典型荒漠苔藓人工繁殖特征与抗御干热环境胁迫的生理生化机制研究
详细信息    本馆镜像全文|  推荐本文 |  |   获取CNKI官网全文
摘要
本文通过调查荒漠苔藓刺叶墙藓组织培养影响因素,探讨了荒漠苔藓及其生物结皮室内快速繁殖可能性,为大规模培养荒漠苔藓以及生物结皮提供基础研究数据;通过调查含水量、叶绿素荧光、电导率、色素含量、超微结构以及再生潜力等传统指标,评价刺叶墙藓对不同脱水速度、不同温度在形态学、生理学以及繁殖生物学等方面的响应,对荒漠地区苔藓生物结皮合理保护与修复具有指导意义;将扫描电镜(SEM)、显微红外(Micro-FTIR)及单次反射(ATR)技术、顺磁共振自选标记(EPR Spin Label)、气质连用(GC/MS)、液质连用(LC/MS)、离子色谱(IC)热动力测定工具(TGA和DSC)、飞行时间质谱(MALDI-TOF)等新技术运用在苔藓耐性研究方面,摸索了刺叶墙藓在表层结构与蜡质化学、细胞内化学成分与凝胶态-液晶态-玻璃态相互转变、细胞膜透性与细胞质分子流动性以及细胞膜界面结构等对不同脱水速度和温度响应,是苔藓生物学研究上新突破,更为研究相对低等且形态较小生物体开辟了一条新途径。同时,运用双向电泳技术,比较了脱水-复水过程中刺叶墙藓蛋白质表达差异,筛选与刺叶墙藓耐干相关功能蛋白,为荒漠苔藓耐干热基因分离及其功能基因在农作物改良中应用奠定基础。
     首先按照组织培养方法调查了几种常见影响因素如消毒方法、培养基、激素、培养温度、外植体、湿度及光照强度与时间等对刺叶墙藓再生的影响。最终确定刺叶墙藓快繁路线为:外植体离体叶片→温度25/15℃→营养源Knop→RH 65-80%→光周期16H→光照强度85-120 PPFD→培养周期2个月,材料无需经过消毒处理;在掌握刺叶墙藓生长影响因素后,尝试构建苔藓结皮:用离体绿叶在20/10℃诱导原丝体,继而转入河砂中,得到原始苔藓结皮,表明苔藓结皮存在人工培育可能。
     为了了解荒漠苔藓对沙漠常见水分和温度胁迫的抗性机制,研究了脱水和高温及联合处理下,刺叶墙藓在形态结构、生理和繁殖特征等方面的响应。形态上刺叶墙藓具有明显的生态优势:①双层细胞壁和脂肪粒含量丰富,其中老化组织比新生组织更具有耐性优势;②快速脱水处理后不同发育阶段的叶片细胞叶绿体变圆,没有出现细胞壁和细胞膜破损;③45℃热处理仅引起叶绿体结构疏松;④45℃干热处理引起叶绿体产生大量气泡且结构扭曲,部分细胞膜破损,表明45℃下脱水和温度对细胞膜存在协同效应;⑤快速脱水、45℃热处理、45℃干热处理后的叶片细胞复水后叶绿体能够恢复正常形态。生理上刺叶墙藓具有明显的抗干热响应:①几种胁迫都引起细胞溶质大量渗漏;②色素和可溶性糖含量仅对热和干热两种处理响应剧烈;③几种胁迫叶绿素荧光活性均降低,但脱水和干热处理后叶片光系统能够快速恢复至正常水平,高温处理(≥50℃)荧光活性丧失,表明极端高温对光系统有致命影响;④高温降低刺叶墙藓再生能力,但干热联合胁迫(<60℃)没有对再生能力产生显著影响;⑤脱水和高温联合处理对生理影响存在两种生态效应,即温度≤45℃二者存在协同作用,温度>45℃脱水对高温效应存在拮抗作用。
     为了进一步阐明刺叶墙藓耐干和耐热根本原因,从结构功能和结构化学方面对其进行了探讨。刺叶墙藓外被蜡纸层,有细胞壁瘤状凸起密布在表面,可以减少水分丧失和阻碍热空气影响,而且蜡质含量高达2.64mg g-1干重,90%以上为长链脂肪酸和烷烃,表明其细胞最外层具有明显生态优势。运用显微红外特征吸收峰揭示了刺叶墙藓化学成分变化与耐热机理存在相关关系。幼嫩组织增加亲水区脂肪和蛋白质含量、提高α-螺旋结构含量,使得细胞结构能够高温下稳定;老化组织通过提高碳氢化合物和疏水区内脂肪含量、稳定蛋白质结构等来维持细胞结构稳定,类似于糖类和蛋白质在脱水过程保护作用。运用顺磁共振自选标记方法研究了细胞膜、细胞质在脱水和干热过程中结构维持特性,刺叶墙藓细胞质稳定主要依靠高含量糖类和生物大分子,在脱水短期内实现玻璃化转变,钝化生理代谢和分子反应活性;依靠具有抗氧化功能两性分子参与膜内,减少或者消除氧自由基对细胞膜损伤,从而保证将脱水时细胞结构损伤降低在可修复范围。
     以上结果表明,刺叶墙藓耐干热除了形态学优势以外,细胞质玻璃化转变在脱水过程对细胞结构具有重要作用。那么再复水过程必然引起大规模细胞溶质渗漏,因此复水后启动损伤修复机制对于刺叶墙藓非常重要。先前研究过程已经证明复水后大量蛋白表达对于修复脱水以及复水造成细胞损伤至关重要。运用双向电泳技术,初步探讨了刺叶墙藓蛋白组学响应,结果发现再复水后新表达或者表达量增加蛋白有脱水素(13.1kDa)、复水蛋白(67.5 kDa)、热激蛋白(71.4 kDa和71.2 kDa)以及小分子热激蛋白(36.7 kDa),其中脱水素和复水蛋白已经在其它生物中证明与耐干性有关,热激蛋白已经证明与耐热和耐干有关,因此这些蛋白可能与刺叶墙藓修复机制相关。
In this study, the factors influencing in the tissue culture of a typical desert moss Tortula desertorum were investigated and the possibility of macropropagating the desert moss was assessed. These works were the foundational data for scale of cultivation of desert mosses and for artificial construction of biological soil crusts (BSCs). Through investigation of the changes of water content, Chlorophyll fluorescence, electron conductivity of solution leakage, pigment content, ultrastructure and regeneration potential, some traditional responses of the desert moss was studied, including morphology and physiology and asexual reproduction to different dehydration rates and temperatures. Those indexes could help establish suitable methods for BSCs restoration in semi-arid and arid regions. Some new biophysical methods such as Scanning electron microscopy (SEM), Atomic force microscopy (AFM), Differentiate scanning calorimeter (DSC), Fourier Transform Infrared Spectroscopy (FTIR), Gas chromatography (GC) and Electron paramagnetic resonance (EPR) were firstly used in study of the desiccation tolerance and thermotolerance in desiccation tolerant mosses. The changes of surface structure and wax chemical characteristics, chemical components and state transition, membrane permeability and cytoplasmic molecular mobility under desiccation and heat stress were studied by those instruments. Those methods and results brought a new path for the study of lower and little size of biomaterial. Furthermore, the proteomics of the desert moss T. desertorum under different water content was studied by 2-demension gel electrophoresis (2-D gel). Some expressed proteins were found and identified, and the functions of these proteins were searched in protein database (NCBI and EBI). This step was crucial of choosing right genes relative with desiccation tolerance and thermotolerance and utilizing these genes for improve crops abiotic tolerances.
     At first, effects of media, explants and culture temperatures on regeneration potential of T. desertorum were investigated respectively in this study. The factors of relative humidity, light intensity and photoperiod were optimized through orthogonal test design. The life cycle of desert moss T. desertorum in cultivation was investigated according to the several factors on asexual reproduction. The protocol for macropropagation of T. desertorum according the following: detached leaves→day/night temperature 25/15℃→nutrient source Knop solid-agar medium→RH 65-80%→photoperiod 16h→light intensity 85-120 PPFD→2 months cultivation. No sterilized materials were used in cultivation. An incipient moss-dominated crust was constructed using detached green leaves cultivated at 20/10℃in Knop agar-solid medium for one month and transplanted in river sand under 25/15℃for other month. This process proved that it was feasibility to artificial construction of BSCs for desert restoration.
     In order to improve the abiotic tolerances and ecological functions of BSCs, the main component of BSCs, the desert moss T. desertorum, the responses in morphology, physiology and reproduction to the extreme environment, especially water and temperature, were investigated. The elder tissues had more advantages in cellular structure to cope with environmental stresses. In dehydration and thermostress and the combined stress test, cellular wall and membrane were not penetrated under fast dry. Only did chloroplasts change loose under 45℃treatment. Plenty of bladders emerged in chloroplasts and membranes were penetrated resulting in lipids transferred from cell inner after tissues were exposed to a combined stress of desiccation and thermostress. Increase of solution leakage, decrease of chlorophyll fluorescence activity, intense responses of pigment and sugars were observed when tissues were subjected to fast dry or higher temperatures. However, the fast recovery could be seen in tissues treated with desiccation or the combined stress after being re-irrigated. Meanwhile, higher temperature (> 30℃) could depressed the leaf regeneration potential but the combined stress (<60℃) have not significant effect on reproduction. These results indicated T. desertorum have desiccation tolerance and thermotolerance.
     To grasp the root cause of desiccation tolerance and thermotolerance of T. desertorum, the structure functions and structural chemistry were studied. There overloaded waxes in the surface between cell membrane and environment. Cell wall stretched outside and formed closed papilla, which could retard water loss and alleviate the damage of hot air. All these information proved the ecological advantages of T. desertorum. The relationship between the changes of chemical components in moss tissues and the mechanisms of thermotolerance were investigated by micro-FTIR. Increase of lipids in hydrophilic regions and proteins content, improvement the structure content ofα-helix in the younger was employed in coping with thermal stress and sustaining the stability of cell structures. The elder engaged with thermostress by promoting the content of carbohydrate and lipids in hydrophobic regions to stabilize the normal structures of proteins and cells. Using different spin labels, the changes of membrane permeability and fluidity and cytoplasmic molecular mobility under desiccation and heat were monitored by EPR. The results elucidated the mechanism of structure stability of cellular membrane and subcellular organelles. T. desertorum depended on high content of sugars and other bio-macromolecules to changes the cytoplasmic state from liquid crystalline to vitrification rapidly after cell lost majority of free water. The rate of metabolism and the activity among molecules were suppressed in glass state, and the substances in cytoplasm were sustained. The partitioning behaviors of amphiphiles could transfer some antioxidants into membrane and eliminated the damage of free radicals. Those processes could maintain the cellular damage within recovery regimes during fast dry.
     Because of vitrification, the cellular structure was stability and the solution leakage during rehydration became serious. There need powerful recovery mechanism to resume the normal function of cell. The former reports had proposed that the proteins expressed in rehydration were the key to repair the damage of moss in dehydration and rehydration. Some different expression proteins were found between dried and re-wet materials using 2-D gel. Especially, the content of dehydrin (13.1kDa), rehydrin (67.5 kDa), HSP 70 (71.4 kDa和71.2 kDa) and sHSP (36.7 kDa) were up regulation during rehydration and we believed those proteins and corresponding genes had a role in repair mechanism.
引文
[1] Gaff, D.F. Mechanisms of desiccation tolerance in resurrection vascular plants. In: Basra AS and Basra RK (eds) (Mechanisms of Environmental Stress Resistance in Plants). Harwood Academic Publishers, London. 1997: 43–58.
    [2] Oliver MJ, Bewley JD. Desiccation-tolerance of plant tissues: a mechanistic overview. Horticultural Reviews. 1997, 18: 171-214
    [3] Potts M. Desiccation tolerance of prokaryotes. Microbiology Review. 1994, 58: 755-805
    [4] Dodds WK, Gudder DA, Mollenbauer D. The ecology of Nostoc. Journal of Phycology. 1995, 31: 2-18
    [5] Alpert P. The limits and frontiers of desiccation-tolerant life. Integr. Comp. Biol. 2005, 45: 685-695
    [6] Oliver, MJ, Velten J, Mishler B. Desiccation tolerance in bryophytes: a reflection of the primitive strategy for plant survival in dehydrating habitats? Integr. Comp. Biol. 2005,45: 788 -799
    [7] Mundree SG, Baker B, Mowla S, et al. Physiological and molecular insights into drought tolerance. African Journal of Biotechnology. 2002, 1(2): 28-38
    [8] Watanabe M, Kikawada T, Okuda T. Increase of onternal ion concentration triggers trehalose systhesis associated with cryptobiosis in larvae of Polypedilum vanderplanki. The journal of experimental biology. 2003, 206: 2281-2286
    [9] Goyal K, Walton LJ, Tunnacliffe A. LEA proteins prevent protein aggregation due to water stress. Biochem J. 2005, 338: 151-157
    [10] Ingram J, Bartel D. The molecular basis of dehydration tolerance in plants. Annual Review of Plant Physiology and Plant Molecular Biology. 1996, 47: 377-403
    [11] Pammenter NW, Berjak P.A review of recalcitrant seed physiology in relation to desiccation – tolerance mechanisms. J. Seed Sci. Res. 1999 , 9: 13-37
    [12] Galau GA, Jakobsen KS, Hughes DW. The controls of late dicot embryogenesis and early germination. J. Physiol. Plant. 1991, 81: 280-288
    [13] Vertucci CW, Farrant JM, 1995. Acquisition and loss of desiccation tolerance. In Kigel J and Galili G (eds) (Seed Development and Germination). New York: Marcel Dekker Inc. 1995: 237 —271
    [14] Kermode AR, Finch-Savage BE. Desiccation sensitivity in orthodox and recalcitrant seed in relation to development. In Black M and Pritchard HW (eds) (Desiccation andsurvival in Plant: Drying without Dying).Oxon: CABI Publishing. 2002: 149-184
    [15] Vertucci CW, Roos EE. Theoretical basis of protocols for seed storage II. The influence of temperature on optimal moisture contents. J. Seed Sci. Res. 1993, 3: 201 -213
    [16] Hoekstra FA, Golovina EA, Buitink J. Mechanisms of plant desiccation tolerance. Trends Plant Sci. 2001, 6: 431-438
    [17] Crowe, J.H., Hoekstra, F.A. and Crowe, L.M. Anhydrobiosis. Annual Review of Physiology. 1992, 54: 579–599
    [18] Hoekstra FA. Differential longevities in desiccated anhydrobiotic plant systems. Integr. Comp. Biol. 2005, 45: 725 -733
    [19] Halliwell B. Oxidative damage, lipid peroxidation and antioxidant protection in chloroplasts. Chem. Phys. Lipids. 1987, 44:327-340.
    [20] Smirnoff N. The role of active oxygen in the response of plants to water deficits and desiccation. New Phytol. 1993, 125:27-58
    [21] Farrant JM. A comparison of mechanisms of desiccation tolerance among three angiosperm resurrection plant species. Plant Ecol. 2000, 151:29-39
    [22] Gaff DF. Responses of desiccation tolerant "resurrection" plants to water stress. In Kreeb KH et al (eds) (Structural and functional responses to environmental stresses: water shortages). SPB Academic Publishing, The Hague, Netherlands. 1989: 264-311
    [23] Oliver MJ, Woods AJ, O’Mahony P. “To dryness and beyond” preparation for the dried state and rehydration in vegetative desiccation-tolerant plants. Plant Growth Regul. 1998, 24:193-210
    [24] Lawlor DW, Cornic G. Photosynthetic carbon assimilation and associated metabolism in relation to water deficits in higher plants. Plant Cell Environ. 2002, 25: 275-294
    [25] Vander Willigen C, Pammenter NW, Mundree SG, Farrant JM. Some Physiological comparisons between the resurrection grass, Eragrostis nindensis, and the related desiccation-sensitive species, Eragrostis curvula. Plant Growth Regul. 2001, 35:121-129
    [26] Mundree SG, Whittaker A, Thomson JA, et al. An aldose reductase homolog from the resurrection plant Xerophyta viscosa Baker. Planta. 2000, 211: 693-700
    [27] Vander Willigen C, Mundree SG, Farrant, JM. Tonoplast intrinsic proteins in the resurrection grass, Eragrostis nindensis. Gordon Conference, Oxford, UK. 2000
    [28] Sherwin HW, Farrant JM. Protection mechanisms against excess light in the resurrection plants Craterostigma wilmsii and Xerophyta viscosa. Plant Growth Regul. 1998, 24:203-210.
    [29] Kranner I, Beckett RP, Worknik S, Zorn M, Pfeifhofer W (2002). Antioxidants help theresurrection plant Myrothamnus flabellifolia survive desiccation. Plant J. 30:1-13
    [30] Blackman SA, Obendorf RL, Leopold AC. Maturation proteins and sugars in desiccation tolerance of developing soybean seeds. J. Plant Physiol.1992, 100: 225-230
    [31] Mowla SB, Thomson JA, Farrant JM, et al. A novel stress-inducible antioxidant enzyme identified from the resurrection plant Xerophyta viscosa Baker. Planta. 2002, 215:716-726
    [32] Kang SW, Chae HZ, Seo MS, et al. Mammalian peroxiredoxin isoforms can reduce hydrogen peroxide generated in response to growth factors and tumor necrosis factoralpha. J. Biol Chem. 1998, 273: 6297-6302
    [33] Goldmark PJ, Curry J, Morris CF, et al. Cloning and expression of an embryo-specific mRNA up-regulated in hydrated dormant seeds. Plant Mol. Biol. 1992, 19: 433-441
    [34] Lee KO, Jang HH, Jung BG, et al. Rice 1Cys-proxiredoxin overexpressed in transgenic tobacco does not maintain dormancy but enhances antioxidant activity. FEBS Lett. 2000, 486:103-106
    [35] Oliver MJ, Tuba Z, Mishler BD. The evolution of vegetative desiccation tolerance in land plants. Plant Ecology. 2000, 151: 85–100
    [36] Proctor MCF, Smirnoff N. Rapid recovery of photosystems on rewetting desiccation-tolerant mosses: chlorophyll fluorescence and inhibitor experiments. J Exp. Bot. 2000, 51:1695 1704
    [37] Bewley JD, Halmer P, Krochko JE, et al. Metabolism of a drought-tolerant and a drought-sensitive moss: respiration, ATP synthesis and carbohydrate status. In Crowe JH and Clegg JS (eds) (Dry Biological Systems). Academic Press, New York. 1978: 185–203
    [38] 郭水良,曹同. 苔藓植物生态学研究进展. 浙江师范大学报(自然科学版). 2000, 23: 291-296
    [39] 吴玉环,黄国宏,高谦等. 苔藓植物对环境变化的响应及适应性研究进展. 应用生态学报. 2001, 12: 943-946
    [40] 张萍,白学良,钟秀丽.苔藓植物耐旱机制研究进展. 植物通报. 2005,22: 107-114
    [41] Tucker EB, Costerton JW, Bewley JD. The ultrastructure of the moss Tortula ruralis on recovery from desiccation.Can.J.Bot. 1975, 53:94–101
    [42] Oliver MJ, Bewley JD. Desiccation and ultrastructure in bryophytes. Advances in Bryology. 1984a, 2: 91–131
    [43] Platt KA, Oliver MJ, Thomson WW. Membranes and organelles of dehydrated Selaginella and Tortula retain their normal configuration and structural integrity:Freeze fracture evidence. Protoplasma. 1994, 178:57–65
    [44] Oliver MJ, Wood AJ, O’Mahony P. How some plants recover from vegetative desiccation: A repair based strategy. Acta Physiologia Plantarum. 1997, 19: 419–425
    [45] Wood AJ, Oliver MJ. Translational control in plant stress: the formation of messenger ribonucleoprotein particles (mRNPs) in response to desiccation of Tortula ruralis gametophytes. The Plant Journal. 1999, 18: 359–370.
    [46] Wood AJ, Duff RJ, Oliver MJ. Expressed sequence tags (ESTs) from desiccated Tortula ruralis identify a large number of novel plant genes. Plant and Cell Physiology. 1999, 40: 361–368
    [47] Velten J, Oliver MJ. Tr288, a rehydrin with a dehydrin twist. Plant Molecular Biology. 2001, 45: 713-722
    [48] Peng CA, Oliver MJ, Wood AJ. Is the Rehydrin TrDr3 from Tortula ruralis associated with tolerance to cold, salinity, and reduced pH? Physiological evaluation of the TrDr3-orthologue, HdeD from Escherichia coli in response to abiotic stress. Plant Biol (Stuttg). 2005, 7(3): 315-320
    [49] Wise MJ, Tunnacliffe A. POPP the question: what do LEA proteins do? Trends Plant Sci. 2004, 9:13-17
    [50] Bartels D, Nelson D. Approaches to improve stress tolerance using molecular genetics. Plant, Cell and Environment. 1994, 17: 659–667
    [51] Baker J, Steele C, Dure? L. Sequence and characterization of 6 Lea proteins and their genes from cotton. Plant Mol. Biol. 1988, 11: 277~291
    [52] Desprez T, Amselem J, Caboche M, et al. Differential gene expression in Arabidopsis monitored using cDNA arrays. Plant J. 1998, 14:643-652
    [53] Dure? L. A repeating 112 meramino acid motif and plant desiccation. Plant J. 1993, 3: 363-369
    [54] Hong B, Barg R, Ho DT. Developmental and organ specific expression of an ABA and stress induced protein in barley. Plant Mol. Biol. 1992, 18: 663-674
    [55] Sivamani E, Ahmed B, Wraith M, et al. Improved biomass productivity and water use efficiency under deficit condition in transgenic wheat constitutively expressing the barley HVA1 gene. Plant Sci. 2000, 155: 1-9
    [56] Xu D,Duan X,Wang B, et al. Expression of a late embryogenesis abundant protein gene, HVA1, from barley confers tolerance to water deficit and salt stress in transgenic rice. Plant Physiol. 1996, 110: 249-257
    [57] Momma M, Kaneko S, Haraguchi K, et al. Peptide mapping and assessment of cryoprotective activity of 26/27-kDa dehydrin from soybean seeds. Biosci. Biotechnol. Biochem. 2003, 67: 1832-1835
    [58] Close T. A commonality in the response of plants to dehydration and low temperature. Physiologia Plantarum. 1997, 100: 291–296
    [59] Schaffner AR. Aquaporin function, structure, and expression: are there more surprises to surface in water relations? Planta.1998, 204: 131-139
    [60] Guerrero FD, Jones JT, Mullet JE. Turgor-responsive gene transcription and RNA levels increase rapidly when pea shoots are wilted. Sequence and expression of three inducible genes. Plant Mol Biol. 1990, 15: 11-26
    [61] Seki M, Narusaka M, Ishida J, et al. Monitoring the expression profiles of 7000 Arabidopsis genes under drought, cold and high-salinity stresses using a full-length cDNA microarray. Plant J. 2002, 31:279-292
    [62] Barrieu F, Marty-Mazars D, et al. Desiccation and osmotic stress increase the abundance of mRNA of the tonoplast aquaporin BobTIP26-1 in cauliflower cells. Planta.1999, 209: 77-86
    [63] Li L, Li S, Tao Y, et al. Molecular cloning of a novel water channel from rice: its products expression in Xenopus oocytes and involvement in chilling tolerance. Plant Sci. 2000, 154: 43-51
    [64] Leone A, Tucci CM, Grillo S. Comparative analysis of short- and long-term changes in gene expression caused by low water potential in potato (solanum tuberosum) cell-suspension cultures. Plant Physiol. 1994, 106: 703–712
    [65] Kononowicz AK, Nelson DE, Singh NK, et al. Regulation of the Osmotin Gene Promoter. Plant Cell. 1992 , 4: 513-524
    [66] Nelson DE, Raghothama KG, Singh NK, et al. Analysis of structure and transcriptional activation of an osmotin gene. Plant Mol. Biol. 1992, 19: 577-88
    [67] 徐平,凌建群,李德葆.一种新与渗调蛋白基因启动子结合蛋白基因分离.中国科学(C 辑). 1999, 29:68-74
    [68] Raghothama KG, Liu D, Nelson DE, et al. Analysis of an osmotically regulated pathogenesis-related osmotin gene promoter. Plant Mol. Biol. 1993, 23: 1117-1128
    [69] 王志珍.蛋白质折叠和分子伴侣.生物学通报, 2004, 39(5): 1-6
    [70] Wehmeyer N, Vierling E. The expression of small heat shock proteins in seeds responds to discrete developmental signals and suggests a general protective role in desiccation tolerance. Plant Physiol. 2000, 122:1099-1108
    [71] Opbrien MC, Flaherty KM, McKay DB. Lysine 71 of the chaperone protein Hsc70 is essential for ATP hydrolysis. J. Biol. Chem. 1996, 271: 15874-15878
    [72] 宋松泉, Fredlund KM, Mqller IM 等. 脱水胁迫对吸胀甜菜种子萌发行为和线粒体小分子量热休克蛋白影响. 中山大学学报(自然科学版). 2001, 40: 79-83
    [73] Alamillo J, Almoguera C, Bartels D, et al. Constitutive expression of small heat shock proteins in vegetative tissues of the resurrection plant Craterostigma plantagineum. Plant Mol. Biol. 1995, 29: 1093-1099
    [74] Shen GA, Pang YZ, Lin CF, et al.. Cloning and characterization of a novel Hsp100/Clp gene (osClpD) from Oryza sativa. DNA Seq. 2003, 14: 285-293
    [75] Leopold AC, Sun WQ, Bernal-Lugo I. The glassy state in seeds: analysis and function. Seed Science Research. 1994, 4: 267–274.
    [76] Sun WQ, Leopold AC. Cytoplasmic vitrification and survival of anhydrobiotic organisms. Comparative Biochemistry and Physiology. 1997, 117A: 327–333
    [77] Crowe JH, Hoekstra FA, Crowe LM. The role of vitrification in anhydrobiosis. Annu. Rev. Physiol. 1998, 60:73–103
    [78] Buitink J, Hemmings MA, Hoekstra FA. Is there a role for oligosacharrides in seed longevity? An assessment of intracellular glass stability. Plant Physiology. 2000, 122: 1217–1224.
    [79] Avonce N, Leyman B, Thevelein J, et al. Trehalose metabolism and glucose sensing in plants. Biochem. Soc. Trans. 2005, 33: 276-279
    [80] Bewley JD, Krochko JE. Desiccation-tolerance. In Lange OL et al (eds) (Encyclopedia of Plant Physiology Vol12B, Physiological Ecology II). Springer-Verlag, Berlin. 1982: 325–378
    [81] Boubriak I, Kargiolaki H, Lyne L, et al. The requirement for DNA repair in desiccation tolerance of germinating embryos. Seed Sci. Res. 1997, 7: 97-105
    [82] O’Mahony P, Oliver MJ. Characterization of a desiccation responsive small GTP-binding protein (Rab2) from the desiccation tolerant grass Sporobolus stapfianus. Plant Molecular Biology. 1999a, 39:809–821
    [83] O’Mahony P, Oliver MJ. The involvement of ubiquitin in vegetative desiccation-tolerance. Plant Molecular Biology. 1999b, 41:657–667
    [84] Qin Z, Chen XB, Wood AJ. Two early light-induced proteins (ELIP)cDNAs from the resurrection plant Tortula rarulis are differentially expressed in response to desiccation , rehydration, salinity, and high light. Journal of exp.Bot. 2002, 371: 1197-1205
    [85] Belnap J. Surface disturbances: their role in accelerating desertification. Environ Monit Assess. 1995, 37: 9–57
    [86] Belnap J. Microbes and microfauna associated with biological soil crusts. In: Belnap J, Lange OL (eds) (Biological soil crusts: structure, function, and management). Springer, Berlin. 2003: 128–300
    [87] Grettarsdottir J, Aradottir AL, Vandvik V, et al. Long term effects of reclamationtreatments on plant succession in Iceland. Restoration Ecology. 2004, 12: 268–278
    [88] Hawkes CV. Nitrogen cycling mediated by biological soil crusts and arbuscular mycorrhizal fungi. Ecology. 2003, 84: 1553 - 1562
    [89] Belnap J. Nitrogen fixation in biological soil crusts from southeast Utah, USA. Biol. Fertil. Soils. 2002, 35: 128–135
    [90] Belnap J, Lange O L. Biological soil crusts: structure, function and management, Ecological Studies. Vol 150, Springer Berlin,Heidelberg, New York. 2001:304-314
    [91] Warren S. Synopsis: influence of biological soil crusts on arid land hydrology and soil stability. In: Belnap J and Lange O (eds) (Biological Soil Crusts: Structure, Function, and Management). Springer-Verlag, Berlin, Heidelberg. 2001: 349–360.
    [92] Reynolds R, Belnap J, Reheis M, et al. Aeolian dust in Colorado Plateau soils: nutrient inputs and recent change in source. Proc. Natl. Acad. Sci. USA. 2001, 98: 7123–7127.
    [93] Cove D, Benzanilla M, Harries P, et al. Mosses as Model Systems for the Study of Metabolism and Development. Annu Rev Plant Biol. 2006, 57: 497–520
    [94] Frank W, Decker EL, Reski R. Molecular tools to study Physcomitrella patens. Plant Biology (Stuttgart, Germany). 2005, 7: 220-227
    [95] Duckett, JG, Burch J, Fletcher PW, et al. In vitro cultivation of bryophytes: a review of practicalities, problems, progress and promise. Journal of Bryology. 2004, 26: 3 – 20
    [96] Hohe A, Reski R. From axenic spore germination to molecular farming one century of bryophyte in vitro culture. Plant Cell Reports. 2005, 23: 513 – 521
    [97] Reski R. Physcomitrella and Arabidopsis: the David and Goliath of reverse genetics. Trends Plant Sci. 1998, 3: 209–210
    [98] Reski R. Molecular genetics of Physcomitrella. Planta. 1999, 208: 301–309
    [99] Wood AJ, Oliver MJ, Cove DJ. Bryophytes as model systems. Bryologist. 2000, 103: 128–133
    [100] Schaefer DG. Gene targeting in Physcomitrella patens. Current Opinion in Plant Biology. 2001, 4: 143-150
    [101] Bewley JD. The effects of liquid nitrogen temperatures on protein and RNA synthesis in the moss Turtula ruralis. Plant Sci. Letters. 1973, 1:303-308.
    [102] Saavedra L, Svensson J,Carballo V, et al. A dehydrin gene in Physcomitrella patens is required for salt and osmotic stress tolerance. Plant J. 2006,45(2): 237-249
    [103] Lunde C, Baumann U, Shirley NJ, et al. Gene structure and expression pattern analysis of three monodehydroascorbate reductase (Mdhar) genes in Physcomitrella patens: implications for the evolution of the MDHAR family in plants. Plant Mol. Biol. 2006, 60: 259–275
    [104] 白学良,王瑶,徐杰等. 沙坡头地区固定沙丘结皮层藓类植物繁殖和生长特性研究.中国沙漠. 2003,32(2): 171-176
    [105] Bowker M, Stark LR, McLetchie DN, et al. Sex expression, skewed sex ratios, and microhabitat distribution in the dioecious desert moss Syntrichia caninervis (Pottiaceae). American Journal of Botany. 2000, 87: 517 - 526
    [106] Stark, LR, Nichols II L, McLetchie DN, et al. Age and sex - specific rates of leaf regeneration in the Mojave Desert moss Syntrichia caninervis. American Journal of Botany. 2004, 91: 1 - 9
    [107] 聂华丽,吴楠,梁少民等. 不同沙埋深度对刺叶墙藓植株碎片生长影响. 干旱区研究. 2006, 23: 66-70
    [108] Stark LR, McLetchie DN. Gender - specific heat - shock tolerance of hydrated leaves in the desert moss Syntrichia caninervis. Physiologia Plantarum. 2006, 126: 187 - 195
    [109] Stark LR, McLetchie DN, Mishler BD. Sex expression, plant size, and spatial segregation of the sexes across a stress gradient in the desert moss Syntrichia caninervis. Bryologist. 2005a, 108: 183 - 193
    [110] Stark LR, Nichols II L, McLetchie DN, et al. Do the sexes of the desert moss Syntrichia caninervis differ in desiccation tolerance? A leaf regeneration assay. International Journal of Plant Sciences. 2005b, 166: 21 - 29
    [111] Bopp M. Developmental physiology of bryophytes. In: Schuster RM (ed) (New Manual of Bryology). Hattori Botanical Laboratory, Tokyo, Japan. 1983: 276 – 324
    [112] 南京农业大学.土壤农化分析(第2版).北京: 农业出版社,1994
    [113] Xuan XM, Wang Y, Cai WM. An application of orthogonal design in soil culture of Tortula desertorum. Shanghai Environmental Sciences. 2004a, 23: 13 - 15
    [114] Xuan XM, Wang Y, Cai WM. Primary tissue culture of Tortula desertorum using orthogonal design. Biotechnology. 2004b, 14(3): 32 - 33
    [115] Schumaker KS, Dietrich MA. Hormone - induced signaling during moss development. Annu.Rev. Plant Physiol. Plant Mol. Biol. 1998, 49: 501 – 523
    [116] Zhang YM, Cao T, Pan BR. A study on bryophyte associated with formation of soil crust in south fringe of Gurbantunggut Desert in Xinjiang. Acta Botanica Boreali occidentalia Sinica. 2002, 22: 18 - 23
    [117] Levitt J. Responses of plants to environmental stresses. Vol. I. Chilling, freezing, and high temperature stresses. Academic Press, New York. 1980
    [118] Oliver MJ. Desiccation-tolerance in plant cells. A mini review. Plant Physiology. 1996, 97: 779-787
    [119] Gaff DF, Loveys BR. Abscisic acid content and effects during dehydration ofdetached leaves of desiccation-tolerant plants. Journal of Experimental Botany. 1984, 35: 1350–1358
    [120] Tuba Z, Proctor MCF, Csintalan Z. 1998. Ecophysiological responses of homoiochlorophyllous and poikilochlorophyllous desiccation-tolerant plants: a comparison and ecological perspective. Plant Growth Regulation. 1998, 24: 211–217
    [121] Cooper K, Farrant JM. Recovery of the resurrection plant Craterostigma wilmsii from desiccation: protection vs repair. Journal of Experimental Botany. 2002, 53: 1805-1813
    [122] Cooper RL, Martin RJ, St. Martin SK,et al. Registration od ‘Stressland’ soybean. Crop Sci. 1999, 39:590–591
    [123] Proctor MCF, Pence VC. Vegetative tissue: bryophytes,vascular resurrection plants and vegetative propagules. In Black M and Pritchard HW (eds) (Desiccation and survival in plants). Drying without dying. CABI Publishing, Wallingford, OX, UK. 2002: 207-230
    [124] Liu Y, Li Z, Cao T, et al. The influence of high temperature on cell damage and shoot survival rates of Plagiomnium acutum. Journal of Bryology. 2004, 26: 265–271.
    [125] Hearnshaw GF, Proctor MCF. The effect of temperature on the survival of dry bryophytes. New Phytologist. 1982, 90: 221–228
    [126] Carballeira A, Díaz S, Vázquez MD, et al. Inertia and resilience in the response of the aquatic bryophyte Fontinalis antipyretica Hedw to thermal stress. Archives of Environmental Contamination and Toxicology. 1998, 34: 343–349
    [127] Liu Y, Cao T, Xiang F, et al. Effect of high temperature stress on the activity of peroxidase of two species of mosses. Guihaia. 2001, 21: 255–258
    [128] 张显强, 罗在柒, 唐金刚等. 高温和干旱胁迫对鳞叶藓游离脯氨酸和可溶性糖含量影响. 广西植物. 2004, 24(6): 570~573
    [129] McLetchie DN, Stark LR. Sporophyte and gametophyte generations differ in their thermotolerance response in the moss Microbryum. Annals of Botany. 2006, 97: 505-511
    [130] Georgieva K, Maslenkova L, Peeva V, et al. Comparative study om the changes in photosynthetic activity of the homoiochlorophyllous desiccation-tolerant Haberlea rhodopensis and desiccation-sensitive spinach leaves during desiccation and rehydration. Photosynthesis research. 2005, 85: 191-203
    [131] Sherwin HW, Farrant JM. Differences in three resurrection plants angiosperms species. Ann. Bot. 1996, 78: 703-710.
    [132] Leprince OG, Hendry AF, McKersie BM. The mechanisms of desiccation tolerance in developing seeds. Seed Sci. Res. 1993, 3: 231–246.
    [133] Alpert P, Oliver MJ. Drying without dying. In Black M, Pritchard HW, eds, Desiccation and survival in plants. Drying without dying. CABI Publishing, Wallingford, OX, UK. 2002: 4-31
    [134] Sun WQ (2002) Methods for the study of water relations under desiccation stress. In Black M, Pritchard HW (eds) (Desiccation and survival in plants). Drying without dying. CABI Publishing, Wallingford, OX, UK, p 47-79
    [135] Pammenter NW, Berjak P, Wesley-Smith J et al. Experimental aspects of drying and recovery. In: M. Black and H.W. Pritchard (eds) (Desiccation and Survival in Plants: Drying Without Dying). CABI, Wallingford, UK. 2002: 93–110
    [136] Murray MB, Cape JN, Fowler D. Quantification of frost damage in plant tissues by rates of electrolyte leakage. New Phytol. 1989, 113: 307-311
    [137] Beckett RP, Marschall M, Laufer Z. Hardening enhances photoprotection in the moss Atrichum androgynum during rehydration by increasing fast- rather than slow-relaxing quenching. Journal of bryology. 2005, 27: 7-12
    [138] Hoekstra FA, Golovina EA. The role of amphiphiles. Comp. Biochem. Physiol. 2002, 131A: 527-533
    [139] Smirnoff N. The carbohydrates of bryophytes in relation to desiccation tolerance. J. Bryol. 1992, 17(3): 185~191
    [140] Strauss G, Hauser H. Stabilization of lipid bilayer vesicles by sucrose during freezing. Proc. Natl. Acad. Sci. USA. 1986, 83: 2422-2426
    [141] Bewley JD, P Halmer, JE Krochko, et al. 1978 Me- tabolism of a drought-tolerant and a drought-sensitive moss: respiration, ATP synthesis and carbohydrate status. In JH Crowe and JS Clegg (eds) (Dry Biological Systems). Academic Press, New York. San Francisco London.1978: 185-203
    [142] Bewley JD. Polyribosomes conserved during desiccation of the moss Tortula ruralis are active. Plant Physiol.1973, 51: 285-288
    [143] Yordanov I, Tsonev T, Goltsev V, et al. Gas exchange and chlorophyll fluorescence during water and high temperature stresses and recovery. Probable protective effect of carbamide cytokinin 4-PU30. Photosynthetica. 1997, 33: 423–431.
    [144] Jiang Y, Huang B. Effects of drought or heat stress alone and in combination on Kentucky bluegrass. Crop Sci. 2000, 40: 1358–1362
    [145] Chen CF, Liang ZD, Wang HS. Physiological responsesof perennial ryegrass to high temperature and drought. J Nanjiang Agric Univ. 1988, 11: 87–92.
    [146] Alpert P, Oechel WC. Carbon balance limits the microdistribution of Grimmia laevingata, a desiccation tolerant plant. Ecology. 1985, 66: 660~669
    [147] Tuba Z, Csintalan Zs, Proctor MCF. Photosynthetic responses of a moss,Tortularuralis, ssp.ruralis, and the lichens Cladonia convoluta and C. furcata to water deficit and short periods of desiccation, and their ecophysiological significance: a base line study at present-day CO2 concentration. New Phytol.1996, 133: 353–361.
    [148] Hamerlynck EP, Huxman TE, Loik ME, et al. Effects of extreme high temperature, drought and elevated CO 2 on photosynthesis of the Mojave Desert evergreen shrub, Larrea tridentata. Plant Ecology. 2000, 148:185-195.
    [149] Minibayeva F, Beckett RP. High rates of extracellular superoxide production in bryophytes and lichens, and an oxidative burst in response to rehydration following desiccation. New Phytologist. 2001, 152: 333-343
    [150] Gilmore AM. Mechanistic aspects of xanthophyll cycle-dependant photoprotection in higher plant chloroplasts and leaves. Phsiol. plantarum. 1997, 99: 197-209
    [151] Beckett RP. ABA-induced tolerance to ion leakage during rehydration following desiccation in the moss Atrichum androgynum. Plant growth regulation. 2001, 35: 131-135
    [152] Mayaba N, Beckett RP, Csintalaa Z, et al. ABA increases the desiccation tolerance of photosynthesis in the aftomontane understorey Moss Atrichum androgynum. Annals of Botany, 2001, 88:1 093-1 100
    [153] Foyer CH, Descourvieres P, Kunert KJ. Protection against oxygen radicals: an important defence mechanism studied in transgenic plants. Plant Cell Eviron. 1994, 17: 507-523.
    [154] Shi YF, Shen YP. Signal, impact and outlook of climatic shift from warm-dry to warm-humid in northwest China. Science & Technology Review. 2003, 21:54-57
    [155] Oliver MJ, Velten J, Wood AJ. Bryophytes as experimental models for the study of environmental stress tolerance: Tortula ruralis and desiccation-tolerance in mosses. Plant Ecology. 2000, 151: 73-84
    [156] Beckett RP, Mayaba N, Minibayeva FV, et al. Hardening by partial dehydration and ABA increase desiccation tolerance in the cyanobacterial lichen Peltigera polydactylon. Annals of Botany. 2005b, 96(1): 109–115
    [157] Bewley JD. Physiological aspects of desiccation tolerance. Annual Review of Plant Physiology and Plant Molecular Biology. 1979, 30:195-238
    [158] Hoekstra FA, Wolkers WF, Buitink J, et al. Membrane stabilization in the dried state. Comp. Biochem. Physiol. 1997, 117A: 335-341.
    [159] Buitink J, Leprince O, Hemminga MA, Hoekstra FA. Molecular mobility in the cytoplasm: An approach to describe and predict lifespan of dry germplasm. Proc. Natl. Acad. Sci. U.S.A. 2000, 97:2385-2390
    [160] Golovina EA, Hoekstra FA. Acquisition of desiccation tolerance in developing wheat embryos correlates with appearance of a fluid phase in membranes. Plant Cell Environ. 2003, 26:1815-1826
    [161] Jeffree CE. Structure and ontogeny of plant cuticles. In: Kerstiens G (eds) (Plant cuticles an integrated functional approach). Oxford UK: BIOS Scientific Publishers Ltd. 1996: 33–82.
    [162] Bargel H, Barthlott W, Koch K, et al. 2003. Plant cuticles: multifunctional interfaces between plant and environment. In: Hemsley AR and Poole I (eds) (Evolutionary physiology at the sub-plant level). London: Academic Press. 2003: 171–187.
    [163] Riederer M, Schreiber L. Waxes—the transport barriers of plant cuticles. In: Hamilton RJ (eds) (Waxes: chemistry, molecular biology and functions). Dundee: The Oily Press. 1995: 131–156.
    [164] Barnes JD, Cardoso-Vilhena J. Interactions between electromagnetic radiation and the plant cuticle. In: Kerstiens G (eds) (Plant cuticles, an integrated functional approach). Oxford: Bios Scientific Publishers. 1996: 157–170.
    [165] Barthlott W, Neinhuis C. Purity of the sacred lotus, or escape from contamination in biological surfaces. Planta. 1997, 202: 1–8
    [166] Eigenbrode SD, Espelie KE. Effects of plant epicuticular lipids on insect herbivores. Annu. Rev. Entomol. 1995, 40: 117-142
    [167] Schoonhoven LM, Jermy T, van Loon JJA. Insect-Plant Biology: From Physiology to Evolution. London: Chapman & Hall. 1998
    [168] Scheirer DC, Dolan HA. Bryophyte leaf epiflora: an SEM. and TEM study of Polytrichum commune Hewd. Am J Bot. 1983, 70: 712-718
    [169] Bergstrom DM, Selkirk PM. Bryophyte propagule banks in a feldmark on Subantarctic Macquarie Island. Arct. Antarct. Alp. Res. 1999, 31:202–208
    [170] Proctor MCF. Surface wax on the leaves of some mosses. J. Bryol. 1979, 10: 531-538.
    [171] Guschina IA, Harwood JL. Lipid metabolism in the moss Rhytidiadelphus squarrosus (Hedw.) Warnst from lead-contaminated and non-contaminated populations. J. Exp. Bot. 2002, 53: 455-463.
    [172] Kupcinskiene E, Huttunen S. Long-term evaluation of the needle surface wax condition of Pinus sylvestris around different industries in Lithuania. Environmental Pollution. 2005, 137: 610-618
    [173] Baker EA. Chemistry and morphology of plant epicuticular waxes. In: Cutler DF, Alvin KL, Price CE (eds) (The plant cuticle). London UK: Academic Press. 1982: 139–165.
    [174] Gülz PG. Epicuticular leaf waxes in the evolution of the plant kingdom. Journal of Plant Physiology. 1994, 143: 453–464.
    [175] Jetter R, Riederer M. Epicuticular crystals of nonacosan-10-ol: in-vitro reconstitution and factors influencing crystal habits. Planta. 1994, 195: 257–270.
    [176] Jetter R, Riederer M. In-vitro reconstitution of epicuticular wax crystals: formation of tubular aggregates by long-chain secondary alkanediols. Botanica Acta. 1995, 108: 111–120.
    [177] Koch K, Barthlott W, Koch S, et al. Structural analysis of wheat wax (Triticum aestivum, c.v. ‘Naturastar’ L.): from the molecular level to three dimensional crystals. Planta. 2006, 223: 258–270.
    [178] VonWettstein-Knowles PM. Genetic control of β-diketone and hydroxy-β- diketone synthesis in epicuticular waxes of barley. Planta. 1972, 106: 113–130.
    [179] Anfodillo T, Pasqua Di Bisceglie D, Urso T. Minimum cuticular conductance and cuticle features of Picea abies and Pinus cembra needles along an altitudinal gradient in the dolomites. Tree Physiology. 2002, 22: 479–487
    [180] Prügel B, Loosveldt P, Garrec JP. Changes in the content and constitution of the cuticular wax of Picea abies (L.) Karst in relation to needle ageing and tree decline in five European forest areas. Trees. 1994, 9: 80–87.
    [181] Markst?dter C, Federle W, Jetter R, et al. Chemical composition of the slippery epicuticular wax blooms on Macaranga (Euphorbiaceae) ant-plants. Chemoecology. 2000, 10:33–40
    [182] Avato P. Chemical genetics of epicuticular wax formation in maize. Plant Physiology and Biochemistry. 1987, 25: 179–190
    [183] Beattie GA, Marcell LM. Effect of alterations in cuticular wax blosynthesis on the physiochemical properties and topography of maize leaf surfaces. Plant, Cell & Environment. 2002, 25: 1–16
    [184] Cameron CB. A phylogeny of the hemichordates based on morphological characters. Can. J. Zool. 2005, 83:196-215
    [185] Aarts MG, Keijzer CJ, Stiekema WJ, et al. Molecular characterization of the CER1 gene of Arabidopsis involved in epicuticular wax biosynthesis and pollen fertility. Plant Cell. 1995, 7: 2115-2127
    [186] Xia Y, Nikolau BJ, Schnable PS. Cloning and characterization of CER2, an Arabidopsis gene that affects cuticular wax accumulation. Plant Cell. 1996, 8:1291-1304
    [187] Hannoufa A, Negruk V, Eisner G, et al. The CER3 gene of Arabidopsis thaliana is expressed in leaves, stems, roots, flowers and apical meristems. Plant J. 1996, 10(3): 459–467
    [188] Pighin JA, Zheng H, Balakshin LJ, et al. Plant cuticular lipid export requires an ABC transporter. Science. 2004, 306: 702-704
    [189] Fiebig A, Mayfield JA, Miley NL, et al. Alterations in CER6, a gene identical to CUT1, differentially affect long-chain lipid content on the surface of pollen and stems. Plant Cell. 2000, 12: 2001–2008
    [190] Broun P, Poindexter P, Osborne E, et al. WIN1, a transcriptional activator of epidermal wax accumulation in Arabidopsis. Proc. Natl. Acad. Sci. USA. 2004, 101: 4706 -4711
    [191] Millar AA, Clemens S, Zachgo S, et al. CUT1, an Arabidopsis gene required for cuticular wax biosynthesis and pollen fertility, encodes a very-long-chain fatty acid condensing enzyme. Plant Cell. 1999, 11(5): 825-838
    [192] Chen XB, Goodwin SM, Boroff VL, et al. Cloning and characterization of the WAX2 gene of Arabidopsis involved in cuticle membrane and wax production. Plant Cell. 2003, 15: 1170-1185
    [193] Todd J, Post-Beittenmiller D, Jaworski JG. KCS1 encodes a fatty acid elongase 3-ketoacyl-CoA synthase affecting wax biosynthesis in Arabidopsis thaliana. Plant J. 1999, 17(2): 119 -130
    [194] Aharoni A, Dixit S, Jetter R, et al. The SHINE clade of AP2 domain transcription factors activates wax biosynthesis, alters cuticle properties, and confers drought tolerance when overexpressed in Arabidopsis. Plant Cell. 2004, 16: 2463-2480
    [195] Sturaro M, Hartings H, Schmelzer E, et al. Cloning and characterization of GLOSSY1, a maize gene involved in cuticle membrane and wax production. Plant Physiol. 2005, 138: 478-488
    [196] Tom Shepherd, D. Wynne Griffiths. The effects of stress on plant cuticular waxes. New Phytologist. 2006, 171(3): 469–499.
    [197] Proctor MCF. Diffusion resistances in bryophytes. In: GraceJ, Ford ED, Jarvis PG. (eds) (Plants and their Atmospheric Environment). Blackwell Scientific Oxford. 1981: 219–229.
    [198] Proctor MCF. Structure and ecological adaptation. in Dyer AF and Duckett JG (eds) (The experimental biology of bryophytes). Academic Press London. 1984: 9-37
    [199] Barthlott W, Neinhuis C, Cutler D, et al. Classification and terminology of plant epicuticular waxes. Botanical Journal of the Linnean Society. 1998, 126: 237–260
    [200] Gülz PG, Müller E, Schmitz K, et al. Chemical composition and surface structures of epicuticular leaf waxes of Ginkgo biloba, Magnolia grandiflora and Liriodendron tulipifera. Z. Naturforsch. 1992, 47:516–526
    [201] Fehling E, Mukherjee KD. Acyl-CoA elongase from a higher plant (Lunaria annua): metabolic intermediates of very-long-chain acyl-CoA products and substrate specificity. Biochim Biophys Acta. 1991, 1082: 239–246.
    [202] Ritchie GA, Short KC, Davey MR. In vitro acclimatization of chrysanthemum and sugar beet plantlet by treatment with paclobutrazol and exposure to reduced humidity. J. Exp. Bot. 1991, 42: 1557–1563.
    [203] Jenks MA, Gaston CH, Goodwin MS, et al. Seasonal variation in cuticular waxes of Hosta genotypes differing in leaf surface glaucousness. Horticultural Science. 2002, 37: 673–677
    [204] El-Otmani M, Coggins JrC W. Fruit development and growth regulator effects on normal alkanes of Washington navel orange fruit epicuticular wax. J. Agric. Food Chem. 1985, 33: 656-663
    [205] Premachandra GS, Saneoka H, Fujita K, et al. Leaf water relations osmotic adjustment,cell membrane stability,epicuticular wax load and growth as affected by increasing water deficits in Sorghum. J. Exp. Bot. 1992, 43:1569-1576
    [206] Levene, BC, Owen MDK. Effect of moisture stress and leaf age on bentazon absorption in common cocklebur (Xanthium strumarium) and velvetleaf (Abutilon theophrasti). Weed Sci. 1995, 43: 7–12
    [207] Bondada, BR, Oosterhuis DM, Murphy JB, et al. Effect of water stress on the epicuticular wax composition and ultrastructure of cotton (Gossypium hirsutum L.) leaf, bract and boll. Environ. Exp. Bot. 1996, 36:61–69
    [208] Jefferson PG., Johnson DA, Asay JH. Epicuticular wax production, water status and leaf temperature in triticale range species of contrasting visible glaucousness. Can. J. Plant Sci. 1989, 69:513–519
    [209] Reed DW, Tukey HB. Light intensity and temperature effects on epicuticular wax morphology and internal cuticle ultrastructure of carnation and brussels sprouts leaf cuticles. J Am Soc Hort Sci. 1982, 107:417–420
    [210] Shepherd T, Robertson GW, Griffiths DW, et al. Effects of environment on the composition of epicuticular wax from kale and swede. Phytochemistry. 1995, 40: 407–417.
    [211] Giese BN. Effects of light and temperature on the composition of epicuticular wax of barley leaves. Phytochemistry. 1975, 14: 921–929
    [212] Welker OA, Haas K. Temperature-dependent micromorphology of epicuticularwax in cabbage (Brassica oleracea var. capitata). J. Appl. Bot. 1999, 73: 99-104
    [213] Shepherd T, Robertson GW, Griffiths DW, et al. Effects of environment on the composition of epicuticular wax esters from kale and swede. Phytochemistry. 1997, 46: 83–96
    [214] Gonzalez R, Paul ND, Percy K, et al. Responses to ultraviolet-B radiation (280 – 315 nm) of pea (Pisum sativum) lines differing in leaf surface wax. Physiologia Plantarum. 1996, 98: 852–860
    [215] Zobayed SMA, Afreen-Zobayed F, Kubota C, et al. Stomatal characteristics and leaf anatomy of potato plantlets cultured in vitro under photoautotrophic and photomixotrophic conditions. In Vitro Cellular and Developmental Biology–Plant. 1999, 35: 183–188
    [216] Mankovska B, Percy K, Karnofsky DF. Impact of ambient trophosheric O-3, CO2, and particulates on the epicuticular waxes of aspen clones differing in O-3 tolerance. Ekologia–Bratislava. 1999, 18: 200–210
    [217] Bacic T, Lynch AH, Cutler D. Reactions to cement factory dust contamination by Pinus halepensis needles. Environmental and Experimental Botany. 1999, 41: 155–166
    [218] Viskari EL, Holopainen T, Karenlampi L. Responses of spruce seedlings to exhaust gas under laboratory conditions–II–ultrastructural changes and stomatal behaviour. Environmental Pollution. 2000, 107: 99–107
    [219] Hooker TS, Millar AA, Kunst L. Significance of the expression of the CER6 condensing enzyme for cuticular wax production in Arabidopsis. Plant Physiology. 2002, 129: 1568–1580
    [220] Pruitt RE, Vielle-Calzada JP, Ploense SE, et al. FIDDLEHEAD, a gene required to suppress epidermal cell interactions in Arabidopsis, encodes a putative lipid biosynthetic enzyme. Proceedings of the National Academy of Sciences of the USA. 2000, 97: 1311–1316
    [221] Suh MC, Samuels AL, Jetter R, et al. Cuticular lipid composition, surface structure, and gene expression in Arabidopsis stem epidermis. Plant Physiol. 2005, 139: 1649–1665
    [222] Cameron KD, Moskal WA, Smart LB. A second member of the Nicotiana glauca lipid transfer protein gene family, NgLTP2, encodes a divergent and differentially expressed protein. Functional Plant Biology. 2006a, 33: 141-152
    [223] Kader JC. Lipid-transfer proteins in plants. Annu. Rev. Plant Physiol. Plant Mol. Biol. 1996, 47: 627–654
    [224] Park CJ, Shin R, Park JM, et al. Induction of pepper cDNA encoding a lipidtransfer protein during the resistance response to tobacco mosaic virus. Plant Mol Biol. 2002, 48: 243–254
    [225] Colmenero-Flores JM, Campos F, Garciarrubio A, et al. Characterization of Phaseolus vulgaris cDNA clones responsive to water deficit: identification of a novel late embryogenesis abundant-like protein. Plant Mol Biol. 1997, 35: 393–405
    [226] Jang CS, Lee HJ, Chang SJ, et al. Expression and promoter analysis of the TaLTP1 gene induced by drought and salt stress in wheat (Triticum aestivum L.). Plant Sci. 2004, 167: 995–1001
    [227] Jung HW, Kim W, Hwang BK. Three pathogen-inducible genes encoding lipid transfer protein from pepper are differentially activated by pathogens, abiotic, and environmental stresses. Plant Cell Environ. 2003, 26: 915–928
    [228] Cameron KD, Teece, MA, Smart LB. Increased accumulation of cuticular wax and expression of lipid transfer protein in response to periodic drying events in leaves of tree tobacco. Plant Physiol. 2006b, 140: 176-183
    [229] Belnap J, Phillips SL, Miller ME. Response of desert biological soil crusts to alterations in precipitation frequency. Oecologia.2004, 141: 306-316
    [230] Barker D, Stark LR, Zimpher J, et al. Evidence of drought-induced stress on biotic crust moss in the Mojave Desert. Plant Cell Environment.2005, 28: 939-947.
    [231] Fang JY, Chen AP, Peng CH. Et al. Changes in forest biomass carbon storage in China between 1949 and 1998. Science.2001, 292: 2320-2322.
    [232] Sheppard PR, Comrie AC, Packin GD, et al. The climate of the US Southwest. Clim. Res.2002, 21: 219–238
    [233] Stark LR, Mishler BD, McLetchie DN. Sex expression and growth rates in natural populations of the desert soil crustal moss Syntrichia caninervis. Journal of Arid Environments.1998, 40: 401–416.
    [234] 张元明. 荒漠地表生物土壤结皮微结构及其早期发育特征.科学通报. 2005,50(1):42-47
    [235] Carballeira A, Díaz S, Vázquez MD. Inertia and resilience in the response of the aquatic bryophyte Fontinalis antipyretica Hedw. to thermal stress. Arch. Environ. Contam. Toxicol.1998, 34: 343–349
    [236] Post A. Photoprotective pigment as an adaptive strategy in the antarctic moss Ceratodon purpureus. Polar Biology. 1990,10(4):241-245
    [237] Liu Y, Cao T, Glime JM. The changes in membrane permeability of mosses under high temperature stress. Bryologist.2003, 106: 53–60
    [238] Surewicz WK, Mantsch HH, Capman D. Determination of protein secondary structure by Fourier transform infrared spectroscopy: a critical assessment.Biochemistry. 1993, 32: 389-394
    [239] Dave N, Troullier A, Mus-Veteau I, et al. Secondary Structure Components and Properties of the Melibiose Permease from Escherichia coli: A Fourier Transform Infrared Spectroscopy Analysis. Biophys. J. 2000, 79: 747-755
    [240] Yang J, Yen H. Early salt stress effects on the changes in chemical composition in leaves of ice plant and Arabidopsis. A fourier transform infrared spectroscopy Study. Plant Physiol. 2002, 130:1032-1042
    [241] Wolkers WF, Tetteroo FAA, Alberda M, et al. Changed properties of the cytoplasmic matrix associated with desiccation tolerance of dried carrot somatic embryos: an in situ Fourier transform infrared spectroscopic study. Plant Physiol. 1999, 120: 153-163
    [242] Wolkers WF, Hoekstra FA. Aging of dry desiccation-tolerant pollen does not affect protein secondary structure. Plant Physiol. 1995, 109: 907-915
    [243] 李艳梅,赵玉芬,郁鉴源等. 环磷腺苷对人血红细胞膜蛋白二级结构影响 FTIR光谱研究. 光谱学与光谱分析.1997,17(6):28-31
    [244] 卞为东; 孙素琴; 黄岳顺等. FTIR 光谱法研究天花粉蛋白热去折叠过程.光谱学与光谱分析. 2000,20(4):471-473
    [245] 东野广智,孟庆勇,张培华等. 增生性疤痕组织与正常上皮组织 FTIR 光谱研究.光谱学与光谱分析,2003,23(2):270-273
    [246] 凌晓锋, 徐智, 徐怡庄等. 傅里叶变换红外光谱应用于乳腺癌临床诊断探索. 光谱学与光谱分析. 2005,25(2):198-201
    [247] Wolkers WF, Bochicchio A, Selvaggi G, et al. Fourier transform infrared microspectroscopy detects changes in protein secondary structure associated with desiccation tolerance in developing maize embryos. Plant Physiol. 1998, 116: 1169-1177
    [248] Oldenhof H, Wolkers WF, Bowman JL, et al. Freezing and desiccation tolerance in the moss Physcomitrella patens: An in situ Fourier transform infrared spectroscopic study. Biochimica et Biophysica Acta. 2006, 1760:1226-1234
    [249] Mittler R. Oxidative stress, antioxidants and stress tolerance. Trends Plant Sci. 2002, 7: 405–410
    [250] Tsvetkova NM, Horváth I, T?r?k Z, et al. Small heat-shock proteins regulate membrane lipid polymorphism. Proc. Natl. Acad. Sci. USA. 2002, 99: 13504-13509
    [251] Hincha DK, Zuther E, Heyer AG. The preservation of liposomes by raffinose family oligosaccharides during drying is mediated by effects on fusion and lipid phase transitions. Biochimica et Biophysica Acta. 2003, 1612: 172–177
    [252] Haris PI, Coke M, Chapman D. Fourier transform infrared spectroscopic investigation of rhodopsin structure and its comparison with bacteriorhodopsin. Biochim. Biophys. Acta. 1989, 995: 160–167
    [253] Wolkers WF, Hoekstra FA. In situ FTIR assessment of desiccation-tolerant tissues, Spectroscopy. 2003, 17:297–313
    [254] Richardson DHS. The Biology of Mosses. Blackwell Scientific Publications, London. 1981
    [255] N?rr M. Hitzeresistenz bei Moosen. Flora. 1974, 163: 388–397
    [256] Kappan L. Ecological significance of resistance to high temperature. In Lange OL, Nobel PS, Osmond CB, Ziegler H eds(Encyclopedia of Plant Physiology 12A, Physiological Plant Ecology I). Springer, NY. 1981: 439–474
    [257] Meyer H, Santarius KA. Short-term thermal acclimation and heat tolerance of gametophytes of mosses. Oecologia. 1998, 115: 1–8
    [258] T?r?k Z, Tsvetkova NM, Balogh G, et al. Heat shock protein coinducers with no effect on protein denaturation specifically modulate the membrane lipid phase. Proc. Natl. Acad. Sci. USA. 2003, 100: 3131-3136
    [259] Shepherd T, Griffiths DW. The effects of stress on plant cuticular waxes. New Phytologist. 2006, 171:469-499
    [260] Los DA, Murata N. Structure and expression of fatty acid desaturases. Biochim Biophys Acta. 1998, 1394:3–15
    [261] Saito T, Kato A, Ochiai H, et al. Temperature adaptation in Dictyostelium: role of Δ5 fatty acid desaturase. Microbiology. 2005, 151:113-119
    [262] Vigh L, Escribá PV, Sonnleitner A, et al. The significance of lipid composition for membrane activity: New concepts and ways of assessing function. Progress in Lipid Research. 2005, 44: 303–344
    [263] Trent JD, Kagawa HK, Paavola CD, et al. Intracellular localization of a group II chaperonin indicates a membrane-related function. Proc. Natl. Acad. Sci. USA. 2003, 100: 15589 – 15594
    [264] Buzzard KA, Giaccia AJ, Killender M, et al. Heat shock protein 72 modulates pathways of stress-induced Apoptosis. J Biol. Chem. 1998, 273:17147- 17153
    [265] Hartl FU, Martin J, Neupert A. Protein Folding in the Cell: The Role of Molecular Chaperones Hsp70 and Hsp60. Annual Review of Biophysics and Biomolecular Structure. 1992, 21: 293-322
    [266] Park SY, Shivaji R, Krans JV, et al. Heat-shock response in heat-tolerant and nontolerant variants of Agrostis palustris Huds. Plant Physiol. 1996, 111:515–524
    [267] Malik MK, Slovin JP, Hwang CH, et al. Modified ex-pression of a carrot smallheat shock protein gene, hsp17.7, results in increased or decreased thermotolerance. Plant J. 1999, 20: 89–99
    [268] Sanchez Y, Taulien J, Borkovich KA, et al. Hsp104 is required for thermotolerance to many forms of stress. EMBO J. 1992, 11:2357–2364
    [269] Gurley WB. HSP101: A key component for the acquisition of thermotolerance in plants. Plant Cell. 2000, 12: 457-460
    [270] Oliver MJ, Dowd SE, Zaragoza J, et al. The rehydration transcriptome of the desiccation-tolerant bryophyte Tortula ruralis: transcript classification and analysis. BMC Genomics. 2004, 5:89
    [271] Becquerel P. La suspension de la vie des spores des algues, lichens, et mousses aux confins du zéro absolue et role dela synérèse réversible pour leur survie au dégel expliquant l’existence de la flore polaire et des hautes altitudes. C.R. Acad. Sci. Paris. 1951, 232:22–25.
    [272] Bewley, JD. Desiccation and protein synthesis in the moss Tortula ruralis. Can. J.Bot. 1973, 51:203–206.
    [273] Burke MJ. The glass state and survival of anhydrous biological systems. In:Leopold AC ed(Membranes,Metabolism and Dry Organism). New York: Cornell University Press. 1986:358~364
    [274] Y. Roos, K. Jouppila and B. Zielasko, Non-enzymatic browning-induced water plastification. Glass transition temperature depression and reaction kinetics determination using DSC. Journal of Thermal Analysis. 1996, 47: 1437–1450.
    [275] Hancock B, Zografi G. Characteristics and significance of the amorphous state in pharmaceutical systems. Journal of Pharmaceutical Sciences. 1997, 86: 1–12
    [276] Leopold AC, Sun WQ, Bernal-Lugo I. The glassy state in seeds: analysis and function. Seed Sci. Res. 1994, 4:267-274
    [277] Crowe JH, Carpenter JF, Crowe LM. The role of vitrification in anhydrobiosis. Annual Review of Physiology. 1998, 60: 73–103
    [278] Chang BS, Beauvais RM, Dong A, et al. Physical factors affecting the storage stability of freeze-dried interleukin-1 receptor antagonist: glass transition and protein conformation. Arch Biochem Biophys. 1996, 331:249-258
    [279] Sun WQ, Leopold AC, Crowe LM, et al. Stability of dry liposomes in sugar glasses. Biophysical Journal. 1996, 70: 1769–1776
    [280] Roos Y, Karel M. Phase transitions of mixtures of amorphous polysaccharides and sugars. Biotechnology Progress. 1991, 7: 49–53
    [281] Leprince O, Walters-Vertucci CA. Calorimetric study of glass transition behaviors in axes of bean with relevance to storage stability. Plant Physiol. 1995, 109:1471–1481
    [282] Buitink J, Walters-Vertucci C, Hoekstra FA, et al. Calorimetric properties of dehydrating pollen. Plant Physiol. 1996, 111:235–242
    [283] Ghasempour, HR, Gaff DF, Williams RPW, et al. Contents of sugars in leaves of drying desiccation tolerant flowering plants, particularly grasses. Plant Growth Reg. 1998, 24:185-191
    [284] Slade L, Levine H. Beyond water activity: recent advances based on an alternative approach to the assessment of food quality and safety. Crit. Rev. Food Sci. Nutr. 1991, 30:115-360
    [285] Leslie SB, Israeli E, Lighthart B, et al. Trehaolose and sucrose protect both membranes and proteins in intact bacteria during drying. App Environ Microbiol. 1995, 61:3592 -3597
    [286] Crowe, LM, Reid DS, Crowe JH. Is trehalose special for preserving dry biomaterials? Biophys. J. 1996, 71:2087-2093
    [287] Buitink J, Hoekstra FA, Leprince O. Biochemistry and biophysics of tolerance systems. In M. Black and H. W. Pritchard (eds.) (Desiccation and survival of plants: Drying without dying). CAB International, Wallingford. 2002: 293–318.
    [288] Rowe ES, Zhang F, Leung TW, et al. Thermodynamics of membrane partitioning for a series of n-alcohols determined by titration calorimetry: role of hydrophobic effects. Biochemistry. 1998, 37: 2430-2440
    [289] Mazzanti L, Curatola G, Zolese G, et al. Lipid–protein interactions in mitochondria. VIII. Effect of general anesthetics on the mobility of spin labels in lipid vesicles and mitochondrial membranes. J. Bioenerg. Biomembr. 1979, 11: 17–32
    [290] Franks NP, Lieb WR. Molecular and cellular mechanisms of general anaesthesia. Nature. 1994, 367: 607–614
    [291] Yokono S, Ogli K, Miura S, et al. 400 MHz two-dimensional nuclear Overhauser spectroscopy on anesthetic interaction with lipid bilayer. Biochim. Biophys. Acta 1989, 982: 300–302
    [292] Vigh L, Maresca B, Harwood JL. Does the membrane's physical state control the expression of heat shock and other genes? Trends Biochem. Sci. 1998, 23: 369–374
    [293] van der Heide T, Poolman B. Glycine Betaine Transport in Lactococcus lactis Is Osmotically Regulated at the Level of Expression and Translocation Activity. J. Bacteriol. 2000,182: 203-206
    [294] Janoff AS, Pringle MJ, Miller KW. Correlation of general anaesthetic potency with solubility in membranes. Biochimica et Biophysica Acta. 1981, 649: 125–128
    [295] Go ML, Ngiam TL. Thermodynamics of partitioning of the antimalarial drugmefloquine in phospholipid bilayers and bulk solvents. Chem. Pharmacol. Bull. 1997, 45: 2055-2060
    [296] Ultee A, Kets EPW, Smid EJ. Mechanisms of action of carvacrol on the foodborne pathogen Bacillus cereus. Appl. Environ. Microbiol. 1999, 65: 4606-4610
    [297] Golovina EA, Hoekstra FA, Hemminga MA. Drying increases intracellular partitioning of amphiphilic substances into the lipid phase: impact on membrane permeability and significance for desiccation tolerance. Plant Physiol. 1998, 118: 975–986
    [298] Hoekstra FA, Golovina EA, Van Aelst AC, et al. Imbibitional leakage from anhydrobiotes revisited. Plant Cell Environ. 1999, 22: 1121-1131
    [299] Hoekstra FA, Golovina EA. Impact of amphiphile partitioning on desiccation tolerance. In: M. Black, K.J. Bradford and J. Vasques-Ramos (eds) (Seed Biology: Advances and Applications). CAB International: Wallingford. 2000: 43–55
    [300] Marsh D. Electron spin resonance: spin labels. In E Grell (eds) (Membrane Spectroscopy: Molecular Biology, Biochemistry and Biophysics) Vol. 31. Springer-Verla: Berlin. 1981: 51-142
    [301] Sankaram, M. B., and Marsh, D. (1993) Protein-lipid interactions with peripheral membrane proteins. In: New Comprehensive Biochemistry, Vol. 25. Protein-Lipid Interactions (Watts, A., ed.). Elsevier, Amsterdam, pp. 127-162.
    [302] Golovina EA, Tikhonov AN. The structural differences between the embryos of viable and nonviable wheat seeds as studied with the EPR spectroscopy of lipid-soluble spin labels. Biochim. Biophys. Acta. 1994, 1190: 385–392
    [303] Golovina EA, Hoekstra FA, van Aelst AC. The competence to acquire cellular desiccation tolerance is not dependent on seed morphological development. J. Exp. Bot. 2001, 52: 1015–1027
    [304] Riezman, H. Why do cells require heat shock proteins to survive heat stress? Cell Cycle. 2004, 3: 61–63
    [305] Keith AD, Snipes W. Viscosity of cellular protoplasm. Science. 1974, 183, 666–668
    [306] Buitink J, Claessens MMAE, Hemminga MA, et al. Influence of water content and temperature on molecular mobility and intracellular glasses in seeds and pollen. Plant Physiol. 1998, 118: 531-541
    [307] Leprince O, Hoekstra FA. The response of cytochrome redox state and energy metabolism to dehydration support a role for cytoplasmic viscosity in desiccation tolerance. Plant Physiol. 1998, 118: 1253-1264
    [308] Spooner PJR, Friesen RHE, Knol J, et al. Rotational mobility and orientationalstability of a transport protein in lipid membranes. Biophy. J. 2000, 79: 756-766.
    [309] Sun WQ, Leopold AC. Cytoplasmic vitrification and survival of anhydrobiotic organisms. Comp. Biochem. Physiol. 1997, 117A:327-333
    [310] Tieleman DP, Marrink SJ, Berendsen HJC. A computer perspective of membranes: molecular dynamics studies of lipid bilayer systems. Biochimica et Biophysica Acta. 1997, 1331: 235–270
    [311] Bales BL, Leon V. Magnetic resonance studies of eukaryotic cells. III. Spin labeled fatty acids in the plasma membrane. Biochimica et Biophysica Acta. 1978, 509: 90–99.
    [312] Leopold AC. Temperature effects on soybean imbibition and leakage. Plant Physiol. 1980, 65: 1096-1098
    [313] Becwar MR, Stanwood PC, Roos EE. Dehydration effects on imbibitional leakage from desiccation-sensitive seeds. Plant physiology. 1982, 69:1132-1135
    [314] Leopold AC, Musgrave ME, Williams KM. Solute leakage resulting from leaf desiccation. Plant Physiol. 1981, 68: 1222–1225.
    [315] Miller RJ, Koeppe DE. The effect of calcium and inhibitors on corn mitochondrial respiration. Plant Physiol. 1971, 47: 832–835
    [316] Conlon T, Outhred R. Water diffusion permeability of erythrocytes using an NMR technique. Biochim. Biophys. Acta. 1972, 288: 354-361
    [317] Baci? G, Ratkovi? S. Water exchange in plant tissue studied by proton NMR in the presence of paramagnetic centers. Biophys J. 1984, 45(4): 767–776
    [318] Ishida N, Koizumi M, Kano H. Location of sugars in barley seeds during germination by NMR microscopy. Plant Cell Environ. 1996, 19:1415–1422
    [319] Fleischer G., Werner A. Study of water and oil diffusion in rape seeds with sorption-desorption and NMR-techniques. Biochim. et Biophys. Acta. 1992, 1116: 305-308
    [320] Leprince O, Harren FJM, Buitink J, et al. Metabolic dysfunction and unabated respiration precede the loss of membrane integrity during dehydration of germinating radicles. Plant Physiol. 2000,122: 597-608
    [321] Boss WF, Moot RL. Effects of divalent cations and polyethylene glycol on the membrane fluidity of protoplast. Plant Physiol. 1980, 66: 835-837
    [322] Je?ek P, Bauer M, Trommer WE. EPR spectroscopy of 5-DOXYL-stearic acid bound to the mitochondrial uncoupling protein reveals its competitive displacement by alkylsulfonates in the channel and allosteric displacement by ATP. FEBS Lett. 1995, 361: 303-307
    [323] da Silveira MG, Golovina EA, Hoekstra FA, et al. Membrane fluidity adjustmentsin ethanol-stressed Oenococcus oeni cells. Appl. Environ. Microbiol. 2003, 69: 5826–5832
    [324] Tucker EB,Bewley JD. Plant desiccation and protein systhesis. Ш. Stability of cytoplasmic RNA during dehydration and its synthesis on rehydration of the moss Tortula ruralis. Plant Physiol. 1976, 57: 564-567
    [325] Oliver MJ,Bewley JD. Plant desiccation and protein synthesis. ?V. RNA synthesis, stability, and recruitment of tolerant moss Tortula ruralis. Plant Physiol. 1984b, 74:21-25
    [326] Oliver MJ,Bewley JD. Plant desiccation and protein synthesis. V. Stability of poly(A)+ RNA during desiccation and their synthesis upon rehydration in the desiccation-tolerant moss Tortula ruralis and the intolerant moss Crateneuron filicinum. Plant Physiol. 1984c, 74: 917-922
    [327] BernacchiaG, Salamini F, Bartels D. Molecular characterization of the rehydration process in the resurrection plant Craterostigma plantagineum. Plant Physiol. 1996, 111:1043-1050
    [328] Boudet J, Buitink J, Hoekstra FA, et al. Comparative analysis of the heat stable proteome of radicles of Medicago truncatula seeds during germination indentifies Late Embryogenesis Abundant proteins associated with desiccation tolerance. Plant Physiol. 2006, 140:1418-1436
    [329] Ingle RA, Schmidt UG, Farrant JM, et al. Proteomic analysis of leaf proteins during dehydration of the resurrection plant Xerophyta viscose. Plant, Cell and Environment. 2007,30: 435-446
    [330] Sarnighausen E, Wurtz V, Heintz D, et al. Mapping of the Physcomitrella patens proteome. Phytochemistry. 2004, 65: 1589-1607
    [331] Oliver MJ. Influence of protoplasmic water loss on the control of protein synthesis in the desiccation-tolerant moss Tortula ruralis. Plant Physiol.1991, 97: 1501-1511
    [332] Gallardo K, Job C, Groot SPC, et al. Proteomic analysis of Arabidopsis seed germination and priming. Plant Physiol. 2001, 126: 835-848
    [333] Finnie C, Maeda K, ?stergaard O, et al. Aspects of the barley seed proteome during development and germination. Biochemical Society Transactions. 2004, 34: 517-519
    [334] 翟大勇,沈黎明. 脱水蛋白研究进展[J].生物化学与生物物理学进展.1998,25(2): 119- 122
    [335] Allagulova CR, Gimalov FR, Shakirova FM, et al. The plant dehydrins: structure and putative functions. Biochemistry. 2003, 68: 945-951
    [336] Danyluk J, Perron A, Houde M, et al. A accumulation of an acidic dehydrin in the vicinity of the plasma membrane during cold acclimation of wheat. Plant cell. 1998, 10: 623-638.
    [337] 李晶,阎秀峰,祖元刚等. 低温胁迫下红松幼苗活性氧产生及保护酶变化.植物学报. 2000,42(2):148-152
    [338] 黄清泉,孙歆,张年辉等. 水杨酸对水分胁迫黄瓜幼苗叶片生理过程影响. 西北植物学报. 2004,24(12): 2202-2207
    [339] Hara M, Fujinaga M, Kuboi T. Radical scavenging activity and oxidative modification of citrus Dehydrin. Plant Physiol. Biochem. 2004, 42: 657-662
    [340] Scott HBΠ, Oliver MJ. Accumulation and polysomal recruitment of transcripts in response to desiccation and rehydration of the moss Tortula ruralis. J. Exp. Bot. 1994, 45: 577-583
    [341] HightowerL, Nover L. Heat shock and development. Berlin: Springer-Verlag. 1991
    [342] Gerogopoulos C, Welch WJ. Role of the major heat shock proteins as molecular chaperones. Annu. Rev. Cell Biol.1993,9: 601-634
    [343] Hendrick JP, Hartl FU. Molecular chaperone functions of heat-shock proteins. Annu.Rev.Biochem. 1993,62: 349-384
    [344] Gerner EW, Scheider MJ. Induced thermal resistance in Hela cell. Nature.1975, 256: 500-502
    [345] Nagao RT, Klmpel JA, Vierling E, et al. The heat shock response: A comparative analysis. In Oxford surveys of Plant Molecular and Cell Biology, Vol.3 Miflin BJ ed (London: Oxford University Press). 1986: 384-438
    [346] Lindquist S, Craig EA. The heat-shock proteins. Annu. Rev. Genet.1988, 22: 631-677
    [347] Waters ER, Lee GJ, Vierking E. Evolution, structure and function of the small heat shock proteins in plants. J Exp. Bot. 1996, 47: 325-338
    [348] Gaestel M, Vierling E, Buchner J. The small heat shock protein (sHsp) family: an overview. In Gething MJ ed (Guide book to Molecular Chaperones and Protein-Folding Catalysis).Oxford University Press, New York. 1997: 269-272
    [349] Lee GJ, Vierling E. A small heat shock protein cooperates with heat shock protein70systems to reactivate a heat-denatured protein. Plant Physiol. 2000, 122: 189-197
    [350] Gaff D. Responses of desiccation-tolerant ‘resurrection’ plant to water stress. In Krebb PJ ed (Structure and functional responses to environmental stresses). SPBAcademic Publishers, the Hague the Netherland. 1989: 256-268
    [351] Bewley JD, Oliver MJ. Desiccation-tolerance in vegetative plant tissues and seeds: protein systhesis in relation to desiccation and a potential role for protection and repair mechanisms. In Osmond CB ed (Plant responses to cellular dehydration during environmental stress). Current Topics in Plant Physiology: American Society Plant Physiology, Series Vol 10. 1992: 141-160
    [352] Proctor MCF, Nagy Z, Csintalan Z, et al. Water-content components in bryophytes: analysis of pressure-volume relationships. J.Exp.Bot.1998,49: 1845-1854
    [353] Bohnert H. What makes desiccation tolerable? Genome Biology. 2000, ?(2): 1-4