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. 2014 Jan;113(1):35-54.
doi: 10.1093/aob/mct247. Epub 2013 Nov 5.

Stasis and convergence characterize morphological evolution in eupolypod II ferns

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Stasis and convergence characterize morphological evolution in eupolypod II ferns

Michael A Sundue et al. Ann Bot. 2014 Jan.

Abstract

Background and aims: Patterns of morphological evolution at levels above family rank remain underexplored in the ferns. The present study seeks to address this gap through analysis of 79 morphological characters for 81 taxa, including representatives of all ten families of eupolypod II ferns. Recent molecular phylogenetic studies demonstrate that the evolution of the large eupolypod II clade (which includes nearly one-third of extant fern species) features unexpected patterns. The traditional 'athyrioid' ferns are scattered across the phylogeny despite their apparent morphological cohesiveness, and mixed among these seemingly conservative taxa are morphologically dissimilar groups that lack any obvious features uniting them with their relatives. Maximum-likelihood and maximum-parsimony character optimizations are used to determine characters that unite the seemingly disparate groups, and to test whether the polyphyly of the traditional athyrioid ferns is due to evolutionary stasis (symplesiomorphy) or convergent evolution. The major events in eupolypod II character evolution are reviewed, and character and character state concepts are reappraised, as a basis for further inquiries into fern morphology.

Methods: Characters were scored from the literature, live plants and herbarium specimens, and optimized using maximum-parsimony and maximum-likelihood, onto a highly supported topology derived from maximum-likelihood and Bayesian analysis of molecular data. Phylogenetic signal of characters were tested for using randomization methods and fitdiscrete.

Key results: The majority of character state changes within the eupolypod II phylogeny occur at the family level or above. Relative branch lengths for the morphological data resemble those from molecular data and fit an ancient rapid radiation model (long branches subtended by very short backbone internodes), with few characters uniting the morphologically disparate clades. The traditional athyrioid ferns were circumscribed based upon a combination of symplesiomorphic and homoplastic characters. Petiole vasculature consisting of two bundles is ancestral for eupolypods II and a synapomorphy for eupolypods II under deltran optimization. Sori restricted to one side of the vein defines the recently recognized clade comprising Rhachidosoraceae through Aspleniaceae, and sori present on both sides of the vein is a synapomorphy for the Athyriaceae sensu stricto. The results indicate that a chromosome base number of x =41 is synapomorphic for all eupolypods, a clade that includes over two-thirds of extant fern species.

Conclusions: The integrated approach synthesizes morphological studies with current phylogenetic hypotheses and provides explicit statements of character evolution in the eupolypod II fern families. Strong character support is found for previously recognized clades, whereas few characters support previously unrecognized clades. Sorus position appears to be less complicated than previously hypothesized, and linear sori restricted to one side of the vein support the clade comprising Aspleniaceae, Diplaziopsidaceae, Hemidictyaceae and Rachidosoraceae - a lineage only recently identified. Despite x =41 being a frequent number among extant species, to our knowledge it has not previously been demonstrated as the ancestral state. This is the first synapomorphy proposed for the eupolypod clade, a lineage comprising 67 % of extant fern species. This study provides some of the first hypotheses of character evolution at the family level and above in light of recent phylogenetic results, and promotes further study in an area that remains open for original observation.

Keywords: Athyriaceae; Diplaziopsidaceae; Polypodiales; Rhachidosoraceae; Woodsiaceae; character state reconstruction; convergent evolution; eupolypods II; morphological evolution; rate of evolution; symplesiomorphy.

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Figures

Fig. 1.
Fig. 1.
Maximum-likelihood phylogram of the molecular dataset from Rothfels et al. (2012a, blue) compared with maximum-parsimony branch lengths of the morphological data set (orange). Letters A–G refer to clades cited in the text. Family names follow Rothfels et al. (2012b) (Onocleac. = Onocleaceae; H = Hemidictyaceae; Dipls = Diplaziopsidaceae; Rha = Rhachidosoraceae).
Fig. 2.
Fig. 2.
Morphological features in eupolypod II ferns. (A) Pale fleshy roots, Homalosorus pycnocarpos; (B) petiole base with two vascular bundles, Homalosorus pycnocarpos; (C) medial portion of petiole with two vascular bundles fused into an x-shape, Asplenium nidus (photo: Tom Ranker, used with permission); (D) trophopods, left arrow points to aborted leaf apex, right arrow points to thickened persistent starch-filled petiole base, Matteuccia struthiopteris; (E) pneumatophores, Deparia acrostichoides; (F) reddish young leaves, Salpichlaena volubilis; (G) anastomosing veins and membranaceous leaf margin, Hemidictyum marginatum; (H) pinna costae with adaxial projections, Athyrium microphyllum; (I) arrow points to whitish acicular hairs, Thelypteris supina.
Fig. 3.
Fig. 3.
Soral and indusial characters of eupolypod II ferns. (A) Round sori, Cystopteris fragilis; (B–F) elongate sori restricted to one side of the vein: (B) Homalosorus pycnocarpos; (C) Hemidictyummarginatum; (D) Hymenasplenium laetum; (E) Diplaziopsis javanica; (F) Blechnum orientale; (G–I) elongate sori along both sides of the vein: (G) Athyrium dolosum (=Deparia sect. Lunathyrium); (H) Diplazium riparium; (I) Athyrium niponicum.
Fig. 4.
Fig. 4.
Rachis–costa architecture in eupolypod II ferns. (A) Onoclea sensibilis; (B) Matteuccia struthiopteris; (C) Homalosorus pycnocarpos; (D) Diplazium assimile; (E) Deparia acrostichoides; (F) Athyrium japonicum; (G) Hymenasplenium riparium; (H) Asplenium harpeodes; (I) Asplenium uniseriale.
Fig. 5.
Fig. 5.
Ancestral state analysis for eupolypod II ferns. Branch colours depict maximum-parsimony optimization. Pie charts depict proportional likelihoods. (A) Character 74, mean number of annulus cells in the sporangia. (B) Character 75, chromosome base numbers.

References

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