JPH0112722B2 - - Google Patents
Info
- Publication number
- JPH0112722B2 JPH0112722B2 JP29729585A JP29729585A JPH0112722B2 JP H0112722 B2 JPH0112722 B2 JP H0112722B2 JP 29729585 A JP29729585 A JP 29729585A JP 29729585 A JP29729585 A JP 29729585A JP H0112722 B2 JPH0112722 B2 JP H0112722B2
- Authority
- JP
- Japan
- Prior art keywords
- attractant
- acid
- valeric acid
- phenylethanol
- flies
- 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.)
- Expired
Links
- NQPDZGIKBAWPEJ-UHFFFAOYSA-N valeric acid Chemical compound CCCCC(O)=O NQPDZGIKBAWPEJ-UHFFFAOYSA-N 0.000 claims description 42
- WRMNZCZEMHIOCP-UHFFFAOYSA-N 2-phenylethanol Chemical compound OCCC1=CC=CC=C1 WRMNZCZEMHIOCP-UHFFFAOYSA-N 0.000 claims description 36
- 239000005667 attractant Substances 0.000 claims description 32
- 230000031902 chemoattractant activity Effects 0.000 claims description 31
- 241000607479 Yersinia pestis Species 0.000 claims description 24
- 239000002253 acid Substances 0.000 claims description 17
- 150000007513 acids Chemical class 0.000 claims description 12
- 239000000203 mixture Substances 0.000 claims description 7
- FERIUCNNQQJTOY-UHFFFAOYSA-N Butyric acid Chemical compound CCCC(O)=O FERIUCNNQQJTOY-UHFFFAOYSA-N 0.000 claims description 6
- XBDQKXXYIPTUBI-UHFFFAOYSA-N dimethylselenoniopropionate Natural products CCC(O)=O XBDQKXXYIPTUBI-UHFFFAOYSA-N 0.000 claims description 6
- KQNPFQTWMSNSAP-UHFFFAOYSA-N isobutyric acid Chemical compound CC(C)C(O)=O KQNPFQTWMSNSAP-UHFFFAOYSA-N 0.000 claims description 6
- FGKJLKRYENPLQH-UHFFFAOYSA-N isocaproic acid Chemical compound CC(C)CCC(O)=O FGKJLKRYENPLQH-UHFFFAOYSA-N 0.000 claims description 6
- XYHKNCXZYYTLRG-UHFFFAOYSA-N 1h-imidazole-2-carbaldehyde Chemical compound O=CC1=NC=CN1 XYHKNCXZYYTLRG-UHFFFAOYSA-N 0.000 claims description 3
- GWYFCOCPABKNJV-UHFFFAOYSA-M 3-Methylbutanoic acid Natural products CC(C)CC([O-])=O GWYFCOCPABKNJV-UHFFFAOYSA-M 0.000 claims description 3
- GWYFCOCPABKNJV-UHFFFAOYSA-N beta-methyl-butyric acid Natural products CC(C)CC(O)=O GWYFCOCPABKNJV-UHFFFAOYSA-N 0.000 claims description 3
- 235000019260 propionic acid Nutrition 0.000 claims description 3
- IUVKMZGDUIUOCP-BTNSXGMBSA-N quinbolone Chemical compound O([C@H]1CC[C@H]2[C@H]3[C@@H]([C@]4(C=CC(=O)C=C4CC3)C)CC[C@@]21C)C1=CCCC1 IUVKMZGDUIUOCP-BTNSXGMBSA-N 0.000 claims description 3
- 241000255925 Diptera Species 0.000 description 25
- 241000234282 Allium Species 0.000 description 20
- 235000002732 Allium cepa var. cepa Nutrition 0.000 description 18
- 241000084475 Delia antiqua Species 0.000 description 8
- 241000196324 Embryophyta Species 0.000 description 8
- 235000011389 fruit/vegetable juice Nutrition 0.000 description 6
- 235000006140 Raphanus sativus var sativus Nutrition 0.000 description 5
- 239000000877 Sex Attractant Substances 0.000 description 5
- 239000000126 substance Substances 0.000 description 5
- 238000012360 testing method Methods 0.000 description 5
- RTZKZFJDLAIYFH-UHFFFAOYSA-N Diethyl ether Chemical compound CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 description 4
- 235000005733 Raphanus sativus var niger Nutrition 0.000 description 4
- 240000001970 Raphanus sativus var. sativus Species 0.000 description 4
- 238000011161 development Methods 0.000 description 4
- 239000002410 kairomone Substances 0.000 description 4
- 241000238631 Hexapoda Species 0.000 description 3
- XEBKSQSGNGRGDW-UHFFFAOYSA-N kairomone Natural products CCCCCC=CCC(O)C(O)CCCCCCCC(O)=O XEBKSQSGNGRGDW-UHFFFAOYSA-N 0.000 description 3
- VLKZOEOYAKHREP-UHFFFAOYSA-N n-Hexane Chemical compound CCCCCC VLKZOEOYAKHREP-UHFFFAOYSA-N 0.000 description 3
- 241000894007 species Species 0.000 description 3
- 241001414896 Anthomyiidae Species 0.000 description 2
- 241000894006 Bacteria Species 0.000 description 2
- 241001609607 Delia platura Species 0.000 description 2
- 241001351188 Hylemya Species 0.000 description 2
- 241000190070 Sarracenia purpurea Species 0.000 description 2
- VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 description 2
- 230000002378 acidificating effect Effects 0.000 description 2
- 239000007864 aqueous solution Substances 0.000 description 2
- MNWFXJYAOYHMED-UHFFFAOYSA-N heptanoic acid Chemical compound CCCCCCC(O)=O MNWFXJYAOYHMED-UHFFFAOYSA-N 0.000 description 2
- FUZZWVXGSFPDMH-UHFFFAOYSA-N hexanoic acid Chemical compound CCCCCC(O)=O FUZZWVXGSFPDMH-UHFFFAOYSA-N 0.000 description 2
- 239000000843 powder Substances 0.000 description 2
- 239000002904 solvent Substances 0.000 description 2
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 2
- 241000251468 Actinopterygii Species 0.000 description 1
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 description 1
- 241000220259 Raphanus Species 0.000 description 1
- NIXOWILDQLNWCW-UHFFFAOYSA-N acrylic acid group Chemical group C(C=C)(=O)O NIXOWILDQLNWCW-UHFFFAOYSA-N 0.000 description 1
- 239000013543 active substance Substances 0.000 description 1
- 239000002775 capsule Substances 0.000 description 1
- 239000000969 carrier Substances 0.000 description 1
- 239000002975 chemoattractant Substances 0.000 description 1
- 238000007796 conventional method Methods 0.000 description 1
- 230000000694 effects Effects 0.000 description 1
- 235000013601 eggs Nutrition 0.000 description 1
- 238000011156 evaluation Methods 0.000 description 1
- 238000002474 experimental method Methods 0.000 description 1
- 235000019688 fish Nutrition 0.000 description 1
- 239000002917 insecticide Substances 0.000 description 1
- 239000007788 liquid Substances 0.000 description 1
- 238000004519 manufacturing process Methods 0.000 description 1
- 235000013379 molasses Nutrition 0.000 description 1
- 125000000896 monocarboxylic acid group Chemical group 0.000 description 1
- 230000007935 neutral effect Effects 0.000 description 1
- 230000029264 phototaxis Effects 0.000 description 1
- 230000003014 reinforcing effect Effects 0.000 description 1
- 238000011160 research Methods 0.000 description 1
- 239000005060 rubber Substances 0.000 description 1
- 239000004576 sand Substances 0.000 description 1
- 239000000741 silica gel Substances 0.000 description 1
- 229910002027 silica gel Inorganic materials 0.000 description 1
- 239000002689 soil Substances 0.000 description 1
- 238000001256 steam distillation Methods 0.000 description 1
- 230000002195 synergetic effect Effects 0.000 description 1
- 229920003002 synthetic resin Polymers 0.000 description 1
- 239000000057 synthetic resin Substances 0.000 description 1
Landscapes
- Agricultural Chemicals And Associated Chemicals (AREA)
Description
本発明は、Allium属植物(タマネギなど)の
害虫であるタマネギバエ、Hylemya antiqua
Meigen(Diptera:Anthomyiidae)、広範な植物
に加害するタネバエ、Hylemya platura
Meigen(Diptera:Anthomyiidae)などのヒレ
ミア属(Hylemya)害虫の誘引剤に関する。
タマネギバエ・Hylemya antiqua Meigenは
広く北半球に分布し、タマネギなどのAllium属
植物の重要害虫である。さらにまた、タネバエ・
H・Platura M.は加害作物が非常に広く、各種
農作物の発芽種子、幼植物を食害する世界的農業
害虫である。特にこれらの雌害虫は幼植物等の根
際近くに産卵し、このため幼虫が地下部を食害
し、作物を萎凋枯死いたらしめる。しかも、これ
らは土壌害虫であるため、殺虫剤による防除効果
が期待し難い。
さらに、ヒレミア属害虫として、前述の2種の
ほかにダイコン等を食害するダイコンバエ
(Hylemya floralis Fallen)、ヒメダイコンバエ
(H pilipyga VILLEN.)等が挙げられる。
従来、タマネギバエ、タネバエ等の誘引餌とし
て、それぞれタマネギ切片、タマネギ磨砕汁、糖
みつ、魚カス等が用いられている。しかし、これ
らの誘引餌は誘引力が不充分であるばかりでな
く、その製品により誘引力が一定していなかつた
り、あるいはその誘引力が時間と共に変化してし
まうため、化学誘引物質の利用が強く望まれてい
る。
近年、ガ類の害虫については、いわゆる性フエ
ロモンの構造が決定され、この誘引性の性フエロ
モンを用いて害虫の発生消長調査が行われるよう
になつている。しかし、ハエ類の性フエロモンは
その誘引力がガ類に比べて極めて弱く、たとえそ
の化学構造が決定されたとしても、発生消長調査
への利用は疑問視されている。また、一般に性フ
エロモンは雄害虫しか誘引しないので、加害の原
因となる雌害虫は減少せず、被害の直接的な軽減
はほとんど望むことができないのが現状である。
他方、害虫防除にカイロモン(Kairomone)
(異種個体間の情報伝達物質および生理活性物質
のうち受容側が利益を得るもの。例えば訪花性昆
虫では花の匂いなど)を利用する試みが始められ
ている。
タマネギバエ、タネバエに対する誘引力は、健
全植物よりも被害植物の方が強いことが以前より
知られているが、最近、これは植物体にバクテリ
アが作用して誘引カイロモンが作り出されるため
であることが明らかにされた。
本発明者は、バクテリアの作用により変性しつ
つあるタマネギバエ磨砕汁から誘引カイロモンの
分離同定を行い、この誘引カイロモンを用いるこ
とによりタマネギバエ、タネバエ等のヒレミア属
害虫の誘引剤を開発し、本発明を完成するに至つ
た。
本発明の目的は、タマネギバエ、タネバエ等の
ヒレミア属害虫の雌雄成虫あるいは幼虫を誘引、
捕獲してこれら害虫の発生密度を知り、これによ
り前記害虫の発生予察に役立ち得るのみならず、
大量誘殺によりこれら害虫による被害軽減、ある
いはこれら害虫の防除を達成し得、さらに誘引力
の変動が起こらないヒレミア属害虫の誘引剤を提
供することにある。
前述の目的を達成するため、本発明の誘引剤に
よれば、誘引性物質としてプロピオン酸、n−酪
酸、イソ−酪酸、n−吉草酸、イソ−吉草酸およ
びイソカプロン酸の酸類の群から選択された1種
またはそれ以上の混合物またはそれに2−フエニ
ルエタノールを組合せて含有することを特徴とす
る。
以下、本発明を具体的に詳述する。本発明に使
用する前述の誘引性物質は、次のようにして放置
タマネギ磨砕汁から抽出される。すなわち、強い
誘引力を有する放置タマネギ磨砕汁を減圧水蒸気
蒸留後、留出物をエーテルで抽出し、これを常法
により酸性および中性に分画し、中性画分から2
−フエニルエタノールを抽出し、かつ酸性画分か
らプロピオン酸、n−酪酸、イソ−酪酸、n−吉
草酸、イソ−吉草酸、およびイソカプロン酸の酸
類を抽出する。
これら酸類の誘引性物質は、いずれも強い誘引
力を有するものであるが、特にn−吉草酸の誘引
力は優れており、さらにこれらに2−フエニルエ
タノールが共存することにより一層優れた誘引力
を呈する。
本発明の誘引剤は、酸類の誘引性物質を単独ま
たは混合物として、あるいはそれに2−フエニル
エタノールを組合せて含有するものであるが、
水、ヘキサン、エーテル等の溶媒に溶解したもの
であつてもよい。好ましくは本発明の誘引剤は、
酸類に2−フエニルエタノールまたは、さらに好
ましくは、酸類としてn−吉草酸に2−フエニル
エタノールを併せて含有する。このような本発明
誘引剤は、プラスチツク製カプセルに封入した
り、あるいはゴム、合成樹脂、砂、シリカゲル、
セルロース粉末、その他の粉末、または粒状の担
体に吸着させて使用する。このような本発明誘引
剤を用いた誘引、捕獲の一例を示せば、溶剤、粉
剤、あるいはこれらを塗布あるいは含浸させた適
宜の成形物を、例えば水、その他の液体を入れた
バツト上あるいは適当な粘着物質を塗布した物体
上、またはその付近に設置することにより、タマ
ネギバエ、タネバエ等は本発明誘引剤によつて誘
引されてバツト中に落下され、または粘着物質に
捕獲されて死ぬ。
前述の本発明誘引剤によれば、タマネギバエ、
タネバエ等のヒレミア属害虫(雌雄成虫および幼
虫)を強力に誘引できるばかりでなく、誘引物質
の濃度、組成を所望の一定値に定めておけば、誘
引力の変動をきたすことがなく、このため標準誘
引製剤として使用することもでき、全国的な発生
の調査比較に利用できる。さらに本発明誘引剤に
よれば、性フエロモンとは違つて雌成虫も多数捕
獲することができるので、大量誘殺により被害の
直接的な軽減も可能であり、タマネギバエ、タネ
バエバエ等の重要害虫の防除へ寄与するところ多
大であり、さらに近縁種であるダイコンバエ、ヒ
メダイコンバエの防除も可能である。
以下、本発明を実施例により詳述する。
実施例 1
一般式CoH2o+1COOH(n=2〜6)の各酸類
(0.05%水溶液)について誘引力試験を行つた。
結果を表1に示した。
この誘引力試験は、次のとおりに行つた。先
ず、図に示すハエ捕獲器を用いて、札幌市豊平区
羊ケ丘1番地北海道農業試験場内の枠試験圃にお
いて前述の本発明誘引剤を第1図におけるシヤー
レ1に入れ、これに網状の蓋2を施す。この誘引
源をアクリル製透明トラツプ3の下に設置する
と、シヤーレ1内の本発明誘引剤は適度な速度で
大気中に拡散し、このためタマネギバエ、タネバ
エ等の雌雄はトラツプ3の下に誘引され、飛び立
つ際に走光性により孔4を通してトラツプ3内に
捕獲される。
表1において、数字は5トラツプ合計1日(午
後3時から翌朝午前9時)の捕獲数であり、また
nsは対照との間に有意差がないことを示す。
The present invention is directed to the onion fly, Hylemya antiqua, which is a pest of plants of the genus Allium (onions, etc.).
Meigen (Diptera: Anthomyiidae), a seed fly that injures a wide range of plants, Hylemya platura
Concerning an attractant for Hylemya pests such as Meigen (Diptera: Anthomyiidae). The onion fly Hylemya antiqua Meigen is widely distributed in the Northern Hemisphere and is an important pest of plants of the genus Allium such as onions. Furthermore, seed flies
H. Platura M. is a global agricultural pest that damages a wide range of crops and damages germinated seeds and young plants of various crops. In particular, these female pests lay eggs near the roots of young plants, etc., and their larvae feed on the underground parts, causing crops to wilt and die. Moreover, since these are soil pests, it is difficult to expect a control effect from insecticides. In addition to the above-mentioned two species, examples of pests of the genus Hylemia include Hylemya floralis Fallen and H pilipyga VILLEN., which damage radish and the like. Conventionally, onion slices, ground onion juice, molasses, fish scraps, etc. have been used as lures for onion flies, seed flies, etc., respectively. However, these lures not only have insufficient attracting power, but also the attracting power is not constant depending on the product, or the attracting power changes over time, so the use of chemical attractants is strongly required. desired. In recent years, the structure of so-called sex pheromone has been determined for moth pests, and this attractive sex pheromone has been used to investigate the development and development of pests. However, the attraction of the sex pheromone of flies is extremely weak compared to that of moths, and even if its chemical structure has been determined, its use in research on development and development is questionable. Furthermore, since sex pheromones generally attract only male pests, the number of female pests that cause damage cannot be reduced, and there is currently little hope of direct reduction of damage. On the other hand, Kairomone is used for pest control.
Attempts have begun to utilize substances that transmit information between individuals of different species and physiologically active substances that benefit the receiving side. For example, in flower-visiting insects, the scent of flowers, etc. It has long been known that damaged plants have a stronger attraction to onion flies and seed flies than healthy plants, but recently it has been shown that this is due to the production of attracting kairomones by bacteria acting on the plant body. revealed. The present inventor isolated and identified an attractant kairomone from the ground onion fly juice that is being denatured by the action of bacteria, and developed an attractant for onion fly, seed fly, and other pests of the genus Fillemia by using this attractant kairomone. I was able to complete it. The purpose of the present invention is to attract male and female adults or larvae of onion flies, seed flies, and other pests of the genus Fillemia.
By capturing these pests and knowing the density of their occurrence, this not only helps in predicting the occurrence of these pests, but also
It is an object of the present invention to provide an attractant for pests of the genus Hieremia, which can reduce damage caused by these pests or control them by mass-killing them, and which does not cause fluctuations in attracting power. To achieve the above object, according to the attractant of the present invention, the attractant is selected from the group of acids propionic acid, n-butyric acid, iso-butyric acid, n-valeric acid, iso-valeric acid and isocaproic acid. 2-phenylethanol. Hereinafter, the present invention will be specifically explained in detail. The above-mentioned attractant used in the present invention is extracted from the ground onion juice as follows. That is, after vacuum steam distillation of the left-ground onion juice, which has a strong attraction, the distillate is extracted with ether, and this is fractionated into acidic and neutral fractions by a conventional method.
- Extracting phenylethanol and extracting the acids propionic, n-butyric, iso-butyric, n-valeric, iso-valeric and isocaproic from the acidic fraction. All of these acid attractants have strong attraction, but the attraction of n-valeric acid is particularly excellent, and the coexistence of 2-phenylethanol with these makes it even more attractive. exhibit power. The attractant of the present invention contains an acid attractant alone or as a mixture, or in combination with 2-phenylethanol,
It may be dissolved in a solvent such as water, hexane, or ether. Preferably, the attractant of the present invention is
The acids include 2-phenylethanol, or more preferably, the acids include n-valeric acid and 2-phenylethanol. The attractant of the present invention may be encapsulated in a plastic capsule, or may be contained in rubber, synthetic resin, sand, silica gel,
It is used by adsorbing it on cellulose powder, other powders, or granular carriers. An example of attracting and capturing using the attractant of the present invention is to place a solvent, a powder, or an appropriate molded article coated or impregnated with these on a vat containing water or other liquid, or on an appropriate By placing the object on or near an object coated with a sticky substance, onion flies, seed flies, etc. are attracted by the attractant of the present invention and fall into the vat, or are captured by the sticky substance and die. According to the above-mentioned attractant of the present invention, onion fly,
Not only can it strongly attract pests of the genus Fillemia (male and female adults and larvae) such as seed flies, but if the concentration and composition of the attractant are set at a desired constant value, the attracting force will not fluctuate. It can also be used as a standard attractant and can be used to investigate and compare outbreaks across the country. Furthermore, unlike sex pheromones, the attractant of the present invention can also capture a large number of female adults, so it is possible to directly reduce damage by mass-killing, and is useful for controlling important pests such as onion fly and seed fly. This contributes greatly, and it is also possible to control the closely related species, the Japanese radish fly and the Japanese radish fly. Hereinafter, the present invention will be explained in detail with reference to Examples. Example 1 An attractive force test was conducted on each acid (0.05% aqueous solution) having the general formula C o H 2o+1 COOH (n=2 to 6).
The results are shown in Table 1. This attraction test was conducted as follows. First, using the fly trap shown in the figure, put the above-mentioned attractant of the present invention into the shear tray 1 shown in Fig. 1 in a frame test field in the Hokkaido Agricultural Experiment Station, No. 1 Hitsujigaoka, Toyohira-ku, Sapporo City, and place the net-like lid 2 on it. administer. When this attraction source is installed under the transparent acrylic trap 3, the attractant of the present invention in the shear tray 1 will diffuse into the atmosphere at a moderate rate, and therefore male and female onion flies, seed flies, etc. will be attracted to the bottom of the trap 3. When they take off, they pass through the hole 4 and are captured in the trap 3 by phototaxis. In Table 1, the numbers are the total number of catches in one day (from 3:00 pm to 9:00 am the next morning) from 5 traps, and
ns indicates no significant difference from control.
【表】
表1からわかるように試験した酸のうち、n−
カプロン酸、n−ヘプタン酸を除くすべての酸に
ついて誘引性が認められる。タマネギバエに対し
てはそれ程誘引力は強くないが、タネバエに対す
る誘引力は比較的強いことも表3からわかる。
実施例 2
表2の各種酸0.05%を含有する本発明誘引剤水
溶液に、2−フエニルエタノールをそれぞれ0.2
%添加し、該引数増加比率を測定した。表2の比
率Xは、
X=2−フエニルエタノール+酸の誘引数/2−フエニ
ルエタノール誘引数
の値であつて、5トラツプによる評価値である。[Table] As can be seen from Table 1, among the acids tested, n-
Attractivity is observed for all acids except caproic acid and n-heptanoic acid. Table 3 also shows that although the attraction to onion flies is not so strong, the attraction to seed flies is relatively strong. Example 2 0.2% of 2-phenylethanol was added to an aqueous solution of the attractant of the present invention containing 0.05% of the various acids listed in Table 2.
% was added, and the argument increase ratio was measured. The ratio X in Table 2 is the value of X=2-phenylethanol+acid attraction factor/2-phenylethanol attraction factor, and is an evaluation value based on 5 traps.
【表】
* 統計的に有意
表2からわかるように、酸に2−フエニールエ
タノールを添加することにより誘引力は有意に増
加する現象が認められた。特にn−吉草酸は共力
効果が高く、タマネギバエ、タネバエの捕獲数を
2.3倍〜4.3倍に増加させた。他の酸にも増加が認
められる場合もあるが。n−吉草酸が最も優れて
いると判断される。
実施例 3
2−フエニルエタノール0.2%の定量をn−吉
草酸の段階変化に添加する、すなわち、n−吉草
酸の最適濃度の探知について実施例1と同様に試
験を行い、結果を表3に示した。表1中、Pheは
2−フエニルエタノール、Valはn−吉草酸を示
し、数字は5トラツプ合計1日(午後3時から翌
朝午前9時)の捕獲数である。[Table] *Statistically significant As can be seen from Table 2, it was observed that the attraction force significantly increased by adding 2-phenylethanol to the acid. In particular, n-valeric acid has a high synergistic effect and reduces the number of onion flies and seed flies caught.
Increased from 2.3 times to 4.3 times. Although increases may also be observed in other acids. It is judged that n-valeric acid is the best. Example 3 A test was conducted in the same manner as in Example 1 to add a fixed amount of 0.2% of 2-phenylethanol to the step change of n-valeric acid, that is, to detect the optimal concentration of n-valeric acid, and the results are shown in Table 3. It was shown to. In Table 1, Phe represents 2-phenylethanol, Val represents n-valeric acid, and the numbers represent the total number of traps captured in one day (from 3:00 pm to 9:00 am the next morning).
【表】
表3からわかるように、段階変化するn−吉草
酸の濃度は総合的には0.05%が最も優れていると
判定される。しかし、タネバエに対しては1.25%
でもかなりの捕獲があり、一方、2−フエニルエ
タノールは0.2%の定量で、n−吉草酸の濃度が
変化するかなり広い範囲で助強効果があることを
示す。
実施例 4
n−吉草酸および2−フエニルエタノールの混
合剤、n−吉草酸の単独物質、および放置タマネ
ギ磨砕汁の誘引力比較試験を実施例1と同様に行
い、結果を表4に示した。表4中、Pheおよび
Valの各濃度は表3と同様であり、また放置タマ
ネギ磨砕汁は表2と同様であり、Iは4トラツプ
合計、1日の捕獲数を示す。[Table] As can be seen from Table 3, it is determined that 0.05% is the best overall concentration of n-valeric acid that changes in stages. However, 1.25% against seed flies
However, there was considerable capture, whereas 2-phenylethanol was determined at 0.2%, indicating that it has a reinforcing effect over a fairly wide range of varying concentrations of n-valeric acid. Example 4 An attractive force comparison test of a mixture of n-valeric acid and 2-phenylethanol, a single substance of n-valeric acid, and ground onion juice was conducted in the same manner as in Example 1, and the results are shown in Table 4. Indicated. In Table 4, Phe and
Each concentration of Val is the same as in Table 3, and the ground onion juice left standing is the same as in Table 2, and I indicates the total of 4 traps and the number of catches per day.
【表】
表4から自明なとおり0.05%n−吉草酸に0.2
%フエニルエタノールの混合剤は、n−吉草酸単
独で用いた場合よりも数倍誘引力が強く、また放
置タマネギ磨砕汁に対しても、タマネギバエでは
雌2.6〜5.0倍、雄1.8〜4.5、タネバエでは雌5.7倍
〜14.0倍、雄6.5倍〜7.4倍の誘引捕獲数を示し、
誘引力が非常に優れている。
表4中、第1のハエ捕獲状態は別紙参考写真
[1]のA、B、C、E各ゾーンにおいて示され
ている。
以上のとおり、本発明ではn−吉草酸単体とし
て、またさらに、n−吉草酸と2−フエニルエタ
ノールとの混合体として用いることによりタマネ
ギバエ、タネバエに対する一層強力な誘引力を示
すことがわかり、その他の酸でも同様に混合体に
すると相当な誘引力を示すことがわかる。本発明
は、例えば図に示す様に配置し、これをタマネギ
バ圃場に設置することによりその周囲に生息して
いる雌雄の成虫がトラツプへ誘引、捕獲されるの
で、タマネギバエ、タネバエ等の発生密度を知る
ことができるのみならず、大量の誘殺による害虫
防除、被害の軽減も可能となり、実用上極めて有
用な誘引剤である。
また、本発明は、ヒレミア属に属する重要害
虫、ダイコンバエ、ヒメダイコンバエに対しても
前述と同様に有効である。[Table] As is obvious from Table 4, 0.05% n-valeric acid contains 0.2
The mixture of % phenylethanol has several times stronger attraction than n-valeric acid alone, and also attracts onion flies 2.6 to 5.0 times more to females and 1.8 to 4.5 times more to males than n-valeric acid alone. , In the case of seed flies, females attracted 5.7 times to 14.0 times more, and males attracted 6.5 to 7.4 times more.
It has very good attracting power. In Table 4, the first fly capture state is shown in zones A, B, C, and E in the attached reference photo [1]. As described above, in the present invention, it has been found that using n-valeric acid alone or as a mixture of n-valeric acid and 2-phenylethanol exhibits a stronger attraction to onion flies and seed flies. It can be seen that other acids exhibit considerable attractive power when mixed in the same way. The present invention is arranged as shown in the figure, and by installing it in an onion fly field, adult male and female insects living around the trap are attracted to the trap and captured, thereby reducing the density of onion flies, seed flies, etc. It is a very useful attractant for practical purposes, as it not only allows you to know what is going on, but also allows you to control pests and reduce damage by attracting large amounts of insects. Furthermore, the present invention is also effective against important pests belonging to the genus Hieremia, such as the Japanese radish fly and the Japanese radish fly, in the same manner as described above.
(1) 図は本発明誘引剤を使用するためのハエ捕
獲器である。
1……シヤーレ、2……蓋、3……トラツ
プ、4……孔。
(2) 参考写真[I]はハエ捕獲状態を示すもので
ある。
(1) The figure shows a fly trap for using the attractant of the present invention. 1... Shear, 2... Lid, 3... Trap, 4... Hole. (2) Reference photo [I] shows the state of fly capture.
Claims (1)
酸、イソ−酪酸、n−吉草酸、イソ−吉草酸およ
びイソカプロン酸の酸類の群から選択された1種
またはそれ以上の混合物を含有することを特徴と
するヒレミア属害虫の誘引剤。 2 誘引性物質として、n−吉草酸を単独で含有
する特許請求の範囲第1項に記載の誘引剤。 3 誘引性物質として、プロピオン酸、n−酪
酸、イソ−酪酸、n−吉草酸、イソ−吉草酸およ
びイソカプロン酸の酸類の群から選択された1種
またはそれ以上の混合物に2−フエニルエタノー
ルを組合せて含有することを特徴とするヒレミア
属害虫の誘引剤。 4 誘引性物質として、n−吉草酸に2−フエニ
ルエタノールを組合せて含有する特許請求の範囲
第3項に記載の誘引剤。[Scope of Claims] 1. As an attractant, one or more mixtures selected from the group of acids propionic acid, n-butyric acid, iso-butyric acid, n-valeric acid, iso-valeric acid and isocaproic acid. An attractant for pests belonging to the genus Fillemia, characterized by containing the following. 2. The attractant according to claim 1, which contains n-valeric acid alone as the attractant. 3. As an attractant, 2-phenylethanol is added to a mixture of one or more acids selected from the group of acids propionic acid, n-butyric acid, iso-butyric acid, n-valeric acid, iso-valeric acid and isocaproic acid. An attractant for pests belonging to the genus Fillemia, characterized by containing a combination of the following. 4. The attractant according to claim 3, which contains a combination of n-valeric acid and 2-phenylethanol as the attractant.
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP29729585A JPS61165306A (en) | 1985-12-27 | 1985-12-27 | Attractant to inset pests in hylemya |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP29729585A JPS61165306A (en) | 1985-12-27 | 1985-12-27 | Attractant to inset pests in hylemya |
Related Parent Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
JP17363182A Division JPS5962504A (en) | 1982-10-01 | 1982-10-01 | Attractant for noxious insect belonging to genus hylemya |
Publications (2)
Publication Number | Publication Date |
---|---|
JPS61165306A JPS61165306A (en) | 1986-07-26 |
JPH0112722B2 true JPH0112722B2 (en) | 1989-03-02 |
Family
ID=17844658
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
JP29729585A Granted JPS61165306A (en) | 1985-12-27 | 1985-12-27 | Attractant to inset pests in hylemya |
Country Status (1)
Country | Link |
---|---|
JP (1) | JPS61165306A (en) |
-
1985
- 1985-12-27 JP JP29729585A patent/JPS61165306A/en active Granted
Also Published As
Publication number | Publication date |
---|---|
JPS61165306A (en) | 1986-07-26 |
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