An apparatus was developed for the rapid and facile evaluation of soil fumi
gants in a controlled manner using small volumes of soil, The apparatus con
sisted of a manifold to which were attached six canisters containing a loam
y sand soil (adjusted to -100 kPa soil water potential). The soil was infes
ted with either conidia of Fusarium oxysporum or Trichoderma harzianum; scl
erotia of Sclerotinia minor; ascospores of Talaromyces flavus; vermiculite
colonized with Pythium aphanidermatum; or beet (Beta vulgaris L., cv, Detro
it Red) seed colonized with Rhizoctonia solani, Using nitrogen gas (N-2) as
a carrier gas, either N-2 or N(2)plus benzaldehyde was passed continuously
through the soil for 24, 48, or 72 hours. At all three exposure times, ben
zaldehyde + N-2 reduced viability of R. solani and S. minor, and reduced po
pulations of P. aphanidermatum and T. harzianum. Populations of F. oxysporu
m were reduced after 48 and 72 hours of exposure to benzaldehyde, whereas p
opulations of T. flavus were reduced only after 72 hours of exposure. Fumig
ation with benzaldehyde + N-2 for 24 hours did not affect soil pH 1 week af
ter exposure, but fumigation for 48 or 72 hours temporarily lowered pH from
an average of 6.86 to 5.57 and 5.32, respectively. The biocontrol fungus,
T. flavus, was less sensitive to benzaldehyde than the pathogens or the bio
control fungus, T. harzianum, Thus, combining T. flavus with benzaldehyde t
o enhance biocontrol may be possible.