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November 2018
reported little mycelial growth and fewer sclerotia on rotting resi-
dues sprayed with glyphosate
8
.
Their laboratory-based research findings concluded that glypho-
sate sprays might inhibit the growth of
S. rolfsii
affecting banana
material in the field. Other herbicides such as diuron, atrazine,
simazine and metribuzin were found to have inhibitory effects on
Sclerotinia sclerotiorum
(causal organism of Sclerotinia stalk rot
in soybean) at a certain concentration tested in petri dish studies
9
.
Acetochlor treatment was shown to decrease vascular wilt due to
Fusarium oxysporum
in melon
10
.
The pre-plant application of glyphosate reportedly reduced the
incidence of red crown rot in soybean
11
, whilst reduced conidial
germination, mycelial growth and sporulation were found for
F. solani
12
(causal pathogen of sudden death syndrome). For every
study that points to a potential inhibitory effect of a fungal pathogen,
one would, however, almost always find a different article that was
unable to observe any effect at all. As already stated throughout our
series of articles, care should be taken in extrapolating what hap-
pens in the laboratory to what is observed in the field.
Some studies have indicated that glyphosate can affect growth and
reproduction in vitro, meaning where fungi or bacteria were tested
on liquid or a solid medium in a glass container, but showed adverse
effects in the field
13
– accordingly a similar situation to the glass-
house phenomenon that Powell and Swanton
6
referred to. In vitro
studies do, however, have an important role to play as far as research
goes, as they assist with establishing whether the observed effect is
due to a direct herbicide-pathogen interaction, or whether it is rather
due to an indirect effect, which results in the plant becoming less or
more resistant to the pathogen.
Two authors, Sanyal and Shrestha
7
, concluded in their article pub-
lished during 2008 titled, ‘Direct effect of herbicides on plant patho-
gen and disease development in various cropping systems’ that the
mechanisms of all possible interactions between herbicides and
plant pathogens are clearly not yet well understood. Taking
Rhizoc-
tonia solani
as an example, they state that based on what has been
published internationally, herbicides might have an important role to
play regarding managing this pathogen in crops. It was found that
R. solani
has the capability to utilise some herbicides as an energy
source
14
, whilst herbicides such as trifluralin, atrazine, paraquat and
alachlor can actually reduce
R. solani
15,16
.
They, however, continue to state that the contrasting results ob-
tained internationally suggest that the direction of interactions ob-
served between disease severity and herbicides are specific to each
crop-herbicide combination, with various other factors including
crop variety, pathogen strain, environmental conditions and adju-
vants contributing to the observed effects.
Altman and Rovira
17
probably summarised the situation best dur-
ing 1989. They concluded that it is beyond question that herbicides
affect plant diseases, but since so many factors are altered when
herbicides are used, it remains extremely challenging to identify
specific effects on a particular pathogen or host-plant relationship.
In part 4 of this series, focus will be placed on research findings
published on the impact of glyphosate and other herbicides on
earthworms. Readers are welcome to contact the
authors at ARC-Grain Crops with any enquires they
might have at 018 299 6100.
References
1
Canaday, CH, Helsel, DG and Wyllie, TD. 1986.
Effects of herbicide-induced
stress on root colonisation of soybeans by
Macrophomina phaseolina. Plant Dis.
70, 863 - 866.
2
Kremer, RJ and Means, NE. 2009.
Glyphosate and glyphosate-resistant crop in-
teractions with rhizosphere microorganisms
. Eur. J. Agron. 31, 153 - 161.
3
Fernandez, MR, Selles, F, Gehl, D, DePauw, RM and Zenthern, RP. 2005.
Crop
production factors associated with Fusarium head blight in spring wheat in east-
ern Saskatchewan
. Crop Sci. 45, 1 908 - 1 916.
4
Njiti, VN, Myers, OM, Schroeder, D and Ligthfoot, DA. 2003.
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Fusarium solani
root colonisation and sudden
death syndrome
. Agron. J. 95, 1 140 - 1 145.
5
Henriksen, B and Elen, O. 2005.
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s. J. Phyto-
pathol. 153, 214 - 220.
6
Powell, JR and Swanton, CJ. 2007.
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Fusarium
spp
. Weed Res. 48, 307 - 318.
7
Sanyal, D and Shrestha, A. 2008.
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. Weed Sci. 56, 155 - 160.
8
Westerhuis, D, Vawdrey, LL and Piper, R. 2007.
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9
Casale, WL and Hart, LP. 1986.
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10
Cohen, R, Blaier, B, Schaffer, AA and Katan, J. 1996.
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. Eur. J. Plant
Pathol. 102, 45 - 50.
11
Berner, DK, Berggren, GT and Snow, JP. 1991.
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Calonec-
tria crotolariae
and red crown rot of soybean
. Plant Dis. 75, 809 - 813.
12
Sanogo, S, Yang, XB and Scherm, H. 2000.
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Fusarium
solani f. sp.
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tolerant soybean
. Phytopath. 90, 57 - 66.
13
Burgiel, Z and Grabowski, M. 1996.
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genic and growth of
Nectria galligena Bres. Folia Hortic. 8, 13 - 19.
14
Altman, J. 1969.
Pre-disposition of sugar beets to
Rhizoctonia solani
dampling-
off with herbicides
. Phytopathol. 59, 1 015.
15
Leach, SS, Murdoch, CW and Gordon, C. 1991.
Response of selected soil-borne
fungi and bacteria to herbicides utilised in potato crop management systems in
Maine
. Am Potato J. 68, 269 - 278.
16
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cides on growth of
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17
Altman, J and Rovira, AD. 1989.
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. Can. J. Plant Pathol. 11, 166 - 172.