Pages

“Many people praise and acknowledge the healing power of plants, but few people actually take action to prevent their extension by planting and conserving them for future generations.” (Ernest Rukangira )

Monday, 10 March 2014

Fwd: Bitter leaf, delightful soup, cure for malaria?




Bitter leaf, delightful soup, cure for malaria?

March 12, 2012 | Filed under: Feature | Posted by:

Maybe the cure for malaria is closer than anyone can imagine. Scientists looking into potential sources of cure for malaria have identified bitter leaf, a very popular soup vegetable, as a possible ingredient for the treatment of malaria  in future.

The leaves of Vernonia amygdalina, popularly known as bitter leaf, are usually bitter and all parts of the plant (leaves, stem and roots) are said to have medicinal uses. These include promotion of dieresis, cure of tonsillitis, fever,  diabetes, pneumonia, jaundice, anaemia, stomach problem and ascaris.

In a study, researchers studied the antimalarial activities of the aqueous and ethanolic crude extracts of bitter leaves, already in use by traditional healers to treat malaria and other diseases.

The researchers found that under laboratory conditions, extracts of bitter leaf made from water and ethanol showed moderate antimalarial activity and a negligible level of toxicity in the test animals–rats.

Malaria is one of the most important tropical diseases and the greatest cause of hospitalisation and death among children below age of five years. The World Health Organisation (WHO) reported that there were an estimated 246 million malaria cases distributed among 3.3 billion people at risk in 2006, causing at least a million deaths. These were mostly children under five years.

WHO said approximately 80 per cent of malaria cases in the world are estimated to be in Africa where the disease is endemic. In Nigeria, malaria transmission occurs all-year-round in the South, and is more seasonal in the North.

The alarming rate at which Plasmodium falciparum has developed resistance to chloroquine and other synthetic antimalarial drugs makes it necessary to search for more effective antimalarial compounds.

In Africa and other countries where malaria is endemic, traditional medicinal plants are frequently used to treat or cure malaria, thus the need to investigate the antimalarial activity of medicinal plants in order to determine their potentials as sources of new antimalarial agents.

The study entitled “In vitro Antimalarial Activity of the Extracts of Vernonia Amygdalina” was documented in the 2011 edition of the Science World Journal. It was carried out by Sha’a, K. K from the College of Science and Technology, Adamawa State Polytechnic; Oguche, S from the Department of Paediatrics, Jos University Teaching Hospital, Jos; Watila, I. M from the Department of Paediatrics, State Specialist Hospital, Maiduguri, Borno State, as well as Ikpa, T. F. from the Department of Wildlife, University of Agriculture, Makurdi.

For the study, blood samples were collected from children and adults aged six months and above, who had fever in the last 24 hours, auxiliary temperature of 37.5 C, had not taken any antimalarial in the last two weeks, and who gave oral or written informed consent after the aim of the study were involved in the study. These were patients attending the outpatient department of the Damboa General Hospital, Borno State.

Of the two extracts tested, the ethanol extract of bitter leave showed the highest antimalarial activity of 78.1 per cent. The water extract had the malaria parasite growth inhibition of 74.0 per cent.

In addition, dose-dependent antimalarial activity was clearly shown for the two crude extracts. The percentage inhibitions are higher with increasing concentrations.

Previously, the antimalarial activity of bitter leaf against resistant P. berghei had been reported by scientists in the British Journal of Biomedical Science. In their findings, leaf extract produced 67 per cent suppression of malaria –causing germ in a four day test.

In addition, a another study pointing to the potential use of bitter leaf in formulating a malaria drug in years to come, revealed its potential also in reversing chloroquine resistance when used as an adjuvant with chloroquine.

The 2008 study, documented in the journal African Health Sciences, while validating the traditional use of bitter leave  in the treatment of malaria in Nigeria reported that the aqueous extract of the plant enhance the antimalarial effects chloroquine in mice infected with chloroquine resistant and sensitive P. berghei strains.

Previously, a 2010 study documented in the African Journal of Traditional, Complementary and Alternative Medicines stated that African mahogany, in combination with chloroquine or halofantrine, elicited significantly greater malaria parasite clearance following the administration of the combination when compared to the effects of African mahogany or the conventional drugs alone.

The study  was entitled “Chemotherapeutic interaction between Khaya Grandifoliola stem bark extract and two anti-malarial drugs in mice.” It was carried out by Steve O Ijarotimi; Joseph M Agbedahunsi; Clement O Adewunmi and Cyprian O Onyeji, all researchers at the Obafemi Awolowo University, Ile-Ife, Osun State.

Similarly, a review of studies into medicinal plants used to treat malaria across all ethnic and cultural groups in Nigeria showed that there were more than 110 plant varieties. The review entitled: “Medicinal plants used in Nigeria for treatment of malaria” was documented by the 2011 edition in the Journal of Ethnopharmacology. It involved J.O Adebayo from the Department of Biochemistry, University of Ibadan in collaboration with A.U Krettlia.

They include plants such as leaves of Newbouldia laevis (Akoko leaf in Yoruba), Enatia chlorantha (African yellow wood, Iyani or Awopa in Yoruba), Eupatorium odoratum (ogbogbo or Ibo- ofo in Yoruba), Bridelia micrantha (abere-aluko or akisan in Yoruba), Cajanus Cajan (Pigeon pea in English, olele in Edo, shingwazo in Gwari), Carica papaya (pawpaw).

In addition, there were also stem bark of plants such as Abrus precatorius (omisinmisin in Yoruba), Afzelia Africana (Mohogany bean tree), Psidium guajava (guava), cashew plant, Blighia sapida (Achee, Akee, Akee or Apple Tree), Alchornea cordifolia (baushe in Hausa, edo in Igbo and idi-odan in Yoruba). Also on the list were stems of Citrus sinensis (sweet orange), Cymbopogon giganteus (Oka eye in Yoruba), Khaya senegalensis (African mahogany, madachi in Hausa and ono in Igbo), Mangifera indica (mango) as well as onion bulbs and ginger.

Alstonia boonei (awun in Yoruba) is highly priced, especially in situations where affordable antimalarial drugs are found ineffective, due to drug-resistant malaria parasites. The plant stem bark or leaves are administered as decoction or “teas” and sometimes as an ingredient in malaria “steam therapy”.

Recently, researchers in the 2008 edition of Tropical Journal of Pharmaceutical Research, formulated the stem bark extract of this plant into tablets, and made this available as an antimalarial remedy.

Most of these antimalarial plants are used in form of monotherapy, and only a few plants are taken together in combined therapies. An example is the multi-herbal extract referred to as ‘Agbo-Iba’ made up of Cajanus cajan (pigeon pea) leaf, Euphorbia lateriflora leaf, mango leaf and bark, Cassa alata leaf(Asunwon in Yoruba), Cymbopogon giganteus leaf, Nauclea latifolia leaf, and Uvaria chamae bark.

Pharmacological studies have demonstrated under laboratory conditions antimalarial effects of extracts from 45 plant species used in Nigerian folk medicine out of the 51 species tested. These include neem, Morinda lucida (brimstone tree, oruwo in Yoruba and eze-ogu in Igbo), African mahogany, Tithonia diversifolia (Wild Sunflower; ogbo or Agbale in Yoruba), Momordica balsamina (Balsam pear or ejinrin in Yoruba) and Picralima nitida (abere in Yoruba).

Previous studies on neem, attributed its antimalarial effect to it affecting all stages of the malaria parasite in the body unlike artemisinin and primaquine that seem to affect only the immature stages of the malaria parasite.

It should be noted, however, that some of these extracts exhibited very high antimalarial activity in laboratory tests carried out on the malaria germ in the test tube, but displayed poor activity in animals infected with malaria germ.
 

Fwd: Bitter leaf, delightful soup, cure for malaria?




Bitter leaf, delightful soup, cure for malaria?

March 12, 2012 | Filed under: Feature | Posted by:

Maybe the cure for malaria is closer than anyone can imagine. Scientists looking into potential sources of cure for malaria have identified bitter leaf, a very popular soup vegetable, as a possible ingredient for the treatment of malaria  in future.

The leaves of Vernonia amygdalina, popularly known as bitter leaf, are usually bitter and all parts of the plant (leaves, stem and roots) are said to have medicinal uses. These include promotion of dieresis, cure of tonsillitis, fever,  diabetes, pneumonia, jaundice, anaemia, stomach problem and ascaris.

In a study, researchers studied the antimalarial activities of the aqueous and ethanolic crude extracts of bitter leaves, already in use by traditional healers to treat malaria and other diseases.

The researchers found that under laboratory conditions, extracts of bitter leaf made from water and ethanol showed moderate antimalarial activity and a negligible level of toxicity in the test animals–rats.

Malaria is one of the most important tropical diseases and the greatest cause of hospitalisation and death among children below age of five years. The World Health Organisation (WHO) reported that there were an estimated 246 million malaria cases distributed among 3.3 billion people at risk in 2006, causing at least a million deaths. These were mostly children under five years.

WHO said approximately 80 per cent of malaria cases in the world are estimated to be in Africa where the disease is endemic. In Nigeria, malaria transmission occurs all-year-round in the South, and is more seasonal in the North.

The alarming rate at which Plasmodium falciparum has developed resistance to chloroquine and other synthetic antimalarial drugs makes it necessary to search for more effective antimalarial compounds.

In Africa and other countries where malaria is endemic, traditional medicinal plants are frequently used to treat or cure malaria, thus the need to investigate the antimalarial activity of medicinal plants in order to determine their potentials as sources of new antimalarial agents.

The study entitled “In vitro Antimalarial Activity of the Extracts of Vernonia Amygdalina” was documented in the 2011 edition of the Science World Journal. It was carried out by Sha’a, K. K from the College of Science and Technology, Adamawa State Polytechnic; Oguche, S from the Department of Paediatrics, Jos University Teaching Hospital, Jos; Watila, I. M from the Department of Paediatrics, State Specialist Hospital, Maiduguri, Borno State, as well as Ikpa, T. F. from the Department of Wildlife, University of Agriculture, Makurdi.

For the study, blood samples were collected from children and adults aged six months and above, who had fever in the last 24 hours, auxiliary temperature of 37.5 C, had not taken any antimalarial in the last two weeks, and who gave oral or written informed consent after the aim of the study were involved in the study. These were patients attending the outpatient department of the Damboa General Hospital, Borno State.

Of the two extracts tested, the ethanol extract of bitter leave showed the highest antimalarial activity of 78.1 per cent. The water extract had the malaria parasite growth inhibition of 74.0 per cent.

In addition, dose-dependent antimalarial activity was clearly shown for the two crude extracts. The percentage inhibitions are higher with increasing concentrations.

Previously, the antimalarial activity of bitter leaf against resistant P. berghei had been reported by scientists in the British Journal of Biomedical Science. In their findings, leaf extract produced 67 per cent suppression of malaria –causing germ in a four day test.

In addition, a another study pointing to the potential use of bitter leaf in formulating a malaria drug in years to come, revealed its potential also in reversing chloroquine resistance when used as an adjuvant with chloroquine.

The 2008 study, documented in the journal African Health Sciences, while validating the traditional use of bitter leave  in the treatment of malaria in Nigeria reported that the aqueous extract of the plant enhance the antimalarial effects chloroquine in mice infected with chloroquine resistant and sensitive P. berghei strains.

Previously, a 2010 study documented in the African Journal of Traditional, Complementary and Alternative Medicines stated that African mahogany, in combination with chloroquine or halofantrine, elicited significantly greater malaria parasite clearance following the administration of the combination when compared to the effects of African mahogany or the conventional drugs alone.

The study  was entitled “Chemotherapeutic interaction between Khaya Grandifoliola stem bark extract and two anti-malarial drugs in mice.” It was carried out by Steve O Ijarotimi; Joseph M Agbedahunsi; Clement O Adewunmi and Cyprian O Onyeji, all researchers at the Obafemi Awolowo University, Ile-Ife, Osun State.

Similarly, a review of studies into medicinal plants used to treat malaria across all ethnic and cultural groups in Nigeria showed that there were more than 110 plant varieties. The review entitled: “Medicinal plants used in Nigeria for treatment of malaria” was documented by the 2011 edition in the Journal of Ethnopharmacology. It involved J.O Adebayo from the Department of Biochemistry, University of Ibadan in collaboration with A.U Krettlia.

They include plants such as leaves of Newbouldia laevis (Akoko leaf in Yoruba), Enatia chlorantha (African yellow wood, Iyani or Awopa in Yoruba), Eupatorium odoratum (ogbogbo or Ibo- ofo in Yoruba), Bridelia micrantha (abere-aluko or akisan in Yoruba), Cajanus Cajan (Pigeon pea in English, olele in Edo, shingwazo in Gwari), Carica papaya (pawpaw).

In addition, there were also stem bark of plants such as Abrus precatorius (omisinmisin in Yoruba), Afzelia Africana (Mohogany bean tree), Psidium guajava (guava), cashew plant, Blighia sapida (Achee, Akee, Akee or Apple Tree), Alchornea cordifolia (baushe in Hausa, edo in Igbo and idi-odan in Yoruba). Also on the list were stems of Citrus sinensis (sweet orange), Cymbopogon giganteus (Oka eye in Yoruba), Khaya senegalensis (African mahogany, madachi in Hausa and ono in Igbo), Mangifera indica (mango) as well as onion bulbs and ginger.

Alstonia boonei (awun in Yoruba) is highly priced, especially in situations where affordable antimalarial drugs are found ineffective, due to drug-resistant malaria parasites. The plant stem bark or leaves are administered as decoction or “teas” and sometimes as an ingredient in malaria “steam therapy”.

Recently, researchers in the 2008 edition of Tropical Journal of Pharmaceutical Research, formulated the stem bark extract of this plant into tablets, and made this available as an antimalarial remedy.

Most of these antimalarial plants are used in form of monotherapy, and only a few plants are taken together in combined therapies. An example is the multi-herbal extract referred to as ‘Agbo-Iba’ made up of Cajanus cajan (pigeon pea) leaf, Euphorbia lateriflora leaf, mango leaf and bark, Cassa alata leaf(Asunwon in Yoruba), Cymbopogon giganteus leaf, Nauclea latifolia leaf, and Uvaria chamae bark.

Pharmacological studies have demonstrated under laboratory conditions antimalarial effects of extracts from 45 plant species used in Nigerian folk medicine out of the 51 species tested. These include neem, Morinda lucida (brimstone tree, oruwo in Yoruba and eze-ogu in Igbo), African mahogany, Tithonia diversifolia (Wild Sunflower; ogbo or Agbale in Yoruba), Momordica balsamina (Balsam pear or ejinrin in Yoruba) and Picralima nitida (abere in Yoruba).

Previous studies on neem, attributed its antimalarial effect to it affecting all stages of the malaria parasite in the body unlike artemisinin and primaquine that seem to affect only the immature stages of the malaria parasite.

It should be noted, however, that some of these extracts exhibited very high antimalarial activity in laboratory tests carried out on the malaria germ in the test tube, but displayed poor activity in animals infected with malaria germ.
 

Fwd:




Digitaria exilis (Kippist) Stapf

Protologue
Bull. Misc. Inform. Kew 1915: 385 (1915).
Family
Poaceae (Gramineae)
Chromosome number
2n = 54
Vernacular names
Fonio, hungry rice, white fonio (En). Fonio, fonio blanc, petit mil (Fr).
Origin and geographic distribution
Fonio is only known from cultivation and its exact origin is unknown, but it is of ancient cultivation in West Africa. It may have derived from Digitaria longiflora (Retz.) Pers. in the inland delta region of the Niger. Historical records of the use of fonio as a cereal go back to the 14th century. Nowadays fonio is grown scattered from Cape Verde and Senegal to Lake Chad, especially on the Fouta Djallon Plateau in Guinea, the Bauchi Plateau in Nigeria and in north-western Benin. It is also grown in the Dominican Republic.
Uses
Fonio is a staple food in various parts of West Africa, where it is also known as ‘acha’ or ‘fundi’, but it is also a prestige food (‘chief’s food’) and a gourmet item. In the Hausa regions of Nigeria, Benin, Togo and Ghana, special couscous types (‘wusu-wusu’) are prepared with fonio. In southern Togo, the Akposso and Akebou people prepare fonio with beans in a dish for special occasions. In Nigeria fonio flour is made into thick, unfermented porridges (‘tuwo acha’), and fermented grains are used for thin porridges (‘kunu acha’). Boiled whole grains are eaten with vegetables, fish or meat. In northern Togo, the Lamba people brew beer (‘tchapalo’) from fonio. It is also popped and can be mixed with other flours to make bread. In the Dominican Republic fonio flour is made into porridges and creams, mixed with other cereal flours to make cookies, and it is used in the preparation of candy and fermented beverages; aside from everyday meals, fonio is also associated with various religious festivities inherited from African ancestors.
Fonio grain is a valuable, easily digested feed for farm animals. The straw and chaff are excellent fodder and are often sold in markets for this purpose. Chopped fonio straw is mixed with clay to build walls of houses. The straw is also used as fuel for cooking or to produce ash for potash. Fonio grain is considered to have medicinal properties; it is recommended for lactating women and diabetic people.
Production and international trade
According to FAO statistics the average world production of fonio (the major share) and black fonio (Digitaria iburua Stapf) together in 1999–2003 amounted to 257,000 t per year from 360,000 ha, all in West Africa. The main producing countries are Guinea (128,000 t per year in 1999–2003, from 137,000 ha), Nigeria (78,000 t from 142,000 ha), Mali (21,000 t from 33,000 ha), Burkina Faso (13,000 t from 16,000 ha) and Côte d’Ivoire (11,000 t from 22,000 ha). The production in the Dominican Republic is not known. FAO statistics show an increase in world production from around 180,000 t per year in the early 1960s to around 260,000 t in the early 2000s, with an increase in acreage from around 280,000 ha to about 360,000 ha. Fonio is hardly traded outside West Africa, except for small quantities sold as luxury product in Europe.
Properties
The composition of whole fonio grain per 100 g edible portion is: water 11.2 g, energy 1390 kJ (332 kcal), protein 7.1 g, fat 3.0 g, carbohydrate 74.4 g, fibre 7.4 g, Ca 41 mg, P 191 mg, Fe 8.5 mg, thiamin 0.24 mg, riboflavin 0.10 mg and niacin 1.9 mg (Leung, Busson & Jardin, 1968). The essential amino-acid content per 100 g grain is: tryptophan 111 mg, lysine 205 mg, methionine 441 mg, phenylalanine 402 mg, threonine 315 mg, valine 457 mg, leucine 772 mg and isoleucine 315 mg (FAO, 1970). The amino acid composition of fonio is comparable with that of other cereals, but it has a relatively high methionine content. The palatability of fonio grain is considered high.
Adulterations and substitutes
Black fonio and Guinea millet (Brachiaria deflexa (Schumach.) Robyns) are used as substitutes of fonio.
Description
Ascending, free-tillering annual grass up to 80 cm tall, with delicate kneed stems. Leaves alternate, simple; leaf sheath glabrous, smooth, striate; ligule membranous, broad, c. 2 mm long; blade linear to lanceolate, gradually tapering to an acute apex, 5–15 cm × 0.3–0.9 cm, glabrous. Inflorescence a terminal digitate panicle of 2–5 slender, spike-like primary branches up to 15 cm long. Spikelet up to 1 mm stalked, narrowly ellipsoid, 1.5–2 mm long, acute, glabrous, pale green, 2-flowered; lower glume hyaline, minute, upper glume broadly oblong, slightly shorter than spikelet, hyaline between the 3–5 green veins; lower floret sterile, upper floret bisexual; lemma about as long as spikelet, 7–9-veined; palea slightly shorter than lemma; stamens 3; ovary superior, with 2 stigmas. Fruit a caryopsis (grain), oblong to globose-ellipsoid, c. 0.5 mm long, white to pale brown or purplish.
Other botanical information
Digitaria is a taxonomically difficult genus comprising about 230 species in tropical, subtropical and warm-temperate regions, particularly in the Old World. Digitaria barbinodis Henr., occurring in Mali and Nigeria, is harvested as a wild cereal during times of scarcity and is occasionally grown in Nigeria. Digitaria ciliaris (Retz.) Koeler is sometimes eaten as a supplementary food (Chad) or as a famine food. Digitaria debilis (Desf.) Willd., Digitaria fuscescens (Presl) Henrard, Digitaria leptorhachis (Pilg.) Stapf, Digitaria longiflora (Retz.) Pers., Digitaria nuda Schumach. and Digitaria ternata (A.Rich) Stapf are also known to be eaten as famine foods in tropical Africa, but are considered more important as forage or auxiliary plant. In India (Assam) and Vietnam Digitaria cruciata (Nees ex Steud.) A.Camus (‘raishan’) is grown for food and fodder, whereas Digitaria sanguinalis (L.) Scop. (‘crabgrass’) is or was grown as a cereal in Europe, Asia and America.
Diversity within Digitaria exilis is broad, with a large number of locally cultivated landraces, differing in plant habit, plant colour, glume colour, grain size and length of the crop cycle. Based on morphology, 5 varieties have been distinguished:
– var. gracilis Portères: leaf margin curled, inflorescence with 2 primary branches, each with 50–100 spikelets per 10 cm, spikelets in groups of (2–)3(–4) and in 1–2 rows, stalks rough; early-maturing; Kankan region (Guinea).
– var. stricta Portères: leaf margin slightly curled, inflorescence with 2 primary branches, each with 50–100 spikelets per 10 cm, spikelets in groups of (2–)3(–4) and mostly in 1 row, stalks smooth; early-maturing; Casamance (Senegal), Guinea, Mali and Burkina Faso.
– var. rustica Portères: robust plants, inflorescence with (2–)3–4(–5) primary branches, each with 90–120 spikelets per 10 cm, spikelets in groups of (3–)4 and in 2–3 rows, stalks smooth; late-maturing; Casamance (Senegal), Guinea, Mali and Burkina Faso.
– var. mixta Portères: robust plants, vegetative parts reddish pigmented, inflorescence with ( 2–)3–4(–5) primary branches, each with 90–120 spikelets per 10 cm, spikelets in groups of (3–)4 and in 2–3 rows, stalks smooth; late-maturing; Guinea.
– var. densa Portères: tall, strong plants, with a long vegetative cycle, inflorescence with 3–4 primary branches, each with 120–140 spikelets per 10 cm, spikelets in groups of 2(–3) and in 2–3 rows; late-maturing; Togo.
Growth and development
Fonio normally germinates 2–4 days after sowing and grows rapidly. Flowering usually occurs 6–8 weeks after emergence. The time from sowing to maturity is normally 2–5(–6) months. Certain landraces mature so quickly that they produce grain already 6–8 weeks after planting, long before all other cereals, and provide food early in the growing season. At maturity the stems bend down due to the weight of the grains. Fonio follows the C4 photosynthetic pathway.
Ecology
Fonio is grown at sea level in Gambia, Guinea-Bissau and Sierra Leone, but more often it is cultivated at 600–1500 m altitude. The average temperature in the growing season ranges from 20°C at higher altitudes to 25–30°C near sea level. Fonio is grown in areas with an average annual rainfall of 150–3000 mm, but its cultivation is concentrated in regions with an average annual rainfall of 900–1000 mm. It is not as drought resistant as pearl millet, but fast-maturing landraces are suited to areas with short and unreliable rains. In areas with very low rainfall it is grown in valleys benefiting from run-off water. Fonio can be grown on poor, shallow, sandy or rocky soils unsuitable for other cereals, but does not prosper in saline or heavy soils. On the Fouta Djallon Plateau of Guinea, it grows on acidic soils with very high aluminium contents.
Propagation and planting
Fonio is propagated by seed. The 1000-seed weight is 400–600 mg. Fonio is usually sown at the beginning of the rainy season. Soil preparation is minimal: the fallow vegetation is burnt and the ashes spread, and the soil may be loosened by superficial cultivation. Seed, mixed with an equal quantity of sand or ashes, is usually broadcast, and covered with soil by a light hoeing or brushing with tree branches. The seed rate is 10–30 kg per ha. Fonio is sometimes raised in a nursery and planted out in the field.
Fonio is normally grown as a sole crop, but sometimes intercropped with sorghum or pearl millet. Farmers in Guinea commonly sow various fonio types together and later fill in any gaps with Guinea millet.
Management
Although it has been stated that fonio seldom needs weeding due to its quick establishment and the high seed rates applied, other sources indicate that a weeding at 4–5 weeks after sowing is necessary for good yields. Fonio is usually not fertilized and little is known of its nutrient requirements. In crop rotations fonio often follows rainfed rice, as a short-cycle crop before another crop is sown in the same season. It is also grown at the end of a rotation.
Diseases and pests
Fonio is susceptible to rust (Puccinia oahuensis). Resistance to the nematodes Meloidogyne incognita and Meloidogyne javanica has been recorded in soils where other plant species were infected. Birds can cause serious losses, so bird scaring is usually necessary. Fonio is attacked by parasitic plants of the genus Striga. Fonio seed is not liable to damage by storage pests and stores well.
Harvesting
Fonio is usually cut with a knife or sickle, tied into sheaves, dried and stored under cover. Mechanization is difficult because of lodging. When plants are dry, the grain shatters easily, and therefore it is better to harvest before the dry season has fully established and the relative air humidity has considerably declined. Harvesting is often staggered, to suit the immediate needs of the farmer.
Yield
Grain yields of fonio are normally 600–900 kg/ha, but yields of over 1000 kg/ha have been recorded. In marginal areas yields may be as low as 150–200 kg/ha.
Handling after harvest
Fonio is normally threshed at about 8 days after harvesting, traditionally by beating or trampling. The husks remain on the grains, which therefore retain moisture and must be dried further. The grains are sufficiently dry when they run easily through the fingers. The product after threshing (‘fonio paddy’ or ‘raw fonio’) is further processed in 2 stages: husking (removal of the husks from the grains) and whitening (removal of the fruitwall and the germ). Husking and whitening are done manually and require 4–5 beatings with pestle and mortar, alternated with winnowing. To obtain a product of good quality, all dirt and sand must be removed by repeated washings. The processing cycle is difficult and time-consuming and efforts are being made to develop equipment that will make processing easier. Small-scale fonio processing enterprises can be found in towns, e.g. in Mali and Burkina Faso, aiming at urban and export markets.
Genetic resources
Fonio seems not threatened by genetic erosion. RAPD-analysis has shown a relatively high level of genetic diversity in fonio compared to other millets, possibly due to its outbreeding nature. Most germplasm collections made before 1990 and kept in national genebanks have been lost, but duplicates exist at IRD (Institut de Recherche pour le Développement), Montpellier, France, which keeps more than 400 fonio accessions. Fonio accessions are also conserved in Senegal, Guinea, Mali, Burkina Faso, Togo, Benin and Nigeria. In Nigeria, Benin and Togo germplasm characterization work for a better understanding and utilization of the fonio gene pool has started.
Breeding
So far fonio has been largely neglected in breeding programmes. Breeding efforts are being undertaken in Guinea, but no results are available so far. Improvement of fonio through traditional hybridization does not seem attractive because of insufficient knowledge on its floral biology and the extraordinarily miniature nature of its floral organs.
Prospects
Fonio is wrongly named ‘hungry rice’, because it is not grown to relieve hunger but because of its quality and contribution to food security. It is a crop with a short cycle, able to produce on very poor soils. It is appreciated as a food in West Africa, and its nutritional quality is excellent. Interesting research topics include improved plant architecture to prevent lodging, photoperiod-sensitivity, cultivation techniques, grain size, the development of less laborious processing methods and improvement of farmers’ seed systems. Study of the genetic diversity of fonio and multilocational screening of germplasm are also highly recommended.
Major references
• Burkill, H.M., 1994. The useful plants of West Tropical Africa. 2nd Edition. Volume 2, Families E–I. Royal Botanic Gardens, Kew, Richmond, United Kingdom. 636 pp.
• Froment, D. & Renard, C., 2001. Fonio. In: Raemaekers, R.H. (Editor). Crop production in tropical Africa. DGIC (Directorate General for International Co-operation), Ministry of Foreign Affairs, External Trade and International Co-operation, Brussels, Belgium. pp. 16–22.
• Haq, N. & Dania Ogbe, F., 1995. Fonio (Digitaria exilis and D. iburua). In: Williams, J.T. (Editor). Cereals and pseudocereals. Chapman and Hall, London, United Kingdom. pp. 225–245.
• Hilu, K.W., M’Ribu, K., Liang, H. & Mandelbaum, C., 1997. Fonio millets: ethnobotany, genetic diversity and evolution. South African Journal of Botany 63(4): 185–190.
• National Research Council, 1996. Lost crops of Africa. Volume 1: grains. National Academy Press, Washington D.C., United States. 383 pp.
• Ndoye, M. & Nwasike, C.C., 1993. Fonio millet (Digitaria exilis Stapf) in West Africa. In: Riley, K.W., Gupta, S.C., Seetharam, A. & Mushonga, J.N. (Editors). Advances in small millets. Oxford & IBH Publishing Co., New Delhi, India. pp. 85–94.
• Portères, R., 1976. African cereals: Eleusine, fonio, black fonio, teff, Brachiaria, paspalum, Pennisetum, and African rice. In: Harlan, J.R., de Wet, J.M.J. & Stemler, A.B.L. (Editors). Origins of African plant domestication. Mouton Publishers, The Hague, Netherlands. pp. 409–452.
• van der Hoek, H.N. & Jansen, P.C.M., 1996. Minor cereals. In: Grubben, G.J.H. & Partohardjono, S. (Editors). Plant Resources of SouthEast Asia No 10. Cereals. Backhuys Publishers, Leiden, Netherlands. pp. 150–156.
• Vodouhè, S.R., Zannou, A. & Achigan Dako, E. (Editors), 2003. Actes du premier atelier sur la diversité génétique du fonio (Digitaria exilis Stapf.) en Afrique de l’Ouest. Conakry, Guinée, 4–6 août 1998. IPGRI, Rome, Italy. 73 pp.
• Vodouhè, S.R. & Achigan Dako, E. (Editors), 2003. Renforcement de la contribution du fonio à la sécurité alimentaire et aux revenus des paysans en Afrique de l’Ouest. Actes du séminaire régional sur le fonio, 19–22 Novembre 2001, Bamako, Mali. IPGRI -SSA, Nairobi, Kenya. 71 pp.
Other references
• Busson, F., 1965. Plantes alimentaires de l’ouest Africain: étude botanique, biologique et chimique. Leconte, Marseille, France. 568 pp.
• Clayton, W.D., 1972. Gramineae. In: Hepper, F.N. (Editor). Flora of West Tropical Africa. 2nd Edition. Volume 3, part 2. pp. 277–574.
• Chevalier, A., 1950. Sur l’origine des Digitaria’s cultivés. Revue Internationale de Botanique Appliquée & d’Agriculture Tropicale 30: 329–330.
• Cissé, I.B., 1974–1975. La culture de fonio et quelques aspects écophysiologiques de la plante. Landbouwhogeschool, Wageningen, Netherlands. 72 pp.
• Cruz, J.-F., 2004. Fonio: a small grain with potential. LEISA Magazine 20(1): 16–17.
• de Wet, J.M.J., 1995. Minor cereals. In: Smartt, J. & Simmonds, N.W. (Editors). Evolution of crop plants. 2nd Edition. Longman, London, United Kingdom. pp. 202–208.
• FAO, 1970. Amino-acid content of foods and biological data on proteins. FAO Nutrition Studies No 24, Rome, Italy. 285 pp.
• Hanelt, P. & Institute of Plant Genetics and Crop Plant Research (Editors), 2001. Mansfeld’s encyclopedia of agricultural and horticultural crops (except ornamentals). 1st English edition. Springer Verlag, Berlin, Germany. 3645 pp.
• Harlan, J.R., 1993. Genetic resources in Africa. In: Janick, J. & Simon, J.E. (Editors). New crops. Wiley, New York, United States. p. 65.
• Jideani, I.A., 1990. Acha - Digitaria exilis - the neglected cereal. Agriculture International 42(5): 132–134, 143.
• Jideani, I.A., 1999. Traditional and possible technological uses of Digitaria exilis (acha) and Digitaria iburua (iburu): a review. Plant Foods for Human Nutrition 54: 363–374.
• Konkobo-Yaméogo, C., Chaloub, Y., Kergna, A., Bricas, N., Karimou, R. & Ndiaye, J.-L., 2004. La consommation urbaine d’une céréale traditionnelle en Afrique de l’Ouest: le fonio. Cahiers Agricultures 13(1): 125–128.
• Kuta, D.D., Kwon-Ndung, E.H., Dachi, S., Ukwungwu, M. & Imolehin, E.D., 2003. Potential role of biotechnology tools for genetic improvement of ‘lost crops of Africa’: the case of fonio (Digitaria exilis and Digitaria iburua). African Journal of Biotechnology 2(12): 580–585.
• Kwon-Ndung, E.H., Misari, S.M. & Dachi, S.N., 1998. Collecting germplasm of acha, Digitaria exilis (Kipp.) Stapf, accessions in Nigeria. Plant Genetic Resources Newsletter 116: 30–31.
• Leung, W.-T.W., Busson, F. & Jardin, C., 1968. Food composition table for use in Africa. FAO, Rome, Italy. 306 pp.
• Lewicki, T., 1974. West African food in the Middle Ages: according to Arabic sources. Cambridge University Press, London, United Kingdom. 262 pp.
• Morales-Payán, J.P., Ortiz, J.R., Cicero, J. & Taveras, F., 2002. Digitaria exilis as a crop in the Dominican Republic. In: Janick, J. & Whipkey, A. (Editors). Trends in new crops and new uses. ASHS Press, Alexandria, Virginia, United States. pp. S1–S3.
• Purseglove, J.W., 1972. Tropical crops. Monocotyledons. Volume 1. Longman, London, United Kingdom. 334 pp.
• Sarr, E. & Prot, J.-C., 1985. Pénétration et développement des juvéniles d’une souche de Meloidogyne javanica et d’une race B de M. incognita dans les racines du fonio (Digitaria exilis Stapf). Revue de Nématologie 8: 59–65.
• van der Zon, A.P.M., 1992. Graminées du Cameroun. Volume 2, Flore. Wageningen Agricultural University Papers 92–1. Wageningen Agricultural University, Wageningen, Netherlands. 557 pp.
Sources of illustration
• Henrard, J.Th., 1950. Monograph of the genus Digitaria. Universitaire Pers, Leiden, Netherlands. 999 pp.
• Stapf, O., 1916. Digitaria exilis Stapf. Hooker’s Icones Plantarum 31: t. 3068.
Author(s)
S.R. Vodouhè
IPGRI West and Central Africa, 08 B.P. 0932, Cotonou, Benin
E.G. Achigan Dako
IPGRI West and Central Africa, 08 B.P. 0932, Cotonou, Benin


Editors
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:
Vodouhè, S.R. & Achigan Dako, E.G., 2006. Digitaria exilis (Kippist) Stapf In: Brink, M. & Belay, G. (Editors). PROTA 1: Cereals and pulses/Céréales et légumes secs. [CD-Rom]. PROTA, Wageningen, Netherlands.
 

Traditional healing

Traditional healing

Medicinal trees

Medicinal trees

grain.org - english

Biodiversity Policy & Practice - Daily RSS Feed

Rainforest Portal RSS News Feed

What's New on the Biosafety Protocol

Rainforest Portal RSS News Feed