우리나라에서의 벼 줄무늬잎마름병의 발생, 피해, 기생범위, 전염 및 방제에 관하여 1965년부터, 1974년까지 실시한 연구결과를 다음과 같이 보고한다. 1. 발생 못자리에서 줄무늬잎마름병의 피해는 였고 포장에서는 입도중의 발병주율보다 재생도에서의 발생율이 높았으며 보통기재배보다도 조기재배에서 발병이 많았다. 또 포장에서 발병주의 분포는 대체로 휴반가까이에 많은 경향이었다. 벼 엽기별 피해에서 라병성인 일본계 벼의 경우 못자리 때인 3엽기에서 7엽기까지는 감염되면 고사하였으며 9엽기에서는 , 11엽기는 , 13엽기 이후에는 고사주를 볼 수 없었다. 참복기간은 3-7엽기에서는 7-15일이었고 9-15엽기에서는 15-30일이었다. 저항성인 통일벼의 경우 1.5-5엽기 접종구는 비교적 발병이 많았으나 9엽기 이후부터는 현저히 떨어져 15엽기 이후는 발병을 거의 볼 수 없었다. 그리고 감염된 것은 초장이 짧고 등숙율과 임실비율이 떨어지는 경향이었다. 2. 기주범위 기주범위를 구명하기 위하여 작물과 목초 및 잡초 36종을 공시하여 아래와 같이 21종의 기주를 밝혀 내었다. 작물: 벼, 보리, 밀 , 귀리, 라이맥, 조, 옥수수, 기장, 참피 목초: 티모시, 빗살대, 이타리안라이그라스, 패래니 알라이그라스, 죤슨그라스, 슈단그라스 잡초 : 들피, 겨피, 방울피, 잠자리피, 개미피, 바랭이, 민바랭이, 좀바랭이, 방동사니대가리, 강아지풀, 비노리, 참새, 포아풀, 독새풀, 우산대바랭이, 개보리, 겨풀, 쇠풀, 조개풀, 넓은 잎 개수염은 새로운 기주로 밝혀졌다. 3. 충매전염 우리나라의 애멸구화기는 5회였으며 수원에서의 제2회성충 최성기는 6월 20일 경이고 제3회성충 최성기는 7월 30일 경이었다. 진주는 수원보다 제2회성충 최성기가 5-7일 빨랐고 진주에서는 제3회성충 최성기의 발생량이 많은 것이 달랐다. 애멸구 세대별 보독충율은 월동약충이 였고 제1세대유충은 , 제2회성충은 , 제2세대유충은 , 나머지 화기에서는 약 였는데 보독충율은 남부지방보다 높은 경향이었다. 1966년부터 1970년생 사이의 애멸구 보독충율은 해에 따라 다소 차가 있었으며 화기별로는 제2회성충과 제3회성충의 보독충율이 높았다. 분리한 애멸구보독충을 재분리하여 이를 교배하였더니 차대에서는 보독충율이 인 애멸구를 얻을 수 있었으며 애멸구충령별로는 3, 4, 5령충의 감염능력이 높았고 애멸구 무독충의 바이러스 재획득율은 평균였고 여기에서 얻어진 친화성계통이라 할지라고 3회접종시험결과 계속하여 3회까지 벼에 바이러스를 매개하지 않았다. 또 애멸구보독충의 감염최적온도는 였으며, 이하에는 감염이 일어나지 않을때도 있었다. 그리고 애멸구기생봉의 기생율은 6월부터 8월말까지 였으며 7월 10일경이 로서 가장 높았다.

The study has been carried out to investigate the occurrence, damage, host range, transmission and control of rice stripe virus in Korea since 1965. 1 Disease occur「once and damage : The virus infection during the seedling stage ranged from 1.3 to . More symptom expression was found in regrowth of clipped rice than infected intact plants, and the greater infection took place in early seasonal culture than in ordinary seasonal culture. A higher incidence of the disease was found on the rows close to the bank, and gradually decreased toward the centre of the rice paddy. Disease occurrence and plant maturity was highly correlated in that the most japonica rice types were diseased when they were inoculated within 3 to 7 leaf stage, and, and no diseaseb were found if they were inoculated at 9, 11 and 13 leaf stages, respectively. Symptom expression required 7-15 days when the plants were inoculated during 3-7 leaf stages, while it was 15-30days in the plants inoculated during 9-15 leaf stages. On Tongil variety the per cent disease was relatively higher when the plants were infected within 1.5-5 leaf stages than those at 9 leaf stage, and no disease was found on the plants infected after 15 leaf stage. The disease resulted in lowered growth rates, maturity and sterility of Tongil variety although the variety is known as tolerant to the virus. 2. Host range: Thirty five species of crops, pasture grasses and weeds were tested for their susceptibility to the virus. Twenty one out of 35 species tested were found to be susceptible. and 3 of them, Cyperus amuricus Maximowics var. laxus, Purcereus sanguinolentus Nees and Eriocaulon robustius Makino, were found as new hosts of the virus. 3. Transmission: The vector of the virus, Laodelphax striatellus, produces 5 generations a year. The peak of second generation adults occurred at June 20th and those of third was at about July 30th in Suweon area. In Jinju area the peak of second generation adult proceeded the peak at Suweon by 5-7 days. The peaak of third generation adult was higher than the second at Jinju, but at Suweon the reverse was true. The occurrence of viruliferous Laodelphax striatellus was 10-15, 9, 17, 8 and about from overwintered nymph, 1st generation nymph, 2nd generation adult, End generation nymph and the remaining generations, respectively. More viruliferous L. striatellus were found in the southern area than in the central area of Korea. The occurrence of viruliferous L. striatellus depended on the circumstances of the year. The per cent viruliferous vectors gin 2nd and 3rd generation adult, however, was consistantly higher than that of other generations. Matings of viruliferous L. striatellus resulted in viruliferous progenies, and the 3rd, 4th and 5th instars of the vector had higher infectiviey than the rest of the vector stages. The virus acquisition rate of non-viruliferous L. striatellus was , These viruliferous L. striatellus, however, could not transmit the virus for more than 3 serial times. The optimum temperature for the transmission of the viru3 was , while rare transmission occurred when the temperature was below . The per cent of L. striatellus parasitization by Haplogonatopus atratus were during the period from June to the end of August, and the maximum parasitization was at around July 10. 4. Control: 1) Cultural practices, The deeper the depth of transplanting more the disease occurrence was found. The higher infection rate, , was observed during the late stages of seedling beds, and the rate became lower, , in the early period of paddy field in southern area. Early transplanting resulted in more infection than early seasonal culture, and the ordinary seasonal culture showed the lowest infection. The disease also was favored by earlier transplanting even under tile ordinary seasonal culture. The higher the nitrogen fertilizer level the more the disease occurrence was found in the paddy field. 2) Resistant varieties, Tongil varieties shelved the resistant reaction to the virus in greenhouse tests. In the tests for resistance on 955 varieties most japonica types shelved susceptible reactions, while the resistant varieties were found mostly from introduced varietal groups. 3) Chemical control, Earlier applications of chemicals, Disyston and Diazinon, showed better results when the test was made 4 days after inoculation in the greenhouse even though none of the insecticides shelved the complete control of the disease. Three serial applications of chemicals on June 14, June 20 and June 28 showed bettor results than one or two applications at any other dates under field conditions.

• 鄭鳳朝