526 resultados para Holymenia clavigera
Resumo:
We provide high-resolution sea surface temperature (SST) and paleoproductivity data focusing on Termination 1. We describe a new method for estimating SSTs based on multivariate statistical analyses performed on modern coccolithophore census data, and we present the first downcore reconstructions derived from coccolithophore assemblages at Ocean Drilling Project (ODP) Site 1233 located offshore Chile. We compare our coccolithophore SST record to alkenone-based SSTs as well as SST reconstructions based on dinoflagellates and radiolaria. All reconstructions generally show a remarkable concordance. As in the alkenone SST record, the Last Glacial Maximum (LGM, 19-23 kyr B.P.) is not clearly defined in our SST reconstruction. After the onset of deglaciation, three major warming steps are recorded: from 18.6 to 18 kyr B.P. (~2.6°C), from 15.7 to 15.3 kyr B.P. (~2.5°C), and from 13 to 11.4 kyr B.P. (~3.4°C). Consistent with the other records from Site 1233 and Antarctic ice core records, we observed a clear Holocene Climatic Optimum (HCO) from ~8-12 kyr B.P. Combining the SST reconstruction with coccolith absolute abundances and accumulation rates, we show that colder temperatures during the LGM are linked to higher coccolithophore productivity offshore Chile and warmer SSTs during the HCO to lower coccolithophore productivity, with indications of weak coastal upwelling. We interpret our data in terms of latitudinal displacements of the Southern Westerlies and the northern margin of the Antarctic Circumpolar Current system over the deglaciation and the Holocene.
Resumo:
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.
Resumo:
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.
Resumo:
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
Resumo:
As a continuation of the Japan Trench transect commenced by DSDP Leg 56, 10 holes were drilled and 273 cores were recovered while occupying Sites 438, 439, 440, and 441 during Leg 57. At Sites 438 and 439, near the top of the trench inner wall, a principal biostratigraphic objective was to establish a Neogene reference section overlying a pronounced acoustic basement thought to represent continental crust extending outward to this slope environment. At Sites 440 and 441, prime objectives were to distinguish, if present, admixtures of accreted oceanic and non-accreted slope materials, and to recognize repeated or missing sections resulting from the accretionary process. This report summarizes the nannofossil biostratigraphy of the upper lower Miocene to Pleistocene sequences of Leg 57 cores. Insufficient occurrences in the lowermost Miocene, presumed upper Oligocene, and upper Cretaceous sequences at Sites 438 and 439 precluded age determinations for these intervals based on nannoliths. All but a few samples from Site 441 were barren, and in general Leg 57 nannofossil assemblages were too modified by dissolution and diagenesis to permit meaningful paleoclimatologic or paleobiogeographic conclusions to be drawn.
Resumo:
During Leg 43, six holes (Sites 382-387) were drilled in the western part of the North Atlantic Ocean; locations of sites are shown in Figure 1. Lower Cretaceous to Quaternary calcareous nannofossils were found in 127 of 189 cores recovered during the leg. The ages and zonal assignments of these fossiliferous cores based upon light-microscopical observation are given in Table 1. An almost continuous succession of nannofossil assemblages of the lower Maestrichtian to upper Paleocene is present at Site 384. A detailed investigation was conducted on samples at this site, and the evolution of approximately 50 species is documented through almost the entire Paleocene epoch.
Resumo:
Samples were examined for diatoms from 22 holes at 11 sites cored by ODP Leg 119 on the Kerguelen Plateau and in Prydz Bay, East Antarctica. Diatoms were observed in Oligocene through Holocene sediments recovered from the Kerguelen Plateau. The diatom flora from the Kerguelen Plateau is characterized by species such as Azpeitia oligocenica, Rocella gelida, Rocella vigilans, and Synedra jouseana in the Oligocene and Crucidenticula nicobarica, Denticulopsis hustedtii, Nitzschia miocenica, and Thalassiosira miocenica in the Miocene. This somewhat cosmopolitan assemblage gives way to a Pliocene and Holocene assemblage characterized by species such as Nitzschia kerguelensis, Thalassiosira inura, and Thalassiosira torokina, which are endemic to the Southern Ocean region. Samples examined from Prydz Bay are generally devoid of diatoms. The exception is Site 739, where diatoms occur sporadically in lower Oligocene and upper Miocene through Quaternary sediments. The Leg 119 diatom biostratigraphic results allow the development of a stratigraphic framework for the Indian sector of the Southern Ocean. This diatom zonation integrates diatom zonations developed previously for other sectors of the Southern Ocean. The zonation proposed here is based on biostratigraphic events of both geographically widespread and endemic species calibrated to the paleomagnetic stratigraphy. As such, this zonation has application throughout the Southern Ocean and allows correlation from the southern high latitudes to the low latitudes.