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      Comparison of different monitoring methods for the measurement of metaldehyde in surface waters

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          Abstract

          Metaldehyde is recognised as an emerging contaminant. It is a powerful molluscicide and is the active compound in many types of slug pellets used for the protection of crops. The application of pellets to land generally takes place between August and December when slugs thrive. Due to its high use and physico-chemical properties, metaldehyde can be present in the aquatic environment at concentrations above the EU Drinking Water Directive limit of 100 ng L −1 for a single pesticide. Such high concentrations are problematic when these waters are used in the production of drinking water. Being able to effectively monitor this pollutant of concern is important. We compared four different monitoring techniques (spot and automated bottle sampling, on-line gas chromatography/mass spectrometry (GC/MS) and passive sampling) to estimate the concentration of metaldehyde. Trials were undertaken in the Mimmshall Brook catchment (Hertfordshire, UK) and in a feed in a drinking water treatment plant for differing periods between 17th October and 31st December 2017. This period coincided with the agricultural application of metaldehyde. Overall, there was a good agreement between the concentrations measured by the four techniques, each providing complementary information. The highest resolution data was obtained using the on-line GC/MS. During the study, there was a large exceedance (500 ng L −1) of metaldehyde that entered the treatment plant; but this was not related to rainfall in the area. Each monitoring method had its own advantages and disadvantages for monitoring investigations, particularly in terms of cost and turn-a-round time of data.

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          The online version of this article (10.1007/s10661-019-7221-x) contains supplementary material, which is available to authorized users.

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          Most cited references28

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          Passive sampling techniques for monitoring pollutants in water

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            Development of a passive, in situ, integrative sampler for hydrophilic organic contaminants in aquatic environments.

            Increasingly it is being realized that a holistic hazard assessment of complex environmental contaminant mixtures requires data on the concentrations of hydrophilic organic contaminants including new generation pesticides, pharmaceuticals, personal care products, and many chemicals associated with household, industrial, and agricultural wastes. To address this issue, we developed a passive in situ sampling device (the polar organic chemical integrative sampler [POCIS]) that integratively concentrates trace levels of complex mixtures of hydrophilic environmental contaminants, enables the determination of their time-weighted average water concentrations, and provides a method of estimating the potential exposure of aquatic organisms to the complex mixture of waterborne contaminants. Using a prototype sampler, linear uptake of selected herbicides and pharmaceuticals with log K(ow)s < 4.0 was observed for up to 56 d. Estimation of the ambient water concentrations of chemicals of interest is achieved by using appropriate uptake models and determination of POCIS sampling rates for appropriate exposure conditions. Use of POCIS in field validation studies targeting the herbicide diuron in the United Kingdom resulted in the detection of the chemical at estimated concentrations of 190 to 600 ng/L. These values are in agreement with reported levels found in traditional grab samples taken concurrently.
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              Calibration and use of the polar organic chemical integrative sampler--a critical review.

              The implementation of strict environmental quality standards for polar organic priority pollutants poses a challenge for monitoring programs. The polar organic chemical integrative sampler (POCIS) may help to address the challenge of measuring low and fluctuating trace concentrations of such organic contaminants, offering significant advantages over traditional sampling. In the present review, the authors evaluate POCIS calibration methods and factors affecting sampling rates together with reported environmental applications. Over 300 compounds have been shown to accumulate in POCIS, including pesticides, pharmaceuticals, hormones, and industrial chemicals. Polar organic chemical integrative sampler extracts have been used for both chemical and biological analyses. Several different calibration methods have been described, which makes it difficult to directly compare sampling rates. In addition, despite the fact that some attempts to correlate sampling rates with the properties of target compounds such as log K(OW) have been met with varying success, an overall model that can predict uptake is lacking. Furthermore, temperature, water flow rates, salinity, pH, and fouling have all been shown to affect uptake; however, there is currently no robust method available for adjusting for these differences. Overall, POCIS has been applied to a wide range of sampling environments and scenarios and has been proven to be a useful screening tool. However, based on the existing literature, a more mechanistic approach is required to increase understanding and thus improve the quantitative nature of the measurements.
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                Author and article information

                Contributors
                00 44 (0)2392 842252 , gary.fones@port.ac.uk
                Journal
                Environ Monit Assess
                Environ Monit Assess
                Environmental Monitoring and Assessment
                Springer International Publishing (Cham )
                0167-6369
                1573-2959
                15 January 2019
                15 January 2019
                2019
                : 191
                : 2
                : 75
                Affiliations
                [1 ]ISNI 0000 0001 0728 6636, GRID grid.4701.2, School of Earth and Environmental Sciences, , University of Portsmouth, ; Burnaby Road, Portsmouth, PO1 3QL UK
                [2 ]ISNI 0000 0001 0728 6636, GRID grid.4701.2, School of Pharmacy and Biomedical Sciences, , University of Portsmouth, ; White Swan Road, Portsmouth, PO1 2DT UK
                [3 ]ISNI 0000 0001 0658 8800, GRID grid.4827.9, Natural Resources Wales, NRW Analytical Services, , Swansea University, ; Faraday Building, Singleton Campus, Swansea, SA2 8PP UK
                [4 ]GRID grid.421710.1, Affinity Water Ltd., ; Tamblin Way, Hatfield, Hertfordshire, AL10 9EZ UK
                [5 ]Anatune Ltd, Unit 4, Wellbrook Court, Girton Road, Cambridge, CB3 0NA UK
                Author information
                http://orcid.org/0000-0002-1999-0716
                Article
                7221
                10.1007/s10661-019-7221-x
                6333724
                30648204
                9bde5000-9591-49ec-9358-8844af6d3e58
                © The Author(s) 2019

                Open Access This article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made.

                History
                : 19 September 2018
                : 8 January 2019
                Funding
                Funded by: FundRef http://dx.doi.org/10.13039/501100000270, Natural Environment Research Council;
                Award ID: NE/L009145/1
                Award Recipient :
                Categories
                Article
                Custom metadata
                © Springer Nature Switzerland AG 2019

                General environmental science
                metaldehyde,water monitoring,drinking water,spot sampling,passive sampling,on-line gas chromatography/mass spectrometry

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