Solanum corymbosum Jacq., Collectanea [Jacquin] 1: 78. 1787.
publication ID |
https://dx.doi.org/10.3897/phytokeys.231.100894 |
DOI |
https://doi.org/10.5281/zenodo.8360642 |
persistent identifier |
https://treatment.plazi.org/id/E42C3768-AD06-3E25-13E1-94516646E497 |
treatment provided by |
PhytoKeys by Pensoft (2023-08-30 08:21:26, last updated 2024-11-26 00:48:15) |
scientific name |
Solanum corymbosum Jacq., Collectanea [Jacquin] 1: 78. 1787. |
status |
|
13. Solanum corymbosum Jacq., Collectanea [Jacquin] 1: 78. 1787. View in CoL View at ENA
Figs 4B View Figure 4 , 41 View Figure 41 , 42 View Figure 42
Solanum corymbiferum J.F.Gmel., Syst. Nat., ed. 13[bis] 2(1): 384. 1791, nom. superfl. illeg. Type. Based on Solanum corymbosum Jacq. (cited in synonymy).
Solanum parviflorum Nocca, Ann. Bot. (Usteri) 6: 61.1793, nom. superfl. illeg. Type: Based on Solanum corymbosum Jacq. (cited in synonymy).
Solanum parviflorum Salisb., Prodr.Stirp. Chap. Allerton 134. 1796, nom. superfl. illeg. Type. Based on Solanum corymbosum Jacq. (cited in synonymy).
Solanum cymosum Ruiz & Pav., Fl. Peruv. [Ruiz & Pavon] 2: 31, t. 160. 1799. Type. Peru. "Habitat in Peruviae cultis, versuris et subhumidis locis per Limae et Chancay Provincias", H. Ruiz & J.A. Pavón s.n. (lectotype, designated by Knapp 2008b, pg. 312: MA [MA-747100]).
Solanum corymbosum Jacq. var. cymosum (Ruiz & Pav.) Pers., Syn. Pl. (Persoon) 1: 223. 1805. Type. Based on Solanum cymosum Ruiz & Pav.
Solanum leptanthum Dunal var. parvifolium Dunal, Solan. Syn. 9. 1816. Type. Peru. Cajamarca: sin. loc., F.W.H.A. von Humboldt & A. Bonpland s.n. (lectotype, designated by Knapp et al. 2019, pg. 50: P [P00670610]; isolectotypes: P [P00136337, P00136338]).
Solanum azureum Van Geert, Cat. Gén. 1879-1880 [Van Geert]: Solanum azureum . 1879. Type. Cultivated in the nursery of Auguste Van Geert in Gand, Belgium, from seeds sent by Mr. Roezl from Peru (no specimens cited; no original material found).
Type.
Cultivated in Vienna ["Hort. Bot. Vindob."] seeds said to be from Peru, N. von Jacquin s.n. (lectotype, designated by D’Arcy 1970, pg. 559: W [acc. # 0022473]) .
Description.
Annual to short-lived perennial subwoody herbs to 0.5 m high, branching at base. Stems terete, green to straw colour, sprawling, somewhat weak and decumbent, not markedly hollow; new growth nearly glabrous to sparsely pubescent with weak simple, uniseriate appressed 1-8-celled eglandular trichomes, these ca. 0.3 mm long; older stems glabrescent. Sympodial units difoliate or occasionally trifoliate, the leaves not geminate. Leaves simple, the blades 4.5-8 cm long, 1.5-4 cm wide, ovate-lanceolate, widest in the lower third, chartaceous to subcoriaceous, concolorous; both surfaces glabrous or sometimes sparsely ciliate near the base of the winged petiole; major veins 7-9 pairs, not clearly evident abaxially in live plants, paler in herbarium specimens; base long-attenuate, decurrent on the petiole; margins entire (in Peru rarely slightly 3-lobed, Croat 58409); apex acute; petioles 0.5-1 cm, glabrous to sparsely puberulent, winged to the base. Inflorescences internodal or opposite the leaves, 4-7 times branched, 2-3 cm long, with 20-50(-60) flowers spaced along the axis, nearly glabrous to sparsely pubescent; peduncle 0.1-2 cm, straight in fruit; pedicels 2-2.5 mm long, less than 0.5 mm in diameter at the base, ca. 0.5 mm in diameter at the apex, spreading, articulated at the base; pedicel scars spaced 1-3 mm apart. Buds globose, the corolla about halfway exserted from the calyx tube before anthesis, the tips of the corolla lobes often much more pubescent than the calyx. Flowers 5-merous, cosexual (hermaphroditic). Calyx tube 0.5-1 mm long, conical or broadly conical, the lobes 0.5-0.6 mm long, ca. 0.5 mm wide, broadly triangular, glabrous to very sparsely puberulent with simple, uniseriate trichomes. Corolla 0.5-1 cm in diameter, white or purple, the abaxial surface usually purple, rotate-stellate, the lobes 1-2.5 mm long, 1-1.5 mm wide, broadly triangular, reflexed at anthesis, later spreading, glabrous adaxially, minutely white-puberulent abaxially on the tips. Stamens equal; filament tube minute; free portion of the filaments ca. 0.2 mm long, adaxially pubescent with simple tangled white trichomes; anthers 0.8-1.5(-1.8) mm long, ca. 0.5 mm wide, ellipsoid, yellow, somewhat connivent, poricidal at the tips, the pores lengthening to slits with age. Ovary globose, glabrous; style ca. 2 mm long, straight, hardly exserted beyond the anther cone, pubescent in the lower 2/3 with tangled, white uniseriate simple weak-walled trichomes; stigma globose-capitate, minutely papillate, pale green in live plants. Fruit a globose berry, 0.4-0.6 cm in diameter, orange to red when ripe, opaque, the pericarp shiny or matte, translucent, glabrous; fruiting pedicels 0.2-0.3 cm long, ca. 0.5 mm in diameter at base, ca. 0.6 mm in diameter at the apex, strongly recurved at the very base, not persistent; fruiting calyx scarcely accrescent, the tube ca. 1 mm long, the lobes 1-1.3 mm long, appressed to the berry. Seeds 20-30 per berry, 1.5-1.8 mm long, 1.2-1.4 mm wide, flattened reniform with a central hilum, light yellow-tan or reddish brown in herbarium material, the surfaces minutely pitted, the testal cells with sinuate margins. Stone cells 2, ca. 1.5 mm in diameter, globose, prominent near the apex of the berry. Chromosome number: 2n = 24 ( Chiarini et al. 2017, voucher Särkinen et al. 4075).
Distribution
(Fig. 43 View Figure 43 ). Solanum corymbosum occurs on the western slopes of the Andes in Peru (Depts. Amazonas, Ancash, Cajamarca, Huánuco, Lambayeque, La Libertad, Lima, Moquegua), and is naturalised in central and southern Mexico, possibly through introduction in colonial times (see discussion in Knapp et al. 2019).
Ecology and habitat.
Solanum corymbosum grows in open, disturbed areas in landslides and along roads from sea level [in coastal lomas vegetation] to 2,900 m elevation.
Common names and uses.
Peru. Ancash: cchapchinya ( Gómez 51); Cusco: ñuñuma, qusmayllu ( Roersch 1994, as S. radicans ); Huánuco: puslita mullaca ( Cárdenas 12275); La Libertad: hierba mora (Leiva et al. 707); Lima: hierba mora (Ferreyra 716, Ridoutt 11183a); Puno: chetenguya ( Roersch 1994, as. S. radicans ). Roersch (1994) records use of leaves in a tea as treatment for sore throats and tonsillitis, macerated leaves as a plaster for swellings, and as a wash for colicky babies and for rheumatism (in combination with other medicinal plants). Although Roersch reports this plant as S. radicans , the illustration ( Roersch 1994: 633) and description are clearly S. corymbosum .
Preliminary conservation status
( IUCN 2022). Least Concern [LC]. EOO = 338,062 km2 [LC]; AOO = 240 km2 [EN]; calculated using South American distribution only. Solanum corymbosum has a disjunct distribution in Peru and Mexico; in its native range in Peru the species is quite widely distributed, but in Mexico potential morphological differences from Peruvian populations suggests it could be of conservation concern in its introduced range ( Knapp et al. 2019). In Peru it occurs in several protected areas (e.g., Reserva Nacional Calipuy and the lower elevations of Parque Nacional Huascarán).
Discussion.
Solanum corymbosum is a member of the Radicans group ( Särkinen et al. 2015b) and has an unusual disjunct distribution in Peru and Mexico; Mexican populations are thought to represent an introduction of this species in post-Columbian times ( Knapp et al. 2019). Populations in Mexico show nearly identical haplotypes to those from the coastal regions in Peru ( Mitchell 2014), supporting this hypothesis.
Solanum corymbosum can be distinguished from other members of the Radicans group in its simple, entire leaves, small orange to red fruits with two large apical stone cells, its highly branched inflorescences and diminutive flowers with rotate-stellate corollas that are usually white adaxially and purple abaxially. Other members of the group have 3- to 5-lobed leaves (e.g., S. palitans , S. radicans , S. tripartitum ), although a population of S. tripartitum from the Province of Salta, Argentina appears to be uniformly simple-leaved. Corolla size of S. corymbosum overlaps with these plants at its upper range, but flowers of S. corymbosum are generally smaller (0.5-1 cm in diameter) than those of S. tripartitum (0.9-1.1 cm in diameter), and S. tripartitum has more than two stone cells per berry. The two species are not sympatric.
Chiarini, FE, Lipari, D, Barboza, GE, Knapp, S, 2017. Solanaceae. In: Marhold, K, Bresitwiser, I, Eds., IAPT/IOPB chromosome data 25. Taxon 66(5): 1246 - 1247, DOI: https://doi.org/10.12705/665.29
D'Arcy, WG, 1970. Jacquin names, some notes on their typification. Taxon 19 (4): 554 - 560, DOI: https://doi.org/10.2307/1218948
2022. . https://www.iucnredlist.org/resources/redlistguidelines
Knapp, S, 2008b. Lectotypification of Ruiz and Pavon's names in Solanum (Solanaceae). Anales del Jardin Botanico de Madrid 65 (2): 307 - 329, DOI: https://doi.org/10.3989/ajbm.2008.v65.i2.295
Knapp, S, Barboza, GE, Bohs, L, Saerkinen, T, 2019. A revision of the Morelloid Clade of Solanum L. (Solanaceae) in the Caribbean and North and Central America. PhytoKeys 123: 1 - 174, DOI: https://doi.org/10.3897/phytokeys.123.31738
Mitchell, LJM, 2014. The role of geography versus ecology in species diversification in the tropical Andes: case study of Solanum section Parasolanum. MSc dissertation, University of Edinburgh and Royal Botanic Garden, Edinburgh.
Roersch, C, 1994. Plantas Medicinales en el Sur Andino del Peru. 2 vols. Koeltz Scientific Books, Koenigstein.
Saerkinen, T, Barboza, GE, Knapp, S, 2015b. True Black nightshades: Phylogeny and delimitation of the Morelloid clade of Solanum. Taxon 64 (5): 945 - 958, DOI: https://doi.org/10.12705/645.5
Figure 4. Representative fruits, seeds and stone cells of South American morelloids A bilobed fruits in S. tripartitum with fully mature red berries at the base of the inflorescence and maturing green, yellow, and orange fruits more distally B orange-red fleshy berries of S. corymbosum in highly branched inflorescences C fully mature marbled fruits in S. physalifolium D immature ellipsoid fruits of S. antisuyo E fully mature fruits of S. antisuyo F immature green fruits amongst fully mature purple-black fruits in S. cochabambense G fully mature fruits of S. polytrichostylum H stone cells (also known as sclerotic granules or brachysclerids) found in the fruits of most species of the Morelloid clade (left side of photo) next to the teardrop shaped seeds (right side of photo; S. umalilaense Manoko) I stone cells visible in dried fruits of herbarium specimens (S. triflorum). (A Barboza 3563 B Saerkinen et al. 4604 B C Knapp et al. 10334 D Gonzales 10256 E Gonzales 10256 F Knapp et al. 10363 G Saerkinen et al. 5277 H Nijmegen accession A 24750133 I Podlech 8624 BM 000848286). Photos by P. Gonzales, S. Knapp, and T. Saerkinen.
Figure 41. Solanum corymbosum A habit B detail of adaxial leaf surface C detail of abaxial leaf surface D flowering branch E floral bud F dissected flower G fruiting branch H maturing fruit (A-F van der Werff et al. 14657 G, H Ochoa 14625). Illustration by R. Wise. Previously published in Knapp et al. (2019: 52).
Figure 42. Solanum corymbosum A habit B inflorescence C flowers at full anthesis and buds D fully mature red-orange fruits with appressed calyx lobes (A Saerkinen et al. 4604 B B, D Saerkinen et al. 4078 D Saerkinen et al. 4509). Photos by T. Saerkinen. Previously published in Knapp et al. (2019: 53).
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.
Kingdom |
|
Phylum |
|
Class |
|
Order |
|
Family |
|
Genus |