The study of new specimens from the Stephanian shales of Montceau-les-Mines confirms and enlarges the number of groups already known in this area. Among the Palaeonisciforms, “form A" is now known more completely, although no diagnosis or name can yet be given for it. “Form B" is redescribed and its relationships with “Elonichthys robisoni" are discussed. A palaeoniscid is recorded which resembles those from Bourbon l'Archambault. The paramblypteriforms occur rather frequently, but no genera can be determined. The aeduelliforms comprise some specimens close to Aeduella blainvíllei from Muse (Autun basin), and a new genus. Comparison of the latter with two fossils from Lally allows creation of two new species and a new family. This diversification of the aeduelliforms during this middle Stephanian leads to the hypothesis that the group originated at least as early the lower Stephanian. This material prooves again the characteristic endemism of this fauna, particularly of the aeduelliforms which are known only in the Massif Central where they diversified during the Permo-Carboniferous. Biogeographical consequences are discussed. 

New records of terrestrial mammals from the Qasr el Sagha Formation, Fayum Depression, Egypt are reported, and the stratigraphic occurrences of these fossils noted. These include additional specimens of Moeritheríum, Barytherium, and anthracotheres, as well as the oldest record of a hyracoid in the Fayum.These Eocene mammals occur almost exclusively in the alluvial deposits of the Dir Abu Lifa Member of the Qasr el Sagha Formation and show close affinities to the faunas from the lower sequence of the Jebel Qatrani Formation. There is no evidence of a more marked faunal discontinuity between the Qasr el Sagha and Jebel Qatrani Formations than there is across any of the three major breaks in sedimentation that exist within the Jebel Qatrani Formation. The faunal similarities between fossils of the lower sequence of the Jebel Qatrani Formation and of the upper part of the Qasr el Sagha Formation is consistent with recent paleomagnetic dating that suggests that these rocks differ in age by only one to two million years. 

Some new material of percrocutas from the late Miocene of Axios valley (Macedonia, Greece) is studied. They have been found in the locality of "Pentalophos 1" (PNT). The material has been described and compared with the known late Miocene percrocutas of Eurasia. This comparison indicates that it can be identified as Dinocrocuta gigantea (SCHLOSSER, 1903). A maxilla of a percrocuta, named ”Hyaena" salonicae, was found in the same area (Andrews, 1918). "Hyaena" salonicae is smaller than the PNT material. It is also compared with other material from Eurasia while its taxonomic and age problems are discussed. It belongs to Dinocrocuta and shows close relationships with D. robusta and D. senyureki; its age can be considered as late Vallesian-early Turolian. The age of the locality PNT is also discussed and a possible Vallesian age is proposed for it. 

The Mont-Hélène's fauna [Pyrénées-Orientales, France], includes 15 species of rodents with a new one, Occitanomys montheleni n. sp. among the 9 species of the Murids which are listed. The uncommon Cricetid, Blancomys neglectus, is well represented in the fauna. Peculiarities of the population referred to Slephanomys cf. donnezaniare discussed. The locality a fissure filling may be the oldest one of Tabianian age known in Southern France. The diversity of the Murids gives evidence of a subtropical climate and of a diversified environment which may be linked to the spreading of the coastal plain following the filling up of the Roussillon Neogene Basin. 

The presence of cambaytheres, the sister group of perissodactyls, in western India near or before the time of collision with Asia suggests that Perissodactyla may have originated on the Indian Plate during its final drift towards Asia. Herein we reinforce this hypothesis by reporting two teeth of the first early Eocene tapiromorph Perissodactyla from the Cambay Shale Formation of Vastan Lignite Mine (c. 54.5 Ma), Gujarat, western India, which we allocate to a new genus and species, Vastanolophus holbrooki. It presents plesiomorphic characters typical of the paraphyletic “Isectolophidae,” such as small size and weak lophodonty. However, the weaker hypoconulid and low paralophid, higher cusps, lower cristid obliqua, and the lingual opening of the talonid are found in Helaletidae, the most primitive tapiroid family. V. holbrooki, gen. et sp. nov., may be the oldest and the most primitive tapiroid, suggesting that at least tapiroid perissodactyls originated on India. 

In dilambdodont molars the primitive crest between paracone and metacone (centrocrista) is represented by a pair of crests that join the mesostyle (postparacrista, premetacrista). The cutting action of these crests against the crests of the hypoconid is described. Dilambdodonty is a derived adaptation for greater cutting efficiency. It has evolved several times and in more than one way. 

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. 

This study describes four taxa of Gliridae from the Oligocene mammal locality Gröben 3: Gliravus tenuis BAI-ILO, 1975, Bransatoglis micio (MISONNE, 1957), B. planus (BAHLO, 1975) and B. heissigi n. sp. Gliravus tenuis from Gröben 3 is somewhat more advanced than the type population found in Heimersheim. This confirms previous research suggesting that Gröben 3 should be dated earlier than Heimersheim (MP 24). The first documented occurrence of B. mício around level MP 24 was found in Gröben 3. An abundance of tooth material from B. planus in Gröben 3 makes it possible, for the first time, to observe evolutionary stages within this species from MP 21 until MP 28. B. heissigi n. sp. is restricted to level MP 24. This species is located between B. mísonnei (MP 20 - 23) and Microdyromys praemurinus (MP 25 - 28). Within the lineage Bransatoglis bahloi - B. misonnei - B. heissigi, a decrease in size is noticeable.

  

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. 

Prolagus sardus is the last representative of the diverse lineages of European endemic ochotonids. It is also the most abundant in the collections. The previous studies made of this species have established rather well its dental morphology, its phylogenetic position, its geographic and temporal distribution, and its intraspecific individual variation. On the other hand, no osteologic study has fully utilized the superb material from Corsica and Sardinia  collected by Forsyth Major.
Nearly all of the parts of the skeleton are represented in this material; they are here described and figured. Comparisons are made with Ochotona, the only surviving genus of the family, as well as with the living leporids, in particular Romerolagus, Oryctolagus and Lepus. A brief examination of the dentition reveals some particular characters of the incisors. The osteologic study allows limited interpretations to be advanced concerning the posture, mastication. locomotion and some other adaptive features of P. sardus.
P. sardus appears as an incontestable ochotonid, but it differs from Ochotona by some characters which are found in leporids. Certain of the characters are here judged primitive for lagomorphs. The genus Ochotona therefore can no longer be considered as the image of a primitive lagomorph, because in spite of the lack of cursorial adaptations which differentiate it from leporids, it presents other specializations which are common to it alone. 

The classifications of the recent vespertilionine bats were made wihtout taking in account the teeth morphology; this resulted in a reduction of the possibilities of comparison with the available fossils. The generalized use of dental formulae was abusive: this contributed to the admission of artificial genera. These conditions have long delayed the consideration of characters able to frame the phylogeny of the sub-family. In the first part of the study, the teeth morphologies are described and analysed. morphological reference types are established for each upper and lower tooth: they should make an easier elaboration of criteria for the differentiation at generic level. The position of the species in view of these criteria allows one to group them into homogeneous genera, and to appreciate the degree of relationship that the latter have between them. The second part of the study (next publicationà will develop inferences dealing with systematics and phylogeny 

The description of original material of anthracothere and proboscidean in the new locality of Bir el Ater 3 from East Algeria, and a thorough review of early Libycosaurus remains of Bir el Ater 2 allows us validating L. algeriensis as the smallest and earliest species of Libycosaurus and probably the earliest migrant of the genus from Asia. The presence of a Tetralophodon in the Neogene Nementcha formation might represent the earliest occurrence of the genus in Africa. These original fossil remains allow us to discuss the age of the Neogene part of the Nementcha formation close to the Serravalian/Tortonian boundary. 

The dentition of Welcommia bodeuri nov. gen. nov. sp. from the Valanginian of Southem France is described and reconstructed. Species and genera of Upper Jurassic and Lower Cretaceous Hexanchiformes are reviewed and discussed.
The genus Notidanoides MAISEY, 1986 must be restricted to the single Nusplingen Upper Jurassic specimen, whose attribution to the species muensteri AGASSIZ, 1843 remains doubtful.
The genus Paranotidanus WARD &THIES, 1987 that does not rest on any type-species nor on any precise dental characterization must be rejected.
The genus Eonotidanus PFEIL, 1983, based on a very poorly preserved and heterogeneous type-material must also be rejected.
Teeth from the Lower Cretaceous, with a peculiar morphology, previously assigned to Eonotidanus or to Notidanoides, are to be ranked in the new genus Pachyhexanchus. 

The artiodactyls (Mammalia) from the latest Ypresian locality of Prémontré from the Paris Basin (niveau repère MP 10 in the lower Eocene of the Paris Basin) are described in this paper. Three species have been identified: 1) Diacodexis cf. varleti SUDRE et al., 1983; 2) a new species of Eurodexis ERFURT & SUDRE (E. russelli nov. sp.) defined after the revision of the species Messelobunodon? ceciliensis from the Lutetian beds of Geiseltal (Germany); and 3) Eurodexeinae indet., a probable ancestor of another form from the Geiseltal which was previously recorded as Homacodon? sp. (Erfurt 1993) and now named Parahexacodus germanicus. The two later forms are referred to the new subfamily Eurodexeinae (Erfurt & Sudre 1996). The analysis of these forms as weIl as comparative studies have led us to reconsider our previous conclusions regarding the content of the species Protodichobune oweni LEMOINE 1878 and some aspects of Ypresian diacodexid evolution. One can postulate that the divergence of E. russelli nov. sp. occurred during the first radiation of these primitive artiodactyls. Some other stem form with bunodont teeth such as Protodichobune and Aumelasia have also differentiated from Diacodexis. Like Eurodexis, these two genera persist during the middle Eocene. The absence of Protodichobune and Aumelasia at Prémontré is probably due to particular ecological conditions. 

The status of the giant bird taxa Liornis floweri and Callornis giganteus from the Santa Cruz Formation (late Early Miocene) of Patagonia, first described by Ameghino (1895) is reassessed on the basis of a re-examination of the type material at the Natural History Museum, London. Liornis floweri, which lacks a Pons supratendineus on the tibiotarsus and has an unbifurcated Canalis interosseus distalis on the tarsometatarsus, is clearly a brontornithid and is considered as a junior synonym of Brontornis burmeisteri. Ameghino’s replacement of Callornis by Eucallornis is unjustified. Callornis giganteus is a chimera based on a phorusrhacid tarsometatarsus (probably belonging to Phorusrhacos longissimus) and a brontornithid tibiotarsus. The latter can be considered as the lectotype of Callornis giganteus, which may represent a small morph of Brontornis burmeisteri or a distinct taxon. It is referred to here as Brontornithidae indet. The tarsometatarsus described by Dolgopol de Saez (1927a,b) as Liornis minor and considered by her as a gracile brontornithid apparently has a bifurcated Canalis interosseus distalis and should therefore be placed among the Phorusrhacidae. 

Valverde's cenogram method is used to analyse mammalian communities from the late Eocene to late Oligocene of southern France, mainly from the "Phosphorites du Quercy". Cenogram analysis involves plotting the size of each component species in a fauna on a semilog diagram in rank order, permitting fossil faunas to be compared with Recent ones. The configurations of Recent communities serve as models for establishing the general environmental characteristics of fossil mammalian faunas. This method of analysis applied to faunal sequence can reveal major and sudden ecological perturbations. The paleobiogeographical event (i.e. the mammalian immigration wave) at the Eocene-Oligocene Boundary in western Europe, known as the «Grande Coupure", is here shown to represent a drastic and sudden ecological change: late Eocene tropical environments in Europe deteriorated rapidly turning to subdesert or desert environments al the beginning of the Oligoccne. 

A systematic analysis of an hipparionine horse assemblage from Maragheh, Iran is made. A brief orientation to systematic philosophy and informal superspecific characterizations of some Old World hipparionines is given as a background to this work. A character state analysis of skulls is made, and has revealed five distinct species. A character state and stratigraphic trend analysis of isolated check tooth and postcranial remains, with known provenance, is also made. These two combined analyses reveal that the most resolute discrimination of hipparionine species and their evolutionary relationships occurs when multiple character complexes of associated skulls, maxillary and mandibular dentitions are made. When this is not possible, skulls have provided the best basis for discriminating species and their evolutionary relationships. Traditional characters of isolated cheek teeth and postcranial remains are shown here to offer limited information content for hipparionine phylogenetic systematics. The systematic portion of this study includes a comprehensive description of cranial and postcranial remains, and has further corroborated the distinction of five species which belong to at least three superspecific groups including: «Hipparion» geltyi sp. nov., Group 1; Hipparion prostylum (s. l.), and Hipparion campbelli sp. nov., Group 3; «Hipparíon» aff. moldavicum and «Hipparion» ?matthewi, Group 2. These species stratigraphic ranges and evolutionary relationships are also given here and argued to be important for establishing future hipparionine geochronologic correlations between a number of Eurasian late Miocene provinces. 

A fossil fish fauna, based on 5533 otoliths, from the La Paillade locality at Montpellier is described and figured. The otolith-bearing marls correlate to mammal zone MN l (Aguilar, 1982), and thus represent the earliest Miocene. The fish fauna consists of 30 taxa belonging to 20 families. Two species are new: Dussumieria sittigi and Liza gaudanti. The predominant faunal element is the Lesueurigobius vicínalis-species complex, composing 73% of all investigated otoliths. The palaeoecological analysis reveals a marine to euryhaline fish fauna living under tropical to subtropical conditions in the transition zone littoral - sublittoral. Water depth probably was more than 10 m. The scarcity of pelagic físhes suggests that the habitat was either a sheltered bay and/or far away from the open sea. Furthermore, some genera represented in the La Paillade fish fauna presently live exclusively in the Indopacific realm. Their presence strongly supports a broad connection between the Indian Ocean, the Mediterranean, and the Paratethys Seas during the Early Miocene (Aquitanian). From a palaeobiogeographical point of view, faunal relationships were found between the La Paillade fish fauna and both the Paratethys fish fauna and the fish fauna from the deposits in the Upper Rhinegraben and the Mayence and Hanau Basins (Germany).



  

The first good skeletal remains of Homogalax protapirinus from the Wasatchian of the Bighorn Basin, Wyoming, indicate that this primitive tapiromorph was more plesiomorphic in many features than primitive equoids including Hyracotherium. Compared to Hyracotherium, Homogalax more closely resembles Phenacodonta (the closest outgroup of Perissodactyla for which postcrania are known) in various details of articular surfaces, muscle attachments, and proportions of the humerus, manus, and pes.Among known taxa, Homogalax most nearly approximates the plesiomorphic postcranial skeletal anatomy of Perissodactyla. 

The anatomy of Norselaspis glacialis n.g., n.sp., a primitive kiaeraspidian from the Lower Devonian of Spitsbergen, is described on the basis of spécimens studied by grinding sections or prepared with dilute formic acid. This study yielded some new anatomical details, including the presence of a canal prolonging posteromedially the canal alloted to the facial nerve by Stensiö. This posterior prolongation of the « facial canal ›› into the posterolateral part of the labyrinth cavity is consistent with the hypothesis put forward by Allis, Lindström, Jefferies and Whiting, that this canal housed the glossopharyngeus nerve. Furthermore, in N. glacialis, the foramen usually referred to as the foramen for the œsophagus opens posteriorly into a cavity in the postbranchial wall, referred to here as the intramural cavity, and which is interpreted as having housed the heart. Consequently, the œsophagus probably accompanied the dorsal aorta through the aortic canal. Finally, the foramen generally interpreted as having transmitted the ventral afferent arterial trunk is here considered as having housed the hepatic vein, which emptied into the venous sinus of the heart. The ventral afferent arterial trunk may thus have passed through the former «œsophageal ›› foramen.
The problem of the position of the dorsal nerves in the Osteostraci is discussed, and it is suggested that the three foremost nerve canals opening into the oralobranchial cavity housed the maxillary ramus of the trigeminus, the facial nerve and the glossopharyngeus nerve respectively. The mandibular ramus of the trigeminus must have accompanied one of the two foremost nerves, but for the moment it is impossible to decide which.
The problem of the nature of the interbranchial crests of the Osteostraci is briefly discussed. Comparison with the branchial apparatus of the Petromyzontida does not support the hypothesis that the interbranchial crests are part of the branchial arches, incorporated into the endoskeletal shield. A different hypothesis is proposed, that the branchial skeleton of the Osteostraci was situated entirely inside the oralobranchial cavity, and was attached to the endoskeletal shield only by the ventromedial processes. The grooves classically allotted to the efferent branchial arteries would thus have housed extrabranchial arteries, branching off from the dorsal aorta, and irrigating the ventral branchial musculature.
A phylogeny and a classification of the kiaeraspidians are proposed. The evolution of this monophyletic group is characterized by, e.g., reduction of cornual processes, shortening of the abdominal division of the shield, subdivision of the lateral fields, and enlargement of the supraoral fossae.
The phylogenetic position of the kiaeraspidians within the Osteostraci remains uncertain. Their sister-group may be either the benneviaspidiens or the thyestidians, or Thyestes alone (in which case they would have to be included within the thyestidians).