Austronea phyllopogon Mart.-Azorín, M.Pinter, M.B.Crespo & M.Á.Alonso
publication ID |
https://doi.org/ 10.11646/phytotaxa.449.2.10 |
DOI |
https://doi.org/10.5281/zenodo.14205185 |
persistent identifier |
https://treatment.plazi.org/id/3D616226-A001-7A5D-10B7-F91CFAD6F8A4 |
treatment provided by |
Felipe |
scientific name |
Austronea phyllopogon Mart.-Azorín, M.Pinter, M.B.Crespo & M.Á.Alonso |
status |
sp. nov. |
Austronea phyllopogon Mart.-Azorín, M.Pinter, M.B.Crespo & M.Á.Alonso View in CoL , sp. nov. ( Fig. 1 View FIGURE 1 )
Austronea phyllopogon approaches A. barkerae in leaf morphology, but the former species produces fewer and narrower leaves in mature plants, has a denser indumentum, and presents a densely capitate inflorescence (not subcorymbose) comprising subsessile flowers (not long pedicellate) with smaller ovary.
Type:— SOUTH AFRICA. Northern Cape. Kamiesberg (3018): NE of Garies, Kamiesberg , ca 2 km NW of turn-off to Leliefontein from Studer’s Pass road, near farm house (−AC), 1123 m elevation, sandy soil, 11 April 2020 (in flower ex hort.), M. Martínez-Azorín, M.B. Crespo, M.Á. Alonso & M. Pinter MMA1817 b (holotype GRA , isotype ABH ).
Herbaceous deciduous geophyte. Bulb hypogeal, ovoid, 10−20 × 8−17 mm with a hypogeal neck 5−20 mm long, solitary, with compact, white, thickened, scales, and pale brown, membranous to papery outer tunics. Roots fleshy, white, branched, 8−30 × 0.5−1 mm. Leaves 3−5, proteranthous and mostly withered at flowering time, hypogeal portion 3−13 mm long, aerial portion 12−25 × 1.2−2.2 mm, spreading and appressed to the ground, narrowly linear-lanceolate, with the widest portion along the distal third, slightly fleshy-succulent, flattened and slightly canaliculated, rounded abaxially, dull greyish green, covered with abundant white, spreading to slightly retrorse hairs of 0.4−0.8 mm long along the margins and abaxial side, sometimes less profuse adaxially. Inflorescence nodding in bud, raceme ca 2 mm long, capitate or subglobose, with 3−5, nearly sessile flowers; peduncle at anthesis 10−14 cm long, greyish, erect or flexuose, glabrous, smooth, papillate along the basal half; pedicels shorter than 1 mm long at anthesis, spreading, smooth; bracts ovate-lanceolate, 0.8−1.0 mm long, clasping the pedicels, the lowermost with broad, papery, reddish spurs with white membranous margin, ca 1.5 mm long, clasping the peduncle. Flowers pentacyclic, trimerous, stellate, opening about noon and withering in the night, 1−2 flowers open at a time, flower buds reddish; tepals 6, entire, reddish (‘burnt orange’), with a darker longitudinal central band on the abaxial side, slightly glandulous at the apex, biseriate, outer overlapping inner at the base, connate at the base for ca 1 mm to form a distinct cup, free portions patent to slightly reflexed; outer tepals ovate, ca 4 × 1.5 mm, with strongly revolute margins; inner tepals ovate-lanceolate, 3.8 × 1.5 mm, with slightly revolute margins. Stamens 6, erect, adnate to perigone for ca 0.5 mm; filaments white, fleshy, narrowly lanceolate, flat, ca 1.5 × 0.4 mm, smooth; anthers yellow, oblong, ca 0.5 mm long, dehiscing by longitudinal slits, with yellow pollen. Ovary green to orange, oblong, truncate to the style, ca 1.5 × 1.2 mm; style white, columnar, erect, ca 1.4 mm long, trigonous in transverse section; stigma small, glandulose and slightly papillate. Capsules and seeds not studied.
Etymology:—Named after the distinctly hairy leaves, the diagnostic character of the species (from the Greek words “φύλλον” [phyllon: leaf] and “πώγων” [pogon: beard, hairs]).
Phenology: — Austronea phyllopogon flowers around April in cultivation in the northern hemisphere. Flowers are shortlived, lasting less than a day and withering during the night.
Habitat: —This species is restricted to the Fynbos Biome and occurs in deep sandy soil in FRg1 Namaqualand Granite Renosterveld. It is characterized by a mean annual precipitation from 130 to 370 mm (mean: 235 mm), peaking from May to August, a mean annual temperature of ca 14 ºC and 10−30 days of frost incidence per year ( Mucina & Rutherford 2006).
Distribution:— Austronea phyllopogon is only known from one population SE of Leliefontein in the Kamiesberg, Northern Cape Province of South Africa. Further research is needed to evaluate its real extension range, especially considering its cryptic appearance.
Diagnostic characters and taxonomic relationships:— Austronea phyllopogon is identified by the solitary bulb, the 3−5 proteranthous, narrowly linear-lanceolate, appressed leaves covered with abundant white, spreading to slightly retrorse hairs of 0.4−0.8 mm long, the capitate inflorescence with nearly sessile flowers and the small ovary. Austronea phyllopogon shares hairy or ciliate leaves with A. barkerae (Oberm. ex Manning & Goldblatt 2003:109) Mart. -Azorín et al. (2018: 107), A. ciliolata (J.C.Manning & J.M.J.Deacon in Manning & Goldblatt 2018: 89) Mart.-Azorín et al. (2019b: 293), A. fimbrimarginata (Snijman in Snijman & Harrower 2009: 234) Martínez-Azorín et al. (2018: 108), A. hispidoplicata Martínez-Azorín et al. (2018: 114) and A. olifanta Martínez-Azorín et al. (2018: 119) , though those latter species differ by leaf size, morphology and indumentum in combination with inflorescence and flower morphology ( Martínez-Azorín et al. 2018). The morphologically closest relatives appear to be A. barkerae and A. olifanta , using the identification key in Martínez-Azorín et al. (2018), but both latter species present broader and more numerous leaves in mature plants together with lax indumentum, and long pedicellate flowers with longer ovaries. They further occur in different habitats that are restricted to the surroundings of Piketberg and Clanwilliam respectively. Austronea phyllopogon also resembles A. pygmaea ( Duthie 1928: 10) Martínez-Azorín et al. (2018: 108) , A. chalumnesis ( Dold & Brink 2004: 631) Martínez-Azorín et al. (2018: 107) or A. patersoniae Martínez-Azorín et al. (2019a: 77) based on leaf morphology, although the latter species do not exhibit hairs but rather only minute papillae; their different inflorescences and flower morphologies further distinguish them (cf. Martínez-Azorín et al. 2018).
Additional material studied (paratypes):— SOUTH AFRICA. Northern Cape. Kamiesberg (3018): NE of Garies, Kamiesberg, ca. 2 km NW of turn-off to Leliefontein from Studer’s Pass road, near farm house (−AC), 1123 m elevation, sandy soil, 21 August 2017 (in leaf), M. Martínez-Azorín, M.B. Crespo, M.Á. Alonso & M. Pinter MMA1817 a ( ABH!) .
GRA |
GRA |
ABH |
ABH |
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