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2025 in paleobotany

From Wikipedia, the free encyclopedia

List of years in paleobotany
In paleontology
2022
2023
2024
2025
2026
2027
2028
In arthropod paleontology
2022
2023
2024
2025
2026
2027
2028
In paleoentomology
2022
2023
2024
2025
2026
2027
2028
In paleomalacology
2022
2023
2024
2025
2026
2027
2028
In reptile paleontology
2022
2023
2024
2025
2026
2027
2028
In archosaur paleontology
2022
2023
2024
2025
2026
2027
2028
In mammal paleontology
2022
2023
2024
2025
2026
2027
2028
In paleoichthyology
2022
2023
2024
2025
2026
2027
2028

This paleobotany list records new fossil plant taxa that were to be described during the year 2025, as well as notes other significant paleobotany discoveries and events which occurred during 2025.

Algae

[edit]

Chlorophytes

[edit]
Name Novelty Status Authors Age Unit Location Synonymized taxa Notes Images

Morelletpora sinica[1]

Sp. nov

Valid

Schlagintweit, Xu & Zhang

Late Cretaceous (Campanian)

Yigeziya Formation

 China

A member of Dasycladales belonging to the family Triploporellaceae.

Phycological research

[edit]
  • A study on the reproduction of Eugonophyllum, based on fossils from the Carboniferous (Gzhelian) Maping Formation (Guizhou, China), is published by Wang et al. (2025).[2]

Non-vascular plants

[edit]

Marchantiophyta

[edit]
Name Novelty Status Authors Age Unit Location Synonymized taxa Notes Images

Frullania chiapasensis[3]

Sp. nov

Valid

Mamontov, Feldberg, Schäfer-Verwimp & Gradstein in Feldberg et al.

Miocene

Mexican amber

 Mexico

A liverwort, a species of Frullania.

Hyponychium[4]

Gen. et sp. nov

Paulsen et al.

Eocene

Anglesea amber

 Australia

A liverwort belonging to the group Jungermanniales. The type species is H. pentadactylum.

Radula panduriformis[4]

Sp. nov

Paulsen et al.

Eocene

Anglesea amber

 Australia

A liverwort, a species of Radula.

Thysananthus patrickmuelleri[3]

Sp. nov

Valid

Feldberg, Gradstein, Schäfer-Verwimp & Mamontov in Feldberg et al.

Miocene

Mexican amber

 Mexico

A liverwort belonging to the group Porellales and the family Lejeuneeae.

Lycophytes

[edit]
Name Novelty Status Authors Age Unit Location Synonymized taxa Notes Images

Selaginella jorelisiae[5]

Sp. nov

Valid

López-García, Schmidt & Regalado in López-García et al.

Miocene

Dominican amber

 Dominican Republic

A species of Selaginella.

Zosterophyllum baoyangense[6]

Sp. nov

Huang & Xue in Huang et al.

Devonian (Pragian)

Mangshan Group

 China

Ferns and fern allies

[edit]
Name Novelty Status Authors Age Unit Location Synonymized taxa Notes Images

Coniopteris haifanggouensis[7]

Sp. nov

Li & Tian in Li et al.

Middle Jurassic

Haifanggou Formation

 China

A member of the family Dicksoniaceae.

Krameropteris calophyllum[8]

Sp. nov

Li in Li & Meng

Late Cretaceous (Cenomanian)

Kachin amber

 Myanmar

A member of the family Dennstaedtiaceae.

Conifers

[edit]

Pinaceae

[edit]
Name Novelty Status Authors Age Unit Location Synonymized taxa Notes Images

Pinus longlingensis[9]

Sp. nov

Song & Wu in Song et al.

Pliocene

Mangbang Formation

 China

A pine.

Pinuxylon anatolica[10]

Sp. nov

Akkemik & Mantzouka

Miocene

Hançili Formation

 Turkey

A member of the family Pinaceae.

Podocarpaceae

[edit]
Name Novelty Status Authors Age Unit Location Synonymized taxa Notes Images

Metapodocarpoxylon brasiliense[11]

Sp. nov

Conceição et al.

Missão Velha Formation

 Brazil

Gnetophyta

[edit]
Name Novelty Status Authors Age Unit Location Synonymized taxa Notes Images

Ephedra transversa[12]

Sp. nov

Song & Wu in Li et al.

Early Cretaceous

Yixian Formation

 China

A species of Ephedra.

Flowering plants

[edit]

Monocots

[edit]

Monocot research

[edit]
  • Khan et al. (2025) describe fossil material of palms with one metaxylem vessel in each fibrovascular bundle from the Maastrichtian-Danian Deccan Intertrappean Beds (India), and interpret the studied fossils as Cocos-type palms belonging to the subfamily Arecoideae that likely grew in a tropical rainforest.[13]
  • Evidence from the study of phytoliths from the Giraffe locality (Northwest Territories, Canada), indicative of presence of palms close to the Arctic Circle over an extensive period of time during the Eocene (approximately 48 million years ago), is presented by Siver et al. (2025).[14]

Basal eudicots

[edit]
Name Novelty Status Authors Age Unit Location Synonymized taxa Notes Images

Palaeosinomenium indicum[15]

Sp. nov

Kumar, Manchester & Khan

Cretaceous-Paleocene (Maastrichtian-Danian)

Deccan Intertrappean Beds

 India

A member of the family Menispermaceae.
Announced in late 2024, published fully in 2025.

Proteaceaefolia[16]

Gen. et sp. nov

Carpenter & McLoughlin

Paleogene

 Chile

A member of the family Proteaceae. The type species is P. araucoensis.

Superasterids

[edit]

Apiales

[edit]
Name Novelty Status Authors Age Unit Location Synonymized taxa Notes Images

Astropanax eogetem[17]

Sp. nov

Pan et al.

Miocene

 Ethiopia

A species of Astropanax.

Icacinales

[edit]
Name Novelty Status Authors Age Unit Location Synonymized taxa Notes Images

Miquelia yenbaiensis[18]

Sp. nov

Hung, Huang & Li in Hung et al.

Miocene

Co Phuc Formation

 Vietnam

A species of Miquelia.

Superrosids

[edit]

Fabales

[edit]
Name Novelty Status Authors Age Unit Location Synonymized taxa Notes Images

Peltophorum xingjianii[19]

Sp. nov

Zhao, Wang & Huang in Zhao et al.

Miocene

Sanhaogou Formation

 China

A species of Peltophorum.

Pueraria qinghaiensis[20]

Sp. nov

Cao & Xie in Cao et al.

Miocene

Youshashan Formation

 China

A species of Pueraria.

Superrosid research

[edit]
  • Hazra & Khan (2025) report the discovery of a diverse assemblage of legume fruits and leaflet remains from the Rajdanda Formation (India), interpreted as evidence of the presence of a warm and humid tropical environment during the Pliocene.[21]
  • A study on the anatomy of wood of extant members of the genus Ficus and fossil wood with affinities to Ficus, and on its implications for determination of the organs preserved as fossil wood and their habits, is published by Monje Dussán, Pederneiras & Angyalossy (2025).[22]

Other angiosperms

[edit]
Name Novelty Status Authors Age Unit Location Synonymized taxa Notes Images

Menispermites temlyanensis[23]

Sp. nov

Zolina, Golovneva & Grabovskiy

Late Cretaceous–Paleocene (Maastrichtian–Danian)

Tanyurer Formation

 Russia
( Chukotka Autonomous Okrug)

A flowering plant with similarities to members of the genus Menispermum.

General angiosperm research

[edit]
  • A study on the timing of the evolution of the flowering plants is published by Ma et al. (2025), who recover the crown group of the flowering plants as likely originating in the Triassic.[24]
  • Doughty et al. (2025) use a mechanistic model to study the relationship between seed size of flowering plants, their light environment and the size of animals in their environment, and predict a rapid increase of seed size during the Paleocene that eventually plateaued or declined, likely as a result of the appearance of large herbivores that opened the understory, reducing the competitive advantage of plants with large seeds.[25]

Other plants

[edit]
Name Novelty Status Authors Age Unit Location Synonymized taxa Notes Images

Fengweioxylon[26]

Gen. et sp. nov

Valid

Jiang et al.

Jurassic

Tiaojishan Formation

 China

Fossil wood of a corystosperm. The type species is F. sinense.

Neuromariopteris[27]

Gen. et sp. nov

Šimůnek & Haldovský

Carboniferous (Bashkirian)

Kladno-Rakovník Basin

 Czech Republic

A member of Callistophytales. The type species is N. scandens.

Palaeopteridium andrenelii[28]

Sp. nov

Correia & Góis-Marques

Carboniferous (Moscovian)

 Portugal

A progymnosperm belonging to the group Noeggerathiales.

Shanxioxylon yangquanense[29]

Sp. nov

Wang & Wan in Wang et al.

Carboniferous (Kasimovian)

Benxi Formation

 China

A cordaitalean.

Yuzhoua[30]

Gen. et sp. nov

Wang, Lei & Fu

Permian (Asselian)

Lower Shihhotse Formation

 China

A plant of uncertain affinities, with similarities to the flowering plants. The type species is Y. juvenilis.

Other plant research

[edit]

Palynology

[edit]
Name Novelty Status Authors Age Unit Location Synonymized taxa Notes Images

Sparganiaceaepollenites intertrappeansis[32]

Nom. nov

DeBenedetti et al.

Late Cretaceous-Paleocene (Maastrichtian-Danian)

Mandla Formation

 India

Sparganiaceaepollenites annulatus Thakre et al. 2024 (junior homonym of S. annulatus De Benedetti, 2023).

Fossil pollen; a replacement name for Sparganiaceaepollenites reticulatus Samant et al. (2022).

Sparganiaceaepollenites oczkowicensis[32]

Nom. nov

DeBenedetti et al.

Miocene

 Poland

Fossil pollen; a replacement name for Sparganiaceaepollenites microreticulatus Grabowska & Ważyńska (2009).

Stigmatocystia[33]

Gen. et sp. nov

Strother et al.

Ordovician (Hirnantian)

Sarah Formation

 Saudi Arabia

Zygospores of a member of the family Zygnemataceae. The type species is S. divericata.

Zygnema paleopawneanum[33]

Sp. nov

Strother et al.

Ordovician (Hirnantian)

Sarah Formation

 Saudi Arabia

Zygospores of a member of the genus Zygnema.

Palynological research

[edit]
  • Nhamutole et al. (2025) study the composition of palynological assemblages from the Permian (Lopingian) strata of the Maniamba Basin (Mozambique), reporting evidence of the presence of plants indicative of lowland fluvial setting.[34]
  • Evidence from the study of palynofloral assemblages from the Germig Section (Qinghai-Tibetan Plateau; Tibet, China), interpreted as indicative of a shift from floras dominated by seed ferns and conifers to floras dominated by cheirolepids during the Triassic-Jurassic transition, is presented by Li et al. (2025).[35]
  • A study on palynofloral assemblages from the Las Loras UNESCO Global Geopark (Spain), providing evidence of gradual shift from conifer-dominated floras to ones with increased presence of flowering plants through the Albian–Cenomanian, is published by Rodríguez-Barreiro et al. (2025).[36]
  • Evidence from the study of palynomorph and palynofacies from the Bahariya Formation (Egypt), interpreted as indicative of warm and humid climate during the early-middle Cenomanian with a short episode of semi-arid to arid conditions during the late early Cenomanian, is presented by Abdelhalim et al. (2025).[37]
  • Rull (2025) revises purported fossil pollen records of Pelliciera found outside the Neotropics, and argues that only a subset of Cenozoic pollen records from tropical West Africa can be confirmed as likely fossils of members of Pelliciera.[38]
  • Evidence from the study of fossil pollen from the Dingqinghu Formation (China), indicative of presence of a mixed deciduous and coniferous forest in the central Qinghai-Tibet Plateau during the Oligocene-Miocene transition, is presented by Xie et al. (2025).[39]

General research

[edit]
  • Evidence from the study of fossil material from the South Taodonggou Section in the Turpan-Hami Basin (China), interpreted as indicative of presence of a refugium of land vegetation that preserved the stability of food chains during the Permian–Triassic extinction event and might have been one of the source regions for the diversification of terrestrial life in the aftermath of the extinction event, is presented by Peng et al. (2025).[40]
  • Evidence of a staggered recovery of plant communities from the Sydney Basin (Australia) in the aftermath of the Permian–Triassic extinction event, indicative of the presence of a succession gymnosperm-dominated and lycophyte-dominated plant communities lasting until the early Middle Triassic, is presented by Amores et al. (2025).[41]
  • Evidence of the presence of a plant community dominated by ferns belonging to the family Osmundaceae, similar to extant plant communities such as those from swamp settings from the Parana Forest in northeastern Argentina, is reported from the Jurassic La Matilde Formation (Argentina) by García Massini et al. (2025).[42]
  • Silva et al. (2025) study the taphonomy of exceptionally preserved plant remains from the Upper Cretaceous Santa Marta Formation (Antarctica).[43]
  • Evidence from the study of phytoliths from the Lunpola Basin of the Qinghai–Tibetan Plateau, interpreted as indicative of presence mixed coniferous and broad-leaved forest during the late Oligocene–Early Miocene, is presented by Zhang et al. (2025).[44]
  • A study on the timing of the uplift of the Lhasa and Qiangtang terranes, based on composition of fossil plant communities from the Qinghai–Tibet Plateau (China), is published by Lai et al. (2025).[45]
  • A study on ancient DNA from sediment cores from lakes in Alaska and Siberia, providing evidence of plant extinctions associated with environmental changes during the Pleistocene–Holocene transition, is published by Courtin et al. (2025).[46]
  • El-Saadawi et al. (2025) present an annotated catalog of plant macrofossil remains from Egypt, including fossils ranging from Devonian to Quaternary.[47]

References

[edit]
  1. ^ Schlagintweit, F.; Xu, Y.; Zhang, S. (2025). "Calcareous green algae (Dasycladales, Halimedaceae) from the Upper Cretaceous of the western Tarim Basin, NW China: Systematic palaeontology, microfacies, and palaeobiogeographic significance". Carnets Geol. 25 (4): 89–108. doi:10.2110/carnets.2025.2504.
  2. ^ Wang, J.-J.; Gong, E.-P.; Zhang, Y.-L.; Huang, W.-T.; Li, X.; Wang, L.-F.; Lai, G.-M.; Li, D.-P. (2025). "The role of algal reproduction in phylloid algal buildups: A case study in Pennsylvanian Phylloid algae in southern Guizhou, China". Journal of Palaeogeography. doi:10.1016/j.jop.2025.02.002.
  3. ^ a b Feldberg, K.; Kaasalainen, U.; Mamontov, Y. S.; Gradstein, S. R.; Schäfer-Verwimp, A.; Divakar, P. K.; Schmidt, A. R. (2025). "Extending the fossil record of Miocene neotropical epiphyte communities". Fossil Record. 28 (1): 79–102. doi:10.3897/fr.28.137758.
  4. ^ a b Paulsen, M.; Ohlsen, D.; Cantrill, D. J.; Stilwell, J. (2025). "Eocene liverwort and moss species preserved in Anglesea amber from Australia". Review of Palaeobotany and Palynology. 105330. doi:10.1016/j.revpalbo.2025.105330.
  5. ^ López-García, A. G.; Schmidt, A. R.; Serguera, M.; Regalado, L. (2025). "First record of Selaginella from Miocene amber". Fossil Record. 28 (1): 57–66. doi:10.3897/fr.28.e138310.
  6. ^ Huang, P.; Wang, J.-S.; Wang, Y.-L.; Liu, L.; Zhao, J.-Y.; Xue, J.-Z. (2025). "The smallest Zosterophyllum plant from the Lower Devonian of South China and the divergent life-history strategies in zosterophyllopsids". Proceedings of the Royal Society B: Biological Sciences. 292 (2038). 20242337. doi:10.1098/rspb.2024.2337. PMC 11732410. PMID 39809313.
  7. ^ Li, F.-Y.; Tan, X.; Xiu, Y.-Y.; Liu, W.-T.; Chen, M.-Y.; Tian, N. (2025). "Study on macro- and sporemorphology of a new species of Coniopteris (Dicksoniaceae) from the Middle Jurassic of western Liaoning, Northeast China". Review of Palaeobotany and Palynology. 105312. doi:10.1016/j.revpalbo.2025.105312.
  8. ^ Li, C.X.; Meng, F.W. (2025). "A New Species of Krameropteris (Dennstaedtiaceae) from Mid-Cretaceous Myanmar Amber". Taxonomy. 5 (1). 3. doi:10.3390/taxonomy5010003.
  9. ^ Song, Z.-H.; Wang, Z.-E.; Cao, R.; Wang, Z.-S.; Wang, H.; Chen, G.-H.; Wu, J.-Y. (2025). "Fossil wood of Pinus from the Pliocene of western Yunnan, China and its palaeoclimatic implications". Review of Palaeobotany and Palynology. 334. 105279. doi:10.1016/j.revpalbo.2024.105279.
  10. ^ Akkemik, Ü.; Mantzouka, D. (2025). "A review of the Early Miocene Pinuxylon species of Türkiye with a new species". Turkish Journal of Botany. 49 (1): 52–63. doi:10.55730/1300-008X.2841.
  11. ^ Conceição, D. M.; Esperança Júnior, M. G. F.; Gobo, W. V.; Iannuzzi, R.; Batista, M. E. P.; Nascimento Jr., D. R.; Silva Filho, W. F.; Horodysk, R. S.; Bamford, M. K.; Kunzmann, L. (2025). "Unique conifer assemblage from Late Jurassic-Early Cretaceous deposits (NE Brazil) unveils the paleoclimate and paleobiogeography in the interior of equatorial Gondwana". Cretaceous Research. 106099. doi:10.1016/j.cretres.2025.106099.
  12. ^ Li, P.; Deng, M.; Hou, C.; Xing, Y. (2025). "A new Ephedra macrofossil from the Early Cretaceous Yixian Formation, Liaoning Province, China and its evolutionary significance". Review of Palaeobotany and Palynology. 105314. doi:10.1016/j.revpalbo.2025.105314.
  13. ^ Khan, M. A.; Spicer, R. A.; Su, T.; Roy, K. (2025). "A tropical rainforest biome once existed in India at the K-Pg: Evidence from 'one-vessel' arecoid palms". Review of Palaeobotany and Palynology. 105316. doi:10.1016/j.revpalbo.2025.105316.
  14. ^ Siver, P. A.; Reyes, A. V.; Pisera, A.; Buryak, S.; Wolfe, A. P. (2025). "Palm phytoliths in subarctic Canada imply ice-free winters 48 million years ago during the late early Eocene". Annals of Botany. doi:10.1093/aob/mcaf021. PMID 39928565.
  15. ^ Kumar, S.; Manchester, S. R.; Khan, M. A. (2024). "Oldest menispermaceous endocarp fossil from the Deccan Intertrappean Beds of Central India and its biogeographic implications". Review of Palaeobotany and Palynology. 334. 105249. doi:10.1016/j.revpalbo.2024.105249.
  16. ^ Carpenter, R. J.; McLoughlin, S. (2025). "A new leaf species of Proteaceae and other Gondwanan elements from the early Paleogene Lota–Coronel flora of south–central Chile". Australian Systematic Botany. doi:10.1071/SB24033.
  17. ^ Pan, A. D.; Jacobs, B. F.; Currano, E. D.; Gostel, M. R.; Lowry, P. P.; Plunkett, G. M.; Hoffmann, J.; Geier, C.; Grímsson, F. (2025). "Fossil Astropanax Seem. (Araliaceae) from the early Miocene (21.73 Mya) Mush Valley plant assemblages of Ethiopia". Botanical Journal of the Linnean Society. doi:10.1093/botlinnean/boaf011.
  18. ^ Hung, N. B.; Huang, J.; Del Rio, C.; Hoa, N. T. M.; Truong, D. V.; Pha, P. D.; Su, T.; Li, S.-F. (2025). "First endocarp record of Miquelia (Icacinaceae) from the late Miocene of northern Vietnam and its phytogeographical and paleoecological implications". Review of Palaeobotany and Palynology. 105285. doi:10.1016/j.revpalbo.2025.105285.
  19. ^ Zhao, Y.-S.; Wang, T.-X.; Xiao, S.-M.; Li, S.-F.; Huang, J. (2025). "Fossil pods of tropical tree Peltophorum (Caesalpinioideae, Fabaceae) from southwestern China". Review of Palaeobotany and Palynology. 105282. doi:10.1016/j.revpalbo.2025.105282.
  20. ^ Cao, Z.-D.; Xie, S.-P.; Liu, L.-M.; Li, X.-M.; Zhang, S.-H.; Zhang, Y.-H.; Yan, D.-F. (2025). "A moderate elevation and warm-humid climate of the Wulan Basin, NE Tibetan Plateau in the Middle Miocene indicated by Pueraria macrofossils". Journal of Palaeogeography. doi:10.1016/j.jop.2024.08.012.
  21. ^ Hazra, T.; Khan, M. A. (2025). "Late Neogene diversity of Fabaceae in the Chotanagpur Plateau, eastern India: palaeoecological implications". Earth History and Biodiversity. doi:10.1016/j.hisbio.2025.100020.
  22. ^ Monje Dussán, C.; Pederneiras, L. C.; Angyalossy, V. (2025). "Inferring the hemiepiphytic habit of Ficus (Moraceae) through wood anatomical characters in modern and fossil woods". Brazilian Journal of Botany. doi:10.1007/s40415-025-01067-6.
  23. ^ Zolina, A. A.; Golovneva, L. B.; Grabovskiy, A. A. (2025). "The morphological diversity and distribution of the genus Menispermites (Magnoliopsida) in the Cretaceous of Northern Asia". Palaeontologia Electronica. 28 (1). 28.1.a9. doi:10.26879/1441.
  24. ^ Ma, X.; Zhang, C.; Yang, L.; Hedges, S. B.; Zhong, B. (2025). "New insights on angiosperm crown age based on Bayesian node dating and skyline fossilized birth-death approaches". Nature Communications. 16. 2265. doi:10.1038/s41467-025-57687-9.
  25. ^ Doughty, C. E.; Wiebe, B. C.; Keany, J. M.; Gaillard, C.; Abraham, A. J.; Kristensen, J. A. (2025). "Ecosystem engineers alter the evolution of seed size by impacting fertility and the understory light environment". Palaeontology. 68 (1). e70002. doi:10.1111/pala.70002.
  26. ^ Jiang, Z.; Tian, N.; Wang, Y.; Li, F.; Pei, J.; Uhl, D.; Li, Y.; Wu, H.; Ning, Z.; Hao, R. (2025). "A new exceptionally preserved corystosperm wood from the Jurassic of East Asia". Science China Earth Sciences. 68 (3): 803–810. doi:10.1007/s11430-024-1480-6.
  27. ^ Šimůnek, Z.; Haldovský, J. (2025). "New callistophytalean species from the Duckmantian of the Kladno-Rakovník Basin, Czech Republic". Review of Palaeobotany and Palynology. 105283. doi:10.1016/j.revpalbo.2025.105283.
  28. ^ Correia, P.; Góis-Marques, C. A. (2025). "Palaeopteridium andrenelii sp. nov., a new noeggerathialean species from the Middle Pennsylvanian of Portugal with new insights on the Noeggerathiales". Geological Magazine. 162. e1. doi:10.1017/S0016756824000438.
  29. ^ Wang, K.; Jia, G.; Dong, L.; Wang, J.; Wang, S.; Wang, J.; Wan, M. (2025). "Shanxioxylon yangquanense sp. nov., a new Kasimovian cordaitalean axis from the Benxi Formation (Pennsylvanian, Carboniferous) of Yangquan City, Shanxi Province, North China". Review of Palaeobotany and Palynology. 105287. doi:10.1016/j.revpalbo.2025.105287.
  30. ^ Wang, X.; Lei, Y.; Fu, Q. (2025). "Yuzhoua juvenilis: Another Angiosperm Seen in the Early Permian?". Life. 15 (2). 286. doi:10.3390/life15020286. PMC 11856813.
  31. ^ Greenwood, D. R.; Conran, J. G.; West, C. K. (2025). "A Cycas L. (Cycadaceae) Leaf from the Miocene of Northern South Australia". International Journal of Plant Sciences. 186 (2): 114–126. doi:10.1086/733819.
  32. ^ a b DeBenedetti, F.; Zamaloa, M. C.; Gandolfo, M. A.; Cúneo, N. R.; Fensome, R. A.; Gravendyck, J. (2025). "Nomenclatural and taxonomic notes on the fossil pollen genus Sparganiaceaepollenites Thiergart 1937". Palynology. doi:10.1080/01916122.2025.2463407.
  33. ^ a b Strother, P.; Vecoli, M.; Cesari, C.; Wellman, C. H. (2025). "A freshwater palynological assemblage from the Hirnantian of Saudi Arabia". Review of Palaeobotany and Palynology. 105322. doi:10.1016/j.revpalbo.2025.105322.
  34. ^ Nhamutole, N.; Bamford, M.; Souza, P. A.; Félix, C. M.; Carmo, D. A.; Zimba, A.; Bande, P. (2025). "New palynological data from Maniamba Basin, Mozambique (Karoo): Correlations and implications for Lopingian floristic ecosystem reconstruction". Review of Palaeobotany and Palynology. 105310. doi:10.1016/j.revpalbo.2025.105310.
  35. ^ Li, J.-H.; Peng, J.-G.; Slater, S. M.; Vajda, V. (2025). "Palynofloras across the Triassic–Jurassic boundary on Qinghai-Tibetan Plateau, Southwest China". Palaeoworld. doi:10.1016/j.palwor.2025.200910.
  36. ^ Rodríguez-Barreiro, I.; Santos, A. A.; Villanueva-Amadoz, U.; Hernández, J. M.; McLoughlin, S.; Diez, J. B. (2025). "Angiosperm radiation, diversification, and vegetation shifts through the Albian–Cenomanian of the northern Iberian Peninsula: Palynological evidence from the Las Loras UNESCO Global Geopark". Cretaceous Research. 106086. doi:10.1016/j.cretres.2025.106086.
  37. ^ Abdelhalim, L. A.; Mansour, A.; Tahoun, S. S.; Abdelrahman, K.; Wagreich, M. (2025). "Paleoenvironmental and paleoclimatic trends during the early-middle Cenomanian in northeastern Africa (Egypt): Insights from palynomorph and palynofacies analyses". Review of Palaeobotany and Palynology. 105297. doi:10.1016/j.revpalbo.2025.105297.
  38. ^ Rull, V. (2025). "A critical evaluation of fossil pollen records from the mangrove tree Pelliciera beyond the Neotropics: Biogeographical and evolutionary implications". Review of Palaeobotany and Palynology. 105299. doi:10.1016/j.revpalbo.2025.105299.
  39. ^ Xie, G.; Li, J.-F.; Yao, Y.-F.; Wang, S.-Q.; Sun, B.; Ferguson, D. K.; Li, C.-S.; Li, M.; Deng, T.; Wang, Y.-F. (2025). "Palynological evidence reveals vegetation succession in the central Qinghai-Tibet Plateau during the Late Oligocene to Early Miocene". Journal of Systematics and Evolution. 63 (1): 53–61. doi:10.1111/jse.13168.
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