JP2012229196A - Attractant of nezara antennata - Google Patents

Attractant of nezara antennata Download PDF

Info

Publication number
JP2012229196A
JP2012229196A JP2012020647A JP2012020647A JP2012229196A JP 2012229196 A JP2012229196 A JP 2012229196A JP 2012020647 A JP2012020647 A JP 2012020647A JP 2012020647 A JP2012020647 A JP 2012020647A JP 2012229196 A JP2012229196 A JP 2012229196A
Authority
JP
Japan
Prior art keywords
attractant
epoxy
bisabolen
control
trans
Prior art date
Legal status (The legal status 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 status listed.)
Granted
Application number
JP2012020647A
Other languages
Japanese (ja)
Other versions
JP5891546B2 (en
Inventor
Nobuyuki Endo
信幸 遠藤
Yukiyoshi Muto
進悦 武藤
Rikiya Sasaki
力也 佐々木
Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)
Fuji Flavor Co Ltd
National Agriculture and Food Research Organization
Original Assignee
Fuji Flavor Co Ltd
National Agriculture and Food Research Organization
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 Fuji Flavor Co Ltd, National Agriculture and Food Research Organization filed Critical Fuji Flavor Co Ltd
Priority to JP2012020647A priority Critical patent/JP5891546B2/en
Publication of JP2012229196A publication Critical patent/JP2012229196A/en
Application granted granted Critical
Publication of JP5891546B2 publication Critical patent/JP5891546B2/en
Active legal-status Critical Current
Anticipated expiration legal-status Critical

Links

Landscapes

  • Agricultural Chemicals And Associated Chemicals (AREA)

Abstract

PROBLEM TO BE SOLVED: To provide an attractant which is utilized as an attraction source for grasping easily an vermination density or the time of vermination of Nezara antennata on an agriculture field or the like, and has a practically sufficient attraction effect against the Nezara antennata.SOLUTION: This attractant of the Nezara antennata includes cis-1,2-epoxy-(Z)-α-bisabolene and trans-1,2-epoxy-(Z)-α-bisabolene as main components, wherein the content of the trans-1,2-epoxy-(Z)-α-bisabolene is larger than the content of the cis-1,2-epoxy-(Z)-α-bisabolene.

Description

本発明はアオクサカメムシの誘引剤に関する。   The present invention relates to an attractant for Aoksakamemushi.

カメムシ目カメムシ科に属するアオクサカメムシ(学名:Nezara antennata)は、日本をはじめ、亜熱帯アジアに広く生息し、イネ科やマメ科さらには果菜類など25科80種を加害する広食性の害虫であり、日本において、アオクサカメムシは、大豆や水稲、果樹類に大きな被害をもたらしている。
従来の発生予察を行うための一般的な手段としては、目視による見取り調査や捕虫網を使ったすくい取り調査等が行われてきたが、これらの方法は多大な労力を必要とする他、調査者の経験により結果が左右されるという問題点を持つ。
一方、フェロモン等の誘引剤を利用したトラップでは、対象害虫のみを選択的に捕獲できることや調査経験などの人為的な影響を排除できるため、発生予察を効率的に行うことができる。
以上のことから、アオクサカメムシを対象とした発生予察においても、誘引効果の高い誘引剤の開発およびその利用が望まれている。
Aoksakamamemushi (Scientific name: Nezara antennata) is a widespread pest that inhabits widely in subtropical Asia, including Japan, and injures 80 species of 25 families such as gramineae, legumes and fruit vegetables. And in Japan, Aoksamememushi causes great damage to soybeans, paddy rice and fruit trees.
Conventional methods for predicting outbreaks include visual inspections and scooping surveys using insect nets, but these methods require a great deal of labor, and investigators There is a problem that the result depends on the experience.
On the other hand, in traps using attractants such as pheromones, it is possible to selectively capture only the target pests and to eliminate artificial influences such as research experience, so that occurrence prediction can be performed efficiently.
From the above, the development and use of attractants with a high attracting effect are also desired in the prediction of outbreaks targeting blue sea bugs.

従来、アオクサカメムシに対し誘引効果のある成分は、知られておらず、発生予察などに誘引物質が利用されていない。   Conventionally, ingredients that have an attracting effect on blue-tailed bugs are not known, and no attracting substances are used for predicting outbreaks.

なお、アオクサカメムシの近縁種であるミナミアオカメムシ(学名:Nezara viridula)は、熱帯原産で世界各地に分布し、32科145種の植物への加害が確認されている。
該ミナミアオカメムシのフェロモンについては、(Z)−α−ビザボレン、シス−1,2−エポキシ−(Z)−α−ビザボレン、トランス−1,2−エポキシ−(Z)−α−ビザボレン、(E)−ネロリドール、n−ノナデカンの5成分で構成されていることが明らかとなっている(Journal of Experimental Zoology、第244巻、第1号、171−175、1987年、 Naturwissenschaften、76巻、173−175、1989年、Journal of Chemical Ecology、第20巻、第12号、3133−3147、1994年)。
In addition, the southern blue stink bug (Scientific name: Nezara viridula), which is a related species of the blue stink bug, is native to the tropics and is distributed around the world, and it has been confirmed that it damages 145 species of 32 families.
The pheromones of the southern blue stink bug are (Z) -α-bisabolen, cis-1,2-epoxy- (Z) -α-bisabolen, trans-1,2-epoxy- (Z) -α-bisabolen, ( E) -nerolidol, n-nonadecane, it has been revealed that it is composed of five components (Journal of Experimental Zoology, Vol. 244, No. 1, 171-175, 1987, Naturewissenchaften, Vol. 76, 173-175, 1989, Journal of Chemical Ecology, Vol. 20, No. 12, 3133-3147, 1994).

従って、本発明の課題は、農業現場等において、アオクサカメムシの発生密度や発生時期を簡易に把握するための誘引源として利用でき、アオクサカメムシに対して実用的に充分な誘引効果を有する誘引剤を提供することにある。   Therefore, the problem of the present invention is that it can be used as an inducement source for easily grasping the occurrence density and occurrence time of blue-tailed beetles at an agricultural site and the like, and has a practically sufficient attracting effect against blue-tailed bugs. To provide an attractant.

本発明者らは、上記課題を解決すべく鋭意検討し、アオクサカメムシに対し顕著な誘引活性を示す成分を見出した。   The present inventors diligently studied to solve the above-mentioned problems, and found a component exhibiting a remarkable attracting activity against the blue bug.

すなわち、シス−1,2−エポキシ−(Z)−α−ビザボレンおよび、トランス−1,2−エポキシ−(Z)−α−ビザボレンの2成分を主成分とし、この2成分の含有量について、トランス−1,2−エポキシ−(Z)−α−ビザボレンの含有量が、シス−1,2−エポキシ−(Z)−α−ビザボレンの含有量以上である誘引剤は、アオクサカメムシの雌雄成虫に対して有効な誘引性を示すことを見出し、本発明を完成するに至った。   That is, two components of cis-1,2-epoxy- (Z) -α-bisabolen and trans-1,2-epoxy- (Z) -α-bisabolene are the main components, and the content of these two components is The attractant in which the content of trans-1,2-epoxy- (Z) -α-bisabolen is greater than or equal to the content of cis-1,2-epoxy- (Z) -α-bisabolen is male and female The present inventors have found that the present invention exhibits effective attractiveness against adults, and have completed the present invention.

この2成分の含有量は、シス−1,2−エポキシ−(Z)−α−ビザボレンの含有量を10とすると、トランス−1,2−エポキシ−(Z)−α−ビザボレンの含有量が45〜55であることが好ましい。   The content of these two components is such that when the content of cis-1,2-epoxy- (Z) -α-bisabolen is 10, the content of trans-1,2-epoxy- (Z) -α-bisabolen is It is preferable that it is 45-55.

本発明に係る誘引剤の調製は、これらの物質を用いて、通常、誘引剤の調製に際して適用されている製剤化技術を用いて行うことができる。
例えば、2成分を混合した化合物を、そのまま、あるいはエーテル、アセトン、アルコール、ヘキサン、ペンタン、ジクロロメタン、トリグリセライド等の適当な溶媒で希釈した後、適当な担体、例えば、各種合成高分子体、ゴム等に吸着させたり、綿や不織布、紙、繊維等に含浸させたり、さらに適当な高分子材料の成型物に封入することで製剤化することができる。
The attractant according to the present invention can be prepared by using these substances and by using a formulation technique which is usually applied in the preparation of the attractant.
For example, the compound obtained by mixing the two components is used as it is or after being diluted with an appropriate solvent such as ether, acetone, alcohol, hexane, pentane, dichloromethane, triglyceride, etc., and then an appropriate carrier such as various synthetic polymers, rubber, etc. It can be made into a preparation by adsorbing it on the surface, impregnating it with cotton, non-woven fabric, paper, fiber or the like, or encapsulating it in a molded product of an appropriate polymer material.

有効成分の含有量は、使用環境に応じて適宜定めることができるが、通常製剤あたりの有効成分量が1mg〜10g、好ましくは10mg〜500mgの範囲になるように添加する。   The content of the active ingredient can be appropriately determined according to the use environment, but it is usually added so that the amount of the active ingredient per preparation is in the range of 1 mg to 10 g, preferably 10 mg to 500 mg.

本発明の誘引剤は、水盤式、滑落式、粘着式等の任意の形態の捕虫器の誘引源として利用することができる。   The attractant of the present invention can be used as an attracting source for any form of insect trap such as laver type, sliding-down type, and adhesive type.

本発明によれば、アオクサカメムシに対して実用的に充分な誘引効果を有する誘引剤を提供することができる。   ADVANTAGE OF THE INVENTION According to this invention, the attractant which has a practically sufficient attraction effect can be provided with respect to the blue beetle.

以下に実施例を用いて本発明を詳細に説明するが、本発明はこれに限定されるものではない。   Hereinafter, the present invention will be described in detail using examples, but the present invention is not limited thereto.

(実施例1)
本発明誘引剤1は、20mgのシス−1,2−エポキシ−(Z)−α−ビザボレンと20mgのトランス−1,2−エポキシ−(Z)−α−ビザボレンとを混合し、合成高分子体(ポリエチレンと酢酸ビニルの共重合)に吸着させることで製剤化したものである。
Example 1
The attractant 1 of the present invention is a synthetic polymer prepared by mixing 20 mg of cis-1,2-epoxy- (Z) -α-bisaborane and 20 mg of trans-1,2-epoxy- (Z) -α-bisabolen. It is formulated by adsorbing to the body (copolymerization of polyethylene and vinyl acetate).

対照誘引剤1は、20mgのトランス−1,2−エポキシ−(Z)−α−ビザボレンを単独で用い、合成高分子体(ポリエチレンと酢酸ビニルの共重合)に吸着させることで製剤化したものである。
対照誘引剤2は、20mgのシス−1,2−エポキシ−(Z)−α−ビザボレンを単独で用い、合成高分子体に吸着させることで製剤化したものである。
対照誘引剤3は、20mgの(Z)−α−ビザボレンを単独で用い、合成高分子体に吸着させることで製剤化したものである。
対照誘引剤4は、20mgの(Z)−α−ビザボレンと、20mgのトランス−1,2−エポキシ−(Z)−α−ビザボレンとを混合し、合成高分子体に吸着させることで製剤化したものである。
対照誘引剤5は、20mgの(Z)−α−ビザボレンと、20mgのシス−1,2−エポキシ−(Z)−α−ビザボレンとを混合し、合成高分子体に吸着させることで製剤化したものである。
対照誘引剤6は、20mgの(Z)−α−ビザボレンと、20mgのシス−1,2−エポキシ−(Z)−α−ビザボレンと、20mgのトランス−1,2−エポキシ−(Z)−α−ビザボレンとを混合し、合成高分子体に吸着させることで製剤化したものである。
Control attractant 1 was formulated by using 20 mg of trans-1,2-epoxy- (Z) -α-bisabolen alone and adsorbing it to a synthetic polymer (copolymerization of polyethylene and vinyl acetate). It is.
Control attractant 2 was formulated by adsorbing 20 mg of cis-1,2-epoxy- (Z) -α-bisabolen alone to a synthetic polymer.
Control attractant 3 was formulated by adsorbing 20 mg of (Z) -α-bizaborane alone to a synthetic polymer.
Control attractant 4 is formulated by mixing 20 mg of (Z) -α-bisaborane and 20 mg of trans-1,2-epoxy- (Z) -α-bisabolen and adsorbing them to a synthetic polymer. It is a thing.
Control attractant 5 is formulated by mixing 20 mg of (Z) -α-bisaborane and 20 mg of cis-1,2-epoxy- (Z) -α-bisabolen and adsorbing them to a synthetic polymer. It is a thing.
Control attractant 6 consists of 20 mg of (Z) -α-bisabolen, 20 mg of cis-1,2-epoxy- (Z) -α-bisabolen and 20 mg of trans-1,2-epoxy- (Z)- It is formulated by mixing with α-bisabolen and adsorbing to a synthetic polymer.

対照誘引剤7は、何の物質も吸着させていない合成高分子体(ポリエチレンと酢酸ビニルの共重合)を、対照のために準備したものである。   The control attractant 7 is a synthetic polymer (copolymer of polyethylene and vinyl acetate) that has not adsorbed any substance, prepared for control.

次に、上記で得た本発明誘引剤1及び対照誘引剤1〜7について、各誘引剤の誘引効果を確認するために行った試験について説明する。   Next, the test performed in order to confirm the attracting effect of each attractant about this invention attractant 1 and the control attractants 1-7 obtained above is demonstrated.

各試験は、上記で得た各誘引剤を、各トラップに装着したものを用意し、同一条件下で、各トラップを設置し、アオクサカメムシの捕虫数を調査することで行った。
ここで、捕虫結果は、対照誘引剤1(トランス−1,2−エポキシ−(Z)−α−ビザボレン単独)の捕虫数を100として、他の誘引剤の捕虫数を、対照誘引剤1に対する捕虫比として表した。
その結果は、次のとおりである。
Each test was carried out by preparing each attractant obtained above in each trap, setting each trap under the same conditions, and investigating the number of insects captured by the blue bug.
Here, the insect trapping results are as follows: the trapping number of the control attractant 1 (trans-1,2-epoxy- (Z) -α-bisabolen alone) is 100, and the trapping number of the other attractant is compared to the control attractant 1. Expressed as catch ratio.
The results are as follows.

本発明誘引剤1は357、対照誘引剤1は100(基準)、対照誘引剤2は29、対照誘引剤3は14、対照誘引剤4は157、対照誘引剤5は143、対照誘引剤6は214、対照誘引剤7は0であった。   The present invention attractant 1 is 357, control attractant 1 is 100 (reference), control attractant 2 is 29, control attractant 3 is 14, control attractant 4 is 157, control attractant 5 is 143, control attractant 6 214 and control attractant 7 was 0.

上記の結果に示すように、本発明誘引剤1は、単独成分による対照誘引剤1〜3及び3成分の対照誘引剤6より強い捕虫効果を有し、実用的に充分な誘引効果を有することが確認できる。   As shown in the above results, the attractant 1 of the present invention has a stronger insect trapping effect than the control attractants 1 to 3 of the single component and the control attractant 6 of the three components, and has a practically sufficient attracting effect. Can be confirmed.

(実施例2)
本発明誘引剤2は、10mgのシス−1,2−エポキシ−(Z)−α−ビザボレンと50mgのトランス−1,2−エポキシ−(Z)−α−ビザボレンとを混合し、合成高分子体(ポリエチレンと酢酸ビニルの共重合)に吸着させることで製剤化したものである。
本発明誘引剤3は、30mgのシス−1,2−エポキシ−(Z)−α−ビザボレンと30mgのトランス−1,2−エポキシ−(Z)−α−ビザボレンとを混合し、合成高分子体に吸着させることで製剤化したものである。
(Example 2)
The attractant 2 of the present invention is a synthetic polymer prepared by mixing 10 mg of cis-1,2-epoxy- (Z) -α-bisaborane and 50 mg of trans-1,2-epoxy- (Z) -α-bisabolen. It is formulated by adsorbing to the body (copolymerization of polyethylene and vinyl acetate).
The attractant 3 of the present invention is a synthetic polymer prepared by mixing 30 mg of cis-1,2-epoxy- (Z) -α-bisaborane and 30 mg of trans-1,2-epoxy- (Z) -α-bisabolen. It is formulated by adsorbing to the body.

対照誘引剤8は、60mgのトランス−1,2−エポキシ−(Z)−α−ビザボレンを単独で用い、合成高分子体(ポリエチレンと酢酸ビニルの共重合)に吸着させることで製剤化したものである。
対照誘引剤9は、60mgのシス−1,2−エポキシ−(Z)−α−ビザボレンを単独で用い、合成高分子体に吸着させることで製剤化したものである。
対照誘引剤10は、50mgのシス−1,2−エポキシ−(Z)−α−ビザボレンと、10mgのトランス−1,2−エポキシ−(Z)−α−ビザボレンとを混合し、合成高分子体に吸着させることで製剤化したものである。
Control attractant 8 was formulated by adsorbing 60 mg of trans-1,2-epoxy- (Z) -α-bisabolen alone to a synthetic polymer (copolymer of polyethylene and vinyl acetate). It is.
Control attractant 9 was formulated by adsorbing 60 mg of cis-1,2-epoxy- (Z) -α-bisabolen alone to a synthetic polymer.
The control attractant 10 was prepared by mixing 50 mg of cis-1,2-epoxy- (Z) -α-bisabolene with 10 mg of trans-1,2-epoxy- (Z) -α-bisabolen. It is formulated by adsorbing to the body.

対照誘引剤11は、何の物質も吸着させていない合成高分子体(ポリエチレンと酢酸ビニルの共重合)を、対照のために準備したものである。   The control attractant 11 is a synthetic polymer (copolymer of polyethylene and vinyl acetate) that has not adsorbed any substance, prepared for control.

次に、上記で得た本発明誘引剤2、3及び対照誘引剤8〜11について、各誘引剤の誘引効果を確認するために行った試験について説明する。   Next, tests conducted to confirm the attracting effect of each attractant for the present attractants 2, 3 and control attractants 8 to 11 obtained above will be described.

各試験は、上記で得た各誘引剤を、各トラップに装着したものを用意し、同一条件下で、各トラップを設置し、アオクサカメムシ及びアオクサカメムシの近縁種であるミナミアオカメムシの捕虫数を調査することで行った。
ここで、捕虫結果は、アオクサカメムシにおける対照誘引剤8(トランス−1,2−エポキシ−(Z)−α−ビザボレン単独)の捕虫数を100として、他の誘引剤の捕虫数を、アオクサカメムシにおける対照誘引剤8に対する捕虫比として表した。
その結果は、次のとおりである。
For each test, prepare each attractant obtained above in each trap, and install each trap under the same conditions. It was done by investigating the number of insects.
Here, the insect trapping results are as follows: the trapping number of the control attractant 8 (trans-1,2-epoxy- (Z) -α-bisabolen alone) in the blue beetle is 100, and the trapping number of other attractants is It was expressed as the ratio of catching insects to the control attractant 8 in laceworm.
The results are as follows.

アオクサカメムシについて、本発明誘引剤2は139、本発明誘引剤3は121、対照誘引剤8は100(基準)、対照誘引剤9は54、対照誘引剤10は94、対照誘引剤11は3であった。
また、ミナミアオカメムシについて、本発明誘引剤2は18、本発明誘引剤3は18、対照誘引剤8は0、対照誘引剤9は3、対照誘引剤10は38、対照誘引剤11は0であった。
For the blue bug, attractant 2 of the present invention is 139, attractant 3 of the present invention is 121, control attractant 8 is 100 (reference), control attractant 9 is 54, control attractant 10 is 94, and control attractant 11 is 3.
In addition, for the southern blue stink bug, the present attractant 2 is 18, the present attractant 3 is 18, the control attractant 8 is 0, the control attractant 9 is 3, the control attractant 10 is 38, and the control attractant 11 is 0. Met.

上記の結果に示すように、本発明誘引剤2、3は、アオクサカメムシについて、単独成分による対照誘引剤8、9及び対照誘引剤10(トランス−1,2−エポキシ−(Z)−α−ビザボレンに対してシス−1,2−エポキシ−(Z)−α−ビザボレンの含有量が多いタイプ)より強い捕虫効果を有し、実用的に充分な誘引効果を有することが確認できる。
また、ミナミアオカメムシについては、対照誘引剤10(トランス−1,2−エポキシ−(Z)−α−ビザボレンに対してシス−1,2−エポキシ−(Z)−α−ビザボレンの含有量が多いタイプ)が強い捕虫効果を有していること、及び対照誘引剤8(トランス−1,2−エポキシ−(Z)−α−ビザボレン単独)の誘引効果が全くなかったことが確認できる。
このことから、アオクサカメムシとミナミアオカメムシは、近縁種であっても有効な誘引物質が異なることがわかる。
As shown in the above results, the attractants 2 and 3 of the present invention are the control attractants 8 and 9 and the control attractant 10 (trans-1,2-epoxy- (Z) -α by a single component) with respect to the blue bug. It can be confirmed that it has a stronger insect trapping effect than a type with a high content of cis-1,2-epoxy- (Z) -α-bisabolen) with respect to visaborene, and has a practically sufficient attracting effect.
In addition, for the southern blue stink bug, the content of cis-1,2-epoxy- (Z) -α-bisabolen relative to the control attractant 10 (trans-1,2-epoxy- (Z) -α-bisabolene) It can be confirmed that many types) had a strong insect trapping effect and that there was no attracting effect of the control attractant 8 (trans-1,2-epoxy- (Z) -α-bisabolen alone).
From this, it can be seen that the effective attractant differs between Aoxus stink bug and Southern blue stink bug even if they are closely related species.

Journal of Experimental Zoology、第244巻、第1号、171−175、1987年Journal of Experimental Zoology, Vol. 244, No. 1, 171-175, 1987 Naturwissenschaften、76巻、173−175、1989年Naturwissenschaften, 76, 173-175, 1989 Journal of Chemical Ecology、第20巻、第12号、3133−3147、1994年Journal of Chemical Ecology, Vol. 20, No. 12, 3133-3147, 1994

Claims (2)

シス−1,2−エポキシ−(Z)−α−ビザボレンと、トランス−1,2−エポキシ−(Z)−α−ビザボレンとを主成分とし、この2成分の含有量について、トランス−1,2−エポキシ−(Z)−α−ビザボレンの含有量が、シス−1,2−エポキシ−(Z)−α−ビザボレンの含有量以上であることを特徴とする、アオクサカメムシの誘引剤。   The main component is cis-1,2-epoxy- (Z) -α-bisabolen and trans-1,2-epoxy- (Z) -α-bisabolen. The content of these two components is trans-1, The attractant for the blue bug, characterized in that the content of 2-epoxy- (Z) -α-bisabolen is greater than or equal to the content of cis-1,2-epoxy- (Z) -α-bisabolen. シス−1,2−エポキシ−(Z)−α−ビザボレンと、トランス−1,2−エポキシ−(Z)−α−ビザボレンとを主成分とし、シス−1,2−エポキシ−(Z)−α−ビザボレンの含有量を10とすると、トランス−1,2−エポキシ−(Z)−α−ビザボレンの含有量が45〜55であることを特徴とする、アオクサカメムシの誘引剤。     The main component is cis-1,2-epoxy- (Z) -α-bisabolen and trans-1,2-epoxy- (Z) -α-bisabolen, and cis-1,2-epoxy- (Z)- An attractant for the blue bug, characterized in that the content of trans-1,2-epoxy- (Z) -α-bisabolen is 45 to 55 when the content of α-bisabolen is 10.
JP2012020647A 2011-04-11 2012-02-02 Aoxus stink bug attractant Active JP5891546B2 (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP2012020647A JP5891546B2 (en) 2011-04-11 2012-02-02 Aoxus stink bug attractant

Applications Claiming Priority (3)

Application Number Priority Date Filing Date Title
JP2011086978 2011-04-11
JP2011086978 2011-04-11
JP2012020647A JP5891546B2 (en) 2011-04-11 2012-02-02 Aoxus stink bug attractant

Publications (2)

Publication Number Publication Date
JP2012229196A true JP2012229196A (en) 2012-11-22
JP5891546B2 JP5891546B2 (en) 2016-03-23

Family

ID=47431095

Family Applications (1)

Application Number Title Priority Date Filing Date
JP2012020647A Active JP5891546B2 (en) 2011-04-11 2012-02-02 Aoxus stink bug attractant

Country Status (1)

Country Link
JP (1) JP5891546B2 (en)

Citations (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US4981981A (en) * 1988-03-14 1991-01-01 The United States Of America As Represented By The Secretary Of Agriculture Sesquiterpene epoxides and process for their preparation
JPH0570449A (en) * 1991-09-12 1993-03-23 Sumitomo Chem Co Ltd Production of sex pheromen of stinkbugs belonging to nezara and acrosternum species

Patent Citations (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US4981981A (en) * 1988-03-14 1991-01-01 The United States Of America As Represented By The Secretary Of Agriculture Sesquiterpene epoxides and process for their preparation
JPH0570449A (en) * 1991-09-12 1993-03-23 Sumitomo Chem Co Ltd Production of sex pheromen of stinkbugs belonging to nezara and acrosternum species

Non-Patent Citations (1)

* Cited by examiner, † Cited by third party
Title
JPN6015041076; Zeitschrift fuer Naturforschung, C: Journal of Biosciences (1993) 48c, 1993, 73-79 *

Also Published As

Publication number Publication date
JP5891546B2 (en) 2016-03-23

Similar Documents

Publication Publication Date Title
CN101627757B (en) Dark melolonthidae sex pheromone and sex attractant
Brandes et al. Pyrethroid resistance of insect pests of oilseed rape in Germany
Vargas et al. Attraction and mortality of Bactrocera dorsalis (Diptera: Tephritidae) to STATIC spinosad ME weathered under operational conditions in California and Florida: A reduced-risk male annihilation treatment
CN105379711A (en) Monochamus alternatus trapping and killing viscose glue
KR20150039512A (en) Multi-species attraction of stink bugs with pheromone compounds complex and its trap
CN115426882A (en) New sex pheromone component for fall armyworm and spodoptera frugiperda
CN105053020A (en) Application of H.beicherriana in preventing and treating lissorhoptrus oryzophilus kuschel
Farooq et al. Comparative efficacy of different pesticide residue mitigation modules in mango
JP5891546B2 (en) Aoxus stink bug attractant
KR101468450B1 (en) Non woven fabric-type pheromone dispenser for controlling harmful insect and uses thereof
Singh et al. Population suppression of fruit flies (Bactrocera spp.) in mango (Mangifera indica) orchards
Sreelakshmi et al. Management of resistant populations of legume pod borer, Maruca vitrata Fabricius (Lepidoptera: Crambidae) using new generation insecticides
KR101593002B1 (en) Murgantiol as a stink bug synergistic attractant for use outdoors
Rahmouni et al. Efficiency of Cryptolaemus montrouzieri Mulsant (Coleoptera: Coccinellidae) to control Planococcus citri Risso (Hemiptera: Pseudococcidae) in citrus orchards in Tunisia
Saipollizan et al. Laboratory efficacy and toxicology of two commercial insecticides (deltamethrin and fenitrothion) against two German cockroach field strains
JP2009051763A (en) Attractant of unibanded stink bug
Khan et al. Control of rodent damage to groundnuts in the Pothwar plateau region of Pakistan
Nortjé et al. The successes of stinkbug research and the Stinkbug Working Group in the Southern African avocado and macadamia industries
JP7542364B2 (en) Attractant for sawtooth beetles, red flour beetles, and flat-headed red flour beetles
Negi et al. Persistent toxicity of certain newer insecticides on mulberry, rajmah bean and mung bean plants against Spodoptera litura (Fabricius)
Prasad et al. Extracts of the rosary pea, Abrus precatorius, are toxic to the invasive termite, Coptotermes gestroi
CN111387187A (en) Bemisia tabaci attractant composition and application thereof
Manzoor et al. Efficacy of Biflex and Fipronil in controlling subterranean termites (Isoptera: Rhinotermitidae) in different soils types in Pakistan
WO2017177294A1 (en) Natural insecticide
Doll et al. Changing insect pest management of pistachio and almond in California (2000 to 2014)

Legal Events

Date Code Title Description
A621 Written request for application examination

Free format text: JAPANESE INTERMEDIATE CODE: A621

Effective date: 20150126

A521 Request for written amendment filed

Free format text: JAPANESE INTERMEDIATE CODE: A821

Effective date: 20150126

A977 Report on retrieval

Free format text: JAPANESE INTERMEDIATE CODE: A971007

Effective date: 20150924

A131 Notification of reasons for refusal

Free format text: JAPANESE INTERMEDIATE CODE: A131

Effective date: 20151020

A521 Request for written amendment filed

Free format text: JAPANESE INTERMEDIATE CODE: A523

Effective date: 20151124

TRDD Decision of grant or rejection written
A01 Written decision to grant a patent or to grant a registration (utility model)

Free format text: JAPANESE INTERMEDIATE CODE: A01

Effective date: 20160119

A61 First payment of annual fees (during grant procedure)

Free format text: JAPANESE INTERMEDIATE CODE: A61

Effective date: 20160202

R150 Certificate of patent or registration of utility model

Ref document number: 5891546

Country of ref document: JP

Free format text: JAPANESE INTERMEDIATE CODE: R150

R250 Receipt of annual fees

Free format text: JAPANESE INTERMEDIATE CODE: R250

R250 Receipt of annual fees

Free format text: JAPANESE INTERMEDIATE CODE: R250

R250 Receipt of annual fees

Free format text: JAPANESE INTERMEDIATE CODE: R250

R250 Receipt of annual fees

Free format text: JAPANESE INTERMEDIATE CODE: R250

R250 Receipt of annual fees

Free format text: JAPANESE INTERMEDIATE CODE: R250

R250 Receipt of annual fees

Free format text: JAPANESE INTERMEDIATE CODE: R250