Ipomoea triloba (three-lobe morning glory)
Index
- Pictures
- Identity
- Taxonomic Tree
- Notes on Taxonomy and Nomenclature
- Description
- Distribution
- Distribution Table
- Risk of Introduction
- Habitat
- Habitat List
- Host Plants and Other Plants Affected
- Biology and Ecology
- Natural enemies
- Notes on Natural Enemies
- Impact
- Uses List
- Detection and Inspection
- Similarities to Other Species/Conditions
- Prevention and Control
- References
- Links to Websites
- Distribution Maps
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Generate reportIdentity
Top of pagePreferred Scientific Name
- Ipomoea triloba L.
Preferred Common Name
- three-lobe morning glory
International Common Names
- English: aiea morning glory; caapi; caapi-doux; little bell; morning glory; wild potato; wild slip
- Spanish: aguialdo rosado; campanilla; campanilla rosado; churristate; pink aguinaldo
Local Common Names
- Cuba: bouiato marrullero
- Germany: dreilappige; trichterwinde
- Japan: hoshiasagao
EPPO code
- IPOTR (Ipomoea triloba)
Taxonomic Tree
Top of page- Domain: Eukaryota
- Kingdom: Plantae
- Phylum: Spermatophyta
- Subphylum: Angiospermae
- Class: Dicotyledonae
- Order: Solanales
- Family: Convolvulaceae
- Genus: Ipomoea
- Species: Ipomoea triloba
Notes on Taxonomy and Nomenclature
Top of pageDescription
Top of pageStems prostrate and twining, usually much branched, 1-3 m long, glabrous or sometimes sparsely pubescent, more densely pubescent on the nodes.
Leaves simple, alternate, petiolate; leaf blades broadly ovate to orbicular, 2-12 cm long and 2-10 cm broad, bases cordate; leaf margins entire, coarsely dentate, or deeply 3-5 lobed.
Inflorescences axillary, with dense several-flowered cymes, occasionally 1-flowered; peduncles 1-10 cm long, stout, angular, glabrous, minutely verruculose toward the apex.
Flowers mostly pink to pale-purple (sometimes white, especially in West Africa (Heine, 1963)), often with darker centre and pale mid-petal areas; pedicel 3-10 mm, firm, angular, thickened at apex, glabrous; sepals 5, free, 6-10 mm long, with 3-5 large, raised central veins, corolla funnel-shaped, 1.8-2 cm long, 1.8-2.5 cm across, glabrous, strongly narrowed at the base, the limb with 5 short, obtuse, mucronulate lobes; stamens 5, attached to the inside of the corolla tube; anthers and filaments white, mostly included, very rarely longer than the corolla tube, filaments densely hairy at base, sparsely covered with curved hairs in lower half; ovary globose, pilose, with a white nectary.
Fruit a subglobose, bristly pubescent, thin-walled capsule, 5-6 mm long and in diameter, 2-celled, 4-valved; seeds usually 4 per capsule, subglobose, 2.5-3.2 mm long, dark-brown.
(After Austin, 1978.)
Distribution
Top of pageThe map is based on published country records: I. triloba specimens have also been collected from Guatemala (R Westbrooks, Animal and Plant Health Inspection Service, USDA, North Carolina, USA, personal communication, 1995), the Lesser Antilles (Adams et al., 1972), Polynesia and Micronesia (Gunn and Ritchie, 1982).
Distribution Table
Top of pageThe 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 2021Continent/Country/Region | Distribution | Last Reported | Origin | First Reported | Invasive | Reference | Notes |
---|---|---|---|---|---|---|---|
Africa |
|||||||
Côte d'Ivoire | Present, Localized | ||||||
Nigeria | Present | ||||||
Senegal | Present, Localized | ||||||
South Africa | Present | ||||||
Asia |
|||||||
Cambodia | Present, Localized | ||||||
China | Present | Present based on regional distribution. | |||||
-Jiangxi | Present | ||||||
India | Present | ||||||
-Gujarat | Present | ||||||
-Karnataka | Present | ||||||
-Kerala | Present | ||||||
-Maharashtra | Present | ||||||
-Rajasthan | Present | ||||||
-Tamil Nadu | Present | ||||||
-Uttar Pradesh | Present | ||||||
-West Bengal | Present | ||||||
Indonesia | Present, Localized | ||||||
-Java | Present | Original citation: van (1965) | |||||
Iran | Present | ||||||
Israel | Present | ||||||
Laos | Present | ||||||
Malaysia | Present | ||||||
-Peninsular Malaysia | Present | ||||||
Myanmar | Present | ||||||
Nepal | Present, Localized | ||||||
Pakistan | Present | ||||||
Philippines | Present, Localized | ||||||
Sri Lanka | Present | Original citation: Dassanayake, 1980 | |||||
Thailand | Present, Localized | ||||||
Turkey | Present, Localized | ||||||
Europe |
|||||||
Spain | Present, Few occurrences | ||||||
North America |
|||||||
Bahamas | Present | Original citation: Adams at al., 1972 | |||||
Belize | Present | ||||||
Cayman Islands | Present | ||||||
Costa Rica | Present, Localized | ||||||
Cuba | Present, Localized | ||||||
Dominica | Present | ||||||
Dominican Republic | Present | ||||||
El Salvador | Present | ||||||
Haiti | Present | ||||||
Honduras | Present, Localized | ||||||
Jamaica | Present, Localized | ||||||
Mexico | Present | ||||||
Nicaragua | Present | ||||||
Panama | Present | ||||||
Puerto Rico | Present, Localized | ||||||
Trinidad and Tobago | Present | ||||||
United States | Present, Widespread | ||||||
-Arizona | Present | ||||||
-Florida | Present | ||||||
-Hawaii | Present | ||||||
Oceania |
|||||||
Australia | Present, Localized | ||||||
Guam | Present | ||||||
Papua New Guinea | Present, Localized | ||||||
South America |
|||||||
Argentina | Present, Localized | ||||||
Bolivia | Present | ||||||
Colombia | Present, Localized | ||||||
Ecuador | Present, Localized | ||||||
Venezuela | Present |
Risk of Introduction
Top of pageHabitat
Top of pageHost Plants and Other Plants Affected
Top of pagePlant name | Family | Context | References |
---|---|---|---|
Citrus | Rutaceae | Main | |
Glycine max (soyabean) | Fabaceae | Other | |
Gossypium (cotton) | Malvaceae | Main | |
Ipomoea batatas (sweet potato) | Convolvulaceae | Other | |
Saccharum officinarum (sugarcane) | Poaceae | Main | |
Sesamum indicum (sesame) | Pedaliaceae | Main | |
Solanum lycopersicum (tomato) | Solanaceae | Main | |
Sorghum bicolor (sorghum) | Poaceae | Main | |
Zea mays (maize) | Poaceae | Main |
Biology and Ecology
Top of pageIn the Philippines, nicking the seed coat with a blade was the most effective dormancy-breaking treatment studied. Sand scarification was effective but damaged the seed. A 40-80% saturation level in the soil favoured germination (Gacutan, 1979).
I. triloba is considered to be an important plant in honey production in Cuba and other Central American countries (Ordetx, 1949).
Natural enemies
Top of pageNatural enemy | Type | Life stages | Specificity | References | Biological control in | Biological control on |
---|---|---|---|---|---|---|
Agrius cingulatus | Herbivore |
Notes on Natural Enemies
Top of pageImpact
Top of pageIn Java, I. triloba is a weed of brushwoods, living fences, sugarcane fields, roadsides, fields and waste places (van Ooststroom, 1965). A nematode assessment survey of the vegetable-growing areas of Barangay Sicsican in Talavera, Neuva, Ecija, Philippines found that I. triloba and several other weeds serve as alternative hosts for root-knot nematodes (Meloidogyne javanica and M. incognita). Such alternative hosts play an important role in the nematodes' ability to survive and persist during the rice season before the vegetable season (Mamari and Alberto, 1989).
In the Philippines, I. triloba is one of the main weeds of monoculture maize (Pamplona, 1988), one of the most common weeds in intercropped maize, sorghum, sunflowers, coconuts, tomatoes, and sesame (Moody, 1986), and has been listed there as one of 21 common weeds of cotton (Paller and Lijauco, 1981).
In one study, varying densities of I. triloba were maintained in monocultures of soyabeans or maize and maize-soyabean intercrops. Weed density did not normally have a significant effect on insect pest populations, but the presence of I. triloba tended to increase damage by insects in soyabeans and to act as a pest attractant in maize (Mercado et al., 1980).
I. triloba was first reported in Israel in 1986 as a weed in cotton (Joel and Liston, 1986).
Studies in the Solomon Islands showed that I. triloba and two other species are alternative hosts for witches' broom disease of sweet potatoes (Jackson and Zettler, 1983).
Detection and Inspection
Top of pageSimilarities to Other Species/Conditions
Top of pageAnother species that is similar to I. triloba is I. x grandifolia. According to Austin (1978), these species may be separated by sepal shape (oblong to narrowly elliptic-oblong for I. triloba versus lanceolate to ovate-lanceolate), sepal length [6-8(10) mm versus 8-11 mm], capsule size (5-6 mm long and in diameter versus 6-7 mm in diameter, capsule pubescence (pilose versus hirsute), and seed size (2.5-3.2 mm long versus 3.5-4 mm long).
I. triloba and I. lacunosa (which is spread in birdseed and millet) may be separated on the basis of flower colour (pink to purple for I. triloba versus white), sepal size [6-8(10) mm long versus (8)11-14 mm long], sepal shape (more or less oblong versus lanceolate), capsule size (5-6 mm long and in diameter versus 10-15 mm in diameter), and seed size (2.5-3.2 mm long versus 5-6 mm long) (Austin, 1978).
I. triloba and a rather common form of the hybrid I. x leucantha (parent species I. lacunosa and I. trichocarpa) may be separated on the basis of sepal shape (more or less oblong for I. triloba versus lanceolate), sepal length [6-8(10) mm versus (8)10-14 mm], capsule size (5-6 mm long and in diameter versus 7-8 mm in diameter), and seed size (2.5-3.2 mm long versus 3.2-4.5 mm long) (Austin, 1978).
Prevention and Control
Top of pageDue 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.
Chemical, Cultural and Sanitary Methods
Coconuts
Research in the Philippines showed that I. triloba was controlled in coconut nurseries with the use of paraquat or by hand weeding at intervals of 1-2 months (Abad and Juan, 1981).
Maize
Field studies to evaluate different herbicides and herbicide combinations in the Philippines showed that pendimethalin alone failed to control I. triloba in maize cv. Pioneer 6181 (Jover et al., 1982). Madrid and Manimtim (1978a) found that atrazine provided good control of broad-leaved weeds, including I. triloba; however, oxyfluorfen provided good control for I. triloba but killed the maize.
Sugarcane and Sorghum
Research by the Hawaiian Sugar Planters' Association indicated that metsulfuron provided good control of I. triloba (Santo, 1989). In another Hawaiian study, conducted during the first 4-6 months of sugarcane growth until the canopy closed, atrazine was found to give excellent control of several broadleaved weeds, including I. triloba (Olney, 1971).
Field trials in sugarcane and sorghum in New South Wales and Queensland (Australia) during 1982-86, showed that I. triloba was moderately susceptible to fluroxypyr, but was controlled with a tank mixture of fluroxypyr and 2,4-D (Webb and Feez, 1987).
Hondrade (1981) found that pendimethalin was ineffective in controlling I. triloba in sugarcane.
In field trials in the Burdekin District of Queensland, 2,4-D and MCPA applied to sugarcane at hilling up gave good control of I. triloba, I. plebeia and I. purpurea, and provided an economical and reliable alternative to aerial spraying. The major Burdekin cane cultivars, Q96 and Q80, could be treated without risk of damage. 2,4-D was the least expensive of the treatments (on the basis of the cost of chemical). Extensive commercial spraying showed that 2,4,5,-T [superseded] could be used to maintain satisfactory weed control, but that higher rates were needed where Cucumis metuliferus or Passiflora subpeltata were also present (Anonymous, 1980).
Mungbeans and Soyabeans
In the Philippines, oxyfluorfen was effective in inhibiting the germination of I. triloba in mungbeans and soyabeans when applied 2 days after planting. Emergence of I. triloba was observed at lower rates, but the seedlings died 2 weeks after treatment (Fabro and Robles, 1982).
In another Philippine study, oxadiazon applied pre-emergence in soyabeans gave excellent control of I. triloba. In another trial, however, oxadiazon controlled I. triloba but severely injured the crop. Combination pre-emergence and post-emergence directed applications of bentazone also provided control (Madrid and Manimtim, 1978b).
Tomatoes and Cabbages
Rice straw, rice hulls and sawdust mulches reduced populations of I. triloba in tomatoes by 50% at 30 days after transplanting. However, the weed eventually penetrated the mulches and grew out of control. In transplanted cabbage, mulching also cut populations of I. triloba in half during the wet season of 1977 in the Philippines (Paller et al., 1979).
Miscellaneous
Pre-emergence application of bromacil was effective in controlling I. triloba in a variety of tropical crops in the Philippines (Mendoza, 1979). In another Philippine study, bentazone applied post-emergence or as a directed spray controlled I. triloba at the 2-3 leaf stage. However, yields were less than with hand weeding and weed control was not season long (Robles et al., 1979).
Biological Control
The phytophagous arthropods (and their natural enemies) in an agroecosystem in the warm region of central Tolima, Colombia were investigated from November 1976 until May 1979. This project found that Agrius cingulatus showed some promise for biological control of I. triloba. On several occasions, this sphingid completely defoliated the weed in soyabean crops without damaging the crop. Larvae placed on soyabean leaves in the laboratory died without feeding (Hallman, 1979).
Regulatory Control
I. triloba is listed as a Federal Noxious Weed in the USA. Introduction is permitted there only by permit from the Animal and Plant Health Inspection Service, USDA.
Preliminary studies indicate that a 0.35% solution of caustic soda (NaOH) in hot water at 92°C is sufficient to kill seeds of I. triloba that contaminate shipments of sesame (caustic soda is used to de-hull or decorticate raw sesame seeds). Preliminary studies also indicate that dry heat (hot air) temperatures of 130°C will kill seeds of I. triloba (R Westbrooks, Animal and Plant Health Inspection Service, USDA, North Carolina, USA, personal communication, 1995).
Regulatory strategies to prevent the world movement and further establishment of exotic pest plants such as I. triloba include foreign prevention (production of weed-free commodities for export to uninfested countries); exclusion (detection and mitigation of weed contaminants in imported products at ports of entry); detection, containments and eradication of incipient infestations, and cost-effective control of widespread species (Westbrooks, 1991).
References
Top of page1980. An alternative to aerial spraying. Cane Growers' Quarterly Bulletin, 43(4):107
Abad R; Juan N, 1981. Effect of different rates of glyphosate followed by paraquat on the weed population in coconut (Cocos nucifera L.). Philippine Journal of Weed Science, 8:5-14.
Adams C; Proctor G; Read R, 1972. Flowering plants of Jamaica. Mona, Jamaica: University of the West Indies.
Auld B; Medd R, 1992. Weeds. An illustrated botanical guide to the weeds of Australia. Melbourne, Australia: Inkata Press.
Austin D, 1978. The Ipomoea batatas complex - I. Taxonomy. Bulletin of the Torrey Botanical Club, 105(2):114-129.
Dassanayake M; ed, 1980. A Revised Handbook to the Flora of Ceylon. Volume I. New Dehli, India: Amerind Publishing Co.
EPPO, 2014. PQR database. Paris, France: European and Mediterranean Plant Protection Organization. http://www.eppo.int/DATABASES/pqr/pqr.htm
Gunn C; Ritchie C, 1982. The 1982 report of the Technical Committee to Evaluate Noxious Weeds. Evaluation of taxa proposed for listing as Federal Noxious Weeds. Riverdale, Maryland, USA: US Department of Agriculture, Animal and Plant Health Inspection Service, Plant Protection and Quarantine.
Haselwood E; Motter G; eds, 1966. Handbook of Hawaiian Weeds. Hawaii: Experiment Station of the Hawaiian Sugar Planters' Association.
Heine H, 1963. Convolvulaceae. In: Hepper FN, ed. Flora of West Tropical Africa, Vol 2, 2nd edition. London, UK: Crown Agents, 335-352.
Hondrade E, 1981. Evaluation of some pre-emergence herbicides for weed control in sugarcane. SMARC Monitor, 2(4):10.
Joel DM; Liston A, 1986. New adventive weeds in Israel. Israel Journal of Botany, 35(3-4):215-223
Kearney T; Peebles R, 1951. Arizona Flora. Berkeley and Los Angeles, USA: University of California Press.
Madrid M Jr; Manimtim M, 1978a. Weed control in corn. Weed Science Report, 1976-77. Los Banos, Philippines: University of the Philippines at Los Banos (College of Agriculture, Department of Agronomy), 37-42.
Mamari E; Alberto R, 1989. Root knot nematodes infecting some common weeds in vegetable growing areas of Sicsican. International Nematology Network Newsletter, 6:37-39.
Olney V, 1971. Development of weed control in Hawaiian sugarcane fields. Third Conference of the Asian-Pacific Weed Science Society, Kuala Lumpur, Malaysia: Asian Pacific Weed ScienceSociety, 35:1-6.
Ordetx G, 1949. The Aguinaldos, major bee plants of Cuba. American Bee Journal, 89:72-73.
Robles R; Fabro L; Nunez Z, 1979. Weed control in legumes (dry season, 1978). Weed Science Report, 1977-78. Los Banos, Philippines: University of the Philippines at Los Banos (College of Agriculture, Department of Agronomy), 46-54.
Santo L, 1989. Weed control with cultural and chemical methods in Hawaiian sugarcane. Proceedings of the Western Society of Weed Science, 42:78-82.
van Ooststroom S, 1965. Ipomoea. In: Backer CA, Bakhuizen van den Brink RC Jr, eds. Flora of Java, Vol. 2. Groningen, The Netherlands: Noordhoff, 490-496.
Westbrooks R, 1989. Regulatory exclusion of Federal Noxious Weeds from the United States. Ph.D. Dissertation. Raleigh, North Carolina: Department of Botany, North Carolina State University.
Westbrooks R; Eplee R, 1989. Federal Noxious Weeds in Florida. Proceedings of the Southern Weed Science Society, 42:316-321.
Westbrooks R; Eplee R, 1992. Annual Report. Whiteville Plant Methods Center. Whiteville, North Carolina, USA: U.S. Department of Agriculture, Animal and Plant Health Inspection Service, Plant Protection and Quarantine.
Distribution References
Adams C, Proctor G, Read R, 1972. Flowering plants of Jamaica., Mona, Jamaica: University of the West Indies.
Auld B, Medd R, 1992. Weeds. An illustrated botanical guide to the weeds of Australia., Melbourne, Australia: Inkata Press.
CABI, Undated. Compendium record. Wallingford, UK: CABI
CABI, Undated a. CABI Compendium: Status inferred from regional distribution. Wallingford, UK: CABI
CABI, Undated b. CABI Compendium: Status as determined by CABI editor. Wallingford, UK: CABI
Gunn C, Ritchie C, 1982. The 1982 report of the Technical Committee to Evaluate Noxious Weeds. Evaluation of taxa proposed for listing as Federal Noxious Weeds., Riverdale, Maryland, USA: US Department of Agriculture, Animal and Plant Health Inspection Service, Plant Protection and Quarantine.
Ordetx G, 1949. The Aguinaldos, major bee plants of Cuba. American Bee Journal. 72-73.
Westbrooks R, Eplee R, 1989. Federal Noxious Weeds in Florida. [Proceedings of the Southern Weed Science Society], 42 316-321.
Links to Websites
Top of pageWebsite | URL | Comment |
---|---|---|
GISD/IASPMR: Invasive Alien Species Pathway Management Resource and DAISIE European Invasive Alien Species Gateway | https://doi.org/10.5061/dryad.m93f6 | Data source for updated system data added to species habitat list. |
Distribution Maps
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