喹草酮与辛酰溴苯腈复配应用于小麦田的除草效果及对小麦的安全性

为明确新型除草剂喹草酮应用于小麦田的除草效果及对小麦的安全性,在温室内采用共毒系数法对喹草酮与辛酰溴苯腈联合作用进行测定,并验证喹草酮与辛酰溴苯腈两者混用以及与双氟磺草胺三者混用时对小麦田杂草的防效,以及对小麦的安全性。温室试验结果表明,喹草酮对阿拉伯婆婆纳Veronica persica防效优,试验剂量下全部死亡,对播娘蒿Descurainia sophia和麦家公 Lithospermum arvense的GR₅₀分别为12.67 g （a.i.）/hm²和152.99 g （a.i.）/hm²;辛酰溴苯腈对播娘蒿和麦家公防效优,其GR₅₀分别为26.22 g （a.i.）/hm²和13.36 g （a.i.）/hm²,对阿拉伯婆婆纳防效略差,GR₅₀为85.12 g （a.i.）/hm²。喹草酮与辛酰溴苯腈按有效成分用量1：1~1：2.5配比时,阿拉伯婆婆纳全部死亡,对播娘蒿的共毒系数在140.34~202.77之间,呈明显增效作用,对麦家公的共毒系数达700.00以上,也呈明显增效作用。田间试验结果表明,喹草酮对阿拉伯婆婆纳防效高,而对猪殃殃Galium aparine和播娘蒿略差;辛酰溴苯腈作用速度快,但后期部分杂草返青,喹草酮与辛酰溴苯腈复配后优势互补,对小麦田阔叶杂草阿拉伯婆婆纳、猪殃殃和播娘蒿防效均优,鲜重防效在88.54%~ 93.83%之间,且杂草死亡速度快,在2种药剂基础上加入双氟磺草胺后,鲜重防效在96.12%以上。喹草酮单剂或与辛酰溴苯腈、双氟磺草胺的混配处理不影响小麦的正常生长。     

Recovery of non-target plants affected by airborne bromoxynil-octanoate and metribuzin

The present study was conducted to evaluate the recovery potential of non‐target plants affected by two airborne herbicides. Sunflower at the two‐leaf stage was used as a test plant and exposed for 24 h in a wind tunnel to a range of concentrations of airborne bromoxynil‐octanoate and metribuzin. Quantum yield (φ_PSII) of exposed leaves and of the second leaf pair developed after exposure was determined at a particular time up to 16 days following exposure. Maximum depression in quantum yield of exposed leaves from which a complete recovery occurred within 16 days was 63% for bromoxynil‐octanoate and 60% for metribuzin respectively. The corresponding maximum concentrations were 1.310 and 0.390 μg m^?3 respectively. The second leaf pair was also affected and showed a similar recovery potential. From the results it can be concluded that the significance of airborne bromoxynil‐octanoate and metribuzin must not be overestimated, as sunflower and non‐target plants with a similar sensitivity are likely to recover from air concentrations of both herbicides reported under field conditions.     

An analytical procedure for bromoxynil and its octanoate in soils; persistence studies with bromoxynil octanoate in combination with other herbicides in soil

A method is described for the analysis of the herbicide bromoxynil and its octanoate in soils. Following extraction with aqueous acidic acetonitrile, the octanoate was separated from the phenolic bromoxynil by solvent partitioning. The ester and the phenol were assayed by gas-liquid chromatography without further modification or preparation of a derivative. Recoveries in excess of 93% were obtained from soils treated with the phenol and the ester at levels of 0.5 or 0.1 μg g^?1. The persistence of bromoxynil octanoate applied at a rate of 3 μg g^?1 was studied in the laboratory on a heavy clay and a sandy loam at 85% of field capacity moisture and 20°1°C, both alone and in the presence of 2,4-D (2 μg g^?1); MCPA (2 μg g^?1); MCPA+asulam (both at 2 μg g^?1); and MCPA+difenzoquat (both at 2 μg g^?1). In each soil there was a rapid conversion of bromoxynil octanoate to the free phenol, which then underwent a rapid degradation, so that after 7 days, over 90% of the original treatment had disappeared. There appeared to be no effect on bromoxynil breakdown by any of the herbicides added in combination. Small field plots were treated, in early May 1977 and 1978 at two locations in Saskatchewan, with a combination of commercial formulations containing asulam, bromoxynil octanoate, and MCPA at rates of 1 kg ha^?1 each. After 10 weeks the plots were sampled and analysis showed that in all cases, no asulam, bromoxynil, or bromoxynil octanoate could be extracted from the top 10 cm of soil.     

Radiochemical distribution and decline studies with bromoxynil octanoate in wheat

Bromoxynil octanoate labelled with ¹⁴C in the ring or in the cyano-group was applied to wheat seedlings at the two-leaf or fully-tillered stage and at rates equivalent to up to 16 oz a.i./acre. The plants were grown either in environmental chambers under controlled conditions for up to 28 days, or outdoors under field conditions for various periods up to harvest. Initially, elimination of radioactivity occurred more rapidly with bromoxynil-cyano-[¹⁴C]-octanoate than with bromoxynil-ring-[¹⁴C]-octanoate, indicating metabolic attack on the cyano group. Under outdoor conditions with ring-[¹⁴C]-herbicide applied at the two-leaf stage, only 12% of the radioactivity was retained after 28 days, principally in the treated leaves. When application was made at fully-tillered stage, about 33% of the ¹⁴C was retained after 56 days, almost entirely in the treated senescent leaves at the base of the plant. There was very little translocation of the herbicide or of any major metabolite. The level of radioactivity in harvested grain and in straw more than 7.5 cm above the ground was very low, even after very late application of ring-[¹⁴C]-labelled herbicide. The amount of bromoxynil octanoate, together with any metabolite retaining part of the aromatic ring, did not collectively exceed the equivalent of approx. 0.01 parts/million bromoxynil octanoate.     

Spectral and time-resolved fluorescence signature of four weed species as affected by selected herbicides

In the present study we show for the first time the suitability of the laser-induced fluorescence technique to evaluate in vivo herbicide-induced damages as revealed by changes of fluorescence spectra and lifetime. Four herbicides of different modes of action (glyphosate, bromoxynil, mesotrione, and amitrole) were selected and applied to four weed species (Stellaria media, Setaria viridis, Chenopodium album, and Viola arvensis). Modifications of the fluorescence signature depended on the agrochemical – plant species interaction as well as on the time after application. Measurements in the red and far-red spectral region reveal disturbances in the functionality of the photosynthetic apparatus and chlorophyll concentration, e.g. after application of bromoxynil or mesotrione. Recordings in the blue and green spectral regions indicate changes of both amount and composition of specific fluorophores, i.e. after application of glyphosate and amitrole. In all spectral measurements, the position of peak maxima was not affected by herbicide application. The fluorescence lifetime, expressed as LTmean or as lifetime 1 (LT1, short-duration) and LT2 (long-duration) fractions, provided additional information to the spectrally resolved data. Thereby, significant alterations of the lifetime duration and fractional characteristics were observed at specific wavelengths, e.g. after application of bromoxynil, mesotrione, or amitrole.     

Perfusion studies with bromoxynil octanoate in soil

The breakdown of bromoxynil octanoate in 5 different soil types has been studied in a soil perfusion apparatus using herbicide labelled with ¹⁴C either in the cyano group or in the aromatic ring. Even when applied at rates equivalent to 5 to 25 times those used commercially, the herbicide was fairly rapidly and extensively degraded at 15°. After 12 to 13 weeks, up to 80% of the radioactivity in the ¹⁴CN group and up to 63 % of the ¹⁴C in the ring were liberated as carbon dioxide. A small proportion (16 to 19%) of the radioactivity from ring-labelled herbicide remained attached to the soil, probably not as the original herbicide, but in a form not readily leached. Only trace quantities of 3,5-dibromo-4-hydroxy-benzamide (0.5%) and 3,5-dibromo-4-hydroxybenzoic acid (0.1%) were detectable during these soil perfusions.     

Bromoxynil degradation in a Mississippi silt loam soil

BACKGROUND: The objectives of these laboratory experiments were: (1) to assess bromoxynil sorption, mineralization, bound residue formation and extractable residue persistence in a Dundee silt loam collected from 0–2 cm and 2–10 cm depths under continuous conventional tillage and no‐tillage; (2) to assess the effects of autoclaving on bromoxynil mineralization and bound residue formation; (3) to determine the partitioning of non‐extractable residues; and (4) to ascertain the effects of bromoxynil concentration on extractable and bound residues and metabolite formation. RESULTS: Bromoxynil K_d values ranged from 0.7 to 1.4 L kg^?1 and were positively correlated with soil organic carbon. Cumulative mineralization (38.5% ± 1.5), bound residue formation (46.5% ± 0.5) and persistence of extractable residues (T_1/2 < 1 day) in non‐autoclaved soils were independent of tillage and depth. Autoclaving decreased mineralization and bound residue formation 257‐fold and 6.0‐fold respectively. Bromoxynil persistence in soil was rate independent (T_1/2 < 1 day), and the majority of non‐extractable residues (87%) were associated with the humic acid fraction of soil organic matter. CONCLUSIONS: Irrespective of tillage or depth, bromoxynil half‐life in native soil is less than 1 day owing to rapid incorporation of the herbicide into non‐extractable residues. Bound residue formation is governed principally by biochemical metabolite formation and primarily associated with soil humic acids that are moderately bioavailable for mineralization. These data indicate that the risk of off‐site transport of bromoxynil residues is low owing to rapid incorporation into non‐extractable residues. Published 2009 by John Wiley & Sons, Ltd     

In vitro activity and binding characteristics of the hydroxybenzonitriles in chloroplasts isolated from Matricaria inodora and Viola arvensis

The electron transport inhibition, uncoupling, and binding of ioxynil and bromoxynil salts is compared in chloroplast fragments isolated from two weed species with contrasting responses to the hydroxybenzonitriles. Ioxynil Na was three to four times more inhibitory than bromoxynil K towards DCPIP and SiMo reduction in both Matricaria inodora and Viola arvensis. Ioxynil Na was also a more potent uncoupler of PSI-dependent electron transport from ascorbate/DCPIP to methyl viologen. Uncoupling occurred at concentrations higher than those that inhibited electron transport. Binding studies with [¹⁴C]bromoxynil K and [¹⁴C]ioxynil Na salts revealed slightly biphasic curves with no significant difference in the amounts of the two herbicides bound at a given concentration. The ratios of inhibition constant (K_i) and binding constant (K_b) were approximately one for ioxynil Na and three for bromoxynil K. Radiolabelled herbicide displacement studies revealed that ioxynil Na could partially displace bound [¹⁴C]bromoxynil K, but bromoxynil K could not displace bound ioxynil Na at biochemically active concentrations. Ioxynil Na may be a more effective inhibitor than bromoxynil K because it binds more strongly to the thylakoid membrane.     

Physiological basis for antagonism induced by mixtures of quizalofop-ethyl and bromoxynil in maize (Zea mays)

In this study, the physiological basis for antagonism induced by mixtures of quizalofop‐ethyl and bromoxynil was investigated in maize seedlings. In sequential applications, antagonism was observed when bromoxynil was applied before quizalofop‐ethyl or in a mixture with quizalofop‐ethyl, but was minimal when bromoxynil was applied afterwards. The degree of antagonism differed with application rates of bromoxynil and with the timing of the treatment. When test herbicides were applied locally to the second leaf, the inhibition of photosystem II (PS‐II) in the herbicide‐treated leaf was higher with the mixture than with bromoxynil or quizalofop‐ethyl alone. Subsequent growth of the untreated third leaf inhibited by quizalofop‐ethyl alone then recovered, depending on the dose of bromoxynil. There was no evidence that bromoxynil affected absorption of quizalofop‐ethyl. In local applications at different positions on the second leaf, antagonism was only observed when quizalofop‐ethyl was applied to the distal part of the leaf and bromoxynil applied to the proximal part. The antagonism of bromoxynil + quizalofop‐ethyl did not occur at the level of acetyl CoA carboxylase and Hill reaction, as revealed by in vitro assays. These results suggest that bromoxynil inhibits the phloem transport of quizalofop‐ethyl and thus antagonises its whole‐plant activity in maize.     

Leaf chlorophyll fluorescence discriminates herbicide resistance in Echinochloa species

Timely detection of herbicide resistance at an early stage of crop cultivation is essential to help farmers find alternative solutions to manage herbicide resistance in their fields. In this study, maximum quantum yield of PS II [F_v/F_m = (F_m – F_o)/F_m] was measured at the 4–5 leaf stage to discriminate between herbicide‐resistant and susceptible biotypes of Echinochloa species. The differences in F_v/F_m between herbicide‐resistant and susceptible Echinochloa spp. were consistent with the whole‐plant assay based on I₅₀ (herbicide doses causing a 50% inhibition of F_v/F_m) and GR₅₀ (herbicide doses causing a 50% reduction in plant fresh weight) values and R/S ratios (herbicide resistance index), regardless of the mode of action of the tested herbicides. A PS II inhibitor caused the fastest inhibition of F_v/F_m, compared with ACCase and ALS inhibitors, after herbicide treatment. The required time for discrimination between herbicide‐resistant and susceptible Echinochloa spp. was 64 h after PS II inhibitor treatment, much shorter than those of ACCase and ALS inhibitor‐treated plants, which required 168 and 192 h respectively. The leaf chlorophyll fluorescence assay provided reliable diagnostics of herbicide resistance in Echinochloa spp. with significant time savings and convenient measurement in field conditions compared with the conventional whole‐plant assay.     

Effect of climatic factors on the potency of ioxynil and bromoxynil

Outdoor pot experiments, carried out between 1967 and 1971, mainly with Polygonum lapathifolium L. and Stellaria media (L.) Vill., showed that herbicidal potency of ioxynil and bromoxynil salts and esters was affected by climatic conditions, particularly solar radiation and relative humidity. Multiple regression equations were frequently obtained which accounted for 80% or more of the observed variation in effective dose (ED₉₀). By contrast, experiments in growth cabinets suggested that air temperature was the most important climatic variable; the reasons for this disagreement are discussed. It is concluded that climatic factors affect the potency of ioxynil and bromoxynil via their influence on leaf uptake; ester formulations (emulsions) were much less affected than aqueous salt solutions.     

Metabolism of bromoxynil octanoate in growing wheat

[¹⁴C]ring-Bromoxynil octanoate was applied to the leaves of wheat seedlings, which were cultivated in a growth cabinet under controlled conditions for 14 days. Fractionation of the metabolites present in the treated leaves, which accounted for about 63% of the radioactivity applied, indicated a complex metabolic pathway resulting from initial hydrolysis to free bromoxynil, followed by three consecutive or concurrent steps (a) hydrolysis of the cyano group to the amide and carboxylic acid, followed by decarboxylation to 2,6-dibromophenol (0.5% of the ¹⁴C applied), (b) replacement of one or both bromine atoms by hydroxy groups to 3-bromo-4,5-dihydroxybenzonitrile (1.3 %) and 3,4,5-trihydroxybenzo-nitrile (0.6 %) or their hydrolysis products, (c) replacement of one or both bromine atoms by hydrogen, giving 3-bromo-4-hydroxybenzonitrile (1.9 %) and 4-hydroxy-benzonitrile (0.6%) or their hydrolysis products. Some of the phenolic acids or phenols formed are natural plant constituents. The metabolites identified represented in all about 11 % of the herbicide applied, but no individual metabolite accounted for more than a small proportion of it.     

Intercalation of the herbicide atrazine in layered double hydroxides for controlled-release applications

BACKGROUND: The herbicide atrazine was intercalated in the interlayer region of Mg/Al layered double hydroxides in order to produce a nanohybrid that could be used in controlled‐release applications. RESULTS: The hydrophobic herbicide was incorporated in artificial membranes formed in the interlayer of the inorganic host by using palmitic acid. The synthetic nanohybrid material was characterised by various techniques, and release studies were carried out. In addition, the photosynthetic alga Chlamydomonas reinhardtii Dang. was treated with the atrazine‐containing nanohybrid, which exerted an herbicidal efficacy similar to that of the free herbicide. CONCLUSION: The herbicide containing nanohybrid could enable a controlled release of the herbicide. In addition, the herbicide would be delivered close to its site of uptake, enhancing efficiency and reducing the required doses. Copyright © 2011 Society of Chemical Industry     

Biodegradation of the herbicide bromoxynil and its plant cell wall bound residues in an agricultural soil

The mineralization and formation of metabolites and nonextractable residues of the herbicide [¹⁴C]bromoxyniloctanoate ([¹⁴C]3,5-dibromo-4-octanoylbenzonitrile) and the corresponding agent substance [¹⁴C]bromoxynil ([¹⁴C]3,5-dibromo-4-hydroxybenzonitrile) was investigated in a soil from an agricultural site in a model experiment. The mineralization of maize cell wall bound bromoxynil residues was also investigated in the agricultural soil material. The mineralization of [¹⁴C]bromoxynil and [¹⁴C]bromoxyniloctanoate in soil within 60 days amounted up to 42 and 49%, respectively. After the experiments, 52% of the originally applied [¹⁴C]bromoxynil and 44% of the [¹⁴C]bromoxyniloctanoate formed nonextractable residues in soil. Plant cell wall bound [¹⁴C]bromoxynil residues were also mineralized to an extent of about 21% within 70 days; the main portion of 76% persisted as nonextractable residues in the soil. In bacterial enrichment cultures and in soil two polar metabolites were observed; one of it could be identified as 3,5-dibromo-4-hydroxybenzoate and the other could be described tentatively as 3,5-dibromo-4-hydroxybenzamide.     

Efficacy of four corn (Zea mays L.) herbicides when applied with flat fan and air induction nozzles

Twelve field experiments were conducted over a 4 year (2002–2005) period to determine the influence of the herbicide dose, nozzle type, spray volume, and spray pressure on herbicide efficacy in field corn ( Zea mays L.). The control of Abutilon theophrasti (velvetleaf ), Ambrosia artemisiifolia (common ragweed), Chenopodium album (common lambsquarters), Amaranthus powellii (green pigweed), and Echinochloa crus-galli (barnyard grass) was improved with the use of full herbicide doses compared to half doses of bromoxynil, glufosinate, dicamba, and nicosulfuron. The yield was increased for bromoxynil, glufosinate, and nicosulfuron when the full herbicide dose was used. When applied at the manufacturer's recommended dose, flat fan nozzles, compared to air induction (AI) nozzles, provided better control of A. theophrasti , A. artemisiifolia , and C. album with bromoxynil, A. artemisiifolia and C. album with dicamba, and E. crus-galli with nicosulfuron. Bromoxynil, in relation to weed control, was the only herbicide that was affected by the water carrier volume. By increasing the spray pressure with an AI nozzle, there was an improvement in the control of A. theophrasti , A. artemisiifolia, and C. album with the application of bromoxynil and E. crus-galli with the application of nicosulfuron, with a yield increase with bromoxynil. Overall, this study concludes that the optimum nozzle type, water carrier volume, and spray pressure is herbicide- and weed species-specific.     

Herbicide binding in various mutants of the photosystem II D1 protein of Chlamydomonas reinhardtii

Various mutants of the D1 protein of photosystem II were generated by transforming a Chlamydomonas reinhardtii strain specifically engineered to lack a 0.4 kb fragment in the psbA gene. This mutant is unable to grow photosynthetically. The following mutants were obtained: Asp₁₇₀Glu, Gly₁₇₈Ser, Leu₂₁₈Ser or Thr, Arg₂₃₈Val, Thr₂₄₅Ala or Ser and Ser₂₆₄Lys or Ile. In these mutants, the following herbicides were assayed for their inhibitory activity: triazines, triazinones, ureas, biscarbamates, and phenols. The results indicate that besides Leu₂₁₈ and Ser₂₆₄ also Gly₁₇₈ influences herbicide binding, probably via long-range effects. The herbicide resistances of Ser₂₆₄ mutants have been recognized since a long time. However, substitution of Ser₂₆₄ specifically by Lys exhibit extreme resistance to triazines and triazinones, but no or slight resistance to ureas.     

Chemical control of Eleusine indica and other weeds in Setaria anceps

In field experments on the Altherton Tableland. Queensland. Auslralia, methabenzthiazuron used at 1 2 kg ha pre-emergence was the most effective herbicide for selectively controlling Eleusine indica (L.) Gaertn in seed crops of Setaria anceps Stapf. Bromoxynil. bromoxynil plus MCPA, simazine and terbutryne were either ineffective or phytotoxic to S anceps. A more reliable technique was the use of diuron applied at 2.8 kg ha pre-emergence when the crop row was physically protected with metal shields at spraying or when activated carbon applied as a slurry in water at 168 kg per sprayed ha was sprayed in a 3 cm wide band over the crop row at sowing Three successive applications of paraquat over a 39 day period prior to sowing the crop were necessary for effective control of E. indica using the ‘stale seed bed’ technique     

Hybridisation between wheat and Aegilops geniculata and hybrid fertility for potential herbicide resistance transfer

Hybridisation between wheat and Aegilops geniculata was quantified in a 4‐year crossing experiment in the glasshouse, using three wheat cultivars as pollen donors and herbicide resistance as a phenotypic marker. Hybridisation rates ranged from 5% to 74%. Most of the hybrids were self‐sterile. However, seven F₂ seeds were obtained from 165 A. geniculata–wheat hybrids. Hybrid seeds were found in all backcross (BC₁) combinations at average rates of 4.2% (0–26.3%) and 5.88% (0–34%) under glasshouse and field experiments, respectively, with significant differences among years and cultivars. Wheat cultivars, F₁ and BC₁ plants, were resistant to herbicides while A. geniculata plants were susceptible. In the subsequent generations, although few plants were available, the BC₁F₁ had a certain degree of fertility and the fertility increased in the F₂ plants, with one plant that reached 66.7%. The commercial growing of genetically modified herbicide‐tolerant wheat is expected to have the potential for the inserted gene to escape from the crop and become incorporated in a closely related wild species, conferring a competitive advantage to these conferring weeds. Determining the frequency of crop‐wild transgene flow and the fertility of the formed hybrids is a necessity for risk assessment. Data presented here provide new knowledge on the potential A. geniculata–wheat herbicide resistance transfer.     

Influence of weather on the efficacy of dichlorprop-P/MCPA and trihenuron-methyl

The influence of weather on the efficacy of dichlorprop-P/MCPA and tribenuron-methyl on annual weeds in spritig barley was studied in the field during 4 years at six locations in southern Sweden. The herbicides were applied at one-eighth to three-quarters of the full dose at three application times with approximately 6-day intervals. Weather stations, placed in the experiments, recorded climatic data, Maximum herbicide efficacy was obtained when spraying 1 week after the cotyledon stage with half or three-quarters of the recommended dose. Dose-response curves were estimated and the ED₈₀ doses were calculated. On average, the herbicide dose required to obtain an effect of 80% was about 40% of the recommended dose. The influence of weather was analysed for seven different periods: 7 and 2 days before and after herbicide application, 1 day before and after application, and the day of herbicide treatment. The most pronounced eftects of weather were found for the day of and the day before herbicide application, revealing the strong influence of weather on herbicide uptake and plant metabolism. High air tetnperature and low global radiation during the day of treattnent reduced the ED₈₀ dose of dichlorprop-P/MCPA, whereas the ED₈₀ dose of tribenuron-methyl increased. For both herbicides, precipitation and high soil temperature increased the ED₈₀ dose, which reflects the importance of rain on herbicide uptake and the effect of soil temperature on plant growth. The R² values were higher in the analyses of dichlorprop-P/MCPA than of tribenuron-methyl, indicating that the effect of dichlorprop-P/MCA was more weather-dependent than that of tribenuron-methyl. Separate analyses of the ED₈₀ doses for Brassica napus L., Chenopodium, album L. and Stellaria media (L.) Vill. generally resulted in increased R² values. but otherwise gave results similar to those for the total weed population. Although the analyses revealed significant effects of indivtdual weather factors on herbicide efficacy, it was not possible to discern a consistent and causal relationship between weather and herbicide performance.     

敌草胺在土壤中的吸附及其与持久性和生物有效性之间的关系

土壤吸附是农药在环境中归趋的关键支配因素,也是支配农药在环境中的持久性和生物有效性的重要因素之一。该文采用高效液相色谱法研究了除草剂敌草胺在不同性质土壤中的吸附、持久性和生物有效性以及吸附与土壤持久性、蚯蚓生物有效性之间的关系。结果表明,在供试浓度范围内,采用批量平衡技术测定的敌草胺土壤吸附等温线可用Freundlich模型表征（r>0.99）,土壤有机质含量（PPt50）在61.3-97.6 d之间;微生物对敌草胺在土壤中的持久性影响显著,微生物降解是敌草胺在土壤环境中降解的主要途径,灭菌处理后其在土壤中的半衰期延长了2.09~3.65倍。蚯蚓Eisenia foetida对敌草胺的吸收和生物积累也主要取决于土壤性质,特别是土壤的有机质含量水平（Pr=-0.885,Pr=-0.796,Pt50=94.210-3.535 Kf和BAF=0.264-0.014 Kf,表明吸附系数可用作模型参数来评价敌草胺在土壤中的持久性和生物有效性。