The description of new material of the Upper Eoœne of France, Southem Germany and Spain together with the restudy of the material described by Thaler (1966b) as Pairomys allows to confirm the validity of the genus Ectropomys up to know controversally discussed. As a consequence the subfamily Remyinae and Oltinomyinae can be defined precisely. The study of the dental characters shows that the Remyinae in fact belong to the Theridomyidae and represent a derived evolutionary unit within this family. The Oltinomyinae together with the Theridomyinae and Issiodoromyinae very probably form a monophyletic unit. 

In the course of a revision of the Equoidea numerous dentitions as well as a partial skeleton of a Phenaeodont were discovered from the Middle Eocene lignite beds of the Geiseltal locality. These fossils are recognized as a new genus and species of Phenacodontidae : HaIlensia matthesi n.g. n.sp.. The species is present in the « untere und obere Unterkohle ›› (uUK, oUK = the lower and upper part of the Lower Coal Seam) as well as in the « obere Mittelkohle ›› (oMK = the upper part of the Middle Coal Seam). Two fragmentary upper jaws described and figured by Matthes (1977) as Propachynolophus gaudryi are also belonging to Hallensia matthesi. Thus the decisive argument for classifying the " Unterkohle " of the Geiseltal section as Lower Eocene has to be dropped. Another relict form of the Geiseltal is Esthonyx tardus n. sp. documented by a fragmentary mandible coming from the « untere Unterkohle ››. This is the latest Tillodont from Europe. Contrasting to E. munieri from the european Lower Eocene the dentition of E. tardus is morphologically more progressive. 

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. 

Some complete tooth rows and about one hundred isolated teeth enabled the identification of the deinothere of the Vallesian site Montredon (Hérault) as Deinotherium giganteum KAUP 1829, mainly by comparisons with the likewise Vallesian sample of the type locality Eppelsheim (Rheinhessen, F.R.G.).
Scatterdiagrams of the teeth show the importance of allometry during the phyletic size increase of the European deinotheres.
Some taphonomic problems of the Montredon deinothere are briefly mentioned. 

The study of all the available skulls allows us to review the systematic relationships of the longirostrine Steneosaurus from the Middle Jurassic of western Europe. Up to now, Aalenian and Bajocian deposits have not yielded any significant Steneosaurus remain. In the Bathonian, the only valid longirostrine species, S. megistorhynchus, is known in the Britain-Normandy Basin, the Poitou and the Lorraine. In the Callovian, most of the longirostrine Steneosaurus remains can be attributed to the species S. leedsi. Nevertheless, some remains from the Middle Callovian of Poitou (France) show important differences with S. leedsi. A new Steneosaurus species, only known in Poitou, is created and named S. pictaviensis. The specific characters are carried by the skull (preorbital pit well marked, orbit and ptetygoid fossae shapes), by the mandible (symphysis shape) and by the teeth (ornamentation). S. megistorhynchus is probably situated near the stem of the Callovian species but remains from the Bathonian and Lower Callovian are very scarce and it is very difficult to precise the phylogenetic relationships between the longirostrine species of the Middle Jurassic.
  

The late Cretaceous Auca Mahuevo nesting site (Neuquén Province, Argentina) has produced a large number of sauropod eggs, many of them containing the remains of embryos. Research at this site has generated important information about the development of the embryos, the morphology and eggshell microstructure of the eggs, and the reproductive behavior of sauropod dinosaurs. Cranial features present in the embryos have allowed their identification as those of titanosaurian sauropods. Differences in the texture of the sediments that contain some of the egg-clutches have illuminated their nest architecture. Microstructural studies of eggshells have expanded our knowledge of their variability and the incidence of pathologies within a reproductive titanosaurian population. Maps showing the spatial distribution of eggs and clutches. the stratigraphic distribution of the egg-beds, and the sedimentological context in which they are contained, have provided the basis for several inferences about the nesting behavior of these dinosaurs. 

The review of material recently collected in the new localities from the “Phosphorites du Quercy", and different localities from the South of France, bring new informations on the genus Eucricetodon THALER. 1966, and Pseudocricetodon  THALER,  I969 (Middle and Upper Oligocene. Western Europe). Thanks to Eucricetodon huerzeleri VIANEY-LIAUD, 1972, which were unsufficiently known until now, is proposed. During the middle Oligocene Eucricetodon atavus  MISONNE, 1957 seems to give rise to two lineages. One of them led to Eucricetodon huberi,which however exhibits a larger size and a development of progressive characters on the teeth. The other would be Eucricetodon huerzeleri well differentiated at the “Mas de Pauffié" standard level (beginning of the upper Oligocene). The ornementation of lower incisors is described, when possible. Though the fossils are not abundant, it seems that the ancestral lineage, Eucriretodon atavus, remains in  the upper Oligocene (Boningen standard level). evolving into Eucricetodon praecursor SCHAUB, 1925 (Rickenbach standard level). The characters of Eucricetodon dubius  (SCHAUB. 1925), represented by a numerous population in Pech Desse and Pech du Fraysse (Quercy). confirm that this species and Eucricetodon praecursor  belong to two different lineages. As Eucricetodon dubius shows more primitive features, this species could not originale from Eucricetodon atavus -Eucricetodon huberi. The appearance of this species at the level of Mas de Pauffié could be the result of an immigration. A new definition of Pseudocricetodon incertus (SCHLOSSER. 1884) is given. This species has been found in several localities, where it had not been identified until now. lts comparison with Pseudocricetodon moguntiacus  (BAHLO. l975), found at several localities from the standard level of Antoingt (end of middle Oligocene). shows a parallel evolution to that of Pseudocetodon incertus, which is  of larger size and with a less complicated pattern of teeth. 

The Montredon local fauna yielded very rare bats, represented by damaged isolated teeth. Only a few documents are available for this period of the European Neogene. ln this poor state of knowledge, the material represents three undetermined species, a supposed molossid and two vespertilionids. 

The rodents (Cricetidae, Gliridae, Sciuridae) found in lacustrine, brackish marine and karstic sediments of Miocene age in Languedoc, assign the position of the different localities in the scale of "niveaux repères" used by mammalogists. Some detailed stratigraphical studies bring several correlations between this continental biochronological scale and the marine scale ; the most important results are the Aquitanian age of the "niveaux repères" of Coderet and Paulhiac, the Burdigalian age of Laugnac, Estrepouy, Vieux-Collonges, La Romieu and Sansan and the Langhian or Lower Serravallian age of La Grive M. The correlations between the Tethys and the Central Paratethys for the Lower Neogene profit also of these results, since the locality of Neudorf Spalte 1, 2 (Czechoslovakia) is shown to be younger than Sansan (France). The paleontological study has also several geological inferences for the Miocene of Languedoc ; with the calibration of this Miocene, we know quite precisely that the Lower Miocene is chiefly a time lacustrine sedimentation, and also that the marine Miocene sedimentation ends early in the Miocene Period, in Langhian or lower Serravallian times. 

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. 

Three new fossiliferous localities, two of karstic origin, Castelnou 3 and Font Estramar, respectively Late Upper Miocene and Lower Pliocene, and one of lacustrine origin, Thuir, Lower Pliocene, add data about the transition between Miocene and Pliocene faunas of rodents in southern France. An unexpected association of taxa was present in the late Upper Miocene, including between others, Myocricetodon, Hispanomys, Ruscinomys, Cricetus barrierei, Promimomys and a new species of Stephanomys, S. dubari nov. sp. Myocricetodon is still known in the Lower Pliocene. It is shown that the large field-mice known since the Late Upper Miocene belong to two different lineages, on one side, A. jeanteti, on the other side, A. gudrunae followed by A. gorafensis. Biochronological and biogeographical implications are discussed. 

The eggshell of Nicobar scrubfowl (Megapodius nicobariensis) is described for the first time. Its egg porosity is calculated and discussed with data from several taxa (another megapode, some extant and fossil reptiles including a titanosaur group) in order to compare incubation types with eggshell structure. Eggshell microstructure reflects first phylogenetic traits and does not seem to have developed major adaptative features due to the incubation conditions, except for the pore canals. 

Micro-CT imaging is an increasingly popular method in paleontology giving access to internal structures with a high resolution and without destroying precious specimens. However, its potential for the study of hypoplasia defects has only recently been investigated. Here, we propose a preliminary study to test whether hypoplastic defects can be detected with micro-CT (μCT) scan and we assess the costs and benefits of using this method instead of naked eye. To do so, we studied 13 fossil rhinocerotid teeth bearing hypoplasia from Béon 1 (late early Miocene, Southwestern France) as positive control and 11 teeth of the amynodontid Cadurcotherium (Oligocene, Phosphorites du Quercy, Southwestern France), for which enamel was partly or totally obscured by cement. We showed that all macroscopically-spotted defects were retrieved on 3D reconstructions and selected virtual slices. We also detected additional defects using μCT scan compared to naked eye identification. The number of defects detected using μCT was greater in the Cadurcotherium dataset (paired-sample Wilcoxon test, p-value = 0.02724) but not for our control sample (paired-sample Wilcoxon test, p-value = 0.1171). Moreover, it allowed for measuring width and depth of the defects on virtual slices (sometimes linked to stress duration and severity, respectively), which we could not do macroscopically. As μCT imaging is both expensive and time consuming while not drastically improving the results, we recommend a moderate and thoughtful use of this method for hypoplasia investigations, restricted for instance to teeth for which enamel surface is obscured (presence of cement, uncomplete preparation, or unerupted germs). 

The early gnathostome genus Mesacanthus is well represented in both Lower Old Red Sandstone and Middle Old Red Sandstone assemblages of northern and central Scotland. This ‘acanthodian’ taxon is currently thought to comprise two valid species: M. mitchelli and M. pusillus. Although the whereabouts of the holotype of M. mitchelli (NHMUK PV P560) is known, the syntype material for M. pusillus has long been thought lost. Here we identify at least one specimen that formed part of the original syntype material for M. pusillus, albeit in a slightly different condition than when it was originally figured. This specimen is ROM 25872, which is here designated as the lectotype. A second specimen – ELGNM 1978.191.1 – could represent another of the syntype specimens, but poor preservation quality makes it impossible to be certain. 

The origin and early evolutionary history of the dinosaurs is a topic that has recently gone through a period of renewed interest and academic debate. For 130 years, one way of classifying the various dinosaur subgroups persisted as the accepted model, with increasing levels of research in the past quarter-century also providing evidence for the hypothesis that dinosaur origination occurred in the Southern Hemisphere, particularly in South America. It is, after all, from within the Late Triassic strata of countries like Argentina and Brazil that we get some of the very best early dinosaur specimens; many of these specimens are the earliest known representatives of some of the major dinosaur subgroups, such as the theropods and sauropodomorphs. However, some recent analyses have brought about a shift in terms of what is currently accepted and what is now disputed regarding the origin of dinosaurs – the Southern Hemisphere origination hypothesis was questioned (although this was based upon observations and not with quantitative analysis techniques), as has the shape of the dinosaur tree. Responses to the new hypothesis were numerous; many further supported a Southern Hemisphere point of origin. Whilst the interrelationships between the major dinosaur clades remains to be resolved, the current data does seem to comprehensively answer the question of where the dinosaurs first originated. However, it is arguable whether the current data that is being used in such palaeobiogeographical analyses is sufficient to provide an answer to the question of where specifically the dinosaur clade first appeared. This short communication urges a degree of caution about the current consensus and what steps may need to be taken to ensure that more meaningful results are produced in the future. 

The presence of cambaytheres, the sister group of perissodactyls, in western India near or before the time of collision with Asia suggests that Perissodactyla may have originated on the Indian Plate during its final drift towards Asia. Herein we reinforce this hypothesis by reporting two teeth of the first early Eocene tapiromorph Perissodactyla from the Cambay Shale Formation of Vastan Lignite Mine (c. 54.5 Ma), Gujarat, western India, which we allocate to a new genus and species, Vastanolophus holbrooki. It presents plesiomorphic characters typical of the paraphyletic “Isectolophidae,” such as small size and weak lophodonty. However, the weaker hypoconulid and low paralophid, higher cusps, lower cristid obliqua, and the lingual opening of the talonid are found in Helaletidae, the most primitive tapiroid family. V. holbrooki, gen. et sp. nov., may be the oldest and the most primitive tapiroid, suggesting that at least tapiroid perissodactyls originated on India. 

Les Mammifères post-glaciaires de Corse de Jean-Denis Vigne, étudie l'évolution des mammifères en Corse depuis 7000 av. J.-C. jusqu'à aujourd'hui, en explorant leur adaptation insulaire, l'impact de l'homme sur leur extinction ou leur introduction, et les pratiques de chasse et d'élevage à travers l'analyse des ossements. 

The discovery in the Turolian (Late Miocene) of Dytiko 3 (Macedonia, Greece) of a complete skull with mandibles and cervical vertebrae, atlas and epistropheus, is a very important contribution to the knowledge of the subfarnily Chalicotheríinae. After the description, the comparison with other specimens of Miocene chalicotheres permits the revival of the generic name Macrotherium with a new species M. macedonicum. This genus is mainly characterized by a short snout and an inflated cerebral skull. It coexists during the Miocene with Chalicotherium. A cladistic analysis leads to conclusion that the species which has been described from the Early Middle Miocene of Rusinga must be identified as the type-species of a new genus: Butleria.





  

The fossil mammals collected from the Eocene of Hammada du Dra (northwest Sahara. Algeria) and two fragmentary teeth from the Lutetian of M'Bodione Dadere (Senegal) are described.
The fossils from the northwest Sahara come from a lacustrian deposit dated by charophytes (Raskyella aff. pecki, Raskyella n. sp.. Maedleriella lavocati, Maedleriella sp. et ? Peckichara sp.) as Middle Eocene or perhaps Lower Eocene (Gevin, Feist and Mongereau, 1974). Several hyracoids (3 or 4) identified from this formation extends the age of the family Pliohyracidae Osborn in Africa. Three forms appear to belong in the genera Megalohyrax, Titanohyrax and perhaps Bunohyrax which have been know until now only from the lower Oligocene of the Fayum (M. gevini n. sp. ; T. mongereaui n. sp.. ? Bunohyrax or Megalohyrax indet.). Another hyracoidof small size is referred to a new genus, Microhyrax (M. lavocati n. sp.).
Helioseus insolitus n. g. n. sp. is described without ordinal assignment. Azibius (Sudre, 1975) which has been the subject of questions and interpretations is reviewed.
Only one tooth from the Lutetian of M'Bodione Dadere is complete enough to interpret. lt probably belongs to a condylarth and demonstrates for the first time, the presence of the order in Africa. The second tooth is too fragmentary for comment.
In conclusion., the paleobiogeographic role of Africa at the end of the cretaceous and the beginning of the Cenozoic is discussed. 

Until now Aplodontidae of the European Oligocene have been documented by four species only. The phylogenetic relations remained obscure. as the distribution of only one species has been known in some detail. New material made it possible to define the stratigraphic range of two of the already existing species (Plesispermophilus angustidens, Sciurodon cadurcense) and to follow their development during the Oligocene beginning with the event of the « Grande Coupure ››. Sciurodon remained nearly without change until the end of the Middle Oligocene. Plesispermophilus angustidens split into two distinct phyletic lines, one of which (P. macrodon n. sp.) reaching considerable size, is represented till the beginning of the Upper Oligocene (Pech de Fraysse, Gaimersheim). The other line leads to Plesispermophilus ernii (basal Upper Oligocene of Burgmagerbein 1. terminal Upper Oligocene of Coderet). Besides the already known forms a new small-sized species (P. atavus n. sp.) is described, which by its primitive features closely resembles the genus Plesispermophilus. Two other small-sized species already known from the Upper Oligocene (? P. argoviensis) and Lower Miocene (? P. descedens) seem to be closely related to the new species. It cannot be decided whether they are descendents of this line or have developed independently, because of their poor fossil record.
Comparison of the evolutionary modalities in the different phylogenetic lines reveals general trends. the most striking of which is the complication of the tooth pattern by the development of additional crests. In the lower molars the cusps diminuate in size and are more and more transformed into ridges. ln addition new connection between the crests appear. in the upper molars, the « selenodont » shape of the teeth becomes more and more dominant, and in the two main evolutionary lines of Plesispermophilus the metaconulus becomes duplicated. A further evolutionary trend is the size increase of the premolars compared to the molars, which is even more pronounced in the Miocene Aplodontidae.
Phylogenetic relations between the primitive Plesispermophilus and certain « prociurines ›› of Northern America as well as between Plesispermophilus (P. angustidens) and more progressive forms of the Upper Oligocene (P. ernii, P. macrodon n. sp.) can be documented. In this light, the taxonomic distinction between Prosciurinae (bunodont) and Allomyinae (selenodont) sensu Rensberger 1976 can be shown to be artificial, because it separates forms from each other, which are evidently closely related. Consequently the separation into two subfamilies has been abolished.