The mode of action of paraquat (1,1-dimethyl-4,4bipyridinium) and the mechanism of resistance to it were studied in leaves of atrazine/paraquat co-resistant (R) and susceptible (S) biotypes of horseweed {Conyza canadensis) collected from Hungarian vineyards. The application of 0-5 mol m'^ paraquat by spraying onto the surface of the leaves of intact plants in the light rapidly led to typical symptoms of paraquat action in the initial period in both biotypes, i.e. inhibition of CO2 fixation, suppression of variable chlorophyll fluorescence (Fv), decrease of oxygen evolution and stimulation of ethane production. The inhibitory effect of paraquat in the S plants was irreversible, whereas it was transient in the R plants and those plants recovered gradually afterwards. The R plants recovered from the inhibitory effect of paraquat only in the light, and an increase in light intensity was found to have a pronounced effect on the recovery of Fv. The mechanism of resistance to paraquat In C. canadensis is discussed.

Violaxanthin de-epoxidation, chlorophyll fluorescence quenching, and photosynthetic O 2 evolution in the presence of paraquat (Pq) were studied in intact attached leaves of Pq-susceptible, and Pq-resistant (PqR) biotypes of Erigeron canadensis under different light conditions. Initially, similar changes were induced in the two biotypes, but the effects relaxed only in the PqR plants, indicating a Pq elimination process. The penetration of Pq into the chloroplasts of PqR plants proved to be somewhat restricted and highly light-dependent, as revealed by both the light response curves of violaxanthin deepoxidation and fluorescence quenching and the short-term high-light pre-illumination experiments. An irregular downregulation of the non-photochemical fluorescence quenching processes was observed, reflected by lower steady-state zeaxanthin and non-photochemical fluorescence quenching levels as compared with the corresponding non-treated highlight controls. It is concluded that light is essential not only for the initiation of the mechanism of resistance to Pq, but also for the penetration of Pq into the chloroplasts in the PqR E. canadensis. Also, the Pq elimination process may cause a modification to the regulation of the non-radiative energy dissipation in PqR plants in the presence of Pq.

The Ser264ÆGly substitution on the D1 protein is accompanied by a higher photosensitivity of the mutant plant. This may be due to an increased D1 protein turnover and/or to a lower xanthophyll cycle activity in vivo. The relative importance of these two photoprotective mechanisms in wild and D1 protein mutant biotypes of Erigeron canadensis L. was established by using dithiothreitol and streptomycin. Moreover, the interconversion of violaxan-thin to zeaxanthin via antheraxanthin was studied in isolated thylakoids and in intact leaves treated with paraquat. Streptomycin caused a more severe decrease in the optimal quantum yield (Fv/Fm) of PS II and a large increase in the initial fluorescence yield (Fo) in the mutant compared to the wild biotype. In the fluorescence-quenching parameters of the wild-type leaves, dithiothreitol caused alterations similar to those observed in the mutant plant without dithiothreitol. A lowered activity of the xanthophyll cycle was detected in the mutant biotype compared to the wild-type in vivo. However, under in vitro, conditions which were optimal for violaxanthin de-epoxidation, or when paraquat was used on intact leaves to accelerate the electron transport, violaxanthin could readily be converted to zeaxanthin even in the mutant plants. This demonstrates that neither the decrease in the enzymatic activity of violaxanthin de-epoxidase nor the low availability of violaxanthin is responsible for the low zeaxanthin formation under in vivo conditions. It is presumed that, in vivo, the D1 protein mutation results in slower electron transport, a smaller DpH and lower zeaxanthin formation, and thereby in alterations in the defensive strategies against high light illumination.

Insensitivity to atrazine [2-chloro-4-(ethylamino)-6-(isopropylamino)-s-triazine] and certain other herbicides was found in plants of horseweed (Conyza canadensis(L.) Crong. ♯4ERICA) collected from vineyards where atrazine had been applied extensively. There were no differences in the uptake, translocation, or accumulation of radiolabeled atrazine between plants of the susceptible and resistant biotypes. However, atrazine at 1 × 10-4M caused no inhibition of photosynthetic electron transport in resistant leaves. Photosynthetic characteristics of leaves of susceptible and resistant plants showed different sensitivities to atrazine, but similar sensitivities to diuron [3-(3,4-dichlorophenyl)-1,1-dimethylurea] and ioxynil (4-hydroxy-3,5-diiodobenzonitrile). Isolated chloroplast membranes from resistant plants exhibited a resistance factor of 1000 to atrazine but only 10 to 30 to methylthio-s-triazines. DNOC (4,6-dinitro-o-cresol) was found to be more effective in susceptible chloroplasts than in resistant ones. A marked reduction in the galactolipid content, especially digalactosyl diglyceride, was found in resistant leaves. It is suggested that these alterations in lipid content and composition may contribute to atrazine resistance in horseweed.

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