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. 

An isolated right costal 1 from the Late Cretaceous Massecaps locality (Cruzy, Hérault, southern France) is assigned to Dortoka vasconica (Dortokidae). This find adds a new element to the Late Cretaceous turtle fauna of Cruzy and further supports the hypothesis that two distinct lineages of Dortokidae were present in Europe during the Late Cretaceous-Paleogene due to geographical isolation.
  

Near "la Lieude", in the Lodève basin, more than a thousand of footprints are distributed in a twenty of trackways which amounts to 220 m length. They have been found on calcareous siltstone level in the B site named also "Réserve Naturelle Volontaire". This last is located in the Saxonian summit dated Upper Permian. "La Lieude" tracks are described by using statistical methods then they are compared with others from the world Permian. What allows to distinguish 4 following ichnotaxa: Lunaepes ollierorum nov.ichnosp., Merifontichnus thalerius nov. ichnogen. and nov. ichnosp., Planipes brachydactylus nov.ichnosp. and Brontopus circagiganteus nov. ichnosp. All these traces are attributed with possibility or probability to Therapsida or to Therosauria, except Brontopus circagiganteus nov. ichnosp. that could be due to Caseamorpha. All these animals whose sizes have been estimated between l and 5 m lived probably in a playa environment.The biological and sedimentological data from "la Lieude" footprints levels compared with informations provided by the tracks orientations, suggest the following scenario. Animals coming from the North have crossed a sandy channel bank with plants zones by directing to the South for the majority. Maybe, they were going to the lacustrine part of the playa, close to "la Lieude" footprints that they have just trampled on. 

A new carcharhinid shark species, Physogaleus hemmooriensis sp. nov., is described from the Lower Hemmoorian (Behrendorfian, late Burdigalian, early Miocene) of Werder, Lower Saxony, Germany. P. hemmooriensis also occurs in the Edegem and Antwerpen Sands Members of the Berchem Formation, Belgium, and in the Miste Bed, Aalten Member of the Breda Formation, The Netherlands, which have an early to middle Miocene age. In the Western Atlantic region, the taxon is present in the early Miocene Calvert Formation of Delaware, U.S.A, which is largely contemporaneous with the Hemmoorian. 

Two incomplete pelves of the giant bird Gargantuavis philoinos are described from Late Cretaceous deposits at Fox-Amphoux (Var, south-eastern France). They consist of synsacra with attached parts of the ilia. One of them has undergone considerable dorsoventral compression, which makes it very similar in appearance to the holotype pelvis of Gargantuavis philoinos from Campagne-sur-Aude (Aude, southern France). The second specimen has suffered some lateral distortion but is uncrushed dorsoventrally. Because of this, its avians characters (including an arched synsacrum and widespread pneumatisation) are especially clear. These new specimens confirm the avian nature of Gargantuavis and reveal new details about its pelvic anatomy, but provide little new evidence about its systematic position within Aves. The geographical distribution and general rarity of Gargantuavis are discussed.
  

The East African Miocene Macroscelidea, lnsectivora and Chiroptera are revised on the basis of new material. New taxa proposed are: Miorhynchocyon, .n. gen. (Macroscelididae): Míorhynchocyon meswae, n. sp.: Pronasílío ternanensis. n. gen.. n. sp. (Macroscelididae); Hiwegicyon juvenalis, n. gen. n. sp. (Macroscelididae); Parageogale, n. gen. (Tenrecidae): Prochrysochlorinae, n. subfam. (Chrysochloridae): Propottininae, n. subfam, (Pteropodidae); Chamtwaria pickfordi, n. gen., n. sp. (Vespertilionidae). Gymnurechnínus songhorensis is synonymised with G. camptolophus. The new material provides additional information on the dentition, especially of Myohyrax oswaldi. Galerix africanus. Amphechínus rusingensis, Protenrec tricuspis and Parageogale aletris. Partial skulls are described of Amphechinus rusingensis, Protenrec tricuspis, Prochrysochloris míocaenicus and Taphozous incognita. The oldest member of the Macroscelidinae (Pronasilio) is described from Fort Ternan. Galerix africanus is closely related to G. exilis from Europe. Amphechinus rusingenesis is compared with Asiatic Oligocene Erinaceinae. The Miocene age of Crocidura is rejected. On the evidence of humeri, the following families of Chiroptera are newly reported: Pteropodidae, Nycterididae, Vespertilionidae, Molossidae. Propotto is regarded as an offshoot from the Pteropodidae, not ancestral to modern forms. Chamtwaria is a primitive vespertilionoid, provisionally placed in the Kerivoulinae. Erinaceidae probably entered Africa at the beginning of the Miocene, before 20 Ma. Faunistic differences between deposits are largely to be ascribed to differences in local environment. 

Comparison of various measurements of taxonomic evolution using stratigraphic range data for orders, families and genera of land mammals indicates several means by which deficiencies of the South American fossil record (e.g., presence of hiatuses, unequal temporal and geographic representation of ages, unequal systematic treatment) may be normalized, thus permitting a less distorted appreciation of diversity pattern and trend. Initial radiation of native taxa resulted in a relative equilibrium by early Eocene time. Subsequent increases in absolute diversity were apparently induced by immigration at the family level and by environmental factors at the generic level. Miocene through Pleistocene phases of faunal stability, herein characterized as chronofaunas, are punctuated by rapid turnover events resulting from a complex of factors, including adaptive radiation of immigrant taxa into unoccupied eco-space; environmental and concomitant habitat change induced by orogenic events of the Andes; and biotic interactions between native and immigrant taxa, including competition and prey naivete. The first two factors account for major faunal transitions in the South American middle and late Tertiary; immigration-induced turnover may have been of greater importance in shaping the character of the fauna upon the Great American Interchange and the arrival of man in the Neotropics 

The Late Triassic locality of Saint-Nicolas-de-Port (Meurthe-et-Moselle, France) has yielded numerous isolated teeth belonging to archosauriform reptiles. The following tooth groups can be identified: heterodont phytosaurs, the pterosaur Eudimorphodon, the prosauropod dinosaur Plateosaurus, three types of putative ornithischian teeth and 13 types of carnivorous Archosauriformes indet. Apparent venom-conducting teeth belonging to a new taxon of ?Archosauriformes (Graoullyodon hacheti nov. gen. nov. sp.) are also described. From a palaeogeographical point of view, the ornithischian teeth from Saint-Nicolas-de-Port (if their attribution is confirmed) are the oldest fossils of this group in Europe. The biostratigraphic distribution of the tooth forms mostly suggests a Late Norian or Early Rhaetian (depending on current interpretations) age of the deposits, but do not provide more precisions than fossils previously described from the area. The dietary habits and, consequently, the palaeoecological relationships of the different vertebrate groups discovered at Saint-Nicolas-de-Port are tentatively established: the ornithischian and prosauropod teeth reflect a herbivorous diet, whereas the other archosauriform teeth are probably from camivores or omnivores.

  

A cheek tooth recently unearthed in the Lopar Sandstone unit, of late Eocene age, in the northern part of Rab Island, Croatia, is one of the very few Eocene mammalian remains found in the Adriatic area. Thorough comparison of this tooth with those of Old-World Palaeogene mammalian orders suggests that it is a M3 belonging to an embrithopod afrothere. The specimen is referred to as Palaeoamasia sp. This genus was formerly known only in Eocene deposits of Anatolia but with close relatives in Romania among Palaeoamasiinae. The geographical distribution of this subfamily perfectly matches the recently-named Balkanatolian landmass, which experienced in-situ evolution of endemic mammals prior to the Grande Coupure event that occurred around the Eocene–Oligocene transition. This last event is characterised by massive Asian immigration in Western Europe and the supposed extinction of many endemic Central and Western European mammals, including Palaeoamasiinae.
  

In 2002, Antunes & Cappetta published several new taxa (genera and species) in a paper on Cretaceous elasmobranch faunas from Angola. One of the new genera was named Angolaia (Rajiformes, Hypsobatidae; type-species: Angolaia benguelaensis Antunes & Cappetta, 2002, Late Campanian/Early Maastrichtian of Angola). Recently, Dr. Christian Kammerer kindly informed us that the genus Angolaia was preoccupied by a cicadellid homoptere (Insecta), published by Linnavuori & Al-Ne'amy, 1983. So, according to mIes of the International Code of Zoological Nomenclature (ICZN 1999, articles 52, 60) this name became unavailable. Consequently, the Rajiformes genus Angolaia is a junior homonym, invalid and must be rejected. In replacement, we propose the new name Angolabatis. 

Macrauchenia patachonica was among the largest litopterns. It had a long neck with elongated cervical vertebrae, unique among endemic South American ungulates. We calculated the pattern of stress in the joints between the vertebral centra along the neck of the recently-extinct litoptern mammal M. patachonica for various hypothetical neck postures to determine which one is optimal. We also determined the zygapophyseal alignment positions for the neck, assuming a wide range of values for the thickness of the intervertebral discs. We concluded that a vertical posture is the one that best meets the requirements of nearly constant stress. This upright posture was probably a frequently adopted posture by M. patachonica while feeding or standing. It is also possible that occasionally it could adopt a gerenuk-like posture. In almost any other position, the standard deviations of stress values (SD) divided by mean stress (MS) have values between 0.4 and 0.5. Since it was a mixed feeder, M. patachonica probably used different postures to reach resources at different heights. However, an almost horizontal posture was required for the optimal articulation of the neck vertebrae. It probably represents the posture during fast locomotion, as suggested in a previous biomechanical study of locomotion. 

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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.  

Six orders of birds adapted to aquatic life are represented among the numerous avifauna of "Saint-Gérand-le-Puy": Gaviiformes, Procellariiformes, Pelecaniformes, Ciconiiformes, Phoenicopteriformes, and Anseriformes. The present study of this avifauna proposes several changes in systematics:- Procellariiformes: Puffinus arvernensis does not belong in Procellariidae but in Diomodeidae, and it is transferred to the fossil genus Plotornis previously described in the Middle Miocene of France. - Pelecaniformes: Phalacrocorax littoralis remains in Phalacrocoracidae; P. míocaenus is different from the modern species, and is transferred to the new genus Nectornis. Empheresula arvernensis, described in the Oligocene deposits of Gannat, seems to be present in Saint-Gérand-le-Puy too. Pelecanus gracilis shows many differences from the modern species, and belongs to the new genus Miopelecanus, - Ciconiiformes: Ardea formosa nom. oblit. is a synonym of Proardeola walkeri. - Anseriformes: a new species closely related to swans is described, and belongs to the fossil genus Cygnopterus, of the Middle Oligocene of Europe; this species is called C. alphonsi. The ecology of each species is suggested by comparison with that of its nearest living relatives, and by study of osteological adaptations. 

Palaeotis weigelti, from the Middle Eocene of central Europe, is a flightless, paleognathous bird. It appears to be a member of the ostrich lineage on the basis of trivial derived characters. It is a very primitive ratite, however, and does not possess any of the highly specialized cursorial adaptations that characterize the modern steppe -and savanna- dwelling ostriches. 

We report the discovery of amniotic eggshells and theropod teeth from the Late Cretaccous  period in Morocco.The megaloolithid family represents the only known dinosaur egg remains in the north part of Africa and attests indirectly to the occurrence of sauropod dinosaurs (titanosaurids) in the Maastrichtian of Africa.

  

Until the discovery of dinosaur eggshells locality in the Oukdiksou syncline, (Middle Atlas, Morocco) in 1999 (Garcia et al. this volume) the maastrichtian reptiles faunas were unknown in North Africa. Additional material from Achlouj-2 allows us to describe five oospecies, belonging to four oofamilies. The Megaloolithidae is recorded by Megaloolithus maghrebiellsis Garcia el al. and Pseudomegaloolithus atlasi oogen. novo oospec. nov. Tipoolithus achloujensis Garcia et al. is questionably considered as a Subtiliolithidae. A relatively small Elongatoloolithidae is represented by Rodolphoolithus arioul oogen. nov. oospec. nov. A thin Prismatoolithidae is described as a new oospecies of ? Pseudogeckoolithus Vianey-Liaud & Lopez-Martinez, 1997: P. tirboulensis. The diversity of these oospecies indicates that the dinosaur fauna comprises at least five dinosaur oospecies, with perhaps one sauropod and three theropods. 

The principles and practices employed in establishment and recognition of South American land mammal ages are reviewed along with previous and present concepts of distinguishing time, rock, and faunal units. Previous chronological arrangements of South American Tertiary land mammal faunas are appraised on the basis of recent geological and paleontological data. Twelve South American Tertiary land mammal ages are here recognized [from oldest to youngest, Riochican (middle to late Paleocene); Casamayoran (early Eocene); Mustersan (middle Eocene); Divisaderan (late Eocene); Deseadan (early [to middle?] Oligocene); Colhuehuapian (late Oligocene); Santacrucian (early Miocene); Friasan (middle Miocene); Chasicoan (late Miocene); Huayquerian (latest Miocene); Montehermosan (early to middle Pliocene); and Chapadmalalan (late Pliocene)]. As all except the Friasian were originally defined on the basis of Argentine faunas, these are discussed first and at length, and each is reviewed with discussion of type locality, stratigraphy, type fauna, and faunal correlations. Non-Argentine faunas are then discussed country by country in alphabetical order.

     A review is given of radioisotope dates obtained on volcanic rocks (i.e., basalts, tuffs) associated with mammalbearing beds in Argentina. Based on these age determinations and on correlation of the late Tertiary land mammals involved in the interchange between North and South America, a chronology of South American land mammal ages correlated with North American land mammal ages and European marine stages is proposed.

It is concluded that South America was an island continent through most of the Tertiary Period (ca 65 to about 3 Ma). As a result, the land mammal fauna of South America developed in isolation and was dominated by autochthonous endemic groups. Toward the end of the Tertiary (i.e., middle Miocene) a unique faunal balance had been achieved by the descendants of the ancient inhabitants (notoungulates, litopterns, condylarths, astrapotheres, edentates, marsupials) and of later (late Eocene) waif immigrants (caviomorph rodents, platyrrhine primates). A prominent feature of this mammal fauna was the combination of carnivorous and omnivorous marsupials with native placental herbivorous ungulates, subungulates, and edentates.

Sometime during the late Miocene, a limited but important interchange of mammalian taxa between North and South America took place. Procyonids (raccoons and their allies), a group of North American origin, first appear in South America in strata of Huayquerian Age, while members of the extinct South American ground sloth families Megalonychidae and Mylodontidae first appear in North America in early Hemphillian time. These groups dispersed along island arcs before the appearance of the Panamanian land bridge in the Pliocene (ca 3.0 Ma). Cricetine rodents, a group of North American origin, are first known in South America in strata of Montehermosan Age. The known taxa are too advanced and diversified to be considered the first of this group to invade South America. lt is believed by some workers that these rodents arrived before the Montehermosan, possibly in the late Miocene or earlier, by waif dispersal from North America.

The isolation of South America ended with the appearance of the Panamanian land bridge, which provided a direct, dry land connection between the two Americas. Across this portal an extensive interchange of terrestrial faunas occurred, and the fossil record documents an intermingling of these long-separated land mammals faunas.

      The beginning of this interchange by land route in South America is marked by the appearance of mammals which evolved from North American emigrants in the Chapadmalal Formation of Argentina. These include a mustelid (Conepatus), a tayassuid (Argyrohyus), and four genera (Akodon, Dankomys, Graomys, Reithrodon) of cricetine rodents. The appearance of this contingent of northern animals favors the existence of the Panamanian land bridge by this time. Likewise, a large number of terrestrial vertebrates of South American origin appear in North America in beds of late Blancan Age date around 2.7 Ma. Among the mammals are Neochoerus, Erethizon, Glyptotherium, Glossotherium, Kraglievichia, and Dasypus. 

The wear facets of primitive rodents can be homologized with those of primitive primates and ungulates. As in primates, the jaw movement was ectental, with an increased anterior component in the lingual phase (phase ll). The buccal phase (phase I) in rodents approaches the horizontal and it tends to be reduced in importance in comparison with the lingual phase. ln more advanced rodents the efficiency of grinding is increased by the development of additional cutting edges of enamel (e.g. enlargement of hypocone, development of mesoloph and lingual sinus). The buccal phase movement becomes lined up with the lingual phase movement to form a single oblique chewing stroke,resulting in planation of the crown. As the stroke becomes more longitudinal (propalinal) the enamel edges become more transverse. In Muridae propalinal chewing evolved before the loss of cusps, facets were reorientated and additional cusps developed.