Atmospheric deposition of semivolatile organic pollutants in European high mountains: Sources, settling and chemical degradation

Bulk atmospheric deposition samples, including wet and dry deposition, were collected during 2004–2006 in four high mountain European lakes: Skalnate Pleso (Tatra mountains, Slovakia), Gossenköllesee (Alps, Austria), Redon (Pyrenees, Spain) and Lochnagar (Grampian Mountains, Scotland). Samples were...

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Detalles Bibliográficos
Autores: Fernández Ramón, M. Pilar, Van Drooge, Barend L., Arellano, Lourdes, Grimalt, Joan O.
Tipo de recurso: artículo
Estado:Versión aceptada para publicación
Fecha de publicación:2021
País:España
Institución:Consejo Superior de Investigaciones Científicas (CSIC)
Repositorio:DIGITAL.CSIC. Repositorio Institucional del CSIC
OAI Identifier:oai:digital.csic.es:10261/238798
Acceso en línea:http://hdl.handle.net/10261/238798
Access Level:acceso abierto
Palabra clave:Photochemical degradation
Persistent organic pollutants
Wet and dry deposition
Long-range atmospheric transport
Descripción
Sumario:Bulk atmospheric deposition samples, including wet and dry deposition, were collected during 2004–2006 in four high mountain European lakes: Skalnate Pleso (Tatra mountains, Slovakia), Gossenköllesee (Alps, Austria), Redon (Pyrenees, Spain) and Lochnagar (Grampian Mountains, Scotland). Samples were analysed for polycyclic aromatic hydrocarbons (PAHs), polychlorobiphenyls (PCBs), hexachlorobenzene (HCB), hexachlorocyclohexanes (HCHs), endosulfans, and polybromodiphenyl ethers (PBDEs). The deposition of PCBs, HCHs, and low brominated BDEs reflected baseline contributions from long range atmospheric transport. This was also the case for PAHs in Redon and Gossenköllesee, endosulfans in Lochnagar and Gossenköllesee and HCB in these three lakes. However, Skalnate received PAHs, endosulfans and HCB from regional sources as it was the case for endosulfans in Redon. The distinct origin of these pollutants was reflected in the relative composition of some metabolites such as the proportion of endosulfan sulfate vs α- and β-endosulfans or the relative composition of BDE47 and BDE99. Wet deposition was the main process for atmospheric removal of PAHs, HCHs and HCB. In addition, warm season revolatilization from soils and melting snow with subsequent condensation at low temperature were significant for volatile PAHs, HCB, low chlorinated PCBs and endosulfans. Reaction with OH radicals was not a significant loss process of HCHs and HCB in remote areas, dominated by wet deposition, whereas. PCBs and PAHs were significantly removed by both wet deposition and OH radical oxidation, the latter dominating in the highest altitude sites. Photolysis was the main atmospheric removal process of PBDEs, which dominates over atmospheric deposition and OH depletion in all sites.