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Evaluation of multiple biological control organisms for control of grey mold of tomato, 2006

机译:评价多种生物防治生物防治番茄灰霉病的方法,2006年

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An experiment testing different biological control organisms for the control of Botrytis grey mold of tomato was conducted at the Plant Growth Center at the Montana State University, MT. Six-week-old tomato plants grown in oasis cubes were transplanted into Coconut EZ Gro Bags (Hydro-Gardens, CO) and irrigated with a single dripper (flow rate 7.9 l/hr). The experiment used a randomized complete block design with 12 replications. Sixty bags were placed in five rows 0.6 m apart. The space of the bags within the row was also 0.6 m. The plants were kept at 24 deg C day and 16 deg C night temperatures with a 16 hr photoperiod (GE Multi-Vapor MVR1000/C/U). Treatments to control grey mold included an untreated control (plants sprayed with de-ionized water alone), Bacillus mojavensis isolate 203-7 (10e8 colony forming units/ml de-ionized water), Bacillus mycoides isolate BmJ (10e8 colony forming units/ml de-ionized water), Serenade Max (Bacillus subtilis strain QST 713, at a concentration of 2.5%), and PlantShield HC (Trichoderma harzianum strain KRL - AG2, at a rate of 3.8 g/l de-ionized water). Stem wounds caused by pruning were inoculated with a Botrytis cinerea conidia solution (10e7 conidia/ml in de-ionized water supplemented with 62.5 mM KH2PO4 and 5.5 mM Glucose, sprayed to run off). Inoculation was followed by overhead mist-irrigation to increase the humidity and to establish Botrytis stem canker infection. The mist-irrigation was applied every night for 12 hr in 30 min intervals for 30 sec duration. The first foliar application of treatments was conducted at 22 Nov 05 and successive sprays were applied weekly through 21 Feb 06. Yield data were collected over several weeks by harvesting and weighing ripe tomatoes until 4 Mar 06. Disease data for the leaf infections were collected on 11 Feb 06 and 28 Feb 06 by following rating scale (0-5) to estimate the percentage of leaf area covered by leasons on 10 individual leaves per plant: 0 = no lesions, 1 = multiple single lesions (> 10%), 2 = 25%, 3 = 50%, 4 = 75%, 5 = whole leaf covered (100%). Botrytis stem canker ratings were conducted at a weekly interval starting on 3 Jan 06 until 31 Jan 06, and at 14 Feb 06 and 28 Feb 06 by estimating the disease progress using following rating scale: 0 = no stem canker, 1 = lesion present, 2 = water soaking of lesion, 3 = water soaking extends into stem tissue, 4 = stem infected, 5 = stem girdled by canker.
机译:在蒙大拿州立大学的植物生长中心进行了一项实验,测试了不同的生物防治生物来控制番茄的葡萄孢灰霉病。将在绿洲立方体中生长的六周龄番茄植株移植到Coconut EZ Gro Bags(Hydro-Gardens,CO)中,并用单个滴头灌溉(流速7.9升/小时)。实验使用了具有12个重复的随机完整块设计。将六十个袋子放在相距0.6 m的五行中。行中的袋子间距也为0.6 m。将植物在24摄氏度的白天和16摄氏度的夜间温度下保持16小时的光周期(GE Multi-Vapor MVR1000 / C / U)。防治灰霉病的处理方法包括未经处理的对照(仅用去离子水喷雾的植物),莫桑德芽孢杆菌分离株203-7(10e8集落形成单位/ ml去离子水),霉菌芽孢杆菌分离BmJ(10e8集落形成单位/ ml)。去离子水),Serenade Max(枯草芽孢杆菌菌株QST 713,浓度为2.5%)和PlantShield HC(哈茨木霉菌株KRL-AG2,去离子水含量为3.8 g / l)。将修剪引起的茎伤口接种灰葡萄孢菌分生孢子溶液(在补充有62.5 mM KH2PO4和5.5 mM葡萄糖的去离子水中以10e7分生孢子/ ml喷雾,以流失)。接种后进行高架雾灌溉,以增加湿度并建立葡萄孢茎枯萎病感染。每晚以30分钟的间隔进行30小时的间隔12小时的薄雾灌溉。第一次叶面处理是在05年11月22日进行的,每周连续喷施直至06年2月21日。通过收获和称重成熟的西红柿直到06年3月4日,收集了数周的产量数据。由06年2月11日和2006年2月28日,按照评分等级(0-5)来估计每棵植物10片叶子上的叶子覆盖的叶子面积百分比:0 =无病害,1 =多个单一病害(> 10%),2 = 25%,3 = 50%,4 = 75%,5 =全叶覆盖(100%)。从2006年1月3日至06年1月31日,以及从06年2月14日至2月28日,每周进行Botrytis枯萎病等级评估,方法是使用以下等级量表评估疾病进展:0 =无枯萎病,1 =存在病变, 2 =病灶浸水,3 =浸润进入茎组织,4 =受感染的茎,5 =溃疡病引起的茎周围散裂。

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