WO2003020030A1 - Attractif synthetique de lepidoptere attaquant les fruits - Google Patents

Attractif synthetique de lepidoptere attaquant les fruits Download PDF

Info

Publication number
WO2003020030A1
WO2003020030A1 PCT/AU2002/001203 AU0201203W WO03020030A1 WO 2003020030 A1 WO2003020030 A1 WO 2003020030A1 AU 0201203 W AU0201203 W AU 0201203W WO 03020030 A1 WO03020030 A1 WO 03020030A1
Authority
WO
WIPO (PCT)
Prior art keywords
attractant formulation
moth
component
fruitpiercing
formulation
Prior art date
Application number
PCT/AU2002/001203
Other languages
English (en)
Inventor
Harry Angus Charles Fay
Keith Herbert Halfpapp
Original Assignee
The State Of Queensland Through Its Department Of Primary Industries
Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)
Filing date
Publication date
Application filed by The State Of Queensland Through Its Department Of Primary Industries filed Critical The State Of Queensland Through Its Department Of Primary Industries
Priority to AU2002331417A priority Critical patent/AU2002331417B2/en
Publication of WO2003020030A1 publication Critical patent/WO2003020030A1/fr

Links

Classifications

    • AHUMAN NECESSITIES
    • A01AGRICULTURE; FORESTRY; ANIMAL HUSBANDRY; HUNTING; TRAPPING; FISHING
    • A01NPRESERVATION OF BODIES OF HUMANS OR ANIMALS OR PLANTS OR PARTS THEREOF; BIOCIDES, e.g. AS DISINFECTANTS, AS PESTICIDES OR AS HERBICIDES; PEST REPELLANTS OR ATTRACTANTS; PLANT GROWTH REGULATORS
    • A01N37/00Biocides, pest repellants or attractants, or plant growth regulators containing organic compounds containing a carbon atom having three bonds to hetero atoms with at the most two bonds to halogen, e.g. carboxylic acids
    • A01N37/02Saturated carboxylic acids or thio analogues thereof; Derivatives thereof

Definitions

  • TITLE "SYNTH ETIC FRU ITPI ERCI NG MOTH ATTRACTANT" FI ELD OF I NVENTI ON TH IS I NVENTION relates to a synthetic fruitpiercing moth attractant.
  • Fru itpiercing moths sometimes referred to as fruitsucking moths, belong to the genus Eudocima, which formerly included the genera Othreis, Rhytia, Khadira and Adris. They cause damage to around 50 different commercial fruit species resulting in substantial losses to growers through spoilt fruit.
  • the adult moth penetrates the skin or rind of fruit with a barbed proboscis and the extensive probing for juice destroys a large area of tissue beneath the surface.
  • Fru itpiercing moths begin entering fruit crops to feed as soon as the first fruits ripen, as reported in Fay and Halfpapp,
  • Eudocima fullonia Eudocima salaminia
  • Eudocima materna Eudocima materna
  • Eudocima fullonia is the most prevalent species throughout these regions. Eudocima materna also occurs in parts of the
  • Orchard lighting systems wh ich employ green-yellow lights (550 - 580 ⁇ m), can suppress moth feeding. Tests in Australia, of such systems, have measured a 60-70% reduction in moth activity for medium to low population levels. Such systems require considerable investment in electrical infrastructure, in part due to the mandatory safety requirements imposed by energy authorities. These lighting systems do not control any additional pests from entering the area. For those regions where fruitpiercing moths are an irregular problem, such a technique is prohibitively expensive.
  • I nsecticidal cover sprays have never been widely employed against fruitpiercing moths, due to their lack of efficacy, problems with chemical residues arising from the lateness of application relative to crop harvest, and potential interference with the ongoing development of I ntegrated Pest Management (I PM), which is now well advanced in some crops.
  • Carbaryl used on citrus crops, is the only insecticide registered for use against fruitpiercing moths in Australia (as reported in QDPI : I NFOPEST Vers.2.5-Pest Management I nformation System, 2000). However, carbaryl has little efficacy against these moths.
  • Baiting based on organic feed ing attractants has long been used as a control method against fruitpiercing moths, but they have not provided sufficient mortality rates for use in commercial crops.
  • a number of reports namely Hargreaves, Bulletin of Entomological Research 1936, 27, 589-605; Baptist, Indian Journal of Entomology, 1944, 6, 1 -13; Yoon and Kim, Korean Journal of Plant Protection, 1977, 1 6, 127-131 ; Dodia et al. , Tamil Agricultural University Research Journal, 1986, 1 1 , 72-73, disclose the use of feeding attractants, which have included brown sugar, fruit (particularly overripe banana), fruit pulp or fruit juice, honey and beer (or other beverages).
  • Plant-derived attractants for adult moths are extensively referred to in the literature. Most relate to species, which are attracted to flowers, such as Gaura spp. , which attract Helicoverpa zea, as reported in Lingren et al. , Southwestern Entomologist, 1998, No. 21 .
  • Sex pheromones are generally species specific and so do not have the broad applicability of general feeding attractants.
  • the invention provides a synthetic fruitpiercing moth attractant formulation comprising;
  • Component (i) may be selected from one or more of amyl acetate, ethyl acetate, n-butyl acetate, hexyl acetate, methyl butyrate, ethyl butyrate, methyl caprylate, ethyl caproate, ethyl sorbate, and methyl anthranilate.
  • a preferable example of component (i) is methyl butanoate (CH 3 CH 2 CH 2 CO 2 CH 3 ).
  • Component (ii) may be selected from one or more of acetaldehyde, hexanal and trans-2-hexanal .
  • Component (iii) may be selected from one or more of ethanol , 1 -hexanol , cis-3-hexanol and 1 -butanol.
  • a preferable example of component (iii) is 1 -hexanol [CH 3 (CH 2 ) 5 ⁇ H].
  • the moth attractant formulation ranges comprise the following proportions of each of components (i) to (iii);
  • component (b) 0.1 % to 50% of component (ii);
  • component (c) 0.1 % to 50% of component (iii); whereby in each case the components (i), (ii) and (iii) add up to 100% or 1 00g of mixture on a weight/weight basis wherein each of the components are expressed in grams.
  • proportions of the abovementioned components (i), (ii) and (iii) are as follows: (a) 55-90% of component (i); and (b) 10-45% of component (ii); and/or
  • the proportion of the abovementioned components (i), (ii) and (iii) are as follows: (a) 75-80% of component (i); and (b) 1 5-25% of component (ii); and/or
  • the moth attractant formulation may further comprise one or more aromatic compounds, such as d-limonene.
  • concentrations of components (i), (ii) and (iii) are calculated on a dry weight basis without taking into consideration the amount of any solvent that may be used.
  • the solvents may include acetone, ethanol, hexane or pentane.
  • the word formulation as used herein refers to an admixture of one or more or the components (i) and (ii) and/or (iii) or where one or more of the components (i) and (ii) and/or (iii) are individually contained in separate areas or components of a bait so as in use to provide a volatile admixture of the components (i) and (ii) and/or (iii).
  • I n another form of the invention there is provided a synthetic fruitpiercing moth attractant formulation comprising, one or more straight chain and/or branched chain C 2 -C 1 2 aliphatic primary, secondary or tertiary esters and all isomers thereof
  • a method of attracting and/or controlling fru itpiercing moths by use of two or more straight chain and/or branched chain C 2 -C 12 aliphatic primary, secondary or tertiary esters and all isomers thereof, on or in the vicinity of a fruit crop.
  • I n another form of the invention there is provided a method of attracting and/or controlling insects by use of one of the above moth attractant formulations as a bait, trap or lure for fruitpiercing moths in the vicinity of a fruit crop.
  • the moth attractant formulations of the invention further includes a toxicant, chemosterilant, growth regulator or pathogen.
  • the moth attractant formulations when it is a bait may incorporate the moth attractant formulation as an admixture or having one or more of the components (i) and/or (ii) and/or (iii) individually contained within separate compartments or areas of the bait.
  • the moth lure may be a coated-gel , which incorporates the moth attractant formulation .
  • the gel may contain a preservative, such as sod ium benzoate, and/or 0 - 10% sucrose, as a feeding stimulant.
  • the gel might be used in a trap or as a free-access bait containing a toxicant, chemosterilant, growth regulator, or pathogen .
  • a preferable example of a toxicant is beta cyfluthrin, imidacloprid , or the like.
  • a preferable example of a chemosterilant is triethylenephosphoramide (TEPA), hexamethylphosphoric triamide (H EM PA), or the like.
  • a preferable example of a growth regulator is tebufenozide, fenoxycarb, or the like.
  • a preferable example of a pathogen is metarhizium , Nuclear Polyhedrosis Virus (NPV), or the like.
  • FIG 1 illustrates the d ifferential responses by two fruitpiercing moth species to a range of individual volatile compounds known to occur in fru it odou rs, as recorded on an electroantennogram (EAG).
  • EAG electroantennogram
  • FIG 2 shows the differences in the observed EAG responses of E. fullonia to combinations of volatiles to expected EAG responses as a proportion to the same compounds offered singly.
  • FIG 3 compares the numbers of fruitpiercing moths on different bait compositions.
  • component (i) being five 'general' fruity esters (amyl acetate, n-butyl acetate, ethyl butyrate, methyl butyrate and ethyl acetate), one 'specific' fru ity ester (methyl anthranilate);
  • component (ii) • three examples of component (ii), acetaldehyde, hexanal , trans- 2-hexanal; • four examples of component (iii), ethanol , 1 -hexanol , cis-3- hexanol and 1 -butanol,
  • FIG 1 provides a summary of the responses in millivolts of mature fed E. fullonia and E. materna to 2.5 ⁇ l of each compou nd .
  • Table 1 summarises the attractant formulations used in this example. There were four 'fruits' of a single type for each test, which included a control treatment with no volatiles added. Tests were conducted through a single night, and replicated on seven separate occasions. The percentage of each fruit type attacked was recorded for each occasion and the results analysed by ANOVAR and LSD(T) tests of means. 'Ripe' fruit were preferred , but not statistically more than the 'very ripe' type (Table 1 ). However, 'fru its' which contained a high proportion of the non-ester components were far less attractive.
  • Baits containing only esters (5 or 6 esters per bait) were compared against those that contained 80% esters (3 esters per bait) plus aldehydes and an alcohol in the citrus crop several times through a season .
  • Table 6 summarises the formulation details for each bait used on each occasion.
  • baits were placed in the citrus crop once a week in a six-week period .
  • Baits contained 80% esters (of 2-3 types), 15-18.9% aldehydes (of 1 -3 types) and 1 .1 -5.0% alcohols (1 type).
  • the commonest volatile components in the baits were n-butyl acetate, methyl butyrate, trans-2-hexenal and 1 -hexanol.
  • Table 7 summarises the formulation details for each bait type used . There were equal numbers of baited and u nbaited trees, and 2 baits of any treatment in any tree. Moth activity was observed in baited and unbaited trees for 2h after dark. E. fullonia was the dominant species active during the first half of the season and E. materna during the remainder.
  • FIG 3 compares the number of moths observed on baits with the number of moths observed on fruit on baited trees for a) all Eudocima spp. , and b) all Eudocima exclud ing E. materna.
  • E. materna were excluded for statistical purposes because they occur in lower numbers on the east coast of Australia.
  • the number of baits attacked was recorded after the first night and the numbers of moths on baits and fruit recorded on the third night of exposure. After the initial night's exposure, 30% of the standard baits had been attacked by fruitpiercing moths compared to 40% of the waxed baits. On the third night, 5 moths (all E. fullonia) were observed on the waxed baits and none on the standard ones, and one (1 ) E. fullonia was recorded on fruit on baited trees. After 3 nights, 90% of the waxed baits were found to be pierced compared to 50% of the standard baits. EXAMPLE 1 1
  • This experiment is similar to Example 10, except in that 2% glycerine and 2% paraffin oil was incorporated into the agar baits before waxing.
  • the glycerine and paraffin oil are used as extenders in the baits, i.e. they slow the release of the attractant.
  • 20% (of those without glycerine/paraffin) and 30% (of those with glycerine/paraffin) were attacked on night 1 , and 40% of both types had been attacked after night 2.
  • a fruitpiercing moth attractant formulation comprising; two or more of component (i) [ester] , components (i) and (ii) [ester and aldehyde] , components (i) and (iii) [ester and alcohol] and a formulation having a number of components (i), (ii) and (iii) are all efficacious in attracting fru itpiercing moths.
  • the fruitpiercing moth attractant formulation comprising of a single component (i), (ii) and (iii) would be efficacious in attracting and controlling fruitpiercing moths.

Abstract

L'invention concerne une formulation d'un attractif d'insectes comprenant (i) un ou plusieurs esters primaires, secondaires ou tertiaires aliphatiques C2-C12 à chaîne droite et/ou chaîne ramifiée et tous leurs isomères; et (ii) un ou plusieurs aldéhydes aliphatiques C2-C12 saturés ou insaturés et tous leurs isomères; et/ou (iii) un ou plusieurs alcools primaires, secondaires ou tertiaires aliphatiques C1-C12 saturés ou insaturés et tous leurs isomères. La formulation de cette invention est utilisée pour attirer et/ou lutter contre les insectes, plus particulièrement un lépidoptère attaquant les fruits, à proximité de cultures de fruits. L'invention concerne également une formulation d'un attractif synthétique de lépidoptères attaquant les fruits comprenant deux ou plusieurs esters primaires, secondaires ou tertiaires aliphatiques C2-C12 à chaîne droite et/ou chaîne ramifiée et tous leurs isomères, ainsi qu'un procédé permettant d'attirer et/ou lutter contre les lépidoptères attaquant les fruits grâce à l'utilisation d'au moins deux esters primaires, secondaires ou tertiaires aliphatiques C2-C12 à chaîne droite et/ou chaîne ramifiée et tous leurs isomères sur ou à proximité d'une culture de fruits.
PCT/AU2002/001203 2001-09-03 2002-09-03 Attractif synthetique de lepidoptere attaquant les fruits WO2003020030A1 (fr)

Priority Applications (1)

Application Number Priority Date Filing Date Title
AU2002331417A AU2002331417B2 (en) 2001-09-03 2002-09-03 Synthetic fruitpiercing moth attractant

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
AUPR7439 1998-12-02
AUPR7439A AUPR743901A0 (en) 2001-09-03 2001-09-03 Synthetic fruitpiercing moth attractant

Publications (1)

Publication Number Publication Date
WO2003020030A1 true WO2003020030A1 (fr) 2003-03-13

Family

ID=3831390

Family Applications (1)

Application Number Title Priority Date Filing Date
PCT/AU2002/001203 WO2003020030A1 (fr) 2001-09-03 2002-09-03 Attractif synthetique de lepidoptere attaquant les fruits

Country Status (2)

Country Link
AU (1) AUPR743901A0 (fr)
WO (1) WO2003020030A1 (fr)

Cited By (7)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
ES2239548A1 (es) * 2004-03-11 2005-09-16 Universidad Politecnica De Valencia Un cebo alimentario con atrayente especifico para combatir insectos tefritidos.
WO2006121317A1 (fr) * 2005-05-09 2006-11-16 El Colegio De La Frontera Sur Appat pour les mouches a fruit anastrepha obliqua
WO2010143752A3 (fr) * 2009-06-11 2011-02-24 International Centre Of Insect Physiology And Ecology Compositions destinées à attirer des insectes hématophages
KR101432627B1 (ko) 2006-09-13 2014-08-21 바이엘 크롭사이언스 아게 식물 독성이 감소된 제초제 조성물
CN110200020A (zh) * 2019-07-18 2019-09-06 重庆谷百奥生物研究院有限公司 杀虫组合物
WO2023288294A1 (fr) 2021-07-16 2023-01-19 Novozymes A/S Compositions et procédés pour améliorer la résistance à la pluie de protéines sur des surfaces de plantes
WO2023225459A2 (fr) 2022-05-14 2023-11-23 Novozymes A/S Compositions et procédés de prévention, de traitement, de suppression et/ou d'élimination d'infestations et d'infections phytopathogènes

Non-Patent Citations (5)

* Cited by examiner, † Cited by third party
Title
HANSSON B.S. ET AL.: "Comparison of male and female olfactory cell response to pheromone compounds and plant volatiles in the turnip moth, agrotis segetum", PHYSIOLOGICAL ENTOMOLOGY, vol. 14, 1989, pages 147 - 155 *
HERN A. AND DORN S.: "Induced emissions of apple fruit volatiles by the codling moth: changing patterns with different time periods after infestation and differential larval instars", PHYTOCHEMISTRY, vol. 57, 2001, pages 409 - 416 *
HERN A. AND DORN S.: "Statistical modelling of insect behavioural responses in relation to the chemical composition of test extracts", PHYSIOLOGICAL ENTOMOLOGY, vol. 26, no. 4, 2001, pages 381 - 390 *
PINERO J. ET AL.: "Using odor-baited traps to capture immigrating plum curculios", FRUIT NOTES, vol. 65, 2000, pages 42 - 44 *
WOOD D.L. ET AL.: "Control of Insect Behavior by Natural Products", 1970, ACADEMIC PRESS, NEW YORK, LONDON, article "Insect attractants of vegetable origin, with special reference to the rice stem borer and fruit-piercing moths", pages: 225 - 235 *

Cited By (10)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
ES2239548A1 (es) * 2004-03-11 2005-09-16 Universidad Politecnica De Valencia Un cebo alimentario con atrayente especifico para combatir insectos tefritidos.
WO2005086999A1 (fr) * 2004-03-11 2005-09-22 Universidad Politecnica De Valencia Appat alimentaire comprenant un attractif specifique pour lutter contre les insectes de la famille des tephrites
AU2005220625B2 (en) * 2004-03-11 2011-08-04 Universidad Politecnica De Valencia Food bait comprising a specific attractant for combating tephritidae insects
WO2006121317A1 (fr) * 2005-05-09 2006-11-16 El Colegio De La Frontera Sur Appat pour les mouches a fruit anastrepha obliqua
KR101432627B1 (ko) 2006-09-13 2014-08-21 바이엘 크롭사이언스 아게 식물 독성이 감소된 제초제 조성물
WO2010143752A3 (fr) * 2009-06-11 2011-02-24 International Centre Of Insect Physiology And Ecology Compositions destinées à attirer des insectes hématophages
CN102711458A (zh) * 2009-06-11 2012-10-03 昆虫生态学及生理学国际中心 用于吸引吸血昆虫的组合物
CN110200020A (zh) * 2019-07-18 2019-09-06 重庆谷百奥生物研究院有限公司 杀虫组合物
WO2023288294A1 (fr) 2021-07-16 2023-01-19 Novozymes A/S Compositions et procédés pour améliorer la résistance à la pluie de protéines sur des surfaces de plantes
WO2023225459A2 (fr) 2022-05-14 2023-11-23 Novozymes A/S Compositions et procédés de prévention, de traitement, de suppression et/ou d'élimination d'infestations et d'infections phytopathogènes

Also Published As

Publication number Publication date
AUPR743901A0 (en) 2001-09-27

Similar Documents

Publication Publication Date Title
Vayssieres et al. Effectiveness of spinosad bait sprays (GF-120) in controlling mango-infesting fruit flies (Diptera: Tephritidae) in Benin
James Further field evaluation of synthetic herbivore-induced plan volatiles as attractants for beneficial insects
Segura et al. Plant chemicals and the sexual behavior of male tephritid fruit flies
Cardé et al. Disruption of sexual communication in Laspeyresia pomonella 1 (codling moth), Grapholitha molesta 1 (Oriental fruit moth) and G. Prunivora 1 (lesser appleworm) with hollow fiber attractant sources
US20090281190A1 (en) Novel attract and kill composition for control of pest insects
Böckmann et al. Bait spray for control of European cherry fruit fly: an appraisal based on semi‐field and field studies
US20210321627A1 (en) Non-pesticidal attract and kill composition for control of insects
Chinajariyawong et al. Efficacy of protein bait sprays in controlling fruit flies (Diptera: Tephritidae) infesting angled luffa and bitter gourd in Thailand
US3186903A (en) Synergistic pyrethrum insecticide
WO2003020030A1 (fr) Attractif synthetique de lepidoptere attaquant les fruits
Salom et al. Laboratory evaluation of biologically-based compounds as antifeedants for the Pales weevil, Hylobius pales (Herbst)(Coleoptera: Curculionidae)
EP2572579B1 (fr) Compositions pour attirer des Tortricidae (les tordeuses)
AU2008229734B2 (en) Insect attractant composition
EP0333747B1 (fr) Formule de pheromone amelioree
Klein Mass trapping for suppression of Japanese beetles
DE102004004900B4 (de) Verwendung einer Zusammensetzung als Attraktans für Gartenlaubkäfer (Phyllopertha horticola)
Oehlschlager Current status of trapping palm weevils and beetles
RU2739080C2 (ru) Композиция для привлечения и успокаивания пчел и ее применение в сельском хозяйстве, садоводстве и пчеловодстве
AU2002331417B2 (en) Synthetic fruitpiercing moth attractant
Ioriatti et al. Control of codling moth by attract and kill
Ekesi Baiting and male annihilation techniques for fruit fly suppression in Africa
AU2002331417A1 (en) Synthetic fruitpiercing moth attractant
Karg et al. Applied aspects of insect olfaction
Cook et al. The native anthocorid bug (Orius armatus) as a field predator of Frankliniella occidentalis in Western Australia
US4929441A (en) Unnatural sex attractants for male pink bollworms and pinkspotted bollworms and use thereof

Legal Events

Date Code Title Description
AK Designated states

Kind code of ref document: A1

Designated state(s): AE AG AL AM AT AU AZ BA BB BG BY BZ CA CH CN CO CR CU CZ DE DM DZ EC EE ES FI GB GD GE GH HR HU ID IL IN IS JP KE KG KP KR LC LK LR LS LT LU LV MA MD MG MN MW MX MZ NO NZ OM PH PL PT RU SD SE SG SI SK SL TJ TM TN TR TZ UA UG US UZ VC VN YU ZA ZM

Kind code of ref document: A1

Designated state(s): AE AG AL AM AT AU AZ BA BB BG BR BY BZ CA CH CN CO CR CU CZ DE DK DM DZ EC EE ES FI GB GD GE GH GM HR HU ID IL IN IS JP KE KG KP KR KZ LC LK LR LS LT LU LV MA MD MG MK MN MW MX MZ NO NZ OM PH PL PT RO RU SD SE SG SI SK SL TJ TM TN TR TT TZ UA UG US UZ VC VN YU ZA ZM ZW

AL Designated countries for regional patents

Kind code of ref document: A1

Designated state(s): GH GM KE LS MW MZ SD SL SZ UG ZM ZW AM AZ BY KG KZ RU TJ TM AT BE BG CH CY CZ DK EE ES FI FR GB GR IE IT LU MC PT SE SK TR BF BJ CF CG CI GA GN GQ GW ML MR NE SN TD TG

Kind code of ref document: A1

Designated state(s): GH GM KE LS MW MZ SD SL SZ TZ UG ZM ZW AM AZ BY KG KZ MD RU TJ TM AT BE BG CH CY CZ DE DK EE ES FI FR GB GR IE IT LU MC NL PT SE SK TR BF BJ CF CG CI CM GA GN GQ GW ML MR NE SN TD TG

DFPE Request for preliminary examination filed prior to expiration of 19th month from priority date (pct application filed before 20040101)
121 Ep: the epo has been informed by wipo that ep was designated in this application
WWE Wipo information: entry into national phase

Ref document number: 2002331417

Country of ref document: AU

122 Ep: pct application non-entry in european phase
NENP Non-entry into the national phase

Ref country code: JP

WWW Wipo information: withdrawn in national office

Country of ref document: JP