Little is known about biological soil crust (BSC) formation during the early stages of primary succession following glacial retreat. Here, we report on focused sampling of twelve discrete BSC colonies near the snout of a retreating glacier in the High Arctic and show that BSC colonies had significantly higher 16S and 18S rRNA gene diversity than the simpler communities of bare sediments sampled next to each colony. Surprisingly, the colonies also had a higher degree of community dispersion than the more clustered bare sediment controls. There were only eight 16S amplicons that showed 100% prevalence in all 12 of the colonies, and the three most abundant of these keystone amplicons were cyanobacteria, including a nitrogen fixing Nostoc. The only 18S amplicon common to all colonies was a diatom related to Sellaphora. This prominence of phototrophs indicates that early-successional BSC colonies are being supported by photosynthesis rather than ancient- or aeolian-derived organic matter. Co-occurrence network analysis among the phototrophs and fungi identified several potential early-successional soil lichens. Overall, our fine-scaled sampling revealed new insights into community assembly and function in actual communities of interacting microbes (as opposed to mixed communities in bulk soil samples) during the early stages of primary succession. By sampling discrete microbial colonies, we demonstrate how microbial communities assemble on sediments of a recently uncovered glacial forefield in the High Arctic (Midtre Lov & eacute;nbreen, Svalbard).

Glacial retreat due to global warming is exposing large tracts of barren glacial sediments that are quickly colonized by CO2-fixing microbial communities that can constitute the climax community in many high-Arctic, alpine, and Antarctic environments. Despite the potential importance of these processes, little is known about microbial community successional dynamics and rates of carbon (C) sequestration in environments where higher plants are slow or unable to establish. We analyzed microbial community succession and C and N accumulation in newly exposed sediments along an Antarctic glacial chronosequence where moss and microbial autotrophs are the dominant primary producers. During the first 4 years of succession (0 to 40 m from the glacier) algae (including diatoms) were the most relatively abundant eukaryotes, but by the second phase studied (8 to 12 years) moss amplicon sequence variants (ASVs) dominated. The rise in moss coincided with a significant buildup of C and N in the sediments. The final two phases of the successional sequence (16 to 20 and 26 to 30 years) were marked by declines in microbial species richness and moss relative abundance, that coincided with significant decreases in both total C and N. These retrogressive declines coincided with a large increase in relative abundance of predatory Vampyrellidae suggesting a possible mechanism for retrogression in this and perhaps other terrestrial ecosystems at the edge of the cryosphere. These findings have implications for understanding CO2 sequestration and ecosystem succession in microbial-dominated regions of the cryobiosphere where large tracts of land are currently undergoing deglaciation.