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Acanthospermum australe (spiny-bur)
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Pictures
Top of page| Picture | Title | Caption | Copyright |  | Title | Fruits |
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| Caption | Acanthospermum australe (spiny-bur); close view of fruits and a flower. Honeydew, Gauteng, South Africa. February 2016. |
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| Copyright | ©Paul Venter-2016/via wikipedia - CC BY-SA 3.0 |
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| Fruits | Acanthospermum australe (spiny-bur); close view of fruits and a flower. Honeydew, Gauteng, South Africa. February 2016. | ©Paul Venter-2016/via wikipedia - CC BY-SA 3.0 |
 | Title | Habit |
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| Caption | Acanthospermum australe (spiny-bur); habit. Kukumamalu gulch, Molokai, Hawaii, USA. May, 2005. |
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| Copyright | ©Forest & Kim Starr-2005 - CC BY 3.0 |
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| Habit | Acanthospermum australe (spiny-bur); habit. Kukumamalu gulch, Molokai, Hawaii, USA. May, 2005. | ©Forest & Kim Starr-2005 - CC BY 3.0 |
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| Caption | Acanthospermum australe (spiny-bur); habit. Polihua Rd, Lanai, Hawaii, USA. April, 2007. |
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| Copyright | ©Forest & Kim Starr-2007 - CC BY 3.0 |
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| Habit | Acanthospermum australe (spiny-bur); habit. Polihua Rd, Lanai, Hawaii, USA. April, 2007. | ©Forest & Kim Starr-2007 - CC BY 3.0 |
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| Caption | Acanthospermum australe (spiny-bur); habit, with flowers. Hanaula, Maui, Hawaii, USA. September, 2011. |
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| Copyright | ©Forest & Kim Starr-2011 - CC BY 3.0 |
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| Habit | Acanthospermum australe (spiny-bur); habit, with flowers. Hanaula, Maui, Hawaii, USA. September, 2011. | ©Forest & Kim Starr-2011 - CC BY 3.0 |
 | Title | Flowers and leaves |
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| Caption | Acanthospermum australe (spiny-bur); flowers and leaves. Hanaula, Maui, Hawaii, USA. September, 2011. |
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| Copyright | ©Forest & Kim Starr-2011 - CC BY 3.0 |
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| Flowers and leaves | Acanthospermum australe (spiny-bur); flowers and leaves. Hanaula, Maui, Hawaii, USA. September, 2011. | ©Forest & Kim Starr-2011 - CC BY 3.0 |
Identity
Top of pagePreferred Scientific Name
- Acanthospermum australe (Loefl.) Kuntze
Preferred Common Name
Other Scientific Names
- Acanthospermum brasilum Schrank.
- Acanthospermum hirsutum DC.
- Acanthospermum xanthioides (Kunth) DC.
- Echinodium prostratum Poit.
- Melampodium australe Loefl.
- Orcya adhaerens Vell.
- Orcya adhaerescens Vell.
International Common Names
- English: creeping starbur; guay greenstripe; Paraguayan starbur; Paraguay-bur; Paraguay-starbur; sheep-bur; spiny bur; star bur
Local Common Names
- Brazil: amor-de-negro; carrapichinho; carrapicho-rasteiro; cordao de sapochifrinho; maroto; mata-pasto; tapekué
- Hawaii: ‘ihi kukae hipa; kukaehipa; pipili
- Paraguay: tapeku
- South Africa: donkieklits; eight-seeded starbur; jodeluis; kruipsterklits; setla-bocha
Summary of Invasiveness
Top of page
Acanthospermum australe is a creeping annual or short-lived perennial plant, which originates from the tropics and sub-tropics of Central and South America. A. australe has been introduced to China, Australia, Africa, and the USA, where it is classed as invasive in the states of Hawaii and Oregon. It spreads to form dense mats that can smother other low-growing vegetation. In Australia, A. australe is seen as a threat to native mat-forming species in coastal sand dunes and in hind-dune vegetation. It is also regarded as an invasive species within its native range in Brazil, where it occurs in conservation areas.
Taxonomic Tree
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- Domain: Eukaryota
- Kingdom: Plantae
- Phylum: Spermatophyta
- Subphylum: Angiospermae
- Class: Dicotyledonae
- Order: Asterales
- Family: Asteraceae
- Genus: Acanthospermum
- Species: Acanthospermum australe
Description
Top of page
Annual or short-term perennial, stems 10-60(-120) cm, mostly procumbent. Leaves cauline. Leaves rhombic-ovate to triangular, 1.5-3.5 cm long, 1-3 cm wide, with conspicuous glands on both surfaces, margins irregularly serrate above the middle, base cuneate, petioles 0.3-1.5 cm long. Heads 4-6 mm in diameter, generally solitary, with 3-8 white-cream-yellow ray florets and 3-8 yellowish disc florets functionally staminate. The single-seeded fruits (cypselae) are each enclosed within and shed with an often hardened, ± prickly perigynium, ultimately plumply ellipsoid to fusiform, or ± compressed (PIER, 2015; PROTA, 2015; ZipcodeZoo, 2015).
A. australe has small stomata and 4-5-cellular non-glandular hairs (Martins et al., 2006).
Plant Type
Top of pageAnnual
Broadleaved
Herbaceous
Seed propagated
Vegetatively propagated
Distribution
Top of page
A. australe is native to South and Central America, but has been introduced widely to Mexico and USA, including Hawaii. Distribution is generally localized in China and Australia, and mostly sporadic in a number of countries in Africa. GBIF (2015) has single records from many African countries, perhaps suggesting some mis-identification. GBIF (2015) records for A. australe in South Africa and Swaziland include multiple specimens. Contrastingly, there are no occurrences of A. australe listed in these countries in Flora Zambesiaca (2015).
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.
| Country | Distribution | Last Reported | Origin | First Reported | Invasive | References | Notes | ASIA |
| China | Localised | | Introduced | | Invasive | Liu et al., 2006; GBIF, 2015 | |
| -Yunnan | Present | | Introduced | | | Missouri Botanical Garden, 2015 | |
AFRICA |
| Cameroon | Localised | | Introduced | | | GBIF, 2015 | |
| Congo | Localised | | Introduced | | | GBIF, 2015 | |
| Ghana | Localised | | Introduced | | | GBIF, 2015 | |
| Kenya | Localised | | Introduced | | | GBIF, 2015 | One collection only |
| Madagascar | Present | | Introduced | | | GBIF, 2015 | One collection only |
| Malawi | Present | | Introduced | | | GBIF, 2015 | One collection only |
| Mozambique | Present | | Introduced | | | GBIF, 2015 | One collection only |
| Nigeria | Localised | | Introduced | | | GBIF, 2015 | |
| South Africa | Present | | Introduced | | | USDA-ARS, 2015 | |
| Swaziland | Present | | Introduced | | | USDA-ARS, 2015 | |
| Tanzania | Localised | | Introduced | | | GBIF, 2015 | |
| Zimbabwe | Localised | | Introduced | | | GBIF, 2015 | One collection only |
NORTH AMERICA |
| Mexico | Present | | Introduced | | Invasive | PIER, 2015 | |
| USA | Present | | Introduced | | Invasive | PIER, 2015 | |
| -Alabama | Present | | Introduced | | | USDA-ARS, 2015 | |
| -Arkansas | Present | | Introduced | | | USDA-ARS, 2015 | |
| -District of Columbia | Present | | Introduced | | | USDA-ARS, 2015 | |
| -Florida | Present | | Introduced | | | USDA-ARS, 2015 | |
| -Georgia | Present | | Introduced | | | USDA-ARS, 2015 | |
| -Hawaii | Widespread | | Introduced | | Invasive | PIER, 2015 | Big, Kaho‘olawe, Kaua‘I, Lana‘I, Maui, Moloka’I, Ni‘ihau, O’ahi islands |
| -Louisiana | Present | | Introduced | | | USDA-ARS, 2015 | |
| -Massachusetts | Present | | Introduced | | | USDA-ARS, 2015 | |
| -Mississippi | Present | | Introduced | | | BONAP, 2015 | |
| -New Jersey | Present | | Introduced | | | BONAP, 2015 | |
| -North Carolina | Present | | Introduced | | | BONAP, 2015 | |
| -Oregon | Present | | Introduced | | Invasive | PIER, 2015 | |
| -Pennsylvania | Present | | Introduced | | | USDA-ARS, 2015 | |
| -South Carolina | Present | | Introduced | | | USDA-ARS, 2015 | |
| -Tennessee | Present | | Introduced | | | BONAP, 2015 | |
| -Texas | Present | | Introduced | | | USDA-ARS, 2015 | |
| -Virginia | Present | | Introduced | | | USDA-ARS, 2015 | |
CENTRAL AMERICA AND CARIBBEAN |
| Grenada | Present | | Native | | | USDA-ARS, 2015 | |
| Martinique | Present | | Native | | | USDA-ARS, 2015 | |
| Saint Vincent and the Grenadines | Present | | Native | | | USDA-ARS, 2015 | |
SOUTH AMERICA |
| Argentina | Present | | Native | | | USDA-ARS, 2015 | |
| Bolivia | Present | | Native | | | USDA-ARS, 2015 | |
| Brazil | Widespread | | Native | | | USDA-ARS, 2015 | |
| -Acre | Present | | Native | | | Lorenzi, 1982 | |
| -Alagoas | Present | | Native | | | Lorenzi, 1982 | |
| -Amapa | Present | | Native | | | Lorenzi, 1982 | |
| -Amazonas | Present | | Native | | | Lorenzi, 1982 | |
| -Bahia | Present | | Native | | | Lorenzi, 1982 | |
| -Ceara | Present | | Native | | | Lorenzi, 1982 | |
| -Espirito Santo | Present | | Native | | | Lorenzi, 1982 | |
| -Fernando de Noronha | Present | | Native | | | Lorenzi, 1982 | |
| -Goias | Present | | Native | | | Lorenzi, 1982 | |
| -Maranhao | Present | | Native | | | Lorenzi, 1982 | |
| -Mato Grosso | Present | | Native | | | Lorenzi, 1982 | |
| -Mato Grosso do Sul | Present | | Native | | | Lorenzi, 1982 | |
| -Minas Gerais | Present | | Native | | | Lorenzi, 1982 | |
| -Para | Present | | Native | | | Lorenzi, 1982 | |
| -Paraiba | Present | | Native | | | Lorenzi, 1982 | |
| -Parana | Present | | Native | | | Lorenzi, 1982 | |
| -Pernambuco | Present | | Native | | | Lorenzi, 1982 | |
| -Piaui | Present | | Native | | | Lorenzi, 1982 | |
| -Rio de Janeiro | Present | | Native | | | Lorenzi, 1982 | |
| -Rio Grande do Norte | Present | | Native | | | Lorenzi, 1982 | |
| -Rio Grande do Sul | Present | | Native | | | Lorenzi, 1982 | |
| -Rondonia | Present | | Native | | | Lorenzi, 1982 | |
| -Roraima | Present | | Native | | | Lorenzi, 1982 | |
| -Santa Catarina | Present | | Native | | | Lorenzi, 1982 | |
| -Sao Paulo | Present | | Native | | | Lorenzi, 1982 | |
| -Sergipe | Present | | Native | | | Lorenzi, 1982 | |
| -Tocantins | Present | | Native | | | Lorenzi, 1982 | |
| Colombia | Present | | Native | | | USDA-ARS, 2015 | |
| Ecuador | Present | | Native | | | GBIF, 2015 | |
| French Guiana | Present | | Native | | | USDA-ARS, 2015 | |
| Guyana | Present | | Native | | | USDA-ARS, 2015 | |
| Paraguay | Present | | Native | | | USDA-ARS, 2015 | |
| Peru | Present | | Native | | | GBIF, 2015 | |
| Suriname | Present | | Native | | | USDA-ARS, 2015 | |
| Uruguay | Present | | Native | | | USDA-ARS, 2015 | |
| Venezuela | Present | | Native | | | USDA-ARS, 2015 | |
OCEANIA |
| Australia | Present | | Introduced | | Invasive | PIER, 2015 | |
| -New South Wales | Present | | Introduced | | Invasive | PIER, 2015 | |
| -Queensland | Present | | Introduced | | | Technigro, 2010 | |
History of Introduction and Spread
Top of page
In the USA, early introductions of A. australe occurred in Alabama and Hawaii in 1877 and 1895, respectively. In Australia, it was first recorded in New South Wales in 1967 (Benson and McDougall, 1994), and in Queensland in 1994 (Technigro, 2010). However, the origins of these introductions are not detailed.
Habitat
Top of page
A. australe, a plant of disturbed ground, commonly occurs on roadsides and in crops in its native South America. In Hawai’i it is naturalized along roadsides and other relatively dry, open, disturbed areas (PIER, 2015). In Australia it occurs on sand dunes and sandy soils along footpaths and roadsides in the near-coastal areas (Technigro, 2010).
Habitat List
Top of page| Category | Habitat | Presence | Status | | Littoral |
| Coastal areas | Secondary/tolerated habitat | |
| Coastal dunes | Principal habitat | |
| Terrestrial-managed |
| Cultivated / agricultural land | Principal habitat | |
| Disturbed areas | Principal habitat | |
| Managed grasslands (grazing systems) | Secondary/tolerated habitat | |
| Rail / roadsides | Principal habitat | |
| Urban / peri-urban areas | Secondary/tolerated habitat | |
| Terrestrial-natural/semi-natural |
| Natural grasslands | Secondary/tolerated habitat | |
| Rocky areas / lava flows | Secondary/tolerated habitat | |
| Scrub / shrublands | Secondary/tolerated habitat | |
Hosts/Species Affected
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A. australe is a frequent and sometimes dominant weed of crops in its native area in South America, particularly in Brazil where it is recorded in Phaseolus beans, rice, cotton, groundnut, maize, cassava, okra and tomatoes.
In Hawaii, the endangered Poa mannii on the island of Kauai is threatened by a number of invasive plants, including A. australe (USFWS, 2008).
Growth Stages
Top of pageSeedling stage, Vegetative growing stage
Biology and Ecology
Top of page
Genetics
The chromosome number of A. australe has been found as 2n = 20 and 22 (Missouri Botanical Garden, 2015). Other sources usually indicate 2n = 22.
Reproductive Biology
In the cogeneric A. hispidum, self-pollination and cross-pollination occur by wind. A. australe is assumed to have similar pollination behaviour, since it is also monoecious, having male flowers in the centre and female flowers on the outside of the inflorescence. However, it is also known to be pollinated by bees (Isahara and Miamoni-Rodell, 2011).
Very little information is available on the germination of A. australe seeds, but B & T World Seeds (2015) suggest that it may be stimulated by smoke.
Vegetative propagation can occur from the prostrate stems (Technigro, 2010).
Physiology and Phenology
As a member of the Heliantheae (tribe Asteraceae), A. australe is known to have C4 physiology.
Longevity
Longevity of the plant is not normally more than one year. However, although A. australe is generally referred to as an annual, Technigro (2010) describes it as ‘long-lived’ and refers to the dangers of vegetative propagation, presumably from the prostrate stems.
Associations
The following endophytic fungi have been found to have associations with A. australe in Argentina: Alternaria alternata, Aureobasidium pullulans, Fusarium oxysporum, F. solani, Myrothecium roridum, Phoma sp. and Sordaria fimicola. It is suggested that some of these may have significance in medicinal terms (Giusiano et al., 2010).
Environmental Requirements
A. australe thrives in warm, relatively dry conditions.
Climate
Top of page| Climate | Status | Description | Remark | | Am - Tropical monsoon climate | Tolerated | 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 | |
| Cf - Warm temperate climate, wet all year | Preferred | Warm average temp. > 10°C, Cold average temp. > 0°C, wet all year | |
| Cw - Warm temperate climate with dry winter | Preferred | Warm temperate climate with dry winter (Warm average temp. > 10°C, Cold average temp. > 0°C, dry winters) | |
Latitude/Altitude
Top of page| Latitude North (°N) | Latitude South (°S) | Altitude Lower (m) | Altitude Upper (m) | | 35 | 35 | | |
Soil Tolerances
Top of pageSoil drainage
Soil reaction
Soil texture
Special soil tolerances
Notes on Natural Enemies
Top of page
A. australe is an alternate host of Thanatephorus cucumeris, the causal agent of web blight on dry beans, and the plants are quite severely affected (Costa et al., 2007). No other natural enemies are commonly reported.
Means of Movement and Dispersal
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Vector Transmission
A. australe is readily transported by livestock due to the spiky burs, which attach themselves to the coats/tails.
Accidental Introduction
Accidental introduction can occur via the import of pelts or wool of livestock.
Intentional Introduction
Intentional introduction is unlikely. The plant’s applications in medicine are generally known only locally, where the weed already occurs, so the risk of introduction outside of these areas is minimal.
Pathway Causes
Top of page| Cause | Notes | Long Distance | Local | References | | Agriculture | | Yes | Yes | |
| Animal production | | | Yes | |
| Harvesting fur/wool/hair | | | Yes | |
| Hitchhiker | | Yes | Yes | |
Pathway Vectors
Top of page| Vector | Notes | Long Distance | Local | References | | Clothing/footwear and possessions | | Yes | Yes | |
| Hides/trophies/ feathers | | Yes | Yes | |
| Land vehicles | | | Yes | |
| Livestock | | | Yes | |
| Machinery/equipment | | | Yes | |
Impact Summary
Top of page| Category | Impact | | Economic/livelihood | Negative |
| Environment (generally) | Negative |
| Human health | Positive |
Economic Impact
Top of page
A. australe is a major weed of crops, especially in Brazil. These include soybean, Phaseolus beans, rice, cotton, groundnut, maize, cassava, okra and tomatoes, but there are no exact estimates of the losses caused.
It is also an alternate host of Thanatephorus cucumeris, the causal agent of web blight on dry beans (Costa et al., 2007).
Environmental Impact
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A. australe is regarded as an environmental weed in Australia, where it can threaten the native vegetation of sand dunes (Technigro, 2010). In Hawaii it is among the group of invasive species threatening the endangered grass Poa mannii on the island of Kauai (USFWS, 2008).
Risk and Impact Factors
Top of pageImpact mechanisms
- Competition
- Competition - smothering
- Produces spines, thorns or burrs
Impact outcomes
- Negatively impacts agriculture
- Reduced native biodiversity
- Threat to/ loss of native species
Invasiveness
- Abundant in its native range
- Has a broad native range
- Highly adaptable to different environments
- Invasive in its native range
- Pioneering in disturbed areas
- Proved invasive outside its native range
- Reproduces asexually
Likelihood of entry/control
- Highly likely to be transported internationally accidentally
Uses
Top of page
Social Benefit
A. australe has a wide range of traditional medicinal uses, with supposed activity against: the protozoan Acanthamoeba polyphaga trophozoites (Castro et al., 2013); a range of fungi causing skin diseases in Paraguay (Portillo et al., 2001) and specifically Candida albicans in Brazil (Fabri et al., 2011); rheumatism and arthritis (by internal administration); and swelling and bleeding (by external application) (Shimizu et al., 1987); malaria in South Africa (Nethengwe et al., 2012); herpes and polio viruses (Martins et al., 2011); and for anti-fertility, foot problems and sores (Duke, 2015). Hepatoprotective properties have also been reported.
The basis for these uses has not been explained, but Carvalho et al. (2014) have confirmed antimicrobial activity of oil from A. australe, and high antioxidant activity was confirmed in Argentina (Desmarchelier et al., 1997). The detection of high concentrations of caffeoylquinic acids in the plants indicated that their use in traditional medicine is justified (Debenedetti et al., 1993). Acanthostral, a novel germacranolide, was isolated as an antineoplastic constituent from the above-ground parts of A. australe, showing significant activity against L1210 (murine leukaemia) cell cultures (Matsunaga et al., 1996).
Similarities to Other Species/Conditions
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A. australe is similar to A. hispidum, but the latter can be distinguished by its upright habit and the fact that its fruits have two larger spines at their tips. A short petiole in A. hispidum is another diagnostic trait that distinguishes it from A. australe. Types of glandular trichomes can also be used to distinguish these two species (Araújo et al., 2013).
Prevention and Control
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Cultural Control and Sanitary Measures
It is especially important to avoid the spread of A. australe by the sticky burs on animal coats or human clothing.
Physical/Mechanical Control
A. australe can be controlled mechanically in the early stages of growth, but this becomes more difficult as the plant matures and becomes woody at the base.
Movement Control
Avoid transfer by grazing animals and in human clothing.
Chemical Control
A. australe is controlled by glyphosate in non-crop situations and in glyphosate-tolerant soybeans. Other herbicides of use in soybean include: a mixture of diclosulam and flumetsulam (Fortuna and Dutra,1999); chlorimuron-ethyl plus metribuzin (with or without cyanazine) (Guimarães, 1988); and sethoxydim plus bentazone (sethoxydim is not effective on its own).
Herbicides for other crops include: benthiocarb (thiobencarb) + propanil, propanil + 2,4-D, propanil + oxadiazon (for rice); diuron +/- sethoxydim, paraquat (for cotton); trifluralin (for okra).
A. australe apparently has an unusual susceptibility to fluazifop-butyl (Zhang and Luo, 2010), a characteristic which could be of value in a range of broad-leaved crops.
Gaps in Knowledge/Research Needs
Top of page
There is a scarcity of information on many aspects of this weed, particularly its environmental requirements, germination requirements, and seed longevity.
References
Top of pageAraújo Ede L, Xavier HS, Ferreira CP, Randau KP, Pimentel RMde M, 2013. Macro and microscopical identification of two Acanthospermum medicinal plants. Journal of Medicinal Plants Research, 7(35):2606-2615. http://www.academicjournals.org/JMPR/PDF/pdf2013/17Sept/Araujo%20et%20al.pdf
B & T World Seeds, 2015. Graines de germination induites par fumee. Aigues-Vives, France: B & T World Seeds. http://b-and-t-world-seeds.com/aleCat.asp?title=Graines%20de%20Germination%20Induites%20par%20Fumee&list=185
Benson D, McDougall L, 1994. Ecology of Sydney plant species: Part 2 - Dicotyledon families Asteraceae to Buddlejaceae. Cunninghamia 3:789-1004.
BONAP, 2015. Taxonomic Data Center. North American vascular flora. North Carolina, USA: The Biota of North America Program. http://bonap.net/tdc
Carvalho CCde, Turatti ICC, Lopes NP, Salvador MJ, Nascimento AMdo, 2014. Chemical composition and antimicrobial activity of essential oil from Brazilian plants Acanthospermum australe, Calea fruticosa and Mikania glauca. African Journal of Pharmacy and Pharmacology, 8(14):392-398. http://www.academicjournals.org/article/article1398180439_de%20Carvalho%20et%20al.pdf
Castro LC, Sauter IP, Ethur EM, Kauffmann C, Dall'agnol R, Souza J, Cibulski SP, Muniz AW, Weidlich L, Lohmann PM, Roehe PM, Germani JC, Rott MB, Sand STvand der, 2013. In vitro effect of Acanthospermum australe (Asteraceae) extracts on Acanthamoeba polyphaga trophozoites. Revista Brasileira de Plantas Medicinais, 15(4):589-594. http://www.scielo.br/scielo.php?script=sci_arttext&pid=S1516-05722013000400016&lng=en&nrm=iso&tlng=en
Costa GR, Lobo Júnior M, CaféFilho AC, 2007. Acanthospermum australe is an alternate host of Thanatephorus cucumeris, the causal agent of web blight on dry beans. (Acanthospermum australe é hospedeiro alternativo de Thanatephorus cucumeris, agente causal da mela do feijoeiro.) Fitopatologia Brasileira, 32(1):83. http://www.scielo.br/pdf/fb/v32n1/14.pdf
Debenedetti SL, Palacios PS, Wilson EG, Coussio JD, 1993. HPLC analysis of caffeoylquinic acids content in Argentine medicinal plants. In: Acta Horticulturae, No. 333 [ed. by Franz Ch, Seitz R, Verlet N], 191-199.
Desmarchelier C, Novoa Bermudez MJ, Coussio J, Ciccia G, Boveris A, 1997. Antioxidant and prooxidant activities in aqueous extracts of Argentine plants. International Journal of Pharmacognosy, 35(2):116-120.
Duke J, 2015. Dr. Duke's Phytochemical and Ethnobotanical Databases online resource. Beltsville, USA: Germplasm Resources Information Network (GRIN), National Germplasm Resources Laboratory. http://www.ars-grin.gov/duke/
Fabri RL, Nogueira MS, Dutra LB, Bouzada MLM, Scio E, 2011. Antioxidant and antimicrobial potential of Asteraceae species. (Potencial antioxidante e antimicrobiano de espécies da família Asteraceae.) Revista Brasileira de Plantas Medicinais, 13(2):183-189.
Flora Zambesiaca, 2015. Flora Zambesiaca online (eFloras). Richmond, Surrey, UK: Kew Databases. http://apps.kew.org/efloras/search.do
Fortuna Pde A, Dutra IS, 1999. Effects of a mixture of diclosulam + flumetsulam on Acanthospermum australe (Loef.) Kuntze in Ponta Porã. (Efeitos da mistura diclosulam + flumetsulam sobre Acanthospermum australe (Loef.) Kuntze em Ponta Porã.) In: Documentos - EMBRAPA Agropecuaria Oeste, No. 3 [ed. by Melhorança, A. L.]. 63-66.
Gastauer M, Messias MCTB, Meira Neto JAA, 2012. Floristic composition, species richness and diversity of campo rupestre vegetation from the Itacolomi State Park, Minas Gerais, Brazil. Environment and Natural Resources Research, 2(3):115-130. http://www.ccsenet.org/journal/index.php/enrr/article/view/20125
GBIF, 2015. Global Biodiversity Information Facility. http://www.gbif.org/species
Giusiano G, Rodolfi M, Mangiaterra M, Piontelli E, Picco AM, 2010. Endophytic fungi in medicinal plants of northeast of Argentina. I: Morphotaxonomic approach of their foliar community. (Hongos endófitos en 2 plantas medicinales del nordeste Argentino. I: Análisis morfotaxonómico de sus comunidades foliares.) Boletín Micológico, 25:15-27.
Guimarães SC, 1988. Acanthospermum australe control using a formulation of chlorimuron ethyl and metribuzin, with or without alachlor in soyabeans. (Controle co carrapicho rasteiro (Acanthospermum australe) utilizando formulação de chlorimuron ethyl e metribuzin, com e sem alachlor, na cultura da soja.) Pesquisa em Andamento - Empresa de Pesquisa Agropecuária de Estado de Mato Grosso, No. 15. 3 pp.
Isahara KL, Miamoni-Rodella RCS, 2011. Pollination and dispersal systems in a cerrado remnant (Brazilian Savanna) in southeastern Brazil. Brazilian Archives of Biology and Technology, 54(3):629-642.
Liu Jian, Dong Ming, Miao SL, Li ZhenYu, Song MingHua, Wang RenQing, 2006. Invasive alien plants in China: role of clonality and geographical origin. Biological Invasions, 8(7):1461-1470.
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Contributors
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17/04/15 Original text by:
Chris Parker, Consultant, Bristol, UK
Distribution Maps
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- = Present, no further details
- = Evidence of pathogen
- = Widespread
- = Last reported
- = Localised
- = Presence unconfirmed
- = Confined and subject to quarantine
- = See regional map for distribution within the country
- = Occasional or few reports