dcsimg
Image of alligator weed
Creatures » » Plants » » Dicotyledons » » Amaranth Family »

Alligator Weed

Alternanthera philoxeroides (Mart.) Griseb.

Comments

provided by eFloras
Alternanthera philoxerioides is said to reproduce only vegetatively in North America. I have seen no fruit or seed.
license
cc-by-nc-sa-3.0
copyright
Missouri Botanical Garden, 4344 Shaw Boulevard, St. Louis, MO, 63110 USA
bibliographic citation
Flora of North America Vol. 4: 448, 449 in eFloras.org, Missouri Botanical Garden. Accessed Nov 12, 2008.
source
Flora of North America @ eFloras.org
editor
Flora of North America Editorial Committee
project
eFloras.org
original
visit source
partner site
eFloras

Description

provided by eFloras
Herbs, perennial, aquatic to semiterrestrial, stoloniferous, to 50 dm. Stems prostrate, forming mats, often fistulose, glabrous. Leaves sessile; blade narrowly elliptic, elliptic, or oblanceolate, 3.5-7.1 × 0.5-2 cm, herbaceous, apex acute to obtuse, glabrous. Inflorescences terminal and axillary, pedunculate; heads white, globose, 1.4-1.7 cm diam.; bracts not keeled, less than 1/2 as long as tepals. Flowers: tepals monomorphic, white, lanceolate or oblong, 6 mm, apex acute, glabrous; stamens 5; pseudostaminodes ligulate. Utricles not seen. Seeds not seen.
license
cc-by-nc-sa-3.0
copyright
Missouri Botanical Garden, 4344 Shaw Boulevard, St. Louis, MO, 63110 USA
bibliographic citation
Flora of North America Vol. 4: 448, 449 in eFloras.org, Missouri Botanical Garden. Accessed Nov 12, 2008.
source
Flora of North America @ eFloras.org
editor
Flora of North America Editorial Committee
project
eFloras.org
original
visit source
partner site
eFloras

Description

provided by eFloras
Herbs perennial. Stem ascending from a creeping base, 55-120 cm, branched; young stem and leaf axil white hairy; old ones glabrous. Petiole 3-10 mm, glabrous or slightly hairy; leaf blade oblong, oblong-obovate, or ovate-lanceolate, 2.5-5 × 0.7-2 cm, glabrous or ciliate, adaxially muricate, base attenuate, margin entire, apex acute or obtuse, with a mucro. Heads with a peduncle, solitary at leaf axil, globose, 0.8-1.5 cm in diam. Bracts and bracteoles white, 1-veined, apex acuminate; bracts ovate, 2-2.5 mm; bracteoles lanceolate, ca. 2 mm. Tepals white, shiny, oblong, 5-6 mm, glabrous, apex acute. Filaments 2.5-3 mm, connate into a cup at base; pseudostaminodes oblong-linear, ca. as long as stamens. Ovary obovoid, compressed, with short stalk. Fruit not known. Fl. May-Oct. 2n = 100*.
license
cc-by-nc-sa-3.0
copyright
Missouri Botanical Garden, 4344 Shaw Boulevard, St. Louis, MO, 63110 USA
bibliographic citation
Flora of China Vol. 5: 427 in eFloras.org, Missouri Botanical Garden. Accessed Nov 12, 2008.
source
Flora of China @ eFloras.org
editor
Wu Zhengyi, Peter H. Raven & Hong Deyuan
project
eFloras.org
original
visit source
partner site
eFloras

Distribution

provided by eFloras
E Nepal: Native of Brazil, introduced in many tropical countries.
license
cc-by-nc-sa-3.0
copyright
Missouri Botanical Garden, 4344 Shaw Boulevard, St. Louis, MO, 63110 USA
bibliographic citation
Annotated Checklist of the Flowering Plants of Nepal Vol. 0 in eFloras.org, Missouri Botanical Garden. Accessed Nov 12, 2008.
source
Annotated Checklist of the Flowering Plants of Nepal @ eFloras.org
author
K.K. Shrestha, J.R. Press and D.A. Sutton
project
eFloras.org
original
visit source
partner site
eFloras

Distribution

provided by eFloras
introduced; Ala., Ark., Calif., Fla., Ga., Ill., Ky., La., Miss., N.C., S.C., Tenn., Tex., Va.; West Indies; native to South America.
license
cc-by-nc-sa-3.0
copyright
Missouri Botanical Garden, 4344 Shaw Boulevard, St. Louis, MO, 63110 USA
bibliographic citation
Flora of North America Vol. 4: 448, 449 in eFloras.org, Missouri Botanical Garden. Accessed Nov 12, 2008.
source
Flora of North America @ eFloras.org
editor
Flora of North America Editorial Committee
project
eFloras.org
original
visit source
partner site
eFloras

Elevation Range

provided by eFloras
100-200 m
license
cc-by-nc-sa-3.0
copyright
Missouri Botanical Garden, 4344 Shaw Boulevard, St. Louis, MO, 63110 USA
bibliographic citation
Annotated Checklist of the Flowering Plants of Nepal Vol. 0 in eFloras.org, Missouri Botanical Garden. Accessed Nov 12, 2008.
source
Annotated Checklist of the Flowering Plants of Nepal @ eFloras.org
author
K.K. Shrestha, J.R. Press and D.A. Sutton
project
eFloras.org
original
visit source
partner site
eFloras

Flowering/Fruiting

provided by eFloras
Flowering early spring-summer.
license
cc-by-nc-sa-3.0
copyright
Missouri Botanical Garden, 4344 Shaw Boulevard, St. Louis, MO, 63110 USA
bibliographic citation
Flora of North America Vol. 4: 448, 449 in eFloras.org, Missouri Botanical Garden. Accessed Nov 12, 2008.
source
Flora of North America @ eFloras.org
editor
Flora of North America Editorial Committee
project
eFloras.org
original
visit source
partner site
eFloras

Habitat

provided by eFloras
Herbs
license
cc-by-nc-sa-3.0
copyright
Missouri Botanical Garden, 4344 Shaw Boulevard, St. Louis, MO, 63110 USA
bibliographic citation
Annotated Checklist of the Flowering Plants of Nepal Vol. 0 in eFloras.org, Missouri Botanical Garden. Accessed Nov 12, 2008.
source
Annotated Checklist of the Flowering Plants of Nepal @ eFloras.org
author
K.K. Shrestha, J.R. Press and D.A. Sutton
project
eFloras.org
original
visit source
partner site
eFloras

Habitat

provided by eFloras
Ponds, ditches, streams, bayous; 0-200m.
license
cc-by-nc-sa-3.0
copyright
Missouri Botanical Garden, 4344 Shaw Boulevard, St. Louis, MO, 63110 USA
bibliographic citation
Flora of North America Vol. 4: 448, 449 in eFloras.org, Missouri Botanical Garden. Accessed Nov 12, 2008.
source
Flora of North America @ eFloras.org
editor
Flora of North America Editorial Committee
project
eFloras.org
original
visit source
partner site
eFloras

Habitat & Distribution

provided by eFloras
Cultivated, waste places. Beijing, Fujian, Guangxi, Hebei, Hubei, Hunan, Jiangsu, Jiangxi, Sichuan, Taiwan, Zhejiang [native to South America (Brazil)].
license
cc-by-nc-sa-3.0
copyright
Missouri Botanical Garden, 4344 Shaw Boulevard, St. Louis, MO, 63110 USA
bibliographic citation
Flora of China Vol. 5: 427 in eFloras.org, Missouri Botanical Garden. Accessed Nov 12, 2008.
source
Flora of China @ eFloras.org
editor
Wu Zhengyi, Peter H. Raven & Hong Deyuan
project
eFloras.org
original
visit source
partner site
eFloras

Synonym

provided by eFloras
Bucholzia philoxeroides Martius, Beitr. Amarantac., 107. 1825; Achyranthes philoxeroides (Martius) Standley
license
cc-by-nc-sa-3.0
copyright
Missouri Botanical Garden, 4344 Shaw Boulevard, St. Louis, MO, 63110 USA
bibliographic citation
Flora of North America Vol. 4: 448, 449 in eFloras.org, Missouri Botanical Garden. Accessed Nov 12, 2008.
source
Flora of North America @ eFloras.org
editor
Flora of North America Editorial Committee
project
eFloras.org
original
visit source
partner site
eFloras

Synonym

provided by eFloras
Bucholzia philoxeroides C. Martius, Nov. Actorum Acad. Caes. Leop.-Carol. Nat. Cur. 13(1): 107. 1825; Achyranthes philoxeroides (C. Martius) Standley; Telanthera philoxeroides (C. Martius) Moquin-Tandon.
license
cc-by-nc-sa-3.0
copyright
Missouri Botanical Garden, 4344 Shaw Boulevard, St. Louis, MO, 63110 USA
bibliographic citation
Flora of China Vol. 5: 427 in eFloras.org, Missouri Botanical Garden. Accessed Nov 12, 2008.
source
Flora of China @ eFloras.org
editor
Wu Zhengyi, Peter H. Raven & Hong Deyuan
project
eFloras.org
original
visit source
partner site
eFloras

Comprehensive Description

provided by North American Flora
Achyranthes philoxeroides (Mart.) Standley, Jour. Wash. Acad
Sci. 5: 74. 1915.
Bucholzia philoxeroides Mart. Nova Acta Acad. Iveop. -Carol. 13 1 : 315. 1826. Telanthera philoxeroides Moq. in DC. Prodr. 13 2 : 362. 1849. Telanthera philoxeroides obtusifolia Moq. in DC. Prodr. 13 2 : 363. 1849. Telanthera philoxeroides acutifolia Moq. in DC. Prodr. 13 2 : 363. 1849. Telanthera philoxeroides phyllantha Seub. in Mart. Fl. Bras. S 1 : 169. 1875. Telanthera philoxeroides denticulata Seub. in Mart. Fl. Bras. S 1 : 170. 1875. Alternanthera philoxeroides Griseb. Abh. Ges. Wiss. Gott. 24: 36. 1879.
Herbaceous perennial; stems stout, often fistulous, ascending or decumbent, 3-10 dm. long, simple or branched, villous in the axils of the leaves, elsewhere very sparsely villous or glabrous; leaves very short-petiolate, the blades elliptic-linear to elliptic or obovate, 3.5-11 cm. long, 0.5-2 cm. wide, acute or obtuse at the apex, acuminate or attenuate at the base, thick, glabrous; peduncles axillary or terminal, simple, 1-5 cm. long, pilose; spikes globose, 14-17 mm. thick, the flowers white; bracts one fourth as long as the sepals, broadly ovate, acute or acuminate, glabrous; sepals ovate-oblong, 6 mm. long, acute or acutish, subchartaceous, obscurely nerved, often serrulate near the apex; filaments linear-subulate, the staminodia exceeding the anthers, half as long as the sepals, ligulate, lacerate at the apex; style elongate, the stigma entire.
Type locality : Southern Brazil.
Distribution: In ponds and slow streams or in wet soil, adventive from North Carolina to Florida and Louisiana; also from Colombia to Brazil and Argentina,
license
cc-by-nc-sa-3.0
bibliographic citation
Paul Carpenter Standley. 1917. (CHENOPODIALES); AMARANTHACEAE. North American flora. vol 21(2). New York Botanical Garden, New York, NY
original
visit source
partner site
North American Flora

Alternanthera philoxeroides

provided by wikipedia EN

Alternanthera philoxeroides, commonly referred to as alligator weed, is a native species to the temperate regions of South America, which includes Argentina, Brazil, Paraguay and Uruguay.[2] Argentina alone hosts around 27 species that fall within the range of the genus Alternanthera.[2] Its geographic range once covered only the Parana River region of South America, but it has since expanded, having been introduced to over 30 countries, such as the United States, Japan, China, Australia, New Zealand and many more.[3] This invasive species is believed to have been accidentally introduced to these non-native regions through sediments trapped by, or attached to, tanks and cargo of ships travelling from South America to these various areas.

Description

Alternanthera philoxeroides can thrive in both dry and aquatic environments[4] and is characterized by whitish, papery flowers along its short stalks, irregular, or sprawling hollow stems, and simple and opposite leaf pattern sprouting from its nodes.[3] It is also considered a herbaceous plant due to its short-lived shoot system.[5] It produces horizontal stems, otherwise known as stolons, that can sprout up to 10 metres (33 ft) in length and thanks to its hollow stems, floats easily. This results in large clusters of stem amassing and create dense mats along the surface.[5] Bisexual flowers are small, white, and born on dense, axillary spikes (type of raceme).[6] Presence of a peduncle is a key trait that distinguishes this species from the sessile inflorescences of Alternanthera sessilis.[6] While seed production has been observed in its native range, there is currently no record of viable A. philoxeroides seeds in the introduced range. The weed's intricate root system can either allow them to hang free in the water to absorb nutrients or directly penetrate the soil/sediment and pull their nutrients from below.[5]

Invasive species - negative impacts

Alternanthera philoxeroides is considered a major threat to ecosystems because of the adverse effects it poses on both aquatic and terrestrial environments, as well as the negative influence it has on society.[4] The species features on the list of invasive alien species of Union Concern since 2017. This means that import and trade of this species is forbidden in the whole of the European Union.[7]

Impacts on vegetation

The presence of this invasive species disrupts the natural flow of water due to the dense mats created by its clusters of stems.[4] It out competes the native vegetation for space and solar energy through these dense mats because they form large clusters and limit the amount of light that submerged vegetation receives.[5] These compact clusters of stems also disturb the regular exchange of gases that occurs underneath the surface that directly influences aerobic processes, such as photosynthesis.[3] Aside from driving down the population of native aquatic vegetation, A. philoxeroides can also influence the growth and yield of crops in pastures and fields.[8] These dense mats can affect the natural flow of water that is used in irrigation systems and as well as affect the quality of the water by increasing the sedimentation present in the water.[4] Both of these factors must remain undisturbed for crops to grow well, and thus to provide a healthy yield for farmers, which will be discussed in the later section on its impacts on society. On top of this, the likelihood of flooding is higher due to the impaired drainage caused by the dense mats, which in turn can also damage crops.[4] This invasive species also has other negative impacts on the environment.[3]

Impacts on animals

As mentioned, the compact mats formed by this species can drive down the population of native vegetation in the environments it invades. This then becomes a major issue for native herbivores because their food source declines.[9] In addition, the dense mats present a challenge for the native wildlife by acting as a barrier between them and natural water sources.[9] However, even if they can reach the water, they are still at risk because the water quality can be contaminated by the increased sediments.[4] Thus, just as it did with the native vegetation, A. philoxeroides is also driving down the populations of the native wildlife as well.[10]

Impacts on society

Dense mats formed by this species influence the natural flow of water, which can impede various recreational activities, such as boating and fishing.[4] The disruption of flow can also have a negative impact on infrastructure when it comes to energy, such as the use of hydro-electric dams to power generators. The dense mats also present suitable ecological conditions that mosquitoes can thrive off of.[11] This is a commensal relationship between mosquitoes and A. philoxeroides because mosquitoes receive a breeding ground and the plant gains nothing nor loses anything. The increased population of mosquitoes can bring an increased risk of mosquito-borne diseases in humans.[11] Furthermore, the dense mats produced by A. philoxeroides may not present suitable ecological conditions for native species or humans to thrive off.

Reproduction and dispersal

This invasive plant depends solely on vegetative means to reproduce and disperse itself in the area it has invaded and established its roots. In its native geographic range, the species spreads to through means of producing viable seeds; however, it has been observed within its non-native ranges that it rarely produces viable seeds.[8] To accommodate this, the A. philoxeroides reproduces through fragmentation;[8] the plant can regenerate itself from small portions of stems or small leaf cuttings.[9] These small fragments of the plant can then be dispersed through human means and natural means; once it is dispersed, the fragments can then find suitable ecological conditions and root themselves and regenerate.[3]

Human dispersal

In effort to eradicate the species by manual means, such as mulching or pulling them out, if not removed efficiently, small stem fragments can be displaced to new areas.[4] Soil movement caused by earthmoving machinery is another example of how humans influence the dispersal of the plant.[8]

Natural dispersal

In aquatic environments, the A. philoxeroides can easily disperse its fragments by being sucked into the path of the waterways.[8] In terrestrial environments, the small fragments of stems and leaf cuttings can be dispersed through the natural movement of soil caused by erosion.[3] Thus, the geographic range of this invasive species can easily be expanded by any means necessary due to its ability to regenerate from practically nothing.

Methods of control

Preventive measures

Early detection is the best bet to ensure that the invasive species does not successfully colonize a non-native region because of its ability to regenerate and propagate from small portions of its stem or leaf cuttings. However, when that is not possible, the best that can be done is to limit and control the presence of A. philoxeroides in an area. Alternanthera philoxeroides can only establish itself in shallow waters no deeper than 2 metres (2 yards), so one method of control is to erect barriers in shallower areas to limit the amount of suitable space the plant has.[4] When it comes to terrestrial environments, overpopulating the area with native species can limit the suitable space available for it.[4] However, this method is only effective before the invasive plant has asserted itself in an area. Lastly, as previously mentioned, this plant is only able to produce viable seeds in its native geographic range and not in the areas it has invaded. Learning why that is - what ecological conditions make it produce only sterile seeds - could be key to developing further preventative measures against it.[2]

Biological measures

Insects have been released for the biological control of A. philoxeroides. The most successful and widely used is Agasicles hygrophila commonly called the alligator weed flea beetle; it has been released for biocontrol in Australia, China, Thailand, New Zealand, and the United States. However, their effectiveness is limited due to their inability to survive through temperatures lower than 11 °C (52 °F).[12] Amynothrips andersoni, the alligator weed thrips, and Vogtia malloi, the alligator weed stem borer, have also been released in the United States. These species result in immediate wilting and limit A. philoxeroides reproduction by colonizing its stems.[4] A variety of chemicals have been shown to be effective in controlling the plant, the most useful of which include glyphosate, triclopyr, fluridone, imazamox, and imazapyr; however, they must constantly be applied to be successful.[4]

Legality of sale and shipment in the United States

In 1956 A. philoxeroides was banned for sale or shipment in the United States, subject to a fine and/or imprisonment.[13] This law was repealed by HR133 [14][116th Congress (2019-2020)] on 12/27/2020.

See also

References

  1. ^ "Alternanthera philoxeroides". International Plant Names Index (IPNI). Royal Botanic Gardens, Kew; Harvard University Herbaria & Libraries; Australian National Botanic Gardens. Retrieved 2019-01-21.
  2. ^ a b c A.J. Sosa1; E. Greizerstein; M.V. Cardo; M.C. Telesnicki; M.H. Julien. "The evolutionary history of an invasive species: alligator weed, Alternanthera philoxeroides" (PDF). Bugwoodcloud.org. Retrieved 2022-03-30.
  3. ^ a b c d e f "NSW WeedWise". Weeds.dpi.nsw.gov.au. Retrieved 2021-11-23.
  4. ^ a b c d e f g h i j k l "Texas Invasives". Texasinvasives.org. Retrieved 2017-09-14.
  5. ^ a b c d "Alternanthera philoxeroides". Sms.si.edu. Retrieved 2017-09-14.
  6. ^ a b Godfrey, Robert K. (1981). Aquatic and wetland plants of southeastern United States : dicotyledons. Jean W. Wooten. Athens, Ga.: University of Georgia Press. ISBN 978-0-8203-4243-6. OCLC 756658568.
  7. ^ "European IAS Regulation". June 2021. Archived from the original on 2015-09-10.
  8. ^ a b c d e "Pest plant risk assessment : Alligator weed (Alternanthera philoxeroides)" (PDF). Daf.qld.gov.au. Retrieved 2022-03-30.
  9. ^ a b c "Details". Tsusinvasives.org. Retrieved 2017-09-14.
  10. ^ Roberts LIN; Sutherland ORW (1986). "A Review of Biological Control of Invertebrates Pests and Weeds in new Zealand 1874 to 1987". Alternanthera philoxeroides (C. Martius) Grisebach, Alligator weed (Amaranthaceae). UK: CAB. pp. 325–330. ISBN 0851986455. Retrieved 22 January 2019.
  11. ^ a b "Management and Control of Alligator Weed in Ponds and Lakes › Aquatic Biologists". Aquaticbiologists.com. Archived from the original on 2017-09-14. Retrieved 2017-09-14.
  12. ^ "Alligator weed (Alternanthera philoxeroides) - FactSheet". Nas.er.usgs.gov. Retrieved 2017-09-14.
  13. ^ "Transportation of water hyacinths". Bill No. 18 U.S. Code § 46 of 1 August 1956. United States Congress.
  14. ^ Cuellar, Henry (2020-12-27). "H.R.133 - 116th Congress (2019-2020): Consolidated Appropriations Act, 2041". Congress.gov. Retrieved 2020-12-29.

license
cc-by-sa-3.0
copyright
Wikipedia authors and editors
original
visit source
partner site
wikipedia EN

Alternanthera philoxeroides: Brief Summary

provided by wikipedia EN

Alternanthera philoxeroides, commonly referred to as alligator weed, is a native species to the temperate regions of South America, which includes Argentina, Brazil, Paraguay and Uruguay. Argentina alone hosts around 27 species that fall within the range of the genus Alternanthera. Its geographic range once covered only the Parana River region of South America, but it has since expanded, having been introduced to over 30 countries, such as the United States, Japan, China, Australia, New Zealand and many more. This invasive species is believed to have been accidentally introduced to these non-native regions through sediments trapped by, or attached to, tanks and cargo of ships travelling from South America to these various areas.

license
cc-by-sa-3.0
copyright
Wikipedia authors and editors
original
visit source
partner site
wikipedia EN