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'Umweltschutz im Tischlerhandwerk'

Linking soil architecture formation with changing permafrost regime to carbon turnover in high latitude soils at multiple spatial scales

Most soils develop distinct soil architecture during pedogenesis and soil organic carbon (SOC) is sequestered within a hierarchical system of mineral-organic associations and aggregates. Permafrost soils store large amounts of carbon due to their permanently frozen subsoil and a lack of oxygen in the active layer, but they lack complex soil structure. With permafrost thaw more oxidative conditions and increasing soil temperature presumably enhance the build-up of more complex units of soil architecture and may counterbalance, at least partly, SOC mineralization. We aim to explore the development of mineral-organic associations and aggregates under different permafrost impact with respect to SOC stabilization. This information will be linked to environmental control factors relevant for SOC turnover at the pedon and stand scale to bridge processes occurring at the aggregate scale to larger spatial dimensions. We will combine in situ spectroscopic techniques with fractionation approaches and identify mechanisms relevant for SOC turnover at different scales by multivariate statistics and variogram analyses. From this we expect a deeper knowledge about soil architecture formation in the transition of permafrost soils to terrestrial soils and a scale-spanning mechanistic understanding of SOC cycling in permafrost regions.

Formation of mega-glendonites in the aftermath of the Paleocene-Eocene thermal maximum

Glendonites are pseudomorphs after the mineral ikaite (CaCO3 x 6H2O) and composed of calcite (CaCO3). In the past, they have been used as a paleo-thermometer because the primary mineral ikaite, according to observations and experiments, seems to be formed at temperatures near freezing, high alkalinity and high phosphate concentrations in marine sediments. An enigmatic occurrence of the largest glendonites known world-wide, in the Early Eocene Fur Formation of northwestern Denmark offers the unique possibility to shed more light on the actual mechanism and controlling parameters of ikaite formation. Right in the aftermath of the Paleocene-Eocene thermal maximum, a time known for its global pertubation in the global carbon cycle, the formation of authigenic calcium carbonate concretions start in the Fur Formation. In a specific stratigraphic interval inbetween these concretions, the glendonites can be found. We will investigate if termperature changes or changes in geochemical parameters of the Danish Basin caused the sudden formation of ikaite during a time interval that was based on known paleoclimatic reconstructions (semi tropic) not favorable for ikaite formation.

Vorbereitung der Aktion 'Globale Umweltpartnerschaft - Aufruf zu einem Oekologischen Marshallplan'

Aufbau der 'Oekologischen Station Borna/Birkenhain

Einfluss von Ionen auf das atmosphärische Partikelwachstum - Studien an einem Flussreaktor und einer Aerosolkammer

Sekundäre Partikelneubildung ist eine Hauptquelle für atmosphärische Partikel mit wichtigen Folgen für das Klima und die menschliche Gesundheit. Dieses Vorhaben untersucht die Rolle von Luft Ionen bei der sekundären Partikelneubildung in Flussreaktor- und Aerosolkammer-Experimenten unter kontrollierten Laborbedingungen. Trotz beträchtlicher Fortschritte in der Messtechnik zur Untersuchung der atmosphärischen Nukleation und des Partikelwachstums bestehen weiterhin Verständnislücken hinsichtlich der grundlegenden physikalischen und chemischen Prozesse. Insbesondere die möglichen Effekte von Ionen-Partikel-Wechselwirkungen und von Ionenchemie auf die Partikelneubildung werden kontrovers diskutiert. In Ergänzung zu bestehenden Forschungsprogrammen hinsichtlich der Rolle von Ionen im initialen Nukleationsschritt wird vorgeschlagen, Ionen-Partikel-Wechselwirkungen während des anschließenden Partikelwachstums zu untersuchen und sich dabei auf direkte Messungen des Ladungszustands, der Wachstumsraten und der chemischen Zusammensetzung von sekundärem organischem Aerosol zu konzentrieren. Hierzu werden der Ladungszustand und die Wachstumsraten von Partikelpopulationen mit einem modifizierten Mobilitätspartikelspektrometer unter wohldefinierten Randbedingungen in Laborexperimenten quantifiziert. In einem nächsten Schritt werden die neuartigen Messmöglichkeiten unseres Aerosol-Massenspektrometers CAChUP voll ausgeschöpft, um den Beitrag verschiedener organischer Vorläufergase zur chemischen Zusammensetzung von sekundärem organischen Aerosol bei variierenden Ladungszuständen zu quantifizieren. Schließlich werden die Ergebnisse dieser Experimente durch Messungen zur sekundären organischen Partikelbildung bei wohldefinierten Ionenkonzentrationen an einer Aerosolkammer überprüft. Die vorgeschlagene Forschungsagenda ist somit darauf abgestimmt, mögliche ladungs-katalysierte chemische Mechanismen bei der sekundären Aerosolbildung besser einzuordnen.

Biogeochemical reactivity of Fe-organic matter coprecipitates

Iron(III) (hydr)oxide-organic associations in soils have been recognized to play an important role in the biogeochemical cycling of iron, carbon, and of nutrients like phosphate. In temporarily moist or water-logged soils such associations can form via the coprecipitation of dissolved organic matter (OM) with Fe(III) (hydr)oxides (FHOs). At present, it is generally unknown which factors control the formation and composition of Fe(III)-OM coprecipitates and how the structural properties translate into the cycling of the FHO and OM component involved. The objectives of the project are thus to elucidate (i) the structural properties of Fe(III)- OM coprecipitates under different environmental conditions, (ii) the subsequent stability of Fe(III)-OM coprecipitates against dissolution under both oxic as well as anoxic conditions, (iii) the changes in Fe(III)-OM coprecipitate composition upon redox oscillations, and (iii) their cumulative effects on oxyanion sorption. To achieve these goals, various batch experiments will be conducted. By using multiple analytical tools, this project will gain a fundamental understanding of the abiotic and biotic controls on the formation, structure, and biogeochemical reactivity of Fe(III)-OM coprecipitates in acidic and neutral temporarily moist soils and soils subject to redox oscillations.

Effect of diffusive/dispersive processes on stable isotope ratios of organic contaminants in aquifer systems

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.

Schulen Landkreis Lüneburg

Im Landkreis Lüneburg gibt es ein flächendeckendes Angebot an allgemeinbildenden Schulen. Dazu gehören die Grundschulen, Hauptschulen, Realschulen, Gymnasien, Gesamtschulen und Förderschulen. Je nach Schulform unterscheiden sich die Zugangsvoraussetzungen, pädagogischen Konzepte und Abschlüsse. Die Daten zeigen die Standorte der Schulen des Landkreises nach Schulform.

Kindertageseinrichtungen Landkreis Lüneburg

Standorte verschiedener Kindertageseinrichtungen im Landkreis Lüneburg

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