地面风对瓦里关山大气CH4本底浓度的影响分析

使用1994年7月至1996年12月大气CH₄和地面风现场连续观测资料，分析了瓦里关全球大气本底基准站（36°17′N, 100°54′E，海拔3816 m）地面风变化对大气CH₄本底浓度的影响。结果表明，水平风向、风速和垂直风向、风速的变化对大气CH₄观测值的影响在春、夏、秋、冬季有明显不同，水平风向NE—ENE—E为CH₄测量最主要的局地影响非本底扇区，静风及水平风速大于10 m/s、垂直风速大于±1 m/s对观测结果都有较大影响；由的统计平均还给出了此段期间瓦里关大气CH₄在不同季节的浓度分布范围和日变化类型，并分析了可能成因；将地面风数据作为大气CH₄本底资料的过滤因子之一，提出了适用于不同使用目的和要求的我国内陆高原大气CH₄本底数据筛选方法，本底数据留存率约为原始资料量的50%。     

多普勒雷达资料4DVAR同化反演的模拟研究

利用Sun等建立的同化模式和四维变分同化方法对多普勒雷达资料反演大气风场、热力场和微物理场进行了模拟试验研究.反演的基本思路是将4DVAR同化方法应用到三维云模式,定义价值函数表征雷达资料与模式预报结果之间的差别,通过极小化价值函数得到反演场,价值函数相对模式控制变量的梯度由伴随模式求取.试验结果表明,4DVAR同化技术能够从单(双)多普勒雷达资料反演大气三维风场、热力场和微物理场.各个变量反演精度高低与同化过程中变量受约束的大小程度呈正相关.速度场和雨水场反演精度较高,温度场、云水和水汽的反演精度次之,温度场的准确反演需要较长的同化时间.价值函数中加入背景场,哪怕是单点探空给出的平均场信息也有利于提高反演精度.在采用单部多普勒雷达资料进行反演时,速度场的反演误差较大.反演区相对雷达站的位置变化对速度场反演结果有一定的影响,而对其他变量的反演影响很小.两个时次的雷达观测资料基本足够提供反演所需的时间演变信息,同化更多时次的雷达资料,反演效果改进很小.雷达观测资料的缺值会显著降低同化效果,甚至可能导致同化失败,引入背景场可以改善这一状况.4DVAR同化技术对于雷达观测资料误差不太敏感.利用双多普勒雷达合成风场提供水平风场边界条件是比较准确可靠的.在反演主体离边界较远时,VAD风场也基本可用作水平风场边界条件.微物理场的反演对模式中的微物理参数化方案较敏感.     

塔里木河南岸地下淡水资源分布特征及成因分析--以哈得4油田水源地为例

塔里木河南岸地下水资源，卡要为受塔里水河控制的具有高矿化背景的地下水，在塔里木河洪水的淡化影响下，形成了一定范围的地下水淡化带．这种淡化水对油田供水具有战略意义，在一定程度上制约着油田建设的发展．通过对塔埋木河南岸地下淡水资源的分布特征与成因分析．为塔河南岸地下淡水资源的合理开发与利用指明了方向．     

影响C4草本植物C/N比值变化的因素与土壤有机C积累的关系

文章对采自贵州从低海拔的东部到高海拔的西部且大致平行的石灰岩和砂岩两地带均生长的3种C₄草本植物,即巴茅(Miscanthusfloridulus)、白茅(Imperatacylindrica)和类芦(Neyraudiareynaudiana),以及相对应的土壤表层样品,进行了营养元素和C同位素组成分析;研究营养元素含量随着海拔的不同而出现的变化趋势,以及这些元素之间的相互协变作用,尤其是Ca和N之间的相互协变作用对植物的N含量、C/N比值和^δ13C值的影响,以了解植物的C/N比值(指示植物残留物质量的一种标志)与土壤有机C积累的关系。研究结果表明,植物的N含量和^δ13C值具有随海拔的上升而显著增大趋势,而植物的C/N比值在砂岩地区虽有减小的趋势,在石灰岩地带则没有。对所研究的C4草本植物来说,在土壤pH值为5.8的中性条件下显示出Ca的最大吸收,因此,Ca与其他营养元素之间的协变模式在两种土壤类型中表现出相反的倾向,并存在土壤交换性Ca的边界浓度:当土壤可交换性Ca的含量为2.24mg/g,相应土壤的pH值在5.8以下时,随着土壤可交换性Ca浓度的增大,植物的N含量上升,而植物的C/N比值会显著降低;当Ca在边界浓度以上时,随着土壤可交换性Ca浓度的增大,植物的N含量下降,而植物的C/N比值有增加的趋势。由此可见,植物残留物的N含量和C/N比值受Ca元素含量的相     

Methane-rich fluid inclusions in skarn near the giant REE–Nb–Fe deposit at Bayan Obo, Northern China

We report fluid inclusion data for skarn, formed at the contact between Hercynian granitoids and dolomite of the Proterozoic Bayan Obo Group, in the vicinity of Bayan Obo REE–Nb–Fe deposit, Inner Mongolia, China. Three types of fluid inclusions are identified: two-phase CH₄-rich, three-phase liquid–vapour–solid and two-phase aqueous inclusions. Using microthermometry and laser Raman microprobe analysis to calculate isochores for CH₄-bearing inclusions, we estimate fluid trapping conditions at T=280 to 344 °C and P<1 to 2.3 kbar. Such conditions are compatible with formation of CH₄ inclusions as a result of reaction between graphite in the country rocks (black slate sequence) and fluids derived from magma. The lack of carbonaceous material in the inclusions supports the hypothesis that CH₄ was generated during fluid migration rather than by in situ reaction. In contrast to the skarn, and despite the fact that similar graphite-bearing slates are found in the host rocks, no CH₄-bearing inclusions have been so far reported from Bayan Obo REE ores. We therefore conclude that the skarn-forming fluids in the contact aureole of the Hercynian granitoids were not involved at any stage in the formation of the Bayan Obo deposit.     

洛川黄土剖面中矿物固定态铵的分布

对洛川黄土中的固定铵进行了初步分析。结果表明,在所测定的黄土古土壤层中,固定铵态氮含量在130-1之间变化。黄土中的固定铵态氮含量明显低于古土壤。13万a以来洛川黄土剖面中固定铵的分布呈～210现三次大的低高值的振荡特征,即末次间冰期S1古土壤中固定铵态氮含量最高,其次为冰后期的S0古土壤层,末次冰期形成的马兰黄土中固定铵态氮含量最低;在马兰黄土中同样体现出三次小的低高值的波动特征。黄土与μm组分的分布具有相似性,这些特征反映了洛川黄土中固定铵态氮的含量变化与气互层的古土壤中固定态铵的分布与黄土高原区气候的冷暖变化有较好的一致性,并且13万a以来洛川黄土剖面中固定铵的分布与磁化率和<2候条件有紧密的联系,揭示了黄土中固定铵的变化在一定程度上能指示黄土高原区古气候的演变。     

Continuous Multi‐probe Measurements in Fastflowing Waters Using a Hydrographic Slot

Taking continuous spatiotemporal in situ measurements with multi‐probes in fast‐flowing waters/rivers can be problematic because the sensors may be damaged by high shear forces and flotsam. To protect the multi‐probe and to enable easy access for the maintenance and calibration of the sensors, a special multi‐probe holder fixed in a hydrographic slot was developed. The validation of the probe system revealed a “memory effect” at short time scales (< 10 s) within sharp gradients caused by the overflow container of the multi‐probe rack keeping the sensors submerged in the sample water. Continuously recorded data (conductivity, temperature, pH, oxygen concentration and saturation, as well as in vivo fluorescence of chlorophyll‐a) from a research cruise on board the RV ALBIS along the river Elbe (river km 309) and entering the river Saale are presented. This river stretch upstream of the city of Magdeburg to the mouth of the Saale tributary was found to have a complex physicochemical character, which is attributable to the long mixing process of water from the river Saale and the river Elbe.     

Sorption of carbon dioxide–methane mixtures

The paper reports the results of experiments concerning the sorption/desorption processes, observed under laboratory conditions, in two types of coal extracted from operational coal-mines in Poland, using CH₄ and CO₂ to observe their relative inter-reaction with the coal samples when introduced in varying proportions and conditions. Numerous studies concerning the sorption/desorption phenomena have described the operational mechanisms and the relationship of mine gases to the organically-created coal-body in mines. The differences in the behaviour of certain gases is twofold: firstly the essentially different characteristics of CO₂ and CH₄, and secondly the structure of the coal-bed itself: its degree of metamorphism and content of macerals. From the results yielded, it was observed that the divergence of the isotherms of sorption of CH₄ and other gases in comparison with the isotherms of sorption of CO₂ and a CO₂/CH₄ mixture differed and that the curve on the sorption isotherm was more clearly distinct after the introduction of CO₂ molecules to the system: coal with a higher degree of metamorphism—CH₄, which is closely related to the rigidity of the structure according to the level of metamorphism. Since coals with higher carbon content exhibit lower molecular bonding than low-carbonised coals, the characteristic feature of the bonds in the first case is their mobility. Knowledge of the physical and chemical properties of hard coals, as well as their interaction with mining gases, is of great use in solving problems concerned with the extraction of methane from mines or its storage in goafs.     

Environmental significance of C/C and O/O ratios of modern land-snail shells from the southern great plains of North America

¹³C/¹²C and ¹⁸O/¹⁶O ratios of aragonite shells of modern land snails from the southern Great Plains of North America were measured for samples from twelve localities in a narrow east-west corridor that extended from the Flint Hills in North Central Oklahoma to the foothills of the Sangre de Cristo Mountains in Northern New Mexico, USA. Across the study area, shell δ¹⁸O values (PDB scale) ranged from −4.1‰ to 1.2‰, while δ¹³C values ranged from −13.2‰ to 0.0‰. δ¹⁸O values of the shell aragonite were predicted with a published, steady state, evaporative flux balance model. The predicted values differed (with one exception) by less than 1‰ from locality averages of measured δ¹⁸O values. This similarity suggests that relative humidity at the time of snail activity is an important control on the δ¹⁸O values of the aragonite and emphasizes the seasonal nature of the climatic information preserved in the shells. Correlated δ¹³C values of coexisting Vallonia and Gastrocopta suggest similar feeding habits and imply that these genera can provide information on variations in southern Great Plains plant ecology. Although there is considerable scatter, multispecies, transect average δ¹³C values of the modern aragonite shells are related to variations in the type of photosynthesis (i.e., C₃, C₄) in the local plant communities. The results of this study emphasize the desirability of obtaining isotope ratios representing averages of many shells in a locale to reduce possible biases associated with local variations among individuals, species, etc., and thus better represent the “neighborhood” scale temporal and/or spatial environmental variations of interest in studies of modern and ancient systems.