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The end-Permian mass extinction was the most severe mass extinction event of the Phanerozoic and was followed by a several million-year delay in benthic ecosystem recovery. While much work has been done to understand biotic recovery in both the body and trace fossil records of the Early Triassic, almost no focus has previously been given to analyzing patterns in ecosystem engineering complexity as a result of the extinction drivers. Bioturbation is a key ecosystem engineering behavior in marine environments, as it results in changes to resource flows and the physical environment. Thus, the trace fossil record can be used to examine the effect of the end-Permian mass extinction on bioturbating ecosystem engineers. We present a dataset compiled from previously published literature to analyze burrowing ecosystem engineering behaviors through the Permian-Triassic boundary. We report two key observations: first, that there is no loss in bioturbation ecosystem engineering behaviors after the mass extinction, and second, that these persisting behaviors include deep tier, high-impact, complex ecosystem engineering. These findings suggest that while environmental conditions may have limited deeper burrowing, complex ecosystem engineering behaviors were able to persist in the Early Triassic. Furthermore, the persistence of deep tier bioirrigated three-dimensional network burrows implies that benthic biogeochemical cycling could have been maintained at pre-extinction states in some local environments, stimulating ecosystem productivity and promoting biotic recovery in the Early Triassic.

The disappearance of the soft-bodied Ediacara biota at the Ediacaran–Cambrian boundary potentially represents the earliest mass extinction of complex life, although the precise driver(s) of this extinction remain unresolved. The ‘biotic replacement’ model proposes that an evolutionary radiation of metazoan ecosystem engineers in the latest Ediacaran profoundly altered marine palaeoenvironments, resulting in the extinction of Ediacara biota and setting the stage for the subsequent Cambrian Explosion. However, metazoan ecosystem engineering across the Ediacaran–Cambrian transition has yet to be quantified. Here, we test this key tenet of the biotic replacement model by characterizing the intensity of metazoan bioturbation and ecosystem engineering in trace fossil assemblages throughout the latest Ediacaran Nama Group in southern Namibia. The results illustrate a dramatic increase in both bioturbation and ecosystem engineering intensity in the latest Ediacaran, prior to the Cambrian boundary. Moreover, our analyses demonstrate that the highest-impact ecosystem engineering behaviours were present well before the onset of the Cambrian. These data provide the first support for a fundamental prediction of the biotic replacement model, and evidence for a direct link between the early evolution of ecosystem engineering and the extinction of the Ediacara biota.

The Ediacaran–Cambrian transition marks one of the most important geobiological revolutions in Earth History, including multiple waves of evolutionary radiation and successive episodes of apparent mass extinction. Among the proposed drivers of these events (in particular the extinction of the latest Neoproterozoic ‘Ediacara biota’) is the emergence of complex metazoans and their associated behaviors. Many metazoans are thought to have crucial geobiological impacts on both resource availability and the character of the physical environment – ‘ecosystem engineering’ – biological processes best preserved in the geological record as trace fossils. Here, we review this model using the trace fossil record of the Ediacaran to Cambrian Nama Group of southern Namibia, combining previous published accounts with the results of our own field investigations. We produce a revised ichnostratigraphy for the Nama Group that catalogues new forms, eliminates others, and brings the trace fossil record of the Nama into much closer alignment with what is known from other Ediacaran sections worldwide. We provide evidence for a link between sequence stratigraphy, oxygen, and the emergence of more complex bilaterian behaviors. Lastly, we show that observed patterns of extinction and survival over pulses of Ediacaran extinction are hard to ally with any one specific source of ecological stress associated with bioturbation, and thus a biologically-driven extinction of the Ediacara biota, if it occurred, was more likely to have been driven by some combination of these factors, rather than any single one.