Iron biogeochemistry in sediments on the western continental shelf of the Antarctic Peninsula

被引:8
|
作者
Burdige, David J. [1 ]
Christensen, John P. [2 ]
机构
[1] Old Dominion Univ, Dept Ocean & Earth Sci, Norfolk, VA 23529 USA
[2] New England Oceanog Lab, Brunswick, ME 04011 USA
基金
美国国家科学基金会;
关键词
Iron; Sediment diagenesis; Southern Ocean; EARLY DIAGENETIC PROCESSES; LABILE ORGANIC-MATTER; PORE-WATER; ISOTOPIC COMPOSITION; CARBON OXIDATION; MARINE SEDIMENT; SEA-ICE; MANGANESE; DISSOLUTION; COASTAL;
D O I
10.1016/j.gca.2022.03.013
中图分类号
P3 [地球物理学]; P59 [地球化学];
学科分类号
0708 ; 070902 ;
摘要
We examined iron biogeochemistry in continental margin sediments along the western side of the Antarctic Peninsula (WAP) to explore the connections between iron redox cycling and other sediment biogeochemical processes, and to specifically examine the role of sediments as a source of iron to support Southern Ocean primary productivity. Total iron (Fe-T) in WAP sediments ranged from similar to 4 to 6 wt% Fe and showed no consistent depth variations. Total iron oxides (Fe-Ox) represented similar to 20-30% of Fe-T in WAP surface sediments and was comprised of two types of materials: Fe-ox1, which is thought to contain amorphous, highly reactive, and poorly crystalline iron oxides such as ferrihydrite and lepidocrocite, and Fe-ox2, which is thought to contain magnetite and less reactive, more crystalline iron oxides such as goethite and hematite. Absolute and relative concentrations of Fe-Ox declined with sediment depth, presumably due to reductive dissolution, and there was also a major depth change in the speciation of Fe-Ox. Near the sediment surface similar to 30% of Fe-Ox was Fe-ox1, while below similar to 30 cm Fe-ox1 was almost completely consumed and therefore here virtually all Fe-Ox was Fe-ox2. Consistent with these observations, a simple reaction-transport model applied to the depth distributions of Fe-ox1 and Fe-ox2 iron in WAP shelf sediments suggested a similar to 20-fold difference in the relative reactivity of these different oxides towards reductive dissolution (Fe-ox1 > Fe-ox2). At several stations profiles of pore water dissolved iron and solid phase Fe-ox1 can be explained by steady state iron redox cycling. In contrast, profiles at other stations showed evidence of non steady-state iron redox cycling. Seasonal changes in the sediment organic carbon rain rate at these sites may explain this latter behavior. Differences in the behavior of iron at different sites may be related to the interplay between changes in sediment redox conditions and their impact on bioturbation and iron redox cycling. Sediment iron sources to the water column include dissolved iron (similar to Fe2+) benthic fluxes as well as sediment resuspension processes that mix iron oxides (i.e., Fe-ox1) found in surface sediments into the bottom waters. The impact these benthic iron sources will have on surface water iron concentrations (and eventually primary production) will depend on transport processes that move this iron from deeper waters to surface waters. They will also depend on chemical transformations in the water column that affect iron bioavailability. While sediment processes (in general) appear to be an important source of iron to Southern Ocean surface waters, there is large uncertainty in their magnitude. However, the results presented here demonstrate that the suspended sediment flux of amorphous iron oxides needs to be considered when discussing sediment iron sources to Southern Ocean surface waters. (C) 2022 Elsevier Ltd. All rights reserved.
引用
收藏
页码:288 / 312
页数:25
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