Teramnus labialis
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Teramnus labialis
Teramnus labialis (L. f.) Spreng.
Subordinate taxa:
Teramnus labialis (L. f.) Spreng. subsp. arabicus Verdc.
Teramnus labialis (L. f.) Spreng. subsp. labialis var. abyssinicus (Hochst. ex A. Rich.) Verdc.
Teramnus labialis (L. f.) Spreng. subsp. labialis var. labialis
Family: Fabaceae (alt. Leguminosae) subfamily: Faboideae tribe: Phaseoleae subtribe: Glycininae.
Extremely variable perennial, twining or prostrate, trailing, some forms stoloniferous, sometimes woody at the base. Stems 0.3‒4.0 m long, angular, slender, often covered with adpressed to spreading white to ferruginous hairs, sometimes glabrescent. Leaflets rounded, elliptic, ovate, obovate, narrowly oblong or lanceolate, (1‒) 3‒6 (‒8) cm long, (0.5‒) 2‒3.5 (‒5) cm wide, emarginate to acuminate at the apex, mostly rounded at the base, glabrous to densely covered with white or ferruginous hairs on both surfaces; petioles 0.9‒4 cm long; rachis 1‒9 mm long; petiolules ( 2 mm long; stipules narrowly lanceolate, 2‒3 mm long. Inflorescence a slender axillary raceme, with few to many flowers along the 0.3‒10 (‒15) cm long rachis; peduncle 0.8‒3 cm long. Calyx tube glabrescent or hairy, ribbed, 1‒3 mm long, lobes lanceolate, 0.8‒3 mm long, acute, usually densely hairy; standard white, cream, pink, pale salmon, mauve or magenta, sometimes with deeper coloured splash, obovate, 5 mm long, 3.5 mm wide. Pods linear or slightly falcate, 2.5‒6 cm long, 2‒4 mm wide, glabrescent to densely covered with adpressed or spreading hairs; upturned stylar beak 2‒3 mm long; 7‒12 seeds/pod. Seeds yellow-brown to dark purplish-brown, oblong or almost cylindrical, smooth or covered with a granular encrustation, 2‒3 mm long, 1.2‒2 mm across; hilum minute, aril slightly developed, white with a small scale-like extension. 110,000‒370,000 seeds per kg.
subsp. labialis var. abyssinicus: seeds smooth; leaflets often smaller; upper surface of leaflets glabrous.
subsp. labialis var. labialis: seeds smooth; leaflets often smaller; upper surface of leaflets hairy.
subsp. arabicus: seeds with granular surface; leaflets elliptic up to 7.5 cm long; pods usually with appressed hairs, but if spreading then leaflets longer and narrower.
Teramnus: distinctly upward-curved beak on the pod
Glycine and Neonotonia: pod acuminate to weakly uncinate
Africa: adagbudu (Yoruba, Nigeria)
Asia: 软荚豆 ruan jia dou (China); cantingan, kakacangan sapi, kacang sapi, koselan, ron kaka (Java); kacang tikus (the Moluccas); mangkit-bagin (Tagalog, Philippines), balagun (Cebuano, Philippines), bagon-bagon (Samal, Philippines); voë romiet (Cambodia); mon sran gre-u-i-dab ma, mon sran gro-u-i-dab ma (Tibet)
English: blue wiss (USA); rabbit vine, horse vine (Barbados); green gram, Vogel-tephrosis (India)
Indian Ocean: pistache marronne (Madagascar, Réunion); teloravina, vahilandy (Madagascar); uviji matra, uvigi mtoumama, muvunge muche, mjividza, famaki angotu (Bushi, Mayotte)
Latin America: curvicán de jutía, teramnus, tripa de jutía (Cuba); frijolillo (Puerto Rico, Virgin Islands)
South Asia: mashani (Bengali); कल्याण kalyan, लोमशपर्णिनी lomashparnini, मशानी mashani, माषपर्णी mashaparni, पाण्डुलोमा pandu-loma, masban, mashoni, van(a) udad (Hindi); ಅಡವಿ ಉದ್ದು adavi uddu, mooshaparni, moosha parna (Kannada); रानउडीद ran-udid (Konkani); cherukattuzhunnu, kattualandu, kattulunnu (Malayalam); रानउडीद ran-udid, kudu-udid, ran-udida (Marathi); ban-kultha (Oriya); हयःपुच्छी hayahapuchchi, कल्याणी kalyani, माषपर्णी mashaparni, विसारिणी visarini (Sanskrit); වල් කොල්ලු wal-kollu (Sinhala, Sri Lanka);மாஷபருணி mashaparuni (Tamil); కారు మీనుముల్లు karu minumullu, adavi mahasaha (Telugu); kattuzhunninveru
Native:
Africa: Angola; Benin; Burundi; Cameroon; Central African Republic; Chad (south); Côte d'Ivoire; Democratic Republic of the Congo; Ethiopia; Ghana; Guinea-Bissau; Kenya; Liberia; Mali; Mozambique; Nigeria (s.); Rwanda; São Tomé & Príncipe; Senegal; Sierra Leone; Somalia; South Africa; Sudan; Swaziland; Tanzania; Togo; Uganda; Zambia; Zimbabwe
Western Indian Ocean: Comoros; Madagascar; Mauritius; Réunion; Seychelles
Asia: Bangladesh; Cambodia; India; Indonesia; Laos; Malaysia; Myanmar; Philippines; Saudi Arabia; Sri Lanka; Taiwan (s.); Thailand; Vietnam; Yemen
Pacific: Guam; Papua New Guinea
Caribbean: Antigua and Barbuda; Barbados; British Virgin Is; Cuba; Grenada; Guadeloupe; Haiti; Hispaniola; Jamaica; Martinique; Montserrat; Puerto Rico; St. Lucia; St. Vincent and The Grenadines.
Central America: Guatemala; Nicaragua; Panama
South America: Guyana
Cultivated:
Caribbean: Cuba
Component of permanent pastures, with potential for agroforestry applications due to moderate shade tolerance. It can be grazed fairly intensively or cut for green chop. It is used commercially as a forage in Cuba, but does not appear to be sown elsewhere for this purpose.
Has grown well as a ground cover and soil improver under citrus (Citrus sinensis), banana (Musa sp.) and coconut (Cocos nucifera).
Tribal people use seeds as food, and various parts of the plant are used in natural medicines in India. It is well-recognized as a medicinal plant for its antiinflammatory activity in the Ayurvedic system of medicine, and has been reported to be useful in treating rheumatism, tuberculosis, nerve disorders, paralysis and catarrh.
Found in well- (rarely poorly-) drained sands to clays with pH (5.5‒) 6.0‒8.0 (‒9.0). Although originating from mostly near neutral to alkaline soils, some ecotypes have performed well on soils with pH 5.0‒5.5. 'Semilla Clara' is not as well adapted to acid soils as other warm-season species such as Macroptilium atropurpureum (Siratro) and Stylosanthes guianensis. While a few accessions have been collected in sodic areas, T. labialis is generally considered to have low salt tolerance.
Mostly collected in run-on or moister areas, in regions with average annual rainfall (500‒) 750‒1,500 (‒2,500) mm. Probably best sown in areas with rainfall >1,000 mm. In some areas, it grows with sour-grass (Paspalum conjugatum), a species common in shaded situations, often on acid, poorly drained soils. At least some ecotypes shed their leaves during dry periods and are killed off by the prolonged dry periods.
Occurs between about 25º N and 29º S, and from sea level to 3,000 m asl, representing a range in average annual temperatures of about 14‒27 ºC, sometimes with frost. There is some variation in frost tolerance within the species, although all accessions that have been tested have shown some measure of susceptibility. Most have the tops killed by light to moderate frost, but recover with the onset of warmer conditions.
Has grown well under citrus (Citrus sinensis), banana (Musa sp.) and coconut (Cocos nucifera). Exhibits shade tolerance greater than that of Vigna hosei, but less than that of the very shade tolerant Grona heterophylla and Arachis pintoi .
The majority appear to flower in response to shortening daylength. Flowering time varies markedly among provenances, some flowering in about 70 days from a spring planting and others 200 days.
Tolerance of defoliation varies according to growth habit, lower growing, stoloniferous varieties normally being more tolerant than more upright types.
No information available, but not normally grown in fire-prone situations.
Guidelines for establishment and management of sown forages.
Generally, seed does not require scarification. However, levels of hard seed can be high in some samples, and scarification may be necessary to achieve at least 50% germination. Although T. labialis appears somewhat promiscuous in relation to rhizobial requirements, inoculation with CB 756 (Australia) or an equivalent strain may be beneficial. Seed can be broadcast or sown at 2‒3 kg/ha in rows 50‒75 cm apart, and no more than 3 cm deep. Seed is small and seedling development relatively slow, so seed should be sown into a well-prepared seedbed, with the area rolled after sowing. Stands take 6‒8 months to become established.
T. labialis requires moderately fertile soil. Application of 20 kg/ha P and 40 kg/ha K is recommended on deficient soils. In view of the high demand for Mo by the closely related Neonotonia wightii, and in the absence of information specific to T. labialis, it may be advisable to apply 100‒200 g/ha Mo every 3 years on more acid soils.
T. labialis grows well in mixed pastures, persisting and producing considerable bulk without smothering the grasses. It is probably not sufficiently aggressive to combine with more competitive grasses such as Paspalum notatum, nor does it twine to a sufficient height to combine with unmanaged tall grasses such as Megathyrsus maximus. However, it can combine with these larger species if they are maintained at about 50‒80 cm high.
Grasses: Axonopus fissifolius, Bothriochloa pertusa, Dichanthium aristatum, Digitaria eriantha (not pangola), Stenotaphrum secundatum.
Legumes: Macroptilium atropurpureum, Neonotonia wightii, Vigna parkeri.
It is not affected by pests and diseases to any great extent, although leaf damage caused by Fusarium and Alternaria has been recorded, particularly in the wet season. It is less affected by Alternaria than are Macroptilium atropurpureum and Neonotonia wightii . Some leaf damage has also been caused by the banded cucumber beetle, Diabrotica balteata (Coleoptera: Chrysomelidae).
T. labialis has become naturalized outside its native range.
There is no evidence of its being considered a serious weed in any of the areas to which it has been introduced. It is often found in disturbed situations.
Maintains a high leaf to stem ratio, with crude protein levels of leaf and stem being measured at 21 and 10% respectively, compared with 18 and 11% in Neonotonia wightii. At the same time, Ca levels in leaf and stem of T. labialis were 1.2 and 1%, and P levels 0.3 and 0.2%.
Cattle select T. labialis in preference to N. wightii. Although it is well eaten by cattle, one report suggests less so by sheep.
No record of toxicity.
T. labialis types range from low-growing, soft herbs to vigorous plants that can twine to over 1 m high. While more productive types can produce 10‒16 t/ha DM, many produce much lower annual yields.
No data available.
2n = 20, 24, 28. There appears to be no variation within accessions grown from nursery-produced seed, suggesting this is a closely selfed species.
Pod-set often occurs beneath the foliar canopy, and close to ground level, making mechanical harvesting difficult. In 'Semilla Clara', which flowers in October at 22º49' N, pods ripen in late January. The general recommendation is to harvest 3‒4 weeks after commencement of ripening, when 90‒95% of pods are ripe. While seed yields of >1 t/ha have been recorded, 0.2‒0.5 t/ha are more common.
Set back by the selective grass herbicide, sethoxydim, but recovers with time. In view of its close relationship to Neonotonia wightii, and in the absence of specific information, caution should be exercised using those chemicals that adversely affect that species:
"N. wightii is tolerant of pre-emergence applications of trifluralin and benfluralin. Seedlings are susceptible to acifluorfen, bentazone, 2,4-D and 2,4-DB. Tolerance to 2,4-D and 2,4-DB improves with age. The former should only be used at 0.8 kg/ha a.e. or less once the stand is three to four months old, but still checks growth of the legume. 2,4-DB can be used at five weeks of age at 1.1 kg/ha a.e., and at 2.2 kg/ha a.e. at three to four months. Tolerant of diquat at 140 g/ha cation from 5 to 8 weeks as long as seedlings are healthy, and at 280 g/ha once established."
Eagles, D.A. and Pengelly, B.C. (1996) Morphological and agronomic attributes of a collection of the genus Teramnus. Genetic Resources Communication No. 24. CSIRO Tropical Agriculture, St Lucia, Australia. bit.ly/2X0RnKM
Febles, G. and Funes, F. (1978) Legume development in Cuba. Cuban Journal of Agricultural Science 12:111–124.
Funes, F. and Pérez, C. (1976) Agronomical studies on perennial soybean. I. Comparison between Glycine wightii and Teramnus labialis under cutting and grazing conditions. Cuban Journal of Agricultural Science 10:199–209.
Funes, F. and Yepes, S. (1974) Pasture introduction in Cuba. Proceedings of the XII International Grassland Congress, Moscow, Russia, June 11–20, 1974. p. 89–104.
Gillett, J.B., Polhill, R.M. and Verdcourt, B. (1971) Leguminosae (Part 4) Subfamily Papilionoideae. In: Milne-Redhead, E. and Polhill, R.M. (eds) Flora of Tropical East Africa. Crown Agents for Overseas Governments and Administrations, London, UK. p. 535–538.
González, Y. and Mendoza, F. (1991) Comportamiento de la germinación de Teramnus labialis cv. Semilla clara. II. Tratamientos antes de almacenar. Pastos y Forrajes 14:227–234. bit.ly/2xEJPCO
Gutiérrez, I.R., Pérez, G., Benega, R. and Gómez, L. (2002) Coberturas vivas de leguminosas en el plátano (Musa sp.) 'FHIA-03'. Cultivos Tropicales 23(3):11–17. bit.ly/2xLf7I1
Kaligis, D.A. and Sumolang, C. (1991) Forages species for coconut plantations in North Sulawesi. In: Shelton, H.M. and Stür, W.W. (eds) Forages for Plantation Crops. Proceedings of a workshop, Sanur Beach, Bali, Indonesia. 27–29 June 1990. ACIAR Proceedings No. 32. Australian Centre for International Agricultural Research (ACIAR), Canberra, Australia. p. 45–48. aciar.gov.au/node/8081
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'Semilla Clara' Released in Cuba (pre-1974). Selected from native/naturalized populations in Cuba. The most commonly used cultivar. Terminal leaflet to 5.5 × 2.5 cm, glabrate on the upper surface, hairy underneath; pods pubescent, 3.5‒5 cm long, 2‒3 mm wide, beak 4 mm long; seeds light brown in colour, 7‒10/pod. Flowering early October, and producing pods through to May in the northern hemisphere. Well grazed by cattle.
'Semilla Oscura' Cuba (pre-1974). Selected from native/naturalized populations in Cuba. Shorter internodes than 'Semilla Clara'; terminal leaflet 4 × 2.1 cm, with short hairs on both surfaces; pods slightly hairy, 3.5‒4 cm long, 3 mm wide, beak 2 mm; seeds dark brown or black, 6‒9/pod. Flowers earlier than 'Semilla Clara'.
The folllowing accessions showed merit at 26º S in SE Queensland, Australia on an acid soil, in an area receiving 1,100 mm rainfall. They were evaluated under grazing for persistence and rated for productivity, growing in association with Axonopus fissifolius and Paspalum dilatatum.
CPI 52793 Origin Madagascar (23.08º S, 44.1º E, 300 m asl, rainfall 550 mm).
CPI 52794 Origin Gauteng, South Africa (25.45º S, 28.12º E, 1,300 m asl, rainfall 650 mm).
CPI 52797 Origin Morogoro, Tanzania (7º S, 500 m asl, rainfall 800 mm).
CPI 52799 Origin Arusha, Tanzania (3º S, 1,380 m asl, rainfall 900 mm) - collected from sodic area.
CPI 60371 Origin Krugerspos, South Africa (25º S, 1,120 m asl, rainfall 500 mm).
CPI 60377 Origin Arusha, Tanzania (3º S, 1,390 m asl, rainfall 1,000 mm).
CPI 70292 Selected line from Malkerns Research Station, Swaziland (26º31' S, 780 m asl, rainfall 993 mm).
CPI 82319 Origin Santiago de Cuba (20º N, 50 m asl, rainfall 1,100 mm).
CPI 114122 Origin Ethiopia (11.5º N, 2,900 m asl, rainfall 1,000 mm).
CPI 114123 Origin Ethiopia (11.3º N, 2,960 m asl, rainfall 1,200 mm).