Fossils of the endangered sturgeons and peddlefishes are widely distributed. We here report for the first time the presence of one of the extinct osteichthyes genus Cylindracanthus (Liedy 1856a) from the Early Eocene lignite-bearing successions of the Kutch Basin, India. The present well preserved rostrum is characterised by numerous wedge-shaped components encircling the central canal that runs along its length, paired at the base and each wedge contributing to the formation of a ridge. The rostrum lacks teeth. The present find extends the palaeobiogeographical distribution of Cylindracanthus considerably and supports its Eocene age as dental remnants preserved in Cylindracanthus sp. shows a decrease in remanent dentition and tooth bases from the Cretaceous to the Eocene. Cylindracanthus is an useful palaeoenvironmental indicator as it has been found associated typically with deposits of nearshore marine environments. 

The late Cretaceous Auca Mahuevo nesting site (Neuquén Province, Argentina) has produced a large number of sauropod eggs, many of them containing the remains of embryos. Research at this site has generated important information about the development of the embryos, the morphology and eggshell microstructure of the eggs, and the reproductive behavior of sauropod dinosaurs. Cranial features present in the embryos have allowed their identification as those of titanosaurian sauropods. Differences in the texture of the sediments that contain some of the egg-clutches have illuminated their nest architecture. Microstructural studies of eggshells have expanded our knowledge of their variability and the incidence of pathologies within a reproductive titanosaurian population. Maps showing the spatial distribution of eggs and clutches. the stratigraphic distribution of the egg-beds, and the sedimentological context in which they are contained, have provided the basis for several inferences about the nesting behavior of these dinosaurs. 

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.
  

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). 

Abstract
 The validity of Propachynolophus Lemoine, 1891, supposedly an intermediate between Hyracotherium Owen, 1841 and Pachynolophus Pomel, 1847, has been questioned for a long time. A detailed analysis of features on which this genus is based further supported by a formal cladistic analysis demonstrates that Propachynolophus is not a valid taxon. The type species, “Propachynolophus gaudryi Lemoine, 1891” shall be assigned to Propalaeotherium Gervais, 1849, under the new combination Propalaeotherium gaudryi (Lemoine, 1891). “Pachynolophus maldani Lemoine, 1878”, later assigned to Propachynolophus, typifies the new genus Orolophus, under the binomen Orolophus maldani (Lemoine, 1878). The other referred species, “Propachynolophus levei Hooker, 1994” and “P. remyi Checa-Soler, 1997” are poorly documented, and both species shall be provisionally referred to as “Hyracotherium” levei (Hooker, 1994) and “Hyracotherium” remyi (Checa-Soler, 1997), pending new discoveries.
 
  

This paper proposes a systematic revision of the Oligocene Mongolian Ctenodactylidae, on the basis of abundant material obtained by screen/washing operations in stratified localities of the Ulantatal area (Inner Mongolia) (UTL1, 2, 3, 4, 5, 7, 6 & 8). A Chinese-German team has collected several thousands of isolated rodent teeth, and a number of fragmentary jaws. A new genus is identified (Alashania nov. gen. tengkoliensis nov. sp.), and eight former species are reevaluated, Karakoromys decessus, Tataromys sigmodon, T. minor, T. plicidens, Yindirtemys ulantatalensis, Y. bohlini, Y. deflexus, with several synonymies. A new Yindirtemys species is described: Y. shevyrevae nov. sp. and another one close to that: Y. aff. shevyrevae nov. sp. Four new species, which are rare in the localities, remain in open nomenclature because they are not well-represented. Yindirtemys differs from the other genera by the permanence of crescentic structures, while the other genera show a general reduction of the trigonoid area (= anterior valley). We define a range of size variation for each well documented population. Although the dental morphology shows a wide range of variation, given that transitional morphologies occur in a single locality, it is possible to provide a clear definition for most species. We show that dental patterns of the different genera can be derived from the pattern of Karakoromys. As a number of Tataromyinae have been determined in several localities from China, Kazakhstan and Mongolia, usually on the basis of scarce material, or surface collections, the present study would be used to re-evaluate their attribution inasmuch as the taxa are now placed in the Oligocene stratigraphy. The diversity of sizes and forms reflects the adaptive radiation of the family during the Oligocene, within a forested environment where the vegetation was probably abundant. 

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. 

A comparative bone histological study of the three known genera of the endemic European ornithopod dinosaur family, Rhabdodontidae, is presented here in an ontogenetic context. Investigated specimens were assigned to different ontogenetic stages based exclusively on the histological indicators of osteologic maturation during diametrical bone growth; an entirely size-independent method as opposed to most previous studies. Qualitative comparison of bone histology of corresponding ontogenetic stages and elements among the three valid rhabdodontid genera, Mochlodon, Zalmoxes, and Rhabdodon, revealed some consistent patterns. Genus specific histological differences within Rhabdodontidae are most expressed between Rhabdodon and the Mochlodon-Zalmoxes clade. These indicate a prolonged phase of fast growth and a less constrained cyclicity in the growth dynamics of Rhabdodon, as opposed to the slower and more regulated growth strategy reflected in the bones of Mochlodon and Zalmoxes. These genus specific differences are consistent with the phylogenetic interrelation of the genera and are most probably related to the pronounced differences in body size. However, when compared to other ornithopods, most detected histological features in rhabdodontids do not seem to reliably reflect either phylogenetic relations or body size. A notable common feature of all rhabdodontid genera irrespective of body size is the ontogenetically early onset of cyclical growth and secondary remodelling; a pattern that more resembles the condition found in derived ornithopods than that described in more basal taxa which are closer relatives of rhabdodontids. The recognition of taxon-specific histological patterns as well as patterns indicative of ecological and thereby functional traits clearly requires more accurate, preferably quantitative evaluations.   

An increasing fossil record of dinosaur eggs and eggshells allows putting ootaxa within a chronostratigraphic framework, in order to study their distribution pattern leading eventually to their use as biochronological markers. For these purposes, high-quality data exists in four major regions; North America, South America, Europe and Asia (Central Asia and India). Most of the highly diverse dinosaur egg record has been dated as Latest Cretaceous in age (Campanian-Maastrichtian), reaching the Cretaceous-Tertiary boundary closer than the dinosaur bone record. However, dating continental sections is problematic and need to be carefully verified, as it appears when comparing the European dinosaur eggshell record from two well-studied areas. Ootaxa distribution in both sides of the Pyrenees (Tremp and Aix basins) shows comparable oospecies successions, but different chronology. This disagreement probably indicates that one or both successions have a wrong chronostratigraphic calibration.  

This paper describes the first hexanchid tooth from the Tithonian (Late Jurassic) of New Zealand. For the moment, this tooth represents the earliest representative of the fossil genus Notidanodon in the world and one of the most ancient neoselachians in the Southern Hemisphere. Despite the perfect state of preservation of the unique tooth, the species is left in open nomenclature, pending the discovery of additional specimens. Few nominal species have been assigned to the genus Notidanodon. Four from Cretaceous deposits: N. antarcti Grande & Chatterjee, 1987, Notidanodon dentatus (Woodward, 1886), Notidanodon lanceolatus (Woodward, 1886), Notidanodon pectinatus (Agassiz, 1843) and only two from Paleocene: Notidanodon brotzeni Siverson, 1995, and Notidanodon loozi (Vincent, 1876). Considering the important morphological variations observed between some of these species, it seems obvious that the genus Notidanodon is not monophyletic and will need a revision in the future. 
  

A new species, Otonycteris rummeli nov. sp., is described from the Late Miocene site Gritsev (MN 9) in the Ukraine. Otonycteris rummeli nov. sp. differs from those of most vespertilionids, except recent Otonycteris, Antrozous and Early Miocene Karstala silva, in having a well-developed entocingulid at the foot of the trigonid valley in the lower molars. The morphological resemblance of Otonycteris, Antrozous and Karstala is apparently a case of convergence in the evolution of the Old and New Worlds bat faunas. From at least the Middle Miocene the range of Otonycteris distribution spread to the whole of Central Europe and such a situation continued during the whole Late Miocene. This indicates a more arid climate in Europe during the Upper Miocene compared to the Quaternary. The reduction of the distribution range of Otonycteris and its extinction in most of the territory of Europe could have been caused by the global climatic cooling and increasing glacial cycle amplitude during the onset of the Quaternary. 

The litoptem Proterotheriidae are extinct endemic South American ungulates frequently used as an example of evolutionary convergence with the horses. They were considered to be exclusively Tertiary representatives with the youngest record being in the late Pliocene, before the appearence of the equids and cervids during the Great American Interchange. Two undoubted Pleistocene records in Argentina and the specimen here described from Uruguay, confirm the persistence of the proterotherids into that period. In the Quaternary, these ungulates are found outside the typical pampean region and probably were confined to a few northern and warmer more forested relictual microhabitats.

  

The fossil mammals discovered in the quarry of Rians (Sparnacian, Provence) are described. Among these forms, Hyracotherium is interesting because of the little molarization of the lower premolars and its small size, and Diacodexis by its small size and very primitive astragalus ; they may be the most primitive representatives of their respective orders. Also, Proviverra eisenmanni n. sp. is the smallest and most primitive hyaenodontid yet described. Hyopsodus itinerans is the first species of this genus described France. Among other rare fossils is a new species of bat, a small palaeoryctid, and other forms not yet identified. Marsupials are varied. Several new species are present among the rodents. The fauna is well-balanced and rich in small hyopsodontid condylarths. It is stratigraphically situated at the
Dormaal reference-level, at the base of the early Eocene, and is considered equivalent to the late Clarkforkian of North America. The hypothesis is presented that new forms appearing at the beginning of the Wasatchian in North America migrated, in fact, at that time from Europe.

  

Bats are among the most numerous and widespread mammals today, but their fossil record is comparatively meagre and their early evolution poorly understood. Here we describe a new fossil bat from dental remains recovered from late Early Eocene sediments at Prémontré, northern France. This 50 million-year-old bat exhibits a mosaic of plesiomorphic and apomorphic dental features, including the presence of three lower premolars, a single-rooted p3, short p4 with metaconid, myotodont lower molars and a tall coronoid process of the dentary. This combination of features suggests it is an early member of Vespertilionidae, today’s most speciose and geographically widespread bat family. The Prémontré bat has bearing on hypotheses about the origins of vesper or evening bats (Family Vespertilionidae), as well as crown-group chiropterans.


  

A recently discovered, almost complete specimen of a hybodont tooth, allows us to describe as a new species, fairly common, but usually fragmentary teeth in the Navesink Formation of New Jersey: Hybodus novojerseyensis nov. sp.
Three additional taxa are also described : Heterodontus creamridgensis, Squalicorax sp. and Pseudocorax affinis which is noted for the first time in North America.
The whole elasmobranch fauna of the Early Maastrichtian localities of New Jersey is reevaluated and several generic assignments are changed in comparison to the list previously published in 1975 (Cappetta
& Case). 

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. 

Situated in the Cape region of the Republic of South Africa (RSA), the paleontological site of Langebaanweg is dated to 5.1 Myr and is famous for having yielded an abundant vertebrate assemblage, including numerous rodent species from the Mio-Pliocene transition. Based on molar morphology and skull anatomy, the single Gerbillinae taxon identified at Langebaanweg and described in this paper is allocated to Desmodillus, which is a modern monotypic South African endemic genus. It is significant in being the oldest representative of the genus in Africa. We describe here a new species of this genus which is larger than the modern D. auricularis, but nevertheless retains some of its main characteristics, namely the shape of the maxilla and mandible, the presence of poorly fused alternating cusps, and no longitudinal crest. This taxon differs from modern South African Gerbilliscus representatives in some mandibular and maxillary characters, in the m1 prelobe cusp, and in having less fused cusps. Two fossil Gerbillinae discovered in the Upper Miocene of Africa and Asia, Abudhabia and Protatera, have been compared with the new species. We discuss their relationships with modern and Plio-pleistocene Gerbillinae and conclude that Abudhabia could be the sister taxon of Desmodillus and that around 6-5 Myr a vicariance event allowed Gerbillinae to diversify into modern Desmodillus in South Africa, and Gerbilliscus in East Africa. The murine/gerbilline ratio, which is a good indicator of rainfall, supports other proxies which suggest that at 5.1 Myr the climate in the Langebaanweg region was more humid than today. 

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. 

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 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.