2013
DOI: 10.1002/ps.3447
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Ecotoxicological characterisation of a mycoherbicide mixture isolated from the fungus Ascochyta caulina

Abstract: The present study has provided baseline information needed to assess the potential hazard of the fungal toxins of A. caulina. In particular, the acute and chronic effects on aquatic (algae, Daphnia and fish) and terrestrial organisms (earthworms) have been highlighted. Finally, a comparison of the inherent toxicity of ACTs with other synthetic herbicides has shown comparative ecotoxicity of the tested mixture.

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Cited by 14 publications
(11 citation statements)
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References 23 publications
(29 reference statements)
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“…Many fungi are known to produce very toxic compounds such as mycotoxins constraining the use of some effective but toxigenic mycoherbicidal agents (e.g., based on Fusarium spp.). Moreover, despite a number of registered mycoherbicides and a long list of potential ones [7], the toxicological risks of their application have been evaluated on limited number of fungal species such as Stagonospora convolvuli, Ascochyta caulina, Myrothetium verrucarium [8][9][10]. Recently, among phytotoxic compounds isolated from S. cirsii, a potential bioherbicide for Sonchus arvensis biocontrol, the most potent stagonolide A was considered as a mycotoxin due to a broad spectrum of biological activity [11,12].…”
Section: Introductionmentioning
confidence: 99%
“…Many fungi are known to produce very toxic compounds such as mycotoxins constraining the use of some effective but toxigenic mycoherbicidal agents (e.g., based on Fusarium spp.). Moreover, despite a number of registered mycoherbicides and a long list of potential ones [7], the toxicological risks of their application have been evaluated on limited number of fungal species such as Stagonospora convolvuli, Ascochyta caulina, Myrothetium verrucarium [8][9][10]. Recently, among phytotoxic compounds isolated from S. cirsii, a potential bioherbicide for Sonchus arvensis biocontrol, the most potent stagonolide A was considered as a mycotoxin due to a broad spectrum of biological activity [11,12].…”
Section: Introductionmentioning
confidence: 99%
“…1, Table S1 ESI †), was isolated from the mixture of toxins obtained by a basic eluate of cation exchange chromatography carried out on the fungal culture ltrates. 39 A new phytotoxic enol tautomer of 4-pyridylpyruvic acid, named ascosonchine (4, Fig. Furthermore, the simultaneous application of toxins or fungal spores, together with low doses of synthetic herbicides (metribuzin and rimsulfuron at 1/5 of the labeled rate), gave better results than single-agent treatments.…”
Section: Introductionmentioning
confidence: 99%
“…The results obtained in both acute and chronic toxicity tests with Eisenia foetida indicated a very low toxicity of ACTs for terrestrial organisms. In general, the comparison of the ecotoxicological profile of ATCs with other herbicides has shown a lower ecotoxicity for the tested mixture [24].…”
Section: Ecotoxicological Characterization Of a Mycoherbicide A Caulmentioning
confidence: 87%