四川盆地海相三叠系硫同位素组成及其地质意义

系统整理研究了四川盆地海相三叠系硬石膏和卤水的硫同位素组成、演化特点及其地质意义。这对促进四川和全球海相三叠系硫酸盐硫同位素的研究有重要参考价值。     

镁渣配料煅烧硅酸盐水泥熟料的研究

研究了镁渣矿物组成和镁渣配料煅烧硅酸盐水泥熟料的反应动力在数和物理性能。结果表明：镁渣的主要矿物组成为γ－Ｃ２Ｓ、β－Ｃ２Ｓ、ＭｇＯ、ＣＦ、Ｃ２Ｆ、ＦｅＯ、ＣａＦ２等，并且镁渣可降低熟料形成反应表观活化能，加速熟料矿物的形成，提高熟料的强度。     

金矿床测年方法的某些进展

本文系统地阐述了国内外有关金矿床同位素定年方面的最新进展和古地磁法、天然裂变径迹法的基本原理 ,并对常用同位素定年法的适用性和局限性进行了评述     

不同氮浓度下三角褐指藻生长特性和化学组成

三角褐指藻是一类海洋单细胞硅藻,富含多不饱和脂肪酸,可以作为鱼、虾、贝等理想的饵料。而近年该藻曾多次在我国沿海海域发生暴发性增殖,给当地生态环境带来了一定的影响。为了探讨不同氮浓度对三角褐指藻生长特性和化学组成的影响,设置了低氮(44 μ mol.L-1)、中氮(880 μmol.L-1)和高氮(4 400 μmol.L-1)浓度三种处理,着重测定三角褐指藻的细胞密度、比生长率、生物量、可溶性糖、蛋白质含量和叶绿素含量等指标。结果表明,高氮浓度明显地促进了藻细胞的生长繁殖。高氮浓度下的藻细胞密度、比生长率和生物量分别比低氮浓度下的提高了 5.38 倍、0.81 倍和 2.86 倍。藻生长前期,高氮浓度和中氮浓度下的生长曲线相似,呈现一个"S"型的曲线。另外,高氮浓度下的藻细胞可溶性糖、蛋白质和叶绿素a含量分别是低氮浓度下的 2.5 倍、1.5 倍和 15 倍,说明高氮浓度促进了藻细胞化学组成的转化和积累。结果揭示,氮浓度可能是导致三角褐指藻近年在我国沿海海域发生暴发性增殖的重要因素。     

舟山潮差带海相沉积物的物理和化学特征

为舟山潮差带海相沉积物固结机理的深入研究提供物质基础,采用激光粒度仪分析了海相沉积物的粒度组成,并测试了海相沉积物的化学元素、化合物种类及其相对含量,还使用X-射线衍射技术分析了海相沉物的矿物组成。结果表明:海相沉积物含水率高、初始孔隙比大、呈流塑状,为低液限粉质黏土;活性指数为12.4,属于活动黏性土,矿物的亲水性较好;全盐含量高达9~11.2 g/kg,阳离子交换能力不强,有机质含量(5.82~12.7 g/kg)较高;pH 值为7.35~8.36,呈弱碱性,加上孔隙水中K+ ,Na+ ,Ca2+ ,Mg2+ 的存在,使得高岭石常不稳定,有向伊利石、蒙脱石或绿泥石转化的趋势。     

高清质谱解析河岸带湿地溶解有机质分子组成特征及其环境意义

河岸带湿地土壤溶解有机质(Dissolved organic matter,DOM)对陆源污染物的迁移和对河流水体富营养化进程均具有重要影响.本研究以典型河口冲积岛——崇明岛河岸带湿地DOM为研究对象,采用液相四级杆飞行时间质谱(Liquid chromatography quadrupole time-of-flight mass spectrometry,LC-Q-TOF-MS)技术分析河岸带湿地土壤DOM的分子组成特征,探究河岸带湿地DOM可能的主要来源.研究结果表明:LC-QTOF-MS技术成功地解析了复杂混合物DOM的分子组成特征,其中脂类化合物是崇明岛河岸带湿地土壤DOM的主要组分,占到28.87%~43.87%,其次为蛋白类物质和羰基类化合物,分别占到总DOM的17.46%~36.54%和19.13%~31.28%,最少的是脂肪酸类、糖类和氨基酸类物质,其三者之和仅为12%左右.同时,崇明岛河岸带湿地DOM分子主要来源于河岸带湿地植物光合生产和陆上区域农业面源径流、生活污水和工业废水的排放,其空间分布受小流域土地利用类型影响.研究结果为复杂混合物的分子组成解析和河岸带湿地管理提供一种新思路.     

Response of stable carbon isotope in epilithic mosses to atmospheric nitrogen deposition

Epilithic mosses are characterized by insulation from substratum N and hence meet their N demand only by deposited N. This study investigated tissue C, total Chl and δ¹³C of epilithic mosses along 2 transects across Guiyang urban (SW China), aiming at testing their responses to N deposition. Tissue C and total Chl decreased from the urban to rural, but δ¹³C_moss became less negative. With measurements of atmospheric CO₂ and δ¹³CO₂, elevated N deposition was inferred as a primary factor for changes in moss C and isotopic signatures. Correlations between total Chl, tissue C and N signals indicated a nutritional effect on C fixation of epilithic mosses, but the response of δ¹³C_moss to N deposition could not be clearly differentiated from effects of other factors. Collective evidences suggest that C signals of epilithic mosses are useful proxies for N deposition but further works on physiological mechanisms are still needed.     

STABLE ISOTOPE CHARACTERIZATION OF THE IMPACTS OF ARTIFICIAL GROUND WATER RECHARGE1

ABSTRACT: Stable isotopes of deuterium and oxygen-18 of surface and ground water, together with anion concentrations and hydraulic gradients, were used to interpret mixing and flow in ground water impacted by artificial recharge. The surface water fraction (SWF), the percentage of surface water in the aquifer impacted via recharge, was estimated at different locations and depths using measured deuterium/hydrogen (DIH) ratios during the 1992, 1993, and 1994 recharge seasons. Recharged surface water completely displaced the ground water beneath the recharge basins from the regional water table at 7.60 m to 12.16 m below the land surface. Mixing occurred beneath the recharge structures in the lower portions of the aquifer (>12.16 m). Approximately 12 m down-gradient from the recharge basin, the deeper zone (19.15 m depth) of the primary aquifer was displaced completely by recharged surface water within 193, 45, and 55 days in 1992, 1993, and 1994, respectively. At the end of the third recharge season, recharged surface water represented ～50 percent of the water in the deeper zone of the primary aquifer ～1000 m downgradient from the recharge basin. A classic asymmetrical distribution of recharged surface water resulted from the recharge induced horizontal and vertical hydraulic gradients. The distribution and breakthrough times of recharged surface water obtained with stable isotopes concurred with those of major anions and bromide in a tracer test conducted during the 1995 recharge season. This stable isotope procedure effectively quantified mixing between surface and ground water.     

荠菜叶挥发性成分分析

采用水蒸气蒸馏法对荠菜叶挥发油进行了提取。通过毛细管气相色谱—质谱联用法分离并鉴定了其化学成分,用气相色谱面积归一化法测定了各成分的相对百分含量,共分离确定了其中12种化合物,所鉴定化合物的含量占全油的65.62%,主要化学成分为：L-胍基琥珀酰亚胺（21.28%）、植醇（18%）、植酮（9.6%）、油酸（4.71%）、棕榈酸（3.97%）等。     

利用稳定同位素202Hg稀释技术判定不同来源有机肥施用对外源汞在土壤中形态分布的影响

有机肥施入土壤后,是否会对土壤重金属的活性及植物吸收造成影响是人们关心的问题.本研究应用稳定同位素²⁰²Hg稀释技术,通过培养实验和改进的Tessier连续提取法,探索不同来源有机肥(秸秆、杨树叶、油枯、酒糟、猪粪、鸡粪)施用对外源汞在天津潮土中形态分布及有效性的影响.结果表明,在连续提取法中结合同位素²⁰²Hg稀释技术,通过同位素比值R_Hg(²⁰²Hg/²⁰⁰Hg)的变化对Hg进行形态分析,相比传统的对Hg形态直接进行含量测定,可以更精确直观地反映出Hg形态分布的变化.在潮土中加入外源²⁰²Hg和有机肥后,同位素比值R_Hg最为显著的变化集中在交换态(含水溶态)、胡敏酸结合态、富里酸结合态及有机质结合态,且不同来源有机肥对Hg形态的影响也主要集中在这部分形态,对碳酸盐结合态、铁锰氧化物结合态和残渣态的影响较小.与未加入有机肥的对照处理相比,猪粪及鸡粪的施用使外源示踪²⁰²Hg显著向活性较强的交换态(含水溶态)、富里酸结合态转移,而在胡敏酸结合态中比例降低,下降幅度约为55%(猪粪)和58%(鸡粪).油枯及酒糟的施用,使外源示踪²⁰²Hg显著向活性较低的胡敏酸结合态转移,其同位素比值R_Hg分别增长了约90%(酒糟)和85%(油枯),而在活性较高的交换态(含水溶态)和富里酸结合态中分布比例降低.秸秆和杨树叶对于污染土壤Hg形态分布的影响并不显著.研究结果表明,不同来源的有机肥对Hg污染潮土中Hg的形态分布有显著影响,因此,在Hg污染农田土壤上施用有机肥料需要格外谨慎.