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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).

Seasonal (years 2020-2021) dynamics in pore water composition under impact of submarine groundwater discharge in front of a coastal peatland, southern Baltic Sea

The data set contains the results for the porewater composition of samples, collected from different (up to 11) depths (down to 4.5 mbsf) at two sites in front of the Hütelmoor, southern Baltic Sea. Porewater was under impact by submarine groundwater discharge and collected during 6 field campaigns in years 2020 and 2021 using permanent multi-port samplers. Stable isotope signatures (H, C, O, S), major, and trace element data are presented to characterize the mixture between the endmembers freshwater and the brackish surface water component, superimposed by benthic diagenesis.

CO2 degassing from karstic springs in Southern Germany

This study examines characteristics of dissolved inorganic carbon (DIC) and partial pressures of CO2 characteristics (pCO2) in the source springs and headwaters of four karstic watersheds, via dissolved inorganic carbon concentration and stable carbon isotope measurements. All four spring sources are located in Southern Germany and were measured for water chemistry and stable isotopes with nearby headwater stream points, which were located up to 100 m downstream of the discharge points. Seasonal sampling covered winter, spring, summer, and autumn in 2018.

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.

Immissions- und Emissionsmessungen von Bioaerosolen im Bereich von Geflügel- und Schweinestallungen (Luquasta) - Teilbereich HBLFA Raumberg-Gumpenstein

Bedeutung des Projekts für die Praxis: Die Daten sollen einen Hinweis darauf geben, ob die Maßnahmen in der Landwirtschaft im Luftreinhalteprogramm 2014 des Landes Steiermark eine Minimierung der Bioaerosol Konzentration in der Luft bewirken können. In einem Merkblatt werden Faktoren, die zur Minimierung der Konzentration luftgetragener Keime und Partikel führen, aufgeführt. Wenn zwischen Kontaminationsquellen und Anrainern eine Übertragung von Staub und seinen biologischen Bestandteilen bzw. Keim- und Staubemission weitgehend ausgeschlossen werden kann, sind normalerweise aus umweltmedizinischer Sicht Emissions-minderungsmaßnahmen nicht erforderlich. Mit den vorliegenden Ergebnissen besteht die Möglichkeit ein für die Steiermark und anderen Ländern gültiges Konzept mit regionalspezifischer Vorgehensweise zu erarbeiten. Zielsetzung: Die HBLFA Raumberg-Gumpenstein, Abt. Tierhaltungssysteme, Technik & Emissionen, Institut für Tier, Technik und Umwelt ist im gegenständlichen Projekt (genehmigter Antrag wurde durch die Medizinische Universität Graz gestellt, Nr. 101263/3) entscheidend an der Auswahl der Versuchsbetriebe beteiligt, sie stellt zum Teil die Kontakte zu den Betriebsleitern her, übernimmt in den einzelnen Messkampagnen die Emissionsmessungen an den Kaminöffnungen der Projektbetriebe und ist den gesamten Projektablauf (Planung der Messungen, regelmäßige Besprechungen, Diskussion der Auswertungsergebnisse, Erstellung des Abschlussberichtes) involviert. Des Weiteren werden an den jeweiligen Messtagen auf den Projektbetrieben der Status der Lüftungstechnik (Ansteuerungsleistung der Ventilatoren, Messung der Abluftgeschwindigkeit ...) sowie die Bedingungen im Stall und Tierbereich (Temperatur, Feuchte, Tiergewichte, Futtermittel, Einstreu ...) dokumentiert Das Ziel dieses Projekts besteht darin, den Istzustand der Emissionen und Immissionen von Bioaerosolen und Feinstaubpartikeln im Bereich von Tierhaltungsanlagen mit verschiedenen Messstrategien zu erheben. Für die Beurteilung der anlagenbezogenen Emissionen und Immissionen wird vergleichend die natürliche Hintergrundkonzentration der Bioaerosole und Feinstaubpartikel in der Umgebungsluft bestimmt. Es gilt festzustellen, ob die Keimkonzentrationen der Umgebungsluft aus der Stallluft resultieren. Die Leitparameter (Keime bzw. biogene Substanzen), welche in VDI 4250 Blatt 3 (2016) Richtlinie zur Emissions- und Immissionsbeurteilung herangezogen werden, werden auf ihre Adaptierbarkeit überprüft. Für die zukünftigen Bewertungen der Immissionen werden Ausbreitungsrechnungen durchgeführt, um die Fläche des Areals zu definieren, in dem ein neu zu errichtendes Stallgebäude für die Haltung von Nutztieren stehen soll. Die Daten aus der vorliegenden Studie werden mit den Ergebnissen und Bewertungen anderer EU Länder verglichen, um ein Konzept für eine Bewertungsgrundlage zu erstellen. (Text gekürzt)

T-LAB: Global Maps of the Thermal Lithosphere-Asthenosphere Boundary Derived from Shear-Wave Tomography Models and Mineral Physics Constraints

The lithosphere-asthenosphere boundary (LAB) marks the base of the Earth’s outer layer where heat is transferred primarily by conduction as compared to prevailing convective heat transport below. Spatial variations in LAB depth reveal the differential evolution of tectonic systems (e.g., rifts and orogens), thus enabling a better understanding of geodynamic processes. Further, the topography of the LAB exerts control on the coupling of the lithosphere to asthenospheric flow, modulating the distribution of present-day stresses and active deformation of the tectonic plates. We have derived global depth variations of the LAB from temperature-converted shear-wave tomography models assuming that the threshold temperature between conduction and mantle convection is 1300 °C. Shear-wave velocity in the mantle is controlled by both in situ pressure-temperature conditions and mineralogical rock composition. Therefore, our velocity-to-temperature conversion builds on a framework of rock physical properties generated through a Gibbs free energy minimization to determine thermodynamically stable phase and mineral assemblages throughout upper mantle pressure and temperature conditions. In this data publication, we provide thermal LAB depths corresponding to one European-scale and three global-scale tomography models. The data release includes (i) a data description file with information on the input tomographic models, the conversion method and spatial variations in LAB depth (illustrated); and (ii) four data files with LAB depth values spatially sampled according to the input tomography models.

Effect of diffusive/dispersive processes on stable isotope ratios of organic contaminants in aquifer systems

Groundwater contamination by organic compounds represents a widespread environmental problem. The heterogeneity of geological formations and the complexity of physical and biogeochemical subsurface processes, often hamper a quantitative characterization of contaminated aquifers. Compound specific stable isotope analysis (CSIA) has emerged as a novel approach to investigate contaminant transformation and to relate contaminant sources to downgradient contamination. This method generally assumes that only (bio)chemical transformations are associated with isotope effects. However, recent studies have revealed isotope fractionation of organic contaminants by physical processes, therefore pointing to the need of further research to determine the influence of both transport and reactive processes on the observed overall isotope fractionation. While the effect of gasphase diffusion on isotope ratios has been studied in detail, possible effects of aqueous phase diffusion and dispersion have received little attention so far.The goals of this study are to quantify carbon (13C/12C) and, for chlorinated compounds, chlorine (37Cl/35Cl) isotope fractionation during diffusive/dispersive transport of organic contaminants in groundwater and to determine its consequences for source allocation and assessment of reactive processes using isotopes. The proposed research is based on the combination of high-resolution experimental studies, both at the laboratory (i.e. zero-, one- and two-dimensional systems) and at the field scales, and solute transport modeling. The project combines the expertise in the field of contaminant transport with the expertise on isotope methods in contaminant hydrogeology.

Compilation of global Archean and Paleoproterozoic sanukitoid geochemical data

Sanukitoids, also referred to as high-Mg diorites, are a distinctive type of igneous rock from the late Archean-early Proterozoic, and are characterised by enrichment in both compatible elements (e.g. Mg, Ni, Cr) and incompatible elements (e.g. Ba, Sr, light rare earth elements). Their geochemistry is typically interpreted as recording petrogenesis of their parental magmas via interaction between mantle peridotite and recycled crust-derived component (e.g. metabasite melts, sediment melts, aqueous fluids), and is often considered to be "transitional" between that of Archean sodic tonalite-trondhjemite-granodiorite (TTG) suites and post-Archean potassic granites. This dataset presents a global compilation of all Archean-Paleoproterozoic rocks that have been described as "sanukitoid" in published literature, and consists of over 3600 individual samples. Whole rock major and trace element concentrations, radiogenic isotope compositions and stable isotope compositions are compiled in the dataset alongside reported magmatic ages of the samples. The dataset is provided both as an Excel workbook divided by craton (file: 2025-003_Spencer-et-al_Sanukitoid-Compilation.xlsx) and as a single CSV file (file: 2025-003_Spencer-et-al_Sanukitoid-Compilation.csv). Sanukitoid magmatism has been described on almost every Archean craton globally. Most reported sanukitoid magmatism occurred during the late Mesoarchean-Neoarchean (2.95 - 2.5 Ga), with another peak in sanukitoid magmatism in the mid-Paleoproterozoic (2.2 - 2.0 Ga). Older sanukitoid occurrences dating back to the Paleoarchean (>3.2 Ga) are also described in the literature.

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