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Beta Plant Introductions from the USDA-ARS NPGS evaluated for resistance to Cercospora beticola, 2014

机译:USDA-ARS NPGS的Beta植物引种评估了其对巴西锥尾孢的抗性,2014年

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Thirty Plant Introductions (PIs) from the USDA-ARS National Plant Germplasm System (NPGS) Beta Collection [includes garden beet, sugarbeet, leaf beet, fodder beet (Beta vulgaris L.), and wild beet (Beta spp.)] were evaluated for resistance to Cercospora beticola in an artificially produced epiphytotic environment (based generally on Ruppel, E.G. and J.O. Gaskill. 1971. J. Am. Soc. Sugar Beet Technol. 16:384). A randomized complete-block design, with three replications was used to evaluate germplasm at the Michigan State University Saginaw Valley Research and Extension Center (SVREC) near Frankenmuth, MI. The field had been planted in wheat with clover underseeded in 2013. Internal controls included a susceptible check, 12N0050 (kindly provided by L.Campbell), and a resistant check, EL50/2 (PI 664912). Single-row plots 4.5 m long, with 51 cm between rows were planted on 5 May. Moncut 70DF (flutolonil) was applied at 0.0091 kg/100 m row in a 14 cm band in-furrow at planting to control Rhizoctonia damping-off and Quadris 2.08SC (azoxystrobin) was applied at 0.0067 L/100 m row on 5 Jun-to manage Rhizoctonia crown and root rot with limited potential to impact leaf spot development. The nursery was spray-inoculated on 10 Jul with a liquid spore suspension (approximately 1 x 103 spores/ml as determined with a hemacytometer) of C. beticola. Inoculum was produced from a mixture of leaves collected from the 2013 inoculated leaf spot nursery at SVREC and naturally infected beets grown on the Michigan StateUniversity campus farms in East Lansing, MI. Visual evaluations of the plot with a disease index (DI) on a scale from 0-10 where 0=no symptoms, 1=a few scattered spots, 2=spots coalescing or in large numbers on lower leaves only, 3= some dieback on lower leaves, but leaves not entirely dead, 4-8 are increasing amounts of dead and diseased tissue, 9= mostly dead with few remaining living leaves with large dead patches, and 10=all leaves dead. Evaluations were made on 14, 21, and 28 Aug, and 3 Sep, withthe peak of the epidemic occurring around 3 Sep. An evaluation was attempted subsequently, but several PIs were losing leaves following production of seed stalks and others were showing new leaf growth following defoliation from Cercospora leaf spot, sothese ratings were not used. Weeds were controlled three times with mixtures of phenmedipham, desmedipham, triflusulfuron methyl, and clopyralid (1, 16, and 28 Jun) and once with S-metolachlor (28 Jun). Hand weeding was done as needed to control larger weeds. The beet crop was thinned by hand with the generous help of Michigan Sugar Cooperative. Bolting beets were removed throughout the season.
机译:对来自USDA-ARS国家植物种质系统(NPGS)Beta集合的三十种植物引种(PI)进行了评估[包括花园甜菜,甜菜,叶甜菜,饲料甜菜(Beta vulgaris L.)和野生甜菜(Beta spp。)]。在人工产生的附生环境中对番茄斜纹夜蛾的抗性(通常基于Ruppel,EG和JO Gaskill。1971. J. Am。Soc。Sugar Beet Technol。16:384)。在密歇根州弗兰肯默斯附近的密歇根州立大学萨吉诺谷研究与推广中心(SVREC),使用具有三个重复的随机完整区组设计来评估种质。该田地已于2013年播种了小麦,但未播种三叶草。内部控制措施包括易感检查12N0050(由L.Campbell提供)和抗性检查EL50 / 2(PI 664912)。 5月5日种植了4.5 m长,两行之间51 cm长的单行样地。在种植时向沟内14 cm处以0.0091 kg / 100 m的行数施用Moncut 70DF(氟托隆尼),以控制根瘤菌的阻尼作用,并于6月5日以0.0067 L / 100 m的行数施用Quadris 2.08SC(嘧菌酯)。应对根瘤菌冠和根腐病,影响叶斑发育的潜力有限。苗圃在7月10日用液体孢子悬浮液(按血细胞计数器测定,约为1 x 103孢子/ ml)进行喷雾接种。接种物是由SVREC的2013年接种点斑苗圃收集的叶子与密歇根州东兰辛市密歇根州立大学校园农场种植的自然感染的甜菜混合而成的。用0-10的疾病指数(DI)对图进行视觉评估,其中0 =无症状,1 =少量散斑,2 =仅在较低的叶子上聚结或大量斑点,3 =枯萎较低的叶片,但叶片不完全死,4-8具越来越多的死亡和患病组织,9 =多数死亡,剩下的活叶片很少,有大的死斑,10 =全部叶片死亡。在8月14日,21日,28日和9月3日进行了评估,该流行病的高峰发生在9月3日左右。随后尝试进行评估,但是一些PI在种子茎产生后失去了叶片,而其他PI则显示出新的叶片生长从Cercospora叶斑上脱落后,未使用这些等级。用苯乙哌啶,去甲草胺,甲基三氟磺隆和氯吡格雷的混合物(6月1日,16日和28日)防治杂草3次,并用S-异丙甲草胺(6月28日)防治杂草。根据需要进行了手工除草,以控制较大的杂草。在密歇根糖业合作社的慷慨帮助下,甜菜作物被手工打薄。在整个季节中,抽出的甜菜被去除。

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