海水盐度对牙鲆仔稚鱼的生长、存活率及白化率的影响

１９９３年１１月２０日自鹿儿岛养殖业购得自然产卵获得的牙鲆受精卵，经空运、陆驼至福冈的九州大学附属水产试验所，仔鱼翌日孵出，３ｄ后开口。以此材料观察研究试验室条件下不同海水盐度对牙鲆仔稚鱼的生长，存活率及白化率的影响。试验分４组，盐度分别为：１组（自然海水对照组），３０．５－３１．８；２组，２６．０：３组，２１．０；４组，１６．０。每组设２个重复，使用１００１透明玻璃钢水槽，每槽放２０００尾刚开口     

Fractal-like adsorption kinetics of Pb^2＋ in rocks

The adsorption kinetics of Pb^2＋ in rocks has been studied using ion selective electrodes and atomic absorption spectrophotometer. The results showed that the adsorption process is a fractal-like reaction. The adsorption rate was relatively high before 30 minutes, and then dropped. The saturated adsorption capacity （a） of Pb^2＋ and kinetic parameters （b, a, D and k） increased with increasing initial concentrations of Pb^2＋. These parameters （except a） decreased while Na^＋ was present in the solution. Furthermore, the smaller the rocks were in grain size, the bigger these kinetic parameters would be, though the parameter a was almost constant.     

应用生烃动力学法研究川东上二叠统烃源岩生烃史

现今川东上二叠统烃源岩生烃史研究具有局限性.首先,没有对上二叠统Ⅰ-Ⅱ1型灰岩生油、Ⅲ型泥岩的生气史分开评价;其次,海相镜质组反射率通过拟合公式换算成镜质体反射率评价烃源岩成熟度具有局限性.针对上述不足,笔者通过热模拟实验,利用化学动力学方法,标定出两类源岩生油、生气的动力学参数,并结合川东地区的埋藏史及热史,模拟出源岩有机质的成烃转化率曲线.研究表明:上二叠统灰岩、泥岩有机质在距今200 Ma和190 Ma分别进入了生油、生气门限,而在距今170 Ma和140 Ma生烃结束.     

菲降解菌的降解特性及酶促反应动力学研究

通过对取自MBR膜生物反应器中的活性污泥加入菲进行富集培养、驯化,分离、纯化出一株能以菲为唯一碳源和能源的短杆状革兰氏阴性菌J-1,细菌长2～5μm,宽1～3μm;研究了初始底物浓度、温度、pH对菌株J-1降解菲的影响,探讨了菌株J-1胞内酶对菲降解的底物抑制动力学。试验表明:菌株J-1在48h内能将不同浓度菲的水溶液中的菲完全降解;菲浓度增加,达到完全降解的时间延长。温度对细菌的降解能力影响较大,菌株J-1对菲降解的最佳温度为28℃。1.15mg·L-1的菲,28℃时48h内能完全降解,而相同时间内10℃时的降解率仅为36.65%。菌株J-1对pH的波动具有一定的适应性,pH在一定范围内(6.0～8.4)变化对菲降解的影响不大,降解反应的最佳pH为7.2。菌株J-1对菲的降解符合一级动力学反应方程。较高的底物浓度对酶促降解反应具有抑制作用,酶促反应的最大速率常数vm=1.17mg·L-1·h-1,米氏常数Km=61.70mg·L-1;底物抑制常数kS=49.60mg·L-1;最佳底物浓度[S]opt=55.32mg·L-1。     

Kinetics of redox cycling of iron coupled with fulvic acid

The kinetics of conversion of iron(III) (hydr)oxides to ferrous iron mediated by fulvic acid have been investigated in order to improve the understanding of the redox cycling of iron at the oxic-anoxic boundary in natural waters. Under the conditions similar to natural waters, fulvic acid is able to reduce the iron(III) (hydr)oxide. The kinetics of the reaction depend on the reactivity of iron(III) (hydr)oxides and the reducing power of the fulvic acid. The rate of reaction is 60 nm/h obtained under following conditions: total concentration of Fe(III) 1.0 × 10^–4 M, pH 7.5, fulvic acid 5 mg/L. The rate is considered as a net result of reduction and oxidation in the > Fe^III-OH/Fe(II) wheel coupled with fulvic acid. In a real natural water system, reductants other than fulvic acid may be of importance. The results obtained in the laboratory, however, provide evidence that the Fe(OH)₃(s)/Fe(II) redox couple is able to act as an electron-transfer mediator for the oxidation of natural organic substances, such as fulvic acid by molecular oxygen either in the absence of microorganisms or as a supplement to microbial activity.     

Brønsted reactions on oxide mineral surfaces and the temperature-dependence of their dissolution rates

The pH-dependence of oxide dissolution rates is controlled by Brønsted acid-base reactions at the mineral surface. These reactions are rapid but depend explicitly on temperature, as do the subsequent slow rates of bond hydrolysis. The net result is that dissolution rates vary in a complicated fashion with temperature and solution pH. The enthalpy changes of acid-base reactions on oxide materials are sufficiently similar, however, that general statements can be made about their contribution. The enthalpy changes from proton adsorption to a hydroxyl functional group (SOH), or to a deprotonated functional group (SO ^–), are generally exothermic. The enthalpy changes become increasingly endothermic, however, as charge accumulates on the mineral surface and the charged species interact electrostatically. The result is that mineral dissolution rates are least sensitive to temperature, as measured with an Arrhenius-like rate law, at pH conditions near the Point of Zero Net Proton Charge.     

斜交型不稳定谱点分布侧半圆定理及其增长率上界的估计

本对斜交型扰动不稳定谱点的分布做了理论分析，得到了该谱点分布的半圆定理一该谱点分布在复一面上以原点为圆心以R0为半径的上半平面上，同时还对该不稳定增长率的上界作了估计。发现水平永度越小，模式顶越高则该估计值越大；垂直风切变的增大和纬度的增高对该增长率的增大有正贡献；当层结稳定度减小时，最大增长率随相对最大增长率得增大而减小。     

25～75℃酸性NaCl溶液中方铅矿的溶解动力学

在25～75℃、pH=0.43～2.45的1mol/LNaCl溶液中进行了方铅矿的溶解动力学实验。发现在远平衡条件下,方铅矿的溶解速率r与氢离子活度犤H+犦呈线性关系,溶解速率方程(速率定律)为:r=k犤H+犦,即对H+而言,溶解反应为一级。其中速率常数k为2.344×10-7mol/m2·s(25℃)、1.380×10-6mol/m2·s(50℃)、7.079×10-6mol/m2·s(75℃)。溶解反应的活化能为43.54kJ/mol,方铅矿的溶解机理为表面化学反应,速率决定步骤为表面配合物的离解。     

The presence, characteristics and earthquake implications of the St. Lawrence fault zone within and near Lake Ontario (Canada–USA)

Questions persist concerning the earthquake potential of the populous and industrial Lake Ontario (Canada–USA) area. Pertinent to those questions is whether the major fault zone that extends along the St. Lawrence River valley, herein named the St. Lawrence fault zone, continues upstream along the St. Lawrence River valley at least as far as Lake Ontario or terminates near Cornwall (Ontario, Canada)–Massena (NY, USA). New geological studies uncovered paleotectonic bedrock faults that are parallel to, and lie within, the projection of that northeast-oriented fault zone between Cornwall and northeastern Lake Ontario, suggesting that the fault zone continues into Lake Ontario. The aforementioned bedrock faults range from meters to tens of kilometers in length and display kinematically incompatible displacements, implying that the fault zone was periodically reactivated in the study area. Beneath Lake Ontario the Hamilton–Presqu'ile fault lines up with the St. Lawrence fault zone and projects to the southwest where it coincides with the Dundas Valley (Ontario, Canada). The Dundas Valley extends landward from beneath the western end of the lake and is marked by a vertical stratigraphic displacement across its width. The alignment of the Hamilton–Presqu'ile fault with the St. Lawrence fault zone strongly suggests that the latter crosses the entire length of Lake Ontario and continues along the Dundas Valley.The Rochester Basin, an east–northeast-trending linear trough in the southeastern corner of Lake Ontario, lies along the southern part of the St. Lawrence fault zone. Submarine dives in May 1997 revealed inclined layers of glaciolacustrine clay along two different scarps within the basin. The inclined layers strike parallel to the long dimension of the basin, and dip about 20° to the north–northwest suggesting that they are the result of rigid-body rotation consequent upon post-glacial faulting. Those post-glacial faults are growth faults as demonstrated by the consistently greater thickness, unit-by-unit, of unconsolidated sediments on the downthrown (northwest) side of the faults relative to their counterparts on the upthrown (southeast) side. Underneath the western part of Lake Ontario is a monoclinal warp that displaces the glacial and post-glacial sediments, and the underlying bedrock–sediment interface. Because of the post-glacial growth faults and the monoclinal warp the St. Lawrence fault zone is inferred to be tectonically active beneath Lake Ontario. Furthermore, within the lake it crosses at least five major faults and fault zones and coexists with other neotectonic structures. Those attributes, combined with the large earthquakes associated with the St. Lawrence fault zone well to the northeast of Lake Ontario, suggest that the seismic risk in the area surrounding and including Lake Ontario is likely much greater than previously believed.