965 resultados para Cretaceous-Miocene stratigraphy


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This contribution summarizes the biostratigraphy of planktonic foraminifers, calcareous nannofossils, and benthic foraminifers, in combination with the magnetostratigraphy, carbon and oxygen isotope stratigraphy of benthic foraminifers, and CaCO3 stratigraphy for the Maestrichtian through Paleogene calcareous sequences recovered at Sites 689 and 690 on Maud Rise (at about 65°S, eastern Weddell Sea, Antarctica). These data represent the southernmost calciumcarbonate record available for that interval, and thus extend the biostratigraphic and isotopic database to higher latitudes. Sites 689 and 690 form the southernmost anchor of a north-south transect through the Atlantic Ocean for Paleogene biostratigraphy and chemostratigraphy.

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The sedimentary record of the Tarcău and Vrancea Nappes, belonging to the flysch accretionary zone of the Eastern Carpathians (Eastern Carpathian Outer Flysch), registered Cretaceous-Miocene events during the evolution of the Moldavidian Basin. Our biostratigraphic data indicate that the deposits studied are younger than previously reported. The comparison of sedimentary record studied with the Late Cretaceous-Early Miocene global eustatic curve indicates that eustatic factor played a secondary role, after the tectonic one. Four main stages of different processes influenced by tectonics are recognized in the sedimentary record: (1) Campanian-Maastrichtian-earliest Paleocene; (2) latest Ypresian-Lutetian; (3) late Chattian-earliest Aquitanian, and (4) late Aquitanian-early Burdigalian. The late Chattian- earliest Aquitanian and late Aquitanian-early Burdigalian records indicate a high tectonic influence. The first event was related to the foredeep stage of the sedimentary domain studied, and the second one to the deformation stage of the same domain. The sedimentary records of tectonic influence recognized during these stages are useful tools for geodynamic reconstructions. The stratigraphic correlation of Tarcău and Vrancea sedimentary records are used

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The Aquitaine Basin (southwestern France) is known since long ago for its richness in marine miocene deposits of various facies. A few stratotypes concerning this period have been described in the investigated area. The stratigraphical framework has been 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 (larger 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 allowed 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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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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Since the XIX century, Portuguese and foreign geologists have defined 47 new invertebrate taxa (foraminifera, ostracods, coelenterates, brachiopods, gastropods, ammonoids, echinoids), 2 new fossil plant taxa (charophyte and pteridophyte) and 1 ichnofossil, using toponymy from the Algarve; these taxa refer to 1 genera, 47 species and 2 varieties. Besides the Algarve toponym, the most used as specific name, twenty others have been used, mostly from western Algarve; these toponyms are associated to: – Miocene units, particularly from Ribeira de Cacela and Ferragudo; – Cretaceous units between Zavial and Marim; – Upper Jurassic units from Sagres, Carrapateira and Loulé and Middle Jurassic units from Sagres and Guilhim; – Triassic units from Vila do Bispo to Tavira; – Carboniferous units, particularly from the Aljezur-Bordeira-Carrapateira region. The earliest of these designations were attributed to seven gastropods from the Upper Miocene of Cacela (COSTA, 1866-1867). The majority of the named species are typical of the Algarve, but some have been collected, as well, in the Lusitanian Basin. Although extensively cited in the geological literature, some of these taxa either do not fulfill the ICZN rules, or fall into synonymy with previously established taxa, or should be formally considered as non valid names (nomem nudum and nomen oblitum). Only widespread bibliographical review, associated with the palaeontological revision of some of these groups and the correct interpretation of the ICZN articles, will allow confirming, or not, the doubts that have now arisen.

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The endemic stingless honey-making bee Melipona (Melikerria) insularissp.n. on Coiba and Rancheria Islands in Pacific Panama is described, together with the proposed sister species, M. ambigua sp.n. from northeast Colombia. The Coiba Island group and Panama mainland were surveyed, yielding one meliponine endemic (M. insularissp.n.) and six meliponine genera and species. The poor Coiba fauna of amphibians and birds corresponds to the poor social bee fauna and suggests habitat barriers generally precluded recolonization from the mainland during glacial periods. Many animals became extinct, yet some remain as relicts. Melipona insularissp.n. was isolated on accreted terranes of Coiba rainforest in the Panama microplate. Morphology suggests that M. insularissp.n. is not a direct descendant of the San Blas-E. Panama endemic Melikerria, M. triplaridis. A phylogenetic hypothesis corroborates disjunct distributions. Rainforest endemics such as Peltogyne purpurea (Fabaceae) and Ptilotrigona occidentalis (Apidae, Meliponini) also occur as relictual, disjunct populations in Central and South America. These may have been isolated before accelerated biotic exchange began 2.4 Ma. Our work supports the geological findings of both a volcanic arc and the San Blas massif providing a substantial bridge for Melikerria from Colombia and Panama in Eocene to Miocene times. We suggest there have been taxon cycles permitting recolonization during glaciations, whereby colonies of M. insularissp.n. were able to recolonize Rancheria, a 250 ha island, 2 km from Coiba. However, rafting colonies nesting in trees, carried on vegetation mats, may have produced founding populations of Melipona in Central America and on oceanic islands such as Coiba.

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Estudios estratigráficos y sedimentológicos de afloramiento y el análisis paleoecológico y bioestratigráfico mediante foraminíferos, han permitido realizar una reinterpretación sedimentaria de las unidades de margas y areniscas miocenas del sector nororiental de la Cuenca del Guadalquivir. El relleno sedimentario ha sido dividido en cuatro unidades litoestratigráficas (I-IV), todas ellas depositadas durante el Tortoniense, entre 10 y 7.89 Ma, aproximadamente. La Unidad I (Tortoniense antiguo no basal) está fomada por arenas y calizas de algas, y es interpretada como una unidad transgresiva y expansiva sobre el basamento que evoluciona desde ambientes marinos someros a rampa de carbonatos tipo rhodalgal. La Unidad II (Tortoniense inferior, biozona MMi11: entre 10 y 9.54 Ma) está caracterizada por una alternancia rítmica de margas arcillosas y silíceas, depositadas en ambientes pelágicos y profundos de aguas frías-eutróficas, si bien con repetidos cambios en la estratificación y distribución de nutrientes en la columna de agua. Esta unidad registra una importante somerización en su parte superior, dando paso gradual a la Unidad III. La Unidad III (Tortoniense inferior, biozonaMMi11: desde 9.54 Ma) está dominada por areniscas, aunque lateralmente aparecen brechas intraformacionales con estratos contorsionados. Está nutrida por deltas desde la costa y se interpreta como el depósito de bancos arenosos movilizados por la acción de corrientes mareales y el oleaje de tormentas en rampas. La Unidad IV (Tortoniense superior, biozona MMi12: desde 8.35 Ma) está representada por margas pelágicas similares a las de la Unidad II, de la que difiere por la presencia de intercalaciones arenosas genéticamente relacionadas con procesos mareales y de tormentas.