Skip to main content Skip to main navigation menu Skip to site footer
Type: Article
Published: 2021-06-30
Page range: 14–71
Abstract views: 1469
PDF downloaded: 657

Checklist of fossil liverworts suitable for calibrating phylogenetic reconstructions

Department of Geobiology, University of Göttingen, Goldschmidtstraße 3, 37077 Göttingen, Germany
Department of Systematics, Biodiversity and Evolution of Plants, Albrecht von Haller Institute for Plant Sciences, University of Göttingen, 37073 Göttingen, Germany; Muséum National d’Histoire Naturelle, Institute de Systematique, Évolution, Biodiversité (UMR 7205), 75005 Paris, France
Amber Study Group, c/o Geological-Palaeontological Institute and Museum (CeNak) of the University of Hamburg, Bundesstraße 55, 20146 Hamburg, Germany
Department of Biology I, Systematic Botany and Mycology, Geobio-Center, University of Munich (LMU), Menzinger Straße 67, 80638 Munich, Germany
Gantz Family Collections Center, Science & Education, Field Museum, 1400 South Lake Shore Drive, Chicago, IL 60605-2496, USA
Tsitsin Main Botanical Garden, Russian Academy of Sciences, Moscow, 127276 Russia
Royal Botanic Gardens and Domain Trust, Mrs Macquaries Road, Sydney, NSW 2000, Australia
Department of Geobiology, University of Göttingen, Goldschmidtstraße 3, 37077 Göttingen, Germany
Mittlere Letten 11, 88634 Herdwangen-Schönach, Germany
Department of Biology, Faculty of Science, Burapha University, 169, Long-Hard Bangsaen Road, Mueang, 20131, Chonburi, Thailand
Department of Geobiology, University of Göttingen, Goldschmidtstraße 3, 37077 Göttingen, Germany
Amber Cenozoic Cretaceous divergence time estimates fossil bryophytes leafy liverworts molecular paleontology

Abstract

The number of available liverwort fossils substantially increased within the past decade, which is mainly due to new findings from Cretaceous and Cenozoic amber deposits. Many of them, however, are fragmentary and not predestined for consideration in evolutionary analyses. Here, we list those liverwort fossils that we suggest as suitable for calibrating phylogenetic reconstructions, along with brief descriptions, justification of their use, and age information. Our recommendations are based on thorough microscopic investigation of available fossils from worldwide amber collections including recent findings. We recommend that the following 42 fossil taxa can be used as confident minimum age constraints in phylogenetic reconstructions: Acrolejeunea ucrainica (35 Ma), Anastrophyllum rovnoi (35 Ma), Bazzania polyodus (34 Ma), Blepharolejeunea obovata (15 Ma), the genus Bryopteris with B. bispinosa and B. succinea (15 Ma), Calypogeia stenzeliana (34 Ma), Cephaloziella nadezhdae (35 Ma), the genus Ceratolejeunea with C. antiqua, C. palaeomexicana, and C. sublaetefusca (15 Ma), Cheilolejeunea latiloba (34 Ma), Cheirorhiza brittae (158 Ma), Cololejeunea sp. (15 Ma), Cyclolejeunea archaica (15 Ma), Dibrachiella grollei (15 Ma), Diettertia montanensis (112 Ma), Drepanolejeunea eogena (15 Ma), the genus Frullania with F. baerlocheri, F. cretacea, and F. partita (99 Ma), Frullania subgen. Frullania with F. casparyi (34 Ma) and F. riclefgrollei (35 Ma), F. subgen. Trachycolea with F. rovnoi (35 Ma) and F. schumannii (34 Ma), Gackstroemia cretacea (99 Ma), Geocalyx heinrichsii (34 Ma), the genus Lejeunea with L. hamatiloba, L. miocenica, L. resinata, and L. urbanioides (15 Ma), Lopholejeunea subnigricans (15 Ma), Marchantites cyathodoides (228 Ma), Marchesinia brachiata (15 Ma), Metzgeriothallus sharonae (383 Ma), Microlejeunea nyiahae (52 Ma), Neurolejeunea macrostipula (15 Ma), Nipponolejeunea europaea (34 Ma), Notoscyphus balticus (34 Ma), Odontoschisma (sect. Iwatsukia) dimorpha (34 Ma), Plagiochila groehnii (34 Ma), Porella subgrandiloba (34 Ma), Protolophozia kutscheri (34 Ma), Radula (subgen. Odontoradula) cretacea (99 Ma), R. (subgen. Amentuloradula) heinrichsii (99 Ma), Scapania hoffeinsiana (34 Ma), Solenostoma berendtii (34 Ma), Spruceanthus polonicus (34 Ma), Stictolejeunea squamata (15 Ma), Tetralophozia groehnii (34 Ma), Thysananthus auriculatus (15 Ma), Thysananthus contortus (34 Ma). Furthermore, we transfer Lophozia kutscheri to Protolophozia, Archilejeunea grollei to Dibrachiella, Frullania ucrainica to Acrolejeunea, and Mastigolejeunea extincta to Spruceanthus, based on new fossil evidence and morphological revisions.

Downloads

Download data is not yet available.

References

  1. Arcila, D., Pyron, R.A., Tyler, J.C., Ortí, G. & Betancur, R.R. (2015) An evaluation of fossil tip-dating versus node-age calibrations in tetraodontiform fishes (Teleostei: Percomorphaceae). Molecular Phylogenetics and Evolution 82: 131–145. https://doi.org/10.1016/j.ympev.2014.10.011

  2. Ahonen, I. (2006) The taxonomic position of the genus Nipponolejeunea Hatt. Journal of the Hattori Botanical Laboratory 99: 319–342.

  3. Amakawa, T. (1960) Family Jungermanniaceae of Japan, II. Journal of the Hattori Botanical Laboratory 22: 1–90.

  4. Anderson, H.M. (1976) A review of the Bryophyta from the Upper Triassic Molteno Formation, Karroo Basin, South Africa. Palaeontologia Africana 19: 21–30.

  5. Aranda, S.C., Gradstein, S.R., Patiño, J., Laenen, B., Désamoré, A. & Vanderpoorten, A. (2014) Phylogeny, classification and species delimitation in the liverwort genus Odontoschisma (Cephaloziaceae). Taxon 63: 1008–1025. https://doi.org/10.12705/635.12

  6. Arnell, H.W. (1902) Novae species generis Kantiae. Revue Bryologique 29: 26–32.

  7. Arnell, S.W. (1962) Contribution to the knowledge of the hepaticae of Ecuador. Svensk Botanisk Tidskrift 56: 334–350.

  8. Atwood, J.J. & Mamontov, Y.S. (2020) Notes on Frullania chilcootiensis (Frullaniaceae, Marchantiophyta) with a new synonym, lectotypification and an expanded distribution. Botanica Pacifica 9: 191–195. https://doi.org/10.17581/bp.2020.09212

  9. Austin, C.F. (1876) Notes on hepaticology. Botanical Bulletin. Hanover 1: 35–36. https://doi.org/10.1086/botabull.1.8.2995130

  10. Bakalin, V.A. (2005) Monograficheskaia obrabotka roda Lophozia (Dumort.) Dumort. s. str. [Monograph of the genus Lophozia (Dumort.) Dumort. s. str.]. Nauka, Moscow, 240 pp.

  11. Bakalin, V.A. (2016) A revision of Lepidoziaceae (Hepaticae) in the Russian Far East I. Bazzania. Botanica Pacifica 5: 33–52. https://doi.org/10.17581/bp.2016.05108

  12. Bakalin, V.A. & Vilnet, A.A. (2019) Lophozia fuscovirens sp. nov. (Lophoziaceae, Marchantiophyta): the second taxon with brown gemmae within Lophozia s.s. Nordic Journal of Botany 37: e02294. https://doi.org/10.1111/njb.02294

  13. Barba-Montoya, J., dos Reis, M. & Yang, Z. (2017) Comparison of different strategies for using fossil calibrations to generate the time prior in Bayesian molecular clock dating. Molecular Phylogenetics and Evolution 114: 386–400. https://doi.org/10.1016/j.ympev.2017.07.005

  14. Barthel, M. & Hetzer, H. (1982) Bernstein-Inklusen aus dem Miozän des Bitterfelder Raumes. Zeitschrift für Angewandte Geologie 28: 314–336.

  15. Bastos C.J.P. & Gradstein S.R. (2020) The genus Cheilolejeunea (Marchantiophyta: Lejeuneaceae) in tropical America. Nova Hedwigia 111: 287–335. https://doi.org/10.1127/nova_hedwigia/2020/0596

  16. Beavan, A.J.S., Donoghue, P.C.J., Beaumont, M.A. & Pisani, D. (2020) Performance of a priori and a posteriori calibration strategies in divergence time estimation. Genome Biology and Evolution 12: 1087–1098. https://doi.org/10.1093/gbe/evaa105

  17. Bechteler, J., Lee, G.E., Schäfer-Verwimp, A., Pócs, T., Peralta, D.F., Renner, M.A.M., Schneider, H. & Heinrichs, J. (2016) Towards a monophyletic classification of Lejeuneaceae IV: reinstatement of Allorgella, transfer of Microlejeunea aphanella to Vitalianthus and refinements of the subtribal classification. Plant Systematics and Evolution 302: 187–201. https://doi.org/10.1007/s00606-015-1252-8

  18. Bechteler, J., Schäfer-Verwimp, A., Lee, G.E., Feldberg, K., Pérez-Escobar, O.A., Pócs, T., Peralta, D.F., Renner, M.A.M. & Heinrichs, J. (2017a) Geographical structure, narrow species ranges, and Cenozoic diversification in a pantropical clade of epiphyllous leafy liverworts. Ecology and Evolution 7: 638–653. https://doi.org/10.1002/ece3.2656

  19. Bechteler, J., Schmidt, A.R., Renner, M.A.M., Wang, B., Pérez-Escobar, O.A., Schäfer-Verwimp, A., Feldberg, K. & Heinrichs, J. (2017b) A Burmese amber fossil of Radula (Porellales, Jungermanniopsida) provides insights into the Cretaceous evolution of epiphytic lineages of leafy liverworts. Fossil Record 20: 201–213. https://doi.org/10.5194/fr-20-201-2017

  20. Berry, E.W. (1919) Upper Cretaceous floras of the eastern Gulf region in Tennessee, Mississippi, Alabama, and Georgia. United States Geological Survey, Professional Paper 112: 1–177. https://doi.org/10.3133/pp112

  21. Bischler, H., Bonner, C.E.B. & Miller, H.A. (1963) Studies in Lejeuneaceae VI. The genus Microlejeunea Steph. in Central and South America. Nova Hedwigia 5: 359–411 (plates 59–70).

  22. Bouckaert, R., Heled, J., Kühnert, D., Vaughan, T., Wu, C.-H., Xi, D., Suchard, M.A., Rambaut, A. & Drummond, A.J. (2014) BEAST 2: a software platform for Bayesian evolutionary analysis. PloS Computational Biology 10: e1003537. https://doi.org/10.1371/journal.pcbi.1003537

  23. Braggins, J.E., Renner, M.A.M. & de Lange, P.J. (2014) Additions to the liverwort flora of the Kermadec Islands, New Zealand Botanical Region. Telopea 17: 183–194. https://doi.org/10.7751/telopea20147709

  24. Bromham, L., Duchêne, S., Hua, X., Ritchie, A.M., Duchêne, D.A. & Ho, S.Y.W. (2018) Bayesian molecular dating: opening up the black box. Biological Reviews 93: 1165–1191. https://doi.org/10.1111/brv.12390

  25. Brongniart, A.T. (1849) Végétaux fossiles. In: D’Orbigny, C. (Ed.) Dictionnaire universel d’histoire naturelle. Tome treiziéme. Mm. Renard, Martinet et C., Paris, pp. 52–173.

  26. Brown, E.A. & Pócs, T. (2001) A new species of Radula sect. Cavifolium (Radulaceae: Hepaticae) from Queensland, Australia. Telopea 9: 435–438. https://doi.org/10.7751/telopea20024000

  27. Brown, J.T. & Robison, C.R. (1974) Diettertia montanensis, gen. et sp. nov., a fossil moss from the Lower Cretaceous Kootenai Formation of Montana. Botanical Gazette 135: 170–173. https://doi.org/10.1086/336747

  28. Buch, H. (1928) Die Scapanien Nordeuropas und Sibiriens. II. Systematischer Teil. Societas Scientiarum Fennica. Commentationes Biologicae 3: 1–177.

  29. Buch, H. (1932) Vorarbeiten zu einer Lebermoosflora Fenno-scandias. I. Ein Versuch zur Aufspaltung der Gattungen Lophozia Dum. und Sphenolobus Steph. Memoranda Societatis pro Fauna et Flora Fennica 8: 282–297.

  30. Buch, H. & Persson, H. (1941) Bryophyten von den Azoren und Madeira. Akademische Buchhandlung, Helsingfors, 16 pp.

  31. Buczkowska, K., Bakalin, V., Bączkiewicz, A., Aguero, B., Gonera, P., Ślipiko, M., Szczecińska, M. & Sawicki, J. (2018) Does Calypogeia azurea (Calypogeiaceae, Marchantiophyta) occur outside Europe? Molecular and morphological evidence. PloS ONE 13: e0204561. https://doi.org/10.1371/journal.pone.0204561

  32. Carruthers, T. & Scotland, R.W. (2020) Insights from empirical analyses and simulations on using multiple fossil calibrations with relaxed clocks to estimate divergence times. Molecular Biology and Evolution 37: 1508–1529. https://doi.org/10.1093/molbev/msz310

  33. Carter, B.E., Larraín, J., Manukjanová, A., Shaw, B., Shaw, A.J., Heinrichs, J., de Lange, P., Suleiman, M., Thouvenot, L. & von Konrat, M. (2017) Species delimitation and biogeography of a southern hemisphere liverwort clade, Frullania subgenus Microfrullania (Frullaniaceae, Marchantiophyta). Molecular Phylogenetics and Evolution 107: 16–26. https://doi.org/10.1016/j.ympev.2016.10.002

  34. Caspary, R. (1887) Einige neue Pflanzenreste aus dem samländischen Bernstein. Schriften der Physikalisch-Ökonomischen Gesellschaft zu Königsberg (Abhandlungen) 27: 1–8 [209]. Tafel I. „1886“.

  35. Caspary, R. & Klebs, R. (1907) Die Flora des Bernsteins und anderer fossiler Harze des ostpreußischen Tertiärs. Abhandlungen der Königlich Preussischen Geologischen Landesanstalt, N. F. 4: 1–182. Text + Atlas.

  36. Cheah, Y.-H. & Yong, K.-T. (2016) New records of Bazzania species (Marchantiophyta: Lepidoziaceae) in peninsula Malaysia with identification key. Cryptogamie, Bryologie 37: 199–210. https://doi.org/10.7872/cryb/v37.iss2.2016.199

  37. Choi, S.S., Bakalin, V.A. & Sun, B.-Y. (2012) Scapania and Macrodiplophyllum in the Russian Far East. Botanica Pacifica 1: 31–95. https://doi.org/10.17581/bp.2012.01104

  38. Cooper, E.D., Henwood, M.J. & Brown, E.A. (2012) Are the liverworts really that old? Cretaceous origins and Cenozoic diversifications in Lepidoziaceae reflect a recurrent theme in liverwort evolution. Biological Journal of the Linnean Society 107: 425–441. https://doi.org/10.1111/j.1095-8312.2012.01946.x

  39. Crandall-Stotler, B., Stotler, R.E. & Long, D.G. (2009) Phylogeny and classification of the Marchantiophyta. Edinburgh Journal of Botany 66: 155–198. https://doi.org/10.1017/S0960428609005393

  40. Dauphin, G. (2003) Ceratolejeunea. Flora Neotropica Monograph 90: 1–86.

  41. De Roo, R.T., Hedderson, T.A. & Söderström, L. (2007) Molecular insights into the phylogeny of the leafy liverwort family Lophoziaceae Cavers. Taxon 56: 301–314. https://doi.org/10.1002/tax.562005

  42. Devos, N., Renner, M.A.M., Gradstein, S.R., Shaw, J. & Vanderpoorten, A. (2011) Molecular data challenge traditional subgeneric divisions in the leafy liverwort Radula. Taxon 60: 1623–1632. https://doi.org/10.1002/tax.606007

  43. Dickson, J. (1793) Fasciculus tertius plantarum cryptogamicarum britanniae. G. Nichol, London, 24 pp.

  44. Didier, G. & Laurin, M. (2020) Exact distribution of divergence times from fossil ages and tree topologies. Systematic Biology 69: 1068–1087. https://doi.org/10.1093/sysbio/syaa021

  45. Dixon, H.N., Schiffner, V. & Verdoorn, F. (1932) Bryophyta nova (1–5). Annales Bryologici 5: 159–164.

  46. Dong, S., Schäfer-Verwimp, A., Meinecke, P., Feldberg, K., Bombosch, A., Pócs, T., Schmidt, A.R., Reitner, J., Schneider, H. & Heinrichs, J. (2012) Tramps, narrow endemics and morphologically cryptic species in the epiphyllous liverwort Diplasiolejeunea. Molecular Phylogenetics and Evolution 65: 582–594. https://doi.org/10.1016/j.ympev.2012.07.009

  47. Dong, S., Schäfer-Verwimp, A., Pócs, T., Feldberg, K., Czumaj, A., Schmidt, A.R., Schneider, H. & Heinrichs, J. (2013) Size doesn’t matter—recircumscription of Microlejeunea (Lejeuneaceae, Porellales) based on molecular and morphological evidence. Phytotaxa 85 (2): 41–55. https://doi.org/10.11646/phytotaxa.85.2.2

  48. Douin, C. (1920) La famille des Céphaloziellacées. Mémoires de la Société Botanique de France 29: 1–90. https://doi.org/10.1080/00378941.1916.10839749

  49. Drummond, A.J. & Bouckaert, R.R. (2015) Bayesian evolutionary analysis with BEAST. Cambridge University Press, Cambridge, 260 pp. https://doi.org/10.1017/CBO9781139095112

  50. Dumortier, B.C.J. (1822) Commentationes botanicae. Ch. Casterman-Dieu, Tournay, 117 pp. https://doi.org/10.5962/bhl.title.10534

  51. Dumortier, B.C.J. (1835) Recueil d‘Observations sur les Jungermanniacées. I. Révision des genres. J.-A. Blanquart, Tournay, 27 pp. https://doi.org/10.5962/bhl.title.731

  52. Dunlop, J.A. (2010) Bitterfeld amber. In: Penney, D. (Ed.) Biodiversity of fossils in amber from the major world deposits. Siri Scientific Press, Manchester, pp. 57–68.

  53. Edwards, D., Morris, J.L., Richardson, J.B. & Kenrick, P. (2014) Cryptospores and cryptophytes reveal hidden diversity in early land floras. New Phytologist 202: 50–78. https://doi.org/10.1111/nph.12645

  54. Evans, A.W. (1904) Hepaticae of Puerto Rico. IV. Odontolejeunea, Cyclolejeunea and Prionolejeunea. Bulletin of the Torrey Botanical Club 31: 183–226. https://doi.org/10.2307/2478687

  55. Evans, A.W. (1907) Hepaticae of Puerto Rico. VII. Stictolejeunea, Neurolejeunea, Omphalanthus, and Lopholejeunea. Bulletin of the Torrey Botanical Club 34: 1–34. https://doi.org/10.2307/2479163

  56. Feldberg, K., Heinrichs, J., Schmidt, A.R., Váňa, J. & Schneider, H. (2013) Exploring the impact of fossil constraints on the divergence time estimates of derived liverworts. Plant Systematics and Evolution 299: 585–601. https://doi.org/10.1007/s00606-012-0745-y

  57. Feldberg, K., Schneider, H., Stadler, T., Schäfer-Verwimp, A., Schmidt, A.R. & Heinrichs, J. (2014) Epiphytic leafy liverworts diversified in angiosperm-dominated forests. Scientific Reports 4: 5974. https://doi.org/10.1038/srep05974

  58. Feldberg, K., Váňa, J., Krusche, J., Kretschmann, J., Patzak, S.D.F., Pérez-Escobar, O.A., Rudolf, N.R., Seefelder, N., Schäfer-Verwimp, A., Long, D.G., Schneider, H. & Heinrichs, J. (2016) A phylogeny of Cephaloziaceae (Jungermanniopsida) based on nuclear and chloroplast DNA markers. Organisms Diversity and Evolution 16: 727–742. https://doi.org/10.1007/s13127-016-0284-4

  59. Feldberg, K., Váňa, J., Schäfer-Verwimp, A., Krings, M., Gröhn, C., Schmidt, A.R. & Heinrichs, J. (2017) Problems related to the taxonomic placement of incompletely preserved amber fossils: transfer of the Paleogene liverwort Cylindrocolea dimorpha (Cephaloziellaceae) to the extant Odontoschisma sect. Iwatsukia (Cephaloziaceae). Fossil Record 20: 147–157. https://doi.org/10.5194/fr-20-147-2017

  60. Feldberg, K., Müller, A.S., Schäfer-Verwimp, A., von Konrat, M., Schmidt, A.R. & Heinrichs, J. (2018) Frullania grabenhorstii sp. nov., a fossil liverwort (Jungermanniopsida: Frullaniaceae) with perianth from Bitterfeld amber. Bryophyte Diversity and Evolution 40: 91–103. https://doi.org/10.11646/bde.40.2.7

  61. Feldberg, K., Schäfer-Verwimp, A., Renner, M.A.M., von Konrat, M., Bechteler, J., Müller, P., Wang, Y.-D., Schneider, H. & Schmidt, A.R. (2021) Liverworts from Cretaceous amber. Cretaceous Research. [in press]

  62. Frahm, J.-P. & Gröhn, C. (2013) More fossil bryophytes from Baltic amber. Archive for Bryology 159: 1–9.

  63. Godfrey, J.D. & Godfrey, G.A. (1980) Frullania hattoriana, a new hepatic from British Columbia, Canada. Journal of the Hattori Botanical Laboratory 48: 321–327.

  64. Göppert, H.R. (1845) Übersicht der bis jetzt bekannten in und mit dem Bernstein vorkommenden vegetabilischen Reste. In: Berendt, G.C. (Ed.) Die im Bernstein befindlichen organischen Reste der Vorwelt. Erster Band. I. Abteilung. Nicolaische Buchhandlung, Berlin, pp. 69–125. https://doi.org/10.5962/bhl.title.66910

  65. Göppert, H.R. (1853) Über die Bernsteinflora. Verhandlungen der Königlich-Preußischen Akademie der Wissenschaften zu Berlin 1853: 450–476.

  66. Gottsche, C.M. (1857) Pugillus novarum hepaticarum. Annales des Sciences Naturelles; Botanique (sér. 4) 8: 318–348.

  67. Gottsche, C.M. (1886) Über die im Bernstein eingeschlossenen Lebermoose. Botanisches Centralblatt 25: 95–97, 121–123.

  68. Gottsche, C.M., Lindenberg, J.B.W. & Nees, C.G. (1845a) Synopsis hepaticarum, fasc. 2. Meissner, Hamburg, pp. 145–304. https://doi.org/10.5962/bhl.title.15221

  69. Gottsche, C.M., Lindenberg, J.B.W. & Nees, C.G. (1845b) Synopsis hepaticarum, fasc. 3. Meissner, Hamburg, pp. 305–464. https://doi.org/10.5962/bhl.title.15221

  70. Gradstein, S.R. (1975) A taxonomic monograph of the genus Acrolejeunea (Hepaticae). Bryophytorum Bibliotheca 4: 1–162.

  71. Gradstein, S.R. (1993) New fossil Hepaticae preserved in amber of the Dominican Republic. Nova Hedwigia 57: 353–374.

  72. Gradstein, S.R. (1994) Lejeuneaceae: Ptychantheae. Brachiolejeuneae. Flora Neotropica Monograph 62: 1–225.

  73. Gradstein, S.R. (2012) An overview of the genus Marchesinia (Marchantiophyta: Lejeuneaceae), with special attention to the species described from Asia and Oceania. Polish Botanical Journal 57: 69–79.

  74. Gradstein, S. R. (2013) A classification of Lejeuneaceae (Marchantiophyta) based on molecular and morphological evidence. Phytotaxa 100: 6–20. https://doi.org/10.11646/phytotaxa.100.1.2

  75. Gradstein, S.R. (2017) Bazzania (Marchantiophyta) in South America. Nova Hedwigia 105: 243–266. https://doi.org/10.1127/nova_hedwigia/2017/0409

  76. Gradstein, S.R. (2018) Amphi-Pacific tropical disjunctions in the bryophyte floras of Asia and the New World. Philippine Journal of Systematic Biology 12: 1–11. https://doi.org/10.26757/pjsb.2018a12012

  77. Gradstein, S.R. (2020) The genera of Lejeuneaceae (Marchantiophyta) of tropical America–an update. Nova Hedwigia Beiheft 150: 81–96. https://doi.org/10.1127/nova-suppl/2020/081

  78. Gradstein, S.R. & Ilkiu-Borges, A.L. (2015) A taxonomic revision of the genus Odontoschisma (Marchantiophyta: Cephaloziaceae). Nova Hedwigia 100: 15–100. https://doi.org/10.1127/nova_hedwigia/2014/0219

  79. Gradstein, S.R., Churchill, S.P. & Salazar-Allen, N. (2001) Guide to the bryophytes of tropical America. Memoirs of the New York Botanical Garden 86: 1–577.

  80. Gradstein, S.R., Aranda, S.C. & Vanderpoorten, A. (2014) Notes on Early Land Plants Today. 47. Transfer of Iwatsukia to Odontoschisma (Cephaloziaceae, Marchantiophyta). Phytotaxa 162 (4): 232–233. https://doi.org/10.11646/phytotaxa.162.4.6

  81. Gray, S.F. (1821) Natural arrangement of British plants. Vol. 1. Baldwin, Craddock, and Joy, London, 824 pp. https://doi.org/10.5962/bhl.title.43804

  82. Grolle, R. (1970) Radula castlei sp. nov. und Anmerkungen zur Gattung Radula. The Bryologist 73: 662–668. https://doi.org/10.2307/3241278

  83. Grolle, R. (1971) Hepaticopsida. In: Bakker, E.M.v.Z. Sr., Winterbottom, J.M. & Dyer, R.A. (Eds.) Marion and Prince Edward Islands. Report on the South African Biological and Geological Expedition 1965-1966. Balkema, Cape Town, pp. 228–236.

  84. Grolle, R. (1976) Verzeichnis der Lebermoose Europas und benachbarter Gebiete. Feddes Repertorium 87: 171–279. https://doi.org/10.1002/fedr.19760870303

  85. Grolle, R. (1980a) Lebermoose im Bernstein 1. Feddes Repertorium 91: 183–190.

  86. Grolle, R. (1980b) Lebermoose im Bernstein 2. Feddes Repertorium 91: 401–407.

  87. Grolle, R. (1981a) Nipponolejeunea fossil in Europa. Journal of the Hattori Botanical Laboratory 50: 143–157.

  88. Grolle, R. (1981b) Was ist Lejeunea schumannii Caspary aus dem Baltischen Bernstein? Occasional Papers of the Farlow Herbarium of Cryptogamic Botany 16: 101–110.

  89. Grolle, R. (1982) Trocholejeunea fossil in Europa. Journal of the Hattori Botanical Laboratory 51: 175–193.

  90. Grolle, R. (1983) Leucolejeunea antiqua n. sp., das erste Lebermoos aus Dominikanischem Bernstein. Stuttgarter Beiträge zur Naturkunde, Serie B 96: 1–9.

  91. Grolle, R. (1984a) Bryopteris und Cyclolejeunea fossil in Dominikanischem Bernstein. Journal of the Hattori Botanical Laboratory 56: 271–280.

  92. Grolle, R. (1984b) Cyrtolejeunea suzannensis spec. nov., ein weiteres fossiles Lebermoos in Dominikanischem Bernstein. Cryptogamie: Bryologie-Lichénologie 5: 27–32.

  93. Grolle, R. (1984c) Die Lebermoosgattung Cheilolejeunea fossil in Mitteleuropa. Feddes Repertorium 95: 229–236.

  94. Grolle, R. (1984d) Lejeunea palaeomexicana n. sp., das erste Moos aus Mexikanischem Bernstein. Stuttgarter Beiträge zur Naturkunde, Serie B 108: 1–7.

  95. Grolle, R. (1985a) Zwei weitere Lebermoose in Bernstein aus Bitterfeld (DDR). Feddes Repertorium 96: 41–46.

  96. Grolle, R. (1985b) Monograph of Frullania in Baltic amber. Prace Muzeum Ziemi 37: 87–100, pl. I–VI.

  97. Grolle, R. (1985c) Fossil Spruceanthus in Europe and two other hepatics in Baltic amber. Prace Muzeum Ziemi 37: 79–85.

  98. Grolle, R. (1988) Die Lebermoosgattung Notoscyphus fossil in Europa. Feddes Repertorium 99: 561–564 (Plates LXIV and LXV).

  99. Grolle, R. (1989) Weitere Lebermoosfunde in Bitterfelder Bernstein, darunter Radula oblongifolia Caspary mit Sporophyt. Feddes Repertorium 100: 131–136.

  100. Grolle, R. (1993a) Bryopteris bispinosa spec. nov. (Lejeuneaceae), ein weiteres Lebermoos in Dominikanischem Bernstein. Journal of the Hattori Botanical Laboratory 74: 71–76.

  101. Grolle, R. (1993b) Ein autözisches Lebermoos mit Perianth in Dominikanischem Bernstein: Drepanolejeunea eogena spec. nov. Nova Hedwigia 57: 375–380.

  102. Grolle, R. (1998) The Eocene hepatic Frullania baltica found with androecium, perianth and capsule. Nova Hedwigia 66: 451–456. https://doi.org/10.1127/nova.hedwigia/66/1998/451

  103. Grolle, R. (1999) Metacalypogeia (Calypogeiaceae, Hepaticae) new to Europe as Baltic amber fossil. Bryobrothera 5: 87–91.

  104. Grolle, R. (2003) Frullania mammilligera sp. nov., a new Eocene species of Hepaticae found in Bitterfeld Amber of central Germany. Courier Forschungs-Institut Senckenberg 241: 155–161.

  105. Grolle, R. & Braune, W. (1988) Bazzania oleosa, ein Lebermoos mit erhaltenen Ölkörpern in dominikanischem Bernstein. Beiheft zur Nova Hedwigia 90: 101–108.

  106. Grolle, R. & Heinrichs, J. (2003) Eocene Plagiochila groehnii sp. nov.–the first representative of Plagiochilaceae in Baltic amber. Cryptogamie, Bryologie 24: 289–293.

  107. Grolle, R. & Meister, K. (2004a) Lophozia kutscheri, a new hepatic (Jungermanniales) in Bitterfeld amber from Central Germany. The Bryologist 107: 79–81. https://doi.org/10.1639/0007-2745(2004)107[79:LKANHJ]2.0.CO;2

  108. Grolle, R. & Meister, K. (2004b) The liverworts in Baltic and Bitterfeld amber. Weissdorn-Verlag, Jena, 91 pp.

  109. Grolle, R. & Schmidt, A. (2001) A fossil Scapania (Hepaticae) with perianth and capsule in Bitterfeld amber (Eocene) from Germany. The Bryologist 104: 362–366. https://doi.org/10.1639/0007-2745(2001)104[0362:AFSHWP]2.0.CO;2

  110. Grolle, R. & So, M.L. (2004) A fossil Porella (Porellaceae, Hepaticae) in Eocene Baltic amber. Botanical Journal of the Linnean Society 145: 485–488. https://doi.org/10.1111/j.1095-8339.2004.00291.x

  111. Grolle, R., Zhu, R.-L. & Gradstein, S.R. (2001) On Cyrtolejeunea A.Evans (Lejeuneaceae, Hepaticae). Taxon 50: 1067–1074. https://doi.org/10.2307/1224721

  112. Grolle, R., Meister, K. & So, M.L. (2004) New evidence on the taxonomic position of the Eocene Jungermannites contortus (Jungermanniales: Lejeuneaceae). Cryptogamie, Bryologie 25: 117–123.

  113. Guindon, S. (2018) Accounting for calibration uncertainty: Bayesian molecular dating as a “doubly intractable” problem. Systematic Biology 67: 651–661. https://doi.org/10.1093/sysbio/syy003

  114. Hartmann, F.A., Wilson, R., Gradstein, S.R., Schneider, H. & Heinrichs, J. (2006) Testing hypotheses on species delimitations and disjunctions in the liverwort Bryopteris (Jungermanniopsida: Lejeuneaceae). International Journal of Plant Sciences 167: 1205–1214. https://doi.org/10.1086/508023

  115. Hattori, S. (1944) Contributio ad floram hepaticarum austro-kiushiuensem. Bulletin of the Tokyo Science Museum 11: 1–203.

  116. Hattori, S. (1953) Notes on little known Japanese species of Hepaticae (3). Journal of Japanese Botany 28: 231–235.

  117. Hattori, S. (1973) Notes on the Asiatic species of the genus Frullania, Hepaticae. III. Journal of the Hattori Botanical Laboratory 37: 85–120.

  118. Hattori, S. (1974) Notes on the Asiatic species of the genus Frullania, Hepaticae. VI. Journal of the Hattori Botanical Laboratory 38: 223–274.

  119. Hattori, S. (1986) A synopsis of New Caledonian Frullaniaceae. Journal of the Hattori Botanical Laboratory 60: 203–237.

  120. Hattori, S. & Zhang, M.-X. (1985) Porellaceae of Shensi Province, China. Journal of Japanese Botany 60: 321–326.

  121. Heath, T.A., Huelsenbeck, J.P. & Stadler, T. (2014) The fossilized birth–death process for coherent calibration of divergence-time estimates. Proceedings of the National Academy of Sciences of the United States of America 111: E2957–E2966. https://doi.org/10.1073/pnas.1319091111

  122. Heinrichs, J. & Schmidt, A.R. (2010) An inclusion of Frullania subgen. Diastaloba s. l. (Frullaniaceae, Porellales) in Dominican amber. Tropical Bryology 31: 91–94. https://doi.org/10.11646/bde.31.1.15

  123. Heinrichs, J., Hentschel, J., Wilson, R., Feldberg, K. & Schneider, H. (2007) Evolution of leafy liverworts (Jungermanniidae, Marchantiophyta): estimating divergence times from chloroplast DNA sequences using penalized likelihood with integrated fossil evidence. Taxon 56: 31–44.

  124. Heinrichs, J., Klugmann, F., Hentschel, J. & Schneider, H. (2009) DNA taxonomy, cryptic speciation and diversification of the Neotropical-African liverwort, Marchesinia brachiata (Lejeuneaceae, Porellales). Molecular Phylogenetics and Evolution 53: 113–121. https://doi.org/10.1016/j.ympev.2009.05.032

  125. Heinrichs, J., Hentschel, J., Bombosch, A., Fiebig, A., Reise, J., Edelmann, M., Kreier, H.-P., Schäfer-Verwimp, A., Caspari, S., Schmidt, A.R., Zhu, R.-L., von Konrat, M., Shaw, B. & Shaw, A.J. (2010). One species or at least eight? Delimitation and distribution of Frullania tamarisci (L.) Dumort. s. l. (Jungermanniopsida, Porellales) inferred from nuclear and chloroplast DNA markers. Molecular Phylogenetics and Evolution 56: 1105–1114. https://doi.org/10.1016/j.ympev.2010.05.004

  126. Heinrichs, J., Kreier, H.-P., Feldberg, K., Schmidt, A.R., Zhu, R.-L., Shaw, B., Shaw, A.J. & Wissemann, V. (2011a) Formalizing morphologically cryptic biological entities: New insights from DNA taxonomy, hybridization, and biogeography in the leafy liverwort Porella platyphylla (Jungermanniopsida, Porellales). American Journal of Botany 98: 12521262. https://doi.org/10.3732/ajb.1100115

  127. Heinrichs, J., Reiner-Drehwald, M.E., Feldberg, K., Grimaldi, D.A., Nascimbene, P.C., von Konrat, M. & Schmidt, A.R. (2011b) Kaolakia borealis nov. gen. et sp. (Porellales, Jungermanniopsida): A leafy liverwort from the Cretaceous of Alaska. Review of Palaeobotany and Palynology 165: 235–240. https://doi.org/10.1016/j.revpalbo.2011.04.002

  128. Heinrichs, J., Bombosch, A., Feldberg, K., Kreier, H.-P., Hentschel, J., Eckstein, J., Long, D., Zhu, R.-L., Schäfer-Verwimp, A., Schmidt, A.R., Shaw, B., Shaw, A.J. & Váňa, J. (2012a) A phylogeny of the northern temperate leafy liverwort genus Scapania (Scapaniaceae, Jungermanniales). Molecular Phylogenetics and Evolution 62: 973–985. https://doi.org/10.1016/j.ympev.2011.11.029

  129. Heinrichs, J., Reiner-Drehwald, M.E., Feldberg, K., von Konrat, M., Hentschel, J., Váňa, J., Nascimbene, P., Grimaldi, D. & Schmidt, A.R. (2012b) The leafy liverwort Frullania (Jungermanniopsida) in the Cretaceous amber forest of Myanmar. Review of Palaeobotany and Palynology 169: 21–28. https://doi.org/10.1016/j.revpalbo.2011.10.002

  130. Heinrichs, J., von Konrat, M., Grabenhorst, H. & Schmidt, A.R. (2012c) The sporophyte of the Paleogene liverwort Frullania varians Caspary. Fossil Record 15: 115–120. https://doi.org/10.1002/mmng.201200009

  131. Heinrichs, J., Dong, S., Schäfer-Verwimp, A., Pócs, T., Feldberg, K., Czumaj, A., Schmidt, A.R., Reitner, J., Renner, M.A.M., Hentschel, J., Stech, M. & Schneider, H. (2013) Molecular phylogeny of the leafy liverwort Lejeunea (Porellales): evidence for a Neotropical origin, uneven distribution of sexual systems and insufficient taxonomy. PloS ONE 8: e82547. https://doi.org/10.1371/journal.pone.0082547

  132. Heinrichs, J., Schäfer-Verwimp, A., Boxberger, J., Feldberg, K., Solórzano Kraemer, M.M. & Schmidt, A.R. (2014a) A fossil species of Ceratolejeunea (Lejeuneaceae, Porellales) preserved in Miocene Mexican amber. The Bryologist 117: 10–14. https://doi.org/10.1639/0007-2745-117.1.010

  133. Heinrichs, J., Schäfer-Verwimp, A., Feldberg, K. & Schmidt, A.R. (2014b) The extant liverwort Gackstroemia (Lepidolaenaceae, Porellales) in Cretaceous amber from Myanmar. Review of Palaeobotany and Palynology 203: 48–52. https://doi.org/10.1016/j.revpalbo.2014.01.004

  134. Heinrichs, J., Kettunen, E., Lee, G.E., Marzaro, G., Pócs, T., Ragazzi, E., Renner, M.A.M., Rikkinen, J., Sass-Gyarmati, A., Schäfer-Verwimp, A., Scheben, A., Solórzano Kraemer, M.M., Svojtka, M. & Schmidt, A.R. (2015a) Lejeuneaceae (Marchantiophyta) from a species-rich taphocoenosis in Miocene Mexican amber, with a review of liverworts fossilised in amber. Review of Palaeobotany and Palynology 221: 59–70. https://doi.org/10.1016/j.revpalbo.2015.05.007

  135. Heinrichs, J., Scheben, A., Lee, G.E., Váňa, J., Schäfer-Verwimp, A., Krings, M. & Schmidt, A.R. (2015b) Molecular and morphological evidence challenges the records of the extant liverwort Ptilidium pulcherrimum in Eocene Baltic amber. PloS ONE 10: e0140977. https://doi.org/10.1371/journal.pone.0140977

  136. Heinrichs, J., Schmidt, A.R., Schäfer-Verwimp, A., Gröhn, C. & Renner, M.A.M. (2015c) The leafy liverwort Notoscyphus balticus sp. nov. (Jungermanniales) in Eocene Baltic amber. Review of Palaeobotany and Palynology 217: 39–44. https://doi.org/10.1016/j.revpalbo.2015.02.006

  137. Heinrichs, J., Scheben, A., Bechteler, J., Lee, G.E., Schäfer-Verwimp, A., Hedenäs, L., Singh, H., Pócs, T., Nascimbene, P.C., Peralta, D.F., Renner, M.A.M. & Schmidt, A.R. (2016a) Crown group Lejeuneaceae and pleurocarpous mosses in early Eocene (Ypresian) Indian amber. PloS ONE 11: e0156301. https://doi.org/10.1371/journal.pone.0156301

  138. Heinrichs, J., Schmidt, A.R., Schäfer-Verwimp, A., Bauerschmidt, L., Neumann, C., Gröhn, C., Krings, M. & Renner, M.A.M. (2016b) Revision of the leafy liverwort genus Radula (Porellales, Jungermanniopsida) in Baltic and Bitterfeld amber. Review of Palaeobotany and Palynology 235: 157–164. https://doi.org/10.1016/j.revpalbo.2016.09.004

  139. Heinrichs, J., Feldberg, K., Bechteler, J., Müller, P., Renner, M.A.M., Váňa, J., Schäfer-Verwimp, A. & Schmidt, A.R. (2017a) A fossil genus of the Frullaniaceae (Porellales, Jungermanniopsida) from the mid-Cretaceous of Myanmar. Cretaceous Research 74: 223–226.        https://doi.org/10.1016/j.cretres.2017.02.023

  140. Heinrichs, J., Feldberg, K., Müller, P., Schäfer-Verwimp, A., von Konrat, M., Ilsemann, B. & Krings, M. (2017b) Frullania pinnata spec. nov. (Frullaniaceae, Porellales), a new leafy liverwort in mid-Cretaceous Burmese amber from Myanmar. Cretaceous Research 78: 56–60. https://doi.org/10.1016/j.cretres.2017.05.030

  141. Heinrichs, J., Feldberg, K., Bechteler, J., Regalado, L., Renner, M.A.M., Schäfer-Verwimp, A., Gröhn, C., Müller, P., Schneider, H. & Krings, M. (2018a) A comprehensive assessment of the fossil record of liverworts in amber. In: Krings, M., Cúneo, N.R., Harper, C.J. & Rothwell, G.W. (eds.) Transformative Paleobotany. Papers to commemorate the life and legacy of Thomas N. Taylor. Elsevier/Academic Press, New York, pp. 213–252. https://doi.org/10.1016/B978-0-12-813012-4.00012-7

  142. Heinrichs, J., Schäfer-Verwimp, A., Renner, M.A.M. & Feldberg, K. (2018b) Cheilolejeunea lamyi sp. nov., a fossil Lejeuneaceae from Miocene Dominican amber. Cryptogamie, Bryologie 39: 155–161. https://doi.org/10.7872/cryb/v39.iss2.2018.155

  143. Hentschel, J., Paton, J.A., Schneider, H. & Heinrichs, J. (2007) Acceptance of Liochlaena Nees and Solenostoma Mitt., the systematic position of Eremonotus Pearson and notes on Jungermannia L. s.l. (Jungermanniidae) based on chloroplast DNA sequence data. Plant Systematics and Evolution 268: 147–157. https://doi.org/10.1007/s00606-007-0549-7

  144. Hentschel, J., Schmidt, A.R. & Heinrichs, J. (2009a) Frullania cretacea, sp. nov. (Porellales, Jungermanniopsida), a leafy liverwort preserved in Cretaceous amber from Myanmar. Cryptogamie, Bryologie 30: 323–328.

  145. Hentschel, J., von Konrat, M.J., Pócs, T., Schäfer-Verwimp, A., Shaw, A.J., Schneider, H. & Heinrichs, J. (2009b) Molecular insights into the phylogeny and subgeneric classification of Frullania Raddi (Frullaniaceae, Porellales). Molecular Phylogenetics and Evolution 52: 142–156. https://doi.org/10.1016/j.ympev.2008.12.021

  146. Hentschel, J., von Konrat, M., Söderström, L., Hagborg, A., Larraín, J., Sukkharak, P., Uribe, J. & Zhang, L. (2015) Notes on Early Land Plants Today. 72. Infrageneric classification and new combinations, new names, new synonyms in Frullania (Marchantiophyta). Phytotaxa 220: 127–142. https://doi.org/10.11646/phytotaxa.220.2.3

  147. Hernick, L.V., Landing, E. & Bartowski, K.E. (2008) Earth’s oldest liverworts—Metzgeriothallus sharonae sp. nov. from the Middle Devonian (Givetian) of eastern New York, USA. Review of Palaeobotany and Palynology 148: 154–162. https://doi.org/10.1016/j.revpalbo.2007.09.002

  148. Hong, W.S. (1990) The family Calypogeiaceae in North America west of the hundredth meridian. The Bryologist 93: 313–318. https://doi.org/10.2307/3243519

  149. Horikawa, Y. (1939) Contributions to the bryological flora of Eastern Asia. VI. Journal of Japanese Botany 15: 359–368.

  150. Hudson, W. (1778) Flora Anglica, ed. 2, tom. 2. J. Nourse, London, pp. 335–690.

  151. Inoue, H. (1959) On Metacalypogeia, a new genus of Hepaticae. Journal of the Hattori Botanical Laboratory 21: 231–235.

  152. Inoue, H. (1978) Anastrophyllum ellipticum Inoue (sp. nov., Hepaticae) from Japan. Bulletin of the National Science Museum, Tokyo. Series B, Botany 4: 13–17.

  153. Iturralde-Vinent, M.A. & MacPhee, R.D.E. (2019) Remarks on the age of Dominican amber. Palaeoentomology 2: 236–240. https://doi.org/10.11646/palaeoentomology.2.3.7

  154. Jack, J.B. & Stephani, F. (1892) Hepaticae Wallisianae. Hedwigia 31: 11–27.

  155. Kaasalainen, U., Heinrichs, J., Renner, M.A.M., Hedenäs, L., Schäfer-Verwimp, A., Lee, G.E., Ignatov, M.S., Rikkinen, J. & Schmidt, A.R. (2017) A Caribbean epiphyte community preserved in Miocene Dominican amber. Earth and Environmental Science Transactions of the Royal Society of Edinburgh 107: 321–331. https://doi.org/10.1017/S175569101700010X

  156. Kachroo, P. (1968) History of the genus Cheilolejeunea. Ceylon Journal of Science. Biological Sciences 8: 1–10.

  157. Kasiński, J.R., Kramarska, R., Słodkowska, B., Sivkov, V. & Piwocki, M. (2020) Paleocene and Eocene deposits on the eastern margin of the Gulf of Gdańsk (Yantarny P-1 borehole, Kaliningrad region, Russia). Geological Quarterly 64: 29–53. https://doi.org/10.7306/gq.1513

  158. Katagiri, T. (2015) First fossil record of the liverwort family Cephaloziaceae (Jungermanniales, Marchantiophyta) from Baltic amber. Nova Hedwigia 101: 347–354. https://doi.org/10.1127/nova_hedwigia/2015/0276

  159. Katagiri, T. (2018) Geocalyx heinrichsii sp. nov., the first representative of Geocalycaceae (Jungermanniales, Marchantiophyta) in Baltic amber. Bryophyte Diversity and Evolution 40: 113–117. https://doi.org/10.11646/bde.40.2.9

  160. Katagiri, T. & Shinden, H. (2020) Discovery of a simple thalloid liverwort Metzgeriites kujiensis (Metzgeriaceae), a new species from Late Cretaceous Japanese amber. Hattoria 11: 13–21. https://doi.org/10.18968/hattoria.11.0_13

  161. Kettunen, E., Sadowski, E.-M., Seyfullah, L.J., Dörfelt, H., Rikkinen, J. & Schmidt, A.R., (2019) Caspary’s fungi from Baltic amber: historic specimens and new evidence. Papers in Palaeontology 5: 365–389. https://doi.org/10.1002/spp2.1238

  162. Kitagawa, N. (1964) A new genus of Hepaticae from North Borneo. Journal of the Hattori Botanical Laboratory 27: 178–182.

  163. Konstantinova, N.A. & Vasiljev, A.N. (1994) On the hepatic flora of Sayan Mountains (South Siberia). Arctoa 3: 123–132. https://doi.org/10.15298/arctoa.03.07

  164. Konstantinova, N.A. & Vilnet, A.A. (2009) New taxa and new combinations in Jungermanniales (Hepaticae). Arctoa 18: 65–67. https://doi.org/10.15298/arctoa.18.02

  165. Konstantinova, N.A., Ignatov, M.S. & Perkovsky, E.E. (2012) Hepatics from Rovno amber (Ukraine). Arctoa 21: 265‒271. https://doi.org/10.15298/arctoa.21.25

  166. Kosmowska-Ceranowicz, B. (2001) The amber treasure trove. Museum of the Earth Documentary Studies 18: 1–97.

  167. Khotimperwati, L., Kasiamdari, R.S., Santosa, S. & Daryono, B.S. (2018) Bazzania Gray (Lepidoziaceae, Marchantiophyta) in Central Java, Indonesia. Biodiversitas 19: 875–887. https://doi.org/10.13057/biodiv/d190316

  168. Krassilov, V.A. (1970) Leafy hepatics from the Jurassic of the Bureja basin. Paleontologicheskij Zhurnal 4 (3): 131–142. [in Russian]

  169. Krassilov, V.A. (1973) Mesozoic bryophytes from the Bureja basin, Far East of the USSR. Palaeontographica B 143: 95–105.

  170. Krassilov, V.A. & Schuster, R.M. (1984) Paleozoic and Mesozoic fossils. In: Schuster, R.M. (Ed.) New Manual of Bryology. The Hattori Botanical Laboratory, Nichinan, pp. 1172‒1193.

  171. Kubilius, R.A., Bölz, A., Feldberg, K., Hedenäs, L., Schäfer-Verwimp, A., Schmidt, A.R. & Heinrichs, J. (2017) The moss Helicophyllum torquatum (Bryopsida, Helicophyllaceae) has survived since at least the Miocene. Botanical Journal of the Linnean Society 185: 56‒64. https://doi.org/10.1093/botlinnean/box041

  172. Laenen, B., Shaw, B., Schneider, H., Goffinet, B., Paradis, E., Désamoré, A., Heinrichs, J., Villarreal, J.C., Gradstein, S.R., McDaniel, S.F., Long, D.G., Forrest, L.L., Hollingsworth, M.L., Crandall-Stotler, B., Davis, E.C., Engel, J., von Konrat, M., Cooper, E.D., Patiño, J., Cox, C.J., Vanderpoorten, A. & Shaw, A.J. (2014) Extant diversity of bryophytes emerged from successive post-Mesozoic diversification bursts. Nature Communications 5: 6134. https://doi.org/10.1038/ncomms6134

  173. Lee, G.E. (2013) A systematic revision of the genus Lejeunea Lib. (Marchantiophyta: Lejeuneaceae) in Malaysia. Cryptogamie, Bryologie 34: 381–484. https://doi.org/10.7872/cryb.v34.iss4.2013.381

  174. Lee, G.E., Bechteler, J., Schäfer-Verwimp, A. & Heinrichs, J. (2015a) Microlejeunea miocenica sp. nov. (Porellales, Jungermanniopsida) in Dominican amber, the first fossil of a subcosmopolitan genus of leafy liverworts. Review of Palaeobotany and Palynology 222: 16–21. https://doi.org/10.1016/j.revpalbo.2015.07.002

  175. Lee, G.E., Schäfer-Verwimp, A., Schmidt, A.R. & Heinrichs, J. (2015b) Transfer of the Miocene Lejeunea palaeomexicana Grolle to Ceratolejeunea. Cryptogamie, Bryologie 36: 335–341. https://doi.org/10.7872/cryb/v36.iss4.2015.335

  176. Lee, G.E., Kolberg, L., Bechteler, J., Schäfer-Verwimp, A., Renner, M.A.M., Schmidt, A.R. & Heinrichs, J. (2017) The leafy liverwort genus Lejeunea (Porellales, Jungermanniopsida) in Miocene Dominican amber. Review of Palaeobotany and Palynology 238: 144–150. https://doi.org/10.1016/j.revpalbo.2016.11.013

  177. Lee, G.E., Condamine, F.L., Bechteler, J., Pérez-Escobar, O.A., Scheben, A., Schäfer-Verwimp, A., Pócs, T. & Heinrichs, J. (2020) An ancient tropical origin, dispersals via land bridges and Miocene diversification explain the subcosmopolitan disjunctions of the liverwort genus Lejeunea. Scientific Reports 10: 14123. https://doi.org/10.1038/s41598-020-71039-1

  178. Lehmann, J.G.C. (1832) Novarum et minus cognitarum stirpium pugillus quartus. Meissner, Hamburg, 64 pp. https://doi.org/10.5962/bhl.title.45011

  179. Lehmann, J.G.C. (1834) Novarum et minus cognitarum stirpium pugillus sextus. Meissner, Hamburg, 72 pp. https://doi.org/10.5962/bhl.title.45011

  180. Lehmann, J.G.C. (1844) Novarum et minus cognitarum stirpium pugillus octavus. Meissner, Hamburg, 56 pp. https://doi.org/10.5962/bhl.title.45011

  181. Li, Y., Wang, Y.-D., Schneider, H. & Wu, P.-C. (2020) Frullania partita sp. nov. (Frullaniaceae, Porellales), a new leafy liverwort from the mid-Cretaceous of Myanmar. Cretaceous Research 108: 104341. https://doi.org/10.1016/j.cretres.2019.104341

  182. Li, Y., Li, L.-Q., Feldberg, K., Wu, P.-C., Schneider, H., Schmidt, A.R. & Wang, Y.-D. (2021) Re-appraisal of two fossil Frullaniaceae species (Marchantiophyta, Porellales) from the mid-Cretaceous Burmese amber. Cretaceous Research 124: 104803. https://doi.org/10.1016/j.cretres.2021.104803

  183. Libert, M.-A. (1820) Sur un genre nouveau d’hépatiques, Lejeunia. Annales générales des sciences physiques 6: 372–374.

  184. Lima, E., Ilkiu-Borges, A.L. & Gradstein, S.R. (2020) A new species of Frullania subg. Frullania (Marchantiophyta) from the Brazilian Amazon. Phytotaxa 456 (1): 119–124. https://doi.org/10.11646/phytotaxa.456.1.10

  185. Lindberg, S.O. (1872) Contributio ad floram cryptogamam Asiae boreali-orientalis. Acta Societatis Scientiarum Fennicae 10: 221–280.

  186. Lindenberg, J.B.W. (1829) Synopsis hepaticarum europaearum. Eduard Weberum, Bonnae, 133 pp.

  187. Lindenberg, J.B.W. (1840) Species hepaticarum, fasc. 2–4. Henry & Cohen, Bonn, pp. 37‒120.

  188. Linnaeus, C. (1753) Species plantarum, ed. 1. Laurentii Salvii, Holmiae [Stockholm], 1200 pp.

  189. Loeske, L. (1905) Bryologisches vom Harze und aus anderen Gebieten. Verhandlungen des Botanischen Vereins der Provinz Brandenburg 47: 317‒344.

  190. Loeske, L. (1908) Bryologische Beobachtungen aus den Algäuer Alpen von Loeske und Osterwald. Verhandlungen des Botanischen Vereins der Provinz Brandenburg 49: 30‒65.

  191. Loeske, L. (1909) Zur Moosflora der Zillertaler Alpen. Hedwigia 49: 1–53.

  192. Lóriga, J., Schmidt, A.R., Moran, R.C., Feldberg, K., Schneider, H. & Heinrichs, J. (2014) The first fossil of a bolbitidoid fern belongs to the early divergent lineages of Elaphoglossum (Dryopteridaceae). American Journal of Botany 101: 1466‒1475. https://doi.org/10.3732/ajb.1400262

  193. Magallón S., Hilu, K.W. & Quandt, D. (2013) Land plant evolutionary timeline: Gene effects are secondary to fossil constraints in relaxed clock estimation of age and substitution rates. American Journal of Botany 100: 556–573. https://doi.org/10.3732/ajb.1200416

  194. Mägdefrau, K. (1957) Flechten und Moose im baltischen Bernstein. Berichte der Deutschen Botanischen Gesellschaft 70: 433–435.

  195. Mamontov, Y.S., Heinrichs, J., Schäfer-Verwimp, A., Ignatov, M.S. & Perkovsky, E.E. (2013) Hepatics from Rovno amber (Ukraine), 2. Acrolejeunea ucrainica sp. nov. Arctoa 22: 93–96. https://doi.org/10.15298/arctoa.22.13

  196. Mamontov, Y.S., Heinrichs, J., Schäfer-Verwimp, A., Ignatov, M.S. & Perkovsky, E.E. (2015a) Hepatics from Rovno amber (Ukraine), 4. Frullania riclefgrollei, sp. nov. Review of Palaeobotany and Palynology 223: 31–36. https://doi.org/10.1016/j.revpalbo.2015.08.007

  197. Mamontov, Y.S., Heinrichs, J., Váňa, J., Ignatov, M.S. & Perkovsky, E.E. (2015b) Hepatics from Rovno amber (Ukraine), 3. Anastrophyllum rovnoi sp. nov. Arctoa 24: 43–46. https://doi.org/10.15298/arctoa.24.08

  198. Mamontov, Y.S., Heinrichs, J., Váňa, J., Ignatov, M.S. & Perkovsky, E.E. (2015c) Hepatics from Rovno amber (Ukraine), 5. Cephaloziella nadezhdae sp. nov. Arctoa 24: 289–293. https://doi.org/10.15298/arctoa.24.25

  199. Mamontov, Y.S., Hentschel, J., Konstantinova, N.A., Perkovsky, E.E. & Ignatov, M.S. (2017) Hepatics from Rovno amber (Ukraine), 6. Frullania rovnoi, sp. nov. Journal of Bryology 39: 336–341. https://doi.org/10.1080/03736687.2017.1343220

  200. Mamontov, Y.S., Ignatov, M.S. & Perkovsky, E.E. (2018a) Hepatics from Rovno amber (Ukraine), 7. Frullania zerovii, sp. nov. Nova Hedwigia 106: 103–113. https://doi.org/10.1127/nova_hedwigia/2017/0446

  201. Mamontov, Y.S., Vilnet, A.A. & Potemkin, A.D. (2018b) Scapania marsupelloides sp. nov. (Scapaniaceae, Marchantiophyta), a remarkable new species near the base of Scapania phylogeny. Phytotaxa 385 (2): 55–66. https://doi.org/10.11646/phytotaxa.385.2.1

  202. Mamontov, Y.S., Ignatov, M.S. & Perkovsky, E.E. (2019) Liverworts from Rovno amber (Ukraine). 8. Frullania ekaterinae sp. nov. and F. schmalhausenii sp. nov. Paleontological Journal 53: 1095–1103. https://doi.org/10.1134/S0031030119100113

  203. Mamontov, Y.S., Atwood, J.J., Perkovsky, E.E. & Ignatov, M.S. (2020a) Hepatics from Rovno amber (Ukraine): Frullania pycnoclada and a new species, F. vanae. The Bryologist 123: 421–430. https://doi.org/10.1639/0007-2745-123.3.421

  204. Mamontov, Y.S., Vilnet, A.A., Atwood, J.J. & Konstantinova, N.A. (2020b) Molecular phylogenetic study of Frullania subsect. Inflatae (Frullaniaceae, Marchantiophyta) in the Holarctic with description of a new subgenus and three new species. Nova Hedwigia Beiheft 150: 201–242. https://doi.org/10.1127/nova-suppl/2020/201

  205. Marshall, C.R. (2019) Using the fossil record to evaluate timetree timescales. Frontiers in Genetics 10: 1049. https://doi.org/10.3389/fgene.2019.01049

  206. Massalongo, C. & Carestia, A. (1880) Epatiche delle Alpi Pennine. Nuovo Giornale Botanico Italiano 12: 306–366. Tav. VIII–XI.

  207. Meagher, D.A. (2019) A synopsis of the genus Bazzania (Marchantiophyta: Lepidoziaceae) in Australia. Australian Systematic Botany 32: 310–362. https://doi.org/10.1071/SB18025

  208. Mitten, W. (1860a) Hepaticae Indiae Orientalis. Journal of the Proceedings of the Linnean Society. Botany 5: 89–128. https://doi.org/10.1111/j.1095-8312.1860.tb01045.x

  209. Mitten, W. (1860b) On some new species of musci and hepaticae in the herbarium of sir W. J. Hooker, collected in tropical Africa, chiefly by the late Dr. Vogel and Mr. Barger. Transactions of the Linnean Society of London 23: 51–58. https://doi.org/10.1111/j.1096-3642.1860.tb00117.x

  210. Mitten, W. (1864a) On some species of Musci and Hepaticae, additional to the floras of Japan and the coast of China. Botanical Journal of the Linnean Society 8: 148–158. https://doi.org/10.1111/j.1095-8312.1864.tb01081.x

  211. Mitten, W. (1864b) The “Bryologia” of the survey of the 48th parallel of latitude. Botanical Journal of the Linnean Society 8: 12–55. https://doi.org/10.1111/j.1095-8312.1864.tb01071.x

  212. Mitten, W. (1871) Jungermanniae and Marchantiae. In: Seemann, B. (Ed.) Flora vitiensis, part 10. Reeve, London, pp. 404–419. https://doi.org/10.5962/bhl.title.455

  213. Montagne, J.F.C. (1840) Seconde centurie de plantes cellulaires exotiques nouvelles. Décades VI, VII et VIII. Annales des Sciences Naturelles; Botanique (sér. 2) 14: 321–350.

  214. Montagne, J.F.C. (1842) Botanique. Plantes cellulaires. In: de la Sagra, R.D.J. (Ed.) Histoire Physique, Politique et Naturelle de l’Ile de Cuba. Arthus Bertrand, Paris, pp. 427–492. https://doi.org/10.5962/bhl.title.51128

  215. Morris, J.L., Puttick, M.N., Clark, J.W., Edwards, D., Kenrick, P., Pressel, S., Wellman, C.H., Yang, Z., Schneider, H. & Donoghue, P.C.J. (2017) The timescale of early land plant evolution. Proceedings of the National Academy of Sciences of the United States of America 115: E2274–E2283. https://doi.org/10.1073/pnas.1719588115

  216. Müller, K. (1904) Über die in Baden in den Jahren 1902 und 1903 gesammelten Lebermoose. Beihefte zum Botanischen Centralblatt 17: 211–233.

  217. Müller, K. (1905) Monographie der Lebermoosgattung Scapania Dum. Nova Acta Academiae Caesareae Leopoldino-Carolinae Germanicae Naturae Curiosorum 83: 1–312.

  218. Müller, K. (1912) Die Lebermoose (Dr. L. Rabenhorst‘s Kryptogamen-Flora von Deutschland, Oesterreich und der Schweiz, 2 Aufl., 6 Band), 2 Abth., 16 Lieferung. Eduard Kummer, Leipzig, pp. 81–144. https://doi.org/10.5962/bhl.title.1356

  219. Nees, C.G. (1830) Enumeratio plantarum cryptogamicarum Javae et insularum adiacentium. Grass, Barth & Co, Breslau, 86 pp.

  220. Nees, C.G. (1833a) Hepaticae Hedw. In: Martius, C.F.P. (ed.) Flora brasiliensis. Sumptibus J. G. Cottae, Stuttgart, pp. 294–390. https://doi.org/10.5962/bhl.title.454

  221. Nees, C.G. (1833b) Naturgeschichte der Europäischen Lebermoose, vol. 1. August Rücker, Berlin, 347 pp.

  222. Oostendorp, C. (1987) The bryophytes of the Paleozoic and Mesozoic. Bryophytorum Bibliotheca 34: 5–112. Plates I–XLIX.

  223. O’Reilly, J.E. & Donoghue, P.C.J. (2020) The effect of fossil sampling on the estimation of divergence times with the fossilized birth–death process. Systematic Biology 69: 124–138. https://doi.org/10.1093/sysbio/syz037

  224. Parham, J.F., Donoghue, P.C.J., Bell, C.J., Calwey, T.D., Head, J.J., Holroyd, P.A., Inoue, J.G., Irmis, R.B., Joyce, W.G., Ksepka, D.T., Patané, J.S.L., Smith, N.D., Tarver, J.E., van Tuinen, M., Yang, Z., Angielczyk, K.D., Greenwood, J.M., Hipsley, C.A., Jacobs, L., Makovicky, P.J., Müller, J., Smith, K.T., Theodor, J.M., Warnock, R.C.M. & Benton, M.J. (2012) Best practices for justifying fossil calibrations. Systematic Biology 61: 346–359. https://doi.org/10.1093/sysbio/syr107

  225. Patiño, J., Wang, J., Renner, M.A.M., Gradstein, S.R., Laenen, B., Devos, N., Shaw, A.J. & Vanderpoorten, A. (2017) Range size heritability and diversification patterns in the liverwort genus Radula. Molecular Phylogenetics and Evolution 106: 73–85. https://doi.org/10.1016/j.ympev.2016.09.020

  226. Paton, J.A. (1999) The liverwort flora of the British Isles. Harley Books, Colchester, 626 pp.

  227. Patzak, S.D.F., Renner, M.A.M., Schäfer-Verwimp, A., Feldberg, K., Heslewood, M.M., Peralta, D.F., de Souza, A.M., Schneider, H. & Heinrichs, J. (2016) A phylogeny of Lophocoleaceae-Plagiochilaceae-Brevianthaceae and a revised classification of Plagiochilaceae. Organisms Diversity and Evolution 16: 481–495. https://doi.org/10.1007/s13127-015-0258-y

  228. Pearson, W.H. (1894) Frullania microphylla. Journal of Botany, British and Foreign 32: 328–330.

  229. Penney, D. (2010) Dominican amber. In: Penney, D. (Ed.) Biodiversity of fossils in amber from the major world deposits. Siri Scientific Press, Manchester, pp. 22–41.

  230. Perkovsky, E.E., Zosimovich, V.Y. & Vlaskin, A.P. (2010) Rovno amber. In: Penney, D. (Ed.) Biodiversity of fossils in amber from the major world deposits. Siri Scientific Press, Manchester, pp. 116–136.

  231. Persson, H. (1954) On Neohodgsonia H. Perss. the new hepatic genus from New Zealand and Tristan da Cunha. Botaniska Notiser 107: 39–44.

  232. Pett, W. & Heath, T.A. (2020) Inferring the timescale of phylogenetic trees from fossil data. In: Scornavacca, C., Delsuc, F. & Galtier, N. (eds.) Phylogenetics in the genomic era. No commercial publisher, authors open access book, pp. 5.1:1–5.1:18.

  233. Pócs, T., Müller, F. & Shevock, J.R. (2015) Additions to the liverwort and hornwort flora of São Tomé and Príncipe II, with Neurolejeunea, a genus new to Africa. Herzogia 28: 50–69. https://doi.org/10.13158/heia.28.1.2015.50

  234. Potemkin, A.D. & Müller, F. (2020) The genus Scapania (Scapaniaceae, Marchantiophyta) in Myanmar. Journal of Bryology 42: 386–389. https://doi.org/10.1080/03736687.2020.1793079

  235. Potemkin, A.D., Piippo, S. & Koponen, T.J. (2004) Bryophyte flora of Hunan Province, China. 4. Diplophyllaceae and Scapaniaceae (Hepaticae). Annales Botanici Fennici 41: 415–427.

  236. Poulsen, C. (1974) Further contributions to the knowledge of the Palaeozoic of Slagelse no. 1, Western Sealand. II. Permian roots and fossils. Danmarks Geologiske Undersøgelse II 101: 28–32.

  237. Rabenhorst, G.L. (1862) Hepaticae Europaeae. Die Lebermoose Europa’s unter Mitwirkung mehrerer namhafter Botaniker, Decades 21-22. Dresden, tab. 201–220.

  238. Raddi, G. (1818) Jungermanniografia etrusca. Modena, 45 pp.

  239. Ramaiya, M., Johnson, M.G., Shaw, B., Heinrichs, J., Hentschel, J., von Konrat, M., Davison, P.G. & Shaw, A.J. (2010) Morphologically cryptic biological species within the liverwort Frullania asagrayana. American Journal of Botany 97: 1707–1718. https://doi.org/10.3732/ajb.1000171

  240. Reiner-Drehwald, M.E. & Goda, A. (2000) Revision of the genus Crossotolejeunea (Lejeuneaceae, Hepaticae). Journal of the Hattori Botanical Laboratory 89: 1–54.

  241. Reiner-Drehwald, M.E., Schmidt, A.R. & Heinrichs, J. (2012) The genus Lejeunea in Miocene amber from the Dominican Republic. Cryptogamie, Bryologie 33: 33–38. https://doi.org/10.7872/cryb.v33.iss1.2012.033

  242. Reinwardt, C.G.C., Blume, C.L. & Nees, C.G. (1824) Hepaticae Iavanicae, editae coniunctis studiis et opera. Nova Acta Physico-Medica Academiae Caesareae Leopoldino-Carolinae Naturae Curiosorum Exhibentia 12: 181–238.

  243. Renner, M.A.M. (2014) Radula subg. Radula in Australasia and the Pacific (Jungermanniopsida). Telopea 17: 107–167. https://doi.org/10.7751/telopea20147553

  244. Renner, M.A.M. (2015) Lobule shape evolution in Radula (Jungermanniopsida): one rate fits all? Botanical Journal of the Linnean Society 178: 222–242. https://doi.org/10.1111/boj.12279

  245. Renner, M.A.M. (2018) A revision of Australian Plagiochila (Lophocoleinae: Jungermanniopsida). Telopea 21: 187–380. https://doi.org/10.7751/telopea12959

  246. Renner, M.A.M. (2020) Opportunities and challenges presented by cryptic bryophyte species. Telopea 23: 41–60. https://doi.org/10.7751/telopea14083

  247. Renner, M.A.M., Devos, N., Brown, E.A. & von Konrat, M.J. (2013a) Three modes of heterochrony explain lobule diversity in Radula subgenus Cladoradula (Porellales: Jungermanniopsida), a small lineage of early land plants today. Botanical Journal of the Linnean Society 173: 153–175. https://doi.org/10.1111/boj.12087

  248. Renner, M.A.M., Devos, N., Patiño, J., Brown, E.A., Orme, A., Elgey, M., Wilson, T.C., Gray, L.J. & von Konrat, M.J. (2013b) Integrative taxonomy resolves the cryptic and pseudo-cryptic Radula buccinifera complex (Porellales, Jungermanniopsida), including two reinstated and five new species. PhytoKeys 27: 1–113. https://doi.org/10.3897/phytokeys.27.5523

  249. Renner, M.A.M., Brown, E.A. & Wardle, G.M. (2013c) Averaging v. outlier removal. Decrypting variance among cryptic Lejeunea species (Lejeuneaceae: Jungermanniopsida) using geometric morphometrics. Australian Systematic Botany 26: 13–30. https://doi.org/10.1071/SB12016

  250. Renner, M.A.M, Hesslewood, M.M., Patzak, S.D.F., Schäfer-Verwimp, A. & Heinrichs, J. (2017a) By how much do we underestimate species diversity of liverworts using morphological evidence? An example from Australasian Plagiochila (Plagiochilaceae: Jungermanniopsida). Molecular Phylogenetics and Evolution 107: 576–593. https://doi.org/10.1016/j.ympev.2016.12.018

  251. Renner, M.A.M., Patzak, S.D.F., Heslewood, M.M., Schäfer-Verwimp, A. & Heinrichs, J. (2017b) Third time lucky? Another substantially revised sectional classification for Australasian Plagiochila (Plagiochilaceae: Jungermanniopsida). Australian Systematic Botany 30: 70–104. https://doi.org/10.1071/SB16038

  252. Renzaglia, K.S., Crandall-Stotler, B., Pressel, S., Duckett, J.G., Schuette, S. & Strother, P.K. (2015) Permanent spore dyads are not ‘a thing of the past’: on their occurrence in the liverwort Haplomitrium (Haplomitriopsida). Botanical Journal of the Linnean Society 179: 658–669. https://doi.org/10.1111/boj.12343

  253. Rikkinen, J. & Poinar, G.O. Jr. (2008) A new species of Phyllopsora (Lecanorales, lichen-forming Ascomycota) from Dominican amber, with remarks on the fossil history of lichens. Journal of Experimental Botany 59: 1007–1011. https://doi.org/10.1093/jxb/ern004

  254. Ross, A., Mellish, C., York, P. & Crighton, B. (2010) Burmese amber. In: Penney, D. (Ed.) Biodiversity of fossils in amber from the major world deposits. Siri Scientific Press, Manchester, pp. 208–235.

  255. Rust, J., Singh, H., Rana, R.S., McCann, T., Singh, L., Anderson, K., Sarkar, N., Nascimbene, P.C., Stebner, F., Thomas, J.C., Solórzano Kraemer, M., Williams, C.J., Engel, M.S., Sahni, A. & Grimaldi, D. (2010) Biogeographic and evolutionary implications of a diverse paleobiota in amber from the early Eocene of India. Proceedings of the National Academy of Sciences of the United States of America 107: 18360–18365. https://doi.org/10.1073/pnas.1007407107

  256. Sadowski, E.-M., Schmidt, A.R., Seyfullah, L.J. & Kunzmann, L. (2017) Conifers of the ‘Baltic amber forest’ and their palaeoecological significance. Stapfia 106: 1–73.

  257. Scheben, A., Bechteler, J., Lee, G.E., Pócs, T., Schäfer-Verwimp, A. & Heinrichs, J. (2016) Multiple transoceanic dispersals and geographical structure in the pantropical leafy liverwort Ceratolejeunea (Lejeuneaceae, Porellales). Journal of Biogeography 43: 1739–1749. https://doi.org/10.1111/jbi.12779

  258. Schiffner, V. (1893) Hepaticae. In: Engler, A. & Prantl, K. (Eds.) Die Natürlichen Pflanzenfamilien, Teil I, Abt. 3. Engelmann, Leipzig, pp. 1–141. https://doi.org/10.5962/bhl.title.4635

  259. Schiffner, V. (1898) Conspectus hepaticarum archipelagi indici. Staatsdruckerei, Batavia, 382 pp.

  260. Schiffner, V. (1900) Die Hepaticae der Flora von Buitenzorg. I. Band. E. J. Brill, Leiden, 220 pp.

  261. Schljakov, R.N. (1976) Combinationes et taxa anthocerotarum et hepaticarum nova. Novosti Sistematiki Nizših Rastenij 13: 225–229.

  262. Schljakov, R.N. (1979) Additamenta nova ad floram hepaticarum regionum septentrionalium URSS. Novosti Sistematiki Nizših Rastenij 16: 201–208.

  263. Schneider, H., Schmidt, A.R., Nascimbene, P.C. & Heinrichs, J. (2015) A new Dominican amber fossil of the derived fern genus Pleopeltis confirms generic stasis in the epiphytic fern diversity of the West Indies. Organisms Diversity and Evolution 15: 277–283.  https://doi.org/10.1007/s13127-015-0200-3

  264. Schneider, H., Schmidt, A.R. & Heinrichs, J. (2016) Burmese amber fossils bridge the gap in the Cretaceous record of polypod ferns. Perspectives in Plant Ecology, Evolution and Systematics 18: 70–78. https://doi.org/10.1016/j.ppees.2016.01.003

  265. Schrader, H.A. (1797) Systematische Sammlung cryptogamischer Gewächse, Zweyte Lieferung. J.C. Dietrich, Göttingen, 16 pp.

  266. Schuster, R.M. (1956) North American Lejeuneaceae. V. Schizostipae: Ceratolejeunea. Journal of the Elisha Mitchell Scientific Society 72: 292–316.

  267. Schuster, R.M. (1963) An annotated synopsis of the genera and subgenera of Lejeuneaceae. I. Beihefte zur Nova Hedwigia 9: 1–203.

  268. Schuster, R.M. (1968) Studies on the hepaticae, XXIX-XLIV. A miscellany of new taxa and new range extensions. Nova Hedwigia 15: 437–529.

  269. Schuster, R.M. (1969) The hepaticae and anthocerotae of North America. II. Columbia University Press, New York, 1062 pp.

  270. Schuster, R.M. (1970) Studies on antipodal hepaticae, III. Jubulopsis Schuster, Neohattoria Kamimura and Amphijubula Schuster. Journal of the Hattori Botanical Laboratory 33: 266–304.

  271. Schuster, R.M. (1971) The ecology and distribution of hepaticae in a mahogany hammock in tropical Florida. Castanea 36: 90–111.

  272. Schuster, R.M. (1978) Studies on Venezuelan hepaticae. I. Phytologia 39: 239–251. https://doi.org/10.5962/bhl.part.7614

  273. Schuster, R.M. (1980) The hepaticae and anthocerotae of North America. IV. Columbia University Press, New York, 1334 pp.

  274. Schuster, R.M. (1981) Paleoecology, origin, distribution through time, and evolution of hepaticae and anthocerotae. In: Niklas, K.J. (ed.) Paleobotany, paleoecology, and evolution, vol. 2. Praeger, New York, pp. 129–191.

  275. Schuster, R.M. (1985) Studies in Porellineae: New taxa of Jubulaceae. Phytologia 57: 369–373.

  276. Schuster, R.M. (1992) The hepaticae and anthocerotae of North America. V. Columbia University Press, New York, 854 pp.

  277. Schuster, R.M. (2000) Austral hepaticae. Part I. Nova Hedwigia Beiheft 118: 1–524.

  278. Schuster, R.M. (2002) Austral hepaticae. Part II. Nova Hedwigia Beiheft 119: 1–606.

  279. Schuster, R.M. & Janssens, J.A. (1989) On Diettertia, an isolated Mesozoic member of the Jungermanniales. Review of Palaeobotany and Palynology 57: 277–287. https://doi.org/10.1016/0034-6667(89)90025-0

  280. Scott, E.B. (1980) Jungermannites noterocladioides n. sp. (Hepaticae) from the Potomac Group (Lower Cretaceous) of Maryland, USA. Journal of Paleontology 54: 1119–1121.

  281. Serrano-Sánchez, M. de L., Hegna, T.A., Schaaf, P., Pérez, L., Centeno-García, E. & Vega, F.J. (2015) The aquatic and semiaquatic biota in Miocene amber from the Campo LA Granja mine (Chiapas, Mexico): Paleoenvironmental implications. Journal of South American Earth Sciences 62: 243–256. https://doi.org/10.1016/j.jsames.2015.06.007

  282. Shaw, A.J. (2001) Biogeographic patterns and cryptic speciation in bryophytes. Journal of Biogeography 28: 253–261. https://doi.org/10.1046/j.1365-2699.2001.00530.x

  283. Shaw, B., Crandall-Stotler, B., Váňa, J., Stotler, R.E., von Konrat, M., Engel, J.J., Davis, E.C., Long, D.G., Sova, P. & Shaw, A.J. (2015) Phylogenetic relationships and morphological evolution in a major clade of leafy liverworts (phylum Marchantiophyta, order Jungermanniales): suborder Jungermanniineae. Systematic Botany 40: 27–45. https://doi.org/10.1600/036364415X686314

  284. Shi, G., Grimaldi, D.A., Harlow, G.E., Wang, J., Wang, J., Yang, M., Lei, W., Li, Q. & Li, X. (2012) Age constraint on Burmese amber based on U–Pb dating of zircons. Cretaceous Research 37: 155–163. https://doi.org/10.1016/j.cretres.2012.03.014

  285. Shi, X.-Q., Gradstein, S.R. & Zhu R.-L. (2015) Phylogeny and taxonomy of Archilejeunea (Marchantiophyta: Lejeuneaceae) based on molecular markers and morphology. Taxon 64: 881–892. https://doi.org/10.12705/645.1

  286. Silva, S.E., Silva, D.N., Almeida, T., Garcia, C.A., Paulo, O.S. & Sim-Sim, M. (2017) Age estimates of Frullania (Frullaniaceae, Porellales) main lineages: another example of rapid and recent diversification in liverwort evolution. Systematics and Biodiversity 15: 156–165. https://doi.org/10.1080/14772000.2016.1217096

  287. Söderström, L. & Séneca, A. (2006) World distribution patterns in the Lophoziaceae/Scapaniaceae complex (Hepaticae, Bryophyta). Journal of the Hattori Botanical Laboratory 100: 431–441.

  288. Söderström, L., Weibull, H. & Damsholt, K. (2000) A new species of Lophozia (subgen. Protolophozia) from Fennoscandia. Lindbergia 25: 3–7.

  289. Söderström, L., De Roo, R. & Hedderson, T. (2010) Taxonomic novelties resulting from recent reclassification of the Lophoziaceae/Scapaniaceae clade. Phytotaxa 3: 47–53. https://doi.org/10.11646/phytotaxa.3.1.7

  290. Söderström, L., Hagborg, A., von Konrat, M., Bartholomew-Began, S., Bell, D., Briscoe, L., Brown, E., Cargill, D.C., Costa, D.P., Crandall-Stotler, B.J., Cooper, E.D., Dauphin, G., Engel, J.J., Feldberg, K., Glenny, D., Gradstein, S.R., He, X., Heinrichs, J., Hentschel, J., Ilkiu-Borges, A.L., Katagiri, T., Konstantinova, N.A., Larraín, J., Long, D.G., Nebel, M., Pócs, T., Puche, F., Reiner-Drehwald, E., Renner, M.A.M., Sass-Gyarmati, A., Schäfer-Verwimp, A., Segarra Moragues, J.G., Stotler, R.E., Sukkharak, P., Thiers, B.M., Uribe, J., Váňa, J., Villarreal, J.C., Wigginton, M., Zhang, L. & Zhu, R.-L. (2016) World checklist of hornworts and liverworts. PhytoKeys 59: 1–828. https://doi.org/10.3897/phytokeys.59.6261

  291. Solórzano Kraemer, M.M. (2010) Mexican amber. In: Penney, D. (Ed.) Biodiversity of fossils in amber from the major world deposits. Siri Scientific Press, Manchester, pp. 42–56.

  292. Spruce, R. (1884) Hepaticae amazonicae et andinae. I. Transactions and Proceedings of the Botanical Society of Edinburgh 15: 1–308. https://doi.org/10.5962/bhl.title.115637

  293. Spruce, R. (1885) Hepaticae amazonicae et andinae. II. Transactions and Proceedings of the Botanical Society of Edinburgh 15: 309–588. https://doi.org/10.5962/bhl.title.115637

  294. Steere, W.C. (1946) Cenozoic and Mesozoic bryophytes of North America. The American Midland Naturalist 36: 298–324. https://doi.org/10.2307/2421507

  295. Stephani, F. (1886a) Hepaticae africanae. Botanische Jahrbücher für Systematik, Pflanzengeschichte und Pflanzengeographie 8: 79–95.

  296. Stephani, F. (1886b) Hepaticae von der Halbinsel Alaska, gesammelt 1881/82 von den Doctoren Arthur und Aurel Krause. Botanische Jahrbücher für Systematik, Pflanzengeschichte und Pflanzengeographie 8: 96–99.

  297. Stephani, F. (1888a) Hepaticae africanae. Hedwigia 27: 59–63.

  298. Stephani, F. (1888b) Hepaticae africanae. Hedwigia 27: 106–113.

  299. Stephani, F. (1890) Hepaticae africanae novae in insulis Bourbon, Maurice et Madagascar lectae. Botanical Gazette 15: 281–292. https://doi.org/10.1086/326585

  300. Stephani, F. (1891) Hepaticae africanae. Hedwigia 30: 201–217.

  301. Stephani, F. (1892) The North American Lejeuneae. Botanical Gazette 17: 170–173. https://doi.org/10.1086/326806

  302. Stephani, F. (1893) Hepaticarum species novae. Pars II. Hedwigia 32: 137–147.

  303. Stephani, F. (1895) Hepaticae. In: Engler, A. (Ed.) Die Pflanzenwelt Ost-Afrikas und der Nachbargebiete. Theil C. Verzeichniss der bis jetzt aus Ost-Afrika bekannt gewordenen Pflanzen. Dietrich Reimer Verlag, Berlin, pp. 62–66. https://doi.org/10.5962/bhl.title.587

  304. Stephani, F. (1896a) Hepaticae. In: Reinecke, F. (Ed.) Die Flora der Samoa Inseln. Botanische Jahrbücher für Systematik, Pflanzengeschichte und Pflanzengeographie 23: 237–368.

  305. Stephani, F. (1896b) Hepaticarum species novae IX. Hedwigia 35: 73–140.

  306. Stephani, F. (1902) Species hepaticarum 2. Bulletin de l’Herbier Boissier (sér. 2) 2: 35–48. https://doi.org/10.5962/bhl.title.95494

  307. Stephani, F. (1904) Hepaticarum species novae X. Hedwigia 44: 14–15.

  308. Stephani, F. (1908) Species hepaticarum 3. Bulletin de l’Herbier Boissier (sér. 2) 8: 483–514. https://doi.org/10.5962/bhl.title.95494

  309. Stephani, F. (1910) Species hepaticarum 4. George & Cie, Genève & Bale, pp. 97–448. https://doi.org/10.5962/bhl.title.95494

  310. Stephani, F. (1915) Species hepaticarum 5. George & Cie, Genève & Bale, pp. 705–832. https://doi.org/10.5962/bhl.title.95494

  311. Stephani, F. (1922) Species hepaticarum 6. George & Cie, Genève & Bale, pp. 241–368. https://doi.org/10.5962/bhl.title.45014

  312. Stephani, F. (1924) Species hepaticarum 6. George & Cie, Genève & Bale, pp. 433–622. https://doi.org/10.5962/bhl.title.45014

  313. Stotler, R.E. & Crandall-Stotler, B. (2017) A synopsis of the liverwort flora of North America North of Mexico. Annals of the Missouri Botanical Garden 102: 574‒709. https://doi.org/10.3417/2016027

  314. Sukkharak, P. & Gradstein, S.R. (2014) A taxonomic revision of the genus Mastigolejeunea (Marchantiophyta: Lejeuneaceae). Nova Hedwigia 99: 279–345. https://doi.org/10.1127/0029-5035/2014/0206

  315. Sukkharak, P. & Gradstein, S.R. (2017) Phylogenetic study of Mastigolejeunea (Marchantiophyta: Lejeuneaceae) and an amended circumscription of the genus Thysananthus. Phytotaxa 326 (2): 91–107. https://doi.org/10.11646/phytotaxa.326.2.1

  316. Sun, L.-W., Gradstein, S.R., Dai, Z., Ma, W.-Z., Shi, R.-P., Wei, Q.-Q., Gao, X.-D. & Wang, J. (2018) Notes on the distribution of Acrolejeunea sandvicensis (Gottsche) Steph., a liverwort species disjunctive between East Asia and Hawaii. Phytotaxa 367 (2): 158–164. https://doi.org/10.11646/phytotaxa.367.2.5

  317. Sun, Y., He, X. & Glenny, D. (2014) Transantarctic disjunctions in Schistochilaceae (Marchantiophyta) explained by early extinction events, post-Gondwanan radiations and palaeoclimatic changes. Molecular Phylogenetics and Evolution 76: 189–201. https://doi.org/10.1016/j.ympev.2014.03.018

  318. Sundue, M. & Poinar, G. Jr. (2016) An extinct grammitid fern genus from Dominican amber, with revision of Grammitis succinea. Review of Palaeobotany and Palynology 233: 193–198. https://doi.org/10.1016/j.revpalbo.2016.04.004

  319. Swartz, O. (1788) Nova genera et species plantarum prodromus. Bibliopolio. I.G. Mülleriano, Lipsiae [Leipzig], 152 pp.

  320. Taylor, T. (1846) New hepaticae. London Journal of Botany 5: 365–417.

  321. Taylor, W.A., Strother, P.K., Vecoli, M. & Al-Hajri, S. (2017) Wall ultrastructure of the oldest embryophytic spores: Implications for early land plant evolution. Revue de Micropaléontologie 60: 281–288. https://doi.org/10.1016/j.revmic.2016.12.002

  322. Tomescu, A.M.F., Bomfleur, B., Bippus, A.C. & Savoretti, A. (2018) Why are bryophytes so rare in the fossil record? A spotlight on taphonomy and fossil preservation. In: Krings, M., Cúneo, N.R., Harper, C.J. & Rothwell, G.W. (Eds.) Transformative Paleobotany. Papers to commemorate the life and legacy of Thomas N. Taylor. Elsevier/Academic Press, New York, pp. 375–416. https://doi.org/10.1016/B978-0-12-813012-4.00016-4

  323. Townrow, J.A. (1959) Two Triassic bryophytes from South Africa. Journal of South African Botany 25: 1–22.

  324. Trevisan de Saint-Léon, V.B.A. (1877) Schema di una nuova classificazione delle Epatiche. Memorie del Reale Istituto Lombardo di Scienze e Lettere, Serie 3, Classe di Scienze Matematiche e Naturali 4: 383–451.

  325. Vainio, E. (1878) Itä-Hämeen kasvistosta [Florula tavastiae orientalis]. Meddelanden af Societas pro Fauna et Flora Fennica 3: 1–121.

  326. Váňa, J. & Long, D.G. (2009) Jungermanniaceae of the Sino-Himalayan region. Nova Hedwigia 89: 485–517. https://doi.org/10.1127/0029-5035/2009/0089-0485

  327. Váňa, J., Söderström, L., Hagborg, A. & von Konrat, M. (2013a) Notes on Early Land Plants Today. 24. What is Protolophozia? (Cephaloziellaceae, Marchantiophyta). Phytotaxa 76 (3): 50–54. https://doi.org/10.11646/phytotaxa.76.3.12

  328. Váňa, J., Söderström, L., Hagborg, A. & von Konrat, M. (2013b) Notes on Early Land Plants Today. 41. New combinations and synonyms in Cephaloziaceae (Marchantiophyta). Phytotaxa 112 (1): 7–15. https://doi.org/10.11646/phytotaxa.112.1.2

  329. Váňa, J., Schäfer-Verwimp, A., Bechteler, J., Schmidt, A.R. & Heinrichs, J. (2015a) Notoscyphus grollei sp. nov. in Bitterfeld amber rather than the extant Notoscyphus lutescens (Lehm. & Lindenb.) Mitt. Phytotaxa 222 (2): 151–154. https://doi.org/10.11646/phytotaxa.222.2.8

  330. Váňa, J., Schäfer-Verwimp, A., Bechteler, J., Schmidt, A.R. & Heinrichs, J. (2015b) Transfer of the Eocene Jungermannia berendtii Grolle to Solenostoma. Cryptogamie, Bryologie 36: 285–288. https://doi.org/10.7872/cryb/v36.iss3.2015.285

  331. Verdoorn, F. (1930) Die Frullaniaceae der Indomalesischen Inseln (De Frullaniaceis VII). Annales Bryologici, suppl. 1: 1–187.

  332. Verdoorn, F. (1934) De Frullaniaceis XV. Die Lejeuneaceae Holostipae der Indomalaya unter Berücksichtung sämtlicher aus Asien, Australien, Neuseeland und Ozeanien angeführten Arten. Annales Bryologici, suppl. 4: 40–192. https://doi.org/10.1007/978-94-015-5442-8_2

  333. Villarreal, J.C. & Renner, S.S. (2014) A review of molecular-clock calibrations and substitution rates in liverworts, mosses, and hornworts, and a timeframe for a taxonomically cleaned-up genus Nothoceros. Molecular Phylogenetics and Evolution 78: 25–35. https://doi.org/10.1016/j.ympev.2014.04.014

  334. Villarreal, J.C., Crandall-Stotler, B.J., Hart, M.L., Long, D.G. & Forrest, L.L. (2016) Divergence times and the evolution of morphological complexity in an early land plant lineage (Marchantiopsida) with a slow molecular rate. New Phytologist 209: 1734–1746. https://doi.org/10.1111/nph.13716

  335. Vilnet, A.A., Konstantinova, N.A. & Troitsky, A.V. (2008) Phylogeny and systematics of the genus Lophozia s. str. (Dumort.) Dumort. (Hepaticae) and related taxa from nuclear ITS1–2 and chloroplast trnL-F sequences. Molecular Phylogenetics and Evolution 47: 403–418. https://doi.org/10.1016/j.ympev.2007.12.013

  336. Vilnet, A.A., Konstantinova, N.A. & Troitsky, A. V. (2010) Molecular insight on phylogeny and systematics of the Lophoziaceae, Scapaniaceae, Gymnomitriaceae and Jungermanniaceae. Arctoa 19: 31–50. https://doi.org/10.15298/arctoa.19.02

  337. Vilnet, A.A., Konstantinova, N.A. & Troitsky, A.V. (2012) Molecular phylogeny and systematics of the suborder Cephaloziineae with special attention to the family Cephaloziaceae s.l. (Jungermanniales, Marchantiophyta). Arctoa 21: 113–132. https://doi.org/10.15298/arctoa.21.11

  338. von Konrat, M.J. & Braggins, J.E. (2001) A taxonomic assessment of the initial branching appendages in the liverwort genus Frullania Raddi. Nova Hedwigia 72: 283–310. https://doi.org/10.1127/nova.hedwigia/72/2001/283

  339. von Konrat, M., Braggins, J.E., Asakawa, Y. & Toyota, M. (2006) Frullania chevalieri (Jubulaceae) in New Zealand, with a reassessment of Schusterella. The Bryologist 109: 141–156. https://doi.org/10.1639/0007-2745(2006)109[141:FCJINZ]2.0.CO;2

  340. von Konrat, M., Hentschel, J., Heinrichs, J., Braggins, J.E. & Pócs, T. (2010) Forty-one degrees below and sixty years in the dark: Frullania sect. Inconditum, a new section of Australasian Frullania species including F. colliculosa, sp. nov., F. hodgsoniae, nom. and stat. nov., F. aterrima, and F. hattorii (Frullaniaceae, Marchantiophyta). Nova Hedwigia 91: 471–500. https://doi.org/10.1127/0029-5035/2010/0091-0471

  341. von Konrat, M., Hentschel, J., Heinrichs, J. & Braggins, J.E. (2011) Deep southern hemisphere connections: a revision of Frullania sect. Amphijubula. The Bryologist 114: 52–66. https://doi.org/10.1639/0007-2745-114.1.52

  342. von Konrat, M., de Lange, P., Greif, M., Strozier, L., Hentschel, J. & Heinrichs, J. (2012) Frullania knightbridgei, a new liverwort (Frullaniaceae, Marchantiophyta) species from the deep south of Aotearoa-New Zealand based on an integrated evidence-based approach. PhytoKeys 8: 13–36. https://doi.org/10.3897/phytokeys.8.2496

  343. von Konrat, M., de Lange, P., Larraín, J., Hentschel, J., Carter, B., Shaw, J. & Shaw, B. (2013) A small world: uncovering hidden diversity in Frullania—a new species from Aotearoa-New Zealand. Polish Botanical Journal 58: 437–447. https://doi.org/10.2478/pbj-2013-0056

  344. Walton, J. (1925) Carboniferous Bryophyta. I. Hepaticae. Annals of Botany 39: 563–572, Pl. XIII. https://doi.org/10.1093/oxfordjournals.aob.a089964

  345. Wang, J., Gradstein, S.R., Shi, X.-Q. & Zhu, R.-L. (2014) Phylogenetic position of Trocholejeunea and a new infrageneric classification of Acrolejeunea (Lejeuneaceae, Marchantiophyta). Bryophyte Diversity and Evolution 36: 31–44. https://doi.org/10.11646/bde.36.1.3

  346. Wang, J., Gradstein, S.R., Shi, X.-Q., Zhu, R.-L. & Do, V.T. (2015) On the occurrence of asymmetrical underleaves associated with left-right symmetry in Spruceanthus mamillilobulus (Herzog) Verd. (Lejeuneaceae), a little-known species from China and Vietnam. Journal of Bryology 37: 62–67. https://doi.org/10.1179/1743282014Y.0000000134

  347. Wang, J., Zhu, R.-L. & Gradstein, S.R. (2016) Taxonomic revision of Lejeuneaceae subfamily Ptychanthoideae (Marchantiophyta) in China. Bryophytorum Bibliotheca 65: 1–141.

  348. Warnock, R.C.M., Parham, J.F., Joyce, W.G., Lyson, T.R. & Donoghue, P.C.J. (2015) Calibration uncertainty in molecular dating analyses: there is no substitute for the prior evaluation of time priors. Proceedings of the Royal Society B 282: 20141013. https://doi.org/10.1098/rspb.2014.1013

  349. Warnock, R.C.M., Yang, Z. & Donoghue, P.C.J. (2017) Testing the molecular clock using mechanistic models of fossil preservation and molecular evolution. Proceedings of the Royal Society B 284: 20170227. https://doi.org/10.1098/rspb.2017.0227

  350. Weber, G.H. (1778) Spicilegium florae goettingensis. Sumptibus Ettingeri, Gothae [Gotha], 288 pp.

  351. Weber, F. (1815) Historiae muscorum hepaticarum prodromus. Aug. Hesse, Academiae bibliopolae, Kiel, 160 pp.

  352. Weis, G. (2001) Morphologische und anatomische Untersuchungen der Sporophyten bei den Jubulaceae Klinggr. und Lejeuneaceae Casares-Gil (Hepaticae) und deren systematische Bedeutung. Bryophytorum Bibliotheca 57: 1–302.

  353. Weitschat, W. & Wichard, W. (2002) Atlas of plants and animals in Baltic amber. Dr. Friedrich Pfeil, München, 256 pp.

  354. Wigginton, M.J. (2004) E.W. Jones’s liverwort and hornwort flora of West Africa. Meise, National Botanic Garden, Belgium, 443 pp.

  355. Wilson, R., Heinrichs, J., Hentschel, J., Gradstein, S.R. & Schneider, H. (2007) Steady diversification of derived liverworts under Tertiary climatic fluctuations. Biology Letters 3: 566–569. https://doi.org/10.1098/rsbl.2007.0287

  356. Wilson, W. (1841) Musci americani. Warrington, 180 pp.

  357. Winter, G. & Schäfer-Verwimp, A. (2020) Re-evaluation of the taxonomic status of Frullania caulisequa and Frullania obcordata (Frullaniaceae, Marchantiophyta). Frahmia 19: 1–21.

  358. Yamada, K. (1979) A revision of Asian taxa of Radula, Hepaticae. Journal of the Hattori Botanical Laboratory 45: 201–322.

  359. Yamada, K. (1984) A Radula collection made by Dr M. L. Hicks in Queensland, Australia. Cryptogamie: Bryologie-Lichénologie 5: 191–199.

  360. Yang, X.J. & Wu, X.W. (2011) Sinolejeunea yimaensis gen. et sp. nov. (Hepaticae) from the Middle Jurassic Yima Formation in Henan Province of China. Science China Earth Sciences 54: 228–232. https://doi.org/10.1007/s11430-010-4153-2

  361. Yang, Z. (2007) PAML 4: phylogenetic analysis by maximum likelihood. Molecular Biology and Evolution 24: 1586–1591. https://doi.org/10.1093/molbev/msm088

  362. Ye, W. & Zhu, R.-L. (2010) Leucolejeunea, a new synonym of Cheilolejeunea (Lejeuneaceae), with special reference to new combinations and nomenclature. Journal of Bryology 32: 279–282. https://doi.org/10.1179/037366810X12814321877507

  363. Ye, W., Gradstein, S.R., Shaw, A.J., Shaw, B., Ho, B.-C., Schäfer-Verwimp, A., Pócs, T., Heinrichs, J. & Zhu, R.-L. (2015) Phylogeny and classification of Lejeuneaceae subtribe Cheilolejeuneinae (Marchantiophyta) based on nuclear and plastid molecular markers. Cryptogamie, Bryologie 36: 313–333. https://doi.org/10.7872/cryb/v36.iss4.2015.313

  364. Yu, N.N., Gradstein, S.R. & Narengaowa (2020) Thysananthus weiweianus N.-N. Yu & Gradst. (Jungermanniopsida: Lejeuneaceae), a new fossil species in Dominican amber. Chenia 14: 58–62.

  365. Yu, T., Kelly, R., Mu, L., Ross, A., Kennedy, J., Broly, P., Xia, F., Zhang, H., Wang, B. & Dilcher, D. (2019) An ammonite trapped in Burmese amber. Proceedings of the National Academy of Sciences of the United States of America 116: 11345–11350. https://doi.org/10.1073/pnas.1821292116

  366. Zhou, L.-P., Zhang, L. & Xing, F.-W. (2012) The genus Bazzania in China and adjacent regions. 1. Bazzania dulongensis L.-P.Zhou & L.Zhang sp. nov. and Bazzania hainanensis L.-P. Zhou & L.Zhang sp. nov. Journal of Bryology 34: 22–31. https://doi.org/10.1179/1743282011Y.0000000039