This paleobotany list records new fossilplanttaxa that were to be described during the year 2023, as well as notes other significant paleobotany discoveries and events which occurred during 2023.
Originally described as a green alga belonging to the group Dasycladales and the family Triploporellaceae; subsequently argued by LoDuca (2024) to be a member of Bryopsidales.[10] Genus includes new species V. dryganti.
Yang et al. (2023) reinterpret Protomelission as an early dasycladalean green alga;[12] however, Xiang et al. (2023) subsequently interpret Protomelission as a scleritome of Cambroclavus, which in turn is considered by the authors to be a probable epitheliozoan-gradeeumetazoan like the contemporaneous chancelloriids, unrelated to bryozoans or to dasycladalean algae.[13]
A herbaceous lycophyte. Genus includes new species T. serratus also includes Lycopodites elongatus Goldenberg (1855).
Lycophyte research
A study on the ground-level trunk vasculature of Sigillaria approximata from the Pennsylvanian Calhoun Coal of Illinois (United States) is published by D'Antonio (2023), who finds evidence indicating that wood growth at the base of the trunk was different from the arborescent lycopsid wood growth model of Cichan (1985).[17][18]
Turner et al. (2023) report diverse phyllotaxis in leaves of the lycopod Asteroxylon mackiei from the Devonian Rhynie chert (United Kingdom), including whorls and spirals, and interpret this finding as suggesting that Fibonacci-style patterning was not ancestral to living land plants, as well as indicative of developmental similarities between lycophyte leaves and reproductive structures.[19]
A fern of uncertain affinities. Originally described as a dennstaedtiaceous fern, but this classification was contested by Zhang (2024).[29] Published online in 2022, but the issue date of the article naming it is listed as March 2023.
A member of the family Hymenophyllaceae, a species of Trichomanessensu lato. Moved from Hymenophyllites angustus Li & Wang (2022).
Pteridological research
A study on fossils of Pecopteris from the Mazon Creek fossil beds (Illinois, United States), indicative of association of a suite of saturated phytohopanoid and aromatised terpenoid diagenetic biomarker products with true fern fossils, is published by Tripp et al. (2023).[35]
Blanco-Moreno & Buscalioni (2023) identify Sphenopteris wonnacottii as a junior synonym of Coniopteris laciniata, provide whole plant reconstruction of C. laciniata, and interpret the variability of the pinnules of C. laciniata as likely caused by the submersion of the apical part of fronds in water during their development.[36]
A conifer with affinities with the family Cupressaceae. The type species is A. pilosum. Published online in 2024, but the issue date is listed as December 2023.
A conifer stem of uncertain affinities. The type species is Y. elegans.
Conifer research
Trümper et al. (2023) report the discovery of fossil trees from the Athesian Volcanic Group (Italy) interpreted as remains of a Permian (Kungurian) forest where conifers were the major arborescent plants, substantiating the presence of coniferopsids in wetlands around the Carboniferous/Permian boundary.[63]
Slodownik et al. (2023) describe new fossil material (including the first putative female reproductive remains) of Araucarioides linearis from the Eocene Macquarie Harbour Formation (Australia), interpret Araucarioides sinuosa to be a junior synonym of A. linearis, and consider A. linearis to be a non-Agathis agathioid belonging to an extinct lineage that originated in the Cretaceous, lived in high paleolatitudes and had adaptations to seasonal environments which allowed it to survive the Cretaceous–Paleogene extinction event.[64]
Andruchow-Colombo et al. (2023) review the fossil record of Podocarpaceae, and argue that the earliest reliable occurrences of members of this family are from the Jurassic of both hemispheres.[65]
A member of the family Trochodendraceae. Moved from Populus retusa Heer (1876).
Basal eudicot research
Evidence from the palynomorph fossil record, interpreted as indicating that members of the family Proteaceae reached South African Cape in the Late Cretaceous from North-Central Africa rather than from Australia across the Indian Ocean, is presented by Lamont, He & Cowling (2023).[76]
Rosid clade fruits of uncertain affinities. The type species is F. aligeri.
Superrosid research
Nishino et al. (2023) study the composition of a fossil forest from the Miocene Nakamura Formation of the Mizunami Group (Japan), including stumps of Wataria parvipora and leaves of Byttneriophyllum tiliifolium, and interpret their finding as suggesting that W. parvipora and B. tiliifolium were parts of the same plant, as well as suggesting that Byttneriophyllum-bearing plants might have belonged to the subfamily Helicteroideae.[123]
Fossil wood with anatomical features found in diverse extant flowering plant groups, might be placed at the base of the asterids, close to Malpighiales, close to Proteales at the base of eudicots, or even in Laurales. The type species is C. paleocenicum.
Flower of uncertain affinities, possibly related to members of the family Apiaceae belonging to the tribe Saniculeae or to the subtribe Scandicinae within the tribe Scandiceae. The type species is Q. kishenehnensis.
An early angiosperm of uncertain phylogenetic placement, most closely related to magnoliids, possibly with lauralean affinities. The type species is R. virginiensis.
An early angiosperm of uncertain affinities. The type species is X. shengliensis.
A study on the affinities of Santaniella, based on data from new fossil material from the Lower Cretaceous Crato Formation (Brazil), is published by Pessoa et al. (2023), who don't support the interpretation of Santaniella as a ranuculid, and consider it to be a mesangiosperm of uncertain affinities, possibly a magnoliid.[132]
Pessoa, Ribeiro & Christenhusz (2023) describe new fossil material of Araripia florifera from the Early Cretaceous of Brazil, interpret its anatomy as indicating that it did not belong to the family Calycanthaceae, and assign it to the new family Araripiaceae in the stem group of Laurales.[133]
Angiosperm research
A study aiming to determine the affinities of 24 exceptionally preserved fossil flowers is published by López-Martínez et al. (2023).[134]
A study aiming to determine the phylogenetic relationships of nine putative magnolialean fossils is published by Doyle & Endress (2023).[135]
Chambers & Poinar (2023) reinterpret Endobeuthos paleosum as a member of the family Proteaceae;[136] this interpretation is subsequently contested by Lamont & Ladd (2024).[137]
A study on the diversification of the flowering plant throughout their evolutionary history is published by Thompson & Ramírez-Barahona (2023), who report evidence of stable extinction rates through time and find no evidence of a significant impact of the Cretaceous–Paleogene extinction event on the extinction rates of major flowering plant lineages.[138]
A study on the anatomy and affinities of Tingia unita, based on data from specimens from the Permian Taiyuan Formation (China), is published by Yang, Wang & Wang (2023), who confirm that T. unita was a progymnosperm belonging to the group Noeggerathiales.[171]
A study on the phylogenetic relationships and evolutionary history of cycads, based on data from extant and fossil taxa, is published by Coiro et al. (2023).[172]
Evidence from nitrogen isotopic measurements from fossilized cycad leaves and ancestral state reconstructions, interpreted as indicating that symbiosis of with N2-fixing cyanobacteria wasn't ancestral within cycads but rather arose independently in the lineages leading to living cycads during or after the Jurassic, is published by Kipp et al. (2023).[173]
Fu et al. (2023) report the presence of ovules enclosed within the ovaries of specimens of Nanjinganthus dendrostyla, and consider their findings to be consistent with the interpretation of Nanjinganthus as an Early Jurassic angiosperm.[174]
Vajda et al. (2023) interpret Ricciisporites tuberculatus as an aberrant pollen produced by Lepidopteris ottonis plants, and interpret its fossil record as indicative of the competitive success of plants which adopted the asexual reproductive strategy under stressed environmental conditions before and during the Triassic–Jurassic extinction event;[184] their interpretation of Ricciisporites and Cycadopites as produced by the same plant is subsequently contested by Zavialova (2024)[185] and reaffirmed by Vajda et al. (2024).[186]
A study on the vegetation in Central Africa from the middle Aptian to early Albian, as indicated by palynomorphs from the Doseo Basin in the Central African Rift system, is published by Dou et al. (2023), who identify two assemblages of spore and pollen fossils, and interpret the differences between the assemblages as indicative of a vegetation change related to change from relatively arid to humid climate.[187]
Malaikanok et al. (2023) describe fossil pollen grains of members of the family Fagaceae from the Oligocene to Miocene Ban Pa Kha Subbasin of the Li Basin (Thailand), and interpret the studied fossils as indicating that, contrary to previous interpretations of the palynological record, tropical Fagaceae-dominated forests existed in northern Thailand at least since the late Paleogene and persisted into the modern vegetation of Thailand.[188]
A study on the environmental changes in the Lake Baikal region during the Marine Isotope Stage 3, as indicated by palynological data, is published by Shichi et al. (2023), who find that the dispersal of Homo sapiens into Baikal Siberia coincided with climate changes resulting in warm and humid conditions and vegetation changes.[189]
Evidence from the study of Last Interglacial pollen records across Europe, interpreted as indicating that European forests before the arrival of Homo sapiens included substantial open and light woodland elements, is presented by Pearce et al. (2023).[190]
Research
A study on the evolution of the phenotypic disparity of plants, based on data from extant and fossil taxa, is published by Clark et al. (2023), who find that the morphological distinctiveness of extant plant group is in part the result of extinction of fossil plants with intermediate morphologies, and report evidence of a pattern of episodic sharp increases of morphological diversity throughout the evolutionary history of plants.[191]
A study on the evolution of the complexity of vascular plant reproductive structures, indicating that major reproductive innovations were associated with increased integration through greater interactions among component parts, is published by Leslie & Mander (2023).[192]
Evidence from mercury concentration and isotopic signatures of marine sedimentary rock samples spanning from the Cambrian to Permian, interpreted as indicating that vascular plants were already widely distributed on land during the Ordovician-Silurian transition, is presented by Yuan et al. (2023).[193]
Evidence indicating that the knowledge of the early plant diversity from the latest Silurian–Early Devonian fossil record is at least partly affected by the variation of the rock record is presented by Capel et al. (2023).[194]
A study on early land plant diversity patterns across known paleogeographical units (Laurussia, Siberia, Kazakhstania, Gondwana) throughout the Silurian and Devonian periods is published by Capel et al. (2023)[195]
A study on the survivorship and migration dynamics of plants from the paleocontinent Angarida during the Frasnian-Tournaisian internal, as indicated by fossil record from the Siberian platform (Russia), is published by Dowding, Akulov & Mashchuk (2023).[196]
Barrón et al. (2023) study the floral assemblages from the Cretaceous Maestrazgo Basin (Spain), providing evidence of the existence of conifer woodlands and fern/angiosperm communities thriving in the mid-Cretaceous Iberian Desert System, and report that the studied assemblages can generally be related to others from Europe and North America, but also included plants that were typical for northern Gondwana.[197]
A study on the fossil material of plants from the Cenomanian deposits of the Western Desert (Egypt) is published by El Atfy et al. (2023), who report the presence of five main vegetation types, and interpret the studied fossils as indicative of an overall warm and humid climate, punctuated by repeated phases of drier conditions.[198]
Moreau & Néraudeau (2023) describe an assemblage of Cenomanian plants from a new paleontological site La Gripperie-Saint-Symphorien (Charente-Maritime, France), which (unlike most of Albian-Cenomanian coastal floras from the Aquitaine Basin) is dominated by angiosperms.[199]
A study on the mid-Eocene vegetation in the southern Central Andes, based on spore-pollen record from the Casa Grande Formation (Jujuy, Argentina), is published by Tapia et al. (2023), who interpret their findings as indicative of a plant community with no close analogue in the modern South American vegetation, as well as indicative of subtropical or tropical conditions and frost-free winters.[200]
Description of fossil wood from the Brown Sands and Flat Sands localities in the Pliocene Usno Formation (Lower Omo valley, Ethiopia) is published by Jolly-Saad & Bonnefille (2023), who report that the studied assemblages strongly differ from other Miocene and Pliocene wood assemblages from Ethiopia, and interpret them as indicative of a seasonal climate and more humid climatic conditions compared to the present, but also as indicative of instability of climatic and environmental conditions, with significant changes in the composition of the tree cover during the time of existence of Australopithecus afarensis.[201]
A study on changes in functional diversity of plants from southeast Australia during the last 12,000 years, inferred from long-term pollen records, is published by Adeleye et al. (2023).[202]
The oldest flower and seed fossils of the wind-pollinated besom heaths, Erica sect. Chlorocodon, were found in Madeira Island within a 1.3 million-year-old fossil deposit.[203]
References
^ abcKhosla, A.; Verma, O.; Kania, S.; Lucas, S. (2023). "Indian Late Cretaceous-Early Palaeocene Deccan Microbiota from the Intertrappean Beds of the Chhindwara District, Madhya Pradesh and Their Systematic Palaeontology". In A. Khosla; O. Verma; S. Kania; S. Lucas (eds.). Microbiota from the Late Cretaceous-Early Palaeocene Boundary Transition in the Deccan Intertrappean Beds of Central India. Topics in Geobiology. Vol. 54. Springer. pp. 77–205. doi:10.1007/978-3-031-28855-5_4. ISBN978-3-031-28854-8.
^Xing, Y.; Li, S.; Song, B.; Jiang, G.; Wei, Y.; Han, F.; Zhang, K. (2023). "Middle to late Eocene charophytes from the Gaize Basin in central Tibet". Review of Palaeobotany and Palynology. 321. 105024. doi:10.1016/j.revpalbo.2023.105024.
^ abcPerez Loinaze, V. S.; Vera, E. I.; Moyano-Paz, D.; Coronel, M. D.; Manabe, M.; Tsuihiji, T.; Novas, F. E. (2023). "Maastrichtian palynological assemblages from the Chorrillo Formation, Patagonia, Argentina". Review of Palaeobotany and Palynology. 314. 104893. Bibcode:2023RPaPa.31404893P. doi:10.1016/j.revpalbo.2023.104893. S2CID258043990.
^LoDuca, S. T. (2024). "Reinterpretation of Voronocladus from the Silurian of Ukraine as a bryopsidalean alga (Chlorophyta): The outlines of a major early Paleozoic macroalgal radiation begin to come into focus". Review of Palaeobotany and Palynology. 322. 105064. doi:10.1016/j.revpalbo.2024.105064.
^Xiang, K.; Yin, Z.; Liu, W.; Zhao, F.; Zhu, M. (2023). "Early Cambrian Cambroclavus is a scleritomous eumetazoan unrelated to bryozoan or dasyclad algae". Geology. 52 (2): 130–134. doi:10.1130/G51663.1.
^Spiekermann, R.; Jasper, A.; Pozzebon-Silva, Â.; Carniere, J. S.; Benício, J. R. W.; Guerra-Sommer, M.; Uhl, D. (2023). "Small but not trivial: Nothostigma sepeensis sp. nov., a lycopsid from the Cisuralian (early Permian) of the Paraná Basin, Brazil". Journal of South American Earth Sciences. 122: 104188. Bibcode:2023JSAES.12204188S. doi:10.1016/j.jsames.2022.104188. S2CID255249522.
^ abBek, J.; Pšenička, J.; Drábková, J.; Zhou, W.-M.; Wang, J. (2023). "Thomasites gen. nov. a new herbaceous lycophyte and its spores from late Duckmantian of the Radnice Basin, Czech Republic and palynological grouping of Palaeozoic herbaceous lycophytes". Review of Palaeobotany and Palynology. 310. 104842. Bibcode:2023RPaPa.31004842B. doi:10.1016/j.revpalbo.2023.104842. S2CID255799382.
^Cichan, M. A. (1985). "Vascular cambium and wood development in Carboniferous plants. I. Lepidodendrales". American Journal of Botany. 72 (8): 1163–1176. doi:10.2307/2443396. JSTOR2443396.
^D'Antonio, M. P. (2023). "Atypical tracheid organization in proximal wood of late Palaeozoic Sigillaria approximata Fontaine et White (Lycopsida)". Botanical Journal of the Linnean Society. 203 (3): 303–314. doi:10.1093/botlinnean/boad028.
^Zhou, W.; Pšenička, J.; Bek, J.; Libertín, M.; Wang, S.; Wang, J. (2023). "A new species of Botryopteridium Doweld from the early Permian Wuda Tuff Flora and its evolutionary significance". Review of Palaeobotany and Palynology. 311. 104849. Bibcode:2023RPaPa.31104849Z. doi:10.1016/j.revpalbo.2023.104849. S2CID256151569.
^Fernández, J. A.; Césari, S. N. (2023). "Equisetaleans from the Bajo de Veliz Formation (Gzhelian-Asselian): a new key in the evolution of Gondwanan reproductive structures". Historical Biology. 36 (9): 1712–1726. doi:10.1080/08912963.2023.2228331.
^Pšenička, J.; Votočková Frojdová, J.; Bek, J.; Zodrow, E. L.; Zhou, W.-M.; Wang, J.; Li, D.-D.; Feng, Z.; Guo, Y.; Zhou, Y. (2023). "A new marattialean fern Diplazites campbellii sp. nov. and its in situ spores from the Pennsylvanian of the Sydney Coalfield, Nova Scotia, Canada". Review of Palaeobotany and Palynology. 312. 104850. Bibcode:2023RPaPa.31204850P. doi:10.1016/j.revpalbo.2023.104850. S2CID256125643.
^ abKerp, H.; Krause, K. K.; Abu Hamad, A.; Bomfleur, B. (2023). "Early Marattiaceae from the late Permian Umm Irna Formation, Jordan". Review of Palaeobotany and Palynology. 322. 105015. doi:10.1016/j.revpalbo.2023.105015.
^Ren, W. X.; Wu, G. T.; Han, L.; Hua, Y. F.; Sun, B. N. (2023). "New species of fossil Dryopterites from the Lower Cretaceous in the Zhongkouzi Basin, Beishan area, Northwest China, and its geological significance". Historical Biology. 35 (1): 84–91. Bibcode:2023HBio...35...84R. doi:10.1080/08912963.2021.2022135. S2CID245694205.
^ abCao, Z.-D.; Zhang, P.; Zhang, S.-H.; Yang, Y.-H.; Chen, J.-Y.; Liu, L.-M.; Li, X.-C.; Xie, S.-P. (2023). "Miocene Equisetum tubers from the Wulan Basin, Northeast Qinghai-Tibetan Plateau and their paleoecological significance". Palaeoworld. 33: 216–228. doi:10.1016/j.palwor.2022.12.012. S2CID255658320.
^Long, X.; Peng, Y.; Zhang, H.; Fan, Y.; Shi, C.; Wang, S. (2023). "Microlepia burmasia sp. nov., a new fern species from mid-Cretaceous Kachin amber of northern Myanmar (Dennstaedtiaceae, Polypodiales)". Cretaceous Research. 143. 105417. Bibcode:2023CrRes.14305417L. doi:10.1016/j.cretres.2022.105417. S2CID253494172.
^Zhang, W. (2024). "Comment on «Microlepia burmasia sp. nov., a new fern species from mid-Cretaceous Kachin amber of norther Myanmar (Dennstaedtiaceae, Polypodiales) » [Cretaceous Research 143 (2023) 105417]". Cretaceous Research. 166. 106010. doi:10.1016/j.cretres.2024.106010.
^Kundu, S.; Hazra, T.; Chakraborty, T.; Bera, S.; Taral, S.; Khan, M. A. (2023). "First Cenozoic macrofossil record of Polypodiaceae from India, and its biogeographic implications". International Journal of Plant Sciences. 185 (1): 71–88. doi:10.1086/727457.
^Long, X.; Peng, Y.; Feng, Q.; Engel, M. S.; Shi, C.; Wang, S. (2023). "A new fossil fern of the Dryopteridaceae (Polypodiales) from the mid-Cretaceous Kachin amber". Palaeobiodiversity and Palaeoenvironments. 103 (3): 489–494. doi:10.1007/s12549-023-00572-4. S2CID257253460.
^Guo, Y.; Zhou, Y.; Pšenička, J.; Bek, J.; Votočková Frojdová, J.; Feng, Z. (2023). "Szea yunnanensis sp. nov., a new leptosporangiate fern from the Lopingian of Southwest China". Review of Palaeobotany and Palynology. 320. 105022. doi:10.1016/j.revpalbo.2023.105022.
^Walker, Z.; Rothwell, G. W.; Stockey, R. A. (2023). "Fossil evidence for sporeling development of a Mesozoic osmundaceous fern". American Journal of Botany. 110 (8). e16210. doi:10.1002/ajb2.16210. PMID37534408.
^Blanco-Moreno, C.; Buscalioni, Á. D. (2023). "Revision of the Barremian fern Coniopteris laciniata from Las Hoyas and El Montsec (Spain): Highlighting its importance in the evolution of vegetation during the Early Cretaceous". Taxon. 72 (3): 625–637. doi:10.1002/tax.12888. hdl:10486/707335. S2CID258044454.
^ abcMartínez, L. C. A.; Leppe, M.; Manríquez, L. M. E.; Pino, J. P.; Trevisan, C.; Manfroi, J.; Mansilla, H. (2023). "A unique Late Cretaceous fossil wood assemblage from Chilean Patagonia provides clues to a high-latitude continental environment". Papers in Palaeontology. 9 (6). e1536. doi:10.1002/spp2.1536.
^Li, Q.; Niu, B.; Liu, Y. C.; Jia, H.; Li, Y.; Xu, L.; Quan, C. (2023). "Analysis of leaf economics sheds light on the heterophylly and ecological strategies of Paleocene Ginkgo leaves from Henan Province, China". Palaeogeography, Palaeoclimatology, Palaeoecology. 630. 111816. doi:10.1016/j.palaeo.2023.111816.
^ abNosova, N.; Kostina, E.; Afonin, M. (2023). "Ovule-bearing structures of Karkenia Archangelsky and associated leaves of Sphenobaiera Florin from the Lower Cretaceous of Mongolia". Review of Palaeobotany and Palynology. 315. 104907. Bibcode:2023RPaPa.31504907N. doi:10.1016/j.revpalbo.2023.104907. S2CID258682134.
^Kvaček, J.; Mendes, M. M.; Tekleva, M. (2023). "A new cheirolepidiaceous pollen cone Classostrobus archangelskyi with in situ pollen from the Lower Cretaceous of Figueira da Foz Formation, central-western mainland Portugal". Review of Palaeobotany and Palynology. 104951. doi:10.1016/j.revpalbo.2023.104951.
^Jin, P.; Zhang, M.; Du, B.; Li, A.; Sun, B. (2023). "A new species of Pararaucaria from the Lower Cretaceous of Shandong province (Eastern China): Insights into the Evolution of the Cheirolepidiaceae cone". Cretaceous Research. 146. 105475. Bibcode:2023CrRes.14605475J. doi:10.1016/j.cretres.2023.105475. S2CID256537440.
^Mendes, M. M.; Kvaček, J.; Doyle, J. A. (2023). "Pseudofrenelopsis dinisii, a new species of the extinct conifer family Cheirolepidiaceae from the probable lower Hauterivian (Cretaceous) of western Portugal". Review of Palaeobotany and Palynology. 315. 104905. Bibcode:2023RPaPa.31504905M. doi:10.1016/j.revpalbo.2023.104905. S2CID258536399.
^Kvaček, J.; Mendes, M.M. (2023). "A new species of the cheirolepidiaceous conifer Pseudofrenelopsis from the Lower Cretaceous of Figueira da Foz Formation, Portugal". Review of Palaeobotany and Palynology. 309 (104821): 104821. doi:10.1016/j.revpalbo.2022.104821. hdl:10316/104361.
^Correia, P.; Pereira, S.; Šimůnek, Z.; Cleal, C. J. (2023). "Florinanthus bussacensis sp. nov., a new cordaitalean cone from the Upper Pennsylvanian of Portugal". Review of Palaeobotany and Palynology. 316. 104942. doi:10.1016/j.revpalbo.2023.104942.
^Sokolova, A. B.; Zavialova, N. E.; Moiseeva, M. G.; Kodrul, T. M. (2024). "The New Genus Amurodendron (Cupressaceae s.l.) from the Paleocene Boguchan Flora of the Amur Region (Russian Far East)". Paleontological Journal. 57 (10): 1188–1211. doi:10.1134/S0031030123100052.
^Guo, L.-Y.; Xiao, L.; Ji, D.-S.; Li, X.-C.; Luo, F.; Guo, J.-F.; Sun, N.; Wang, M.-T.; Ren, W.-X. (2023). "Juniperus L. (Cupressaceae) from the Miocene of Chifeng, Inner Mongolia: the earliest macrofossil of sect. Sabina in East Asia". Historical Biology. 36 (10): 2196–2208. doi:10.1080/08912963.2023.2248162.
^Rothwell, G. W.; Stockey, R. A.; Smith, S. (2023). "Evolutionary diversification of taiwanioid conifers illuminated by a new species from the Upper Cretaceous of Alaska". International Journal of Plant Sciences. 184 (8): 628–639. doi:10.1086/726082.
^Zhu, Y.; Li, Y.; Tian, N.; Wang, Y.; Xie, A.; Zhang, L.; An, P.; Wu, Z. (2023). "A new species of Keteleeria (Pinaceae) from the Lower Cretaceous of Inner Mongolia, Northeast China, and its palaeogeographic and palaeoclimatic implications". Cretaceous Research. 156. 105805. doi:10.1016/j.cretres.2023.105805.
^ abAndruchow-Colombo, A.; Rossetto-Harris, G.; Brodribb, T. J.; Gandolfo, M. A.; Wilf, P. (2023). "A new fossil Acmopyle with accessory transfusion tissue and potential reproductive buds: Direct evidence for ever-wet rainforests in Eocene Patagonia". American Journal of Botany. 110 (8). e16221. doi:10.1002/ajb2.16221. PMID37598386.
^ abcdefPujana, R. R.; Bostelmann, J. E.; Ugalde, R. A.; Riquelme, M. P.; Torres, T. (2022). "Fossil woods from the Pato Raro Heights, Patagonia National Park, Aysén, Chile: A new paleobotanical assemblage at the Oligocene climate transition". Review of Palaeobotany and Palynology. 309. 104814. doi:10.1016/j.revpalbo.2022.104814. S2CID254332837.
^Xie, A.; Wang, Y.; Tian, N.; Uhl, D. (2023). "A new extinct conifer Brachyoxylon from the Middle Jurassic in southern China: Wood anatomy, leaf phenology, and paleoclimate". Review of Palaeobotany and Palynology. 317. 104945. doi:10.1016/j.revpalbo.2023.104945.
^ abMorales-Toledo, J.; Cevallos-Ferriz, S. R. S. (2023). "Is biodiversity promoted in rift-associated basins? Evidence from Middle Jurassic conifers from the Otlaltepec Formation in Puebla, Mexico". Review of Palaeobotany and Palynology. 318. 104952. doi:10.1016/j.revpalbo.2023.104952.
^Nosova, N.; Lyubarova, A. (2023). "First data on coniferous leaves from the Middle Jurassic of the Belgorod Region, Russia". Review of Palaeobotany and Palynology. 317. 104949. doi:10.1016/j.revpalbo.2023.104949.
^Wang, K.; Huang, X.; Yang, W.; Wang, J.; Wan, M. (2023). "A new gymnospermous stem from the Moscovian (Carboniferous) of North China, and its palaeoecological significance for the Cathaysian Flora at the early evolutionary stage". Review of Palaeobotany and Palynology. 311. 104858. Bibcode:2023RPaPa.31104858W. doi:10.1016/j.revpalbo.2023.104858. S2CID256596362.
^Cai, Y.-F.; Zhang, H.; Feng, Z.; Zhang, Y.-C.; Yuan, D.-X.; Xu, H.-P.; Byambajav, U.; Yarinpuil, A.; Shen, S.-Z. (2023). "Secrospiroxylon tolgoyensis gen. nov. et sp. nov., a unique coniferous stem from the uppermost Permian of the South Gobi Basin, Mongolia, and its palaeoclimatic, palaeoecophysiological, and palaeoecological implications". Palaeontographica Abteilung B. 305 (1–4): 93–119. doi:10.1127/palb/2023/0080.
^Trümper, S.; Rößler, R.; Morelli, C.; Krainer, K.; Karbacher, S.; Vogel, B.; Antonelli, M.; Sacco, E.; Kustatscher, E. (2023). "A fossil forest from Italy reveals that wetland conifers thrived in Early Permian Peri-Tethyan Pangea". PALAIOS. 38 (10): 407–435. doi:10.2110/palo.2023.015.
^Slodownik, M. A.; Escapa, I.; Mays, C.; Jordan, G. J.; Carpenter, R. J.; Hill, R. S. (2023). "Araucarioides: A Polar Lineage of Araucariaceae with New Paleogene Fossils from Tasmania, Australia". International Journal of Plant Sciences. 184 (8): 640–658. doi:10.1086/726183.
^Andruchow-Colombo, A.; Escapa, I. H.; Aagesen, L.; Matsunaga, K. K. S. (2023). "In search of lost time: tracing the fossil diversity of Podocarpaceae through the ages". Botanical Journal of the Linnean Society. 203 (4): 315–336. doi:10.1093/botlinnean/boad027. hdl:11336/227952.
^Stockey, R. A.; Rothwell, G. W.; Beard, G.; Gemmell, J. (2023). "Refining Our Understanding of Late Cretaceous-Paleogene Evolution within the Monocot Family Araceae: Appianospadix bogneri gen. et sp. nov". International Journal of Plant Sciences. 184 (6): 470–484. doi:10.1086/725163. S2CID257860852.
^Kumar, S.; Khan, M. A. (2023). "First megafossil occurrence of Cryosophileae (Arecaceae) in Asia: anatomy, systematics, and biogeography". Botany Letters. 171 (2): 181–193. doi:10.1080/23818107.2023.2293111.
^Hamersma, A.; Herrera, F.; Matsunaga, K.; Manchester, S. R. (2023). "Palm fruits from the Oligocene of west coastal Peru". Review of Palaeobotany and Palynology. 320. 105018. doi:10.1016/j.revpalbo.2023.105018.
^Mahato, S.; Khan, M. A. (2024). "The First Fossil Record of Coryphoid Palm from Siwalik Strata (Middle Miocene) of Darjeeling Foothills of Eastern Himalaya". Paleontological Journal. 57 (3 supplement): S268 –S284. doi:10.1134/S003103012360004X.
^ abcHuegele, I. B.; Correa Narvaez, J. E. (2023). "Revisiting the iconic Macginitiea plant and its implications for biogeography, basilaminar lobe development, and evolution in Platanaceae". International Journal of Plant Sciences. 185 (2): 138–158. doi:10.1086/728411.
^Kara, E.; Bardin, J.; De Franceschi, D.; Del Rio, C. (2023). "Fossil endocarps of Menispermaceae from the late Paleocene of Paris Basin, France". Journal of Systematics and Evolution. 62 (4): 809–828. doi:10.1111/jse.13033.
^Bhatia, H.; Srivastava, G.; Mehrotra, R. C. (2023). "Cordiaceae wood from the Miocene sediments of northeast India and its phytogeographical significance". IAWA Journal. 45 (2): 154–166. doi:10.1163/22941932-bja10139.
^Poore, C.; Jud, N. A.; Gandolfo, M. A. (2023). "Fossil fruits from the early Paleocene of Patagonia, Argentina reveal west Gondwanan history of Icacinaceae". Review of Palaeobotany and Palynology. 317. 104940. doi:10.1016/j.revpalbo.2023.104940.
^ abAkkemik, Ü.; Toprak, Ö.; Mantzouka, D.; Çelik, H. (2023). "A Mediterranean woody species composition from Late Miocene-Early Pliocene deposits of northeastern Turkey with newly described fossil-taxa palaeoclimatically evaluated". Review of Palaeobotany and Palynology. 316. 104916. doi:10.1016/j.revpalbo.2023.104916.
^ abDeanna, R.; Martínez, C.; Manchester, S.; Wilf, P.; Campos, A.; Knapp, S.; Chiarini, F. E.; Barboza, G. E.; Bernardello, G.; Sauquet, H.; Dean, E.; Orejuela, A.; Smith, S. D. (2023). "Fossil berries reveal global radiation of the nightshade family by the early Cenozoic". New Phytologist. 238 (6): 2685–2697. doi:10.1111/nph.18904. PMID36960534. S2CID257715632.
^ abCorrea Narvaez, J. E.; Allen, S. E.; Huegele, I. B.; Manchester, S. R. (2023). "Fossil leaves and fruits of Tetramelaceae (Curcurbitales) from the Eocene of the Rocky Mountain region, USA, and their biogeographic significance". International Journal of Plant Sciences. 184 (3): 177–200. doi:10.1086/724018. S2CID256185427.
^Cockerell, T.D.A. (1925). "Plant and insect fossils from the Green River Eocene of Colorado". Proceedings of the U.S. National Museum. 66 (19): 1–13. doi:10.5479/si.00963801.66-2556.1.
^Wang, Z.X.; Sun, B.N.; Wu, X.T.; Yin, S.X. (2023). "A new pod record of Acacia (Leguminosae) from the Fotan Group, middle Miocene, Southeast China". Review of Palaeobotany and Palynology. 317. 104966. doi:10.1016/j.revpalbo.2023.104966.
^Pan, A. D.; Jacobs, B. F.; Currano, E. D.; de la Estrella, M.; Herendeen, P. S.; van der Burgt, X. M. (2023). "A fossil Anthonotha (Leguminosae: Detarioideae: Amherstieae) species from the Early Miocene (21.73 Ma) of Ethiopia". International Journal of Plant Sciences. 184 (7): 541–548. doi:10.1086/725429. hdl:2346/96779.
^Gao, Y.; Song, A.; Deng, W.-Y.-D.; Chen, L.-L.; Liu, J.; Li, W.-C.; Srivastava, G.; Spicer, R. A.; Zhou, Z.-K.; Su, T. (2023). "The oldest fossil record of Bauhinia s.s. (Fabaceae) from the Tibetan Plateau sheds light on its evolutionary and biogeographic implications". Journal of Systematic Palaeontology. 21 (1). 2244495. doi:10.1080/14772019.2023.2244495.
^Estrada-Ruiz, E.; Gómez-Acevedo, G.-A. (2023). "New species fossil of Entada genus (Fabaceae, Caesalpinioideae, mimosoid clade) from the Miocene amber of Chiapas, Mexico". Journal of South American Earth Sciences. 104499. doi:10.1016/j.jsames.2023.104499.
^Dutra, T. L.; Martínez, L. C. A.; Wilberger, T. (2023). "A new fossil wood of Detarioideae from the Boa Vista Basin, Upper Oligocene (Northeast Brazil): Comparisons with living and fossil Leguminosae Subfamilies. Paleoclimate and biogeography inferences for the Leguminosae story". Review of Palaeobotany and Palynology. 317. 104968. doi:10.1016/j.revpalbo.2023.104968.
^Hazra, T.; Bera, S.; Khan, M. A. (2023). "First Fossil Mallow Flower from Asia". International Journal of Plant Sciences. 184 (2): 106–121. doi:10.1086/723603. S2CID256356226.
^Zhao, Y.; Song, A.; Deng, W.; Huang, J.; Su, T. (2023). "Fossil leaves of Pterospermum (Malvaceae) from the Early Miocene of Jinggu, Yunnan Province with its paleoecological and phytogeographical implications". Quaternary Sciences. 43 (3): 884–898. doi:10.11928/j.issn.1001-7410.2023.03.16.
^ abcRamos, R. S.; Brea, M.; Kröhling, D. M.; Patterer, N. I. (2023). "Pleistocene subtribe Terminaliinae (Combretaceae) fossils in the middle-lower Uruguay river basin, South America". Review of Palaeobotany and Palynology. 311. 104857. Bibcode:2023RPaPa.31104857R. doi:10.1016/j.revpalbo.2023.104857. S2CID256492732.
^Bhatia, H.; Srivastava, G.; Mehrotra, R. C. (2023). "Duabanga (Lythraceae) from the Oligocene of India and its climatic and phytogeographic significance". Geobios. 78: 1–13. doi:10.1016/j.geobios.2023.05.003. S2CID258875041.
^Martínez, C.; Pérez-Lara, D. K.; Avellaneda-Jiménez, D. S.; Caballero-Rodríguez, D.; Rodríguez-Reyes, O.; Crowley, J. L.; Jaramillo, C. (2023). "An early Miocene (Aquitanian) mangrove fossil forest buried by a volcanic lahar at Barro Colorado Island, Panama". Palaeogeography, Palaeoclimatology, Palaeoecology. 637. 112006. doi:10.1016/j.palaeo.2023.112006.
^Wu, X.-T.; Wang, Z.-X.; Shu, J.-W.; Yin, S.-X.; Mao, L.-M.; Shi, G.-L. (2023). "A new Trapa from the middle Miocene of Zhangpu, Fujian, southeastern China". Palaeoworld. 32 (4): 618–625. doi:10.1016/j.palwor.2023.02.008. S2CID257370975.
^Patel, R.; Rana, R. S.; Ali, A.; Hazra, T.; Khan, M. A. (2023). "First buckthorn (Rhamnaceae) fossil flowers from India". Journal of Systematics and Evolution. 62 (4): 829–841. doi:10.1111/jse.13024.
^Lu, P.; Zhang, J.-W.; Liang, X.-Q.; Li, H.-M.; Li, D.-L. (2023). "Ancestors of Ulmus parvifolia from late Miocene sediments in Yunnan, Southwest China and its future distribution". Review of Palaeobotany and Palynology. 313. 104879. Bibcode:2023RPaPa.31304879L. doi:10.1016/j.revpalbo.2023.104879. S2CID257650454.
^ abKumar, S.; Manchester, S.; Judd, W.; Khan, M. (2023). "Earliest fossil record of Burseraceae from the Deccan Intertrappean Beds of Central India and its biogeographic implications". International Journal of Plant Sciences. 184 (9): 696–714. doi:10.1086/726627.
^ abRombola, C. F.; Pujana, R. R.; Ruiz, D. P.; Bellosi, E. S. (2023). "Angiosperm fossil woods from the Upper Cretaceous (Cardiel Formation) of Argentinean Patagonia". Botanical Journal of the Linnean Society. 205 (2): 132–149. doi:10.1093/botlinnean/boad072.
^ abBeurel, S.; Bachelier, J. B.; Hammel, J. U.; Shi, G.-L.; Wu, X.-T.; Rühr, P. T.; Sadowski, E.-M. (2023). "Flower inclusions of Canarium (Burseraceae) from Miocene Zhangpu amber (China)". Palaeoworld. 32 (4): 592–606. doi:10.1016/j.palwor.2023.02.006. S2CID257274673.
^Manchester, S. R.; Kapgate, D. K.; Judd, W. S. (2023). "Burseraceae in the latest Cretaceous of India: Sahniocarpon Chitaley & Patil". International Journal of Plant Sciences. 185 (3): 291–300. doi:10.1086/729091.
^Chandra, K.; Shukla, A.; Mehrotra, R. C.; Bansal, M.; Prasad, V. (2023). "Fossil Mahogany from the Early Paleogene of India". Journal of the Geological Society of India. 99 (1): 65–72. doi:10.1007/s12594-023-2268-2. S2CID256146833.
^ abMaslova, N. P.; Kodrul, T. M.; Kachkina, V. V.; Hofmann, C.-C.; Xu, S.-L.; Liu, X.-Y.; Jin, J.-H. (2023). "Evidence for the evolutionary history and diversity of fossil sweetgums: leaves and associated capitate reproductive structures of Liquidambar from the Eocene of Hainan Island, South China". Papers in Palaeontology. 9 (6). e1540. doi:10.1002/spp2.1540.
^Wu, X.-T.; Shu, J.-W.; Yin, S.-X.; Sadowski, E.-M.; Shi, G.-L. (2023). "Parrotia flower blooming in Miocene rainforest". Journal of Systematics and Evolution. 62 (3): 449–456. doi:10.1111/jse.13001.
^Tang, K. K.; Smith, S. Y.; Atkinson, B. A. (2023). "Winged Fruits of Friisifructus aligeri gen. et sp. nov. from the Late Cretaceous of Western North America". International Journal of Plant Sciences. 184 (4): 271–281. doi:10.1086/724745. S2CID257989759.
^ abČepičková, J.; Kvaček, J. (2022). "Fossil leaves of Cenomanian basal angiosperms from the Peruc-Korycany Formation, Czechia, central Europe". Review of Palaeobotany and Palynology. 309. 104802. doi:10.1016/j.revpalbo.2022.104802. S2CID253504307.
^Mahato, S.; Hazra, T.; More, S.; Khan, M. A. (2023). "Triplinerved cinnamon from the Siwalik (middle Miocene) of eastern Himalaya: Systematics, epifoliar fossil fungi, palaeoecology and biogeography". Geobios. 82: 53–67. doi:10.1016/j.geobios.2023.10.003.
^Čepičková, J.; Kvaček, J. (2023). "Papillaephyllum, a new genus of angiosperm foliage from the Cenomanian of the Czech Republic". Review of Palaeobotany and Palynology. 319. 104990. doi:10.1016/j.revpalbo.2023.104990.
^Friis, E. M.; Crane, P. R.; Pedersen, K. R. (2023). "Multipartite Flowers with a Distinct Floral Cup and Multiovulate Carpels: An Early Cretaceous Angiosperm of Probable Lauralean Relationship". International Journal of Plant Sciences. 184 (2): 87–105. doi:10.1086/723682. S2CID255675031.
^Pessoa, E. M.; Ribeiro, A. C.; Christenhuz, M. J. M.; Coan, A. I.; Jud, N. A. (2023). "Is Santaniella a ranuculid? Re-assessment of this enigmatic fossil angiosperm from the Lower Cretaceous (Aptian, Crato Konservat-Lagerstätte, Brazil) provides a new interpretation". American Journal of Botany. 110 (5). e16163. doi:10.1002/ajb2.16163. PMID37014186. S2CID257922833.
^Pessoa, E. M.; Ribeiro, A. C.; Christenhusz, M. J. M. (2023). "New evidence on the previously unknown gynoecium of Araripia florifera (Araripiaceae, fam. nov.), a magnoliid angiosperm from the Lower Cretaceous (Aptian) of the Crato Konservat-Lagerstätte (Araripe Basin), northeastern Brazil". Cretaceous Research. 153. 105715. doi:10.1016/j.cretres.2023.105715.
^López-Martínez, A. M.; Schönenberger, J.; von Balthazar, M.; González-Martínez, C. A.; Ramírez-Barahona, S.; Sauquet, H.; Magallón, S. (2023). "Integrating Fossil Flowers into the Angiosperm Phylogeny Using Molecular and Morphological Evidence". Systematic Biology. 72 (4): 837–855. doi:10.1093/sysbio/syad017. PMID36995161.
^Doyle, J.; Endress, P. K. (2023). "Integrating Cretaceous fossils into the phylogeny of living angiosperms: fossil Magnoliales and their evolutionary implications". International Journal of Plant Sciences. 185 (1): 42–70. doi:10.1086/727523.
^Lamont, B. B.; Ladd, P. G. (2024). "Endobeuthos paleosum in 99-million-year-old amber does not belong to the Proteaceae". Journal of the Botanical Research Institute of Texas. 18 (1): 143–147. doi:10.17348/jbrit.v18.i1.1343.
^Liu, B.-C.; Zong, R.-W.; Wang, K.; Bai, J.; Wang, Y.; Xu, H.-H. (2023). "Evolution of Silurian phytogeography, with the first report of Aberlemnia (Rhyniopsida) from the Pridoli of West Junggar, Xinjiang, China". Palaeogeography, Palaeoclimatology, Palaeoecology. 633. 111903. doi:10.1016/j.palaeo.2023.111903.
^Libertín, M.; Kvaček, J.; Bek, J. (2023). "The genus Aberlemnia and its Silurian–Devonian fossil record". Review of Palaeobotany and Palynology. 320. 105017. doi:10.1016/j.revpalbo.2023.105017.
^Brea, M.; Gnaedinger, S.; Martínez, L. C. A. (2023). "Archangelskyoxylon carlquistii gen. et sp. nov. Taxonomy and phylogeny of an unequivocal gnetoid Jurassic fossil wood". Review of Palaeobotany and Palynology. 105035. doi:10.1016/j.revpalbo.2023.105035.
^Uhlířová, M.; Pšenička, J.; Sakala, J. (2023). "New early land plant Capesporangites petrkraftii gen. et sp. nov. from the Silurian, Prague Basin, Czech Republic". Review of Palaeobotany and Palynology. 322. 105048. doi:10.1016/j.revpalbo.2023.105048.
^Luthardt, L.; Rößler, R.; Stevenson, D. W. (2023). "Cycadodendron galtieri gen. nov. et sp. nov. - A lower Permian gymnosperm stem with cycadalean affinity". International Journal of Plant Sciences. 184 (9): 715–732. doi:10.1086/727458.
^Barbacka, M.; Górecki, A.; Pott, C.; Ziaja, J.; Blodgett, R. B.; Metzler, C.; Caruthers, A. H.; Edirisooriya, G.; Pacyna, G. (2023). "Macroflora from Lower Jurassic (Pliensbachian) of Hicks Creek, southern Talkeetna Mountains, south-central Alaska". Papers in Palaeontology. 9 (6). e1541. doi:10.1002/spp2.1541.
^ abcdefghijkAnderson, J. M.; Anderson, H. M. (2023). "Molteno Kannaskoppia: Mid-Triassic gymnosperm case study for whole-plant taxonomy". Palaeontologia Africana. 57: 1–324. hdl:10539/37107.
^Lalica, M. A. K.; Tomescu, A. M. F. (2023). "Complex wound response mechanisms and phellogen evolution – insights from Early Devonian euphyllophytes". New Phytologist. 239 (1): 388–398. doi:10.1111/nph.18926. PMID37010090. S2CID257910880.
^Vallois, B.; Nel, A. (2023). "Possible earliest evidence of insect pollination based on a new species of the Carboniferous medullosalean 'seed' genus Pachytesta". Review of Palaeobotany and Palynology. 316. 104948. doi:10.1016/j.revpalbo.2023.104948.
^Trajano, A. D. E. S.; Marques-de-Souza, J.; Iannuzzi, R.; Holanda, E. C. (2023). "Ephedra-like Cones from Serra do Tucano formation (Lower Cretaceous), Takutu Basin, Roraima". Journal of South American Earth Sciences. 132: 104659. doi:10.1016/j.jsames.2023.104659.
^Pfeiler, K. C.; Tomescu, A. M. F. (2023). "Mosaic assembly of regulatory programs for vascular cambial growth: a view from the Early Devonian". New Phytologist. 240 (2): 529–541. doi:10.1111/nph.19146. PMID37491742.
^ abLi, A.; Du, B.; Peng, J.; Lin, S.; Zhang, J.; Ma, G.; Hui, J. (2023). "Leaves and megasporophylls of Cycadophytes from the Lower Cretaceous of Beishan area, Gansu Province, Northwest China, and its evolutionary significance". Cretaceous Research. 105636. doi:10.1016/j.cretres.2023.105636.
^Yang, X.-J. (2023). "First record of Rhaphidopteris (Gymnospermae) from the Lower Jurassic of the Junggar Basin, Xinjiang, NW China". In J. Sha; S. M. Slater; V. Vajda; P. E. Olsen; H. Zhang (eds.). The Triassic and Jurassic of the Junggar Basin, China: Advances in Palaeontology and Environments. Geological Society, London, Special Publications. Vol. 538. The Geological Society of London. pp. 169–177. doi:10.1144/SP538-2021-191. S2CID258339074.
^Elgorriaga, A.; Atkinson, B. A. (2023). "Cretaceous pollen cone with three-dimensional preservation sheds light on the morphological evolution of cycads in deep time". New Phytologist. 238 (4): 1695–1710. doi:10.1111/nph.18852. PMID36943236. S2CID257639494.
^Forte, G.; Kustatscher, E. I. (2023). "Cordaites and pteridosperm-like foliage from the Kungurian (early Permian) flora of Tregiovo (Trento, NE Italy)". Review of Palaeobotany and Palynology. 316. 104931. doi:10.1016/j.revpalbo.2023.104931.
^Blanco-Moreno, C.; Valois, M.; Stockey, R. A.; Rothwell, G. W.; Tomescu, A. M. F. (2023). "A Second Species of Tricosta Expands the Diversity of the Intriguing Mesozoic Tricostate Mosses". International Journal of Plant Sciences. 184 (7): 549–561. doi:10.1086/726016.
^Xie, A.; Teng, X.; Wang, Y.; Tian, N.; Jiang, Z.; Uhl, D. (2023). "A quantitative analysis of leaf life span reveals the Mesozoic boreal gymnosperm Xenoxylon as evergreen: First evidence from the Lower Cretaceous in Liaoning, northeastern China". Cretaceous Research. 105770. doi:10.1016/j.cretres.2023.105770.
^Xie, A.; Wang, Y.; Tian, N.; Xie, X.; Xi, S.; Uhl, D. (2023). "New occurrence of the Late Jurassic Xenoxylon wood in the Sichuan Basin, southern China: wood anatomy, and paleobiodiversity implications". PalZ. 98: 5–15. doi:10.1007/s12542-023-00671-9.
^Elgorriaga, A.; Atkinson, B. A. (2023). "Zirabia cylindrica comb. nov. provides evidence of Doyleales in the Jurassic". American Journal of Botany. 110 (7). e16182. doi:10.1002/ajb2.16182. PMID37272508.
^Flores, J. R.; Bippus, A. C.; Fernández de Ullivarri, C.; Suárez, G. M.; Hyvönen, J.; Tomescu, A. M. F. (2023). "Dating the evolution of the complex thalloid liverworts (Marchantiopsida): total-evidence dating analysis supports a Late Silurian-Early Devonian origin and post-Mesozoic morphological stasis". New Phytologist. 240 (5): 2137–2150. doi:10.1111/nph.19254. PMID37697646.
^Kipp, M. A.; Stüeken, E. E.; Strömberg, C. A. E.; Brightly, W. H.; Arbour, V. M.; Erdei, B.; Hill, R. S.; Johnson, K. R.; Kvaček, J.; McElwain, J. C.; Miller, I. M.; Slodownik, M.; Vajda, V.; Buick, R. (2023). "Nitrogen isotopes reveal independent origins of N2-fixing symbiosis in extant cycad lineages". Nature Ecology & Evolution. 8 (1): 57–69. doi:10.1038/s41559-023-02251-1. hdl:10023/28871. PMID37974002.
^ abcdParmar, S.; Morley, R. J.; Bansal, M.; Singh, B. P.; Morley, H.; Prasad, V. (2023). "Evolution of family Arecaceae on the Indian Plate modulated by the Early Palaeogene climate and tectonics". Review of Palaeobotany and Palynology. 313. 104890. Bibcode:2023RPaPa.31304890P. doi:10.1016/j.revpalbo.2023.104890. S2CID257872022.
^ abcdefghijklmnopqrstuvwxDe Benedetti, F.; Zamaloa, M. C.; Gandolfo, M. A.; Cúneo, N. R. (2023). "Pollen from the K–Pg boundary of the La Colonia Formation, Patagonia, Argentina". Review of Palaeobotany and Palynology. 316. 104933. doi:10.1016/j.revpalbo.2023.104933.
^Sui, Q.; Zhan, H.-X.; Zhou, D.-C.; Niu, Y.-N.; Chen, J.; McLoughlin, S.; Feng, Z. (2023). "Morphology and wall ultrastructure of a unique megaspore, Flabellisporites zhaotongensis Sui, McLoughlin et Feng sp. nov., from the upper Permian of Southwest China". Review of Palaeobotany and Palynology. 321. 105036. doi:10.1016/j.revpalbo.2023.105036.
^Quetglas, M. A.; Di Pasquo, M.; Macluf, C. C. (2023). "Taxonomy of Early Mississippian gulate megaspore assemblage from northern Bolivia". Review of Palaeobotany and Palynology. 318. 104971. doi:10.1016/j.revpalbo.2023.104971.
^Heřmanová, Z.; Kvaček, J.; Čepičková, J.; von Balthazar, M.; Luthardt, L.; Schönenberger, J. (2023). "Slavicekia gen. nov. - a new member of the Normapolles complex from Late Cretaceous sediments of the Czech Republic". International Journal of Plant Sciences. 184 (3): 201–213. doi:10.1086/724155. S2CID256048862.
^Zavialova, N. (2024). "Comment on "The 'seed-fern' Lepidopteris mass-produced the abnormal pollen Ricciisporites during the end-Triassic biotic crisis" by V. Vajda, S. McLoughlin, S. M. Slater, O. Gustafsson, and A. G. Rasmusson [Palaeogeography, Palaeoclimatology, Palaeoecology, 627 (2023), 111,723]". Review of Palaeobotany and Palynology. 322. 105065. doi:10.1016/j.revpalbo.2024.105065.
^Adeleye, M. A.; Haberle, S. G.; Gallagher, R.; Andrew, S. C.; Herbert, A. (2023). "Changing plant functional diversity over the last 12,000 years provides perspectives for tracking future changes in vegetation communities". Nature Ecology & Evolution. 7 (2): 224–235. doi:10.1038/s41559-022-01943-4. PMID36624175. S2CID255569024.
