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The diversity of fossil crocodylomorphs in Portugal is high, with occurrence as old as Mystriosaurus (=Steneosaurus) bollensis from the Lower Jurassic. The Late Jurassic forms are the better documented, and include the following taxa: Machimosaurus hugii, Lisboasaurus estesi Seiffert, 1973, Lusitanisuchus mitrocostatus Seiffert, 1975; Schwarz & Fechner 2004, Theriosuchus guimarotae Schwarz and Salisbury 2005, Cf. Alligatorium, Goniopholis baryglyphaeus, and a crocodylomorph-like eggs in dinosaur nests (Mateus et al., 1998; Ricqlès et al., 2001). From the Lower Cretaceous were reported a few dinosaurs but its record is strangely scarce in crocodylomorphs (Mateus et al., 2011). The Upper Cretaceous crocodiles show a large diversity, but it is mostly based in fragmentary material that require revision, such as “Crocodylus” blavieri? Grey from the Upper Campanian - Maastrichtian of Viso, near Aveiro (initially reported by Sauvage 1897-98), Goniopholis cf. crassidens Owen 1841 and Oweniasuchus pulchelus Jonet 1981. Moreover there is a fascinating, but poorly understood, crocodylomorph diversity in the Cenomanian of Portugal, documented by fragmentary specimens that have been doubtfully assigned to Thoracosaurus Leidy 1852 of the Middle Cenomanian of Cacém, to the nomen dubium Oweniasuchus lusitanicus Sauvage 1897-98 (interpreted as a mesosuchian goniopholid) based in a fragmentary mandible from the Campanian-Maastrichtian, and also from the Middle Cenomanian of Portugal, Buffetaut and Lauverjat (1978) report an fragmentary unidentified possible dyrosaurid from Nazaré. All this specimens are too incomplete to be compared with the specimen here described. In contrast, Cenozoic crocodiles of Portugal are often known after complete skulls and several individuals. The taxa list include Iberosuchus macrodon (Lower to Middle Eocene), Tomistoma calaritanus (Early Miocene) and T. lusitanica (Burdigalian-Helvetian), and Diplocynodon sp. (Antunes, 1961, 1987, 1994).
At least, two different morphotypes of crocodylomorph eggs from the Late Jurassic of Lourinhã Formation are also known.
A new specimen here reported of crocodile based in a partial skull and mandible (ML1818) from the Uppermost Middle Cenomanian platform carbonates of Baixo Mondego, west central Portugal (Tentúgal Fm., Callapez, 2004). The taxon is phylogenetically positioned as a basal Eusuchia, due to the choanae enclosed by the pterygoid, and closely related with stem Crocodylia and Borealosuchus. This specimen represents the only well documented and valid eusuchian species in the Cenomanian of Europe and is the oldest representative of an eusuchian crocodylomorph, with the exception for the Barremian Hylaeochampsa vectiana.

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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.

Despite more than a century of collecting, resulting in one of the best-studied vertebrate fossil records anywhere in the world, the Upper Jurassic Morrison Formation has produced surprisingly few examples of dinosaur eggs associated with embryonic remains. Even more puzzling, none of these seem to pertain to the theropod Allosaurus, one of the most common and best-understood dinosaur taxa in the formation. Here we report on a dinosaur nest site that has produced both abundant prismatoolithid eggshell and embryonic (or perinatal) bones of Allosaurus from Fox Mesa, Wyoming. This represents the first such discovery for any theropod in the Jurassic of North America. The nest is heavily weathered but contains a few ellipsoid eggshell clusters that suggest an egg size of about 8 x 6.5 cm. Study of the eggshell morphology and microstructure confirms that a single egg type is present throughout, which is indistinguishable from Prismatoolithus coloradensis. All of the identifiable embryonic materials pertain to theropods, and two premaxillae specimens show the five alveoli diagnostic for Allosaurus among Morrison theropods. This confirms the theropod origin of Prismatoolithus eggs and implicates Allosaurus as the specific Morrison parent taxon. As a result, it is now possible to assign several previous discoveries of dinosaur eggs and potential nests to Allosaurus, including the isolated egg from the Cleveland-Lloyd Quarry. This discovery also calls into question prior assignments of Prismatoolithus eggs to ornithopods, and suggests that more detailed study of such sites is warranted. Prismatoolithus eggshells are also associated with the Upper Jurassic theropod Lourinhanosaurus from Portugal, along with larger embryos that exhibit four premaxillary alveoli.

A single, geographically and temporally restricted horizon at Bentiaba, Angola (14.3° S), preserves a concentration of skeletons and isolated elements representing sharks, rays, bony fish, at least three species of turtles, two species of plesiosaurs, at least five species of mosasaurs, and rare volant and terrestrial forms. The concentration, referred to as the Bench 19 Fauna, formed on a narrow continental shelf at paleolatitude 24°S as predicted by paleomagnetic data and confirmed by plate motion models. The shelf evolved as a transform passive margin along faults associated with the opening of the South Atlantic. Latitude 24°S falls today along the coast of northern Namibia, an area of intense upwelling and hyperarid coastal desert. The Namibe Basin in southern Angola is separated from the Walvis Basin of Namibia by the Walvis Ridge, and the continental shelf in northern Namibia is eight times the width of that at Bentiaba. However, the sediment entombing the fossils at Bentiaba is an immature feldspathic sand, shown by detrital zircon ages to be derived from nearby exposed granitic shield rocks, suggesting similar climatic and drainage conditions between the two regions. Temporal control of the Bentiaba section is provided by magnetostratigraphy and stable carbon isotope chemostratigraphy anchored by an Ar40/Ar39radiometric date on basalt. The age of Bench 19 is constrained to chron C32n.1n and thus falls between 71.4 and 71.64 Ma. Massive bedding without hummocky cross-bedding or other sedimentary structures indicates deposition in shallow water below wave base. δ18O analysis of bivalve shells indicates a water temperature of 18° C immediately below Bench 19. Nearest neighbor distance peaks at 5 m (n=19

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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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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.