Field experiments were conducted on six loam and sandy loam soils to study the influence of various soil parameters on atrazine, cyanazine, alachlor, metolachlor, and pendimethalin efficacy. Herbicidal activity was highly correlated to the soil organic content. Humic matter content was equally or better correlated (r = 0.70 to 0.91) with herbicide bioactivity than was organic matter content (r = 0.66 to 0.84). Regression equations were determined which allow herbicide rate recommendations for 80% weed control to be calculated based on soil humic matter or organic matter levels.

Aqueous batch-type sorption-desorption studies and soil column leaching studies were conducted to determine the influence of soil properties, soil and suspension pH, and ionic concentration on the retention, release, and mobility of [14C]imazaquin in Cape Fear sandy clay loam, Norfolk loamy sand, Rion sandy loam, and Webster clay loam. Sorption of [14C]metolachlor was also included as a reference standard. L-type sorption isotherms, which were well described by the Freundlich equation, were observed for both compounds on all soils. Metolachlor was sorbed to soils in amounts 2-8 times that of imazaquin, and retention of both herbicides was related to soil organic matter (OM) and humic matter (HM) contents and to herbicide concentration. Metolachlor retention was also related to soil clay content. Imazaquin sorption to one soil (Cape Fear) increased as concentration increased and as suspension pH decreased, with maximum sorption occurring in the vicinity of pK(a1) = (1.8). At pH levels below pK(a1) imazaquin sorption decreased as hydronium ions (H3O+) increased and competed for sites. NaCl was more effective than water in desorption of imazaquin at pH levels near the pK(a1). Mechanisms of bonding are postulated and discussed. The mobility of imazaquin through soil columns was in the order Rion > or = Norfolk > Cape Fear > or = Webster, whereas for metolachlor it was Rion > or = Norfolk >> Webster > or = Cape Fear. Imazaquin was from 2 to 10 times as mobile as metolachlor.

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