A c c e p t e d M a n u s c r i p t 3 ABSTRACTThe first appearance of skeletal metazoans in the late Ediacaran (~550 million years ago; Ma) has been linked to the widespread development of oxygenated oceanic conditions, but a precise spatial and temporal reconstruction of their evolution has not been resolved. Here we consider the evolution of ocean chemistry from ~550 to ~541 Ma across shelf-to-basin transects in the Zaris and Witputs Sub-Basins of the Nama Group, Namibia. New carbon isotope data capture the final stages of the Shuram/Wonoka deep negative C-isotope excursion, and these are complemented with a reconstruction of water column redox dynamics utilizing Fe-S-C systematics and the distribution of skeletal and soft-bodied metazoans. Combined, these inter-basinal datasets provide insight into the potential role of ocean redox chemistry during this pivotal interval of major biological innovation.The strongly negative 13 C values in the lower parts of the sections reflect both a secular, global change in the C-isotopic composition of Ediacaran seawater, as well as the influence of 'local' basinal effects as shown by the most negative 13 C values occurring in the transition from distal to proximal ramp settings. Critical, though, is that the transition to positive 13 C values postdates the appearance of calcified metazoans, indicating that the onset of biomineralization did not occur under post-excursion conditions. Significantly, we find that anoxic and ferruginous deeper water column conditions were prevalent during and after the transition to positive 13 C that marks the end of the Shuram/Wonoka excursion. Thus, if the C isotope trend reflects the transition to global-scale oxygenation in the aftermath of the oxidation of a large-scale, isotopically light organic carbon pool, it was not sufficient to fully oxygenate the deep ocean. Page 4 of 74A c c e p t e d M a n u s c r i p t 4 Both sub-basins reveal highly dynamic redox structures, where shallow, inner ramp settings experienced transient oxygenation. Anoxic conditions were caused either by episodic upwelling of deeper anoxic waters or higher rates of productivity. These settings supported short-lived and monospecific skeletal metazoan communities. By contrast, microbial (thrombolite) reefs, found in deeper inner-and mid-ramp settings, supported more biodiverse communities with complex ecologies and large skeletal metazoans. These long-lived reef communities, as well as Ediacaran soft-bodied biotas, are found particularly within transgressive systems, where oxygenation was persistent. We suggest that a mid-ramp position enabled physical ventilation mechanisms for shallow water column oxygenation to operate during flooding and transgressive sea-level rise. Our data support a prominent role for oxygen, and for stable oxygenated conditions in particular, in controlling both the distribution and ecology of Ediacaran skeletal metazoan communities.Keywords: Oxygenation; Neoproterozoic; Biomineralisation; Metazoans; Ediacaran; Ecosystems Introductio...
The 'Cambrian Explosion' describes the rapid increase in animal diversity and abundance, as manifest in the fossil record, between ~ 540 and 520 million years ago (Ma). This event, however, is nested within a far more ancient record of macrofossils extending at least into the late Ediacaran, ~571 Ma. The evolutionary events documented during the Ediacaran-Cambrian interval coincide with geochemical evidence for the modernisation of Earth's biogeochemical cycles. Holistic integration of fossil and geochemical records leads us to challenge the notion that the Ediacaran and Cambrian worlds were markedly distinct, and places biotic and environmental change within a longer-term narrative. We propose that the evolution of metazoans may have been facilitated by a series of dynamic and global changes in redox conditions and nutrient supply, which, together with potential biotic feedbacks, enabled turnover events that sustained phases of radiation. In this synthesis, we argue that early metazoan diversification should be recast as a series of successive, transitional radiations that extended from the late Ediacaran and continued through the early Palaeozoic. We conclude that while the Cambrian Explosion represents a radiation of crown-group bilaterians, it was simply one phase amongst several older, and younger, metazoan radiations.
The oceans at the start of the Neoproterozoic Era (1,000–541 million years ago, Ma) were dominantly anoxic, but may have become progressively oxygenated, coincident with the rise of animal life. However, the control that oxygen exerted on the development of early animal ecosystems remains unclear, as previous research has focussed on the identification of fully anoxic or oxic conditions, rather than intermediate redox levels. Here we report anomalous cerium enrichments preserved in carbonate rocks across bathymetric basin transects from nine localities of the Nama Group, Namibia (∼550–541 Ma). In combination with Fe-based redox proxies, these data suggest that low-oxygen conditions occurred in a narrow zone between well-oxygenated surface waters and fully anoxic deep waters. Although abundant in well-oxygenated environments, early skeletal animals did not occupy oxygen impoverished regions of the shelf, demonstrating that oxygen availability (probably >10 μM) was a key requirement for the development of early animal-based ecosystems.
Reef-building in metazoans represents an important ecological innovation whereby individuals collectively enhance feeding efficiency and gain protection from competitors and predation. The appearance of metazoan reefs in the fossil record therefore indicates an adaptive response to complex ecological pressures. In the Nama Group, Namibia, we found evidence of reef-building by the earliest known skeletal metazoan, the globally distributed Cloudina, ~548 million years ago. These Cloudina reefs formed open frameworks without a microbial component but with mutual attachment and cementation between individuals. Orientated growth implies a passive suspension-feeding habit into nutrient-rich currents. The characteristics of Cloudina support the view that metazoan reef-building was promoted by the rise of substrate competitors and predators.
Anoxic and iron-rich oceanic conditions prevailed throughout most of the Archean and Proterozoic (4000 to c.540 million years ago, Ma), but the oceans are hypothesised to have become progressively oxygen-rich during the Ediacaran-Cambrian transition interval, coincident with the rise of animal life. We utilise the uranium isotope ratio of seawater (238 U/ 235 U; reformulated as 238 U), an effective tracer of oceanic redox conditions, as a proxy for changes in the global proportion of anoxic seafloor. We present a new δ 238 U dataset for carbonate rocks from the Lower Nama Group, Namibia, deposited in a shelf ramp succession during the terminal Neoproterozoic (~550 to ~547 Ma). These data have persistently low δ 238 U (average =-0.81 ± 0.06‰) compared with the signature of modern day seawater. Such low δ 238 U are consistent with enhanced U drawdown from the water column under anoxic conditions, and the preferential export of 'heavy' 238 U to sediments following U(VI)-U(IV) reduction. Placing our results into a steady state ocean box model suggests at least a third of the global seafloor was covered by anoxic bottom waters compared with only 0.3% in today's oxygenated oceans. Comparison with δ 238 U from older sediments deposited in other basins further supports an expansion of anoxic bottom waters towards the end of the Ediacaran. Our data are consistent with an emerging picture of a dominantly anoxic Ediacaran ocean punctuated by brief ocean oxygenation events. In the Nama Group, the transition towards globally widespread anoxic conditions postdates the first appearance of both skeletal metazoans and softbodied fauna of the Nama Assemblage. This suggests that the global expansion of anoxia did not coincide with the decline of the Ediacaran biota, or drive the biotic turnover between the White Sea and Nama Assemblages. The impact of this global redox change on metazoan ecosystems is unclear, since the expansion of anoxia, if contained mainly within deeper waters, may not have impinged significantly upon continental shelves that host the majority of biodiversity.
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