The Labrador Sea is one of the few places in the world ocean, where deep water formation takes place. This water is exported from the Labrador Sea to become part of the southward branch of the meridional overturning circulation. Previous observational work has largely focused on the role of deep convection in the interior of the Labrador Sea. Recent evidence from observations and numerical ocean models specifically indicate that processes near the ocean boundaries might be most relevant for both Eulerian downwelling of waters in the Labrador Sea and the fast export of newly transformed waters. We propose to analyze mooring based observations at the western margin of the Labrador Sea together with high resolution numerical model simulations to understand the role both processes play for the meridional overturning circulation in the subpolar North Atlantic. Specifically, we want to test (i) if (and where) downwelling occurs along the margins of the Labrador Sea, (ii) how downwelling relates to the seasonal evolution of convection and eddy activity, (iii) how fast waters newly transformed near the western margin of the Labrador Sea are exported, and (iv) how the two processes (downwelling, fast export) affect the temporal variability of the Atlantic meridional overturning circulation.
Die erste Antragsphase war auf die Bildungsraten und die Speicherung von anthropogenem Kohlenstoff (Cant) im Antarktischen Zwischenwasser (AAIW) fokussiert. Mit Hilfe von Freon (CFC) Daten konnten wir eine signifikante Reduktion der AAIW Bildungsrate von den 1990ern zu den 2000ern Jahren feststellen. Dies führte zu einer geringeren Steigerung der Cant Speicherung als vom atmosphärischen Cant Anstieg und einem unveränderten Ozean zu erwarten war. Um den Schwierigkeiten mit den Randbedingungen auszuweichen (Pazifisches AAIW strömt über die Drake Passage auch in den Atlantik und weiter in den Indischen Ozean) planen wir nun ein globales Vorgehen um in allen Ozeanen die Bildungsraten und Cant Speicherungen in den Zwischen- Tiefen- und Bodenwassermassen zu berechnen. Darüber hinaus wird der Zeitraum bis 2015 ausgedehnt, und wo immer die Datenlage es zulässt, Pentaden- anstatt Dekadenmittelwerte gebildet. Verwendet wird der aktualisierte GlODAPv2 Datensatz und eigene Daten.Die Berechnungen aus den Beobachtungen werden mit den Ergebnissen eines wirbelauflösenden globalen Ozeanmodells (1/10 Grad) kombiniert. Das POP Modell (Los Alamos Laboratory Parallel Ocean Program) mit eines horizontalen Auflösung von 0.1 Grad und 42 Tiefenstufen wird für die letzten 20 Jahre mit einem realistischen Forcing angetrieben und enthält außerdem die Freone als Tracer. Neben dem Vergleich mit einem klimatologischen Antrieb wird das Modell zur Weiterentwicklung der Tracer-Methode verwendet wir z.B. die Unsicherheit von zu wenig Datenpunkten und der Extrpolationsroutine auf die Bildungsraten / Cant Speicherungen. Ein weiterer wichtiger Punkt wird die Bestimmung der TTDs aus Lagrange Trajektorien und der Vergleich mit TTDs aus Tracermessungen sein, sowie die Untersuchung der Rolle der Wirbel, der Vermischung durch Wirbel und der vertikalen Vermischung.
We consider clay minerals, iron oxides and charcoal as major components controlling the formation of interfaces relevant for sorption of organic chemicals, as they control the assemblage of organic matter and mineral particles. We studied the formation of interfaces in batch incubation experiments with inoculated artificial soils consisting of model compounds (clay minerals, iron oxide, char) and natural soil samples. Results show a relevant contribution of both iron oxides and clay minerals to the formation of organic matter as sorptive interfaces for hydrophobic compounds. Thus, we intend to focus our work in the second phase on the characterization of the interface as formed by organic matter associated with clay minerals and iron oxides. The interfaces will be characterized by the BET-N2 and ethylene glycol monoethyl ether (EGME) methods and 129Xe and 13C NMR spectroscopy for determination of specific surface area, sorptive domains in the organic matter and microporosity. A major step forward is expected by the analysis of the composition of the interface at different resolution by reflected-light microscopy (mm scale), SEM (scanning electron microscopy, micrometer scale) and secondary ion mass spectrometry at the nanometer scale (nanoSIMS). The outcomes obtained in combination with findings from cooperation partners will help to unravel the contribution of different types of soil components on the formation and characteristics of the biogeochemical interfaces and their effect on organic chemical sorption.
Perennial fodder cropping potentially increases subsoil biopore density by formation of extensive root systems and temporary soil rest. We will quantify root length density, earthworm abundance and biopore size classes after Medicago sativa, Cichorium intybus and Festuca arundinacea grown for 1, 2 and 3 years respectively in the applied research unit's Central Field Trial (CeFiT) which is established and maintained by our working group. Shoot parameters including transpiration, gas exchange and chlorophyll fluorescence will frequently be recorded. Precrop effects on oilseed rape and cereals will be quantified with regard to crop yield, nutrient transfer and H2-release. The soil associated with biopores (i.e. the driloshpere) is generally rich in nutrients as compared to the bulk soil and is therefore supposed to be a potential hot spot for nutrient acquisition. However, contact areas between roots and the pore wall have been reported to be low. It is still unclear to which extent the nutrients present in the drilosphere are used and which potential relevance subsoil biopores may have for the nutrient supply of crops. We will use a flexible videoscope to determine the root-soil contact in biopores. Nitrogen input into the drilosphere by earthworms and potential re-uptake of nitrogen from the drilosphere by subsequent crops with different rooting systems (oilseed rape vs. cereals) will be quantified using 15N as a tracer.
Existing models of soil organic matter (SOM) formation consider plant material as the main source of SOM. Recent results from nuclear magnetic resonance analyses of SOM and from own incubation studies, however, show that microbial residues also contribute to a large extent to SOM formation. Scanning electron microscopy showed that the soil mineral sur-faces are covered by numerous small patchy fragments (100 - 500 nm) deriving from microbial cell wall residues. We will study the formation and fate of these patchy fragments as continuously produced interfaces in artificial soil systems (quartz, montmorillonite, iron oxides, bacteria and carbon sources). We will quantify the relative contributions of different types of soil organisms to patchy fragment formation and elucidate the effect of redox con-ditions and iron mineralogy on the formation and turnover of patchy fragments. The develop-ment of patchy fragments during pedogenesis will be followed by studying soil samples from a chronosequence in the forefield of the retreating Damma glacier. We will characterize chemical and physical properties of the patchy fragments by nanothermal analysis and microscale condensation experiments in an environmental scanning electron microscope. The results will help understanding the processes at and characteristics of biogeochemical interfaces.
During microbial turnover of organic chemicals in soil, non-extractable residues (NER) are formed frequently. Studies on NER formation usually performed with radioisotope labelled tracer compounds are limited to localisation and quantitative analyses but their chemical composition is left unknown. Recently, we could show for 2,4-dichlorophenoxyacetic acid and ibuprofen that during microbial turnover in soil nearly all NER were derived from microbial biomass, since degrading bacteria use the pollutant carbon for their biomass synthesis. Their cell debris is subsequently stabilised within soil organic matter (SOM) forming biogenic NER (bioNER). It is still unknown whether bioNER are also formed during biodegradation of other, structurally different compound classes of organic contaminants. Therefore, agricultural soil will be incubated with labelled compounds of five classes of commonly used and emerging pesticides: organophosphate, phenylurea, triazinone, benzothiadiazine and aryloxyphenoxypropionic acid. The fate of the label will be monitored in both living and non-living SOM pools and the formation of bioNER will be quantified for each compound over extended periods of time. In addition, soil samples from long-term lysimeter studies with 14C-labelled pesticide residues (e.g. triazine, benzothiazole and phenoxypropionic acid group) will be also analysed for bioNER formation. The results will be summarised to identify the metabolic conditions of microorganisms needed for bioNER formation and to develop an extended concept of risk assessment including bioNER formation in soils.
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.
Organotin and especially butyltin compounds are used for a variety of applications, e.g. as biocides, stabilizers, catalysts and intermediates in chemical syntheses. Tributyltin (TBT) compounds exhibit the greatest toxicity of all organotins and have even been characterized as one of the most toxic groups of xenobiotics ever produced and deliberately introduced into the environment. TBT is not only used as an active biocidal compound in antifouling paints, which are designed to prevent marine and freshwater biota from settlement on ship hulls, harbour and offshore installations, but also as a biocide in wood preservatives, textiles, dispersion paints and agricultural pesticides. Additionally, it occurs as a by-product of mono- (MBT) and dibutyltin (DBT) compounds, which are used as UV stabilizer in many plastics and for other applications. Triphenyltin (TPT) compounds are also used as the active biocide in antifouling paints outside Europe and furthermore as an agricultural fungicide since the early 1960s to combat a range of fungal diseases in various crops, particularly potato blight, leaf spot and powdery mildew on sugar beet, peanuts and celery, other fungi on hop, brown rust on beans, grey moulds on onions, rice blast and coffee leaf rust. Although the use of TBT and TPT was regulated in many countries world-wide from restrictions for certain applications to a total ban, these compounds are still present in the environment. In the early 1970s the impact of TBT on nontarget organisms became apparent. Among the broad variety of malformations caused by TBT in aquatic animals, molluscs have been found to be an extremely sensitive group of invertebrates and no other pathological condition produced by TBT at relative low concentrations rivals that of the imposex phenomenon in prosobranch gastropods speaking in terms of sensitivity. TBT induces imposex in marine prosobranchs at concentrations as low as 0,5 ng TBT-Sn/L. Since 1993, for the littorinid snail Littorina littorea a second virilisation phenomenon, termed intersex, is known. In female specimens affected by intersex the pallial oviduct is transformed of towards a male morphology with a final supplanting of female organs by the corresponding male formations. Imposex and intersex are morphological alterations caused by a chronic exposure to ultra-trace concentrations of TBT. A biological effect monitoring offers the possibility to determine the degree of contamination with organotin compounds in the aquatic environment and especially in coastal waters without using any expensive analytical methods. Furthermore, the biological effect monitoring allows an assessment of the existing TBT pollution on the basis of biological effects. Such results are normally more relevant for the ecosystem than pure analytical data. usw.
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.
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