Steroid hormones are essential in orchestrating oocyte maturation, i.e. estrogens of follicular origin support the development of the female gamete and fertilization. In this project the concentration of free and conjugated estrogens during follicular development will be analysed and compared to local concentrations in the developing follicle. Cattle are suitable animal models because of the accessibility and suitability for frequent examination and sampling. Furthermore, it has been useful for understanding several features of human reproduction including follicular dynamics, the fate of the emerging follicles is orchestrated mainly by gonadotropins and steroid hormones in a similar manner. Ovarian SULT1E1 participates locally in the regulation of follicular estrogen activity. The ESTcatalysed down-regulation of estrogen activity enables normal ovulation. Conversely, sulfoconjugated estrogens may also be precursors of the production of free estrogens depending on estrogen sulfatase (StS) acitivity. In mammals, follicular luteinisation/ovulation is triggered by a surge in LH and is characterised by numerous physical and biochemical changes, including the decreased production of estradiol (E2). This loss in E2 biosynthetic capacity has been explained by a marked decrease in the expression of key steroidogenic enzymes involved in the follicular production of active estrogens. However, little is known about the regulation of enzymes/proteins responsible for the inactivation and elimination of estrogens, as mediated for example by EST during this period.
The goal of this project is to capture and analyse fluctuations of the fresh water in the western Nordic Seas and to understand the related processes. The East Greenland Current in the Nordic Seas constitutes an important conduit for fresh water exiting the Arctic Ocean towards the North Atlantic. The Arctic Ocean receives huge amounts of fresh water by continental runoff and by import from the Pacific Ocean. Within the Arctic Ocean fresh water is concentrated at the surface through sea ice formation. The East Greenland Current carries this fresh water in variable fractions as sea ice and in liquid form; part of it enters the central Nordic Seas, via branching of the current and through eddies. It controls the intensity of deep water formation and dilutes the water masses which result from convection. The last decades showed significant changes of the fresh water yield and distribution in the Nordic Seas and such anomalies were found to circulate through the North Atlantic. In this project the fresh water inventory, its spatial distribution and its pathways between the East Greenland Current and the interior Greenland and Icelandic seas shall be captured by autonomous glider missions. The new measurements and existing data will, in combination with the modeling work of the research group, serve as basis for understanding the causes of the fresh water variability and their consequences for the North Atlantic circulation and deep water formation.
Labor- und Feldstudien zeigen, dass die Oberflächengrenzschicht des Ozeans (â€Ìsurface microlayerâ€Ì, kurz SML) die biogeochemischen Kreisläufe von klimaaktiven und atmosphärisch wichtigen Spurengasen wie Kohlenstoffdioxid (CO2), Kohlenstoffmonoxid (CO), Methan (CH4), Lachgas (N2O) und Dimethylsulfid (DMS) stark beeinflusst: (i) Jüngste Studien aus den PASSME- und SOPRAN-Projekten haben hervorgehoben, dass Anreicherungen von oberflächenaktiven Substanzen (d.h. Tensiden) einen starken (dämpfenden) Effekt sowohl auf die CO2- als auch auf die N2O-Flüsse über die SML/Atmosphären-Grenzfläche hinweg haben und (ii) Spurengase können durch (mikro)biologische oder (photo)chemische Prozesse in der SML produziert und verbraucht werden. Daher kann der oberste Teil des Ozeans, einschließlich der SML, verglichen mit dem Wasser, das in der Mischungsschicht unterhalb der SML zu finden ist, eine bedeutende Quelle oder Senke für diese Gase sein, was von sehr großer Relevanz für die Forschungseinheit BASS ist. Die Konzentrationen von CO2, N2O und anderen gelösten Gasen in der SML (oder den oberen Zentimetern des Ozeans) unterscheiden sich nachweislich von ihren Konzentrationen unterhalb der SML. Typischerweise werden die Nettoquellen und -senken wichtiger atmosphärischer Spurengase mit Konzentrationen berechnet, die in der Mischungsschicht gemessen wurden und mit Gasaustauschgeschwindigkeiten, die die SML nicht berücksichtigen. Diese Diskrepanzen führen zu falsch berechneten Austauschflüssen, die in der Folge zu großen Unsicherheiten in den Berechnungen der Klima-Antrieben und der Luftqualität in Erdsystemmodellen führen können. Durch die Verknüpfung unserer Spurengasmessungen mit Messungen von (i) der Dynamik und den molekularen Eigenschaften der organischen Materie und speziell des organischen Kohlenstoffs (SP1.1; SP1.5), (ii) der biologischen Diversität und der Stoffwechselaktivität (SP1.2), (iii) den optischen Eigenschaften der organischen Materie (SP1.3), (iv) der photochemischen Umwandlung der organischen Materie (SP1.4) und (v) den physikalischen Transportprozessen (SP2.3) werden wir ein umfassendes Verständnis darüber erlangen, wie die SML die Variabilität der Spurengasflüsse beeinflusst.
Gasaustausch findet in der Atmosphäre primär durch turbulenten und laminaren Fluss statt. Im Boden dagegen spielt advektiver Gastransport eine untergeordnete Rolle, stattdessen dominiert Diffusion die Transportprozesse. Trotz der Unterschiedlichkeit und scheinbaren Unabhängigkeit dieser Prozesse wurde während Freilanduntersuchungen ein Anstieg von Gastransportraten im Boden um mehrere 10 % während Phasen starken Windes beobachtet. Dieser Anstieg ist auf wind-induzierte Druckfluktuationen zurückzuführen, die sich in das luftgefüllte Porensystem des Bodens fortpflanzen und zu einem minimal oszillierenden Luftmassenfluss führen (Pressure-pumping Effekt). Durch den oszillierenden Charakter des Luftmassenflusses ist der direkte Beitrag zum Gastransport sehr gering. Die damit einhergehende Dispersion führt jedoch zu einem Anstieg der effektiven Gastransportrate entgegen des Konzentrationsgradienten. Wird der Pressure-pumping (PP) Effekt bei der Bestimmung von Gasflüssen mit der Gradienten- und Kammermethode nicht berücksichtigt, kann dies zu großen Unsicherheiten in der Bestimmung von Bodengasflüssen führen. Insbesondere für das langfristige Monitoring von treibhausrelevanten Gasflüssen stellen diese Unsicherheiten ein zentrales Problem dar. Wir stellen vier Hypothesen auf:(H1) Der PP-Effekt ist abhängig von Bodeneigenschaften.(H2) Die Ausprägung von Luftdruckfluktuationen ist abhängig von der Rauigkeit verschiedener Landnutzungen (Wald, Grasland, landwirtschaftliche Kulturen, Stadt)(H3) Kammermessungen werden durch Luftdruckfluktuationen beeinflusst.(H4) Der Austausch und Umsatz von Methan in Böden von Mittelgebirgswäldern wird durch den PP-Effekt verstärkt. Die Hypothesen 1, 3 und 4 werden mittels Laboruntersuchungen von Proben verschiedener Böden und Bodenfeuchtebedingungen überprüft. Die Hypothese 2 wird durch Freilandmessungen an verschiedenen Standorten überprüft. Ziele des Vorhabens sind: (Z1) Modelle zu entwickeln, die die Quantifizierung des Einflusses der Bodenstruktur auf den PP-Effekt ermöglichen, (Z2) den Effekt der Oberflächenrauigkeit auf Luftdruckschwankungen zu quantifizieren, (Z3) Schwellenwerte zu definieren, die die Bestimmung von Standorten mit ausgeprägtem PP-Effekt ermöglichen, (Z4) Faktoren für die Berücksichtigung des PP-Effekts für Kammermessungen zu entwickeln, (Z5) Faktoren für die Berücksichtigung des PP-Effekts für die Gradienten Methode zu entwickeln, (Z6) den Einfluss des PP-Effekts auf die Methanaufnahme von Böden in Mittelgebirgswäldern zu bestimmen. Ein besseres Verständnis des bisher nur unzureichend untersuchten PP-Effekts wird wesentlich dazu beitragen, die Verlässlichkeit und Präzision von Messungen von Bodengasflüssen zu steigern, die die Grundlage für weitergehende Forschung darstellen.
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.
We propose to use positron emission tomography (PET) for imaging of tracer migration in a soil horizon, to be coupled with image simulation using the lattice Boltzmann equation (LBE) modeling approach. PET enables direct visualization of inert KF or KBr solute migration at the soil horizon scale, but also reactive halogenated organic target (2,4-D and MCPA) compound migration down to nM concentrations once radiolabelling with 18F or 76Br marker is achieved. Retardation at biogeochemical interfaces with different sorption properties will thus be imaged in-situ. Theoretical image simulation for process verification will be enabled by introducing a multi-grid approach and additional kinetic boundary conditions in the parallelized LBE solver. As a boundary condition for the latter, the real pore scale and distribution of biogeochemical interfaces will be derived by X-ray computer-tomography (XCT) down to 300 nm spatial voxel resolution. The aim is to produce by both approaches velocity field movies due to heterogeneous biogeochemical retardation of the target compounds with high resolution in both the spatial and temporal scale (4D).
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.
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.
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.
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.
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