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.
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.
Climate change-driven deglaciation and erosion in high-latitude regions enhance the flux of terrigenous material to the coastal ocean. Newly exposed land surfaces left behind by retreating glaciers are covered by glacial till, which is rich in fine-grained minerals. Many of these minerals are undersaturated in seawater and thus prone to dissolution (i.e., seafloor weathering). Consequently, intensified erosion and mineral weathering may act as an additional CO₂ sink while supplying alkalinity to coastal waters. To evaluate this hypothesis, we carried out a sediment geochemical study in the southwestern Baltic Sea, where coastal erosion of glacial till is the dominant source of terrigenous material to offshore depocenters. We analyzed glacial till from coastal cliffs, sediments, and pore waters for major element composition using inductively coupled plasma optical emission spectroscopy and an elemental analyzer. Water samples were further analyzed for dissolved redox species and dissolved silica by photometry and ion chromatography. These data were then used to quantify mineral dissolution and precipitation processes and to assess their net effect on inorganic carbon cycling.
The 11.8 m-long composite sediment record from the hardwater lake of Sacrower See, located near the city of Potsdam (north-eastern Germany), has been characterised by a range of analytical techniques. These include magnetic susceptibility, chemical parameters (XRF core scanning, CNS analysis, biogenic silica) and stable isotopes (13C, 15N). The chronology covers the entire Holocene and the concluding Lateglacial (Alleröd, Younger Dryas) and is based on age-depth modelling using radiocarbon dates refined by the onset of the local varve chronology in 1870 CE (Lüder et al., 2006) and by the Laacher See Tephra, an isochrone dated to 13,000 cal. BP. It offers a detailed environmental reconstruction providing insights into depositional processes influenced by both natural climatic variations and human activities (Enters et al., 2009; Kirilova et al., 2009). The Lateglacial and Early Holocene are distinguished by the stabilisation of natural landscapes characterised by the presence of pine-birch (Alleröd) and mixed oak forests (Early Holocene). This development was interrupted by the climatic deterioration of the Younger Dryas, which resulted in a destabilisation of vegetation and increased natural soil erosion. It is evident that, for the first time around 5500 cal. BP, anthropogenic forest clearing became a factor, which subsequently led to increasing cultural soil erosion further accelerating during the Bronze Age (3600-3200 cal. BP), the Early Iron Age (2800-2600 cal. BP) and the Middle Ages (900-600 cal. BP). In the course of industrialisation since the 19th century, human impact underwent a transition from the destabilisation of soils to the phenomenon of eutrophication. This transition resulted in the occurrence of hypolimnetic anoxia, accompanied by the formation of carbonaceous varves.
Unraveling the role of the Southern Ocean's biological pump in regulating climate would be enhanced by the development of paleoceanographic proxies specific to carbon or silica cycling. Observations that the average size of valves of the diatom, Fragilariopsis kerguelensis, varies seasonally, with latitude, and over glacial-interglacial cycles in the Southern Ocean suggest that the valve size frequency distribution in sediments could be used to reconstruct aspects of paleoproductivity and silica cycling. We aim to develop this proxy by using culture, field and sediment samples to determine the exact controls on valve size frequency distributions, the most important of which is likely to be the frequency of auxospore formation within the population. The controls on auxospore formation are as yet unknown and both mating experiments in culture as well as in situ iron fertilization experiments are likely to unravel the mechanisms determining auxospore formation under both controlled and field conditions. The valve size frequency distribution can then be used to indicate the intensity of the environmental and/or biological conditions triggering auxospore formation.
The Jacupiranga carbonatite (Brazil) was investigated to better understand how modal proportions and mineral chemistry control the fO2 recorded by a natural carbonatite rock. Mineral compositions were determined using SEM-EDS, EPMA-WDS and Raman microspectroscopy building upon detailed petrography. Based on magnetite-ilmenite oxythermobarometry, rock-forming temperatures range from 505 to 732 °C, with a wide span of fO2 values (∆FMQ –1.21 to +4.56). In each sample, ilmenite grains and lamellae are distinguishable, with the latter recording higher temperature–fO2 conditions. Consistently, independently determined homogenization temperatures of apatite-hosted fluid inclusions show a similar range between 550 and 685 °C. From the wall-rock contact toward the carbonatite body, samples exhibit a decrease in the modal abundance of olivine, phlogopite, magnetite, ilmenite, and dolomite, alongside an increase in Mg-calcite. Over the same spatial gradient, temperature, fO2, and the magnesioferrite (in magnetite) and geikielite (in ilmenite) components decrease. During the antiskarn reaction, silica and mafic components (Mg, FeT, Al, and Ti) derived from the ultramafic wall-rock were incorporated into olivine, phlogopite, magnetite-ilmenite, and dolomite. Calcite-rich samples, which were less influenced by the wall-rock, preserved ephemeral alkali components of the carbonatite melts within burbankite. Apatite-hosted fluid inclusions represent coeval fluid modified by antiskarn reactions. Adjacent to equilibrium magnetite-ilmenite pairs, olivine and phlogopite exhibit high mg# (93–97 and 88–95, respectively). Despite the broad span of ∆FMQ values recorded by the oxide pairs, we found only a weak positive correlation between the recorded fO2 and mg#. Consequently, we suggest that the high mg# (>88–90) of carbonatitic olivine is primarily controlled by the low (<0.2) 〖K_D〗_(Fe^(2+)-Mg)^(olivine-carbonatite melt) (Fe2+/Mg exchange partition coefficient between olivine and the carbonatite melt) at crustal conditions. The exceptionally high mg# of olivine and phlogopite, compared to the adjacent dunite cumulates (mg# 84–88), combined with their negligible Ni and Cr contents, indicate an in situ antiskarn process. This study demonstrates that carbonatite systems can be characterized by dynamic redox conditions, spanning the range from Fe3O4 ̶ Fe2O3 to Fe2SiO4 ̶ Fe3O4 ̶ SiO2 during their evolution and emplacement.
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).
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.
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.
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