학술논문

Siderite concretions from nonmarine shales (Westphalian A) of the Pennines, England; controls on their growth and composition
Document Type
Academic Journal
Source
Journal of Sedimentary Research. 68(5):1034-1045
Subject
06A|Sedimentary petrology - sed rocks, sediments
carbonates
Carboniferous
clastic rocks
composition
concretions
controls
depositional environment
England
Europe
Great Britain
Paleozoic
Pennines
secondary structures
sedimentary rocks
sedimentary structures
shale
siderite
terrestrial environment
United Kingdom
Upper Carboniferous
Western Europe
Westphalian
Language
English
ISSN
1527-1404
Abstract
Back-scattered electron microscopy has been used to examine the microstructure of nonmarine-shale-hosted siderite concretions. The concretions are composed of 50-100 micrometer, zoned crystallites, which exhibit no noticeable center-to-edge variation within any individual concretion. This indicates that siderite crystallites nucleated at virtually the same time across the entire concretion and that the concretions did not grow by radial addition of siderite layers around a central nucleus. Further siderite precipitation took place by crystal growth onto the nuclei. The total proportion of siderite in any part of the concretion bears no simple relationship to the porosity of the enclosing shale at the time of precipitation, and growth by passive precipitation in pore space is unlikely. Integration of microprobe data with bulk mineral-chemical and stable-isotope data suggests that the siderite crystallites are composed of an Fe-Mn-rich end member with a δ13C value of ∼ +10 per mil and a Mg-Ca-rich end member with a δ13 C value of ∼ 0 per mil to -5 per mil. The mineral-chemical and stable-isotope compositions of these concretions resulted from microbially mediated processes operating close (13C as well as high-δ13 C carbonate cements, hence deep-burial diagenetic reactions, such as decarboxylation of organic matter, need not be invoked to generate solutes for siderite precipitation.