The Tambora eruption in 1815 provides a test on possible global climatic and chemical perturbations in the past

A coupled one-dimensional radiative-convective-photochemical diffusion model, which takes into account the influence of ocean inertia on global radiative perturbations is used to investigate the possible climatic and other atmospheric effects of a major volcanic eruption, thought to be similar in magnitude to that of the Tambora eruption, Indonesia, which took place in 1815. A volcanic cloud was introduced in the model stratosphere between 20–25 km and the global average peak aerosol optical thickness was assumed to be 0.25. Both the aerosol optical thickness and aerosol composition, which determine the optical properties, were allowed to vary in the model atmosphere during the life cycle of the volcanic cloud. The results indicate that the global average surface temperature decreases steadily from the date of eruption (7–12 April 1815) with maximum cooling of 1° K occurring in the spring of 1816. The calculations also show significant warming of the stratosphere, with temperature increasing up to 15° K at 25 km in less than six months after the date of eruption. The important effects of the Tambora eruption on stratospheric ozone and UV-B radiation at the surface are also mentioned.     

Resources of the ionized atmosphere as an aerosol source

The potential resources on the ion-stimulated syntheses effects of aerosol particles of lower troposphere in test sites in the arctic, mountain, arid and forest areas as the function of irradiation time and gas-precursor concentration were experimentally and theoretically evaluated. The dust-free outdoor air was irradiated with an ionization current of 10^− 6 A by α-rays from isotope ²³⁹Pu. The total output of radiolytic aerosols (RA) with a diameter of 3–1000 nm was found to be 0.05–0.1 molecules per 1 eV of absorbed radiation, while the physical upper limit is 0.25–0.4 molecules/eV. In an interval of exposition time from 6 to 800 s (adsorbed energy is 3 · 10¹²–10¹⁴ eV/cm³) the RA mass concentration at different sites was increased from 1–10 to 50–500 μg/m³. According to the liquid chromatography data the major RA material is the H₂O/HNO₃ solution with acid concentration  25%. The used physical model presents new aerosols as a product from small and intermediate ion association through formation of neutral clusters and describes adequately some of the peculiarities in field experiment data. Introducing SO₂, NH₃, and also hydrochloric, nitric and sulphuric acid vapours with concentration 0.1–1 mg/m³ in the irradiated air stimulated an increase of mass aerosol concentration by a factor of 8–30. The mean size also decreased by a factor of 3–5. These facts allowed us to expect that the chemical composition of radiolytic aerosols generated in outdoor air would noticeably differ after addition of the gas-precursors.     

不同沉淀法处理含铬废水的比较

含铬废水具有有机物含量高,难降解物质浓度高,色度大,悬浮物多,水质、水量变化大,含有微量毒性物质等特点。本文探讨了在不同参数条件下,硫酸亚铁、铁、硫化亚铁三种还原剂对含铬废水处理效果的影响,实验表明:硫酸亚铁具有明显的优越性,在同等条件下其去除率达到99%以上。     

Aerosol characteristics during winter fog at Agra,North India

Simultaneous measurements on physical, chemical and optical properties of aerosols over a tropical semi-arid location, Agra in north India, were undertaken during December 2004. The average concentration of total suspended particulates (TSP) increased by about 1.4 times during intense foggy/hazy days. Concentrations of SO₄ ²⁻, NO₃ ⁻, NH₄ ⁺ and Black Carbon (BC) aerosols increased by 4, 2, 3.5 and 1.7 times, respectively during that period. Aerosols were acidic during intense foggy/hazy days but the fog water showed alkaline nature, mainly due to the neutralizing capacity of NH₄ aerosols. Trajectory analyses showed that air masses were predominantly from NW direction, which might be responsible for transport of BC from distant and surrounding local sources. Diurnal variation of BC on all days showed a morning and an evening peak that were related to domestic cooking and vehicular emissions, apart from boundary layer changes. OPAC (Optical properties of aerosols and clouds) model was used to compute the optical properties of aerosols. Both OPAC-derived and observed aerosol optical depth (AOD) values showed spectral variation with high loadings in the short wavelengths (<1 μm). AOD value at 0.5 μm wavelength was significantly high during intense foggy/hazy days (1.22) than during clear sky or less foggy/hazy days (0.63). OPAC-derived Single scattering albedo (SSA) was 0.84 during the observational period, indicating significant contribution of absorbing aerosols. However, the BC mass fraction to TSP increased by only 1% during intense foggy/hazy days and thereby did not show any impact on SSA during that period. A large increase was observed in the shortwave (SW) atmospheric (ATM) forcing during intense foggy/hazy days (+75.8 W/m²) than that during clear sky or less foggy/hazy days (+38 W/m²), mainly due to increase in absorbing aerosols. Whereas SW forcing at surface (SUF) increased from −40 W/m² during clear sky or less foggy/hazy days to −76 W/m² during intense foggy/hazy days, mainly due to the scattering aerosols like SO₄ ^2-.     

中国区域气溶胶对东亚夏季风的可能影响(Ⅱ)：黑碳气溶胶及其与硫酸盐气溶胶的综合影响

 利用NCAR的新一代GCM CAM3.0模式耦合一个气溶胶同化系统,研究了中国区域黑碳气溶胶的直接气候效应。结果显示,中国区域黑碳气溶胶引起全球平均辐射强迫为0.13 W/m2,导致除了青藏高原和广西以外的中国大部分地区降温,其中东北、四川和内蒙古中北部降温最显著。由此造成海陆温差缩小,气压差降低,从而总体上使东亚夏季风减弱。但与硫酸盐气溶胶的影响相比,黑碳气溶胶使季风减弱的程度较小,长江中下游地区的降水有所增加。黑碳气溶胶加强了中国东南部地区的对流活动,这与硫酸盐气溶胶的作用相反。同时,探讨了中国区域硫酸盐和黑碳气溶胶的综合直接气候效应。结果表明,硫酸盐和黑碳气溶胶的综合作用与仅有硫酸盐气溶胶的情形十分相似,降水变化的区域也和硫酸盐的保持一致。     

Multiple sulfur isotope chemostratigraphy across the Permian–Triassic boundary at Chaotian,China: Implications for a shoaling model of toxic deep-waters

Previous studies on multiple sulfur isotopes (³²S, ³³S, and ³⁴S) in sedimentary pyrite at the end-Permian suggested a shoaling of anoxic/sulfidic deep-water contributing to the extinction. This scenario is based on an assumption that the sedimentary sulfur cycle was largely controlled by benthos activity, though a stratigraphic correlation between the sulfur records and ichnofabrics of the sediments at the end-Permian has not yet been examined. We report the multiple sulfur isotopic composition of pyrite in the Permian–Triassic boundary interval at Chaotian, South China. Our data can be generally explained by a mixing of sulfur in sulfide from two different sources: one produced via sulfate reduction in an open system with respect to sulfate and the other produced in a closed system. In particular, the former with the substantially low δ³⁴S (<−40 ‰) and high ∆³³S (up to +0.100 ‰) values was likely produced via water-mass sulfate reduction or via sulfate reduction in oxic sediments with common burrows. The frequent occurrence of small pyrite framboids (mostly <5 μm in diameter) in the Lopingian (Late Permian) Dalong Formation of deep-water facies supports the enhanced water-mass sulfate reduction in an anoxic deep-water mass. The negative ∆³³S values are observed only in the oxic limestones, and no substantial ∆³³S change is observed across the extinction horizon despite of the disappearance of bioturbation. Our results are apparently inconsistent with the previous shoaling model. We expand the model and infer that, when the deep-water was sulfidic and its shoaling rate was high, a substantial amount of hydrogen sulfide (H₂S) was supplied onto the shelf via the shoaling; that resulted in the positive ∆³³S value of the bulk sediments. The observed ∆³³S variation on a global scale suggests a substantial variation in H₂S concentration and/or in upwelling rate of shoaling deep-waters during the Permian–Triassic transition.     

云贵高原斜坡地带典型地下水富硫酸盐地区“越层找水”模式及其机理研究

地下水是中国西南云贵高原斜坡地带重要的饮用水源,其中黔中镇宁县北部存在大面积地下水中硫酸盐超标地区,导致了当地出现水质性缺水问题。本次研究通过岩相古地理分析、水化学分析、D、18O、34S同位素测试、岩样测试、岩心观察等技术手段,查明了研究区内地下水的补给源主要为大气降水,地下水中硫酸盐(SO_4~(2-))浓度在30～1100 mg/L,平均值为221.78 mg/L,呈现高度富集SO_4~(2-)的特点;在区域相对隔水层以上,不同类型地下水中SO_4~(2-)浓度大体具有机井上升泉下降泉溶潭地下河出口基岩裂隙泉表层岩溶泉的规律;探讨了地表水、地下水中SO_4~(2-)的来源,表层岩溶泉中硫酸根的来源主要为大气降水,高硫酸盐样品中硫酸根的来源主要为石膏溶解。在此基础上,结合钻井资料,掌握了研究区膏岩层分布及含水层结构特征,通过建立"越层找水"模式,采取下层低硫酸盐含水层,获取合格饮用水源,可有效解决当地水质性缺水问题。     

伊犁蒙其古尔铀矿床含矿层砂岩中黄铁矿形成机制及对铀成矿的指示意义

蒙其古尔铀矿床为伊犁盆地南缘大型层间氧化带砂岩型铀矿床,为查明该矿床含矿层中黄铁矿成因及其形成机制,探讨微生物参与铀成矿过程。文章对含矿层砂岩中黄铁矿与铀矿物矿物学特征、黄铁矿S同位素与碳酸盐胶结物的C-O同位素开展细致研究。研究表明:①蒙其古尔铀矿床中铀主要以铀矿物与吸附铀形式存在,吸附铀主要为有机质吸附铀,铀矿物以沥青铀矿为主,多与黄铁矿、炭屑共生;②蒙其古尔铀矿床含矿层砂岩中黄铁矿主要以自形晶、草莓状和不规则状集合体产出,多与沥青铀矿、碳酸盐胶结物共生,其中黄铁矿S同位素(δ~(34)S_(V-CDT)=-68.4‰～22.1‰)与碳酸盐胶结物的C-O同位素(δ~(13)C_(V-PDB)=-10.2‰～-7.4‰,δ~(18)O_(V-PDB)=-9.6‰～-5.8‰)分析表明黄铁矿具有细菌硫酸盐还原(BSR)与有机物热解2种成因,并探讨了这2种不同成因黄铁矿的形成机制。③结合前人研究成果,认为硫酸盐还原菌(SRB)参与蒙其古尔铀矿床铀成矿过程,以间接还原方式为主,在有机质、黏土矿物与颗粒表面吸附U(Ⅵ)的基础上,通过硫酸盐还原菌(SRB)还原SO_4~(2-)产生的H_2S将U(Ⅵ)被还原成U(Ⅳ),形成铀矿物。     

新型珊瑚海水混凝土力学性能试验研究

为了解决全珊瑚海水混凝土(coral aggregate seawater concrete,简称CASC)的脆性问题,采用碱式硫酸镁水泥(basic magnesium sulfate cement,简称BMSC)为胶凝材料和剑麻纤维为增韧材料制备了一种新型全珊瑚海水混凝土(NCASC),系统测定了基本力学性能,并与普通硅酸盐水泥制备的CASC、碱式硫酸镁水泥砂石混凝土(basic magnesium sulfate cement concrete,简称BMSCC)、普通砂石混凝土(ordinary portland cement concrete,简称OPC)以及普通轻骨料混凝土(lightweight aggregate concrete,简称LAC)的力学性能进行对比。结果表明:立方体抗压强度(f_(cu),m)在15~35 MPa范围内的NCASC的轴心抗压强度(f_c,m)、劈裂抗拉强度(f_(sp),m)与f_(cu),m之间具有较显著的线性关系;对于f_(cu),m为15~35 MPa的混凝土,相同强度NCASC的f_c,m高于OPC、LAC及BMSCC,其f_c,m与f_(cu),m比值最大,大致在0.85~0.96之间,NCASC的f_(sp),m比OPC和LAC高,但比BMSCC低,且随着强度的提高,OPC与NCASC的f_(sp),m间的差距在增大,而LAC和BMSCC与NCASC的f_(sp),m间的差距在缩小;在强度等级C15~C55的范围中,NCASC和CASC的f_(sp),m、f_c,m与f_(cu),m之间的关系基本可以采用相同的线性回归方程来描述,利用这两个回归线性方程得到对应于标准强度等级的CASC和NCASC的f_(sp),m和f_c,m数据,为CASC力学性能研究与结构设计提供参考依据。