Toxins in cyanobacteria are a recognized risk in the treatment of drinking-water treatment. Cyanotoxins can occur in two modifications: cell bound and dissolved in water. The process of toxin release may occur naturally, but it also may be induced through the processes of drinking-water treatment. Both causes of release are relevant to the safety of drinking water. This study investigated cyanotoxin release and elimination through different treatment trains in systematic pilot-scale studies with water from the Weida Reservoir, in Thuringia, Germany. The Weida Reservoir is a dimictic mesoeutrophic reservoir typical for a number of mountainous areas in Europe, with Planktothrix rubescens as the dominant phytoplankton species, and shows a characteristic seasonal pattern of population development and microcystin occurrence. To assess the risk of microcystin breakthrough, the pilot-scale results as well as results of laboratory-scale experiments were used for developing a kinetic model of toxin release in relation to elimination. By calculating removal efficiency of total microcystins (cell bound and dissolved) for different treatment trains, raw water quality was related to the quality targets for finished water, and breakthrough risks could be calculated for given treatment trains and varying cyanobacterial population densities in the reservoir.
Cyanobacterial neurotoxins, such as anatoxin-a and saxitoxin, as well as hepatotoxins including microcystins and noclularin were simultaneously determined in water samples by ion-pair supported, solid phase extraction (SPE) and reversed-phase liquid chromatography coupled to UV and tandem mass spectrometry (RP-LC-UV; MS-MS). With quantification limits in water 1 samples of approximately 50 ng L for the microcystins (MC-LR, -YR, -RR, -LA), noclularin, and 1 anatoxin-a and 630 ng L for saxitoxin the method is well suited for surveillance of the proposed WHO guidelines for cyanobacterial toxins. MS detection permits, unlike the commonly used UV cletection, unambiguous identification and accurate quantification of cyanobacterial toxins even in highly matrix-polluted, watersamples.
The indicator function of the fluorescence signals of the cyanopigments phycocyanin and phycoerythrin as early warning parameters against the microcystins in drinking water was investigated by lab- and pilot-scale studies. The early warning function of the fluorescence signals was examined with regard to the signals' real-time character, their sensitivity and the behaviour of the cyanopigments in different treatment stages in comparison to microcystins. Fluorescence measurements confirmed the real-time character, since they can be carried out on-site without the pre-concentration of pigments. The limit of detection of phycoerythrin is determined at 0.7 microg/L and of phycocyanin at 5.3 microg/L respectively. If the pigment/microcystin ratio is known and calculated to be higher than 1, very low microcystin concentrations can be estimated by the fluorescence signals. The compared behaviour of both pigments and selected microcystins (MC-LR and MC-RR) during water treatment shows that pigments have an early warning function against microcystins in conventional treatment stages using pre-oxidation with permanganate, powdered-activated carbon and chlorination. In contrast, cyanopigments do not have an early warning function if chlorine dioxide is used as a pre-oxidant or final disinfection agent. In order to use pigment control measurements in drinking water treatment the initial pigment/toxin ratio of the raw water must be known.
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