Gingko

''Ginkgo'' is a genus of non-flowering seed plants, assigned to the gymnosperms. The scientific name is also used as the English common name. The order to which the genus belongs, Ginkgoales, first appeared in the Permian, , and ''Ginkgo'' is now the only living genus within the order. The rate of evolution within the genus has been slow, and almost all its species had become extinct by the end of the Pliocene'', is found in the wild only in China, but is cultivated around the world. The relationships between ginkgos and other groups of plants are not fully resolved.

Prehistory

The ginkgo (''Ginkgo biloba'') is a living fossil, with fossils similar to the modern plant dating back to the Permian, 270 million years ago. The ancestor of the genus is estimated to have branched off from other gymnosperms about 325 million years ago, while the last common ancestor of today's only remaining species lived not earlier than 390,000 years ago. The closest living relatives of the clade are the cycads, which share with the extant ''G. biloba'' the characteristic of motile sperm. Motile sperm is believed to be a basal trait of green plants, as it is also present in all non-seed plants such as ferns and mosses, as well as most green algae, which are believed to be the base of the green plant clade, the group in which the last common ancestor of land plants emerged. Motile sperm have been lost in all seed plants except for the ginkgo and the cycads, making it a shared conserved trait—a plesiomorphy—and implying these two groups themselves form a clade, sharing a common ancestor also with the trait, which diverged early from the rest of the seed plant lineage.

The time of this divergence is estimated to be extremely ancient, dating to the early Carboniferous. Fossils attributable to the genus ''Ginkgo'' with reproductive organs similar to the modern species first appeared in the Middle Jurassic, and the genus diversified and spread throughout Laurasia during the Jurassic and Early Cretaceous. It declined in diversity as the Cretaceous progressed with the extinction of species such as '' Ginkgo huolinhensis'', and by the Palaeocene, only a few ''Ginkgo'' species, '' Ginkgo cranei'' and ''Ginkgo adiantoides'', remained in the Northern Hemisphere, while a markedly different (and poorly documented) form persisted in the Southern Hemisphere. At the end of the Pliocene everywhere except in a small area of central China, where the modern species survived. It is doubtful whether the Northern Hemisphere fossil species of ''Ginkgo'' can be reliably distinguished. Given the slow pace of evolution and morphological similarity between members of the genus, there may have been only one or two species existing in the Northern Hemisphere through the entirety of the Cenozoic: present-day ''G. biloba'' (including ''G. adiantoides'') and '' G. gardneri'' from the Palaeocene of Scotland.

At least morphologically, ''G. gardneri'' and the Southern Hemisphere species are the only known post-Jurassic taxa that can be unequivocally recognised. The remainder may have been ecotypes or subspecies. The implications would be that ''G. biloba'' had occurred over an extremely wide range, had remarkable genetic flexibility and, though evolving genetically, never showed much speciation. While it may seem improbable that a species may exist as a contiguous entity for many millions of years, many of the ginkgo's life-history parameters fit. It displays extreme longevity and a slow reproduction rate. Additionally, in Cenozoic and later times, the ginkgo's distribution is wide and apparently contiguous, although steadily contracting. The fossil record shows extreme ecological conservatism as the niche of the ginkgo is restricted to disturbed streamside environments. Royer et al. (2003), p. 91.

Modern-day ''G. biloba'' grows best in well-watered and drained environments, and the extremely similar fossil ''Ginkgo'' favoured similar environments. The sediment records at the majority of fossil ''Ginkgo'' localities indicate it grew primarily in disturbed environments along streams and levees. ''Ginkgo'' therefore presents an " ecological paradox" because, while it possesses some favourable traits for living in disturbed environments (clonal reproduction), many of its other life-history traits (slow growth, large seed size, late reproductive maturity) are the opposite of those exhibited by "younger", more-recently emerged plant species that thrive in disturbed settings.

Given the slow rate of evolution of the genus, it is possible that ''Ginkgo'' represents a pre-angiosperm strategy for survival in disturbed streamside environments. ''Ginkgo'' evolved in an era before angiosperms (flowering plants), when ferns, cycads, and cycadeoids dominated disturbed streamside environments, forming a low, open, shrubby canopy. The large seeds of ''Ginkgo'' and its habit of "bolting"—growing to a height of before elongating its side branches—may be adaptations to such an environment. Diversity in the genus ''Ginkgo'' dropped through the Cretaceous (along with that of ferns, cycads, and cycadeoids) at the same time the flowering plants were on the rise, which supports the notion that flowering plants, with their better adaptations to disturbance, displaced ''Ginkgo'' and its associates over time.

'' Trichopitys heteromorpha'' from the earliest Permian of France, is one of the earliest fossils ascribed to the Ginkgophyta. It had multiple-forked non-laminar leaves with cylindrical, thread-like ultimate divisions. ''Sphenobaiera'' (early Permian–Cretaceous) had wedge-shaped leaves divided into narrow dichotomously- veined lobes, lacking distinct petioles (leaf stalks). ''Baiera'' (Triassic–Jurassic) had similar multiple-lobed leaves but with petioles.

Phylogeny

, molecular phylogenetic studies have produced at least six different placements of ''Ginkgo'' relative to cycads, conifers, gnetophytes and angiosperms. The two most common are that ''Ginkgo'' is a sister to a clade composed of conifers and gnetophytes, and that ''Ginkgo'' and cycads form a clade within the gymnosperms. A 2013 study examined the reasons for the discrepant results and concluded that the best support was for the monophyly of ''Ginkgo'' and cycads.

Etymology

The genus name is a mis‐transliteration of the Japanese pronunciation for the kanji . This name is adopted from Chinese, the name being found in Chinese herbology literature such as ''Daily Use Materia Medica'' () (1329) and ''Compendium of Materia Medica'' () published in 1578.T. Hori, A historical survey of Ginkgo biloba based on Japanese and Chinese classical literatures, Plant Morphology, 2001, 31, 31–40

Despite its spelling, which is due to a complicated etymology including a transcription error, "ginkgo" is usually pronounced , which has given rise to the common alternative spelling "gingko". The spelling pronunciation is also documented in some dictionaries.

Engelbert Kaempfer first introduced the spelling in his book '' Amoenitatum Exoticarum'', taking it from Japanese herbalist in his manuscript, ', acquired in Dejima between 1689–91. It is considered that he may have misspelled or as . This misspelling was included by Carl Linnaeus in his book ''Mantissa plantarum II'' and has become the name of the tree's genus.

Food

In Korea, the seed flesh is eaten with rice.

References

Citations

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External links

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Extant Permian first appearances
Gymnosperm genera
Permian plants
Prehistoric gymnosperm genera
Taxa named by Carl Linnaeus