An extremely dynamic chain of archipelagos links South America and the Antarctic Peninsula. It includes islands, which are large and small, old and young, near continental margins and isolated, and well sampled and poorly known. The current study sampled the macrobenthos of all the major archipelagos of this arc at shelf and slope depths using an Agassiz trawl. At least four samples (200 m, 500 m, 1000 m and 1500 m) were taken down-slope at Falkland Trough, Shag Rocks, South Georgia, South Thule, Powell Basin, Elephant Island, and Livingston Island sites and one sample was collected in the caldera of Deception Island. Despite the biogeographical and biodiversity importance of this region, this is the first time (by definition) entire standardized trawl samples have been analysed from all its archipelagos and at any consistent taxonomic level. We found 15 phyla and 29 classes of macro- and megafauna in total across the samples, many of which occurred at all sites. Even at remote and geologically young sites richness was high. Richness increased with abundance and wet mass and was highest in the shallow shelf samples and lowest at 1500 m. Abundance and wet mass varied more than two orders of magnitude, even within classes or study areas. There were strong similarities between the ascidian dominated shallow faunas of the two active volcanic sites, Southern Thule and Deception Island despite huge differences in isolation. There were also strong faunal similarities between Falkland Trough and Shag Rocks despite being on opposing sides of the Polar Front. In contrast two near neighbours with similarly soft substrata, Elephant and Livingston islands were amongst the most dissimilar.

It has long been assumed that the extant bilaterian phyla generally have their origin in the Cambrian explosion, when they appear in an essentially modern form. Both these assumptions are questionable. A strict application of stem- and crown-group concepts to phyla shows that although the branching points of many clades may have occurred in the Early Cambrian or before, the appearance of the modern body plans was in most cases later: very few bilaterian phyla sensu stricto have demonstrable representatives in the earliest Cambrian. Given that the early branching points of major clades is an inevitable result of the geometry of clade diversification, the alleged phenomenon of phyla appearing early and remaining morphologically static is seen not to require particular explanation. Confusion in the definition of a phylum has thus led to attempts to explain (especially from a developmental perspective) a feature that is partly inevitable, partly illusory. We critically discuss models for Proterozoic diversification based on small body size, limited developmental capacity and poor preservation and cryptic habits, and show that the prospect of lineage diversification occurring early in the Proterozoic can be seen to be unlikely on grounds of both parsimony and functional morphology. Indeed, the combination of the body and trace fossil record demonstrates a progressive diversification through the end of the Proterozoic well into the Cambrian and beyond, a picture consistent with body plans being assembled during this time. Body-plan characters are likely to have been acquired monophyletically in the history of the bilaterians, and a model explaining the diversity in just one of them, the coelom, is presented. This analysis points to the requirement for a careful application of systematic methodology before explanations are sought for alleged patterns of constraint and flexibility.