Abstract:
“Biofumigation” is an alternative method to chemical fumigants for controling soil borne
pathogens and pests. The term is specifically used to describe the utilization of naturally
occurring biotoxic isothiocyanates (ITC) that evolve as hydrolysis products from glucosinolate
(GSL)-containing plants or plant products applied to soil. In Mediterranean countries, Brassica
species are particularly important vegetables since they are major winter crops and are
considered to be rich sources of health promoting substances. After harvesting, the plant
residues may be incorporated into the soil. The “biofumigation” potential of these residues
depends on various factors that affect the toxicity of the GSL hydrolysis products to soil
microorganisms, such as the size of biomass incorporation, the GSL concentration and type and
the environmental conditions, .
GSL content and profile in Brassica species are influenced by plant factors, such as
species and developmental stage, as well as by environmental conditions. The later include
nutrient availability, especially nitrogen (N) and sulfur (S) supply. Sulfur is a key element for the
GSL biosynthetic pathway, since it is assimilated by plants into organic sulfur-rich molecules as
methionine and cysteine which are precursor molecules of GSLs. N is an essential element highly
related with plant growth, protein-synthesis and agricultural production; moreover it is co-related
with S in several biosynthetic processes within plant including GSL biosynthesis.
The aims of this study was (1) to investigate the effects of S and N fertilization on the
distribution of different GSL in different plant organs of Brassica species and varieties with
emphasis to the plants broccoli (Brasica oeracea var. italica) and rocket (Eruca sativa) and (2) to
examne the effects of the GSLs to the soil microbial community when they are introduced into the
soil with the incorporation of the respective plant residues.
The extend of S assimilation in GSL as a percentage of total plant-S was examined in
Chapter 3. Moreover, different N and S fertilization doses were applied in order to examine the
response of GSL concentration in two different Brassica species, broccoli (Brassica oleraceae var.
Italica) and rocket (Eruca sativa M.). In addition a relationship between N-NO3
- and biomass
production in terms of critical levels was established in both species in order to optimize N use
(Chapter 4 and 5). The impact of the incorporation of broccoli residues as a “biofumigant” on the
soil microbial community and activity was investigated in comparison with chemical fumigation
(Chapter 6); whereas a more detail examination of ascomycetes and ammonia oxidizers
community structure using molecular techniques was examined in Chapter 7. Finally, GSL
dissipation in soils under two different %WHC regimes was examined using pure GSL and
broccoli plant residues (Chapter 8).
The results of the current study clearly showed that GSL profile and concentration
depends on Brassica species, variety and plant organ. Moreover N and S supply rate had a
significant impact on GSL concentration found in broccoli and rocket tissues. It was evident that N influenced the individual GSL profile in the various organs that were examined in both species
whereas S had a pronounced effect on their concentration. Furthermore, besides N and S
fertilization, plant developmental stage had a detrimental effect on GSL concentration. Therefore
it was concluded that GSL profile and content of the plant organs, of these species could be
optimized and regulated (increased) using appropriate fertilization schemes and harvesting times.
However it was showed that the response of different Brassica species in N and S fertilization
differs, therefore, specific research is needed for other species in order to optimize their GSL
content through fertilization.
Incorporation of broccoli residues in soil didn’t reduced microbial activity in comparison
with conventional soil fumigation practices such as fumigation with metham sodium. Instead an
increase of soil microbial activity was noticed. The differences that were observed after broccoli
residues incorporation in the soil are not associated with the GSL content of the residues and
their subsequent hydrolysis products (ITC). It seems that the impact of broccoli residues on the
soil microbial activity and community is related with their general role in soils as carbon sources.
The persistence of GSL in soil is very short and the increase of soil water content is
negatively related with their persistence in the medium. This was noticed when they were applied
either as pure substances or through incorporation of broccoli residues. Dissipation of pure GSL
in soils seems to be related with microbial myrosinase activity or other GSL degradating enzymes
(probably sulfatases); whereas plant derived GSL dissipation is more related with plantmyrosinase
activity.
In conclusion, this work indicates that the suppressive impact of broccoli residues to
various soil borne pathogens, which is mentioned in literature, is not related with their GSL
content. Incorporation of plant residues belonging to a different species than broccoli, with higher
GSL content, could be more effective and this effect could perhaps be attributed in GSL content.
Under these circumstances, optimization of plant GSL content through fertilization with N and S
could be accomplished. Higher “biofumigation” potential could be also increased by incorporation
of plant material at the appropriate developmental stage and by optimization of abiotic factors
during incorporation that are involved in GSL hydrolysis and ITC production such as soil water
content.
High GSL containing pre-selected plant species, incorporated under high soil water
conditions, could be combined with other alternative techniques such as soil solarization for the
control of soil borne pathogens and pests. These issues will be the target of future research
activities for the development, optimization and evaluation of sustainable agricultural practices.