Relationship between safening activity of dymron and fenclorim to pretilachlor and glutathione S-transferase activity in rice

Dymron [1‐(α,α‐dimethybenzyl)‐3‐(p‐tolyl)urea] and fenclorim (4,6‐dichloro‐2‐phenylpyrimidine) were found to exhibit a safening activity on the growth of rice (Oryza sativa L.) seedlings against pretilachlor [2‐chloro‐2′,6′diethyl‐N‐(2‐propoxyethyl)acetanilide] injury. By pretilachlor treatment at 10^–6 and 10^–5 mol L^–1, the elongation of the third leaves of rice seedlings was reduced by approximately 20 and 40%, and that of the fourth leaves was reduced by approximately 40 and 80%, respectively. Upon the treatment of dymron at 3 × 10^–6 and 10^–5 mol L^–1 in combination with pretilachlor, the growth inhibition was half alleviated in the third leaves, and the length of the fourth leaves was almost recovered from 10^–6 mol L^‐1 pretilachlor injury, and was 20–25% recovered from 10^–5 mol L^–1 pretilachlor injury. Upon the treatment of fenclorim at 3 × 10^–6 and 10^–5 mol L^–1 in combination with pretilachlor, the growth inhibition of rice seedlings was almost alleviated in both the third and the fourth leaves. This result indicated that dymron and fenclorim showed almost the same safening effect on the fourth leaf growth against 10^–6 mol L^‐1 pretilachlor injury, although fenclorim showed higher effects at higher concentrations of pretilachlor. Glutathione S‐transferase (GST) activities in rice seedlings were investigated after being treated with a herbicide and safener. By pretilachlor treatment at 10^–6 and 10^–5 mol L^–1, the GST activity was approximately 32 and 72% increased in roots, respectively, and a little increased (7–13%) in shoots of two‐leaf‐stage rice seedlings. By dymron treatment at 3 × 10^–6?10^–5 mol L^–1, the GST activity was 2–30% increased in roots, but was not increased in shoots. By their combination treatment, the GST activity was almost the same or less than that by treatment with pretilachlor alone. In contrast, by fenclorim treatment alone, the GST activity was 43–52 and 33–45% increased in roots and shoots of rice seedlings, respectively. By the combination treatment of pretilachlor and fenclorim, the GST activity was increased 73–126% in shoots and 101–139% in roots, and was much more increased in both shoots and roots compared with treatment of pretilachlor or fenclorim alone. It was found that dymron showed less effect in increasing the GST activity than fenclorim. It is also suggested that dymron did not increase the GST activity in shoots but did increase it slightly in roots, and showed almost no effect on GST increase by pretilachlor in shoots, or rather reduced the increase in roots. From the above results, fenclorim and dymron may have different mechanisms of safening effects on the protection of rice seedlings against pretilachlor injury.     

Testing a chemical series inspired by plant stress oxylipin signalling agents for herbicide safening activity

BACKGROUND

Herbicide safening in cereals is linked to a rapid xenobiotic response (XR), involving the induction of glutathione transferases (GSTs). The XR is also invoked by oxidized fatty acids (oxylipins) released during plant stress, suggesting a link between these signalling agents and safening. To examine this relationship, a series of compounds modelled on the oxylipins 12‐oxophytodienoic acid and phytoprostane 1, varying in lipophilicity and electrophilicity, were synthesized. Compounds were then tested for their ability to invoke the XR in Arabidopsis and protect rice seedlings exposed to the herbicide pretilachlor, as compared with the safener fenclorim.

RESULTS

Of the 21 compounds tested, three invoked the rapid GST induction associated with fenclorim. All compounds possessed two electrophilic carbon centres and a lipophilic group characteristic of both oxylipins and fenclorim. Minor effects observed in protecting rice seedlings from herbicide damage positively correlated with the XR, but did not provide functional safening.

CONCLUSION

The design of safeners based on the characteristics of oxylipins proved successful in deriving compounds that invoke a rapid XR in Arabidopsis but not in providing classical safening in a cereal. The results further support a link between safener and oxylipin signalling, but also highlight species‐dependent differences in the responses to these compounds. © 2018 The Authors. Pest Management Science published by John Wiley & Sons Ltd on behalf of Society of Chemical Industry.     

Differential safening activity of dymron and fenclorim on pretilachlor injury in rice seedlings in soil

The safening activity of dymron [1-(α,α-dimethylbenzyl)-3-( p -tolyl)urea] and fenclorim [4,6-dichloro-2-phenylpyrimidine] on the phytotoxic activity of pretilachlor [2-chloro-2',6'-diethyl- N- (2-propoxyethyl)acetanilide] on rice seedlings was examined in both water and soil culture. The safening activity of fenclorim in water culture was greater than that of dymron, whereas the activity of fenclorim in soil was lower than that of dymron. The fenclorim concentration in soil water was lower than that of dymron at all times when determined after the application at the same concentrations. The phytotoxic activity of pretilachlor and the safening activities of dymron and fenclorim were well correlated with the concentration of each in soil water but not with the amount in total soil. The adsorption of fenclorim on soil solids was greater than those of dymron and pretilachlor. It was suggested that both the phytotoxic activity of pretilachlor and the safening activities of dymron and fenclorim were dependent on their concentrations in soil water, which were primarily dominated by the adsorption on soil.     

Translocation and degradation of pyrazosulfuron-ethyl in rice soil

BACKGROUND: Pyrazosulfuron‐ethyl {ethyl 5‐[(4,6‐dimethoxypyrimidin‐2‐ylcarbamoyl)‐sulfamoyl]‐1‐methylpyrazole‐4‐carboxylate} is a new rice herbicide belonging to the sulfonylurea group. This study reports the translocation of ¹⁴C‐pyrazosulfuron‐ethyl to rice plants and its degradation in rice‐planted and unplanted soil. RESULTS: Pyrazosulfuron‐ethyl did not show any appreciable translocation to rice shoots, as ¹⁴C‐activity translocated to the aerial portion never exceeded 1% of the initially applied ¹⁴C‐activity over a 25 day period. Results suggested that the dissipation of pyrazosulfuron‐ethyl from soils followed first‐order kinetics with a half‐life of 5.5 and 6.9 days in rice‐planted and unplanted soils respectively. HPLC analysis of the organic extract of soil samples showed the formation of three metabolites, namely ethyl 5‐(aminosulfonyl)‐1‐methyl‐1‐H‐pyrazole‐4‐carboxylate, 5‐[({[(4,6‐dimethoxy‐2 pyrimidinyl)‐amino]‐carbonyl} amino)‐sulfonyl]‐1‐methyl‐1H‐pyrazole‐4‐carboxylic acid and 2‐amino‐4,6‐dimethoxy pyrimidine, in both rice‐planted and unplanted soils. CONCLUSION: The study indicates that pyrazosulfuron‐ethyl was a short‐lived compound in the soil and was degraded relatively faster in rice‐planted soil than in unplanted soil. The herbicide did not show any appreciable translocation to rice plants. Copyright © 2011 Society of Chemical Industry     

Herbicide safeners: a review

Herbicide safeners selectively protect crop plants from herbicide damage without reducing activity in target weed species. This paper provides an outline of the discovery and uses of these compounds, before reviewing literature devoted to defining the biochemical and physiological mechanisms involved in safener activity. Emphasis is placed on the effects of safeners on herbicide metabolism and their interactions with enzyme systems, such as cytochrome P₄₅₀ mono-oxygenases and glutathione-S-transferases. Attention is drawn to the potential wide-ranging applications of safeners and, in particular, their use as powerful research tools with which to identify and manipulate those mechanisms which contribute to herbicide selectivity and resistance. © 1999 Society of Chemical Industry     

除草剂安全剂对作物细胞色素P450及其他酶活性和水平的影响

综述了除草剂安全剂对作物中参与除草剂解毒作用的酶以及作为除草剂作用靶标位点酶水平与活性的影响。安全剂能增强细胞色素P450酶系统活性,诱导P450在除草剂降解中的作用;增加作物体内谷胱甘肽的含量,从而促进除草剂与谷胱甘肽的轭合而发挥解毒作用;降低由于除草剂对乙酰乳酸合成酶的抑制作用而引起的植物毒性等。     

The basis for the safening of clomazone by phorate insecticide in cotton and inhibitors of cytochrome P450s

Clomazone may be safely used in cotton to manage weeds when applied following treatments of the organophosphate insecticides phorate or disulfoton. The loss of chlorophyll and carotenoids with 6 days of 100 nM clomazone treatment of cotton seedlings was partially prevented with phorate in hydroponic solution in a rate-dependent manner. In a study to examine the timing of safening from a one-day clomazone (100 nM) treatment, maximum safening was achieved when phorate (50 μM) was applied the same day as clomazone. Phorate decreased metabolism of ¹⁴C-clomazone to polar metabolites in excised cotton shoots and shoots of intact cotton plants. Microsomal studies of corn shoots showed an NADPH-dependent/cytochrome P450 reaction was inhibited by phorate. Additional studies with corn microsomes, corn seedlings and cotton seedlings supported the basis of clomazone safening is the inhibition of toxic clomazone metabolism by P450 inhibitors.     

Spontaneous ultraweak photon emission from rice (Oryza sativa L.) and paddy weeds treated with a sulfonylurea herbicide

All living organisms spontaneously generate ultraweak photon emissions, which originate from biochemical reactions in cells. Current research uses the ultraweak photon emissions from organisms as a novel tool to investigate the physiological states of plants. In this study, we found ultraweak photon emissions from leaf segments of rice and several paddy weed species treated with a sulfonylurea herbicide. There is a definite difference in photon emissions among plant species, and rice (Oryza sativa), barnyardgrass (Echinochloa crus-galli) and Cyperus serotinus showed extremely strong enhancement of photon emissions. Photon emissions from these three species treated with sulfonylurea herbicide were suppressed when the leaf segments were treated with the cytochrome P450 monooxygenase (P450) inhibitors, piperonyl butoxide and malathion. These results suggest that P450 inhibitors affect the ultraweak photon emissions from plants.     

The interactions between piperonyl butoxide and E4, a resistance‐associated esterase from the peach‐potato aphid,Myzus persicae Sulzer (Hemiptera: Aphididae)

BACKGROUND: It has been reported previously that piperonyl butoxide (PBO) can inhibit both P450 and esterase activity. Although the method by which PBO combines with cytochrome P450 has been identified, the way in which it acts as an esterase inhibitor has not been established. This paper characterises the interactions between PBO and the resistance‐associated esterase in Myzus persicae, E4. RESULTS: After incubation with PBO/analogues, hydrolysis of 1‐naphthyl acetate by E4 is increased, but sequestration of azamethiphos is reduced. Rudimentary in silico modelling suggests PBO docks at the lip of the aromatic gorge. CONCLUSIONS: PBO binds with E4 to accelerate small substrates to the active‐site triad, while acting as a blockade to larger, insecticidal molecules. Structure–activity studies with analogues of PBO also reveal the essential chemical moieties present in the molecule. © 2012 Society of Chemical Industry     

Persistence of pyrazosulfuron in rice-field and laboratory soil under Indian tropical conditions

BACKGROUND: Pyrazosulfuron ethyl, a new rice herbicide belonging to the sulfonylurea group, has recently been registered in India for weed control in rice crops. Many field experiments revealed the bioefficacy of this herbicide; however, no information is available on the persistence of this herbicide in paddy soil under Indian tropical conditions. Therefore, a field experiment was undertaken to investigate the fate of pyrazosulfuron ethyl in soil and water of rice fields. Persistence studies were also carried out under laboratory conditions in sterile and non‐sterile soil to evaluate the microbial contribution to degradation. RESULTS: High‐performance liquid chromatography (HPLC) of pyrazosulfuron ethyl gave a single sharp peak at 3.41 min. The instrument detection limit (IDL) for pyrazosulfuron ethyl by HPLC was 0.1 µg mL^?1, with a sensitivity of 2 ng. The estimated method detection limit (EMDL) was 0.001 µg mL^?1 and 0.002 µg g^?1 for water and soil respectively. Two applications at an interval of 10 days gave good weed control. The herbicide residues dissipated faster in water than in soil. In the present study, with a field‐soil pH of 8.2 and an organic matter content of 0.5%, the pyrazosulfuron ethyl residues dissipated with a half‐life of 5.4 and 0.9 days in soil and water respectively. Dissipation followed first‐order kinetics. Under laboratory conditions, degradation of pyrazosulfuron ethyl was faster in non‐sterile soil (t_1/2 = 9.7 days) than in sterile soil (t_1/2 = 16.9 days). CONCLUSION: Pyrazosulfuron ethyl is a short‐lived molecule, and it dissipated rapidly in field soil and water. The faster degradation of pyrazosulfuron in non‐sterile soil than in sterile soil indicated microbial degradation of this herbicide. Copyright © 2012 Society of Chemical Industry     

Inheritance of resistance to fenoxaprop‐p‐ethyl in sprangletop (Leptochloa chinensis L. Nees)

Sprangletop (Leptochloa chinensis L. Nees) is a serious grass weed in direct‐seeded rice cropping systems in Thailand. One population of sprangletop, BLC1, was found to be resistant to fenoxaprop‐p‐ethyl at 62‐fold the concentration of a susceptible biotype, SLC1. This study elucidated the inheritance of resistance to fenoxaprop‐p‐ethyl in this sprangletop BLC1 genotype. The reaction to the herbicide at 0.12–2.4 mg ai L^?1 was determined in the seedlings of self‐pollinated resistant BLC1, susceptible SLC1 and SLC1 that had been allowed to cross‐pollinate with BLC1. At 0.24 mg ai L^?1, all the seedlings of SLC1 were killed, while 99% of BLC1 survived, along with 5% of the cross‐pollinated SLC1 seedlings, which were considered to be putative F₁ hybrids. The root and shoot lengths of the F₁ hybrids in 0.24 mg ai L^?1 of fenoxaprop‐p‐ethyl, relative to those in the absence of the herbicide, were close to or the same as the resistant parent, indicating that the resistance is a nearly complete to complete dominant trait. One‐hundred‐and‐forty‐one of the F₂‐derived F₃ families were classified by their response to the herbicide at 0.24 and 0.48 mg ai L^?1 into 39 homozygous susceptible : 72 segregating : 30 homozygous resistant, fitted with a 1:2:1 ratio at χ² = 1.21 and P = 0.56, indicating that the resistance to fenoxaprop‐p‐ethyl in the sprangletop BLC1 genotype is controlled by a single gene.     

Isolation and functional characterization in yeast of CYP72A18, a rice cytochrome P450 that catalyzes (ω-1)-hydroxylation of the herbicide pelargonic acid

Cytochrome P450 proteins play important roles in plant herbicide selectivity. Here, we demonstrate metabolism of the herbicide pelargonic acid by CYP72A18, a novel cytochrome P450 isolated from the rice Oryza sativa L. cv. Nipponbare. The CYP72A18 cDNA was cloned from rice and heterologously expressed in Saccharomyces cerevisiae AH22 cells from the alcohol dehydrogenase (ADH1) promoter. Microsomes isolated from recombinant yeast cells contained the CYP72A18, which was found to catalyze the (ω-1)-hydroxylation of the herbicide pelargonic acid. We also show that (ω-1)-hydroxypelargonic acid has reduced herbicide activity against rice seedlings. Based on these results, we suggest that CYP72A18 participates in the detoxification of the herbicide pelargonic acid in rice plants.     

广东省水稻田稗对五氟磺草胺的抗性分析

为明确广东省水稻田杂草稗Echinochloa crus-galli对五氟磺草胺的抗性现状及其可能的抗性机理，采用整株剂量反应法测定不同地区稗种群对五氟磺草胺的抗性水平，对不同稗种群的乙酰乳酸合成酶（acetolactate synthase，ALS）基因片段进行扩增测序，分析细胞色素P450酶（cytochrome P450 monooxygenase，P450）和谷胱甘肽-S-转移酶（glutathione-S-transferase，GST）抑制剂胡椒基丁醚（piperonylbutoxide，PBO）和4-氯-7-硝基-2，1，3-苯并氧杂噁二唑（4-chloro-7-nitro-1，2，3-benzoxadiazole，NBD-Cl）对不同稗种群抗性水平的影响，并对替代药剂进行筛选。结果显示，广东省水稻田多数稗种群对五氟磺草胺仍表现敏感，但采自湛江市的1个种群BC-7对五氟磺草胺产生了抗性，抗性倍数达6.5倍。与敏感种群BC-2相比，BC-7种群并未发生已报道的ALS靶标抗性相关突变。PBO和NBD-Cl均可显著提高BC-7种群对五氟磺草胺的敏感性，其干重抑制中量GR₅₀由31.1 g/hm²分别降为11.0 g/hm²和24.7 g/hm²。BC-7种群对氰氟草酯和噁唑酰草胺仍较敏感，但对二氯喹啉酸和双草醚产生了抗性。表明P450和GST介导的代谢抗性是稗BC-7种群产生抗性的重要原因，氰氟草酯和噁唑酰草胺适用于治理该抗性种群。     

Chemical control of weedy rice in precise hill‐direct‐seeded rice in South China

Precise hill‐direct‐seeded rice, which is both cost‐ and labor‐saving, is based on the direct seeding of rice by using a precision rice hill‐drop drilling machine. Weedy rice (Oryza sativa f. spontanea), also known as “red rice”, is a major weed in precise hill‐direct‐seeded rice, causing an ≤80% yield loss and a reduction in grain quality. The aim of this study was to evaluate the control efficiency of weedy rice by pretilachlor (a pre‐emergence herbicide) and fenclorim (a safener) and their safety for precise hill‐direct‐seeded rice in two consecutive years. The amount of rice seed germination was accelerated by soaking the seeds in the safener at 0.67 g ai L^?1 for 1 h before sowing. The pre‐emergence pretilachlor treatments were applied 2 days after sowing cultured rice. The inhibition of the shoot fresh weight of the cultured rice was reduced by 3.3, 6.4 and 7.4% with 450, 900 and 1350 g ai ha^?1 of pretilachlor at 32 days after sowing (DAS) and that of the root fresh weight was reduced by 2.6, 4.9 and 8.1%, respectively. With fenclorim and pretilachlor in a precise hill‐direct‐seeded rice field in 2010 and 2011, the weedy rice control efficiency at 32 DAS was reduced by 100 and 98.0%, respectively. The pre‐emergence pretilachlor treatments that were applied at 2 DAS were much more efficient in the weedy rice control and less inhibitory to the cultured rice growth. The rice yield was increased by 26.1–26.7% in the mechanical precise hill‐direct‐seeded rice, relative to the manual‐seeding rice, with the application of fenclorim and pretilachlor.     

细胞色素P450抑制剂对白腐菌Phlebia lindtneri降解氯丹的影响

为确定细胞色素P450酶系在白腐菌Phlebia lindtneri降解有机氯类农药氯丹中的作用,在液体培养条件下,以胡椒基丁醚和1-氨基苯并三唑作为细胞色素P450的抑制剂,分析了不同浓度抑制剂对氯丹的降解、代谢产物的生成以及中间代谢物降解的影响。结果表明:与对照相比,高浓度(1.0 mmol/L)胡椒基丁醚或1-氨基苯并三唑处理15 d后氯丹的降解率均下降了约60%,且其代谢产物中除七氯和二氯代六氯的检出量显著增加外,其余环氧化及羟基化代谢产物均未检出;此外,添加高浓度的抑制剂可导致白腐菌降解中间代谢产物七氯及二氯代六氯的降解率下降90%以上,氧化氯丹的降解率下降70%以上,但不影响环氧七氯的降解。表明细胞色素P450可能是氯丹降解的主要酶系,其参与催化了氯丹的初始羟基化和水解、七氯和二氯代六氯的环氧化及氧化氯丹的水解等多个反应过程。     

Inhibition of thiazopyr metabolism in plant seedlings by inhibitors of monooxygenases

Metabolism of the herbicide thiazopyr [methyl 2-(difluoromethyl)-5-(4, 5-dihydroO-lhiazo!vt)-4-(2-methylpropy!)-6-(trinuorornethyl)-3-pyridinecarboxy-late] was examined in young seedlings of redroot pigweed, grain sorghum, sunflower, corn and soybean. As previously observed with rat liver microsomes plants predominantly metabolized thiazopyr via oxidation reactions. Sulfur and carbon atoms in the thiazoline ring were the primary sites of plant oxygenases. De-esterification was also identified as an important pathway of transformations in plants. Although similar pathways of thiazopyr metabolism were observed among plants, our data indicated species differences in rates of thiazopyr degradation. Among species examined, pigweed (Amaranthus retroflexus L.) showed the fastest metabolism. Thiazopyr metabolism in pigweed was significantly inhibited by several cytochrome P450 monooxygenase inhibitors, among which tetcyclacis (TET) and piperonyl butoxide (PBO) were the most inhibitory. Thiazopyr metabolism in pigweed was not inhibited by organophosphates, known inhibitors of esterases. The results suggest that thiazopyr metabolism in plants is predominantly mediated via plant mono-oxygenases.     

Cross‐resistance study and biochemical mechanisms of thiamethoxam resistance in B‐biotype Bemisia tabaci (Hemiptera: Aleyrodidae)

BACKGROUND: B‐biotype Bemisia tabaci (Gennadius) has invaded China over the past two decades. To understand the risks and to determine possible mechanisms of resistance to thiamethoxam in B. tabaci, a resistant strain was selected in the laboratory. Cross‐resistance and the biochemical mechanisms of thiamethoxam resistance were investigated in the present study. RESULTS: A 66.3‐fold thiamethoxam‐resistant B. tabaci strain (TH‐R) was established after selection for 36 generations. Compared with the susceptible strain (TH‐S), the selected TH‐R strain showed obvious cross‐resistance to imidacloprid (47.3‐fold), acetamiprid (35.8‐fold), nitenpyram (9.99‐fold), abamectin (5.33‐fold) and carbosulfan (4.43‐fold). No cross‐resistance to fipronil, chlorpyrifos or deltamethrin was seen. Piperonyl butoxide (PBO) and triphenyl phosphate (TPP) exhibited significant synergism on thiamethoxam effects in the TH‐R strain (3.14‐ and 2.37‐fold respectively). However, diethyl maleate (DEM) did not act synergistically with thiamethoxam. Biochemical assays showed that cytochrome P450 monooxygenase activities increased 1.21‐ and 1.68‐fold respectively, and carboxylesterase activity increased 2.96‐fold in the TH‐R strain. However, no difference was observed for glutathione S‐transferase between the two strains. CONCLUSION: B‐biotype B. tabaci develops resistance to thiamethoxam. Cytochrome P450 monooxygenase and carboxylesterase appear to be responsible for the resistance. Reasonable resistance management that avoids the use of cross‐resistance insecticides may delay the development of resistance to thiamethoxam in this species. Copyright © 2009 Society of Chemical Industry     

Molecular cloning and characterization of the cinnamate 4‐hydroxylase gene from Eupatorium adenophorum

Cinnamate‐4‐hydroxylase (CA4H), a cytochrome P450‐dependent monooxygenase, plays crucial roles in phenylpropanoid metabolism and plant defense. Previously, the authors showed that the expression of CA4H was induced in response to an allelopathic substance in Eupatorium adenophorum. Here, the full‐length cDNA of EaCA4H was cloned by using rapid amplification of cDNA ends. The 1518 bp open reading frame of EaCA4H was deduced to encode a protein of 505 amino acid residues. Like other CA4H proteins, the predicted EaCA4H polypeptides contained conserved domains of cytochrome P450. A Southern blot analysis indicated that at least five copies of EaCA4H exists in the genome of E. adenophorum. Subcellular localization revealed nuclear‐localized EaCA4H–green fluorescent protein fusion protein in onion epidermal cells. Heterologous silencing of endogenous CA4H in tobacco by a conserved EaCA4H fragment resulted in reduced expressions of key enzymatic genes and the production of downstream flavonoids in the phenylpropanoid pathway. Intriguingly, similar effects were observed in transgenic tobacco plants overexpressing EaCA4H. Altogether, the results indicate that the disturbed expression of CA4H in plants leads to relatively low expression levels of key enzymatic genes and the accumulation of the flavonoids that are involved in phenylpropanoid metabolism.     

Piperonyl butoxide-mediated inhibition of cytochrome P450-catalysed insecticide metabolism: a rational approach

The inhibitory effect of piperonyl butoxide (PBO) on cytochrome P450 was studied by theoretical methods. Binding conformations of PBO were obtained by the recently developed low-mode conformational search within the active site of cytochrome P450_cam. Increased activity of PBO relative to other methylendioxyphenyl inhibitors was rationalized by its decreased conformational mobility and the steric block created by its long side-chain in the substrate access channel of the enzyme. © 1999 Society of Chemical Industry     

Penoxsulam‐resistant barnyardgrass (Echinochloa crus‐galli) in rice fields in China

Barnyardgrass (Echinochloa crus‐galli) proliferation seriously threatens rice production worldwide. Whole‐plant bioassays were conducted in order to test the sensitivity to penoxsulam of 52 barnyardgrass populations and the resistance of six penoxsulam‐resistant populations to 12 other herbicides that are commonly used in rice fields. Among the 48 populations that had escaped penoxsulam control in the rice fields, 8.3% showed a very high level of resistance, 58.3% showed a high level of resistance and 10.4% showed a moderate level of resistance. Multiple resistance was confirmed in all six penoxsulam‐resistant populations that were tested further. They exhibited at least a moderate level of resistance; that is, to 6–10 of the total of 13 herbicides that was tested. Most of the six penoxsulam‐resistant populations showed at least a moderate level of resistance to bispyribac‐sodium, quinclorac, metamifop, cyhalofop‐butyl and oxadiazon, three populations held at least a moderate level of resistance to oxyfluorfen and pretilachlor, two populations also held at least a moderate level of resistance to pyrazosulfuron‐ethyl, pyribenzoxim and fenoxaprop‐P‐ethyl, but the resistance indices of the six populations to pendimethalin were all low. This study has confirmed resistance to pretilachlor and oxadiazon in weeds for the first time.