초록

○ 수출용 자생 Ardisia의 고품질 소형분화생산 기술 개발
○ 분화류 상품디자인 및 포장기술 개발
○ 자생나리 개량형 아시아틱나리 품종 육성
○ 개화기, 화색 및 화형이 다양한 용담 신품종 육성
○ 바위떡풀 신품종의 농가보급
○ 자생식물의 유전자원 평가 및 활용 연구
○ 화단 및 조경용 자생 화훼류의 증식 및 종묘생산에 관한 연구
○ 유망자생식물의 번식 및 재배 메뉴얼 제작

Abstract ▼

Chloranthus glaber (Thunb. Makino) is belongs to Chloranthaceae and it is an evergreen shrub with stems like bamboo. Generally, it is distributed in China, Taiwan, India, the Philippines and Japan. It is grown in the foothills of less than 700m and under a tree in the valley in Jeju, Also, it is kno

Chloranthus glaber (Thunb. Makino) is belongs to Chloranthaceae and it is an evergreen shrub with stems like bamboo. Generally, it is distributed in China, Taiwan, India, the Philippines and Japan. It is grown in the foothills of less than 700m and under a tree in the valley in Jeju, Also, it is known as the only indigenous plants half-shade. Currently It has been designated as wild plants by the Ministry of Environment. and it was restored in the valley of the Seogwipo Donnaeko. t is mainly are grown as cut flowers in the some southern part of Jeju because it is hardy in our country, in urban areas are known to be difficult to adapt plant. Chloranthus glaber has the scent of the flowering period and red berries, leaves and stems can be enjoyed together in winter. It has the advantage of using as small pot-plants of indoors because plants do not require a lot of light and it has almost no disease and pests. This research carried out to investigate technique for propagation and dwarf growing of plant growth regulator, temperature, and media. As a results, suitable cutting method was cutting in sand after dipping the IBA 1,000 ppm solution for 60 seconds. Bonzi and decomposition of granite were the most effective plant growth regulator and media in Chloranthus glaber dwarfing. Depending on the temperature treatment, dwarfing of 1-year and 3-year Chloranthus glaber were effective in 10℃ and 5℃ for 120 days treatment, respectively. Shoots of Chloranthus glaber were formed when TDZ 10 ppm was treatment. Seeds in green-house were germinated more than about 95% after 8 weeks but seeds in vitro were germinated 80% after 10-12 weeks. Tissue culture was effective at the apical meristem culture and Number of shoots and lateral branches increased although it takes a long time rather than the seed germination. Thus, it will be beneficial when subcultured.

목차 Contents

• 표지 ... 1
• 제출문 ... 2
• 요약문 ... 3
• SUMMARY ... 5
• 제 1 장 서 론 ... 11
• 제1절 연구개발의 목적, 필요성 및 범위 ... 11
• 제 2 장 국내외 기술개발 현황 ... 16
• 제1절 국·내외 관련분야에 대한 기술개발현황 ... 16
• 제 3 장 연구개발 수행 내용 및 결과 ... 21
• 제1절 재료 및 방법 ... 21
• 제2절 연구내용 및 결과 ... 35
• 제 4 장 연구개발목표 달성도 및 대외기여도 ... 143
• 제1절 목표대비 달성도 ... 143
• 제2절 정량적 성과 ... 143
• 제 5 장 연구개발결과의 활용계획 ... 148
• 제 6 장 기타 중요 변동사항 ... 149
• 제 7 장 참고문헌 ... 150