819 resultados para Achradina pulchra


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The continuously influence of human impacts on the seafloor and benthic habitats demands the knowledge of clearly defined habitats to assess recent conditions and to monitor future changes. In this study, a benthic habitat dominated by sorted bedforms was mapped in 2010 using biological, sedimentological and acoustic data. This approach reveals the first interdisciplinary analysis of macrofauna communities in sorted bedforms in the German Bight. The study area covered 4 km², and was located ca. 3.5 km west of island of Sylt. Sorted bedforms formed as sinuous depressions with an east west orientation. Inside these depressions coarse sand covers the seafloor, while outside predominantly fine to medium sand was found. Based on the hydroacoustic data, two seafloor classes were identified. Acoustic class 1 was linked to coarse sand (type A) found inside these sorted bedforms, whereas acoustic class 2 was related to mainly fine to medium sands (type B). The two acoustic classes and sediment types corresponded with the macrofauna communities 1 and 2. The Aoinides paucibranchiata-Goniadella bobretzkii community on coarse sand and the Spiophanes bombyx - Magelona johnstonii community on fine sand. A transitional community 3 (Scoloplos armiger - Ophelia community), with species found in communities 1 and 2, could not be detected by hydroacoustic methods. This study showed the limits of the used acoustic methods, which were unable to detect insignificant differences in the fauna composition of sandy areas.

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Ocean Drilling Program Leg 103 occupied five sites on the Galicia margin, northwest of the Iberian Peninsula. Two holes (Holes 637A and 638B) yielded significant Cenozoic sedimentary sections ranging from late Miocene to late Pleistocene in age. From the nannofossil stratigraphy, one hiatus is recognized in Hole 637A (2.35-2.4 Ma), whereas two hiatuses (one at 1.9-2.6 Ma and another at 3.5-3.7 Ma) are recognized in Hole 638B. Sediment-accumulation rates for the Cenozoic portions of these two holes have been calculated based on the nannofossil datums. The abundance ratios of Coccolithus pelagicus to Discoaster brouweri for Hole 637A show relatively low values and small fluctuations from 2.5 to 6.5 Ma but sharply increase and then widely fluctuate beginning at about 2.5 Ma. This may indicate relatively warmer, more stable surface-water temperatures from 2.5 to 6.5 Ma and cooler, variable surface-water temperatures after 2.5 Ma at Site 637. C. pelagicus/D. brouweri ratios from Hole 638B also show a trend of increasing values with time from late Miocene to late Pliocene, but with more fluctuations and a different pattern from that of Hole 637A.

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To assess the paleoceanographic potential of Leg 186 sediments, we investigated Quaternary calcareous nannofossil flora at Sites 1150 and 1151 in the Japan Trench. Because of the frequent occurrence of barren intervals and the lack of oxygen isotope data, a detailed paleoceanography is not feasible for these cores. We limited our study to the upper 26.07 m of the section from Hole 1150A and the upper 21.01 m of the section from Hole 1151C. The studied samples from Cores 186-1150A-1H through 3H are younger than 0.085 Ma. Core 186-1151C-1H (upper 1.92 meters below seafloor [mbsf]) is younger than 0.085 Ma, and samples between 2H-7, 5-7 cm, and 3H-CC, 5-7 cm, (9.99-21.01 mbsf) are older than 0.245 Ma and younger than 0.408 Ma.

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The evolution of planktonic foraminifera during the Late Cretaceous is marked in the Santonian by the disappearance of complex morphotypes (the marginotruncanids), and the contemporary increasing importance and diversification of another group of complex taxa, the globotruncanids. Upper Turonian to lower Campanian planktonic foraminiferal assemblages from Holes 762C and 763B (Ocean Drilling Program, Leg 122, Exmouth Plateau, 47°S palaeolatitude) were studied in detail to evaluate the compositional variations at the genus and species level based on the assumption that, in the Cretaceous oceans as in the modern, any faunal change was associated with changes in the characteristics and the degree of stability of the oceanic surface waters. Three major groups were recognised based on gross morphology, and following the assumption that Cretaceous planktonic foraminifera, although extinct, had life-history strategies comparable to those of modern planktonics: 1 - r-selected opportunists; 2 - k-selected specialists; 3 - r/k intermediate morphotypes which include all genera that display a range of trophic strategies in-between opportunist and specialist taxa. Although planktonic foraminiferal assemblages are characterised by a progressive appearance of complex taxa, this trend is discontinuous. Variation in number of species and specimens within genera has allowed recognition of five discrete intervals each of them reflecting different oceanic conditions based on fluctuations in diversity and abundance of the major morphotypes. Planktonic forms show cyclical fluctuations in diversity and abundance of cold (r-strategists) and warm taxa (k-strategists), perhaps representing alternating phases of unstable conditions (suggesting a weakly stratified upper water column in a mesotrophic environment), and well-stratified surface and near-surface waters (indicating a more oligotrophic environment). Interval 1, middle Turonian to early Coniacian in age, is dominated by the r/k intermediate morphotypes which alternate with r-strategists. These cyclical alternations are used to identify three additional subintervals. Interval 2, aged middle to late Coniacian, is characterised by the increasing number of species and relative abundance of k-strategists. After this maximum diversification the k-strategists show a progressive decrease reaching a minimum value in Interval 3 (early to late Santonian), which corresponds to the extinction of the genus Marginotruncana. In the Interval 4, latest Santonian in age, the k-strategists, represented mainly by the genera Globotruncana, increase again in diversity and abundance. The last Interval 5 (early Campanian) is dominated by juvenile globotruncanids and r-strategists which fluctuate in opposite phase. The positive peak (Interval 2) related to the maximum diversification of warm taxa (k-strategists) in the Coniacian seems to correspond to a warmer episode. It is followed by a marked decrease in the relative abundance of warm taxa (k-strategists crisis) with a minimum in the late Santonian (Interval 3), reflecting a decrease in temperature. Detailed analysis of faunal variations allows the Santonian faunal turnover to be ascribed to a cooling event strong enough to cause the extinction of the marginotruncanids.

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A planktonic foraminiferal zonal scheme is presented for subdivision of the Upper Cretaceous pelagic carbonate sequence from southern mid-high latitudes. Definition of the zones is based on first and last occurrences of planktonic foraminifera from Ocean Drilling Program Holes 762C and 763B (Leg 122; Exmouth Plateau, south Indian Ocean). During the Late Cretaceous the studied holes were located close to 50°S and for the first time a complete sedimentary record for the mid-high latitudes was obtained. A detailed biostratigraphic analysis has allowed recognition of two new zones (Falsotruncana maslakovae Zone and Marginotruncana marianosi Zone) for the interval extending from the last occurrence of Helvetoglobotruncana helvetica to the first occurrence of Dicarinella asymetrica (upper Turonian - lower Santonian). From this study it is apparent that some low latitude (Globotruncana ventricosa, Hedbergella flandrini, Marginotruncana marianosi) and high latitude (Globigerinelloides impensus and Hedbergella sliteri) marker taxa display a vertical distribution at mid-high latitudes which is different from that known from low latitudes; moreover, one species (Heterohelix papula), overlooked at low latitudes, exhibits a restricted range that seems to be useful for chrono-biostratigraphic correlations: its appearance is suggested to coincide with the Coniacian/Santonian boundary. The proposed biozonation, which is integrated with calcareous nannofossil and magnetostratigraphic data available for the sections studied, is compared with both the low-latitude standard zonation and the planktonic foraminiferal zonal scheme for the circum-Antarctic region, in order to define a bio-chronostratigraphic scale that is useful for mid-high latitudes of the southern oceans.

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Rich radiolarian faunas were obtained continuously from Middle Jurassic to Lower Cretaceous radiolarite sequences at Sites 800 and 801, drilled during Ocean Drilling Program Leg 129 in the western Pacific. Occurrences of 90 taxa are presented in tables for these sites. Seven radiolarian zones, Dibolachras tytthopora, Cecrops septemporatus, Pseudodictyomitra carpatica, Pseudodictyomitra primitiva, Cinguloturris carpatica, Stylocapsa spiralis, and Tricolocapsa conexa in descending order, were recognized in this interval. The radiolarite sequences of Sites 800 and 801 encompass approximately the Berriasian to Hauterivian (or to Barremian) and the Bathonian/Callovian to Valanginian ages, respectively. At Site 801, a hiatus of early Oxfordian was identified.

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Leg 90 of the Deep Sea Drilling Project drilled 18 holes at eight sites (Sites 587-594) on several shallow-water platforms in the southern Coral Sea, Tasman Sea, and southwestern Pacific Ocean. The results from an additional hole (Hole 586B) drilled at Site 586 during Leg 89 are included in this report. Together, these sites form a latitudinal traverse which extends from the equator (Site 586) to 45°S (Site 594) and includes all the major water masses from tropical to subantarctic. Samples recovered at these sites range in age from middle Eocene to late Quaternary. The calcareous nannoplankton biostratigraphy for Leg 90 has divided into two parts: part 1, the Neogene and Quaternary of Sites 586-594. (this chapter); and part 2, the Paleogene of Sites 588, 592, and 593 (Martini, 1986). A slightly modified version of the Martini (1971) standard Tertiary and Quaternary zonation scheme was used to make age determinations on over 700 samples. All of the relevant Neogene and Quaternary zone-defining nannoplankton are present at Sites 586-591 (0°-30°S) but become increasingly rare or are absent at Sites 592-594 (35°-45°S). Species diversity increases southward from the equator (Site 586) and reaches a peak at 20°S (Site 587). A decrease at 25°S (Site 588) and 30°S (Sites 589-591) is followed by an increase in species diversity at 35°S (Site 592). South of 35°S, species diversity again decreases and reaches a low at 45 °S (Site 594). Species diversity for all sites as a group generally increases through the early, middle, and late Miocene, reaches a peak in the early Pliocene, then gradually decreases through the late Pliocene and Quaternary

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The occurrence of Cenozoic silicoflagellates at three Ocean Drilling Program (ODP) Holes (660A, 662A, and 667A) was investigated to determine biostratigraphic and relative paleotemperature relations in the tropical Atlantic Ocean. This report presents the data obtained from a study of 37 samples and some preliminary comments on the data. The age of the single sparse assemblage at Hole 660A is late middle Eocene or late Eocene (Dictyocha hexacantha Zone); the sparse to common assemblages of Hole 667A are Oligocene and early Miocene and the common to abundant assemblages of Hole 662A are early Pliocene to Quaternary. Dissolution thinning of silicoflagellates is noted in most samples, even in Hole 662A, which is under the present productive Benguela Current.