Academic literature on the topic 'Cycadophytes'

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Journal articles on the topic "Cycadophytes"

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Banerji, J. "Plant fossils from Dubrajpur Formation, Bihar and their significance in stratigraphy." Journal of Palaeosciences 38 (December 31, 1989): 122–30. http://dx.doi.org/10.54991/jop.1989.1646.

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The paper deals with the plant fossils of Dubrajpur Formation exposed at Khatangi Hill in the Rajmahal Basin, Bihar. The assemblage is dominated by cycadophytes, though pteridophytes are quite frequent. Conifers are poorly represented. The genera Onychiopsis, Ctenis, Taeniopteris and Pagiophyllum are recovered for the first time. In view of the present finding, the age of the Khatangi sediments is discussed. The dominance of cycadophytes and poor representation of conifers indicates subtropical to tropical climate prevailing at that time.
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Kustatscher, Evelyn, Giovanni G. Scanu, Jiří Kvaček, and Johanna H. A. Van Konijnenburg-van Cittert. "The Krasser collection In the Faculty of Sciences, Charles University, Prague – New insights into the Middle Jurassic flora of Sardinia." Fossil Imprint 72, no. 3-4 (2016): 140–54. http://dx.doi.org/10.14446/fi.2016.140.

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Revision of part of the Middle Jurassic flora of Sardinia, the Krasser collection, stored in Prague (Lovisato B collection), containing 23 fossil taxa of horsetails, ferns, cycadophytes, ginkgophytes and conifers. The conifers are most diverse, followed by cycadophytes and ferns. The composition of this assemblage differs notably from the Lovisato collection stored in Cagliari, suggesting that it might derive from a different stratigraphic level and/or palaeoenvironment. The palaeodiversity of the Middle Jurassic flora of Sardinia increases to 46 fossil taxa with this revision. Cycadolepis sp. Nilssonia sp., Nilssonia sp. cf. N. orientalis, Pagiophyllum sp. and Agathoxylon sp. are described for the first time from the Middle Jurassic of Sardinia.
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Rajanikanth, A. "Diversification and evolution of Early Cretaceous East Coast flora of India." Journal of Palaeosciences 45 (December 31, 1996): 369–77. http://dx.doi.org/10.54991/jop.1996.1257.

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The Early Cretaceous continental sediments in the East Coast of India are characterized by the Ptilophyllum flora. Interplay of tectonism and sedimentation caused plant fossil preservation in different unconnected paralic deposits distributed in Cauvery, Palar, Krishna-Godavari and Mahanadi basins and in the associated Pranhita-Godavari Graben. Plant megafossils assigned to pteridophytes, pteridosperms, cycadophytes, Taxales, Ginkgoales and Coniferales are variously distributed in these basins. Differential preservation of plant parts denotes an incomplete evolutionary pattern. Variation within the basinal flora reflects a localised aspect. Plant fossils preserved in the Cauvery, Palar, Krishna-Godavari and Mahanadi basins reflect a near shore continental sedimentary fill subjected to more dynamic events like marine transgression, which probably did not allow better preservation of plant fossils. Paucity of carbonised/silicified material, abundance of impressions of plant leaf fossils, scarcity of wood and reproductive parts indicate an unfavourable environment for plant fossil preservation in these pericratonic basins. Whereas in the associated Pranhita-Godavari Graben the plant fossils are better preserved in the sub-aerially exposed basinal areas away from the main coast-line. The Early Cretaceous flora of Cauvery, Palar and Krishna-Godavari basins dominated by cycadophytes suggests presence of seaward margins of fluviodeltaic palaeoenvironment. The pteridophyte dominant flora of Mahanadi Basin represents a decreasing marine influence contrary towards the south-eastwards. The evolution and diversification of the East Coast Early Cretaceous flora runs parallel to other intracratonic basinal flora. The uniformity in the floral component supports an equable climate. Conifers being the upland floral elements constitute chief components of intracratonic basinal flora. The fluviomarginal elements like cycadophytes predominate the pericratonic sedimentation with some upland near basinal taxa. Pteridosperms and Ginkgoales are scanty. Presence of leaves with entire margin indicates a favourable growth environment.
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Le, Renard Ludovic, Christine Strullu-Derrien, Mary Berbee, and Mario Coiro. "A new leaf inhabiting ascomycete from the Jurassic (ca 170 Mya) of Yorkshire, UK, and insights into the appearance and diversification of filamentous Ascomycota." IMA Fungus 15, no. 1 (2024): 34. https://doi.org/10.1186/s43008-024-00162-9.

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Leaf-associated fungi, the fungi that depend on leaves to sporulate, have a rich Cenozoic record, however their earlier diversity is poorly characterized. Here we describe<i>Harristroma eboracense</i>gen. et sp. nov., a Middle Jurassic leaf-associated fungus colonizing the leaf cuticle of<i>Nilssonia tenuicaulis</i>(cycadophyte). To place our newly described species into a picture of the diversification of Mesozoic fungi, we reassess fossils with leaf-associated stromata in the context of fungal molecular phylogeny. Being melanized, with radiate stromata, and on leaves,<i>H. eboracense</i>and other fossils from the Jurassic and earlier periods are probably related to filamentous<i>Ascomycota</i>in the superclass<i>Leotiomyceta.</i>Characters needed for further resolution of leaf-associated fungal biology and classification, such as the presence of an ostiole for spore discharge and appressoria for entry into leaf tissue first appear in the Mesozoic fossil record. Among Early Cretaceous fossils,<i>Spataporthe taylorii</i>represents the oldest unambiguous evidence of perithecial<i>Sordariomycetes</i>while<i>Protographum luttrellii</i>and<i>Bleximothyrium ostiolatum</i>are the oldest<i>Dothideomycetes</i>thyriothecia. Environmental observations show that broad leaved gymnosperms (especially cycadophytes) growing in warm temperate wet forests might have been the first environment for the radiation of<i>Leotiomyceta.</i>
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Pandya, Neeru, and Sukh-Dev. "Fossil flora of Gollapalle Formation." Journal of Palaeosciences 38 (December 31, 1989): 147–54. http://dx.doi.org/10.54991/jop.1989.1648.

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The plant megafossil assemblage of Gollapalle Formation, Andhra Pradesh is enriched and updated. The flora is chiefly constituted of Cladophlebis, Sphenopteris, Marattiopsis, Pachypteris, Taeniopteris, Ptillophyllum, Dictyozamites, Pterophyllum, Williamsonia, Bucklandia, Elatocladus, Pagiophyllum, Brachyphyllum and Araucarites. Conifers and cycadophytes are dominant: pteridophytes and pteridosperms are poorly represented. Early Cretaceous age is supported for the Gollapalle flora.
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Banerji, J., and B. N. Jana. "Early Cretaceous megaflora from Bartala Hill, Rajmahal Basin, India." Journal of Palaeosciences 49, no. (1-3) (2000): 51–56. http://dx.doi.org/10.54991/jop.2000.131.

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The present paper deals with megafloral investigation of Bartala locality of Rajmahal Basin. Nine taxa are recorded for the first time from this locality: Hausmannia, Taeniopteris, Anomozamites, Pterophyllum, Pseudoctenis, Dictyozamites, Ginkgoites, Desmiophyllum. Elatocladus and Brachyphyllum. The assemblage is dominated by cycadophytes, pteridophytes and conifers are scarcely represented. Predominance of Anomozamites in this assemblage perhaps shows the local variation. On the basis of assemblage correlation, an Early Cretaceous age has been suggested.
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Patra, B. P., and N. K. Sahoo. "Some observations on the occurrence of Cycadophytes and Bennettitales in the East Coast Upper Gondwana Athgarh Sandstone, Cuttack and Khurda districts of Orissa, India." Journal of Palaeosciences 44 (December 31, 1995): 139–51. http://dx.doi.org/10.54991/jop.1995.1205.

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Athgarh Sandstone is rich in plant megafossils, in which the pteridophytes and conifers are dominated followed by Bennettitales and Cycadophytes. The species described in this paper are: Ptilophyllum acutifolium, Ptilophyllum spp., Pterophyllum kingianum, Pterophyllum sp. cf. P. distans, Otozamites penna, Otozamites sp. cf. O. kachchhensis, Anomozamites fissus, Dictyozamites sp. and Taeniopteris spatulata. A comparison of this assemblage with similar other assemblages from the Lower Cretaceous of India has also been made.
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Golovneva, L. B. "The Oloy floristic assemblage from the Cretaceous deposits of the Il’guveem river head, Northeastern Russia." Palaeobotany 6 (2015): 68–79. http://dx.doi.org/10.31111/palaeobotany/2015.6.68.

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The Oloy floristic assemblage comes from volcanic-sedimentary deposits of the Teleneut Unit, distributed in the Il’guveem river head, at the Oloy, Great Anuy and Yablon Rivers interfluve area. This area belongs to the Anadyr segment of the Okchotsk-Chukotka volcanic belt (Belyi, 1977). The Oloy floristic assemblage consists of 15 species. Equisetopsida: Equisetum sp. Polypodiopsida: Cladophlebis sp., Coniopteris sp., Tchaunia tchaunensis Samyl. et Philipp. Czekanowskiopsida: Phoenicopsis ex gr. angustifolia Heer. Cycadophytes: Heilungia oloensis Samyl. et Philipp., Taeniopteris sp., Pterophyllum sp. Ginkgoopsida: Ginkgo sp., Sphenobaiera sp. Pinopsida: Pagiophyllum zhuravlevii Golovn., Araucarites sp., Taxodium sp., Sequoia sp., Pityophyllum sp. Among them gymnosperms predominate. Angiosperms are not revealed. Cycadophytes are represented by three genera (Heilungia, Taeniopteris and Pterophyllum). Taxonomic composition of the Oloy floristic assemblage most closely resembles the composition of the Chaun flora, which comes from the Coniacian deposits of the Chaun Group of Central Chukotka. From 15 species of the Oloy assemblage 13 species are common with the Chaun ones (besides Taeniopteris иPterophyllum). Among common taxa there are the characteristic endemic plants of the Chaun flora: Tchaunia tchaunensis and Pagiophyllum zhuravlevii. The great systematic similarity of these floras indicate that they were even-aged and belonged to the single phytogeographic area – the Chukotka subprovince of the Mountain Okchotsk-Chukotka province (Golovneva, 2014b).
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Kustatscher, Evelyn, and Johanna H. A. van Konijnenburg-van Cittert. "Seed ferns and Cycadophytes from the Triassic Flora of Thale (Germany)." Neues Jahrbuch für Geologie und Paläontologie - Abhandlungen 258, no. 2 (2010): 195–217. http://dx.doi.org/10.1127/0077-7749/2010/0097.

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MacLaren, Jamie A., Philip S. L. Anderson, Paul M. Barrett, and Emily J. Rayfield. "Herbivorous dinosaur jaw disparity and its relationship to extrinsic evolutionary drivers." Paleobiology 43, no. 1 (2016): 15–33. http://dx.doi.org/10.1017/pab.2016.31.

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AbstractMorphological responses of nonmammalian herbivores to external ecological drivers have not been quantified over extended timescales. Herbivorous nonavian dinosaurs are an ideal group to test for such responses, because they dominated terrestrial ecosystems for more than 155 Myr and included the largest herbivores that ever existed. The radiation of dinosaurs was punctuated by several ecologically important events, including extinctions at the Triassic/Jurassic (Tr/J) and Jurassic/Cretaceous (J/K) boundaries, the decline of cycadophytes, and the origin of angiosperms, all of which may have had profound consequences for herbivore communities. Here we present the first analysis of morphological and biomechanical disparity for sauropodomorph and ornithischian dinosaurs in order to investigate patterns of jaw shape and function through time. We find that morphological and biomechanical mandibular disparity are decoupled: mandibular shape disparity follows taxonomic diversity, with a steady increase through the Mesozoic. By contrast, biomechanical disparity builds to a peak in the Late Jurassic that corresponds to increased functional variation among sauropods. The reduction in biomechanical disparity following this peak coincides with the J/K extinction, the associated loss of sauropod and stegosaur diversity, and the decline of cycadophytes. We find no specific correspondence between biomechanical disparity and the proliferation of angiosperms. Continual ecological and functional replacement of pre-existing taxa accounts for disparity patterns through much of the Cretaceous, with the exception of several unique groups, such as psittacosaurids that are never replaced in their biomechanical or morphological profiles.
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Book chapters on the topic "Cycadophytes"

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Delevoryas, T. "Comments on the Role of Cycadophytes in Antarctic Fossil Floras." In Antarctic Paleobiology. Springer New York, 1990. http://dx.doi.org/10.1007/978-1-4612-3238-4_13.

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TAYLOR, T. "Cycadophytes." In Biology and Evolution of Fossil Plants. Elsevier, 2009. http://dx.doi.org/10.1016/b978-0-12-373972-8.00017-6.

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"6. The Fossil Cycadophytes." In The Biology of the Cycads. Cornell University Press, 2020. http://dx.doi.org/10.7591/9781501737329-007.

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"CYCADOPHYTA." In Flora of the Sydney Region, 5th ed. Sydney University Press, 2009. http://dx.doi.org/10.2307/j.ctv1wmz4n6.12.

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"CYCADOPHYTA." In Flora of the Sydney Region, 5th ed. Sydney University Press, 2009. http://dx.doi.org/10.2307/j.ctv1wmz4n6.14.

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Renner, Susanne. "Gymnosperms." In The Timetree of Life. Oxford University PressOxford, 2009. http://dx.doi.org/10.1093/oso/9780199535033.003.0015.

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Abstract Gymnosperms, also called Acrogymnospermae (1), are a group of seed-bearing plants (spermatophytes) with ovules on the edge or blade of an open sporophyll or ovuliferous scale (Fig. 1). 7eir closest extant relatives are the angiosperms, which have ovules enclosed in a carpel. Gymnospermae is a problematic name because, when fossils are included as is usually the case, the name is widely understood to apply to a paraphyletic group of seed plants from which the angiosperms also arose (1). 7ere are just over a 1000 living species of gymnosperms in the taxa Cycadophyta, Ginkgophyta, Coniferophyta, and Gnetophyta. Here, the relationships and divergence times of families in these phyla are reviewed.
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