JPS597101A - Attractant insecticide for controlling fruit fly - Google Patents
Attractant insecticide for controlling fruit flyInfo
- Publication number
- JPS597101A JPS597101A JP11559582A JP11559582A JPS597101A JP S597101 A JPS597101 A JP S597101A JP 11559582 A JP11559582 A JP 11559582A JP 11559582 A JP11559582 A JP 11559582A JP S597101 A JPS597101 A JP S597101A
- Authority
- JP
- Japan
- Prior art keywords
- insecticide
- water
- microcapsules
- attractant
- fruit flies
- Prior art date
- Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
- Granted
Links
Abstract
Description
【発明の詳細な説明】
本発明は、ミバエ類の防除に有用な誘引殺虫剤忙関する
ものである。さらに詳細には、本発明は
1)ミバエ類の誘引剤とミバエ類の殺虫剤の実質的に水
に不溶性の混合物を内相物とし、ゼラチンを主体とする
膜材で形成した平均粒径20〜150μの凝集型マイク
ロカプセル、2)水、
3)水の蒸発により成膜し、前記マイクロカプセルを植
物体に固着する能力のある高分子エマルジョン又は水浴
性ポリマー、(以後、固着剤と云う)
以上1)〜6)からなるミバエ類防除用誘引殺虫剤であ
る。DETAILED DESCRIPTION OF THE INVENTION The present invention relates to an insecticide attractant useful for controlling fruit flies. More specifically, the present invention provides 1) a material with an average particle size of 20 ml containing a substantially water-insoluble mixture of a fruit fly attractant and a fruit fly insecticide as an internal phase and formed of a membrane material mainly composed of gelatin. ~150μ aggregated microcapsules, 2) water, 3) a polymer emulsion or water-bathable polymer capable of forming a film by evaporation of water and fixing the microcapsules to plants (hereinafter referred to as a fixing agent). This is an attractive insecticide for controlling fruit flies consisting of the above 1) to 6).
本発明によれば、ミバエ類の防除を下記の点で効果的に
行なうことが出来る。According to the present invention, fruit flies can be effectively controlled in the following ways.
1)誘引剤と殺虫剤の混合物を内相物とするマイクロカ
プセル化剤のため、防除地域の115〜1/15程度の
面積に散布すればよい。1) Since it is a microencapsulated agent containing a mixture of an attractant and an insecticide as its internal phase, it can be sprayed over an area approximately 115 to 1/15 of the area to be controlled.
++)水に懸濁したマイクロカプセル剤であるため、空
中散布に適しており、ドリフトが少ない。++) Since it is a microcapsule suspended in water, it is suitable for aerial spraying and has little drift.
111)平均粒径20〜150μの凝集型のマイクロカ
プセル剤で、かつ固着剤を使用しているため、乳剤にく
らべて残効性に優れている。111) Since it is an agglomerated microcapsule with an average particle size of 20 to 150 μm and uses a fixing agent, it has excellent residual effect compared to emulsions.
以上の様な、特長、利点があるために、ウリミバエ、ミ
カンコミバエ、地中海ミバエなどのミバエ類の防除に用
いることが出来、かつミバエ類の防除を効果的に行な5
ことが出来る。Because of the above features and advantages, it can be used to control fruit flies such as the melon fruit fly, citrus fruit fly, and Mediterranean fruit fly, and it can be used to effectively control fruit flies.
I can do it.
これに使用する誘引剤および殺虫剤としては通常公知の
薬剤が使用され、好ましくは次のものを挙げることが出
来る。尚これらにおいて〔〕の中は化学名を表わし、〔
〕の前の名称は商品名を示す。As attractants and insecticides used for this purpose, commonly known agents are used, and preferably the following can be mentioned. In these, the characters in [ ] represent the chemical name, and [
The name before ] indicates the product name.
即ちミバエ類の誘引剤としては、ウリミバエに対しては
キュウルア[4−(p−アセトキシフェニル)−2−ブ
タノン〕、ミカンコミバエに対してはメチルオイゲノー
ル、地中海ミバエに対し【はメトルーア(5ec−ブチ
ル−1rans −4(or5)クロロ−2−メチルシ
クロヘキサン−1−カルボキシレート〕、トリメトルー
ア(tert−ブチル−1rans −4(or 5
)クロロ−2−メチルシクロヘキサン−1−カルボキシ
レート〕等、ミバエ類の殺虫剤としては、多くのものが
知られ【いるが、例えばスミチオン(0,0−ジメチル
−〇−(3−メチル−4−二トロフェニル)チオホスフ
ェート〕、マラソン(0,0−ジメチル−8−(1,2
−ジカルポエトキシメチル)ジチオホスフェート、ジブ
ロム〔ジメチル−1,2−ジブロム−2,2−ジクロロ
エチルホスフェート〕すどが通常使用される。That is, as attractants for fruit flies, cuurua [4-(p-acetoxyphenyl)-2-butanone] is used for the medicinal fruit fly, methyleugenol is used for the orange fruit fly, and metrua (5ec-butyl-) is used for the Mediterranean fruit fly. 1rans-4(or5) chloro-2-methylcyclohexane-1-carboxylate], trimetroua(tert-butyl-1rans-4(or 5)
) Chloro-2-methylcyclohexane-1-carboxylate] Many insecticides for fruit flies are known, such as sumithion (0,0-dimethyl-〇-(3-methyl-4 -nitrophenyl)thiophosphate], marathon (0,0-dimethyl-8-(1,2
-dicarpoethoxymethyl)dithiophosphate, dibromo[dimethyl-1,2-dibromo-2,2-dichloroethylphosphate]sudo are commonly used.
これら誘引剤及び殺虫剤を選択する場合は、ミバエ類に
有効であることの他に、誘引剤と殺で
虫削が好ましくは1:9〜9:1の割合で均一に混合し
、その混合物が実質的に水に不溶であることが必要であ
る。When selecting these attractants and insecticides, in addition to being effective against fruit flies, the attractants and insecticides should be mixed uniformly in a ratio of preferably 1:9 to 9:1, and the mixture should be is substantially insoluble in water.
誘引剤と殺虫剤の混合割合は、防除効果が最も発揮で、
きる様に選らべばよい。The mixing ratio of attractant and insecticide is the one that has the best control effect.
You just have to choose as you see fit.
この混合割合が前記範囲を外れると誘引と殺虫のいずれ
かの効果に偏りが出来、優れた防除効果が得られないお
それがあり、特に好ましくは2:8〜8:2がよい。If this mixing ratio is out of the above range, either the attraction or insecticidal effects will be biased, and there is a risk that an excellent pesticidal effect may not be obtained. Particularly preferably, the mixing ratio is 2:8 to 8:2.
誘引剤と殺虫剤の混合物を内相物と1−るマイクロカプ
セルは、ゼラチンを主体とする膜材な有するもので、水
溶液からのコンプレックス、コアセルベーション法で製
造することが出来る。Microcapsules containing a mixture of an attractant and an insecticide as an internal phase have a gelatin-based membrane material, and can be produced by a complex or coacervation method from an aqueous solution.
ゼラチンとコアセルベートを作る化合物としては、アラ
ビヤゴム、カラーギーナン、カルボキシメチルセルロー
ス、ポリアクリル酸ソーダ、マレイン酸共重合体、ヘキ
サメタリン酸ソーダなどが知られている。例えば、US
P2,800,457、U8P2,800,458、B
Pl、117,178、特公昭48−17985などに
示された公知の方法に従って製造することが出来る。Known compounds that make gelatin and coacervate include gum arabic, carrageenan, carboxymethylcellulose, sodium polyacrylate, maleic acid copolymer, and sodium hexametaphosphate. For example, U.S.
P2,800,457, U8P2,800,458, B
Pl, 117,178, Japanese Patent Publication No. 48-17985, and the like.
本発明では、空中散布に使用してドリフト防止効果があ
ること、残効性が発揮できることなどより、平均粒径2
0〜150μの凝集型のマイクロカプセルを使用する。In the present invention, the average particle size of 2
Agglomerated microcapsules of 0 to 150μ are used.
誘引剤と殺虫剤の混合物である内相物オイルを2〜10
μに分散して、カプセル化条件、例えばPH1温度など
を適切に選ぶことにより平均粒径20〜150μの凝集
型のマイクロカプセルを製造することが出来る。2 to 10% of internal phase oil, which is a mixture of attractant and insecticide.
By appropriately selecting the encapsulation conditions such as PH1 temperature, agglomerated microcapsules with an average particle size of 20 to 150 μ can be produced.
このマイクロカプセルの平均粒径が20μ未満の場合に
は、ドリフトしやすくなる他に、残効性も低くなるため
好ましくなく、平均粒径が150μを越えると、農薬の
局在化による薬効の低下をきたすと共に、空中散布装置
のノズルを閉塞する危険性が生ずる。これらのことから
30〜100μの範囲が特に好ましい。If the average particle size of the microcapsules is less than 20μ, it is undesirable because it tends to drift and has a low residual effect.If the average particle size exceeds 150μ, the localization of the pesticide reduces its efficacy. In addition, there is a risk of clogging the nozzle of the aerial spraying device. For these reasons, a range of 30 to 100 μm is particularly preferable.
水溶液からの相分離法により製造した本発明に用いるマ
イクロカプセルは、水にマイクロカプセルが懸濁した状
態で°あり、これに固着剤として水の蒸発により成膜す
る高分子エマルジョン又は水溶性ポリマーを添加する。The microcapsules used in the present invention produced by phase separation from an aqueous solution are in a state in which the microcapsules are suspended in water, and a polymer emulsion or water-soluble polymer, which is formed into a film by evaporation of water, is added as a fixing agent to the microcapsules. Added.
高分子エマルジョンとしては%開昭56−11883に
示した様な、アクリル系や酢酸ビニル系のエマルジョン
を用いることが出来る。As the polymer emulsion, an acrylic emulsion or a vinyl acetate emulsion as shown in 11883/1983 can be used.
水浴性ポリマーとしては、ポリビニルアルコール、ポリ
アクリル酸ソーダ、ポリビニルピロリドン、キサノタン
ガムなどを用いることが出来る、
これら固着剤の使用量は、マイクロカプセルに対し固型
分として5〜30重量%が適当である。この固着剤は植
物体にマイクロカプセルを固着し、雨や風により落下し
ない様にするため釦用いる。従って固着剤を使用するこ
とにより、農薬の有効利用がはかれると共に、残効性を
高めることも出来るのである。As the water bathing polymer, polyvinyl alcohol, sodium polyacrylate, polyvinylpyrrolidone, xanothane gum, etc. can be used. The appropriate amount of these fixing agents used is 5 to 30% by weight of the solid content based on the microcapsules. . This fixing agent is used to fix the microcapsules to the plant body and to prevent them from falling off due to rain and wind. Therefore, by using a fixing agent, agricultural chemicals can be used more effectively and their residual effectiveness can be increased.
また、この固着剤はあらかじめ添加しておい【もよいし
、散布直前に添加してもよい。Further, this fixing agent may be added in advance or may be added immediately before spraying.
この誘引殺虫剤に、必要に応じて次の化合物を添加する
ことが出来る。The following compounds can be added to this insecticide attractant as necessary.
■ マイクロカプセルの分散性を高めるためのポリアク
リル醒ソーダ、クレイなどの分教剤■ 水層の表面張力
を低下させて、農薬の付着量を増大させるための界面活
性剤、
■ 水浴液の誘引剤であるブロテイノなと、本発明のマ
イクロカプセルは、ゼラチンを主体とする膜材を有する
凝集型であるが、ゼラチン系膜を用いることは次の利点
があり、
:)安全性が高く、自然界で分解しやすい。■ Dispersing agents such as polyacrylic soda and clay to improve the dispersibility of microcapsules ■ Surfactants to reduce the surface tension of the water layer and increase the amount of pesticides attached ■ Attracting water bath liquid The microcapsules of the present invention are agglomerated with a gelatin-based membrane, but the use of a gelatin membrane has the following advantages::) It is highly safe and naturally occurring. Easy to disassemble.
il)水と接触することにまり良薬を徐々に溶出する。il) Gradual elution of the drug on contact with water.
II)農薬の光による分解を防止し、気散を防ぐ1■)
ゼラチンを用いるコアセルベーション法は工業的に確立
された安定したマイクロカプセルの製造法である。II) Preventing the decomposition of pesticides by light and preventing their dispersion 1■)
The coacervation method using gelatin is an industrially established method for producing stable microcapsules.
また凝集型であることは、次の利点を有する。Furthermore, being an agglomerated type has the following advantages.
I)表面積が大きく溶出しやすいため、初期の薬効が高
い。I) It has a large surface area and is easily eluted, so it has high initial efficacy.
11)植物体に対する付着性が単核型のマイクロカプセ
ルよりは優れている。11) Better adhesion to plants than mononuclear microcapsules.
1ll)同じ平均粒径の単核型のマイクロカプセルにく
らべて残効性に優れている、
+V)粒度分布のせまいマイクロカプセルが、単核型の
場合にくらべて作り易い。1ll) Superior residual efficacy compared to mononuclear type microcapsules with the same average particle size; +V) Microcapsules with a narrow particle size distribution are easier to produce than mononuclear type.
実際に散布する場合は、所定の原料濃度に水で希釈して
散布することが出来、空中散布の場合通常は1ヘクター
ル当り81−501の液量な散布する。この場合、誘引
殺虫剤であるため、防除面積の115〜1/15に点散
布すればよいため効率的であると共に、単位面積当りの
投下薬量も低くなり、危被害防止となる。When actually spraying, the material can be diluted with water to a predetermined raw material concentration before being sprayed, and in the case of aerial spraying, it is usually sprayed at a liquid volume of 81 to 50 parts per hectare. In this case, since it is an attractant insecticide, it is efficient because it only needs to be sprayed pointwise over 115 to 1/15 of the area to be controlled, and the amount of sprayed per unit area is also low, which prevents damage.
げる。Geru.
実施例1
スミチオン/キュウルア=+o15[:重量比〕を内相
物とする平均粒径100μの凝集型マイクロカプセルを
特公昭4B−17985の実施例1に準じて製造した。Example 1 Agglomerated microcapsules having an average particle size of 100 μm and containing Sumithion/Cuurua=+o15 [: weight ratio] as the internal phase were produced according to Example 1 of Japanese Patent Publication No. 4B-17985.
この場合の内相物オイルの平均粒径は8μで、膜材料は
内相物の20重量%である。In this case, the average particle size of the internal phase oil was 8 microns, and the membrane material was 20% by weight of the internal phase.
屋外の綱室中夫に鉢植ミカン本を置き、これに次の組成
の誘引殺虫剤をスプレーした。A potted tangerine plant was placed in the outdoor rope room, and an insecticide with the following composition was sprayed on it.
Xtチ 乾燥後、人工飼料で飼育したウリミノ(工を放飼した。Xt Chi After drying, the uriminos reared on artificial feed were released.
24時間後の誘引殺虫効果を検討したところ、15日後
まで誘引殺虫効果を示した。When the insecticidal effect was examined after 24 hours, the insecticidal effect was observed until 15 days later.
比較例1
単核型マイクロカプセルにする以外は、実施例1と同様
に誘引殺虫剤を調合し、24時間後の誘引殺虫効果を検
討したところ、10日後は誘引殺虫効果を示さなかった
。Comparative Example 1 An attracting insecticide was prepared in the same manner as in Example 1 except that it was made into mononuclear microcapsules, and the attracting insecticidal effect was examined after 24 hours. As a result, no attracting insecticidal effect was shown after 10 days.
実施例2
スミチオン/メチルオイゲノール=1015〔重量比〕
を内相物とする平均粒径50μの凝集型マイクロカプセ
ルを特公昭48−17985の実施例1に準じて製造し
た。この場合の内相物オイルの平均粒径は5μで、膜材
料は内相物の10M、量チである。次の組成の誘引殺虫
剤はミカンコミバエに対して誘引殺虫効果を示した。Example 2 Sumithion/methyleugenol = 1015 [weight ratio]
Agglomerated microcapsules having an average particle size of 50 μm and having the internal phase substance were produced according to Example 1 of Japanese Patent Publication No. 17985/1983. In this case, the average particle diameter of the internal phase oil was 5 μm, and the membrane material was 10 M, the amount of the internal phase oil. The attracting insecticide with the following composition showed attracting and killing effects on Citrus fruit fly.
重量%
実施例6
マラソン/トリメトルーア=4/6 (重量比〕を内相
物とする平均粒径50μの凝集型マイクロカプセルを、
特公昭4B−17985の実施例1に準じて製造した。Weight % Example 6 Agglomerated microcapsules with an average particle size of 50 μm containing Marathon/Trimetrore = 4/6 (weight ratio) as the internal phase,
It was manufactured according to Example 1 of Japanese Patent Publication No. 4B-17985.
この場合の内相物オイルの平均粒径は5μで、膜材料は
内相物の20重量%である。In this case, the average particle size of the internal phase oil was 5 μm, and the membrane material was 20% by weight of the internal phase.
次の組成の誘引殺虫剤は、地中海ミバエに対して、誘引
殺虫効果を示した。The attracting insecticide having the following composition showed attracting and killing effects on the Mediterranean fruit fly.
重音、チ
実施例4
スミチオン/キュツルア=I 015(3H1比〕を内
相物とする20〜80μの凝集型マイクロカプセルを特
公昭48−17985の実施例1に準じて製造した。Example 4 Agglomerated microcapsules of 20 to 80 μm containing Sumithion/Cuturua I 015 (3H1 ratio) as the internal phase were produced according to Example 1 of Japanese Patent Publication No. 17985/1985.
この場合の内相物のオイル粒径は4〜6μで、膜材料は
内相物の12重量%である。In this case, the oil particle size of the internal phase is 4 to 6 microns, and the membrane material is 12% by weight of the internal phase.
医の組成の誘引殺虫剤を調合し、ヘリコプタ−によりウ
リミバエ生息地に1/10の点数布を行なった。散布量
は81/ha である。A medically formulated attractant and insecticide was prepared, and a 1/10-spot distribution was carried out on the melon fly habitat using a helicopter. The application rate was 81/ha.
散布の結果、散布地域は15日間ウリミバエの密度低下
を示した。As a result of the spraying, the sprayed area showed a decrease in the density of the fruit fly for 15 days.
特許出願人の名称 東亜合成化学工業株式会社 社団法人農林水産航空協会 APatent applicant name Toagosei Chemical Industry Co., Ltd. Agriculture, Forestry and Fisheries Aviation Association A
Claims (1)
的に水に不溶性の混合物を内相物とし、ゼラチンを主体
とする膜材で形成した平均粒径20〜150μの凝集型
マイクロカプセル、 2)水、 3)水の蒸発により成膜し、前記マイクロカプセルを植
物体に固着する能力のある高分子エマルジョン、又は水
溶性ポリマー、以上υ〜3)かもなるミバエ類防除用誘
引殺虫剤。[Scope of Claims] t. An average particle size of 20 to 20, which is formed from a film material mainly composed of gelatin, with an internal phase containing a substantially water-insoluble mixture of a fruit fly attractant and a fruit fly insecticide. Agglomerated microcapsules of 150μ, 2) water, 3) a polymer emulsion or water-soluble polymer capable of forming a film by evaporation of water and fixing the microcapsules to the plant body, and the above υ~3) are also fruit flies. Attractive insecticide for controlling insects.
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP11559582A JPS597101A (en) | 1982-07-05 | 1982-07-05 | Attractant insecticide for controlling fruit fly |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP11559582A JPS597101A (en) | 1982-07-05 | 1982-07-05 | Attractant insecticide for controlling fruit fly |
Publications (2)
Publication Number | Publication Date |
---|---|
JPS597101A true JPS597101A (en) | 1984-01-14 |
JPS6312441B2 JPS6312441B2 (en) | 1988-03-18 |
Family
ID=14666495
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
JP11559582A Granted JPS597101A (en) | 1982-07-05 | 1982-07-05 | Attractant insecticide for controlling fruit fly |
Country Status (1)
Country | Link |
---|---|
JP (1) | JPS597101A (en) |
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JPS6366102A (en) * | 1986-07-09 | 1988-03-24 | モンサント カンパニ− | Water-dispersible granules and manufacture |
JPH02289502A (en) * | 1989-03-17 | 1990-11-29 | Albright & Wilson Ltd | Suspension containing biocidal agent |
WO2009011537A3 (en) * | 2007-07-19 | 2009-03-19 | Nat Univ Chungbuk Ind Acad | Physical control agents and control method from water-soluble polymer against small-size insect pests |
JP2010509330A (en) * | 2006-11-07 | 2010-03-25 | ダウ アグロサイエンシィズ エルエルシー | Dispersible sustained release male removal method (MAT) formulation and insect control method |
JP2019011340A (en) * | 2010-06-08 | 2019-01-24 | ダウ アグロサイエンシィズ エルエルシー | Microencapsulated oil for controlling spray drift of pesticide |
EP3384773A4 (en) * | 2015-11-30 | 2019-04-24 | Kumiai Chemical Industry Co., Ltd. | Aqueous agrochemical suspension composition and dispersal method therefor |
CN110250174A (en) * | 2018-03-12 | 2019-09-20 | 山东侨昌现代农业有限公司 | A kind of oil-containing dry suspending agent dosage form and processing technology |
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CN108094356A (en) * | 2015-07-16 | 2018-06-01 | 安溪县智睿电子商务有限公司 | A kind of drosophila trap setting |
CN110583636A (en) * | 2018-06-13 | 2019-12-20 | 江苏龙灯化学有限公司 | Pesticide adjuvant suitable for agriculture and application thereof |
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JPS511645A (en) * | 1974-06-26 | 1976-01-08 | Sanyo Chemical Ind Ltd | Noyakuno koryokujizokuhoho |
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Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPS50135232A (en) * | 1974-04-01 | 1975-10-27 | ||
JPS511645A (en) * | 1974-06-26 | 1976-01-08 | Sanyo Chemical Ind Ltd | Noyakuno koryokujizokuhoho |
JPS52145518A (en) * | 1976-04-09 | 1977-12-03 | Herculite Protective Fab | Dispenser |
JPS5589201A (en) * | 1978-12-28 | 1980-07-05 | Nakanihon Koku Kk | Vermin extermination and its device with aerial application or release of attractant and aerial dusting of insecticide |
Cited By (9)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPS6366102A (en) * | 1986-07-09 | 1988-03-24 | モンサント カンパニ− | Water-dispersible granules and manufacture |
JPH02289502A (en) * | 1989-03-17 | 1990-11-29 | Albright & Wilson Ltd | Suspension containing biocidal agent |
JP2010509330A (en) * | 2006-11-07 | 2010-03-25 | ダウ アグロサイエンシィズ エルエルシー | Dispersible sustained release male removal method (MAT) formulation and insect control method |
WO2009011537A3 (en) * | 2007-07-19 | 2009-03-19 | Nat Univ Chungbuk Ind Acad | Physical control agents and control method from water-soluble polymer against small-size insect pests |
JP2019011340A (en) * | 2010-06-08 | 2019-01-24 | ダウ アグロサイエンシィズ エルエルシー | Microencapsulated oil for controlling spray drift of pesticide |
EP3384773A4 (en) * | 2015-11-30 | 2019-04-24 | Kumiai Chemical Industry Co., Ltd. | Aqueous agrochemical suspension composition and dispersal method therefor |
US10440949B2 (en) | 2015-11-30 | 2019-10-15 | Kumiai Chemical Industry Co., Ltd. | Aqueous agrochemical suspension composition and dispersal method therefor |
CN110250174A (en) * | 2018-03-12 | 2019-09-20 | 山东侨昌现代农业有限公司 | A kind of oil-containing dry suspending agent dosage form and processing technology |
CN110250174B (en) * | 2018-03-12 | 2022-08-19 | 侨昌现代农业有限公司 | Oil-containing dry suspending agent formulation and processing technology thereof |
Also Published As
Publication number | Publication date |
---|---|
JPS6312441B2 (en) | 1988-03-18 |
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