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. 

Designated the type-locality of a late Eocene paleomammal zone, Robiac has recently been the object of important excavations. The first results of the new collecting, as  well as a revision of the material in old collections, are given in this work.
Two stratigraphic section, cutting through the two sites presently distinguished (Robiac-Nord and Robiac-Sud) reveal the lithologic variation at the base of the Fons Limestone and the localization of three fossiliferous beds at Robiac-Sud.
The molluscan fauna and the flora (charophytes), which have already been described, as well as that of the lower vertebrates, have been listed.
A list of 46 mammalian species (only 16 species were known previous to 1964) has been established. The micro-mammals, nearly all new in this fauna (marsupials, insectivores, bats, rodents, primates, and some smallsized artiodactyls), Were obtained only after screen-washing of the matrix; about 4 tons of sediment were thus treated.
The artiodactyls have been the most extensively analyzed; 6 genera, of which one is new, have been recognized. The latter is described as Robiacina minum n.g., n.sp., and represents a very small artiodactyl of the family Anoplotheriidae. The taxonomie status of certain species formerly described has been clarified by the designation of lectotypes (Cebochoerus robiucensis, Catodonerium robiacense, Xiphodon castrense).
The paleontologic corrélations at present possible between the late Eocene faunas have allowed the relative positions of te different French localities of this age to be established; the Guépelle locality, it seems, could define in the future a new paleomammal zone.
  

We present here a new updated counting of the perissodactyls of Robiac, the type locality of the MP 16 level of the biochronological scale of paleogene mammals and that of the Robiacian stage of Eocene Land Mammals Ages in Western Europe.
The outcrop of Robiac consists actually of two 500m apart loci, Robiac-Nord and Robiac-Sud, considered of the same age according to the current discriminating power, and is dated from -38,7 MA after the last faunal, magnetostratigraphic and climatic calibrations.
It has yielded a very abundant and rich of 21 taxa perissodactyl fauna, topped by the giant Lophiodon lautricense, last representative of the family Lophiodontidae, of which it is the last proved deposit. The Palaeotheriidae are much diversified with 5 genera and 9 species of "Pachynolophinae", 3 genera and 10 species of Palaeotheriinae. Nine taxa have been defined from Robiac: Chasmotherium depereti n. sp., Palaeotherium castrense robiacense Franzen, 1968, the genus Leptolophus Remy, 1965 with the species L. stehlini Remy, 1965 and L. magnus Remy, 1998, Anchilophus (Paranchilophus) jeanteti Remy, 2012, Metanchilophus chaubeti Remy, 2012, Lophiotherium robiacense Depéret, 1917 and Pachynolophus gaytei n. sp.
The faunal Robiac cenogram with the associated flora testify to a hot, wet and forestal environment, likely corresponding to a short warming climatic phase; the broken up fossil bones should have been carried away and then gathered in swamp areas along the banks of a meandering river.
The swarm of mammals of Robiac, the richest of contemporaneous deposits, has been followed by a drastic drop in perissodactyl diversity at the MP 17A level; a crisis which could have originated in a renewal of the global Eocene cooling. Fons 4, the type-locality of this level, is largely scarcer in perissodactyls and its cenogram testifies to a less diversified fauna, with on the whole smaller species, that likely means a cooler and drier climatic environment; a new perissodactyl diversification occurred but later.
  

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 new fauna of Collet Redon (Bouches-du-Rhône, France) is dated by three rodents: Megacricetodon aff. bavaricus, Democricetodon affinis mutilus and Peridyromys cf. hamadryas. They correlate this locality with Oggenhof and Ohningen in Bavaria (Western Germany). As the radiometric age of Ohningen is estimated between 14 and 13 M.Y., these three localities are of Serravallian age. This datation brings a complete readjusment of the stratigraphy of the section of Collet Redon formerly described by Collot and Combaluzier. The marine deposits with underly the continental formation with the mammal fauna, are Burdigalian. The angular unconformity between the marine and the continental deposits gives evidence of an episode of emersion on the margin of a sedimentary basin, with deformation and erosion. Owing to the newly discovered fauna, this geodynamical event is clearly settled within the regional geographical and chronological context. Lacustrine and continental deposits of such an age were up to now unsuspected in this area. 

Revision of the Tayassuidae from the old collections of the Quercy leads to interesting facts about taxonomic and phylogenetic problems. It could not have been well done without constant comparison with contemporaneous Tayassuidae from stratified series, as well as with European Miocene Tayassuidae and Hyotheriinae. The result is that only three species are present in the Phosphorites of Quercy: Doliochoerus quercyi FiLHOL (represented by two sub-species: the older, D. quercyi quercyi and the more recent, D. quercyi aquensis), Palaeochoerus gergorianus CROIZET et BLAINVILLE and Palaeochoerus purillus nov. sp. The two former species disappeared with Stampian time, while the third is the direct ancestor of the Aquitanian Palaeochoerus typus POMEL, which became extinct before the beginning of Burdigalian.

The comparison with Hyotheriinae brought to light new criteria for determinations, based on the study of lower premolars. These observations are condensed in a table of keys for determinations.

As a result of these studies, it came to light that the Suoidea of the Oligo-Miocene of Europe have never given rise to, except in rare cases, very long lineages. The different forms of pigs are replaced constantly in Europe by the simple game of extinctions and migrations. The reason of that discontinuity is considered here.