桂林毛村不同植被类型土壤微生物数量与碳酸酐酶活性比较

以非岩溶区林地为对比,分析了桂林毛村岩溶区4种不同植被类型土壤微生物数量及碳酸酐酶(CA)活性的季度动态变化规律,发现以下主要结果:1随着植被的正向演替,岩溶区弃耕地、草地、灌丛及林地微生物数量及CA活性逐渐升高,微生物总数从64.07×10~4cfu/g上升到178.23×10~4cfu/g,CA活性从0.77 U/g上升到1.82 U/g,岩溶区林地大于非岩溶区林地。2在岩溶区不同植被类型,微生物组成均表现为细菌最多(平均值95.14%),放线菌次之(平均值2.79%),真菌数量最少(平均值1.75%)。而在非岩溶区表现为细菌最多(平均值90.95%),真菌次之(平均值5.32%),放线菌最少(平均值3.73%)。3微生物数量季节动态整体表现为春季至夏季逐渐上升,至秋季达到最高,冬季下降,微生物总数的增长依赖于细菌的倍数增长,真菌和放线菌影响较小。CA活性整体表现为夏季和冬季低于春季和秋季,秋季达到最大值。4 CA活性与细菌及微生物总数呈极显著的正相关,表明土壤CA主要来源于细菌的分泌。     

变渗透系数软土一维非线性固结沉降数值模拟

固结沉降计算是工程建筑中的重要内容之一。传统的固结沉降计算多是基于渗透数为常数的Terzaghi模型,这与实际的固结过程有较大的差别。采用Carman—Koze模型与一维非线性固结沉降模型进行耦合来模拟固结沉降过程。结果表明,固结导致的渗透系数的变化对固结有较大的影响,特别是在后期这种影响会越来越大。     

露天矿边坡的位移监测与滑坡预报

对湖北大冶铁矿滑坡区域的长期监测资料进行分析和总结，提出依据位移-时间曲线预报滑坡的方法。     

松辽盆地榆树林油田下白垩统泉头组扶余油层浅水三角洲沉积特征及其演化

松辽盆地榆树林油田下白垩统泉头组四段扶余油层沉积时期发育大型浅水三角洲沉积。本文基于12 口探井岩心与
2268 口钻井资料,通过单井岩心相分析、测井相分析、连井相对比和平面沉积微相研究,认为研究区发育浅水三角洲平原、
内前缘、外前缘和前三角洲亚相,以浅水三角洲平原亚相为主,平原分流河道和内前缘水下分流河道为主要沉积微相。在
扶三段（F Ⅲ）早期,研究区主要为浅水三角洲内前缘亚相,物源只来自北部 ;其后,三角洲向南进积,全区变为平原亚
相 ;F Ⅲ 3 小层沉积时期,南部物源进入,并与北部物源交汇,一直持续至扶一段（F Ⅰ）末期;在 F Ⅰ 3 小层沉积末期,湖
平面快速上升,南北两个三角洲退积,研究区中部依次出现浅水三角洲内前缘、外前缘和前三角洲。     

水泥-粉煤灰浆液在水电站隧洞灌浆中的应用

针对三叉水电站引水隧洞Ⅳ标段围岩地质条件,详细分析了水泥-粉煤灰浆液在该工程引水隧洞灌浆中的应用情况。从应用情况综合分析可以得出,隧洞灌浆采用水泥-粉煤灰浆液是可行的,完全能满足设计要求,在保证灌浆质量的前提下,可以降低部分施工成本,具有较好的推广应用价值。     

应用随机反演技术精细刻画河道砂体——以大庆油田萨北开发区萨二组为例

以大庆油田萨北开发区萨二组为例,研究了随机地震反演技术及其对河道砂体的精细刻画。研究表明:纵向上,不同厚度砂体的随机反演结果符合率差异较大:厚度大于3 m的砂体符合率为89.6%,厚度为2~3 m的砂体符合率为79.1%,厚度小于2 m的砂体符合率为71.5%;平面上,各沉积单元平均的砂体符合率能达到75%以上,且分流平原亚相的符合率要高于内前缘亚相。地震、测井及地质资料的充分结合,能够对河道的走向、复合河道砂体的单一河道边界及井间砂体叠置关系精细刻画,显示了井震结合预测河道砂体的适用性。     

Adsorption and Desorption of Phosphate on Calcite and Aragonite in Seawater

The adsorption and desorption of phosphate on calcite and aragonite were investigated as a function of temperature (5–45 °C)and salinity (0–40) in seawater pre-equilibrated with CaCO₃. An increase in temperature increased the equilibrium adsorption; whereas an increase in salinity decreased the adsorption. Adsorption measurements made in NaCl were lower than the results in seawater. The higher values in seawater were due to the presence of Mg²⁺ and Ca²⁺ ions. The increase was 5 times greater for Ca²⁺ than Mg²⁺. The effects ofCa²⁺ and Mg²⁺ are diminished with the addition of SO₄ ^2- apparently due to the formation of MgSO₄ and CaSO₄ complexes in solution and/or SO₄ ^2- adsorption on the surface of CaCO₃. The adsorbed Ca²⁺ and Mg²⁺ on CaCO₃ (at carbonate sites) may act as bridges to PO₄ ^3- ions. The bridging effect of Ca²⁺is greater than Mg²⁺ apparently due to the stronger interactions of Ca²⁺ with PO₄ ^3-.The apparent effect of salinity on the adsorption of PO₄ was largely due to changes in the concentration of HCO₃ ^- in the solutions. An increase in the concentration of HCO₃ ^- caused the adsorption of phosphate to decrease, especially at low salinities. The adsorption at the same level of HCO₃ ^- (2 mM) was nearly independent of salinity. All of the adsorption measurements were modeled empirically using a Langmuir-type adsorption isotherm[ [PO₄]_ad = K_mC_m[PO₄]_T/(1 +K_m [PO₄]_T) , ]where [PO₄]_ad and [PO₄]_T are the adsorbed and total dissolved phosphate concentrations, respectively. The values of C_m (the maximum monolayer adsorption capacity, (mol/g) and K_m (the adsorption equilibrium constant, g/(mol) over the entire temperature (t, °C) and salinity (S) range were fitted to[ C_m = 17.067 + 0.1707t - 0.4693S + 0.0082S² ( = 0.7) ][ ln K_m = - 2.412 + 0.0165t - 0.0004St - 0.0008S² ( = 0.1) ]These empirical equations reproduce all of our measurements of[PO₄]_ad up to 14 mol/g and within ±0.7 mol/g.The kinetic data showed that the phosphate uptake on carbonate minerals appears to be a multi-step process. Both the adsorption and desorption were quite fast in the first stage (less than 30 min) followed by a much slower process (lasting more than 1 week). Our results indicate that within 24 hours aragonite has a higher sorption capacity than calcite. The differences between calcite and aragonite become smaller with time. Consequently, the mineral composition of the sediments may affect the short-term phosphate adsorption and desorption on calcium carbonate. Up to 80 % of the adsorbed phosphate is released from calcium carbonate over one day. The amount of PO₄ left on the CaCO₃ is close to the equilibrium adsorption. The release of PO₄ from calcite is faster than from aragonite. Measurements with Florida Bay sediments produced results between those for calcite and aragonite. Our results indicate that the calcium carbonate can be both a sink and source of phosphate in natural waters.     

The stability of Foundation Rock in Gezhouba Project

The results of the stability study of dam foundation , including the effects of ground stresses on the stability of base masses and long-term stability and strength of weak intercalations , especially of clayey ones, are presented. It is proved that the considerable tectonic stresses exist even in red rock layers with slight folds and a gentle terrain and that the stability of masses are directly affected by local stress relief. It is found that sedimentary rock behaves like rheology. A method of deter-mining long-term strength of rheological rock is suggested.     

SiO2-TiO2薄膜制备及其光催化性能研究

Sol-gel法制备SiO2-TiO2复合薄膜，进行甲醛的光催化降解实验，研究了SiO2掺杂量、薄膜焙烧温度、甲醛溶液pH值及初始浓度对光催化性能的影响。结果表明，500℃焙烧1h，掺杂质量SiO2：TiO2=12：100时，SiO2-TiO2薄膜的光催化活性最高，150min后甲醛降解率达76％，是单纯TiO2薄膜的1．3倍，该薄膜稳定性较好，经重复8次使用，最大降解率只下降4％。