X-ray absorption and photoelectron spectroscopy investigation of selenite reduction by FeII-bearing minerals

The long-lived radionuclide 79Se is one of the elements of concern for the safe storage of high-level nuclear waste, since clay minerals in engineered barriers and natural aquifer sediments strongly adsorb cationic species, but to lesser extent anions like selenate (SeVIO4(2-)) and selenite (SeIVO3(2-)). Previous investigations have demonstrated, however, that SeIV and SeVI are reduced by surface-associated FeII, thereby forming insoluble Se0 and Fe selenides. Here we show that the mixed FeII/III (hydr)oxides green rust and magnetite, and the FeII sulfide mackinawite reduce selenite rapidly (< 1 day) to FeSe, while the slightly slower reduction by the FeII carbonate siderite produces elemental Se. In the case of mackinawite, both S(-II) and FeII surface atoms are oxidized at a ratio of one to four by producing a defective mackinawite surface. Comparison of these spectroscopic results with thermodynamic equilibrium modeling provides evidence that the nature of reduction end product in these FeII systems is controlled by the concentration of HSe(-); Se0 forms only at lower HSe(-) concentrations related to slower HSeO3(-) reduction kinetics. Even under thermodynamically unstable conditions, the initially formed Se solid phases may remain stable for longer periods since their low solubility prevents the dissolution required for a phase transformation into more stable solids. The reduction by Fe2+-montmorillonite is generally much slower and restricted to a pH range, where selenite is adsorbed (pH < 7), stressing the importance of a heterogeneous, surface-enhanced electron transfer reaction. Although the solids precipitated by the redox reaction are nanocrystalline, their solubility remains below 6.3 x 10(-8) M. No evidence for aqueous metal selenide colloids nor for Se sorption to colloidal phases was found. Since FeII phases like the ones investigated here should be ubiquitous in the near field of nuclear waste disposals as well as in the surrounding aquifers, mobility of the fission product 79Se may be much lower than previously assumed.     

Neuro-muskuläre Wechselwirkungen Ansätze zur biochemisch-genetischen Analyse

The analysis of hereditary neuro-muscular diseases in the mouse and in other vertebrates may contribute to our understanding of the developmental interactions between spinal cord and sceletal muscle. Meaningful biochemical analysis must be preceded by “biological mixing experiments” to demonstrate whether a given mutation is cell-autonomous, and, if so, which cell type caries the primary defect. Techniques are available to carry out the critical experiment in vivo (artificial chimaeras) or in culture.     

Untersuchungen zum ?kotoxikologischen Sch?digungspotenzial und Erosionsrisiko von kontaminierten Sedimenten in staugeregelten Flüssen

Schwebstoffgebundene Schadstoffe werden durch Sedimentation der Wasserphase und damit der Verfügbarkeit für viele aquatischen Organismen entzogen. W?hrend bei durchschnittlichen hydrologischen. Verh?ltnissen die Freisetzung von Schadstoffen aus stabil gelagerten Sedimenten meist weitgehend unterbunden wird, besteht bei Hochwassereignissen die Gefahr einer Remobilisierung von kontaminierten Ablagerungen. In diesem Beitrag wird ein kombiniertes ?kotoxikologisches und hydraulisches Untersuchungssystem zur Untersuchung der ?kotoxikologischen Belastung und des Erosionsrisikos von Sedimenten vorgestellt. Der integrierte Ansatz wurde am staugeregelten Neckar angewendet, um das Sch?digungspotenzial und die Gefahr einer Remobilisierung an Sedimentbohrkernen der Stauhaltung Lauffen sowie an Schwebstoffen zweier extremer Hochwasser zu überprüfen. Für die Bohrkernsegmente unterhalb einer Erosionsdiskordanz konnte eine sprunghafte Zunahme der ?kotoxikologischen Belastung ermittelt werden. Bei Hochwasserereignissen mit einer 5-j?hrlichen Wiederkehrwahrscheinlichkeit (=HQ₅) k?nnen prinzipiell alle Sedimente, auch die st?rker kontaminierten und erosionsresistenteren Altsedimente, remobilisiert werden. W?hrend der Hochwasserereignisse (HQ₁₅ bis HQ₂₀) kam es zu einer deutlichen Erh?hung des cytotoxischen und mutagenen Sch?digungspotenzials der Schwebstoffe im Vergleich zu einem mittleren Hochwasser im Jahre 1995/96 (HQ₁) Dies schien zumindest teilweise auf die Remobilisierung hochkontaminierter Altsedimente zurückzuführen zu sein.     

评价农场尺度上养分和微量元素动态变化的一个系统方法:以(O)jebyn奶牛场的研究为例

通过把全面的农田试验和矿质风化释放养分以及微量元素循环具体研究结合起来,用一个系统分析方法来评价农场尺度上的养分和微量元素可持续性.为了比较有机和常规农业管理方式,在瑞典北部的Ojebyn奶牛场进行了一个包括磷、钾和锌在内的农场尺度上的实例研究.通过结合不同的元素平衡法(农场总体尺度、畜舍尺度和农田尺度)以及进一步把这些方法应用到FARMFLOw模型,我们能够把子系统内质量流和库结合起来并建立子系统之间联系,来进行农场尺度上的预测.研究发现农场内部的元素流动大,而且农场有内部源(锌)和损失项(钾).在Ojebyn奶牛场形成并得到验证的方法是很有前途的,认为可以应用到任何农场.     

The effects of organic environmental chemicals on the growth of the alga Scenedesmus subspicatus: A contribution to environmental biology

The effective concentrations of 15 chemicals, inhibiting the cell growth of the alga $\text{Scenedesmus subspicatus}$ by 10 % and 50 % during 96 hours, have been investigated in a static test under controlled laboratory conditions.     

Compound dependence of the relationship log Kow and log BCFL

Linear relatinships between log bioconcentration factor (BCF) and log K^ow for a variety of compounds have been reported many times in the literature. Analysis of the thermodynamics of the two partition processes has, however, shown that they are not analogous and that linear relationships can be expected to have different slopes for structurally unrelated compounds. In this study a set of literature lipid normalized BCF (BCF_L) values of chlorbenzenes (CBs) for rainbow trout and polycyclic aromatic hydrocarbons (PAHs) forDaphnia was put together with literature K_ow values. The slopes of the regression lines for log BCF_L versus log K_ow for the two groups of compounds proved to differ significantly in a statistical test using analysis of variance (ANOVA). The difference, which is of significance for estimates of BCFs in environmental modelling of these types of compounds, is explained by the differences in chemical structure of the two groups of compounds.     

Quecksilbergasfeinreinigung mittels metall- und salzpartikelbelegter Trägermaterialien (G/S-Reaktor) Ökotoxizität von Quecksilber und seiner Verbindungen

Waste and process gases from thermal power and metallurgical plants or such products from alkali-chloride industries contain metallic, inorganic and organic mercury. Widespread processes applied to remove the greatest amount of mercury are absorption and adsorption. Caused by the lowering of the emission limit from 200 to 50 µg/m³ [STP] by national and European legislators, considerable efforts have been made to enhance the efficiency of the main separation units of flue gas cleaning plants by applying the appropriate technological measures. This article is focused on the removal of mercury from waste gases. The state of engineering is described, especially with regard to enhancing the efficiency of separation in the raw gas, in wet, dry and quasi-dry processes as well as in tail-end process units. Specially impregnated ceramic carriers can be used for the selective separation of metallic, inorganic and organic mercury. Amalgamation has been investigated as a possible separation mechanism both experimentally and in theory. Using the ceramic reactor, removal rates for gaseous mercury and its compounds can be achieved which are even lower than 50 µg/m³ [STP]. The technology, the separation mechanisms and the ecological advantages through the use of ceramic reactors are presented in the article as well.