613 resultados para RADIALIS(RAD)


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Radiolarians are very rare in all Leg 90 sites. They are relatively more frequent only in Neogene sediments from Sites 586 and 594, and in Eocene sediments at Site 592. In this chapter radiolarian abundances are recorded as comparative percentages for 92 Neogene morphotypes at Site 586B. Relative abundances only are estimated at Sites 592 and 594, where preservation is poor to moderate. A tentative correlation of radiolarian events at Hole 586B and Site 594 shows that only a few species can be found in both tropical and subantarctic areas. New evolutionary lineages are proposed. 1. Middle Miocene eucyrtids like Eucyrtidium teuscheri group evolved into a widespread species (E. teuscheri teuscheri) ranging from middle Miocene to Holocene and a temperate species (E. teuscheri orthoporus) ranging from middle Miocene to early Pleistocene. 2. Phormostichoartus pitomorphus appears to be a temperate descendant of the cosmopolitan P. fistula and disappears in early Pleistocene time. 3. The discovery of Lamprocyrtis daniellae n.sp. calls into question the lineage L. heteroporos -> L. nigriniae. 4. The evolution of Lamprocyclas maritalis from an ancestor group (L. aff. maritalis) is located in the early part of the Pterocanium prismatium Zone.

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Leg 190 was the first of a two-leg program across the Nankai accretionary prism and Trough, offshore Japan, aiming to evaluate existing models for prism evolution and to constrain syntectonic sedimentation, deformation styles, mechanical properties, and prism hydrology (Moore, Taira, Klaus, et al., 2001; Moore et al., 2001). More than 400 volcanic ash and siliceous claystone (altered ash) layers were penetrated and sampled during drilling of the six sites from two transects across the accretionary prism (Sites 1173-1178). In sites from the subducting Shikoku Basin (Sites 1173 and 1177) and in the trench axis (Site 1174), recognition of ash layers and diagenetically altered ashes was initially important in defining major lithostratigraphic units. However, it is clear that understanding the diagenesis of the volcanic ashes has considerable implications for prism evolution, mechanical properties, prism hydrology, geochemistry, and fluid flow in the accretionary prism and associated subducting sediments (cf. Masuda et al., 1996, doi 10.1346/CCMN.1996.0440402). Particle size, chemical composition, temperature, depth of burial, and time are all thought to be factors that may affect volcanic ash diagenesis and preservation (Kuramoto et al., 1992, doi:10.2973/odp.proc.sr.127128-2.235.1992; Underwood et al., 1993, doi:10.2973/odp.proc.sr.131.137.1993). The overall aim of this research is to evaluate factors influencing volcanic ash diagenesis in the Nankai Trough area. This data report presents just the results of the sedimentological and petrographic analysis of the volcanic ashes and siliceous claystones from Sites 1173, 1174, and 1177. It is anticipated that when the results of additional geochemical analysis of these lithologies is available a more meaningful evaluation of factors influencing volcanic ash alteration will be possible.

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Site 1237 is located on Nazca Ridge ~140 km off the coast of Peru and thus within the offshore region of the Peru-Chile Current. A total of 83 samples were used to provide an initial radiolarian biostratigraphic framework for Site 1237; radiolarians are present to Sample 202-1237B-19H-2, 58-60 cm (186.45 meters composite depth [mcd]) and are of good to fair abundance and preservation. Site 1237 is influenced by both subtropical and northward-transported southern latitude waters, has 55 ash layers within the uppermost 166 m, and has minimal to gross reworking. Shipboard paleomagnetic results showed that the upper 200 m spanned the last 12 m.y., and in the upper 100 mcd, the paleomagnetic inclination pattern could be directly correlated to the geomagnetic polarity timescale (GPTS). Tropical biostratigraphy was used to establish the zonal boundaries for Site 1237, and the paleomagnetic and radiolarian stratigraphy were well correlated.

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Early to middle Miocene radiolarian assemblages were examined at three sites (747, 748, and 751) that were cored during Ocean Drilling Program Leg 120 south of the present polar frontal zone on the Kerguelen Plateau (Indian sector of the Southern Ocean). The radiolarian biostratigraphic study relies on a radiolarian zonation recently developed on Leg 113 materials in the Atlantic sector of the Southern Ocean, which is correlated with the geomagnetic time scale. New radiolarian biostratigraphic data also considering the established geomagnetic polarity record were used to improve and emend the age calibration of some lower Miocene radiolarian zones and a redefined middle Miocene radiolarian zonation is proposed. Based on these results, a revised age assignment of the lower Miocene sections drilled at Leg 113 Sites 689 and 690 is proposed.

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Indicators of surface-water productivity and bottom-water oxygenation have been studied for the age interval from the latest Pleistocene to the Holocene at three holes (679D, 680B, and 68IB) located in the center and at the edges of an upwelling cell at approximately 11°S on the Peruvian continental margin. Upwelling activity was maximal at this latitude during d18O Stages 1 (lower part), 3, the upper part of 5, the lower part of 6, and 7, as documented by high diatom abundance. During these time intervals, the bottom water was poorly oxygenated, as documented by low diversity benthic foraminiferal assemblages that are dominated by B. seminuda s.l. Both surface- and bottom-water-circulation patterns appear to have changed rapidly over short time intervals. Due to changes in surface circulation, the intensity of upwelling decreased, thereby decreasing the concentration of nutrients, and reducing the supply of organic matter to the bottom. Radiolarians became more abundant in the surface waters, and the bottom-water environment was less depleted in oxygen, allowing for the establishment of more diverse benthic foraminiferal assemblages. Surface-water productivity was probably minimal during the early part of d18O Stages 5 and 9, as indicated by the increased abundance of planktonic foraminifers and pteropods and their subsequent preservation.

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Radiolarians are sporadic in sediments collected in the Sulu Sea during ODP Leg 124. Due to the generally poor preservation and low abundance of radiolarians in Sulu Sea sediments, no biostratigraphic datums are well defined, although three radiolarian zones are identified. Most samples containing radiolarians are pelagic or hemipelagic clays with varying proportions of volcanic ash. Detailed analysis of Sulu Sea radiolarians was limited to Miocene successions. Pliocene and Quaternary occurrences of radiolarians were noted but have not been zoned. The late middle Miocene of Sites 769 and 771 is represented by an assemblage of radiolarians (Diartus petterssoni Zone) that is entirely replaced by massive pyrite. This type of preservation develops only under anoxic conditions. The development of widespread anoxia in Sulu Sea waters in the late middle Miocene was probably the result of hydrologic isolation of basin waters, and may be associated with eustatic sea level fall over the silled basin. Upper lower Miocene pelagic and hemipelagic sediments that overlie pyroclastics and basalt flows in the Sulu Sea sites contain moderately to very poorly preserved radiolarians of the Calocycletta costata Zone. A thin unit of marine claystone was recovered from between the thick pyroclastics and basement rocks at Site 768. Radiolarians present in these claystones are rare and very poorly preserved. This radiolarian assemblage probably represents the C. costata Zone, although very poor preservation and low abundance make this interpretation equivocal. The radiolarian zones identified constrain the age of basin formation to late early Miocene or earlier.

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A 100-m-thick Paleocene sequence of mainly pelagic sediments at ODP Site 1121, on the eastern flanks of the Campbell Plateau, contains few to common radiolarians of relatively low diversity in the lower 40 m (Early to early Late Paleocene) and abundant, diverse radiolarian assemblages in the upper 60 m (mid-Late Paleocene). The 150 taxa recorded from the entire Paleocene interval are thought to under-represent the actual species diversity by at least one half as many morphotypes have not been differentiated below the level of genus. Assemblages in the lower 40 m are similar to those described from onland New Zealand and DSDP Site 208 (northern Lord Howe Rise); they are correlated with South Pacific radiolarian zones RP4 and RP5. Assemblages in the upper 60 m differ from other known Late Paleocene assemblages in the great abundance of plagiacanthids and cycladophorids. Similarities are noted with later Cenozoic cool-water assemblages. This upper interval is correlated with South Pacific zone RP6, as revised herein, based on comparison with faunas from Site 208 and Marlborough, New Zealand. The interval is also correlated with the upper part of North Atlantic zone RP6 (RP6b-c) based on the presence of Aspis velutochlamydosaurus, Plectodiscus circularis and Pterocodon poculum. Other species, such as Buryella tetradica and Buryella pentadica, are valuable for local correlation but exhibit considerable diachroneity between the Pacific, Indian and Atlantic Oceans. An age model for the Paleocene interval at Site 1121, based on well-constrained nannofossil and radiolarian datums, indicates that the rate of compacted sediment accumulation doubles from 15 to 30 mm/ka at the RP5/RP6 zonal boundary. In large part this is due to a sudden and pronounced increase in accumulation rates for all siliceous fossils; radiolarians and larger diatoms increase from <100 to >10 000 specimens/cm2/ka. This apparent increase in biosiliceous productivity is age-equivalent to a mid-Paleocene cooling event (57-59 Ma) identified from global stable isotope records that is associated with the heaviest delta13C values for the entire Cenozoic.

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We propose a new biostratigraphic scheme comprising the Eucyrtidium spinosum, Eucyrtidium antiquum (new), Lychnocanoma conica (emended), Clinorhabdus robusta (emended) and Stylosphaera radiosa (emended) Zones, in ascending order, in Eocene to Oligocene sediments drilled on Maud Rise in Southern Atlantic Ocean (Site 689, Ocean Drilling Program Leg 113). The bases of these zones are defined by the lowermost occurrences of E. spinosum, E. antiquum, L. conica, C. robusta and the uppermost occurrence of Axoprunum irregularis (?), respectively. From correlation to the magnetostratigraphic data, the E. spinosum, E. antiquum, L. conica, C. robusta and S. radiosa Zones are assigned to the late middle Eocene through late Eocene (Subchrons C17n2 to C13r), earliest Oligocene (C13n to C11n), late early Oligocene (C11n to C10n2), early late Oligocene (C10n1 to C8r) and latest Oligocene (C8r to C7An), respectively. The four boundary datum levels and supplementary datum levels such as the lowermost occurrences of A. irregularis (?), Dicolocapsa microcephala and Lithomelissa challengerae may be recognized in other ODP sites in the Southern Ocean. The first occurrence of E. antiquum approximates the Eocene-Oligocene boundary in Southern Ocean but the last occurrences of many species such as Periphaena decora, D. microcephala and the Lithomelissa sphaerocephalis group are commonly diachronous between high latitude sites. Two new species, Theocyrtis (?) triapenna and Spirocyrtis parvaturris, are described.

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Radiolarians were recovered from three of the five holes investigated during Leg 125. Relative abundances are estimated at Holes 782A and 784A, where preservation is poor to good. Rare, poorly preserved radiolarians are present in Hole 786A. Seven radiolarian zones are recognized in the latest early- middle Miocene to early Pleistocene of Holes 782A and 784A. These zones are approximately correlated to the zones of Sanfilippo and others published in 1985.

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Foraminiferal assemblages in sediments from Hole 543A suggest that toward the end of the Cretaceous there was an oscillating carbonate compensation depth (CCD) in the western Central Atlantic. Changing assemblages of siliceous agglutinated and calcareous foraminifers reflect the changing depositional environment, from a ridge crest environment during Campanian time to a deep abyssal environment during Maestrichtian time.

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The Bounty Trough, east of New Zealand, lies along the southeastern edge of the present-day Subtropical Front (STF), and is a major conduit via the Bounty Channel, for terrigenous sediment supply from the uplifted Southern Alps to the abyssal Bounty Fan. Census data on 65 benthic foraminiferal faunas (>63 µm) from upper bathyal (ODP 1119), lower bathyal (DSDP 594) and abyssal (ODP 1122) sequences, test and refine existing models for the paleoceanographic and sedimentary history of the trough through the last 150 ka (marine isotope stages, MIS 6-1). Cluster analysis allows recognition of six species groups, whose distribution patterns coincide with bathymetry, the climate cycles and displaced turbidite beds. Detrended canonical correspondence analysis and comparisons with modern faunal patterns suggest that the groups are most strongly influenced by food supply (organic carbon flux), and to a lesser extent by bottom water oxygen and factors relating to sediment type. Major faunal changes at upper bathyal depths (1119) probably resulted from cycles of counter-intuitive seaward-landward migrations of the Southland Front (SF) (north-south sector of the STF). Benthic foraminiferal changes suggest that lower nutrient, cool Subantarctic Surface Water (SAW) was overhead in warm intervals, and higher nutrient-bearing, warm neritic Subtropical Surface Water (STW) was overhead in cold intervals. At lower bathyal depths (594), foraminiferal changes indicate increased glacial productivity and lowered bottom oxygen, attributed to increased upwelling and inflow of cold, nutrient-rich, Antarctic Intermediate Water (AAIW) and shallowing of the oxygen-minimum zone (upper Circum Polar Deep Water, CPDW). The observed cyclical benthic foraminiferal changes are not a result of associations migrating up and down the slope, as glacial faunas (dominated by Globocassidulina canalisuturata and Eilohedra levicula at upper and lower bathyal depths, respectively) are markedly different from those currently living in the Bounty Trough. On the abyssal Bounty Fan (1122), faunal changes correlate most strongly with grain size, and are attributed to varying amounts of mixing of displaced and in-situ faunas. Most of the displaced foraminifera in turbiditic sand beds are sourced from mid-outer shelf depths at the head of the Bounty Channel. Turbidity currents were more prevalent during, but not restricted to, glacial intervals.

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Well preserved middle Miocene to Recent radiolarians were recovered from several sites in the Weddell Sea by ODP (Ocean Drilling Program) Leg 113. Low rates of sedimentation, hiatuses, and poor core recovery in some sites are offset by the nearly complete recovery of a late middle Miocene to late Pliocene section at Site 689 on the Maud Rise. Although a hiatus within the latest Miocene exists, this site still provides an excellent reference section for Antarctic biostratigraphy. A detailed radiolarian stratigraphy for the middle Miocene to late Pliocene of Site 689 is given, together with supplemental stratigraphic data from ODP Leg 113 Sites 690, 693, 695, 696, and 697. A refined Antarctic zonation for the middle Miocene to Recent is presented, based on the previous zonations of Hays (1965), Chen (1975), Weaver (1976b), and Keany (1979). The late Miocene radiolarian Acrosphaera australis n. sp. is described and used to define the A. australis zone, ranging from the first appearance of the nominate species to the last appearance of Cycladophora spongothorax (Chen) Lombari and Lazarus 1988. The species Botryopera deflandrei Petrushevskaya 1975 is transferred to Antarctissa deflandrei (Petrushevskaya) n. comb.

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The Pliocene-Holocene sediments recovered on ODP Leg 114 from Holes 699A, 701C, and 704B are the subject of a detailed investigation to interpret changes in the Oceanographic environment of the South Atlantic in the vicinity of the Polar Front Zone (PFZ). The cores sample sediments at shallow (Hole 704B, 2532 m), intermediate (Hole 699A, 3716 m), and basinal (Hole 701C, 4647 m) depths. Sites 699 and 704 come under the influence of the Antarctic Circumpolar Current (ACC) and Circumpolar Deep Water. It is possible that the upper reaches of Antarctic Bottom Water (AABW) may also affect Hole 699A. Site 701 is influenced by AABW. Closely spaced samples were analyzed for grain-size distribution, sand fraction components, biosiliceous microfossils, organic carbon, and water content. PFZ migrations are traced using changes in bulk sedimentaccumulation rates and the abundance of the diatoms Actiniscus ssp. and Genus et species indet. 1 Fenner (1991), as well as changes in sediment grain size and composition. Diatomaceous sediments of Gilbert age in Hole 699A indicate that the PFZ was positioned over this site, but during the Gauss it migrated north, bringing in less productive Antarctic Surface Water. All cores document a very gradual southerly movement of the PFZ throughout the Matuyama (with some sharp fluctuations of the northen PFZ border over Site 704 between 1.45 and 1.83 m.y.). This regressive shift culminated in the late Matuyama. The latest Matuyama to earliest Brunhes record in Hole 699A has been removed by a hiatus lasting from 1.0 to 0.6 m.y., which was probably caused by intensification of the deep-reaching ACC. The corresponding interval in Hole 704B, the shallowest core, contains evidence of winnowing. Sharp fluctuations of large amplitude and high frequency in the lithology of the sediments from Hole 704B in the eastern South Atlantic, starting at about 0.75 m.y. and characterizing the whole Brunhes Epoch, record the rapid movement of the northern border of the PFZ over the site. These reflect strong glacial/interglacial alternations in climate. To a lesser extent, lithologic fluctuations in Hole 701C reflect the same phenomenon, whereas in Hole 699A the lithology does not vary as dramatically.