A study of the diurnal variation in the thermosphere as derived by satellite drag     

L.G. Jacchia  I.G. Campbell  J.W. Slowey 《Planetary and Space Science》1973,21(11):1825-1834

An analysis was performed on 29,574 densities derived from the drag of 10 satellites to determine simultaneously the parameters of the solar-activity effect in the thermosphere on the one hand, and the amplitude and shape of the diurnal-variation curve on the other. This paper reports on the study of the diurnal variation only.Although a considerable amount of smoothing is inherent in the drag method, it seemed useful to see whether we could detect any change in the shape of the diurnal-variation curve with height, latitude and solar activity. None was detected: the curve remains remarkably stable, symmetric, with a maximum at 14 hr 20 min L.S.T. and a minimum at 2 hr 20 min L.S.T. A systematic variation of the temperature range with height is observed when static models are used to derive it.  相似文献   

Transformations of mercury, iron, and sulfur during the reductive dissolution of iron oxyhydroxide by sulfide   总被引：1，自引：0，他引：1  

Aaron J. Slowey  Gordon E. Brown Jr. 《Geochimica et cosmochimica acta》2007,71(4):877-894

Methylmercury can accumulate in fish to concentrations unhealthy for humans and other predatory mammals. Most sources of mercury (Hg) emit inorganic species to the environment. Therefore, ecological harm occurs when inorganic Hg is converted to methylmercury. Sulfate- and iron-reducing bacteria (SRB and FeRB) methylate Hg, but the effects of processes involving oxidized and reduced forms of sulfur and iron on the reactivity of Hg, including the propensity of inorganic Hg to be methylated, are poorly understood. Under abiotic conditions, using a laboratory flow reactor, bisulfide (HS⁻) was added at 40 to 250 μM h⁻¹ to 5 g L⁻¹ goethite (α-FeOOH) suspensions to which Hg(II) was adsorbed (30-100 nmol m⁻²) at pH 7.5. Dissolved Hg initially decreased from 10³ or 10⁴ nM (depending on initial conditions) to 10⁻¹ nM, during which the concentration of Hg(II) adsorbed to goethite decreased by 80% and metacinnabar (β-HgS_(s)) formed, based on identification using Hg L_III-edge extended X-ray absorption fine structure (EXAFS) spectroscopic analysis. The apparent coordination of oxygens surrounding Hg(II), measured with EXAFS spectroscopy, increased during one flow experiment, suggesting desorption of monodentate-bound Hg(II) while bidentate-bound Hg(II) persisted on the goethite surface. Further sulfidation increased dissolved Hg concentrations by one to two orders of magnitude (0.5 to 10 nM or 30 nM), suggesting that byproducts of bisulfide oxidation and Fe(III) reduction, primarily polysulfide and potentially Fe(II), enhanced the dissolution of β-HgS_(s) and/or desorption of Hg(II). Rapid accumulation of Fe(II) in the solid phase (up to 40 μmol g⁻¹) coincided with faster elevation of dissolved Hg concentrations. Fe(II) served as a proxy for elemental sulfur [S(0)], as S(0) was the dominant bisulfide oxidation product coupled to Fe(III) reduction, based on sulfur K-edge X-ray absorption near edge structure (XANES) spectroscopy. In one experiment, dissolved Hg concentrations tracked those of all sulfide species [S(-II)]. These results suggest that S(-II) reacted with S(0) to form polysulfide, which then caused the dissolution of β-HgS_(s). A secondary Fe-bearing phase resembling poorly formed green rust was observed in sulfidized solids with scanning electron microscopy, although there was no clear evidence that either surface-bound or mineralized Fe(II) strongly affected Hg speciation. Examination of interrelated processes involving S(-II) and Fe(III) revealed new modes of Hg solubilization previously not considered in Hg reactivity models.  相似文献   

安徽铜陵凤凰山夕卡岩型铜矿床中辉钼矿Re-Os同位素年龄及其地质意义   总被引：5，自引：2，他引：3  

瞿泓滢  裴荣富  王永磊  李进文 《岩石学报》2010,26(3):785-796

铜陵矿集区是我国长江中下游Cu-Au-Fe-Mo成矿带中最重要的有色金属基地之一,凤凰山矿床是铜陵矿集区的重要组成部分,为一个典型的夕卡岩型铜矿床。本文利用Re-Os同位素定年方法对凤凰山铜矿床进行了成矿时代测定,获得了辉钼矿的Re-Os同位素模式年龄范围为139.1±2.4～142.0±2.2Ma,等时线年龄为141.1±1.4Ma,与矿区内石英二长闪长岩和花岗闪长岩SHRIMP锆石U-Pb年龄(144.2±2.3Ma)相吻合,也与铜陵地区其他矿田的成矿时代基本一致,可能为岩石圈减薄事件的成矿响应。  相似文献   

赣南营前岩体的年代学、地球化学、Sr-Nd-Hf同位素组成及其地质意义   总被引：6，自引：1，他引：5  

郭春丽  毛景文  陈毓川 《岩石学报》2010,26(3):919-937

赣南营前岩体由早期似斑状花岗闪长岩和晚期细粒黑云母花岗岩组成,在前者中普遍发育暗色基性包体。SHRIMP锆石U-Pb测年显示似斑状花岗闪长岩为172.2±3.1Ma,细粒黑云母花岗岩为168±3Ma,包体为167.6±3.3Ma。所有的岩石均为钙碱性系列,稀土元素显示LREE富集,HREE亏损,Eu负异常并不明显的特征,Nb-Ta负异常显示壳源物质的特征。晚期细粒黑云母花岗岩、早期似斑状花岗闪长岩、暗色包体的(87Sr/86Sr)i和εNd(t)值分别为0.70885～0.70965、0.71058～1.46393、0.70788～0.70923和-6.38～-5.31、-6.51～-5.17、-5.47～-4.31;锆石εHf(t)值分别为-12.4～-5.7、-9.2～-4.2、-9.4～+0.1。结合岩相学、地球化学研究,初步认为营前岩体的两期花岗质岩石源于地壳重熔,地幔底侵导致地壳熔融形成营前岩体,基性岩浆加入到未冷却的酸性岩浆中形成了目前所见到的暗色包体。结合区域上的研究资料,认为中侏罗世期间,沿"十杭"断裂带及与其相平行的一些深断裂发生了板块的撕裂,这些缝合带是岩石圈相对薄弱的地带,有利于幔源物质底侵上升以及壳幔相互作用。  相似文献   

新疆阿尔泰克因布拉克铜锌矿床地质特征及成矿作用   总被引：4，自引：1，他引：3  

杨富全  毛景文  刘锋  董永观  柴凤梅  耿新霞 《岩石学报》2010,26(2):361-376

克因布拉克中型铜锌矿床赋存于早二叠世花岗岩外接触带的上志留统-下泥盆统康布铁堡组黑云石英片岩、变质石英砂岩中。矿床的形成经历了夕卡岩期、热液期和表生期,铜锌矿主要形成于热液期。矿石中石英和方解石流体包裹体划分为H_2O-NaCl型和H_2O-CO_2(±CH_4/N_2)-NaCl型。成矿温度变化于146～448℃,在170℃、270℃和350℃出现峰值;流体盐度变化于0.2%～46.9%NaCl_(eq),峰值为1.5%NaCl_(eq)和5.5%NaCl_(eq);流体的密度0.55～1.19g/cm~3。硫化物的δ~(34)S集中变化于-8.4‰～1.9‰,峰值为0‰,表明硫来自岩浆。石英和方解石δD_(SMOW)介于-130‰～-79‰,δ~(18)O_(SMOW)值介于8.0‰～11.6‰,δ~(18)O_(H2O)值为-1.7‰～4.43‰,表明成矿流体主要是岩浆水,混合大气降水。方解石中δ~(13)C_(PDB)变化于-5.3‰～-1.1‰,暗示碳来自花岗质岩浆。成矿时代为早中二叠世,成矿作用与花岗质岩浆期后的热液活动有关。  相似文献   

Systematic winds at heights between 350 and 675 km from analysis of the orbits of four balloon satellites     

Jack W. Slowey 《Planetary and Space Science》1975,23(5):879-886

Six values of the rate of rotation of the Earth's upper atmosphere have been obtained by analysis of the orbital inclinations of four balloon satellites in the intervals just before the final decay of their orbits. The effective heights of these results range from about 350 to about 675 km. The values themselves range from 0·8 to 1·4 times the Earth's rotation and correspond to zonal wind speeds between 100 m/sec westward and 200 m/sec eastward. All the results correspond to fairly specific local times and are consistent with a diurnal wind pattern in low latitudes having a strong eastward maximum near local midnight and a lesser westward maximum near 10:00 LT. They argue against the contention of a sharp decrease in the rate with respect to that of the Earth, which is supposed to begin at about 360 km. The factors involved in the determination of these values and the method used are discussed in considerable detail.  相似文献   

豫西沙沟脉状Ag-Pb-Zn矿床地质特征和成矿流体研究   总被引：6，自引：1，他引：5  

高建京  毛景文  叶会寿  陈懋弘  郑榕芬 《岩石学报》2010,26(3):740-756

豫西沙沟薄脉状Ag-Pb-Zn硫化物矿床位于华北陆块南缘熊耳山地区,主要由多金属硫化物-石英-碳酸盐脉型和石英-碳酸盐-绢云母-多金属硫化物蚀变岩型两种矿化类型组成。主要矿脉的矿物共生序列可以分为成矿前的石英-黄铁矿阶段(Ⅰ)、闪锌矿-石英-方铅矿-少量银矿物阶段(Ⅱ1)、方铅矿-石英-闪锌矿-含铁白云石-银矿物阶段(Ⅱ2)和成矿后的方解石-(石英)阶段(Ⅲ)。对不同阶段的成矿流体研究表明,石英-黄铁矿阶段(Ⅰ)中的含氯化钠子晶三相(LVH)包裹体(Ⅰ1)可能是直接从饱和水的结晶岩浆熔体中出溶形成或是由岩浆流体的减压沸腾形成,显示该区很可能存在岩浆流体端元。多金属硫化物阶段(Ⅱ1Ⅱ2)捕获富液相包裹体(LV型)和个别CO2包裹体(C型),这两个阶段流体包裹体反映了主成矿阶段流体的基本特征,结合包裹体气相和液相成分色谱分析以及包裹体初融温度,认为成矿流体应该为中-低温低盐度含CO2的H2O-NaCl体系。其中,阶段(Ⅱ2)的均一温度(145～288℃,平均为194℃)比阶段(Ⅱ1)的均一温度(185～357℃,平均240℃)低46℃;同时,阶段(Ⅱ2)的盐度(1.91%～10.86%,平均6.38%)较阶段(Ⅱ1)盐度(4.65%～10.11%,平均7.77%)略低。对这一温度和盐度的总体下降趋势的合理解释是大气水的逐渐混入。多金属硫化物阶段(Ⅱ1Ⅱ2)之后的方解石-(石英)阶段普遍为富液相包裹体(LV型),该阶段显著降低的温度(129～208℃,平均165℃)和盐度(1.40%～4.03%,平均2.50%),进一步佐证大气水的不断混入。而且,流体混合可能在引起矿石矿物从热液中沉淀方面起到重要作用。  相似文献   

湖北铜绿山矿床石英闪长岩的矿物学及Sr-Nd-Pb同位素特征   总被引：11，自引：8，他引：3  

赵海杰  毛景文  向君峰  周振华  魏克涛  柯于富 《岩石学报》2010,26(3):768-784

铜绿山是长江中下游鄂东南矿集区最重要的、大型夕卡岩型Cu-Fe(Au)矿床。本文对该矿区中与成矿密切的石英闪长岩进行了详细的矿物成分、地球化学及Sr-Nd-Pb同位素研究。结果表明:岩石中斜长石主要为更长石(An=21～31);角闪石贫Ti(0.2),高Mg/(Mg+Fe)(0.5),属于富镁角闪石;而黑云母为镁质黑云母。岩石的地球化学具有高硅(58.86%～67.71%),富碱(Na2O+K2O=5.67%～9.63%),富集轻稀土元素(LREE)和大离子亲石元素(LILE),并强亏损元素Nb、Ta、Ti等特征。岩石的(87Sr/86Sr)i为0.7055～0.7069,εNd(t)为-7.65～-3.44;(206Pb/204Pb)i=17.66～18.00,(207Pb/204Pb)i=15.49～15.56,(208Pb/204Pb)i=37.73～38.19。矿物成分、地球化学和同位素特征说明,铜绿山岩体与阳新岩体为同源岩浆的产物,源区为深度大于40km的富集地幔,经下地壳的混染及分离结晶作用形成。岩浆熔体形成的温度应大于889℃。角闪石和黑云母的温度计估算岩浆结晶温度分别为650～800℃和500～630℃,黑云母开始结晶温度略低于角闪石结晶结束温度,压力为1.49kbar,对应侵位深度约4.9km。岩浆具有利于Cu、Fe、Au等成矿元素进入熔体的条件,可能与板块俯冲作用相关。  相似文献   

Benthic foraminiferal Mg/Ca-paleothermometry: a revised core-top calibration     

Caroline H Lear  Yair RosenthalNiall Slowey 《Geochimica et cosmochimica acta》2002,66(19):3375-3387

Core-top samples from different ocean basins have been analyzed to refine our current understanding of the sensitivity of benthic foraminiferal calcite magnesium/calcium (Mg/Ca) to bottom water temperatures (BWT). Benthic foraminifera collected from Hawaii, Little Bahama Bank, Sea of Okhotsk, Gulf of California, NE Atlantic, Ceara Rise, Sierra Leone Rise, the Ontong Java Plateau, and the Southern Ocean covering a temperature range of 0.8 to 18°C were used to revise the Cibicidoides Mg/Ca-temperature calibration. The Mg/Ca-BWT relationship of three common Cibicidoides species is described by an exponential equation: Mg/Ca = 0.867 ± 0.049 exp (0.109 ± 0.007 × BWT) (stated errors are 95% CI). The temperature sensitivity is very similar to a previously published calibration. However, the revised calibration has a significantly different preexponential constant, resulting in different predicted absolute temperatures. We attribute this difference in the preexponential constant to an analytical issue of accuracy. Some genera, notably Uvigerina, show apparently lower temperature sensitivity than others, suggesting that the use of constant offsets to account for vital effects in Mg/Ca may not be appropriate. Downcore Mg/Ca reproducibility, as determined on replicate foraminiferal samples, is typically better than 0.1 mmol mol⁻¹ (2 S.E.). Thus, considering the errors associated with the Cibicidoides calibration and the downcore reproducibility, BWT may be estimated to within ±1°C. Application of the revised core-top Mg/Ca-BWT data to Cenozoic foraminiferal Mg/Ca suggests that seawater Mg/Ca was not more than 35% lower than today in the ice-free ocean at 50 Ma.  相似文献   

How to overcome inter-electrode variability and instability to quantify dissolved oxygen, Fe(II), mn(II), and S(?II) in undisturbed soils and sediments using voltammetry     

Slowey AJ  Marvin-Dipasquale M 《Geochemical transactions》2012,13(1):6-20

Background

Although uniquely capable of measuring multiple redox constituents nearly simultaneously with no or minimal sample pretreatment, voltammetry is currently underutilized in characterizing redox conditions in aquatic and terrestrial systems. Investigation of undisturbed media such as pore water requires a solid-state electrode, and such electrodes can be difficult to fabricate reproducibly. An approach to determine the concentrations of electroactive constituents using indirectly calibrated electrodes has been developed, but the protocol for and accuracy of this approach??the pilot ion method??has not been documented in detail.

Results

A detailed procedure for testing electrode quality is provided, and the application and limitations of the pilot ion method have been documented. To quantify Fe(II) and Mn(II), subtraction of non-linear baseline functions from voltammetric signals produced better calibration curves than did linear baselines, enabled lower detection limits and reliable deconvolution of overlapping signals, and was successfully applied to sediment pore water signals. We observed that electrode sensitivities often vary by tens of percent, and that the sensitivity declines over time. The ratio of calibration slopes of Mn(II) to Fe(II) varied by no more than 11% from one Hg/Au electrode to another and Fe(II) concentrations predicted by the Mn(II) pilot ion were, on average, 13% different from their actual values. However, concentration predictions by the pilot ion method were worse for less than 15???M Fe(II) (46% different on average). The ratio of calibration slopes of Mn(II) to S(?II) varied by almost 20% from one Hg/Au electrode to another, and S(?II) predicted concentrations were as much as 58% different from their actual values. These predictions of Fe(II) and S(?II) concentrations indicate that the accuracy of the pilot ion method depends on how independent calibration slope ratios are from the electrode used. At medium-to-high concentration for the ocean, naturally derived dissolved organic carbon did not significantly affect the baseline-corrected electrode response of Mn(II) and Fe(II), but did significantly affect the response of S(?II).

Conclusions

Despite their intrinsic variability, Hg/Au electrodes fabricated by hand can be used to quantify O₂, S(?II), Fe(II), and Mn(II) without calibrating every electrode for every constituent of interest. The pilot ion method can achieve accuracies to within 20% or less, provided that the underlying principle??the independence of slope ratios??is demonstrated for all voltammetric techniques used, and effects of the physicochemical properties of the system on voltammetric signals are addressed through baseline subtraction.  相似文献