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澳大利亚芥菜上由十字花科白粉菌引起的白粉病的首次报道

First Report of Powdery Mildew Caused by Erysiphe cruciferarum on Brassica juncea in Australia.

作者信息

Kaur P, Li C X, Barbetti M J, You M P, Li H, Sivasithamparam K

机构信息

School of Plant Biology, Faculty of Natural and Agricultural Sciences, The University of Western Australia, Crawley, W.A. 6009, Australia.

Department of Agriculture and Food of Western Australia, Baron-Hay Court, South Perth, W.A. 6151, Australia.

出版信息

Plant Dis. 2008 Apr;92(4):650. doi: 10.1094/PDIS-92-4-0650C.

DOI:10.1094/PDIS-92-4-0650C
PMID:30769625
Abstract

In Australia, Brassica juncea (L.) Czern & Coss (Indian mustard) has the potential as a more drought-tolerant oilseed crop than the B. napus L., with the first canola-quality B. juncea varieties released in Australia in 2006 and first sown for commercial production in 2007. Increased production of B. juncea is expected to result in the appearance of diseases previously unreported in Australia. In the spring of 2007 at the University of Western Australia field plots at Crawley (31.99°S, 115.82°E), Western Australia, plants of B. juncea genotypes from Australia and China had extensive stem colonization by powdery mildew at the end of the flowering period, with whitish patches ranging in size from 3 mm to 3 cm long. These patches coalesced to form a dense, white, powdery layer as they expanded. Pathogenicity was demonstrated by gently pressing infected stems containing abundant sporulation onto leaves of potted B. juncea seedlings of variety JM-18, incubating the plants in a moist chamber for 48 h, and then maintaining the plants in a controlled-environment room at 18/13°C for day/night. Signs of powdery mildew appeared at 7 days after inoculation, and by 10 days, it was well developed. Uninoculated control plants did not have powdery mildew. When symptomatic plants were examined, abundant conidia were typical of Erysiphe cruciferarum Opiz ex Junell, with cylindrical conidia borne singly or in short chains as described previously (2). Mycelia were amphigenous, in patches, and often spreading to become effused. Conidiophores were straight, foot cells were cylindrical, and conidia were mostly produced singly and measured 21.2 to 35.4 (mean 26.7 μm) × 8.8 to 15.9 μm (mean 11.9 μm) from measurements of 100 conidia. The spore size that we measured approximated what was found for E. cruciferarum (2) (30 to 40 × 12 to 16 μm), since we found 35 and 50% of spores falling within this range in terms of length and width, respectively. Conidia were, however, generally smaller in size than that reported on broccoli raab in California (1) (35 to 50 × 12 to 21 μm). We confirmed a length-to-width ratio greater than 2 as was found previously (1,2). Infected leaves showed signs of early senescence. While powdery mildew caused by E. cruciferarum is an important disease of B. juncea in India where yield losses as much as 17% have been reported (4), its potential impact in Australia is yet to be determined. To our knowledge, this is the first record of E. cruciferarum on B. juncea in Australia. In Western Australia, E. cruciferarum has been recorded on B. napus (oilseed rape) since 1986 and on B. napus L. var. napobrassica (L.) Reichenb. (swede) since 1971 (3). In other regions of Australia, it has been recorded on B. rapa in Queensland since 1913 and on B. napus (oilseed rape) in South Australia since 1973. References: (1) S. T. Koike and G. S. Saenz. Plant Dis. 81:1093, 1997. (2) T. J. Purnell and A. Sivanesan. No 251 in: Descriptions of Pathogenic Fungi and Bacteria. CMI, Kew, Surrey, UK, 1970. (3) R. G. Shivas. J. R. Soc. West. Aust. 72:1, 1989. (4) A. K. Shukla et al. Manual on Management of Rapeseed-Mustard Diseases. National Research Centre on Rapeseed-Mustard, Bharatpur, India, 2003.

摘要

在澳大利亚,芥菜型油菜(Brassica juncea (L.) Czern & Coss)作为一种比甘蓝型油菜(B. napus L.)更耐旱的油料作物具有潜力,2006年澳大利亚发布了首个符合油菜籽品质标准的芥菜型油菜品种,并于2007年首次播种用于商业生产。预计芥菜型油菜产量的增加将导致澳大利亚此前未报告过的病害出现。2007年春季,在西澳大利亚大学位于克劳利(南纬31.99°,东经115.82°)的田间试验地,来自澳大利亚和中国的芥菜型油菜基因型植株在花期结束时茎部被白粉菌广泛侵染,出现大小从3毫米到3厘米不等的白色斑块。这些斑块随着扩展会融合形成一层浓密的白色粉状物。通过将含有大量孢子形成的感染茎轻轻按压在盆栽的JM - 18品种芥菜型油菜幼苗叶片上,在湿度箱中培养48小时,然后将植株置于18/13°C(日/夜)的可控环境室中,证明了其致病性。接种后7天出现白粉病症状,到10天时病情已充分发展。未接种的对照植株未出现白粉病。检查有症状的植株时,大量分生孢子是十字花科白粉菌(Erysiphe cruciferarum Opiz ex Junell)的典型特征,圆柱形分生孢子单个着生或呈短链状,如先前所述(2)。菌丝体两面生,呈斑块状,且常扩展融合。分生孢子梗直,基部细胞圆柱形,分生孢子大多单个产生,从100个分生孢子的测量数据来看,其大小为21.2至35.4(平均26.7μm)×8.8至15.9μm(平均11.9μm)。我们测量的孢子大小与十字花科白粉菌(2)(30至40×12至16μm)的测量结果相近,因为我们发现分别有35%和50%的孢子在长度和宽度方面落在这个范围内。然而,分生孢子的大小通常比加利福尼亚州报道的抱子芥上的分生孢子(1)(35至50×12至21μm)小。我们确认长宽比大于2,这与之前的发现(1,2)一致。受感染的叶片表现出早期衰老的迹象。虽然十字花科白粉菌引起的白粉病是印度芥菜型油菜的一种重要病害,据报道产量损失高达17%(4),但其在澳大利亚的潜在影响尚未确定。据我们所知,这是澳大利亚首次记录到十字花科白粉菌侵染芥菜型油菜。在西澳大利亚,自1986年起就在甘蓝型油菜(油菜籽)上记录到十字花科白粉菌,自1971年起就在芜菁甘蓝(B. napus L. var. napobrassica (L.) Reichenb.)上记录到该菌(3)。在澳大利亚的其他地区,自1913年起在昆士兰州的白菜型油菜上以及自1973年起在南澳大利亚的甘蓝型油菜(油菜籽)上记录到该菌。参考文献:(1)S. T. Koike和G. S. Saenz。植物病害81:1093,1997。(2)T. J. Purnell和A. Sivanesan。载于《病原真菌和细菌描述》第251号。英国皇家植物园邱园真菌研究所,萨里,英国,1970。(3)R. G. Shivas。西澳大利亚皇家学会会刊72:1,1989。(4)A. K. Shukla等人。油菜 - 芥菜病害管理手册。印度巴拉特普尔油菜 - 芥菜国家研究中心,2003。