Photostabilization of quinalphos by crystal violet on the surface of kaolinite and palygorskite

Photochemical stability of the insecticide, quinalphos (O,O-diethyl O-quinoxalin-2-yl phosphorothioate), adsorbed on kaolinite and palygorskite was studied. In all cases considerable photostabilization was achieved in comparison with the sample of pesticide in its free form. Improvement of photostabilization was achieved when a cationic dye (crystal violet) was co-adsorbed with the quinalphos. The interactions between quinalphos and clays were studied by Fouriertransform infra-red spectroscopy. It is suggested that photostabilization is due to steric hindrance imposed by the clay surface to the isomerization step of photochemical reaction and pacification of clay surface by crystal violet.     

喹硫磷在茶叶中的残留降解

在杭州和长沙两地两年用不同剂量、不同施药方法进行的研究表明,喹硫磷在茶树鲜叶上降解速度中等,1天后的降解率平均7.15％,降解速度低于辛硫磷、马拉硫磷、敌敌畏等农药。用25％乳剂800倍液喷施后5天鲜叶中残留量低于10ppm,10天后低于1ppm,降解速率常数(K)0.47±0.06天,半衰期1.37±0.02天。降雨对喹硫磷在茶树上的降解有一定影响,尤其在施药后的近期。对成茶中在喷后不同间隔天数的残留量、含喹硫磷残留的鲜叶在加工过程中的降解率、成茶中喹硫磷残留量在泡茶时的浸出率,均进行了测定,并讨论了喷后不同间隔期鲜叶上的残留量和茶尺蠖幼虫致死剂量间的关系。建议喹硫磷在成茶中允许残留标准暂订为0.2ppm,茶叶喷施25％乳油800倍液后的安全间隔期为8—10天。     

Dissipation of quinalphos (O,O, diethyl O‐quinaxalin‐2yl phosphorothioate) residues in and/or on cauliflower (Brassica oleracea Var. Botrytis)

Abstract

A field trial was conducted to study the magnitude of quinalphos residues in and/or cauliflower (Brassica oleracea Var Botrytis. The cauliflower crop was sprayed once with quinalphos 25 e.c. at 0.25 and 0.5 kg a.i./ha 104 days after transplanting. The samples of cauliflower drawn at different time intervals were analysed colorimetrically. The initial deposits of quinalphos on cauliflower were found to be 5.79 and 9.52 ppm, an the half life values 1.61 and 2.12 days, respectively, at 0.25 and 0.5 kg a.i./ha. The waiting periods determined were 11 days at the higher and 7 days at the lower dose of quinalphos.     

Multiphase photodegradation of quinalphos

Photodegradation of the organophosphorous insecticide quinalphos (O, O-diethyl O-quinoxalin-2-yl phosphorothioate) has been studied. On exposure to natural sunlight, quinalphos was photodegraded with half-lives of 30 days in distilled water, 20–23 days in tap and rain water and ≤5 days in 2% aqueous acetone. Quinalphos underwent photoisomerisation, oxidation from P=S to the P=O group and de-esterification. Photoproducts were isolated and characterised by spectroscopic methods. When applied on soil thin-layer plates quinalphos was promptly dissipated with a half-life of ≤6 days.     

Sex attractant for the banana moth,Opogona sacchari Bojer (Lepidoptera: Tineidae): provisional identification and field evaluation

BACKGROUND: The banana moth, Opogona sacchari Bojer, is a polyphagous agricultural pest in many tropical areas of the world. The identification of an attractant for male O. sacchari could offer new methods for detection, study and control. RESULTS: A compound extracted from female O. sacchari elicited responses from antennae of male moths. This compound was identified as a 2/3,(Z)13‐octadecadienal by gas chromatography‐mass spectrometry. An analog, 2/3,(Z)13‐octadecadienol, was also detected in some extracts at roughly a 1:20 ratio (alcohol:aldehyde) but did not elicit responses from antennae of male moths. Electroantennograms of synthetic candidate dienals found the strongest responses from (Z, Z)‐2,13‐octadecadienal and (E, Z)‐2,13‐octadecadienal. In field trials, (E, Z)‐2,13‐octadecadienal attracted more male O. sacchari than (Z, Z)‐2,13‐octadecadienal. Attraction was not improved for either of these compounds when the corresponding stereoisomeric alcohol was added at ratios of 1:1, 1:10 or 1:100 (alcohol:aldehyde). Jackson sticky traps containing 250 µg lures of (E, Z)‐2,13‐octadecadienal caught as many males as did traps holding virgin females. CONCLUSION: (E, Z)‐2,13‐octadecadienal has been identified as an attractant for O. sacchari males and can be used as a monitoring lure of populations of this moth. Copyright © 2010 Society of Chemical Industry     

Interception and persistence of parathion and fenvalerate on cotton plants as a function of application method

Parathion (O,O-diethyl O-4-nitrophenyl phosphorothioate) and fenvalerate [(RS)-α-cyano-3-phenoxybenzyl (RS)-2-(4-chlorophenyl)-3-methylbutyrate] were applied by controlled droplet applicators (CDAs) and conventional hydraulic nozzles in refined soybean oil, soybean oil + water, or water, to mature cotton plants (Gossypium hirsutum L.) as ULV (ultra-low volume, < 5 litre ha^?1), VLV(very low volume, 5-50 litre ha^?1), or LV(low volume, 50–200 litre ha^?1) carrier rates. The use of CDA or soybean oil applied as ULV and VLV sprays did not produce greater deposition or persistence for either insecticide during the 49-h test period following application. In general, insecticide persistence was greatest when applied with water or soybean oil + water as LV sprays using the conventional TX8 hydraulic nozzle.     

Toxicity of some insecticides to Apanteles plutellae a parasite of the diamond back moth∗

Abstract

The susceptibility of adults and cocooned stages of Apanteles plutellae Kurdj. (Hymenoptera, Braconidae) to four synthetic pyrethroid insecticides and five other chemical insecticides was tested. The chemicals, formulated as emulsifiable concentrates, were decamethrin (0.0014%), permethrin (0.01%), fenvalerate (0.01%), cypermethrin (0.005%), dichlorvos (0.05%), monocrotophos (0.05%), endosulfan (0.05%), phosalone (0.05%) and quinalphos (0.05%). Adults were exposed for 6 h to filter paper impregnated with insecticide solution and were then transferred to untreated vials for observation. Cocoons were sprayed with the chemicals by means of a glass atomiser and held for adult emergence. The pyrethroid formulations and phosalone had little or no harmful effect on the adults and cocooned stages of A. plutellae but quinalphos was highly toxic to all stages tested. Dichlorvos, monocrotophos and endosulfan were highly toxic to adults but relatively safe for the cocooned stages.     

Activity of two pyrethroids against blackfly larvae,determined by a simple laboratory technique

A simple laboratory technique for determining the activity of two pyrethroids (5-benzyl-3-furyImethyl DL-cis, trans-chrysanthemate and 5-benzyl-3-furylmethyl D-trans-chrysanthemate) against blackfly larvae (Simulium ornatum) is described. The results showed that the pyrethroids alone or with piperonyl butpxide were of similar activity to Abate (O,O,O',O'-tetramethyl O,O'-thiodi-p-phenylene phosphor-othioate) and Dursban (O,O-diethyl O-3,5,6-trichloro-2-pyridylphosphorothioate), insecticides of known activity against blackfly larvae. However, the pyrethroids cause rapid larval detachment in running water, and may be of value in controlling these insects when used in conjunction with another insecticide.     

The degradation of (Z)- and (E)-1,3-dichloropropenes and 1,2-dichloropropane in soil

The degradation in soil of the major constituents of a 1,3-dichloropropene-1,2-dich-loropropane nematicide has been studied under laboratory and outdoor conditions. In sealed glass containers, ( Z)- and ( E)-1,3-dichloropene- 2-¹⁴C were converted in soil into the corresponding 3-chloroallyl alcohols and these alcohols were in part strongly bound to the soil. The ( Z)- and ( E)-3-chloroacrylic acids were also found as minor products. More polar products were detected and these released the chloroacrylic acids in 20–30% yield upon hydrolysis. Although the 1,3-dichloropropenes were lost by volatilisation from soil stored in open glass jars outdoors, they also underwent degradation to the same products that were detected in sealed containers. There was evidence of only slight degradation of 1,2-dichloropropane- 2-¹⁴C (4 % or less of the applied radioactivity remained unextracted from a loam soil after 5 months). When soil treated with the 1,2-dichloropropane was stored outdoors in an open glass container, less than 1 % of the original radiolabel remained in the soil after 10 days under these conditions due to volatilisation of the applied material. In a separate experiment potatoes were grown in soil 6 months after treatment with a mixture of both ( Z)- and ( E)-1,3-dichloropropene- 2-¹⁴C and 1,2-dichloropropane- 2-¹⁴C. Although 5 % of the applied radiolabel remained in the soil at potato harvest the potato tubers contained only a very small residue (0.007 mg/kg).     

Economic threshold for the management of <Emphasis Type="Italic">Plutella xylostella</Emphasis> with granulovirus in cauliflower ecosystem

Resistance to chemicals and some biological control agents by Plutella xylostella has resulted in the search for alternatives, such as P. xylostella granulovirus (PlxyGV), for the management of P. xylostella. However, use of PlxyGV would be economical only if it is applied at the right crop stage and at economic threshold levels. Hence, we evaluated the field level economic threshold for application of PlxyGV at the reproductive phase of cauliflower taking into consideration both the economic threshold model and the economic optimization model. PlxyGV was found to be very effective in management of the pest and was comparable to weekly applications of quinalphos 25EC. However, due to the higher cost of PlxyGV application than quinalphos, the cost benefit ratio with quinalphos application was much higher than the virus application. The net income from the virus application decreased both at lower thresholds—due to the higher cost of plant protection, and at higher thresholds—due to the increased damage by the pest. Based on the economic threshold model, the economic threshold for application of PlxyGV was estimated at 9–11 larvae per ten plants. Considering the net income per hectare and the cost of plant protection, it was found that at a threshold of 12–14 larvae per ten plants net income was just equal to the cost of plant protection. Based on the economic optimization model, the optimum threshold for application of PlxyGV was 15 larvae per ten plants when profits are maximum.     

Insecticide resistance in Helicoverpa armigera in South India

Cypermethrin, quinalphos, endosulfan and methomyl were bioassayed against strains of Helicoverpa armigera collected from field crops in Andhra Pradesh and Tamil Nadu, South India, during the 1989-90 and 1990-91 cropping seasons. In 1989, high levels of resistance to cypermethrin were recorded in strains from cotton in the cotton-growing regions of Guntur, Andhra Pradesh and Coimbatore, Tamil Nadu, and from pigeon pea near Hyderabad. There was no evidence for resistance to quinalphos or methomyl at that time. In 1990-91 sampling was more extensive and although tolerance to cypermethrin was lower than the previous season, the survey indicated that pyrethroid-resistant populations were present throughout much of Andhra Pradesh. Tolerance to quinalphos had increased slightly in 1990-91, while resistance to methomyl had increased substantially, particularly in the cotton-growing area of Guntur. Endosulfan tolerance had increased slightly compared to strains tested in 1986-88 in an earlier study. The geographic and temporal variations in severity of pyrethroid resistance in H. armigera in Andhra Pradesh are believed to arise because of dynamic interactions between local selection pressure and immigration of resistant and susceptible moths at certain times of the year.     

Status of Insecticide Resistance in Spodoptera litura in Andhra Pradesh,India

Twenty-two strains of the tobacco caterpillar, Spodoptera litura (F.) (Lepidoptera: Noctuidae), collected from groundnut crops of eight locations in Andhra Pradesh, India, between 1991 and 1996 were assayed in the F1 generation for resistance to commonly used insecticides. Resistance levels ranged as follows: cypermethrin, 0·2- to 197-fold; fenvalerate, 8- to 121-fold; endosulfan, 1-to 13-fold; quinalphos, 1- to 29-fold; monocrotophos, 2- to 362-fold and methomyl, 0·7- to 19-fold. In nearly all strains pre-treatment with the metabolic inhibitor, piperonyl butoxide, resulted in complete suppression of cypermethrin resistance (2- to 121-fold synergism), indicating that enhanced detoxification by microsomal P450-dependent monooxygenases was probably the major mechanism of pyrethroid resistance. Pre-treatment with the synergist DEF, an inhibitor of esterases and the glutathione S-transferase system, resulted in a 2- to 3-fold synergism with monocrotophos indicating that esterases and possibly glutathione S-transferases were at least to some extent contributing to organophosphate resistance. © 1997 SCI.     

Inhibition by aluminum of mycelial growth and of sporangial production and germination inPhytophthora infestans

Mycelial growth on clarified V8 agar of the potato late blight pathogenPhytophthora infestans was inhibited when either aluminum chloride (AlCl₃, 6 H₂O) or aluminum sulfate (Al₂(SO₄)₃, 18 H₂O) was added to the culture medium at concentrations of 2.5–100 mg.l^–1 Al³⁺. Toxicity of Al³⁺ varied among the fiveP. infestans isolates tested, but toxicity of sulfate and chloride salts was similar for a given isolate. Overall sporangial production was affected in all five isolates by both Al³⁺ forms. Al³⁺ also decreased sporangial germination at concentrations equal to or greater than 10 mg.l^–1 in two isolates. These data support the hypothesis of aluminum toxicity as a major factor in soil suppressiveness toP. infestans.     

Inactivation of soil-borne plant pathogens during small-scale composting of crop residues

Samples of heavily infested crop residues were incorporated in static compost heaps (2.5–4.6 m³) of the Indore type. Temperature increased to 50–70°C within 6 days depending on the type of crop residues used and the location within the heap. The heat phase (>40 °C) lasted 2–3 weeks and was followed by a c. 5-months maturation phase (<40 °c).=" among=" the=" 17=" pathogens=" tested,=">Olpidium brassicae and one of the four formae speciales ofFusarium oxysporum that were tested survived composting, but also their inoculum was greatly reduced.Survival during specific phases of composting was studied by incorporation and retrieval of samples at various stages of the process.F. oxysporum f. sp.melonis was completely inactivated andO. brassicae andPlasmodiophora brassicae were almost completely inactivated during the short heat phase. The three pathogens survived the long-lasting maturation phase without loss of viability. Heat evolved during composting was found to be the most important factor involved with sanitation of crop residues. The possible involvement of fungitoxic conversion products and microbial antagonism is discussed.     

The pyrethrins and related compounds. Part XXII. Preparation of isomeric cyano-substituted 3-phenoxybenzyl esters

Preparation of 3-phenoxybenzyl chrysanthemates and their dihalovinyl analogues substituted with a cyano group at the 2-, 6-, (R)-α-, or (S)-α- positions is described. The (R)- and (S)- isomers of α-cyano-3-phenoxybenzyl esters of 2,2-difluoro-, -dichloro-, and -dibromo-vinyl analogues of cis- and trans- chrysanthemic acid are separated chromatographically, as are the separate pairs of enantiomers of fenvalerate, (RS)-α- cyano-3-phenoxybenzyl (RS)-2-(4-chlorophenyl)-3-methylbutyrate. An optically active ester of α-cyano-3-phenoxybenzyl alcohol (obtained using D -oxynitrilase) with 2,2,3,3-tetramethylcyclopropanecarboxylic acid is synthesised.     

Pre-emergence herbicides for the control of broomrape (Orobanche cernua Loefl.) in sunflower (Helianthus annus L.)

Field experiments were conducted from 1989 to 1992 to determine the effects of pre-emergence herbicides in sunflower (Helianthus armuus L.) on: (1) the control of Orobanche cemua Loefl. (broomrape) and (2) crop damage and crop yield. Herbicides tested belong to the imidazolinone, sulfonylurea and substituted amide families. Imazethapy r (20–40 g ha^?1), imazapy r (12.5–25 gha^?1) and chlorsulfuron (4–6 gha^?1) controlled broomrape efficiently without crop injury. With good O. cernua control and good crop tolerance, sunflower seed yield from these treatments were generally similar to the non-infested checks and higher than the infestedchecks. Imazaquin (20–40 gha^?1), triasulfuron(4gha^?1), pdmisulfuron(3g ha^?1), acetochlor (4–4 kg ha^?1) and metazachlor (2 kg ha^?1) were less effective. Imazamethabenz (200–600 g ha^?1) and metolachlor (3–3 kg ha^?1) were ineffective. Wetconditions aftercropsowing considerably decreased O. cemua control with pre-emergence herbicides probably caused by enhanced degrädation. Des herbicides de prelevee pour la lutte contre Vorobanche (Orobanche cemua Loefl.) dans le toumesol (Helianthus annuus L.) Des expérimentations au champ ont été conduites de 1989 á 1992 pour determiner les effets d'herbicides de pré1evée du toumesol sun (a) la destruction de l'orobanche (Orobanche cernua Loefl.) et (b) la phytotoxcité sur la culture. Les herbicides testés appartenaient aux imidazolinones, aux sulfonylurdes et aux amides substituées. L'imazethapyr (20 á 40 gha^?1), l'imazapyr (12,5 á25gha^?1)et le chlorsulfuron (4 á 6 gha^?1) détruisaient efficacement l'orobanche sans occasionner de phytotoxidt6 sur la culture. Dans ces conditions, les rendements étaient généralement semblables à ceux des témoins non infestés et supérieurs à ceux des témoins infestés. L'imazaquin (20 à 40 g ha^?1), le triasulfuron (4 gha^?1), le primisulfuron (3 g ha^?1), lacétolachlor (4,4 kg ha^?1) et le métazachlor (2 kg ha^?1) étaient moins efficaces. L'imazaméthabenz (200 á 600 g ha^?1) et le métolachlor (3,3 kg ha^?1) etaient inefficaces. Des conditions humides aprfes le semis diminuaient considérablement la destruction de O. cemua par les herbicides de prélevée, probablement à cause d'une dégradation plus élevée. Vorauflaufherbigide zur Bekdmpfung der Sommerwurz Orobanche cemua Loefl. in Sonnenblume (Helianthus annuus L.) Zwischen 1989 und 1992 wurden in Sonnenblume Feldversuche zur Wirkung von Vorauflaufherbiziden aus den Gruppen der Imidazolinone, Sulfonylharnstoffe und substitutierten Amide auf die Sommerwurz Orobanche cernua und auf Kulturpflanzenschaden sowie den Ertrag durchgefuhrt. Mit Imazethapyr (20 bis 40 g ha^?1), Imazapyr (12,5 bis 25 g ha^?1) und Chlorsulfuron (4 bis 6 g ha^?1) lieβ sich die Sommerwurz wirksam bekampfen, ohne daβ Schaden an der Sonnenblume auftraten, und die Ertrage waren allgemein ahnlich oder hoher als bei der nichtparasitierten Kontrolle. Imazaquin (20 bis 40 ha^?1), Triasulfuron (4 g ha^?1).Primisulfuron (3 g ha ^?1). Acetochlor (4,4 kg ha ^?1 und Metazachlor (2 kg ha ^?1) waren weniger wirksam. Imazamethabenz (200 bis 600 g ha^?1) und Metolachlor (3,3 kg ha^?1) hatten keine Wirkung. Bei Niederschlagen nach der Saat der Sonnenblume war die Bekampfung der Sommerwurz mit Vorauflaufherbiziden vermutlich wegen verstärkten Abbaus erheblich schwächer.     

Independent and joint biological activity of isomeric forms of synthetic pyrethroids

Various isomeric mixtures of pyrethroids were examined in topical application tests against houseflies, Musca domestica. On the basis of the activities of the separate isomers of 5-benzyl-3-furylmethyl (±)-cis,trans-chrysanthemate, it was shown that when combined in pairs to give the (±)-trans or (±)-cis or (+)-cis,trans mixtures the observed mortalities did not differ from those expected by simple additive action calculated by the harmonic mean. In contrast the (±)-cis,trans mixture showed considerable antagonism with a mortality only 60% of that expected. Similar evaluations using the separate and combined isomers of bioallethrin [(R,S)-3-allyl-2-methyl-4-oxocyclopent-2-enyl (allethronyl) ( + )-trans-[(1R,3R)-chrysanthemate] and the corresponding (+)-cis-(1R,3S)-chrysanthemate indicate antagonism calculated to be correlated with the content of the (R)-isomer of the alcoholic moiety. Hence the activity of the most active isomer of the “allethrin” series, (S)-3-allyl-2-methyl-4-oxocyclopent-2-enyl ( + )-trans-(1R,3R)-chrysanthemate, (S)-bioallethrin, is not fully realised unless it is present in pure form and a substantial part of the value of bioresmethrin (5-benzyl-3-furylmethyl ( + )-trans-chrysanthemate] as a killing agent is lost when the racemic form is used. In racemic mixtures there is mutual antagonism between pairs of isomers so that considerable masking of activity occurs.     

UV protectants for Candida oleophila (strain O), a biocontrol agent of postharvest fruit diseases

This study investigated the influence of UV‐B radiation (280–320 nm) on survival of Candida oleophila strain O, an antagonist yeast that prevents postharvest diseases caused by Botrytis cinerea and Penicillium expansum on apple and pear fruits. Lethal doses (LD₅₀ and LD₉₀) were, respectively, 0·89 and 1·45 Kj m^?2 for in vitro exposure and 3·06 and 5·5 Kj m^?2 for in vivo exposure. A screening test of UV‐B protectants for strain O was also evaluated under in vitro and in vivo conditions. The in vitro results showed that sodium ascorbate (0·1% and 0·01%), riboflavin (0·1%) and uric acid (0·1% and 0·01%) were the most effective and most suitable protectants. However, only riboflavin (0·1%) and uric acid (0·1%) were effective under in vivo conditions. The efficacy obtained with strain O against P. expansum, when subjected to UV‐B radiation, was 75·0% and 49·2% for pathogen concentrations of 10⁵ and 10⁶ spores mL^?1, respectively. Adding riboflavin to strain O gave a similar efficacy (64·2%). Applying strain O together with uric acid (0·1%) was less active (47·7%). Nonetheless, its efficacy when applied with the antioxidants sodium ascorbate (71·1%) or ascorbic acid (82·5%) was the greatest. Riboflavin and uric acid were the most cost‐effective protectants, and could be included in the final formulation of strain O when applied preharvest.     

Locating quantitative trait loci associated with Orobanche crenata resistance in pea

Orobanche crenata (broomrape) is a root parasite that represents the major constraint for pea (Pisum sativum) cultivation in the Mediterranean area and the Middle East. The efficacy of available control methods is minimal and breeding for O. crenata resistance is considered the most promising strategy of control. Only moderate levels of incomplete resistance are available in pea germplasm. In order to identify and map the quantitative trait loci (QTL) controlling the trait, 115 F₂ plants derived from the cross between a susceptible and a resistant parent were analysed using isozymes, random amplified polymorphic DNA and sequence tagged site markers. F₂‐derived F₃ lines were studied for O. crenata resistance under field conditions. The linkage map was constructed with MAPMAKER V2.0. Of 217 markers, 120 could be mapped into 21 linkage groups. Linkage groups consisted of 13 to two marker loci covering 1770 cM. The mean inter‐marker distance was 17.64 cM. Simple interval mapping (SIM) and composite interval mapping (CIM) were performed using QTL Cartographer. The CIM approach using five cofactors was clearly the most efficient way to locate putative QTL. Two QTL for O. crenata resistance (Ocp1 and Ocp2), explaining only a moderate portion of the observed variation (9.6% and 11.4% respectively), were detected.     

Acaricidal activities of the active component of Lycopus lucidus oil and its derivatives against house dust and stored food mites (Arachnida: Acari)

BACKGROUND: Recent studies have focused on materials derived from plant extracts as mite control products against house dust and stored food mites because repeated use of synthetic acaricides had led to resistance and unwanted activities on non‐target organisms. The aim of this study was to evaluate the acaricidal activity of materials derived from Lycopus lucidus against Dermatophagoides farinae, D. pteronyssinus and Tyrophagus putrescentiae. RESULTS: The LD₅₀ values of L. lucidus oil were 2.19, 2.25 and 8.45 µg cm^?2 against D. farinae, D. pteronyssinus and T. putrescentiae. The acaricidal constituent of L. lucidus was isolated by chromatographic techniques and identified as 1‐octen‐3‐ol. In a fumigant method against D. farinae, the acaricidal activity of 1‐octen‐3‐ol (0.25 µg cm^?2) was more toxic than N,N‐diethyl‐m‐toluamide (DEET) (36.84 µg cm^?2), followed by 3,7‐dimethyl‐1‐octen‐3‐ol (0.29 µg cm^?2), 1‐octen‐3‐yl butyrate (2.32 µg cm^?2), 1‐octen‐3‐yl acetate (2.42 µg cm^?2), 3,7‐dimethyl‐1‐octene (9.34 µg cm^?2) and benzyl benzoate (10.02 µg cm^?2). In a filter paper bioassay against D. farinae, 1‐octen‐3‐ol (0.63 µg cm^?2) was more effective than DEET (20.64 µg cm^?2), followed by 3,7‐dimethyl‐1‐octen‐3‐ol (1.09 µg cm^?2). CONCLUSION: 1‐Octen‐3‐ol and 3,7‐dimethyl‐1‐octen‐3‐ol could be useful as natural agents for the management of three mite species. Copyright © 2011 Society of Chemical Industry