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33. Engl, E. & Attwell, D. Non-signalling energy use in the brain. J Physiol 593, 3417–3429, doi:10.1113/jphysiol.2014.282517 (2015).

ГЛАВА 4. ЧЕГО НИ СДЕЛАЕШЬ РАДИ ЛЮБВИ

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8. Mable, B. K. & Otto, S. P. The evolution of life cycles with haploid and diploid phases. BioEssays 20, 453–462, doi:10.1002/(sici) 1521–1878 (199806) 20:63.0. Co;2-n (1998).

9. Bernstein, H., Byers, G. S. & Michod, R. E. Evolution of Sexual Reproduction: Importance of DNA Repair, Complementation, and Variation. The American Naturalist 117, 537–549, doi:10.1086/283734 (1981).

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12. Gilbert, S. F. & Barresi, M. J. F. Developmental biology (2016).

13. Lehtonen, J., Kokko, H. & Parker, G. A. What do isogamous organisms teach us about sex and the two sexes? Philos Trans R Soc Lond B Biol Sci 371, doi:10.1098/rstb.2015.0532 (2016).

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Часть II. Откуда взялись мы

ГЛАВА 5. СЛОЖЕНИЕ ДВИЖЕНИЯ

1. Simpson, A. G. & Roger, A. J. The real 'kingdoms' of eukaryotes. Curr Biol 14, R693–696, doi:10.1016/j.cub.2004.08.038 (2004).

2. Keeling, P. J. et al. The tree of eukaryotes. Trends Ecol Evol 20, 670–676, doi:10.1016/j.tree.2005.09.005 (2005).

3. Adl, S. M. et al. The new higher level classification of eukaryotes with emphasis on the taxonomy of protists. J Eukaryot Microbiol 52, 399–451, doi:10.1111/j.1550–7408.2005.00053.x (2005).

4. Stiller, J. W. et al. The evolution of photosynthesis in chromist algae through serial endosymbioses. Nat Commun 5, 5764, doi:10.1038/ncomms6764 (2014).

5. Bodyl, A., Mackiewicz, P. & Gagat, P. Organelle evolution: Paulinella breaks a paradigm. Curr Biol 22, R304–306, doi:10.1016/j.cub.2012.03.020 (2012).

6. Philippe, H. et al. Phylogenomics revives traditional views on deep animal relationships. Curr Biol 19, 706–712, doi:10.1016/j.cub.2009.02.052 (2009).

7. Nielsen, C. Six major steps in animal evolution: are we derived sponge larvae? Evol Dev 10, 241–257, doi:10.1111/j.1525-142X.2008.00231.x (2008).

8. Cavalier-Smith, T. Origin of animal multicellularity: precursors, causes, consequences-the choanoflagellate/sponge transition, neurogenesis and the Cambrian explosion. Philos Trans R Soc Lond B Biol Sci 372, doi:10.1098/rstb.2015.0476 (2017).

9. Fairclough, S. R., Dayel, M. J. & King, N. Multicellular development in a choanoflagellate. Curr Biol 20, R875–876, doi:10.1016/j.cub.2010.09.014 (2010).

10. Juliano, C. & Wessel, G. Developmental biology. Versatile germline genes. Science 329, 640–641, doi:10.1126/science.1194037 (2010).

11. Worheide, G. et al. Deep phylogeny and evolution of sponges (phylum Porifera). Adv Mar Biol 61, 1–78, doi:10.1016/B978-0-12-387787-1.00007–6 (2012).

12. Leininger, S. et al. Developmental gene expression provides clues to relationships between sponge and eumetazoan body plans. Nat Commun 5, 3905, doi:10.1038/ncomms4905 (2014).

13. Ereskovsky, A. V. et al. The Homoscleromorph sponge Oscarella lobularis, a promising sponge model in evolutionary and developmental biology: model sponge Oscarella lobularis. Bioessays 31, 89–97, doi:10.1002/bies.080058 (2009).

14. Sharp, K. H., Eam, B., Faulkner, D. J. & Haygood, M. G. Vertical transmission of diverse microbes in the tropical sponge Corticium sp. Appl Environ Microbiol 73, 622–629, doi:10.1128/AEM.01493–06 (2007).

15. Gilbert, S. F. & Barresi, M. J. F. Developmental biology (2016).

16. Collins, A. G. Phylogeny of Medusozoa and the evolution of cnidarian life cycles. Journal of Evolutionary Biology 15, 418–432, doi:10.1046/j.1420–9101.2002.00403.x (2002).

17. Telford, M. J., Budd, G. E. & Philippe, H. Phylogenomic Insights into Animal Evolution. Curr Biol 25, R876–887, doi:10.1016/j.cub.2015.07.060 (2015).

18. Finnerty, J. R. Cnidarians Reveal Intermediate Stages in the Evolution of Hox Clusters and Axial Complexity1. Integrative and Comparative Biology 41, 608–620, doi:10.1093/icb/41.3.608 (2015).

19. Adoutte, A. et al. The new animal phylogeny: reliability and implications. Proc Natl Acad Sci USA 97, 4453–4456, doi:10.1073/pnas.97.9.4453 (2000).

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