CN109221163A - 一种杀菌组合物 - Google Patents
一种杀菌组合物 Download PDFInfo
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- CN109221163A CN109221163A CN201710556960.XA CN201710556960A CN109221163A CN 109221163 A CN109221163 A CN 109221163A CN 201710556960 A CN201710556960 A CN 201710556960A CN 109221163 A CN109221163 A CN 109221163A
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- plant
- bactericidal composition
- amisulbrom
- ethyl ketone
- pyrrole ethyl
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Classifications
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- A—HUMAN NECESSITIES
- A01—AGRICULTURE; FORESTRY; ANIMAL HUSBANDRY; HUNTING; TRAPPING; FISHING
- A01N—PRESERVATION OF BODIES OF HUMANS OR ANIMALS OR PLANTS OR PARTS THEREOF; BIOCIDES, e.g. AS DISINFECTANTS, AS PESTICIDES OR AS HERBICIDES; PEST REPELLANTS OR ATTRACTANTS; PLANT GROWTH REGULATORS
- A01N43/00—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds
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Abstract
本发明提供一种杀菌组合物,所述杀菌组合物活性成分由吲唑磺菌胺和氟噻唑吡乙酮组成,其中吲唑磺菌胺和氟噻唑吡乙酮的重量百分比为50:1‑1:50。本发明还涉及所述的杀菌组合物用于控制霜霉病、晚疫病、叶斑病、纹枯病、灰霉病、白粉病、立枯病、软腐病、猝倒病的用途。本发明还涉及所述杀菌组合物施用至所需防治的地点防治土壤或栽培媒介中致病或腐生的真菌和细菌的用途。本发明还涉及所述的杀菌组合物用于处理种子以保护种子携带的植物病原菌侵袭的用途。
Description
技术领域
本发明涉及一种杀菌组合物;本发明还涉及使用所述的杀菌组合物防治有害真菌的方法。
背景技术
目前对于农业上易产生抗性的病害防治,使用作用机理不同的农药品种进行混配是最佳的选择,如果配比合理,则可以产生显著的增效作用,使田间防治效果明显优于各单剂的作用。含有单一活性成分的杀菌剂在农业病害防治上常常存在一定的缺陷,连续多次使用不但使病原菌易产生抗药性,且易造成对食品和环境的污染,通过杀菌剂活性成分之间合理混配能够克服以上缺点。合理的复配使有效成分产生的增效作用,可以提高防效,减少有效成份用量,节约成本,延缓病原菌的抗药性的产生,进而能够减轻甚至避免农药对食物和环境的污染。
关于农药活性,特别是对作物保护,该技术领域中开展的研究的核心问题之一是改善性能,尤其是生物活性方面的性能以及在一定时间内保持此活性方面的性能。
吲唑磺菌胺(Amisulbrom), 化学名为3-(3-溴-6-氟-2-甲基吲哚-1-磺酰基)-N,N-二甲基-1,2,4-三唑-1-磺酰胺,其化学结构式为:
吲唑磺菌胺化合物为日本日产化学工业株式会社开发的氨磺酰基化合物,已经在CN1158278C中公开。吲唑磺菌胺对疫病及霜霉病具有很高的杀菌活性。
氟噻唑吡乙酮(Oxathiapiprolin);CAS:1003318-67-9;化学名称为:1-(4-[4-[(5RS)-5-(2,6-二氟苯基)-4,5-二氢-1,2-噁唑-3-基]-1,3-噻唑-2-基]-1-哌啶基)-2-[5-甲基-3-(三氟甲基)-1H-吡唑-1-基]乙酮。其分子结构式为:
氟噻唑吡乙酮为杜邦开发的首个哌啶基噻唑异噁唑啉类杀菌剂,其已公开在CN101888843; 其对霜霉病和晚疫病有特效。氟噻唑吡乙酮作用位点单一,杀菌剂抗性行动委员会认为,其具有中高水平抗性风险,需要进行抗性管理。
由于现在对杀菌剂的环境要求和经济要求持续提高,例如对活性谱、毒性、选择性、施用率、残余物组成和有利的制备可行性的要求,此外还由于在例如耐药性方面可能存在问题,因此,开发在某些方面优于现有杀菌剂的新的杀菌剂是持续的任务。
发明内容
本发明提供了一种能够具有较高活性并且活性保持较久的杀菌组合物。本发明的杀菌组合物起协同增效的作用,适于防治有害真菌。
吲唑磺菌胺对某些植物有害真菌并没有发挥充分的作用,表现出治疗作用弱或持效期相对短,从而在某些应用情况下,吲唑磺菌胺表现出实际上不充分的控制作用。
另一方面,长期单一施用一种活性化合物来防治病害会导致病害抗药性产生,引起化合物防效下降,甚至彻底失去防效。为了降低植物病菌产生抗药性的风险,应用增效组合物来防治有害植物病原真菌是目前常采用的办法之一。
本发明的目的是提供一种杀菌组合物,在降低的活性化合物施用总量下就降低施用率和改善已知化合物吲唑磺菌胺和氟噻唑吡乙酮的活性谱而言,本发明在降低活性化合物施用总量下,对有害真菌具有改善活性(协同增效)。
我们已发现,同时,即联合或分开施用吲唑磺菌胺和氟噻唑吡乙酮而言,或依次施用吲唑磺菌胺和氟噻唑吡乙酮使得比单独施用各个化合物更好地防治有害真菌。
本发明提供了一种杀菌组合物,该组合物通过将吲唑磺菌胺和氟噻唑吡乙酮进行组合,使得得到的组合物在防治效果上具有增益效果,并且拓展了杀菌谱,起到了一药多用的作用,有效减缓或避免病菌产生抗药性。令人惊奇地,本发明的杀菌组合物的杀菌活性比各个活性化合物的活性的加和明显更高。换言之,存在无法预测的、真实存在的协同效应,而不仅仅是活性的增补。
当活性化合物以特定的重量比存在于本发明的杀菌组合物中时,协同效应特别明显。但是,本发明杀菌组合物中的活性化合物的重量比可在一定范围内变化。
本发明一种杀菌组合物是采取以下技术方案实现:
一种杀菌组合物,其特征在于:所述杀菌组合物含有活性成分吲唑磺菌胺和氟噻唑吡乙酮,其中吲唑磺菌胺和氟噻唑吡乙酮的重量百分比为50:1-1:50,进一步优选为40:1-1:40,再优选为30:1-1:30,更优选为25:1-1:25, 更优选为10:1-1:10,更优选5:1-1:5。
本发明中,吲唑磺菌胺和氟噻唑吡乙酮的重量百分比还可以是50:1,49:1,48:1,47:1,46:1,45:1,44:1,43:1,42:1,41:1,40:1,39:1,38:1,37:1,36:1,35:1,34:1,33:1,32:1,31:1,30:1,29:1,28:1,27:1,26:1,25:1,24:1,23:1,22:1,21:1,20:1,19:1,18:1,17:1,16:1,15:1,14:1,13:1,12:1,11:1,10:1,9:1,8:1,7:1,6:1,5:1,4:1,3:1,2:1,1:1,1:2,1:3,1:4,1:5,1:6,1:7,1:8,1:9,1:10,1:11,1:12,1:13,1:14,1:15,1:16,1:17,1:18,1:19,1:20,1:21,1:22,1:23,1:24,1:25,1:26,1:27,1:28,1:29,1:30,1:31,1:32,1:33,1:34,1:35,1:36,1:37,1:38,1:39,1:40,1:41,1:42,1:43,1:44,1:45,1:46,1:47,1:48,1:49,1:50。
一种杀菌组合物,含有活性成分吲唑磺菌胺和氟噻唑吡乙酮,还包含填充剂和/或表面活性剂。
所述的杀菌组合物, 剂型为可分散油悬浮剂、悬浮剂、种衣剂、悬乳剂、可湿性粉剂、水分散粒剂、微囊悬浮剂、包衣颗粒剂、挤出颗粒剂、乳油、微乳剂、水乳剂、泡腾片、超低容量液剂、干悬剂、静电油剂。
所述的杀菌组合物,其中吲唑磺菌胺和氟噻唑吡乙酮活性成分的含量占组合物的5%-90%,优选10%-80%,更优选20%-70%。
本发明的杀菌组合物中,吲唑磺菌胺和氟噻唑吡乙酮的质量占所述杀菌组合物以重量计的还可以例如是:
5%,6%,7%,8%,9%,10%,11%,12%,13%,14%,15%,16%,17%,18%,19%,20%,21%,22%,23%,24%,25%,26%,27%,28%,29%,30%,31%,32%,33%,34%,35%,36%,37%,38%,39%,40%,41%,42%,43%,44%,45%,46%,47%,48%,49%,50%,51%,52%,53%,54%,55%,56%,57%,58%,59%,60%,61%,62%,63%,64%,65%,66%,67%,68%,69%,70%,71%,72%,73%,74%,75%,76%,77%,78%,79%,80%,81%,82%,83%,84%,85%,86%,87%,88%,89%,90%。
一种防治植物致病菌的方法,将本发明的杀菌组合物作用于植物致病菌和/或其环境,或者植物、植物部分、植物繁殖材料和随后长出的植物器官、土壤或栽培媒介、材料或空间中。
一种防治植物致病菌的方法,将本发明所述的杀菌组合物作用于植物或植物部分。
一种防治植物致病菌的方法,将本发明所述的杀菌组合物作用于植物繁殖材料和随后长出的植物器官。
一种防治植物致病菌的方法,将本发明所述的杀菌组合物作用于土壤或栽培媒介。
一种防治植物致病菌的方法,将吲唑磺菌胺和氟噻唑吡乙酮同时施用、或分别施用、或相继施用。
一种防治植物致病菌的方法,可在植物被侵染之前或侵染之后将所述的杀菌组合物作用于植物致病菌和/或其环境,或者植物、植物部分、植物繁殖材料和随后长出的植物器官、土壤或栽培媒介、材料或空间中。
一种防治植物致病菌的方法,包括将本发明的杀菌组合物以农学有效且基本无植物毒性的施用量以种子处理、叶面施用、茎施用、浸透、滴注、浇注、喷射、喷雾、撒粉、散布或发烟等方法施用至植物致病菌和/或其环境,或者植物、植物部分、植物繁殖材料和随后长出的植物器官、土壤或栽培媒介、材料或空间中。
所述的杀菌组合物用于防治禾谷类、蔬菜、水果、观赏植物和葡萄藤上有害真菌的用途。
所述的杀菌组合物用于控制禾谷类、蔬菜、水果、观赏植物和葡萄藤上丝核菌属、轮枝孢菌属、根肿菌属、腐霉菌属、霜霉菌属、疫霉菌属、镰刀菌属、灰霉菌属、白粉菌属、毛球腔菌属、凸脐蠕孢属有害真菌的用途。
所述的杀菌组合物用于控制霜霉病、晚疫病、叶斑病、纹枯病、灰霉病、白粉病、立枯病、软腐病、大斑病、炭疽病、绿霉病、疮痂病、斑点落叶病、细菌性枯萎病、黑斑病、白娟病、猝倒病的用途。
所述的杀菌组合物用于保护植物、植物繁殖材料和随后长出的植物器官的用途。
所述的杀菌组合物施用至所需防治的地点防治土壤或栽培媒介中致病或腐生的有害真菌的用途。
所述的杀菌组合物用于处理种子以保护种子携带的植物病原菌侵袭的用途。
所述的杀菌组合物用于保护贮存物的用途。
所述的杀菌组合物用于保护贮存物在贮存期免受真菌或细菌侵染的用途。
本发明的杀菌组合物对各种植物病原菌具有很强的活性,并可对由植物病原菌引起的植物病害的预防和治疗发挥很强的防除效果。
本发明的杀菌组合物对例如担子菌纲、子囊菌纲、卵菌纲和半知菌纲等宽范围植物病原性真菌具有极好活性。
卵菌纲,包括疫霉属(Phytophthora),例如致病疫霉菌(Phytophthorainfestans)、大豆疫霉病菌(Phytophthoramegasperma)、柑桔脚腐病菌(Phytophthoraparasitica)、樟疫霉菌(Phytophthoracinnamomi)和南瓜疫病菌(Phytophthoracapsici)的病害;草腐霉枯萎属(Pythium)例如坪草腐霉枯萎病菌(Pythiumaphanidermatum)的病害;以及霜霉科(Peronosporaceae)病害例如葡萄霜霉病菌(Plasmoparaviticola)、霜霉属病菌(Peronospora)(包括烟草霜霉菌(Peronosporatabacina)和寄生霜霉菌(Peronosporaparasitica)),假霜霉属(Pseudoperonospora属)病菌(包括黄瓜霜霉病菌(Pseudoperonosporacubensis)和盘梗霉菌病菌(Bremialactucae)、腐霉属(Pythium)例如瓜果腐霉菌(Pythiumaphanidermatum);
子囊菌纲,包括链格孢属(Alternaria)病害例如番茄早疫病菌(Alternariasolani)和甘蓝黑斑病菌(Alternariabrassicae),球座菌属 (Guignardia)病害例如葡萄黑腐病菌(Guignardiabidwelli),黑星菌属(Venturia)病害例如苹果黑星病菌(Venturiainaequalis),壳针孢属(Septoria)病害例如颖枯病菌 (Septorianodorum)和叶枯病菌(Septoriatritici),白粉病例如白粉菌属(Erysiphe) (包括小麦白粉病菌(Erysiphegraminis)和萝白粉病菌(Erysiphepolygoni))、葡萄白粉病菌(Uncinulanecatur)、黄瓜白粉病菌(Sphaerothecafuligena)和苹果白粉病菌(Podosphaeraleucotricha)、小麦基腐病菌(Pseudocercosporellaherpotrichoides) 物种,灰霉菌属(Botrytis)物种病害例如草莓灰霉病菌(Botrytiscinerea)、桃褐腐病菌(Moniliniafructicola)病害,菌核菌属(Sclerotinia)物种病害例如油菜菌核病菌(Sclerotiniasclerotiorum)、稻瘟病菌(Magnaporthegrisea)、葡萄枝枯病菌(Phomopsisviticola)病害,蠕形菌属(Helminthosporium)物种病害例如玉米大斑病菌(Helminthosporiumtriticirepentis)、网纹病菌(Pyrenophorateres)物种,炭疽病害例如黑果病菌(Glomerella)或炭疽菌属(Colletotrichum属)病害(例如粱炭疽病菌(Colletotrichumgraminicola)和西瓜炭疽病菌(Colletotrichumorbiculare)),和小麦全蚀病菌(Gaeumannomycesgraminis);
担子菌纲,包括由锈菌属(Puccinia属)造成的锈菌病害(例如隐匿柄锈菌(Pucciniarecondita)、条锈菌(Pucciniastriiformis)、叶锈菌(Pucciniahordei)、杆锈菌(Pucciniagraminis)和柄锈菌(Pucciniaarachidis)),咖啡锈菌(Hemileiavastatrix)和大豆锈菌(Phakopsorapachyrhizi);
半知菌纲,包括丝核菌属(Rhizoctonia属)物种(例如立枯丝核菌(Rhizoctoniasolani)和赤色菌核病菌(Rhizoctoniaoryzae));镰刀菌属(Fusarium)病害,例如禾谷镰孢(Fusariumgraminearum),念珠镰孢菌(Fusariummoniliforme), 尖孢镰孢(Fusariumoxysporum, 串珠镰刀菌(Fusariumproliferatum), 茄病镰孢(Fusariumsolani);大丽轮枝菌(Verticilliumdahliae);白绢菌(Sclerotiumrolfsii);云纹菌(Rynchosporiumsecalis);黑涩病菌(Cercosporidiumpersonatum)、黑斑病菌(Cercosporaarachidicola)和褐斑病菌(Cercosporabeticola);银元斑病菌(Rutstroemiafloccosum)。
本发明的的杀菌组合物特别适合控制禾谷类、蔬菜、水果、观赏植物和葡萄藤上丝核菌属、轮枝孢菌属、根肿菌属、腐霉菌属、霜霉菌属、疫霉菌属、镰刀菌属、灰霉菌属、白粉菌属、毛球腔菌属、凸脐蠕孢属有害真菌的用途。
本发明的杀菌组合物特别适于控制霜霉病、晚疫病、叶斑病、纹枯病、灰霉病、白粉病、立枯病、软腐病、大斑病、炭疽病、绿霉病、疮痂病、斑点落叶病、细菌性枯萎病、黑斑病、白娟病、猝倒病的用途。
本发明的杀菌组合物适合的作物植物主要包括:谷类作物,例如小麦、大麦、燕麦、裸麦、黑小麦、水稻、玉米、高粱和小米;蔓生作物,例如鲜食葡萄和酿酒葡萄;大田作物,例如油菜(卡诺拉)、向日葵;糖用甜菜、甘蔗、大豆、花生(落花生)、烟草、苜蓿、三叶草、胡枝子、车轴草和野豌豆;仁果类水果,诸如苹果、梨、野苹果、枇杷、山楂和温柏;核果类水果,例如桃、樱桃、李子、杏、蜜桃;柑橘类水果,例如柠檬、酸橙、橙、柚子、中国柑桔(橘子)和金橘;根茎植物和大田作物(以及它们的叶子),例如洋蓟、菜用甜菜和糖用甜菜、胡萝卜、木薯、生姜、人参、山葵、欧洲防风草、马铃薯、小红萝卜、芜菁甘蓝、甘薯、芜菁和薯蓣;鳞茎植物,诸如大蒜、韭葱、洋葱和青葱;叶菜植物,例如芥子苦菜(芝麻菜)、芹菜、芹菜、水芹、菊苣(茅菜)、茴香、结球生菜和散叶莴苣、欧芹、红菊苣(红的菊苣)、大黄、菠菜和唐莴苣;芸苔属(高丽菜)叶菜,例如西兰花、花椰菜(球花甘蓝)、芽甘蓝、卷心菜、白菜、菜花、甘蓝、羽衣甘蓝、大头菜、芥菜和青菜;豆类植物(多汁的或无汁的)例如羽扇豆、菜豆)(包括蚕豆、四季豆、菜豆、花豆、红花菜豆、食荚菜豆、宽叶菜豆和黄荚种菜豆)、菜豆(包括赤豆、长豇豆、眉豆、乌豇豆、豆角、豇豆、绿豆、豇豆、黑绿豆和特长豇豆)、蚕豆、鹰嘴豆、瓜耳、刀豆、兵豆和豌豆(包括四季豆、食荚豌豆、紫花豌豆、豌豆、青豌豆、雪豆、甜豆、木豆和大豆);果菜类,诸如茄子、地樱桃、香瓜茄和辣椒(包括铃状椒、辣椒、烹调用辣椒、甘椒、甜椒;小番茄和番茄);葫芦科类蔬菜,例如佛手瓜(果实)、冬瓜、枸橼西瓜、黄瓜、嫩黄瓜、食用葫芦(包括葫芦、瓢瓜)、丝瓜、秋葵、胶苦瓜、山苦瓜、苦瓜和中国黄瓜、香瓜、西葫芦和笋瓜和西瓜;浆果类,诸如黑莓、红果莓、露莓、紫蓝莓、蓝莓、蔓越莓、黑醋栗、野莓、罗甘莓、树莓和草莓;树生坚果,例如杏仁、山毛榉坚果、巴西果、白胡桃、腰果、板栗、榛子(榛果)、山核桃、澳洲坚果、美洲山核桃和胡桃;热带水果和其他作物,例如香蕉、大蕉、芒果、椰子、木瓜、鳄梨、荔枝、龙舌兰、咖啡、可可、甘蔗、油棕、芝麻、橡胶和香料;纤维作物,例如棉花、亚麻和大麻;草皮草(包括暖季型和凉季型草皮草)。
本发明的杀菌组合物特别适用的作物植物包括水稻、黄瓜、甜瓜、卷心菜、葡萄、红椒、青椒、西瓜、南瓜、烟草、柑橘、苹果、番茄、香蕉、玉米、芦笋、苦苣、马蹄莲、花椰菜、卷心菜、魔芋、油菜、芹菜、日本萝卜、烟草、洋葱、青梗菜、番茄、茄子、胡萝卜、青洋葱、大白菜、结球甘蓝、马铃薯、生菜、油籽油菜。
本发明的杀菌组合物特别适于控制水稻植物枯萎病,水稻植物纹枯病,水稻立枯病、黄瓜炭疽病,黄瓜白粉病,黄瓜、甜瓜、巻心菜、大白菜、洋葱和葡萄的霜霉病,土豆、红椒、青椒、西瓜、南瓜、烟草和番茄的晚疫病,番茄早疫病,柑桔类水果的黑变病,柑桔类水果的普通绿霉病,梨疮痂病,苹果斑点落叶病,各种类型的灰霉病,茎腐病和锈病,白菜软腐病,玉米大斑病、香蕉叶斑病、黄瓜猝倒病。
本发明的杀菌组合物特别适于控制如下病害:
| 宿主植物 | 病害名称 | 致病生物体 |
| 马铃薯 | 马铃薯晚疫病 | 致病疫霉 |
| 黄瓜 | 黄瓜霜霉病 | 古巴假霜霉菌 |
| 香蕉 | 香蕉叶斑病 | 褐缘灰斑病 |
| 水稻 | 水稻苗期立枯病 | 禾谷镰孢菌 |
| 水稻 | 水稻纹枯病 | 立枯丝核菌 |
| 黄瓜 | 黄瓜白粉病 | 瓜类单丝壳白粉菌 |
| 番茄 | 番茄灰霉病 | 灰葡萄孢菌 |
| 白菜 | 白菜软腐病 | 胡萝卜软腐欧文氏菌 |
| 玉米 | 玉米大斑病 | 大斑凸脐蠕孢 |
| 黄瓜 | 黄瓜猝倒病 | 瓜果腐霉菌 |
本发明的杀菌组合物可以在作物保护中用作叶面杀菌剂,亦可作为杀菌剂用于拌种和用作土壤杀菌剂。
本发明的杀菌组合物可用于保护植物、植物部分、植物繁殖材料和随后长出的植物器官。
本发明的杀菌组合物用于保护植物、植物繁殖材料和随后长出的植物器官的用途。
本发明的杀菌组合物用于处理种子以保护种子携带的植物病原性真菌侵袭的用途。
本发明的杀菌组合物,可以处理所有植物和植物部分。“植物”指所有植物和植物种群,例如理想的和不理想的野生植物、栽培植物和植物品种(无论是否受植物品种或植物培育人权利的保护)。栽培植物和植物品种可以是通过常规繁殖和培育方法得到的植物,这些方法可辅以或补充有一种或多种生物技术方法,例如使用双单倍体、原生质体融合、随机和定向突变、分子或遗传标记,或使用生物工程和遗传工程方法。植物部分是指植物的所有地上和地下部分及器官,例如芽、叶、花和根,例如叶子、针叶、茎、枝、花、子实体、果实和种子以及根、球茎和根茎。作物以及营养繁殖和有性繁殖材料,例如插枝、球茎、根茎、纤匐枝和种子也属于植物部分。
一种防治植物致病菌的方法,将所述的杀菌组合物作用于植物繁殖材料和随后长出的植物器官。
术语“植物繁殖材料”应理解为指所有有繁殖能力的植物部分,例如种子,其能用于繁殖后者,以及植物性材料例如扦插条或块茎(例如马铃薯)。因此,本文中所使用的植物部分包括植物繁殖材料。可以提及的是例如种子,根,果实,块茎,鳞茎,根茎和植物部分。待从土壤中发芽后或出苗后抑制的发芽植株和有效植株。幼小植株可以在移植前通过浸渍进行全部或局部处理来进行保护。
本发明优选的植物繁殖材料是种子。本发明的杀菌组合物也特别适合处理种子。大部分的有害真菌引起的作物损害是由于在储存期间或播种之后以及在植物发芽过程中或发芽后的种子的侵害而引起的。由于生长期植物的根和枝条特别敏感并且即使小的损害也能导致植物的死亡。 本发明另一方面提供一种保护种子和发芽植物的方法,该方法使得在播种后或植物发芽后无需额外施用作物保护剂或至少显著地额外施用作物保护剂。另一方面,利用本发明的杀菌组合物优化所使用的活性化合物的量,以最大程度地提供种子和发芽植物的保护以免受植物病原性真菌的侵袭,而植物本身不会受到所使用活性化合物的损害。
因此,本发明也特别涉及通过用本发明的杀菌组合物来处理种子以保护种子和发芽植物免受植物病原性真菌侵袭的方法。本发明还涉及根据本发明的杀菌组合物在处理种子以保护种子和发芽植物免受植物病原性真菌的用途。
危害出芽后植物的植物病原性真菌的控制主要通过使用作物保护剂处理土壤和植物的地上部分来进行。考虑到作物保护剂对环境以及人和动物的健康可能产生的影响,因此有必要尽量减少活性化合物的施用量。
根据本发明的杀菌组合物适于保护在农业中、温室中、林业中或园艺-或葡萄栽培种施用的任何植物品种的种子。特别地,其采用的种子形式为谷类(如小麦、大麦、黑麦、黑小麦、稷、燕麦)、大豆、高粱、豌豆、小扁豆、玉米、棉花、大豆、水稻、马铃薯、向日葵、菜豆、咖啡、甜菜、花生、油菜、橄榄、可可、甘蔗、烟草,蔬菜(如番茄、黄瓜、洋葱和莴苣)、草坪草以及装饰用植物。谷类和蔬菜类的种子的处理是至关重要的。
本发明的杀菌组合物中的活性成分吲唑磺菌胺和氟噻唑吡乙酮单独或以适宜的制剂形式施用于种子。优选地在充分稳定的状态下处理以至于处理不会引起对种子的任何损害。通常,可在采摘和播种之间的任意时间点进行处理种子。通常所使用的种子从植物分离并且从穗轴、壳、茎、表皮、毛或果肉分离出。因此,可以使用例如,已被采摘、清洁及干燥至含水量低于15%的种子。可选择地,也可以使用干燥后例如用水处理,然后又再次干燥的种子。
种子处理的方法,例如可列举有,稀释液体或固体状的药剂或者不用稀释直接将种子浸泡在液体状态溶液中使药剂浸透种子的方法、将固体药剂或液体药剂与种子混合在一起,进行包衣处理使种子表面附着药剂的方法、在种植的同时在种子附近喷洒等方法。
植物部分和随后长出的植物器官是由植物繁殖材料例如种子产生的植物的任何部分。植物部分、植物器官和植物也可以受益于通过将杀菌组合物施用于植物繁殖材料所获得的病原菌损害保护。某些植物部分和某些场所后长出的植物器官也可以看成植物繁殖材料,其自身可以用杀菌组合物施用(或处理);从而由经处理的植物部分和经处理的植物器官产生的植物、其它的植物部分和其它的植物器官也可以受益于通过将杀菌组合物施用。
本发明的杀菌组合物施用至所需防治的地点防治土壤或栽培媒介中致病或腐生的真菌和细菌的用途。
一种防治植物致病菌的方法,将所述的杀菌组合物作用于土壤或栽培媒介。
本发明的杀菌组合物还可用于预防或控制土壤或栽培媒介里多种致病或腐生的真菌和细菌。土壤传播的真菌性病原体的实例包括链格孢属(Alternaria spp.),壳二孢属(Ascochyta spp.),灰葡萄孢(Botrytis cinerea, 尾孢属(Cercospora spp.,麦角菌(Clavicepspurpurea), 禾旋孢腔菌(Cochliobolussativus), 刺盘孢属(colletotrichumspp.,附球菌属(Epicoccum spp., 禾谷镰孢(Fusariumgraminearum),念珠镰孢菌(Fusariummoniliforme), 尖孢镰孢(Fusariumoxysporum, 串珠镰刀菌(Fusariumproliferatum), 茄病镰孢(Fusariumsolani),维胶链孢(Fusariumsubglitinans),长蠕孢属(Helminthosporiumspp),雪腐微托菌(Microdochiumnivale),青霉属(Pencilliumspp),茎点霉属(Phoma spp.),麦类核腔菌(Pyrenophoragraminea),稻瘟梨孢属(Pyriculariaoryzae),立枯丝核菌(Rhizoctoniasolani),禾谷丝核菌(Rhizoctoniacerealis),核盘菌属(Sclerotiniaspp.),壳针孢属(Septoria spp.),丝轴黑粉菌(Sphacelothecareilliana),腥黑粉菌属(Tilletia spp.),肉孢核瑚菌(Typhula incarnate),隐条黑粉菌(Urocystisocculta),黑粉菌属(Ustilago spp.),轮枝孢属(Verticillium spp.),疫霉属(Phytophthora),草腐霉枯萎属(Pythium),霜霉属(Peronospora),假霜霉属 (Pseudoperonospora)。
本发明的杀菌组合物适于控制导致土壤病害的植物病原体如镰刀霉属、丝核菌属、轮枝孢菌属和根肿菌属。
在一般情况下,土壤病菌能产生大量菌体,只要条件对病菌生长发育有利而寄主又是感病的,病菌就可以大量繁殖并能侵染寄主,在感病寄主存在下,这些病菌就可以进入持续的致病期,随着作物的连作而大量繁殖扩散,但之后养分被消耗完或土壤条件如温度、湿度等对病菌不利时,病菌又可以进入休眠期。在感病寄主不存在时,土传病菌在土壤中也能存活下来,除土壤病菌具有广泛的寄主范围外,还能在非寄主的根表面或残枝落叶上存活,与其具有腐生竞争能力是分不开的。但不同病菌是有差异的,像镰刀菌在土壤中几乎可以无限期生存下去。
本发明所述的栽培媒介是指能够使农作物生根、生长的支撑体,例如:土壤,水等,具体的原材料可以使用例如砂子、浮石、蛭石、硅藻土、琼胶、凝胶状物、高分子物质、石棉、木屑、树皮等。
向土壤中施用药剂的方法,例如将液体药剂稀释于水中或不稀释直接施用于植物体的根部或育秧用的秧田中等方法,将颗粒剂散播到植物体的根部或者育秧的秧田中的方法有在播种前将粉剂、水分散粒剂等喷洒于土壤中并与土壤整体混合的方法,播种前或栽种植物体前将粉剂、水分散粒剂稀释后喷洒于种植孔、播种沟中,在进行播种的方法等。
本发明的杀菌组合物还适用于预防或控制收获后和贮存病害。根据本发明,收获后和贮存期的疾病可以例如通过以下真菌所导致:刺盘孢属种,例如香蕉刺盘孢(Colletotrichum musae)、盘长孢状刺盘孢(Colletotrichum gloeosporioides)、辣椒刺盘孢(Colletotrichum coccodes);镰刀菌属种,例如半裸镰刀菌(Fusarium semitectum)、串珠镰刀菌(Fusarium moniliforme)、腐皮镰刀菌(Fusarium solani)、尖孢镰刀菌(Fusarium oxysporum);轮枝菌属种,例如可可轮枝孢菌(Verticillium theobromae);黑孢霉属种;葡萄孢属种,例如灰葡萄孢菌(Botrytis cinerea);地丝菌属,例如白地霉(Geotrichum candidum);拟茎点霉属种,纳塔尔拟茎点霉(Phomopsis natalensis);色二孢属种,如柑桔色二孢(Diplodia citri);链格孢属种,例如柑桔链格孢(Alternariacitri)、互隔交链孢菌(Alternaria alternata);疫霉属种,例如柑桔褐腐疫霉(Phytophthora citrophthora)、草莓疫霉(Phytophthora fragariae)、恶疫霉(Phytophthora cactorum)、烟草疫霉(Phytophthora parasitica);壳针孢属(Septoriaspp.),例如Septoria depressa;毛霉属(Mucor spp.),例如梨形毛霉 (Mucorpiriformis);链核盘菌属(Monilinia spp.),例如果生链核盘菌(Moniliniafructigena)、核果链核盘菌(Monilinia laxa);黑星菌属(Venturia spp.),例如苹果黑星菌(Venturia inaequalis)、梨黑星菌(Venturia pyrina);根霉属(Rhizopus spp.),例如匍枝根霉(Rhizopus stolonifer)、米根霉(Rhizopus oryzae);小从壳属(Glomerellaspp.),例如围小从壳(Glomerella cingulata);核盘菌属(Sclerotinia spp.),例如果生核盘菌(Sclerotinia fruiticola);长喙壳属(Ceratocystis spp.),例如奇异长喙壳(Ceratocystis paradoxa);青霉属(Penicillium spp.),例如绳状青霉 (Penicilliumfuniculosum)、扩展青霉(Penicillium expansum)、指状青霉(Penicillium digitatum)、意大利青霉(Penicillium italicum);盘长孢属(Gloeosporium spp.),例如白盘长孢(Gloeosporium album)、Gloeosporium perennans、果生盘长孢(Gloeosporiumfructigenum)、Gloeosporium singulata;壳蛇孢属(Phlyctaena spp.),如Phlyctaenavagabunda;柱孢属(Cylindrocarpon spp.),例如苹果柱孢(Cylindrocarpon mali);匍柄霉属(Stemphyllium spp.),例如黄花菜匍柄霉菌(Stemphyllium vesicarium);星裂壳孢属(Phacydiopycnis spp.),例如Phacydiopycnis malirum;根串珠霉属(Thielaviopsisspp.),例如奇异根串株霉(Thielaviopsis paradoxy);曲霉属(Aspergillus spp.),如黑曲霉(Aspergillus niger)、炭黑曲霉(Aspergillus carbonarius);丛赤壳属(Nectriaspp.),例如干癌丛赤壳菌(Nectria galligena);无柄盘菌属(Pezicula spp.)。
本发明的杀菌组合物还可用于防治果蔬贮藏期病害,并且获得了意想不到的协同增效的作用。例如由以下病原体引起的果实腐烂:
疫霉属(Phytophthora),例如致病疫霉菌 (Phytophthorainfestans)、大豆疫霉病菌(Phytophthoramegasperma)、柑桔脚腐病菌(Phytophthoraparasitica);
霜霉科(Peronosporaceae)病害例如葡萄霜霉病菌(Plasmoparaviticola)、霜霉属病菌(Peronospora);
腐霉属(Pythium)例如瓜果腐霉菌(Pythiumaphanidermatum)。
还可以在植物或植物部分生长时施用根据本发明的杀菌组合物以保护收获后的贮存物。
根据本发明的处理方法也可用于保护贮存物免受真菌和微生物的侵袭。根据本发明,将术语“贮存物”理解为是指已经源自天然生命循环且希望长期保存的植物或动物性来源的天然物质和其经加工的形式。植物来源的贮存物,例如植物或其部分,如茎、叶、块茎、种子、果实或籽粒,可以以新鲜采收的状态或以加工形式如(预)干燥、润湿、粉碎、研磨、压制或烘烤被保护。也可以是木材,粗木材形式如建筑木材、电线杆和栅栏;或成品形式,如由木材制成的家具或物品。动物来源的贮存物为兽皮、皮革、毛、毛发等。根据本发明的组合物可以防止贮存期的真菌或细菌的侵袭如腐蚀、褪色或发霉。优选将“贮存物”理解为是指植物来源的天然物质和其加工形式,更优选水果和其加工形式,如梨果、核果、无核小水果和柑橘类水果及其加工形式。
本发明提供一种控制植物、植物部分、植物繁殖材料和随后长出的植物器官的植物病原真菌的方法,该方法包括将本发明的杀菌组合物以农学有效且基本无植物毒性的施用量以种子处理、叶面施用、茎施用、浸透、滴注、浇注、喷射、喷雾、撒粉、散布或发烟等方法施用到植物、植物部分、植物繁殖材料或植物正在生长或需要在其中生长的土壤或栽培媒介中。
本发明的杀菌组合物可以通过不同的处理方法施用,这些方法例如:
-将包含所述杀菌组合物的液体喷洒到所述植物的地上部分;
-撒粉,在土壤中掺入颗粒或粉末,在所述植物周围喷洒,并在树木注射或涂抹的情况下;
-对植物的种子进行包覆或薄膜涂布。
-用于果蔬采后防腐保鲜时,通常用水稀释200-2000倍液,浸果后沥出。
本发明提供一种防治植物致病菌的方法,可以是治疗、预防或根除方法。
本发明的杀菌组合物可制成通常的药剂形态,例如乳油、可湿性粉剂、悬浮剂、液剂、颗粒剂、种衣剂等药剂形态使用,其施用量,根据有效成分的配合比例、气象条件、药剂形态、施用时期、施用方法、施用场所、防除目标有害生物、目标农作物等的不同而有差异。
一种防治植物致病菌的方法,将吲唑磺菌胺和氟噻唑吡乙酮同时施用、或分别施用、或相继施用。
一种防治植物致病菌的方法,包括将本发明的杀菌组合物以农学有效且基本无植物毒性的施用量以种子处理、叶面施用、茎施用、浸透、滴注、浇注、喷射、喷雾、撒粉、散布或发烟等方法施用到植物致病菌和/或其环境,或者植物、植物部分、植物繁殖材料和随后长出的植物器官、土壤或栽培媒介、材料或空间中。
一种防治植物致病菌的方法,将所述的杀菌组合物作用于植物或植物部分。
一种防治植物致病菌的方法,可在植物被侵染之前或侵染之后将所述的杀菌组合物作用于植物致病菌和/或其环境,或者植物、植物部分、植物繁殖材料和随后长出的植物器官、土壤或栽培媒介、材料或空间中。
根据本发明的处理可能产生超加(″协同″)效应。例如,依据本发明使用的杀菌组合物的施用率和/或拓宽其活性范围和/或增加其活性,有可能获得以下效果:更好的植物生长,对高温或低温的耐受性增加,对干旱或水或土壤盐含量的耐受性增加,开花性能提高,更容易收获,加快的成熟,更高的收获率,更大的果实,更高的植物高度,叶子的颜色更绿,开花更早,收获的产品的品质或营养价值更高,果实中糖浓度更高,收获的产品的储存稳定性和/或加工性更佳,这些益处超过了实际预估的效应。
本发明的处理方法还可用于处理繁殖材料如块茎或根茎,并且可用于处理种子、幼苗或移植(pricking out)苗以及植物或移植植物。该处理方法也可用于处理根。本发明的处理方法也可用于处理植物的地上部分如有关植物的干、茎或梗、叶子、花和果实。
-通常对于叶部处理:0.1-10000g/ha,优选10-1000g/ha,更优选10-750g/ha;对于灌溉或滴加施用而言,所述剂量甚至还可以降低,特别是当施用惰性基质如石棉或珍珠岩石时;
-对于种子处理:2-250g/100kg种子,优选3-200g/100kg种子,更优选2.5-50g/100kg种子,甚至更优选2.5-25g/100kg 种子。
-对于土壤或水面施用处理:0.1-10000g/ha,优选1-5000g/ha。
-对于果蔬采后保鲜,可稀释200-2000倍液,浸果后沥出。
上述剂量仅是一般性的示例性剂量,实际施用时本领域的技术人员会根据实际情况和需要,尤其是根据待处理的植物或作物的性质以及病菌的严重性调整施用率。
本发明的吲唑磺菌胺和氟噻唑吡乙酮组合/联合施用。包括分开、依次或同时施用吲唑磺菌胺和氟噻唑吡乙酮。优选地,所述吲唑磺菌胺和氟噻唑吡乙酮组合为包含吲唑磺菌胺和氟噻唑吡乙酮的组合物的形式。
本发明的组合物可以以制剂形式为主,即组合物中各物质已经混合,组合物的成分也可以单剂形式提供,使用前在桶或罐中混合,然后稀释至所需的浓度。其中优选以本发明提供的制剂形式为主。
作为本发明的进一步改进,本发明的杀菌组合物可配制成农业上允许的任意剂型。
作为本发明的进一步改进,本发明的杀菌组合物的剂型为气溶胶、胶囊悬浮剂、冷雾化浓缩剂、热雾化浓缩剂、胶囊粒剂、细粒剂、用于种子处理的可流动浓缩剂、即用型溶液、可喷洒粉剂、可乳化浓缩剂、水包油型乳剂、油包水型乳剂、大颗粒剂、微颗粒剂、油可分散粉末、油可混溶可流动浓缩剂、油可混溶液体、泡沫剂、糊剂、悬浮浓缩剂、可溶浓缩剂、悬浮剂、种衣剂、可湿性粉剂、水分散粒剂、可溶性粉剂、微囊悬浮剂、包衣颗粒剂、挤出颗粒剂、乳油、微乳剂、水乳剂、泡腾片、超低容量液剂、悬乳剂、超低容量冷雾化制剂、超低容量热雾化制剂。
本发明所述的杀菌组合物中,包含吲唑磺菌胺和氟噻唑吡乙酮、填充剂和/或表面活性剂。
本发明所述的杀菌组合物,其中吲唑磺菌胺和氟噻唑吡乙酮的含量占杀菌组合物的5%-90%。
所述的杀菌组合物,其中吲唑磺菌胺和氟噻唑吡乙酮的含量占杀菌组合物的10%-80%。
所述的杀菌组合物,其中吲唑磺菌胺和氟噻唑吡乙酮的含量占杀菌组合物的10%-60%。
根据本发明,术语“填充剂”指可与活性化合物相组合或联合以使其更易于施用给对象(例如植物、作物或草类)的天然或合成的有机或无机化合物。因此,所述填充剂优选为惰性的,至少应为农业可接受的。所述填充剂可以为固体或液体。
本发明中可以使用的非活性媒介既可以是固体也可以是液体的,可以作为固体媒介材料使用的有例如:植物质粉末类(例如大豆粉、淀粉、谷物粉、木粉、树皮粉、锯末、核桃壳粉、麸皮、纤维素粉末、椰壳、玉米穗轴和烟草茎的颗粒,提取植物精华后的残渣等)、纸张、锯末,粉碎合成树脂等的合成聚合体、黏土类(例如高岭土、皂土、酸性瓷土等)、滑石粉类。硅石类(例如硅藻土、硅砂、云母、含水硅酸,硅酸钙)、活性炭、天然矿物质类(浮石、绿坡缕石及沸石等)、烧制硅藻土、砂、塑料媒介等(例如聚乙烯、聚丙烯、聚偏二氯乙烯等)、氯化钾、碳酸钙、磷酸钙等的无机矿物性粉末、硫酸铵、磷酸铵、尿素、氯化铵等的化学肥料、土肥,这些物质可以单独使用或者2种以上混用。
可以作为液体媒介材料使用的可以在下列材料中选择,例如水,酒精类(例如甲醇、乙醇、异丙醇、丁醇、乙二醇等)、酮类(例如丙酮、甲基乙基酮、二异丁基甲酮、环己酮等)、醚类(例如乙醚、二恶烷、甲基纤维素、四氢呋喃等)、脂肪族碳氢化合物类(例如煤油、矿物油等)、芳香族碳氢化合物类(例如苯、甲苯、二甲苯、溶剂油、烷基萘、氯代芳烃、氯代脂肪烃、氯苯,等)、卤化碳氢化合物类、酰胺类、砜类、二甲基亚砜、矿物和植物油、动物油等。
为使有效成分化合物乳化、分散、以及/或者润湿,可以使用表面活性剂例如可以列举脂肪醇聚氧乙烯醚、聚氧乙烯烷基芳基醚、聚氧乙烯高级脂肪酸酯、聚氧乙烯醇或酚的磷酸酯、多元醇的脂肪酸酯、烷芳磺酸、萘磺酸聚合物、木质素磺酸盐、高分子梳形的支状共聚物、丁基萘磺酸盐、烷基芳基磺酸盐、烷基磺基琥珀酸钠、油脂、脂肪醇与环氧乙烷缩合物、烷基牛磺酸盐等聚丙烯酸盐、蛋白质水解物。合适的低聚糖物或聚合物,例如基于单独的乙烯单体、丙烯酸、聚氧乙烯和/或聚氧丙烯或者其与例如(多元)醇或(多元)胺的结合。
为使有效成分化合物分散稳定化、附着以及/或者结合,可使用例如黄原胶、硅酸镁铝、明胶、淀粉、纤维素甲醚、聚乙烯醇、聚乙酸乙烯酯和天然磷脂(如脑磷脂和卵磷脂)以及合成磷脂、皂土、木质素磺酸钠等辅助剂。
其中防冻剂可选用乙二醇,丙二醇,丙三醇,山梨醇。作为悬浮性产品的抗絮凝剂可以使用例如萘磺酸聚合物、聚合磷酸盐等的辅助剂。
作为消泡剂可使用有机硅消泡剂。
可以使用的着色剂,例如无机颜料,如氧化铁、氧化钛和普鲁士蓝;以及有机颜料/染料:茜素染料、偶氮染料和金属酞菁染料;以及微量元素,例如铁盐、锰盐、硼盐、铜盐、钴盐、钼盐和锌盐。
任选地,还可包含其它附加组分,例如保护胶体、粘合剂、增稠剂、触变剂、渗透剂、稳定剂、掩蔽剂。
本发明的所述制剂可通过已知方式将所述活性化合物与常规添加剂混合而制备。所述常规添加剂如常规增充剂以及溶剂或稀释剂、乳化剂、分散剂、和/或粘合剂或固定剂、润湿剂、防水剂,如果需要,还可以包含催干剂和着色剂、稳定剂、颜料、消泡剂、防腐剂、增稠剂、水以及其它加工助剂。
这些组合物不仅包括可借助合适的设备如喷雾或撒粉设备立即适用于待处理的对象,而且还包括在施用于对象之前需进行稀释的浓缩商业组合物。
本发明的含吲唑磺菌胺和氟噻唑吡乙酮还可以与其它活性成分联合施用,例如用于扩大活性谱或防止形成抗性。所述其它活性成分例如杀真菌剂、杀细菌剂、引诱剂、杀昆虫剂、杀螨剂、杀线虫剂、生长调节剂、除草剂、安全剂、肥料或化学信息素等。
本发明杀菌组合物中的活性成分也可以其本身或以其制剂形式与已知的杀真菌剂、杀细菌剂、杀螨剂、杀线虫剂或杀昆虫剂混合使用,以例如拓宽其作用谱或防止抗性的产生。
杀真菌剂:
1.核酸合成抑制剂
苯霜灵(benalaxyl)、精苯霜灵(benalaxyl-M)、磺嘧菌灵(bupirimate)、chiralaxyl、clozylacon、甲菌定(dimethirimol)、乙菌定(ethirimol)、呋氨丙灵(furalaxyl)、土菌消(hymexazole)、精甲霜灵(metalaxyl-M)、甲呋酰胺(ofurace)、噁霜灵(oxadixyl)、喹菌酮(oxolinic acid);
2.有丝分裂和细胞分裂抑制剂
苯菌灵(benomyl)、多菌灵(carbendazim)、乙霉威(diethofencarb)、麦穗宁(fuberidazole)、戊菌隆(pencycuron)、涕必灵(thiabendazole)、甲基托布津(thiophanate-methyl)、苯酰菌胺(zoxamide);
3.呼吸链抑制剂
3.1复合物I
氟嘧菌胺(diflumetorim);
3.2复合物II
啶酰菌胺(boscalid)、萎锈灵(carboxin)、甲呋酌苯胺(fenfuram)、氟酰胺(flutolanil)、呋吡唑灵(furametpyr)、丙氧灭锈胺(mepronil)、氧化萎锈灵(oxycarboxin)、吡噻菌胺(penthiopyrad)、溴氟唑菌(thifluzamide);
3.3复合物III
嘧菌酯(azoxystrobin)、氰霜唑(cyazofamid)、醚菌胺(dimoxystrobin)、enestrobin、噁唑菌酮(famoxadone)、咪唑菌酮(fenamidone)、氟嘧菌酯(fluoxastrobin)、亚胺菌(kresoxim-methyl)、叉氨苯酰胺(metominostrobin)、肟醚菌胺(orysastrobin)、吡唑醚菌酯(pyraclostrobin)、啶氧菌酯(picoxystrobin);
3.4解偶联剂
敌螨普(dinocap)、氟啶胺(fluazinam);
3.5ATP产生抑制剂
薯瘟锡(fentin acetate)、三苯锡氯(fentin chloride)、毒菌锡(fentinhydroxide)、硅噻菌胺(silthiofam);
4.氨基酸和蛋白质生物合成抑制剂
胺扑灭(andoprim)、灭瘟素(blasticidin-S)、嘧菌环胺(cyprodinil)、春雷霉素(kasugamycin)、春雷霉素一水合盐酸盐(kasugamycin hydrochloride hydrate)、嘧菌胺(mepanipyrim)、二甲嘧菌胺(pyrimethanil);
5.信号转导抑制剂
拌种咯(fenpiclonil)、氟噁菌(fludioxonil)、喹氧灵(quinoxyfen);
6.脂类和膜合成抑制剂
乙菌利(chlozolinate)、异丙定(iprodione)、杀菌利(procymidone)、烯菌酮(vinclozolin);
定菌磷(pyrazophos)、克瘟散(edifenphos)、异稻瘟净(iprobenfos)(IBP)、稻瘟灵(isoprothiolane);
7.麦角固醇生物合成抑制剂
环酰菌胺(fenhexamid) 、戊环唑(azaconazole)、双苯三唑醇(bitertanol)、糠菌唑(bromuconazole)、环唑醇(cyproconazole)、苄氯三唑醇(diclobutrazole)、苯醚甲环唑(difenoconazole)、烯唑醇(duniconazole)、烯唑醇-M(diniconazole-M)、氧唑菌(epoxiconazole)、乙环唑(etaconazole)、腈苯唑(fenbuconazole)、喹唑菌酮(fluquinconazole)、氟硅唑(flusilazole)、粉唑醇(flutriafol)、呋菌唑(furconazole)、呋醚唑(furconazole-cis)、己唑醇(hexaconazole)、酰胺唑(imibenconazole)、环戊唑醇(ipconazole)、环戊唑菌(metconazole)、腈菌唑(myclobutanil)、多效唑(paclobutrazol)、戊菌唑(penconazole)、丙环唑(propiconazole)、丙硫菌唑(prothioconazole)、硅氟唑(simeconazole)、戊唑醇(tebuconazole)、氟醚唑(tetraconazole)、三唑酮(triadimefon)、唑菌醇(triadimenol)、戊叉唑菌(triticonazole)、烯效唑(uniconazole)、伏立康唑(voriconazole)、抑霉唑(imazalil)、烯菌灵(imazalil sulphate)、恶咪唑(oxpoconazole)、异嘧菌醇(fenarimol)、呋嘧醇(flurprimidol)、氟苯嘧啶醇(nuarimol)、啶斑肟(pyrifenox)、嗪氨灵(triforine)、稻瘟酯(pefurazoate)、丙氯灵(prochloraz)、氟菌唑(triflumizole)、烯霜苯唑(viniconazole)、十二环吗啉(dodemorph)、十二环吗啉乙酸盐(dodemorph acetate)、丁苯吗啉(fenpropimorph)、克啉菌(tridemorph)、苯锈啶(fenpropidin)、螺噁茂胺(spiroxamine)、萘替芬(naftifine)、稗草畏(pyributicarb)、特比萘芬(terbinafine);
8.细胞壁合成抑制剂
苯噻菌胺(benthiavalicarb)、双丙氨膦(bialaphos)、烯酰吗啉(dimethomorph)、氟吗啉(flumorph)、缬霉威(iprovalicarb)、多抗霉素(polyoxins)、多氧霉素(polyoxorim)、有效霉素A(validamycin A);
9.黑色素生物合成抑制剂
环丙酰菌胺(capropamid)、双氯氰菌胺(diclocymet)、稻瘟酰胺(fenoxanil)、四氯苯酞(phthalide)、咯喹酮(pyroquilon);
10.抗性诱导剂
苯并噻二唑(acibenzolar-S-methyl)、噻菌灵(probenazole)、噻酰菌胺(tiadinil) ;
11.具有多位点活性的化合物
敌菌丹(captafol)、克菌丹、百菌清(chlorothalonil)、铜盐例如:克菌壮、环烷酸铜、氯氧化铜(copper oxychloride)、硫酸铜、一氧化铜、喹啉铜(oxine copper)、波尔多液、抑菌灵(dichlofluanid)、二氰蒽醌(dithianon)、多果定(dodine)、多果定游离碱(dodinefree base)、福美铁(ferbam)、氟灭菌丹(fluorofolpet)、灭菌丹(folpet)、藻菌磷(fosetyl-Al)、双胍辛盐(guazatine)、双胍辛乙酸盐(guazatine acetate)、双胍辛胺(iminoctadine)、双八胍盐(iminoctadine albesilate)、双胍辛胺乙酸盐(iminoctadinetriacetate)、代森锰铜(mancopper)、代森锰锌(mancozeb)、代森锰(maneb)、代森联(metiram)、代森联锌(metiram-zinc)、丙森锌(propineb)、硫和硫制剂包括多硫化钙、福美双(thiram)、对甲抑菌灵(tolylfluanid)、代森锌(zineb)、福美锌(ziram)
12.未知机制化合物
苯噻硫氰(benthiazole)、卡巴西霉素(capsimycin)、香芹酮(carvone)、灭螨猛(chinomethionat)、氯化苦(chloropicrin)、硫杂灵(cufraneb)、环氟菌胺(cyflufenamid)、清菌脲(cymoxanil)、棉隆(dazomet)、咪菌威(debacarb)、哒菌酮(diclomezine)、双氯酚(dichlorophen)、氯硝胺(dicloran)、野燕枯(difenzoquat)、野燕枯甲基硫酸酯(difenzoquat methyl sulphate)、二苯胺(diphenylamine)、韩乐宁(ethaboxam)、嘧菌腙(ferimzone)、氟酰菌胺(flumetover)、磺菌胺(flusulfamide)、氟啶酰菌胺(fluopicolide)、氟氯菌核利(fluoroimide)、六氯苯(hexachlorobenzene)、8-羟基喹啉、人间霉素(irumamycin)、磺菌威(methasulfocarb)、苯菌酮(metrafenone)、异硫氰酸甲酯(methyl isothiocyanate)、米多霉素(mildiomycin)、多马霉素(natamycin)、福美镍(nickeldimethyldithiocarbamate)、酞菌酯(nitrothal-isopropyl)、异噻菌酮(octhilinone)、oxamocarb、oxyfenthiin、五氯苯酚(pentachlorophenol)及其盐、2-苯基苯酚及其盐、粉病灵(piperalin)、propanosine-sodium、丙氧喹啉(proquinazid)、吡咯菌素(pyrrolnitrin)、五氯硝基苯(quintozene)、叶枯酞(tecloftalam)、四氯硝基苯(tecnazene)、唑菌嗪(triazoxide)、水杨菌胺(trichlamide)、氰菌胺(zarilamid);
杀细菌剂:
溴硝丙二醇(bronopol)、双氯酚、三氯甲基吡啶(nitrapyrin)、福镁镍(nickeldimethyldithiocarbamate)、春雷霉素、异噻菌酮(octhilinone)、羧酸呋喃(furancarboxylic acid)、土霉素(oxytetracyclin)、噻菌灵、链霉素(streptomycin)、叶枯酞、硫酸铜和其它铜制剂。
活性化合物吲唑磺菌胺和氟噻唑吡乙酮可同时施用,或分别施用,或相继施用,分开施用时的顺序对防治的结果通常无影响。
本发明的杀菌组合物可以以制剂形式为主,即组合物中各物质已经混合,组合物的成分也可以单剂形式提供,使用前在桶或罐中混合,然后稀释至所需的浓度。其中优选以本发明提供的制剂形式为主。
本发明的杀菌组合物在降低活性化合物施用总量下,对有害真菌具有改善活性(协同增效)。并且本发明的杀菌组合物对现有的杀菌剂显示出耐受性的菌也具有优异的杀菌效果。
本发明一种杀菌组合物,该组合物通过将吲唑磺菌胺和氟噻唑吡乙酮组合,使得得到的组合物在防治效果上具有增益效果,并且拓展了杀菌谱,起到了一药多用的作用,有效减缓或避免病菌产生抗药性。令人惊奇地,本发明的杀菌组合物的杀菌活性比各个活性化合物的活性的加和明显更高,存在无法预测的、真实存在的协同效应,而不仅仅是活性的增补。当活性化合物以特定的重量比存在于本发明的杀菌组合物中时,协同效应特别明显。但是,本发明杀菌组合物中的活性化合物的重量比可在一定范围内变化。
本发明杀菌组合物除了杀真菌协同效应外,还具有植物生理学效果的令人惊讶的效果。所述的植物生理学包括:
非生物胁迫抗性,包括温度抗性、耐旱性和干旱胁迫后的恢复、水利用效率(与水消耗减少相关)、洪水抗性、臭氧胁迫和UV抗性、对化学物质如重金属类、盐类、杀虫剂类(安全剂)等的抗性。
生物胁迫抗性,包括增加的真菌抗性和增加的针对线虫、病毒和细菌的抗性。
增加的植物活力,包括植物健康/植物质量和种子活力、减少的倾倒、改善的外观、增加的恢复、改善的绿化效果和改善的光合效率。
本发明提供了一种杀菌组合物,该组合物通过将吲唑磺菌胺和氟噻唑吡乙酮进行组合,使得得到的组合物在防治效果上具有增益效果,并且拓展了杀菌谱,起到了一药多用的作用,有效减缓或避免病菌产生抗药性。令人惊奇地,本发明的杀菌组合物的杀菌活性比各个活性化合物的活性的加和明显更高。换言之,存在无法预测的、真实存在的协同效应,而不仅仅是活性的增补。
具体实施方式
以下将结合实施例对本发明作进一步说明:
制剂实施例
实施例1 10%吲唑磺菌胺+10%氟噻唑吡乙酮可湿性粉剂
吲唑磺菌胺 10%
氟噻唑吡乙酮 10%
十二烷基硫酸钠6%
木质素磺酸钠5%
凹凸棒土补足至100%
将活性成分、各种助剂及填料等按配方的比例成分混合,经超细粉碎机粉碎后,即得到10%吲唑磺菌胺+10%氟噻唑吡乙酮可湿性粉剂。
实施例2 2%吲唑磺菌胺+3%氟噻唑吡乙酮乳油
吲唑磺菌胺2%
氟噻唑吡乙酮3%
乙氧基化蓖麻油5%
十二烷基苯磺酸钙 3%
N-甲基吡咯烷酮补足至100%
将上述成分按照比例配制,搅拌均匀得到均一的相。
实施例3 20%吲唑磺菌胺+10%氟噻唑吡乙酮水分散粒剂
吲唑磺菌胺 20%
氟噻唑吡乙酮10%
改性木质素磺酸钙1%
十二烷基硫酸钠 1%
尿素1%
改性凹凸棒土补足至100%
将吲唑磺菌胺、氟噻唑吡乙酮活性成分、分散剂、润湿剂、崩解剂和填料按配方的比例混合均匀,经过气流粉碎成可湿性粉剂;再加入一定量的水混合挤压造料。经干燥筛分后得到20%吲唑磺菌胺+10%氟噻唑吡乙酮水分散粒剂。
实施例4 18%吲唑磺菌胺+10%氟噻唑吡乙酮悬乳剂
油相:
氟噻唑吡乙酮10%
SOLVESSOTM200 3%
乙氧基化蓖麻油5%
水相:
吲唑磺菌胺 18%
磺化的萘磺酸-甲醛缩合产物的钠盐 1%
水补足至100%
将氟噻唑吡乙酮溶解在SOLVESSOTM200中,加入乙氧基化蓖麻油得到油相;按照配方将吲唑磺菌胺、磺化的萘磺酸-甲醛缩合产物的钠盐、水经研磨和/或高速剪切后得到吲唑磺菌胺的水悬浮剂;在搅拌下将油相加入水相得到悬乳剂。
实施例5 5%吲唑磺菌胺+ 5%氟噻唑吡乙酮包衣颗粒剂
吲唑磺菌胺5%
氟噻唑吡乙酮5%
聚乙二醇3%
高度分散的硅酸1%
碳酸钙补足至100%
在混合器中,将磨细的活性成分均匀涂布到被聚乙二醇润湿的载体上。以此方式可获得无尘包衣颗粒剂。
实施例6 5%吲唑磺菌胺+15%氟噻唑吡乙酮挤出颗粒剂
吲唑磺菌胺5%
氟噻唑吡乙酮 15%
木质素磺酸钠4%
羧甲基纤维素2%
白炭黑补足至100%
将活性组分与助剂混合并研磨,组合物用水润湿。将该组合物挤出,然后在空气流中干燥。
实施例7 10%吲唑磺菌胺+10%氟噻唑吡乙酮悬浮种衣剂
吲唑磺菌胺10%
氟噻唑吡乙酮10%
脂肪醇聚氧乙烯醚磺基琥珀酸单酯二钠5%
改性木质素磺酸钙5%
黄原胶1%
羟乙基纤维素1%
丙三醇5%
PVP-K30 1%
水补足至100%
将上述各组分按比例混合经研磨和/或高速剪切后得到种衣剂。
实施例8 20%吲唑磺菌胺+10%氟噻唑吡乙酮可分散油悬浮剂
吲唑磺菌胺20%
氟噻唑吡乙酮10%
脂肪醇聚氧乙烯醚磺基琥珀酸单酯二钠5%
改性木质素磺酸钙5%
黄原胶1%
膨润土1%
丙三醇5%
PVP-K30 1%
水 3%
大豆油补足至100%
将上述各组分按比例混合经研磨和/或高速剪切后得到可分散油悬浮剂。
实施例9 20%吲唑磺菌胺+ 10%氟噻唑吡乙酮微囊悬浮-悬浮剂
胶囊核:
氟噻唑吡乙酮 10%
Plurafac LF1312(from BASF) 3%
Emulsogen 3510 (from Clariant) 1%
胶囊壁:
Lupranat®M20S(BASF Elastogran) 3.5%
DETA (BASF SE) 1.5%
水相:
吲唑磺菌胺 20%
ATLOX ®4913 (from Croda) 4%
Synperonic PE/64 3%
黄原胶 1%
消泡剂 1%
尿素 1%
1,2-丙二醇 3%
甲基异噻唑啉酮 2%
催化剂 0.1%
水补足至 100%
将Lupranat®M20S、氟噻唑吡乙酮、Plurafac LF1312、Emulsogen 3510形成的油相加入含DETA、ATLOX ®4913的水溶液中,形成乳状液。然后加热并保温在50oC 下加入催化剂反应2小时。冷却后得到氟噻唑吡乙酮的微囊剂。
Synperonic PE/64(from Croda), 消泡剂,尿素,吲唑磺菌胺、水按比例混合均匀,并经砂磨,制备成水悬浮剂。
将含氟噻唑吡乙酮的微囊剂加入到吲唑磺菌胺的悬浮剂中,得到本发明的微囊悬浮-悬浮剂。
实施例10 20%吲唑磺菌胺+10%氟噻唑吡乙酮悬浮剂
| 吲唑磺菌胺 | 20% |
| 氟噻唑吡乙酮 | 10% |
| 甲基萘磺酸钠甲醛缩合物 | 5% |
| 二辛基琥珀酸磺酸钠 | 5% |
| 黄原胶 | 0.3% |
| 丙三醇 | 5% |
| 消泡剂 | 0.6% |
| 水 | 补足至100% |
将活性组分、分散剂、润湿剂和水等各组分按照配方的比例混合均匀,经研磨和/或高速剪切,控制粒径在5μm以下,得到20%吲唑磺菌胺+10%氟噻唑吡乙酮悬浮剂。
实施例11 1%吲唑磺菌胺+1%氟噻唑吡乙酮静电油剂
吲唑磺菌胺 1%
氟噻唑吡乙酮1%
乙氧基化蓖麻油2%
十二烷基苯磺酸钙3%
SOLVESSOTM100补足至100%
将上述各组分混合,搅拌至得到透明均一相。
实施例12 10%吲唑磺菌胺+20%氟噻唑吡乙酮水分散粒剂
吲唑磺菌胺10%
氟噻唑吡乙酮20%
改性木质素磺酸钙1%
十二烷基硫酸钠1%
硫酸铵1%
改性凹凸棒土补足至100%
将吲唑磺菌胺、氟噻唑吡乙酮活性成分、分散剂、润湿剂、崩解剂和填料按配方的比例混合均匀,经过气流粉碎成可湿性粉剂;再加入一定量的水混合挤压造料。经干燥筛分后得到10%吲唑磺菌胺+20%氟噻唑吡乙酮水分散粒剂。
实施例13 2.5%吲唑磺菌胺+2.5%氟噻唑吡乙酮水乳剂
油相:
| 吲唑磺菌胺 | 2.5% |
| 氟噻唑吡乙酮 | 2.5% |
| 油酸甲酯 | 10% |
| 聚苯乙烯 | 3.5% |
水相:
| 黄原胶 | 0.1% |
| 磺化的萘磺酸-甲醛缩合产物的钠盐 | 1% |
| 杀菌剂 | 0.2% |
| 水 | 补足至100% |
将吲唑磺菌胺和氟噻唑吡乙酮溶解在油酸甲酯中,加入聚苯乙烯得到油相;按照配方中的组分混合均匀得到水相;在搅拌下将油相加入水相得到水乳剂。
实施例14 5%吲唑磺菌胺+10%氟噻唑吡乙酮微乳剂
吲唑磺菌胺5%
氟噻唑吡乙酮10%
乙氧基化蓖麻油 10%
十二烷基苯磺酸钙 10%
SOLVESSOTM100 20%
水补足至100%
将上述各组分混合,搅拌至得到透明均一相。
实施例15 50%吲唑磺菌胺+50%氟噻唑吡乙酮
吲唑磺菌胺50%
氟噻唑吡乙酮50%
将吲唑磺菌胺、氟噻唑吡乙酮按照比例混合均匀。
实施例16 60%吲唑磺菌胺+40%氟噻唑吡乙酮
吲唑磺菌胺60%
氟噻唑吡乙酮40%
将吲唑磺菌胺、氟噻唑吡乙酮按照比例混合均匀。
实施例17 40%吲唑磺菌胺+60%氟噻唑吡乙酮
吲唑磺菌胺40%
氟噻唑吡乙酮60%
将吲唑磺菌胺、氟噻唑吡乙酮按照比例混合均匀。
以上实施例中配比为重量百分配比。
生物测试例
一、毒力测试:
依孙云沛法计算出各药剂的毒力指数及混剂的共毒系数(CTC值),当CTC ≤80,则组合物表现出拮抗作用,当80<CTC<120,则组合物表现出相加作用,当CTC ≥120,则组合物表现出增效作用。
实测毒力指数(ATI)=(标准药剂EC50/供试药剂EC50)*100
理论毒力指数(TTI)=A药剂毒力指数*混剂中A的百分含量+B药剂毒力指数*混剂中B的百分含量
共毒系数(CTC)=[混剂实测毒力指数(ATI)/混剂理论毒力指数(TTI)*100
温室毒力测试中所用的植物病原体和宿主植物
| 宿主植物 | 病害名称 | 致病生物体 |
| 马铃薯 | 马铃薯晚疫病 | 致病疫霉 |
| 黄瓜 | 黄瓜霜霉病 | 古巴假霜霉菌 |
| 香蕉 | 香蕉叶斑病 | 褐缘灰斑病 |
| 水稻 | 水稻苗期立枯病 | 禾谷镰孢菌 |
| 水稻 | 水稻纹枯病 | 立枯丝核菌 |
| 黄瓜 | 黄瓜白粉病 | 瓜类单丝壳白粉菌 |
| 番茄 | 番茄灰霉病 | 灰葡萄孢菌 |
| 白菜 | 白菜软腐病 | 胡萝卜软腐欧文氏菌 |
| 玉米 | 玉米大斑病 | 大斑凸脐蠕孢 |
| 黄瓜 | 黄瓜猝倒病 | 瓜果腐霉菌 |
试验一:致病疫霉菌的毒力测定
采用抑制菌丝生长速率法:
将吲唑磺菌胺和氟噻唑吡乙酮分别用丙酮溶解,再用0.1%的吐温-80 水溶液稀释配制成系列浓度的药液,在超净工作台中分别吸取6mL到灭菌的三角烧瓶,加入50℃左右的马铃薯葡萄糖琼脂培养基(PDA)54mL,摇匀后倒入4个直径9cm的平皿,制成4个相应浓度的含毒培养基;用同样的方法将不同配比的吲唑磺菌胺和氟噻唑吡乙酮系列浓度复配药液制成含毒培养基。将培养2天的致病疫霉菌,用直径5mm的打孔器在菌落边缘打成菌块,用接种针将菌块移至预先配制成的含毒PDA培养基中央,然后置于25℃培养箱内培养,每处理重复4次。3天后,采用十字交叉法用卡尺量取各处理菌落直径cm,求出校正抑制百分率。每个菌落十字交叉测两个直径,以其平均数代表菌落大小。然后按下式求出菌落生长抑制率:
然后用最小二乘法计算抑制中浓度EC50,再依孙云沛法计算共毒系数(CTC)。
表1:对致病疫霉菌的毒力测试结果
从表1可知,吲唑磺菌胺和氟噻唑吡乙酮的组合在配比50:1-1:50的范围里时,对致病疫霉菌共毒系数均大于120,表现为协同增效的效果。
试验二:古巴假霜霉菌的毒力测定
采用抑制菌丝生长速率法:
将吲唑磺菌胺和氟噻唑吡乙酮分别用丙酮溶解,再用0.1%的吐温-80 水溶液稀释配制成系列浓度的药液,在超净工作台中分别吸取6mL到灭菌的三角烧瓶,加入50℃左右的马铃薯葡萄糖琼脂培养基(PDA)54mL,摇匀后倒入4个直径9cm的平皿,制成4个相应浓度的含毒培养基;用同样的方法将不同配比的吲唑磺菌胺和氟噻唑吡乙酮系列浓度复配药液制成含毒培养基。将培养2天的古巴假霜霉菌,用直径5mm的打孔器在菌落边缘打成菌块,用接种针将菌块移至预先配制成的含毒PDA培养基中央,然后置于25℃培养箱内培养,每处理重复4次。3天后,采用十字交叉法用卡尺量取各处理菌落直径cm,求出校正抑制百分率。每个菌落十字交叉测两个直径,以其平均数代表菌落大小。然后按下式求出菌落生长抑制率:
然后用最小二乘法计算抑制中浓度EC50,再依孙云沛法计算共毒系数(CTC)。
表2:对古巴假霜霉菌的毒力测试结果
从表2可知,吲唑磺菌胺和氟噻唑吡乙酮的组合在配比50:1-1:50的范围里时,对古巴假霜霉菌共毒系数均大于120,表现为协同增效的效果。
实验三:吲唑磺菌胺和氟噻唑吡乙酮对褐缘灰斑病菌的室内毒力测定
采用抑制菌丝生长速率法:
将吲唑磺菌胺和氟噻唑吡乙酮分别用丙酮溶解,再用0.1%的吐温-80 水溶液稀释配制成系列浓度的药液,在超净工作台中分别吸取6mL到灭菌的三角烧瓶,加入50℃左右的马铃薯葡萄糖琼脂培养基(PDA)54mL,摇匀后倒入4个直径9cm的平皿,制成4个相应浓度的含毒培养基;用同样的方法将不同配比的吲唑磺菌胺和氟噻唑吡乙酮系列浓度复配药液制成含毒培养基。将培养2天的褐缘灰斑病菌,用直径5mm的打孔器在菌落边缘打成菌块,用接种针将菌块移至预先配制成的含毒PDA培养基中央,然后置于25℃培养箱内培养,每处理重复4次。3天后,采用十字交叉法用卡尺量取各处理菌落直径cm,求出校正抑制百分率。每个菌落十字交叉测两个直径,以其平均数代表菌落大小。然后按下式求出菌落生长抑制率:
然后用最小二乘法计算抑制中浓度EC50,再依孙云沛法计算共毒系数(CTC)。
表3:对褐缘灰斑病菌的毒力测试结果
从表3可知,吲唑磺菌胺和氟噻唑吡乙酮的组合在配比50:1-1:50的范围里时,对褐缘灰斑病菌共毒系数均大于120,表现为协同增效的效果。
实验四:吲唑磺菌胺和氟噻唑吡乙酮对禾谷镰刀菌的室内毒力测定
采用抑制菌丝生长速率法:
将吲唑磺菌胺和氟噻唑吡乙酮分别用丙酮溶解,再用0.1%的吐温-80 水溶液稀释配制成系列浓度的药液,在超净工作台中分别吸取6mL到灭菌的三角烧瓶,加入50℃左右的马铃薯葡萄糖琼脂培养基(PDA)54mL,摇匀后倒入4个直径9cm的平皿,制成4个相应浓度的含毒培养基;用同样的方法将不同配比的吲唑磺菌胺和氟噻唑吡乙酮系列浓度复配药液制成含毒培养基。将培养2天的禾谷镰刀菌,用直径5mm的打孔器在菌落边缘打成菌块,用接种针将菌块移至预先配制成的含毒PDA培养基中央,然后置于25℃培养箱内培养,每处理重复4次。3天后,采用十字交叉法用卡尺量取各处理菌落直径cm,求出校正抑制百分率。每个菌落十字交叉测两个直径,以其平均数代表菌落大小。然后按下式求出菌落生长抑制率:
然后用最小二乘法计算抑制中浓度EC50,再依孙云沛法计算共毒系数(CTC)。
表4:对禾谷镰刀菌的毒力测试结果
从表4可知,吲唑磺菌胺和氟噻唑吡乙酮的组合在配比50:1-1:50的范围里时,对禾谷镰刀菌共毒系数均大于120,表现为协同增效的效果。
实验五:吲唑磺菌胺和氟噻唑吡乙酮对立枯丝核菌的室内毒力测定
采用抑制菌丝生长速率法:
将吲唑磺菌胺和氟噻唑吡乙酮分别用丙酮溶解,再用0.1%的吐温-80 水溶液稀释配制成系列浓度的药液,在超净工作台中分别吸取6mL到灭菌的三角烧瓶,加入50℃左右的马铃薯葡萄糖琼脂培养基(PDA)54mL,摇匀后倒入4个直径9cm的平皿,制成4个相应浓度的含毒培养基;用同样的方法将不同配比的吲唑磺菌胺和氟噻唑吡乙酮系列浓度复配药液制成含毒培养基。将培养2天的立枯丝核菌,用直径5mm的打孔器在菌落边缘打成菌块,用接种针将菌块移至预先配制成的含毒PDA培养基中央,然后置于25℃培养箱内培养,每处理重复4次。3天后,采用十字交叉法用卡尺量取各处理菌落直径cm,求出校正抑制百分率。每个菌落十字交叉测两个直径,以其平均数代表菌落大小。然后按下式求出菌落生长抑制率:
然后用最小二乘法计算抑制中浓度EC50,再依孙云沛法计算共毒系数(CTC)。
表5:对立枯丝核菌的毒力测试结果
从表5可知,吲唑磺菌胺和氟噻唑吡乙酮的组合在配比50:1-1:50的范围里时,对立枯丝核菌共毒系数均大于120,表现为协同增效的效果。
实验六:吲唑磺菌胺和氟噻唑吡乙酮对瓜类单丝壳白粉菌的室内毒力测定
采用抑制菌丝生长速率法:
将吲唑磺菌胺和氟噻唑吡乙酮分别用丙酮溶解,再用0.1%的吐温-80 水溶液稀释配制成系列浓度的药液,在超净工作台中分别吸取6mL到灭菌的三角烧瓶,加入50℃左右的马铃薯葡萄糖琼脂培养基(PDA)54mL,摇匀后倒入4个直径9cm的平皿,制成4个相应浓度的含毒培养基;用同样的方法将不同配比的吲唑磺菌胺和氟噻唑吡乙酮系列浓度复配药液制成含毒培养基。将培养2天的瓜类单丝壳白粉菌,用直径5mm的打孔器在菌落边缘打成菌块,用接种针将菌块移至预先配制成的含毒PDA培养基中央,然后置于25℃培养箱内培养,每处理重复4次。3天后,采用十字交叉法用卡尺量取各处理菌落直径cm,求出校正抑制百分率。每个菌落十字交叉测两个直径,以其平均数代表菌落大小。然后按下式求出菌落生长抑制率:
然后用最小二乘法计算抑制中浓度EC50,再依孙云沛法计算共毒系数(CTC)。
表6:对瓜类单丝壳白粉菌的毒力测试结果
从表6可知,吲唑磺菌胺和氟噻唑吡乙酮的组合在配比50:1-1:50的范围里时,对瓜类单丝壳白粉菌共毒系数均大于120,表现为协同增效的效果。
实验七:吲唑磺菌胺和氟噻唑吡乙酮对灰葡萄孢菌的室内毒力测定
采用抑制菌丝生长速率法:
将吲唑磺菌胺和氟噻唑吡乙酮分别用丙酮溶解,再用0.1%的吐温-80 水溶液稀释配制成系列浓度的药液,在超净工作台中分别吸取6mL到灭菌的三角烧瓶,加入50℃左右的马铃薯葡萄糖琼脂培养基(PDA)54mL,摇匀后倒入4个直径9cm的平皿,制成4个相应浓度的含毒培养基;用同样的方法将不同配比的吲唑磺菌胺和氟噻唑吡乙酮系列浓度复配药液制成含毒培养基。将培养2天的灰葡萄孢菌,用直径5mm的打孔器在菌落边缘打成菌块,用接种针将菌块移至预先配制成的含毒PDA培养基中央,然后置于25℃培养箱内培养,每处理重复4次。3天后,采用十字交叉法用卡尺量取各处理菌落直径cm,求出校正抑制百分率。每个菌落十字交叉测两个直径,以其平均数代表菌落大小。然后按下式求出菌落生长抑制率:
然后用最小二乘法计算抑制中浓度EC50,再依孙云沛法计算共毒系数(CTC)。
表7:对灰葡萄孢菌的毒力测试结果
从表7可知,吲唑磺菌胺和氟噻唑吡乙酮的组合在配比50:1-1:50的范围里时,对灰葡萄孢菌共毒系数均大于120,表现为协同增效的效果。
实验八:吲唑磺菌胺和氟噻唑吡乙酮对大斑凸脐蠕孢菌的室内毒力测定
采用抑制菌丝生长速率法:
将吲唑磺菌胺和氟噻唑吡乙酮分别用丙酮溶解,再用0.1%的吐温-80 水溶液稀释配制成系列浓度的药液,在超净工作台中分别吸取6mL到灭菌的三角烧瓶,加入50℃左右的马铃薯葡萄糖琼脂培养基(PDA)54mL,摇匀后倒入4个直径9cm的平皿,制成4个相应浓度的含毒培养基;用同样的方法将不同配比的吲唑磺菌胺和氟噻唑吡乙酮系列浓度复配药液制成含毒培养基。将培养2天的大斑凸脐蠕孢菌,用直径5mm的打孔器在菌落边缘打成菌块,用接种针将菌块移至预先配制成的含毒PDA培养基中央,然后置于25℃培养箱内培养,每处理重复4次。3天后,采用十字交叉法用卡尺量取各处理菌落直径cm,求出校正抑制百分率。每个菌落十字交叉测两个直径,以其平均数代表菌落大小。然后按下式求出菌落生长抑制率:
然后用最小二乘法计算抑制中浓度EC50,再依孙云沛法计算共毒系数(CTC)。
表8:对大斑凸脐蠕孢菌的毒力测试结果
从表8可知,吲唑磺菌胺和氟噻唑吡乙酮的组合在配比50:1-1:50的范围里时,对大斑凸脐蠕孢菌共毒系数均大于120,表现为协同增效的效果。
实验九:吲唑磺菌胺和氟噻唑吡乙酮对胡萝卜软腐欧文氏菌的室内毒力测定
采用抑制菌丝生长速率法:
将吲唑磺菌胺和氟噻唑吡乙酮分别用丙酮溶解,再用0.1%的吐温-80 水溶液稀释配制成系列浓度的药液,在超净工作台中分别吸取6mL到灭菌的三角烧瓶,加入50℃左右的马铃薯葡萄糖琼脂培养基(PDA)54mL,摇匀后倒入4个直径9cm的平皿,制成4个相应浓度的含毒培养基;用同样的方法将不同配比的吲唑磺菌胺和氟噻唑吡乙酮系列浓度复配药液制成含毒培养基。将培养2天的胡萝卜软腐欧文氏菌,用直径5mm的打孔器在菌落边缘打成菌块,用接种针将菌块移至预先配制成的含毒PDA培养基中央,然后置于25℃培养箱内培养,每处理重复4次。3天后,采用十字交叉法用卡尺量取各处理菌落直径cm,求出校正抑制百分率。每个菌落十字交叉测两个直径,以其平均数代表菌落大小。然后按下式求出菌落生长抑制率:
然后用最小二乘法计算抑制中浓度EC50,再依孙云沛法计算共毒系数(CTC)。
表9:对胡萝卜软腐欧文氏菌的毒力测试结果
从表9可知,吲唑磺菌胺和氟噻唑吡乙酮的组合在配比50:1-1:50的范围里时,对胡萝卜软腐欧文氏菌共毒系数均大于120,表现为协同增效的效果。
实验十:吲唑磺菌胺和氟噻唑吡乙酮对瓜果腐霉菌的室内毒力测定
采用抑制菌丝生长速率法:
将吲唑磺菌胺和氟噻唑吡乙酮分别用丙酮溶解,再用0.1%的吐温-80 水溶液稀释配制成系列浓度的药液,在超净工作台中分别吸取6mL到灭菌的三角烧瓶,加入50℃左右的马铃薯葡萄糖琼脂培养基(PDA)54mL,摇匀后倒入4个直径9cm的平皿,制成4个相应浓度的含毒培养基;用同样的方法将不同配比的吲唑磺菌胺和氟噻唑吡乙酮系列浓度复配药液制成含毒培养基。将培养2天的瓜果腐霉菌,用直径5mm的打孔器在菌落边缘打成菌块,用接种针将菌块移至预先配制成的含毒PDA培养基中央,然后置于25℃培养箱内培养,每处理重复4次。3天后,采用十字交叉法用卡尺量取各处理菌落直径cm,求出校正抑制百分率。每个菌落十字交叉测两个直径,以其平均数代表菌落大小。然后按下式求出菌落生长抑制率:
然后用最小二乘法计算抑制中浓度EC50,再依孙云沛法计算共毒系数(CTC)。
表10:对瓜果腐霉菌的毒力测试结果
从表10可知,吲唑磺菌胺和氟噻唑吡乙酮的组合在配比50:1-1:50的范围里时,对瓜果腐霉菌共毒系数均大于120,表现为协同增效的效果。
Claims (16)
1.一种杀菌组合物,其特征在于:所述杀菌组合物含有活性成分吲唑磺菌胺和氟噻唑吡乙酮,其中吲唑磺菌胺和氟噻唑吡乙酮的重量百分比为50:1-1:50,进一步优选为40:1-1:40,再优选为30:1-1:30,更优选为25:1-1:25, 更优选为10:1-1:10,更优选5:1-1:5。
2.根据权利要求1所述的杀菌组合物,其特征在于:所述吲唑磺菌胺和氟噻唑吡乙酮质量之和占所述杀菌组合物质量的5%-90%,优选10%-80%,更优选20%-70%。
3.根据权利要求1所述的杀菌组合物,其特征在于:所述杀菌组合物,其剂型为悬浮剂、种衣剂、悬乳剂、可湿性粉剂、水分散粒剂、微囊悬浮剂、包衣颗粒剂、挤出颗粒剂、乳油、微乳剂、水乳剂、泡腾片、超低容量液剂、干悬剂、静电油剂。
4.根据权利要求1所述的杀菌组合物,其特征在于:还包含填充剂和/或表面活性剂。
5.一种防治植物致病菌的方法,其特征在于:将权利要求1所述的杀菌组合物作用于植物致病菌和/或其环境,或者植物、植物部分、植物繁殖材料和随后长出的植物器官、土壤或栽培媒介、材料或空间中。
6.一种防治植物致病菌的方法,其特征在于:将权利要求1所述的吲唑磺菌胺和氟噻唑吡乙酮同时施用、或分别施用、或相继施用。
7.一种防治植物致病菌的方法,其特征在于:在植物被侵染之前或侵染之后将权利要求1所述的杀菌组合物作用于植物致病菌和/或其环境,或者植物、植物部分、植物繁殖材料和随后长出的植物器官、土壤或栽培媒介、材料或空间中。
8.一种防治植物致病菌的方法,其特征在于:包括将权利要求1所述的杀菌组合物以农学有效且基本无植物毒性的施用量以种子处理、叶面施用、茎施用、浸透、滴注、浇注、喷射、喷雾、撒粉、散布或发烟等方法施用至植物致病菌和/或其环境,或者植物、植物部分、植物繁殖材料和随后长出的植物器官、土壤或栽培媒介、材料或空间中。
9.权利要求1所述的杀菌组合物用于防治禾谷类、蔬菜、水果、观赏植物和葡萄藤上真菌和细菌的用途。
10.权利要求1所述的杀菌组合物用于控制禾谷类、蔬菜、水果、观赏植物和葡萄藤上丝核菌属、轮枝孢菌属、根肿菌属、腐霉菌属、霜霉菌属、疫霉菌属、镰刀菌属、灰霉菌属、白粉菌属、毛球腔菌属、凸脐蠕孢属有害真菌的用途。
11.权利要求1所述的杀菌组合物用于控制霜霉病、晚疫病、叶斑病、纹枯病、灰霉病、白粉病、立枯病、软腐病、大斑病、炭疽病、绿霉病、疮痂病、斑点落叶病、细菌性枯萎病、黑斑病、白娟病、猝倒病的用途。
12.权利要求1所述的杀菌组合物用于保护植物、植物繁殖材料和随后长出的植物器官的用途。
13.权利要求1所述的杀菌组合物施用至所需防治的地点防治土壤或栽培媒介中致病或腐生的真菌和细菌的用途。
14.权利要求1所述的杀菌组合物用于处理种子以保护种子携带的植物病原菌侵袭的用途。
15.权利要求1所述的杀菌组合物用于保护贮存物的用途。
16.权利要求1所述的杀菌组合物用于保护贮存物在贮存期免受真菌或细菌侵染的用途。
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