WO2001037664A1 - Diamondback moth pheromone composition - Google Patents

Diamondback moth pheromone composition Download PDF

Info

Publication number
WO2001037664A1
WO2001037664A1 PCT/AU2000/001417 AU0001417W WO0137664A1 WO 2001037664 A1 WO2001037664 A1 WO 2001037664A1 AU 0001417 W AU0001417 W AU 0001417W WO 0137664 A1 WO0137664 A1 WO 0137664A1
Authority
WO
WIPO (PCT)
Prior art keywords
composition
pheromone
traps
hexadecenol
diamondback
Prior art date
Application number
PCT/AU2000/001417
Other languages
French (fr)
Inventor
Richard Alan Vickers
Original Assignee
Commonwealth Scientific And Industrial Research Organisation
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 Commonwealth Scientific And Industrial Research Organisation filed Critical Commonwealth Scientific And Industrial Research Organisation
Priority to AU15041/01A priority Critical patent/AU1504101A/en
Publication of WO2001037664A1 publication Critical patent/WO2001037664A1/en

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
    • 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
    • A01N37/04Saturated carboxylic acids or thio analogues thereof; Derivatives thereof polybasic

Definitions

  • the present invention relates to a composition for use as an attractant for diamondback moths.
  • the composition may be used as the attractant in traps and may also be used to disrupt mating of diamondback moths.
  • the present invention further relates to methods of trapping and disrupting mating of diamondback moths using the composition.
  • the binary pheromone mixture has proved quite effective as an attractant in traps. Any possible enhancement in trap catches obtained by adding a synergist has therefore not been an issue in the context of monitoring.
  • the binary mixture has, however, also been used to try to disrupt mating of the insect and in this case the exact composition of the pheromone may be critical. It was successful in reducing damage to crops but the amounts required to achieve an effective level of control were very high. This made the application of mating disruption techniques to control this insect uneconomic under most circumstances.
  • the present invention provides a synthetic pheromone composition for use as an attractant for diamondback moths comprising (Z)-ll-hexadecenyl acetate, (Z)-ll hexadecenal and (Z)-ll-hexadecenol in a weight/weight ratio of 10:2-25 :1-5.
  • the present invention provides a synthetic pheromone composition
  • a synthetic pheromone composition comprising (Z)-ll-hexadecenyl acetate, (Z)-ll-hexadecenal and (Z)-ll-hexadecenol in a weight/weight ratio of 10:2-25:1-10.
  • the weight/weight ratio is 10:5-15 :2-5, more preferably.
  • the composition according to the present invention may be used as an attractant for diamondback moths in traps.
  • the amount of the composition that may be used to bait such traps may be 50 to 2000 ⁇ g/trap, preferably 100 to l,000 ⁇ g/trap.
  • the compositions may include a suitable solvent such as cyclohexane. Since the composition of the invention more closely resembles the natural pheromone composition than previous binary mixtures, it is anticipated that the present composition will also offer advantages in the application of disrupting mating of diamondback moths. In particular, it is believed that lesser, more economic, amounts of the composition will be sufficient.
  • composition is used for disrupting mating
  • a suitable insecticide e.g. fibronil
  • insecticide application may be used to help reduce pest populations to a level where mating disruption would be more effective.
  • the composition when used as a mating disruptant may include a suitable solvent such as cyclohexane. Dispensing of the composition for the disruption of mating may be achieved using dispensers known to the art. The composition may be dispensed from such dispensers at a rate of about
  • the present invention provides a method of trapping diamondback moths comprising the step of providing an infested area with one or more insect traps containing an amount of a composition according to the first aspect.
  • the present invention provides a method of controlling the proliferation of diamondback moths, comprising the step of dispensing within an infested area an amount of a composition according to the first aspect, said amount being suitable to disrupt diamondback moth mating.
  • composition and methods according to the invention thereby offer potential for reducing the damage caused to cruciferous crops (e.g. cabbage, cauliflower, brussel sprouts, broccoli, etc.) by diamondback moth larvae.
  • cruciferous crops e.g. cabbage, cauliflower, brussel sprouts, broccoli, etc.
  • Figure 1 provides a gas chroma tograph trace (Trace A00445) of an extract of P. xjdostella pheromone glands. Trace A00444 is from an extract of other body tissues.
  • Figure 2 provides graphical results for trap catches using Compositions
  • Figure 3 provides graphical results for trap catches using Compositions J and L described hereinafter.
  • Example 1 Analysis of an extract of Plutella xylostella pheromone glands
  • Koshihara and Yamada (1977) used an indirect method of collection in which a number of female insects were allowed to release the pheromone inside a glass flask. The pheromone deposited on the walls was then collected using a solvent. In the present instance, it was decided instead to excise pheromone glands from the females and extract the pheromone from the glands.
  • Each method has advantages and disadvantages. The present choice was based on the fact that there was available methods for purifying the pheromone which removes most of the troublesome impurities.
  • a method to discriminate between pheromone components and impurities using computer manipulated graphics to facilitate the comparison of GC traces was developed.
  • Direct extraction from the glands also minimizes the oxidation and other decomposition of pheromone products which can occur by the indirect method. This was important because one of the components reported by Koshihara and Yamada (1977) is an aldehyde which is a relatively unstable compound.
  • Example 2 Formulation of synthetic pheromone compositions and field trials
  • Example 1 of the third component (C) does not in itself prove that it is a behaviourally active component of the P. xylostella pheromone. That is, it is possible that the third component was a precursor of one of the other components so that its presence might be coincidental. The best way of determining whether it actually contributes directly to the attraction is by a bioassay in which the old binary blend is compared with the new formulation containing the third component. Trapping of insects in an infested field using sticky traps baited with different pheromone compositions was considered the quickest and most effective method to resolve the matter.
  • the traps were constructed from waxed cardboard, measuring 85mm from base to apex and housed a replacable Tanglefoot E -coated liner, 90mm wide and 170mm long that was fixed to the base with a paper clip.
  • Baits consisted of 100 ⁇ g of pheromone dissolved in 10 ⁇ l of cyclohexane applied to the lumen of a 20mm length of surgical rubber tubing (internal diameter: 4.5mm. outer diameter: 6.5mm) placed centrally on the liner.
  • Each trap contained the binary blend at two different ratios and two different formulations of a blend including (Z)-ll-hexadecenol. So as not to overwhelm the traps and to enhance any positive effect all the baits were made up with a concentration one tenth that normally used in commercial baits used for monitoring purposes. This was set up in a field of brussel sprouts in South Australia. The experiment was replicated three times using fresh baits. The numbers of insects caught at the different traps clearly showed that the formulations including (Z)-ll-hexadecenol was much more attractive to the insects than the old binary blend (Table 1).
  • composition as follows:
  • compositions C and D are more attractive than either A or B with a greater than 99.9% probability.
  • Virgin females derived from a laboratory culture were placed individually in small cylinders with mesh-covered ends and were suspended from the underside of the lids covering the water traps. The protocol called for replacement of females when they died. Catches were recorded 2 to 3 times each week over the period of the trial (58 days).
  • compositions including (Z)-ll-hexadecenol out performs the old binary compositions by a factor of 4-10 as measured by the number of insects which are attracted into a trap.

Landscapes

  • Life Sciences & Earth Sciences (AREA)
  • Agronomy & Crop Science (AREA)
  • Pest Control & Pesticides (AREA)
  • Plant Pathology (AREA)
  • Health & Medical Sciences (AREA)
  • Engineering & Computer Science (AREA)
  • Dentistry (AREA)
  • General Health & Medical Sciences (AREA)
  • Wood Science & Technology (AREA)
  • Zoology (AREA)
  • Environmental Sciences (AREA)
  • Agricultural Chemicals And Associated Chemicals (AREA)
  • Catching Or Destruction (AREA)

Abstract

A composition for use as an attractant for diamondback moths is disclosed comprising (Z)-11-hexadecenyl acetate, (Z)-11-hexadecenal and (Z)-11-hexadecenol and, optionally, a suitable solvent. The composition may be used as the attractant in traps and may also be used to disrupt mating of diamondback moths.

Description

DIAMONDBACK MOTH PHEROMONE COMPOSITION
Field of the Invention:
The present invention relates to a composition for use as an attractant for diamondback moths. The composition may be used as the attractant in traps and may also be used to disrupt mating of diamondback moths. The present invention further relates to methods of trapping and disrupting mating of diamondback moths using the composition.
Background of the Invention:
The composition of the sex pheromone of Diamondback moth, Plutella
Figure imgf000002_0001
was reported in 1977 by Tamaki and co-workers who proposed a binary mixture containing equal amounts of (Z)-ll-hexadecenyl acetate and (Z)-ll-hexadecenyl aldehyde. This proved attractive to insects in the field and a number of publications followed, especially field studies, using this mixture. Koshihara & Yamada (1980) showed however that the attractancy of the baits could be increased considerably if small amounts of other compounds were added to the binary mixture. Similar synergistic effects were observed by other workers (e.g. Chisholm et al. 1982). The binary pheromone mixture has proved quite effective as an attractant in traps. Any possible enhancement in trap catches obtained by adding a synergist has therefore not been an issue in the context of monitoring. The binary mixture has, however, also been used to try to disrupt mating of the insect and in this case the exact composition of the pheromone may be critical. It was successful in reducing damage to crops but the amounts required to achieve an effective level of control were very high. This made the application of mating disruption techniques to control this insect uneconomic under most circumstances.
The synergistic effect of a range of other compounds and the large amounts of the binary mixture required for mating disruption could be judged to indicate, as Koshihara & Yamada (1980) themselves speculated, that the binary mixture is incomplete. Alternatively one of its components could have been incorrectly identified. While it may have been expected that if other components are present they would have been found by now, there is no published evidence for any recent re-investigation of the sex pheromone of this insect. The big difference between 1977 and now lies in the instrumentation available for pheromone blend analysis. Gas chromatography (GC) has been revolutionised by the appearance of capillary columns which have largely replaced the older packed columns providing much higher resolution and sensitivity. Minor components which may have been missed by Tamaki et al. (1977) would most likely be easily detectable with modern instruments.
Based on the information presented above, it was thought to be worthwhile carrying out a new chemical analysis of the contents of the sex pheromone gland of P. xj ostella females using gas chromatography. As a result of this analysis, the present inventors have found a component in addition to the two components of the binary mixture proposed by Tamaki et al. (1977). This additional component corresponds to one of the compounds on the list found by Koshihara & Yamada (1980) to increase the numbers of insects caught in traps when added to the binary mixture. In further work presented hereinafter, the present inventors have identified relative amounts of the three components which provide compositions demonstrating improved attraction in traps as compared to previous binary mixtures.
Summary of the Invention:
The present invention provides a synthetic pheromone composition for use as an attractant for diamondback moths comprising (Z)-ll-hexadecenyl acetate, (Z)-ll hexadecenal and (Z)-ll-hexadecenol in a weight/weight ratio of 10:2-25 :1-5.
Detailed Description of the Invention:
In a first aspect, the present invention provides a synthetic pheromone composition comprising (Z)-ll-hexadecenyl acetate, (Z)-ll-hexadecenal and (Z)-ll-hexadecenol in a weight/weight ratio of 10:2-25:1-10. Preferably, the weight/weight ratio is 10:5-15 :2-5, more preferably.
10:10:4.
The composition according to the present invention may be used as an attractant for diamondback moths in traps. The amount of the composition that may be used to bait such traps may be 50 to 2000μg/trap, preferably 100 to l,000μg/trap. The compositions may include a suitable solvent such as cyclohexane. Since the composition of the invention more closely resembles the natural pheromone composition than previous binary mixtures, it is anticipated that the present composition will also offer advantages in the application of disrupting mating of diamondback moths. In particular, it is believed that lesser, more economic, amounts of the composition will be sufficient.
Where the composition is used for disrupting mating, it may be advantageous to use the composition in conjunction with a suitable insecticide (e.g. fibronil), particularly when pest populations are high. That is, insecticide application may be used to help reduce pest populations to a level where mating disruption would be more effective. As with the use as a trap bait, the composition when used as a mating disruptant may include a suitable solvent such as cyclohexane. Dispensing of the composition for the disruption of mating may be achieved using dispensers known to the art. The composition may be dispensed from such dispensers at a rate of about
5-100 mg/ha/hour.
In a second aspect, the present invention provides a method of trapping diamondback moths comprising the step of providing an infested area with one or more insect traps containing an amount of a composition according to the first aspect.
In a third aspect, the present invention provides a method of controlling the proliferation of diamondback moths, comprising the step of dispensing within an infested area an amount of a composition according to the first aspect, said amount being suitable to disrupt diamondback moth mating.
The composition and methods according to the invention thereby offer potential for reducing the damage caused to cruciferous crops (e.g. cabbage, cauliflower, brussel sprouts, broccoli, etc.) by diamondback moth larvae.
Throughout this specification the word "comprise"., or variations such as "comprises" or "comprising", will be understood to imply the inclusion of a stated element, integer or step, or group of elements, integers or steps, but not the exclusion of any other element, integer or step, or group of elements, integers or steps.
The invention is hereinafter described with reference to the following non-limiting examples and accompanying figures. Brief description of the accompanying figures:
Figure 1 provides a gas chroma tograph trace (Trace A00445) of an extract of P. xjdostella pheromone glands. Trace A00444 is from an extract of other body tissues. Figure 2 provides graphical results for trap catches using Compositions
I and M described hereinafter.
Figure 3 provides graphical results for trap catches using Compositions J and L described hereinafter.
Example 1: Analysis of an extract of Plutella xylostella pheromone glands
As mentioned above, it was considered that it would be worth carrying out a new chemical analysis of the contents of the sex pheromone gland of Plutella xjdostella females using gas chromatography. The alternative approach of investigating the sensory sensilla in the males using electrophysiological techniques was rejected. Single cell studies rather than the simpler electroantennogram would be required for the necessary degree of compound selectivity to be achieved and the small size of the insect and the fragility of its antenna makes such an undertaking very difficult.
Koshihara and Yamada (1977) used an indirect method of collection in which a number of female insects were allowed to release the pheromone inside a glass flask. The pheromone deposited on the walls was then collected using a solvent. In the present instance, it was decided instead to excise pheromone glands from the females and extract the pheromone from the glands. Each method has advantages and disadvantages. The present choice was based on the fact that there was available methods for purifying the pheromone which removes most of the troublesome impurities. In addition, a method to discriminate between pheromone components and impurities using computer manipulated graphics to facilitate the comparison of GC traces was developed. Direct extraction from the glands also minimizes the oxidation and other decomposition of pheromone products which can occur by the indirect method. This was important because one of the components reported by Koshihara and Yamada (1977) is an aldehyde which is a relatively unstable compound.
After establishing a culture of the insect, a series of collections were carried out with varying numbers of glands, 10 to 30, pooled together to increase the amount of pheromone collected. Following extraction with hexane and removal of high boiling point components using an evaporative technique they were injected into a gas chromatograph containing a Polyethylene Glycol Column (SGE BP20). Extracts produced a consistent pattern of peaks, Trace A00445 on Figure 1. Their number was, however, rather high suggesting that not all of them were components of the pheromone. The pheromone glands in diamondback moth are very small and it is difficult to remove them without also including other body tissues. However, by comparing the GC traces with ones obtained from insect material from further up the abdomen, Trace A00444 on Figure 1. the peaks arising from other body tissues were eliminated. The traces indicated the presence of the two components identified by Tamaki et al.. marked as A and B on Figure 1. A third component. C. was also found which corresponds to one on the list found by Koshihara & Yamada (1980) to increase the numbers of insects caught in traps when it was added to the binary mixture, that is (Z)-ll-hexadecenol.
Example 2: Formulation of synthetic pheromone compositions and field trials
The identification in Example 1 of the third component (C) (ie. (Z)-ll- hexadecenol), does not in itself prove that it is a behaviourally active component of the P. xylostella pheromone. That is, it is possible that the third component was a precursor of one of the other components so that its presence might be coincidental. The best way of determining whether it actually contributes directly to the attraction is by a bioassay in which the old binary blend is compared with the new formulation containing the third component. Trapping of insects in an infested field using sticky traps baited with different pheromone compositions was considered the quickest and most effective method to resolve the matter.
Trial 1.
A four by four grid of traps, with 20m separation between them, was set up containing four different pheromone formulations in a Latin square distribution. The traps were constructed from waxed cardboard, measuring 85mm from base to apex and housed a replacable TanglefootE-coated liner, 90mm wide and 170mm long that was fixed to the base with a paper clip.
Baits consisted of 100 μg of pheromone dissolved in 10 μl of cyclohexane applied to the lumen of a 20mm length of surgical rubber tubing (internal diameter: 4.5mm. outer diameter: 6.5mm) placed centrally on the liner. Each trap contained the binary blend at two different ratios and two different formulations of a blend including (Z)-ll-hexadecenol. So as not to overwhelm the traps and to enhance any positive effect all the baits were made up with a concentration one tenth that normally used in commercial baits used for monitoring purposes. This was set up in a field of brussel sprouts in South Australia. The experiment was replicated three times using fresh baits. The numbers of insects caught at the different traps clearly showed that the formulations including (Z)-ll-hexadecenol was much more attractive to the insects than the old binary blend (Table 1).
Table 1.
Average numbers of insects caught over three weeks in 4 x 4 grid of traps, for each of the blends below arranged as a Latin square.
Figure imgf000007_0001
Composition (ratios) as follows:
Figure imgf000007_0002
Compositions C and D are more attractive than either A or B with a greater than 99.9% probability.
Trial 2.
In a second trial conducted in the same manner as Trial 1. "New Blend" formulation 2 (H) was more attractive than binary compositions of acetate/aldehyde and acetate/alcohol (see Table 2).
Table 2.
Figure imgf000008_0001
* Composition (ratios) as follows:
Figure imgf000008_0002
Trial 3.
A third trial was conducted at Lembang, Indonesia. There were five replicates of each of seven treatments, details of which are given in Table 3. Water traps were initially set out as shown in Table 4. with at least 20 m separation. Traps were rotated one position in a clockwise direction every ca 2 weeks. Compositions I-M were each loaded with a total of lOOOμg of pheromone onto red surgical rubber tubing. Composition N consisted of 100 μg of pheromone loaded on to grey rubber septa. The component proportions of these baits reflected the composition of virgin female pheromone glands as determined by Zilahibalogh et. al.. 1995. from a local Diamondback moth population. The compositions were not replaced during the trial.
Virgin females derived from a laboratory culture were placed individually in small cylinders with mesh-covered ends and were suspended from the underside of the lids covering the water traps. The protocol called for replacement of females when they died. Catches were recorded 2 to 3 times each week over the period of the trial (58 days).
Table 3. Ratio of components, Trial 3.
Figure imgf000009_0001
Table 4. Initial distribution of traps, Trial 3.
Figure imgf000009_0002
O - trap containing virgin females (non-synthetic control)
The greatest catch was achieved with Composition M. with which a total
1107 of moths was caught over the period of the trial (equivalent to 3.8 moths/trap/day) (Table 5). This composition comprised OAc:ALD:OH in a 1:1:0.4 ratio. In contrast, compositions with the same ratio of OAc:ALD but without OH (Composition I) resulted in a catch of 606 moths, or 2.1 moths/trap/day (Figure 2). When OH was added to a 2.5:7.5 ratio of ALD:OAc, the total catch increased from 287 (Composition J) to 896 (Composition L) (Figure 3).
Composition N performed poorly in comparison with all of the Compositions I-M. Although none of the latter had an ALD:OAc ratio corresponding exactly with that of N (6:4), Composition I was similar (ALD:OAc = 5 :5) but caught far more moths. Whilst differences in pheromone loading (1000 μg for Compositions I-M vs 100 μg for Composition N) may have contributed to the difference in bait efficacy in the long term, there was already a significant difference between the two baits after only eight days, where Compositions N and I averaged 2.2 and 4.6 moths/trap respectively.
Table 5. Raw data. Trial 3.
CATCH IN 5 TRAPS
Figure imgf000010_0001
Conclusion
The field trials have established that the pheromone contained in the sex pheromone glands of females of P. xjdostella is significantly different from the binary blend currently used for monitoring. Compositions including (Z)-ll-hexadecenol out performs the old binary compositions by a factor of 4-10 as measured by the number of insects which are attracted into a trap.
References
Chisholm M.D., Steck, W.F., Underhill, E.W. & Palaniswamy, P. (1982) Field trapping of diamondback moth Plutella xylostella using an improved four- component sex attractant blend. J. Chem. Ecol. 9. 113-118.
Koshihara. T. & Yamada. H. (1980). Attractant activity of the female sex pheromone of diamondback moth, Plutella xylostella, (L.), and analogue. Jap. J. Appl. Ento. Zool. 24, 6-12.
Tamaki. Y., Kawasaki. K., Yamada, H., Koshihara, T.. Osaki, N.. Ando, T.. Yoshida. S. & Kakinohana, H. (1977). Z-11-Hexadecenal and Z-ll- hexadecenyl acetate: Sex pheromone components of the diamondback moth (Lepidoptera: Plutellidae). Appl. Ent. Zool, 12, 108-210.
Zilahibalogh G.M.G., Angerilli N.P.D., Borden J.H., Meray M., Tulung M. and Sembel D. (1995). Regional differences in pheromone responses of diamondback moth in Indonesia. International Journal of Pest Managment 41, 201-204.
It will be appreciated by persons skilled in the art that numerous variations and/or modifications may be made to the invention as shown in the specific embodiments without departing from the spirit or scope of the invention as broadly described. The present embodiments are, therefore, to be considered in all respects as illustrative and not restrictive.

Claims

Claims:
1. A synthetic pheromone composition comprising (Z)-ll-hexadecenyl acetate, (Z)-ll-hexadecenal and (Z)-ll-hexadecenol and, optionally, a i suitable solvent.
2. A synthetic pheromone composition according to claim 1 having a (Z)- 11-hexadecenyl acetate:(Z)-ll-hexadecenal:(Z)-ll-hexadecenol component weight/weight ratio of 10:2-25:1-10.
3. A synthetic pheromone composition according to claim 1 having a (Z)- 11-hexadecenyl acetate: (Z)-ll-hexadecenal:(Z)-ll-hexadecenol component weight/weight ratio of 10:10:4.
4. A method of trapping diamondback moths comprising the step of providing an infested area with one or more insect traps containing an amount of a composition of any one of the preceding claims.
5. A method according to claim 4, wherein said amount is about 50-2000 μg/trap.
6. The method according to claim 4, wherein said amount is about 100- 1000 μg/trap.
7. A synthetic pheromone composition according to any one of claims 1 to 3. further comprising a suitable insecticide.
8. A method of controlling the proliferation of diamondback moths comprising the step of dispensing within an infested area an amount of a composition according to any one of claims 1 to 3 or 7 which is sufficient to disrupt diamondback moth mating.
9. A method according to claim 8, wherein the composition is dispensed at a rate of about 10-lOOmg/ha/hour.
PCT/AU2000/001417 1999-11-22 2000-11-21 Diamondback moth pheromone composition WO2001037664A1 (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
AU15041/01A AU1504101A (en) 1999-11-22 2000-11-21 Diamondback moth pheromone composition

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
AUPQ4172 1999-11-22
AUPQ4172A AUPQ417299A0 (en) 1999-11-22 1999-11-22 Diamond back moth pheromone composition

Publications (1)

Publication Number Publication Date
WO2001037664A1 true WO2001037664A1 (en) 2001-05-31

Family

ID=3818316

Family Applications (1)

Application Number Title Priority Date Filing Date
PCT/AU2000/001417 WO2001037664A1 (en) 1999-11-22 2000-11-21 Diamondback moth pheromone composition

Country Status (2)

Country Link
AU (2) AUPQ417299A0 (en)
WO (1) WO2001037664A1 (en)

Citations (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
AU4207278A (en) * 1977-12-01 1979-06-07 Hoechst Ag Insect attractant
US4575458A (en) * 1982-09-29 1986-03-11 Canadian Patents And Development Limited Multicomponent attractant for armyworm moths
AU4326793A (en) * 1992-06-18 1994-01-04 Ncsr "Demokritos" Inclusion complexes of cyclodextrin and their use in slow release formulations for attracting insects

Patent Citations (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
AU4207278A (en) * 1977-12-01 1979-06-07 Hoechst Ag Insect attractant
US4575458A (en) * 1982-09-29 1986-03-11 Canadian Patents And Development Limited Multicomponent attractant for armyworm moths
AU4326793A (en) * 1992-06-18 1994-01-04 Ncsr "Demokritos" Inclusion complexes of cyclodextrin and their use in slow release formulations for attracting insects

Non-Patent Citations (13)

* Cited by examiner, † Cited by third party
Title
ANTO T. ET AL.: "Electroantennogram activities of sex pheromone analogues and their synergistic effect on field attraction in the diamondback moth", APPL. ENT. ZOOL., vol. 14, no. 3, 1979, pages 362 - 364 *
CHISHOLM M.D. ET AL.: "Field trapping of diamondback moth plutella xylostella using an improved four-component sex attractant blend", JOURNAL OF CHEMICAL ECOLOGY, vol. 9, no. 1, 1983, pages 113 - 118 *
DATABASE CAPLUS [online] KANG S.K. ET AL., accession no. STN Database accession no. 1988:528630 *
DATABASE CAPLUS [online] KANG S.K., accession no. STN Database accession no. 1990:477665 *
DATABASE CAPLUS [online] KOSHIHARA T. AND YAMADA H., accession no. STN Database accession no. 1980:564806 *
DATABASE CAPLUS [online] LIN Y.M. AND CHOW Y.S.: "Chung yang yen chiu yuan chih wu yen chiu so chuan k'an", XP002941524, accession no. STN Database accession no. 1984:63484 *
LANDOLT P.J. AND SN-IITHHISLER C.L.: "Isolation and identification of female sex pheremone a sex attractant for laconobia subjuncta", JOURNAL OF CHEMICAL ECOLOGY, vol. 24, no. 8, 1998, pages 1369 - 1379 *
LIN Y. ET AL.: "Field trapping of the diamondback moth plutella xylostella (linnaues) and pseudaletia separata walker using the synthetic sex pheromone of the diamondback moth", BULL. INST. ZOOL., ACADEMIA SINICA, vol. 21, no. 2, 1982, pages 121 - 127 *
LIN Y. ET AL.: "The distance effects of (Z)-9-tetradecenyl acetate and (Z)- 1 1 -hexadecen-1 -01 on the sexual communication of diamondback moth plutella xylostella L", BULL. INST. ZOOL., ACADEMIA SINICA, vol. 23, no. 2, 1984, pages 187 - 192 *
NIPPON OYO DOBUTSU KONCHU GAKKAISHI, vol. 24, no. 1, 1980, JAPANESE, pages 6 - 12 *
PROC. SEMIN. ALLELOCHEM. PHEROMONES, 1982, pages 147 - 155 *
TACHAN HWAHAKHOE CHI, vol. 32, no. 1, 1988, KOREAN, pages 60 - 64 *
TACHAN HWAHAKHOE CHI, vol. 34, no. 2, 1990, KOREAN, pages 179 - 183 *

Also Published As

Publication number Publication date
AUPQ417299A0 (en) 1999-12-16
AU1504101A (en) 2001-06-04

Similar Documents

Publication Publication Date Title
Tan et al. Mutual reproductive benefits between a wild orchid, Bulbophyllum patens, and Bactrocera fruit flies via a floral synomone
Krasnoff et al. Dihydropyrrolizine attractants for arctiid moths that visit plants containing pyrrolizidine alkaloids
Hieu et al. Behavioural and electroantennogram responses of the stable fly (Stomoxys calcitrans L.) to plant essential oils and their mixtures with attractants
Navarro-Llopis et al. Response of two tephritid species, Bactrocera oleae and Ceratitis capitata, to different emission levels of pheromone and parapheromone
Smart et al. Effect of visual cues and a mixture of isothiocyanates on trap capture of cabbage seed weevil, Ceutorhynchus assimilis
Molnár et al. Development of a female-targeted lure for the box tree moth Cydalima perspectalis (Lepidoptera: Crambidae): A preliminary report
Zhang et al. Male-produced anti-sex pheromone in a plant bug
Mendel et al. Outdoor attractancy of males of Matsucoccus josephi (Homoptera: Matsucoccidae) and Elatophilus hebraicus (Hemiptera: Anthocoridae) to synthetic female sex pheromone of Matsucoccus josephi
Riba et al. Pheromone response inhibitors of the corn stalk borer Sesamia nonagrioides. Biological evaluation and toxicology
WO1998007316A1 (en) A novel trapping system for mediterranean fruit flies
EP2572579B1 (en) Compositions for attracting Tortricidae (fruit moths)
US6562332B2 (en) Attractants of beneficial insects
Rojas et al. Identification of the sex pheromone of Copitarsia decolora (Lepidoptera: Noctuidae)
JPS61268602A (en) Novel composition and method for controlling cockroach
WO2001037664A1 (en) Diamondback moth pheromone composition
US5002971A (en) Method and agent for controlling the peach twig borer
US6413508B1 (en) Green leaf volatiles as synergists for insect pheromones
US20180206489A1 (en) Repellent effective against anopheles gambiae
Tatsuki et al. Disruption of sex pheromone communication in Chilo suppressalis with pheromone and analogs
Leonhardt et al. Comparison of ceralure and trimedlure attractants for the male Mediterranean fruit fly (Diptera: Tephritidae)
Sternlicht et al. Field evaluation of the synthetic female sex pheromone of the citrus flower moth, Prays citri (Mill.)(Lepidoptera: Yponomeutidae), and related compounds
Zhang et al. Electrophysiological and behavioral responses of Dendroctonus valens to non-host volatiles
Kim et al. Simultaneous mating disruption of two Grapholita species in apple orchards
Bedard et al. Cydia strobilella (Lepidoptera: Tortricidae): antennal and behavioral responses to host and nonhost volatiles
Bradshaw et al. A novel autostimulatory pheromone regulating transport of leaves in Atta cephalotes

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 BR BY BZ CA CH CN CR CU CZ DE DK DM DZ 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 PL PT RO RU SD SE SG SI SK SL TJ TM TR TT TZ UA UG US UZ VN YU ZA 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 TZ UG ZW AM AZ BY KG KZ MD RU TJ TM AT BE CH CY DE DK ES FI FR GB GR IE IT LU MC NL PT SE TR BF BJ CF CG CI CM GA GN 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: 15041/01

Country of ref document: AU

REG Reference to national code

Ref country code: DE

Ref legal event code: 8642

122 Ep: pct application non-entry in european phase