Bulbophyllum Explained

Bulbophyllum is a genus of mostly epiphytic and lithophytic orchids in the family Orchidaceae. It is the largest genus in the orchid family and one of the largest genera of flowering plants with more than 2,000 species, exceeded in number only by Astragalus. These orchids are found in diverse habitats throughout most of the warmer parts of the world including Africa, southern Asia, Latin America, the West Indies, and various islands in the Indian and Pacific Oceans.[1] Orchids in this genus have thread-like or fibrous roots that creep over the surface of trees or rocks or hang from branches. The stem is divided into a rhizome and a pseudobulb, a feature that distinguished this genus from Dendrobium. There is usually only a single leaf at the top of the pseudobulb and from one to many flowers are arranged along an unbranched flowering stem that arises from the base of the pseudobulb. Several attempts have been made to separate Bulbophyllum into smaller genera, but most have not been accepted by the World Checklist of Selected Plant Families.

Description

Plants in the genus Bulbophyllum are epiphytic or lithophytic sympodial herbs with thread-like or fibrous roots that creep over the surface on which they grow. The stem consists of a rhizome and a pseudobulb, the latter with one or two usually fleshy or leathery leaves. The flowers are arranged on an unbranched raceme that emerges from the pseudobulb, usually from its base. The dorsal sepal is free from the lateral sepals which themselves may be free or fused to each other. The petals are also free from each other and smaller than the lateral sepals. The labellum is often fleshy, curved and hinged to the base of the column.[2] [3]

Distribution and habitat

The center of diversity of this genus is in the montane forests of Papua New Guinea (more than 600 species) which seems to be the evolutionary homeland,[4] though the genus is pantropical and widespread, occurring in Australia, Southeast Asia (with over 200 species in Borneo), India, Madagascar (with 135 species, some endemic), Africa and in tropical central and South America.

The erect to pendent inflorescence arises laterally from the base of the pseudobulb. The flower form has a basic structural blueprint that serves to identify this genus. But this form can be very diverse : compound or single, with few to many flowers, with the resupinate flowers arranged spirally or in two vertical ranks. The sepals and the petals can also be very varied : straight or turned down, without footstalk or with a long claw at the base. They are often hairy or callous. There are two to four hard and waxy pollinia with stipes present or absent. The fruits are beakless capsules.

Taxonomy and naming

The genus Bulbophyllum was first formally described in 1822 by Louis-Marie Aubert du Petit-Thouars in his book Histoire particulière des plantes orchidées recueillies sur les trois Iles Australes d'Afrique, de France, de Bourbon et de Madagascar in which he described eighteen species of Bulbophyllum.[5]

There are now more than 2,800 records (accepted names and synonyms) for this genus. This large number and the great variety of its forms make the genus a considerable challenge for taxonomists: 120 sections and subgenera have been listed.[6]

The genus name (Bulbophyllum) is derived from the Greek bolbos meaning 'bulb' and phyllon, 'a leaf', referring to the pseudobulbs on top of which the leaf grows.[7] [6]

In 2014, Alec Pridgeon and others proposed merging the genus Drymoda with Bulbophyllum in the Genera Orchidacearum and the change is accepted by Plants of the World Online and the World Checklist of Selected Plant Families.[8] [9] [10] The former species of Drymoda included D. digitata (now B. digitatum),[11] D. gymnopus (now B. gymnopus),[12] D. latisepala (now B. capillipes),[13] D. picta (the type species of Drymoda, now B. drymoda),[14] and D. siamensis (now B. ayuthayense).[15]

Evolution and biogeography

Molecular phylogenetic studies place the origin of the orchid genus Bulbophyllum into the early Miocene. Biogeographic analyses and ancestral area reconstructions identified the Asia-Pacific region as the ancestral area of Bulbophyllum and suggest an early-to-late Miocene scenario of 'out-of-Asia-Pacific' origin and progressive (east-to-west) dispersal-mediated diversification, resulting in three additional radiations in Madagascar, Africa and the Neotropics, respectively.[16]

Sections

In 2019 Bulbophyllum were separated into four clades Neotropics, Africa, Madagascar, and the Asia-Pacific.[17] [18]

Africa Clade

Image Section Type species
Bulbophyllum bifarium
Carnosisepala Bulbophyllum carnosisepalum
Chaseela Bulbophyllum pseudohydra
Comata Bulbophyllum comatum
DenticulataBulbophyllum denticulatum
GenyorchisBulbophyllum apetalum
GenyorchisBulbophyllum deshmukhii
GilgianaBulbophyllum gilgianum
Bulbophyllum falcatum
Bulbophyllum barbigerum
Bulbophyllum oreonastes

Madagascar Clade

Image Section Type species
Bulbophyllum occlusum
BifalculaBulbophyllum implexum
BulbophyllumBulbophyllum nutans
Bulbophyllum oxycalyx
Ikongoense Bulbophyllum ikongoense
InversifloraBulbophyllum cardiobulbum
KinethrixBulbophyllum mirificum
Bulbophyllum lichenophylax
Bulbophyllum occultum
LyperocephalumBulbophyllum lyperocephalum
Moratii Bulbophyllum moratii
PachychlamysBulbophyllum pachypus
PantoblepharonBulbophyllum pantoblepharon
PloiariumBulbophyllum coriophorum
PolyradicesBulbophyllum petrae

Neotropical Clade

Image Section Type species
Bulbophyllum bracteolatum
Bulbophyllum exaltatum
Bulbophyllum nagelii
Bulbophyllum micranthum
Bulbophyllum napellii
Bulbophyllum chloropterum

Asia-Pacific Clade

Image Section Type species
Bulbophyllum kingii
Bulbophyllum bracteatum
Bulbophyllum dryas
Bulbophyllum elongatum
AntennataBulbophyllum fuscopurpureum
Balaenoidea Bulbophyllum balaeniceps
Bulbophyllum beccarii
Bulbophyllum biflorum
Bulbophyllum bisetum
BlepharistesBulbophyllum blepharistes
Bulbophyllum umbellatum
Bulbophyllum repens
Bulbophyllum maxillarioides
Bulbophyllum longissimum
Bulbophyllum longiflorum
CodonosiphonBulbophyllum codonanthum
CodonosiphonBulbophyllum raulersoniae
DesmosanthesBulbophyllum croceum
Bulbophyllum drymoda
EpicranthesBulbophyllum epicranthes
Bulbophyllum lepidum
Bulbophyllum eublepharon
GongorodesBulbophyllum digitatum
Bulbophyllum hemisterranthum
Bulbophyllum hirtulum
Bulbophyllum restrepia
Bulbophyllum grandiflorum
Bulbophyllum infundibuliforme
Bulbophyllum attenuatum
Bulbophyllum imitator
Bulbophyllum roseopictum
LemniscataBulbophyllum lemniscatum
LeopardinaeBulbophyllum leopardinum
LepanthantheBulbophyllum lepanthiflorum
Bulbophyllum amplebracteatum
MacrocauliaBulbophyllum ovalifolium
Bulbophyllum macrourum
Bulbophyllum minutissimum
Bulbophyllum striatellum
Bulbophyllum tortuosum
Bulbophyllum crabro
MonosepalumBulbophyllum muricatum
OxysepalaBulbophyllum clandestinum
Bulbophyllum papulipetalum
Bulbophyllum papuanum
Bulbophyllum absconditum
Bulbophyllum peltopus
Bulbophyllum phreatiopse
Physometra Bulbophyllum physometrum
Planibulbus Bulbophyllum planibulbe
PiestobulbonBulbophyllum piestobulbon
Bulbophyllum plumatum
Bulbophyllum tenuifolium
PseudopelmaBulbophyllum pseudopelma
Bulbophyllum careyanum
RhinantheraBulbophyllum wrayi
Bulbophyllum saurocephalum
Bulbophyllum schistopetalum
SerpenticaulisBulbophyllum wolfei
SestochilosBulbophyllum lobbii
Bulbophyllum gibbosum
TapeinoglossumBulbophyllum centrosemiflorum
Bulbophyllum oblongum
Bulbophyllum tripudians
Bulbophyllum ochroleucum

Ecology

Pollination

Many Bulbophyllum species have the typical odor of rotting carcasses, and the flies they attract assist in their reproduction through pollination.[6] Nevertheless, some species with mild and pleasant floral fragrance attract Dacini fruit flies (particularly Bactrocera and Zeugodacus species) via methyl eugenol, raspberry ketone or zingerone that also act as floral reward during pollination.[19] [20] [21] [22] [23]

To facilitate pollinarium removal and pollinia deposition, this group of orchids, particularly those that attract Dacini fruit flies, possesses a highly modified dynamic lip mechanism - either hinged or see-saw or spring lip (kept either in a close- or open-position depending on resupinate or non-resupinate flower, respectively). When an attracted fly has aligned itself to the opened lip, further probing, feeding and movement towards the lip base result in the lip to snap close, thereby, forcibly tipping the fly in to the column cavity to initiate pollinarium removal or pollinia deposition.[24] [25] [26]

Use in horticulture

Bulbophyllum (abbreviated Bulb. in the horticultural trade)[27] includes species that have been the focus of orchid collectors for over a century. The plants require high humidity combined with good air movement and most of them are ever-blooming - flowering continuously throughout the year. They grow best at moderate light levels, but do not thrive in deep shade. They are considered moderate-to-difficult to cultivate, and require a controlled growing environment to achieve some degree of success. They are not typically suitable as houseplants, and most will not thrive in a Wardian case unless they receive adequate air movement.

The plants' growth habit produces widely spaced pseudobulbs along cord-like rhizome sections, and most of these plants are best accommodated on plaques. Some species in this genus can get very large, but most are small to medium-sized epiphytes from warm, moist, humid tropical forests. They can grow continuously year round with no apparent dormancy period if they are kept warm, are moderate feeders in cultivation, and must be kept moist all the time. They can tolerate dryness for short periods, but they have fine root systems which require moist conditions all the time.[28]

Some of the smaller species do well in pots with small-diameter bark substrate. The plants produce very fine roots generally, and the roots are easily damaged. The plants react poorly to disturbance of their roots. They are easy to maintain once a good environment is established with high humidity and a fresh, buoyant, lightly circulating atmosphere being critical. Most of these species cannot tolerate cold temperatures or freezing.[28]

The flowers produce various odors resembling sap, urine, blood, dung, carrion, and, in some species, fragrant fruity aromas. Most are fly-pollinated, and attract hordes of flies. Bulbophyllum beccarii in bloom has been likened to smelling like a herd of dead elephants and both this species and Bulbophyllum fletcherianum are variously described as making it difficult to walk into a greenhouse in which they are being cultivated if the plants are in bloom because of their overpowering floral odors.[28]

Species

See main article: List of Bulbophyllum species. Some species are known for their extreme vegetative and floral forms:

Conservation status

Some Bulbophyllum species are threatened with extinction, and are recognised as such by the World Conservation Union (IUCN):

Bibliography

External links

Notes and References

  1. David G. Frodin . 2004 . History and concepts of big plant genera . . 53 . 3 . 753–776 . 4135449 . 10.2307/4135449.
  2. Web site: Weston . Peter H. . Genus Bulbophyllum . Royal Botanic Garden Sydney . 5 December 2018.
  3. Web site: Groeneveld . Zoe P. . Jones . David L. . Bulbophyllum . 12 May 2023.
  4. Book: Emly S. Siegerist. Bulbophyllums and their allies: a grower's guide . Timber Press. Portland (OR). 2001. 978-0-88192-506-7.
  5. Book: Thouars . Louis-Marie . Histoire particulière des plantes orchidées recueillies sur les trois Iles Australes d'Afrique, de France, de Bourbon et de Madagascar . 1822 . Paris . 93–110 . 5 December 2018 . 10.5962/bhl.title.492.
  6. Book: Dressler, Robert L.. The Orchids, Natural History and Classification. 0-674-87526-5. 1990. Harvard University Press .
  7. Book: Quattrocchi . Umberto . CRC world dictionary of plant names : common names, scientific names, eponyms, synonyms, and etymology . 2000 . CRC Press . Boca Raton, Florida . 0849326753 . 372.
  8. Web site: Drymoda . Plants of the World Online . 18 July 2021.
  9. Web site: Drymoda . World Checklist of Selected Plant Families . 18 July 2021.
  10. Chase . Mark W. . Cameron . Kenneth M. . Freudenstein . John V. . Pridgeon . Alec M. . Salazar . Gerardo . van den Berg . Cássio . Schuiteman . André . An updated classification of Orchidaceae . Botanical Journal of the Linnean Society . 2015 . 177 . 2 . 151–174 . 10.1111/boj.12234. free .
  11. Web site: Drymoda digitata . Plants of the World Online . 18 July 2021.
  12. Web site: Drymoda gymnopus . Plants of the World Online . 18 July 2021.
  13. Web site: Drymoda latisepala . Plants of the World Online . 18 July 2021.
  14. Web site: Drymoda picta . Plants of the World Online . 18 July 2021.
  15. Web site: Drymoda siamensis . Plants of the World Online . 18 July 2021.
  16. Gamisch, A., Comes, H.P. Clade-age-dependent diversification under high species turnover shapes species richness disparities among tropical rainforest lineages of Bulbophyllum (Orchidaceae). BMC Evol Biol 19, 93 (2019). https://doi.org/10.1186/s12862-019-1416-1
  17. Gamisch . Alexander . Comes . Hans Peter . Clade-age-dependent diversification under high species turnover shapes species richness disparities among tropical rainforest lineages of Bulbophyllum (Orchidaceae) . BMC Evolutionary Biology . Springer Science and Business Media LLC . 19 . 1 . 2019-04-24 . 1471-2148 . 10.1186/s12862-019-1416-1 . 93. 31014234 . 6480529 . free . 2019BMCEE..19...93G .
  18. Smidt . Eric C. . Borba . Eduardo L. . Gravendeel . Barbara . Fischer . Gunter A. . van den Berg . Cássio . Molecular phylogeny of the Neotropical sections of Bulbophyllum (Orchidaceae) using nuclear and plastid spacers . Taxon . Wiley . 60 . 4 . 2011 . 0040-0262 . 10.1002/tax.604009 . 1050–1064.
  19. 10.1023/A:1005477926244. 2000. Tan. Keng-Hong. Journal of Chemical Ecology. 26. 2. 533–546. Nishida. Ritsuo. Mutual reproductive benefits between a wild orchid, Bulbophyllum patens, and Bactrocera fruit flies via a floral synomone. 24971928.
  20. Tan . Keng-Hong . Nishida . R . Synomone or kairomone?--Bulbophyllum apertum flower releases raspberry ketone to attract Bactrocera fruit flies. . Journal of Chemical Ecology . March 2005 . 31 . 3 . 497–507 . 15898497. 10.1007/s10886-005-2023-8 . 2005JCEco..31..497K . 39173699 .
  21. Tan . Keng Hong. Tan . Lin Tze . Nishida . Ritsuo . Floral Phenylpropanoid Cocktail and Architecture of Bulbophyllum vinaceum Orchid in Attracting Fruit Flies for Pollination . Journal of Chemical Ecology . 3 November 2006 . 32 . 11 . 2429–2441 . 10.1007/s10886-006-9154-4. 17082990 . 2006JCEco..32.2429T. 15812115.
  22. Tan. K.H.. 2009. Fruit fly pests as pollinators of wild orchids. Orchid Digest. 73. 3. 180–187.
  23. Nakahira . Masataka . Ono . Hajime . Wee . Suk Ling . Tan . Keng Hong . Nishida . Ritsuo . Floral synomone diversification of Bulbophyllum sibling species (Orchidaceae) in attracting fruit fly pollinators . Biochemical Systematics and Ecology . December 2018 . 81 . 86–95 . 10.1016/j.bse.2018.10.002. 2018BioSE..81...86N . 2433/235528 . 91933950 . free .
  24. Tan, K. H. 2009. Fruit fly pests as pollinators of wild orchids. Orchid Digest, 73(3): 180-187.
  25. Tan, K.H. and Nishida R, 2015 Pollination of bactrocerophilous Bulbophyllum Orchids. pp. 273-279. Proceedings of the 20th World Orchid Conference, Singapore, 2011. Singapore Botanic Gardens.
  26. Tan, K.H. and Tan, L.T. (2018) Movements of floral parts and roles of the tooth on column wall of Bulbophyllum praetervisum (Orchidaceae) flower for pollination by Dacini fruit flies (Diptera: Tephritidae). Journal of Pollination Ecology, 24(17): 157-163.
  27. https://www.rhs.org.uk/plants/pdfs/plant-registration-forms/orchid-name-abbreviations-list.pdf Alphabetical List of Standard Abbreviations for Natural and Hybrid Generic Names
  28. Illustrated Encyclopedia of Orchids