Deposition of trace substances via cloud interception on a coniferous forest at Kleiner Feldberg

A resistance model to calculate the deposition of cloud droplets on a coniferous forest and some improved parameterizations of the indispensable input parameters are described. The deposition model is adapted to the coniferous forest at the Kleiner Feldberg site and verified by the data of a drip water monitoring station below the forest canopy. The measurements of liqud water content, wind speed and trace substance compounds in cloud water of the Ground-based Cloud Experiment (GCE) at Kleiner Feldberg in 1990 are used to calculate the cloud water deposition fluxes and the deposition of trace substances via cloud water interception. The calculated deposition of trace substances via cloud water interceptions is three to six times higher than via rain during the experiment. On a long term data basis the yearly amount of cloud water deposition is 180 mm year^–1 at Kleiner Feldberg site (840 m a.s.l.) while the precipitation amount is 1030 mm year^–1. Due to higher trace substance concentrations in cloud water compared to rain the ionic deposition via cloud water interception and via precipitation were assessed to be of comparable magnitude.     

东北黑土区保护性耕作的发展现状与成效研究

东北黑土区承担着国家粮食安全“稳压器”的重要责任。然而,由于长期超负荷开发利用导致黑土日益退化,黑土资源的永续利用受到严重制约。理论与实践证明,保护性耕作是保护黑土地、推动黑土耕地质量和耕作效益绿色增长的发展模式。综述了保护性耕作的基本内涵及其在东北黑土区的发展现状与技术概况,从保护性耕作在土壤保持、保墒效益、结构改善、固碳培肥和土壤生物多样性增加、节本增效等方面系统评估了东北黑土区实施保护性耕作后的生态与经济效益,提出黑土区实施保护性耕作存在的问题与未来发展方向,以促进黑土地保护与利用协调发展、推动保护性耕作高质量跨越式发展。     

Meteorological excitation of the annual polar motion

Summary. Numerous studies have indicated that the annual term in the polar motion cannot be explained in any detail by meteorological/hydrological excitation and no reasonable alternative excitations have been put forward. Part of the problem has been that the hydrostatic adjustment of the oceans to the atmospheric pressure changes has traditionally been computed using the inverse barometer approach. This approach does not properly model the gravitational interaction between the atmosphere and oceans, and the inverse barometer theory is modified in this paper to account for this properly. The information necessary to compute the ocean tide and polar excitation caused by any change in the atmospheric pressure pattern is presented. The results of the application of this theory to two global atmospheric pressure data sets are examined and compared to results of other workers.
It is concluded that the atmosphere is observed well enough to answer the question of the annual excitation of polar motion and it is argued that the ground water excitation is the component with the largest error and remains the chief obstacle to the successful solution of this problem.     

河北平原水系密度与隐伏活动构造的关系

以1926年出版的比例尺为1：5万的顺直地形图作为基础图件，用地理信息系统技术对河北平原作水系密度计量分析，揭示隐伏在第四纪巨厚的沉积物之下活动构造的信息，研究结果证实水系线密度统计图与使用其它地球科学方法获得的成果，例如基底活动断块图，地貌类型图和第四纪厚度图都有很好的对应，特别与布格重力图对应更好，研究结果发现水系密度图与布格重力异常图在总体一致性较好的前提下，多处反向异常区均为近代强震发生的区域，提出这种地表水系密度统计研究的成果不仅可以揭示深部隐伏的活动构造，而且具有较明确的时间含义。     

Trace-element composition and zoning in clinopyroxene- and amphibole-group minerals: Implications for element partitioning and evolution of carbonatites

The present work is a first comprehensive study of the trace-element composition and zoning in clinopyroxene- and amphibole-group minerals from carbonatites, incorporating samples from 14 localities worldwide (Afrikanda, Aley, Alnö, Blue River, Eden Lake, Huayangchuan, Murun, Oka, Ozernaya Varaka, Ozernyi, Paint Lake, Pinghe, Prairie Lake, Turiy Mys). The new electron-microprobe data presented here significantly extend the known compositional range of clinopyroxenes and amphiboles from carbonatites. These data confirm that calcic and sodic clinopyroxenes from carbonatites are not separated by a compositional gap, instead forming an arcuate trend from nearly pure diopside through intermediate aegirine–augite compositions confined to a limited range of CaFeSi₂O₆ contents (15–45 mol%) to aegirine with < 25 mol% of CaMgSi₂O₆ and a negligible proportion of CaFeSi₂O₆. A large set of LA-ICPMS data shows that the clinopyroxenes of different composition are characterized by relatively low levels of Cr, Co and Ni (≤ 40 ppm) and manifold variations in the concentration of trivalent lithophile and some incompatible elements (1–150 ppm Sc, 26–6870 ppm V, 5–550 ppm Sr, 90–2360 ppm Zr, and nil to 150 ppm REE), recorded in some cases within a single crystal. The relative contribution of clinopyroxenes to the whole-rock Rb, Nb, Ta, Th and U budget is negligible. The major-element compositional range of amphiboles spans from alkali- and Al-poor members (tremolite) to Na–Al-rich Mg- or, less commonly, Fe-dominant members (magnesiohastingsite, hastingsite and pargasite), to calcic–sodic, sodic and potassic–sodic compositions intermediate between magnesio-ferrikatophorite, richterite, magnesioriebeckite, ferri-nyböite and (potassic-)magnesio-arfvedsonite. In comparison with the clinopyroxenes, the amphiboles contain similar levels of tetravalent high-field-strength elements (Ti, Zr and Hf) and compatible transition elements (Cr, Co and Ni), but are capable of incorporating much higher concentrations of Sc and incompatible elements (up to 500 ppm Sc, 43 ppm Rb, 1470 ppm Sr, 1230 ppm Ba, 80 ppm Pb, 1070 ppm REE, 140 ppm Y, and 180 ppm Nb). In some carbonatites, amphiboles contribute as much as 25% of the Zr + Hf, 15% of the Sr and 35% of the Rb + Ba whole-rock budget. Both clinopyroxenes and amphiboles may also host a significant share (~ 10%) of the bulk heavy-REE content. Our trace-element data show that the partitioning of REE between clinopyroxene (and, in some samples, amphibole) and the melt is clearly bimodal and requires a revision of the existing models assuming single-site REE partitioning. Clinopyroxenes and amphiboles from carbonatites exhibit a diversity of zoning patterns that cannot be explained exclusively on the basis of crystal chemistry and relative compatibility of different trace-element in these minerals. Paragenetic analysis indicates that in most cases, the observed zoning patterns develop in response to removal of selected trace elements by phases co-precipitating with clinopyroxene and amphibole (especially magnetite, fluorapatite, phlogopite and pyrochlore). With the exception of magnesiohastingsite–richterite sample from Afrikanda, the invariability of trace-element ratios in the majority of zoned clinopyroxene and amphibole crystals implies that fluids are not involved in the development of zoning in these minerals. The implications of the new trace-element data for mineral exploration targeting REE, Nb and other types of carbonatite-hosted rare-metal mineralization are discussed.