“…The molecular terminals analyzed in this study and GenBank accession numbers corresponding to the gene fragments sequenced are listed in Supporting Information Table 1. For these analyses, the 94 novel DNA sequences were combined with 436 previously published DNA sequences from the following sources: (Alfaro et al, ; Betancur‐R, Broughton et al, ; Betancur‐R, Li, Munroe, Ballesteros, & Ortí, ; Bossu, Beaulieu, Ceas, & Near, ; Cawthorn, Steinman, & Witthuhn, ; Chang et al, ; Chen, Ruiz‐Carus, & Ortí, ; Davis et al, ; Dunlap et al, ; Durand et al, ; Holcroft & Wiley, ; Kenchington, Baillie, Kenchington, & Bentzen, ; Kimmerling et al, ; Li et al, ; Li, Ortí, & Zhao, ; Near et al, , , , ; Near & Keck, ; Rabosky et al, ; Sanciangco et al, ; Satoh, ; Satoh, Miya, Mabuchi, & Nishida, ; Smith et al, ; Smith, Smith, & Wheeler, ; Smith & Craig, ;Smith & Wheeler, , ; Sparks & Smith, ; Thacker et al, ; Tsunashima et al, ; Wainwright et al, ; Yagishita et al, ; Yamanoue et al, ; and 21 unpublished studies). The matrix was 70.4% complete at the amplicon level.…”