The composition of assemblages of lizards and Amphisbaenian from the European Eocene are described. At least ten lizard families are identified from the lower European Eocene levels. Eight are still recorded in the last level (Escamps) of the late Eocene. Agamid lizards (genus Tinosaurus) died out by the end of the lower Eocene and Varanid lizards (genus Saniwa) disappeared by the beginning of the late Eocene. Amphisbaenians are recorded throughout the Eocene in Europe. The lacertilian fossil record of Europe and North America show a high degree of faunal resemblance in the early Eocene, followed by a decrease during the later part of the epoch. The lacertilian and amphisbaenian faunas from the European Eocene are not subject to great variations during the period; this is in contrast with the mammal record at the same time. It is argued that the low metabolic rates and the ectothermy of lizards could explain those differences, along with the increasing insularity of the West European area during the late Eocene time.

  

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. 

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 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.

  

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.

  

L'ouvrage est divisé en trois grandes parties traitant successivement: I. l'anatomie ("Proboscidean flesh and bones"), en abordant la taxonomie, l'allure générale et l'éco-éthologie des proboscidiens actuels et fossiles; II. les causes de mortalité collective naturelle et provoquée chez les actuels; III. les documents fossiles et l'extinction des formes anciennes d'Amérique du Nord. 

Avec ce volume se clôture l'étude géologique et paléontologique des sites à hominidés de Koobi Fora. Il fait suite aux deux précédents ouvrages, parus respectivement en 1978 et 1983, consacrés également à l'étude des faunes recueillies sur ces gisements dans le cadre du Koobi Fora Research Project. 

Functional morphology invertebrate paleontology, édité par Jeffrey J. THOMASON, 1995. Cambridge University Press, xi + 277 p. ISBN 0-521-44095-5, f. 45,00 ($ 69,95).

La morphologie fonctionnelle appliquée aux fossiles demeure un sujet à la fois passionnant et important. Passionnant, car elle s'adresse à des êtres disparus, aux combinaisons de caractères parfois inattendues et sans contrepartie chez les formes actuelles. Sujet important, car il faut, au delà de la constatation classique de l'adéquation de la forme des organes à leur fonction, expliquer l'origine des structures par évolution. L'évolution ou descendance avec modification, implique que les êtres vivants sont reliés les uns aux autres et qu'i! est possible de tenter à l'aide d'un raisonnement par inférence, la caractérisation des ancêtres en fonction des traits des formes auxquelles ils ont donné naissance. Mais il faut ajouter que par sa fonction, la structure relie immédiatement l'animal à son milieu puisqu'elle assure un rôle biologique. 

L’article analyse les poches à phosphorite d’Aubrelong (Quercy), comparant les fouilles de 1937 (Éocène supérieur) et celles des années 1967-1970 (Oligocène inférieur), révélant une stratification contrastée : argiles brunes pauvres en fossiles en surface, et argiles rouges riches en phosphates et faune en profondeur. Les analyses géochimiques confirment une origine latéritique sous climat tropical humide, avec des remplissages tantôt stratifiés, tantôt chaotiques, remettant en cause l’hypothèse d’une progression chronologique uniforme des dépôts 

Cet article présente les premières données sur les Carnivores fissipèdes des Phosphorites du Quercy, issues de fouilles récentes (1971-1972). Les fossiles se répartissent de l'Oligocène inférieur à supérieur. 

The entelodonts of the Quercy phosphorites are essentially known from isolated teeth. The skull remains attributed to Entelodon magnum by Kowalewsky in 1876 and the type left mandible of Enteladon depereti RÉPELIN, 1918 do not belong to this family. From a morphologic point of view, the teeth from Quercy are quite comparable to those from the type localities of E. magnum and E. deguilhemi. In the absence of distinctive anatomical criteria between E. magnum (small species from the level of Ronzon) and E. deguilhemi (large species from the level of Villebramar) they are referred, according to their size, to one or the other of these two species. However, some of them are intermediate in size. Their existence speaks in favor of a close relationship between E. magnum and E. deguilhemi and confers a real stratigraphic interest to these entelodonts of Western Europe. Finally, some anatomical characters (notch on the mesial border of P4, presence of a paraconid joined to the metaconid, trigonid higher than talonid) considered until now as peculiar to the North American Archaeotherium and not yet cited in its European contemporary Entelodon have been brought to light on the teeth from Quercy.

  

La faune de Rongeurs d'Escamps (Lot) bien que relativement pauvre en espèces (dix) s'avère riche d'enseignement pour les Rongeurs de l'Oligocène inférieur d'Europe Occidentale. Cette periode semble caracterisée par une cladogenèse des Théridomyines. A Escamps, un nouveau genre (Patriotheridomys) est décrit ainsi qu'une nouvelle espèce de Theridomys. Avec Oltmamys platyceps, décrit ici plus complètement et désormais bien situé stratigraphiquement, les deux espèces précédentes constituent un ensemble original du Sud de la France. A la même époque, en Angleterre, Allemagne et Espagne, des espèces «régionales» de Théridomyinés se dersifient.  A côté de ces formes qui ne semblent pas franchir la «Grande Coupure» sont représentées deux lignées d'Issiodoromyinés (Elfomys sp et Pseudoltmomys cuvieri), une de Théridomyiné (T. (Blainvillimys) rotundidens) ainsi qu'un Gliridé, Gliravus priscus (que l'on différencie nettement de la deuxième lignée des Gliravus oligocènes : G.  meridionalis -> G. majori). On retrouve ces formes dans les gisements plus récents du niveau de Hoogbutsel où elles sont à peine plus évoluées. Le fait que les degrés évolutifs de ces lignées soient très proches laisse supposer que le laps de temps séparant les niveaux d'Ecamps et Hoogbutsel fut relativement court. 

Cet article présente une étude détaillée du genre Stehlinia, un chiroptère du Paléogène d'Europe, basé sur un matériel abondant issu notamment du gisement d'Escamps (Quercy). L'analyse révèle que Stehlinia possède un mélange de caractères primitifs (comme une denture tribosphénique complète et des prémaxillaires soudés) et évolués (notamment dans le squelette post-crânien), le rapprochant des vespertilionoïdes actuels, en particulier des Kerivoula. 

The genus Pachynolophus, one of the poorest known of the Palaeotheriidae, includes the brachyodont forms with reduced and non-molariform premolars and with upper molars lacking a mesostyle. Quantitative characters (divers surface indications and elongation of the teeth), while demonstrating a close relationship to Hyracotherium, permit a better differentiation of the genus, confirm its specific splitting, and permit the distinction of three lineages. The skull from Memerlein is taken as the type of a new species, P. Iavocati, of which the dentition is extremely characterized by its lophiodonty, the strong reduction of the premolars and the reduction of the cingula. This characterization testifies to a late age which extends the existence of the genus quite near to the Eocene-Oligocene limit. Compared with the only two skulls known of related species (Hyracotheríum vulpiceps and Pachynolophus Iivinierensis), that from Memerlein is distinguished by progressive characters affecting diferent regions but most particularly the braincase; it is not possible, however, to isolate within this evolution the part which leads to a systematic differentiation. Modernization is translated by a considerable increase in size of the braincase, principally in the frontal region, a development of the facial region with anterior displacement of the dental series and a greater specialization of the masticatory apparatus. This evolution parallels the history of the Equidae of the North American early Tertiary, but certain particularities, the form of the alisphenoid, the presence of an anterior frontal foramen, and the structure of the paroccipital apophysis, testifies to the independance of the European forms. 

The Palaeobatrachidae until now have not been reported from France. The present note makes known the discovery of very significant remains in three Tertiary localities of France: Cernay (late Paleocene), Laugnac (late Aquitanian) and Sansan (middle Helvetian). The osteologic characters, as well as the geographic and stratigraphic distribution of the family are re-stated with added details. The Palaeobatrachidae are a European family known from the late Jurassic of Catalonia (publication in course by J. Seiffert) to the Plio-Pleistocene (pre-Mindel) of Poland and Rumania. By their way of life and certain osteologic characters they are similar to the Pipidae, but they are distinguished by profound differences. It would be rash to include them in the Pipoidea or even in the Aglossa. They are apparently an independant group, essentially holarctic, which held in Europe a role equivalent to that played by the Pipidae south of Tethys. 

The present work is devoted to the study of the Cretaceous and Tertiary fishes (teeth of Selachians, Actinopterygians and Dipnoans) collected during a recent expedition in Niger. The Maestrichtian localities have yielded a new genus and a new subspecies of Selachian: Igdabatis sigmodon nov. gen., nov. sp. and Lamna biauriculata nigeriana nov. subsp. The locality of Sessao, which has been attributed to the Thanetian by means of the study of the fish, has furnished by screen-washing an interesting fauna wherein six new species are described: Raja Iouisi, Dasyatis sessaoensis, D. sudrei, D. russelli, Hypolophites thaleri and Ceratodus casieri. Comparison of these faunas with contemporary faunas of Africa has brought out a certain endemism in the Iullemmeden Basin during the late Cretaceous and the early Tertiary. 

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. 

A critical review on the literature about the parataxonomy of amniote eggshells reasserts the great interest of this systematics tool for the progress of dinosaur eggshell paleontology. However, shedding light on its limits, we propose to give up the use of the basic types - morphotypes key system. 

Paleosols and the taphonomy of vertebrate fossils in the Eocene Kuldana Formation of northern Pakistan provide important information on the preservation and time-averaging of fossil assemblages. Morphologic, mineralogic, and chemical data as well as comparisons with Quaternary soils suggest that Kuldana paleosols formed under generally dry and oxidizing conditions over time intervals of less than 100 000 years and perhaps as short as 1000 years. The distribution of carbonate in Kuldana paleosols further indicates that the upper half of the profiles were acidic whereas the lower halves were alkaline. Vertebrate fossils are rare in Kuldana paleosols and occur primarily in well-cemented sandstones and conglomerates with abundant micritic and iron-stained nodules that were reworked from floodplain soils. The scarcity of vertebrate remains in Kuldana paleosols probably reflects a combination of acidic, dry, and oxidizing conditions in the upper half of the profiles and rapid floodplain sedimentation. Comparisons between the taphonomic characteristics of Kuldana channel fossil assemblages and bone accumulations in modem rivers provide a basis for estimating the length of time represented by Kuldana fossils from several important localities. Vertebrate fossil assemblages from Barbora Banda are characterized by a low-diversity paleofauna, partially articulated skeletons, and bones that are sorted by size and shape. Comparison with bone accumulations in modern rivers suggests that the fossils from Barbora Banda accumulated in 1 to 10 years. Vertebrate fossils from the Lower Kuldana in the Kala Chitta Hills region, typified by locality H-GSP 62, are characterized by a high-diversity paleofauna and generally random and unsorted fossil bone distributions, which suggest that the fossils from these localities represent longer time intervals than the Barbora Banda fossils. Based on the time estimates for Kuldana paleosol development, fossil assemblages in Kuldana channel deposits in the Kala Chitta Hills region probably represent time intervals of about 1000 years. 

A partial skull of Ardynomys russelli sp. nov. (Rodentia, Cylindrodontidae) is described. This was collected in the late Eocene of Alag Tsab locality in the eastem Gobi Desert, Mongolia. Ardynomys russelli sp. nov. is characterized by small size, brachyodont molars, and retention of P3. It represents the earliest record of the genus Ardynomys MATTHEW & GRANGER, 1925, in Asia.