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.     

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.     

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.     

Demonstrating formation of potentially persistent transformation products from the herbicides bromoxynil and ioxynil using liquid chromatography-tandem mass spectrometry (LC-MS/MS)

It is shown that potentially persistent transformation products can be formed from the herbicides bromoxynil (3,5-dibromo-4-hydroxybenzonitrile) and ioxynil (3,5-diiodo-4-hydroxybenzonitrile), and possible leaching to groundwater is discussed. A similar process to the formation of BAM (2,6-dichlorobenzamide) from the herbicide dichlobenil (2,6-dichlorobenzonitrile) can be anticipated as bromoxynil and ioxynil are analogues of dichlobenil and they are degraded by the enzymes nitrilase, nitrile hydratase and amidase. A biodegradation study using cultured Variovorax sp. DSM 11402, a species commonly found in soil, demonstrated that ioxynil and bromoxynil were fully transformed into their corresponding amides in 2-5 days. These amides were not further degraded within 18 days, and formation of other degradation products was not observed. These results are in agreement with biodegradation experiments with dichlobenil. In soil, dichlobenil is transformed into its only observed degradation product BAM, which is persistent and mobile, and has been found in 19% of 5000 samples of Danish groundwater. Variovorax sp. is known to degrade the non-halogenated analogue benzamide, suggesting that degradation of the three amides may be hindered by the halogenated substituents (meta-Br; meta-I; ortho-Cl). This hypothesis is supported by QSAR modelling of fundamental properties. Using a new optimised liquid chromatography-tandem mass spectrometry (LC-MS/MS) method, the sorption and desorption properties of bromoxynil and ioxynil were characterised in sandy topsoil at four concentration levels. The estimated sorption coefficient K(d) was 1.4 L kg(-1) for bromoxynil and 5.4 L kg(-1) for ioxynil, indicating weak to moderate sorption to topsoil. Desorption of the herbicides showed that they were strongly and irreversible bound to the soil (K(des) > K(d)). The amount of herbicide desorbed depended on the initial concentration level. At low levels, K(des) values were higher, indicating stronger binding than at higher levels. The isocratic LC-MS/MS method developed for simultaneous detection of bromoxynil, ioxynil and their main degradation products is described. Using negative electrospray ionisation (ESI-), the detection limits were 0.4-1.0 microg L(-1), with relative standard deviations of 4-10% (n = 10) using direct injection without clean-up steps. The standard curves showed linearity in the range 5-100 microg L(-1) with r(2) > 0.992.     

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.     

溴苯腈与精喹禾灵混用对亚麻的安全性及控草效果

为筛选防控亚麻田杂草的安全高效药剂,采用喷雾法,通过室内生物测定和田间试验测定了溴苯腈和精喹禾灵混用对亚麻的安全性和对亚麻田杂草的防效,并研究了除草剂混用对亚麻产量的影响。结果表明:在室内条件下,溴苯腈与精喹禾灵按有效成分含量375~450 g/hm2混用,施药后21 d,亚麻无药害症状,当用量增至675 g/hm2时,亚麻苗失绿症状明显,有烧叶现象,呈中度药害中毒症状;二者混用对稗草Echinochloa crusgalli和反枝苋Amaranthus retroflexus的选择性系数均为1.42,高于对照药剂2甲4氯钠 (其对稗草和反枝苋的选择性系数分别为0.53和0.85),表明该混用药剂在亚麻田应用存在潜在的药害风险,在保证除草效果的前提下,须严格控制其用量;该混用药剂以有效成分371.25 g/hm2在田间应用时,药后35 d对亚麻田杂草的株防效和鲜重防效均达85%以上,亚麻株高平均增加42.33 cm,高于对照药剂溴苯腈 (株高增加40.93 cm)、精喹禾灵 (株高增加41.80 cm) 和空白对照 (株高增加39.07 cm),且平均鲜重比单用溴苯腈和精喹禾灵分别提高2.7%和4.6%,比空白对照提高8.3%。表明溴苯腈与精喹禾灵混用可以用于防治亚麻田禾本科和阔叶杂草,但为了防止药害的发生,应严格控制用量,并使用防护罩喷头进行定向喷雾。     

Oral administrations of methamidophos and TOCP have different effects on in vitro protein phosphorylation levels from subcellular fractions of hen brain

The effects of methamidophos and tri-o-cresyl phosphate (TOCP) on the endogenous phosphorylation of specific brain proteins were studied in Beijing white laying hens during the early stage of delayed neurotoxicity. Phosphorylation of mitochondrial and synaptosomal proteins was assayed in vitro by using [γ-³²P]ATP as phosphate donor. Tri-o-cresyl phosphate (TOCP) administration enhanced the phosphorylation of synaptosomal proteins with molecular weight of 40 and 55 kDa by as much as 36% and 65%, respectively, and decreased the phosphorylation of mitochondrial protein (35 kDa) by 33%. A single dose of methamidophos enhanced the phosphorylation of 32-kDa synaptosomal protein by 44%; however, it had no effect on brain mitochondrial proteins. The activity of neuropathy target esterase (NTE) in dosed hens’ brain and spinal cord was assayed for the effects of methamidophos and TOCP. These results showed that methamidophos inhibited brain NTE by 41% compared with that of control after 7-day exposure, while TOCP inhibited brain NTE by 66%. Moreover, NTE activity from spinal cord in treated hens also exhibited a similar trend of activity inhibition. Together, these results suggested that methamidophos and TOCP induced changes of protein phosphorylation level from hen brain and resulted in different kinds of neurotoxicity.     

Analytical method for residues of bromoxynil octanoate and bromoxynil in soil

A method is described for the analysis of bromoxynil and its octanoate in soil. The sample is extracted with ammoniacal methanol which, on standing, converts any octanoate present to bromoxynil. Diazomethane converts this to bromoxynil methyl ether which is estimated by g.l.c. Additional clean-up may be effected by t.l.c. With a 40 g sample the method can detect 0.05 mg/kg. Recoveries are better than 80 % down to 0.1 mg/kg and about 55 % at the limit of detection (0.05 mg/kg).     

苯醚甲环唑亚急性经口暴露对大鼠卵巢功能的影响

苯醚甲环唑应用广泛，在食用农产品中存在残留超标现象，并在不孕女性人群血清和卵泡液中有检出。为探究苯醚甲环唑亚急性经口暴露后对卵巢功能的影响，本研究采用酶联免疫分析方法，测定了分别灌胃给予50、100和200 mg/(kg bw·d)剂量的苯醚甲环唑玉米油溶液后，大鼠血清中孕酮(P)和雌二醇(E2)含量的变化，并在对大鼠卵巢进行苏木精-伊红(HE)染色后，通过光学显微镜观察统计了各级卵泡的数量。结果表明：苯醚甲环唑各剂量暴露组及对照组大鼠卵巢脏器系数均无显著性差异。200 mg/(kg bw·d)高剂量暴露组大鼠血清孕酮水平显著高于对照组(P <0.01),50和100 mg/(kg bw·d)剂量暴露组则与对照组无显著性差异，但均显著低于高剂量暴露组(P <0.05)；各剂量暴露组及对照组之间血清雌二醇水平均无显著性差异。从卵泡的发育情况看，200 mg/(kg bw·d)高剂量暴露组生长卵泡的占比显著高于对照组(P <0.05),50和100 mg/(kg bw·d)剂量暴露组则与对照组无显著性差异。研究表明，200 mg/(kg bw·d)剂量的苯醚甲环唑亚急性经...     

Imidazenil,a new drug for the management of convulsions in organophosphate intoxication in rodents

The summary deals with the anti-convulsant and antilethal effects of a new benzodiazepine receptor partial agonist, imidazenil, in DFP intoxication. It has been demonstrated that imidazenil (2–5 mg kg⁻¹) significantly decreases convulsion intensity, rapidly inhibits seizure patterns in brain bioelectrical activity and significantly increases the anti-lethal efficacy of atropine plus obidoxime therapy. These effects are comparable to diazepam at 5 mg kg⁻¹. However, diazepam exhibits myorelaxant activity at therapeutic doses, which are only observed at 5–10 times the therapeutic doses of imidazenil.     

The effect of ronnel and its oxygen analog on succinate oxidation by rat brain,liver homogenates,and mitochondria

The effect of the thiophosphoroorganic insecticide ronnel and its oxygen analog on oxygen consumption by homogenates, and on succinate dehydrogenase and cytochrome oxidase activities in the mitochrondrial fractions of rat brain and liver, was investigated. A marked inhibition of blood plasma cholinesterase activity by the oxygen analog was demonstrated, but acetylcholinesterase activity was not affected. In contrast to its thiophosphoroorganic precursor, the oxygen analog caused a significant decrease in oxygen consumption by rat brain and liver homogenates and a decrease in cytochrome oxidase activity in both solubilized mitochondrial fractions. The succinate dehydrogenase activity was reduced only slightly by the oxygen analog in the brain fraction, but was marked in the liver fractions. The results suggest that the toxic activity of ronnel in vivo may be ascribed to its oxygen analog which appears as a metabolite of the former.     

Studies on the effects of herbicides on soil nitrification,II

The effects of selected herbicides have been studied on the following parameters of soil nitrification processes: the rates of nitrate and nitrite formation from ammonia in freshly perfused soils and in soils previously saturated with nitrifying organisms in an improved perfusion apparatus; the rates of oxygen consumption and of oxidation of ammonia and nitrite in washed cell suspensions of Nitrosomonas europaea and Nitrobacter winogradskii, respectively; the rates of growth of those two organisms in newly established cultures; the rates of oxygen uptake by soil enriched in nitrifying organisms; the rates of proliferation of nitrifying populations in freshly perfused soil. ID50 values were computed for all parameters and herbicides studied. On average, the most sensitive parameters were the metabolism and growth of the two organisms in pure culture, while the least sensitive were the corresponding measures in the soil environment. Similarly, herbicides fell into four distinct groups. The most toxic were the formulated octanoates of bromoxynil and ioxynil (NPH1320 and Totril, respectively); next in order of toxicity were chlorbufam, phenmedipham, formulated oxadiazon, formulated legurame, ioxynil, formulated trifluralin, and bromoxynil; low toxicity was shown by terbacil, dicamba, and tricamba, whereas asulam and the related experimental herbicide MB9555 showed activity on some parameters at the very highest concentrations only. Comparisons of soil with pure-culture parameters showed that the relative toxicities of herbicides to Nitrosomonas in culture bore little relationship to those in soil. The inhibitions of Nitrobacter proliferations in soil on the other hand were correlated with the inhibitions of growth and metabolism in pure culture. Within these overall effects, individual herbicides showed marked differential actions on various parameters. Thus, the formulated octanoates of bromoxynil and ioxynil were extremely toxic to the growth of nitrifying organisms in culture, an action probably due to an unknown formulation component. Relative to other herbicides, bromoxynil and ioxynil were more effective on nitrification processes in the soil environment. Both in culture and in the soil, Nitrobacter is more sensitive than Nitrosomonas to these four herbicides. Legurame and oxadiazon are relatively more toxic to Nitrosomonas in culture, but this differential action is not demonstrable in the soil. Dicamba, tricamba, trifluralin, and chlorbufam are more toxic to Nitrobacter than to Nitrosomonas in the soil environment. Formulated trifluralin seems to exert a stimulating action on the growth of nitrifying organisms, but only in the soil; suppression of antagonistic organisms is suggested as a possible cause. Extrapolation of these results to the field situation suggests that the only herbicide which might cause small inhibitions of nitrification at field rates is terbacil, which is disproportionately toxic at low concentrations. At rates somewhat in excess of normal, the formulated octanoates of bromoxynil and ioxynil and possibly dicamba and oxadiazon could also cause small inhibitions.     

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.     

Effect of thiamethoxam on cockroach locomotor activity is associated with its metabolite clothianidin

BACKROUND: In the present study, the effect of thiamethoxam and clothianidin on the locomotor activity of American cockroach, Periplaneta americana (L.), was evaluated. Because it has been proposed that thiamethoxam is metabolised to clothianidin, high‐performance liquid chromatography coupled with mass spectrometry was used to evaluate the amount of clothianidin on thiamethoxam‐treated cockroaches. RESULTS: One hour after neonicotinoid treatment, the time spent in the open‐field‐like apparatus significantly increased, suggesting a decrease in locomotor activity. The percentage of cockroaches displaying locomotor activity was significantly reduced 1 h after haemolymph application of 1 nmol g^?1 neonicotinoid, while no significant effect was found after topical and oral administration. However, at 24 and 48 h, all neonicotinoids were able to reduce locomotor activity, depending on their concentrations and the way they were applied. Interestingly, it was found that thiamethoxam was converted to clothianidin 1 h after application, but the amount of clothianidin did not rise proportionately to thiamethoxam, especially after oral administration. CONCLUSION: The data suggest that the effect of thiamethoxam on cockroach locomotor activity is due in part to clothianidin action because (1) thiamethoxam levels remained persistent 48 h after application and (2) the amount of clothianidin in cockroach tissues was consistent with the toxicity of thiamethoxam. Copyright © 2010 Society of Chemical Industry     

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.     

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.     

Yield losses in weed-free wheat and barley due to post-emergence herbicides

The tolerance of weed-free wheat and barley to a range of herbicides (bromoxynil, methabenzthiazuron, MCPA, bromoxynil + MCPA. linuron, prometryne, diuron, 2,4-D ester and 2,4-D amine) when applied at the crop three-leaf stage, was examined over the 5-year period 1968–72. All chemicals lowered grain yields to some extent, but the variation between chemicals was greater for wheat than for barley. In both crops, methabenzthiazuron was the safest chemical causing only small (<2·0%,) yield losses at rates up to 2·25 kg a.i./ha. At this rate of application yield losses of up to 36% were recorded for the substituted urea derivatives. Both crops had a low tolerance to 2,4-D ester and amine. Yield losses from bromoxynil, bromoxynil + MCPA and MCPA were similar, varying from 4 to 8% al 0·5 kg a.i./ha to 9–24% at 2·25 kg a.i./ha. Pertes de rendement dans le blé et l'orge provoquées, en l'absence de mauvaises herbes, par des herbicides de postlevée Pendant une période de 5 années (1968–1972) les auteurs ont examiné la résistance du béet de l'orge. Traités, en l'absence de mauvaises herbes, au stade 3 feuilles, avec une série d'herbicidcs (bromoxynil, méthabenzthiazuron, MCPA, bromoxynil-i-MCPA, linuron, prométrync. ditiron, 2,4-D ester et 2,4-D a mine). Tous ces produits ont diminué les rendements en grains dans des proportions variées, mais la variation entre produits a été plus grande pour le blé que pour l'orge. Pour les deux céréales, le méthabenzlhiazuron a été le produit le moins toxique, provotjuant seulement de faibles penes de rendement inférieurcs à 2,0%, à des doses allant jusquà 2,25 kg/m.a/ha. A cette dose d'application, des pertes de rendement allant jusquà 36% ont élé enregistrées avec des urées substituées. Les deux éréles ont manifesté uoe faible resistance au 2,4-D estr et amine. Les pertes de rendement provoquées par le bromoxynil, le bromoxynil + MCPA, et le MCPA ont été analogues, variant de 4 à 8% pour 0,5 kg/m.a./ha, jusqu’à 9 à 24% pour 2,5 kg/m.a./ha. Ertragsverluste durch Nachaufiatifherbizide in unkrautfreiem Weizen und Gerste In unkrautfreien Weizen- und Gerstebestánden wurde in fünfjáhrigen Versuthcn (1968–72) die Toleranz der beiden Arten gegenüber folgenden Herbiziden untersucht: Bromoxynil, Methabenzthiazuron, MCPA, Bromoxynil + MCPA. Linuron, Prometryn, Diuron, 2,4-D-Eister und 2,4-D-Amin- salz. Die Behandlung erfolgte jeweils im 3-Blattstadium. Alle Verbindungen erniedrigten zu einem gewissen Grad den kornertrag. Beim Weizen waren aber die Unterschiede zwischen den verschiedenen Herbiziden grösser als bei der Gerste. Methabenzthiazuron war bei Aufwandmengen bis zu 2.25 kg A.S./ha in beiden Getreidearten das sicherste Herbizid und verursachte nur geringe Ertragsdepressionen (<2%). Bei dieser Aufwandmenge wurden bei den Harn-stoffherbiziden bis zu 36% Ertragsverlust festgestellt. Gegen 2,4-D-Ester und 2,4-D-Aminsalz waren Weizen und Gerste wenig tolerant. Die Ertragsverluste durch Bromoxynil, Bromoxynil + MCPA und MCPA waren etwa gleich und betrugen 4–8% bei 0.5 kg A.S./ha bis 9–24% bei 2,25 kg A.S./ha.     

Interaction between glyphosate and various herbicides for broadleaved weed control

The effects of several herbicides for broadleaved weed control on glyphosate (n-phosphonomethyl glycine) phytotoxicity to wheat (Triticum aestivum L.), barley (Hordeum vulgare L.) and wild oats (Avena fatua L.) were studied in the greenhouse. In tank mixtures, dicamba (3,6-dichloro-o-anisic acid), 2,4-D (2,4-dichlorophenoxy-acetic acid) and bromoxynil (3,5-dibromo-4-hydroxy benzonitrile) reduced the phytotoxicity of threshold rates of glyphosate on all three species. With increasing rates of the herbicides for broadleaved weed control relative to a fixed rate of glyphosate, there was a general trend towards increased antagonism. Increasing glyphosate rates above the threshold level in mixtures containing a fixed rate of herbicides for broadleaved weed control overcame the antagonism. Both the inert and active ingredients of 2,4-D amine and ester appeared to be involved in the antagonism. There was no reduction in glyphosate phytotoxicity on the annual grasses when 2,4-D or bromoxynil were sprayed sequentially at various times in relation to glyphosate. When droplets of bromoxynil and glyphosate were placed side by side on a leaf, glyphosate phytotoxicity was not reduced, whereas when the two herbicides were mixed and applied as one droplet, considerable reduction in glyphosate phytotoxicity occurred. These results suggest that the reduction in glyphosate phytotoxicity caused by tank mixing with herbicides such as 2,4-D, bromoxynil and dicamba may be due to a physical or chemical incompatability within the tank mixture rather than to a biological interaction in the plant.     

Species differences in the in vitro inhibition of brain acetylcholinesterase and carboxylesterase by mipafox,paraoxon, and soman

Acute intraperitoneal toxicity of mipafox, paraoxon, and soman was highest in chicken, followed by rat, and lowest in frog. Species differences in organophosphorus toxicity were not related to differences in the specific activities of either acetylcholinesterase or carboxylesterase in brain. The sensitivity to inhibition of brain acetylcholinesterase in vitro by the organophosphorus compounds was closely related to the susceptibility of the species to acute organophosphorus poisoning. Both the acute toxicity and the sensitivity of brain acetylcholinesterase to inhibition in vitro by organophosphorus compounds in all the species were in the following order of increasing activity: mipafox < paraoxon < soman. The sensitivity of brain carboxylesterase to inhibition by the organophosphorus compounds were less than that of acetylcholinesterase and it could not be related to species susceptibility to acute organophosphorus toxicity. Paraoxon-insensitive phenyl valerate hydrolase in chicken brain was more sensitive to inhibition by mipafox and soman compared to rat; in chicken the sensitivity of paraoxon-insensitive phenyl valerate hydrolase to inhibition by soman was 9000 times more than that by mipafox, while in rat it was 100 times more. Frog brain had no paraoxon-insensitive phenyl valerate hydrolase activity. No evidence of age dependence was noticed in the specific activities of brain acetylcholinesterase, carboxylesterase, neurotoxic esterase, and paraoxon-insensitive phenyl valerate hydrolase or in the sensitivity of these enzymes to in vitro inhibition by organophosphorus compounds in both rats and chickens.     

杀虫安对小鼠脑组织内神经递质的影响

研究了杀虫安经灌胃给药后对小鼠脑组织内多巴胺及氨基酸含量的影响。将60只ICR (美国癌症研究所)小鼠随机分为空白对照、杀虫安低剂量(200 mg/kg bw)及高剂量(300 mg/kg bw) 3个处理组,于灌胃后出现惊厥时断头取脑,采用高效液相色谱-电化学(HPLC-ECD)检测法测定了鼠脑组织内多巴胺(DA)及其代谢产物二羟苯乙酸(DOPAC)和高香草酸(HVA)的含量,采用液相色谱-质谱联用(LC-MS/MS)法测定了氨基酸的含量。结果发现,两个剂量处理组鼠脑组织内DA及氨基酸含量与对照相比均有显著性差异。其中:DA比对照分别升高25.25%和31.93%(PPPPγ-氨基丁酸(GABA)含量比对照降低32.55% (PP<0.05)。表明杀虫安导致惊厥时伴有鼠脑内多巴胺和氨基酸含量的变化。