Three erinaceomorph species are known from the early Middle Eocene of Grube Messel near Darmstadt, Germany, which are referred to the family Amphilemuridae. Pholidocercus hassiacus, Macrocranion tupaiodon, and Macrocranion tenerum showed extraordinary adaptations to their different life strategies, and several of their specializations are unknown among living insectivores. Pholídocercus was a well-defended robust animal with an opportunistic feeding strategy. Macrocraníon zupaiodon was a slender forest floor-dweller with saltatorial specializations to escape from predators; fishes were the preferred component of its omnivorous diet. Macrocranion tenerum exhibited a combination of both survival strategies, extremely elongated hind limbs for rapid and even ricochetal flight and a spiny exterior as an effective protective device; it was probably specialized for feeding on ants. Thus, closely related, omnivorous-insectivorous forest floor-dwellers could exploit the Messel ecosystem. 

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.

  

The formic acid preparation of a nodule collected from the Lower Triassic of Spitsbergen, and containing a skull with some associated postcranial elements of Lyrocephaliscus euri (WIMAN), precises and enriches previous descriptions of the reputedly well-known trematosaur. lt permits more detailed descriptions of the occipital region, of the course of the carotid arteries and collateral vessels, and refutes the previous description of a stapedial foramen in trematosaurs. The discovery of pleurocentres associated with the other vertebral components confirms the primitive rhachitomy of trematosaurs. 

The entelodonts of the Quercy phosphorites are essentially known from isolated teeth. The skull remains attributed to Entelodon magnum by Kowalewsky in 1876 and the type left mandible of Enteladon depereti RÉPELIN, 1918 do not belong to this family. From a morphologic point of view, the teeth from Quercy are quite comparable to those from the type localities of E. magnum and E. deguilhemi. In the absence of distinctive anatomical criteria between E. magnum (small species from the level of Ronzon) and E. deguilhemi (large species from the level of Villebramar) they are referred, according to their size, to one or the other of these two species. However, some of them are intermediate in size. Their existence speaks in favor of a close relationship between E. magnum and E. deguilhemi and confers a real stratigraphic interest to these entelodonts of Western Europe. Finally, some anatomical characters (notch on the mesial border of P4, presence of a paraconid joined to the metaconid, trigonid higher than talonid) considered until now as peculiar to the North American Archaeotherium and not yet cited in its European contemporary Entelodon have been brought to light on the teeth from Quercy.

  

The locality of St.-Victor-la-Coste (Gard) has yielded, rather abundantly, teeth of two glirids hitherto very poorly known: Glirudinus praemurinus (Freudenberg) and Glirudinus glirulus (DEHM). It has permitted, moreover, new views on the evolution of Peridyromys murinus (POMEL). Study of these forms confirms the late Oligocene age of the fauna, without allowing, however, further precision. 

Stratigraphic studies in the Aktau Mountains bordering the Dzhungarian Alatau Range in southeastern Kazakhstan have included mapping of Tertiary lithostratigraphic units, documentation of fossiliferous deposits, correlation of sections, etc. These investigations have led in turn to revised interpretation of the Tertiary geology of the area. The Tertiary sequence in the Aktau Mountains is represented by three lithostratigraphic units (in ascending order): (1) the middle Eocene Akbulak Formation; (2) the Oligocene Aktau Formation with a lower member including white quartz sands that contain fossil mammals, and an upper member including red-colored clays and sandstones, brick red clays, an anhydrite and gypsum clayey horizon, and bright brown-red clays; and (3) the upper Oligocene-Miocene Chul'adyr Formation with a lower member of greenish and yellowish conglomerates and gritstones, a middle member including grayish and yellowish sands and gritstones, and an upper member including brown and red clays and carbonate- and anhydrite-rich clays. The Aktau and Chul”adyr Formations represent separate cycles of sedimentation. Mammalian biostratigraphy and biochronology of the three vertebrate faunas in Aktau Mountains are reviewed. The mammalian fauna from white sands of the lower Aktau Formation is small but includes Ardynia and is thought to be early Oligocene in age. The mammalian fauna from conglomerates and gritstones of the lower member of the Chul”adyr Formation is also small but includes Paraceratherium and is thought to be late Oligocene in age. The mammalian fauna from sands of the middle member of the Chul'adyr Formation is extensive, with micro- and macrofauna attributed to Neogene mammal zones MN4 to MN 6, indicating a latest early Miocene to earliest middle Miocene age (Orleanian-Astaracian). Most genera of middle Chul”adyr mammals are known from the middle Miocene Shanwang faunas of China and from the Castelnau-d”Arbieu faunal assemblage (MN4-MN6) of southwestern France. 

The scientific career of D.E. Russell began with a Pliocene fauna from Oregon, and then turned in the direction of European Paleogene mammals. Field work followed by study of the mammals that were collected, firstly in the Paleocene and later in the early Eocene, greatly rejuvenated learning in this field. Syntheses on the Northwest European Tertiary basin and on European marnmals and stratigraphy came next. Research on the Eocene of Asia was carried out jointly with Gingerich on Pakistan and with Dashzeveg on the faunas of Mongolia. An important synthesis on the entire Paleogene of Asia, joint with Zhai, followed. Field work in Africa with Sigogneau-Russell led to the discovery of Mesozoic mammals there. A synthesis of mammalian paleofaunas of the world was written with Savage, and a similar synthesis of Cenozoic vertebrate faunas is currently being prepared. These achievements reflect the perennial importance of field work, numerous collaborations with both amateurs and professionals, and the human qualities of this author.
  

Amongst a collection of selachian teeth made at Hoegaarden in a marine level of Bruxellian (Lutetian) age, containing a reworked Landenian (Sparnacian) fauna mixed with a contemporaneous one, a few teeth of  terrestrial mammals have been discovered. They comprise two rare European taxa: ? Hallensia sp. and Palaeonictis gigantea, both known from the Landenian. Even though the ?Hallensia has not been definitely identified, il differs from the only perissodactyl of this age previously recorded from Belgium (Cymbalophus cuniculus). 

The earliest North American rodents occur in basal Clarkforkian beds of the Fort Union Formation at Big Multi Quarry near Bitter Creek, northern Washakie Basin, Sweetwater County, Wyoming, and in closely correlative Fort Union beds formerly accessible in the Eagle Coal Mine near Bear Creek, northern Clark's Fork Basin, Carbon County, Montana. Two new species of early Clarkforkian rodents, Paramys adamus and Alagomys russelli, are described from Big Multi Quarry. Paramys adamus is represented by virtually complete upper and lower dentitions, which demonstrate that this species is one of the most primitive North American paramyids yet discovered. These specimens form the basis for a reevaluation of the content and stratigraphic range of P. atavus, which is known with certainty only from Bear Creek. Alagomys russelli is the first North American record for the enigmatic rodent family Alagomyidae, otherwise known from ?late Paleocene-early Eocene localities in Mongolia and China. Phylogenetic analysis of dental and gnathic traits suggests that Alagomyidae form the sister group of all other undoubted rodents. At least two rodent clades, alagomyids and basal paramyids, seem to have invaded North America from Asia at the beginning of Clarkforkian time, but only the paramyids persisted to undergo a significant evolutionary radiation in North America. 

The Paleogene faunal assemblage from Antofagasta de la Sierra (Catamarca, Argentina), is here presented, both in its geological and systematic aspects. The fossil bearing levels are referred to the Geste Formation (Pastos Grandes "Group"). The described specimens belong to the Classes Reptilia (Orders Crocodylia, Serpentes and Chelonii) and Mammalia (three taxa from the Superorder Marsupialia, representatives of the Orders Edentata, Condylarthra, Pyrotheria and Astrapotheria, and six families of the Order Notoungulata). This fauna is referred to the Mustersan Age, which in Patagonia represents the Middle Eocene. Such chronologic assignment is based on the presence of characteristic taxa, their evolutionary stage and on stratigraphic evidence. Finally, a brief comparison with other faunal assemblages from the Early Tertiary of Argentina and Chile, is presented. 

A detailed comparative study of a complete skeleton of Bachitherium and a cladistic analysis of the sub-order Neoselenodontia lead us to propose a cladogram and a new classification of this group. The Tylopoda are the sister-group of the Ruminantia, which are chiefly defined by the fusion of the cuboid and navicular. Within this infra-order, Amphimeryx is the sister genus of a tetraselenodont group, in which the Hypertragulidae are well-separated group from a monophyletic group defined by the loss of trapezium, fusion of capitatum and trapezoid, and the isolation of the hypoconid on lower molars. The most primitive genera of this group, Lophiomeryx and Iberomeryx still have an open trigonid on the lower molars, but this is lingually closed in Archaeomeryx, sister-genus of the higher Ruminantia which have fused metatarsals and more evolved milk teeth. We divide them into two pan/orders : Tragulina (including the recent and miocene Tragulidae, and the North-American Leptomerycidae), and Pecora, with reduced lateral metacarpals and a new crest (telocristid) on the lower premolars. Within the Pecora, the upper molars of Gelocus are more primitive than those of Bachitherium (a genus with many autapomorphies in the dentition) itself more primitive than the group Prodremotherium + Eupecora, with fused metacarpals. We consider the Eupecora (including several genera without frontal appendages) to be monophyletic. 

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.

  

Deux types de remaniements post mortem me paraissent caractéristiques de l'état de conservation des dents de mammifères fossiles dans les Phosphorites du Quercy :

1) Des destructions localisées d'origine biologique, sous forme de galeries de morphologie très variable creusées dans la dentine et le cément, et impliquant sans doute la participation de différents types de micro-organismes. Ces altérations se sont développées peu de temps après la mort, avant la fossilísation proprement dite et se sont rapidement arrêtées après l'enfouissement dans le sédiment phosphaté.

2) Des perturbations dans les structures de la dentine liées aux variations locales de minéralisation, provoquées par une imprégnation diffuse des zones les moins calcifiées par divers minéraux et probablement surtout de l`apatite. 

The exploitation of new early Eocene localities in the Paris Basin has resulted in the collecting of  numerous mammalian remains, among which are about 300 isolated teeth representing the rodents. They belong, for the most part, to the paramyid group. Only the latest level of the early Eocene has yielded rodents belonging to the pseudosciurid group. The paramyids, the object of this study, are represented by at least 5 genera and 10 species; they are distributed among 4 clearly dilferentiated subfamilies : Paramyinae Simpson 1945, Pseudoparamyinae Michaux 1964, Ailuraviínae n. subf., Microparamyinae Wood1962.
It results from this study that the principal types of rodents in the middle and late Eocene of Europe are clearly related to the forms described here: Plesiarctomys Bravard 1850 is related to Pseudoparamys Michaux 1964, Ailuravus Rütimeyer1891 to Meldimys n. gen., Gliravus hammeli Thaler 1966 to Microparamys nanus (Theilard1927), and some Masillamys Tobien 1954 to Microparamys russelli Michaux 1964 and to M. sp. 1. Gliravus and Masillamys are the oldest representatives of the Gliridae and the Pseudosciurídae, respectively, families which will progressively replace the Paramyidae in the course of the middle and late Eocene.
Two stages can be recognized in the history of te European Paramyidae fauna during the course of the early Eocene: the older is characterized by the Mutigny fauna, the younger by the Cuis fauna.
The Mutigny fauna appears already rather diversified and does not completely correspond, point by point, to the homologous fauna of North America. A geographic differentiation seems to have been manifested rapidly, unless the fauna established in Europe was already a little different from that which established itself in North America. 

The re-examination of six fossil selachian species has involved the creation of six new genera: Squatiscyllium, Protolamna, Parotodus, Abdounia, Physogaleus, Hypolophodon and of one new species : Prozolamna sokolovi. The modification of the generic statute of these species allows to clarify their systematic position and to define their relationships at a familial level. 

The description of original material of anthracothere and proboscidean in the new locality of Bir el Ater 3 from East Algeria, and a thorough review of early Libycosaurus remains of Bir el Ater 2 allows us validating L. algeriensis as the smallest and earliest species of Libycosaurus and probably the earliest migrant of the genus from Asia. The presence of a Tetralophodon in the Neogene Nementcha formation might represent the earliest occurrence of the genus in Africa. These original fossil remains allow us to discuss the age of the Neogene part of the Nementcha formation close to the Serravalian/Tortonian boundary. 

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 late Pliocene site (MN 16) of Balaruc II (Hérault, France) has provided remains of the following amphibians and reptiles: Chelotriton pliocenicus nov. sp. and Triturus marmoratus (Salamandridae), cf. Rana (Ranidae), cf. Blanus (Amphisbaenidae), cf. Agama (Agamidae),  Gekkonidae indet., Lacerta s.l. (Lacertidae), "Ophisaurus" sp. (Anguidae), Michauxophis occitanus (Aniliidae), Erycinae indet. (Boidae), Elaphe cf. E. longissima and Malpolon sp. (Colubridae), cf. Naja (Elapidae) and Vipera sp. (Viperidae). The salamandrid Chelotriton pliocenicus and the aniliid Michauxophis occitanus constitute, up to now, the only records of these groups in the European Pliocene. The fauna is indicative of a warm, dry
subtropical climate. 

The Middle Eocene Fossillägerstätte of the Geiseltal lignite beds near Halle/S. (German Democratic Republic) is the reference locality of the European land mammal age Geiseltalian and of the Mammalian Paleogene reference levels MP 11 - MP 13. Due to this importance a reinvestigation is given of the lithostratigraphical development of the Geiseltal beds and of their vertebrate sites. The last are genetically related to the southwest border of the Geiseltal depression and the influx of carbonate-rich waters. The geographical distribution and stratigraphical position of the fossiliferous sites depends on subrosive and tectonically controlled distribution of coal seams. The geological factors and the known stratigraphical guide of some mammalian species suggest corrections of the age of some sites. Four of the alltogether five coal bearing phases contain the 35 sites with mammalian remains. By the distribution of the around 69 mammal species are characterized, with 5 faunal steps ranging from MP 11 to MP 14 or over the Geiseltalian up to the Lower Robiacian. Well distant are the faunas of MP 11 and MP 12. Beginning with MP 12 up to MP 13/14, the fossil record is very frequent by 27 sites. This evidence coincides somewhat more with the concept of land mammal ages compared to that of the punctual mammalian reference levels. 

Abundant crocodilian fossil remains have been collected, mainly by R. Lavocat. from several levels of the
Palaeogene of the Tilemsi valley (eastern Mali). Several dyrosaurids occur in the Palaeocene (Montian ?) : Phosphatosaurus sp., Hyposaurus bequaerti (Dollo). H. wilsoni (Swinton). H. nopesai (Swinton), Rhabdognathus rarus Swinton, R. compressus n. sp. ln the lower Eocene has been found a dyrosaurid which cannot be accurutely determined.In the middle Eocene were found a dyrosaurid, Tilemsisuchus lavocati n. g., n. sp., and an indeterminate eusuchian.