Related Experiment Video
Updated: Jan 25, 2026

Isolation of Native Soil Microorganisms with Potential for Breaking Down Biodegradable Plastic Mulch Films Used in Agriculture
Published on: May 10, 2013
Behavior of the Chiral Herbicide Imazamox in Soils: Enantiomer Composition Differentiates between Biodegradation and
Ignaz J Buerge1, Roy Kasteel1, Astrid Bächli1
1Plant Protection Chemistry , Agroscope , CH-8820 Wädenswil , Switzerland.
Abstract:
Imazamox is a chiral herbicide that, in laboratory experiments in the dark, exhibits pronounced enantioselective biodegradation in certain soils. Imazamox also shows rapid photodegradation. However, which processes are predominant in the field is not clear. We conducted a set of soil incubation experiments under natural sunlight (and corresponding dark controls), using enantioselective LC-MS/MS analysis as a probe to distinguish biodegradation and photodegradation. Under dark conditions, imazamox was degraded enantioselectively. In contrast, degradation was nonenantioselective and 2× faster when the soil was exposed to sunlight, suggesting that biodegradation (in the dark) and photodegradation (under sunlight) were the predominant degradation processes. We also investigated the effectiveness of strategies that were proposed to exclude photodegradation in field studies, covering of soil with sand or irrigation after herbicide application. The sand cover did not prevent photodegradation. On the contrary, degradation was 10× faster than in the dark and nonenantioselective. Computer simulations supported the explanation that imazamox was transported upward by capillary flow due to evaporation onto the sand surface, where it was rapidly photodegraded. Irrigation postponed but not completely prevented photodegradation. For mobile substances susceptible to photodegradation, upward transport to the soil surface thus needs to be considered when deriving rates for biodegradation from field studies.
Related Concept Videos
Naming Enantiomers
The Soil Ecosystem
Chirality
Chiral objects exhibit a sense of handedness when they interact with another chiral object. For example, our left foot can only fit in the left shoe and not in the right shoe. Achiral objects — objects that have...
Chirality in Nature
Properties of Enantiomers and Optical Activity
Racemic Mixtures and the Resolution of Enantiomers

