Tw. Speir et al., A SIMPLE KINETIC APPROACH TO DERIVE THE ECOLOGICAL DOSE VALUE, ED(50), FOR THE ASSESSMENT OF CR(VI) TOXICITY TO SOIL BIOLOGICAL PROPERTIES, Soil biology & biochemistry, 27(6), 1995, pp. 801-810
Three New Zealand soils of contrasting texture, organic matter content
and cation exchange capacity (CEC) were amended with K2Cr2O7 solution
s, spanning two concentration ranges, 0-5 mu mol Cr(VI) g(-1) soil and
0-50 mu mol Cr(VI) g(-1) soil. Samples were assayed for phosphatase,
sulphatase and urease enzyme activities, and for basal respiration, mi
crobial biomass C, dimethyl sulphoxide(DMSO)-reducing activity and den
itrification, 3 and 60 d after amendment. Extractability of Cr(VI) fro
m similarly amended samples was measured from 0 to 100 d. Cr(VI) prove
d to be strongly inhibiting of most of the biological properties and i
n most instances inhibition was explained by one or both of two simple
Michaelis-Menten kinetic models. The first of these (Model 1) simulat
ed fully competitive kinetics and the second (Model 2) simulated parti
ally competitive kinetics. A single inhibition constant, similar to ED
(50) as conceptualized in previous studies, could usually be calculate
d for each property in each soil. The properties could be ranked in th
e following order of decreasing sensitivity to Cr(VI): denitrification
> DMSO-reduction > sulphatase activity approximate to biomass C > pho
sphatase activity > urease activity > respiration. For the most sensit
ive property, denitrification, ED(50) values range from 63 to 730 nmol
Cr g(-1) soil. Soil mineral surface area, organic matter content and
CEC influenced the sensitivity of properties between soils. Although t
he extent of inhibition often diminished with time, the differences we
re generally much smaller than the observed decline in extractability
of Cr(VI), indicating that a persistent, long-term inhibition, outlast
ing the Cr(VI) itself, had occurred.