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. 

The fossil mammals collected from the Eocene of Hammada du Dra (northwest Sahara. Algeria) and two fragmentary teeth from the Lutetian of M'Bodione Dadere (Senegal) are described.
The fossils from the northwest Sahara come from a lacustrian deposit dated by charophytes (Raskyella aff. pecki, Raskyella n. sp.. Maedleriella lavocati, Maedleriella sp. et ? Peckichara sp.) as Middle Eocene or perhaps Lower Eocene (Gevin, Feist and Mongereau, 1974). Several hyracoids (3 or 4) identified from this formation extends the age of the family Pliohyracidae Osborn in Africa. Three forms appear to belong in the genera Megalohyrax, Titanohyrax and perhaps Bunohyrax which have been know until now only from the lower Oligocene of the Fayum (M. gevini n. sp. ; T. mongereaui n. sp.. ? Bunohyrax or Megalohyrax indet.). Another hyracoidof small size is referred to a new genus, Microhyrax (M. lavocati n. sp.).
Helioseus insolitus n. g. n. sp. is described without ordinal assignment. Azibius (Sudre, 1975) which has been the subject of questions and interpretations is reviewed.
Only one tooth from the Lutetian of M'Bodione Dadere is complete enough to interpret. lt probably belongs to a condylarth and demonstrates for the first time, the presence of the order in Africa. The second tooth is too fragmentary for comment.
In conclusion., the paleobiogeographic role of Africa at the end of the cretaceous and the beginning of the Cenozoic is discussed. 

The comparative morphology and biometry of the lower cheek teeth of modern Equus are studied on approximately 300 mandibles belonging to the 10 usually recognised species : Equus grevyi, E. burchelli, E. quagga, E. zebra, E. africanus, E. asinus, E. hemionus, E. klang, E. przewalskii, E. caballus. The studied parameters comprise : occlusal length and width, postflexid length and index ; shape of the double knot (metaconid + metastylid + lingual groove) ; depth of the vestibular groove on the molars ; frequency of the pli caballinid, protostylid and other enamel plications or islets ; frequency of the dP/l.
The same methods of study are applied to a number of North American, Eurasian and African species. For the sake of comparison, some Hemphillian equids were observed (Dinohippus interpolatus, Dinohippus leidyanus, Astrohippus ansae, Phiohippus mexicanus) but most of the discussed material belongs to Pliocene or Pleistocene species of Equus : the « stenonine ›› E. stenonis, E. simplicidens, E. sanmeniensis and E. teilhardi; the « caballine ›› E. scotti, E. lambei, E. Iaurentius, E. mosbachensis, E. germanicus, E. gallicus, E. taubachensis and the Liakhov horse. The relationships of other species, in particular the North American E. calobatus, E. occidentalis, E. cf mexicanus are not clear for the moment. ln Africa, the Plio-Pleistocene species from Koobi Fora (Kenya) show some stenonine and perhaps asinine affinities. The relationships of E. numidicus and E. tabeti are uncertain but these species are probably related to the East African ones. E. mauritanicus is most certainly related to the Quagga group.
The biometrical data are gathered in 32 tables ; 4 photographie plates and 19 figures illustrate the next. The whole is a complement of the previously published studies of the skulls, upper cheek teeth, incisors and metapodials of modern and fossil Equus.

  

Etude sur les vertébrés inférieurs (VIIe Symposium International, Parc de Miguasha, Québec, 9-22 Juin 1991), édité par Marius ARSENAULT, Hervé LELlÈVRE & Philippe JANVIER, 1994. Bulletin du Muséum National d'Histoire Naturelle, Paris, 4e Série, T. 17, Section C, n° 1-4, 529 p.

Ce volume spécial du Bulletin du Muséum réunit les actes du congrès international sur les Vertébrés inférieurs qui s'est tenu au Québec en 1991. 

La faune de Rongeurs d'Escamps (Lot) bien que relativement pauvre en espèces (dix) s'avère riche d'enseignement pour les Rongeurs de l'Oligocène inférieur d'Europe Occidentale. Cette periode semble caracterisée par une cladogenèse des Théridomyines. A Escamps, un nouveau genre (Patriotheridomys) est décrit ainsi qu'une nouvelle espèce de Theridomys. Avec Oltmamys platyceps, décrit ici plus complètement et désormais bien situé stratigraphiquement, les deux espèces précédentes constituent un ensemble original du Sud de la France. A la même époque, en Angleterre, Allemagne et Espagne, des espèces «régionales» de Théridomyinés se dersifient.  A côté de ces formes qui ne semblent pas franchir la «Grande Coupure» sont représentées deux lignées d'Issiodoromyinés (Elfomys sp et Pseudoltmomys cuvieri), une de Théridomyiné (T. (Blainvillimys) rotundidens) ainsi qu'un Gliridé, Gliravus priscus (que l'on différencie nettement de la deuxième lignée des Gliravus oligocènes : G.  meridionalis -> G. majori). On retrouve ces formes dans les gisements plus récents du niveau de Hoogbutsel où elles sont à peine plus évoluées. Le fait que les degrés évolutifs de ces lignées soient très proches laisse supposer que le laps de temps séparant les niveaux d'Ecamps et Hoogbutsel fut relativement court. 

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 classification should be both usable and useful,not too complex either in the amount of splitting or in the number of hierarchies involved, and not so simple as to give a false assurance of knowledge of relationships. Classifications are only possible because we do not have complete knowledge of the evolution of the organisms concerned because gaps in the record are necessary to allow the separation of the various taxa. Rodent classification is complicated by the large number of organisms involved and by the geat amount of parallelism that has taken place in the evolution of any and all features. If several independent features are characteristic of a certain taxon, should an effort be made to define the group on the basis of all the features, or should only one be selected as the determinant ? Unless the evolution of the several features was closely linked, the former solution will sooner or later lead to insurmountable problems. 

Description, for the first time, of the skull of Ruscinomys Depéret on the basis of a nearly complete specimen, and description of a new facial part of a Megacricetodon Fahlbusch skull (material from upper Miocene, Spain). New description of the skull (facial part) of " Cricetodon" incertum Schlosser on the basis of the specimen from the Oligocene of Quercy phosphorites already published by S. Schaub.
Comparison of the skull of “ C. ” incertum with that of the asiatic genus Cricetops Matthew and Granger and that of the North-American Eumys Leidy. These three genera of similar age display very distinct characteristics; their common origin must go back to the Eocene, as Wood believed.
Comparisons of the auditory regions of Ruscínomys and of Megacricetodon where important differences are noted. Comparison of the Cricetodontines from European Miocene with contemporary Cricetines. Contrary of the opinion held by Schaub, their anatomical differences do not seem suflicient to warrant the contention that none of the Cricetines derive from a form close to one of the known Cricetodontines. 

This paper is about the oldest African rodents faunas, from the late Early Eocene, or early Middle Eocene, Glib Zegdou (Algeria) and Chambi (Tunisia) localities. Five species are described and figured, belonging to a new family here created, the Zegdoumyidae.

This family is compared to the Early and Middle Eocene rodents families from Asia, Europe and North America (Chapattimyidae, Yuomyidae, Gliridae, Theridomyidae, lschyromyidae and Sciuravidae), as well as to those known from the Late Eocene African locality Bir El Ater (Anomaluridae and Phiomyidae).

On the one hand, it seems clear that the African endemic Anomaluridae arise from the Zegdoumyidae. On the other hand, the lschyromyidae, or primitive Sciuravidae, may be the most reliable ancestral groups for the Zegdoumyidae. Thus, this new family can be considered as the sister group for the American Sciuravidae on the one hand, and for the European Gliridae on the other hand.

The biogeographical consequences of these phylogenetic hypotheses are discussed. A new phase of communication between Europe and North Africa is inferred, during the Early Eocene. It has been followed by a short period of endemism, allowing the adaptive radiation for the Zegdoumyidae, preceding the immigration of the Phiomyidae, during the Late Eocene, probably from Asian relatives.