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Tuber 9-12 cm in diameter, light brown and somewhat ringleted, partly with buds; roots 5-8 mm thick, brownish yellow.
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Tuber 9-12 cm in diameter, light brown and somewhat ringleted, partly with buds; roots 5-8 mm thick, brownish yellow. LEAVES: Cataphylls 5-6, the first ones the shortest, more or less triangular, membrana-ceous, soon drying, 1.5-29 cm long, at the base (1) 2-2.5 cm wide, slightly reddish and a little spotted, the veins stronger colored. Petiole 1-1.3 m long, below 1-1.4 cm in diameter, spiny, spotted (more or less dark green olive and spotted with small yellowish white points); spines 1-2 mm long. Leaf blade divided in three main parts, each segment 30-35 cm long; rhachis more or less reddish, round below and flattened on upper side, its margins prominent; venation reticulate, veins underneath reddish, otherwise dark green; leaflets (4) 8-23 cm long and (2) 3-7 (11) cm wide, upper surface dark green with a blue grey touch, more or less shiny, apex truncate ending in two (0.5) 1-3 cm long acuminate to caudate side tips; the lowest leaflets ovate and cuspidate, 4.5-8 cm long and 2-5.5 cm wide. INFRUCTESCENCE: Peduncle short, yellowish, (3) 5-9 cm long and 1-1.5 cm in diameter, spiny, green or light purplish with greenish white roundish to elongate spots, spines 1-2 mm long and greenish white; cataphylls together with the inflorescence of the same size and color as those with the leaf. Spathe (30) 40-55 cm long, below for a length of 20-25 cm involute to a tube, fleshy and to 5 mm thick, above arched over and thin, more or less mem-branaceous, broad-pointed, margin slightly undulate; spathe outside greenish yellow, above getting a slight purplish touch; veins very prominent; inside below in the center deep purple, in the middle going over in a purple especially the veins, above greenish yellow (mostly the margin parts). Spadix more or less sessile, cylindric, blunt, fertile to its apex, (6) 9-12.5 cm long and (1.5) 2-2.5 cm in diameter; female part 2-3.5 (4) cm long; male part (3.5) 6-8.5 cm long. Pistil ca. 5 mm high; ovary globular to ellipsoid, somewhat squeezed, 2-3 mm in diameter, yellowish-whitish, bilocular, seldom trilocular, with one ovule in each locule, fixed at the base of the middle septum and ascending; ovule anatropous, ellipsoid, ca. 0.7 mm long and ca. 0.4 mm in diameter, funiculus ca. 0.5 mm long; style short, 1-1.5 mm long and ca. 1.5 mm in diameter, of the same color as the ovary; stigma bilobed, seldom trilobed, papillose, depressed in the center, ca. 2 mm in diameter, reddish brown to purple. Stamens free, ca. 4 mm high and rectangular in cross section, ca. 1.8 (2) x 1.2 mm, slightly angled, yellowish and at its top purple; thecae oblong, ca. 3 mm long and opening by an apical pore; connective capitate and rising above the thecae; pollen yellow and excuded in strings, pollen grain ellipsoid, inaperturate, 100-120u x 70-100u, exine slightly scabrous. INFRUCTESCENCE: unknown. Pollination: I collected as pollinators two different flies and two different beetles of the following families: Diptera: Choridae, Sphaeroceridae and Coleoptera: Scaphidiidae, Staphylinidae. They are normally found on rotten organic matter.
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Pseudohydrosme gabunensis, commonly known as the Gabon false hydrosme, is a species of flowering plant in the family Araceae. It was described by Heinrich Gustav Adolf Engler in 1892.
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Terrestrial herb, rhizome light brown, ellipsoid or subcylindric, erect or oblique, 9 – 12 cm diam. to 15 cm long, surface with transverse ridges. Roots fleshy 5 – 8 mm thick, brownish yellow, sometimes developing new plants at their tips (Hetterscheid & Bogner, 2013). Leaf 1 – 1.3 (– 2.2) m tall, petiole terete, 1 – 1.4 cm diam. at base, dark green olive and spotted, with small yellowish white points; prickles 1 – 2 mm long. Blade of youngest seedlings sagittate-elliptic c. 5 cm long, 3 – 4 cm wide, basal sinus c. 2 cm long, breadth variable (see Hetterscheid & Bogner, 2013). Successively formed blades developing slits and divisions. Blade of mature leaves dracontoid, primary divisions 30 – 35 cm long, pinnatisect, lobes in each division 5 – 8, dimorphic, larger, distal lobes elliptic (4 –) 8 – 23 cm long, (2 –) 3 – 7 (– 11) cm, apex truncate, bifid, (0.5 –) 1 – 3 cm long; smaller, proximal leaflets ovate, 4.5 – 8 cm long, 2.5 – 5 cm wide, apex cuspidate; lateral veins 4 – 8 on each side of the midrib, conspicuous on abaxial surface, running to the margin or forming an incomplete submarginal nerve, higher order veins reticulate. Inflorescence: Cataphylls 4 – 6, membranous, reddish white or brown-purple, slightly spotted, phyllotaxy spiral, proximal ones subtriangular shorter, distal ones becoming longer and oblong elliptic, towards the spathe 1.5 – 29 cm long, (1 –) 2 – 2.5 cm wide; peduncle (3 –) 5 – 9 cm long, 1 – 1.5 cm diam., colour as petiole, with minute sparse greenish white prickles 1 – 2 mm long. Spathe (30 –) 40 – 55 (– 70) cm long, fornicate, basal half (20 – 25 cm long) funnel-shaped to subcylindrical, fleshy and to 5 mm thick, limb comprising the distal half of the spathe, flaring widely and curving forward, the apex obtuse, margin undulate; outer surface uniform bright pale yellow, greenish yellow or yellow white; inner surface of blade mostly pale yellow or yellowish white, in an irregular marginal band, with a dark purple central area separated by an irregular margin down to the base of the tube; mouth facing horizontally, usually orbicular or elliptic. Spadix with “ unpleasant smell, but not so strong as some Araceae ” (Van der Laan 7641, WAG) or “ faintly of lettuce ” (Hetterscheid & Bogner (2013)) or “ of slightly bad cabbage ” (David Prehsler, University of Vienna communication to Cheek November 2020), sessile, subcylindrical, (6 –) 9 – 12.5 cm long, (1.5 –) 2 – 2.5 cm diam. Female zone (2 –) 3.5 (– 4) cm long, female flowers completely covering the surface of the axis, usually contiguous with but constricted at the junction with the male zone. Male zone (3.5 –) 6 – 8.5 cm long, at base abruptly wider than the female zone, tapering to the rounded apex, completely covered in fertile male flowers. Sterile appendix absent. Male flowers with 2 – 5 stamens, stamens densely packed, sometimes paired or in groups of 3 or 5, sessile, 4 mm long, in plan view isodiametric, subprismatic, 5 – 6 - faceted, in cross section c. 1.8 (– 2) mm × 1.2 mm wide, apex convex purple, sides white, anther thecae c. 3 mm long, opening by an apical pore, pollen orange or yellow, in strings. Female flowers white with ovary yellowish-white globose or ellipsoid, 2 – 3 mm diam., 2 (– 3) - locular; style 1 – 1.5 mm long, 1.5 mm diam., stigma black to reddish brown, surface papillose, 2 mm wide, bilobed, lobes with a broad concave area, apex rounded. Berry, thinly fleshy, transversely ellipsoid, laterally compressed, rarely globose, 0.8 – 1.2 cm long, 1.5 – 1.6 cm wide, white, ripening purple-black, surface wrinkled when ripe, style and stigma persistent, (1 –) 2 - seeded, apex rounded-truncate, base stipitate, stipes (2 –) 3 – 4 mm long, c. 2 mm diam. Seeds subglobose to broadly ellipsoid, one side flattened, the other convex, 9 mm long, 7 mm wide. Phenology: flowering in the wild mid-September – late October.
Pseudohydrosme gabunensis on average reaches about 15 cm (5.9 in) tall, and 9–12 cm (3.5–4.7 in) in diameter. Leaves are 1–1.3 m (39–51 in) long, and 1–1.4 m (3.3–4.6 ft) in diameter. Spathe is 30–55 cm (12–21.5 in) long. Flowers are white on the outside, to a purple-black color in the inside. Seeds are 9 mm (0.35 in) long, and 7 mm (0.28 in) wide.
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Pseudohydrosme gabunensis is being over-exploited as an ornamental plant, from which collectors are trying to make a profit on the illegal plant trade, or keeping the specimens for themselves, being very similar to Pseudohydrosme ebo.
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Conservation: Pseudohydrosme gabunensis is possibly extinct at some of its historical locations and is threatened at all of those which remain. At the type location, Sibang, formerly far outside Libreville, at least four gatherings have been made in what is now a small and highly visited forest patch inside Libreville (see notes under P. buettneri above). Measured on Google Earth, the forest is approximately a square, c. 470 m N to S and 420 m W to E, or about 0.25 km 2 (grid reference: 0 Ǫ 25 ′ 56.05 ″ N, 9 Ǫ 29 ′ 23.64 ″ E, 49 m alt.). It is now completely surrounded by the dense urban settlement of Libreville which has expanded greatly in the last 60 years. In 1960, at independence, the population of Libreville was 32,000. Since then it has expanded 20 - fold to, in 2013, 703,904 (https: // en. wikipedia. org / wiki / Libreville, accessed 19 September 2020) and has a vastly greater footprint. Sibang Arboretum, the surviving patch of forest of a once much greater area, is now known as one of the top two tourist destinations in Libreville. At the Cap Santa Clara location, the Forêt de la Mondah, known since 2012 as the Raponda Walker Arboretum (Walters et al., 2016), two collections were made, one in 1981 (see additional specimens). Since created as a protected area in 1934, it has been reduced in size, losing 40 % of its area in 80 years to habitat clearance and degradation due to its close proximity (c. 15 km) to the metropolis of Libreville which draws upon its trees for timber and firewood (Walters et al., 2016). It is not clear if either of the two specimens from St. Clara were from within the current protected area. The species has not been recorded from the Ogouué River since it was collected there by Leroy (1894 – 1895), despite intensive recent surveys in the lower reaches of the river whence it was probably collected. We have georeferenced the Leroy record on Lambarene since in Leroy’ s time this was a trading post on the lower reaches of the river and it is credible that he stopped and collected there, but this is uncertain. The historic site on the Komo River at Kango, whence it was collected by Chevalier (26828, P; fl. 2 Oct. 1912) is now on a major transnational route, and on Google Earth shows multiple cleared areas due to development. It is possible that it no longer survives at this location, especially since it has not been recorded here or anywhere near, in a century, despite the peak decades of botanical collection in Gabon having been at the end of the 20 th century (Sosef et al., 2005). Pseudohydrosme gabunensis was assessed as Endangered, EN B 2 ab (ii, iii) by Lovell & Cheek (2020) since it is or was known from ten specimens at five locations globally, with an area of occupation estimated as 24 km 2 using the 4 km 2 cell sizes preferred by IUCN (2012) and the threats detailed above. Threats in the Libreville area have already resulted in the possible global extinction of nine species, including Pseudohydrosme buettneri (see under that species, above). The extent of occurrence is calculated as 4,150 km 2. If the identification of the Congolese specimen can be completely confirmed as this species, and the site of its collection discovered, the area of occupation will likely be increased to 28 km 2 and the extent of occurrence also increased.
Floral visitors: Bogner (1981) collected as inferred pollinators two different flies identified as Diptera: Choridae, Sphaeroceridae, and two different beetles identified as Coleoptera: Scaphidiidae, Staphylinidae in association with Bogner 664. Reproductive biology: Hetterscheid & Bogner (2013: 106) working with cultivated plants, report that the female flowering phase is indicated by a faint yet clear lettuce-like scent as the spathe opens, at which time, for 2 days, the receptive stigmas are wet and sticky. After this time the stigmas turn darker brown, desiccate and are no longer receptive. Individuals are obligate outcrossers. Fruits take up 10 months to mature (Hetterscheid & Bogner, 2013). Germination and development: Germination takes 3 weeks to 10 months, producing a single small sagittate, entire leaf from a small rhizome. For several months to two years, new leaves are produced consecutively, usually each larger than its predecessor (Hetterscheid & Bogner, 2013). From the second leaf onwards slits may develop in the blade, and within two years the successively produced blades first becomes divided and finally develop the mature dracontoid pattern (see description). First flowering has occurred in as little as five years from first sowing (Hetterscheid & Bogner, 2013). In the wild, the time to maturity is likely to take longer due to predation, competition, and likely lower availability of nutrients
Pseudohydrosme gabun-ensis was found growing in the humus layer of a sandy loam in deep shade
Weitere
Global, Gabun
Distribution and ecology: Gabon, Estuaire, Moyen-Ogooué (probably) and Woleu-Ntem Provinces, known from five sites in lowland rainforest sometimes with Aucoumea gabonensis (Burseraceae); 0 – 100 m alt. Possibly also in Congo (location unknown, see notes below).
Gabon, Mundagebiet, Sibange-Farm, Wald am Maveilufer