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Microbial communities (Bacteria and Archaea) in Lake Fryxell (Antarctica) along an oxygen gradient

Citation

Jungblut A, Hawes I, Mackey T, Krusor M, Doran P, Sumner D, Eiser J, Hillman C, Goroncy A, Sweetlove M (2019). Microbial communities (Bacteria and Archaea) in Lake Fryxell (Antarctica) along an oxygen gradient. Version 1.1. SCAR - Microbial Antarctic Resource System. Metadata dataset https://doi.org/10.15468/we8w77 accessed via GBIF.org on 2023-03-25.

Description

Amplicon sequencing dataset (MiSeq) of Archaea and Bacteria (16S ssu rRNA) in microbial mats at the floor of lake Fryxell (Antarctica).

Sampling Description

Study Extent

Microbial mat samples representing the main three macroscopic mat morphologies, i.e., cuspate pinnacle, ridge-pit, and prostrate were collected from the floor of Lake Fryxell in November 2012.

Sampling

Samples were collected by a diver by cutting squares of mat from the lake floor and gently lifting them into a plastic box previously cleaned with antibacterial wipes. Box lids were sealed under water and samples returned to the surface and transferred to lakeside laboratory, where they were immediately dissected using flame-sterilized blades and forceps. Pinnacle and ridge-pit mats were dissected according to their distinctively pigmented horizontal upper (pink-purple and brown-purple, respectively), middle (pale purple and green-beige, respectively), and lower (all beige) layers. Prostrate mats were similarly dissected into upper (brown-purple), middle (green- beige), and lower (beige) layers. Dissected subsamples were rinsed in ster- ile deionized water, transferred into sterile plastic tubes, and frozen at 20°C until further analysis.

Method steps

  1. DNA extractions of each of the triplicate mat sections were performed using the MoBio PowerDNA biofilm kit according to the manufacturer’s instructions. DNA was quantified using a Qubit fluorometer, and equal amounts of DNA per sample were pooled for 16S rRNA gene amplification. 16S rRNA gene PCR products were amplified in triplicate, pooled, and cleaned using the MoBio UltraClean PCR clean-up kit ac- cording to the manufacturer’s instructions. For the high-throughput se- quencing, we used primers (515f and 806r), described by Caporaso et al., which amplify both archaeal and bacterial 16S rRNA genes, including cyanobacterial 16S rRNA genes.
  2. Sequencing was performed on a MiSeq Illumina sequencer at NZ Genomics Limited, Palmerston North, New Zealand.

Taxonomic Coverages

Archaea and Bacteria (16S ssu rRNA gene)
  1. Bacteria
    common name: Bacteria rank: domain
  2. Archaea
    common name: Archaea rank: domain

Geographic Coverages

Lake Fryxell, Antarctica

Bibliographic Citations

  1. Jungblut, A. D., Hawes, I., Mackey, T. J., Krusor, M., Doran, P. T., Sumner, D. Y., ... & Goroncy, A. K. (2016). Microbial mat communities along an oxygen gradient in a perennially ice-covered Antarctic lake. Appl. Environ. Microbiol., 82(2), 620-630. -

Contacts

Anne Jungblut
originator
The Natural History Museum
London
GB
Ian Hawes
originator
University of Canterbury
Christchurch
NZ
Tyler Mackey
originator
University of California
Davis
US
Megan Krusor
originator
University of California
Davis
US
Peter Doran
originator
Louisiana State University
Baton Rouge
US
Dawn Sumner
originator
University of California
Davis
US
Jonathan Eiser
originator
University of California
Davis
US
Colin Hillman
originator
University of Canterbury
Christchurch
NZ
Alexander Goroncy
originator
University of Canterbury
Christchurch
NZ
Maxime Sweetlove
metadata author
position: Assistent researcher
Royal Belgian Institute of Natural Sciences
Brussels
1000
BE
email: msweetlove@naturalsciences.be
Anne Jungblut
administrative point of contact
The Natural History Museum
London
GB
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