The recent discovery of several mandibular toothplates of a chimaeroid fish at a dig in the area of the Landover Mall, near Landover, Prince Georges County, Maryland, brings to our attention a new species of the chimaeroid, Ischyodus.
 Although superficially reminiscent of the European chimaeroid toothplates of Ischyodus thurmanni (cf. text-fig. 2), I. williamsae nov. sp. probably has a more closer relationship to I. bifurcatus CASE, 1978, of the Upper Cretaceous of New Jersey and Delaware. 

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.

  

The utilization of screen-washing and attack by dilute acetic acid has permitted the collecting, in the Miocene of the department of Hérault (France), of a very rich ichthyofauna. This fauna is presently comprised of about 60 studied species, of which 11 are new, and represents, in the present state of knowledge, the most varied Miocene selachian fauna described in the world.
The abondance of material has allowed an overall revision to be made; it has thus been possible to complete the description and the figuration of species that were poorly known until now, and to synonymize species that were established on simple morphotypes. Paleo-ecologic study of the ichthyofauna has permitted conclusions to be drawn relative to climate and bathymetry; it was thus possible to show that the Miocene fauna of Hérault was a fauna of a subtropical sea, essentially neritic with rare pelagic contributions.
Knowing the stratigraphic position of the localities, it has been possible to distinguish three faunal assemblages based on associations of species. Some hypotheses on the evolution of certain lineages have been expressed.
The comparison of this fauna with that of other regions permitted the relationships of two diflerent faunal provinces to be specified: the first belongs to the northern domain, characterized by a fauna still subtropical but with numerous temperate water elements; the leoond belongs to the Mesogean domain characterized by warm water forms. It has also lhovm that contemporary faunas could be very different according to the bathymetric zone in which they lived, which furnishes valuable information for the paleogeographic reconstruction of sedimentary basins.
  

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. 

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. 

A new hypothesis for the phylogenetic relationships of recent anomalurids and graphiurids is proposed, based on information from evolutionary lineages of Paleogene European rodents, particularly Gliridae, and Eocene Algerian Zegdoumyidae. Differences in first occurrences, in paleogeography, and in infraorbital structure in glirids (protrogomorphy and pseudomyomorphy) and graphiurids (hystricomorphy) separate Graphiuridae from Gliridae (Graphiurinae is here raised to family rank). Similar considerations, and dental morphology, suggest that Anomaluridae (appearing in the late Eocene) and Graphiuridae (appearing in the Pliocene) are related to early Eocene Zegdoumyidae. 

Extensive collecting in previously known and new Middle Eocene rodent localities in the Subathu Group of the Rajauri and Reasi districts, Jammu and Kashmir (northwest Himalaya, India) has yielded over 500 isolated cheek teeth, numerous incisors and cheek tooth fragments, and two mandibular fragments with M/1-M/3. An analysis of this additional material and a restudy of that reported earlier from the Metka (Rajauri) area has revealed the presence of diverse Middle Eocene ctenodactyloid rodents in India. The assemblage comprises six genera and twelve species, viz.., Bírbalomys woodi, B. ibrahimshahi, B. sondaari, Basalomys vandermeuleni, B. ijlsti, B. lavocati, Chapattimys wilsoni, C. debruijni, Gumbatomys asifi, cf. Advenimus bohlini, cf. Petrokoslovia sp. indet. 1 and cf. Petrokoslovia sp. indet. 2. Most species of this assemblage are endemic to the Indian subcontinent and are referred to the Family Chapattimyidae. However, at least three taxa, viz.., cf. Advenimus bohlini, cf. Petrokoslovia sp.indet. 1 and cf. Pezrokoslovia sp. indet. 2 show close affinities with their Central and Eastern Asiatic contemporaries and are attributed to the Family Yuomyidae. The dentitions of most of the Middle Eocene rodents from India are described here in better detail thus providing more precise characterization than was available earlier. The taxonomie status of Basalomys, formerly a subgenus of Birbalomys has been raised to that of a genus. Basalomys vandermeuleni is here designated as the type species of Basalomys in place of B. ijlsti. The rodent assemblage from the Subathu Group is specifically similar to that from the coeval Kuldana Formation of Pakistan. The absence of Birbalomys ibrahimshahi and cf. Advenimus bohlini in Pakistan is related to sampling bias. The identifications of the Early Eocene rodents from Barbara Banda, Pakistan have been reexamined and the familial assignments of some of the Early and Middle Eocene rodents from Central and Eastern Asia have been discussed and reviewed in the light of recent discovery of early rodents in Mongolia.

  

Rodents from the new localities of Châteauredon (Alpes-de-Haute-Provence) and La Denise (Bouches-du-Rhône) show more similarities with the rodents known from the Czecho-Slovak locality of Franzenbad than with the species found in contemporaneous Lower Miocene faunas located westward of the present Rhône Valley. This is another data wich support the existance of several biogeographical provinces in Southern France during Lower Miocene. The correlations which have been settled down allow new datations of several formations in Provence and give new information on the Aquitanian and Burdigalian paleogeographies of this region. More precise stratigraphical allocations are given to some other localities of Central Europe. 

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. 

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.
  

Anthracotheres from the Pondaung Formation, Myanmar, are considered as one of the most primitive artiodactyl groups and they represent the oldest known record in the world. Thus, the understanding of this group has numerous implications for evolutionary biology and biochronological correlations. However, the systematlcs of these mammals has been interpreted in different ways, and the main debate focuses on the number of taxa represented in the Pondaung Formation. The revised taxonomy proposed here is mainly based on the relative development of the upper molar W-shaped ectoloph, system of crests and stylar cusps, and on body size. On the basis of these characters, they are classified into four genera including six different species. Two well-known genera, Anthracotherium and Anthracokeryx, are validated and more precisely diagnosed. Anthracokeryx possesses a better developed W-shaped ectoloph, system of crests and stylar cusps than Anthracotherium, which displays notable differences with the more derived representatives of this genus. Both of these Pondaung genera show evidence for sexual dimorphism. However, the incompleteness of fossil material fueled a debate concerning the status of two additional Pondaung anthracotheres, Siamotherium and Anthracohyus. The latter genus is of uncertain affinities, but it has been considered as a hippopotamid ancestor. Despite new material attributed to these two forms, additional discoveries are still required to establish their taxonomic status. The hypothesis that Southeast Asia was the centre of origin of Anthracotheriidae is supported by the retention of numerous primitive dental characters in these taxa and by the antiquity of the Pondaung Formation, to which an age of 37 My is now generally accepted. 

The knowledge of the Anchilophini has been lately renewed by the discovery of a rather large amount of new material still largely unpublished. This new material offers the opportunity of a systematic revision of this tribe gathering those of European Eocene Equoidea which bear no mesostyle on upper check teeth and display a heavy trend to the molarization of premolars.

A cladistic analysis has made out two genera, Anchilophus (Paranchilophus included as a subgenus), characterized by a marked lophodonty and the transverse narrowness of the cheek teeth, a rather high hypsodonty, the frequent occurrence of "crochets" and "anticrochets" on the superior ones, and a rather weak molarization of the premolars, opposite to Metanchilophus n. gen. whose cheek teeth are more transversally elongated, less high, less lophodont, with cusps better distinct, enamel thicker and premolars more molarized on the whole.

Three species of Anchilophus are recognized, A. desmaresti, type species of the genus, A. (Paranchilophus) remyi and A. (Paranchilophus) jeanteli n. sp.

The genus Metanchilophus is more diversified with the species dumasi, radegondensis, gaudini (whose a new sub-species M. g. fontensis is defined), depereli, castrensis n. sp. and chaubeti n. sp.

The skull anatomy has been moreover described with several taxa; it brings to light (for all that one can generalize) that Anchilophini were light animals with a slender and elongated snout, a thin zygomatic arch, a rather developed encephalon with an advanced gyrencephaly.

The structure of the nasal opening together with the occurrence of epitympanic sinuses and the molarizing process of the premolars corroborate the attribution of this tribe to the family PalaeotheIiidae. 

The genus Parasteiromys AMEGHINO, 1904 is revalidated, and P. friantae sp. nov. (Hystricognathi, Erethizontidae) from Colhuehuapian (early Miocene) sediments of the southern cliff of Colhue-Huapi Lake (Province of Chubut, Argentina), is described. The molar morphology of these taxa and of living porcupines adds new elements to understand the dental evolution of the Erethizontidae, and to propose the hypothetical ancestral molar pattern for this family. This pattern does not correspond to any of the morphologies traditionally proposed as ancestral for South American hystricognathous rodents. The proposed pattern is characterized by a metaloph disconnected from the posteroloph and oriented towards the hypocone, and the third loph incompletely developed with the lingual portion homologous to the mesolophule of Baluchimyinae (Chapattimyidae) from the Miocene of Pakistan. The inferred steps of the molar evolution of erethizontids towards the pentalophodont condition, considered derived for the family, are illustrated. This study strengthens the hypothesis placing erethizontids in a basal position among rodents of the suborder Hystricognathi.

  

The Condylarths from Hainin (Hainault, Belgium) show no affinity at the generic level to those known in other Paleocene localities of Europe and North America ; they are described as new forms : Monshyus praevius n. gen., n. sp. and Prolatidens waudruae n. gen., n. sp. Monshyus praevius, discovered in only one of the levels in the excavation at Hainin, is similar to the genera Microhyus TEILHARD and Louisina RUSSELL ; with them it is included in the subfamily Louisininae (Hyopsodontidae). With respect to Microhyus and Louisina, Monshyus is distinguished by the precociously modern aspect of its upper molars, the only teeth that are referable. Prolatidens waudruae, known only by lower molars, was found in several levels in the pit at Hainin. It is an arctocyonid presenting possible relationships to the North American form Oxyprimus galadrielae ; it therefore has been provisionally attributed to the subfamily Oxyclaeninae. If this attribution is confirmed, this species will constitute the first and only representative of the group in Europe. 

The oldest european marsupials are described from some specimens (isolated upper molars) recently found from the Hainin sediment (Middle Paleocene of Belgium). These fossils document a new species of the Peradectes genus. They give evidence of a much older occurrence of the marsupials in Europe than it was assumed. They allow us to postulate a didelphid dispersal from South America towards the western-holarctic area operating in two phases : the first one of the Peradectes genus at the end of the Cretaceous; the second one of the Didelphíni tribe at the end of the Paleocene. A central american crossing is likely for the first one,  whereas a transafrican way is tentatively argued for the second one. 

A fragmentary mandible and maxilla of a small sized Agriotherium of a young individual discovered from a Pliocene fissure filling in Xiaoxian county (Anhuei Province, China) are described. Judging from the morphology of the dentition and its dimensions the new material can be identified as Agriotherium inlermedium (STACH l957). Hendey's proposition (1980) that the Agriotherium species are derived from Indarctos is reconsídered on the basis of the new documents. As a result of a more general phylogenetic discussion it can be stated, that: 1. the supposed size increase as well as other trends, leading from Indarctos to Agriotherium are untenable ; 2. there are no positive indications to assume a phylogenetic transition of these two genera. 3. there are no real arguments in favor of an adaptational reversal in the evolution of Agriotherium. Hence, many features of that genus supposed by Hendey to be derived are plesiomorphic ; 4. regardless of the previous points it is methodologícally impossible to establish direct ancestor - descendant relationships between Indarctos and Agriotherium species, as Hendey did. Based on the data available and especially on the characters of the new material from China it is more likely that Agriotherium and Indarctos are two genera which developed independently. While advanced Agriotherium species, e.g. A. africanum, resemble in some respects Indarctos by adaptational analogies, more primitive species, e.g. Agriotherium intermedium, are quite dissimilar to lndarctos. While Indarctos might be derived from an Ursavus like forerunner, Agriotherium has its roots more likely somewhere in between Ursavus and the Hemicyon-group. 

The Montian locality of Hainin (Hainaut, Belgium) yielded about twenty teeth of Multituberculates. They are very peculiar forms, showing no affinities, at the generic level, with those hitherto known from North America, Asia and Europe. They are referred to the new taxa Boffius splendidus nov. gen., nov. sp., Hainina belgica nov. gen., nov. sp., and H. godfriauxi nov. gen., nov. sp. They expose some common features, such as the advanced type of first upper molar. possessing at least three complete rows of cusps. Because of this, and also of the upper premolar reduction, Boffius splendidus appears as the most specialized form within the Ptilodontoidea suborder.
Several other characters of Hainina seem to be less advanced, such as the great number of upper premolars and the simple cusp-formula of the first lower molar.
Till now, only H. godfriauxi has been recovered within the Thanetian fauna from Cemay-les-Reims, where it is very poorly documented. 

Two steps can be distinguished in the history of the first invasion of western and south western Europe by the arvicolines. The first step corresponds to the installation of these rodents with the immigration of Promimonys inxuliferus Kowalski, then of Mimomys stehlini Kormos and of Mimomys gracilis (Kretzoi). The second is characterized by the establishment of a geographic differentiation in the arvicoline fauna between the south of France and Spain, from where are described new species of Mimomys (Mimamys cappettai, Mimomys septimanus, Mimonys medasensis), and the rest of France, where are found only elements already known from central Europe or England (Mimomys polonicus Kowalski, Mimomys pliocaenicus F. Major, Mimomys reidi Hinton, or forms very close to the latter). This geographic differentiation, which is very certainly the consequence of the division of Europe into distinct climatic provinces, one of them being the southern province comprising at least Spain and southern France, could result from a cladogenetic evolution of Mimomys stehlini and Mimomys gracilis after their immigration. The present work is also a contribution to the search for correlations between the diverse micromammal localities of the latest Pliocene (or early Villafranchian) and of the early Quaternary of Europe. 

Simpson (1937a) reconstructed the brain of the Paleocene multituberculate Ptilodus as having the olfactory bulbs widest anteriorly, an unusual condition among mammals. Slight preparation and reexamination of the endocast specimens of Ptilodus reveals that the olfactory bulbs in fact taper anteriorly, as in the recently-described endocranial casts of three multituberculate species from the Late Cretaceous of Asia, and as in those of other mammals. The brain of Ptilodus was therefore essentially of the same general pattem as in other multituberculates. Ptilodus differs, however, in having the vermis more deeply inserted between the cerebral hemispheres. Other details concerning the endocast morphology of Ptilodus are clarified.

The encephalization quotient (EQ) of Ptilodus is recalculated from revised estimates of both endocranial volume and body mass to fall somewhere within a broad range of values; from 0.41 to 0.62 if the olfactory bulbs are included and from 0.37 to 0.55 if they are not. In any case, the relative brain size of Ptilodus is roughly equivalent to that of Chulsanbaatar, the only other multituberculate for which EQ has been calculated, but considerably smaller than that of an average extant mammnal. 

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.