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Timeseries of binned benthic stable carbon isotope from ODP Site 162-982,130-807 and ODP Site 162-982

This dataset contains C. wuellerstorfi stable carbon isotope values binned by marine isotope stage from ODP Site 162-807 and ODP Site 162-982 that span the last 4.5 million years (Feng et al. 2022; Venz et al. 1999, 2002; Hodell & Venz-Curtis 2006). This isotope gradient reflects the accumulation of respired and disequilibrium carbon in the deep Pacific ocean relative to the North Atlantic. Also included are binned probstack δ18O (Ahn et al., 2017) and ΔGMST (Clark et al., 2024) values for comparison to the binned stable carbon isotope values.

Water isotope time series (March 2020 - March 2021) of samples collected at A. P. Møller Skolen, Kleine Breite, Schlei

Time series of stable isotopes (δ2H and δ18O) were analyzed in water samples collected near the A. P. Møller Skolen, Schleswig (Kleine Breite, Schlei), in biweekly to monthly intervals between March 2020 and March 2021. Water was sampled with a pipette from ca. 0.5 m below water surface and directly transferred into a measurement vial. Isotope analysis was conducted at IGB Berlin, using a Picarro L2130-i cavity ring-down spectrometer. Water chemical parameters were measured in-situ with a modular WTW 3440 multiparameter devices and regularly calibrated conductivity cells (MPP 930 IDS, TetraCon® 925-P). The data give information about the seasonal isotope amplitude at the sampled locations and about spatial variability along the transects.

Seasonal water isotope values in eastern German lakes and rivers (Spree, Dahme, Elster and Mulde systems) in March, July, October 2022, and March 2023

Water isotopes (δ²H and δ¹⁸O) were analyzed in samples from lakes and rivers in eastern Germany. This sub-dataset is derived from water samples collected from lake and river shores. Seasonal samples were collected in March, July, October 2022, and in March 2023, with a plastic syringe from 20-50 cm depth below water surface and directly filtered and transferred into a measurement vial. Stable isotope analysis was conducted at IGB Berlin, using a Picarro L2130-i cavity ring-down spectrometer. Measurement uncertainty was quantified to <0.5 ‰ for δ²H and <0.2 ‰ for δ¹⁸O. Water chemical parameters were determined in-situ with a portable WTW-multiparameter probe. The data give information about the seasonal isotope amplitude at the sampled spots and about spatial isotope variability in different branches of the associated river systems.

Water isotope time series (March 2020 - March 2021) of samples collected in Kloster, Hiddensee

Time series of stable isotopes (δ2H and δ18O) were analyzed in water samples taken near the harbour of Kloster (Hiddensee), in biweekly to monthly intervals between March 2020 and March 2021. Water was sampled with a pipette from ca. 0.5 m below water surface and directly transferred into a measurement vial. Isotope analysis was conducted at IGB Berlin, using a Picarro L2130-i cavity ring-down spectrometer. Water chemical parameters were measured in-situ with WTW multiparameter measurement devices. The data give information about the seasonal isotope amplitude at the sampled locations and about spatial variability along the transects.

Immissions- und Strahlenschutz (GB 2)

• Überwachung der Radioaktivität in der Umwelt nach dem Strahlenschutzvorsorgegesetz für den Freistaat Sachsen • Überwachung der anlagenbezogenen Radioaktivität nach dem Atomgesetz am Forschungsstandort Rossendorf • Überwachung von Lebensmitteln (u. a. Amtshilfe für die Landesuntersuchungsanstalt für das Gesundheits- und Veterinärwesen Sachsen) • Betrieb der Radonberatungsstelle • Überwachung der anlagenbezogenen Radioaktivität nach der Verordnung zur Gewährleistung von Atomsicherheit und Strahlenschutz an den Standorten der Wismut GmbH • Überwachung der anlagenbezogenen Radioaktivität an den Altstandorten des Uranerzbergbaus • Aufsichtliche Messungen nach der Strahlenschutzverordnung inkl. Sicherheitstechnisch bedeutsame Ereignisse und Nukleare Nachsorge • Der Geschäftsbereich ist akkreditiert nach ISO 17025 für alle relevanten Prüfverfahren im Bereich Immission und Emission. Fachbereich 20 - Zentrale Aufgaben • Probenentnahmen und Feldmessungen (ohne Messungen und Probenentnahmen im Rahmen der Radonberatung) u. a. Probenentnahmen aus Fließgewässern, Messung der nuklidspezifischen Gammaortsdosisleistung • Organisation und Logistik für die von externen Probenehmern gewonnenen und dem Geschäftsbereich 2 zu übergebenden Proben. Betrieb der Landesdatenzentrale und der Datenbank zur Umweltradioaktivität im Freistaat Sachsen • Unterstützung der beiden Landesmessstellen bei der Einführung und Pflege radiochemischer Verfahren Fachbereiche 21, 22 - Erste und Zweite Landesmessstelle für Umweltradioaktivität Laboranalysen • nach dem Strahlenschutzvorsorgegesetz • zur Überwachung der Wismut-Standorte • zur Überwachung des Forschungsstandort Rossendorf • zur Überwachung der Altstandorte des Uranbergbaus • zur Lebensmittelüberwachung • zu den aufsichtlichen Kontrolltätigkeiten des Sächsischen Landesamtes für Umwelt, Landwirtschaft und Geologie und des Sächsischen Staatsministeriums für Umwelt und Landwirtschaft u. a. in den Medien Wasser, Boden, Luft, Nahrungs- und Futtermittel. Analysierte Parameter: u. a. gamma- und alphastrahlende Radionuklide (z. B. Cäsium-137, Cobalt-60, Kalium-40, Uran-238); Strontium-90; Radium-226 und Radium-228). Fachbereich 23 - Immissionsmessungen Kontinuierliche Überwachung der Luftqualität durch Betrieb des stationären Luftmessnetzes des Freistaates (Online-Betrieb von 30 stationären Messstationen mit Übergabe der Messdaten ins Internet): • Laufende Messung der Luftgüteparameter SO2, NOx, Ozon, Benzol, Toluol, Xylole, Schwebstaub, Ruß • Gewinnung meteorologischer Daten zur Einschätzung der Luftgüteparameter • Sammlung von Schwebstaub (PM 10- und PM 2,5-Fraktionen) und Sedimentationsstaub zur analytischen Bestimmung von Schwermetallen, polyzyklischen Kohlenwasserstoffen (PAK) und Ruß • Absicherung der Messdatenverarbeitung und Kommunikation • Betreiben einer Messnetzzentrale, Plausibilitätskontrolle der Daten und deren Übergabe an das Landesamt für Umwelt, Landwirtschaft und Geologie und an die Öffentlichkeit • Absicherung und Überwachung der vorgegebenen Qualitätsstandards bei den Messungen durch den Betrieb eines Referenz- und Kalibrierlabors • Sicherung der Verfügbarkeit aller Messdaten zu > 95% • Weiterentwicklung des Luftmessnetzes entsprechend den gesetzlichen Anforderungen • Betreuung eines Depositionsmessnetzes (Niederschlag) mit zehn Messstellen • Betrieb von drei verkehrsnahen Sondermessstellen an hoch belasteten Straßen • Durchführung von Sondermessungen mit Immissionsmesswagen und mobilen Containern • Betrieb von Partikelmesssystemen im Submikronbereich (Zählung ultrafeiner Partikel) in Dresden • Betrieb von Verkehrszähleinrichtungen und Übernahmen dieser Verkehrszähldaten sowie von Pegelmessstellen der Städte in den Datenbestand des Luftmessnetzes Fachbereich 24 - Emissionsmessungen, Referenz- und Kalibrierlabor Der Fachbereich befasst sich mit der Durchführung von Emissionsmessungen an ausgewählten Anlagen aus besonderem Anlass im Auftrag des LfULG. Beispiele: • Emissionsmessungen an Blockheizkraftwerken in der Landwirtschaft (Geruch, Stickoxide, Gesamtkohlenstoff und Formaldehyd). • Ermittlung der Stickstoff-Deposition aus Tierhaltungsanlagen für Geflügel und Rinder (Emissionsmessungen von Ammoniak, Lachgas, Methan, Wasser, Kohlendioxid, Feuchte, Temperatur und Luftströmung , Ammoniak-Immissionsmessung mit DOAS-Trassenmesssystem). • Untersuchung von Emissionen aus holzgefeuerten Kleinfeuerungsanlagen zur Abschätzung von Auswirkungen der novellierten 1. BImSchV. • Unterstützung des LfULG bei der Überwachung bekannt gegebener Messstellen nach § 26 BImSchG.

Pore water data of sediment incubation experiments under anoxic conditions

Enhanced mineral dissolution in the benthic environment is currently discussed as a potential technique for ocean alkalinity enhancement (OAE) to reduce atmospheric carbon dioxide (CO2) levels. This study explores how biogeochemical processes affect the dissolution of alkaline minerals in surface sediments during laboratory incubation experiments. These involved introducing dunite and calcite to organic-rich sediments from the Baltic Sea under controlled conditions in an anoxic to hypoxic environment. The sediment cores were incubated with Baltic Sea bottom water. Eight sediment cores were positioned vertically in a rack. Since the sediment surface was slightly oxidized by the bottom water (∼125 μmol l−1 upon recovery), the cores were left plugged on the top for 13 days to settle after recovery until the sediment surface was anoxic. To achieve chemical conditions that are expected in the natural system, 500l of retrieved sea water were degassed via bubbling with pure dinitrogen gas in batches of 100 l. Afterwards, between 50 and 60 l were transferred into an evacuated gas tight bag. After the transfer, pH and total alkalinity (TA) were measured to determine the dissolved inorganic carbon (DIC) of the water. Afterwards the DIC was increased via adding pure CO2 until a CO2 partial pressure (pCO2 ) of ∼2,300–∼3,300 μatm was established mimicking conditions prevailing in Boknis Eck during summer. Stirring heads were installed on the cores. To prevent the development of oxic conditions, it was ensured that as little gas phase as possible was left in the cores. Elimination of pelagic autotrophs, heterotrophs, and suspended particles was achieved by flushing the cores with modified bottom water for 2 days with a flow rate of 1.5 mml min−1. Afterwards, a continuous throughflow of 700 μl min−1 from the reservoir of modified bottom water was applied, leading to a residence time of ∼2.1 days inside the cores. For the experimental incubations, six cores received additions of alkaline materials, three with calcite (Cal1 - Cal3) and three cores with dunite (Dun1 - Dun3), leading to three replicates per treatment. Two control cores remained untreated (C1, C2). The amount of added substrate was based on the rain rate of particulate organic carbon observed in Boknis Eck (0.5 mmol cm−2 a−). The incubation lasted for 25 days. The volume of water in each core was determined at the end of the experiment via measuring the height of the water column after removing the stirring heads. At the end of the experiments, the bottom water was removed via suction and the cores were sliced for pore water analysis. The pore waters were recovered by centrifuging each respective sediment layer in 50 ml falcon tubes at 3000 rpm for 10 minutes. Afterwards, the supernatant water was transferred to polyethylene (PE) vials in an Ar-filled glove bag to minimize contact with oxygen. All samples were filtered through a 0.2 µm cellulose membrane filter and refrigerated in 25 ml ZinsserTM scintillation vials. TA samples (1 ml) were titrated with 0.02N HCl. For H2S, an aliquot of pore water was diluted. A 5 ml aliquot was frozen directly after the sampling procedure for later nutrient analysis. Nutrient measurements were performed either via manual photometric measurement (NH4) or using a Seal – AnalyticalTM QuAAtro autoanalyzer (PO43-). Samples for TA were analyzed directly after sampling by titration of 1 ml of bottom/pore water with 0.02N HCl. Titration was ended when a stable purple color appeared. During titration, the sample was degassed by continuous bubbling with nitrogen to remove any generated CO2 and H2S. The acid was standardized using an IAPSO seawater standard. Acidified sub-samples (30 μl suprapure HNO3- + 3 ml sample) were prepared for analyses of major and trace elements (Si, Na, K, Li, B, Mg, Ca, Sr, Mn, Ni and Fe) by inductively coupled plasma optical emission spectroscopy (ICP-OES, Varian 720-ES). For H2S, an aliquot of pore water was diluted with appropriate amounts of oxygen-free artificial seawater and the H2S was fixed by immediate addition of zinc acetate gelatin solution

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.

Pore-water DIC and δ13C-DIC data, as well as solid-phase porosity and TOC data from a MUC core from RV HEINCKE cruise HE595 at Tonne E3 in the Helgoland Mud Area, SE German Bight

This dataset includes downcore measurements of dissolved inorganic carbon (DIC) and its stable carbon isotopic composition (δ13C-DIC), as well as solid-phase porosities and total organic carbon (TOC) contents from a sediment core retrieved using multi-corer sampling during RV Heincke expedition HE595 in 2022. The samples were collected in the framework of the Project APOC (Anthropogenic impacts on particulate organic carbon cycling in the North Sea). DIC contents were determined in the laboratories of the Alfred Wegener Institute (AWI) in Bremerhaven, Germany. The δ13C-DIC data were produced at MARUM—Center for Marine Environmental Sciences, University of Bremen, Bremen, Germany. Solid-phase porosity data were produced in the laboratories of the Alfred Wegener Institute (AWI) in Bremerhaven, Germany. Total organic carbon contents were determined at the Faculty of Geosciences at the University of Bremen, Bremen, Germany.

Seasonal Dataset of DIC, δ13CDIC, DOC, δ13CDOC, pCO2(aq), FCO2 and Biogeochemical Parameters in the Danube River (2023–2024)

This dataset contains dissolved inorganic/organic carbon (DIC/DOC) concentrations, its stable isotope ratios (δ13CDIC/DOC), partial pressure of carbon dioxide in the water column pCO₂(aq) (pCO2(aq)) and area-integrated CO₂ emission rates derived from flux calculations (FCO2; g C d⁻¹), along with corresponding parameters (temperature, pH, calcium, bicarbonate) collected from the Danube River and its key tributaries during five seasonal sampling campaigns in 2023 and 2024. Water samples were collected using a weighted 2 L sampling bottle submerged 1–2 meters below the surface, with sampling conducted from the river center via bridges or passenger boats, and occasionally from the riverbank. In situ temperature measurements were taken with a multiparameter instrument (HQ40d, HACH™, Loveland, CO, USA). δ13ODIC/DOC was analyzed using a OI Analytical Aurora 1030W-IRMS. This dataset is providing valuable insights into carbon dynamics in a large river system and support investigations of biogeochemical cycling. It further can inform ecosystem management and conservation strategies under changing environmental conditions.

Pore water data of laboratory incubation experiments on enhanced benthic weathering in organic rich Baltic Sea sediments

Enhanced mineral dissolution in the benthic environment is currently discussed as a potential technique for ocean alkalinity enhancement (OAE) to reduce atmospheric carbon dioxide (CO2) levels. This study explores how biogeochemical processes affect the dissolution of alkaline minerals in surface sediments during laboratory incubation experiments (January - May 2022). These involved introducing dunite and calcite to organic-rich sediments from the Baltic Sea under controlled conditions in an oxic environment. The sediment cores were incubated with Baltic Sea bottom water. Eight sediment cores were placed in a rack in an upright position. The bottom water was carefully removed via suction and replaced with a known volume (1.5 l – 2.0 l) of filtered (0.2 µm) Baltic Sea bottom water in order to remove pelagic auto- and heterotrophs and suspended particles. The volume of water added depended on the height of sediment in each core which varied slightly due to the recovery method. After this procedure, a gaseous headspace of ca. 10 cm was left in each core. Furthermore, the cores were equipped with adjustable stirring heads that contained ports for inserting optodes to continuously record pH and oxygen (O2) concentrations in the overlying water. In order to prevent anoxic conditions developing, ambient air was bubbled into the water column. The water column in each core was slowly and continuously flushed with a constant throughflow of 40 µl min-1 from a single reservoir of bottom water. The residence time of the water inside the cores was thus about 4 to 5 weeks. At the end of the experiments, the bottom water was removed via suction and the cores were sliced for pore water analysis. The pore waters were recovered by centrifuging each respective sediment layer in 50 ml falcon tubes at 3000 rpm for 10 minutes. Afterwards, the supernatant water was transferred to polyethylene (PE) vials in an Ar-filled glove bag to minimize contact with oxygen. Samples for TA were analyzed directly after sampling by titration of 1 ml of bottom/pore water with 0.02N HCl. Titration was ended when a stable purple color appeared. During titration, the sample was degassed by continuous bubbling with nitrogen to remove any generated CO2 and H2S. The acid was standardized using an IAPSO seawater standard. Anion element concentrations (SO42-, Cl-, Br-) were determined using ion chromatography (IC, METROHM 761 Compact, conductivity mode). Acidified sub-samples (30 μl suprapure HNO3- + 3 ml sample) were prepared for analyses of major and trace elements (Si, Na, K, Li, B, Mg, Ca, Sr, Mn, Ni and Fe) by inductively coupled plasma optical emission spectroscopy (ICP-OES, Varian 720-ES). In addition to the parameters listed above, pore waters were analyzed for sulfite (H2S) and Fe2+. For the analysis of dissolved Fe2+ concentrations, sub-samples of 1 ml were taken within the glove bag, immediately stabilized with ascorbic acid and analyzed within 30 minutes after complexation with 20 μl of Ferrozin. For H2S, an aliquot of pore water was diluted with appropriate amounts of oxygen-free artificial seawater and the H2S was fixed by immediate addition of zinc acetate gelatin solution.

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