Seasonality of enteric viruses in groundwater-derived public water sources.

We investigated the seasonal prevalence of seven enteric viruses in groundwater-derived public water sources distributed across the dominant aquifers of England. Sampling targeted four periods in the hydrological cycle with typically varying microbial risks, as indicated using a decade of Escherichia coli prevalence data. Viruses were concentrated onsite by filtration of raw groundwater, and extracted nucleic acid (NA) was amplified by qPCR or RT-qPCR. Seven out of eight sources, all aquifers, and 31% of samples were positive for viral NA. The most frequently detected viral NA targets were Hepatitis A virus (17% samples, 63% sites), norovirus GI (14% samples, 38% sites), and Hepatitis E virus (7% samples, 25% sites). Viral NA presence was episodic, being most prevalent and at its highest concentration during November and January, the main groundwater recharge season, with 89% of all positive detects occurring during a rising water table. Seasonal norovirus NA detections matched its seasonal incidence within the population. Viral NA is arriving with groundwater recharge, as opposed to persisting for long-periods within the saturated zone. Neither total coliforms nor E. coli were significant predictors of viral NA presence-absence, and there was limited co-occurrence between viruses. Nevertheless, a source with an absence of E. coli in regularly collected historical data is unlikely to be at risk of viral contamination. To manage potential groundwater viral contamination via risk assessment, larger scale studies are required to understand key risk factors, with the evidence here suggesting viral NA is widespread across a range of typical microbial risk settings.

Provenance of drinking water revealed through compliance sampling.

Understanding drinking water hydrochemistry is essential for maintaining safe drinking water supplies. Whilst targeted research surveys have characterised drinking water hydrochemistry, vast compliance datasets are routinely collected but are not interrogated amidst concerns regarding the impact of mixed water sources, treatment, the distribution network and customer pipework. In this paper, we examine whether compliance samples retain hydrochemical signatures of their provenance. We first created and subsequently undertook the first hydrochemical analysis of a novel national database of publically available drinking water compliance analyses (n = 3 873 941) reported for 2015 across England and Wales. k-means cluster analysis revealed three spatially coherent clusters. Cluster 1 is dominated by groundwater sources, with high nitrate concentrations and mineralisation, and lower organic carbon, residual chlorine and THM formation. Cluster 2 was dominated by surface water sources and characterised by low mineralisation (low conductivity and major ion concentrations), low nitrate and high organic carbon concentrations (and hence residual chlorine and THM formation). Cluster 3 shows a mixture of groundwater overlain by confining layers and superficial deposits (resulting in higher trace metal concentrations and mineralisation) and surface water sources. These analyses demonstrate that, despite extensive processing of drinking water, at the national scale signatures of the provenance of drinking water remain. Analysis of compliance samples is therefore likely to be a helpful tool in the characterisation of processes that may affect drinking water chemistry. The methodology used is generic and can be applied in any area where drinking water chemistry samples are taken.

Fingerprinting groundwater pollution in catchments with contrasting contaminant sources using microorganic compounds.

Evaluating the occurrence of microorganics helps to understand sources and processes which may be controlling the transport and fate of emerging contaminants (ECs). A study was carried out at the contrasting instrumented environmental observatory sites at Oxford, on the peri-urban floodplain gravel aquifer of the River Thames and Boxford, in the rural valley of the River Lambourn on the chalk aquifer, in Southern England to explore the use of ECs to fingerprint contaminant sources and flow pathways in groundwater. At Oxford compounds were typical of a local waste tip plume (not only plasticisers and solvents but also barbiturates and N,N-diethyl-m-toluamide (DEET)) and of the urban area (plasticisers and mood-enhancing drugs such as carbamazepine). At Boxford the results were different with widespread occurrence of agricultural pesticides, their metabolites and the solvent trichloroethene, as well as plasticisers, caffeine, butylated food additives, DEET, parabens and trace polyaromatic hydrocarbons (PAHs). Groups of compounds used in pharmaceuticals and personal care products of different provenance in the environment could be distinguished, i) historical household and medical waste, ii) long-term household usage persistent in groundwater and iii) current usage and contamination from surface water. Co-contaminant and degradation products can also indicate the likely source of contaminants. A cocktail of contaminants can be used as tracers to provide information on catchment pathways and groundwater/surface water interactions. A prominent feature in this study is the attenuation of many EC compounds in the hyporheic zone.