内蒙古东胜延安组孢粉研究

本文报道了内蒙古东胜侏罗纪含煤地层延安组的孢粉组合,共记述孢子花粉６２属１２５种,疑源类２属４种,描述了８新种,２新组合种。通过对孢粉类型时空分布,兴衰变化的研究及与国内外相关孢粉组合比较,推断东胜延安组时代为中侏罗世早期（Ａａｉｅｎｉａｎ－Ｂａｊｏｃｉａｎ期）。根据化石孢子花粉可能的植物亲缘关系以及这些植物生态条件,推测当时东胜地区存在以苏铁科、银杏科、松柏纲植物和桫椤科树蕨为主体,很多草本和木本蕨类参与其中的茂盛植物群,气候属温暖湿润的亚热带—温带型。     

新疆温泉煤田早、中侏罗世孢粉组合及其地层意义*

新疆温泉煤田艾肯拜尔段和柯克它乌组的孢粉化石,计有42属59种.根据孢粉类型和含量变化等特征,建立2个孢粉组合(自下而上):1. Dictyophyllidites-Chordasporites-Jugasporites 组合;2. Cyathidites-Neoraistrickia-Pseudopicea 组合.第一组合产于艾肯拜尔段,时代可能为早侏罗世,第二组合产于柯克它乌组,时代暂定为早、中侏罗世.根据孢粉组合反映的植物群面貌是:裸子植物非常茂盛,其中以松柏纲为主,蕨类植物较少(包括真蕨纲植物);反映的古气候属于温暖湿润的亚热带型.     

新疆库车牙哈井下克孜勒努尔组底部孢粉组合

本文是对于新疆库车县牙哈乡进下中侏罗世早期克孜勒努力尔库部孢粉组合的研究,共计有孢粉２４属３２种,藻类化石２属３种,其Ｔｒｉｌｏｂｏｓｐｏｒｉｔｅｓ ａｎｔｉｑｕｕｓ亦见于库车河和阳霞河露头剖面的克孜勒努力尔组底部,推测层位较为稳定。根据孢粉组合认为地质时代为中侏罗世早期,同时根据孢粉植物群反映的古气候属于温暖湿润的亚热带型。     

内蒙古东胜中侏罗世延安组孢粉组合

研究了内蒙古东胜罕台川、碾盘梁沟和柳沟3个剖面中侏罗世孢子花粉化石34属63种, 包括2个新种. 基于10个样品中发现的3 863粒孢子花粉化石的鉴定和统计, 建立东胜地区延安组孢粉组合.该组合中蕨类植物孢子有19属37种, 含量占46%～49%, 最低为39%.裸子植物花粉略占优势, 有15属26种,含量为51%～54%, 最高达61%.与国内外相关资料对比结果表明该孢粉组合的地质时代应属中侏罗世巴柔期.孢粉植物群反映研究区在中侏罗世早期为暖温带或亚热带的暖湿气候.     

内蒙古东胜中侏罗世延安组孢粉组合

研究了内蒙古东胜罕台川、碾盘梁沟和柳沟 3个剖面中侏罗世孢子花粉化石 34属 6 3种 ,包括 2个新种。基于 10个样品中发现的 386 3粒孢子花粉化石的鉴定和统计 ,建立东胜地区延安组孢粉组合。该组合中蕨类植物孢子有 19属 37种 ,含量占 46 %～ 49% ,最低为 39%。裸子植物花粉略占优势 ,有 15属 2 6种 ,含量为 5 1%～ 5 4% ,最高达 6 1%。与国内外相关资料对比结果表明该孢粉组合的地质时代应属中侏罗世巴柔期。孢粉植物群反映研究区在中侏罗世早期为暖温带或亚热带的暖湿气候     

湖北秭归盆地中侏罗世陈家湾组孢粉组合的发现及其意义

本文首次报道了湖北秭归盆地陈家湾组孢粉组合,该组合可归入Cyathidites minor-Classopollis Callialasporites为代表的组合,时代属中侏罗世。陈家湾组孢粉组合的特征反映了秭归盆地中侏罗世泄滩组、陈家湾组和沙溪庙组三个组的孢粉组合的面貌基本一致,仅早期组合与中、晚期组合略有差别。建议以Gyathidites minor-classopollis-callialasportes组合代表湖北西部——重庆地区中侏罗世孢粉组合,早期为Lunzisporites pallidus亚组合,中晚期为Converrrcosisporites venitus亚组合。根据孢粉植物群在本区侏罗纪垂直分布情况,提出早侏罗世时期属亚热带一热带炎热潮湿气候环境,植物生长茂盛;早侏罗世之后,潮湿的气候仍占主导地位,但出现了干旱的先兆;中侏罗世早期进入了半干旱阶段,随后即为炎热干旱的气候所笼罩;至晚侏罗世达到非常干旱的程度,植物种类十份单调,唯有掌鳞杉科植物占据着统治地位。     

新疆三塘湖盆地塘浅3井早侏罗世孢粉组合

本文对在新疆三塘湖盆地塘浅3井701－834m层段发现的孢粉植物群进行了系统的分析研究,共获孢粉45属93种（包括1新种）,疑源类化石5属5种及一个未定类型,组成以Osmundacidites-Piceites-Pinuspollenites-Quadraeculina为主的孢粉组合,根据孢粉组合特征,认为其时代应归为早株罗世晚期,对组合中主要孢粉属种可能的母体植物的生长环境进行分析,推测新疆三塘湖地区在早侏罗世晚期为温带－亚热带气候。     

新疆三塘湖盆地塘浅3井中侏罗世孢粉组合

本文对在新疆三塘湖盆地塘浅3井106-701m层段发现的孢粉化石进行了系统的分析研究,共获孢子花粉52属120种（包括相似种和未定种）,疑源类化石2属2种及一个未定类型,根据孢粉属种及其含量的变化,自下而上分为两套组合;1）Cyathidites minor-Osmundacidites-Cycadopites-Quadraeculina组合;2）Kraeuselisporites ma-nasiensis-Classopollis-Quadraeculina组合,第一组合产于该井413-710m层段。时代归为中侏罗世早期,赋存地层相当于西山窑组;第二组合产于106-413m,时代归为中侏罗世晚期,赋存地层相当于头屯河组,系统分析组合中主要孢粉属种及其母体植物的生长环境,推测新疆三塘湖盆地及其周围地区在中侏罗世早期为温带或亚热带气候,晚期为亚热带气候。     

甘肃平凉安国镇白垩系六盘山群的孢粉植物群

对甘肃—宁夏交界处六盘山群一个露头剖面进行了孢粉分析,从和尚铺组、李洼峡组、马东山组和乃家河组中获得了孢粉化石。这些材料表明,六盘山群的孢粉植物群中白垩纪分子丰度高、分异度大,时代可能为晚Aptian—早、中Albian。孢粉反映当时的气候条件中性偏干,其中和尚铺组和乃家河组比李洼峡组和马东山组要更干一些。根据孢粉资料,六盘山群的和尚铺组至乃家河组的沉积可与盆地主体的志丹群的上部即泾川组对比,三桥组则可能相当于罗汉洞组。陕甘宁盆地西部边缘区缺少相当于志丹群宜君组至环河华池组的早白垩世早期的沉积。     

西藏新生代秋乌组孢粉化石的发现及其初步研究

本文首次报道西藏雅鲁藏布江缝合带附近秋乌组含煤沉积中的孢粉化石。孢粉植物群主要由Quercoidifes,具孔类及三孔沟类花粉组成,包括12科26属及一些未定类群。组合中产有少量的Graminidites及Tsugaepollenites。植物群的总体特征显示其时代可能为渐新世至早中新世。秋乌组沉积早期的环境比较温暖。     

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.     

Monovalent Cation Permeation through the Connexin40 Gap Junction Channel : Cs,Rb, K,Na, Li,TEA, TMA,TBA, and Effects of Anions Br,Cl, F,Acetate, Aspartate,Glutamate, and NO3

The unitary conductances and permeability sequences of the rat connexin40 (rCx40) gap junction channels to seven monovalent cations and anions were studied in rCx40-transfected neuroblastoma 2A (N2A) cell pairs using the dual whole cell recording technique. Chloride salt cation substitutions (115 mM principal salt) resulted in the following junctional maximal single channel current-voltage relationship slope conductances (γ_j in pS): CsCl (153), RbCl (148), KCl (142), NaCl (115), LiCl (86), TMACl (71), TEACl (63). Reversible block of the rCx40 channel was observed with TBA. Potassium anion salt γ_j are: Kglutamate (160), Kacetate (160), Kaspartate (158), KNO₃ (157), KF (148), KCl (142), and KBr (132). Ion selectivity was verified by measuring reversal potentials for current in rCx40 gap junction channels with asymmetric salt solutions in the two electrodes and using the Goldman-Hodgkin-Katz equation to calculate relative permeabilities. The permeabilities relative to Li⁺ are: Cs⁺ (1.38), Rb⁺ (1.32), K⁺ (1.31), Na⁺ (1.16), TMA⁺ (0.53), TEA⁺ (0.45), TBA⁺ (0.03), Cl⁻ (0.19), glutamate⁻ (0.04), and NO₃− (0.14), assuming that the monovalent anions permeate the channel by forming ion pairs with permeant monovalent cations within the pore thereby causing proportionate decreases in the channel conductance. This hypothesis can account for why the predicted increasing conductances with increasing ion mobilities in an essentially aqueous channel were not observed for anions in the rCx40 channel. The rCx40 effective channel radius is estimated to be 6.6 Å from a theoretical fit of the relationship of relative permeability and cation radius.     

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.     

Reliability of Analyses of Hg,Fe, Ca,K, P,pH, Alkalinity,Conductivity, Hardness and Colour from Lakes

The aim of this report has been to present results concerning analytical quality controls of Hg analysis of fish and sediment, analyses of Fe, Ca, total-P, K, pH, alkalinity, conductivity, colour and hardness (Ca + Mg) of lake water samples. Despite the fact that these are standard parameters in many regular water control programs, there are major differences in the reliability with which these parameters can be determined. The focus here is on an overall inter-laboratory comparison between the parameters. Six laboratories have been involved in the analysis. Selected results: pH gives the lowest (average) relative standard deviation (error), about 2 %; conductivity gives an error of about 5–7 %; alkalinity yields an average error of as much as 13–25 %, which is the largest among the parameters studied here; colour also gives a high error, 9–15 %; hardness gives a relative standard deviation of about 6–7 %. Of the other parameters (i. e., Hg, Fe, Ca and P), Hg gives the best reliability and Fe and P the lowest. To have knowledge of the reliability of the analytical data is of paramount importance in most control programs and research projects.     

Competitive inhibition and selectivity enhancement by Ca in the uptake of inorganic elements (Be, Na, Mg, K, Ca, Sc, Mn, Co, Zn, Se, Rb, Sr, Y, Zr, Ce, Pm, Gd, Hf) by carrot (Daucus carota cv. U.S. harumakigosun)

We investigated the uptake of inorganic elements (Be, Na, Mg, K, Ca, Sc, Mn, Co, Zn, Se, Rb, Sr, Y, Zr, Ce, Pm, Gd, and Hf) and the effect of Ca on their uptake in carrots (Daucus carota cv. U.S. harumakigosun) by the radioactive multitracer technique. The experimental results suggested that Na, Mg, K, and Rb competed for the functional groups outside the cells in roots with Ca but not for the transporter-binding sites on the plasma membrrane of the root cortex cells. In contrast, Y, Ce, Pm, and Gd competed with Ca for the transporters on the plasma membrane. The selectivity, which was defined as the value obtained by dividing the concentration ratio of an elemental pair, K/Na, Rb/Na, Be/Sr, and Mg/Sr, in the presence of 0.2 and 2 ppm Ca by that of the corresponding elemental pair in the absence of Ca in the solution was estimated. The selectivity of K and Rb in roots was increased in the presence of Ca. The selectivity of Be in roots was not affected, whereas the selectivity of Mg was increased by Ca. These observations suggest that the presence of Ca in the uptake solution enhances the selectivity in the uptake of metabolically important elements against unwanted elements.     

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.