524 resultados para Chiasmolithus eograndis


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During Ocean Drilling Program Leg 171B, a thick sequence of lower to middle Eocene sediments was recovered from Sites 1051 and 1052 at Blake Nose in the North Atlantic Ocean. Calcareous nannofossils are moderately well preserved in the upper to middle Eocene sediments but are moderate to poorly preserved in the lower Eocene sediments. Calcareous nannofossils are diverse throughout the recovered sequence, which extends from nannofossil Zone CP8 to Subzone CP15a. The nannofossil biostratigraphy of these sites indicates the presence of a hiatus in Subzone CP12a in the middle Eocene, in which the major nannofossil assemblage changes dramatically from Toweius to reticulofenestrid; however, no major change in the nannoflora was observed across the Eocene/Paleocene boundary. Coccolith size evolution patterns were recognized. Coccolithus, Reticulofenestra, and Cribrocentrum specimens may suggest a trend of increasing size upward through the sedimentary sequence, but Dictyococcites does not show a similar simple trend. Most traditional zonal markers are present. The reworking of Discoaster sublodoensis and overgrowth of Tribrachiatus in the lower Eocene makes zonal subdivision of this part of the sequence difficult. For this reason, tentative nannofossil zonation is given for the lower Eocene.

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During Leg 110 of the Ocean Drilling Program, sediment was recovered from six sites in the vicinity of the Lesser Antilles Forearc. Hole 671B, drilled near the toe of the Barbados deformation front, was the first-ever penetration of the decollement between the underthrusting Atlantic Plate and the off scraped Barbados accretionary prism. Stratigraphic repetitions in sequence associated with tectonic movement along the decollement zone, first observed on DSDP Leg 78A, were further documented at four ODP Leg 110 sites. A significant biostratigraphic inversion is present at Site 671 at 128 mbsf in which upper Miocene sediments rest atop lower Pleistocene strata. Smaller repetitions in sequence are recorded at Sites 671, 673, 674, and 676. Leg 110 sediments range from middle Eocene to early Pleistocene in age. Pliocene/Pleistocene assemblages are generally well preserved; however, Miocene assemblages have undergone extensive dissolution at all Leg 110 sites. Paleogene sediments are sometimes recrystallized and the nannofossils contained within exhibit a range in preservation from poor to good.

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This work presents the stratigraphic distribution of several species of calcareous nannofossil in the middle Eocene early-Oligocene from four Ocean Drilling Program (ODP) sites located between 60° and 65°S paleolatitude in the Southern Atlantic and Indian Oceans. Useful nannofossil datums that should facilitate construction of age-models and contribute to an integrated chronology for the upper Paleogene Southern Ocean sediments from ~42 to 33 Ma are summarized. The distribution patterns of calcareous nannofossils, studied by means of quantitative and semiquantitative methods, provide an improvement of the classical Southern Ocean biozonations, introducing new biostratigraphically useful biohorizons, and testing their reproducibility within and outside the region.

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In the collective monograph results of geological and geophysical studies in the Tadjura Rift carried out by conventional outboard instruments and from deep/sea manned submersibles "Pisces" in winter 1983-1984 are reported. Main features of rift tectonics, geology, petrology, and geochemistry of basalts from the rift are under consideration. An emphasis is made on lithology, stratigraphy, and geochemistry of bottom sediments. Roles of terrigenous, edafogenic, biogenic, and hydrothermal components in formation of bottom sediments from the rift zone are shown.

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Positions of all cores recovered during Ocean Drilling Program (ODP) Leg 112 off Peru are shown in the standard calcareous nannoplankton zonation. Stratigraphic and regional occurrences and preservation of calcareous nannoplankton are discussed for all sites, and fossil lists are presented for selected samples. Late Miocene to Holocene nannoplankton assemblages in the upwelling systems off Peru and scattered blooms, especially of Gephyrocapsa species and Helicosphaera carteri, are described. Scyphosphaera assemblages found in late Miocene Zone NN9 {Discoaster hamatus Zone) at Site 684 are compared with similar assemblages from Gabon on the west coast of Africa. Remarkable subsidence is indicated by early and middle Eocene nearshore and shallow-water nannoplankton assemblages for Sites 682, 683, and 688. Besides several local hiatuses, major regional hiatuses were noted at Site 682 (upper Eocene, uppermost middle Eocene, and part of the lower and middle Oligocene missing), Site 683 (uppermost middle Eocene to lower part of the middle Miocene missing), and Site 688 (part of the middle Eocene, uppermost middle Eocene to upper Oligocene, and parts of the lower and middle Miocene missing).

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Seven sites were drilled off the eastern shore of New Zealand during Ocean Drilling Program Leg 181 to gain knowledge of southwest Pacific ocean history, in particular, the evolution of the Pacific Deep Western Boundary Current (DWBC). Holes 1123C and 1124C penetrated lower Oligocene to middle Eocene sediments containing moderately to poorly preserved calcareous nannofossils. Nannofossil assemblages show signs of dissolution and overgrowth, but key marker species can be identified. Nannofossil abundance ranges from abundant to barren. The lower Oligocene sediments are distinctly separated from the overlying Neogene sequences by the Marshall Paraconformity, a regional marker of environmental and sea level change. An age-depth model for Hole 1123C through this sequence was constructed using nine nannofossil age datums and three magnetostratigraphic datums. There is good agreement between the biostratigraphy and magnetostratigraphy, which indicates that the Marshall Paraconformity spans ~12 m.y. in Hole 1123C. The same sequence in Hole 1124C is disrupted by at least three hiatuses, complicating interpretation of the sedimentation history. The Marshall Paraconformity spans at least 3 m.y. in Hole 1124C. A 4- m.y. gap separates lower Oligocene and middle Eocene sediments, and a ~15 m.y. hiatus separates middle Eocene mudstones from middle Paleocene nannofossil-bearing mudstones. Nannofossil biostratigraphy from Holes 1123C and 1124C indicates that the Eocene-Oligocene transition was a time of fluctuating biota and intensification of the DWBC along the New Zealand margin.

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A high-resolution calcareous nannofossil analysis of the Danian/Selandian boundary was conducted at Site 1262 (Walvis Ridge, South Atlantic) to pinpoint the lowest occurrence of fasciculiths and to unravel the evolutionary trends throughout nannofossil Zone NP4. Using quantitative analyses, numerous primary and secondary bioevents were identified, improving the biostratigraphic resolution of this interval. The main events recorded at Site 1262 were also identified at the Zumaia section Global Stratotype Section and Point (GSSP) of the base of the Selandian and at the Qreiya section (Egypt). The lowest occurrence of fasciculiths (represented by the LO of Gomphiolithus magnicordis and Gomphiolithus magnus) was observed in the middle part of Chron C27r, above the LO of Toweius pertusus and prior to the LO of the genus Sphenolithus. The synchroneity of the LO of fasciculiths was also verified at various latitudes, such as DSDP Site 384 (NW Atlantic), ODP Site 761B (Indian Ocean) and DSDP Site 577A (Pacific Ocean). The first and second diversification events (Steurbaut and Sztrákos, 2008, doi:10.1016/j.marmicro.2007.08.004), or radiation events (Bernaola et al., 2009, doi:10.1344/105.000000272), of fasciculiths have been thoroughly discussed and well characterized by a succession of events. The occurrence of the Latest Danian Event (LDE) and several paleoenvironmental changes recognized during this time interval, coupled with an ecological competition with Sphenolithus, appear to be the probable causes of the First and Second Radiations and the fasciculith barren interval between them. The occurrence of new morphostructures and taxa suggests evolutionary trends and a strict link between morphological evolution and paleoclimate.

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Three of the six DSDP Leg 77 sites drilled in the western approaches to the Straits of Florida yielded thick sequences of Cenozoic sediment rich in calcareous nannofossils. Hiatuses are prominent in each of these continuously cored intervals. A prominent upper Oligocene hiatus, observed at each of these three sites, can be correlated to a large-scale "global" regression event. Other disconformable horizons present in the study area cannot be positively related to sealevel fluctuations and may be caused by a number of factors including local tectonic activity. Paleogene sections are generally marked by thick accumulations within the upper Oligocene Sphenolithus ciperoensis Zone and by a pronounced braarudosphaerid-holococcolith bloom recorded in the lower Oligocene and upper Eocene. This bloom is particularly well developed at Site 540. All samples examined contain abundant nannofossils. Preservation fluctuates throughout the sections from good to poor.

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Calcareous nannoplankton biostratigraphy has been worked out in the eastern Mediterranean utilizing deep-sea sediments recovered from DSDP Leg 42A Sites 375 and 376. These two drill sites were located approximately 55 km west of Cyprus on the Florence Rise. Sediments, ranging in age from early Miocene (Helicosphaera ampliaperta Zone) through Holocene, contain sufficient age-diagnostic species to recognize essentially all of the lowlatitude nannoplankton zones described by Bukry, although regional, secondary marker species are needed to define some zonal boundaries. Reworked Cretaceous and Paleogene nannoplankton occur throughout the stratigraphic interval studied, but not in quantities large enough to mask indigenous species. Sedimentation rates at Sites 375 and 376 were highest in the late Miocene and late Pleistocene. Open-marine, warm-water species of discoasters are present in significant numbers throughout the Miocene and Pliocene. Earliest Pliocene assemblages contain numerous specimens of ceratoliths. Nannoplankton in post-Messinian sediments at the drill sites and the Zanclean stratotype at Capo Rossello, Sicily, indicate that the base of the Amaurolithus tricorniculatus Zone (base of Triquetrorhabdulus rugosus Subzone) corresponds with the Miocene-Pliocene boundary.