In June 2010, the DLR Group of Systems Analysis started an investigation about innovative financing of Concentrating Solar Power Plants (CSP) in countries of the Middle East and North Africa. We found a possible strategy for the market introduction of concentrating solar power (CSP) plants in the Middle East and North Africa (MENA) that will not require considerable subsidization and will not constitute a significant burden for electricity consumers in the region. In the first section, the paper explains the need of MENA countries for sustainable supply of electricity and calculates the cost of electricity for a model case country. In the second part, the cost development of concentrating solar power plants is calculated on the basis of expectations for the expansion of CSP on a global level. After that, the challenges for the market introduction of CSP in MENA are explained. Finally, we present a strategy for the market introduction of CSP in MENA, removing the main barriers for financing and starting market introduction in the peak load and the medium load segment of power supply. The paper explains why long-term power purchase agreements (PPA) for CSP should be calculated on the basis of avoided costs, starting in the peak load segment. Such PPA are not yet available, the paper aims to convince policy makers to introduce them. The attached power point file shows some examples of time series of load and supply by CSP in the different load segments and shows the graphs used in the report. The attached Excel Sheet gives the time series of load and supply by CSP for the different load segments for a total reference year.
The proposal addresses the potential of subsoil to contribute to K nutrition of crops. More specifically we will address the processes controlling release of K from interlayer of 2:1 clay minerals as this is expected to be the dominant K fraction in the subsoil. While it has been shown in the past that this so called 'non-exchangeable' K can be released due to root activity, there are controversial results concerning the role of soil solution K concentration in the rhizosphere required to trigger the process. Likewise little information is available about the concentration dynamics of other cations (NH4, Ca) in the rhizosphere and their impact on K release and vermiculitization supposed to be associated with this process. Model studies with substrate from the central field trial will be conducted in compartment systems equipped with micro suction cups. The measurement of dynamic changes of soil solution composition with increasing distance from the root surface will be combined with investigations of changes in mineralogy by XRD, TEM and SEM-EDX. Changes of mineralogy as a result of plant induced K release from interlayer will also be studied on bulk soil and rhizosphere samples collected within the central field and the central microcosm experiment and with mineral bags exposed in the field during a cropping cycle. Finally, X-ray CT will be used to access changes in soil texture, i.e. clay distribution around roots and the temporal spread of roots in biopores which is a prerequisite for K uptake from such structures.
Arsenic-contaminated ground- and drinking water is a global environmental problem with about 1-2Prozent of the world's population being affected. The upper drinking water limit for arsenic (10 Micro g/l) recommended by the WHO is often exceeded, even in industrial nations in Europe and the USA. Chronic intake of arsenic causes severe health problems like skin diseases (e.g. blackfoot disease) and cancer. In addition to drinking water, seafood and rice are the main reservoirs for arsenic uptake. Arsenic is oftentimes of geogenic origin and in the environment it is mainly bound to iron(III) minerals. Iron(III)-reducing bacteria are able to dissolve these iron minerals and therefore release the arsenic to the environment. In turn, iron(II)-oxidizing bacteria have the potential to co-precipitate or sorb arsenic during iron(II)- oxidation at neutral pH followed by iron(III) mineral precipitation. This process may reduce arsenic concentrations in the environment drastically, lowering the potential risk for humans dramatically.The main goal of this study therefore is to quantify, identify and isolate anaerobic and aerobic Fe(II)-oxidizing microorganisms in arsenic-containing paddy soil. The co-precipitation and thus removal of arsenic by iron mineral producing bacteria will be determined in batch and microcosm experiments. Finally the influence of rhizosphere redox status on microbial Fe oxidation and arsenic uptake into rice plants will be evaluated in microcosm experiments. The long-term goal of this research is to better understand arsenic-co-precipitation and thus arsenic-immobilization by iron(II)-oxidizing bacteria in rice paddy soil. Potentially these results can lead to an improvement of living conditions in affected countries, e.g. in China or Bangladesh.
Zur Lösung von Fluss- und reaktiven Transportgleichungen in heterogenen Grundwassersystemen werden neue Global Random Walk (GRW) Algorithmen entwickelt und implementiert, die stabil und frei von numerischer Diffusion sind. Um das Auftreten von Interpolationsfehlern zu vermeiden, wird ein integriertes GRW-Lösungsverfahren entwickelt, das Geschwindigkeiten und Konzentrationen auf dem selben regulären Gitter berechnet. Wir nutzen grobkörnige (engl. Coarse grained) (CG) Mittelwerte in Raum und Zeit über die Trajektorien der berechneten Partikel, die die Konzentrationen der reaktiven chemischen Spezies in den GRWSimulationen beschreiben. Diese werden genutzt, um eine kontinuierliche Beschreibung der Transportprozesse zu erhalten. Nachdem die Mittelungsprozedur die Variation der simulierten Konzentrationen reduziert, genügt eine relativ kleine Anzahl von Monte Carlo - Simulationen, um die statistischen Kennzahlen zu gewinnen, und gleichzeitig der Auswirkung der Raum-Zeit-Skalen der hydrologischen Beobachtungen Rechnung zu tragen. Des weiteren können lokale Bilanzgleichungen für die CG Raum-Zeit-Mittel genutzt werden, um die hochskalierten Diffusionskoeffizienten und Reaktionsterme zu berechnen.
Agriculture is the major contributor of nitrogen to ecosystems, both by organic and inorganic fertilizers. Percolation of nitrate to groundwater and further transport to surface waters is assumed to be one of the major pathways in the fate of this nitrogen. The quantification of groundwater and associated nitrate flux to streams is still challenging. In particular because we lack understanding of the spatial distribution and temporal variability of groundwater and associated NO3- fluxes. In this preliminary study we will focus on the identification and quantification of groundwater and associated nitrate fluxes by combining high resolution distributed fiber-optic temperature sensing (DTS) with in situ UV photometry (ProPS). DTS is a new technique that is capable to measure temperature over distances of km with a spatial resolution of ca1 m and an accuracy of 0.01 K. It has been applied successfully to identify and quantify sources of groundwater discharge to streams. ProPS is a submersible UV process photometer, which uses high precision spectral analyses to provide single substance concentrations, in our case NO3-, at minute intervals and a detection limit of less than 0.05 mg l-1 (ca.0.01 mg NO3--Nl-1). We will conduct field experiments using artificial point sources of lateral inflow to test DTS and ProPS based quantification approaches and estimate their uncertainty. The selected study area is the Schwingbach catchment in Hessen, Germany, which has a good monitoring infrastructure. Preliminary research on hydrological fluxes and field observations indicate that the catchment favors the intended study.
Messungen der Verhältnisse stabiler Isotope in flüchtigen organischen Verbindungen (VOC) in der Atmosphäre liefern wichtige Informationen über die Quellen, die photochemische Geschichte, die Aufenthaltszeiten und die Bilanzen dieser Verbindungen. Bisherige Studien haben sich ausschließlich mit den Verhältnissen stabiler Kohlenstoffisotope in diesen Verbindungen beschäftigt. Die Untersuchung der Isotopenverhältnisse anderer Elemente kann dazu beitragen, atmosphärische Prozesse noch besser zu verstehen und zu quantifizieren. Am vielversprechendsten sind dabei die Verhältnisse der stabilen Wasserstoffisotope, weil auf Grund des im Vergleich zu Kohlenstoff höheren Masseverhältnisses deutlich ausgeprägter Isotopeneffekte zu erwarten sind. Wir beabsichtigen, die Verhältnisse stabiler Wasserstoff-Isotope in atmosphärischen VOC mit einem Gaschromatograph-Pyrolyse-Isotopenverhältnis-Massenspektrometer (GC-P-IRMS) zu messen. Dazu haben wir eine Methode entwickelt, die auf einer Modifikation der bisherigen Messungen stabiler Kohlenstoff-Isotope in atmosphärischen VOC beruht. Um die für diese Messungen notwendigen Nachweisgrenzen und Reproduzierbarkeiten zu gewährleisten, ist die Anreicherung der VOC aus einer großen Probenmenge (je nach Konzentration der VOC bis zu 200 L Luft) notwendig. Dazu wurde das vorhandene Probenaufbereitungssystem modifiziert. Die Methode ist inzwischen gut charakterisiert. Wir konnten zeigen, dass die Nachweisgrenzen ausreichen, um die in der Atmosphäre erwarteten Änderungen der Isotopenverhältnisse durch chemische und physikalische Prozesse nachweisen zu können. Erste Messungen von VOC aus der Umgebungsluft ergaben vielversprechende Ergebnisse. Es ist geplant, basierend auf den bisherigen Erfahrungen das Anreicherungssystem umzubauen, um eine bessere Reduzierung von Wasser und Kohlendioxid aus der Luftprobe zu erreichen sowie durch die Wahl neuer Adsorbentien die Anreicherung zu optimieren und das Spektrum der messbaren VOC zu erweitern. Parallel dazu werden fehlende kinetische Isotopeneffekte gemessen sowie Quellstudien durchgeführt. Anschließend sollen in einer einjährigen Studie Tages- und Jahresgänge ausgewählter VOC untersucht werden. Parallel dazu sollen bestehende Interpretationsmethoden und Anwendungsmöglichkeiten weiterentwickelt werden. Die vorgeschlagene Methode ist ein empfindliches Werkzeug, um die Quellen von VOC zu identifizieren, photochemische Prozesse sowie den Einfluss von Chemie und Transport auf ihre Verteilung zu untersuchen und ihre Aufenthaltszeiten in der Atmosphäre zu bestimmen. Unseres Wissens gibt es bisher keine Messungen der Verhältnisse stabiler Wasserstoff-Isotope in VOC in der Umgebungsluft. Diese Messungen werden weitere Bausteine zum Verständnis chemischer und physikalischer Prozesse in der Atmosphäre liefern.
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.
Die Sea-Surface Microlayer (SML) als dünne Grenzschicht trennt Hydrosphäre und Atmosphäre. Häufig sind die Konzentrationen bestimmter Verbindungen in der SML höher, entweder durch physikalische Konzentration aus dem darunter liegenden Wasser, durch Produktion in der SML oder durch atmosphärische Ablagerungen. Ein bekannter Aspekt ist die durchweg höhere Konzentration von chromophoren gelösten organischen Stoffen (CDOM) in der SML im Vergleich zum darunter liegenden Wasser. Kürzlich haben wir gezeigt, dass die inhärenten optischen Eigenschaften (IOP) â€Ì d.h. die Lichtstreu- und Absorptionseigenschaften von Wasser und seinen Bestandteilen â€Ì der SML genutzt werden können Komponenten in der SML zu charakterisieren und nützliche Informationen für den Strahlungstransfer und für Fernerkundungsstudien zu liefern. Darüber hinaus war unsere frühere Forschung zu optischen Eigenschaften in der SML unsere Motivation hier vorzuschlagen, IOPs und apparente optischen Eigenschaften (AOPs) â€Ì abgeleitet aus spektralradiometrischen Messungen des Lichtfeldes â€Ì sowie die Fluoreszenz zur Charakterisierung von organischen Stoffen (OM) und deren Transformation für die Echtzeitbewertung der SML als biologischen und chemischen Lebensraum zu nutzen. Hiermit können wir in außergewöhnlicher Weise die Kurzzeitdynamik relevanter biologischer und chemischer Treiber in der SML untersuchen.
In subsoils, organic matter (SOM) concentrations and microbial densities are much lower than in topsoils and most likely highly heterogeneously distributed. We therefore hypothesize, that the spatial separation between consumers (microorganisms) and their substrates (SOM) is an important limiting factor for carbon turnover in subsoils. Further, we expect microbial activity to occur mainly in few hot spots, such as the rhizosphere or flow paths where fresh substrate inputs are rapidly mineralized. In a first step, the spatial distribution of enzyme and microbial activities in top- and subsoils will be determined in order to identify hot spots and relate this to apparent 14C age, SOM composition, microbial community composition and soil properties, as determined by the other projects within the research unit. In a further step it will be determined, if microbial activity and SOM turnover is limited by substrate availability in spatially distinct soil microsites. By relating this data to root distribution and preferential flow paths we will contribute to the understanding of stabilizing and destabilizing processes of subsoil organic matter. As it is unclear, at which spatial scale these differentiating processes are effective, the analysis of spatial variability will cover the dm to the mm scale. As spatial segregation between consumers and substrates will depend on the pore and aggregate architecture of the soil, the role of the physical integrity of these structures on SOM turnover will also be investigated in laboratory experiments.
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.
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