Caytonia Temporal range: − | |
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Caytonia nathorstii ovulate structure, Middle Jurassic, Gristhorpe Bed, Cloughton Formation, Cayton Bay, Yorkshire. | |
Scientific classification | |
Kingdom: | Plantae |
Clade: | Tracheophytes |
Division: | † Pteridospermatophyta |
Order: | † Caytoniales |
Family: | † Caytoniaceae |
Genus: | † Caytonia H.H.Thomas, 1925 |
Species | |
Caytonia is an extinct genus of seed ferns.
Caytonia has berry-like cupules with numerous small seeds arrayed along axes [2]
Different organs attributed to the same original plant can be reconstructed from co-occurrence at the same locality and from similarities in the stomatal apparatus and other anatomical peculiarities of fossilized cuticles.
A gametophyte is one of the two alternating multicellular phases in the life cycles of plants and algae. It is a haploid multicellular organism that develops from a haploid spore that has one set of chromosomes. The gametophyte is the sexual phase in the life cycle of plants and algae. It develops sex organs that produce gametes, haploid sex cells that participate in fertilization to form a diploid zygote which has a double set of chromosomes. Cell division of the zygote results in a new diploid multicellular organism, the second stage in the life cycle known as the sporophyte. The sporophyte can produce haploid spores by meiosis that on germination produce a new generation of gametophytes.
The Embryophyta, or land plants, are the most familiar group of green plants that comprise vegetation on Earth. Embryophytes have a common ancestor with green algae, having emerged within the Phragmoplastophyta clade of green algae as sister of the Zygnematophyceae. The Embryophyta consist of the bryophytes plus the polysporangiophytes. Living embryophytes therefore include hornworts, liverworts, mosses, lycophytes, ferns, gymnosperms and flowering plants. The land plants have diplobiontic life cycles and it is accepted now that they emerged from freshwater, multi-celled algae.
A sporophyte is the diploid multicellular stage in the life cycle of a plant or alga which produces asexual spores. This stage alternates with a multicellular haploid gametophyte phase.
The term Pteridospermatophyta is a polyphyletic wastebasket taxon of extinct seed-bearing plants (spermatophytes). The earliest fossil evidence for plants of this type is the genus Elkinsia and the Lyginopterids of late Devonian age. They flourished particularly during the Carboniferous and Permian periods. Pteridosperms declined during the Mesozoic Era and had mostly disappeared by the end of the Cretaceous Period, though some pteridosperm-like plants seem to have survived into Eocene times, based on fossil finds in Tasmania.
Plant reproduction is the production of new offspring in plants, which can be accomplished by sexual or asexual reproduction. Sexual reproduction produces offspring by the fusion of gametes, resulting in offspring genetically different from either parent. Asexual reproduction produces new individuals without the fusion of gametes, resulting in clonal plants that are genetically identical to the parent plant and each other, unless mutations occur.
The Caytoniales are an extinct order of seed plants known from fossils collected throughout the Mesozoic Era, around 252 to 66 million years ago. They are regarded as seed ferns because they are seed-bearing plants with fern-like leaves. Although at one time considered angiosperms because of their berry-like cupules, that hypothesis was later disproven. Nevertheless, some authorities consider them likely ancestors or close relatives of angiosperms. The origin of angiosperms remains unclear, and they cannot be linked with any known seed plants groups with certainty.
Sagenopteris is a genus of extinct seed ferns from the Triassic to late Early Cretaceous.
Caytonanthus is an extinct genus of seed ferns.
A spermatophyte, also known as phanerogam or phaenogam, is any plant that produces seeds, hence the alternative name seed plant. Spermatophytes are a subset of the embryophytes or land plants. They include most familiar types of plants, including all flowering plants and gymnosperms, but exclude some other types of plants such as ferns, mosses, and algae.
Dicroidium is an extinct genus of fork-leaved seed plants assigned to the order Umkomasiales (corystosperms) that were widely distributed over Gondwana during the Triassic. Their fossils are known from South Africa, the Arabian Peninsula, Australia, New Zealand, South America, Madagascar, the Indian subcontinent and Antarctica. They were first discovered in Triassic sediments of Tasmania by Morris in 1845. Fossils from the Umm Irna Formation in Jordan and in Pakistan indicate that these plants already existed in Late Permian. Late surviving members of the genus are known from the Early Jurassic (Sinemurian) of East Antarctica. Within paleobotany, Dicroidium is a form genus used to refers to the leaves, associated with ovuluate organs classified as Umkomasia and pollen organs classified as Pteruchus, while Dicroidum is also used collectively to refer to the whole plant.
Lepidopteris is a form genus for leaves of Late Permian to Early Jurassic Peltaspermaceae, an extinct family of seed plants, which lived from around 260 to 190 million years ago in what is now Australia, Antarctica, India, South America, South Africa, Russia and China. Nine species are currently recognized. Lepidopteris was a common and widespread seed fern, which survived the Permian-Triassic extinction event but succumbed to the Triassic-Jurassic extinction event. Lepidopteris callipteroides is especially common between the first two episodes of Permian-Triassic extinction event, and L. ottonis forms a comparable acme zone immediate before the Triassic-Jurassic extinction event. Lepidopteris would persist into the Early Jurassic in Patagonia, represented by the species Lepidopteris scassoi.
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.
Umkomasia macleanii is an ovulate structure of a seed fern (Pteridospermatophyta and the nominate genus of Family Umkomasiaceae. It was first described by Hamshaw Thomas from the Umkomaas locality of South Africa.
Pteruchus africanus is a pollen organ of a seed fern (Pteridospermatophyta). It was first described by Hamshaw Thomas from the Umkomaas locality of South Africa.
Pteruchus is a form genus for pollen organs of the seed fern (Pteridospermatophyta family Umkomasiaceae. It was first described by Hamshaw Thomas from the Umkomaas locality of South Africa. It is associated with the seed bearing organs Umkomasia and Dicroidium leaves.
Moresnetiaceae is a natural family of seed ferns in the Division Pteridospermatophyta that appears in the North American and European Devonian to Carboniferous coal measures.
Caytonia nathorstii is an extinct species of seed ferns.
Sagenopteris phillipsii are leaves of extinct species of seed ferns.
Dictyopteridiaceae are an extinct family of glossopterid plants known from the Permian period.
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, that were widespread over Gondwana during the Middle and Late Triassic. Other fossil Mesozoic seed plants with similar 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. Their oldest records date to the Late Permian from the Umm Irna Formation of Jordan, as well as Pakistan. Late surviving Dicroidium-bearing corystosperms are known from the Early Jurassic (Sinemurian) of East Antarctica. A potential corystosperm sensu lato, the leaf fossil Komlopteris cenozoicus, is known from the Eocene of Tasmania, at least 13 million years after the Cretaceous–Paleogene extinction event.