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首页> 外文期刊>Geochimica et Cosmochimica Acta: Journal of the Geochemical Society and the Meteoritical Society >POREWATER PH AND AUTHIGENIC PHASES FORMED IN THE UPPERMOST SEDIMENTS OF THE SANTA BARBARA BASIN
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POREWATER PH AND AUTHIGENIC PHASES FORMED IN THE UPPERMOST SEDIMENTS OF THE SANTA BARBARA BASIN

机译:圣塔巴拉巴拉盆地上层沉积物中的PH和自生相

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In this paper porewater and solid phase analyses are used in combination with in situ O-2 and pH microelectrode measurements to characterize early diagenetic processes in the uppermost sediments of the Santa Barbara Basin, California. Rapid reduction of dissolved oxygen, nitrate, solid phase manganese and iron, and dissolved sulfate is observed. Between sediment depths of 0 and 2 cm, reductive solubilization of ferric iron phases releases Fe, adsorbed phosphate, and fluoride to the porewaters and contributes to a sharp increase in porewater pH. Between 2 and 4 cm, sulfate reduction rates peak, pH levels off, and acid volatile sulfides and pyrite become the dominant forms of solid phase iron. Saturation state calculations, which depend largely on pH, indicate that the porewaters of the Santa Barbara Basin become saturated with respect to carbonate fluorapatite and calcite within the first 0.25 mm of the sediment and are highly supersaturated by and below 2 cm. In spite of this result, porewater evidence of phosphate and fluoride removal into a solid phase is observed only in the first similar to 5 cm of some cores, whereas dissolved Ca profiles suggest dispersed calcite precipitation throughout the sediment column. This finding is interpreted as an indication of the nonsteady state nature of the surface reactions that may, given sufficient nucleation sites and time, lead to carbonate fluorapatite genesis in anoxic sediments. Finally, microelectrode pH profiles from two other basins in the California Borderlands are presented. These demonstrate that the porewaters of the Santa Barbara Basin are more alkaline than those of other basins. This outcome is attributed to the lack of particle mixing and a unique interplay between Fe liberation and FeS precipitation reactions in the Santa Barbara Basin. [References: 72]
机译:在本文中,孔隙水和固相分析与原位O-2和pH微电极测量结合使用,以表征加利福尼亚州圣塔芭芭拉盆地最上部沉积物中的早期成岩作用。观察到溶解氧,硝酸盐,固相锰和铁以及溶解硫酸盐的快速还原。在0至2 cm的沉积物深度之间,三价铁相的还原性增溶将Fe,吸附的磷酸盐和氟化物释放到孔隙水中,并导致孔隙水pH值急剧增加。在2至4厘米之间,硫酸盐还原速率达到峰值,pH值稳定,酸性挥发性硫化物和黄铁矿成为固相铁的主要形式。饱和状态的计算主要取决于pH值,这表明圣塔芭芭拉盆地的孔隙在沉积物的前0.25 mm内相对于碳酸盐氟磷灰石和方解石已变得饱和,并且高度过饱和且在2 cm以下。尽管有此结果,但仅在与某些岩心5 cm相似的区域内,才观察到孔隙水将磷酸盐和氟化物去除成固相的证据,而溶解的Ca剖面表明方解石沉淀遍布整个沉积物柱。这一发现被解释为表面反应的非稳态性质的指示,在足够的成核位置和时间下,表面反应可能导致缺氧沉积物中碳酸盐氟磷灰石成因。最后,介绍了加州边境地区另外两个盆地的微电极pH分布。这些表明圣巴巴拉盆地的孔隙水比其他盆地的孔隙水更具碱性。这一结果归因于圣塔芭芭拉盆地中缺乏颗粒混合以及铁的释放与FeS沉淀反应之间的独特相互作用。 [参考:72]

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