Orchids naturalized in Florida
DOI:
https://doi.org/10.15517/sjs8k094Keywords:
Eulophia, horticulture, naturalization barriers, orchid floras, ornamental trade, pollinators, ZeuxineAbstract
Florida’s naturalized orchids are mostly terrestrials (10/15, 5/10 epiphytes), horticultural escapes (14/15), native to Asia (10/15), tropical American (4/10), and Africa (1/15). Only 3 species are widespread in Florida, Eulophia graminea, Eulophia maculata, and Zeuxine strateumatica, and can be considered invasive based on their spread beyond the areas of their initial establishments. Most of the other orchid species occur in one or two counties and have spread little so are considered naturalized but not invasive. The longest naturalized orchids (5/15) escaped more than 50 years ago, another group (5/10) more than 20 years ago, while the most recently naturalized species (5/10) less than 20 years ago. The 15 naturalized orchids comprise 12% (15/117 species) of Florida’s orchid flora, which is higher than most other places except for Hawaii’s (18/21) which has only 3 native orchids. Most orchids naturalized in Florida (10/15) have also naturalized elsewhere in the world. Failure to reproduce is the reason why most orchids don’t naturalize. To attempt to understand how Florida’s 15 naturalized orchids have overcome this barrier, the literature was examined to learn what their breeding systems and pollinators are in their native areas. This enabled predictions to be made about how these orchids reproduce in Florida. Four of the orchids need no pollinators because they are autogamous or apomictic. The native region pollinators of two of the orchids occur in Florida, five of the orchids are probably pollinated by congeneric species of their native area pollinators (Apis, Centris and Xylocopa), Two of the orchids are pollinated by close analogues of their native area pollinators (butterflies and hummingbirds). Overcoming other barriers to their naturalization, such as the lack of suitable mycorrhizal fungi or the inability to deal with abiotic limitations, has occurred but are poorly known and understood.
Downloads
References
Adit, A., Koul, M., Choudhary, A. K., & Tandon, R. (2022). Interaction between Cymbidium aloifolium and Apis cerana: Incidence of an outlier in modular pollination network of oil flowers. Ecology and Evolution, 12(3), e8697. DOI: https://doi.org/10.1002/ece3.8697
Ackerman, J. (2007). Invasive orchids: weeds we hate to love? Lankesteriana, 7, 19–21. DOI: https://doi.org/10.15517/lank.v7i1-2.18386
Ackerman J. D., Phillips, R. D., Tremblay, R. L., Reiter, N., Karremans, A., Peter, C. I., Bogarin, D., Perez-Escobar, O. A., Liu, H. (2025). Beyond the various contrivances by which orchids are pollinated: global patterns in orchid pollination biology (1.4.0) [Data set]. Zenodo. https://doi.org/10.5281/zenodo.18208949 [Accessed 28 April 2026].
Ackerman, J. D., & González-Orellana, N. (2021). Explosive range expansion of Eulophia graminea (Orchidaceae) in Puerto Rico and the West Indies. Lankesteriana, 21(3), 307–312. DOI: https://doi.org/10.15517/lank.v21i3.48871
Ackerman, J. D., Phillips, R. D., Tremblay, R. L., Karremans, A., Reiter, N., Peter, C. I., Bogarín, D., Perez-Escobar, O. A., & Liu, H. (2023). Beyond the various contrivances by which orchids are pollinated: global patterns in orchid pollination biology. Botanical Journal of the Linnean Society, 202 (3), 295–324. DOI: https://doi.org/10.1093/botlinnean/boac082
Ackerman, J. D., Recart, W., Soifer, L., Falcón, W., & Baider, C. (2024). Invasions of the bamboo orchid: performance variability on islands oceans apart. Biological Invasions, 26(12), 4229–4243. DOI: https://doi.org/10.1007/s10530-024-03442-y
Ames, O. (1938). Zeuxine strateumatica in Florida. Botanical Museum Leaflets, Harvard University, 6(3), 37–45. DOI: https://doi.org/10.5962/p.168390
Bayman, P., Mosquera-Espinosa, A. T., Saladini-Aponte, C. M., Hurtado-Guevara, N. C., & Viera-Ruiz, N. L. (2016). Age-dependent mycorrhizal specificity in an invasive orchid, Oeceoclades maculata. American Journal of Botany, 103(11), 1880–1889. DOI: https://doi.org/10.3732/ajb.1600127
Bierzychudek P. (1981). Asclepias, Lantana, and Epidendrum: a floral mimicry complex? Biotropica 13 Supplement: 54–58. DOI: https://doi.org/10.2307/2388070
Blackburn, T. M., Pyšek, P., Bacher, S., Carlton, J. T., Duncan, R. P., Jarošík, V., Wilson, J. R., & Richardson, D. M. (2011). A proposed unified framework for biological invasions. Trends in ecology & evolution, 26(7), 333–339. DOI: https://doi.org/10.1016/j.tree.2011.03.023
Bogarín, D., Serracín, Z., Samüdiü, Z., Rincón, R., & Püpülin, F. (2014). An updated checklist of the Orchidaceae of Panama. Lankesteriana, 14(3), 135–364. DOI: https://doi.org/10.15517/lank.v14i3.17958
Bory, S., Catrice, O., Brown, S., Leitch, I. J., Gigant, R., Chiroleu, F., Grisoni, M., Duval, M. F., & Besse, P. (2008). Natural polyploidy in Vanilla planifolia (Orchidaceae). Genome, 51(10), 816–826. DOI: https://doi.org/10.1139/G08-068
Brown, P. M. (2002). Wild orchids of Florida (self published)
Bug Guide. (2026). Florida moth and caterpillar - Syntomeida epilais (https://www.bugguide.net/node/view/855457/bgimage/ [Accessed 28 January 2026].
Buragohain, B., Chaturvedi, S. K., & Puro, N. (2016). Pollination Biology of Phaius tankervilleae (Banks ex L’Herit) Bl.(Orchidaceae). International Journal of Plant. Reproductive Biology, 8(1), 75–81.
Cen, T. I. (2016). Un posible polinizador de Laelia rubescens Lindl. (Orchidaceae) en Yucatán, México. Desde el Herbario CICY 8,132–135.
Chung, M. Y., & Chung, M. G. (2005). Pollination biology and breeding systems in the terrestrial orchid Bletilla striata. Plant Systematics and Evolution, 252(1), 1–9. DOI: https://doi.org/10.1007/s00606-004-0256-6
Daehler, C. C. (1998). The taxonomic distribution of invasive plants: ecological insights and comparison to agricultural weeds. Biological Conservation, 84, 167–184. DOI: https://doi.org/10.1016/S0006-3207(97)00096-7
Dematteis, M., & Daviña, J. R. (1999). Chromosome studies on some orchids from South America. Selbyana, 20, 235–238.
Dorcas, M. E., Willson, J. D., Reed, R. N., Snow, R. W., Rochforad, M. R., Miller, M. A., Meshaka, W. E., Andreadis, P. T., Mazzotti, F. J., Romagosa, C. M., & Hart, K. M. (2012). Severe mammal declines coincide with proliferation of invasive Burmese pythons in Everglades National Park. Proceedings of the National Academy of Sciences, 109(7), 2418–2422. DOI: https://doi.org/10.1073/pnas.1115226109
Downing, J. L., Liu, H., McCormick, M. K., Arce, J., Alonso, D., & Lopez-Perez, J. (2020). Generalized mycorrhizal interactions and fungal enemy release drive range expansion of orchids in southern Florida. Ecosphere, 11(8), e03228. DOI: https://doi.org/10.1002/ecs2.3228
Esperón, P. E., & Sauleda, R. P. (2012). Encyclia rufa (Lindley) Britton & Millspaugh in Cuba. New World Orchidaceae–Nomenclatural Notes, 1. (rsauleda.tripod.com)
Fernando, S. S., & Ormerod, P. (2008). An annotated checklist of the orchids of Sri Lanka. Rheedea, 18(1), 1–28. DOI: https://doi.org/10.22244/rheedea.2008.18.01.01
Gallagher, R. V., Randall, R. P., & Leishman, M. (2015). Trait differences between naturalized and invasive plant species independent of residence time and phylogeny. Conservation Biology, 29(2), 360–369. DOI: https://doi.org/10.1111/cobi.12399
Givnish, T. J., Spalink, D., Ames, M., Lyon, S. P., Hunter, S. J., Zuluaga, A., Iles, W. J., Clements, M. A., Arroyo, M. T., Leebens-Mack, J., & Endara, L. (2015). Orchid phylogenomics and multiple drivers of their extraordinary diversification. Proceedings of the Royal Society B: Biological Sciences. 282(1814), 2015.1553. DOI: https://doi.org/10.1098/rspb.2015.1553
González-Díaz, N., & Ackerman, J. D. (1988). Pollination, fruit set, and seed production in the orchid, Oeceoclades maculata. Lindleyana 3(3), 150–155.
Gallaher, T.J., Brock, K., Kennedy, B.H., Imada, C.T., Imada, K., & Walvoord, N. (2020). Plants of Hawai´i. Retrieved from http://www.plantsofhawaii.org. Accessed 19 April 2026.
iNaturalist. (2019). Retrieved from https://www.inaturalist.org/observations/35587453. [Accessed 28 April 2026].
iNaturalist. (2022). Retrieved from https://www.inaturalist.org/observations/139224349. [Accessed 28 April 2026].
iNaturalist. (2026). Retrieved from https://www.inaturalist.org/observations?place_id=18&subview=map&taxon_id=427629. [Accessed 28 April 2026].
Jepson’s eflora. (2026). Retrieved from https:/w.w.w.ucjeps.berkeley.edu/eflora/ [Accessed 20 January 2026].
Kinlock, N. L., Adams, D. W., Dawson, W., Essl, F., Kartesz, J., Kreft, H., Nishino, M., Pergl, J., Pyšek, P., Weigelt, P.. & Kleunen, M. V. (2025). Naturalization of ornamental plants in the United States depends on cultivation and historical land cover context. Ecography, 2025(12), p.e07748. DOI: https://doi.org/10.1002/ecog.07748
Laroche, F. B., & Ferriter, A. P. (1992). The rate of expansion of melaleuca in South Florida. Journal of Aquatic Plant Management. 30, 62–65.
Lin, T. P., & Liu, H. Y. (2025). Annotated checklist of the native orchids of Taiwan and their type information. Tawana, 70(1), 87–124.
Liu, H., & Pemberton, R. W. (2010). Pollination of an invasive orchid (Cyrtopodium polyphyllum) by an invasive oil-collecting bee (Centris nitida) in southern Florida. Canadian Journal of Botany, 88, 290–295. DOI: https://doi.org/10.1139/B10-017
Lubinsky, P., Van Dam, M., & Van Dam, A. (2006). Pollination of Vanilla and evolution in Orchidaceae. Lindleyana, 75(12), 926–929.
Matsuda, Y., & Sugiura, N. (2019). Specialized pollination by honeybees in Cymbidium dayanum, a fall–winter flowering orchid. Plant Species Biology, 34(1), 19–26. DOI: https://doi.org/10.1111/1442-1984.12231
McCartney, C. (2010) Aliens among us: foreign orchids go wild in South Florida. Orchids, 79(10), 576–585.
Mujica, E., & González, E. (2015) A new checklist of orchid species from Cuba. Lankesteriana 15(3), 219–269. DOI: https://doi.org/10.15517/lank.v15i3.22613
Neiland, M. R., & Wilcock, C. C. (1998). Fruit set, nectar reward, and rarity in the Orchidaceae. American Journal of Botany, 85(12), 1657–1671. DOI: https://doi.org/10.2307/2446499
Pansarin, L. M., Pansarin, E. R., & Sazama, M. (2008). Facultative autogamy in Cyrtopodium polyphyllin (Orchidaceae) through a rain-assisted pollination mechanism. Australian Journal of Botany, 56(4), 363–367. DOI: https://doi.org/10.1071/BT07135
Pemberton, R. W., & Ferriter, A. P. (1998). Old World Climbing Fern (Lygodium microphyllum), a dangerous invasive Weed in Florida. American Fern Journal. 88(4), 165–175. DOI: https://doi.org/10.2307/1547769
Pemberton, R. W. (2007). Invasive orchid bee, Euglossa virilism, pollinates the ornamental orchid (Guarianthe skinneri) in Florida. Lankesteriana, 7, 46–468.
Pemberton, R. W. (2008). Pollination of the ornamental Oncidium sphacelatum by the naturalized oil-collecting bee (Centris nitida) in Florida. Selbyana, 29, 87–91. DOI: https://doi.org/10.1653/0015-4040(2008)091[0101:NOTOCB]2.0.CO;2
Pemberton, R., Collins, T., & Koptur, S. (2008). An Asian orchid, Eulophia graminea Orchidaceae: Cambodia), naturalizes in Florida. Lankesteriana 8, 5–14. DOI: https://doi.org/10.15517/lank.v0i0.7946
Pemberton, R. W., & Liu, H. (2009). Marketing time predicts naturalization of horticultural plants. Ecology 90, 69–80. DOI: https://doi.org/10.1890/07-1516.1
Pemberton, R. W., & Liu, H. (2011). Yellow cow horn orchid, Cyrtopodium flavum, spreading in Florida. Journal of the Botanical Research Institute of Texas 5, 331–335.
Pemberton, R. W. (2013). Rapid spread of the alien orchid Eulophia graminea in Florida. Selbyana, 31, 47–51.
Pemberton, R. W. Wheeler, G. R., & Madeira, P. T. (2023). Bee (Hymenoptera: Apidae) pollination of Vanilla planifolia in Florida and their potential in commercial production. Florida Entomologist, 106, 230–237. DOI: https://doi.org/10.1653/024.106.0404
Pemberton, R. W., & Downing, J. L. (2025). Naturalization of Cymbidium aloifolium in Florida. Lankesteriana 25, 135–143. DOI: https://doi.org/10.15517/hpb0yr65
Peter, C. I. (2009). Pollination, floral deception and evolutionary processes in Eulophia (Orchidaceae) and its allies. Doctoral dissertation, University of KwaZulu-Natal, Pietermaritzburg.
Plants of the World Online (POWO). (2026). Facilitated by the Royal Botanic Gardens, Kew. Retrieved from https://powo.science.kew.org/ [Accessed 3 March 2025].
Quezada-Euán, J. J. G., Guerrero-Herrera, R. O., González-Ramírez, R. M., & MacFarlane, D. W. (2024). Frequency and behavior of Melipona stingless bees and orchid bees (Hymenoptera: Apidae) in relation to floral characteristics of vanilla in the Yucatán region of Mexico. Plos one, 19(7), e0306808. DOI: https://doi.org/10.1371/journal.pone.0306808
Recart, W., Ackerman, J. D., & Cuevas, A. A. (2013). There goes the neighborhood: apparent competition between invasive and native orchids mediated by a specialist florivorous weevil. Biological invasions, 15(2), 283–293. DOI: https://doi.org/10.1007/s10530-012-0283-0
Robinson, D. J., Gandy, E., VanHoek, C., & R. W. Pemberton. (2011). Naturalization of the nun’s hood orchid (Phaius tankervilleae) in central Florida. Botanical Research Institute of Texas, 5, 337–339.
Sabapathy, A. U. (2019). Monopterus albus (Asian swamp eel). CABI Compendium. Retrieved from https://www.cabitdigitallibrary.org/doi/10.1079/cabicompendium 17114/ [Accessed 28 January 2026]. DOI: https://doi.org/10.1079/cabicompendium.74114
SERNEC (2026). Southeast Regional Network of Expertise and Collections. Retrieved from https://w.w.w.sernecportal.org/portal/collections/list.php/ [Accessed 25 January 2026].
Small, J. K. (1933). Flora of the Southeastern United States.
Sosa, V. (1992). Systematic studies of Bletia (Orchidaceae). Doctor dissertation, University of California, Berkeley.
Sugiura, N. (1995). The pollination ecology of Bletilla striata (Orchidaceae). Ecological Research, 10(2), 171–177. DOI: https://doi.org/10.1007/BF02347939
Sun, M. (1997). Genetic diversity in three colonizing orchids with contrasting mating systems. American Journal of Botany, 84, 224–232. DOI: https://doi.org/10.2307/2446084
Te Beest, M., Le Roux, J. J., Richardson, D. M., Brysting, A. K., Suda, J., Kubešová, M., & Pyšek, P. (2012). The more the better? The role of polyploidy in facilitating plant invasions. Annals of botany, 109(1), 19-45. DOI: https://doi.org/10.1093/aob/mcr277
Trapnell, D. W., & Hamrick, J. L. (2004). Partitioning nuclear and chloroplast variation at multiple spatial scales in the neotropical epiphytic orchid, Laelia rubescens. Molecular Ecology, 13(9), 2655-2666. DOI: https://doi.org/10.1111/j.1365-294X.2004.02281.x
United States Fish and Wildlife Service. (2014). Devil fire fish (Pterois miles) Ecological Risk Summary Screening. Retrieved from web.archive.org/web/20240903204409/https:/www.fws.gov/sites/default/files/documents/Ecological-Risk-Screening-Summary-Devil-Firefish.pdf/ [Accessed 27 January 2026].
Wetterer, S. K., & Wetterer, J. K. (2022). Spread of the African spotted orchid Oeceoclades maculata in the New World. Lankesteriana, 22(3), 215–224. DOI: https://doi.org/10.15517/lank.v22i3.53113
Wunderlin, R. P., Hansen, B. F., Franck, A. R., & Essig, F. B. (2025). Atlas of Florida Plants. http;//florida. plantatlas.usf.edu/ accessed 25 January 2025.
Published
Issue
Section
License
Copyright (c) 2026 Lankesteriana: International Journal on Orchidology

This work is licensed under a Creative Commons Attribution-NonCommercial-NoDerivatives 3.0 Unported License.
According to the Open Access policy promoted by the University of Costa Rica, all the papers published by Lankesteriana are licensed under the Creative Commons copyright and can be downloaded free of charge. The journal holds copyright and publishing rights under the CC BY-NC-ND 3.0 CR license.
Before the publication of the materials submitted by the author(s) in LANKESTERIANA, the author(s) hereby assign all rights in the article to the Lankester Botanical Garden.



