Weinmannia stenostachya Baker
publication ID |
https://doi.org/ 10.5281/zenodo.5180157 |
persistent identifier |
https://treatment.plazi.org/id/0D3E87DC-FFE0-FFFE-F7D2-F9BF4BB1CE01 |
treatment provided by |
Carolina |
scientific name |
Weinmannia stenostachya Baker |
status |
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Weinmannia stenostachya Baker View in CoL (species-group G)
Kew Bull. 1895: 103 (1895). — Type: Baron 6406, northern Madagascar (holo-, K!; iso-, P!) .
COLLECTIONS EXAMINED FROM MAROJEJY. — wide, elliptic to obovate, decurrent at the base for MADAGASCAR, Prov. Antsiranana: Deroin & Badré 74, 3- 7 mm, apex obtuse, margin serrulate throughrive gauche de la m Manantenina ,, versant sud du out, Beondroka, 1130 14°26’S, 49°48’E ( MO, P); teeth blunt, sinus shallow, with a small dark Miller & Randrianasolo 4456, western slopes and sum- gland, lateral veins 15-22 per leaflet, semicraspemit of Mt. Beondroka , 830-1210 m ( MO, P, TAN). dodromous, veins terminating at the sinus GoogleMaps .
Flower-bearing axes spicate, spikes 4.5-7 cm
long, axis puberulous, usually borne in pairs from
This species is widespread in the northern, a short peduncle, 0.7-1.5 mm long, with a vegeeastern and southern uplands. See discussion tative bud between each spike (i.e. forming under W. arguta about the distinguishing features dyads), dyads borne axillary and sometimes terof W. stenostachya . minally near the distal end of stems, or spikes
occasionally borne from leaf axils along the main
stem. Floral bracts curled, ligulate, c. 1 mm long,
Weinmannia venosa J.C. Bradford , sp. nov. subtending solitary flowers that spread apically in (species-group G) a line, flowers inserted up to 3 mm from their
bract.
Frutex vel arbor 2-12 m alta. Folia plerumque 3-foli- Flowers bisexual or female?, pentamerous, olata, glabra, rhachidi non alata, foliolis lateralibus ellip- diplostemonous, sepal lobes triangular, 1- ticis, 1-4.5 cm longis, 0.8-2 cm latis, apiceum obtusis, basim acutis, margine serrulata. Inflorescentia spicata, 1.25 mm long, sparsely puberulous, petals 4.5-7 cm longa, bracteis c. 1 mm longis, subtendens green?, elliptic, 1.2-1.4 mm long, 1 mm wide, florem sessilis, singularis. Ovarium puberulum . Semina sparsely puberulous, stamens 10, filaments 2.5- comose. 3 mm long (1 mm, female flower?), floral nectary
thin, c. 0.5 mm tall, ovary ovoid, 1 mm tall,
TYPUS,. — Rakotomalaza Prov. , Ravelonarivo & Messmer densely puberulous, ovules numerous, c. 16 per
959 Madagascar. Antsiranana, Réserve Naturelle Intégrale de Marojejy , versant ouest et sud- locule, styles 1.8-2 mm long. Capsules 4-5 mm ouest du sommet de Marojejy, ouest et sud du campe- long, calyx persistent, endocarp and exocarp sepment 5, 1875 m, 14°27’S, 49°44’E, 18-19 Nov. 1996 arating in old fruits, seeds elliptic to slightly reni- (holo-, MO; iso-, TAN). form, 1.25 mm long, 0.6-0.7 mm wide, comose GoogleMaps ,
trichomes c. 0.5-1 mm long. — Fig. 6 View Fig .
Tree or shrub, 2-12 m tall, branching every 1- few nodes, occassionally dichotomously, intern- PARATYPES. — MADAGASCAR, Prov. Antsiranana: odes 0.7-5.5 cm long, lateral branches with short Bradford & Rafamantanantsoa 719, 722, near source of
Andranomifototra river, NE of summit of Marojejy,
internodes, c. 1-2 mm long, then internodes of near “Camp 4” and forested slopes north of the camp, c. 1 cm or longer, the stems gray, cylindric, the 1520-1600 m, 14°26’24”S, 49°44’30”E ( MO, P, young growth with dense, orange pubescence. TAN); Humbert, Capuron & Cours 24726, massif de Axillary buds stipulate, stipules c. 2 mm long, l’Anjanaharibe (pentes et sommet nord) à l’ouest 2.5 mm wide, unfused, pubescent, caducous; d’Andapa (haute Andramonta, bassin de la Lokoho: GoogleMaps
nord-est), 1600-1800 m (MO, P).— Prov. Toliara:
medial stipules caducous, inner surface glabrous, Rakotomalaza 517, Fort-Dauphin, Eminiminy, RNI outer surface pubescent, elliptic to ovate, 4-7 mm #11 Andohahela, parcelle #1, campement 4, sur la long, colletors 0.3-0.7 mm long, red-black. crête, 1500-1650 m, 24°34’S, 46°44’E (MO, P). Leaves decussate, imparipinnate, (1-)3-5(-7)-foliolate, 2.5-8.5 cm long, petiole 0.3-1.5 cm long, Weinmannia venosa is known from two disrachis not winged, both lamina surfaces glabrous junct populations at Marojejy and Andohahela in mature leaves except for pubescent midribs, more than 1500 km apart, and possibly from a young leaves sparsely pubescent on abaxial lam- third population at Andringitra (Guillaumet ina; lateral leaflets elliptic, 1-4.5 cm long, 0.8- 3388). 2 cm wide, the apex obtuse, the base concave The leaves of W. venosa resemble those of distally, convex basally, terminal leaflets slightly W. hildebrandtii ; both have prominent venation, larger than the laterals, 1.6-6 cm long, 1.3-3 cm but they differ most obviously by the number of
flowers subtended by a bract (one in W. venosa versus c. four in W. hildebrandtii ). With its spicate inflorescence, pubescent ovaries and comose seeds, W. venosa is similar to W. humblottii , W. sanguisugarum and W. arguta . However, Weinmannia venosa has fewer leaflets (usually 3) than W. sanguisugarum (c. 15). W. venosa has elliptic to obtuse leaflets that are apically obtuse, whereas leafets of W. arguta are elliptic to ovate and apically acute. In W. venosa , the leaves are generally larger than in W. humblotii , and the venation in W. venosa is more prominent than in W. humblottii . Weinmannia venosa does not have a slightly laminar rachis, which is a common feature in W. humblottii .
Bradford 722 appears to have diminuitive male organs, whereas Rakotomalaza 959 from the same population has bisexual flowers. Wart-like bumps on the leaves of Bradford 722 suggest that the plant is diseased, which may have affected floral development. Unisexual flowers are not known in Malagasy species of Weinmannia , but do occur elsewhere in the genus.
K |
Royal Botanic Gardens |
P |
Museum National d' Histoire Naturelle, Paris (MNHN) - Vascular Plants |
MO |
Missouri Botanical Garden |
TAN |
Parc de Tsimbazaza |
No known copyright restrictions apply. See Agosti, D., Egloff, W., 2009. Taxonomic information exchange and copyright: the Plazi approach. BMC Research Notes 2009, 2:53 for further explanation.
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