美国NCEP/NCAR全球再分析资料及其初步分析

对美国国家环境预测中心（ＮＣＥＰ）及国家大气研究中心（ＮＣＡＲ）的４０年全球再分析资料在中国应用的可信度进行了初步分析,其中包括温、压、风、湿、降雨量、地面辐射、地面感热、地面蒸发潜热及青藏高原地面热源等。除降水量再分析资料与气候资料的比较属同一时段外,其余均属非同一时段比较。两者基本特征和分布形势一致,再分析资料比较合理。     

Economic Development and Emission Control over the Long Term: The ICLIPS Aggregated Economic Model

In integrated assessments of climate change, greenhouse-gasemissions and climate change impacts provide the linkages betweenthe world economy and the climate system. Key climatic processesoperate at the scales of centuries. This requires highlyaggregated models for portraying the dynamics of the economicsystem. An extended Ramsey-type optimal growth model is presentedas the appropriate tool to be integrated with a reduced-formclimate model in the ICLIPS integrated assessment. Theeleven-region model of the world economy involves exogenouspopulation and endogenous investment dynamics with productivityprogress based on a technological diffusion model. World regionsare linked via intertemporal trade flows of the compositeconsumption/investment good, capital mobility, and emission permittrading. Coupled with the ICLIPS Climate Model, the AggregatedEconomic Model can determine corridors of permitted long-termcarbon emission paths or, as primarily discussed in this paper,specific cost-effective emission trajectories. The sensitivity ofmitigation costs to externally specified climate change/impactconstraints and to assumptions about non-CO₂ greenhouse-gasemissions is also discussed.     

A study of ozone in the Colorado mountains

The seasonal and diurnal variations of ozone mixing ratios have been observed at Niwot Ridge. Colorado. The ozone mixing ratios have been correlated with the NO _x (NO+NO₂) mixing ratios measured concurrently at the site. The seasonal and diurnal variations in O₃ can be reasonably well understood by considering photochemistry and transport. In the winter there is no apparent systematic diurnal variation in the O₃ mixing ratio because there is little diurnal change of transport and a slow photochemistry. In the summer, the O₃ levels at the site are suppressed at night due to the presence of a nocturnal inversion layer that isolated ozone near the surface, where it is destroyed. Ozone is observed to increase in the summer during the day. The increases in ozone correlate with increasing NO _x levels, as well as with the levels of other compounds of anthropogenic origin. We interpret this correlation as in-situ or in-transit photochemical production of ozone from these precursors that are transported to our site. The levels of ozone recorded approach 100 ppbv at NO _x mixing ratios of approximately 3 ppbv. Calculations made using a simple clean tropospheric chemical model are consistent with the NO _x -related trend observed for the daytime ozone mixing ratio. However, the chemistry, which does not include nonmethane hydrocarbon photochemistry, underestimates the observed O₃ production.     

XMCD at Fe L<Subscript>2,3</Subscript> edges,Fe and S K edges on Fe<Subscript>7</Subscript>S<Subscript>8</Subscript>

Pyrrhotite (Fe₇S₈) is a natural iron sulphide that can participate in rock magnetisation. Its electronic structure is not yet surely described. X-ray magnetic circular dichroism (XMCD) at Fe L_2,3 edges on Fe₇S₈, coupled with multiplet calculations, shows that iron is present only as Fe²⁺ in this magnetic iron sulphide. It reveals a strong magnetic orbital moment. XMCD at Fe and S K edges shows the quite strong polarization of both Fe and S in Fe₇S₈.     

Bacterial genesis of calcium phosphates in human organism and nature

Comparison of natural marine (nodular and granular) carbonate-apatites and pathogenic mineral structures formed in human cardiac valves by methods of scanning electron and high-resolution transmission microscopy revealed common morphological features corresponding to the bacterial origin of calcium phosphates. These features may be considered typomorphic ones regardless of their formation environments (in vivo or in nature).     

Origin of Minette by Mixing of Lamproite and Dacite Magmas in Veliki Majdan, Serbia

Composite dykes consisting of leucominette and dacite as wellas discrete dykes and flows of minette and lamproite composition,occur in the Veliki Majdan area, western Serbia. This area ispart of the Serbian Tertiary magmatic province, which consistsof numerous small occurrences of ultrapotassic igneous rocks.The composite dykes have leucominette margins (up to 150 cmthick) enclosing a central part of dacite up to 100 m in width.Between these two lithologies, a decimetre-sized transitionzone may occur. Petrography, mineral chemistry and bulk-rockgeochemistry, including Sr, Nd and Pb isotopes, provide evidencethat the minettes and leucominettes formed by hybridizationbetween a felsic magma similar in composition to dacite anda mantle-derived lamproitic magma. The leucominettes and minettescontain all phenocryst types (biotite, plagioclase, quartz)present in the dacites, but in partly resorbed and reacted form.The mica displays a great diversity of resorption textures asa result of partial dissolution, incipient melting and phlogopitization,suggesting superheating of the felsic melt during hybridization;the mineral modes and mineral compositions of the leucominettesand minettes resemble those in the lamproites. A model for themodification of lamproite melt towards minette is presentedin which minette is formed by mixing of lamproite and <30%felsic magma. The lack of any significant correlation betweenPb isotopic ratios and some of the ‘mixing-indices’(SiO₂, Zr, Zr/Nb, ¹⁴³Nd/¹⁴⁴Nd_i) recognized in the hybridizationmodel for the Veliki Majdan dykes may be a result of similarityof the Pb-isotopic signature in the two end-members. Highlyphlogopitized biotite xenocrysts in the minettes are ascribedto the retention of volatile components after magma mixing andcrystallization of a new generation of phlogopite from the hybridizedmagma. The magma-mixing model explains the reverse zoning andresorption features of phlogopite macrocrysts commonly recognizedin calcalkaline lamprophyres elsewhere. Therefore, this mixingmechanism may be globally applicable for the origin of minettesassociated with calcalkaline granitic plutonism in post-orogenicsettings. KEY WORDS: Serbia; lamproites; micas; phlogopitization; calcalkaline lamprophyres; superheating; magma mixing     

The Removal of Dissolved Metals by Hydroxysulphate Precipitates during Oxidation and Neutralization of Acid Mine Waters, Iberian Pyrite Belt

This study examines the removal of dissolved metals during the oxidation and neutralization of five acid mine drainage (AMD) waters from La Zarza, Lomero, Esperanza, Corta Atalaya and Poderosa mines (Iberian Pyrite Belt, Huelva, Spain). These waters were selected to cover the spectrum of pH (2.2–3.5) and chemical composition (e.g., 319–2,103 mg/L Fe; 2.85–33.3 g/L SO₄⁼) of the IPB mine waters. The experiments were conducted in the laboratory to simulate the geochemical evolution previously recognized in the field. This evolution includes two stages: (1) oxidation of dissolved Fe(II) followed by hydrolysis and precipitation of Fe(III), and (2) progressive pH increase during mixing with fresh waters. Fe(III) precipitates at pH < 3.5 (stages 1 and 2) in the form of schwertmannite, whereas Al precipitates during stage 2 at pH 5.0 in the form of several hydroxysulphates of variable composition (hydrobasaluminite, basaluminite, aluminite). During these stages, trace elements are totally or partially sorbed and/or coprecipitated at different rates depending basically on pH, as well as on the activity of the SO₄⁼ anion (which determines the speciation of metals). The general trend for the metals which are chiefly present as aqueous free cations (Pb²⁺, Zn²⁺, Cu²⁺, Cd²⁺, Mn²⁺, Co²⁺, Ni²⁺) is a progressive sorption at increasing pH. On the other hand, As and V (mainly present as anionic species) are completely scavenged during the oxidation stage at pH < 3.5. In waters with high activities (> 10⁻¹) of the SO ₄⁼ ion, some elements like Al, Zn, Cd, Pb and U can also form anionic bisulphate complexes and be significantly sorbed at pH < 5. The removal rates at pH 7.0 range from around 100% for As, V, Cu and U, and 60–80% for Pb, to less than 20% for Zn, Co, Ni and Mn. These processes of metal removal represent a significant mechanism of natural attenuation in the IPB.     

Interaction of crustal and mantle materials,sources of trace elements during the formation and evolution of Early Paleozoic Li-rich granite-pegmatite systems in southeastern Tuva

We present new data on the age, composition, and environments of formation of granites of the Kystarys complex and the associated Li-rich rare-element pegmatites of the South Sangilen pegmatite belt including the large Tastyg lithium deposit. It has been established that they formed during the Early Paleozoic collisional orogeny in the Tuva-Mongolian massif at the Cambrian-Ordovician boundary. The granites of the Kystarys complex are moderately alkaline high-K rocks and are enriched in Zr, Nb, Y, and REE; therefore, they are classified as postcollisional, transitional to within-plate (A-type). The spodumene pegmatites of the South Sangilen pegmatite belt are similar to the above granites in age and isotopic and geochemical parameters, which suggests a paragenetic relationship between these rocks. Pegmatites form several pegmatite fields within the belt, which differ in trace-element signatures. In addition to predominant Li, Cs, and Ta, specific to all spodumene pegmatites (LCT family), pegmatites of two fields have high contents of Nb, Y, REE, and Zr, which are indicator elements of NYF family pegmatites. It has been established that the formation of spodumene pegmatites with combined LCT-NYF geochemical signatures was preceded by the intrusion of dikes of monzogabbro with the geochemical characteristics of OIB and of alkali aegirine granites and by the formation of associated metasomatites enriched in Zr, Nb, Y, and REE. Based on the geological, mineralogical, and geochemical data, we substantiate the hypothesis of the formation of Li-bearing granite-pegmatite melts from a mixed source resulted from the influence of fluids of an alkaline igneous complex of mantle genesis on the crustal protolith.     

苏丹穆格莱德盆地福拉凹陷油气成藏特征及勘探启示

福拉凹陷下白垩统Abu Gabra组发育有湖相好—极好烃源岩,但热演化程度低、成藏主控因素不确定,勘探潜力不明。通过地层层序划分、构造分析、沉积相分析,认为张剪性区域构造背景控制福拉凹陷的构造与沉积发育,下白垩统Abu Gabra组发育有一定规模有效生烃凹陷,可形成Abu Gabra组烃源岩层,Abu Gabra组自储自盖,Bentiu组储、Aradeiba组盖及Aradeiba组自储自盖等3套生储盖组合,其中第二套储盖组合为该凹陷不同于六区其他凹陷的良好储盖组合。紧邻生烃凹陷、继承性发育的构造带,如中部滚动背斜—断鼻、南部次凹西缘断鼻、南部断阶带断鼻、北部次凹东缘断鼻等构造带是有利的成藏带。继承性发育的Fula1号滚动背斜、Fula2号断鼻构造具有多套储盖组合,勘探风险低,为有利的勘探目标。这些认识为福拉凹陷油气勘探提供了科学依据,且其研究方法及思路也为新区油气勘探提供良好的借鉴。     

Origin and evolution of the Steamboat Springs siliceous sinter deposit, Nevada, U.S.A.

Siliceous hot spring deposits from Steamboat Springs, Nevada, U.S.A., record a complex interplay of multiple, changing, primary environmental conditions, fluid overprinting and diagenesis. Consequently these deposits reflect dynamic geologic and geothermal processes. Two surface sinters were examined—the high terrace, and the distal apron-slope, as well as 13.11 m (43 ft) of core material from drill hole SNLG 87-29. The high terrace sinter consists of vitreous and massive-mottled silica horizons, while the distal deposit and core comprise dominantly porous, indurated fragmental sinters. Collectively, the three sinter deposits archive a complete sequence of silica phase diagenetic minerals from opal-A to quartz. X-ray powder diffraction analyses and infrared spectroscopy of the sinters indicate that the distal apron-slope consists of opal-A and opal-A/CT mineralogy; the core yielded opal-A/CT and opal-CT with minor opal-A; and the high terrace constitutes opal-C, moganite, and quartz. Mineralogical maturation of the deposit produced alternating nano–micro–nano-sized silica particle changes. Based on filament diameters of microbial fossils preserved within the sinter, discharging thermal outflows fluctuated between low-temperatures (< 35 °C, coarse filaments) and mid-temperatures ( 35–60 °C, fine filaments). Despite transformation to quartz, primary coarse and fine filaments were preserved in the high terrace sinter. AMS ¹⁴C dating of pollen from three horizons within core SNLG 87-29, from depths of 8.13 to 8.21 m (26′8″ to 26′11″), 10.13 to 10.21 m (33′3″ to 33′6″), and 14.81 to 14.88 m (48′7″ to 48′10″), yielded dates of 8684 ± 64 years, 11,493 ± 70 years and 6283 ±60 years, respectively. In the upper section of the core, the stratigraphically out-of-sequence age likely reflects physical mixing of younger sinter with quartzose sinter fragments derived from the high terrace. Within single horizons, mineralogical and morphological components of the sinter matrix were spatially patchy. Overall, the deposit was modified by sub-surface flow of alkali-chloride thermal fluids depositing a second generation of silica, and periodically, by acidic steam condensate formed during periods when the water table was low. Local faulting produced considerable fracturing of the sinter. Hence, the Steamboat Springs sinter experienced a complex history of primary and secondary hydrothermal, geologic and diagenetic events, and their inter-relationships and effects are locked within the physical, chemical and biological signatures of the deposit.