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1.
Structure-concentration–foliar uptake enhancement relationships between commercial polyoxyethylene primary aliphatic alcohol (A), nonylphenol (NP), primary aliphatic amine (AM) surfactants and the herbicide glyphosatemono(isopropylammonium) were studied in experiments with wheat (Triticum aestivum L.) and field bean (Vicia faba L.) plants growing under controlled-environment conditions. Candidate surfactants had mean molar ethylene oxide (EO) contents ranging from 5 to 20 and were added at concentrations varying from 0·2 to 10 g litre?-1 to [14C]glyphosate formulations in acetone–water. Rates and total amounts of herbicide uptake from c. 0·2–μl droplet applications of formulations to leaves were influenced by surfactant EO content, surfactant hydrophobe composition, surfactant concentration, glyphosate concentration and plant species, in a complex manner. Surfactant effects were most pronounced at 0·5 g acid equivalent (a.e.) glyphosate litre?-1 where, for both target species, surfactants of high EO content (15–20) were most effective at enhancing herbicide uptake: surfactants of lower EO content (5–10) frequently reduced, or failed to improve, glyphosate absorption. Whereas, at optimal EO content, AM surfactants caused greatest uptake enhancement on wheat, A surfactants gave the best overall performance on field bean; NP surfactants were generally the least efficient class of adjuvants on both species. Threshold concentrations of surfactants needed to increase glyphosate uptake were much higher in field bean than wheat (c. 2 g litre?-1 and < 1 g litre?-1, respectively); less herbicide was taken up by both species at high AM surfactant concentrations. At 5 and 10 g a.e. glyphosate litre?-1, there were substantial increases in herbicide absorption and surfactant addition could cause effects on uptake that were different from those observed at lower herbicide doses. In particular, the influence of EO content on glyphosate uptake was now much less marked in both species, especially with AM surfactants. The fundamental importance of glyphosate concentration for its uptake was further emphasised by experiments using formulations with constant a.i./surfactant weight ratios. Any increased foliar penetration resulting from inclusion of surfactants in 0·5 g litre?-1 [14C]glyphosate formulations gave concomitant increases in the amounts of radiolabel that were translocated away from the site of application. At these low herbicide doses, translocation of absorbed [14C]glyphosate in wheat was c. twice that in field bean; surfactant addition to the formulation did not increase the proportion transported in wheat but substantially enhanced it in field bean.  相似文献   

2.
The effects of several nonionic surfactants on [14C]glyphosate mono(isopropylammonium) diffusion across isolated tomato fruit cuticles (Lycopersicon esculentum Mill.) were compared under controlled atmospheric conditions (25°C; 65% R.H.) using a model system consisting of 1-μl droplets applied to isolated cuticles on agar blocks. Rates of diffusion for glyphosate (10 g acid equivalent litre?1 in the applied solution) and overall amounts recovered in underlying agar blocks were influenced by the ethylene oxide (EO) chain length for a homologous nonylphenol surfactant series (10 g litre?1). Glyphosate uptake increased with EO content, reaching an optimum at a mean of 17 EO, then decreasing below control values for surfactants with 40 EO. There was a strong influence of the hydrophobe on glyphosate penetration for different surfactants with similar mean EO content (10 EO). The primary aliphatic amine enhanced penetration the most, followed by the nonylphenol while the aliphatic alcohol showed no improvement on glyphosate transfer across cuticles. Water soprtion was greatly enhanced by a primary aliphatic amine (10 EO) and by a nonylphenol (17 EO). The aliphatic alcohol (10 EO) and a shorter-chained nonylphenol (4 EO) did not significantly enhance water sorption. Comparison of water sorption with glyphosate diffusion across cuticles suggests a strong relationship between the two. Change in solution pH over a limited range had no significant effect. Promotion of cuticular hydration by surfactants may thus play an important role in the enhancement of foliar uptake of water-soluble herbicides such as glyphosate.  相似文献   

3.
The effect of non-ionic nonylphenol (NP) surfactants containing 4–14 ethylene oxide (EO) molecules on the distribution of asulam and diflufenican was investigated in Pteridium aquilinum L. Kuhn and Avena fatua L. The distribution of the herbicides was dependent on the EO content and concentration of surfactant and differed between plant species and herbicide. The surface properties of contact angle, droplet diameter and surface tension were examined. For solutions of asulam, the greatest reductions in contact angle, surface tension and greatest droplet diameter were obtained with surfactants of EO 6.5–10 (at 0.001–0.1%). For solutions of diflufenican, these responses were greatest when applied with surfactant of EO 4. Surfactants of EO 6.5–10 increased the uptake and translocation of [14C]asulam in P. aquilinum, particularly at surfactant concentrations of 0.01 % and 0.1 %. All surfactants increased uptake of [14C]asulam in A. fatua with no significant effects of surfactant EO number or concentration. For both species, there was a positive correlation between the optimum surface characteristics of the herbicide droplets and the uptake of asulam. With diflufenican, greatest uptake and translocation by mature frond tissue of P. aquilinum occurred at the highest concentration of surfactant EO 4; in A. fatua, however, uptake and translocation were not significantly affected by any of the surfactants.  相似文献   

4.
The influence of a number of commercial nonionic polyoxyethylene surfactants on the foliar penetration and movement of two systemic fungicides, ethirimol and diclobutrazol, was studied in outdoor-grown wheat plants at different growth stages and post-treatment temperatures in two consecutive growing seasons. Both fungicides were applied as ca 0·2 μl droplets of aqueous suspension formulations containing 0·5 g litre?1 of 14C-labelled active ingredient; surfactants were added to these suspensions at concentrations ranging from 0·2-10 g litre?1. To achieve optimum uptake of each fungicide the use of surfactants with different physicochemical properties was required. For diclobutrazol, a lipophilic compound, uptake of radiolabel was best with surfactants of low mean molar ethylene oxide (E) content (5-6) but it was necessary to use concentrations of ca 5 g litre?1 to attain this. The surfactant threshold concentration for uptake enhancement of radiolabel from ethirimol formulations (< 2 g litre?1) was much lower than that for diclobutrazol but surfactants with E contents > 10 induced the greatest amount of uptake. For both fungicides, surfactants with an aliphatic alcohol hydrophobe were generally more efficient in promoting their uptake than those with a nonylphenol moiety. The sorbitan-based surfactant ‘Tween 20’ proved to be an effective adjuvant only for the ethirimol formulation; the uptake enhancing properties of the block copolymer ‘Synperonic PE/F68’ were weak. Uptake performance could not be related to the spreading properties of the respective formulations on the wheat leaf surface or to differences in solubilisation of the two fungicides by the surfactants. Although surfactants could substantially increase the amount of acropetal transport of radiolabel from both fungicides, none of those tested specifically promoted it; a constant proportion of the radioactive dose absorbed by a treated leaf was usually exported away from the site of application. The results are discussed in the light of current theories about the mode of action of surfactants as spray adjuvants.  相似文献   

5.
Uptake of pesticides into barley leaves was measured under controlled conditions. Leaves detached from plants were submerged in aqueous solutions of 14C-labelled (2,4-dichlorophenoxy)acetic acid, triadimenol, bitertanol and pentachlorophenol. Uptake was biphasic. A short (30-min) period with high rates of uptake was followed by uptake that proceeded more slowly and was steady over hours. Compartmentation of pesticides was studied by desorbing pentachlorophenol from leaves previously loaded with [14C]pentachlorophenol. From the uptake and desorption kinetics it was concluded that penetration of pesticides proceeds as follows: the compounds are first sorbed at the surface of epicuticular wax aggregates where they are in contact with the donor solutions. Solutes then diffuse through the surface wax aggregates into the cuticle. Equilibrium between donor solutions, surface wax and cuticle is established in about 30 min. After this time the amounts of solutes in these compartments no longer increase. Uptake after this time represents penetration into the leaf cells. This fraction of the pentachlorophenol is retained irreversibly, while that sorbed in wax and cutin can be desorbed again. All compounds were sorbed in cuticular waxes and partition coefficients wax/water were determined. On a mass basis only 5 to 10% of the amounts sorbed in cutin are sorbed in wax. This comparatively low solubility in wax contributes to the barrier properties of cuticular waxes. The other determinant of permeability is the very low mobility of solutes in cuticular waxes.  相似文献   

6.
Surfactants increase the uptake of some foliar-applied chemicals to a greater extent than would be expected from their effects on surface tension and spray coverage. This study of the uptake of 2, 4-D [(2, 4-dichlorophenoxy)acetic acid] evaluated the effect of surfactants on penetration through and sorption by isolated cuticles of apple leaves. [14C]2, 4-D was placed in glass chambers affixed to enzymatically isolated adaxial apple leaf cuticles after the cuticle segments had been treated with various surfactants. The same surfactant pretreatments were included in sorption studies in which cuticle segments were immersed in [14C]2, 4-D for 96 h. Quantities of 2, 4-D passing through or sorbed by the cuticle were determined. Similar experiments were conducted with unaltered cuticles and cuticles dewaxed with chloroform. The hydrophile-lipophile balance (HLB) of polyethylene-glycol-based surfactants was inversely related to the sorption of those surfactants by the cuticles and penetration of 2, 4-D. Sorption of 2, 4-D by apple leaf cuticles was unaffected by surfactant pretreatment. Dewaxed cuticle membranes showed a similar response to 2, 4-D penetration and sorption following the surfactant pretreatment.  相似文献   

7.
The influence of four different wetting agents on the foliar retention, uptake and herbicidal activity of the glutamine synthetase inhibitor, glufosinate, was examined in growth-chamber experiments on barley (Hordeum vulgare L. cv Roland) and barnyard grass (Echinochloa crus-galli (L.) P.B.) as test species. The non-formulated monoammomum salt, glufosinate-ammonium, was applied as a spray, either alone or mixed with a wetting agent. The dose rates of herbicide and wetting agent were 0.5 g a.i. litre?1 and 2.0 g litre?1, respectively, on barnyard grass, and 2.0 g a.i. litre?1 and 60 g litre?1, respectively, on barley. Herbicide damage, rated 10 days after spraying, was greatest when glufosinate was used with a sodium C12/C14-alcohol-diglycolether sulfate (FAEO-sulfate) and least with polyoxyethylene (POE)(8) tridecyl ether; intermediate effectiveness was obtained with a combination of herbicide and a POE(15) tridecyl ether or POE(15)-tallow amine. The activity of the target enzyme, glutamine synthetase, measured 2 h after spraying, was reduced most when FAEO-sulfate was present and least with POE(8) tridecyl ether. The behaviour of the glufosinate wetting agent solutions on plant foliage was analysed by measurements of spray retention, droplet contact angles and foliar uptake of [14C]glufosinate. The results led, for both grass species, to the conclusion that differential ability of the wetting agents to enhance the permeation of glufosinate from the leaf surface deposit into the leaf tissue was the main factor responsible for the differences in herbicidal effectiveness of the glufosinate/wetting agent combinations used in this study.  相似文献   

8.
Penetration of four herbicides (atrazine, diclofop-methyl, dinoseb and glyphosate-mono(isopropylammonium) salt) was followed through isolated pear leaf cuticles into agar and across intact cuticles of Argenteum (ARG) mutant pea leaves from monosized droplets (300 μ diam.) during 48 h following application. Penetration into pea leaves ranged from low for glyphosatemono(isopropylammonium) (5% of amount applied) and atrazine (14%) to rapid for dinoseb (91%) and diclofop-methyl (82%). A major proportion (90%) of the dinoseb retained in the tissues underlying the site of droplet application migrated across the cuticle and the epidermal layer of cells. In contrast, only a small proportion (13%) of the dinoseb entering the leaf was transported to the tissues surrounding the treatment zone. Corresponding values for diclofop-methyl were 61% and 4% respectively. Initially, dinoseb also penetrated rapidly through isolated pear leaf cuticles, 36% of the applied dose being recovered in an agar receiver disc 4 h after treatment, but subsequent uptake was slower. Penetration of glyphosate-mono(isopropylammonium) also decreased after 4 h whereas atrazine and diclofop-methyl diffused steadily through isolated cuticles up to 216 h after treatment. The incorporation of ‘Tween 20’ or ‘Agral 90’ (1 g litre?1) into the formulation reduced the penetration of glyphosate-mono(isopropylammonium) through isolated pear leaf cuticles.  相似文献   

9.
Buffers and leaf discs of mature tobacco (Nicotiana tabacum L.) were utilized to study [14C]-ethylene and 14CO2 evolution from radiolabeled ethephon, (2-chloroethyl)phosphonic acid. Metabolic fate of [14C]ethephon in leaf discs was investigated by use of thin-layer chromatography, high-voltage paper electrophoresis, autoradiography, and liquid scintillation spectroscopy. The evolution of labeled ethylene generally increased with increasing buffer pH, buffer volume, and dosage of [14C]ethephon. [14C]Ethylene was evolved, increasingly with time, from [14C]ethephon either added to the buffer or applied to leaf discs. The rate of [14C]ethylene evolution was maximum during the first day and leveled off on the fourth day. More than 50% of the total [14C]ethylene evolution over a 96-hr period was recovered during the first 24 hr after [14C]ethephon application. No 14CO2 was evolved when [14C]ethephon was degraded in the presence of buffer or leaf discs. Only ethephon itself, and no detectable metabolite thereof, was discovered in the methanolic extract of the leaf disc tissue. An insignificant amount of 14C activity (approximately 2% of the extracted 14C) was detected in the residue. By means of gas chromatography, it was confirmed that in buffers and tobacco leaf tissue ethephon breaks down to release ethylene but not CO2.  相似文献   

10.
J. CORET  A. CHAMEL 《Weed Research》1994,34(6):445-451
The effect of several ethoxylated octylphenols (OP), nonylphenols (NP) and alcohols (AA) on the penetration of [14C]chlorotoluron through isolated box-tree (Buxus sempervirens L.) leaf cuticles was investigated. The herbicide solution was deposited as droplets onto cuticle discs maintained on agar blocks acting as receivers. The effects on chlorotoluron transfer across the cuticles depended on the degree of ethoxylation of the surfactant. For each series, the chlorotoluron transfer was considerably increased by surfactants with low ethylene oxide (EO) content (3 to 6 EO). This effect appeared 24 h after droplet application, then increased with time. It decreased with further increase in the ethoxylation number, and surfactants with a long ethylene oxide chain (OP16, NP20, NP40 and AA20) had no effect. Surfactant concentration (OP5) had a large influence on chlorotoluron transfer; penetration increased sevenfold when OP5 concentration was raised from 0.01 to 10 g l?1. Diffusion of the two tritiated octylphenols, [3H]OP5 and [3H]OP16, was measured simultaneously during chlorotoluron transfer. The diffusion rate of the two surfactants across the cuticles was similar, but a higher amount of OP5 was retained within the cuticle during transfer. Study of the effect of surfactants on the cuticular waxes using differential scanning calorimetry showed that wax begins to melt at a lower temperature in the presence of the nonylphenols NP9 and NP4. Fusion enthalpy was close to -30 J g?1. Effet de quelques alkylphénols et alcools éthoxylés sur la pénétration du [14C]chlortoluron à travers des cuticules végétales isolées Nous avons testé l'effet de plusieurs octylphénols (OP), nonylphénols (NP) et alcools éthoxylés (AA) sur la pénétration du [14C]chlortoluron à travers des cuticules isolées de feuilles de buis. L'herbicide en solution était déposé sous forme de gouttelettes sur des disques de cuticules plaées sur agar. Les effets observés dépendaient du degré d'ethoxylation du surfactant. Pour chaque série, le transfert du chlortoluron à travers les cuticules était considérablement accru avec les surfactants faiblement éthoxylés (3 à 6 oxydes d'éthylène). Cet effet apparaissait 24 h après l'application des gouttelettes puis augmentait avec le temps. Il diminuait avec l'accroissement du nombre d'éthoxylation et aucun effet n'était observé avec les surfactants à longue chaine d'oxydes d'éthylène (OP16, NP20, NP40 et AA20). La concentration en surfactant (OP5) avait une grande influence sur le transfert du chlortoluron dans l'agar, il augmentait sept fois entre 0.01 et 10 g l?1. La diffusion des deux octylphénols (3H-OP5 et 3H-OP16) a été mesurée simultanément durant le transfert du chlortoluron. La vitesse de diffusion des deux surfactants à travers les cuticules était comparable, mais une quantité plus élevée d'OP5 était retenue dans les cuticules durant le transfert. L'étude par analyse calorimètrique à balayage de l'effet des surfactants sur les cires cuticulaires a montré que la fusion des cires commence à plus faible température en présence des nonylphénols NP9 et NP4. L'enthalpie de fusion était en général voisine de -30 J g?1. Wirkung einiger ethoxylierter Alkylphenole und Alkohole auf den Transfer von [14C]Chlortoluron durch die Pflanzen-Cuticula Die Wirkung verschiedener ethoxylierter Octylphenole (OP), Nonylphenole (NP) und Alkohole (AA) auf die Penetration von [14C]Chlortoluron durch die isolierte Blatt-Cuticula von Buxbaum (Buxus sempervirens L.) wurde untersucht. Die Herbizidlösung wurde als Tröpfchen auf Cuticula-Scheiben, die auf Agarblöcken als Empfänger ausgelegt worden waren, ausgebracht. Die Wirkung auf den Chlortoluron-Transfer durch die Cuticula hing von der Ethoxylierung des Zusatzstoffes ab. In allen Serien wurde der Transfer durch Zusatzstoffe mit niedrigem Gehalt an Ethyloxiden (EO) erheblich gesteigert (3 bis 6 EO). Diese Wirkung trat 24 h nach der Applikation der Tröpfchen ein und nahm dann mit der Zeit zu. Mit dem Anstieg der Ethoxylierungszahl nahm die Wirkung ab, und Zusatzstoffe mit einer langen Ethylenoxidkette (OP16, NP20, NP40 und AA20) waren wirkungslos. Die Konzentration des OP5-Zusatzstoffes hatte großen Einfluß auf den Chlortolurontransfer; die Penetration war versiebenfacht, wenn die OP5-Konzentration von 0,01 auf 10 g l?1 angehoben wurde. Die Diffusion der Octylphenole [3H]OP5 und [3H]OP16 wurde während des Chlortolurontransfers gemessen; die Diffusionsrate war ähnlich, aber von OP5 wurde ein größerer Anteil in der Cuticula zuückgehalten. Die Wirkung der Zusatzstoffe auf das Cuticularwachs wurde calorimetrisch untersucht, und es zeigte sich, daß das Wachs in Gegenwart der Nonylphenole NP9 und NP4 bei niedriger Temperatur zu schmelzen beginnt. Die Fusionsenthalpie lag bei -30 J g?1  相似文献   

11.
Cinidon-ethyl (BAS 615H) is a new herbicide of isoindoldione structure which selectively controls a wide spectrum of broadleaf weeds in cereals. The uptake, translocation, metabolism and mode of action of cinidon-ethyl were investigated in Galium aparine L, Solanum nigrum L and the tolerant crop species wheat (Triticum aestivum L). When plants at the second-leaf stage were foliarly treated with cinidon-ethyl equivalent to a field rate of 50 g ha−1 for 48 h, the light requirement for phytotoxicity and the symptoms of plant damage in the weed species, including rapid chlorophyll bleaching, desiccation and necrosis of the green tissues, were identical to those of inhibitors of porphyrin synthesis, such as acifluorfen-methyl. The selectivity of cinidon-ethyl between wheat and the weed species has been quantified as approximately 500-fold. Cinidon-ethyl strongly inhibited protoporphyrinogen oxidase (Protox) activity in vitro, with I50 values of approximately 1 nM for the enzyme isolated from the weed species and from wheat. However, subsequent effects of herbicide action, with accumulation of protoporphyrin IX, light-dependent formation of 1-aminocyclopropane-1-carboxylic acid-derived ethylene, ethane evolution and desiccation of the green tissue, were induced by cinidon-ethyl only in the weed species. After foliar application of [14C] cinidon-ethyl, the herbicide, due to its lipophilic nature, was rapidly adsorbed by the epicuticular wax layer of the leaf surface before it penetrated into the leaf tissue more slowly. No significant differences between foliar and root absorption and translocation of the herbicide by S nigrum, G aparine and wheat were found. After foliar or root application of [14C]- cinidon-ethyl, translocation of 14C into untreated plant parts was minimal, as demonstrated by combustion analysis and autoradiography. Metabolism of [14C]cinidon-ethyl via its E-isomer and acid to further metabolites was more rapid in wheat than in S nigrum and G aparine. After 32 h of foliar treatment with 50 g ha−1 of the [14C]-herbicide, approximately 47%, 36%, and 12% of the absorbed radioactivity, respectively, were found as unchanged parent or its biologically low active E-isomer and acid in the leaf tissue of G aparine, S nigrum and wheat. In conclusion, cinidon-ethyl is a Protox-inhibiting, peroxidizing herbicide which is effective through contact action in the green tissue of sensitive weed species. It is suggested that a more rapid metabolism, coupled with moderate leaf absorption, contribute to the tolerance of wheat to cinidon-ethyl. © 1999 Society of Chemical Industry  相似文献   

12.
Intact mitochondria, isolated from red coxal muscle of the American cockroach (Periplaneta americana L.), were incubated in the presence of 1,1,1-trichloro-2,2-bis(4-chloro[14C]phenyl)ethane ([14C]DDT) to isolate a suspected binding site for DDT in the membrane sector of the mitochondrial ATPase. The requirements for the binding of DDT were compared with those for the binding of dicyclohexyl[14C]carbodi-imide([14C]DCCD), a potent inhibitory probe of mitochondrial ATPase activity. [14C]DDT appeared to bind to a proteolipid of the membrane sector, which also binds [14C]DCCD. Exchange experiments, with [14C]DCCD, [14C]DDT and unlabelled DDT at different concentrations, indicated that DDT and DCCD may be acting on a similar protein. This protein may act as the energy transducing protonophore required for the synthesis and hydrolysis of ATP in coupled mitochondria. Inhibition of mitochondrial ATPase activity may be a consequence of DDT and DCCD binding to this proteolipid protonophore, resulting in the disruption of energy transduction in muscle and nerve.  相似文献   

13.
Composition-concentration relationships between a series of C13/C14 polyoxyethylene primary alcohol (AE) surfactants and the foliar uptake enhancement of five model neutral organic compounds were examined in factorially designed experiments on wheat (Triticum aestivum L.) and field bean (Vicia faba L.) plants grown under controlled environment conditions. Model compounds were applied to leaves as c.0.2-μl droplets of 0.5 g litre?1 solutions in aqueous acetone in the absence or presence of surfactants at 0.2, 1 and 5g litre?1. Uptake of the highly water-soluble compound, methylglucose (log octanol-water partition coefficient (P) = - 3.0) was best enhanced by surfactants with high E (ethylene oxide) contents (AE15, AE20), whereas those of the lipophilic compounds, WL110547 (log P = 3.5) and permethrin (log P = 6.5), were increased more by surfactants of lower E contents, especially AE6. However, there was little difference between AE6, AE11, AE15 and AE20 in their ability to promote uptake of the two model compounds of intermediate polarity, phenylurea (log P = 0.8) and cyanazine (log P = 2.1). Absolute amounts of compound uptake were also influenced strongly by both surfactant concentration and plant species. Greatest amounts of uptake enhancement were often observed at high surfactant concentration (5 g litre?1) and on the waxy wheat leaves compared with the less waxy field bean leaves. The latter needed higher surfactant thresholds to produce significant improvements in uptake. Data from our experiments were used to construct a simple response surface model relating uptake enhancement to the E content of the surfactant added and to the physicochemical properties of the compound to be taken up. Qualitative predictions from this model might be useful in rationalising the design of agrochemical formulations.  相似文献   

14.
The effect of the monooxygenase inhibitor, 1-aminobenzotriazole (ABT) on isoproturon phytotoxicity and metabolism was studied in resistant (R) and susceptible (S) biotypes of Phalaris minor and in wheat (Triticum aestivum). Addition of ABT (2·5, 5 and 10 mg litre-1) to isoproturon (0·25, 0·5, 1, 2 and 4 mg litre-1) in the nutrient solution significantly enhanced the phytotoxicity of isoproturon against the R biotype. Isoproturon at 0·25 mg litre-1 reduced the dry weight (DW) of the S biotype by 77%, whereas the R biotype required 4·0 mg litre-1 for similar reduction. Addition of 10 mg litre-1 of ABT to the 0·25 mg litre-1 isoproturon caused 71 and 82% reduction in DW of R and S biotypes, respectively. Wheat was more sensitive to the mixture of isoproturon and ABT than the R biotype of P. minor. Reduced concentrations of ABT in the mixture from 10 to 2·5 mg litre-1 increased the DW of the R biotype more than that of the S biotype. The R biotype metabolised [14C]isoproturon at a faster rate than the S biotype. ABT (5 mg litre-1) inhibited the degradation of [14C]isoproturon in both biotypes of P. minor and in wheat. In the presence of ABT, about half of the applied [14C]isoproturon remained as parent herbicide in all the three species after two days. The metabolites were similar in the R and S biotypes and wheat as determined by co-chromatography with reference standards and mass spectroscopy (MS). ABT inhibited the appearance of the hydroxy and monomethyl metabolites and their conjugates in all the test plants. These results suggest that the activity of the enzymes responsible for the degradation of isoproturon is greater in the R than in the S biotype of P. minor, resulting in its rapid detoxification. Incorporation of the monooxygenase inhibitor ABT into the nutrient solution greatly inhibited the degradation of [14C]isoproturon in the R biotype and increased its phytotoxicity. Both hydroxylation and N-dealkylation reactions were found to be sensitive to ABT; inhibition of hydroxylation was greater than that of demethylation. Since ABT could not completely suppress isoproturon degradation, it is possible that more than one monooxygenase is involved. © 1998 SCI  相似文献   

15.
A modified leaf disc buoyancy procedure for the detection of photosynthesis-inhibiting residues in water is described. The modifications proposed, mainly the presence of sodium hydrogen carbonate in the infiltration solution, increased the sensitivity of the method and reduced the time required. The substituted urea and 1,3,5-triazine herbicides diuron, linuron, monuron, atrazine, ametryn and atraton were detected below 0.7 mg litre?1 using cucumber (Cucumis sativus L., cv. ‘Dalia’) leaf discs. A concentration as low as 0.09 mg diuron litre?1 could be detected. Although bean (Phaseolus vulgaris L., cv. ‘Bulgarian’) leaf tissue was less sensitive in this bioassay than cucumber, 0.3 mg diuron litre?1 could still be detected. The test, being very rapid (less than 30 min per determination) and relatively sensitive, could be used for the detection of photosynthesis inhibitors in recycled water used for irrigation.  相似文献   

16.
The effect of different adjuvants on the foliar uptake of difenzoquat methyl sulfate and sodium 2,4-D was studied in wild oat and field bean plants growing under controlled environmental conditions. The 14C-herbicides were applied to leaves as c. 0–2-μl droplets, usually containing 0.5 g 1?1 active ingredient, plus adjuvants in the range 0.05–5 g 1?1. The addition of non-ionic polyoxyethylene surfactants to solutions of both herbicides could induce considerable foliar uptake. Aliphatic C13C13 alcohol surfactants generally improved uptake more than nonylphenol surfactants when used at equivalent concentrations and ethylene oxide (EO) contents. The surfactant threshold for enhancement of difenzoquat uptake in wild oat was very low (0.05 g 1?1), whilst that in field bean was much higher (>0.5 g 1?1). For 2,4-D, surfactants at >0–5 g 1?1 were needed to produce substantial increases in its uptake into both species. Although surfactants of low EO content (5–6) were less efficient at promoting difenzoquat uptake than those of higher EO content (10–20), particularly in wild oat, there was little dependence on surfactant EO content for enhancement of 2,4-D uptake. Adjuvants with humectant properties also promoted penetration of difenzoquat, but less so than alcohol or nonylphenol surfactants. For formulations of both 14C-herbicides translocation was directly related to the quantity of radiolabel that had penetrated the leaf tissue. Effets de la formulation avec différents adjuvants sur l'absorption foliaire du difenzoquat et du 2,4-D: modeles experimentaux sur la folle avoine et le haricot L'influence de differents adjuvants sur l'absorption foliaire du difenzoquat methyl sulfate et du 2,4 D sodium a eétéétudiée chez la folle avoine et le haricot, cultivés sous des conditions environnementales contrôlées. Les herbicides marquees au 14C ont ete appliquées aux feuilles sous forme de gouttelettes de 0,2 μl contenant 0,5 g 1?1 de matière active, avec en plus des adjuvants de 0,05 à 5 g ?1. L'adjonction de surfactants polyoxyethylénes non ioniques aux solutions des deux herbicides pourrait induire un absorption foliaire importante. Les surfactants d'alcools aliphatiques C13/C15 ont généralement augmenté la pénétration mieux que les surfactants de type nonylphénol utilises à une concentration équivalente et que les oxydes d'éthylènes (EO). Le seuil de surfactant pour l'amélioration de l'absorption de difenzoquat sur folle avoine était très bas (0,05 g 1?1) tandis que sur haricot, il était beaucoup plus éievé (> 0,5 g 1?1). Pour le 2,4 D, des surfactants à une dose de >0,5 g 1?1 sont nécessaires pour produire une amelioration de son absorption chez les deux espéces. Bien que les surfactants à faible teneur en EO (5–6) fussent moins efficace pour favoriser l'absorption du difenzoquat que ceux a forte teneur (10–20), spécialement pour la folle avoine, il y avait une petite dépendance sur la teneur en EO pour l'amélioration de l'absorption du 2,4 D. Les adjuvants avec des propriétés d'humectation ont favorisé la pénétration du difenzoquat, mais moins que les surfactants alcool ou nonylphenol. Pour les formulations des deux herbicides marqués au 14C, le transport était directement reliéà la quantité de molécule marquée ayant pénétrée dans le tissu foliaire. Wirkung verschiedener Netzmittel auf die Blattaufnahme von Difenzoquat und 2,4-D am Beispiel von Flug-Hafer und Ackerbohne Der Einfluß verschiedener Zusatzstoffe auf die Blattaufnahme von Difenzoquat und 2,4-D-Na- Salz wurde an Flug-Hafer- und Ackerbohnen-Pflanzen unter kontroUierten Bedingungen untersucht. Die 14C-Herbizide wurden auf die Blatter mit etwa 0,2 μl großen Tröpfchen einer Lösung mit 0,5 g 1?1 AS und 0,05 bis 5 g 1?1 des Zusatzstoffs ausgebracht. Durch Zugabe von nichtionischen Polyoxyethylen-Netzmittein zu den Lösungen der beiden Herbizide konnte die Blattaufnahme erheblich gesteigert werden. Aliphatische C13C15-Alkohol-Netzmittel förderten die Aufnahme mehr als Nonylphenol-Netzmittel, wenn sie mit equivalenten Konzentrationen und Ethylenoxid-(EO)Gehalten ausgebracht wurden. Die Schwelle für die Steigerung der Difenzoquat-Aufnahme durch Netzmittel lag bei Flug-Hafer sehr niedrig (0,05 g 1?1), bei der Ackerbohne vielhöher (>0,5 g 1?1). Bei 2,4-D wurden bei beiden Arten zur deutlichen Förderung der Aufnahme Netzmittelkonzentrationen von >0,5 g 1?1 benötigt. Obwohl Netzmittel mit niedrigem EO-Gehalt (5–6) die Difenzoquat-Aufnahme weniger förderten als solche mit höherem Gehalt (10–20). besonders bei Flug-Hafer, ergab sich für die Förderung der 2,4-D-Aufnahme kaum eine Abhängigkeit vom EO-Gehalt des Netzmittels. Additive mit feuchtigkeitshaltenden Eigenschaften förderten auch die Aufnahme von Difenzoquat, aber weniger als alkoholische oder nonylphenolische Netzmittel. Die Translokation der Mischungen der beiden 14C-Herbizide stand in direktem Verhäitnis zur Radioaktivitätsmenge, die in das Blattgewebe aufgenommen wurde.  相似文献   

17.
Enzyme immunoassay (EIA) has been tested for the detection of atrazine in soil and water. EIA kits and atrazine-fortified samples were received from the International Atomic Energy Agency. Atrazine concentrations of about 0·01 μg litre-1 could be detected and the central detection point was found at about 0·15 μg litre-1 which is a reasonably sensitive region for atrazine. A validation study with spiked local water samples yielded acceptable results. No treatment was required for water samples. Extraction of atrazine from soil was done by simple shaking with methanol without any clean-up steps. Detection limits of 1×10-2 μg litre-1 for water and 5×10-3 μg kg-1 for soil were achieved. © 1998 SCI.  相似文献   

18.
The mode of action of DDT and pyrethroids was investigated in the house fly, Musca domestica L, using drug:receptor binding techniques. Both in vivo and in vitro binding studies demonstrated the existence of membrane receptors which bind specifically to [14C]DDT and [14C]cis-permethrin. The receptors show properties to be expected of a critical target site of these insecticides. These include negative temperature correlation with binding, relatively nonsensitivity to DDE, and sensitivity to Ca2+. The receptor sites are readily saturated at 45–90 nM [14C]DDT and have an apparent disassociation constant (Kd) of 12.2 nM. The maximum number of binding sites was estimated to be 17 pmol DDT/mg membrane protein (0.34 pmol/house fly head). Competition studies showed DDT, cis-permethrin, and cypermethrin bind to the same receptor but not at precisely the same site. The addition of Ca2+ to the incubation buffer significantly inhibited the binding of both [14C]DDT and [14C]cis-permethrin, suggesting the receptor binding is Ca2+ sensitive and may have a role in ion conductance.  相似文献   

19.
Among 15 soils with different cropping practices, seven which had an history of repeated atrazine applications showed accelerated degradation of this herbicide. By contrast, grassland or agricultural soils with no recorded atrazine application, at least for the last three years, had a low degradation potential. No direct relation was found between the rate of atrazine mineralisation and the size of the microbial biomass. In adapted soils, the amounts of extractable residues were lowered and the very high percentages of radioactivity from [ring-14C]atrazine recovered as [14C]carbon dioxide demonstrated that N-dealkylation and deamidation were the only processes for micro-organisms to derive carbon and energy for heterotrophic growth. Kinetics of microbial 14C accumulation revealed that atrazine ring carbon could be incorporated by direct oxidative condensation with structural components of the bacterial or fungal cell whereas side-chain carbon was preferentially used for biosynthesis of new protoplasmic cell material, as confirmed by the high turnover rate of radiolabelled microbial components. From the determination of the Michaelis–Menten parameters, Vm and Km in the presence of different selective biocides, it was possible to conclude that fungi were probably less active in atrazine degradation than bacteria and that over years the microbial atrazine-degrading community showed an increased efficiency. © 1999 Society of Chemical Industry  相似文献   

20.
E. EBERT 《Weed Research》1982,22(6):305-311
The grass weed herbicide metolachlor (2-chloro-N-[2-ethyl-6-methylphenyl]-N-[2-methoxy-1-methylethyl]acetamide) which is especially effective against wild millets, inhibits the formation of epicuticular waxes on sorghum leaves. The metolachlor protectant CGA 43089 [α - (cyanomethoximino) - benzacetonitrile] prevents the depletion of the waxes on the leaves of metolachlor-treated sorghum plants, as demonstrated by scanning electron microscopy. This alteration of the plant surface polymers also changes their permeability to the herbicide. 14C-metolachlor uptake into isolated coleoptiles and first leaves of sorghum which had been pretreated with the herbicide was increased. Incubation with added protectant reduced the uptake of 14C-metolachlor. It is postulated that the modifications caused by metolachlor and its protectant to sorghum surface structures influence the action of the herbicide in two ways:
  • 1 The selectivity observed against sorghum and millet grasses could occur because of an increased uptake of metolachlor through cuticles which are particularly sensitive to the structural changes caused by the herbicide, since the composition of the plant waxes is very species-specific.
  • 2 The loss of cuticular integrity is prevented by the protectant CGA 43089, which greatly reduces penetration of metolachlor.
  相似文献   

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