UV-B辐射、CO_2激光对秦艽生理、生长和有效成分的影响及其加工储藏方法的评价
详细信息    本馆镜像全文|  推荐本文 |  |   获取CNKI官网全文
摘要
为促进陕西省秦艽的产业化发展,本论文以秦艽为材料,分别研究了1,CO_2激光辐照对秦艽种子萌发和幼苗生长的影响;2,大田条件下,补充适量的UV-B辐射对秦艽生理、生长、品质等方面的影响;3,秦艽生药的产地加工及储藏方法初探。所用CO_2激光的功率密度是3.2 mw.mm~(-2),处理时间从0秒到120秒;补充UV-B辐射的剂量分别为2.18 KJ.m~(-2).d~(-1)和3.36 KJ.m~(-2).d~(-1),处理时间从五月初至倒苗前。秦艽的加工方法包括微波,烘干,蒸透,暴晒,掸透,晾干,并研究了储藏的温度条件。
     结果发现:
     (1)较低剂量(30秒~60秒)的CO_2激光处理可以促进秦艽种子的萌发率和发芽势;提高幼苗叶子的总叶绿素、叶绿素a、叶绿素b含量和可溶性蛋白含量,促进秦艽幼苗生长。
     (2)在生长季节,给二年生的秦艽补充适量UV-B辐射,发现增强UV-B辐射对秦艽的生长影响不大,而对其品质产生正效应。两处理组的株高、干重、根重、总叶绿素、叶绿素a含量比对照组略降低,但没有统计意义上的差异;尤其是随着时间的增长,两处理组的生长更少地受到影响。秦艽的紫外吸收物含量升高,PAL含量和可溶性蛋白质含量均增加应该是UV-B辐射增强下植物的防护性措施,从一定程度上保证了植株的生长,并促进了龙胆苦甙含量的增长;可溶性糖含量的降低则可能与UV-B辐射增强下资源分配较多流向次生代谢有关。总之,可以通过补充UV-B辐射的方法来促进秦艽的龙胆苦甙含量,但要注意剂量。
     (3)对秦艽的加工和储藏方法的研究表明:微波法和高温烘干法是较好的产后加工法,可以极大地减少龙胆苦甙的损失。药材干燥后进行遮光冷藏是储存的好方法。考虑到产区实际情况和经济易行性,药农可将鲜样高温烘干,然后放在通风干凉的地方保存,尤其在气候较冷的秋冬季是很好的选择。
To improve the industrialization of Gentiana macrophylla Pall, in shaanxi province, we studied separately: 1, Effects of CO2 laser irradiation on seed germination and seedling growth of Gentiana macrophylla Pall.; 2, Impacts of appropriate supplement of UV-B radiation on physiology, growth and quality of Gentiana macrophylla Pall, under field condition; 3, the methods of processing and store of Gentiana macrophylla Pall.
    The dose of CO2 laser was 3.2 mw.mm-2, the treat time was from Os to 120s; UV-B supplementary dose was 2.18 kJ.m-2.d-1 and 3.36 kJ.m-2.d-1 respectively from 9:00 to 17:00 everyday during growing season (from May to Oct); The processing methods included microwave-drying, drying, braising , insolation , steaming and airing, the temperature condition stored had also been studied.
    The results showed that: (1) CO2 laser irradiation of lower dose (30s - 60s) promoted seed germination, Improved content of total chlorophyll , chlorophyll a , chlorophyll b and soluble protein, and then promoted the seedling growth of Gentiana macrophylla Pall..
    (2) Supplementary UV-B radiation had a little effects on growth but positive effects on quality of biennial Gentiana macrophylla Pall. The height, root weight, total biomass, content of total chlorophyll and chlorophyll a were decreased when compared to ambient controls in growing season, but not obviously different; The growth of two treatment groups were influenced less especially with the continuance of UV-B radiation. In addition, the content of UV absorbing compounds and soluble proteinand PAL enzyme activity of the both treatments were increased as compared with controls. Those positive effects which should be defendent measures of plant to the supplementary radiation, had guaranteed the growth of Gentiana macrophylla Pall in a certain degree and had increased content of gentiopicroside. The reason of reduction of soluble sugar content may be that resource allocated more to secondary metabolism under supplementary UV-B radiation. In a word, we can promote the content of gentiopicroside in Gentiana macr
    ophylla Pall, by supplementing proper
    
    
    
    UV-B radiation.
    (3) The study on the processing and storage showed that microwave drying and high temperature drying were the better processing methods which can reduce gentiopicroside's loss greatly. It is a good method to store Gentiana macrophylla Pall by refrigeration after drying. Allowing for the actual conditions, the planters had better store dried Gentiana macrophylla Pall in cool and ventilated place, that is a good choice especially in autumn and winter.
引文
1.蔡素雯,苑春慧,崔小慧,王永喻.He-Ne激光对玉米幼苗POD和CAT酶活性的影响.应用激光,1993,13(4):181-183
    2.曹恩华.激光对DNA的作用.激光生物学,1993,2:290-295
    3.陈大华,叶和春,李国风,刘彦.植物类异戊二烯代谢途径的分子生物学研究进展.植物学报,2000,42(6):551-558
    4.陈千良.陕西产秦艽的化学成分研究.西北大学硕士学位论文.2003.西安
    5.冯文新,张素梅.He-Ne激光对菘蓝幼苗SOD、CAT活性的影响.山西农业大学学报,1997,17(1):21-23
    6.冯国宁,安黎哲,冯虎元,王勋陵.增强UV-B辐射对菜豆蛋白质代谢的影响.植物学报,1999,41(8):833-836
    7.傅丰永,孙南君.秦艽化学成分的研究(Ⅰ).药学学报,1958,6(4):198
    8.宫川辰治等.龙胆科生药中两种苦甙的含量测定.药物分析杂志,1997,17(4):241
    9.古谷雅村,宫地重远,玖村敦彦主编,崔继林译.植物生理学讲座第二卷:代谢生理.北京,科学出版社,1978:210
    10.龚海洋,王红,许哲.二十一种中药对小鼠免疫药理作用的初步研究.中药药理与临床,1995,11(2):30
    11.郜尽.龙胆苦苷的制备及药代动力学研究.西北大学硕士学位论文.2002.
    12.郭亚健,陆蕴如.龙胆苦苷转化为秦艽丙素等生物碱的研究.药物分析杂志,1983,3(5):268.
    13.何水林,林文雄,陈如凯,白镜焕,申东贤,金吉雄.辣椒倍半萜植保素代谢的分子生态学研究Ⅰ:紫外线对辣椒叶片倍半萜环化酶及鲨烯合成酶的作用.农业生物技术学报,1999,7(4):377-381
    14.侯扶江,贲桂英,颜景义等.田间增加紫外线辐射对大豆幼苗生长和光合作用的影响.植物生态学报,1998,22(3):256-261
    15.胡能书,吴秀山.激光辐照油菜的生物学特性及其同工酶分析.应用激光,1985,5(3):119-121
    16.胡能书,王保仁,吴秀山.激光辐照水稻的生理生化基础研究(Ⅰ).应用激光,1981,
    
    1(3):22—24
    17.胡能书,向洋等.激光辐照水稻的生理生化基础研究(Ⅱ).应用激光,1982,2(5):37-40
    18.近藤嘉和等.秦艽成分研究.生药学杂志,1996,46(3):342-343
    19.籍秀娟,刘耕陶,宋振玉.秦艽生物碱甲的药理作用Ⅱ.生理学报,1959,23(20):151
    20.李元,王勋陵.紫外辐射增加对春小麦生理、产量和品质的影响.环境科学学报,1998,18(5):504-509
    21.李方民.UV-B辐射增强和CO_2施肥的复合作用对冬季大棚番茄品质和产量的影响.西北大学硕士学位论文.2003.西安
    22.李雨润,郝丽珍.CO_2激光辐照提高蔬菜种子活力的研究.激光生物学报,2000,9(2):110-113
    23.李惠娟,王耀芝.秦艽的胚胎学研究.西北植物学报,1994,14(4):243-248
    24.李琳,焦新之.应用蛋白染色剂考马斯亮兰G-250测定蛋白质的方法.植物生理学通讯,1980(6):52-55.
    25.李广粹等.中国医学科学1956年论文报告会论文摘要第二卷:70956
    26.李玉滨等.He-Ne激光处理番茄种子最适剂量的研究.中国激光,1990,17(3):189-192
    27.林植芳,林桂珠,彭长连.亚热带植物叶片紫外-B吸收物质的积累.生态学报,1998,18(1):90-95
    28.刘艳红等.秦艽中的环烯醚萜甙类成分.云南植物研究,1995,15(1):85
    29.梁宏,陆仲康,张雪琴等.氮分子激光对雄性小家鼠生殖细胞染色体畸变率的影响.遗传,1980,2(2):27-28
    30.欧阳光察.植物生理学试验手册,上海植物生理学会主编,上海,上海科学技术出版社,1985:191-192
    31.欧琳,陈荣,陈艳娇等.不同波长激光辐照花生种子的生物学效应.激光生物学报,1998,7(3):198-202
    32.彭绍民.He-Ne激光辐照对大豆生物学效应的研究.应用激光,1985,5(4):165-166
    33.彭绍民.激光辐照水稻育种的研究.应用激光,1984,4(4):179-181
    34.齐智.He-Ne激光处理玉米幼苗可溶性蛋白合成的影响.西北大学硕士学位论文.1998
    
    
    35.权宜淑.中药秦艽的本草学研究.西北药学杂志,1997,12(3):113
    36.孙文基等.秦艽中龙胆苦甙的RP-HPLC法含量测定.药物分析杂志,1994,14(1):41
    37.唐旭东,安黎哲,王勋陵.增强UV-B辐射对蚕豆叶片微粒体膜的一些性质的影响.植物生理学报,1998,24(2):171-176
    38.唐玄之,封国林,邵耀春.激光及激光生物学发展概况.激光生物学报,1999,8(2):157-160
    39.王嶽等.70种药用植物抗菌效能的试验.植物学报,1954,3(2):203
    40.王英,楼之岑.中药秦艽的研究概况.药学通报,1987,22(3):153
    41.王英利,王勋陵,岳明.UV-B及红光对大棚番茄品质的影响.西北植物学报,2000,20(4):590-595
    42.王小箐,潘瑞炽.UV-B对高等植物生长和产量及某些生理代谢过程的影响.植物生理学通讯,1995,31:385-389
    43.吴春清,范艳杰.秦艽鳖甲汤治疗肺痨骨蒸潮热24例.中医药信息,1983,19(3):30
    44.武秀荣等.He-Ne激光对甘兰种子萌发的生物效应.激光生物学,1994,3(4)
    45.肖培根主编.新编中药志第一卷.北京,化学工业出版社,2002:756
    46.向洋.激光生物学.长沙,湖南科学技术出版社,1995:73-226
    47.许梅芬.激光对小麦的诱变效果及其在育种上的应用.浙江农业大学学报,1991,17(1):55-59
    48.许梅芬.激光对小麦的生物学效应的研究.应用激光,1995,15(3):131-134
    49.晏斌,戴秋杰.紫外线辐射对水稻叶组织中活性氧代谢及膜系统的影响.植物生理学报,1996,22(4):375-378
    50.姚宽路,王存劳.秦艽栽培技术研究.基层中药杂志,2001,16(4):47-48
    51.严国忠.激光对大豆生物效应的研究.中国激光,1984,11(11):693-697
    52.袁成业,杨晓冬.秦艽木瓜酒治疗肩周炎73例疗效观察.江苏中医,1990,(9):23
    53.岳明.增强的紫外辐射对竞争性平衡及植物群落的影响.兰州大学博士学位论文.1998.兰州
    54.岳明,王勋陵.紫外线辐射对小麦和燕麦竞争性平衡的影响—小麦和燕麦生物量结构与冠层结构.环境科学学报,1999,19(5):526—531
    55.朱九明.激光辐射在细胞学遗传学领域的应用.激光杂志,1988,9(1):8-12
    
    
    56.张勇.龙胆苦苷药理研究进展.云南医药,1991,12(5):304
    57.张振清.植物生理学实验手册.上海,科技出版社,1985:134
    58.郑有飞,杨志敏,颜景义.作物对太阳紫外辐射增加的生物效应及评估.应用生态学报,1996,7(1):107-109
    59.陕西森林研究学会.林木采种育苗手册,陕西,陕西科技出版社 1984:29
    60.辽宁中草药新医疗法资料选编.1970:41-46
    61.《中华本草》编委会,中华本草第六卷,上海,上海科学技术出版社,1999:231
    62.中科院西北植物研究所编,秦岭植物志,第一卷第四册.北京,科学出版社,1983:112
    63.国家医药管理局中医药情报中心编.植物药有效成分手册.北京,人民卫生出版社,1986:498
    64.A.N.杜布罗夫.紫外线辐射对植物的作用.北京,科学出版社1964:1-21
    65. Akira Nara, Yuichi Takeuchi. Ethylene evolution from tobacco leaves irradiated with UV-B. J Plant Res, 2002, 115: 247-253
    66. Allen D J, Nogue's S, Baker N R. Ozone depletion and increased UV-B radiation: is there a real threat to photosynthesis. J Exp Bot., 1998, 49: 1775-1788
    67. Ambasht N K and Agrawal M. Physiological responses of field grown Zea may. L. plant to enhanced UV-B radiation. Biotronics, 1995, 24(2): 15-23
    68. Back K, He S, Kim K U, Shin D H. Cloning and bacterial expression of sesquiterpene cyclase, a key branch point enzyme for the synthesis of sesquiterpenoid phytoalexin capsidiol in UV-challenged leaves of Capsicum annuaun. Plant Cell Physiol. 1998, 39: 899-904
    69. Back K, Chappell J. Cloning and bacterial expression of a sesquiterpene cyclase from Hyoscyamus muticus and its molecular comparison to related terpene cyclases. J Biol Chem, 1995, 270: 7375-7281
    70. Bacci L, Grifoni D, Sabatini F, Zipoli G. UV-B radiation causes early ripening and reduction in size of fruits in two lines of tomato(Lycopersicon esculentum Mill.). Global Change Biology, 1999, 5(6): 635-646
    71. Bassman J H, Edwards G E, Robberecht R. Long-term exposure to enhanced UV-B radiation is not detrimental to growth and photosynthesis in Douglas-fir. New
    
    Phytologist, 2002,154(1): 107-120
    72. Basiouny F M, Van T K and Biggs R H. Some morphological and biochemical characteristics of C_3 and C_4 plants irradiated with UV-B. Physiol. Plant, 1978,42:29-32
    73. Barnes P W, Flint S D, Caldwell M M. Morphological responses of crop and weed species of different growth form to UV-B radiation. Am. J. Bot., 1990, 77(10): 1354-1361
    74. Beggs C J, Andrea S J, Eckard W. Isoflavonoid formation as an indication of UV stress in bean (phaseolus vulgaris) leaves. Plant Physiol., 1985, 79: 630-634
    75. Beggs C J, Kronenberg G H. Photocontrol of Flavonoid Biosynthesis. Kendrict R E eds. Photomorphogenesis in Plant. Kluwer Academic Dordredt. 1994, 2: 733-750
    76. Beyschlag W, Barnes P W, Flint S D and Caldwell M M. Enhanced UV-B Irradiation Has No Effect on Photosynthetic Characteristics of Wheat (Triiicum aestivum L.) and Wild Oat (Avenafatua L.)under Greenhouse and Field Conditions. Photosynthetica, 1988, 22(5)
    77. Biggs R H and Kouthus SV. UV-B biological and climate effects research. Final Report(1978). Department of Agriculture/Environmental Protection Agency. Washington, DC. US.
    78. Bjorn L O. Effects of Ozone depletion and increased UV-B on terrestrial ecosystems. Intern. J. Environmental Studies, 1996,51:217-243
    79. Bjorn L O, Callaghan T V, Johnsen I et al. The effects of UV-B radiation on European heathland species. Plant Ecology, 1997, 128:252-264
    80. Bouvier F, D' Harlingue A, Suire C, Backhaus R A, Camara B. Dedicated roles of plastid transketolases during the early onset of isoprenoid biogenesis in pepper fruits. Plant Physiol, 1998, 117: 1423-1431
    81. Bors W, Heller W, Michel C K. Electron paramagnetic resonance studies of flavonoid compounds. In: G. Poli, E. Albano ed. Free radicals: From basic science to medicion, Basel: Birkharse. 1993: 528
    82. Brandt K, Giannini A, Lercari B. Photomorphogenic responses to UV radiation Ⅲ A comparative study of UV-B effects on anthocyanin and flavonoid accumulation
    
    in wild-type and aurea mutant of tomato (Lycopersicon esculentum Mill.). Photochem. Photobiol., 1995, 62: 1081-1087
    83. Braun J, Tevini M. Regulation of UV-protective pigment synthesis in the epidermal layer of rye seedlings (secale cereale L. cv. Kustro). Photochem. Photobiol., 1993, 57: 318-323
    84. Brandle J R, Campbell W F, Sisson W B et al. Net photosynthesis, electron transport capacity and ultrastructure of pisum sativuml exposed to ultraviolet-B radiation. Plant Physiol., 1977, 60: 165-168
    85. Bryant J P, Chapin F S, Klein D R. Carbon/nutrient balance of boreal plants in relation to vertebrate herbivory. Oikos., 1983, 40: 357-368
    86. Burchard P, Bilger W, Weissenbock G. Contribution of hydroxycinnamates and flavonoids to epidermal shielding of UV-A and UV-B radiation in developing rye primary leaves as assessed by ultraviolet-induced chlorophyll fluorescence measurements. Plant Cell and Environment, 2000, 23(12): 1373-1380
    87. Cai S W, Zhao X.S, Lu FT, Jiang J Q. The influence of He-Ne laser irradiation on the active oxygen metabolism of corn seedling. Chinese J of Laser, 1994, 9: 767-769
    88. Cabor G L, Mikos G. The role of the genome projection determining gene function insights from model organisms. Cell, 1996, 86: 521-529
    89. Caldwell M M. Solar UV radiation and the growth and development of higher plant. Photophysiology(A.C. Giese, ed.), 1971,6:131-177, Academic Press, New York
    90. Caldwell M M, Robberecht R and Flint S D. Internal filters: Prospects for UV-acclimation in higher plants. Physiol. Plant, 1983, 58: 445-450
    91. Caldwell M M, Flint S D. Stratospheric ozone reduction, solar UV-B radiation and terrestrial ecosystem. Clim. Change, 1994,27:375-394
    92. Caldwell M M, Teramura A H. Effects of increased solar ultraviolet radiation on terrestrial plants. Ambio, 1995,24 (3): 165-172
    93. Casal J J, Sanchez R A and Deregibus V A. Tillering responses of Lolium multiflorum plants to changes of red/far red ratio typical of sparse canopies. J. Exp. Bot., 1987, 38: 1432-1439
    
    
    94. Cen Y P, Bomman JF. The effect of exposure to enhanced ultraviolet -B radiation on the penetration of monochromatic and polychromatic ultraviolet -B radiation in leaves of Brassica napus. Physiol. Plant, 1993,87:247
    95. Chang D C N, Campbell W F. Response of Tradescantia stamen hairs and pollen to UV-B irradiation. Environ. Exp. Bot., 1976,16: 195-199
    96. Chapin F S, Bloom A J, Field C B and Warning R H. Plant responses to multiple environmental factors. Bioscience, 1987, 37: 49-57
    97. Charles Burke and Rodney Croteau. Interaction with the small subunit of Geranyl diphosphate synthase modifies the chain length specificity of geranylgeranyl diphosphate synthase to produce geranyl diphosphate. The Journal of Biological Chemistry, 2002,277(5): 3141-3149
    98. Chappell J. The biochemistry and molecular biology of isoprenoid metabolism. Plant Physiol., 1995, 107: 1-6
    99. Chen X-Y, Chen Y, Heinstein P, Davisson V J. Cloning, expression, and characterization of (+)-δ-cadinene synthase: A catalyst for cotton phytoalexin biosynthesis. Arch BiochemBiophysics, 1995, 324: 255-266
    100. Choi D, Ward B L, Bostock R M. Differential induction and suppression of potato 3-hydroxy-3-methylglutaryl coenzyme A reductase genes in response to Phytophthora infestans and to its elicitor arechidonic acid. Plant Cell, 1992, 4: 1333-1344
    101. Coley P D. Costs and benefits of defensive by tannins in a neotropial tree. Oecologia, 1986,70:238-241
    102. Colby S M, Crock J, Dowdle-Rizzo B, Lemaux P G, Croteau R. Germacrene C synthase from Lycopersicon esculentum cv. VFNT Cherry tomato: cDNA isolation, characterization, and bacterial expression of the multiple product sesquiterpene cyclase. Proc Natl Acad Sci USA, 1998, 95: 2216-2221
    103. Dai Q J, Peng Shaobing and coronel V P. Intraspecific responses of 188 rice cultivars to enhanced UV-B radiation. Environ. Exp. Bot. , 1994, 34: 433-442
    104. Day T A, Demchik S M. Influence of enhanced UV-B radiation on biomass allocation and pigment concentrations in leaves and reproductive structures of greenhouse-grown Brassica rapa. VEGETATIO, 1996a, 127 (2): 109-116
    
    
    105. Day T A, Howells B W, Ruhland C T. Changes in growth and pigment concentrations with leaf age in pea under modulated UV-B radiation field treatments. Plant Cell And EnvironmenC 1996b 19 (1): 101-108
    106. Day T A. Ultraviolet radiation and plant ecosystems. In: Ecosystems, Evolution, and Ultraviolet Radiation. Cockell C S and Blaustein A R(ed.). New York: Springer-Verlag, 2001:80-117.
    107. Doanhue S J, Taylor J S and Reines D. Transcript cleavage by RNA polymerase (2) arrested by a cyclobutane dimer in the DNA template. Proc. Natl. Acad Sci. USA. 1994, 91: 8502-8506
    108. D'Surney S J, Tschaplinski T J, Edwards N T and Shugart L R. Biological responses of two soybean cultivars exposed to enhanced UV-B radiation. Environ. Exp. Bot., 1993, 33: 347-356
    109. Elena Kostina, Anu Wulff, Riitta Julkunen-Tiitto. Growth, structure, stomatal responses and secondary metabolites of birch seedlings (Betula pendula) under elevated UV-B radiation in the field. Trees. 2001, 15: 483-491
    110. Facchini P J, Chappell J. Gene family for an elicitor-induced sesquiterpene cyclase in tobacco. Proc Natl Acad Sci USA, 1992, 89: 11088-11092
    111. Feder W A and Shrier R. Combination of UV-B and ozone reduces pollen tube guowth more than either stress alone. Environ. Exp. Bot., 1990, 30: 451-454
    112. Fischbach R J, Kossmann B, Panten H etal. Seasonal accumulation of ultraviolet-B screening pigments in needles of Norway spruce (Picea abies (L.) Karst). Plant Cell and Environment, 1999, 22(1): 27-37
    113. Fiscus E L, Booker F L. Is increases UV-B a threat to crop photosynthesis and productivity. Photosynthesis Research, 1995,43(2): 81-92
    114. Flint S D, Caldwell M M. Partial inhibition of in vitro pollen germination by simulated solar ultraviolet-B radiation. Ecology, 1984,65(3): 792-795
    115. Giuseppe D C, Bartdomeo L. Use of UV radiation for control of height and condition of tomato transplant. Scientia Horticulture, 1997, 71: 27-34.
    116. Giannini A, Parclossi A and Lercari B. The use of UV radiation to control the architecture of salvia splends plant: Effect on plant growth, water relations and
    
    gas exchange. Photochemistry and photobiology, 1996, 64(1):123-130.
    117. Gordon D C, Percy K E, Riding R T. Effects of UV-B radiation on epicuticular wax production and chemical composition of four Picea species. New Phytologist, 1998, 138(3): 441-449
    118. Grammatikopoulos G, Kyparissis A, Drilias P, Petropoulou Y, Manetas Y. Effects of UV-B radiation on cuticle thickness and nutritional value of leaves in two mediterranean evergreen sclerophylls. Journal of plant physiology, 1998,153 (3-4): 506-512
    119. Green R, Fluhr R. UV-B induced PR-1 Accumulation is mediated by active oxygen species. Plant Cell 1995, 7: 203-212
    120. Gregianini T S, da Silveira V C, Porto D D, Kerber V A, Henriques A T, Fett-Neto A G. The alkaloid brachycerine is induced by ultraviolet radiation and is a singlet oxygen quencher. Photochemistry and photobio]ogy, 2003, 78(5): 470-474
    121. Gwynn-Jones D. Short-term impacts of enhanced UV-B radiation on photoassimilate allocation and metabolism: a possible interpretation for time-dependent inhibition of growth. Plant Ecology, 2001, 154 (1-2)
    122. Hanns Frohnmeyer, Chris Bowler, Jian-Kang Zhu, Hiroshi Yamagata, Eberhard Schafer, Nam-Hai Chua. Different roles for calcium and calmodulin in phytochrome and UV-regulated expression of chalcone synthase. The Plant Journal, 1998, 13(6): 763-772
    123. Hopkins L, Bond M A and Tobin A K. Effects of UV-B on the development and ultrastructure of the primary leaf of wheat(Triticum aestivum). J. Exp. Bot., 1996, 47(9): 20
    124. Hollosy F. Effects of ultraviolet radiation on plant cells. Micron, 2002,33 (2): 179-197
    125. Jenkins G I, Fugrevand G. UV-B protection and signal transduction. In: P. Lumsden ed. Plants and UV-B. Cambridge: Cambridge University Press, 1997: 136-156
    126. Jordan B R etal. Change in mRNA leaves and polypeptide subunits of ribulose-1,5-bisphosphate carboxylase in response to supplementary UV-B radiation. Plant Cell and Environment, 1992, 15(1): 91-98
    
    
    127. Jordan B R et al. The effect of UV-B radiation on gene expression and pigment composition in etiolated and green pea leaf tissue: UV-B induced changes are gene-specific and dependent upon the developmental stage. Plant Cell and Environment, 1994, 17(1): 45-54
    128. Johanson U, Gehrke C, Bjorn L O. The effects of enhanced UV-B radiation on a subarctic heath ecosystem. Ambio, 1995, 24: 106-111
    129. Johnson-Thompson M, aalpern J B and Jackson W M et al. Vacuum UV laser induced scis-sion of simian virus40 DNA. Photochem. Photobiol., 1984, 39(1): 17-24
    130. Junko Takeda, Ichiro Obi, Kazuichi Yoshida. Action spectra of phenylalanine ammonia- lyase and chalcone synthase express in carrot cells in suspension. Physiologia Plantarum 1994, 91: 517-521,
    131. J C Long, G I Jenkins. Involvement of plasma membrane redox activity and calcium homeostasis in the UV-B and UV-A blue light induction of gene expression in Arabidopsis. Plant Cell, 1998, 12: 2077-2086
    132. Klebanov G, Kapitanov A B, Tesslkin Y A. The antioxidant properties of lycopene. Biologicheskie Membrany Moscow, 1998, 15(2): 22—25
    133. K C Smith. Programmer of The First Meeting of the International Laser Therapy Association, 1990(10): 130-141.
    134. Laakso K, nuttunen S. Effects of the ultraviolet-B radiation (UV-B) on conifers: a review. Environmental Pollution, 1998, 99 (3): 319-328
    135. Lavola Anu. Accumulation of flavonoides and related compounds in birth induced by ultraviolet-B radiation. Tree Physiology, 1998, 18: 53-58
    136. Langer B. and Wellman E. Phytochrome induction of photoreactivating enzyme in Phaseolus vulgaris L. seedings. Photochem. Photobil., 1990, 52: 861-863
    137. Lange B M, Wildung M R, McCaskill D, Croteau R. A family of transketolases that directs isoprenoid biosynthesis via a mevalonate-independent pathway. Proc Natl Acad Sci USA, 1998, 95: 2100-2104
    138. Li J Y, Qulee T M, Raba R. Arabidopsis flavonoid mutants are hypersensitive to UV-B radiation. The Plant Cell, 1993,5:171-179
    139. Lois R, Buchanan B B. Severe sensitivity to UV radiation in an arabidopsis
    
    mutant deficient in a flavonoid accumulation. Planta, 1994,194: 504-509
    140. Masaharu N. Cytogenetic effects of argon laser irradiation on chinese hamster cells, Radiat. Res., 1983, 93(3): 598-608
    141. Mau C J D, West C A. Cloning of casbene synuhase CDNA: Evidence for conserved structural features among terpenoid cyclases in plants. Proc Natl Acad Sci USA, 1994, 91: 8497-8501
    142. Mckenzie R L, Bjrn L O, Bais A, llyas M. Changes in biologically active ultraviolet radiation reaching the Earth's surface. Photochemical and Photobiological Sciences, 2003, 2: 5-15
    143. M. Ito Al, Y. Ichinose Al, H. Kato Al, T. Shiraishi A L, T. Yamada Al. Molecular evolution and functional relevance of the chalcone synthase genes of pea. Mol. Gen. Genet. 1997, 255: 28-37
    144. Murali N S, Teramura A H. Effects of ultraviolet -B irradiance on soybean. Ⅵ. Influence of phosphorus nutrition on growth and flavonoid content. Physiol. Plant. 1985, 63: 413-416
    145. Murali N S, Teramura A H. Intraspecific differences in Cucumis sativu sensitivity to UV-B radiation. Physiol. Plant, 1986, 68: 673-677
    146. Mark U, Saile-Mark M and Tevini M. Effects of solar UV-B radiation on growth, flowering and yield of central and southern European maize cultivars (Zea mays L.). Photochem. Photobiol., 1996, 64(3): 457-463
    147. Murphy T M. Membranes as targets of ultraviolet radiation. Physiol. Plantarum, 1983, 58: 381-388
    148. Mirecki R M, Teramura A H. Effects of ultraviolet-B irradiance on soybean. V. The dependence of plant sensitivity on the photosynthetic photon flux density during and after leaf expansion. Plant physiol., 1984,74:475-480
    149. Musil C F. Differential effects of elevated UV-B radiation on the photochemical and reproductive performances of dicotyledonous and monocotyledonous arid-environment ephemeris. Plant Cell Environ., 1995, 18: 844-854
    150. M. P. Puglisi, Y. J. Paul. Intraspecific variation in the red alga Portieria
    
    hornemannii: monoterpene concentrations are not influenced by nitrogen or phosphorus enrichment. Marine Biology, 1997,128:161-170
    151. Norton L R, McLeod A R, Greenslade P D, Firbank L G, Watkinson A R. Elevated UV-B radiation effects on experimental grassland communities. Global Change Biology, 1999,5(5): 601-608
    152. Nedunchezhian N and Kwlandaivelu G. Effect of UV-B radiation on ribulose-1, 5-carboxylase in leaves of vigra sinensis L. Photosynthetica, 1992, 25(3): 431-435.
    153. Olson L E W, Schimmerling and Tobias C, Laser action spectrum of reduced excitability in nerve cells. Brain Res, 1981, 204, (2): 436-440
    154. Paleg L G, Aspinall D. Field control plant growth and development through the laser activation of phytochrome. Nature, 1970: 970-973.
    155. Pang Q and Hays J B. UV-B inducible and temperature-sensitive photoreactication of cylobutane and pyrimidine dimers in Arabidopsis thaliana. Plant Physiol., 1991,95:536-543
    156. P B F Ouwerkerk, T O Trimborn, F Hilliou, J Memelink. Nuclear factors GT-1 and 3AF1 interact with multiple sequences within the promoter of the TDCgene from Madagascar. periwinkle: GT-1 is involved in UV light-induced expression. Mol. Gen. Genet., 1999, 261: 610±622
    157. Quaite F E, Sutherland B M and Sutherland J C. Action spectrum for DNA damage in alfalfa lowers predicted impact of ozone depletion. Nature, 1992, 358: 576-578
    158. Quaite F E, Sutherland B M, Sutherland J C. Quantitation of pyrimidine dimers in DNA from UV-B-irradiated alfalfa(Medicago sativa L.)seedlings. Appl. Theoret. Electrophor.,1993, 2: 171-175
    159. Robberecht R, Caldwell M M and Billions D W. Leaf Ultraviolet optical properties along a latitudinal gradient in the arctic-alpine life zone. Ecology, 1980, 61: 612-619
    160. Robberecht R, Caldwell M M. Protective mechanisms and acclimation to solar ultraviolet-B radiation in oenotherza strieta. Plant cell Environ., 1983, 6: 477-485
    161. Robberecht R, Caldwell M M. Leaf UV optical properties of Rumex patientia L.
    
    and Rumex Obtusifolius L. in regard to a protective mechanism against solar UV-B radiation injury. In R C Worrest and Caldwell M M(ed.) Stratospheric ozone reduction, solar ultraviolet radiation and plant life. Springer-Verlag, Berlin, 1986:250-259
    162. Rozema J, Lenssen G M, Van de staaij W Met al. Effects of UV-B radiation on terrestrial plants and ecosystems: Interaction with CO_2 enrichment. Plant Ecol., 1997,128:182-191
    163. Rozema J, Teramura A, Caldwell M. Atmospheric CO_2 enrichment and enhanced solar ultraviolet-B radiation: gene to ecosystem processes. In: Luo Y, Mooney H. A. ed. Carbon dioxideand environmental stress. New York, Academic Press, 1999: 169-191
    164. Robak J, Shridi F, Wolbis Metal. Screening of the influence of flavonoids on lipoxygenase and cyclooxygenase activity, as well as nonenzymic lipid oxidation. Pol. J. Pharmacol. Pharm., 1990, 40: 793-797
    165. Rosa T M, Julkunen-Tiitto R, Lehto T etal. Secondary metabolites and nutrient concentrations on silver birch seedlings under five levels of daily UV-B exposure and two relative nutrient addition rates. New Phytologist, 2001,150:121-131
    166. Ros J, Tevini M. Interaction of UV-B radiation and IAA during growth of seedling and hypocitul segments of sunflower, J. Plant Physiol., 1995, 146: 295-302
    167. Santon I, Almeida J M, Salema R. Plants of Zea mays L. Developed under enhanced UV-B radiation Ⅰ Some ultrastructural and biochemical aspects, J. Plant Physiol. 1993, 141: 450-456
    168. Senger H, Schmidt W. Diversity of photoreceptors. In: R.E. Kendrick and G.H.M. Kronenberg ed. Photomorphogenesis in Plants. Dordrecht, The Netherlands: Martinus Nijhoff/Dr. W. Junk Publishers, 1986: 137-158
    169. Searles P S, Caldwell M M and Winter K, The response of five tropical dicotyledon species to solar ultraviolet-B radiation. American Journal of Botany, 1995, 82(4): 445-453
    170. Searles P S, Flint S D, Caldwell M M. A meta-analysis of plant field studies simulating stratospheric ozone depletion. Oecologia, 2001, 127: 1-10
    171. Smith K C. Programme of The First Meeting of the International Laser Therapy Association. 1990(10): 130-141
    
    
    172. Sreuber J F, Bornman G etal. A flavonoid mutant of barley(hordeum vulgare L.) exhibits increased sensitivity to UV-B radiation in the primary leaf. Plant Cell and Environment, 1996, 19: 593-601
    173. Stapleton A E, Walbot V. Flavonoids can protect maize DNA from the inducing of UV radiation damage. Plant Physiology, 1994, 105: 881-889
    174. Staxen L and Bornman J F. A morphological and cytological study of petunia hybrida exposed to UV-B radiation. Physiologia Plantarum, 1994, 91: 735-740
    175. Sullivan J H and Teramura A H. The effects of UV-B radiation on loblolly pine Ⅰ Growth, photosynthesis and pigment production in greenhouse-grown seedlings. Physiologia Plantarum, 1989, 77: 202-207
    176. Sullivan J H and Teramura A H. Field study of the interaction between solar ultraviolet-B radiationand drought on photosynthesis and growth in soybean. Plant Physiol., 1990,92:141-146
    177. Sullivan J H, Teramura A H. The effects of UV-B radiation on loblolly pine 3. Interaction with CO_2 enhancement. Plant Cell and Environ.,1994,17:311-317
    178. Tan R Xetal. Acylsecoiridiods antifungal constituents from Gentiana macrophylla. Phytochemistry, 1997, 43(5): 1205
    179. Tegelberg R, Tegelberg R J-T, Pedroj A. The effect of long term elevated UV-B radiation on the growth and phenolics of field-grown silver birch (Betula pendula). Global change Biology, 2001, 7: 839-848
    180. Tevini M, Iwanzik W, Thoma U. Some effects of enhanced UV-B irradiation on the growth and composition of plants. Planta, 1981, 153: 388-394
    181. Tevini M, Teramura A H. UV-B effects on terrestrial plants. Photochemistry and Photobiology, 1989, 50: 479-483.
    182. Tevini M, Braun J, Fieser G. The protective function of the epidermal layer of rye seedling against ultraviolet-B radiation. Photochem. Photobiol., 1991, 53: 329-333
    183. Teramura A H, Biggs R H, Kossuth S. Effects of UV-B radiation on soybean Ⅱ. Plant Physiol., 1980, 65: 483-487
    184. Teramura A H, Tevini M. Effects of ultraviolet-B radiation on the growth and
    
    yield of crop plants. Physiol. Plant, 1983, 58: 415-427
    185. Teramura A H, Sullivan J H, Lydon J. Effects of UV-B radiation on soybean yield and seed quality: A six-year field study. Physiol. Plant, 1990, 80: 5-11
    186. Teramura A H, Ziska L H, Sztein A E. Changes in growth and photosynthetic capacity of rice with increased UV-B radiation. Physiol. Plant, 1991, 83: 373-380
    187. Taylor R M, Tobin A K and Bray C M. The effects of enhanced UV-B irradiation on DNA damage and repair in plant tissue. J. Exp. Bot., 1994, 45: 55-61
    188. Taylor R M. etal Ultraviolet-B induced DNA lesions and their removal in wheat(Triticum aestivum L.). Plant Cell Environ., 1996, 19(2): 171-181
    189. Veteli T O, Tegelberg R, Pusenius J, Sipura M, Julkunen-Tiitto R, Aphalo P J, Tahvanainen J. Interactions between willows and insect herbivores under enhanced ultraviolet-B radiation. Oecologia, 2003, 137(2): 312-320
    190. Vu C V, Allen L H, Garrard L A. Effects of supplemental UV-B radiation on primary photosynthetic carboxylating enzymes and soluble proteins in leaves of C_3 and C, crop plants. Physiol. Plant, 1982, 55: 11-17
    191. Warren J M, Bassman J H, Eigenbrode S. Leaf chemical changes induced in Populus trichocarpa by enhanced UV-B radiation and concomitant effects on herbivory by Chrysomela scripta (Coleoptera: Chrysomelidae). Tree Physiology, 2002,22 (15-16): 1137-1146
    192. Werner Edgar, Gla gen, Anette Rose, Johannes Madlung, Wolfgang Koch, Johannes Gleitz*, Hanns Ulrich Seitz. Regulation of enzymes involved in anthocyanin biosynthesis in carrot cell cultures in response to treatment with ultraviolet light and fungal elicitors. Planta, 1998, 20: 490±498
    193. Wildung M R, Croteau R. A cDNA clone for taxadiene synthase, the diterpene cyclase that catalyzes the committed step of taxol biosynthesis. J Boiol Chem., 1996, 271: 9201-9204
    194.Witham F H,Blaydes D F,Devlin R M.植物生理学实验.北京,科学出版社,1974:73—76.
    195. Willekens H, Camp W V, Montagu M V, Inze D, Langebartels C, Sandermann H Jr. Ozone, sulferdioxide and ultraviolet B have similar effect on mRNA accumulation of
    
    antioxidant genes in Nicotiana plumbaginifolia(L.). Plant Physiol, 1994, 106: 1007-1014
    196. Woodall G S, Steward G R. Do anthocynins play a role in UV protection of the red juvenile leaves of Syzygium? Exp. Bot., 1998, 49: 1447-1450
    197. Zavala J A, Ravetta D A. The effect of solar UV-B radiation on terpenes and biomass production in Grindelia chiloensis (Asteraceae), a woody perennial of Patagonia, Argentina. Plant Ecology, 2002, 161(2): 185-191
    198. Zepp, R G, Callaghan TV and Erickson DJ. Effects of increased solar ultraviolet radiation on biogeochemical cycles. Ambio, 1995,24:181-187
    199. Ziska L H, Teramura A H and Sullivan J H. Physiolgical senstivity of plants along an elevational gradient to UV-B radiation. Am. J. Bot., 1992, 79: 863-871

© 2004-2018 中国地质图书馆版权所有 京ICP备05064691号 京公网安备11010802017129号

地址:北京市海淀区学院路29号 邮编:100083

电话:办公室:(+86 10)66554848;文献借阅、咨询服务、科技查新:66554700