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Site information for porewater chemistry survey of European peatlands

The study investigates the chemical and physical characteristics of porewater and soil samples from peatlands across 64 sites in Germany, Poland, Estonia, Scotland, Sweden, and Georgia sampled between 1997 and 2017. The sites covers oceanic (Cfb, Cfc) and continental (Dfb, Dfc) climate zones and include both minerotrophic fens and ombrotrophic bogs. Fens were further classified into poor and rich types based on acidity and floristic composition, with rich fens characterized by higher pH and calcium concentrations due to mineral-rich groundwater inputs. The study also distinguishes between natural sites with stable near-surface water tables and rewetted sites previously subjected to drainage and agricultural use.

Geochemical parameters in peat depth profiles from ombrotrophic bogs in North and Central Europe. Fochteloër Veen, the Netherlands

This dataset contains geochemical variables measured in six depth profiles from ombrotrophic peatlands in North and Central Europe. Peat cores were taken during the spring and summer of 2022 from Amtsvenn (AV1), Germany; Drebbersches Moor (DM1), Germany; Fochteloër Veen (FV1), the Netherlands; Bagno Kusowo (KR1), Poland; Pichlmaier Moor (PI1), Austria and Pürgschachen Moor (PM1), Austria. The cores AV1, DM1 and KR1 were taken using a Wardenaar sampler (Royal Eijkelkamp, Giesbeek, the Netherlands) and had diameter of 10 cm. The cores FV1, PM1 and PI1 had an 8 cm diameter and were obtained using an Instorf sampler (Royal Eijkelkamp, Giesbeek, the Netherlands). The cores FV1, DM1 and KR1 were 100 cm, core AV1 was 95 cm, core PI1 was 85 cm and core PM1 was 200 cm. The cores were subsampeled in 1 cm (AV1, DM1, KR1, FV1) and 2 cm (PI1, PM1) sections. The subsamples were milled after freeze drying in a ballmill using tungen carbide accesoires. X-Ray Fluorescence (WD-XRF; ZSX Primus II, Rigaku, Tokyo, Japan) was used to determine Al (μg g-1), As (μg g-1), Ba (μg g-1), Br (μg g-1), Ca (g g-1), Cl (μg g-1), Cr (μg g-1), Cu (μg g-1), Fe (g g-1), K (g g-1), Mg (μg g-1), Mn (μg g-1), Na (μg g-1), P (μg g-1), Pb (μg g-1), Rb (μg g-1), S (μg g-1), Si (μg g-1), Sr (μg g-1), Ti (μg g-1) and Zn (μg g-1). These data were processed and calibrated using the iloekxrf package (Teickner & Knorr, 2024) in R. C, N and their stable isotopes were determined using an elemental analyser linked to an isotope ratio mass spectrometer (EA-3000, Eurovector, Pavia, Italy & Nu Horizon, Nu Instruments, Wrexham, UK). C and N were given in units g g-1 and stable isotopes were given as δ13C and δ15N for stable isotopes of C and N, respectively. Raw data C, N and stable isotope data were calibrated with certified standard and blank effects were corrected with the ilokeirms package (Teickner & Knorr, 2024). Using Fourier Transform Mid-Infrared Spectroscopy (FT-MIR) (Agilent Cary 670 FTIR spectromter, Agilent Technologies, Santa Clara, Ca, USA) humification indices (HI) were determined. Spectra were recorded from 600 cm-1 to 4000 cm-1 with a resolution of 2 cm-1 and baselines corrected with the ir package (Teickner, 2025) to estimate relative peack heights. The HI (no unit) for each sample was calculated by taking the ratio of intensities at 1630 cm-1 to the intensities at 1090 cm-1. Bulk densities (g cm-3) were estimated from FT-MIR data (Teickner et al., in preparation).

Geochemical parameters in peat depth profiles from ombrotrophic bogs in North and Central Europe. Pichlmaier Moor, Austria

This dataset contains geochemical variables measured in six depth profiles from ombrotrophic peatlands in North and Central Europe. Peat cores were taken during the spring and summer of 2022 from Amtsvenn (AV1), Germany; Drebbersches Moor (DM1), Germany; Fochteloër Veen (FV1), the Netherlands; Bagno Kusowo (KR1), Poland; Pichlmaier Moor (PI1), Austria and Pürgschachen Moor (PM1), Austria. The cores AV1, DM1 and KR1 were taken using a Wardenaar sampler (Royal Eijkelkamp, Giesbeek, the Netherlands) and had diameter of 10 cm. The cores FV1, PM1 and PI1 had an 8 cm diameter and were obtained using an Instorf sampler (Royal Eijkelkamp, Giesbeek, the Netherlands). The cores FV1, DM1 and KR1 were 100 cm, core AV1 was 95 cm, core PI1 was 85 cm and core PM1 was 200 cm. The cores were subsampeled in 1 cm (AV1, DM1, KR1, FV1) and 2 cm (PI1, PM1) sections. The subsamples were milled after freeze drying in a ballmill using tungen carbide accesoires. X-Ray Fluorescence (WD-XRF; ZSX Primus II, Rigaku, Tokyo, Japan) was used to determine Al (μg g-1), As (μg g-1), Ba (μg g-1), Br (μg g-1), Ca (g g-1), Cl (μg g-1), Cr (μg g-1), Cu (μg g-1), Fe (g g-1), K (g g-1), Mg (μg g-1), Mn (μg g-1), Na (μg g-1), P (μg g-1), Pb (μg g-1), Rb (μg g-1), S (μg g-1), Si (μg g-1), Sr (μg g-1), Ti (μg g-1) and Zn (μg g-1). These data were processed and calibrated using the iloekxrf package (Teickner & Knorr, 2024) in R. C, N and their stable isotopes were determined using an elemental analyser linked to an isotope ratio mass spectrometer (EA-3000, Eurovector, Pavia, Italy & Nu Horizon, Nu Instruments, Wrexham, UK). C and N were given in units g g-1 and stable isotopes were given as δ13C and δ15N for stable isotopes of C and N, respectively. Raw data C, N and stable isotope data were calibrated with certified standard and blank effects were corrected with the ilokeirms package (Teickner & Knorr, 2024). Using Fourier Transform Mid-Infrared Spectroscopy (FT-MIR) (Agilent Cary 670 FTIR spectromter, Agilent Technologies, Santa Clara, Ca, USA) humification indices (HI) were determined. Spectra were recorded from 600 cm-1 to 4000 cm-1 with a resolution of 2 cm-1 and baselines corrected with the ir package (Teickner, 2025) to estimate relative peack heights. The HI (no unit) for each sample was calculated by taking the ratio of intensities at 1630 cm-1 to the intensities at 1090 cm-1. Bulk densities (g cm-3) were estimated from FT-MIR data (Teickner et al., in preparation).

Geochemical parameters in peat depth profiles from ombrotrophic bogs in North and Central Europe. Pürgschachen Moor, Austria

This dataset contains geochemical variables measured in six depth profiles from ombrotrophic peatlands in North and Central Europe. Peat cores were taken during the spring and summer of 2022 from Amtsvenn (AV1), Germany; Drebbersches Moor (DM1), Germany; Fochteloër Veen (FV1), the Netherlands; Bagno Kusowo (KR1), Poland; Pichlmaier Moor (PI1), Austria and Pürgschachen Moor (PM1), Austria. The cores AV1, DM1 and KR1 were taken using a Wardenaar sampler (Royal Eijkelkamp, Giesbeek, the Netherlands) and had diameter of 10 cm. The cores FV1, PM1 and PI1 had an 8 cm diameter and were obtained using an Instorf sampler (Royal Eijkelkamp, Giesbeek, the Netherlands). The cores FV1, DM1 and KR1 were 100 cm, core AV1 was 95 cm, core PI1 was 85 cm and core PM1 was 200 cm. The cores were subsampeled in 1 cm (AV1, DM1, KR1, FV1) and 2 cm (PI1, PM1) sections. The subsamples were milled after freeze drying in a ballmill using tungen carbide accesoires. X-Ray Fluorescence (WD-XRF; ZSX Primus II, Rigaku, Tokyo, Japan) was used to determine Al (μg g-1), As (μg g-1), Ba (μg g-1), Br (μg g-1), Ca (g g-1), Cl (μg g-1), Cr (μg g-1), Cu (μg g-1), Fe (g g-1), K (g g-1), Mg (μg g-1), Mn (μg g-1), Na (μg g-1), P (μg g-1), Pb (μg g-1), Rb (μg g-1), S (μg g-1), Si (μg g-1), Sr (μg g-1), Ti (μg g-1) and Zn (μg g-1). These data were processed and calibrated using the iloekxrf package (Teickner & Knorr, 2024) in R. C, N and their stable isotopes were determined using an elemental analyser linked to an isotope ratio mass spectrometer (EA-3000, Eurovector, Pavia, Italy & Nu Horizon, Nu Instruments, Wrexham, UK). C and N were given in units g g-1 and stable isotopes were given as δ13C and δ15N for stable isotopes of C and N, respectively. Raw data C, N and stable isotope data were calibrated with certified standard and blank effects were corrected with the ilokeirms package (Teickner & Knorr, 2024). Using Fourier Transform Mid-Infrared Spectroscopy (FT-MIR) (Agilent Cary 670 FTIR spectromter, Agilent Technologies, Santa Clara, Ca, USA) humification indices (HI) were determined. Spectra were recorded from 600 cm-1 to 4000 cm-1 with a resolution of 2 cm-1 and baselines corrected with the ir package (Teickner, 2025) to estimate relative peack heights. The HI (no unit) for each sample was calculated by taking the ratio of intensities at 1630 cm-1 to the intensities at 1090 cm-1. Bulk densities (g cm-3) were estimated from FT-MIR data (Teickner et al., in preparation).

Schwerpunktprogramm (SPP) 1315: Biogeochemische Grenzflächen in Böden; Biogeochemical Interfaces in Soil, Importance of soil organic carbon and mineral particle size fractions for the fate of soil supplied organic chemicals and their microbial transformations

The biogeochemical interface (BGI) in this project is defined as the organo-mineral surface of soil particles colonized by microorganisms. In the preceding project it was demonstrated that the different soil particle size fractions were associated with specifically structured microbial communities, a characteristic amount of soil organic carbon, and a specific capacity for adsorption of the organic chemicals phenol and 2,4-dichlorophenol, respectively. While the diversity of the microbial community was responsive to fertilization-determined additional organic soil carbon in the larger particle size fractions, it was unaffected in clay. Stable isotope probing with 13C-labelled phenol and 2,4-dichlorophenol revealed that the soil organic carbon in the BGIs also affected the diversity of microorganisms involved in the degradation of these chemicals. All these results are yet only based on studying one soil with three organic carbon variants (Bad Lauchstädt) and only two organic compounds. The objective of this 2nd phase project is to apply the innovative technology developed in the 1st phase for studying the BGI processes with soil organic carbon variants from another soil (Ultuna, SPP 1315 site) and with the chiralic anilide Fungicide metalaxyl as an additional compound. This 2nd phase SPP 1315 project will also, in a collaborative effort with two other SPP 1315 partners, investigate (1) the importance of BGIs for the entantio-selective degradation of metalaxyl and (2) the role of soil microorganisms in the formation of bound residues, respectively. Furthermore, the project will utilize stable isotope probing and next-generation DNA sequencing to link the structural and functional diversity of the microbial communities responsible for metabolism of organic chemicals in the different BGIs determined by particle size fractions and soil organic carbon variants.

Social TrAnsformation of the BuiLding sEctor: Sozialgerechte Transformation des Mehrfamilienhausbestands hin zur Klimaneutralität mit Reallaborcharakter, Teilprojekt: Umsetzung einer versorgungssicheren, klimagerechten und wirtschaftlich tragbaren Energieversorgung in einem Mehrfamilienhaus

Im Rahmen des Projekts STABLE soll die Sanierung eines Mehrfamilienhauses (MFH) wissenschaftlich begleitet werden, wobei eine sozialgerechte Klimaneutralität oberste Prämisse ist. Das Projektkonsortium bringt die notwendigen Expert:innen aus Wissenschaft und Praxis an einen Tisch und schafft somit einen Verfahrensrahmen für die gesellschaftlich akzeptierte Energiewende im Gebäudebereich. Die Untersuchung aller relevanten Akteur:innen stellt sicher, dass die Transformation im Sinne der Gesellschaft stattfindet, was den langfristigen Erfolg des Konzepts sichert. Das Projekt umfasst sowohl die Konzeptionierung eines klimaneutralen Energiesystems für ein existierendes MFH als auch dessen Umsetzung und nachträgliche Begleitung. Damit ermöglicht das Projekt die ganzheitliche Untersuchung des Energiesystems auf der einen Seite und der relevanten Akteur:innen auf der anderen Seite. Für relevante Akteur:innen werden partizipative Methodiken angewandt, um die Energiewende für alle erlebbar zu machen, Bewohner:innen einzubinden und Interessenskonflikte sichtbar zu machen. Die Begleitung der Umsetzung garantiert, dass die zur sozialverträglichen Transformation des Gebäudebestandes existierenden Hürden erkannt sowie Lösungsstrategien entwickelt werden. Zudem wird durch den Dialog mit allen relevanten Akteur:innen angestrebt, dass ein Drehbuch die Erfahrungen aus den Beteiligungsprozessen und innovativen Partizipationsformaten für Sanierungsprojekte anderer Gebäudetypen übertragbar macht.

Optimization of a Method for the Isolation of Chloroplasts from Fresh Plant Material for the Development of a Bioassay Test for the Determination of Pesticides in Water

Bio-assays are increasingly used in supplement to classical analyses to determine the effect of contamination of waters with herbicides, some of which have been shown to be able to determine herbicides within the limits in compliance with EC-ordonance for drinking water. Preliminary work carried out at the University of Bonn has demonstrated that contamination of different water systems can be identified using inhibition of the light dependent production of oxygen by chloroplasts. Further experiments at IRMM have shown a potential to transfer membrane systems of chloroplasts into stable powder that can be used to carry out such bio-assays. Results: A method has been developed tor the isolation and breakage ot chloroplasts that allow freeze drying of the thylakoid membranes. The photosynthetic activity of the lyophilized material was maintained to 86 - 95 per cent. This powder can be stored for over five month without loss of activity.

Titanium stable isotope compositions of Neoarchean tonalite-trondhjemite-granodiorite (TTG) suites from the Eastern Goldfields Superterrane, Yilgarn Craton

We report the titanium (Ti) stable isotope compositions (δ49Ti) of Neoarchean (ca. 2700-2650 Ma) tonalite-trondhjemite-granodiorite (TTG) suites from the Eastern Goldfields Superterrane, Yilgarn Craton. Samples were selected to cover the full range of trace element compositions exhibited by TTGs, and are primarily from the Kalgoorlie-Kambalda region of the Kalgoorlie Terrane. Ti stable isotope compositions were measured using multicollector inductively coupled plasma mass spectrometry (MC-ICP-MS) at the Cardiff Earth Laboratory for Trace Element and Isotope Chemistry (CELTIC), Cardiff University. The Ti isotope compositions of these samples (file: 2025-009_Spencer-et-al_Ti-Isotope-Data.xlsx) are presented alongside a compilation of their major and trace element concentrations (file: 2025-009_Spencer-et-al_Compiled-Isotope-Major-Trace-Element-Data.xlsx) taken from the Western Australian Geochemistry Database (WACHEM). Most TTG samples have δ49Ti values between 0.2 to 0.6‰ that increase with SiO2 content, while two highly evolved TTGs have δ49Ti > 1‰. At SiO2 ≈ 70 wt% the different TTG geochemical groups display distinct Ti isotope compositions.

Field parameters and biochemical soil properties from NEP 1, NEP 2, NEP 3, Nördlingen, southern Germany

Soil physical-biogeochemical analyses were carried out on profiles NEP1, NEP2 and NEP3. Soil TC and TN were determined by CNS analysis, and total organic carbon (TOC) was determined by the difference between total inorganic carbon (TIC) and TC. Carbonate (CaCO₃) content was measured volumetrically using a Calcimeter and on air-dried, sieved (< 2 mm) and ground (ball mill) samples. The pH-values were measured on samples of profiles NEP1, NEP2, NEP3, which had less than 2% CaCO₃ content. Stable isotope ratios of δ¹³C and δ¹⁵N were analysed for the differentiation of C3 and C4 plants and the cultivation of legumes. The analyses were performed on air-dried, sieved (< 2mm) and ground (ball mill) samples. For ¹³C analysis, the soil samples were decarbonised with 10% HCl. In the field, separate samples were collected for the NEP1 and NEP2 profiles (28 samples in total) for analysis of urease activity and microbial biomass carbon (Cmic). Samples were stored at -18°C. Urease activity (enzyme analysis) is used to provide information on the input of urea and animal excrement. The mutual relationship between urease and Cmic was used to show and understand the past and present input of urea into the soil.

Agricultural And Aquaculture Facilities / Tierhaltungs- und Aufzuchtanlagen in Brandenburg

Der Datensatz Agricultural And Aquaculture Facilities / Tierhaltungs- und Aufzuchtanlagen in Brandenburg ist die Datengrundlage der interoperablen INSPIRE-Darstellungs- (WMS) und Downloaddienste (WFS): Tierhaltungsanlagen nach BImSchG in Brandenburg - Interoperabler INSPIRE View-Service (WMS-AF-TIERE) Tierhaltungsanlagen nach BImSchG in Brandenburg - Interoperabler INSPIRE Download-Service (WFS-AF-TIERE) Der Datenbestand beinhaltet die Punktdaten zu den betriebenen Tierhaltungsanlagen aus dem Anlageninformationssystem LIS-A. Die Angaben zu den Anlagen enthalten jeweils den Standort und die genehmigte Leistung. Dabei erfolgte eine sog. Schematransformation und Belegung der INSPIRE-relevanten Attribute. Der Datensatz Agricultural And Aquaculture Facilities / Tierhaltungs- und Aufzuchtanlagen in Brandenburg ist die Datengrundlage der interoperablen INSPIRE-Darstellungs- (WMS) und Downloaddienste (WFS): Tierhaltungsanlagen nach BImSchG in Brandenburg - Interoperabler INSPIRE View-Service (WMS-AF-TIERE) Tierhaltungsanlagen nach BImSchG in Brandenburg - Interoperabler INSPIRE Download-Service (WFS-AF-TIERE) Der Datenbestand beinhaltet die Punktdaten zu den betriebenen Tierhaltungsanlagen aus dem Anlageninformationssystem LIS-A. Die Angaben zu den Anlagen enthalten jeweils den Standort und die genehmigte Leistung. Dabei erfolgte eine sog. Schematransformation und Belegung der INSPIRE-relevanten Attribute. Der Datensatz Agricultural And Aquaculture Facilities / Tierhaltungs- und Aufzuchtanlagen in Brandenburg ist die Datengrundlage der interoperablen INSPIRE-Darstellungs- (WMS) und Downloaddienste (WFS): Tierhaltungsanlagen nach BImSchG in Brandenburg - Interoperabler INSPIRE View-Service (WMS-AF-TIERE) Tierhaltungsanlagen nach BImSchG in Brandenburg - Interoperabler INSPIRE Download-Service (WFS-AF-TIERE) Der Datenbestand beinhaltet die Punktdaten zu den betriebenen Tierhaltungsanlagen aus dem Anlageninformationssystem LIS-A. Die Angaben zu den Anlagen enthalten jeweils den Standort und die genehmigte Leistung. Dabei erfolgte eine sog. Schematransformation und Belegung der INSPIRE-relevanten Attribute.

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