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Ferruginous conditions dominated later neoproterozoic deep-water chemistry
被引:656
作者:
Canfield, Donald E.
[1
,2
]
Poulton, Simon W.
[3
]
Knoll, Andrew H.
[4
]
Narbonne, Guy M.
[5
]
Ross, Gerry
[6
]
Goldberg, Tatiana
[3
]
Strauss, Harald
[7
]
机构:
[1] Univ So Denmark, Nord Ctr Earth Evolut, DK-5230 Odense, Denmark
[2] Univ So Denmark, Inst Biol, DK-5230 Odense, Denmark
[3] Newcastle Univ, Sch Civil Engn & Geosci, Newcastle Upon Tyne NE1 7RU, Tyne & Wear, England
[4] Harvard Univ, Bot Museum, Cambridge, MA 02138 USA
[5] Queens Univ, Dept Geol Sci & Geol Engn, Kingston, ON K7L 3N6, Canada
[6] Kupaa Farm, Kula, HI 96790 USA
[7] Univ Munster, Inst Geol Palaontol, D-48149 Munster, Germany
来源:
基金:
英国自然环境研究理事会;
关键词:
D O I:
10.1126/science.1154499
中图分类号:
O [数理科学和化学];
P [天文学、地球科学];
Q [生物科学];
N [自然科学总论];
学科分类号:
07 ;
0710 ;
09 ;
摘要:
Earth's surface chemical environment has evolved from an early anoxic condition to the oxic state we have today. Transitional between an earlier Proterozoic world with widespread deep- water anoxia and a Phanerozoic world with large oxygen- utilizing animals, the Neoproterozoic Era [ 1000 to 542 million years ago ( Ma)] plays a key role in this history. The details of Neoproterozoic Earth surface oxygenation, however, remain unclear. We report that through much of the later Neoproterozoic (< 742 +/- 6 Ma), anoxia remained widespread beneath the mixed layer of the oceans; deeper water masses were sometimes sulfidic but were mainly Fe2+- enriched. These ferruginous conditions marked a return to ocean chemistry not seen for more than one billion years of Earth history.
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页码:949 / 952
页数:4
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