九龙江-河口表层水体营养盐含量的时空变化及潜在富营养化评价

分别于2012年9月、2013年1、6月,对九龙江两大支流北溪、西溪及河口区开展了3个航次的营养盐监测.研究结果表明,河口区表层水体溶解无机氮（DIN）、总磷（TP）和活性磷酸盐（PO4-P）质量浓度范围分别为0.13-17.35、0.14-1.00和0.00-0.38 mg/dm3,受上游输入和海水稀释作用,营养盐浓度由淡水端至海水端逐渐降低.北溪表层水体的DIN、TP和活性磷酸盐质量浓度范围分别为1.99-24.92、0.12-1.47和0.04-0.68 mg/dm3,受龙岩地区工农业生产及城市进程影响,由上游至下游逐渐降低.西溪表层水体的DIN、TP和活性磷酸盐质量浓度范围分别为2.74-20.61、0.14-0.92和0.02-0.37 mg/dm3,受上游农业生产和下游漳州地区人类活动影响,上下游的DIN质量浓度较高.此外,九龙江沿岸的人类活动可能影响了该地区水体中的溶解无机氮形态组成：北溪和西溪上游的NH4-N和NO3-N占比分别较高.水期分析表明,2013年1月的DIN浓度显著高于其他水期,而不同区域TP和活性磷酸盐的水期波动不尽相同.营养盐结构分析表明,九龙江总体处于磷限制状态,但在河口及北溪部分站位,CDIN/CPO4-P比值已达到适合浮游生物生长繁殖的水平.潜在富营养化程度评价表明,九龙江河口多数站位均处于N或P限制的富营养化级别,但由于N、P营养盐的绝对浓度较高,具有水华暴发的潜在风险.     

哈萨克斯坦萨亚克铜矿田代表性矿区矽卡岩矿物的组成及其意义研究

哈萨克斯坦萨亚克铜矿田产于晚石炭世闪长玢岩、石英闪长玢岩或花岗闪长玢岩与中石炭统灰岩的接触带上,铜矿体呈透镜状、脉状产于矽卡岩中。其成矿期可以划分为4个阶段：石榴子石矽卡岩阶段（Ⅰ）、绿帘石-石榴子石矽卡岩阶段（Ⅱ）、磁铁矿阶段（Ⅲ）和石英-硫化物阶段（Ⅳ）。铜矿化主要发生在石英-硫化物阶段,形成石英、黄铁矿、黄铜矿、磁黄铁矿,呈浸染状或脉状产于不同类型的矽卡岩或块状磁铁矿中。矽卡岩中的石榴子石有3种类型：石榴子石矽卡岩中的钙铁榴石（Grt-a）、交代钙铁榴石的含Al钙铁榴石（Grt-b）和绿帘石-石榴子石矽卡岩中具有环带结构的石榴子石（Grt-c）。从第一类到第三类石榴子石,平均w（Al₂O₃）从<1%逐渐升高至~5%;分子式中平均Fe³⁺原子数从2.15逐渐降低至1.57,显示成矿体系中Al的摩尔浓度逐渐升高、氧逸度逐渐降低。绿帘石-石榴子石矽卡岩中发育少量辉石,属于钙铁辉石-透辉石系列,在辉石分类图中落于普通辉石范围内。矽卡岩的地质特征、矿物组合和矿物化学特征表明,萨亚克矽卡岩是与花岗岩类侵入岩有关的岩浆热液与灰岩通过接触交代反应形成的钙质矽卡岩,随着矽卡岩化和成矿作用的进行,成矿体系的温度和氧逸度逐渐降低、pH值升高,导致磁铁矿和黄铁矿-磁黄铁矿-黄铜矿矿物组合依次发生沉淀。     

Arsenic Distribution Pattern in Different Sources of Drinking Water and their Geological Background in Guanzhong Basin,Shaanxi, China

To study arsenic(As) content and distribution patterns as well as the genesis of different kinds of water, especially the different sources of drinking water in Guanzhong Basin, Shaanxi province, China, 139 water samples were collected at 62 sampling points from wells of different depths, from hot springs, and rivers. The As content of these samples was measured by the intermittent flowhydride generation atomic fluorescence spectrometry method(HG-AFS). The As concentrations in the drinking water in Guanzhong Basin vary greatly(0.00–68.08 μg/L), and the As concentration of groundwater in southern Guanzhong Basin is different from that in the northern Guanzhong Basin. Even within the same location in southern Guanzhong Basin, the As concentrations at different depths vary greatly. As concentration of groundwater from the shallow wells(50 m deep, 0.56–3.87 μg/L) is much lower than from deep wells(110–360 m deep, 19.34–62.91 μg/L), whereas As concentration in water of any depth in northern Guanzhong Basin is 10 μg/L. Southern Guanzhong Basin is a newly discovered high-As groundwater area in China. The high-As groundwater is mainly distributed in areas between the Qinling Mountains and Weihe River; it has only been found at depths ranging from 110 to 360 m in confined aquifers, which store water in the Lishi and Wucheng Loess(Lower and Middle Pleistocene) in the southern Guanzhong Basin. As concentration of hot spring water is 6.47–11.94 μg/L; that of geothermal water between 1000 and 1500 m deep is 43.68–68.08 μg/L. The high-As well water at depths from 110 to 360 m in southern Guanzhong Basin has a very low fluorine(F) value, which is generally 0.10 mg/L. Otherwise, the hot springs of Lintong and Tangyu and the geothermal water in southern Guanzhong Basin have very high F values(8.07–14.96 mg/L). The results indicate that highAs groundwater in depths from 110 to 360 m is unlikely to have a direct relationship with the geothermal water in the same area. As concentration of all reservoirs and rivers(both contaminated and uncontaminated) in the Guanzhong Basin is 10 μg/L. This shows that pollution in the surface water is not the source of the high-As in the southern Guanzhong Basin. The partition boundaries of the high- and low-As groundwater area corresponds to the partition boundaries of the tectonic units in the Guanzhong Basin. This probably indicates that the high-As groundwater areas can be correlated to their geological underpinning and structural framework. In southern Guanzhong Basin, the main sources of drinking water for villages and small towns today are wells between 110–360 m deep. All of their As contents exceed the limit of the Chinese National Standard and the International Standard(10 μg/L) and so local residents should use other sources of clean water that are 50 m deep, instead of deep groundwater(110 to 360 m) for their drinking water supply.     

Studies on the Thermodynamics and Thermal Chemistry Properties for Lithium Salts and Their Aqueous Solution Systems

正1 Introduction With the industrial development of lithium battery,nuclear and aerospace industry,the demands of metal lithium and its compounds are increasing significantly.Lithium is called as the energy of the metal in the new century(Zhang et al.2001).The total reserve of lithium resources around the world7     

The role of lithology,catchment size and the alluvial zone on the hydrogeochemistry of two intermittent Mediterranean streams

Hydrology and solute concentrations of two intermittent Mediterranean streams draining two nested catchments were compared. The two catchments were mainly underlain by granitic rocks and different types of sericitic schists. Only the lowland catchment had an alluvial zone and a well‐developed riparian forest. The rainfall–runoff relationship and the correlation between daily flow concentrations showed that hydrological behaviour was similar at both sites during most of the year. However, reverse fluxes were detected during the wetting and drying up periods only in the stream with an alluvial zone. The intermittence in stream flow also had effects on absolute solute concentrations, temporal solute dynamics and streamwater stoichiometry. Streamwater chemistry was not affected by drainage area, except for cations produced mainly by bedrock dissolution (i.e. calcium and magnesium) that increased with increasing catchment size. Differences in the relationship among cations and anions were detected between the two streams, which could be attributed to biogeochemical processes occurring in the alluvial zone. The multivariate model used in this study showed that stoichiometry was more useful than absolute concentrations when analyzing the influence of different lithologies on streamwater chemistry. Such differences were amplified in autumn, likely due to a low hydrological connectivity between the two nested catchments. Copyright © 2007 John Wiley & Sons, Ltd.     

Hydrogeochemical balance of forest umbrisol profiles (‘Sierra de Gata’, central western Spain)

Three techniques for obtaining soil water solutions (gravitational and matrical waters extracted using both in situ tension lysimeters and in vitro pressure chambers) and their later chemical analysis were performed in order to know the evolution of the soil‐solution composition when water moves down through the soil, from the Ah soil horizon to the BwC‐ or C‐horizons of forest soils located in western Spain. Additionally, ion concentrations and water volumes of input waters to soil (canopy washout) and exported waters (drainage solutions from C‐horizons) were determined to establish the net balance of solutes in order to determine the rates of leaching or retention of ions. A generalized process of sorption or retention of most components (even Cl^?) was observed, from the soil surface to the C‐horizon, in both gravitational and matrical waters, with H₄SiO₄, Mn²⁺, Na⁺, and SO₄^2? being the net exported components from the soil through the groundwater. These results enhance the role of the recycling effect in these forest soils. The net percentages of elements retained in these forest soils, considering the inputs and the outputs balance, were 68% K⁺, 85% Ca²⁺, 58% Mg²⁺, 7% Al³⁺, 5% Fe³⁺, 34% Zn²⁺, 57% Cl^?, and 20% NO₃^?, and about 75% of dissolved organic carbon was mineralized. Copyright © 2007 John Wiley & Sons, Ltd.     

Late Quaternary tephra layers around Raoul and Macauley Islands,Kermadec Arc: implications for volcanic sources,explosive volcanism and tephrochronology

A suite of deep‐sea cores were collected along transects up to 100 km across the fore‐arc and back‐arc regions of the predominantly submarine Kermadec arc near Raoul and Macauley islands, southwest Pacific. The cores reveal a macroscopic tephra record extending back >50 ka. This is a significant addition to the dated record of volcanism, previously restricted to fragmented late Holocene records exposed on the two islands. The 27 macroscopic tephra layers display a wide compositional diversity in glass (～50–78 wt% SiO₂). Many tephra layers comprise silicic shards with a subordinate mafic shard population. This could arise from magma mingling and may reflect mafic triggering of the silicic eruptions. Broadly, the glass compositions can be distinguished on diverging high‐K and low‐K trends, most likely arising from different source volcanoes. This distinction is also reflected in the tephra records exposed on Raoul (low‐K) and Macauley (high‐K) islands, the likely source areas. Heterogeneous tephra comprising shards of both high‐ and low‐K affinity, silicic and mafic compositions, and more homogeneous tephra with subordinate outlier shard compositions, are best explained by post‐depositional mixing of separate eruption deposits or contemporaneous eruptions. Evidently, the slow sedimentation rates of the calcareous oozes (～10¹–10² mm ka^?1) were insufficient to adequately separate and preserve closely spaced eruption deposits. This exemplifies the difficulty in assessing eruption frequencies and magmatic trends, and erecting a tephrostratigraphy, using geochemical fingerprinting in such environments. Despite these difficulties, the ca. 5.7 ka Sandy Bay Tephra erupted from Macauley Island can be correlated over a distance of >100 km, extending east and west of the island, showing that the mostly submerged volcanoes are capable of wide tephra dispersal. Hence there is potential for developing chronostratigraphies for the southwest Pacific beyond the region covered by the extensive rhyolite marker beds from the Taupo Volcanic Zone. Copyright © 2011 John Wiley & Sons, Ltd.     

Chemical composition and leaching characteristics of granules made of wood ash and dolomite

 In 1995, the central heating plant Draken in Kalmar, Sweden, started manufacturing a granular ash product for nutrient recycling to forest soil, instead of dumping the ash in landfills. Chemical composition, leaching and dissolution characteristics were determined for the Draken wood ash, the dolomite used in granule manufacturing and the final granule product. The heavy metal concentrations in fly ash were within the limit values recommended by the Swedish National Board of Forestry for ash recycling, except for Cd and As levels which occasionally exceeded the limit values. The Ca, Mn and P levels were too low for nutrient recycling at the time. Adding dolomite insures that the levels of the important nutrients Ca and Mg are sufficient in the granules. After 7 months in the field, about 60 % of Na and K was leached out from granules. Between 20 and 60% of trace elements Mo, Sc, V, Y and Zr were leached out after 7 months. The release of Ca and Mg was low, 1–5% during 7 months. Received: 12 July 1999 · Accepted: 31 August 1999     

NUMERICAL MODELING OF CUMULUS CLOUD CHEMISTRY—PART Ⅰ.MODEL DEVELOPMENT

A one-dimensional cumulus cloud chemistry model(1CCCM)is developed to simulate cloudphysical processes and chemical processes during the evolution of a convective cloud.The cloudphysical submodel includes a detailed microphysical parameterized scheme of 20 processes.Thechemistry submodel is composed of three parts:gas phase chemistry,aqueous phase chemistry andscavenging of soluble gases.The gas phase reaction mechanism contains 85 reactions among 45species including 13 organics.The aqueous phase reaction mechanism contains 54 reactions among40 species and 12 ion equilibria.Mass of 19 gases is transported between the gas phase and theaqueous phase.With this model,studies may be made to analyze the interactions among processesduring lifetime of a cumulus cloud.     

The effect of terrace geology on ground‐water movement and on the interaction of ground water and surface water on a mountainside near Mirror Lake,New Hampshire,USA

The west watershed of Mirror Lake in the White Mountains of New Hampshire contains several terraces that are at different altitudes and have different geologic compositions. The lowest terrace (FSE) has 5 m of sand overlying 9 m of till. The two next successively higher terraces (FS2 and FS1) consist entirely of sand and have maximum thicknesses of about 7 m. A fourth, and highest, terrace (FS3) lies in the north‐west watershed directly adjacent to the west watershed. This highest terrace has 2 m of sand overlying 8 m of till. All terraces overlie fractured crystalline bedrock. Numerical models of hypothetical settings simulating ground‐water flow in a mountainside indicated that the presence of a terrace can cause local ground‐water flow cells to develop, and that the flow patterns differ based on the geologic composition of the terrace. For example, more ground water moves from the bedrock to the glacial deposits beneath terraces consisting completely of sand than beneath terraces that have sand underlain by till. Field data from Mirror Lake watersheds corroborate the numerical experiments. The geology of the terraces also affects how the stream draining the west watershed interacts with ground water. The stream turns part way down the mountainside and passes between the two sand terraces, essentially transecting the movement of ground water down the valley side. Transects of water‐table wells were installed across the stream's riparian zone above, between, and below the sand terraces. Head data from these wells indicated that the stream gains ground water on both sides above and below the sand terraces. However, where it flows between the sand terraces the stream gains ground water on its uphill side and loses water on its downhill side. Biogeochemical processes in the riparian zone of the flow‐through reach have resulted in anoxic ground water beneath the lower sand terrace. Results of this study indicate that it is useful to understand patterns of ground‐water flow in order to fully understand the flow and chemical characteristics of both ground water and surface water in mountainous terrain. Copyright © 2007 John Wiley & Sons, Ltd.