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Acer negundo
Acer negundo
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Acer negundo
Scientific classification Edit this classification
Kingdom: Plantae
Clade: Tracheophytes
Clade: Angiosperms
Clade: Eudicots
Clade: Rosids
Order: Sapindales
Family: Sapindaceae
Genus: Acer
Section: Acer sect. Negundo
Series: Acer ser. Negundo
Species:
A. negundo
Binomial name
Acer negundo
Native range of Acer negundo
Synonyms[2]
List
  • Acer californicum var. texanum Pax
  • Acer fauriei H.Lév. & Vaniot
  • Acer fraxinifolium Nutt.
  • Acer fraxinifolium Raf.
  • Acer lobatum Raf.
  • Acer nuttallii (Nieuwl.) Lyon
  • Acer trifoliatum Raf.
  • Acer violaceum (Booth ex G.Kirchn.) Simonk.
  • Negundo aceroides var. violaceum G. Kirchn.
  • Negundo aceroides subsp. violaceus (Booth ex G. Kirchn.) W.A. Weber
  • Negundo fraxinifolium var. crispum Loudon
  • Negundo fraxinifolium var. violaceum Booth ex Loudon
  • Negundo negundo (L.) H. Karst.
  • Negundo texanum (Pax) Rydb.
  • Rulac negundo (L.) Hitchc.
Female flowers
Male flowers

Acer negundo, also known as the box elder, boxelder maple, Manitoba maple or ash-leaved maple, is a species of maple native to North America from Canada to Honduras.[3] It is a fast-growing, short-lived tree with opposite, ash-like compound leaves. It is sometimes considered a weedy or invasive species, and has been naturalized throughout much of the world, including South America, Australia, New Zealand, South Africa, much of Europe, and parts of Asia.[4][5]

Description

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Acer negundo is a fast-growing and fairly short-lived tree that grows up to 10–25 metres (35–80 feet) tall, with a trunk diameter of 30–50 centimetres (12–20 inches), rarely up to 1 m (3 ft 3 in) diameter. It often has several trunks and can form impenetrable thickets.[5] The typical lifespan of box elder is 60 - 75 years. Under exceptionally favorable conditions, it may live to 100 years.[6]

The shoots are green, often with a whitish to pink or violet waxy coating when young. Branches are smooth, somewhat brittle, and tend to retain a fresh green color rather than forming a bark of dead, protective tissue. The bark on its trunks is pale gray or light brown, deeply cleft into broad ridges, and scaly.[7]

Unlike most other maples (which usually have simple, palmately lobed leaves), Acer negundo has pinnately compound leaves that usually have three to seven leaflets.[8] Simple leaves are also occasionally present; technically, these are single-leaflet compound leaves. Although some other maples (such as Acer griseum, Acer mandshuricum and the closely related A. cissifolium) have trifoliate leaves, only A. negundo regularly displays more than three leaflets. The leaflets are about 5–10 cm (2–4 in) long and 3–7 cm (1+142+34 in) wide with slightly serrate margins. Leaves have a translucent light green color and turn yellow in the fall.

The yellow-green flowers are small and appear in early spring, with staminate flowers in clusters on slender pedicels and pistillate flowers on drooping racemes 10–20 cm (4–8 in) long.

The fruit is a schizocarp of two single-seeded, winged samaras on drooping racemes. Each seed is slender, 1–2 cm (1234 in) long, with a 2–3 cm (341+14 in) incurved wing; they drop in autumn or they may persist through winter. Seeds are usually both prolific and fertile.[7]

Unlike most other maples, A. negundo is fully dioecious and both a male and female tree are needed for reproduction to occur.[9] The male and female flowers appear on separate plants,[10] with males featuring clusters that generally have four flowers together, while females appear as a raceme.[11]

Taxonomy

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The Box elder is not in the Elder genus Sambucus in the family Adoxaceae. A few botanists treat boxelder maple in its own distinct genus (Negundo aceroides) but this is not widely accepted.[citation needed]

Common names

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Indicative of its familiarity to many people over a large geographic range, A. negundo has numerous common names. The names "box elder" and "boxelder maple" are based upon the similarity of its whitish wood to that of boxwood and the similarity of its pinnately compound leaves to those of some species of elder.[12]

Other common names are based upon this maple's similarity to ash, its preferred environment, its sugary sap, a description of its leaves, its binomial name, and so on. These names include "Manitoba maple", "ash-leaf maple", "cut-leaved maple", "three-leaf maple", "ash maple", "sugar maple", "negundo maple", and "river maple".[13]

Names vary regionally. Box elder, boxelder maple, ash-leaved maple, and maple ash are among its common names in the United States. In Canada it is commonly known as Manitoba maple and occasionally as elf maple.[14] In the British Isles it is known as box elder[15] or ashleaf maple.[16] In Russia it is known as American maple (Russian: америка́нский клён, romanizedamerikansky klyon) as well as ash-leaf maple (Russian: клён ясенели́стный, romanizedklyon yasenelistny).

Because of its leaflets' superficial similarity to those of poison ivy, Acer negundo saplings are often mistaken for the allergenic plant. While both poison ivy and Acer negundo have compound leaves composed of three leaflets with ragged edges, Acer negundo exhibits an opposite branching pattern, as opposed to the alternating pattern of poison ivy.[17] Like poison ivy, Acer negundo is also a noted riparian species, and can often be found growing along riverbeds and in wet soils generally. For all these reasons, and despite their obvious differences, Acer negundo is sometimes referred to informally as the poison ivy tree.[18]

Subspecies

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Acer negundo is often divided into three or more subspecies, some of which were originally described as separate species. These are:[19]

  • Acer negundo subsp. negundo, native from the Atlantic Coast to the Rocky Mountains.[5]
  • Acer negundo subsp. interior (Britton) Sarg., with more leaf serration than the nominate subspecies and a more matte leaf surface, is native from Saskatchewan to New Mexico, between the eastern and western subspecies.[5]
  • Acer negundo var. arizonicum Sarg. is native to Arizona, New Mexico, and northern Mexico.[19]
  • Acer negundo subsp. californicum (Torr. & A.Gray) Sarg., with larger leaves with a velvety texture, is found in parts of California.[5][19]
  • Acer negundo subsp. mexicanum (DC.) Wesm. is native to Mexico, Guatemala, and Honduras.[19]
  • Acer negundo var. texanum Pax is native to the southern United States from Virginia to New Mexico, and to northeastern Mexico.[19]
  • Acer negundo var. violaceum (Booth ex Loudon) H.Jaeger is native to the Northeastern coastal United States and to the northern interior United States from the Ohio Valley to the Columbia River basin.[19]

Some authors further subdivide A. negundo subsp. negundo into a number of regional varieties but these intergrade and their maintenance as distinct taxa is disputed by many. Even the differences between recognized subspecies are probably a matter of gradient speciation.[citation needed]

Distribution and habitat

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Acer negundo often grows alongside waterbodies.
Growing as a weed in pavement crack in Russia

Acer negundo is native across much of the United States (mostly in the east)[8] and south-central Canada, and can be found as far south as Guatemala.

Box Elder County, Utah is named for this tree,[20] as is the town of Box Elder, South Dakota

Although native to North America, it is considered a weedy species in some areas, such as in parts of the Northeastern United States, and has increased greatly in these areas.[21] In 1928, Joseph Illick, chief forester for the state of Pennsylvania, wrote in Pennsylvania Trees[22] that box elder was "rare and localized" in the state. After World War II, box elder's rapid growth made it a popular landscaping tree in suburban housing developments despite its poor form, vulnerability to storm damage, and tendency to attract large numbers of box elder bugs. Intentional cultivation has thus made the tree far more abundant than it once was.[citation needed]

It can quickly colonize both cultivated and uncultivated areas and the range is therefore expanding both in North America and elsewhere. In Europe where it was introduced in 1688 as a park tree it is able to spread quickly and is considered an invasive species in parts of Central Europe, including Germany, the Czech Republic, Hungary, Slovenia, Poland and Russia where it can form mass growth in lowlands, disturbed areas, and riparian biomes on calcareous soils. It has also become naturalized in eastern China,[5] is listed as a pest invasive species in some of the cooler areas of the Australian continent,[4] and is invasive in the Rio de la Plata area.[23]

This species prefers bright sunlight. It often grows on flood plains and other disturbed areas with ample water supply, such as riparian habitats.[24] Human influence has greatly favored this species; it grows around houses and in hedges, as well as on disturbed ground and vacant lots.

Ecology

[edit]
Boxelder bugs (Boisea trivittata) feed on Acer negundo

Several birds and some squirrels feed on the seeds. The evening grosbeak uses them extensively.[25]

The boxelder bug (Boisea trivittata) lays its eggs on all maples, but prefers this species, clustering the eggs in bark crevices.[24] The rosy maple moth (Dryocampa rubicunda) also lays its eggs on the leaves of maple trees, including Acer negundo. The larvae feed on the leaves, and in very dense populations can cause defoliation.[26]

Small galls are formed on the leaves by a bladder mite, Aceria negundi. A gall midge, Contarinia negundinis joins and enlarges the galls of Aceria negundi. The midge sometimes creates a separate, tubular gall on the midrib or veins of the undersides of the leaves.[24]

The cottony maple leaf scale, Pulvinaria acericola, occurs on the foliage of Acer negundo.[24] A leaf spot fungus, Septoria negundinis creates black-ringed lesions on the leaves.[24]

Cultivation

[edit]
'Variegatum' cultivar with white-margined leaves

Although its weak wood, irregular form, and prolific seeding might make it seem like a poor choice for a landscape tree, A. negundo is one of the most common maples in cultivation. Long-term success has been noted as far north as Yellowknife.[27] Many cultivars have been developed, such as:[5]

  • 'Auratum' – yellowish leaves with smooth undersides
  • 'Aureomarginatum' – creamy yellow leaf margins
  • 'Baron' – Hardier & seedless variety
  • 'Elegans' – distinctively convex leaves
  • 'Flamingo' – pink and white variegation (very popular)
  • 'Pendulum' – with weeping branches.
  • 'Variegatum' – creamy white leaf margins
  • 'Violaceum' – younger shoots and branches have bluish color

Toxicity

[edit]

A protoxin present in the seeds of Acer negundo, hypoglycin A, has been identified as a major risk factor for, and possibly the cause of, a disease in horses, seasonal pasture myopathy (SPM). SPM is an equine neurological disease which occurs seasonally in certain areas of North America and Europe, with symptoms including stiffness, difficulty walking or standing, dark urine and eventually breathing rapidly and becoming recumbent. Ingestion of sufficient quantities of box elder seeds or other parts of the plant results in breakdown of respiratory, postural, and cardiac muscles. The cause of SPM was unknown for centuries despite the disease being well known among affected areas and was only positively determined in the 21st century.[28][29][30] It is analogous to Jamaican vomiting sickness in humans, also caused by hypoglycin A.

Acer negundo pollen, which is released in winter or spring (varying with latitude and elevation)[31] is a severe allergen.[31]

Uses

[edit]

Wood

[edit]
Heartwood of Acer negundo with red stain

Although its light, close-grained, soft wood is considered undesirable for most commercial uses, this tree has been considered as a source of wood fiber, for use in fiberboard.[32] There is also some commercial use of the tree for various decorative applications, such as turned items (bowls, stem-ware, pens). Such purposes generally use burl or injured wood, as the injured wood develops a red stain.[33]

The wood has been used for a variety of purposes by Native Americans, such as by the Navajo to make tubes for bellows,[34] by the Cheyenne to make bowls,[35] and by the native peoples of Montana who use the large trunk burls or knots to make bowls, dishes, drums, and pipe stems.[36] The Tewa use the twigs as pipe stems[37] and the Keres make the twigs into prayer sticks.[38]

The Dakota people and the Omaha people[39][40] make the wood into charcoal, which is used in ceremonial painting and tattooing.[41][39] The Kiowa burn the wood in the altar fire during the peyote ceremony.[42]

Acer negundo was identified as the material used in the oldest extant wood flutes from the Americas. The flutes, excavated by Earl H. Morris in 1931 in Northeastern Arizona, have been dated to 620–670 CE.[43]

Medicinal use

[edit]

Acer negundo has been used by Native Americans for several medicinal purposes. The Cheyenne burn the wood as incense for making spiritual medicines,[36] and during Sun Dance ceremonies.[36] The Meskwaki use a decoction of the inner bark as an emetic,[44] and the Ojibwa use an infusion of the inner bark for the same purpose.[45]

As food

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The sap has been used to make syrup by Native Americans, including the Dakota,[41] Omaha,[46][39] Pawnee, Ponca, Winnebago,[39] Cree,[47] Sioux,[48] and the indigenous people of Montana.[36] The Chiricahua and Mescalero Apache dry scrapings of the inner bark and keep it as winter food, and they also boil the inner bark until sugar crystallizes out of it.[49] The Cheyenne mix the boiled sap with shavings from the inner sides of animal hides and eat them as candy.[36][50] The Ojibwa mix the sap with that of the sugar maple and drink it as a beverage.[51]

Citations

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  1. ^ Barstow, M.; Crowley, D.; Rivers, M.C. (2017). "Acer negundo". IUCN Red List of Threatened Species. 2017 e.T62940A3117065. doi:10.2305/IUCN.UK.2017-3.RLTS.T62940A3117065.en. Retrieved 13 November 2021.
  2. ^ World Flora Online Plant List
  3. ^ "Acer negundo L." Plants of the World Online. Royal Botanic Gardens, Kew. Retrieved 2024-12-08.
  4. ^ a b "Acer negundo". keyserver.lucidcentral.org. Weeds of Australia. Retrieved 4 December 2018.
  5. ^ a b c d e f g van Gelderen, C.J. & van Gelderen, D.M. (1999). Maples for Gardens: A Color Encyclopedia.
  6. ^ CABI datasheet. Available at https://www.cabi.org/isc/datasheet/2862 (accessed 04/10/2022)
  7. ^ a b Keeler, H. L. (1900). Our Native Trees and How to Identify Them. New York: Charles Scribner's Sons. pp. 85–87.
  8. ^ a b Arno, Stephen F.; Hammerly, Ramona P. (2020) [1977]. Northwest Trees: Identifying & Understanding the Region's Native Trees (field guide ed.). Seattle: Mountaineers Books. pp. 261–262. ISBN 978-1-68051-329-5. OCLC 1141235469.
  9. ^ Maeglin & Ohmann (1973), p. 359
  10. ^ "Acer negundo". Royal Horticultural Society. Retrieved 14 October 2024. male and female flowers on separate plants
  11. ^ "Acer negundo". Van den Berk Nurseries. Retrieved 14 October 2024. compact clusters of usually four flowers together. The female flowers appear in long pendent raceme
  12. ^ "DePauw Nature Park Field Guide to Trees" (PDF). DePauw University. p. 14. Retrieved 2018-05-24.
  13. ^ "Windsor Plywood". Some of the common names given in this reference are questionable, "stinking ash" and "black ash" typically refer to Ptelea trifoliata and Fraxinus nigra, respectively. This reference is retained as an example of the confusion which arises when plants such as A. negundo are discussed by other than their scientific names.
  14. ^ "Community trees of the Prairie provinces". Natural Resources Canada. 2007-02-22. Archived from the original on 2008-05-18.
  15. ^ "Acer negundo". www.rhs.org. Royal Horticultural Society. Retrieved 26 September 2019.
  16. ^ BSBI List 2007 (xls). Botanical Society of Britain and Ireland. Archived from the original (xls) on 2015-06-26. Retrieved 2014-10-17.
  17. ^ Trees with Don Leopold - boxelder, 21 October 2011, archived from the original on 2021-12-12, retrieved 2021-06-19
  18. ^ Tree Talk: Boxelder, 8 May 2019, archived from the original on 2021-12-12, retrieved 2021-06-19
  19. ^ a b c d e f Acer negundo L. Plants of the World Online, Kew Science. Accessed 26 January 2023
  20. ^ "Utah History Encyclopedia". www.uen.org. Retrieved 2025-01-15.
  21. ^ Uva, R.H., J.C. Neal, and J.M. DiTomaso. 1997. Weeds of the Northeast. Cornell University Press. Ithaca, New York.
  22. ^ Illick, Joseph S. (1928). Pennsylvania Trees (4th ed.). [Harrisburg., Pa.]: Pennsylvania Department of Forests and Waters. p. 203.
  23. ^ Passarelli, L. M.; Rolleri, C. H.; Ciciarelli, M. d. l. M.; Dedomenici, A. C.; González, G. (2014). "Flora vascular de humedales permanentes y transitorios bonaerenses (Buenos Aires, Argentina)". Botánica Complutensis. 38: 143. doi:10.5209/rev-BOCM.2014.v38.45782 (inactive 23 October 2025). Retrieved 6 December 2024.{{cite journal}}: CS1 maint: DOI inactive as of October 2025 (link)
  24. ^ a b c d e Wilhelm, Gerould; Rericha, Laura (2017). Flora of the Chicago Region: A Floristic and Ecological Synthesis. Indiana Academy of Sciences.
  25. ^ DeGraaf, Richard M. (2002). Trees, Shrubs, and Vines for Attracting Birds. UPNE. ISBN 978-1-58465-215-1.
  26. ^ "Dryocampa rubicunda (rosy maple moth)". Animal Diversity Web. Retrieved 2017-11-14.
  27. ^ "Manitoba Maple (Acer negundo)". 31 August 2018.
  28. ^ "Seasonal pasture myopathy". Michigan State University. Archived from the original on 3 January 2018. Retrieved 3 January 2018.
  29. ^ Anna Renier. "Seasonal pasture myopathy cause identified". University of Minnesota Extension. Archived from the original on 2017-11-27. Retrieved 2018-01-03.
  30. ^ Valberg, S.J.; Sponseller, B.T.; Hegeman, A.D.; Earing, J.; Bender, J.B.; Martinson, K.L.; Patterson, S.E.; Sweetman, L. (July 2013). "Seasonal pasture myopathy/atypical myopathy in North America associated with ingestion of hypoglycin A within seeds of the box elder tree". Equine Veterinary Journal. 45 (4): 419–426. doi:10.1111/j.2042-3306.2012.00684.x. ISSN 2042-3306. PMID 23167695. S2CID 206002430.
  31. ^ a b "Box Elder, Ash-Leaf Maple (Acer negundo)". PollenLibrary.com.
  32. ^ Maeglin & Ohmann (1973), pp. 360-361
  33. ^ Maeglin & Ohmann (1973), p. 360
  34. ^ Elmore, Francis H. (1944). Ethnobotany of the Navajo. Santa Fe, NM. School of American Research (p. 62)
  35. ^ Hart, Jeffrey A. (1981). "The Ethnobotany of the Northern Cheyenne Indians of Montana." Journal of Ethnopharmacology 4:1–55 (p. 46).
  36. ^ a b c d e Hart, Jeff (1992). Montana Native Plants and Early Peoples. Helena. Montana Historical Society Press (p. 4)
  37. ^ Robbins, W.W., J.P. Harrington and B. Freire-Marreco (1916). "Ethnobotany of the Tewa Indians." SI-BAE Bulletin #55 (p. 38).
  38. ^ Swank, George R. (1932). The Ethnobotany of the Acoma and Laguna Indians. University of New Mexico, M.A. Thesis (p. 24).
  39. ^ a b c d Gilmore, Melvin R. (1919). "Uses of Plants by the Indians of the Missouri River Region." SI-BAE Annual Report #33 (p. 101)
  40. ^ Gilmore, Melvin R. (1913). "A Study in the Ethnobotany of the Omaha Indians." Nebraska State Historical Society Collections 17:314–57. (p. 336).
  41. ^ a b Gilmore, Melvin R. (1913). "Some Native Nebraska Plants With Their Uses by the Dakota." Nebraska State Historical Society Collections 17:358–70 (p. 366)
  42. ^ Vestal, Paul A. and Richard Evans Schultes (1939). The Economic Botany of the Kiowa Indians. Cambridge MA. Botanical Museum of Harvard University (p. 40)
  43. ^ Clint Goss (2011). "Anasazi Flutes from the Broken Flute Cave". Retrieved 2011-10-18.
  44. ^ Smith, Huron H. (1928). "Ethnobotany of the Meskwaki Indians." Bulletin of the Public Museum of the City of Milwaukee 4:175–326 (p. 200)'
  45. ^ Smith, Huron H. (1932). "Ethnobotany of the Ojibwe Indians." Bulletin of the Public Museum of Milwaukee 4:327–525 (p. 353)
  46. ^ Gilmore, Melvin R. (1913). "A Study in the Ethnobotany of the Omaha Indians." Nebraska State Historical Society Collections 17:314–57. (p. 329).
  47. ^ Johnston, Alex (1987). Plants and the Blackfoot. Lethbridge, Alberta. Lethbridge Historical Society (p. 44).
  48. ^ Blankinship, J. W. (1905). "Native Economic Plants of Montana." Bozeman. Montana Agricultural College Experimental Station, Bulletin 56 (p. 16)
  49. ^ Castetter, Edward F. and M. E. Opler (1936). "Ethnobiological Studies in the American Southwest III. The Ethnobiology of the Chiricahua and Mescalero Apache." University of New Mexico Bulletin 4(5):1–63 (p. 44).
  50. ^ Hart, Jeffrey A. (1981). "The Ethnobotany of the Northern Cheyenne Indians of Montana." Journal of Ethnopharmacology 4:1–55 (p. 13).
  51. ^ Smith, Huron H. (1932). "Ethnobotany of the Ojibwe Indians." Bulletin of the Public Museum of Milwaukee 4:327–525 (p. 394).

General and cited references

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[edit]
Revisions and contributorsEdit on WikipediaRead on Wikipedia
from Grokipedia
Acer negundo, commonly known as boxelder, ash-leaved , or Manitoba maple, is a fast-growing tree in the family native to . It typically reaches heights of 10–20 m (30–65 ft) with a broad, rounded crown and opposite, pinnately compound leaves consisting of 3–5 coarsely toothed, often lobed leaflets that are 5–10 cm long and resemble those of trees. The tree is usually dioecious, producing small, yellow-green flowers in early spring—males in clusters and females in drooping racemes—followed by paired, winged samaras 2.5–4 cm long that mature in summer and aid in wind dispersal. As the most widely distributed maple species in North America, A. negundo ranges from southern and the westward to the , southward through central to , and is naturalized in parts of and . It thrives in riparian and habitats with moist to wet soils, such as riverbanks and low woods, but tolerates a wide variety of conditions including , urban pollution, clay, and alkaline soils once established, though it prefers neutral to slightly alkaline, well-drained loams. Ecologically, it functions as an early-successional , contributing to , streambank stabilization, and provision for , including seeds for birds and small mammals, browse for deer, and cover for livestock in arid regions. A. negundo has several practical uses, including as a hardy shade or shelterbelt in cold or dry climates due to its rapid growth rate of up to 2.5 cm (1 in) per year in diameter for the first 15–20 years, though it is short-lived (typically 60–100 years) and prone to weak wood, diseases like anthracnose, and pests such as borers. The light-colored wood is utilized for pulp, crates, boxes, low-grade furniture, and , while the sap can be tapped for , and Native American communities historically used it for , , and dyes. However, its suckering habit and potential invasiveness in non-native areas limit its recommendation for some landscapes.

Taxonomy and Classification

Common Names

Acer negundo is commonly known as box elder, boxelder , Manitoba maple, and ash-leaved maple. The name "box elder" originates from the tree's visual resemblance to elder ( species) and its fine-grained wood, which is similar to that of boxwood () or historically used for crafting boxes and crates. "Ash-leaved maple" reflects the pinnately compound leaves that mimic those of ash trees ( species), a adopted by early European settlers upon observing the plant in . In regional contexts, particularly in the Canadian prairies, it is referred to as , emphasizing its prevalence in that area. The subspecies A. negundo subsp. californicum is specifically called California box elder, highlighting its adaptation to western environments. Additionally, it is known as in some locales, alluding to the typical trifoliate structure of its leaves.

Subspecies and Varieties

Acer negundo was first described by in his 1753 publication , where it was placed in the genus Acer within the family Aceraceae (now ). Taxonomic revisions in the 20th century, particularly by van Gelderen et al. in 1994, recognized intraspecific variation through the delineation of subspecies based on differences in leaflet morphology, pubescence on branchlets and leaves, and samara wing angles. Four main subspecies are recognized by van Gelderen et al. (1994), each associated with distinct geographic regions and morphological traits, though some taxonomists treat certain taxa as varieties and note intergradation, leading to ongoing debate in classification. , the nominate subspecies, occurs in eastern and is characterized by typically 3–5 glabrous leaflets per and samaras with divergent wings forming an acute angle. (also known as subsp. interius) is found in the central plains of , distinguished by increased , a more matte surface, and often 3–7 leaflets with variable pubescence; it is sometimes treated as synonymous with var. texanum. is native to and adjacent areas, featuring pubescent branchlets, 3–7 ovate leaflets that are tomentose when young, and pubescent samaras with wings at a wide angle. ranges from to , with 3–5 ovate leaflets that are dark green above and tomentose beneath, along with glabrous branchlets and samaras having nearly parallel wings. Within these subspecies, certain varieties represent regional forms, particularly under subsp. californicum. Var. arizonicum is a southwestern variant with consistently 3 leaflets, pale green foliage, and glabrous samaras, occurring in , , and . Var. texanum, found in the and , has 3–5 dull green leaflets that are coarsely serrate in the upper half and samaras with moderately divergent wings. These subdivisions highlight the species' adaptability.

Description and Morphology

Physical Characteristics

_Acer negundo is a medium-sized that typically reaches heights of 10 to 25 meters and spreads 10 to 20 meters wide, forming a broad, rounded to irregular crown. It exhibits rapid growth, particularly in the first 15 to 20 years, with annual diameter increases up to 2.5 cm, but it is short-lived, averaging 60 years and rarely exceeding 75 to 100 years. The often develops a short, tapering bole and bushy , with branching that contributes to its distinctive structure. The leaves are and pinnately , usually consisting of 3 to 5 (occasionally up to 7) coarsely toothed or serrated leaflets that are ovate to lanceolate, measuring 5 to 10 cm long and 3 to 6 cm wide, with the entire leaf blade reaching 13 to 20 cm in length. They are bright green above and paler beneath during the , turning to a dull yellow in fall. The bark is light gray to brown, initially smooth and thin, becoming furrowed with shallow, interlacing ridges or deeper fissures on mature trees. Twigs are stout, green to purplish, often with a waxy coating, and bear V-shaped leaf scars. exhibit variations in leaf shape and characteristics. Acer negundo is dioecious, producing small, yellowish-green flowers about 5 mm long in early spring from to May, before or with the leaves; male flowers occur in fascicles, while female flowers form drooping racemes. The fruits are paired, V-shaped winged samaras, 2.5 to 4 cm long, that mature from August to October, turning light tan and persisting into winter. The is shallow and fibrous, often extensive with surface , and prone to suckering from the root collar or stumps.

Reproduction and Growth

Acer negundo is dioecious, with separate male (staminate) and female (pistillate) trees producing imperfect flowers that are wind-pollinated. Flowering occurs in spring from March to May, typically before or simultaneously with leaf emergence, in fascicles for males and drooping racemes for females. The small, yellow-green flowers measure about 5 mm long and are visited occasionally by bees, though wind remains the primary pollination vector. Seed production begins at 8 to 11 years of age, with individual trees producing abundant crops annually thereafter. Female trees develop paired samaras—winged nutlets 2.5 to 4 cm long—that ripen from to and are dispersed primarily by , though aids in riparian habitats. These samaras remain viable primarily in the first year after dispersal, with requiring 60 to 90 days of stratification at around 1°C, after which viability declines rapidly in subsequent years. As a , Acer negundo exhibits rapid juvenile growth, often reaching 0.6 to 0.8 m in height annually during the first 15 to 20 years, though this rate slows with maturity. increases by up to 2.5 cm per year initially, contributing to its quick establishment in disturbed sites. Regeneration occurs both sexually via seeds and asexually through root sprouts or suckers from stumps, particularly in younger trees, enabling clonal spread. The life cycle of Acer negundo is relatively short, with an average lifespan of 60 years and a maximum of about 100 years under optimal conditions. Peak seed production aligns with early maturity at 10 to 20 years, after which growth and reproductive output gradually decline, reflecting its adaptation as a short-lived opportunist in dynamic environments. Phenologically, leaf-out occurs in early spring alongside flowering, with foliage persisting through summer. In autumn, typically by October, leaves turn a dull yellow before dropping gradually through fall and into winter, marking the transition to dormancy.

Distribution and Habitat

Native Range

Acer negundo, commonly known as boxelder, is native to a broad expanse across North America, extending from southern Canada, including regions from Alberta to Nova Scotia, southward to Guatemala in Central America, and westward to California and the Rocky Mountains. This wide distribution makes it one of the most extensively ranging maple species on the continent. Within its native range, A. negundo predominantly inhabits riparian zones, floodplains, and moist bottomlands along streams and rivers. It thrives in environments with periodic flooding and tolerates wet soils, while also accommodating full sun to partial shade conditions. The species shows adaptability to various soil types, including clay, loam, and sand, though it prefers moist, well-drained substrates. In terms of climate, it is suited to USDA hardiness zones 2 through 9, with optimal performance in zones 2 to 10. Historically, the pre-colonial distribution of A. negundo was closely associated with riverine systems and alluvial soils, reflecting its ecological affinity for dynamic, water-influenced habitats, and no major range contractions have been documented in modern assessments. Certain subspecies exhibit regional specificity within this range, such as var. californicum in western states.

Introduced Range and Invasiveness

Acer negundo, native to , has been introduced to numerous regions worldwide, primarily for ornamental and amenity purposes since the late 17th century. It was first planted in the in 1688 and subsequently spread across , where it is now naturalized in countries including , , , , and . In , introductions occurred in West () and eastern , with naturalization documented since the late . The species has also been established in , , (e.g., and ), and , often through deliberate planting along waterways and in urban areas, leading to widespread regeneration outside cultivation. In many introduced areas, particularly in and , Acer negundo is regarded as invasive due to its rapid colonization of disturbed habitats, especially riparian zones. It spreads aggressively via abundant wind-dispersed seeds and through root suckers and broken branches, forming dense monospecific stands that outcompete native vegetation in resource-rich environments. In , its range has expanded northward since the 2000s, from to the , facilitated by human-mediated dispersal and potentially warmer conditions in some areas, as evidenced by niche shift studies. In and , its spread remains more recent and localized but is increasingly noted along watercourses. The invasiveness of Acer negundo leads to significant ecological impacts, primarily in and riverine ecosystems where it displaces native riparian like and through superior growth rates and under high light and nutrient availability. This competition reduces understory , alters microbial communities via leaf litter , and may destabilize riverbanks by changing hydrological patterns and increasing risk in invaded areas. In urban riparian forests of , high canopy cover from A. negundo has been linked to decreased plant and limited recreational use due to dense thickets. While overall impacts are moderate compared to other invasives, its pioneer nature exacerbates habitat degradation in disturbed sites. Management of Acer negundo focuses on prevention and localized control in sensitive habitats, with mechanical methods like —removing a ring of bark to disrupt nutrient flow—proving effective and eco-friendly for mature trees, achieving high mortality rates without chemicals. Cutting followed by immediate application of herbicides such as or to stumps prevents resprouting and is recommended for seedlings and saplings in riparian areas, though repeated treatments are often necessary due to prolific regeneration. In , integrated approaches combining cut-stump treatments with monitoring along waterways are promoted to curb spread, emphasizing early detection to avoid establishment. Biological controls remain limited, and ongoing research highlights the need for adaptive strategies amid potential climate-driven expansions.

Ecology and Interactions

Wildlife Interactions

Acer negundo primarily relies on wind for pollination, with its inconspicuous flowers producing abundant pollen that is dispersed anemophilously across native North American habitats. However, the tree's early spring blooms occasionally attract native bees and other insects, which visit for nectar and pollen, contributing to pollinator foraging in riparian and floodplain ecosystems. The 's winged samaras serve as a key resource for various wildlife, including birds such as evening grosbeaks and finches, which consume and aid in dispersal through caching and flight. Squirrels and , like chipmunks, also eat and scatter , enhancing their spread beyond wind dispersal while providing nutritional sustenance during winter months when other resources are scarce. These interactions underscore the samaras' value as a persistent, energy-rich source for consumers in native food webs. Browsing by white-tailed and occurs on twigs and foliage, particularly in fall, positioning A. negundo as a secondary species in riparian zones. Rabbits similarly feed on young shoots and leaves, though mature trees develop some resistance; this herbivory supports local by integrating the tree into floodplain dynamics where it stabilizes soils and fosters habitat diversity. A. negundo forms symbiotic associations with arbuscular mycorrhizal fungi, which enhance nutrient uptake, particularly and , in nutrient-poor soils. Globally assessed as secure (equivalent to Least Concern), A. negundo plays a vital role in supporting declining riparian by providing and in increasingly fragmented ecosystems.

Pests, Diseases, and Environmental Impacts

Acer negundo is susceptible to several insect pests that can affect its foliage, seeds, and overall vigor. The boxelder bug (Boisea trivittata) is a common nuisance pest that feeds on sap from developing seeds, leaves, and fruits, potentially causing discoloration and minor defoliation, though it rarely causes serious damage to the tree itself. , particularly the boxelder aphid (Periphyllus negundinis), colonize leaves and shoots, sucking sap and producing honeydew that promotes ; heavy infestations can stunt growth in young trees. Borers such as the maple callus borer (Synanthedon acerni) and polyphagous shot hole borer (Euwallacea fornicatus) tunnel into the bark and wood, weakening branches and facilitating secondary infections, especially in stressed trees. Larvae of the (Dryocampa rubicunda), known as greenstriped maple worms, can defoliate leaves during outbreaks, though this is typically not lethal to mature individuals. Fungal and bacterial diseases also pose significant threats to A. negundo. Verticillium wilt, caused by Verticillium dahliae and V. albo-atrum, leads to vascular discoloration, wilting, and branch dieback by blocking water flow in the xylem; it affects over 300 plant species and is particularly problematic in cool, moist soils. Leaf spot diseases, including those from Cercospora spp., Phyllosticta minima, and Septoria aceris, produce necrotic spots that can lead to premature defoliation, especially in wet conditions. Cankers, such as those caused by Inonotus rickii or Fusarium spp., result in sunken lesions, bark cracking, and dieback, often entering through wounds and contributing to rot in the trunk or branches. Additionally, eriophyid mites like Aceria negundi induce galls, including bladder galls and erineum patches on leaves, which distort growth but seldom cause economic loss. Environmental stressors exacerbate A. negundo's vulnerabilities due to its weak structure. The species shows moderate in native riparian habitats but becomes intolerant in drier, upland sites, leading to leaf scorch and reduced growth during prolonged dry periods. Ice storms and heavy accumulation frequently cause breakage, as the soft, brittle fails under load, contributing to long-term canopy decline. , including warmer winters, is expanding the ranges of pests like the polyphagous shot hole borer, increasing infestation risks in northern latitudes. Introduced populations of A. negundo often exhibit low compared to native ones, stemming from founder effects during invasions, which heightens vulnerability to pests and diseases; for instance, European populations show reduced allelic richness, limiting adaptive responses to novel stressors. Recent genomic analyses, including those from 2022-2023, highlight expanded families in A. negundo related to stress tolerance, such as RNA modification and response, aiding its invasiveness but underscoring the need to preserve native for resilience. Management of pests and diseases in A. negundo employs (IPM) strategies tailored to context. In native ranges, cultural practices like proper watering to mitigate drought stress, combined with targeted insecticides for severe or borer outbreaks, help maintain health without broad-spectrum applications. In invasive contexts, such as , control focuses on mechanical removal or to limit spread, with minimal chemical intervention to avoid non-target effects, while monitoring genetic bottlenecks informs restoration efforts in native areas.

Cultivation

Growing Conditions

Acer negundo, commonly known as boxelder, prefers full sun for optimal growth but tolerates partial shade effectively. It thrives in moist to wet soil conditions and demonstrates high flood tolerance, capable of withstanding prolonged inundation in riparian zones. Once established, it also exhibits reasonable , making it suitable for variable moisture regimes. This species adapts well to a wide range of types, including poor, compacted, and saline conditions, with a tolerance spanning 5.0 to 7.5. Its enables it to stabilize disturbed or low-quality sites effectively. It performs in sandy loams to heavy clays, further enhancing its versatility in challenging environments. Acer negundo is hardy in USDA zones 2 to 9 and establishes rapidly in both urban and rural settings, often reaching maturity within a few years due to its fast growth rate. However, its brittle wood structure renders branches susceptible to breakage during storms, and its typical lifespan of about 60 years (rarely exceeding 100 years) restricts its suitability for long-term landscape planning. Forestry reports emphasize A. negundo's value for along waterways, leveraging its quick and extensive to prevent loss in riparian areas.

Cultivars and Propagation

Acer negundo has several notable selected primarily for ornamental foliage traits that enhance its appeal in . The 'Flamingo' features variegated leaves with pink and white margins, most prominent on new growth in spring, and is a clone that produces no seeds, making it suitable for urban settings to minimize . 'Variegatum', a clone, displays broad white margins on its compound leaves, though it produces winged fruits that can contribute to messiness. 'Aureomarginatum' offers creamy-yellow edges on the leaflets, providing bright contrast, but it is prone to reversion to green foliage. Other representative selections include 'Aureovariegatum' with yellow-spotted and margined leaves and 'Sensation' with reddish-tinged emerging foliage that turns vibrant in fall. Cultivars are chosen based on traits that address needs, such as variegated or colored foliage for visual interest in parks and gardens, seedless male forms to reduce maintenance, and hardy growth for tolerant urban or plantings. Dwarf or compact varieties, like certain selections with narrower crowns, suit space-limited environments, while overall adaptability to poor soils supports their use in reclamation projects. Propagation of Acer negundo is straightforward and relies on multiple methods to accommodate both wild and cultivated forms. Seeds, collected in fall from female trees, require to break the hard coat—via mechanical nicking or hot water soak—followed by three months of cold moist stratification at 1–5°C to overcome and achieve rates of 5–20% in spring. or semi-ripe cuttings taken from new growth in through summer readily under , with success enhanced by indolebutyric acid application, yielding vigorous in 4–6 weeks. cuttings from dormant branches in winter also propagate well, particularly with treatment, producing shoots with greater diameter and compared to softer material. Vegetative spread occurs naturally via suckers and stump sprouts, which can be dug and transplanted in early spring for clonal . is uncommon due to poor compatibility with rootstocks, limiting its use to specialized breeding. Breeding efforts for Acer negundo cultivars began in the in and , focusing on s and mutations for ornamental ; for instance, 'Aureomarginatum' was introduced before 1885 by Zöschen nursery in , and 'Auratum' originated as a in 1891 at Späth's nurseries in . Mid-20th-century developments included radiation-induced mutants, with about 15 described by 1965, though many are no longer in cultivation. Later selections, such as 'Flamingo' raised in 1976 in the , emphasized stable and sterility. These cultivars are widely available in nurseries across and for uses like windbreaks and screens, valued for their rapid establishment, but planting is discouraged in regions prone to invasiveness, such as parts of the and , where they can outcompete natives and spread via seeds or suckers.

Toxicity and Safety

Toxicity to Animals

Acer negundo, commonly known as boxelder, contains the toxin hypoglycin A (HGA) primarily in its seeds and young sprouts, which can cause severe muscle damage and myopathy in animals upon ingestion. This non-proteinogenic amino acid is metabolized into methylenecyclopropylacetyl-CoA (MCPA-CoA), a metabolite that inhibits medium- and short-chain acyl-CoA dehydrogenases, disrupting beta-oxidation of fatty acids and leading to an acquired multiple acyl-CoA dehydrogenase deficiency (MADD)-like syndrome. Recent research up to 2023 has further elucidated these pathways, including the detection of HGA metabolites in animal tissues and fluids, confirming the toxin's rapid absorption and bioactivation in the liver and muscles. As of 2025, ongoing research continues to monitor HGA-related risks in introduced ranges. In horses, ingestion of boxelder seeds is strongly associated with seasonal pasture myopathy (SPM), a potentially fatal condition most common in during fall and winter when fallen seeds accumulate on pastures amid sparse . Symptoms typically include profound weakness, recumbency, muscle tremors, excessive sweating, rapid breathing, and dark urine due to , with mortality rates exceeding 90% in affected cases; even small quantities, such as 500-1000 seeds, can deliver a toxic dose depending on the horse's size and seed HGA concentration. Documented outbreaks have occurred across the and , often in overgrazed or drought-stressed pastures near boxelder trees. While are the most susceptible species, HGA from Acer species may pose a potential to and other ruminants, though natural incidents are rare or undocumented due to differences in behavior and metabolism. Wildlife, such as and goats, has shown vulnerability in controlled settings, with fatal following consumption of boxelder foliage or seeds. Birds and small mammals frequently consume boxelder seeds without apparent adverse effects, indicating low in these despite high exposure; serve as a winter food source for finches, grosbeaks, and squirrels, with no reported intoxication cases in avian populations. Management strategies to mitigate risks include off boxelder trees in pastures, removing accumulated seeds during fall and winter, and monitoring for early symptoms in at-risk animals, particularly in regions like the Midwest and where the tree is prevalent. In , similar myopathies linked to HGA from introduced Acer negundo have been noted, though less commonly than from native like sycamore maple.

Human Health Concerns

Acer negundo, commonly known as boxelder, poses several health concerns to humans, primarily through its , sap, and potential for . The tree's is highly allergenic, with reported rates reaching 32.8% among patients tested in New York between 1993 and 2000, and it is a significant trigger for respiratory allergies. Exposure often leads to hay fever symptoms such as sneezing, runny nose, itchy eyes, and congestion, as well as exacerbations and rhino-conjunctivitis, particularly during peak release periods from late April to early May when flowering occurs. High pollen concentrations have been associated with a 2.1% increase in -related admissions in affected regions. Contact with the tree's pollen or wood dust can cause skin irritation, including characterized by red rashes and blisters in sensitive individuals, though such reactions are rare and documented in only a few case studies. Ingesting parts of the plant, such as seeds, is not known to cause in humans, though general caution is advised for unknown effects. Occupational exposure heightens risks for landscapers and urban workers handling A. negundo, as prolonged contact with during trimming or planting can intensify allergic responses, including worsened and symptoms. Urban planning considerations recommend limiting A. negundo plantings in high-density areas to reduce community pollen loads, as supported by 2024 analyses of tree species' allergenic impacts in cities like New York. Mitigation strategies include avoiding high-pollen areas during spring peaks, using air purifiers indoors, and employing antihistamines or nasal corticosteroids for symptom relief; may be considered for severe cases. Recent studies continue to explore allergenicity enhancements due to and interactions, emphasizing the need for low-allergen alternatives in landscaping.

Uses

Wood and Material Applications

The wood of Acer negundo, commonly known as boxelder, is characterized by its softness, lightness, and straight grain, making it suitable for non-structural applications but limiting its durability. It has a basic specific gravity of 0.42 and an average dried weight of approximately 485 kg/m³, with a , even texture and faint growth rings. The wood is notably weak, with a Janka of 720 lbf, and exhibits poor rot resistance, rendering it perishable and susceptible to decay and damage. Historically, Native American communities utilized boxelder wood for various crafts due to its workability. Early Native American peoples in crafted wooden flutes from it, with artifacts dating to 620–670 CE representing the oldest known examples in the Americas. The Cheyenne employed it to fashion bowls, while other groups used it for items like pipestems, drums, and dishes carved from burls and knots. Additionally, it served as fuelwood and for producing charcoal, valued by Plains tribes for ceremonial purposes such as tattooing. In modern contexts, boxelder wood finds primary use in low-value products owing to its lightweight and easily processed nature. It is commonly converted into pulp for paper production and , as well as for manufacturing crates, boxes, and inexpensive furniture. Its weakness precludes structural applications, though it supports turned objects and small ornamental items in . The ' rapid growth rate facilitates sustainable harvesting as a , though its overall commercial value remains limited due to the wood's inferior strength and quality compared to other hardwoods. This positions boxelder more as an opportunistic source in managed forests rather than a high-priority timber species.

Medicinal and Food Uses

Acer negundo, commonly known as boxelder, has been utilized by of for both and medicinal purposes, primarily involving its sap, inner bark, and seeds. The sap, collected in early spring through tapping similar to other maples, can be boiled down to produce a or , though it yields a lower sugar content compared to like sugar maple (). historically processed the sap into sugar, and it served as a during times of scarcity. The inner bark's layer was consumed as a source, particularly during famines, providing a mucilaginous texture. Seeds, produced in small clusters, have been occasionally roasted or boiled after removing the wings, but their low yield and limited nutritional value make them a minor dietary component. Medicinally, the inner bark has been employed by various tribes for its purgative effects. The Ojibwa and used infusions or decoctions of the inner bark as an emetic to induce , often for or to treat ailments like respiratory conditions. These practices reflect a deep cultural integration in North American Indigenous traditions, with limited adoption by , who occasionally used bark washes for skin conditions but did not widely incorporate it into their pharmacopeia. Contemporary research has explored the plant's potential therapeutic value, particularly in its leaves, which contain with properties. A 2020 metabolomic study identified high levels of such as quercetin-3-glucoside and kaempferol-3-O-glucoside in leaf extracts, suggesting applications in nutraceuticals for their free radical-scavenging abilities. However, these findings remain preliminary, and Acer negundo is not approved by regulatory bodies like the FDA for medicinal use. Due to potential toxicity risks, especially from hypoglycin A in the seeds—which can cause muscle damage primarily in and other animals, with possible risk to humans—consumption should be approached with caution and ideally avoided without expert guidance.

References

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