Person:

Sperling, Erik A.

A mechanistic understanding of relationships between global glaciation, a putative second rise in atmospheric oxygen, the Shuram carbon isotope excursion, and the appearance of Ediacaran-type fossil impressions and bioturbation is dependent on the construction of accurate geological records through regional stratigraphic correlations. Here we integrate chemo-, litho-, and sequence-stratigraphy of fossiliferous Ediacaran strata in northwestern Canada. These data demonstrate that the FAD of Ediacara-type fossil impressions in northwestern Canada occur within a lowstand systems tract and above a major sequence boundary in the informally named June beds, not in the early Ediacaran Sheepbed Formation from which they were previously reported. This distinction is substantiated by δ13Ccarb chemostratigraphy of the Sheepbed carbonate, which overlies the Sheepbed Formation, and the Gametrail Formation, which overlies the June beds. The Sheepbed carbonate hosts heavy δ13Ccarb values whereas the Gametrail Formation contains a large δ13Ccarb excursion, which we correlate with the globally recognized Shuram excursion. Stratigraphically above the Gametrail excursion, the first bilaterian burrows are present in the basal Blueflower Formation. Together, these data allow us to construct an age model for Ediacaran strata in northwestern Canada and conclude that a purported shift in Fe speciation in the Sheepbed Formation significantly predates the shift recorded above the ca. 582 Ma Gaskiers glaciation in Newfoundland and the first appearance of Ediacaran biota. The Gametrail excursion shares many characteristics with Shuram negative δ13Ccarb excursion: 1) δ13Ccarb and δ18Ocarb covary; 2) δ13Ccarb and δ13Corg do not covary; 3) the excursion is developed during a transgressive systems tract and recovers in an highstand systems tract; and 4) values in some sections are well below mantle δ13C input values but are variable between sections. We relate regional lateral variability in the magnitude and character of this excursion to condensation and diachronous deposition during the transgression and local authigenic carbonate production. In light of these observations, we explore a variety of models for the genesis of the Shuram excursion and suggest that the location and amount of authigenic carbonate production played a role in the excursion.

Geological mapping and stratigraphic anaylsis of the early Neoproterozoic Fifteenmile Group in the western Ogilvie Mountains of Yukon, Canada, has revealed large lateral facies changes in both carbonate and siliciclastic strata. Syn-sedimentary NNW-side-down normal faulting during deposition of the lower Fifteenmile Group generated local topographic relief and wedge-shaped stratal geometries. These strata were eventually capped by platformal carbonate after the establishment of a NNW-facing stromatolitic reef complex that formed adjacent to the coeval Little Dal Group of the Mackenzie Mountains, Northwest Territories. Correlations between specific formations within these groups are tested with carbon isotope chemostratigraphy. As there are no known 830-780 Ma stratigraphic successions south of 62°N, the basin-forming event that accommodated the Fifteenmile and Little Dal Groups of the Ogilvie and Mackenzie Mountains and equivalent strata in the Shaler Supergroup of Victoria Island was restricted to the northwest margin of Laurentia. Therefore, this event does not represent widespread rifting of the entire western margin of Laurentia and instead we propose that these strata were accommodated in a failed rift generated by localized subsidence associated with the emplacement of the coeval Guibei (China) and Gairdner (Australia) large igneous provinces. The northern margin of Laurentia was reactivated by renewed extension at ca. 720 Ma associated with the emplacement of the Franklin large igneous province. Significant crustal thinning and generation of a thermally subsiding passive margin on the western margin of Laurentia may not have occurred until the late Ediacaran.

Living animals display a variety of morphological, physiological, and biochemical characters that enable them to live in low-oxygen environments. These features and the organisms that have evolved them are distributed in a regular pattern across dioxygen (O2) gradients associated with modern oxygen minimum zones. This distribution provides a template for interpreting the stratigraphic covariance between inferred Ediacaran-Cambrian oxygenation and early animal diversification. Although Cambrian oxygen must have reached 10--20% of modern levels, sufficient to support the animal diversity recorded by fossils, it may not have been much higher than this. Today’s levels may have been approached only later in the Paleozoic Era. Nonetheless, Ediacaran-Cambrian oxygenation may have pushed surface environments across the low, but critical, physiological thresholds required for large, active animals, especially carnivores. Continued focus on the quantification of the partial pressure of oxygen (pO2) in the Proterozoic will provide the definitive tests of oxygen-based coevolutionary hypotheses.

The ca. 2.45–2.22 Ga Turee Creek Group, Western Australia, contains carbonate- rich horizons that postdate earliest Proterozoic iron formations, bracket both Paleoproterozoic glaciogenic beds and the onset of the Great Oxidation Event (GOE), and predate ca. 2.2–2.05 Ga Lomagundi-Jatuli C-isotopic excursion(s). As such, Turee Creek carbonate strata provide an opportunity to characterize early Paleoproterozoic carbonate sedimentation and carbon cycle dynamics in the context of significant global change. Here, we report on the stratigraphy, sedimentology, petrology, carbon isotope chemostratigraphy, and stromatolite development for carbonate-rich successions within the pre-glacial part of the Kungarra Formation and the postglacial Kazput Formation. Kungarra carbonate units largely occur as laterally discontinuous beds within a thick, predominantly siliciclastic shelf deposit. While this succession contains thin microbialite horizons, most carbonates consist of patchy calcite overgrowths within a siliciclastic matrix. C-isotopic values show marked variation along a single horizon and even within hand samples, reflecting spatially and temporally variable mixing between dissolved inorganic carbon in seawater and isotopically light inorganic carbon generated via syn- and post-depositional remineralization of organic matter. In contrast, the Kazput carbonates consist of subtidal stromatolites, grainstones, and micrites deposited on a mixed carbonate-siliciclastic shelf. These carbonates exhibit moderate δ13 C values of -2‰ to +1.5‰ and likely preserve a C-isotopic signature of seawater. Kazput carbonates, thus, provide some of the best available evidence that an interval of unexceptional C-isotopic values separates the Lomagundi-Jatuli C-isotopic excursion(s) from the initiation of the GOE as inferred from multiple sulfur isotopes (loss 4 of mass independent fractionation). The Kazput Formation also contains unusual, m-scale stromatolitic buildups, which are composed of sub-mm laminae and discontinuous, convex upward lenticular precipitates up to a few mm in maximum thickness. Laminae, interpreted as microbial mat layers, contain quartz and clay minerals as well as calcite, whereas precipitate lenses consist of interlocking calcite anhedra, sometimes showing faint mm-scale banding. These cements formed either as infillings of primary voids formed by gas emission within penecontemporaneously lithified mats, or as local seafloor precipitates that formed on, or within, surface mats. It is possible that both mechanisms interacted to form the unique Kazput stromatolites. These microbialites speak to a distinctive interaction between life and environment early in the Paleoproterozoic Era.

Multiple eukaryotic clades make their first appearance in the fossil record between ~810 and 715 Ma. Molecular clock studies suggest that the origin of animal multicellularity may have been part of this broader eukaryotic radiation. Animals require oxygen to fuel their metabolism, and low oxygen levels have been hypothesized to account for the temporal lag between metazoan origins and the Cambrian radiation of large, ecologically diverse animals. Here, paleoredox conditions were investigated in the Fifteenmile Group, Ogilvie Mountains, Yukon, Canada, which hosts an 811 Ma ash horizon and spans the temporal window that captures the inferred origin and early evolution of animals. Iron-based redox proxies, redox-sensitive trace elements, organic carbon percentages and pyrite sulfur isotopes were analyzed in seven stratigraphic sections along two parallel basin transects. These data suggest that for this basin, oxygenated shelf waters overlay generally anoxic deeper waters. The anoxic water column was dominantly ferruginous, but brief periods of euxinia likely occurred. These oscillations coincide with changes in total organic carbon, suggesting euxinia was primarily driven by increased organic carbon loading. Overall, these data are consistent with proposed quantitative constraints on Proterozoic atmospheric oxygen being greater than 1% of modern levels, but less than present levels. Comparing these oxygen levels against the likely oxygen requirements of the earliest animals, both theoretical considerations and the ecology of modern oxygen-deficient settings suggest that the inferred oxygen levels in the mixed layer would not have been prohibitive to the presence of sponges, eumetazoans or bilaterians. Thus the evolution of the earliest animals was probably not limited by the low absolute oxygen levels that may have characterized Neoproterozoic oceans, although these inferred levels would constrain animals to very small sizes and low metabolic rates.

The Proterozoic-Cambrian transition records the appearance of essentially all animal body plans (phyla), yet to date no single hypothesis adequately explains both the timing of the event and the evident increase in diversity and disparity. Ecological triggers focused on escalatory predator–prey “arms races” can explain the evolutionary pattern but not its timing, whereas environmental triggers, particularly ocean/atmosphere oxygenation, do the reverse. Using modern oxygen minimum zones as an analog for Proterozoic oceans, we explore the effect of low oxygen levels on the feeding ecology of polychaetes, the dominant macrofaunal animals in deep-sea sediments. Here we show that low oxygen is clearly linked to low proportions of carnivores in a community and low diversity of carnivorous taxa, whereas higher oxygen levels support more complex food webs. The recognition of a physiological control on carnivory therefore links environmental triggers and ecological drivers, providing an integrated explanation for both the pattern and timing of Cambrian animal radiation.

A substantial body of evidence suggests that subsurface water masses in mid-Proterozoic marine basins were commonly anoxic, either euxinic (sulfidic) or ferruginous (free ferrous iron). To further document redox variations during this interval, a multiproxy geochemical and paleobiological investigation was conducted on the approximately 1000-m-thick Mesoproterozoic (Lower Riphean) Arlan Member of the Kaltasy Formation, central Russia. Iron speciation geochemistry, supported by organic geochemistry, redox-sensitive trace element abundances, and pyrite sulfur isotope values, indicates that basinal calcareous shales of the Arlan Member were deposited beneath an oxygenated water column, and consistent with this interpretation, eukaryotic microfossils are abundant in basinal facies. The Rhenium–Osmium (Re–Os) systematics of the Arlan shales yield depositional ages of 1414 ± 40 and 1427 ± 43 Ma for two horizons near the base of the succession, consistent with previously proposed correlations. The presence of free oxygen in a basinal environment adds an important end member to Proterozoic redox heterogeneity, requiring an explanation in light of previous data from time-equivalent basins. Very low total organic carbon contents in the Arlan Member are perhaps the key—oxic deep waters are more likely (under any level of atmospheric O2) in oligotrophic systems with low export production. Documentation of a full range of redox heterogeneity in subsurface waters and the existence of local redox controls indicate that no single stratigraphic section or basin can adequately capture both the mean redox profile of Proterozoic oceans and its variance at any given point in time.

Sedimentary rocks deposited across the Proterozoic–Phanerozoic transition record extreme climate fluctuations, a potential rise in atmospheric oxygen or re-organization of the seafloor redox landscape, and the initial diversification of animals. It is widely assumed that the inferred redox change facilitated the observed trends in biodiversity. Establishing this palaeoenvironmental context, however, requires that changes in marine redox structure be tracked by means of geochemical proxies and translated into estimates of atmospheric oxygen. Iron-based proxies are among the most effective tools for tracking the redox chemistry of ancient oceans. These proxies are inherently local, but have global implications when analysed collectively and statistically. Here we analyse about 4,700 iron-speciation measurements from shales 2,300 to 360 million years old. Our statistical analyses suggest that subsurface water masses in mid-Proterozoic oceans were predominantly anoxic and ferruginous (depleted in dissolved oxygen and iron-bearing), but with a tendency towards euxinia (sulfide-bearing) that is not observed in the Neoproterozoic era. Analyses further indicate that early animals did not experience appreciable benthic sulfide stress. Finally, unlike proxies based on redox-sensitive trace-metal abundances, iron geochemical data do not show a statistically significant change in oxygen content through the Ediacaran and Cambrian periods, sharply constraining the magnitude of the end-Proterozoic oxygen increase. Indeed, this re-analysis of trace-metal data is consistent with oxygenation continuing well into the Palaeozoic era. Therefore, if changing redox conditions facilitated animal diversification, it did so through a limited rise in oxygen past critical functional and ecological thresholds, as is seen in modern oxygen minimum zone benthic animal communities.

The causes behind the appearance of abundant macroscopic body and trace fossils at the end of the Neoproterozoic Era remain debated. Iron geochemical data from fossiliferous Ediacaran successions in Newfoundland suggested that the first appearances correlated with an oxygenation event. A similar relationship was claimed to exist in the Mackenzie Mountains, Canada, although later stratigraphic studies indicated that the sections analyzed for geochemistry were incorrectly correlated with those hosting the fossils. To directly connect fossil occurrences with geochemistry in the Mackenzie Mountains, we conducted a multiproxy iron, carbon, sulfur, and trace-element geochemical analysis of stratigraphic sections hosting both the Cryogenian “Twitya discs” at Bluefish Creek as well as Ediacaran fossils and simple bilaterian traces at Sekwi Brook. There is no clear oxygenation event correlated with the appearance of macroscopic body fossils or simple bilaterian burrows; however, some change in environment—a potential partial oxygenation—is correlated with increasing burrow width higher in the Blueflower Formation. Data from Sekwi Brook suggest that these organisms were periodically colonizing a predominantly anoxic and ferruginous basin. This seemingly incongruent observation is accommodated through accounting for differing time scales between the characteristic response time of sedimentary redox proxies versus that for ecological change. Thus, hypotheses directly connecting ocean oxygenation with the appearance of macrofossils need not apply to all areas of a heterogeneous Ediacaran ocean, and stably oxygenated conditions on geological time scales were not required for the appearance of these Avalon-assemblage Ediacaran organisms. At least in the Mackenzie Mountains, the appropriate facies for fossil preservation appears to be the strongest control on the stratigraphic distribution of macrofossils.