Microbial response to surface microtopography: the role of metabolism in localized mineral dissolution

We examine the role of microtopographical surface features on sulfide minerals in localizing and aligning bacterial adhesion. Experimental data shows strong correlation between bacterial cell alignment and principal crystallographic axes of pyrite (100 and 110). While bacteria often adhere to visible surface imperfections such as scratches, in many cases no associated surface features are visible. Additionally, the size of the surface imperfection does not unambiguously determine its effect in localizing and aligning bacterial cells. We theoretically model bacterial adhesion. We find that the depth of a surface feature such as a scratch is less important than its cross-sectional shape. Surface features that conform to the bacterial shape can strongly alter local bacterial adhesion energies, even with heights of only 10 nm. Hence, small local surface alterations due to bacterial metabolism could strongly affect local adhesion parameters, and may account for the observed bacterial distributions on mineral surfaces.     

扬子地台灯影组碳酸盐岩中的硫和碳同位素记录

扬子地区灯影组的海相碳酸盐岩地层不仅记录了当时海水的碳同位素变化，也保存了海水的硫同位素记录，能够通过测定所提取的微量硫酸盐的硫同位素组成来获得。灯影组碳酸盐岩中微量硫酸盐的δ^34S值大部分在 20.0‰～ 38．7‰之间变化，碳酸盐岩的δ^13C值变化在 0．5‰～ 5．0‰之间。除灯影组顶、底界线处外，δ^34S和δ^13C值总体上变化幅度较小，大体上呈逐渐降低的变化趋势。灯影组碳酸盐岩中连续的硫、碳同位素记录分别反映了同期海水中溶解硫酸盐和碳酸盐的硫、碳同位素的变化特征。灯影组微量硫酸盐和碳酸盐岩的同位素特征，意味着灯影期海洋中具有高的生物产率和有机碳埋藏速率；除了顶底界线处，具有相对稳定的古气候条件和古海洋环境。灯影期海水的δ^34S值和δ^13C值同时呈逐渐降低的变化趋势，可能是由海洋深部水体逐渐氧化所致。     

Geochemical constraints on the genesis of the Pb–Zn deposit of Jalta (northern Tunisia): Implications for timing of mineralization,sources of metals and relationship to the Neogene volcanism

The occurrence of Pb–Zn deposits of Jalta district (northern Tunisia) as open space fillings and cements and breccia in the contact zones between Triassic dolostones and Miocene conglomerates along or near major faults provides evidence of the relationship between the mineralization and tectonic processes. Pb isotopes in galena from the deposits yielded average ²⁰⁶Pb/²⁰⁴Pb, ²⁰⁷Pb/²⁰⁴Pb and ²⁰⁸Pb/²⁰⁴Pb ratios of 18.821, 15.676 and 38.837, respectively, implying a well-mixed multi-source upper crustal reservoir of metals. Magmatism and compressional tectonism during the Alpine orogeny favored Pb–Zn mineralization in the Jalta district. The enrichment in Pb, Zn, Cd and Co of the Triassic carbonates and enrichments in Pb, Zn and Cd in Triassic clayey shales is associated with hydrothermal alteration around faults. Alunite in the deposit has δ³⁴S values (−2.5 to −1.5‰ VCDT), which could have been formed at and above the water table in a kind of steam-heated environment, where fluids containing H₂S mixed with fluids containing K and Al. The H₂S could have been produced by TSR of sulfates at high temperature at depth and then leaked upward through deep-seated faults, whereas the K and Al could have been acid-leached from Miocene volcanic rocks.     

两广地区自然硫释放量的研究

全球和区域大气环境研究的重要任务之一是查明各种气态物质自然源释放通量,含硫化合物是其中的一种,它在阐明生物圈硫循环和环境酸化中起重要作用.迄今为止,我国尚无有关研究报道.本文参考文献资料和实测数据用类比法进行了我国两广地区自然源硫化物释放量的计算.结果表明,天然源硫化物中主要是来自树木和土壤,释放的硫化物为COS(49％),DMS(32％)和H_2S(14％).两广地区全年自然源硫释放量3325吨(以硫计).     

Study of metal aerosol systems as a sink for atmospheric SO2

The chemical removal of SO₂ in the presence of different aerosol systems has been investigated in laboratory experiments using a dynamic flow reactor. The aerosols consisted of wetted particles containing one of the following substances: MnCl₂, Mn(NO₃)₂, MnSO₄, CuCl₂, Cu(NO₃)₂, CuSO₄, FeCl₃, NaCl. The SO₂ removal rate R was measured as a function of the SO₂ gas phase concentration (SO₂)_g, the spatial metal concentration C_Me, and the relative humidity rH in the reactor. A first-order dependence with regard to (SO₂)_g was observed for each type of aerosol. For the Mn(II) and Cu(II) aerosols R was found to be a non-linear function of C_Me except for MnSO₄ and Cu(NO₃)₂ particles. The removal rate showed a significant increase with the relative humidity particularly when rH was close to the deliquescence point of the wetted particles. Among the Mn(II) and Cu(II) aerosols investigated Mn(NO₃)₂ was found to be most efficient for the chemical removal of SO₂ at atmospheric background conditions, especially in haze and fog droplets. The results further indicate that the catalytic oxidation of S(IV) in such aerosol systems may be as efficient as its oxidation by H₂O₂ in cloud water.     

Kerogen based characterization of major gas shales: Effects of kerogen fractionation

Research into the origin and the mode of entrapment and expulsion of natural gas from unconventional plays requires the isolation and separation of kerogen in its purest and most intact form from the rock matrix. This study expands on the comparative analysis of the effects that isolation methods, conservative closed system versus conventional open system, have on kerogen’s elemental, isotopic and physical properties. Four major gas shales, including the Barnett, the Marcellus, the Haynesville and a Polish gas shale, were chosen. In addition, the Monterey shale, though not strictly a gas shale, was included to address the effects on sulfur rich, Type II-S kerogen.Results indicate that the kerogen residues from the conventional open system method showed lower recovery and higher mineral content than those from the conservative closed system method. Differences were manifested in the elemental analysis data, where kerogens isolated using the open system method showed a significant deficit in the organic C, H, O, S and N material balance. Furthermore, the recovered residues show different sulfur content and δ³⁴S composition, most likely attributable to differences in pyrite content. Nevertheless, the relative abundances of the various macerals in the kerogen residues from the same parent shale are not very different; neither was the bulk δ¹³C composition of the recovered residues. This is not particularly surprising, considering that in all the five cases examined in this study, the organic matter was fairly homogeneous.     

LA-(MC)-ICPMS和(Nano)SIMS硫化物微量元素和硫同位素原位分析与矿床形成的精细过程

硫化物微区原位分析技术包括LA-ICPMS定点微量元素分析、LA-ICPMS和(Nano) SIMS微量元素面扫描分析,以及SIMS、Nano SIMS和LA-MC-ICPMS原位硫同位素点分析和面扫描。这些分析方法可以有效地获取不同期次硫化物微量元素含量、丰度分布图像、硫同位素比值和分布特征,结合微区时间分辨信号谱图、微量元素相关性分析等,在矿床学的成矿元素行为与赋存状态、成矿元素置换反应、成矿流体与硫的来源、矿石矿物的化学分带性、矿床成因模型等研究中有着重要的应用前景,以探讨矿床的精细成矿过程。硫化物原位微量元素和同位素LA-(MC)-ICPMS和(Nano) SIMS分析,需要降低仪器和分析方法的系统误差,克服严重的基体效应和同位素分馏效应。     

黔南坳陷油苗来源:碳、硫同位素及生物标志物证据

为明确黔南坳陷不同层位油苗来源,在广泛采集不同层位烃源岩、油苗样品的基础上,采用GC、GC-MS及GC-IRMS等方法对其碳、硫同位素及生物标志物特征进行系统分析,进而开展了油源对比.结果表明:油苗的δ13C值为-33.04‰～-31.63‰,平均-32.26‰(n=18);δ34S值为+16.06‰～+23.06‰,平均+18.99‰(n=4);油苗遭受不同程度生物降解,常规甾、萜烷面貌特征差异较大,但普遍含有较丰富的三环萜烷、伽玛蜡烷、三芳甾烷、芳基类异戊二烯烃、惹烯和硫芴;C25三环萜烷/C24四环萜烷值、二苯并噻吩/菲与Pr/Ph相关图表明油苗为典型海相原油;Ts/(Ts +Tm)、C29甾烷20S/(20S+ 20R)及甲基菲指数等均表明油苗为成熟-高熟原油.研究区下寒武统牛蹄塘组黑色泥岩干酪根δ13C值为-35.79‰～-29.88‰,平均-32.85‰(n=35),与油苗相关性良好,而泥盆系、石炭系和二叠系烃源岩δ13C值显著偏重,均大于-29‰;下寒武统牛蹄塘组黑色泥岩干酪根δ34S值为+ 14.78‰～+ 17.60‰,平均+16.32‰(n=4),与油苗具有很好的可比性,而下、中泥盆统黑色泥岩干酪根δ34S值分别为-9.10‰～-6.78‰和+0.63‰～ +7.93‰,二叠系煤系地层有机质δ34S值为-7.40‰～+4.00‰,均显著偏轻.此外,下寒武统黑色泥岩普遍含有较丰富的伽玛蜡烷、三芳甾烷、芳基类异戊二烯烃和惹烯,三芴系列中硫芴含量极高,其它几套黑色泥岩则不合或贫含三芳甾烷和惹烯,伽玛蜡烷和硫芴含量亦较低.综合认为油苗具相同来源,且均与研究区下寒武统黑色泥岩具有较好亲缘关系.     

Sulfur redox reactions: Hydrocarbons,native sulfur,Mississippi Valley-type deposits,and sulfuric acid karst in the Delaware Basin,New Mexico and Texas

Hydrocarbons, native sulfur, Mississippi Valley-type (MVT) deposits, and sulfuric acid karst in the Delaware Basin, southeastern New Mexico, and west Texas, USA, are all genetically related through a series of sulfur redox reactions. The relationship began with hydrocarbons in the basin that reacted with sulfate ions from evaporite rock to produce isotopically light ( ³⁴S = -22 to -12) H₂S and bioepigenetic limestone (castiles). This light H₂S was then oxidized at the redox interface to produce economic native sulfur deposits ( ³⁴S = -15 to +9) in the castiles, paleokarst, and along graben-boundary faults. This isotopically light H₂S also migrated from the basin into its margins to accumulate in structural (anticlinal) and stratigraphic (Yates siltstone) traps, where it formed MVT deposits within the zone of reduction ( ³⁴S = -15 to +7). Later in time, in th zone of oxidation, this H₂S reacted with oxygenated water to produce sulfuric acid, which dissolved the caves (e.g., Carlsbad Cavern and Lechuguilla Cave, Guadalupe Mountains). Massive gypsum blocks on the floors of the caves ( ³⁴S = -25 to +4) were formed as a result of this reaction. The H₂S also produced istopically light cave sulfur ( ³⁴S = -24 to -15), which is now slowly oxidizing to gypsum in the presence of vadose drip water.     

脱氮硫杆菌同步脱硫反硝化技术的关键因素研究

利用脱氮硫杆菌(Thiobacillus denitrificans)在厌氧条件具有的脱硫反硝化生理特性,提出同步脱硫反硝化技术的思路,推导出脱氮硫杆菌(Thiobacillus denitrificans)氧化硫化物为单质硫的化学计量式,并通过间歇试验考察同步脱硫反硝化技术的关键因素。试验结果表明,硫氮比(S~(2-)/NO_3~-比值)和硫化物浓度是同步脱硫反硝化技术的关键因素,两者分别控制在5/3和低于300mg/L的水平可以获得较好的脱硫和反硝化效果,在此条件下,单质硫转化率最高达94％,且随着硫氮比的降低而升高。