Organogenic dolomitization in peritidal to deep-sea sediments

TitleOrganogenic dolomitization in peritidal to deep-sea sediments
Publication TypeJournal Article
Year of Publication2000
AuthorsMazzullo, SJ
JournalJournal of Sedimentary Research
Volume70
Issue1
Pagination10-23
Date PublishedJan
ISSN1073-130x
Accession NumberWOS:000085513100002
Abstract

Presumed barriers to early dolomitization in normal seawater-derived pore fluids at earth-surface temperatures appear to be overcome within some anoxic, organic-rich sediments as a result of bacterial sulfate reduction and methanogenesis, These processes may promote early dolomitization, particularly during methanogenesis and late stages of sulfate reduction, by concurrently raising and sustaining high pH and high total alkalinity and CO32- concentrations in pore fluids, and by simultaneously either decreasing Mg and Ca hydration or by promoting crystal surface reactions with less hydrated Mg-Ca neutral ion pairs. Volumetrically significant quantities of dolomite are associated with sulfate reduction and/or methanogenesis within peritidal, shallow-marine, and deep-sea deposits. Average concentrations of organogenic dolomite are as much as 70% in some Holocene peritidal deposits, and 28% in Mesozoic to Quaternary deep-sea sediments.Organogenic dolomites are mainly cements, and contain relatively low concentrations of Sr and Mn, Sulfate-reduction dolomites generally are Fe-deficient because of concurrent pyrite precipitation, whereas methanogenetic dolomites may be somewhat more ferroan as Fe substitutes for depleting Mg. Sources of Mg and Ca for dolomite are diffusion from overlying seawater and/or dissolution of precursor carbonate sediments. Dolomites are characterized by a wide range in delta(13)C values wherein those of sulfate reduction versus methanogenetic origin typically are C-13-depleted and C-13-enriched, respectively. The extent of C-13 depletion or enrichment, however, depends on the extent of organodiagenetic reactions and amount of C-13 contributed by seawater diffusion, and commonly results in overlap of delta(13)C(dolomite) values. The range of delta(18)O(dolomite) values is somewhat more restricted, and generally reflects differences in pore-fluid temperature and salinity. Some of the unresolved issues in organogenic dolomitization are: the relative efficiencies of sulfate reduction versus methanogenesis in promoting dolomitization, depths of dolomite formation inferred on the basis of delta(18)O(dolomite) values and probable sources of Mg and Ca, and the mode of dolomitization with progressive burial into methanogenetic zones.

DOI10.1306/2dc408f9-0e47-11d7-8643000102c1865d