JPH09291002A - Controlling agent composition for insect pest of citrus fruits and controlling method - Google Patents

Controlling agent composition for insect pest of citrus fruits and controlling method

Info

Publication number
JPH09291002A
JPH09291002A JP35443796A JP35443796A JPH09291002A JP H09291002 A JPH09291002 A JP H09291002A JP 35443796 A JP35443796 A JP 35443796A JP 35443796 A JP35443796 A JP 35443796A JP H09291002 A JPH09291002 A JP H09291002A
Authority
JP
Japan
Prior art keywords
group
citrus
composition
controlling
chloro
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
Application number
JP35443796A
Other languages
Japanese (ja)
Other versions
JP3965456B2 (en
Inventor
Shinji Mizobe
信二 溝部
Akiyoshi Miyata
明義 宮田
Kenji Saito
健志 斉藤
Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)
YAMAGUCHI PREF GOV
Nippon Soda Co Ltd
Original Assignee
YAMAGUCHI PREF GOV
Nippon Soda Co Ltd
Priority date (The priority date 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 date listed.)
Filing date
Publication date
Application filed by YAMAGUCHI PREF GOV, Nippon Soda Co Ltd filed Critical YAMAGUCHI PREF GOV
Priority to JP35443796A priority Critical patent/JP3965456B2/en
Publication of JPH09291002A publication Critical patent/JPH09291002A/en
Application granted granted Critical
Publication of JP3965456B2 publication Critical patent/JP3965456B2/en
Anticipated expiration legal-status Critical
Expired - Lifetime legal-status Critical Current

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  • Cultivation Of Plants (AREA)
  • Agricultural Chemicals And Associated Chemicals (AREA)
  • Compositions Of Macromolecular Compounds (AREA)

Abstract

PROBLEM TO BE SOLVED: To obtain the subject new agrochemical capable of controlling damages due to insect pests damaging new buds of plants, especially citrus fruits, etc. SOLUTION: This controlling agent composition for insect pests of citrus fruits comprises (A) 0.1-10wt.% systemic insecticide represented by formula I [R is H, formyl, etc.; A is H, a 1-4C alkyl or formula II (R<1> is H or a 1-4C alkyl) bonded to B; B is a 1-4C alkyl, a group represented by SR<2> (R<2> is a 1-4C alkyl) or formula III (R<3> and R<4> are each H, methyl, etc.), methyl group bonded to A or a group represented by formula IV (R<5> is H or a 1-4C alkyl); Y is N or CR<6> (R<6> is H or a 1-4C alkyl); X is nitro or cyano], e.g. N-cyano-N-(2- chloro-5-pyridylmethyl)-N'-methylacetamide and (B) a vinyl acetate-based polymer such as a vinyl acetate resin. The composition is applied to a pruned cut surface or injected into a grafting treated part of a plant.

Description

【発明の詳細な説明】Detailed Description of the Invention

【0001】[0001]

【発明の属する技術分野】本発明は、農園芸作物、特に
柑橘類をせん定した際の切断面及び接木処理部の新芽を
加害する植物害虫を防除する新しい薬剤および防除方法
に関する。
BACKGROUND OF THE INVENTION 1. Field of the Invention The present invention relates to a new chemical agent and a method for controlling a plant pest which damages agricultural and horticultural crops, especially cut surfaces of pesticides of citrus fruits and sprouts on the grafted portion.

【0002】[0002]

【従来の技術】特開平4−154741号、特開昭61
−106854号、特開平3−218370号や特開平
2−171号等に記載される化合物は、従前の有機リン
系並びにカーバメート系殺虫剤に比し、極めて低薬量で
的確に作用し浸透性を有するクロロニコチニル系殺虫性
化合物である。また、本発明に近い公知技術として、特
開平7−291802号に記載のペースト状農薬製剤が
知られており、クロロニコチニル系殺虫剤にアジュバン
トを添加したペースト状農薬製剤を、植物体表面又は植
物表面の切り口部に塗布等する技術が開示されている。
しかし、この公報に記載されているアジュバントはソル
ビタンモノラウレート、ポリオキシエチレンソルビタン
モノラウレート、オレイン酸ポリエチレングリコールエ
ステルなどであり、酢酸ビニル系高分子を含有させる点
については何らの記載はない。さらに、酢酸ビニル系高
分子を含有した農園芸用殺菌剤組成物として、日本曹達
(株)製のトップジンMペースト剤が知られているが、
酢酸ビニル系高分子を含有する植物害虫の防除剤組成物
は知られていない。
2. Description of the Related Art JP-A-4-1547471 and JP-A-61
The compounds described in JP-A-106854, JP-A-3-218370, JP-A-2-171, and the like act properly with extremely low doses compared to the conventional organic phosphorus-based and carbamate-based insecticides, and have permeability. Is a chloronicotinyl-based insecticidal compound having Further, as a known technique close to the present invention, a pasty agricultural chemical preparation described in JP-A-7-291802 is known, and a pasty agricultural chemical preparation obtained by adding an adjuvant to a chloronicotinyl insecticide is used on the plant surface or A technique of applying it to a cut surface portion of a plant surface is disclosed.
However, the adjuvants described in this publication are sorbitan monolaurate, polyoxyethylene sorbitan monolaurate, polyethylene glycol oleate, etc., and there is no description about the inclusion of vinyl acetate polymer. Further, as a fungicide composition for agricultural and horticultural use containing a vinyl acetate polymer, Topzin M paste agent manufactured by Nippon Soda Co., Ltd. is known.
No plant pest control composition containing a vinyl acetate polymer is known.

【0003】[0003]

【発明が解決しようとする課題】従来、ミカンをはじめ
とする柑橘類、特に青島温州や大津4号等の高糖度系品
種は、大果になりやすいうえ強い隔年結果を起こす性質
があり、そのため、若齢期間には商品性の高いL、M級
の果実を安定して生産することは困難であった。その対
策として、枝の伸長期間(8月上旬〜8月下旬)に夏季
せん定により、優良な夏枝を確保する方法がとられてい
るが、その際のせん定切断面から水分が過剰に失われる
ことや植物病原菌の感染によって枝の一部が枯れ、植物
にダメージを与えることがあるが、何ら効果的な対策が
実施されていない。そのうえ、発生する新梢には、ミカ
ンハモグリガ、アブラムシ類、ハマキムシ類等の害虫が
多発し、健全な枝の確保が困難となっている。
Conventionally, citrus fruits such as mandarin orange, especially high sugar content varieties such as Qingdao Wenzhou and Otsu No. 4 are prone to large fruits and have the property of causing strong biennial results. During the young period, it was difficult to stably produce L- and M-class fruits with high commercial value. As a countermeasure for this, a method of securing good summer branches by summer pruning during the branch extension period (early August to late August) is used, but excessive loss of water from the pruning cut surface at that time. Although some of the branches may die due to infection with phytopathogenic bacteria and damage plants, no effective measures have been taken. Moreover, pests such as citrus leafminer, aphids, and leaf beetles frequently occur in the new shoots, which makes it difficult to secure healthy branches.

【0004】一方、果樹等の永年性作物の優良品種・系
統の増殖は、接木によって行われている。また、農家が
既存品種を変更する場合は、多数の穂木を成木(中間台
木)に接木して、短期間で収穫可能とする高接一挙更新
が一般的である。いずれの場合も、芽の伸長する時期
は、前記の如き害虫の発生時期と重複するため、害虫防
除のために、定期的な殺虫剤の散布を実施している。し
かしながら、高接更新では、生育差の大きい芽が長期間
にわたって混在するため、防除効果も不安定で、優良な
枝の確保が困難である。そのため、それを防除する方法
として、夏枝の伸長期間(8月上旬〜下旬)に2〜3回
の殺虫剤の定期的な散布が繰り返されているが、夏季高
温時でもあり、労力面で農家に負担となっていた。本発
明は、かかる問題点を解決する樹木の害虫、特に、柑橘
類などの新芽を加害する害虫の防除剤組成物および該組
成物を用いた植物害虫の防除方法を提供することを目的
とする。
On the other hand, the propagation of excellent varieties and lines of perennial crops such as fruit trees is carried out by grafting. In addition, when farmers change existing varieties, it is common to replant a large number of spikes onto a mature tree (intermediate rootstock) to enable harvesting in a short period of time. In either case, the time of bud elongation overlaps with the time of occurrence of the pests as described above, and therefore pesticides are regularly sprayed to control the pests. However, in high contact renewal, buds with a large growth difference are mixed for a long period of time, so that the control effect is unstable and it is difficult to secure good branches. Therefore, as a method of controlling it, the insecticide is regularly sprayed 2-3 times during the extension period of the summer branches (early to late August), but it is also at high temperature in summer and the farmer is labor-intensive. Was a burden to An object of the present invention is to provide a pest control composition for tree pests, in particular, a pest control agent for damaging shoots such as citrus fruits, and a method for controlling plant pests using the composition, which solves the above problems.

【0005】[0005]

【課題を解決するための手段】本発明者らは鋭意研究の
結果、浸透性殺虫剤および酢酸ビニル系高分子を含有す
る組成物を柑橘類のせん定の際に生じる切断面に塗布す
ることにより、また、柑橘類などの植物の接木部分に該
組成物を注入することにより、新芽を加害する害虫等に
よる被害を極めて効果的に防除できることを見い出し、
本発明を完成した。
Means for Solving the Problems As a result of intensive studies by the present inventors, by applying a composition containing a penetrating insecticide and a vinyl acetate polymer to a cut surface produced during pruning of citrus fruits, Further, by injecting the composition into the grafted portion of plants such as citrus fruits, it was found that damage by pests etc. that harm the shoots can be controlled very effectively,
The present invention has been completed.

【0006】[0006]

【発明の実施の形態】以下、本発明を詳細に説明する。
本発明は、浸透性殺虫剤および酢酸ビニル系接着剤や酢
酸ビニル樹脂などの酢酸ビニル系高分子を含有すること
を特徴とする柑橘類植物のせん定をした切断面に塗布す
る柑橘類害虫の防除剤組成物、あるいは、植物の接木部
分に注入する柑橘類害虫などの植物害虫の防除剤組成
物、および該組成物を用いた植物害虫の防除方法であ
る。
BEST MODE FOR CARRYING OUT THE INVENTION The present invention will be described in detail below.
The present invention is a citrus pest control agent composition to be applied to a pruned cut surface of a citrus plant characterized by containing a vinyl acetate polymer such as a penetrating insecticide and a vinyl acetate adhesive or a vinyl acetate resin. The present invention relates to a composition for controlling plant pests such as citrus pests, which is injected into a plant or a grafted part of a plant, and a method for controlling plant pests using the composition.

【0007】本発明に使用される浸透性殺虫剤は、浸透
移行性を有するものであれば限定されないが、特に、下
記式〔I〕
The osmotic insecticide used in the present invention is not particularly limited as long as it has an osmotic migration property. In particular, the following formula [I]

【0008】[0008]

【化5】 Embedded image

【0009】〔式中、Rは、水素原子、ホルミル基、ア
セチル基、C1-4 アルキル基、2−クロロ−5−ピリジ
ルメチル基又は2−クロロ−5−チアゾリルメチル基を
示し、Aは、水素原子、メチル、エチル、プロピル、イ
ソプロピル、ブチル、t−ブチル基等の直鎖若しくは分
岐のC1-4 アルキル基、Bと結合するエチレン基、Bと
結合するトリメチレン基又はBと結合する化2、
[In the formula, R represents a hydrogen atom, a formyl group, an acetyl group, a C 1-4 alkyl group, a 2-chloro-5-pyridylmethyl group or a 2-chloro-5-thiazolylmethyl group, and A is Hydrogen atom, linear or branched C 1-4 alkyl group such as methyl, ethyl, propyl, isopropyl, butyl, t-butyl group, ethylene group bonded to B, trimethylene group bonded to B or compound bonded to B 2,

【0010】[0010]

【化6】 [Chemical 6]

【0011】で表される基を表す(R1 は、水素原子又
はメチル、エチル、プロピル、イソプロピル、ブチル、
t−ブチル基等の直鎖若しくは分岐のC1-4 アルキル基
を表す。)。Bは、C1-4 アルキル基、SR2 (R2
は、メチル、エチル、プロピル、イソプロピル、ブチ
ル、t−ブチル基等の直鎖若しくは分岐のC1-4 アルキ
ル基を表す。)、化3、
Represents a group represented by (R 1 is a hydrogen atom or methyl, ethyl, propyl, isopropyl, butyl,
It represents a linear or branched C 1-4 alkyl group such as t-butyl group. ). B is a C 1-4 alkyl group, SR 2 (R 2
Represents a linear or branched C 1-4 alkyl group such as methyl, ethyl, propyl, isopropyl, butyl, t-butyl group. ), Chemical formula 3,

【0012】[0012]

【化7】 Embedded image

【0013】(ここで、R3 、R4 は、水素原子、メチ
ル基又はエチル基を表す。)で表される基、Aと結合す
る−S−、Aと結合するメチレン基又はAと結合する化
4、
(Wherein R 3 and R 4 represent a hydrogen atom, a methyl group or an ethyl group), —S— bonded to A, a methylene group bonded to A, or bonded to A. Conversion 4,

【0014】[0014]

【化8】 Embedded image

【0015】(ここで、R5 は水素原子又はメチル、エ
チル基等のC1-4 アルキル基を表す。)で表される基を
表す。Yは、N又はCR6 を示し(R6 は水素原子又は
1-4アルキル基を表す。)、また、Xはニトロ基又は
シアノ基を表す。〕で表される化合物の使用が好まし
い。
(Wherein R 5 represents a hydrogen atom or a C 1-4 alkyl group such as a methyl or ethyl group). Y represents N or CR 6 (R 6 represents a hydrogen atom or a C 1-4 alkyl group), and X represents a nitro group or a cyano group. ] The use of a compound represented by

【0016】より好ましくは、本発明に使用される浸透
性殺虫剤として以下の化合物を例示することができる。 (1)N−シアノ−N−(2−クロロ−5−ピリジルメ
チル)−N’−メチルアセトアミジン (2)1−〔N−(6−クロロ−3−ピリジルメチル)
−N−エチルアミノ〕−1−メチルアミノ−2−ニトロ
エチレン、(3)1−(2−クロロ−5−ピリジルメチ
ル)−5−メチル−2−ニトロイミノ−ヘキサヒドロ−
1,3,5−トリアジン、(4)1−(2−クロロ−5
−チアゾリルメチル)−3,5−ジメチル−2−ニトロ
イミノ−ヘキサヒドロ−1,3,5−トリアジン、
(5)1−(2−クロロ−5−ピリジルメチル)−3,
5−ジメチル−2−ニトロイミノ−ヘキサヒドロ−1,
3,5−トリアジン、(6)1−(2−クロロ−5−ピ
リジルメチル)−2−ニトロメチレン−イミダゾリジ
ン、(7)1−〔N−(2−クロロ−5−チアゾリルメ
チル)−N−エチルアミノ〕−1−メチルアミノ−2−
ニトロエチレン (8)3−(2−クロロ−5−ピリジルメチル)−2−
ニトロメチレン−チアゾリジン、(9)1−(2−クロ
ロ−5−ピリジルメチル)−2−(1−ニトロ−2−ア
リルチオエチリデン)イミダゾリジン、(10)1−
(2−クロロ−5−ピリジルメチル)−2−(1−ニト
ロ−2−エチルチオエチリデン)イミダゾリジン、(1
1)1−(2−クロロ−5−ピリジルメチル)−2−
(1−ニトロ−2−β−メチルアリルチオエチリデン)
イミダゾリジン (12)メチル−〔3−(2−クロロ−5−ピリジルメ
チル)−1−メチル−2−ニトロ〕グアニジノホルマー
ト、(13)1−(2−クロロ−5−ピリジルメチルア
ミノ)−1−メチルチオ−2−ニトロエチレン、(1
4)1−(2−クロロ−5−ピリジルメチルアミノ)−
1−メチルアミノ─2−ニトロエチレン、(15)1−
(2−クロロ−5−ピリジルメチル)−3−ニトロ−2
−メチルイソチオウレア、(16)1−(2−クロロ−
5−ピリジルメチル)−1−メチル−2−ニトログアニ
ジン、(17)1−(2−クロロ−5−ピリジルメチル
アミノ)−1−ジメチルアミノ−2−ニトロエチレン、
(18)1−〔N−(2−クロロ−5−ピリジルメチ
ル)−N−メチルアミノ〕−1−メチルアミノ−2−ニ
トロエチレン、(19)1−〔N−(2−クロロ−5−
ピリジルメチル)−N−メチルアミノ〕−1−ジメチル
アミノ−2−ニトロエチレン、(20)3−(2−クロ
ロ−5−ピリジルメチル)−1,1−ジメチル−2−ニト
ログアニジン、(21)1−(2−クロロ−5−ピリジ
ルメチルアミノ)−1−エチルアミノ−2-ニトロエチレ
ン、(22)1−アミノ−1−〔N−(2−クロロ−5
−ピリジルメチル)−N−メチルアミノ〕−2−ニトロ
エチレン、(23)3−(2−クロロ−5−ピリジルメ
チル)−1,3−ジメチル−2−ニトログアニジン、
(24)3−(2−クロロ−5−ピリジルメチル)−
1,1,3−トリメチル−2−ニトログアニジン、(2
5)1−アミノ−1−〔N−(2−クロロ−5−ピリジ
ルメチル)−N−エチルアミノ〕−2−ニトロエチレ
ン、(26)1−〔N−(2−クロロ−5−ピリジルメ
チル)−N−エチルアミノ〕−N−n−プロピルアミ
ノ〕−1−メチルアミノ−2−ニトロエチレン、(2
7)1−〔N−(2−クロロ−5−ピリジルメチル)−
N−エチルアミノ〕−1−エチルアミノ−2−ニトロエ
チレン、(28)3−(2−クロロ−5−ピリジルメチ
ル)−3−エチル−1−メチル−2-ニトログアニジン、
(29)3−(2−クロロ−5−チアゾリルメチル)−
1−メチル−2−ニトログアニジン、(30)1−(6
−クロロ−3−ピリジルメチル)−N−ニトロイミダゾ
リン−2−イリデンアミン等。
More preferably, the following compounds can be exemplified as the penetrating insecticide used in the present invention. (1) N-cyano-N- (2-chloro-5-pyridylmethyl) -N'-methylacetamidine (2) 1- [N- (6-chloro-3-pyridylmethyl)
-N-ethylamino] -1-methylamino-2-nitroethylene, (3) 1- (2-chloro-5-pyridylmethyl) -5-methyl-2-nitroimino-hexahydro-
1,3,5-triazine, (4) 1- (2-chloro-5
-Thiazolylmethyl) -3,5-dimethyl-2-nitroimino-hexahydro-1,3,5-triazine,
(5) 1- (2-chloro-5-pyridylmethyl) -3,
5-dimethyl-2-nitroimino-hexahydro-1,
3,5-triazine, (6) 1- (2-chloro-5-pyridylmethyl) -2-nitromethylene-imidazolidine, (7) 1- [N- (2-chloro-5-thiazolylmethyl) -N- Ethylamino] -1-methylamino-2-
Nitroethylene (8) 3- (2-chloro-5-pyridylmethyl) -2-
Nitromethylene-thiazolidine, (9) 1- (2-chloro-5-pyridylmethyl) -2- (1-nitro-2-allylthioethylidene) imidazolidine, (10) 1-
(2-chloro-5-pyridylmethyl) -2- (1-nitro-2-ethylthioethylidene) imidazolidine, (1
1) 1- (2-chloro-5-pyridylmethyl) -2-
(1-nitro-2-β-methylallylthioethylidene)
Imidazolidine (12) Methyl- [3- (2-chloro-5-pyridylmethyl) -1-methyl-2-nitro] guanidinoformate, (13) 1- (2-chloro-5-pyridylmethylamino)- 1-methylthio-2-nitroethylene, (1
4) 1- (2-chloro-5-pyridylmethylamino)-
1-methylamino-2-nitroethylene, (15) 1-
(2-chloro-5-pyridylmethyl) -3-nitro-2
-Methylisothiourea, (16) 1- (2-chloro-
5-pyridylmethyl) -1-methyl-2-nitroguanidine, (17) 1- (2-chloro-5-pyridylmethylamino) -1-dimethylamino-2-nitroethylene,
(18) 1- [N- (2-chloro-5-pyridylmethyl) -N-methylamino] -1-methylamino-2-nitroethylene, (19) 1- [N- (2-chloro-5-
Pyridylmethyl) -N-methylamino] -1-dimethylamino-2-nitroethylene, (20) 3- (2-chloro-5-pyridylmethyl) -1,1-dimethyl-2-nitroguanidine, (21) 1- (2-chloro-5-pyridylmethylamino) -1-ethylamino-2-nitroethylene, (22) 1-amino-1- [N- (2-chloro-5
-Pyridylmethyl) -N-methylamino] -2-nitroethylene, (23) 3- (2-chloro-5-pyridylmethyl) -1,3-dimethyl-2-nitroguanidine,
(24) 3- (2-chloro-5-pyridylmethyl)-
1,1,3-trimethyl-2-nitroguanidine, (2
5) 1-amino-1- [N- (2-chloro-5-pyridylmethyl) -N-ethylamino] -2-nitroethylene, (26) 1- [N- (2-chloro-5-pyridylmethyl) ) -N-Ethylamino] -Nn-propylamino] -1-methylamino-2-nitroethylene, (2
7) 1- [N- (2-chloro-5-pyridylmethyl)-
N-ethylamino] -1-ethylamino-2-nitroethylene, (28) 3- (2-chloro-5-pyridylmethyl) -3-ethyl-1-methyl-2-nitroguanidine,
(29) 3- (2-chloro-5-thiazolylmethyl)-
1-methyl-2-nitroguanidine, (30) 1- (6
-Chloro-3-pyridylmethyl) -N-nitroimidazoline-2-ylideneamine and the like.

【0017】本発明において、組成物中の浸透性殺虫剤
の含有量は、0.1〜10%が好ましい。組成物中に添
加される接着剤としては、必要とされる機能として、
(i)有効成分が容易に植物体に移行しうるものである
こと、(ii)表面が乾燥することによって作業着に再付
着しないものであること、(iii)降水や夜霧によって再
び柔らかくなり、有効成分が再び植物体に移行するもの
であること、及び(iv)植物の生育に悪影響を与えない
ものであることを備えたものであれば、特に制限はな
い。例えば、酢酸ビニル系接着剤(木工用ボンド)、酢
酸ビニル樹脂などの酢酸ビニル系高分子等を挙げること
ができる。
In the present invention, the content of the penetrating insecticide in the composition is preferably 0.1 to 10%. As an adhesive added to the composition, as a required function,
(I) that the active ingredient can be easily transferred to the plant, (ii) that the surface does not reattach to work clothes due to drying, (iii) becomes soft again due to precipitation or night fog, There is no particular limitation as long as the active ingredient is transferred to the plant again and (iv) it does not adversely affect the growth of the plant. For example, vinyl acetate-based adhesives (bonds for woodworking), vinyl acetate-based polymers such as vinyl acetate resins, and the like can be mentioned.

【0018】また、本発明組成物に殺菌剤を含有させる
ことも可能である。使用できる殺菌剤としては、例え
ば、塗布殺菌剤の形態として、チオファネートメチル含
有殺菌塗布剤(商品名:トップジンMペースト:日本曹
達(株))、有機銅系殺菌塗布剤(商品名:バッチレー
ト:トモノアグリカ(株))、ポリオキシン含有殺菌塗
布剤(商品名:カケンゲル:科研製薬(株))、イミノ
クタジン酸塩含有殺菌塗布剤(商品名:ベフラン塗布
剤:サンケイ化学(株)etc.)などを挙げることができ
る。かかる殺菌剤の製剤中含有量は、通常、0.1〜1
0%程度である。かかる殺菌剤を含有させた場合には、
柑橘類に発生する植物害虫のみならず、植物病害をも同
時に防除できるので特に好ましい。
It is also possible to add a bactericide to the composition of the present invention. Examples of germicides that can be used include, in the form of coating germicides, thiophanatemethyl-containing germicides (trade name: Topzin M Paste: Nippon Soda Co., Ltd.), organic copper germicides (trade name: batch rate: Tomonoagrica). Co., Ltd.), polyoxin-containing germicidal coating agent (trade name: Kakengel: Kaken Pharmaceutical Co., Ltd.), iminoctazinate-containing germicidal coating agent (trade name: Befran coating agent: Sankei Chemical Co., Ltd., etc.) You can The content of the bactericide in the preparation is usually 0.1 to 1
It is about 0%. When containing such a bactericide,
It is particularly preferable because not only plant pests that occur in citrus fruits but also plant diseases can be controlled at the same time.

【0019】また、本発明の薬剤組成物中には、作業の
効率化、ゆ合促進、新梢の発生促進のため、必要に応じ
て色素、植物ホルモン剤等の他の添加剤を添加すること
ができる。
In addition, in the pharmaceutical composition of the present invention, other additives such as pigments and phytohormonal agents are added, if necessary, in order to improve work efficiency, promotion of mixing, and promotion of shoot development. be able to.

【0020】本発明の組成物は、主に温州ミカンなどの
柑橘類の夏期せん定後の植物病害虫の防除のためにせん
定の切断面に塗布して使用することができる。その使用
例を図1に示す。すなわち、図1において、せん定の切
断面に本発明の薬剤を直接に塗布すると、塗布した薬
剤は浸透移行性を有するので、切断面付近の新梢に
も浸透し、害虫の被害を防除できるものである。また、
本発明の組成物は、柑橘類の接木処理時の植物病害虫の
防除のために、接木処理部に該組成物を注入して使用
することができる。その使用例を図2に示す。接木した
穂木の固定と保護のために巻いたテープ(接木テー
プ)は、新芽が伸びはじめた時期にナイフ等で切開する
処理を行っている。この切開処理時に、接木部分に薬
剤を注入すると、薬剤は穂木から発生する新梢に移行
し、害虫を防除する。なお、本発明組成物は、柑橘類の
みならず、他の果樹、バラなどの鑑賞用植物等の害虫の
防除にも使用することができるのはいうまでもない。
The composition of the present invention can be used by applying it to the cut surface of pruning for controlling the plant pests after the summer pruning of citrus fruits such as Satsuma mandarin. An example of its use is shown in FIG. That is, in FIG. 1, when the agent of the present invention is directly applied to the cut surface of pruning, the applied agent has a penetrating and migrating property, so that it penetrates into shoots near the cut surface and can prevent damage of pests. Is. Also,
The composition of the present invention can be used by injecting the composition into a grafted part for controlling plant pests during citrus grafting. An example of its use is shown in FIG. The tape (grafted tape) wrapped to fix and protect the grafted scion is cut with a knife when the shoots start to grow. When a drug is injected into the grafted portion during this incision process, the drug moves to shoots emerging from the scion and controls pests. Needless to say, the composition of the present invention can be used not only for citrus fruits but also for controlling harmful insects such as ornamental plants such as fruit trees and roses.

【0021】[0021]

【実施例】次に、実施例により本発明をさらに詳細に説
明する。 (1)薬剤の調製 浸透性殺虫剤であるクロロニコチニル系殺虫剤(アセタ
ミプリド又はイミダクロプリド)と、酢酸ビニル樹脂含
有物〔チオファネートメチル塗布剤(商品名:トップジ
ンMペースト)〕、酢酸ビニル系接着剤(商品名:木工
用ボンド)、鉱物質澱粉、界面活性剤等を以下の所定の
割合で混合し調製した。なお、アセタミプリド(日本曹
達(株)製)は原末及び市販のモスピラン水和剤(日本
曹達(株)製)を、イミダクロプリドは市販されている
アドマイヤー水和剤(日本バイエルアグロケム(株)
製)を使用し、有効成分が2%になるように混合した。
Next, the present invention will be described in more detail with reference to examples. (1) Preparation of drug A chloronicotinyl insecticide (acetamiprid or imidacloprid) which is a penetrating insecticide, a vinyl acetate resin-containing material [thiophanate methyl coating agent (trade name: Topzin M paste)], a vinyl acetate adhesive ( Trade name: bond for woodworking), mineral starch, surfactant, etc. were mixed and prepared at the following predetermined ratios. In addition, acetamiprid (manufactured by Nippon Soda Co., Ltd.) is a bulk powder and a commercially available mospiran wettable powder (manufactured by Nippon Soda Co., Ltd.), and imidacloprid is a commercially available Admeier wettable powder (Japan Bayer Agrochem Co., Ltd.).
(Manufactured by K.K.) was used and mixed so that the active ingredient was 2%.

【0022】実施例1 アセタミプリド : 2部 鉱物質微粉,界面活性剤等 :18部 木工用ボンド :80部Example 1 Acetamiprid: 2 parts Mineral fine powder, surfactant, etc .: 18 parts Woodworking bond: 80 parts

【0023】実施例2 アセタミプリド : 2部 鉱物質微粉,界面活性剤等 :18部 チオファネートメチル塗布剤 :80部Example 2 Acetamiprid: 2 parts Mineral fine powder, surfactant, etc .: 18 parts Thiophanatomethyl coating agent: 80 parts

【0024】実施例3 イミダクロプリド : 2部 鉱物質微粉,界面活性剤等 :18部 木工用ボンド :80部Example 3 Imidacloprid: 2 parts Mineral fine powder, surfactant, etc .: 18 parts Woodworking bond: 80 parts

【0025】実施例4 イミダクロプリド : 2部 鉱物質微粉,界面活性剤等 :18部 チオファネートメチル塗布剤 :80部Example 4 Imidacloprid: 2 parts Mineral fine powder, surfactant, etc .: 18 parts Thiophanatomethyl coating agent: 80 parts

【0026】実施例5 アセタミプリド : 2部 鉱物質微粉,界面活性剤等 :18部 木工用ボンド :80部Example 5 Acetamiprid: 2 parts Fine mineral powder, surfactant, etc .: 18 parts Bond for woodworking: 80 parts

【0027】(2)薬剤処理の方法 試験例1 図1に示すように、青島温州(高糖度系温州ミカン品種
の一つ)の直径約1cmの枝を切除し、切断面に調製し
た薬剤を塗布した。処理35日後に切断面からの距離及
び展開葉におけるミカンハモリガ被害を調査した。調査
結果を表1に示す。表1に示すように、浸透性殺虫剤で
あるアセタミプリド剤及びイミダクロプリド剤は、切断
面周辺部の新梢に発生するミカンハモグリガの被害を防
止した。
(2) Method of Drug Treatment Test Example 1 As shown in FIG. 1, a branch of Qingdao Wenzhou (one of the high sugar content Wenzhou mandarin varieties) with a diameter of about 1 cm was cut off, and a drug prepared on the cut surface was prepared. Applied. Thirty five days after the treatment, damage to mandarin orange squirrels on the distance from the cut surface and the developed leaves was investigated. Table 1 shows the survey results. As shown in Table 1, the penetrating insecticides acetamiprid and imidacloprid prevented the damage of citrus fruit moth, which occurs in shoots around the cut surface.

【0028】[0028]

【表1】 [Table 1]

【0029】試験例2 図2に示すように、青島温州を穂木とし、高接一挙更新
を実施し、接木部に接木テープを巻いた。約2か月後に
発芽した穂木のテープを切開し、接木部に薬剤を注入し
た。五日後にアブラムシ寄生芽率をを日本植物防疫協会
の基準に従って調査した。調査結果を第2表に示す。表
に示すように、発芽後のテープ切開時に一度接木部に注
入処理することによって、アブラムシ類(主要種:ワタ
アブラムシ)の防除が可能なことがわかった。
Test Example 2 As shown in FIG. 2, Aoshima Wenzhou was used as a scrub, and high-coupling was renewed all at once, and a graft tape was wrapped around the graft part. Approximately 2 months later, the tape of the sprouting buds was cut open, and the drug was injected into the graft. Five days later, the aphid parasitic bud rate was investigated according to the standards of the Japan Plant Protection Association. The survey results are shown in Table 2. As shown in the table, it was revealed that aphids (major species: cotton aphid) can be controlled by injecting the grafted part once at the time of tape cutting after germination.

【0030】[0030]

【表2】 [Table 2]

【0031】[0031]

【発明の効果】以上説明したように、本発明の薬剤組成
物は、柑橘類、例えば、温州みかんなどの夏期せん定の
切断面に塗布、あるいは接木処理部に注入処理するもの
であり、切断面あるいは接木処理部付近に生ずる新梢に
発生しやすい植物害虫に対し、極めて優れた防除効果を
有する。本発明の薬剤組成物は、酢酸ビニル系高分子を
含有することを特徴とする。このものは、(i)皮膜形
成性を有し、表面が乾燥することによって作業着に再付
着しないため作業効率がよい、(ii)降水や夜霧によっ
て再び柔らかくなり、有効成分が内部拡散することによ
って再び植物体に移行するという特徴を有するので、確
実かつ持続的な効果が期待できる。
As described above, the pharmaceutical composition of the present invention is applied to the cut surface of summer pruning such as citrus fruits, for example, Satsuma mandarin, or is injected into the grafting portion. It has an extremely excellent control effect against plant pests that tend to occur on new shoots near the grafted area. The pharmaceutical composition of the present invention is characterized by containing a vinyl acetate polymer. This product has (i) a film-forming property and has good work efficiency because it does not redeposit on work clothes due to surface drying. (Ii) It becomes soft again due to precipitation or night fog, and the active ingredient diffuses internally. Since it has a characteristic of being transferred to a plant again by the above, a reliable and lasting effect can be expected.

【図面の簡単な説明】[Brief description of drawings]

【図1】本発明の組成物の使用例。1 is an example of the use of the composition of the present invention.

【図2】本発明の組成物の使用例(接木処理)。FIG. 2 is an example of using the composition of the present invention (grafting treatment).

【符号の説明】 せん定の切断面 本発明の植物害虫防除剤組成物の入った容器 本発明の植物害虫防除剤組成物 新梢 接木処理部 接木テープ[Explanation of symbols] Cut surface of pruning Container containing the plant pest control composition of the present invention Plant pest control composition of the present invention New shoot grafting section Grafting tape

フロントページの続き (51)Int.Cl.6 識別記号 庁内整理番号 FI 技術表示箇所 A01N 37/34 101 A01N 37/34 101 37/52 37/52 43/40 101 43/40 101C 43/50 43/50 Q Z C 43/68 43/68 43/78 43/78 A Z 47/40 47/40 Z A 47/42 47/42 A 47/44 47/44 C08L 31/04 LHE C08L 31/04 LHE (72)発明者 宮田 明義 山口県大島郡橘町東安下庄 山口県大島柑 きつ試験場内 (72)発明者 斉藤 健志 東京都千代田区大手町2−2−1 日本曹 達株式会社内Continuation of front page (51) Int.Cl. 6 Identification code Office reference number FI Technical display location A01N 37/34 101 A01N 37/34 101 37/52 37/52 43/40 101 43/40 101C 43/50 43 / 50 Q Z C 43/68 43/68 43/78 43/78 A Z 47/40 47/40 Z A 47/42 47/42 A 47/44 47/44 C08L 31/04 LHE C08L 31/04 LHE (72) Inventor Akiyoshi Miyata Higashian Shimosho, Tachibana-cho, Oshima-gun, Yamaguchi Prefecture Oshima Kitsutsu Laboratory, Yamaguchi Prefecture (72) Inventor Kenji Saito 2-2-1 Otemachi, Chiyoda-ku, Tokyo Inside Nippon Soda Co., Ltd.

Claims (6)

【特許請求の範囲】[Claims] 【請求項1】浸透性殺虫剤および酢酸ビニル系高分子を
含有することを特徴とする、柑橘類害虫の防除剤組成
物。
1. A citrus pest control composition, which comprises a penetrating insecticide and a vinyl acetate polymer.
【請求項2】浸透性殺虫剤が、下記式〔I〕 【化1】 〔式中、Rは、水素原子、ホルミル基、アセチル基、C
1-4 アルキル基、2−クロロ−5−ピリジルメチル基又
は2−クロロ−5−チアゾリルメチル基を示し、Aは水
素原子、C1-4 アルキル基、Bと結合するエチレン基、
Bと結合するトリメチレン基又はBと結合する化2、 【化2】 で表される基を表す(R1 は水素原子又はC1-4 アルキ
ル基を表す。)。Bは、C1-4 アルキル基、SR2 (R
2 はC1-4 アルキル基を表す。)、化3、 【化3】 (R3 、R4 は、それぞれ水素原子、メチル基又はエチ
ル基を表す。)で表される基、Aと結合する−S−、A
と結合するメチレン基又はAと結合する化4、 【化4】 (R5 は水素原子又はC1-4 アルキル基を表す。)で表
される基を表す。Yは、N又はCR6 を示し(R6 は、
水素原子又はC1-4 アルキル基を表す。)、また、Xは
ニトロ基又はシアノ基を表す。〕で表される化合物であ
る請求項1記載の柑橘類害虫の防除剤組成物。
2. A systemic insecticide is represented by the following formula [I]: [In the formula, R represents a hydrogen atom, a formyl group, an acetyl group, C
1-4 alkyl group, 2-chloro-5-pyridylmethyl group or 2-chloro-5-thiazolylmethyl group, wherein A is a hydrogen atom, a C 1-4 alkyl group, an ethylene group bonded to B,
A trimethylene group that binds to B or a chemical formula that binds to B: Represents a group represented by (R 1 represents a hydrogen atom or a C 1-4 alkyl group). B is a C 1-4 alkyl group, SR 2 (R
2 represents a C 1-4 alkyl group. ), Chemical formula 3, (R 3, R 4 are each a hydrogen atom,. Represents methyl group or ethyl group) -S- bonded group represented by the A, A
A methylene group that binds to or a bond that binds to A, (R 5 represents a hydrogen atom or a C 1-4 alkyl group). Y represents N or CR 6 (R 6 is
It represents a hydrogen atom or a C 1-4 alkyl group. ), And X represents a nitro group or a cyano group. ] The control agent composition of the citrus pest of Claim 1 which is a compound represented by these.
【請求項3】剤中の浸透性殺虫剤の含有量が、0.1〜
10重量%である請求項1記載の柑橘類害虫の防除剤組
成物。
3. The content of the penetrating insecticide in the agent is 0.1 to 0.1.
The composition for controlling citrus pests according to claim 1, which is 10% by weight.
【請求項4】柑橘類のせん定をした切断面に請求項1に
記載の柑橘類害虫の防除剤組成物を塗布することを特徴
とする柑橘類害虫の防除方法。
4. A method for controlling citrus pests, which comprises applying the composition for controlling citrus pests according to claim 1 to a cut surface obtained by pruning citrus fruits.
【請求項5】浸透性殺菌剤および酢酸ビニル系高分子を
含有する組成物を、植物の接木処理部に注入することを
特徴とする植物害虫の防除方法。
5. A method for controlling plant pests, which comprises injecting a composition containing a penetrating bactericide and a vinyl acetate-based polymer into a plant grafting part.
【請求項6】浸透性殺菌剤および酢酸ビニル系高分子を
含有する組成物を、柑橘類植物の接木処理部に注入する
ことを特徴とする柑橘類害虫の防除方法。
6. A method for controlling citrus pests, which comprises injecting a composition containing a penetrating bactericide and a vinyl acetate-based polymer into a grafted portion of a citrus plant.
JP35443796A 1996-02-29 1996-12-19 Citrus pest control composition and control method Expired - Lifetime JP3965456B2 (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP35443796A JP3965456B2 (en) 1996-02-29 1996-12-19 Citrus pest control composition and control method

Applications Claiming Priority (3)

Application Number Priority Date Filing Date Title
JP8-69290 1996-02-29
JP6929096 1996-02-29
JP35443796A JP3965456B2 (en) 1996-02-29 1996-12-19 Citrus pest control composition and control method

Publications (2)

Publication Number Publication Date
JPH09291002A true JPH09291002A (en) 1997-11-11
JP3965456B2 JP3965456B2 (en) 2007-08-29

Family

ID=26410489

Family Applications (1)

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Country Link
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Cited By (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JP2007246495A (en) * 2006-03-20 2007-09-27 Mitsui Chemicals Inc Method for controlling disease and insect pest
JP2009073742A (en) * 2007-09-19 2009-04-09 Mitsui Chemicals Inc Method for controlling disease and pest
CN105993781A (en) * 2016-05-31 2016-10-12 陆川县银湖橘红种植专业合作社 Method for preventing pest and disease damages of exocarpium citri rubrum

Cited By (4)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JP2007246495A (en) * 2006-03-20 2007-09-27 Mitsui Chemicals Inc Method for controlling disease and insect pest
JP2009073742A (en) * 2007-09-19 2009-04-09 Mitsui Chemicals Inc Method for controlling disease and pest
CN105993781A (en) * 2016-05-31 2016-10-12 陆川县银湖橘红种植专业合作社 Method for preventing pest and disease damages of exocarpium citri rubrum
CN105993781B (en) * 2016-05-31 2018-12-04 陆川县银湖橘红种植专业合作社 A method of preventing Exocarpium Citri Rubrum pest and disease damage

Also Published As

Publication number Publication date
JP3965456B2 (en) 2007-08-29

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