Two new species, Omanodon minor n. g., n. sp. and Shizarodon dhofarensis n. g., n. sp., known from fifteen isolated teeth, are described here as the first adapiform primates (?Anchomomyini) recognizable to date in the Taqah material (early Oligocene of Sultanate of Oman).

Omanodon minor n. g., n. sp. displays special morphological similarity to the adapid tribe Anchomomyini from the Eocene of Europe, and especially to the Anchomomys lineage. Resemblances with the extant lemurifonn Microcebus are also noticeable and could be regarded as supporting Schwartz & Tattersall (1983) hypothesis of special relationships between the anchomomyine adapids and the cheirogaleid lemuriformes. However, these morphological affmities can be interpreted, altematively, as the results of parallelisms: important differences in upper molars indicate that the resemblances of cheirogaleids and Omanodon minor n. g., n. sp. are indeed probably due to parallelisms. Phyletic relationship of O. minor n. g., n. sp. to Anchomomyini is finally the most likely hypothesis.

Shizarodon dhofarensis n. g., n. sp., although much more poorly known, is closely related to Omanodon minor n. g., n. sp., at least at a familial level. The general morphology of this species suggests
also a close link with adapid Anchomomyini, although precise relationships within this tribe remain obscure. Interesting resemblances of Shizarodon dhofarensis n. g., n. sp. to Djebelemur martinezi lower molars (early Eocene of Tunisia) are also noticeable. These resemblances are even stronger than those betwen Omanodon minor and Djebelemur martinezi. However the very bunodont upper molars referred to D. martinezi are unusual for adapids, and there are moreover some notable differences in their lower molars. Thus resemblances in Djebelemur and Shizarodon are probably due to paralellisms.

Because of the fragmentary nature of the material and of possible parallelisms, the systematic position of Omanodon and Shizarodon within adapiformes cannot however yet be established definitively. 

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.





  

Rodents from the new localities of Châteauredon (Alpes-de-Haute-Provence) and La Denise (Bouches-du-Rhône) show more similarities with the rodents known from the Czecho-Slovak locality of Franzenbad than with the species found in contemporaneous Lower Miocene faunas located westward of the present Rhône Valley. This is another data wich support the existance of several biogeographical provinces in Southern France during Lower Miocene. The correlations which have been settled down allow new datations of several formations in Provence and give new information on the Aquitanian and Burdigalian paleogeographies of this region. More precise stratigraphical allocations are given to some other localities of Central Europe. 

The faunal list of the mammals collected at the locality of Aumelas (Hérault, France) is revised. For the first
time this Middle Eocene locality is precisely settled in the european chronological scale of "niveaux repères", between the levels of Bouxwiller and Egerkingen, in Uppermost Lutetian.
A new Dichobunid from the site is described : Aumelasia gabineaudi n. g., n. sp. This new genus has primitive characters. and it may be in the descent of the Lower Eocene Protodichobune. 

Pangolins have never shown a high taxic diversity and their fossil record is scarce. We report here the first discovery of a partial humerus from late Oligocene deposits in Pech du Fraysse (MP28, France). The new specimen from Pech du Fraysse is described and compared to various extant and extinct species of pangolins. It shows a suite of morphological features very similar to the humeri discovered in Saint-André (MP 26), Solnhofen (Burdigalien), and Saulcet (Aquitanian), attributed here to Necromanis franconica. The description of the specimen from Pech du Fraysse allowed us to discuss the systematics of Paleogene and Neogene pholidotans. The differences between PFY 4051 and N. franconica on the one side, and N. quercyi on the other side, might be sufficiently important to justify a generic distinction. A comparison with extant species showed that N. franconica was likely terrestrial and fossorial based on its humeral morphology. 

A new example of parallelism in the dental pattern ofthe Theridomyidae is illustrated by the description ofa new species: Theridomys Iudensis from the standard level of Antoingt (middle Oligocene). Considering the occurence ofthis parallelism phenomenon. the use of numerous qualitative and quantitative criteria is essential to characterize the different stages ofthe different evolutive lineages. Thus, a new simple parameter is proposed (CHY = H+l/0,5 L) to estimate hypsodonty of the medium hypsodont Rodentia. 

A new species, Otonycteris rummeli nov. sp., is described from the Late Miocene site Gritsev (MN 9) in the Ukraine. Otonycteris rummeli nov. sp. differs from those of most vespertilionids, except recent Otonycteris, Antrozous and Early Miocene Karstala silva, in having a well-developed entocingulid at the foot of the trigonid valley in the lower molars. The morphological resemblance of Otonycteris, Antrozous and Karstala is apparently a case of convergence in the evolution of the Old and New Worlds bat faunas. From at least the Middle Miocene the range of Otonycteris distribution spread to the whole of Central Europe and such a situation continued during the whole Late Miocene. This indicates a more arid climate in Europe during the Upper Miocene compared to the Quaternary. The reduction of the distribution range of Otonycteris and its extinction in most of the territory of Europe could have been caused by the global climatic cooling and increasing glacial cycle amplitude during the onset of the Quaternary. 

The utilization of screen-washing and attack by dilute acetic acid has permitted the collecting, in the Miocene of the department of Hérault (France), of a very rich ichthyofauna. This fauna is presently comprised of about 60 studied species, of which 11 are new, and represents, in the present state of knowledge, the most varied Miocene selachian fauna described in the world.
The abondance of material has allowed an overall revision to be made; it has thus been possible to complete the description and the figuration of species that were poorly known until now, and to synonymize species that were established on simple morphotypes. Paleo-ecologic study of the ichthyofauna has permitted conclusions to be drawn relative to climate and bathymetry; it was thus possible to show that the Miocene fauna of Hérault was a fauna of a subtropical sea, essentially neritic with rare pelagic contributions.
Knowing the stratigraphic position of the localities, it has been possible to distinguish three faunal assemblages based on associations of species. Some hypotheses on the evolution of certain lineages have been expressed.
The comparison of this fauna with that of other regions permitted the relationships of two diflerent faunal provinces to be specified: the first belongs to the northern domain, characterized by a fauna still subtropical but with numerous temperate water elements; the leoond belongs to the Mesogean domain characterized by warm water forms. It has also lhovm that contemporary faunas could be very different according to the bathymetric zone in which they lived, which furnishes valuable information for the paleogeographic reconstruction of sedimentary basins.
  

An upper giraffid premolar without any indication about its origin is preserved at the Montpellier University among numerous fossils from the ruscinian formation of Montpellier. It can be related to Samotherium, of the Upper Miocene in Eastern Europe, North Africa and Asia, or more probably to Bramatherium  or Hydaspitherium of the Pliocene of South East Asia. The sedimentological study of the matrix shows a calcareous background, which may indicate that this tooth does not come from the Montpellier formation. 

The intensive exploration of the Pliocene Hadar Formation, rich in hominid remains, led us to the discovery of several micromammals levels. ln some of them, rodents are very abundant. The stratigraphic repartition of these levels do not cover the whole fossiliferous series of the formation but takes place only in the sedimentary members from Sidi Hakoma and Denen-Dora (rancing from 3.1 - 3.2 MY to 2.8 - 2.9 MY, according to the recent geochronological data). During this gap of time, the species do not show morphological changes, what allowed us to gather, in the same taxa, forms of slighty different ages.
Two striking facts, giving a lot of indications, characterize these small rodents'faunas. First, we notice the domination of the Muridae, as well on a qualitative way (number of species) as on a quantitative one (number of individuals). Then, it appears that, until now, two genera of these murids were known only in the south-western asiatic regions. So, we can suppose continuous biotops between Africa and Indian Subcontinent before 3 MY. In this hypothesis, the hominids had already the possibility to leave their african « cradle ››. Finally, almost all studied genera are still represented at the present time. This fact, previously observed in Laetolil, Omo, Olduvai contributes to remove hope of establishing a biochronological scale based on rodents, in tropical zone. Nethertheless, that allows to try a reconstruction of the palaeoenvironnement, by using the principle of actualism.
  

The anatomy of Norselaspis glacialis n.g., n.sp., a primitive kiaeraspidian from the Lower Devonian of Spitsbergen, is described on the basis of spécimens studied by grinding sections or prepared with dilute formic acid. This study yielded some new anatomical details, including the presence of a canal prolonging posteromedially the canal alloted to the facial nerve by Stensiö. This posterior prolongation of the « facial canal ›› into the posterolateral part of the labyrinth cavity is consistent with the hypothesis put forward by Allis, Lindström, Jefferies and Whiting, that this canal housed the glossopharyngeus nerve. Furthermore, in N. glacialis, the foramen usually referred to as the foramen for the œsophagus opens posteriorly into a cavity in the postbranchial wall, referred to here as the intramural cavity, and which is interpreted as having housed the heart. Consequently, the œsophagus probably accompanied the dorsal aorta through the aortic canal. Finally, the foramen generally interpreted as having transmitted the ventral afferent arterial trunk is here considered as having housed the hepatic vein, which emptied into the venous sinus of the heart. The ventral afferent arterial trunk may thus have passed through the former «œsophageal ›› foramen.
The problem of the position of the dorsal nerves in the Osteostraci is discussed, and it is suggested that the three foremost nerve canals opening into the oralobranchial cavity housed the maxillary ramus of the trigeminus, the facial nerve and the glossopharyngeus nerve respectively. The mandibular ramus of the trigeminus must have accompanied one of the two foremost nerves, but for the moment it is impossible to decide which.
The problem of the nature of the interbranchial crests of the Osteostraci is briefly discussed. Comparison with the branchial apparatus of the Petromyzontida does not support the hypothesis that the interbranchial crests are part of the branchial arches, incorporated into the endoskeletal shield. A different hypothesis is proposed, that the branchial skeleton of the Osteostraci was situated entirely inside the oralobranchial cavity, and was attached to the endoskeletal shield only by the ventromedial processes. The grooves classically allotted to the efferent branchial arteries would thus have housed extrabranchial arteries, branching off from the dorsal aorta, and irrigating the ventral branchial musculature.
A phylogeny and a classification of the kiaeraspidians are proposed. The evolution of this monophyletic group is characterized by, e.g., reduction of cornual processes, shortening of the abdominal division of the shield, subdivision of the lateral fields, and enlargement of the supraoral fossae.
The phylogenetic position of the kiaeraspidians within the Osteostraci remains uncertain. Their sister-group may be either the benneviaspidiens or the thyestidians, or Thyestes alone (in which case they would have to be included within the thyestidians). 

The genus Pachynolophus, one of the poorest known of the Palaeotheriidae, includes the brachyodont forms with reduced and non-molariform premolars and with upper molars lacking a mesostyle. Quantitative characters (divers surface indications and elongation of the teeth), while demonstrating a close relationship to Hyracotherium, permit a better differentiation of the genus, confirm its specific splitting, and permit the distinction of three lineages. The skull from Memerlein is taken as the type of a new species, P. Iavocati, of which the dentition is extremely characterized by its lophiodonty, the strong reduction of the premolars and the reduction of the cingula. This characterization testifies to a late age which extends the existence of the genus quite near to the Eocene-Oligocene limit. Compared with the only two skulls known of related species (Hyracotheríum vulpiceps and Pachynolophus Iivinierensis), that from Memerlein is distinguished by progressive characters affecting diferent regions but most particularly the braincase; it is not possible, however, to isolate within this evolution the part which leads to a systematic differentiation. Modernization is translated by a considerable increase in size of the braincase, principally in the frontal region, a development of the facial region with anterior displacement of the dental series and a greater specialization of the masticatory apparatus. This evolution parallels the history of the Equidae of the North American early Tertiary, but certain particularities, the form of the alisphenoid, the presence of an anterior frontal foramen, and the structure of the paroccipital apophysis, testifies to the independance of the European forms. 

The first part of this study was devoted to a descriptive analysis of teeth morphologies among the vespertilionine bats. This leads now to a tentative synthesis, providing views on the systematics of the group. The results could be seen according to three distinct but closely related purposes : 1 - the sorting of the genera contents in order to conform the genera units to homogeneous taxa that could represent natural issues of evolutionary lineages ; 2 - the investigation of relationships between extant genera in order to infer the possibilities of common origin ; 3 - according to the preceeding items and to the observed evolutionary trends, a tentative phylogeny, modest and cautious. The contents of many genera are sorted : Leuconoe is removed from subgeneric to generic position, whereas Myotis becomes a subgenus of it ; the myotodont species are cleared away from the Pipistrellus genus ; Glischropus and Scotozous are synonymized within Pipistrellus ; Hypsugo is raised to the generic level ; some species previously ranged within Pipistrellus will form provisionally a collective group, Attalepharca nov. ; the Eptesicus genus is broken up, the excluded species being grouped within Nycterikaupius gen. nov. ; the Nycticeini tribe is defined again after exclusion of Otonycteris , Scotoecus, Scotophilus , and addition of Hesperoptenus ; the species la io and Pipistrellus tasmaniensis are removed to Eptesicus (n.s.) and Pipistrellus dormeri to Scotoecus. Groupings of genera are stated according to the main evolutionary trends of I1/. The relevance of these is often warranted by close morphologic similarities of other teeth. This leads to a recognition of the major evolutionary radiations which occurred in the group. The filiations schematized at the end of the work show the dental relationships observed between the extant genera, and could represent a phylogenic framework. Two major facts are to be underlined : 1- the early divergence of leuconoids ; 2 - the successives crossings to myotodonty from the nyctaloid flow. Fossil data from the literature are punctually and tentatively incorporated within phylogenic sketches. 

    Two families are reviewed (Hyracodontidae and Rhinocerotidae) from the Paleogene of Mongolia. The following taxa are described from the former family:  Triplopus? mergenensis sp. nov., Prohyracodon meridionale CHOW, Prohyracodon? parvus sp. nov., Forstercooperia ergiliinensis GABUNIA & DASHZEVEG, Ardynia praecox MATTHEW & GRANGER, A. mongoliensis (BELIAYEVA), Ardynia sp., Urtinotheríum sp. (or Indricotherium) and Armania asiana GABUNIA & DASHZEVEG. All of them are from the Paleogene of the eastem Gobi Desert The hyracodontid Pataecops parvus RADINSKY is described from a new locality, Menkhen-Teg (Middle Eocene), in the Valley of Lakes.
    In the second family, a new species of Ronzotherium, R. orientale sp. nov. has been recognized from the Oligocene of Ergilin Dzo and Khoer Dzan of the eastem Gobi Desert. Ronzotherium sp. and Allacerops sp. have been described from the Oligocene of Khoer Dzan. The genus Ronzotherium, formerly known from the Oligocene of eastem Europe, has been reliably established in the Oligocene fauna of Mongolia. The genus Symphysorrachis BELIAYEVA, 1954, previously believed to be a junior synonym of Ronzotherium, is here resurrected.
    Descriptions are provided for key localities in the Eocene and Oligocene of Mongolia and the adjacent territories of northern China, containing fossil Hyracodontidae and Rhinocerotidae. In addition, the question of the Eocene-Oligocene boundary in these Mongolian and Chinese sections is discussed. Paleontological evidence has been used to correlate Eocene-Oligocene boundary layers in the eastem Gobi Desert (Mongolia) and Inner Mongolia (China). A brief discussion is provided on the phylogenetic affinities of the genera within the family Hyracodontidae. 

A fossil species of the extant genus Leuconoe, L. lavocati n. sp. from Le Garouillas Oligocene locality, Quercy phosphorites, SW-France, is established in nomenclatural standards. 

Fourteen distinct phyletical lineages which belong at least in three families: Ischyromyidae ALSTON, 1876, Gliridae THOMAS, 1896 and Theridomyidae ALSTON, 1876, have been identified after the study of more than 3600 rodent dental remains from about twenty Early and Middle Eocene european localities. A systematical and phylogenetical revision of these rodents has been achieved. Nearly all the specific and generic diagnosis are emended. Several new combinations and synonymies are proposed. Four new species and two new genera, Euromys nov. (Ailuravinae) and Hartenbergeromys nov. (Microparamyini), are named and described. Euromys nov. gen. is known by three distinctive ypresian (MP 7 to MP 10 european reference levels) chronospecies. This new lineage is thought to be the direct ancestor of Meldimys MICHAUX, 1968 and Ailuravus RUTIMEYER, 1891. A new species of the genus Plesiarctomys BRAVARD, 1850, Pl. lapicidinarum from Condé-en-Brie (MP 8-9 reference level), allows to relate the Plesiarctomys lineage to the Pseudoparamys MICHAUX, 1964 one. The taxa Sparnacomys HARTENBERGER, 1971, Pantrogna HARTENBERGER, 1971, and Corbarimys MARANDAT, 1989 are erected to genus rank; the last one is not thought to be an Ischyromyidae. A new chronospecies of Pantrogna, P. marandati nov. sp. from the locality of Prémontré (MP 10 reference level), is described. This lineage is at the origin of two others, namely Masillamys TOBIEN, 1954, including M. mattaueri (HARTENBERGER, 1975) nov. comb. (MP 10 reference level), and Hartenbergeromys nov. gen., known from MP 10 (H. hautefeuillei nov. sp.) and MP 11 (H. parvus TOBIEN, 1954) reference levels. The phylogenetical position of Hartenbergeromys nov. gen., at the origin of the european family Theridomyidae, is discussed. The systematical and phylogenetical status of two probable Paramyinae, "Paramys" woodi MICHAUX, 1964 and an unnamed genus and species, are discussed. New populations of the primitive Gliridae Eogliravus HARTENBERGER, 1971 and of the primitive Theridomyidae Protadelomys HARTENBERGER, 1968, are described and assigned to previously known species.

  

The composition of assemblages of lizards and Amphisbaenian from the European Eocene are described. At least ten lizard families are identified from the lower European Eocene levels. Eight are still recorded in the last level (Escamps) of the late Eocene. Agamid lizards (genus Tinosaurus) died out by the end of the lower Eocene and Varanid lizards (genus Saniwa) disappeared by the beginning of the late Eocene. Amphisbaenians are recorded throughout the Eocene in Europe. The lacertilian fossil record of Europe and North America show a high degree of faunal resemblance in the early Eocene, followed by a decrease during the later part of the epoch. The lacertilian and amphisbaenian faunas from the European Eocene are not subject to great variations during the period; this is in contrast with the mammal record at the same time. It is argued that the low metabolic rates and the ectothermy of lizards could explain those differences, along with the increasing insularity of the West European area during the late Eocene time.

  

The present study of Artiodactyla from the Middle Eocene of the Geiseltal lignite beds concems systematics, biostratigraphy, and palaeoecology on the basis of 174 specimens: isolated remains to more complete skeletons. Instead of the formerly known five species of two families are now recognized 14 species of the Diacodexeidae, Dichobunidae, Cebochoeridae, and Haplobunodontidae. New species are Aumelasia maniai, Anthracobunodon neumarkensis, Masillabune franzeni. Four species of the Geiseltalfauna are definitely known from elswere, and five species are closely related to those from other European localities. Evidently the faunal situation of artiodactyls during the Middle Eocene of Europe was largely uniform. The distribution of artiodactyls within the sequence of the Geiseltal strata corroborates the biostratigraphical concept of the land mammal age Geiseltalian (Franzen & Haubold l986b) as well as the mammalian reference levels MP 11-13 (Franzen 1987). Reconstructions of the skulls and skeletons allow conclusions on the functional morphology and palaeoecology of the artiodactyls of the European Middle Eocene 

A classification should be both usable and useful,not too complex either in the amount of splitting or in the number of hierarchies involved, and not so simple as to give a false assurance of knowledge of relationships. Classifications are only possible because we do not have complete knowledge of the evolution of the organisms concerned because gaps in the record are necessary to allow the separation of the various taxa. Rodent classification is complicated by the large number of organisms involved and by the geat amount of parallelism that has taken place in the evolution of any and all features. If several independent features are characteristic of a certain taxon, should an effort be made to define the group on the basis of all the features, or should only one be selected as the determinant ? Unless the evolution of the several features was closely linked, the former solution will sooner or later lead to insurmountable problems. 

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.