Anreicherung und Verteilung von Schwermetallen und anderen Elementen in Oberflächensedimenten der Berliner Gewässer und ihres Umlands Enrichment and Distribution of Heavy Metals and Other Elements in Surface Sediments of Berlin Waters (Germany) and their Surroundings

For a wide variety of substances aquatic systems are the medium of origin, or sinks in a longer or shorter lasting stay or even in geological periods. For surface sediments of Berlin waters and their surroundings this paper describes the enrichment and distribution of heavy metals (SM), which have a high priority under international aspects and a marked capability to geoaccumulation. From the 25 metals investigated Hg, Pb, Cu, Cd and Zn are of anthropogenic origin, all others are of geochemical provenience and correspond to background values. Some metals (Hg, Cd, Ni, Co, Cu, Cr and Pb) have specific concentration profiles with increasing depth of water and sediment. The study of correlation of SM in sediments demonstrates generally a strong relation to macroelements and between some metals themselves.     

Formation of Humic-like Substances in Mixed and Pure Cultures of Aquatic Microorganisms

A natural decay of plant and animal biomass in aquatic environments results in the release of different simple structured organic substances into water. In our laboratory experiments we investigated whether some of them, e.g., starch or peptone, and also a complex yeast biomass can be transformed into humic-like substances by natural assemblages and some pure cultures of aquatic microorganisms. After a 6 months incubation most of the cultural media enriched with those natural organic substrates turned dark in color and humic-like substances (HS) could be isolated. However, the original substrate organic carbon was mainly mineralized in microbial cultures, and only about 3 % C was converted into HS. Total yields of HS differed in dependence of the individual substrate used (peptone > yeast > starch), the origin of inoculum (river > lake > groundwater), and the incubation temperature (20°C > 10°C). According to their elemental composition, and their spectroscopical and electrophoretic characteristics the microbially formed HS resembled natural aquatic humic matter, but were higher in aliphatic constituents (carbohydrates, peptides) and lower in aromatic structures. HS-like substances were also obtained from pure cultures of a bacterium Bacillus sphaericus and a fungus Cladosporium cladosporioides. The ¹³C and ¹⁵N isotopic contents of the microbially produced HS differed in dependence on the microbial inoculum and the type of organic substrates used, but in general they indicated anabolic processes to be mainly responsible for the humification of the simple organic substrates used in our experiments.     

Verteilung ausgewählter toxischer Spurenelemente im Sediment des Breitlingsees bei Brandenburg

Distribution of Selected Toxic Trace Elements in the Sediment of Lake Breitling near Brandenburg. Considerable enrichments of several heavy metals in relation to the local geological background were found in the surface sediments of Lake Breitling (Havel lake system) (Zn: 50-fold, Cd: 25-fold, Cu: 14-fold, Pb: 13-fold), whereas Be, Co and V are remarkably unchanged if the increased clay mineral content in the more recent sediments is considered. – The heavy metal distribution patterns indicate a high percentage of atmospheric input of these elements, and according to geochemical profiles heavy metal deposition has been constant on a high level for years. – Especially the most enriched Zn which was found to some extent NH₄Ac-exchangeable deserves ecotoxic attention.     

TOC-Bestimmung in Schlämmen,Sedimenten und Schwebstoffen — Beschreibung des Verfahrens und begleitender Qualitätssicherungsmaßnahmen Determination of TOC in Sludge,Sediment and Suspended Solids — Description of the Analytical Procedure and Accompanying Quality Control Procedures

The total organic carbon (TOC) is calculated by subtracting the inorganic carbon (IC) from the total carbon (TC). For TC determination, the carbon in a sample is completely converted to CO₂ by decomposition/combustion in an oxygen stream. To determine IC, inorganic carbon (carbonate) is liberated by adding acid and by heating in an oxygen stream. In both cases, CO₂ is quantified by infrared spectrometry. To gain reliable and reproducable results for sludge, sediment and suspended solids, at least the following conditions have to be met: particle size has to be smaller than 200 μm; weightout has to be selected in such a way, that the signal area is not below and the signal maximum is not above specific instrument dependent parameters; combustion/decomposition has to be complete (TC: ≥ 1300 °C, no soot) and rules for analytical quality assurance must be followed. The TC quantification of calcium carbonate is used for system calibration. Daily working procedures include calibration checks by mean control charts for TC determination of calcium carbonate and IC determination of sodium carbonate as well as for control sediment TC and IC quantifications.     

Historische Entwicklung einer Sedimentbelastung: Gedächtnis einer Industrieregion Historical Trends of Sediment Loads: Memory of an Industrial Region

The chronologies are shown of sediment load on the banks of a river of the Ruhr district (Lippe) with radionuclides of radium, lead and cesium and preliminary chemical measurements for lead, zinc, arsenic, mercury, cadmium, barium, PAHs, PCDDs, PCDFs, PCBs, TOC, AOX and EOX. A new method of dating is developed and proved, which is especially suitable for rivers with radioactivity from coal mines. The method improves the well-known excess-²¹⁰Pb-dating for the use with rivers in industrial regions and allows the preparation of load histories (chronologies). Conclusions are made on the historical trend of emissions in the region from the trend of the sediment load of known age and regular sedimentation without perturbation.     

UV-Derivativ-Spektren zur Vorabschätzung des Gehaltes von polycyclischen aromatischen Kohlenwasserstoffen in Schwebstoffen und Sedimenten der Gewässer Derivative UV Spectra for Estimating the Contents of Polycyclic Aromatic Hydrocarbons in Suspended Solids and Sediments of Waters

By means of UV spectra of cyclohexane extracts from aquatic sediments it is possible to distinguish: “normal” mineral oil aromatics (e. g. of the middle distillation fraction), used oils, and highboiling raffinates, tar oils, and — as representative of aromatics listed in the German drinking water ordinance — fluoranthene. Starting with less selective extractants and the basic UV spectra, it is shown that spectra of higher orders frequently allow a quantitative determination of fluoranthene. If it is justified to assume a constant conversion factor, the result of the measurement can be used to calculate the contents of the whole group of aromatics listed in the German drinking water ordinance. A comparison with other methods (HPLC etc.) and with results from other laboratories showed good agreement. Finally, the diagnostic capacity (fingerprint) of derived spectra is pointed out.     

Degradation and Transformation of Aquatic Humic Substances by Laccase-producing Fungi Cladosporium cladosporioides and Polyporus versicolor

A phenoloxidase-producing fungus – Cladosporium cladosporioides – was isolated from water of a bog lake. At high concentrations of carbon (333 mM) and nitrogen (12 mM), the fungus demonstrated the formation of a laccase and a high ligninolytic activity. After addition of riverine or groundwater humic substances into culture media (ca. 1 mg mL^–1), the fungus showed the ability of degrading (utilizing) of about 60% of these substances. However, the exact quantification of the degree of degradation was difficult because of adsorption of humic matter on fungal mycelium. Reisolated humic substances were lower in aromatic and higher in aliphatic structures. A crude enzyme from the C. cladosporioides culture showed only low activity in decolorizing humic substances, whereas decolorization up to 50% was observed when using a laccase preparation from Polyporus versicolor, and especially in the presence of a redox mediator.     

Bestimmung von Umweltqualitätsnormen für potenziell gewässerrelevante Stoffe

With the Water Framework Directive (WFD) the European Commission (EC) is requested to define environmental quality standards for pollutants to protect aquatic life in surface waters. Quality standards have to be derived by a scientific risk assessment and should not be exceeded. The recommended quality standards are mainly based on long term toxicological tests with algae, crustaceans and fish. The lowest effect concentration is divided by an assessment factor between 10 and 1000, which considers the data quality and quantity. In this work funded by the German Länder Working Party on Water (Länderarbeitsgemeinschaft Wasser – LAWA) environmental quality standards for 40 considered relevant substances were derived for aquatic ecosystems. The data sheets cover the identification of the compounds, their behaviour in the environment (physical‐chemical properties, biotic and abiotic degradation, sorption, bioaccumulation), information about mode of action, uses, analytical determination and available quality criteria. Ecotoxicological effect concentrations for bacteria, algae, protozoa, aquatic plants, crustaceans, fish, amphibians, insects and molluscs are listed. For 17 of the 40 hazardous substances investigated, quality objectives above 1 μg/L were derived. For 12 substances the values were between 0.1 μg/L and 1 μg/L and for 5 substances lower than 0.1 μg/L. Incomplete ecotoxicological data sets of the remaining compounds do not allow the derivation of quality standards. Especially for drugs further ecotoxicological test results are needed.