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Acer macrophyllum

Acer macrophyllum, commonly known as bigleaf maple or Oregon maple, is a large tree in the family (formerly Aceraceae), native to the Pacific coastal regions of from to . It is the tallest species of in , typically reaching heights of 15–30 m (50–100 ft) with a diameter of 0.5–1.2 m (20–48 in) and a broad, rounded to irregular canopy that often branches low to the ground. The tree is most notable for its massive, opposite, palmately 5-lobed leaves, which measure 20–36 cm (8–14 in) across— the largest of any species—and are dark green above with a light green, pubescent underside, turning yellow to orange in fall. Small, fragrant greenish-yellow flowers appear in drooping panicles in early spring before the leaves emerge, followed by paired winged samaras 3–5 cm (1–2 in) long that aid in wind dispersal. The bark is smooth and grayish on young trees, becoming reddish-brown and deeply furrowed with age, often supporting epiphytic mosses, lichens, and ferns in humid environments. Native to low- to mid-elevation forests west of the and ranges, A. macrophyllum thrives in cool, moist climates from to about 1,650 m (5,500 ft), particularly in well-drained alluvial or colluvial soils along river bottoms, slopes, and coastal foothills. Its range spans from southwest through , , and into northern and , within roughly 300 km of the , where it tolerates a variety of conditions from wet coastal fog belts to drier inland sites. Ecologically, it is a fast-growing that sprouts vigorously from stumps (up to 3 m per year) and contributes to , while providing and food for , including that eat its seeds and that feed on its foliage. The tree's sap is high in sugar content, supporting limited production of , and its wood is valued for its strength and figure in furniture, musical instruments, and frames. In cultivation, A. macrophyllum is hardy to USDA Zone 6 (and sometimes 5), preferring full sun to partial shade and moist, acidic to neutral soils, though it adapts to urban conditions and is used as a in the . Indigenous peoples of the region have long utilized it for medicinal purposes, crafting paddles from the wood, and harvesting for baskets. Despite its resilience, the species can be susceptible to branch breakage in storms due to its brittle wood, and it faces minor threats from in its native range.

Taxonomy

Nomenclature and etymology

The binomial name Acer macrophyllum was first published by Frederick Traugott Pursh in his 1813 work Flora Americae Septentrionalis, volume 1, page 267, based on specimens collected in the . Pursh, a German-American , described the species from material gathered during and Clark's expedition, establishing it as a distinct member of the maple genus. This naming adheres to the principles of introduced by , with denoting the genus and macrophyllum the specific epithet. The genus name Acer derives from the Latin word for "sharp" or "pointed," originally referring to the hardness and sharpness of maple wood or the pointed lobes of maple leaves, a usage traceable to classical texts. The specific macrophyllum combines the Greek words makros (large) and phyllon (leaf), highlighting the species' distinctive feature of having the largest leaves among North American , often exceeding 25 cm in width. This etymological emphasis on leaf size underscores the tree's morphological prominence in its native habitats. Common names for Acer macrophyllum include bigleaf maple, maple, and broadleaf maple, reflecting its wide leaves and regional prominence along the . In , it is often simply called bigleaf maple, while " maple" is more prevalent in the states of and , where the is a cultural and ecological icon. These names vary slightly by locale but consistently emphasize the leaf morphology. Historically, several synonyms have been proposed for Acer macrophyllum, primarily as infraspecific varieties based on minor or growth form variations, but modern treats the species as monotypic without recognized or varieties. Notable synonyms include Acer macrophyllum var. sinuosum (Rehder) , described in 1920 for with more wavy leaf margins from , and Acer macrophyllum var. kimballi Harrar, proposed in 1946 for a form with denser pubescence; these were synonymized due to insufficient morphological distinction and overlapping variation within populations. Such synonymy reflects ongoing refinements in , prioritizing genetic and ecological continuity over subtle phenotypic differences.

Classification

Acer macrophyllum belongs to the kingdom Plantae, phylum Tracheophyta, class Magnoliopsida, order , and family , reflecting the APG III classification that subsumed the former family Aceraceae into Sapindaceae based on molecular and morphological evidence. The species is placed in the genus , which includes approximately 155 species of deciduous and evergreen trees and shrubs distributed primarily in the . Within Acer, A. macrophyllum is classified in section Macrophylla, a monotypic North American section characterized by large, palmately lobed leaves and racemose inflorescences. Phylogenetic analyses using nuclear loci place section Macrophylla as sister to the Eurasian section Platanoidea, with divergence estimated around 36 million years ago; A. macrophyllum shows closer molecular affinity to Eurasian maples than to other western North American species like circinatum in section Palmata.

Description

Morphology

Acer macrophyllum is a tree that typically reaches heights of 15 to 30 meters and diameters at breast height of 50 to 120 centimeters, forming a broad, rounded crown that can span up to two-thirds of its height in dense stands. It exhibits a shade-tolerant growth habit, often occurring as an species but capable of ascending to the canopy in suitable conditions, with vigorous sprouting after disturbance. Individuals can live up to 300 years, though height growth slows after 50 to 70 years. The bark on young trees is smooth and grayish-brown, transitioning with age to a darker red-brown color with deep furrows, ridges, and scales that often support epiphytes such as mosses and ferns. Leaves are opposite, palmately lobed with 3 to 5 coarsely toothed lobes, measuring 15 to 30 centimeters across (exceptionally up to 61 centimeters), lustrous dark green above and paler beneath, turning yellow to orange in autumn. Petioles are 12 to 25 centimeters long and exude milky sap when broken. Flowers are polygamous, greenish-yellow, fragrant, and small (about 10 millimeters across), borne in pendulous racemes or panicles 10 to 15 centimeters long, blooming from to June before or with emerging leaves. Fruits consist of paired, pubescent samaras 3.5 to 5 centimeters long with horizontally spreading wings in a V-shape, maturing in late summer and ripening to tan or brown from September to October. The is shallow and extensive, with widespreading lateral roots adapted to moist or saturated soils, contributing to its stability in riparian and environments.

Chemistry

The of Acer macrophyllum is characterized by a high content, primarily consisting of , glucose, and , which constitute the majority of its dissolved solids. These carbohydrates typically range from 1.0% to 2.6% of the 's by weight, with an average around 1-1.5% in populations, making it suitable for production despite lower concentrations compared to eastern maple species. The extraction process to produce requires down the to approximately 66% solids, resulting in a of about 80 gallons of to yield 1 gallon of due to the relatively dilute levels. Leaves of A. macrophyllum contain significant levels of , including and , which contribute to the plant's properties. These phenolics are part of a broader profile common in the genus, where they accumulate in foliage to support physiological functions. The and of A. macrophyllum feature lignins, which form a key component of matrix, comprising up to 20-30% of its and aiding in .

Distribution and habitat

Geographic range

Acer macrophyllum is native to western , with its range extending from southern through and the to southwestern , and eastward to isolated populations in western and . The species primarily occurs west of the and mountain ranges, where it is widespread in coastal and inland valleys, including the Coast Ranges, Klamath-Siskiyou Mountains, and foothills of the Cascades and northern . Within its native distribution, Acer macrophyllum occupies elevations from to approximately 1,500 m, though it reaches up to 1,800 m in and higher in southern regions; optimal growth occurs at lower to mid-elevations between 100 and 800 m, where moisture availability supports its development. The has been introduced in limited ornamental plantings outside its native range, including in (such as the and ) and eastern , but it has not achieved widespread naturalization in these areas.

Habitat requirements

Acer macrophyllum thrives in moist, well-drained loamy soils, particularly alluvial and colluvial types with deep, gravelly profiles, though it tolerates clayey and rocky substrates but performs poorly on drought-prone sandy soils. It prefers slightly acidic to neutral levels ranging from 5.5 to 7.5, with average values around 5.5 in sites, and shows sensitivity to toxic levels in . The species favors cool, humid maritime or montane climates typical of the , with annual precipitation ranging from 75 to 250 cm and mild winters corresponding to USDA hardiness zones 6 through 8. Mean annual temperatures vary from 8–15°C, with a frost-free period of 140–350 days, and it endures moderate in southern ranges but requires consistent moisture for optimal growth. Acer macrophyllum is moderately shade-tolerant, commonly occurring in the of forests where it receives 0–20% full for establishment, though it also grows in full sun along riparian zones. It inhabits microhabitats such as streambanks, moist ravines, river terraces, floodplains, and coastal fog belts, often at elevations from to 2,000 m, where abundant moisture and seepage support its development. In associated plant communities, it frequently co-occurs with red alder (Alnus rubra) in riparian zones and with Douglas-fir (Pseudotsuga menziesii) and various oak species (Quercus spp.) in mixed evergreen forests, forming part of cover types like Pacific Douglas-fir and red alder stands on moist to mesic sites.

Ecology

Ecological interactions

Acer macrophyllum is primarily insect-pollinated, with bees, flies, and beetles serving as key vectors that transfer pollen between male and female flowers on the same tree, facilitated by its heterdichogamous flowering system that promotes outcrossing. Flowers emerge in early spring and attract early-season pollinators seeking nectar, contributing to the tree's role in supporting pollinator communities during a period of limited floral resources. While wind may play a minor role in pollen dispersal, insect assistance ensures effective fertilization in its moist forest habitats. Seed dispersal in Acer macrophyllum occurs primarily via , with paired samaras featuring broad wings that enable autorotational flight, allowing seeds to travel up to 100 meters from the parent under favorable conditions. Dispersal typically happens from through , though many seeds remain on branches during this period, extending opportunities for release. such as squirrels and chipmunks interact with these seeds by caching them, which can aid secondary dispersal and burial, though high predation rates often limit successful . Seeds of Acer macrophyllum are a significant source for , including like evening grosbeaks and small mammals such as chipmunks and deer mice, which consume them voraciously and influence through predation. Foliage and twigs provide browse for larger herbivores, notably and , particularly in winter when other forage is scarce, shaping interactions in mixed forests. The also contributes to food webs by supporting communities on its bark and leaves, which in turn serve as prey for insectivorous . Acer macrophyllum offers habitat value, providing nesting sites and cover for various , including pileated woodpeckers that excavate cavities in its soft wood and like barred owls that utilize mature stands for roosting and . Its expansive canopy and branching structure create microhabitats for small mammals and amphibians, enhancing in riparian and upland forests. The species forms symbiotic associations with arbuscular mycorrhizal fungi, particularly vesicular-arbuscular types, which colonize its and enhance nutrient uptake, especially , in nutrient-poor soils common to its habitats. These fungi also extend to adventitious in canopy soils of old-growth trees, facilitating acquisition in epiphytic environments. Additionally, Acer macrophyllum supports epiphytic communities, including mosses, liverworts, ferns, and clubmosses like species, whose growth on its is promoted by the tree's moisture-retaining texture and shaded . In forest dynamics, Acer macrophyllum acts as a in disturbed riparian areas, rapidly colonizing flood-scoured banks or post-fire sites following early successors like and willows. Through leaf litter , it facilitates by increasing retention and nutrient cycling, creating conditions suitable for later-seral and plants in moist ecosystems. Its presence in mid-seral stages helps stabilize riparian zones, reducing erosion and supporting diverse plant assemblages.

Pests and diseases

Aphids of the genus Periphyllus, such as P. lyropictus and P. testudinaceus, are common pests on Acer macrophyllum, feeding on sap and causing leaf curl, distortion, and honeydew production that promotes sooty mold growth. These aphids are most active in spring, with populations peaking before winged forms migrate, though they rarely cause severe damage to mature trees in natural settings. Borers such as the flatheaded appletree borer (Chrysobothris femorata) attack stressed or wounded trees, tunneling into the bark and to weaken structural integrity and facilitate secondary infections. Among fungal diseases, , caused by Verticillium dahliae, can affect maples by blocking , resulting in wilting branches and dieback. Anthracnose, primarily from Aureobasidium apocryptum (syn. Discula spp.), emerges in wet springs, producing irregular leaf spots along veins that lead to premature defoliation but typically do not kill the tree. Heart rot in mature trees is often induced by Ganoderma applanatum, entering through wounds to decay heartwood and compromise stability over time. Root rot from species occurs in poorly drained, wet soils, causing root decay, crown decline, and increased susceptibility to toppling. Since around 2011, widespread decline and dieback of A. macrophyllum has been observed across its range in and , with possible extension into . This multifactorial issue is associated with abiotic stressors including rising summer temperatures, , urban development, , and contaminants such as and , rather than a single biotic agent. Secondary pests and diseases may contribute under stress, but no primary has been identified; for example, partial defoliation by the redhumped caterpillar (Schizura concinna) was reported in as of 2024. In its native range, biotic pests and diseases rarely prove fatal to healthy trees, allowing recovery through refoliation; however, trees in face heightened vulnerability due to stressors like transplant shock and .

Conservation status

_Acer macrophyllum is classified as Least Concern on the , with the most recent assessment conducted in 2017 and no subsequent updates as of 2025. NatureServe assigns it a global rank of G5, indicating the species is demonstrably secure globally due to its wide distribution and abundance. Subnational ranks are similarly secure, including N5 in both and the , with S5 in and . The species maintains abundant populations across its core range in the , where it occupies extensive forested landscapes spanning millions of s in coastal and inland regions from to . In riparian zones, which represent optimal habitat, population densities typically range from 50 to 200 stems per , particularly in early seral stages following disturbance. These densities reflect the 's prevalence in moist, low-elevation sites, though they vary with successional stage and site conditions. Overall population trends are stable, with increases observed in protected areas where disturbances are managed. Local declines have occurred in some regions due to historical , but the exhibits strong regeneration through and establishment post-disturbance. Age structure is skewed toward mature individuals, largely attributable to suppression practices that reduce opportunities for regeneration while allowing established s to persist. Monitoring efforts by the USDA Forest Service, including data from the Forest Inventory and Analysis program, indicate no significant range contraction for Acer macrophyllum since 2000, supporting its continued abundance within the native .

Threats

Habitat loss poses a significant threat to Acer macrophyllum, particularly through historical and ongoing in riparian zones, which has reduced suitable moist habitats across its in the . In , riparian forests dominated by bigleaf maple experienced substantial degradation from timber harvest practices prior to the late , leading to fragmentation and loss of mature stands that support the ' regeneration. Urbanization in has further exacerbated this, with development encroaching on native habitats and increasing decline rates near impervious surfaces and , where symptoms of stress are more prevalent. Climate change intensifies drought stress on A. macrophyllum, especially in the southern portion of its range, where reduced moisture availability limits growth and survival in increasingly arid conditions. Projections indicate potential contraction of suitable habitat in the southern portion of its range due to altered precipitation patterns and higher temperatures. Recent declines in western Washington have been linked to abiotic stresses like heat and drought, correlating with warmer, drier summers that impair transpiration and photosynthesis. Invasive species contribute to competitive pressures on A. macrophyllum, with non-native plants like Himalayan blackberry (Rubus armeniacus) invading disturbed riparian understories and outcompeting seedlings for light and nutrients in the . Additionally, the tree facilitates establishment of invasive barred owls (Strix varia), which preferentially nest in uneven-aged bigleaf maple stands, indirectly altering forest dynamics through associated ecosystem changes. Alterations to natural fire regimes, primarily through suppression, favor coniferous competitors over A. macrophyllum by allowing denser shade-tolerant overstories to develop, reducing opportunities for maple regeneration in mixed forests. , including nutrient runoff and sediment from adjacent farmlands, degrades riparian , stressing bigleaf maple in lowland zones dependent on clean . Mitigation efforts include protection within federal lands, including national forests such as the Willamette and Siuslaw National Forests, providing refugia from and . Overall, A. macrophyllum holds a secure conservation ranking (G5 globally), though local populations face ongoing risks from these pressures.

Cultivation

Propagation

Acer macrophyllum is primarily propagated from seeds, which are collected as in the fall from to using tools such as pole pruners to reach upper branches. Freshly collected seeds should be stored in plastic bags under cold conditions to maintain viability, as they have a short and can decay quickly if not handled properly; viability can last up to one year at 1°C with low moisture content of 10-20%. For , seeds require cold stratification at 3°C for a minimum of 50 days, ideally 60-90 days, to overcome , followed by in under moist, shaded conditions. Sowing involves placing one seed per container (such as 1-4 gallon Treepots) in a well-draining mix like peat-based , with the samara wing oriented vertically, and maintaining temperatures around 15°C for optimal rates of 30-40%, which can reach up to 80% in protected settings. is and typically occurs from late January to May, with site preparation emphasizing moist, shaded areas to mimic natural conditions. Vegetative propagation is less common but feasible through stem cuttings from young shoots or coppicing, where stumps produce vigorous sprouts after cutting, allowing for clonal reproduction in cultivation. Rooting success from cuttings can be achieved when taken from juvenile material and treated with rooting hormones, though bigleaf maple does not readily layer like related species such as vine maple. Grafting onto compatible rootstocks, such as those from other Acer species, is used for specific selections, providing a method to maintain desirable traits while improving adaptability. In cultivation, Acer macrophyllum thrives in USDA hardiness zones (5)6, preferring well-drained, moist soils with 4.8-7.0 and partial shade to full sun. Maturity, marked by production, is reached in 10-15 years under favorable conditions, with optimal summer temperatures around 30°C and cooler winters of 3-19°C supporting steady growth. Challenges in include slow juvenile in the first year, particularly when competing is present, which can limit establishment to low rates without site clearing. Additionally, the is susceptible to transplant shock due to its shallow , necessitating careful handling during outplanting, such as using plantable and providing and consistent to minimize mortality. In natural settings, wind-dispersed and stump contribute to , informing cultivated techniques that emphasize protection from predators and environmental stress.

Cultivars

Several notable cultivars of Acer macrophyllum have been selected and introduced primarily by nurseries in the , focusing on enhanced ornamental qualities such as distinctive foliage coloration, , and growth habit suitable for use. These selections often emphasize vibrant or fall colors and more compact forms compared to , while maintaining similar hardiness in USDA zones (5)–6. One popular cultivar is 'Mocha Rose', a Buchholz Nursery selection discovered in Oregon, known for its striking new spring foliage emerging in shades of peach-pink to pinkish-red with yellow veins, transitioning to mocha-rose or dusky-purple tones before maturing to bronze-green in summer. Fall color includes orange-browns and yellows, adding seasonal interest. This cultivar grows to about 15–20 feet tall and 18 feet wide with a spreading habit, making it suitable for smaller gardens. 'Santiam Snows' is a rare variegated form discovered as a wild clone along the Santiam River in and introduced by Heritage Seedlings, featuring large leaves randomly splashed and speckled with white patches against a background for a striking, snow-like effect. Its compact growth habit supports urban planting applications, where the bold provides visual contrast without the full size of the species. 'Seattle Sentinel' offers a narrow, columnar form, selected from a street tree in and named in 1951 by Brian Mulligan, former director of the Washington Park Arboretum. This upright cultivar reaches up to 12 meters (40 feet) in height with dense, erect branching, ideal for confined spaces or as a vertical accent in landscapes. These cultivars are widely available through specialty nurseries in the , often propagated via to preserve their unique traits, and share the species' tolerance for moist, cool conditions in the .

Uses

Traditional uses

Native American tribes of the and have long utilized Acer macrophyllum, known as bigleaf , for various traditional purposes, with documentation appearing in ethnobotanical studies from the late 19th and early 20th centuries. Tribes such as the Clallam collected and consumed the tree's sap fresh or dried, boiling it down to produce a or sugar-like substance, though yields were lower than those from eastern sugar maples. from the inner bark was eaten raw or with oil by peoples, providing a nutritious layer during spring. Medicinally, the bark's high content made it valuable for its properties; tribes like the Klallam prepared infusions or teas from the inner bark to treat sore throats, , and gastrointestinal issues such as . The raw sap served as a general tonic among the , aiding overall vitality. For material uses, the flexible inner bark provided strong fibers ideal for crafting; the Cowlitz and Concow twisted it into cordage for ropes and tumplines, while the and others wove it into baskets during when it was most pliable. The wood, lightweight yet durable, was prized for tool handles, utensils, and carvings—Northwest Coast tribes including the Haida, Kwakiutl, and Nitinaht shaped it into paddles, spoons, dishes, and whorls, earning it the name "paddle " in several languages. Large leaves lined baskets, wrapped fish for storage, or covered foods in earth ovens among the Cowichan and . Culturally, A. macrophyllum held significance in Northwest Coast traditions, with the Kwakiutl and Nitinaht carving the wood into ceremonial masks and rattles for rituals and performances. These practices were first systematically recorded in 19th-century ethnographies, highlighting the tree's integral role in indigenous economies and ceremonies.

Commercial uses

Acer macrophyllum is widely utilized as an ornamental tree in , particularly valued for providing substantial shade in large landscapes, parks, and urban settings along the . Its large, deeply lobed leaves offer dense canopy coverage during the , while the foliage turns vibrant shades of yellow and orange in autumn, enhancing aesthetic appeal in regions like the . In cities such as , it has been planted as a street tree due to its upright growth habit and tolerance to urban conditions, though its propensity for litter from large leaves may limit broader use in built environments. The species supports small-scale syrup production through sap tapping, primarily as a hobbyist or artisanal endeavor in and , where it is marketed under names like " maple syrup" or "bigleaf maple syrup." Mature trees can yield 11 to 23 liters of sap per season under typical conditions, with content ranging from 1.0 to 2.6 percent, requiring approximately 80 gallons of sap to produce one gallon of —double the volume needed for maple. This lower yield and milder flavor profile restrict large-scale commercial operations, but emerging interest has led to vacuum-assisted systems and processing for efficiency in limited production. Beyond ornamentals and , A. macrophyllum serves as a supplementary source for , with its foliage and young stems browsed by and other animals in forested pastures. of A. macrophyllum is commercially important in the , where it is harvested for furniture, veneer, paneling, hardwood plywood, musical instruments, flooring, frames, turned objects, and . Its light color, fine texture, and occasional figuring make it suitable for specialty items like boxes, crates, and novelties. Ornamental specimens are commercially available through numerous nurseries in the , supporting sales for residential and public projects. Sustainable harvesting practices for from the species occur in Forest Stewardship Council (FSC)-certified forests in and , ensuring environmentally responsible management of stands.

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