2017
DOI: 10.3897/phytokeys.83.13490
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Recircumscription and taxonomic revision of Siderasis, with comments on the systematics of subtribe Dichorisandrinae (Commelinaceae)

Abstract: A new circumscription and a total of six microendemic species, four of them new to science, are herein presented for Siderasis, based on field and herbaria studies, and cultivated material. We provide an identification key to the species and a distribution map, description, comments, conservation assessment, and illustration for each species. Also, we present an emended key to the genera of subtribe Dichorisandrinae, and comments on the morphology and systematics of the subtribe.

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Cited by 9 publications
(25 citation statements)
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“…observ. ), with Tradescantiazanonia (L.) Sw. (Commelinaceae) being an exception (Pellegrini 2017b; Pellegrini and Faden 2017). In Pontederiaceae, the anthocarp seems to be related to hydrochoric dispersion, which is also supported by the remaining synapomorphies for the family (i.e.…”
Section: Discussionmentioning
confidence: 99%
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“…observ. ), with Tradescantiazanonia (L.) Sw. (Commelinaceae) being an exception (Pellegrini 2017b; Pellegrini and Faden 2017). In Pontederiaceae, the anthocarp seems to be related to hydrochoric dispersion, which is also supported by the remaining synapomorphies for the family (i.e.…”
Section: Discussionmentioning
confidence: 99%
“…In Hanguanaceae, the fruits consist of variously coloured berries that detach from the persistent sepaloid perianth and are most probably zoochoric (Bayer et al 1998). On the other hand, in Commelinaceae, the fruits are primarily dehiscent capsules (rarely indehiscent capsules or berries), that do not rely on the persistent sepals for dispersion, with fruits or seeds being autochoric or more rarely zoochoric (Pellegrini and Faden 2017). …”
Section: Discussionmentioning
confidence: 99%
“…Indeed, a great deal of variation is observed in the family as a whole, with some patterns characteristic or synapomorphic to several taxonomic ranks (Brückner 1930; Handlos 1975; Hunt 1983; Faden 1991, 1998; Faden and Hunt 1991; Pellegrini et al 2016; Pellegrini and Faden 2017). The androecium morphology of Commelinaceae is known to vary regarding the: (1) symmetry of the androecium as a whole; (2) number of stamens; (3) fertility of the stamens; (4) similarity between the inner and outer whorl of stamens; (5) similarity within each whorl of stamens; (6) connation with the corolla; (7) filament connation; (8) position, curvature and torsion of the filaments; (9) pubescence of the filaments; (10) insertion of the anthers; (11) morphology of the connectives; (12) morphology of the anther sacs; (13) relative position of the anther sacs; (15) dehiscence of the anther sacs; and (16) fertility of the pollen grains (Faden 1998; Evans et al 2000, 2003; pers.…”
Section: Discussionmentioning
confidence: 99%
“…This is not surprising, considering that all Commelinaceae lack nectaries of all types, and pollen is the only floral resource available for pollinators (Faden 1992, 2000). Thus, it should be expected for androecium morphology to be strongly connected to key shifts in pollination syndromes in different lineages of the family (Faden 1992, 2000; Pellegrini and Faden 2017). …”
Section: Discussionmentioning
confidence: 99%
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