ALBERT

Description: Nach der Übernahme des Territoriums des Klosters Grünhain durch die Wettiner im Jahr 1536 und der Verwaltungsreform durch Kurfürst Moritz wurde für den Bergbau am Emmler eine neue Bergordnung notwendig. Diese erließ der Oberhauptmann des (erz)gebirgischen Kreises, Heinrich von Gersdorff, in seiner Amtszeit zwischen 1547 und 1554.

Description: source

Description: Volcanogenic massive sulfide deposits may represent a significant future source of Te, which is a critical element important for the green energy transition. Tellurium is enriched in these settings by up to 10,000 times over its crustal abundance, indicating that fluids in sea-floor hydrothermal systems may transport and precipitate Te. The major element composition of these hydrothermal fluids is controlled by fluid-rock interaction and is well documented based on experimental, modeling, and natural studies; however, controls on Te mobility are still unknown. To better understand Te enrichment in this deposit type, numerical simulations of the mafic-hosted Vienna Woods and the felsic-hosted Fenway sea-floor vents in the Manus basin were performed to predict Te mobility in modern sea-floor hydrothermal vent fluids and Te deposition during sulfide formation. These simulations demonstrate that the mobility of Te in sea-floor hydrothermal systems is primarily controlled by fluid redox and temperature. Tellurium mobility is low in reduced hydrothermal fluids, whereas mobility of this metal is high at oxidized conditions at temperatures above 250°C. Numerical simulations of the reduced vent fluids of the mafic-hosted Vienna Woods site at the back-arc spreading center in the Manus basin yielded Te concentrations as low as 0.2 ppt. In contrast, the more oxidized model fluids of the felsic-hosted Fenway site located on Pual Ridge in the eastern Manus basin contain 50 ppt Te. The models suggest that Te enrichment in these systems reflects rock-buffer control on oxygen fugacity, rather than an enriched source of Te. In fact, the mafic volcanic rocks probably contain more Te than felsic volcanic rocks. The association of elevated Te contents in the felsic-hosted Fenway system likely reflects magmatic volatile input resulting in lower pH and higher Eh of the fluids. More generally, analysis of sulfide samples collected from modern sea-floor vent sites confirms that redox buffering by the host rocks is a first-order control on Te mobility in hydrothermal fluids. The Te content of sulfides from sea-floor hydrothermal vents hosted by basalt-dominated host rocks is generally lower than those of sulfides from vents located in felsic volcanic successions. Literature review suggests that this relationship also holds true for volcanogenic massive sulfides hosted in ancient volcanic successions. Results from reactive transport simulations further suggest that Te deposition during sulfide formation is primarily temperature controlled. Modeling shows that tellurium minerals are coprecipitated with other sulfides at high temperatures (275°–350°C), whereas Te deposition is distinctly lower at intermediate (150°–275°C) and low temperatures (100°–150°C). These predictions agree with geochemical analyses of sea-floor sulfides as Te broadly correlates positively with Cu and Au enrichment in felsic-hosted systems. The findings of this study provide an important baseline for future studies on the behavior of Te in hydrothermal systems and the processes controlling enrichment of this critical mineral in polymetallic sulfide ores.

Description: FS METEOR Expedition M201 VebVolc, 09.06. – 18.07.2024 | Reykjavik – Praia da Vitoria

Description: Ocean Alkalinization deliberately modifies the chemistry of the surface ocean to enhance the uptake of atmospheric CO2. Here we quantify, using idealized Earth system model (ESM) simulations, changes in carbon cycle feedbacks and in the seasonal cycle of the surface ocean carbonate system due to ocean alkalinization. We find that both, carbon-concentration and carbon climate feedback, are enhanced due to the increased sensitivity of the carbonate system to changes in atmospheric CO2 and changes in temperature. While the temperature effect, which decreases ocean carbon uptake, remains small in our model, the carbon concentration feedback enhances the uptake of carbon due to alkalinization by more than 20%. The seasonal cycle of air-sea CO2 fluxes is strongly enhanced due to an increased buffer capacity in an alkalinized ocean. This is independent of the seasonal cycle of pCO2, which is only slightly enhanced. The most significant change in the seasonality of the surface ocean carbonate system is an increased seasonal cycle of the aragonite saturation state, which has the potential to adversely affect ecosystem health.

Description: Marginal seas influenced by large rivers are characterized by complex hydrodynamic and organic matter cycling processes. However, the impacts of hydrodynamics on the composition and reactivity of particulate organic matter (POM) remain unclear. Here we conducted a comprehensive study on the bulk, molecular and biological properties of suspended POM in the Changjiang Estuary and adjacent area subjected to strong currents, eddies as well as typhoons during spring and autumn. D/L‐enantiomers of particulate amino acids (PAA) were analyzed to evaluate the bioreactivity of POM and quantify bacterial‐derived organic carbon. We found that POM bioavailability as indicated by carbon‐normalized yields of PAA (PAA‐C%) reflected the ecosystem productivity. Relatively high PAA‐C% values (20−35%) were observed in productive areas influenced by Changjiang River plume, cyclonic eddies and typhoons, likely related to the enhanced nutrient availability arising from hydrodynamic processes. In contrast, the oligotrophic Taiwan Warm Current‐influenced regions featured relatively low POM bioavailability (PAA‐C% 〈 10%) despite typhoons facilitating water mixing. The PAA‐C% values showed a significant positive correlation with extracellular enzyme activity, indicating that bioavailable POM can rapidly stimulate heterotrophic transformation. Hot spots of elevated bioavailable POM showed high contributions of bacterial organic carbon. A large portion (∼2/3) of bacterial organic carbon was present in the form of bacterial detritus, suggesting that patches of these biological hot spots represent important sites of carbon sequestration. Together, our findings indicate that fresh POM production is largely controlled by nutrient supply driven by hydrodynamic processes, with important implications for carbon sequestration in the dynamic ocean margins. Plain Language Summary Marginal seas are subject to complex hydrodynamic processes and play an important role in carbon sequestration. Disentangling the linkages between hydrodynamics and organic carbon reactivity and composition is crucial to understanding the regional carbon cycle. Here we collected suspended particulate organic matter (POM) in the Changjiang Estuary and adjacent coastal areas. Based on the biomarker D/L‐amino acids, we assessed the bioavailability of POM and quantified the organic carbon originating from bacteria. We found that high bioactivity of POM occurred in productive Changjiang River plume, cyclonic eddy, and typhoon influenced areas. These hydrodynamic processes appear to increase nutrient availability, therefore promoting phytoplankton growth. Bioavailable POM can rapidly stimulate heterotrophic activity and facilitate the transformation of algal‐derived organic carbon to bacterial detritus, thus contributing to carbon sequestration. Our findings suggest that the production of bioavailable POM is largely controlled by hydrodynamically driven nutrient supply. Key Points We use D/L‐amino acids to assess the bioreactivity and bacterial origins of particulate organic matter (POM) in the dynamic Changjiang Estuary and adjacent area High bioavailability of POM occurs in productive regions affected by Changjiang River plume, cyclonic eddies and typhoons Hot spots of bioavailable POM represent important sites for carbon sequestration

Description: The Gulf of St. Lawrence is increasingly affected by bottom water hypoxia; however, the timescales and pathways of deep water transport remain unclear. Here, we present results from the Deep Tracer Release eXperiment (TReX Deep), during which an inert SF 5 CF 3 tracer was released inshore of Cabot Strait at 279 m depth to investigate deep inflow transport and mixing rates. Dispersion was also assessed via neutrally-buoyant Swish floats. Our findings indicate that the tracer moves inland at 0.5 cm s −1 , with an effective lateral diffusivity of 2 × 10 2 m 2 s −1 over 1 year. Simplified 1D simulations suggest inflow water should reach the estuary head in 1.7 years, with the bulk arriving after 4.7 years. Basin-wide effective vertical diffusivity is around 10 −5 m 2 s −1 over 1 year; however, vertical diffusivity increases near the basin slopes, suggesting that turbulent boundary processes influence mixing. These results are compared to Lagrangian simulations in a regional 3D model to evaluate the capacity to model dispersion in the Gulf.

Description: The Western Tropical Atlantic Ocean (WTAO) is crucial for understanding CO2 dynamics due to inputs from major rivers (Amazon and Orinoco), substantial rainfall from the Intertropical Convergence Zone (ITCZ), and CO2-rich waters from equatorial upwelling. This study, spanning 1998 to 2018, utilized sea surface temperature (SST) and sea surface salinity (SSS) data from the PIRATA buoy at 8°N 38°W to reconstruct the surface marine carbonate system. Empirical models derived TA and DIC from SSS, with subsequent estimation of pH and fCO2 from TA, DIC, SSS, and SST data. Linear trend analysis showed statistically significant temporal trends: DIC and fCO2 increased and pH decreased, although DIC did not show any trend after data was de-seasoned. Rainfall analysis revealed distinct dry (July to December) and wet (January to June) seasons, aligning with lower and higher freshwater influence, respectively. TA, DIC, and pH correlated positively with SSS, exhibiting higher values during the dry season and lower values during the wet season. Conversely, fCO2 correlated positively with SST, showcasing higher values during the wet season and lower values during the dry season. This emphasizes the influential roles of SSS and SST variability in CO2 solubility within the region.

Description: In marine ecosystems, most physiological, ecological, or physical processes are size dependent. These include metabolic rates, the uptake of carbon and other nutrients, swimming and sinking velocities, and trophic interactions, which eventually determine the stocks of commercial species, as well as biogeochemical cycles and carbon sequestration. As such, broad-scale observations of plankton size distribution are important indicators of the general functioning and state of pelagic ecosystems under anthropogenic pressures. Here, we present the first global datasets of the Pelagic Size Structure database (PSSdb), generated from plankton imaging devices. This release includes the bulk particle normalized biovolume size spectrum (NBSS) and the bulk particle size distribution (PSD), along with their related parameters (slope, intercept, and R2) measured within the epipelagic layer (0–200 m) by three imaging sensors: the Imaging FlowCytobot (IFCB), the Underwater Vision Profiler (UVP), and benchtop scanners. Collectively, these instruments effectively image organisms and detrital material in the 7–10 000 µm size range. A total of 92 472 IFCB samples, 3068 UVP profiles, and 2411 scans passed our quality control and were standardized to produce consistent instrument-specific size spectra averaged to 1° × 1° latitude and longitude and by year and month. Our instrument-specific datasets span most major ocean basins, except for the IFCB datasets we have ingested, which were exclusively collected in northern latitudes, and cover decadal time periods (2013–2022 for IFCB, 2008–2021 for UVP, and 1996–2022 for scanners), allowing for a further assessment of the pelagic size spectrum in space and time. The datasets that constitute PSSdb's first release are available at https://doi.org/10.5281/zenodo.11050013 (Dugenne et al., 2024b). In addition, future updates to these data products can be accessed at https://doi.org/10.5281/zenodo.7998799.