Examining marine particulate organic matter at sub-micron scales using scanning transmission X-ray microscopy and carbon X-ray absorption near edge structure spectroscopy

被引:72
作者
Brandes, JA
Lee, C
Wakeham, S
Peterson, M
Jacobsen, C
Wirick, S
Cody, G
机构
[1] Univ Texas, Inst Marine Sci, Port Aransas, TX 78373 USA
[2] SUNY Stony Brook, Marine Sci Res Ctr, Stony Brook, NY 11794 USA
[3] Skidaway Inst Oceanog, Savannah, GA 31411 USA
[4] Univ Washington, Sch Oceanog, Seattle, WA 98195 USA
[5] SUNY Stony Brook, Dept Phys, Stony Brook, NY 11794 USA
[6] Carnegie Inst Sci, Geophys Lab, Washington, DC 20015 USA
关键词
organic geochemistry; sediment trap; X-ray microscopy; Arabian Sea; black carbon; algaenan;
D O I
10.1016/j.marchem.2004.06.020
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Marine sinking particulate organic matter (POM) represents the link between surface primary production and burial of organic matter in marine sediments. As such, the nature of this material has been the subject of numerous studies attempting to characterize its composition. The results of these studies have shown that a significant proportion of POM is not recognizable as known compounds, and that the proportion of uncharacterized material increases with age/depth/diagenesis. However, few studies have examined the spatial heterogeneity of this material. This study uses a new tool, scanning transmission X-ray microscopy (STXM), together with carbon X-ray absorption near edge structure (C-XANES), to examine POM collected from sediment traps deployed at one location in the Arabian Sea as part of the JGOFS program. The results indicate that POM is composed primarily of four distinct phases: protein, an aliphatic rich phase, a carboxylic-acid-rich phase, and a phase with complex unsaturated and quinone character. This last phase may be a condensation product between carbohydrates and proteins, or from degraded plant pigments. Many particles consisted of a single chemical phase; however, in particles with mixed compositions, individual domains retained distinctive chemical signatures at the instrument's resolution limit (50 nm). All major chemical phases were observed in sediment trap particles from 531 to 3369 m depth, supporting the hypothesis that non-selective degradation dominates particle remineralization, and that overall particle compositions are determined by near surface processes. Only one particle, out of more than 60 examined, exhibited soot-like composition. The lack of a significant black carbon/soot component may be attributable to sampling during the winter monsoon period. (C) 2004 Elsevier B.V. All rights reserved.
引用
收藏
页码:107 / 121
页数:15
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