JP2012229196A - Attractant of nezara antennata - Google Patents
Attractant of nezara antennata Download PDFInfo
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- 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
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- 239000005667 attractant Substances 0.000 title claims abstract description 71
- 230000031902 chemoattractant activity Effects 0.000 title claims abstract description 62
- 241001521166 Nezara antennata Species 0.000 title abstract description 5
- MFZUVCQFJOAQLE-FZOXRXHISA-N (5S,6R)-2-methyl-5-[(2Z)-6-methylhepta-2,5-dien-2-yl]-7-oxabicyclo[4.1.0]hept-1-ene Chemical compound CC(C)=CC\C=C(\C)/[C@@H]1CCC(C)=C2[C@@H]1O2 MFZUVCQFJOAQLE-FZOXRXHISA-N 0.000 claims abstract description 20
- 241001581006 Dysaphis plantaginea Species 0.000 claims description 6
- YHBUQBJHSRGZNF-UHFFFAOYSA-N trans-α-Bisabolene Chemical compound CC(C)=CCC=C(C)C1CCC(C)=CC1 YHBUQBJHSRGZNF-UHFFFAOYSA-N 0.000 claims description 5
- YHBUQBJHSRGZNF-HNNXBMFYSA-N alpha-bisabolene Natural products CC(C)=CCC=C(C)[C@@H]1CCC(C)=CC1 YHBUQBJHSRGZNF-HNNXBMFYSA-N 0.000 claims description 2
- 230000000694 effects Effects 0.000 abstract description 14
- 229920001059 synthetic polymer Polymers 0.000 description 14
- 241000238631 Hexapoda Species 0.000 description 10
- 241000578422 Graphosoma lineatum Species 0.000 description 7
- 239000004698 Polyethylene Substances 0.000 description 6
- XTXRWKRVRITETP-UHFFFAOYSA-N Vinyl acetate Chemical compound CC(=O)OC=C XTXRWKRVRITETP-UHFFFAOYSA-N 0.000 description 6
- -1 polyethylene Polymers 0.000 description 6
- 229920000573 polyethylene Polymers 0.000 description 6
- 239000000126 substance Substances 0.000 description 6
- 241000894007 species Species 0.000 description 4
- 238000012360 testing method Methods 0.000 description 4
- 241000254173 Coleoptera Species 0.000 description 3
- YMWUJEATGCHHMB-UHFFFAOYSA-N Dichloromethane Chemical compound ClCCl YMWUJEATGCHHMB-UHFFFAOYSA-N 0.000 description 3
- 241000258937 Hemiptera Species 0.000 description 3
- 229920001577 copolymer Polymers 0.000 description 3
- 238000007334 copolymerization reaction Methods 0.000 description 3
- VLKZOEOYAKHREP-UHFFFAOYSA-N n-Hexane Chemical compound CCCCCC VLKZOEOYAKHREP-UHFFFAOYSA-N 0.000 description 3
- 238000002360 preparation method Methods 0.000 description 3
- YHBUQBJHSRGZNF-AUWJEWJLSA-N (Z)-alpha-bisabolene Chemical compound CC(C)=CC\C=C(\C)C1CCC(C)=CC1 YHBUQBJHSRGZNF-AUWJEWJLSA-N 0.000 description 2
- CSCPPACGZOOCGX-UHFFFAOYSA-N Acetone Chemical compound CC(C)=O CSCPPACGZOOCGX-UHFFFAOYSA-N 0.000 description 2
- RTZKZFJDLAIYFH-UHFFFAOYSA-N Diethyl ether Chemical compound CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 description 2
- OFBQJSOFQDEBGM-UHFFFAOYSA-N Pentane Chemical compound CCCCC OFBQJSOFQDEBGM-UHFFFAOYSA-N 0.000 description 2
- 241000607479 Yersinia pestis Species 0.000 description 2
- 239000004480 active ingredient Substances 0.000 description 2
- 235000013399 edible fruits Nutrition 0.000 description 2
- 238000000034 method Methods 0.000 description 2
- LQERIDTXQFOHKA-UHFFFAOYSA-N nonadecane Chemical compound CCCCCCCCCCCCCCCCCCC LQERIDTXQFOHKA-UHFFFAOYSA-N 0.000 description 2
- 239000003016 pheromone Substances 0.000 description 2
- FQTLCLSUCSAZDY-UHFFFAOYSA-N (+) E(S) nerolidol Natural products CC(C)=CCCC(C)=CCCC(C)(O)C=C FQTLCLSUCSAZDY-UHFFFAOYSA-N 0.000 description 1
- FQTLCLSUCSAZDY-SZGZABIGSA-N (E)-Nerolidol Natural products CC(C)=CCC\C(C)=C/CC[C@@](C)(O)C=C FQTLCLSUCSAZDY-SZGZABIGSA-N 0.000 description 1
- 229930014661 (Z)-alpha-bisabolene Natural products 0.000 description 1
- 229920000742 Cotton Polymers 0.000 description 1
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 1
- 244000068988 Glycine max Species 0.000 description 1
- 235000010469 Glycine max Nutrition 0.000 description 1
- FQTLCLSUCSAZDY-ATGUSINASA-N Nerolidol Chemical compound CC(C)=CCC\C(C)=C\CC[C@](C)(O)C=C FQTLCLSUCSAZDY-ATGUSINASA-N 0.000 description 1
- 241001671709 Nezara viridula Species 0.000 description 1
- 240000007594 Oryza sativa Species 0.000 description 1
- 235000007164 Oryza sativa Nutrition 0.000 description 1
- 241000209504 Poaceae Species 0.000 description 1
- 241000206607 Porphyra umbilicalis Species 0.000 description 1
- 239000000853 adhesive Substances 0.000 description 1
- 230000001070 adhesive effect Effects 0.000 description 1
- 150000001875 compounds Chemical class 0.000 description 1
- 238000007796 conventional method Methods 0.000 description 1
- 238000011161 development Methods 0.000 description 1
- 230000001747 exhibiting effect Effects 0.000 description 1
- 239000000835 fiber Substances 0.000 description 1
- 238000009472 formulation Methods 0.000 description 1
- 239000004615 ingredient Substances 0.000 description 1
- 235000021374 legumes Nutrition 0.000 description 1
- 239000000203 mixture Substances 0.000 description 1
- 239000004745 nonwoven fabric Substances 0.000 description 1
- 239000000123 paper Substances 0.000 description 1
- 239000002861 polymer material Substances 0.000 description 1
- 238000011160 research Methods 0.000 description 1
- 235000009566 rice Nutrition 0.000 description 1
- 239000002904 solvent Substances 0.000 description 1
- 230000008685 targeting Effects 0.000 description 1
- UFTFJSFQGQCHQW-UHFFFAOYSA-N triformin Chemical compound O=COCC(OC=O)COC=O UFTFJSFQGQCHQW-UHFFFAOYSA-N 0.000 description 1
- 235000013311 vegetables Nutrition 0.000 description 1
- 238000011179 visual inspection Methods 0.000 description 1
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- Agricultural Chemicals And Associated Chemicals (AREA)
Abstract
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.
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| 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 |
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| 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 |
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| JPN6015041076; Ｚｅｉｔｓｃｈｒｉｆｔ ｆｕｅｒ Ｎａｔｕｒｆｏｒｓｃｈｕｎｇ， Ｃ： Ｊｏｕｒｎａｌ ｏｆ Ｂｉｏｓｃｉｅｎｃｅｓ （１９９３） ４８ｃ, 1993, ７３-７９ * |
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