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。     

雾水的D和18O同位素研究进展

凝结水的D、¹⁸O同位素研究目前主要集中在雾水方面,露水和土壤吸附水的相关研究仍属空白。由于形成时的温度较高,大多数雾水的D、¹⁸O同位素较当地雨水富集,但不同类型雾的同位素特征存在差异。平流式海洋雾为单级的蒸发—冷凝封闭循环系统的首次凝结,D、¹⁸O同位素较当地雨水显著富集;热带云雾林中的地形雾与降雨同时发生,且水分源于同一云团,δD、δ¹⁸O值差异较小;内陆辐射雾因部分水汽源于当地水分的再循环,过量氘和δD、δ¹⁸O值高于降雨。目前有少量研究用D、¹⁸O同位素指示雾水对植被、地下水和地表径流的补给作用,但以定性分析为主,基于端元混合模型的定量评价极少。露水和土壤吸附水的稳定同位素研究是干旱区凝结水研究的重要方向;D、¹⁸O同位素与其它同位素或化学指标的结合有助于促进凝结水生态水文效应的研究进展;短间隔、高密度的长期观测和用于稳定同位素分析的凝结水采样器的设计是需要进一步开展的工作。     

西湖茶园茶叶铅污染铅同位素示踪

通过对西湖茶园的植物和土壤样品进行一系列的调查,以着力寻找茶叶的铅污染源。利用铅同位素技术对西湖茶园的土壤、茶叶和城区的燃煤、大气气溶胶、汽车尾气进行铅同位素示踪研究。研究表明,茶园土壤铅物质的可溶相具同源性和残查态偏于多源性。清洗后的茶叶铅含量显著降低,但其同位素组成不发生明显改变,显示出茶叶中的铅与叶面空气沉降物中的铅同源。不同介质铅同位素对比值平均值呈现表土、大气(气溶胶)、煤的w(²⁰⁶Pb)/w(²⁰⁷Pb)与茶叶趋于相近,汽油低之;表土、大气(气溶胶)、汽油的w(²⁰⁸Pb)/〔w(²⁰⁶Pb)+w(²⁰⁷Pb)〕与茶叶趋于相近,煤略高之。不同区域茶叶铅物质具同源性,与种植的农业地质背景无关。在煤燃烧、气化过程中,Pb进入大气,通过大气沉降或被茶树吸收或附着在茶叶叶面;汽车尾气的排放是茶树铅污染的重要原因之一。     

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.     

锶掺杂的正铌酸镧超细粉体的合成与性能

采用溶胶低温燃烧法和高温固相反应法制备了锶掺杂的正铌酸镧（La0.95Sr0.05NbO4）超细陶瓷粉体。应用XRD、SEM和激光粒度分析仪等对陶瓷粉体的物相、粒度和粒度分布进行了表征,同时考察了两种方法制备的粉体的烧结性能。结果表明：采用溶胶低温燃烧法制备的La0.95Sr0.05NbO4（LSNb）为粒径〈100 nm、粒度分布范围窄的超细粉体;高温固相反应法制备的粒径为0.5-1.0μm、呈球形的LSNb超细陶瓷粉体。溶胶低温燃烧法制备的粉体在1 250℃烧结10 h形成致密的陶瓷片;高温固相反应法制备的粉体在1 400℃以上烧结10 h致密。两种LSNb致密膜均具有一定的透氢作用,900℃氢渗速率分别为1.96×10^-3mL·cm^-2·min^-1和1.67×10^-3mL·cm^-2·min^-1。     

Determination of Sr/Sr mass-dependent isotopic fractionation and radiogenic isotope variation of Sr/Sr in the Neoproterozoic Doushantuo Formation

We measured both mass-dependent isotope fractionation of δ⁸⁸Sr (⁸⁸Sr/⁸⁶Sr) and radiogenic isotopic variation of Sr (⁸⁷Sr/⁸⁶Sr) for the Neoproterozoic Doushantuo Formation that deposited as a cap carbonate immediately above the Marinoan-related Nantuo Tillite. The δ⁸⁸Sr and ⁸⁷Sr/⁸⁶Sr compositions showed three remarkable characteristics: (1) high radiogenic ⁸⁷Sr/⁸⁶Sr values and gradual decrease in the ⁸⁷Sr/⁸⁶Sr ratios, (2) anomalously low δ⁸⁸Sr values at the lower part cap carbonate, and (3) a clear correlation between ⁸⁷Sr/⁸⁶Sr and δ⁸⁸Sr values. These isotopic signatures can be explained by assuming an extreme greenhouse condition after the Marinoan glaciation. Surface seawater, mixed with a large amount of freshwater from continental crusts with high ⁸⁷Sr/⁸⁶Sr and lighter δ⁸⁸Sr ratios, was formed during the extreme global warming after the glacial event. High atmospheric CO₂ content caused sudden precipitation of cap carbonate from the surface seawater with high ⁸⁷Sr/⁸⁶Sr and lighter δ⁸⁸Sr ratios. Subsequently, the mixing of the underlying seawater, with unradiogenic Sr isotope compositions and normal δ⁸⁸Sr ratios, probably caused gradual decrease of the ⁸⁷Sr/⁸⁶Sr ratios of the seawater and deposition of carbonate with normal δ⁸⁸Sr ratios. The combination of ⁸⁷Sr/⁸⁶Sr and δ⁸⁸Sr isotope systematics gives us new insights on the surface evolution after the Snowball Earth.     

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.     

甘肃庆城庄19井区上三叠统延长组长82亚油层组 低渗透储层的地质特征

长82亚油层组是甘肃庆城地区庄19井区上三叠统延长组中储集砂岩相对富集的层位,但砂岩低渗透性的特点显著,成为影响该区石油储产量增长的主要地质因素.结合前人的相关工作,通过钻井岩心观察、测井曲线分析、储层岩石实验测试等工作,详细地分析了庄19井区长82亚油层组低渗透储层的地质特征,认为沉积微相和压实作用、胶结作用是控制低渗透性储集砂岩发育和分布的主要地质因素,寻找以水下分流河道微相为代表的有利储集相带砂岩体是油气勘探的重要方向.     

(ϖμ/ϖT) P of the lower mantle

We estimate (/T) _P of the lower mantle at seismic frequencies using two distinct approaches by combining ambient laboratory measurements on lower mantle minerals with seismic data. In the first approach, an upper bound is estimated for |(/T) _P | by comparing the shear modulus () profile of PREM with laboratory room-temperature data of extrapolated to high pressures. The second approach employs a seismic tomography constraint ( lnV _S / lnV _P ) _P =1.8–2, which directly relates (/T) _P with (K _S /T) _P . An average (K _S /T) _P can be obtained by comparing the well-established room-temperature compression data for lower mantle minerals with theK _S profile of PREM along several possible adiabats. Both (K _S /T) and (/T) depend on silicon content [or (Mg+Fe)/Sil of the model. For various compositions, the two approaches predict rather distinct (/T) _P vs. (K _S /T) _P curves, which intersect at a composition similar to pyrolite with (/T) _P =–0.02 to –0.035 and (K _S /T) _P =–0.015 to –0.020 GPa/K. The pure perovskite model, on the other hand, yields grossly inconsistent results using the two approaches. We conclude that both vertical and lateral variations in seismic velocities are consistent with variation due to pressure, temperature, and phase transformations of a uniform composition. Additional physical properties of a pyrolite lower mantle are further predicted. Lateral temperature variations are predicted to be about 100–250 K, and the ratio of ( lnp/ lnV _S ) _P around 0.13 and 0.26. All of these parameters increase slightly with depth if the ratio of ( lnV _S / lnV _P ) _P remains constant throughout the lower mantle. These predicted values are in excellent agreement with geodynamic analyses, in which the ratios ( ln / lnV _S ) _P and ( / lnV _S ) _P are free parameters arbitrarily adjusted to fit the tomography and geoid data.