965 resultados para Sedimentary sands
Resumo:
An extensive radiograph study of 24 undisturbed, up to 206-cm long box and gravity cores from the western part of the Strait of Otranto revealed a great variety of primary bedding structures and secondary burrowing features. The regional distribution of the sediments according to their structural, textural, and compositional properties reflects the major morphologic subdivisions of the strait into shelf, slope, and trough bottom (e.g., the bottom of the northern end of the Corfu-Kephallinia Trough, which extends from the northeastern Ionian Sea into the Strait of Otranto): (1) The Apulian shelf (0 to -170m) is only partly covered by very poorly sorted, muddy sands without layering. These relict(?) sands are rich in organic carbonate debris and contain glauconite and reworked (?Pleistocene) ooids. (2) The slope sediments (-170 to -1,000 m) are poorly sorted, sandy muds with a high degree of burrowing. One core (OT 5) is laminated and shows slump structures. An origin of these slumped sediment masses from older deposits higher on the slope was inferred from their abnormal compaction, color, texture, organic content, and mineral composition. (3) Cores from the northern end of the Corfu-Kephallinia Trough (-980 to -1,060 m) display a few graded sand layers, 2-5 cm (maximum 30 cm) thick with parallel and ripple-cross-laminations, deposited by oceanic bottom or small-scale turbidity currents. They are intercalated with homogeneous lutite. (4) Hemipelagic sediments prevail in the more southerly part of the Corfu-Kephallinia Trough and on the "Apulian-Ionian Ridge", the southern submarine extension of the Apulian Peninsula. Below a core depth of 160 cm, these cores have a laminated ("varved") zone, representing an Early Holocene (Boreal-Atlanticum) "stagnation layer" (14C age approximately 9,000 years). The terrigenous components of the surface sediments as well as those of the deeper sand layers can be derived from the Apulian shelf and the Italian mainland (Cretaceous Apulian Plateau and Gargano Mountains, southern Apennines, volcanic province of the Monte Vulture). Indicated by the heavy mineral glaucophane, a minor proportion of the sedimentary material is probably of Alpine origin. If this portion is considered to be first-cycle clastic material it reaches the Strait of Otranto after a longitudinal transport of 700 km via the Adriatic Sea. The lack of phyllosilicates in the coarse- to medium-grained shelf samples might be explained by the activity of the "Apulian Current" (surface velocities up to 4 knots) which in the past possibly has affected the bottom almost down to depths of the shelf edge. The percentage of planktonic organisms, and also the plankton: benthos ratio in the sediments is a useful indicator for bathymetry (depth zonation).
Resumo:
Mineral assemblages of DSDP Holes 436 and 438A and the upper section of Hole 439 (871.5-911.0 m sub-bottom) resemble each other and are composed of montmorillonite (probably a small portion of montmorillonite/illite mixed-layer clays), illite, chlorite, kaolinite, quartz, plagioclase, hornblende, calcite, dolomite, siderite, gypsum, pyrite, and halite. In the middle section of Hole 439 (933.5-1041.0 m), clinoptilolite is also found. In the lower section of Hole 439 (1077.5-1150.0 m), montmorillonite is not confirmed, and clinoptilolite and mixed-layer illite are found. These assemblages, which also contain detrital kaolinite, are generally found in sediments from brackish-water environments. At Site 439, more than 1000 meters of sediment might have been removed by erosion at the base.
Eocene sedimentary calcium carbonate contents and stable isotope composition of benthic foraminifera
Resumo:
'Hyperthermals' are intervals of rapid, pronounced global warming known from six episodes within the Palaeocene and Eocene epochs (~65-34 million years (Myr) ago) (Zachos et al., 2005, doi:10.1126/science.1109004; 2008, doi:10.1038/nature06588; Roehl et al., 2007, doi:10.1029/2007GC001784; Thomas et al., 2000; Cramer et al., 2003, doi:10.1029/2003PA000909; Lourens et al., 2005, doi:10.1038/nature03814; Petrizzo, 2005, doi:10.2973/odp.proc.sr.198.102.2005; Sexton et al., 2006, doi:10.1029/2005PA001253; Westerhold et al., 2007, doi:10.1029/2006PA001322; Edgar et al., 2007, doi:10.1038/nature06053; Nicolo et al., 2007, doi:10.1130/G23648A.1; Quillévéré et al., 2008, doi:10.1016/j.epsl.2007.10.040; Stap et al., 2010, doi:10.1130/G30777.1). The most extreme hyperthermal was the 170 thousand year (kyr) interval (Roehl et al., 2007) of 5-7 °C global warming (Zachos et al., 2008) during the Palaeocene-Eocene Thermal Maximum (PETM, 56 Myr ago). The PETM is widely attributed to massive release of greenhouse gases from buried sedimentary carbon reservoirs (Zachos et al., 2005; 2008; Lourenbs et al., 2005; Nicolo et al., 2007; Dickens et al., 1995, doi:10.1029/95PA02087; Dickens, 2000; 2003, doi:10.1016/S0012-821X(03)00325-X; Panchuk et al., 2008, doi:10.1130/G24474A.1) and other, comparatively modest, hyperthermals have also been linked to the release of sedimentary carbon (Zachos et al., 2008, Lourens et al., 2005; Nicolo et al., 2007; Dickens, 2003; Panchuk et al., 2003). Here we show, using new 2.4-Myr-long Eocene deep ocean records, that the comparatively modest hyperthermals are much more numerous than previously documented, paced by the eccentricity of Earth's orbit and have shorter durations (~40 kyr) and more rapid recovery phases than the PETM. These findings point to the operation of fundamentally different forcing and feedback mechanisms than for the PETM, involving redistribution of carbon among Earth's readily exchangeable surface reservoirs rather than carbon exhumation from, and subsequent burial back into, the sedimentary reservoir. Specifically, we interpret our records to indicate repeated, large-scale releases of dissolved organic carbon (at least 1,600 gigatonnes) from the ocean by ventilation (strengthened oxidation) of the ocean interior. The rapid recovery of the carbon cycle following each Eocene hyperthermal strongly suggests that carbon was resequestered by the ocean, rather than the much slower process of silicate rock weathering proposed for the PETM (Zachos et al., 2005; 2003). Our findings suggest that these pronounced climate warming events were driven not by repeated releases of carbon from buried sedimentary sources (Zachos et al., 2008, Lourens et al., 2005; Nicolo et al., 2007; Dickens, 2003; Panchuk et al., 2003) but, rather, by patterns of surficial carbon redistribution familiar from younger intervals of Earth history.
Resumo:
Lower Oligocene to Pleistocene volcaniclastic sands and sandstones recovered around the Izu-Bonin Arc during Ocean Drilling Program Leg 126 were derived entirely from Izu-Bonin Arc volcanism. Individual grains consist of volcanic glass, pumice, scoria, basaltic or andesitic fragments, plagioclase, pyroxene, and minor olivine and hornblende. In Pliocene-Pleistocene samples plagioclase and heavy minerals in the volcaniclastic sands and sandstones are present in the following abundances: plagioclase > orthopyroxene > clinopyroxene > pigeonite > olivine. In contrast, plagioclase and heavy minerals found in Oligocene-Miocene samples occur in the following order: plagioclase > clinopyroxene > orthopyroxene > hornblende. The low concentration of Al, Ti, and Cr in calcium-rich clinopyroxenes in Oligocene to Holocene sediments suggests that the sources of the volcaniclastic detritus were nonalkalic igneous rocks. There are, however, some distinctive differences in the chemical composition of pyroxene between the Pliocene-Pleistocene and Oligocene-Miocene volcaniclastic sands and sandstones. Orthopyroxene belongs to the hypersthene-ferrohypersthene series (Fe-rich) in Pliocene-Pleistocene sediments, and the bronzitehypersthene series (Mg-rich) in Oligocene-Miocene sediments. Clinopyroxene is characterized by augite and pigeonite in Pliocene-Pleistocene sediments, and by the diopside-augite series in Oligocene-Miocene sediments. Mineral assemblages and mineral chemistry of the volcaniclastic sands and sandstones reflect those of the volcanic source rocks. Therefore, the observed changes in mineralogy record the historical change in volcanism of the Izu-Bonin Arc. The mineralogy is consistent with the geochemistry of the volcaniclastic sands and sandstones and the geochemistry of forearc volcanic rocks of the Izu-Bonin Arc since the Oligocene.
Resumo:
One hundred and twenty point counts of Oligocene to Recent sands and sandstones from DSDP sites in the Japan and Mariana intraoceanic forearc and backarc basins demonstrate that there is a clear compositional difference between the continentally influenced Japan forearc and backarc sediments, and the totally oceanic Mariana forearc and backarc sediments. Japan forearc sediments average 10 QFL%Q, 0.82 P/F, 2 Framework%Mica, 74 LmLvLst%Lv, and 19 LmLvLst%Lst. In contrast, the Mariana forearc and backarc sediments average 0 QFL%Q, 1.00 P/F, 0 Framework%Mica, 98 LmLvLst%Lv, and 1 LmLvLst%Lst. Sediment compositions in the Japan region are variable. The Honshu forearc sediments average 5 QFL%Q, 0.94 P/F, 1 Framework%Mica, 82 LmLvLst%Lv, and 15 LmLvLst%Lst. The Yamato Basin sediments (DSDP Site 299) average 13 QFL%Q, 0.70 P/F, 3 Framework%Mica, 78 LmLvLst%Lv, and 14 LmLvLst%Lst. The Japan Basin sediments (DSDP Site 301) average 24 QFL%Q, 0.54 P/F, 9 Framework%Mica, 58 LmLvLst%Lv, and 21 LmLvLst%Lst. P/F and Framework%Mica are higher in the Yamato Basin sediments than in the forearc sediments due to an increase in modal potassium content of volcanic rocks from east to west, on the island of Honshu. Site 301 possesses a higher QFL%Q and LmLvLst%Lst, and lower LmLvLst%Lv than Site 299 because it receives sediment from the Asian mainland as well as the island of Honshu. DSDP Site 293 sediments, in the Mariana region, average 0.97 P/F, 1 Framework%Mica, 13 LmLvLst%Lm and 83 LmLvLst%Lv, due to their proximity to the island of Luzon. The remaining Mariana forearc and backarc sediments show a uniform composition.
Resumo:
Selective degradation of organic matter in sediments is important for reconstructing past environments and understanding the carbon cycle. Here, we report on compositional changes between and within lipid classes and kerogen types (represented by palynomorph groups) in relation to the organic matter flux to the sea floor and oxidation state of the sediments since the early Holocene for central Eastern Mediterranean site ABC26. This includes the initially oxic but nowadays anoxic presapropelic interval, the still unoxidised lower part of the organic rich S1 sapropel, its postdepositionally oxidised and nowadays organic-poor upper part as well as the overlying postsapropelic sediments which have always been oxic. A general ~ 2.3 times increase in terrestrial and marine input during sapropel formation is estimated on the basis of the total organic carbon (TOC), pollen, spore, dinoflagellate cyst, n-alkane, n-alkanol and n-alkanoic acid concentration changes in the unoxidised part of the sapropel. The long-chain alkenones, 1,15 diols and keto-ols, loliolides and sterols indicate that some plankton groups, notably dinoflagellates, may have increased much more. Apart from the terrestrial and surface water contributions to the sedimentary organic matter, anomalous distributions and preservation of some C23-C27 alkanes, alkanols and alkanoic acids have been observed, which are interpreted as a contribution by organisms living in situ. Comparison of the unoxidised S1 sapropel with the overlying oxidised sapropel and the organic matter concentration profiles in the oxidised postsapropelic sediments demonstrates strong and highly selective aerobic degradation of lipids and palynomorphs. There seems to be a fundamental difference in degradation kinetics between lipids and pollen which may be possibly related with the absence of sorptive preservation as a protective mechanism for palynomorph degradation. The n-alkanes, Impagidinium, and Nematosphaeropsis are clearly more resistant than TOC. The n-alkanols and n-carboxylic acids are about equally resistant whereas the pollen, all other dinoflagellate cysts and other lipids appear to degrade considerably faster, which questions the practice of normalising to TOC without taking diagenesis into account. Selective degradation also modifies the relative distributions within lipid classes, whereby the longer-chain alkanes, alcohols and fatty acids disappear faster than their shorter-chain equivalents. Accordingly, interpretation of lipid and palynomorph assemblages in terms of pre- or syndepositional environmental change should be done carefully when proper knowledge of the postdepositional preservation history is absent. Two lipid-based preservation proxies are tested the diol-keto-ol oxidation index based on the 1,15C30 diol and keto-ols (DOXI) and the alcohol preservation index (API) whereby the former seems to be the most promising.