辽东栎林不同层植物沿海拔梯度分布的DCCA分析

 为研究北京东灵山辽东栎（Quercus liaotungensis）不同层植物的分布与环境因子之间的关系,对东灵山辽东栎林进行了植物群落学调查。沿 海拔梯度在乔木层、灌木层和草本层各调查119个样方,同时调查了每个样方的环境因子如海拔、坡度和坡位。物种数据采用二元属性数据,对 非数值环境因子进行赋值。对东灵山辽东栎林和各环境因子进行去趋势典范对应分析（Detrended canonical correspondence analysis, DCCA）,结果表明：DCCA 第一轴基本上反映了植物群落所处环境的海拔的梯度变化,第二轴基本上反映了坡位的梯度变化。同时发现辽东栎林 大多数植物分布在低海拔区域。乔木层的物种分布比较均匀。草本层的物种分布重叠率是最大的,说明草本植物的生境相似性很高。低海拔区 域的生物多样性要高于高海拔区域的生物多样性。结合环境因子间的相关关系和DCCA排序结果,发现海拔是影响东灵山辽东栎林物种分布的主 要环境因子。     

喀斯特石漠生态系统不同自然演替阶段中苔藓植物多样性特征分析

以“空间代替时间”方法研究了贵州喀斯特石漠地区植被自然恢复演替过程中各演替阶段苔藓植物的群落特征及苔藓植物物种α和β多样性指数。研究结果表明：该区共有苔藓植物群落21种,并以美灰藓（Eurohypnum leptothallum）为优势物种。苔藓植物α多样性指数随演替阶段的发展,表现出先下降、再反弹（藤刺灌丛阶段）、最后再次降低的变化趋势。苔藓植物Pielou均匀度指数的大小表现为：苔藓群落阶段（0.9392）〉 乔灌丛阶段（0.8675）〉 藤刺灌丛阶段（0.8651）〉 草灌丛阶段（0.7677）〉 草丛阶段（0.7676）。β多样性指数（Sorenson多样性指数）分析表明,苔藓植物群落随着演替阶段的发展,相同种类的数目随之减少,群落间相似性系数也逐渐降低。虽然苔藓植物群落在草丛阶段和藤刺灌丛阶段的相似性高于草丛阶段和草灌丛阶段之间的相似性系数,但总的相似性系数却呈现下降趋势。该研究结果可为喀斯特石漠生态系统演替的研究提供依据。     

海南岛热带地区弃荒农田次生植被恢复特点

研究了海南岛热带地区弃荒农田次生植被恢复特点 ,结果表明在热带多雨地区弃荒农田的植被演替过程中 ,植物种数增加的速度较快 ,α多样性指数的增加是比较明显的 ;β多样性变化较强烈的阶段是在草本植物群落与灌丛的过渡区 ,这说明在弃荒农田的植被恢复过程中 ,草本植物群落与灌丛生态过渡区是植物种类增加较快和更替较快的区域。比较弃荒农田植被类型的植物成分百分比与典型原始林和次生林的现有植物成分的百分比 ,预计热带多雨地区弃荒农田 10 0～ 12 0年可达到次生密林     

不同放牧强度下高寒灌丛群落特征和演替规律的数量研究

本文应用多样性指数、聚类分析等数学方法,研究了不同放牧强度下高寒灌丛群落特征的变化,用主分量分析方法,研究了不同放牧强度下高寒灌丛的演替规律。多样性分析结果表明,植物多样性指数在放牧强度为C组的草场达到最大。聚类分析结果,当相关系数R≥0.90 时,以重要值为特征的植物聚合为10类,它们分别属于植物群落不同演替阶段的建群种、优势种和伴生种。主分量分析表明,5个不同放牧强度的高寒灌丛群落聚合为3类,A和B组草场属于以灌木和杂类草为优势植物的2层结构的植物群落,C组草场属于以灌木为建群植物、杂类草和耐牧的莎草为共优势植物的2层结构的植物群落,D和E组草场属于以灌木为建群植物、禾草和莎草为共优势植物的3层结构的植物群落。     

北京东灵山地区植物群落多样性的研究Ⅱ丰富度、均匀度和物种多样性指数

本文以１２５块植物群落调查样地资料为基础,从不同类型、层次的丰富度、均匀度和物种多样性指数及其与海拔的关系等方面对东灵山地区植物群落多样性进行了分析。本区亚高山草甸植物群落多样性沿海拔梯度的变化规律是：物种丰富度和物种多样性指数随海拔升高而下降;物种均匀度则随海拔升高而增加。植物生长型与群落多样性指数的关系表现为“乔木层、灌木层物种丰富度指数相近且明显低于草本层;灌木层和草本层的均匀度指数相近,群落间变异幅度较小,乔本层则变异幅度很大;物种多样性指教则表现出草本层＞乔本层＞灌木层的规律。物种盖度和地上生物量作为测度指标计算群落多样性所得结果相近,且优于以株数作为测度指际计算的结果。     

北京东灵山地区森林的物种多样性和景观格局多样性研究

选取北京东灵山地区暖温带落叶阔叶林中７种主要森林和１个灌丛类型的１１个样方,通过比较这些类型的物种多样性的相关的环境因子,及运用和度分析测度景观格局多样性,揭示了这些类型物种多样性的差异,与环境因子的关系,及其空间分布规律。结果显示：１）各森林类型乔木层物种丰富度均较低,灌木层和草本层物种丰富度较高。大多数森林类型中,物种丰富度的垂直结构是：草本层〉灌木层〉乔木层。２）各森林类型的Ｓｈａｎｎｏｎ指     

鼎湖山植物群落α多样性与环境的关系

用样带取样法,来研究不同取样尺度和不同取样尺度条件下的多个环境因子与鼎湖山植物群落α多样性的关系.取样尺度分别为10、20、40、80m和160m.涵盖鼎湖山主要的植被类型：季风常绿阔叶林、针阔混交林、沟谷常绿阔叶林和针叶林.相关分析和主成分分析结果表明,环境因子对各层次的α多样性的影响程度各不相同,达到显著相关性的取样尺度也不一样,表现出较大的复杂性,同时也表明样带上的环境异质性较高.因此,用海拔梯度作为主要的环境梯度来研究鼎湖山植物群落多样性具有合理性.海拔高度与乔木层多样性的关系在所有取样尺度上都较密切,这说明海拔高度可能是影响乔木层α多样性的最重要环境因子.     

贺兰山东坡典型植物群落多样性垂直分布特征与土壤因子的关系

深入探究山地生态系统植物群落多样性与关键土壤因子的关系及土壤因子在植物群落构建与多样性维持中的重要作用是区域生物多样性保护和生态系统服务功能综合提升的基础。本文采用冗余分析（Redundancy analysis,RDA）和相关分析揭示了贺兰山东坡典型植物群落多样性垂直分布格局与土壤因子的关系。结果表明：（1）贺兰山东坡植物群落多样性具有明显的垂直分布格局,针阔叶混交林植物物种组成最为丰富,中域效应明显;不同层次植物多样性随海拔升高变化趋势不一致且各自在不同海拔间差异显著（P<0.05）,植物多样性大体表现为草本层 > 灌木层 > 乔木层。（2）研究区土壤因子沿海拔梯度变化趋势不同,均存在显著差异（P<0.05）,其中土壤含水量（SM）、有机碳（SOC）和全氮（TN）含量空间变异性较大;高山灌丛草甸土壤养分含量最高,高海拔区土壤P限制高。（3）9个土壤因子解释了研究区总体植物多样性89.68%的生态信息,与植物多样性具有较强的相关性,影响不同层次植物多样性垂直分异的关键土壤因子略有不同。综上,土壤有机碳、pH、碳磷比、含水量是影响贺兰山东坡植物多样性空间分布的主要驱动因子。     

环境因子和干扰强度对高寒草甸植物多样性空间分异的影响

采用样带与样地结合的方法在三江源自然保护区的核心区沿海拔梯度在阴坡、阳坡分别进行草本植被调查,通过因子分析和偏相关分析研究丰富度指数、多样性指数与环境梯度（包括海拔梯度、裸斑面积、坡度、土壤总碳、总氮含量、土壤pH值、土壤总可溶性盐含量）和干扰强度（鼠类干扰强度、放牧强度）之间的关系。研究结果表明：杂类草丰富度指数（DMa杂）与总物种丰富度指数（DMa总）极显著相关（P<0.01）;阳坡DMa杂和DMa总均呈现“中海拔膨胀”现象,阴坡DMa杂和DMa总与海拔梯度呈正相关,莎草科和禾本科的丰富度指数（DMa莎和DMa禾）随海拔升高并无明显规律;通过主成分分析,及偏相关分析,第一主成分（裸斑面积、鼠类干扰和放牧强度）与除莎草科Margalef丰富度指数、禾本科Simpson指数和禾本科Pielou均匀度指数外的其他草地多样性指数均显著相关,是影响阳坡草地植物多样性的主要因子,土壤总碳、总氮含量对阳坡禾本科类群的多样性指数和均匀度指数有极显著影响,土壤pH值、TDS含量和坡度对阳坡莎草科类群的丰富度有显著影响;海拔梯度、土壤总碳、总氮以及pH值对阴坡草本植物群落的多样性影响较大。研究结论认为,植物群落生物多样性的空间分异特征是地理环境、土壤环境以及干扰强度等因素综合作用的结果。无干扰或干扰较弱时,物种多样性主要受土壤环境状况所影响;而在强干扰存在条件下,干扰强度对物种丰富度和多样性的影响比环境因子更显著;遏制高寒草甸植物多样性降低应首先控制放牧及鼠类等强干扰活动。     

盐池四墩子拟步甲昆虫群落组成与环境因子的相关性

2009年3-10月,对宁夏盐池四墩子不同植被类型和人工干扰强度的荒漠草地的拟步甲昆虫群落结构及其环境因子特征进行了调查, 采用多样性指数和典范对应分析(CCA)研究了昆虫群落与环境因子之间的相关性.共收集拟步甲10属20种,5431只,以弯齿琵甲、克小鳖甲和蒙古漠王占优势,分别占总数的47.30%、39.90%和3.59%.CCA分析表明：拟步甲与环境因子之间的相关性高达100%,提示盐池四墩子环境因子变化影响拟步甲的分布,植物群落多样性、植物生物量和土壤含水量对拟步甲昆虫群落的分布影响最大;从物种的分布状况看,谢氏宽漠王对环境最为敏感;小丽东鳖甲、宽突东鳖甲、尖尾东鳖甲、宽腹东鳖甲次之,与植物生物量、植被盖度呈负相关,戈壁琵甲、中华砚甲、网目土甲和淡红毛隐甲与植被密度和土壤含水量呈正相关,蒙古漠王、克小鳖甲、小皮鳖甲和异距琵甲与植物群落多样性呈正相关,奥氏真土甲、弯齿琵甲和达氏琵甲与植物生物量和植被盖度呈正相关;相关和回归分析结果也显示,拟步甲群落的活动密度与土壤含水量极显著正相关(r=0.943,P=0.005).同时,排序反映了拟步甲对生态环境的需求以及其在不同资源维上的生态分化现象.     

Crystal structure, detonation performance, and thermal stability of a new polynitro cage compound: 2, 4, 6, 8, 10, 12, 13, 14, 15-nonanitro-2, 4, 6, 8, 10, 12, 13, 14, 15-nonaazaheptacyclo [5.5.1.13, 11. 15, 9] pentadecane

A new polynitro cage compound 2, 4, 6, 8, 10, 12, 13, 14, 15-nonanitro-2, 4, 6, 8, 10, 12, 13, 14, 15-nonaazaheptcyclo [5.5.1.1(3,11).1(5,9)] pentadecane (NNNAHP) was designed in the present work. Its molecular structure was optimized at the B3LYP/6-31 G(d,p) level of density functional theory (DFT) and crystal structure was predicted using the Compass and Dreiding force fields and refined by DFT GGA-RPBE method. The obtained crystal structure of NNNAHP belongs to the P-1 space group and the lattice parameters are a = 9.99 ?, b = 10.78 ?, c = 9.99 ?, α = 90.01°, β = 120.01°, γ = 90.00°, and Z = 2, respectively. Based on the optimized crystal structure, the band gap, density of state, thermodynamic properties, infrared spectrum, strain energy, detonation characteristics, and thermal stability were predicted. Calculation results show that NNNAHP has detonation properties close to those of CL-20 and is a high energy density compound with moderate stability.     

Distribution of N,P, K,Ca, Mg,S, Zn,Fe, Mn and Cu in groundnut

Summary Concentration of N, P, K, Ca, Mg and S in summer groundnut crop was higher than in kharif while Zn, Fe, Mn and Cu contents were higher in summer crop. Kernel's N, P and Zn; Leaflet's Ca and Mn; Stem's K and Fe; Root's S and Cu and Petiole's Mg contents were highest. Shell's N, P, K, Mg, S, Zn and Cu; Kernel's Ca, Fe and Mn contents were the least. N, P, K, S, Zn and Cu concentrations decreased linearly as the crop grew. Ca, Mg, Fe and Mn concentrations did not display any distinct pattern. Ca concentration was positively correlated with pod yield in both the seasons.     

Simultaneous measurement of the trace elements Al, As, B, Be, Cd, Co, Cu, Fe, Li, Mn, Mo, Ni, Rb, Se, Sr, and Zn in human serum and their reference ranges by ICP-MS

The goal of this article was to establish reference ranges of the concentration of trace elements in human serum and to compare these results with those reported by other authors. We describe the sample preparation and measurement conditions that allow the rapid, precise, and accurate determination of Al, As, B, Be, Cd, Co, Cu, Fe, Li, Mn, Mo, Ni, Rb, Se, Sr, and Zn in human serum samples (n=110) by inductively coupled plasma-mass spectrometry (ICP-MS). Accuracy and precision were determined by analyzing three reconstituted reference serum samples by comparison with other methods and by the standard addition procedure. The advantages of the ICP-MS method include short time of analysis of the elements mentioned, low detection limit, high precision, and high accuracy. Disadventages include a high risk of contamination due to the presence of some of the elements of interest in the environment, the relatively delicate sample handling, and the high cost of the equipment.     

Reference values for the concentrations of As,Cd, Co,Cr, Cu,Fe, I,Hg, Mn,Mo, Ni,Pb, Se,and Zn in selected human tissues and body fluids

This report attempts to formulate reference ranges of elemental concentrations for 15 trace elements in selected human tissues and body fluids. A set of samples consisting of whole blood, blood serum, urine, milk, liver, and hair were chosen and considered for 15 elements of biological significance: As, Cd, Co, Cr, Cu, F, Fe, I, Hg, Mn, Mo, Ni, Pb, Se, and Zn. The results represent wholly or partially data received from 40 countries of the global regions of Africa, Asia, Europe, North, South, and Central America, Australia, and New Zealand. This survey, even if qualitative, has been useful in demonstrating certain trends of trace-element scenarios around the world. It is of course recognized that both diet and environment exert a strong influence on the distribution pattern of several elements, such as As, Cd, Mn, Pb, Se, and Zn. A limited comparison of the available information on soil status of different countries reflected some interesting associations for elements, such as Mn and Zn. Importantly, this study revealed that only a few countries were in a position to identify a reasonable amount of data on samples requested for this project. Regretably, for a number of countries, any dependable data for even such essential elements as Cu, Fe, and Zn were not available. In view of the nutritional importance of many elements, the time is ripe for concerted efforts by intergovernmental agencies to initiate investigations or commission task forces/projects to generate reliable reference data for selected global regions, which sadly lack data of any kind at present.     

Relations of the Al,B, Ba,Br, Ca,Cl, Cu,Fe, K,Li, Mg,Mn, Na,P, S,Si, Sr,and Zn mass fractions to morphometric parameters in pediatric and nonhyperplastic young adult prostate glands

The variation with age of the 18 trace element mass fractions and some histological characteristics of intact prostate glands of 50 subjects aged 0–30 years was investigated by instrumental neutron activation analysis, inductively coupled plasma atomic emission spectrometry, and a quantitative morphometric analysis. Mean values ± standard error of the mean (M ± SΕΜ) for the mass fractions (in milligrams per kilogram wet tissue) of these trace elements in pre-puberty were: Al 28.5 ± 9.0, B 0.40 ± 0.11, Ba 1.48 ± 0.44, Br 10.5 ± 1.5, Ca 241 ± 30, Cl 3,203 ± 278, Cu 3.51 ± 0.89, Fe 33.7 ± 4.1, K 2,364 ± 145, Li 0.020 ± 0.004, Mg 153 ± 23, Mn 0.46 ± 0.06, Na 2,286 ± 130, P 1,391 ± 100, S 1,698 ± 132, Si 62 ± 11, Sr 0.38 ± 0.08, and Zn 27.6 ± 2.3. During puberty and postpuberty, when there is a significant increase in circulating androgens, the mean values were: Al 7.2 ± 1.4, B 0.21 ± 0.05, Ba 0.25 ± 0.06, Br 5.8 ± 1.0, Ca 433 ± 81, Cl 2,314 ± 201, Cu 1.77 ± 0.13, Fe 20.9 ± 1.6, K 2,585 ± 118, Li 0.0088 ± 0.0014, Mg 232 ± 27, Mn 0.34 ± 0.04, Na 1,875 ± 107, P 1,403 ± 98, S 1,673 ± 73, Si 22.2 ± 3.1, Sr 0.22 ± 0.03, and Zn 93.3 ± 8.9. Mean values (M ± SΕΜ) of percent volumes (%) of the stroma, epithelium and lumen in the prostate before puberty were 73.4 ± 2.6, 20.4 ± 1.7, and 4.45 ± 0.94, respectively, versus 46.5 ± 2.5, 38.5 ± 1.9, and 14.9 ± 1.2 during puberty and postpuberty. This work’s results confirm that the Zn mass fraction in prostate tissue is an androgen-dependent parameter. For the first time it has been demonstrated that the glandular lumen is a main pool of Ca, Mg, and Zn accumulation and that the stroma is a main pool of Al, B, Ba, Br, Cl, Cu, Fe, Mn, Na, and Si accumulation in the normal human prostate, for the age range 0–30 years. It was concluded that the Ca, Mg, and Zn binds tightly within the prostatic fluid, because the volume of glandular lumen reflects the volume of prostatic fluid.     

The Effect of Age and Gender on Al, B, Ba, Ca, Cu, Fe, K, Li, Mg, Mn, Na, P, S, Sr, V, and Zn Contents in Rib Bone of Healthy Humans

The effect of age and gender on major, minor, and trace element contents in the intact rib bone of 80 relatively healthy 15–55-year-old women and men was investigated. Contents or upper limit of contents of 16 chemical elements in the rib bone were determined by inductively coupled plasma atomic emission spectrometry (ICP-AES). Mean values (M?±?SΕΜ) for the mass fraction of Ba, Ca, Cu, Fe, K, Li, Mg, Na, P, S, Sr, and Zn (milligram per kilogram of dry bone) were as follows: 2.54?±?0.16, 171,400?±?4,050, 1.35?±?0.22, 140?±?11, 1,874?±?71, 0.049?±?0.011, 2,139?±?38, 5,378?±?88, 75,140?±?1,660, 1,881?±?51, 291?±?20, and 92.8?±?1.5, respectively. The upper limits of contents of Al, B, Mn, and V were <7.20, <0.65, <0.36, and <0.03, respectively. Statistically significant tendency for the Ca, Mg, and P content to decrease with age was found in the human rib bone, regardless of gender. The mass fraction of Fe in the male rib bone increases with age. It was shown that higher Ca, Mg, Na, P, and Sr mass fractions as well as lower Fe content were typical of female ribs as compared to those in male ribs.     

Potential Compounds for Oral Cancer Treatment: Resveratrol,Nimbolide, Lovastatin,Bortezomib, Vorinostat,Berberine, Pterostilbene,Deguelin, Andrographolide,and Colchicine

Oral cancer is one of the main causes of cancer-related deaths in South-Asian countries. There are very limited treatment options available for oral cancer. Research endeavors focused on discovery and development of novel therapies for oral cancer, is necessary to control the ever rising oral cancer related mortalities. We mined the large pool of compounds from the publicly available compound databases, to identify potential therapeutic compounds for oral cancer. Over 84 million compounds were screened for the possible anti-cancer activity by custom build SVM classifier. The molecular targets of the predicted anti-cancer compounds were mined from reliable sources like experimental bioassays studies associated with the compound, and from protein-compound interaction databases. Therapeutic compounds from DrugBank, and a list of natural anti-cancer compounds derived from literature mining of published studies, were used for building partial least squares regression model. The regression model thus built, was used for the estimation of oral cancer specific weights based on the molecular targets. These weights were used to compute scores for screening the predicted anti-cancer compounds for their potential to treat oral cancer. The list of potential compounds was annotated with corresponding physicochemical properties, cancer specific bioactivity evidences, and literature evidences. In all, 288 compounds with the potential to treat oral cancer were identified in the current study. The majority of the compounds in this list are natural products, which are well-tolerated and have minimal side-effects compared to the synthetic counterparts. Some of the potential therapeutic compounds identified in the current study are resveratrol, nimbolide, lovastatin, bortezomib, vorinostat, berberine, pterostilbene, deguelin, andrographolide, and colchicine.