Skip navigation

DSpace

機構典藏 DSpace 系統致力於保存各式數位資料(如:文字、圖片、PDF)並使其易於取用。

點此認識 DSpace
DSpace logo
English
中文
  • 瀏覽論文
    • 校院系所
    • 出版年
    • 作者
    • 標題
    • 關鍵字
    • 指導教授
  • 搜尋 TDR
  • 授權 Q&A
    • 我的頁面
    • 接受 E-mail 通知
    • 編輯個人資料
  1. NTU Theses and Dissertations Repository
  2. 生物資源暨農學院
  3. 森林環境暨資源學系
請用此 Handle URI 來引用此文件: http://tdr.lib.ntu.edu.tw/jspui/handle/123456789/33937
完整後設資料紀錄
DC 欄位值語言
dc.contributor.advisor張上鎮(Shang-Tzen Chang)
dc.contributor.authorSen-Sung Chengen
dc.contributor.author鄭森松zh_TW
dc.date.accessioned2021-06-13T05:49:29Z-
dc.date.available2007-07-10
dc.date.copyright2006-07-10
dc.date.issued2006
dc.date.submitted2006-07-07
dc.identifier.citation王守範、王振瀾、謝堂州、曲俊麒(1987)省產主要木材之抗白蟻性與藥劑防止白蟻效能之研究。林業試驗所研究報告季刊 2:117-128。
王升陽、張上鎮、蘇裕昌、郭悅雄(1997)臺灣杉抽出成分之研究。國立臺灣大學實驗林研究報告 11:67-81。
李春來、林秀彥(1986)樹葉精油成分之研究(一)—柳杉葉之精油成分。國立台灣大學農學院實驗林研究報告 169:1-7。
吳文希(1985)植物病理學。茂昌圖書有限公司。台北。1-50頁。
何琦琛、王振瀾、吳金村、林建宗、吳懷慧(1998)六種木材對美洲室塵蟎的抑制力探討。中華昆蟲 18:247-257。
林務局(1995)第三次臺灣森林資源及土地利用調查。林務局。258頁。
林童傑(1997)臺灣紅檜葉之成份研究。國立臺灣大學化學研究所博士論文。384頁。
林天書、張東柱(1999)兩種加拿大進口及三種國內木材之抗白蟻及耐腐性。臺灣林業科學 14:235-239。
吳金村、許建發(1988)木材加工與抽出成分。木工家具 43:53-61。
許龍麟(1998)臺灣產圓柏屬清水圓柏心材和臺灣刺柏葉部及根部之化學成分研究。國立臺灣大學化學研究所博士論文。325頁。
陳品方(2000)台灣杉與土肉桂精油及其成分之生物活性。國立臺灣大學森林學研究所碩士論文。65頁。
陳冠羲(2002)柳杉皮之化學成分研究。國立臺灣大學化學研究所碩士論文。101頁。
張東柱(1992)台灣阡插苗之兩種新病害。林業試驗所研究報告季刊 7:231-236。
張東柱(1993)三種土肉桂葉部新病害。林業試驗所研究報告季刊 8:51-59。
張東柱(1994)三椏白絹病及其病原菌存活。林業試驗所研究報告季刊 9:191-196。
張東柱(1995)台灣三種本土植物之輪斑病。林業試驗所研究報告季刊 10:235-240。
張東柱、謝煥儒、張瑞璋、傅春旭(1999)台灣常見樹木病害。林業試驗所。台北。6-139頁。
張瑞璋(1996)認識樹木病害及其防治方法。台灣省林業試驗所簡訊 3:1-4。
張豐吉、杜明宏(1993)台灣重要樹種化學性質之研究(VI)。中華林學季刊 6:113-125。
張上鎮、王升陽(1995)抗白蟻性木材抽出成分之探討。林產工業 14:149-159。
張上鎮、吳季玲、王升陽、蘇裕昌、郭悅雄(1998)臺灣杉心材抗菌性成分之研究 I. 正己烷可溶部抗菌成分之分離與鑑定。林產工業 17:287-304。
張上鎮、陳品方、張上淳(2000a)臺灣杉精油及抽出成分之抗細菌活性。中華林學季刊 33:123-129。
張上鎮、王升陽、吳季玲(2000b)臺灣杉木酚素之抗腫瘤潛力評估。中華林學季刊 33:277-282。
張惠婷、鄭森松、張上鎮、蘇裕昌、蔡坤憲、陳維鈞(2003)台灣肖楠葉部精油及其成分之抗病媒蚊活性。中華林學季刊 36:73-79。
鄭盈泓、張惠婷、張上鎮(2002)台灣肖楠葉部精油成分抑制林木病原真菌活性之評估。中華林學會91年森林學術論文發表會論文集。台中。13-21頁。
劉如芸(2006)六種化學品系土肉桂葉子精油抗細菌、腐朽菌、病媒蚊幼蟲及室塵蟎活性。國立臺灣大學森林環境暨資源學研究所碩士論文。79頁。
謝瑞忠、鍾森田、王守範(1986)省產杉木精油抗菌活性之研究。臺灣省林業試驗所研究報告第464號。5頁。
謝金霖(2004)台灣肖楠皮部之化學成分研究。國立臺灣大學化學研究所博士論文。353頁。
蘇文烱(1995)柳杉葉化學成份研究。國立臺灣大學化學研究所博士論文。442頁。
只木良也、吉良童夫(1983)ヒトと森林—森林の環境調節作用。共立出版株式會社。256頁。
慶松勝左衛門、石黑武雄、褔井儀五朗(1937)樹脂成分の研究(第十二報)—杉脂の結晶成分に就て。藥學雜誌 57:69-76。
Adams, R. P. (2001) Identification of essential oil components by gas chromatography/quadrupole mass spectroscopy. Allured, Illinois. 456 pp.
Aoyama, M. and S. Doi (1992) Antifungal activities of wood extractives of todomastu, Abies sachalinensis Masters, against pathogenic fungi causing turfgrass diseases. (in Japanese) Mokuzai Gakkaishi 38: 101-105.
Appleton, R. A., R. Mccrindle and K. H. Overton (1970) The diterpenes from the leaves of Cryptomeria japonica. Phytochemistry 23: 2062-2063.
Araujo, E. C. C., E. R. Silveira, M. A. S. Lima, M. A. Neto, I. L. D. Andrade and M. A. A. Lima (2003) Insecticidal activity and chemical composition of volatile oils from Hyptis martiusii Benth. J. Agric. Food Chem. 51: 3760-3762.
Arihara, S., A. Umeyama, S. Bando, S. Imoto, M. Ono, M. Tani and K. Yoshikawa (2004a) A new abietane and two dimeric abietane diterpenes from the black heartwood of Cryptomeria japonica. Chem. Pharm. Bull. 52: 354-358.
Arihara, S., A. Umeyama, S. Bando, S. Imoto, M. Ono and K. Yoshikawa (2004b) Three new sesquiterpenes from the black heartwood of Cryptomeria japonica. Chem. Pharm. Bull. 52: 463-465.
Ashitani, T., M. Ujike, S. Nagahama, T. Ueno and K. Sakai (2001) Characterization of sugi (Cryptomeria japonica) bark extracts. (in Japanese) Mokuzai Gakkaishi 47: 276-281.
Barrero, A. F., J. F. Sanchez, E. J. Alvarez-Manzaneda, M. M. Dorado and A. Haidour (1993) Terpenoids and sterols from the wood of Abies pinsapo. Phytochemistry 32: 1261-1265.
Bouchra, C., M. Achouri, L. M. I. Hassani and M. Hmamouchi (2003) Chemical composition and antifungal activity of essential oils of seven Moroccan Labiatae against Botrytis cinerea Pers: Fr. J. Ethnopharmacol. 89: 165-169.
Carpinella, M. C., L. M. Giorda, C. G. Ferrayoli and S. M. Palacios (2003) Antifungal effects of different organic extracts from Melia azedarach L. on phytopathogenic fungi and their isolated active components J. Agric. Food Chem. 51: 2506-2511.
Celimene, C. C., J. A. Micales, L. Ferge and R. A. Young (1999) Efficacy of pinosylvins against white-rot and brown-rot fungi. Holzforschung 53: 491-497.
Chang, S. T., S. Y. Wang, C. L. Wu, Y. C. Su and Y. H. Kuo (1999) Antifungal compounds in the ethyl acetate soluble fraction of the extractives of Taiwania (Taiwania cryptomerioides Hayata) heartwood. Holzforschung 53: 487-490.
Chang, S. T., S. Y. Wang, C. L. Wu, P. F. Chen and Y. H. Kuo (2000a) Comparison of the antifungal activity of cadinane skeletal sesquiterpenoids from Taiwania (Taiwania cryptomerioides Hayata) heartwood. Holzforschung 54: 241-245.
Chang, S. T., D. S. Y. Wang, C. L. Wu, S. G. Shiah, Y. H. Kuo and C. J. Chang (2000b) Cytotoxicity of extractives from Taiwania cryptomerioides heartwood. Phytochemistry 55: 227-232.
Chang, S. T., S. S. Cheng and S. Y. Wang (2001a) Antitermitic activity of essential oils and components from Taiwania (Taiwania cryptomerioides). J. Chem. Ecol. 27: 717-724.
Chang, S. T., P. F. Chen, S. Y. Wang and H. H. Wu (2001b) Antimite activity of essential oils and their constituents from Taiwania cryptomerioides. J. Med. Entomol. 38: 455-457.
Chang S. T. and S. S. Cheng (2002) Antitermite activity of leaf essential oils and their constituents from Cinnamomum osmophloeum. J. Agric. Food Chem. 50: 1389-1392.
Cheng, S. S., C. L. Wu, H. T. Chang, Y. T. Kao, and S. T.Chang (2004a). Antitermitic and antifungal activity of essential oil of Calocedrus formosana leaf and its composition. J. Chem. Ecol. 30: 1957-1967.
Cheng, S. S., J.Y. Liu, K. H. Tsai, W. J. Chen and S. T. Chang (2004b) Chemical composition and mosquito larvicidal activity of essential oils from leaves of different Cinnamomum osmophloeum provenances. J. Agric. Food Chem. 52: 4395-4400.
Cheng, S. S., J. Y. Liu, Y. R. Hsui and S. T. Chang (2006) Chemical polymorphism and antifungal activity of essential oils from leaves of different provenances of indigenous cinnamon (Cinnamomum osmophloeum). Bioresour. Technol. 97: 306-312.
Chilpa, R. R., F. G. Garibay, G. M. Torres, M. J. Estrada and R. I. Q. Vasquez (1998) Flavonoids and isoflavonoids with antifungal properties from Platymiscium yucatanum heartwood. Holzforschung 52: 459-462.
Ciccia, G., J. Coussio and E. Mongelli (2000) Insecticidal activity against Aedes aegypti larvae of some medicinal South American plants. J. Ethnopharmacol. 72: 185-189.
Danielsen, K. (1996) Anthraquinones by cyclisation of benzoylbenzoic acids produced by the AlCl3-mediated friedel-crafts reaction of phthalic anhydrides with aromatic compounds. Acta. Chem. Scand. 50: 954-957.
Dharmagadda, V. S. S., S. N. Naik, P. K. Mittal and P. Vasudevan (2005) Larvicidal activity of Tagetes patula essential oil against three mosquito species. Bioresour. Technol. 96: 1235-1240.
Dev, S. (1989) Terpenoids. pp.691-807. In J. W. Rowe ed. Natural Products of Woody Plants. Springer-Verlag Co., Berlin. 1242 pp.
Doi, S. and Y. Kurimoto (1998) Durability of sugi (Cryptomeria japonica D. Don) bark against wood decay fungi and a subterranean termite. Holz als Roh- und Werkstoff 56: 178.
Dudareva, N., S. Andersson, I. Orlova, N. Gatto, M. Reichelt, D. Rhodes, W. Boland and J. Gershenzon (2004) The nonmevalonate pathway supports both monoterpene and sesquiterpene formation in snapdragon flowers. Proc. Natl. Acad. Sci. U.S.A. 102: 933-938.
Eberhardt, T. L., J. S. Han, J. A. Micales and R. A. Young (1994) Decay resistance in conifer seed cones: Role of resin acids as inhibitors of decomposition by white-rot fungi. Holzforschung 48: 278-284.
Funaoka, K., Kuroda, Y., Y. Kai and T. Kondo (1963) On the phenolic constituents from Cryptomeria japonica D. Don. I. Isolation and a few characteristics of two phenolic substances. Mokuzai Gakkaishi 9: 139-141.
Gupta, K., K. S. Ayyar and R. Dayal (1987) Essential oil of indian Cryptomeria japonica. J. Indian. Chem. Soc. 64: 66-67.
Harborne, J. B. (1994) Phenolics. pp.361-388. In J. Mann et al. eds. Natural Products. Longman Scientific and Technical Co., New York. 472 pp.
Hart, J. H. (1989) The role of wood exudates and extractives in protecting wood from decay. pp.861-878. In J. W. Rowe, ed. Natural Products of Woody Plants. Springer-Verlag Co., Berlin. 1242 pp.
He, K., L. Zeng, G. Shi, G. X. Zhao, J. F. Kozlowski and J. L. McLaughlin (1997) Bioactive compounds from Taiwania cryptomerioides Hayata. J. Nat. Prod. 60: 38-40.
Ho, S. H., J. Wang, K. Y. Sim, G. C. L. Ee, Z. Imiyabir, K. F. Yap, K. Shaari and S. H. Goh (2003) Metliternatin: a feeding deterrent and larvicidal polyoxygenated flavone from Melicope subunifoliolata. Phytochemistry 62: 1121-1124.
Iijima, Y., R. Davidovid-Rikanati, E. Fridman, D. R. Gang, E. Bar, E. Lewinsohn and E. Pichersky (2004) The biochemical and molecular basis for the divergent patterns in the biosynthesis of terpenes and phenylpropenes in the peltate glands of three cultivars of basil. Plant Physiol. 136: 3724-3736.
Inamori, Y., Y. Sakagami, Y. Morita, M. Shibata, M. Sugiura, Y. Kumeda, T. Okabe, H. Tsujibo and N. Ishida (2000) Antifungal activity of hinokitiol-related compounds on wood-rotting fungi and their insecticidal activities. Biol. Pharm. Bull. 23: 995-997.
Ioset, J. R., A. Marston, M. P. Gupta and K. Hostettmann (2000a) Antifungal and larvicidal cordiaquinones from the roots of Cordia curassavica. Phytochemistry 53: 613-617.
Ioset, J. R., A. Marston, M. P. Gupta and K. Hostettmann (2000b) Antifungal and larvicidal compounds from the root bark of Cordia alliodora. J. Nat. Prod. 63: 424-426.
Ishikura, N., K. Nabeta and H. Sugisawa (1984) Volatile components in cell suspension cultures of Cryptomeria japonica. Phytochemistry 23: 2062-2063.
Islam, M. T., T. Ito, M. Sakasai and S. Tahara (2000) Zoosporicidal activity of polyflavonoid tannin identified in Lannea coromandelica stem bark against phytopathogenic oomycete Aphanomyces cochlioides. J. Agric. Food Chem. 50: 6697-6703.
Ito, S., M. Kodama, H. Nishiya and S. Narita (1969) Structure of cryptomerone, a bisabolane sesquiterpene from Cryptomeria japonica. Tetrahedron Letters 37: 3185-3186.
Ito, Y., Y. Hayashi and A. Kato (1995) Antifungal compounds from trees of genus Diospyros with complete assignment of nuclear magnetic resonance data. Mokuzai Gakkaishi 41: 694-698.
Itokawa, H., Y. Qiao and K. Takeya (1991) Anthraquinones, naphthoquinones and naphthohydroquinones from Rubia oncotricha. Phytochemistry 30: 637-640.
Jain, T. C. and C. M. Bank (1968) Phytochemical studies the structure of β–sitosterol. Can. J. Chem. 46: 2325-2328.
Kai, Y., H. Kuroda and F. Teratani (1972) On the phenolic constituents from Cryptomeria japonica D. Don. VI. Hydroxysugiresinol and coloration of heartwood. Mokuzai Gakkaishi 18: 315-321.
Kai, Y. (1991) Chemistry of extractives. pp.215-255. In D. N. S. Hon and N. Shiraish, eds. Wood and Cellulosic Chemistry. Marcell Dekker Inc., New York. 1019 pp.
Kalsi, P. S., G. S. Arora and R. S. Ghulati (1979) New antipodal sesquiterpene alcohols from vetiver oil. Phytochemistry 18: 1223-1224.
Kang, H. Y., N. Matsushima, K. Sameshima and N. Takamura (1990) Termite resistance tests of hardwoods of Kochi growth I. The strong termiticidal activity of kagonoki (Litsea coreana Léveillé). (in Japanese) Mokuzai Gakkaishi 36: 78-84.
Karmegam, N., M. Sakthivadivel, V. Anuradha and T. Daniel (1997) Indigenous-plant extracts as larvicidal agents against Culex quinquefasclatus say. Bioresour. Technol. 59: 137-140.
Kawamura, F., S. Ohara and A. Nishida (2004) Antifungal activity of constituents from the heartwood of Gmelina arborea: Part 1. Sensitive antifungal assay against basidiomycetes. Holzforschung 58: 189-192.
Kawano, N. (1960) Chemical constituents of the plants of coniferae and allied drders. XLVI. On the isolation of hinokiflavone from the leaves of Cryptomeria japonica D. Don. (in Japanese) J. Pharm. 80: 1647-1649.
Kim, M. K. G. J. Choi and H. S. Lee (2003) Fungicidal property of Curcuma longa L. rhizome-derived curcumin against phytopathogenic fungi in a greenhouse. J. Agric. Food Chem. 51: 1578-1581.
Kinjo, K., Y. Doufuku and S. Yaga (1988) Termiticidal substances from the wood of Chamaecyparis obtusa. Mokuzai Gakkaishi 34: 451-455.
Kishino, M., H. Ohi and A. Yamaguchi (1995) Characteristics of methanol extractives from Chengal wood and their antifungal properties. Mokuzai Gakkaishi 41: 444-447.
Kobayashi, K., C. Nishino, H. Tomita and M. Fukushima (1987) Antifungal activity of pisiferic acid derivatives against the rice blast fungus. Phytochemistry 26: 3175-3179.
Kofujita, H., Y. Fujino, T. Sasaki, M. Hasebe, M. Ota and K. Suzuki (2001) Antifungal activity of the bark of Cryptomeria japonica and its relevant components. (in Japanese) Mokuzai Gakkaishi 47: 479-486.
Kofujita, H., M. Ota, K. Takahashi, Y. Kawai and Y. Hayashi (2002) A diterpene quinone from the bark of Cryptomeria japonica. Phytochemistry 61: 895-898.
Kofujita, H., Y. Fujino, M. Ota and K. Takahashi (2006) Antifungal diterpenes from the bark of Cryptomeria japonica D. Don. Holzforschung 60: 20-23.
Kondo, T., H. Imamura and M. Suda (1959) Wood extractives part VIII. On the heartwood constituents of Cryptomeria japonica D. Don. Bull. Agric. Chem. Soc. Jpn. 23: 233-239.
Kondo, T., H. Imamura and M. Suda (1960) Wood extractives part IX. A new diterpene alcohol from Cryptomeria japonica D. Don. Bull. Agric. Chem. Soc. Jpn. 24: 65-68.
Kondo, R. and H. Imamura (1986) Antifungal compounds in heartwood extractives of hinoki (Chamaecyparis obtusa Endl.). (in Japanese) Mokuzai Gakkaishi 32: 213-217.
Kuo, Y. H., T. R. Wu, M. C. Cheng and Y. Wang (1990) Five new compounds from the heartwood of Juniperus formosana Hayata. Chem. Pharm. Bull. 38: 3195-3201.
Kuo, Y. H., C. F. Chyu and H. C. Lin (2003) Cadinane-type sesquiterpenes from the roots of Taiwania cryptomerioides Hayata. Chem. Pharm. Bull. 51: 986-989.
Kusuma, I. W., M. Azuma, T. Darma, K. Itoh and S. Tachibana (2005) Isolation and identification of antifungal compounds from Amboyna wood. Holzforschung 59: 170-172.
Lee, H. C., S. S. Cheng and S. T. Chang (2005) Antifungal property of the essential oils and their constituents from Cinnamon osmophloeum leaf against tree pathogenic fungi. J. Sci. Food Agric. 85: 2047-2053.
Li, E., A. M. Clark and C. D. Hufford (1995) Antifungal evaluation of pseudolaeric acid B, a major constituent of Pseudolarix kaempferi. J. Nat. Prod. 58: 57-67.
Lin, Y. T., Y. H. Kuo and B. H. Chang (1975) Studies on the extractive constituents of the bark of Libocedrus formosana florin. II. J. Chin. Chem. Soc. 22: 331-334.
Matsunaga, T., C. Hasegawa, T. Kawasuji, H. Suzuki, H. Saito, T. Sagioka, R. Takahashi, H. Tsukamoto, T. Morikawa and T. Akiyama (2000) Isolation of the antiulcer compound in essential oil from the leaves of Cryptomeria japonica. Biol. Pharm. Bull. 23: 595-598.
Meyer, B. N., N. R. Ferrigni, J. E. Putnam, L. B. Jascobsen, D. E. Nichols and J. L. McLaughlin (1982) Brine shrimp: A convenient general bioassay for active plant constituents. Planta Medica 45: 31-34.
Miura, H., N. Kawano and J. A. C. Waiss (1966) Cryptomerin A and B, hinokiflavone methyl ethers from the leaves of Cryptomeria japonica. Chem. Pharm. Bull. 14: 1404-1408.
Mori, M., M. Aoyama and S. Doi (2000) Antifungal constituents in the bark of Magnolia obovata Thunb.. J. Hokkaido For. Prod. Res. Inst. 14(1): 1-5.
Morita, S., M. Yatagai and T. Ohira (1991) Antimite and antifungi activities of the hexane extractives from yakusugi bogwood. (in Japanese) Mokuzai Gakkaishi 37: 352-357.
Morita, S. and M. Yatagai (1994) Antimite components of the hexane extractives from domaiboku yakusugi (Cryptomeria japonica). (in Japanese) Mokuzai Gakkaishi 40: 996-1002.
Morita, S., T. Hidaka and M. Yatagai (1997) Antifungal compounds of the extractives of yakusugi (Crypromeria japonica D. Don). (in Japanese) Wood Preservation 23: 11-19.
Nagahama, S. (1964) Terpenoids. VIII. Sesquiterpenoids from the wood oil of 'sugi' (Cryptomeria japonica D. Don). Bull. Chem. Soc. Jpn. 37: 1029-1033.
Nagahama, S. and M. Tazaki (1993) Terpenoids of wood oil of sugi (Cryptomeria japonica) peculiarities of obisugi variety. (in Japanese) Mokuzai Gakkaishi 39: 1077-1083.
Nagahama, S., M. Tazaki, H. Kobayashi and M. Sumimoto (1993) Sesquiterpene alcohols from Cryptomeria japonica and C. fortunei leaf oil. Phytochemistry 33: 879-882.
Nagahama, S., M. Tazaki, K. Nishimura and M. Tajima (1994) ent-Rosa-5,15-diene, a diterpene hydrocarbon in Cryptomeria leaf oil. Phytochemistry 36: 77-78.
Nagahama, S., M. Tazaki, H. Nomura, K. Nishimura and M. Tajima (1995) Terpenoids of the wood oil of sugi (Cryptomeria japonica) II. Components of same clone from different habitats. (in Japanese) Mokuzai Gakkaishi 42: 330-333.
Nagahama, S., M. Tazaki, T. Sanetika, H. Nomura, K. Nishimura and M. Tajima (1996a) Terpenoids of the wood oil of sugi (Cryptomeria japonica) III. Components of yakusugi. (in Japanese) Mokuzai Gakkaishi 42: 1121-1126.
Nagahama, S., M. Tazaki, H. Nomura, K. Nishimura, M. Tajima and Y. Iwasita (1996b) Terpenoids of the wood oil of sugi (Cryptomeria japonica) IV. Components of yabukuguri. (in Japanese) Mokuzai Gakkaishi 42: 1127-1133.
Nagahama, S., M. Tazaki, T. Sanetika, K. Nishimura and M. Tajima (1998) Terpenoids of the wood oil of sugi (Cryptomeria japonica) V. Components of form. ayasugi. (in Japanese) Mokuzai Gakkaishi 44: 282-286.
Nagahama, S., T. Iwaoka and T. Ashitani (2000) Terpenoids of the wood oil of sugi (Cryptomeria japonica) VI. Components of elite clones kenkuma-3, kenkoyu-3 and kenaira-14. (in Japanese) Mokuzai Gakkaishi 46: 225-230.
Nagahama, S., T. Tukamoto, N. Torii, T. Sonoda and T. Yamanobe (2001) Terpenoids of the wood oil of sugi (Cryptomeria japonica) VII. Components of elite clones minamatasho-4, and five others. (in Japanese) Mokuzai Gakkaishi 47: 487-492.
Nagahama, S., H. Fujii, T. Sonoda and M. Sasaki (2002) Terpenoids of the wood oil of sugi (Cryptomeria japonica) VIII. Components of kenkunisaki-5 and five others elite clones. (in Japanese) Mokuzai Gakkaishi 48: 380-386.
Nakajima, K., T. Yoshimoto and T. Fukuzumi (1980) Substance inhibiting growth of shiitaka mycelium in sugi wood (Cryptomeria japonica D. Don). Mokuzai Gakkaishi 26: 698-702.
Nakatsuka, T., Y. Hirose and M. Matsuda (1957) Terpenoids II. Composition of the essential oil from the leaves of 'sugi' (Cryptomeria japonica D. Don). Mokuzai Gakkaishi 3: 206-208.
Nishida, T., Y. Hanamura and Y. Tsutsumi (1995) Superoxide dismutase mimic and tyrosinase inhibitory activities of extractives from sugi (Cryptomeria japonica). Mokuzai Gakkaishi 41: 522-524.
Ogata, H. and K. Ogiyama (2000) Chemical compositions and antipathogenic activities of constituent fatty acids from neutral wax in foliage of Cryptomeria japonica. (in Japanese) Mokuzai Gakkaishi 46: 54-62.
Ohashi, H., S. Kawai, Y. Sakurai and M. Yasue (1992) Norlignan from the knot resin of Araucaria angustifolia. Phytochemistry 31: 1371-1373.
Ohashi, H., T. Asai and S. Kawai (1994) Screening of main Japanese conifers for antifungal leaf components, sesquiterpenes of Juniperus chinesis var. pyramidalis. Holzforschung 48: 193-198.
Ohira, T. and M. Yatagai (1993) Extractives of Abies mariesii Masters II. Mokuzai Gakkaishi 39: 237-242.
Ohtani, Y., M. Hazama and K. Sameshima (1997) Crucial chemical factors of the termiticidal activity of hinoki wood (Chamaecyparis obtusa) III. Contribution of α-terpinyl acetate to the termiticidal activity of hinoki wood. (in Japanese) Mokuzai Gakkaishi 43: 1022-1029.
Pilotti, C. A., R. Kondo, K. Shimizu and K. Sakai (1995) An examination of the anti-fungal components in the heartwood extracts of Pterocarpus indicus. Mokuzai Gakkaishi 41: 593-597.
Pitarokili, D., M. Couladis, N. P. Panayotarou and O. Tzakou (2002) Composition and antifungal activity on soil-borne pathogens of the essential oil of Salvia sclarea from Greece. J. Agric. Food Chem. 50: 6688-6691.
Pitarokili, D., O. Tzakou, A. Loukis and C. Harvala (2003) Volatile metabolites from Salvia fruticosa as antifungal agents in soilborne pathogens. J. Agric. Food Chem. 51: 3294-3301.
Rahuman, A. A., G. Gopalakrishnanb, B. S. Ghousea, S. Arumugama and B. Himalayana (2000) Effect of Feronia limonia on mosquito larvae. Fitoterapia 71: 553-555.
Ramsewak, R., M. G. Nair, S. Murugesan, W. J. Mattson and J. Zasada (2001) Insecticidal fatty acids and triglycerides from Dirca palustris. J. Agric. Food Chem. 49: 5852-5856.
Saeki, I., M. Suminoto and T. Kondo (1973) The termiticidal substances from the wood of Chamaecyparis pisifera D. Don. Holzforschung 27: 93-96.
Sakthivadivel, M. and D. Thilagavathy (2003) Larvicidal and chemosterilant activity of the acetone fraction of petroleum ether extract from Argemone mexicana L. seed. Bioresour. Technol. 89: 213-216.
Samejima, M. and T. Yoshimoto (1979) Procyandins from the inner bark of sugi (Cryptomeria japonica D. Don). Mokuzai Gakkaishi 25: 671-677.
Schultz, T. P., W. B. Harms, T. H. Fisher, K. D. McMurtrey, J. Minn and D. D. Nicholas (1995) Durability of angiosperm heartwood: The importance of extractives. Holzforschung 49: 29-34.
Shibuya, T. (1992) Cryptoquinonemethides D and E, C30-terpene quinone methides, from Cryptomeria japonica. Phytochemistry 31: 4289-4294.
Shieh, B., Y. Iizuka and Y. Matsubara (1981) Monoterpenoid and sesquiterpenoid constituents of the essential oil of sugi (Cryptomeria japonica D. Don.). Agric. Biol. Chem. 45: 1493-1495.
Shieh, J. C. and M. Sumimoto (1992) Antifungal wood component of Cunninghamia lanceolata. Mokuzai Gakkaishi 38: 482-489.
Shimizu, M., H. Tsuji, H. Shogawa, H. Fukumura, S. Tanaami, T. Wayashi, M. Arisawa and N. Morita (1988) Anti-inflammatory constituents of topically applied crude drugs. II. Constituents and anti-inflammatory effect of Cryptomeria japonica D. Don. Chem. Pharm. Bull. 36: 3967-3973.
Siddiqui, B. S., F. Afshan, Ghiasuddin, S. Faizi, S. N. H. Naqvi and R. M. Tariq (2000) Two insecticidal tetranortriterpenoids from the fresh fruit coats of Azadirachta indica. Phytochemistry 53: 371-376.
Singh, G., O. P. Singh, Y. R. Prasad, M. P. de Lampasona and C. Catalan (2002) Studies on essential oils, Part 33: chemical and insecticidal investigations on leaf oil of Coleus amboinicus Lour. Flavour Fragr. J. 17: 440-442.
Singh, G., O. P. Singh, M. P. de Lampasona and C. A. N. Catalan (2003) Studies on essential oils. Part 35: chemical and biocidal investigations on Tagetes erecta leaf volatile oil. Flavour Fragr. J. 18: 62-65.
Sogabe, A., K. Kinjo, F. Abe, T. Yamauchi and S. Yaga (2000a) Termiticidal substances from the wood and bark of Wikstroemia retusa A. Gray. (in Japanese) Mokuzai Gakkaishi 46: 47-53.
Sogabe, A., K. Kinjo, F. Abe, T. Yamauchi and S. Yaga (2000b) Termiticidal substances from the heartwood of Cryptomeria japonica D. Don. (in Japanese) Mokuzai Gakkaishi 46: 124-131.
Su, W. C., J. M. Fang and Y. S. Cheng (1993) Hexacarbocyclic triterpenes from leaves of Cryptomeria japonica. Phytochemistry 34: 779-782.
Su, W. C., J. M. Fang and Y. S. Cheng (1994a) Abietanes and kauranes from leaves of Cryptomeria japonica. Phytochemistry 35: 1279-1284.
Su, W. C., J. M. Fang and Y. S. Cheng (1994b) Labdanes from leaves of Cryptomeria japonica. Phytochemistry 37: 1109-1114.
Su, W. C., J. M. Fang and Y. S. Cheng (1995a) Synthesis and structure determination of cryptomanhydride, an uncommon natural terpenic anhydride. Tetrahedron Letters 36: 5367-5370.
Su, W. C., J. M. Fang and Y. S. Cheng (1995b) Sesquiterpenes from leaves of Cryptomeria japonica. Phytochemistry 39: 603-607.
Su, W. C., J. M. Fang and Y. S. Cheng (1995c) Flavonoids and lignans from leaves of Cryptomeria japonica. Phytochemistry 40: 563-566.
Su, W. C., J. M. Fang and Y. S. Cheng (1996) Diterpenoids from leaves of Cryptomeria japonica. Phytochemistry 41: 255-261.
Takahashi, K. (1981) Heartwood phenols and their significance to color in Cryptomeria japonica D. Don. Mokuzai Gakkaishi 27: 654-657.
Takahashi, K., M. Yasue and K. Ogiyama (1983) Phenols of 'Tabigusare' wood discolored sugi (Cryptomeria japonica) sapwood. Mokuzai Gakkaishi 29: 806-809.
Takahashi, K. and K. Ogiyama (1985) Phenols of discolored sugi (Cryptomeria japonica) sapwood. III. Norlignans of ayasugi (cultivar) in the Kyushu region. Mokuzai Gakkaishi 32: 457- 461.
Takahashi, K., M. Yasue and K. Ogiyama (1988) A norlignan cryptoresinl from the heartwood of Cryptomeria japonica. Phytochemistry 27: 1550-1552.
Tatsuya, A., T. Iwaoka and S. Nagahama (1999) 11α-Hydroxy-7,13-abietadiene from sugi (Cryptomeria japonica) wood extract. Nat. Prod. Lett. 13: 169-170.
Taylor, W. G., T. W. Hall and D. D. Vedres (1998) Synthesis and larvicidal properties of some cyclopropylcarboxamides related to cis-permetherin. J. Agric. Food Chem. 46: 1572-1576.
Uchida, S. (1916) The essential oil of sugi (Cryptomeria japonica) leaves. J. Am. Chem. Soc. 38: 687-698.
Uchida, S. and J. Murata (1937) The essential oil of sugi (Cryptomeria japonica). J. Soc. Chem. Ind. 450: 310.
Wang, S. Y., J. H. Wu, L. F. Shyur, Y. H. Kuo and S. T. Chang (2002) Antioxidant activity of abietane-type diterpenes from heartwood of Taiwania cryptomerioides Hayata. Holzforschung 56: 487-492.
Wang, S. Y., P. F. Chen and S. T. Chang (2005) Antifungal activities of essential oils and their constituents from indigenous cinnamon (Cinnamomum osmophloeum) leaves against wood decay fungi. Bioresour. Technol. 96: 813-818.
Wang, S. Y., C. L. Wu, F. H. Chu, S. C. Chien, Y. H. Kuo, L. F. Shyur and S. T. Chang (2005) Chemical composition and antifungal activity of essential oil isolated from Chamaecyparis formosensis (Matsun) wood. Holzforschung. 59: 295-299.
Wenkert, E. and B. L. Bucjwalter (1972) Carbon-13 nuclear magnetic resonance spectroscopy of naturally occurring substances. J. Am. Chem. Soc. 94(12): 4367-4369.
Yaga, S. (1970) On the termite-resistance of Okinawan timbers I. Method of bioassay and effect of wood extractives on the termite-resistance. (in Japanese) Mokuzai Gakkaishi 21: 113-119.
Yaga, S. (1977) On the termite-resistance of Okinawan timbers IV. The termiticidal substances from the wood and bark of Adina racemosa Miq. (in Japanese) Mokuzai Gakkaishi 23: 594-600.
Yaga, S. (1980) On the termite-resistance of Okinawan timbers VI. Termiticidal substances from Melia azedarach L. (in Japanese) Mokuzai Gakkaishi 26: 494-498.
Yaga, S. and K. Kinjo (1985) On the termite-resistance of Okinawan timbers IX. Termiticidal substances from the wood of Guettarda speciosa L. (in Japanese) Mokuzai Gakkaishi 31: 684-687.
Yaga, S., K. Kinjo, E. C. Fernzndez, J. V. Zerrudo and S. A. Castillo (1991) On the termite-resistance of Okinawan timbers X. Termiticidal substances from Bruguiera gymnorrhiza. (in Japanese) Mokuzai Gakkaishi 37: 358-362.
Yamada, T., H. Tamura and K. Mineo (1988) The response of sugi (Cryptomeria japonica D. Don) sapwood to fungal invasion following attack by the sugi bark borer. Physiol. Mol. Plant Pathol. 33: 429-442.
Yang, Y. C., S. G. Lee, H. K. Lee, M. K. Kim, S. H. Lee and H. S. Lee (2002) A piperidine amide extracted from Piper longum L. fruit shows activity against Aedes aegypti mosquito larvae. J. Agric. Food Chem. 50: 3765-3767.
Yang, Y. C., M. Y. Lim and H. S. Lee (2003) Emodin isolated from Cassia obtusifolia seed shows larvicidal activity against three mosquito species. J. Agric. Food Chem. 51: 7629-7631.
Yatagai, M., Y. Miyazaki and T. Ohira (1991) Extractives from yakusugi bogwood and their termicidal activity and growth regulation effects on plant seeds. (in Japanese) Mokuzai Gakkaishi 37: 352-357.
Yatagai, M., H. Makihara and K. Oba (2002) Volatile components of Japanese cedar cultivars as repellents related to resistance to Cryptomeria bark borer. J. Wood Sci. 48: 51-55.
dc.identifier.urihttp://tdr.lib.ntu.edu.tw/jspui/handle/123456789/33937-
dc.description.abstract柳杉(Cryptomeria japonica D. Don, Japanese cedar)為台灣重要造林樹種之一,如何利用此一資源已成為當前林業經營與林產利用的重要課題。因此,本研究分別以水和甲醇萃取柳杉各部位精油及抽出成分,進行生物活性之篩選,嘗試分離及純化柳杉中具抗木材腐朽菌、抗植物病原菌、抗白蟻和抗病媒蚊幼蟲等生物活性之主要成分。所得之純化合物則利用質譜、紅外線光譜及核磁共振光譜等儀器分析鑑定其化學結構,同時亦將純化合物進行各項試驗以確認其生物活性;另外,亦探討抽出成分結構與生物活性之相關性。
由氣相層析儀和氣相層析-質譜儀分析結果得知,心材精油主成分為γ-Cadinene(14.46%)、epi-Bicyclosesquiphellandrene(13.15%)及δ-Cadinene(12.86%);邊材精油主成分為Isopimarol(23.11%)、Ferruginol(14.74%);樹皮精油主成分為Ferruginol(16.81%)和δ-Cadinene(6.76%);葉子精油主成分為ent-Kaur-16-ene(24.90%)和β-Elemol(18.84%)。又本研究由柳杉心材、邊材、葉子和樹皮中共分離出24種化合物,包括Bisabola-7(14),10- dien-1α,4α-diol、Khusinodiol、δ-Cadinol、α-Cadinol、γ-Eudesmol、β-Eudesmol、β-Elemol、Cryptomeridol、Ferruginol、Cryptojaponol、Isopimaric acid、7β-Hydroxydeoxocryptojaponol、Isopimarol、Isopimarinol、Phyllocladan-16α-ol、Sandaracopimaric acid、12-Hydroxy-6,7-secoabieta-8,11,13-trien-6,7-dial、ent-Kaur-16-ene、Sugiol、Cryptoresinol、2-Methylanthraquinone、6β,22- Dihydroxystigmasterol、(22S)-5α-Ergostane-3α,22-diol及β-Sitosterol。其中,Khusinodiol、2-Methylanthraquinone、6β,22-Dihydroxy-stigmasterol和(22S)-5α- Ergostane-3α,22-diol是首次從柳杉中分離得到。
由抗菌試驗結果得知,心材精油HO4分離部之所以具較佳的抗腐朽菌和抗植物病原菌活性,與β-Eudesmol、β-Elemol、δ-Cadinol和Ferruginol 四種化合物有關。由抗台灣家白蟻試驗結果顯示,柳杉葉子精油和甲醇抽出物均具有很強的抗白蟻活性,而葉子精油之作用機制係由揮發性和接觸毒二者共同作用而造成。比較各化合物之抗白蟻活性,證實β-Eudesmol、p-Cymene、Terpinene-4-ol、α-Terpineol、α-Pinene和γ-Terpinene 四種化合物對台灣家白蟻均有很好的毒殺效果。
由抗病媒蚊幼蟲試驗結果得知,柳杉葉子精油之LO2分離部和邊材甲醇抽出物之正已烷可溶部對埃及斑蚊幼蟲和白線斑蚊幼蟲均有很好的抑制效果。比較抽出成分之抗病媒蚊幼蟲活性,以邊材正己烷可溶部SH3分離部得到2-Methylanthraquinone和葉子精油中LO2分離部所得到Limonene、γ-Terpinene、Terpinolene、β-Myrcene、3-Carene、p-Cymene 六種化合物對埃及斑蚊和白線斑蚊幼蟲均具有很好的抑制效果,其中,2-Methylanthraquinone對二種病媒蚊幼蟲之毒殺效果最強,其效果幾可媲美商業用的陶斯松。進一步比較2-Methylanthraquinone衍生物之抗病媒蚊幼蟲活性,仍然以C-2位置上接甲基(-CH3)之2-Methylanthraquinone毒殺效果最佳。而由海蝦致死試驗結果得知,柳杉葉子精油和Limonene、γ-Terpinene、Terpinolene、β-Myrcene、3-Carene及p-Cymene 六種化合物對海蝦都有毒殺效果,顯示葉子精油和6種化合物若要作為天然殺孑孓藥劑,並不適合應用於有其他生物的水中。至於柳杉邊材甲醇抽出物及2-Methylanthraquinone對海蝦之LC50值分別大於100 μg/mL和大於50 μg/mL,顯示二者對海蝦並沒有毒性,適合開發成理想的天然殺孑孓藥劑。
zh_TW
dc.description.abstractThe Japanese cedar, Cryptomeria japonica D. Don, is well-known in Taiwan as one of the important plantation tree species, thereby the potential utilizations of C. japonica are imperative study for forest management and wood production. Thus, in this study the essential oils and extracts from different parts of C. japonica were extracted with hot water and methanol, respectively, and followed by evaluating their bioactivities using various kinds of assays, including antifungal, antipathogenic, antitermitic, and mosquito larvicidal bioactivities. The pure compounds of essential oils and methanolic extracts of C. japonica were finally isolated by chromatographic separation techniques and identified by modern spectroscopic analyses, such as MS, FTIR, NMR, etc. Identified compounds were also examined with bioactive assays to confirm their bioactivities. In addition, the structure-bioactivity relationships of extractives were also elucidated.
From the results of GC and GC-MS analyses, the heartwood essential oil was found to contain mainly γ-cadinene (14.46%), epi-bicyclosesqui- phellandrene (13.15%) and δ-cadinene (12.86%); the main constituents of sapwood essential oil were isopimarol (23.11%) and ferruginol (14.74%); the bark essential oil has ferruginol (16.81%) and δ-cadinene (6.76%) as main compounds and ent-kaur-16-ene (24.90%) and β-elemol (18.84%) were the dominant components of leaf essential oil. In addition, twenty-four compounds were isolated and identified from the heartwood, sapwood, bark and leaf of C. japonica, including bisabola-7(14),10-dien-1α,4α-diol, khusinodiol, δ-cadinol, α-cadinol, γ-eudesmol, β-eudesmol, β-elemol, cryptomeridol, ferruginol, cryptojaponol, isopimaric acid, 7β-hydroxydeoxocryptojaponol, isopimarol, isopimarinol, phyllocladan-16α-ol, sandaracopimaric acid, 12-hydroxy-6,7- secoabieta-8,11,13-trien-6,7-dial, ent-kaur-16-ene, sugiol, cryptoresinol, 2-methylanthraquinone, 6β,22-dihydroxystigmasterol, (22S)-5α-ergostane- 3α,22-diol and β-sitosterol. Among them, khusinodiol, 2-methylanthraquinone, 6β,22-dihydroxystigmasterol and (22S)-5α-ergostane-3α,22-diol were first isolated from C. japonica.
From the results of antifungal assay, the HO4 fraction of heartwood essential oil had the strongest antifungal activity against four wood decay fungi and six plant pathogenic fungi. It correlates with the presence of β-eudesmol, β-elemol, δ-cadinol and ferruginol. On the basis of the results of antitermitic activity against Coptotermes formosanus Shiraki, the essential oil and methanolic extract from C. japonica leaf had the strongest termiticidal property. The termiticidal mechanisms of leaf essential oil are attributable to its volatility and toxicity. Comparison of antitermitic activity of eleven compounds revealed that β-eudesmol, p-cymene, terpinene-4-ol, α-terpineol, α-pinene and γ-terpinene showed high antitermitic activities.
Results obtained from the mosquito larvicidal tests, the LO2 fraction of leaf essential oil and Hex. sol. fraction of sapwood extract were found to be the most effective against both Aedes aegypti and Aedes albopictus larvae. Comparison of mosquito larvicidal activity of thirteen compounds revealed that 2-methylanthraquinone isolated from SH3 fraction and limonene, γ-terpinene, terpinolene, β-myrcene, 3-carene and p-cymene isolated from LO2 fraction had the best inhibitory effect against A. aegypti and A. albopictus larvae. Among these pure constituents, 2-methylanthraquinone exhibited the best mosquito larvicidal action against A. aegypti and A. albopictus larvae. The mosquito larvicidal activity of 2-methylanthraquinone was similar to that of chlorpyrifos, which is a well-known commercial insecticide. In addition, comparisons of mosquito larvicidal activity of 2-methylanthraquinone congeners demonstrated that anthraquinone skeletaton with a methyl group at C-2, such as 2-methylanthraquinone, exhibited the strongest mosquito larvicidal activity.
Based on the results of the brine shrimp toxicity assay, leaf essential oil, limonene, γ-terpinene, terpinolene, β-myrcene, 3-carene and p-cymene were demonstrated to have a high toxicity against the brine shrimp, indicating they may be toxic to other invertebrates in the river. In addition, sapwood methanolic extract and 2-methylanthraquinone tested showed a low toxicity against the brine shrimp, with a LC50 >100 μg/mL and >50 μg/mL, respectively, indicating they have good potential as a source for natural larvicides.
en
dc.description.provenanceMade available in DSpace on 2021-06-13T05:49:29Z (GMT). No. of bitstreams: 1
ntu-95-D89625006-1.pdf: 3543212 bytes, checksum: 1c153d10e19a886bb95687ab95d40fc8 (MD5)
Previous issue date: 2006
en
dc.description.tableofcontents目錄 …………………………………………………………………………… I
表目次 ………………………………………………………………………… V
圖目次 ………………………………………………………………………… IX
摘要 …………………………………………………………………………… 1
Abstract ……………………………………………………………………….. 3
壹、緒言 ……………………………………………………………………… 6
貳、文獻回顧 ………………………………………………………………… 9
一、木材抽出成分之抗腐朽菌活性 ………………………………………… 9
二、木材抽出成分之抗植物病原菌活性 …………………………………… 11
三、木材抽出成分之抗白蟻活性 …………………………………………… 13
四、木材抽出成分之抗病媒蚊幼蟲活性 …………………………………… 15
五、柳杉抽出成分之研究 …………………………………………………… 16
(一)聚酚類 ………………………………………………………………… 17
1. 木酚素 …………………………………………………………………... 17
2. 類木酚素 ………………………………………………………………... 19
3. 黃酮類 …………………………………………………………………... 19
(二)萜類 …………………………………………………………………… 20
1. 單萜類 …………………………………………………………………... 22
2. 倍半萜類 ………………………………………………………………... 23
3. 二萜類 …………………………………………………………………... 28
4. 三萜類 …………………………………………………………………... 34
(三)其他化合物 …………………………………………………………… 35
六、柳杉抽出成分之生物活性 ……………………………………………… 36
(一)抗真菌活性 …………………………………………………………… 36
(二)抗植物病原菌活性 …………………………………………………… 37
(三)抗蟲活性 ……………………………………………………………… 37
(四)抗蟎活性 ……………………………………………………………… 37
(五)抗發炎和抗氧化活性 ………………………………………………… 38
參、材料與方法 ……………………………………………………………… 39
一、試驗材料 ………………………………………………………………… 39
(一)柳杉 …………………………………………………………………… 39
(二)試驗菌株 ……………………………………………………………… 39
1. 木材腐朽菌 …………………………………………………………….. 39
2. 植物病原菌 …………………………………………………………….. 39
(三)培養基 ………………………………………………………………… 40
(四)白蟻 …………………………………………………………………… 40
(五)病媒蚊 ………………………………………………………………… 40
(六)藥品 …………………………………………………………………… 40
1. 試藥 …………………………………………………………………….. 40
2. 標準品 ………………………………………………………………….. 40
二、試驗方法 ………………………………………………………………… 41
(一)各部位精油之萃取 …………………………………………………… 41
(二)各部位精油成分及含量之鑑定 ……………………………………… 41
1. 氣相層析分析 ………………………………………………………….. 41
2. 氣相層析-質譜分析 ……………………………………………………. 42
(三)各部位抽出物之萃取與初步分離 …………………………………… 42
(四)抽出成分之分離與純化 ……………………………………………… 44
(五)化合物結構鑑定 ……………………………………………………… 44
(六)抗真菌試驗 …………………………………………………………… 45
(七)抗白蟻試驗 …………………………………………………………… 46
(八)抗病媒蚊幼蟲試驗 …………………………………………………… 47
(九)海蝦致死試驗 ………………………………………………………… 48
(十)統計分析 ……………………………………………………………… 48
肆、結果與討論 ……………………………………………………………… 49
一、柳杉各部位精油之含量 ………………………………………………… 49
二、柳杉各部位精油成分分析 ……………………………………………… 49
三、柳杉各部位抽出物與各可溶部之收率 ………………………………… 55
四、柳杉抽出成分之分離與鑑定 …………………………………………… 56
(一)化合物S1之分離與鑑定 ……………………………………………. 59
(二)化合物S2之分離與鑑定 ……………………………………………. 63
(三)化合物S3之分離與鑑定 ……………………………………………. 66
(四)化合物S4之分離與鑑定 ……………………………………………. 68
(五)化合物S5之分離與鑑定 ……………………………………………. 70
(六)化合物S6之分離與鑑定 ……………………………………………. 72
(七)化合物S7之分離與鑑定 ……………………………………………. 74
(八)化合物S8之分離與鑑定 ……………………………………………. 76
(九)化合物D1之分離與鑑定 ……………………………………………. 78
(十)化合物D2之分離與鑑定 ……………………………………………. 80
(十一)化合物D3之分離與鑑定 …………………………………………. 81
(十二)化合物D4之分離與鑑定 …………………………………………. 84
(十三)化合物D5之分離與鑑定 …………………………………………. 86
(十四)化合物D6之分離與鑑定 …………………………………………. 88
(十五)化合物D7之分離與鑑定 …………………………………………. 89
(十六)化合物D8之分離與鑑定 …………………………………………. 92
(十七)化合物D9之分離與鑑定 …………………………………………. 94
(十八)化合物D10之分離與鑑定 ……………………………………….. 96
(十九)化合物D11之分離與鑑定 ………………………………………… 100
(二十)化合物NL1之分離與鑑定 ………………………………………… 102
(二十一)化合物AQ1之分離與鑑定 ……………………………………... 106
(二十二)化合物ST1之分離與鑑定 ……………………………………… 111
(二十三)化合物ST2之分離與鑑定 ……………………………………… 113
(二十四)化合物ST3之分離與鑑定 ……………………………………… 115

五、抗木材腐朽菌活性 ……………………………………………………… 117
(一)柳杉各部位精油之抗木材腐朽菌活性 ……………………………… 117
(二)柳杉各部位甲醇抽出物之抗木材腐朽菌活性 ……………………… 122
(三)柳杉抽出成分之抗木材腐朽菌活性 ………………………………… 124
六、抗植物病原菌活性 ……………………………………………………… 126
(一)柳杉各部位精油之抗植物病原菌活性 ……………………………… 126
(二)柳杉各部位甲醇抽出物之抗植物病原菌活性 ……………………… 130
(三)柳杉抽出成分之抗植物病原菌活性 ………………………………… 132
七、抗白蟻活性 ……………………………………………………………… 134
(一)柳杉各部位精油之抗白蟻活性 ……………………………………… 134
(二)柳杉各部位精油抗白蟻的作用機制 ………………………………… 141
(三)柳杉各部位甲醇抽出物之抗白蟻活性 ……………………………… 144
(四)柳杉抽出成分之抗白蟻活性 ………………………………………… 145
八、抗病媒蚊幼蟲活性 ……………………………………………………… 148
(一)柳杉各部位精油之抗病媒蚊幼蟲活性 ……………………………… 148
(二)柳杉各部位甲醇抽出物之抗病媒蚊幼蟲活性 ……………………… 156
(三)柳杉抽出成分之抗病媒蚊幼蟲活性 ………………………………… 162
1. 13種化合物之抗病媒蚊幼蟲活性 ……………………………………... 162
2. 2-Methylanthraquinone衍生物之抗病媒蚊幼蟲活性 ……………….. 166
九、海蝦致死試驗評估 ……………………………………………………… 170
(一)柳杉各部位精油之海蝦致死試驗評估 ……………………………… 170
(二)柳杉各部位甲醇抽出物之海蝦致死試驗評估 ……………………… 171
(三)柳杉抽出成分之海蝦致死試驗評估 ………………………………… 173
伍、結論與建議 ……………………………………………………………… 175
陸、參考文獻 ………………………………………………………………… 178
柒、附錄一 柳杉4部位精油組成分結構式 ……………………………….. 195
捌、附錄二 博士班修業期間之研究成果(2000-2006) ………………… 199
dc.language.isozh-TW
dc.subject精油zh_TW
dc.subject海蝦致死試驗zh_TW
dc.subject抗病媒蚊幼蟲活性zh_TW
dc.subject抗白蟻活性zh_TW
dc.subject抗植物病原菌活性zh_TW
dc.subject抗木材腐朽菌活性zh_TW
dc.subject柳杉zh_TW
dc.subject抽出成分zh_TW
dc.subjectessential oilen
dc.subjectantipathogenic activityen
dc.subjectantifungal activityen
dc.subjectextractivesen
dc.subjectCryptomeria japonicaen
dc.subjectbrine shrimp toxicity assayen
dc.subjectmosquito larvicidal activityen
dc.title柳杉抗真菌及抗蟲成分之分析與鑑定zh_TW
dc.titleAnalyses and Identification of Antifungal and Insecticidal Compounds from Cryptomeria japonicaen
dc.typeThesis
dc.date.schoolyear94-2
dc.description.degree博士
dc.contributor.oralexamcommittee王松永(Song-Yung Wang),郭悅雄(Yueh-Hsiung Kuo),劉正字(Cheng-Tzu Liu),蘇裕昌(Yu-Chang Su),林正榮(Cheng-Jung Lin),陳維鈞(Wei-June Chen),王升陽(Sheng-Yang Wang)
dc.subject.keyword柳杉,精油,抽出成分,抗木材腐朽菌活性,抗植物病原菌活性,抗白蟻活性,抗病媒蚊幼蟲活性,海蝦致死試驗,zh_TW
dc.subject.keywordCryptomeria japonica,essential oil,extractives,antifungal activity,antipathogenic activity,mosquito larvicidal activity,brine shrimp toxicity assay,en
dc.relation.page204
dc.rights.note有償授權
dc.date.accepted2006-07-10
dc.contributor.author-college生物資源暨農學院zh_TW
dc.contributor.author-dept森林環境暨資源學研究所zh_TW
顯示於系所單位:森林環境暨資源學系

文件中的檔案:
檔案 大小格式 
ntu-95-1.pdf
  未授權公開取用
3.46 MBAdobe PDF
顯示文件簡單紀錄


系統中的文件,除了特別指名其著作權條款之外,均受到著作權保護,並且保留所有的權利。

社群連結
聯絡資訊
10617臺北市大安區羅斯福路四段1號
No.1 Sec.4, Roosevelt Rd., Taipei, Taiwan, R.O.C. 106
Tel: (02)33662353
Email: ntuetds@ntu.edu.tw
意見箱
相關連結
館藏目錄
國內圖書館整合查詢 MetaCat
臺大學術典藏 NTU Scholars
臺大圖書館數位典藏館
本站聲明
© NTU Library All Rights Reserved