Due to the often practised uncontrolled disposal into the environment, olive oil production wastewater (OPWW) is presently a serious environmental problem in Palestine and Israel. The objectives of this interdisciplinary trilateral research project are (i) to understand the mechanisms of influence of the olive oil production wastewater on soil wettability, water storage, interaction with organic agrochemicals and pollutants; (ii) monitor short-term and long-term effects of OPWW land application in model laboratory and field experiments; (iii) identify the components responsible for unwanted changes in soil properties and (iv) analyse the mechanisms of association of OPWW OM with soil, the interplay between climatic conditions, pH, presence of multivalent cations and the resulting effects of land application. Laboratory incubation experiments, field experiments and new experiments to study heat-induced water repellency will be conducted to identify responsible OPWW compounds and mechanisms of interaction. Samples from field experiments and laboratory experiments are investigated using 3D excitation-emission fluorescence spectroscopy, thermogravimetry-differential thermal analysis-mass spectrometry (TGA-DSC-MS), LC-MS and GC-MS analyses. We will combine thermal decomposition profiles from OPWW and OPWW-treated soils in dependence of the incubation status using TGA-DSC-MS, contact angle measurements, sorption isotherms and the newly developed time dependent sessile drop method (TISED). The resulting process understanding will open a perspective for OPWW wastewater reuse in small-scale and family-scale olive oil production busi-nesses in the Mediterranean area and will further help to comprehend the until now not fully un-ravelled effects of wastewater irrigation on soil water repellency.
We are currently facing the urgent need to improve our understanding of carbon cycling in subsoils, because the organic carbon pool below 30 cm depth is considerably larger than that in the topsoil and a substantial part of the subsoil C pool appears to be much less recalcitrant than expected over the last decades. Therefore, small changes in environmental conditions could change not only carbon cycling in topsoils, but also in subsoils. While organic matter stabilization mechanisms and factors controlling its turnover are well understood in topsoils, the underlying mechanisms are not valid in subsoils due to depth dependent differences regarding (1) amounts and composition of C-pools and C-inputs, (2) aeration, moisture and temperature regimes, (3) relevance of specific soil organic carbon (SOC) stabilisation mechanisms and (4) spatial heterogeneity of physico-chemical and biological parameters. Due to very low C concentrations and high spatio-temporal variability of properties and processes, the investigation of subsoil phenomena and processes poses major methodological, instrumental and analytical challenges. This project will face these challenges with a transdisciplinary team of soil scientists applying innovative approaches and considering the magnitude, chemical and isotopic composition and 14C-content of all relevant C-flux components and C-fractions. Taking also the spatial and temporal variability into account, will allow us to understand the four-dimensional changes of C-cycling in this environment. The nine closely interlinked subprojects coordinated by the central project will combine field C-flux measurements with detailed analyses of subsoil properties and in-situ experiments at a central field site on a sandy soil near Hannover. The field measurements are supplemented by laboratory studies for the determination of factors controlling C stabilization and C turnover. Ultimately, the results generated by the subprojects and the data synthesized in the coordinating project will greatly enhance our knowledge and conceptual understanding of the processes and controlling factors of subsoil carbon turnover as a prerequisite for numerical modelling of C-dynamics in subsoils.
Ziel des Projektes ist eine Bestandsaufnahme der Wassermassenverteilung und der Zirkulation im Arktischen Ozean. Stabile Sauerstoffisotopen (delta18O) des Wassers ist ein konservativer Tracer und werden zusammen mit hydrochemischen Daten dazu verwendet das vom Schelf stammende Süßwasser (Flusswasser und Meereis-Schmelze oder Bildung) und die aus dem Pazifik stammende Komponente zu untersuchen. Auf diese Weise wird der Einfluss dieser Wassermassen in der arktischen Salzgehaltsschichtung (Halokline), dem Atlantischen Zwischenwasser und dem Tiefen- und Bodenwasser des Arktischen Ozeans quantifiziert werden. Es ist bekannt, dass die Verteilung der Pazifischen Komponente starken Veränderungen auf dekadischen Zeitskalen unterliegt aber auch in den Süßwasserverteilungen im Transpolaren Drift Strom wurden 2007 starke Variationen beobachtet welche somit auf zusätzliche jährliche Variationen hinweisen. Es ist nicht bekannt ob die 2007 beobachteten Variationen ein permanentes Phänomen sind und ob diese mit dem weitgehenden Fehlen des Pazifischen Wassers in diesem Zeitraum zusammenhängen. Die geplante flächendeckende und quantitative Erfassung der Süßwasserverteilung und des Pazifischen Wassers werden daher dazu beitragen, den Einfluss und die möglichen Rückkopplungsmechanismen der arktischen Hydrographie auf den arktischen und globalen Klimawandel weitergehend zu verstehen.
Water is an intrinsic component of ecosystems acting as a key agent of lateral transport for particulate and dissolved nutrients, forcing energy transfers, triggering erosion, and driving biodiversity patterns. Given the drastic impact of land use and climate change on any of these components and the vulnerability of Ecuadorian ecosystems with regard to this global change, indicators are required that not merely describe the structural condition of ecosystems, but rather capture the functional relations and processes. This project aims at investigating a set of such functional indicators from the fields of hydrology and biogeochemistry. In particular we will investigate (1) flow regime and timing, (2) nutrient cycling and flux rates, and (3) sediment fluxes as likely indicators. For assessing flow regime and timing we will concentrate on studying stable water isotopes to estimate mean transit time distributions that are likely to be impacted by changes in rainfall patterns and land use. Hysteresis loops of nitrate concentrations and calculated flux rates will be used as functional indicators for nutrient fluxes, most likely to be altered by changes in temperature as well as by land use and management. Finally, sediment fluxes will be measured to indicate surface runoff contribution to total discharge, mainly influenced by intensity of rainfall as well as land use. Monitoring of (1) will be based on intensive sampling campaigns of stable water isotopes in stream water and precipitation, while for (2) and (3) we plan to install automatic, high temporal-resolution field analytical instruments. Based on the data obtained by this intensive, bust cost effective monitoring, we will develop the functional indicators. This also provides a solid database for process-based model development. Models that are able to simulate these indicators are needed to enable projections into the future and to investigate the resilience of Ecuadorian landscape to global change. For the intended model set up we will couple the Catchment Modeling Framework, the biogeochemical LandscapeDNDC model and semi-empirical models for aquatic diversity. Global change scenarios will then be analyzed to capture the likely reaction of functional indicators. Finally, we will contribute to the written guidelines for developing a comprehensive monitoring program for biodiversity and ecosystem functions. Right from the beginning we will cooperate with four SENESCYT companion projects and three local non-university partners to ensure that the developed monitoring program will be appreciated by locals and stakeholders. Monitoring and modelling will focus on all three research areas in the Páramo (Cajas National Park), the dry forest (Reserva Laipuna) and the tropical montane cloud forest (Reserva Biologica San Francisco).
Der Oberflächenfilm (SML) ist die oberste dünne Schicht des Ozeans und Teil jeglicher Wechselwirkung zwischen Luft und Meer, wie Gasaustausch, atmosphärische Deposition und Aerosolemission. Die Anreicherung von organischer Materie (OM) in der SML modifiziert die Luft-Meer-Austauschprozesse, aber welche OM-Komponenten selektiv angereichert werden, sowie warum und wann sie dies tun, ist weitgehend unbekannt (Engel et al., 2017). Unsere bisherige Forschung hat gezeigt, dass Biopolymere aus photoautotropher Produktion wichtige Komponenten der SML sind und den Luft-Meer-Austausch beeinflussen, indem sie als Biotenside (Galgani et al., 2016; Engel et al., 2018) und als Quelle primärer organischer Aerosole (Trueblood et al., 2021) wirken. Die Motivation unseres Projektes ist es daher, die dynamischen Anreicherungsprozesse von OM in der SML aufzuklären und zu beschreiben, wobei ein besonderer Schwerpunkt auf der Auflösung der OM-Quellen liegt. Mit unserem Modellierungsansatz ist es das Ziel, unser mechanistisches Verständnis der Zusammenhänge zwischen den Wachstumsbedingungen des Planktons, der Produktion und der Freisetzung von Biomolekülen, einschließlich potentieller Tenside, und der Akkumulation von OM in der SML zu konsolidieren. Eine solche Modellentwicklung wird in hohem Maße von den Ergebnissen und Erkenntnissen der verschiedenen Teilprojekte des BASS-Konsortiums profitieren. Umgekehrt ist es unsere Motivation, ein Modell zu etablieren, das als Synthesewerkzeug für die Interpretation und Integration von Feld-, Mesokosmen- und Labormessungen der OM-Anreicherung in der SML anwendbar wird.Relevanz für die Forschungsgruppe BASS - SP1.1 wird die Quellen, die Menge und die biochemische Zusammensetzung von OM in der SML entschlüsseln und damit wichtige Informationen für alle BASS-Teilprojekte liefern. Der primäre Ursprung von OM im Oberflächenozean ist die photosynthetische Produktion und die wichtigsten biochemischen Komponenten von frisch produzierter OM, d.h. Kohlenhydrate, Aminosäuren und Lipide, unterliegen der mikrobiellen Verarbeitung (SP1.2) und Photoreaktionen innerhalb der SML (SP1.3, SP1.4) und füllen auch den Pool der gelösten organischen Substanz (DOM) auf (SP1.5). Die Modellentwicklung in SP1.1 stellt eine Verbindung zwischen der Produktion von OM und ihrer Anreicherung innerhalb der SML her und zielt darauf ab, die entsprechenden Auswirkungen auf den Luft-Meer-Gasaustausch (SP2.1) zu bestimmen, indem Änderungen des Impulsflusses auf den Ozeanoberflächenschichten (SP2.2) sowie des Auftriebs (SP2.3) berücksichtigt werden. Das vorgeschlagene SML-Submodell wird auf der Grundlage der Ergebnisse aus SP1.4 und SP2.3 verfeinert. Ergebnisse aus den Modellsensitivitätsanalysen werden ergänzende Informationen über oberflächenaktive Eigenschaften verschiedener OM Komponenten und deren Auswirkungen auf Luft-Meer-Austauschprozesse liefern, die innerhalb von BASS ausgewertet werden.
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.
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'.
Ziel: The objective of our project is to investigate the impact of different natural and anthropogenic environmental and climatic parameters (CO2, ozone, UV-B, drought, nanoparticles, soil and airborne pollutants) on the potentiality for increases of allergenic components in Ragweed pollen. Methode: Acquisition of the complete transcriptome/proteome under constant and the different climatic parameters listed above will be carried out. In addition secondary metabolite analyses and electron microscopy will be performed. In addition secondary metabolite analyses and electron microscopy will be performed.
Bestandteile in Ensembles. Unterschutzstellung als Teil von Mehrheiten unbeweglicher Sachen, die aufgrund eines übergeordneten Bezugs Kulturdenkmäler sind, ohne dass jeder einzelne Bestandteil die Voraussetzungen des Satzes 1 erfüllen muss (Ensembles), wie Orts-, und Platzgefüge, Siedlungen oder Straßenzüge (§ 2 Absatz 2 Nr. 2 DSchG).