Micromechanical modeling for rate‐dependent behavior of salt rock under cyclic loading

The dependence of rock behavior on the deformation rate is still not well understood. In salt rock, the fundamental mechanisms that drive the accumulation of irreversible deformation, the reduction of stiffness, and the development of hysteresis during cyclic loading are usually attributed to intracrystalline plasticity and diffusion. We hypothesize that at low pressure and low temperature, the rate‐dependent behavior of salt rock is governed by water‐assisted diffusion along grain boundaries. Accordingly, a chemo‐mechanical homogenization framework is proposed in which the representative elementary volume (REV) is viewed as a homogeneous polycrystalline matrix that contains sliding grain‐boundary cracks. The slip is related to the mass of salt ions that diffuse along the crack surface. The relationship between fluid inclusion‐scale and REV‐scale stresses and strains is established by using the Mori–Tanaka homogenization scheme. It is noted from the model that a lower strain rate and a larger number of sliding cracks enhance stiffness reduction and hysteresis. Thinner sliding cracks (i.e., thinner brine films) promote stiffness reduction and accelerate stress redistributions. The larger the volume fraction of the crack inclusions, the larger the REV deformation and the larger the hysteresis. Results presented in this study shed light on the mechanical behavior of salt rock that is pertinent to the design of geological storage facilities that undergo cyclic unloading, which could help optimize the energy production cycle with low carbon emissions.     

The initial assessment of trace metal pollution in coastal sediments

Coastal sediments are important hosts for pollutant trace metals, but analytical difficulties can prevent them being included in routine environmental monitoring programmes. In order to identify a suitable approach to the problem, an established simple technique has been evaluated for the initial assessment of trace metal pollution in coastal sediments. The technique, which involves leaching the samples with cold 0.5 N HCl, has been applied to surface sediments from two Greek gulfs and has been shown to provide a rapid, inexpensive way of initially establishing the gross degree to which a sediment population has been subjected to trace metal pollution from the overlying waters.     

The distribution of zinc,nickel, manganese,cadmium, copper,and iron in some surface waters from the world ocean

Determinations of Zn, Ni, Mn, Cd, Cu, and Fe have been carried out on 51 near-shore and 38 open-ocean surface seawaters from various regions of the World Ocean.The concentrations of the trace metals have been established in the open-ocean waters, and have been used as “baselines” to evaluate trace-metal enhancement in near-shore regions. The factors by which the trace metals are enriched in near-shore regions vary from one element to another and, according to the highest concentration factors found, decrease in the order Zn = Mn > Cd = Cu = Ni.These elements exhibit differences in their distributions between near-shore and open-ocean waters, and they have been divided into two types on this basis: Type I, in which the largest number of samples in both shelf and open-ocean waters lie in the same concentration range. Zinc, cadmium, and copper are Type I elements. Type 2, in which the largest number of samples of near-shore waters lie in a higher concentration range than the largest number of samples of open-ocean waters. Nickel and manganese are Type 2 elements.The concentrations of Mn, Cd and Zn are similar in open-ocean surface waters from the South Atlantic and Indian Ocean, but Cu and Ni have higher concentrations in the former ocean.There is considerable variation in the concentrations of the trace metals in near-shore surface waters from various regions of the World Ocean. These variations are discussed in detail.     

The distribution of particulate organic carbon and nitrogen in some surface waters of the World Ocean

Data is presented for the concentrations of organic carbon and nitrogen, and C:N ratios, in marine particulate matter, and for POC and PN, from surface waters collected in the northeastern Atlantic, South Atlantic, Indian Ocean and China Sea.The organic carbon content of this particulate matter varies between 4.6% and 29.9%, and has an average of 17.8%. The average organic carbon content of particulate matter from the various oceans decreases in the order: Northeastern Atlantic > South Atlantic > Indian Ocean > China Sea.The nitrogen content of the particulate matter varies between 1.0% and 3.9%, with an average of 2.2%, and in general follows the same trend as that of organic carbon.C:N ratios vary between 5.1 and 10.6, and have an average of 7.9.The POC contents of the oceanic waters vary between 6.6 and 211 μg/l, with an average of 52 μg/l. The concentrations in the surface waters decrease in the following order: Northeastern Atlantic τ China Sea > South Atlantic > Indian Ocean.The concentrations, and compositions, of particulate matter from various coastal localities are given for comparison with the oceanic values.     

新疆阿尔泰铁木尔特铅锌矿床流体包裹体研究及地质意义

铁木尔特中型铅锌矿是阿尔泰山南缘克兰盆地内的重要VMS型矿床。矿床赋存于上志留统-下泥盆统康布铁堡组上亚组第二岩性段,容矿岩石为大理岩、绿泥石英片岩、变钙质粉砂岩、夕卡岩。矿体呈似层状和透镜状。矿床的形成经历了喷流沉积期、叠加改造期和表生期。石英、长石、方解石和石榴子石中包裹体类型主要为液体包裹体,在石英中另出现了气体包裹体、纯气体包裹体、含子矿物多相包裹体、含液体CO2的三相包裹体和两相CO2包裹体。喷流沉积期成矿流体均一温度变化于150～330℃,其峰值是165℃和285℃,成矿流体盐度(NaCleq)为4%～16%,流体密度为0.77～0.97g/cm3,流体阳离子主要以Na+为主,次之为K+,阴离子以Cl-为主,其次是SO42-,气相成分主要是H2O和CO2。叠加改造期均一温度范围是150～480℃,峰值为285℃,盐度(NaCleq)为2.2%～17.08%和33.93%～47.2%,流体密度变化于0.61～1.03g/cm3之间,流体阳离子主要以Na+为主,次为K+、Mg2+、Ca2+,阴离子以Cl-为主,其次是SO42-,气相成分主要是H2O和CO2,其次为N2、CH4,含有少量C2H6。     

新疆包古图斑岩铜矿床成矿流体及成矿物质来源——来自硫、氢和氧同位素证据

包古图大型斑岩铜矿位于准噶尔盆地西缘。铜矿化主要呈浸染状、细脉浸染状分布于似斑状(石英)闪长岩、闪长玢岩、隐爆角砾岩和少量花岗闪长岩中。依据矿脉的穿插关系和矿物组合,成矿过程经历了黑云母-钾长石-钠长石阶段、石英-硫化物阶段和石英碳酸盐阶段。矿脉中石英的δDSMOW值介于-107‰～-86‰,δ18OSMOW值变化于11.3‰～16.2‰,δ18OH2O值为4.4‰～9.3‰,表明成矿流体来源为深源的岩浆水。硫化物的δ34S值介于-5.1‰～0.7‰,平均为-1.8‰,表明硫来源于深部岩浆或地幔。结合Ⅱ、Ⅲ和Ⅴ号含矿岩体锆石LA-ICP-MSU-Pb年龄及辉钼矿Re-Os年龄,推断包古图铜矿床成矿作用发生在晚石炭世,与中酸性斑岩体的侵入有密切成因关系。     

Particulate aluminium fluxes in the eastern Atlantic

The atmospheric, primary down-column and sedimentary fluxes of particulate aluminium (Al_p) have been calculated for a number of regions in the Atlantic Ocean.The vertical down-column flux of Al_p from Atlantic surface waters exhibits a strong geographical variation, and its magnitude is influenced by supply mechanisms, which control the surface Al_p concentrations, and primary production, which affects the rate of down-column transport. Overall, the down-column transport of Al_p is greatest in the marginal regions of the Atlantic. In the eastern margins the highest surface water concentrations are found in the region lying between ～30°N and ～10°N, i.e. under the general path of the northeast trades. In this region there is excellent agreement between the dry (i.e. 1 cm^?1 s^?1 deposition velocity) atmospheric flux (～80 000 ng Al_p cm^?2 y^?1), the primary vertical down-column flux ($\text{? 70 000}\text{ng Al}{}_{\mathrm{p}}\text{cm}{}^{\mathrm{?2}}\text{y}{}^{\mathrm{?1}}$) and the sediment flux (～90 000 ng Al_p cm^?2 y^?1). In the regions to the north (i.e. ～40°N to ～30°N) and to the south (i.e. ～10°N to ～5°S) the primary down-column Al_p flux decreases to an average of ～19 000 μg cm^?2 y^?1, which makes a direct maximum contribution of ～20% of the sediment Al_p requirement. In the open-ocean South Atlantic the primary down-column flux of Al_p is ～3300 μg cm^?2 y^?1, this is similar to the dry (i.e. 1 cm^?1 s^?1 deposition velocity) atmospheric flux, and contributes ～20% of the Al_p required by the underlying deep-sea sediment.     

An approach to the assessment of local trace metal pollution in the Mediterranean marine atmosphere

Assessing the extent of local trace metal pollution in marine atmospheric particulates presents a number of difficulties, and one potential approach to the problem has been evaluated by reference to a series of aerosols from the lower troposphere over the Eastern Mediterranean. This region, which is less remote from the continents than open-ocean areas, has two significantly different atmospheric particulate catchments: being bordered in the north by nations having industrialized, semi-industrialized and rural economies, and in the south by the North African desert belt. The elemental chemistry of the particulates is illustrated in terms of the distributions of Fe and Pb, which are presented in the form of enrichment factor diagrams, and is shown to be essentially controlled by the dilution of a ‘European’ background material, common to ‘remote’ regions of the latitudinal belt, with crust-derived, desert components. Major local perturbations in the dilution relationship can occur when either crust-derived or pollutant components strongly dominate the total particulate population. The extent of these local perturbations can be tentatively assessed using appropriate enrichment factor diagrams, which offer a framework within which to interpret the elemental chemistry of marine atmospheric particulates providing sufficient data is available for their construction. By using such an EF diagram it is suggested that the Eastern Mediterranean atmospheric particulates have not suffered local pollution on a gross scale with respect to Pb.     

Mercury in some surface waters of the world ocean

Mercury concentrations in mid-latitude eastern Atlantic surface waters is about twice as high as the oceanic average, perhaps due to pollution. Low concentrations in the tropical Atlantic may be due to uptake by plankton off the west coast of Africa.