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Member States' use of revenues from the auctioning of EU ETS allowances, 2020-2024

This metadata overs the dataset containing information on how EU Member States spend the revenues from auctioning EU ETS emission allowances in one calendar year. More information on the EU Emissions Trading System (EU ETS) can be found here. The revenues from the auctioning of these allowances represent an increasing income source for Member States. This data is being collected under Article 19 of the Governance Regulation. The Regulation’s aim is to help the EU reach its 2030 climate and energy targets by setting common rules for planning, reporting and monitoring. The Regulation also ensures that EU planning and reporting are synchronised with the ambition cycles under the Paris Agreement. Reporting is mandatory for EU Member States. Some information is only mandatory to report if the data is available.

Total suspended matter, particulate organic matter and particulate inorganic matter from discrete water samples during RV MARIA S MERIAN cruise MSM129/1

This dataset was collected during the cruise MSM129/1 with RV MARIA S. MERIAN from Warnemünde, Germany to St. John's, Canada. It contains suspended particulate matter, particulate organic matter and particulate inorganic matter measurements [mg/l] from water samples collected from the seawater supply (Reinseewassersystem, RSWS) to calibrate the turbidity data of the RSWS system. The outflow of a PocketFerrybox that was connected to the seawater supply in the hangar was used for sampling. It takes a substantial amount of time for the water to reach the hanger from the intake point. The time delay between the sensor readings of the RSWS and the PocketFerrybox was determined and the timestamps of the water sampling were adjusted accordingly. Given latitute and longitude refer to this corrected timestamp. The original time of water sampling in the hangar is given as an additional column with the comment time of sampling. To obtain suspended particulate matter concentrations, water samples were filtered onboard through 0.7 μm pore size, glass fiber filters (Whatmann GF/F, 47 mm) under low vacuum. Filters were frozen immediately at -80 °C until gravimetric analysis in the laboratory at ICBM, Wilhelmshaven according to IOCCG recommendations.

Use cases from the German NTSPortal on the systematic use of high-resolution mass spectrometry non-target screening data in environmental monitoring and chemicals management

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.

REACH Mindestanforderungen PBT

Konkretes Management von Substanzen von hoher Besorgnis im Rahmen von REACH; Exemplarische Beschreibung an Fallbeispielen.

Forschergruppe (FOR) 5094: Dynamik des tiefen Untergrundes von Hochenergiestränden, Teilprojekt Organisches Material: Abiotische Umwandlungen und mikrobielle Interaktionen

Durch DynaDeep wird ein Verständnis der Funktionsweise und Relevanz des Land-Meer Übergangs im Untergrund von Hochenergiestränden gewonnen werden. Wir nehmen an, dass dieser einen hoch dynamischen Bioreaktor und einzigartiges mikrobiologisches Habitat darstellt und Netto-Stoffflüsse in Richtung Meer stark beeinflusst. Um dieses Ziel zu erreichen werden sechs Teilprojekte gemeinsam Felduntersuchungen und experimentelle Arbeiten durchführen und diese mit mathematischen Modellen integrativ kombinieren. Teilprojekt P3 wird die Quellen, die Zusammensetzung und die Umwandlungen organischen Materials als Hauptfaktoren biogeochemischer Prozesse im tiefen subterranen Ästuar untersuchen. Wir verfolgen die Hypothese, dass der transiente Charakter des tiefen Untergrundes entscheidend für den Umsatz und die molekulare Umwandlung organischen Materials durch wechselwirkende abiotische und biotische Prozesse ist. Eine Kombination von gezielten Laborexperimenten und Feldarbeiten wird angewandt zur Identifizierung und Charakterisierung von (1) potentiellen Quellen des organischen Materials im tiefen subterranen Ästuar, (2) abiotischen Veränderungen der Menge und Zusammensetzung des gelösten organischen Materials (DOM) an zeitlich und räumlich variablen Redox-Grenzflächen, und (3) Abbau und Umwandlung von DOM durch mikrobielle Gemeinschaften. Dabei wird die detaillierte molekulare Information genutzt, um Zusammenhänge zwischen der DOM-Zusammensetzung und der Zusammensetzung und Aktivität der mikrobiellen Gemeinschaften zu entschlüsseln. Die Charakterisierung des organischen Materials erfolgt durch modernste molekulare Ansätze wie ultrahochauflösende Fourier-Transformations-Ionenzyklotronresonanz-Massenspektrometrie (FT-ICR-MS) und Ultra-Leistungs-Flüssigkeitschromatographie, ergänzt durch Analysen von stabilen und Radiokohlenstoff-Isotopen. Molekulare Marker werden als Diagnosewerkzeuge für spezifische biogeochemische Zustände des tiefen subterranen Ästuars und der daraus resultierenden mikrobiellen Nischen etabliert. Die Ergebnisse von P3 werden das gekoppelte hydrogeologische Transport-Reaktionsmodell (P6) mit Reaktivitätstermen bestücken und Informationen über Quellen und Alter von DOM (P1) liefern. Die in P3 gewonnenen molekularen Daten werden im Zusammenhang mit den Daten zur mikrobiellen Gemeinschaft (P5) und zur Verteilung der relevanten Spurenelemente (P4) interpretiert und tragen zu einem mechanistischen Verständnis der mikrobiellen Atmung bei (P2).

Potentiell TFA-emittierende Industriebetriebe (Datensatz)

Für die sehr persistente und sehr mobile Verbindung Trifluoracetat (TFA) werden die potentiell TFA-emittierenden Industriebetriebe dargestellt, die im Rahmen des Gutachtens „Trifluoracetat (TFA): Grundlagen für eine effektive Minimierung schaffen - Räumliche Analyse der Eintragspfade in den Wasserkreislauf“ (Laufzeit: August 2021-November 2022) ermittelt wurden. Wichtiger Hinweis: Informationen zu Industriebetrieben in Deutschland, die TFA direkt in die aquatische Umwelt emittieren, lagen nicht vor. Daher können keine Aussagen zur Relevanz des Eintragspfads Industrie für die TFA-Fracht in Fließgewässern in Deutschland und zum Standort TFA-emittierender Betriebe getroffen werden. Ob und in welchem Umfang die aufgezeigten Betriebe tatsächlich TFA in die aquatische Umwelt emittieren, kann an dieser Stelle nicht beantwortet werden. Hier wird daher lediglich die Lage der Betriebe in Deutschland dargestellt, welche laut der Angaben im E-PRTR-Register Betriebe sind, die Fluor oder Fluor-haltige Verbindungen emittieren oder nach Artikel 10 der REACH-Verordnung registriert sind. Die Daten lassen jedoch keine Rückschlüsse auf die tatsächlich im Betrieb produzierten und/oder verarbeiteten fluorierten Chemikalien zu. Genauere Hinweise befinden sich im Abschnitt Herkunft des Datenkatalogs.

Strategic Partnership on Testing of REACH

Chlorophyll a and phaeophytin a measurements from discrete water samples during RV MARIA S. MERIAN cruise MSM129/1

This dataset was collected during the cruise MSM129/1 with RV MARIA S. MERIAN from Warnemünde, Germany to St. John's, Canada. It contains chlorophyll-a measurements [µg/l] from water samples collected from the seawater supply (Reinseewassersystem, RSWS) as well as from three CTD casts to calibrate the fluorometers of the RSWS system and the CTD, respectively. The outflow of a PocketFerrybox that was connected to the seawater supply in the hangar was used for sampling. It takes a substantial amount of time for the water to reach the hanger from the intake point. The time delay between the sensor readings of the RSWS and the PocketFerrybox was determined and the timestamps of the water sampling were adjusted accordingly. Given latitute and longitude refer to this corrected timestamp. The original time of water sampling in the hangar is given as an additional column with the comment time of sampling. To obtain chl-a concentrations, water samples were filtered onboard through 0.7 μm pore size, glass fiber filters (Whatmann GF/F) under low vacuum. Filters were frozen immediately at -80 °C until extraction in laboratory by 90% acetone method. Concentrations were calculated from fluorescence measured with a pre-calibrated Turner Design TD 7200-02 laboratory fluorometer (EPA445.0, Turner Manual).

Distribution and concentration of nutrients, carbon compounds and methane in water samples in the southern German Bight during RV HEINCKE cruise HE673/2, MOSES Sternfahrt 15 in November 2025

Previous Sternfahrten were mainly conducted in spring and summer. To cover the seasonal aspects more thoroughly, including a winter situation, this cruise was conducted in late autumn (20 -22 November 2025 ). We used the RV Heincke (cruise HE673/2) instead of the RV Uthörn. The Heincke's draught is greater, so we could not reach all of our previous stations. Surface and bottom water samples were taken with a rosette.

Total alkalinity and pH in the alkalization mesocosms of a chronic Ostrea edulis alkalinity-enhancement exposure experiment

This dataset contains repeated measurements of seawater pH and total alkalinity recorded in the alkalinization mesocosms, a set of tanks without oysters that received the same alkalinity treatments as the exposure mesocosms reported in a companion dataset. Total alkalinity was raised in three alkalization cycles to reach target increases of +250 or +500 µmol/kg over unamended seawater, using either dissolved alkalinity addition (NaOH and CaCl2) or olivine-based coastal enhanced silicate weathering. The three cycles ran 17 April to 7 May 2024, 8 May to 27 May 2024 and 30 May to 19 June 2024. Measurements were taken predominantly in triplicate per treatment and sampling day. Seawater pH was measured with a pH electrode and total alkalinity by open-cell potentiometric titration, both on a Metrohm 855 Robotic Titrosampler.

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