This dataset contains calculated carbonate chemistry parameters, including the concentrations of dissolved CO2, HCO3-, CO32- and dissolved inorganic carbon, the fugacity and partial pressure of CO2 and the saturation states of aragonite (Ωarag) and calcite (Ωcalc), for the alkalization mesocosms. Values were calculated from pH, total alkalinity, salinity and temperature measured between 17 April and 19 June 2024, using the seacarb package (Orr et al., 2018) in R (V. 4.3.2). Measured pH values, which refer to the NBS scale, were first converted to the total scale using the total proton activity coefficient fH of Takahashi et al. (1982), lowering pH by 0.12 to 0.13 units across the measured salinity and temperature range. Calculations used the carbonic acid dissociation constants of Lueker et al. (2000), the bisulfate dissociation constant of Dickson (1990), the hydrogen fluoride constant of Perez & Fraga (1987), total boron after Uppström (1974) and the aragonite and calcite solubility products of Mucci (1983), all evaluated at in situ temperature and salinity. The conversion from the NBS to the total scale carries a residual uncertainty of about 0.01 to 0.02 pH units, because the liquid junction potential between the dilute calibration buffers and seawater is not fully captured by fH. This propagates to an uncertainty of roughly 5 to 15 % in calculated pCO2 and a correspondingly smaller uncertainty in the saturation states.
This dataset contains calculated carbonate chemistry parameters, including the concentrations of dissolved CO2, HCO3-, CO32- and dissolved inorganic carbon, the fugacity and partial pressure of CO2 and the saturation states of aragonite (Ωarag) and calcite (Ωcalc), for the exposure mesocosms. Values were calculated from pH, total alkalinity, salinity and temperature measured between 8 May and 10 July 2024, using the seacarb package (Orr et al., 2018) in R (V. 4.3.2). Measured pH values, which refer to the NBS scale, were first converted to the total scale using the total proton activity coefficient fH of Takahashi et al. (1982), lowering pH by 0.12 to 0.13 units across the measured salinity and temperature range. Calculations used the carbonic acid dissociation constants of Lueker et al. (2000), the bisulfate dissociation constant of Dickson (1990), the hydrogen fluoride constant of Perez & Fraga (1987), total boron after Uppström (1974) and the aragonite and calcite solubility products of Mucci (1983), all evaluated at in situ temperature and salinity. The conversion from the NBS to the total scale carries a residual uncertainty of about 0.01 to 0.02 pH units, because the liquid junction potential between the dilute calibration buffers and seawater is not fully captured by fH. This propagates to an uncertainty of roughly 5 to 15 % in calculated pCO2 and a correspondingly smaller uncertainty in the saturation states.
This dataset is supplemental to the paper Wiesman et al. (submitted) and contains data on the density of dislocations and their stress fields in olivine rocks deformed via laboratory experiments. The data were used to investigate how the quality of diffraction patterns obtained via electron backscatter diffraction (EBSD) affect the stress maps and geometrically necessary dislocation (GND) maps obtained via analysis with high-angular resolution electron backscatter diffraction (HR-EBSD). These results can be used to optimize the patterns collected during EBSD to reduce noise in the HR-EBSD analysis. Data are provided in a zip folder and include: • Measurements of lattice orientation via EBSD: six raw .ctf files and six processed .ctf files of regions mapped with HR-EBSD • Examples of electron backscatter diffraction patterns used to calculate radial power spectra: 12 .tiff files of diffraction patterns • Densities of geometrically necessary dislocations from the HR-EBSD analysis: six .txt files of processed data • Residual stress heterogeneity also determined from HR-EBSD analysis: six .txt files of processed data Data types and the number of frames averaged are also indicated in the file names. Files are organized into folders by the number of frames averaged. A full description is available in the data description file.
Das Auslaugverfahren nach DEV S4 soll durch ein Schnellauslaugverfahren ergänzt werden, mit dem industrielle Nebenprodukte und RC-Baustoffe in ca. 30 Minuten in vergleichbarer Weise eluiert werden können wie nach dem Normverfahren. Das Verfahren soll so weit optimiert werden, dass es zur Eingangskontrolle bei der Anlieferung von Baustoffen zugelassen werden kann. Es sollen verschiedene Ultraschallsysteme erprobt und die Randbedingungen des Verfahrens so variiert werden, dass die Ergebnisse weitgehend denen aus dem modifizierten S4-Verfahren gleichen. Das Verfahren wird an auseinandergesiebten und nach vorgegebener Sieblinie zusammengesetzten Rückstellproben sowie an weiteren praxisrelevanten Baustoffen erprobt. Durch Vergleich mit laufenden praxisgerechten Feldversuchen an RC-Baustoffen können die für Routineanalysen wichtigen Parameter ermittelt werden. Eine Schnelluntersuchung einschließlich der Analyseverfahren soll modellhaft vorgeschlagen werden.
Erstellung zuverlaessiger Schnelltests zur Erfassung gebundener Rueckstaende in Nahrungsmittel (pflanzliche Erzeugung).
Feedlots sind v.a. in Nordamerika verbreitete Tierproduktionsbetriebe mit intensivster Freilandhaltung. Es wird vermutet, dass Feedlots Brennpunkte einer Umweltbelastung mit pharmazeutischen Antibiotika sind, da große Tierbestände gehalten werden, die regelmäßig Antibiotika erhalten. Es wurden Bodenproben von einer Grasland-Kontrolle sowie Boden- und Tierdung-Proben von Bodenprofilen eines gewerblichen und eines experimentellen Feedlots entnommen und analysiert. Rückstände der üblicherweise verwendeten Antibiotika Sulfamethazin, Chlortetracyclin und Tylosin wurden mit unterschiedlichen Konzentrationen in Dung, Boden und Wasser gefunden. Die Ergebnisse weisen auf eine nicht unerhebliche Persistenz, Tiefenverlagerung und insbesondere Oberflächenabfluss der Antibiotika Sulfamethazin und Chlortetracyclin hin.
In structured soils, the interaction of percolating water and reactive solutes with the soil matrix is mostly restricted to the surfaces of preferential flow paths. Flow paths, i.e., macropores, are formed by worm burrows, decayed root channels, cracks, and inter-aggregate spaces. While biopores are covered by earthworm casts and mucilage or by root residues, aggregates and cracks are often coated by soil organic matter (SOM), oxides, and clay minerals especially in the clay illuviation horizons of Luvisols. The SOM as well as the clay mineral composition and concentration strongly determine the wettability and sorption capacity of the coatings and thus control water and solute movement as well as the mass exchange between the preferential flow paths and the soil matrix. The objective of this proposal is the quantitative description of the small-scale distribution of physicochemical properties of intact structural surfaces and flow path surfaces and of their distribution in the soil volume. Samples of Bt horizons of Luvisols from Loess will be compared with those from glacial till. At intact structural surfaces prepared from soil clods, the spatial distribution (mm-scale) of SOM and clay mineral composition will be characterized with DRIFT (Diffuse reflectance infrared Fourier transform) spectroscopy using a self-developed mapping technique. For samples manually separated from coated surfaces and biopore walls, the contents of organic carbon (Corg) and the cation exchange capacity (CEC) will be analyzed and related to the intensities of specific signals in DRIFT spectra using Partial Least Square Regression (PLSR) analysis. The signal intensities of the DRIFT mapping spectra will be used to quantify the spatial distribution of Corg and CEC at these structural surfaces. The DRIFT mapping data will also be used for qualitatively characterizing the small scale distribution of the recalcitrance, humification, and microbial activity of the SOM from structural surfaces. The clay mineral composition of defined surface regions will be characterized by combining DRIFT spectroscopic with X-ray diffractometric analysis of manually separated samples. Subsequently, the spatial distribution of the clay mineral composition at structural surfaces will be determined from the intensities of clay mineral-specific signals in the DRIFT mapping spectra and exemplarily compared to scanning electron microscopic and infrared microscopic analysis of thin sections and thin polished micro-sections. The three-dimensional spatial distribution of the total structural surfaces in the volume of the Bt horizons will be quantified using X-ray computed tomography (CT) analysis of soil cores. The active preferential flow paths will be visualized and quantified by field tracer experiments. These CT and tracer data will be used to transfer the properties of the structural surfaces characterized by DRIFT mapping onto the active preferential flow paths in the Bt horizons.
This data set was recorded by permanently installed above-water radiometry onboard RV HEINCKE. Five TriOS instruments are installed at the top of the foremast: one irradiance sensor (ACC) to measure the incoming solar irradiance as a reference, 2 radiometers (ARC) to measure the incoming sky radiance, 2 radiometers (ARC) to measure the sea-surface leaving radiance. One set of radiometers is pointed to 45° starboard and the other to 45° port. The data were recorded with the MSDA-XE software in 15s interval and transferred via cloud. The data were then reformatted and processed with the community processor HyperCP. Ancillary data was taken from the mastertrack and Insightics DSHIP extraction. Data were processed for coastal conditions using sky/sunglint correction by Zhang et al. (2017), NIR residual correction using Ruddick et al. 2006, and BRDF correction based on IOP-based approach by Lee.
Feststellung messbarer Rueckstaende im Wildtier bei gleichzeitiger Aufnahme von Wirkstoff-Kombinationen aus der Nahrung und ihr Einfluss auf die Verteilung und Rueckstandsbildung im Tierkoerper. Die Umweltchemikalien werden allein und in Kombination im Koernerfutter verabreicht. In regelmaessigen Abstaenden werden Organ- und Depotfett- und Muskelproben entnommen. Die Rueckstaende werden gaschromatisch bestimmt. Ueber den gesamten Zeitraum wird mit geeigneten Parametern die biologische Leistungsfaehigkeit ermittelt. Feststellung moeglicher gegenseitiger Beeinflussung im Sinne von Synergismus oder Antagonismus.
a) Feststellung des Gehalts an Pflanzenschutzrueckstaenden in verschiedenen Getreidearten. Untersuchung des Abbaus bzw. des Metabolismus waehrend der Lagerung und waehrend der Verarbeitung. b) Analytische Bestimmung der Pestizide in Getreide und in Mahlprodukten in Abhaengigkeit von Lagerung und Verarbeitung einschliesslich Backprozess. Feststellung von Stoffwechselprodukten. c) Mehrjaehrige, laufende Untersuchungen in Anpassung an neue Pflanzenschutzmittel und neue analytische Verfahren.
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