An interpretation of the marine reptile fossil record, based on the existing litterature and complemented by the review of ancient collections and the study of new material, permits a better understanding of Mesozoic marine ecosystems. An inventory of the marine reptiles known from the Lower Triassic to the Paleocene is presented: 46 families, about 200 genera and 400 species have been recorded. This data base includes commentaries about systematics, stratigraphical ranges and geographical distribution of taxa. Marine reptiles include a mosaic of not necessarily closely related groups: ichthyosaurs, thalattosaurs, hupehsuchians, pachypleurosaurs, placodonts, nothosaurs, plesiosaurs, pliosaurs but also crocodiles, lizards, snakes, turtles. The diversity studies reveal that the fossil record of marine reptiles has been punctuated by two mass extinctions, during the Middle-Upper Triassic transition and at the Cretaceous-Tertiary boundary. The Jurassic-Cretaceous and Cenomanian-Turonian boundaries (the latter marked by the disappearance of ichthyosaurs) are potential crisis periods, but current data are not sufficient to reach conclusions. The Ladinian-Carnian transition is characterized by the disappearance of 64 % of families and affects essentially coastal forms. This extinction coincides with an important regressive phase. During the Upper Triassic, a faunal reorganisation within marine reptiles leads to the progressive disappearance of near-shore forms and to the development of pelagic groups. During the Maastrichtian-Danian crisis, 36% of families died out. Large-sized pelagic forms such as mosasaurs and elasmosaurs were the most affected and their extinction seems to have been rather sudden. On the other hand, pliosaurs and protostegid turtles became extinct, but were already declining. The survivors were near-shore forms such as crocodiles, snakes and some turtles and they may have taken refuge in freshwater environments. A break in the food chain based on phytoplankton is proposed as an extinction scenario for pelagic forms.

  

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 present research deals with the remains of a lagomorph found at Valdemino cave and comes to the conclusion that it is a rabbit with peculiar characteristics in comparison with the other known species Oryctolagus laynensis, O. lacosti and 0. cuniculus. We studied other fossil remains of rabbit populations from Villafranchían and middle Pleistocene deposits and compared them with data from the literature and with recent material. The analysis leads us to maintain two phylogenetic hypotheses about the history of Oryctolagini. The ñrst one, already formulated by Lopez Martinez, suggests that 0. cuniculus derives from O. laynensis,while the origin of O. lacostí is unknown; according to the second hypothesis 0. laynensis would be the common ancestor of two phyletic lineages, 0. lacosti and 0. cuniculus. In both cases the lagomorph from Valdemino would be the form derived from 0. lacosti, from which however it differs in peculiar characteristics. Since the rabbit from Valdemino survives until the beginning of Postgalerian, its disappearance may coincide with the retreat of 0. cuniculus from western Europe in Spain and, perhaps, in south-western France, before the last glaciation. O. cuniculus survived in Spain, from where it spread once again over western Europe as a result of man.

  

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. 

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.
  

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 St-Dézéry local fauna (3 reptile-, 4 mammal species) is approximately of the same age as the La Débruge or the Ste-Néboule faunas. It conduces to a better dating of the limestones underlying the Célas sandstones. A large part of a mandible of Amphimeryx was found there, which documents the record of this family of small artiodactyls 

A well-preserved anterior cranium of Paranourosorex gigas RZEBIK-KOWALSKA, 1975 from Podlesice, Poland, provides additional knowledge of this rare shrew, including almost complete maxillary dentition. The systematic status of this species as a relative of recent Anourosorex MILNE-
EDWARDS, 1870 is confirmed 

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 investigations undertaken at Crivadia (Hateg Depression, Hunedoara District, Romania), the type locality of Crivadiatherium mackennai RADULESCO el al. (Radulesco, Iliesco et lliesco, 1976), led to the discovery of remains of a new Embrithopod. Close to the above mentioned species, but larger in size, this animal is here described as a new species of Crivadiatherium, C. iliescui. ln addition, the comparison made between the forms indicated above and Palaeaamasía kansui OZANSOY from the Eocene deposits of Anatolia (Ozansoy, 1966; Sen et Heintz, 1979) showed that the latter species included a heterogeneous material; this permitted us to distinguish the form in the Anatolian locality Ciçekdag-Arabin Kôyü under the name Palaeoamasia sp. The geographical distribution and diversity of the Embrithopod species under discussion (Balkan, Anatolia) support the idea of an eurasiatic origin of this group and seem to suggest the existence during the Eocene of a particular faunal province in south-eastern Europe. 

The analysis of oxygene isotope variations as well as paleobotanical data suggest that the Oligocene/Miocene boundary corresponds to a transitional period marked by floristical and climatic variations. During this period, the pyreneo-alpine tectonics has contribued to modify the geography and western Europe landscapes. Faunal changes (appearances, extinctions, migrations) are observed in different mammalian groups, notably in the rodents. A study of the evolutionary trends and patterns in paleogene rodents is involved for the period ranging from level MP 28 of the Late Oligocene to the Early Miocene, including the Oligo-Miocene boundary.
The Rodents fauna from the sites of Venelles (Bouches-du-Rhône District, France) and Thezels (Lot, France), previously mentionned in litterature, have been studied. The first description of the Eomyidae of La Milloque (MP 29) has been completed. These faunas are compared to those from various localities dating from the considered period. In La Milloque, a new representative of the Eomys species is described next to a form close to Rhodanomys hugueneyae ENGESSER, 1987. It is the Eomys milloquensis nov. sp., the likely descendant of Eomys quercyi COMTE & VIANEY-LIAUD, 1987. Two new species are also described in Thezels: Eucricetodon thezelensis nov. sp., resulting from a likely and local evolution of Eucricetodon praecursor (SCHAUB, 1925) from La Milloque, which, in the same geographic area, could be at the origin of Eucricetodon hesperius ENGESSER, 1985 from Paulhiac. Plesiosminthus admyarion nov. sp., quite distinct from Plesiosminthus schaubi VIRET, 1926, which announces Plesiosminthus myarion SCHAUB 1930. Venelles 'Plesiosminthus schaubi population is considered as a sub-species, named Plesiosminthus schaubi meridionalis nov. subsp. New phylogenetic patterns are proposed. Among the Eomyidae, a quantification of various features of the M1-2/ crown (hypsodonty, degree of abrasion, occlusal angle, state of development of the I and V anticlines), and a comparison with the occlusal diagram of the other teeth among various other populations allows a more efficient separation of Eomys and Rhodanomys genera. In Western Europe, and within this period, it finally does not seem possible to gradually connect the genus Eomys to the genus Rhodanomys. The evolution of the Eomys quercyi - milloquensis lineage seems to underline a similar evolution to that which may have led from the Eomys to the Rhodanomys form. The latter which appears totally accomplished at level MP 29 of the Oligocene is considered as an immigrant. If we compare the most representative species of the Venelles, Thezels, and Coderet sites, (i.e. Rhodanomys, Eucricetodon, Adelomyarion, Peridyromys, Plesíosminthus), it becomes impossible to confirm their biochronological separation. The noticeable differences between the populations may be interpreted as geographical variations. An explanation to these variations, and to fauna's evolution during the Late Oligocene and Early Miocene can be found in the environmental modifications, supported by isotopic, paleobotanical and sedimentologic analysis. A tentative reconstruction of the environments is attempted by the cenogram method. The analysis of the fluctuations of fauna's diversity shows variations which may be correlated to a drop in temperature at MP 29, during the Late Oligocene, followed by an increase in temperature along with an aridity phenomenom, during the basal Miocene (MN O).The confrontation of various methods give the opportunity of reconstituting and comparing the evolution of the environment of three sequences of sites chosen from different regions. Ecological affinities of various rodents' species are being examined. It is possible to consider that the integration of all the conclusions resulting from this study should lead to an explanation to the evolution of rodents for the period around the Oligocene-Miocene boundary. The site of Coderet- level 3- would be posterior to the latter, at the beginnig of the Miocene, and would mark the level MN 0 of the Aquitanian.

  

The fauna from three new rodent localities (Castelmaurou, Grépiac-carrière et Grépiac-rive gauche) from Oligo-Miocene molasses of the Toulouse area is described. The one from Colomiers is completed. 11 species belonging to 4 families (Cricetidae, Eomyidae, Gliridae, Sciuridae) are present. The Miocene localities of Grépiac-carrière and Colomiers are correlated with Balizac, La Brète, Lambert and Lespignan. Grépiac-rive gauche is just a little older than these sites. Castelmaurou is somewhat younger than La Milloque and belongs to Oligocene. 

Abstract not available 

Dichobunoid artiodactyls are described in this paper from the middle Eocene Geiseltal lignite deposits near Halle (Sachsen-Anhalt, Germany). The genera Eurodexis and Parahexacodus are established based on odontologica1 studies. The type-species are E. ceciliensis (FRANZEN & KRUMBIEGEL, 1981) and P. germanicus n. sp. from the "obere Mittelkohle" (see text), MP 13. The genera are referred to the new subfamily Eurodexeinae (Dichobunidae, Artiodactyla, Mammalia), which also contains the monospecific genus Eygalayodon SUDRE & MARANDAT, 1993. These new genera show many features similar to North American homacodontids and antiacodontids. They exemplify a high degree of diversity in European dichobunids. Moreover, the family Dichobunidae includes the Dichobuninae and the Hyperdichobuninae. The connection of the posthypocristid with the postentocristid, the shift of a medial to a lingual position of the hypoconulid on the lower molars and the development of a large, caniniform P1 are regarded as the principal tendencies of the eurodexeines. The entoconid is larger and more mesially situated compared to that of Diacodexis. The hypoconulid has a lingual position on a broad postcingulid. The elongation of the premolars and the presence of diastemata are considered associated with extension of the muzzle. This and the acute tubercles of the molars could indicate a limited degree of insectivory. Protodichobune cf. oweni and Diacodexis cf. varleli, first reported here from the "untere Unterkohle" (MP 11) of the Geiseltal, demonstrate the existence of forms in the basal part of the middle Eocene, that are direct descendants of lower Eocene ones. Eurodexis russelli n. sp. from MP 10 of Premontre is the most primitive representative of Eurodexis. A further part of this lineage could be Messelobunodon sp. from MP 11 of Messel (Germany). Another form from Premontre, referred to Eurodexeinae indet., represents the origin of the lineage to Parahexacodus germanicus n. sp. from the Geiseltal (MP 13). The identification of several lineages in MP 10 is evidence of an adaptive radiation during this time. Unfortunately the history of the earlier species of Diacodexis is not known well enough to exclude earlier diversifications. Our study shows the independent development of artiodactyls at the end of the lower Eocene in Europe, North America (and maybe in Asia) with much convergence. The question of the geographic origin of the genus Diacodexis is still open. 

Based on material from 30 localities, morphologic dental, cranial and biometric analyses have permitted the characterization of two parallel Issiodoromyine lineages, and also the definition of diverse species representing several evolutive stages. Thus it is that new lineages complete the contribution made by the Theridomyinae and Cricetidae and permit, for the Quercy in particular, additional precision in the biochronologic succession of the localities. One of the lineages is limited to the genus Pseudoltinomys LAVOCAT; the other evolves from the genus Elfomys HARTENBERGER to the genus Issiodoromys BRAVARD in GERVAIS. The latter is affected by profound anatomical changes due to a functional modification of the mastication apparatus. These changes seem to be able to be put in relation with the aridification and cooling of the climate at the end of the Eocene. At the end of the middle Oligocene, a new chewing structure is achieved. It is found in diverse living rodents that inhabit a rather arid steppe environment (Cavia, Pedetes, Ctenodactylus). To these supposed nearby ecologic conditions, these rodents have responded in a convergent fashion. It is possible to attribute to the extreme specialization of Issiodoromys its incapacity to adapt to the new climatic crisis of the end of the Oligocene. The arrival of immigrants may be considered as another cause of its disappearance at this time, complementary or not with the first. 

The murid fauna of the terminal Pliocene of southwest Europe is rich in at least eight genera and ten species. With the species belonging to the genera Apodemus, Rhagapodemus, and Stephanomys not being studied here, the study of the other murids resulted for one thing in the description of three new genera and three new species: Castillomys crusafonti n. g., n. sp., Occitanomys brailloni n. g., n. sp., Anthracomys meini n. sp., Valerymys ellenbergerí (THALER) n. g., and for another thing in the recognition of a form hitherto unknown in this region, Micromys praeminutus KRETZOI. Systematic study has shown that certain species of the terminal Pliocene fauna had their ancestors in the Turolian fauna presently known in Spain. The evolutionary lineages thereby recognized have been studied more in detail and a list of the evolutionary tendencies of the dendal characters has been given. A chart of the probable phyletic relationships between the different murids of the Pliocene faunas of southwest Europe (With the genus Rhagapodemus and Apodemus dominans being excluded) is given in conclusion of this work. 

About the early radiation of Rodents, we have now from the early tertiary of Asia, a new fossil record, and
we can do new interpretations. First the problem of the origin of Rodents is studied : considered as a sister group of Lagomorpha, it is possible to find their ancestors between the Mixodontia. Second the new facts about the origin of modern groups of Rodents are reviewed. A general scheme of this diversification can be proposed. 

We report the first confirmed fossil bats from North Dakota, including a new species referable to the Vespertilionidae represented by a maxilla with P4-M3 from the Brule Formation, Fitterer Ranch local fauna, early Oligocene, Whitneyan North American Land Mammal Age. Unassociated postcranial fragments of the humerus and femur also represent a vespertilionoid, but appear to reflect a different, unidentified species. The new taxon, Quinetia frigidaria sp. nov., is referred to the genus Quinetia, previously known only from approximately contemporaneous deposits in Europe. The new species is larger than Quinetia misonnei from the early Oligocene of Belgium. It is similar in some morphological characters to Chadronycteris rabenae (Chiroptera incertae sedis) of the late Eocene (Chadronian) of northwestern Nebraska and to Stehlinia species (?Palaeochiropterygidae) from the Eocene and Oligocene of Europe, but differs from each in morphological details of the dentition and maxilla. An unassociated talonid of a lower molar from Fitterer Ranch shows myotodont morphology, unlike the nyctalodont lower molars in Q. misonnei, and thus represents a second chiropteran taxon in the fauna. Quinetia frigidaria is a member of a Paleogene radiation of bats near the low point of the Eocene-early Oligocene decline in global temperatures, increased seasonal aridity, and loss of tropical floras from mid-latitude North America. 

A reconstruction of a multituberculate endocranial cast is made on the basis of a complete natural cast prepared from the skull of Chulsanbaatar vulgaris, and other less complete endocasts, all from the Late Cretaceous of Mongolia. The multituberculate endocast is of mammalian pattern but it has retained a therapsid-like lateral profile with a deep rhombencephalon and a shallow telencephalon. It is characterized by: a heart-shaped cross-section of the telencephalon; an extensive lissencephalic neocortex; a very prominent pons placed far anteriorly; a lack of cerebellar hemispheres, and very large paraflocculi. Its structure, very different from the brains of other mammals, suggests thats the Multituberculata branched very early from the main mammalian stock. This supports Simpson's (1945) idea that the Multituberculata should be placed in a subclass of their own: Allotheria MARSH. The endocast and braincase structure show that the Multituberculata had strongly developed senses of smell and hearing. The encephalization quotient of approx. 0.55 evaluated for Ch. vulgaris is relatively high for a Mesozoic mammal. 

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.