{"title":"安卡什卡拉兹谷地吉思兰茎基腐病病原学及防治","authors":"R. Aguilar-Anccota, L. Mattos-Calderon","doi":"10.21704/pja.v4i1.1461","DOIUrl":null,"url":null,"abstract":"Gypsophila is an ornamental plant whose flowers are economically important, which is cultivated in the Callejon de Huaylas valley-Ancash. Recently, cultivated Gypsophila fields have shown diseased plants characterized by stem base rot, which has been followed by a reduction in vigor and the collapse and death of plants. Therefore, the objectives of this research were to describe the symptomatology of the disease, identify the causative agent of the disease, and prove how effective fungicides and biological control agents (BCA) are in controlling the disease using in vitro and field experiments. To isolate the pathogen, symptomatic plant tissue samples were washed, cut into small pieces, disinfected in 1% sodium hypochlorite solution for 1 min, rinsed twice with sterilized water, and air-dried on paper towels. The samples were seeded on Petri dishes containing potato dextrose agar media and incubated at 25 °C. A pathogenicity test was conducted in healthy Gypsophila seedlings, which were grown in a sterilized substrate, using mechanical inoculation on the stem base and agar disks colonized by the pathogen-mycelium. Then the pathogen was reisolated from symptomatic inoculated Gypsophila seedlings. The “poisoned medium” technique was used to conduct the in vitro fungicide test, while the “dual method” was used to conduct the bio controller’s test. The results of the pathogenicity test and in vitro and field experiments showed that Rhizoctonia solani is the causative agent of the stem base Gypsophila disease, and at both assayed doses, the fungicides Rovral, Benopoint, Parachupadera, Vitavax, and Homai completely inhibited the mycelial growth of R. solani. Moreover, the BCAs Trichoderma harzianum and T. viride showed higher in vitro growth rates than R. solani and completely colonized the pathogen-mycelium. Under field conditions, the incidence of the disease in field plots treated with T. harzianum was 12.5% lower than in the control treatment, which showed 51.28% incidence of the disease. In addition, Gypsophila plants harvested from plots treated with T. harzianum exhibited higher numbers of flower stalks per plant and a higher fresh weight compared to the control treatment.","PeriodicalId":283246,"journal":{"name":"Peruvian Journal of Agronomy","volume":"43 1","pages":"0"},"PeriodicalIF":0.0000,"publicationDate":"2020-04-29","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"1","resultStr":"{\"title\":\"Etiology and control of Gypsophila paniculata L. stem base rot in the Caraz Valley, Ancash\",\"authors\":\"R. Aguilar-Anccota, L. Mattos-Calderon\",\"doi\":\"10.21704/pja.v4i1.1461\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"Gypsophila is an ornamental plant whose flowers are economically important, which is cultivated in the Callejon de Huaylas valley-Ancash. Recently, cultivated Gypsophila fields have shown diseased plants characterized by stem base rot, which has been followed by a reduction in vigor and the collapse and death of plants. Therefore, the objectives of this research were to describe the symptomatology of the disease, identify the causative agent of the disease, and prove how effective fungicides and biological control agents (BCA) are in controlling the disease using in vitro and field experiments. To isolate the pathogen, symptomatic plant tissue samples were washed, cut into small pieces, disinfected in 1% sodium hypochlorite solution for 1 min, rinsed twice with sterilized water, and air-dried on paper towels. The samples were seeded on Petri dishes containing potato dextrose agar media and incubated at 25 °C. A pathogenicity test was conducted in healthy Gypsophila seedlings, which were grown in a sterilized substrate, using mechanical inoculation on the stem base and agar disks colonized by the pathogen-mycelium. Then the pathogen was reisolated from symptomatic inoculated Gypsophila seedlings. The “poisoned medium” technique was used to conduct the in vitro fungicide test, while the “dual method” was used to conduct the bio controller’s test. The results of the pathogenicity test and in vitro and field experiments showed that Rhizoctonia solani is the causative agent of the stem base Gypsophila disease, and at both assayed doses, the fungicides Rovral, Benopoint, Parachupadera, Vitavax, and Homai completely inhibited the mycelial growth of R. solani. Moreover, the BCAs Trichoderma harzianum and T. viride showed higher in vitro growth rates than R. solani and completely colonized the pathogen-mycelium. Under field conditions, the incidence of the disease in field plots treated with T. harzianum was 12.5% lower than in the control treatment, which showed 51.28% incidence of the disease. 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引用次数: 1
摘要
Gypsophila是一种观赏植物,其花具有重要的经济价值,种植在Callejon de Huaylas山谷- ancash。近年来,栽培的毒蝇田出现了以茎基部腐病为特征的病株,随后是活力下降和植株枯萎死亡。因此,本研究的目的是描述该病的症状,确定该病的致病因子,并通过体外和田间实验证明杀菌剂和生物防治剂(BCA)在控制该病方面的有效性。为分离病原菌,将有症状的植物组织样品洗净,切成小块,在1%次氯酸钠溶液中消毒1 min,用消毒水冲洗2次,然后用纸巾风干。将样品接种于含有马铃薯葡萄糖琼脂培养基的培养皿中,在25°C下孵育。采用机械接种的方法,将健康的Gypsophila幼苗培养在无菌的培养基上,在茎基部和菌丝体定殖的琼脂盘上进行致病性试验。然后从有症状接种的Gypsophila幼苗中重新分离病原体。采用“中毒培养基”技术进行体外杀菌剂试验,采用“双重法”进行生物控制剂试验。致病性试验及离体和田间试验结果表明,茄根丝核菌是茎基Gypsophila病的病原菌,在两个测定剂量下,杀菌剂Rovral、Benopoint、Parachupadera、Vitavax和Homai均能完全抑制茄根丝核菌的菌丝生长。此外,bcaas菌株哈兹木霉和绿霉的体外生长速度高于番茄木霉,并能完全定植病原菌菌丝。在田间条件下,哈氏弓形虫田间地块的发病率比对照(51.28%)降低12.5%。此外,与对照处理相比,在处理过的田块收获的Gypsophila植株表现出更高的单株花梗数和更高的鲜重。
Etiology and control of Gypsophila paniculata L. stem base rot in the Caraz Valley, Ancash
Gypsophila is an ornamental plant whose flowers are economically important, which is cultivated in the Callejon de Huaylas valley-Ancash. Recently, cultivated Gypsophila fields have shown diseased plants characterized by stem base rot, which has been followed by a reduction in vigor and the collapse and death of plants. Therefore, the objectives of this research were to describe the symptomatology of the disease, identify the causative agent of the disease, and prove how effective fungicides and biological control agents (BCA) are in controlling the disease using in vitro and field experiments. To isolate the pathogen, symptomatic plant tissue samples were washed, cut into small pieces, disinfected in 1% sodium hypochlorite solution for 1 min, rinsed twice with sterilized water, and air-dried on paper towels. The samples were seeded on Petri dishes containing potato dextrose agar media and incubated at 25 °C. A pathogenicity test was conducted in healthy Gypsophila seedlings, which were grown in a sterilized substrate, using mechanical inoculation on the stem base and agar disks colonized by the pathogen-mycelium. Then the pathogen was reisolated from symptomatic inoculated Gypsophila seedlings. The “poisoned medium” technique was used to conduct the in vitro fungicide test, while the “dual method” was used to conduct the bio controller’s test. The results of the pathogenicity test and in vitro and field experiments showed that Rhizoctonia solani is the causative agent of the stem base Gypsophila disease, and at both assayed doses, the fungicides Rovral, Benopoint, Parachupadera, Vitavax, and Homai completely inhibited the mycelial growth of R. solani. Moreover, the BCAs Trichoderma harzianum and T. viride showed higher in vitro growth rates than R. solani and completely colonized the pathogen-mycelium. Under field conditions, the incidence of the disease in field plots treated with T. harzianum was 12.5% lower than in the control treatment, which showed 51.28% incidence of the disease. In addition, Gypsophila plants harvested from plots treated with T. harzianum exhibited higher numbers of flower stalks per plant and a higher fresh weight compared to the control treatment.