A new example of parallelism in the dental pattern ofthe Theridomyidae is illustrated by the description ofa new species: Theridomys Iudensis from the standard level of Antoingt (middle Oligocene). Considering the occurence ofthis parallelism phenomenon. the use of numerous qualitative and quantitative criteria is essential to characterize the different stages ofthe different evolutive lineages. Thus, a new simple parameter is proposed (CHY = H+l/0,5 L) to estimate hypsodonty of the medium hypsodont Rodentia. 

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. 

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.

  

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 object of this work is the study of the artiodactyls of the karstic locality of Lissieu near Lyon. Among the sixteen species counted, five (Hyperdichobune nobilis, Hyperdichobune sp., Haplabunodon mulleri, Tapirulus depereti and Pseudamphimeryx schlosseri) are cited for the first time in this fauna. The description of part of the anterior dentition of «Dichobune» langi permits the referal of this species to the genus Hyperdichobune. The new selenodont species Dichodon lugdunensis  described in this work belongs, with its ancestor Dichodon simplex, to a lineage distinct from that of Dichodan cartieri and Dichodon ruetimeyeri. Finally, the taxonomic reality of the Lissieu species, Lophiobunodon rhodanicum Deperet, is justified. All the other species have been compared with those of Egerkingen. Even though with most of them no difference in age can be shown between the two deposits, some however indicate clearly by their degree of evolution that Lissieu is slightly more recent than Egerkingen. ln the history of Eocene mammals, the Lissieu fauna, because of its homogeneity, can be considered as a sure reference fauna of the Auversian period. 

The reproductive biology of living birds differs dramatically from that of other extant vertebrates. Distinctive features common to most birds include a single ovary and oviduct, production of one egg at daily or greater intervals, incubation by brooding and extensive parental care. The prevalence of male parental care is most exceptional among living amniotes. A variety of hypotheses exist to explain the origin of avian reproduction. Central to these models are proposed transitions from a condition of no care to maternal, paternal or biparental care systems. These evolutionary models incorporate a number of features potentially preservable or inferable from the fossil record (integument, skeletal adaptations for flight, egg and clutch size, nest form, hatchling developmental stage, the number and function of oviducts, and the mode of egg incubation). Increasing availability of data on dinosaur reproduction provides a means of assessing these hypotheses with fossil evidence. We compare dinosaur data to a selection of models that emphasize maternal, paternal or biparental care. Despite some congruence with dinosaur features, no single model on the evolution of avian reproduction conforms fully to the fossil record, and the ancestral parental care system of birds remains ambiguous. Further investigation into dinosaur parental care, nest structures, clutch geometry, egg-pairing, eggshell porosity, and embryo identification may eventually resolve these issues.  

A new Tertiary megadermatid is described from Rackham's Roost Site, a Pliocene limestone cave deposit on Riversleigh Station, northwestern Queensland, Australia. It appears to represent the first Australian record of Megaderma GEOFFROY, 1810, a genus otherwise known from Tertiary African and European taxa and the living Asian species M. spasma (LINNAEUS, 1758) and M. (Lyroderma) lyra PETERS, 1872. Megademza richardsi n. sp. is one of the smallest megademiatids known. It exhibits a mixture of plesiomorphic and autapomorphic features, the latter appearing to exclude it from being ancestral to any living megadermatid. The new species is one of eight megadermatids identified from the Australian fossil record, most of which are referable to Macroderma MILLER, 1906. 

This paper is about the oldest African rodents faunas, from the late Early Eocene, or early Middle Eocene, Glib Zegdou (Algeria) and Chambi (Tunisia) localities. Five species are described and figured, belonging to a new family here created, the Zegdoumyidae.

This family is compared to the Early and Middle Eocene rodents families from Asia, Europe and North America (Chapattimyidae, Yuomyidae, Gliridae, Theridomyidae, lschyromyidae and Sciuravidae), as well as to those known from the Late Eocene African locality Bir El Ater (Anomaluridae and Phiomyidae).

On the one hand, it seems clear that the African endemic Anomaluridae arise from the Zegdoumyidae. On the other hand, the lschyromyidae, or primitive Sciuravidae, may be the most reliable ancestral groups for the Zegdoumyidae. Thus, this new family can be considered as the sister group for the American Sciuravidae on the one hand, and for the European Gliridae on the other hand.

The biogeographical consequences of these phylogenetic hypotheses are discussed. A new phase of communication between Europe and North Africa is inferred, during the Early Eocene. It has been followed by a short period of endemism, allowing the adaptive radiation for the Zegdoumyidae, preceding the immigration of the Phiomyidae, during the Late Eocene, probably from Asian relatives. 

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. 

The ventral face of the Paulchoffatiinae skull (Multituberculata, Lower Kimmeridgian, Portugal) is new reconstructed. Some details hitherto unknown are added, as the presence of jugals, the structure of the palatine and the extension of the pterygoids. The situation of the m2/ is discussed. Kielanodon hopsoni n. g., n. sp. is erected, known by its upper p3-5/. From Guimarotodon leiriensis the mandible with its dentition is made known. New informations concerning the milk-dentition and the replacement of teeth are also added. 

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. 

Based on material from 30 localities, morphologic dental, cranial and biometric analyses have permitted the characterization of two parallel Issiodoromyine lineages, and also the definition of diverse species representing several evolutive stages. Thus it is that new lineages complete the contribution made by the Theridomyinae and Cricetidae and permit, for the Quercy in particular, additional precision in the biochronologic succession of the localities. One of the lineages is limited to the genus Pseudoltinomys LAVOCAT; the other evolves from the genus Elfomys HARTENBERGER to the genus Issiodoromys BRAVARD in GERVAIS. The latter is affected by profound anatomical changes due to a functional modification of the mastication apparatus. These changes seem to be able to be put in relation with the aridification and cooling of the climate at the end of the Eocene. At the end of the middle Oligocene, a new chewing structure is achieved. It is found in diverse living rodents that inhabit a rather arid steppe environment (Cavia, Pedetes, Ctenodactylus). To these supposed nearby ecologic conditions, these rodents have responded in a convergent fashion. It is possible to attribute to the extreme specialization of Issiodoromys its incapacity to adapt to the new climatic crisis of the end of the Oligocene. The arrival of immigrants may be considered as another cause of its disappearance at this time, complementary or not with the first. 

The small insectivorous placental mammals from Ste-Néboule are poorly varied. Two orders of insectivores are documented : the Proteutheria by Pseudorhyncocyon cayluxi (leptictids), the Lipotyphla by Saturninia gracilis and S. beata (nyctitheriids). The bats are only rhinolophoids and mostly hipposiderids. Sufficient populations allow us to restrict the original definitions of three previous species (Hipposideros schlosseri, Palaeophyllophora quercyi, P. oltina). From now, these species can be regarded as monophyletíc. 

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 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. 

Perutherium altiplanerise THALER, 1967 from the Late Cretaceous of Peru has long been recognized as South America's oldest known placental mammal. Since its description Perutherium has been generally regarded as having condylarth affinity Based on our identification  of a unique notoungulate synapomorphy we recognize Perutherium as the oldest and the most generalized known member of that order. This new determination and the large taxonomic diversity (five families) of notoungulates in rocks of Paleocene age in Argentina and Brazil, favor a South American origin for this group. The occurrence of notoungulates in rocks of Late Paleocene age in Asia and North America is explained by dispersal of a notoungulate stock from South America to North America and from there to Asia. 

Valverde's cenogram method is used to analyse mammalian communities from the late Eocene to late Oligocene of southern France, mainly from the "Phosphorites du Quercy". Cenogram analysis involves plotting the size of each component species in a fauna on a semilog diagram in rank order, permitting fossil faunas to be compared with Recent ones. The configurations of Recent communities serve as models for establishing the general environmental characteristics of fossil mammalian faunas. This method of analysis applied to faunal sequence can reveal major and sudden ecological perturbations. The paleobiogeographical event (i.e. the mammalian immigration wave) at the Eocene-Oligocene Boundary in western Europe, known as the «Grande Coupure", is here shown to represent a drastic and sudden ecological change: late Eocene tropical environments in Europe deteriorated rapidly turning to subdesert or desert environments al the beginning of the Oligoccne. 

Equus caballus antunesi, nova subspecies, was a hypsodont, slender, and rather small horse (around 141cm at the withers), with narrow hooves and protocones longer on P3/-P4/ than on M1/-M2/. It does not fit in any of the different "types" of Pleistocene caballine horses previously recognized but may be related to the horse from the Acheulean of Solana del Zamborino.
Hypsodonty, small size, slenderness, narrow hooves are all characters that can easily be related to ecological conditions. Equus caballus antunesi was probably a horse adapted to rather dry and cold conditions and to a hard ground. It does not seem related at all to the North-European Equus caballus germanicus-gallicus group. 

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 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.