As a kind of marine organic matter with important geochemical characteristics, amino sugars can effectively reflect the source, diagenetic state and mineralization process of organic matter by their concentration and composition in marine environment. This article systematically concluded the research progresses of amino sugars from the aspects of their source, composition and distribution characteristics in marine environment, and the role as a biomarker indicating source and diagenetic state of marine organic matter. The result showed that the macromolecular morphology, the oxygen and nutrient level and the sedimentary environment could affect the reactivity of amino sugars. The higher ratios of glucosamine to galactosamine (GlcN/GalN) and the Total Hydrolysable Amino Acids to Total Hydrolysable Amino Sugars (THAA/THAS) can reflect the fresh planktonic organic matter source and the lower ratios can reflect the conversion from planktonic to bacterial organic matter. The carbon and nitrogen normalized yield of total hydrolysable amino sugars, however, could give contradictory results depending on the relative contribution of the source and degradation degree of organic matter. Muramic acid is suitable to estimate the contribution of relatively fresh bacteria organic matter to particulate and sediment organic matter, but it is not suitable for applying in the dissolved organic matter because of its very low concentration leading from its rapid recycle. It is critical to enhance the research on the contribution of different microorganisms to amino sugars and differentiate the influence of organic matter source and degradation on amino sugars in marine environment. The research on the conversion and fate of amino sugars in marine environment is also needed. 相似文献
In the UK there is a longstanding interest in the Cl content of coals because of the adverse effects associated with high-Cl coals during combustion. An average Cl content of a representative suite of coal samples is 0.44 wt.%, but the range is from near zero to over 1%. Several lines of evidence show that in the high-Cl coals the Cl is associated with the coal moisture and that other sources, such as the silicate minerals, are negligible. Although the Cl is moisture associated there is anion exchange with the organic matter, which means that Cl is less than 100% water- soluble unless the Cl is exchanged with other anion species. This occurs if carbonates are present and calcite in particular. The Cl and Br are closely related and the location within the coal is thought to be common to both. These two elements differ from nearly all other trace elements in UK coals in that they are not present in significant concentrations in the mineral matter or bound within the organic matter. Whereas there is a good understanding of the geochemical behaviour of these other elements this is not the case for Cl and Br in the coal moisture. Chlorine and Br are thought to be conservative elements in the diagenetic evolution of the porewaters, in which an original marine depositional imprint could have been preserved. In some areas the porewaters may have fully evolved pre-Permian, whereas in other areas the diagenetic evolution could be much longer. 相似文献
Blake Ridge hosts an extensive gas hydrate system where escaping CH4 is consumed through anaerobic oxidation of methane (AOM) at a sulfate–methane transition (SMT) in shallow sediment. Previous geochemical work on ridge crest sediment has documented Ba fronts above the SMT, and has suggested that these horizons can be used to constrain the evolution of the SMT and AOM over time. We expand on this concept and further test it by determining the labile Ba contents of sediment and the dissolved Ba2+ concentrations of pore waters at four ODP sites on Blake Ridge (on the crest at Sites 994, 995 and 997, and on the southern flank at Site 1059). Labile Ba contents are fairly low at all four sites (0.44 and 1.32 mmol/kg), except within 3 m above the SMT at Sites 994, 995 and 997, where they typically exceed 1.24 mmol/kg and can reach 11.3 mmol/kg. These Ba fronts have a diagenetic origin, and SEM analyses show them to be composed of microcrystalline barite. Site 1059 lacks a prominent Ba front. The lowest labile Ba contents generally underlie the Ba fronts and correlate to the base of the SMT. Dissolved Ba2+ concentrations are low (< 1–4 μM) from the seafloor to within 2 m above the main Ba front. Below this depth, they rapidly increase at Sites 994, 995, and 1059, reaching peak concentrations (to 57 μM) at the base of the SMT. By contrast, a rapid rise in dissolved Ba2+ is not observed at Site 997. Dissolved Ba2+ concentrations are only moderately high (10–25 μM) below the SMT at all four sites. Collectively, this information supports a diagenetic model where barite passing into the SMT dissolves, and some of the dissolved Ba2+ then migrates up to form an authigenic barite peak. The contrasting signatures at the different sites indicate non-steady-state differences in the overall process. The size of the peaks on the crest of Blake Ridge necessitates that the recycling of Ba across the SMT has been operating at the current sub-bottom depths for > 100 kyr. Thus, CH4 escaping through the AOM has likely been fairly constant over this time. It is possible that the SMT is currently rising toward the seafloor at Site 1059. 相似文献
Retention ponds have been dug along some of the motorways in France to minimize environmental pollution by keeping pollutants
from spreading over the surrounding area. In the current work, eight core samples were collected from the bottom of a retention
pond located along the A-71 motorway in Sologne to study the pollution of sediment by heavy metals and their diagenetic behaviour.
The vertical concentration profiles of metals (Pb, Zn, Cd, Fe and Mn) in sediment as well as in interstitial water were determined.
Especially in the case of the sediment, a sequential extraction method was employed to investigate how the movement of each
metal is associated with the other metals and with other solid phases such as organic matter. In addition, to investigate
the relative mobility of the metals, the distribution coefficients (KD) were also determined. The concentrations of the metals were always found to be highest in the topmost layer of sediment.
This so-called surface enrichment is caused by a substantial increase of the non-detrital fraction of these metals at the
sediment surface. For instance, the accumulation of Pb and Zn is associated with the increase in the "fraction II" in the
sequential extraction. The accumulation of Cd at the surface (0–2 cm) is partly due to the liberation of Cd from the particles
during early diagenesis. However, the major factor contributing to the accumulation of Cd at the sediment surface is attributed
to the dissolution of Cd from polluted roadside soil during the periods of rainstorms and its subsequent redeposition on the
sediment surface after being carried to the retention pond. KD values for Zn and Cd were found to decrease with depth, while KD values for Pb increased. Based on the KD values, the relative mobilities of the studied metals were determined to be as follows: Mn>Zn>Cd>Pb, for the upper layer,
and Mn>Cd>Zn>Pb, for the layers below.
Received: 28 October 1996 / Accepted: 21 November 1996 相似文献
Ground‐based hyperspectral imaging combined with terrestrial lidar scanning is a novel technique for outcrop analysis, which has been applied to Early and Late Albian carbonates of the Pozalagua Quarry (Cantabrian Mountains, Spain). An image processing workflow has been developed for differentiating limestone from dolomite, providing additional sedimentary and diagenetic information, and the possibility to quantitatively delineate diagenetic phases in an accurate way. Spectral absorption signatures can be linked to specific sedimentary or diagenetic products, such as recent and palaeokarst, hydrothermal karst, (solution enlarged) fractures and different dolomite types. Some of the spectral signatures are related to iron, manganese, organic matter, clay and/or water content. Ground‐truthing accessible parts of the quarry showed that the classification based on hyperspectral image interpretation was very accurate. This technique opens the possibility for quantitative data evaluation on sedimentary and diagenetic features in inaccessible outcrops. This study demonstrates the potential of ground‐based imaging spectroscopy to provide information about the chemical–mineralogical distribution in outcrops, which could otherwise not be established using conventional field methods. 相似文献
A three-dimensional computer model is presented for studying the interaction of heat and mass transport regarding the temporal
and spatial evolution of sandstones. The model simulates coupled heat and reactive mass transport in porous rocks. In general,
mineral solubilities in water are low. Therefore, large fluid volumes are required to flow through the rock to explain observed
mineral cements in sandstones. Besides mass transport, pore fluids transport heat which modifies rock temperatures. Very high
flow rates result in strong temperature modifications and, therefore, enhance diagenesis. Low flow rates often cannot account
for observed cementation. The model results show the effect of advective, convective and conductive heat transport on temperature
and diagenetic evolution of sandstones for two different flow systems in a simple geological environment.
Received: 6 August 1996/Accepted: 18 December 1996 相似文献