1. Family: Orchidaceae Juss.
    1. Phalaenopsis Blume

      1. This genus is accepted, and its native range is Tropical & Subtropical Asia to NE. Australia.

    [A-EM]
    Distribution

    There are 45–50 species of Phalaenopsis collectively distributed from India (including Andaman and Nicobar Islands) to southern China, Korea, Japan, Thailand, Indochina, Malaysia, and Indonesia to the Philippines, Australia, and New Guinea. The majority of species occur in Indonesia and the Philippines.

    Ecology

    Phalaenopsis species are mainly epiphytes at 0–2500 m and occur primarily in three distinct habitats: seasonally dry areas, seasonally cool areas, and constantly warm and humid areas. The plants show adaptations to each of these (Christenson 2001). Species confined to monsoonal areas with a pronounced wet-and-dry cycle have adapted to the stress of the dry season in several ways. These include increased succulence in species such as P. cornu-cervi, in which the roots and leaves are thicker than other species of similar size. There are even unsubstantiated reports that P. cornu-cervi may be semi-deciduous in part of its range. Christenson (2001), however, pointed out that this may not be a direct adaptation to seasonal dryness because the sister species P. pantherina Rchb.f. is recorded from high in the forest canopy, where it is exposed to bright, diffuse light unlike most other species in Borneo that occur toward the base of trees under low-light conditions. Increased succulence in P. cornu-cervi may simply be a response to degree of exposure independent of seasonal dryness. The most extreme form of adaptation in Phalaenopsis native to seasonally dry areas is a deciduous habit, which eliminates excessive transpiration. This is seen primarily in several mainly Himalayan groups of Phalaenopsis, including P. sections Aphyllae and Parishianae. Species adapted to seasonally cool to cold conditions also occur in regions that are seasonally dry. It is difficult to say which adaptation came first because many adaptations apply to both extremes equally. The only truly cool- or cold-growing species belong to P. section Aphyllae. Phalaenopsis taenialis has been recorded as high as 2500 m in China and the Himalayan region, an elevation more typical of cold-growing genera. All these cold-growing species of Phalaenopsis are either deciduous or semi-deciduous in habit, accompanied by a strong dormancy, which affords some protection from cold damage. The majority of species in the genus, belonging to P. subgenus Phalaenopsis occur in areas that are uniformly warm and humid throughout the year. Most species occur in evergreen forests without a significant dry season. Within these forests is a mosaic of habitats, and Phalaenopsis species occur in most of them (Christenson 2001). Some species, such as P. gigantea J.J.Sm. and P. pantherina, occur relatively high in the canopy where conditions are exposed. These have leathery leaves to prevent desiccation and will tolerate higher light levels than many. Other species, such as P. fuscata Rchb.f. and P. tetraspis Rchb.f., grow under extremely low light levels. Many others occur in riparian habitats, such as along streams and rivers, which provide constantly high humidity regardless of local fluctuations in rainfall. Phalaenopsis violacea H.Witte occurs in swamps where humidity levels are also high. Species such as P. lowii and P. sumatrana Korth. & Rchb.f. are able to grow either as epiphytes or opportunistically as lithophytes. Christenson (2001) suggested that ‘life on large boulders may provide the plants with a steadier moisture supply or may take advantage of the light gap often associated with rock outcroppings in otherwise continuous forest’. The three species of P. section Esmeralda (formerly placed in the genus Doritis) and some Australian populations of P. amabilis (L.) Blume subsp. rosenstromii (F.M.Bailey) Christenson are unusual in being obligate terrestrials or lithophytes. Christenson (2001) commented that ‘both appear to be derived conditions within the genus, and an epiphytic habit is accepted as the ancestral character for the genus as a whole. In the cases of P. buyssoniana Rchb.f., P. pulcherrima, and P. regnieriana Rchb.f., the terrestrial habit appears to be an adaptation, in part, to an extremely pronounced dry season. Direct access to the soil and accumulated leaf litter presumably provide supplemental water during the dry season. Life on the ground for these three species, which are native to more or less deciduous forests, also presumably provides some shade even when the forest canopy is leafless. These species also show perhaps the strongest tendency for the leaves to turn reddish purple under intense solar radiation or water stress, another defence under extreme conditions’.

    General Description

    (Plates 91-96; Fig. 672.1-672.4) Terrestrial, lithophytic, and epiphytic herbs. Roots terete or flattened. Stem leafy, concealed by overlapping persistent leaf-sheaths, rooting mostly at base. Leaves alternate, distichous, succulent, persistent or sometimes deciduous, oblong to broadly elliptic, sometimes marbled or suffused with purple or silver. Inflorescence axillary racemes or panicles, axillary, erect to pendent; peduncle terete; rachis terete or bilaterally compressed, rarely swollen relative to peduncle; floral bracts usually inconspicuous, persistent, succulent or papery. Flowers 1–30, resupinate, produced simultaneously or in succession, often long-lasting, sometimes fragrant, plain or variously spotted, marbled, or barred. Sepals and petals free, spreading, subsimilar to dimorphic, lateral sepals usually oblique and larger than dorsal sepal. Labellum trilobed, clawed, continuous with column foot or rarely hinged at base of a footless column (species formerly included in Hygrochilus), sometimes saccate-spurred or subsaccate, side lobes erect and subparallel, often callose, midlobe oblong-elliptic to obtrullate, rarely transverse, sometimes pubescent to villose, apex sometimes bearing a pair of tendril-like appendages (cirrhi), callus uni-, bi- or triseriate, longitudinal, rarely transverse; sac or spur, if present, without internal ornamentation. Column often subtended by a pair of fleshy, knee-like protrusions, without wings, usually with a column foot, usually dilated lateral to stigma; pollinia two or four, on a common spatulate stipe and viscidium; rostellum sometimes beaked. Ovary pedicel terete, shallowly six-sulcate.

    Morphology

    Schill and Pfeiffer (1977) reported on the pollen of P. amabilis, P. lueddemanniana Rchb.f., and Doritis pulcherrima (= P. pulcherrima). Tetrads were convex with a laevigate surface and a rounded sexine (calymmate in P. pulcherrima) 1–2 μm thick.

    [A-EM]
    Use

    Phalaenopsis is currently the most important and popular orchid genus in cultivation, with species of P. sections Phalaenopsis and Esmeralda being particularly valuable in breeding programmes for the houseplant and cut-flower trade. No uses have been reported apart from some former medicinal use of P. aphrodite Rchb.f. and P. schilleriana Rchb.f. in the Philippines (Lawler 1984).

    Images

    Distribution

    Native to:

    Andaman Is., Assam, Bangladesh, Bismarck Archipelago, Borneo, Cambodia, China South-Central, China Southeast, East Himalaya, Hainan, India, Japan, Jawa, Korea, Laos, Lesser Sunda Is., Malaya, Maluku, Myanmar, Nansei-shoto, Nepal, New Guinea, Nicobar Is., Philippines, Queensland, Sri Lanka, Sulawesi, Sumatera, Taiwan, Thailand, Tibet, Vietnam, West Himalaya

    Introduced into:

    Panamá

    Phalaenopsis Blume appears in other Kew resources:

    Date Reference Identified As Barcode Type Status
    Jul 5, 2002 Borneo 52557.000
    Borneo 53628.000
    61732.000
    Cribb, P. [s.n.], Malaysia 55865.000
    Lamb, A. [AL255/84], Sabah 72925.000
    s.coll. [s.n.] 78099.000

    First published in Bijdr. Fl. Ned. Ind.: 294 (1825)

    Accepted by

    • Chase, M.W., Cameron, K.M., Freudenstein, J.V., Pridgeon, A.M., Salazar, G., van den Berg, C. & Schuiteman, A. (2015). An updated classification of Orchidaceae Botanical Journal of the Linnean Society 117: 151-174.
    • Pridgeon, A.M., Cribb, P.J., Chase, M.C. & Rasmussen, F.N. (2014). Genera Orchidacearum 6: 1-544. Oxford University Press, New York, Oxford.
    • Wu, Z. & Hong, D. (eds.) (2009). Flora of China 25: 1-570. Missouri Botanical Garden Press, St. Louis.
    • Govaerts, R. (2003). World Checklist of Monocotyledons Database in ACCESS: 1-71827. The Board of Trustees of the Royal Botanic Gardens, Kew.

    Sources

    Aeridinae: e-monocot.org
    All Rights Reserved

    Herbarium Catalogue Specimens
    'The Herbarium Catalogue, Royal Botanic Gardens, Kew. Published on the Internet http://www.kew.org/herbcat [accessed on Day Month Year]'. Please enter the date on which you consulted the system.

    Kew Backbone Distributions
    The International Plant Names Index and World Checklist of Selected Plant Families 2019. Published on the Internet at http://www.ipni.org and http://apps.kew.org/wcsp/
    © Copyright 2017 World Checklist of Selected Plant Families. http://creativecommons.org/licenses/by/3.0

    Kew Names and Taxonomic Backbone
    The International Plant Names Index and World Checklist of Selected Plant Families 2019. Published on the Internet at http://www.ipni.org and http://apps.kew.org/wcsp/
    © Copyright 2017 International Plant Names Index and World Checklist of Selected Plant Families. http://creativecommons.org/licenses/by/3.0