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The Effect of High 2,4‐D Concentrations on Degradation and Carbon Dioxide Evolution in Soils
Author(s) -
Ou LiTse,
Rothwell D. F.,
Wheeler W. B.,
Davidson J. M.
Publication year - 1978
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/jeq1978.00472425000700020018x
Subject(s) - loam , soil water , carbon dioxide , degradation (telecommunications) , environmental chemistry , chemistry , incubation , total organic carbon , carbon fibers , soil science , mineralogy , environmental science , materials science , organic chemistry , telecommunications , biochemistry , composite number , computer science , composite material
A laboratory experiment was conducted to determine the degradation of high concentrations of 2,4‐D (2,4‐dichlorophenoxyacetic acid) and CO 2 evolution in three soils. Two forms of 2,4‐D, technical grade and formulated, were added to each soil at rates of 50, 500, 5,000 and 20,000 µ g/g of soil (ppm). Degradation of the 2,4‐D was measured by 14 CO 2 evolution resulting from the oxidation of uniformly ringlabeled carbon. At an application rate of 500 ppm, all three soils degraded 2,4‐D. At 5,000 and 20,000 ppm, degradation occurred in the Webster silty clay loam and Terra Ceia organic soil, but not in the Cecil sandy loam during 80 days of incubation. The degradation rate was generally higher for the formulated 2,4‐D than the technical grade material. For the higher 2,4‐D concentrations, 5,000 or 20,000 ppm, when extensive degradation occurred, total CO 2 evolution was also greatly stimulated, and the pattern of total CO 2 evolution rate exhibited a two‐peak response. Carbon dioxide‐carbon (CO 2 ‐C) from the first peak appeared to be mainly from the formulation materials or from the impurities and CO 2 ‐C from the second peak was mainly from 2,4‐D‐C.