|"Hepaticae" from Ernst Haeckel's Kunstformen der Natur, 1904|
Stotler & Stotl.-Crand., 1977 emend. 2000
|Classes and orders|
The Marchantiophyta (/ - /, (listen)) are a division of non-vascular land plants commonly referred to as hepatics or liverworts. Like mosses and hornworts, they have a gametophyte-dominant life cycle, in which cells of the plant carry only a single set of genetic information.
It is estimated that there are about 9000 species of liverworts. Some of the more familiar species grow as a flattened leafless thallus, but most species are leafy with a form very much like a flattened moss. Leafy species can be distinguished from the apparently similar mosses on the basis of a number of features, including their single-celled rhizoids. Leafy liverworts also differ from most (but not all) mosses in that their leaves never have a costa (present in many mosses) and may bear marginal cilia (very rare in mosses). Other differences are not universal for all mosses and liverworts, but the occurrence of leaves arranged in three ranks, the presence of deep lobes or segmented leaves, or a lack of clearly differentiated stem and leaves all point to the plant being a liverwort. Liverworts are distinguished from mosses in having unique complex oil bodies of high refractive index.
Liverworts are typically small, usually from 2–20 mm wide with individual plants less than 10 cm long, and are therefore often overlooked. However, certain species may cover large patches of ground, rocks, trees or any other reasonably firm substrate on which they occur. They are distributed globally in almost every available habitat, most often in humid locations although there are desert and Arctic species as well. Some species can be a nuisance in shady greenhouses or a weed in gardens.
Most liverworts are small, measuring from 2–20 millimetres (0.08–0.8 in) wide with individual plants less than 10 centimetres (4 in) long, so they are often overlooked. The most familiar liverworts consist of a prostrate, flattened, ribbon-like or branching structure called a thallus (plant body); these liverworts are termed thallose liverworts. However, most liverworts produce flattened stems with overlapping scales or leaves in two or more ranks, the middle rank is often conspicuously different from the outer ranks; these are called leafy liverworts or scale liverworts. (See the gallery below for examples.)
Liverworts can most reliably be distinguished from the apparently similar mosses by their single-celled rhizoids. Other differences are not universal for all mosses and all liverworts; but the lack of clearly differentiated stem and leaves in thallose species, or in leafy species the presence of deeply lobed or segmented leaves and the presence of leaves arranged in three ranks, as well as frequent dichotomous branching, all point to the plant being a liverwort. Unlike any other embryophytes, most liverworts contain unique membrane-bound oil bodies containing isoprenoids in at least some of their cells, lipid droplets in the cytoplasm of all other plants being unenclosed. The overall physical similarity of some mosses and leafy liverworts means that confirmation of the identification of some groups can be performed with certainty only with the aid of microscopy or an experienced bryologist.
Liverworts, like other bryophytes, have a gametophyte-dominant life cycle, with the sporophyte dependent on the gametophyte. The sporophyte of many liverworts are non-photosynthetic, but there are also several that are photosynthetic to various degrees. Cells in a typical liverwort plant each contain only a single set of genetic information, so the plant's cells are haploid for the majority of its life cycle. This contrasts sharply with the pattern exhibited by nearly all animals and by vascular plants. In the more familiar seed plants, the haploid generation is represented only by the tiny pollen and the ovule, while the diploid generation is the familiar tree or other plant. Another unusual feature of the liverwort life cycle is that sporophytes (i.e. the diploid body) are very short-lived, withering away not long after releasing spores. In mosses, the sporophyte is more persistent and in hornworts, the sporophyte disperses spores over an extended period.
The life of a liverwort starts from the germination of a haploid spore to produce a protonema, which is either a mass of thread-like filaments or a flattened thallus. The protonema is a transitory stage in the life of a liverwort, from which will grow the mature gametophore ("gamete-bearer") plant that produces the sex organs. The male organs are known as antheridia (singular: antheridium) and produce the sperm cells. Clusters of antheridia are enclosed by a protective layer of cells called the perigonium (plural: perigonia). As in other land plants, the female organs are known as archegonia (singular: archegonium) and are protected by the thin surrounding perichaetum (plural: perichaeta). Each archegonium has a slender hollow tube, the "neck", down which the sperm swim to reach the egg cell.
Liverwort species may be either dioicous or monoicous. In dioicous liverworts, female and male sex organs are borne on different and separate gametophyte plants. In monoicous liverworts, the two kinds of reproductive structures are borne on different branches of the same plant. In either case, the sperm must move from the antheridia where they are produced to the archegonium where the eggs are held. The sperm of liverworts is biflagellate, i.e. they have two tail-like flagellae that enable them to swim short distances, provided that at least a thin film of water is present. Their journey may be assisted by the splashing of raindrops. In 2008, Japanese researchers discovered that some liverworts are able to fire sperm-containing water up to 15 cm in the air, enabling them to fertilize female plants growing more than a metre from the nearest male.
When sperm reach the archegonia, fertilisation occurs, leading to the production of a diploid sporophyte. After fertilisation, the immature sporophyte within the archegonium develops three distinct regions: (1) a foot, which both anchors the sporophyte in place and receives nutrients from its "mother" plant, (2) a spherical or ellipsoidal capsule, inside which the spores will be produced for dispersing to new locations, and (3) a seta (stalk) which lies between the other two regions and connects them. The sporophyte lacks an apical meristem, an auxin-sensitive point of divergence with other land plants some time in the Late Silurian/Early Devonian. When the sporophyte has developed all three regions, the seta elongates, pushing its way out of the archegonium and rupturing it. While the foot remains anchored within the parent plant, the capsule is forced out by the seta and is extended away from the plant and into the air. Within the capsule, cells divide to produce both elater cells and spore-producing cells. The elaters are spring-like, and will push open the wall of the capsule to scatter themselves when the capsule bursts. The spore-producing cells will undergo meiosis to form haploid spores to disperse, upon which point the life cycle can start again.
Some liverworts are capable of asexual reproduction; in bryophytes in general "it would almost be true to say that vegetative reproduction is the rule and not the exception." For example, in Riccia, when the older parts of the forked thalli die, the younger tips become separate individuals.
Some thallose liverworts such as Marchantia polymorpha and Lunularia cruciata produce small disc-shaped gemmae in shallow cups. Marchantia gemmae can be dispersed up to 120 cm by rain splashing into the cups. In Metzgeria, gemmae grow at thallus margins. Marchantia polymorpha is a common weed in greenhouses, often covering the entire surface of containers;: 230 gemma dispersal is the "primary mechanism by which liverwort spreads throughout a nursery or greenhouse.": 231
Thalloid liverworts typically harbor symbiotic glomeromycete fungi which have arbuscular (cilia-bearing) rootlets resembling those in vascular plants. Species in the Aneuraceae, however, associate with basidiomycete fungi belonging to the genus Tulasnella, while leafy liverworts typically harbor symbiotic basidiomycete fungi belonging to the genus Serendipita.
Today, liverworts can be found in many ecosystems across the planet except the sea and excessively dry environments, or those exposed to high levels of direct solar radiation. As with most groups of living plants, they are most common (both in numbers and species) in moist tropical areas. Liverworts are more commonly found in moderate to deep shade, though desert species may tolerate direct sunlight and periods of total desiccation.
Relationship to other plants
Traditionally, the liverworts were grouped together with other bryophytes (mosses and hornworts) in the Division Bryophyta, within which the liverworts made up the class Hepaticae (also called Marchantiopsida). Somewhat more recently, the liverworts were given their own division (Marchantiophyta), as bryophytes became considered to be paraphyletic. However, the most recent phylogenetic evidence indicates that liverworts are indeed likely part of a monophyletic clade ("Bryophyta sensu lato" or "Bryophyta Schimp.") alongside mosses and hornworts.[excessive citations] Hence, it has been suggested that the liverworts should be de-ranked to a class called Marchantiopsida. In addition, there is strong phylogenetic evidence to suggest that liverworts and mosses form a monophyletic subclade named Setaphyta.
|'Monophyletic bryophytes' model||'Liverworts plus mosses–basal' model|
|Two of the most likely models for bryophyte evolution.|
An important conclusion from these phylogenies is that the ancestral stomata appear to have been lost in the liverwort lineage. Among the earliest fossils believed to be liverworts are compression fossils of Pallaviciniites from the Upper Devonian of New York. These fossils resemble modern species in the Metzgeriales. Another Devonian fossil called Protosalvinia also looks like a liverwort, but its relationship to other plants is still uncertain, so it may not belong to the Marchantiophyta. In 2007, the oldest fossils assignable at that time to the liverworts were announced, Metzgeriothallus sharonae from the Givetian (Middle Devonian) of New York, United States. However, in 2010, five different types of fossilized liverwort spores were found in Argentina, dating to the much earlier Middle Ordovician, around 470 million years ago.
Bryologists classify liverworts in the division Marchantiophyta. This divisional name is based on the name of the most universally recognized liverwort genus Marchantia. In addition to this taxon-based name, the liverworts are often called Hepaticophyta. This name is derived from their common Latin name as Latin was the language in which botanists published their descriptions of species. This name has led to some confusion, partly because it appears to be a taxon-based name derived from the genus Hepatica which is actually a flowering plant of the buttercup family Ranunculaceae. In addition, the name Hepaticophyta is frequently misspelled in textbooks as Hepatophyta, which only adds to the confusion.
- The Jungermanniopsida includes the two orders Metzgeriales (simple thalloids) and Jungermanniales (leafy liverworts).
- The Marchantiopsida includes the three orders Marchantiales (complex-thallus liverworts), and Sphaerocarpales (bottle hepatics), as well as the Blasiales (previously placed among the Metzgeriales). It also includes the problematic genus Monoclea, which is sometimes placed in its own order Monocleales.
- A third class, the Haplomitriopsida is newly recognized as the sister group of the other liverworts; it comprises the genera Haplomitrium, Treubia, and Apotreubia.
|Forrest 2006||Cole, Hilger & Goffinet 2021 |
An updated classification by Söderström et al. 2016
- Marchantiophyta Stotler & Crandall-Stotler 2000
- Haplomitriopsida Stotler & Crandall-Stotler 1977
- Marchantiopsida Cronquist, Takhtajan & Zimmermann 1966
- Jungermanniopsida Stotler & Crandall-Stotler 1977
- Jungermanniidae Engler 1893 (leafy liverworts)
- Metzgeriidae Bartholomew-Began 1990
- Pelliidae He-Nygrén et al. 2006
It is estimated that there are about 9000 species of liverworts, at least 85% of which belong to the leafy group. Despite that fact, no liverwort genomes have been sequenced to date and only few genes identified and characterized.
In ancient times, it was believed that liverworts cured diseases of the liver, hence the name. In Old English, the word liverwort literally means liver plant. This probably stemmed from the superficial appearance of some thalloid liverworts which resemble a liver in outline, and led to the common name of the group as hepatics, from the Latin word hēpaticus for "belonging to the liver". An unrelated flowering plant, Hepatica, is sometimes also referred to as liverwort because it was once also used in treating diseases of the liver. This archaic relationship of plant form to function was based in the "Doctrine of Signatures".
Liverworts have little direct economic importance today. Their greatest impact is indirect, through the reduction of erosion along streambanks, their collection and retention of water in tropical forests, and the formation of soil crusts in deserts and polar regions However, a few species are used by humans directly. A few species, such as Riccia fluitans, are aquatic thallose liverworts sold for use in aquariums. Their thin, slender branches float on the water's surface and provide habitat for both small invertebrates and the fish that feed on them.
A small collection of images showing liverwort structure and diversity:
- Walker, Matt. "Fossils of earliest land plants discovered in Argentina" . (BBC, Earth News, 2010).
- Stotler, Raymond E.; Barbara J. Candall-Stotler (1977). "A checklist of the liverworts and hornworts of North America". The Bryologist. American Bryological and Lichenological Society. 80 (3): 405–428. doi:10.2307/3242017. JSTOR 3242017.
- Crandall-Stotler, Barbara; Stotler, Raymond E. (2000). "Morphology and classification of the Marchantiophyta". In A. Jonathan Shaw; Bernard Goffinet (eds.). Bryophyte Biology. Cambridge: Cambridge University Press. p. 21. ISBN 0-521-66097-1.
- Liverworts Homepage | UNB
- Schuster, Rudolf M. The Hepaticae and Anthocerotae of North America, volume VI, page 19. (Chicago: Field Museum of Natural History, 1992). ISBN 0-914868-21-7.
- Schuster, Rudolf M. The Hepaticae and Anthocerotae of North America, vol. I, pp. 243–244. (New York: Columbia University Press, 1966)
- Kashyap, Shiv Ram. Liverworts of the Western Himalayas and the Panjab Plain, vol. I, p. 1. (New Delhi: The Chronica Botanica, 1929)
- Schofield, W. B. Introduction to Bryology, pp. 135–140. (New York: Macmillan, 1985). ISBN 0-02-949660-8.
- Nehira, Kunito. "Spore Germination, Protonemata Development and Sporeling Development", p. 347 in Rudolf M. Schuster (Ed.), New Manual of Bryology, volume I. (Nichinan, Miyazaki, Japan: The Hattori Botanical Laboratory, 1983). ISBN 49381633045.
- Allison, K. W. & John Child. The Liverworts of New Zealand, pp. 13–14. (Dunedin: University of Otago Press, 1975).
- Conard, Henry S. and Paul L. Redfearn, Jr. How to Know the Mosses and Liverworts, revised ed., pp. 12–23. (Dubuque, Iowa: William C. Brown Co., 1979) ISBN 0-697-04768-7
- Harold C. Bold, C. J. Alexopoulos, and T. Delevoryas. Morphology of Plants and Fungi, 5th ed., p. 189. (New York: Harper-Collins, 1987). ISBN 0-06-040839-1.
- Volume 1, Chapter 11-1: Photosynthesis: The Process
- Fosket, Donald E. Plant Growth and Development: A Molecular Approach, p. 27. (San Diego: Academic Press, 1994). ISBN 0-12-262430-0.
- Hicks, Marie L. Guide to the Liverworts of North Carolina, p. 10. (Durham: Duke University Press, 1992). ISBN 0-8223-1175-5.
- Nehira, Kunito. "Spore Germination, Protonemata Development and Sporeling Development", pp. 358–374 in Rudolf M. Schuster (Ed.), New Manual of Bryology, volume I. (Nichinan, Miyazaki, Japan: The Hattori Botanical Laboratory, 1983). ISBN 49381633045.
- Chopra, R. N. & P. K. Kumra. Biology of Bryophytes, pp. 1–38. (New York: John Wiley & Sons, 1988). ISBN 0-470-21359-0.
- Malcolm, Bill & Nancy Malcolm. Mosses and Other Bryophytes: An Illustrated Glossary, pp. 6 & 128. (New Zealand: Micro-Optics Press, 2000). ISBN 0-473-06730-7.
- Campbell, Douglas H. The Structure and Development of Mosses and Ferns, pp. 73–74. (London: The Macmillan Co., 1918)
- Pain, S. (2010). "Botanical ballistics". New Scientist. 208 (2792/3): 45–47. doi:10.1016/s0262-4079(10)63177-6.
- Cooke, Todd J; Poli, DorothyBelle; Cohen, Jerry D (2003). "Did auxin play a crucial role in the evolution of novel body plans during the Late Silurian-Early Devonian radiation of land plants?". The Evolution of Plant Physiology. Elsevier. pp. 85–107. doi:10.1016/b978-012339552-8/50006-8. ISBN 978-0-12-339552-8.
- Friedman, William E.; Moore, Richard C.; Purugganan, Michael D. (2004). "The evolution of plant development". American Journal of Botany. Botanical Society of America (Wiley). 91 (10): 1726–1741. doi:10.3732/ajb.91.10.1726. ISSN 0002-9122. PMID 21652320.
- Lepp, Heino (15 April 2008). "Vegetative Reproduction". Australian Bryophytes. Australian National Botanic Gardens. Retrieved 22 December 2011.
- Smith, AJE (1989) The Liverworts of Britain and Ireland, Cambridge University Press, Cambridge.
- Equihua, C. (1987). "Splash-Cup Dispersal Of Gemmae In The Liverwort Marchantia-Polymorpha". Cryptogamie, Bryologie, Lichénologie. 8 (3): 199–217. Archived from the original on 26 April 2012.
- Lepp, Heino (28 February 2008). "Reproduction & Dispersal". Australian Bryophytes. Australian National Botanic Gardens. Retrieved 22 December 2011.
- Newby, Adam; Altland, James E.; Gilliam, Charles H.; Wehtje, Glenn (December 2006). "Postemergence Liverwort Control in Container-Grown Nursery Crops1" (PDF). J. Environ. Hort. Horticultural Research Institute. 24 (4): 230–236. Archived from the original (PDF) on 24 July 2012. Retrieved 24 December 2011.
- Bidartondo, Martin I.; Duckett, Jeffrey G. (7 February 2010). "Conservative ecological and evolutionary patterns in liverwort–fungal symbioses". Proceedings of the Royal Society B: Biological Sciences. 277 (1680): 485–492. doi:10.1098/rspb.2009.1458. PMC 2842645. PMID 19812075.
- Schuster, Rudolf M. The Hepaticae and Anthocerotae of North America, vol. I, pp. 243–249. (New York: Columbia University Press, 1966).
- Pócs, Tamás. "Tropical Forest Bryophytes", p. 59 in A. J. E. Smith (Ed.) Bryophyte Ecology. (London: Chapman and Hall, 1982). ISBN 0-412-22340-6.
- Crandall-Stotler, Barbara. & Stotler, Raymond E. "Morphology and classification of the Marchantiophyta". pp. 36–38 in A. Jonathan Shaw & Bernard Goffinet (Eds.), Bryophyte Biology. (Cambridge: Cambridge University Press: 2000). ISBN 0-521-66097-1
- Goffinet, Bernard. "Origin and phylogenetic relationships of bryophytes". pp. 124–149 in A. Jonathan Shaw & Bernard Goffinet (Eds.), Bryophyte Biology. (Cambridge: Cambridge University Press:!2000). ISBN 0-521-66097-1
- Cox, Cymon J.; et al. (2014). "Conflicting Phylogenies for Early Land Plants are Caused by Composition Biases among Synonymous Substitutions". Systematic Biology. 63 (2): 272–279. doi:10.1093/sysbio/syt109. PMC 3926305. PMID 24399481.
- Puttick, Mark N.; et al. (March 2018). "The Interrelationships of Land Plants and the Nature of the Ancestral Embryophyte". Current Biology. 28 (5): 733–745.e2. doi:10.1016/j.cub.2018.01.063. hdl:1983/ad32d4da-6cb3-4ed6-add2-2415f81b46da. PMID 29456145. S2CID 3269165.
- de Sousa, Filipe; et al. (2019). "Nuclear protein phylogenies support the monophyly of the three bryophyte groups (Bryophyta Schimp.)". New Phytologist. 222 (1): 565–575. doi:10.1111/nph.15587. hdl:1983/0b471d7e-ce54-4681-b791-1da305d9e53b. PMID 30411803. S2CID 53240320.
- Leebens-Mack, James H.; et al. (2019). "One thousand plant transcriptomes and the phylogenomics of green plants". Nature. 574 (7780): 679–685. doi:10.1038/s41586-019-1693-2. PMC 6872490. PMID 31645766.
- Zhang, Jian; et al. (2020). "The hornwort genome and early land plant evolution". Nature Plants. 6 (2): 107–118. doi:10.1038/s41477-019-0588-4. PMC 7027989. PMID 32042158.
- Harris, Brogan J.; et al. (2020). "Phylogenomic Evidence for the Monophyly of Bryophytes and the Reductive Evolution of Stomata". Current Biology. 30 (11): P2201–2012.E2. doi:10.1016/j.cub.2020.03.048. hdl:1983/fbf3f371-8085-4e76-9342-e3b326e69edd. PMID 32302587. S2CID 215798377.
- Li, Fay-Wei; et al. (2020). "Anthoceros genomes illuminate the origin of land plants and the unique biology of hornworts". Nature Plants. 6 (3): 259–272. doi:10.1038/s41477-020-0618-2. hdl:10261/234303. PMC 8075897. PMID 32170292.
- Sousa, Filipe; et al. (2020). "The Chloroplast Land Plant Phylogeny: Analyses Employing Better-Fitting Tree- and Site-Heterogeneous Composition Models". Frontiers in Plant Science. 11: 1062. doi:10.3389/fpls.2020.01062. PMC 7373204. PMID 32760416.
- Su, Danyan; et al. (2021). "Large-Scale Phylogenomic Analyses Reveal the Monophyly of Bryophytes and Neoproterozoic Origin of Land Plants". Molecular Biology and Evolution. 38 (8): 3332–3344. doi:10.1093/molbev/msab106. PMC 8321542. PMID 33871608.
- Sousa, Filipe; et al. (2020). "The mitochondrial phylogeny of land plants shows support for Setaphyta under composition-heterogeneous substitution models". PeerJ. 8 (4): e8995. doi:10.7717/peerj.8995. PMC 7194085. PMID 32377448.
- Cox, Cymon J. (2018). "Land Plant Molecular Phylogenetics: A Review with Comments on Evaluating Incongruence Among Phylogenies". Critical Reviews in Plant Sciences. 37 (2–3): 113–127. doi:10.1080/07352689.2018.1482443. hdl:10400.1/14557. S2CID 92198979.
- Taylor, Thomas N. & Edith L. Taylor. The Biology and Evolution of Fossil Plants, p. 139. (Englewood Cliffs, NJ: Prentice Hall, 1993). ISBN 0-13-651589-4.
- Oostendorp, Cora. The Bryophytes of the Palaeozoic and the Mesozoic, pp. 70–71. (Bryophytum Bibliotheca, Band 34, 1987). ISBN 3-443-62006-X.
- VanAller Hernick, L.; 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 (2–4): 154–162. doi:10.1016/j.revpalbo.2007.09.002.
- Rubinstein, C.V.; Gerrienne, P.; De La Puente, G.S.; Astini, R.A.; Steemans, P. (2010). "Early Middle Ordovician evidence for land plants in Argentina (eastern Gondwana)". New Phytologist. 188 (2): 365–369. doi:10.1111/j.1469-8137.2010.03433.x. PMID 20731783.
- Crandall-Stotler, Barbara. & Stotler, Raymond E. "Morphology and classification of the Marchantiophyta". p. 63 in A. Jonathan Shaw & Bernard Goffinet (Eds.), Bryophyte Biology. (Cambridge: Cambridge University Press:2000). ISBN 0-521-66097-1
- Jones, E. W. (2004). Liverwort and Hornwort Flora of West Africa. Scripta Botnica Belgica. Vol. 30. Meise: National Botanic Garden (Belgium). p. 30. ISBN 90-72619-61-7.
- Forrest, Laura L.; Christine E. Davis; David G. Long; Barbara J. Crandall-Stotler; Alexandra Clark; Michelle L. Hollingsworth (2006). "Unraveling the evolutionary history of the liverworts (Marchantiophyta): multiple taxa, genomes and analyses". The Bryologist. 109 (3): 303–334. doi:10.1639/0007-2745(2006)109[303:UTEHOT]2.0.CO;2. S2CID 85912159.
- Heinrichs, Jochen; S. Robbert Gradstein; Rosemary Wilson; Harald Schneider (2005). "Towards a natural classification of liverworts (Marchantiophyta) based on the chloroplast gene rbcL". Cryptogamie Bryologie. 26 (2): 131–150.
- He-Nygrén, Xiaolan; Aino Juslén; Inkeri Ahonen; David Glenny; Sinikka Piippo (2006). "Illuminating the evolutionary history of liverworts (Marchantiophyta) – towards a natural classification". Cladistics. 22 (1): 1–31. doi:10.1111/j.1096-0031.2006.00089.x. PMID 34892891. S2CID 86082381.
- Renzaglia, Karen S.; Scott Schuette; R. Joel Duff; Roberto Ligrone; A. Jonathan Shaw; Brent D. Mishler; Jeffrey G. Duckett (2007). "Bryophyte phylogeny: Advancing the molecular and morphological frontiers". The Bryologist. 110 (2): 179–213. doi:10.1639/0007-2745(2007)110[179:BPATMA]2.0.CO;2. S2CID 85788756.
- Forrest, Laura L.; Barbara J. Crandall-Stotler (2004). "A Phylogeny of the Simple Thalloid Liverworts (Jungermanniopsida, Metzgeriidae) as Inferred from Five Chloroplast Genes". Monographs in Systematic Botany. Molecular Systematics of Bryophytes. Missouri Botanical Garden Press. 98: 119–140.
- Schuster, Rudolf M. The Hepaticae and Anthocerotae of North America, vol. VI, p. 26. (Chicago: Field Museum of Natural History, 1992). ISBN 0-914868-21-7.
- Cole, Theodor C. H.; Hilger, Hartmut H.; Goffinet, Bernard. "Bryophyte phylogeny poster: systematics and Characteristics of Nonvascular Land Plants (Mosses, Liverworts, Hornworts)". 2021. Retrieved 6 December 2022.
- Söderström; et al. (2016). "World checklist of hornworts and liverworts". PhytoKeys (59): 1–826. doi:10.3897/phytokeys.59.6261. PMC 4758082. PMID 26929706.
- Sadava, David; David M. Hillis; H. Craig Heller; May Berenbaum (2009). Life: The Science of Biology (9th ed.). New York: W. H. Freeman. p. 599. ISBN 978-1429246446.
- Sierocka, I; Kozlowski, L. P.; Bujnicki, J. M.; Jarmolowski, A; Szweykowska-Kulinska, Z (2014). "Female-specific gene expression in dioecious liverwort Pellia endiviifolia is developmentally regulated and connected to archegonia production". BMC Plant Biology. 14: 168. doi:10.1186/1471-2229-14-168. PMC 4074843. PMID 24939387.
- Dittmer, Howard J. Phylogeny and Form in the Plant Kingdom, p. 286. (Toronto: D. Van Nostrand Co., 1964)
- Raven, P. H., R. F. Evert, & S. E. Eichhorn. Biology of Plants, 7th ed., p. 351. (New York: W. H. Freeman, 2005). ISBN 0-7167-1007-2.
- Stern, Kingsley R. Introductory Plant Biology, 5th ed., p. 338. (Dubuque, Iowa: Wm. C. Brown Publishers, 1991) ISBN 0-697-09947-4.
- Media related to Marchantiophyta at Wikimedia Commons
- Data related to Marchantiophyta at Wikispecies
- Liverwort structure in pictures
- LiToL: Assembling the Liverwort Tree of Life (note: for 500,000 million years ago read "480 million years ago".)
- Inter-relationships of Mosses, Liverworts, and Hornworts
- Additional information on Liverworts