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Phaseolus acutifolius A.Gray

Pl. wright. 1: 43 (1852).
Papilionaceae (Leguminosae - Papilionoideae, Fabaceae)
Chromosome number
2n = 22
Vernacular names
Tepary bean, Texas bean (En). Haricot t้pari, t้pari (Fr). Feijใo tepari (Po).
Origin and geographic distribution
Tepary bean is an ancient crop of the south-western United States and northern Mexico. Recent studies indicate that the earliest remains of domesticated tepary bean, found in Tehuacแn Valley, Mexico, date from around 2300 years ago. Isozyme analysis suggests that domestication took place in a single geographic region, with the Mexican states of Jalisco and Sinaloa being potential candidates. Today, wild types are distributed from the south-western United States (Arizona, New Mexico, Texas) to Guatemala, with the core of their distribution in north-western Mexico. Tepary bean is also cultivated in the southern United States and Central America. Cultivation of tepary bean decreased strongly after World War II, but nowadays the crop is regaining interest. Tepary bean has been introduced and is cultivated in Africa, Asia and Australia. It was introduced into francophone West Africa, Central Africa, East Africa and Madagascar between the first and second World Wars, and is now grown there and as far south as Botswana. Tepary bean is also recorded as being grown in Morocco, Algeria, South Africa, Swaziland and Lesotho.
Tepary bean is mainly grown for its mature dry seeds, which are eaten after boiling, steaming, frying or baking. They are used in stews and soups, and mixed with whole-grain maize. In Uganda the dry seeds are usually boiled and then coarsely ground before being added to soup. Occasionally it is eaten as a green bean or as bean sprouts. The leaves are considered edible in Malawi, but are tougher than those of common bean (Phaseolus vulgaris L.) and take longer to cook. Pods and stems remaining after removing the seed may be used for animal feed. In Botswana the seeds are a common supplementary feed for chickens. Tepary bean has occasionally been grown for fodder or green manure, e.g. in the United States. It may be used as a cover crop and an intercrop in agroforestry systems.
Production and international trade
Tepary bean is mainly grown in Mexico and Arizona (United States). Large-scale commercial production was tried in the early 1900s, but efforts were abandoned due to its unfavourable morphological characteristics compared to the common bean, changes in eating habits and lack of information on its performance. Tepary bean has recently gained importance in semi-arid parts of tropical Africa, e.g. in Sudan, north-eastern Kenya, Uganda and Botswana, where most other grain legumes fail due to drought and where short-duration crops are often needed. Production is mainly for domestic consumption, and no production and trade statistics are available.
Per 100 g edible portion the composition of dry tepary bean seeds is: water 8.6 g, energy 1478 kJ (353 kcal), protein 19.3 g, fat 1.2 g, carbohydrate 67.8 g, fibre 4.8 g, Ca 112 mg, P 310 mg, thiamin 0.33 mg, riboflavin 0.12 mg, niacin 2.8 mg and ascorbic acid 0 mg (Leung, Busson & Jardin, 1968). As with other pulses, the seeds are low in the sulphur-containing amino acids methionine and cystine (0.9–1.3% and 0.8–1.3% of total amino acids, respectively). With respect to antinutritional factors, such as trypsin inhibitors, flatulent oligosaccharides and phytic acid, tepary bean is similar to cowpea and chickpea; the lectin activity is exceptionally high, but is readily reduced by cooking, whereas cyanogenic glucosides have not been detected. Consumption of raw tepary bean flour has been recorded to cause death in mice and rats within 3–4 days, but soaking and cooking the seeds eliminated toxicity completely. Tepary beans have a strong flavour and odour and are less palatable than common beans. On storage the dry seeds become very hard and take a long time to cook. Cultivars with white seeds have a more permeable seedcoat than cultivars with black seeds, resulting in a shorter cooking time.
Tepary bean hay contains 6.6% water, 9.9% protein, 1.9% fat, 43.1% N-free extract, 29.3% fibre, and 9.2% ash. Pods and stems contain 8% water, 4.1% proteins, 0.5% fat, 43.6% N-free extract, 37.0% fibre and 6.8% ash.
Climbing, trailing or more or less erect and bushy annual herb, with stems up to 4 m long; roots fibrous. Leaves alternate, 3-foliolate; stipules lanceolate, 2–3 mm long, appressed to stem; petiole 2–10 cm long; stipels linear, up to 2 mm long; leaflets ovate to ovate-lanceolate, 4–8 cm ื 2–5 cm, acute, usually pubescent below. Inflorescence an axillary raceme, 2–5 flowered. Flowers bisexual, papilionaceous; pedicel 3–7 mm long; calyx campanulate, 3–4 mm long, the upper 2 lobes united into one, the lower 3 triangular; corolla white, pink or pale lilac, standard half-reflexed, broad, emarginate, up to 1 cm long, wings up to 1.5 cm long, keel narrow, coiled; stamens 10, 9 fused and 1 free; ovary superior, c. 0.5 cm long, densely pubescent, style with a thickened terminal coil, with collar of hairs below the stigma. Fruit a compressed pod, straight or slightly curved, 5–9 cm ื 0.5–1 cm, rimmed on margins, with short but distinct beak, hairy when young, 2–9-seeded. Seeds globose to oblong, 4–7(–10) mm ื 2–5(–7.5) mm, white, yellow, brown, purple, black or variously speckled, dull. Seedling with epigeal germination; first pair of leaves simple.
Other botanical information
Phaseolus comprises about 50 species, most of them in the Americas. Three varieties of Phaseolus acutifolius have been distinguished, based on the shape of leaflet and seeds. Var. acutifolius and var. tenuifolius A.Gray comprise wild types from south-western United States and north-western Mexico, whereas var. latifolius G.F.Freeman comprises wild and cultivated types. Isozyme and AFPL analyses have shown no clear-cut differentiation between var. acutifolius and var. tenuifolius.
Growth and development
Tepary bean seeds absorb water easily; in moist soils the testa wrinkles within 5 minutes, in water in 3 minutes. This leads to quick germination. Seedling emergence is faster in white-seeded than in dark-seeded types. The seeds of domesticated types have no dormancy, which is a disadvantage in humid regions, where fallen seeds will germinate rapidly. The rate of germination increases with increasing temperatures from 10ฐC to 35ฐC. Flowering occurs within 27–40 days. Self-pollination occurs before anthesis. In the tropics, short-duration types may mature within 2 months, but most types have a growth period of 70–90 days. In cooler regions, such as coastal Algeria, the growth period averages 120 days. The seeds of many domesticated types of tepary bean are shattered less easily than those of wild types.
Tepary bean shows effective nodulation and nitrogen fixation only with Bradyrhizobium isolates. Hybrids of tepary bean and common bean (the latter nodulating with Bradyrhizobium but only fixing atmospheric nitrogen when nodulated with Rhizobium leguminosarum bv. phaseoli) can be divided in 2 groups: one group only fixing nitrogen with Bradyrhizobium, the other only with Rhizobium leguminosarum bv. phaseoli.
Tepary bean is particularly suited to arid regions as it is tolerant of drought, heat and a dry atmosphere. Factors contributing to the drought tolerance of tepary bean are sensitive stomata, closing already at relatively high water potentials, and a deep and extensive root system. Tepary bean is found in regions with a mean annual temperature of 17–26ฐC; the minimum night temperature should not drop below 8ฐC. It can grow in areas with an annual rainfall ranging from 500–1700 mm, but where annual rainfall exceeds 1000 mm, vegetative growth is usually excessive, at the expense of seed yield. After flowering little or no rain is needed. In most of Africa, tepary bean is grown as a short-season crop, but in the more humid parts it is grown year-round. In Mexico and Arizona it is usually grown at medium altitudes. Some types require short days for flowering, but others seem day-neutral.
Light, well-drained soils are preferred; reasonable yields can be obtained on poor sandy soils with pH 5–7. Tepary bean does not tolerate waterlogging, and heavy clays are unsuitable. It is moderately tolerant of saline and alkaline soils. The salt tolerance may not be physiological but result from its ability to escape salinity due to its root system going deeper than that of e.g. common bean.
Propagation and planting
Tepary bean is propagated by seed. The 1000-seed weight is 100–220 g for cultivated and 15–50 g for wild genotypes. Seeds are broadcast at a rate of 28–34 kg/ha, or drilled in rows 60–90 cm apart with 10–45 cm between plants within the row. The sowing depth is 2.5–10 cm. Tepary bean is sometimes sown on mounds, with 2–4 seeds per mound. In Kenya tepary bean is sown at 15–20 kg/ha in a spacing of 60 cm ื 30 cm. When grown for hay, seed rates are about 70 kg/ha.
Tepary bean is grown as a sole crop or intercropped with cereals (sorghum, millet, maize), vegetables (Allium, Brassica, Capsicum, Cucurbita spp.), or other pulses. In the United States and Mexico tepary bean is sometimes sown in unsorted admixtures with common bean, thus providing greater yield stability than common bean alone and higher potential yields than tepary bean alone.
Weeding of tepary bean is essential, particularly during early growth. It requires little weeding, however, when it is grown as an ‘end-of-season’ crop. Little is known about its nutrient requirements, and its response to nitrogen and potassium fertilizers is not consistent. Irrigation may be applied, but is not usual. In intercropping the cultural practices for the main crop are applied to tepary bean. In Senegal and Mali tepary bean is grown as a kitchen garden vegetable.
Diseases and pests
Tepary bean is generally not affected by diseases in semi-arid regions, except during periods when humidity is high. Within the species, variable levels of resistance exist against common bacterial (bean) blight (Xanthomonas campestris pv. phaseoli), bean rust (Uromyces appendiculatus), Fusarium rot (Fusarium sp.), powdery mildew (Erysiphe polygoni), anthracnose (Colletotrichum lindemuthianum), angular leaf spot (Phaeoisariopsis griseola) and charcoal rot (Macrophomina phaseolina). Tepary bean is susceptible to white mould disease (Sclerotinia sclerotiorum) and also considered susceptible to halo blight (Pseudomonas syringae pv. phaseolicola); it is listed as a host of southern blight (Sclerotium rolfsii) and Pythium rot (Pythium aphanidermatum). Tepary bean is highly susceptible to bean common mosaic virus (BCMV), and also has shown susceptibility to alfalfa mosaic virus (AMV), bean yellow mosaic virus (BYMV), beet curly top virus (BCTV), bean pod mottle virus (BPMV) and bean golden mosaic virus (BGMV).
Leafhoppers (Empoasca kraemeri) and pod borers (Epinotia opposita) were found in water-stressed trials. Several lines have shown resistance against the former, but the mechanism was non-preference rather than antibiosis. The Mexican bean beetle (Epilachna varivestis) and the potato leafhopper (Empoasca fabae) have been found to cause damage to tepary bean. Some resistance to the black bean aphid (Aphis fabae) and the lesser corn stalk borer (Elasmopalpus lignosellus) has been observed. The hard seed coat makes the seed resistant to storage pests such as bruchid beetles (Callosobruchus and Acanthoscelides spp.). In Uganda, however, the rice weevil (Sitophilus oryzae) has been recorded in stored seed.
Pods on the same tepary bean plant do not usually mature simultaneously, and as pods may shatter if left to dry up in the field, they are normally harvested by hand as soon as they change colour, usually 2.5–3 months after planting. Sometimes whole plants are pulled up by hand. Normally the pods are dried for a few days before they are threshed. In Africa beating the dried pods or plants with sticks is common practice to thresh tepary bean.
In Uganda average yields of tepary bean are 450–670 kg dry seeds per ha. In dry-land farming in the United States yields are 500–800 kg/ha, under irrigation 900–1700 kg/ha. When grown for fodder, 5500–11,000 kg/ha oven-dry hay can be obtained.
Handling after harvest
Unlike most other pulses, tepary bean seed stores well and it hardly needs storage pest control.
Genetic resources
The genetic basis of cultivated tepary bean is narrower than that of cultivated common bean and Lima bean (Phaseolus lunatus L.), and most genetic diversity for future improvement resides in the wild types. Collection of germplasm from the native area of tepary bean is recommended. Wild tepary bean genepools have decreased due to habitat elimination and degradation, whereas domesticated tepary bean has suffered genetic erosion due to its shrinking area of cultivation. Exchange of genetic information between common bean and tepary bean is possible, but only for the transfer of simple traits involving only a few genes. Although common bean and tepary bean have the same chromosome number and similar karyotypes their mitochondrial genomes, agro-ecological adaptations and morphological characters are distinct, indicating that they are fairly divergent species.
The largest germplasm collection of tepary bean (about 350 accessions) is held at CIAT (Centro Internacional de Agricultura Tropical) in Cali, Colombia. Another large collection is present at the USDA-ARS Western Regional Plant Introduction Station, Pullman, Washington, United States (211 accessions). Smaller collections are held in Australia (Australian Tropical Crops & Forages Genetic Resources Centre, Biloela; 70 accessions), Belgium (National Botanical Garden of Belgium, Meise; 59 accessions), Mexico (Instituto Nacional de Investigaciones Forestales, Agrํcolas y Pecuarias (INIFAP), Col. San Rafael; 40 accessions) and Guatemala (Centro Universitario de Sur Occidente (CUNSUROC), Universidad de San Carlos, Mazatenango; 31 accessions). In Africa, 29 accessions are held at ISRA (Institut S้n้galais de Recherches Agricoles), Dakar, Senegal, and 10 accessions at ILRI (International Livestock Research Institute), Addis Ababa, Ethiopia. Most collections comprise wild as well as cultivated types.
Tepary bean is generally resistant to diseases and pests, tolerant to drought, heat and salinity and has a short crop cycle. Prospects for selection are favourable, as sufficient variation in resistance to biotic and abiotic stress factors exists within the species. Except for some mass-selected populations, no improved tepary bean cultivars have been released to farmers. Rather, its favourable traits have mainly been targeted to improve common bean instead of tepary bean itself. Resistance to common bacterial (bean) blight, for instance, has been transferred into common bean through interspecific hybridization. In attempts to cross Phaseolus acutifolius with Phaseolus vulgaris, artificial cross-fertilization does not pose problems, but post-zygotic barriers usually prevent normal embryo development, and, as a rule, no viable hybrids are obtained. Embryo rescue through in-vitro culture is normally required to complete hybridization successfully. Through recurrent backcrossing with alternating parents the hybrids become cross-fertile with both species. However, genes obtained from common bean tend to be predominant in these hybrids. Seeds have also been obtained from a cross involving a Phaseolus acutifolius accession (NI 576) without in-vitro culture. Agrobacterium-mediated genetic transformation of this accession has been achieved, based on regeneration from callus. This has opened up the possibility of using Phaseolus acutifolius to introduce transgenes into the economically more important Phaseolus vulgaris.
Tepary bean seems a very suitable crop for resource-poor farmers in Africa, since its rapid germination, deep root system and short life cycle make it well adapted for production in arid or semi-arid regions. Reasons for reluctance to adopt tepary bean as a food include the small seed size, the tendency to cause flatulence, the long cooking time, the laboriousness of the harvest, and its strong flavour and, according to some, objectionable odour. However, in northern Kenya and Nigeria, traditional dishes prepared with tepary bean instead of cowpea were found very acceptable. To promote tepary bean in Africa, the selection of high-yielding cultivars, the development of food products (protein supplements) with reduced odour, and the creation of a marketing infrastructure are a prerequisite.
Major references
• CIAT, 2003. Bean improvement for the tropics. Project IP-1. Annual Report 2002. Centro Internacional de Agricultura Tropical (CIAT), Cali, Colombia.
• Dillen, W., de Clercq, J., Goossens, A., van Montagu, M. & Angenon, G., 1997. Agrobacterium mediated transformation of Phaseolus acutifolius A. Gray. Theoretical and Applied Genetics 94(2): 151–158.
• Hornetz, B., 1993. On the development and acceptance of agropastoral (agrosilvipastoral) systems in the semiarid areas of northern Kenya. In: Baum, E., Wolff, P. & Z๖bisch, M.A. (Editors). Acceptance of soil and water conservation strategies and technologies. Topics in applied resource management in the tropics. Volume 3. pp. 413–453.
• Jansen, P.C.M., 1989. Phaseolus acutifolius A. Gray. In: van der Maesen, L.J.G. & Somaatmadja, S. (Editors). Plant Resources of South-East Asia No 1. Pulses. Pudoc, Wageningen, Netherlands. pp. 54–55.
• Kaplan, L. & Lynch, T.F., 1999. Phaseolus (Fabaceae) in archaeology: AMS radiocarbon dates and their significance for pre-Colombian agriculture. Economic Botany 53(3): 261–272.
• Kay, D.E., 1979. Food legumes. Crops and Product Digest No 3. Tropical Products Institute, London, United Kingdom. 435 pp.
• Miklas, P.N., Rosas, J.C., Breaver, J.S., Telek, L. & Freytag, G.F., 1994. Field performance of selected tepary bean germplasm in the tropics. Crop Science 34: 1639–1644.
• National Academy of Sciences, 1979. Tropical legumes: resources for the future. National Academy of Sciences, Washington, D.C., United States. 331 pp.
• Pratt, R.C. & Nabhan, G.P., 1988. Evolution and diversity of Phaseolus acutifolius genetic resources. In: Gepts, P. (Editor). Genetic resources of Phaseolus beans: their maintenance, domestication, evolution, and utilization. Kluwer Academic Publishers, Dordrecht, Netherlands. pp. 409–440.
• Tinsley, A.M., Scheerens, J.C., Alegbejo, J.O., Adan, F.H., Krumhar, K.C., Butler, L.E. & Kopplin, M.J., 1985. Tepary beans (Phaseolus acutifolius var. latifolius): a potential food source for African and Middle Eastern cultures. Qualitas Plantarum: Plant Foods for Human Nutrition 35(2): 87–101.
Other references
• Aganga, A.A., Omphile, U.J., Malope, P., Chabanga, C.H., Motsamai, G.M. & Motsumi, L.G., 2000. Traditional poultry production and commercial broiler alternatives for small-holder farmers in Botswana. Livestock Research for Rural Development 12(4): 1–8.
• Baudoin, J.P. & Maquet, A., 1999. Improvement of protein and amino acid contents in seeds of food legumes. A case study in Phaseolus. BASE, Biotechnologie, Agronomie, Soci้t้ et Environnement 3(4): 220–224.
• Debouck, D.G. & Smartt, J., 1995. Beans. In: Smartt, J. & Simmonds, N.W. (Editors). Evolution of crop plants. 2nd Edition. Longman, London, United Kingdom. pp. 287–294.
• Freytag, G. & Debouck, D.G., 2002. Taxonomy, distribution and ecology of the genus Phaseolus (Leguminosae - Papilionoideae) in North America, Mexico and Central America. Botanical Institute of Texas, Fort Worth, Texas, United States. 300 pp.
• Garvin, D.F. & Weeden, N.F., 1994. Isozyme evidence supporting a single geographic origin for domesticated tepary bean. Crop Science 34(5): 1390–1395.
• Idouraine, A., Tinsley, A.M. & Weber, C.W., 1989. Nutritional quality and sensory acceptability of akara prepared from germinated tepary beans. Journal of Food Science 54(1): 114–117.
• Idouraine, A., Weber, C.W. & Kohlhepp, E.A., 1995. Composition of tepary bean (Phaseolus acutifolius) of the southwestern US and northern Mexico. Ecology of Food and Nutrition 33(3): 139–147.
• Kaiser, W.J., 1981. Diseases of chickpea, lentil, pigeon pea, and tepary bean in continental United States and Puerto Rico. Economic Botany 35(3): 300–320.
• Leung, W.-T.W., Busson, F. & Jardin, C., 1968. Food composition table for use in Africa. FAO, Rome, Italy. 306 pp.
• Lin, T.Y. & Markhart III, A.H., 1996. Phaseolus acutifolius A. Gray is more heat tolerant than P. vulgaris L. in the absence of water stress. Crop Science 36(1): 110–114.
• Markhart III, A.H., 1985. Comparative water relations of Phaseolus vulgaris L. and Phaseolus acutifolius Gray. Plant Physiology 77(1): 113–117.
• Mogotsi, K.K., 1982. Evaluation of factors influencing growth, development and yield of grain legumes. MSc Thesis, Texas Tech University, Lubbock, Texas, United States. 83 pp.
• Mu๑oz, L.C., Blair, M.W., Duque, M.C., Tohme, J. & Roca, W., 2004. Introgression in common bean ื tepary bean interspecific congruity-backcross lines as measured by AFPL markers. Crop Science 44 (2): 637–645.
• Nabhan, G.P. & Felger, R.S., 1978. Teparies in southwestern North America. A biogeographical and ethnohistorical study of Phaseolus acutifolius. Economic Botany 32(1): 2–19.
• Purseglove, J.W., 1968. Tropical Crops. Dicotyledons. Longman, London, United Kingdom. 719 pp.
• Schinkel, C. & Gepts, P., 1988. Phaseolin diversity in the tepary bean, Phaseolus acutifolius A. Gray. Plant Breeding 101(4): 292–301.
• Somasegaran, P., Hoben, H.J. & Lewinson, L., 1991. Symbiotic interactions of Phaseolus acutifolius and P. acutifolius ื P. vulgaris hybrid progeny in symbiosis with Bradyrhizobium spp. and Rhizobium leguminosarum bv. phaseoli. Canadian Journal of Microbiology 37(7): 497–503.
• Stanton, W.R., 1966. Grain legumes in Africa. FAO, Rome, Italy. 183 pp.
• Thorn, K.A., Tinsley, A.M., Weber, C.W. & Berry, J.W., 1983. Antinutritional factors in legumes of the Sonoran desert. Ecology of Food and Nutrition 13(4): 251–256.
• White, J.W. & Montes, R.C., 1993. The influence of temperature on seed germination in cultivars of common bean. Journal of Experimental Botany 44(269): 1795–1800.
Sources of illustration
• Jansen, P.C.M., 1989. Phaseolus acutifolius A. Gray. In: van der Maesen, L.J.G. & Somaatmadja, S. (Editors). Plant Resources of South-East Asia No 1. Pulses. Pudoc, Wageningen, Netherlands. pp. 54–55.
• K.K. Mogotsi
Botswana College of Agriculture, Private Bag 0027, Gaborone, Botswana

• M. Brink
PROTA Network Office Europe, Wageningen University, P.O. Box 341, 6700 AH Wageningen, Netherlands
• G. Belay
Ethiopian Agricultural Research Organization, Debre Zeit Center, P.O. Box 32, Debre Zeit, Ethiopia
Associate editors
• J.M.J. de Wet
Department of Crop Sciences, Urbana-Champaign, Turner Hall, 1102 South Goodwin Avenue, Urbana, IL 61801, United States
• O.T. Edje
Faculty of Agriculture, University of Swaziland, P.O. Luyengo, Luyengo, Swaziland
• E. Westphal
Ritzema Bosweg 13, 6706 BB Wageningen, Netherlands
General editors
• R.H.M.J. Lemmens
PROTA Network Office Europe, Wageningen University, P.O. Box 341, 6700 AH Wageningen, Netherlands
• L.P.A. Oyen
PROTA Network Office Europe, Wageningen University, P.O. Box 341, 6700 AH Wageningen, Netherlands
Photo editor
• A. de Ruijter
PROTA Network Office Europe, Wageningen University, P.O. Box 341, 6700 AH Wageningen, Netherlands

Correct citation of this article:
Mogotsi, K.K., 2006. Phaseolus acutifolius A.Gray In: Brink, M. & Belay, G. (Editors). PROTA 1: Cereals and pulses/C้r้ales et l้gumes secs. [CD-Rom]. PROTA, Wageningen, Netherlands.
Distribution Map planted

1, flowering branch with young fruit; 2, fruits; 3, seeds.
Source: PROSEA

plant habit