共查询到20条相似文献，搜索用时 203 毫秒
1.
Atmospheric precipitation samples were collected in the Bohemian Karst (30 km SW from Prague, Czech Republic) at six localities in the vicinity of the limestone-quarry Čertovy schody during years 1996–2003. Samples were analyzed for major components (Na +, K +, Mg 2+, Ca 2+, F −, Cl −, NO 3−, HCO 3−, SO 42−) and trace metals (Cu, Mn, Fe, Zn, Pb, Be, As, Sr, Cd, Al, Cr). Deposition fluxes were calculated from more than 10 000 elemental analyses of samples collected monthly. The fluxes of monitored substances show temporal and spatial variability. The most marked attribute is the strong affection by local emission sources confirmed by the investigation of seasonal variability, temporal trend and correlation analysis. 相似文献
2.
Iron transformations in a calcium carbonate rich fresh-water sediment were studied by analyzing the relevant constituents of both interstitial water and solid matter. Analysis of interstitial water shows that the observed redox sequence NO −3/NH +4, MnO 2/Mn(II), FeOOH/Fe(II), SO 2−4/S(−II) is roughly in agreement with that predicted by the Gibbs Free Energy for the corresponding reactions. In contrast to marine sediments, these redox transitions occur in the uppermost sediments, i.e., at depths of 0–4 cm. Deeper in the sedimentary sequence, the depth profile for dissolved iron exhibits a steady non-linear increase up to 400 μmol dm−3. In this anoxic zone, according to thermodynamic predictions, iron (II)-minerals such as iron sulfide, siderite, and vivianite should precipitate while Fe(III) oxides should be completely dissolved. However, microscopic analysis showed that Fe(III) oxides were present throughout the studied sediment. Furthermore, scanning electron microscope/energy dispersive spectroscopy analysis suggests the presence of iron sulfide could be verified but not that of siderite or vivianite. These observations indicate kinetic control of iron transformations. We have investigated the importance of kinetic control of iron distribution in anoxic sediments using a diagenetic model for dissolved iron(II). A rough estimate of time scales for dissolution and precipitation rates was made by imposing limiting boundary conditions. Using the calculated rate constant, we established that more than 1000 years would be required for the complete dissolution of Fe(III) oxides, which is agreement with our observations and experimental data from the literature. Calculated precipitation rates of Fe(II) for a given mineral phase such as siderite yield a maximum value of 3 μg(FeCO3) g−1(dry sediment) yr−1. Such low rates would explain the absence of siderite and vivianite. Finally, it can be inferred from the MnT/FeT ratio in the sediments that this ratio depends on the redox conditions of the sediment-water interface at the time of deposition. Thus, this ratio can be used as “paleo-redox indicator” in lacustrine sediments. 相似文献
3.
Concretions of vivianite attaining 0.5 g occur in the upper 4 m of the bottom sediments of the Åsrum lake, Vestfold, S. Norway. The vivianite-bearing zone is of lacustrine origin. Vivianite is absent in the underlying lagunal and marine sediments. Electro-chemical and chemical data are given for the interstitial water and the clay. Solubility product of vivianite is determined. The equilibrium constant is K = 10−40 for the reaction 3 Fe++ + 2 HPO4− + 2 OH− = vivianite. The concretions grew by diffusion from a slightly supersaturated interstitial water phase. The degree of supersaturation is calculated. The stability relations of vivianite and hydroxyl apatite are discussed. 相似文献
4.
碳酸盐岩的Fe/Mn元素比值,作为一项新的地球化学指标,可以用于恢复海洋的氧化还原状态.在氧化条件下,Fe 3+和Mn 4+均不可溶,因此氧化海水中的溶解Fe和Mn的含量均很低.Fe 3+和Mn 4+在还原条件下可以被细菌还原为可溶的Fe 2+和Mn 2+,而氧化还原电位的计算表明,Mn 4+的还原要早于Fe 3+的还原,因此细菌的Mn还原过程发生在沉积物的更浅层.可溶的Fe 2+和Mn 2+向上扩散到海水中,替代碳酸盐岩晶格里的Ca 2+,因此碳酸盐岩晶格中的Fe 2+和Mn 2+的含量受控于来自沉积物孔隙水的扩散,而后者又与水岩界面的氧化还原状态相关.因此可以预测,随着海水变得逐渐缺氧,碳酸盐岩中的Fe/Mn比值会逐渐增高.为了验证这一假说,我们分析了中元古代高于庄组白云岩的Fe/Mn比值.研究发现,几乎所有的样品的Fe/Mn比值介于20～30之间,显著高于泥盆纪末期深水碳酸盐岩和浅水台地碳酸盐岩的Fe/Mn比值.高于庄组碳酸盐岩高的Fe/Mn比值一方面可能指示了中元古代低的大气氧气浓度和海洋的广泛缺氧,也可能反映了白云岩形成于缺氧的沉积物空隙水里. 相似文献
5.
Dissolution rates of single calcite crystals were determined from sample weight loss using free-drift rotating disk techniques. Experiments were performed at 25 °C in aqueous HCl solutions over the bulk solution pH range −1 to 3 and in the presence of trace concentrations of aqueous NaPO 3 and MgCl 2. These salts were chosen for this study because aqueous magnesium and phosphate are known to strongly inhibit calcite dissolution at neutral to basic pH. Reactive solutions were undersaturated with respect to possible secondary phases. Neither an inhibition or enhancement of calcite dissolution rates was observed in the presence of aqueous MgCl 2 at pH 1 and 3. The presence of trace quantities of NaPO 3, which dissociates in solution to Na + and H 2PO 4−, decreased the overall calcite dissolution rate at pH≤2. This contrasting behavior could be attributed to the different adsorption behavior of these dissolved species. As calcite surfaces are positively charged in acidic solutions, aqueous Mg 2+ may not adsorb, whereas aqueous phosphate, present as either the anion H 2PO 4− or the neutral species H 3PO 40, readily adsorbs on calcite surfaces leading to significant dissolution inhibition. 相似文献
6.
The Loire River, with one of the largest watersheds in France, has been monitored just outside the city of Orleans since 1994. Physico-chemical parameters and major and trace elements were measured between 2-day and 1-week intervals according to the river flow. The sampling site represents 34% of the total Loire watershed with 76% silicate rocks and 24% carbonate rocks. Elements are transported mainly in the dissolved phase with the ratio of total dissolved salts (TDS) to suspended matter (SM) ranging between 1.6 and 17.4. Chemical weathering of rocks and soils are thus the dominant mechanisms in the Loire waters composition. The highest TDS/SM ratios are due to dissolved anthropogenic inputs. The database shows no link between NO3− content and river flow. The Na+, K+, Mg2+, SO42−, and Cl− concentrations are seen to decrease with increasing discharge, in agreement with a mixing process involving at least two components: the first component (during low flow) is concentrated and may be related with input from the groundwater and sewage station water, the second component (during high flow) is more dilute and is in agreement with bedrock weathering and rainwater inputs. A geochemical behaviour pattern is also observed for HCO3− and Ca2+ species, their concentrations increase with increasing discharge up to 300 m3/s, after which, they decrease with increasing discharge. The Sr isotopic composition of the dissolved load is controlled by at least five components — a series of natural components represented by (a) waters draining the silicate and carbonate bedrock, (b) groundwater, and (c) rainwaters, and two kinds of anthropogenic components. The aim of this study is to describe the mixing model in order to estimate the contribution of each component. Finally, specific export rates in the upper Loire watershed were evaluated close to 12 t year−1 km−2 for the silicate rate and 47 t year−1 km−2 for the carbonate rate. 相似文献
7.
Pore water studies enable (1) the detection of diagenetic reactions actively occurring in the sediment at the time of sampling,(2)
the distinction between principal modes of solute transport, i.e., between advection (convection) and diffusion, and (3) the
assessment of mineral-solution equilibria, Pore waters are, therefore, preferred diagnostic objects in the study of diagenesis,
particularly early diagenesis.
The single most important factor for pore-fluid evolution in modern offshore basins is sedimentation rate which is closely
correlated with organtic matter content of the sediment. Organic matter represents the most reactive sediment constituent
which, through bacterial decomposition, provides some of the main solutes involved in early diagenetic mineralization reactions.
On the basis of sedimentation rate and organic matter content, it is convenient to distinguish two end-members of basins (environments)
with respect to early diagenesis: I. Low to intermediate-sedimentation rate basins with convection or diffusion-controlled
pore-water profiles and II. high-sedimentation rate basins with reaction-controlled pore-water profiles.
The first group of basins or environments, which is the subject of this paper, is typically represented by pelagic sediments.
Three principally different trends of pore-water evolution occur: 1. convection-controlled profiles with no pronounced vertical
gradients for the dissolved species; 2. diffusion-controlled profiles with vertical gradients but linear correlations between
major ions, especially Ca and Mg, and 3. profiles with gradients but no linear correlation between the major ions. The later
are transitional to the trends seen in high-sedimentation rate basins. With respect to redox-potentials, the diagenetic environments
of low-sedimentation rate basins are generally oxic to suboxic. 相似文献
8.
为了研究湿地香蒲种群对不同水深环境的生态响应规律和特征，分别于2018-06-30，2018-07-30，2018-08-29，2018-09-28进行野外采样，通过调查和室内化学分析，探讨了7个不同淹水深度下香蒲种群生长指标、水质因子和底泥因子的变化情况。结果表明：在不同淹水深度下，香蒲的生长指标差异显著，当淹水深度为50 cm时，香蒲的生长状态最优；4个采样日石佛寺水库水样大体呈弱碱性，底泥类型为中性偏酸性；随着淹水深度的增加，水样中的溶解氧（DO）、硝态氮（NO 3-）和亚硝态氮（NO 2-）质量浓度逐渐减小，总氮（TN）和氨氮（NH 4+）质量浓度增大，底泥中氨氮（NH 4+）和有机碳（SOC）质量分数总体增大，总氮（TN）、硝态氮（NO 3-）和亚硝态氮（NO 2-）质量分数逐渐减小，电导率总体逐渐降低，总磷（TP）和速效磷（AP）的质量分数基本呈波动状态。底泥和水体中氮元素的含有量对香蒲的生长影响较大。 相似文献
9.
The adsorption of phosphorus on natural diagenetic iron (Feox) and manganese (Mnox) oxyhydroxides was studied in deep and littoral zone sediments of mesotrophic Lac Saint-Charles (46°56 N, 71°23 W), using a Teflon sheet technique for collecting diagenetically produced metal oxyhydroxides. Collected metal oxide amounts were greater at the deep-water station, relative to littoral zone stations reflecting sediment and local diagenetic differences. Two-layer surface complexation modeling on iron oxyhydroxide was consistent with the measured total P/Fe molar ratios except for the upper mixed Mn–Fe oxide layer from the littoral stations, where measured phosphorus exceeded the modeled phosphorus by more than fivefold. Soluble reactive phosphorus (SRP) exchange between oxyhydroxide samples and natural lake water in the laboratory revealed a labile phosphorus pool. Phosphorus determined on the Teflon sheets from the littoral zone stations appears to be related to a distinct non-humic organic carbon pool that readily exchanges SRP, while little exchange was observed from material collected from the deep-water station. We suggest that the enhanced SRP release from littoral zone sediments is due to an organic carbon and/or metal oxide-impoverished sediment matrix, limiting microbial oxide reduction and allowing phosphorus to be rapidly recycled at the sediment–water interface, instead of being slowly incorporated into humic material. The SRP fluxes revealed in our study, which originate from the solid phase at the sediment–water interface, would be difficult to resolve using interstitial pore-water samplers and might be a quantitatively important source of inorganic phosphorus in Shield lakes. 相似文献
10.
An integrated geophysical and sedimentological investigation of the Selvage sediment-wave field has revealed that the sediment waves are formed beneath unconfined turbidity currents. The sediment waves occur on the lower continental rise and display wavelengths of up to 1 km and wave heights of up to 6 m. Wave sediments consist of interbedded turbidites and pelagic/hemipelagic marls and oozes. Nannofossil-based dating of the sediments indicates a bulk sedimentation rate of 2·4 cm 1000 years –1, and the waves are migrating upslope at a rate of 0·28 m 1000 years –1. Sediment provenance studies reveal that the turbidity currents maintaining the waves are largely sourced from volcanic islands to the south. Investigation of existing models for sediment-wave formation leads to the conclusion that the Selvage sediment waves form as giant antidunes. Simple numerical modelling reveals that turbidity currents crossing the wave field have internal Froude numbers of 0·5–1·9, which is very close to the antidune existence limits. Depositional flow velocities range from <6 to 125 cm –1. There is a rapid increase in wavelength and flow thickness in the upper 10 km of the wave field, which is unexpected, as the slope angle remains relatively constant. This anomaly is possibly linked to a topographic obstacle just upslope of the sediment waves. Flows passing over the obstacle may undergo a hydraulic jump at its boundary, leading to an increase in flow thickness. In the lower 15 km of the wave field, flow thickness decreases downslope by 60%, which is comparable with results obtained for other unconfined turbidity currents undergoing flow expansion. 相似文献
11.
Deep-sea sediments can contain relatively high concentrations of rare earth elements and yttrium (REY), with a growing interest in their exploitation as an alternative to land-based REY resources. To understand the processes that lead to enrichment of the REY in deep-sea sediments, we have undertaken a detailed geochemical study of sediments recovered from the Atlantic Ocean, on a transect along ~ 24°N that includes the deep Nares Abyssal Plain and the Canary and North America Basins.Total REY concentrations (ΣREY) range from 7.99 to 513 ppm, and total concentrations of the heavy REY (Eu - Lu) range from 0.993 to 56.3 ppm. REY concentrations are highest in slowly accumulating pelagic red clays, especially in samples that contain ferromanganese micronodules. Factor analysis reveals that hydrogenous Fe- and Mn-(oxyhydr)oxides are the primary REY carrier phase in the red clays. In situ analysis of individual micronodules confirms that they have high ΣREY (up to 3620 ppm). REY concentrations are higher in micronodules that have a hydrogenous source, characterised by higher Fe/Mn, compared to micronodules that have a diagenetic source.The ΣREY content of North Atlantic deep-sea sediments is ~ 4 times lower than in Pacific deep-sea sediments. We calculate that the area of seafloor required to extract ~ 10% of the global annual REY demand is ~ 100 km 2, assuming removal of the upper 1 m of sediment. 相似文献
12.
灌溉等人为活动会造成外源物质的输入,如硝酸盐、有机质等,从而引起浅层地下水环境发生周期性波动。为研究农业灌溉对沉积含水层中碘迁移富集过程的影响,选取代表性富碘沉积物,通过室内实验模拟了灌溉活动外源物质输入条件下,盆地地下水系统中碘迁移释放的（生物）地球化学过程。实验结果表明：厌氧条件下,外源有机质输入可促使微生物利用有机质作为电子供体,还原固相铁矿物相,进而造成搭载于铁氧化物/氢氧化物表面的碘释放,以碘离子形式在地下水中富集;而在NO 3-输入情况下,微生物会优先利用NO 3-为电子受体,至硝酸盐被全部消耗后,Fe（Ⅲ）可进一步被还原为Fe（Ⅱ）。研究结果表明,人为活动造成浅表环境外源物质的输入可直接影响浅层地下水中碘的迁移释放过程。伊利石黏土矿物吸附的铁氧化物矿物相可能为浅层环境中碘的主要搭载介质,微生物作用下,铁氧化物/氢氧化物的还原溶解是高碘地下水形成的主控因素。 相似文献
13.
Ferromanganese microcrusts were found in oxic sediments that are undisturbed between 60 and 480 cm bsf. Rhythmic alternations of muddy calcareous ooze and foraminiferal-nannofossil ooze make up the sediment sequence, which extends to 270 ka at 480 cm bsf where a hiatus of at least 1.3 Myr occurs. The bottom of the core is Pliocene. The occurrence of ferromanganese microcrusts mainly formed on foraminifera tests larger than 200 μm can be correlated with glacial stages 4, 6 and 8 and indicates enhanced metal fluxes. They do not form at the expense of carbonate material but derive their metals from the water column by hydrogenetic precipitation. Manganese was supplied as Mn 2+ mainly from the oxygen minimum zone (OMZ), where it is transported via detrital material and brought into solution by weakly reducing conditions promoted by the oxidation of organic matter. An enhanced detrital flux during glacials may also cause increased Mn availability in the OMZ during these periods. Mixing of oxygen-rich intermediate water with OMZ water during the glacial intervals caused Mn 2+ oxidation in the water column underneath the OMZ. 相似文献
14.
The Gulf of Corinth is a graben, which has undergone extension during the Late Quaternary. The subsidence rate is rapid in the currently marine part whereas uplift now affects a large part of the initially subsiding area in the North Peloponnese. In this paper, we document the rates of subsidence/uplift and extension based on new subsurface data, including seismic data and long piston coring in the deepest part of the Gulf. Continuous seismic profiling data (air gun) have shown that four (at least) major oblique prograding sequences can be traced below the northern margin of the central Gulf of Corinth. These sequences have been developed successively during low sea level stands, suggesting continuous and gradual subsidence of the northern margin by 300 m during the Late Quaternary (last 250 ka). Subsidence rates of 0.7–1.0 m kyr − 1 were calculated from the relative depth of successive topset to foreset transitions. The differential total vertical displacement between the northern and the southern margins of the Corinth graben is estimated at about 2.0–2.3 m kyr − 1. Sequence stratigraphic interpretation of seismic profiles from the basin suggests that the upper sediments (0.6 s twtt thick) in the depocenter were accumulated during the last 250 ka at a mean rate of 2.2–2.4 m kyr− 1. Long piston coring in the central Gulf of Corinth basin enabled the recovery of lacustrine sediments, buried beneath 12–13.5 m of Holocene marine sediments. The lacustrine sequence consists of varve-like muddy layers interbedded with silty and fine sand turbidites. AMS dating determined the age of the marine–lacustrine interface (reflector Z) at about 13 ka BP. Maximum sedimentation rates of 2.4–2.9 m kyr− 1 were calculated for the Holocene marine and the last glacial, lacustrine sequences, thus verifying the respective rates obtained by the sequence stratigraphic interpretation. Recent accumulation rates obtained by the 210Pb-radiometric method on short sediment box cores coincide with the above sedimentation rates. Vertical fault slip rates were measured by using fault offsets of correlated reflector Z. The maximum subsidence rate of the depocenter (3.6 m kyr− 1) exceeds the maximum sedimentation rate by 1.8 m kyr− 1, which, consequently, corresponds to the rate of deepening of the basin's floor. The above rates indicate that the 2.2 km maximum sediment thickness as well as the 870 m maximum depth of the basin may have formed during the last 1 Ma, assuming uniform mean sedimentation rate throughout the evolution of the basin. 相似文献
15.
The results of the 7 years (1994–2000) of monthly monitoring of spring water before and during eruptions show response to volcanic activity. Low salinity and temperature characterize most of the springs, which are located on the flanks of Popocatepetl Volcano. The pH ranges from 5.8 to 7.8 and temperature from 3 to 36 °C. Oxygen and hydrogen isotopic data show that the water is of meteoric origin, but SO 42−, Cl −, F −, HCO 3−, B, and SO 42−/Cl − variations precede main eruptive activity, which is considered linked to influx of magmatic gases and acid fluids that react with sublimates and host rock and mix with the large water system. Na +, Ca 2+, SiO 2 and Mg 2+ concentrations in the water also increased before eruptive activity. The computed partial pressure of CO 2 in equilibrium with spring waters shows values higher than air-saturated water (ASW), with the highest values up to 0.73 bar of pCO 2. Boron is detected in the water only preceding the larger eruptions. When present, boron concentration is normally under health standard limits, but in two cases the concentration was slightly above. Other components are within health standard limits, except for F − in one spring. 相似文献
16.
Rock‐magnetic measurements of two sediment cores from the Madeira Abyssal Plain (MAP), north Atlantic, are used to investigate post‐depositional changes in the concentration, grain size and composition of magnetic minerals in the sediments that have occurred within organic‐rich turbidite horizons. The changes are associated with an initial stage of suboxic (reductive) diagenesis, following depletion of porewater O 2, and a later stage of oxidative diagenesis associated with the slow descent of an oxidation front through the sediment, as a result of diffusion of O 2 from the overlying sea water. The turbidites are of late Quaternary age (δ 18O stages 1–3) and derive both from different sites on the NW African continental margin, and from the flanks of the Canary Islands. Thus, the turbidites are variable compositionally, especially in terms of carbonate, detrital magnetic mineral and organic carbon content. Diagenetic changes in these sediments have been identified using solid‐phase geochemical data (U, Mn, C org and CaCO 3) reported previously in more than one study. Rock‐magnetic parameters of the sediments, when expressed on a carbonate‐free basis, reveal that significant depletion of detrital ferrimagnetic iron (Fe 2+/Fe 3+) oxide grains has occurred within organic‐rich turbidites during redoxomorphic diagenesis. Normalized quotients of magnetic parameters also show that reductive diagenesis is a ferrimagnetic grain size‐selective process, but it has a minimal effect on the canted‐antiferromagnetic Fe 3+ oxides in the sediment. Such components, if present, therefore become relatively enriched in magnetic assemblages as the ferrimagnetic grains are dissolved progressively, and bulk magnetic concentration is thus depleted. There is clear evidence in both cores for the existence of ultrafine ferrimagnetic grains at depth within the suboxic zone of the organic‐rich turbidites, beneath both active and fossil oxidation fronts. These grains are most probably associated with populations of live magnetotactic bacteria, which commonly inhabit such organic‐rich horizons and play a part in the chain of bacterially mediated reactions normally associated with suboxic diagenesis. These results show that simple and rapid rock‐magnetic techniques can be used to characterize early diagenetic processes involving iron phases in deep‐sea sediments, at least as effectively as more laborious, time‐consuming and sample‐destructive geochemical measurements. 相似文献
17.
The behavior of rare earth elements (REE) and Th is studied along the west–east transect at 22°N across the Atlantic Ocean. It is shown that both REE and Th contents, relative to Al (the most lithogenic element), increase toward the pelagic region. The increasing trend becomes more complicated due to variations in the content of biogenic carbonate that serves as a diluting component in sediments. The REE composition varies symmetrically relative to the Mid-Atlantic Ridge (MAR) emphasizing a weak hydrothermal influence on sediments of the ridge axis, although the well-known criteria for hydrothermal contribution, such as Al/(Al + Mn + Fe) and (Fe + Mn)/Ti, do not reach critical values. Variations in the REE content and composition allowed us to distinguish the following five sediment zones in the transect: (I) terrigenous sediments of the Nares abyssal plain; (II) pelagic sediments of the North American Basin; (III) carbonate ooze of the MAR axis; (IV) pelagic sediments of the Canary Basin; and (V) terrigenous clay and calcareous mud of the African continental slope and slope base. Ferromanganese nodules of the hydrogenetic type with extremely high Ce (up to 1801 ppm) and Th (up to 138 ppm) contents occur in pelagic sediments. It is ascertained that P, REE, and Th concentrations depend on Fe content in Atlantic sediments. Therefore, one can suggest that only a minor amount of phosphorus is bound in bone debris. The low concentration of bone debris phosphorus is a result of relatively high sedimentation rates in the Atlantic, as compared with those in pelagic regions of the Pacific. 相似文献
18.
Contamination of groundwater by nitrates leaching from intensive agricultural and livestock operations have become a major concern for surrounding communities that use groundwater as their water supply. High levels of nitrate in drinking water poses a significant risk to human health, i.e., methaemoglobinaemia (“blue baby” syndrome). The traditional pump-and-treat method is ineffective in medium to fine-textured agricultural soils due to the low hydraulic conductivity. This paper presents the results of a laboratory experiment investigating the feasibility of using electrokinetic treatment in retaining, accumulating, moving and remediating nitrates in a silty loam soil under hydraulic gradients. A hydraulic gradient of 1.25 was applied to the horizontal soil columns to simulate a groundwater movement system. The study was performed in two stages. During the first stage of the experiment, the anode located at the inflow end of the columns was able to retard the movement of nitrates even under a hydraulic gradient of 1.25. After 15 days of flow, the effluent nitrate concentration in the control column rose to 90 mg l−1 while no nitrates were detected in the effluent from columns subjected to the electrokinetic treatment. After 15 days, the polarity of the electrodes was switched and this second stage lasted another 20 days. The cathode near the inflow end promoted the conversion of nitrates entering the column to other forms. The anode near the outflow end promoted the migration and accumulation of negatively charged nitrate ions towards the outflow end. By the 12th day, the nitrate concentrations in the electrokinetically treated columns were brought down to <5 mg NO3-N l−1. Electrokinetic treatment retarded nitrate movement against a hydraulic gradient of 1.25 and effectively restored a medium-textured soil contaminated with NO3-N. The NO2-N level remained below 1 mg l−1 throughout the experiment. The hydraulic conductivity varied between 1.0E–7 and 3.6E–7 m s−1. The current requirement varied between 3 and 6 mA. 相似文献
19.
A decrease in temperature (Δ T up to 45.5 °C) and chloride concentration (ΔCl up to 4.65 mol/l) characterises the brine–seawater boundary in the Atlantis-II, Discovery, and Kebrit Deeps of the Red Sea, where redox conditions change from anoxic to oxic over a boundary layer several meters thick. High-resolution (100 cm) profiles of the methane concentration, stable carbon isotope ratio of methane, and redox-sensitive tracers (O 2, Mn 4+/Mn 2+, Fe 3+/Fe 2+, and SO 42−) were measured across the brine–seawater boundary layer to investigate methane fluxes and secondary methane oxidation processes. Substantial amounts of thermogenic hydrocarbons are found in the deep brines (mostly methane, with a maximum concentration up to 4.8×105 nmol/l), and steep methane concentration gradients mainly controlled by diffusive flow characterize the brine–seawater boundary (maximum of 2×105 nmol/l/m in Kebrit Deep). However, locally the actual methane concentration profiles deviate from theoretical diffusion-controlled concentration profiles and extremely positive δ13C–CH4 values can be found (up to +49‰ PDB in the Discovery Deep). Both, the actual CH4 concentration profiles and the carbon-13 enrichment in the residual CH4 of the Atlantis-II and Discovery Deeps indicate consumption (oxidation) of 12C-rich CH4 under suboxic conditions (probably utilizing readily available—up to 2000 μmol/l—Mn(IV)-oxihydroxides as electron acceptor). Thus, a combined diffusion–oxidation model was used to calculate methane fluxes of 0.3–393 kg/year across the brine–seawater boundary layer. Assuming steady-state conditions, this slow loss of methane from the brines into the Red Sea bottom water reflects a low thermogenic hydrocarbon input into the deep brines. 相似文献
20.
深海沉积物中的稀土资源是一种新发现的、潜在的海底稀土资源.对太平洋中部重力活塞取样获得的90个深海粘土样品的矿物组分、常量和稀土化学分析结果进行了系统分析,并与中北太平洋以及西北太平洋南鸟岛附近海域深海沉积物稀土元素地球化学特征进行了对比.研究结果表明:太平洋中部深海粘土以富含沸石、富P及富REY为特征,其碎屑矿物中含有较多的鱼牙骨,其P 2O 5与CaO之间、P 2O 5、CaO与∑REY之间呈良好的正相关关系;其稀土分布模式表现为明显的Ce负异常、一定程度的重稀土元素富集和Y正异常.太平洋中部深海粘土REY富集的主要原因是深海粘土中含有过量的磷酸盐组分,推测过量的磷酸盐组分是由于深海粘土中鱼牙骨碎屑的加入引起的.在北太平洋海域,未受到热液活动影响的条件下,富REY的深海沉积物的稀土元素富集机制具有统一性和普遍性,可以归纳为深海沉积物中高REY磷酸盐的混入作用. 相似文献
|
