The DOI matches its Crossref record; 5 of the 5 references it cites were found in a registry or an index.
Phylogenomics and the evolution of hemipteroid insects
Open accessAbstract
Hemipteroid insects (Paraneoptera), with over 10% of all known insect diversity, are a major component of terrestrial and aquatic ecosystems. Previous phylogenetic analyses have not consistently resolved the relationships among major hemipteroid lineages. We provide maximum likelihood-based phylogenomic analyses of a taxonomically comprehensive dataset comprising sequences of 2,395 single-copy, protein-coding genes for 193 samples of hemipteroid insects and outgroups. These analyses yield a well-supported phylogeny for hemipteroid insects. Monophyly of each of the three hemipteroid orders (Psocodea, Thysanoptera, and Hemiptera) is strongly supported, as are most relationships among suborders and families. Thysanoptera (thrips) is strongly supported as sister to Hemiptera. However, as in a recent large-scale analysis sampling all insect orders, trees from our data matrices support Psocodea (bark lice and parasitic lice) as the sister group to the holometabolous insects (those with complete metamorphosis). In contrast, four-cluster likelihood mapping of these data does not support this result. A molecular dating analysis using 23 fossil calibration points suggests hemipteroid insects began diversifying before the Carboniferous, over 365 million years ago. We also explore implications for understanding the timing of diversification, the evolution of morphological traits, and the evolution of mitochondrial genome organization. These results provide a phylogenetic framework for future studies of the group.
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Cites
Phylogenomics resolves the timing and pattern of insect evolution
Misof, B., Liu, S., Meusemann, K., Peters, R. S., Donath, A., Mayer, C., Frandsen, P. B., Ware, J., Flouri, T., Beutel, R. G., et al. (2014) · Science · doi:10.1126/science.1257570 · Cited by 2,694
Self-citationBest Practices for Justifying Fossil Calibrations
Parham, J. F., Donoghue, P. C. J., Bell, C. J., Calway, T. D., Head, J. J., Holroyd, P. A., Inoue, J. G., Irmis, R. B., Joyce, W. G., Ksepka, D. T., et al. (2012) · Systematic Biology · doi:10.1093/sysbio/syr107 · Cited by 780
Selecting optimal partitioning schemes for phylogenomic datasets
Lanfear, R., Calcott, B., Kainer, D., Mayer, C., & Stamatakis, A. (2014) · BMC Evolutionary Biology · doi:10.1186/1471-2148-14-82 · Cited by 762
Self-citationInferring ancient divergences requires genes with strong phylogenetic signals
Salichos, L., & Rokas, A. (2013) · Nature · doi:10.1038/nature12130 · Cited by 616
Contentious relationships in phylogenomic studies can be driven by a handful of genes
Shen, X.-X., Hittinger, C. T., & Rokas, A. (2017) · Nature Ecology & Evolution · doi:10.1038/s41559-017-0126 · Cited by 520
Cited by
Fernandez-Nicolas, A., Machaj, G., Ventos-Alfonso, A., Pagone, V., Minemura, T., Ohde, T., Daimon, T., Ylla, G., & Belles, X. (2023) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.2216640120 · Cited by 37
Brochosomes as an antireflective camouflage coating for leafhoppers
Wu, W., Mao, Q., Ye, Z.-X., Liao, Z., Shan, H.-W., Li, J.-M., Zhang, C.-X., & Chen, J.-P. (2025) · eLife · doi:10.7554/elife.99639.3 · Cited by 3
Metadata
- Authors
- Johnson, K. P., Dietrich, C. H., Friedrich, F., Beutel, R. G., Wipfler, B., Peters, R. S., Allen, J. M., Petersen, M., Donath, A., Walden, K. K. O., Kozlov, A. M., Podsiadlowski, L., Mayer, C., Meusemann, K., Vasilikopoulos, A., Waterhouse, R. M., Cameron, S. L., Weirauch, C., Swanson, D. R., Percy, D. M., Hardy, N. B., Terry, I., Liu, S., Zhou, X., Misof, B., Robertson, H. M., & Yoshizawa, K.
- Venue
- Proceedings of the National Academy of Sciences
- Published
- 2018-11-26
- Volume
- 115
- Issue
- 50
- Pages
- 12775-12780
- ISSN
- 0027-8424 (ISSN-L)
- 1091-6490
- OpenAlex
- W2902515710
- Cited by
- 389
- References
- 5
- FWCI
- 27.81
- Type
- journal article
- Language
- en
- Open access
- bronze
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