Microbial volatilization of selenium as dimethylselenide (DMSe) and dimethy
ldiselenide (DMDSe) from soil is an important part of the Se cycle in natur
e, but little is known about the stability and transformations of these gas
es during residence in the soil environment before dissipation to the atmos
phere. Experiments monitored by gas chromatography and atomic absorption sp
ectroscopy were made with various clay mineral standards, charcoal, commerc
ial humic substances and soils to determine the sorption and transformation
s of DMSe and DMDSe injected into the headspace or passed through soil mate
rials. Batch experiments conducted with 2-5 g materials placed into 40 mL T
eflon centrifuge tubes equipped with Mininert(R) gas sampling valves showed
that DMSe was slowly sorbed by soil materials and most of the DMSe deficit
in the headspace was recovered as SeO3= and Se-4(=). In contrast, DMDSe wa
s rapidly partitioned from the gas phase and resulted in an increased recov
ery of less soluble elemental and selenide-Se forms. These results were con
firmed during flow-through soil column studies with both little DMSe sorpti
on and sorption of the majority of DMDSe addition. Additions of selenomethi
onine (SeMet) to soil to produce DMSe and DMDSe in sealed flasks resulted i
n an increased partitioning of Se into inorganic Se when compared with a fl
ow-through system designed to limit the contact of Se gases with soil. Thes
e results suggest that soil Se volatilization as DMSe and DMDSe results in
Se loss to the atmosphere as DMSe with concomitant soil Se immobilization d
ue to the instability of DMDSe. (C) 1999 Elsevier Science Ltd. All rights r
eserved.