温度和光照强度对鼠尾藻生长和生化组成的影响

在实验室条件下,研究了温度(10、15、20、25 ℃)和光照强度(20、60、100、140、180 μE·m^-2·s^-1)对鼠尾藻生长和生化组成的影响.结果表明,温度、光照强度及两者的交互作用对鼠尾藻生长均具有极显著影响.鼠尾藻在15 ℃和20 ℃下生长速率较高,随着温度的升高,达到最大生长速率所需要的光照强度有上升趋势.在10 ℃和15 ℃下,较高的光照强度对鼠尾藻生长产生了一定抑制作用,而在20 ℃和25 ℃下,其生长速率总体随光照强度的增加而增加.温度和光照强度对鼠尾藻叶绿素a、墨角藻黄素的含量影响极显著,其中光照强度的影响大于温度.总体上,叶绿素a和墨角藻黄素的含量均随着光照强度的升高而显著下降,随着温度的升高而升高.鼠尾藻碳水化合物含量随着光照强度的升高而显著升高,而温度对碳水化合物含量影响不显著.鼠尾藻蛋白质含量随着光照强度的增加而显著下降,在10 ℃和15 ℃下含量较高,随着温度的继续升高,蛋白质含量呈下降趋势.光照强度和温度的变化可改变鼠尾藻的藻体成分含量,这种改变可能是鼠尾藻为了适应环境因子改变而做出的积极的生理调节,对其生长和生存具有重要的生态意义.     

不同含水量大葱种子贮藏过程中的糖代谢研究

将大葱种子干燥到1．8％～10．5％的不同含水量后,在50℃、35℃、20℃和-18℃条件下密闭贮存16个月。通过对半乳糖、葡萄糖、果糖、蔗糖和密三糖含量研究的结果表明,随着贮存温度的升高,种子中半乳糖的含量不断升高,随着含水量的降低,种子中半乳糖的含量逐渐降低,且随着贮存温度的下降,种子中半乳糖含量随种子含水量下降而降低的趋势减缓。然而葡萄糖、果糖、蔗糖和密三糖的结果与半乳糖的变化趋势相反,随着贮存温度的升高,4种糖的含量逐渐下降,在同一贮藏温度条件下,随含水量的降低这4种糖的含量却逐渐升高,但在贮存温度较低时（20℃和～18℃）,这种变化趋势不明显。     

Effects of different temperatures and density on the survival and reproduction of Aphis gossypii on cotton plants

为探索趋近自然状态的渐变性高温胁迫对不同密度棉蚜Aphis gossypii Glover的影响,室内研究了4种不同高温模式下,不同密度(5、10、20、40)棉蚜的存活和繁殖.结果表明:随着最高温度值的升高和密度的增加,棉蚜存活率和繁殖率均呈下降趋势.当最高温度值升至40℃以上时,棉蚜存活率和繁殖率均显著下降,不同密度棉蚜存活率和繁殖率均没有差异.即随着温度的升高,密度对棉蚜的作用逐渐减弱.最高温度值为42℃时,棉蚜在3～4d内全部死亡.研究结果为提高棉蚜种群预测准确性、科学决策防治措施提供依据.     

马占相思树苗对低温冻害的抗性研究

以盆栽马占相思PNG17868家系树苗为材料,研究了低温胁迫下树苗生长发育有关的生理生化指标的变化及其抗冻害的关系。结果表明:随着低温胁迫程度的加深和时间延长,植株细胞电导率显著升高,细胞膜ATPase活性呈下降趋势,而可溶性糖、脯氨酸和可溶性蛋白质含量亦不断升高,表现出耐寒植物较典型的生理特点,说明该植物有明显的渗透调节能力和抗寒性。在零下低温(0～6℃)胁迫下,植物细胞防御系统的保护酶类(CAT、POD、SOD)的活性先是升高,然后有所下降,但下降幅度不大。这表明了马占相思PNG17868家系对低温有较强的适应能力,在温度日益降低(0～6℃)条件下体内保护酶仍能维持较高的活性水平,减轻了由膜脂过氧化引起的膜伤害,是植物提高抗寒性、免遭低温冻害的重要原因。     

底泥中微囊藻复苏和生长特性的研究

研究了微囊藻群体从底泥中释放进入水体的过程及这一过程与水体温度、光照及营养盐的关系 ,并比较了底泥和水体中微囊藻群体的生长特性。同时 ,比较了温度对经低温 (4℃ )处理的和处于对数期的Microcystis.sp .94 0的叶绿素荧光强度的影响。结果表明 ,在 15℃ ,30 μEm-2 s-1光照条件下 ,底泥中的微囊藻群体复苏开始启动 ,并于15d后开始上升到水体中。研究表明 ,存在于底泥中的微囊藻群体从底泥中迁移至上层水体的最适条件为 2 0℃ ,30 μEm-2 s-1。分别培养底泥微囊藻群体和同时期水体中的微囊藻群体 ,研究它们的生长特性 ,发现底泥中的微囊藻群体生长的最适温度为 2 0℃ ,光照强度为 30 μEm-2 s-1,与同期水体中的微囊藻群体生长条件相似。经低温 (4℃ )处理的微囊藻群体和生长周期处于对数期的微囊藻群体叶绿素荧光的影响的实验中 ,作者发现在 2 0℃和 2 5℃时 ,两种经过不同处理的微囊藻群体都随着时间增加而增长。但是 ,在 10℃和 15℃时 ,低温处理的微囊藻群体的叶绿素荧光随着时间增加而增长 ,而处于对数期的微囊藻群体的叶绿素荧光随着时间增加而降低。这表明长期处于低温和黑暗环境中的微囊藻细胞的光系统Ⅱ未受到严重的损伤 ,当环境转变有利于生长时 ,微囊藻细胞的光系统Ⅱ恢复活性。本研究结     

不同的高温模式对不同密度棉蚜存活和繁殖的影响

为探索趋近自然状态的渐变性高温胁迫对不同密度棉蚜Aphis gossypii Glover的影响,室内研究了4种不同高温模式下,不同密度(5、10、20、40)棉蚜的存活和繁殖。结果表明:随着最高温度值的升高和密度的增加,棉蚜存活率和繁殖率均呈下降趋势。当最高温度值升至40℃以上时,棉蚜存活率和繁殖率均显著下降,不同密度棉蚜存活率和繁殖率均没有差异。即随着温度的升高,密度对棉蚜的作用逐渐减弱。最高温度值为42℃时,棉蚜在3～4 d内全部死亡。研究结果为提高棉蚜种群预测准确性、科学决策防治措施提供依据。     

DPH标记法研究杀虫剂对二化螟线粒体膜流动性的影响

以DPH为荧光探剂,采用荧光偏振法研究了几种常用农药对二化螟Chilo supperssalis(Walekr)线粒体膜流动性的影响。结果表明,DPH是一种有效的荧光探剂,可以用来研究线粒体膜脂的流动性。不同种类的农药对二化螟线粒体膜的流动性都有一定的影响,但是以三氟氯氰菊酯、高效氯氰菊酯和硫丹影响较大,甲胺磷、三唑磷和克百威影响较小。三氟氯氰菊酯和高效氯氰菊酯可使膜的流动性下降,而硫丹、甲胺磷、三唑磷和克百威则使膜的流动性增强。对膜影响较大的三氟氯氰菊酯和硫丹对膜流动性的影响,还存在一定的剂量-效应关系。另外,膜的流动性受温度的影响很大,在温度分别为17、27、37℃的条件下,在药剂浓度为1×10-4mol/L时,甲胺磷在3个温度下对膜的流动性影响都很小,在误差范围内几乎没有影响;硫丹不同温度下都使膜的流动性增强,而三氟氯氰菊酯则使膜的流动性降低。     

干热处理对甜瓜种子活力和细菌性果斑病抑制能力的影响

以厚皮甜瓜品种‘哈密绿’种子为材料,在70℃、75℃和80℃温度下分别处理24h、48h和72h,研究不同干热处理对甜瓜种子活力萌发和生理生化指标变化及细菌性果斑病的防治效果。结果显示:(1)随着处理温度的升高和时间的延长,干热处理甜瓜种子发芽指标和成苗率显著下降,而70℃处理24h和48h对种子发芽指标(活力指数除外)和成苗率无显著影响。(2)与对照相比,干热处理种子胚芽中的SOD活性、可溶性糖和脯氨酸含量升高,在同一温度处理下,SOD活性和可溶性糖含量随着处理时间的延长基本呈增长趋势,脯氨酸含量则随着处理时间的延长呈下降趋势,POD和APX活性以及可溶性蛋白含量变化随着温度的升高和处理时间的延长呈下降趋势;与对照相比,胚芽中CAT活性在70℃处理下降低,而在75℃和80℃处理下升高,但其随着处理时间的延长呈下降趋势;胚芽中O-·2产生速率在70℃和75℃处理下与对照接近,而在80℃处理下随着处理时间的延长呈上升趋势,且均显著高于对照。(3)随着处理温度的升高和时间的延长,甜瓜接菌种子幼苗细菌性果斑病发病率较对照显著降低。研究表明,适宜干热处理温度和时间诱导甜瓜种子中抗氧化酶活性增强,渗透调节物质含量增加,超氧阴离子产生速率降低,种子活力和出苗率有效提高,‘哈密绿’种子有效、安全的干热处理组合为70℃、48h。     

外源水溶性有机物及温度对红壤铜形态的影响

利用模拟培养试验研究了外源水溶性有机物（DOM）添加量和培养温度对红壤中Cu形态的影响. 结果表明: 与不添加DOM比较, 添加不同量的DOM均可提高土壤中交换态Cu的含量、降低铁锰结合态Cu含量; 随着培养时间的延长,不同DOM添加量下土壤交换态Cu含量呈逐渐下降趋势;至试验结束时,DOM添加量为250 mg·L^-1时土壤交换态和碳酸盐结合态Cu含量最高, 添加量为500 mg·L^-1时铁锰结合态Cu含量最高;不同DOM添加量下, 土壤中有机结合态Cu含量较CK增加10.67%～23.66%. 在25 ℃和45 ℃温度条件下, 添加DOM后土壤交换态和铁锰结合态Cu含量均随培养时间的延长呈下降趋势, 但在5 ℃下变化趋势相反; 3种温度下添加DOM后土壤碳酸盐结合态Cu含量有随培养时间延长而增加的趋势. 随着培养温度的升高,土壤有机结合态Cu含量增加, 但在温度较低(5 ℃)时土壤残渣态Cu含量下降.     

长白山阔叶红松林CO2通量与温度的关系

应用涡度相关法观测的通量数据和环境因子数据,在生态系统水平上分析了长白山阔叶红松林生长季温度与CO2通量之间的关系.结果表明：（1）在相同的光合有效辐射水平下,净生态系统CO2交换量（NEE）随温度Ta的变化趋势为,在Ta〈20℃范围内,NEE随温度的增加而增加,在Ta=20℃附近有极大值,随温度的继续增加NEE呈下降的趋势,同时NEE还具有明显的季节变化,表现为7月〉6月〉8月〉9月〉5月〉4月〉10月.（2）应用Michaelis-Menten方程计算得出最大光合速率Pmax和生态系统呼吸Re,分析其与温度的关系发现,Pmax随温度的变化呈S型曲线,Re则随着温度的升高而呈指数上升的趋势,曲线为：Re=0.0607 exp（0.0666Tα）,R^2=0.96.夜间生态系统呼吸的Q10为3.15.（3）通过对NEE与环境因子的偏相关分析表明,温度对NEE的偏相关系数在生长季呈现先减小后增大的趋势,说明在生长季初期和末期升高温度比生长季中期对NEE的影响要大.     

Role of membrane fluidity in pressure resistance of Escherichia coli NCTC 8164

The relationship among growth temperature, membrane fatty acid composition, and pressure resistance was examined in Escherichia coli NCTC 8164. The pressure resistance of exponential-phase cells was maximal in cells grown at 10 degrees C and decreased with increasing growth temperatures up to 45 degrees C. By contrast, the pressure resistance of stationary-phase cells was lowest in cells grown at 10 degrees C and increased with increasing growth temperature, reaching a maximum at 30 to 37 degrees C before decreasing at 45 degrees C. The proportion of unsaturated fatty acids in the membrane lipids decreased with increasing growth temperature in both exponential- and stationary-phase cells and correlated closely with the melting point of the phospholipids extracted from whole cells examined by differential scanning calorimetry. Therefore, in exponential-phase cells, pressure resistance increased with greater membrane fluidity, whereas in stationary-phase cells, there was apparently no simple relationship between membrane fluidity and pressure resistance. When exponential-phase or stationary-phase cells were pressure treated at different temperatures, resistance in both cell types increased with increasing temperatures of pressurization (between 10 and 30 degrees C). Based on the above observations, we propose that membrane fluidity affects the pressure resistance of exponential- and stationary-phase cells in a similar way, but it is the dominant factor in exponential-phase cells whereas in stationary-phase cells, its effects are superimposed on a separate but larger effect of the physiological stationary-phase response that is itself temperature dependent.     

Relationship between membrane damage and cell death in pressure-treated Escherichia coli cells: differences between exponential- and stationary-phase cells and variation among strains

The relationship between membrane damage and loss of viability following pressure treatment was examined in Escherichia coli strains C9490, H1071, and NCTC 8003. These strains showed high, medium, and low resistance to pressure, respectively, in stationary phase but similar resistance to pressure in exponential phase. Loss of membrane integrity was measured as loss of osmotic responsiveness or as increased uptake of the fluorescent dye propidium iodide. In exponential-phase cells, loss of viability was correlated with a permanent loss of membrane integrity in all strains, whereas in stationary-phase cells, a more complicated picture emerged in which cell membranes became leaky during pressure treatment but resealed to a greater or lesser extent following decompression. Strain H1071 displayed a very unusual pressure response in stationary phase in which survival decreased to a minimum at 300 MPa but then increased at 400 to 500 MPa before decreasing again. Membranes were unable to reseal after treatment at 300 MPa but could do so after treatment at higher pressures. Membrane damage in this strain was thus typical of exponential-phase cells under low-pressure conditions but of stationary-phase cells under higher-pressure conditions. Heat shock treatment of strain H1071 cells increased pressure resistance under low-pressure conditions and also allowed membrane damage to reseal. Growth in the presence of IPTG (isopropyl-beta-D-thiogalactopyranoside) increased resistance under high-pressure conditions. The mechanisms of inactivation may thus differ at high and low pressures. These studies support the view that membrane damage is an important event in the inactivation of bacteria by high pressure, but the nature of membrane damage and its relation to cell death may differ between species and phases of growth.     

Morphological and Physiological Changes Induced by High Hydrostatic Pressure in Exponential- and Stationary-Phase Cells of Escherichia coli: Relationship with Cell Death

The relationship between a loss of viability and several morphological and physiological changes was examined with Escherichia coli strain J1 subjected to high-pressure treatment. The pressure resistance of stationary-phase cells was much higher than that of exponential-phase cells, but in both types of cell, aggregation of cytoplasmic proteins and condensation of the nucleoid occurred after treatment at 200 MPa for 8 min. Although gross changes were detected in these cellular structures, they were not related to cell death, at least for stationary-phase cells. In addition to these events, exponential-phase cells showed changes in their cell envelopes that were not seen for stationary-phase cells, namely physical perturbations of the cell envelope structure, a loss of osmotic responsiveness, and a loss of protein and RNA to the extracellular medium. Based on these observations, we propose that exponential-phase cells are inactivated under high pressure by irreversible damage to the cell membrane. In contrast, stationary-phase cells have a cytoplasmic membrane that is robust enough to withstand pressurization up to very intense treatments. The retention of an intact membrane appears to allow the stationary-phase cell to repair gross changes in other cellular structures and to remain viable at pressures that are lethal to exponential-phase cells.     

Morphological and physiological changes induced by high hydrostatic pressure in exponential- and stationary-phase cells of Escherichia coli: relationship with cell death

The relationship between a loss of viability and several morphological and physiological changes was examined with Escherichia coli strain J1 subjected to high-pressure treatment. The pressure resistance of stationary-phase cells was much higher than that of exponential-phase cells, but in both types of cell, aggregation of cytoplasmic proteins and condensation of the nucleoid occurred after treatment at 200 MPa for 8 min. Although gross changes were detected in these cellular structures, they were not related to cell death, at least for stationary-phase cells. In addition to these events, exponential-phase cells showed changes in their cell envelopes that were not seen for stationary-phase cells, namely physical perturbations of the cell envelope structure, a loss of osmotic responsiveness, and a loss of protein and RNA to the extracellular medium. Based on these observations, we propose that exponential-phase cells are inactivated under high pressure by irreversible damage to the cell membrane. In contrast, stationary-phase cells have a cytoplasmic membrane that is robust enough to withstand pressurization up to very intense treatments. The retention of an intact membrane appears to allow the stationary-phase cell to repair gross changes in other cellular structures and to remain viable at pressures that are lethal to exponential-phase cells.     

Evidence for a correlation between swimming velocity and membrane fluidity of Tetrahymena cells

The influence of the physical state of the membrane on the swimming behaviour of Tetrahymena pyriformis was studied in cells with lipid-modified membranes. When the growth temperature of Tetrahymena cells was increased from 15 degrees C to 34 degrees C or decreased from 39 degrees C to 15 degrees C, their swimming velocity changed gradually in a similar to the adaptive change in membrane lipid composition. Therefore, such adaptive changes in swimming velocity were not observed during short exposures to a different environment. Tetrahymena cells adapted to 34 degrees C swam at 570 microns/s. On incubation at 15 degrees C these cells swam at 100 microns/s. When the temperature was increased to 34 degrees C after a 90-min incubation at 15 degrees C, the initial velocity was immediately recovered. On replacement of tetrahymanol with ergosterol, the swimming velocity of 34 degrees C-grown cells decreased to 210 microns/s, and the cells ceased to move when the temperature was decreased to 15 degrees C. To investigate the influence of the physical state of the membrane on the swimming velocity, total phospholipids were prepared from Tetrahymena cells grown under these different conditions. The fluidities of liposomes of these phospholipid were measured using stearate spin probe. The membrane fluidity of the cells cooled to 15 degrees C increased gradually during incubation at 15 degrees C. On the other hand, the fluidity of the heated cell decreased during incubation at 34 degrees C. Replacement of tetrahymanol with ergosterol decreased the membrane fluidity markedly. Consequently, a good correlation was observed between swimming velocity and membrane fluidity; as the membrane fluidity increased, the swimming velocity increased linearly up to 600 microns/s. These results provide evidence for the regulation of the swimming behaviour by physical properties of the membrane.     

Metabolic control of the membrane fluidity in Bacillus subtilis during cold adaptation

Membrane fluidity adaptation to the low growth temperature in Bacillus subtilis involves two distinct mechanisms: (1) long-term adaptation accomplished by increasing the ratio of anteiso- to iso-branched fatty acids and (2) rapid desaturation of fatty acid chains in existing phospholipids by induction of fatty acid desaturase after cold shock. In this work we studied the effect of medium composition on cold adaptation of membrane fluidity. Bacillus subtilis was cultivated at optimum (40 degrees C) and low (20 degrees C) temperatures in complex medium with glucose or in mineral medium with either glucose or glycerol. Cold adaptation was characterized by fatty acid analysis and by measuring the midpoint of phospholipid phase transition T(m) (differential scanning calorimetry) and membrane fluidity (DPH fluorescence polarization). Cells cultured and measured at 40 degrees C displayed the same membrane fluidity in all three media despite a markedly different fatty acid composition. The T(m) was surprisingly the highest in the case of a culture grown in complex medium. On the contrary, cultivation at 20 degrees C in the complex medium gave rise to the highest membrane fluidity with concomitant decrease of T(m) by 10.5 degrees C. In mineral media at 20 degrees C the corresponding changes of T(m) were almost negligible. After a temperature shift from 40 to 20 degrees C, the cultures from all three media displayed the same adaptive induction of fatty acid desaturase despite their different membrane fluidity values immediately after cold shock.     

Lipid and protein composition of membranes of Bacillus megaterium variants in the temperature range 5 to 70 degrees C.

Membranes were prepared from four temperature range variants of Bacillus megaterium: one obligate thermophile, one facultative thermophile, one mesophile, and one facultative psychrophile, covering the temperature interval between 5 and 70 degrees C. The following changes in membrane composition were apparent with increasing growth temperatures: (i) the relative amount of iso fatty acids increased and that of anteiso acids decreased, the ratio of iso acids to anteiso acids being 0.34 at 5 degrees C and 3.95 at 70 degrees C, and the pair iso/anteiso acids thus seemed to parallel the pair saturated/unsaturated acids in their ability to regulate membrane fluidity; (ii) the relative/unsaturated acids in their ability to regulate membrane fluidity; (ii) the relative amount of long-chain acids (C16 to C18) increased fivefold over that of short-chain acids (C14 and C15) between 5 and 70 degrees C; (iii) the relative amount of phosphatidylethanolamine increased, and this phospholipid accordingly dominated in the thermophilic strains, whereas diphosphatidylglycerol was predominant in the two other strains; and (iv) the ratio of micromoles of phospholipid to milligrams of membrane protein increased three-fold between 5 and 70 degrees C. Moreover, a quantitative variation in membrane proteins was evident between the different strains. Briefly, membrane phospholipids with higher melting points and packing densities appeared to be synthesized at elevated growth temperatures.     

Cultured human skin fibroblasts modify their plasma membrane lipid composition and fluidity according to growth temperature suggesting homeoviscous adaptation at hypothermic (30 degrees C) but not at hyperthermic (40 degrees C) temperatures.

Mammalian cell metabolism is responding to changes in temperature. Body temperature is regulated around 37 degrees C, but temperatures of exposed skin areas may vary between 20 degrees C and 40 degrees C for extended periods of time without apparent disturbance of adequate cellular functions. Cellular membrane functions are depending from temperatures but also from their lipid environment, which is a major component of membrane fluidity. Temperature-induced changes of membrane fluidity may be counterbalanced by adaptive modification of membrane lipids. Temperature-dependent changes of whole cell- and of purified membrane lipids and possible homeoviscous adaptation of membrane fluidity have been studied in human skin fibroblasts cultured at 30 degrees C, 37 degrees C, and 40 degrees C for ten days. Membrane anisotropy was measured by polarized fluorescence spectroscopy using TMA-DPH for superficial and DPH for deeper membrane layers. Human fibroblasts were able to adapt themselves to hypothermic temperatures (30 degrees C) by modifying the fluidity of the deeper apolar regions of the plasma membranes as reported by changes of fluorescence anisotropy due to appropriate changes of their plasma membrane lipid composition. This could not be shown for the whole cells. At 40 degrees C growth temperature, adaptive changes of the membrane lipid composition, except for some changes in fatty acid compositions, were not seen. Independent from the changes of the membrane lipid composition, the fluorescence anisotropy of the more superficial membrane layers (TMA-DPH) increased in cells growing at 30 degrees C and decreased in cells growing at 40 degrees C.     

Correlations between the thermal stability of chloroplast (thylakoid) membranes and the composition and fluidity of their polar lipids upon acclimation of the higher plant,Nerium oleander,to growth temperature

The thermal stability of excitation transfer from pigment proteins to the Photosystem II reaction center of Nerium oleander adjusts by 10 Celsius degrees when cloned plants grown at 20°C/15°C, day/night growth temperatures are shifted to 45°C/32°C growth temperature or vice versa. Concomitant with this adjustment is a decrease in the fluidity of thylakoid membrane polar lipids as determined by spin labeling. The results are consistent with the hypothesis that there is a limiting maximum fluidity compatible with maintenance of native membrane structure and function. This limiting fluidity was about the same as for a number of other species which exhibit a range of thermal stabilities. Inversely correlated shifts in lipid fluidity and thermal stability occurred during the time course of acclimation of N. oleander to new growth temperatures. Thus, the temperature at which the limiting fluidity was reached changed during acclimation while the limiting fluidity remained constant. Although the relative proportion of the major classes of membrane polar lipids remained constant during adjustments in fluidity, large changes occured in the abundance of specific fatty acids. These changes were different for the phospho- and galacto-lipids suggesting that the fatty acid composition of these two lipid classes is regulated by different mechanisms. Comparisons between membrane lipid fluidity and fatty acid composition indicate that fluidity is not a simple linear function of fatty acid composition.     

Escherichia coli membrane fluidity as detected by excimerization of dipyrenylpropane: sensitivity to the bacterial fatty acid profile.

A coordinated study of membrane fluidity and fatty acid composition has been carried out in Escherichia coli W3110. The lipid acyl chain profile of the bacteria, altered by growing cells in steady state at 30, 37, 42, or 45 degrees C, was determined by gas chromatography of the fatty acid methyl esters. In parallel experiments, total membranes obtained from cells of the above-mentioned cultures were labeled with dipyrenylpropane and their relative fluidity was measured on the basis of the excimer to monomer fluorescence intensity ratio of the fluorophore. It has been found that, at constant assay temperature, fluidity determined with dipyrenylpropane decreases gradually with the growth temperature increment, from 30 to 45 degrees C. Interestingly, when fatty acid composition is taken into account, fluidity increases linearly in the range under study, with the proportion of unsaturated fatty acyl chains, both variables being highly correlated (0.924 相似文献