“…Upon receipt of the raw sequences, we used the FastX toolkit to visualize the data quality, specifically the quality scores, read length, per bp quality, and per read quality (Pearson, Wood, Zhang, & Miller, 1997). We merged the raw paired‐end reads with the software PEAR v 0.9.6 (Zhang, Kobert, Flouri, & Stamatakis, 2014) using a quality threshold (Phred score) of 10 for trimming the reads and detected sequence chimeras de novo using default parameters of the UCHIME algorithm (Edgar, Haas, Clemente, Quince, & Knight, 2011).…”