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首页> 外文期刊>Geochimica et Cosmochimica Acta: Journal of the Geochemical Society and the Meteoritical Society >Indium and yttrium in North Atlantic and Mediterranean waters: Comparison to the Pacific data
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Indium and yttrium in North Atlantic and Mediterranean waters: Comparison to the Pacific data

机译:北大西洋和地中海水域中的铟和钇:与太平洋数据的比较

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Vertical profiles of dissolved indium and yttrium were determined in the eastern North Atlantic and the Mediterranean Sea to compare with those of the North Pacific reported earlier. The Y concentrations in the surface waters are 120 pmol/kg in the North Atlantic and 205 pmol/kg in the Mediterranean Sea, which are significantly higher than 80 pmol/kg in the North Pacific. The difference may be attributable to the different strength of input of Y to the oceans from fluvial and aeolian sources. In contrast, the deep water concentration of Y increases in the order of North Atlantic < Mediterranean < North Pacific. This trend is similar to that of dissolved Si, suggesting that Y is involved in the biogeochemical regeneration cycle. The vertical profiles of In are far more complex than Y. The In profile shows a systematic increase from 0.6 pmol/kg at the surface to 1.7 pmol/kg at 2100 m in the North Atlantic, whereas it is almost featureless at a mean concentration of 3.8+-0.6 pmol/kg in the Mediterranean Sea. The North Atlantic and Mediterranean In concentrations are considerably higher than those observed in the North Pacific (approx 0.1 pmol/kg), and such a large interoceanic variation has been reported before only for Al and Ga. Like Al, the deep water In concentration that decreases in the order of Mediterranean > North > North Pacific exhibits an inverse trend of Y and nutrients. Indium is highly particle-reactive (47% association in the Mediterranean Sea), and must have a short mean oceanic residence time. However, the featureless dissolved In profile in the Mediterranean Sea is clearly different from the profiles of dissolved Al, showing increase with depth (Hydes et al., 1998; Measures and Edmond, 1998), suggesting that significant fractionation of the two elements is taking place in the ocean. The interoceanic variations of dissolved In and Al may be ascribed to the different intensities of external input of which aeolian has been considered to be major rather than fluvial. However, the difference of In and Al concentrations in the deep waters of the above oceanic basins are significantly greater than those of other refractory elements, such as Ce, Ti, Hf, and Zr, whose major sources to the ocean are also considered to be aeolian. Furthermore, the In/Al ratios in seawater are about two orders of magnitude greater than the average crustal ratio. Thus, some additional sources, though not yet certain, may be required to explain the high concentrations of In in the Atlantic and the Mediterranean deep waters.
机译:确定了北大西洋东部和地中海中溶解的铟和钇的垂直剖面,以与早先报道的北太平洋的垂直剖面进行比较。在北大西洋,地表水中的Y浓度为120 pmol / kg,在地中海中为205 pmol / kg,明显高于北太平洋的80 pmol / kg。差异可能归因于来自河流和风成源的Y向海洋的输入强度不同。相反,Y的深水浓度按北大西洋<地中海<北太平洋的顺序增加。这种趋势类似于溶解的硅的趋势,表明Y参与了生物地球化学的再生周期。 In的垂直剖面远比Y复杂得多。In剖面显示出从系统表面的0.6 pmol / kg到北大西洋2100 m的1.7 pmol / kg的系统增加,而在平均浓度为时几乎没有特征。在地中海地区为3.8 + -0.6 pmol / kg。北大西洋和地中海地区的In浓度明显高于北太平洋地区的浓度(约0.1 pmol / kg),以前只有Al和Ga被报道有如此大的海洋变化。降序依次为地中海>北>北太平洋,其Y和养分含量呈反比趋势。铟具有很高的颗粒反应性(在地中海中为47%的缔合体),并且必须具有较短的平均海洋停留时间。但是,地中海中无特征的溶解In轮廓明显不同于溶解的Al轮廓,表现出随深度增加的趋势(Hydes等,1998; Measurement和Edmond,1998),这表明这两种元素的分馏作用正在逐步加大。放置在海洋中。溶解的In和Al的海洋变化可能归因于外部输入的不同强度,其中风成被认为是主要的而不是河流的。但是,上述大洋盆地深水中的In和Al浓度差异明显大于其他难熔元素,例如Ce,Ti,Hf和Zr,这些元素也是海洋的主要来源。风神。此外,海水中的In / Al比比平均地壳比大两个数量级。因此,尽管还不确定,但可能需要一些其他来源来解释大西洋和地中海深水中In的高浓度。

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