JPH02111706A - Soil-treatment insecticide for agricultural and horticultural use - Google Patents
Soil-treatment insecticide for agricultural and horticultural useInfo
- Publication number
- JPH02111706A JPH02111706A JP63263517A JP26351788A JPH02111706A JP H02111706 A JPH02111706 A JP H02111706A JP 63263517 A JP63263517 A JP 63263517A JP 26351788 A JP26351788 A JP 26351788A JP H02111706 A JPH02111706 A JP H02111706A
- Authority
- JP
- Japan
- Prior art keywords
- soil
- agricultural
- beetle
- parts
- compound
- Prior art date
- Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
- Granted
Links
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- 239000002917 insecticide Substances 0.000 title claims abstract description 23
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- 239000008158 vegetable oil Substances 0.000 description 1
- 125000000391 vinyl group Chemical group [H]C([*])=C([H])[H] 0.000 description 1
- 229920002554 vinyl polymer Polymers 0.000 description 1
- 239000004563 wettable powder Substances 0.000 description 1
- 239000008096 xylene Substances 0.000 description 1
Landscapes
- Agricultural Chemicals And Associated Chemicals (AREA)
Abstract
Description
【発明の詳細な説明】
〔産業上の利用分野〕
本発明は、ジメチ/L/(4−エトキシフェニ/v )
(3−(3−フェノキシ−4−フルオロフェニル)プ
ロピ/L/ノンフンとオクタクロロジプロピルエーテル
を含有することを特徴とする農園芸用土壌処理殺虫剤に
関する。[Detailed Description of the Invention] [Industrial Application Field] The present invention provides dimethy/L/(4-ethoxypheny/v)
(Regarding an agricultural and horticultural soil treatment insecticide characterized by containing 3-(3-phenoxy-4-fluorophenyl)propyl/L/nonfun and octachlorodipropyl ether.
近年、コガネムシ類、ネキリムシ類、ハムシ類などやあ
るいはシパットガ、シパオサゾウムシなどの害虫、すな
わち、土壌環境に永続的あるいは一時的に生息し、そこ
で作物あるいは草木になんらかの加害活動を行っている
昆虫等の小動物群(以後土壌害虫と称す)の被害が、全
国各地の農耕地、ゴルフ場、あるいは森林で増大し問題
となっているが、これらの害虫は、土中にあって、直接
行動や習性を観察できず、害虫個体数や被害の調査が容
易でないこと、しかも発育期が長く飼育が困難なことな
どから生態の究明が十分でなく、依然効果的かつ安定し
た防除法が確立されていないのが現状である。In recent years, insect pests such as scarab beetles, cutworms, potato beetles, sipat moths, and sipata weevils, in other words, small animals such as insects that live permanently or temporarily in the soil environment and carry out some kind of harmful activity on crops or plants, have been introduced. The damage caused by these pests (hereinafter referred to as soil pests) is increasing and becoming a problem in agricultural land, golf courses, and forests across the country. Because it is not easy to investigate the pest population and damage, and the growth period is long and breeding is difficult, the ecology has not been sufficiently investigated, and effective and stable control methods have not yet been established. This is the current situation.
一般に土壌害虫を防除するにあたっては、二つの方法す
なわち植え付は直前に、あらかじめ殺虫剤を畦内に土壌
混入しておき、生息あるいは発生してくる幼虫をそれに
よって殺虫して防除しようとする方法と、産卵に飛来す
る成虫とふ化後まもない若齢幼虫を対象に畦上に散布し
て防除する方法がとられ、いずれの場合も、カルボヌル
ファン、NAC等のカーバメート系殺虫剤や、あるいは
ダイアジノン、イソキサチオン、エチμチオメトン、M
PP 、アセフェ−)、DEP等の有機リン系殺虫剤の
粉剤1粒剤、ベイト剤などが主に使用されているが、こ
れらの薬剤は、土壌中の安定性に欠け、史に、物性上土
壌中の有機物や土性等に強く影響を受けるためその防除
効果は極めて不安定となっている。In general, there are two methods for controlling soil pests: one is to mix insecticides into the soil in the ridges immediately before planting, and use this to kill the larvae that live or emerge. The method of controlling these insects by spraying them on the ridges is to target the adult insects that fly to spawn and the young larvae that have just hatched.In either case, carbamate insecticides such as carbonurphan and NAC, or Diazinon, isoxathion, ethium thiometone, M
Powders and baits of organophosphorus insecticides such as PP, Acephe) and DEP are mainly used, but these agents lack stability in the soil and have historically had poor physical properties. Its control effect is extremely unstable because it is strongly affected by organic matter in the soil and soil texture.
なかには、エチルチオメトンのように、植物浸透性を付
与し、土壌混和抜根から茎葉に移行して吸汗性害虫に殺
虫効果を発揮するものもあるが、薬害や作物残留の点で
問題が多い。Some of these, such as ethylthiometone, impart plant permeability and are effective against sweat-absorbing insect pests by transferring from the soil-mixed roots to the leaves, but there are many problems in terms of chemical damage and residue on crops.
また、EDB、DBCP、臭化メチル、カーバムなどの
従来の殺線虫剤も使用されているが、適用範囲が植物寄
生性土壌線虫に限られ、しかも土壌中でガスとして拡散
するため、人畜に対する毒性、刺激性あるいは作付期間
の制限等の欠点がある。Conventional nematicides such as EDB, DBCP, methyl bromide, and carbam are also used, but their applicability is limited to plant-parasitic soil nematodes, and they diffuse as gas in the soil, making them difficult to control for humans and animals. There are disadvantages such as toxicity, irritation, and limited planting period.
最近、ペルメトリン、フェンバレレートなどのビレヌロ
イド剤の適用も試みられているが、−般に土壌脱着性に
問題があって有効な手段となり得ないことが明らかとな
り、新しい防除成分の開発が切望されている。Recently, attempts have been made to apply birenuloid agents such as permethrin and fenvalerate, but it has become clear that they generally have problems with soil desorption and cannot be an effective means, and there is a strong need for the development of new pest control ingredients. There is.
本発明は、現状の種々土壌処理殺虫剤が直面する上記問
題点を克服し、土壌中の安定性にすぐれ、更に土壌脱着
性の改良によって土壌中の有機物や土性あるいけ気象条
件に影響を受けることなく安定して高い防除効果を与え
、かつ安全で薬害を生じない新しいタイプの農園芸用土
壌処理殺虫剤を提供しようとするものである。The present invention overcomes the above-mentioned problems faced by various current soil treatment insecticides, has excellent stability in soil, and furthermore has no effect on organic matter in soil, soil texture, or climatic conditions by improving soil desorption properties. The purpose of the present invention is to provide a new type of soil treatment insecticide for agriculture and horticulture that stably provides high pesticidal effects without causing harmful effects, is safe, and does not cause chemical damage.
〔問題点を解決するための手段及び作用〕本発明者ら打
t、鋭意研究を重ねた結果、ジメチ)v(4−エトキシ
フェニル)(3−(3−フェノキシ−4−フルオロフェ
ニlv)プロピ/I/1シラン(以下化合物Aと称す)
とオクタクロロジプロピルエーテ/L/(以下S−42
1と称す)を含有する農園芸用土壌処理殺虫剤が、本発
明の所期の目的を達成しえることを見い出し本発明を完
成した。[Means and effects for solving the problem] As a result of extensive research by the present inventors, we found that dimethy)v(4-ethoxyphenyl)(3-(3-phenoxy-4-fluorophenylv)propylene) /I/1 silane (hereinafter referred to as compound A)
and octachlorodipropylethe/L/(hereinafter S-42
The present invention was completed based on the discovery that a soil treatment insecticide for agricultural and horticultural use containing the compound (referred to as 1) can achieve the intended purpose of the present invention.
高い殺虫、殺ダニ活性と人畜に対する低毒性を兼備した
化合物として既に公知で(特開昭6l−87687)、
特にリン翅Hの害虫、アブラムシ類、ウンカ類等に高い
殺虫活性を有するため農園芸用分野で実用化が検討され
ているが、直翅目の害虫に対して低活性であること、ま
た土壌中有捜物に吸着されやすいことから、土壌処理殺
虫剤用途には不向きであると考えられていたものである
。It is already known as a compound that has high insecticidal and acaricidal activity and low toxicity to humans and livestock (Japanese Patent Application Laid-Open No. 61-87687).
In particular, it has high insecticidal activity against insect pests of Phylnoptera, aphids, planthoppers, etc., and its practical application in the field of agriculture and horticulture is being considered. It was thought to be unsuitable for use as a soil treatment insecticide because it is easily adsorbed by found materials.
しかるに本発明者らは、土壌害虫の生卵等を考慮した時
、土壌害虫の殺虫成分の評価としては基礎殺虫効力試験
のみでは不適切であると考え、種々の化合物について実
用的な土壌処理試崎を行ったところ化合物Aが土壌中安
定性にすぐれていることはもとより、コガネムシ類、ネ
キリムシ類等の土壌害虫に対して高い防除効果を与え、
従来のピレスロイドとは異なった挙動を示すことを見い
出した。However, when considering raw eggs of soil pests, the present inventors believe that basic insecticidal efficacy tests alone are inappropriate for evaluating insecticidal components of soil pests, and therefore conducted practical soil treatment tests for various compounds. After testing, we found that Compound A not only has excellent stability in soil, but also has a high control effect against soil pests such as scarab beetles and bed bugs.
It was discovered that it behaves differently from conventional pyrethroids.
史に本発明者らは、化合物Aが有機リン剤やカーバメー
ト剤と比べると高価な殺虫剤であることを鑑み、コスト
ダウンを図る目的で土壌処理殺虫剤をめざしたピレスロ
イド用共力剤の探索を行ったところ、化合物Aと5−4
21との組み合わせが、ピベロニルプトキサイド、サイ
ネビりン500 、MOK−264、セサミン、スルホ
キサイド、N工A−16388などの他の共力剤に比べ
て特異的に高い相乗効果を示すことを見い出し本発明を
完成するに至ったのである。In view of the fact that Compound A is an expensive insecticide compared to organic phosphorus agents and carbamate agents, the present inventors searched for a synergist for pyrethroid with the aim of reducing costs as a soil treatment insecticide. When performing this, compound A and 5-4
The combination with 21 shows a specifically high synergistic effect compared to other synergists such as piveronyl ptoxide, cynevirine 500, MOK-264, sesamin, sulfoxide, and N-A-16388. They discovered this and completed the present invention.
S−421の相乗効果の要因としては、殺虫効力の寄与
以外に土壌脱着性の改良すなわち、5−421を加える
ことによって化合物Aの土壌中の腐植物、土壌コロイド
粒子等への吸着が軽減され、その結果化合物Aの分解あ
るいは不動化が抑えられたことがあげられる。In addition to its contribution to insecticidal efficacy, the synergistic effect of S-421 is due to improved soil desorption properties, i.e., the addition of 5-421 reduces the adsorption of Compound A to humic plants, soil colloid particles, etc. in the soil. As a result, decomposition or immobilization of Compound A was suppressed.
従来、S−421などのピレスロイド用共力剤は、有効
成分の昆虫体内での代廁分解を阻害することによって共
力効果を発揮するものと考えられており、本発明が開示
する土壌脱着性の改良に基づく相乗効果は、従来知見か
らは全く想到しえないものである。Conventionally, synergists for pyrethroid such as S-421 are thought to exert a synergistic effect by inhibiting the vicariance decomposition of the active ingredient within the insect body, and the soil desorption properties disclosed in the present invention The synergistic effect based on the improvement of is completely inconceivable from conventional knowledge.
本発明土壌処理殺虫剤には、殺虫成分として化合物Aを
0.05〜80重量%含有することができ、5−421
と混合する場合高い共力効果を奏する化合物Aと8−4
21との混合比は2:1〜1:10(好ましくは]:1
〜1:5)が適当である。The soil treatment insecticide of the present invention may contain 0.05 to 80% by weight of compound A as an insecticidal component, and may contain 5-421% by weight of compound A.
Compound A and 8-4 exhibit a high synergistic effect when mixed with
The mixing ratio with 21 is 2:1 to 1:10 (preferably]:1
~1:5) is suitable.
混合比が上記の範囲をはずれると土壌中における脱着性
が改良されず、防除効果は非常に不安定となる。If the mixing ratio is outside the above range, the desorption properties in the soil will not be improved and the control effect will be extremely unstable.
本発明農園芸用土壌処理殺虫剤の剤型としては、殺虫剤
の性状、使用目的により、粉剤。The dosage form of the soil treatment insecticide for agriculture and horticulture of the present invention may be a powder, depending on the properties of the insecticide and the purpose of use.
粒剤、乳剤、水利剤、懸濁剤、ベイト剤など種々可能で
ある。Various forms such as granules, emulsions, irrigation agents, suspension agents, and bait agents are possible.
いずれの製剤も常法に従って調製することができ、固体
担体としては粘土類(カオリン。Both formulations can be prepared according to conventional methods, and the solid carrier is clay (kaolin).
クレー類など)、タルク類、その他の無機鉱物(例えば
セリサイト、硫黄粉末、活性炭。clays, etc.), talc, and other inorganic minerals (e.g. sericite, sulfur powder, activated carbon).
炭酸カルシウム、水和シリカ)、化学肥料(例えば、硫
安、リン安、硝安、尿素)などの微粉末、あるいは粒状
物があげられる。なお、粉剤については、散布時のドリ
フトを抑制し7環境汚染を防止する観点から、粒度分布
上、10ミクロン以下の微粉末を全体の20%以下にカ
ットしたもの例えばドリフトレスフレ=(DT、クレー
)類が特に有用である。Examples include fine powders or granules of calcium carbonate, hydrated silica), chemical fertilizers (e.g., ammonium sulfate, ammonium phosphorus, ammonium nitrate, urea), etc. In addition, regarding powders, from the viewpoint of suppressing drift during spraying and preventing environmental pollution, powders with particle size distribution of 10 microns or less are cut to 20% or less of the total, such as Driftless Flare = (DT, Particularly useful are clays.
液体担体としては、水、アルコ−/I/類、類書芳香族
炭化水素類えばトルエン、キンレフなど)、脂肪族炭化
水素類(例えばケロシン。Liquid carriers include water, alcohols, aromatic hydrocarbons such as toluene and Kinlev, aliphatic hydrocarbons such as kerosene.
灯油など)、エステル類、ニトリル類などが使用できる
。次に界面活性剤としてはアルキル硫酸エヌテμ類、ア
ルキルスpホン酸塩。Kerosene, etc.), esters, nitriles, etc. can be used. Next, as surfactants, alkyl sulfate NTE μ and alkyl sulfonates are used.
アルギρアリールスルホン酸塩、ポリエチレングリコー
ルエーテル類、多価アルコールエステμ類などがあげら
れる。その他適宜、カゼイン、ゼラチン、でんぷんH)
、cMc、ポリビニルアルコールなどの固着剤や分散剤
が使用される。Examples include algyl ρ aryl sulfonates, polyethylene glycol ethers, and polyhydric alcohol esters. Other appropriate casein, gelatin, starch H)
, cMc, polyvinyl alcohol, and other fixing agents and dispersants are used.
また、本発明で使用される化合物Aをマイクロカプセル
化又はサイクロデキストリン包接化することにより、あ
るいはBHT 、スミフィザーBP−101(住友化学
商品名)、植物油、界面活性剤、アルキ、It/vン酸
誘導体、グツイコール類などの安定剤を加えて化学的安
定性を増し、土壌中における残効性を高めた製剤を得る
ことも可能である。In addition, by microencapsulating or cyclodextrin inclusion of Compound A used in the present invention, BHT, Sumifizer BP-101 (Sumitomo Chemical brand name), vegetable oil, surfactant, alkyl, It/v. It is also possible to add stabilizers such as acid derivatives and gutuicols to increase chemical stability and obtain formulations with increased residual efficacy in soil.
更に本発明の組成物に、他の殺虫剤、例えばフェニトロ
チオン、イソキサチオン、MPP、アセフェート、DE
P 、ダイアジノン、エチルチオントンなどの有機リン
剤、カルポス/レフアン、NkC。Additionally, the compositions of the invention may contain other insecticides such as fenitrothion, isoxathion, MPP, acephate, DE
P, diazinon, organic phosphorus agents such as ethylthionthone, Calpos/Lefan, NkC.
MTMC、BPMO、PHCなどのカーバメート剤。Carbamate agents such as MTMC, BPMO, PHC.
ピレトリン、アレスリン、フタールスリン、フッメトリ
ン、フエノトリン、ペルメトリン、フェンバレレート、
フルパリネート、エトフエンブロックスなどの従来のピ
レスロイド系殺虫剤、カルタップ、クロルフェナミジン
、ブプロフェジンなどの殺虫剤あるいは殺ダニ剤、殺菌
剤、殺線虫剤、除草剤、昆虫成長かく乱剤、植物生長調
整剤、IIa料その他の農薬を混合することによって効
果のすぐれた多目的組成物が得られ、労力の省力化、薬
剤間の相乗効果も充分期待しえるものである。Pyrethrin, allethrin, phthalthrin, fumetrin, phenothrin, permethrin, fenvalerate,
Conventional pyrethroid insecticides such as fluparinate and etofenbrox, insecticides or acaricides such as cartap, chlorphenamidine, and buprofezin, fungicides, nematicides, herbicides, insect growth disruptors, and plant growth regulators. , IIa, and other agricultural chemicals, a multipurpose composition with excellent effects can be obtained, labor savings, and synergistic effects between the drugs can be fully expected.
本発明農園芸用土壌処理殺虫剤は、サツマイモ。The agricultural and horticultural soil treatment insecticide of the present invention is for sweet potatoes.
サトイモ、トマト、ナス、ピーマン、大根9人参。Taro, tomato, eggplant, green pepper, radish, 9 carrots.
ゴボウ、キャベツ、イチゴ、スイカ、カポチャ、メロン
、トウモルコシ、ジャガイモなど野菜類を加害するコガ
ネムシ類(ドウガネブイブイ、ヒメコガネ、アカビロー
ドコガネ、クロコガネなど)、ネキリムシ類(カブラヤ
ガ、タマナヤガなど)、ヨトウムシ類(ハスモンヨトウ
、ヨトウガなど)、ウリハムシ、キスジノミハムシ、タ
ネバエ、タマネギバエ。Scarab beetles that damage vegetables such as burdock, cabbage, strawberries, watermelons, kapocha, melons, corn, and potatoes (Dougan buibii, Hymeko beetles, Akabirod beetles, Black beetles, etc.), Helicoptera beetles (Kaburaya moth, Tamanaya moth, etc.), Army armyworms (Spodoptera spp. armyworm, etc.), cucurbit beetles, leaf beetles, seed flies, and onion flies.
ヒョウタンゾウムシ、ケフ、ネダニ、ダンゴムシ。Gourd weevils, kef, bed mites, pill bugs.
トビムシモドキ、コメツキ、コオロギ、カミキリムシな
どや、芝草地に生息するコガネムシ類、シパットガ、シ
バオサゾウムシ、チガヤシロオ力イガラムシなど、史に
は植物寄生性土壌線虫類などに対して高い殺虫効果を示
し、植え付は前、播種前の土壌混和処理あるいは生育時
の散布処理いずれにおいても高い防除効果を与えるもの
である。In history, it has shown a high insecticidal effect against plant-parasitic soil nematodes, such as springtail beetles, click woodpeckers, crickets, and longhorn beetles, as well as scarab beetles that live in turf grasslands, grasshopper moths, grass weevils, and longhorn beetles. A high control effect can be achieved either by mixing the soil before planting, or by spraying during growth.
また、本発明土壌処理剤は、従来の有機リン系土壌処理
殺虫剤や殺線虫剤とは作用機作が異なり、安全性や桑害
防止の点でも極めてすぐれている。Furthermore, the soil treatment agent of the present invention has a different mechanism of action from conventional organic phosphorus soil treatment insecticides and nematicides, and is extremely superior in terms of safety and prevention of mulberry damage.
次に、製剤例、試験例、実施例により本発明を更に詳細
に説明するが、本発明がこれらのみに限定されるもので
ないことはもちろんである。Next, the present invention will be explained in more detail using formulation examples, test examples, and examples, but it goes without saying that the present invention is not limited to these examples.
製剤例1 粒剤
化合物A3部、5−4216部9合成含水酸化珪素1部
、リグニンスルホン酸カルシウム2部。Formulation Example 1 Granule Compound A 3 parts, 5-4216 parts 9 synthetic hydrous silicon oxide 1 part, calcium ligninsulfonate 2 parts.
ベントナイト30部およびカオリンクレー58部をよく
粉砕混合し、水を加えてよく練り合せた後造粒乾燥して
粒剤を得る。30 parts of bentonite and 58 parts of kaolin clay are thoroughly ground and mixed, water is added and the mixture is thoroughly kneaded, followed by granulation and drying to obtain granules.
11!!+’剤例2 粉剤
化合物AO15部、S−4212,0部、安定剤スミラ
イザーBF−101(住友化学、商品名)0.05部を
8石ハイシー/L/5A3−296(日本石油、商品名
)1.0部に溶かし、これを炭酸カルシウム10部及び
カープレックス2.0部に吸着させた粉体と、トリレス
A(三共、商品名)0.5部及びDLクレー83.95
部をよく混合した後、ハンマーミルで混合粉砕してD
T、粉剤を得る。11! ! +' Agent Example 2 15 parts of powder compound AO, 0 part of S-4212, and 0.05 part of stabilizer Sumilizer BF-101 (Sumitomo Chemical, trade name) were mixed with 8 stones HiC/L/5A3-296 (Nippon Oil Co., Ltd., trade name). ) and adsorbed on 10 parts of calcium carbonate and 2.0 parts of Carplex, 0.5 part of Toriless A (Sankyo, trade name) and 83.95 parts of DL clay.
After thoroughly mixing the parts, mix and crush with a hammer mill to obtain D.
T. Obtain powder.
製剤例3 乳剤
化合物A5部、5=421 10部にソルボ−ρ5M−
200(東邦化学、商品名)5部、キシレン20部、白
灯油60部を加えこれらをよくかく拌混合溶解して乳剤
を得る。Formulation Example 3 Emulsion Compound A 5 parts, 5=421 10 parts Sorbo-ρ5M-
200 (Toho Chemical, trade name), 20 parts of xylene, and 60 parts of white kerosene were added and mixed and dissolved by stirring well to obtain an emulsion.
試験例1
製剤例3に準じて調製した下記処方乳剤の所定希釈液2
0t/を、土壌中有効成分濃度がQ、5ppmになるよ
う2種類の土壌(N3meeh)500gに混和し、こ
の土壌を直径3.53.厚さ0.50のニンジン5枚と
ともに1百径15備、高さ10備のポリエチレンカップ
に入れた。1日後及び2週間経過後、ドウガネプイプイ
(Anomalacuprθa)3令幼虫10頭放飼し
、放飼3日後の生死数を調査してその死生率を求めたと
ころ次の如くであった。Test Example 1 Specified dilution 2 of the following prescription emulsion prepared according to Formulation Example 3
0t/ is mixed with 500g of two types of soil (N3meeh) so that the active ingredient concentration in the soil is Q, 5ppm, and this soil is made into a diameter of 3.53mm. It was placed in a polyethylene cup with a diameter of 100 mm and a height of 10 mm along with 5 carrots having a thickness of 0.50 mm. After 1 day and 2 weeks, 10 3rd instar larvae of Anomalacuprθa were released, and the number of live and dead larvae was investigated 3 days after release to determine the mortality rate.The results were as follows.
1)土壌Ai有機物含量の多い黒ボク土壌2)土壌B;
有機物含量の少ない砂質土壌試験の結果、化合物Aと3
−421の組み合わせが特異的に相乗効果を示し、一方
、ピベロニルブトキサイド、サイネピリン500.セサ
ミンなどの共力剤についてはほとんど効果が認められな
かった。1) Soil Ai Kuroboku soil with high organic matter content 2) Soil B;
As a result of a sandy soil test with low organic matter content, compounds A and 3
-421 combination specifically showed synergistic effects, while piveronyl butoxide, cinepirin 500. Synergists such as sesamin had little effect.
また、有効成分として化合物Aの替わりにダイアジノン
やペルメトリンを用いた場合(対照殺虫剤5〜8)、S
−421の共力効果が認められなかったが、原因として
これらの有効成分の作用機構や土壌中年安定性等が関与
しているものと推察される。In addition, when diazinon or permethrin was used instead of compound A as an active ingredient (control insecticides 5 to 8), S
Although no synergistic effect of -421 was observed, it is presumed that the mechanism of action of these active ingredients and mid-life stability of the soil are involved.
供試土壌の土性について検討すると、一般に有機物含量
の少ない砂質土壌の方が殺虫力がすぐれ、黒ボク土壌で
は、効果が不安定化する傾向があったが、化合物Aと8
−421を組み合わせた本発明組成物のみ、土壌の土性
にかかわらず高い死生率を示した。When considering the soil properties of the test soils, it was found that sandy soils with low organic matter content generally had better insecticidal power, and in black soil, the effectiveness tended to be unstable, but Compounds A and 8
Only the composition of the present invention combined with -421 showed a high mortality rate regardless of the soil texture.
これは、5−421の殺虫効力の相乗的寄与のみならず
、S−421を加えることによフて土壌脱着性が改良さ
れ、化合物Aの土壌中有機物への吸着が軽減し不動化が
抑えられたことによるものと考えられる。This is due not only to the synergistic contribution of the insecticidal efficacy of 5-421, but also to the addition of S-421, which improves soil desorption properties, reduces the adsorption of Compound A to organic matter in the soil, and suppresses immobilization. This is thought to be due to the fact that
試験例2
試験例】に準じて下記処方乳剤を用いて土壌処理試、験
を行ったところ以下の如くであった。Test Example 2 A soil treatment test was conducted using the following formulated emulsion according to Test Example, and the results were as follows.
試験の結果、化合物AにS−421を配合することによ
って高い共力効果が認められたが、S−421の混合比
が高くなりすぎると(試料&7)、土壌脱着性の点でマ
イナスに働き、かえって効力が減少した。As a result of the test, a high synergistic effect was observed by blending S-421 with Compound A, but when the mixing ratio of S-421 was too high (Sample & 7), it had a negative effect on soil desorption. , on the contrary, the efficacy decreased.
従って相乗効果を奏する化合物Aと5−421の混合比
は、2:1〜110(好ましくは1:1〜1:5)が適
当であることが明らかとなった。Therefore, it has been revealed that the appropriate mixing ratio of Compound A and 5-421, which exhibits a synergistic effect, is 2:1 to 110 (preferably 1:1 to 1:5).
実施例1
化合物AI部、5−4213部、ダイアジノン2部9合
成含水酸化珪素1部、リグニンスルホン酸カルシウム2
部、ベントナイト30部およびカオリンクレー61部を
よく粉砕混合し水を加えてよく練り合せた後造粒乾燥し
て粒剤を得た。Example 1 Part of compound AI, 5-4213 parts, 2 parts of diazinon, 9 parts of synthetic hydrous silicon oxide, 2 parts of calcium lignin sulfonate
1 part, 30 parts of bentonite, and 61 parts of kaolin clay were thoroughly ground and mixed, water was added, the mixture was thoroughly kneaded, and the mixture was granulated and dried to obtain granules.
さつまいも挿苗前に、畦内の元肥位置に10aあた。9
5に9散布し土壌とよく混和した。Before cutting sweet potato seedlings, apply 10a of fertilizer to the base of the furrow. 9
It was sprayed 5 to 9 times and mixed well with the soil.
畦立て後ビニールでマルチを張り、栽培したところドウ
ガネプイブイ、ヒメコガネなどのコガネムシ類や、ケラ
、ネキリムシなど土壌害虫の加害を防除することができ
、薬害は全く認められなかった。After the ridges were raised, the cultivation was covered with vinyl mulch, and it was possible to control the damage caused by scarab beetles, such as the Japanese brown beetles and the Japanese red beetles, as well as soil pests, such as the mole crickets and the white beetles, and no chemical damage was observed.
実施例2
化合物A0.5部、5−421 2.0部を8石ハイシ
ー/l/S A S−296(日本石油、商品名)1.
0部に溶かし、カープレックス2.0部、トリプロピレ
ンゲフィコ−/l’1.o部及びDLクレー93.5部
を加えてよく混合した後、ハンマーミρで混合粉砕して
DL扮剤を得た。Example 2 0.5 parts of Compound A and 2.0 parts of 5-421 were mixed with 8 stone HiC/l/SA S-296 (Nippon Oil Co., Ltd., trade name) 1.
0 parts of Carplex, 2.0 parts of Tripropylene Gefico/l'1. After adding o parts and 93.5 parts of DL clay and mixing well, the mixture was mixed and pulverized using a hammer mill ρ to obtain a DL dressing.
ダイズ、インゲンの播種時に、播穴に10aあた、93
kg施用し土壌とよく混和処理を行ったところタネバエ
類の被害をほとんど受けなかった。When sowing soybeans and green beans, 10a per hole in the seeding hole, 93
When I applied it and mixed it well with the soil, there was almost no damage from seed flies.
実施例3
化合物A10部、5−42110部、ソ/レポール24
95(東邦化学、商品名)2部、サンエキスP−201
(山陽国策パルプ、商品名)2部、ホワイトカーボン1
5部及びカオリンクレー61部を混合機中で均一に混合
し有効成分が10%の水和剤を得た。Example 3 Compound A 10 parts, 5-42110 parts, So/Repol 24
95 (Toho Chemical, trade name) 2 parts, Sunextract P-201
(Sanyo Kokusaku Pulp, product name) 2 parts, white carbon 1
5 parts of kaolin clay and 61 parts of kaolin clay were uniformly mixed in a mixer to obtain a wettable powder containing 10% of the active ingredient.
イネオサゾウムシの被害が発生した芝生にこの水利剤の
2000倍水希釈液を適用した時、加害の進行を完全に
抑えることができ、芝生に対する薬害や付近の水系魚介
類に対する毒性の問題は全くなかった。When a 2,000-fold dilution of this irrigation agent is applied to lawns infested with rice weevil, the progress of the damage can be completely suppressed, and there are no chemical damage to the lawn or toxicity to nearby aquatic fish and shellfish. There wasn't.
本発明の農園芸用土壌処理殺虫剤は、土壌中の安定性に
すぐれ、更に施用土壌の土性や気象条件に左右されるこ
となく安定して高い防除効果を与え、かつ安全性や薬害
防止の点ですぐれていることから極めて実用性の高い製
剤である。The agricultural and horticultural soil treatment insecticide of the present invention has excellent stability in soil, provides stable and high pest control effects regardless of the soil texture and weather conditions of the applied soil, and is safe and prevents chemical damage. It is an extremely practical formulation because of its excellent properties.
第1図は試験例2の化合物A 、S−421各成分の濃
度と、供試土壌Aにおける死去率との関係を示したもの
であり、点線より上部は共力作用領域を示す。
特許出願人 大11木除蟲菊株式会社
代表取締役 上 山 英 介FIG. 1 shows the relationship between the concentration of each component of Compound A and S-421 in Test Example 2 and the mortality rate in test soil A, and the area above the dotted line shows the synergistic action area. Patent applicant: Eisuke Kamiyama, Representative Director of Dai 11 Kijo Mugiku Co., Ltd.
Claims (1)
ノキシ−4−フルオロフェニル)プロピル}シランとオ
クタクロロジプロピルエーテルを含有することを特徴と
する農園芸用土壌処理殺虫剤An agricultural and horticultural soil treatment insecticide characterized by containing dimethyl-(4-ethoxyphenyl) {3-(3-phenoxy-4-fluorophenyl)propyl}silane and octachlorodipropyl ether
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP63263517A JP2798939B2 (en) | 1988-10-19 | 1988-10-19 | Agricultural and horticultural soil treatment insecticides |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP63263517A JP2798939B2 (en) | 1988-10-19 | 1988-10-19 | Agricultural and horticultural soil treatment insecticides |
Publications (2)
Publication Number | Publication Date |
---|---|
JPH02111706A true JPH02111706A (en) | 1990-04-24 |
JP2798939B2 JP2798939B2 (en) | 1998-09-17 |
Family
ID=17390637
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
JP63263517A Expired - Fee Related JP2798939B2 (en) | 1988-10-19 | 1988-10-19 | Agricultural and horticultural soil treatment insecticides |
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Citations (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPS6187687A (en) * | 1984-10-05 | 1986-05-06 | Yoshio Katsuta | Insecticide and acaricide containing organosilicon aromatic alkane derivative and their production |
JPS63170386A (en) * | 1987-12-19 | 1988-07-14 | Dainippon Jiyochiyuugiku Kk | Organosilicon based aromatic alkane derivative and production thereof |
-
1988
- 1988-10-19 JP JP63263517A patent/JP2798939B2/en not_active Expired - Fee Related
Patent Citations (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPS6187687A (en) * | 1984-10-05 | 1986-05-06 | Yoshio Katsuta | Insecticide and acaricide containing organosilicon aromatic alkane derivative and their production |
JPS63170386A (en) * | 1987-12-19 | 1988-07-14 | Dainippon Jiyochiyuugiku Kk | Organosilicon based aromatic alkane derivative and production thereof |
Also Published As
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JP2798939B2 (en) | 1998-09-17 |
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