Bacterial succession across seasonal transitions in the coastal waters of the western Antarctic Peninsula

The marine ecosystem west of the Antarctic Peninsula (WAP) undergoes a dramatic seasonal transition every spring, from almost total darkness to almost continuous sunlight, resulting in a cascade of environmental changes, including the intense phytoplankton blooms that support a highly productive food web. Despite having important implications for the microbial loop and the biological carbon pump, the degree of trophic coupling between phytoplankton and bacteria is unclear. In particular, due to the difficulties inherent in sampling this remote system during the Antarctic winter and spring, little is known about how phytoplankton blooms may or may not drive bacterial seasonal succession. Using 16S rRNA gene amplicon sequencing, we assessed bacterial community composition in 68 samples from 24 dates that spanned the cold, dark winter, spring transitional period, and summer phytoplankton bloom. Our analysis resulted in 15 million sequences and 12,000 Operational Taxonomic Units (OTUs). We found that mid-winter bacterial communities had the highest richness (~1,800 observed OTUs in rarefied libraries) and a greater abundance of oligotrophic and potentially chemoautolithotrophic taxa. The bacterial community changed only gradually up until the onset of a mid-summer phytoplankton bloom, which coincided with a 100-fold increase in bacterial production, a rapid decline in richness to ~700 OTUs, and a shift in community composition toward copiotrophic taxa. This period lasted only a few weeks, at the end of which the bacterial community had largely reverted to its mid-winter state. Our findings provide new evidence of trophic coupling between bacteria and phytoplankton and highlight the importance of higher-resolution time series sampling in order to capture rapid seasonal changes.