Clavicles and interclavicles are plesiomorphically present in Reptilia. However, several groups show reduction or even loss of these elements. Crocodylimorpha, e.g., lost the clavicles, whereas dinosaurs are generally interpreted to only preserve the clavicles, the theropod furcula representing an unique case of fused clavicles. In sauropods, reports of clavicles are relatively frequent in non-titanosauriforms. These elements are elongated, curved, and rather stout bones with a spatulate and a bifurcate end. However, they were always found as single bones, and differ from the relatively short and unbifurcated clavicles found articulated with the scapulae of basal sauropodomorphs. Elements from the Howe Quarry (Late Jurassic; Wyoming, USA) shed new light on these interpretations. Besides the elongated, curved bones (herein named morphotype A), also pairs of symmetric, L-shaped bones were recovered (morphotype B), associated with diplodocid dorsal and cervical vertebrae. Elements resembling morphotype B - articulated between the scapulae - have recently been reported from a diplodocid found near Tensleep, Wyoming. Taphonomic evidence, as well as the fact that they were preserved in symmetrical pairs, therefore implies that morphotype B represents the true sauropod clavicles. Contrary to earlier reports, morphotype A elements from the Howe Quarry, as well as of previously reported specimens show a symmetry plane following the long axis of the elements. It is thus possible that the morphotype A elements were single bones from the body midline. The only such element present in the pectoral girdle of tetrapods are the interclavicle and the furcula. Comparison with crocodilian and lacertiform interclavicles indicates that the bifurcate end of the sauropod elements might represent the reduced transverse processes of the anterior end, and the spatulate end would have covered the coracoids or sternal plates ventrally. The presence of both clavicles and interclavicles in the pectoral girdle stiffens the anterior trunk, and enhances considerably its stability. Such an enforcement might have been needed in diplodocids due to the strong lateral forces induced to the fore-limbs by the posteriorly placed center of mass (due to shorter fore- than hind-limbs), as well as lateral movements of the enormously elongated necks and tails. The absence of clavicles and interclavicles in titanosauriforms coincides with the development of wide-gauge locomotion style. The presence of interclavicles in sauropods supports the recently proposed homology of the furcula with the interclavicle, instead of representing fused clavicles. Interclavicles were thus not lost, but may have remained cartilaginous or have yet to be found in basal dinosauriforms.

Abstract We report here new and the first mammaliamorph tracks from the Early Cretaceous of Africa. The tracksite, that also bears crocodylomorph and sauropod dinosaurian tracks, is in the Catoca diamond mine, Lunda Sul Province, Angola. The mammaliamorph tracks have a unique morphology, attributed to Catocapes angolanus ichnogen. et ichnosp. nov. and present an anterolateral projection of digit I and V. The tracks with an average length of 2.7 cm and width of 3.2 cm are the largest mammaliamorph tracks known from the Early Cretaceous unmatched in size in the skeletal fossil record. The crocodylomorph trackways and tracks are attributed to Angolaichnus adamanticus ichnogen. et ichnosp. nov. (‘ichnofamily’ Batrachopodidae) and present a functionally pentadactyl pes, an extremely outwardly rotated handprint, and an unusual tetradactyl and plantigrade manus. One medium-sized sauropod dinosaur trackway preserved skin impressions of a trackmaker with stride length of 1.6 m; a second is that of a small-sized sauropod trackmaker with a pace length of 75 cm.

The Upper Jurassic of Portugal has a rich vertebrate fauna well documented from both body and trace fossils. Although the occurrence of crocodyles and pterosaurs is well documented from body fossils, trace fossils from both groups were unknown until now. Here we describe an isolated crocodyle-like track from Praia da Peralta and pterosaur tracks from the Kimmeridgian of Pedreira do Avelino, Sesimbra (Azóia Fm.) and Porto das Barcas, Lourinhã (Lourinhã Fm.). An enigmatic track suggests the possible presence of a small, tail-dragging tetrapod.
Possible track-makers are suggested based on the known Late Jurassic vertebrate fauna of Portugal.

A partial sauropod was found in 1996 in Vale Pombas, north of Lourinhã, Central West of Portugal, in the Lourinhã Formation, top of Amoreira Porto Novo member dated as c. 150 M.a. (Early Tithonian, Late Jurassic) and is currently housed at Museum of Lourinhã, in Portugal. The specimen (ML368) comprises a complete tooth with root, anterior chevron and almost complete right forelimb including partial scapula, complete coracoid, humerus, ulna, radius, metacarpals I, III and V, phalanx, and ungual phalanx I. It can be ascribed to Turiasaurus riodevensis, which was previously described from the Villar del Arzobispo
Formation at Riodeva (Teruel, Spain). Characters shared with T. riodevensis holotype include: curvature and asymmetry of tooth crown, expansion of crown, outline of humerus, medial deflection of the proximal end of humerus, shape and prominence of deltopectoral crest, vertical ridge in the distal half of the ulna (considered as diagnostic of Turiasauria), configuration of metacarpals, and bone proportions. It differs from T. riodevensis holotype by the smaller size and the more rectangular ungual phalanx in lateral view. The sediments from which the Riodeva specimen was recovered were previsouly thought to be Tithonian to Berriasian in age. The presence of this species in Portugal, in beds confidently dated as Early
Tithonian, may allow a more precise date for the Riodeva type locality of early Tithonian in age. The humerus of the Portuguese T. riodevensis is 152 cm long. Although shorter than the Spanish specimen (790 mm), it represents a large individual. All adult sauropods recovered in Portugal thus far are very large individuals: Dinheirosaurus (estimated body length is 20-25 m), Lusotitan (humerus length estimated to be 205 cm), Lourinhasaurus (femur length: 174 cm), and Turiasaurus here reported. The lack of of small or medium adult body-size sauropods in the Late Jurassic of Portugal, suggests browsing niches thought to be occupied by smaller forms, could be have been available for other dinosaurs, like the long necked stegosaur Miragaia longicollum.

The Late Jurassic Lourinhã Formation contains a diverse dinosaur fauna comprising theropods, sauropods, stegosaurs, ankylosaurs and several genera of ornithopods.
The sedimentology in the area favours preservation of footprints, and footprints from most of the dinosaurs represented by skeletal remains are present in the area. During fieldwork in the summer of 2003 a new, large, tridactyl footprint was found at the beach of Vale Frades, approximately 6 km north of Lourinhã, Portugal. The footprint was found together with a stegosaur footprint on a clay bed exposed within the tidal zone. The footprints were preserved as sandstone casts standing on a pedestal of clay. This unusual type of preservation is the result of the footprints having first been emplaced in clay, and then filled with sand. During the present day erosion from the sea, the harder sandstone cast of the footprints protects the subjacent clay layers from erosion. Owing to the immediate danger of erosion of, the footprint was collected and is now on display at Museu da Lourinhã (ML 1000). The footprint is 70 cm long and 69 cm wide, the toes are short and broad, with indications of short blunt claws. The

divarication angle between the outer digits is close to 90 degrees. The dimensions and general

morphology of the footprint identifies it as deriving from an ornithopod dinosaur with an estimated hip height of 4.13 metres. Although very large ornithopods are known from the Cretaceous, the largest known Jurassic ornithopod is Camptosaurus from USA, and the largest known from Portugal is the camptosaurid Draconyx loureiroi. Neither of these reached the body size suggested by the new footprint. So far the footprint described herein is s the only evidence for a Jurassic ornithopod of that size.

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Dinosaurs and other fossils have been artificially enhanced, or totally forged, to increase their commercial value. The most problematic forgeries to detect are based on original fossils that are artificially assembled. Several techniques are suggested for detecting hoaxes: detailed visual examination, chemical analysis, Xray or CT-scan, and ultraviolet light. It is recommended that museums and paleontological researchers do not purchase and/or trade fossils lacking clear provenience information. Exceptions to that general rule should be closely examined using techniques described herein.

The basal part of the Triassic-Jurassic (Rhaetian-Sinemurian) Kap Stewart Formation, exposed at Jameson Land, East Greenland, yields an extensive coprolite collection from black, parallel-laminated mudstone (“paper shale”), representing an open lacustrine system. Preliminary investigations show three different types of coprolites: elongated cylindrical masses, composed of irregularly wrapped layers; elongated cylindrical masses with constriction marks; and spirally-coiled specimens.

Late Jurassic theropod dinosaurs have been known in Portugal since 1863 but only now are they being fully understood, with the recognition of genera such as Allosaurus, Aviatyrannis, Ceratosaurus, Lourinhanosaurus, and Torvosaurus from the Lourinhã and Alcobaça Formations (Kimmeridgian/Tithonian). Ceratosaurus dentisulcatus can now be reported from Portugal. It represents the only occurrence of this species outside the Morrison Formation.
New cranial elements confirm the presence of Torvosaurus tanneri, in Portugal. Torvosaurus was the largest Late Jurassic land carnivore. New postcranial and cranial elements allow the erection of a new species from Portugal, Allosaurus europaeus n.sp. The theropod assemblage of Portugal is similar to that of the Morrison Formation.

A portion of a left humerus from the Upper Maastrichtian of Vratsa district (NW Bulgaria)
is shown to be from a non-avian theropod dinosaur: this is the first record of a
dinosaur from Bulgaria. We describe this bone, suggest that it most likely pertains to an
ornithomimosaur, and discuss the fossil record of other similar taxa of Late Cretaceous
age that have been reported from Europe. To investigate the taphonomy of this fossil,
rare earth element (REE) analysis is combined with strontium (Sr) isotope data to confirm
that this Bulgarian dinosaur bone was initially fossilized in a terrestrial environment,
then later re-worked into late Maastrichtian marine sediments.

Upper Jurassic nesting site from Paimogo (Lourinhã, Portugal) yielded the oldest dinosaur theropod embryos ever found. Numerous bones, including skull bones, from the skeleton of these embryos have been collected. The study of bones and embryos offers the possibility to learn more on the early life of theropod dinosaurs.

Africa is the only continent that now straddles arid zones located beneath the descending limbs of both the northern and southern Hadley cells, and it has done so since it became a distinct continent in the Early Cretaceous. Since that time, Africa has drifted tectonically some 12 degrees north and rotated approximately 45 degrees counterclockwise. This changing latitudinal setting and position of the landmass under the relatively stable Hadley Cells is manifested as southward migration of climatic zones over the past 132 million years. Data from kerogen, X-ray diffraction analysis of sedimentary matrix, carbon isotopes from shell samples and tooth enamel,new 40Ar/39Ar radiometric dates, pollen and plant macrofossils, and fossil vertebrates indicate a productive upwelling system adjacent to a coastal desert since the opening of the South Atlantic Ocean; however, the position of the coastal desert has migrated southward as Africa drifted north, resulting in today's Skeleton Coast and Benguela Current. This migration has had a profound effect on the placement of the West African coast relative to areas of high marine productivity and resulting extensive hydrocarbon deposits, on the placement of arid zones relative to the continent especially the Skeleton Coast desert, on the climatic history of the Congo Basin (which shows a Late Cretaceous decrease in aridity based on the relative abundance of analcime in the Samba core), and in reducing the southern temperate region of Africa from 17{%} of continental area during the Cretaceous to 2{%} today. We show here that these related geographic and environmental changes drove ecological and evolutionary adjustments in southern African floras and faunas, specifically with respect to the distribution of anthropoid primates, the occurrence of modern relicts such as the gnetalean Welwitschia mirabilis, endemism as in the case of ice plants, and mammalian adaption to an open environment as in springhares. Africa's tectonic drift through climate zones has been a first-order environmental determinant since the Early Cretaceous.

Este capítulo apresenta uma visão geral da paleobiodiversidade alfa de Angola com base no registo fóssil disponível, o qual se limita às rochas sedimentares, a sua idade variando entre o Pré‑Câmbrico e o pre‑
sente. O período geológico com a maior paleobiodiversidade no registo fóssil angolano é o Cretácico, com mais de 80% do total dos táxones fósseis conhecidos, especialmente moluscos marinhos, sendo estes na sua maioria
amonites. Os vertebrados representam cerca de 15% da fauna conhecida e cerca de um décimo destes são espécies descritas pela primeira vez com base em espécimes de Angola.

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A survey of Hemidactylus turcicus (Reptilia, Gekkonidae) was carried out every 3 weeks from March to November of 1997, in nocturnal transects in the city of Évora, Portugal. In this country this species is strictly nocturnal with a mean daily activity peak at 2hOO A.M (UTC).A model that correlates Activity and Temperature of the air is given. H. turcicus prefers, as microhabitat, walls (78%) and doors (16%) of low used houses. The average height in which they were found is about 3 meters.

Portugal has been providing dinosaur remains since, at least, 1863. The 18th century tiles depicting the legend of Our Lady in Cabo Espichel are probably the oldest known dinosaur track illustration. To our knowledge, the first remains found in Portugal were theropod teeth collected near Porto das Barcas (Late Jurassic of Lourinhã) in June 20th, 1863 by the geologist Carlos Ribeiro (1813-1882). The first dinosaur paper was written by Henri Sauvage (1842-1917) published in 1896. All remains collected since 19th century were gathered in a work signed by Albert de Lapparent (1905-1975) and Georges Zbyszewski (1909-1999 ) titled Les Dinosauriens du Portugal (1957) that was a significant milestone in the Portuguese dinosaur paleontology and gives the state-of-the-art by the time. Several dinosaurs are named, described, depicted and mapped in that monograph. The first track record is given by Jacinto Pedro Gomes (1844-1916) in 1916. Concerning the non-scientific literature referring to dinosaurs, in 1884 the newspaper Occidente reports the Bernissart findings in Belgium. In the 1959 occurs the first visit to Portugal of Walter Kühne (1911-1991) from the Free University of Berlin. Further visits and work granted the access to the Guimarota Mine and other Late Jurassic deposits in the 1960’s, 70’s and 80’s with a high number of publications. In the 1980’s and early 1990’s starts a progressive era for dinosaur paleontology in Portugal with the works of Peter Galton, Miguel Telles Antunes, the Natural History Museum, the Museum of Lourinhã and the New University of Lisbon, Oliver Rauhut, and others.