The effect of dissolved water on the oxidation state of iron in natural silicate liquids

Ferric-ferrous ratios have been measured in 22 experiments on three natural compositions equilibrated at known temperature (950°–1100° C) and oxygen fugacity, and at water-saturated conditions over a pressure range from 0.05 to 0.2 GPa. There does not appear to be any reaction between the melt and the capsule material that affects the redox state of the iron in the melt. An empirical expression for the anhydrous behavior of the redox state of iron in each of these compositions has also been determined at 1 bar as a function of temperature and oxygen fugacity. A direct comparison of the hydrous ferric-ferrous values with the calculated anhydrous values shows that the dissolution of water in a per-alkaline rhyolite, andesite, and an augite minette has no effect on the redox state of the iron in these melts. This result parallels the effect of water on sulfide speciation in basaltic melts, and confirms published results on experimental hydrous basalts.     

Water and sediment quality assessment in the mid-Black Sea coast of Turkey using multivariate statistical techniques

The aim of this study was to investigate the water and sediment quality in the mid-Black Sea coast of Turkey. The samples were collected from six stations during 2007. Investigated parameters were total carbon (TC), total inorganic carbon (TIC), total organic carbon (TOC), ammonium-nitrogen (NH₄-N), nitrate-nitrogen (NO₃-N), nitrite-nitrogen (NO₂-N), total phosphorus (TP), sulphate, total hardness, methylene blue active substances (MBAS), phenol, adsorbable organic halogens (AOX), dissolved oxygen (DO), pH and electrical conductivity (EC) in water samples and TC, TIC, TOC, TP, pH, electrical conductivity (EC), redox potential (Eh) and water content (WC) in sediment samples. Different multivariate statistical techniques were used to evaluate variations in surface water and sediment quality. Principal component analysis helped in identifying the factors or sources responsible for water and sediment quality variations. Five factors were found responsible for 87.63% of the total variance in the surface waters. In sediments, three factors explained 84.73% of the observed total variance. Cluster analysis classified the monitoring sites into two groups based on similarities of water and sediment quality characteristics.     

Heterogeneous Fe(II) oxidation and zeta potential

The determination of electrophoretic mobility and zeta potential was used as a diagnostic tool, alongside kinetic experiments, to delineate between three plausible mechanisms for the heterogeneous oxidation of Fe(II) by dissolved oxygen. One of these mechanisms is dependant on the positive surface charge that exists on Fe(III) (oxy)hydroxide surfaces at pH values below the Iso-Electric Point (IEP). However, this mechanism can be disputed as catalysis is observed on Fe(III) (oxy)hydroxide surfaces above the IEP despite a negative zeta potential. As well as an IEP shift an overall reduction of the magnitude of the zeta potential is observed in samples of field Fe(III) (oxy)hydroxide collected from the Taff Merthyr mine water treatment site in South Wales, UK. Low zeta potentials determined in mine water treatment systems will have beneficial effects for particle coagulation and settling in passive mine water treatment systems.     

江苏王港潮间带表层沉积物特征及输运趋势

潮滩沉积物粒度参数可以用来反映沉积物沉积的水动力条件和沉积环境。根据对江苏王港潮间带采集的15 4个表层样品的粒度资料进行分析,结果表明,沉积物类型以粉砂为主;随着水动力环境由海向陆的减弱,沉积物粒度参数表现出有规律的变化趋势,即由岸向海粒径具有粗化趋势,分选变好,逐渐正偏并达到近对称。研究区与世界其他地区的潮滩在沉积特征上有较大差异,主要是由于沉积物来源、水动力环境及受生物作用的强弱程度不同所致。沉积物输运趋势分析显示,该地区沉积物输运主要受当地潮波特征、大型人工建筑物、地貌形态及生物作用的影响;在低潮线附近主要向西北方向输运,随着向陆地方向的延伸,沉积物由向西输运逐渐转变为向南输运。     

Grain‐size distributions on high‐energy sandy beaches and their relation to wave dissipation

Grain size and sorting represent two key parameters when characterizing sediments or modelling beach morphology and sediment transport. Traditionally, an average value for grain size or sorting is often assumed for the entire area, determined from only a few sediment samples, ignoring any spatial (or temporal) variability in sediment characteristics. This contribution uses a data set of physical surface sediment samples from 53 beach locations around the south‐west peninsula of the United Kingdom, in addition to bi‐monthly, high spatial resolution (mean 240 samples) digital grain‐size surveys from a high‐energy, oceanic, sandy beach (Perranporth, North Cornwall). Systematic spatial variations in grain size and sorting were consistently observed in the seaward direction across the intertidal zone of sandy beaches, with grain‐sizes coarsening and sorting improving by up to 51·7% and 64·3%, respectively. This variability was deterministically related to the time‐averaged, antecedent‐adjusted energy dissipated by breaking waves, with the observed maximum grain‐size and sorting values correlating with the location of peak wave energy dissipation (r² = 0·998, P < 0·01).     

Pore water geochemistry near the sediment-water interface of a zoned, freshwater wetland in the southeastern United States

 Sediment and its associated pore water were collected from a zoned, freshwater, riparian wetland, located in the Talladega National Forest, northeastern Hale County, Alabama, to study the porewater chemistry and its spatial changes within and between the wetland ecological zones. Obvious changes in pH, Eh and element concentrations were observed between the different wetland ecological zones. Major cations (Ca, Mg, and Na) and trace elements (B, Ba, Sr, and Mn) have very good spatial correlation with Fe and Mn distributions, both in the pore water and the sediment, suggesting that adsorption on, and desorption from, iron and manganese oxyhydroxides are important processes controlling the distributions of these elements in the wetland sediment. However, an equilibrium adsorption model is not able to explain the distribution of trace elements between the pore water and sediment. A redox kinetic model gives similar vertical profiles for iron and the correlated elements as those measured in the field and thus suggests that the relative rates of ferrous iron oxidation and the reductive dissolution of ferric iron in the sediment are important variables determining the distributions of these elements in the wetland pore waters. Received: 31 October 1996 · Accepted: 27 May 1997     

Determination of the Trace Refractory Elements V, Nb and Ta in Environmental Samples by ICP-MS After Separation and Preconcentration with Nanometre-Sized Alumina Microcolumns Following Chemical Modification by Gallic Acid

Nanometre-sized alumina was chemically modified with gallic acid (GA) and used as a solid phase adsorption material for the determination of trace amounts of V, Nb and Ta in natural water, soil and stream sediment samples by inductively coupled plasma-mass spectrometry. The effects of pH, sample flow rate and volume, elution solution and interfering ions on the recovery of the analytes were investigated. The results showed that V, Nb and Ta could be adsorbed at pH 4.0 and recovered with 1 ml of 2.0 mol l^-1 HCl. Under optimised conditions, the adsorption capacity of GA-modified nanometre-sized Al₂O₃ was found to be 7.0, 8.9, 13.3 mg g^-1 for V, Nb and Ta, respectively. The limits of detection were as low as 0.25, 0.24 and 0.66 ng l^-1 for V, Nb and Ta, respectively with a concentration factor of fifty. The recovery of V, Nb and Ta for spiked water samples was between 85.7 and 116%. The developed method has also been applied to the determination of trace V, Nb and Ta in soil and stream sediment certified materials, and the determined values were in a good agreement with the certified values.     

长江口及邻近海域表层沉积物pH、Eh分布及制约因素

使用精密酸度计和新型全自动氧化还原电位仪测定了长江口及其临近海域表层沉积物中的pH、Eh值,分析了它们的分布特征,并从水团性质、层化特征、底质类型、生物扰动等方面深入探讨了pH、Eh的影响因素和影响机理。研究表明:研究区内表层沉积物属于中性—弱碱性环境,pH值变化于7.1～7.8之间,空间分布上具有分带性和不均一性特征;为还原环境,Eh变化于-100～-300 mV之间,大部分在-250 mV左右,其空间分布也具有弱分带和不均一的特点。该区沉积物酸碱性主要受水团性质的制约,同时底质类型、生物扰动对沉积物酸碱性也有一定影响,而氧化还原电位则主要受水团性质、水层层化和生物扰动等的影响。     

Geochemical behavior of arsenic in reducing sulfidic sediments of reservoir contaminated by acid mine drainage

The sediment from an acid mine drainage affected reservoir of Guizhou province of China has the iron and arsenic concentration of about 400 and 2.6 g/kg, respectively. Sediment cores were collected, and were used to study the arsenic behavior in the seriously acidified reservoir from the viewpoint of chemical thermodynamics. The limestone neutralization and ferric iron hydrolysis regulated the porewater pH from about 2.9–5.8. The reductive dissolution of As–Fe-rich (hydr)oxides under the mild acidic conditions was the main mechanism for the release of absorbed arsenic into porewater. The maximum concentrations of iron, sulfate and arsenic reached to about 2,800, 9,000 and 1 mg/l, respectively. Arsenic speciation transformation and hydrous ferric oxide (HFO) crystallization enhanced the arsenic mobility in sediment. In addition, the iron sulfide minerals diagenesis could play a role in removing the dissolved arsenic from porewater. The actual distribution of arsenic concentration in porewater was well simulated using the model of surface complexation of arsenic to HFO. Although arsenic concentration in porewater could be above 100 times higher than that of reservoir water, it was not easy to release into the reservoir water through diffusion, because the shallow sediment had relatively strong arsenic adsorption capacity, and new HFO could be generated continuously at the sediment water interface.     

Arsenic in framboidal pyrite from recent sediments of a shallow water lagoon of the Baltic Sea

Arsenic is a redox‐sensitive element of environmental relevance and often enriched in iron sulphides. Because sediments from the Achterwasser lagoon, a part of the estuarine system of the river Oder, south‐west Baltic Sea, show unexpectedly high pyrite concentrations of up to 7·5 wt% they were used to investigate the influence of authigenic pyrite on the mobility and burial of As in the coastal environment. Micro‐X‐ray‐fluorescence measurements of 106 micrometre‐sized pyrite framboids from the anoxic sediments show highly variable As concentrations ranging from 6 to 1142 μg g^?1. Even within a 1 cm thick layer, the As concentration of different framboids varies greatly and no clear depth trend is visible throughout the 50 cm long sediment core. Pyrite can account for 9 to 55% (average 22%) of the total As budget of the sediments and the degree of trace metalloid pyritization for As ranges from 26 to 61%, indicating that authigenic pyrite formation is an important process in the geochemical cycling of As in coastal sediments. High‐resolution micro‐X‐ray fluorescence mapping of single pyrite grains shows that As is distributed inhomogeneously within larger framboids, suggesting changing pore water composition during pyrite growth. X‐ray absorption near edge structure spectra indicate that As is usually present as As(‐I) substituting S in the pyrite lattice. However, in samples close to the sediment/water interface a considerable part of As is in higher valence states (+III/+V). This can be explained by frequent re‐suspension of the surficial sediments to the oxic water column due to wave action and subsequent re‐deposition, leading to the adsorption of As oxyanions onto pyrite. Although reduced As(‐I) becomes more important in the deeper samples, reflecting decreasing redox potential and a longer time since deposition, the occurrence of oxidized As species (AsIII/AsV) in pyrite in the anoxic part of the sediment suggests formation under dysoxic conditions.     

Investigations on different positions of electrodes and their effects on the distribution of Cr at the water sediment interface

In most mining areas, significant concentrations of metals such as Pb, Cu, Cr, Zn, Cd, Fe, Mn, Co, Ni, Hg, Ar, halogenated organic compounds and radionuclides are found. Of those, Cr is one of the well-known heavy metals that forms toxic species. It is necessary to study the mobilization and accumulation of Cr at the sediment water interface in an electric field at varying different positions and conditions of the electrode arrangement. The tests were carried out with a natural sediment containing heavy metals from the river Weisse Elster (Germany). The electrokinetic experiments have been performed in columns filled with sediment using electrodes made of conductive polymers (polyethylene with carbon black) at a maximum current density of 0.5 mA/cm². The experimental results suggest that the mobilization and accumulation of Cr highly depends on chemical factors for e.g., pH value, redox potential, respectively redox status and the content of Fe, A1 and organic matter in the soil or sediment. The sorption of Cr (III, VI) is very high in the pH range > 4.5. As expected, a high mobilization of Cr (III, VI) was seen in the case of the experiments with the anode at the sediment, because the pH value was lower than mentioned above. On the opposite, the best conditions for the Cr (III, VI) immobilization is high pH values (cathode at the sediment).     

新疆柴窝堡湖沉积物中环境敏感粒度组分揭示的环境信息

通过对柴窝堡湖沉积物剖面和流域表层沉积物进行粒度分析,结合沉积剖面年代序列,研究了柴窝堡地区的环境演变与沙尘暴事件。首先通过主成分因子分析,对柴窝堡湖沉积物剖面粒度不同粒级组分含量进行了研究,探讨了湖泊沉积物的物质来源,获得了两个主控因子F1和F2,它们控制了湖泊沉积物近97.7%的粒度变化特征。研究表明,F2代表了以57 μm为众数粒径的次总体,主要来源于地表风沙侵蚀;而F1为以7 μm为众数粒径的次总体,主要受流水作用控制。进而通过粒径-标准偏差法,提取了湖泊沉积物中环境敏感粒度组分,风成组分C2（20~209 μm）反映了区域风沙活动的历史,并揭示了1910-1930年和1980-2000年为百年来的两个沙尘暴相对活动强烈的时期。沉积物中记录的1980年和2000年左右的沙尘事件与器测记录及历史文献记载具有很好的一致性。最后利用均值突变诊断分析,发现柴窝堡湖地区1910年前后存在近百年来最强的沙尘事件,揭示了近百年来该地区一次最强的环境突变事件。      

古元古代大氧化事件(GOE)前后海洋环境的变化: 来自华北条带状铁建造(BIF)岩相学和地球化学的证据*

条带状铁建造(BIF)是形成于前寒武纪海洋中的化学沉积岩,记录了古海洋氧化还原状态的重要信息。华北克拉通广泛分布的新太古代和古元古代BIF,是了解古元古代大氧化事件(GOE)前后古海洋氧化还原环境变化的理想对象。初步研究表明,华北克拉通新太古代BIF主要为磁铁矿型氧化物相和硅酸盐相,极少数出现碳酸盐相;古元古代BIF包括赤铁矿型和磁铁矿型氧化物相、硅酸盐相和碳酸盐相,其中赤铁矿相是古元古代BIF独有的。以上矿物学特征表明,新太古代和古元古代水体的氧化还原条件是不同的。华北克拉通新太古代BIF的稀土元素组成缺乏强烈的负Ce异常,反映同期海水氧含量非常低,为缺氧状态; 但少量BIF也包含有负Ce异常,同时具有较大变化范围的Th/U值,指示新太古代海洋的局部水体氧含量相对较高,呈弱氧化状态。与新太古代BIF相比,古元古代BIF的Ce异常变化较大,包括无异常、正异常和负异常,尤其是赤铁矿相BIF具明显的负Ce异常,表明古元古代水体的氧含量和氧化还原结构已发生了明显变化; 结合华北克拉通BIF的Ni/Co、V/(V+Ni)和Th/U等比值特征,认为古元古代海洋呈次氧化—氧化环境。新太古代BIF 强烈富集重铁同位素,S同位素非质量分馏效应较为明显;而古元古代BIF相对富集轻铁同位素,S同位素非质量分馏效应不明显。综上,新太古代海洋环境整体缺氧,但局部可能存在氧气“绿洲”,暗示光合产氧作用在太古代晚期已经存在;大氧化事件期间及之后的古海洋总体具上部氧化、下部还原的分层特征。     

海南高隆湾海滩生物碎屑分布及其对沉积物粒度特征的影响

在热带砂质海岸,生物碎屑是海滩沉积物的重要组成部分,其分布和变化影响海滩沉积物的粒度特征。采用添加过量盐酸和双氧水的方法对海南高隆湾海滩表层沉积物进行了去生物碎屑前后粒径分布的对比,并结合海滩高程测量分析,结果表明:（1）海滩剖面上沉积物中生物碎屑的含量主要受到海水动力的影响,且生物碎屑颗粒较粗、重量较大,在高潮时由波浪流推上海滩并滞留。（2）海滩沉积物中生物碎屑的分布主要受三方面影响:一是地形及常涌浪向;二是区域中养殖业产生的生物碎屑;三是岸外发育的珊瑚礁坪。（3）海滩沉积物中生物碎屑的含量随季节变化,冬季至春季由海水供给的生物碎屑减少、进一步分解,使得北部海滩生物碎屑含量减少;而珊瑚碎屑的稳定供给和春季较强的波浪动力条件又使研究区南部断面的生物碎屑含量增加。（4）海滩沉积物中粗颗粒所含生物碎屑多于细颗粒中的生物碎屑,生物碎屑粒径主要为-1~2,即粗砂至细砾。沉积物中生物碎屑含量愈大,对粒径参数的影响也愈大。     

Changes of oceanic environment before and after the Paleoproterozoic Great Oxidation Event(GOE): Evidence from petrography and geochemistry of banded iron formation(BIF)from the North China Craton

Banded iron formation(BIF)belongs to sedimentary rocks formed in Precambrian marine,which can directly reflect the redox state of the ancient oceans. Mineral composition and geochemistry of BIF can reveal the relative changes of oxygen contents of ancient atmosphere-ocean. The Neoarchean and Paleoproterozoic BIFs widely distributed in the North China Craton(NCC),are the ideal research objects for understanding the changes of the ancient ocean redox environment before and after the Paleoproterozoic Great Oxidation Event(GOE). Our previous studies indicated that the sedimentary facies of the Neoarchean BIF in the NCC are mainly magnetite-type oxide and silicate,with minor carbonate. The sedimentary facies of the Paleoproterozoic BIF are hematite- and magnetite-type oxide,silicate and carbonate,of which the hematite-oxide facies is unique to the Paleoproterozoic BIF. The above mineralogical features suggest that the redox conditions of the Neoarchean and Paleoproterozoic seawater are different. The rare earth element composition of the Neoarchean BIF in the NCC lacks a strong negative Ce anomaly,reflecting that the oxygen content of contemporary seawater is very low and the marine is anoxic. However,a small amount of BIFs in the NCC also present the negative Ce anomalies and a wide range of Th/U ratios,indicating that the local water of the Neoarchean ocean had relatively high oxygen content and was at a weak oxidation state. Compared with the Neoarchean BIFs,the Paleoproterozoic BIFs present a wide range of Ce anomalies(i.e.,no Ce anomalies,positive Ce anomalies and negative Ce anomalies). The hematite-bearing BIF has an obvious negative Ce anomalies,implying that the oxygen content and redox state of Paleoproterozoic seawater changed significantly. Combined with the ratios of Ni/Co,V/(V+Ni)and Th/U of the BIFs in the NCC,the Paleoproterozoic oceans exhibited a suboxidation to oxidation environment. Besides,Neoarchean BIF is strongly enriched in heavy iron isotopes and the non-mass fractionation of S isotope is obvious,whereas the Paleoproterozoic BIF is relatively enriched in light iron isotopes and the non-mass fractionation of S isotope is not obvious. It is summarized that the Neoarchean marine is anoxic,but the oxygen‘oasis' may exist locally,implying that photosynthetic oxygen production already existed in the Late Neoarchean. The ancient ocean presented a layered characteristics during and after the GOE,indicating that the shallow water was generally oxidized and the deep water was reduced.     

A comparative study of iron and manganese diagenesis in continental slope and deep sea basin sediments off Uruguay (SW Atlantic)

Pore water and solid phase from surface sediments of the continental slope off Uruguay and from the Argentine Basin (southwestern Atlantic) were investigated geochemically to ascribe characteristic early diagenetic reactions of iron and manganese. Solid-phase iron speciation was determined by extractions as well as by Mössbauer spectroscopy. Both methods showed good agreement ( <6% deviation) for total-Fe speciation. The proportion of easy reducible iron oxyhydroxide relative to total-Fe oxides decreased from the continental slope to the deep sea which is attributed to an increase in crystallinity during transport as well as to a general decrease of iron mobilization. The product of iron reoxidation is Fe oxyhydroxide which made up less than 5% of total Fe. In addition to this fraction, a proportion of smectite bound iron was found to be redox reactive. This fraction made up to 10% of total Fe in sediments of the Argentine Basin and was quantitatively extracted by 1?N HCl. The redox reactive Fe(+II) fraction of smectite was almost completely reoxidized within 24?h under air atmosphere and may therefore considerably contribute to iron redox cycling if bioturbation occurs. In the case of the slope sediments we found concurrent iron and manganese release to pore water. It is not clear whether this is caused by dissimilatory iron and manganese reduction at the same depth or dissimilatory iron reduction alone inducing Mn(+IV) reduction by (abiotic) reaction with released Fe²⁺. The Argentine Basin sediment showed a significant manganese solid-phase enrichment above the denitrification depth despite the absence of a distinct pore-water gradient of Mn. This implies a recent termination of manganese mobilization and thus a non-steady-state situation with respect to sedimentation or to organic carbon burial rate.     

近期长江口-杭州湾邻近海域沉积物粒径的时空变化及其影响因素

为了研究长江口-杭州湾外近海沉积物粒径的现状和近期变化,于2008年4月在该区域用箱式取样器取得了33个表层样,用震动活塞采样器取得7个柱状样;在室内用激光粒度仪对沉积物样品进行了粒度分析并与历史时期的研究成果进行对比。结果表明,1）表层沉积物总体上呈东粗（砂）西细（泥）的特点,粒径总体上的空间格局与历史时期相似;但砂-泥区界线在研究区北部（长江口和杭州湾外）有向西迁移（蚀退）迹象（西移10~30 km）,而在南部（舟山群岛以南）则出现明显向东迁移（淤进）现象（最大超过50 km）。2）当前的表层沉积物形成一条南北连续的泥质带（粒径向南逐渐变细）,反映过去存在于舟山群岛以东的最细组分（“黏土”）带不连续现象在表层现已趋于消失。3）表层沉积物粒径趋势分析揭示长江入海泥沙的运移方向主要是向南-东南。4）泥质区柱状沉积物具有粉砂和黏土为主但在垂向上（反映在时间上）有粗细多变的特点（侵蚀区表层沉积物有粗化迹象）。研究认为,长江口-杭州湾邻近海域现代沉积物对流域和沿海重大人类活动有较敏感的响应。     

长江口崇明东滩沉积物地球化学记录及其环境意义

利用2002年在崇明东滩采得的CDS、CDM和CDN三个典型区域沉积物剖面样品,测定了其中的有机碳、活性铁、总磷以及粒度等特征参数,分析了地球化学元素的分布变化特征并对其沉积环境的变化进行了探讨。结果表明崇明东滩沉积物中有机碳的含量较大(0．3％～1．07％),垂向分布上,表层／亚表层含量高且变化复杂,中下层有机碳含量逐渐变小。Fe3 在整个研究区域均是从表层向下逐渐递减的,Fe2 含量逐渐增加。从实验结果判断,所研究区域沉积环境上层以氧化环境为主,呈弱氧化型,中下层以还原环境为主。总磷含量呈现自上而下减少的变化,CDS表现为波浪形变化。分析发现潮滩沉积物各地球化学元素之间不仅相互作用,并且受到沉积物颗粒大小和水动力、物源输入、物理扰动等因素的影响。崇明东滩沉积物氧化还原界面与中、高潮滩划分界大致相当。     

Geological,mineralogical, and oxygen isotope studies of the Chandmani Uul iron oxide–copper–gold deposit in Dornogobi Province,Southeastern Mongolia

The Chandmani Uul deposit is located in Dornogovi province, Southeastern Mongolia. Iron oxide ores are hosted in the andesitic rocks of the Shar Zeeg Formation of Neoproterozoic to Lower‐Cambrian age. Middle‐ to Upper‐Cambrian bodies of granitic rocks have intruded into the host rocks in the western and southern regions of the deposit. The wall rocks around the iron oxide ore bodies were hydrothermally altered to form potassic, epidote, and sericite–chlorite alteration zones, and calcite and quartz veinlets are ubiquitous in the late stage. Since granitic rocks also underwent potassic alteration, the activity of the granitic rocks must have a genetic relation to the ore deposit. The ore mineral assemblage is dominated by iron oxides such as mushketovite, euhedral magnetite with concentric and/or oscillatory zoning textures, and cauliflower magnetite. Lesser amounts of chalcopyrite and pyrite accompany the iron oxides. Among all these products, mushketovite is dominant and is distributed throughout the deposit. Meanwhile, euhedral magnetite appears in limited amounts at relatively shallow levels in the deposit. By contrast, cauliflower magnetite appears locally in the deeper parts of the deposit, and is associated with green‐colored garnet and calcite. Sulfide minerals are ubiquitously associated with these iron oxides. The oxygen isotope (δ¹⁸O) values of all types of magnetite, quartz, and epidote were found to be ?5.9 to ?2.8‰, 10.5 to 14.9‰, and 3.6 to 6.6‰, respectively. The δ¹⁸O values of quartz–magnetite pairs suggest an equilibrium isotopic temperature near 300°C. The calculated values of δ¹⁸O for the water responsible for magnetite ranged from 2 to 10‰. All the data obtained in this study suggest that the iron oxide deposit at the Chandmani Uul is a typical iron oxide–copper–gold deposit, and that this deposit was formed at an intermediate depth with potassic and sericite–chlorite alteration zones under the oxidized conditions of a hematite‐stable environment. The δ¹⁸O range estimated implies that the ore‐forming fluid was supplied by a crystallizing granodioritic magma exsolving fluids at depth with a significant contribution of meteoric water.     

洱海沉积物粒度记录与气候干湿变迁

通过对洱海现代沉积物的精细采样,将放射性核素精确计年与沉积物粒度研究相结合,重建了 6 0 0多年来洱海区域气候的干湿变迁,为恢复百年尺度的气候干湿变化提供了一条新途径。研究结果表明,15世纪是洱海地区最为湿润的一个世纪;洱海区域存在 10 0a、2 0 0a两种时间尺度的气候干湿准周期波动;自 19世纪末以来洱海区域气候整体上向干旱化方向发展,目前正处于干旱期末期,预计气候将由干旱转向湿润。