The two phases of the Cambrian Explosion

Abstract The dynamics of how metazoan phyla appeared and evolved – known as the Cambrian Explosion – remains elusive. We present a quantitative analysis of the temporal distribution (based on occurrence data of fossil species sampled in each time interval) of lophotrochozoan skeletal species (n = 430) from the terminal Ediacaran to Cambrian Stage 5 (~545 – ~505 Million years ago (Ma)) of the Siberian Platform, Russia. We use morphological traits to distinguish between stem and crown groups. Possible skeletal stem group lophophorates, brachiopods, and molluscs (n = 354) appear in the terminal Ediacaran (~542 Ma) and diversify during the early Cambrian Terreneuvian and again in Stage 2, but were devastated during the early Cambrian Stage 4 Sinsk extinction event (~513 Ma) never to recover previous diversity. Inferred crown group brachiopod and mollusc species (n = 76) do not appear until the Fortunian, ~537 Ma, radiate in the early Cambrian Stage 3 (~522 Ma), and with minimal loss of diversity at the Sinsk Event, continued to diversify into the Ordovician. The Sinsk Event also removed other probable stem groups, such as archaeocyath sponges. Notably, this diversification starts before, and extends across the Ediacaran/Cambrian boundary and the Basal Cambrian Carbon Isotope Excursion (BACE) interval (~541 to ~540 Ma), ascribed to a possible global perturbation of the carbon cycle. We therefore propose two phases of the Cambrian Explosion separated by the Sinsk extinction event, the first dominated by stem groups of phyla from the late Ediacaran, ~542 Ma, to early Cambrian stage 4, ~513 Ma, and the second marked by radiating bilaterian crown group species of phyla from ~513 Ma and extending to the Ordovician Radiation

Low-oxygen waters limited habitable space for early animals

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

Coupling of ocean redox and animal evolution during the Ediacaran-Cambrian transition

The late Ediacaran to early Cambrian interval witnessed extraordinary radiations of metazoan life. The role of the physical environment in this biological revolution, such as changes to oxygen levels and nutrient availability, has been the focus of longstanding debate. Seemingly contradictory data from geochemical redox proxies help to fuel this controversy. As an essential nutrient, nitrogen can help to resolve this impasse by establishing linkages between nutrient supply, ocean redox, and biological changes. Here we present a comprehensive N-isotope dataset from the Yangtze Basin that reveals remarkable coupling between δ¹⁵N, δ¹³C, and evolutionary events from circa 551 to 515 Ma. The results indicate that increased fixed nitrogen supply may have facilitated episodic animal radiations by reinforcing ocean oxygenation, and restricting anoxia to near, or even at the sediment–water interface. Conversely, sporadic ocean anoxic events interrupted ocean oxygenation, and may have led to extinctions of the Ediacaran biota and small shelly animals

New trilobite assemblage from the lower Cambrian (upper Stage 4) of the Lake Zone, western Mongolia

The western Mongolian Lake Zone was a Neoproterozoic to early Paleozoic volcanic arc where tuffs, lavas, fossiliferous siliciclastics, and carbonates accumulated during the early Cambrian. An uppermost Cambrian Series 2 (upper Stage 4) trilobite assemblage is described here from the Burgasutay Formation representing a continuous lower Cambrian succession at the Seer Ridge of the Great Lake Depression. The new assemblage is dominated by dorypygids and consists of 13 trilobite genera belonging to nine families including Catinouyia heyunensis new species. These fossils comprise the youngest and richest lower Cambrian trilobite assemblage in Mongolia. The composition of the Lake Zone fauna suggests its biogeographic affinity with the Siberian Platform and Altay-Sayan Foldbelt, but the presence of inouyiids also implies a connection of this region with East Gondwana. UUID: http://zoobank.org/fb0ebe23-144f-46ed-9543-7df9eea85fb

Calibrating the temporal and spatial dynamics of the Ediacaran - Cambrian radiation of animals

The Ediacaran-Cambrian transition, which incorporates the radiation of animals, lacks a robust global temporal and spatial framework, resulting in major uncertainty in the evolutionary dynamics of this critical radiation and its relationship to changes in palaeoenvironmental geochemistry. We first present a new δ13Ccarb composite reference curve for the Ediacaran Nama Group of southern Namibia, and we then outline four new possible global age models (A to D) for the interval 551–517 million years ago (Ma). These models comprise composite carbonate‑carbon isotope (δ13Ccarb) curves, which are anchored to radiometric ages and consistent with strontium isotope chemostratigraphy, and are used to calibrate metazoan distribution in space and time. These models differ most prominently in the temporal position of the basal Cambrian negative δ13Ccarb excursion (BACE). Regions that host the most complete records show that the BACE nadir always predates the Ediacaran-Cambrian boundary as defined by the first appearance datum (FAD) of the ichnospecies Treptichnus pedum. Whilst treptichnid traces are present in the late Ediacaran fossil record, the FAD of the ichnospecies T. pedum appears to post-date the last appearance datums (LADs) of in situ representatives of the skeletal organisms Cloudina and Namacalathus in all environments with high-resolution δ13Ccarb data. Two age models (A and B) place the BACE within the Ediacaran, and yield an age of ~538.8 Ma for the Ediacaran-Cambrian boundary; however models C and D appear to be the most parsimonious and may support a recalibration of the boundary age by up to 3 Myr younger. All age models reveal a previously underappreciated degree of variability in the terminal Ediacaran, incorporating notable positive and negative excursions that precede the BACE. Nothwithstanding remaining uncertainties in chemostratigraphic correlation, all models support a pre-BACE first appearance of Cambrian-type shelly fossils in Siberia and possibly South China, and show that the Ediacaran-Cambrian transition was a protracted interval represented by a series of successive radiations