Elizabeth C. Turner

Thick sulfate evaporite accumulations marking a mid-Neoproterozoic oxygenation event (Ten Stone Formation, Northwest Territories, Canada)

Thick sulfate evaporite accumulations are absent from Proterozoic strata between ca. 2000 and ca. 1000 Ma, and detailed sedimentologic, stratigraphic, and geochemical data for the oldest Neoproterozoic thick marine sulfate evaporite successions are largely lacking. The middle Neoproterozoic Ten Stone Formation (Little Dal Group, Northwest Territories, Canada) consists of ~500 m of pelagic lagoonal gypsite and anhydritite (rocks consisting of the minerals gypsum and anhydrite) deposited shortly before the ca. 811 Ma Bitter Springs carbon isotope anomaly in an intracratonic basin that developed prior to breakup of Rodinia. The thickness of regional stratigraphic subdivisions of this formation, defined by subtle silt- and carbonate-bearing intervals, indicates a minor terrigenous source in the southeast and a silled connection to the open ocean in the northwest. Deposition of the Ten Stone Formation began with abrupt, tectonically triggered subsidence and restriction, and ended equally abruptly, as shown by stratigraphic contacts across which lithofacies corresponding to strikingly different paleoenvironments change sharply, with no evidence for hiatus or erosion. Stratigraphic cyclicity in the evaporite succession is minimal owing to isolation of bottom-hugging, dense lagoonal brine from overlying waters. Deposition of the Ten Stone Formation in a basin that experienced intermittent, basin-scale tectonic adjustments, as recorded by details of its stratigraphy, supports the interpretation that the Mackenzie Mountains Supergroup accumulated in an extensional, tectonically active intracratonic basin whose structure resembled a lower-plate extensional system. The absence of halite from the Ten Stone Formation contrasts with its abundance in the stratigraphically lower, gypsum-free Dodo Creek Formation, suggesting that deposition of the lower to middle Little Dal Group spanned a major oxygenation event, during which the sequence of evaporite mineral precipitation from seawater changed from halite-first to sulfate-first in response to rapid accumulation of atmospheric oxygen and concomitant increase in the global marine sulfate reservoir. The limited range of sulfur isotope values in a new data set spanning hundreds of meters of gypsite indicates a strongly and persistently oxidizing mid-Neoproterozoic atmosphere, an abundance of sulfate in seawater, and marine oxygenation extending below storm wave base. The mineralogy, sedimentology, stratigraphy, and geochemistry of the Ten Stone Formation are virtually indistinguishable from those of thick, Phanerozoic “deep-water” (below wave-base) evaporite successions, and indicate that the tectonic, climatic, and geochemical conditions required for deposition of thick successions of marine sulfate evaporites were well established prior to ca. 811 Ma. Thick sulfate evaporite successions in equivalent stratigraphic positions just below the Bitter Springs carbon isotope excursion elsewhere in Laurentia, as well as on the Congo craton, and in South Australia attest to the global impact of the rapidly increased seawater sulfate reservoir prior to Rodinia’s breakup. High relative burial rates of organic matter prevailed before the breakup of Rodinia and led to oxygenation of the atmosphere-ocean system, growth of the seawater sulfate reservoir, and, in association with a warm and arid climate, deposition for the first time in Earth’s history of thick sulfate evaporites in the middle Neoproterozoic, ~100 m.y. before the first Cryogenian glacial episode. The Neoproterozoic Oxygenation Event may have taken place in several steps, the first of which preceded the Bitter Springs anomaly.

Mesoproterozoic carbonate systems in the Borden Basin, Nunavut

Existing stratigraphic nomenclature, lithologic descriptions, and geological interpretations for an economically important Mesoproterozoic dolostone in the Milne Inlet Graben, Borden Basin, Nunavut, do not adequately portray its unusual facies or their spatio-temporal configuration. Four new stratigraphic units are introduced to replace this dolostone, formerly known as the Society Cliffs Formation. In the southeastern half of the graben, the Iqqittuq Formation represents a distally steepened ramp that grades northwestward into deep-water mudstone that is indistinguishable from that of the underlying Arctic Bay Formation. The overlying Angmaat Formation represents a rimmed, restricted peritidal platform that grades northwestward across a tepee – cortoid shoal barrier into the unusual, deep-water dolo-laminite of the Nanisivik Formation. Deep-water carbonate mounds up to hundreds of metres thick and kilometres in areal dimensions belong to the Ikpiarjuk Formation; these mounds are geometrically equivalent ...

In situ trace metal analysis of Neoarchaean – Ordovician shallow‐marine microbial‐carbonate‐hosted pyrites

Pre-Cambrian atmospheric and oceanic redox evolutions are expressed in the inventory of redox-sensitive trace metals in marine sedimentary rocks. Most of the currently available information was derived from deep-water sedimentary rocks (black shale/banded iron formation). Many of the studied trace metals (e.g. Mo, U, Ni and Co) are sensitive to the composition of the exposed land surface and prevailing weathering style, and their oceanic inventory ultimately depends on the terrestrial flux. The validity of claims for increased/decreased terrestrial fluxes has remained untested as far as the shallow-marine environment is concerned. Here, the first systematic study of trace metal inventories of the shallow-marine environment by analysis of microbial carbonate-hosted pyrite, from ca. 2.65-0.52 Ga, is presented. A petrographic survey revealed a first-order difference in preservation of early diagenetic pyrite. Microbial carbonates formed before the 2.4 Ga great oxygenation event (GOE) are much richer in pyrite and contain pyrite grains of greater morphological variability but lesser chemical substitution than samples deposited after the GOE. This disparity in pyrite abundance and morphology is mirrored by the qualitative degree of preservation of organic matter (largely as kerogen). Thus, it seems that in microbial carbonates, pyrite formation and preservation were related to presence and preservation of organic C. Several redox-sensitive trace metals show interpretable temporal trends supporting earlier proposals derived from deep-water sedimentary rocks. Most notably, the shallow-water pyrite confirms a rise in the oceanic Mo inventory across the pre-Cambrian-Cambrian boundary, implying the establishment of efficient deep-ocean ventilation. The carbonate-hosted pyrite also confirms the Neoarchaean and early Palaeoproterozoic ocean had higher Ni concentration, which can now more firmly be attributed to a greater proportion of magnesian volcanic rock on land rather than a stronger hydrothermal flux of Ni. Additionally, systematic trends are reported for Co, As, and Zn, relating to terrestrial flux and oceanic productivity.

Implications of selective predation on the macroevolution of eukaryotes: evidence from Arctic Canada

Existing paleontological data indicate marked eukaryote diversification in the Neoproterozoic, ca. 800 Ma, driven by predation pressure and various other biotic and abiotic factors. Although the eukaryotic record remains less diverse before that time, molecular clock estimates and earliest crown-group affiliated microfossils suggest that the diversification may have originated during the Mesoproterozoic. Within new assemblages of organic-walled microfossils from the ca. 1150 to 900 Ma lower Shaler Supergroup of Arctic Canada, numerous specimens from various taxa display circular and ovoid perforations on their walls, interpreted as probable traces of selective protist predation, 150-400 million years before their first reported incidence in the Neoproterozoic. Selective predation is a more complex behavior than phagotrophy, because it requires sensing and selection of prey followed by controlled lysis of the prey wall. The ca. 800 Ma eukaryotic diversification may have been more gradual than previously thought, beginning in the late Mesoproterozoic, as indicated by recently described microfossil assemblages, in parallel with the evolution of selective eukaryovory and the spreading of eukaryotic photosynthesis in marine environments.