中国东北依兰地区块状蓝片岩的地球化学特征

黑龙江省依兰地区分布的黑龙江杂岩被认为足具有缝合带性质的构造混杂岩,其中所含变基性火山熔岩中含有的变质矿物不具有定向组构特征,因此称之为块状蓝片岩.特征变质矿物--蓝闪石的大量出现表明其经历过高压低温变质作用.常量地球化学分析表明,其SiO2含量均在53%以下,TiO2含量超过2%,Na2O K2O的含量为2.77%～6.41%,Na2O的含量普遍大于K2O的含量,Na2O K2O-SiO2变异图显示其具有碱性玄武岩特征;痕量元素地球化学分析显示其轻重稀土元素分异明显,稀土元素配分曲线表现为轻稀土元素富集、重稀土元素亏损的右倾型.球粒陨石标准化图解中,不具有Eu的负异常;Nbx2-Zr/4-Y、Ti/100-Zr-Sr/2与Ba-Th-Nb-La图解的综合分析表明,块状蓝片岩具有碱性洋岛玄武岩(OIB)的特征,它们应是佳木斯地块与松嫩地块之间古洋壳俯冲过程的残留,这为探讨佳木斯陆块与松嫩陆块之间古老洋盆俯冲消减过程提供了重要依据.     

鄱阳湖泥沙来源及湖盆近期沉积规律探讨

本文依据汇入鄱阳湖的河流泥沙资料和湖区泥沙淤积调查研究的成果,对鄱阳湖泥沙来源及湖盆近期沉积规律进行了探讨。赣、抚、信、饶、修五河及其区间来水挟带的泥沙是鄱阳湖泥沙的主要来源。通过沙量平衡计算:多年平均入湖沙量2310.9万吨,平均出湖沙量1179.7万吨,平均淤积量1131.2万吨。若平铺在面积为4646.64km~2的湖盆上,淤积速率为1.6mm/a。淤积部位主要是五河入湖的扇形三角洲前缘。从沉积环境的演变观点看,今后湖盆泥沙淤积有逐渐加重的趋势。     

Analysis of medaka cytochrome P450 3A homotropic and heterotropic cooperativity

We have previously demonstrated that medaka CYP3A is associated with metabolism of several endobiotics including steroids and bile acids. In this study, we demonstrate that medaka CYP3A catalysis exhibits unusual kinetic behaviors consistent with allosteric interaction which cannot be described by hyperbolic kinetic models. Using 7-benzyloxy-4-(trifluoromethyl)-coumarin (BFC) and nonylphenol as CYP3A substrates, we describe both homotropic and heterotropic cooperative interactions. Given the role of CYP3A in maintaining the homeostatic balance for numerous endobiotics, enzymatic activation/inhibition by endocrine disruptors (EDCs) represents a putative (non-genomic) mechanism for endocrine disruption.     

一类序同态的构造

作者定义了从L_1~X到L_2~Y的映射σ,证明了σ是满足σ(x_λ~0)=σ(λ)∧σ(x_(I_1)~0)的保并映射的充要条件是σ(A)=∨g(λ)∧f(Aλ),其中f为X到L_1~Y的映射,g为L_1到L_2~Y的保并映射,且有f(X)≤g(I_1);最后证明了一类序同态的分解定理,它们是前人相应结果的推广与补充。     

基于普通摄像机成像系统测量的误差分析

在人机工程学及物体、人体运动信息检测系统的研究中，较多地应用了基于普通摄像机的三维摄像测试分析系统。分析了系统基本构成原理和公式推导及实验过程中的误差来源，并对改进各种误差的方法进行了初步的探讨。     

黑龙江省东部桦南隆起美作花岗岩的锆石U-Pb定年及其地质意义

为查明马家街群发生接触变质作用的时代及其构造背景,对出露于黑龙江省东部桦南隆起的美作花岗岩体进行了锆石LA-ICP-MS U-Pb定年研究.结果显示:锆石具有清晰的生长振荡环带,其Th/U比值为0.12～1.04,属于典型的岩浆成因锆石;获得的206Pb/238U加权平均年龄为(259.0±3.6) Ma(n=14,MSWD=5.9),代表了岩体结晶年龄.美作岩体与佳木斯地块南部的青山、楚山和柴河岩体形成时代一致,其轻稀土富集、重稀土亏损型式和Eu负异常以及明显的Nb、Ta、Sr、Ti亏损的特点显示为壳源成因的火山弧花岗岩;它们的形成可能与晚古生代古亚洲洋的消减作用有关,该期花岗岩的就位导致马家街群发生了接触变质作用.美作花岗岩体形成时代的厘定,不仅限定了马家街群的变质时代为晚二叠世,同时为进一步探讨佳木斯地块晚古生代构造演化提供了新证据.     

Biogeochemical cycles of carbon, sulfur, and free oxygen in a microbial mat

Complete budgets for carbon and oxygen have been constructed for cyanobacterial mats dominated by Microcoleus chthonoplastes from the evaporating ponds of a salt works located in Guerrero Negro, Baja California Sur, Mexico. Included in the budget are measured rates of O2 production, sulfate reduction, and elemental exchange across the mat/brine interface, day and night, at various temperatures and times of the year. We infer from this data the various sinks for O2, as well as the sources of carbon for primary production. To summarize, although seasonal variability exists, a major percentage of the O2 produced during the day did not diffuse out of the mat but was used within the mat to oxidize both organic carbon and the sulfide produced by sulfate reduction. At night, most of the O2 that diffused into the mat was used to oxidize sulfide, with O2 respiration of minor importance. During the day, the internal mat processes of sulfate reduction and O2 respiration generated as much or more inorganic carbon (DIC) for primary production as diffusion into the mat. Also, oxygenic photosynthesis was the most important process of carbon fixation, although anoxygenic photosynthesis may have been important at low light levels during some times of the year. At night, the DIC lost from the mat was mostly from sulfate reduction. Elemental fluxes across the mat/brine interface indicated that carbon with an oxidation state of greater than zero was taken up by the mat during the day and liberated from the mat at night. Overall, carbon with an average oxidation state of near zero accumulated in the mat. Both carbon fixation and carbon oxidation rates varied with temperature by a similar amount. These mats are thus closely coupled systems where rapid rates of photosynthesis both require and fuel rapid rates of heterotrophic carbon oxidation.     

Sulfur isotope fractionation during bacterial sulfate reduction in organic-rich sediments

Isotope fractionation during sulfate reduction by natural populations of sulfate-reducing bacteria was investigated in the cyanobacterial microbial mats of Solar Lake, Sinai and the sediments of Logten Lagoon sulfuretum, Denmark. Fractionation was measured at different sediment depths, sulfate concentrations, and incubation temperatures. Rates of sulfate reduction varied between 0.1 and 37 micromoles cm-3 d-1, with the highest rates among the highest ever reported from natural sediments. The depletion of 34S during dissimilatory sulfate reduction ranged from 16% to 42%, with the largest 34S-depletions associated with the lowest rates of sulfate reduction and the lowest 34S-depletions with the highest rates. However, at high sulfate reduction rates (>10 micromoles cm-3 d-1) the lowest fractionation was 20% independent of the rates. Overall, there was a similarity between the fractionation obtained by the natural populations of sulfate reducers and previous measurements from pure cultures. This was somewhat surprising given the extremely high rates of sulfate reduction in the experiments. Our results are explained if we conclude that the fractionation was mainly controlled by the specific rate of sulfate reduction (mass cell-1 time-1) and not by the absolute rate (mass volume-1 time-1). Sedimentary sulfides (mainly FeS2) were on average 40% depleted in 34S compared to seawater sulfate. This amount of depletion was more than could be explained by the isotopic fractionations that we measured during bacterial sulfate reduction. Therefore, additional processes contributing to the fractionation of sulfur isotopes in the sediments are indicated. From both Solar Lake and Logten Lagoon we were able to enrich cultures of elemental sulfur-disproportionating bacteria. We suggest that isotope fractionation accompanying elemental sulfur disproportionation contributes to the 34S depletion of sedimentary sulfides at our study sites.