JP2003026507A - Exterminator agent against harmful gastropods and method for exterminating the harmful gastropods - Google Patents
Exterminator agent against harmful gastropods and method for exterminating the harmful gastropodsInfo
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- JP2003026507A JP2003026507A JP2001215084A JP2001215084A JP2003026507A JP 2003026507 A JP2003026507 A JP 2003026507A JP 2001215084 A JP2001215084 A JP 2001215084A JP 2001215084 A JP2001215084 A JP 2001215084A JP 2003026507 A JP2003026507 A JP 2003026507A
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- Japan
- Prior art keywords
- harmful
- gastropods
- methylphenol
- isopropyl
- cymene
- Prior art date
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Abstract
Description
【０００１】[0001]
【発明の属する技術分野】この発明は、腹足類、特に有
用作物に被害を与えるナメクジ、ウスカワマイマイ、カ
タツムリ、スクミリンゴガイ等の有害腹足類の殺滅剤に
関する。BACKGROUND OF THE INVENTION 1. Field of the Invention The present invention relates to a killing agent for harmful gastropods such as slugs, Uskawamaimai, snails and snail apple snails which damage gastropods, particularly useful crops.
【０００２】[0002]
【従来の技術及び発明が解決しようとする課題】ナメク
ジ、ウスカワマイマイ、カタツムリ等の軟体動物は、畑
地、温室、庭園等のいたるところに出没して、果樹、蔬
菜、花き等の有用作物を食害し多大な被害をもたらすこ
とはよく知られている。2. Description of the Related Art Molluscs such as slugs, Uskawamai, and snails appear and disappear everywhere in fields, greenhouses, gardens, etc. to produce useful crops such as fruit trees, vegetables and flowers. It is well known that eating damage causes a great deal of damage.
【０００３】これらを駆除するための駆除剤としては、
従来から、メタアルデヒド製剤が誘引性毒餌として使用
されている。しかし、この製剤は、充分な効果を発揮し
ているとはいえず、また、速効的な作用性に劣る欠点が
ある。As a disinfecting agent for exterminating these,
Traditionally, methaaldehyde formulations have been used as attractive bait. However, it cannot be said that this preparation exerts a sufficient effect, and there is a drawback in that it is inferior in a quick-acting action.
【０００４】また、上記以外の駆除剤として、ヒノキチ
オールや、メントール等のテルペン類も忌避剤としての
利用が期待されている。しかし、殺滅活性の面で難があ
り、一般に普及していないのが現状である。In addition to the above, terpenes such as hinokitiol and menthol are also expected to be used as repellents as repellents. However, there is a difficulty in killing activity, and the current situation is that it is not widely used.
【０００５】一方、スクミリンゴガイは、水稲、蓮根等
の農作物を食害し、最近はその被害が増大している。こ
の防除に関して有効な手段が無いのが現状である。[0005] On the other hand, the Spodoptera liturai feeds on crops such as paddy rice and lotus root, and the damage has been increasing recently. At present, there is no effective means for this control.
【０００６】そこでこの発明は、ナメクジ、ウスカワマ
イマイ、カタツムリ、スクミリンゴガイ等の有害腹足類
に対し、有効にかつ速効的に殺滅効果を発揮する殺滅剤
を提供することを目的とする。[0006] Therefore, an object of the present invention is to provide a killing agent that effectively and quickly exerts a killing effect on harmful gastropods such as slugs, Uskawamai, snails, and snail apple snails.
【０００７】[0007]
【課題を解決するための手段】この発明は、シメン系化
合物を含有する殺滅剤を用いることにより上記の課題を
解決したのである。The present invention has solved the above-mentioned problems by using a killing agent containing a cymene compound.
【０００８】この殺滅剤を用いることにより、従来駆除
が困難であったナメクジやカタツムリ等の有害腹足類に
対し速効的な殺滅効果を発揮させることができ、更にシ
ートに担持された状態でも殺滅することができる。By using this killing agent, it is possible to exert a rapid killing effect on harmful gastropods such as slugs and snails, which have been difficult to be exterminated in the past. Can be destroyed.
【０００９】[0009]
【発明の実施の形態】以下において、この発明について
詳細に説明する。この発明にかかる有害腹足類の殺滅剤
は、シメン系化合物を含有するものである。BEST MODE FOR CARRYING OUT THE INVENTION The present invention will be described in detail below. The harmful gastropod killing agent according to the present invention contains a cymene compound.
【００１０】上記有害腹足類とは、有用作物に被害を与
える腹足類をいい、例えば、コウラナメクジ科（Limaci
dae）に属するコウラナメクジ、チャコウラナメクジ、
ノナメクジ等、ナメクジ科（Philomycidae）に属するナ
メクジ、ヤマナメクジ等、ニワコウラナメクジ科（Mila
cidae）等に属するニワコウラナメクジ等のナメクジ
類、オカモノアラガイ科（Succineidae）に属するオカ
モノアラガイ類、アフリカマイマイ科（Achatinidae）
に属するアフリカマイマイ、オナジマイマイ科（Bradyb
aenidae）に属するウスカワマイマイ等のカタツムリ
類、更には、スクミリンゴガイ（ジャンボタニシ）等を
挙げることができる。The above-mentioned harmful gastropods refer to gastropods that damage useful crops, for example, Lamiciaceae (Limaci).
dae)
Slugs belonging to the slug family (Philomycidae), including slugs, slugs, slugs, etc.
cidae) and other slugs such as slugs, etc., Squid snails belonging to the family Succineidae, Scots snails (Achatinidae)
African snails belonging to the family
aenidae) and other snails such as Uskawa maimai, and further, the snail apple snail (jumbo snail) and the like.
【００１１】上記シメン系化合物としては、カルバクロ
ール（５−イソプロピル−２−メチルフェノール）、３
−イソプロピル−５−メチルフェノール、２−イソプロ
ピル−６−メチルフェノール、２−イソプロピル−５−
メチルフェノール、２−イソプロピル−４−メチルフェ
ノール、４−イソプロピル−３−メチルフェノール、４
−イソプロピル−２−メチルフェノール、３−イソプロ
ピル−４−メチルフェノール、２−イソプロピル−３−
メチルフェノール、３−イソプロピル−２−メチルフェ
ノール、ｏ−チモチン酸、ｐ−チモチン酸、ｏ−チモー
ルアルデヒド、ｐ−チモールアルデヒド、ｐ−ニトロソ
チモール、ｐ−ニトロチモール、ｐ−アミノチモール、
チモールハイドロキノン、チモキノン、４−クロルチモ
ール、４−ブロムチモール、４−ヨードチモール、チモ
ールブルー、チモールフタレイン、ブロモチモールブル
ー等の水酸基を有するシメン系化合物、その他、ｏ−シ
メン、ｍ−シメン、ｐ−シメン、２−ブロモ−ｐ−シメ
ン、塩酸モキシシリト、５−ｐ−シメン［（３−ピペリ
ジノ）ブロボキシ］誘導体等があげられる。Examples of the cymene compound include carvacrol (5-isopropyl-2-methylphenol), 3
-Isopropyl-5-methylphenol, 2-isopropyl-6-methylphenol, 2-isopropyl-5
Methylphenol, 2-isopropyl-4-methylphenol, 4-isopropyl-3-methylphenol, 4
-Isopropyl-2-methylphenol, 3-isopropyl-4-methylphenol, 2-isopropyl-3-
Methylphenol, 3-isopropyl-2-methylphenol, o-thymotic acid, p-thymotic acid, o-thymol aldehyde, p-thymol aldehyde, p-nitrosothymol, p-nitrothymol, p-aminothymol,
A cymene compound having a hydroxyl group such as thymol hydroquinone, thymoquinone, 4-chlorothymol, 4-bromothymol, 4-iodothymol, thymol blue, thymol phthalein, and bromothymol blue, and others, o-cymene, m-cymene, p -Cymene, 2-bromo-p-cymene, moxicilito hydrochloride, 5-p-cymene [(3-piperidino) broboxy] derivative and the like.
【００１２】これらの中でも、水酸基を有するシメン系
化合物が好ましく、４−イソプロピル−３−メチルフェ
ノール、２−イソプロピル−５−メチルフェノールがよ
り好ましい。Of these, the cymene compound having a hydroxyl group is preferable, and 4-isopropyl-3-methylphenol and 2-isopropyl-5-methylphenol are more preferable.
【００１３】この発明にかかる殺滅剤は、そのものを使
用してもよく、メタノール、エタノール等のアルコール
等の溶媒に溶かし使用してもよく、乳剤、粉剤、粒剤、
水和剤、液剤、水溶剤、ペースト、あるいは発泡剤、エ
アゾール、マイクロカプセル剤等に製剤化して、使用し
てもよい。また、補助剤、例えば、展着剤、乳化剤、湿
展剤等の界面活性剤を混用して効果の確実性を期するこ
ともむろん好ましい。The killing agent according to the present invention may be used as it is, or may be used by dissolving it in a solvent such as alcohol such as methanol or ethanol, and may be used as an emulsion, powder, granule,
It may be used by formulating it into a wettable powder, a liquid preparation, a water solvent, a paste, a foaming agent, an aerosol, a microcapsule or the like. It is also preferable to use an auxiliary agent, for example, a surface active agent such as a spreading agent, an emulsifying agent, or a wetting agent in order to ensure the certainty of the effect.
【００１４】目的によってこれらの化合物に他の殺菌
剤、殺虫剤、除草剤、忌避剤、又は肥料等を混用して、
同時に施用することも可能である。また、穀類、麦皮、
蛋白質生成物、カゼイン、乾燥酵母および精油の如き天
然および合成誘引剤と組み合わせて誘引性駆除剤とする
こともできる。さらに、香料成分、酸化防止剤、光安定
剤等と組み合わせてもよい。Depending on the purpose, these compounds are mixed with other fungicides, insecticides, herbicides, repellents, fertilizers, etc.,
It is also possible to apply at the same time. Also, cereals, bark,
It may also be combined with natural and synthetic attractants such as protein products, casein, dried yeast and essential oils to provide attractive attractants. Further, it may be combined with a fragrance component, an antioxidant, a light stabilizer and the like.
【００１５】上記の他の殺菌剤としては、キタジンＰ、
チアベンダゾール等があげられ、上記忌避剤としては、
ｐ−メンタン−３，８−ジオール、２−ヒドロキシメチ
ルトリメチルシクロヘキサノール、Ｎ，Ｎ−ジエチル−
ｍ−トルアミド、ジメチルフタレート、２−エチル−
１，３−へキサンジオール、サイネピリン２２２、２，
３，４，５−ビス（Δ２−ブチレン）テトラヒドロフル
フラール、ジ−ｎ−プロピルイソシンコメロネート、ジ
−ｎ−ブチルサクシネート、２−ヒドロキシエチルオク
チルスルフィド、エンペントリン、カラン−３，４−ジ
オール等や、硫酸銅、グルコン酸銅等の銅化合物、硫酸
アルミニウム等のアルミニウム化合物等があげられる。Other bactericides mentioned above include Kitadine P,
Thiabendazole and the like, and as the above-mentioned repellent,
p-menthane-3,8-diol, 2-hydroxymethyltrimethylcyclohexanol, N, N-diethyl-
m-toluamide, dimethyl phthalate, 2-ethyl-
1,3-hexanediol, cinepyrine 222, 2,
3,4,5-bis (Δ2-butylene) tetrahydrofurfural, di-n-propylisocinchomeronate, di-n-butylsuccinate, 2-hydroxyethyloctyl sulfide, enpentrin, carane-3,4-diol, etc. And copper compounds such as copper sulfate and copper gluconate, aluminum compounds such as aluminum sulfate, and the like.
【００１６】上記の香料成分としては、オイゲノール、
シネオール、ユーカリ油、月桃油、ティーツリーオイ
ル、クローブ、メントール、アネトール、ヒノキチオー
ル、カンフル等があげられる。As the above-mentioned fragrance ingredients, eugenol,
Examples include cineol, eucalyptus oil, moon peach oil, tea tree oil, clove, menthol, anethole, hinokitiol, camphor and the like.
【００１７】また、上記の酸化防止剤や光安定剤として
は、ブチルヒドロキシアニソール、ジブチルヒドロキシ
トルエン、没食子酸プロピル、トコフェロール、ガンマ
ーオリザノール、アスコルビン酸、カプサイシン、トリ
フェニルフォスファイト、ジフェニルイソデシルホスフ
ァイト、ｐ−ｔ−ブチルフェニルサリシレート等があげ
られる。The above-mentioned antioxidants and light stabilizers include butylhydroxyanisole, dibutylhydroxytoluene, propyl gallate, tocopherol, gamma-oryzanol, ascorbic acid, capsaicin, triphenylphosphite, diphenylisodecylphosphite, Examples thereof include p-t-butylphenyl salicylate.
【００１８】この発明にかかる有害腹足類の殺滅剤の使
用法としては、直接法と間接法があげられる。上記直接
法としては、上記殺滅剤を上記のように溶剤に溶解又は
製剤化し、これをスプレー散布する散布法等があげられ
る。さらに、農業栽培場面においては、土壌にあらかじ
め混和し、土壌中で駆除する処理方法もあげられる。ま
た、上記間接法としては、上記殺滅剤又は溶剤による溶
解物をシート等に担持させて腹足類の通路に置く方法等
があげられる。上記のシート等を用いる場合は、そのシ
ートに侵入する有害腹足類を殺滅することができる。Examples of the method of using the harmful gastropod killing agent according to the present invention include a direct method and an indirect method. Examples of the direct method include a spraying method in which the above-mentioned disinfectant is dissolved or formulated in a solvent as described above, and this is sprayed. Furthermore, in the case of agricultural cultivation, there is also a treatment method in which it is mixed with soil in advance and exterminated in the soil. In addition, examples of the indirect method include a method in which a dissolved product of the killing agent or the solvent is supported on a sheet or the like and placed in a passage of a gastropod. When the above sheet or the like is used, harmful gastropods that enter the sheet can be killed.
【００１９】上記の担持方法としては、特に限定されな
いが、熱がかかると、上記シメン系化合物の分解や揮散
を招く恐れがあるので、低温での方法が好ましい。この
ような方法としては、上記溶解物をシート上に塗布した
り、シートを上記溶解物に浸漬したりする等の塗工法、
または、シート等に練り込む方法等があげられる。The supporting method is not particularly limited, but a low temperature method is preferable because it may cause decomposition or volatilization of the cymene compound when heated. As such a method, a coating method such as coating the melt on a sheet or dipping the sheet in the melt,
Alternatively, a method of kneading into a sheet or the like may be used.
【００２０】上記シート等の材質は、特に制限されるも
のではなく、ポリエチレン、ポリプロピレン等のポリオ
レフィン、ポリエステル、ポリアミド、ポリ乳酸等の合
成樹脂や、綿、紙、セルロース等の天然樹脂等があげら
れる。The material of the sheet or the like is not particularly limited, and examples thereof include polyolefins such as polyethylene and polypropylene, synthetic resins such as polyester, polyamide and polylactic acid, and natural resins such as cotton, paper and cellulose. .
【００２１】上記の殺滅剤中の上記シメン系化合物の配
合割合は、所望に応じて任意の割合とすることができ
る。上記の散布法を採用する場合、上記シメン系化合物
の濃度としては、０．０２〜２０重量％がよく、０．１
〜５重量％が好ましい。さらに、土壌混和の場合は、有
害腹足類の密度により様々であるが、１〜１００ｇ／ｍ
2が好ましい。また、上記のシートに担持する方法を採
用する場合、上記シメン系化合物の濃度は、特に限定さ
れないが、０．０５〜５０ｇ／ｍ2が好ましい。上記の
各範囲の下限を下回ると、殺滅効果が不十分となる場合
がある。一方、上記の各範囲の上限を上回ると、草花等
への薬害が起こる場合がある。The content ratio of the above-mentioned cymene compound in the above-mentioned disinfectant can be any ratio as desired. When the above spraying method is adopted, the concentration of the cymene compound is preferably 0.02 to 20% by weight,
-5% by weight is preferred. Furthermore, in the case of soil admixture, it varies depending on the density of harmful gastropods, but 1 to 100 g / m
2 is preferred. When the method of supporting on the sheet is adopted, the concentration of the cymene compound is not particularly limited, but is preferably 0.05 to 50 g / m 2 . Below the lower limit of each of the above ranges, the killing effect may be insufficient. On the other hand, if the upper limit of each of the above ranges is exceeded, phytotoxicity to flowers may occur.
【００２２】[0022]
【実施例】以下に実施例及び比較例をあげてこの発明を
さらに具体的に説明する。
（実施例１）以下、本発明を実施例をあげてより詳細に
説明する。２-イソプロピル-５-メチルフェノールを所
定濃度になるように４０％エタノールに溶解し、供試溶
液とした。これを１滴（０．０５ｍｌ）、ナメクジ（チ
ャコウラナメクジ）に滴下し、致死に至る時間を測定し
た。また、同様にカタツムリ（クチベニマイマイ）に滴
下し、致死に至る時間を測定した。その結果を表１に示
す。EXAMPLES The present invention will be described more specifically with reference to Examples and Comparative Examples below. (Example 1) Hereinafter, the present invention will be described in more detail with reference to examples. 2-Isopropyl-5-methylphenol was dissolved in 40% ethanol to a predetermined concentration to prepare a test solution. One drop (0.05 ml) of this was added dropwise to slugs (Chlorophora slugs), and the time to lethality was measured. Similarly, it was added dropwise to a snail (Cutebenima myima) and the time to lethality was measured. The results are shown in Table 1.
【００２３】（実施例２）２-イソプロピル-５-メチル
フェノール０．５ｇと界面活性剤 ニューカルゲン２１
１９Ｋ（竹本油脂製）１．５ｇを混合溶解させた後、水
を９８ｇ加え、０．５％水性剤として、水性の供試溶液
とした。これを実施例１と同様の方法でナメクジへの効
果を判定した。また、同様にカタツムリ（クチベニマイ
マイ）に滴下し、致死に至る時間を測定した。その結果
を表１に示す。(Example 2) 0.5 g of 2-isopropyl-5-methylphenol and the surfactant Newcalgen 21
After 1.5 g of 19K (manufactured by Takemoto Yushi Co., Ltd.) was mixed and dissolved, 98 g of water was added to prepare an aqueous test solution as a 0.5% aqueous agent. The effect on slugs was determined by the same method as in Example 1. Similarly, it was added dropwise to a snail (Cutebenima myima) and the time to lethality was measured. The results are shown in Table 1.
【００２４】（実施例３）４−イソプロピル−３−メチ
ルフェノールを所定濃度になるように４０％エタノール
に溶解し、供試溶液とした。これを実施例１と同様の方
法でナメクジへの効果を判定した。また、同様にカタツ
ムリ（クチベニマイマイ）に滴下し、致死に至る時間を
測定した。その結果を表１に示す。(Example 3) 4-isopropyl-3-methylphenol was dissolved in 40% ethanol to a predetermined concentration to prepare a test solution. The effect on slugs was determined by the same method as in Example 1. Similarly, it was added dropwise to a snail (Cutebenima myima) and the time to lethality was measured. The results are shown in Table 1.
【００２５】（比較例１）忌避効果が高いとされている
ヒノキチオールを所定濃度になるように４０％エタノー
ルに溶解し、供試溶液とした。これを実施例１と同様の
方法でナメクジへの効果を判定した。その結果を表１に
示す。また、同様にカタツムリ（クチベニマイマイ）に
滴下し、致死に至る時間を測定した。その結果を表１に
示す。Comparative Example 1 Hinokitiol, which is said to have a high repellent effect, was dissolved in 40% ethanol to a predetermined concentration to prepare a test solution. The effect on slugs was determined by the same method as in Example 1. The results are shown in Table 1. Similarly, it was added dropwise to a snail (Cutebenima myima) and the time to lethality was measured. The results are shown in Table 1.
【００２６】（比較例２）忌避効果が高いとされている
メントールを所定濃度になるように４０％エタノールに
溶解し、供試溶液とした。これを実施例１と同様の方法
でナメクジへの効果を判定した。また、同様にカタツム
リ（クチベニマイマイ）に滴下し、致死に至る時間を測
定した。その結果を表１に示す。(Comparative Example 2) Menthol, which is said to have a high repellent effect, was dissolved in 40% ethanol to a predetermined concentration to prepare a test solution. The effect on slugs was determined by the same method as in Example 1. Similarly, it was added dropwise to a snail (Cutebenima myima) and the time to lethality was measured. The results are shown in Table 1.
【００２７】（比較例３）誘引駆除剤として実用化され
ているメタアルデヒドを所定濃度になるように水と界面
活性剤で分散させ、供試溶液とした。これを実施例１と
同様の方法でナメクジへの効果を判定した。Comparative Example 3 A test solution was prepared by dispersing methaaldehyde, which is practically used as an attracting and exterminating agent, with water and a surfactant so as to have a predetermined concentration. The effect on slugs was determined by the same method as in Example 1.
【００２８】[0028]
【表１】 [Table 1]
【００２９】（実施例４）２-イソプロピル-５-メチル
フェノールをエタノールに溶解し、径９ｃｍの濾紙上に
所定濃度になるよう均一に塗布し、常温で乾燥させた。
この濾紙の中心にナメクジ（チャコウラナメクジ）を置
いた後、ナメクジが濾紙上に停止とどまり、そのまま死
んでいく塗布最低濃度（以下、「制止致死濃度」と記載
する。）を求めた。この評価は、塗布したシート内への
ナメクジ侵入阻止活性の評価を目的に行ったものであ
る。その結果を表２に示す。Example 4 2-Isopropyl-5-methylphenol was dissolved in ethanol, uniformly applied on a filter paper having a diameter of 9 cm to a predetermined concentration, and dried at room temperature.
After placing a slug (Pleurotus slug) on the center of this filter paper, the minimum application concentration (hereinafter referred to as "inhibitory lethal concentration") at which the slug remained on the filter paper and died as it was was determined. This evaluation was carried out for the purpose of evaluating the activity of inhibiting slug entry into the coated sheet. The results are shown in Table 2.
【００３０】（実施例５）４−イソプロピル−３−メチ
ルフェノールを用いた以外は、実施例４と同様の方法で
評価した。その結果を表２に示す。(Example 5) Evaluation was made in the same manner as in Example 4 except that 4-isopropyl-3-methylphenol was used. The results are shown in Table 2.
【００３１】（比較例４）ヒノキチオールを用いた以外
は、実施例４と同様の方法で評価した。その結果を表２
に示す。(Comparative Example 4) Evaluation was made in the same manner as in Example 4 except that hinokitiol was used. The results are shown in Table 2.
Shown in.
【００３２】（比較例５）メタアルデヒドをクロロホル
ムに溶解したものを用いた以外は、実施例４と同様の方
法で評価した。その結果を表２に示す。(Comparative Example 5) Evaluation was made in the same manner as in Example 4 except that a solution of metaaldehyde dissolved in chloroform was used. The results are shown in Table 2.
【００３３】[0033]
【表２】 [Table 2]
【００３４】[0034]
【発明の効果】この発明にかかる有害腹足類の殺滅剤
は、シメン系化合物を用いるので、従来駆除が困難であ
ったナメクジやカタツムリ等の有害腹足類に対し速効的
に殺滅効果を示すことができる。INDUSTRIAL APPLICABILITY Since the harmful gastropod killing agent according to the present invention uses a cymene compound, it can quickly and rapidly kill harmful gastropods such as slugs and snails which have been difficult to be exterminated. it can.
【００３５】また、シートに担持させた状態でも殺滅す
ることができる。Further, the sheet can be killed even when it is carried on the sheet.
───────────────────────────────────────────────────── フロントページの続き (72)発明者 坂田 豪 大阪市西淀川区中島２丁目６番11号 大阪 化成株式会社本社工場内 Ｆターム(参考） 4H011 AC01 BA01 BB03 BC03 DA07 DA13 DC05 DC10 DD04 ─────────────────────────────────────────────────── ─── Continued front page (72) Inventor Go Sakata 2-6-11 Nakajima, Nishiyodogawa-ku, Osaka Kasei Co., Ltd. Headquarters factory F-term (reference) 4H011 AC01 BA01 BB03 BC03 DA07 DA13 DC05 DC10 DD04
Claims (5)
殺滅剤。1. A pesticide for harmful gastropods containing a cymene compound.
−５−メチルフェノール又は４−イソプロピル−３−メ
チルフェノールである請求項１に記載の有害腹足類の殺
滅剤。2. The insecticide for harmful gastropods according to claim 1, wherein the cymene compound is 2-isopropyl-5-methylphenol or 4-isopropyl-3-methylphenol.
滅剤を有害腹足類に直接スプレー散布する有害腹足類の
殺滅方法。3. A method for killing harmful gastropods, which comprises spraying the harmful gastropod killing agent according to claim 1 or 2 directly onto the harmful gastropods.
滅剤を土壌に混和する有害腹足類の殺滅方法。4. A method for killing harmful gastropods, which comprises mixing the harmful gastropod killing agent according to claim 1 or 2 with soil.
滅剤をシートに担持させ、上記シートに侵入する有害腹
足類を殺滅する有害腹足類の殺滅方法。5. A method for killing harmful gastropods, wherein a harmful gastropod killing agent according to claim 1 or 2 is carried on a sheet, and harmful gastropods that enter the sheet are killed.
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| JP2011023013A Division JP2011105758A (en) | 2011-02-04 | 2011-02-04 | Gastropod pest control agent and control method |
| JP2011023029A Division JP2011105759A (en) | 2011-02-04 | 2011-02-04 | Gastropod pest control agent and control method |
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Cited By (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JP2011105759A (en) * | 2011-02-04 | 2011-06-02 | Osaka Kasei Kk | Gastropod pest control agent and control method |
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|---|---|---|---|---|
| JPH01294601A (en) * | 1988-05-20 | 1989-11-28 | Mikasa Kagaku Kogyo Kk | Repelling composition against harmful animal |
| JPH0267202A (en) * | 1988-09-01 | 1990-03-07 | Takara Kosan Kk | Mothproofing molded product |
| JPH04288003A (en) * | 1991-03-14 | 1992-10-13 | Mikasa Kagaku Kogyo Kk | Harmful animal repelling composition |
| JPH04327511A (en) * | 1991-04-24 | 1992-11-17 | Matsushita Electric Works Ltd | Antimicrobial agent for electric razor |
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| JP2000106865A (en) * | 1998-07-29 | 2000-04-18 | Aventis Behring Gmbh | Method for cleanup of viral contamination and agent therefor |
| JP2001163715A (en) * | 1999-12-07 | 2001-06-19 | Earth Chem Corp Ltd | Expellant for gastropod |
| JP2001302412A (en) * | 2000-04-19 | 2001-10-31 | Fumakilla Ltd | Expellant for mollusc belonging to gastropoda |
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| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JP2011105759A (en) * | 2011-02-04 | 2011-06-02 | Osaka Kasei Kk | Gastropod pest control agent and control method |
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