荒漠藻类对紫外辐射的响应及其结皮形成的研究
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摘要
以爪哇伪枝藻(Scytonema javanicum (Kütz.) Born et Flah)、具鞘微鞘藻(Microcoleus vaginatus Gom.)和纤细席藻(Phormidium tenue (Menegh.) Gom.)为材料,研究了前两种荒漠藻在紫外线(UV)辐射下的形态和超微结构、生理生化特性的变化以及它们消除因UV辐射所导致的氧化胁迫的机理;还对三种荒漠藻规模化培养条件进行了优化,并对它们藻结皮的培植与发育、藻结皮发育阶段理化性质的改变等进行了细致地研究。
经UV辐射后,S. javanicum细胞的直径和体积变小。在增强的UV-B辐射下,培养物变黄且生物量下降,藻细胞沉于液体培养基底部;而在UV-A辐射下,培养物浓度增加,藻细胞浮于液面。通过电镜发现,经UV辐射后,藻细胞中脂肪颗粒和多糖颗粒等与对照相比都有所增加;经UV-A处理后,藻细胞内片层结构更明显,几乎充满整个细胞;在UV-B处理后的藻细胞横切面周边区有一圈透亮小点。
对S. javanicum和M. vaginatus的光合作用研究发现,在低剂量(低于0.4 mW cm-2)的UV-A处理下,S. javanicum的Fv/Fm比值开始出现下降,但随后又上升,48 h后超过对照组,总体上呈现轻微上升。而UV-A使M. vaginatus的Fv/Fm比值有很小的下降。这些说明UV-A辐射对荒漠藻的光合作用影响不大。0.48 mW cm-2的UV-B辐射处理72 h后,S. javanicum的Fv/Fm比值下降到很低水平。UV-B辐射剂量小于0.06 mW cm-2时,S. javanicum的光合放氧速率随剂量的增加而降低较缓慢;当剂量超过0.06 mW cm-2后,光合放氧速率快速降低,当剂量达到0.48 mW cm-2时,藻体的净光合速率为负值。说明较高剂量的UV-B辐射可显著抑制光合作用。
UV辐射对S. javanicum和M. vaginatus的色素变化具有重要影响。UV-A促进这两种荒漠藻叶绿素a、scytonemin、类胡萝卜素和藻蓝蛋白等色素的合成。在UV-B辐射下,S. javanicum和M. vaginatus的叶绿素和藻蓝蛋白含量快速下降,0.48 mW cm-2剂量的UV-B处理96 h后,这两种色素含量已经下降到很低水平。UV-B促进保护色素伪枝藻素和其它类胡萝卜素的合成,辐射剂量越高作用越明显。
UV辐射对藻细胞中可溶性蛋白质、胞内总糖和胞外多糖(EPS)的积累具
Scytonema javanicum (Kütz.) Born et Flah, Microcoleus vaginatus Gom. and Phormidium tenue (Menegh.) Gom., isolated from desert microbial crusts by Dr. C.X. HU, were used as experimental materials. Effects of UV radiation on the morphology and ultrastructure of S. javanicum, and on the physiological and biochemical characteristics of S. javanicum and M. vaginatus were studied. Those that the mechanism of oxidative stress by UV-B radiation, the optimized cultivation conditions for mass culture, the implantation and development of man-made algal crust in field and physical-chemical properties of artificial algal crust were also studied. The main results were shown as the followings:
After exposure to an enhanced UV-B radiation, both morphology and ultrastructure of S. javanicum changed, the diameter and volume of cells diminished, biomass decreased and population color got yellowing in the culture. The laminar structure became more visible, and increasing number of polysaccharides and fat granules were displayed.
Under UV-A radiation, changes in Fv/Fm of S. javanicum had such a trend: firstly decreased, then increased even exceeded the controls in 48hrs. To M. vaginatus, the Fv/Fm had a slightly decrease. These changes suggested the photosynthesis of algae was somewhat related with UV-A radiation. Undeer 0.48
经UV辐射后,S. javanicum细胞的直径和体积变小。在增强的UV-B辐射下,培养物变黄且生物量下降,藻细胞沉于液体培养基底部;而在UV-A辐射下,培养物浓度增加,藻细胞浮于液面。通过电镜发现,经UV辐射后,藻细胞中脂肪颗粒和多糖颗粒等与对照相比都有所增加;经UV-A处理后,藻细胞内片层结构更明显,几乎充满整个细胞;在UV-B处理后的藻细胞横切面周边区有一圈透亮小点。
对S. javanicum和M. vaginatus的光合作用研究发现,在低剂量(低于0.4 mW cm-2)的UV-A处理下,S. javanicum的Fv/Fm比值开始出现下降,但随后又上升,48 h后超过对照组,总体上呈现轻微上升。而UV-A使M. vaginatus的Fv/Fm比值有很小的下降。这些说明UV-A辐射对荒漠藻的光合作用影响不大。0.48 mW cm-2的UV-B辐射处理72 h后,S. javanicum的Fv/Fm比值下降到很低水平。UV-B辐射剂量小于0.06 mW cm-2时,S. javanicum的光合放氧速率随剂量的增加而降低较缓慢;当剂量超过0.06 mW cm-2后,光合放氧速率快速降低,当剂量达到0.48 mW cm-2时,藻体的净光合速率为负值。说明较高剂量的UV-B辐射可显著抑制光合作用。
UV辐射对S. javanicum和M. vaginatus的色素变化具有重要影响。UV-A促进这两种荒漠藻叶绿素a、scytonemin、类胡萝卜素和藻蓝蛋白等色素的合成。在UV-B辐射下,S. javanicum和M. vaginatus的叶绿素和藻蓝蛋白含量快速下降,0.48 mW cm-2剂量的UV-B处理96 h后,这两种色素含量已经下降到很低水平。UV-B促进保护色素伪枝藻素和其它类胡萝卜素的合成,辐射剂量越高作用越明显。
UV辐射对藻细胞中可溶性蛋白质、胞内总糖和胞外多糖(EPS)的积累具
Scytonema javanicum (Kütz.) Born et Flah, Microcoleus vaginatus Gom. and Phormidium tenue (Menegh.) Gom., isolated from desert microbial crusts by Dr. C.X. HU, were used as experimental materials. Effects of UV radiation on the morphology and ultrastructure of S. javanicum, and on the physiological and biochemical characteristics of S. javanicum and M. vaginatus were studied. Those that the mechanism of oxidative stress by UV-B radiation, the optimized cultivation conditions for mass culture, the implantation and development of man-made algal crust in field and physical-chemical properties of artificial algal crust were also studied. The main results were shown as the followings:
After exposure to an enhanced UV-B radiation, both morphology and ultrastructure of S. javanicum changed, the diameter and volume of cells diminished, biomass decreased and population color got yellowing in the culture. The laminar structure became more visible, and increasing number of polysaccharides and fat granules were displayed.
Under UV-A radiation, changes in Fv/Fm of S. javanicum had such a trend: firstly decreased, then increased even exceeded the controls in 48hrs. To M. vaginatus, the Fv/Fm had a slightly decrease. These changes suggested the photosynthesis of algae was somewhat related with UV-A radiation. Undeer 0.48
引文
安黎哲. 增强的 UV-B 辐射对植物生长、生理代谢及 ACC 合成酶基因表达的影响. 兰州: 兰州大学, 1997.
陈荷生. 沙坡头地区生物结皮的水文物理特点及其环境意义. 干旱区研究, 1992, 9(1): 31-38.
陈坤, 朱涛, 娄元伟, 饶本强. 紫外线(UV)-B 辐射增强对植物影响的研究进展. 信阳师范学院学报, 2004, 17(3): 359-366.
陈兰周, 刘永定, 李敦海. 盐胁迫对爪哇伪枝藻(Scytonema javanicum)生理生化特性的影响. 中国沙漠, 2003, 23(3): 285-288.
陈兰周, 刘永定, 李敦海, 沈银武, 谢作明. 荒漠藻类及其结皮的研究. 中国科学基金, 2003, 17(2):90-93.
陈兰周, 刘永定, 宋立荣. 微鞘藻胞外多糖在沙漠土壤成土中的作用. 水生生物学报, 2002, 26(2): 155-159.
陈善文, 武宝杆. 藻类对 UV-B 增强的响应及其分子基础. 暨南大学学报, 2000, 21(5): 88-94.
陈拓, 任红旭, 王勋陵. UV-B 辐射对小麦抗氧化系统的影响. 环境科学学报, 1999, 19 (4): 453-455.
陈祝春. 沙丘结皮层形成过程的土壤微生物和土壤酶活性. 环境科学, 1991, 12(1): 19-23.
陈祝春. 不同地带沙丘结皮层的土壤酶活性. 中国沙漠, 1989, 9(1): 85-92.
陈祝春, 李定淑. 固沙植物根际微生物对于沙土发育和流沙固定的影响. 生态学杂志, 1987, 6 (2): 6-12.
崔健宇, 江荣风. 土壤农化分析实验. 北京: 中国农业大学出版社, 1998.
崔燕, 吕贻忠, 李保国. 鄂尔多斯沙地土壤生物结皮的理化性质. 土壤, 2004, 36 (2): 197-202.
段争虎, 刘新民, 屈建军. 沙坡头地区土壤结皮形成机理的研究. 干旱区研究, 1996, 13(2): 31-36.
关桂兰, 杨玉锁, 郭沛新. 新疆干旱地区陆生固氮蓝藻的种群、分布及对环境的作用.干旱区研究,1995,12(1): 1-6.
郭宝江, 庞启深, 阮继红. 螺旋藻多糖对植物细胞辐射遗传损伤的防护效应. 植物学报, 1992, 34: 809-812.
黄泽波. 丝状蓝藻水溶性多糖的研究. 中国科学院水生生物研究所博士论文,1997.
黄泽波, 刘永定. 蓝细菌多糖及其应用研究概况. 生物技术通报, 1997, 4: 26-32.
胡春香. 荒漠藻类及其结皮机理研究. 中国科学院水生生物研究所博士论文, 1999.
胡春香, 刘永定, 宋立荣, 黄泽波. 半荒漠藻结皮中藻类的种类组成和分布. 应用生态学报, 2000a, 11(1): 61-65.
胡春香, 刘永定, 黄泽波, 宋立荣. 荒漠藻壳的精细结构与发育. 水生生物学报, 2000b, 24(1): 11-18.
胡春香, 刘永定, 宋立荣. 土壤藻研究新进展. 水生生物学报, 2002a, 26(5): 521-528.
胡春香, 刘永定, 张德禄等. 荒漠藻结皮的胶结机理. 科学通报, 2002b, 47(12): 931-937.
胡春香, 刘永定. 土壤藻生物量及其在荒漠结皮的影响因子. 生态学报, 2002c, 23(2): 284-292.
胡春香等. 宁夏回族自治区沙坡头地区半荒漠土壤中藻类的垂直分布. 生态学报, 2003, 23(1): 38.
姜海波, 邱保胜. 蓝藻对 UV-B 增强的响应与适应. 西北植物学报, 2005, 25(6): 1259-1268.
贾志军, 王小平. 黄土表面结皮对夏闲坡耕地土壤水分的影响研究. 中国水土保持, 2002, 9: 18-20.
康金花, 关桂兰等. 陆生固氮蓝藻对土壤环境的影响. 干旱区研究, 1998, 15(3): 30-33.
李敦海, 刘永定. 近十年中国地木耳研究概况. 水生生物学报, 2003, 27(4): 408-412.
李敦海. 拟球状念珠藻(葛仙米)形态建成与发育及其生理学研究. 中国科学院水生生物研究所博士论文, 2000a.
李敦海, 宋立荣, 刘永定. 念珠藻葛仙米叶绿素荧光与水分胁迫的关系. 植物生理学通讯, 2000b, 36(3): 205-208.
李敦海, 宋立荣, 刘永定. 念珠藻葛仙米的藻殖段分化——信号转导参与过程的初步研究. 植物学通报, 2002, 19(3): 328-335.
李合生等. 植物生理生化实验原理和技术. 北京, 高等教育出版社, 2000.
凌裕泉, 屈建军, 胡玫. 沙面结皮形成与微环境变化.应用生态学报, 1993, 4(4): 393-398.
李守中, 肖洪浪等. 腾格里沙漠人工固沙植被区生物土壤结皮对降水的拦截作用. 中国沙漠, 2002, 22: 612-616.
刘永定, 黎尚豪. 长江中游黄棕壤地区几种稻田土壤的蓝藻种类及田间季节差异与垂直分布. 见: 廉正编. 长江流域资源、生态、环境与经济开发研究论文集. 1988, 北京: 科学出版社, 266-269.
刘永定, 黎尚豪. 土壤藻类及其生理生态. 水生生物学报, 1993, 17(3): 272-277.
刘永定, 沈银武, 宋立荣等. 黄河中游土壤类的种类组成与土壤肥力的关系. 水生生物学报, 1999, 23(5): 434-442.
李新荣, 贾玉奎, 龙利群等. 干旱半干旱地区土壤微生物结皮的生态学意义及若干研究进展. 中国沙漠, 2001, 21(1): 4-12.
李新荣, 张景光, 王新平等. 干旱沙漠区土壤微生物结皮及其对固沙植被影响的研究. 植物学报, 2000, 42(9): 965-970.
李运广, 高坤山. 盐胁迫对地木耳和葛仙米生理生化特性的影响. 水生生物学报, 2003, 27(3): 227-231.
吕贻忠, 杨佩国. 荒漠结皮对土壤水分状况的影响. 干旱区资源与环境, 2004, 18(2): 76-79.
贾宝全, 张红旗, 张志强, 慈龙骏. 甘肃省民勤沙区土壤结皮理化性质研究. 生态学报, 2003, 23(7): 1442-1448.
马红樱, 张德禄, 胡春香等. 植物活性多糖的研究进展. 西北师范大学学报(自然科学版), 2004, 40(3): 112-117.
缪锦来, 阚光锋, 李光友等. UV-B 辐照培养下南极冰藻的形态和超微结构及主要生化组成的变化. 中国海洋药物, 2003, 6: 1-5.
牛玉璐, 曹永胜. 生物结皮及其在荒漠治理中的作用. 生物学教学, 2005, 30(10): 5-6.
庞启深, 郭宝江, 阮继红. 螺旋藻多糖对核酸内切酶活性和 DNA 修复合成的增强作用. 遗传学报, 1988, 5: 374-381.
庞启深, 郭宝江, 阮继红. 螺旋藻抗辐射多糖的提纯和分析. 生物化学与生物物理学报, 1989, 21: 445-449.
尚玉昌. 普通生态学. 北京, 北京大学出版社, 2002.
王爱国, 邵从本, 罗广华. 丙二醛作为植物脂质过氧化指标的探讨. 植物生理学通讯, 1986, 2: 55-57.
王静. 地木耳改变土壤含氮肥量的研究. 兰州大学学报(自然科学版), 1995, 31( 3): 97-99.
魏培莲. 微生物胞外多糖研究进展. 浙江科技学院学报, 2002, 14(2): 8-12.
吴发启, 范文波. 坡耕地黄墡土结皮的理化性质分析. 水土保持通报, 2001, 21(4): 22-24.
吴楠, 潘伯荣, 张元明等. 古尔班通古特沙漠生物结皮中土壤微生物垂直分布特征. 应用与环境生物学报, 2005, 11 (3): 349～353.
吴楠, 潘伯荣, 张元明. 土壤微生物在生物结皮形成中的作用及生态学意义. 干旱区研究, 2004, 21(4): 444-450.
吴玉环, 高谦, 于兴华. 生物土壤结皮的分布影响因子及其监测. 生态学杂志, 2003, 22(3): 38-42.
杨晓辉, 张克斌, 赵石杰. 生物土壤结皮——荒漠化地区土壤研究的热点问题. 生态学报, 2001, 21(3): 474-480.
尤珊, 郑必胜, 郭祀远. 氮源对螺旋藻生长及胞外多糖的影响. 食品科学, 2004, 25(4): 32-35.
尤珊, 郑必胜, 郭祀远. 光照对螺旋藻形态及胞外多糖的影响和机理. 海湖盐与化工, 2004, 33(1): 23-25.
张丙昌, 张元明, 赵建成. 古尔班通古特沙漠生物结皮藻类的组成和生态分布研究. 西北植物学报, 2005, 25 (10): 2048-2055.
张大伟, 王艳, 蔡伟民. 沙尘暴源头控制的新思路. 上海环境科学, 2003, 增刊: 1-4.
张殿忠, 汪沛洪, 赵会贤. 测定小麦叶片游离脯氨酸含量的方法. 植物生理学通讯, 1990, 4: 62-65.
张光远, 蔡崇法. 黄绵土结皮的微形态特征及某此理化性质的研究. 见:中国—加拿大. 晋西黄土高原土壤侵蚀规律实验研究文集. 北京:水利电力出版社. 1990, 58-67.
张景钺, 梁家骥. 植物系统学. 北京: 人民教育出版社, 1978.
张继贤, 邸醒民, 王淑湘等. 沙坡头地区防护林体系建立过程中生态环境变化的特点. 干旱区资源与环境, 1994, 8(3): 68-79.
张利平. 天然吸附剂——壳聚糖的最新研究. 阴山学刊, 2001, 5: 42-44.
张维杰. 复合多糖生化研究技术. 上海: 上海科学技术出版社, 1987.
张元明, 曹同, 潘伯荣. 干旱与半干旱地区苔藓植物生态学研究综述. 生态学报, 2002, 22(7): 1129-1134.
赵吉, 邵土琴. 库布齐沙地土壤的生物学活性研究. 内蒙古大学学报(自然科学版), 1997, 28(5): 664-666.
赵玲, 尹平河等. 海洋赤潮生物原甲藻对重金属的富集机理. 环境科学, 2001, 22(4): 42-45.
郑有飞等. 紫外辐射增强对大豆影响的进一步分析. 环境科学学报, 1998, 18(5): 549-552.
钟泽璞, 施定基. 丝状体蓝藻藻殖段的分化及其调节机制. 植物学通报, 2000, 17(3): 204-210.
周礼恺. 土壤酶学. 北京: 科学出版社, 1987.
周志刚, 程子俊, 刘志礼. 沙漠结皮中藻类生态的研究. 生态学报, 1995, 15(4): 385-391.
周志刚, 刘志礼, 刘雪娴. 极大螺旋藻多糖的分离、纯化及其抗氧化特性的研究. 植物学报, 1997, 39: 77-81.
祝建, 王俊, 华振基等. 高压冷冻和低温替代技术制备的发菜营养细胞的超微结构. 植物学报, 1998, 40(10): 901-905.
Aguirre-von Wobeser E, Figueroa F L, Cabello-Pasini A. Effects of UV radiation on photoinhibition of marine macrophytes in culture systems. Appl. Phycol. 2000, 12: 159–168.
Ana O, Massimo V. Extracellular polysaccharide synthesis by Nostoc strains as affected by N source and light intensity. Journal of Biotechnology, 2003, 102: 143-152.
Andreas H, Cornelius L. Algae and UV irradiation: Effects on ultrastructure and related metabolic functions. Micron, 2006, 37: 190-207.
Angela H S, Dominic A H, Brendan J K. A critical assessment of the analysis and distributions of scytonemin and related UV screening pigments in sediments. Organic Geochemistry, 2004, 35: 1221-1228.
Angelova M, Petricheva E. Glucose- and nitrogen-dependence of acid proteinase production in semicontinuous culture with immobilized cells of Humicola lutea 120-5. Journal of Biotechnology, 1997, 58: 51–58
Araoz R, Háder D P. Ultraviolet radiation induces both degradation and synthesis of phycobilisomes in Nostoc sp. a spectroscopic and biochemical approach. FEMS Microbiol. Ecol., 1997, 23: 301-313.
Araoz R, Lebert M, Háder D P. Translation activity under ultraviolet radiation and temperature stress in the cyanobacterium Nostoc sp. J. Photochem. Photobiol. B Biol., 1998a, 47: 115-120.
Araoz R, Shelton M, Lebert M, et al. Differential behavior of two cyanobacteria species to UV radiation. Artificial UV radiation induces phycoerythrin synthesis. J. Photochem. Photobiol. B Biol., 1998b, 47: 175-183.
Arnotts T, Murphy T M. A comparison of the effects of a fungal elicitor and ultraviolet radiation on ion transport and hydrogen peroxide synthesis in rose cells. Environ Exp Bot, 1991, 31: 209-216.
Asthana R K, Chatterjee S, Singh S P. Investigations on nickel biosorption and its remobilization. Process Biochem, 1995, 30: 729–34.
Bailey D, Andrew P M, James R R. Aggregation of soil particles by algae. J. Phycol, 1973, 9, 99-101.
Baily D, Mazurak A P, Rosowski J R. Aggregation of soil particles by algae. Journal of Phycology, 1973, 9: 99-101.
Band C J, Arredondo-Vega B O, Vazquez-Duhalt R, et al. Effect of salt-osmotic upshock on the edaphic microalga Neochlaris oleoabundans. Plant Cell and Environment, 1992, 15: 129-133.
Banerjee M, Hader D P. Effects of UV radiation on the rice field cyanobacterium, Aulosira Fertilissima. Environmental Experimental Botany. 1996, 36(3): 281-291.)
Barbara N, Adriana P, Licia L, et al. Chemical composition and production of exopolysaccharides from representative members of heterocystous and non-heterocystous cyanobacteria. Phytochemistry, 1999, 52: 639-647.
Bell R A. Cryptoendolithic algae of hot semiarid lands and deserts. Journal of Phycology, 1993, 29: 133-139.
Belnap, Harper K T, Warren S D. Surface disturbance of cryptobiootic soil crusts: nitrogennase activity, chlorophyll content and chlorophyll degradation. Arid Soil Research and Rehabilitation, 1994, 8: 1-8.
Belnap J, Gardner J S. Soil microstructure in soils of the Colorado Plateau: the role of the cyanobadterium Microcoleus vaginatus. Great Basin Nat, 1993, 53: 40-47.
Belnap J, Gilletc D A. Vulnerability of desert biological soil crust to wind erosion: the influences of crust development, soil textuts and disturbance. Journal of Arid Environment, 1998, 39: 133-142.
Bennet A, Bogorad L. Complementary chromatic adaptation in a filamentous blue-green alga. J Cell Biol., 1973, 58: 419-435.
Biagini A B, Kirk K, Schofield P J, et al. Role of K+ and amino acids in osmoregulation by the free-living microaerophilic protozoon Hexamita inflata. Microbiol., 2000, 146: 427- 433.
Bilger W, Budel B. Photosynthetic activity of two developmental stages of a Nostoc strain (cyanobacteria) isolated from Ceosiphon pyriforne (Mycota). Phycol, 1994, 30: 225-230
Bloor S, England R R. Antibiotic production by the cyanobacterium Nostoc muscorum. J. Appl. Phyco., 1989, 1: 367-372.
Bold H C, Wynoc M J. Introduction to the Algae. PRENTICE-HALL, INC., London, 1978, 37-39.
Bongale U D. Distribution of Nostoc and Anabaena (Cyanophyta) in relation to soil propertiel in the cultivated soils of Karnataka state (India). Cryptogamie/Algologie, 1987, 8 (1): 13-18.
Booth W E. Algae as pioneers in plant succession and their importance in erosion control. Journal of Phycology, 1941, 11: 316-320.
Bothwell M L, Sherbot D, Pollock C M. Ecosystem response to solar ultraviolet-B radiation: Influence of trophic-level interactions. Science, 1994, 265: 97-100.
Bowler C, Montagu M V, Inze D. Superoxide dismutase and stress tolerance. Ann Rev Plant Physiol Plant Mol Biol., 1992, 43: 83-116.
Bradford M. A rapid and sensitive method for the quantification of microgram quantities of protein utilizing the principle of protein-dye binding. Anal. Biochem., 1976, 72: 248-254.
Bredt D S, Hwang P M, Glatt C E, et al. Cloned and expressed nitric oxide synthase structurally resembles cytochrome P-450 reductase. Nature, 1991, 351: 714-771.
Brenowitz S, Castenhol Z R W. Long-term effects of UV and visible irradiance on natural population of a scytonemin-containing cyanobacterium (Calothirix sp.). FEMS Microbiol Ecol., 1997, 24: 343-352.
Britt A B. Repair of DNA damage induced by ultraviolet radiation. Plant Physiol., 1995, 108: 891-896.
Broady P A. Taxonomic and ecological investigations of algae on steam-warmed soil on Mt Erebus Ross Island, Antarctica. Phycologia, 1984, 23(3): 257-271.
Caiola M G, Daniela B, Friedmann E I. Effect of desiccation on envelopes of the cyanobacterium Chrococcidicpsis sp. (Chroococcales). Eur. J. Phycol, 1996, 31: 97-105.
Caire G Z, Cano M S, Mulé M C Z, et al. Action of cell-free extracts and extracellular products of Notoc muscorum on growth of Sclerotinia sclerotiorum. Phyton, 1987, 47: 43-36.
Caire G Z, Cano M S, Mulé M C Z, Halperin D R. Antimycotic products from the cyanobacterium Nostoc muscorum against Rhizoctonia solani. Phyton, 1990, 51: 1-4.
Campbell D, Eriksson S M J, Oquist G, et al. The cyanobacterium Synechococcus resists UV-B by exchanging photosystem Ⅱ reaction-center D1 proteins. Proc. Natl. Acad. Sci. USA, 1998, 95: 364-369.
Campbell S E. Soil stabilization by a prokaryotic desert crust: implications for precambrian land biota. Origins of life, 1979, 9: 335-348.
Castenholz R W. Multiple strategies for UV tolerance in cyanobacteria. Spectrum, 1997, 10: 10-16.
Castenholz R W, Garcia-Pichel F. Cyanobacterial responses to UV radiation. Whitton B A, Pottsm, eds. The ecology of cyanobacteria: their diversity in time and space. Kluwer Academic Publishers, 2000: 591-611.
Castenholz R W, Waterbury J B. Cyanobacteria. In: Bergey’s Manual of Systematic
Bacteriology (Staley, J.T., Bryant, M.P., Pfenning, N. and Holt, J.G., Eds.), 1989, Vol. 3, pp. 1710-1799. Williams and Wilkins, Baltimore, MD.
Chen L Z, Li D H, Liu Y D. Salt tolerance of Microcoleus vaginatus Gom., a cyanobacterium isolated from desert algal crust, was enhanced by exogenous carbohydrates. Journal of Arid Environments, 2003, 55: 645–656.
Chu H J, Tsang C T. Research and utilization of cyanobacteria in China: a report. Arch. Hydrobiol. Suppl. 1988, 80: 1-4.
Cockell C S, Knowland J. Ultraviolet radiation screening compounds. Biol. Rev., 1999, 74: 311-345.
Conde F R, Churiom S, Previtali C M. The photoprotector mechanism of mycosporine-like amino acids. Excited-state properties and photostability of porphyra-334 in aqueous solution. J. Photochem. Photobiol. B Biol., 2000, 56: 139-144.
Correia C M, Arealelv, Torres-Pereira M S, et al. Intraspecific variation in sensitivity to ultraviolet-B radiation in maize grown under field conditions. I. growth and morphological aspects. Field Crops Research, 1998, 59: 81-89.
Costerton J W, Irvin R T, Cheng K J. The bacterial glycocalyx in nature and disease. Annu.Rev. Microbiol, 1981, 35: 299-324.
Crutzen P J. Ultraviolet on the increase. Nature, 1992, 356: 104-105. Davey M C, Clarke K J. Fine structure of a terrestrial cyanobacterial mat from Antarctica. J Phycol, 1992, 28: 199-202.
Dillon J G, Tatsumicm, Tandingan P G, et al. Effect of environmental factors on the synthesis of scytonemin a UV-screening pigment, in a cyanobaterium (Chroococcidiopsis sp.). Arch. Microbiol., 2002, 177: 322-331.
Doanhue B A, Taylor J S, Reinesd. Transcript cleavage by RNA Polymerase (2) arrested by acyclobutane dimmer in the DNA template. Proc. Natl. Acad. Sci. USA., 1994, 91: 8502-8506.
Doers M, Parker D L. Properties of Microcystis aeruginosa and M. flos-aquae (Cyanophyta) in culture. J Phycol, 1988, 24: 502–8.
Dohler G, Hagmeier E, David C H. Effect of solar and artificial UV irradiation on pigments and assimilation of 15N ammonium 15N nitrate by macroalgae. J. Photochem. Photobiol. B Biol., 1995, 30: 179-187.
Domenico V, Herlinda G V, Gabriel C. Nitrogen removal and recycling by Scenedesmus obliquus in semicontinuous cultures using artificial wastewater and a simulated light and temperature cycle. Bioresource Technology, 2005, 96: 359-362.
Donkor V, Káder D P. Effects of solar and ultraviolet radiation on motility, photomovement and pigmentation in filamentous, gliding cyanobacteria. FEMS Microbiol. Ecol., 1991, 86: 159-168.
Durrell L W, Shields L W. Characteristics of soil algae relation to crust formation. Trans. Am.Microbiol. Soc, 1961, 80(1): 73-79.
Eldridge D T, Greene R S B. Microbiotic soil crusts: a review of their roles in soil and ecological processes in the rangelands of Australia. Australian Journal of Soil Research, 1994a, 32: 389-415.
Eldridge D T, Greene R S B. The effect of time since fire on the cover and composition of cryptogamic soil crusts on an Encalypus shrubland soil. Cunninghamia, 1994b, 3: 581-599.
Enlings M. UV-B induced synthesis of photoprotective pigments and extracellular polysaccharides in terrestrial cyanobaterium Nostoc commune. Bacteriol, 1997, 179(6): 1940.
Farman J C, Gard N B G, Shan K J D. Large losses of total ozone in Antarctica reveal seasonal CLOx/NOx. Nature, 1985, 315: 207-210.
Farooq M, Suresh B G, Ray R S, Misra R B, Shanker U, Hans R K. Sensitivity of duckweed (Lemna major) to ultraviolet-B radiation. Biochem. Biophys. Res. Commun. 2000, 276: 970–973.
Farooq M, Shankar U, Ray R S, Misra R B, Agrawal N, Verma K, Hans R K. Morphological and metabolic alterations in duckweed (Spirodela polyrhiza) on long-term low-level chronic UV-B exposure. Ecotoxicology and Environmental Safety, 2005, 62: 408-414.
Fauchot J, Gosselin M. Influence of UV-B radiation on nitrogen utilization by a natural assemblage of phytoplankton. J. Phycol., 2000, 36: 484-496.
Ferran G P, Richard W, Castenholz. Characterization and biological implications of scytonemin, a cyanobacteria sheath pigment. J. Phycol., 1991, 27: 395-409.
Foyer C. Photosynthesis. New York: John Wiley and Sons Inc, 1984, 60-70.
Frantz G. Polysaccharides in pharmacy: current applications and future concepts. Planta Med, 1989, 55: 493–7.
Friedmann E I, Hua M, Ocampo-Friedmann J A. Crpytoendolithic lichen and cyanobacterial microbial community of the Ross Desert. Polarforschung, 1988, 58: 251-259.
Friedmann E I, Ocampo-Friedmann R. A primitive cyanobacterium as pioneer microorganism for terraforming Mars. Adv. Space Res, 1995, 15(3): 243-246.
Frisog, Speteac, Giacomettigm. Degradation of photosystem Ⅱ reaction center D1 polypeptide induced by UV-B radiation in isolated thylakoids. Identification and characterization of C- and N-terminal breakdown products. Biochim. Biophys. Acta, 1994, 1184: 78- 84.
Gadd G M. Heavy metal accumulation by bacteria and other microorganisms. Experientia, 1990, 46: 834–42.
Garcia-Pichel F, Belnap J. Microenvironments and microscale productivity of cyanobacterial desert crusts. J. Phycol, 1996, 32: 774–782.
Gerhardt K E, Wilson M I, Greenberg B M. Ultraviolet wavelength dependence of photomorphological and photosynthetic responses in Brassica napus and Arabidopsis thaliana. Photochem. Photobiol. 2004.
Giannopotitis C N, Ries S K. Superoxide dismutase in higher plants. Plant Physiology, 1977, 59: 309-314.
Gotz T, Whidhovel U, Boger P, et al. Protection of photosynthesis against ultraviolet-B radiation by carotenoids in transformants of the cyanobacterium Synechococcus PCC 7942. Plant Physiol., 1999, 120: 599-604.
Gourr K, Pandey P K, Bisen P S. Differential response in damage and repair of wild-type Anacystis nidulans and its UV-B plus heat shock tolerant (UV-HSt) strain under UV-B and heat shock stress. J. Photochem. Photobiol. B Biol., 1997, 40: 61- 67.
Greene R S B, Chanres C J. The effect of fire on the soil and the degraded semiarid woodland. Cryptogam cover and physiea microphological properties. Australian J soil Res., 1990, 755-777.
Gromov B V, Vepritskiy A A, Titova N N, et al. Production of the antibiotic cyanobacterin LU-1 by Nostoc linckia CALU 892 (cyanobacterium). J. Appl. Phycol. 1991, 3: 55-59.
Gupta V V S R, Germida J J. Distribution of microbial biomass and its activity in soil aggregate size classes as affected by cultivation. Soil Biol Biochem, 1988, 20: 777-786.
Güven K C, Ozsoy Y, Ulutin O N. Anticoagulant, fibrinolytic and antiaggregant activity of carrageenans and alginic acid. Bot Mar, 1991, 34: 429–432.
Hall D O, Rao K K. Photosynthesis (Fourth Edition), Edward Arnold, London, 1987: 18-23.
Harper K T, Marble J R. A role for nonvascular plants in management of arid and semiarid rangeland. In: Tueller P T. (ed).Vegetation Science Applications for Rangeland Analysis and Management. Dordrecht: Kluwer Academic Publisher, 1988, 135-169.
Hellebust J A. Mechanisms of response to salinity in halotolerant microalgae.Plant and Soil, 1985, 89: 69-81.
Hernando M P, Ferreyra G A. The effects of UV radiation on photosynthesis in an Antarctic diatom (Thalassiosira sp.): Does vertical mixing matter? Journal of Experimental Marine Biology and Ecology, 2005, 325: 35-45.
He Y Y, Háder D P. Involvement of reactive oxygen species in the UV-B damage to the cyanobacterium Anabaena sp.. J. Photochem. Photobiol. B Boil., 2002a, 66: 73-80.
He Y Y, Háder D P. UV-B-induced formation of reactive oxygen species and oxidative damage of the cyanobacterium Anabaena sp.: protective effects of ascorbic acid and N-acetyl-L-cysteine. J. Photochem. Photobiol. B Boil., 2002b, 66: 115-124.
Hidege, Vassi. UV-B induced free radical production in plant leaves and isolated thoylakoid membranes. Plant Sci., 1996, 115: 251-260.
Hill D R, Keenan T W, Helm R F, et al. Extracellular polysaccharide of Nostoc commune (cyanobacteria) inhibits fusion of membrane vesicles during desiccation. J. Applied. Phycol., 1997, 9: 237-248.
Holm-Hansen O, Helbling G W, Lubin D. Ultraviolet radiation in Antarctica: inhibition of primary production. Photochem. Photobiol, 1993, 58: 567– 570.
Hoppe H A. Marine algae and their products and constituents in pharmacy. In Hoppe, H.A, Levring & T. Tanaka, Y. [Eds.] Marine Algae in pharmaceutical Science. Walter de Gruyter, Berlin, 1979, 1: 25-119.
Hori K, Ishibashi G, Okita T. Hypocholesterolemic effect of blue-green alga ishikurage (Nostoc commune) in rats fed atherogenic diet. Plant Foods Hum. Nutr, 1994, 45: 63～70.
Hpknal, Bondma, Tobnak. Effects of UV-B on the development and ultrastructure of the primary leaf of wheat (Triticum aestivum). J. Exp. Bot., 1996, 47(sup): 20.
Huang Z B, Liu Y D, et al. Studies on polysaccharides from three edible species of Nostoc (cyanobacteria) with different colony morphologies: comparison of monosaccharide compositions and viscosities of polysaccharides from field colonies and suspension cultures. J. Phycol, 1998, 34: 962–968.
Hu C X, Liu Y D, Song L R, Zhang D L. Effect of desert soil algae on the stabilization of fine sands. Journal of Applied Phycology, 2002a, 14: 281-292.
Hu C X, Liu Y D, Zhang D L, Huang Z B, Paulsen B S. Cementing mechanism of algal crusts from desert area. Chin Sci Bull, 2002b, 47: 1361-1368
Hu C X, Liu Y D, et al. Extracellular carbohydrate polymers from five desert soil algae with different cohesion in the stabilization of fine sand grain. Carbohydrate Polymers, 2003a, 54: 33-42.
Hu C X, Liu Y D. Primary succession of algae community structure in desert soil. Acta Botanica Sinica, 2003, 45 (8): 917-924.
Hu C X, Zhang D L, Huang Z B, Liu Y D. The vertical microdistribution of cyanobacteria and green algae within desert crusts and the development of the algal crusts. Plant and Soil, 2003c, 257: 97-111.
Huheihel M, Ishanu V, Tal J, Arad A. Activity of Porphyridium sp. polysaccharides against Herpex simplex viruses in vitro and in vivo. J. Biochem. Biophys. Methods, 2001, 50: 189-200.
Itoh H, Noda H, Amano H, Zhuaug C, Mizuno T, Ito H. Antitumor activity and immunological properties of marine algal polysaccharides, specially fucoidan, prepared from Sargassum thunbergii of Phaeophyceae. Anticancer Res., 1993, 13: 2045-2052.
Jansen M A K, Noort V D, Tan M Y, et al. Phenol-oxidizing peroxidases contribute to the protection of plant from ultraviolet radiation stress. Plant Physiol, 2001, 126: 1012-1023.
Janssen L H J, Hasselt. Temperature-induced alterations of in vivo chlorophyll a fluorescence in cucumber as affected by DCMU. Photosynth Res., 1988, 15: 153-162.
Jarman T R, Deavin L, Slocombe S, Rhighelato R C. Investigation of the effect of environmental conditions on the rate of exopolysaccharide synthesis in Azotobacter vinelandii. J. Gen. Microbiol., 1978, 107: 59–64.
Johansen J R. Cryptogamic crusts of semiarid and arid lands of North America. J Phycol, 1993, 29: 140.
Johnston H S. Reduction of stratospheric ozone by nitrogen oxide catalysts from supersonic transport exhaust. Science, 1971, 173: 517-522.
Jordan B R, James P E, Mackerness S A H. Factors affecting UV-B induced changes in arabiodopsis thaiana L. gene expression: the role of development protective pigments and the chloroplast signal. Plant Cell Physiol, 1998, 39 (7): 769-778.
José M, ángeles V, et al. Exopolysaccharide production by the cyanobacterium Anabaena sp. ATCC 33047 in batch and continuous culture. Journal of Biotechnology, 1998, 60: 175-182
José M, ángeles V, et al. Outdoor cultivation of a nitrogen-fixing marine cyanobacterium, Anabaena sp. ATCC 33047. Biomolecular Engineering, 2003, 20: 191-197.
Kaplan D, Christiaen D, Arad S M. Binding of heavy metals by algal polysaccharides. In Stadler T, Mallion J, Verdus M C, Karamanos Y, Morvan H, Christiaen D. (Eds.) Algal Biotechnology. Elaevier Applied Science, London and New York, 1988, 179-187.
Karentz D, Ceaver J E, Mitchell D L. DNA damage in the Antarctic. Nature, 1991, 350: 28.
Karentz D, et al. Impact of UV-B radiation on pelagic freshwater ecosystems: Report of working group on bacteria and phytoplankton. Arch. Hydrobiol, 1994, 43: 31-69.
Kennedy J F, White C A. Bioactive Carbohydrates in Chemistry, Biochemistry and Biology. Ellis Horwood Ltd., Chichester, England, 1983.
Kidron G J, Barzilay E, Sachs E. Microclimate control upon sand microbiotic crust, western Negev Desert, Israel. Geomorphology, 2000, 36: 1-18.
Kollib, Tiwaris, Mohantyp. Ultraviolet-B induced damage to photosystem Ⅱ in intact filaments of Spirulina platensis. Nature, 1998, 53: 369- 377.
Kramer G F, Norman H A, Krizek, et al. Influence of UV-B radiation on polyamines, lipid peroxidation and membrane lipids in cucumber. Phytochemistry, 1991, 30 (7): 2101-2108.
Krause G H, Weis E. Chlorophyll fluorescence as a toll in plant physiology. Ⅱ. Interpretation of fluorescence signals. Photosybthesis Res., 1984, 5: 139-157.
Kumar A, Sinha R P, Háder D P. Effect of UV-B on enzymes of nitrogen metabolism in the radiation in the cyanobacterium Nostoc calcicola. J. Plant Physiol., 1996, 148: 86-91.
Kumar A, Tyagim B, Jhapn, et al. Inactivation of cyanobacterial nitrogenase after exposure to ultraviolet-B radiation. Curr. Microbiol., 2003, 46: 380-384.
Lange O L, Meyer A, Zellner H. Photosynthesis and water relation of lichen soil crusts: field measurements in the coastal fog zone of the Namib Desert. Functional Ecology, 1994, 8: 253-264.
Lao K Q, Alexander N G. Ultraviolet-B photodestruction of a light-harvesting complex. Proc. Natl. Acad. Sci. USA., 1996, 93: 5258-5263.
Leavitt P R. A review of factors that regulate carotenoid and chlorophyll deposition and fossil pigment abundance. J. Paleolimnol. 1993, 9: 109-127.
Leys J F. Coverlevels to control soil and nutrient loss from wind erosion on sand plain country in central N.S.W.Proc. 7th Biennial Conference of the Aust. Rangel. Soc. Cobar, 1992, 84-91.
Leys J F. Soil crusts, their effect on wind erosion. Soil Conservation service of N.S.W. Research Note, 1990.
Li X R, Zhang J G, Wang X P, et al. Study on soil microbiotic crust and its influences on sand-fixing vegetation in arid desert region. Acta Botanica Sinica, 2002, 42(9): 965- 970.
Liu H, Buskey E J. Hyper salinity enhances the production of extracellular polymeric substance (EPS) in the texas brown tide alga, Aureoumbra Lagunensis (Pelagophyceae) . J. Phycol., 2000, 36: 71-77.
Liu Y D & Li S H. Species composition and vertical distribution of blue-green algae in rice field soil, Hubei, China. Nova Hedwigia, 1989, 48: 55-67.
Liu Y D, Shen Y W, Song L R, et al. Species composition and distribution of blue-green algae from soil in the middle reach of Yellow River, China. Proceeding of international conference on Asian Network on microbial researches, 1998, 395-401.
Lukesova A. Soil algae in four secondary successional stages on abandoned fields. Algological Studies, 1993, 71: 81-102.
Lynch J M, Bragg E. Microorganisms and soil aggregate stability. Advances in Soil Science, 1985, 2: 133-171.
Lynch J M. Interactions between biological processes, cultivation and soil structure. Plant Soil, 1984, 76: 307-318.
Mackerness A H, John C F, Jordan B, et al. Early signaling components in ultraviolet-B responses: distinct roles for different reactive oxygen species and nitric oxide. FEBS lett, 2001, 489 (2): 237-242
Mackerness A H, Jordon B R, Thoma S B. Reactive oxygen species in the regulation of photosynthetic genes by ultraviolet-B radiation in green and etiolated buds of pea (Pisum sativum L.). J. Photochem. Photobiol. B Boil., 1999, 48: 180-188.
Mackerness A H. The effect of supplemental ultraviolet-B radiation on mRNA transcripts, translation and stability of chloroplast proteins and pigment formation in Pisum sativum L. J. Exp Bot, 1997, 48: 729-738.
Malanga G, Puntarulo S. Oxidative stress and antioxidant content in Chlorellavulgaris after exposure to ultraviolet-B radiation. J Physiologia Plantarum, 1995, 94: 672-679.
Mata L, Silva J, Schuenhoff A, Santos R. The effects of light and temperature on the photosynthesis of the Asparagopsis armata tetrasporophyte (Falkenbergia rufolanosa), cultivated in tanks. Aquaculture, 2006, 252: 12-19.
MáTé Z, Sass L, Szekeresm, et al. UV-B induced differential transcription of psbA genes encoding the D1 protein of photosystem Ⅱ in the cyanobacterium Synechocystis 6803. J. Biol. Chem., 1998, 273: 17439-17444.
Mazor G, Kidron G J, Vonshak A, Abeliovich A. The role of cyanobacterial exopolysaccharides in structuring desert microbial crusts. FEMS Microbiology Ecology, 1996, 21: 121-130.
Mehta V B & Vaidya B S. Cellular and extracelluar polysaccharides of the blue-green alga Nostoc. J. Exp. Bot. 1978,29: 1423-1430.
Metting B. The systematic and ecology of soil algae. The Bot. Rev., 1981, 47(2): 195-312.
Monika E S, Wolfgang B, Ssiegfried S. UV-B-induced synthesis of photoprotective pigments and extracellular polysaccharides in the terrestrial cyanobacterium Nostoc commune. J. Bac. Mar., 1997, 179: 1940-1945.
Murphy T M. Effect of broad-band ultraviolet and visble radiation in hydrogen peroxide formation by cultured rose cells. Physiol. plant, 1990, 80: 63-78.
N?geli C. Gattungen einzelliger Algen, physiologisch and systematisch bearbeitet, Neue Denkschrift, Allg. Schweiz. Natur Ges. 1849, 10: 1-138.
Noctor G, Foyer C H. Ascorbate and glutathione: Keeping active oxygen under control. Annual Review of Plant Physiology and Plant Molecular Biology, 1998, 49: 249-279.
Pang Q S, Guo B J & Ada K. Radioprotective effect of extract from Spirulina platensis in mouse bone marrow cells studied by using the micronucleus text. Toxico. Let., 1989,48: 165-169.
Patterson G. Antiviral activity of cultured blue-green algae (Cyanophyta). J. Phycol. 1993, 29: 125~130.
Peter R L, Rolf D V, David B D, John P S, David W S. Past ultraviolet radiation environments in lakes derived from fossil pigments. Nature, 1997, 388: 457- 459.
Peterson J B. Studies on the biology and taxonomy of soil algae. Dansk Botanisk Arkiv, 1935, 8(9): 8-70.
Pintome, Casatip, Hsutp, et al. Effects of UV-B radiation on growth, photosynthesis, UV-B-absorbing compounds and NADP-malic enzyme in bean (Phaseolus vulgaris L.) grown under different nitrogen conditions. J. Photochem. Photobiol. B Biol., 1999, 48: 200-209.
Portwich A, Garcia P F. Ultraviolet and osmotic stresses induce and regulate the synthesis of mycosporines in the cyanobacterium Chlorogloeopsis PCC 6912. Arch. Microbiol., 1999, 172: 187-192.
Potts M. Chroococcus S24 and Chroococcus N41(cyanobacteria): morphological, biochemical and genetic characterization and effects of water stress on ultrastructure. Arch Microbiol, 1983,135: 81-90.
Potts M. Minireview: Mechanisms of desiccation tolerance in cyamobacteria. Eur. J. Phycol., 34: 319-328.
Prabha G L, Kulandaivelu G. Induced UV-B resistance against photosynthesis damage by adaptive mutagenesis in Synechococcus PCC 7924. Plant Sci., 2002, 162: 663-669.
Preusss B, Britta B. A DNA-damage-induced cell cycle checkpoint in Arabidopsis. Genetics, 2003, 164: 323- 334.
Prosperi C. Environmental factors affecting in vitro nitrogenase activity of cyanobacteria isolated from rice-fields. J. Applied. Phycol, 1992, 4: 197-204.
Proteau P J, Gerwick W H, Garcia P, Castenholz R W. The structure of scytonemin, an ultraviolet sunscreen pigment from the sheaths of cyanobacteria. Experientia, 1993, 49: 825-829.
Quaite F E. DNA damage levels setermine cyclobutyl pyrimidine dimer repair mechanisms in alfalfa seedings. Plant Cell, 1994, 6: 1635-1641.
Quaite F E, Sueherland B M, Sutherland J C. Action spectrum for DNA damage in alfalfa lowers predicted impact of ozone depletion. Nature, 1992, 358: 576- 578.
Rail C. Interactive effects of UV-B and copper on photosynthetic activity of the cyanobacterium Anabaena doliolum. Environ Exp Bot, 1995, 35(2): 177.
Rajapopal S, Murthysd D, Mohanty P. Effect of ultraviolet-B radiation on intact cells of the cyanobacterium Spirulina platensis characterization of the alteration in the thylakiod membranes. J. Photochem. Photobiol. B Boil., 2000, 54: 61- 66. Rao AV, Venkatesward. Microbial ecology of the soil of Indian Desert. Agri Ecosyst & Environ, 1983, 10(4): 498～513.
Rao M V, Palivath G, Ormrod D P. Ultraviolet-B and ozone-induced biochemical changes in antioxidant enzymes of A rabidopsis thaliana. Plant Physiol, 1996, 110: 125-136.
Reddy K J, Soper B W, Tang J, Bradley R L. Phenotypic variation in exopolysaccharide production in the marine, aerobic nitrogen-cxing unicellular cyanobacterium Cyanothece sp. World J. Microbiol. Biotechnol. 1996,12: 311-318.
Rippka R, Deruelles J W J B, Herdman M, Stanier R Y. Generic assignments, strain histories and properties of pure cultures of cyanobacteria. J Gen Microbiol, 1979, 111: 1-61.
Roberto D P, Massimo V. Outermost polysaccharidic investments of cyanobacteria: Nature, significance and possible applications. Recent Res. Devel. Microbiology, 2003b, 7: 13-22.
Roberto D P, Raffaella P, et al. Assessment of the metal removal capability of two capsulated cyanobacteria, Cyanospira capsulata and Nostoc PCC7936. Journal of Applied Phycology, 2003a, 15: 155-161.
Roberto D P, Vincenzini M. Exocellular polysaccharides from cyanobacteria and their possible applications. FEMS Microbiol Rev, 1998, 22: 151–75.
Rómulo A, H?der D P. Ultraviolet radiation induces both degradation and synthesis of phycobilisomes in Nostoc sp.: a spectroscopic and biochemical approach. FEMS Microbiology Ecology, 1997, 23: 301-313.
Rousseaux M C, Julkunen T R, Searles P S, Scopel A S, Aphalo P J, Ballarc C L. Solar UV-B radiation affects leaf quality and insect herbivory in the southern beach tree Nothofagus antartica. Oecologia, 2004, 38 (4): 505–512.
Sandmann G, Kuhn S, Boger P. Evaluation of structurally different carotenoids in Escherichia coli transformants as protectants against UV-B radiation. Appl. Environ. Microbiol., 1998, 64: 1972-1974.
Sauter M, Seagull R W, Kende H. Internodal elongation and orientation of cellose microfibrils and microtubules in deepwater rice. Planta, 1993, 190: 354-362.
Savory A. Holistic resource management. Island Press, Covelo California, 1988,564. Scherer S. Recovery of adenine-nucleotide pools in terrestrial blue-green algae after prolong drought periods. Oecologia, 1986, 68: 585-588.
Scherer S, Chen T W, Boger P. A new UV-A/B protecting pigment in the terrestrial cyanobacterium Nostoc commune. Plant Physial.,1988, 88: 1055-1057.
Scherer S, Potts M. Novel water stress- protein from a desiccation-tolerant cyanobacterium.J. Biol. Chem., 1989, 264(21): 12546-12553.
Schindler D W, Curtis J P, Parker B R, Stainton M P. Consequences of climate warming and lake acidification for UV-B penetration in North American boreal lakes. Nature 1996, 379: 705-708.
Schulten J A. Soil aggregation by cryptogams of a sand prairie. J Bot, 1985, 72(11): 1657-1661.
Shalata A, Tal M. The effect of salt stress on lipid peroxidation and antioxidants in the leaf of the cultivated tomato and its wild salt-tolerant relative Lycopersicon pennellii. Physiol. Plant, 1998, 104: 167-174.
Shao Y Q, Zhao J. Study on soil microbial number and soil ecological factor in fixed dunes in the east Hobq sands of NeiMongol. Acta Sci Nat Univ NeiMongol (Nat Sci), 1997, 28 (5): 715-719.
Shibata K. Pigments and a UV-absorbing substance in corals and a blue-green alga living on the Great Barrier Reef. Plant Cell Physiol, 1969, 10: 325-335.
Shields L M, Durrell L W. Algae in relation to soil fertility. Bot. Rev., 1964, 30(1): 92-128.
Siebeck O, et al. Impact of UV-B radiation on zooplankton and fish in pelagic freshwater ecosystems. Arch. Hydrobiol. 1994, 43: 101-114.
Singh N, Asthana R K, Kayastha A M, Pandey S, Chaudhary A K, Singh S P. Thiol and exopolysaccharide production in a cyanobacterium under heavy metal stress. Process Biochemistry, 1999, 35: 63–68.
Sinha R P, Klisch M, Gr?niger A, H?der D P. Ultroviolet-absorbing/screening in cyanobacteria, phytoplankton and macroalgae. J. Photochem. Photobiol. B: Biol, 1998, 47: 82-94.
Sinha R P, Kumar H D, Kumar A, Háder D P. Effects of UV-B irradiation on growth, survival, pigmentation and nitrogen metabolism enzymes in cyanobacteria. Acta Protozool, 1995, 34: 187-192.
Sinha R P, Lebert M, Kumar A, et al. Distintegration of phycobilisomes in a rice field cyanobacterium Nostoc sp. following UV irradiation. J. Photochem. Photobiol. B Boil., 1995, 37(4): 697-706.
Sinha R P, Singh N, Kumar A, et al. Effects of UV irradiation on certain physiological and biochemical processes in cyanobacteria. J. Photochem. Photobiol. B Biol., 1996, 32: 107-113.
Sinha R P, Sinha J P, Groniger A, et al. Polychromatic action spectrum for the induction of a mycosporine-like aminoacid in a rice-field cyanobacterium, Anabaena sp.. J. Photochem. Photobiol. B Biol., 2002, 66: 47-53.
Skarpe C & Henriksson E. Nitrogen fixation by cyanobacterial crusts and by associative-symbiotic bacteria in Western Kalahari, Botswana. Arid Soil Res & Rehabilitation, 1986, 1: 55～59.
Smith D W & Brock T D. The water relations of the alga Cyanidium caldarium in Soil. J. Gen. Microbiol., 1973,127: 74-78.
Smith R C, Prézelin B B, et al. Ozone depletion: ultraviolet radiation and phytoplankton biology in Antarctic waters. Science, 1992, 255: 952-959.
Solheim B, Johanson U, Callaghan T V, et al. The nitrogen fixation potential of arctic cryptogram species is influenced by enhanced UV-B radiation. Oecologia, 2002, 133: 90-93.
Speteac, Hidege, Vassi. The quinone electron acceptors are not the main sensitizers of UV-B induced protein damage in isolated photosystem Ⅱ reaction center and core complexes. Plant Sci., 1996, 115: 207-215.
Stolarski R, Bojkov R, Bishop L. Measured trends in stratospheric ozone. Science, 1992, 56: 342-349.
Strid A. Alteration in expression of defence genes in Pisum sativum after exposure to supplementary ultraviolet-B radiation. Plant Cell Physiol, 1993, 34: 949-953.
Strid A. Alteration in pigment content in leaves of Pisum sativum after exposure to supplementary UV-B. Plant Cell Physiol, 1992, 33 (7): 1015-1023.
Sullivan J H. Effects of increasing UV-B radiation and atmospheric CO2 on photosynthesis and growth: implications for terrestrial ecosystems. Plant ecology, 1997,128: 194-206.
Suresh B G, Joshi P C, Viswanathan P N. UV-B induced reduction in biomass and overall productivity of cyanobacteria. Biochem. Biophys. Res. Commun. 1998, 244: 138-142.
Takeuchia, Yamaguchit, Hidemaj, et al. Changes in synthesis and degradation of Rubisco and LHC Ⅱ with leaf age in rice (Oriza sativa L.) growing under supplementary UV-B radiation. Plant Cell Environ., 2002, 25: 695-706.
Takeuchi Y, Akizuki M, Shimizu H, Kondo N, Sugahara K. Effect of UV-B (290–320 nm) irradiation on growth and metabolism of Cucumber cotyledons. Physiol. Plant. 1989, 76: 425-430.
Takeuchi Y, Kubo H, Kasahara H, et al. Adaptive alteration in activities of scavengers of active oxygen in cucumber cotyledons irradiated with UV-B. J. Plant Physiol, 1996, 147(5): 589-592.
Tchan Y T, Whitehouse J N A. Study of soil algae II. The variation of the soil algal population in sandy soils. Proc. Linn. Soc. New. South Wales, 1953, 78: 160-170.
Tevinim, Iwanzikw, Thomav. Some effects of enhanced UV-B irradiation the growth and composition of plants. Planta, 1981, 153: 388-394.
Tevinim, Teramura A H. UV-B effects on terrestrial plants. Photochem Photobiol, 1989, 50: 479-487.
Tiano P, Accolla P, Tomaselli L. Phototrophic biodeteriogens on lithoid surfaces: An ecological study. Microbiol. Ecol., 1995, 29: 299-309.
Tyagi R, Kumar A, Tyagim B, et al. Protective role of certain chemicals against UV-B-induced damage in the nitrogen-fixing cyanobacterium, Nostoc muscorum. J. Basic Microbiol., 2003, 43: 137-147.
Vaidya B S, Mehta V. Carbohydrates in some blue-green algae. Phykos, 1989, 28: 89-100.
Vassi, Turcsányi, Toulou P, et al. The mechanism of UV-A radiation-induced inhibition of photosystem Ⅱ electron transport studied by EPR and chlorophyll fluorescence. Biochem., 2002, 41: 10200-10208.
Vonshak A, Torzillo G & Tomaseli L. Use of chlorophyll fluorescence to estimate the effect of photoinhibition in outdoor cultures of Spirulina platensis. J Appl Phycol., 1994, 6: 31-34.
Vu C V, Allen L H, Garrard L A. Effects of ebgabced UV-B radiation (280～320 nm) on ribulise-1, 5-bisphos-phate carboxylase in pea and soy bean. Environ Exp Bot, 1983, 23: 150-156.
West N E. Structure and function of microphytic soil crusts in wildland ecosystems of arid to semiarid regions. Advances in Ecological Research, 1990, 20: 179-223.
Willekens H, Vancam P, Vanmontagum, et al. Ozone, sulphur dioxide and UV-B radiation have similar effects on mRNA accumulation of antioxid antgenes in Nicotiana plumbag inifolia L. Plant Physiol, 1994, 106: 1007-1014.
Wingender J, Neu T R, Flemming H C. What are bacterial extracellular polymeric substances? In Wingender J. Neu TR, Flemming H-C (eds), Microbial Extracellular Polymeric Substances. Springer, Berlin. 1999, 1-19.
Wintermans J F G M, Mots D A. Spectrophotometric characteristics of chlorophylls a and b and their pheophytins in ethanol. Biochem Biophys Acta, 1965, 109: 448-453.
Woodall A A, Britton G, Jackson M J. Carotenoids and protection of phospholipids in solution or in liposomes against oxidation by peroxyl radicals: relationship between carotenoid structure and protective ability. Biochim. Biophys. Acta, 1997, 1336: 575-586.
Yan N D, Keller W, Scully N M, Lean D R S, Dillon P. Increased UV-B penetration in a lake owing to drought-induced acidification. Nature, 1996, 381: 141-143.
Yuichi T, Akizuki M, Shimizu H, Kondo N, Sugahara K. Effect of UV-B (290-320 nm) irradiation on growth and metabolism of cucumber cotyledons. Physiol. Plant, 1989, 76: 425-430.
Zaady E, Groffman P, Shachak M. Nitrogen fixation in macro– and microphytic patches in the Negev Desert. Soil B iol & B iochem, 1998, 30: 449-454.
Zak D R, Tilman D. Plant production and soil microorganisms in alter succession ecosystems: a continental-scale study. Ecology, 1994, 75(8): 2333-2347.
Zhang Q, Li N, Zhou G, Lu X, Xu Z, Li Z. In vivo antioxidant activity of polysaccharide fraction from Porphyra haitanesis (Rhodephyta) in aging mice. Pharmacol Res 2003, 48(2): 151-155.
Zhou G F, Sheng W X, Yao W H, Wang C H. Effect of low molecular λ-carrageenan from Chondrus ocellatus on antitumor H-22 activity of 5-Fu. Pharmacological Research, 2006, 53: 129-134.
Ziska L H. The Potential sensitivity of tropical plants to increased Ultraviolet-B radiation. J. Plant Physiol. 1996, 148: 35-41.
Zlotnik I, Dubinsky Z. The effect of light and temperature on DOC excretion by phytoplankton. Limnology and Oceanography, 1989, 34 (6): 831.
陈荷生. 沙坡头地区生物结皮的水文物理特点及其环境意义. 干旱区研究, 1992, 9(1): 31-38.
陈坤, 朱涛, 娄元伟, 饶本强. 紫外线(UV)-B 辐射增强对植物影响的研究进展. 信阳师范学院学报, 2004, 17(3): 359-366.
陈兰周, 刘永定, 李敦海. 盐胁迫对爪哇伪枝藻(Scytonema javanicum)生理生化特性的影响. 中国沙漠, 2003, 23(3): 285-288.
陈兰周, 刘永定, 李敦海, 沈银武, 谢作明. 荒漠藻类及其结皮的研究. 中国科学基金, 2003, 17(2):90-93.
陈兰周, 刘永定, 宋立荣. 微鞘藻胞外多糖在沙漠土壤成土中的作用. 水生生物学报, 2002, 26(2): 155-159.
陈善文, 武宝杆. 藻类对 UV-B 增强的响应及其分子基础. 暨南大学学报, 2000, 21(5): 88-94.
陈拓, 任红旭, 王勋陵. UV-B 辐射对小麦抗氧化系统的影响. 环境科学学报, 1999, 19 (4): 453-455.
陈祝春. 沙丘结皮层形成过程的土壤微生物和土壤酶活性. 环境科学, 1991, 12(1): 19-23.
陈祝春. 不同地带沙丘结皮层的土壤酶活性. 中国沙漠, 1989, 9(1): 85-92.
陈祝春, 李定淑. 固沙植物根际微生物对于沙土发育和流沙固定的影响. 生态学杂志, 1987, 6 (2): 6-12.
崔健宇, 江荣风. 土壤农化分析实验. 北京: 中国农业大学出版社, 1998.
崔燕, 吕贻忠, 李保国. 鄂尔多斯沙地土壤生物结皮的理化性质. 土壤, 2004, 36 (2): 197-202.
段争虎, 刘新民, 屈建军. 沙坡头地区土壤结皮形成机理的研究. 干旱区研究, 1996, 13(2): 31-36.
关桂兰, 杨玉锁, 郭沛新. 新疆干旱地区陆生固氮蓝藻的种群、分布及对环境的作用.干旱区研究,1995,12(1): 1-6.
郭宝江, 庞启深, 阮继红. 螺旋藻多糖对植物细胞辐射遗传损伤的防护效应. 植物学报, 1992, 34: 809-812.
黄泽波. 丝状蓝藻水溶性多糖的研究. 中国科学院水生生物研究所博士论文,1997.
黄泽波, 刘永定. 蓝细菌多糖及其应用研究概况. 生物技术通报, 1997, 4: 26-32.
胡春香. 荒漠藻类及其结皮机理研究. 中国科学院水生生物研究所博士论文, 1999.
胡春香, 刘永定, 宋立荣, 黄泽波. 半荒漠藻结皮中藻类的种类组成和分布. 应用生态学报, 2000a, 11(1): 61-65.
胡春香, 刘永定, 黄泽波, 宋立荣. 荒漠藻壳的精细结构与发育. 水生生物学报, 2000b, 24(1): 11-18.
胡春香, 刘永定, 宋立荣. 土壤藻研究新进展. 水生生物学报, 2002a, 26(5): 521-528.
胡春香, 刘永定, 张德禄等. 荒漠藻结皮的胶结机理. 科学通报, 2002b, 47(12): 931-937.
胡春香, 刘永定. 土壤藻生物量及其在荒漠结皮的影响因子. 生态学报, 2002c, 23(2): 284-292.
胡春香等. 宁夏回族自治区沙坡头地区半荒漠土壤中藻类的垂直分布. 生态学报, 2003, 23(1): 38.
姜海波, 邱保胜. 蓝藻对 UV-B 增强的响应与适应. 西北植物学报, 2005, 25(6): 1259-1268.
贾志军, 王小平. 黄土表面结皮对夏闲坡耕地土壤水分的影响研究. 中国水土保持, 2002, 9: 18-20.
康金花, 关桂兰等. 陆生固氮蓝藻对土壤环境的影响. 干旱区研究, 1998, 15(3): 30-33.
李敦海, 刘永定. 近十年中国地木耳研究概况. 水生生物学报, 2003, 27(4): 408-412.
李敦海. 拟球状念珠藻(葛仙米)形态建成与发育及其生理学研究. 中国科学院水生生物研究所博士论文, 2000a.
李敦海, 宋立荣, 刘永定. 念珠藻葛仙米叶绿素荧光与水分胁迫的关系. 植物生理学通讯, 2000b, 36(3): 205-208.
李敦海, 宋立荣, 刘永定. 念珠藻葛仙米的藻殖段分化——信号转导参与过程的初步研究. 植物学通报, 2002, 19(3): 328-335.
李合生等. 植物生理生化实验原理和技术. 北京, 高等教育出版社, 2000.
凌裕泉, 屈建军, 胡玫. 沙面结皮形成与微环境变化.应用生态学报, 1993, 4(4): 393-398.
李守中, 肖洪浪等. 腾格里沙漠人工固沙植被区生物土壤结皮对降水的拦截作用. 中国沙漠, 2002, 22: 612-616.
刘永定, 黎尚豪. 长江中游黄棕壤地区几种稻田土壤的蓝藻种类及田间季节差异与垂直分布. 见: 廉正编. 长江流域资源、生态、环境与经济开发研究论文集. 1988, 北京: 科学出版社, 266-269.
刘永定, 黎尚豪. 土壤藻类及其生理生态. 水生生物学报, 1993, 17(3): 272-277.
刘永定, 沈银武, 宋立荣等. 黄河中游土壤类的种类组成与土壤肥力的关系. 水生生物学报, 1999, 23(5): 434-442.
李新荣, 贾玉奎, 龙利群等. 干旱半干旱地区土壤微生物结皮的生态学意义及若干研究进展. 中国沙漠, 2001, 21(1): 4-12.
李新荣, 张景光, 王新平等. 干旱沙漠区土壤微生物结皮及其对固沙植被影响的研究. 植物学报, 2000, 42(9): 965-970.
李运广, 高坤山. 盐胁迫对地木耳和葛仙米生理生化特性的影响. 水生生物学报, 2003, 27(3): 227-231.
吕贻忠, 杨佩国. 荒漠结皮对土壤水分状况的影响. 干旱区资源与环境, 2004, 18(2): 76-79.
贾宝全, 张红旗, 张志强, 慈龙骏. 甘肃省民勤沙区土壤结皮理化性质研究. 生态学报, 2003, 23(7): 1442-1448.
马红樱, 张德禄, 胡春香等. 植物活性多糖的研究进展. 西北师范大学学报(自然科学版), 2004, 40(3): 112-117.
缪锦来, 阚光锋, 李光友等. UV-B 辐照培养下南极冰藻的形态和超微结构及主要生化组成的变化. 中国海洋药物, 2003, 6: 1-5.
牛玉璐, 曹永胜. 生物结皮及其在荒漠治理中的作用. 生物学教学, 2005, 30(10): 5-6.
庞启深, 郭宝江, 阮继红. 螺旋藻多糖对核酸内切酶活性和 DNA 修复合成的增强作用. 遗传学报, 1988, 5: 374-381.
庞启深, 郭宝江, 阮继红. 螺旋藻抗辐射多糖的提纯和分析. 生物化学与生物物理学报, 1989, 21: 445-449.
尚玉昌. 普通生态学. 北京, 北京大学出版社, 2002.
王爱国, 邵从本, 罗广华. 丙二醛作为植物脂质过氧化指标的探讨. 植物生理学通讯, 1986, 2: 55-57.
王静. 地木耳改变土壤含氮肥量的研究. 兰州大学学报(自然科学版), 1995, 31( 3): 97-99.
魏培莲. 微生物胞外多糖研究进展. 浙江科技学院学报, 2002, 14(2): 8-12.
吴发启, 范文波. 坡耕地黄墡土结皮的理化性质分析. 水土保持通报, 2001, 21(4): 22-24.
吴楠, 潘伯荣, 张元明等. 古尔班通古特沙漠生物结皮中土壤微生物垂直分布特征. 应用与环境生物学报, 2005, 11 (3): 349～353.
吴楠, 潘伯荣, 张元明. 土壤微生物在生物结皮形成中的作用及生态学意义. 干旱区研究, 2004, 21(4): 444-450.
吴玉环, 高谦, 于兴华. 生物土壤结皮的分布影响因子及其监测. 生态学杂志, 2003, 22(3): 38-42.
杨晓辉, 张克斌, 赵石杰. 生物土壤结皮——荒漠化地区土壤研究的热点问题. 生态学报, 2001, 21(3): 474-480.
尤珊, 郑必胜, 郭祀远. 氮源对螺旋藻生长及胞外多糖的影响. 食品科学, 2004, 25(4): 32-35.
尤珊, 郑必胜, 郭祀远. 光照对螺旋藻形态及胞外多糖的影响和机理. 海湖盐与化工, 2004, 33(1): 23-25.
张丙昌, 张元明, 赵建成. 古尔班通古特沙漠生物结皮藻类的组成和生态分布研究. 西北植物学报, 2005, 25 (10): 2048-2055.
张大伟, 王艳, 蔡伟民. 沙尘暴源头控制的新思路. 上海环境科学, 2003, 增刊: 1-4.
张殿忠, 汪沛洪, 赵会贤. 测定小麦叶片游离脯氨酸含量的方法. 植物生理学通讯, 1990, 4: 62-65.
张光远, 蔡崇法. 黄绵土结皮的微形态特征及某此理化性质的研究. 见:中国—加拿大. 晋西黄土高原土壤侵蚀规律实验研究文集. 北京:水利电力出版社. 1990, 58-67.
张景钺, 梁家骥. 植物系统学. 北京: 人民教育出版社, 1978.
张继贤, 邸醒民, 王淑湘等. 沙坡头地区防护林体系建立过程中生态环境变化的特点. 干旱区资源与环境, 1994, 8(3): 68-79.
张利平. 天然吸附剂——壳聚糖的最新研究. 阴山学刊, 2001, 5: 42-44.
张维杰. 复合多糖生化研究技术. 上海: 上海科学技术出版社, 1987.
张元明, 曹同, 潘伯荣. 干旱与半干旱地区苔藓植物生态学研究综述. 生态学报, 2002, 22(7): 1129-1134.
赵吉, 邵土琴. 库布齐沙地土壤的生物学活性研究. 内蒙古大学学报(自然科学版), 1997, 28(5): 664-666.
赵玲, 尹平河等. 海洋赤潮生物原甲藻对重金属的富集机理. 环境科学, 2001, 22(4): 42-45.
郑有飞等. 紫外辐射增强对大豆影响的进一步分析. 环境科学学报, 1998, 18(5): 549-552.
钟泽璞, 施定基. 丝状体蓝藻藻殖段的分化及其调节机制. 植物学通报, 2000, 17(3): 204-210.
周礼恺. 土壤酶学. 北京: 科学出版社, 1987.
周志刚, 程子俊, 刘志礼. 沙漠结皮中藻类生态的研究. 生态学报, 1995, 15(4): 385-391.
周志刚, 刘志礼, 刘雪娴. 极大螺旋藻多糖的分离、纯化及其抗氧化特性的研究. 植物学报, 1997, 39: 77-81.
祝建, 王俊, 华振基等. 高压冷冻和低温替代技术制备的发菜营养细胞的超微结构. 植物学报, 1998, 40(10): 901-905.
Aguirre-von Wobeser E, Figueroa F L, Cabello-Pasini A. Effects of UV radiation on photoinhibition of marine macrophytes in culture systems. Appl. Phycol. 2000, 12: 159–168.
Ana O, Massimo V. Extracellular polysaccharide synthesis by Nostoc strains as affected by N source and light intensity. Journal of Biotechnology, 2003, 102: 143-152.
Andreas H, Cornelius L. Algae and UV irradiation: Effects on ultrastructure and related metabolic functions. Micron, 2006, 37: 190-207.
Angela H S, Dominic A H, Brendan J K. A critical assessment of the analysis and distributions of scytonemin and related UV screening pigments in sediments. Organic Geochemistry, 2004, 35: 1221-1228.
Angelova M, Petricheva E. Glucose- and nitrogen-dependence of acid proteinase production in semicontinuous culture with immobilized cells of Humicola lutea 120-5. Journal of Biotechnology, 1997, 58: 51–58
Araoz R, Háder D P. Ultraviolet radiation induces both degradation and synthesis of phycobilisomes in Nostoc sp. a spectroscopic and biochemical approach. FEMS Microbiol. Ecol., 1997, 23: 301-313.
Araoz R, Lebert M, Háder D P. Translation activity under ultraviolet radiation and temperature stress in the cyanobacterium Nostoc sp. J. Photochem. Photobiol. B Biol., 1998a, 47: 115-120.
Araoz R, Shelton M, Lebert M, et al. Differential behavior of two cyanobacteria species to UV radiation. Artificial UV radiation induces phycoerythrin synthesis. J. Photochem. Photobiol. B Biol., 1998b, 47: 175-183.
Arnotts T, Murphy T M. A comparison of the effects of a fungal elicitor and ultraviolet radiation on ion transport and hydrogen peroxide synthesis in rose cells. Environ Exp Bot, 1991, 31: 209-216.
Asthana R K, Chatterjee S, Singh S P. Investigations on nickel biosorption and its remobilization. Process Biochem, 1995, 30: 729–34.
Bailey D, Andrew P M, James R R. Aggregation of soil particles by algae. J. Phycol, 1973, 9, 99-101.
Baily D, Mazurak A P, Rosowski J R. Aggregation of soil particles by algae. Journal of Phycology, 1973, 9: 99-101.
Band C J, Arredondo-Vega B O, Vazquez-Duhalt R, et al. Effect of salt-osmotic upshock on the edaphic microalga Neochlaris oleoabundans. Plant Cell and Environment, 1992, 15: 129-133.
Banerjee M, Hader D P. Effects of UV radiation on the rice field cyanobacterium, Aulosira Fertilissima. Environmental Experimental Botany. 1996, 36(3): 281-291.)
Barbara N, Adriana P, Licia L, et al. Chemical composition and production of exopolysaccharides from representative members of heterocystous and non-heterocystous cyanobacteria. Phytochemistry, 1999, 52: 639-647.
Bell R A. Cryptoendolithic algae of hot semiarid lands and deserts. Journal of Phycology, 1993, 29: 133-139.
Belnap, Harper K T, Warren S D. Surface disturbance of cryptobiootic soil crusts: nitrogennase activity, chlorophyll content and chlorophyll degradation. Arid Soil Research and Rehabilitation, 1994, 8: 1-8.
Belnap J, Gardner J S. Soil microstructure in soils of the Colorado Plateau: the role of the cyanobadterium Microcoleus vaginatus. Great Basin Nat, 1993, 53: 40-47.
Belnap J, Gilletc D A. Vulnerability of desert biological soil crust to wind erosion: the influences of crust development, soil textuts and disturbance. Journal of Arid Environment, 1998, 39: 133-142.
Bennet A, Bogorad L. Complementary chromatic adaptation in a filamentous blue-green alga. J Cell Biol., 1973, 58: 419-435.
Biagini A B, Kirk K, Schofield P J, et al. Role of K+ and amino acids in osmoregulation by the free-living microaerophilic protozoon Hexamita inflata. Microbiol., 2000, 146: 427- 433.
Bilger W, Budel B. Photosynthetic activity of two developmental stages of a Nostoc strain (cyanobacteria) isolated from Ceosiphon pyriforne (Mycota). Phycol, 1994, 30: 225-230
Bloor S, England R R. Antibiotic production by the cyanobacterium Nostoc muscorum. J. Appl. Phyco., 1989, 1: 367-372.
Bold H C, Wynoc M J. Introduction to the Algae. PRENTICE-HALL, INC., London, 1978, 37-39.
Bongale U D. Distribution of Nostoc and Anabaena (Cyanophyta) in relation to soil propertiel in the cultivated soils of Karnataka state (India). Cryptogamie/Algologie, 1987, 8 (1): 13-18.
Booth W E. Algae as pioneers in plant succession and their importance in erosion control. Journal of Phycology, 1941, 11: 316-320.
Bothwell M L, Sherbot D, Pollock C M. Ecosystem response to solar ultraviolet-B radiation: Influence of trophic-level interactions. Science, 1994, 265: 97-100.
Bowler C, Montagu M V, Inze D. Superoxide dismutase and stress tolerance. Ann Rev Plant Physiol Plant Mol Biol., 1992, 43: 83-116.
Bradford M. A rapid and sensitive method for the quantification of microgram quantities of protein utilizing the principle of protein-dye binding. Anal. Biochem., 1976, 72: 248-254.
Bredt D S, Hwang P M, Glatt C E, et al. Cloned and expressed nitric oxide synthase structurally resembles cytochrome P-450 reductase. Nature, 1991, 351: 714-771.
Brenowitz S, Castenhol Z R W. Long-term effects of UV and visible irradiance on natural population of a scytonemin-containing cyanobacterium (Calothirix sp.). FEMS Microbiol Ecol., 1997, 24: 343-352.
Britt A B. Repair of DNA damage induced by ultraviolet radiation. Plant Physiol., 1995, 108: 891-896.
Broady P A. Taxonomic and ecological investigations of algae on steam-warmed soil on Mt Erebus Ross Island, Antarctica. Phycologia, 1984, 23(3): 257-271.
Caiola M G, Daniela B, Friedmann E I. Effect of desiccation on envelopes of the cyanobacterium Chrococcidicpsis sp. (Chroococcales). Eur. J. Phycol, 1996, 31: 97-105.
Caire G Z, Cano M S, Mulé M C Z, et al. Action of cell-free extracts and extracellular products of Notoc muscorum on growth of Sclerotinia sclerotiorum. Phyton, 1987, 47: 43-36.
Caire G Z, Cano M S, Mulé M C Z, Halperin D R. Antimycotic products from the cyanobacterium Nostoc muscorum against Rhizoctonia solani. Phyton, 1990, 51: 1-4.
Campbell D, Eriksson S M J, Oquist G, et al. The cyanobacterium Synechococcus resists UV-B by exchanging photosystem Ⅱ reaction-center D1 proteins. Proc. Natl. Acad. Sci. USA, 1998, 95: 364-369.
Campbell S E. Soil stabilization by a prokaryotic desert crust: implications for precambrian land biota. Origins of life, 1979, 9: 335-348.
Castenholz R W. Multiple strategies for UV tolerance in cyanobacteria. Spectrum, 1997, 10: 10-16.
Castenholz R W, Garcia-Pichel F. Cyanobacterial responses to UV radiation. Whitton B A, Pottsm, eds. The ecology of cyanobacteria: their diversity in time and space. Kluwer Academic Publishers, 2000: 591-611.
Castenholz R W, Waterbury J B. Cyanobacteria. In: Bergey’s Manual of Systematic
Bacteriology (Staley, J.T., Bryant, M.P., Pfenning, N. and Holt, J.G., Eds.), 1989, Vol. 3, pp. 1710-1799. Williams and Wilkins, Baltimore, MD.
Chen L Z, Li D H, Liu Y D. Salt tolerance of Microcoleus vaginatus Gom., a cyanobacterium isolated from desert algal crust, was enhanced by exogenous carbohydrates. Journal of Arid Environments, 2003, 55: 645–656.
Chu H J, Tsang C T. Research and utilization of cyanobacteria in China: a report. Arch. Hydrobiol. Suppl. 1988, 80: 1-4.
Cockell C S, Knowland J. Ultraviolet radiation screening compounds. Biol. Rev., 1999, 74: 311-345.
Conde F R, Churiom S, Previtali C M. The photoprotector mechanism of mycosporine-like amino acids. Excited-state properties and photostability of porphyra-334 in aqueous solution. J. Photochem. Photobiol. B Biol., 2000, 56: 139-144.
Correia C M, Arealelv, Torres-Pereira M S, et al. Intraspecific variation in sensitivity to ultraviolet-B radiation in maize grown under field conditions. I. growth and morphological aspects. Field Crops Research, 1998, 59: 81-89.
Costerton J W, Irvin R T, Cheng K J. The bacterial glycocalyx in nature and disease. Annu.Rev. Microbiol, 1981, 35: 299-324.
Crutzen P J. Ultraviolet on the increase. Nature, 1992, 356: 104-105. Davey M C, Clarke K J. Fine structure of a terrestrial cyanobacterial mat from Antarctica. J Phycol, 1992, 28: 199-202.
Dillon J G, Tatsumicm, Tandingan P G, et al. Effect of environmental factors on the synthesis of scytonemin a UV-screening pigment, in a cyanobaterium (Chroococcidiopsis sp.). Arch. Microbiol., 2002, 177: 322-331.
Doanhue B A, Taylor J S, Reinesd. Transcript cleavage by RNA Polymerase (2) arrested by acyclobutane dimmer in the DNA template. Proc. Natl. Acad. Sci. USA., 1994, 91: 8502-8506.
Doers M, Parker D L. Properties of Microcystis aeruginosa and M. flos-aquae (Cyanophyta) in culture. J Phycol, 1988, 24: 502–8.
Dohler G, Hagmeier E, David C H. Effect of solar and artificial UV irradiation on pigments and assimilation of 15N ammonium 15N nitrate by macroalgae. J. Photochem. Photobiol. B Biol., 1995, 30: 179-187.
Domenico V, Herlinda G V, Gabriel C. Nitrogen removal and recycling by Scenedesmus obliquus in semicontinuous cultures using artificial wastewater and a simulated light and temperature cycle. Bioresource Technology, 2005, 96: 359-362.
Donkor V, Káder D P. Effects of solar and ultraviolet radiation on motility, photomovement and pigmentation in filamentous, gliding cyanobacteria. FEMS Microbiol. Ecol., 1991, 86: 159-168.
Durrell L W, Shields L W. Characteristics of soil algae relation to crust formation. Trans. Am.Microbiol. Soc, 1961, 80(1): 73-79.
Eldridge D T, Greene R S B. Microbiotic soil crusts: a review of their roles in soil and ecological processes in the rangelands of Australia. Australian Journal of Soil Research, 1994a, 32: 389-415.
Eldridge D T, Greene R S B. The effect of time since fire on the cover and composition of cryptogamic soil crusts on an Encalypus shrubland soil. Cunninghamia, 1994b, 3: 581-599.
Enlings M. UV-B induced synthesis of photoprotective pigments and extracellular polysaccharides in terrestrial cyanobaterium Nostoc commune. Bacteriol, 1997, 179(6): 1940.
Farman J C, Gard N B G, Shan K J D. Large losses of total ozone in Antarctica reveal seasonal CLOx/NOx. Nature, 1985, 315: 207-210.
Farooq M, Suresh B G, Ray R S, Misra R B, Shanker U, Hans R K. Sensitivity of duckweed (Lemna major) to ultraviolet-B radiation. Biochem. Biophys. Res. Commun. 2000, 276: 970–973.
Farooq M, Shankar U, Ray R S, Misra R B, Agrawal N, Verma K, Hans R K. Morphological and metabolic alterations in duckweed (Spirodela polyrhiza) on long-term low-level chronic UV-B exposure. Ecotoxicology and Environmental Safety, 2005, 62: 408-414.
Fauchot J, Gosselin M. Influence of UV-B radiation on nitrogen utilization by a natural assemblage of phytoplankton. J. Phycol., 2000, 36: 484-496.
Ferran G P, Richard W, Castenholz. Characterization and biological implications of scytonemin, a cyanobacteria sheath pigment. J. Phycol., 1991, 27: 395-409.
Foyer C. Photosynthesis. New York: John Wiley and Sons Inc, 1984, 60-70.
Frantz G. Polysaccharides in pharmacy: current applications and future concepts. Planta Med, 1989, 55: 493–7.
Friedmann E I, Hua M, Ocampo-Friedmann J A. Crpytoendolithic lichen and cyanobacterial microbial community of the Ross Desert. Polarforschung, 1988, 58: 251-259.
Friedmann E I, Ocampo-Friedmann R. A primitive cyanobacterium as pioneer microorganism for terraforming Mars. Adv. Space Res, 1995, 15(3): 243-246.
Frisog, Speteac, Giacomettigm. Degradation of photosystem Ⅱ reaction center D1 polypeptide induced by UV-B radiation in isolated thylakoids. Identification and characterization of C- and N-terminal breakdown products. Biochim. Biophys. Acta, 1994, 1184: 78- 84.
Gadd G M. Heavy metal accumulation by bacteria and other microorganisms. Experientia, 1990, 46: 834–42.
Garcia-Pichel F, Belnap J. Microenvironments and microscale productivity of cyanobacterial desert crusts. J. Phycol, 1996, 32: 774–782.
Gerhardt K E, Wilson M I, Greenberg B M. Ultraviolet wavelength dependence of photomorphological and photosynthetic responses in Brassica napus and Arabidopsis thaliana. Photochem. Photobiol. 2004.
Giannopotitis C N, Ries S K. Superoxide dismutase in higher plants. Plant Physiology, 1977, 59: 309-314.
Gotz T, Whidhovel U, Boger P, et al. Protection of photosynthesis against ultraviolet-B radiation by carotenoids in transformants of the cyanobacterium Synechococcus PCC 7942. Plant Physiol., 1999, 120: 599-604.
Gourr K, Pandey P K, Bisen P S. Differential response in damage and repair of wild-type Anacystis nidulans and its UV-B plus heat shock tolerant (UV-HSt) strain under UV-B and heat shock stress. J. Photochem. Photobiol. B Biol., 1997, 40: 61- 67.
Greene R S B, Chanres C J. The effect of fire on the soil and the degraded semiarid woodland. Cryptogam cover and physiea microphological properties. Australian J soil Res., 1990, 755-777.
Gromov B V, Vepritskiy A A, Titova N N, et al. Production of the antibiotic cyanobacterin LU-1 by Nostoc linckia CALU 892 (cyanobacterium). J. Appl. Phycol. 1991, 3: 55-59.
Gupta V V S R, Germida J J. Distribution of microbial biomass and its activity in soil aggregate size classes as affected by cultivation. Soil Biol Biochem, 1988, 20: 777-786.
Güven K C, Ozsoy Y, Ulutin O N. Anticoagulant, fibrinolytic and antiaggregant activity of carrageenans and alginic acid. Bot Mar, 1991, 34: 429–432.
Hall D O, Rao K K. Photosynthesis (Fourth Edition), Edward Arnold, London, 1987: 18-23.
Harper K T, Marble J R. A role for nonvascular plants in management of arid and semiarid rangeland. In: Tueller P T. (ed).Vegetation Science Applications for Rangeland Analysis and Management. Dordrecht: Kluwer Academic Publisher, 1988, 135-169.
Hellebust J A. Mechanisms of response to salinity in halotolerant microalgae.Plant and Soil, 1985, 89: 69-81.
Hernando M P, Ferreyra G A. The effects of UV radiation on photosynthesis in an Antarctic diatom (Thalassiosira sp.): Does vertical mixing matter? Journal of Experimental Marine Biology and Ecology, 2005, 325: 35-45.
He Y Y, Háder D P. Involvement of reactive oxygen species in the UV-B damage to the cyanobacterium Anabaena sp.. J. Photochem. Photobiol. B Boil., 2002a, 66: 73-80.
He Y Y, Háder D P. UV-B-induced formation of reactive oxygen species and oxidative damage of the cyanobacterium Anabaena sp.: protective effects of ascorbic acid and N-acetyl-L-cysteine. J. Photochem. Photobiol. B Boil., 2002b, 66: 115-124.
Hidege, Vassi. UV-B induced free radical production in plant leaves and isolated thoylakoid membranes. Plant Sci., 1996, 115: 251-260.
Hill D R, Keenan T W, Helm R F, et al. Extracellular polysaccharide of Nostoc commune (cyanobacteria) inhibits fusion of membrane vesicles during desiccation. J. Applied. Phycol., 1997, 9: 237-248.
Holm-Hansen O, Helbling G W, Lubin D. Ultraviolet radiation in Antarctica: inhibition of primary production. Photochem. Photobiol, 1993, 58: 567– 570.
Hoppe H A. Marine algae and their products and constituents in pharmacy. In Hoppe, H.A, Levring & T. Tanaka, Y. [Eds.] Marine Algae in pharmaceutical Science. Walter de Gruyter, Berlin, 1979, 1: 25-119.
Hori K, Ishibashi G, Okita T. Hypocholesterolemic effect of blue-green alga ishikurage (Nostoc commune) in rats fed atherogenic diet. Plant Foods Hum. Nutr, 1994, 45: 63～70.
Hpknal, Bondma, Tobnak. Effects of UV-B on the development and ultrastructure of the primary leaf of wheat (Triticum aestivum). J. Exp. Bot., 1996, 47(sup): 20.
Huang Z B, Liu Y D, et al. Studies on polysaccharides from three edible species of Nostoc (cyanobacteria) with different colony morphologies: comparison of monosaccharide compositions and viscosities of polysaccharides from field colonies and suspension cultures. J. Phycol, 1998, 34: 962–968.
Hu C X, Liu Y D, Song L R, Zhang D L. Effect of desert soil algae on the stabilization of fine sands. Journal of Applied Phycology, 2002a, 14: 281-292.
Hu C X, Liu Y D, Zhang D L, Huang Z B, Paulsen B S. Cementing mechanism of algal crusts from desert area. Chin Sci Bull, 2002b, 47: 1361-1368
Hu C X, Liu Y D, et al. Extracellular carbohydrate polymers from five desert soil algae with different cohesion in the stabilization of fine sand grain. Carbohydrate Polymers, 2003a, 54: 33-42.
Hu C X, Liu Y D. Primary succession of algae community structure in desert soil. Acta Botanica Sinica, 2003, 45 (8): 917-924.
Hu C X, Zhang D L, Huang Z B, Liu Y D. The vertical microdistribution of cyanobacteria and green algae within desert crusts and the development of the algal crusts. Plant and Soil, 2003c, 257: 97-111.
Huheihel M, Ishanu V, Tal J, Arad A. Activity of Porphyridium sp. polysaccharides against Herpex simplex viruses in vitro and in vivo. J. Biochem. Biophys. Methods, 2001, 50: 189-200.
Itoh H, Noda H, Amano H, Zhuaug C, Mizuno T, Ito H. Antitumor activity and immunological properties of marine algal polysaccharides, specially fucoidan, prepared from Sargassum thunbergii of Phaeophyceae. Anticancer Res., 1993, 13: 2045-2052.
Jansen M A K, Noort V D, Tan M Y, et al. Phenol-oxidizing peroxidases contribute to the protection of plant from ultraviolet radiation stress. Plant Physiol, 2001, 126: 1012-1023.
Janssen L H J, Hasselt. Temperature-induced alterations of in vivo chlorophyll a fluorescence in cucumber as affected by DCMU. Photosynth Res., 1988, 15: 153-162.
Jarman T R, Deavin L, Slocombe S, Rhighelato R C. Investigation of the effect of environmental conditions on the rate of exopolysaccharide synthesis in Azotobacter vinelandii. J. Gen. Microbiol., 1978, 107: 59–64.
Johansen J R. Cryptogamic crusts of semiarid and arid lands of North America. J Phycol, 1993, 29: 140.
Johnston H S. Reduction of stratospheric ozone by nitrogen oxide catalysts from supersonic transport exhaust. Science, 1971, 173: 517-522.
Jordan B R, James P E, Mackerness S A H. Factors affecting UV-B induced changes in arabiodopsis thaiana L. gene expression: the role of development protective pigments and the chloroplast signal. Plant Cell Physiol, 1998, 39 (7): 769-778.
José M, ángeles V, et al. Exopolysaccharide production by the cyanobacterium Anabaena sp. ATCC 33047 in batch and continuous culture. Journal of Biotechnology, 1998, 60: 175-182
José M, ángeles V, et al. Outdoor cultivation of a nitrogen-fixing marine cyanobacterium, Anabaena sp. ATCC 33047. Biomolecular Engineering, 2003, 20: 191-197.
Kaplan D, Christiaen D, Arad S M. Binding of heavy metals by algal polysaccharides. In Stadler T, Mallion J, Verdus M C, Karamanos Y, Morvan H, Christiaen D. (Eds.) Algal Biotechnology. Elaevier Applied Science, London and New York, 1988, 179-187.
Karentz D, Ceaver J E, Mitchell D L. DNA damage in the Antarctic. Nature, 1991, 350: 28.
Karentz D, et al. Impact of UV-B radiation on pelagic freshwater ecosystems: Report of working group on bacteria and phytoplankton. Arch. Hydrobiol, 1994, 43: 31-69.
Kennedy J F, White C A. Bioactive Carbohydrates in Chemistry, Biochemistry and Biology. Ellis Horwood Ltd., Chichester, England, 1983.
Kidron G J, Barzilay E, Sachs E. Microclimate control upon sand microbiotic crust, western Negev Desert, Israel. Geomorphology, 2000, 36: 1-18.
Kollib, Tiwaris, Mohantyp. Ultraviolet-B induced damage to photosystem Ⅱ in intact filaments of Spirulina platensis. Nature, 1998, 53: 369- 377.
Kramer G F, Norman H A, Krizek, et al. Influence of UV-B radiation on polyamines, lipid peroxidation and membrane lipids in cucumber. Phytochemistry, 1991, 30 (7): 2101-2108.
Krause G H, Weis E. Chlorophyll fluorescence as a toll in plant physiology. Ⅱ. Interpretation of fluorescence signals. Photosybthesis Res., 1984, 5: 139-157.
Kumar A, Sinha R P, Háder D P. Effect of UV-B on enzymes of nitrogen metabolism in the radiation in the cyanobacterium Nostoc calcicola. J. Plant Physiol., 1996, 148: 86-91.
Kumar A, Tyagim B, Jhapn, et al. Inactivation of cyanobacterial nitrogenase after exposure to ultraviolet-B radiation. Curr. Microbiol., 2003, 46: 380-384.
Lange O L, Meyer A, Zellner H. Photosynthesis and water relation of lichen soil crusts: field measurements in the coastal fog zone of the Namib Desert. Functional Ecology, 1994, 8: 253-264.
Lao K Q, Alexander N G. Ultraviolet-B photodestruction of a light-harvesting complex. Proc. Natl. Acad. Sci. USA., 1996, 93: 5258-5263.
Leavitt P R. A review of factors that regulate carotenoid and chlorophyll deposition and fossil pigment abundance. J. Paleolimnol. 1993, 9: 109-127.
Leys J F. Coverlevels to control soil and nutrient loss from wind erosion on sand plain country in central N.S.W.Proc. 7th Biennial Conference of the Aust. Rangel. Soc. Cobar, 1992, 84-91.
Leys J F. Soil crusts, their effect on wind erosion. Soil Conservation service of N.S.W. Research Note, 1990.
Li X R, Zhang J G, Wang X P, et al. Study on soil microbiotic crust and its influences on sand-fixing vegetation in arid desert region. Acta Botanica Sinica, 2002, 42(9): 965- 970.
Liu H, Buskey E J. Hyper salinity enhances the production of extracellular polymeric substance (EPS) in the texas brown tide alga, Aureoumbra Lagunensis (Pelagophyceae) . J. Phycol., 2000, 36: 71-77.
Liu Y D & Li S H. Species composition and vertical distribution of blue-green algae in rice field soil, Hubei, China. Nova Hedwigia, 1989, 48: 55-67.
Liu Y D, Shen Y W, Song L R, et al. Species composition and distribution of blue-green algae from soil in the middle reach of Yellow River, China. Proceeding of international conference on Asian Network on microbial researches, 1998, 395-401.
Lukesova A. Soil algae in four secondary successional stages on abandoned fields. Algological Studies, 1993, 71: 81-102.
Lynch J M, Bragg E. Microorganisms and soil aggregate stability. Advances in Soil Science, 1985, 2: 133-171.
Lynch J M. Interactions between biological processes, cultivation and soil structure. Plant Soil, 1984, 76: 307-318.
Mackerness A H, John C F, Jordan B, et al. Early signaling components in ultraviolet-B responses: distinct roles for different reactive oxygen species and nitric oxide. FEBS lett, 2001, 489 (2): 237-242
Mackerness A H, Jordon B R, Thoma S B. Reactive oxygen species in the regulation of photosynthetic genes by ultraviolet-B radiation in green and etiolated buds of pea (Pisum sativum L.). J. Photochem. Photobiol. B Boil., 1999, 48: 180-188.
Mackerness A H. The effect of supplemental ultraviolet-B radiation on mRNA transcripts, translation and stability of chloroplast proteins and pigment formation in Pisum sativum L. J. Exp Bot, 1997, 48: 729-738.
Malanga G, Puntarulo S. Oxidative stress and antioxidant content in Chlorellavulgaris after exposure to ultraviolet-B radiation. J Physiologia Plantarum, 1995, 94: 672-679.
Mata L, Silva J, Schuenhoff A, Santos R. The effects of light and temperature on the photosynthesis of the Asparagopsis armata tetrasporophyte (Falkenbergia rufolanosa), cultivated in tanks. Aquaculture, 2006, 252: 12-19.
MáTé Z, Sass L, Szekeresm, et al. UV-B induced differential transcription of psbA genes encoding the D1 protein of photosystem Ⅱ in the cyanobacterium Synechocystis 6803. J. Biol. Chem., 1998, 273: 17439-17444.
Mazor G, Kidron G J, Vonshak A, Abeliovich A. The role of cyanobacterial exopolysaccharides in structuring desert microbial crusts. FEMS Microbiology Ecology, 1996, 21: 121-130.
Mehta V B & Vaidya B S. Cellular and extracelluar polysaccharides of the blue-green alga Nostoc. J. Exp. Bot. 1978,29: 1423-1430.
Metting B. The systematic and ecology of soil algae. The Bot. Rev., 1981, 47(2): 195-312.
Monika E S, Wolfgang B, Ssiegfried S. UV-B-induced synthesis of photoprotective pigments and extracellular polysaccharides in the terrestrial cyanobacterium Nostoc commune. J. Bac. Mar., 1997, 179: 1940-1945.
Murphy T M. Effect of broad-band ultraviolet and visble radiation in hydrogen peroxide formation by cultured rose cells. Physiol. plant, 1990, 80: 63-78.
N?geli C. Gattungen einzelliger Algen, physiologisch and systematisch bearbeitet, Neue Denkschrift, Allg. Schweiz. Natur Ges. 1849, 10: 1-138.
Noctor G, Foyer C H. Ascorbate and glutathione: Keeping active oxygen under control. Annual Review of Plant Physiology and Plant Molecular Biology, 1998, 49: 249-279.
Pang Q S, Guo B J & Ada K. Radioprotective effect of extract from Spirulina platensis in mouse bone marrow cells studied by using the micronucleus text. Toxico. Let., 1989,48: 165-169.
Patterson G. Antiviral activity of cultured blue-green algae (Cyanophyta). J. Phycol. 1993, 29: 125~130.
Peter R L, Rolf D V, David B D, John P S, David W S. Past ultraviolet radiation environments in lakes derived from fossil pigments. Nature, 1997, 388: 457- 459.
Peterson J B. Studies on the biology and taxonomy of soil algae. Dansk Botanisk Arkiv, 1935, 8(9): 8-70.
Pintome, Casatip, Hsutp, et al. Effects of UV-B radiation on growth, photosynthesis, UV-B-absorbing compounds and NADP-malic enzyme in bean (Phaseolus vulgaris L.) grown under different nitrogen conditions. J. Photochem. Photobiol. B Biol., 1999, 48: 200-209.
Portwich A, Garcia P F. Ultraviolet and osmotic stresses induce and regulate the synthesis of mycosporines in the cyanobacterium Chlorogloeopsis PCC 6912. Arch. Microbiol., 1999, 172: 187-192.
Potts M. Chroococcus S24 and Chroococcus N41(cyanobacteria): morphological, biochemical and genetic characterization and effects of water stress on ultrastructure. Arch Microbiol, 1983,135: 81-90.
Potts M. Minireview: Mechanisms of desiccation tolerance in cyamobacteria. Eur. J. Phycol., 34: 319-328.
Prabha G L, Kulandaivelu G. Induced UV-B resistance against photosynthesis damage by adaptive mutagenesis in Synechococcus PCC 7924. Plant Sci., 2002, 162: 663-669.
Preusss B, Britta B. A DNA-damage-induced cell cycle checkpoint in Arabidopsis. Genetics, 2003, 164: 323- 334.
Prosperi C. Environmental factors affecting in vitro nitrogenase activity of cyanobacteria isolated from rice-fields. J. Applied. Phycol, 1992, 4: 197-204.
Proteau P J, Gerwick W H, Garcia P, Castenholz R W. The structure of scytonemin, an ultraviolet sunscreen pigment from the sheaths of cyanobacteria. Experientia, 1993, 49: 825-829.
Quaite F E. DNA damage levels setermine cyclobutyl pyrimidine dimer repair mechanisms in alfalfa seedings. Plant Cell, 1994, 6: 1635-1641.
Quaite F E, Sueherland B M, Sutherland J C. Action spectrum for DNA damage in alfalfa lowers predicted impact of ozone depletion. Nature, 1992, 358: 576- 578.
Rail C. Interactive effects of UV-B and copper on photosynthetic activity of the cyanobacterium Anabaena doliolum. Environ Exp Bot, 1995, 35(2): 177.
Rajapopal S, Murthysd D, Mohanty P. Effect of ultraviolet-B radiation on intact cells of the cyanobacterium Spirulina platensis characterization of the alteration in the thylakiod membranes. J. Photochem. Photobiol. B Boil., 2000, 54: 61- 66. Rao AV, Venkatesward. Microbial ecology of the soil of Indian Desert. Agri Ecosyst & Environ, 1983, 10(4): 498～513.
Rao M V, Palivath G, Ormrod D P. Ultraviolet-B and ozone-induced biochemical changes in antioxidant enzymes of A rabidopsis thaliana. Plant Physiol, 1996, 110: 125-136.
Reddy K J, Soper B W, Tang J, Bradley R L. Phenotypic variation in exopolysaccharide production in the marine, aerobic nitrogen-cxing unicellular cyanobacterium Cyanothece sp. World J. Microbiol. Biotechnol. 1996,12: 311-318.
Rippka R, Deruelles J W J B, Herdman M, Stanier R Y. Generic assignments, strain histories and properties of pure cultures of cyanobacteria. J Gen Microbiol, 1979, 111: 1-61.
Roberto D P, Massimo V. Outermost polysaccharidic investments of cyanobacteria: Nature, significance and possible applications. Recent Res. Devel. Microbiology, 2003b, 7: 13-22.
Roberto D P, Raffaella P, et al. Assessment of the metal removal capability of two capsulated cyanobacteria, Cyanospira capsulata and Nostoc PCC7936. Journal of Applied Phycology, 2003a, 15: 155-161.
Roberto D P, Vincenzini M. Exocellular polysaccharides from cyanobacteria and their possible applications. FEMS Microbiol Rev, 1998, 22: 151–75.
Rómulo A, H?der D P. Ultraviolet radiation induces both degradation and synthesis of phycobilisomes in Nostoc sp.: a spectroscopic and biochemical approach. FEMS Microbiology Ecology, 1997, 23: 301-313.
Rousseaux M C, Julkunen T R, Searles P S, Scopel A S, Aphalo P J, Ballarc C L. Solar UV-B radiation affects leaf quality and insect herbivory in the southern beach tree Nothofagus antartica. Oecologia, 2004, 38 (4): 505–512.
Sandmann G, Kuhn S, Boger P. Evaluation of structurally different carotenoids in Escherichia coli transformants as protectants against UV-B radiation. Appl. Environ. Microbiol., 1998, 64: 1972-1974.
Sauter M, Seagull R W, Kende H. Internodal elongation and orientation of cellose microfibrils and microtubules in deepwater rice. Planta, 1993, 190: 354-362.
Savory A. Holistic resource management. Island Press, Covelo California, 1988,564. Scherer S. Recovery of adenine-nucleotide pools in terrestrial blue-green algae after prolong drought periods. Oecologia, 1986, 68: 585-588.
Scherer S, Chen T W, Boger P. A new UV-A/B protecting pigment in the terrestrial cyanobacterium Nostoc commune. Plant Physial.,1988, 88: 1055-1057.
Scherer S, Potts M. Novel water stress- protein from a desiccation-tolerant cyanobacterium.J. Biol. Chem., 1989, 264(21): 12546-12553.
Schindler D W, Curtis J P, Parker B R, Stainton M P. Consequences of climate warming and lake acidification for UV-B penetration in North American boreal lakes. Nature 1996, 379: 705-708.
Schulten J A. Soil aggregation by cryptogams of a sand prairie. J Bot, 1985, 72(11): 1657-1661.
Shalata A, Tal M. The effect of salt stress on lipid peroxidation and antioxidants in the leaf of the cultivated tomato and its wild salt-tolerant relative Lycopersicon pennellii. Physiol. Plant, 1998, 104: 167-174.
Shao Y Q, Zhao J. Study on soil microbial number and soil ecological factor in fixed dunes in the east Hobq sands of NeiMongol. Acta Sci Nat Univ NeiMongol (Nat Sci), 1997, 28 (5): 715-719.
Shibata K. Pigments and a UV-absorbing substance in corals and a blue-green alga living on the Great Barrier Reef. Plant Cell Physiol, 1969, 10: 325-335.
Shields L M, Durrell L W. Algae in relation to soil fertility. Bot. Rev., 1964, 30(1): 92-128.
Siebeck O, et al. Impact of UV-B radiation on zooplankton and fish in pelagic freshwater ecosystems. Arch. Hydrobiol. 1994, 43: 101-114.
Singh N, Asthana R K, Kayastha A M, Pandey S, Chaudhary A K, Singh S P. Thiol and exopolysaccharide production in a cyanobacterium under heavy metal stress. Process Biochemistry, 1999, 35: 63–68.
Sinha R P, Klisch M, Gr?niger A, H?der D P. Ultroviolet-absorbing/screening in cyanobacteria, phytoplankton and macroalgae. J. Photochem. Photobiol. B: Biol, 1998, 47: 82-94.
Sinha R P, Kumar H D, Kumar A, Háder D P. Effects of UV-B irradiation on growth, survival, pigmentation and nitrogen metabolism enzymes in cyanobacteria. Acta Protozool, 1995, 34: 187-192.
Sinha R P, Lebert M, Kumar A, et al. Distintegration of phycobilisomes in a rice field cyanobacterium Nostoc sp. following UV irradiation. J. Photochem. Photobiol. B Boil., 1995, 37(4): 697-706.
Sinha R P, Singh N, Kumar A, et al. Effects of UV irradiation on certain physiological and biochemical processes in cyanobacteria. J. Photochem. Photobiol. B Biol., 1996, 32: 107-113.
Sinha R P, Sinha J P, Groniger A, et al. Polychromatic action spectrum for the induction of a mycosporine-like aminoacid in a rice-field cyanobacterium, Anabaena sp.. J. Photochem. Photobiol. B Biol., 2002, 66: 47-53.
Skarpe C & Henriksson E. Nitrogen fixation by cyanobacterial crusts and by associative-symbiotic bacteria in Western Kalahari, Botswana. Arid Soil Res & Rehabilitation, 1986, 1: 55～59.
Smith D W & Brock T D. The water relations of the alga Cyanidium caldarium in Soil. J. Gen. Microbiol., 1973,127: 74-78.
Smith R C, Prézelin B B, et al. Ozone depletion: ultraviolet radiation and phytoplankton biology in Antarctic waters. Science, 1992, 255: 952-959.
Solheim B, Johanson U, Callaghan T V, et al. The nitrogen fixation potential of arctic cryptogram species is influenced by enhanced UV-B radiation. Oecologia, 2002, 133: 90-93.
Speteac, Hidege, Vassi. The quinone electron acceptors are not the main sensitizers of UV-B induced protein damage in isolated photosystem Ⅱ reaction center and core complexes. Plant Sci., 1996, 115: 207-215.
Stolarski R, Bojkov R, Bishop L. Measured trends in stratospheric ozone. Science, 1992, 56: 342-349.
Strid A. Alteration in expression of defence genes in Pisum sativum after exposure to supplementary ultraviolet-B radiation. Plant Cell Physiol, 1993, 34: 949-953.
Strid A. Alteration in pigment content in leaves of Pisum sativum after exposure to supplementary UV-B. Plant Cell Physiol, 1992, 33 (7): 1015-1023.
Sullivan J H. Effects of increasing UV-B radiation and atmospheric CO2 on photosynthesis and growth: implications for terrestrial ecosystems. Plant ecology, 1997,128: 194-206.
Suresh B G, Joshi P C, Viswanathan P N. UV-B induced reduction in biomass and overall productivity of cyanobacteria. Biochem. Biophys. Res. Commun. 1998, 244: 138-142.
Takeuchia, Yamaguchit, Hidemaj, et al. Changes in synthesis and degradation of Rubisco and LHC Ⅱ with leaf age in rice (Oriza sativa L.) growing under supplementary UV-B radiation. Plant Cell Environ., 2002, 25: 695-706.
Takeuchi Y, Akizuki M, Shimizu H, Kondo N, Sugahara K. Effect of UV-B (290–320 nm) irradiation on growth and metabolism of Cucumber cotyledons. Physiol. Plant. 1989, 76: 425-430.
Takeuchi Y, Kubo H, Kasahara H, et al. Adaptive alteration in activities of scavengers of active oxygen in cucumber cotyledons irradiated with UV-B. J. Plant Physiol, 1996, 147(5): 589-592.
Tchan Y T, Whitehouse J N A. Study of soil algae II. The variation of the soil algal population in sandy soils. Proc. Linn. Soc. New. South Wales, 1953, 78: 160-170.
Tevinim, Iwanzikw, Thomav. Some effects of enhanced UV-B irradiation the growth and composition of plants. Planta, 1981, 153: 388-394.
Tevinim, Teramura A H. UV-B effects on terrestrial plants. Photochem Photobiol, 1989, 50: 479-487.
Tiano P, Accolla P, Tomaselli L. Phototrophic biodeteriogens on lithoid surfaces: An ecological study. Microbiol. Ecol., 1995, 29: 299-309.
Tyagi R, Kumar A, Tyagim B, et al. Protective role of certain chemicals against UV-B-induced damage in the nitrogen-fixing cyanobacterium, Nostoc muscorum. J. Basic Microbiol., 2003, 43: 137-147.
Vaidya B S, Mehta V. Carbohydrates in some blue-green algae. Phykos, 1989, 28: 89-100.
Vassi, Turcsányi, Toulou P, et al. The mechanism of UV-A radiation-induced inhibition of photosystem Ⅱ electron transport studied by EPR and chlorophyll fluorescence. Biochem., 2002, 41: 10200-10208.
Vonshak A, Torzillo G & Tomaseli L. Use of chlorophyll fluorescence to estimate the effect of photoinhibition in outdoor cultures of Spirulina platensis. J Appl Phycol., 1994, 6: 31-34.
Vu C V, Allen L H, Garrard L A. Effects of ebgabced UV-B radiation (280～320 nm) on ribulise-1, 5-bisphos-phate carboxylase in pea and soy bean. Environ Exp Bot, 1983, 23: 150-156.
West N E. Structure and function of microphytic soil crusts in wildland ecosystems of arid to semiarid regions. Advances in Ecological Research, 1990, 20: 179-223.
Willekens H, Vancam P, Vanmontagum, et al. Ozone, sulphur dioxide and UV-B radiation have similar effects on mRNA accumulation of antioxid antgenes in Nicotiana plumbag inifolia L. Plant Physiol, 1994, 106: 1007-1014.
Wingender J, Neu T R, Flemming H C. What are bacterial extracellular polymeric substances? In Wingender J. Neu TR, Flemming H-C (eds), Microbial Extracellular Polymeric Substances. Springer, Berlin. 1999, 1-19.
Wintermans J F G M, Mots D A. Spectrophotometric characteristics of chlorophylls a and b and their pheophytins in ethanol. Biochem Biophys Acta, 1965, 109: 448-453.
Woodall A A, Britton G, Jackson M J. Carotenoids and protection of phospholipids in solution or in liposomes against oxidation by peroxyl radicals: relationship between carotenoid structure and protective ability. Biochim. Biophys. Acta, 1997, 1336: 575-586.
Yan N D, Keller W, Scully N M, Lean D R S, Dillon P. Increased UV-B penetration in a lake owing to drought-induced acidification. Nature, 1996, 381: 141-143.
Yuichi T, Akizuki M, Shimizu H, Kondo N, Sugahara K. Effect of UV-B (290-320 nm) irradiation on growth and metabolism of cucumber cotyledons. Physiol. Plant, 1989, 76: 425-430.
Zaady E, Groffman P, Shachak M. Nitrogen fixation in macro– and microphytic patches in the Negev Desert. Soil B iol & B iochem, 1998, 30: 449-454.
Zak D R, Tilman D. Plant production and soil microorganisms in alter succession ecosystems: a continental-scale study. Ecology, 1994, 75(8): 2333-2347.
Zhang Q, Li N, Zhou G, Lu X, Xu Z, Li Z. In vivo antioxidant activity of polysaccharide fraction from Porphyra haitanesis (Rhodephyta) in aging mice. Pharmacol Res 2003, 48(2): 151-155.
Zhou G F, Sheng W X, Yao W H, Wang C H. Effect of low molecular λ-carrageenan from Chondrus ocellatus on antitumor H-22 activity of 5-Fu. Pharmacological Research, 2006, 53: 129-134.
Ziska L H. The Potential sensitivity of tropical plants to increased Ultraviolet-B radiation. J. Plant Physiol. 1996, 148: 35-41.
Zlotnik I, Dubinsky Z. The effect of light and temperature on DOC excretion by phytoplankton. Limnology and Oceanography, 1989, 34 (6): 831.