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Korrosionsempfindliche Dosimetermaterialien zur Überwachung der Umweltbedingungen an Kulturgütern

Die einzelnen Belastungsfaktoren von Kulturgütern können durch apparativ aufwendige und kostenintensive Einzelmessungen mit Hilfe der modernen Analytik genau bestimmt werden. Mit den sogenannten Glassensoren wurde am Fraunhofer-Institut für Silicatforschung (ISC) eine elegante und zerstörungsfreie Methode entwickelt, die ohne aufwendige Messungen der einzelnen Parameter die auftretenden Gesamtbelastungen über einen längeren Zeitraum hinweg registrieren kann. Die Verwendung von sensibilisierten Glasflächen als Dosimetermaterial wurde für den bisherigen Anwendungsbereich ausgeschöpft. Ziel dieses Vorhabens ist es, neue korrosionsempfindliche Materialien und Komponenten herzustellen und für den prinzipiellen Einsatz zur Überwachung der Umweltbedingungen an Kulturgütern zu prüfen. Zum einen sollen Granulate der bisherigen Glasmaterialien mit unterschiedlicher Körnung in eine NIR-transparente Trägermatrix aus SiO2-Aerogel eingebracht werden. Zum anderen bietet sich die Modifizierung der inneren Oberfläche von SiO2-Aerogelen an, die dann selbst als detektionsaktive Medien fungieren können. Ein weiterer Syntheseweg soll so gewählt werden, dass Aerogel- oder Xerogelschichten ohne überkritische Trocknung auf Glas als Trägermaterial hergestellt werden. In jedem Fall muss der korrosive Einfluss bestimmter Umweltfaktoren (Feuchte, Temperatur, Schadgase) in einem Expositionsprogramm in Klimakammern, zunächst durch Variation einzelner Parameter und schließlich durch deren Kombination systematisch charakterisiert werden. Nach Abschluss dieser Labortestphase können - bei Projektende - Expositionsprogramme in Museen verwirklicht werden.

Updated global compilation of coccolithophore calcification measurements from unperturbed water samples including ancillary data

This database expands the Poulton et al., 2018 (doi:10.1594/PANGAEA.888182) database of pelagic calcium carbonate (CP) rate measurements from isotopic tracer uptake in incubated discrete water samples, as discussed in Daniels et al., 2018 (doi:10.5194/essd-10-1859-2018), and accompanies Marsh et al. (in prep.). The database now includes more CP (new data n = 400; complete database n = 3165), net primary production rate (PP) (new data n = 399; complete database n = 3150), total coccolithophore cell counts (new data n = 240; complete database n = 1512), and Emiliania huxleyi cell counts (new data n = 27; complete database n = 612). This expanded database maintains the record of data, including the principal investigator, expedition, OS region, doi reference (where available), collection date and year, sample ID, latitude, longitude, sampling and light depth, and method of measuring CP. We further expand the Poulton et al. (2018) data collection by including ancillary and environmental data, including: optical depth (OD, n = 3165), pHtotal (hereinafter referred to as pHT, n = 398), temperature (n = 1160), salinity (n = 1161), and the concentrations of chlorophyll a (n = 1363), NOx (NO3 or the sum of NO3 + NO2, n = 1161), silicic acid (Si(OH)4, n= 1156), phosphate (PO4, n = 1232), dissolved inorganic carbon (DIC, n = 318), total alkalinity (TA, n = 307), bicarbonate ion concentration (n = 349), and carbonate ion concentration (n = 352). All data was matched to CP, sample bottle identifiers (Niskin bottle numbers), and/or sampling depth values. This global database (81 °N - 64 °S, 132 °E - 174 °W) now covers expeditions and upper ocean measurements (0 - 193 m) from 1989 to 2024. Global in-situ geolocated data spanning time is valuable for modelling, satellite algorithms, and capturing calcium carbonate production in the global ocean. This expanded database, including the environmental, nutrient, chlorophyll a, and carbonate chemistry data, also allows for analysis of factors influencing calcium carbonate production on a global scale. This data amalgamation contributes to understanding the biogeochemistry of the oceans, global carbon cycle, and ocean acidification.

Forschergruppe (FOR) 1525: INUIT - Ice Nuclei research UnIT, Heterogende Eisnukleation ausgelöst durch poröse Materialien

Die Nukleation von Eispartikeln spielt eine wichtige Rolle bei der Wolken- und Niederschlagsbildung, mit Konsequenten für die atmosphärische Chemie, die Wolkenphysik und das Erdklima. Für eine Quantifizierung und Vorhersage des Einflusses von Wolken in Wettervorhersage- und Klimamodellen muss die Bildung von Eispartikeln daher in einer realistischen Art und Weise beschrieben werden. Einer der wichtigen Bildungsmechanismen ist dabei die heterogene Eisnukleation im Immersionsmodus, bei dem Eis an der Oberfläche eines in einem wässrigen Tröpfchen suspendierten Eiskeims - zum Beispiel eines Mineralstaub- Partikels - gebildet wird. Wir werden im Rahmen dieses Forschungsprojekts zahlreiche Gefrierexperimente im Immersionsmodus durchführen. So werden eine Reihe verschiedener, als Aerosolpartikel in der Atmosphäre vorkommende Materialien auf ihre Eisnukleationseigenschaften hin untersucht werden. Insbesondere sollen hier die Temperatur- und Zeitabhängigkeit der von diesen Materialien ausgelösten Eisnukleation quantifiziert werden. Dabei werden wir spezielles Augenmerk auf die systematische Untersuchung der von porösen Materialien ausgelösten Eisnukleation legen. Es sollen sowohl synthetische Materialien wie beispielsweise mesoporöse Silikate untersucht werden, als auch natürlich vorkommende Materialien wie etwa mikroporöse Zeolithe.

Whole-rock chemical analyses from the Heldburg dyke swarm

In the project "Geochemistry and geochronology of the Heldburg dyke swarm, Central European Volcanic Province" we conducted geochemical and geochronological investigations on mafic dykes and former magma chambers of the Heldburg dyke swarm. The latter is part of the Central European Volcanic Province and positioned in the South of Thuringia and the North of Bavaria (Germany). It consists of several hundred mafic NNE-SSW striking dykes with an usual thickness of < 1m and few former magma chambers. All of these have an atypical position within the Central European Volcanic Province located away from Hercynian massifs and major rift axes and were hitherto poorly investigated. In general, 10 different locations of the Heldburg dyke swarm were sampled for whole-rock analyses and 4 different locations were chosen for determining their apatite and zircon ages. The fieldwork was conducted between March 2022 and December 2023. The analytical work was done between June 2022 and April 2024 at the Department of Geodynamics and Geomaterials Research, University of Würzburg (samples preparation, X-ray fluorescence), at the GeoZentrum Nordbayern, University of Erlangen (trace element contents, LA-ICP-MS) and at FIERCE (Frankfurt Isotope & Element Research Center), Goethe University Frankfurt (apatite and zircon ages, LA-ICP-MS). Here, we present the full dataset of 55 whole-rock chemical analyses (X-ray fluorescence, LA-ICP-MS) from ten locations of the Heldburg dyke swarm.

KOSMOS 2023 Helgoland mesocosm study on ocean alkalinity enhancement: dissolved inorganic nutrients, chlorophyll a and suspended particulate organic matter

We conducted a mesocosm study to investigate ecosystem responses to ocean alkalinity enhancement (OAE) in the temperate waters of the German North Sea on Helgoland in spring 2023. We simulated non-CO2-equilibrated OAE via calcium hydroxide through the addition of calcium chloride and sodium hydroxide. Twelve 6 m³ mesocosms were used to simulate two scenarios: in six mesocosms we established a gradient of added alkalinity from 0 to 1250 µmol/kg in increments of 250 µmol/kg, simulating immediate (imm) dilution of alkalised waters. For the second set of six mesocosms, alkalinity was added only to the top 1 m of each mesocosm, doubling the target added alkalinity. The top layer was mixed with the untreated bottom layer after 48 hours, simulating delayed dilution of alkalised waters (del) and ultimately leading to the same alkalinity gradient as the immediate dilution treatment. This data contains water column biogeochemical variables, including dissolved inorganic nutrient concentrations (µmol/L), chlorophyll a concentrations (µg/L) and suspended particulate matter (biogenic silica, particulate organic carbon, nitrogen and phosphate; µmol/L). Nutrients, particulate organic phosphate and biogenic silica were measured spectrophotometrically (Unicam UV 300, Thermo Spectronic, USA). High-performance liquid chromatography (Thermo Scientific HPLC Ultimate 3000) was performed for chlorophyll a determination and particulate organic carbon and nitrogen were measured using an elemental analyser (Flash EA, Thermo Fisher).

Elementkarte der Digitalen Lithogeochemischen Karte von Bayern 1:25.000 (dLGK25) - Siliziumdioxid (P90)

Die Elementkarte stellt die räumliche Verteilung der klassifizierten Gehalte des 90. Perzentils von Siliziumdioxid (in Gew.-%) innerhalb der 184 geochemischen Gesteinseinheiten in Bayern dar. In die Auswertung gehen dabei nur die Daten der ersten (von maximal drei) Lithologien einer geochemischen Gesteinseinheit ein. Für Informationen im Hinblick auf die Auswertung der Daten sowie auf die kartenmäßige Darstellung wird auf die Metadaten der digitalen Lithogeochemischen Karte 1:25 000 von Bayern (dLGK25) verwiesen.

Elementkarte der Digitalen Lithogeochemischen Karte von Bayern 1:25.000 (dLGK25) - Siliziumdioxid (P50)

Die Elementkarte stellt die räumliche Verteilung der klassifizierten Gehalte des 50. Perzentils von Siliziumdioxid (in Gew.-%) innerhalb der 184 geochemischen Gesteinseinheiten in Bayern dar. In die Auswertung gehen dabei nur die Daten der ersten (von maximal drei) Lithologien einer geochemischen Gesteinseinheit ein. Für Informationen im Hinblick auf die Auswertung der Daten sowie auf die kartenmäßige Darstellung wird auf die Metadaten der digitalen Lithogeochemischen Karte 1:25 000 von Bayern (dLGK25) verwiesen.

Pore-water pH, H2S, Cl-, SO42-, SiO2, NO2-, PO43-, NH4+, NO3-, major and trace element data from MUC cores taken during RV HEINCKE cruises HE575 and HE595 in the Helgoland Mud Area, German Bight

This dataset includes downcore measurements of pH values, H2S, Cl-, SO42-, SiO2, NO2-, PO43-, NH4+, NO3-, As, Ba, Ca, Cu, Fe, K, Li, Mg, Mn, Mo, P, Si and Sr concentrations for sediment cores retrieved using multi-corer sampling during RV Heincke expeditions HE575 and HE595 in 2021 and 2022, respectively. The samples were collected in the framework of the Project APOC (Anthropogenic impacts on particulate organic carbon cycling in the North Sea). All measurements were performed in the laboratories of the Alfred Wegener Institute (AWI) in Bremerhaven, Germany, except pH values, which were determined onboard the research vessel.

Concentrations and loadings of fatty acids in surface sediments of Helgoland Mud Area in the North Sea

Surface sediment were extracted 4 times by ultrasonication with dichloromethane: methanol (9:1, v/v) for 15 min for FAs and alkanes. For quantification of FAs and alkanes, known amounts of 19-methylarachidic acid and squalane were added as internal standards prior to extraction. Supernatants from each extraction were obtained by centrifugation and combined. The total lipid extracts were concentrated and evaporated under a nitrogen stream. The total lipid extracts were saponified for 2 h at 80 °C with 1 mL of KOH (0.1 M) in methanol: H2O (9:1, v/v). After saponification, the neutral fractions were liquid-liquid extracted with n-hexane and alkanes were eluted from the neutral fractions by silica gel column chromatography with n-hexane. The remaining KOH solution was acidified to pH 1, from which FA were liquid-liquid extracted into dichloromethane. The extracted and dried FAs were converted to methyl ester derivatives (FAMEs) in methanol: HCl (95:5, v/v) at 60 °C for 12 h. After methylation, the FAME fraction was further purified by silica gel column chromatography using dichloromethane: hexane (2:1, v/v) to remove residual polar compounds. FAMEs and alkanes were analyzed on a 7890A gas chromatograph (GC) equipped with a DB-5MS fused silica capillary column (60 m, 250 µm, 0.25 µm) and a flame ionization detector (FID). Peak areas were determined by integrating the respective peaks and concentrations were calculated against the internal standards. FAME contents were subsequently corrected for the derivative methyl carbon to determine FA contents. FAs and alkanes were normalized to OC content.

KOSMOS 2023 Helgoland mesocosm study on ocean alkalinity enhancement: sediment trap particle flux data and water column biogeochemistry

The data presented herein originates from a mesocosm study conducted as part of the BMBF CDRmare, Retake project (grant agreement no. 03F0895A), aimed at investigating the ecological ramifications of ocean alkalinity enhancement (OAE). Twelve mesocosms were deployed in Helgoland South Harbor, Germany, and systematically sampled using integrated water samplers over the period spanning from March 12th to April 20th, 2023. Six alkalinity levels under two dilution scenarios were established to differentiate between localized and uniform OAE additions. Alkalinity was increased stepwise to ΔTAmax = 1250 μmol kg-1 (250 μmol TA kg-1 increments) using sodium hydroxide (NaOH) with calcium chloride (CaCl2) to simulate cation release during calcium-based mineral dissolution, causing strong carbonate chemistry perturbations (e.g., pHT > 9.25). The dataset encompasses a spectrum of sediment trap particle flux data, water column biogeochemistry including pigment variables, inorganic nutrients, carbonate chemistry parameters. The study and data set offer insights into impacts of alkalinity enhancement on marine ecosystems and their associated biogeochemistry.

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