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1.
Control ofSclerotinia sclerotiorum in muskmelons was obtained by a single soil drench with benomyl. The material was found in the apical parts of the plant and in the soil until the end of the growing season. Benomyl [methyl l-(butylcarbamoyl)-2-benzi-midazolecarbamate] and thiophanate methyl-NF 44 [1.2- bis (3 methoxycarbonyl-2-thioureido) benzene], applied to seedbeds, were taken up by and then persisted in tomato, pepper and eggplant for approximately 8 weeks after application. Thiophanate-NF 35 [1.2-bis (ethoxycarbonyl-2-thioureido) benzene] could be detected only in the bottom leaves of pepper and eggplant, for up to 4 weeks after application.  相似文献   

2.
Vetiver (Vetiveria zizanioides Nash) cells derived from an inflorescence were cultured in a modified N6 liquid medium supplemented with 10 µm 2,4‐D and 10 mm proline. Exponentially growing cell suspensions were subcultured with a selection medium containing glufosinate (ammonium dl ‐homoalanin‐4‐yl(methyl)phosphinate). The glufosinate‐resistant cells which can grow in a medium containing 5 × 10?5 M glufosinate was selected by a stepwise selection, and its I50 value was determined to be 4.2 × 10?5 M. The growth of susceptible cells was inhibited by lower concentrations of glufosinate and its I50 value was 2.5 × 10?7 M. This indicated that the selected cells were 170‐fold resistant compared with the susceptible cells. Glutamine synthetase (GS) activity of the resistant cells was twice as high as that of the susceptible cells. The I50 values of glufosinate were 3.2 × 10?5 M and 9.0 × 10?7 M for GS from the resistant and susceptible cells, respectively. The accumulation of ammonia caused by GS inhibition was higher in the susceptible cells. Absorption of [3,4–14C]glufosinate was not significantly different between the resistant and susceptible cells. Both cell types did not metabolize glufosinate. These results suggest that the resistance of the selected vetiver cell suspension to glufosinate is mainly due to increased GS activity and its decreased sensitivity to the herbicide.  相似文献   

3.
Bioassays using pellets of agar, thatch-agar and turfgrass-agar were developed using benzimidazole-sensitive Penicillium expansum Link, to detect the fungicide methyl benzimidazol-2-ylcarbamate (MBC) which is the major fungitoxic degradation product of benomyl [methyl 1-(butylcarbamoyl)benzimidazol-2-ylcarbamate] in thatch and turfgrass clippings. These bioassays were used to estimate the amount of fungicide that was biologically available and hence, by subtraction from that applied, the amount that remained bound and biologically unavailable. The limit of quantitation was 0·5 mg kg−1. From 19·9% to 93·2% of the applied fungicide was bound by thatch and 46·2% to 56·9% was bound to turfgrass clippings depending on the concentrations used. In-vitro degradation studies showed that MBC had a half life of approximately 2·5 weeks at 23°C in non-sterilized thatch.  相似文献   

4.
At concentrations near 2 × 10?4M, barban, chlorpropham, and phenmedipham are inhibitors of the electron transfer in potato and mung bean mitochondria. The inhibition seems to be localized in the flavoprotein region. It affects preferentially the exogenous NADH dehydrogenation, in potato mitochondria (I50, 10?4M). Succinate dehydrogenation is less inhibited. At noninhibiting concentrations, the studied carbamates cannot uncouple the oxidative phosphorylations. Photosynthesis is completely inhibited by 2.10?7M phenmedipham, 5 × 10?5M barban, and 2 × 10?4M chlorpropham. The inhibition takes place at the PS II level. Moreover, barban and chlorpropham are uncouplers of the photophosphorylations for concentrations between 5 × 10?5 and 5 × 10?4M. The effects observed on mitochondrial respiration can also be found on respiration of Acer cultured cells. The effects on isolated chloroplast photosynthesis are also observed for slightly higher concentrations on cultured Chlorella and on pea and oat leaf fragments.  相似文献   

5.
Proctolin-induced, dose-dependent (10?8-2 × 10?6 M) contraction of the isolated foregut of Schistocerca gregaria was antagonised non-competitively by sulfotep (2 × 10?6-10?5 M). A higher dose of sulfotep (5 × 10?5 M) caused restoration of the proctolin dose-response curve to its control value. Neostigmine (10?5 M) caused non-competitive inhibition of proctolininduced tissue contraction. Increasing the dose of neostigmine to 10?4 M restored the proctolin response to control values. Sulfotep (10?5 M) and neostigmine (10?4 M) caused inhibition of acetylcholinesterase (AChE) activity in tissue homogenates obtained from guts pretreated with either drug for 20 min. The stimulatory effect of sulfotep (5 × 10?5 M) on proctolin-induced gut contraction was abolished by pretreatment of tissues with atropine (10?6 M). Under these conditions, 5 × 10?5 M sulfotep caused further antagonism of the action of proctolin. The results suggest that sulfotep is a proctolin receptor antagonist in the locust foregut. However, higher concentrations inhibit tissue AChE activity, thereby allowing endogenous acetylcholine to activate muscarinic receptors. This leads to enhanced tissue contractility which masks the antagonistic effect of sulfotep on proctolin-induced contraction.  相似文献   

6.
The formation of roots and shoots on root segments of Rubus procerus P.J. Muell was prevented by soaking the segments for 24 h in a 10?4M solution of 2,4,5-T or a 10?5M solution of picloram. Shoot numbers were significantly increased after treatment with 10?9M and 10?10M 2,4,5-T, but picloram did not cause a significant increase in shoot numbers. Measurement of the concentration of 2,4,5-T in the extracambial tissue showed that roots treated with 10?4M 2,4,5-T contained 5× 10?8 mmole 2,4,5-T per mg dry weight, and by extrapolation, roots treated with 10?9M 2,4,5-T contained 2× 10?10 mmole/mg dry weight. Action du 2,4,5-T et du piclorame sur la régénération de la ronce (Rubus procerus P.J. Muell) è partir de fragments de racines La formation de racines et de tiges è partir de fragments de racines dc Ruhus procerus P.J. Muell a été supprimée par trempage des fragmenls pendant 24 heures dans une solution a 10?4M et de 2.4,5-T, ou dans une solution 10?5M de piclorame. Le nombre de pousses s'est accru significativement après traitement avec le 2,4,5.-T è 10?9M et 10?10M, mais le piclorame n'a pas provoqué d'accroissemcnt significatif du nombre de pousses. La mesure de la concentration de 2,4,5-T dans le tissu extra-cambial a montré que les racines trailées avec du 2,4,5-T è 10?4M contenaient 5×10?8 mmole de 2.4,5-T par mg de poids sec et par extrapolation, quc les racines traitées avec du 2,4,5-T k 10?9M devaient contenir 2 × 10?12 mmole/mg de poids sec. Die Wirkiing von 2,4,5-T und Picloram auf den Wuchs der Wurzehegmenten von Bromheeren (Rubus procerus P.J. Muell). Die Bildung von Wurzeln und Sprossen aus Wurzelsegmen-ten von Ruhu.i procerus P.J. Muell wurde durch 24-stündiges Einlegen der Wurzelstücke in 10?4M 2,4,5-T bzw 10?5M Picloram verhindert. Die Anzahl neugebiideter Sprosse wurde nach Einlegen in 10?9M und 10?10M 2,4,5-T, nicht jedoch durch Picloram, signifikant erhöht. Im extracambialen Gewebe von Wurzeln, die mit 10?4M 2,4,5-T behand-elt worden waren, wurden 5×10?8mMol 2,4,5-T je mg Trockengewiclu bestimmt. Durch Extrapolation wurde ermittclt. dass mit 10?9M 2,4,5-T behandelte Wurzeln 2× 10?12mMol/mg Trockengewicht cnthielten.  相似文献   

7.
A field experiment was conducted in 1981 and 1982 to evaluate five post-emergence herbicides applied alone or following a preplant incorporated application of trifluralin for the control of Sorghum halepense (L.) Pers. in cotton (Gossypium hirsutum). One application of the methyl ester of haloxyfop [methyl 2- (4- ((3-chloro-5-trifluoromethyl)-2-pyridinyl)oxy)phenoxy)pro-panoate], trifluralin plus the ethyl ester of DPX-Y6202 [ethyl[2-[-4-(6-chloro-2-quinoxalinyl)oxy]phenoxy]propionate], the butyl ester of fluazifop and trifluralin plus haloxyfop resulted in over 90% control of S. halepense just prior to harvest in 1981 and 1982. Sorghum halepense control was similar whether the post-emergence herbicides were applied alone or following preplant incorporated trifluralin at 0.8 kg ha?1. La lutte contre Sorghum halepense (L.) Pers. en culture de cotonnier moyennant des herbicides de post-levée et la trifluraline Une expérience a été installée en plein champ en 1981 et 1982 dans le but d'évaluer cinq herbicides de post-levée, appliqués seuls ou suite à la trifluraline incorporée avant le semis, dans la lutte contre Sorghum halepense (L.) Pers. en culture de cotonnier (Gossypium hirsutum). Une seule application de l'haloxyfop ester de méthyle [méthyle 2-(4-((3-chloro-5- (trifluorométhyle)-2-pyridinyle) oxy)phénoxy)propanoate], de trifluraline + DPX-Y6202 ester d'éthyle (éthyle[2-[4-(6-chloro-2-quinoxalinyle)oxy]phénoxy)propionate), de l'ester butylique du fluazifop et de trifluraline + haloxyfop a permis en 1981 et 1982 une bonne maîtrise (90%) de S. halepense juste avant la récolte. La maîtrise de Sorghum halepenseétait semblable, que les herbicides de postlevée aient été précédés ou non d'une application de trifluraline à 0,8 kg ha?1 incorporée avant le semis. Bekämpfung von Sorghum halepense (L.) Pers. in Baumwolle mit Nachauflaufherbiziden und Trifluralin In den Jahren 1981 und 1982 wurden Feldversuche zur Bekämpfung von Sorghum halepense (L.) Pers. in Baumwolle (Gossypium hirsutum) mit fünf Nachauflaufherbiziden durchgeführt. Die Herbizide wurden allein oder nach einer vor der Baumwollsaat erfolgten Einarbeitung von Trifluralin appliziert. Eine Applikation des Methylesters von Haloxyfop [Methyl-2-(4-((3-chloro-5-(trifluormethyl)-2-pyridinyl)oxy)phenoxy)propanoat]. Von Trifluralin + Aethylester von DPX-Y 6202 [Aethyl[2-[-4-(6-chlor-2-quinoxalinyl)oxy)phenoxy)propionat], des Butylesters von Fluazifop und Trifluralin + Haloxyfop ergaben in beiden Jahren kurz vor der Ernte eine über 90 ige Kontrolle von S. halepense. Der Bekämpfungserfolg war ähnlich, gleichgültig ob die Herbizide allein oder nach der Einarbeitung von Trifluralin (0,8 kg ha?1) appliziert worden waren.  相似文献   

8.
Long-term experiments with dactyl cells of Nitella flexilis showed that the herbicide 3-(3,4-dichlorophenyl)-1,1-dimethylurea (DCMU) at a concentration of 1 × 10?5M affected not only O2 evolution in the light but also O2 uptake in the dark. The inhibition of O2 production was transitory, but dark respiration did not recover. DCMU induced the formation of giant mitochondria which disappeared before cell death. It was concluded that the algicidic effect of 1 × 10?5M DCMU on N. flexilis, but not necessarily the elongation of mitochondria, was due to the inhibition of mitochondrial respiration and not of photosynthesis.  相似文献   

9.
Following intraperitoneal administration to male mice of trichlorphone, 4 mg/animal = 160 mg/kg and butonate, 5 and 10 mg/animal = 200 and 400 mg/kg, labeled by 14C in the OCH3-groups, nucleic acids taken from different organs and urine were analyzed for [7-14C]methylguanine. The limit of detection was 2 × 10?8, calculated as 14C relative to the total dose. The maximum of 14C in 7-methylguanine was 2 × 10?7 in lung, kidney, and testicles and 3 × 10?6 in liver. The excretion rate of 7-MeG from nucleic acids is very rapid, a halflife of 2.0 hr was measured in liver from butonate and of < 24 hr was calculated in the whole body from trichlorphone, contrary to the excretion rate of 3.0–3.5 days following administration of strongly genotoxic agents. The relative amounts of [7-14C]methylguanine excreted in the urine were determined and compared with data for dichlorvos, dimethyl sulfate, and methyl methanesulfonate from the literature. Following intraperiotoneal administration, the methylating capability towards N-7 of guanine in nucleic acids is given by the ratio of about 100:10:25 for dichlorvos, butonate, and trichlorphone, respectively.  相似文献   

10.
Based on our previous finding that PIM (phenyl-imidazolyl-metyra-pon; 2-(1-imidazolyl)-2-methyl-1-phenylpropan-1-one, 1) is a strong inhibitor of ecdysone 20-monooxygenase (IC50 = 7.89 × 10?7 M) from the fleshfly, Neobellieria bullata (Parker) and has also a good toxic action in vivo against this insect, 17 imidazole and 1,2,4-triazole analogues of metyrapone were synthesized and evaluated for their action against N. bullata larvae in terms of toxicity, length of larval development, weight of the puparium as well as special symptoms, i.e. malformations of the anterior and posterior spiracles, and of the mandibles. The introduction of p-methoxy (LC50 = 49 mg kg?1 in diet) or p-chloro (LC50 = 97 mg kg?1) substituents on the benzene ring of PIM resulted in a significant increase in toxicity compared to that of metyrapone (LC50 = 561 mg kg?1) and PIM (LC50 = 148 mg kg?1). The hybridization state of the carbon atom adjacent to the benzene ring was not an important factor for toxicity because the acetoxy derivative ( 13 ) was almost as toxic as PIM. At least one methyl group was required on the carbon atom adjacent to the azole ring to maintain activity, while an ethyl group ( 4 ) enhanced the toxic effect. At the applied doses some compounds including metyrapone itself, extended the duration of the larval development. Only metyrapone and PIM decreased the puparium weight. Several derivatives induced lethal malformations of mandibles as well as the anterior and posterior spiracles.  相似文献   

11.
Permethrin at concentrations as high as 10?6 had no detectable effect upon neuromuscular transmission at 20-21°C in the body-wall muscles of susceptible larvae of Lucilia sericata and susceptible and resistant (kdr) strains of larvae of Musca domestica. At the higher concentrations of 5 × 10?6M, muscle cells in all strains and species of larva were slowly depolarised, resulting in failure of neuromuscular transmission when the level of depolarisation corresponded with the peak height of the postsynaptic potentials. Multiple postsynaptic potentials were sometimes obtained in response to a single electrical stimulus to the motor axon. Neither of these effects is considered to result from interference with release of the neurotransmitter or its binding to the postsynaptic receptors. Spontaneous activity in sensory nerve fibres from susceptible larvae was increased followed by intermittent bursting and block at concentrations of permethrin as low as 10?9M at 20-21°C and 10?10 at 26°C. Resistant larvae of M. domestica were 1000 times less sensitive, needing concentrations of permethrin as high as 10?6M at 20-21°C and 10?7M at 26°C to affect sensory discharge. The results are discussed in relationship to the cause of knockdown by pyrethroid insecticides and to possible changes in the nervous system which may be brought about by the kdr resistance factor.  相似文献   

12.
R. A. CHRIST 《Weed Research》1985,25(3):193-200
The elongation rates of single attached leaves of rice (Oryza saliva L.) were recorded. The effect of pretilachlor on the elongation rates and the safening effect of CGA 123407 [4, 6-dichloro-2-phenyl-pyrimidine] were evaluated. Both chemicals were applied to the roots in a nutrient solution. Pretilachlor reduced leaf elongation in concentrations as low as 300 μg?1 (9–6 × 10?7 M) but. for combination trials with the safener, 3 mg 1?1 (9–6 × 10?6 M) was used. in combination with pretilachlor the safener prevented damage in very low concentrations. The ratio of pretilachlor to safener, 30:1, was sufficient when both chemicals were given to roots in nutrient solution, although for field work the ratio of 3:1 is recommended. The safener alone did not influence the elongation rate of rice leaves in the concentrations used. When pretilachlor was given to the roots and CGA 123407 to the shoot, some delay in the herbicidal action was recorded but even with high concentrations of the safener no continuous safening effect was achieved. CGA 123407 was also effective when given previous to the herbicide. This proved true even with a 2-day interval between safener uptake and application of the herbicide. When pretilachlor was given first, the safener effected recovery to various degrees when given 1–4 days after the herbicide application. When pretilachlor was given for a limited period of time only (1–3 days) and was subsequently removed from the nutrient solution, recovery of the plant occurred. It is speculated that the safener either helps this recovery or else competitively prevents the herbicide from occupying the sites of action or from keeping them occupied for a long period of time.  相似文献   

13.
Tepraloxydim [(EZ)‐(RS)‐2‐{1‐[(2E)‐3‐chloroallyloxyimino]propyl}‐3‐hydroxy‐5‐perhydropyran‐4‐ylcyclohex‐2‐en‐1‐one] showed high activity against annual bluegrass (Poa annua L.), which is relatively tolerant to sethoxydim [(±)‐2‐(1‐ethoxyiminobutyl)‐5‐[2‐(ethylthio)propyl]‐3‐hydroxycyclohex‐2‐en‐1‐one]. Absorption and translocation rates of tepraloxydim and sethoxydim were higher in P. annua than in Setaria faberi, but the absorption and translocation patterns of tepraloxydim in the two plants were similar to those of sethoxydim. Metabolic rates of tepraloxydim and sethoxydim in P. annua and S. faberi were found to be similar. The concentration for 50% inhibition (I50) of acetyl‐coenzyme A carboxylase (ACCase) with tepraloxydim was approximately 3 × 10?6 mol L?1 for P. annua and 7 × 10?7 mol L?1 for S. faberi. For sethoxydim, the I50 was found to be 2 × 10?6 mol L?1 with the enzyme of S. faberi, while sethoxydim showed a slight effect on ACCase from P. annua activity, even at 10?4 mol L?1. The strong inhibition of ACCase with tepraloxydim is considered to be the major factor contributing to the high herbicidal activity against P. annua. Measuring the whole plant growth response, the ratio of the tepraloxydim I50 dose of P. annua to that of S. faberi (P/S) was found to be 2.4, while the P/S ratio of sethoxydim and a tepraloxydim analog with a propyl chain at R2 were 56.3 and 73.3, respectively. The herbicidal activity against P. annua was remarkably influenced by the length of the R2 alkyl chain, while the effect on S. faberi was not affected. Acetyl‐coenzyme A carboxylase from P. annua also exhibited a higher resistance to the tepraloxydim analog with a propyl chain than to tepraloxydim. These results suggest that a binding site structure of cyclohexane‐1,3‐diones in the ACCase differs between P. annua and S. faberi.  相似文献   

14.
Several series of alkyl-substituted amino-, bromo-, chloro-, fluoro- and hydroxy-1, 4-naphthoquinones, as well as some 6-alkylaminoquinoline-5, 8-diones and 7-alkyl-6-hydroxyquinoline-5, 8-diones were prepared and tested as protectant fungicides against apple powdery mildew (caused by Podosphaera leucotricha). While most of the compounds did not reduce infection when applied at 10?3M, several 3-alkyl-2-bromo-and 3-alkyl-2-chloro-1, naphthoquinones were found to have ED50 values below 50 × 10?5M.  相似文献   

15.
Buthidazole (3-[5-(1,1-dimethylethyl)-1,3.4-thiadiazol-2-yl]-4-hydroxy-l-methyl-2-imidazolidinone) at concentrations of 10?6-10?4M did not affect germination of corn (Zea mays L.,‘Pioneer 3780’), redroot pigweed (Amaranlhus retroflexus L.), alfalfa (Medicago saliva L., ‘Vernal’), and quackgrass (Agropyron repens(L.) Beauv.) seeds. Stressing the seeds obtained from mature corn plants treated either pre-emergence or pre- plant incorporated with buthidazole at several rates by accelerated ageing and cold treatments further indicated that this herbicide did not affect germination. Total photosynthesis and dark respiration of corn plants 12 days after pre-emergence application and of redroot pigweed, alfalfa, and quackgrass plants after postemergence application of buthidazole at several rates were measured with an infrared CO2 analyser. The results suggested that buthidazole was a rapid inhibitor of photosynthesis of the sensitive redroot pigweed and quackgrass plants, with less effect on corn and alfalfa. Buthidazole did not affect respiration of the examined species except for a transitory increase in corn and alfalfa 12 days after pre-emergence or 4 h after postemergence treatment with buthidazole at 0.56 or 1.12 and 2.24 kg/ha, respectively. A long-term inhibition of quackgrass respiration 96 h after treatment with buthidazole at 1.12 and 224 kg/ha was also evident.  相似文献   

16.
N-Arylcarbamoylpyrazolines with various substituents at the para position of the carbamoyl benzene ring inhibited ATP-dependent Ca2+-uptake in synaptosomes prepared from the rat brain. The activity of these compounds was evaluated as log(1/I50), the reciprocal logarithm of half inhibitory concentration, I50 (m ), from the concentration–response curve for the inhibition of Ca2+-uptake. Among the compounds tested, methyl 3-(4-chlorophenyl)-4-methyl-1-[N-(4-trifluoromethylphenyl)carbamoyl]-2-pyrazoline-4-carboxylate was the most potent, the I50 value of which as 9·12×10−7 m . Variations in the activity in terms of log(1/I50) were quantitatively analysed using a substituent parameter, showing that the higher the electron-withdrawing effect of the substituent, the higher was the activity. The substituent effects were similar to those on insecticidal activity against the Americal cockroach. The higher the inhibitory activity against Ca2+ uptake, the higher seemed to be the insecticidal activity. Methyl(4S) - 3 - (4 - chlorophenyl) - 4 - methyl - 1 - [N - (4 - chlorophenyl)carbamoyl] - 2 - pyrazoline -4-carboxylate had higher inhibitory activity against Ca2+-uptake and higher in-secticidal activity than the R-isomer, but the difference was greater in theCa2+-uptake system.  相似文献   

17.
Excised shoots from apple trees and cell suspension cultures were used as model systems to study the metabolism of [3,5-14C]amitrole in Malus domestica Borkh. Significant differences in the metabolism of the compound applied were observed with excised shoots, cultured cells and whole apple trees. The major metabolite in excised shoots was aminotriazolylalanine which occurred both in the free form and as conjugates. The major metabolite from whole plants. triazolylalanine, was detected in shoots in minor amounts only. In cell suspension cultures, the type of metabolism strongly depended on the concentration of amitrole when initially applied. At 10 ?3 m or lower, mainly aminotriazolylalanine was formed. Depending on the concentration of the active ingredient, this metabolite predominantly occurred in free form or as glycosides. At concentrations above 5 × 10?4 M a new metabolite, 3,5-dihydroxytriazole, was detected which was the only metabolite found at 5 × 10?3M. Significant amounts of nonmetabolized amitrole remained in the medium.  相似文献   

18.
BACKGROUND: Testing the compatibility of chemical pesticides and fungal biocontrol agents is necessary if these two agents are to be applied together in the integrated management of plant pests and diseases. In this study, the fungicides azoxystrobin (a strobilurin) and flutriafol (a triazole) were tested in vitro for their effects on germination of conidia and mycelial growth of Beauveria bassiana (Bals.) Vuill. and in bioassay for their effect on fungal activity against Tetranychus urticae Koch. The fungicides were tested at three different concentrations [recommended rate for field use (1 × X) and the dilutions 10?1× X and 10?2× X]. RESULTS: Flutriafol inhibited growth of mycelia and germination of the fungal conidia at all concentrations tested in vitro, and also reduced the efficacy of B. bassiana in bioassays against mites. The inhibitive effect of azoxystrobin in vitro varied with the concentration applied. A significant effect was observed at 1 × X and 10?1× X concentrations on both the germination of conidia and mycelia growth. At 10?2× X concentration, azoxystrobin showed little effect on B. bassiana. However, when this fungicide was tested in bioassays, none of the concentrations reduced B. bassiana activity against mites. CONCLUSION: Azoxystrobin was most compatible with B. bassiana, while flutriafol was the most harmful. Further studies are required to confirm the negative effect of flutriafol on B. bassiana activity. Copyright © 2010 Society of Chemical Industry  相似文献   

19.
The binding behavior of mercuric chloride (HgCl2), phenylmercuric acetate (PMA), and ethylmercuric chloride (EMC) to the spinach chloroplasts in relation to the inhibition of the Hill reaction was studied at pH 6.8 and 7.8 using 203Hg labeled compounds. The pH of the reaction medium did not influence the amount of mercury binding of the chloroplast at various mercurial concentrations, but it altered the inhibition curve of the Hill reaction. Between 0–1 × 10?5M the binding of Hg2+ and EMC were similar and increased linearly with the concentration, while the binding of PMA was similar to the binding of Hg2+ only at a concentration below 4 × 10?6M and was less when the concentration was above 4 × 10?6M. However, the inhibition of the Hill reaction by these mercury compounds was quite different; at pH 7.8, the I50 values for Hg2+, PMA, and EMC were 5 × 10?6, 2.5 × 10?6, and 2.5 × 10?6M, respectively, while at pH 6.8, these values were 4 × 10?6, 4 × 10?5, and 2 × 10?4M, respectively. The differential block of electron flow by the mercury compounds at pH 6.8 and 7.8 was further confirmed by electron spin resonance study.  相似文献   

20.
The hydrolysis of [14C] fenpropathrin ( I ) [(RS)-α-cyano-3-phenoxybenzyl 2,2,3,3-tetramethylcyclopropanecarboxylate] was studied in buffer solutions at pH 1.9–10.4, and in natural river and sea water at 25, 40, 55 and 65°C under laboratory conditions. The hydrolysis of I proceeded predominantly through neutral (pH independent) and base-catalysed processes in the regions below pH 3.9 and above pH 7.0, respectively, whereas both reactions occurred between pH 3.9 and 7.0. The rates of hydrolysis of I in buffer solutions were similar to those in one sample of river and one sample of sea water. If this obtains generally, it may be expected that the half-life of I in natural waters, normally within the range pH 5–9, will range from 1.54 to 1080 days at 40°C, 11.3 to 8520 days at 25°C and, by extrapolation of the data obtained in buffer solutions, 106 to 83 000 days at 10°C. The rate constants for hydrolysis of I in aqueous media can be expressed by: Where log kN = 9.60–(5.56 × 103 T?1) and log kB = 7.32–(2.56 × 103 T?1). The calculated rate constants were in good accord with the observed values in buffer solutions. Cleavage of the ester linkage was more rapid than hydration of the cyano group at any pH and temperature tested.  相似文献   

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