Target Sites for Herbicide Action 1991
DOI: 10.1007/978-1-4899-2433-9_1
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Photosynthesis

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Cited by 6 publications
(3 citation statements)
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“…Photosynthetic inhibitors, such as the Photosystem II (PS II) electron transport inhibitor diuron (review by Dodge17), effectively inhibited the Hill reaction using isolated thylakoids from wheat with ferricyanide as electron acceptor (Fig 1). This light‐dependent in vitro activity correlated with in vivo effects, including inhibition of phototrophic growth in algae and Lemna and reduced carbon assimilation of Galium plants.…”
Section: Resultsmentioning
confidence: 99%
“…Photosynthetic inhibitors, such as the Photosystem II (PS II) electron transport inhibitor diuron (review by Dodge17), effectively inhibited the Hill reaction using isolated thylakoids from wheat with ferricyanide as electron acceptor (Fig 1). This light‐dependent in vitro activity correlated with in vivo effects, including inhibition of phototrophic growth in algae and Lemna and reduced carbon assimilation of Galium plants.…”
Section: Resultsmentioning
confidence: 99%
“…Resistance has been assumed to be associated with alterations to physiologic and/or morphologic traits in the phenotypes that inhibit herbicide uptake, translocation, site of action, or metabolism [29]. In all but a few plant biotypes resistant to photosystem II inhibitors (primarily the s-triazines), their resistance is due to a modification of amino acid residues on the D-1 pigment protein at the target site [30,31]. This may not account for resistance of S. alterniflora for growth inhibition measured at 1 week is consistent for plants with a met-abolic basis for tolerance.…”
Section: Discussionmentioning
confidence: 99%
“…Resistance has been assumed to be associated with alterations to physiologic and/or morphologic traits in the phenotypes that inhibit herbicide uptake, translocation, site of action, or metabolism [29]. In all but a few plant biotypes resistant to photosystem II inhibitors (primarily the s ‐triazines), their resistance is due to a modification of amino acid residues on the D‐1 pigment protein at the target site [30,31]. This may not account for resistance of S. alterniflora for growth inhibition measured at 1 week is consistent for plants with a metabolic basis for tolerance.…”
Section: Discussionmentioning
confidence: 99%