The face of Planet Earth has changed significantly through geological time. Dynamic processes active today, such as plate tectonics and climate change, have shaped the Earth’s surface and impacted biodiversity patterns from the beginning. Organisms, on the other hand, have the capacity to significantly alter Earth’s hydrological and geochemical cycles, its atmosphere and climate, sediments, and even hard rocks deep down under the surface. Abiotic– biotic interactions characterize Earth’s system history and, together with biotic competition and food webs, were the main trigger of evolutionary change, innovations and biodiversity fluctuations. Within the Palaeozoic, the Devonian was an especially interesting time interval as it was characterized by the ‘mid-Paleozoic predator revolution’ (Signor & Brett 1984; Brett 2003) and the related ‘nekton revolution’ (Klug et al. 2010), characterized by the blooms of free-swimming cephalopods, including the oldest ammonoids, and fish groups (e.g. toothed sharks and giant placoderms), the rise of more advanced vertebrates, including the oldest tetrapods (e.g. Blieck et al. 2007, 2010; Niedzwiedzki et al. 2010), the most extensive reef complexes of the Phanerozoic (e.g. Kiessling 2008), and the ‘greening of land’ by the diversification and spread of land plants, including the oldest forests (e.g. Stein et al. 2012; Giesen & Berry 2013), which resulted in new soil types and changing weathering. These major evolutionary trends did not unfold in a long interval of environmental stability, but in times of numerous and repeated, geologically brief, global events that punctuated prolonged periods, up to several million years in duration, of relative stability, termed ecological-evolutionary subunits (EE subunits: Boucot 1990; Brett & Baird 1995; Brett et al. 2009). The bounding events, even those of lesser intensity, produced major re-structuring in local to global ecosystems and are seen as critical drivers of long-term evolutionary patterns (Brett 2012). These linked abiotic and biotic events and extinctions of different magnitude have been summarized by House (1983, 1985, 2002), Walliser (1984, 1996) and, more recently, by Becker et al. (2012). The Devonian event succession is summarized in Figure 1. Two first-order mass extinctions at the Frasnian–Famennian boundary (Kellwasser Crisis) and at the end of the Devonian (Hangenberg Crisis), characterized by the loss of major fossil groups (classes and orders) and complete ecosystems (e.g. metazoan reefs, early forests), have to be viewed in the context of a complex global event sequence. There are important similarities between discrete pulses/phases of the major biotic crises and individual smaller-scale events. In our understanding, second-order global events are characterized by sudden extinctions in many groups and ecosystems, including the complete disappearance of several widespread and diverse organism groups (orders and families). Examples are the basal Emsian atopus Event, where the planktonic graptolites finally died out, the Taghanic Crisis, Frasnes events and Lower Kellwasser Event. Third-order global events show globally elevated extinction rates, often at lower taxonomic level (genera and species), but within many clades and in several ecosystems. Examples are the Silurian–Devonian boundary Klonk Event, and the Daleje, Chotěc, Kacak, Condroz and Annulata events. Fourth-order global extinctions refer to the sudden disappearance of relatively fewer but widespread groups, which implies a global, not regional, trigger. This category may include the Lochkovian–Pragian boundary
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Jul 6, 2017
Zofia Dubicka 
Open Access