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). 

Simpson (1937a) reconstructed the brain of the Paleocene multituberculate Ptilodus as having the olfactory bulbs widest anteriorly, an unusual condition among mammals. Slight preparation and reexamination of the endocast specimens of Ptilodus reveals that the olfactory bulbs in fact taper anteriorly, as in the recently-described endocranial casts of three multituberculate species from the Late Cretaceous of Asia, and as in those of other mammals. The brain of Ptilodus was therefore essentially of the same general pattem as in other multituberculates. Ptilodus differs, however, in having the vermis more deeply inserted between the cerebral hemispheres. Other details concerning the endocast morphology of Ptilodus are clarified.

The encephalization quotient (EQ) of Ptilodus is recalculated from revised estimates of both endocranial volume and body mass to fall somewhere within a broad range of values; from 0.41 to 0.62 if the olfactory bulbs are included and from 0.37 to 0.55 if they are not. In any case, the relative brain size of Ptilodus is roughly equivalent to that of Chulsanbaatar, the only other multituberculate for which EQ has been calculated, but considerably smaller than that of an average extant mammnal. 

Le groupe des Mustélides « Ischyrictoïdes » développe des tendances évolutives qu’engendrent des formes de Carnassiers prédateurs robustes et de grande taille. C’est une évolution comparable à celle que l’on trouve chez Plesiogulo, qui, lui, a une origine énigmatique (Petter, 1963). Chez les Mustélides on peut signaler deux lignées assez nettes : celle du sous-genre nominal des Laphyctis, plus conservatrice, plus mustéliforme, renfermant les espèces Ischyrictis (Laphyctis) mustelinus VIRET et L. zibethoides BLAINVILLE ; celle de type félinoïde caractérisée par L. Ginsburg (1961) avec la forme type Ischyrictis (Hoplicitis) florancei du Vindobonien inférieur de Pontlevoy-Thenay et I. helbingi VIRET, 1951 du Vindobonien supérieur de la Grive Saint-Alban. De plus rappelons que I. vorax DEHM et I. comitans DEHM du Burdigalien de Wintershof-West sont sans rapport avec les espèces du Miocène supérieur (Ginsburg, o.c.).

Récemment G. Petter (o.c.) a montré la difficulté qu’il y avait à envisager que l’Ischyrictis de Can Llobateres qu’elle décrivait puisse être le descendant de Ischyrictis helbingi de La Grive : la forme plus récente est évidemment de plus grande taille, mais le développement très marqué et la position avancée du protocône paraissent constituer un obstacle à une telle filiation.

Donc on signalait jusqu’ici deux lignées de Mustélides « ischyrictoïdes » toutes deux de grande taille : d’une part I. zibethoides de Sansan, d’autre part I. helbingi de la Grive. Or à notre point de vue nous considérons actuellement qu’il existe très probablement trois phyla d’Ischyrictis. Le premier serait représenté par les formes burdigaliennes déjà nommées I. vorax et I. comitans ; il se caractériserait par la perte précoce de la P₁ inférieure et la forme spéciale de la canine inférieure. Ce premier ensemble pourrait être rassemblé dans le sous-genre Laphyctis. Le reste des ischyrictoïdes de type conservateur, pour ce qui est de la région des prémolaires et de la forme de la canine, pourrait être subdivisé en deux sous-genres : le sous-genre Ischyrictis désignant les formes les plus mustéliformes avec I. mustelinus et I. zibethoides d’une part, et le sous-genre Hoplicitis pour les formes félinoïdes avec I. florancei et I. helbingi. 

L’Encyclopedia of Paleoherpetology, Part 17A : Pelycosauria de Robert R. Reisz (1986) offre une synthèse complète des synapsides les plus primitifs et les plus anciens, essentiels pour comprendre l’évolution précoce de ce groupe majeur de vertébrés. L’ouvrage commence par un historique, suivi d’une analyse ostéologique détaillée du crâne, du squelette axial et appendiculaire. 

Pangolins have never shown a high taxic diversity and their fossil record is scarce. We report here the first discovery of a partial humerus from late Oligocene deposits in Pech du Fraysse (MP28, France). The new specimen from Pech du Fraysse is described and compared to various extant and extinct species of pangolins. It shows a suite of morphological features very similar to the humeri discovered in Saint-André (MP 26), Solnhofen (Burdigalien), and Saulcet (Aquitanian), attributed here to Necromanis franconica. The description of the specimen from Pech du Fraysse allowed us to discuss the systematics of Paleogene and Neogene pholidotans. The differences between PFY 4051 and N. franconica on the one side, and N. quercyi on the other side, might be sufficiently important to justify a generic distinction. A comparison with extant species showed that N. franconica was likely terrestrial and fossorial based on its humeral morphology. 

When the first edition of Mike Benton’s Vertebrate Palaeontology came out in 1990, sauropods still dragged their tails on the ground, the closest relatives of whales were mesonychids, and Mesozoic birds consisted essentially of Archaeopteryx, Ichthyornis and Hesperornis. Twenty-five years later, the book, now in its fourth edition, is a third longer, in a larger format and sports fine colour plates – in addition to a companion website. 

Micro-CT imaging is an increasingly popular method in paleontology giving access to internal structures with a high resolution and without destroying precious specimens. However, its potential for the study of hypoplasia defects has only recently been investigated. Here, we propose a preliminary study to test whether hypoplastic defects can be detected with micro-CT (μCT) scan and we assess the costs and benefits of using this method instead of naked eye. To do so, we studied 13 fossil rhinocerotid teeth bearing hypoplasia from Béon 1 (late early Miocene, Southwestern France) as positive control and 11 teeth of the amynodontid Cadurcotherium (Oligocene, Phosphorites du Quercy, Southwestern France), for which enamel was partly or totally obscured by cement. We showed that all macroscopically-spotted defects were retrieved on 3D reconstructions and selected virtual slices. We also detected additional defects using μCT scan compared to naked eye identification. The number of defects detected using μCT was greater in the Cadurcotherium dataset (paired-sample Wilcoxon test, p-value = 0.02724) but not for our control sample (paired-sample Wilcoxon test, p-value = 0.1171). Moreover, it allowed for measuring width and depth of the defects on virtual slices (sometimes linked to stress duration and severity, respectively), which we could not do macroscopically. As μCT imaging is both expensive and time consuming while not drastically improving the results, we recommend a moderate and thoughtful use of this method for hypoplasia investigations, restricted for instance to teeth for which enamel surface is obscured (presence of cement, uncomplete preparation, or unerupted germs). 

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.