Which way for welfare in the South Pacific?
In: International social work, Band 45, Heft 2, S. 239-250
ISSN: 1461-7234
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In: International social work, Band 45, Heft 2, S. 239-250
ISSN: 1461-7234
In: Community development journal, Band 29, Heft 3, S. 215-221
ISSN: 1468-2656
In: International social work, Band 32, Heft 1, S. 39-51
ISSN: 1461-7234
In: Community development journal, Band 24, Heft 4, S. 256-263
ISSN: 1468-2656
In: Community development journal, Band 19, Heft 1, S. 40-45
ISSN: 1468-2656
In: Environmental science and pollution research: ESPR, Band 27, Heft 22, S. 27995-28005
ISSN: 1614-7499
AbstractChemcatcher® and POCIS passive sampling devices are widely used for monitoring polar organic pollutants in water. Chemcatcher® uses a bound Horizon Atlantic™ HLB-L sorbent disk as receiving phase, whilst the POCIS uses the same material in the form of loose powder. Both devices (n = 3) were deployed for 21 days in the final effluent at three wastewater treatment plants in South Wales, UK. Following deployment, sampler extracts were analysed using liquid chromatography time-of-flight mass spectrometry. Compounds were identified using an in-house database of pharmaceuticals using a metabolomics workflow. Sixty-eight compounds were identified in all samplers. For the POCIS, substantial losses of sorbent (11–51%) were found during deployment and subsequent laboratory analysis, necessitating the use of a recovery factor. Percentage relative standard deviations varied (with 10 compounds exceeding 30% in both samplers) between individual compounds and between samplers deployed at the three sites. The relative performance of the two devices was evaluated using the mass of analyte sequestered, measured as an integrated peak area. The ratio of the uptake of the pharmaceuticals for the POCIS versus Chemcatcher® was lower (1.84x) than would be expected on the basis of the ratio of active sampling areas (3.01x) of the two devices. The lower than predicted uptake may be attributable to the loose sorbent material moving inside the POCIS when deployed in the field in the vertical plane. In order to overcome this, it is recommended to deploy the POCIS horizontally inside the deployment cage.
In: Environmental science and pollution research: ESPR, Band 30, Heft 7, S. 17965-17983
ISSN: 1614-7499
Abstract
The River Itchen and River Test, two chalk streams in Southern England, are sites of special scientific interest. These ecosystems face a number of environmental pressures from anthropogenic inputs of organic pollutants. Hence, we investigated the occurrence of these chemicals within the two catchments. Spot water samples (1 L) were collected at nineteen sites along the catchment on two occasions (March and June 2019). Samples were extracted (HLB-L sorbent disks) and analysed using high-resolution liquid chromatography-quadrupole-time-of-flight mass spectrometry and gas chromatography-mass spectrometry. Compounds were identified against commercially available databases. Using this approach, we found 115 pharmaceutical and personal care products, 81 plant protection products and 35 industrial chemicals. This complex mixture of pollutants covered a range of physico-chemical properties and included priority substances in the EU Water Framework Directive or currently on the third Watch List. Both rivers had similar chemical profiles for both months. Herbicides and fungicides were dominant in the spring, whereas insecticides occurred more frequently in the summer. Point discharges from wastewater treatment plants were the main source of pharmaceutical and personal care products. Agricultural activities were the main contributor to the presence of plant protection products. The impact of these organic chemicals on the ecology, particularly on macroinvertebrate biodiversity, is unknown and warrants further investigation. Our suspect screening approach could guide future toxicological investigations to assess the environmental impacts of these diverse chemicals.
In: Allan , I , Vrana , B , Greenwood , R , Mills , G , Roig , B & Gonzalez , C 2005 , ' Water quality monitoring: a 'toolbox' in response to the EU's Water Framework Directive requirements ' International Environmental Technology .
The Water Framework Directive (WFD, 2000/60/EC) is one of the most important pieces of environmental legislation produced in recent years and is likely to transform the way water quality monitoring is undertaken across all European Union's member states. The objectives of the WFD are to improve, protect and prevent further deterioration of quality for most types of water body across Europe. The Directive aims to achieve and ensure "good quality" status of all water bodies throughout Europe by 2015, and this is to be achieved by implementing management plans at the river basin level. Monitoring is required to cover a number of 'water quality elements' including biological, chemical (inorganic and organic priority pollutants), hydro-morphological, and physicochemical parameters. Three modes of monitoring regime are specified in the Directive and will form part of the management plans that must be introduced by December 2006. These include: (i) surveillance monitoring aimed at assessing long-term water quality changes and providing baseline data on river basins allowing the design and implementation of other types of monitoring, (ii) operational monitoring aimed at providing additional and essential data on water bodies at risk or failing environmental objectives of the WFD, (iii) investigative monitoring aimed at assessing causes of such failure when they are unknown.
BASE
In: Petrie , B , Gravell , A , Mills , G A , Youdan , J , Barden , R & Kasprzyk-Hordern , B 2016 , ' In situ calibration of a new Chemcatcher configuration for the determination of polar organic micropollutants in wastewater effluent ' Environmental Science & Technology , vol 50 , no. 17 , pp. 9469-9478 . DOI:10.1021/acs.est.6b02216
Passive sampling is proposed as an alternative to traditional grab- and composite-sampling modes. Investigated here is a novel passive sampler configuration, the Chemcatcher containing an Atlantic HLB disk covered by a 0.2 μm poly(ether sulfone) membrane, for monitoring polar organic micropollutants (personal care products, pharmaceuticals, and illicit drugs) in wastewater effluent. In situ calibration showed linear uptake for the majority of detected micropollutants over 9 days of deployment. Sampling rates (RS) were determined for 59 compounds and were generally in the range of 0.01–0.10 L day–1. The Chemcatcher was also suitable for collecting chiral micropollutants and maintaining their enantiomeric distribution during deployment. This is essential for their future use in developing more accurate environmental risk assessments at the enantiomeric level. Application of calibration data in a subsequent monitoring study showed that the concentration estimated for 92% of micropollutants was within a factor of 2 of the known concentration. However, their application in a legislative context will require further understanding of the properties and mechanisms controlling micropollutant uptake to improve the accuracy of reported concentrations.
BASE
Passive sampling is proposed as an alternative to traditional grab- and composite-sampling modes. Investigated here is a novel passive sampler configuration, the Chemcatcher containing an Atlantic HLB disk covered by a 0.2μm poly(ether sulfone) membrane, for monitoring polar organic micropollutants (personal care products, pharmaceuticals and illicit drugs) in wastewater effluent. In situ calibration showed linear uptake for the majority of detected micropollutants over 9 days of deployment. Sampling rates (RS) were determined for 59 compounds and were generally in the range of 0.01−0.10 L day−1. The Chemcatcher was also suitable for collecting chiral micropollutants and maintaining their enantiomeric distribution during deployment. This is essential for their future use in developing moreaccurate environmental risk assessments at the enantiomeric level. Application of calibration data in a subsequent monitoring study showed that the concentration estimated for 92% of micropollutants was within a factor of 2 of the known concentration. However, their application in a legislative context will require further understanding of the properties and mechanisms controlling micropollutant uptake to improve the accuracy of reported concentrations.
BASE
In: Cole , R , Mills , G , Bakir , A , Townsend , I , Gravell , A & Fones , G R 2016 , ' A simple, low cost GC/MS method for the sub-nanogram per litre measurement of organotins in coastal water ' MethodsX , vol 3 , pp. 490-496 . DOI:10.1016/j.mex.2016.07.001
Tributyltin (TBT) is a legacy pollutant in the aquatic environment, predominantly from its use in anti-foulant paints and is listed as a priority hazardous substance in the European Union's Water Framework Directive (WFD). Measuring low concentrations of TBT and other organotins (e.g. monobutyltin (MBT), dibutyltin (DBT), diphenyltin (DPhT) and triphenyltin (TPhT)) at sub ng/L concentrations in coastal waters using standard laboratory instrumentation is very challenging. Conventional, low injection volume gas chromatography/mass spectrometry (GC/MS) combined with liquid-liquid extraction typically achieves limits of detection for TBT ∼10 ng L−1. We describe a simple, programmed temperature vaporisation-large injection volume (50 μL), GC/MS selected ion monitoring method for measuring DBT, TBT, DPhT and TPhT in coastal waters at lower concentrations. Quantification of MBT was not possible using these injection volumes but was achieved using a 10 μL injection volume together with a reduced injection speed.This new approach offers:• When using a 50 μL injection, limits of detection = 0.70 ng L−1 and limits of quantification = 2.1 ng L−1 for TBT were achieved in derivatised standards.• Recoveries of TBT and TPhT from coastal water >97%.• Time consuming, off-line sample pre-concentration methods are unnecessary.
BASE
Tributyltin (TBT) is a legacy pollutant in the aquatic environment, predominantly from its use in anti-foulant paints and is listed as a priority hazardous substance in the European Union's Water Framework Directive (WFD). Measuring low concentrations of TBT and other organotins (e.g. monobutyltin (MBT), dibutyltin (DBT), diphenyltin (DPhT) and triphenyltin (TPhT)) at sub ng/L concentrations in coastal waters using standard laboratory instrumentation is very challenging. Conventional, low injection volume gas chromatography/mass spectrometry (GC/MS) combined with liquid-liquid extraction typically achieves limits of detection for TBT ∼10 ng L−1. We describe a simple, programmed temperature vaporisation-large injection volume (50 μL), GC/MS selected ion monitoring method for measuring DBT, TBT, DPhT and TPhT in coastal waters at lower concentrations. Quantification of MBT was not possible using these injection volumes but was achieved using a 10 μL injection volume together with a reduced injection speed.
BASE
In: Environmental science and pollution research: ESPR, Band 25, Heft 25, S. 25130-25142
ISSN: 1614-7499
In: AEAOA-D-22-00015
SSRN