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Pesticide Fate and Transport throughout Unsaturated Zones in Five Agricultural Settings, USA
Author(s) -
Hancock Tracy C.,
Sandstrom Mark W.,
Vogel Jason R.,
Webb Richard M.T.,
Bayless E. Randall,
Barbash Jack E.
Publication year - 2008
Publication title -
journal of environmental quality
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.888
H-Index - 171
eISSN - 1537-2537
pISSN - 0047-2425
DOI - 10.2134/jeq2007.0024
Subject(s) - metolachlor , atrazine , alachlor , acetochlor , groundwater recharge , pesticide , vadose zone , environmental chemistry , hydrology (agriculture) , chemistry , surface water , environmental science , soil water , water pollution , groundwater , aquifer , agronomy , environmental engineering , soil science , geology , geotechnical engineering , biology
Pesticide transport through the unsaturated zone is a function of chemical and soil characteristics, application, and water recharge rate. The fate and transport of 82 pesticides and degradates were investigated at five different agricultural sites. Atrazine and metolachlor, as well as several of the degradates of atrazine, metolachlor, acetochlor, and alachlor, were frequently detected in soil water during the 2004 growing season, and degradates were generally more abundant than parent compounds. Metolachlor and atrazine were applied at a Nebraska site the same year as sampling, and focused recharge coupled with the short time since application resulted in their movement in the unsaturated zone 9 m below the surface. At other sites where the herbicides were applied 1 to 2 yr before sampling, only degradates were found in soil water. Transformations of herbicides were evident with depth and during the 4‐mo sampling time and reflected the faster degradation of metolachlor oxanilic acid and persistence of metolachor ethanesulfonic acid. The fraction of metolachlor ethanesulfonic acid relative to metolachlor and metolachlor oxanilic acid increased from 0.3 to >0.9 at a site in Maryland where the unsaturated zone was 5 m deep and from 0.3 to 0.5 at the shallowest depth. The flux of pesticide degradates from the deepest sites to the shallow ground water was greatest (3.0–4.9 μmol m −2 yr −1 ) where upland recharge or focused flow moved the most water through the unsaturated zone. Flux estimates based on estimated recharge rates and measured concentrations were in agreement with fluxes estimated using an unsaturated‐zone computer model (LEACHM).