Echinochloa oryzoides and E. phyllopogon have become the most serious weeds in California Oryza sativa since continuous flooding was used to suppress E. crus-galli. Continuous use of a limited number of available graminicides and an increasing number of control failures led to the investigation of herbicide resistance in E. oryzoides and E. phyllopogon. Greenhouse dose-response studies with postemergence (POST) applications of molinate, thiobencarb, fenoxaprop-ethyl, and bispyribac-sodium estimating GR50 (herbicide dose to inhibit growth by 50%) values suggested resistance to all herbicides in two E. phyllopogon accessions and to molinate and thiobencarb in one E. oryzoides accession when compared with susceptible E. phyllopogon and E. oryzoides controls, respectively. No resistance was detected in dose-response studies with propanil. Minimum and maximum ratios (R/S) of the GR50 values of resistant to susceptible E. phyllopogon plants (in two experiments involving two resistant accessions) were 7.8 and >13.3 for thiobencarb, 2.2 and 4.3 for molinate, 16.5 and 428.7 for fenoxaprop-ethyl, and 2.0 and 12.0 for bispyribac-sodium. Minimum and maximum E. oryzoides R/S ratios (average of two experiments) were 21.9 and 4.6 for thiobencarb and molinate, respectively. A resistant E. phyllopogon (one accession tested) and the susceptible control were killed by POST applications of glyphosate, glufosinate, and clomazone, and by a preemergence application of pendimethalin. Thus, the repeated use of the few available grass herbicides in the predominantly monocultured O. sativa of California has selected for herbicide resistance in E. oryzoides and E. phyllopogon. The introduction of herbicides with new mechanisms of action will be useful to manage herbicide-resistant E. oryzoides and E. phyllopogon. However, cross- and multiple resistance emphasize the need to integrate herbicide use with nonchemical means of weed management.
Paclobutrazol [(2RS,3RS)-1-(4-chlorophenyl)methyl-4,4-dimethyl-2-(1h-1,2,4-trizol-1-yl)penten-3-ol] effectively decreased vegetative growth of rice (Oryza sativa L.) seedlings and increased the chlorophyll content. The number of veins in a leaf, the calculated number of stomata per leaf, and the length of guard cells were not altered by the paclobutrazol treatment, suggesting an effect on cell elongation. The allocation pattern of carbohydrates was changed by either gibberellin (GA) or paclobutrazol treatment. GA 3 induced more shoot growth and less accumulation of starch than the control and paclobutrazol-treated seedlings. Photosynthetic ability was not affected by either paclobutrazol or GA 3 treatment. Paclobutrazol-treated plants allocated a smaller amount of photosynthates for vegetative shoot growth and stored more as starch in the crowns than the control and GA 3 -treated plants. The same starch degrading activity in the crown tissue of paclobutrazol-treated seedlings as in control plants suggests that the accumulated starch is utilized in a normal activity for growth including leaf emergence, tiller formation, and root production, resulting in improved seedling quality.
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