The suitability of caffeine as a chemical marker for surface water pollution by domestic wastewaters was assessed in this study. Caffeine concentrations in influents and effluents of Swiss wastewater treatment plants (WWTPs, 7-73 and 0.03-9.5 microg/L, respectively) indicated an efficient elimination of 81-99.9%. Corresponding loads in untreated wastewater showed small variations when normalized forthe population discharging to the WWTPs (15.8 +/- 3.8 mg person(-1) d(-1)), reflecting a rather constant consumption. WWTP effluent loads were considerably lower (0.06 +/- 0.03 mg person(-1) d(-1)), apart from installations with low sludge age (< or = 5 d, loads up to 4.4 mg person(-1) d(-1)). Despite the efficient removal in most WWTPs, caffeine was ubiquitously found in Swiss lakes and rivers (6-250 ng/ L), except for remote mountain lakes (<2 ng/L; analytical procedure for wastewater and natural waters: SPE, GC-MS-SIM or GC-MS-MS-MRM, internal standard 13C3-labeled caffeine). Caffeine concentrations in lakes correlated with the anthropogenic burden by domestic wastewaters, demonstrating the suitability of caffeine as a marker. A mass balance for Greifensee revealed that approximately 1-4% of the wastewaters had been discharged without treatment, presumably on rainy days when the capacity of WWTPs had been exceeded. For Zürichsee, it could be shown that the monthly inputs of caffeine correlated with precipitation data. The depth- and seasonal-dependent concentrations in this lake were adequately rationalized by a numerical model considering flushing, biodegradation, and indirect photodegradation via HO. radicals as elimination processes and caffeine inputs as fitting variables.

Organic UV filters are used in personal care products such as sunscreen products, and in cosmetics, beauty creams, skin lotions, lipsticks, hair sprays, hair dyes, shampoos, and so forth. The compounds enter the aquatic environmentfrom showering, wash-off, washing (laundering), and so forth via wastewater treatment plants (WWTPs) ("indirect inputs") and from recreational activities such as swimming and bathing in lakes and rivers ("direct inputs"). In this study, we investigated the occurrence of four important organic UV filter compounds (benzophenone-3, BP-3; 4-methylbenzylidene camphor, 4-MBC; ethylhexyl methoxy cinnamate, EHMC; octocrylene, OC) in wastewater, and in water and fish from various Swiss lakes, using gas chromatographic/mass spectrometric analyses. All four UV filters were present in untreated wastewater (WWTP influent) with a maximum concentration of 19 microg L(-1) for EHMC. The data indicate a seasonal variation with influent loads higher in the warmer season (June 2002) than in the colder one (April 2002). The influent loads were in the order EHMC > 4-MBC approximately BP-3 > OC. The concentrations in treated wastewater (WWTP effluent) were considerably lower, indicating substantial elimination in the plants. 4-MBC was usually the most prevalent compound (maximum concentration, 2.7 microg L(-1)), followed by BP-3, EHMC, and OC. UV filters were also detected in Swiss midland lakes and a river (Limmat) receiving inputs from WWTPs and recreational activities. However, all concentrations were low (<2-35 ng L(-1)); no UV filters (<2 ng L(-1)) were detected in a remote mountain lake. Data from passive sampling using semipermeable membrane devices (SPMDs) supported the presence of these UV filters in the lakes and the river and suggested some potential for accumulation of these compounds in biota. SPMD-derived water concentrations increased in the order Greifensee < Zürichsee < Hüttnersee. This order is reversed from that observed for methyl triclosan, used as a chemical marker for WWTP-derived lipophilic contaminants in the lakes. This indicated inputs of UV filters from sources other than WWTPs to the lakes during summer,for example,inputs from recreational activities. Fish (white fish, Coregonus sp.; roach, Rutilus rutilus; perch, Perca fluviatilis) from these lakes contained low but detectable concentrations of UV filters, in particular, 4-MBC (up to 166 ng g(-1) on a lipid basis). 4-MBC concentrations relative to methyl triclosan were lower in fish than in SPMDs exposed in the same lakes, suggesting that 4-MBC is less bioaccumulated than expected or metabolized in fish. The lipid-based bioconcentration factor (BCF(L)) estimated from the fish (roach) data and SPMD-derived water concentrations was about 1-2.3 x 10(4) and thus approximately 1 order of magnitude lower than expected from its Kow value.

Pharmaceutical compounds can reach detectable concentrations in rivers and lakes if production and use are sufficiently large and the compounds show some mobility and persistence in the aquatic environment. In this study, we report on the occurrence and on the enantiomer composition of the chiral pharmaceutical drug ibuprofen (IB) in surface waters and in samples from wastewater treatment plants (WWTPs). Enantioselective gas chromatography and detection by mass spectrometry/mass spectrometry was used for analysis. IB was present in influents of WWTPs at concentrations of up to 3 µg/L with a high enantiomeric excess of the pharmacologically active S enantiomer (S . R), as from human urinary excretion. The principal human urinary metabolites of IB, hydroxy-IB and carboxy-IB, were observed in WWTP influents at even higher concentrations. In contrast to other pharmaceutical compounds such as clofibric acid and diclofenac, IB and its metabolites are then efficiently degraded (>95%) during treatment in WWTPs. Laboratory incubation experiments confirmed this rapid degradation. In rivers and lakes, IB was detected at concentrations of up to 8 ng/L, generally with some excess of the S enantiomer; the IB metabolites were not detected (<1 ng/L). Incubation of lake water fortified with (rac)-IB indicated a faster dissipation of the S enantiomer, thus resulting eventually in residues with a reversed (R > S) enantiomer composition as compared to that from human metabolism. Inefficient WWTPs and direct discharges of untreated wastewater from storm events, however, can still be a source for increased levels of IB in surface water.

Artificial low-calorie sweeteners are consumed in considerable quantities with food and beverages. After ingestion, some sweeteners pass through the human metabolism largely unaffected, are quantitatively excreted via urine and feces, and thus reach the environment associated with domestic wastewater. Here, we document the widespread occurrence of four sweeteners in the aquatic environment and show that one of these compounds, acesulfame, meets all of the criteria of an ideal marker for the detection of domestic wastewater in natural waters, particularly groundwater. Acesulfame was consistently detected in untreated and treated wastewater (12-46 microg/L), in most surface waters, in 65% of the investigated groundwater samples, and even in several tap water samples (up to 2.6 microg/L) from Switzerland. The sweetener was not eliminated in wastewater treatment plants (WWTPs) and was quite persistent in surface waters, where concentrations increased with population in the catchment area and decreased with water throughflow. The highest concentrations in groundwater, up to 4.7 microg/L, were observed in areas with significant infiltration of river water, where the infiltrating water received considerable discharges from WWTPs. Given the currently achieved detection limit of approximately 0.01 microg/L, it is possible to trace the presence of > or = 0.05% wastewater in groundwater.

The bactericide triclosan and methyl triclosan, an environmental transformation product thereof, were detected in lakes and in a river in Switzerland at concentrations of up to 74 and 2 ng L(-1), respectively. Both compounds were emitted via wastewater treatment plants (WWTPs), with methyl triclosan probably being formed by biological methylation. A regional mass balance for a lake (Greifensee) indicated significant removal of triclosan by processes other than flushing. Laboratory experiments showed that triclosan in the dissociated form was rapidly decomposed in lake water when exposed to sunlight (half-life less than 1 h in August at 47 degrees latitude). Methyl triclosan and nondissociated triclosan, however, were relatively stable toward photodegradation. Modeling these experimental data for the situation of lake Greifensee indicated that photodegradation can account for the elimination of triclosan from the lake and suggested a seasonal dependence of the concentrations (lower in summer, higher in winter), consistent with observed concentrations. Although emissions of methyl triclosan from WWTPs were only approximately 2% relative to those of triclosan, its predicted concentration relative to triclosan in the epilimnion of the lake increases to 30% in summer. Passive sampling with semipermeable membrane devices (SPMDs) indicated the presence of methyl triclosan in lakes with inputs from anthropogenic sources but not in a remote mountain lake. Surprisingly, no parent triclosan was observed in the SPMDs from these lakes. Methyl triclosan appears to be preferentially accumulated in SPMDs under the conditions in these lakes, leading to concentrations comparable to those of persistent chlorinated organic pollutants.

No abstract

The pharmaceutical drug diclofenac (2- [(2,6-dichlorophenyl)amino]benzeneacetic acid) was detected in rivers and lakes in Switzerland. The data strongly suggest inputs of diclofenac from human medical use via wastewater treatment plants. Interestingly, the concentrations in a major tributary to a lake (Greifensee) were significantly higher (up to 370 ng/L) than those in the outflow of this lake (up to 12 ng/L). It is estimated that more than 90% of the diclofenac entering the lake is eliminated in the lake, most likely by photolytic degradation. Diclofenac was not detected in the sediments of the lake, and in a laboratory experiment, it showed negligible adsorption onto sediment particles. Incubation of lake water, fortified with diclofenac, showed no degradation in the dark, suggesting minimal chemical and biological degradation. However, when the fortified water was exposed to sunlight, rapid photodegradation was observed with a (pseudo) first-order kinetic and a half-life of less than 1 h (October and 47°N latitude). Modeling these experimental data for the situation of Greifensee, the data indicated that photodegradation can account for the rapid elimination of diclofenac in the lake. Several photoproducts were characterized in the laboratory experiments but were so far not detected under the natural conditions in the lake. Whereas photodegradation is often one among several degradation pathways for environmental contaminants, the photolysis experiments and the computer simulation suggested this process to be the predominant one for diclofenac in the lake.

Chiral pesticides are often degraded enantio-/stereoselectively in soils. Degradation is typically studied with one or a small number of soils so that it is not possible to extrapolate the findings on chiral preference to other soils. For this study, the fungicide metalaxyl was chosen as a "chiral probe" to investigate its enantioselective degradation in 20 different soils, selected primarily to cover a wide range of soil properties (e.g., acidic/alkaline, aerobic/ anaerobic) rather than to consider soils of agricultural importance. Racemic metalaxyl was incubated in these soils under laboratory conditions, and the degradation of the enantiomers as well as the enantioselective formation/ degradation of the primary major metabolite, metalaxyl acid, was followed over time, using enantioselective GC-MS after ethylation with diazoethane. In aerobic soils with pH > 5, the fungicidally active R-enantiomer was degraded faster than the S-enantiomer (k(R) > k(S)), leading to residues with a composition [S] > [R]. However, in aerobic soils with pH 4-5, both enantiomers were degraded at similar rates (k(R) approximately k(S)), and in aerobic soils with pH < 4 and in most anaerobic soils, the enantioselectivity was reversed (k(R) < k(S)). These considerable soil-to-soil variations were observed with soils from locations close to each other, in one case even within a single soil profile. Liming and acidification of a "nonenantioselective" soil prior to incubation resulted in enantioselective degradation with k(R)> k(S) and k(R) < k(S), respectively. While the enantioselectivity (expressed as ES = (k(R) - k(S))/(k(R) + k(S))) of metalaxyl degradation in aerobic soils apparently correlated with soil pH, no such correlation was found for metalaxyl acid. Reevaluation of published kinetic data for the herbicides dichlorprop and mecoprop indicated similar correlations between soil pH and ES as for metalaxyl.