JP2018029570A - Behavior inhibitor composition for terrestrial invertebrate - Google Patents

Behavior inhibitor composition for terrestrial invertebrate Download PDF

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JP2018029570A
JP2018029570A JP2016166363A JP2016166363A JP2018029570A JP 2018029570 A JP2018029570 A JP 2018029570A JP 2016166363 A JP2016166363 A JP 2016166363A JP 2016166363 A JP2016166363 A JP 2016166363A JP 2018029570 A JP2018029570 A JP 2018029570A
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behavior
active oil
terpineol
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計一 本田
Keiichi Honda
計一 本田
シズイ 本田
Shizui Honda
シズイ 本田
真友子 横田
Mayuko Yokota
真友子 横田
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Abstract

PROBLEM TO BE SOLVED: To solve problems in which most of conventional anesthetics for insects (organic chemicals) are harmful to a human body and are necessary to set appropriate conditions for each of insect species, also the carbon dioxide therapy being frequently used has drawbacks such as having a place of use limitation because an anesthesia time is short and special facilities and devices are required.SOLUTION: A behavior inhibitor is provided that is an external application agent simply available at every place to a wide range of terrestrial invertebrate species without using a special device and container, in which a highly safe specific natural plant essential oil component is assumed as active ingredients.SELECTED DRAWING: None

Description

本発明は、実験室内はもとより、野外においても簡便に陸生無脊椎動物の飛翔、歩行、逃避行動を人為的に抑制して、それらの捕獲やさまざまな処理を容易におこなえるようにするための、人体等に安全な行動抑制剤組成物に関するものである。   The present invention artificially suppresses flying, walking, and escape behavior of terrestrial invertebrates easily in the laboratory as well as outdoors, so that they can be easily captured and processed in various ways. The present invention relates to a behavior inhibitor composition safe for the human body and the like.

昆虫類を含めて、何らかの研究や実験のために室内で飼育したり、調査等の目的のために、野外で捕獲してマーキングなどをおこなう必要のある陸生無脊椎動物(以下、特に断らない限り、陸生無脊椎動物を単に「動物」と称する)の種類は多い。しかし、これらの動物の中にはガ、ハチ、トンボなどのように高度な飛翔能力を備えたものや、バッタ、クモ、ゴキブリなどのように素早く逃避するものも少なくない。   Terrestrial invertebrates (including insects) that need to be reared indoors for some research or experiment, or captured outdoors and marked for research purposes (unless otherwise noted) Terrestrial invertebrates are simply referred to as “animals”). However, many of these animals have advanced flight capabilities such as moths, bees, dragonflies, and others that escape quickly, such as grasshoppers, spiders, and cockroaches.

従って、このような動物を数えたり、移動させたり、固定して何らかの処理を施したりする場合には、予めこれらの動物を麻酔して殆ど動かないようにしておく必要があり、このための麻酔剤として、炭酸ガス、ジエチルエーテル、酢酸エチル、クロロホルムなどの薬剤が用いられたり、動物種によっては低温処理や水中麻酔法も利用される。 Therefore, when such animals are counted, moved, or fixed and subjected to any treatment, it is necessary to anesthetize these animals in advance so that they hardly move. As the agent, agents such as carbon dioxide, diethyl ether, ethyl acetate and chloroform are used, and depending on the animal species, low-temperature treatment and underwater anesthesia are also used.

しかし、動物種によって体サイズや体重が大きく異なるため、ジエチルエーテル、酢酸エチル、クロロホルムなどの薬品を使用する際には、吸入させる蒸気濃度の調節が難しく、不適切な麻酔処理によって動物が死亡することも少なくない。加えて、これらの薬品は人体に有害であるため、実験室内などの閉鎖空間での使用には細心の注意を要する。 However, body size and weight vary greatly depending on the animal species, so when using drugs such as diethyl ether, ethyl acetate, and chloroform, it is difficult to adjust the concentration of vapor to be inhaled, and animals die due to inappropriate anesthesia treatment There are many cases. In addition, since these chemicals are harmful to the human body, extreme care must be taken when using them in closed spaces such as laboratories.

一方、炭酸ガスによる麻酔は処理動物に対する生理的負担が少ないとされ、近年、汎用されるが、炭酸ガス雰囲気から動物を取り出すと数分程度で覚醒してしまうため、常に炭酸ガス雰囲気下で作業をせねばならず、通常、簡単な専用の装置を必要とする。従って、本法は野外で簡便に使用するのには適しておらず、上記の3種類の薬品も含めて、いずれも陸生無脊椎動物の麻酔には不完全な方法で、特に目的の動物を野外で捕獲・処理する場合には全く適していない。 On the other hand, anesthesia with carbon dioxide gas is said to have a low physiological burden on treated animals, and in recent years it is widely used. Usually requires a simple dedicated device. Therefore, this method is not suitable for convenient use in the field, and all of the above three drugs, including the above three drugs, are incomplete methods for anesthesia of terrestrial invertebrates. Not suitable for outdoor capture and processing.

さて、人体に対する全身麻酔においては、吸入麻酔法(亜酸化窒素ガス、セボフルラン、イソフルラン等の麻酔ガスを使用)や静脈麻酔法(プロポフォールやチオペンタール等の薬剤を使用)が、局所麻酔には表面麻酔や浸潤麻酔、伝達麻酔(リドカイン、ブピバカイン、ロピバカイン等を使用)などの方法がとられ、哺乳動物などの比較的大型の動物の捕獲に使用される麻酔銃には、ケタミン、エルトフィン、アセプロマジン等の麻酔剤や、場合によって鎮静剤、筋弛緩剤などが使用されるが、注射による麻酔は特に小型の無脊椎動物には適切でなく、しかもこれらの薬剤の多くは毒性が強く使用することはできない。   Now, in general anesthesia for the human body, inhalation anesthesia (using anesthesia gas such as nitrous oxide gas, sevoflurane, isoflurane) and intravenous anesthesia (using drugs such as propofol and thiopental), surface anesthesia for local anesthesia And invasive anesthesia, transmission anesthesia (using lidocaine, bupivacaine, ropivacaine, etc.), and anesthetic guns used to capture relatively large animals such as mammals include ketamine, ertophine, acepromazine, etc. Anesthetics and, in some cases, sedatives and muscle relaxants are used, but anesthesia by injection is not particularly appropriate for small invertebrates, and many of these drugs cannot be used because they are highly toxic. .

一方、天然植物精油の中には、蒸気吸入、経口摂取、体表面塗布などにより、人体や他の脊椎動物(魚類、ラットなど)に対して緩和な局所麻酔作用や鎮静作用を示すと言われるものが多数知られており、クロープ、シナモン、ハッカ、ペパーミント、イランイラン、イリス、スイートオレンジ、ローマンカモミール、カルダモン、クラリセージ、サイプレス、サンダルウッド、シトロネラ、ジンジャー、スペアミント、セダーウッド、ゼラニゥム、タンジェリン、ナツメグ、ネロリ、パイン、バジル、パチュリ、バニラ、バレリアン、ビターオレンジ、ベチバー、ベルガモット、安息香、マジョラム、マンダリン、レモンバーム、ヤロウ、ライム、ラベンダー、レモングラス、ローズ、ローズウッドなどの精油がそれらの例として挙げられる。   On the other hand, some natural plant essential oils are said to show mild local anesthetic and sedative effects on the human body and other vertebrates (fish, rats, etc.) by vapor inhalation, ingestion, and body surface application. Many things are known, such as cropes, cinnamon, peppermint, peppermint, ylang ylang, iris, sweet orange, roman chamomile, cardamom, clarisage, cypress, sandalwood, citronella, ginger, spearmint, cedarwood, geranium, tangerine, nutmeg, Examples include essential oils such as Neroli, Pine, Basil, Patchouli, Vanilla, Valerian, Bitter Orange, Vetiver, Bergamot, Benzo, Marjoram, Mandarin, Lemon Balm, Yarrow, Lime, Lavender, Lemongrass, Rose, Rosewood, etc. .

陸生無脊椎動物の行動(飛翔、歩行、跳躍)抑制には、適切な物質の蒸気吸入や、より望ましくは、体表面塗布(経皮吸収)よる方法が最も便利で実効性も期待されることから、上記の大部分の精油および、魚類もしくはラットに対する麻酔作用が報告されているクロープ油中の有効成分とされるオイゲノールやβ−カリオフィレン、人体への局所麻酔作用が知られているハッカ油やペパーミント油中の有効成分とされるl-メントール、鎮静作用が知られているセダーウッド油中のセドロール、レモンバーム油中のネリルアセテート、スイートオレンジ油中のリモネン、ラベンダー油、クラリセージ油やベルガモット油に含まれるリナリルアセテートやリナロール、さらに局所麻酔もしくは鎮静作用があると言われているビサボロール、カルバクロール、テルピネオール、シトロネラール、トシラール、カンファー、ボルネオール、フェンチョン、ジアセトンアルコールなどを用いて、予備的にハスモンヨトウの終齢幼虫およびクサギカメムシ成虫に対する行動抑制効果を、一定条件の下で、蒸気吸入法と体表面塗布法により評価した。 For the suppression of terrestrial invertebrate behavior (flying, walking, jumping), vapor inhalation of an appropriate substance and, more desirably, a method using body surface application (transdermal absorption) is expected to be the most convenient and effective. Eugenol and β-caryophyllene, which are active ingredients in the above-mentioned essential oils, and crope oil, which has been reported to have anesthetic action on fish or rats, mint oil, which is known to have local anesthetic action on the human body, Contains l-menthol, an active ingredient in peppermint oil, cedrol in cedarwood oil, which is known to be sedative, neryl acetate in lemon balm oil, limonene in sweet orange oil, lavender oil, clarisage oil and bergamot oil Linalyl acetate and linalool, bisabolol and carbacarb, which are said to have local anesthetics or sedation Using a crawl, terpineol, citronellal, tosilal, camphor, borneol, fenchon, diacetone alcohol, etc. And body surface coating method.

しかし、蒸気吸入法では30分以上経過しても殆どの精油や精油成分に目立った行動抑制効果がみられず、一方、体表面塗布法では一部の精油に軽度の抑制効果が観察されたものの充分ではなく、その他の精油では全く効果がないか、逆に中毒症状を示して死亡する場合もみられた。また、個別の精油成分の試験でも満足な抑制効果はみられず、ごく一部の成分では急性毒性によるものか、死亡する場合が観察された。このように、脊椎動物と無脊椎動物とでは化合物の作用機序や生理作用が異なるためか、脊椎動物で報告されている知見をそのまま無脊椎動物に当てはめることができない。従って多種類の化合物と動物種を対象とした独自の詳細な試験結果に基づいて、人体に安全で新規な陸生無脊椎動物用行動抑制剤の開発が望まれていた。 However, in the steam inhalation method, no significant action suppression effect was observed in most essential oils and essential oil components even after 30 minutes or more, while in the body surface application method, a slight suppression effect was observed in some essential oils. However, it was not sufficient, and other essential oils were not effective at all, or conversely, poisoning was observed and death occurred. In addition, tests with individual essential oil components did not show a satisfactory inhibitory effect, and only a few components were observed to be due to acute toxicity or death. Thus, the vertebrates and invertebrates cannot apply the findings reported in vertebrates as they are because the action mechanism and physiological action of the compounds are different. Therefore, it has been desired to develop a novel action inhibitor for terrestrial invertebrates that is safe for the human body based on unique detailed test results for various kinds of compounds and animal species.

Anaesthesia, 53: 720-721, 1996.Anaesthesia, 53: 720-721, 1996. Farmaco, 56: 387-389, 2001.Farmaco, 56: 387-389, 2001. Brazilian Journal of Medical and Biological Research, 34:1337-1340, 2001.Brazilian Journal of Medical and Biological Research, 34: 1337-1340, 2001. The International Journal of Aromatherapy, 15: 7-14, 2005.The International Journal of Aromatherapy, 15: 7-14, 2005. Planta Medica, 76: 1647-1653, 2010.Planta Medica, 76: 1647-1653, 2010. African Journal of Biotechnology, 9: 6566-6572, 2010.African Journal of Biotechnology, 9: 6566-6572, 2010. Comparative Biochemistry and Physiology, Part C, 155: 462-468, 2012.Comparative Biochemistry and Physiology, Part C, 155: 462-468, 2012. Fish Physiology and Biochemistry, 40: 701-714, 2014.Fish Physiology and Biochemistry, 40: 701-714, 2014. Journal of Limnology and Freshwater Fisheries Research, vol.1, 2015.Journal of Limnology and Freshwater Fisheries Research, vol.1, 2015. Journal of Traditional and Complementary Medicine, 6: 140-145, 2016.Journal of Traditional and Complementary Medicine, 6: 140-145, 2016.

解決しようとする問題点としては、既存の昆虫などに使う麻酔剤の中で有機性薬品を使う場合は、昆虫種ごとに適切な蒸気濃度と暴露時間を設定する必要が有るが、これは処理温度(周囲の気温)の影響を受けると共に、対象昆虫種の発育段階(ステージ)によっても大きく変わるため、適切な麻酔条件を見出すのに熟練を要したり、煩雑な予備実験を必要とすること、またそれによって多くの個体を死亡させてしまう恐れが大きいこと、加えて作業中の蒸気吸入による人体(試験担当者)への悪影響が強く懸念されること、また一方、炭酸ガス麻酔においては、麻酔からの回復が比較的早いために、常に炭酸ガス雰囲気下で作業する必要が有り、そのために特別な装置を必要とすること、従って野外での作業には不向きで、捕獲調査等には使用できないこと、などが挙げられる。 The problem to be solved is that when using organic chemicals among the anesthetics used for existing insects, it is necessary to set an appropriate vapor concentration and exposure time for each insect species. As it is affected by the temperature (ambient temperature) and changes greatly depending on the stage of development of the target insect species, it requires skill to find appropriate anesthesia conditions or requires complicated preliminary experiments. In addition, there is a great risk that many individuals will be killed by it, and in addition, there is a strong concern about the adverse effects on human bodies (testers) due to vapor inhalation during work, while in carbon dioxide anesthesia, Because recovery from anesthesia is relatively fast, it is necessary to always work in a carbon dioxide atmosphere, and therefore special equipment is required, so it is not suitable for outdoor work and is not suitable for capture investigations. That you can not use, and the like.

本発明は、安全性の高い特定の天然植物精油成分を活性成分とする組成物からなり、特別な装置や容器を用いることなく、あらゆる場所で使用可能な外用塗布剤であり、動物の飛翔、歩行、跳躍などの運動機能を生理的に阻害することにより、諸行動を抑制することを主要な特徴とする。   The present invention comprises a composition comprising a highly safe specific natural plant essential oil component as an active ingredient, and is an external application agent that can be used everywhere without using a special device or container. The main feature is to suppress various actions by physiologically inhibiting motor functions such as walking and jumping.

具体的には、活性成分として、(1)シトラール(シトラール−aまたはシトラール−b、及びそれらの任意割合の混合物を含む)、(2)テルピネオール(α−テルピネオール、β−テルピネオール、γ−テルピネオール、δ−テルピネオールのいずれか一つ、またはそれらの任意割合の混合物を含む)、(3)酢酸テルピニル(α−テルピニルアセテート、β−テルピニルアセテート、γ−テルピニルアセテート、δ−テルピニルアセテートのいずれか一つ、またはそれらの任意割合の混合物を含む)で示される(1)〜(3)の3群の中から選択した少なくとも1つの群で構成される精油に、必要に応じて適量の界面活性剤を添加して、さらに必要に応じて希釈剤としての鉱油や油脂に溶解する方法、あるいは、(1)〜(3)の中から選択した少なくとも1つの群で構成される精油、またはそれを鉱油や油脂に溶解した油性液を、界面活性剤を用いて水中で乳化分散する方法などにより、本発明を完成した。 Specifically, as an active ingredient, (1) citral (including citral-a or citral-b and a mixture thereof in any proportion), (2) terpineol (α-terpineol, β-terpineol, γ-terpineol, any one of δ-terpineol, or a mixture thereof in any proportion), (3) terpinyl acetate (α-terpinyl acetate, β-terpinyl acetate, γ-terpinyl acetate, δ-terpine) An essential oil composed of at least one group selected from the three groups of (1) to (3) represented by any one of pinyl acetate or a mixture thereof in any proportion) A method of adding an appropriate amount of a surfactant according to necessity and further dissolving in mineral oil or fat as a diluent, if necessary, or (1) to (3) Thus, the present invention has been completed by a method of emulsifying and dispersing an essential oil composed of at least one group or an oily liquid obtained by dissolving it in mineral oil or fat in water using a surfactant.

ここで使用する希釈剤としての鉱油は、ケロシン、軽油、マシン油、流動パラフィンなどの炭化水素類(これらのいずれか一つ、または任意割合の混合物を含む)で、油脂類としては、ナタネ油、コーン油、ダイズ油、アマニ油、オリーブ油、ゴマ油、ツバキ油、ヒマシ油、落花生油、ヤシ油、パーム油、キリ油、サフラワー油、ヒマワリ油、マツ実油、アサ実油、綿実油、ヌカ油、グレープフルーツ種油、ヘントウ油、イワシ油、ニシン油、鯨油、牛脂、豚脂などやそれらの混合油脂が挙げられるが、これらに限定されるものではない。   Mineral oil as a diluent used here is a hydrocarbon such as kerosene, light oil, machine oil, liquid paraffin (including any one of these or a mixture of any ratio), and as fats and oils, rapeseed oil is used. , Corn oil, soybean oil, linseed oil, olive oil, sesame oil, camellia oil, castor oil, peanut oil, coconut oil, palm oil, kiri oil, safflower oil, sunflower oil, pine seed oil, Asa seed oil, cottonseed oil, nutca Examples thereof include, but are not limited to, oil, grapefruit seed oil, gentian oil, sardine oil, herring oil, whale oil, beef tallow, lard, and the like.

ここで使用する界面活性剤としては、一般に乳化剤、分散剤、可溶化剤として利用される種々の非イオン系界面活性剤(例えばソルビタン脂肪酸エステル、ポリオキシエチレンソルビタン脂肪酸エステル、ショ糖脂肪酸エステル、グリセリン脂肪酸エステル、ポリエチレングリコール脂肪酸エステル、脂肪酸ジエタノールアミド、ポリオキシエチレンアルキルフェニルエーテル、ポリグリセリン脂肪酸エステル、プロピレングリコール脂肪酸エステル、ポリオキシエチレンアルキルエーテルなどが挙げられるが、これらに限定されるものではない)および陰イオン系界面活性剤(アルキル硫酸エステル塩、ポリオキシエチレンアルキルエーテル硫酸エステル塩、アルキルスルホン酸塩、アルキルベンゼンスルホン酸塩、脂肪酸塩、アルキルリン酸エステル塩などが挙げられるが、これらに限定されるものではない)を用いることが可能であるが、動物に対する負荷の観点からは、ソルビタン脂肪酸エステルやショ糖脂肪酸エステルなどがより好ましい。   As the surfactant used here, various nonionic surfactants generally used as emulsifiers, dispersants, solubilizers (for example, sorbitan fatty acid ester, polyoxyethylene sorbitan fatty acid ester, sucrose fatty acid ester, glycerin) Fatty acid esters, polyethylene glycol fatty acid esters, fatty acid diethanolamides, polyoxyethylene alkyl phenyl ethers, polyglycerin fatty acid esters, propylene glycol fatty acid esters, polyoxyethylene alkyl ethers, etc., but are not limited thereto) and Anionic surfactant (alkyl sulfate ester salt, polyoxyethylene alkyl ether sulfate ester salt, alkyl sulfonate salt, alkyl benzene sulfonate salt, fatty acid salt, alkyl salt Although such ester salts, it is possible to use a not be) to be limited to these, from the viewpoint of load to the animal, such as sorbitan fatty acid esters and sucrose fatty acid esters are more preferable.

このようにして得られた組成物を、対象とする陸生無脊椎動物(昆虫類、クモ・ダニ類、ムカデ・ヤスデ類、ダンゴムシ類などの節足動物、ミミズ・ヒル類などの環形動物、カタツムリ・ナメクジ類などの軟体動物)に適量を直接散布することにより所期の目的を達成することができる。   The composition thus obtained was applied to target terrestrial invertebrates (arthropods such as insects, spiders and ticks, centipedes and millipedes, dandelions, annelids such as earthworms, snails, etc.)・ The desired purpose can be achieved by spraying a suitable amount directly onto mollusks such as slugs.

本発明の組成物は、麻酔作用や鎮静作用により動物の行動を抑制すると考えられるが、作用が比較的緩和なため塗布量の範囲(幅)が広く、適用可能な対象動物の種類が多いという大きな特徴を有するとともに、塗布過多による生理異常や死亡を回避できる一方、逆に塗布量が不足していると判断される場合には、対象動物(個体)の様子を見ながら適宜、反復塗布も可能で、確実に行動抑制を達成できるという長所も有する。   The composition of the present invention is considered to suppress the behavior of animals by anesthesia and sedation, but because the action is relatively relaxed, the application amount range (width) is wide, and there are many types of target animals that can be applied. While it has major features and can avoid physiological abnormalities and death due to excessive application, on the other hand, if it is determined that the application amount is insufficient, repeated application can be performed appropriately while observing the state of the target animal (individual). It also has the advantage of being able to achieve action suppression with certainty.

本発明の組成物は、活性成分の塗布濃度の調節も容易なため、同一動物種に対しても発育段階に応じた適切な濃度処理が可能である。従って、使用に際して特別な技術や経験を要せず、必要に応じて塗布量・回数の調節をおこなうことにより、簡便に対象動物の行動を適切に抑制することができる。さらに行動抑制時間を延長したい場合にも、対象動物の様子を考慮しつつ、追加塗布により実現が可能となる。 Since the composition of the present invention can easily adjust the application concentration of the active ingredient, it is possible to appropriately treat the same animal species according to the developmental stage. Therefore, the behavior of the target animal can be easily and appropriately suppressed by adjusting the application amount and the number of times as needed without requiring special techniques or experience in use. Furthermore, even when it is desired to extend the behavior suppression time, it can be realized by additional application while taking into consideration the state of the target animal.

本発明の組成物の動物への塗布は、ハンドスプレーもしくは噴射剤を加えたスプレーを使用することにより極めて簡便におこなうことができるので、特別な設備や装置、容器などを全く必要としない。それゆえ、実験室内は勿論のこと、フィールドなどにおける動物の捕獲・調査などにも利用できるという、これまでない大きな利点も有する。   Application of the composition of the present invention to an animal can be carried out very easily by using a hand spray or a spray containing a propellant, so that no special equipment, apparatus, container, or the like is required. Therefore, it has an unprecedented great advantage that it can be used not only in the laboratory but also for capturing and investigating animals in the field.

本発明の組成物を構成する基本配合原材料には、食品添加物として許可された香料や鉱油、油脂が少なくないため、原材料を適切に選択することにより、人畜に対する安全性の高い商品の提供が可能である。また、香料成分は全て天然の植物由来素材であって、野外で使用しても微生物、空気、紫外線等により比較的短期間で資化・分解されるために土壌残留性が無く、従って環境汚染度が極めて低いという特徴も備えている。   Since the basic blending raw materials constituting the composition of the present invention are not limited to fragrances, mineral oils, and fats and oils that are permitted as food additives, it is possible to provide products that are highly safe for human livestock by appropriately selecting the raw materials. Is possible. In addition, the fragrance ingredients are all natural plant-derived materials, and even when used outdoors, they are assimilated and decomposed by microorganisms, air, ultraviolet rays, etc. in a relatively short period of time, so there is no soil persistence, thus environmental pollution. It also has the feature that the degree is extremely low.

本発明の組成物は、植物精油中に存在する特定種類の活性成分に、必要に応じて適量の界面活性剤を加え、さらに必要に応じて鉱油や油脂で混和・希釈した油性混合液、あるいは、活性成分をそのまま、またはその油性混合液を常法により界面活性剤を用いて水中で乳化分散して水性乳化液を製造することによって得られ、これらの油性混合液や水性乳化液を噴霧器を用いて、あるいはこれにLPGやジメチルエーテルなどの噴射剤を加えて、動物に塗布することにより本発明の目的を達成することができる。   The composition of the present invention is an oily mixture obtained by adding an appropriate amount of a surfactant as necessary to a specific type of active ingredient present in a plant essential oil, and further mixing and diluting with mineral oil or fat as necessary, or The active ingredient is obtained as it is, or the oily mixture is emulsified and dispersed in water by using a surfactant in a conventional manner to produce an aqueous emulsion. The object of the present invention can be achieved by using or applying a propellant such as LPG or dimethyl ether to animals.

以下に、界面活性剤として、特にショ糖脂肪酸エステルやソルビタン脂肪酸エステルを用いた例を実施例によって具体的に説明するが、これらは例示に過ぎず、本発明の組成物を制限するものではない。 In the following, examples using sucrose fatty acid esters and sorbitan fatty acid esters as surfactants will be specifically described by way of examples, but these are merely examples and do not limit the composition of the present invention. .

シトラール、テルピネオール、酢酸テルピニルを表1に示した重量比で組み合わせた5種類の活性成分液(以下、活性油と称す)A,B,C,D,Eを調製した(表1)。
Five active ingredient liquids (hereinafter referred to as “active oils”) A, B, C, D, and E, in which citral, terpineol, and terpinyl acetate were combined in the weight ratio shown in Table 1 were prepared (Table 1).

表2に示した処方で、活性油A〜Eのそれぞれに対して、各水性乳化液試料を製造するためのベース液を調製した。乳化液試料は、処方に記した活性油の所定量を通常の方法で乳化することにより容易に得られる。
The base liquid for manufacturing each aqueous | water-based emulsion liquid sample was prepared with respect to each of active oil AE by the prescription shown in Table 2. The emulsified liquid sample can be easily obtained by emulsifying a predetermined amount of the active oil described in the formulation by a usual method.

表3に示した処方で、活性油A〜Eのそれぞれに対して、各油性液を製造するためのベース液を設定した。油性液試料は、処方に記した活性油を用いて、その所定量を必要に応じて所定量のソルビタン脂肪酸エステルと常温で混合・溶解し、さらに所定量の鉱油や油脂(それらの混合物も含む)で希釈することにより容易に得られる。
In the formulation shown in Table 3, a base solution for producing each oily solution was set for each of the active oils A to E. The oily liquid sample is prepared by mixing and dissolving a predetermined amount with a predetermined amount of sorbitan fatty acid ester at room temperature as necessary using the active oil described in the formulation, and further including a predetermined amount of mineral oil or fat (and mixtures thereof) ) To obtain easily.

活性油各2gを用いて、表2に示した処方で水性乳化液試料を20種類調製した。(方法)室温で、所定の活性油に所定のショ糖脂肪酸エステルの水溶液をよく撹拌しながら加え、全量を100gとした。その後、これを400rpmで2分間混合撹拌して乳化液試料AM(2)〜EO(2)(括弧内の数値は活性油の配合%を示す。以下同様)を得た。調製した乳化液試料の均質性(外観)にはそれぞれ若干の違いは見られたものの、いずれも白色〜淡黄白色の概ね良好な乳化液が得られた。 Twenty kinds of aqueous emulsion samples were prepared using 2 g of each of the active oils with the formulation shown in Table 2. (Method) An aqueous solution of a predetermined sucrose fatty acid ester was added to a predetermined active oil with stirring well at room temperature to make a total amount of 100 g. Thereafter, this was mixed and stirred at 400 rpm for 2 minutes to obtain emulsion samples AM (2) to EO (2) (the values in parentheses indicate the blending percentage of the active oil, the same applies hereinafter). Although a slight difference was observed in the homogeneity (appearance) of the prepared emulsion samples, a generally good emulsion of white to pale yellowish white color was obtained.

活性油各5gを用いて、表3に示した処方で油性液試料を19種類調製した。(方法)所定の活性油に所定量のソルビタン脂肪酸エステルを加えて70℃で充分に混和した後、そこに70℃に加温したケロシンを加えて全量を100gとし、油性液試料SAOs(5)〜SEO(5)を得た。いずれも殆ど透明〜ごく僅かに濁った無色〜微黄色のやや粘性のある液であった。 19 kinds of oily liquid samples were prepared with the formulation shown in Table 3 using 5 g of each active oil. (Method) After adding a predetermined amount of sorbitan fatty acid ester to a predetermined active oil and mixing well at 70 ° C., kerosene heated to 70 ° C. is added to make the total amount 100 g, and oily liquid sample SAOs (5) ~ SEO (5) was obtained. All were almost transparent, very slightly turbid, colorless to slightly yellow, slightly viscous liquid.

実施例5において、活性油各20gを用い、ケロシンの代わりにヒマシ油を用いる以外は全く同様の処方・方法により油性液試料を19種類調製した。次にこれらの油性液を用い、実施例4おいて、表2記載の活性油をこれらの油性液に置きかえる以外は全く同様の方法により、表2、表3において同じ番号に対応する処方で水性乳化液試料を19種類調製した。いずれも実施例4で得られた乳化液と同様、白色〜微黄白色の概ね良好な乳化液が得られ、活性油を希釈した油性液からも容易に水性乳化液試料の調製が可能である。 In Example 5, 19 types of oily liquid samples were prepared by exactly the same formulation and method except that 20 g of each active oil was used and castor oil was used instead of kerosene. Next, using these oily liquids, in Example 4, except that the active oils listed in Table 2 were replaced with these oily liquids, the same formulas corresponding to the same numbers in Tables 2 and 3 were used. Nineteen emulsion samples were prepared. In any case, as with the emulsion obtained in Example 4, a white to slightly yellowish white emulsion is obtained, and an aqueous emulsion sample can be easily prepared from an oily liquid obtained by diluting active oil. .

表2記載の2,5,12,15及び18番のベース液を用い、実施例4と同様の方法で、それぞれの活性油について配合量(%)が0.01,0.03,0.05,0.1,0.3の水性乳化液試料を調製した。ハンドスプレーを用い、25℃に設定した室内で、それらの乳化液をアオムシコバチ成虫に対して約15cmの距離から各1回ずつ塗布して、その後の行動を観察した。各試験試料ごとに20匹の個体を使用し、正常な飛翔ができない場合を行動抑制効果あり、と判定した。3分以内に行動抑制が見られた個体の数と、それら個体の行動抑制時間(分)の平均値(括弧内に記載)を表4に示した。
Using the base solutions Nos. 2, 5, 12, 15 and 18 listed in Table 2, the amount (%) of each active oil was 0.01, 0.03, 0.0 in the same manner as in Example 4. An aqueous emulsion sample of 05, 0.1, 0.3 was prepared. Using a hand spray, in a room set at 25 ° C., these emulsions were applied once to each adult beetle from a distance of about 15 cm, and the subsequent behavior was observed. Twenty individuals were used for each test sample, and a case where normal flight was not possible was determined to have a behavior suppressing effect. Table 4 shows the number of individuals whose behavior was suppressed within 3 minutes and the average value (described in parentheses) of the behavior suppression time (minutes) of these individuals.

表4から明らかなように、いずれのベース液においても活性油の濃度が0.05%未満では行動抑制効果は極めて不充分であり、アオムシコバチのような小型昆虫についても、少なくとも0.05%以上は必要であることが分かる。   As is clear from Table 4, in any base solution, when the concentration of the active oil is less than 0.05%, the action-suppressing effect is extremely insufficient, and even for small insects such as the bee, at least 0.05% It turns out that the above is necessary.

表2記載の3,8,10,13及び17番のベース液を用い、実施例7と同様にして活性油の配合量の異なる水性乳化液試料を調製した。各試験試料ごとに20匹のヒトスジシマカを用いて、実施例7と同様の条件・方法で塗布・試験をおこない、行動抑制効果を評価した。結果を表5に示したが、実施例7と同様、活性油の濃度が0.05%未満では行動抑制効果は極めて不充分であり、カのような小型昆虫についても、少なくとも0.05%以上は必要であることが分かる。
Using the base solutions of Nos. 3, 8, 10, 13, and 17 shown in Table 2, aqueous emulsion samples having different active oil blending amounts were prepared in the same manner as in Example 7. Using 20 human striped mosquitoes for each test sample, application / test was performed under the same conditions and methods as in Example 7 to evaluate the action inhibitory effect. The results are shown in Table 5. As in Example 7, when the concentration of the active oil is less than 0.05%, the action-suppressing effect is extremely insufficient, and even for small insects such as mosquitoes, at least 0.05% It turns out that the above is necessary.

表3記載の1,5,8,13,15及び19番の油性ベース液を用い、実施例5と同様の方法で、それぞれの活性油について配合量(%)が0.01,0.03,0.05,0.1,0.3の油性液試料を各100g調製した。次いで、それぞれを300gのLPGと共に耐圧容器に封入して、油性スプレー試料を作製した。25℃に設定した室内で、試験試料ごとに20匹のオンシツコナジラミを用いて、約30cmの距離から2秒間スプレーを噴射して行動抑制効果を評価した。結果を表6に示したが、実施例7,8と同様、活性油の濃度が0.05%未満では行動抑制効果は不充分であった。
Using the oily base solutions of Nos. 1, 5, 8, 13, 15 and 19 listed in Table 3, the amount (%) of each active oil was 0.01, 0.03 in the same manner as in Example 5. , 0.05, 0.1 and 0.3 oily liquid samples were prepared for each 100 g. Next, each was sealed in a pressure-resistant container together with 300 g of LPG to prepare an oil-based spray sample. In a room set at 25 ° C., 20 on-site white lice were used for each test sample, and a spray was sprayed for 2 seconds from a distance of about 30 cm to evaluate the action suppressing effect. The results are shown in Table 6. As in Examples 7 and 8, when the concentration of the active oil was less than 0.05%, the action suppressing effect was insufficient.

これらのことから、水性乳化液、油性液のいずれにおいても、どの活性油でも少なくとも0.05%以上を使用しないと、小型の昆虫類についても充分な行動抑制効果を発揮し得ないことが分かる。 From these facts, it is understood that, in any of the aqueous emulsion and oily liquid, if any active oil is not used at least 0.05% or more, it cannot exert a sufficient action suppressing effect even for small insects. .

表2記載の乳化液用ベース液1番(AM)を用いて、実施例4と同様の方法で活性油(A)の配合量(%)が0.3,0.5,1,3,5,10の水性乳化液試料を調製した。ハンドスプレーを用い、25℃に設定した室内で、それらの乳化液を以下の10種類の無脊椎動物に対して約15cmの距離から各1回ずつ塗布して、その後の行動を観察した。各動物種はそれぞれ20匹の個体を使用し、正常な飛翔ができない場合、または自身の体長の約5倍以上の距離を移動できない場合を行動抑制効果あり、と判定した。3分以内に行動抑制が見られた個体の数と、それら個体の行動抑制時間(分)の平均値(括弧内に記載)を表7に示した。尚、試料によっては死亡個体が生じたが、その場合にはカギ括弧内に死亡した個体数を示した。1:フタモンアシナガバチ,2:ナミハダニ,3:キイロスズメバチ,4:チャコウラナメクジ,5:ヤマビル,6:ショウジョウバエ,7:オオタバコガ(成虫),8:ニセダイコンアブラムシ,9:ハリブトシリアゲアリ,10:チュウレンジバチ(幼虫)
Using the base solution No. 1 (AM) for the emulsified liquid described in Table 2, the compounding amount (%) of the active oil (A) is 0.3, 0.5, 1, 3, and 3 in the same manner as in Example 4. 5,10 aqueous emulsion samples were prepared. Using a hand spray, in a room set at 25 ° C., these emulsions were applied once to each of the following 10 invertebrates from a distance of about 15 cm, and the subsequent behavior was observed. Each animal species used 20 individuals, and when it was not possible to fly normally, or when it was not able to move a distance of about 5 times or more of its own body length, it was determined that there was an action suppressing effect. Table 7 shows the number of individuals in which behavioral inhibition was observed within 3 minutes and the average value (described in parentheses) of behavioral inhibition time (minutes) of these individuals. Depending on the sample, dead individuals were generated. In that case, the number of dead individuals is shown in the brackets. 1: phthalmon wasp, 2: nymph mite, 3: killer whale, 4: chakoura slug, 5: yamabir, 6: drosophila, 7: giant tobacco, adult: aphid, 9: haributirijaari, 10: Chorange bee (larva)

動物種によって、活性油の濃度が低い場合(例えば0.3〜0.5%)に行動抑制効果が不充分な例や、逆に濃度が高過ぎる場合(3%以上)には死亡する例もみられるが、いずれの種においても、比較的幅広い濃度範囲に亘って充分な抑制効果が認められる。   Cases where the action control effect is insufficient when the concentration of the active oil is low (for example, 0.3 to 0.5%) depending on the animal species, or conversely, death occurs when the concentration is too high (over 3%) However, in any species, a sufficient inhibitory effect is recognized over a relatively wide concentration range.

表3記載の油性ベース液9番(SBO)のを用い、実施例5と同様の方法で、活性油(B)の配合量(%)が3,5,10,20,30,50の油性液試料を各100g調製した。次いで、実施例9と同様の方法で油性スプレー試料を作製した。25℃に設定した室内で、それらのスプレーを以下の10種類の無脊椎動物に対して約30cmの距離から2秒間噴射して、その後の行動を観察した。各動物種はそれぞれ20匹の個体を使用し、正常な飛翔ができない場合、または自身の体長の約5倍以上の距離を移動できない場合を行動抑制効果あり、と判定した。3分以内に行動抑制が見られた個体の数と、それら個体の行動抑制時間(分)の平均値(括弧内に記載)を表8に示した(但し、120分を超える場合は、一律に120とした)。尚、試料によっては死亡個体が生じたが、その場合にはカギ括弧内に死亡した個体数を示した。1:チャドクガ(終齢幼虫),2:ジョロウグモ(1cm前後),3:オオスズメバチ,4:ガガイモハムシ,5:オンブバッタ,6:アカイエカ,7:トビズムカデ(8cm前後),8:クロゴキブリ,9:ナガメ,10:コナカイガラムシ
Oily base solution No. 9 (SBO) listed in Table 3 was used in the same manner as in Example 5, and the active oil (B) content (%) was 3, 5, 10, 20, 30, 50. 100 g of each liquid sample was prepared. Subsequently, the oil-based spray sample was produced by the same method as Example 9. In a room set at 25 ° C., these sprays were sprayed from the distance of about 30 cm to the following 10 invertebrates for 2 seconds, and the subsequent behavior was observed. Each animal species used 20 individuals, and when it was not possible to fly normally, or when it was not able to move a distance of about 5 times or more of its own body length, it was determined that there was an action suppressing effect. Table 8 shows the number of individuals in which behavioral inhibition was observed within 3 minutes and the average value (in parentheses) of behavioral inhibition time (minutes) of those individuals (exceeding 120 minutes is uniform) 120). Depending on the sample, dead individuals were generated. In that case, the number of dead individuals is shown in the brackets. 1: Chadokuga (final instar larvae), 2: Giant spider (around 1 cm), 3: Greater hornet, 4: Potato moth beetle, 5: Ombutatta, 6: Akaeka, 7: Tobism cadet (around 8 cm), 8: Black cockroach, 9: Sloth , 10: Scaraba beetle

活性油を油性液にした場合は高濃度の配合が可能となり、対象とし得る動物種の種類も増えるが、全体としては実施例10と類似した傾向がみられ、幅広い濃度範囲に亘って充分な行動抑制効果が認められる。これらのことから本発明の組成物は、非常に多くの種類の陸生無脊椎動物に対して、有用な行動抑制剤として使用し得ることが分かる。   When an active oil is used as an oily liquid, a high concentration can be blended, and the types of animal species that can be targeted also increase. However, as a whole, a tendency similar to that in Example 10 is observed, and it is sufficient over a wide concentration range. A behavioral inhibitory effect is observed. From these facts, it can be seen that the composition of the present invention can be used as a useful behavior inhibitor for a great variety of terrestrial invertebrates.

活性油C,D,Eのいずれかを含む水性乳化液用ベース液及び油性ベース液を用いて、それぞれ実施例10及び11と同様の試験試料を調製し、また同様の条件下で、各試料について5種類の動物に対する行動抑制効果を調べた。乳化液用ベース液としては、表2記載の11番(活性油C)、14番(活性油D)及び20番(活性油E)を用いた(各活性油の配合濃度は実施例10と同様の0.3〜10%の6種類)。一方、油性ベース液(ケロシン使用)については表3記載の11番(活性油C)、16番(活性油D)及び18番(活性油E)を用いた(各活性油の配合濃度は実施例11と同様の3〜50%の6種類)。試験の結果に基づき、それぞれの試料及び動物種について、充分な行動抑制効果を発揮するための、活性油の適切な配合濃度の範囲(%)を表9に示した。1:バラミドリアブラムシ,2:キイロアシナガバチ,3:ウリキンウワバ(終齢幼虫)4:ヒメスズメバチ,5:チョウバエ,6:ルリチュウレンジ(幼虫),7:ハエヤドリアシブトコバチ,8:シマサシガメ,9:オオスカシバ(終齢幼虫),10:エンマコオロギ
Test samples similar to those in Examples 10 and 11 were prepared using an aqueous emulsion base solution and an oily base solution containing any of the active oils C, D, and E, respectively. About 5 types of animals, the behavior inhibitory effect was investigated. As the base solution for the emulsified liquid, No. 11 (active oil C), No. 14 (active oil D) and No. 20 (active oil E) shown in Table 2 were used. 6 types of the same 0.3 to 10%). On the other hand, No. 11 (active oil C), No. 16 (active oil D) and No. 18 (active oil E) listed in Table 3 were used for oily base liquid (using kerosene) (the concentration of each active oil was determined). 6 to 3 to 50% as in Example 11). Based on the results of the test, Table 9 shows the range (%) of the appropriate blending concentration of the active oil for exhibiting a sufficient behavior suppressing effect for each sample and animal species. 1: Baramidria beetle, 2: Yellow-winged bee, 3: Urikinawawa (final instar larvae): 4: Hornet wasp, 5: Butterfly fly, 6: Rurichu range (larvae), 7: Fly-wing beetle, 8: Shikasugagame, 9 : Ooskashiba (last-instar larvae), 10: Enma cricket

活性油C,D,Eに関してもA,Bと類似の行動抑制効果がみられたが、CとEについては、動物種によってはややより緩和な作用を示すことが分かった。しかしEでは他の活性油に比べて、概して行動抑制時間が長くなる傾向がみられた。   The active oils C, D, and E were also found to have a behavior suppressing effect similar to that of A and B, but C and E were found to exhibit a slightly more relaxed action depending on the animal species. However, in E, there was a tendency that the action suppression time was generally longer than that of other active oils.

各活性油について、水性乳化液用ベース液及び油性ベース液を用いて、それぞれ実施例4及び実施例5と同様の方法で試験試料を調製した。乳化液用ベース液としては、表2記載の4番(活性油A)、7番(活性油B)、9番(活性油C)、16(活性油D)及びを19番(活性油E)を用い、各活性油の配合濃度はいずれも0.5%とした。一方、油性ベース液については表3記載の4番(活性油A)、7番(活性油B)、12番(活性油C)、14(活性油D)及びを17番(活性油E)を用い、各活性油の配合濃度はいずれも5%とした。次いで、乳化液ハンドスプレー試料については、対象動物にチャコウラナメクジ(20匹)を用いて実施例7と同様の方法で、また油性ベース液試料についてはオンブバッタ(20匹)を用いて、実施例9と同様の方法で試験をおこなった。対象動物に1回塗布しても行動抑制効果がみられない場合は、3分後に再度塗布し(2回目)、もしまだ効果がみられない場合は、更に3分後に再塗布(3回目)をおこなって様子を観察し、反復塗布による効果を評価した。表10に、各塗布の後、3分以内に行動抑制が見られた個体の数を示した。
About each active oil, the test sample was prepared by the method similar to Example 4 and Example 5, respectively, using the base liquid for aqueous | water-based emulsified liquids, and an oily base liquid. As the base solution for the emulsified liquid, No. 4 (active oil A), No. 7 (active oil B), No. 9 (active oil C), 16 (active oil D) and No. 19 (active oil E) shown in Table 2 are used. ), And the blending concentration of each active oil was 0.5%. On the other hand, for the oily base liquid, No. 4 (active oil A), No. 7 (active oil B), No. 12 (active oil C), No. 14 (active oil D) and No. 17 (active oil E) described in Table 3 are used. The blending concentration of each active oil was 5%. Next, for the emulsified liquid hand spray sample, Chakoura slug (20 animals) was used as the target animal in the same manner as in Example 7, and for the oily base liquid sample, the ombatta (20 animals) was used. The test was conducted in the same manner as in Example 9. If no action-suppressing effect is observed even if applied once to the subject animal, apply again after 3 minutes (second time). If no effect is seen yet, reapply after 3 minutes (third time). Was observed to observe the state, and the effect of repeated application was evaluated. Table 10 shows the number of individuals whose behavior was suppressed within 3 minutes after each application.

動物種によっては、あるいは活性油の濃度がやや不充分な場合には、複数回の塗布をおこなっても、まだ充分な行動抑制効果のみられない場合(表下段)もあるが、塗布回数の増加に伴って抑制効果も増大していることから、反復塗布の効果は明瞭に認められる。更に、多くの実験により、この反復塗布法は他のナメクジやバッタに加えて、ムカデ、クモ、ハチ、カ、ゴキブリ、カメムシ、コナジラミ、チャタテムシ、ノミ、アザミウマ、ヒル、ハムシ、ハバチ、チョウ目幼虫、同成虫、ダニ、ハダニ、ハエ、アブラムシ、アリ、シロアリ、カイガラムシ、ウンカ、トンボ、テントウムシ、カマキリ、シラミ、セミ、ホタル、カミキリムシ、コガネムシ、カワゲラ(以上、総称)など、広範囲の陸生脊椎動物に対しても有効であることを確認した。このように本発明の組成物は、塗布すべき活性油の至適成分組成や濃度が不明な動物種に対しても、行動の様子を観察しながら反復塗布することにより簡便に目的を達せられること、従ってそのことにより失敗(動物の死亡など)を回避できる可能性が高いこと、などの利点を有する。   Depending on the animal species, or if the concentration of the active oil is slightly insufficient, there may be cases where the effect of inhibiting the action is not yet sufficient even after multiple applications (lower table), but the number of applications increases. Since the inhibitory effect is also increased, the effect of repeated application is clearly recognized. In addition, many experiments have shown that this repetitive application method, in addition to other slugs and grasshoppers, includes centipedes, spiders, bees, mosquitoes, cockroaches, stink bugs, whitefly, scallops, fleas, thrips, leeches, leaf beetles, wasps, butterflies , Adults, mites, spider mites, flies, aphids, ants, termites, scale insects, planthoppers, dragonflies, ladybirds, mantis, lice, cicada, fireflies, longhorn beetles, scarab beetles, river moths, etc. It was confirmed that it was also effective. As described above, the composition of the present invention can easily achieve its purpose by repeatedly applying to the animal species whose optimum component composition or concentration of the active oil to be applied is unknown while observing the behavior. And therefore has the advantage that it is likely that failure (such as animal death) can be avoided.

実施例10〜12において、10分間以上の行動抑制効果がみられた動物に対して、正常に戻った後に、再度、同一試料を塗布したところ、大部分の動物種において、再び同様の行動抑制効果が発現することが判明した。稀に死亡する例もみられたが、多くの場合は初回塗布よりも低濃度の試料塗布で同様の抑制効果を発現した。従って、行動抑制時間を延長したい場合にも、このような追加塗布法が有効に利用し得る。   In Examples 10 to 12, when the same sample was applied again after returning to normal to animals that exhibited a behavior suppressing effect for 10 minutes or more, the same behavior suppression was again performed in most animal species. It was found that the effect was manifested. There were rare cases of death, but in many cases, the same inhibitory effect was exhibited when the sample was applied at a lower concentration than the initial application. Therefore, such an additional coating method can be used effectively when it is desired to extend the behavior suppression time.

本発明の組成物を用いて、野外でヒメスズメバチの捕獲とマーキング(表2、3番、活性油A、5%配合)及びスズムシの捕獲とマーキング(表3、10番、活性油B、15%配合)を行った。ヒメスズメバチの捕獲には捕虫網も使用したが、捕虫網を使わずとも、花などに飛来した成虫に試料を直接塗布することでも充分可能であった。また、マーキングの際にも危険性は全く無く、安心して作業を行う事ができた。一方、スズムシの捕獲にも極めて有効であり、発見した虫に的確に塗布することにより逃避行動が抑制され、容易に捕獲することが可能であった。このように本発明の組成物は、実験室内などでの使用にとどまることなく、野外においても簡便に使用できる極めて有用な行動抑制剤組成物であることが分かる。   Using the composition of the present invention, capture and marking of hornet wasp (Table 2, No. 3, active oil A, 5% blended) and sumumushi capture and marking (Table No. 3, No. 10, active oil B, 15) in the field % Formulation). Although catching nets were used to capture the hornet wasp, it was also possible to apply the sample directly to adults flying on flowers, etc., without using a catching net. Also, there was no danger at the time of marking, and I was able to work with peace of mind. On the other hand, it was extremely effective in capturing Susumu, and when it was properly applied to the found insect, escape behavior was suppressed and it was possible to capture it easily. Thus, it can be seen that the composition of the present invention is an extremely useful behavior inhibitor composition that can be easily used in the field without being limited to use in a laboratory or the like.

本発明に係る組成物は、農業・園芸分野などにおける実験材料としての害虫の研究(害虫の飼育や維持管理)に有用であり、大学や研究機関等においても広く行われている陸生無脊椎動物に関する生理、生態研究にも利用価値は高い。   The composition according to the present invention is useful for research on pests as experimental materials in the fields of agriculture and horticulture (breeding and maintenance of pests), and is widely used in universities and research institutions. It is also valuable for physiological and ecological research.

Claims (2)

シトラール−a、シトラール−b、α−テルピネオール、β−テルピネオール、γ−テルピネオール、δ−テルピネオール、α−テルピニルアセテート、β−テルピニルアセテート、γ−テルピニルアセテート、δ−テルピニルアセテートの中から選択した少なくとも1種以上の化合物から構成される活性油に、必要に応じて適量の界面活性剤を添加し、さらに必要に応じて鉱油や油脂で希釈した油性混合物、あるいは、活性油もしくは油性混合物を水中で界面活性剤を用いて調製した乳化分散液であることを特徴とする陸生無脊椎動物用行動抑制剤組成物。   Citral-a, citral-b, α-terpineol, β-terpineol, γ-terpineol, δ-terpineol, α-terpinyl acetate, β-terpinyl acetate, γ-terpinyl acetate, δ-terpinyl An active oil composed of at least one compound selected from acetate is added with an appropriate amount of a surfactant as necessary, and an oily mixture diluted with mineral oil or fat as necessary, or active A behavior inhibitor composition for terrestrial invertebrates characterized by being an emulsified dispersion prepared by using a surfactant in water or an oily mixture. 活性油を0.05%以上含有することを特徴とする請求項1の陸生無脊椎動物用行動抑制剤組成物。 The action inhibitor composition for terrestrial invertebrates according to claim 1, comprising 0.05% or more of active oil.
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WO2020170843A1 (en) * 2019-02-21 2020-08-27 アース製薬株式会社 Carnivorous wasp insecticide

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JPH1160421A (en) * 1997-08-26 1999-03-02 Shigeharu Inoue Insect pest-controlling agent
JP2001163715A (en) * 1999-12-07 2001-06-19 Earth Chem Corp Ltd Expellant for gastropod

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JPH1160421A (en) * 1997-08-26 1999-03-02 Shigeharu Inoue Insect pest-controlling agent
JP2001163715A (en) * 1999-12-07 2001-06-19 Earth Chem Corp Ltd Expellant for gastropod

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* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
WO2020170843A1 (en) * 2019-02-21 2020-08-27 アース製薬株式会社 Carnivorous wasp insecticide
JP7364314B2 (en) 2019-02-21 2023-10-18 アース製薬株式会社 carnivorous bee repellent

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