两种五倍子蚜虫冬寄主藓类植物的光合特性及其与光照,温度和？…

The net photosynthesis of Thuidium cymbifolium and Chrysocladium retrorsum, two species of wintering host mosses for gullaphids, and its response to light, temperature and water content were measured with CI-301PS(CID Inc. USA) both in winter and spring. The photosynthetic capacity of Thuidium cymbifolium and Chrysocladium retrorsum was about 141 and 117 mumolCO2kg-1dw.s-1, respectively, and trended to increase from winter to spring. The light saturation point of these two mosses at 800-900 mumol.m-2.s-1 was much higher than that of many other mosses, and the compensation point ranged from 40 to 50 mumol.m-2.s-1. The temperature response curves of these two mosses were similar, with optium temperature ranging from 25 to 36 degrees C in spring, and from 20 to 30 degrees C in winter. When the temperature was below the freezing point(-15 to 0 degree C), they both maintained a distinct net photosynthesis, with the optimum water content ranging from 200 to 300(400)% dw. The photosynthesis started to be restrained evidently, when the water content declined to about 150% dw. The gas exchange ceased or became negative, when the water content was as low as 40-50% dw. It can be inferred that these two species might be both poikilothermal and poikilohydric organisms, but the resistibility of T. cymbifolium to intense light and high temperature was higher than that of C. retrorsum.     

3种藓类植物水分含量与光合作用、呼吸作用和水势的关系

对湿地匍灯藓〔Plagiomniumacutum(Lindb.)T.Kop.〕、大羽藓〔Thuidiumcymbifolium(Dozy&Molk.)Dozy&Molk.〕和垂藓〔Chrysocladiunretrorsum(Mitt.)Fleisch.〕的水分含量与光合作用、呼吸作用和水势的关系进行了初步研究（1999年5月20日到6月10日）。在这3种藓类植物中,其水分含量与光合作用速率（Pn）的关系可以分为2种类型一种类型如大羽藓和垂藓,在藓体水分含量20%～70%时,Pn随着水分含量增加而增加,但是在80%～95%时,Pn随水分含量增加而下降,光合最适水分含量约70%～80%;另一种出现在湿地匍灯藓,水分含量20%～80%时,Pn随着水分含量增加而增加,在80%～95%时,Pn维持一个较高的水平,光合最适水分含量为80%～90%。在一个大的水分含量范围内（60%～95%）,暗呼吸（Rd）保持相对稳定,但是在水分含量较低时（20%～70%）,Rd随着水分含量的下降而下降。在藓体水分含量与水势之间的关系方面,3种藓类植物相似,水分含量与水势对数之间的回归曲线为S形曲线。     

铅和镉污染对大羽藓生理特性的影响

This paper dealt with the effects of ²⁺,²⁺ and their combined pollution on the contents of chlorophyll,potassium and calcium in Thuidium cymbifolium.The results showed that except at 0.1 mg ²⁺稬^-1,the chlorophyll content decreased with increasing ²⁺ and ²⁺ concentrations,which was 18% of the control at 100 mg ²⁺稬^-1,and decreased by 48.6% at 200 mg ²⁺稬^-1.The potassium and calcium contents also decreased with increasing pollutants concentrations,being decreased by 61.1% at 100 mg ²⁺稬^-1.²⁺ had a stronger toxicity than ²⁺,and the toxicity of their combined pollution was stronger than that of each pollutant.²⁺ could increase the toxicity of ²⁺.     

两种匍灯藓属植物夏季和冬季光合特性的比较研究

分别对生长于冬季和夏季的五倍子蚜虫冬寄主藓类植物湿地匍灯藓(Plagiomniumacutum(Lindb.)T.Kop.)和侧枝葡灯藓(Plagiomnium maximoviczii(Lindb.)T.Kop.)的净光合速率及其与光照、温度的关系进了比较研究.结果表明,2种藓类的最大光合能力在夏季分别为125.67和94.63μmolCO2     

高温胁迫下两种藓类植物过氧化物酶活性的变化

在不同的高温胁迫条件下 ,对湿地匍灯藓 (Plagiomnium acutum)和大羽藓 (Thuidium cymbifolium)过氧化物酶 (POD)活性及其与处理时间和处理温度的关系进行了初步研究。结果表明 ,在一定的温度范围内 ,随着温度的升高 ,POD活性增加 ,二者成线形关系。在一定温度条件下 ,一般随着处理时间的延长 ,POD活性增加。但是当超过一定的温度 (4 5～ 5 0°C)以及一定的处理时间 (4～ 6h) ,POD活性有所下降。结果还表明 ,湿地匍灯藓的POD活性显著高于大羽藓。而且在高温胁迫下 ,湿地匍灯藓 POD活性变化比大羽藓活跃 ,其变化幅度也比大羽藓大。     

Pb、Cd污染胁迫对大羽藓超微结构的影响

大羽藓在Ph、Cd溶液中培养7d后,观察其超微结构的变化发现：Pb、Cd胁迫使得细胞的超微结构遭到破坏,如叶绿体的外膜破裂,不连续,甚至完全消失;类囊体片层膨胀,或高浓度培养中叶绿体完全解体;线粒体外膜断裂或消失;细胞核被膜破坏,染色质凝聚,核质解体。仅在Cd100mg／L的培养中观察到内质网断裂呈片段状。同时在Pb的培养中发现了大量的黑色颗粒,而在Cd的培养中却未发现。     

人工与自然恢复条件下地被层优势种大羽藓的遗传多样性比较

基于随机扩增多态性DNA(RAPD)方法比较了川西米亚罗地区3个人工云杉林样地和3个天然次生林样地大羽藓(Thuidium cym bifolium)种群的遗传多样性及分化程度。人工林种群的平均多态位点百分比(PPL)为12.7%,Ne i’s基因多样性(HE)为0.042,Shannon’s信息指数(S)为0.064,种群内遗传一致度(I)为0.952;天然次生林种群则依次为10.0%、0.027、0.043和0.960。人工林种群和天然次生林种群Gst分别为0.592和0.702,Fst分别为0.639和0.695;结合UPGMA聚类和PCA分析,发现种群间的基因交流极少。单因素方差分析显示,人工林下大羽藓种群的遗传多样性水平显著高于天然次生林下种群(p<0.05),表明在皆伐迹地上通过人工造林能有效地促进林下物种遗传多样性的恢复。     

A model of the seasonal pattern of carbon acquisition in two woodland herbs,Mercurialis perennis L. and Geum urbanum L.

Summary Seasonal changes in the light and temperature dependence of photosynthesis were investigated in field grown plants of Mercurialis perennis and Geum urbanum. In both species changes in photosynthetic capacity were closely related to the development of the overstorey canopy. In G. urbanum there was a marked shift in the temperature dependence of photosynthesis through the season whereas no such pattern was found in M. perennis. Model predictions of field rates of photosynthesis were made using the measurements of light and temperature dependence in the laboratory and validated against field observations. Long term continuous records of light and temperature in the field were used in conjunction with the model to make predictions of carbon acquisition in shoots of the two species through the season. These calculations indicated that G. urbanum was able to take advantage of high light levels just prior to canopy closure through a combination of high photosynthetic capacity, the ability to maintain photosynthesis at relatively low temperatures and the presence of overwintering leaves. In M. perennis leaf development was early enough to utilise the high spring light period. After canopy closure M. perennis maintained a higher average rate of CO₂ flux due to a combination of high apparent quantum efficiency and low rates of respiration.     

不同水分条件下三种附生地衣的光合作用特性

附生地衣是哀牢山湿性常绿阔叶林生态系统中重要的结构性组分。通过对该区域山地森林中3种典型附生地衣平滑牛皮叶 (Sticta nylanderiana)、网肺衣 (Lobaria retigera) 和橄榄斑叶 (Cetrelia olivetorum)在不同水分条件下的光合光响应及荧光参数的测定分析,结果显示,附生地衣光补偿点 (LCP)、光饱和点 (LSP)较高,对强光适应能力较强。在水分胁迫 (含水量5%~10%) 条件下,3种附生地衣的最大净光合速率 (Pmax) 仅为17~50nmol·g-1·s-1。随着含水量的增加,地衣的最大净光合速率 (Pmax) 与暗呼吸速率 (Rday) 逐渐增大,LCP降低,而LSP随之提高,这表明3种附生地衣具备“阳生植物”的某些特性,从而能够在一定程度上适应野外光照较强的灌丛、向阳林冠等生境。地衣叶绿素光反应中心初始荧光参数 (F0) 和最大光化学效率 (Fv/Fm) 随含水量下降而显著降低,暗示其光反应中心对水分有很强的敏感性。水分条件的改善有助于附生地衣的光反应中心进入到较高的生理活性状态。     

Photosynthetic limitations of a halophyte sea aster (<Emphasis Type="Italic">Aster tripolium</Emphasis> L) under water stress and NaCl stress

To understand the mechanisms of salt tolerance in a halophyte, sea aster (Aster tripolium L.), we studied the changes of water relation and the factors of photosynthetic limitation under water stress and 300 mM NaCl stress. The contents of Na⁺ and Cl^- were highest in NaCl-stressed leaves. Leaf osmotic potentials (Ψ _s) were decreased by both stress treatments, whereas leaf turgor pressure (Ψ _t) was maintained under NaCl stress. Decrease inΨ _s without any loss ofΨ _t accounted for osmotic adjustment using Na⁺ and Cl^- accumulated under NaCl stress. Stress treatments affected photosynthesis, and stomatal limitation was higher under water stress than under NaCl stress. Additionally, maximum CO₂ fixation rate and O₂ evolution rate decreased only under water stress, indicating irreversible damage to photosynthetic systems, mainly by dehydration. Water stress severely affected the water relation and photosynthetic capacity. On the other hand, turgid leaves under NaCl stress have dehydration tolerance due to maintenance of Ψ _t and photosynthetic activity. These results show that sea aster might not suffer from tissue dehydration in highly salinized environments. We conclude that the adaptation of sea aster to salinity may be accomplished by osmotic adjustment using accumulated Na⁺ and Cl^-, and that this plant has typical halophyte characteristics, but not drought tolerance. Electronic Publication     

Overview of the physiological ecology of carbon metabolism in seagrasses

The small but diverse group of angiosperms known as seagrasses form submersed meadow communities that are among the most productive on earth. Seagrasses are frequently light-limited and, despite access to carbon-rich seawaters, they may also sustain periodic internal carbon limitation. They have been regarded as C3 plants, but many species appear to be C3–C4 intermediates and/or have various carbon-concentrating mechanisms to aid the Rubisco enzyme in carbon acquisition. Photorespiration can occur as a C loss process that may protect photosynthetic electron transport during periods of low CO₂ availability and high light intensity. Seagrasses can also become photoinhibited in high light (generally>1000 μE m⁻² s⁻¹) as a protective mechanism that allows excessive light energy to be dissipated as heat. Many photosynthesis–irradiance curves have been developed to assess light levels needed for seagrass growth. However, most available data (e.g. compensation irradiance I_c) do not account for belowground tissue respiration and, thus, are of limited use in assessing the whole-plant carbon balance across light gradients. Caution is recommended in use of I_k (saturating irradiance for photosynthesis), since seagrass photosynthesis commonly increases under higher light intensities than I_k; and in estimating seagrass productivity from H_sat (duration of daily light period when light equals or exceeds I_k) which varies considerably among species and sites, and which fails to account for light-limited photosynthesis at light levels less than I_k. The dominant storage carbohydrate in seagrasses is sucrose (primarily stored in rhizomes), which generally forms more than 90% of the total soluble carbohydrate pool. Seagrasses with high I_c levels (suggesting lower efficiency in C acquisition) have relatively low levels of leaf carbohydrates. Sucrose-P synthase (SPS, involved in sucrose synthesis) activity increases with leaf age, consistent with leaf maturation from carbon sink to source. Unlike terrestrial plants, SPS apparently is not light-activated, and is positively influenced by increasing temperature and salinity. This response may indicate an osmotic adjustment in marine angiosperms, analogous to increased SPS activity as a cryoprotectant response in terrestrial non-halophytic plants. Sucrose synthase (SS, involved in sucrose metabolism and degradation in sink tissues) of both above- and belowground tissues decreases with tissue age. In belowground tissues, SS activity increases under low oxygen availability and with increasing temperatures, likely indicating increased metabolic carbohydrate demand. Respiration in seagrasses is primarily influenced by temperature and, in belowground tissues, by oxygen availability. Aboveground tissues (involved in C assimilation and other energy-costly processes) generally have higher respiration rates than belowground (mostly storage) tissues. Respiration rates increase with increasing temperature (in excess of 40°C) and increasing water-column nitrate enrichment (Z. marina), which may help to supply the energy and carbon needed to assimilate and reduce nitrate. Seagrasses translocate oxygen from photosynthesizing leaves to belowground tissues for aerobic respiration. During darkness or extended periods of low light, belowground tissues can sustain extended anerobiosis. Documented alternate fermentation pathways have yielded high alanine, a metabolic ‘strategy’ that would depress production of the more toxic product ethanol, while conserving carbon skeletons and assimilated nitrogen. In comparison to the wealth of information available for terrestrial plants, little is known about the physiological ecology of seagrasses in carbon acquisition and metabolism. Many aspects of their carbon metabolism — controls by interactive environmental factors; and the role of carbon metabolism in salt tolerance, growth under resource-limited conditions, and survival through periods of dormancy — remain to be resolved as directions in future research. Such research will strengthen the understanding needed to improve management and protection of these environmentally important marine angiosperms.     

Use of a novel two-stage cultivation method to determine the effects of environmental factors on the growth and sporulation of several biocontrol fungi

To supply essential information for improving mass production and biocontrol efficacy, two-stage cultivation on agar plates was used to evaluate the environmental conditions affecting mycelial growth and sporulation of seven biocontrol fungi. Maximum growth and sporulation occurred on acid media for Paecilomyces (Pa.) lilacinus IPC-P, Pochonia (Po.) chlamydosporia HSY-12-14, and Lecanicillium lecanii CA-1-G, and on alkaline media for Metarhizium anisopliae isolates. All fungi preferred a certain water potential and temperature for sporulation. Light greatly inhibited the growth of P. lilacinus IPC-P, M. anisopliae SQZ-1-21, and L. lecanii CA-1-G but enhanced the sporulation of P. lilacinus M-14, P. chlamydosporia HSY-12-14, and L. lecanii CA-1-G.