The three redwood subfamily genera are Sequoia from coastal California and Oregon, Sequoiadendron from California's Sierra Nevada, and MetasequoiainChina. The redwood species contains the largest and tallest trees in the world. These trees can live for thousands of years. Threats include logging, fire suppression,[1] illegal marijuana cultivation, and burl poaching.[2][3]
Only two of the genera, Sequoia and Sequoiadendron, are known for massive trees. Trees of Metasequoia, from the single living species Metasequoia glyptostroboides, are deciduous, grow much smaller (although are still large compared to most other trees) and can live in colder climates.[citation needed]
Multiple studies of both morphological and molecular characters have strongly supported the assertion that the Sequoioideae are monophyletic.[4][5][6][7] Most modern phylogenies place Sequoia as sister to Sequoiadendron and Metasequoia as the out-group.[5][7][8] However, Yang et al. went on to investigate the origin of a peculiar genetic component in Sequoioideae, the polyploidyofSequoia—and generated a notable exception that calls into question the specifics of this relative consensus.[7]
A 2021 study using molecular evidence found the same relationships among Sequoioideae species, but found Sequoioideae to be the sister group to the Athrotaxidoideae (a superfamily presently known only from Tasmania) rather than to Taxodioideae. Sequoioideae and Athrotaxidoideae are thought to have diverged from each other during the Jurassic.[10]
Reticulate evolution refers to the origination of a taxon through the merging of ancestor lineages.
Polyploidy has come to be understood as quite common in plants—with estimates ranging from 47% to 100% of flowering plants and extant ferns having derived from ancient polyploidy.[11] Within the gymnosperms however it is quite rare. Sequoia sempervirensishexaploid (2n= 6x= 66). To investigate the origins of this polyploidy Yang et al. used two single copy nuclear genes, LFY and NLY, to generate phylogenetic trees. Other researchers have had success with these genes in similar studies on different taxa.[7]
Several hypotheses have been proposed to explain the origin of Sequoia's polyploidy: allopolyploidybyhybridization between Metasequoia and some probably extinct taxodiaceous plant; Metasequoia and Sequoiadendron, or ancestors of the two genera, as the parental species of Sequoia; and autohexaploidy, autoallohexaploidy, or segmental allohexaploidy.[citation needed]
Yang et al. found that Sequoia was clustered with Metasequoia in the tree generated using the LFY gene but with Sequoiadendron in the tree generated with the NLY gene. Further analysis strongly supported the hypothesis that Sequoia was the result of a hybridization event involving Metasequoia and Sequoiadendron. Thus, Yang et al. hypothesize that the inconsistent relationships among Metasequoia, Sequoia, and Sequoiadendron could be a sign of reticulate evolutionbyhybrid speciation (in which two species hybridize and give rise to a third) among the three genera. However, the long evolutionary history of the three genera (the earliest fossil remains being from the Jurassic) make resolving the specifics of when and how Sequoia originated once and for all a difficult matter—especially since it in part depends on an incomplete fossil record.[8]
Sequoioideae is an ancient taxon, with the oldest described Sequoioideae species, Sequoia jeholensis, recovered from Jurassic deposits.[12][13] The fossil wood Medulloprotaxodioxylon, reported from the late Triassic of China, resembles Sequoiadendron giganteum and may represent an ancestral form of the Sequoioideae; this supports the idea of a Late Triassic Norian origin for this subfamily.[14]
The fossil record shows a massive expansion of range in the Cretaceous and dominance of the Arcto-Tertiary Geoflora, especially in northern latitudes. Genera of Sequoioideae were found in the Arctic Circle, Europe, North America, and throughout Asia and Japan.[15] A general cooling trend beginning in the late Eocene and Oligocene reduced the northern ranges of the Sequoioideae, as did subsequent ice ages.[16] Evolutionary adaptations to ancient environments persist in all three species despite changing climate, distribution, and associated flora, especially the specific demands of their reproduction ecology that ultimately forced each of the species into refugial ranges where they could survive.[citation needed]
The extinct genus Austrosequoia, known from the Late Cretaceous-Oligocene of the Southern Hemisphere, including Australia and New Zealand, has been suggested as a member of the subfamily.[17]
Young but already tall redwood trees (Sequoia sempervirens) in Oakland, California
In 2024, it was estimated that there were about 500,000 redwoods in Britain, mostly brought as seeds and seedlings from the US in the Victorian era.[18] The entire subfamily is endangered. The IUCN Red List Category & Criteria assesses Sequoia sempervirens as Endangered (A2acd), Sequoiadendron giganteum as Endangered (B2ab) and Metasequoia glyptostroboides as Endangered (B1ab). In 2024 it was reported that over a period of two years about one-fifth of all giant sequoias were destroyed in extreme wildfires in California.[19]
^Kurland, Justin; Pires, Stephen F; Marteache, Nerea (2018). "The spatial pattern of redwood burl poaching and implications for prevention". Forest Policy and Economics. 94: 46–54. doi:10.1016/j.forpol.2018.06.009. S2CID158505170.
^Brunsfeld, Steven J; Soltis, Pamela S; Soltis, Douglas E; Gadek, Paul A; Quinn, Christopher J; Strenge, Darren D; Ranker, Tom A (1994). "Phylogenetic Relationships Among the Genera of Taxodiaceae and Cupressaceae: Evidence from rbcL Sequences". Systematic Botany. 19 (2): 253. doi:10.2307/2419600. JSTOR2419600.
^Takaso, T.; Tomlinson, P.B. (1992). "Seed cone and ovule ontogeny in Metasequoia, Sequoia and Sequoiadendron (Taxodiaceae-Coniferales)". Botanical Journal of the Linnean Society. 109: 15–37. doi:10.1111/j.1095-8339.1992.tb00256.x.
^ abcdYang, Z.Y.; Ran, J.H.; Wang, X.Q. (2012). "Three Genome-based Phylogeny of Cupressaceae s.l: Further Evidence for the Evolution of Gymnosperms and Southern Hemisphere Biogeography". Molecular Phylogenetics and Evolution. 64 (3): 452–470. doi:10.1016/j.ympev.2012.05.004. PMID22609823.
^Wan, Mingli; Yang, Wan; Tang, Peng; Liu, Lujun; Wang, Jun (2017). "Medulloprotaxodioxylon triassicum gen. Et sp. Nov., a taxodiaceous conifer wood from the Norian (Triassic) of northern Bogda Mountains, northwestern China". Review of Palaeobotany and Palynology. 241: 70–84. doi:10.1016/j.revpalbo.2017.02.009.
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