Oryza longistaminata (perennial wild rice)
- Taxonomic Tree
- Notes on Taxonomy and Nomenclature
- Distribution Table
- Risk of Introduction
- Hosts/Species Affected
- Host Plants and Other Plants Affected
- Biology and Ecology
- Notes on Natural Enemies
- Uses List
- Similarities to Other Species/Conditions
- Prevention and Control
- Links to Websites
- Distribution Maps
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PicturesTop of page
IdentityTop of page
Preferred Scientific Name
- Oryza longistaminata A. Chev. & Roehr. 1914
Preferred Common Name
- perennial wild rice
Other Scientific Names
- Oryza barthii sensu Hutch. & Dalz. 1836, non A. Chev.
- Oryza dewildemanii Vanderyst 1920
- Oryza perennis Wild 1965
- Oryza sylvestris A. Chev. 1911
International Common Names
- English: rhizomatous wild rice
- French: diga; riz sauvage; riz sauvage à rhizomes
Local Common Names
- Germany: Reis, Wilder
- ORYBA (Oryza barthii)
- ORYLO (Oryza longistaminata)
Taxonomic TreeTop of page
- Domain: Eukaryota
- Kingdom: Plantae
- Phylum: Spermatophyta
- Subphylum: Angiospermae
- Class: Monocotyledonae
- Order: Cyperales
- Family: Poaceae
- Genus: Oryza
- Species: Oryza longistaminata
Notes on Taxonomy and NomenclatureTop of page
DescriptionTop of page
Leaf sheaths are pale-green to brownish, glabrous, nearly as long as the internodes, with 15 mm long auricles at the junction with the blade. The triangular ligule is often split down the middle, 0.8-5.5 cm long with an acute tip. Leaf blades are bright to dark green,10-75 cm long, 0.5-2.5 cm wide, are broadest below the middle, rough along the margins, otherwise smooth, glabrous with an indistinct mid-rib.
The panicle is 16-40 cm long, erect or slightly drooping with a tuft of hairs at the base of branches. Narrowly oblong spikelets, on 0.5-4 mm long pedicels, are 7-15 mm long, scabrid to hispid and shed when mature. Glumes are reduced to a narrow membranous rim. Sterile lemmas are 2-3.8 mm long, glabrous and smooth. Fertile lemmas are slightly shorter than the spikelet, stiffly hispid, with 6 stamens, a blackish stigma and awns 2.6-7.5 cm, usually pink or purplish when fresh. The seeds are 7.5-8.5 mm long, oblong, glabrous, light-brown and glossy.
DistributionTop of page
Distribution TableTop of page
The distribution in this summary table is based on all the information available. When several references are cited, they may give conflicting information on the status. Further details may be available for individual references in the Distribution Table Details section which can be selected by going to Generate Report.Last updated: 25 Feb 2021
|Continent/Country/Region||Distribution||Last Reported||Origin||First Reported||Invasive||Reference||Notes|
|Congo, Democratic Republic of the||Present|
Risk of IntroductionTop of page
HabitatTop of page
Hosts/Species AffectedTop of page
Host Plants and Other Plants AffectedTop of page
|Oryza sativa (rice)||Poaceae||Main|
Biology and EcologyTop of page
Notes on Natural EnemiesTop of page
ImpactTop of page
Although seed is shed at maturity, some wild rice seed may contaminate commercial rice grain (Parker and Dean, 1976), reducing its quality, as additional polishing may be required to remove the red pericarp of wild rice grains.
As well as the competitive effect on the crop, both O. longistaminata and O. barthii are alternative hosts of some important rice pests and pathogens including rice yellow mottle sobemovirus (John et al., 1984) and rice bacterial blight (Xanthomonas oryzae pv. oryzae) (Buddenhagen, 1982).
UsesTop of page
Uses ListTop of page
Animal feed, fodder, forage
- Related to
Human food and beverage
Similarities to Other Species/ConditionsTop of page
Another African wild rice, O. punctata, is also distinguished from O. longistaminata by the absence of rhizomes. It is synonymous with O. schweinfurthiana, O. sativa var. punctata and O. eichingeri var. longistaminata, and is known from Angola, Côte d'Ivoire, Ghana, Kenya, Madagascar, Nigeria, Sudan, Swaziland, Tanzania, Uganda, Zanzibar and is also present in Thailand (Clayton, 1970; Fernandes et al., 1971; Hepper, 1972).
The annual O. punctata is distinguished from O. barthii by its small seeds <5 mm long). The spikelets of O. punctata are up to 6.2 mm long and they are approximately 2.5 times as long as they are wide. In O. barthii, the spikelets are somewhat larger (7-11 mm long). The seeds of both these wild rices are shed at maturity, unlike those of the cultivated forms O. glaberrima and O. sativa.
Red rice, weedy, shattering forms of O. sativa with a red pericarp or occasionally with black seeds have on rare occasions been introduced with planting seed into Africa, for example in Swaziland (Parker and Dean, 1976). These are sometimes referred to as O. rufipogon, although this is strictly a perennial species. The 'red rices' cause serious weed problems in the Americas (Holm et al., 1997). They lack rhizomes, but in common with O. longistaminata have very long ligules (1.25-3.0 cm) on lower leaves. In comparison, those of O. barthii and O. punctata are less than 10 mm long.
Prevention and ControlTop of page
Due to the variable regulations around (de)registration of pesticides, your national list of registered pesticides or relevant authority should be consulted to determine which products are legally allowed for use in your country when considering chemical control. Pesticides should always be used in a lawful manner, consistent with the product's label.Cultural Control
As the wild rices do not germinate in the absence of adequate oxygen, they are only weed problems if they are allowed to germinate and establish in drained soil prior to flooding or in the case of O. longistaminata, when the weed regenerates from rhizomes. The annual species' are therefore not serious weeds of transplanted rice, provided clean seed is used and adequate water control is employed (Parker and Dean, 1976). Seedlings of the rice crop and wild rices are morphologically similar. Planting the crop in rows can therefore help to identify any wild rice plants developing in the inter-rows. In India, purple-leaved rice cultivars were developed so that crop and weedy rices could be readily distinguished to facilitate hand weeding (Malik and Moorthy, 1996). Use of a short-term rice cultivar, which matures before the wild rice plants have begun to shed seed, results in more contamination of the harvested grain, but reduces the long term problem by breaking the cycle of introduction of new weed seed into the soil (Parker and Dean, 1976).
A traditional control measure for O. longistaminata, practised in Mali, has been the rotational 'underwater' mowing of plants on fallow areas of the Niger floodplain (Nyoka, 1983). This provides adequate suppression of the weed to allow production of a rice crop in the subsequent rainy season although the technique is very labour intensive. The rhizome system of O. longistaminata is relatively shallow, so only shallow tillage is needed to sever it from adventitious roots. Repeated dry-season tillage can therefore lead to the desiccation and death of the rhizome system. Timing in relation to soil moisture can be critical. Although a single ploughing prior to flooding failed to control the weed in trials conducted in Mali (WARDA, 1979), 'undercutting' with a blade set shallowly in the soil was effective if carried out twice prior to planting. Tillage has also been shown to influence O. barthii populations (Davies, 1983). A stale seedbed technique using rotary cultivations was shown to be particularly effective, leading to reduced levels of infestation and increased rice yields in Senegal.
The herbicide dalapon has given satisfactory control of both O. longistaminata and O. barthii on fallow land (Boeken, 1972). Pre-sowing applications of glyphosate or use of the herbicide on fallow land provide effective control of both species (Aubin et al., 1974; Diarra, 1978; Davies, 1983).
ReferencesTop of page
Armstrong K, 1968. Weed control on a Swaziland rice and sugar-cane estate. Proceedings of the 9th Weed Control Conference, 9:687-693.
Aubin JP; Deuse J; Guilloux P; Reynard A, 1975. A contribution to the study of glyphosate, a systemic herbicide for control of rhizomatous wild rice (Oryza longistaminata) in irrigated rice crops in the valley and delta of the Senegal river. 2éme Symposium sur le Desherbage des Cultures Tropicales, organized by COLUMA. Paris, France: Comité Frantaise de Lutte contre les Mauvaises Herbes, 93-103.
Clayton WD, 1970. Gramineae (Part 1). In: Milne-Redhead E, Polhill RM, eds. Flora of Tropical East Africa. London, UK: Crown Agents for Oversea Governments and Administrations.
Fernandes A; Laurnet E; Wild H, 1971. Flora Zambesiaca, Volume 10, Part 1. London, UK: Crown Agents.
Hepper FN, 1972. Flora of West Tropical Africa, Volume 3, Part 2. London, UK: Crown Agents.
Holm LG; Doll J; Holm E; Pancho JV; Herberger JP, 1997. World Weeds: Natural Histories and Distribution. New York, USA: John Wiley & Sons Inc.
IER, 1989. Internal Report: Commission technique specialisee de productions vivrieres et oleagineuses, Malherbologie campagne 1988-89. Bamako, Mali: Institut d'Economie Rurale.
Katayama T, 1969. Botanical studies in the genus Oryza. Part II. Germination Behavior. Memoirs of the Faculty of Agriculture. Kagoshima University, 7:89-119.
Khush GS, 1997. Origin, dispersal, cultivation and variation of rice. Plant Molecular Biology, 35:25-34.
Liberia; West Africa Rice Development Association, 1979. Annual research report May 1979. Annual research report May 1979. West Africa Rice Development Association. Monrovia Liberia, Vol. 3 Special Research Projects:201 pp.
Maijisu B, 1970. A potentially dangerous weed of rice in East Africa. East African Agriculture and Forestry Research Organisation Newsletter. Nairobi, Kenya: EAAFRON.
Malik RK; Moorthy BTS, 1996. Present status and management of weeds in rice in south Asia. In: Auld BA, Kim KU, eds. Weed Management in Rice. Plant Production and Protection Paper 139. Rome, Italy: FAO, 125-139.
Nyoka GC, 1983. Weed problems and control practices in deepwater and floating rice in Mali. In: Deat M, Marnotte P, eds. Proceedings of the Second Biannual Conference. Abidjan, Côte d'Ivoire: West African Weed Science Society, 146-157.
Thottapilly G; Rossel HW, 1993. Evaluation of resistance to rice yellow mottle virus in Oryza species. Indian Journal of Virology, 9(1):65-73.
Tropicos, 1998. Nomenclatural Data Base. Missouri Botanical Garden. World Wide Web page at http://ginko.motbot.org.
Vales M, 1985. Study of complete resistance to Pyricularia oryzae of Oryza sativa
Zhang Q; Wang CL; Shi AN; Bai JF; Ling SC; Li DY; Chen CB; Pang HH, 1994. Genetic studies on resistance to bacterial blight (Xanthomonas oryzae pv. oryzae in nine rice cultivars. Scientia Agricultura Sinica, 27(5):1-9.
Afolabi O, Amoussa R, Bilé M, Oludare A, Gbogbo V, Poulin L, Koebnik R, Szurek B, Silué D, 2016. First report of bacterial leaf blight of rice caused by Xanthomonas oryzae pv. oryzae in Benin. Plant Disease. 100 (2), 515. http://apsjournals.apsnet.org/loi/pdis DOI:10.1094/PDIS-07-15-0821-PDN
Anon, 1971. Flora Zambesiaca., 10 (1) [ed. by Fernandes A, Laurent E, Wild H]. London, UK: Crown Agents.
Clayton WD, 1970. Gramineae (Part 1). In: Flora of Tropical East Africa, [ed. by Milne-Redhead E, Polhill RM]. London, UK: Crown Agents for Oversea Governments and Administrations.
Hepper FN, 1972. Flora of West Tropical Africa., 3 (2) London, UK: Crown Agents.
Tropicos, 1998. Nomenclatural Data Base., Missouri Botanical Garden. http://ginko.motbot.org
Wonni I, Ouedraogo L, Verdier V, 2011. First report of bacterial leaf streak caused by Xanthomonas oryzae pv. oryzicola on rice in Burkina Faso. Plant Disease. 95 (1), 72-73. http://apsjournals.apsnet.org/loi/pdis DOI:10.1094/PDIS-08-10-0566
Distribution MapsTop of page
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