Abstract:

This dataset includes an inventory of processed, taxonomically classified bacterial amplicons from marsh water, a component of a longitudinal study of marsh microbial diversity and sediment stability before, during, and after oil deposition associated with the Deepwater Horizon oil spill. The goals of the dataset are 1) to assess and track bacterial community composition in Louisiana marshes over time and 2) to contribute to a biophysical model of marsh ecosystem processes in the context of petrogenic and biogenic hydrocarbon exposure.

Suggested Citation:

Engel, Annette S., Paterson, Audrey T. . 2016. October 2012 water column bacterial diversity data supporting changes in Louisiana marsh microbial communities after the Deepwater Horizon oil spill. Distributed by: GRIIDC, Harte Research Institute, Texas A&M University–Corpus Christi. doi:10.7266/N74F1NNW

Purpose:

454 tag pyrosequencing of the V1-V3 region of bacterial 16S rRNA genes from marsh water environmental samples supports the study of bacterial community diversity and function.

Data Parameters and Units:

Data are reported as classified 454 amplicon abundance. Latitude (decimal degrees N), Longitude (decimal degrees W), Collection Date (DD-MMM-YYYY), Sample Description, Geographic Location Name, Total Classified Amplicons

Methods:

Total nucleic acids were extracted from duplicate Sterives filters using the MoBio PowerWater Sterivex kits according to the manufacturer protocol (MoBio Laboratories Inc., Carlsbad, CA, USA). Amplification and pyrosequencing of the V1-V3 region of 16S rRNA genes were done using a 454 GS FLX Titanium (Roche, 454 Life Sciences, Branford, CT, USA) by the Molecular Research LP (Sweetwater, TX). Raw 16S rRNA gene sequences were processed using the microbial ecology community software Mothur (http://www.mothur.org/wiki/Download_mothur) (Schloss et al., 2011). Amplicons were trimmed for length (200-500bp) and quality (average quality score of 35 over a sliding window of 50bp), aligned and classified using the SILVA reference database (https://www.arb-silva.de/silva-license-information), screened and filtered, and removed of chimera detected by UCHIME (http://drive5.com/uchime)(Schloss et al., 2011). Inventories of processed reads classified at the phylum level and Proteobacterial classes are provided for each sample.

Instruments:

Pyrosequencing of the V1-V3 region of 16S rRNA genes was done using a 454 GS FLX Titanium (Roche, 454 Life Sciences, Branford, CT, USA) by the Molecular Research LP (Sweetwater, TX).

Individual Files: