520 resultados para silicon chemistry
Resumo:
The Sahara Desert is the largest source of mineral dust in the world. Emissions of African dust increased sharply in the early 1970s, a change that has been attributed mainly to drought in the Sahara/Sahel region caused by changes in the global distribution of sea surface temperature. The human contribution to land degradation and dust mobilization in this region remains poorly understood, owing to the paucity of data that would allow the identification of long-term trends in desertification. Direct measurements of airborne African dust concentrations only became available in the mid-1960s from a station on Barbados and subsequently from satellite imagery since the late 1970s: they do not cover the onset of commercial agriculture in the Sahel region ~170 years ago. Here we construct a 3,200-year record of dust deposition off northwest Africa by investigating the chemistry and grain-size distribution of terrigenous sediments deposited at a marine site located directly under the West African dust plume. With the help of our dust record and a proxy record for West African precipitation we find that, on the century scale, dust deposition is related to precipitation in tropical West Africa until the seventeenth century. At the beginning of the nineteenth century, a sharp increase in dust deposition parallels the advent of commercial agriculture in the Sahel region. Our findings suggest that human-induced dust emissions from the Sahel region have contributed to the atmospheric dust load for about 200 years.
Resumo:
Pore-water samples were recovered at five sites from ODP Leg 114 in the subantarctic South Atlantic Ocean and analyzed for pH, alkalinity, chloride, sulfate, fluoride, silica, magnesium, calcium, strontium, potassium, lithium, and barium. At sites in the East Georgia Basin and on the Islas Orcadas Rise, Ca increases and Mg decreases linearly downhole with a DeltaMg/DeltaCa ratio reflecting conservative diffusive exchange and basalt basement reactions. At sites on the west flank of the Mid-Atlantic Ridge and on the Meteor Rise, Ca gradients are nonlinear, and nonconservative DeltaMg/DeltaCa ratios reflect alteration reactions of abundant silicic volcanic ash in the sediment. K decreases linearly downhole at all sites, reflecting uptake by basement and the absence of significant sediment-hosted reactions. SO4 decreases and alkalinity increases downhole are due to a slight sulfate reduction at all sites except at Site 701. Sr increases downhole at all sites except Site 701, with DeltaSr/DeltaCa ratios reflecting diffusive exchange with basement. At Site 704 on the Meteor Rise, there is intense Sr production during carbonate recrystallization in the upper 200 mbsf. Below 200 mbsf at Site 704, the ion concentration product of SrSO4 is constant, suggesting Sr control by celestite solubility. Li and F concentrations display complex behavior related to sedimentary reactions, probably calcite recrystallization (Li uptake and F release).
Resumo:
Distributions of pore water O2, NO-2, NO-3, NH+4, Si(OH)4, PO[3-]4, Mn[2+], F-, and T.A. were determined at 15 stations in the eastern equatorial Atlantic. While overall profile characteristics are consistent with previous models of organic matter diagenesis, profile shapes suggest that a deep reaction layer, rich in organic C, is also present at many sites. While it is unlikely that the oxidation of organic C in this layer has had a major effect on the ocean C cycle, pore water profile shapes are significantly altered. Despite exposure to seawater SO[2-]4 concentrations for > 1000 years, decomposition of the organic matter in the layer appears to be restricted to oxic and suboxic processes. These results suggest major differences in organic carbon decomposition and preservation under oxic/suboxic and anoxic conditions. Present-day benthic fluxes are largest adjacent to the eastern boundary coastal upwelling region and similar in magnitude to values reported for the eastern Pacific. Preliminary estimates suggest that the benthic respiration in the eastern 1/3 of the North Atlantic south of 20°N may alone account for >20% of the total deep North Atlantic respiration. Combining these results with estimates of organic C burial and deep water-column decomposition suggests that this region is a major location of organic C input into the deep sea.
Resumo:
Pore water was collected from sediment cores from Holes 1202A and 1202D in the southern Okinawa Trough during Ocean Drilling Program (ODP) Leg 195. Because drilling at this site was completed only a few hours out of port during the end of the leg, whole rounds of sediment core 5 or 10 cm long were sealed and stored at ~3°C until pore water could be extracted from them during Leg 196, using a titanium squeezer designed by Manheim and Sayles (1974) and standard handling techniques (Shipboard Scientific Party, 2002, doi:10.2973/odp.proc.ir.195.103.2002).
Resumo:
Thick pumice deposits were found in the cored sequences of forearc, arc, and backarc sites of Leg 126 in the Izu-Bonin Arc. These deposits, composed of fragmental rhyolite pumice with the chemical composition of low-alkali tholeiites, are products of arc volcanism. Pumice deposits constitute more than half of the thickness of the sediment fill of the Sumisu Rift, a backarc rift of the Izu-Bonin Arc. They comprise five thick pumiceous beds separated by thin hemipelagic units; as such, they record four major episodes or pulses of explosive, rhyolitic volcanism during the last 0.15 Ma, separated by quiescent intervals that each lasted about 30-60 k.y. The thick pumiceous beds were deposited in the rift mainly by sediment gravity flows during and immediately after the eruption of arc volcanos, which were probably submarine. Initiation of rifting was also preceded in the Pliocene by submarine rhyolitic volcanism, as seen in samples from the top of the eastern rift flank. Thick pumice beds correlative with those in the backarc also occur in the forearc basin to the east.