澳门青洲山白楸+假苹婆+破布叶群落特征研究

采用样方调查法对澳门青洲山白楸（Mallotus paniculatus）＋假苹婆（Sterculia lanceolata）＋破布叶（Microcos paniculata）群落的种类组成、外貌、结构特征、区系和物种多样性进行了分析,结果表明,1700m2样方中有维管植物70种,隶属于42科65属,其中热带性分布属占90.32%,群落属于南亚热带常绿阔叶林植被类型。群落外貌常绿,生活型以藤本高位芽为主（占22.86%）。群落的物种丰富度Magarlef指数为8.78,Shannon-Wienner指数为2.22,Simpson指数为0.98,均匀度Pielou指数为0.52。群落各层次的丰富度、Simpson指数以及Shannon-Wienner指数均表现为下木层〉乔木层〉藤本植物〉草本层,均匀度表现为藤本植物〉乔木层〉下木层〉草本层,表明下木层中组成的种类较乔木层多,优势树种较乔木层明显。     

舟山岛东部地区小型兽类的群落组成与动态分析

１９９０年７月至１９９２年１２月在浙江舟山岛东部地区每月定点调查小型兽类的群落组成和数量动态。该地区可划分为室内、房周围、稻田区、山地和山林等五类生境的５个小兽群落。群落相似性指数以稻田区的黑线姬鼠＋黄毛鼠群落与山地的黑线姬鼠＋黄毛鼠群落最高,多样性指数和均匀性指数以房周围臭Ｑｕ＋黄毛鼠＋褐家鼠群落最高。各群落的全年数量动态可分为双峰型（室内和山地生境）与单峰型（其余３种生境）。对各群落种类组成的     

洪湖主要沉水植物群落的定量分析：Ⅱ.微齿眼子菜＋穗花狐尾藻＋轮藻群落

微齿眼子菜＋穗花狐尾藻＋轮藻群落是洪湖的一个特殊沉水植物群落类型,其形成和维持与圈养活动及特殊的环境条件密切相关,该群落种类组成简单,组成种分布均一,一秋季峰值为２５１ｇｍ＾－１（干重）,季节最大生物量为春季３１２ｇｍ＾－１（干重）。策齿子菜在生物量为秋季１５２ｇｍ＾－１（干重）,穗花狐尾藻季节最大生物量为冬季４５ｇｍ＾－１（干重）,轮藻季节最大生物量为春季１７８ｇｍ＾－１（干重）。群落水平结果     

洪湖主要沉水植物群落的定量分析Ⅲ.金鱼藻+菹草+穗花狐尾藻群落

金鱼藻＋菹草＋穗花狐尾藻群落是洪湖生物量最大的沉水植被类型,在不同的地段存在较大的变化,种类组成复杂,金鱼藻和菹草在不同有季节交替成为群落的优势种。水流是影响不同种群水平分布的主要因素。从水面到水底,植被郁闭度逐步降低。各种对之间不存在显著的联结关系,水流作用及各有关种营养繁殖体的散布方式使得某些种对的生物量分布在一定时期出现显著的相关关系。     

黔西北地区农田鼠类群落结构的研究

本文根据黔西北地区农田鼠类的种类组成和数量,将该地区农田鼠类划分为如下４个鼠类群落：Ａ．高山姬鼠＋社鼠群落,Ｂ．黑线姬鼠＋锡金小家鼠＋高山姬鼠群落,Ｃ．黑线姬鼠＋大足鼠＋锡金小家鼠群落和Ｄ．黑线姬鼠＋小家鼠群落。在群落Ｂ中多样性指数（１．４３３）和均匀性指数（０．６８９）最高,最低是群落Ａ,分别为０．８８９和０．４５７;最高的优势度指数（０．５０５）是群落Ａ,而群落Ｂ是０．３０３为最低;群落Ｂ和群落Ｃ之间的相似性指数（０．７５０）最高,群落Ａ和群落Ｄ之间是０．０７５为最低。     

羊草＋杂类草群落数量特征季节动态的研究

本文对肇州羊草＋杂类草群落主要种群、种组及群落数量特征季节动态进行了探讨。结果表明,在生长季内,羊草、蔓委陵菜群种及丛生禾草种组高度和盖度,群落的盖度及密度特征呈单峰型变化,群落最大地上生物量出现在８月５日,其值为１９７３ｇ／ｍ２干物质,而后下降;在生长季内,符合拓广了的Ｌｏｇｉｓｔｉｃ模型增长,其模型为：Ｂ＝２２４６０３８１＋ｅ５．９２８９－５．５３８８×１０２·ｔ－４．８４８４×１０４·ｔ２＋３．５３６５×１０－６·ｔ３     

鲁西、南平原农作区小型兽类群落组成及季节变化

作者于１９９２年３月至１９９３年３月在鲁西和鲁南平原农作区对小型兽类群落进行了调查,其群落组成以啮齿动物为主,可划为６类群落：河滩高他的黑线仓鼠群落,河滩高地人房附近的黑线仓鼠＋小家鼠群落,缓平坡地的黑线仓鼠＋黑线姬鼠群落,浅平洼地的黑线姬鼠＋黑线仓鼠＋大仓鼠群落,洼地农作区的黑线仓鼠＋黑线姬鼠＋大仓鼠群落和洼地蔬菜种植区的黑线姬鼠＋黑线仓鼠群落。群落的季节变化明显,１１月至次年２月以黑线仓鼠为优势种,其它月份则黑线姬鼠或大仓鼠较多;人房附近农作区小家鼠也有季节性迁移现象。     

梁子湖水——陆交错区水生植物群落生态学研究

对梁子湖水－陆交错区中植物群落的的组成、结构、生长型和生物量进行了测定,结果表明交错区内共分布有9种植物群落：1）微齿眼子菜（Potamogeton maackianus)群落;2）狐尾藻（Myriophyllum spicatum)＋苦草（Vallis-neria natans)＋金鱼藻（Ceratophyllum denersum）群落;3）微齿眼子菜＋金鱼藻群落;4）金鱼藻＋狐尾藻＋微齿眼子菜群落;5）金鱼藻＋狐尾藻＋荇菜（Nymphyoides pettlatum)群落;6）水蓼（Polygonum hydropiper)＋菱（Trapa bipinosa）＋菰（Zizania latifolia)群落;7）菹草（Potamogeton crispus)群落;8）菰＋荇菜＋蓼群落;9）湿生植物(Helophyte）群落。主要植物群4落生物量：狐尾藻＋苦草＋金鱼藻群落2414g.m^-2。金鱼藻＋狐尾藻＋微齿眼子菜群落4379g.m^-2,微齿眼子菜＋金龟藻群落1486g.m^-2,微齿眼子菜群4落2805g.m^-2。交错区内主要植物群落生量的季节变化与群落内优势种的生长方式、人为活动的干扰以及个体生态特征密切相关。群落内优势物种的水平分布表现为均匀分布和群聚分布两种方式。     

海南岛霸王岭热带山地植被研究：Ⅱ.代表群落类型的结构分析

以陆均松＋黄叶树一线枝蒲桃群落和钝叶水丝梨＋线枝蒲桃一托盘青冈群落为例,对海南岛霸王岭自然保护区域内的热带山地雨林和热带山地常绿林植被的最小取样面积、种群的立木级组成以及物种重要值作了初步的分析。     

浙江天童苦槠+白栎灌丛群落的生物量研究

采用直接收获法研究了浙江天童地区苦槠＋白栎次生灌丛群落的地上部分生物量。结果表明该区次生灌丛的地上部分生物量为16．77t/hm^2,还不到常绿阔叶林幼林生物量（地上部分）的1／3。次生灌丛生物量的分布,从群落层次上看,主要集中于藻木层;从垂直高度上看,主要分布在0－4m之间;从种类组成上看,主要分布于苦槠、白栎、山矾、茅栗等优势种中。根据生物量的研究,文中还对如何加速次生灌丛的进展演替进行了讨论。     

Energy-dependent exchange of K+ in heart mitochondria. K+ influx.

The tuberculostatic and carcinogenic drug isonicotinic acid hydrazide (“isoniazid”) is oxidized to pyridine-4-carboxaldehyde by the horseradish peroxidase/Mn²⁺/O₂ system. Eosin and related sensitizers greatly accelerate the reaction and generate light detectable with the liquid scintillation counter or with the photon counter. If the isoniazid concentration is raised, the rate and extent of O₂ uptake are increased, but above a certain concentration of isoniazid, emission is reduced and even suppressed. The strong quencher of triplet eosin, potassium ferricyanide, abolished both effects of eosin, that is, catalysis and light emission. Superoxide dismutase at high concentrations partially suppressed the emission and almost totally removed the catalytic effect. It is tentatively proposed that the isoniazid/peroxidase/Mn²⁺/O₂ system efficiently produces the aldehyde in the triplet state, which in turn transfers energy to eosin. Because of the presence of oxygen, only a small yield of triplet eosin is obtained and only a small fraction of these triplet eosin molecules is able to react with isoniazid. Nevertheless, it will contribute efficiently to a cyclic process of oxidation of the isoniazid.     

Energy-dependence exchange of K+ in heart mitochondria. K+ efflux.

The efflux ⁴²K⁺ from isolated beef heart mitochondria under conditions of near steadystate K⁺ is increased by repiration and is sensitive to uncouplers and to exogenous Mg² The respiration-dependent efflux is strongly activated by inorganic phosphate in the presence of external K⁺, but not Na⁺, and is inhibited by oxidative phosphorylation. Low concentrations of mersalyl also activate respiration-dependent efflux of ⁴²K⁺ in the absence of net alteration in matrix K⁺. Acetate in the presence of mersalyl brings about net accumulation of K⁺ with retention of internal ⁴²K⁺. The results are consistent with a model in which nearly constant matrix K⁺ is maintained by the regulated interplay between a K⁺ uniport (which is responsive to membrane potential and which is the pathway for K⁺ influx) and a $\text{K}{}^{\mathrm{+}}\text{H}{}^{\mathrm{+}}$ exchanger (which responds to the transmembrane pH differential and which is the pathway for net K⁺ efflux).     

Cation flux in the ehrlich ascites tumor cell. Evidence for Na+-for-Na+ and K+-for-K+ exchange diffusion.

In a previous study, evidence was presented for an external Na+-dependent, ouabain-insensitive component of Na+ efflux and an external K+-dependent component of K+ efflux in the Ehrlich ascites tumor cell. Evidence is now presented that these components are inhibited by the diuretic furosemide and that under conditions of normal extracellular Na+ and K+ they represent Na+-for-Na+ and K-+for-K+ exchange mechanisms. Using 86Rb to monitor K+ movements, furosemide is shown to inhibit an ouabain-insensitive component of Rb+ influx and a component of Rb+ efflux, both representing approx. 30 percent of the total flux. Inhibition of Rb+ efflux is greatly reduced by removal of extracellular K+. Furosemide does not alter steady-state levels of intracellular K+ and it does not prevent cells depleted of K+ by incubation in the cold from regaining K+ upon warming. Using 22Na to monitor Na+ movements, furosemide is shown to inhibit an ouabain-insensitive component of unidirectional Na+ efflux which represents approx. 22 percent of total Na+ efflux. Furosemide does not alter steady-state levels of intracellular Na+ and does not prevent removal of intracellular Na+ upon warming from cells loaded with Na+ by preincubation in the cold. The ability of furosemide to affect unidirectional Na+ and K+ fluxes but not net fluxes is consistent with the conclusion that these components of cation movement across the cell membrane represent one-for-one exchange mechanisms. Data are also presented which demonstrate that the uptake of alpha-aminoisobutyrate is not affected by furosemide. This indicates that these components of cation flux are not directly involved in the Na+-dependent amino acid transport system A.     

Amiloride-sensitive Na+-H+ antiporter in Escherichia coli.

In everted vesicles of Escherichia coli, delta pH caused by H+ efflux through the Na+/H+ antiporter was measured by using a fluorescent dye. Amiloride inhibited the activity of the Na+/H+ antiporter. Kinetic studies showed that amiloride competed with Na+. The inhibition constant of 40 microM was obtained.     

Compound d+y+ particles of Australia antigen.

Australia antigen (HB8 Ag) particles vary in their antigenic structure. They are generally found to carry either determinant d or determinant y, but not both. This report describes seven sera which contain Australia antigen carrying both d and y on the same particle.     

The effect of Na+ and K+ on the thermal denaturation of Na+ and + K+-dependent ATPase.

To increase our understanding of the physical nature of the Na+ and K+ forms of the Na+ + K+-dependent ATPase, thermal-denaturation studies were conducted in different types of ionic media. Thermal-denaturation measurements were performed by measuring the regeneration of ATPase activity after slow pulse exposure to elevated temperatures. Two types of experiments were performed. First, the dependence of the thermal-denaturation rate on Na+ and K+ concentrations was examined. It was found that both cations stabilized the pump protein. Also, K+ was a more effective stabilizer of the native state than was Na+. Secondly, a set of thermodynamic parameters was obtained by measuring the temperature-dependence of the thermal-denaturation rate under three ionic conditions: 60 mM-K+, 150 mM-Na+ and no Na+ or K+. It was found that ion-mediated stabilization of the pump protein was accompanied by substantial increases in activation enthalpy and entropy, the net effect being a less-pronounced increase in activation free energy.     

S-adenosyl-L-methionine modulates Na+ + K+-ATPase activity in rat colonic basolateral membranes.

Rat colonic basolateral membranes were incubated with S-adenosyl-L-[methyl-3H]methionine (0.3 mM) at 37 degrees C for 2 h at pH 9.0. This resulted in an increase in the specific activity of Na+ + K+-ATPase by 60%. Kinetic parameter analysis revealed a 2-fold increase in the Vmax. of this enzymatic activity, whereas the Km for ATP was unchanged. The methylation inhibitor S-adenosyl-L-homocysteine (2 mM) significantly reduced these S-adenosyl-L-methionine-stimulated increases in specific activity and the Vmax. of Na+ + K+-ATPase. S-Adenosyl-L-methionine treatment of basolateral membranes was also found to significantly increase the fluidity of these preparations, as assessed by steady-state fluorescence polarization techniques using the fluorophore 1,6-diphenyl-1,3,5-hexatriene; S-adenosyl-L-homocysteine (2 mM) again markedly reduced this S-adenosyl-L-methionine-induced increase in fluidity. While transmethylation reactions involving phospholipids, non-polar lipids and proteins were all found to exist in rat colonic basolateral membranes, based on a number of observations, the results of the present studies suggest that transmethylation of membrane phospholipids, but not membrane non-polar lipids or proteins, influenced the fluidity of basolateral membranes which, in turn, modified Na+ + K+-ATPase activity in these membranes.