Smallflower umbrella sedge is a prolific C3 weed commonly found in rice fields in 47 countries. The increasing infestation of herbicide-resistant smallflower umbrella sedge populations threatens rice production. Our objectives for this study were to characterize thermal requirements for germination of smallflower umbrella sedge seeds from rice fields in California and to parameterize a population thermal-time model for smallflower umbrella sedge germination. Because the use of modeling techniques is hampered by the lack of thermal-time model parameters for smallflower umbrella sedge seed germination, trials were carried out by placing field-collected seeds in a thermogradient table set at constant temperatures of 11.7 to 41.7 C. Germination was assessed daily for 30 d, and the whole experiment was repeated a month later. Using probit regression analysis, thermal time to median germination [θT(50)], base temperature for germination (Tb), and SD of thermal times for germination [σθT(50)] were estimated from germination data, and model parameters were derived using the Solver tool in Microsoft Excel®. Germination rates increased linearly below the estimated optimum temperatures of 33.5 to 36 C. Estimated Tb averaged 16.7 C, whereas θT(50) equaled 17.1 degree-days and σθT(50) was only 0.1 degree-day. The estimated Tb for smallflower umbrella sedge is remarkably higher than that of japonica and indica types of rice, as well as Tb of important weeds in the Echinochloa complex. Relative to the latter, smallflower umbrella sedge has lower thermal-time requirements to germination and greater germination synchronicity. However, it would also initiate germination much later because of its higher Tb, given low soil temperatures early in the rice growing season in California. When integrated into weed growth models, these results might help optimize the timing and efficacy of smallflower umbrella sedge control measures.
Determining the mechanisms of herbicide resistance in weeds allows for the development and implementation of applied management practices aimed to control and to prevent further spread of herbicide-resistant populations in crop fields. This research was conducted to determine propanil resistance and cross-resistance to other photosystem II (PSII) inhibitors in ricefield bulrush biotypes and to elucidate the mechanism of propanil resistance. To this end, propanil-resistant (R) and propanil-susceptible (S) biotypes were selected from field-collected populations after propanil spraying at the field rate, and whole-plant, dose–response experiments were conducted to evaluate cross-resistance to PSII inhibitors and interactions between propanil and the insecticides malathion and carbaryl. In addition, thepsbAgene from R and S biotypes was sequenced for amino acid alterations following polymerase chain reaction (PCR) amplification. Plant survival data indicated the R biotype displayed a 14-fold increase in propanil resistance relative to the susceptible (S) biotype. In addition, the propanil-R biotype also had increased resistance to the PSII-inhibitors bromoxynil, diuron, and metribuzin but was more susceptible to bentazon than were propanil-S plants. Synergism between propanil and the insecticides carbaryl and malathion was greater in the S biotype than it was in the R biotype, indicating that, unlike propanil resistance in weedy grasses, enhanced degradation of the herbicide molecule is not a mechanism of resistance for propanil in ricefield bulrush. A Val219to Ile substitution in the propanil-R chloroplast D1 protein was identified following sequencing of thepsbAgene. This research suggests a single-point mutation at the target site causes resistance to propanil, diuron, metribuzin, and bromoxynil but increasing susceptibility to bentazon in propanil-R ricefield bulrush, a novel Val219–Ile feature. To our knowledge, this is the first instance of propanil resistance in weeds because of a mechanism other than enhanced herbicide metabolism. Tank-mixing bentazon and propanil, where permitted, can control both propanil-R and propanil-S biotypes.
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