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- 2015 (13) (entfernen)
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- Fachbereich 7 (13) (entfernen)
Global crop production increased substantially in recent decades due to agricultural intensification and expansion and today agricultural areas occupy about 38% of Earth’s terrestrial surface - the largest use of land on the planet. However, current high-intensity agricultural practices fostered in the context of the Green Revolution led to serious consequences for the global environment. Pesticides, in particular, are highly biologically active substances that can threaten the ecological integrity of aquatic and terrestrial ecosystems. Although the global pesticide use increases steadily, our field-data based knowledge regarding exposure of non-target ecosystems such as surface waters is very restricted. Available studies have by now been limited to spatially restricted geographical areas or had rather specific objectives rendering the extrapolation to larger spatial scales questionable.
Consequently, this thesis evaluated based on four scientific publications the exposure, effects, and regulatory implications of particularly toxic insecticides` concentrations detected in global agricultural surface waters. FOCUS exposure modelling was used to characterise the highly specific insecticide exposure patterns and to analyse the resulting implications for both monitoring and risk assessment (publication I). Based on more than 200,000 scientific database entries, 838 peer-reviewed studies finally included, and more than 2,500 sites in 73 countries, the risks of agricultural insecticides to global surface waters were analysed by means of a comprehensive meta-analysis (publication II). This meta-analysis evaluated whether insecticide field concentrations exceed legally accepted regulatory threshold levels (RTLs) derived from official EU and US pesticide registration documents and, amongst others, how risks depend on insecticide development over time and stringency of environmental regulation. In addition, an in-depth analysis of the current EU pesticide regulations provided insights into the level of protection and field relevance of highly elaborated environmental regulatory risk assessment schemes (publications III and IV).
The results of this thesis show that insecticide surface water exposure is characterized by infrequent and highly transient concentration peaks of high ecotoxicological relevance. We thus argue in publication I that sampling based on regular intervals is inadequate for the detection of insecticide surface water concentrations and that traditional risk assessment concepts based on all insecticide concentrations including non-detects lead to severely biased results and critical underestimations of risks. Based on these considerations, publication II demonstrates that out of 11,300 measured insecticide concentrations (MICs; i.e., those actually detected and quantified), 52.4% (5,915 cases; 68.5%) exceeded the RTL for either water (RTLSW) or sediments. This indicates a substantial risk for the biological integrity of global water resources as additional analyses on pesticide effects in the field clearly evidence that the regional aquatic biodiversity is reduced by approximately 30% at pesticide concentrations equalling the RTLs. In addition, publication II shows that there is a complete lack of scientific monitoring data for ~90% of global cropland and that both the actual insecticide contamination of surface waters and the resulting ecological risks are most likely even greater due to, for example, inadequate sampling methods employed in the studies and the common occurrence of pesticide mixtures. A linear model analysis identified that RTLSW exceedances depend on the catchment size, sampling regime, sampling date, insecticide substance class, and stringency of countries` environmental regulations, as well as on the interactions of these factors. Importantly, the risks are significantly higher for newer-generation insecticides (i.e., pyrethroids) and are high even in countries with stringent environmental regulations. Regarding the latter, an analysis of the EU pesticide regulations revealed critical deficiencies and the lack of protectiveness and field-relevance for current presumed highly elaborated FOCUS exposure assessment (publication IV) and overall risk assessment schemes (publication III). Based on these findings, essential risk assessment amendments are proposed.
In essence, this thesis analyses the agriculture–environment linkages for pesticides at the global scale and it thereby contributes to a new research frontier in global ecotoxicology. The overall findings substantiate that agricultural insecticides are potential key drivers for the global freshwater biodiversity crisis and that the current regulatory risk assessment approaches for highly toxic anthropogenic chemicals fail to protect the global environment. This thesis provides an integrated view on the environmental side effects of global high-intensity agriculture and alerts that beside worldwide improvements to current pesticide regulations and agricultural pesticide application practices, the fundamental reformation of conventional agricultural systems is urgently needed to meet the twin challenges of providing sufficient food for a growing human population without destroying the ecological integrity of global ecosystems essential to human existence.
Aquatic macrophytes can contribute to the retention of organic contaminants in streams, whereas knowledge on the dynamics and the interaction of the determining processes is very limited. The objective of the present study was thus to assess how aquatic macrophytes influence the distribution and the fate of organic contaminants in small vegetated streams. In a first study that was performed in vegetated stream mesocosms, the peak reductions of five compounds were significantly higher in four vegetated stream mesocosms compared to a stream mesocosm without vegetation. Compound specific sorption to macrophytes was determined, the mass retention in the vegetated streams, however, did not explain the relationship between the mitigation of contaminant peaks and macrophyte coverage. A subsequent mesocosm study revealed that the mitigation of peak concentrations in the stream mesocosms was governed by two fundamentally different processes: dispersion and sorption. Again, the reductions of the peak concentrations of three different compounds were in the same order of magnitude in a sparsely and a densely vegetated stream mesocosm, respectively, but higher compared to an unvegetated stream mesocosm. The mitigation of the peak reduction in the sparsely vegetated stream mesocosm was found to be fostered by longitudinal dispersion as a result of the spatial distribution of the macrophytes in the aqueous phase. The peak reduction attributable to longitudinal dispersion was, however, reduced in the densely vegetated stream mesocosm, which was compensated by compound-specific but time-limited and reversible sorption to macrophytes. The observations on the reversibility of sorption processes were subsequently confirmed by laboratory experiments. The experiments revealed that sorption to macrophytes lead to compound specific elimination from the aqueous phase during the presence of transient contaminant peaks in streams. After all, these sorption processes were found to be fully reversible, which results in the release of the primarily adsorbed compounds, once the concentrations in the aqueous phase starts to decrease. Nevertheless, the results of the present thesis demonstrate that the processes governing the mitigation of contaminant loads in streams are fundamentally different to those already described for non-flowing systems. In addition, the present thesis provides knowledge on how the interaction of macrophyte-induced processes in streams contributes to mitigate loads of organic contaminants and the related risk for aquatic environments.
Synthetische Nanopartikel sind neuartige Schadstoffe. Aufgrund ihrer häufigeren Anwendung wird sich ihre Konzentration in der Umwelt in Zukunft voraussichtlich stark erhöhen. Die Untersuchung des Schicksals von synthetischen Kolloiden in der Umwelt erweist sich als schwierig, bedingt durch deren mögliche komplexe Wechselwirkungen mit den Bestandteilen aquatischer Systeme. Eine zentrale Rolle spielt hierbei die Lösungschemie. Insbesondere die Wechselwirkungen mit gelösten organischen Stoffen (DOM) sind bisher wenig verstanden.
Das Ziel dieser Arbeit bestand darin, angepasste analytische Methoden zu entwickeln, um die Effekte von DOM auf das Schicksal synthetische Kolloide in der Umwelt zu untersuchen.rnEine Literaturrecherche über die Wechselwirkungen den DOM mit anorganischen Kolloiden hat ergeben, dass es einen Mangel an systematischen Charakterisierungen von Kolloiden und DOM in den meisten Studien gibt, obwohl diese wesentlich wäre. Des Weiteren wäre die Erforschung der Fraktionierung von DOM auf Kolloiden bedeutend sowie die Untersuchungen der Effekte von DOM auf die dynamische Struktur von Agglomeraten. Für die Charakterisierung von niedrigkonzentrierten Agglomeraten in Umweltmedien werden passende analytische Techniken benötigt. Solche Techniken müssen genau, spezifisch, artefaktfrei (minimale Probenvorbereitung) und matrixunabhängig bei niedrigen Konzentrationen sein. Keine der üblichen Methoden (Mikroskopie, Lichtstreuungsmethode, Trenntechnicken) erfüllt alle diese Voraussetzungen. Jedoch stellt die Hydrodynamische Chromatographie gekoppelt mit Massenspektrometrie mit induktiv gekoppeltem Plasma (HDC-ICP-MS) einen vielversprechenden Kompromiss dar. Mit dieser Methode kann die Größe von anorganischen Partikeln in komplexen Medien und in Konzentrationsbereichen unter ppb elementspezifisch gemessen werden. Allerdings wurden die Begrenzungen der Methode nicht systematisch untersucht.
Während dieser Doktorarbeit wurde das Potenzial dieser Methode weiter untersucht. Der einfache Trennmechanismus ermöglicht einen großen Spielraum für die Elutionsparameter und eine universelle Kalibrierung kann für Partikel mit unterschiedlicher Zusammensetzung und unterschiedlicher Oberflächenchemie angewendet werden. Eine schwache Auflösung der Partikelgröße sowie die Effekte der Partikelform auf den Retentionsfaktor stellen die wichtigsten Begrenzungen der Methode dar.rnDie Anwendung von HDC gekoppelt mit Einzelpartikel ICP-MS (HDC-SP-ICP-MS) bietet neue Möglichkeiten für die Partikelformerkennung und die Differenzierung zwischen primären Partikeln und Homoagglomeraten. Diese Kopplungstechnik ist deswegen hochattraktiv, um Effekte von DOM auf der Stabilität von Kolloiden zu untersuchen. Die Vielseitigkeit der HDC-ICP-MS konnte durch verschiedene erfolgreiche Anwendungen hervorgehoben werden. Insbesondere wurde sie genutzt, um die Stabilität von zitrat-stabilisierte Silberkolloiden in synthetischem Flusswasser unter Anwesenheit verschiedener Typen DOM zu untersuchen. Diese Partikel waren mehr als eine Stunde stabil unabhängig von pH und vom Typ der DOM. Dieses Ergebnis deckt sich mit den Ergebnissen einer parallel publizierten Studie über die Stabilität von Silberkolloiden in Rheinwasser. Die direkte Untersuchung von DOM-Adsorption auf Kolloiden war mit UV- und Fluoreszenzdetektoren nicht möglich. Vorversuche wiesen darauf hin, dass die fluoreszierenden Huminsaüremoleküle auf Silberkolloiden nicht adsorbieren. Lösungen für die verbleibenden Schwierigkeiten in der Analyse der Wechselwirkungen der DOM werden vorgeschlagen und die vielfältigen Entwicklungs- und Anwendungserspektiven von HDC-(SP)-ICP-MS in den Umweltwissenschaften werden im Detail diskutiert.