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1.
Concretions cemented mainly by siderite, Mg-calcite and iron monosulphide are common in late Holocene marsh and sandflat sediments on parts of the north Norfolk coast. Field experiments have shown that the concretions are actively forming in reduced sediments in which sulphate-reducing bacteria are active. δ13C values ranging from ?3 to ?11·8% (mean ?5·9%0) suggest that the carbonate in the concretions is derived partly from marine sources and partly from microbial degradation of organic matter. δ18O values ranged from ?6·4% to + 0·8% (mean ?1·0%) suggesting that carbonate precipitated in porewaters ranging from pure sea water to-sea water diluted with meteoric water. Chemical analysis of porewaters showed no evidence of significant sulphate depletion at the depth of concretion formation. Some concretions have formed around fragments of wood or metal, but others contain no apparent nucleus. In field experiments siderite, FeS and Mg-calcite were precipitated around several different nuclei within a period of six months. We suggest that siderite may form wherever the rate of iron reduction exceeds the rate of sulphate reduction, such that insufficient dissolved sulphide is available to precipitate all the available dissolved ferrous iron.  相似文献   

2.
Carbonate concretions from the Jet Rock (Upper Lias, Lower Jurassic) of NE England grew in uncompacted sediment, close to the sediment surface. Microbiological activity created isolated microenvironments in which dissolved carbonate and sulphide species were produced more rapidly than they could be dispersed by diffusion, so establishing the localised supersaturation of calcite and metastable iron sulphides. Precipitation of these minerals in the microenvironment formed a single concretion.Mass-balance calculations demonstrate that at least two different microbiological processes participated in concretionary growth. The early growth stages had an unidentifiable microbiological source of carbonate which declined in importance relative to sulphate reduction as growth proceeded. It is suggested that the diffusion of dissolved organic material was important in sustaining microbiological activity.Mineralogical zonations in the concretions result from changes in the chemistry of the microenvironment due to variations in the rates of addition/removal Ca2+, Fe2+, HCO?3 and HS? by microbiological activity, the crystallization of authigenic minerals and diffusion between the microenvironment and surrounding pore waters. Such changes are of only local significance and the resulting mineralogical zonations in a concretion cannot be used to deduce successive stages of diagenesis in the whole sediment.  相似文献   

3.
The crystallographic fabric of siderite in siderite concretions has been determined for upper Carboniferous (Westphalian‐A) non‐marine concretions and lower Jurassic (Pliensbachian) marine concretions. Compositional zoning indicates that individual siderite crystals grew over a period of changing pore water chemistry, consistent with the concretions being initially a diffuse patch of cement, which grew progressively. The siderite crystallographic fabric was analysed using the anisotropy of magnetic susceptibility, which is carried by paramagnetic siderite. The siderite concretions from marine and non‐marine formations exhibit differences in fabric style, although both display increases in the degree of preferred siderite c‐axis orientation towards the concretion margins. The Westphalian non‐marine siderites show a preferred orientation of siderite c‐axes in the bedding plane, whereas the Pliensbachian marine siderites have a preferred orientation of c‐axes perpendicular to the bedding. In addition, a single marine concretion shows evidence of earlier formed, inclined girdle‐type fabrics, which are intergrown with later formed vertical c‐axis siderite fabrics. The marine and non‐marine fabrics are both apparently controlled by substrate processes at the site of nucleation, which was probably clay mineral surfaces. Siderite nucleation processes on the substrate were most probably controlled by the (bio?) chemistry of the pore waters, which altered the morphology and crystallographic orientation of the forming carbonate. The preferred crystallographic orientation of siderite results from the orientation of the nucleation substrate. Fabric changes across the concretions partially mimic the progressive compaction‐induced alignment of the clay substrates, while the concretion grew during burial.  相似文献   

4.
A shale split in the well-studied Foord Seam (Upper Carboniferous), Stellarton Basin, Nova Scotia, provides a rare opportunity to study little known siderite concretions with anatomically preserved plants from a limnic basin. Siderite concretions occur throughout the split, commonly as sheet-like, inter-connected lepidodendrid logs, or less frequently as spherical masses; they are typically vuggy. A sample of 14 stratigraphically oriented concretions in the split shows that primary siderite varies from 45% to 80% (wt.%) due to selective replacement by 5% to 40% ferroan dolomite or ankerite in plant tissues. These two minerals show large Mg/Fe and Mg/Ca variability and are Fezoned. Clay content ranges from trace to 20%, and quartz from 5% to 10%. Partial cell-wall destruction by erosion and changeable oxic/anoxic conditions, prior to siderite permineralization, resulted in preservation mainly of the more resistant plant tissues. On average, carbon from siderite is isotopically heavier (+4.8±1.9 0/00) than that from ‘dolomite' (−7.2±1.1 0/00). The distribution of and the positive correlation between δ13C and δ18O probably reflects the two fractionation processes associated with methanogenesis and ‘dolomitization', respectively, in the genetic history of the siderite concretions in the split. Siderite concretions formed diagenetically early from bicarbonate under reducing conditions in a slightly alkaline freshwater environment that precluded calcite deposition.  相似文献   

5.
Septarian concretions in the Staffin Shales Formation (Kimmeridgian, Isle of Skye) allow controls on concretion rheology and septarian cracking to be investigated. Stratabound concretions consist of anhedral ferroan calcite microspar enclosing clay and minor pyrite. Intergranular volumes range from 77% to 88%, and calcite δ13C and δ18O values in most concretion bodies range from ?10·0‰ to ?17·3‰ and +0·3‰ to ?0·6‰ respectively, consistent with rapid and pervasive cementation in marine pore fluids. Septarian rupture occurred during incipient cementation, with a sediment volume reduction of up to 43%. Crack‐lining brown fibrous calcite records pore fluid re‐oxygenation during a depositional hiatus, followed by increasing Fe content and δ13C related to bacterial methanogenesis. Brown colouration results from an included gel‐like polar organic fraction that probably represents bacterially degraded biomass. A new hypothesis for concretion growth and septarian cracking argues that quasi‐rigid ‘proto‐concretions’ formed via binding of flocculated clays by bacterial extracellular polysaccharide substances (EPS). This provided rheological and chemical conditions for tensional failure, subcritical crack growth, volume contraction, calcite nucleation, and incorporation of degraded products into crack‐lining cements. Bacterial decay of EPS and syneresis of host muds provided internal stresses to initiate rupture at shallow burial. Development of septarian (shrinkage) cracks in muds is envisaged to require pervasive in situ bacterial colonization, and to depend on rates of carbonate precipitation versus EPS degradation and syneresis. Subsequent modification of septarian concretions included envelopment by siderite and calcite microspar, hydraulic fracturing associated with Cretaceous shallow burial or Palaeogene uplift; and cementation by strongly ferroan, yellow sparry calcite that records meteoric water invasion of the host mudrocks. An abundance of fatty acids in these spars indicates aqueous transport of organic breakdown products, and δ13C data suggest a predominantly methanogenic bicarbonate source. However, the wide δ18O range for petrographically identical cement (?1·3‰ to ?15·6‰) is difficult to explain.  相似文献   

6.
Carbonate concretions, lenses and bands in the Pleistocene, Palaeogene and Upper Triassic coalfields of Japan consist of various carbonate minerals with varied chemical compositions. Authigenic carbonates in freshwater sediments are siderite > calcite > ankerite > dolomite >> ferroan magnesite; in brackish water to marine sediments in the coal measures, calcite > dolomite > ankerite > siderite >> ferroan magnesite; and in the overlying marine deposits, calcite > dolomite >> siderite. Most carbonates were formed progressively during burial within a range of depths between the sediment-water interface and approximately 3 km. The mineral species and the chemical composition of the carbonates are controlled primarily by the initial sedimentary facies of the host sediments and secondarily by the diagenetic evolution of pore water during burial. Based on the regular sequence and burial depth of precipitation of authigenic carbonates in a specific sedimentary facies, three diagenetic stages of carbonates are proposed. Carbonates formed during Stage I (< 500 m) strongly reflect the initial sedimentary facies, e.g. low Ca-Mg siderite in freshwater sediments which are initially rich in iron derived from lateritic soil on the nearby landmass, and Mg calcite and dolomite in brackish-marine sediments whose pore waters abound in Ca2+ and Mg2+ originating in seawater and calcareous shells. Carbonates formed during Stage II (500–2000 m) include high Ca-Mg siderite, ankerite, Fe dolomite and Fe–Mg calcite in freshwater sediments. The assemblage of Stage II carbonates in brackish-marine sediments in the coal measures is similar to that in freshwater sediments. This suggests similar diagenetic environments owing to an effective migration and mixing of pore water due to the compaction of host sediments. Carbonates formed during Stage III (> 2000 m) are Fe calcite and extremely high Ca-Mg siderite; the latter is exclusively in marine mudstones. The supply of Ca is partly from the alteration of silicates in the sediments at elevated burial temperatures. After uplift, calcite with low Mg content precipitates from percolating groundwater and fills extensional cracks.  相似文献   

7.
Previous studies show the importance of iron- and arsenate-reducing bacteria in mobilizing arsenic in groundwater. Here the authors present experimental evidence of arsenic mobilization in connection with bacterially mediated manganese reduction in groundwater affected by mining activities. Manganese-reducing Pseudomonas species were enriched, isolated and identified by 16S rRNA gene phylogeny from groundwater containing high co-dissolved arsenic (as AsIII) and manganese. Enrichment cultures dissolved synthetic birnessite and hausmannite efficiently, but Mn reduction by isolates was reduced at the upper range of environmental levels of dissolved AsIII. Results suggest either a self-limiting release of arsenic coupled to bacterial manganese reduction, in the absence of other electron donors like sulfide, or increased arsenic resistance conferred to Mn-reducing bacteria in consortia.  相似文献   

8.
Iron‐bearing concretions are valuable records of oxidation states of subsurface waters, but the first concretions to form can be altered drastically during later diagenetic events. Distinctive concretions composed of heavy rinds of iron oxide that surround iron‐poor, mud‐rich cores are common along bases of fluvial cross‐bed sets of the Cretaceous Dakota Formation, Nebraska, USA. Concretion rinds thicken inward and cores contain 46 to 89% void space. Millimetre‐scale spherosiderites are abundant in palaeosols that developed in floodplain facies. Evolution of rinded concretions began when intraformational clasts were eroded from sideritic soils, transported, abraded and deposited in river channels. Alteration of siderite and formation of rinds occurred much later, perhaps in the Quaternary when sandstone pore waters became oxic. Dakota concretions are analogous to ‘rattlestones’ in Pleistocene fluvial channels of The Netherlands, and their rinded structure is analogous to that of iron‐rich concretions in the aeolian Navajo Sandstone of Utah. In all three deposits, rinded concretions formed when pre‐existing, siderite‐cemented concretions were oxidized within a sand matrix. Unlike fluvial examples, siderite in the Navajo Sandstone was autochthonous and of late diagenetic origin, having precipitated from carbon dioxide and methane‐enriched waters moving through folded and jointed strata. Iron‐rich rinds formed in all these strata because concretion interiors remained anaerobic, even as oxygen accumulated in the pore waters of their surrounding, permeable matrix. Iron oxide first precipitated at redox boundaries at concretion perimeters and formed an inward‐thickening rind. Acid generated by the oxidation reaction drove siderite dissolution to completion, creating the iron‐poor core. Iron‐oxide rinds are indicators of the former presence of siderite, a mineral that forms only under reducing conditions, during either early or late diagenesis. Siderite is vulnerable to complete oxidation upon exposure, so the distinctive rinded concretions are valuable clues that aid in deciphering diagenetic histories and for recognizing methanic floodplain palaeoenvironments and wet palaeoclimate.  相似文献   

9.
针对太湖发现由菱铁矿组成的“铁质溅射物”和“贫铁溅射物”是太湖形成于陨石冲击的观点,本文对这些实为铁
质结核样品进行了详细的矿物学、地球化学和年代学测试。数据表明,这些样品是在太湖现代沉积淤泥层中形成的菱铁矿
和褐铁矿结核。结核中含有大量水生植物碎片、植物蛋白石、细菌和少量动物壳体碎片。菱铁矿高温灼烧后全部变成赤铁
矿,说明太湖地区不存在菱铁矿熔融状的高温相。菱铁矿14C测年结果表明各个样品形成于年代,不是瞬间形成的。δ13C 数
据指示为淡水无机碳来源,并非湖区碳酸盐岩直接来源。所谓的“贫铁溅射物”实际是黄土层的成岩钙结核。这些证据表明,
太湖发现的这些结核是沉积成岩期的产物,并非冲击高温溅射熔融形成的溅射物。  相似文献   

10.
Soils in New Zealand, and elsewhere, often contain substantial zones of ferro-manganese concretions and pans (laterally continuous layers) that can affect soil quality and management. Soils containing concretions and pans from Southland, New Zealand, were investigated to determine links between microbial ecology and geochemistry. Three soil profiles were sampled at 100-mm intervals to a depth of 1 m and then assayed for nine different populations of bacteria using selective media. Geochemical analysis was performed on the soils at the same intervals, and on shallow groundwater from nearby wells. The largest concentrations of iron (Fe) and manganese (Mn) coincide with concretions. Nitrogen (N) and carbon (C) are not correlated with Fe and Mn but may be depleted due to bacterial metabolism. Fe and Mn concentrations in groundwater are low, suggesting that the source of these elements in the concretions and pans is in situ weathering rather than groundwater. Numbers of iron oxidising organisms increase where concretions and pans are encountered, but manganese-oxidising organisms decrease. Heterotrophic, sulphur-oxidising, and anaerobic populations have relatively consistent numbers at all depths within the profiles. Fifty organisms were selected for phylogenetic characterisation, of which only Pseudomonas sp. is known to have significant interactions with Fe and Mn. These results suggest a link between concretion development and iron-oxidising microbial populations.  相似文献   

11.
太湖冲击坑溅射物的发现及其意义   总被引：3，自引：3，他引：0  
太湖冲击成因说由来已久,但始终未成定论。近几年在太湖及周边湖泊的淤泥层中发现了许多形态各异的奇石,经多种方法测试研究,确定为太湖冲击坑的溅射物。根据成份,溅射物分为两大类。一类富铁质,以菱铁矿及其胶结的碎屑为主,包括微小球粒、棍状及各种形态的块状和片状体 ;另一类贫铁质,以方解石及其胶结的长英质碎屑为主,碎屑为锐角状的石英晶屑及少量粘土和长英质岩屑。溅射物的大小从厘米级块体到毫米级球粒,再至微米级尘粉都有。溅射物外形多具有旋转扭曲形态及熔壳特征,显示了熔融、塑性- 半塑性特征。这些特征显示其成因经历了冲击震碎、熔融、挖掘抛射、空中飞行,最后溅落在冲击坑及其周围。溅射物的成分反映了太湖靶岩基岩岩性特征。太湖冲击坑溅射物的发现是继太湖诸岛石英砂岩中石英晶体的冲击变质微结构发现之后,又一重大突破。综合其它特征,可以确定太湖为一冲击坑。  相似文献   

12.
《Sedimentary Geology》2006,183(1-2):15-30
Carbonate concretions in the Miocene sedimentary rocks of the Yeonil Group in the Pohang Basin (Korea) were investigated in terms of stable oxygen and carbon isotope composition to delineate the origin and associated diagenetic environment for their formation. Carbonate concretions are widely distributed in all the sedimentary rocks in the Pohang Basin, showing that the calcitic concretions are preserved within the mass-flow deposits and the dolomitic ones mostly in the hemipelagic siliceous rocks (diatomites). Concretions can be classified into four different types, on the basis of the stable isotopic signatures, each of which represents its own geochemical range.Type I concretions are calcitic and are composed of micrite to microspar. They occur in the conglomerates and sandstones which were deposited by mass flows (debris flow to turbidity current). It shows relatively lower δ18O (− 14.0 to − 9.3‰) and δ13C (− 19.6 to − 8.4‰) values. These concretions grew in a sulfate reducing zone under the influence of residual ambient seawater which had been significantly modified by volcanogenic sediments. Type II concretions are also calcitic, composed mostly of micrite with minor microspar and found in the sandstones. These concretions are characterized by relatively high δ18O (+ 1.8 to + 2.4‰) and variable δ13C (− 17.3 to − 0.4‰) values. These isotopic signatures reflect that Type II concretions formed from just beneath the sediment/water interface down to the sulfate reducing zone through the early stage of methanogenesis. Type III concretions are also calcitic, and composed largely of micrite with a minor contribution of microspar. They are observed in hemipelagic mudrocks which were deposited under the influence of mass flows. They are characterized by intermediate to high δ18O (− 4.6 to + 1.6‰) and high δ13C (− 1.3 to + 8.8‰) values. These concretions grew in a methanogenic zone by residual ambient seawater and/or seawater slightly modified by reaction with volcanogenic sediments. Type IV concretions are dolomite with calcite inclusion, and occur in hemipelagic siliceous rocks. These concretions are mostly composed of micrite and characterized by variable δ18O (− 9.1 to + 0.7‰) and high δ13C (+ 3.1 to + 17.9‰) values, suggesting formation in the methanogenic zone, although the residual ambient seawater is slightly modified by volcanogenic sediments.The same type of the concretions is widely distributed throughout the basin and always shows its own distinctive stable isotopic signature. This means that the formation of the given type depends upon the lithology and composition of host sediments that are closely related to the depositional process of the fan-delta systems regardless of their localities. Further, the different types of concretions are also found at the different, but closely spaced stratigraphic levels in the same locality, displaying the distinctive diagenetic conditions for each type. Such preservation of the unique diagenetic signatures in individual type of concretion suggests that the concretions formed in a completely closed diagenetic system. Therefore, caution should be made to simplify and generalize the diagenetic condition for the formation of any concretions in a large sedimentary basin.  相似文献   

13.
Thirty-nine samples of both cold and thermal karst groundwater from Taiyuan, northern China were collected and analyzed with the aim of developing a better understanding of the geochemical processes that control the groundwater quality evolution in the region’s carbonate aquifers. The region’s karst groundwater system was divided into three geologically distinct sub-systems, namely, the Xishan Mountain karst groundwater subsystem (XMK), the Dongshan Mountain karst groundwater subsystem (DMK) and the Beishan Mountain karst groundwater subsystem (BMK). Hydrochemical properties of the karst groundwaters evolve from the recharge zones towards the cold water discharge zones and further towards the thermal water discharge zones. In the XMK and the DMK, the hydrochemical type of the groundwater evolves from HCO3-Ca·Mg in the recharge - flow-through zone, to HCO3·SO4-Ca·Mg/SO4·HCO3-Ca·Mg in the cold water discharge zone, and further to SO4-Ca·Mg in the thermal water discharge zone. By contrast, the water type changes from HCO3-Ca·Mg to HCO3·SO4-Ca·Mg in the BMK, with almost invariable TDS and temperatures all along from the recharge to the discharge zone. The concentrations of Sr, Si, Fe, F− and of some trace elements (Al, B, Li, Mn, Mo, Co, Ni) increase as groundwater temperature increases. Different hydrogeochemical processes occur in the three karst groundwater sub-systems. In the XMK and the DMK, the geochemical evolution of the groundwater is jointly controlled by carbonate dissolution/precipitation, gypsum dissolution and dedolomitization, while only calcite and dolomite dissolution/precipitation occurs in the BMK without dedolomitization. The hydrogeochemical data of the karst groundwaters were used to construct individual geochemical reaction models for each of the three different karst groundwater sub-systems. The modeling results confirm that dedolomization is the major process controlling hydrochemical changes in the XMK and the DMK. In the thermal groundwaters, the dissolution rates of fluorite, siderite and strontianite were found to exceed those of the cold karst groundwater systems, which can explain the higher concentrations of F−, Fe and Sr2+ that are found in these waters.  相似文献   

14.
陈成业  王钦贤  陈多福 《沉积学报》2022,40(6):1691-1701
菱铁矿很好地记录了过去地质流体的信息,能够用于示踪生物地球化学反应相关的成岩作用带。台湾国姓地区中新世海相泥页岩中发育自生的菱铁矿结核,其成因尚未厘清。野外观察发现菱铁矿以不连续透镜体平行散布于泥页岩中,主要由自生碳酸盐菱铁矿（78.63%）等矿物组成。菱铁矿的稀土元素配分模式为轻稀土亏损、中稀土富集,无Ce异常,指示菱铁矿形成于弱氧化的沉积环境,弱氧化的环境促进了菱铁矿在次氧化带的沉淀。菱铁矿的δ13CVPDB和δ18OVPDB值分别为-3.69‰~+0.08‰和-1.09‰~+0.25‰,指示菱铁矿形成于次氧化带,碳源很可能是海水和有机质降解混合产生。研究表明自生菱铁矿能够被用于识别沉积物中的生物地球化学过程和指示成岩作用带。  相似文献   

15.
To better understand the sources and mobilization processes responsible for arsenic enrichment in groundwater in the central part of Datong Basin where serious arsenic poisoning cases have been reported, hydrochemical characteristics of the groundwater and the geochemical and mineralogical features of the aquifer sediments were studied. The aqueous arsenic levels are strongly depth-dependent in the study area and the high arsenic concentrations are found at depths between 15 m and 60 m, with a maximum up to 1820 μg/L. The hydrochemical characteristics of high arsenic groundwater from the Datong Basin indicate that the mobilization of arsenic is related to reductive dissolution of Fe oxides/oxyhydroxides and/or desorption from the Fe oxides/oxyhydroxides at high pH (above 8.0). The bulk chemical results of sediments show the arsenic and iron are moderately correlated, suggesting that arsenic is associated with iron-bearing minerals. Results of sequential-extraction experiment show that solid-phase arsenic is similarly distributed among the different pools of reservoir in the aquifer sediments. Strongly adsorbed arsenic and co-precipitated arsenic are its dominant species in the solid-phase. Geochemical studies using chemical analysis, X-ray diffraction and scanning electron microscopy on magnetically separated fractions demonstrate that iron oxides/oxyhydroxides with residual magnetite and chlorite, illite, iron oxides/oxyhydroxides-coated quartz and feldspar, and ankerite are the dominant carriers of arsenic in the sediments. The major processes of arsenic mobilization are probably linked to desorption of As from Fe oxides/oxyhydroxides and reductive dissolution of Fe-rich phases in the aquifer sediments under reducing and alkaline conditions.  相似文献   

16.
This report describes a new form of arsenian pyrite, called As3+-pyrite, in which As substitutes for Fe [(Fe,As)S2], in contrast to the more common form of arsenian pyrite, As1−-pyrite, in which As1− substitutes for S [Fe(As,S)2]. As3+-pyrite has been observed as colloformic overgrowths on As-free pyrite in a hydrothermal gold deposit at Yanacocha, Peru. XPS analyses of the As3+-pyrite confirm that As is present largely as As3+. EMPA analyses show that As3+-pyrite incorporates up to 3.05 at % of As and 0.53 at. %, 0.1 at. %, 0.27 at. %, 0.22 at. %, 0.08 at. % and 0.04 at. % of Pb, Au, Cu, Zn, Ni, and Co, respectively. Incorporation of As3+ in the pyrite could be written like: As3++yAu++1-y(□)⇔2Fe2+; where Au+ and vacancy (□) help to maintain the excess charge. HRTEM observations reveal a sharp boundary between As-free pyrite and the first overgrowth of As3+-pyrite (20-40 nm thick) and co-linear lattice fringes indicating epitaxial growth of As3+-pyrite on As-free pyrite. Overgrowths of As3+-pyrite onto As-free pyrite can be divided into three groups on the basis of crystal size, 8-20 nm, 100-300 nm and 400-900 nm, and the smaller the crystal size the higher the concentration of toxic arsenic and trace metals. The Yanacocha deposit, in which As3+-pyrite was found, formed under relatively oxidizing conditions in which the dominant form of dissolved As in the stability field of pyrite is As3+; in contrast, reducing conditions are typical of most environments that host As1−-pyrite. As3+-pyrite will likely be found in other oxidizing hydrothermal and diagenetic environments, including high-sulfidation epithermal deposits and shallow groundwater systems, where probably kinetically controlled formation of nanoscale crystals such as observed here would be a major control on incorporation and release of As3+ and toxic heavy metals in oxidizing natural systems.  相似文献   

17.
The evolution of groundwater chemistry along the direction of groundwater flow was studied using hydrochemical data from samples collected along a flow line in the Neogene Aquifer, Belgium. Infiltrating water was found to have a very low mineral content and low pH because the sediments are strongly decalcified. Increasing SiO2 and cation concentrations along the groundwater flow line indicate silicate-weathering processes, confirmed with the aid of saturation indices, calculated with PHREEQC, and stability diagrams. A classification system based on redox sensitive species was developed and shows that an extensive redox sequence is present in the aquifer. At a shallow depth, pyrite oxidation has caused an increase in sulphate, while iron is precipitated as hydroxides. Elevated arsenic concentrations are related to the reduction of these iron hydroxides at a relatively shallow depth and to the dissolution of siderite at greater depth. Dissolution of carbonate in the aquifer material, present in deep layers and to the north, has lead to increased Ca2+ and HCO3 ? concentrations. The Ca2+ from the groundwater is exchanged for Na+, Mg2+ and K+ adsorbed to the clay surfaces at the bottom of the groundwater reservoir. Although the Neogene Aquifer is well flushed, there are still some marine influences present in the deepest parts.  相似文献   

18.

The relevance of groundwater hydrogeochemistry to explain the occurrence and distribution of arsenic in groundwater is of great interest. The insightful discussions on the control of shallow groundwater (< 50 m) hydrogeochemistry in arsenic mobilization are known to be a viable tool to explain the arsenic menace in shallow groundwater. The present investigation emphasizes the hydrogeochemical driver and/or control over the reductive dissolution of Fe-bearing host minerals and thereby releasing arsenic into the shallow groundwater of the study area. The study suggests that hydrogeochemical evolution is mainly governed by carbonate minerals dissolution, silicate weathering, and competitive ion-exchange processes in the shallow aquifers (< 50 m). The present study also indicates the prevalence of carbonate minerals dissolution over silicate weathering. The emergence of Cl− concentration in the shallow groundwater founds the possibilities of anthropogenic inputs into the shallow aquifers (< 50 m). The reducing environment in shallow aquifers (< 50 m) of the study area is evident in the reductive dissolution of Fe- bearing shallow aquifer minerals which absorb arsenic in the solid phase and mobilize arsenic onto shallow groundwater. The study opted for many statistical approaches to delineate the correlation among major and minor ionic constituents of the groundwater which are very helpful to understand the comprehensive mechanism of arsenic mobilization into shallow groundwater.

  相似文献   

19.
Carbonate concretions provide unique records of ancient biogeochemical processes in marine sediments. Typically, they form in organic‐rich mudstones, where a significant fraction of the bicarbonate required for carbonate precipitation is supplied from the decomposition of organic matter in the sediments. As a result, carbonates that comprise concretions are usually characterized by broad ranges in δ13C and include values that are significantly depleted relative to seawater. This article reports results from a physical, petrographic and geochemical analysis of 238 concretions from the Wheeler Formation (Cambrian Series 3), Utah, USA, which are unusual in several respects. Most prominently, they formed in organic‐poor mudstones (total organic carbon = 0·1 to 0·5%) and are characterized by a narrow range of δ13C that onlaps the range of contemporaneous seawater values. Subtle centre to edge trends in δ13C demonstrate that concretion precipitation was initiated by local chemical gradients set up by microbial activity in the sediments, but was sustained during growth by a large pool of inorganic bicarbonate probably derived from alkaline bottom waters. The large inorganic pool appears to have been important in facilitating rapid precipitation of the concretion matrix, which occurred via both displacive and replacive carbonate precipitation during early diagenesis. Stable isotope data from cogenetic pyrite (δ34S) and silica (δ18O) phases provide insight into the evolution of biogeochemical processes during concretion growth, and suggest that concretions were formed almost entirely during sulphate reduction, with only minor modification thereafter. Concretions of the Wheeler Formation appear to represent an end‐member system of concretion formation in which rapid growth was promoted by ions supplied from sea‐water. As such, they offer insight into the spectrum of processes that may influence the growth of carbonate concretions in marine sediments.  相似文献   

20.
The zeolite minerals characterized with hydrated aluminosilicates, negative ionic charge and 3D framework structure are well known for purifying the groundwater occurring in basaltic aquifer systems. However, the filtering mechanism at in situ field conditions is a complex process, which is rarely studied, and hence, it needs to be demonstrated. This paper explores the mechanism of hydrochemical processes and evolution of natural zeolites associated with basaltic rock to enhance groundwater quality. We present the hydrochemical findings and evolution processes derived from 46 groundwater samples (Nt = 46) belong to zeolitic (Nz = 25) and non-zeolitic (Nnz = 21) zones of a micro-watershed (4.4 km2) beset over basaltic terrain, Deccan Volcanic Province (DVP), India. The groundwater samples collected for one hydrological cycle (pre- and post-monsoons) are examined for major ion chemistry to determine the aqueous solution mechanism and ion-exchange process occurred in zeolitic and non-zeolitic zones. Further, the hydrochemical parameters are appraised by means of dominancy of ions, rock–water interactions, silicate weathering, chloro-alkaline indices, cation-exchange bivariate plots and the mechanism controlling groundwater chemistry. The results show that: 1) the purifying efficiency of zeolites for total ionic strength is observed as 63.85 and 68.58% during pre- and post-monsoons, respectively, 2) the significant reduction (36.51%) in total hardness attributed to the positive trend of chloro-alkaline indices depicting the ion-exchange phenomenon between Na+ and K+ (alkalies) and Ca2+ and Mg2+ (alkali-earth) elements in the zeolitic zone, 3) Gibbs plot shows the rock–water interaction as the predominant mechanism controlling groundwater chemistry in the zeolitic zone, and 4) the groundwater quality parameters from zeolitic zone are found within the permissible limit of WHO drinking water standards.  相似文献   

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