Chemical forms of copper and zinc in the surficial sediments of Borollos Lake, Egypt

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Hydrochemistry of carbonate terrains in alpine glacial settings

Nearly 200 analyses of meltwaters, ice and snow from three alpine glacial sites in carbonate terrain are summarized and discussed in terms of sources of solutes and kinetic controls on the progress of weathering reactions. Most data derive from the Swiss Glacier de Tsanfleuron which is based on Cretaceous and Tertiary pure and impure limestones. Two other sites (Marmolada, Italian Dolomites and the Saskatchewan Glacier, Alberta) are based on a mixed calcitic-dolomitic substrate. Most solutes originate from carbonate dissolution; moreover, where pyrite is present its oxidation supplies significant sulphate and forces more dissolution of carbonate. The ratios Sr²⁺/Ca²⁺ and Mg²⁺/Ca²⁺ are much higher in Tsanfleuron melt-waters than local bedrock, a phenomenon that can be reproduced in the laboratory at small percentages of dissolution. These anomalous ratios are attributed to incongruent dissolution of traces of the metastable carbonates Mg-calcite and aragonite. These phases also provide Na⁺ to solution. K⁺ is argued to originate mainly by ion-exchange on clays with solute Ca²⁺. Quartz and very minor feldspar dissolution are also inferred. Locally enhanced input from atmospheric sources is recognized by high Cl^? and associated Na⁺. The progress of weathering reactions has been evaluated by the trends in the data, computer modelling and some simple laboratory experiments. The most dilute samples show a trend towards removal of CO₂ to low partial pressures (c. 10^?5.5 atmospheres), reflecting initially rapid carbonate dissolution and relatively slow dissolution of gaseous CO₂. Later addition of atmospheric CO₂ or acid from pyrite oxidation allows further carbonate dissolution, but solutions show a wide range of saturations, and CO₂ pressures as high as 10^?2.2 where pyrite oxidation is important. In a carbonate terrain, measurement of electroconductivity (corrected to 25°C) and alkalinity in the field allows the following preliminary deductions (where meq stands for milliequivalents): where S is the minimum meq(Ca²⁺ + Mg²⁺) produced by simple dissolution of carbonate unconnected with pyrite oxidation. As with any proxy method, these deductions do not remove the need for chemical analysis of waters in a given study area.     

我国淡水优质草食性鱼类的营养和能学研究Ⅰ.草鱼、团头鲂、长春鳊的生化成分和能值

于1987年及1988年冬季在长江,珠江,湖北武汉东湖、保安湖、洪湖、武黄湖,安徽太平湖,广东仙溪水库采集了草鱼、团头鲂和长春鳊,共328尾,测定了鱼体生化成分。结果表明:1.在同一水域、同一季节收集三种鱼的系列样品,鱼体的水分、蛋白质、脂肪的含量和能值与鱼体重关系显著,三种鱼体的灰分和无氮浸出物的含量与体重无明显关系;2.不同水域的三种鱼,湖泊鱼体的含脂量、能值、能量与蛋白质的比值均高于江中的同种、同龄体长接近的鱼,水分含量则低于江中的鱼,蛋白质、灰分和无氮浸出物差异不大;3.三种鱼的蛋白质均含有常见的17种氨基酸。     

威海湾表层沉积物地球化学

本文对威海湾表层沉积物中的pH,Eh,s~(2-),N,P,Cu,Pb,Zn,Cd和有机质、石油11个化学要素进行了地球化学特征的研究。指出其分布特征及相关性受沉积环境的制约,同时评价了该湾的污染状况,为该湾的开发、利用、防治等提供了科学依据。     

Modeling fracturing-fluid flowback behavior in hydraulically fractured shale gas under chemical potential dominated conditions

Shale with high clay content has caused instability from hydration during the hydraulic fracturing process. Macro-level migration phenomenon of water molecules is induced by the chemical potential difference between low-salinity fracturing fluid and high-salinity formation brine. This study aims to establish the equation for the chemical potential difference between fracturing fluid and formation brine by theoretical deduction in order to investigate the effect of the aforementioned phenomenon on fracturing flowback. Accordingly, a mathematical model was established for the gas–water two-phase flow which driven by the chemical potential difference. Viscous force, capillarity and chemiosmosis were considered as the driving forces. A numerical simulation of fracturing fluid flowback with or without considering of the effect of chemiosmosis was performed. A simulation analysis of the water saturation and salinity profiles was also conducted. Results show that capillarity and chemiosmosis hinder fracturing fluid flowback in different degrees. As the condition worsens, they inhibit more than 80% of water to flow back out of the formation, forming a permanent water lock. This study contributes to improvement of the theory on shale gas–water two-phase flow, establishment of a flowback model that suitable for shale gas wells, and accurate evaluation of the fracturing treatment.     

Crystallization behavior of Na2SO4–MgSO4 salt mixtures in sandstone and comparison to single salt behavior

We report on the crystallization behavior and the salt weathering potential of Na₂SO₄, MgSO₄ and an equimolar mixture of these salts in natural rock and porous stone. Geochemical modeling of the phase diagram of the ternary Na₂SO₄–MgSO₄–H₂O system was used to determine the equilibrium pathways during wetting (or deliquescence) of incongruently soluble minerals and evaporation of mixed electrolyte solutions. Model calculations include stable and metastable solubilities of the various hydrated states of the single salts and the double salts Na₂Mg(SO₄)₂·4H₂O (bloedite), Na₂Mg(SO₄)₂·5H₂O (konyaite), Na₁₂Mg₇(SO₄)₁₃·15H₂O (loeweite) and Na₆Mg(SO₄)₄ (vanthoffite). In situ Raman spectroscopy was used to study the phase transformations during wetting of pure MgSO₄·H₂O (kieserite) and of the incongruently soluble salts bloedite and konyaite. Dissolution of kieserite leads to high supersaturation resulting in crystallization of higher hydrated phases, i.e. MgSO₄·7H₂O (epsomite) and MgSO₄·6H₂O (hexahydrite). This confirms the high damage potential of magnesium sulfate in salt damage of building materials. The dissolution of the incongruently soluble double salts leads to supersaturation with respect to Na₂SO₄·10H₂O (mirabilite). However, the supersaturation was insufficient for mirabilite nucleation. The damage potential of the two single salts and an equimolar salt mixture was tested in wetting–drying experiments with porous sandstone. While the high damage potential of the single salts is confirmed, it appears that the supersaturation achieved during wetting of the double salts at room temperature is not sufficient to generate high crystallization pressures. In contrast, very high damage potentials of the double salts were found in experiments at low temperature under high salt load.1     

Measuring and adjusting the weathering and hydraulic sorting effects for rigorous provenance analysis of sedimentary rocks: a case study from the Jurassic Ashikita Group,south‐west Japan

The present study examines the provenance of the Jurassic Ashikita Group distributed in south‐west Japan, which is composed of the Idenohana, Kyodomari and Sakamoto Formations. Two geochemical diagrams for provenance analysis were utilized, which incorporate full consideration of compositional modifications resulting from weathering (MFW diagram) and hydraulic sorting processes (SiO₂/Al₂O₃–Na₂O/K₂O diagram). The MFW diagram delineates weathering trends of sedimentary rocks and allows estimation of the original source rock composition by tracing the weathering trends backwards to an unweathered domain. Weathering trends of the Idenohana and Kyodomari Formations extend backward to the domain of intermediate and felsic igneous rocks. In contrast, sediments of the Sakamoto Formation do not fit into a linear weathering trend, indicating that the source rock cannot be approximated to igneous rocks. On the SiO₂/Al₂O₃–Na₂O/K₂O diagram, sediments are organized into compositional trends, in which the range reflects compositional variations induced by the hydraulic sorting effect. On this diagram, sediments derived from the igneous and recycled sedimentary provenances can be distinguished by reading the inclination of the trend. By utilizing this principle, source rocks of the Idenohana and Kyodomari Formations are interpreted as igneous rocks and those of the Sakamoto Formation are interpreted as recycled sedimentary rocks. Therefore, these diagrams concurrently estimate the source rock composition through quantifying and adjusting the weathering and sorting effects, and reveal a systematic transition in the provenance of the Ashikita Group. The Idenohana and Kyodomari Formations were supplied chiefly from an igneous provenance, which shifted from intermediate to felsic compositions in stratigraphic order. Whereas, sediments of the Sakamoto Formation were sourced primarily from a recycled sedimentary provenance.     

Fashion and phases of late Pleistocene aggradation and incision in the Alaknanda River Valley, western Himalaya, India

We study the aggradation and incision of the Alaknanda River Valley during the late Pleistocene and Holocene. The morphostratigraphy in the river valley at Deoprayag shows the active riverbed, a cut terrace, and a fill terrace. The sedimentary fabric of the fill terrace comprises four lithofacies representing 1) riverbed accretion, 2) locally derived debris fan, 3) the deposits of waning floods and 4) palaeoflood records. The sedimentation style, coupled with geochemical analysis and Optically Stimulated Luminescence (OSL) dating, indicate that this terrace formed in a drier climate and the river valley aggraded in two phases during 21–18 ka and 13–9 ka. During these periods, sediment supply was relatively higher. Incision began after 10 ka in response to a strengthened monsoon and aided by increase of the tectonic gradient. The cut terrace formed at ~ 5 ka during a phase of stable climate and tectonic quiescence. The palaeoflood records suggest wetter climate 200–300 yr ago when the floods originated in the upper catchment of the Higher Himalaya and in the relatively drier climate ~ 1.2 ka when locally derived sediments from the Lesser Himalaya dominated flood deposits. Maximum and minimum limits of bedrock incision rate at Deoprayag are 2.3 mm/a and 1.4 mm/a.     

A qualitative Natech damage scale for the impact of floods on selected industrial facilities

There is increasing evidence that natural disasters can trigger technological accidents and damage. These so-called Natech accidents can pose a significant risk to regions that are unprepared for responding to them. The European Commission’s Joint Research Centre has recognised the risk associated with Natech events and has started systematic research into Natechs and their underlying dynamics. This work investigates the risk associated with the flooding of industrial installations through an analysis of past case histories and using expert judgement. The potential impact of three levels of flood severity on selected industrial facilities storing and/or processing (eco-)toxic, flammable or explosive materials is analysed qualitatively and a scale is developed that links the flood intensity to the level of potential damage. Our analysis indicates that natural disasters have the potential for triggering hazmat releases and other types of technological accidents. Hence, natural disasters should be considered as separate accident-triggering events in the planning, design and operating stages of industrial facilities that process or store hazardous substances. Our work revealed a lack of detailed information on the occurrence of Natech events which indicates not necessarily a scarcity of Natechs but rather a lack of standardised reporting and record keeping.