BACTERIA/ARCHAEA
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The ANT-Biofilm research project (PNRA16_00105) concerned the study of microbial colonization processes in coastal environments of Terra Nova Bay (Ross Sea), through the analysis of the microbial biofilm (bacteria, microalgae) and macrobenthic settlement on plastic substrates, with the aim of determining their possible variations caused by natural or anthropogenic disturbances (variations in salinity or the presence of contaminants, respectively). Microbial biofilms, which play a key role as a substrate for larval settlement of many species of invertebrates, constitute hot-spots of microbial diversity; and it is also known that the communities a microbial are capable of responding rapidly to changing environmental conditions, acting as potential "sentinels" of natural or anthropic perturbations that recently are threatening the Antarctic biota. During the first year of activity (XXXIII Italian expedition, November 2017) stainless steel structures were fixed on the seabed of Road Bay and Tethys Bay mounting panels of artificial substrates (Polyvinyl Chloride, PVC and PolyEthylene, PE) for colonization, which during the XXXIV expedition (November 2018) were retrieved in order to study the fouling formation processes at different levels of biological complexity (from microbial community including bacteria and microalgae to benthic invertebrates) and to evaluate their evolution in two coastal sites differently exposed to natural or anthropogenic forcings.
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We will collect stool samples from the volunteers at the Mario Zucchelli Station at different time points. The samples will be analysed by shotgun metagenomic sequencing, considering only the microbial component.
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We will collect oral samples from the volunteers at the Mario Zucchelli Station at different time points, using safe and not harmfull kits. Samples will be analysed by shotgun metagenomic sequencing, considering only the microbial component.
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We will collect skin samples from the volunteers at the Mario Zucchelli Station at different time points, using safe and not harmfull kits. Samples will be analysed by shotgun metagenomic sequencing, considering only the microbial component.