The biogeochemistry of arsenic in a remote UK upland site: trends in rainfall and runoff, and comparisons with urban rivers

Rowland, A.P.; Neal, C.; Reynolds, B.; Jarvie, H.P. ORCID: https://orcid.org/0000-0002-4984-1607; Sleep, D. ORCID: https://orcid.org/0009-0002-1128-1883; Lawlor, A.J.; Neal, M.. 2011 The biogeochemistry of arsenic in a remote UK upland site: trends in rainfall and runoff, and comparisons with urban rivers. Journal of Environmental Monitoring, 13 (5). 1255-1263. 10.1039/C0EM00772B

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Abstract/Summary

Ten years of monitoring of rainfall and streams in the remote acidic and acid sensitive moorland and afforested moorland of upland mid-Wales reveals concentrations of arsenic (As) typically < 1µg L-1. On average, the lowest concentrations occur within rainfall and they have declined over time probably in response to reductions in global emissions. There is a corresponding reduction within the streams except for forested systems where concentrations up to doubled following clear-fell. Within the streams there is both annual and diurnal cycling of As. The annual cycling gives maxima during the summer months and this probably reflects the importance of groundwater inputs and mineralisation/desorption from the surface soil layers. Correspondingly, the diurnal cycling occurs during the summer months at low flow periods with As concentrations highest in the afternoon/evening. For the urban/industrial basins of northern England with historically a much higher As deposition, land contamination and effluent discharges, comparative data indicates As concentrations around three fold higher: strong seasonal patterns are observed for the same reasons as with the uplands. Across the sites, the As concentrations are over an order of magnitude lower than that of environmental concern. Nonetheless, the results clearly show the effects of declining emissions on rainfall deposition and some indication of areas of historic contamination. Arsenic is mainly present in the less than <0.45 fraction, but cross-flow filtration indicates that approx 43% is in the colloidal phase at the clean water sites, and 16% in the colloidal phase at the contaminated sites. Part of this colloidal component may well be associated with organic carbon.

Item Type:	Publication - Article
Digital Object Identifier (DOI):	10.1039/C0EM00772B
Programmes:	CEH Topics & Objectives 2009 - 2012 > Biogeochemistry > BGC Topic 1 - Monitoring and Interpretation of Biogeochemical and Climate Changes CEH Topics & Objectives 2009 - 2012 > Water > WA Topic 2 - Ecohydrological Processes
UKCEH and CEH Sections/Science Areas:	Shore Acreman Emmett
ISSN:	1464-0325
NORA Subject Terms:	Chemistry
Date made live:	05 May 2011 13:29 +0 (UTC)
URI:	https://nora.nerc.ac.uk/id/eprint/13860

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