• Title/Summary/Keyword: chestnut insect

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Confirmation of Chestnut Powdery Mildew, Erysiphe castaneigena, in Korea with Morphological Characteristics and Molecular Analyses (형태적 특징 및 분자적 분석에 의한 밤나무 흰가루병균 Erysiphe castaneigena의 확인)

  • Cho, Sung-Eun;Lee, Sang-Hyun;Lee, Sun Keun;Shin, Hyeon-Dong
    • The Korean Journal of Mycology
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    • v.45 no.2
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    • pp.145-152
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    • 2017
  • The powdery mildew on Castanea crenata in South Korea was first recorded as Microsphaera alni in 1958. On the basis of its morphological characteristics and host range, the mildew was determined as Microsphaera sinensis in 1988. According to the rules of The International Code of Botanical Nomenclature, M. sinensis was renamed Erysiphe castaneigena in 2006. Nevertheless, taxonomic re-consideration of the morphological and molecular characteristics for the Castanea powdery mildew in Korea has not been performed. In the present study, we studied 34 powdery mildew samples collected from C. crenata in the Korea University Herbarium. On the basis of microscopic examinations of the holomorph and phylogenetic analysis of the internal transcribed spacer regions, we confirmed the powdery mildew fungus as E. castaneigena. In addition, sequence comparison between E. castaneigena and E. alphitoides ex Castanea sp. suggested a close phylogenetic affinity.

Pathogenicity of Korean Entomopathogenic Nematodes (Steinermematidae and Heterorhabditidae) against Local Agricultural and Forest Insect Pests (한국산 곤충병원성 선충 (Steinernematidae와 Heterorhabditidae)의 지역농림해충에 대한 병원성)

  • 추호렬;이상명;정부근;박영도;김형환
    • Korean journal of applied entomology
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    • v.34 no.4
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    • pp.314-320
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    • 1995
  • Pathogenicity of Korean entomopathogenic nematodes against local insect pests was different depending on strains or target-insect pests. Mortalities of diamondback moth, Plutella xylostella larvae were 51.8%, 77.8%, 96.3% or 100% in Hanrim Steinernema sp. and 50.0%, 74.1%, 96.3% or 98.1% in Hamyang Heterorhabditis sp. on filter paper when larvae were exposed to 3, 6, 12, or 24 nematodes per larva. Mortalities of them on kale leaves at the same concentration were 44.4%, 63.0%, 76.1%, or 94.5% in Hanrim Steinernema sp. and 79.7%, 81.6%, 94.4%, or 100% in Hamyang Heterorhabditis sp., respectively. In field test, control value of Hanrim Steinernema sp. was 72.0% and that of Hamyang Heterorhabditis sp. was 84.1% in 14 days when 300,000 nematodes were sprayed to each plot ($13.27\m^2$). Although mortalities of rice stem borer, Chilo suppressalis larvae showed no difference at high concentration, Hamyang Heterorhabditis sp. (47.3~100%) was more effective than Hanrim Steinernema sp. (34.3~83.3%) at low concentration, 50~200 nematodes/ml. When chestnut curculio, Curculio sikkimensis larvae were treated with Sancheong Steinernema sp. and Hamyang Heterorhabditis sp., respectively. When pellucid zygaenid, Pryeria sinica larvae were exposed to nematodes, Pocheon Steinernema sp. was effective ranging from 96.7% to 100% but mortalities of them were 63.3~76.7% in Dongrae Steinernema sp..

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Damage of Perennial Ryegrass, Lolium perenne by Chestnut Brown Chafer, Adoretus tenuimaculatus (Coleoptera: Scarabaeidae) and Biological Control with Korean Isolate of Entomopathogenic Nematodes (주둥무늬차색풍뎅이(Adoretus tenuimacuiatus)에 의한 퍼레니얼라이그라스(Lolium perenne)피해와 한국산 곤충병원성 선충을 이용한 생물적 방제)

  • 이동운;추호렬;신옥진;윤재수;김영섭
    • Korean journal of applied entomology
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    • v.41 no.3
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    • pp.217-223
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    • 2002
  • The chestnut brown chafer, Adoretus tenuimaculatus Waterhouse, is serious insect pests in golf courses. Adults feed on the leaves of latifoliate trees but larvae feed on roots of turfgrases such as bentgrass, Agrostis spp. Damage of A. tenuimaculatus larvae was observed at the Jinju golf club which showed damage symptom on perennial ryegrass, Lolium perenne in tees and fairways in July, 2000. Damaged turf by A. tenuimaculatus larvae became yellowish and wilted. Symptom of laval damage of A. tenuimaculatus was similar to summer depression in warm season turfgrasses but not recovered by irrigation when Korean isolates of entomopathogenic nematodes were evaluated for the control of A. tenuimaculatus larvae in laboratory and field as a possible biological control agent. The nematodes used were Heterorhabditis bacteriophora Jeju strain, Hererorhabditis sp. Gyeongsan strain, Steinernema carpocapsae Pocheon strain, S.glaseri Dongrea strain, and S.longicaudum Nonsan strain. In the laboratory test H.bacreriophora Jeju strain and Heterorhabditis sp. Gyeongsan strain were highly effective for 3rd instars with 95% mortality. In the field test reduction rates of A.tenuimaculatus larvae were higher by ranging from 28 to 57% by H. bacteriophora Jeju strain, Heterorhabditis sp. Gyeongsan strain, and S.carpocapsae Pocheon strain compared to 7% by natural cause.

In vivo Pathogenicity Test of Oak Wilt Fungus (Raffaelea quercus-mongolicae) on Oriental Chestnut Oak (Quercus acutissima)

  • Yi, Su Hee;Lee, Jin Heung;Seo, Sang Tae;Lee, Jong Kyu
    • Journal of Forest and Environmental Science
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    • v.33 no.4
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    • pp.342-347
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    • 2017
  • Since the first report of the oak wilt disease at 2004 in Korea, the disease distributed over Korean peninsula and are still giving severe damages. The management of oak wilt disease in Korea has mainly focused on the control of insect vector, Platypus koryoensis. Neverthless the effective method for evaluating the pathogenicity of the pathogen, Raffaelea quercus-mongolicae (Rqm), and for screening chemical or biological agents with strong inhibitory activity against the pathogen, is absolutely necessary, an reliable method is not available so far. This study was conducted to develop the effective method for evaluating the pathogenicity of Rqm in oak trees. The culture suspensions of Rqm were artificially injected to the saplings of Quercus acutissima by using ChemJet tree injector. Three months after treatments, the treated saplings were cut and dipped into 1% fuchsin acid solution. There were significant differences in non-conductive area (%), discoloration area (%) and vertical discoloration length between the pathogen-injected and distilled water-injected control treatments. These results indicated that the pathogen is the causal agent for the dysfunction of water conductive tissue, which will finally result in wilt symptom. Re-isolation of the pathogen and PCR detection using specific primers for the pathogen also confirmed the presence of Rqm in the sapwood chips of the pathogen-injected saplings. These observations would be greatly applied to other related researches for evaluating the pathogenicity of tree wilt pathogens and biocontrol efficacy of the selected antagonistic microorganisms, in case that the wilt symptom is not easily shown by artificial inoculation of the causal agent.

Molecular Characteristics of Phytophthora katsurae Using PCR-SSCP Analysis (PCR-SSCP 분석에 의한 Phytophthora katsurae의 분자생물학적 특성)

  • Lee, Sun-Keun;Jang, Ha-Na;Lee, Dong-Hyeon;Lee, Sang-Hyun;Lee, Sang-Yong;Lee, Jong-Kyu
    • Research in Plant Disease
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    • v.17 no.2
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    • pp.169-176
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    • 2011
  • Phytophthora katsurae is the fungus responsible for chestnut ink disease. The objectives of this study were to determine if a single-strand conformation polymorphism (SSCP) analysis of rDNA-ITS region, elongation factor 1 alpha gene and ${\beta}$-tubulin gene could be used for rapid identification and genetic diversity of P. katsurae, and to assess the potential use of the SSCP technique as a diagnostic tool for P. katsurae. Each regions amplified by PCR using primers designed to overlap the genus Phytophthora were characterized for the Phytophthora species. PCR products were denatured and electrophoresed for SSCP analysis. P. katsurae isolates showed an unique pattern in SSCP analysis and were easily distinguished from other Phytophthora species used as the control. This indicates that SSCP analysis is an useful technique for distinguishing Phytophthora species from genetically close relatives, and show that the SSCP analysis of each region is an efficient detection tool for P. katsurae. But PCR-SSCP analysis of single-gene may have difficulty in distinguishing P. katsurae from other Phytophthora species. Therefore, PCR-SSCP analysis of multi-genes can be useful for rapid and effective identification of P. katsurae.