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Rachael Collings (2025)
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Collings, R.J. (2025), 'Tetrapanax papyrifer' from the website Trees and Shrubs Online (treesandshrubsonline.
A fast-growing, thicket-forming, rhizomatous large shrub or small tree to 3.5 m tall, with a slender trunk to c. 9 cm in diameter. Trunk sparsely branched, with stout shoots covered in dusty brown-orange tomentum when young. Mature bark light brown, slightly furrowed; pith large, white and uniform. Leaves simple, large, 50–75 cm across at maturity, alternately arranged, evergreen in milder climates, deciduous when exposed to frosts; palmate, deeply lobed (7–11 ovate-oblong lobes), with some of the larger lobes forked; base obtuse to cordate, apex acuminate, margins entire to coarsely serrate; upper surface green, glabrous, subcoriaceous or thick-papery, lower surface densely ferruginous or stellate-tomentose; palmate venation. Petioles long, 50–75 cm at maturity, terete, glabrous, sheathing at the base, with 2 slender-pointed, prominent stipules which leave conspicuous scars. Infloresence terminal, large, to 90 cm, erect, paniculate, hermaphroditic or andromonoecious, yellow-white flowers on 1–1.5 cm unarticulated pedicels, in racemosely arranged umbellule units 1–2 cm in diameter, not significantly scented, although sometimes reported as honey-scented. Calyx 1 mm, nearly entire or obsolete, densely stellate-tomentose; corolla petals valvate and free, 4–5 × 2 mm, densely stellate-tomentose, stamens 4–5, filaments 3 mm; ovary inferior, carpels 2. Drupaceous fruit 4 mm in diameter, globose, almost glabrous, dark purple-black at maturity, somewhat compressed laterally. Flowering October to December in the temperate northern hemisphere, flowers often damaged by frost in cultivation, fruiting January to February in warmer areas. (Xiang & Lowry 2007; Mourad 2013; Zanlorenzi et al. 2023; Bramley, Trias-Blasi & Wilford 2023; Frodin et al. 2003; Edwards & Marshall 2019; Plunkett et al. 2018).
Distribution China Anhui, Fujian, Guangdong, Guangxi, Guizhou, Hubei, Hunan, Jiangxi, Shaanxi, SW Sichuan, NW Yunnan, Zhejiang Taiwan
Habitat Warm temperate to subtropical forest in mixed thickets 100–2800 m asl, where rainfall is abundant but unevenly distributed throughout the year.
USDA Hardiness Zone 8-10
RHS Hardiness Rating H3
Awards AGM
Conservation status Least concern (LC)
Taxonomic note The ongoing taxonomic difficulties within Araliaceae are discussed briefly in the genus article; for a discussion of the various historical treatments see Frodin et al. (2003). For the present, however, Tetrapanax papyrifer is considered unlikely to change position.
Tetrapanax papyrifer first came to the attention of western botanists in the guise of artificial flowers and watercolour paintings created from ‘rice paper’ (the species epithet papyrifer means ‘paper bearing’ in Latin). These items were popular souvenirs for European travellers in China at the beginning of the 19th century, where the earliest mention of pith paper is thought to be from the Tsin Dynasty (245–420 AD); it was also listed in the Chinese Materia Medica in 1590 and has traditionally been used in Chinese medicine (Nesbitt, Prosser & Williams 2010; Harvard University Herbaria and Libraries 2025). Although botanists realised that the rice paper was not made from rice, it took several decades to identify the plant that provided the raw material. A very interesting detailed account of the pith paper trade is given by Nesbitt, Prosser & Williams (2010).
In 1830, William Jackson Hooker received a sample of the plant whilst Chair of Botany at the University of Glasgow, and wrote to his contacts for identification. It was mis-identified as Aeschynomene aspera (Fabaceae, whose pith is also valued, including for the manufacture of ‘pith helmets’), which perpetuated confusion in the literature for several years (Perdue & Kraebel 1961; Nesbitt, Prosser & Williams 2010). Hooker was tenacious in his quest, and after the First Opium War (1839–42) new opportunities opened up for Western contacts, leading to the discovery of the plant’s origins in the forests of northern Taiwan. Hooker was able to describe the plant as a new species in 1852, which he provisionally named Aralia papyrifer. The acquisition of living plants was hampered by the dangers encountered whilst collecting it, and the problems of transport: keeping the plant alive for long periods on board ships was fraught with difficulties ranging from brown ants to pirates (Hooker 1852)! Finally, two living plants arrived in Britain and flowered under glass in ‘a damp stove’ at Kew in December 1855 (Hooker 1856). It became evident that it differed from Aralia and it was separated into Tetrapanax by Carl Koch in 1859. Bentham and Hooker published it as Fatsia papyrifer (Hook.) Miq. ex Witte. in 1867, under which name it was known for much of the remainder of the 19th century (Nesbitt, Prosser & Williams 2010). It has also historically been placed in Panax, Didymopanax, and Echinopanax (Plants of the World Online 2020).
In the latter half of the 19th century it appears that Tetrapanax papyrifer was somewhat forgotten, as a preference emerged for more compact Araliaceae with interesting juvenile or variegated foliage; however, changing horticultural tastes and unfavourable economic circumstances marked a general downturn for the family’s horticultural fortunes (Frodin et al. 2003). Western perceptions of the exotic allure of China had waned and the rice paper trade declined (Nesbitt, Prosser & Williams 2010), and Tetrapanax papyrifer was considered too tender to be treated in Trees and Shrubs Hardy in the British Isles. It wasn’t until the 1990s that horticultural trends started to lean seriously back towards the exotic, with new introductions from Edward Needham pioneering the fashion for hardy architectural plants, particularly Araliaceae, in temperate climates, and Christopher Lloyd courting scandal by ripping out his old rose garden at Great Dixter and replacing it with an exotic garden to conjure ‘visions of the bizarre’ (Pavord 2014; Lloyd 2007; Hudson 2013). Tetrapanax papyrifer suited this new aesthetic perfectly; it is prized for its architectural qualities and dramatic foliage, with large sprays of fluffy cream pompom-like flowers which appear late in the season and are attractive to pollinators (Machado, Giannotti & Olivieri 1988). It gained an Award of Garden Merit from the RHS in 1993, and has maintained a firm fanbase amongst gardeners looking for tropical jungle effects in temperate climates – even Facebook has a dedicated ‘Tetrapanax Growers UK’ page administered by expert grower Steve Jacobs, former manager of Mulu Nurseries.
Although frost can damage the growing tip and cause plants to be deciduous, or perhaps relegated to the status of a gigantic herbaceous perennial in colder climates, Tetrapanax papyrifer is root-hardy once established, and has been observed to re-grow from suckers at the base (or lower down the stem) when cut back by air temperatures of –8° to –12°C. The species is reportedly variable in hardiness and habit, and this may be due to early seed collections being sourced from relatively low elevations, although such details are not well documented. In 2024, a survey of plant records from 154 collections showed Tetrapanax papyrifer to be cultivated successfully outside without winter protection in gardens in Germany and Belgium, and across the UK including Scotland, northern England, the Midlands and East Anglia, although it was more commonly cultivated in collections from the warmer south-east and milder south-west of England (Collings 2024). It is commonly reported in the southern United States and as an escapee in Florida (GBIF 2024; Perdue & Kraebel 1961; Dave’s Garden 2021). It is recommended that young plants are given some winter protection until the stem has developed woody growth, and in colder regions it is wise to plant it in a sheltered spot, which also prevents the foliage becoming tattered by wind.
The suckering habit of Tetrapanax papyrifer has led to fears of it becoming invasive, particularly in warmer climates. Doug Smith, curator of the National Collection of Araliaceae in Hampshire, UK, reports suckers pushing up through patio slabs, and plants at the Sir Harold Hillier Gardens have been observed suckering at least 6 m from the parent plant (pers. obs.). Bamboo barriers may be helpful, or planting in a lawn where the suckers can be regularly mowed; it would be unwise to plant it outside a garden environment. Although it prefers a moist, well-drained rich soil, it tolerates a wide range of soils types; at Walmer Castle in Kent, Head Gardener Philip Oostenbrink grows six clones in a dry moat, on very well drained chalk and shingle, so successfully that they are applying for National Plant Collection status in 2025 (P. Oostenbrink, pers. comm.). However, it is commonly reported that winter wet and waterlogging may cause more damage than frost in British gardens.
Pests and diseases are rarely reported, although anthracnose and various leaf spot diseases have been observed for the first time in China, and Tortrix moth can occasionally be a problem (Tang et al. 2023; Wu et al. 2023; Jacobs 2022). It can be grown in full sun, but as a woodlander by nature it prefers some shade, especially when young, which will also have the effect of creating larger leaves; in full shade the plant may become straggly. Propagation is most easily carried out by splitting suckers from parent plants, or by root cuttings in March. It rarely sets seed in the UK: Steve Jacobs reports only 3 out of 1700 members of Tetrapanax Growers UK had seed after a mild autumn (pers. comm. 2025). Seed has a short viability of approximately 2 months, and should be surface-sown as fresh as possible (S. Jacobs pers. comm. 2025). Tissue culture of cultivars is becoming more common in commercial production: in 2025 Kevin Hobbs of Pinnacle Plants International reports they have 5000 tissue culture plants in production for general garden centre sales, which would have been unheard of several years ago.
Recent introductions of typically high elevation provenances have greatly diversified the cultivated population, and have no doubt helped to further popularise Tetrapanax papyrifer. In the wild the leaves are observed to become larger as elevation increases, whilst colonies become smaller (Avent 2008), leading to new introductions of larger-growing, hardier plants less prone to suckering. Cultivars named in recent years benefit from some combination of these characteristics, but so far as we have been able to deduce none of the known cultivar names represents a single genotype. Rather, cultivar names have been applied to groups of sister seedlings, therefore in this genus cultivar names denotes a particular provenance or race, but plants grown under the same cultivar name will exhibit some variation. The only sensible course of action in these circumstances is to treat all the cultivars as horticultural Groups (see below).
As new collections increase the genetic diversity of the cultivated population, along with a warming climate, Tetrapanax papyrifer looks set to remain a favourite amongst gardeners with a penchant for architectural foliage plants and gardens large enough to accommodate it. Growers are reminded, however, that Tetrapanax is known to cause unpleasant reactions with human skin, eyes and lungs due to its dense irritant hairs (M. Clifford & J. Grimshaw, pers. comms. 2025).
A Crûg Farm selection made at altitude on Dasyueshan in north west Taiwan in 2007 (BWJ 12488) (Crûg Farm 2025). At up to 5 m tall with leaves to over 1 m across with ginger indumentum, it is among the largest and most striking of selections. At Walmer Castle (Kent, UK) it is reported to be fast-growing and to sucker profusely (P. Oostenbrink pers. comm.). It is named for Diane Doughty and Sue Wynn Jones of Crûg Farm, and plays to the name of the mountain where seed was collected.
Large plants up to 5 m tall and with leaves over 1 m across, with deeply incised lobes, aristate lobe apices, and ginger indumentum. Collected in 1999 by Bleddyn and Sue Wynn Jones (BSWJ 7135) from a higher altitude than their previous collection of 1993, and perhaps more frost hardy than plants grown under any permutation of the name ‘Rex’ (Crûg Farm 2025). Philip Oostenbrink, Head Gardener at Walmer Castle (Kent, UK) observes more serration on the leaf margins and less indumentum than in typical forms. Its major advantage in the garden, that it doesn’t sucker, is also its undoing, making it very difficult to propagate. Subsequent seed collections have failed, whilst root cuttings have also been unsuccessful, with the effect of also killing several mother plants (Crûg Farm 2025). At the time of writing it is not available in the nursery trade.
A collection (NMWJ 14580) gathered with Taiwan’s Natural Science Museum under strict agreement that permission must be sought to propagate commercially under the rules of the CBD, material has been shared privately among a few UK gardens. Seed was collected from a colony of particularly large specimens, up to 10 m tall, from a high-altitude forested area known as Meifeng, an exposed area which is cold and icy during the winter. Fast growing with massive foliage up to 1.5 m across, emerging covered in a gingery indumentum (Crûg Farm 2023).
RHS Hardiness Rating: H4
Variable in form, but overall larger plants than typical for the species, occasionally up to 4 m tall, with leaves over a metre wide, which have dense, pale beige indumentum on new growth and the undersides of the leaves. The palmate lobes may be narrower and more deeply incised, perhaps with a more aristate instead of acuminate apex (pers. obs.). It is considered hardier and only suckers occasionally in undisturbed ground (digging around the roots will encourage suckering, a successful method of propagation previously used at Mulu Nurseries (M. Jacobs, pers. comm. 2025)).
There is enough confusion surrounding the identifying features of plants labelled ‘Rex’ (or any permutation of that name) to keep growers in constant debate and, sadly, for the name to have very little meaning anymore. The Editors of Trees and Shrubs Online consider treating this and all other cultivars as horticultural Groups to be the only sensible course of action.
The particular confusion surrounding the Rex Group is probably due to the convoluted nature of its introduction, of which details vary, but to the best of our understanding is as follows. Bleddyn and Sue Wynn-Jones of Crûg Farm Plants collected the seed in 1993 from a river bank in northern Taiwan, under the collector code BSWJ 1925; the plants were chosen for their dense, pale fawn to beige indumentum (B. Wynn-Jones, pers. comm. 2025). Tetrapanax papyrifer is fairly uniform from seed, which is why Crûg Farm have since introduced several first generation seed generated named plants, all from distinct isolated colonies at high altitudes (B. Wynn-Jones, pers. comm. 2025). Once back in the UK, unbeknownst to Crûg Farm, the seed was distributed erroneously as Aralia decaisneana, under a different collector code, to Pine Lodge in Cornwall, Powys Castle in Wales, and to the late Maurice Mason in Norfolk, amongst others. Plants believed to be grown from this seed collection arrived at Mulu Nurseries in 2001 from Powys Castle as part of a plant exchange (S. Jacobs, pers. comm. 2025). Whilst visiting Mulu Nurseries, plantsman Paul Spracklin, who had previously seen similar plants in Cornwall and observed jokingly that they should be called ‘Rex’, as the king of the Tetrapanax, mentioned this name, and it was subsequently listed in the catalogue as such (P. Spracklin, pers. comm. 2025). This is often referred to as the “Mulu Rex” form, whilst plants reportedly grown from the original seed collection in Cornish gardens are sometimes referred to as “Cornish Rex”, and are observed to have more deeply lobed or forked lobes, and a dark red petiole and veining in winter, as well as being considered less hardy. Crûg Farm retrospectively listed their collection BSWJ 1925 as ‘Rex’. With the popularity of ‘Rex’ increasing, a batch of tissue culture plants arrived on the market labelled “Tetrapanax papyrifera”, the incorrect spelling of the specific epithet said by Tetrapanax aficionados to be a useful means of spotting a “false Rex”. These plants appear to be no different to typical forms of T. papyrifer.
USDA Hardiness Zone: 7-6
Introduced by Cistus Nursery of Portland, Oregon in 1997, and named for being larger in all its parts and faster-growing than the rounder-leaved plant extant in North American gardens at the time; it appears to achieve greater size in warmer areas of North America (zone 8b south) than in Britain (reportedly up to 6 m tall in North America compared to 2–3 m in Britain), with leaves 1–1.8 m wide and lobes more deeply incised, having ginger indumentum on emergence which changes to light green on the mature leaf (S. Jacobs, pers. comm. 2025; Cistus Nursery 2021). According to Sean Hogan (pers. comm. 2025) it has proven to be hardier than typical forms of the species (up to 6°C more frost hardy; USDA zone 6–7), less suckering but more deciduous in habit. At Walmer Castle in Kent, UK, Philip Oostenbrink has observed that it differs in its shorter petioles and ‘stumpier’ habit (pers. comm. 2025).
The original provenance of this plant is unknown. It was taken from Japan to Hawaii during a relocation and subsequently to the San Francisco Bay area where it was given to the nurseryman Ed Carmen of Carmen’s Nursery. It was kept containerised for many years, during which time it was spotted by plantsman Roger Warner, who was excited to see what appeared to be a dwarf Tetrapanax. Ed eventually gifted the plant to Roger, and it was planted as an intended ground cover under a grove of Trachycarpus wagnerianus. Released from the confines of its pot, the Tetrapanax outgrew the Trachycarpus within a couple of seasons, and seeing its potential, Roger shared it with Cistus Nursery, where it was named ‘Steroidal Giant’ (S. Hogan, pers. comm. 2025).
Steve Jacobs had a stable variegated form, tentatively named ‘Variegata’ but Latinate cultivar names are only permissible if published before 1959; any published after this date are automatically invalid and those plants should be renamed. Root cuttings of this plant have only yielded one other variegated pup that fell foul of slugs, and an opportunity for tissue culture propagation was refused because it would lead to the death of the mother plant. In his experience of producing thousands of root cuttings, Steve says variegated forms are really a one-off: there are none available at the time of writing (S. Jacobs pers. comm. 2025).