Microbes residing in cryoconite holes (debris, water, and nutrient-rich ecosystems) on the glacier surface actively participate in carbon and nutrient cycling. Not much is known about how these communities and their functions change during the summer melt-season when intense ablation and runoff alter the influx and outflux of nutrients and microbes. Here, we use high-throughput-amplicon sequencing, predictive metabolic tools and Phenotype MicroArray techniques to track changes in bacterial communities and functions in cryoconite holes in a coastal Antarctic site and the surrounding fjord, during the summer season. The bacterial diversity in cryoconite hole meltwater was predominantly composed of heterotrophs (Proteobacteria) throughout the season. The associated functional potentials were related to heterotrophic-assimilatory and -dissimilatory pathways. Autotrophic Cyanobacterial lineages dominated the debris community at the beginning and end of summer, while heterotrophic Bacteroidota- and Proteobacteria-related phyla increased during the peak melt period. Predictive functional analyses based on taxonomy show a shift from predominantly phototrophy-related functions to heterotrophic assimilatory pathways as the melt-season progressed. This shift from autotrophic to heterotrophic communities within cryoconite holes can affect carbon drawdown and nutrient liberation from the glacier surface during the summer. In addition, the flushing out and export of cryoconite hole communities to the fjord could influence the biogeochemical dynamics of the fjord ecosystem.
Mangrove sediment microorganisms play a vital role in the
energy transformation and element cycling in marine wetland
ecosystems. Using metagenomics analysis strategy, we
compared the taxonomic structure and gene profile of the
mangrove and non-mangrove sediment samples at the subtropical
estuary in Beibu Gulf, South China Sea. Proteobacteria,
Bacteroidetes, and Firmicutes were the most abundant
bacterial phyla. Archaeal family Methanosarcinaceae
and bacterial genera Vibrio and Dehalococcoides were significantly
higher in the mangrove sediments than in the nonmangrove
sediments. Functional analysis showed that “Carbohydrate
metabolism” was the most abundant metabolic
category. The feature of carbohydrate-active enzymes (CZs)
was analyzed using the Carbohydrate-Active EnZymes Database.
The significant differences of CZs between mangrove
and non-mangrove sediments, were attributed to the amounts
of polyphenol oxidase (EC 1.10.3.-), hexosyltransferase (EC
2.4.1.-), and β-N-acetylhexosaminidase (EC 3.2.1.52), which
were higher in the mangrove sediment samples. Principal
component analysis indicated that the microbial community
and gene profile between mangrove and non-mangrove sediments
were distinct. Redundancy analysis showed that total
organic carbon is a significant factor that affects the microbial
community and gene distribution. The results indicated
that the mangrove ecosystem with massive amounts of organic
carbon may promote the richness of carbohydrate metabolism
genes and enhance the degradation and utilization
of carbohydrates in the mangrove sediments.