A recent campaign of excavations (1965-68) undertaken by the Laboratoire de Paléontologie of Montpellier in pockets of the Quercy phosphorites, has permitted the dating of several localities thanks to the analysis of their micromammalian fauna.
The rodents of localities belonging to the middle Oligocene (La Sauvetat zone) are the object of this study. This rodent fauna has been compared to the forms coming from three stratified localities belonging to the biochronologic zone of La Sauvetat :  Balm, Montalban and Lovagny.
The abundance of material, notably of theridomyids and cricetids, permitted a summary statistical study to be effected and gave some precise details on the variability of the species (Theridomys varians in particular). Other details were provided on certain groups, notably on the upper teeth of Scíuromys cayluxi and on the milk teeth of theridomyids. Some specimens of «Sciurus» sp. and of Plesispermophilus angustidens were collected. By this means, it has been possible to establish, for the first time, a precise upper limit to the epoch of their appearance in Europe. 

Seventeen species of cricetid rodent are recognized and described from lower and middle Siwalik deposits in the Potwar Plateau of Pakistan. These species are grouped in three categories, characterized as subfamilies (e. g., Megacricetodontinae, Myocricetodontinae, and Dendromurinae); an additional and more abundant category of rodents from these deposits, the Democricetodontinae, is excluded from this study, and will be described in a later study. Fifteen of the species are new, and four new genera are described. The Siwalik cricetid taxa are : Megacricetodon aquilari, n. sp.; Megacricetodon sivalensis, n. sp.; Megacricetodon daamsi, n. sp.; Megacricetodon mythikos, n. sp.; Punjabemys downsi, n. gen. & n. sp.; Punjabemys leptos, n. gen. & n. sp.; Punjabemys mikros, n. gen. & n. sp.; Myocricetodon sivalensis, n. sp.;  Myocricetodon sp.; Dakkamyoides lavocati, n. gen. & n. sp.; Dakkamyoides perplexus, n. gen. & n. sp.; Dakkamys asiaticus, n. sp.; Dakkamys barryi, n. sp.; Dakkamys sp.; Paradakkamys chinjiensis, n. gen. & n. sp.; Potwarmus primitivus, n. gen.; and Potwarmus minimus, n. gen. & n. sp. This diverse record of middle Miocene small mammals illuminates a profound radiation of cricetid rodents in southem Asia, the effects of which were felt in Europe and Africa as well as the rest of Asia. 

Pour la première fois un spécimen de lagomorphe a été récolté en Quercy. L'intérêt de ce fossile tient surtout à son âge géologique inattendu, qui recule considérablement la date de première apparition en Europe de cet ordre de mammifère, Ceci nous paraît justifier une nouvelle réflexion sur la « grande coupure» oligocène, 

Abstract: Paleontological exploration in the Turkana Basin near Ileret, Kenya yielded the most complete adult elephant cranium (KNM-ER 63642) known from the late Miocene to mid-Pliocene. KNM-ER 63642 derives from the lower Lonyumun Mb. of the Koobi Fora Fm. and dates to the early Pliocene, >4.3 Ma. The cranium is immense in size and preserves most of its structures including left and right M2-3, permitting its comprehensive comparative study and secure taxonomic assignment to Loxodonta adaurora. Features distinctive of the species and exhibited by KNM-ER 63642 include very elongate, divergent tusk alveoli, a short, biconvex cranial roof, anterosuperior angulation of the occipital planum, non-inflated occipital planum and absence of supralateral parietal "bossing," broad, flat premaxillary nasal processes, broad, laterally downturned nasal aperture superior to the level of the orbits, and M3s with wide, subhypsodont plates that are parallel-faced and separated by U-shaped transverse valleys. The M3s also exhibit characteristic L. adaurora traits of greatest width at their bases, rounded cross-sectional shape, thick enamel, abundant cementum, and strong anterior and posterior accessory conules. Of extant taxa, KNM-ER 63642 most closely resembles crania of African elephants. Its inclusion in the Loxodonta clade is tenuous, however, because shared features are either symplesiomorphic or are difficult to test for synapomorphy due to the poor fossil record of crania of late Miocene-early Pliocene elephants. Overall, the cranial morphology of KNM-ER 63642 is unexpectedly advanced for an elephant of its antiquity. Its anteroposterior compression and height are concordant with efficient proal masticatory action, indicating that by the early Pliocene L. adaurora evolved craniodental adaptations in phase with feeding preference for C4 grasses. The advantage of synchrony of morphology and behavior is reflected by the dominance of the species in the greater Turkana Basin during that interval.
  

Many types of insectivores have been described from specimens found in the Quercy phosphorites. These remains very often were not dated because they came from old collections. Recent excavations have permitted the situation of Amphidozotherium cayluxi FILHOL in the late Eocene. Two new genera are descrlbed based on material both from the old collections (Cryplotopos nov. g.) and from that recently recovered (Darbonetus nov. g., beginning of the middle Oligocene). Their systematic positions are revised and comparisons with American faunas are made. Amphidozotherium is not a talpid, but an erinaceoid belonging to an indeterminate family. Saturninia gracilis STHELIN is classified among the Nyctitheriinae, Myxomygale antiqua FILHOL among the Urotrichini Talpinae, and the genus Geotypus POMEL among the Scaptonichini Talpinae. A new study of the talpids from Auvergne has been rendered necessary. During the late Eocene and Oligocene precise morphology relationships existed between certain insectivores of Europe and North America. 

Of the ten cricetid species from the Oligocene of Western Europe, attributed until now to the genus Eucricetodon, only four prove to be utilizable - E. atavus, E. huberi, E. praecursor, E. collatum - to which it is possible to add two forms newly described: E. huerzeleri and E. quercyi. The evolullon of the genus Pseudocricetodon is also the subject of new observations. The study of the dental morphology allows us to distinguish in these two genera three lineages beginning in the middle Oligocene:

- Lineage P. montalbenensis-P. thaleri (from Montalban to Goderet), of small size, without
increase in size.
- LineageE. atavus-E. infralactorensis (from Hoogbulsel to Estrepouy), of middle size, with a regular increase in size.
- Lineage E. huerzeleri-E. haslachense (level of Montalban to that of Estrepouy), of large size, with an increase in size.

Two other forms are equally represented in these loealitles: Heterocricetodon aff. helbengi and Melissiodon quercyi. It has been possible to attribute a precise age (zone of "Cournon") to the last species, which has been defined by Schaub (l925) from material in the Old Quercy collections. The genera Pseudocricetodon, Eucricetodon, ? "Cricetodon", Leydimys, Eumys, differentiated at the beginning of the middle Oligocene in Europe, Asia and North America, seem to derive from a common ancestral group. The place of origin of this group could be situated in Asia. 

A new genus, Eppsillycteris, is erected for Adapisorex? allglicus COOPER, 1932, from the earliest Eocene Blackheath Beds of Abbey Wood, London, England. Various derived character states indicate that it belongs to the order Chiroptera (bats) rather than to the extinct "insectivore" family Adapisoricidae. Other derived character states are shared with fossil and modern members of the family Emballonuridae. Placement of the new genus in this family extends the record of the Emballonuridae back in time by about 10 million years. It is the earliest record of a modern bat family and one of the earliest bats. This implies that the differentiation of at least some modern bat families took place in the Palaeocene, where no authenticated records of bats yet exist. The primitive characters of the earliest bats make the family Nyctitheriidae an unlikely stem group for the order Chiroptera. A tentative plausible alternative exists in some unnamed upper molars from the Palaeocene of Walbeck, Germany. Wyollycteris chalix, described as a bat from the Late Palaeocene of Wyoming, U,S.A., fits better in the family Nyctitheriidae. 

Revision of the hipparion material from Montredon, including newly excavated and other unpublished specimens brings evidence of specific heterogeneity.
A fragmentary very small MC III seems very close to H. macedonicum from the upper Vallesian of Ravin de la Pluie, Greece. In that same site was also found a large hipparion.
Most of the Montredon material is referred to H. depereti. This species associates characters usually found in Vallesian hipparions (highly plicated upper cheek teeth, deep vestíbular grooves on the lower cheek teeth, robust metapodials) with characters more frequent in Turolian forms (middle size, lack of confluence in the upper premolar fossettes, lack of ectostylids on the adult lower cheek teeth, well developped keel on the MC III, facette for the 2nd cuneiform present on all MT III). H. depereti shares some of these characters with the Spanish and Portuguese hipparions transítional between the Vallesian and the Turolian (Masia del Barbo, Azambujeira) but is not identícal to any of them. The upper Vallesian hipparion material from Diavata, Greece, probably belongs to H. depereti but not the large hipparion rests from Ravin de la Pluie.
Thus, Montredon and Ravin de la Pluie may well share the same small species, H. macedonicum, but they differ in the associated one: middle-sized H. depereti at Montredon, large-sized H. primigenium at Ravin de la Pluie. Both sites, however, give evidence of small hipparions during the Vallesian, coexisting with other larger species.
The present paper also proposes an adaptation of the Kiesewalter's indices that calculates the height at the withers using the metapodial length, and discusses indices proposed by Gromova and by Sen et al. to express the relative development of the metapodial keel. 

Re-evaluation of the small collection of mammal fossils from the Changxindian Formation near Beijing, China indicates the following taxa are present: Eutheria, Hypsimilus beifingensis, cf. Miacis sp., Anthracotheriidae and Forstercooperia grandis. The presence of Forstercooperia grandis indicates an Irdinmanhan age and does not support previous assignment of a Sharamurunian age to the Changxindian Formation. 

Le présent volume traite des lagomorphes, carnivores, artiodactyles, périssodactyles et proboscidiens de la faune de Montredon (Hérault). Il clôt la monographie de ce célèbre gisement d'âge miocène supérieur du Languedoc, dont la première partie, relative aux rongeurs, insectivores et chiroptères, fut publiée en 1982.
[...] 

A short review of the genera and species of snakes from the Quercy's phosphorites described by former authors is followed by the study of specimens recently collected. Most of these latter specimens belong to the Aniliidae, Boidae, Colubridae and to the Scolecophidia; the precise systematic position of some of them is not defined yet. The following genera and species are described: Eonilius europae nov. gen. and nov. sp., Platyspondylia lepta nov. gen. and nov. sp., Coluber cadurci nov. sp. and Dunnophis cadurcensis nov.  sp.; a species described by de Rochebrune (Palaeopython filholi) is revised. One of the most important conclusions of this study is that the Colubridae appear as early as the Upper Eocene. The stratigraphic repartition of these snakes shows that the rich Upper Eocene fauna is followed by the very reduced fauna of the Lower Oligocene; then the oligocene «Grande Coupure» corresponds to a very important faunistic renewal. The fauna remains poor and little diversified during the beginning of the Middle Oligocene after which there is a new faunistic explosion. 

Is hereby described an impressive lchnoiauna belonging to the Lower to Middle Ludian of the Gard (S. France). The slab, already cleaned over a length of 18 m, is located near the top of the Potamides aporoschema lacustrine limestone (Lower Ludian, Euzet zone). It is therefore older than the Célas sandstone deposit, and still more than the Melanoides albigensis and M. acutus marly limestone corresponding to the Upper Levels of the Ludian stage. Although biostratigraphically older than the La Débruge and Montmartre zone, the biotope shows already a sampling of very tall Artiodactyles, Perissodactyles and Carnivorous. One of the most « majestic ›› Artiodactyles, Anopolotheriipus lavocati, nov., points out a huge size type. To mention also among the Ichnotypes described, 10, the big Perissodactyle Palaeotheriipus similimedius, nov., and the big Carnivorous Hyaenodontipus praedator, nov. 

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. 

A new Devonian vertebrste locality has been discovered in 1976 in the basal part of the Khush-Yeilagh Formation in the eastern Alborz Mountains of Iran. The fossils occur in a band one centimeter thick which is identifiable at other outcrops in the area. A preliminary study of the remains has yielded the following faunal list : Placodermata (Phlyctaeniida indet.. Groenlandaspididae indet.. Coccosteidae indet., Holonema sp., Ptyctodontida indet., Antiarcha indet., Bothriolepis cf. kwangtungensis), Elasmobranchii (Ctenacanthidae indet.), Acanthodii (Gyracanthus sp., « Onchus » overathensis, Ischnacanthiforme indet.), Dipnoi (? Dipteridae indet.), « Crossopterygii ›› (Onychodus cf. sigmoides, Holoptychiidae indet., Osteolepididae indet.). This fauna is older than the Middle Givetian and probably of Middle or Lower Eifelian age. Owing to its diversity, it may prove possible to use it in the future as a reference fauna for the study of the Devonian vertebrates in Central Asia and the Middle East. 

Résumé :
L’étude des rongeurs Theridomorpha permet de suivre le déroulement d’une radiation adaptative pendant toute sa durée (Eocène moyen-Oligocène terminal), sur un territoire restreint à l’extrémité ouest de l’Europe Occidentale. Dans ce papier, la phylogénie de ce groupe est établie à partir d’une analyse cladistique reposant sur l’examen de 315 caractères (310 dentaires). Le groupe d’intérêt comprend 110 des 132 espèces (24 genres) de Theridomyoidea et deux genres encore inclus jusqu’ici dans les Reithroparamyinae qui rejoignent les Theridomorpha. Les groupes externes comprennent des Glires basaux, Cocomys, Tanquammys et 16 Ischyromyiformes. Un cadre phylogénétique robuste est produit, qui permet de clarifier la systématique des Theridomorpha. La position des Remyoidea (nov. sup.fam.) au sein des Ischyromyiformes, extérieure aux Theridomorpha, est confortée. Les Protadelomys et Tardenomys sont à la base des Theridomyoidea, avant la séparation en deux clades correspondant aux familles Pseudosciuridae et Theridomyidae. Les sous-familles sont consolidées : Pseudosciurinae et Sciuroidinae pour les Pseudosciuridae ; Issiodoromyinae, Oltinomyinae, Columbomyinae, Theridomyinae, auxquelles s’ajoute au moins une nouvelle sous-famille (Patriotheridomyinae), pour les Theridomyidae. La topologie des chrono-espèces (sensu Simpson), traitées antérieurement comme lignées évolutives, apparaît dans la plupart des cas sous forme de clades successifs dans lesquels les espèces sont le plus souvent arrangées de manière pectinée, émergeant dans l’ordre stratigraphique. L’analyse des caractères aux principaux nœuds permet de consolider les caractères diagnostiques des taxons et les tendances évolutives, ainsi que de discuter des divers parallélismes et convergences dans l’évolution des structures et patrons dentaires (e.g., émail des incisives unisérié chez les Issiodoromyinae et les Patriotheridomyinae, ou pseudo-multisérié chez les Blainvillimys les plus hypsodontes, les Protechimys et Archaeomys ; patrons dentaires téniodontes ; allongement des dents déciduales chez les Patriotheridomyinae, Issiodoromyinae et Theridomyidae ; sélénodontie ou lophodontie). Les dynamiques évolutives traduites par les changements morphologiques sont mises en relation avec les variations environnementales. Enfin, les implications biochronologiques de l’évolution des Theridomyoidea sont discutées.
Abstract:
The adaptive radiation of the rodents Theridomorpha occurred during a limited time window (middle Eocene to late Oligocene), on an area restricted to Western Europe. In this paper, the phylogeny of this group is established via a cladistic assessment of 315 morphological characters (310 dental). The group of interest encompasses 110 upon 132 species (24 genera) of Theridomyoidea, and two genera formerly included within the Reithroparamyinae, and which are included here within the Theridomorpha. The outgroups include basal Glires, Cocomys, Tanquammys and 16 Ischyromyiformes. A robust phylogenetic frame is produced, which allows clarifying the systematics of the Theridomorpha. Within the Ischyromyiformes, the Remyoidea (nov. supfam.) are set apart from the Theridomorpha. Protadelomys and Tardenomys represent the earliest offshoots of the Theridomyoidea, before the dichotomy between Pseudosciuridae and Theridomyidae. It supports the former subfamilies Pseudosciurinae and Sciuroidinae within the Pseudosciuridae; and for the Theridomyidae: the Issiodoromyinae, Oltinomyinae, Columbomyinae, Theridomyinae, with at least one new subfamily (Patriotheridomyinae). The topologies of the chronospecies (sensu Simpson), formerly considered as evolutionary lineages, appear in most cases as successive clades, in which the species are generally pectinately arranged and emerging in the stratigraphic order. The analysis of characters supporting the main nodes allow consolidating the diagnosic characters of the taxa and their evolutionary trends, as well as discussing the various cases of parallelism and convergence in the evolution of structures and dental patterns (e.g., uniserial incisor enamel for Issiodoromyinae and Patriotheridomyinae, or pseudo-multiserial for the most hypsodont Blainvillimys, Protechimys and Archaeomys; taeniodont dental patterns; lengthening of deciduous premolars for Patriotheridomyinae, Issiodoromyinae and Theridomyidae; selenodonty or lophodonty).
Evolutionary dynamics are analysed with respect to environmental changes. Finally, biochronological implications of the evolution of Theridomyoidea are discussed.
  

The rodent fauna of Beni-Mellal is characterized by the abundance of ctenodactylids and cricetids. The latter are represented by four distinct species, among which a new form. Dakkamys zaiani nov. gen., nov. sp. is described. A detailed morphological analysis shows that, contrary to that which had been established before, « Cricetodon ›› atlasi Lavocat, 1961, is not closely related to any European form known; this species is attributed, in consequence, to the new genus Mellalomys. A simple biometric analysis has shown that the genus Myocricetodon Lavocat, 1952, is represented in this locality by two distinct species. The systematic homogeneity of the Beni-Mellal cricetids is also demonstrated: they can, as a matter of fact, all be referred to the subfamily Myocricetodontinae. The definition of this subfamily is completed. The sciurids and glirids are also reviewed in the light of new systematic and biogeographic information established ln Europe. A new species of Atlantoxevus from the early Pleistocene of Morocco, A. huvelini nov. sp., is described. It is probably the descendant of A. tadlae from Beni-Mellal. Biogeographic analysis leads one to consider this fauna as the result of geographic isolation in the Maghreb since the late Oligocene or the early Miocene. In particular no direct European influence can be discerned. Stratigraphic considerations resulting from the discovery of new localities in North Africa lead to the confirmation of the ante-Vallesian age of this fauna and to its parallelism with the faunas of La Grive in Western Europe and Fort Ternan in East Africa. The peculiar geologic nature of this locality is discussed.
  

The discovery of new hippopotamid material from the late Miocene Baynunah Formation (Abu Dhabi, United Arab Emirates) has prompted the revision of the existing material of this as yet unnamed fossil taxon. The Baynunah hippopotamid appears to be distinct from all other contemporary and later species in having a relatively more elongate symphysis, a feature similar to the earlier (and more primitive) Kenyapotamus. Yet, the Baynunah hippopotamid presents a dentition typical of the Hippopotaminae. It is therefore a distinct species attributed to the later subfamily, described and named in this contribution. This species provides further evidence for a ca. 8 Ma evolutionary event (termed “Hippopotamine Event”) that initiated the spread and ecological significance of the Hippopotaminae into wet habitats across Africa and Eurasia. The morphological affinities of the new species from Abu Dhabi suggest that the Arabian Peninsula was not a dispersal route from Africa toward southern Asia for the Hippopotamidae at ca. 7.5 Ma to 6.5 Ma. 

Morphological descriptions are given of Eocene mammals from the locality Toru Ajgyr (NEKyrgyzstan) that were excavated in 1997 and 1998 in a cooperation between the Martin-Luther-University Halle (Germany), the Zoological Institute in St. Petersburg (Russia) and the Seismological Institute in Bishkek (Kyrgyzstan). The species found belong mostly to perissodactyls, as Lophialetes sp., Teleolophus sp. and brontotheres. The primitive ungulate family Olseniidae is represented by a complete foot skeleton of cf. Olsenia sp. In addition, postcranial materials of Gobiatherium mirificum (Dinocerata) and of artiodactyls have been collected and are described herein. Based on mammals, the locality is part of the Asian Land Mammal Age Arshantan and is stratigraphically equivalent with the Bridgerian Land Mammal Age in North America and with the lower and middle Geiseltalian of the European Middle Eocene. 

The mammalian faunas of the Paleogene of Europe and their localities are reviewed with comments on problems of European stratigraphy (epoch, stage and substage limits) and on the possibilities of faunal migrations. Radiometric dating is discussed. A stratigraphic scale for the Paleogene is presented, as well as a refined system of sequential faunal levels. 

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.