Solanum seaforthianum (Brazilian nightshade)
Index
- Pictures
- Identity
- Summary of Invasiveness
- Taxonomic Tree
- Notes on Taxonomy and Nomenclature
- Description
- Plant Type
- Distribution
- Distribution Table
- History of Introduction and Spread
- Risk of Introduction
- Habitat
- Habitat List
- Hosts/Species Affected
- Biology and Ecology
- Climate
- Air Temperature
- Rainfall
- Soil Tolerances
- Notes on Natural Enemies
- Means of Movement and Dispersal
- Pathway Causes
- Pathway Vectors
- Impact Summary
- Environmental Impact
- Risk and Impact Factors
- Uses
- Uses List
- Prevention and Control
- References
- Links to Websites
- Contributors
- Distribution Maps
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Top of pageIdentity
Top of pagePreferred Scientific Name
- Solanum seaforthianum Andrews
Preferred Common Name
- Brazilian nightshade
Other Scientific Names
- Solanum cyrrhosum Dunal
- Solanum kerrii Bonati
- Solanum prunifolium Roem. & Schult.
- Solanum salignum Roem. & Schult.
- Solanum seaforthianum var. disjunctum O.E. Schulz
- Solanum venustum Kunth
International Common Names
- English: Italian jasmine; potato creeper; potato-creeper; St Vincent's lilac; St. Vincent lilac; star potato vine
- Spanish: guindilla; jazmín de Italia; josefina (Mexico); tomatillo
- French: liane pomme de terre; liane pomme Édouard; petite liane patate
Local Common Names
- Chinese: nan qing qi
- Australia: blue potato vine; climbing nightshade; vining solanum
- Cuba: jazmín de Italia
- Dominican Republic: jazmín italiano; lila
- Mexico: guindilla; piocha
- Netherlands: seaforth's nachtshade
- Puerto Rico: falsa belladona
- South Africa: aartappelranker (Afrikaans); climbing nightshade; ijalamu (isiZulu)
EPPO code
- SOLSE (Solanum seaforthianum)
Summary of Invasiveness
Top of pageS. seaforthianum is a very aggressive woody vine with the capacity to invade natural forests, natural grasslands, forest margins, urban bushland, riverbanks, crops, pastures, roadsides, disturbed sites, and waste areas (ISSG, 2008; PIER, 2014, USDA-ARS, 2014). Plants of S. seaforthianum produce hundreds of small seeds which can be easily dispersed by birds, cattle, and by watercourses (Gallagher et al., 2010; Queensland Department of Primary Industries and Fisheries, 2011; BioNET-EAFRINET, 2014). Once established, S. seaforthianum is able to grow forming dense monocultures that overtop and smother native plant species. S. seaforthianum is included in the Global Compendium of Weeds (Randall, 2012) and is also listed as an invasive plant and/or noxious weed in China, India, Taiwan, Namibia, South Africa, Cuba, Puerto Rico and several islands in the Pacific Ocean including Hawaii, French Polynesia, and New Caledonia.
Taxonomic Tree
Top of page- Domain: Eukaryota
- Kingdom: Plantae
- Phylum: Spermatophyta
- Subphylum: Angiospermae
- Class: Dicotyledonae
- Order: Solanales
- Family: Solanaceae
- Genus: Solanum
- Species: Solanum seaforthianum
Notes on Taxonomy and Nomenclature
Top of page
The family Solanaceae includes about 102 genera and 2460 species (Stevens, 2012). Members of this family are characterized by solitary or clustered flowers with sepals and petals, five in number and fused; five stamens; and a superior ovary composed of two fused carpels. Flowers are usually conspicuous and are pollinated mainly by insects (Stevens, 2012). Many of the Solanaceae species evolved in the Andean and Amazonian regions of South America in habitats that vary dramatically including rainforests that receive more than 3000 mm of precipitation annually, deserts with virtually no rainfall, and high mountains with regular snowfall and subfreezing temperatures (Bombarely et al., 2011).
The genus Solanum contains almost half of all the species within this family (ca. 1250-1700 species) and many formerly independent genera like Lycopersicon or Cyphomandra are now included in Solanum as subgenera or sections (Weese and Bohs, 2007; Stevens, 2012). The Solanaceae is commonly known as “the nightshade family” due to the poisonous alkaloids present in some species (Weese and Bohs, 2007). S. seaforthianum takes its species epithet from Lord Seaforth (Francis Mackenzie Humberston, 1754-1815), governor of Barbados from 1801 to 1806.
Description
Top of pageWoody vines, twining by the petioles. Stems terete, glabrous or sparsely pubescent. Leaves simple or more often pinnatifid or pinnately lobed with up to 4 pairs of leaflets, (2-) 3.5-10(-13) x (1-)2-9(-11) cm, elliptic to broadly triangular in outline, widest in the basal third, membranous, the upper surfaces glabrous or with tiny simple uniseriate trichomes on the veins and margins, the lower surfaces glabrous; base acute, truncate or slightly cordate, occasionally oblique and asymmetric; margins less commonly entire, usually 3-7 lobed, the lobes to 5 x 2 cm, smaller basiscopically; apex acute to acuminate; petioles 1-4 cm long. Inflorescences terminal, later lateral, to 25 or more cm long, with many open, divaricate branches, with up to 100 or more flowers, glabrous; pedicels 0.8-1.4 cm, Flowers all perfect, 5-merous. Buds globose, slightly inflated, the corolla strongly exserted from the calyx tube long before anthesis. Calyx tube approximately 0.5 mm, flattened and open, the lobes < 0.2 mm long, Corolla 1.1-2.5 cm in diameter, violet or pale violet, stellate-rotate, lobed ½ to 2/3 of the way to the base, the lobes 5-9 x 3-4.5 mm, spreading or slightly cupped at anthesis, densely and minutely pubescent on the tips and margins; free portion of filaments markedly unequal, the longest filament 2-3 mm, glabrous; anthers 2-3 x 1-1.5 mm, occasionally one anther slightly larger, ellipsoid, loosely connivent, yellow, poricidal ;ovary glabrous; style 7-10 mm long, stigma capitate, minutely papillose. Fruit a globose berry, 0.8-1.4 cm in diameter, bright shiny red when ripe, glabrous, the pericarp thin; Seeds 4-20 per berry, 4-4.5 x 2.5-3 mm, flattened-reniform, pale yellowish tan, the surfaces minutely pitted (Knapp, 2010).
Distribution
Top of pageThe native distribution range of S. seaforthianum is uncertain. It has been suggested that it is probably native to dry forests and thorn scrub of islands in the West Indies and coastal northern South America in Colombia and Venezuela (Wagner et al., 1999; Nee, 1999; Knapp, 2010). However, other authors believe that the species has a broader native distribution range and they suggest that S. seaforthianum is probably native to south-eastern USA (i.e., Florida), Mexico, Central America, the West Indies, and Venezuela and Colombia in tropical South America (ISSG, 2008; Gallagher et al., 2010; USDA-ARS, 2014; USDA-NRCS, 2014). Until additional data is presented to clarify the distribution range of the species, this datasheet follows the most conservative distribution and reports S. seaforthianum as native to Trinidad and Tobago, Colombia and Venezuela and as introduced elsewhere (see distribution table for details).
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: 10 Feb 2022Continent/Country/Region | Distribution | Last Reported | Origin | First Reported | Invasive | Reference | Notes |
---|---|---|---|---|---|---|---|
Africa |
|||||||
Botswana | Present | Introduced | |||||
Burundi | Present | Introduced | |||||
Congo, Democratic Republic of the | Present | Introduced | |||||
Ethiopia | Present | Introduced | |||||
Kenya | Present | Introduced | Invasive | ||||
Malawi | Present | Introduced | |||||
Mauritius | Present | Introduced | |||||
Mayotte | Present | Introduced | Invasive | ||||
Mozambique | Present | Introduced | |||||
Namibia | Present | Introduced | Invasive | ||||
Réunion | Present | Introduced | Invasive | ||||
Rwanda | Present | Introduced | |||||
South Africa | Present | Introduced | Invasive | Eastern Cape, KwaZulu-Natal, Mpumalanga, Gauteng and Limpopo | |||
Tanzania | Present | Introduced | |||||
Uganda | Present | Introduced | Invasive | ||||
Zambia | Present | Introduced | |||||
Zimbabwe | Present | Introduced | 1918 | Invasive | |||
Asia |
|||||||
China | Present | Present based on regional distribution. | |||||
-Yunnan | Present | Introduced | Invasive | ||||
India | Present | Present based on regional distribution. | |||||
-Andhra Pradesh | Present | Introduced | Invasive | ||||
-Assam | Present | Introduced | Invasive | ||||
-Himachal Pradesh | Present | Introduced | Invasive | ||||
-Jammu and Kashmir | Present | Introduced | Invasive | ||||
-Manipur | Present | Introduced | Invasive | ||||
-Meghalaya | Present | Introduced | Invasive | ||||
-Mizoram | Present | Introduced | Invasive | ||||
-Nagaland | Present | Introduced | Invasive | ||||
-Sikkim | Present | Introduced | Invasive | ||||
-Tripura | Present | Introduced | Invasive | ||||
-Uttarakhand | Present | Introduced | Invasive | ||||
-West Bengal | Present | Introduced | Invasive | ||||
Japan | Present | ||||||
Taiwan | Present | Introduced | Invasive | ||||
Europe |
|||||||
Italy | Present | ||||||
North America |
|||||||
Barbados | Present | Introduced | Widespread | ||||
Belize | Present | Introduced | |||||
Costa Rica | Present | Introduced | |||||
Cuba | Present | Introduced | Invasive | ||||
Dominica | Present | Introduced | Widespread | ||||
Dominican Republic | Present | Introduced | |||||
El Salvador | Present | Introduced | |||||
Guadeloupe | Present | Introduced | Widespread | ||||
Guatemala | Present | Introduced | |||||
Honduras | Present | Introduced | |||||
Martinique | Present | Introduced | Widespread | ||||
Mexico | Present | Introduced | Veracruz, Chiapas, Oaxaca, Tabasco, Yucatán | ||||
Montserrat | Present | Introduced | Widespread | ||||
Netherlands Antilles | Present, Widespread | Introduced | |||||
Nicaragua | Present | Introduced | |||||
Panama | Present | Introduced | |||||
Puerto Rico | Present | Introduced | Invasive | Naturalized. Also in Vieques Is | |||
Saint Lucia | Present | Introduced | Widespread | ||||
Saint Vincent and the Grenadines | Present | Introduced | Widespread | ||||
Trinidad and Tobago | Present | Native | |||||
U.S. Virgin Islands | Present | Introduced | Invasive | St. Croix, St. Thomas | |||
United States | Present | Present based on regional distribution. | |||||
-Florida | Present | Introduced | |||||
-Hawaii | Present | Introduced | Invasive | ||||
Oceania |
|||||||
Australia | Present | Present based on regional distribution. | |||||
-New South Wales | Present | Introduced | Invasive | ||||
-Queensland | Present | Introduced | Invasive | ||||
-South Australia | Present | Introduced | Invasive | ||||
-Western Australia | Present | Introduced | Invasive | ||||
French Polynesia | Present | Introduced | Invasive | ||||
New Caledonia | Present | Introduced | Invasive | ||||
Papua New Guinea | Present | Introduced | Invasive | ||||
Vanuatu | Present | Introduced | |||||
South America |
|||||||
Brazil | Present | Introduced | Cultivated | ||||
Colombia | Present | Native | |||||
French Guiana | Present | ||||||
Peru | Present | ||||||
Venezuela | Present | Native |
History of Introduction and Spread
Top of pageDetermining the date of introduction of S. seaforthianum is very difficult, mainly because the native distribution range of this species remains unclear and it has been widely cultivated as an ornamental in many tropical and subtropical regions of the world. For example, in the nineteenth century S. seaforthianum was cultivated in England from material introduced from the West Indies by Lord Seaforth (Francis Mackenzie Humberston, 1754-1815), governor of Barbados from 1801 to 1806 (Howard, 1979). S. seaforthianum was also reported as a “cultivated plant” on St Croix Island in 1879 (Eggers, 1879) and in gardens in Puerto Rico in 1881 (Bello Espinosa, 1881). By the start of the twentieth century, it was listed as cultivated and naturalized in Cuba, Jamaica, Hispaniola, St Thomas, St Croix, Guadeloupe, Dominica, Martinique, St Vincent, and Barbados (Urban, 1905). The paucity of collections and the relatively late dates of specimens of this species in the US National Herbarium from the West Indies, suggest that this species was introduced there rather than native.
Risk of Introduction
Top of pageThe risk of introduction of S. seaforthianum is high. This species is an aggressive invasive vine that has been widely cultivated as an ornamental. In addition, S. seaforthianum plants produce large numbers of seeds which can be easily dispersed by birds, cattle, and watercourses.
Habitat
Top of pageS. seaforthianum is an ornamental vine cultivated in both tropical and subtropical climates in elevations ranging from sea levels to 1300 -1500 metres (MacKee, 1994; Flora of China Editorial Committee, 2014). Once naturalized, the species can be found growing in natural forests, natural grasslands, forest margins, urban bushland, riverbanks, crops, orchards, pastures, roadsides, disturbed sites, and waste areas in both dry and wet environments (Acevedo-Rodríguez, 2005; ISSG, 2008; Queensland Department of Primary Industries and Fisheries, 2011; PIER, 2014, USDA-ARS, 2014).
Habitat List
Top of pageCategory | Sub-Category | Habitat | Presence | Status |
---|---|---|---|---|
Terrestrial | Managed | Managed grasslands (grazing systems) | Present, no further details | Harmful (pest or invasive) |
Terrestrial | Managed | Managed grasslands (grazing systems) | Present, no further details | Natural |
Terrestrial | Managed | Managed grasslands (grazing systems) | Present, no further details | Productive/non-natural |
Terrestrial | Managed | Disturbed areas | Present, no further details | Natural |
Terrestrial | Managed | Disturbed areas | Present, no further details | Productive/non-natural |
Terrestrial | Managed | Rail / roadsides | Present, no further details | Natural |
Terrestrial | Managed | Rail / roadsides | Present, no further details | Productive/non-natural |
Terrestrial | Managed | Urban / peri-urban areas | Present, no further details | Natural |
Terrestrial | Managed | Urban / peri-urban areas | Present, no further details | Productive/non-natural |
Terrestrial | Natural / Semi-natural | Natural forests | Present, no further details | Harmful (pest or invasive) |
Terrestrial | Natural / Semi-natural | Natural forests | Present, no further details | Natural |
Terrestrial | Natural / Semi-natural | Natural forests | Present, no further details | Productive/non-natural |
Terrestrial | Natural / Semi-natural | Natural grasslands | Present, no further details | Harmful (pest or invasive) |
Terrestrial | Natural / Semi-natural | Natural grasslands | Present, no further details | Natural |
Terrestrial | Natural / Semi-natural | Natural grasslands | Present, no further details | Productive/non-natural |
Terrestrial | Natural / Semi-natural | Riverbanks | Present, no further details | Harmful (pest or invasive) |
Terrestrial | Natural / Semi-natural | Riverbanks | Present, no further details | Natural |
Terrestrial | Natural / Semi-natural | Riverbanks | Present, no further details | Productive/non-natural |
Terrestrial | Natural / Semi-natural | Scrub / shrublands | Present, no further details | Harmful (pest or invasive) |
Terrestrial | Natural / Semi-natural | Scrub / shrublands | Present, no further details | Natural |
Terrestrial | Natural / Semi-natural | Scrub / shrublands | Present, no further details | Productive/non-natural |
Hosts/Species Affected
Top of pageS. seaforthianum is listed as a common weed in groves, hedgerows, and waste areas in many tropical fruit orchards (i.e., lime, avocado, and mango groves) in South Florida (Crane et al., 2008).
Biology and Ecology
Top of pageGenetics
The chromosome number reported for S. seaforthianum is n = 12 (Sarkar et al., 1980).
Reproductive Biology
All Solanum species have poricidally dehiscent anthers that make this genus an example of the buzz pollination syndrome. This pollination syndrome can be found in about 200 genera of flowering plants (Buchmann, 1983). Solanum flowers are mainly hermaphroditic, nectar is absent and pollen is the exclusive floral reward. Pollination in these flowers is performed by insects (mainly bees). The species S. seaforthianum is reported by Wagner et al. (1999) as self-compatible.
Physiology and Phenology
In Puerto Rico and the Virgin Islands, S. seaforthianum has been reported flowering almost throughout the year, and fruits have been collected in January, February, and June (Acevedo-Rodríguez, 2005).
Environmental Requirements
S. seaforthianum grows best on well drained soils with high organic matter content and pH ranging from 5.6 to 6.5 in sunny areas with temperatures ranging from 20°C to 35°C. It does not tolerate water-logging and frost conditions during extended periods (PROTA, 2014).
Climate
Top of pageClimate | Status | Description | Remark |
---|---|---|---|
Af - Tropical rainforest climate | Tolerated | > 60mm precipitation per month | |
Am - Tropical monsoon climate | Preferred | Tropical monsoon climate ( < 60mm precipitation driest month but > (100 - [total annual precipitation(mm}/25])) | |
As - Tropical savanna climate with dry summer | Preferred | < 60mm precipitation driest month (in summer) and < (100 - [total annual precipitation{mm}/25]) | |
Aw - Tropical wet and dry savanna climate | Preferred | < 60mm precipitation driest month (in winter) and < (100 - [total annual precipitation{mm}/25]) | |
BS - Steppe climate | Tolerated | > 430mm and < 860mm annual precipitation | |
Cs - Warm temperate climate with dry summer | Tolerated | Warm average temp. > 10°C, Cold average temp. > 0°C, dry summers | |
Cw - Warm temperate climate with dry winter | Tolerated | Warm temperate climate with dry winter (Warm average temp. > 10°C, Cold average temp. > 0°C, dry winters) |
Air Temperature
Top of pageParameter | Lower limit | Upper limit |
---|---|---|
Absolute minimum temperature (ºC) | -3 | |
Mean annual temperature (ºC) | 10 | 35 |
Rainfall
Top of pageParameter | Lower limit | Upper limit | Description |
---|---|---|---|
Mean annual rainfall | 200 | 1060 | mm; lower/upper limits |
Soil Tolerances
Top of pageSoil drainage
- free
Soil reaction
- acid
- neutral
Soil texture
- light
- medium
Special soil tolerances
- shallow
Notes on Natural Enemies
Top of pageIn Venezuela, plants of S. seaforthianum have been found naturally infected with eggplant mosaic virus (EMV). Diseased plants showed mottling, vein-banding, and little or no distortion. According to the authors, this was the first report of EMV naturally infecting an indigenous host in the warm tropics (Debrot et al., 1977).
Means of Movement and Dispersal
Top of pageS. seaforthianum spreads by seeds. Fruits can be dispersed by birds, cattle, and water (Gallagher et al., 2010; Queensland Department of Primary Industries and Fisheries, 2011; BioNET-EAFRINET, 2014).
Pathway Causes
Top of pageCause | Notes | Long Distance | Local | References |
---|---|---|---|---|
Disturbance | Grown as a weed | Yes | Yes | Randall (2012) |
Escape from confinement or garden escape | Planted as ornamental. Seeds dispersed by birds. | Yes | Yes | Gallagher et al. (2010) |
Horticulture | Planted as ornamental. Seeds dispersed by birds. | Yes | Yes | Gallagher et al. (2010) |
Internet sales | Seeds and plants sold online | Yes | Yes | |
Nursery trade | Planted as ornamental | Yes | Yes | Gallagher et al. (2010) |
Ornamental purposes | Planted as ornamental | Yes | Yes | Gallagher et al. (2010) |
Pathway Vectors
Top of pageVector | Notes | Long Distance | Local | References |
---|---|---|---|---|
Machinery and equipment | Weed in pastures | Yes | Yes | Queensland Department of Primary Industries and Fisheries (2011) |
Soil, sand and gravel | Seeds as a soil-contaminant | Yes | Yes | Gallagher et al. (2010) |
Water | Seeds | Yes | Yes | Gallagher et al. (2010) |
Impact Summary
Top of pageCategory | Impact |
---|---|
Economic/livelihood | Positive and negative |
Environment (generally) | Positive and negative |
Human health | Negative |
Environmental Impact
Top of pageS. seaforthianum is considered an invasive and noxious weed with the potential to overtop and smother native plant communities. This species out-competes native plant species by crowding or shading them out (ISSG, 2008; Queensland Department of Primary Industries and Fisheries, 2011; PIER, 2014). S. seaforthianum also reduces biodiversity in natural forests because plants are able to dominate large areas in the understory affecting the germination and establishment of native species. In South Africa for example, it is invading areas with high conservation relevance such as the Kruger National Park (Foxcroft et al., 2003). S. seaforthianum is poisonous and children and poultry have been adversely affected after eating its fruit. Cattle, pigs and sheep have also been affected by this species (Queensland Department of Primary Industries and Fisheries, 2011; USDA-ARS, 2014).
Risk and Impact Factors
Top of page- Proved invasive outside its native range
- Highly adaptable to different environments
- Is a habitat generalist
- Tolerates, or benefits from, cultivation, browsing pressure, mutilation, fire etc
- Pioneering in disturbed areas
- Highly mobile locally
- Benefits from human association (i.e. it is a human commensal)
- Long lived
- Fast growing
- Damaged ecosystem services
- Ecosystem change/ habitat alteration
- Host damage
- Infrastructure damage
- Monoculture formation
- Negatively impacts animal health
- Reduced native biodiversity
- Threat to/ loss of native species
- Damages animal/plant products
- Competition - monopolizing resources
- Competition - shading
- Competition - smothering
- Competition - strangling
- Pest and disease transmission
- Poisoning
- Rapid growth
- Highly likely to be transported internationally deliberately
Uses
Top of pageS. seaforthianum has been widely commercialized as a garden ornamental plant (USDA-ARS, 2014).
Uses List
Top of pageEnvironmental
- Amenity
General
- Ornamental
Materials
- Poisonous to mammals
Ornamental
- Potted plant
- Propagation material
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.
S. seaforthianum is difficult to eradicate and the best management strategy varies according to the infestation size. Individual plants and small infestations should be pulled up and burned completely along with all fruit. Larger infestations require repeated mowing and/or repeated applications of herbicides. It is important that plants are not allowed to fruit in order to prevent seed dispersal. There are no specific herbicides recommended for the treatment of this species, however, triclopyr, aminopyralid, 2,4-D and picloram have been used for the chemical control of the closely related species Solanum viarum (Waggy, 2009.)
References
Top of pageAcevedo-Rodríguez P, Strong MT, 2012. Catalogue of the Seed Plants of the West Indies. Smithsonian Contributions to Botany, 98:1192 pp. Washington DC, USA: Smithsonian Institution. http://botany.si.edu/Antilles/WestIndies/catalog.htm
Bello Espinosa D, 1881. [English title not available]. (Apuntes para la flora de Puerto Rico. Primera parte.) Anal. Soc. Española de Hist. Nat, 10:231-304
BioNET-EAFRINET, 2014. East African Network for Taxonomy. Online Key and Fact Sheets for Invasive plants. http://keys.lucidcentral.org/keys/v3/eafrinet/weeds/key/weeds/Media/Html/index.htm
Broome R, Sabir K, Carrington S, 2007. Plants of the Eastern Caribbean. Online database. Barbados: University of the West Indies. http://ecflora.cavehill.uwi.edu/index.html
Chandra SK, 2012. Invasive Alien Plants of Indian Himalayan Region- Diversity and Implication. American Journal of Plant Sciences, 3:177-184
Crane JH, Balerdi CF, Klassen W, 2008. Section 4: Common weeds found in tropical fruit orchards in South Florida, USA. Major problems affecting agriculture in Miami-Dade agriculture and emerging technological developments. 33-54. http://www.agmarketing.ifas.ufl.edu/dlfiles/DadeAgLandRetentionAppendixVolumeE.pdf
Eggers HFA, 1879. The Flora of St. Croix and the Virgin Islands. Washington, USA: Washington Government Printing Office, 148 pp
Flora of China Editorial Committee, 2014. Flora of China. St. Louis, Missouri and Cambridge, Massachusetts, USA: Missouri Botanical Garden and Harvard University Herbaria. http://www.efloras.org/flora_page.aspx?flora_id=2
Flora of Taiwan Editorial Committee, 2013. Digital flora of Taiwan. http://www.efloras.org/flora_page.aspx?flora_id=100
Florence J, Chevillotte H, Ollier C, Meyer J-Y, 2013. Base de données botaniques Nadeaud de l'Herbier de la Polynésie Française (PAP) (Botanical database of the Nadeaud Herbarium of French Polynesia). http://www.herbier-tahiti.pf
Gentry Jr JL, Standley PC, 1974. Solanaceae. Fieldiana Botany, 24:1-151. [Flora of Guatemala - Part X, Numbers 1 and 2.]
Howard RA, 1979. Early botanical records from the West Indies, particularly Barbados: Ligon (1657) to Lord Seaforth (1806). Botanical Journal of the Linnean Society, 79:65-96
ISSG, 2008. Global Invasive Species Database (GISD). http://www.issg.org/database
Knapp S, 2010. Solanum seaforthianum. PBI Solanum Source: A worldwide treatment. http://www.nhm.ac.uk/research-curation/research/projects/solanaceaesource/
Mbale H, 2010. Checklist of Invasive Plants of the Congo. Discover Life. http://www.discoverlife.org/mp/20q?guide=Invasive_plants_of_Congo
Nee M, 1999. Synopsis of Solanum in the New World. In: Solanaceae IV [ed. by Nee, M. \Lester, R. N. \Jessop, J. P.]. Richmond, Surrey, UK: Kew Royal Botanic Gardens, 285-333
Oviedo Prieto R, Herrera Oliver P, Caluff MG, et al. , 2012. National list of invasive and potentially invasive plants in the Republic of Cuba - 2011. (Lista nacional de especies de plantas invasoras y potencialmente invasoras en la República de Cuba - 2011). Bissea: Boletín sobre Conservación de Plantas del Jardín Botánico Nacional de Cuba, 6(Special Issue 1):22-96
Pauwels L, 2012. Plantes cultivées et/ou exotiques en Afrique Centrale: R.D. Congo-Rwanda-Burindi ([English title not available]). http://users.telenet.be/cr28796/CultAfrC.htm
Peekel PG, 1984. Flora of the Bismarck Archipelago for naturalists. Lae, Papua New Guinea: Office of Forests, Division of Botany, 638 pp
PIER, 2014. Pacific Islands Ecosystems at Risk. Honolulu, USA: HEAR, University of Hawaii. http://www.hear.org/pier/index.html
PROTA, 2014. PROTA4U web database. Grubben GJH, Denton OA, eds. Wageningen, Netherlands: Plant Resources of Tropical Africa. http://www.prota4u.org/search.asp
Queensland Department of Primary Industries and Fisheries, 2011. Special edition of Environmental Weeds of Australia for Biosecurity Queensland., Australia: The University of Queensland and Department of Primary Industries and Fisheries. http://keyserver.lucidcentral.org/weeds/data/03030800-0b07-490a-8d04-0605030c0f01/media/Html/Index.htm
Randall RP, 2012. A Global Compendium of Weeds. Perth, Australia: Department of Agriculture and Food Western Australia, 1124 pp. http://www.cabi.org/isc/FullTextPDF/2013/20133109119.pdf
Sarkar AK, Datta N, Chatterjee U, 1980. Chromosome number reports LXVII. Taxon, 29:360-361
Stehmann JR, Mentz LA, Agra MF, Vignoli-Silva M, Giacomin L, Rodrigues IMC, 2014. Solanaceae in Lista de Espécies da Flora do Brasil (Solanum in list of species of the flora of Brazil). Rio de Janeiro, Brazil: Jardim Botânico do Rio de Janeiro. http://reflora.jbrj.gov.br/jabot/floradobrasil/FB127323
Stevens PF, 2012. Angiosperm Phylogeny Website. http://www.mobot.org/MOBOT/research/APweb/
Urban I, 1905. Symbolae Antillanae. Volumen IV. Berlin, Germany: Fratres Borntraeger, 771 pp
USDA-ARS, 2014. Germplasm Resources Information Network (GRIN). Online Database. Beltsville, Maryland, USA: National Germplasm Resources Laboratory. https://npgsweb.ars-grin.gov/gringlobal/taxon/taxonomysearch.aspx
USDA-NRCS, 2014. The PLANTS Database. Baton Rouge, USA: National Plant Data Center. http://plants.usda.gov/
Waggy MA, 2009. Solanum viarum. Fire Effects Information System, [Online]., USA: U.S. Department of Agriculture, Forest Service, Rocky Mountain Research Station, Fire Sciences Laboratory. http://www.fs.fed.us/database/feis
Wagner WL, Herbst DR, Sohmer SH, 1999. Manual of the flowering plants of Hawaii. Revised edition. Honolulu, Hawai'i, USA: Bishop Museum Press, 1919 pp
Weese TL, Bohs L, 2007. A three-gene phylogeny of the genus Solanum (Solanaceae). Systematic Botany, 32:445-463
Wunderlin RP, Hansen BF, 2008. Atlas of Florida Vascular Plants. Florida, USA: University of South Florida. http://www.plantatlas.usf.edu/
Distribution References
BioNET-EAFRINET, 2014. East African Network for Taxonomy. In: Online Key and Fact Sheets for Invasive plants, http://keys.lucidcentral.org/keys/v3/eafrinet/weeds/key/weeds/Media/Html/index.htm
Broome R, Sabir K, Carrington S, 2007. Plants of the Eastern Caribbean. Online database., Barbados: University of the West Indies. http://ecflora.cavehill.uwi.edu/index.htm
CABI, Undated. CABI Compendium: Status inferred from regional distribution. Wallingford, UK: CABI
CABI, Undated a. CABI Compendium: Status as determined by CABI editor. Wallingford, UK: CABI
Chandra SK, 2012. Invasive Alien Plants of Indian Himalayan Region- Diversity and Implication. In: American Journal of Plant Sciences, 3 177-184.
Flora of Taiwan Editorial Committee, 2013. Digital flora of Taiwan., http://www.efloras.org/flora_page.aspx?flora_id=100
Florence J, Chevillotte H, Ollier C, Meyer J-Y, 2013. Botanical database of the Nadeaud Herbarium of French Polynesia. (Base de données botaniques Nadeaud de l'Herbier de la Polynésie Française (PAP))., http://www.herbier-tahiti.pf
Gentry Jr JL, Standley PC, 1974. Solanaceae. Flora of Guatemala - Part X, Numbers 1 and 2. In: Fieldiana Botany, 24 1-151.
Pauwels L, 2012. [English title not available]. (Plantes cultivées et/ou exotiques en Afrique Centrale: R.D. Congo-Rwanda-Burindi)., http://users.telenet.be/cr28796/CultAfrC.htm
Peekel PG, 1984. Flora of the Bismarck Archipelago for naturalists., Lae, Papua New Guinea: Office of Forests, Division of Botany. 638 pp.
PIER, 2014. Pacific Islands Ecosystems at Risk., Honolulu, USA: HEAR, University of Hawaii. http://www.hear.org/pier/index.html
PROTA, 2014. PROTA4U web database., [ed. by Grubben GJH, Denton OA]. Wageningen, Netherlands: Plant Resources of Tropical Africa. http://www.prota4u.org/search.asp
Queensland Department of Primary Industries and Fisheries, 2011. Special edition of Environmental Weeds of Australia for Biosecurity Queensland., Australia: The University of Queensland and Department of Primary Industries and Fisheries. http://keyserver.lucidcentral.org/weeds/data/03030800-0b07-490a-8d04-0605030c0f01/media/Html/Index.htm
Stehmann JR, Mentz LA, Agra MF, Vignoli-Silva M, Giacomin L, Rodrigues IMC, 2014. Solanum in list of species of the flora of Brazil. (Solanaceae in Lista de Espécies da Flora do Brasil)., Rio de Janeiro, Brazil: Jardim Botânico do Rio de Janeiro. http://reflora.jbrj.gov.br/jabot/floradobrasil/FB127323
USDA-ARS, 2014. Germplasm Resources Information Network (GRIN). Online Database. Beltsville, Maryland, USA: National Germplasm Resources Laboratory. https://npgsweb.ars-grin.gov/gringlobal/taxon/taxonomysimple.aspx
Wagner WL, Herbst DR, Sohmer SH, 1999. Manual of the flowering plants of Hawaii. Revised edition., Honolulu, Hawai'i, USA: Bishop Museum Press. 1919 pp.
Wunderlin RP, Hansen BF, 2008. Atlas of Florida Vascular Plants., Florida, USA: University of South Florida. http://www.plantatlas.usf.edu/
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. |
Contributors
Top of page24/03/14 Original text by:
Julissa Rojas-Sandoval, Department of Botany-Smithsonian NMNH, Washington DC, USA
Pedro Acevedo-Rodríguez, Department of Botany-Smithsonian NMNH, Washington DC, USA
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