Solanaceae Source

A global taxonomic resource for the nightshade family

Solanum hastifolium

Citation author: 
Hochst. ex Dunal
Citation: 
Prodr. [A.P. de Candolle] 13(1): 284. 1852.
Type: 
SUDAN. Mt. Cordofan, Arasch-Cool, Oct 1839, C. Kotschy 393 (lectotype designated by Vorontsova & Knapp 2012: P! [P00344017]; isolectotypes: BM! [BM000847414], GOET! [GOET003535], K [K000414008, K000414010], M! [M0105603, M0105604], P! [P00344018], W! [W0000607], WRSL).
Last edited by: 
Sandra Knapp (May 2014)
Written by: 
Maria S. Vorontsova & Sandra Knapp
Habit: 
Erect or scandent herb to shrub, 0.3-1(-1.5) m, prickly. Young stems terete, sparsely to densely stellate-pubescent and prickly, with porrect, sessile or variously stalked trichomes, the stalks to 0.1 mm long, the rays 5-8, 0.1-0.3 mm long, the midpoints reduced or same length as the rays, sometimes with minute simple hairs, the prickles 1-4 mm long, 0.5-3.5 mm wide at base, curved, sometimes almost straight, pale yellow to gray or brown, glabrous, spaced 3-10 mm apart; bark of older stems glabrous, gray to brown.
Sympodial structure: 
Sympodial units difoliate, not geminate.
Leaves: 
Leaves simple, the blades 2.5-6.5 cm long, 0.8-2.5 cm wide, 2-4 times longer than wide, ovate to lanceolate, chartaceous, drying concolorous, yellow-green, moderately to sparsely stellate-pubescent on both surfaces, with porrect, translucent, sessile or subsessile trichomes, the stalks to 0.1 mm long, the rays 4-8, 0.1-0.4 mm long, the midpoints reduced or same length as the rays, with 0-5 prickles on both surfaces; the primary veins 3-4(-5) pairs, the tertiary venation not visible to the naked eye; base obtuse to cuneate, sometimes truncate; margins lobed, the lobes 2-4 on each side, 0-1 cm long, extending to 2/3 of the distance to the midvein, broad-deltate, apically rounded; apex acute to obtuse; petiole 0.6-1.2 cm long, 1/3-1/4 of the leaf blade length, moderately to sparsely stellate-pubescent, unarmed.
Inflorescences: 
Inflorescences apparently terminal or lateral, 1-3 cm long, not branched, with 3-5 flowers, 1-3 flowers open at any one time, moderately to sparsely stellate-pubescent, unarmed; peduncle absent; pedicels 0.6-1.5 cm long, erect, articulated at the base, moderately to sparsely stellate-pubescent, unarmed; pedicel scars spaced 1-4 mm apart.
Flowers: 
Flowers 4-5-merous, apparently all perfect. Calyx 4-6 mm long, moderately to sparsely stellate-pubescent, unarmed, the lobes 2-4.5 mm long, deltate, apically acute to acuminate. Corolla 1.4-2 cm in diameter, pale mauve to purple, sometimes white, stellate, lobed for ca. 4/5 of the way to the base, the lobes 6-10 mm long, 1.8-2.5 mm wide, lanceolate to oblong, reflexed or spreading, moderately stellate-pubescent abaxially, the trichomes porrect, sessile, the rays 5-8, 0.1-0.25 mm long, the midpoints shorter than the rays. Stamens equal, with the filament tube 0.8-1.1 mm long, the free portion of the filaments 0.1-0.3 mm long; anthers 5-8 mm long, spreading, tapering, poricidal at the tips. Ovary densely stellate-pubescent in the upper 1/5; style 1-1.3 cm long, filiform, straight or curved towards the tip, stellate-pubescent for most of its length or only the lower 1/2.
Fruits: 
Fruit a spherical berry, 1-4 per infructescence, 0.6-0.8 cm in diameter, the pericarp smooth, dark green with pale green and cream markings when young, bright red at maturity, glabrous; fruiting pedicels 1.1-1.9 cm long, 0.3-0.4 mm in diameter at base, herbaceous, erect to pendulous, unarmed; fruiting calyx lobes not elongating, 1/4-2/3 the length of the mature fruit, reflexed, unarmed.
Seeds: 
Seeds ca. 10 per berry, 2.8-3.3 mm long, 2-2.8 mm wide, flattened-reniform, dull yellow to orange-brown.
Chromosome number: 

Not known

Distribution: 

Widespread, mainly inland eastern African species found from Sudan, Ethiopia and Somalia to Uganda and northern Tanzania; reported to occur as far west as Chad by Brundu & Camarda (2013, no specimens seen); collected in dry Acacia (Vachellia) scrub, open places, disturbed vegetation and roadsides on sand, clay, loam and black cotton soil, sea level – 1500 m elevation.

Phenology: 
Flowering and fruiting throughout the year.
Phylogeny: 

A member of the Old World clade within subgenus Leptostemonum (Levin et al., 2006). Solanum hastifolium was not included in the analyses of Vorontsova et al. (2013), but is probably close to Solanum glabratum and part ofthe Anguivi Grade. 

Commentary: 

Solanum hastifolium is a widespread polymorphic weedy species recognized by its lobed leaves, retrorse or recurved prickles, and inflorescences with more than 2 flowers. Sudanese collections more often mention S. hastifolium as a climbing plant, while we have only seen it growing as a shrub in Kenya. Ethiopian collections tend to have more entire leaves. The type collection is uncharacteristic of S. hastifolium; its leaves are more strongly hastate than typical, and its habit is more climbing. Friis et al. (2010) consider S. hastifolium endemic to the Somalia-Masai phytogeographical region but its distribution extends west into the Sudanian phytogeographical region (White 1983, Jaeger & Hepper 1986).

Solanum hastifolium is morphologically similar and apparently closely related to S. glabratum, S. setaceum, and S. taitense. Solanum taitense and S. setaceum occur within the distribution of S. hastifolium. Both are locally common and uniform species that are morphologically similar to some forms of S. hastifolium. Solanum setaceum is easy to distinguish by the filiform bristles on its young stems. Solanum taitense is more difficult to distinguish reliably, as no single character separates all the specimens, but S. hastifolium has the majority of the following: lobed leaves 2.6-6.5 cm long (versus entire to subentire leaves 1.2-3(3.5) cm long in S. taitense), abundant prickles 1-4 mm long, spaced 3-10 mm apart (versus inconspicuous more closely spaced prickles up to 1(2) mm long in S. taitense), more than 3 flowers per inflorescence (versus 1-2(3) flowers per inflorescence in S. taitense), corolla 1.4-2 cm in diameter (versus corolla 1-1.7 cm in diameter in S. taitense), anthers 5-8 mm long (versus anthers 4-6 mm long in S. taitense), plant sparsely to moderately pubescent (versus S. taitense densely pubescent), and trichomes sessile to short-stalked (versus stalked trichomes on all vegetative surfaces with inflated trichome stalks on the adaxial side of the leaves in S. taitense).

Solanum hastifolium is a more southerly species than S. glabratum, and where the two overlap in Ethiopia and Somalia rare collections with intermediate morphological charaters have been made.  Consistent differences between the two species include the following: S. hastifolium often has a scandent or climbing habit (versus S. glabratum always erect), fewer gray or brown recurved or hooked prickles 1-4 mm long and 0.5-3.5 mm wide (versus hooked flattened yellow prickles 2-5 mm long and 1.5-5 mm wide in S. glabratum), red fruit (versus orange or red fruit in S. glabratum), more indumentum with larger trichomes that are often stalked (versus fewer small sessile trichomes in S. glabratum), and occupies wetter environments at lower elevations. The best distinguishing character for identification purposes is the presence of a petiole in S. hastifolium (versus leaf blade decurrent at the base and a lack of a clear petiole in S. glabratum).

Jaeger (1985) suggested that S. hastifolium may be conspecific with the Indian S. trilobatum L. The two species are clearly distinct, however, and S. hastifolium can be distinguished from S. trilobatum by its more deeply stellate corolla (versus more shallowly lobed corolla in S. trilobatum), larger leaf length to width ratio (versus wider leaves in S. trilobatum), and yellow-green drying color (versus red-brown drying color in S. trilobatum).

In describing S. cynanchoides, Chiovenda (1932) did not cite a herbarium in which the type specimen was held. We have selected that in FT as the lectotype; the illustration in Chiovenda (1932) is clearly of that sheet, and that herbarium received much if not most of the material from the Italian colonial collections (although some is still held in PAL).

References: 

Brundu, G., Camarda, I. 2013. The Flora of Chad: a checklist and brief analysis. PhytoKeys 23: 1-18. doi: 10.3897/phytokeys.23.4752

Chiovenda, E. 1932. Solanaceae. In Flora Somala, Volume 2, pp. 331-336. Rome: published by the author.

Friis, I., Sebsebe Demissew, and P. van Breugel. 2010. Atlas of the potential vegetation of Ethiopia. Biol. Skr. Dan. Vid. Selsk. 58: 1-307.

Jaeger, P.-M.L. 1985. Systematic studies in the genus Solanum in Africa. PhD thesis, University of Birmingham, United Kingdom.

Jaeger, P.-M.L. & F.N. Hepper 1986. A review of the genus Solanum in Africa. In: W.G. D’Arcy (ed.), Solanaceae. Biology and Systematics. Proceedings of the Second International Symposium on the Biology and Systematics of the Solanaceae, pp. 41-55. Columbia University Press, New York, USA.

Levin, R.A., N.R. Myers, & L. Bohs 2006. Phylogenetic relationships among the "spiny" solanums (Solanum subgenus Leptostemonum). Amer. J. Bot. 93: 157-169.

Vorontsova, M. S., S. Stern, L. Bohs, and S. Knapp. 2013. African spiny Solanum (subgenus Leptostemonum, Solanaceae): a thorny phylogenetic tangle. Bot. J. Linn. Soc. 173: 176-193. doi:10.1111/boj.12053

White, F. 1983. The vegetation of Africa: a descriptive memoir to accompany the UNESCO/AETFAT/UNSO vegetation map of Africa. UNESCO, Paris, France.

Common names and uses: 

Local Names. Kenya: Ethsakilele (Turkana language, Adamson 47), Gala-out (Samburu language, Adamson 47). Uganda: Edonamuroi (Dyson-Hudson 216).

Uses. Medicinal.

Wed, 2013-11-20 10:59 -- sandy
Scratchpads developed and conceived by (alphabetical): Ed Baker, Katherine Bouton Alice Heaton Dimitris Koureas, Laurence Livermore, Dave Roberts, Simon Rycroft, Ben Scott, Vince Smith