Person: Schulze, Jona
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Veröffentlichung UV-Filter in Sonnenschutzmitteln - Bewertung hormonähnlicher Eigenschaften und möglicher Gefahren für die Umwelt(2020) Arning, Jürgen; Germer, Sabine; Hassold, Enken; Kaßner, Franziska; Schalles, Simone; Schulze, Jona; Stock, FraukeUV-Filtersubstanzen in Sonnencremes und anderen Kosmetika sind unverzichtbar, um die Bevölkerung und Erwerbstätige vor den schädlichen Effekten durch ein Übermaß an UV-Strahlung bei Aktivitäten im Freien zu schützen. Die Kehrseite der Medaille ist, dass es in Bezug auf einige der weit verbreiteten UV-Filter eine zunehmende Besorgnis gibt, dass diese Stoffe als endokrine Disruptoren in der Umwelt wirken können. Dieser Artikel beschreibt daher, warum endokrine Stoffe in der mwelt problematisch sind und zeigt anhand aktueller Beispiele, wie diese Substanzen innerhalb der EU identifiziert und reguliert werden können. Abschließend werden für Verbraucherinnen und Verbraucher Tipps gegeben, wie ein Eintrag von UV-Filtern aus Sonnencreme und Kosmetika in die Umwelt durch einfache Maßnahmen verringert und so der Zielkonflikt zwischen bestmöglichem Gesundheits- und Umweltschutz entschärft werden kann. In: UMID : Umwelt und Mensch - Informationsdienst ; Umwelt & Gesundheit, Umweltmedizin, Verbraucherschutz / Boden- und Lufthygiene (Berlin) Institut für Wasser-. - (2020), Heft 2, Seite 17Veröffentlichung Diverging trends of plasticizers (phthalates and non-phthalates) in indoor and freshwater environments - why?(2022) Birmili, Wolfram; Koschorreck, Jan; Nagorka, Regine; Schulze, JonaBackground European chemicals management aims to protect human health and the environment from legacy and emerging contaminants. The plasticizer market changed in response to the restriction of low molecular weight (LMW) phthalate plasticizers such as Di (2-ethylhexyl) phthalate (DEHP) due to their hazardous properties. We investigated patterns and trends of 19 regulated and emerging plasticizers in house dust from German homes and in suspended particulate matter (SPM) from major German rivers. The samples were used from the mid-2000s and late 2010s from two governmental long-term monitoring programs in Germany. Results While the sum of the respective plasticizer levels hardly changed over the study period, we observed a significant decrease of LMW phthalates in both house dust (2003/06, 80% of the (Sigma)plasticizer concentration; 2014/17, 31%) and SPM (2005, 48%; 2017, 28%). This was accompanied by their substitution with high molecular weight (HMW) phthalates and non-phthalates. HMW phthalates increased from 19% of the (Sigma)plasticizer concentration to 46% between the mid-2000s and the late 2010s in house dust, and from 50% to 63% in SPM samples. Diisononyl phthalate (DINP) replaced DEHP as the dominant plasticizer in both compartments. A significant tenfold increase (p<0.05) was observed in SPM samples for Di (2-propylheptyl) phthalate (DPHP) (1-13%), compared to low levels in house dust (2014/17, 1%). Non-phthalates increased to 23% of the (Sigma)plasticizer concentration in house dust but only to 9% in SPM (mid-2000s: house dust,<1%; SPM, 1.5%). In recent house dust samples, Di (2-ethylhexyl) terephthalate (DEHT) had the third highest concentration of all plasticizers and contributed 18% to the total load, whereas Tris (2-ethylhexyl) trimellitate (TOTM) was one of the major non-phthalates in SPM samples. Conclusions Unlike in the indoor environment, the substitution of LMW phthalates in the aquatic environment was characterized by a significant shift towards plasticizers with potentially hazardous properties. DPHP and TOTM were identified by European chemical regulation as potentially endocrine disrupting compounds and persistent, bioaccumulative and toxic compounds. Our data document the need for integrated chemicals management to safeguard the transition to a non-toxic environment. © The Author(s) 2022Veröffentlichung Options for an environmental risk assessment of intentional and unintentional chemical mixtures under REACH(2021) Galert, Wiebke; Hassold, Enken; Schulze, JonaIt is acknowledged that a variety of chemicals enter the environment and may cause joint effects. Chemicals regulated under the European Chemicals Regulation REACH are often part of formulated mixtures and during their processing and use in various products they can be jointly released via sewage treatment plants or diffuse sources, and may combine in the environment. One can differentiate between intentional mixtures, and unintentional mixtures. In contrast to other substance-oriented legislations, REACH contains no explicit requirements for an assessment of combined effects, exposures and risks of several components. Still, it requires ensuring the safe use of substances on their own, in mixtures, and in articles. The available options to address intentional as well as unintentional mixtures are presented and discussed with respect to their feasibility under REACH, considering the responsibilities, communication tasks and information availability of the different actors (registrants, downstream-user and authorities). Specific mixture assessments via component-based approaches require a comprehensive knowledge on substances properties, uses, fate and behaviour, and the composition of the mixture under consideration. This information is often not available to the responsible actor. In principle, intentional mixtures of known composition can be assessed by the downstream-user. But approaches have to be improved to ensure a transparent communication and sound mixture assessment. In contrast, unintentional mixtures appear to be better addressable via generic approaches such as a mixture allocation factor during the chemical safety assessment, although questions on the magnitude, implementation and legal mandates remain. Authorities can conduct specific mixture risk assessments in well-defined and prioritized cases, followed by subsequent regulatory measures. In order to address intentional and unintentional mixtures within the current REACH framework, legal mandates together with guidance for the different actors are needed. Furthermore, further data on mixture compositions, uses and co-exposures need to be made accessible via shared databases. © The Author(s) 2021.Veröffentlichung PFAS-Substanzen sollen verboten werden, was zu Sorgen in der Galvanikbranche führt. Was macht diese Stoffe gefährlich?(2023) Schulze, Jona; Deutschland. Umweltbundesamt. Fachgebiet IV.2.3-ChemikalienVeröffentlichung Comprehensive target analysis and TOP assay of per- and polyfluoroalkyl substances (PFAS) in wild boar livers indicate contamination hot-spots in the environment(2023) Rupp, Jana; Guckert, Marc; Drost, Wiebke; Berger, Urs; Schulze, JonaThe suitability of wild boar liver as a bioindicator of per- and polyfluoroalkyl substances (PFAS) in the terrestrial environment was investigated. Samples from 50 animals in three different areas associated with (1) contaminated paper sludges distributed on arable land (PS), (2) industrial emissions of PFAS (IE) and (3) background contamination (BC) were analyzed for 66 PFAS, including legacy PFAS, novel substitutes and precursors of perfluoroalkyl acids (PFAAs). Additionally, the Total Oxidizable Precursor (TOP) assay was performed to determine the formation potential of PFAAs from precursors. In total, 31 PFAS were detected with site-specific contamination profiles. PFAS concentrations in livers from area PS and IE (567 and 944 (micro)g kg-1 wet weight, respectively) were multiple times higher than from area BC (120 (micro)g kg-1). The dominating PFAS were the legacy compounds perfluorooctane sulfonic acid (PFOS) in areas PS and BC (426 and 82 (micro)g kg-1, respectively) and perfluorooctanoic acid (PFOA) in area IE (650 (micro)g kg-1). In area IE, the compounds 4,8-dioxa-3H-perfluorononanoic acid (DONA) and hexafluoropropylene oxide dimer acid (HFPO-DA) - which are used as substitutes for PFOA - were determined at 15 and 0.29 (micro)g kg-1, respectively. The formation potential of PFAAs was highest in area PS, but generally lower than the contamination with PFAAs. The pattern of perfluoroalkyl carboxylic acids (PFCAs) in wild boar liver reflects the contamination of the local soil at the two hot-spot areas IE and PS. This first comparison of PFAS contamination between wild boars and soil suggests that wild boar livers are suitable bioindicators for PFAS contamination in the terrestrial environment. Moreover, in terrestrial samples from area IE, legacy PFAS were found to be retained for a longer period as compared to riverine samples (suspended particulate matter and chub filet). © 2023 The Authors