Mikania scandens

Pictures

Top of page

Picture

Title

Caption

Copyright

Flowers

Mikania scandens (climbing hempvine); flowers. Loxahatchee National Wildlife Refuge, Florida, USA. September, 2009.

©Forest & Kim Starr-2009 - CC BY 3.0

Habit

Mikania scandens (climbing hempvine); habit, showing flowers and foliage. Loxahatchee National Wildlife Refuge, Florida, USA. September, 2009.

©Forest & Kim Starr-2009 - CC BY 3.0

Leaf

Mikania scandens (climbing hempvine); leaf. John Prince Park, Lake Worth, Florida, USA. September, 2009.

©Forest & Kim Starr-2009 - CC BY 3.0

Flowers and seeds

Mikania scandens (climbing hempvine); flowers and seeds. John Prince Park, Lake Worth, Florida, USA. September, 2009.

©Forest & Kim Starr-2009 - CC BY 3.0

Seeds

Mikania scandens (climbing hempvine); seeds. John Prince Park, Lake Worth, Florida, USA. September, 2009.

©Forest & Kim Starr-2009 - CC BY 3.0

Sprawling habit

Mikania scandens (climbing hempvine); sprawling habit. Alligator Alley, Florida, USA. November, 2003.

©Forest & Kim Starr-2003 - CC BY 3.0

Identity

Top of page

Preferred Scientific Name

Mikania scandens (L.) Willd.

International Common Names

English: climbing hemp weed (USA); louse-plaster
French: liane margoze
Portuguese: guaco-do-jardim; guaco-do-quintal

EPPO code

MIKSC (Mikania scandens)

Summary of Invasiveness

Top of page

M. scandens is a herbaceous climbing vine with the potential to grow over and outcompete native plant species. M. scandens has been purported to be invasive in a number of countries in Southeast Asia and the Pacific Islands (Parker, 1972; Barreto and Evans, 1995), and has been listed as a noxious weed in Hawaii. However, the taxonomic authority of the genus states that the distribution of M. scandens is restricted to North America. It is therefore likely that records outside of this range are a result of misidentifications with the congeneric species M. micrantha; a species known to be invasive and have serious economic and environmental impacts. Unless the identity of M. scandens can be verified in these locations it will remain very difficult to determine this species invasiveness.

In its native range however, M. scandens has been reported to act as a weed on a local scale (e.g., Moon et al., 1993; Anderson et al., 2012) but it is also listed as endangered or extirpated in other parts of its native range (Flora of North America Editorial Committee, 2013; USDA-NRCS, 2013).

Taxonomic Tree

Top of page

Domain: Eukaryota
Kingdom: Plantae
Phylum: Spermatophyta
Subphylum: Angiospermae
Class: Dicotyledonae
Order: Asterales
Family: Asteraceae
Genus: Mikania
Species: Mikania scandens

Notes on Taxonomy and Nomenclature

Top of page

The genus Mikania comprises some 425 species (King and Robinson, 1987), with most of these native to tropical America. With the introduction of Mikania to parts of Asia, there has been some confusion over the identity of the introduced forms as well as over the old world native species, M. cordata (Parker, 1972; Cock, 1982; Barreto and Evans, 1995; Weaver, 2009; Anderson et al., 2012). Although many introduced plants were initially identified as M. scandens (Parker, 1972), the taxonomic authority on the genus, made it clear that M. scandens was restricted to North America, with the introduced plants likely to be M. micrantha (Robinson, 1934). The name M. scandens should be used principally for plants found in eastern USA (Flora of North America Editorial Committee, 2013). Thus many records of the apparent occurrence of M. scandens in Old World locations need to be re-examined, and for the purposes of this review these occurrences will be considered un-verified, despite the fact that many published reports do list M. scandens as occurring in Asia and on Pacific Islands. Several experts working with Mikania agree that this is an ongoing issue and that it is unlikely that M. scandens occurs outside of its native range in North America (W. Holmes, Baylor University, USA, personal communication, 2013; M. Day, Department of Agriculture and Fisheries, Australia, personal communication, 2013; P. Anderson, US Forest Service, USA, personal communication, 2013; C. Parker, Weed Research Organization, UK, personal communication, 2013).

At one time, M. batataefolia was also applied to some Mikania populations in Florida (Holmes, 1975). Given similarities in ecological tolerances, pollen characters, and chromosome counts, M. batataefolia was re-evaluated as synonymous with M. scandens in Florida but not necessarily in the Bahamas (Nauman, 1981).

Description

Top of page

Herbaceous, perennial vine; branching stem obscurely 6-angled to terate, ranging from glabrous to densely pilose; 8-15 cm internodes. Petioles glabrous or puberulent, 20-50 mm. Triangular to triangular-ovate leaf blades, 3-15 x 2-11 cm with cordate to hastate bases; margins subentire to undulate, crenate, or dentate, apices acuminate (tips often caudate), faces puberulent. Produces dense corymbiform flowers, with small heads 5-7 mm long. Corollas generally pinkish to purplish, occasionally white, 3-5.4 mm, dotted sparsely with glands, lobes triangular to deltate. Cypselae dark brown to blackish, 1.8-2.2 mm, also dotted with glands; pappi of 30-37 white or pinkish to purplish bristles 4-4.5 mm. Fruits are oblong 1-.5-2.5 mm long, brownish black, five angled resinous achenes; Chromosome number 2n=38 (Holm et al., 1991; Flora of North America Editorial Committee, 2013).

Plant Type

Top of page

Broadleaved
Herbaceous
Perennial
Seed propagated
Vegetatively propagated
Vine / climber

Distribution

Top of page

M. micrantha is known to occur in all the areas of Asia and the Pacific Islands where M. scandens reportedly occurs (Tripathi et al., 2012). Thus if these Old World records for M. scandens are false, they likely represent occurrences of M. micrantha. The one geographic area where the ranges of M. scandens and M. micrantha are clearly documented to overlap is in Florida, USA (Weaver, 2009; Anderson et al., 2012).

Although there is a record of M. scandens occurring in Ontario, Canada, it has been deleted from the flora of Canada (Scoggan, 1979). The Canadian reports were seemingly based upon misdeterminations and/or "too loose an application of that name with respect to present political boundaries" (Scoggan, 1979).

M. scandens is listed as endangered in Indiana (Bacone and Hedge, 1979), possibly extirpated in Maine, probably extirpated in Michigan and threatened in New Hampshire (USDA-NRCS, 2013). It seems to be extirpated from part of its range in Ohio as well (Holmes, 2006).

Distribution Table

Top 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: 17 Feb 2021

Continent/Country/Region	Distribution	Origin	Reference	Notes
Africa
Madagascar	Absent, Unconfirmed presence record(s)		Novy (1997)
Malawi	Absent, Unconfirmed presence record(s)		Whittle (1996)
Mauritius	Absent, Invalid presence record(s)		CABI (Undated b)
Asia
Bangladesh	Absent, Unconfirmed presence record(s)		Ghani (2003) Uddin et al. (2013)
British Indian Ocean Territory
-Chagos Archipelago	Absent, Unconfirmed presence record(s)		Whistler (1996)
India	Absent, Unconfirmed presence record(s)		Singh et al. (1990)
Indonesia	Absent, Unconfirmed presence record(s)		CABI (Undated b)
-Sumatra	Absent, Unconfirmed presence record(s)		Pratiwi and Nazif (1989)
Malaysia	Absent, Unconfirmed presence record(s)		Matsubayashi et al. (2007) CABI (Undated)
Philippines	Absent, Unconfirmed presence record(s)		CABI (Undated)
Sri Lanka	Absent, Unconfirmed presence record(s)		Piyasena and Dharmaratne (2013)
North America
Bahamas	Present	Native	USDA-ARS (2013)
Canada
-Ontario	Absent, Unconfirmed presence record(s)		Brouillet et al. (2006)	Original record was retracted from the Flora of Canada (Scoggan, 1979 and no subsequent records are available)
Mexico	Present	Native	USDA-ARS (2013)
United States	Present		CABI (Undated a) Diaz et al. (2015)	Present based on regional distribution.
-Alabama	Present	Native	USDA-NRCS (2013)
-Arkansas	Present	Native	USDA-NRCS (2013)
-Connecticut	Present	Native	USDA-NRCS (2013)
-Delaware	Present	Native	USDA-NRCS (2013)
-District of Columbia	Present	Native	USDA-NRCS (2013)
-Florida	Present	Native	USDA-NRCS (2013) Diaz et al. (2015)
-Georgia	Present	Native	USDA-NRCS (2013)
-Illinois	Present	Native	USDA-NRCS (2013)
-Indiana	Present, Localized	Native	USDA-NRCS (2013)	Extirpated (Flora of North America Editorial Committee, 2013)
-Kentucky	Present	Native	USDA-NRCS (2013)
-Louisiana	Present	Native	USDA-NRCS (2013)
-Maine	Present, Localized	Native	USDA-NRCS (2013)	Extirpated (Flora of North America Editorial Committee, 2013)
-Maryland	Present	Native	USDA-NRCS (2013)
-Massachusetts	Present	Native	USDA-NRCS (2013)
-Michigan	Present, Localized	Native	USDA-NRCS (2013)	Extirpated (Flora of North America Editorial Committee, 2013)
-Mississippi	Present	Native	USDA-NRCS (2013)
-Missouri	Present	Native	USDA-NRCS (2013)
-Montana	Present	Native	USDA-NRCS (2013)
-Nevada	Present	Native	USDA-NRCS (2013)
-New Hampshire	Present, Localized	Native	USDA-NRCS (2013)
-New Jersey	Present	Native	USDA-NRCS (2013)
-New York	Present	Native	USDA-NRCS (2013)
-North Carolina	Present	Native	USDA-NRCS (2013)
-Ohio	Present	Native	USDA-NRCS (2013)
-Oklahoma	Present	Native	USDA-NRCS (2013)
-Pennsylvania	Present	Native	USDA-NRCS (2013)
-Rhode Island	Present	Native	USDA-NRCS (2013)
-South Carolina	Present	Native	USDA-NRCS (2013)
-Tennessee	Present	Native	USDA-NRCS (2013)
-Texas	Present	Native	USDA-NRCS (2013)
-Virginia	Present	Native	USDA-NRCS (2013)
Oceania
Federated States of Micronesia	Absent, Unconfirmed presence record(s)		CABI (Undated b)
Guam	Absent, Unconfirmed presence record(s)		Stone (1970) Fosberg et al. (1979)
New Caledonia	Absent, Unconfirmed presence record(s)		MacKee (1994)
Northern Mariana Islands	Absent, Unconfirmed presence record(s)		Fosberg et al. (1979) Raulerson (2006)
Papua New Guinea	Absent, Unconfirmed presence record(s)		Peekel (1984)

History of Introduction and Spread

Top of page

M. scandens is native to temperate to subtropical eastern North America (Flora of North America Editorial Committee, 2013; PIER, 2013). Within Florida, M. scandens may spread locally along ditches and water courses (Moon et al., 1993; Anderson et al., 2012).

There are no confirmed reports of the spread of M. scandens beyond North America however there are numerous records of it being present in Asia and the Pacific. These records are false, due to misidentification of this species.

Risk of Introduction

Top of page

If the records attributed to M. scandens are actually M. micrantha and/or other Mikania species (see Identity section), the risk of introduction of M. scandens is low in the near future since it has no horticultural use at present and does not appear to exhibit extensive long-distance dispersal. M. scandens does thrive in wetlands and can be weedy in areas subject to flooding (Moon et al., 1993), and thus transport of seeds or vegetative plant sections between wetland environments should be avoided.

Habitat

Top of page

Habitats preferred by M. scandens include stream banks and swamps to 500 m in elevation (Anderson et al., 2012) but it also occurs in cloud forests in Mexico at elevations between 1000 and 1500 m (Alvarez-Aquino et al., 2005). In the northern parts of its range, it is present in wetlands but often in low densities (Anderson et al., 1968). M. scandens flourishes in coastal wetland areas in southeastern USA (Herz et al., 1970; Holm et al. 1977), such as coastal marshes in Louisiana (Gough et al., 1994), or bogs in South Carolina (Hunt, 1943). M. scandens is restricted to fresh or oligohaline sites where salt concentrations do not exceed 5 ppt (Gough and Grace, 1997). M. scandens is also found in forests and thickets (Holm et al., 1977), especially wet forested areas such as Louisiana cypress-gum swamp land in Louisiana (Mathies et al., 1983).

Under shady conditions, M. scandens climbs over other vegetation but does not form dense mats (Anderson et al., 2012). It was described as climbing the trees in a Pinus-Juniperus community in Virginia (Harvill, 1965). In White’s (1983) assessment of wetland communities in the Lower Pearl River basin of Louisiana, vines such as M. scandens were associated with scrublands containing woody plants. Tussocks formed by Juncus effusus in Mississippi provide a favourable habitat for M. scandens (Ervin, 2007). M. scandens forms an important component of Florida’s floodplain marshes which are dominated by Salix caroliniana (Lee et al., 2005) and in areas of the Florida Everglades dominated by cattails, Typha domingensis (van der Valk and Rosburg, 1997).

Although it favours riparian habitats and wetlands, a study in Maryland showed that M. scandens did better with limited flooding (Baldwin et al., 2001).

Habitat List

Top of page

Category	Sub-Category	Habitat	Presence	Status
Terrestrial	Managed	Disturbed areas	Secondary/tolerated habitat	Harmful (pest or invasive)
Terrestrial	Managed	Disturbed areas	Secondary/tolerated habitat	Natural
Terrestrial	Natural / Semi-natural	Natural forests	Secondary/tolerated habitat	Natural
Terrestrial	Natural / Semi-natural	Riverbanks	Principal habitat	Natural
Terrestrial	Natural / Semi-natural	Wetlands	Principal habitat	Natural
Terrestrial	Natural / Semi-natural	Scrub / shrublands	Secondary/tolerated habitat	Natural
Littoral		Coastal areas	Secondary/tolerated habitat	Natural
Freshwater		Reservoirs	Secondary/tolerated habitat	Harmful (pest or invasive)
Freshwater		Reservoirs	Secondary/tolerated habitat	Natural
Freshwater		Rivers / streams	Secondary/tolerated habitat	Natural
Freshwater		Ponds	Secondary/tolerated habitat	Natural
Brackish		Estuaries	Secondary/tolerated habitat	Natural
Brackish		Lagoons	Secondary/tolerated habitat	Natural

Biology and Ecology

Top of page

Genetics

Chromosome number 2n=38 (Holm et al., 1991; Flora of North America Editorial Committee, 2013). Tzeng (2003) compared the nrDNA ITS region of M. micrantha, M. cordata and M. scandens, and found a 97% phylogenetic similarity between M. micrantha, while M. scandens was considerably more divergent. Tzeng (2003) utilized plant material of M. micrantha and M. cordata from Taiwan, and used PCR, comparing the ITS sequence of these plants with that available for M. scandens on GeneBank. Few other studies are available on the genetics of M. scandens or other Mikania species. Further research would be useful in resolving the ongoing identity issues (see Identity section).

In a study of the pollen of 10 species of Asteraceae, Mondal et al. (1998) identified the following free amino acids; amino-n-butyric acid, aspartic acid, ornithine, and prolilne in a specimen reputed to be M. scandens.

Reproductive Biology

Borthwick et al. (1950) described M. scandens as an intermediate day plant in terms of flowering response to day-length. There are indications that M. scandens is autogamous (Nauman, 1981).

Seed dispersed may be facilitated by wind or in clothing or hair of animals (PIER, 2013). Seeds are retained in the soil as soil seed banks, although sometimes only a minor constituent of wetland seed bank communities, depending on the environment (Peterson and Baldwin, 2004; Neff et al., 2009). Vegetative reproduction may occur from broken stem fragments. Each node of the stem can produce new roots (PIER, 2013).

Physiology and Phenology

M. scandens exhibited a Type 2 germination response, similar to other related Asteraceae, meaning that the minimum temperature for germination decreases after ripening (Baskin et al., 1993). Neff et al. (2009) observed greater germination of M. scandens under non-flooded versus flooded conditions.

Moon et al. (1993) recorded increased growth rates of M. scandens under flooded conditions when grown in soil collected from the lakeside where it occurred in Florida. Flooded plants increased their aerenchyma tissue, indicating its ability to acclimatize to flooded conditions anatomically to facilitate increased oxygen diffusion to its tissues. The plant appears to utilize stomata located above the waterline to enable submerged parts of the plants to gain a sufficient supply of oxygen.

Longevity

M. scandens is a perennial vine that grows for approximately 20 years (USDA-NRCS, 2013) under favourable conditions.

Activity Patterns

In its native range in eastern North America, M. scandens primarily grows in the summer (USDA-NRCS, 2013).

Population Size and Density

As a vine, M. scandens tends to appear in communities in later successional stages following the initial disturbance, once a substrate is available for its climbing habit. For example, Huffman and Lonard (1983) observed it colonizing swamps in Arkansas in the second stage of succession – the “water-willow herbaceous stage” as the water-willow mat grew in size allowing a variety of marsh plants to invade. As plant communities in the Atchafalaya Delta in Louisiana changed over time with the formation of islands, M. scandens was among species which declined over time, due to changes in water level and loss of vegetation to act as scaffolding for the vines (Shaffer et al., 1992), In a successional sequence involving increasing eutrophication, M. scandens populations is likely to increase over time (Vaithiyanathan and Richardson, 1999).

M. scandens is not an overly strong competitor. It is not generally found in disturbed environments (Weaver, 2009; Anderson et al., 2012) and exhibited higher populations where forests were thinned in Louisiana and Mississippi (McComb and Nobel, 1982).

M. scandens may form substantial seed banks in some areas; e.g., Peterson and Baldwin (2004) found that M. scandens dominated swamp hollows in Maryland and van der Valk and Rosburg (1997) recorded large seed banks (greater than 5000 per square metre) in the cattail zone of the Florida Everglades.

Nutrition

Eutrophic wetlands tend to support more vigorous growth of M. scandens, via higher levels of phosphorus and other nutrients (Vaithiyanathan and Richardson, 1999; King and Richardson, 2007). M. scandens is said to have a medium fertility requirement (USDA-NRCS, 2013).

Associations

M. scandens is colonized by arbuscular mycorrhizal (AM) fungi, as observed in the Florida Everglades (Aziz et al., 1995).

Environmental Requirements

M. scandens prefers fine-medium textured wet soils pH (5.7-8.7) and can withstand some water-logging but has low salinity tolerance (USDA-NRCS, 2013). It requires a minimum frost-free period of 110 days, 75-150 cm of rain; and cannot withstand temperatures below -39ºC (USDA-NRCS, 2013).

Climate

Top of page

Climate	Status	Description
Cf - Warm temperate climate, wet all year	Preferred	Warm average temp. > 10°C, Cold average temp. > 0°C, wet all year
Cs - Warm temperate climate with dry summer	Preferred	Warm average temp. > 10°C, Cold average temp. > 0°C, dry summers
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)
Df - Continental climate, wet all year	Tolerated	Continental climate, wet all year (Warm average temp. > 10°C, coldest month < 0°C, wet all year)

Air Temperature

Top of page

Parameter	Lower limit	Upper limit
Absolute minimum temperature (ºC)	-39
Mean annual temperature (ºC)	10	25
Mean maximum temperature of hottest month (ºC)	15	33
Mean minimum temperature of coldest month (ºC)	-15	20

Rainfall

Top of page

Parameter	Lower limit	Upper limit	Description
Mean annual rainfall	750	1500	mm; lower/upper limits

Soil Tolerances

Top of page

Soil drainage

free
impeded
seasonally waterlogged

Soil reaction

alkaline
neutral

Soil texture

light
medium

Water Tolerances

Top of page

Parameter	Minimum Value	Maximum Value	Typical Value	Status	Life Stage	Notes
Salinity (part per thousand)	0			Optimum		Occurs as an emergent aquatic, near shore
Salinity (part per thousand)	5			Harmful		Occurs as an emergent aquatic, near shore

Natural enemies

Top of page

Natural enemy	Type	Life stages	Specificity
Chauliognathus pennsylvanicus	Herbivore	Plants\|Leaves	not specific
Cosmosoma myrodora	Herbivore	Plants\|Leaves	to genus
Golovinomyces cichoracearum	Pathogen	Plants\|Leaves	not specific
Tylenchulus palustris	Parasite	Plants\|Roots	not specific

Notes on Natural Enemies

Top of page

Dow et al. (1990) found that M. scandens was a host to the nematode Tylenchulus palustris but not T. semipenetrans; both Tylenchulus species are pests of citrus in Florida.

The arctiid moth Cosmosoma myrodora feeds on M. scandens (Hristov and Conner, 2005), as does the soldier beetle, Chauliognathus pennsylvanicus (McLain, 1982).

The powdery mildew, Erysiphe cichoracearum [Golovinomyces cichoracearum] is known to infect M. scandens in the USA (Schmitt, 1955). Evans and Ellison (2005) described a rust species, Puccinia spegazzinii, on M. micrantha and plants identified as M. scandens in the neotropics. However, the voucher specimen identified as M. scandens was M. micrantha as confirmed by molecular analysis of the plant material (Ellison et al., 2004).

Means of Movement and Dispersal

Top of page

M. scandens has some potential for long-distance dispersal, but is less likely to colonize disturbed environments than M. micrantha. The spread of M. scandens is also less likely (Weaver, 2009; Anderson et al., 2012).

Natural Dispersal

Seeds of M. scandens are wind-dispersed as aided by the pappus on the fruit. Vegetative fragments can be carried by water and form new plants through rooting (PIER, 2013).

Vector Transmission

Seeds of M. scandens may adhere to animal fur (PIER, 2013).

Accidental Introduction

Seeds of M. scandens may adhere to clothing, but accidental introductions are more likely to occur through movement of vegetative fragments via machinery, etc.

Intentional Introduction

Species of Mikania may be valued as livestock fodder, ground cover or for medical uses and have been intentionally introduced into new areas for this reason. However, due to the invasive nature of a number of this genus, Mikania propagation tends to be discouraged.

Pathway Causes

Top of page

Cause	Notes	Long Distance	Local	References
Disturbance			Yes	Moon et al. (1993)

Pathway Vectors

Top of page

Vector	Notes	Long Distance	Local	References
Water			Yes	PIER (2013)
Wind			Yes	PIER (2013)

Impact Summary

Top of page

Category	Impact
Cultural/amenity	Positive
Economic/livelihood	Positive
Environment (generally)	Positive and negative
Human health	Positive

Economic Impact

Top of page

Within its native range in eastern North America, M. scandens is rarely seen to have a negative impact, growing primarily in natural areas (Anderson et al., 2012). It is quite common in some areas, particularly in riparian zones and drainage ditches. M. scandens is capable of forming a fairly dense cover, outcompeting other plants through overtopping them and showing a “propensity to become a problematic weed in some areas” (Moon et al., 2003).

Environmental Impact

Top of page

Impact on Habitats

Although M. scandens is fairly common in the southern part of its native range in North America, its weediness is only mentioned with respect to wetlands in Florida, such as the banks of the Oklawaha River (Moon et al., 1993).

Impact on Biodiversity

On Mariana Island, M. scandens is said to be one of the non-native species threatening the endangered plant species, Osmoxylon mariannense (US Fish and Wildlife Service, 2007). With only 10 known individuals of O. mariannense remaining in the wild, “a single adverse environmental events or a decline of successful reproduction in O. mariannense” (US Fish and Wildlife Service, 2007) could have serious consequences, and thus the threat of invasive competitors should be taken seriously. The report does refer to identification of M. scandens by Fosberg (1979), which is prior to when taxonomists began recognizing the confusion between M. scandens and M. micrantha (Parker, 1972), and thus it would be essential to verify the identity of the Mikania species on the island.

Although not noted as of concern, M. scandens has been listed as present in the Pabitora Wildlife Sanctuary, an Indian wildlife tropical grassland reserve where the one-horned rhinoceros occurs (Bairagee and Kalita, 2004). However, due to the location of this record being outside of Northern America, this record must therefore be refering to M. micrantha.

Threatened Species

Top of page

Threatened Species	Conservation Status	Where Threatened	Mechanism	References	Notes
Osmoxylon mariannense	CR (IUCN red list: Critically endangered); USA ESA listing as endangered species		Competition	US Fish and Wildlife Service (2007)

Social Impact

Top of page

The numerous flowers produced by Mikania species are reported as having potential allergenic effects, and produce amino acids that are precursors to allergenic pollen (Mondal et al., 1998).

Risk and Impact Factors

Top of page

Invasiveness

Has a broad native range
Tolerant of shade
Has propagules that can remain viable for more than one year
Reproduces asexually

Impact outcomes

Ecosystem change/ habitat alteration
Host damage
Modification of successional patterns

Impact mechanisms

Allelopathic
Causes allergic responses
Competition - monopolizing resources
Competition - smothering
Pest and disease transmission
Rapid growth
Produces spines, thorns or burrs

Likelihood of entry/control

Difficult to identify/detect as a commodity contaminant

Uses

Top of page

Economic and Social Benefits

There are many published reports of medicinal uses of M. scandens around the world, but most of these are from outside North America, and thus the plants in question represent M. micrantha (see Identity section).

The plant identified as M. scandens in India and Bangladesh is utilized in that region for a variety of medical purposes, including use in folk medicine for the treatment of stomach ulcers (Herz et al., 1970; Hasan et al., 2009; Chandra et al., 2012). In a survey of villagers in the Eastern Himalayan zone of Arunachal Pradesh, India, M. scandens was cited as the most popular treatment for diarrhoea; villagers also used it as a blood coagulant (Tangjang et al., 2011). In Madagascar a cold tea from M. scandens has been used as a wash to treat scabies (Novy, 1997).

In vitro experiments showed that the flowers displayed marked anti-inflammatory properties (Chandra et al., 2012). Rural dwellers in India also utilize young Mikania leaves for management of insect bites and stings, and research has confirmed analgesic and in vitro antioxidant and antidiabetic activities of leaf material (Hasan et al., 2009; Pal, 2013). The antioxidants exhibit potential to treat diseases involving oxidants or free radicals. Dey et al. (2011b) reported that root extracts had more potent anti-inflammatory potential than aerial parts of the plant. Plant extracts were also shown to have locomotor depressant, muscle relaxant and sedative neuropharmacological properties (Dey et al., 2011a; 2012c). Another study found that an extract from M. scandens collected in India had potent liver protective activity (Maity and Ahmad, 2012).

Compounds from Mikania species are also used as antimicrobial folk medicines in the new world; the compound deoxymikanolide was identified as the principle active ingredient from M. micrantha (Lentz et al., 1998) and Radtke and König (2008) demonstrated antimicrobial activity from foliage. Deoxymikanolide was originally described from M. scandens (Herz et al., 1970), but this was clearly a misidentification (Lentz et al., 1998).

Baidya et al. (1995) found that in India, the Mikania they tested provided quality forage for goats or cattle. It was relatively rich in crude protein (17%), provided a reasonable source of other nutrients and produced soft, fairly palatable leaves. Baidya et al. (1995) described M. scandens as a common plant in marshy areas or road-sides, and distributed throughout Eastern Assam and South India (according to Singh et al., 1990); this is therefore referring to M. micrantha and not M. scandens (see Identity section).

Dey et al. (2012a; 2012b) showed that phytochemicals from both aerial parts and roots of the plant identified in India as M. scandens had considerable allelopathic potential, inhibiting both seed germination and radicle growth of Cicer arietinum and Triticum aestivum. Likewise, Piyasena and Dharmatne (2013), utilizing material referred to as M. scandens from Sri Lanka, found that aerial parts of the plant strongly inhibited seed germination via the compound mikanolide.

Environmental Services

M. scandens was listed as one of the plants involved in the recovery of a marsh community in Connecticut, USA after removal of invasive Phragmites australis (Farnsworth and Meyerson, 1999). In a habitat in Florida, host to the extinct dusky seaside sparrow (Ammodramus maritimus nigrescens), M. scandens is one of the constituents of the plant community (Holder et al., 1980). M scandens was also among the target plants for restoration of a wetland important for wildlife in the Florida Everglades (Smith et al., 2002) where it thrives in cattail (Typha domingensis) dominated zones (van der Valk and Rosburg, 1997). In some areas Mikania species may provide a nutritional food source for herbivorous mammals (Mondal et al., 2003; Matsubayashi et al., 2007).

Uses List

Top of page

Animal feed, fodder, forage

Fodder/animal feed

Environmental

Revegetation
Wildlife habitat

Human food and beverage

Leaves (for beverage)

Materials

Chemicals

Medicinal, pharmaceutical

Source of medicine/pharmaceutical
Traditional/folklore

Similarities to Other Species/Conditions

Top of page

Floral characters are often instrumental in differentiating different species of Mikania (Anderson et al., 2012). The following characteristics may be used to distinguish them (Choudhury, 1972; Holm et al., 1977):

M. micrantha: pappus bristles 32-38, white, corolla white, head length 4.5-6 mm, nodal appendages membranous.

M. cordata: pappus bristles 40-45, reddish, corolla white, head length 7-7.5 mm, nodal appendages form furry ridges not membranous.

M. scandens: pappus bristles 30-35, usually whitish, corolla pale purple, head length 5-7 mm.

Furthermore, the inflorescence of M. scandens is denser than that of M. micrantha, with round-topped corymbs (as compared to the looser, more paniculate inflorescence of M. micrantha). The purple corolla often seen in M. scandens is never observed in M. micrantha. The leaves of M. scandens are characteristically more sharply angled and triangular-sagittate or triangular-hastate as compared to the more oval, cordate and crenate leaves of M. micrantha (Holm et al., 1997).

Distributional differences are also important (Robinson, 1934; Parker, 1972; Holmes, 1975). Although M. micrantha is native to tropical America, it was introduced widely in Southeast Asia, where M. cordata is also native, as well as Africa. M. scandens is native to eastern North America, and although reported outside this range, there has been limited verification of these reports (Parker, 1972).

The range of M. scandens overlaps with that of M. micrantha in Florida, where efforts are being made to help managers identify the Mikania species correctly (Anderson et al., 2012). In Florida M. scandens is relatively common and widespread, M. cordifolia is prevalent in the central and southern peninsula, while M. micrantha forms local infestations (Manrique et al., 2011; Anderson et al., 2012).

Useful characteristics for distinguishing M. micrantha from M. scandens include: leaf colour and shape, stem colour, growth habit, and the pseudostipules between the petiole bases of the leaves (Holmes, 1993; Anderson et al., 2012).

Prevention and Control

Top 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.

Prevention

Avoiding excessive disturbance around waterways in areas vulnerable to invasion of M. scandens, (Moon et al., 1993), should prevent establishment of new populations.

Control

Control methods utilized for M. micrantha should also be effective for M. scandens. Herbicidal control methods may be somewhat limited by the occurrence of M. scandens in or near wetland areas.

Cultural Control and Sanitary Measures

Although excessive flooding does not promote growth of M. scandens (Baldwin et al., 2001), M. scandens has been shown to be flood resistant. Therefore, cultural measures to reduce the growth of M. scandens should be carried out in such a way to avoid its adaptive response to flooding (Moon et al., 1993).

Physical/Mechanical Control

Physical/mechanical control of M. scandens can be difficult due to the extensive growth of vines and their ability to propagate from fragments.

Biological Control

There have been some reports of efforts to control M. scandens by classical biological control using the thrips, Liothrips mikaniae from Trinidad (Waterhouse and Norris, 1987). However, due to the location of these releases (outside of North America)and the distribution of M. scandens, it is likely that M. micrantha was the actual target.

It may be possible to manage Mikania species in some areas through livestock grazing.

Chemical Control

Control by herbicides such as glyphosate, 2,4-D or paraquat has been shown to be effective against Mikania species, but re-growth is possible after herbicide applications.

Gaps in Knowledge/Research Needs

Top of page

There is a need for plant taxonomists to check herbarium specimens and photos from geographic regions around the world where putatively M. scandens occurs outside its native range in eastern North America, i.e., to examine specimens from south-east Asia and the Pacific Islands to verify what species of Mikania occurs in these areas. Furthermore, the work of Tzeng (2003) comparing the nrDNA ITS region among Mikania species showing a strong divergence between M. micrantha and M. scandens could be replicated using putative M. scandens material from various accessions.

References

Top of page

Alvarez-Aquino C; Williams-Linera G; Newton AC, 2005. Disturbance effects on the seed bank of Mexican cloud forest fragments. Biotropica, 37(3):337-342.

Anderson PJ; Weaver Jr RE; Neubig KM; Franks MS; Dixon WN, 2012. Which Mikania: native vine or noxious weed?, 37. Flordia, USA: Florida Department of Agriculture and Consumer Services. http://www.freshfromflorida.com/content/download/9956/136004/botcirc37

Anderson RR; Brown RG; Rappleye RD, 1968. Water quality and plant distribution along the Upper Patuxent River, Maryland. Chesapeake Science, 9(3):145-156.

Aziz T; Sylvia DM; Doren RF, 1995. Activity and species composition of arbuscular mycorrhizal fungi following soil removal. Ecological Applications, 5(3):776-784.

Bacone JA; Hedge CL, 1979. A preliminary list of endangered and threatened vascular plants in Indiana. Proceedings of the Indiana Academy of Science, 89:359-371.

Baidya N; Mandal L; Banerjee GC, 1995. Nutritive values of Mikania scandens and Erythrina indica in Black Bengal goats. Small Ruminant Research, 18(2):185-187.

Bairagee A; Kalita J, 2004. Imperata cylindrical (Linn.) Raeusch in the grasslands of Pabitora Wildlife Sanctuary, Assam, India. Zoos' Print Journal, 19(4):1432-1434.

Baldwin AH; Egnotovich MS; Clarke E, 2001. Hydrologic change and vegetation of tidal freshwater marshes: field, greenhouse, and seed-bank experiments. Wetlands, 21(4):519-531.

Banerjee A; Matai S, 1990. Composition of Indian aquatic plants in relation to utilization as animal forage. Journal of Aquatic Plant Management, 28:69-73.

Barreto RW; Evans HC, 1995. The mycobiota of the weed Mikania micrantha in southern Brazil with particular reference to fungal pathogens for biological control. Mycological Research, 99(3):343-352

Baskin CC; Baskin JM; Leck MA, 1993. Afterripening pattern during cold stratification of achenes of ten perennial Asteraceae from Eastern North America, and evolutionary implication. Plant Species Biology, 8(1):61-65.

Borthwick HA; Parker MW; Hendricks SB, 1950. Recent developments in the control of flowering by photoperiod. The American Naturalist, 84:117-134.

Brouillet L; Coursol F; Favreau M, 2006. VASCAN. The database of Canadian vascular plants. VASCAN. The database of Canadian vascular plants. Herbier Marie-Victorin, Montréal, Canada: Institut de recherche en biologie végétale, Université de Montréal, unpaginated.

Chandra S; Dey P; Bhattacharya S, 2012. Preliminary in vitro assessment of anti-inflammatory property of Mikania scandens flower extract. Journal of Advanced Pharmacy Education & Research, 2(1):25-31.

Choudhury AK, 1972. Controversia Mikania (climber) - a threat to the forests and agriculture. Indian Forester, 98:178-186.

Cock MJW, 1982. Potential biological control agents for Mikania micrantha H. from the Neotropical region. Tropical Pest Management, 28:242-254.

Dey P; Chandra S; Chatterjee P; Bhattacharya S, 2011. Neuropharmacological properties of Mikania scandens (L.) Willd. (Asteraceae). Journal of Advanced Pharmaceutical Technology & Research, 2:255-259.

Dey P; Chandra S; Chatterjee P; Bhattacharya S, 2012. Allelopathic potential of aerial parts from Mikania scandens (L.) Willd. World Journal of Agricultural Sciences, 8(2):203-207.

Dey P; Chandra S; Chatterjee P; Bhattacharya S, 2012. Assessment of allelopathic property of Mikania scandens root. Current Trends in Biotechnology and Pharmacy, 6(3):322-327.

Dey P; Chandra S; Chatterjee P; Bhattacharya S, 2012. Neuropharmocological activities of Mikania scandens root. Global Journal of Pharmacology, 6(3):193-198.

Dey P; Chatterjee P; Chandra S; Bhattacharya S, 2011. Comparative in vitro evaluation of anti-inflammatory effects of aerial parts and roots from Mikania scandens. Journal of Advanced Pharmacy Education & Research, 1(6):271-277.

Dow RL; Inserra RN; Esser RP; Langdon KR, 1990. Distribution, hosts, and morphological characteristics of Tylenchulus palustris in Florida and Bermuda. Journal of Nematology, 22(4S):724-728.

Ellison CA; Evans HC; Ineson J, 2004. The significance of intraspecific pathogenicity in the selection of a rust pathotype for the classical biological control of Mikania micrantha (mile-a-minute weed) in Southeast Asia. In: Proceedings of the 11th International Symposium on Biological Control of Weeds [ed. by Cullen, J. M. \Briese, D. T. \Kriticos, D. J. \Lonsdale, W. M. \Morin, L. \Scott, J. K.]. Canberra, Australia: CSIRO Entomology, 102-107.

Ervin GN, 2007. An experimental study on the facilitative effects of tussock structure among wetland plants. Wetlands, 27(3):620-630.

Evans HC; Ellison CA, 2005. The biology and taxonomy of rust fungi associated with the neotropical vine Mikania micrantha, a major invasive weed in Asia. Mycologia, 97(4):935-947.

Farnsworth EJ; Meyerson LA, 1999. Species composition and inter-annual dynamics of a freshwater tidal plant community following removal of the invasive grass, Phragmites australis. Biological Invasions, 1:115-127.

Fish and Wildlife Service US, 2004. Endangered and threatened wildlife and plants; determination of endangered status and prudency determination for designation of critical habitat for two plant species from the CNMI. Federal Register, 69(68)., USA: US Fish and Wildlife Service, 18499-18507.

Flora of North America Editorial Committee, 2013. Flora of North America North of Mexico. Flora of North America. St. Louis, Missouri and Cambridge, Massachusetts, USA: Missouri Botanical Garden and Harvard University Herbaria. http://www.efloras.org/flora_page.aspx?flora_id=1

Fosberg FR; Sachet MH; Oliver R, 1979. A geographical checklist of the Micronesian Dicotyledonae. Micronesica, 15:1-295.

Ghani A, 2003. Asiatic Society of Bangladesh, 2. Dhaka, Bangladesh 603 pp.

Gough L; Grace JB, 1994. The influence of vines on an oligohaline marsh community: results of a removal and fertilization study. Oecologia, 112:403-411.

Gough L; Grace JB; Taylor KL, 1994. The relationship between species richness and community biomass: the importance of environmental variables. Oikos, 70(2):271-279.

Harvill AM Jr, 1965. The vegetation of Parramore Island, Virginia. Castanea, 30(4):226-228.

Hasan SMR; Mariam Jamila; Majumder MM; Raushanara Akter; Hossain MM; Mazumder MEH; Alam MA; Rumana Jahangir; Rana MS; Arif M; Rahman S, 2009. Analgesic and antioxidant activity of the hydromethanolic extract of Mikania scandens (L.) Willd. leaves. American Journal of Pharmacology and Toxicology, 4(1):1-7.

Herz W; Subramaniam PS; Santhanam PS; Aota K; Hall AL, 1970. Structure elucidation of sesquiterpene dilactones from Mikania scandens (L.) Willd. The Journal of Organic Chemistry, 35(5):1453-1464.

Holder GL; Johnson MK; James JL, 1980. Cattle grazing and management of dusky seaside sparrow habitat. Wildlife Society Bulletin, 8(2):105-109.

Holm LG; Plucknett DC; Pancho JV; Herberger JP, 1991. The world’s worst weeds: distribution and biology. Florida, USA: Krieger Publishing Company, USA.

Holmes WC, 1975. A revision of Mikania scandens and relatives (Compositae). Mississippi, USA: Mississippi State University.

Holmes WC, 1993. The genus Mikania (Compositae: Eupatorieae) in the Greater Antilles. Texas, USA: Botanical Research Institute of Texas, 69 pp.

Hristov N; Conner WE, 2005. Effectiveness of tiger moth (Lepidoptera, Artiidae) chemical defenses against an insectivorous bat (Eptesicus fuscus). Chemoecology, 15:105-113.

Huffman RT; Lonard RI, 1983. Successional patterns on floating vegetation mats in a southwestern Arkansas bald cypress swamp. Castanea, 48(2):73-78.

Hunt KW, 1943. Floating mats on a southeastern coastal plain reservoir. Bulletin of the Torrey Botanical Club, 70:481-8.

Josekutty PC; Wakuk EE; Joseph MJ, 2002. Invasive weedy angiosperms in Kosrae, Federated States of Micronesia. Micronesica Supplement, 6:61-65. [Invasive species and their management.]

King RM; Robinson H, 1987. The genera of the Eupatorieae (Asteraceae). Systematic Botany, 14(2):263-266.

King RS; Richardson CJ, 2007. Subsidy-stress response of macroinvertebrate community biomass to a phosphorus gradient in an oligotrophic wetland ecosystem. Journal of the North American Benthological Society, 26(3):491-508.

Lee MAB; Snyder KL; Valentine-Darby P; Miller SJ; Ponzio KJ, 2005. Dormant season prescribed fire as a management tool for the control of Salix caroliniana Michx. in a floodplain marsh. Wetlands Ecology and Management, 13(4):479-487.

Lentz DL; Clark AM; Hufford CD; Meurer-Grimes B; Passreiter CM; Cordero J; Ibrahimi O; Okunade AL, 1998. Antimicrobial properties of Honduran medicinal plants. Journal of Ethnopharmacology, 63(3):253-263.

MacKee HS, 1994. Catalogue of introduced and cultivated plants in New Caledonia. (Catalogue des plantes introduites et cultivées en Nouvelle-Calédonie.) Paris, France: Muséum National d'Histoire Naturelle, unpaginated.

Maity T; Ahmad A, 2012. Protective effect of Mikania scandens (L.) Willd. against isoniazid induced hepatotoxicity in rats. International Journal of Pharamcy and Pharmaceutical Sciences, 4:466-469.

Manrique V; Diaz R; Cuda JP; Overholt WA, 2011. Suitability of a new plant invader as a target for biological control in Florida. Invasive Plant Science and Management, 4(1):1-10.

Mathies PS; Holmes WC; Allen AS, 1983. The vascular flora of Cunningham Brake, a cypress-gum swamp in Natchitoches Parish, Louisiana. Castanea, 48(1):24-31.

Matsubayashi H; Lagan P; Majalap N; Tangah J; AbdSukor JR; Kitayama K, 2007. Importance of natural licks for the mammals in Bornean inland tropical rain forests. Ecological Research, 22(5):742-748. http://www.springerlink.com/link.asp?id=112404

McComb WC; Noble RE, 1982. Response of understory vegetation to improvement cutting and physiographic site in two mid-south forest stands. Castana, 47(1):60-77.

McLain DK, 1982. Density dependent sexual selection and positive phenotypic assortative mating in natural populations of the soldier beetle, Chauliognathus pennsylvanicus. Evolution, 36(6):1227-1235.

Merrill ED, 1925. An enumeration of Philippine flowering plants. Manila, Philippines: Bureau of Printing.

Mondal AK; Sanjukta Parui; Sudhendu Mandal, 1998. Analysis of the free amino acid content in pollen of nine Asteraceae species of known allergenic activity. Annals of Agricultural and Environmental Medicine, 5(1):17-20.

Mondal P; Biswas P; Rajendran D, 2003. Micronutrient status of soil, plant and dairy cattle in coastal saline zone of West Bengal. Indian Journal of Animal Sciences, 73(9):1077-1080.

Moon M; Rattray MR; Putz FE; Bowes G, 1993. Acclimatization to flooding of the herbaceous vine, Mikania scandens. Functional Ecology, 7(5):610-615.

Muniappan R; Cruz J; Bamba J, 2002. Invasive plants and their control in Micronesia. Micronesica Supplement, 6:85-92.

Nauman CE, 1981. A re-examination of Mikania Willd. (Compositae) in Florida. Bulletin of the Torrey Botanical Club, 108(4):467-471.

Neff KP; Rusello K; Baldwin AH, 2009. Rapid seed bank development in restored tidal freshwater wetlands. Restoration Ecology, 17(4):539-548.

Novy JW, 1997. Medicinal plants of the eastern region of Madagascar. Journal of Ethnopharmacology, 55(2):119-126.

Pal D, 2013. Comparative analysis of in vitro antioxidant activity of two selected plants with a reference to antidiabetic profile. Asian Journal of Chemistry, 25(4):2165-2169.

Pal RK; Das KK, 2001. Record of new host plants of Bihar hairy caterpillar Spilosoma oblique Wlk. at Murshidabad district of West Bengal. Environment and Ecology, 19(2):489-490.

Parker C, 1972. The Mikania problem. PANS, 18(3):312-315.

Peekel PG, 1984. Flora of the Bismarck Archipelago for naturalists [ed. by Henty, E. E.]. Lae, Papua New Guinea: Office of Forests, Division of Botany, 638 pp.

Peterson JE; Baldwin AH, 2004. Variation in wetland seed banks across a tidal freshwater landscape. American Journal of Botany, 91(8):1251-1259.

PIER, 2013. Pacific Islands Ecosystems at Risk. Honolulu, Hawaii, USA: HEAR, University of Hawaii. http://www.hear.org/pier/index.html

Piyasena KGNP; Dharmaratne HRW, 2013. Allelopathic activity studies of Mikania scandens. Natural Product Research, 27(1):76-79.

Pratiwi NM, 1989. Identification of important weeds in some industrial forest plantations at Benakat, South Sumatra. Buletin Penelitian Hutan, 519:56-67.

Radtke OA; König W, 2008. Leaf and cortex extracts of Mikania scandens (Asteraceae) exhibit cytotoxic effects against Spironucleus meleagridis trophozoites from turkey-cock and antibacterial properties. Planta Medica, 74(9):941.

Raulerson L, 2006. Checklist of Plants of the Mariana Islands. University of Guam Herbarium Contribution, 37. 1-69.

Robinson BL, 1934. The variability of two wide-ranging species of Mikania. Contributions from the Gray Herbarium of Harvard University. 49-55. http://www.jstor.org/stable/41764220

Schmitt JA, 1955. The host specialization of Erysiphe cichoracearum from Zinnia, Phlox, and cucurbits. Mycologia, 47(5):688-701 pp.

Scoogan HJ, 1979. The flora of Canada. Ottawa, Canada: Canada Science & Technology Museum, 3799 pp.

Shaffer GP; Sasser CE; Gosselink JG; Rejmánek M, 1992. Vegetation dynamics in the emerging Atchafalaya Delta, Louisiana, USA. Journal of Ecology (Oxford), 80(4):677-687.

Singh U; Wadhwani AM; Johri BM, 1990. Dictionary of Economic Plants in India. New Delhi, India: Indian Council of Agricultural Research, 288 pp.

Smith SM; McCormick PV; Leeds JA; Garrett PB, 2002. Constraints of seed bank species composition and water depth for restoring vegetation in the Florida Everglades, U.S.A. Restoration Ecology, 10(1):138-145.

Stone BC, 1970. The flora of Guam. Micronesica, 6:659 pp.

Tangjang SNamsa ND; Aran C; Litin A, 2011. An ethnobotanical survey of medicinal plants in the Eastern Himalayan zone of Arunachal Pradesh, India. Journal of Ethnopharmacology, 134(1):18-25.

Tripathi RS; Khan ML; Yadav AS, 2012. Biology of Mikania micrantha H.: a review. In: Invasive alien plants: an ecological appraisal for the Indian subcontinent [ed. by Bhatt, J. R.\Singh, J. S.\Singh, S. P.\Tripathi, R. S.\Kohli, R. K.]. Wallingford, UK: CABI, 99-107.

Tzeng GY, 2003. Population genetic variation of Mikania species in Taiwan Masters Thesis, Taiwan: National Sun Yet-sen Univeristy, 70 pp. http://etd.lib.nsysu.edu.tw/ETD-db/ETD-search/view_etd?URN=etd-0804103-154817

Uddin MB; Steinbauer MJ; Jentsch A; Mukul SA; Beierkuhnlein C, 2013. Do environmental attributes, disturbances and protection regimes determine the distribution of exotic plant species in Bangladesh forest ecosystem? Forest Ecology and Management, 303:72-80.

US Fish and Wildlife Service, 2007. Recovery Plan for Two Plants from Rota (Nesogenes rotensis and Osmoxylon mariannense). Recovery Plan for Two Plants from Rota (Nesogenes rotensis and Osmoxylon mariannense). Portland, Oregon, USA: US Fish and Wildlife Service, 86 pp.

USDA-ARS, 2013. 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, 2013. The PLANTS Database. Baton Rouge, USA: National Plant Data Center. http://plants.usda.gov/

Vaithiyanathan P; Richardson CJ, 1999. Macrophyte species changes in the Everglades: examination along a eutrophic gradient. Journal of Environmental Quality, 28:1347-1358.

Valk AG van der; Rosburg TR, 1997. Seed bank composition along a phosphorus gradient in the northern Florida Everglades. Wetlands, 17(2):228-236.

Waterhouse DF, 1994. Biological Control of Weeds: Southeast Asian Prospects. Canberra, Australia: ACIAR Monograph No 26.

Waterhouse DF; Norris KR, 1987. Biological control: Pacific prospects. viii + 454pp

Weaver R, 2009. The mile-a-minute (Mikania micrantha). Florida Department of Agriculture and Consumer Services Division of Plant Industry, 2 pp. http://www.freshfromflorida.com/content/download/9959/136022/weaver-mikania-micrantha-report-121109.pdf

Whistler WA, 1996. Botanical survey of Diego Garcia, Chagos Archipelago, British Indian Ocean Territory. Isle Botanica. http://www.zianet.com/tedmorris/dg/2005nrmp-appendixe-botanicalsurvey.pdf

White DA, 1983. Plant communities of the Lower Pearl River Basin, Louisiana. American Midland Naturalist, 110(2):381-396.

Whittle AM, 1996. Mikania scandens - a new record? Quarterly Newsletter - Tea Research Foundation of Central Africa, No. 122:20-22.

Zhang LY; Ye WH; Cao HL; Feng HL, 2004. Mikania micrantha H. in China - an overview. Weed Research, 44:42-49.

Distribution References

Brouillet L, Coursol F, Favreau M, 2006. Bunias orientalis. In: VASCAN. The database of Canadian vascular plants, Herbier Marie-Victorin, Montréal, Canada: Institut de recherche en biologie végétale, Université de Montréal. unpaginated.

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

Diaz R, Romero S, Roda A, Mannion C, Overholt W A, 2015. Diversity of arthropods associated with Mikania spp. and Chromolaena odorata (Asterales: Asteraceae: Eupatorieae) in Florida. Florida Entomologist. 98 (1), 389-393. DOI:10.1653/024.098.0168

Fosberg F R, Sachet M H, Oliver R, 1979. A geographical checklist of the Micronesian dicotyledonae. Micronesica. 1-295.

Ghani A, 2003. Asiatic Society of Bangladesh., 2 Dhaka, Bangladesh: 603 pp.

MacKee H S, 1994. Catalogue des plantes introduites et cultivées en Nouvelle-Calédonie. Paris, France: Muséum National d'Histoire Naturelle. unpaginated.

Matsubayashi H, Lagan P, Majalap N, Tangah J, Abd Sukor J R, Kitayama K, 2007. Importance of natural licks for the mammals in Bornean inland tropical rain forests. Ecological Research. 22 (5), 742-748. http://www.springerlink.com/link.asp?id=112404 DOI:10.1007/s11284-006-0313-4

Novy J W, 1997. Medicinal plants of the eastern region of Madagascar. Journal of Ethnopharmacology. 55 (2), 119-126. DOI:10.1016/S0378-8741(96)01489-4

Peekel PG, 1984. Flora of the Bismarck Archipelago for naturalists., [ed. by Henty EE]. Lae, Papua New Guinea: Office of Forests, Division of Botany. 638 pp.

Piyasena K G N P, Dharmaratne H R W, 2013. Allelopathic activity studies of Mikania scandens. Natural Product Research. 27 (1), 76-79. http://www.tandfonline.com/loi/gnpl20 DOI:10.1080/14786419.2012.656110

Pratiwi, Nazif M, 1989. Identification of important weeds in some industrial forest plantations at Benakat, South Sumatra. (Pengenalan jenis gulma penting pada hutan tanaman industri (HTI) di Benakat, Sumatera Selatan.). Buletin Penelitian Hutan. 55-67.

Raulerson L, 2006. Checklist of Plants of the Mariana Islands. In: University of Guam Herbarium Contribution, 37 1-69.

Singh U, Wadhwani AM, Johri BM, 1990. Dictionary of Economic Plants in India., New Delhi, India: Indian Council of Agricultural Research. 288 pp.

Stone B C, 1970. The flora of Guam. A manual for the identification of the vascular plants of the island. Guam: University of Guam. vi + 659 pp.

Uddin M B, Steinbauer M J, Jentsch A, Mukul S A, Beierkuhnlein C, 2013. Do environmental attributes, disturbances and protection regimes determine the distribution of exotic plant species in Bangladesh forest ecosystem? Forest Ecology and Management. 72-80. http://www.sciencedirect.com/science/article/pii/S0378112713002077 DOI:10.1016/j.foreco.2013.03.052

USDA-ARS, 2013. Germplasm Resources Information Network (GRIN). Online Database. Beltsville, Maryland, USA: National Germplasm Resources Laboratory. https://npgsweb.ars-grin.gov/gringlobal/taxon/taxonomysimple.aspx

USDA-NRCS, 2013. The PLANTS Database. Greensboro, North Carolina, USA: National Plant Data Team. https://plants.sc.egov.usda.gov

Whistler WA, 1996. Botanical survey of Diego Garcia, Chagos Archipelago, British Indian Ocean Territory. In: Isle Botanica, 49 pp. http://www.zianet.com/tedmorris/dg/2005NRMP-Appendixe-botanicalsurvey.pdf

Whittle A M, 1996. Mikania scandens - a new record? Quarterly Newsletter - Tea Research Foundation of Central Africa. 20-22.

Contributors

Top of page

21/12/2013 Original text by:

David R. Clements, Trinity Western University, Canada

Distribution Maps

Top of page

You can pan and zoom the map

Save map

Unsupported Web Browser:

One or more of the features that are needed to show you the maps functionality are not available in the web browser that you are using.

Please consider upgrading your browser to the latest version or installing a new browser.

More information about modern web browsers can be found at http://browsehappy.com/

Datasheet

Mikania scandens

Toolbox