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51.
Diagenesis of vascular plant organic matter components during burial in lake sediments 总被引:12,自引:0,他引:12
Diagenetic changes are difficult to distinguish from variations in sources of organic matter to sediments. Organic geochemical comparisons of samples of wood, bark, and needles from a white spruce (Picea glauca) living today and one buried for 10,000 years in lake sediments have been used to identify the effects of diagenesis on vascular plant matter. Important biogeochemical changes are evident in the aged spruce components, even though the cellular structures of the samples are well preserved. Concentrations of total fatty acids dramatically diminish; unsaturated and shorter chainlength components are preferentially lost from the molecular distributions. Concentrations of total alcohols are similar in the modern and 10,000-year-old wood and bark but markedly lowered in the aged needles. Hydrocarbon concentrations and distributions show little diagenetic change in the 10,000-year-old plant materials. Cellulose components in the wood decrease relative to lignin components, although both types of materials remain in high concentration in comparison to other organic components. Aromatization of abietic acid proceeds more rapidly in buried spruce wood than in bark; retene is the dominant polyaromatic hydrocarbon in the aged wood. In contrast to the variety of changes evident in molecular compositions, neither 13C values nor C/N ratios differ significantly in the bulk organic matter of modern and aged spruce components. 相似文献
52.
我国藻菌生物成因的金矿研究 总被引:1,自引:0,他引:1
生物成矿作用分为生物直接成矿作用和生物间接成矿作用,生物直接成矿作用的标志结构为生物有机胶体结构。生物间接成矿作用的标志结构为“矿交代生物”结构,我国陕西二台子-半仓沟金矿,四川东北寨金矿、川甘拉尔玛金矿和云南金厂金矿等均为典型为实例,矿石中普遍含有多种金属矿物生物结构,还含多种生物有机组分。成矿物质具有多源性特征,硫同位素具混合型特征,矿床成型机制可与“人工碳吸附系统”聚金机制相类比,含金层位可 相似文献
53.
A. Glabert O.S. Pokrovsky C. Reguant J. Schott A. Boudou 《Journal of Geochemical Exploration》2006,88(1-3):110
This work is devoted to the physico-chemical study of cadmium and lead interaction with diatom–water interfaces for two marine planktonic (Thalassiosira weissflogii = TW, Skeletonema costatum = SC) and two freshwater periphytic species (Achnanthidium minutissimum = AMIN, Navicula minima = NMIN) by combining adsorption measurements with surface complexation modeling. Reversible adsorption experiments were performed at 20 °C after 3 h of exposure as a function of pH, metal concentration in solution, and ionic strength. While the shape of pH-dependent adsorption edge is similar among all four diatom species, the constant-pH adsorption isotherm and maximal binding capacities differ. These observations allowed us to construct a surface complexation model for cadmium and lead binding by diatom surfaces that postulates the constant capacitance of the electric double layer and considers Cd and Pb complexation with mainly carboxylic and, partially, silanol groups. Parameters of this model are in agreement with previous acid–base titration results and allow quantitative reproduction of all adsorption experiments. 相似文献
54.
Margaret C. Graham John G. Farmer Ian W. Oliver Angus B. MacKenzie Robert M. Ellam 《中国地球化学学报》2006,25(B08):112-112
Natural uranium has three isotopes, ^238U, ^235U and ^234U, with natural abundances of 99.27 atom %, 0.72% and 0.0055%, respectively. Only ^235U is fissile and the production of nuclear fuel and nuclear weapons involves enrichment of uranium in ^235U. This process also results in separation of ^234U from ^238U, leaving depleted uranium (DU), with typical ^234U/^238U and ^235U/^238U activity ratios of about 0.19 and 0.013, respectively, as a waste product. The high density, high melting and boiling points and chemical stability of uranium and the availability of DU in relatively pure form mean that DU has many uses, including armour-piercing munitions. Such munitions have been developed in the UK since the 1960s and testing has been carried out by the Ministry of Defence (MoD) at firing ranges such as Dundrennan, SW Scotland and Eskmeals, NW England. The firing of DU munitions can result in the dispersion of DU and its combustion products (oxides) as aerosols or as larger fragments, with the potential for human exposure either directly at the site of detonation or via post-depositional migration in the environment. The aim of this work was to investigate the potential environmental mobility of DU by characterizing the associations of U in soil porewaters with increasing distance from a firing site. To this end, several soil cores located down-wind of the firing site at Dundrennan, near Kirkcudbright, SW Scotland, were collected in May 2006. These were sectioned on-site into 1- or 2-cm depth intervals and porewaters were isolated by centfifugation (10 minutes; 8873 g) on return to the laboratory. Following filtration through 0.2-micron cellulose nitrate filters, the porewaters were analyzed by ICP-QMS (U concentration) and ICP-OES (Fe, Al, Ca, Mg, Mn concentrations). Sub-samples were also subjected to centrifugal ultrafiltration (100, 30, and 3 kD) and to gel electrophoretic fractionation (agarose; 0.045 M Tris-borate; 20 mA, 30 minutes). Results showed that U was present at up to 4 μg/L in the soil porewater and that the associations of U varied with sample location and soil depth. 相似文献
55.
Daoyong ZHANG Xiangliang PAN Shuimu LIAO Chenglin HUANG Jingmei ZHANG 《中国地球化学学报》2006,25(B08):133-133
Low molecular weight organic acids (LMWOAs) are important components of root exudates. They play an important role in immobilizing and remobilizing contaminants in rhizospheric soil. Effects of four LMWOAs on the sorption and desorption behavior of p-chlorophenol by yellow earth was studied in batch mode. The results showed that the previous application of LMWOAs to enhanced adsorption capacity of p-chlorophenol of the soil in the order of maleic acid〉malic acid〉oxalic acid〉citric acid. However, when LMWOAs were applied to soil where p-chlorophenol had been previously adsorbed, substantial p-chlorophenol was desorbed from soil by oxalic acid, whereas citric acid, malic acid and maleic acid didn't desorb as much p-chlorophenol from soil as deionized water. 相似文献
56.
Fan YANG Qinghui HUANG Jianhua LI Xiaomin ZHU 《中国地球化学学报》2006,25(B08):262-262
Dissolved organic matter (DOM) is an important chemical component in natural water. Chromophoric dissolved organic matter (CDOM), a fraction of optical properties, plays art important role in the biogeochemical cycle of nutrients in aquatic environment. People realized that DOM cycle is crucial in the global carbon and nitrogen flux, and also is inherently related to nutrients and trace metal elements. Therefore, CDOM was concerned by scientists in global oceanography and limnology fields. Water samples were collected from three sections (North Channel, South Channel and Zhuyuan) of the Yangtze (Changjiang River) estuary in March 2006 Three-dimensional excitation emission matrix (3-DEEM) fluorescence spectra were analyzed for those filtrates through Whatman GF/F filters. Dissolved organic carbon (DOC) was also measured by TOC analyzer. The tidal variety was also taken into account. The 3-D EEM fluorescence scans suggested the fluorescence characteristics of humic acid (Ex=332-344 nm, Em=439-451 nm) and fulvic acid (Ex=250-254 nm, Em=472-478 nm) were obvious, and the fluorescence group of protein-like and tyrosine (Ex=230 nm, Em=283 nm) was also found. They are mainly composed of CDOM in the Yangtze estuary. Further data analysis, especially the fluorescence index (f 450/500), showed that terrestrial signal was rather strong (1.41-1.65) in the surface water, however, some terrestrial CDOM signals of bottom water showed excursions (1.28-1.39). On the other hand, anthropogenic sign was impressed in the waters of Zhuyuan, which is one of the main drain outlets of Shanghai Metropolis. DOC concentrations ranged from 2.2 mg/L to 3.4 mg/L in Zhuyuan and South Channel, and from 2.0 mg/L to 2.4 mg/L in North Channel. The tide effect played a role in the composition of the CDOM measured by 3-D fluorescence scan technology. 相似文献
57.
58.
An 11-month observation of dissolved and particulate organic matter, chlorophyll a(Chl a), C18 Sep-Pak extractable hydrophobic dissolved organic matter (hDOM) fraction and associated dissolved trace metals (Cd,
Cu, V, Co, Ni, Mo, U) was performed in the Lot–Garonne River system. This system includes the Riou Mort, the Lot River and
the downstream reaches of the Garonne River and represents the fluvial transport path of trace metals between the major point
source of polymetallic pollution, located in the Riou Mort watershed and the Gironde estuary. Spatial and temporal variations
of dissolved and particulate organic carbon and Chl areflect the presence of different types of organic matter and their relation with the hDOM fraction. Maximum Chl a/POC ratios (up to 0.03), indicate intense phytoplankton production from March to May. In the Lot River (Temple), DOC and
POC concentrations were clearly higher and mean Chl a concentration (2.8 mg g−1) was about three times higher than those of the other sites. High Chl a/POC ratios suggest high phytoplankton activity with maxima in spring and late summer. In the Riou Mort River, very high POC
concentrations of up to 40 (mean: 20) occurred, whereas Chl a concentrations were relatively low indicating low phytoplankton activity. High, strongly variable DOC and POC concentrations
suggest important natural (Carboniferous soils, forests) or anthropogenic (e.g., former coal mines, waste areas, agriculture,
sewage) carbon sources within the small Riou Mort watershed. Despite high DOC concentrations in the Riou Mort River, hDOM
metal fractions were generally lower than those at the other sites. The general order of decreasing binding strength between
metals and the organic hydrophobic phase (Cu, U > Co, Ni > V, Mo > Cd) at all four sites was in good agreement with the Irving–William
series of transition element affinity towards organic ligands. Accordingly, the role of the hydrophobic phase in dissolved
Cd transport appeared to be negligible, whereas the hDOM–Cu fraction strongly contributed to dissolved Cu transport. 相似文献
59.
旧供水井化学处理方法介绍--以加德满都市旧供水井修复为例 总被引:1,自引:0,他引:1
章伟民 《水文地质工程地质》2005,32(6):100-101,107
本文以加德满都市旧供水井修复项目为例,针对因滤水管缝隙被化学物质堵塞,导致井出水量逐年减少的旧供水井。通过井下电视摄像系统检查,采用六偏磷酸钠、氨基黄酸等有机酸,结合刷洗、高压喷射等机械方法进行处理,使旧供水井出水量得到明显提高。 相似文献
60.
Sandro Fuzzi Maria Cristina Facchini Stefano Decesari Emanuela Matta Mihaiela Mircea 《Atmospheric Research》2002,64(1-4)
We have recently set up a new procedure for characterising the water soluble organic compounds (WSOC) in fog water, for which information is still rather limited. Fog samples collected during the 1998–1999 fall–winter season in the Po Valley (Italy) were analysed following this procedure, which allows a quantitative determination of three main classes of organic compounds (neutral species, mono- and di-carboxylic acids, polycarboxylic acids), together accounting for ca. 85% of the total WSOC. This procedure also provides information on the main chemical characteristics of these three classes of compounds (functional groups, aliphatic vs. aromatic character, etc.). The enhanced chemical knowledge on fog/cloud chemical composition opens new scenarios as far as chemical and microphysical processes in clouds and fogs are concerned. 相似文献