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Dicroidium

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Dicroidium
Temporal range: Late Permian–Sinemurian
Dicroidium odontopteroides fossil leaf, Late Triassic Molteno Formation near Birds River South Africa.
Scientific classification Edit this classification
Kingdom: Plantae
Clade: Tracheophytes
Order: †Corystospermales
Family: †Corystospermaceae
Genus: †Dicroidium
Gothan (1912)
Species
  • Dicroidium crassinervis Australia, Antarctica, South Africa
  • Dicroidium coriaceum, Australia, Antarctica, South Africa
  • Dicroidium dubium Australia, Antarctica, South Africa
  • Dicroidium odontopteroides, Australia, New Zealand, Antarctica, India, South Africa, Argentina, Brazil[1]
  • Dicroidium stelznerianum, Australia, New Zealand, Antarctica, South Africa, Argentina[2]
Synonyms
  • Johnstonia Walkom
  • Harringtonia Frenguelli
  • Dicroidiopsis Frenguelli
  • Diplasiophyllum Frenguelli
  • Zuberia Frenguelli
  • Xylopteris Frenguelli
  • Tetraptilon Frenguelli
  • Hoegia Townrow
  • Jordaniopteris Anderson

Dicroidium is an extinct genus of fork-leaved seed plants. It is the archetypal genus of the corystosperms, an extinct group of seed plants, often called "seed ferns", assigned to the order Corystospermales or Umkomasiales. Species of Dicroidium were widely distributed and dominant over Gondwana during the Triassic (252 to 201 million years ago). Their fossils are known from South Africa, the Arabian Peninsula, Australia, New Zealand, South America, Madagascar, the Indian subcontinent and Antarctica.

Description

Dicroidium zuberi

Within the form genus classification system used in paleobotany, the genus Dicroidium refers specifically to the leaves. Some authors have suggested dividing Dicroidium up into several genera, including Dicroidiopsis, Diplasiophyllum, Zuberia, Xylopteris, Johnstonia and Tetraptilon, but this is rejected by other authors.[4] The leaves of Dicroidium bifurcate (fork) at their base, which is characteristic of all species. The leaves are highly variable in size and morphology, ranging from simple to tripinnate, with the individual leaflets having varying morphologies, including dissected, lobed, needle-like and entire.[5] Some leaf specimens have more than one type of leaflet morphology, which may have been the result of hybridisation between different species.[4] The venation of the leaves is also highly variable, encompassing taeniopteroid, odontopteroid, alethopteroid and simple morphologies.[5]

Whole plant

Reconstruction of the whole plant of Dicroidium odontopteroides , including Umkomasia macleanii (L-P) and Pteruchus africanus (H-K)

Dicroidium plants grew as medium-large sized trees,[5] with some preserved trunk sections 10 metres (33 ft) tall and over 50 centimetres (20 in) wide,[4] with the wood assigned to the genera Kykloxylon and Rhexoxylon. The ovulate reproductive structures are usually assigned to the genus Umkomasia, while the pollen-producing organs are assigned to the genus Pteruchus, with pollen attributable to the genus Falcisporites. These structures are almost never found in organic connection, and their placement as part of the same plant primarily relies on their repeated co-occurrence with each other, and the similarities in the morphology of their cuticles.[6] The leaves grew on short protuberances attached to the stem in a similar way to living Ginkgo biloba.[7][8] The leaves of Dicroidium are suggested to have been deciduous, and shed along with the reproductive organs during the winter. The seeds and pollen are suggested to have been wind dispersed.[4]

Possible whole plant associations include:

Evolution

The earliest Dicroidium species are known from the Late Permian aged Umm Irna Formation of Jordan, which inhabited equatorial humid tropical environments,[6] as well as equivalently aged more southerly subtropical deposits on Indian subcontinent.[11] Following the end-Permian mass extinction, Dicroidium expanded its range southwards across Gondwana, including South Africa, Antarctica, Australia, New Zealand, India and South America,[6] with a record also reported from the Middle Triassic of China.[12] Later Triassic Dicroidum-bearing plants were dominant large canopy forming trees in temperate wetland and forested habitats at mid-high latitudes, extending to the South Pole.[4][5][6] Dicroidium-dominanted ecosystems in Gondwana collapsed during the end-Triassic mass extinction, with Dicroidium surviving in parts of East Antarctica into the Early Jurassic (Sinemurian).[5]

References

  1. ^ THE TRIASSIC TAPHOFLORA FROM PARANA BASIN, SOUTHERN BRAZIL
  2. ^ Retallack G.J. (1985). "Triassic fossil plant fragments from marine rocks of the Murihiku Supergroup, New Zealand". Journal of the Royal Society of New Zealand. 15: 1–26. doi:10.1080/03036758.1985.10421741.
  3. ^ Passo das Tropas, Santa Maria, RS Marco bioestratigráfico triássico na evolução paleoflorística do Gondwana na Bacia do Paraná.
  4. ^ a b c d e Mays, Chris; McLoughlin, Stephen (2020-02-25). "Caught between two mass extinctions: The rise and fall of Dicroidium". Deposits Mag. Retrieved 2023-09-23.
  5. ^ a b c d e Bomfleur, Benjamin; Blomenkemper, Patrick; Kerp, Hans; McLoughlin, Stephen (2018), "Polar Regions of the Mesozoic–Paleogene Greenhouse World as Refugia for Relict Plant Groups", Transformative Paleobotany, Elsevier, pp. 593–611, doi:10.1016/b978-0-12-813012-4.00024-3, ISBN 978-0-12-813012-4, retrieved 2020-11-12
  6. ^ a b c d Blomenkemper, Patrick; Kerp, Hans; Abu Hamad, Abdalla; Bomfleur, Benjamin (July 2020). "Contributions towards whole-plant reconstructions of Dicroidium plants (Umkomasiaceae) from the Permian of Jordan". Review of Palaeobotany and Palynology. 278: 104210. doi:10.1016/j.revpalbo.2020.104210.
  7. ^ Anderson, H.M., Holmes, W.B.K. & Fitness, F.A., 2008. Stems with attached Dicroidium leaves from the Ipswich Coal Measures, Queensland, Australia. Memoirs of the Queensland Museum 52, 1–12.
  8. ^ Anderson, Heidi M.; Barbacka, Maria; Bamford, Marion K.; Holmes, W. B. Keith; Anderson, John M. (2020-01-02). "Dicroidium (foliage) and affiliated wood Part 3 of a reassessment of Gondwana Triassic plant genera and a reclassification of some previously attributed". Alcheringa: An Australasian Journal of Palaeontology. 44 (1): 64–92. doi:10.1080/03115518.2019.1622779. ISSN 0311-5518.
  9. ^ Retallack, G.J.; Dilcher, D.L. (1988). "Reconstructions of selected seed ferns". Missouri Botanical Garden Annals. 75 (3): 1010–1057. doi:10.2307/2399379. JSTOR 2399379.
  10. ^ Retallack G.J. (1977). "Reconstructing Triassic vegetation of southeastern Australia: a new approach to the biostratigraphy of Gondwanaland". Alcheringa. 1: 247–265. doi:10.1080/03115517708527763.
  11. ^ Schneebeli-Hermann, Elke; Kürschner, Wolfram M.; Kerp, Hans; Bomfleur, Benjamin; Hochuli, Peter A.; Bucher, Hugo; Ware, David; Roohi, Ghazala (April 2015). "Vegetation history across the Permian–Triassic boundary in Pakistan (Amb section, Salt Range)". Gondwana Research. 27 (3): 911–924. doi:10.1016/j.gr.2013.11.007.
  12. ^ Sun, Yanqi; Deng, Shenghui; Lu, Yuanzheng; Fan, Ru; Ma, Xueying; Lyu, Dan (June 2024). "The first record of the Gondwanan seed fern Dicroidium Gothan in Laurasia". Review of Palaeobotany and Palynology. 325: 105114. doi:10.1016/j.revpalbo.2024.105114.
  • Bomfleur, B. and Kerp, H. (2010). Dicroidium diversity in the Upper Triassic of north Victoria Land, East Antarctica.
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