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Chromophoric dissolved organic matter (CDOM) in the Equatorial Atlantic Ocean: Optical properties and their relation to CDOM structure and source

机译:赤道大西洋的发色溶解性有机物(CDOM):光学性质及其与CDOM结构和来源的关系

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Extensive data exist on the optical properties of CDOM from terrestrial and coastal environments, yet the open oceans have been historically under-sampled. Consequently, the source and structural basis of marine CDOM optical properties are still debated. To address this issue, detailed optical measurements were acquired for both untreated and sodium borohydride (NaBH_4) reduced natural waters and C18 extracts (C18-OM) across the Equatorial Atlantic Ocean. Except in regions of upwelling or in the vicinity of the Congo River outflow, CDOM absorption coefficients and visible emission intensity were far smaller for surface waters (a_(CDOM)(355): 0.057-0.162 m~(-1); λ_(ex)/λ_(em) = 350/450 nm: 0.396-1.431 qse) than for waters below the mixed layer (a_(CDOM)(355) 0.084-0.344 m~(-1); λ_(ex)/λ_(em) = 350/450 nm: 0.903-3.226 qse), while spectral slopes were higher (surface: 0.019 to 0.025 nm~(-1); deep: 0.013 to 0.019 nm~(-1)), consistent with photobleaching of CDOM in surface waters. Distinct emission bands were observed in the ultraviolet, primarily at excitation/emission wavelengths (λ_(ex)/λ_(em)) = 280/ 320 nm, but also at λ_(ex)/λ_(em)= 300/340,300/405 and 320/380 nm for some stations and depths. In contrast, visible emission exhibited maxima that continuously redshifted with increasing λ_ex(>330 nm), a property characteristic of CDOM from estuarine and coastal environments. Further evidence that CDOM in the offshore waters of this region is composed of a major terrestrial component includes: 1) similar spectral dependencies of the emission maxima and fluorescence quantum yields; 2) a large Stokes shift in the emission maxima with short-wavelength excitation (λ_ex = 280 nm); 3) correlation of visible emission intensities with absorption at λ_ex = 280,320 and 450 nm, with absorption to fluorescence ratios comparable to those found in estuarine and coastal environments; 4) affinity of C18 cartridges for the long wavelength (visible) absorbing and emitting material, but not the UV emitting material; 5) preferential loss of visible absorption and substantially enhanced blue-shifted emission in the visible following borohydride reduction of both the Equatorial Atlantic waters and the C18-OM of these waters. These results support the occurrence in offshore waters of a major terrestrial CDOM component that absorbs in the UV and visible and emits in the visible, as well as marine CDOM components that absorb and emit in the UV. The results further demonstrate that the simultaneous acquisition of complete spectral absorption and emission properties, combined with chemical tests (C-18 extractions, borohydride reduction) can provide a far clearer picture of the sources and cycling of CDOM within the oceans.
机译:存在来自陆地和沿海环境的有关CDOM光学特性的大量数据,但从历史上看,对开放海洋的采样不足。因此,海洋CDOM光学特性的来源和结构基础仍在争论中。为了解决这个问题,在赤道大西洋上空对未经处理的硼氢化钠(NaBH_4)还原的天然水和C18提取物(C18-OM)进行了详细的光学测量。除了上流区域或刚果河流出附近,地表水的CDOM吸收系数和可见发射强度要小得多(a_(CDOM)(355):0.057-0.162 m〜(-1);λ_(ex )/λ_(em)= 350/450 nm:0.396-1.431 qse)比混合层以下水域(a_(CDOM)(355)0.084-0.344 m〜(-1);λ_(ex)/λ_(em )= 350/450 nm:0.903-3.226 qse),而光谱斜率更高(表面:0.019至0.025 nm〜(-1);深:0.013至0.019 nm〜(-1)),与CDOM在光漂白中的相符地表水。在紫外线下观察到明显的发射带,主要在激发/发射波长(λ_(ex)/λ_(em))= 280/320 nm,但在λ_(ex)/λ_(em)= 300 / 340,300 / 405对于某些测站和测深来说是320/380 nm。相反,可见光发射的最大值随λ_ex(> 330 nm)的增加而连续发生红移,这是CDOM在河口和沿海环境中的特性。进一步的证据表明,该区域近海的CDOM由主要的陆地成分组成,包括:1)发射最大值和荧光量子产率的相似光谱依赖性; 2)在短波长激发下,发射最大值的斯托克斯位移大(λ_ex= 280 nm); 3)可见光发射强度与在λ_ex= 280,320和450 nm处的吸收之间的相关性,其吸收/荧光比与河口和沿海环境中的吸收比相当; 4)C18碳粉盒对长波长(可见光)吸收和发射材料的亲和力,但对紫外线发射材料的不亲和力; 5)赤道大西洋水域和这些水域的C18-OM均被硼氢化物还原后,可见光吸收的优先损失降低,可见光中蓝移的发射大大增强。这些结果支持了在海洋中吸收紫外线和可见光并在可见光中发射的主要陆地CDOM组分以及吸收和发射紫外线的海洋CDOM组分的发生。结果进一步证明,同时获得完整的光谱吸收和发射特性,再结合化学测试(C-18萃取,氢硼化物还原),可以更清楚地了解海洋中CDOM的来源和循环。

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