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.
  

Pleistocene bird fossils have been studied from nine localities on Crete. Part of this material was described earlier by the author (Weesie, 1982) and will not be treated here in extenso, the results will be incorporated. More than one third of the over 10,000 fossil bird bones available could be identified ; they were found to represent at least 65 bird species. The following species of the Pleistocene Cretan avifauna are new to the fauna of Crete : Branta ruficollis, Haliaeetus albicilla, Gyps melitensis, Aquila chrysaetos simurgh n. ssp., Ketupa zeylomensis, Aegolius funereus, Dendrocopos leucotos, Zoothera dauma, Turdus iliacus and Pyrrhula pyrrhula. The Pleistocene Cretan avifauna differs less from comparable mainland avifaunas than (fossil) avifaunas from oceanic islands do. Still, the Pleistocene Cretan avifauna has two qualities that are characteristic of island avifaunas : the almost complete absence of a group of birds (the Galliformes) and the presence of two endemic (sub)species : the giant eagle Aquila chrysaetos simurgh n. ssp. and the long-legged owl Athene cretensis (Weesie, 1982). The new subspecies is described in the present study.
These endemic birds of prey were found in association with their supposedly principal prey species (now extinct as well) : endemic mice for the owl and endemic deer for the eagle. Endemic mammals have been found in association with endemic birds of prey on many islands, not only in the Mediterranean. There is evidence that the size of endemic birds of prey becomes optimally adapted to their feeding on certain endemic mammals, especially rodents. Another characteristic of the Pleistocene Cretan avifauna is the great number of species of birds of prey. This appears to be a common characteristic of fossil avifaunas from caves on Mediterranean islands as well as from caves on the European mainland. However, we think that ecological conditions on Pleistocene Crete (especially the abundant presence of mice) helped to account for the high representation of birds of prey. Furthemore, the fossil avifauna enables us to draw some conclusions about the climate and vegetation on Pleistocene Crete : it is concluded that the climate was cooler than today and that Crete was largely covered with forests. Finally, the reasons for the extinction or disappearance from Crete of some bird species of the Pleistocene Cretan avifauna are discussed. 

The present study of Artiodactyla from the Middle Eocene of the Geiseltal lignite beds concems systematics, biostratigraphy, and palaeoecology on the basis of 174 specimens: isolated remains to more complete skeletons. Instead of the formerly known five species of two families are now recognized 14 species of the Diacodexeidae, Dichobunidae, Cebochoeridae, and Haplobunodontidae. New species are Aumelasia maniai, Anthracobunodon neumarkensis, Masillabune franzeni. Four species of the Geiseltalfauna are definitely known from elswere, and five species are closely related to those from other European localities. Evidently the faunal situation of artiodactyls during the Middle Eocene of Europe was largely uniform. The distribution of artiodactyls within the sequence of the Geiseltal strata corroborates the biostratigraphical concept of the land mammal age Geiseltalian (Franzen & Haubold l986b) as well as the mammalian reference levels MP 11-13 (Franzen 1987). Reconstructions of the skulls and skeletons allow conclusions on the functional morphology and palaeoecology of the artiodactyls of the European Middle Eocene 

The study of all the available skulls allows us to review the systematic relationships of the longirostrine Steneosaurus from the Middle Jurassic of western Europe. Up to now, Aalenian and Bajocian deposits have not yielded any significant Steneosaurus remain. In the Bathonian, the only valid longirostrine species, S. megistorhynchus, is known in the Britain-Normandy Basin, the Poitou and the Lorraine. In the Callovian, most of the longirostrine Steneosaurus remains can be attributed to the species S. leedsi. Nevertheless, some remains from the Middle Callovian of Poitou (France) show important differences with S. leedsi. A new Steneosaurus species, only known in Poitou, is created and named S. pictaviensis. The specific characters are carried by the skull (preorbital pit well marked, orbit and ptetygoid fossae shapes), by the mandible (symphysis shape) and by the teeth (ornamentation). S. megistorhynchus is probably situated near the stem of the Callovian species but remains from the Bathonian and Lower Callovian are very scarce and it is very difficult to precise the phylogenetic relationships between the longirostrine species of the Middle Jurassic.
  

The object of this work is the study of the artiodactyls of the karstic locality of Lissieu near Lyon. Among the sixteen species counted, five (Hyperdichobune nobilis, Hyperdichobune sp., Haplabunodon mulleri, Tapirulus depereti and Pseudamphimeryx schlosseri) are cited for the first time in this fauna. The description of part of the anterior dentition of «Dichobune» langi permits the referal of this species to the genus Hyperdichobune. The new selenodont species Dichodon lugdunensis  described in this work belongs, with its ancestor Dichodon simplex, to a lineage distinct from that of Dichodan cartieri and Dichodon ruetimeyeri. Finally, the taxonomic reality of the Lissieu species, Lophiobunodon rhodanicum Deperet, is justified. All the other species have been compared with those of Egerkingen. Even though with most of them no difference in age can be shown between the two deposits, some however indicate clearly by their degree of evolution that Lissieu is slightly more recent than Egerkingen. ln the history of Eocene mammals, the Lissieu fauna, because of its homogeneity, can be considered as a sure reference fauna of the Auversian period. 

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 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. 

The intensive exploration of the Pliocene Hadar Formation, rich in hominid remains, led us to the discovery of several micromammals levels. ln some of them, rodents are very abundant. The stratigraphic repartition of these levels do not cover the whole fossiliferous series of the formation but takes place only in the sedimentary members from Sidi Hakoma and Denen-Dora (rancing from 3.1 - 3.2 MY to 2.8 - 2.9 MY, according to the recent geochronological data). During this gap of time, the species do not show morphological changes, what allowed us to gather, in the same taxa, forms of slighty different ages.
Two striking facts, giving a lot of indications, characterize these small rodents'faunas. First, we notice the domination of the Muridae, as well on a qualitative way (number of species) as on a quantitative one (number of individuals). Then, it appears that, until now, two genera of these murids were known only in the south-western asiatic regions. So, we can suppose continuous biotops between Africa and Indian Subcontinent before 3 MY. In this hypothesis, the hominids had already the possibility to leave their african « cradle ››. Finally, almost all studied genera are still represented at the present time. This fact, previously observed in Laetolil, Omo, Olduvai contributes to remove hope of establishing a biochronological scale based on rodents, in tropical zone. Nethertheless, that allows to try a reconstruction of the palaeoenvironnement, by using the principle of actualism.
  

The study of that locality allowed the description of a new Muridae : Paraethomys athmeniae n. sp. It reveals the existence of new rodent for Algeria : first, a Sciuridae, Atlantoxerus cf. rhodius, and second, a Gliridae, Eliomys truci. So, that work shows the presence of the genus Eliomys in North Africa before the middle of Pleistocene. Lastly, Paraethomys cf. anomalus gives an exact datation of that bed. 

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 Pantolestidae from the middle eocene of Bouxwiller are the subject of a detailed study. Buxolestes hammeli (n. g., n. sp.) is not closely related to any other European or North American form described until now; it presents, however, some characters in common with Pantolestes, a form of the same age from North America. A parallel evolution from a common ancestral form could explain this ressemblance.
Another form (gen. and sp. indet.) accompanies Buxolertes hammeli in the Bouxwiller fauna.
  

The fauna studied in the following work involves the dentitions and skulls more or less complete of 5 genera, among which only Cephalomys was previously known by its skull. One must notice that the Salla's species of this genus is a new one. Sallamys, rather small, shows a dentition rather similar to that of Platypittamys Wood from Patagonia. The upper molars, more primitive than those of this last genus, according to the smaller dimensions of the hypocone, retain a distinct metaloph. This metaloph tends to be reduced in a way which may give us a possibility to understand how it disappeared in Platypittamys. The upper P4 can be compared as well to that of Platypittamys as to that of Gaudeamus from the African Oligocene. The lower P4, more molarized than that of Platypittamys, is already moving towards the miocene type of structure. The infraorbital foramen is wide and the insertion of the masseter on the muzzle is spacious. Branisamys, genus of a great size, shows an auditory region partly preserved, peculiarly the promontorium with the fenestra rotunda, entirely of the Hystricognathi type. Upper molars are very clearly pentalophodont. A new reconstruction is proposed for the tooth called Villarroelomys by Hartenberger. This tooth is shown to be a lower D4, perhaps of Branisamys , certainly of a rather nearly allied form, and Hartenberger does agree with the essential part of this new conclusion. Of Incamys, two incomplete skulls are known, each one being admitted to be the type of a distinct species, the first one being I. bolivianus, I. pretiosus the second. The infraorbital foramen is of a great size and the impression of the masseter on the muzzle is spacious. The sphenopalatine foramen is widely developed and of a really very uncommon great size. Only Thryonomys from Africa shows a similar tendency to the enlargement of this foramen, but not so extreme. The main basicranial foramina can be observed. The upper teeth, hemi-hypsodont, show, either a vestigial metaloph, similar to that of recent Thryonomys from Africa, associated with a well developed mesoloph, either a well developed metaloph, while the mesoloph is reduced or absent. Cephalomys was previously known by anterior parts of the skull showing a wide infraorbital foramen and a spacious facial insertion of the masseter. Its lacrymal is of the phiomorph type and the spheno-palatine foramen is seemingly of great size, like in Incamys. The species is new. The varied peculiarities of the upper teeth of these genera can be easily understood if we refer to the plan of the teeth of Phiomys andrewsi from the Oligocene and Miocene of Africa. The structure of this genus, clearly more primitive, still typically brachyodont, shows and clearly explains the fundamental coherence of the varied realisations arised from such a structure. Luribayomys n.g. is known only by an anterior half of a skull without teeth. It is remarquable by the great development of the masseter's insertions on the muzzle and by the lacrymal region, well preserved, typically phiomorphid. The classification previously published by A.E. Wood and B. Patterson is granted in its essential parts, provisionally, but not as a definitive solution. Nevertheless the Dasyproctidae are integrated within the Cavioidea, following the conclusions of Bugge and of Vucetich, reached independently. The conclusion emphasizes the exceptional meaning of the fauna of Salla-Luribay. This shows that Platypittamys, while interesting, can no more be supposed certainly representative of the normal structure of the Oligocene Caviomorph, and not even of their ancestors. The anatomical peculiarities exhibited in these new samples, auditory region, lacrymal, spheno-palatine foramen, reinforce the primitive structural identity with the Phiomorpha. Similarly, the new lower D4 favour very close relationships, ever if the affinities of the D4 has been questioned or minimized by Wood and Patterson. It is certainly possible to admit that parallelism could explain limited similarities, like the presence in North America of Rodents with an hystricomorph type of infraorbital foramen and an hystricognath mandible. But if the parallelism could be a sufficient explanation of the identical association of multiple and complete structures observed in the Caviomorpha and Phiomorpha, all the Zoological systematic would have to be questioned. The last positions of A.E. Wood on the subject (1975) are revised and criticised, and the recent publications studying the problems of distance between Africa and South America in Eocene time, as a consequence of the drift, are quoted; the possibility of transportation by rafts is shown. A new hypothesis is proposed about the interrelationships of Pentalophodont Rodents, with interesting paleobiogeographic implications. 

The numerical importance of the Condylarths in the Cernaysian fauna is discussed. The Condylarth family, Tricuspiodontidae, is reviewed in the light of new material and its close relationships to the Phenacodontidae is suggested ; one new species is recognized : Tricuspiodon sobrinus. European Arctocyonidae are reviewed and the recentclassification of Van Valen is briefly commented on. Also,  the arctocyonine Landenodon is described for the first time in Thanetian (Late Paleocene) sediments ; two new species are proposed : T. lavocati and T. phelizoni. 

New and hitherto unpublished mammals from the stratigraphical levels Unterkohle, Untere Mittelkohle and Obere Mittelkohle of the Geiseltal near Halle, GDR, are described (= biochronological levels MP 11-13, Geiseltalian sensu Franzen & Haubold 1986a, b). The marsupial taxa Amphiperatherium aff. maximum (MP 12), A. goethei (MP 12), and Peratherium aff. monspeliense (MP 12 and 13) are recorded for the first time. A lectotype for Amphiperatherium giselense is designated, and the alleged primate Microtarsioides voigzi is assigned to Marsupialia, incertae sedis. A new insectivore species, Saturninia ceciliensis n. sp., is described (MP 13). The anteater Eurotamandua joresi is recorded for the first time outside its type locality, Grube Messel, FRG (MP 11). The present humerus and ulna display the autapomorphic features of the myrmecophagids. 

Reigechimys octodontiformis gen. et sp. novo and R. plesiodon sp. novo are described. They represent the frrst record of the family Echimyidae for the Cerro Azul Formation (Huayquerian Age, Late Upper Miocene) at La Pampa Province, central Argentina. Both species have hypsodont cheek teeth with an eight-shaped occlusal design. This dental morphology represents a noticeable case of convergence to octodontids and indicates that these echimyids inhabited open environments. 

Isolated upper cheek teeth of the primitive artiodactyl Diacodexis sp., upper molars of Eolantianius russelli gen. et sp. nov. (Diacodexeidae), two lower molars tentatively referred to Eolantianius russelli gen. et sp. nov., and astragali of Diacodexeidae indet. are described from the early Eocene (late Ypresian) of locality Andarak 2 in Kyrgyzstan. 

Tarsals that can be confidently attributed to Paschatheríum dolloi from Dormaal (Belgium) are described. The astragalus is short; its broad neck is set at an angle of 30 degrees to the trochlea. The trochlea is pulley-shaped and proximally extended. There is no astragalar foramen. The medial tibial facet extends distally in a cup deeply excavated in the neck and buttressed. The sustentacular facet extends toward the navicular facet but is not fully confluent with it. The calcaneum bears a proximo-distally extended proximal facet for the astragalus. A relatively large peroneal tubercle projects from the body, and is situated distally. Functionally, the trochlea indicates extensive flexion-extension movements of the foot. Calcaneo-astragalar facets indicate sliding and rotation between the two tarsals. The inclination of the navicular facet suggests frequent foot inversion. The peroneal tubercle reflects good muscular capacities for foot rotation. Overall morphology is interpreted as a scansorial adaptation similar to that of sciurids.Comparisons are made with the tarsals of Macrocranion vandebroeki from Dormaal and Hyopsodus paulus from the Bridgerian of Wyoming. Some similarities between the astragali of Paschatherium and Macrocraníon (trochlea) are interpreted as convergences for rapid locomotion. However absence of mobility at the lower ankle and midtarsal joints in M. vandebroekzi suggests that this species was cursorial, as is known for M. tenerum from Messel. Similarities in the calcanea of Paschatherium and Hyopsodus are probably the result of close phylogenetic relations, and confirm the placement of Paschatherium in the hyopsodontids. The differences in the calcanea of Paschatherium and Macrocranion underline that Paschatherium is distinct from erinaceomorph insectivores. The differences in astragalar morphology between Paschatherium and Hyopsodus show that a marked adaptive divergence separates the two genera. We speculate about the common occurrence of a deep tibial cup (“cotylar fossa”) and a pulley-shaped trochlea in Paschatherium and hyracoids, suggesting that an adaptive scenario similar to that having led to Paschatherium (scansoriality) might explain the acquisition of the peculiar hyracoid tarsal characters; such a scenario contradicts the concept of Pantomesaxonia. Other peculiar characters of Hyopsodus suggest that hyopsodontids might be given more consideration in the search for hyracoid (and tethythere) origins. 

The present work is devoted to the study of the Cretaceous and Tertiary fishes (teeth of Selachians, Actinopterygians and Dipnoans) collected during a recent expedition in Niger. The Maestrichtian localities have yielded a new genus and a new subspecies of Selachian: Igdabatis sigmodon nov. gen., nov. sp. and Lamna biauriculata nigeriana nov. subsp. The locality of Sessao, which has been attributed to the Thanetian by means of the study of the fish, has furnished by screen-washing an interesting fauna wherein six new species are described: Raja Iouisi, Dasyatis sessaoensis, D. sudrei, D. russelli, Hypolophites thaleri and Ceratodus casieri. Comparison of these faunas with contemporary faunas of Africa has brought out a certain endemism in the Iullemmeden Basin during the late Cretaceous and the early Tertiary. 

Cet article présente une étude détaillée du genre Stehlinia, un chiroptère du Paléogène d'Europe, basé sur un matériel abondant issu notamment du gisement d'Escamps (Quercy). L'analyse révèle que Stehlinia possède un mélange de caractères primitifs (comme une denture tribosphénique complète et des prémaxillaires soudés) et évolués (notamment dans le squelette post-crânien), le rapprochant des vespertilionoïdes actuels, en particulier des Kerivoula. 

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.