999 resultados para Mare de Déu dels Desemparats-Culte-València-Història


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The Aquitaine Basin (southwestem France) is known since long ago for its richness in marine miocene deposits ofvarious facies. A few stratotypes concerning this period have bccn described in the investigated area. The stratigraphical framework has becn recently revised and the study of new exposures completes our knowledge on these levels. In the present work, the authors produce a biostratigraphical distribution of about 160 species (Iarger and smaller foraminifera), found in the surface exposures of Aquitaine, from the topmost Oligocene (Chattian) through to Middle Miocene (including Serravallian). As a rule, the common species without significant ranges have not bcen mentioned. The microfaunas of several exposures have been thoroughly revised, which has allowcd to precise the distribution of many species and induced a few modifications of the results previously produced. Synonymy problems and new taxonomical revisions have been taken into account. Of course, this work will be probably submitted to some changes according to new research on the already known exposures or other more recently discovered.

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Abundant crops of Glycymeris have been made in the neritic bioclastic deposits of the Aquitaine Basin. After an outline about the Chattian taxa, the 5 Lower Miocene lineages are presented; G. cor is plainly predominant. Then, the Middle Miocene faunas are also detaiIed, G. inflatus and G. bimaculatus being the most frequent taxa. A test of biometrical analysis about the G. cor species is presented.

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Proceedings of the I" R.C.A.N.S. Congress, Lisboa, October 1992

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A rich uppermost Miocene selachian fauna from the Alvalade Basin (represented by more than 10.000 teeth) is accounted for. It is the most modern miocene fauna of neritic habit under warm-temperate to subtropical conditions, known in the european Miocene.

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Similarly to other organisms, Vertebrates changed during the Cenozoic Era. Mammals are the only ones to change quickly; their well mineralised bones and teeth are often fossilised. They are highly diverse and even isolated teeth can be identified. They are thus a good tool for establishing a biochronological framewoork. Among Mammals, Rodents with a short lifetime evolve more quickly than the large Mammals. In Europe, the first elaborated zonation was investigated by the Regional Committee on Neogene Stratigraphy and issued as the MN Zonation (Mammals Neogene) by Mein, 1976. During the following years, progress in knowledge lead to new charts. The latest one resulted from collective work (de Bruijn et al., 1992). Bîochronology gives relative data; if we desire to have numerical age estimates, we must correlate these results with radiometrie data, marine biostratigraphîcal units or the Geomagnetic Polarity Time Scale. For Europe, these results are summarised by Steininger et al. (1989-1996) and Steininger (1999). After some recents developments on MN Zonation, here is discussed the succession of Neogene small mammals Portuguese localities. Fortunately these localities are in majority inbedded in marine context. Their assigment to MN Zones is proposed and correlations with the spanish Aragonian Scale (Daams el al., 1999) are also suggested. In fact, some differences appear between Portugal and Aragonian assemblages, probably for ecological reasons. Therefore, the MN zonation is always useful for short and long distance biochronological correlations.

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New data led us to revise Miocene Perissodactyla from Lisbon. Equids (Anchitherium) have been decribed by Alberdi & González (1999); we fully agree with their conclusions. On the other hand, the only Chalicotheriid cannot be clearly reported to any genus. It therefore will be left in open nomenclature Schizorheriinae ind.). The Rhinocerotids have been described in detail (1983). We could recognize now that: Protaceratherium sagicum is a synonym of P. minutum; Plesiaceratherium platyodon and Plesiaceratherium lumiarense should be ascribed to the genus Plesiaceratherium and not to Aceratherium; there are no reasons for name changes as far as the forms previously referred as Diaceratherium aurelianensis, Prosantorhinus germanicus and Hispanotherium matritensis are concerned; as the genera Dicerorhinus and Lartetotherium are distinct, Dicerorhinus (Lartetotherium) sansaniensis has to be named Lartetotherium sansaniensis; as Gaindatherium (Ïberotherium) rexmanueli cannot be reported to Gaindatherium, we therefore upgrade the subgenus Iberotherium to the genus'rank - hence the names of the concerned taxa become Iberotherium rexmanueli rexmanueli and I. rexmanueli zbyszewski; Chilotherium ibericus is but a dental variation of I. rexmanueli zbyszewski. The stratigraphic distribution and age of the Miocene Perissodactyla so far known in the Lower Tagus basin / Lisbon region are presented.

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Discovery of a fifth metapodial of the Creodont Hyaenodontidae Hyainailouros sulzeri at Quinta da Farinheira (Chelas), near Lisbon (Portugal) in the beginning of the Middle Miocene.

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The Domerian sections from the Lusitanian Basin of São Pedro de Muel, Rabaçal and Tomar have provided us with more than 1100 Ostracods belonging from 18 genus and about 48 species. The faunal diversity and density of the associations decrease in space (from Tomar to Rabaçal and São Pedro de Muel) and time, with favourable environments for the proliferation of Ostracods at the lower part of the sections (Stokesi subzone) and more hostile at the upper part (Ragazzonii subzone). The Monestieri and Nitescens horizons and the Subnodosus subzone are characterized by a typical assemblage of Ostracods. The palaeoecological Ostracod indexes reveal the fluctuations of the oxygenation, temperature, depth and hydrodynamism of the water, on the different sections and on the whole platform. They display a diachronous cooling in the Lower Domerian series. In the upper part of the Middle and in the Upper Domerian, the deeper, less oxygenated and cooler waters prevent the development of the Ostracod faunas.

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Fragmentary skeletal remains of Percoid fishes (Teleostei, Percoidei) are described from the Upper Paleocene? or Lowermost Eocene(MN7) from Silveirinha. It is suggested that they belong to some primitive Percoids which are already known in the Iberian peninsula. They bear witness of an ancient westwards extension of the geographical distribution of Percoid fishes that are common in the lower levels of the Eocene in the Douro Basin in Spain.