Williamsonia Temporal range: | |
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Cross section of Williamsonia harrisiana (India, Jurassic - Early Cretaceous) | |
Scientific classification | |
Kingdom: | Plantae |
Clade: | Tracheophytes |
Clade: | Gymnosperms |
Order: | † Bennettitales |
Family: | † Williamsoniaceae |
Genus: | † Williamsonia Carruth., 1870 [1] |
Type species | |
Williamsonia gigas Carruth., 1870 [1] |
Williamsonia is a genus of plant belonging to Bennettitales, an extinct order of seed plants. Within the form classification system used in paleobotany, Williamsonia is used to refer to female seed cones, which are associated with plants that also bore the male flower-like reproductive structure Weltrichia. [2]
The monosporiangiate [2] female Williamsonia seed cone (sometimes described as a "flower" though this does not imply homology with angiosperm flowers [3] ) consists of an ovulate receptacle enclosed by bracts (modified leaves), with the receptacle bearing sporophylls with terminal seeds/ovules, which are surrounded by interseminal scales. [4] The micropyle of the ovules varied from protruding above the cone to slightly sunken in, depending on the species. [2] The cones were of variable shape, with reported morphologies including pyriform (pear shaped), ovoid, subspheroidal, and oblate spheroid [2] and could be up to 15 centimetres (5.9 in) in diameter. As many as 25–50 ovules could be present in each cone. [5] The cone was borne on a peduncle, and grew at the apex of a branch. [6] [2] In at least some species, only one Williamsonia cone grew per active branch at any one time/season, while the cones from the preceding season/time developed into mature seed cones. [6] The cones have been suggested to be wind pollinated. [7] In at least some species, the cones increased in size during maturation, which might reflect the transformation of the interseminal scales into a fleshy coating possibly used to attract seed dispersers. [6]
Williamsonia is typically associated with the male flower-like reproductive structure Weltrichia. It is unclear whether the parent plants were monoecious (having both structures on one plant) or dioecious (where each plant only has one gender of reproductive organ). In Kimuriella densifolia from the Late Jurassic of Japan and Williamsonia gigas from the Middle Jurassic of England, the Williamsonia cone is associates with leaves assignable to the genus Zamites, [6] while Williamsonia carolinensis from the Late Triassic of North America is associated with leaves assigned to Eoginkgoites . [8] Kimuriella is thought to have been a divaricately branching, low growing shrub with a maximum height of 2–3 metres, with a growth form similar to that of Wielandiella , while Williamsonia gigas may have been more cycad-like. In Kimuriella and W. gigas, the axes (assigned to Bucklandia in W. gigas), which were up to 16 millimetres (0.63 in) and 40–50 millimetres (1.6–2.0 in) wide respectively, were densely covered with persistent leaf bases, which were apparently sloughed off in older branches. [6] The affinity of the cycad-like Williamsonia sewardiana from Early Cretaceous Rajmahal Hills of India [9] to the family Williamsoniaceae has been questioned, with some scholars suggesting that the species may represent an early species of Cycadeoidaceae instead. [10]
Williamsonia was originally described as Zamia gigas by William Crawford Williamson. [11] William Carruthers proposed the name Williamsonia in 1870, with the type species being W. gigas from the Middle Jurassic of England. [1] When originally specifying the genus, Carruthers specifically referred to the foliage, which modern authors usually assign to the foliage genus Zamites. However, later authors beginning with Tom Harris's 1969 publication The Yorkshire Jurassic Flora used Williamsonia to refer to the ovulate reproductive organs. [3]
Fossils of Williamsonia are known spanning from the Middle Triassic [3] to Late Cretaceous, [7] and have been found worldwide, including in Europe, [12] Australia, [3] North America, [8] [7] East Asia [6] India [13] and South America. [14]
Araucariaceae – also known as araucarians – is a family of coniferous trees. The family achieved its maximum diversity during the Jurassic and Cretaceous periods, when it was distributed almost worldwide. Most of the Araucariaceae in the Northern Hemisphere vanished in the Cretaceous–Paleogene extinction event, and they are now largely confined to the Southern Hemisphere, except for a few species of Agathis in Southeast Asia.
Gnetophyta is a division of plants, grouped within the gymnosperms, that consists of some 70 species across the three relict genera: Gnetum, Welwitschia, and Ephedra. Fossilized pollen attributed to a close relative of Ephedra has been dated as far back as the Early Cretaceous. Though diverse in the Early Cretaceous, only three families, each containing a single genus, are still alive today. The primary difference between gnetophytes and other gymnosperms is the presence of vessel elements, a system of small tubes (xylem) that transport water within the plant, similar to those found in flowering plants. Because of this, gnetophytes were once thought to be the closest gymnosperm relatives to flowering plants, but more recent molecular studies have brought this hypothesis into question, with many recent phylogenies finding them to be nested within the conifers.
The Pinaceae, or pine family, are conifer trees or shrubs, including many of the well-known conifers of commercial importance such as cedars, firs, hemlocks, piñons, larches, pines and spruces. The family is included in the order Pinales, formerly known as Coniferales. Pinaceae are supported as monophyletic by their protein-type sieve cell plastids, pattern of proembryogeny, and lack of bioflavonoids. They are the largest extant conifer family in species diversity, with between 220 and 250 species in 11 genera, and the second-largest in geographical range, found in most of the Northern Hemisphere, with the majority of the species in temperate climates, but ranging from subarctic to tropical. The family often forms the dominant component of boreal, coastal, and montane forests. One species, Pinus merkusii, grows just south of the equator in Southeast Asia. Major centres of diversity are found in the mountains of southwest China, Mexico, central Japan, and California.
Bennettitales is an extinct order of seed plants that first appeared in the Permian period and became extinct in most areas toward the end of the Cretaceous. Bennettitales were amongst the most common seed plants of the Mesozoic, and had morphologies including shrub and cycad-like forms. The foliage of bennettitaleans is superficially nearly indistinguishable from that of cycads, but they are distinguished from cycads by their more complex flower-like reproductive organs, at least some of which were likely pollinated by insects.
Cycadeoidea is an extinct genus of bennettitalean plants known from the Cretaceous of North America, Europe and Asia. They grew as cycad-like plants with a short trunk topped with a crown of leaves.
Brachyphyllum is a form genus of fossil coniferous plant foliage. Plants of the genus have been variously assigned to several different conifer groups including Araucariaceae and Cheirolepidiaceae. They are known from around the globe from the Late Carboniferous to the Late Cretaceous periods. B. sattlerae was named after the fictional palaebotanist Ellie Sattler from the Jurassic Park franchise.
Zamites is a genus of sterile foliage known from the Mesozoic of North America, Europe, India and Antarctica through the Eocene of North America. It was erected as a form taxon for leaves that superficially resembled the extant cycad Zamia, however it is now believed to belong to a similar but phylogenetically different group, the cyacadeoids (Bennettitales). The fronds are linear or lanceolate in shape, and pinnately compound, with pinnae with parallel veins and smooth margins, and symmetrical and constricted at the base where they are attached obliquely to the upper surface of the rachis. It has been interpreted as a Bennettitalean plant in the family Williamsoniaceae. It is associated with the ovulate cone Williamsonia and male cone Weltricihia.
This article records new taxa of fossil plants that are scheduled to be described during the year 2015, as well as other significant discoveries and events related to paleobotany that are scheduled to occur in the year 2015.
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Umkomasia is a genus of seed bearing organs produced by corystosperm seed ferns, first based on fossils collected by Hamshaw Thomas from the Burnera Waterfall locality near the Umkomaas River of South Africa. He recognized on the basis of cuticular similarities that the same plant produced pollen organs Pteruchus and the leaves Dicroidium. Various other corystosperm seed bearing organs from the Jurassic and Cretaceous have been assigned to this genus, but recently have been given distinct genera, with Umkomasia being restricted to the Triassic.
Corystosperms are a group of extinct seed plants belonging to the family Corystospermaceae assigned to the order Corystospermales or Umkomasiales. They were first described based on fossils collected by Hamshaw Thomas from the Burnera Waterfall locality near the Umkomaas River of South Africa. Corystosperms are typified by a group of plants that bore forked Dicroidium leaves, Umkomasia cupulate ovulate structures and Pteruchus pollen organs, which grew as trees that were widespread over Gondwana during the Middle and Late Triassic. Other fossil Mesozoic seed plants with similar leaf and/or reproductive structures have also sometimes been included within the "corystosperm" concept sensu lato, such as the "doyleoids" from the Early Cretaceous of North America and Asia. A potential corystosperm sensu lato, the leaf genus Komlopteris, is known from the Eocene of Tasmania, around 53-50 million years old, over 10 million years after the Cretaceous–Paleogene extinction event.
This article records new taxa of plants that are scheduled to be described during the year 2018, as well as other significant discoveries and events related to paleobotany that occurred in the year 2018.
This list of 2013 in paleobotany records new fossil plant taxa that were described during 2013, as well as other significant discoveries and events related to paleobotany that occurred in the year.
Nilssoniopteris is an extinct form genus of leaves belonging to the Bennettitales. Leaves are slender and often entire-margined (smooth-edged), though some species have dissected leaves with numerous small segments extending down to the rachis of the leaf. Nilssoniopteris-like leaves are distinguished by their syndetocheilic stomata, indicating bennettitalean affinities. Similar "taeniopterid" leaves are placed in the genus Nilssonia if their stomata are instead haplocheilic, or Taeniopteris if the cuticle is not preserved. Leaves of Nilssoniopteris vittata from the Middle Jurassic of England are associated with bisexual Williamsoniella reproductive structures.
This paleobotany list records new fossil plant taxa that were to be described during the year 2012, as well as notes other significant paleobotany discoveries and events which occurred during 2012.
Eoginkgoites is an extinct form genus of bennettitalean leaves from the Late Triassic of North America. Despite its palmate (hand-shaped) appearance similar to some early ginkgo species, it belongs to a different gymnosperm order, the Bennettitales. The leaf is deeply segmented into five to seven narrow, club-shaped lobes which twist around a very short rhachis. This leads to an overall fan-shaped leaf situated at the end of a long petiole. The leaf has paracytic stomata and veins which strongly branch and lead to a marginal vein at the edge of each leaflet. These structural traits are all shared with benettitaleans. Williamsonia carolinensis, an ovule-bearing bennettitalean cone, has been found closely associated with Eoginkgoites leaves, seemingly confirming its benettitalean identity.
This paleobotany list records new fossil plant taxa that were to be described during the year 2023, as well as notes other significant paleobotany discoveries and events which occurred during 2023.
Pararaucaria is a genus of conifer cone belonging to the extinct family Cheirolepidiaceae. Fossils are known from the Lower Jurassic to Early Cretaceous of North America, Europe, South America and Asia. It is associated with Brachyphyllum-type foliage.
Weltrichia is a genus belonging to the extinct seed plant group Bennettitales. It is a form genus representing flower-like male pollen-producing organs. It is associated with the female ovulate cone Williamsonia.
Wielandiella is an extinct genus of bennettitalean shrub known from the Late Triassic (Rhaetian) of Europe and Greenland, and the Middle Jurassic of China.