Stratigraphy of the Haut Var Paleogene continental series (Northeastern Provence, France): New insight on the age of the 'Sables bleutés du Haut Var' Formation

The age of the Paleogene deposits of the Haut Var (Provence, France) has been the subject of debate. Particularly, the ''Calcaire à Bithynies'' and the ''Sables bleutés'' units were ascribed either to the early Eocene or to the Oligocene. A stratigraphical clarification is required in order to precise the paleogeographical relationships of the Haut Var Paleogene sedimentary series with coeval deposits in the neighbouring southern Provence and Subalpine regions and other European domains. The study area is characterized by tectonically separated synclines and grabens filled in by continental Paleogene deposits. Detailed mapping and lithostratigraphical logging, sedimentological and microfacies analysis have been undertaken in order to provide a reliable stratigraphical framework. Biostratigraphical subdivisions were established based on five different fossil groups: mammals, charophytes, gastropods, ostracodes, and foraminifers. Accordingly, five formations are distinguished and dated: ''Calcaire a` Microcodium'' and ''Brèche à Microcodium'' (Danian); ''Marnes à oeufs d'oiseaux'' (Selandian(?)-earliest Ypresian); 'Sables bleutés du Haut Var' (early-late(?) Ypresian); and ''Bourdas conglomerates'' (Rupelian). Particular emphasis is given to the study of the controversial 'Sables bleute´ s du Haut Var' Formation. As a result, correlations have been established between the different syncline and graben areas where Paleocene-Eocene and Oligocene deposits occur. Terrestrial deposits (carbonate paleosols and piedmont alluvial fans) took place during Paleocene times, while fluvial (cross-bedded sands) and lacustrine carbonate deposits developed in a foreland compressional intracontinental basin surrounded by emerged areas and tectonic highs during the early Ypresian. Paleoenvironmental and paleogeo- graphical analysis strengthen the view that a relative isolation characterized the Haut Var area during the early Eocene, probably enhancing episodes of brackish water or evaporitic sedimentation and gastropod endemism. During the late Eocene Pyrenean-Provence tectonic phase, the E-W trending Haut Var overthrusts have been emplaced posteriorly to the deposition of the 'Sables bleute´ s du Haut Var' Fm. Finally, coarse alluvial fan and local lacustrine carbonate sedimentation occurred during the Oligocene in narrow N-S trending subsident extensional grabens associated with the N-S trending Barjols Triassic uplift

Dental eruption and growth in Hyracoidea (Mammalia, Afrotheria)

We investigated dental homologies, development, and growth in living and fossil hyracoids, and tested if hyracoids and other mammals show correlations between eruption patterns, gestation time, and age at maturity. Unlike living species, fossil hyracoids simultaneously possess replaced P1 and canine teeth. Fossil species also have shorter crowns, an upper and lower I3 locus, an upper I2, and a hypoconulid on m3. Prenatal specimens of the living $\textit{Procavia capensis}$ and $\textit{Heterohyrax brucei}$ show up to three tooth buds posterior to upper dI1 and anterior to the seven upper cheek teeth that consistently erupt; these include an anterior premolar but not a canine. Most lower cheek teeth finish eruption during growth in hyracoids, not after growth as in most other afrotherians. All hyracoids show the m1 at (lower) or near (upper) the beginning of eruption of permanent teeth; M3/m3 is the last permanent tooth to erupt. The living P. capensis erupts most lower antemolar loci before m2. In contrast, fossil hyraxes erupt lower antemolars after m2. While the early eruption of antemolars correlates with increased gestation time and age at maturity in primates and $\textit{Tupaia}$ (i.e., "Schultz's Rule"), and while modern hyraxes resemble some anthropoid primates in exhibiting long gestation and eruption of antemolars at or before molars, eruption patterns do not significantly co-vary with either life history parameter among afrotherians sampled so far. However, we do observe a shift in eruption timing and crown height in $\textit{Procavia}$ relative to fossil hyracoids, mirroring observations recently made for other ungulate-grade mammals.Collection of Fayum hyracoids has been funded by U.S. National Science Foundation grants to E. L. Simons (BCS-0114856), to ELS and E. R. Seiffert (BCS- 0416164), to ERS (BCS-0819186), and to ERS, J. G. Fleagle, G. F. Gunnell, and D. M. Boyer (BCS-1231288). Fieldwork was undertaken in collaboration with the Egyptian Mineral Resources Authority and the Egyptian Geological Museum, and was managed by P. Chatrath. RJA, LH, and DP acknowledge support from the Leverhulme Trust and the Department of Zoology, University of Cambridge. We thank C. Riddle and V. Yarborough for access to fossils and fossil preparation, and C. Soubiran for help with segmentation of extant hyrax CT scans. Some CTscan data presented in this work were produced thanks to the imaging facilities of the MRI Platform and of the LabEx CeMEB (Montpellier)

Evidence for a Grooming Claw in a North American Adapiform Primate: Implications for Anthropoid Origins

Among fossil primates, the Eocene adapiforms have been suggested as the closest relatives of living anthropoids (monkeys, apes, and humans). Central to this argument is the form of the second pedal digit. Extant strepsirrhines and tarsiers possess a grooming claw on this digit, while most anthropoids have a nail. While controversial, the possible presence of a nail in certain European adapiforms has been considered evidence for anthropoid affinities. Skeletons preserved well enough to test this idea have been lacking for North American adapiforms. Here, we document and quantitatively analyze, for the first time, a dentally associated skeleton of Notharctus tenebrosus from the early Eocene of Wyoming that preserves the complete bones of digit II in semi-articulation. Utilizing twelve shape variables, we compare the distal phalanges of Notharctus tenebrosus to those of extant primates that bear nails (n = 21), tegulae (n = 4), and grooming claws (n = 10), and those of non-primates that bear claws (n = 7). Quantitative analyses demonstrate that Notharctus tenebrosus possessed a grooming claw with a surprisingly well-developed apical tuft on its second pedal digit. The presence of a wide apical tuft on the pedal digit II of Notharctus tenebrosus may reflect intermediate morphology between a typical grooming claw and a nail, which is consistent with the recent hypothesis that loss of a grooming claw occurred in a clade containing adapiforms (e.g. Darwinius masillae) and anthropoids. However, a cladistic analysis including newly documented morphologies and thorough representation of characters acknowledged to have states constituting strepsirrhine, haplorhine, and anthropoid synapomorphies groups Notharctus tenebrosus and Darwinius masillae with extant strepsirrhines rather than haplorhines suggesting that the form of pedal digit II reflects substantial homoplasy during the course of early primate evolution

Vicariance and dispersal in southern hemisphere freshwater fish clades: a palaeontological perspective

Widespread fish clades that occur mainly or exclusively in fresh water represent a key target of biogeographical investigation due to limited potential for crossing marine barriers. Timescales for the origin and diversification of these groups are crucial tests of vicariant scenarios in which continental break‐ups shaped modern geographic distributions. Evolutionary chronologies are commonly estimated through node‐based palaeontological calibration of molecular phylogenies, but this approach ignores most of the temporal information encoded in the known fossil record of a given taxon. Here, we review the fossil record of freshwater fish clades with a distribution encompassing disjunct landmasses in the southern hemisphere. Palaeontologically derived temporal and geographic data were used to infer the plausible biogeographic processes that shaped the distribution of these clades. For seven extant clades with a relatively well‐known fossil record, we used the stratigraphic distribution of their fossils to estimate confidence intervals on their times of origin. To do this, we employed a Bayesian framework that considers non‐uniform preservation potential of freshwater fish fossils through time, as well as uncertainty in the absolute age of fossil horizons. We provide the following estimates for the origin times of these clades: Lepidosireniformes [125–95 million years ago (Ma)]; total‐group Osteoglossomorpha (207–167 Ma); Characiformes (120–95 Ma; a younger estimate of 97–75 Ma when controversial Cenomanian fossils are excluded); Galaxiidae (235–21 Ma); Cyprinodontiformes (80–67 Ma); Channidae (79–43 Ma); Percichthyidae (127–69 Ma). These dates are mostly congruent with published molecular timetree estimates, despite the use of semi‐independent data. Our reassessment of the biogeographic history of southern hemisphere freshwater fishes shows that long‐distance dispersals and regional extinctions can confound and erode pre‐existing vicariance‐driven patterns. It is probable that disjunct distributions in many extant groups result from complex biogeographic processes that took place during the Late Cretaceous and Cenozoic. Although long‐distance dispersals likely shaped the distributions of several freshwater fish clades, their exact mechanisms and their impact on broader macroevolutionary and ecological dynamics are still unclear and require further investigation.Peer Reviewedhttps://deepblue.lib.umich.edu/bitstream/2027.42/148368/1/brv12473_am.pdfhttps://deepblue.lib.umich.edu/bitstream/2027.42/148368/2/brv12473.pd

A eutherian mammal in the latest Cretaceous of Vitrolles, Southern France

In Europe, the fossil record of the eutherian mammals is very scanty for the Late Cretaceous, as only two genera, documented by isolated teeth, are presently recorded in France and in Spain. Both genera, Labes and Lainodon, are considered to be representatives of the “zhelestids”, a paraphyletic unit regarded as being at the origin of Cenozoic ungulates within the Ungulatomorpha clade. We here describe Valentinella vitrollense gen. et sp. nov. from Vitrolles la Plaine (Maastrichtian, southern France). This species, represented by fragmentary remains of lower and upper dentitions, is tentatively assigned to the “zhelestids” according to the hypoconulid−entoconid twinning and the antero−posteriorly short trigonid on m1–3. The occlusal surfaces are obliterated by dental attrition, but Valentinella could be an evolved “zhelestid”, more derived than Labes and Lainodon by its fully compressed trigonid. Valentinella is similar to Gallolestes by other derived characters such as a crushing specialization of the teeth, associated with a probably molariform p4 (or dp4) and slightly reduced m3. The enamel microstructure, showing a radial prismatic pattern combined with a reduced interprismatic matrix, in which cristallites are oriented at about 45° to the prisms axes, appears compatible with the ancestral morphotype for all ungulates; although no synapomorphy can be proposed for the ungulatomorphs

Revised age estimates for the later Paleogene mammal faunas of Egypt and Oman

The Jebel Qatrani Formation of northern Egypt has produced Afro-Arabia’s primary record of Paleogene mammalian evolution, including the world’s most complete remains of early anthropoid primates. Recent studies of Fayum mammals have assumed that the Jebel Qatrani Formation contains a significant Eocene component (≈150 of 340 m), and that most taxa from that succession are between 35.4 and 33.3 million years old (Ma), i.e., latest Eocene to earliest Oligocene in age. Reanalysis of the chronological evidence shared by later Paleogene strata exposed in Egypt and Oman (Taqah and Thaytiniti areas, Dhofar Province) reveals that this hypothesis is no longer tenable. Revised correlation of the Fayum and Dhofar magnetostratigraphies indicates that (i) only the lowest 48 m of the Jebel Qatrani Formation are likely to be Eocene in age; (ii) the youngest Fayum anthropoids, including well known species such as Aegyptopithecus zeuxis and Apidium phiomense, are probably between 30.2 and 29.5 Ma, ≈3–4 Ma younger than previously thought; (iii) oligopithecid anthropoids did not go extinct at the Eocene–Oligocene boundary but rather persisted for at least another 2.5 Ma; (iv) propliopithecid anthropoids first appear in the Fayum area at ≈31.5 Ma, long after the Eocene–Oligocene boundary; and (v) the youngest Fayum mammals may be only ≈1 Ma older than the 28- to 27-Ma mammals from Chilga, Ethiopia, and not 4–5 Ma older, as previously thought. Whatever gap exists in the Oligocene record of Afro-Arabian mammal evolution is now limited primarily to a poorly sampled 27- to 23-Ma window in the latest Oligocene