CN115956568B - A kind of bactericidal composition containing flutriafol - Google Patents
A kind of bactericidal composition containing flutriafol Download PDFInfo
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- 239000005787 Flutriafol Substances 0.000 title claims abstract description 56
- JWUCHKBSVLQQCO-UHFFFAOYSA-N 1-(2-fluorophenyl)-1-(4-fluorophenyl)-2-(1H-1,2,4-triazol-1-yl)ethanol Chemical compound C=1C=C(F)C=CC=1C(C=1C(=CC=CC=1)F)(O)CN1C=NC=N1 JWUCHKBSVLQQCO-UHFFFAOYSA-N 0.000 title claims abstract description 54
- 239000000203 mixture Substances 0.000 title claims abstract description 24
- 230000000844 anti-bacterial effect Effects 0.000 title description 2
- 241000209140 Triticum Species 0.000 claims abstract description 18
- 230000000855 fungicidal effect Effects 0.000 claims abstract description 18
- 235000021307 Triticum Nutrition 0.000 claims abstract description 17
- 241000223218 Fusarium Species 0.000 claims abstract description 15
- 239000000417 fungicide Substances 0.000 claims abstract description 14
- UHPMCKVQTMMPCG-UHFFFAOYSA-N 5,8-dihydroxy-2-methoxy-6-methyl-7-(2-oxopropyl)naphthalene-1,4-dione Chemical compound CC1=C(CC(C)=O)C(O)=C2C(=O)C(OC)=CC(=O)C2=C1O UHPMCKVQTMMPCG-UHFFFAOYSA-N 0.000 claims abstract description 12
- 206010039509 Scab Diseases 0.000 claims 1
- TWFZGCMQGLPBSX-UHFFFAOYSA-N Carbendazim Natural products C1=CC=C2NC(NC(=O)OC)=NC2=C1 TWFZGCMQGLPBSX-UHFFFAOYSA-N 0.000 abstract description 22
- 239000006013 carbendazim Substances 0.000 abstract description 22
- JNPZQRQPIHJYNM-UHFFFAOYSA-N carbendazim Chemical compound C1=C[CH]C2=NC(NC(=O)OC)=NC2=C1 JNPZQRQPIHJYNM-UHFFFAOYSA-N 0.000 abstract description 21
- 239000003795 chemical substances by application Substances 0.000 abstract description 13
- 239000005843 Thiram Substances 0.000 abstract description 11
- 230000002195 synergetic effect Effects 0.000 abstract description 11
- KUAZQDVKQLNFPE-UHFFFAOYSA-N thiram Chemical compound CN(C)C(=S)SSC(=S)N(C)C KUAZQDVKQLNFPE-UHFFFAOYSA-N 0.000 abstract description 11
- 229960002447 thiram Drugs 0.000 abstract description 11
- 230000000694 effects Effects 0.000 abstract description 6
- 244000052769 pathogen Species 0.000 abstract description 6
- 239000000575 pesticide Substances 0.000 abstract description 5
- 230000009471 action Effects 0.000 abstract description 4
- 230000002401 inhibitory effect Effects 0.000 abstract description 4
- 206010034133 Pathogen resistance Diseases 0.000 abstract description 2
- 238000011161 development Methods 0.000 abstract description 2
- 230000007246 mechanism Effects 0.000 abstract description 2
- 239000003814 drug Substances 0.000 description 9
- 241000223195 Fusarium graminearum Species 0.000 description 8
- 229940079593 drug Drugs 0.000 description 8
- 230000001988 toxicity Effects 0.000 description 7
- 231100000419 toxicity Toxicity 0.000 description 7
- 208000037265 diseases, disorders, signs and symptoms Diseases 0.000 description 5
- 238000000034 method Methods 0.000 description 5
- 208000001840 Dandruff Diseases 0.000 description 4
- 230000001580 bacterial effect Effects 0.000 description 4
- 238000004519 manufacturing process Methods 0.000 description 4
- 230000002265 prevention Effects 0.000 description 4
- 238000012360 testing method Methods 0.000 description 4
- 208000031888 Mycoses Diseases 0.000 description 3
- 201000010099 disease Diseases 0.000 description 3
- 230000006872 improvement Effects 0.000 description 3
- 238000011282 treatment Methods 0.000 description 3
- IAZDPXIOMUYVGZ-UHFFFAOYSA-N Dimethylsulphoxide Chemical compound CS(C)=O IAZDPXIOMUYVGZ-UHFFFAOYSA-N 0.000 description 2
- 239000005783 Fluopyram Substances 0.000 description 2
- 239000013043 chemical agent Substances 0.000 description 2
- 238000013329 compounding Methods 0.000 description 2
- KVDJTXBXMWJJEF-UHFFFAOYSA-N fluopyram Chemical compound ClC1=CC(C(F)(F)F)=CN=C1CCNC(=O)C1=CC=CC=C1C(F)(F)F KVDJTXBXMWJJEF-UHFFFAOYSA-N 0.000 description 2
- 230000009036 growth inhibition Effects 0.000 description 2
- 239000000243 solution Substances 0.000 description 2
- PXMNMQRDXWABCY-UHFFFAOYSA-N 1-(4-chlorophenyl)-4,4-dimethyl-3-(1H-1,2,4-triazol-1-ylmethyl)pentan-3-ol Chemical compound C1=NC=NN1CC(O)(C(C)(C)C)CCC1=CC=C(Cl)C=C1 PXMNMQRDXWABCY-UHFFFAOYSA-N 0.000 description 1
- 235000017060 Arachis glabrata Nutrition 0.000 description 1
- 244000105624 Arachis hypogaea Species 0.000 description 1
- 235000010777 Arachis hypogaea Nutrition 0.000 description 1
- 235000018262 Arachis monticola Nutrition 0.000 description 1
- 241000235349 Ascomycota Species 0.000 description 1
- 208000035143 Bacterial infection Diseases 0.000 description 1
- 241000221198 Basidiomycota Species 0.000 description 1
- 241000207199 Citrus Species 0.000 description 1
- 241000221785 Erysiphales Species 0.000 description 1
- 235000007688 Lycopersicon esculentum Nutrition 0.000 description 1
- 239000005868 Metconazole Substances 0.000 description 1
- 240000007594 Oryza sativa Species 0.000 description 1
- 235000007164 Oryza sativa Nutrition 0.000 description 1
- 239000005820 Prochloraz Substances 0.000 description 1
- 240000003768 Solanum lycopersicum Species 0.000 description 1
- 229930182558 Sterol Natural products 0.000 description 1
- 239000005839 Tebuconazole Substances 0.000 description 1
- 230000000996 additive effect Effects 0.000 description 1
- 230000003042 antagnostic effect Effects 0.000 description 1
- 239000007864 aqueous solution Substances 0.000 description 1
- 244000052616 bacterial pathogen Species 0.000 description 1
- 230000009286 beneficial effect Effects 0.000 description 1
- 238000009395 breeding Methods 0.000 description 1
- 230000001488 breeding effect Effects 0.000 description 1
- 210000002421 cell wall Anatomy 0.000 description 1
- 235000020971 citrus fruits Nutrition 0.000 description 1
- 239000002131 composite material Substances 0.000 description 1
- 150000001875 compounds Chemical class 0.000 description 1
- 238000007405 data analysis Methods 0.000 description 1
- 230000003247 decreasing effect Effects 0.000 description 1
- 230000017858 demethylation Effects 0.000 description 1
- 238000010520 demethylation reaction Methods 0.000 description 1
- 238000001514 detection method Methods 0.000 description 1
- 238000005516 engineering process Methods 0.000 description 1
- 230000008686 ergosterol biosynthesis Effects 0.000 description 1
- 230000002538 fungal effect Effects 0.000 description 1
- 230000036541 health Effects 0.000 description 1
- 239000003112 inhibitor Substances 0.000 description 1
- JEIPFZHSYJVQDO-UHFFFAOYSA-N iron(III) oxide Inorganic materials O=[Fe]O[Fe]=O JEIPFZHSYJVQDO-UHFFFAOYSA-N 0.000 description 1
- 238000012417 linear regression Methods 0.000 description 1
- 238000005259 measurement Methods 0.000 description 1
- XWPZUHJBOLQNMN-UHFFFAOYSA-N metconazole Chemical compound C1=NC=NN1CC1(O)C(C)(C)CCC1CC1=CC=C(Cl)C=C1 XWPZUHJBOLQNMN-UHFFFAOYSA-N 0.000 description 1
- 239000002636 mycotoxin Substances 0.000 description 1
- 230000001717 pathogenic effect Effects 0.000 description 1
- 235000020232 peanut Nutrition 0.000 description 1
- 235000010482 polyoxyethylene sorbitan monooleate Nutrition 0.000 description 1
- 229920000053 polysorbate 80 Polymers 0.000 description 1
- TVLSRXXIMLFWEO-UHFFFAOYSA-N prochloraz Chemical compound C1=CN=CN1C(=O)N(CCC)CCOC1=C(Cl)C=C(Cl)C=C1Cl TVLSRXXIMLFWEO-UHFFFAOYSA-N 0.000 description 1
- 230000001681 protective effect Effects 0.000 description 1
- 230000009467 reduction Effects 0.000 description 1
- 235000009566 rice Nutrition 0.000 description 1
- 238000012216 screening Methods 0.000 description 1
- 238000001228 spectrum Methods 0.000 description 1
- 238000007619 statistical method Methods 0.000 description 1
- 235000003702 sterols Nutrition 0.000 description 1
- 239000011550 stock solution Substances 0.000 description 1
- 239000000126 substance Substances 0.000 description 1
- 238000010998 test method Methods 0.000 description 1
- 230000001225 therapeutic effect Effects 0.000 description 1
- 230000002110 toxicologic effect Effects 0.000 description 1
- 231100000027 toxicology Toxicity 0.000 description 1
- -1 triazole sterol Chemical class 0.000 description 1
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- Y—GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
- Y02—TECHNOLOGIES OR APPLICATIONS FOR MITIGATION OR ADAPTATION AGAINST CLIMATE CHANGE
- Y02A—TECHNOLOGIES FOR ADAPTATION TO CLIMATE CHANGE
- Y02A50/00—TECHNOLOGIES FOR ADAPTATION TO CLIMATE CHANGE in human health protection, e.g. against extreme weather
- Y02A50/30—Against vector-borne diseases, e.g. mosquito-borne, fly-borne, tick-borne or waterborne diseases whose impact is exacerbated by climate change
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Abstract
本发明属于农药技术领域,具体属于一种含粉唑醇的杀菌组合物。一种含粉唑醇的杀菌组合物,其由粉唑醇和多菌灵、福美双或烯肟菌胺复配而成。本发明杀菌组合物中粉唑醇和多菌灵、福美双或烯肟菌胺的作用机理不同,在进行组合使用时,可以从不同的作用位点抑制病原菌,进而可以延缓病原菌抗性发展,延长药剂的使用寿命。另外,本发明杀菌组合物对抑制小麦赤霉病病原菌表现出增效作用,可以提高对小麦赤霉病的防治效果,进而可以降低农药的施用剂量,减少防治成本。The present invention belongs to the technical field of pesticides, and specifically belongs to a fungicide composition containing flutriafol. A fungicide composition containing flutriafol is compounded with flutriafol and carbendazim, thiram or enoxamyl. The fungicide composition of the present invention has different action mechanisms from carbendazim, thiram or enoxamyl. When used in combination, the fungicide composition can inhibit pathogens from different action sites, thereby delaying the development of pathogen resistance and extending the service life of the agent. In addition, the fungicide composition of the present invention shows a synergistic effect on inhibiting wheat fusarium head blight pathogens, can improve the control effect of wheat fusarium head blight, thereby reducing the application dosage of pesticides and reducing the control cost.
Description
技术领域Technical Field
本发明属于农药技术领域,具体属于一种含粉唑醇的杀菌组合物。The invention belongs to the technical field of pesticides, and in particular belongs to a fungicide composition containing flutriafol.
背景技术Background Art
赤霉病、白粉病、纹枯病、锈病和叶枯病等病害是威胁小麦生产的重要真菌性病害。其中,小麦赤霉病主要是由禾谷镰孢菌(Fusarium graminearunm)引起的小麦病害。小麦赤霉病的发生不仅会造成小麦减产,还因产真菌毒素造成小麦品质下降,影响食用者的健康。Fusarium fusarium, powdery mildew, sheath blight, rust and leaf blight are important fungal diseases that threaten wheat production. Among them, wheat fusarium fusarium is mainly caused by Fusarium graminearum. The occurrence of wheat fusarium fusarium not only causes a reduction in wheat production, but also reduces wheat quality due to the production of fungal toxins, affecting the health of consumers.
在实际生产过程中,防治小麦赤霉病主要采用以抗病品种为基础,以药剂防治为重点的综合防治方法。但抗病品种的选育存在抗性改良周期长和高效抗性种植资源缺乏等一些列问题,使得化学药剂仍是防治小麦赤霉病的中药手段。防治小麦赤霉病的常用药剂有:多菌灵、叶菌唑、戊唑醇和咪鲜胺等,但由于多年连续使用,抗性问题发展迅速,抗性菌株检出率急剧上升,导致防效逐年下降。因此,开发新的替代药剂或新复配剂很有必要。In the actual production process, the prevention and control of wheat fusarium head blight mainly adopts a comprehensive prevention and control method based on disease-resistant varieties and focusing on chemical control. However, the breeding of disease-resistant varieties has a series of problems such as a long resistance improvement cycle and a lack of high-efficiency resistance planting resources, which makes chemical agents still the traditional Chinese medicine means of preventing and controlling wheat fusarium head blight. Commonly used agents for the prevention and control of wheat fusarium head blight include: carbendazim, metconazole, tebuconazole and prochloraz, but due to years of continuous use, the resistance problem has developed rapidly, the detection rate of resistant strains has increased sharply, and the prevention effect has decreased year by year. Therefore, it is necessary to develop new alternative agents or new compound agents.
粉唑醇是先正达集团股份有限公司开发的三唑类甾醇脱甲基化抑制剂类杀菌剂。粉唑醇可有效抑制麦角甾醇的生物合成,并造成真菌细胞壁的破裂,具有广谱的抑菌活性和较强的内吸性,且对担子菌和子囊菌引起的许多真菌病害均具有良好的保护和治疗作用。CN201410788209.9,公开了一种含甲磺酰菌唑和粉唑醇的复配组合物及杀菌剂,并具体公开了甲磺酰菌唑和粉唑醇复配后可用于防治细菌性和真菌性病害,如水稻细菌性条斑病、柑橘溃疡病、番茄青枯病和花生叶斑病等。另外,CN201310061385.8,还公开了一种含氟嘧菌胺的杀菌组合物,并具体公开了氟嘧菌胺和粉唑醇复配后对多种作物上的多种病害都有较高活性,并具有明显的增效作用,扩大的杀菌谱。Flutriafol is a triazole sterol demethylation inhibitor fungicide developed by Syngenta Group Co., Ltd. Flutriafol can effectively inhibit the biosynthesis of ergosterol and cause the rupture of fungal cell walls. It has a broad spectrum of antibacterial activity and strong systemicity, and has good protective and therapeutic effects on many fungal diseases caused by basidiomycetes and ascomycetes. CN201410788209.9 discloses a composite composition and fungicide containing mesifenazole and flutriafol, and specifically discloses that mesifenazole and flutriafol can be used to prevent and treat bacterial and fungal diseases, such as rice bacterial leaf streak, citrus canker, tomato bacterial wilt and peanut leaf spot. In addition, CN201310061385.8 also discloses a fungicide composition containing fluopyram, and specifically discloses that fluopyram and flutriafol have high activity against a variety of diseases on a variety of crops after compounding, and have obvious synergistic effects and expanded fungicidal spectrum.
目前还未见有粉唑醇和和多菌灵、福美双或烯肟菌胺复配的相关报道。So far, there are no reports on the combination of flutriafol and carbendazim, thiram or enoxamil.
公开于该背景技术部分的信息仅仅旨在增加对本发明的总体背景的理解,而不应当被视为承认或以任何形式暗示该信息构成已为本领域一般技术人员所公知的现有技术。The information disclosed in this background technology section is only intended to enhance the understanding of the overall background of the invention and should not be regarded as an acknowledgment or any form of suggestion that the information constitutes the prior art already known to a person skilled in the art.
发明内容Summary of the invention
本发明的目的在于提供一种含粉唑醇的杀菌组合物,其对抑制小麦赤霉病病原菌的生长表现出增效作用,可提高对小麦赤霉病的防治效果,以解决使用单一化学药剂时存在的问题。The object of the present invention is to provide a fungicide composition containing flutriafol, which has a synergistic effect on inhibiting the growth of wheat fusarium scurf disease pathogens, can improve the control effect of wheat fusarium scurf disease, and solve the problems existing when using a single chemical agent.
为实现上述目的,本发明提供了如下技术方案:To achieve the above object, the present invention provides the following technical solutions:
一种含粉唑醇的杀菌组合物,其由粉唑醇和多菌灵、福美双或烯肟菌胺复配而成。A fungicide composition containing flutriafol is prepared by compounding flutriafol with carbendazim, thiram or enoxamil.
作为优选,所述粉唑醇和多菌灵的质量比为1-40:20-1。Preferably, the mass ratio of flutriafol to carbendazim is 1-40:20-1.
作为优选,所述粉唑醇和福美双的质量比为1-10:70-1。Preferably, the mass ratio of flutriafol to thiram is 1-10:70-1.
作为优选,所述粉唑醇和福美双的质量比为1:8。Preferably, the mass ratio of flutriafol to thiram is 1:8.
作为优选,所述粉唑醇和烯肟菌胺的质量比为1-50:50-1。Preferably, the mass ratio of flutriafol to enoxadone is 1-50:50-1.
与现有技术相比,本发明具有如下有益效果:Compared with the prior art, the present invention has the following beneficial effects:
(1)本发明杀菌组合物中粉唑醇和多菌灵、福美双或烯肟菌胺的作用机理不同,在进行组合使用时,可以从不同的作用位点抑制病原菌,进而可以延缓病原菌抗性发展,延长药剂的使用寿命。(1) Flutriafol and carbendazim, thiram or enoxamyl in the fungicidal composition of the present invention have different action mechanisms. When used in combination, they can inhibit pathogens from different action sites, thereby delaying the development of pathogen resistance and extending the service life of the agent.
(2)本发明杀菌组合物对抑制小麦赤霉病病原菌表现出增效作用,可以提高对小麦赤霉病的防治效果,进而可以降低农药的施用剂量,减少防治成本。(2) The fungicidal composition of the present invention exhibits a synergistic effect on inhibiting wheat fusarium scurf pathogens, which can improve the control effect of wheat fusarium scurf, thereby reducing the application dosage of pesticides and reducing the control cost.
具体实施方式DETAILED DESCRIPTION
根据下述实施例,可以更好地理解本发明。然而,本领域的技术人员容易理解,实施例所描述的内容仅用于说明本发明,而不应当也不会限制权利要求书中所详细描述的本发明。The present invention can be better understood according to the following examples. However, it is easy for those skilled in the art to understand that the contents described in the examples are only used to illustrate the present invention, and should not and will not limit the present invention described in detail in the claims.
实施例:防治药剂筛选 Example : Screening of control agents
1.供试菌株:禾谷镰孢菌(Fusarium graminearunm),采自河南省新乡县朗公庙镇心连心实验基地内染病麦株,在实验室内分离得到,保存于PDA培养基上。1. Test strain: Fusarium graminearum, collected from diseased wheat plants in the Xinlianxin Experimental Base in Langgongmiao Town, Xinxiang County, Henan Province, isolated in the laboratory, and preserved on PDA medium.
2.供试药剂2. Test Drugs
95%粉唑醇原药、98%多菌灵原药(市售)、96%福美双原药(市售)、98%烯肟菌胺原药(市售)95% flutriafol TC, 98% carbendazim TC (commercially available), 96% thiram TC (commercially available), 98% enoxadone TC (commercially available)
将供试药剂先用二甲基亚砜溶解,再用0.1%吐温-80水溶液稀释,配制成单剂母液,设置多组配比,各单剂和配比混剂均按等比方法设置5个质量浓度梯度。The test agent was first dissolved in dimethyl sulfoxide and then diluted with 0.1% Tween-80 aqueous solution to prepare a single-dose stock solution. Multiple groups of proportions were set, and each single dose and proportioned mixture was set with 5 mass concentration gradients according to the equal ratio method.
3.试验方法3. Test methods
采用菌丝生长速率法。将预先融化的PDA培养基9mL加入无菌锥形瓶中,从低浓度到高浓度依次定量吸取药液1mL,分别加入上述锥形瓶中,充分摇匀后倒入直径为9cm的培养皿中,制成相应浓度的含药平板;并设不含药剂的处理作空白对照,每个处理设置10个重复。用直径5mm打孔器在供试菌株菌落边缘切取菌饼,接种于含药平板和空白对照平板中央,盖上皿盖后置于25℃恒温箱培养,待空白对照菌落的直径达培养皿直径的2/3以上时,,用十字交叉法测量菌落直径,计算不同处理对菌丝生长抑制率。The mycelium growth rate method was used. 9 mL of pre-melted PDA medium was added to a sterile conical flask, and 1 mL of the drug solution was quantitatively drawn from low concentration to high concentration, respectively, and added to the above conical flasks. After being fully shaken, it was poured into a culture dish with a diameter of 9 cm to make a drug-containing plate of the corresponding concentration; and a treatment without drug was set as a blank control, and 10 replicates were set for each treatment. A 5 mm diameter puncher was used to cut the bacterial cake at the edge of the test strain colony, inoculated in the center of the drug-containing plate and the blank control plate, covered with a dish cover, and placed in a 25°C constant temperature box for culture. When the diameter of the blank control colony reached more than 2/3 of the diameter of the culture dish, the colony diameter was measured using the cross method, and the mycelium growth inhibition rate of different treatments was calculated.
4.数据分析:采用DPS软件进行数据统计分析,以杀菌剂浓度对数值为x,对应的菌丝生长抑制率几率值为y进行线性回归,得出毒力回归方程及药剂对靶标病菌的毒力EC50值,并根据孙云沛法计算共毒系数(CTC)。4. Data analysis: DPS software was used for data statistical analysis. Linear regression was performed with the logarithmic value of fungicide concentration as x and the corresponding probability value of mycelium growth inhibition rate as y to obtain the toxicity regression equation and the toxicity EC50 value of the agent to the target pathogen. The co-toxicity coefficient (CTC) was calculated according to the Sun Yunpei method.
上式中:ATI--混剂实测的毒力指数;S--标准药剂的EC50,单位为mg/L;M--混剂的EC50,单位为mg/L。In the above formula: ATI - the toxicity index of the mixture measured; S - the EC 50 of the standard agent, the unit is mg/L; M - the EC 50 of the mixture, the unit is mg/L.
TTI=TIA×PA+TIB×PB TTI=TI A × PA +TI B × PB
上式中:TTI--混剂的理论毒理指数;TIA--A药剂的毒力指数;PA--A药剂在混剂中百分含量,单位为百分率(%);TIB--B药剂的毒力指数;PB--B药剂在混剂中百分含量,单位为百分率(%)。In the above formula: TTI is the theoretical toxicological index of the mixture; TI A is the toxicity index of agent A; PA is the percentage of agent A in the mixture, in percentage (%); TI B is the toxicity index of agent B; PB is the percentage of agent B in the mixture, in percentage (%).
上式中:CTC--共毒系数;ATI--混剂实测毒力指数;TTI--混剂理论毒力指数。In the above formula: CTC--co-toxicity coefficient; ATI--actual toxicity index of the mixture; TTI--theoretical toxicity index of the mixture.
5.测定结果5. Measurement results
根据计算的共毒系数(CTC)评价药剂的增效作用,CTC≤80为拮抗作用,80<CTC<120为相加作用,CTC≥120为增效作用,结果见表1-3。The synergistic effect of the drug was evaluated based on the calculated co-toxicity coefficient (CTC), CTC≤80 was antagonistic effect, 80<CTC<120 was additive effect, and CTC≥120 was synergistic effect. The results are shown in Table 1-3.
表1粉唑醇和多菌灵复配对禾谷镰孢菌的室内生物活性测定Table 1 Indoor bioactivity determination of flutriafol and carbendazim against Fusarium graminearum
由表1可知,粉唑醇和多菌灵复配后,在质量比为1-40:20-1范围内对禾谷镰孢菌的共毒系数均大于120,表现为增效作用。As shown in Table 1, after flutriafol and carbendazim were mixed, the co-toxicity coefficients against Fusarium graminearum were all greater than 120 in the mass ratio range of 1-40:20-1, showing a synergistic effect.
表2粉唑醇和福美双复配对禾谷镰孢菌的室内生物活性测定Table 2 Indoor bioactivity determination of flutriafol and thiram against Fusarium graminearum
由表2可知,粉唑醇和福美双复配后,在质量比为1-10:70-1范围内对禾谷镰孢菌的共毒系数均大于120,表现为增效作用。尤其当质量比为1:8时,共毒系数达到了608.7198,增效作用最为显著。As shown in Table 2, after flutriafol and thiram were mixed, the co-toxicity coefficient against Fusarium graminearum was greater than 120 in the mass ratio range of 1-10:70-1, showing a synergistic effect. Especially when the mass ratio was 1:8, the co-toxicity coefficient reached 608.7198, and the synergistic effect was most significant.
表3粉唑醇和烯肟菌胺复配对禾谷镰孢菌的室内生物活性测定Table 3 Indoor bioactivity determination of flutriafol and enoxamyl against Fusarium graminearum
由表3可知,粉唑醇和烯肟菌胺复配后,在质量比为1-50:50-1范围内对禾谷镰孢菌的共毒系数均大于120,表现为增效作用。As shown in Table 3, after flutriafol and enoxamyl are compounded, the co-toxicity coefficients against Fusarium graminearum are all greater than 120 in the mass ratio range of 1-50:50-1, showing a synergistic effect.
综上,本发明杀菌组合物中粉唑醇和多菌灵、福美双或烯肟菌胺复配时,对抑制小麦赤霉病病原菌表现出增效作用,可以提高对小麦赤霉病的防治效果,进而可以降低农药的施用剂量,减少防治成本。In summary, when flutriafol and carbendazim, thiram or enoxamyl are compounded in the fungicidal composition of the present invention, they show a synergistic effect in inhibiting the pathogenic bacteria of wheat fusarium scaber, which can improve the control effect of wheat fusarium scaber, thereby reducing the application dosage of pesticides and reducing the control cost.
上所述仅是本发明的优选实施方式,对于本领域技术人员来说,在不脱离本发明原理的前提下,可以做适当的改进,这些改进也在本发明的保护范围之内。The above is only a preferred embodiment of the present invention. Those skilled in the art may make appropriate improvements without departing from the principle of the present invention. These improvements are also within the protection scope of the present invention.
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