We experimentally explore the early taphonomic stages involving the decay and biodegradation of buried eggs and eggshells. Unfertilised commercial chicken eggs and eggshell fragments were buried in plastic containers and were kept under controlled conditions for eight months. Half of the containers were filled with marl, and the remainder with sand. All were saturated with fresh tap water, acidified water, sulphate water, or seawater. They were kept in the dark at 23.4-26 °C, except one, which was kept in a heating chamber at 37.4°C. We expected that different burial conditions would produce distinct taphonomic outcomes. Instead, the taphonomic alterations of buried eggs parallel that of the alteration of egg proteins (i.e., denaturation and/or putrefaction) with an additional role played by the eggshell. Mummification, encrustation, distortion and fragmentation, and necrokynesis (vertical displacement) depend on organic matter decay. The experiment identifies environmental conditions that may favour or actively promote these taphonomic processes. Of these, early pyritization is one of the most relevant. For comparative purposes, samples of fossil and extinct eggshell representing three distinct environmental burial conditions were examined. These included Megaloolithus, Caiman crocodilus, and Struthio camelus ootypes. The geochemical analysis of these eggshells showed no significant differences among the chemical variables of these fossil and extant ootypes. Eggshells exhibited a stable composition over a range of experimental conditions. 
  

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.

  

Enamel microstructure in the incisors of Old- and New World hystricognath rodents:

The incisor enamel microstructure in more than 100 genera of fossil and Recent hystricognath and sciurognath rodents was studied. A multiserial schmelzmuster is present in the Hystricognathi, the Ctenodactylidae, advanced Chapattimyidae, and in Pedetes. A redefinition of pauciserial and multiserial HSB is given that makes the two enamel types unambiguously distinguishable which apparently represent well defined evolutionary levels. In the pauciserial Schmelzmuster the IPM is thicker than in the multiserial one. In pauciserial HSB the IPM always surrounds each prism, and the crystallites of the IPM run parallel to prism direction; transition zones between HSB are lacking; the inclination of the HSB is normally very low and the prism cross sections are not flattened but somewhat irregular. The number of prisms per HSB is no good distinctive character for pauciserial and multiserial HSB, since there exists a wide overlap. The pauciserial schmelzmuster is primitive, the multiseiial derived because: 1. the pauciseiial schmelzmuster appears earlier in the fossil record in the most primitive rodents (Paramyids s.l. and Ctenodactyloids); 2. the Eocene Ctenodactyloidea show pauciserial HSB but the Oligocene and younger ones are characterized by multiserial HSB; 3. in the outgroup comparison, the Eurymylidae (Mixodontia) show pauciserial HSB; 4. biomechanically, multiserial HSB strenghten the enamel better than pauciserial HSB, since their IPM runs nearly always in an angle of 45° or more to the prisms.

In multiseríal HSB three subtypes can be distinguished which are differentiated by the IPM orientation. Primitive is a (rarely strict) parallel or acute angular, anastomozing IPM, and derived is an interrow sheet-like ("plattenartige") IPM. This evolutionary polarity is indicated by enamel evolution in the Ctenodactylidae which show an acute angular IPM in the Oligocene and a rectangular interrow sheet-like IPM since the Miocene. Among the Caviomorpha a rectangular interrow sheet-like IPM is restricted to the Octodontoidea; therefore they must be considered derived in terms of their enamel structure. The first multiserial HSB in rodent incisors appear in phiomyids or chapatrimyids from the Upper Eocene of Algeria. The IPM is acute angular and anastomozing. The worldwide next younger multiserial HSB are found in Lower Oligocene phiomyids of Fayum, Egypt There already a rectangular interrow sheet like IPM is present (in Metaphiomys) besides the acute angular anastomozing IPM.

The first Caviomorpha from the Deseadan (Oligocene-Miocene) likewise show already acute angular anastomozing IPM (e.g. Scozamys) and rectangular interrow sheet-like IPM (Platypittamys). Therefore the first Caviomorpha cannot be positioned close to a transition from pauciserial to multiserial HSB. In none of the potential caviomorph ancestors from southern North America multiserial HSB or transitional stage between pauciserial and multiserial HSB could be found. The similarities between the enamel types of the Fayum rodents and the rodents from the Deseadan of South America make a derivation of the Caviomorpha from Paleogene North African phiomorph rodents or their direct ancestors most probable. This supports at the same time a descent of the platyrrhine Primates from North African anthropoids.
  

The dentitions as well as one complete and several partial skeletons of Equoids from the Eocene lignite beds of the Geiseltal locality are revised. Instead of 13 species distinguished up to now 3 chronoclines with 5 species and 3 separate species are recognized (text. fig. 1). Propalaeotherium hassiacum HAUPT, 1925 is evolving into Propalaeotherium isselanum (CUVIER, 1824) between the levels of the « obere Unterkohle ›› and the « untere Mittelkohle ›› of the Geiseltal section. Propalaeotherium argentonicum GERVAIS, 1849 is shown to be present in the « untere Unterkohle ››, whereas Lophiotherium pygmaeum (DEPERET,1901) occurs in the « obere Mittelkohle ›› and in the « oberes Hauptmittel ››. Plagiolophus cartieri STEHLIN, 1904 appears during the transition from the « Mittelkohle ›› into the « Oberkohle ›› as the earliest true Palaeothere. Therefore the « Oberkohle ›› is already regarded as Upper Eocene. This is corroborated by the occurrence of a phyletic descendant of Propalaeatherium parvulum (Propalaeotherium n.sp.) in the middle and upper "Oberkohle " because this species appears otherwise for the first time at the mammal level of Lissieu. On the other hand Propachynolophus gaudryz (LEMOINE, 1878) described by Matthes (1977) from the « untere Unterkohle ›› turns out te be in fact a Phenacodont. Thus the decisive argument for classifying the « untere Unterkohle ›› as Lower Eocene has to be dropped. Biostratigraphically the « Unterkohle ›› and the «Basishauptrnittel ›› correspond with the lower Middle Eocene (mammal level of Messel), whereas the «unteres Hauptmittel ›› and the « untere Mittelkohle ›› are equivalent to the middle part of the middle Eocene (mammal level of lssel), and the « obere Mittelkohle ›› together with the « oberes Hauptmittel ›› coincide with the upper Middle Eocene (mammal level of Bouxwiller). 

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 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 Tertiary of the Salla-Luribay basin consists of red beds affected by the second period of the andine compression, of Miocene ending age. The Tertiary layers are exposed at an approximate elevation of 3.500 to 4.000 meters. Two stratigraphic units can be distinguished in them: the Luribay conglomerates, in which vertical clifts result from erosion, and the Salla layers consisting mostly of consolidated clays. These clays are very fossiliferous and have furnished a rich vertebrate fauna which gave to R. Hoffstetter the possibility to establish the Oligocene age of these beds. Sediments of same age has been reported to be present in several other places of Bolivia, particularly near Lacayani, where have been collected highly hypsodont Rodents, different from those found in Salla-Luribay basin. 

In recent years, the techniques of chemical preparing have permitted a rich paleontologic material to be obtained from the phosporitic sediment of Bouzigues (Hérault, France). The fauna of this locality is comprised of quite varied microvertebrates, amphibians, reptiles, birds, mammals. Twenty five species of the latter, belonging to seven orders, are today known from the site. Among them, the numerous rodents have allowed L. Thaler to chronologically situate this fauna in the Zone of Laugnac (<< late Aquitanian ›> of some authors).
The chiropterans are, with the rodents, the best represented of the locality's mammals. Three families comprise the bat fauna, with nearly complete dominance by one of them (Hippoxideridae) over the two others (Megadermatidae and Vespertílionidae)
Six forms are described, of which three are new species and one a new sub-genus.
Megaderma braillomi n. sp., an animal of rather large size, shows like the Miocene megaderms several evolved dental characters, translating the adaptation of these animals to a partially carnivorous regime. The Bouzigues species seems, however, to represent a particular lineage.
Hipposideros (Brachipposideros n. subgen.) dechaseauxi n. sp. and Hípposideros (Brachipposideros) cf. collongenris Depéret, small sized forms, belong to a group rather well represented in the late Oligocene and early Miocene of Europe, and not distinguished until now within the genus Hipposideros.
Hipposideros (Pseudorhinolophus) bouziguensis n. sp., is the most abundant mammal in the locality and, occuring at the Oligocene-Miocene limit, the last representative known of the subgenus Pseudorhínolophus, common in Europe from the middle Eocene.
However, beyond Neogene and Quaternary times, certain among the numerous living species of Hipposideros are close to Pseudorhinolophus and others to Brachipposíderos. 'This fact would in the future justify a global revision of the genus, on the basis of comparative anatomy of the squeleton and of the teeth.
The bat fauna of Bouzigues is completed by two small Vespertilionidae, rare forms, Myoris sp. I and sp. II.
  

The Tafna Basin corresponds to the lowlands, which are located in front of Tessala and Traras ranges, below the Tlemcen mountains, Algeria. This basin displays a complete sedimentary cycle dominated by lagoonal-fluvial and marine deposits. The continental formations located at the base of these deposits are mainly composed of alternating sandstones and clays. An early late Miocene age has been previously attributed to them, based on direct correlations with marine deposits. Search for micromammal fossils led to the discovery of three different rodent species from a single level of the Djebel Guetaf section, located at the bottom of these deposits. The rodent assemblage indicates a late Miocene age. Combined magnetostratigraphical and biostratigraphical investigations were carried out to provide a more accurate age control of these continental deposits. Sixty-four oriented rock samples were collected for a magnetostratigraphic study along a 92 meters thick section including the fossiliferous layer. Rock magnetic investigations indicate the presence of both high and low coercivity minerals. Specimens subjected to progressive thermal demagnetization procedures show that the samples exhibit a high temperature magnetization component and display a normal polarity. Based on biostratigraphic constraints, the Guetaf section is correlated with Chron C4An, indicating an age ranging from
9.1 to 8.7 Myr.
  

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.
  

We present here the preliminary results from a new nesting site "Sextius-Mirabeau", discovered close to the historical centre of Aix-en-Provence in Upper Cretaceous deposits. This extensive megaloolithid nesting ground, the first large scale excavation (3225 m²) in France, yielded more than 530 eggs, some organized in clusters. Their study reveals the reproductive strategy of the megaloolithid egglayer group which indicates nesting fidelity and gregarious behaviour.  

Abundant crocodilian fossil remains have been collected, mainly by R. Lavocat. from several levels of the
Palaeogene of the Tilemsi valley (eastern Mali). Several dyrosaurids occur in the Palaeocene (Montian ?) : Phosphatosaurus sp., Hyposaurus bequaerti (Dollo). H. wilsoni (Swinton). H. nopesai (Swinton), Rhabdognathus rarus Swinton, R. compressus n. sp. ln the lower Eocene has been found a dyrosaurid which cannot be accurutely determined.In the middle Eocene were found a dyrosaurid, Tilemsisuchus lavocati n. g., n. sp., and an indeterminate eusuchian. 

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. 

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 eggshell of Nicobar scrubfowl (Megapodius nicobariensis) is described for the first time. Its egg porosity is calculated and discussed with data from several taxa (another megapode, some extant and fossil reptiles including a titanosaur group) in order to compare incubation types with eggshell structure. Eggshell microstructure reflects first phylogenetic traits and does not seem to have developed major adaptative features due to the incubation conditions, except for the pore canals. 

This paper is mainly devoted to the systematics of rodents from two middle Eocene (Bartonian) localities: Chéry-Chartreuve and Rocourt-Saint-Martin (Aisne, Eastern Paris Basin). These two localities are stratigraphically located slightly above the Auversian sands. The two faunas, which comprise 11 and 8 taxa, respectively, are very different in their composition. That of Rocourt-Saint-Martin shows strong similarities with that of the geographically very close locality of Grisolles, referred to the MP16 mammalian Reference level. The very distinct fauna of Chéry-Chartreuve includes a new species of Ailuravinae, Ailuravus nov.sp, and some teeth of the theridomyid Protadelomys, which represent archaic elements in the fauna. The most abundant species of the locality represents a new genus of primitive Theridomyidae. The presence of some teeth belonging to a new species of large Remyinae, Remys nov. sp., of Elfomys engesseri HOOKER & WEIDMANN, and a population of small dimensions referred to the genus Estellomys allow a correlation with Les Alleveys (Switzerland), with however some differences that would indicate an older age for Chéry-Chartreuve. Situated at the base of the "Marinesian" from the Bassin de Paris, this fauna is unquestionably different from those referred to the MP16 reference level and could represent an older level for which the macrofauna remains very poorly known. Conversely, the comparison of rodents from La Livinière II with those present in MP16 faunas, especially those of Robiac (Gard), shows a great similarity between both localities. This casts doubts on whether to keep this La Livinière II faunule to define the current MP15 reference level, while the biostratigraphical position of Pontils 26 (Spain), previously referred to this level, is reconsidered. Chery Chartreuse could be a good candidate for a new definition of the MP15 reference level. 

The exploitation of new early Eocene localities in the Paris Basin has resulted in the collecting of  numerous mammalian remains, among which are about 300 isolated teeth representing the rodents. They belong, for the most part, to the paramyid group. Only the latest level of the early Eocene has yielded rodents belonging to the pseudosciurid group. The paramyids, the object of this study, are represented by at least 5 genera and 10 species; they are distributed among 4 clearly dilferentiated subfamilies : Paramyinae Simpson 1945, Pseudoparamyinae Michaux 1964, Ailuraviínae n. subf., Microparamyinae Wood1962.
It results from this study that the principal types of rodents in the middle and late Eocene of Europe are clearly related to the forms described here: Plesiarctomys Bravard 1850 is related to Pseudoparamys Michaux 1964, Ailuravus Rütimeyer1891 to Meldimys n. gen., Gliravus hammeli Thaler 1966 to Microparamys nanus (Theilard1927), and some Masillamys Tobien 1954 to Microparamys russelli Michaux 1964 and to M. sp. 1. Gliravus and Masillamys are the oldest representatives of the Gliridae and the Pseudosciurídae, respectively, families which will progressively replace the Paramyidae in the course of the middle and late Eocene.
Two stages can be recognized in the history of te European Paramyidae fauna during the course of the early Eocene: the older is characterized by the Mutigny fauna, the younger by the Cuis fauna.
The Mutigny fauna appears already rather diversified and does not completely correspond, point by point, to the homologous fauna of North America. A geographic differentiation seems to have been manifested rapidly, unless the fauna established in Europe was already a little different from that which established itself in North America. 

Stratigraphic studies in the Aktau Mountains bordering the Dzhungarian Alatau Range in southeastern Kazakhstan have included mapping of Tertiary lithostratigraphic units, documentation of fossiliferous deposits, correlation of sections, etc. These investigations have led in turn to revised interpretation of the Tertiary geology of the area. The Tertiary sequence in the Aktau Mountains is represented by three lithostratigraphic units (in ascending order): (1) the middle Eocene Akbulak Formation; (2) the Oligocene Aktau Formation with a lower member including white quartz sands that contain fossil mammals, and an upper member including red-colored clays and sandstones, brick red clays, an anhydrite and gypsum clayey horizon, and bright brown-red clays; and (3) the upper Oligocene-Miocene Chul'adyr Formation with a lower member of greenish and yellowish conglomerates and gritstones, a middle member including grayish and yellowish sands and gritstones, and an upper member including brown and red clays and carbonate- and anhydrite-rich clays. The Aktau and Chul”adyr Formations represent separate cycles of sedimentation. Mammalian biostratigraphy and biochronology of the three vertebrate faunas in Aktau Mountains are reviewed. The mammalian fauna from white sands of the lower Aktau Formation is small but includes Ardynia and is thought to be early Oligocene in age. The mammalian fauna from conglomerates and gritstones of the lower member of the Chul”adyr Formation is also small but includes Paraceratherium and is thought to be late Oligocene in age. The mammalian fauna from sands of the middle member of the Chul'adyr Formation is extensive, with micro- and macrofauna attributed to Neogene mammal zones MN4 to MN 6, indicating a latest early Miocene to earliest middle Miocene age (Orleanian-Astaracian). Most genera of middle Chul”adyr mammals are known from the middle Miocene Shanwang faunas of China and from the Castelnau-d”Arbieu faunal assemblage (MN4-MN6) of southwestern France. 

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 recent excavation of the Upper Miocene locality of Montredon (Hérault) provides a rich material of Mammals. The present study deals with rodents. The new quarry is 10 meters above the classical Depéret's Quarry. No differences have been noticed between the rodent populations coming grom these two sites. The description of two new species : Hispanomys mediterraneus and Muscardinus heintzi is given and the dormouse Eliomys is recorded there for the first time. The new zonation of the Miocene given by Aguilar (1982) and the previously established correlations between marine and continental chronological scales give Tortonien age (estimated between 9 and 10 M.Y. old) to the site of Montredon, which belongs to the Mammal zone D 2.