Diagenesis in tephra-rich sediments from the Lesser Antilles Volcanic Arc: Pore fluid constraints

被引:22
|
作者
Murray, Natalie A. [1 ]
McManus, James [1 ,2 ,3 ]
Palmer, Martin R. [4 ]
Haley, Brian [3 ]
Manners, Hayley [4 ,5 ]
机构
[1] Univ Akron, Dept Geosci, Akron, OH 44325 USA
[2] Bigelow Lab Ocean Sci, 60 Bigelow Dr, East Boothbay, ME 04544 USA
[3] Oregon State Univ, Coll Earth Ocean & Atmospher Sci, Corvallis, OR 97331 USA
[4] Univ Southampton, Natl Oceanog Ctr Southampton, Sch Ocean & Earth Sci, Southampton SO14 3ZH, Hants, England
[5] Univ Plymouth, Sch Geog Earth & Environm Sci, Plymouth PL4 8AA, Devon, England
基金
美国国家科学基金会;
关键词
DEEP-SEA SEDIMENTS; FLANK-COLLAPSE EVENTS; IODP SITE U1396; INTERSTITIAL WATERS; GEOCHEMICAL CYCLES; NANKAI TROUGH; SR-ISOTOPES; TEMPERATURE; CARBONATES; MIGRATION;
D O I
10.1016/j.gca.2018.02.039
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 present sediment pore fluid and sediment solid phase results obtained during IODP Expedition 340 from seven sites located within the Grenada Basin of the southern Lesser Antilles Volcanic Arc region. These sites are generally characterized as being low in organic carbon content and rich in calcium carbonate and volcanogenic material. In addition to the typical reactions related to organic matter diagenesis, pore fluid chemistry indicates that the diagenetic reactions fall within two broad categories; (1) reactions related to chemical exchange with volcanogenic material and (2) reactions related to carbonate dissolution, precipitation, or recrystallization. For locations dominated by reaction with volcanogenic material, these sites exhibit increases in dissolved Ca with coeval decreases in Mg. We interpret this behavior as being driven by sediment-water exchange reactions from the alteration of volcanic material that is dispersed throughout the sediment package, which likely result in formation of Mg-rich secondary authigenic clays. In contrast to this behavior, sediment sequences that exhibit decreases in Ca, Mg, Mn, and Sr with depth suggest that carbonate precipitation is an active diagenetic process affecting solute distributions. The distributions of pore fluid Sr-87/Sr-86 reflect these competitive diagenetic reactions between volcanic material and carbonate, which are inferred by the major cation distributions. From one site where we have solid phase Sr-87/Sr-86 (site U1396), the carbonate fraction is found to be generally consistent with the contemporaneous seawater isotope values. However, the Sr-87/Sr-86 of the non-carbonate fraction ranges from 0.7074 to 0.7052, and these values likely represent a mixture of local arc volcanic sources and trans-Atlantic eolian sources. Even at this site where there is clear evidence for diagenesis of volcanogenic material, carbonate diagenesis appears to buffer pore fluid Sr-87/Sr-86 from the larger changes that might be expected given the high abundance of tephra in these sediments. Part of this carbonate buffering, at this site as well as throughout the region, derives from the fact that the Sr concentration in the non-carbonate fraction is generally low (<200 ppm), whereas the carbonate fraction has Sr concentrations approaching similar to 1000 ppm. (C) 2018 Elsevier Ltd. All rights reserved.
引用
收藏
页码:119 / 135
页数:17
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