The effect of acid deposition on base cation cycling in a karstic-forested catchment： Evidence from strontium isotopes

Bedrock weathering and atmospheric deposition are the two primary sources of base cations （K^＋, Na^＋, Ca^2＋ and Mg^2＋） to forest ecosystems. Therefore, the key problem is to understand the relative inputs from these two sources and the cycling in the ecosystem. This study focuses on the effects of acid deposition on cation cycling in a small-forested karstic catchment in Guizhou Province. Sr isotope ratios were used as a tracer for understanding the transport process between the different cation pools： rock, soil, surface water, atmospheric deposition and plant. The samples of wet deposition, total deposition, throughfall, surface and ground waters, vegetation, and soil were monthly collected. The exchangeable Sr^2＋ and Ca^2＋ in soil samples were extracted by using 1 M ammonium acetate. The leaf-tissue samples were ashed at 550℃, and the residue was digested in ultrapure HClO4 and HNO3. All water samples were filtrated through 0.45 μm aperture filter paper. Base cation concentrations and Sr isotopic composition were analyzed for all the samples. The results show that acid deposition （average pH 4.9） frequently occurred in the studied region. Cation abundance follows an increasing manner from rainwater, throughfall, to surface water or ground water samples, suggesting that acid deposition at first eiuviates Ca^2＋ , Mg^2＋ and Sr^2＋ from leaf, then the exchangeable cations from soil, and at last cations accumulate in surface water or ground water.     

High resolution profiles of trace metals in pore waters of marine and riverine sediments assessed by DET and DGT

In polluted aquatic systems, toxic metals are often accumulated in bottom sediments. They are, however, not necessarily stored definitively because diagenetic processs can modify redox, pH and even the amount of complexing ligands, releasing the trace metals back into the pore waters and the water column. Especially the labile metal fraction in the pore waters is important since this is the bioavailable fraction determining the bio-toxicity of the sediments. The goal of our study was therefore to assess, with novel sampling techniques, this bioavailable metal fraction in the pore waters as well as the flux towards the overlying water column. High-resolution profiles of trace metals in pore waters of marine and riverine sediments were assessed by DET （diffusive equilibrium in thin films） and DGT （diffusive gradients in thin films） gel techniques. The DET technique uses a diffusive gel layer that equilibrates with the aquatic system and with this technique the concentrations of total dissolved trace metals are obtained directly. The DGT technique uses an acrylamide diffusive gel backed by a resin gel （Chelex） which binds trace metals. With the DGT technique only labile species of selected metals can be captured. According to the redox potential measurements, the marine sediments were suboxic （200 mV to -220 mV versus Ag/AgCl electrode）, while the riverine sediments were completely anoxic （-160 mV to -220 mV versus Ag/AgCl electrode）. This redox potential was apparently controlling the trace metals species in the pore waters： for example a strong correlation between Mn and Co was found in the riverine sediments （for DET and DGT sampling）, while in the marine sediments trace metals presented various behaviors.     

Microwave-assisted extraction of organochlorine pesticides from sediments and determination by gas chromatograph with electron capture detection

A simple and rapid procedure to extract organochlorine pesticides （OCPs） from sediments by means of microwave energy is proposed. Sediment samples were irradiated with microwaves in a closed vessel system while immersed in hexane-acetone （1 ： 1, v/v）. The sample extracts were cleaned up using solid phase extraction with Florisil as adsorbent. Pesticides were eluted with hexane-ethyl acetate （80 ： 20, v/v） and determined by gas chromatographic separation with electron capture detection. Three oven programs were assayed with two different solvent mixtures in order to achieve adequate experimental conditions for the complete extraction of organochlorine pesticides from the matrix. Different variables such as the composition of extraction solvent,     

浙江古代青瓷(1127～1279年)的化学组成及其意义

本文用ENGLE-型微探针能量色散X荧光光谱(EDXRF)技术测定了一批青釉瓷残片中的16种元素氧化物的含量,其残片来自浙江杭州地区的南宋郊坛窑和老虎洞窑。由主量元素判别方程的Q值表明,两类青釉瓷均属官窑制品。主成分统计分析看出,郊坛官窑与老虎洞官窑的瓷釉成分有明显不同,但其胎质成分的分布,却有部分的重叠,这显示了当时两处官窑的工匠们在使用胎料中的交往。从釉层、过渡层、和胎层的Al2O3和CaO的含量数据表明,郊坛官窑和老虎洞官窑的青釉瓷制品,分别存有厚度为120～140μm和230～240μm的过渡层,表明两处使用釉料和烧制工艺上的…     

浙江景宁大源山火山岩地貌景观及开发远景

浙江景宁大源山是一处尚待开发的地质旅游景区,由晚侏罗世陆相火山岩组成,火山作用强烈,岩石类型齐全,火山机构发育典型。火山岩地貌景观独特,以峰柱、峰丛、造型石为特色,融畲族风情和生态景观于一体,具有很高科学品位及研究价值,兼具观光游览、科普休闲等多项功能,具备建立地质公园的科学基础,具有很好的开发前景。     

旧供水井化学处理方法介绍--以加德满都市旧供水井修复为例

本文以加德满都市旧供水井修复项目为例,针对因滤水管缝隙被化学物质堵塞,导致井出水量逐年减少的旧供水井。通过井下电视摄像系统检查,采用六偏磷酸钠、氨基黄酸等有机酸,结合刷洗、高压喷射等机械方法进行处理,使旧供水井出水量得到明显提高。     

西藏俄卡地银多金属异常区地球化学

异常形态、分布严格受推覆断裂控制,范围大、浓集中心明显,浓度变化及因子载荷表明。区内找Ag、Pb有利,而Sb又为其最佳指示元素。     

类脂化合物单体碳稳定同位素在古气候环境研究中的意义

类脂化合物极大地扩展了全球变化研究的深度，尤其是单体碳稳定同位素技术在古气候、古环境重建上有着重要作用。基于近些年来国内外的最新研究成果，就类脂化合物单体碳同位素在古气候环境方面的应用研究进行了较为全面的评述。已有研究表明利用类脂化合物单体碳同位素组成可以追溯到海洋和湖泊环境中陆源有机质的物源，其母源区历史时期 C3、C4植被的变迁以及区域性的古气候、古环境重建。     

珠峰高程的雪面高和岩石高

2005年珠峰高程测量，精确测定了珠穆朗玛峰峰项的雪面高和岩石高。     

欧北-大湾地区火山岩储层成因机制的研究

从分布、成分组成、形成机制等几个方面探讨了辽河油田东部凹陷中段最主要的火山岩储层－－粗面岩的成因机制，并对其成为该区良好储层的原因进行了探讨，通过对比说明了另一类火山岩－－玄武岩不含油的原因，并建立了成因模式，最后得出结论：粗面岩呈喷发状态产出，由于其硅质含量高，流动性小，容易在构造高部位形成巨厚的火山岩锥或火山岩钏，从而造成其大部分在水上，结晶较好且储层物性极佳，同时因其裂缝发育，这些因素结合起来使其成为良好的会层。从供油方式来看，其成藏方式属于侧生式，而从生储盖组合方式来看，其属于自生、自储、自盖式成藏组合。同时给出了其成藏模式。