Diatom sedimentary ancient DNA metabarcoding from western Fram Strait and Kronotsky Peninsula

• Main Authors: Zimmermann, Heike, Stoof-Leichsenring, Kathleen R., Kruse, Stefan, Müller, Juliane, Stein, Ruediger, Tiedemann, Ralf, Herzschuh, Ulrike
• Format: Dataset
• Language: unknown
• Published: 2020
• Subjects: Pacific; Fram Strait; Kamchatka; North Atlantic; Subarctic
• Online Access: https://zenodo.org/record/3998282; https://doi.org/10.5061/dryad.bnzs7h481

In this study we use sedimentary ancient DNA metabarcoding from two marine sediment cores. The first Kastenlot core MSM05/5-712-2 was taken at western Fram Strait (subarctic North Atlantic) from which we collected 12 samples including one biological replicate. The second Kastenlot core SO201-2-12KL was retrieved from Kamchatka Strait (subarctic North Pacific) from which we collected 9 samples and 2 samples were collected from a pilot core taken next to the Kastenlot core. Total DNA was extracted from approximately 2ml sediment per sample in 3 batches with up to 9 samples and one extraction blank. Total DNA was concentrated and if necessary diluted to 2.5 ng/µl. For each batch we performed PCRs in triplicates including a PCR no template control (NTC). We amplified a diatom-specific, 76 bp long part of the rbcL gene with tagged primers Diat_rbcL_705F (AACAGGTGAAGTTAAAGGTTCATAYTT) and Diat_rbcL_808R (TGTAACCCATAACTAAATCGATCAT). The PCR-products were purified and pooled in equal concentrations. The sequencing library was prepared with the Mid Output kit v. 2 according to the Fasteris Metafast protocol for low complexity amplicon sequencing and checked by qPCR. The library was sequenced (2 x 150 bp, paired-end) on the Illumina NextSeq 500 at the Fasteris SA sequencing service (Switzerland). For two samples we sequenced 4 PCR-products and for two samples we could only get 2 PCR-products with sufficient DNA content for sequencing. Funding provided by: European Research CouncilCrossref Funder Registry ID: http://dx.doi.org/10.13039/501100000781 Here, we provide the raw paired-end sequencing data received from Fasteris as gz-compressed fastq files (frorward reads: 190128_NB501850_A_L1-4_AGAK-6_R1.fastq.gz; reverse reads: 190128_NB501850_A_L1-4_AGAK-6_R2.fastq.gz). Data processing, which includes assignment of the sequencing reads to the different samples with a tagfile (tagfile_AGAK-6.txt), denoising and taxonomic assignment of reads, was performed with the OBITools pipeline ...