(Last Modified On 6/6/2016)
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Acceptance
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Accepted
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(Last Modified On 6/16/2016)
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Description:
Plants (50–)80–140 mm high. Corm bell-shaped, ± 10 mm diam.; tunics light red-brown, lightly ridged, basal margin entire or bluntly lobed. Stem simple or 1–few-branched from near base, slightly compressed. Leaves 4 or 5, lowermost longest, up to 160 mm long, linear to lanceolate, 2–6 mm wide, strongly ribbed, upper leaves shorter and broader, becoming progressively bract-like above. Inflorescences 6–20-flowered spikes, initially 2-ranked, later becoming spiral; outer bracts green, firm, ± succulent, 10–20 mm long, channeled, ovate when flattened, obtuse in side view (deltoid and retuse when unfolded), apex deflexed in profile, margins hyaline; inner bracts 1/3 to 1/2 as long, transparent with 2 green keels. Flowers zygomorphic, either white to pale mauve, pale blue or pale pink, lower tepals each with a small triangular to diamond-shaped median mark in lower half (subsp. pyramidalis) or violet, purple or dark carmine, lower tepals each with white or cream markings near base and a central zone of darker pigment (subsp. regalis), either intensely sweet scented day and night (subsp. pyramidalis) or evidently scentless (subsp. regalis); perianth tube 25–55 mm long, slender, straight or widening slightly in upper 5 mm; tepals subequal, narrowly to broadly ovate, narrowed into claw-like base ± 1.5 mm long, lower tepals each occasionally with a small claw-like cusp near base, dorsal tepal 9–15 × 6–7 mm, erect, held apart from others, upper lateral tepals slightly reflexed, lower 3 tepals usually held closely together and at right angles to tube, 8 × 5 mm. Stamens unilateral, ± erect to ascending; filaments 5–6 mm long, exserted ± 3.5 mm; anthers ± 3 mm long, usually pale yellow to white; pollen ± white. Style dividing between base and apex of anthers or slightly beyond; branches ± 2.5 mm long, forked for 1/2 their length, often becoming tangled in anthers. Capsules obovoid, 8–10 mm long, with wing-like locular ridges in distal half. Seeds ± globose to ovoid, usually somewhat flattened at chalazal end, 1.3–1.5 × 1.4–1.9 mm, epidermal cells tuberculate. Chromosome number 2n = 18. Flowering time: July to September.
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South African Province:
Northern Cape, Western Cape
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Distribution and ecology:
one of the more widespread species of the genus, extending from the southern edge of Namaqualand though dry areas of the northwestern Cape in Northern Cape to interior and southern Western Cape and Little Karoo and southern Cape; mostly on clay slopes and flats.
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Diagnosis:
Lapeirousia pyramidalis can always be immediately recognized by the broadly ovate to deltoid bracts with obtuse to retuse apices combined with a relatively long perianth tube 25–55 mm long. In profile the bracts do not taper to a point but curve outward and have blunt tips. The flowers have shortly clawed, subequal tepals with broadly oval to rounded limbs resembling the Namaqualand species, L. silenoides and we consider the two to be closely allied. Both also have unusual capsules with prominent ridges on the locules and similar red-brown corms with a ridged or lobed basal margin, features also shared with the local Namaqualand endemic, L. verecunda. The tuberculate seeds of L. pyramidalis are unusual in Lapeirousia, in which most species of sect. Chasmatocallis, including those of L. silenoides and L. verecunda, have epidermal cells with evenly domed (colliculate) outer walls. The difference is often striking, making it possible to distinguish the seeds of L. pyramidalis immediately from other species of the genus.
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General Notes:
Over much of its range Lapeirousia pyramidalis has a fairly consistent appearance. Plants are compact with broadly obtuse floral bracts, and the flowers are white to pale blue or pale pink to lilac with a perianth tube 25–35 mm long, slightly curved and wider in the upper 5–7 mm, and always strongly scented, both during the day and in the evening. In the west of its range, in the Olifants and Biedouw River valleys, and at Karoo Poort to the south, plants segregated as subsp. regalis are distinguished by bright red, purple, or dark violet flowers with a long, nearly straight perianth tube, 35–55 mm long, and have no discernable odour. As far as known, the two never grow sympatrically but their ranges are more or less complementary. They also favour different habitats: subsp. pyramidalis normally grows on shale and clay soils, but subsp. regalis has only been recorded on stony sandstone ground. There is also a marked size difference between the seeds of the two subspecies. Over much of its range subsp. pyramidalis has seeds 1.7–2.0 mm diam., but subsp. regalis has seeds ± 1/2 this size, 1.0–1.2 mm diam. The floral differences between the two subspecies reflect a shift in pollination strategy. Strongly scented subsp. pyramidalis is thought to be pollinated primarily by sphinx moths, which are most active at sunset and at night, whereas subsp. regalis is pollinated by long-proboscid flies.
Lapeirousia pyramidalis has a somewhat confused taxonomic history. The species was described by the French biologist, J.P.B. Lamarck in 1789, based on a collection attributed to the botanist, Philibert Commerson (1725–1773), but probably collected by his colleague, Pierre Sonnerat. Plants cultivated in Vienna were described as Gladiolus fissifolius by N.J. Jacquin in 1791, and the fine illustration published shortly thereafter shows this clearly to be the same as Lamarck’s species. For over 150 years the species was known by the later epithet, L. fissifolia and only after 1971 as L. pyramidalis.
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Specimens whose coordinates are enclosed in square brackets [ ] have been mapped to a standard reference mark based on political
units.
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Africa & Madagascar
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South Africa
:
1000 ft,
[28°34'22"S 023°49'34"E],
J.F. Drège 2641b
(MO)
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South Africa
:
1000 ft,
[28°34'22"S 023°49'34"E],
J.F. Drège 8508
(MO)
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South Africa
Western Cape:
21 July 1976,
Peter Goldblatt 3636
(MO)
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South Africa
Western Cape:
07 August 1976,
Peter Goldblatt 3822
(MO)
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South Africa
Western Cape:
12 August 1976,
Peter Goldblatt 3837
(MO)
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South Africa
Western Cape:
16 August 1976,
Peter Goldblatt 3914
(MO)
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South Africa
Western Cape:
17 September 1978,
Peter Goldblatt 4889
(MO)
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South Africa
Cape:
5 September 1991,
Peter Goldblatt 9196
(MO)
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South Africa
Cape:
17 September 1991,
Peter Goldblatt 9223
(MO)
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South Africa
Cape:
27 August 1991,
Peter Goldblatt & John C. Manning 9123
(MO)
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South Africa
Cape:
18 August 1993,
Peter Goldblatt & John C. Manning 9592
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South Africa
:
[28°34'22"S 023°49'34"E],
29 July 1994,
Peter Goldblatt & John C. Manning 9889
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South Africa
:
[28°34'22"S 023°49'34"E],
11 August 1994,
Peter Goldblatt & John C. Manning 9920
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South Africa
:
[28°34'22"S 023°49'34"E],
2 September 1994,
Peter Goldblatt & John C. Manning 9960
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South Africa
Western Cape:
28 August 2001,
Peter Goldblatt & Lendon J. Porter 11789
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South Africa
Western Cape:
15 September 2001,
Peter Goldblatt & Lendon J. Porter 11889
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South Africa
Western Cape:
16 September 2001,
Peter Goldblatt & Lendon J. Porter 11890
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South Africa
Western Cape:
12 August 2002,
Peter Goldblatt & Lendon J. Porter 12027
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South Africa
Western Cape:
12 August 2002,
Peter Goldblatt & Lendon J. Porter 12032
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South Africa
Western Cape:
10 September 2002,
Peter Goldblatt & Lendon J. Porter 12189
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South Africa
Western Cape:
2700 f,
33°09'55"S 020°09'59"E,
31 Aug 2007,
Peter Goldblatt & Lendon J. Porter 12932
(MO)
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South Africa
Western Cape:
2297 f,
33°09'41"S 019°45'02"E,
9 Sept 2007,
Peter Goldblatt & Lendon J. Porter 12971
(MO)
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South Africa
Western Cape:
23 Aug 2007,
Peter Goldblatt, John C. Manning & Lendon J. Porter 12856
(MO)
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