利用新编依巴谷天体测量资料研究银河系运动

根据最近发表的新编依巴谷星表数据,重新研究了经典造父变星周光关系零点问题.利用运动学模型对自行数据和视向速度分别拟合奥尔特常数及本地静止标准的旋转速度,得到太阳的银心距R0=8.0±0.8kpc.从太阳附近的旋转曲线,发现银河系盘的引力势具有弱椭圆分布的迹象.通过-个简单的非对称模型,得到太阳附近盘引力势的椭率e(R0)=0.067±0.036,其短轴指向φb=32°±15°.     

Observational Study of a Peculiar Solar Limb Event Occurred on 11 January 2002

On 11 January 2002, using the Multi-channel Infrared Solar Spectrograph (MISS) at the Purple Mountain Observatory (PMO), we obtained Hα, Ca ii 8542 Å and He i 10?830 Å spectra and slit-jaw Hα images of a peculiar solar limb event. A close resemblance of its intensity to that of a small flare and the GOES X-ray flux indicates that it was an active prominence. However, its morphological evolution and velocity variation were different from general typical active prominences, such as limb flares, post-flare loops, surges and sprays. It started with the ejection of material from the flare site. In the early phase, the ejecta was as bright as a limb flare and kept rising until reaching the height of (8????10)×10⁴ km at an almost constant velocity of 91.7 km? s ^?1 with its lower part always connected to the solar surface. EUV images in 195 Å show similar structure as in the Hα line, indicating the coexistence of plasmas with temperatures differing by more than two orders of magnitude. Later some material started to fall back to another bright area on the solar surface. The falling material did not show the collimated structure of surges or the arc structure of flaring arches. A red-shift velocity of more than 200 km? s ^?1 was detected in a bright point close to the outer edge of the closed loop system formed later, which dispersed in a few minutes and became a part of the newly formed large loop. The ejected material did not leave the sun, indicating that the magnetic reconnection was not sufficient to remove the overlying field lines during the process. The spectral line profiles showed large widths and variable velocities, and therefore the line-pair method is not applicable to this event for the estimation of physical parameters.     

爱因斯坦环及其星系团环境

该文研究了以星系作为透镜体产生的切向弧(即"爱因斯坦环")的强引力透镜现象,并对该领域近年来的观测和研究作了总结.对形成这些强引力透镜"环"的星系所进行的研究表明,其附近存在的质量所产生的会聚和剪切对透镜的质量分布模型非常敏感.在大视场巡天中找到的这种爱因斯坦环的数目相当多,大约是每平方度10个,其中"强引力透镜巡天"(Strong LensingLegacy Survey,SL2S)提供了大量处于星系团视场中的由椭圆星系产生的爱因斯坦环样本.系统地研究星系团外围存在的爱因斯坦环,一方面可以理解星系团环境对爱因斯坦环的影响,另一方面可以利用它们来探测星系团的物质分布,并进而对冷暗物质宇宙学提供新的探测方法.     

利用窄线宽激光测量锶原子束速率分布

利用多普勒频移效应,通过线宽2MHz窄线宽激光与锶原子束在大角度作用下的荧光信号分析,测量了锶原子束速率分布。比较和分析表明,理论结果与实验结果符合较好。     

New insights into the origin of perylene in geological samples

The origin of the polycyclic aromatic hydrocarbon (PAH) perylene in sediments and petroleum has been a matter of continued debate. Reported to occur in Phanerozoic organic matter (OM), fossil crinoids and tropical termite mounds, its mechanism of formation remains unclear. While a combustion source can be excluded, structural similarities to perylene quinone-like components present in e.g. fungi, plants, crinoids and insects, potentially suggest a product-precursor relationship. Here, we report perylene concentrations, ¹³C/¹²C, and D/H ratios from a Holocene sediment profile from the Qingpu trench, Yangtze Delta region, China. Perylene concentrations differ from those of pyrogenic PAHs, and rise to prominence in a stratigraphic interval that was dominated by woody vegetation as determined by palynology including fungal spores. In this zone, perylene concentrations exhibit an inverse relationship to the lignin marker guaiacol, D/H ratios between −284‰ and −317‰, similar to the methoxy groups in lignin, as well as co-variation with spores from wood-degrading fungi. ¹³C/¹²C of perylene differs from that of land plant wax alkanes and falls in the fractionation range expected for saprophytic fungi that utilise lignin, which is isotopically lighter than cellulose and whole wood. During progressive lignin degradation, the relative carbon isotopic ratio of the perylene decreases. We therefore hypothesise a relationship of perylene to the activity of wood-degrading fungi. To support our hypothesis, we analysed a wide range of Phanerozoic sediments and oils, and found perylene to generally be present in subordinate amounts before the evolutionary rise of vascular plants, and to be generally absent from marine-sourced oils, few exceptions being attributed perhaps to a contribution of marine and/or terrestrial-derived fungi, anoxia (especially under marine conditions) and/or contamination of core material by fungi. A series of low-molecular-weight aromatic quinones bearing the perylene-backbone were detected in Devonian and Cretaceous sediments, potentially representing precursor components to perylene.     

Distribution and significance of novel low molecular weight sterenes in an immature evaporitic sediment from the Jinxian Sag,North China

An unusual series of C₂₂–C₂₇ monounsaturated sterenes and C₂₄–C₃₀ tetracyclic terpanes (17,21-secohopanes) were detected in relatively high concentrations in an immature evaporitic marl sediment of the Jinxian Sag, Bohai Bay Basin, North China. The site of unsaturation in these novel sterenes is assigned tentatively to the D ring on the basis of mass spectral interpretation, which also distinguishes them from reported unsaturated sterenes. Other hydrocarbon biomarker or stable isotope characteristics are indicative of microbial (e.g. methyl hopanes), phytoplankton or higher plant (depleted δ¹³C values of isoprenoids and hopanes) inputs and an anoxic carbonate depositional environment (hexacyclic hopanes; tetracyclic terpanes). The hydrocarbon composition showed no obvious biodegradation and the relatively high concentration of unsaturated terpenoids (e.g. gammacerene) and low values of other established maturity parameters (T_s/T_m = 0.23; R_o = 0.44%; T_max = 417 °C), are consistent with sediments of low maturity. The novel, low molecular weight sterenes and the tetracyclic terpanes may be early diagenetic products of microbial sources in a carbonate environment.     

空气滤膜采集大气浮尘样品中多元素的测定

用氢氟酸-盐酸-硝酸-高氯酸体系对空气滤膜上附着的浮尘样品进行分解,电感耦合等离子体发射光谱法、电感耦合等离子体质谱法同时测定溶液中15个主量和微量元素铁、铜、锌、镍、镧、铈、锂、锰、铬、镉、钴、铅、钍、铊、铀。将国家一级标准物质模拟浮尘样品加入空白滤膜进行测定,结果与标准值相符。各元素4次测定结果的相对标准偏差(RSD)小于5%。     

高效液相色谱-紫外光谱分析氢醌-双(β-羟乙基)醚

建立了高效液相色谱-紫外光谱法测定聚氨酯扩链剂氢醌-双(β-羟乙基)醚(HQEE)工业品中HQEE主含量和对苯二酚残留的方法。在氰基柱上,以甲醇-水-1%乙酸溶液(体积比10∶50∶40)为流动相,流速1.0 mL/min时,HQEE、对苯二酚及其他相关杂质得到良好分离,紫外光谱285 nm检测。方法简便、快捷,结果准确可靠,在工业生产中可有效地指导HQEE合成过程的质量控制。     

电感耦合等离子体质谱法测定岩石样品中的锆铌铪钽两种预处理方法的比较

研究了微波消解酸溶和过氧化钠碱熔两种测定岩石样品中锆、铌、铪、钽前处理方法,利用电感耦合等离子体质谱法进行测定。对所选用不同种类的岩石国家标准物质样品进行了条件实验,结果表明:采用过氧化钠碱熔法处理岩石样品后,锆、铌、铪、钽的测量值准确度高,且相对标准偏差(RSD,n=10)小于6%,该方法更适用于岩石样品中锆、铌、铪、钽的测定。     

煤炭资源勘探技术框架重构

在我国第一能源-煤炭资源持续紧缺的形势下,50%的深部资源开发正面临许多新的地质勘探问题.矿井物探技术进步有力的推动着资源开发勘探方法的改变,在井下巷道中对下纽资源的纵深向勘探和水平向勘探技术的成熟,促使技术框架重构.在一井一面高强度开采的煤矿生产组织新模式下,采空区下深部资源勘探、安全地质条件评价和治理、基于"3S"的递推地质管理技术等是老矿区深部资源勘探急需的支撑技术,矿井与地面结合必然是煤炭资源勘探技术发展的方向.