气候变化对我国南方人工林地上生物量影响的模拟研究——以会同生态站磨哨实验林场为例

全球气候变暖对陆地生态系统尤其是森林生态系统有着重要的影响,气温升高、辐射强迫的增强将显著改变森林生态系统的结构和功能.南方人工林作为我国森林的重要组成部分,对气候变化的响应日益强烈.为了探究未来气候情景下我国南方人工林对气候变化的响应,降低未来气候变化对人工林可能带来的损失,本研究采用3种最新的气候情景—典型浓度排放路径情景(RCP2.6情景、RCP4.5情景、RCP8.5情景)预估数据,应用生态系统过程模型PnET-Ⅱ和空间直观景观模型LANDIS-Ⅱ模拟2014—2094年间湖南省会同森林生态实验站磨哨实验林场森林的地表净初级生产力(ANPP)、物种建立可能性(SEP)和地上生物量的变化.结果表明: 不同森林类型的SEP和ANPP对气候变化的响应有明显的差异,各森林类型对气候变化的响应程度表现为: 对于SEP,在RCP2.6和RCP4.5情景下,人工针叶林＞天然阔叶林＞人工阔叶林;在RCP8.5情景下,天然阔叶林＞人工阔叶林＞人工针叶林.对于ANPP,在RCP2.6情景下,人工阔叶林＞天然阔叶林＞人工针叶林;在RCP4.5和RCP8.5情景下,天然阔叶林＞人工阔叶林＞人工针叶林.人工针叶林的地上生物量在2050年左右开始下降,天然阔叶林和人工阔叶林整体呈现上升趋势.2014—2094年,研究区地上总生物量在不同气候情景下增加幅度不同,RCP2.6情景下增加了68.2%,RCP4.5情景下增加了79.3%,RCP8.5情景下增加了72.6%.3种情景下的总地上生物量大小排序为: RCP4.5> RCP8.5> RCP2.6.我们认为,适当的增温将有助于未来研究区森林总地上生物量的积累,但过度的增温也可能会阻碍森林的生产和生态功能的持续发展.     

光照或黑暗条件下野火病菌侵染对烟草光合机构的影响

烟草野火病菌(Pst)是一种兼性营养型的细菌致病菌,它可以引起烟草发生褐色病斑,名为野火病.近年来Pst受到很多关注,然而大多数对Pst的研究主要集中在寄主和非寄主植物对Pst侵染的防御机制和产自于野火病菌的野火毒素上,Pst侵染对烟草叶片光合性能的影响及其机理尚未见报道.研究Pst侵染后对光系统Ⅱ(PSⅡ)的影响不仅可以帮助阐明烟草-Pst 相互作用的机制,还可以从生理角度加深对细菌致病菌病害的了解.本研究采用叶绿素荧光快速诱导动力学曲线分析、类囊体膜蛋白Western分析、活性氧(ROS)和叶绿素含量测定等方法,探讨光照(200 μmol·m^-2·s^-1)或黑暗条件下Pst侵染对烟草光系统Ⅱ的影响.结果表明: 与未处理相比,Pst侵染3 d后在光照和黑暗条件下叶片侵染区域叶绿素含量均显著下降,出现萎黄病变,注射区域呈现出明显的野火病特征.光照和黑暗条件下,侵染3 d后烟草叶片过氧化氢含量明显升高,光照条件下要比黑暗条件下升高比例更大.Pst侵染3 d后,光照和黑暗条件下烟草叶片注射区域叶绿素荧光动力学曲线中K点和J点的相对可变荧光W_K和V_J逐渐增大,叶片最大光化学效率(F_v/F_m)和单位面积有活性反应中心的数目(RC/CSm)均显著下降.此外,相对于光照条件,Pst侵染后在黑暗条件下W_K和V_J的升高程度更大,说明对K点和J点的抑制程度更严重.Pst侵染3 d后,在光照和黑暗条件下放氧复合体(OEC)的核心组分PsaO、光系统Ⅱ反应中心核心蛋白D1蛋白均发生明显的降解,且在黑暗条件下降解更为严重.表明Pst侵染后,在光照和黑暗条件下均会使光合电子传递链Q_A到Q_B的电子传递受到限制,放氧复合体受到伤害,烟草叶片光系统Ⅱ供体侧、受体侧、反应中心的数目和活性均受到伤害,光系统Ⅱ发生光抑制或类似光抑制的伤害,且在黑暗条件下对光系统Ⅱ的伤害程度比光照条件下更为严重.     

VDAC1 serves as a mitochondrial binding site for hexokinase in oxidative muscles

Voltage-dependent anion channels (VDACs), also known as mitochondrial porins, are the main pathway for metabolites across the mitochondrial outer membrane and may serve as binding sites for kinases, including hexokinase. We determined that mitochondria-bound hexokinase activity is significantly reduced in oxidative muscles (heart and soleus) in vdac1^−/− mice. The activity data were supported by western blot analysis using HK2 specific antibody. To gain more insight into the physiologic mean of the results with the activity data, VDAC deficient mice were subjected to glucose tolerance testing and exercise-induced stress, each of which involves tissue glucose uptake via different mechanisms. vdac1^−/− mice exhibit impaired glucose tolerance whereas vdac3^−/− mice have normal glucose tolerance and exercise capacity. Mice lacking both VDAC1 and VDAC3 (vdac1^−/−/vdac3^−/−) have reduced exercise capacity together with impaired glucose tolerance. Therefore, we demonstrated a link between VDAC1 mediated mitochondria-bound hexokinase activity and the capacity for glucose clearance.     

Isolation and Characterization of Photosystem Ⅱ Reaction Center D1-D2-Cytochrome b-559 Complex from the Chloroplasts of Spinach

Photosystem Ⅱ reaction center D1-D2-cytochrome b-559 pigment-protein complex has been isolated and purified from chloroplasts of spinach and its properties have been studied. The Isotared photosystem II reaction center contains close to six chlorophyll a per two pheophytin a molecules. Analysis of fluorescence decaying by phase modulation fluorometry suggests that the reaction center has three components of fluorescence decaying with lifetimes of 1.5 nS, 6.23 nS, 36.26 nS in terms of fractions to total fluorescence yield as 0.06, 0.67, 0.27 respectively. The ,6.25 nS fluorescence component corresponds to chlorophyll a which is energetically uncoupled from the process of charge separation. The proportion of 1.51 nS component is very low, and its source is unclear. The 36.25 nS fluorescence component is attributed to the recombination of the primary radical pair, and so represents the activity of charge separation.     

The Effects of Water Stress on Photosystem Ⅱ in Wheat

The fluorescence yield at room temperature, the capacity of excitation energy distribution between photosystem Ⅰ and Ⅱ by Mg2+, variable fluorescence yield, variable fluorescence quenching rate and fluorescence complementary area were decreased under water stress. These indicated that photosystem Il was impaired. The inhibited variable fluorescence yield could be partly recovered by the addition of artificial electron donor DPC. Therefore, water stress inhibited not only the oxidizing site of photosystem Ⅱ but also impaired partly the reaction center of photosystem Ⅱ.     

Effect of Elevated CO2 on the Primary Conversion of Light Energy of Alfalfa Photosynthesis

In studying the mechanism of increase in alfalfa (Medicago sativa L. ) photosynthesis under elevated atmospheric CO2, it was found that the capacity of chloroplasts for light absorption was greater, the potential activity and efficiency of primary conversion of light enlergy of PS Ⅱ , quantum yield of PS Ⅱ electron transport, and activation capacity of PS Ⅰ were stimulated, photochemical quenching coefficient was increased and non-photochemical quenching coefficient was decreased under elevated atmospheric CO2.     

Mg2+ Induced Fluorescence Change in Relation to Thylakoid Surface Electric Charge in Two Varieties of Soybean Chloroplasts

The effects of Mg2+ concentration on chlorophyll a light-in-duced variable fluorescence and eleetrophoretie velocity of chloroplasts obtained from two varieties of soybean (Ji-Pei No. 1 and Feng-Shou Yellow) were recorded. The light induced variable fluorescence yield and the eleetrophoretie mobility of two kinds of ehloroplasts in the suspending medium containing low level of salt differs from each other. But, the fluorescence yield of chloroplast membranes from two varieties of soybean is relative to that of eleetrophoretic mobility. The pattern of kinetic change of Mg2+ induced variable fluorescence intensity is similar to that of eleetrophoretie mobility. The optimum concentrations of Mg2+ required for the effect on chlorophyll fluorescence and the electrophoretie velocity change are also similar These results indicate that Mg2+ induced excitation energy distribution change between the two photosystems is intimately related to Mg2+-indueed alteration of thylakoil membrane surface eleetrostat.ie property. The possible role of earboxyl group of proteins on Mg2+ induced effects has been discussed in this paper.     

AngⅡ和PKC对心肌细胞AngⅡ 1型受体的转录调节

利用体外培养的心肌细胞,观察血管紧张素Ⅱ（ＡｎｇⅡ）和蛋白激酶Ｃ（ＰＫＣ）在诱导ＡｎｇⅡ１型受体（ＡＴ１）基因表达及蛋白质代谢中的作用．研究结果表明：ＡｎｇⅡ可诱导ＡＴ１ｍＲＮＡ水平一过性下调,呈时间及剂量依赖性,１０ｎｍｏｌ／ＬＡｎｇⅡ刺激细胞６ｈ,引起ＡＴ１ｍＲＮＡ水平降低幅度最大,降至对照的５１．６％±９．５％,然后逐渐回升,２４ｈ恢复至对照水平．３０μｍｏｌ／ＬＨ－７（ＰＫＣ抑制剂）能阻断ＡｎｇⅡ诱导的ＡＴ１ｍＲＮＡ水平的下调．０．３μｍｏｌ／Ｌ的ＰＭＡ（ＰＫＣ激活剂）单独应用可诱导ＡＴ１ｍＲＮＡ水平下调达对照的４３％±８％,加入ＡＴ１拮抗剂ＤＭＰ８１１及Ｄｕｐ７５３均可阻断ＡｎｇⅡ诱导的ＡＴ１ｍＲＮＡ水平的下调．１０ｎｍｏｌ／Ｌ的ＡｎｇⅡ刺激心肌细胞９６ｈ可使蛋白含量降低至对照的７３．４％±５．６％,而加药持续刺激１４４ｈ可使蛋白含量较对照增加３３．８％±６．３％,Ｈ－７不能阻断ＡｎｇⅡ诱导的蛋白含量降低,但可有效地抑制蛋白含量的增加．以上结果提示：ＡｎｇⅡ对心肌细胞ＡＴ１基因的转录和细胞的蛋白代谢有调节作用,而ＰＫＣ则参与了ＡｎｇⅡ的这种调节作用     

基于线粒体COⅡ和Cytb基因序列的8种漠甲系统发育关系

对8种漠甲昆虫线粒体Cytb基因579bp和COⅡ基因585bp的序列片段进行联合分析。结果表明,8种甲虫在长度为1164bp的序列中碱基T,C,A,G的平均含量分别为33.7%,21.2%,33.5和11.6%,A+T平均含量明显高于G+C含量。密码子第三位点A+T含量高达77.2%,而该位点G的平均含量仅为4.0%。序列中碱基替换多发生于第三位点,转换略多于颠换,转换主要以C←T为主,颠换以A←T为主。以土甲族的Eumylada potanini为外群构建的系统发育树表明:漠王和漠甲以很高的置信值聚为一支,二者的关系与Bouchard最新的分类观点相吻合,即漠王族并入漠甲族成为一族;鳖甲族在支序图上另成一支,可视为一个单系群。     

Mitochondrial hexokinase and cardioprotection of the intact heart

The interaction of hexokinase with mitochondria has emerged as a powerful mechanism in protecting many cell types against cell death. However, the role of mitochondrial hexokinase (mitoHK) in cardiac ischemia-reperfusion injury has as of yet received little attention. In this review we examine whether increased binding of hexokinase to the mitochondrion is also an integral component of cardioprotective signalling. We discuss observations in cardiac mitochondrial activation that directed us to the hypothesis of hexokinase cellular redistribution with reversible, cardioprotective ischemia, summarize the data showing that many cardioprotective interventions, such as ischemic preconditioning, insulin, morphine and volatile anesthetics, increase mitochondrial hexokinase binding within the intact heart, and discuss similarities between mitochondrial hexokinase association and ischemic preconditioning. Although most data indicate that mitochondrial hexokinase may indeed be an integral part of cardioprotection, a definitive proof for a causal relation between the amount of mitoHK and cardiac ischemia-reperfusion injury in the intact heart is eagerly awaited. When such relationship is indeed observed, the association of hexokinase with mitochondria will offer an opportunity to develop new therapies to combat ischemic cardiac diseases.