A partial skull of Ardynomys russelli sp. nov. (Rodentia, Cylindrodontidae) is described. This was collected in the late Eocene of Alag Tsab locality in the eastem Gobi Desert, Mongolia. Ardynomys russelli sp. nov. is characterized by small size, brachyodont molars, and retention of P3. It represents the earliest record of the genus Ardynomys MATTHEW & GRANGER, 1925, in Asia. 

More than 400 paleontological type-specimens housed in the Montpellier University collections have been inventoried in this catalogue which includes charophytes, Paleozoic plants, brachiopodes, molluscs, arthropodes and vertebrates (selachians, amphibians, reptiles, birds and mammals). The vertebrates have been treated exhaustively in the catalogue and one can consider that it includes most of the type specimens deposited in the Montpelier II collections. 

The revision of the Rhombodontidae from the Maastrichtian of Morocco led us to the description of a new species: Rhombodus andriesi.

The biometrical study of populations of R. binkhorsti and R. microdon, species sometimes considered as synonymous, supports the conclusion that they represent two distinct species and not young and adult specimens of a single species. The stratigraphical range of these two species confirms this
result.

The reexarnination of type-series studied by C. Ararnbourg led us to revise the generic status of Rhombodus bondoni which is now ranged, because his dental features, in the new genus Dasyrhombodus showing a less derived dentition than Rhombodus. The stratigraphical range of each species is clarified within the phosphatic series. 

The geomyoid genus Dikkomys is well represented in a sample from the Black Bear Quarry Il local fauna of Early Hemingfordian age in Bennett County, South Dakota. Isolated unworn P/4's of Dikkomys matthewi WOOD have a prominent median cristid (sagicristid) with a connection to the metaconid and the hypolophid. With wear, P/4 does not become as molariform as P/4 because of this cristid.
A large sample of the Whitneyan beteromyid Proheteromys nebraskensis WOOD contains variants of the P/4 with on incipient sagicristid in approximately 18 percent of the population. The upper dentition and lower molars of Proheteromys nebraskensis are sufficiently generalized to indicate probable ancestry to Dikkomys. 

La poche de Ste-Néboule, commune de Béduer (Lot), 15 km environ à l'WSW de Figeac, fait partie du groupe le plus septentrional des gouffres creusés par les ruissellements du Paléogène dans les calcaires jurassiques de la bordure sud-ouest du Massif Central et qui furent comblés à la même époque par des argiles sidérolithiques accompagnées de phosphate de chaux concrétionné ainsi que des restes de la célèbre faune dite «des phosphorites du Quercy» . 

Bats are among the most numerous and widespread mammals today, but their fossil record is comparatively meagre and their early evolution poorly understood. Here we describe a new fossil bat from dental remains recovered from late Early Eocene sediments at Prémontré, northern France. This 50 million-year-old bat exhibits a mosaic of plesiomorphic and apomorphic dental features, including the presence of three lower premolars, a single-rooted p3, short p4 with metaconid, myotodont lower molars and a tall coronoid process of the dentary. This combination of features suggests it is an early member of Vespertilionidae, today’s most speciose and geographically widespread bat family. The Prémontré bat has bearing on hypotheses about the origins of vesper or evening bats (Family Vespertilionidae), as well as crown-group chiropterans.


  

The study of endocasts, or casts of the endocranial space, have played an important role in shaping understanding of mammalian, and particularly primate, brain evolution. Recently, the reconstructions of three-dimensional virtual endocasts from high-resolution computed tomography images have allowed for the visualization and quantification of endocasts in several Paleocene and Eocene primate species. Here we present the virtual endocast of MaPhQ 289 (informally known as the Montauban 9 skull), a specimen of Necrolemur antiquus Filhol 1873, a middle to late Eocene European primate of the family Microchoeridae. The virtual endocast of MaPhQ 289 reveals a lissencephalic surface morphology with expanded temporal poles and minimal overlap of the cerebellum or olfactory bulb by the cerebrum, which closely resembles the morphology of the endocast of its contemporary relative, Microchoerus erinaceus (Primates, Microchoeridae). MaPhQ 289 yields an endocranial volume (ECV) of 2.36 cm3, about 60% smaller than the volume of the most commonly cited ECV of N. antiquus. Thus, the size of the brain of N. antiquus relative to its body size is likely to be smaller than has been reported in previous literature, highlighting the importance of corroborating older ECV estimates with new evidence using 3-D imaging techniques. 

Morphological and biometrical description of skulls, teeth, and limb bones of extant and fossil Old World herniones (including E. hydruntinus) and of New World 'stilt-Iegged' and other slender species from Blancan to Holocene. An Appendix presents ways in which the approximate size of some missing bones or dimensions may be deduced from available ones.

The discussed and/or illustrated fossils were found in Bolivia (Tarija), Canada (Yukon), China (Choukoutien, Gulongshan, Jiling, Loufangzi), Ecuador (Oil Fields), Ethiopia (Melka Kunturé), France (Lunel-Viel), Germany (Süssenborn), Greece (Agios Georgios, Petralona), Hungary (Dorog), Italy (Romanelli), Mexico (Cedazo, San Josecito), Mongolia (Sjara-osso-gol), Spain (Venta Micena), ex-Soviet Union (Akhalkalaki, Binagady, Chokurcha, Chukochya, Kabazi, Kolyma, Krestovka, Kurtak, Staroselie, Tologoj), USA (Alaska, Arkalon, Cedar Meadow, Channing, Conkling, Dry Mountains, Hay Springs, Leisey Shell Pit A, Lissie Formation, Natural Trap, Pool Branch, Powers Ranch, Rock Creek, San Diego, Santo Domingo, Seymour Formation, Shelter, Slaton, Trinity River). Numerous raw or statistically elaborated data are given in Tables.

There is no evidence for the existence of Old World hemiones in the New World nor of 'stilt-Iegged' equids in the Old World. The first 'stilt-Iegged' equid was found at Santo Domingo, New Mexico, and is believed to be Late Blancan. It was probably at the origin of E. calobatus (Arkalon, Rock Creek) and of the smaller E. semiplicatus (Channing, Rock Creek). Slender, but not 'stilt-Iegged', equids found at Natural Trap, Wyoming, ca. 12 ky ago belong to Amerhippus. AlI these species share with Oid World Sussemiones (and some hemiones) peculiar patterns on the lower cheek teeth.

The slender Equus sp. B of Leisey Pit A, Florida, ca. 1.2 Ma, as weIl as Amerhippus francisci and E. tau (probably a senior synonym of E. quinni) share conventional lower cheek teeth patterns. The skulls of A. francisci and E. tau, however, are quite different.

Paleontological data suggest a common origin of Amerhippus, Sussemiones, and 'stilt-Iegged' equids during the late Blancan. Old World hemiones seem to have differentiated later. 

Description, for the first time, of the skull of Ruscinomys Depéret on the basis of a nearly complete specimen, and description of a new facial part of a Megacricetodon Fahlbusch skull (material from upper Miocene, Spain). New description of the skull (facial part) of " Cricetodon" incertum Schlosser on the basis of the specimen from the Oligocene of Quercy phosphorites already published by S. Schaub.
Comparison of the skull of “ C. ” incertum with that of the asiatic genus Cricetops Matthew and Granger and that of the North-American Eumys Leidy. These three genera of similar age display very distinct characteristics; their common origin must go back to the Eocene, as Wood believed.
Comparisons of the auditory regions of Ruscínomys and of Megacricetodon where important differences are noted. Comparison of the Cricetodontines from European Miocene with contemporary Cricetines. Contrary of the opinion held by Schaub, their anatomical differences do not seem suflicient to warrant the contention that none of the Cricetines derive from a form close to one of the known Cricetodontines. 

Monsieur René Lavocat, Directeur du Laboratoire de Paléontologie des Vertébrés de la troisième section de l'Ecole Pratique des Hautes Etudes, quittait le service actif en l'année 1979.
Cela fait maintenant quinze ans que fut installé à Montpellier, le laboratoire de Paléontologie des Vertébrés de l'Ecole Pratique des Hautes Etudes. La décision de M. René Lavocat a été particulièrement heureuse dans ses conséquences. Il a en effet permis le développement de l'enseignement et de la recherche en Paléontologie des Vertébrés à l'Université de Montpellier où se créa un des centres importants de cette discipline, en France. Il suscita la création de nouveaux laboratoires de l'Ecole Pratique des Hautes Etudes installés dès leur origine à Montpellier, ainsi que le déplacement à Montpellier d'un Laboratoire de l'Ecole Pratique, préexistant. Ce groupe de laboratoires constitue maintenant l'Institut de Montpellier de l'Ecole Pratique des Hautes Etudes.
[...] 

The genus Paraulacodus has been collected in the Ch'orora formation of Upper Miocene age, in Ethiopia. The new species, P. johanesi n. sp.. is more evolved than the previously described indian species P. indicus HINTON of the Siwalik Hills area. The morphological gap between P. johanesi and the present Thryonomys is still important. 

Two new Squalicorax species, S. benguerirensis nov. sp. and S. microserratus nov. sp. are described from the Lower Maastrichtian of the Benguérir phosphate open mine, Ganntour deposit, Morocco. The species S. benguerirensis nov. sp. was classically assigned to S. yangaensis since Arambourg (1952) and has been also recognized in coeval deposits from eastern USA to Mid-East. The species S. microserratus nov. sp. correspond to the lateral teeth of S. kaupi as reported by Arambourg (1952) and which is now referred in fact to S. bassanii. The comparison of these two new species with other Anacoracids, known in Moroccan or elsewhere, allows highlighting the great taxonomic and ecological diversities of this family during the Cretaceous.
  

Cranial anatomy of a late Miocene rhizomyid, Brafhyrhizomys cf. B. pilgrimi, provides new evidence on the origin of the dorsal, round infraorbital foramen of living rhizomyines. Primitive rhizomyids retain a myomorphous keyhole foramen with a long ventral slit that retracts upward during the evolutionary history of the Rhizomyidae. The primitive condition of the elongated ventral slit is represented by Kanisamys sivalensis. Among later burrowers the foramen shows progressive dorsal migration, the ventral slit terminating midway up the snout in B.tertracharax and B. choristos ; well above the midline of the snout in Brachyrhizamys cf. B. pilgrimi. Apparently this transformation began earlier among Rhizomyinae than among Tachyoryctinae and continued to a more derived stage in rhizomyines. ln living Rhizomyx the ventral slit is absent and only a high round hole remains at the anterior end of the zygomatic arch. 

Abstract not available 

The numerical importance of the Condylarths in the Cernaysian fauna is discussed. The Condylarth family, Tricuspiodontidae, is reviewed in the light of new material and its close relationships to the Phenacodontidae is suggested ; one new species is recognized : Tricuspiodon sobrinus. European Arctocyonidae are reviewed and the recentclassification of Van Valen is briefly commented on. Also,  the arctocyonine Landenodon is described for the first time in Thanetian (Late Paleocene) sediments ; two new species are proposed : T. lavocati and T. phelizoni. 

The Tertiary of the Salla-Luribay basin consists of red beds affected by the second period of the andine compression, of Miocene ending age. The Tertiary layers are exposed at an approximate elevation of 3.500 to 4.000 meters. Two stratigraphic units can be distinguished in them: the Luribay conglomerates, in which vertical clifts result from erosion, and the Salla layers consisting mostly of consolidated clays. These clays are very fossiliferous and have furnished a rich vertebrate fauna which gave to R. Hoffstetter the possibility to establish the Oligocene age of these beds. Sediments of same age has been reported to be present in several other places of Bolivia, particularly near Lacayani, where have been collected highly hypsodont Rodents, different from those found in Salla-Luribay basin. 

This paper proposes a systematic revision of the Oligocene Mongolian Ctenodactylidae, on the basis of abundant material obtained by screen/washing operations in stratified localities of the Ulantatal area (Inner Mongolia) (UTL1, 2, 3, 4, 5, 7, 6 & 8). A Chinese-German team has collected several thousands of isolated rodent teeth, and a number of fragmentary jaws. A new genus is identified (Alashania nov. gen. tengkoliensis nov. sp.), and eight former species are reevaluated, Karakoromys decessus, Tataromys sigmodon, T. minor, T. plicidens, Yindirtemys ulantatalensis, Y. bohlini, Y. deflexus, with several synonymies. A new Yindirtemys species is described: Y. shevyrevae nov. sp. and another one close to that: Y. aff. shevyrevae nov. sp. Four new species, which are rare in the localities, remain in open nomenclature because they are not well-represented. Yindirtemys differs from the other genera by the permanence of crescentic structures, while the other genera show a general reduction of the trigonoid area (= anterior valley). We define a range of size variation for each well documented population. Although the dental morphology shows a wide range of variation, given that transitional morphologies occur in a single locality, it is possible to provide a clear definition for most species. We show that dental patterns of the different genera can be derived from the pattern of Karakoromys. As a number of Tataromyinae have been determined in several localities from China, Kazakhstan and Mongolia, usually on the basis of scarce material, or surface collections, the present study would be used to re-evaluate their attribution inasmuch as the taxa are now placed in the Oligocene stratigraphy. The diversity of sizes and forms reflects the adaptive radiation of the family during the Oligocene, within a forested environment where the vegetation was probably abundant. 

The oldest european marsupials are described from some specimens (isolated upper molars) recently found from the Hainin sediment (Middle Paleocene of Belgium). These fossils document a new species of the Peradectes genus. They give evidence of a much older occurrence of the marsupials in Europe than it was assumed. They allow us to postulate a didelphid dispersal from South America towards the western-holarctic area operating in two phases : the first one of the Peradectes genus at the end of the Cretaceous; the second one of the Didelphíni tribe at the end of the Paleocene. A central american crossing is likely for the first one,  whereas a transafrican way is tentatively argued for the second one. 

ATLAS OF MESOZOIC AND CENOZOIC COASTLINES, par Alan G. SMITH, David G. SMITH & Brian M. FUNNELL, 1995. Cambridge University Press, 99 p., 31 cartes, 3 tab!., 2 fig. ISBN 0-521-45155-8.

L' "Atlas of Mesozoic and Cenozoic coastlines" succède avec bonheur aux "Mesozoic and Cenozoic paleocontinental maps" de Smith & Briden, publié en 1977. 

A new artiodactyl, Diacodexis antunesi n.sp., is described from the early Eocene of Silveirinha, Portugal. Comparisons are made with Diacodexis gazini GODINOT, 1978, D. varleti SUDRE et al., 1983, D. cf. varleti from Paris Basin sites, D. sp. from Dormaal and from localities in Spain and England, D. secans from North America and D. pakistanensis from Asia; affinities and evolutive tendencies are discussed. The presence of Diacodexis in the locality of Silveirinha confirms the very early Eocene age of the latter. As Diacodexis antunesi appears ta be more primitive than D. gazini from Rians (early Eocene of France), it lends corroboration to the interpretation (essentially based previously on condylarths) of the Silveirinha assemblage as the oldest Eocene fauna known in Europe and supports the hypothesis that early artiodactyls migrated from Europe to North America.