A cheek tooth recently unearthed in the Lopar Sandstone unit, of late Eocene age, in the northern part of Rab Island, Croatia, is one of the very few Eocene mammalian remains found in the Adriatic area. Thorough comparison of this tooth with those of Old-World Palaeogene mammalian orders suggests that it is a M3 belonging to an embrithopod afrothere. The specimen is referred to as Palaeoamasia sp. This genus was formerly known only in Eocene deposits of Anatolia but with close relatives in Romania among Palaeoamasiinae. The geographical distribution of this subfamily perfectly matches the recently-named Balkanatolian landmass, which experienced in-situ evolution of endemic mammals prior to the Grande Coupure event that occurred around the Eocene–Oligocene transition. This last event is characterised by massive Asian immigration in Western Europe and the supposed extinction of many endemic Central and Western European mammals, including Palaeoamasiinae.
  

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 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 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. 

A rear skull from the Quercy Phosphorites is described. It documents a new perissodactyl genus, likely assignable to the family Palaeotheriidae and probably paleogene of age. Owing to the lack of any tooth, this family assignment remains however somewhat hypothetical. The specimen is firstly characterised by the presence of a wide epitympanic sinus swelling and hollowing the squamosal shell and the post-glenoid process. This cavity might make up a peculiar pattern of improvement for the hearing apparatus by carrying out a kind of drum near the middle ear, whereas the bony tympanic remains barely bulged and forms but a few developed auditory bulla. This pattern appears an outcome of a trend observed with many palaeotheriids, such as Plagiolophus. Furthermore, the endocranial cast shows a rather high degree of gyrencephaly for a paleogene mammal. The prominent lambdoidal crest points out a powerful nape musculature and a lowered head bearing. Consequently, it is assumed that such an animal was probably living in somewhat open places, at the expense of rather tough vegetables. It might have been accordingly provided with a semi-hypsodont, cement covered, "plagiolophoid" dentition. 

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. 

The tooth morphology of the Thalattosuchia (marine crocodilians from the Jurassic and the Early Cretaceous) is analysed. The Callovian from Poitou and the Kimmeridgian from Quercy have yielded many remains of Metriorhynchus, Steneosaurus and Machimosaurus. These remains allow us to study the variations of tooth morphology during ontogenic growth, tooth replacement and the location of the teeth. We have defined different tooth types for these genera. In Metriorhynchus, the two tooth types defined do not coincide with the two groups recognized in the Callovian (broad-skulled and narrow-skulled metriorhynchids) but reflect the prey preferences of these forms. In Steneosaurus and Machimosaurus the five tooth types deñned are in agreement with the main taxa known from the Bathonian to the Early Cretaceous. This study allows to precise the function and the prey preference of the Thalattosuchia during the Jurassic and the Early Cretaceous.

  

A new European rodent from the middle Eocene of Spain, Zamoramys extraneus n. gen., n. sp., appears to be closely related to the middle Eocene chapattimyid rodents of Indo-Pakistan. This contradicts the generally accepted paleobiogeographic hypothesis of a Tethyian barrier between Europe and Asia isolating Europe during the middle Eocene. Because of this barrier, some authors have proposed that European and Asian rodents were not closely related, their similarity being the result of morphological convergence. Here monophyly has been tested, using the parsimony criterion, based on an analysis of dental characters (including discussing of homology and the validity of some characteristics). Our results indicate a phylogenetic relationship among the Asiatic Ctenodactyloidea, Zamoramys from Spain, and the European endemic Theridomyoidea. We also conclude from our analysis that theridomyoids and European ischyromyoids are probably not closely related phylogenetically. 

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. 

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. 

The Palaeobatrachidae until now have not been reported from France. The present note makes known the discovery of very significant remains in three Tertiary localities of France: Cernay (late Paleocene), Laugnac (late Aquitanian) and Sansan (middle Helvetian). The osteologic characters, as well as the geographic and stratigraphic distribution of the family are re-stated with added details. The Palaeobatrachidae are a European family known from the late Jurassic of Catalonia (publication in course by J. Seiffert) to the Plio-Pleistocene (pre-Mindel) of Poland and Rumania. By their way of life and certain osteologic characters they are similar to the Pipidae, but they are distinguished by profound differences. It would be rash to include them in the Pipoidea or even in the Aglossa. They are apparently an independant group, essentially holarctic, which held in Europe a role equivalent to that played by the Pipidae south of Tethys. 

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. 

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. 

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.

  

A new Propalaeotherium species, clearly distinct from the genus Eurohippus, is described. It is characterized by having a similar size as P. voigti from the German Geiseltal localities (MP 11 to MP 13 reference-level), but differs in several features suggesting a slighty more derived morphology. It presents indeed less brachyodont crowns with less prominent and less elevated cingula, slightly larger relative surface of premolars, and a more marked metaconid splitting on cheek teeth. This new species is unknown from other European localities except the nearby Saint-Martin de Londres locality which has been considered older than the MP 13 level. 

The two species of Sandgrouse from Quercy, Pterocles validus MILNE-EDWARDS and P. larvatus MILNE-EDWARDS, are ascribed to the genus Archaeoganga MOURER-CI-IAUVIRÉ which includes a third, very large species, A. pinguis. The sandgrouse of Saint-Gérand-le-Puy, Pterocles sepultus MILNE-EDWARDS, is ascribed to a new genus, Lepzoganga. This form appears in the Upper Oligocene of Quercy, in Pech Desse and Pech du Fraysse localities, and is still present in the Lower Miocene of Saint-Gérand-le-Puy and Paulhiac. Recent sandgrouse live in semidesert or desert areas. The indications provided by mammal and bird faunas in the localities where sandgrouse were found, confirm that the paleoenvironment was open and arid. The morphological study of these fossils indicates that, in the Upper Eocene, the Pteroclidae were already completely individualized with respect to Charadriiformes.
  

The locality of Dams (Quercy, southwestern France) has yielded two fossil assemblages, one from the late Eocene and another from the early Oligocene, making it one of the few localities with infillings across the Eocene-Oligocene transition. At least 24 taxa (13 mammals, 11 snakes) have been identified in this locality. Study of the lissamphibian remains from Dams yields an Eocene and an Oligocene assemblage, with a total of eight taxa. The Eocene assemblage includes two unnamed salamandrine species, one unnamed pelobatid species and one pyxicephalid species (Thaumastosaurus). The Oligocene assemblage includes two unnamed pleurodeline species, one salamandrine species (Salamandra sansaniensis) and an unnamed pelobatid species. Among the eight taxa from Dams, one Eocene salamandrine and one Oligocene pleurodeline are identified for the first time in the Quercy. A review of the lissamphibians from the Quercy area identifies eleven taxa for the Late Eocene (MP19) and eight taxa for Early Oligocene (MP22), with a major turnover at the Eocene-Oligocene transition. This turnover occurs in a time of major climatic changes, with a significant decrease in temperature and precipitation and concurrent increase in seasonality in Europe, likely affecting specialized taxa.
  

Le Mémoire Extraordinaire 1988 de PALAEOVERTEBRATA regroupe dix articles consacrés au gisement à mammifères du Miocène supérieur de Montredon (Hérault), connu et classique depuis la fin du siècle dernier, et auquel est lié le nom du savant paléontologue lyonnais Charles Depéret.
Cette monographie vient normalement à la suite de celle parue en 1982 dans PALAEOVERTEBRATA, dont les différents articles traitaient de la stratigraphie du gisement, et faisaient l'étude des différents groupes de micromammifères représentés dans la faune (insectivores, chiroptères, rongeurs). 

The mammalian fauna of the Tagai locality of Olhon Island in Lake Baikal contains six artiodactyls:
Amphitragulus boulangeri, Lagomeryx parvulus, Stephanocemas sp., Palaeomeryx kaupi, Orygotherium aff. escheri, and Brachyodus intermedius. They are reported from Eastern Siberia for the first time. A description of teeth and limb-bones are given. An analysis of the systematic composition of the Tagai fauna allows it to be correlated with European faunas of the second part of the Early Miocene (Orleanian, MN 3-4) and permit suggestion of the existance of a united European-Siberian zoogeographical sub-area in the middle latitudes of Eurasia at that time. 

This paper provides a revision of the early and middle Eocene European rodents previously referred to as Ischyromyoidea, including taxa considered to be at the origin of the Theridomorpha. The use of an accurate dental terminology and a better understanding of the size and shape of their infra-orbital foramen (i.o.f.) led us to a substantial revision of this group, which allowed to better characterize them and to appreciate their variability. On these bases, phylogenetic analyses (cladistic and standard Bayesian
approaches) of early Ypresian to late Priabonian European rodent species were undertaken in order to highlight the root of the early Theridomorpha and its content. In this paper, the phylogeny was established based on 343 characters (338 dental) through 45 early Paleogene taxa using both cladistic and bayesian analyses. The ingroup included on one hand a few North American genera (Reithroparamys, Microparamys, and Acritoparamys) and European ones (Eogliravus, Ailuravus, Corbarimys, Meldimys, Euromys, Plesiarctomys, and Pseudoparamys) considered until now as being related with the North American superfamily Ischyromyoidea. On the other hand, it included genera close to the root of the Theridomorpha (Sparnacomys, Pantrogna, and Hartenbergeromys) and early Theridomyoidea (Masillamys, Protadelomys, and some Pseudosciuridae). The phylogenetic results obtained via the two
distinct reconstruction approaches are consistent in virtually all relationships. The proposed systematics here derives from these phylogenetic results. This phylogenetic context led us to change the suprafamilial, familial, subfamilial or generic attribution of several species. Characters of Theridomorpha, like the obliquely developed postprotocristid allied with the occurrence of a metalophulid I, have been found in genera previously considered as Ischyromyidae (Pseudoparamys, Euromys, Sparnacomys, Meldimys, Pantrogna, and Hartenbergeromys) as well as the large i.o.f., when preserved (Pseudoparamys, Hartenbergeromys, and Masillamys). Based on these morphological observations and new phylogenetic considerations, the content of the Theridomorpha clade is here enlarged, thereby extending back the first theridomorph radiations to the early Eocene. Aside, a new taxon (Reinomys rhomboides gen and sp. nov.) is described from Avenay. In addition, a new genus, Auroremys, is created for the species subita (Comte et al., 2012) from Chery-Chartreuve.