黄、东海海域水团发育对底质沉积物分布的影响

通过对黄、东海海域底质沉积物中的细粒级粘土矿物组合特征和全粒级碳酸盐含量分析、对比上覆水团和悬浮体资料，探讨研究区水团发育消长对底质沉积物分布的影响作用。结果表明研究区可以划分为长江冲淡水影响的长江型物质沉积区；黄海水影响的黄河型物质沉积区和黑潮水以及东海次表层水影响的残留型物质沉积区。而水团发育消长可直接影响下伏底质的分布特征。黄河型物质沉积区与残留型物质沉积区的分界相应于黄海冷水向东南扩展与黑潮次中层混合水向陆架爬升互为消长的长期综合平衡位置，而黄海冷水向东南的扩展范围代表着黄河物质在陆架向东南扩展沉积的最大范围．     

罗源湾水母类的生态研究

样品于1986年11月至1987年10月在福建省罗源湾10个站位采集。经鉴定有52种水母。它们可分为沿岸暖水、沿岸暖温和大洋广布三种生态类群。水母类总数量和种类数的季节分布呈单周期,两者高峰均出现在7月。低谷分别出现于11月和1月。在平面分布上,以拟细浅室水母Lensia subtiloides占优势的月份,数量从湾口向湾顶递减,而以球型侧腕水母Pleurobrachia globosa占优势的月份,数量却递增。文中还讨论了水母类的分布和环境因素的关系。     

Internal wave eigenmodes and their weak nonlinear resonant interaction in a nonlinearly stratified fluid—A preliminary theoretical and experimental study

A preliminary theoretical and experimental study was conducted on internal wave modes and their weak nonlinear resonant interaction in a nonlinearly stratified fluid. An asymptotical solution of the modes and a dispersion relation of internal waves in a stratified fluid with density profile similar to that in our experiment were obtained theoretically. The resonant-interaction mechanism to 2nd order approximation is also discussed. The resonant interaction of the 3rd and 4th mode internal waves excited by the unstable 1st mode wave is analyzed on the basis of data obtained by conductivity probes. The resonant-interaction condition, i.e., ,k ₁+k ₃+k ₄=0, is examined. It is shown that the resonant instability increases with pycnocline thickness and wave maker driving frequency. This work is supported by the National Natural Science Foundation of China.     

山东三山岛金矿床流体包裹体特征及其地质意义

三山岛金矿床位于莱州市三山岛—仓上断裂带内,矿石主要为蚀变岩和含金石英脉2种类型。随着胶东金矿床研究的深入和三山岛金矿资源的不断减少,对三山岛金矿床的成矿作用及深部开发前景问题研究具有更重要的意义。针对上述问题,对三山岛金矿床2种类型矿石的成矿流体特征进行对比研究,认为代表成矿早—中期的蚀变岩型矿石形成于中温(均一温度为325～240℃)、低盐度(2.07%～6.88%)、低密度(0.720～0.868g/cm3)、酸碱性不均匀(pH=3.27～10.43)、以氟化物和氯化物为成矿物质载体的还原性流体;代表成矿中—晚期的含金石英脉型矿石形成于中—低温(均一温度为306～160℃)、低盐度(1.05%～9.73%)、低密度(0.739～0.962g/cm3)、碱性(pH=9.25～9.85)、以氯化物和硫化物为成矿物质载体的还原性流体。成矿流体性质的转变反映了成矿流体处于由比较封闭到比较开放的构造环境的转变期,且成矿流体早期以原生岩浆水为主,后期有变质水、大气降水以及海水的参与作用。三山岛金矿成矿深度为2.5～5km,根据目前的开采深度推算其深部还有一定的资源量可供开发。     

胶东半岛大磨曲家金矿床成矿流体物理化学条件演化

胶东大磨曲家金矿床流体包裹体包括水溶液包裹体、富CO2包裹体和高盐卤水包裹体3种类型,前两者发育较多,高盐卤水包裹体发育极少。流体包裹体显微测温及盐度、密度、压力估算显示,水溶液包裹体均一温度为98~376℃,据冰点温度估算,盐度为0.53%~8.28%,水溶液包裹体均一压力低于50×105Pa;富CO2包裹体完全均一温度为255~348℃,盐度为2.42%~11.43%,均一压力为1 000×105~2 500×105Pa;富CO2包裹体中CO2均一温度为23.0~32.4℃,指示该类包裹体可能含有数量不等的CH4或H2S。静水压力体制下,根据纯CO2包裹体均一压力估算成矿深度约为1 km。在270℃左右,均一压力从富CO2包裹体到水溶液包裹体急剧降低,指示成矿流体在270℃左右可能发生过一次减压沸腾过程,成矿流体盐度和密度在270℃左右也有显著的变化。因此,沸腾作用及其引起的成矿流体物理化学条件的急剧变化可能是导致大磨曲家金矿床成矿物质沉淀的重要机制。     

塔东地区古城4井上寒武统—中、上奥陶统流体地球化学示踪

通过对塔东地区古城4井上寒武统和中、上奥陶统碳酸盐岩围岩及充填物的碳、氧、锶同位素地球化学和流体包裹体成分的对比研究表明,充填于中、上奥陶统和上寒武统的流体分属于2个不同来源的流体体系。充填于中、上奥陶统灰岩裂缝中方解石脉的w(87Sr)/w(86Sr)介于0.7084~0.7088,它与早奥陶世海水的w(87Sr)/w(86Sr)相近;流体体系为CH4-H2O体系;充填物与围岩间具有明显的碳、氧同位素差异,表明上部流体体系中的流体来自于奥陶系地层本身。上寒武统白云岩裂缝中方解石脉的w(87Sr)/w(86Sr)为0.7138,明显地高于同时代海水的锶同位素值;流体体系为CO2-H2O体系;下部流体体系中的流体为外来富锶流体。上、下流体体系间互不连通暗示着上寒武统地层具有相对较好的保存条件。     

Carbon and oxygen isotopic composition of car- bonate cements of different phases in terrigenous siliciclastic reservoirs and significance for their origin： A case study from sandstones of the Triassic Yanchang Formation, southwestern Ordos Basin, China

Early carbonate cements in the Yanchang Formation sandstones are composed mainly of calcite with relatively heavier carbon isotope （their δ^18O values range from -0.3‰- -0.1‰） and lighter oxygen isotope （their δ^18O values range from -22.1‰- -19.5‰）. Generally, they are closely related to the direct precipitation of oversaturated calcium carbonate from alkaline lake water. This kind of cementation plays an important role in enhancing the anti-compaction ability of sandstones, preserving intragranular volume and providing the mass basis for later disso- lution caused by acidic fluid flow to produce secondary porosity. Ferriferous calcites are characterized by relatively light carbon isotope with δ^13C values ranging from -8.02‰ to -3.23‰, and lighter oxygen isotope with δ^18O values ranging from -22.9‰ to -19.7‰, which is obviously related to the decarboxylation of organic matter during the late period of early diagenesis to the early period of late diagenesis. As the mid-late diagenetic products, ferriferous cal- cites in the study area are considered as the characteristic authigenic minerals for indicating large-scaled hydrocarbon influx and migration within the clastic reservoir. The late ankerite is relatively heavy in carbon isotope with δ^13C values ranging from -1.92‰ to -0.84‰, and shows a wide range of variations in oxygen isotopic composition, with δ^18O values ranging from -20.5‰ to -12.6‰. They are believed to have nothing to do with decarboxylation, but the previously formed marine carbonate rock fragments may serve as the chief carbon source for their precipitation, and the alkaline diagenetic environment at the mid-late stage would promote this process.     

岩石中的渗透率、流体流动及热液成矿作用

热液成因的固体金属矿床形成过程中都曾拥有一段流动的历史。成矿物质以溶液的形式从矿源地穿过孔隙或断裂达到了现在的栖身之所,在此过程中流体通过的路径决定了它们的走向,而溶液本身也改变了路径的特征。因此,对于此类矿床的研究不能仅仅囿于眼之所见,而应将古流体流动的观念融入其中,并考察它们的跋涉之路。文中总结了近年来国内外在岩石孔隙、断裂介质及与其相关渗透率对热液成矿作用的控制等领域的研究成果和最新进展,对岩石渗透率、渗透率的影响因素、岩石中流体流动的特征等问题进行了阐述,讨论了渗透率对于热液成矿作用深度、成矿规模、矿质沉淀机制等方面的重要影响,藉此在固体金属矿床研究中强化流"体运动"的观念,并促进构造地质学和成矿作用地球化学间一个新研究方向的发展。     

Fluid–Sediment Interaction in a Marine Shallow-Water Hydrothermal System in the Wakamiko Submarine Crater, South Kyushu, Japan

The Wakamiko submarine crater is a small depression located in Kagoshima Bay, southwest Japan. Marine shallow‐water hydrothermal activity associated with fumarolic gas emissions at the crater sea floor (water depth 200 m) is considered to be related with magmatic activity of the Aira Caldera. During the NT05‐13 dive expedition conducted in August 2005 using remotely operated vehicle Hyper‐Dolphine (Japan Agency for Marine‐Earth Science and Technology), an active shimmering site was discovered (tentatively named the North site) at approximately 1 km from the previously known site (tentatively named the South site). Surface sediment (up to 30 cm) was cored from six localities including these active sites, and the alteration minerals and pore fluid chemistry were studied. The pore fluids of these sites showed a drastic change in chemical profile from that of seawater, even at 30 cm below the surface, which is attributed to mixing of the ascending hydrothermal component and seawater. The hydrothermal component of the North site is estimated to be derived from a hydrothermal aquifer at 230°C based on the hydrothermal end‐member composition. Occurrence of illite/smectite interstratified minerals in the North site sediment is attributed to in situ fluid–sediment interaction at a temperature around 150°C, which is in accordance with the pore fluid chemistry. In contrast, montmorillonite was identified as the dominant alteration mineral in the South site sediment. Together with the significant low potassium concentration of the hydrothermal end‐member, the abundant occurrence of low‐temperature alteration mineral suggests that the hydrothermal aquifer in the South site is not as high as 200°C. Moreover, the montmorillonite is likely to be unstable with the present pore fluid chemistry at the measured temperature (117°C). This disagreement implies unstable hydrothermal activity at the South site, in contrast to the equilibrium between the pore fluid and alteration minerals in the North site sediment. This difference may reflect the thermal and/or hydrological structure of the Wakamiko Crater hydrothermal system.     

Geochemical Eccentricity of Ground Water Allied to Weathering of Basalts from the Deccan Volcanic Province,India: Insinuation on CO<Subscript>2</Subscript> Consumption

Analyses of 72 samples from Upper Panjhara basin in the northern part of Deccan Plateau, India, indicate that geochemical incongruity of groundwater is largely a function of mineral composition of the basaltic lithology. Higher proportion of alkaline earth elements to total cations and HCO₃>Cl + SO₄ reflect weathering of primary silicates as chief source of ions. Inputs of Cl, SO₄, and NO₃ are related to rainfall and localized anthropogenic factors. Groundwater from recharge area representing Ca + Mg–HCO₃ type progressively evolves to Ca + Na–HCO₃ and Na–Ca–HCO₃ class along flow direction replicates the role of cation exchange and precipitation processes. While the post-monsoon chemistry is controlled by silicate mineral dissolution + cation exchange reactions, pre-monsoon variability is attributable chiefly to precipitation reactions + anthropogenic factors. Positive correlations between Mg vs HCO₃ and Ca + Mg vs HCO₃ supports selective dissolution of olivine and pyroxene as dominant process in post-monsoon followed by dissolution of plagioclase feldspar and secondary carbonates. The pre-monsoon data however, points toward the dissolution of plagioclase and precipitation of CaCO₃ supported by improved correlation coefficients between Na + Ca vs HCO₃ and negative correlation of Ca vs HCO₃, respectively. It is proposed that the eccentricity in the composition of groundwater from the Panjhara basin is a function of selective dissolution of olivine > pyroxene followed by plagioclase feldspar. The data suggest siallitization (L < R and R _k) as dominant mechanism of chemical weathering of basalts, stimulating monosiallitic (kaolinite) and bisiallitic (montmorillonite) products. The chemical denudation rates for Panjhara basin worked out separately for the ground and surface water component range from 6.98 to 36.65 tons/km²/yr, respectively. The values of the CO₂ consumption rates range between 0.18 × 10⁶ mol//km²/yr (groundwater) and 0.9 × 10⁶ mol/km²/yr (surface water), which indicates that the groundwater forms a considerable fraction of CO₂ consumption, an inference, that is, not taken into contemplation in most of the studies.