seven vertebrae that bears autapomorphies of Neuquensaurus australis, indicating that these two saltasaurines coexisted.

Brontomerus mcintoshi is a new genus and species of sauropod dinosaur from the Hotel Mesa Quarry in Grand County, Utah, USA, in the upper part of the Ruby Ranch Member (Aptian—Albian) of the Lower Cretaceous Cedar Mountain Formation. It is known from at least two fragmentary specimens of different sizes. The type specimen is OMNH 66430, the left ilium of a juvenile individual; tentatively referred specimens include a crushed presacral centrum, a complete and well-preserved mid-to-posterior caudal vertebra, the partial centrum of a distal caudal vertebra, a complete pneumatic anterior dorsal rib from the right side, the nearly complete left scapula of a much larger, presumably adult, individual, and two partial sternal plates. Brontomerus is diagnosed by five autapomorphies of the type specimen: preacetabular lobe 55% of total ilium length, longer than in any other sauropod; preacetabular lobe directed anterolaterally at 30° to the sagittal, but straight in dorsal view and vertically oriented; postacetabular lobe reduced to near absence; ischiadic peduncle reduced to very low bulge; ilium proportionally taller than in any other sauropod, 52% as high as long. In a phylogenetic analysis, Brontomerus was recovered as a camarasauromorph in all most parsimonious trees, but with uncertain position within that clade. The large preacetabular lobe of the ilium anchored powerful protractor and abductor muscles, but precise interpretation is impossible without functionally related elements such as femora and proximal caudal vertebrae. Brontomerus is the eighth sauropod genus named from the Early Cretaceous of North America, and more remain to be described: North American sauropod diversity did not decline catastrophically at the end of the Jurassic as often assumed. The most striking differences between Late Jurassic and Early Cretaceous sauropod faunas in North America is that the former are abundant and dominated by diplodocids, whereas the latter are comparatively scarce— though still diverse—and dominated by macronarians.

The shape and extent of the membranous brachioptagium in pterosaurs remains a controversial topic for those attempting to determine the aerodynamic performance of the first vertebrate fliers. Various arguments in favour of the trailing edge terminating against either the torso or hip, the femur, the ankle, or different locations for various taxa, has resulted in several published reconstructions. Uncertainty over the correct model is detrimental to both aerodynamic and palaeoecological studies that are forced to simultaneously consider multiple and highly variable configurations for individual taxa. A review of relevant pterosaur specimens with preserved soft tissues or impressions of the wing membrane, however, strongly suggests that the trailing edge of the wing extended down to the lower leg or ankle in all specimens where the brachiopatagium is completely preserved. This configuration is seen across a phylogenetically broad range of pterosaurs and is thus likely to have been universally present throughout the Pterosauria. Support for opposing hypotheses where the trailing edge terminates against the body, hip, or knee are based on several specimens where the wing membrane is either incomplete or has undergone post-mortem contraction. An ankle attachment does not rule out a high aspect ratio wing as the curvature of the trailing edge and the ratio of the fore to hind limbs also play a major role in determining the final shape of the membrane.

A new basal sphenacodontid synapsid, represented by an anterior portion of a mandible, demonstrates for the first time the presence of amniotes in the largest European Permo-Carboniferous basin, the Saar-Nahe Basin. The new taxon, Cryptovenator hirschbergeri gen. et sp. nov., is autapomorphic in the extreme shortness and robustness of the lower jaw, with moderate heterodonty, including the absence of a greatly reduced first tooth and only a slight caniniform development of the second and third teeth. Cryptovenator shares with Dimetrodon, Sphenacodon, and Ctenospondylus, but notably not with Secodontosaurus, enlarged canines and a characteristic teardrop outline of the marginal teeth in lateral view, possession of a deep symphyseal region, and a strongly concave dorsal margin of the dentary. The new find shows that sphenacodontids were present in the Saar-Nahe Basin by the latest Carboniferous, predating the record of sphenacodontid tracks from slightly younger sediments in this region.

A rich conodont fauna from two Neotethyan sections, Pizzo Mondello (western Sicily, Italy) and Pignola 2 sections (southern Apennines, Italy) includes conodonts described herein as a new species. Metapolygnathus praecommunisti sp. nov. is transitional between Paragondolella noah and Metapolygnathus communisti. The genus Metapolygnathus (including M. praecommunisti) is now characterised by posterior prolongation of the keel termination, associated with a centrally located pit and with a weak ornamentation confined to the anterior part of the platform margins. The establishment of M. praecommunisti addresses the problems related to the origin and the peculiar, probably facies-controlled, distribution of its descendant species M. communisti. Since M. praecommunisti occurs in the entire Tethys and in North America, we propose the species as a good guide fossil for global correlations, characterised by a short temporal range limited to the uppermost Tuvalian (upper Carnian). The stratigraphic occurrence of the genus Metapolygnathus is restricted to the Tuvalian—Lacian (upper Carnian—lower Norian), excluding its presence in the Julian substage (lower Carnian).

The precise record of simoceratins sampled bed-by-bed is first reported from Mexico (Mazatepec area in Puebla, central-eastern Mexico), as well as the existence of lappeted peristomes in these ammonites. Both Pseudovolanoceras aesinense and the subspecies Pseudovolanoceras aesinense chignahuapense are shown to occur among Mexican simoceratins. The European species and the Mexican subspecies share the same stratigraphic range in the studied sections, yet they differ in ephebic sculpture. Ecological adaptation to neritic seas corresponding to eastern Mexico areas is interpreted, forcing phenotypic deviation with geographic significance, i.e., subspeciation. The new subspecies would indicate stratigraphic horizons within the Semiformiceras semiforme/Haploceras verruciferum Chronozone in the Mediterranean Tethys. A revision of contemporaneous simoceratins in the Americas is founded on a comparative analysis with respect to the European species P. aesinense.

Raised shell projections on the inner shell walls that form pits on the internal moulds of Devonian ammonoids have been known for several decades. New specimens from Morocco reveal novel details of these structures; most, if not all, of which consist of a capsule of ammonoid shell that covers tiny tubes attached to the outer (= lateral or ventral) shell wall from the inside. In accordance with comparable Recent occurrences of similar structures in molluscs, we use the term “pearls” for these structures and the pits they form on the internal moulds. The nature of these encapsulated tubes is described and discussed. Because of the presence of these tubes inside the pearls, pearl arrangement, and their similarity to Recent mollusc occurrences, the tubes are interpreted as traces of parasitoses. The pearls and pits were grouped into five types based on differences in morphology, size, and arrangement. Then, having used these traits to perform a simple cladistic analysis, the resulting cladogram was compared to the phylogeny of ammonoids. Based on this comparison, it appears likely that the parasites underwent a co-evolution with the ammonoids, which lasted 10 to 15 Ma. Patterns of evolutionary events include co-speciation, “drowning on arrival” (end of parasite lineage near base of a new host clade), and “missing the boat” (parasite lineage does not adapt to a new host clade, thus not evolving a new parasite clade). Because of the lack of fossilised soft tissue, only speculations can be made about the systematic affiliation of the parasites, their life-cycle, infection strategy, and ecological framework. Some co-occurring bivalves also have pits reminiscent to structures caused by trematodes in Recent forms. Based on the available information, the tubes are interpreted as artefacts of trematode infestations, which, if correct, would extend the fossil record of parasitic trematodes into the Early Devonian.

The types of the species belonging to the fusulinid genera Schubertella and Eoschubertella were examined from publications and type collections. Eoschubertella in general possesses all the features of Schubertella and therefore is a junior synonym of the latter. However, the concept of Eoschubertella best describes the genus Schubertina with its type species Schubertina curculi. Schubertina is closely related to the newly established genus Grovesella the concept of which is emended in this paper. Besides Schubertella, Schubertina, and Grovesella, the genera Mesoschubertella, Biwaella are reviewed and three new species, Grovesella nevadensis, Biwaella zhikalyaki, and Biwaella poletaevi, are described. The phylogenetic relationships of all Pennsylvanian—Cisuralian schubertellids are also proposed. Barrel-shaped Grovesella suggested being the very first schubertellid that appears sometimes in the middle—late Bashkirian time. In late Bashkirian it is then developed into ovoid to fusiform Schubertina. The latter genus gave rise into Schubertella in early Moscovian. First Fusiella derived from Schubertella in late Moscovian, Biwaella—in early Gzhelian and Boultonia—in late Gzhelian time. Genus Mesoschubertella also developed from Schubertella at least in Artinskian, but may be in late Sakmarian.

Triassic microfloras from Antarctica contain abundant lycophyte spores. However, macrofossils of this group of plants are missing, and thus the precise affinities of the spore producers remain unknown. Macrofossil remains of a pleuromeialean lycophyte, including an incomplete strobilus, isolated sporophylls and sporangia, as well as abundant megaspores, occur on a single rock sample from the central Transantarctic Mountains. Also occurring on the same surface is Mesenteriophyllum serratum, a strap-shaped leaf morphotype of uncertain affinity previously known only from the Kyrgyz Republic and the Taimyr Peninsula. The leaves display alternating transverse ridges and depressions that are similar to structures seen in compressed leaves of various isoetalean lycophytes. Leaf morphology and anatomy, together with the close association of the other lycophyte remains, suggest that M. serratum represents a pleuromeialean lycophyte leaf, which was part of the same plant that produced the sporophylls and sporangia. Sedimentological data indicate that this lycophyte inhabited a swampy, probably coal-forming overbank environment, which contrasts with the assumed xero- to halophytic habit of many other pleuromeialean lycophytes.

In the light of integrated biostratigraphic and geochemical data, a complete shallow-marine succession across the Cretaceous—Palaeogene (K—Pg) boundary, with the critical boundary clay coupled with a burrowed siliceous chalk (“opoka” in Polish geological literature), possibly equivalent of the basal Danian Cerithium Limestone in Denmark, has been discovered at Lechówka near Chelm, SE Poland. An extraterrestrial signature marking the K—Pg boundary is confirmed by anomalously high amounts of iridium (up to 9.8 ppb) and other siderophile elements (especially Au and Ni), as well as by an elevated Ir/Au ratio consistent with a chondrite meteoritic composition. The major positive iridium spike surprisingly occurs in Maastrichtian marls, 10 cm below the boundary clay interval, which can be explained by diagenetic mobilisation and re-concentration of the impact-derived components. Thus, intensively infiltrating, humic acid-rich ground waters during the long-lasting Palaeogene weathering in tropical humid regimes were probably responsible not only for the large-scale decalcification of the Lechówka section, but also for both downward displaced position of the iridium enrichment, a dispersed profile of this anomaly and its significantly lessened value, but still approaching an increase by a factor of 100. This modified record of the K—Pg boundary event points to a careful reconsideration of the iridium anomaly as a trustworthy marker for studying the extinction patterns across the K—Pg boundary, as supported by the recent data from New Jersey, USA.