Abstract

We report Si-isotopic compositions of 75 sedimentologically and petrographically characterized chert samples with ages ranging from ∼2600 to 750Ma using multi-collector inductively coupled plasma mass spectrometry. δ30Si values of the cherts analyzed in this study show a ∼7‰ range, from −4.29 to +2.85. This variability can be explained in part by (1) simple mixing of silica derived from continental (higher δ30Si) and hydrothermal (lower δ30Si) sources, (2) multiple mechanisms of silica precipitation and (3) Rayleigh-type fractionations within pore waters of individual basins.We observe ∼3‰ variation in peritidal cherts from a single Neoproterozoic sedimentary basin (Spitsbergen). This variation can be explained by Rayleigh-type fractionation during precipitation from silica-saturated porewaters. In some samples, post-dissolution and reprecipitation of silica could have added to this effect. Our data also indicate that peritidal cherts are enriched in the heavier isotopes of Si whereas basinal cherts associated with banded iron formations (BIF) show lower δ30Si. This difference could partly be due to Si being derived from hydrothermal sources in BIFs. We postulate that the difference in δ30Si between non-BIF and BIF cherts is consistent with the contrasting genesis of these deposits. Low δ30Si in BIF is consistent with laboratory experiments showing that silica adsorbed onto Fe-hydroxide particles preferentially incorporates lighter Si isotopes.Despite large intrabasinal variation and environmental differences, the data show a clear pattern of secular variation. Low δ30Si in Archean cherts is consistent with a dominantly hydrothermal source of silica to the oceans at that time. The monotonically increasing δ30Si from 3.8 to 1.5Ga appears to reflect a general increase in continental versus hydrothermal sources of Si in seawater, as well as the preferential removal of lighter Si isotopes during silica precipitation in iron-associated cherts from silica-saturated seawater. The highest δ30Si values are observed in 1.5Ga peritidal cherts; in part, these enriched values could reflect increasing sequestration of light silica during soil-forming processes, thus, delivering relatively heavy dissolved silica to the oceans from continental sources. The causes behind the reversal in trend towards lower δ30Si in cherts younger than 1.5Ga old are less clear. Cherts deposited 1800–1900Ma are especially low δ30Si, a possible indication of transiently strong hydrothermal input at this time.

Highlights

  • Cherts, deposits of amorphous silica microcrystalline quartz, are ubiquitous in the sedimentary rock record, documenting the evolution of the global silica cycle through geologic time (Maliva et al, 1989, 2005)

  • We have presented the first high-precision MC-ICPMS measurements of the Si isotopic composition of Proterozoic cherts

  • In combination with other available MC-ICPMS measurements of Precambrian cherts, our data indicate that peritidal cherts, formed by early diagenetic replacement of carbonates, show relatively high d30Si compared to basinal cherts associated with banded iron formations (BIF)

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Summary

Introduction

Deposits of amorphous silica microcrystalline quartz, are ubiquitous in the sedimentary rock record, documenting the evolution of the global silica cycle through geologic time (Maliva et al, 1989, 2005). The isotopic composition of Si in Archean and Proterozoic cherts can provide insights into the sources and sinks of marine silica before the evolution of silica-precipitating sponges, radiolarians and diatoms. The use of sedimentary silica as a direct proxy for the composition and physical state of Precambrian seawater has limitations because most Precambrian cherts formed during the diagenesis of precursor sediments. Robert and Chaussidon (2006) measured the Si isotopic composition of an extensive set of chert samples, primarily from Archean and Proterozoic successions, and including Phanerozoic examples, using an ion-microprobe technique. They interpreted their combined O and Si isotope data from Precambrian cherts to reflect seawater paleo-temperatures. Subsequent studies have highlighted the importance of the source of Si in determining the isotopic composition of preserved cherts (van den Boorn et al, 2007, 2010; Steinhoefel et al, 2009; Heck et al, 2011)

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