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. 

Is hereby described an impressive lchnoiauna belonging to the Lower to Middle Ludian of the Gard (S. France). The slab, already cleaned over a length of 18 m, is located near the top of the Potamides aporoschema lacustrine limestone (Lower Ludian, Euzet zone). It is therefore older than the Célas sandstone deposit, and still more than the Melanoides albigensis and M. acutus marly limestone corresponding to the Upper Levels of the Ludian stage. Although biostratigraphically older than the La Débruge and Montmartre zone, the biotope shows already a sampling of very tall Artiodactyles, Perissodactyles and Carnivorous. One of the most « majestic ›› Artiodactyles, Anopolotheriipus lavocati, nov., points out a huge size type. To mention also among the Ichnotypes described, 10, the big Perissodactyle Palaeotheriipus similimedius, nov., and the big Carnivorous Hyaenodontipus praedator, nov. 

Rodents first appear in the latest Paleocene or earliest Eocene as very fragmentary specimens (Family Paramyidae) known largely from a single locality. After this sparse beginning, rodents are usually abundant in the North American record if proper recovery methods are used. Utilization of rodents for biostratigraphic purposes depends on 1/ extinction, and 2/ replacement by evolution of endemic groups and/or incursions of Old World rodents, and rarely and late by South American kinds. These incursions are separated by relatively long periods of isolation in the Paleogene, but more episodic in the Neogene. At least 10 rodent zones can be characterized by major distinctions, and these zones can be amplified into as many as 16 with little trouble. In general, rodent genera permit as refined a zonation as do genera of large mammals. Distinction at a specific level has not been attempted herein except in the Blancan and Post-Blancan. 

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. 

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. 

The Squamates from Sainte-Néboule are charateristic of the Upper Eocene from the Phosphorites du Quercy. Most genera known from this locality do not survive the « Grande Coupure ». Cadurcoboa insolita gen. nov., sp. nov. is a small Boidae very characteristic of the Upper Eocene. 

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. 

Description, for the first time, of the skull of Ruscinomys Depéret on the basis of a nearly complete specimen, and description of a new facial part of a Megacricetodon Fahlbusch skull (material from upper Miocene, Spain). New description of the skull (facial part) of " Cricetodon" incertum Schlosser on the basis of the specimen from the Oligocene of Quercy phosphorites already published by S. Schaub.
Comparison of the skull of “ C. ” incertum with that of the asiatic genus Cricetops Matthew and Granger and that of the North-American Eumys Leidy. These three genera of similar age display very distinct characteristics; their common origin must go back to the Eocene, as Wood believed.
Comparisons of the auditory regions of Ruscínomys and of Megacricetodon where important differences are noted. Comparison of the Cricetodontines from European Miocene with contemporary Cricetines. Contrary of the opinion held by Schaub, their anatomical differences do not seem suflicient to warrant the contention that none of the Cricetines derive from a form close to one of the known Cricetodontines. 

The rodent-fauna (Cricetidae and Gliridae) recently found at Castell de Barbera (Spain) is similar to those from the other locslities of the Valles - Penedes - Can Ponsic 1 and Can Llobateres - : same composition and similar evolutionary level of the different species. On the other hand this fauna is different from those of Upper Vindobonian and Vallesian localities of the Calatayud - Teruel area. Castell de Barbera has an intermediate chronological position between the localities of Anwil (Switzerland) and Can Ponsic 1. It is still not possible to validate or invalidate the initial attribution based on absence of Hipparion of Castell de Barbera to the Upper Vindobonian. 

La faune d'artiodactyles de Ste-Néboule, qui comprend neuf espèces, présente de nombreux
points communs avec les faunes habituellement rattachées au Ludien supérieur, telles celles de La Débruge ou de Montmartre. A l'inverse de ces localités, on ne connaît pourtant, à Ste-Néboule, ni Oxacronae, ni Anoplotheriinae. Parmi les espèces du gisement se trouve une nouvelle espèce du genre Mouillacitherium (M. schlosseri n. sp.), cette forme devant être interprétée comme le dernier représentant du rameau. Nous faisons connaître par ailleurs la presque totalité de la denture du Dacrytherium saturninii, espèce qui était à ce jour très imparfaitement documentée. Ste-Néboule est, d'autre part, la seule localité où l'on peut signaler l'association probable de deux lignées du genre Amphimeryx. Les primates sont peu diversifiés à Ste-Néboule, puisque le groupe est limité au seul genre Adapis. Les genres Microchoerus et Pseudoloris, que l'on sait pourtant être représentés dans des gisements dâge voisin (Microchoerus ornatus à San Cugat de Gavadons et Mormont-Entreroches, Pseudoloris reguanti à San Cugat de Gavadons, Pseudoloris cf. reguanti à Neustadt ; cf. Louis et Sudre 1975) sont absents dans les faunes du Quercy de cette période. 

Based on isolated teeth two new scyliorhinid shark species, Scyliorhinus biformis nov. sp. and Scyliorhinus suelstorfensis nov. sp., are described from the Sülstorf Beds, early-middle Chattian, of Mecklenburg, northeastern Germany. They form part of a speciose assemblage of necto-benthic sharks and batoids which populated the warm-temperate to subtropical upper shelf sea of the south-eastern North Sea Basin. 

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

Fourteen distinct phyletical lineages which belong at least in three families: Ischyromyidae ALSTON, 1876, Gliridae THOMAS, 1896 and Theridomyidae ALSTON, 1876, have been identified after the study of more than 3600 rodent dental remains from about twenty Early and Middle Eocene european localities. A systematical and phylogenetical revision of these rodents has been achieved. Nearly all the specific and generic diagnosis are emended. Several new combinations and synonymies are proposed. Four new species and two new genera, Euromys nov. (Ailuravinae) and Hartenbergeromys nov. (Microparamyini), are named and described. Euromys nov. gen. is known by three distinctive ypresian (MP 7 to MP 10 european reference levels) chronospecies. This new lineage is thought to be the direct ancestor of Meldimys MICHAUX, 1968 and Ailuravus RUTIMEYER, 1891. A new species of the genus Plesiarctomys BRAVARD, 1850, Pl. lapicidinarum from Condé-en-Brie (MP 8-9 reference level), allows to relate the Plesiarctomys lineage to the Pseudoparamys MICHAUX, 1964 one. The taxa Sparnacomys HARTENBERGER, 1971, Pantrogna HARTENBERGER, 1971, and Corbarimys MARANDAT, 1989 are erected to genus rank; the last one is not thought to be an Ischyromyidae. A new chronospecies of Pantrogna, P. marandati nov. sp. from the locality of Prémontré (MP 10 reference level), is described. This lineage is at the origin of two others, namely Masillamys TOBIEN, 1954, including M. mattaueri (HARTENBERGER, 1975) nov. comb. (MP 10 reference level), and Hartenbergeromys nov. gen., known from MP 10 (H. hautefeuillei nov. sp.) and MP 11 (H. parvus TOBIEN, 1954) reference levels. The phylogenetical position of Hartenbergeromys nov. gen., at the origin of the european family Theridomyidae, is discussed. The systematical and phylogenetical status of two probable Paramyinae, "Paramys" woodi MICHAUX, 1964 and an unnamed genus and species, are discussed. New populations of the primitive Gliridae Eogliravus HARTENBERGER, 1971 and of the primitive Theridomyidae Protadelomys HARTENBERGER, 1968, are described and assigned to previously known species.

  

The study of another faunal assemblage (mostly macromammals) from Torralba de Ribota (Calatayud, Zara-
goza Prov.) demonstrates the Middle "Burdigalian" age of the deposit, MEIN zone 4a. Some ten genera have been recognized. a.o. Anchitherium, Aceratherium and Lagopsis. 

The rodents from the spanish locality of Can Ponsic 1 bring new data about some rodents species of the beginning of the Upper Miocene in South-West Europe. The criticims made by Mein and Freudenthal about the validity of the species Hispanomys thaleri from Can Llobateres are not justiíied. The study of the anatomy of the skull of Rotundomys from Can Ponsic 1 gives accurate information about the affinity of this genus with Cricetulus, and shows that the hypothesis, according to which Rotundomys is an ancestral form of the Arvicolids, is unlikely. The systematics of Heteroxerus and the phylogeny of the mio-pliocene Muscardinus species are also discussed. The Can Ponsic 1 locality is a little older than Can Llobateres.

  

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). 

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.

  

The middle Palaeocene of São José de Itaboraí (State of Rio de Janeiro, Brazil) has yielded a very rich and diverse snake fauna which includes Madtsoiidae, Aniliidae s.l., Boidae, Tropidophiidae s.l., Booidea incertae sedis, and Russellophiidae. The present article (part I) deals with Madtsoiidae and Aniliidae s.l. Madtsoiidae are represented by many vertebrae and a few skull bones. They comprise one new species assigned to the genus Madtsoia (M. camposi sp. nov.). However, the definition of the genus Madtsoia is unsatisfactory and the generic allocation might be provisional. A few elements, vertebrae only, belong to the Aniliidae s. l. Two taxa are referred to this latter group: Coniophis cf. C. precedens and Hoffstetterella brasiliensis gen. et sp. nov. The forthcoming part II will deal with Boidae.

  

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

The 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.