Correlates of monoicy and dioicy in hornworts, the apparent sister group to vascular plants
© Villarreal and Renner; licensee BioMed Central Ltd. 2013
Received: 4 July 2013
Accepted: 16 October 2013
Published: 2 November 2013
Whether male and female gametes are produced by single or separate individuals shapes plant mating and hence patterns of genetic diversity among and within populations. Haploid-dominant plants (“bryophytes”: liverworts, mosses and hornworts) can have unisexual (dioicous) or bisexual (monoicous) gametophytes, and today, 68% of liverwort species, 57% of moss species, and 40% of hornwort species are dioicous. The transitions between the two sexual systems and possible correlations with other traits have been studied in liverworts and mosses, but not hornworts. Here we use a phylogeny for 98 of the 200 species of hornworts, the sister group to vascular plants, representing roughly equal proportions of all monoicous and all dioicous species, to test whether transitions in sexual systems are predominantly from monoicy to dioicy as might be expected based on studies of mosses. We further investigate possible correlations between sexual system and spore size, antheridium number, ploidy level, and diversification rate, with character selection partly based on findings in mosses and liverworts.
Hornworts underwent numerous transitions between monoicy and dioicy. The transition rate from dioicy to monoicy was 2× higher than in the opposite direction, but monoicous groups have higher extinction rates; diversification rates do not correlate with sexual system. A correlation important in mosses, that between monoicy and polyploidy, apparently plays a small role: of 20 species with chromosome counts, only one is polyploid, the monoicous Anthoceros punctatus. A contingency test revealed that transitions to dioicy were more likely in species with small spores, supporting the hypothesis that small but numerous spores may be advantageous for dioicous species that depend on dense carpets of gametophytes for reproductive assurance. However, we found no evidence for increased antheridium-per-chamber numbers in dioicous species.
Sexual systems in hornworts are labile, and the higher number of extant monoicous species (60%) may be largely due to frequent transitions to monoicy.
KeywordsChromosome counts Sexual systems Spore size Trait correlation
Among the striking evolutionary changes along the phylogeny of embryophytes (Figure 1) is how the distribution of sexual systems changes between hornworts and vascular plants, their apparent sister group , partly because of the repeated evolution of heterospory, which entails sexually specialized gametophytes. Hornworts have 60% monoicous species and 40% dioicous ones, frequencies resembling those in liverworts and mosses, but the situation is completely different in ferns and fern-like lineages. In spite of their pivotal phylogenetic position, the evolution of monoicy and dioicy in hornworts has never been analyzed, probably because of the lack of a phylogenetic framework and outdated information on the presence or absence of monoicy and dioicy in the various genera. The directionality of change between monoicy and dioicy is therefore unknown. Here we use a modern hornwort phylogeny, based on plastid and mitochondrial loci and comprising 98 of the 200 species, and original data on the occurrence of monoicy and dioicy in the different species, to infer the minimal number of switches between monoicy and dioicy in this clade. We also test whether correlations between these two sexual systems and certain traits that have been detected in studies of liverworts and mosses, hold true in hornworts. We explain the background for these correlations in the next sections.
Sexual reproduction in dioicous hornworts, as in liverworts and mosses, depends on the availability of water and short distances between antheridia and archegonia, which is required for the motile sperm to fertilize the egg. Hornworts with separate-sexed gametophytes may therefore have a less assured reproduction than hornworts with cosexual gametophytes. However, intra-gametophyte mating is equivalent to the most extreme form of selfing, resulting in 100% homozygous progeny in a single generation. There is some evidence for selfing in monoicous mosses [9–11], but no data are available for hornworts. In spite of these expectations, monoicy and dioicy occur in roughly equal proportion in all three haploid-dominant embryophyte lineages (Figure 1). This raises the question of whether other traits precondition a lineage towards one of the two sexual systems. For example, in mosses, there appears to be a correlation between dioicy and small spores . This became apparent in an analysis that used grafted phylogenies (: Additional file 1: Table S1) to look at correlations between sexual system, spore size, seta length, and polyploidy. (Since the phylogeny was grafted, Crawford et al.  only analyzed correlations but did not infer the evolutionary direction of sexual system transitions). Dioicous mosses were more likely to have small spores if spore size was coded as a discrete character, but not if it was coded as a continuous character. The underlying cause of the possible correlation between spore size and monoicy was seen in the greater dispersal distance of small spores compared to large spores, which would compensate for higher local extinction rates of dioicous species (because of reproductive failure when sperm cannot reach egg cells).
In hornworts, spore sizes range from 18 μm diameter in Leiosporoceros up to >100 μm in the multicellular spores of Dendroceros. If small spores are cheaper to produce than large ones they can be produced in larger numbers, which might be especially advantageous in dioicous species for which a dense spore shadow and dense population of gametophytes might provide reproductive assurance (because sperm would not have to swim far). The antheridia and archegonia of hornworts are embedded inside the thallus, and antheridium number varies from one up to 80 per chamber, with fairly narrow species-specific ranges [13, 14]. Excluding possible animal vectors (such as mites), the flagellate sperm cells travel only a few centimeters [14–16]. Our initial expectation therefore was that dioicous hornworts would produce not only small spores, but also a higher number of antheridia per chamber than monoicous species to be able to produce more numerous sperm, again for reproductive assurance.
Besides testing for correlations between sexual system, spore diameter, and/or antheridium number, we were interested in whether there might be a correlation between polyploidy and sexual system. Hornworts usually have a low number of chromosomes, typically n = 5 (4 + U/V, the presumed sex chromosomes) in dioicous species and n = 5–6 in monoicous species, with few polyploid species . Polyploidy is extremely rare in liverworts [18, 19], but in mosses, polyploidy is common, and polyploid species tend to be monoicous ([2, 12, 20], and references therein). This is expected because following autopolyploidy, random pairing of the sex chromosomes will lead to both dioicous and monoicous offspring (depending on chromosome segregation), while following allopolyploidy, there will be only monoicous progeny, since after homeologous pairing each spore will contain a U chromosome and a V chromosome [2, 20, 21].
The species included in our phylum-wide phylogeny were selected to represent monoicous and dioicous species more or less in the proportion found across all hornworts, so as best to be able to answer the following questions: (i) Is dioicy or monoicy the more likely sexual system during the early phase of hornwort evolution? (ii) To what extent are shifts in sexual system correlated with shifts in spore size, antheridium number, and/or polyploidy? And (iii) is dioicy associated with lower diversification rates?
Taxon sampling, isolation of DNA, amplification, and sequencing
We sampled 98 of the 200 species of hornworts; Additional file 1: Table S1 provides a list of the sampled species with taxonomic author names, herbarium vouchers, and GenBank accession numbers for all sequences. Determination of plant material relied mostly on comparison with type material, but five of the sampled species are not yet formally described.
DNA isolation followed standard protocols. To deduce phylogenetic relationships we used the mitochondrial nad5-exon2, excluding an intron of ~950 nucleotides that is unique to Leiosporoceros, Anthoceros, Folioceros and Sphaerosporoceros the plastid gene rbcL and portions of the trnK intron and the matK gene contained within it (primers designed by Alan Forrest, Royal Botanical Garden Edinburgh). Total DNA from fresh, silica-dried or herbarium material was extracted with the Nucleo-Spin plant kit according to the manufacturer’s protocol (Macherey–Nagel, Düren, Germany). Primers and standard PCR protocols are listed in  except primers newly designed for matKa. PCR products were cleaned using ExoSap-it (Affymetrix, Santa Clara, CA, USA), and sequencing reactions using Big Dye version 3.1 were run on an ABI 3130 capillary sequencer (Applied Biosystems, Perkin-Elmer, Wellesley, MA, USA), following manufacturers’ protocols. Sequence editing and alignment were carried out in Sequencher 4.7 (Gene Codes, Ann Arbor, MI, USA) and Geneious v. 5.6.6.
Combined phylogenetic analyses were performed under likelihood (ML) optimization and the GTR + G substitution model, using RAxML  with 500 bootstrap replicates. Bayesian analyses were conducted in MrBayes v. 3.2 , using the default two runs and four chains (one cold and three heated), with uniform priors on most parameters. Model parameters were unlinked, posterior probabilities of tree topologies were estimated from both partitions (the plastid and the mitochondrial data), and trees were sampled every 10000th generation. Burn-in and convergence were assessed using Tracer v. 1.5 . Convergence was usually achieved after 4 × 106 generations. We used 50% majority rule consensus trees to assess posterior probabilities for nodes of interest, and the 5000 trees with the highest likelihood were used for ancestral reconstructions. All analyses were run using the Cipres Science Gateway servers .
Ancestral character reconstruction and correlated trait analyses
The sexual system (dioicous, state 0, or monoicous, state 1) of each species was scored from the literature or personal observations [28–33]. Sixty-five of the ~ 110 known monoicous species were sampled (~60%), and 33 of 54 known dioicous species (~61%). Trees were rooted on Leiosporoceros, the sole genus of the Leiosporocerotaceae, which based on outgroup-rooting is sister to all other hornworts . This was preferable to outgroup comparison because two of the traits that we scored lack homologues in the vascular plants: Spore diameter (small, <35 μm, state 0, or large, >35 μm, 1) and antheridium number per chamber (low, <9, state 0, or high, >10, 1). Average mature spore diameters were taken from relevant literature [28–33]. The third trait, chromosome number, was taken from [34, 35] and mapped onto the phylogeny.
Ancestral reconstruction relied on ML as implemented in Mesquite using the Markov 1- or 2- parameter models  and the highest likelihood tree from RAxML. To test the null hypothesis of equal transition frequencies between the two sexual systems, we performed a likelihood ratio test (LRT) that compared the likelihood of a 1-parameter model of equal transition rates (called q) with a 2-parameter, asymmetric model, which allows separate rates of transitions to monoicy and to dioicy . Test significance was evaluated based on a χ2 distribution with 1 degree of freedom. We also reconstructed the ancestral conditions of spore size and antheridium number using a 1-parameter model or a 2-parameter model.
Character state-associated diversification
The diversification rate associated with each character state and the transition rates between character states have an impact on the distribution of binary traits [39, 40]. We used the binary-state speciation and extinction (BiSSE) modelling approach to estimate transition rates among character states and character-associated diversification rates [39, 40]. Our dataset includes 27 to 100% of the extant species in each of the hornwort genera (all of which have more than one species); sparse species sampling is a problem for all diversification modelling, and is also a problem in the present study. BiSSE model analyses were carried out in Mesquite using the diversitreeRpackage (http://www.zoology.ubc.ca/prog/diversitree/).
Results and discussion
The combined plastid and mitochondrial alignment had 3593 nucleotide positions of which the matK gene and portions of the trnK intron comprised 700–1000 positions; we excluded the intron in the nad5 gene (Additional file 2: Matrix S1). Topologies from the individual partitions were congruent for most clades, although with less resolution in the tree obtained from the slow evolving nad5 alone. A ML tree from the combined data matrix has solid bootstrap support for most major hornwort clades except Phaeomegaceros, and its topology is consistent with previous phylogenetic reconstructions except for two novel findings: The nested position of Folioceros and Sphaerosporoceros within Anthoceros and the placement of two species of Paraphymatoceros (P. hallii and the type of the genus name, P. diadematus) as a clade nested within Phaeoceros along with the Californian P. pearsonii and P. proskauerii (Figure 2B). Megaceros minarum is embedded in Nothoceros, and the species will need to be transferred to that genus.
Figure 1 shows the distribution of the four basic sexual systems in embryophytes, namely dioicy/monoicy in haploid-dominants and dioecy/monoecy in diploid-dominant lineages (cf. Introduction). The evolution of heterospory in some ferns and the ancestor of all seed plants led to exclusively unisexual gametophytes, the ecological role of which is completely different from that of the free-living unisexual or bisexual gametophytes of the three haploid-dominant plant lineages. If early-diverging ferns and fern-like lineages had monoicous gametophytes, then the ancestral condition in hornwort gametophytes probably also was monoicous. The ancestral condition of the hornwort sporophyte is clear: All hornworts, ferns, and lycophytes have monoecious sporophytes.
Reconstruction of trait evolution using a maximum likelihood approach
- log-likelihood- 1-rate
- log-likelihood- 2-rate
Large (>35 μm) (1)
1-9 per chamber (0)
More than 10 (1)
Likelihood ratio values for analyses of trait correlation
Change to large spores conditional upon sexual system state
Change to small spores conditional upon sexual system state
Change to monoicy conditional upon spore size state
Change to dioicy conditional upon spore size state
q12 = q34
q21 = q43
q13 = q24
q31 = q42
q21 = 19.56
q13 = 277.5
q31 = 199.72
q43 = 45.59
q24 = 35.18
q42 = 11.93
Bias in the estimation of transition rates in sexual systems is introduced when the sexual systems experience different rates of diversification [39, 40]. Our BiSSE analyses, however, showed that while the transition rate from dioicy to monoicy was 4.2 higher than vice versa (q01 = 120.00; q10 = 28.17), the speciation rates in monoicous and dioicous clades were similar (λ0 = 265.34; λ1 = 275.93). Monoicous groups accordingly had a higher extinction rate (μ0 = 182.49; μ1 = 294.11). The slightly higher number of extant monoicous species (60% vs. 40% dioicous species) may thus be entirely due to frequent transitions to monoicy.
In species with genetic sex determination, transition to monoicy may follow genome duplication, because genome doubling may disrupt the strict segregation of the male and female sex chromosomes (Introduction). Only twenty species of hornworts have had their chromosomes counted, some repeatedly, resulting in 65 counts [34, 35]. Sixteen of the twenty species are represented in our phylogeny (Additional file 3: Figure S1). So far, a single natural polyploid has been reported, the monoicous Anthoceros punctatus. This fits the expected association of monoicy and polyploidy, but is insufficient to decide whether such an association holds across hornworts.
Our finding that lineages with small spores transition to dioicy more readily than those with large spores matches the situation in mosses, although in that clade this was only true if spore diameter was coded as a discrete character, but not when it was coded as a continuous character . Crawford et al.  argued that evolutionary transitions to separate sexes might be easier if sporophytes produce small spores that might travel further. However, release height and wind speed probably override the importance of spore diameter in determining dispersal range , and it is also unclear why further dispersal might be more beneficial for dioicous species than monoicous ones. In hornworts, the sporophytes elongate by means of a basal meristem, with mature sporangium length varying from 2–3 mm in some species of Notothylas to >10 centimeters in species of Anthoceros, Megaceros, and Nothoceros. A more plausible explanation for the correlation between having small spores and transition to dioicy therefore is a resource allocation trade-off, such that larger numbers of spores can only be produced when each spore has a small diameter. Once a lineage has small spores, this may facilitate its transition to separate sexes because female thalli producing more numerous spores create a denser spore shadow, permitting sperm to more easily reach thalli of the opposite sex. Data on spore number per capsule so far are only available for Anthoceros agrestis (with large spores) , and experiments are required to test the above-proposed hypothesis.
In monoicous species of hornworts, the antheridia tend to develop earlier than the archegonia , minimizing intra-gametophyte fertilization and perhaps reducing inbreeding and the accompanying selection for dioicy. Lastly and importantly, our study of sexual system switches in hornworts, together with the data on such switches available for liverworts [18, 19] and mosses [43, 44], makes clear that suggestions of dioicy being ancestral in “bryophytes” (at the time assumed to be a monophylum) and of monoicy being the derived sexual system  need to be put to rest. Instead, sexual systems in the three lineages of haploid-dominant land plants are highly labile, and there is no single preferential direction. Given the under-sampling in all phylogenies used in studies of sexual system evolution to date, back and forth transitions between dioicy and monoicy probably are still underestimated. Quantitative and experimental studies of the apparent trade-off between spore diameter, spore number, and spore shadows are much needed.
A phylogeny for 98 of the 200 species of hornworts, representing roughly equal proportions of their monoicous and dioicous species, implies many shifts between monoicy and dioicy, terms that refer to the sexual systems of haploid tissues (compare Figure 1 for the distribution of the four main sexual systems in land plants). Different from mosses, the transition rate from dioicy to monoicy in hornworts exceeds that in the opposite direction, while diversification rates do not differ with sexual system. Trait correlation analyses revealed that transitions to dioicy are more likely in species with small spores, while the opposite is not the case. If smaller spores can be produced in larger numbers, smaller-spored species may enjoy denser spore shadows, ensuring successful fertilization because of shorter distances between male and female gametophytes. However, we found no evidence of increased antheridium-per-chamber numbers in dioicous species. A correlation between monoicy and polyploidy apparently plays a small role in hornworts.
We thank, D. C. Cargill (Australian National Herbarium, CANB), S. Chantanaorrapint (Songkla University, Thailand), B. Goffinet (University of Connecticut), K. Hylander (Stockholm University), T. Peng and R.-L. Zhu (Herbaria of East China Normal University), S. Pressel and J.G. Duckett (Natural History Museum, London), J. Shevock (California Academy of Sciences), and H. Stieperaere (National Botanical Garden of Belgium for plant material; D. C. Cargill for a sequences of A. fragilis; L. L. Forrest and A. Forrest (Royal Botanical Garden Edinburgh) for the matK primer and laboratory support, and N. Cusimano in our lab in Munich for providing an R script for Figure 1. Three anonymous reviewers provided constructive comments that improved the manuscript. Financial support came from the DFG grant RE-603/14-1 and SYNTHESYS GB-TAF-1893.
- Bateman R, DiMichelle WA: Heterospory: the most iterative innovation in the evolutionary history of the plant kingdom. Biol Rev. 1994, 69: 345-417. 10.1111/j.1469-185X.1994.tb01276.x.View ArticleGoogle Scholar
- Wyatt R, Anderson LE: Breeding systems in bryophytes. The experimental biology of bryophytes. Edited by: Dyer AF, Duckett JG. 1984, London: Academic, 39-64.Google Scholar
- Frey W, Stech M: Marchantiophyta, Bryophyta, Anthocerotophyta. Syllabus of Plant Families - Engler’s Syllabus der Pflanzenfamilien, 13ed. Part 3: Bryophytes and seedless Vascular Plants. Edited by: Frey W. 2009, Berlin: Borntraeger, 13-115.Google Scholar
- Von Konrat M, Söderström L, Renner MAM, Hagborg A, Briscoe L, Engel JJ: Early land plants today (ELPT): how many liverwort species are there?. Phytotaxa. 2010, 9: 22-40.View ArticleGoogle Scholar
- Magill RE: Moss diversity: new look at old numbers. Phytotaxa. 2010, 9: 167-174.View ArticleGoogle Scholar
- Smith A, Pryer KM, Schuettpelz E, Korall P, Schneider H, Wolf PG: A classification for extant ferns. Taxon. 2006, 55: 705-731. 10.2307/25065646.View ArticleGoogle Scholar
- Renner SS, Ricklefs RE: Dioecy and its correlates in the flowering plants. Am J Bot. 1995, 82: 596-606. 10.2307/2445418.View ArticleGoogle Scholar
- Qiu Y, Li L, Wang B, Chen Z, Knoop V, et al: The deepest divergences in land plants inferred from phylogenomic evidence. Proc Natl Acad Sci USA. 2006, 103: 15511-15516. 10.1073/pnas.0603335103.PubMed CentralPubMedView ArticleGoogle Scholar
- Taylor PJ, Eppley SM, Jesson LK: Sporophytic inbreeding depression in mosses occurs in species with separate sexes but not in a species with combined sexes. Am J Bot. 2007, 94: 1856-1859.View ArticleGoogle Scholar
- Eppley SM, Taylor PJ, Jesson KL: Self-fertilization in mosses: a comparison of heterozygote deficiency between species with combined versus separate sexes. Heredity. 2007, 98: 38-44. 10.1038/sj.hdy.6800900.PubMedView ArticleGoogle Scholar
- Perroud PF, Cove DJ, Quatrano RS, McDaniel SF: An experimental method to facilitate the identification of hybrid sporophytes in the moss Physcomitrella patens using fluorescence tagged lines. New Phytol. 2011, 191: 301-306. 10.1111/j.1469-8137.2011.03668.x.PubMed CentralPubMedView ArticleGoogle Scholar
- Crawford M, Jesson LK, Garnock-Jones PJ: Correlated evolution of sexual system and life-history traits in mosses. Evolution. 2009, 63: 1129-1142. 10.1111/j.1558-5646.2009.00615.x.PubMedView ArticleGoogle Scholar
- Renzaglia KS, Villarreal JC, Duff RJ: New insights into morphology, anatomy and systematics of hornworts. Bryophyte Biology II. Edited by: Goffinet B, Shaw AJ. 2009, Cambridge: University Press, 139-171.Google Scholar
- Proskauer J: Studies on the morphology of Anthoceros I. Ann Bot. 1948, 12: 237-265.Google Scholar
- Cronberg N, Natcheva R, Hedlund K: Microarthropods mediate sperm transfer in mosses. Science. 2006, 313: 1255-10.1126/science.1128707.PubMedView ArticleGoogle Scholar
- Rosenstiel RN, Shortlidge EE, Melnychenko AN, Pankow JF, Eppley SM: Sex-specific volatile compounds influence microarthropod-mediated fertilization of moss. Nature. 2012, 489: 431-433. 10.1038/nature11330.PubMedView ArticleGoogle Scholar
- Proskauer J: Studies on Anthocerotales V. Phytomorphology. 1957, 7: 113-135.Google Scholar
- Devos N, Renner MAM, Gradstein SR, Shaw AJ, Laenen B, Vanderpoorten A: Evolutionary significance and trade-offs in life history traits associated to ecological specialization and mating systems in the liverwort genus Radula. New Phytol. 2011, 192: 225-236. 10.1111/j.1469-8137.2011.03783.x.PubMedView ArticleGoogle Scholar
- Bainard JD, Forrest LL, Goffinet B, Newmaster SG: Nuclear DNA content variation and evolution in liverworts. Mol Phyl Evol. 2013, 68: 619-627. 10.1016/j.ympev.2013.04.008.View ArticleGoogle Scholar
- Såstad SM: Patterns and mechanisms of polyploid speciation in bryophytes. Regnum Vegetabile. 2005, 143: 317-334.Google Scholar
- Bachtrog D, Kirkpatrick M, Mank JE, McDaniel SF, Pires JC, Rice WR, Valenzuela N: Are all sex chromosomes created equal?. Trends Genet. 2011, 27: 350-357. 10.1016/j.tig.2011.05.005.PubMedView ArticleGoogle Scholar
- Duff RJ, Villarreal JC, Cargill DC, Renzaglia KS: Progress and challenges toward developing a phylogeny and classification of the hornworts. Bryologist. 2007, 110: 214-243. 10.1639/0007-2745(2007)110[214:PACTDA]2.0.CO;2.View ArticleGoogle Scholar
- Villarreal JC, Renner SS: Hornwort pyrenoids, a carbon-concentrating mechanism, evolved and were lost at least five times during the last 100 million years. Proc Natl Acad Sci USA. 2012, 109: 18873-18878. 10.1073/pnas.1213498109.PubMed CentralPubMedView ArticleGoogle Scholar
- Stamatakis A, Hoover P, Rougemont J: A rapid bootstrap algorithm for the RAxML Web-servers. Syst Biol. 2008, 75: 758-771. 10.1080/10635150802429642.View ArticleGoogle Scholar
- Ronquist F, Teslenko M, Van der Mark P, Ayres DL, Darling A, Höhna S, Larget B, Liu L, Suchard MA, Huelsenbeck JP: MrBayes 3.2: efficient Bayesian phylogenetic inference and model choice across a large model space. Syst Biol. 2012, 61: 539-542. 10.1093/sysbio/sys029.PubMed CentralPubMedView ArticleGoogle Scholar
- Rambaut A, Drummond AJ: Tracer v. 1.5. 2007, Available from [http://beast.bio.ed.ac.uk/Tracer]
- Miller MA, Pfeiffer W, Schwartz T: Creating the CIPRES Science Gateway for inference of large phylogenetic trees. 2010, New Orleans: Proceedings of the Gateway Computing Environments Workshop (GCE), 1-8. 14 Nov. 2010Google Scholar
- Asthana AK, Srivastava SC: Indian hornworts (a taxonomic study). Bryophyt Bibl. 1991, 42: 1-158.Google Scholar
- Cargill DC, Fuhrer BA: Taxonomic studies of the Australian Anthocerotophyta II: the genus Phaeoceros. Fieldiana Bot. 2008, 47: 239-253. 10.3158/0015-0746-47.1.239.View ArticleGoogle Scholar
- Crandall-Stotler BJ, Stotler RE, Doyle WT, Forrest LL: Phaeoceros proskauerii sp. nov., a new species of the Phaeoceros hallii (Aust.) Prosk.- Phaeoceros pearsoniii (M. Howe) Prosk. complex and the systematic affinities of Paraphymatoceros Hässel. Fieldiana, Bot. 2008, 47: 213-238. 10.3158/0015-0746-47.1.213.View ArticleGoogle Scholar
- Chantanaorrapint S: Phaeoceros perpusillus (Notothyladaceae), a new species of hornwort from Thailand. Acta Bot Hungarica. 2009, 51: 29-33. 10.1556/ABot.51.2009.1-2.6.View ArticleGoogle Scholar
- de Menéndez GG: Las especies de Phaeoceros (Anthocerotophyta) de América del Norte, Sud y Central; la ornamentación de sus esporas y taxonomía. Candollea. 1989, 44: 717-739.Google Scholar
- Peng T, Zhu RL: A revision of the genus Anthoceros (Anthocerotaceae, Anthocerotophyta) in China. Phytotaxa. 2013, 100: 21-35. 10.11646/phytotaxa.100.1.3.View ArticleGoogle Scholar
- Fritsch R: Index to bryophyte chromosome counts. Bryophyt Bibl. 1991, 40: 1-352.Google Scholar
- Przywara L, Kuta E: Karyology of bryophytes. Polish Bot Studies. 1995, 9: 1-83.Google Scholar
- Maddison WP, Maddison DR: Mesquite: a modular system for evolutionary analysis, version 2.73. 2010, Available at http://mesquiteproject.org
- Pagel M: The maximum likelihood approach to reconstructing ancestral character states of discrete characters on phylogenies. Syst Biol. 1999, 48: 612-622. 10.1080/106351599260184.View ArticleGoogle Scholar
- Pagel M: Detecting correlated evolution on phylogenies: a general method for the comparative analysis of discrete characters. Proc R Soc Lond B Biol Sci. 1994, 255: 37-45. 10.1098/rspb.1994.0006.View ArticleGoogle Scholar
- Maddison WP, Midford PE, Otto SP: Estimating a binary character’s effect on speciation and extinction. Syst Biol. 2007, 56: 701-710. 10.1080/10635150701607033.PubMedView ArticleGoogle Scholar
- FitzJohn RG, Maddison WP, Otto SP: Estimating trait-dependent speciation and extinction rates from incompletely resolved phylogenies. Syst Biol. 2009, 58: 595-611. 10.1093/sysbio/syp067.PubMedView ArticleGoogle Scholar
- Lönnell N, Hylander K, Jonsson BG, Sundberg S: The fate of the missing spores — patterns of realized dispersal beyond the closest vicinity of a sporulating moss. PLoS One. 2012, 7: e41987-10.1371/journal.pone.0041987.PubMed CentralPubMedView ArticleGoogle Scholar
- Bisang I: An estimate of mature spore production in Anthoceros agrestis in Switzerland. J Bryol. 2001, 23: 142-145.Google Scholar
- McDaniel SF, Perroud J-P: Invited perspective: bryophytes as models for understanding the evolution of sexual systems. Bryologist. 2012, 115: 1-11. 10.1639/0007-2745-115.1.1.View ArticleGoogle Scholar
- McDaniel SF, Atwood J, Burleigh JG: Recurrent evolution of dioecy in bryophytes. Evolution. 2013, 67: 567-572. 10.1111/j.1558-5646.2012.01808.x.PubMedView ArticleGoogle Scholar
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