Abstract

SummaryMCPA was weakly absorbed in soils with 2.4, 3.0 and 2.9% humus. Kd‐values were 0.7, 0.9 and 1.0, respectively. In soil, not previously treated with MCPA, the degradation of 0.05 mg kg−114C‐MCPA followed first‐order reaction kinetics whereas degradation of 5 mg kg−1 was only first‐order for 2 weeks; exponentially increasing degradation rates followed indicating enrichment of the soil with MCPA decomposers. Degradation was monitored by evolution of 14CO2. The influence of temperature on degradation of MCPA (4 mg kg−1) could initially be described by Q10 values or by the Arrhenius equation. After 1 day of incubation in two field soils Q10 values were 3.3 and 2.9, respectively, between 0°C and 29°C; the activation energies were 87 and 76 kj mol−1. Exponentially increasing degradation rates followed with doubling times of about 4.0, 1.8, 1.2 and 0.6 days at 6,10, 15 and 21°C, respectively. After 51 days of incubation, at temperatures between 6°C and 29°C, about 60%14C was evolved in CO2 and only traces of MCPA were left in the soil. At 0°C and at 40°C only 1% and 10%14C, respectively, were evolved as CO2 after 51 days. 14C‐MCPA (4 mg kg−1) was incubated at moisture contents from that in air‐dried soil to 2.3 times field capacity. Optimum for degradation was from 0.6 to 1.2. field capacity. Degradation was very slow where water contents were below the level of wilting point and was nil in air‐dried soil. In wet soil degradation was delayed, but even in water‐logged soil (2.3 times field capacity) MCPA was decomposed after 4 to 5 weeks at 10°C.

Full Text
Paper version not known

Talk to us

Join us for a 30 min session where you can share your feedback and ask us any queries you have

Schedule a call

Disclaimer: All third-party content on this website/platform is and will remain the property of their respective owners and is provided on "as is" basis without any warranties, express or implied. Use of third-party content does not indicate any affiliation, sponsorship with or endorsement by them. Any references to third-party content is to identify the corresponding services and shall be considered fair use under The CopyrightLaw.