Subfamily Aroideae·Tribe Aglaonemateae

Aglaonema

Aglaonema[ˌæɡloʊˈniːmə]
From the Greek aglaós (ἀγλαός) — shining and nêma (νῆμα) — thread, for the stamens; Schott named it in 1829
ARACEAE · THE GENUS

DESCRIPTION

Aglaonema is a genus of 26 accepted species of evergreen herbs in the family Araceae, native from northeastern India and Bangladesh through Myanmar, Indo-China and southern China, down the Malay Peninsula and across the Malay Archipelago to the Philippines, Sulawesi, the Moluccas and New Guinea. Nicolson, who revised the genus in 1969, called them relatively inconspicuous plants of dark places in the rain forest of southeastern Asia. Most stand on an erect, scarcely branched stem that sheds its lower leaves as it grows, so that the leaves crowd at the top of a stem ringed below with leaf scars; the few creeping species have stems that lie under the humus, buried there by fallen leaves. The leaves are often patterned in silver and pale green. The genus belongs to the tribe Aglaonemateae of the subfamily Aroideae, which it shares with Aglaodorum, a plant of tidal mudflats, and Boycea, a Bornean genus named in 2022. Its flowers are unisexual and naked: at the foot of the spadix a short zone of pistils, each a one-chambered ovary holding a single ovule, and above them free stamens, tightly packed, with no perianth and no consistent grouping to mark out a flower, so that Nicolson found it almost impossible to say how many make one. The fruit is a berry that turns from green through yellow, rarely white, to red, around a single seed almost as large as itself, with no endosperm. The name means “shining stamen” in Greek. Schott published it on September 8th, 1829, in the Viennese Wiener Zeitschrift für Kunst, founding it on a plant grown at Schönbrunn that he called Aglaonema oblongifolium; in 1832 he renamed it Aglaonema integrifolium and described it as perhaps an Indian plant, with a whitish, sweet-scented spathe. Both names, Nicolson showed, belong to the Penang species that Jack had described in 1820 as Calla nitida, and Aglaonema nitidum is the type of the genus.

The plant on the windowsill is the Chinese evergreen: in the United States, Nicolson wrote, Aglaonema modestum was commonly called so and was popular as a house plant; in Chinese it is “Wan-lien-tching,” literally “10,000 years green,” and is thought to bring good fortune to its owner. The species was long thought to be native to the Philippines, where its type was supposedly collected, but Merrill thought it highly probable that the type had been gathered in Manila from plants the Chinese had brought from southeastern China, a species they had probably cultivated for a long time and spread through the Orient, as more recently in the United States; Nicolson’s findings supported him. Gardens have been part of the genus from the start: by the time Kunth gathered it together in 1841, several species were in cultivation as ornamental foliage plants, and N. E. Brown described six new species from cultivated plants in the late 1880s and early 1890s, among them Aglaonema rotundum, whose “native country” he did not know. The cultivars, in Henny’s 1988 account, came from wild-collected species and from mutations noticed by collectors and nurserymen; breeding played a small part, though four important commercial cultivars were hybrids raised in Florida in the 1960s.

sect. Aglaonema stem erect, rarely decumbent or branching; petiole sheath usually more than 1 cm long; cataphylls usually only below the inflorescences; most species, Aglaonema nitidum, the type of the genus, among them
sect. Chamaecaulon stem creeping, often branching; petiole sheath under 1 cm, less than a fifth of the petiole; a cataphyll clasping each petiole; Aglaonema costatum (the type) and Aglaonema brevispathum, with Aglaonema chermsiriwattanae, reported to lack the cataphylls, in the Flora of Thailand

Nicolson recognized the two sections for the first time in 1969, naming Chamaecaulon as new. In its creeping stems, very short sheaths and cataphylls among the leaves he found it similar to Aglaodorum and the African Anubias, both plants of tidal mudflats or swamps, and he saw the small, poorly known Aglaonema pumilum and Aglaonema rotundum as intermediate between the two sections. He once thought of a third section for the three northern species with a sessile spadix, Aglaonema ovatum, Aglaonema modestum and Aglaonema hookerianum, and gave it up, since nothing else set them apart and subsessile spadices turn up in other species too. In 2020 Van and colleagues, sequencing chloroplast DNA from plants of southern Vietnam, found Aglaodorum griffithii nested within Aglaonema and proposed to sink Aglaodorum into it; Kew still keeps Aglaodorum as a genus of one species.

Aglaodorum pistils in a single whorl (as also in Aglaonema flemingianum); a long peduncle, about as long as the petiole; spongy stems and petioles; ripe fruits green, spongy and floating; tidal mudflats
Homalomena aromatic tissues; a staminode beside each pistil; ovary of several incomplete chambers with many ovules
Schismatoglottis upper spathe and spadix deciduous; a sterile tip to the male zone; ovary with many ovules
Dieffenbachia American; stamens fused into synandria; four staminodes below each pistil; ovary of two or three chambers

The Flora of Thailand finds the genus readily identified by its suffruticose habit and distinctive infructescences; leaves alone are another matter, for some species of Dieffenbachia, Nicolson wrote, cannot be told from Aglaonema with certainty from vegetative material, and Schismatoglottis, occasionally confused with it, is easily told by its inflorescence. The creeping species look superficially like some Homalomena but lack its aromatic tissues and bear their red berries exposed. Schott and Engler separated Aglaodorum by staminodes among its pistils, which Nicolson took for a misreading of a pressed fruiting specimen; the Flora of Thailand, finding them hard to see, tells it more readily by its spongy rhizome and petioles and its large spongy fruits, which float away when ripe, where the fruits of Aglaonema are red, or more rarely pink, and dispersed by birds.

Chinese evergreen English, United States · Aglaonema modestum; the genus
Wan-lien-tching Chinese, “10,000 years green” · Aglaonema modestum
Guang dong wan nian qing shu Chinese · the genus
Guang dong wan nian qing Chinese · Aglaonema modestum
Yue nan wan nian qing Chinese · Aglaonema simplex
Khiao muen pi Thai · Aglaonema modestum
Bai sam si, sam si, ai bai sam si Thai · Aglaonema costatum
Kap choeng thian Thai, Peninsular · Aglaonema chermsiriwattanae
Kluai tao, hua laman Thai, Southwestern · Aglaonema cochinchinense
Hora Thai, Trat and Peninsular · Aglaonema brevispathum, Aglaonema nitidum, Aglaonema simplex
Cha ngot khao Thai, Peninsular · Aglaonema nitidum
Ratsami ngoen, rio ngoen Thai · Aglaonema nitidum
Wan khan mak Thai, Central · Aglaonema simplex
Lempoei, lempoeng Sundanese, Bogor · Aglaonema simplex
Gavay sin buaya, panan quilon Leyte and “Omauvana,” 1704 · Aglaonema commutatum or Aglaonema robeleynii

Chinese evergreen is the name Nicolson found in use for Aglaonema modestum in the United States, and the Genera of Araceae gives it to the genus. Besides Nicolson’s Wan-lien-tching, the Chinese names are those of the Flora of China, which builds the names of the genus and of both its Chinese species on wan nian qing; the Thai names are those of the Flora of Thailand. Lempoei, with its probable variant lempoeng, is the only local name Nicolson found recorded more than twice for Aglaonema simplex, on three plants cultivated at Bogor, though he thought it might be more an adjective, for light or soft wood, than a name. The earliest in print are Kamel’s, the first author, Nicolson says, to publish on a species of the genus: in 1704 Kamel recorded that his “Dracunculus Luzonis primus,” a plant with white-spotted leaves from Leyte and “Omauvana,” was called gavay sin buaya and panan quilon. Nicolson could not decide whether it is Aglaonema commutatum or the plant he called Aglaonema crispum, now Aglaonema robeleynii; Kew places Blume’s name for it, Aglaonema maculatum, under Aglaonema commutatum.

ARACEAE · RANGE

DISTRIBUTION

Wholly Asian, in the tropics and subtropics. Kew maps the genus in 20 places, from Assam, the eastern Himalaya and Bangladesh through Myanmar, Thailand and Indo-China to southern China, out to the Nicobar Islands, down the Malay Peninsula to Sumatra, Java, Borneo and the Lesser Sunda Islands, and east through the Philippines and Sulawesi to the Moluccas and New Guinea. One species covers most of it. Aglaonema simplex is native in 16 of the 20 places, and Nicolson called it the most variable species in the genus, tending at the edges of its range to intergrade with others: in Myanmar and western Thailand, where the northern species with sessile spadices may be its closest relatives, and in the Philippines and Sulawesi, where it may contribute, with Aglaonema nitidum and Aglaonema marantifolium, to the variability of the plants there. Blume described Aglaonema simplex and Aglaonema marantifolium together in 1837, and to Nicolson the first was one of the commonest species of western Malesia and the second the commonest of eastern Malesia; Aglaonema marantifolium, of the Moluccas and New Guinea, is the only species Kew records in New Guinea.

On Kew’s count Malesia holds 16 of the 26 species, Indo-China 12, the Indian subcontinent 8, China 2 and Papuasia 1. Thailand has the most, 9, the same nine the Flora of Thailand describes; Myanmar, Vietnam and the Philippines have 7 each. Eleven species are native to a single place: Aglaonema chermsiriwattanae in Thailand, Aglaonema flemingianum in Peninsular Malaysia, Aglaonema manabendrae in Assam, Aglaonema tassae in the eastern Himalaya, Aglaonema nicobaricum in the Nicobars, Aglaonema cordifolium, Aglaonema robeleynii and Aglaonema tricolor in the Philippines, and Aglaonema pictum, Aglaonema rotundum and Aglaonema vittatum in Sumatra. Engler recognized 41 species in 1915; Nicolson, counting 76 binomials published in the genus, accepted 21 in 1969. Kew’s 26 fold his Aglaonema tenuipes into Aglaonema simplex and reduce his Aglaonema stenophyllum to a variety of Aglaonema philippinense, but restore Aglaonema birmanicum and Aglaonema nicobaricum, which he had sunk in Aglaonema simplex and which the Flora of Thailand still sinks there, as the Flora of China does Aglaonema birmanicum; and they add five species named since, Aglaonema tricolor in 1980, Aglaonema chermsiriwattanae in 1997, Aglaonema flemingianum in 1998, Aglaonema tassae in 2018 and Aglaonema manabendrae in 2021. Kew lists species of the genus as introduced in ten places, nine of them for Aglaonema commutatum, from India and Bangladesh to the Comoros, the Cook Islands and the Caribbean; its ability to naturalize, Nicolson found, makes it hard to be certain which collections from its native Philippines and Sulawesi come from the wild and which are escapes.

Borneo · Java · Lesser Sunda Islands · Maluku · Peninsular Malaysia · Philippines · Sulawesi · Sumatra
Cambodia · Laos · Myanmar · Nicobar · Thailand · Vietnam
Assam · Bangladesh · East Himalaya
China South-Central · China Southeast
New Guinea
ARACEAE · CYTOLOGY

CHROMOSOMES

CHROMOSOME NUMBER (2n)

2n = 40 in 6 of the 10 species counted (60%).

2n = 406 species · 60%
2n = 142 species · 20%
2n = 422 species · 20%
2n = 602 species · 20%
+ 12 rarer counts
2n = 101 species · 10%
2n = 131 species · 10%
2n = 161 species · 10%
2n = 221 species · 10%
2n = 271 species · 10%
2n = 381 species · 10%
2n = 561 species · 10%
2n = 801 species · 10%
2n = 1001 species · 10%
2n = 1181 species · 10%
2n = 1191 species · 10%
2n = 1201 species · 10%

Shares add up to more than 100% because some species have been counted at more than one number, usually diploid and polyploid forms of the same species (e.g. Aglaonema brevispathum at 10 and 13 and 27 and 38 and 40).

COUNTS

10 of 26 species have a published 2n count.

Base chromosome number: x = 6 (Henny et al. 2009; Nicolson 1969), x = 20 (Nicolson 1969).

What chromosome numbers mean for a cross, in the Chromosomes and Crossing guide.

Counted species (10)
  • Aglaonema brevispathum10, 13, 27, 38, 40
  • Aglaonema cochinchinense40
  • Aglaonema commutatum14, 118, 119, 120
  • Aglaonema costatum14, 22, 40
  • Aglaonema modestum56
  • Aglaonema nitidum40
  • Aglaonema pictum16, 40, 42
  • Aglaonema robeleynii60
  • Aglaonema simplex40, 42, 60
  • Aglaonema treubii80, 100
Sources (8)
  1. Chen, J.; Devanand, P. S.; Norman, D. J.; Henny, R. J.; Chao, C. T. 2004. Genetic Relationships of Aglaonema Species and Cultivars Inferred from AFLP Markers. Annals of Botany 93(2): 157–166.
  2. Henny, R. J.; Chen, J. 2003. Cultivar Development of Ornamental Foliage Plants. Plant Breeding Reviews, Volume 23 (ed. J. Janick), John Wiley & Sons 23: 245.
  3. Henny, R. J.; Chen, J.; Mellich, T. A. 2009. Tropical Foliage Plant Development: Breeding Techniques for Aglaonema and Dieffenbachia. EDIS (University of Florida IFAS Extension) 2009(5).
  4. Marchant, C. J. 1971. Chromosome variation in Araceae: II. Richardieae to Colocasieae. Kew Bulletin 25(1): 47–56.
  5. Nicolson, D. H. 1969. A Revision of the Genus Aglaonema (Araceae). Smithsonian Contributions to Botany 1.
  6. Sharma, A. K.; Datta, K. B. 1961. A Cytological Study to work out the Trend of Evolution in Aglaonema and Richardia. Caryologia 14(3): 439–454.
  7. Subramanian, D.; Munian, M. 1988. Cytotaxonomical Studies in South Indian Araceae. Cytologia 53(1): 59–66.
  8. Yeh, D. M.; Yang, W. J.; Chang, F. C.; Chung, M. C.; Chen, W. L.; Huang, H. W. 2007. Breeding and Micropropagation of Aglaonema. Acta Horticulturae 755(755): 93–98.
ARACEAE · IN THE WILD

ECOLOGY

CLIMATE

Aglaonema is a genus of humid tropical forest, in the words of the Genera of Araceae, and only occasionally of deciduous forest or regrowth; Boyce and colleagues give primary and secondary perhumid to everwet evergreen forest, with a few species restricted to kerangas or to monsoonal semi-deciduous forest, the last not in Borneo. Aglaonema simplex rarely grows above 1,500 m, though it has been reported at “7000 feet” on Mount Kinabalu, and Aglaonema hookerianum keeps below 1,000 m, in forest that receives more than 80 inches of rain a year. Aglaonema pictum is usually recorded between 1,000 and 2,000 m on the slopes of the major volcanoes of Sumatra, and Aglaonema nebulosum, a plant of lowland swamp forest in Nicolson’s account, was reported by Singh and colleagues in 2018 from 1,100–1,600 m in the wet hill forest of Meghalaya, its first record in India. Aglaonema nitidum, Nicolson found, flowers without season, being largely restricted to the equatorial region, where rain falls daily rather than seasonally and the plants live in dark places where the humidity is always high. Where the year has a wet season, Nicolson tied flowering to it: Aglaonema ovatum flowers in April and May and Aglaonema hookerianum in June and July, both probably in response to the onset of the summer monsoon. In Thailand the Flora finds the genus most abundant in the wetter south and north, though the species with rhizome-like stems tend to keep to seasonally dry mixed deciduous and evergreen forest. The charts below draw the genus’s measured envelope across its native range, and all 20 of its native places resolve in the climate data.

HABITAT

The species are terrestrial herbs of the tropical forest floor, almost always in shade, as Van and colleagues put it. The larger plants lean: Aglaonema marantifolium rarely stands erect over five feet, Nicolson observed, although its stem may be up to ten feet long, and Aglaonema rotundum seems to pull its stem down with contractile roots. Some grow on limestone or in peat: Aglaonema costatum in damp, shady places at the foot of limestone hills on Langkawi, Aglaonema nitidum in lowland dipterocarp forest, freshwater peat-swamp forest and damp pockets on limestone, and Aglaonema nebulosum in peat and freshwater forests in Nicolson’s account, though Boyce and colleagues describe it as restricted to kerangas. A species can be dense: in a 16-hectare plot of dry evergreen forest at Sakaerat in northeastern Thailand, O-Thong and colleagues counted 11,232 plants of Aglaonema simplex, 702 to the hectare, growing in clumps. At Mulu in Sarawak, Chai and Wong found that anthesis in Aglaonema nitidum and Aglaonema simplex lasts 26 hours: the female flowers become receptive at about four in the morning, as the spathe opens wide and the male zone gives off a scent reminiscent of citrus alcohol, and the pollen is shed the next morning. Flies of the genus Colocasiomyia, in their view the most likely pollinators, feed on the stigmatic secretions and pollen and mate on the male zone; the flies of the Colocasiomyia toshiokai group are recorded only on Homalomena and Aglaonema, and in the botanic garden at Bogor Colocasiomyia heterodonta laid its eggs on a spadix of Aglaonema pictum. At Mulu the fruits took about three months to ripen. The Flora of Thailand has them dispersed by birds, but O-Thong and colleagues, citing earlier reports, note that the ripe fruits of Aglaonema simplex tend to fall and germinate beside the parent, and take this to explain its clumps; in Bali, Lestari and Asih found its seeds broken by a bird and suspected that birds spread them too, though not far.

Araceae · Form

Morphology

A herb of the forest floor, usually a cane-like stem crowned with leaves that are often patterned in silver, in a few species a stem that creeps beneath the leaf litter. The flowers are naked and single-sexed, and each female flower is a single chamber with a single ovule, which ripens into a berry, red in most species, holding one large seed with no endosperm.

A short, cane-like stem that sheds its lower leaves and lies down when it grows too heavy, or, in a few species, a creeping stem buried by leaf fall. Every node holds a bud and can root, and in Aglaonema marantifolium a ring of canals full of gummy sap runs through the stem.

The stem

Most species of Aglaonema, in Nicolson’s 1969 revision, are erect, with relatively unbranched stems and distinct internodes. Growth is continuous but the lower leaves fall, leaving a tuft of leaves at the top of a stem marked below by circular leaf scars, an erect habit Nicolson found rather unusual in the family. Aglaonema vittatum stands 10–15 cm tall on a stem 2–7 mm thick, while Aglaonema densinervium, which Nicolson thought probably the largest species, reaches 90–200 cm on a stem up to 6 cm thick.

Tall stems do not stay upright. A stem of Aglaonema marantifolium may be ten feet (3 m) long, Nicolson wrote, but cannot carry the weight of the plant, and large plants recline against their neighbors without climbing. On a rocky mountaintop on Panay the collector B. Frank Brown reported in 1982 the pink-petioled aglaonema grown as ‘Tricolor’ by the thousands, its stems 6 to 8 feet (about 2–2.5 m) long twining around the cliffs, fallen over and still growing.

Creeping stems

In Aglaonema brevispathum and Aglaonema costatum, which Nicolson set apart as section Chamaecaulon, the stem is repent and branched, usually less than 1 cm thick, with internodes usually under 0.5 cm. In the wild it lies beneath the humus of the forest floor and looks subterranean, but leaf fall has only buried it, and in cultivation it creeps on the surface. Aglaonema pumilum and Aglaonema rotundum seemed to Nicolson to fall between the two sections, decumbent and sometimes with cataphylls among the leaves.

Buds, roots and sap

Erect plants look unbranched, but every node holds a reserve bud, which usually waits until the shoot tip is lost; Nicolson saw such buds grow out wherever a node was strongly rooted, which is why the creeping stems branch freely. Roots arise at the nodes, often nearly as thick as the stem in section Chamaecaulon, up to 0.5 cm in Aglaonema costatum, and the Flora of Thailand found the decumbent stems of larger Aglaonema ovatum producing greatly thickened roots, a feature not reported before and apparently diagnostic. Inside the stem of Aglaonema marantifolium, Van Tieghem found in 1867 a ring of about 20 schizogenous canals, each about 0.24 mm across and full of gummy sap; the stem of Aglaonema simplex was almost the same but lacked them.

01Erect, cane-like stems ringed with leaf scars, from 10–15 cm in Aglaonema vittatum to 2 m in Aglaonema densinervium; decumbent once too heavy, not climbing in the usual sense.
02Creeping, branched stems buried by leaf fall in section Chamaecaulon (Aglaonema brevispathum, Aglaonema costatum); Aglaonema pumilum and Aglaonema rotundum in between.
03A reserve bud at every node, growing out when the node is well rooted or the shoot tip is lost.
04Roots from the nodes, greatly thickened in Aglaonema ovatum; a ring of gummy canals in Aglaonema marantifolium, none in Aglaonema simplex.
Four images. A photograph of an Aglaonema simplex plant on a dark forest floor of leaf litter, a single upright stem crowned with a tuft of narrow leaves on long stalks; a line drawing in outline of the flowering stem of Aglaonema commutatum, the bases of the leaves wrapped around the stem, slender stalks of inflorescences rising among them, with typed labels for the leaf bases, the cataphylls, the peduncles and an axillary bud; a hand-colored lithograph of Aglaonema simplex showing a thick green stem ringed by the scars of old leaf bases beside a paler, uncolored plant whose stem curves down and lies along the ground, rooting all along its length; and a photograph of a lifted stem of Aglaonema tassae lying across a leaf, a short brown stem with many long, branching roots.

Fig · A short stem, erect or lying down

Araceae · In cultivation

Cultivation

UF/IFAS Extension calls the genus Chinese evergreen and counts it among the most popular tropical foliage plants, for its patterned leaves, its tolerance of low light and low humidity, and its few pests. Florida has grown it commercially since the 1930s, though it took almost 30 years for its ability to survive dim interiors to be widely recognized. The trade grows hybrids and selections for their leaves, and the growing guides advise removing the flowers.

Peat-based, moist and open, with a tenth to a fifth of its volume in air. The wild plants root in forest humus, limestone pockets and peat, and the danger the growing guides name is a pot that stays wet.

In the forest the plants root in humus. Mayo, Bogner and Boyce record them on the forest floor and in humus deposits on limestone and in peat, and Nicolson records Aglaonema nitidum from freshwater peat-swamp forest and from damp pockets on limestone. At Sakaerat in northeastern Thailand, O-Thong and colleagues found Aglaonema simplex commoner where the soil held more clay, had a higher pH and more exchangeable magnesium, and scarcer among rocky outcrops.

Florida’s production guidelines ask for a mix of sphagnum peat, pine bark, vermiculite or perlite with a total porosity of 50–75%, 10–20% of the volume as air, a dry bulk density of 0.2–0.8 g/cm³ and a pH of 6.0–6.5, kept moist at 50–80% of container capacity. In trials at Apopka begun in 1972, Conover and Poole grew ‘Fransher’ best in Peace River peat with cypress shavings, or with pine bark and sand, and worst in Douglas fir bark, sphagnum peat and perlite. The plant is not fussy: Gilman’s UF/IFAS profile finds any fertile, nematode-free soil or artificial mix suitable, and the plants survive in peat and perlite, in sand or in hydroponics. What they will not take is water that does not drain: NC State Extension asks for an acid, well-drained mix and ties root rot to overwatering, and the RHS, potting on every two or three years, warns of stem and root rots in very wet compost.

Aglaonema Timeline

An interactive timeline showing the year each Aglaonema species was first described as Aglaonema (species may previously have been classified in other genera)

Sources

The papers behind the morphology & cultivation tab

  1. Nicolson, D. H. (1969). A revision of the genus Aglaonema (Araceae). Smithsonian Contributions to Botany 1: 1–69.
  2. Mayo, S. J., Bogner, J. & Boyce, P. C. (1997). The Genera of Araceae. Kew: Royal Botanic Gardens. xii + 370 pp.
  3. Boyce, P. C., Sookchaloem, D., Hetterscheid, W. L. A., Gusman, G., Jacobsen, N., Idei, T. & Nguyen, V. D. (2012). Araceae. In: Santisuk, T. & Larsen, K. (eds), Flora of Thailand 11(2): 101–325. Bangkok: The Forest Herbarium.