4.5 Article

Local and regional sources of organochlorine pesticides in a rural zone in central Chile

Journal

ATMOSPHERIC POLLUTION RESEARCH
Volume 13, Issue 5, Pages -

Publisher

TURKISH NATL COMMITTEE AIR POLLUTION RES & CONTROL-TUNCAP
DOI: 10.1016/j.apr.2022.101411

Keywords

Organochlorine pesticides; Atmosphere; Agriculture; PUF-PAS; Central Chile; Backward wind trajectories

Funding

  1. Agencia Nacional de Investigacion y Desarrollo (ANID) [FONDAP 15130011, FONDAP 15110020, REDES 180078, FONDECYT 1211931]
  2. Vicerr Pontificia Universidad Catolica de Chile [9/2014]
  3. Pontificia Universidad Catolica de Chile
  4. Iowa Superfund Basic Research Program, National Institute of Environmental Health Sciences [P42ES013661]
  5. Ministry of Education, Youth and Sports [LM2018121]
  6. Operational Programme Research, Develop-ment and Education (CETOCOEN EXCELLENCE project) [CZ.02.1.01/0.0/0.0/17_043/0009632]
  7. European Union [857560]

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This study is the first one to measure the spatiotemporal variation of airborne organochlorinated pesticides (OCPs) in a major agriculture area in Central Chile. The results showed that the concentrations of OCPs were influenced by soil volatilization and waste burning, and most OCP concentrations exhibited significant spatial heterogeneity, while some concentrations depended on regional sources.
There is a lack of knowledge about exposure to airborne organochlorinated pesticides (OCPs), especially for people living near agricultural zones in developing countries. This study is the first one to measure spatiotemporal variation of airborne OCPs within a major agriculture area in Central Chile. Polyurethane foam passive air samplers (PUF-PAS) were deployed in five sites in the town of Molina (35 degrees 7'S, 71 degrees 17'W) and another one in the nearby town of Lontue (35 degrees 3'S, 71 degrees 17'W). Samplers were deployed from August 2016 to January 2018, in 8 periods lasting 2-3 months each. The measured concentrations in air (pg m(-3)) as geometric mean were alpha-HCH: 0.59, gamma-HCH: 3.8, o,p LDDT: 1.3, p,p'-DDT: 2.0, o,p'-DDE: 0.52, p,p '-DDE: 5.5, o,p'-DDD: 0.26, p,p'-DDD: 0.64, PeCB: 29.1 and HCB: 14.5. The highest concentrations were measured in the warmer months and negative correlations (p < 0.05) between the log of the concentrations and the inverse of ambient temperature were found, suggesting soil volatilization as the main release process. The exceptions were o,p'-DDE, p,p '-DDE and HCB. In the case of HCB, waste burning was a likely source. Most OCP concentrations showed significant spatial heterogeneity (p < 0.05), suggesting local source contributions are dominant; the exceptions are alpha-HCH and PeCB (p > 0.05) whose concentrations depend on regional sources. Backward wind trajectories obtained using NOAA's HYSPLIT identified air masses coming from the south and southwest when ambient concentrations are highest; these regional sources contribute to all ambient OCP concentrations.

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