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1.
The size distribution of trace metals (Al, Ag, Cd, Cu, Fe, Mn, Ni, Sr, and Zn) was examined in surface waters of the San Francisco Bay estuary. Water samples were collected in January 1994 across the whole salinity gradient and fractionated into total dissolved (<0.2 μm colloidal (10 KDa–0.2 μm) and < 10 kDa molecular weight phases. In the low salinity region of the estuary, concentrations of colloidal A1, Ag, and Fe accounted for ≥84% of the total dissolved fraction, and colloidal Cu and Mn accounted for 16–20% of the total. At high salinities, while colloidal Fe was still relatively high (40% of the dissolved), very little colloidal Al, Mn, and Cu (<10%) and no colloidal Ag was detectable. Colloidal Zn accounted for <3% of the total dissolved along the estuary, and colloidal Ni was only detectable (<2%) at the river endmember. All of the total dissolved Cd and Sr throughout the estuary consisted of relatively low molecular weight (<10 kDa) species. The relative affinity of metals for humic substances and their reactivity with particle surfaces appear to determine the amounts of metal associated with colloids. The mixing behavior of metals along the estuary appears to be determined by the relative contribution of the colloidal phase to the total dissolved pool. Metals with a small or undetectable colloidal fraction showed a nonconservative excess (Cd, Cu, Ni, and Mn) or conservative mixing (Sr) in the total dissolved fraction, relative to ideal dilution of river water and seawater along the estuary. The salt-induced coagulation of colloidal A1, Fe, and Cu is indicated by their highly nonconservative removal along the salinity gradient. However, colloidal metals with low affinity for humic substances (Mn and Zn) showed conservative mixing behavior, indicating that some riverine colloids are not effectively aggregated during their transport to the sea. While colloidal metal concentrations correlated with dissolved organic carbon, they also covaried with colloidal Al, suggesting that colloids are a mixture of organic and inorganic components. Furthermore, the similarity between the colloidal metal:A1 ratios with the crustal ratios indicated that colloids could be the product of weathering processes or particle resuspension. Distribution coefficients for colloidal particles (Kc) and for large, filter-retained particles (Kd) were of the same magnitude, suggesting similar binding strength for the two types of particles. Also, the dependence of the distribution coefficients on the amount of suspended particulate matter (the so-called particle concentration effect) was still evident for the colloids-corrected distribution coefficient (Kp+c) and for metals (e.g., Ni) without affinity for colloidal particles. 相似文献
2.
Three xenoliths erupted as ejecta during recent violent explosion of Stromboli volcano (Aeolian Islands) were investigated in this paper. They consist of high-temperature mineral association (cordierite, hercynite spinels, sillimanite, ±plagioclase, ±mullite, ±corundum) and abundant glass (10–70 vol.%), and may be classified as buchites. The peraluminous composition of the xenoliths, their trace element distribution and REE patterns support their origin from granulite- and amphibolite-facies metapelites of the Calabrian continental crust, which is considered the crystalline basement beneath Stromboli. Buchites have an isotopic composition comparable to that of Stromboli extrusives and significantly different from that of the Calabrian basement. The glass is generally colourless and has a Si–Al–alkali-rich composition, except for one sample where a Fe–Mg–Ca-rich reddish-brown glass also occurs. These two kinds of glass show complicated textures where patches of reddish-brown glass are often surrounded by plagioclase and/or cordierite or forms streaks and swirls with the colourless glass. Cordierite, plagioclase and oxides have different compositions according to their position in the xenoliths. Ca-rich plagioclase (An72–95), Mg-poor cordierite (Mg-values 47–66) and Al-rich spinels are in the inner portions of the xenoliths and associated with colourless glass; on the contrary, close to the contact with the host lava or associated with coloured glass, cordierite shows higher Mg-values, Ti–Fe-bearing oxides occur and plagioclase is chemically similar to the basalt phenocrysts (An66–71). The abundant and fresh glass and the idiomorphic shape of the high-temperature minerals suggest that the xenoliths were hold in the basaltic magma, before its extrusion, for a significant time to allow their partial or nearly complete melting and subsequent nucleation and growth of new phases. During this stage, the interaction between the anatectic liquid and the basaltic magma affected the original isotopic composition of the xenoliths and, in some cases, produced glass and mineral phases (cordierite, plagioclase and oxides) with different composition. 相似文献
3.
This study deals with the weathering processes operating at the scale of a small catchment (Nsimi-Zoetele, Cameroon) and is focused on the role of organic colloids on mineral weathering and transport of elements in natural waters. Samples of river, spring and groundwaters from Nsimi-Zoetele were filtered through membranes of decreasing pore size (0.22 μm, 0.025 μm, or: 300,000 Da, 5000 Da) to separate colloidal fractions from the truly dissolved one. Major and trace elements and dissolved organic carbon (DOC) were analysed in each fraction. Two kinds of waters can be distinguished in the catchment: clear and coloured waters. Clear waters exhibit low concentrations of major and trace elements and DOC. Elements are carried in these solutions in a true dissolved form except Al and rare earth elements (REEs). By contrast, the higher abundances of Al, Fe and trace elements in coloured waters are controlled by the colloidal fraction. Thermodynamic equilibrium calculations show that clear waters are in equilibrium with kaolinite and iron oxi-hydroxide which are major minerals in the weathered soil. For coloured waters, the aqueous speciation of Ca, Mg, Cu, Fe, Al, La and Th was calculated taking into account the complexes with humic acids. Speciation calculations for Cu, Fe, Al, La, Th show a strong complexation with humic acids, in good agreement with the results of the filtration experiments. By contrast, although filtration experiments show a strong control of major cations by organic matter (for example 75% for Ca), speciation calculations reveal that their complexes with humic ligands do not exceed a few percent of total dissolved elements. This discrepancy is explained as an artefact induced by the organic colloids and occurring during the filtration procedure. Finally, both filtration experiments and speciation calculations show that organic matter plays an important role in natural DOC-rich waters. Organic acids increase significantly the dissolution rates of silicates and oxi-hydroxides and thus the amounts of solutes and of complexed elements leaving the catchment. 相似文献
4.
Vertical profiles from the water column, including the maximum turbidity zone (MTZ) to the consolidated sediment were sampled in September 2000 in the freshwater reaches of the Gironde Estuary during a complete neap tide-spring tide cycle. The vertical distributions of dissolved major redox parameters and metals (Mn, Fe, Cd, Cu, V, Co, Ni, Mo, and U) were determined. Reactive particulate metal fractions were also determined from selective leaching. The studied system is characterized by density layers functioning at different time-scales, consisting of two mobile layers, i.e., the liquid (LM) and the soft mud (SM), overlying consolidated sediments (CS). This results in a three-zone diagenetic regime where (1) O 2 dynamics are fast enough to show depletion in the rapidly mixed LM sequence (tidal time-scale), (2) denitrification occurs on the weekly time-scale mixing SM sequence, and (3) the Mn, Fe, and sulfate cycling occurs in the CS layer (annual time-scale). The studied trace metals show differential behavior during early diagenesis: (1) Cd, Cu, and V are released into pore water preferentially from organic matter in the SM, (2) Co, Ni, and U are released in the CS from Mn and Fe oxides during reductive dissolution, and (3) Mo from both processes. Transient conditions (i.e., oscillations of redox fronts and reoxidation processes), due to the dynamics of the mobile layers, strongly influence the trace metal distributions as inducing resolubilization (Cd, Cu, and Mo). In the CS, authigenic metal phases accumulate, either by direct precipitation with sulfides (Cu, Cd) or co-precipitation with Fe-sulfides (Mo). Microbially mediated reduction of Fe oxides is proposed to control U removal from pore water by reduction of U(VI) to U(IV) at depth. However, a significant fraction of the trace metals is trapped in the sediment in exchangeable forms, and therefore is susceptible to be mobilized due to resuspension of estuarine sediment during strong river flood periods and/or dredging activities. 相似文献
5.
我国相继在多个盆地陆相页岩油勘探中获得突破,展示了良好的发展前景。基于现阶段勘探认识,本文认为陆相页岩油富集主要条件是：(1)稳定且有规模和适宜热成熟度的富有机质页岩是重要物质基础,以TOC含量>2%,最佳为3%～4%、母质类型Ⅰ和Ⅱ 1型为主,R o>0.9%或更高(咸化环境0.8%);(2)有一定容积规模的微纳米孔隙且具脆性的多类储层是重要条件,页岩储层有效孔隙度宜>3%～6%;成岩阶段偏低时,纯页岩段不是中高熟页岩油富集段,致密砂岩和混积岩黏土含量宜<20%;成岩阶段高时,页岩黏土含量可高至40%左右;(3)滞留烃数量大且品质好是重要保证,以S 1>2 mg/g为门限,最佳>4～6 mg/g;气油比>80 m 3/m 3,最佳150～300 m 3/m 3;(4)顶底板具封闭性保持超压且滞留足够多轻-中组分烃类。陆相页岩油分布特征是：(1)有外物质注入的深-半深湖相是页岩油主要富集区;(2)具备“四高... 相似文献
6.
Fractionation by ultra-filtration of the dissolved organic material (DOM) in the River Beaulieu, with typical concentrations of dissolved organic carbon (DOC) of 7–8 mg C/l, showed it to be mainly in the nominal molecular weight range of 10 3–10 5, with 16–23% of the total DOC in the fraction > 10 5. The molecular weight distribution of DOM in the more alkaline River Test (average DOC, 2 mg C/l) was similar. In the River Beaulieu water, containing 136–314 βg Fe/l in ‘dissolved’ forms, 90% or more of this Fe was in the nominal molecular weight fraction > 10 5. Experiments showed that DOM of nominal molecular weight <10 5 could stabilize Fe(III) in ‘dissolved’ forms. The concentrations of ‘dissolved’ Fe in the river water probably reflect the presence of colloidal Fe stabilized by organic material and this process may influence the apparent molecular weight of the DOM. Dissolved. Mn (100–136 βg/l) in the River Beaulieu was mainly in true solution, probably as Mn(II), with some 30% in forms of molecular weight greater than ca 10 4.During mi xing in the Beaulieu Estuary, DOC and dissolved Mn behave essentially conservatively. This contrasts with the removal of a large fraction of the dissolved Fe (Holliday and LISS, 1976, Est. Coastal Mar. Sci. 4, 349–353). Concentrations of lattice-held Fe and Mn in suspended particulate material were essentially uniform in the estuary, at 3.2 and 0.012%, respectively, whereas the non-lattice held fractions decreased markedly with increase in salinity. For Mn the decrease was linear and could be most simply accounted for by the physical mixing of riverborne and marine participates, although the possibility that some desorption occurs is not excluded. The non-linear decrease in the concentration of non-lattice held Fe in particulates reflected the more complex situation in which physical mixing is accompanied by removal of material from the ‘dissolved’ fraction. 相似文献
7.
痕量金属的胶体结合态是海洋中金属的一种相当普遍的存在形式。胶体与痕量金属之间的相互作用影响着痕量金属在海水中的形态、迁移、生物可利用性及其归宿。总结了海洋胶体态金属的存在及其显著性,概述了胶体对金属在河口混合过程中行为的影响,并简要讨论了胶体在海水中痕量金属的固液相分配中的作用。 相似文献
8.
河流输送到海洋的溶解无机碳(DIC)和有机碳(OC)受自然和人为双重因素的影响。了解DIC和OC的年龄、来源和转化,有助于掌握全球碳收支和提高现在以及未来自然和人类对河流碳循环影响的估算精度。本研究以普定岩溶水-碳循环试验场泉(地下水)-池(地表水)耦联系统为研究对象,利用双碳同位素( 13C- 14C)方法,结合水生植物生长和传统水文地球化学特征,揭示了地下水-地表水系统中DIC和颗粒有机碳(POC)的来源及其转化机制。研究发现:(1)泉-池系统中DIC和POC的Δ 14C具有相同的变化趋势,泉水中Δ 14C值低于池水中Δ 14C值,反映后者可能有“较年轻”的CO 2的加入;(2)池水水化学和碳同位素变化由土地利用类型和池中水生植物共同控制;(3)池水中颗粒有机碳(POC)浓度明显高于泉水,且其Δ 14C值表现出与沉水植物和DIC的一致性(表观年龄均为3 200900 a),说明池水POC主要源于池中水生植物光合作用利用了碳酸盐风化产生的老碳(DIC),使新形成的有机质在表观年龄上“偏老”;(4)池水水体内源有机碳对水体POC的贡献在75%以上,内源有机碳通量(以C计)在250 t·km -2·a -1至660 t·km -2·a -1之间,相对于其他土地利用类型,草地对应的地表水系统具有最大的内源有机碳占比和通量,指示了沉水植物控制型浅水水体初级生产对有机碳循环的重要作用。综上,我们认为在岩溶区通过土地利用调整来调控水生植物群落对于增加碳汇具有重要潜力。 相似文献
9.
Data are presented on suspended particles and colloids in groundwaters from the Osamu Utsumi mine and the Morro do Ferro analogue study sites. Cross-flow ultrafiltration with membranes of different pore sizes (450 nm to 1.5 nm) was used to prepare colloid concentrates and ultrafiltrates for analyses of major and trace elements and U- and Th-isotopic compositions. Additional characterization of colloidal and particulate material was performed by ESCA, SEM and X-ray diffraction. The results indicate the presence of low concentrations of colloids in these waters (typically < 500 μg/l), composed mainly of iron/organic species. Minor portions of uranium and other trace elements, but significant fractions of the total concentrations of Th and REE in prefiltered waters (< 450 nm) were associated with these colloids.Suspended particles (> 450 nm), also composed mainly of hydrous ferric oxides and humic-like compounds, show the same trend as the colloids with respect to U, Th and REE associations, but elemental concentrations were typically higher by a factor of 1,000 or more. In waters of low pH and with high sulphate content, these associations are considerably lower. Due to the low concentrations of suspended particles in groundwaters from the Osamu Utsumi uranium mine (typically <0.5 mg/l), these particles carry only a minor fraction of U and the REE (<10% of the total concentrations in unfiltered groundwaters), but a significant, usually predominant fraction of Th (30–70%). The suspended particle load in groundwaters from the Morro do Ferro environment is typically higher than in those from the mine by a factor of 5 to 10. This suggests that U, Th and the REE could be transported predominantly by particulate matter. However, these particles and colloids seem to have a low capacity for migration. 相似文献
10.
The Upper Permian Castile Formation of the Delaware Basin in northwest Texas and New Mexico consists of up to 600 m of evaporites and is subdivided into units of anhydrite overlain by halite. The Castile Formation has commonly been interpreted as a deep-water, deep-basin deposit in which sediments were laid down in several hundred metres of water or brine. Recent textural observations within anhydrite units, in which the thick-bedded anhydrite horizons have been interpreted as being of shallow-water origin, have challenged this assumption. This geochemical study of the oldest anhydrite unit in the Castile Formation (the Anhydrite 1 Member) attempts to resolve some of the problems regarding brine depth and evolution in the basin. The Anhydrite 1 Member has been subdivided into five major cycles on the basis of the distribution of stratigraphic units of thick-bedded anhydrite. Stable isotopic analyses of sulphur from anhydrite, and oxygen and carbon from calcite show that the basin waters were chemically homogeneous during precipitation of anhydrite, and do not indicate any significant input of meteoric, continental-derived waters. Throughout the section studied progressive enrichment of 18O upwards within cored intervals indicates continuous evaporation of the water body. Carbon isotopes appear to indicate fluctuations in organic activity within the cycles. Trace elemental analyses of Fe, Mg, Sr, Mn, Al, Ba, Zn, Pb and Cu from the sulphate fraction of the samples show a very high variability. There is a distinct increase in trace elemental abundances at the tops of cycles which may indicate variations in precipitation kinetics. Analyses of texturally defined cycles show that up-core trends for many of the trace elements correlate with changes in δ18O, indicating a progressive increase in the influence of evaporation. In addition, cyclical variations in trace elemental composition indicate changes in basin conditions with around a 350-year cyclicity. These changes are independent of δ18O values. The geochemical data do not provide conclusive proof of water depth during deposition of the Castile Formation. The data are interpreted as reflecting small-scale changes in conditions of deposition, despite the fact that water input remained essentially constant in terms of chemical composition. 相似文献
11.
Three types of chemically and isotopically distinct pore fluids from the southern San Joaquin basin previously recognized by J.B. Fisher and J.R. Boles also have distinctive 87Sr/ 86Sr ratios and Sr concentrations. Meteoric fluids have stable isotopic compositions which lie on or near the meteoric water line and low chlorinities. Sr concentrations are between 0.01 and 2.6 mg l −1, and 87Sr/ 86Sr ratios range from 0.7061 to 0.7078. Diagenetically modified connate marine fluids have δD-and δ 18O-values more positive than −35‰ and 0‰, respectively, and have chlorinities generally comparable to seawater. Sr concentration are much higher than the meteoric group (16–198 mg l −1), although the 87Sr/ 86Sr ratios (0.7070–0.7081) are not distinctive. Mixed meteoric-modified connate fluids have δD, δ 18O and chlorinity intermediate between the meteoric and modified connate groups. Sr concentrations are also intermediate, between 16 and 22 mg l −1, but 87Sr/ 86Sr ratios (0.7080–0.7087) are generally more radiogenic than either the meteoric or modified connate groups. All of the fluids have 87Sr/86Sr ratios comparable to or lower than Tertiary seawater. Alteration of detrital plagioclase is the probable origin of the low isotopic ratios. Mass-balance calculations based on the Sr data suggest that essentially no transport of Sr occurred during diagenesis of sandstones containing modified connate pore fluids, while large amounts of Sr have been transported out of meteoric reservoirs by fluid flow. The chemically anomalous mixed meteoric-modified connate fluids contain the most radiogenic strontium in the basin. These fluids are spatially associated with major faults, and may represent clay mineral dehydration waters which have been transported upward from greater depth. These results suggest that the three types of fluids identified by Fisher and Boles represent three distinct mass transport regimes: a largely stagnant deep-basin system containing modified connate pore fluids; an actively recharging meteoric system along the basin flanks; and a third system restricted to the southern basin which may be characterized by largescale cross-formational fluid flow, rather than dilution by meteoric waters. 相似文献
12.
Despite of the importance of the aquatic ecosystems as organic matter pools within the global carbon cycle, specific studies in river sediments are still insufficient. This study was carried out in an Atlantic basin where nine sites were selected in the lowest middle stretch of the River. The analyses include total organic carbon, C/N ratios, humus composition (humic, fulvic and humin), A2/A4 and A4/A6 ratios, biologically active organic matter (BAOM), water soluble organic matter (WSOC) and coloured water soluble organic carbon (CWSOC). The results suggested a predominance of allochthonous sources to the organic matter, highly influenced by the land uses together with the river hydrodynamics, namely urban and forest at sites 1, 2 and 9, and agricultural at sites 7 and 8. The 38% of the total organic matter was humic and fulvic acids. The biologically active organic matter, which may act as a proxy of microbial activity, showed a mean value of 0.9% of the total organic matter, showing the lowest values at sites with the highest organic matter total, soluble or coloured. This coloured organic matter represented an average of 3.60% of the total organic matter, and showed the highest visible light absorption at those sites more affected by human activities, close to centres of population (1, 2 and 9). This coloured fraction showed also a high degree of photostability. C/N ratios were less effective to discriminate between allochthonous or autochthonous sources, whereas A4/A6 ratios were effective to estimate variations of autochthonous sources, as it measures the variations of phytopigments of the river bed sediments. 相似文献
13.
This paper reports on the petrology and geochemistry of a diamondiferous peridotite xenolith from the Premier diamond mine in South Africa. The xenolith is altered with pervasive serpentinisation of olivine and orthopyroxene. Garnets are in an advanced state of kelyphitisation but partly fresh. Electron microprobe analyses of the garnets are consistent with a lherzolitic paragenesis (8.5 wt.% Cr2O3 and 6.6 wt.% CaO). The garnets show limited variation in trace element composition, with generally low concentrations of most trace elements, e.g. Y (<11 ppm), Zr (<18 ppm) and Sr (<0.5 ppm). Garnet rare earth element concentrations, when normalised against the C1 chondrite of McDonough and Sun (Chem. Geol. 120 (1995) 223), are characterised by a rare earth element pattern similar to garnet from fertile lherzolite. All diamonds recovered are colourless. Most crystals are sharp-edged octahedra, some with minor development of the dodecahedral form. A number of crystals are twinned octahedral macles, while aggregates of two or more octahedra are also common. Mineral inclusions are rare. Where present they are predominantly small black rosettes believed to consist of sulfide. In one instance a polymineralic (presumably lherzolitic) assemblage of reddish garnet, green clinopyroxene and a colourless mineral is recognised. Infrared analysis of the xenolith diamonds show nitrogen contents generally lower than 500 ppm and variable nitrogen aggregation state, from 20% to 80% of the ‘B’ form. When plotted on a nitrogen aggregation diagram a well defined trend of increasing nitrogen aggregation state with increasing nitrogen content is observed. Carbon isotopic compositions range from −3.6 ‰ to −1.3 ‰. These are broadly correlated with diamond nitrogen content as determined by infrared spectroscopy, with the most negative C-isotopic compositions correlating with the lowest nitrogen contents. Xenolith mantle equilibration temperatures, calculated from nitrogen aggregation systematics as well as the Ni in garnet thermometer are on the order of 1100 to 1200 °C. It is concluded that the xenolith is a fertile lherzolite, and that the lherzolitic character may have resulted from the total metasomatic overprinting of pre-existing harzburgite. Metasomatism occurred prior to, or accompanied, diamond growth. 相似文献
14.
An ultrafiltration procedure has been developed to study the interaction between organic C and Hg species in natural waters, and a pilot study was conducted in the surface waters of the Florida Everglades. Compared to total Hg, CH 3Hg shows different distribution patterns in the suspended particulate, colloidal, and truly dissolved phases. Colloidal forms (0.22 μm, 3 kDa) contain the majority of the total dissolved Hg, while the amount found in the truly dissolved fraction (<3 kDa) is small (about 10%). However, CH 3Hg, which shows strong binding capability with low molecular-weight dissolved organic C, is present almost entirely in the lower molecular-weight fraction of the colloids and in the truly dissolved fraction. Quantitative CH 3Hg data correlate well with those for dissolved organic C, an indication that the organic matter present in the system plays an important role in the fate and transport of organomercury. Distribution coefficients between water and the different-sized fractions of the dissolved organic C were determined for both total Hg and CH 3Hg. Results for total Hg were in general agreement with other reports resulting from studies of molecular size distributions of total Hg in freshwater systems. This is, to the best of our knowledge, the first report of such distribution profiles for CH 3Hg between different-sized fractions of dissolved organic C in natural waters. 相似文献
15.
The speciation and partition of mercury in a macrotidal estuary (Seine estuary, France) was studied in order to explore the role of the high turbidity zone (HTZ) in mercury transfer to the adjacent coastal waters. Water and particles were analyzed to determine the concentrations of various mercury species, including monomethylmercury and the inorganic fraction. The exchangeable particulate mercury, which varies with salinity, and the mercury fraction associated with the amorphous oxyhydroxides were evaluated. The distribution of dissolved mercury species during early mixing suggests non-conservative behavior of organically bound mercury at the head of the estuary. Mercury in the particles covaried positively with suspended particulate matter concentrations up to a threshold, which constitutes the typical mercury load of particles and deposited sediments of the HTZ. This distribution pattern is well explained by a dilution model: a slowly settling, low metal population of particle, characterized by relatively invariant turbidity, becomes admixed with a variable amount of higher metal content particles derived from the resuspension in the HTZ. In addition, in the HTZ, which acts as a degradation reactor for particulate organic matter, particulate mercury concentrations increase with increasing C:N ratios and amorphous oxyhydroxides particles. Mercury reaches the estuarine HTZ mainly associated with the riverine and marine particles, including organic matter and oxyhydroxides, which are temporarily trapped in the HTZ and mixed with autochthonous HTZ particles. The largest particles periodically settle and undergo diagenetic reactions and resuspensions, which lead to their mercury enrichment. Depending upon hydrodynamic conditions, mercury escapes seaward as fine particulate within the plume, partially associated with the oxyhydroxides. A surface complexation model reproduces most of the partitioning observed. In the dissolved phase the model simulation suggests that a very strong ligand must be present to explain the field observations. 相似文献
16.
A model metasomatized lherzolite composition contains phlogopite and pargasite, together with olivine, orthopyroxene, clinopyroxene and spinel or garnet as subsolidus phases to 3 GPa. Previous works established that at ≥1.5 GPa, phlogopite is stable above the dehydration solidus, determined by the melting behaviour of pargasite and coexisting phases. At 2.8 GPa, melts with residual phlogopite+garnet lherzolite mineralogy at 1195 °C and with garnet lherzolite mineralogy at 1250 °C are both olivine nephelinite with K/Na (atomic)=0.51 and K/Na=0.65, respectively. Recent work shows that melting along the dehydration (fluid-absent) solidus of the phlogopite+pargasite lherzolite at pressures <1.5 GPa is very different with the presence of phlogopite, decreasing the solidus below that of pargasite lherzolite. At 1.0 GPa, both phlogopite and pargasite disappear at temperatures at or slightly above the solidus. The compositions of two melts at 1.0 GPa, 1075 °C (with different water contents), in equilibrium with residual spinel lherzolite mineralogy are silica-saturated trachyandesite (5% melt fraction, 3% H 2O) to silica-oversaturated basaltic andesite (8% melt fraction, 4.5% H 2O). Both compositions may be classified as ‘shoshonites’ on the basis of normative compositions, silica-saturation, and K/Na ratio. Decompression melting of metasomatized lithospheric lherzolite with minor phlogopite and pargasite may produce primary ‘shoshonitic’ magmas by dehydration melting at 1 GPa, 1050–1150 °C. Such magmas may be parental to Proterozoic batholithic syenites occurring in Brazil. 相似文献
17.
Samples of authigenic material, sediment overlying water and oxic surface sediment (0–0.5-cm depth) from a perennially oxygenated lacustrine basin were analysed to investigate which solid phases are important for binding a suite of trace elements (Ag, As, Ca, Cd, Cu, Hg, In, methylmercury (MeHg), Mg, Mo, Pb, Sb and Zn). The authigenic material, which was collected with inert Teflon sheets deployed for several years across the sediment–water interface, contained mainly poorly crystallized Fe oxyhydroxides and natural organic matter, presumably humic substances derived from the watershed. Manganese oxyhydroxides were not present in the collected authigenic material due to the slightly acidic condition (pH = 5.6) of the lake that prevents the formation and recycling of these compounds. Conditional equilibrium constants for the adsorption of cationic ( KFe–M) and anionic ( KFe–A) trace elements onto the authigenic Fe oxyhydroxides were estimated from their concentrations in the authigenic material and in bottom water samples. These field-derived values of KFe–M and KFe–A were compared with those predicted by the surface complexation model, using laboratory-derived intrinsic adsorption constants and the water composition at the study site. Equilibrium constants ( KPOM–M) were also calculated for the adsorption of the cationic trace elements onto the humic substances contained in the diagenetic material. The field-derived values of KPOM–M were compared to those predicted by the speciation code WHAM 6 for the complexation of the trace elements by dissolved humic substances in the lake. Combining the results of the present study with those on the distributions of trace elements in the porewater and solid-phase sediments reported in previous studies at the same site, it was determined whether the trace elements bind preferentially to Fe oxyhydroxides or natural organic matter in oxic sediments. The main inferences are that the anionic trace elements As, Mo and Sb, as well as the cationic metal Pb are preferentially bound to the authigenic Fe oxyhydroxides whereas the other trace elements, and especially Hg and MeHg, are preferentially bound to the humic substances. 相似文献
18.
东准噶尔北缘和东天山雅满苏带是中国新疆北部地区两个重要的晚古生代铁氧化物-铜-金矿化潜力区,以老山口、乔夏哈拉和黑尖山矿床作为典型矿床代表。研究表明两区域的铁氧化物-铜-金矿床均产出于盆地闭合的弧盆转化体系下,且具有明显的铁、铜-金两阶段矿化。卤族元素和稀有气体同位素作为可靠的流体示踪剂,被应用于探究这一特定构造环境下的铁氧化物-铜-金矿床的流体演化和矿床成因。结果显示老山口、乔夏哈拉和黑尖山矿床的成矿流体具有明显的混合流体端员特征:(1)岩浆流体端员,主要参与黑尖山矿床磁铁矿阶段,I/Cl、Br/Cl和 40Ar/ 36Ar比值分别为(16.3~18.0)×10 -6、(1.03~1.06)×10 -3和352~437;(2)海水表源蒸发成因盐卤水端员,主要参与老山口矿床铜-金矿化阶段,I/Cl、Br/Cl和 40Ar/ 36Ar比值分别为(77.1~87.7)×10 -6、(1.53~1.80)×10 -3和672~883;(3)蒸发岩溶解或者深度水-岩反应成因的盐卤水/沉积岩地层水端员,主要参与到老山口、乔夏哈拉矿床的磁铁矿阶段以及黑尖山、乔夏哈拉矿床的铜-金矿化阶段,综合I/Cl、Br/Cl和 40Ar/ 36Ar比值分别为(477~26 301)×10 -6、(0.39~1.28)×10 -3和288~510。明显的多阶段矿化和铜-金矿化阶段以非岩浆富Ca高盐度卤水为主的特征与世界范围内的IOCG型矿床极为相似,表明新疆北部的铁氧化物-铜-金矿床应为IOCG型矿床。 相似文献
19.
Bulk chemical, mineralogical and selective leach analyses have been made on a suite of abyssal ferromanganese nodules and associated sediments from the S.W. equatorial Pacific Ocean. Compositional relations between nodules, sediment oxyhydroxides and nearby ferromanganese encrustations are drawn assuming that the crusts represent purely hydrogenetic ferromanganese material. Crusts, δMnO 2-rich nodules and sediment oxyhydroxides are compositionally similar and distinct from diagenetic todorokitebearing nodules. Compared to Fe-Mn crusts, sediment oxyhydroxides are however slightly enriched, relative to Mn and Ni, in Fe, Cu, Zn, Ti and Al, and depleted in Co and Pb, reflecting processes of non-hydrogenous element supply and diagenesis. δMnO 2 nodules exhibit compositions intermediate between Fe-Mn crusts and sediment oxyhydroxides and thus are considered to accrete oxides from both the water column and associated sediments.Deep ocean vertical element fluxes associated with large organic aggregates, biogenic calcite, silica and soft parts have been calculated for the study area. Fluxes associated with organic aggregates are one to three orders of magnitude greater than those associated with the other phases considered, are in good agreement with element accumulation rates in sediments, and are up to four orders of magnitude greater than element accumulation rates in nodules. Metal release from labile biogenic material in surface sediments can qualitatively explain the differences between the composition of Fe-Mn crusts and sediment oxyhydroxides.Todorokite-rich diagenetic nodules are confined to an eastwards widening equatorial wedge. It is proposed that todorokite precipitates directly from interstitial waters. Since the transition metal chemistry of interstitial waters is controlled dominantly by reactions involving the breakdown of organic carbon, the supply and degradation rate of organic material is a critical factor in the formation of diagenetic nodules. The wide range of (trace metal/Mn) ratios observed in marine todorokite reflects a balance between the release of trace metals from labile biogenic phases and the reductive remobilisation of Mn oxide, both of which are related to the breakdown of organic carbon. 相似文献
20.
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
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