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Schefflera

Schefflera is a of flowering in the family , comprising approximately 600 species of mostly evergreen trees, shrubs, and lianas distributed throughout tropical and subtropical regions of , , the southwest Pacific, the Neotropics, , and . Commonly known as trees or plants for their distinctive whorled or digitate compound leaves that radiate from the petiole like the ribs of an open , many species feature palmately arranged leaflets numbering from 3 to over 20, with small, inconspicuous flowers clustered in umbels or compound panicles, and followed by fleshy, berry-like drupes. The genus, named after the 18th-century German physician and botanist Johann Peter Ernst von Scheffler, was traditionally the largest in and has significant ornamental value, with species such as (formerly Schefflera actinophylla) and (formerly Schefflera arboricola) widely cultivated as durable houseplants in temperate regions. However, recent phylogenetic analyses have demonstrated that Schefflera sensu lato (s.l.)—the traditional broad circumscription—is polyphyletic, encompassing at least five unrelated clades and prompting the transfer of hundreds of species to segregate genera including Heptapleurum, Plerandra, and Sciadophyllum; consequently, Schefflera sensu stricto (s.s.) is now restricted to around 13 species primarily endemic to and the southwestern Pacific islands. Beyond , numerous species formerly placed in Schefflera play roles in across their native habitats, employed for treating conditions such as , , , liver disorders, skin ailments, respiratory infections, , , and even cancer, with phytochemical studies revealing bioactive compounds like triterpenoids, , and essential oils. Ecologically, these often inhabit rainforests, montane forests, and disturbed areas, contributing to in humid , though some, like (formerly S. actinophylla), have become invasive weeds in introduced ranges such as and parts of the .

Taxonomy

Etymology

The genus name Schefflera is pronounced /ˈʃɛflərə/. It was established in 1776 by the botanists and in their publication Characteres Generum Plantarum, honoring Johann Peter Ernst von Scheffler (1739–c. 1809), a and based in who contributed plant specimens to regional floras such as Gottfried Reyger's Tentamen Florae Gedanensis. The Forsters proposed the name during their documentation of plants collected on Captain James Cook's second voyage to the , reflecting Scheffler's contemporary influence in European despite his work being centered in .

Taxonomic History

The genus Schefflera was first described in 1776 by and George Forster, based on specimens of S. digitata collected during James Cook's second voyage to the Pacific, specifically from . This initial circumscription was narrow, encompassing only a few with palmately compound leaves and simple umbellate inflorescences characteristic of the type. During the 19th and early 20th centuries, the genus underwent significant expansion through broad interpretations by taxonomists such as Henri Baillon (1878–1879), who incorporated segregate genera like Agalma, Brassaia, and Heptapleurum, and Hermann Harms (1894–1897), who formalized subsections such as Euschefflera and Cephaloschefflera. By the mid-20th century, David Frodin (1975) further consolidated the taxonomy, reducing many segregates and proposing 16 informal groups, which contributed to an inflated estimate of over 600 species distributed pantropically by the late 20th century. This wide circumscription reflected morphological similarities in leaf and inflorescence structure but overlooked underlying evolutionary divergences. The polyphyletic nature of Schefflera sensu lato began to emerge in the through morphological analyses highlighting inconsistencies in traditional groupings, but it was definitively demonstrated in the early using molecular data. Phylogenetic studies by Plunkett et al. (2004, published 2005) analyzed ITS and trnL-trnF sequences from over 100 species, revealing Schefflera as embedded within five distinct, non-monophyletic clades scattered across the family, corresponding roughly to southwest Pacific, Neotropical, Asian/Malesian, /Malagasy, and a core Australasian group. Subsequent work by Plunkett et al. (2018) refined these findings with expanded sampling and multi-locus data, confirming the deep and aligning clades more closely with biogeographic patterns than alone. These insights prompted major taxonomic revisions from the onward to achieve monophyletic genera. In the Pacific clade, species were reassigned to Plerandra (Lowry et al., 2013), accommodating about 20 New Caledonian endemics previously under Schefflera. For the Asian and clade, including popular houseplants like S. arboricola, the genus Heptapleurum was resurrected in 2020 to include over 300 , emphasizing tricarpellate ovaries and palmate leaves as synapomorphies. In the Neotropics, the Didymopanax group—comprising 37 with bicarpellate gynoecia—was formally resurrected as Didymopanax Decne. & Planch. in 2020, marking a significant post-2010 shift from the broader Schefflera concept. These reclassifications, building on Plunkett's phylogenetic framework, have reduced Schefflera sensu stricto to around 13 Australasian while addressing longstanding taxonomic instability.

Current Classification

Schefflera is classified within the subfamily Aralioideae of the family , order . Molecular phylogenetic analyses place the genus in the Australasian of Aralioideae. Following extensive taxonomic revisions, Schefflera is now restricted to 13 accepted , all endemic to and the southwestern Pacific (including , , , , and ), excluding former broad tropical elements reassigned to other genera. As of November 2025, accepts 13 in the genus. These boundaries were established through initial generic splits proposed by Frodin in his 2004 world checklist of , which highlighted the of the traditional circumscription. Subsequent work by et al. in 2020 reassigned Neotropical species to resurrected genera such as Didymopanax and Sciodaphyllum, further refining the scope. No significant alterations to this classification have occurred since , as reflected in updated floras and databases like .

Description

Habit and Morphology

Schefflera plants are shrubs or small trees up to 10 m in height, typically with an unarmed woody architecture and multiple stems arising from the base, contributing to a bushy or spreading silhouette in mature individuals. The bark is smooth and greenish in younger stems, becoming fissured and grayish-brown in older growth. Stems are erect, cylindrical to slightly angled, with prominent raised scars marking former petioles, giving branches a ringed appearance. Larger tree forms may produce shallow buttresses at the base for stability. The leaves are arranged alternately along the stems in a palmately configuration radiating outward like an , typically comprising 5-12 digitate leaflets per . These leaflets are leathery, measuring 5-15 cm in length and 2-5 cm in width, with toothed margins and a glossy dark green upper surface. Petioles are robust, 10-30 cm long, with sheathing bases, and leaves often form rosette-like clusters at branch tips.

Flowers, Fruits, and Reproduction

The flowers of Schefflera species are small, typically unisexual (with some species dioecious), measuring 3–5 mm in , with a greenish-white coloration. They are arranged in terminal or axillary umbels forming compound panicles up to 30 cm in length. Each flower features 5 sepals that are reduced and triangular, 5 free petals, and an equal number of stamens inserted on a short surrounding a semi-inferior with 5 locules. Pollination occurs primarily through . Flowering is seasonal in native ranges. The fruits are globose drupes, approximately 4–6 mm in diameter, ripening to black and containing 5 stony pyrenes, each enclosing a single . Fruits are dispersed primarily by .

Distribution and Habitat

Geographic Range

Schefflera species are native to and various islands in the southwestern , reflecting the genus's restriction to an Australo-Pacific clade following recent taxonomic revisions. In , the genus is represented by species such as S. digitata, which is endemic and widespread across the , , and [Stewart Island](/page/Stewart Island). The native distribution extends to subtropical and temperate Pacific regions, including , , , and , where the 13 accepted species are primarily confined, with several endemics in New Caledonia. This range underscores the genus's concentration in isolated island ecosystems, with no native occurrences beyond these areas in the current classification. Some Schefflera species have been introduced sparingly as ornamentals in climatically similar regions, such as parts of and , though none have become widespread invasives within the restricted genus. Fossil records from strata indicate a historically broader distribution across eastern and southeastern and the Pacific, extending the genus's ancient range beyond its modern limits.

Ecological Preferences

Schefflera species predominantly inhabit moist, well-drained soils within lowland to montane rainforests, typically at elevations ranging from 0 to 1500 meters, where they often occupy positions or edges of the canopy. These environments provide the humid, shaded conditions favored by the genus, with some extending into swamp forests, scrub, thickets, and disturbed areas across subtropical and temperate regions. The genus exhibits notable tolerances to varying light levels, thriving in shade to partial sun, which suits their role as plants with leathery leaves adapted for low-light persistence. Temperature tolerances vary by species; for instance, Schefflera digitata withstands moderate frosts down to approximately -10°C in its native habitats, while species from tropical Pacific islands prefer warmer conditions. Many are wind-resistant due to sturdy branching and can grow as epiphytes or lithophytes, enhancing their adaptability to rocky or arboreal substrates. Ecologically, Schefflera acts as a in forest gaps, facilitating regeneration by stabilizing soil and providing initial cover, while offering and for epiphytes, insects, and ; their fruits are primarily dispersed by frugivores such as parrots and pigeons. Major threats to Schefflera include habitat loss from , , , and fires—exacerbated by climate change-induced droughts—as well as competition from in altered ecosystems. While IUCN assessments are limited for most , some Pacific island endemics are due to lack of recent observations.

Species Diversity

Accepted Species

The genus Schefflera is currently recognized as comprising 13 accepted , following recent taxonomic revisions that restricted it to a monophyletic endemic to the southwestern Pacific region. These exhibit high , with distributions confined to isolated island groups such as (hosting the majority), , , , and (with a single ). They are typically trees or shrubs with palmate compound leaves, adapted to humid, forested habitats, and distinguished by variations in leaflet number, margin type, and structure.
  • Schefflera balansana Baill.: This tree is endemic to New Caledonia, where it inhabits wet tropical forests; it is characterized by palmate leaves with 5–7 oblong leaflets that have entire margins and a tree habit reaching up to 10 m tall.
  • Schefflera candelabrum Baill.: Native exclusively to New Caledonia, this species forms trees in humid tropical environments and is notable for its robust, candelabra-branched habit and compound leaves with 7–9 broadly elliptic leaflets.
  • Schefflera coenosa (R.Vig.) Frodin: Endemic to southeastern New Caledonia, including the Isle of Pines, it is a tree of wet tropical biomes distinguished by densely clustered inflorescences and leaves with 5–7 lanceolate leaflets.
  • Schefflera digitata J.R.Forst. & G.Forst.: The sole species in New Zealand, occurring throughout both main islands in lowland to montane forests up to 1200 m; it is a small tree up to 10 m tall with distinctive palmate leaves bearing 7–10 serrate-margined leaflets.
  • Schefflera euthytricha A.C.Sm.: Restricted to Fiji, this tree grows in wet tropical forests and features straight-stalked (euthytrichous) pedicels supporting umbellate inflorescences, with leaves comprising 7–11 elliptic leaflets.
  • Schefflera kerchoveana (Veitch ex W.Richards) Frodin & Lowry: Endemic to New Caledonia, it is a shrubby tree in tropical wet habitats, recognized by its finely pubescent branches and leaves with 5–7 ovate leaflets that are glabrous above.
  • Schefflera leratii R.Vig.: Native to New Caledonia, this species inhabits humid forests as a tree with slender branches; it is distinguished by its elongated racemose inflorescences and leaves having 7–9 narrowly elliptic leaflets with acute tips.
  • Schefflera neoebudica Guillaumin: Found only on Vanuatu (New Hebrides), it is a tree of wet tropical biomes featuring robust stems and compound leaves with 5–7 obovate leaflets that are prominently veined.
  • Schefflera ouveana (Däniker) Frodin: Endemic to the Loyalty Islands of New Caledonia, this tree occurs in coastal wet forests and is characterized by its salt-tolerant habit, with leaves of 5–7 coriaceous, elliptic leaflets.
  • Schefflera pseudocandelabrum R.Vig.: Restricted to New Caledonia, it grows as a tree in tropical rainforests, resembling S. candelabrum but differing in its less branched inflorescences and leaves with 7–9 slightly toothed leaflets.
  • Schefflera samoensis Rehd.: Native to Samoa and nearby Pacific islands, this species is a canopy tree in wet montane forests, notable for its large panicles and leaves with 9–13 long-acuminate leaflets.
  • Schefflera vieillardii (Baill.) R.Vig.: Endemic to New Caledonia, it is a tree of ultramafic soils in humid areas, distinguished by its villous indumentum on young parts and leaves with 5–7 broadly ovate, tomentose leaflets.
  • Schefflera vitiensis (Seem.) R.Vig.: Confined to Fiji (Viti Levu), this tree inhabits ridge forests in wet tropics and features compact umbels with leaves comprising 7–9 elliptic-oblong leaflets that are glabrous and leathery.

Synonymized or Transferred Species

Molecular phylogenetic studies have demonstrated that Schefflera, as traditionally circumscribed, is polyphyletic, with its species distributed across multiple distant clades within the family. This realization has prompted extensive taxonomic revisions, resulting in the reassignment of approximately 600 previously included in Schefflera to other genera (as of 2020). As of 2025, further refinements continue, with over 320 in Heptapleurum alone. These transfers are primarily driven by DNA sequence data from nuclear and plastid markers, which reveal deep evolutionary divergences unsupported by morphological similarities alone. One major revision involves the Asian , where over 320 (as of 2025) were transferred to the resurrected genus Heptapleurum Gaertn. in , based on its distinct phylogenetic position nested within but separate from the core Schefflera lineage. Notable examples include (Hayata) Lowry & G.M.Plunk. (formerly Schefflera arboricola (Hayata) Merr.), a popular dwarf umbrella houseplant native to and southern , widely cultivated for its compact form and ornamental foliage. Another is (Endl.) Lowry & G.M.Plunk. (formerly Schefflera actinophylla (Endl.) Harms), known as the Queensland umbrella tree, an often grown as a street tree for its striking, radiating leaf clusters. Additional transfers encompass Heptapleurum heptaphyllum (L.f.) Blume (formerly Schefflera heptaphylla (L.f.) Frodin), a widespread Indo-Malayan valued in . In the Neotropics, revisions have fragmented the former Schefflera diversity into several genera, reflecting geographically and morphologically coherent clades identified through phylogenetic analyses. The largest such group is Sciodaphyllum P.Browne, resurrected in 2019 to include around 146 species (as of 2025), primarily from Central and , distinguished by features like globose capitula in their inflorescences. Examples include Sciodaphyllum sprucei (Marchal) Lowry et al. (formerly Schefflera sprucei (Marchal) Frodin), an Amazonian species with distinctive wood . Similarly, the genus Didymopanax Decne. & Planch. was resurrected in 2020 for around 37 species (subject to ongoing transfers), mainly Brazilian, characterized by variable gynoecial structures. A representative case is Didymopanax morototoni (Aubl.) Decne. & Planch. (formerly Schefflera morototoni (Aubl.) Maguire, Steyerm. & Frodin), a widespread Neotropical timber known as cabrite or yagrumo macho. These reclassifications have significant implications for and , as many transferred remain commercially labeled under their original Schefflera names to maintain familiarity among growers and consumers, despite the updated taxonomy. The shifts underscore the ongoing refinement of , prioritizing monophyletic groupings over historical convenience, with new additions (e.g., in Heptapleurum) as recent as 2025.

Cultivation and Uses

Following recent taxonomic revisions, cultivation and uses of Schefflera s.s. focus on its approximately 13 accepted , primarily endemic to and the southwestern Pacific; many popular examples previously classified in Schefflera are now in segregate genera like Heptapleurum, though their care requirements often overlap.

Cultivation Practices

Schefflera are typically propagated by , stem cuttings, or air layering, with spring being the optimal season for initiating these methods to leverage active growth periods. require fresh collection and sowing in a well-draining seed-starting mix, often with pretreatment such as de-pulping for species like S. digitata and cool-moist for 1–2 months to improve rates. Stem cuttings, taken from healthy semi-ripe growth, root best when dipped in rooting hormone and placed in a moist, well-draining medium under high humidity and indirect light, while air layering is effective for larger specimens to encourage root development on intact branches. Cultivation requirements for Schefflera s.s. species, such as S. digitata, emphasize warm, humid environments with temperatures between 10–25°C (50–77°F) in native ranges, partial shade to full sun exposure, and consistently moist but well-drained to prevent waterlogging. These species thrive in USDA hardiness zones 9–11, tolerating a range of soil types from sandy to clay if drainage is adequate, with moderate once established but preferring regular watering during active growth; they exhibit greater cold tolerance (down to ~0°C) compared to tropical segregates. Fertilization with a balanced, slow-release formula every 4–6 weeks in the supports vigorous development, and should be pruned to maintain shape and encourage bushier growth. Note that requirements for species formerly classified under Schefflera (now in genera like Heptapleurum) overlap but are tuned for warmer conditions (15–25°C, zones 10–12). In native contexts, such as gardens, S. digitata is commonly cultivated as a or shelter in moist, sheltered sites with good , leveraging its fast growth and tolerance to wind and partial shade for and enhancement. Common pests include scale , which can be managed through horticultural oils or insecticidal soaps applied to affected leaves and stems, while —often caused by overwatering or poor —is prevented by using pots or beds with ample drainage holes and allowing the topsoil to dry slightly between waterings.

Traditional and Modern Uses

Schefflera species have been utilized by in traditional practices, particularly in and other Pacific regions. In , Schefflera digitata, known as patē or patatē, has been employed for medicinal purposes, with leaves applied as poultices to treat skin complaints such as ringworm and sores, owing to the presence of falcarindiol, a compound with properties. The sap has been used topically for ringworm, scrofula, and , while berries provided a and writing ink. Additionally, the wood served practical roles, including fire-starting by and crafting tools like sockets and (throwing spears), reflecting its value among Pacific islanders for utilitarian purposes. In contemporary contexts, Schefflera s.s. species like S. digitata are valued as ornamental plants in landscaping, where they form hedges, screens, and accents in gardens, particularly in native plantings. Species formerly classified in Schefflera, such as and H. arboricola, are widely cultivated for their lush foliage in tropical and indoor settings. They play a minor role as timber sources in some regions, though not a major economic contributor. Recent research on Schefflera s.l. highlights potential, particularly triterpenoids isolated from various species, which exhibit effects and warrant further pharmacological exploration, as summarized in a 2021 review. Horticultural applications often involve species previously or currently classified within Schefflera, underscoring the genus's limited but notable role beyond traditional uses.

Paleontological Record

Known Fossil Species

The primary known fossil species attributed to Schefflera s.l. is †S. dorofeevii Łańcucka-Środoniowa, described from fruit compression fossils recovered from Middle Miocene (ca. 15–13 Ma) freshwater sedimentary deposits in the Polish Carpathians. These fossils, consisting of two endocarp specimens, were extracted from borehole samples at depths of 314–319 m in the Nowy Sącz Basin (localities Nowy Sącz I and Chyżne), West Carpathians, Poland. The endocarps exhibit an elongated shape, extremely thin walls, a smooth and flat surface, and subtle longitudinal striations, preserved as compressions in fine-grained sedimentary layers. This morphology closely resembles the fruit structure seen in extant Schefflera species bearing umbellate inflorescences. The discovery of †S. dorofeevii documents the genus's presence in Laurasian paleofloras during the , with subsequent reports confirming its occurrence in late –early deposits of the Tetta Clay Pit, , (Cottbus Formation), based on similarly preserved endocarps (specimen MZ VII/134/264).

Evolutionary Implications

The fossil record of Schefflera s.l. and closely related genera within reveals a historically broader distribution during the Eocene to epochs, extending across both hemispheres and including northern temperate regions, prior to the genus's modern restriction primarily to tropical and subtropical areas of the Southern Pacific, , and the Neotropics. For instance, Osmoxylon-like fossils from the early Eocene of , , represent the earliest direct evidence of in , supporting the family's hypothesized origins on the and subsequent northward dispersal via boreotropical migration routes during the greenhouse climate. Similarly, early fossils of Astropanax (a genus resurrected from former Schefflera species) from indicate a presence in , aligning with the family's expansion into the amid warming periods. These paleontological findings underscore the ancient diversification of , with Schefflera s.l. exhibiting that traces back to pre-Miocene splits among its major clades, such as the Asian (now largely Heptapleurum), Neotropical, and Australasian lineages. Molecular phylogenies calibrated with Eocene fossils suggest that crown-group arose around 45 million years ago (Middle Eocene) with ancestral distribution in . Fossils attributed to Schefflera s.l. from the of the Kodor River in the (S. colchica, S. integrifolia, and S. pontica) further attest to this northern extension, occurring in a subtropical flora before the Pleistocene glaciation, though their placement requires reevaluation under modern . The scarcity of confirmed Schefflera s.l. fossils younger than the suggests a range contraction in higher latitudes during the late , potentially linked to climatic changes.

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