Diplazium Sw., J. Bot. (Schrader) 1800

Kessler, Michael & Smith, Alan R., 2018, Prodromus of a fern flora for Bolivia. XXXII. Athyriaceae, Phytotaxa 334 (2), pp. 141-151 : 142-143

publication ID

https://doi.org/ 10.11646/phytotaxa.334.2.4

persistent identifier

https://treatment.plazi.org/id/F95A1307-FFD6-FF92-73C7-F95A5FD0D396

treatment provided by

Felipe

scientific name

Diplazium Sw., J. Bot. (Schrader) 1800
status

 

Diplazium Sw., J. Bot. (Schrader) 1800 View in CoL (2): 4, 61, 61. 1801.

Diplazium View in CoL comprises about 350–400 species, mainly in tropical regions, with probably over 150 species in the Neotropics; thirty species are known from Bolivia. The genus is characterized by its elongate, usually indusiate sori that are usually placed back-to-back (at least in larger or basal portions of ultimate segments) along the same vein (diplazioid sori), coarse roots, and two, laterally arranged, ribbon-like petiolar vascular bundles. A species group with rhizome scales bearing black, bifid, marginal teeth was segregated in the genus Callipteris ( Pacheco & Moran 1999) , but molecular studies show that this clade falls within Diplazium View in CoL ( Wang et al. 2002, Wei et al. 2013, 2015).

Diplazium View in CoL is often confused with Hymenasplenium ( Aspleniaceae View in CoL ), a few species of which may have diplazioid sori ( Smith 1976, Kessler & Smith 2017 b), but Diplazium View in CoL seldom has clathrate rhizome scales. Additionally, there are difficult-to-observe characteristics (number of annular cells, number of sporangial stalk cells, position of vascular bundles) separating these two genera. The monotypic genus Hemidictyum View in CoL (treated by us in Aspleniaceae View in CoL ; Kessler & Smith 2017 b) has historically sometimes been included in Diplazium View in CoL because of its linear, indusiate sori, but differs in having ±parallel veins that form a reticulate network of pentagonal or hexagonal areoles in the marginal half of the pinnae, also in having continuous intramarginal veins in each pinna; it also has a very different chromosome base number, x = 31. One other Bolivian species has also most often been regarded as belonging in Diplazium View in CoL Desmophlebium lechleri (Mett.) Mynssen et al. View in CoL ; this, and a related species, Diplazium longisorum (Baker) C.Chr. from Colombia, are now placed in a family Desmophlebiaceae View in CoL by Mynssen et al. (2016), but we prefer to subsume Desmophlebium View in CoL in more broadly defined family Aspleniaceae View in CoL (see Kessler & Smith 2017 b).

Because of its many species, large, often incompletely sampled fronds in herbaria, absence of modern monographic work, and lack of globally based phylogenetic studies that might provide a solid framework for regional floristic treatments, Diplazium View in CoL is still relatively poorly known, compared to many other fern genera. New species continue to be described (e.g., Adams 1992, Kessler & Smith 2007, Mynssen & Sylvestre 2013), and several species complexes would greatly benefit from thorough biosystematic study. Within Diplazium View in CoL , blade dissection is generally useful for species identification, but it is not necessarily an indicator of species relationships; juvenile, sterile specimens are often less dissected than adult, fertile forms. Affinities of species are more reliably assessed by characters of venation, indument, pinna and pinnule symmetry, and soriation ( Wei et al. 2013). Judging from chromosome counts of neotropical species, which range from diploid to octoploid ( Smith & Mickel 1977, Smith & Foster 1984), and from frequent intermediate specimens with malformed spores, hybridization may be common between neotropical species of Diplazium View in CoL (see, e.g., Stolze et al. 1994, Mickel & Smith 2004). In addition, agamospory has been documented in a few species ( Dopp 1932, Walker 1985).

In tropical America, Diplazium is a common genus on the forest floor, mainly at low- to mid-elevations ( Mickel & Smith 2004, Kessler et al. 2014). However, its evolutionary origin appears to lie in the northern hemisphere while this still had tropical climatic conditions in the Eocene ( Wei et al. 2015). It then migrated from Eurasia to North America over land bridges as a member of the boreotropical flora. In addition, there appears to have been long-distance dispersal events between Eurasia and tropical America. In Asia, species of Diplazium , in particular the aptly named D. esculentum (Retz.) Sw. , are commonly eaten as cooked vegetables.

Relatively modern floristic treatments of Diplazium in several neotropical countries and regions are available for Jamaica ( Proctor 1985), Puerto Rico ( Proctor 1989), and the Lesser Antilles ( Proctor 1977), Mexico ( Mickel & Smith 2004); Mesoamerica (Adams 1995); Ecuador ( Stolze et al. 1994), and Peru (Tryon & Stolze 1992).

Kingdom

Plantae

Phylum

Tracheophyta

Class

Polypodiopsida

Order

Polypodiales

Family

Athyriaceae

Loc

Diplazium Sw., J. Bot. (Schrader) 1800

Kessler, Michael & Smith, Alan R. 2018
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