An enantioselective study of the behavior of the herbicide ethofumesate in agricultural soils: Impact of the addition of organoclays and biochar.

Chiral pesticides that are still commercialized and incorporated into the environment as racemic mixtures of enantiomers require evaluation of the enantioselectivity of their biological activity and environmental fate processes for a better prediction of their field efficacy and environmental risks. In this work, we successfully separated the enantiomers of the chiral herbicide ethofumesate (ETFM), determined their absolute configuration, and characterized their herbicidal activity as well as their adsorption, degradation, enantiomerization, and leaching in Mediterranean agricultural soils. While the herbicidal activity of R-ethofumesate to the sensitive species Portulaca grandiflora was greater than that of S-ethofumesate, the adsorption, degradation, and leaching of the herbicide showed negligible enantioselectivity and enantiomer interconversion did not occur in soils.

Soil Effects on the Bioactivity of Hydroxycoumarins as Plant Allelochemicals.

Soil plays a primary role in the activity of plant allelochemicals in natural and agricultural systems. In this work, we compared the phytotoxicity of three natural hydroxycoumarins (umbelliferone, esculetin, and scopoletin) to different model plant species (, , and ) in Petri dishes, and then selected the most phytotoxic compound (umbelliferone) to assess how its adsorption and dissipation in two distinct soils affected the expression of its phytotoxic activity. The root growth inhibitory effect of umbelliferone was significantly greater than that of esculetin and scopoletin, and the dicot species ( and ) were more sensitive to the hydroxycoumarins than the monocot species ().

Sorption and dissipation of the allelochemicals umbelliferone and salicylic acid in a Mediterranean soil environment: Effect of olive-mill waste addition.

Allelochemicals are receiving much attention as natural alternatives to synthetic pesticides. Very little is known, however, about the processes to which allelochemicals are subjected once they reach the soil environment, despite the fact that it is widely recognized that such processes can dramatically influence their bioactivity and applicability as eco-friendly pesticides. The objectives of this study were to characterize the sorption and dissipation of two phenolic allelochemicals, umbelliferone (UM) and salicylic acid (SA), after their simultaneous application to a Mediterranean agricultural soil and to assess to what extent sorption and dissipation were affected by amending the soil with an agro-industrial organic waste (olive-mill waste, OMW), as a common agronomic practice in Mediterranean agricultural systems.

Nanoengineered Sorbents To Increase the Persistence of the Allelochemical Carvone in the Rhizosphere.

This study investigates the changes in sorption/desorption, dissipation, and leaching of the two enantiomeric forms of the allelochemical carvone, R-carvone and S-carvone, after amending an agricultural soil sample with two nanoengineered sorbents: biochar (BC) and organoclay (OCl). The sorption of carvone enantiomers was nonenantioselective and similarly improved by the addition of OCl and BC to the soil. However, OCl-amended soil showed reversible sorption, whereas BC-amended soil displayed sorption-desorption hysteresis.

Evidence for the effect of sorption enantioselectivity on the availability of chiral pesticide enantiomers in soil.

Although enantioselective sorption to soil particles has been proposed as a mechanism that can potentially influence the availability of individual chiral pesticide enantiomers in the environment, environmental fate studies generally overlook this possibility and assume that only biotic processes can be enantioselective, whereas abiotic processes, such as sorption, are non-enantioselective. In this work, we present direct evidence for the effect of the enantioselective sorption of a chiral pesticide in a natural soil on the availability of the single pesticide enantiomers for transport. Batch sorption experiments, with direct determination of the sorbed amounts, combined with column leaching tests confirmed previous observations that from non-racemic aqueous solutions the sorption of the chiral fungicide metalaxyl on the soil appeared to be enantioselective, and further demonstrated that the enantiomer that was sorbed to a greater extent (R-metalaxyl, Kd = 1.

Enantioselective sorption of the chiral fungicide metalaxyl on soil from non-racemic aqueous solutions: Environmental implications.

Mechanisms governing the enantioselectivity of the processes that determine the behavior of chiral pollutants in the environment need to be better understood. Understanding these mechanisms should help improve predictions of the hazards and risks chiral compounds can pose to people and the environment. We report the results of batch sorption experiments indicating that the sorption of the chiral fungicide metalaxyl on soil from non-racemic initial solutions was enantioselective.

Selective modification of clay minerals for the adsorption of herbicides widely used in olive groves.

Ground and surface water contamination by herbicides applied to olive groves in Spain and other Mediterranean countries is demanding strategies to prevent and remediate the environmental problems repeatedly caused by such herbicides. In this study, six different organic cations (L-carnitine, spermine, hexadimethrine, tyramine, phenyltrimethylammonium, and hexadecyltrimethylammonium) were incorporated into Na-rich Wyoming montmorillonite (SWy-2) and Ca-rich Arizona montmorillonite (SAz-1) at two different loadings (50% and 100% of the cation exchange capacity of the clays) as a strategy to enhance the affinity of the clay minerals for three herbicides widely used in olive groves: terbuthylazine, diuron, and MCPA. The modified montmorillonites were characterized and tested as adsorbents of the herbicides through batch adsorption tests.