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1.
Due to the presence of an asymmetrically substituted C atom, dimethenamid [2-chloro-N-(2,4-dimethyl-3-thienyl)-N-(2-methoxy-1-methylethyl)acetamide], a recently introduced N-thienyl chloroacetamide herbicide, exists as two stereoisomers (S and R) having differing herbicidal activities as demonstrated with a selection of weeds and Lemna minor. The activity of the two isomers was investigated in greater detail with the green alga Scenedesmus acutus and compared to that of alachlor [2-chloro-N-(2,6-diethylphenyl)-N-(methoxymethyl)acetamide]. As with alachlor, the S isomer (5 μM ) strongly inhibited algal growth and fatty acid desaturation while the R isomer had no effect. In short-term experiments (up to 5·5 h), the S isomer and alachlor (100 μM ) inhibited [14C]acetate uptake and its incorporation into fatty acids in the same manner, while the R isomer did not. Incorporation of [14C]acetate into a non-lipid fraction of the algae was strongly inhibited by alachlor and the S isomer (100 μM ) and only slightly by the R isomer. A 50% inhibition of incorporation of [14C]oleic acid into the same non-lipid fraction was attained with less than 10-7 M of the S isomer while 10-5 M of the R form of dimethenamid achieved only a 40% inhibition. The same stereospecificity of the compound on growth, fatty acid desaturation, acetate uptake and oleic acid incorporation provides strong evidence that dimethenamid may act upon a primary, specific target in lipid metabolism. Furthermore, the comparable biological activities of dimethenamid and alachlor indicate that this target is common to both N-phenyl and N-thienyl chloroacetamide herbicides. © 1997 SCI.  相似文献   

2.
Bioconcentration kinetics of three major paddy-field herbicides, butachlor, thiobencarb and chlomethoxyfen were investigated by accumulation and elimination measurements in laboratory experiments with black silver carp (Aristichthys nobilis). The biological half-lives of the three herbicides on exposure at high and low concentrations were 11·6 and 23·1 days for butachlor, 13·9 and 17·3 days for thiobencarb and 5·6 and 4·5 h for chlomethoxyfen, respectively. One- and two-compartment models were used to elucidate the bioconcentration kinetics. Data from a short-term, 14-day expiry experiment were used to estimate the parameters in the models by non-linear regression analysis, and the bioconcentration factors (BCF) in the steady state were calculated from those parameters. The BCF in the steady state have the descending order thiobencarb > chlomethoxyfen > butachlor at high concentration, and butachlor > thiobencarb > chlomethoxyfen at low concentration. One-compartment model for butachlor and thiobencarb and a two-compartment model for chlomethoxyfen are useful to predict the BCF on prolonged exposure and, further, to assess the influence of these pollutants. © 1997 SCI.  相似文献   

3.
Abstract

Experiments conducted at the International Rice Research Institute (IRRI) in the Philippines, showed that all commonly marketed formulations and derivatives of 2,4-D and MCPA were equally effective in controlling barnyard grass [Echinochloa crusgalli (L.) Beauv.] and other annual weeds in transplanted rice (Oryza sativa L). In the Philippines, these phenoxy acid herbicides cost US$2.50/ha as liquid formulations and US$5.50/ha as granular formulations. These low-cost herbicides provide excellent alternatives to hand weeding in transplanted tropical rice. Other herbicides which can control weeds before or after the weeds emerge are more expensive than 2,4-D or MCPA. Some of these selective herbicides, such as butachlor and TCE-styrene + 2,4-D, are in the Philippine market. Their prices vary from US$8 to US$12/ha.

For direct-seeded flooded rice, granular formulations of several new herbicides, such as butachlor, benthio-carb and C-288 (chemistry not yet disclosed), were highly selective in controlling barnyardgrass and other annual weeds under tropical conditions. C-288 controls algae in addition to annual weeds in direct-seeded flooded rice. Of these three promising herbicides, only butachlor is marketed in the Philippines at US$8/ha. For upland rice, the chemicals which look promising are butachlor, benthiocarb and fluorodifen. Butachlor liquid is available to rice farmers in Asia at about US$16/ha. These herbicides provide an excellent alternative to hand weeding. Generally a complete job of weed control in upland rice requires more than one hand weeding.  相似文献   

4.
The adsorption of metolachlor, acetochlor, pretilachlor and butachlor, as a group of acetanilide herbicides, on eight soils with various physical and chemical properties was studied. The adsorption isotherms fit the Freundlich equation well. The extent of adsorption increased in the order: metolachlor < acetochlor < pretilachlor < butachlor. The product of the Freundlich adsorption constants, Kf(1/n), showed good correlation with organic matter content (OM) of soils for each of these herbicides, suggesting that the latter is the main factor controlling the adsorption process of these acetanilide herbicides. Multivariant correlation regression between Kf(1/n) and two factors, water solubility (Sw) of herbicides and OM, was also performed. Kf(1/n) correlated well with 1/Sw and OM/Sw, showing that high Sw corresponds to a weak tendency to adsorb on soils. IR spectra and ESR parameters confirmed that multifunctional H bonds and charge-transfer bonds between humic acids (HA) and the herbicides were the main adsorption mechanisms of the latter. The ability of herbicides to form these adsorption bonds with HA increased in the same order as the extent of adsorption. © 1999 Society of Chemical Industry  相似文献   

5.
BACKGROUND: With the objective of exploring the herbicidal activity of substituted aurones, a series of 4,6‐disubstituted and 4,5,6‐trisubstituted aurones were synthesised, and their herbicidal activities against Brassica campestris L. and Echinochloa crusgalli (L.) Beauv. were evaluated in laboratory bioassays. Effects of some of the compounds were evaluated on seed germination. The most active compounds in the laboratory were evaluated in the greenhouse. RESULTS: The compounds were characterised by 1H NMR, 13C NMR and HRMS; some of them were further identified by IR. A (Z)‐configuration was assigned to the aurones, based on spectroscopic and crystallographic data. Bioassay results of root growth showed that the aurones had a moderate herbicidal activity against the dicotyledonous plant Brassica campestris. (Z)‐2‐Phenylmethylene‐4,6‐dimethoxy‐3(2H)‐benzofuranone(6o) was the most active compound, with 81.3 and 88.5% inhibition at 10 and 100 µg ml?1 respectively, equal to the activity of mesotrione. Some of the aurones possessed some inhibition of germination on several plant species. For glasshouse tests, the substituted aurones had lower herbicidal activity than metolachlor and mesotrione. CONCLUSION: It is possible that aurone derivatives, which possess structures different from those of the commercial herbicides, may become novel lead compounds for the development of herbicides against dicotyledonous weeds with further structure modification. Copyright © 2012 Society of Chemical Industry  相似文献   

6.
Several ethyl 2,3-dihydro-3-oxoisothiazolo[5,4-b]pyridine-2-alkanoate derivatives were synthesized as herbicides. Only 5-methyl derivatives inhibited both hypocotyl and root growth in the lettuce (Lactuca sativa L.) seedling test at 100 mg litre-1. Only ethyl propionate and valerate derivatives showed significant inhibition at 0·1 mg litre-1, whereas ethyl acetate or butyrate derivatives were inactive. Contrary to unoxidized derivatives, the inhibitory effect of 1-oxide and 1,1-dioxide derivatives was strongly dependent on concentration; ethyl 2,3-dihydro-5-methyl-3-oxoisothiazolo[5,4-b]pyridine-2-propionate 1,1-dioxide inhibited 100% of germination at 100 mg litre-1 and 45% of lettuce seedling growth at 0·1 mg litre-1. Quantitative structure–inhibition of growth relationship analysis carried out by adaptive least-squares (ALS) method gave a good correlation with small and hydrophobic 5-substituents as well as with odd carbon-chain ethyl alkanoates in position 2. Active compounds did not show auxin-like activity from 0·1 to 100 mg litre-1. © 1997 SCI.  相似文献   

7.

Two-way effects of herbicide on rice resistance and multiplication and feeding of the rice brown planthopper (BPH), Nilaparvata lugens (Stål) were studied. Four of 11 herbicides tested, butachlor, metolachlor, oxadiazon and bentazone, had significantly stimulating effects on multiplication and feeding of BPH. Multiplication times (N 1/N 0) of BPH on the rice treated with the four herbicides were 674, 367, 322 and 311, respectively, while that of N. lugens on the untreated plants was 159. The results of measurements of honeydew production by BPH indicated that the feeding rates of the brown planthoppers increased when the insects fed on the plants treated with bentazone, quinclorac, oxadiazon and quinclorac. Survival rates of N. lugens first to third-instars rose on the rice plants treated with butachlor, bentazone, but that of the fourth and fifth instars were not affected. Furthermore, all of those herbicides tested led to a decline of rice resistance, i.e. the injury scales of the treated plants were larger than that of the control under the same pest stress. Based on their effects on rice resistance and on BPH, the herbicides tested can be divided into two categories, one affecting rice resistance and BPH multiplication, the other affecting rice resistance only.  相似文献   

8.
The potential to mineralize 2,4‐dichlorophenoxyacetic acid (2,4‐D), mecoprop, isoproturon and terbuthylazine was studied in soil and aquifer chalk sampled at an agricultural field near Aalborg, Denmark. Laboratory microcosms were incubated for 258 days under aerobic conditions at 10 °C with soil and chalk from 0.15–4.45 m below the surface. The [ring‐U‐14C]‐labeled herbicides were added to obtain a concentration of 6 µg kg?1 and mineralization was measured as evolved [14C]carbon dioxide. The herbicides were readily mineralized in soil from the plough layer, except for terbuthylazine, which was mineralized only to a limited extent. In the chalk, lag periods of at least 40 days were observed, and a maximum of 51%, 33% and 6% of the added 2,4‐D, mecoprop and isoproturon, respectively, were recovered as [14C]carbon dioxide. Large variations in both rate and extent of mineralization were observed within replicates in chalk. No mineralization of terbuthylazine in chalk was observed. As a measure of the general metabolic activity towards aromatic compounds, [ring‐U‐14C]‐benzoic acid was included. It was readily mineralized at all depths. © 2000 Society of Chemical Industry  相似文献   

9.
The effect of five substituted pyridazinones (pyrazon, San 133-410H, San 9774, norflurazon, and San 6706) on lipid metabolism in groundnut (Arachis hypogaea) leaves was investigated under nonphotosynthetic conditions. In experiments with leaf disks, the uptake of [1-14C]acetate, [32P]orthophosphate, and [35S]sulfate was significantly inhibited by these herbicides and the magnitude of inhibition varied, depending on the substituents. When the incorporation of these precursors into lipids was measured and expressed as percentage of total uptake, no effect was observed in the case of [1-14C]acetate but there was significant inhibition in the incorporation of the other two precursors, suggesting that pyridazinones interfere with the metabolism of the phospholipids and the sulfolipid. None of these compounds affected the uptake of [methyl-14C]choline but all inhibited its incorporation into phosphatidylcholine indicating that phosphatidylcholine metabolism is vulnerable to pyridazinones. The fatty acid synthetase of isolated chloroplasts assayed in the absence of light was inhibited 20–50% by the pyridazinones at 0.1–0.5 mM concentrations. San 9774 showed the most potent inhibition. In addition, the pyridazinone herbicides significantly inhibited sn-glycerol-3-phosphate acyltransferase(s) in both chloroplast and microsomal fractions but showed no effect on phosphatidic acid phosphatase. The magnitude of inhibition of fatty acid synthetase and acyltransferase(s) is related to the nature of the substituent groups on the herbicide. Trifluorophenyl substitution at position 2 or amino substitution at position 5 of the pyridazinone molecule caused the maximum inhibitory effect.  相似文献   

10.
The effects of the herbicide isouron and of its plant degradation products designated as metabolite l {N-[5-(1,1-dimethylethyl)-3-isoxazolyl]-N-methylurea} and metabolite 2 {N-[5-(1,1-dimethylethyl)-3-isoxazolyl]-urea} on the metabolism of enzymatically isolated leaf cells of soybean [Glycine max (L.) Merr., cv. Essex] were compared under laboratory conditions. Photosynthesis, protein synthesis, ribonucleic acid synthesis, and lipid synthesis were assayed by the incorporation of NaH14CO3, [14C]-leucine, [14C]-uracil, and [14C]-acetate, respectively, into the isolated cells. Time-course and concentration studies included incubation periods of 30, 60, and 120 min and concentrations of 0.1, 1, 10 and 100 μM of the three herbicides. The urea derivative of isouron (metabolite 2) was the least active of the three compounds. The activity of the mono-methylated derivative of isouron (metabolite 1) was comparable to that of isouron and the sensitivity of the four processes to both chemicals decreased in the order: photosynthesis > ribonucleic acid synthesis > lipid synthesis > protein synthesis. The concentration of isouron that caused a 50% inhibition of photosynthesis of the isolated soybean leaf cells was calculated at 0.51 μM. The effects of isouron and metabolite 1 on photosynthesis, lipid and RNA synthesis appeared to be independent of incubation lime as maximal inhibition occurred within 30 min. Inhibition of protein synthesis by both chemicals was time-dependent, increasing in magnitude with concomitant increases in incubation time.  相似文献   

11.
三种除草剂对大型溞Daphnia magna存活、生长和繁殖的影响   总被引：1，自引：0，他引：1  
张欣  赵文  徐峰 《农药学学报》2009,11(1):121-125
为了制定除草剂在水环境中的允许浓度和排放标准,参照美国公共卫生协会等编著的《水和废水标准检验法》以及我国制定的大型溞Daphnia magna毒性测定方法,进行了丁草胺、吡嘧磺隆、苄嘧磺隆 3种稻田常用除草剂对大型溞的21 d慢性毒性试验。结果发现:随着除草剂浓度的升高,大型溞的产前发育期、产幼间隔期均缩短,每胎产幼数量先增加后减少;丁草胺各浓度处理组中,内禀增长率(rm)在0.157 2~0.314 0 d-1之间,变化较大;吡嘧磺隆各个浓度组的rm相对平稳, 为0.206 6~0.276 8 d-1;大型溞在苄嘧磺隆处理组中的rm比在其他两种除草剂中的高,为0.334 1 ~0.397 1 d-1。在丁草胺处理组中,大型溞的日生殖量较少,低于吡嘧磺隆和苄嘧磺隆处理组。  相似文献   

12.
为筛选防除雀麦Bromus japonicus的高效除草剂,采用室内生物测定法研究了13种除草剂对雀麦的除草活性及5种除草剂的田间药效试验。结果表明,在田间推荐剂量的低剂量下,氟唑磺隆、啶磺草胺、氟噻草胺、甲基二磺隆、异丙隆、磺酰磺隆、丙苯磺隆7种除草剂对雀麦具有很高的防除效果,21 d鲜重抑制率分别为88.30%、86.32%、83.97%、78.47%、76.76%、72.83%、71.39%,高剂量下的21 d鲜重抑制率达98.57%、95.36%、91.58%、91.46%、89.47%、82.48%、82.20%;其中氟唑磺隆各剂量下的防效较其它除草剂高。而嘧啶肟草醚、苯唑草酮、炔草酯、吡氟酰草胺、唑啉草酯、精噁唑禾草灵6种除草剂对雀麦防效较差。氟唑磺隆、啶磺草胺、氟噻草胺、甲基二磺隆、异丙隆5种除草剂的田间药效试验表明,氟唑磺隆对雀麦防效最高,高剂量下20 d株防效达85.04%,药后40 d株防效和鲜重防效分别达83.94%和84.17%,未见小麦有明显药害症状,建议田间推荐用量为21.00~42.00 g(a.i.)/hm~2。表明雀麦对不同除草剂的敏感性存在差异,在供试的13种除草剂中氟唑磺隆对雀麦防效最高,较为安全,为防除雀麦的理想除草剂。  相似文献   

13.
Dihydrodipicolinate synthase (DHDPS) (EC 4.2.1.52) and dihydrodipicolinate reductase (DHDPR) (EC 1.3.1.26) have attracted much recent attention as potential herbicide targets. DHDPS was feedback-inhibited by (S)-lysine; inhibition was reversible and uncompetitive with respect to both (S)-ASA and pyruvate. Homoserine lactone was a reversible non-competitive inhibitor of DHDPS with respect to both (S)-ASA and pyruvate. (R)-Cysteine sulfinic acid and (S)-glutamic acid were reversible uncompetitive inhibitors of DHDPS with respect to (S)-ASA. (S)-Aspartic acid was a reversible mixed-type inhibitor. Dipicolinic acid was a reversible competitive inhibitor of DHDPR with respect to the substrate (4S)-4-hydroxy-2,3,4,5-tetrahydro-(2S)-dipicolinic acid, as was isophthalic acid. Δ3-Tetrahydroisophthalic acid was a moderate inhibitor of both DHDPS and DHDPR. These compounds represent possible leads in the development of novel herbicides. © 1999 Society of Chemical Industry  相似文献   

14.
Control of Avena fatua (L.) (wild oat) with diclofop methyl applied at 0·7 kg ha?1 at the two-leaf stage and difenzoquat at 0·84 kg ha?1 at the four-leaf stage in wheat (Triticum aestivum L.) under field conditions was good and not affected when either of these herbicides was mixed with 3,6-dichloropicolinic acid as the monoethanolamine salt at 0·14, 0·20 or 0·30 kg ha?1. In the glasshouse, mixtures containing 3,6-dichloropicolinic acid at rates as high as 0·6 kg ha?1 also did not affect control of A. fatua. When barban at 0·35 kg ha?1, or flamprop methyl at 0·56 kg ha?1 was mixed with similar rates of 3,6-dichloropicolinic acid and applied at the two-leaf and four-leaf stage of A. fatua respectively, a reduction in control of A. fatua (antagonism) occurred under both field and glasshouse conditions. The herbicides for control of A. fatua did not influence the fresh weight suppression of C. arvense shoots obtained in the glasshouse with 3,6-dichloropico-colinic acid at 0·3 kg ha?1. Early tolerance of wheat (cv. Neepawa) was acceptable with all mixtures. Wheat yields with diclofop methyl or difenzoquat alone or in mixture with 3,6-dichloropicolinic acid were increased over the yields from the A. fatua-infested control.  相似文献   

15.
Summary. Thiocarbamate herbicides were applied with incorporation devices and new subsurface application equipment on loamy sand at Tifton, Georgia, U.S.A. Subsurface-applied ethyl N,N-dipropylthiolcarbamate (EPTC), S-propyl bulylethylthiocarbamate (pebulate), and S-propyl dipropylthiocarbamate (vernolate) generally gave better control of Cyperus esculentus L. and Richardia scabra St Hil, but injured peanuts more than applications made on the soil surface and then incorporated into the soil. For soil incorporation, the power-driven rotary hoe was generally better than a disc harrow. Depth of subsurface placement critically affected herbicidal activity, especially on Cyperus esculentus; placement 1·5 in. below the soil surface gave more effective control than placement at 5·5 in. Réactions de Cyperus esculentus, de Richardia scabra et de l'arachide mix herbicides à base de thiocarbamate, en relation avec la methode de placement dans le sol  相似文献   

16.
This study has investigated the activity of several herbicide classes at the plant plasma membrane. Two-phase partitioning was used to prepare highly purified plasma membrane vesicles from the monocotyledon weed black-grass (Alopecurus myosuroides Huds.) and the dicotyledon crop sugar beet (Beta vulgaris L. cv. Celt). The purity of the plasma membrane H+-ATPase activity was characterised with respect to inhibitors, pH and substrate specificity. In both species, contamination of the plasma membrane by tonoplast fragments was largely eliminated and chlorophyll was absent. In addition, the plasma membrane H+-ATPase from black-grass and sugar beet exhibited high vanadate sensitivity and a sharp pH profile around 6·5. Subsequently, H+-ATPase activity was assayed in the presence (100 μM ) and absence of four graminicide classes and auxin-type herbicides. Graminicides, including the aryloxyphenoxypropionate diclofop-methyl and the thiocarbamate triallate, inhibited H+-ATPase activity by 50–80% in both species. However, other graminicides, including the cyclohexanediones and the chloroacetamide alachlor, had no affect. Similarly, auxin-type herbicides such as 2,4-D and MCPA did not inhibit H+-ATPase activity. Results are discussed in relation to the proposed mode of action of these herbicides. © 1998 SCI  相似文献   

17.
MATHIASSEN  KUDSK 《Weed Research》1998,38(4):283-289
The activity of fenoxaprop-P-ethyl applied alone or in tank-mixture with different formulations of mecoprop or sulfonylurea herbicides was compared in a series of pot experiments using Avena fatua L. (wild oat) as a test plant. A logistic model was fitted to the results and dose–response curves of fenoxaprop-P-ethyl applied alone and in mixture with the broad-leaved weed herbicides were estimated using non-linear regressions. Tank-mixtures of fenoxaprop-P-ethyl and mecoprop or metsulfuron-methyl were antagonistic. In general, the activity of fenoxaprop-P-ethyl decreased with increasing doses of the broad-leaved herbicides. In mixture with 1200 g a.i. ha?1 mecoprop, doses of fenoxaprop-P-ethyl had to be increased by 60% to 130% (dependent on formulation) to obtain the same effect as when fenoxaprop-P-ethyl was applied alone. Both the active and the inactive isomers of mecoprop were involved in the antagonism, and the ester formulation of mecoprop-P was less antagonistic than the amine formulation. In mixture with the recommended dose of 8 g a.i. ha?1 of metsulfuron-methyl, doses of fenoxaprop-P-ethyl had to be increased by 20% to 110% to obtain the same effect as with fenoxaprop-P-ethyl applied alone. Fenoxaprop-P-ethyl did not lose activity when applied in mixture with recommended doses of chlorsulfuron, tribenuron and amidosulfuron. Antagonism of the sulfonylurea herbicides seemed to be related to the susceptibility of A.?fatua to these herbicides.  相似文献   

18.
Cyclohexane-1,3-diones such as the herbicides cycloxydim, sethoxydim, alloxydim and clethodim are known to be specific inhibitors of the plastid-located acetyl-CoA carboxylase (ACCase) in Poaceae, a key enzyme of de-novo fatty acid biosynthesis in higher plants. Using several new cyclohexane-1,3-dione derivatives and known herbicides, the relationships between chemical structure and enzyme inhibition have been studied. The basic cyclohexane-1,3-dione structure was modified at three different positions. These compounds were tested for inhibition of the de novo fatty-acid biosynthesis in test systems of etioplasts isolated from Avena sativa L. and Hordeum vulgare L. seedlings and also for inhibition of the isolated barley ACCase. The I50 values of these cyclohexane-1,3-diones were determined. The influence of the modification of alkyl chains (length and type of substituent) on the degree of ACCase-inhibition is discussed. Several new compounds were found that were about two orders more active than the known herbicides cycloxydim or sethoxydim in the etioplast and ACCase test systems but not necessarily on the level of whole plants.  相似文献   

19.
The joint action of mixtures of the sulfonylurea herbicides chlorsulfuron, metsulfuron and tribenuron and MCPA as a dimethylamine salt was assessed on Stellaria media L. and Lamium purpureum L. Two statistical analyses, and appropriate experimental designs, were used—the additive dose model (ADM) and the principle of parallel dose-response curves. The ADM analyses revealed that mixtures of the sulfony-lureas and MCPA were less potent than expected on Stellaria while the parallel-line assay analyses showed that activity of the sulfonylurea herbicides on Stellaria and Lamium was reduced in mixtures with MCPA. The antagonism was found to be dependent on the ratio of the two herbicides. Activity decreased with increasing MCPA ratios in the mixtures. Sequential spraying and selective placement of droplets revealed that MCPA only antagonized the sulfonylureas when the herbicides were in physical contact with each other. The benefits of applying both statistical methods when studying the joint action of two herbicides both possessing activity on the test plants are discussed. Action de melanges d'herbicides sulfonylurées et de MCPA L'action de melanges des herbicides sulfonylurées chlorsulfuron, metsulfuron et tribénuron avec le MCPA formulé en sel de diméthylamine, a été etudiée sur Stellaria media L. et Lamium purpureum L. Deux analyses statistiques asso-ciées a deux systèmes expérimentaux appropriés ont été utilisés: le modèle à doses additives (ADM) et le principe du parallélisme des cour-bes dose-effet. Les analyses ADM ont montré que les melanges de sulfonylurées et de MCPA ont été rnoins efficaces qu'attendu sur Stellaria. Les analyses en courbes parallèles ont montré que 1'activité des herbicides sulfonylurées sur Stellaria et Lamium était réduite dans des mélanges avec le MCPA.L'antagonisme dépendait du rapport entre les doses des deux herbicides, 1'activité décroissant avec 1'augmentation du taux de MCPA. Des traitements séquentiels et des dépôts localisés de gouttelettes ont montré que le MCPA n'était an-tagoniste des sulfonylurées que lorsque les herbicides étaient physiquement en contact. L'intérêt est discuté, d'utiliser les deux méthodes statistiques de concert pour étudier les interactions entre deux herbicides actifs sur les plantes test. Gemeinsame Wirkung von Sulfonylharnstoff-Herbiziden und MCPA Die Wirksamkeit von Mischungen der Sulfonyl-hamstoff-Herbizide Chlorsulfuron, Metsulfuron und Tribenuron mil MCPA als Dimethylamin-salz wurde an Stellaria media L. und Lamium purpureum L. bestimmt. Die Versuche wurden so angelegt, um 2 statistische Analysen anzuwen-den: das Additiv-Dosis-Modell (ADM) und das Prinzip paralleler Dosis-Wirkungs-Kurven. Die ADM-Analyse ergab, daß diese Mischungen gegenüber Stellaria weniger wirksam als erwartet waren, während die Parallel-Analyse zeigte, daß die Wirksamkeit der Sulfonylharnstoff-Herbiz-ide in Mischungen mil MCPA gegeniiber den beiden Arten herabgesetzt war. Es ergab sich, daß der Antagonismus vom Verhältnis der Mischungspartner abhängt. Die Wirkung nahm mit steigenden MCPA-Anteilen in den Mischungen ab. In Spritzfolgen und bei separater Applikation zeigte sich, daß MCPA nur dann gegenüber Sulfonylharnstoffe antagonistisch wirkte, wenn sich die Herbizide vermischten. Die Vorzüge der Anwendung der beiden statistischen Methoden zur Untersuchung des gemeinsamen Effektes von 2 Herbiziden ähnlicher Wirkung werden diskutiert.  相似文献   

20.
Imidazolinone herbicides inhibit the first enzyme of branched-chain amino acid biosynthesis, acetohydroxyacid synthase. The inhibition of the enzyme in vitro by these herbicides increases with incubation time, but is not irreversible, as deduced by reaction progress curves. In contrast to this result is the apparent irreversible inhibition of the enzyme by these imidazolinones that occurs when the herbicide is applied to intact corn plants. Plants treated with imidazolinone herbicide and then extracted showed dramatically reduced enzyme activity. This effect on extractable enzyme level occurred with several different imidazolinone herbicides in either foliar or soil application. The decrease in extractable enzyme activity could be observed within four hours after treatment. Herbicides other than imidazolinones did not reduce the extractable enzyme level. These findings suggest that the enzyme- imidazolinone interaction in vivo may be different from the interaction observed in vitro.  相似文献   

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