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237 results for “Asphodelaceae”
FIGURE 5 in Aloe davyana var. magdae (Asphodelaceae subfam. Alooideae), a distinctive new variety from central-northeastern South Africa
FIGURE 5. In this colony of Aloe davyana var. davyana growing near Pretoria, Gauteng province, South Africa, flower colour varies from flesh pink to dull brick red. Photograph: Gideon F. Smith.
FIGURE 6 in Aloe davyana var. magdae (Asphodelaceae subfam. Alooideae), a distinctive new variety from central-northeastern South Africa
FIGURE 6. Aloe davyana var. subolifera forms large clumps of up to 20 rosettes, and its flowers vary in colour from dusty pink, as here near Pienaarsrivier, Limpopo province, South Africa, to nearly white. Photograph: Gideon F. Smith.
FIGURE 1. A. Aloe verecunda has a in Aloe hankeyi (Asphodelaceae subfam. Alooideae; Aloe sect. Leptoaloe), a new species from northern South Africa
FIGURE 1. A. Aloe verecunda has a wide but patchy natural geographical distribution range in northeastern South Africa. This photograph of a form with bright red flowers was taken in the North West province near the western limits of its range. B. A. cooperi growing in dense grassland near Melmoth in KwaZulu-Natal, South Africa. Note the distinctly conical inflorescences and sparsely arranged sterile bracts higher up on the peduncles. C. A large clump of A. hankeyi in full flower. D. Leaves of A. hankeyi are not keeled, unlike those of A. cooperi, which are distinctly keeled abaxially. E. Racemes of A. hankeyi are broadly conical to distinctly flat-topped. F. The sterile peduncular bracts of A. hankeyi (peduncle on the left) are much more densely concentrated towards the raceme than in A. cooperi (peduncle on the right) or A. verecunda. G. The large flowers of A. hankeyi are dull red for ⅔ of their length, with the upper ⅓ being greenish. H. Andrew John Hankey (1968–) on 21 August 2019. I. Type locality of A. hankeyi (red dot). Unvouchered site records in eastern Gauteng and western Mpumalanga are not reflected on the map. All photographs by Gideon F. Smith.
FIGURE 5 in Pollen micromorphology and ultrastructure on four genera from Asphodelaceae and their taxonomical implication
FIGURE 5. Dendrogram was obtained from the analysis of pollen grain data in the studied species and their related taxonomic relationships. Three types showed in the dendrogram: Type 1 (Aloe- Eremurus type or node 6), type 2 (Asphodelus type or node 7), and type 3 (Hemerocallis type or node 8).
FIGURE 4 in Pollen micromorphology and ultrastructure on four genera from Asphodelaceae and their taxonomical implication
FIGURE 4. Transmission electron microscopic micrographs from Aloe vera (A. section of the whole pollen grain, B. pollen grain wall, and C. the pollen grain wall in the sulcus margin region) and Eremurus spectabilis (D. section of the whole pollen grain, E. pollen grain wall, F. the pollen grain wall in the sulcus margin region). F (Foot layer), C (Columellae), T (Tectum), E (Ectexine), In (Intine), and Io (Intine layer in the sulcus region). Scale bars—4 μm (A), 10 μm (D), 1 μm (E and F), and 0.5 μm (B and C).
FIGURE 3 in Pollen micromorphology and ultrastructure on four genera from Asphodelaceae and their taxonomical implication
FIGURE 3. Scanning electron microscopy micrographs from the pollen grains; Eremurus persicus (A–C), Eremurus spectabilis (D–F), Eremurus stenophylus (G–I), Hemerocallis minor (J–L). Scale bars—10 μm (A, D, G, J, M), 2 μm (B, E, H, K, N), and 5 μm (C, F, I, L, O). Bars = 10 μm for pollens (A, D, G, J, M), 2 μm for central and sulcus margin regions of pollens (B, E, H, K, N), and 5 μm for distal region of pollens (C, F, I, L, O).
FIGURE 1 in Pollen micromorphology and ultrastructure on four genera from Asphodelaceae and their taxonomical implication
FIGURE 1. Light microscopic photographs of the pollen grains; Aloe vera (A), Asphodelus tenuifolius (B), Eremurus inderiensis (C), Eremurus kopet-daghensis (D), Eremurus luteus (E), Eremurus persicus (F), Eremurus spectabilis (G), Eremurus stenophylus (H), and Hemerocallis minor (I). Scale bars—10 μm
FIGURE 2 in Pollen micromorphology and ultrastructure on four genera from Asphodelaceae and their taxonomical implication
FIGURE 2. Scanning electron microscopy micrographs of the pollen grains; Aloe vera (A–C), Asphodelus tenuifolius (D–F), Eremurus inderiensis (G–I), Eremurus kopet-daghensis (J–L), and Eremurus luteus (M–O). Scale bars—10 μm for pollens (A, D, G, J, M), 2 μm for central and sulcus margin regions of the pollens (B, E, H, K, N) and 5 μm for distal region of pollens (C, F, I, L, O).
FIGURE 6 in Pollen micromorphology and ultrastructure on four genera from Asphodelaceae and their taxonomical implication
FIGURE 6. Principal components analysis scatterplot obtained from overlapping of species (case scores) and pollen grain characters (variable loadings) (A); the situation of variable loadings from both axes (B). Type 1 (Aloe- Eremurus type); type 2 (Asphodelus type); type 3 (Hemerocallis type). Group A: P/E ratio, pollen shape, pollen type, exine ornamentation in central region, sulcus margin exine ornamentation, exine ornamentation in distal region, exine ornamentation in lumina region, minimum and maximum of lumina and muri size; Group B: minimum of equatorial and polar of pollens, average and maximum of polar from pollens; Ex: maximum of equatorial axis; and Em: average of the equatorial axis.
FIGURE 8 in Reinstatement of Aloe longibracteata (Asphodelaceae subfam. Alooideae), a maculate aloe from northeastern South Africa
FIGURE 8. The fruit of Aloe longibracteata, illustrated here, is larger than those of A. davyana. The dimensions of the bottom-most capsule in the photograph are 32 × 18 mm. Photograph: Gideon F. Smith.
FIGURE 6 in Reinstatement of Aloe longibracteata (Asphodelaceae subfam. Alooideae), a maculate aloe from northeastern South Africa
FIGURE 6. The inflorescences of Aloe longibracteata are often cat tail-like curved. Photograph: Gideon F. Smith.
FIGURE 5 in Reinstatement of Aloe longibracteata (Asphodelaceae subfam. Alooideae), a maculate aloe from northeastern South Africa
FIGURE 5. In developing inflorescences, including in the younger, fire scorched one, the long bracts for which the species was named, are very prominent. Photograph: Gideon F. Smith.
FIGURE 2 in Reinstatement of Aloe longibracteata (Asphodelaceae subfam. Alooideae), a maculate aloe from northeastern South Africa
FIGURE 2. Aloe davyana var. davyana generally has pale flesh-pink to dull brick-red flowers. Rosettes usually grow in small clusters. Photograph: Gideon F. Smith.
FIGURE 1 in Reinstatement of Aloe longibracteata (Asphodelaceae subfam. Alooideae), a maculate aloe from northeastern South Africa
FIGURE 1. Aloe longibracteata usually grows in the often dense, fire-prone grass and forb layer in savanna vegetation or on rocky outcrops as solitary to sparsely (1- or 2-)branched rosettes. The rosettes mostly produce up to 4-branched inflorescences per flowering season. Photograph: Gideon F. Smith.
FIGURE 4 in Reinstatement of Aloe longibracteata (Asphodelaceae subfam. Alooideae), a maculate aloe from northeastern South Africa
FIGURE 4. The abaxial leaf surfaces of Aloe longibracteata are light green to yellowish green. Plants usually grow as solitary rosettes. Photograph: Gideon F. Smith.
FIGURE 7 in Reinstatement of Aloe longibracteata (Asphodelaceae subfam. Alooideae), a maculate aloe from northeastern South Africa
FIGURE 7. The flowers of Aloe longibracteata are ± uniformly shiny strawberry-pink to peach-red in the lower ½, with the mouth slightly paler. Photograph: Gideon F. Smith.
FIGURE 2. A in Reinstatement of Aloe mutans (Asphodelaceae subfam. Alooideae), a distinctive, endemic, maculate aloe from the central Limpopo province of South Africa
FIGURE 2. A two-headed specimen of a form of Aloe davyana [var. davyana] with pale flesh-pink, greenish to greyish white-striped flowers. Photograph taken between Donkerhoek and Pretoria, Gauteng province, South Africa, by Gideon F. Smith. Note that each rosette has produced two inflorescences.
FIGURE 3 in Reinstatement of Aloe mutans (Asphodelaceae subfam. Alooideae), a distinctive, endemic, maculate aloe from the central Limpopo province of South Africa
FIGURE 3. Aloe mutans growing near Morotse in South Africa's Limpopo province. A. A solitary specimen. B. A two-headed specimen showing the brownish to yellowish green adaxial leaf surface. C. Solitary and multi-headed specimens, some of which are in flower while others are already in fruit. D. The leaf sap dries dark purplish. Abaxially the leaves are uniformly light green to greyish green; longitudinally indistinctly dark green-lined; and sometimes obscurely white-spotted, as here. E. Plants often grow in the shade of lowgrowing shrubs and small trees that act as nurse plants with only the inflorescences protruding above the shrub layer. F. The apicaL ⅓ to ½ of the perianth is yellow, which transitions through orange to strawberry pink basally. The basal swelling of the flowers is longitudinally more abruptly flattened than in A. davyana. All photographs by Gideon F. Smith.
FIGURE 4 in Reinstatement of Aloe mutans (Asphodelaceae subfam. Alooideae), a distinctive, endemic, maculate aloe from the central Limpopo province of South Africa
FIGURE 4. Aloe davyana growing near Pretoria, Gauteng province, South Africa. A. A three-headed specimen, with each rosette simultaneously producing two inflorescences. B. A form with uniformly dull brick-red flowers. C. Two flower colour forms (dull brickred on the left and pale flesh-pink on the right) growing in close proximity. D. The flowers are uniformly chromatic, not multi-coloured as in A. mutans. All photographs by Gideon F. Smith.
FIGURE 7. Kniphofia princeae. A. Inflorescence. B in A new species of Kniphofia (Asphodelaceae) from Nyungwe National Park, Rwanda
FIGURE 7. Kniphofia princeae. A. Inflorescence. B. Detail of infructescence with mature capsules. Kniphofia vandeweghei. C–D. Inflorescence. E. Peduncle with bracts and pedicels. F. Mature capsule. G. Detail of infructescence. Photographs: A–B. R. v. Blittersdorf, A. 31 March 2009, B. 14 February 2012, Tanzania, Sumbawanga, Mbizi Forest (see Blittersdorf 2009–2012). C–G. E. Fischer & M. Ackermann, Rwanda, Rwasenkoko swamp, 06 January 2018.
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