In the Earth, the dynamo action is strongly linked to core freezing. There is a solid inner core, the growth of which provides a buoyancy flux that drives the dynamo. The buoyancy in this case derives from a difference in composition between the solid inner core and the fluid outer core. In planetary bodies smaller than the Earth, however, this core differentiation process may differ - Fe may precipitate at the core-mantle boundary (CMB) rather than in the center and may fall as iron snow and initially remelt with greater depth. A chemical stable sedimentation zone develops that comprises with time the entire core - at that time a solid inner core starts to grow. The dynamics of this system is not well understood and also whether it can generate a magnetic field or not. The Jovian moon Ganymede, which shows a present-day magnetic dipole field, is a candidate for which such a scenario has been suggested. We plan to study this Fe-snow regime with both a numerical and experimental approach. In the numerical study, we use a 2D/3D thermo-chemical convection model that considers crystallization and sinking of iron crystals together with the dynamics of the liquid core phase (for the 3D case the influence of the rotation of the Fe snow process is further studied).The numerical calculations will be complemented by two series of experiments: (1) investigations in metal alloys by means of X-ray radioscopy, and (2) measurements in transparent analogues by optical techniques. The experiments will examine typical features of the iron snow regime. On the one hand they will serve as a tool to validate the numerical approach and on the other hand they will yield important insight into sub-processes of the iron snow regime, which cannot be accessed within the numerical approach due to their complexity.
Background Society aims for a pollutant-free environment, reflected in initiatives under the European Green Deal, which seek to reduce hazardous substances and promote safe, sustainable chemical use. Comprehensive exposure data are needed to identify sources, understand mixtures and eliminate sources of chemical pollution. High-resolution mass spectrometry non-target screening (HRMS NTS) is increasingly used in environmental regulatory context to chemically characterise the environment as completely as possible and retrospectively screen for known and emerging substances. Results This study provides use cases for monitoring and chemicals management with data from the German NTSPortal, a database and visualisation tool for HRMS NTS data from surface water and suspended particulate matter of major German rivers. Its internal spectral library enables substance identification comparable to standardised target analysis, supporting regulatory acceptance of HRMS NTS data for prioritisation and mixture assessment. To demonstrate its potential to research and regulation, we characterised the spatial and temporal distribution of riverine chemical mixtures and present selected use cases relevant to EU environmental, emission, and chemical legislation. Despite pronounced spatial variability, mixture composition based on presence–absence data remained stable over time, with 855 of 1721 substances detected at least once and 247 occurring ubiquitously. Declining trends for regulated substances such as carbendazim and climbazole illustrate the effectiveness of regulatory measures. Overall, the results showed that NTS data repositories can help overcome fragmented exposure information and enable more consistent use of monitoring data across policy areas, including evaluation of the revised Urban Waste Water Treatment Directive and One Health concepts. Conclusions Data from the German NTSPortal enabled a multi-matrix and temporal characterisation of riverine chemical mixtures, revealing both stable mixture compositions over time and persistent, catchment-specific substances. These data facilitated high-resolution mixture assessments across space and time, alongside trend analyses that meet regulatory needs in environmental monitoring and chemical risk assessment. Further temporal, spatial, chemical and matrix-spanning expansion of HRMS NTS repositories will enhance their value for environmental monitoring programmes. Strengthening interoperability, implementing FAIR data principles, and developing advanced tools for prioritisation, quantification and toxicity prediction, including AI-based approaches, will be crucial to fully realise the regulatory potential of NTS portals in the future. © The Author(s) 2026.
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.
Globally, agriculture covers 40% of the earth’s surface and food systems are responsible for one-third of humanity’s contribution to global climate change. Yet, smallholder and subsistence farmers are among the most vulnerable to climate change, with extreme weather events and related food price volatility affecting livelihoods, biodiversity, and food security at multiple scales. This project builds on transdisciplinary research on agroecological transitions in vulnerable farming communities in Canada, Germany, India and Brazil. We will examine the influence of agroecological networks (farming organizations, institutional actors, and consumer groups) in promoting the perennialization of agriculture to support climate adaptation (improving resilience in livelihoods and food security) and mitigation (increasing carbon sequestration). Perennialization of agriculture integrates annual and perennial crops and trees into the same farming system. Compared to annual cropping systems which currently dominate global agriculture and markets, perennial crops show promise for climate adaptation and mitigation because of their contributions to carbon sequestration in tree biomass and soil organic carbon, and their buffering effects against soil degradation, drought, and other forms of extreme weather and climate variability. From a social wellbeing perspective, agroforestry and other diversified perennial systems offer opportunities to adapt to climate change and escape poverty traps, including higher and more stable farm incomes, balanced agricultural labour across growing seasons, improved working conditions compared to more input-intensive forms of agriculture and improved nutrition and health. Using a participatory action research approach, this project will use a novel methodology to test the relationships between personal, political, and practical leverage points driving the adoption of agroforestry and other practices supporting agricultural perennialization. We will sample farms and organizations in each case study across a diversification gradient from low-diversity farming systems to perennial and agroforestry-based management systems. We will then use qualitative and quantitative methods to assess climate resilience outcomes and estimate the potential of scaling adoption of perennial and agroforestry practices. A cross-case synthesis will take local institutional, environmental, and relational contexts into account to inform decision-making.
In recent years science has taken an increased interest in mineralization processes in tropical soils in particular under minimal tillage operations. Plant litter quality and management strongly affect mineralization-nitrification processes in soil and hence the fate of nitrogen in ecosystems and the environment. Plant secondary metabolites like lignin and polyphenols are poorly degradable and interact with proteins (protein binding capacity) and hence protect them from microbial attack. Nitrification, a microbiological process, directly and indirectly influences the efficiency of recovery of N in the vegetation as well as the loss of N (through denitrification and leaching) causing environmental pollution to water bodies and contributes to global warming (e.g. the greenhouse gas N2O is emitted as a by-product of nitrification and denitrification). Nitrifiers comprise a relatively narrow species diversity (at least as known to date) and are generally thought to be sensitive to low soil pH and stress. Despite these properties nitrification occurs in acid tropical soils with high levels of aluminium and manganese. Thus the main objective of the project will be the identification of micro-organisms and mechanisms responsible for mineralization-nitrification processes in acid tropical soils and the influence of long-term litter input of different chemical qualities and minimal tillage options. The project will include the use of stable isotopes (15N, 13C), mass spectrometry, gas chromatography (CO2, N2O), biochemical methods (PLFA) and molecular biology (16s rRNA., PCR, DGGE)
In hydrology, the relationship between water storage and flow is still fundamental in characterizing and modeling hydrological systems. However, this simplification neglects important aspects of the variability of the hydrological system, such as stable or instable states, tipping points, connectivity, etc. and influences the predictability of hydrological systems, both for extreme events as well as long-term changes. We still lack appropriate data to develop theory linking internal pattern dynamics and integral responses and therefore to identify functionally similar hydrological areas and link this to structural features. We plan to investigate the similarities and differences of the dynamic patterns of state variables and the integral response in replicas of distinct landscape units. A strategic and systematic monitoring network is planned in this project, which contributes the essential dynamic datasets to the research group to characterize EFUs and DFUs and thus significantly improving the usual approach of subdividing the landscape into static entities such as the traditional HRUs. The planned monitoring network is unique and highly innovative in its linkage of surface and subsurface observations and its spatial and temporal resolution and the centerpiece of CAOS.
This dataset contains measurements from LP20190603, collected aboard the R/V Ludwig Prandtl in June 2019 in the Elbe Estuary. In a transect cruise, geobiochemical parameters were measured starting in the North Sea (53.98°N 8.36°E) to the port of Oortkaten in the upstream Elbe Estuary (53.46°N 10.06°E). Sampling was conducted upstream against the outgoing tide to prevent tidal effects on the measurements. Water samples were taken approximately every 20 min. The discrete water samples were used to measure dissolved inorganic nutrient, nitrate stable isotope composition, suspended particulate matter (SPM) concentration, particulate carbon and nitrogen content of SPM and nitrogen stable isotope composition of SPM. An onboard membrane pump provided the on-line in situ FerryBox system. It continuously measured oxygen, salinity, and temperature during the cruise. A N2O analyzer coupled (Model 914-0022, Los Gatos Res. Inc., San Jose, CA, USA) with a seawater/gas equilibrator using off-axis cavity output spectroscopy continuously detected dry mole fraction of dissolved nitrous oxide along the estuary. Aim of the cruise was to study the interplay between eutrophication, in-stream nutrient regeneration and N2O emissions in a temperate Estuary.
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.
Cloud samples for the isotopic analysis were collected in the framework of the Hill Cap Cloud Thuringia 2010 (HCCT-2010) campaign on Schmücke (50° 39'N/ 10° 46'E, 937 m a.s.l.; Germany) in September and October 2010 with a three-stage Caltech Active Strand Cloudwater Collector (CASCC) during 13 different cloud events with a temporal resolution of 1 to 3 hours. In a first step, we ensured that no additional fractionation occurred during sampling with the CASCC. The d values of the three sizes classes of the CASCC (4 µm to 16 µm, 16 µm to 22 µm and >22 µm) did not differ significantly, revealing that the cloud droplets of different sizes quickly equilibrate their delta value with the one of the surrounding vapor. delta values in the cloud droplets varied from -77 per mil to -15 per mil in d2H and from -12.1 per mil to -3.9 per mil in d18O and were fitted by d2H =7.8*d18O +13*10**-3. delta values decreased with temperature as well as towards the end of the campaign, representing a seasonal trend which is known from d values in precipitation. The deuterium excess of the cloud samples was generally higher than the Local Meteoric Water Line of the closest GNIP (Global Network of Isotopes in Precipitation) station. Rain decreases its deuterium excess during falling through an unsaturated air column, while the cloud droplets conserve the deuterium excess of the initial evaporation and thus have been found to be a good indicator for the airmass source region: higher deuterium excess was measured for polar air masses and lower deuterium excess for Mediterranean air masses. Changes in d values during one cloud event were up to 3.6 per mil (d2H) and 0.23 per mil (d18O), except for frontal passages, which were associated with increases of ~6 per mil per hour (d2H) and ~0.6 per mil per hour (d18O). Using a box model, we showed that the influence of condensation only was able to explain the variation in the isotope signal of two cloud passages. Consequently, we deduced that the water vapor "feeding" the cloud advected the measured changes. A trajectory analysis and moisture source diagnostic revealed that it is very likely that the variations were either related to rain out along the trajectories or to meteorological changes in the moisture source region. This was the first study using stable water isotopologues in cloud water manifesting their potential in the context of atmospheric water vapor circulation.
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.
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