Chemische Reaktionen von Chlorvinylarsinverbindungen (Lewisit)

2,2′-Dichlorodivinylarsine chloride (Lewisite II) react by room temperature quickly with alcohols in an equilibrium reaction to yield 2,2′-Dichlorodivinylarsine ether. The reactions are not quantitative. The methyl-, ethyl-and propylether are not stable.     

Exemplifying whole-plant ozone uptake in adult forest trees of contrasting species and site conditions

Whole-tree O3 uptake was exemplified for Picea abies, Fagus sylvatica and Larix decidua in stands at high and low altitude and contrasting water availability through sap flow measurement in tree trunks, intrinsically accounting for drought and boundary layer effects on O3 flux. O3 uptake of evergreen spruce per unit foliage area was enhanced by 100% at high relative to low elevation, whereas deciduous beech and larch showed similar uptake regardless of altitude. The responsiveness of the canopy conductance to water vapor and, as a consequence, O3 uptake to soil moisture and air humidity did not differ between species. Unifying findings at the whole-tree level will promote cause-effect based O3 risk assessment and modeling.     

Passivsammler zur Wasseruntersuchung

The topography and motion of contaminant plumes in groundwater may be determined by surveying the three-dimensional distribution of contaminant freights [1] as well as through a period-integral monitoring by contaminant dosimeters [1]. Conventional methods of taking water samples for chemical analysis cannot fulfill any of these requirements. Sorption active passive collectors suitable for corresponding surveys in gaseous phases are unsuitable for examination in aquifers. Passive collectors for the examination of undisturbed aquifers represent the central part of a probing device system developed by the authors for monitoring chemical and hydraulic parameters within all kinds of aquifers. These passive collectors permit both a determination of the relative contaminant freights at deliberate vertical spacing of vertically ordered measuring points, and period-integrating detection of vertical profiles of relative contaminant freights. The easy-to-handle passive collectors are suitable for the collection of organic and inorganic contaminants and may be evaluated by standardized chemical analysis methods. In this way, passive collectors fulfill the essential prerequisites for purpose-oriented monitoring of contaminant plumes. Moreover, passive collectors for ground water monitoring are well suited for the in situ-examination of any other aquifer, both still and fluent, regardless of its depth or extent. Examples of application may be sewage ducts, sewage plants, rivers, lakes, oceans, water samples and especially the identification of contaminants and trace substances.     

Mixing-controlled biodegradation in a toluene plume--results from two-dimensional laboratory experiments

Various abiotic and biotic processes such as sorption, dilution, and degradation are known to affect the fate of organic contaminants, such as petroleum hydrocarbons in saturated porous media. Reactive transport modeling of such plumes indicates that the biodegradation of organic pollutants is, in many cases, controlled by mixing and therefore occurs locally at the plume's fringes, where electron donors and electron-acceptors mix. Herein, we aim to test whether this hypothesis can be verified by experimental results obtained from aerobic and anaerobic degradation experiments in two-dimensional sediment microcosms. Toluene was selected as a model compound for oxidizable contaminants. The two-dimensional microcosm was filled with quartz sand and operated under controlled flow conditions simulating a contaminant plume in otherwise uncontaminated groundwater. Aerobic degradation of toluene by Pseudomonas putida mt-2 reduced a continuous 8.7 mg L(-1) toluene concentration by 35% over a transport distance of 78 cm in 15.5 h. In comparison, under similar conditions Aromatoleum aromaticum strain EbN1 degraded 98% of the toluene infiltrated using nitrate (68.5+/-6.2 mg L(-1)) as electron acceptor. A major part of the biodegradation activity was located at the plume fringes and the slope of the electron-acceptor gradient was steeper during periods of active biodegradation. The distribution of toluene and the significant overlap of nitrate at the plume's fringe indicate that biokinetic and/or microscale transport processes may constitute additional limiting factors. Experimental data is corroborated with results from a reactive transport model using double Monod kinetics. The outcome of the study shows that in order to simulate degradation in contaminant plumes, detailed data sets are required to test the applicability of models. These will have to deal with the incorporation of existing parameters coding for substrate conversion kinetics and microbial growth.     

Application of microbial hot spots enhances pesticide degradation in soils

Through transfer of an active, isoproturon degrading microbial community, pesticide mineralization could be successfully enhanced in various soils under laboratory and outdoor conditions. The microbes, extracted from a soil having high native ability to mineralize this chemical, were established on expanded clay particles and distributed to various soils in the form of microbial "hot spots". Both, diffusion controlled isoproturon mass flow towards these "hot spots" (6microg d(-1)) as well as microbial ability to mineralize the herbicide (approximately 5microg d(-1)) were identified as the main processes enabling a multiple augmentation of the native isoproturon mineralization even in soils with heavy metal contamination. Soil pH-value appears to exert an important effect on the sustainability of this process.