甘肃灵台小石沟晚中新世—上新世小哺乳动物生物地层

根据发现的大量小哺乳动物化石,将甘肃灵台小石沟７２０７４（４）地点剖面划分出４个生物地层带,Ⅰ带与榆社马会组化石组合相当,为中新世晚期;Ⅱ带、Ⅲ带及Ⅳ带代表中国上新世较为完整的小哺乳动物生物地层层序。     

甘肃灵台文王沟晚中新世-早更新世小哺乳动物

大量小哺乳动物化石在地层中的分布,将文王沟剖面２３层划分出５个生物地层带;Ⅰ带相当于榆社马会组;Ⅱ带与Ⅲ带相同庄组;Ⅳ带相当于麻则沟组;Ⅴ带为午城贡土底部。根据生物属种转换判定出４个主要生物事件发生时期,分别在５．８、３．６、．３０、２．４Ｍａ左右。每一个生物事件集中发生的时期指示生态环境的一次显著向干冷方向变化。     

甘肃灵台文王沟晚中新世一早更新世小哺乳动物

根据大量小哺乳动物化石在地层中的分布,将文王沟剖面２３层划分出５个生物地层带： Ｉ带相当于榆社马会组;ＩＩ带与Ⅲ带相当于高庄组; ＩＶ带相当于麻则沟组; Ｖ带为午城黄土底部。根据牛物属种转达换判定出 ４个主要生物事件发生时期,分别在 ５．８、３６、３．０、２．４Ｍａ左右。每一个生物事件集中发生的时期指示生态环境的一次显著向干冷方向变化。     

泥河湾盆地上新世小哺乳动物生物地层学及相关问题讨论

在泥河湾盆地稻地组与壶流河组、蔚县组命名剖面上分别筛洗小哺乳动物化石。其中花豹沟剖面选取 3个层位 ,发现小哺乳动物化石 1 0种 ;稻地剖面 6个层位 ,发现化石 2 5种。结合小哺乳动物化石组合 ,以及岩石地层追索对比 ,认为壶流河组与蔚县组从岩性上无法分开 ,应予合并 ,保留蔚县组 ;稻地组与蔚县组为同时期沉积 ,二者之间存在一定的相变关系 ,建议废止稻地组 ;仅保留蔚县组作为泥河湾组之下风成红黏土之上的岩石地层单位 ,其时代为中上新世晚期至晚上新世。     

晚中新世晚期土城子小哺乳动物组合及土城子动物群在内蒙古中部地区新近纪哺乳动物群序列中的位置（英文）

近百年来,在内蒙古中部地区发现了丰富的新近纪哺乳动物化石,命名和描述了10余个哺乳动物群,其时代跨越早中新世至早上新世。它们已经成为建立中国北方新近纪哺乳动物生物年代地层框架的重要依据。早在1959年中苏古生物联合考察过程中就已经发现土城子地区有丰富的哺乳动物化石,但这些化石以大–中型哺乳动物为主,缺乏小哺乳动物。土城子动物群的构成和其在中国北方新近纪哺乳动物年代地层框架中的位置长期以来不是特别明确。报道了在土城子新发现的6种小哺乳动物化石。根据Lophocricetus grabaui–Sinocricetus zdanskyi–Prosiphneus licenti–Hansdebruijnia pusilla–Moschus grandaevus的组合特点,认为土城子动物群的年代应该可以很好地约束在晚中新世(或者保德期)的晚期。土城子动物群明显比内蒙古的宝格达乌拉动物群要进步一些,与二登图动物群非常相似,时代上晚于前者,略早于后者。依据动物群整体面貌,推测在晚中新世晚期土城子地区存在森林和草原混合的环境。     

鄂西宜昌黄陵背斜地区寒武纪早期小壳化石新材料*

湖北宜昌地区寒武系下部小壳化石的研究集中于黄陵背斜东翼和南翼, 对西翼地区尚未有详细的报道。 作者在黄陵背斜西翼高岚河剖面灯影组天柱山段下部发现寒武纪纽芬兰世的小壳化石, 既包括扬子板块小壳化石第一生物带标准化石Anabarites trisulcatus, 同时也有Eohalobia diandongensis与Oelandiella korobkovi等第二生物带标志化石, 以及可能为第三生物带或更晚期化石分子的Paragloborilus tenuis等。该化石组合为多生物带的化石混生, 其层位可能相当于峡东地区(黄陵背斜南翼)的岩家河组顶部。在黄陵背斜南翼的滚石坳剖面岩家河组下部发现小壳化石Anabarites ternarius Missarzhevsky in Rozanov et al., 1969、Kaiyangites novilis Qian and Yin, 1984、 海绵骨针和藻类化石, 属于小壳化石第一生物带Anabarites trisulcatus–Protohertzina anabarica组合带。化石组合与沉积记录表明, 高岚河剖面与东翼如泰山庙地区具有相似的潮坪相沉积, 多发沉积间断, 导致不同生物带化石混生; 南翼滚石坳地区水体较深, 早期沉积间断不显著, 可以识别小壳化石第一组合带。上述新化石材料的发现, 为黄陵背斜周缘寒武系下部地层对比与生物古地理分析提供了新的数据。     

鄂西宜昌黄陵背斜地区寒武纪早期小壳化石新材料*

湖北宜昌地区寒武系下部小壳化石的研究集中于黄陵背斜东翼和南翼, 对西翼地区尚未有详细的报道。 作者在黄陵背斜西翼高岚河剖面灯影组天柱山段下部发现寒武纪纽芬兰世的小壳化石, 既包括扬子板块小壳化石第一生物带标准化石Anabarites trisulcatus, 同时也有Eohalobia diandongensis与Oelandiella korobkovi等第二生物带标志化石, 以及可能为第三生物带或更晚期化石分子的Paragloborilus tenuis等。该化石组合为多生物带的化石混生, 其层位可能相当于峡东地区(黄陵背斜南翼)的岩家河组顶部。在黄陵背斜南翼的滚石坳剖面岩家河组下部发现小壳化石Anabarites ternarius Missarzhevsky in Rozanov et al., 1969、Kaiyangites novilis Qian and Yin, 1984、 海绵骨针和藻类化石, 属于小壳化石第一生物带Anabarites trisulcatus–Protohertzina anabarica组合带。化石组合与沉积记录表明, 高岚河剖面与东翼如泰山庙地区具有相似的潮坪相沉积, 多发沉积间断, 导致不同生物带化石混生; 南翼滚石坳地区水体较深, 早期沉积间断不显著, 可以识别小壳化石第一组合带。上述新化石材料的发现, 为黄陵背斜周缘寒武系下部地层对比与生物古地理分析提供了新的数据。     

甘肃董湾晚新近纪地层及中新统/上新统界线

古地磁测年表明,甘肃董湾晚新近纪剖面代表了7.3～3.5 Ma间的连续风成古土壤堆积。在74.8 m厚的剖面上,发现了小哺乳动物化石层位40个,共产出小哺乳动物39种。根据小哺乳动物组合特点,董湾剖面可以划分出4个生物地层带,Ⅰ+Ⅱ带为晚中新世晚期,相当于保德期;Ⅲ+Ⅳ带为上新世早期,相当于榆社期早期。中新统/上新统界线(5.33 Ma)位于剖面距顶部35.5 m处,比以鼢鼠Mesosiphneus最早出现为标志的生物地层Ⅲ带的底界低2 m。由于榆社阶底界直接对应于中新统/上新统界线,该剖面因其良好的地层和生物条件可被推荐为榆社阶界线层型的候选剖面。     

小哺乳动物化石牙齿釉质碳、氧同位素测试方法简介及应用前景

探讨古环境和古气候变化与哺乳动物演化之间的关系是目前古生物学研究领域中的一个热点,而哺乳动物化石牙齿釉质的碳、氧同位素分析是恢复古环境和古气候的一个重要手段。以往的哺乳动物化石牙齿釉质稳定同位素分析多集中在大哺乳动物化石,这主要是受到技术手段的限制,所需的样品量较大所决定的。但最近几年随着激光和离子显微探针技术的应用,对小哺乳动物化石(如啮齿类和兔形类)的牙齿釉质碳、氧同位素的分析和应用日趋成熟和广泛。除了传统的化学处理方法之外,对小哺乳动物化石牙齿釉质碳、氧同位素的分析还有以下三种方法:1)激光剥蚀气相色谱/同位素比值质谱分析;2)直接激光氟化技术;3)离子显微探针技术(SHRIMPII)。这些技术需要的样品量少,对标本的破损小,准确度和精密度高,所以在小哺乳动物化石和一些珍贵标本(如古人类化石)的稳定同位素分析中起到了重要作用。相对于大哺乳动物化石,小哺乳动物化石数量多、演化速度快,更能反映多个层位长时间序列的古环境和气候变化;而且小哺乳动物通常没有长距离迁徙的行为,栖息地局限,所以更能准确反映化石埋藏地点的古环境和气候状况。     

内蒙古大庙中新世小哺乳动物化石埋藏学研究

捕食是小哺乳动物死亡最常见的原因,也导致被捕食动物遗骸发生明显改变.动物死亡后的风化、踩踏、搬运等过程也会改变动物的骨骼并影响到化石组合的形成.本文研究了内蒙古大庙三个中新世化石地点,时代从早中新世到晚中新世早期(约21～11.6 Ma).通过分析各小哺乳动物化石组合的沉积背景以及埋藏学特征识别化石埋藏的主要成因.结果显示出捕食是三个地点小哺乳动物化石埋藏的基本成因,而在两个年轻的地点中也有流水搬运与可能的踩踏因素的叠加.三个地点可能存在不一样的捕食者:早中新世地点以猫头鹰捕食为主,中、晚中新世地点则以日间活动的鸟类或哺乳类为主要捕食者.研究还显示小哺乳动物的系统发掘是可行的,在一定程度上可以减少采样过程中产生的破坏.     

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.     

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.     

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.     

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.     

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.     

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.