Forschungsschwerpunkt: - Entwicklung differenzierter Materialien und E-Learning-Konzeptionen zur Qualifizierung von Zielgruppen, die in energiebezogenen Bereichen tätig sind bzw. entsprechende Qualifikationen anstreben - systematische mediendidaktische Fortentwicklung bestehender Blended-Learning-Konzeptionen. Ziele: - Vermittlung grundlegende energiewirtschaftliche Zusammenhänge für Nicht-Ökonomen, die in der Energiebranche tätig sind bzw. entsprechende Qualifikationen anstreben - Ziel ist das Erlangen vertiefter Einsichten in die verschiedenen Facetten der Energieversorgung und -nutzung, um ein breiteres Verständnis für die vielschichtigen Aufgaben und Anforderungen an Unternehmen in der Branche. Beschreibung: - Im Rahmen der ersten Projektphase wurde ein internetgestützter Qualifizierungsbaustein 'Energy Economics' entwickelt und eine internetgestützte Lehreinheit konzipiert. Diese wurde im Wintersemester 2013/2014 im Studiengang 'Engineering Physics' erprobt und evaluiert. Das Feedback der Teilnehmer fiel sehr positiv aus. - In der zweiten Projektphase (2014) ein weiterer internetgestützter Qualifizierungsbaustein entwickelt, auf dessen Basis ebenfalls eine Veranstaltung konzipiert, durchgeführt und evaluiert wird. Im Mittelpunkt steht darin die Auseinandersetzung mit den erneuerbaren Energien, insbesondere im Hinblick auf ihren Einsatz in Entwicklungs- und Schwellenländern. Die Lehrveranstaltung wird ausschließlich onlinebasiert durchgeführt werden. Ergebnisse/Materialien: Qualifizierungsbaustein 'Energy Economics', der sich thematisch mit den Schwerpunkten - grundlegende Strukturen internationaler Energiemärkte (insb. Erdöl, Erdgas, Kohle), - Besonderheiten der Märkte für leitungsgebundene Energieversorgung, - Bedeutung energiepolitischer Rahmensetzung auf den Märkten sowie - Förderung erneuerbarer Energien und ihrer Wirkung auf Märkten auseinandersetzt.
Chlorinated ethylenes are prevalent groundwater contaminants. Numerous studies have addressed the mechanism of their reductive dehalogenation during biodegradation and reaction with zero-valent iron. However, despite insight with purified enzymes and well-characterized chemical model systems, conclusive evidence has been missing that the same mechanisms do indeed prevail in real-world transformations. While dual kinetic isotope effect measurements can provide such lines of evidence, until now this approach has not been possible for chlorinated ethylenes because an adequate method for continuous flow compound specific chlorine isotope analysis has been missing. This study attempts to close this prevalent research gap by a combination of two complementary approaches. (1) A novel analytical method to measure isotope effects for carbon and chlorine. (2) A carefully chosen set of well-defined model reactants representing distinct dehalogenation mechanisms believed to be important in real-world systems. Isotope trends observed in biotic and abiotic environmental dehalogenation will be compared to these model reactions, and the respective mechanistic hypotheses will be confirmed or discarded. With this hypothesis-driven approach it is our goal to elucidate for the first timdehalogenation reactions.
For surface soils, the mechanisms controlling soil organic C turnover have been thoroughly investigated. The database on subsoil C dynamics, however, is scarce, although greater than 50 percent of SOC stocks are stored in deeper soil horizons. The transfer of results obtained from surface soil studies to deeper soil horizons is limited, because soil organic matter (SOM) in deeper soil layers is exposed to contrasting environmental conditions (e.g. more constant temperature and moisture regime, higher CO2 and lower O2 concentrations, increasing N and P limitation to C mineralization with soil depth) and differs in composition compared to SOM of the surface layer, which in turn entails differences in its decomposition. For a quantitative analysis of subsoil SOC dynamics, it is necessary to trace the origins of the soil organic compounds and the pathways of their transformations. Since SOM is composed of various C pools which turn over on different time scales, from hours to millennia, bulk measurements do not reflect the response of specific pools to both transient and long-term change and may significantly underestimate CO2 fluxes. More detailed information can be gained from the fractionation of subsoil SOM into different functional pools in combination with the use of stable and radioactive isotopes. Additionally, soil-respired CO2 isotopic signatures can be used to understand the role of environmental factors on the rate of SOM decomposition and the magnitude and source of CO2 fluxes. The aims of this study are to (i) determine CO2 production and subsoil C mineralization in situ, (ii) investigate the vertical distribution and origin of CO2 in the soil profile using 14CO2 and 13CO2 analyses in the Grinderwald, and to (iii) determine the effect of environmental controls (temperature, oxygen) on subsoil C turnover. We hypothesize that in-situ CO2 production in subsoils is mainly controlled by root distribution and activity and that CO2 produced in deeper soil depth derives to a large part from the mineralization of fresh root derived C inputs. Further, we hypothesize that a large part of the subsoil C is potentially degradable, but is mineralized slower compared with the surface soil due to possible temperature or oxygen limitation.
Das Jena Experiment hat es sich zum Ziel gesetzt Zusammenhänge zwischen Pflanzendiversität und Ökosystemprozessen zu untersuchen. Unsere Arbeiten beschäftigen sich mit einer der Schlüsselgruppen in unterirdischen Ökosystemprozessen - den Pilzen. Das Wirtsspektrum arbuskulärer Mykorrhizapilze (AMF) wird innerhalb der Monokultur-Plots untersucht. In Polykulturen unterschiedlicher Diversität soll der Zusammenhang zwischen Artenreichtum von Pflanzen und AMF vertiefend studiert werden. Durch ein Experiment mit stabilen Isotopen soll der Beitrag der AMF für die Nährstoffverteilung zwischen einzelnen Pflanzenarten, aber auch zwischen funktionellen Gruppen näher beleuchtet werden. Weiterhin wird untersucht, ob Zusammenhänge zwischen Stickstoffmineralisierung, Anreicherung organischer Substanzen sowie der Diversität und dem Expressionsprofil pilzlicher Laccasegene bestehen.
Terrestrial green algae and cyanobacteria are typical and abundant components of biological soil crusts in the Polar Regions. These communities form water-stable aggregates that have important ecological roles in primary production, nitrogen fixation, nutrient cycling, water retention and stabilization of soils. Although available data on green algae and cyanobacteria are generally very limited for the Arctic and Antarctica, their functional importance as ecosystem developers in nutrient poor environments is regarded as high. Therefore, the main goal of the interdisciplinary project is, for the first time, a precise evaluation of their 1.) Biodiversity as well as of 2.) The infra-specific genetic diversity, 3.) ecophysiological performance and 4.) transcriptomics of the most abundant taxa in biological soil crusts isolated from the Antarctic Peninsula and Arctic Svalbard. Biodiversity will be investigated using a classical culture approach in combination with molecular-taxonomical methods as well as with metagenomics. The infra-specific genetic diversity of the most abundant green algae and cyanobacteria will be studied using fingerprinting techniques, and a range of selected populations characterized in relation to their physiological plasticity. Temperature and water availability, two key environmental factors for terrestrial organisms, are currently changing in Polar Regions due to global warming, and hence their effect on growth and photosynthesis response patterns will be comparatively investigated. The data will indicate whether and how global change influence population structure and ecological performance of key organisms in polar soil crusts, and help to make predictions on the future significance of the ecological functions of these pioneer communities. Such a multiphasic approach has never been applied before to soil algae and cyanobacteria in both Polar Regions, and hence represents one of the key innovations of this proposal.
Magnetic properties of ferrimagnetic minerals depend on their crystal lattice, anisotropy, chemical composition and grain size. The latter parameter is strongly controlled by microstructures, which are significant for the interpretation of the magnetic properties of shocked magnetic minerals. Fracturing and lattice defects are the main causes for magnetic domain size reduction and generate an increase in coercivity and the suppression of magnetic transitions (e.g. 34 K transition in pyrrhotite, Verwey transition in magnetite).Especially for an adequate investigation of shock-induced modifications in ferromagnetic minerals, a combination of microstructural and magnetic measurements is therefore essential.This project focusses on two significant aspects of extreme conditions - the consequence of shock waves on natural material on Earth and on the magnetic mineralogy of exotic magnetic minerals in iron meteorites. In order to obtain general correlations between deformation structures and magnetic properties, the specific magnetic properties and carriers as well as microstructures of samples from two impact structures in marine targets (Lockne and Chesapeake Bay) will be compared with shocked magnetite ore and magnetite-bearing target lithologies from outside the crater (Lockne) as well as from undeformed megablocks within the crater (Chesapeake Bay). We will test the hypothesis if shock-related microstructures and associated magnetic properties can significantly be overprinted by postshock hydrothermal alteration. We especially want to focus on the Verwey transition (TV) as lower TVs are described for shocked impact lithologies. Hence, the main focus of this study lies on magneto-mineralogical investigations which combine low- and high-temperature magnetic susceptibility and saturation isothermal remanent magnetization with mineralogical and microstructural investigations. The same methods will then be used for the investigation of iron meteorites, whose magnetic properties are often controled by exotic magnetic minerals like cohenite, schreibersite and daubreelite in addition to the metal phases. Magnetic transition temperatures of those phases are poorly documented in relation to their chemical composition as well as to their crystallographic and microstructural configuration. For a general understanding of shock-related magnetization processes in extraterrestrial and terrestrial material, however, it is crucial to obtain a general correlation between the initial 'unshocked' state and the subsequent shock- and alteration-related overprints.
The relevance of biogeochemical gradients for turnover of organic matter and contaminants is yet poorly understood. This study aims at the identification and quantification of the interaction of different redox processes along gradients. The interaction of iron-, and sulfate reduction and methanogenesis will be studied in controlled batch and column experiments. Factors constraining the accessibility and the energy yield from the use of these electron acceptors will be evaluated, such as passivation of iron oxides, re-oxidation of hydrogen sulfide on iron oxides. The impact of these constraints on the competitiveness of the particular process will then be described. Special focus will be put on the evolution of methanogenic conditions in systems formerly characterized by iron and sulfate reducing condition. As methanogenic conditions mostly evolve from micro-niches, methods to study the existence, evolution and stability of such micro-niches will be established. To this end, a combination of Gibbs free energy calculations, isotope fractionation and tracer measurements, and mass balances of metabolic intermediates (small pool sizes) and end products (large pool sizes) will be used. Measurements of these parameters on different scales using microelectrodes (mm scale), micro sampling devices for solutes and gases (cm scale) and mass flow balancing (column/reactor scale) will be compared to characterize unit volumes for organic matter degradation pathways and electron flow. Of particular interest will be the impact of redox active humic substances on the competitiveness of involved terminal electron accepting processes, either acting as electron shuttles or directly providing electron accepting capacity. This will be studied using fluorescence spectroscopy and parallel factor analysis (PARAFAC) of the gained spectra. We expect that the results will provide a basis for improving reactive transport models of anaerobic processes in aquifers and sediments.
Water, carbon and nitrogen are key elements in all ecosystem turnover processes and they are related to a variety of environmental problems, including eutrophication, greenhouse gas emissions or carbon sequestration. An in-depth knowledge of the interaction of water, carbon and nitrogen on the landscape scale is required to improve land use and management while at the same time mitigating environmental impact. This is even more important under the light of future climate and land use changes.In the frame of the proposal 'Uncertainty of predicted hydro-biogeochemical fluxes and trace gas emissions on the landscape scale under climate and land use change' we advocate the development of fully coupled, process-oriented models that explicitly simulate the dynamic interaction of water, carbon and nitrogen turnover processes on the landscape scale. We will use the Catchment Modelling Framework CMF, a modular toolbox to implement and test hypothesis of hydrologic behaviour and couple this to the biogeochemical LandscapeDNDC model, a process-based dynamic model for the simulation of greenhouse gas emissions from soils and their associated turnover processes.Due to the intrinsic complexity of the models in use, the predictive uncertainty of the coupled models is unknown. This predictive (global) uncertainty is composed of stochastic and structural components. Stochastic uncertainty results from errors in parameter estimation, poorly known initial states of the model, mismatching boundary conditions or inaccuracies in model input and validation data. Structural uncertainty is related to the flawed or simplified description of natural processes in a model.The objective of this proposal is therefore to quantify the global uncertainty of the coupled hydro-biogeochemical models and investigate the uncertainty chain from parameter uncertainty over forcing data uncertainty up the structural model uncertainty be setting up different combinations of CMF and LandscapeDNDC. A comprehensive work program has been developed structured in 4 work packages, that consist of (1) model set up, calibration and uncertainty assessment on site scale followed by (2) an application and uncertainty assessment of the coupled model structures on regional scale, (3) global change scenario analyses and finally (4) evaluating model results in an ensemble fashion.Last but not least, a further motivation of this proposal is to provide project results in a manner that they support planning and decision taking under uncertainty, as this proposal is part of the package proposal on 'Methodologies for dealing with uncertainties in landscape planning and related modelling'.
Groundwater contamination by organic compounds represents a widespread environmental problem. The heterogeneity of geological formations and the complexity of physical and biogeochemical subsurface processes, often hamper a quantitative characterization of contaminated aquifers. Compound specific stable isotope analysis (CSIA) has emerged as a novel approach to investigate contaminant transformation and to relate contaminant sources to downgradient contamination. This method generally assumes that only (bio)chemical transformations are associated with isotope effects. However, recent studies have revealed isotope fractionation of organic contaminants by physical processes, therefore pointing to the need of further research to determine the influence of both transport and reactive processes on the observed overall isotope fractionation. While the effect of gasphase diffusion on isotope ratios has been studied in detail, possible effects of aqueous phase diffusion and dispersion have received little attention so far.The goals of this study are to quantify carbon (13C/12C) and, for chlorinated compounds, chlorine (37Cl/35Cl) isotope fractionation during diffusive/dispersive transport of organic contaminants in groundwater and to determine its consequences for source allocation and assessment of reactive processes using isotopes. The proposed research is based on the combination of high-resolution experimental studies, both at the laboratory (i.e. zero-, one- and two-dimensional systems) and at the field scales, and solute transport modeling. The project combines the expertise in the field of contaminant transport with the expertise on isotope methods in contaminant hydrogeology.
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