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山东省烟草野火病的调查鉴定及其综合防治技术的研究
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摘要
烟草野火病是烟草上的重要细菌性病害之一。世界各主产烟区均普遍发生,以美国、德国等发病较重,甚至是毁灭性的。国内自二十世纪八十年代中期以来各主产烟区频繁发生,局部烟区呈暴发现象,以黑龙江、辽宁、云南等省区发生面积大、危害重。近年来烟草野火病在山东主产烟区频繁发生,局部烟区呈爆发现象,已经成为烟叶稳产优质的重要影响因素之一。为明确病害的发生、分布及危害情况,鉴定明确及其生理生化、生物学特性、发生规律,研究有效的防治方法,于2004~2007年对山东主产烟区烟草野火病的发生、分布及危害、发病规律及其综合防治技术等进行了较系统研究,获得结果如下:
     1.调查明确了山东省烟草野火病的发生范围已达临沂、潍坊、日照、淄博、青岛等5个主要生产烟区的18个县(市),分别为沂水、沂南、临沐、费县、平邑、蒙阴、诸城、安丘、临朐、昌乐、潍城区、东港区、莒县、沂源、临淄、博山和胶南等县(市)区。
     2.鉴定明确了山东省烟草野火病菌为假单胞杆菌属,丁香假单胞菌烟草变种Pseudomonas syringae pv.tabaci[Wolf & Foster(1917)Young,Dye & Wilkie(1978)]。
     3.室内人工接种测定明确了烟草野火病菌可侵染烟草(NC82)、心叶烟、辣椒、番茄、菜豆、蔓陀萝和龙葵等7种植物。
     4.调查明确山东烟区野火病每年有两次明显的发病高峰。第一次发生在6月中下旬,第二次发生在7月下旬至8月上旬。
     5.室内接种测定明确了45个烟草品种对野火病的抗病性,根据品种抗病程度,表现高抗的有白肋21和G80,病情指数为12.5,仅占供试总品种的4.44%;表现抗病的品种有NC89、白肋37、小黄金1025等,占总品种的31.1%;K326、红花大金元等表现感病,占35.6%;高感品种有云烟85、G28等,病情指数都在70以上,占供试总品种的28.9%。
     6.室内药剂测定筛选、组合复配、田间小区试验,选择出对野火病具有良好防治效果的铜高尚+新植霉素药剂组合。
     7.研究组合成“以种植抗病品种和药剂防治相结合的综合防治技术”,分别在沂水、沂南等县病区进行了田间多点综合防治应用。在沂水、沂南两个县平均防效分别达80.5%和78.4%,有效控制了野火病的危害。
Wildfire disease of tobacco is one of the important bacterial diseases on tobacco. The main product cigarettes areas happened commonly with morbidity serious in the world,such as USA and Germany,even is fatal.Every host product cigarette area frequently happens in the homeland since twenty centuries eighties medium term,part cigarette area presents to phenomenon break out,some province area sarea happened heavy such as Heilongjiang,Liaoning,Yunnan and so on..The tobacco wild fire disease frequently happens in recent years in Shandong host product cigarette area,part cigarette area assumes the outburst phenomenon,what has becoming one of affect factors in tobacco leaf dependable crop high grade.For definituding occurrence,distribution and damage condition,making disease clear,identify clear and definite their physiology biochemistry,Biology characteristic,rule happened,method studying effective control technology research,author carried out the studies of occurrence,distribution and damage,morbidity rule and their integrated control technology producing the cigarette area tobacco wild fire disease in 2004 to 2007 in Shandong host.The result having gained as follows:
     1.On inquiry clear and definite the range of Shandong Province tobacco wild fire disease happened already have reached 18 county(city),as follows LinYi City,Wei Fang City,RiZhao,ZiBo City,Qingdao and so on 5 main product cigarette area.such as YiShui county,YiNan county,LinMu,Fei county,PingYi county,Meng Yin county,ZhuCheng City,AnQiu,LinQu county,ChangLe county,WeiCheng Qu,Dong Gang District,Ju county,JiaoNan City,YiYuan county,LinZi,BoShan district and JiaoNan City and so on county(city) area.
     2.The appraisal has made clear that Shandong Province tobacco wild fire germs is Pseudomonas svringae pv.tabaci[Wolf & Foster(1917) Youngs,Dye & Wilkie(1978)].
     3.The indoor inoculation determining clear tobacco wild fire germs having invaded 7 kinds plant such as tobacco(NC82),heart leaf cigarette,capsicum,tomato,kidney bean,tendrilled vine lump trailing plants and black nightshade.
     4.Make clear that the Shandong cigarette area wild fire disease has twice the obvious morbidity peak every year on inquiry.In happening for the first time on June,the last ten-day period of a month,second time happen in the last ten-day period of a month in July till the first ten-day period of a month in August.
     5.The indoor inoculation determining clear disease resistance of 45 tobacco cultivars on P.s.pv.tabaci were identified,the result indicated that each cultivar was different form others.Burley 21 and G80,whose disease index were 12.5,were the two most resistant of all cultivars;Resistant cultivars including Burley 37 and Xiao huangjin 1025 et al took 31.1%of total tested cultivars;Susceptible cultivars,such as K326, Honghuadajinyuan and so on,took 35.6%;Highly suscepible cultivars including Yunyan 85,G28 et al,whose disease index were more than 70%,and they took 28.9%of all tested cultivars.
     6.The interior medicament admeasurement filtration,combination matches for again,field state tests,choosing fine copper of control technology effect to wild fire disease is medicament combination,noblenessthe copper + the newly plant mildew element in the field.
     7.Study combination "cultivate integrated control technology of integration of disease-resistant breed with medicament prevention and cure",the integrated control having carried out the field multiple;spot respectively applies to county disease area such as Yi Shui county,Yi Nan county.Two counties guard against an effect averagely in Yi Shui county,Yi Nan county amounting to 80.5%and 78.4%respectively,have an effect to hay controlled result on wild fire disease damage.
引文
1.白宝璋,朱广发,谭桂茹等.烟草叶片感染野火病时的某些生理生化变化.吉林农业大学学报,1994,16(2):28-30.
    2.常乃滔,薛应龙.T-2毒素对小麦叶片原生质体活力影响.科学通报,1989,(7):537-539.
    3.陈建中,盛炳成,刘克钧.苹果感染轮纹病菌后过氧化物酶和多酚氧化酶活性的变化.江苏农业学报,1997,13(1):63-64.
    4.陈捷等.玉米茎腐病菌致病因子的初步研究.植物病理学报,1995,25(1):77.
    5.陈捷等.玉米茎腐病菌毒素研究(Ⅱ).玉米科学(增刊),1995,36-46.
    6.陈利峰,宋玉立,徐雍皋等.抗感赤霉病小麦品种超氧化物歧化酶和过氧化氢酶的活性比较.植物病理学报,1997,27(3):209-213.
    7.陈瑞泰,王智发,王念慈.烟草病虫害防治脐南:山东科学技术出版社.1989.
    8.C.S.霍尔敦等.俞大绂等译.植物病理学-问题与进展.北京:科学出版社.1963.
    9.董汉松,王智发,曲建军.烟草对赤星病菌毒素的快速反应及其在品种抗性鉴定中的作用.中国烟草学会第二次会员代表大会会刊,1992:74-79.
    10.董金皋,李树正.植物病原菌毒素研究进展(第一卷).中国科学技术出版社,1997.
    11.董金皋,史有艳,黄梧芳.玉米大斑病菌Ht毒素的萃取及其致病活性.微生物学通报,1993,20(2):73-77.
    12.董金皋,朱希.真菌毒素生物测定方法研究概况Ⅰ植株和组织器官水平的生物测定.河北农业大学学报,1992,15(4):99-103.
    13.方中达.植病研究方法(第三版)[M].中国农业出版社.1998,179-210.
    14.高必达.烟草野火病菌毒素的分子生物学研究进展.生物技术通报,1999,(5):23-25.
    15.高必达,吴友三.麦根长蠕孢毒素的研究概况.沈阳农业大学学报,1991,22(2):158.
    16.高洁等.烟草野火病发病规律的研究.吉林农业大学学报,1997,19(1):8-15.
    17.葛莘.烟草假单胞杆菌(Pseudomonas syringae pv.tabaci)菌落的扫描电镜和微分干涉差显微镜观察.东北农学院学报,1988,19(4):354-359.
    18.葛莘,王吉长.烟草野火病原细菌(Pseudomonas syringae pv.tabaci)的鉴定.东北农学院学报,1987,18(4):311-316.
    19.葛秀春,宋凤鸣,郑重.稻瘟菌侵染后水稻幼苗活性氧的产生与抗病性的关系.植物生理学报.2000,26(3):227-231.
    20.H.惠勒.沈崇尧译.植物病程.北京:科学出版社.1979.
    21.孔凡玉.我国烟草侵染性病害发生趋势、原因及防治对策.中国烟草,1995,(1):23-25.
    22.李宝聚,李凤云.黄瓜抗黑星病品种表皮结构和若干酶系活性的研究.园艺学报,1999,26(3):198-200.
    23.李静,黄梧芳.应用组织培养法诱发小麦抗赤霉素突变研究初报.河北农业大学学报,1992,15(1):47-51.
    24.李靖,利容千,袁文静.黄瓜感染霜酶病菌叶片中一些酶活性的变化.植物病理学报,1991,21(4):277-282.
    25.李兰真,赵会杰,杨会武等.小麦锈病与活性氧代谢的关系.植物生理学报,1999,35(2):115-117.
    26.李秀琴,陈捷等.玉米全蚀病菌毒素的初步研究.沈阳农业大学学报,1992,23(3):221-223.
    27.铃木直治等,张际中等译.近代植物病理化学.上海教育出版社.1981.
    28.刘正坪,王若菁,张富荣等.茄子黄萎病菌毒素对茄种子发芽及幼苗生长的毒害作用.华北农学报,2001,16(1):63-66.
    29.罗广华,王爱国.植物SOD的凝胶电泳及活性的显示.植物生理学通讯,1983,(6):44-45.
    30.欧阳光察.稻瘟病菌(Pyricularia oryzae)毒素对水稻抗病性的诱导与苯丙烷类代谢途径的关系.植物生理学通讯,1987,(4):40.
    31.邵金旺,党俊梅,张家骅等.甜菜抗(耐)丛根病生理基础的研究(Ⅰ).内蒙古农业大学学报,1999,20(4):1-6.
    32.沈其益,阎隆飞,李庆基等.棉花感染枯萎病菌后过氧化物酶同工酶的变化.植物学报,1978,20(2):108-112.
    33.宋纪真,李忠信.烟草野火病发病规律初探.烟草科技,1989,(6):32-33.
    34.宋凤鸣,郑重,葛秀春.活性氧及膜质过氧化在植物-病原物互作中的作用.植物生理通讯,1996,32(5):377-385.
    35.谈文.烟草病理学教程.北京:中国科学技术出版社,1995.149-153.
    36.王金陵,许文耀.稻瘟病菌毒素的制备及其对水稻毒性测定.福建农学院学报,1988,17(4):318-322.
    37.王金生.植物抗病性研究进展.植物病理学报,1995,25(4):289-295.
    38.王绍坤.烟草烘烤后野火病、赤星病病斑面积的变化研究.中国烟草,1992,(1):23-25.
    39.王绍坤,赵瑜,姜建文.磷钾肥对烟草野火病的影响.烟草科技,1991,(1):37-39.
    40.王绍坤,赵瑜,姜建文.氮肥对烟草野火病的影响研究初报.烟草科技,1994,(3):44.
    41.王生荣.不同黄瓜品种感染黑腥病菌后一些酶含量的变化.山东农业大学学报,1999,30增刊:179-182.
    42.王雅平,刘伊强,施磊等.小麦对赤霉病抗性不同品种的SOD活性.植物生理学报,1993,19:353-358.
    43.汪耀富,林学梧,朱长远等.TMV对田间烟草生理生化的影响.河南农业大学学报,1992,26增刊:126-130.
    44.王裕中,Miller JD,Neish GA.中国南京三个禾谷镰刀菌菌株所产生的毒素.植物病理学报,1989,19(1):40.
    45.吴畏,杨家书,常乃滔等.小麦长蠕孢菌毒素.真菌学报,1989,8(1):70-78.
    46.吴元华,文才艺,李浩戈等.烟草感染马铃薯Y病毒脉坏死株系后六种酶活性变化的研究.植物病理学报,1999,5(2):30-33.
    47.吴岳轩,曾富华,王荣臣.杂交稻对白叶桔病的诱导抗性与细胞内防御酶系统关系的初步研究.植物病理学报,1996,26(2):127-131.
    48.夏正俊,顾本康,吴蔼民等.棉花品种抗黄萎病性与体内生化成分相关分析.植物保护学报,1994,21(4):305-310.
    49.徐建华,利容千,王建波.黄瓜不同抗病品种感染镰刀菌枯萎病菌后几种酶活性的变化.植物病理学报,1995,25(3):239-242.
    50.徐朗莱,叶茂炳,徐雍皋等.过氧化物酶及同工酶与小麦抗赤霉病性的关系.植物病理学报,1991,21(4):285-289.
    51.袁美丽,高洁,张佳环等.烟草上四种细菌病害的鉴别.中国烟草,1992,(3):37-39.
    52.袁美丽,高洁,张佳环等.烟草野火病药剂防治研究.吉林农业大学学报,1994,16(4):18-23.
    53.杨家书.植物苯丙氨酸类代谢与小麦对白粉病抗性的关系.植物病理学报,1986,16(3):169-173.
    54.叶茂炳,徐朗莱,徐雍皋等.苯丙氨酸解氨酶和绿原酸与小麦抗赤霉病性的关系.南京农业大学学报,1990,13(3):103-107.
    55.叶钟音,刘经芬.水稻对白叶枯病菌(Xanthomonas campestris pv.oryzae)的抗性与过氧化物酶和过氧化物酶同工酶活性的关系.南京农学院学报,1984,(2):39-45.
    56.余叔之.植物生理与分子生物学.北京:科学出版社.1992,417-423.
    57.张世光.烟草野火病病原鉴定及品种抗病性的研究.云南农业大学学报.1990.5(3),185-187.
    58.张世光,陈惠明.11个烟草品种对烟草野火病菌的抗病性鉴定.烟草科技,1989,(1):43.
    59.章元寿主编.植物病理生理学.江苏:江苏科学技术出版社.1996.
    60.赵卫东,刘进元.烟草野火病菌的分子遗传.生物工程进展,1997,17(2):44-47.
    61.邹琦主编.植物生理生化实验指导.北京:中国农业出版社.1995.
    62.朱广廉,钟文海,张爱琴.植物生理学实验.北京:北京大学出版社,1991.
    63.Adam A,Farkas T,Somiyal G et al.Consequence of O_2· generation during a bacteria induced hypersensitive reaction in tobacco:Deterioration of membrane lipids.Physiology Molecular Plant Pathology,1989,34:13.
    64.Andre E,Hou K W.The presence of a lipoid oxidase in soybean.Glycine soya,Lieb C R Acad Sci,1932,194:645-647.
    65.Anzai H,Yoneyama K,Yamaguchi I.Transgenic tobacco resistant to a bacterial disease by the detoxification of a pathogenic toxin.Mol Gen Genet,1989,219:492-494.
    66.Baker CJ,O'Neill NR,Keppler LD et al.Early responses during plant-bacteria interactions in tobacco cell suspensions.Phytopathology,1991,81:1504.
    67.Baker CJ,Orlandi EW,Mock NM.Harpin,an elicitor of the hypersensitive response in tobacco caused by Erwinia amylovora,elicit active oxygen production in suspension cells.Plant Physiology,1993,102:1341.
    68.Bradliy DJ,Kjellbom P.,Lamb CJ.Elicitor and wound-induced oxidative cross-linking of a proline-rich plant cell protein:A novel rapid defense response.Cell,1992,70:21.
    69.Buonaurio R,Torre GD,Montalbini P.Soluble superoxide dismutase(SOD) in susceptible and resistant host-parasite complex of Paseolus nulgatis and Uromyces phaseoli.Physiology Molecular Plant Pathology,1987,31:173.
    70.Callow JA,et al.Biochemical Plant Pathology New York,Wiley,1983.
    71.Chai HB,Doke N.Activation of the potential of potato leaf tissue to react hypersensitive to Phytophora infestans cytospora germination fluid and the enhancement of this potential by calcium ions.Physiology Molecular Plant Pathology,1987,30:27.
    72.Chigrin,W.Oxidative,lipolytic and protective enzymes in the leaves of rust resistant and susceptible plants of wheat.Fiziologiya Rastenii,1988,35:1198-1208.
    73.Croft KPC,Voisey CR,Slusarenko AJ.Mechanisms of hypersensitive cell collapse:Correlation of increased lipoxygenase activity with membrane damage in leaves of Phaseolus vulogaris inoculated with an avirulent race of Pseudomonas syringae pv.Syringae.Physiol.Mol.plant Pathol.,1990,36:49.
    74.Deall MW and JS Cole.A comparative study of the pathogencity and epidemiology of trains of Pseudomonas syringae pv.tabaci that cause wildfire and angular leaf spot disease of tobacco in Zimbabwe.Plant Pathol,1986,35(1):74—81.
    
    75. Degouses N,Trantuphylides C,Montillet JL.Involvement of oxidative processes in the signaling mechanisms leading to the activation of glyceollin synthesis in soybean (Glycine max).PIant physiology. 1994,104:945.
    
    76. Doke N.Involvement of superoxide anion generation in the hypersensitive response of potato tuber tissue to infection with an incompatible race of Phytophthora infestans and to the hyphal wall components.Physiplogy Plant Pathology,1983,23:345.
    
    77. Doke N.NADPH~dependent O_2~(·~) generation in membrance fraction isolated from wounded potato tubers inoculated with Phytophthora infectans.PhysioIogy Plant Pathology,1985,27:311.
    
    78. Durbin RD.Bacterial phytotoxins:Mechanisms of action.Experientia,199l,47:776—783
    
    79. Ebote AU,Mayee CD.Biochemical changes in rust (Puccinia arachidis) resistant and susceptible varieties of groundnut after inoculation.Indian Phytopath.,1983,36(1):194.
    
    80. Faby PC,GJ Persley.Plant Bacterial Disease ~ A Diagnostic Guide.SydneyrAcademic Press.1983.
    
    81. Gamm EL,Towers GHN.Review article phenylalanine ammonia lyase.Phytochemistry, 1973,12:961—973.
    
    82. Glazener JA,Orlandi EW,Harmon GL et al.An improved method for monitoring active oxygen in bacteria — treated suspension cells using luminol ~ dependent chemiluminescene.Physiology Molecular Plant Pathology, 1993,42:221.
    
    83. Goodman RN, et al.The Biochemistry and Physiology of Plant Disease.University of Missouri Press, 1986.
    
    84. Grgen NE,Hadwiger LA,Graham SO .Phenylalanine ammonia lyase,chloerogenic acid and lignin in potato tubertissue inoculated with Phytophthora infectans.Plant Pathology, 1973,3(4):495—507.
    
    85. Grisebach H.The Biochemistry of Plant.Academic,New York:Vol 451.
    
    86. Howell CR,Stipanovio RD.Phytoxicity to Crop Plants and Herbicidal Effects on Weeds of Viridiol Produced by Gliocladium virens.1984,74(11):1346—1349.
    
    87. Kalsadia M. Snidies on the M ~ 83 strains for its antagonistic effect on Pseudomonas syringae pv.tabaci (Wolf & Foster) Young, Dge & Wilkie.Pochvozn Agrokhim Rastit Zasht,1987,22(6):59~62.
    
    88. Keppler LD,Baker CJ.O_2~(·~) initiated lipid peroxidation in a bacteria—induced hypersensitive reaction in tobacco cell suspensions.Phytopathology,1989,79:555.
    
    89. Keppler LD,Baker CJ.Atkinson MM.Active oxygen production during a bacteria—induced hypersensitive reaction in tobacco suspension cells.Phytotathology, 1989,79:974.
    
    90. Keppler LD,Novacky A.The initation of membrane lipid peroxidation during bacteria ~ induced hypersensitive reaction.Physiology Molecular Plant Pathology,1987,30:233.
    
    91. Kim KK,Fravel DR,Papavezas GC.Identification of a metabolite produced by Talaromyces flavusas glucose oxidase and its role in the biocontrol of Verticillium dahliae.Phytopathology, 1988,78:488.
    
    92. Koch E,Meter BM,Eiben H et al.Alipoxygenase from leaves of tomato (Lycopersicon esculentum Mill.) is induced in response to plant pathogenic pseudomonas.Plant Physiol.,1992,99:571.
    
    93. Koukol J,Conn EE.The metabolism of aromatic:compounds in higher plants IV . Purification and properties of the phenylalanine deaminase of Herdeum Vulagare. J.Biol. Chem., 1961,23:2692~2698.
    
    94. Lindgren PB.Molecular analysis of plant defense responses to plant pathogens.J. Nematol.,1992,24(3):330~337.
    
    95. Lovrekovich L,H Lovrekovich,MA Stahmann.Importance of peroxidase in the wildfire disease.Phytopathology,1968,58(2):193~198
    
    96. Lucas GB.Diseases of Tobacco(3~(rd) ed).Raleigh North Carolina,U.S.A.,1975,397~409.
    
    97. Mayer AM et al.Phytochemitery,1979,18:193~215.
    
    98. Mcintyre L et al.Importance of peroxidase in the wildfire disease.Phytopathology, 1968,158(2):193~198.
    
    99. Mehdy MC.Active oxygen species in plant disease against pathogens.Plant Physiology, 1994,105:467.
    
    100. Mitchell RE.The relevance of non~specific toxins in the expression of virulence by pathogens.Ann Rev Phytopathol,1984,22:215~245.
    
    101. Moore LW.Recent advances in the biological control of bacterial plant diseases.Biol Control Crop Prod.,1980,375~390.
    
    102. Nami T,Kato T,Yamaguchi Y et al.Cytotoxicity and anti~blast activity of hydroperoxide of linolenic acid produced by in vitro enzyme reaction using blasts-infected rice leaves.Annual Phytopathology Society Japan,1991,57:339.
    
    103. Nelson D.,et al.Anal. Biochem., 1972,49:474.
    
    104. Nemeth J.Changes in respiration rate of tobacco leaves infected with bacteria in relation to the hypersensitive reaction.Acta. phytopathol., 1967,2(4): 303~308.
    
    105. Overeen JC.Threlfall DR.Biochemical aspect of plant parasite relationships. Academic press, 1976,134.
    
    106. Peng M. Kuc J.Peroxidase~ generated hydrogen peroxide as a source of antiftmgal activity in vitro and on tobacco leaf disks.Phytophology,1992,82:696.
    
    107. Rogers KR,Albert F.Anderson AJ.Liod peroxidation is a consequence of elicitor activity.Plant Physiology,1988,86:547..
    
    108. Roy MA,Sasser M.Evidence for involvement of active oxygen in tobacco resistance to a bacterial pathogen.Phytopathology,1983,73:968.
    
    109. Ruzicska P,Gombos Z,Farkas G.Modification of the fatty acid composition of phospholipids during the hypersensitive reaction in tobacco.Virology,1983,128:60.
    
    110. Strange RN.Plant Disease Control,Chapman & Hall, 1993.
    
    111. Schaod,N.W., Laboratory guide for identification of plant pathogenic bacteria St.paul, minn. American pnychopathological. Society. 1980
    
    112. Svalheim O,Robertsen B.Elicitation of H_2O_2 production in cucumber hypocotyls segments by oligo~1,4~ α~D~galacturonides and an oligo~glucan preparation from cell wall of Phytophthora megasperma f. sp.Glycinea.Physiology Plant,1993,88:675.
    
    113. Thomas MD, Langston~Unkefer PJ,Uchytil TF et al.Inhibition of glutamine synthase from pea by tabtoxine~β~lactam.Plant Physiol,1983,71:912~915.
    
    114. Van Huystee, R.B.Ann.Rev.Plant physiology,1987,38:205~219.
    
    115. Veech, JA.Localization of peroxidase in infected tobacco susceptible and resistant to black shank.Phytopathology,59:566~571.
    
    116. Viakhov S.Antibiotic substances of actinom~ycetes against phytopathogenic bacteria. God Soffi Univ Biol Fak Kn 2 Bot Mikrobiol Fiziol Bioklin Rost,1971,72(66):89~102
    
    117. Wannamaker,M.J.,Rufty,R.C.Development of a method to evaluate tobacco genotypes for resistance to angular leaf spot in the greenhouse.Plant Disease, 73:964 ~ 968.
    
    118. Wojtaszek P.Oxidative burst:an early plant response to pathogen infection.Bichem J,1997,322:681~692.

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