The late Pliocene site (MN 16) of Balaruc II (Hérault, France) has provided remains of the following amphibians and reptiles: Chelotriton pliocenicus nov. sp. and Triturus marmoratus (Salamandridae), cf. Rana (Ranidae), cf. Blanus (Amphisbaenidae), cf. Agama (Agamidae),  Gekkonidae indet., Lacerta s.l. (Lacertidae), "Ophisaurus" sp. (Anguidae), Michauxophis occitanus (Aniliidae), Erycinae indet. (Boidae), Elaphe cf. E. longissima and Malpolon sp. (Colubridae), cf. Naja (Elapidae) and Vipera sp. (Viperidae). The salamandrid Chelotriton pliocenicus and the aniliid Michauxophis occitanus constitute, up to now, the only records of these groups in the European Pliocene. The fauna is indicative of a warm, dry
subtropical climate. 

A fossil species of the extant genus Leuconoe, L. lavocati n. sp. from Le Garouillas Oligocene locality, Quercy phosphorites, SW-France, is established in nomenclatural standards. 

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. 

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. 

Le Mémoire Extraordinaire 1988 de PALAEOVERTEBRATA regroupe dix articles consacrés au gisement à mammifères du Miocène supérieur de Montredon (Hérault), connu et classique depuis la fin du siècle dernier, et auquel est lié le nom du savant paléontologue lyonnais Charles Depéret.
Cette monographie vient normalement à la suite de celle parue en 1982 dans PALAEOVERTEBRATA, dont les différents articles traitaient de la stratigraphie du gisement, et faisaient l'étude des différents groupes de micromammifères représentés dans la faune (insectivores, chiroptères, rongeurs). 

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). 

The first part of this study was devoted to a descriptive analysis of teeth morphologies among the vespertilionine bats. This leads now to a tentative synthesis, providing views on the systematics of the group. The results could be seen according to three distinct but closely related purposes : 1 - the sorting of the genera contents in order to conform the genera units to homogeneous taxa that could represent natural issues of evolutionary lineages ; 2 - the investigation of relationships between extant genera in order to infer the possibilities of common origin ; 3 - according to the preceeding items and to the observed evolutionary trends, a tentative phylogeny, modest and cautious. The contents of many genera are sorted : Leuconoe is removed from subgeneric to generic position, whereas Myotis becomes a subgenus of it ; the myotodont species are cleared away from the Pipistrellus genus ; Glischropus and Scotozous are synonymized within Pipistrellus ; Hypsugo is raised to the generic level ; some species previously ranged within Pipistrellus will form provisionally a collective group, Attalepharca nov. ; the Eptesicus genus is broken up, the excluded species being grouped within Nycterikaupius gen. nov. ; the Nycticeini tribe is defined again after exclusion of Otonycteris , Scotoecus, Scotophilus , and addition of Hesperoptenus ; the species la io and Pipistrellus tasmaniensis are removed to Eptesicus (n.s.) and Pipistrellus dormeri to Scotoecus. Groupings of genera are stated according to the main evolutionary trends of I1/. The relevance of these is often warranted by close morphologic similarities of other teeth. This leads to a recognition of the major evolutionary radiations which occurred in the group. The filiations schematized at the end of the work show the dental relationships observed between the extant genera, and could represent a phylogenic framework. Two major facts are to be underlined : 1- the early divergence of leuconoids ; 2 - the successives crossings to myotodonty from the nyctaloid flow. Fossil data from the literature are punctually and tentatively incorporated within phylogenic sketches. 

A well-preserved anterior cranium of Paranourosorex gigas RZEBIK-KOWALSKA, 1975 from Podlesice, Poland, provides additional knowledge of this rare shrew, including almost complete maxillary dentition. The systematic status of this species as a relative of recent Anourosorex MILNE-
EDWARDS, 1870 is confirmed 

Some fragmentary remains of spines and endoskeletal elements, referred here to as ctenacanthid like elasmobranchs, are recorded in the Middle Devonian of Bolivia. These specimens, and some others from the Eodevonian of Brasil represent the only  Devonian fish remains hitherto known from South America and indicate that further discoveries may be made in their original localities respectively.
  

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.
  

Messiphoca mauretanica nov. gen., nov. sp. représente le premier Phocidae fossile recensé en Afrique du Nord. Provenant du gisement sahélien (Miocène supérieur) de Raz-el-Aïn (Algérie), il est connu par quelques os du membre antérieur (humérus, radius, ulna), quelques vertèbres dorsales et un crâne très fragmentaire. La description de cette forme nouvelle amène à considérer Messiphoca mauretanica comme un Monachinae archaïque proche de l'origine du groupe Pliophoca - Monachus. L'incidence de cette interprétation d'un Phocidae «pré-Messinien ›› sur la crise de salinité du Messinien est aussi envisagée. 

Les mammifères post-glaciaires de Corse. Etude Archéozoologique, par Jean-Denis Vigne, 1988. XXVle suppléments à "Gallia Préhistoire". Editions du C.N.R.S., Paris, 337 p. FRF 300. ISSN 0072-0100, ISBN 2-222-04130-9. 

A lot of isolated teeth of a pteropodid fruit bat has been recently found within an assemblage of micromammals recovered from a karstic fissure filling named Lo Fournas-Il near the locality of Baixas (Pyrénées-Orientales, France). The fauna is Middle Miocene Serravallian age. The fossil fruit bat appears morphologically close to Rousettus; its size is that of a recent medium-sized fruit bat. While the fruit bats are very poorly known as fossils, this discovery shows that one of their recent types of dentitions was perfectly established by Middle Miocene times, and supports the presumed long geologic story of the suborder. One of the major invasions of the Old World fruit bats, supposed originated from SE Asia, reached up to Europe. A suborder unit is added to the miocene fauna of this continent. 

An upper giraffid premolar without any indication about its origin is preserved at the Montpellier University among numerous fossils from the ruscinian formation of Montpellier. It can be related to Samotherium, of the Upper Miocene in Eastern Europe, North Africa and Asia, or more probably to Bramatherium  or Hydaspitherium of the Pliocene of South East Asia. The sedimentological study of the matrix shows a calcareous background, which may indicate that this tooth does not come from the Montpellier formation. 

Two new Squalicorax species, S. benguerirensis nov. sp. and S. microserratus nov. sp. are described from the Lower Maastrichtian of the Benguérir phosphate open mine, Ganntour deposit, Morocco. The species S. benguerirensis nov. sp. was classically assigned to S. yangaensis since Arambourg (1952) and has been also recognized in coeval deposits from eastern USA to Mid-East. The species S. microserratus nov. sp. correspond to the lateral teeth of S. kaupi as reported by Arambourg (1952) and which is now referred in fact to S. bassanii. The comparison of these two new species with other Anacoracids, known in Moroccan or elsewhere, allows highlighting the great taxonomic and ecological diversities of this family during the Cretaceous.
  

Previous chronological arrangements of South American Quaternary land mammal faunas are appraised on the basis of current geological and paleontological data. Three South American late Pliocene-Pleistocene land mammal ages are conventionally recognized, from oldest to youngest, the Uquian, Ensenadan, and Lujanian ; all are defined on Argentine faunas.

     The Uquian is based fundamentally and historically on the fauna from the Uquía Formation in Jujuy Province, northwestern Argentina. Important known formations in Argentina yielding Uquian Age faunas include the sub-surface Puelche Formation (or Puelchense) near the city of Buenos Aires, and the Barranca de Los Lobos and Vorohué Formations between Mar del Plata and Miramar, Buenos Aires Province. A tentative subdivision is propos-ed for the Uquian into three subages based on knowledge of the Mar del Plata-Miramar sequence, from oldest to youngest, the Barrancalobian, Vorohuean, and Sanandresian. In Argentina the Uquian is presently marked by the first known record of Scelidodon, Hydrochoeropsis, Ctenomys, Canidae, Ursidae, Gomphotheriidae, Equidae, Tapiridae, Camelidae, Cervidae, and the last known record of Thylatheridium, Thylophorops, Dankomys, Eumysops, Pithanotomys, Eucoelophorus, Hegetotheriidae, Sparassocynidae, and Microtragulidae.

The Ensenadan Age is based on the fauna from the Ensenada Formation near the city of Ensenada, Buenos Aires Province. In Argentina the Ensenadan is marked by the first known record of Lomaphorus, Neothoracophorus, Plaxhaplous, Cavia, Lyncodon, Lutra, Galera, Smilodon, Dicotyles, Lama, Vicugna, the last known record of Orthomyctera, and the only known record of Brachynasua.

     Typícal beds of late Lujanian Age in Argentina consist of fluvial deposits occupying stream channels, and shallow basins, often incised into beds of early Lujanian (i.e. Bonaerian of early workers) and Ensenadan Age. The Lujanian Age is based on a fauna from beds along the Rio Luján, about 65 km west of the city of Buenos Aires, Buenos Aires Province. The Lujanian in Argentina is marked by the first record of Equus, Chlamyphorus, and Holochilus, and the last record of Megatherioidea, Glyptodontoidea, Arctodus (=Arctotherium), Smilodon, Litopterna, Notoungulata, Proboscidea, Equidae, Morenelaphus, and Palaeolama.

   These land mammal ages are often difficult to recognize in other South American countries. The compositions of South American Pleistocene faunas vary with the environment. Some taxa were widely distributed in fossil deposits throughout the continent, but their occurrences need not reflect synchroneity. This is a result of changing climates and habitats in time. Consequently, proposed intracontinental correlations need confirmation based on magnetostratigraphy and a radioisotope time scale. Paleontologic characterizations of these land mammal ages (i.e. first and last record, and guide fossils) are useful for much of Argentina, but extensions to most of the other parts of South America are at best tenuous.

The majority of known non-Argentine Pleistocene faunas are believed to be Lujanian in age. Possible non Argentine early Pleistocene (Uquian) faunas include Ayo Ayo and Anzaldo in Bolivia, and Cocha Verde in southern Columbia. A possible middle Pleistocene (Ensenadan or early Lujanian) fauna is the Chichense of Ecuador. Paleomagnetic and radioisotopic date (MacFadden et al., 1983) clearly indicate that the greater part of the Tarija fauna (Bolivia) is Ensenadan in age.

  The end of the Pleistocene and beginning of the Holocene in South America is marked by extinction of nearly all large mammalian herbivores and their specialized large predators. Radiocarbon age determinations suggest that large scale extinctions of megafauna occurred between 15,000 and 8,000 yrs. B.P. (years before present). 

The recently discovered, very rich, Pliocene locality of Layna (Soria, Spain), has already yielded 30 species of mammals. Hipparion fissurae, described here is more dolichopodic than other Hipparion. It is related to Hipparion crusafonti from Villaroya (Villafranchian), but more slender between other characters.
  

A strong lophodonty, an extreme heterodonty, some hypsodonty and regular overlayings of coronal cement are prominent features of the genus Leptolophus (Palaeotheriinae = Palaeotheriidae s.s.). The histological pattern of the teeth unusually joins type II enamel prisms, characteristic of advanced ungulates, together with archaic features, such as an almost complete lack of Hunter-Schreger zonation and a weak expanse of peritubular dentine. The skull is narrow and slender, with an elongated ante-orbital facial region, a moderately notched nasal aperture, a rather elongated post-canine diastem, parallel zygornatic arches and a fairly dorsally located squamoso-mandibular joint.The functional analysis brings to light "ectolophodont" masticatory cycles with two phases, in which maximum power was applied, contrary to equíds, on hindmost teeth; likewise, skull accomodations to increasing height of the teeth are quite different. This study leads to the assumption that Leptolophus may have been light mammals, living in rather open surroundings, browsing on herbaceous plants or leaves cropped close to the ground. Moreover, it appears that it could have been some inadequacy of dental structures to the dietary, which leaded to quick wear of the teeth and to many enamel notches, but had been somewhat balanced by the early increase of hypsodonty, not induced in such a case by a biotop deterioration (as it will happen at the end of the Eocene). This ínadaptation might account for the short duration of the genus Leptolophus, whose the 3 species, L. stehlini, L. nouletí and L. magnus n. sp. are indeed confined in the level MP 16. Its geographical spreading (as far as known, South of western Europe) and the morphological pattern of its dentition suggest that this genus would have been related to early upper Eocene endemic spanish forms.





  

The revision of the Rhombodontidae from the Maastrichtian of Morocco led us to the description of a new species: Rhombodus andriesi.

The biometrical study of populations of R. binkhorsti and R. microdon, species sometimes considered as synonymous, supports the conclusion that they represent two distinct species and not young and adult specimens of a single species. The stratigraphical range of these two species confirms this
result.

The reexarnination of type-series studied by C. Ararnbourg led us to revise the generic status of Rhombodus bondoni which is now ranged, because his dental features, in the new genus Dasyrhombodus showing a less derived dentition than Rhombodus. The stratigraphical range of each species is clarified within the phosphatic series. 

The Las Águilas site near Porvenir de Jalpa, Coahuila, Mexico, is extremely rich in tetrapod remains comprising both bones and trackways of several dinosaur taxa of late Campanian age. Within a 50 m thick section we identified at least nine layers with dinosaur bone assemblages. In one of these the dinosaur bones are associated with remnants of eusuchian crocodilians, turtles, plesiosaurs, pterosaurs, tyrannosaurids, dromaeosaurids, parksosaurid, hadrosaurids, ceratopsids, and ankylosaurs. This layer is also rich in coprolites of turtles, crocodilians and likely theropods, thus providing evidence for the wealth of Late Cretaceous vertebrate life in the area.