水声学方法对黄河口水下底坡失稳现象研究

对黄河三角洲东北部地区的高分辨率水声学资料进行了综合研究。根据所记录的破坏土体变形程度、运动产生的平面形状和地貌特征形态,对土体失稳过程进行分类：浅表土体变形、塌陷凹坑、滑坡和沉积物重力流。结果表明：（１）浅表土体形变的变形程度最低,出现在研究区斜坡上部平滑海底,主要为绳网状泄水构造和表层拉张裂隙。（２）塌陷凹坑在研究区内广泛出现,是局部土体液化后发生了垂直沉降的结果。（３）滑坡多发生在水下斜坡的中上部,由弧形塌陷区、狭窄的冲沟通道和负地形沉积物堆积区组成。滑坡陡坎后缘发现拉张裂隙。（４）沉积物重力流是土体发生变形程度最大,搬运距离最长的土体破坏变形形式。局部区域多次受到沉积物重力流切割和充填作用。     

Spheroidal weathering of granite porphyry with well‐developed columnar joints by oxidation,iron precipitation,and rindlet exfoliation

Spheroidal weathering, one of the important rock weathering styles, has been attributed to chemical weathering by the water from joint surfaces, and mechanical aspects of the weathering have not been well addressed. We made an investigation on spheroidal weathering of Miocene granite porphyry with well‐developed columnar joints and found that this spheroidal weathering proceeds through chemical processes and accompanying mechanical processes. The investigation of the textures, physical properties, mineralogy, and chemistry of the porphyry revealed the presence of a brown band on the surface margins of corestones, representing the oxidation of pyrite and chlorite, and the precipitation of iron hydroxides, and the consequent generation of micro‐cracks within the band. During weathering, oxidation progresses inwards from joints that surround the rindlets, including both high‐angle columnar and low‐angle planar joints, and causes rounding of the unweathered interior portion of the rock. Microscopic observations of the brown band embedded with fluorescent resin show that pores are first filled with iron hydroxides, and that micro‐cracks then form parallel to the oxidation front in the outer portion of the brown band. Iron hydroxide precipitation increases the P‐wave velocity in the brown band, while micro‐crack formation decreases the tensile strength of the rock. Where the brown band has thickened to ~6 cm, the micro‐cracks are connected to one another to create continuous cracks, which separate the rindlets from the corestone. Micro‐crack formation parallel to the corestone surface may be attributed to compressive stresses generated by small amounts of volumetric expansion due to the precipitation of iron hydroxides in the brown band. Earth surface is under oxidizing environments so that precipitation of iron hydroxides commonly occurs; the spheroidal weathering in this paper is a typical example of the combination of chemical and mechanical processes under such environments. Copyright © 2016 John Wiley & Sons, Ltd.     

海水浓度对生物接触氧化法处理废水的影响

研究了海水浓度对生物接触氧化法处理废水的影响。结果表明,在淡水中添加海水超过35％时,生物接触氧化法去除废水的化学耗氧量(COD)的效果随着海水浓度的增加而降低．添加海水10％～25％时,COD的去除效果好,25％时COD最高总去除率可达87．8％．处理效果几乎与纯淡水的对照组(COD总去除率88．6％)等同。     

西藏多龙矿集区铜金流体演化过程探讨 ——来自硫同位素的证据

西藏多龙矿集区发育世界典型的斑岩铜矿系统,文章选取区内多个代表性矿床开展硫同位素研究,并结合前人数据,为探讨该成矿系统成矿物质来源、流体演化过程提供了新证据.研究表明,波龙、拿若、拿厅、拿顿和铁格隆南矿床δ34S平均值相似(接近于0),指示含矿岩浆提供了各矿床所需的硫元素.此外,区内典型矿床流体演化过程可分为2类:①流体演化主要受控于温度变化,表现为δ34S随温度降低而降低(如拿顿矿床);②流体演化受温度和氧化还原状态共同影响,表现为δ34S随温度降低而升高(如:波龙和拿若矿床),或是随温度降低,δ34S波动变化范围较大(如拿厅和铁格隆南矿床).结合岩相学证据,文章推测热液体系氧化还原状态的变化是由水岩反应所导致,最后,文章提出多龙矿集区内矿化阶段硫化物通常具有较低的δ34S,指示成矿流体为高氧化性流体,并且该特征在类似矿床的找矿勘查工作中也可发挥积极的指示作用.     

The influence of light intensity,SO2, NOx and C3H6 on sulfate aerosol formation

The photochemical oxidation of SO₂ in the presence of NO and C₃H₆ was studied in a 18.2 liter pyrex reactor. When light intensity, irradiation time and SO₂ concentration were constant, SO₄ ^2- concentration, derived from the total volume of aerosol produced, peaked when [C₃H₆]/[NO] was approximately 6.0. Another increase im SO₄ ^2- formation was reached at very high ratios (>50). The experimental observations are consistent with the two SO₂ oxidation mechanisms. At low [C₃H₆]/[NO] ratios, the processes proceed via the HO–SO₂ reaction, while at high ratios the O₃–C₃H₆ adduct is assumed to oxidize SO₂ to produce SO₄ ^2- aerosols.     

内陆水体好氧甲烷氧化过程研究进展

内陆水体是全球碳循环的关键组成部分,是大气中甲烷(CH_4)的重要来源,每年从内陆淡水与自然湿地排放进入大气的CH4约为185～357 Tg/a.通常,内陆水体中CH_4主要由分布于水层底部的厌氧区或沉积层内的产甲烷菌介导产生,其向水层表面传输的过程中易被甲烷氧化菌所氧化.甲烷氧化菌可分为好氧甲烷氧化菌和厌氧甲烷氧化菌,有氧条件下,由好氧甲烷氧化菌介导的好氧甲烷氧化过程是水体中甲烷氧化过程的主要形式,湖泊底部产生的CH_4总量中约有99%可以被上覆水体中的好氧甲烷氧化过程所消耗.本文收集文献综合分析阐明,好氧甲烷氧化过程是由水环境因子、水文条件以及不同内陆水体的生态系统特征共同调控,同时也表现在了好氧甲烷氧化菌的生境偏好上.复杂的调控过程构建了内陆水体向大气输送CH_4的动态平衡,并最终反映在内陆水体对全球CH_4循环、碳循环作出的贡献上.     

Methane Oxidation in the Water Column of Xiangxi Bay,Three Gorges Reservoir

Four field campaigns are carried out to quantify the methane (CH₄) oxidation rate in Xiangxi Bay (XXB) of the Three Gorges Reservoir (TGR), China. The water depth of the sampling site varied from 13 to 30 m resulting from the water level fluctuation of the TGR. The CH₄ oxidation rates are measured in situ as the decline of dissolved CH₄ concentration versus time in incubated, and those rates. The CH₄ oxidation rates range from 1.18 × 10^?3 to 3.69 × 10^?3 µmol L^?1 h^?1, with higher values and stronger variation during summer. A static floating chamber method is used to measure CH₄ emitted to the atmosphere resulting in an annual mean flux of 4.79 µmol m^?2 h^?1. The CH₄ emission rate is significantly negatively correlated with the water level. The results show that a large fraction of CH₄ is consumed in the water column with a range of 28.97–55.90 µmol m^?2 h^?1, accounting for ≈69–98% of the total CH₄ input into the water column, and more than 90% is consumed outside the summer, when the water level is lowest. Water depth, which is dominated by water level of the TGR, is a potentially important driver for CH₄ oxidation and atmospheric emission in the tributary bay.     

Peroxymonosulfate Improves the Activity and Stability of Manganese Oxide for Oxidation of Arsenite to Arsenate

Manganese oxide has been widely investigated for oxidation of arsenite (As(III)) to arsenate (As(V)) due to its high redox potential; however, it becomes extremely unstable after reuse. Here, As(III) oxidation activity and stability of manganese oxide in the presence of peroxymonosulfate (PMS) is investigated. Batch experimental results reveal that manganese oxide/PMS exhibits high catalytic activity for As(III) oxidation compared to manganese oxide or PMS alone. Addition of PMS to manganese oxide not only reveals long‐term stability for As(III) oxidation, but also shows high As(III) oxidation activity in the presence of coexisting ions such as As(V) and phosphate. Quenching tests reveal that As(III) oxidation in the manganese oxide/PMS system is attributed to activation of PMS by manganese oxide at different oxidation states (Mn(III) and Mn(IV)), and the generation of sulfate radicals that are responsible for As(III) oxidation.