Two new finds of pantodont materials from southern China, assigned to Archaeolambda, are described in this paper. One, a new species from the Nanxiong Basin, Guangdong Province, is similar to Alcidedorbignya inopinata from the early Paleocene of Tiupampa, Bolivia in size. It provides reliable evidence of the occurrence of Archaeolambda in the early-middle Paleocene of southern China. The second find includes specimens of Archaeolambda sp. cf. A. planicanina from the ?late Paleocene of Hengyang Basin, Hunan Province, which are the first record of a fossil mammal from the area near Hengyang city. The only vertebrate fossils previously found here were two genera of crocodiles discovered in 1938. This find sheds new light on the local biostratigraphy. 

Tarsals that can be confidently attributed to Paschatheríum dolloi from Dormaal (Belgium) are described. The astragalus is short; its broad neck is set at an angle of 30 degrees to the trochlea. The trochlea is pulley-shaped and proximally extended. There is no astragalar foramen. The medial tibial facet extends distally in a cup deeply excavated in the neck and buttressed. The sustentacular facet extends toward the navicular facet but is not fully confluent with it. The calcaneum bears a proximo-distally extended proximal facet for the astragalus. A relatively large peroneal tubercle projects from the body, and is situated distally. Functionally, the trochlea indicates extensive flexion-extension movements of the foot. Calcaneo-astragalar facets indicate sliding and rotation between the two tarsals. The inclination of the navicular facet suggests frequent foot inversion. The peroneal tubercle reflects good muscular capacities for foot rotation. Overall morphology is interpreted as a scansorial adaptation similar to that of sciurids.Comparisons are made with the tarsals of Macrocranion vandebroeki from Dormaal and Hyopsodus paulus from the Bridgerian of Wyoming. Some similarities between the astragali of Paschatherium and Macrocraníon (trochlea) are interpreted as convergences for rapid locomotion. However absence of mobility at the lower ankle and midtarsal joints in M. vandebroekzi suggests that this species was cursorial, as is known for M. tenerum from Messel. Similarities in the calcanea of Paschatherium and Hyopsodus are probably the result of close phylogenetic relations, and confirm the placement of Paschatherium in the hyopsodontids. The differences in the calcanea of Paschatherium and Macrocranion underline that Paschatherium is distinct from erinaceomorph insectivores. The differences in astragalar morphology between Paschatherium and Hyopsodus show that a marked adaptive divergence separates the two genera. We speculate about the common occurrence of a deep tibial cup (“cotylar fossa”) and a pulley-shaped trochlea in Paschatherium and hyracoids, suggesting that an adaptive scenario similar to that having led to Paschatherium (scansoriality) might explain the acquisition of the peculiar hyracoid tarsal characters; such a scenario contradicts the concept of Pantomesaxonia. Other peculiar characters of Hyopsodus suggest that hyopsodontids might be given more consideration in the search for hyracoid (and tethythere) origins. 

Evidence of 350 Lower Cretaceous Dinosaur footprints is pointed out in El Bayadh area. Their preliminary study allow to distinguish four trackway assemblages which reveal vertebrate bipedal presence forms of tri-and tetradactylous Dinosauroïds (Assemblages 1-3) and quadrupidal Sauropoïd (Assemblage 4).

The analysis of their footprint biometric features will attribute the quadrupidal Sauropoïd form to Brontopodus ichnogenus which is weIl known in the Jurassic and Cretaceous periods. In retum and despite their age, the dinosauroïd forms were approached, temporarily, to Grallator and Eubrontes types.

The occurrence of the dinosaur traces (Theropoïd and Sauropoïd) constitutes, in the Lower Cretaceous, an important first step of the knowlege of the marshy Reptilian fauna which takes over, from the begining of the Secondary Era, a wide paleogeographie area on the Southem Tethyan margin. 

Morphological and biometrical description of skulls, teeth, and limb bones of extant and fossil Old World herniones (including E. hydruntinus) and of New World 'stilt-Iegged' and other slender species from Blancan to Holocene. An Appendix presents ways in which the approximate size of some missing bones or dimensions may be deduced from available ones.

The discussed and/or illustrated fossils were found in Bolivia (Tarija), Canada (Yukon), China (Choukoutien, Gulongshan, Jiling, Loufangzi), Ecuador (Oil Fields), Ethiopia (Melka Kunturé), France (Lunel-Viel), Germany (Süssenborn), Greece (Agios Georgios, Petralona), Hungary (Dorog), Italy (Romanelli), Mexico (Cedazo, San Josecito), Mongolia (Sjara-osso-gol), Spain (Venta Micena), ex-Soviet Union (Akhalkalaki, Binagady, Chokurcha, Chukochya, Kabazi, Kolyma, Krestovka, Kurtak, Staroselie, Tologoj), USA (Alaska, Arkalon, Cedar Meadow, Channing, Conkling, Dry Mountains, Hay Springs, Leisey Shell Pit A, Lissie Formation, Natural Trap, Pool Branch, Powers Ranch, Rock Creek, San Diego, Santo Domingo, Seymour Formation, Shelter, Slaton, Trinity River). Numerous raw or statistically elaborated data are given in Tables.

There is no evidence for the existence of Old World hemiones in the New World nor of 'stilt-Iegged' equids in the Old World. The first 'stilt-Iegged' equid was found at Santo Domingo, New Mexico, and is believed to be Late Blancan. It was probably at the origin of E. calobatus (Arkalon, Rock Creek) and of the smaller E. semiplicatus (Channing, Rock Creek). Slender, but not 'stilt-Iegged', equids found at Natural Trap, Wyoming, ca. 12 ky ago belong to Amerhippus. AlI these species share with Oid World Sussemiones (and some hemiones) peculiar patterns on the lower cheek teeth.

The slender Equus sp. B of Leisey Pit A, Florida, ca. 1.2 Ma, as weIl as Amerhippus francisci and E. tau (probably a senior synonym of E. quinni) share conventional lower cheek teeth patterns. The skulls of A. francisci and E. tau, however, are quite different.

Paleontological data suggest a common origin of Amerhippus, Sussemiones, and 'stilt-Iegged' equids during the late Blancan. Old World hemiones seem to have differentiated later. 

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.

  

Abstract not available 

A new genus, Eppsillycteris, is erected for Adapisorex? allglicus COOPER, 1932, from the earliest Eocene Blackheath Beds of Abbey Wood, London, England. Various derived character states indicate that it belongs to the order Chiroptera (bats) rather than to the extinct "insectivore" family Adapisoricidae. Other derived character states are shared with fossil and modern members of the family Emballonuridae. Placement of the new genus in this family extends the record of the Emballonuridae back in time by about 10 million years. It is the earliest record of a modern bat family and one of the earliest bats. This implies that the differentiation of at least some modern bat families took place in the Palaeocene, where no authenticated records of bats yet exist. The primitive characters of the earliest bats make the family Nyctitheriidae an unlikely stem group for the order Chiroptera. A tentative plausible alternative exists in some unnamed upper molars from the Palaeocene of Walbeck, Germany. Wyollycteris chalix, described as a bat from the Late Palaeocene of Wyoming, U,S.A., fits better in the family Nyctitheriidae. 

The region of Porrentruy (Swiss Jura Mountains) is known for its rich and diverse assemblage of Late Jurassic coastal marine turtles (Thalassochelydia). Dominated by the “Plesiochelyidae”, this assemblage also includes representatives of the two other thalassochelydian groups, the “Thalassemydidae” and “Eurysternidae.” In this study, we present new shell-based material from Porrentruy referable to eurysternids. One specimen represents a juvenile individual or a relatively small taxon, and is notably characterized by a well fenestrated plastron exhibiting a wider than long central plastral fontanelle. Two other specimens are much larger and possibly represent the largest eurysternids known to date. The fourth specimen is characterized by a unique plastral morphology otherwise only known in very small juveniles. This is the first time this unique plastral morphology is known to persist in an adult or subadult. The new material described herein represents at least three distinct taxa, all of them probably new. However, we refrain from naming new species based on this incomplete material in order to avoid adding confusion to an already complex taxonomical situation. This study provides new insights into the great diversity of eurysternids during the Late Jurassic. 

In this article is described a new species of Nyctitheriidae with primitive characters: Leptacodon nascimentoi n. sp. from the early Eocene of Silveirinha (Portugal). 

The stapes is the last of the middle ear ossicle chain and the smallest bone of the mammalian skeleton. Because it rests on the membrane of the fenestra vestibuli during life, the stapes may often fall within the bony labyrinth cavity when soft structures decay after death. In this work, we highlight the unexpected role that the bony labyrinth plays in the preservation of the stapes. Systematic investigation of the bony labyrinth of 50 petrosal bones of extinct and extant artiodactyls led to the discovery of eight cases of “intralabyrinthine” stapes. Three dimensional reconstructions of these stapes allow documenting stapes morphology of four extinct artiodactyl taxa: Microstonyx erymanthius (Suidae), Elomeryx borbonicus (Hippopotamoidea), ?Helohyus plicodon (Helohyidae), and an undetermined Cainotheriidae; and four extant ones Choeropsis and Hippopotamus (Hippopotamidae), and Tayassu and Phacochoerus (Suoidea). ?Helohyus plicodon from the Middle Eocene documents the oldest stapes known for the order Artiodactyla. Morphological study and metric analyses of our sample of artiodactylan stapes show that stapes are likely to carry relevant phylogenetic characters/signal within artiodactyls, and a potential Euungulata signature. 

The investigations undertaken at Crivadia (Hateg Depression, Hunedoara District, Romania), the type locality of Crivadiatherium mackennai RADULESCO el al. (Radulesco, Iliesco et lliesco, 1976), led to the discovery of remains of a new Embrithopod. Close to the above mentioned species, but larger in size, this animal is here described as a new species of Crivadiatherium, C. iliescui. ln addition, the comparison made between the forms indicated above and Palaeaamasía kansui OZANSOY from the Eocene deposits of Anatolia (Ozansoy, 1966; Sen et Heintz, 1979) showed that the latter species included a heterogeneous material; this permitted us to distinguish the form in the Anatolian locality Ciçekdag-Arabin Kôyü under the name Palaeoamasia sp. The geographical distribution and diversity of the Embrithopod species under discussion (Balkan, Anatolia) support the idea of an eurasiatic origin of this group and seem to suggest the existence during the Eocene of a particular faunal province in south-eastern Europe. 

Anthracotheres from the Pondaung Formation, Myanmar, are considered as one of the most primitive artiodactyl groups and they represent the oldest known record in the world. Thus, the understanding of this group has numerous implications for evolutionary biology and biochronological correlations. However, the systematlcs of these mammals has been interpreted in different ways, and the main debate focuses on the number of taxa represented in the Pondaung Formation. The revised taxonomy proposed here is mainly based on the relative development of the upper molar W-shaped ectoloph, system of crests and stylar cusps, and on body size. On the basis of these characters, they are classified into four genera including six different species. Two well-known genera, Anthracotherium and Anthracokeryx, are validated and more precisely diagnosed. Anthracokeryx possesses a better developed W-shaped ectoloph, system of crests and stylar cusps than Anthracotherium, which displays notable differences with the more derived representatives of this genus. Both of these Pondaung genera show evidence for sexual dimorphism. However, the incompleteness of fossil material fueled a debate concerning the status of two additional Pondaung anthracotheres, Siamotherium and Anthracohyus. The latter genus is of uncertain affinities, but it has been considered as a hippopotamid ancestor. Despite new material attributed to these two forms, additional discoveries are still required to establish their taxonomic status. The hypothesis that Southeast Asia was the centre of origin of Anthracotheriidae is supported by the retention of numerous primitive dental characters in these taxa and by the antiquity of the Pondaung Formation, to which an age of 37 My is now generally accepted. 

Re-evaluation of the small collection of mammal fossils from the Changxindian Formation near Beijing, China indicates the following taxa are present: Eutheria, Hypsimilus beifingensis, cf. Miacis sp., Anthracotheriidae and Forstercooperia grandis. The presence of Forstercooperia grandis indicates an Irdinmanhan age and does not support previous assignment of a Sharamurunian age to the Changxindian Formation. 

Tetraceratops insignis is known from a single, crushed skull from the Lower Permian of Texas. Its unique proportions and osteological details gained central meaning in the question of the origins of Therapsida since this early synapsid has been determined as the oldest and less derived therapsid. Apart from Tetraceratops, the ‘mammal-like’ Therapsida and their sister, the pelycosaur-grade Sphenacodontidae, are separated by one of the longest ghost lineages in tetrapod fossil record. However, the minor, though well justified critique faced insistent publication regarding the therapsid hypothesis. A carefull re-evaluation of the holotypic skull reveals that therapsid traits cannot be supported, including a rejection of the formerly supposed adductor shelf in the temporal fenestra. Increased understanding of ‘pelycosaur’ character variation underlines a haptodontine-grade or, less likely, sphenacodontid position for Tetraceratops. 

The discovery in the Turolian (Late Miocene) of Dytiko 3 (Macedonia, Greece) of a complete skull with mandibles and cervical vertebrae, atlas and epistropheus, is a very important contribution to the knowledge of the subfarnily Chalicotheríinae. After the description, the comparison with other specimens of Miocene chalicotheres permits the revival of the generic name Macrotherium with a new species M. macedonicum. This genus is mainly characterized by a short snout and an inflated cerebral skull. It coexists during the Miocene with Chalicotherium. A cladistic analysis leads to conclusion that the species which has been described from the Early Middle Miocene of Rusinga must be identified as the type-species of a new genus: Butleria.





  

Systematische Zoologie by A. REMANE, V. STORCH, and U. WELSCH.
1986, Edition 3. Cloth and paperbound. Stuttgart and New York : Gustav Fischer Verlag.
xvi + 698 pp. DM 86. (Geb.) & DM 72 (kart.). 

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. 

Abstract not available 

Biographie et liste des publications de S. Garimond. 

Since the 19th century, thousands of footprints were observed in the geological series of the French Mesozoic. All are located in the Triassic and Jurassic. After a promising beginning, in France, it is only a few papers which will be published in the first half 20th century, unlike the USA and of others countries of Western Europe. One ought to wait about 1950 for a revival and now they are nearly 200 papers which were devoted to the ichnofossils. The literature abundance and the renewed interest of the naturalists for the palichnologic studies decided to us to write a synthesis work. This one begins with a stratigraphic inventory in which, localisation, age and paleontological contents of about 180 fossiliferous sites are specified. After having pointed out the followed methods, the footprints paleontological interpretation is then approached in detail and the results obtained are replaced in stratigraphy to deduce the fauna evolution during the Mesozoic. So, it appears that Ichnologic data, more varied and rich in the Triassic and Liassic than those relating to the bones, very rare for the considered periods, are very informative. The middle Triassic (Anisian-Ladinian), thus reveals Cotylosauria, Lepidosauria, Crurotarsi with Rauisuchia, Ornithosuchidae, Crocodylia and Dinosauromorpha more the "Prodinosauria": Dinosamiforme whose skeletons are known in Argentina but only in Ladinian. The rather fast domination of Dinosaurs during Norian is also as well shown. The almost exclusive presence of their footprints, up to fifty cm long, in the Lower Hettangian indicates their supremacy in the environments. Footprints characterise not very deep life places located between inter-supratidal limits and often out of water. Sedimentologic and Palaeontologic studies showed that they were great coastal spaces during Middle Triassic, flood-plain with sebkhas while Upper Triassic, and a large !!coastal marsh!! in Grands-Causses during Liassic in which, mainly, fine stromatolithic layers were deposited. During the same periad, bay beaches spread in Vendée. During the Middle Jurassic, they are also brackish to lacustrine environments and recifallagoons in- the Upper Jurassic. Numerous measurements of the footprints and trackways directions showed that the animaIs moved there in weil defined directions, for long periods. They seem due to the palaeotopography of the life environments relatively stable. Also, the discovery of vegetal radicular networks and small footprints far away from the continental borderlands has suggested that the animals continuously lived in these palaeoenvironnements, belonging to large ecosystems, where the sedimentation rate was weak. This explains that thebadies could not fossilize there but only their footprints through the cyanobacterian action in main cases. From the vertical distribution of different ichnospecies, defined with adapted statistical methods, explained in this work, a palichnostratigraphy was established for the Middle Triassic. Although the footprints are also abundant in Hettango-Sinemurian of "Grands-Causses" and the Vendée, it was not possible, up to now, to establish any zonation in this series; Probably because the palichnofauna is too little diversified there, currently reduced to a majority of Theropods II-IV tridactyl traces.