Biological denitrification is the microbial dissimilative reduction of
nitrates or nitrites to produce gaseous nitrous oxide arid elemental
nitrogen. As reported by some authors (T i e d j e et al., 1984), the
ability to denitrify is a property very much spread among soil microor
ganisms. For this reason and for the general importance of denitrifica
tion in the soil nitrogen cycle, denitrification activity (or any othe
r characteristics of denitrification) can be considered as an importan
t soil biological parameter. The present contribution summarizes the p
rinciples of the determination of denitrification. Two methods of meas
uring denitrification activity are described in detail: the method of
inhibition of N2O reduction by acetylene (acetylene inhibition method)
and the method of reduction of added N2O. Results of denitrification
measurement by the acetylene inhibition method in soil cores, taken fr
om three stages of a secondary succession on entric cambisol, are pres
ented. It follows from the results given in Tab. I, that there is a ma
rked seasonal variability of denitrification activity - the highest va
lues were recorded in spring. A high general variability of the result
s, expressed by variation coefficients, is also evident. This denitrif
ication activity represents a certain actual soil parameter which is s
trongly influenced by environmental factors and characterized by consi
derably high space heterogeneity. Furthermore, results of denitrificat
ion activity measurement in soil layers of mollisol in samples in the
form of sieved and homogenized soil, incubated under partly optimized
conditions (preincubation, glucose addition), are presented. Denitrifi
cation was measured simultaneously using two different techniques: ace
tylene inhibition method and method of the reduction of N2O added. Bot
h methods gave similar results (Tab. II). The highest denitrification
activity was found in the surface layer 0 to 4 cm, and it decreased wi
th the depth. A significantly lower variability of the results is appa
rent in comparison with the results presented in Tab. I. Data on the d
enitrification activity measured under optimum conditions reflect die
suitability or unsuitability of various environmental and soil conditi
ons for denitrifiers and denitrification on the site prior to sampling
. It was concluded that the measurement of denitrification enzyme acti
vity - the DEA method (T i e d j e et al., 1989) should be a suitable
method for quantification of denitrification as a microbial soil param
eter. Using this method all three most important conditions of denitri
fication are optimized: pO2, nitrate and carbon. This possibility is t
o be verified.