Es wird vermutet, dass Zirruswolken in hohen geographischen Breiten (arktische Zirren), einen positiven „Cloud Radiative Effect“ (CRE) haben und somit zum Phänomen der "Arctic Amplification" beitragen. Das Vorzeichen und die Stärke des CRE arktischer Zirren hängt von deren mikrophysikalischen Eigenschaften, d.h. der Eispartikelkonzentration, dem effektiven Eispartikelradius und dem Eiswassergehalt (IWC), ab. Diese Parameter werden hauptsächlich durch den Eisbildungsprozess (heterogen vs. homogen) und durch den Bildungspfad (in-situ vs. flüssiger Ursprung) bestimmt. Dies impliziert insbesondere für Zirren flüssigen Ursprungs die Beteiligung von eisnukleierenden Partikeln (INP), was deren Häufigkeit, Eigenschaften und Quellen zu Schlüsselfaktoren für die Bildung, die mikrophysikalischen und Strahlungseigenschaften von Zirren in hoher Breiten macht. Informationen über INP in hohen geographischen Breiten im Allgemeinen und in größeren Höhen im Besonderen, extrem rar. Im Rahmen der HALO-Mission CIRRUS-HL wollen wir daher das Wissen hinsichtlich arktischer INP über a) die Charakterisierung von Eispartikel- (IPR) und Wolkentröpfchenresiduen (CPR, Summe aus IPR und Tröpfchenresiduen) in arktischen Zirren und Mischphasenwolken, und b) die vertikal aufgelöste Messung (Mischphase bis Zirrusniveau) von Hochtemperatur INP (> -30°C) außerhalb von Wolken, erweitern. Für die geplanten Untersuchungen werden der HALO-CVI („Counterflow Virtual Impactor“) und der Aerosolpartikelfiltersammler HERA verwendet werden. Hinter dem HALO-CVI werden Instrumente zur physikalischen (Anzahl der Konzentrationen, Partikelgrößenverteilung, BC-Konzentration) und chemischen (Einzelpartikelzusammensetzung, MPI-C) Charakterisierung der IPR und CPR betrieben. Die von HERA gesammelten Filterproben werden im Anschuss an die Kampagne in den TROPOS-Laboratorien hinsichtlich der physikalischen INP-Eigenschaften (Anzahlkonzentrationen und Gefrierspektren) sowie der chemischen Zusammensetzung der Aerosolpartikel analysiert.Bei In-Wolken-Messungen werden der HALO-CVI und HERA kombiniert werden. So können die INP, innerhalb der gesammelten IPR (Zirren) und Wolkentropfenresiduen (CPR, in Mischphasenwolken) identifiziert, quantifiziert und charakterisiert werden. Diese INP könnten potenzielle Vorläufer von Zirrus mit flüssigem Ursprung in hohen Breiten sein.In Verbindung mit den Ergebnissen der im Rahmen von CIRRUS-HL durchgeführten in-situ Messungen wolkenmikrophysikalischer Eigenschaften, sowie der Analyse von Rückwärtstrajektorien der untersuchten Luftmassen werden wir a) bzgl. der Häufigkeit und der Eigenschaften von INP ein bisher einmaliges Schließungsexperiment (innerhalb und außerhalb der Wolke) durchführen, b) das Wissen über die raumzeitliche Verteilung, die Eigenschaften und die Quellen von INP signifikant erweitern und c) tiefe Einblicke in INP-Effekte auf die Bildung und die mikrophysikalischen Eigenschaften von Zirruswolken in hohen geographischen Breiten erhalten.
Viele Pflanzenschutzmittel bilden nicht extrahierbare Rueckstaende im Boden, die konventionellen analytischen Methoden nicht zugaenglich sind. Untersuchungen dieser Pestizidfraktion deuten darauf hin, dass die Belastung des Bodens mit Pflanzenschutzmitteln bisher moeglicherweise unterschaetzt wurde. Das Herbizid Bentazon wird im Boden ueberwiegend in Huminstoffe eingebaut. Da Regenwuermer grosse Bedeutung fuer die Umsetzung organischer Materialien, insbesondere Huminstoffen, haben, wird in Laborexperimenten der Einfluss dieser Tiergruppe auf die Bindung von radioaktiv markierten Bentazonrueckstaenden untersucht. Ferner werden Veraenderungen des Metabolitspektrums im Boden und die Verteilung von Bentazon in Regenwuermern analytisch und autoradiographisch erfasst.
The site of the heating power station and former gasworks in Plauen is contaminated over a wide area with pollutants specific to gasworks - above all BTX aromatics, PAH (polycyclic aromatic hydrocarbons), tar oils, phenols and ammonium - down to a depth of six metres. According to expert opinion, a soil volume of some 20000 m3 must urgently be cleaned up. A remediation concept has been prepared at the request of the municipality of Plauen, based on the use-related potential assessment for the site. The assessment concludes that there is an acute environmental hazard for the directly adjoining river 'Weisse Elster'. The approach pursued in this project represents a new solution to the problem of contaminated sites. Instead of using ex-situ methods for carrying out a complete cleanup of the contaminated site, as practised so far, in-situ methods are used. In this way, the acute hazard potential is eliminated, leaving only a tolerable amount of residual pollution. This objective will be achieved through a combination of pneumatic, hydraulic and microbiological in-situ measures. The efficiency will be further increased by specific pollutant mobilization. The technical feasibility has been confirmed by soil air suction tests and pumping tests on sites as well as microbiological laboratory analyses. The in-situ decontamination is superior to the traditional ex-situ methods in terms of economic efficiency, waste prevention and reducing traffic movements. The innovative methods proposed here involve, in particular, hot-steam injections and controlled oxyhydrogen gas explosions that will increase the availability of immobile pollutants attached to the soil grain.
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.
The interest in the reuse of water treatment residuals (WTR) as a low-cost alternative to commercial adsorbents for metal removal from aqueous solutions has been growing in recent years. In this study, Fe-WTR and Mn-WTR from a pilot-scale groundwater treatment plant were investigated for their potential to remove As(III), Cd(II), Cu(II), Ni(II) and Pb(II) from different water matrices and at different pH values in batch tests. WTR compositions were compared with chemical and microscopic analyses, revealing that Mn-WTR had a higher Mn content and a slightly higher pHPZC than Fe-WTR. In kinetic experiments at pH 7.0, metal adsorption onto Fe-WTR was faster than adsorption onto Mn-WTR, while final loadings were higher on Mn-WTR. Ni(II) and Cd(II) showed higher affinities for Mn-WTR, while the adsorption capacity of Fe-WTR was exhausted after short contact times. The Elovich model was best suited to describe experimental data, indicating chemisorption as the dominant adsorption mechanism. Isotherm experiments in multi-solute solutions showed that As(III) and Pb(II) removals increased with decreasing pH, while Cd(II) and Ni(II) removals increased with increasing pH. Except for Pb(II), adsorption could be explained with electrostatic interactions between adsorbate and adsorbent, and precipitation likely played a role in metal removal. The Langmuir model described the data better than the Freundlich model in most cases. However, models were unable to represent competition that clearly occurred at higher initial concentrations. Fe-WTR was better suited for metal adsorption in most cases; yet Mn-WTR was more effective for the adsorption of Cd(II) and Ni(II). © 2026 The Authors
Excess dissolved carbon dioxide (CO2) is frequently encountered in natural groundwaters, originating from both geochemical and biological processes. In the investigated case, contamination of groundwater with toxic hexavalent chromium (Cr(VI)) occurred due to anthropogenic activities. The co-occurrence of CO2 and Cr(VI) posed a distinct challenge for water treatment, as multiple process steps need to be tailored to remove both substances at the same time. This study investigates an integrated treatment approach specifically developed for groundwater containing elevated levels of both Cr(VI) and CO2. The process combines reduction coagulation filtration (RCF) with ferrous iron (Fe(II)) dosage with limestone filtration for concurrent Cr(VI) removal and water deacidification. A pilot plant with two parallel filters—one filled with dense limestone and the other with porous limestone—was operated under varying Fe(II) dosages (Fe(II), 0.3–1.0 mg/L) and filtration velocities (4.4–15.5 m/h). Results demonstrate that the RCF process achieved efficient Cr(VI) removal at moderate Fe(II) concentrations (<1.0 mg/L), with no breakthrough or reoxidation observed. Limestone filtration efficiently increased pH, calcium concentration, and buffer capacity, thereby decarbonating the water. Porous limestone showed higher reactivity than the dense limestone commonly used. Analysis of backwash sludge confirmed stable chromium retention and low residual metal concentrations in the supernatant. These findings confirm that the integrated RCF–limestone process provides an effective and cost-efficient solution for treating groundwater impacted by anthropogenic Cr(VI) and naturally elevated CO2 concentration. © 2026 The Authors.
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.
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 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.
Ecosystem models often use wet weights to parameterise biota disregarding their water content. This may be especially erroneous for gelatinous plankton, such as salps and pyrosomes, with high, compared to crustaceans, water content. Poorly quantified residual water should also be corrected when using dry weights for parameterisation. We estimated the residual water content (as well as elemental and organic contents) for seven tunicate species, one pyrosome and six salps (N = 107). Specimens were collected during several research expeditions in the Southern Ocean, the Northeast Pacific, east of New Zealand, and around Hawaii between 2004 and 2021. The residual water content of tunicates was analyzed for inter- and intraspecific variability. The H-surplus method (Madin et al. 1981) was applied for the residual water content calculation. The dataset contains information about the life cycle stage (blastozooid versus oozooid), tissue type (tunic versus whole organism), drying method (oven versus freeze-drying), size, and the elemental and organic contents of the samples. The methods and results of the study are described in detail in Lüskow et al. (submitted).
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