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Bromeliaceae

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"Bromeliad" redirects here. For the trilogy of children's books, see The Nome Trilogy.

Bromeliaceae
Pineapple, a bromeliad
Scientific classification
Kingdom:
Plantae
(unranked):
Angiosperms
(unranked):
Monocots
(unranked):
Commelinids
Order:
Poales
Family:
Bromeliaceae

Subfamilies

The Bromeliaceae (the bromeliads) are a family of monocot flowering plants of 51 genera and around 3475 known species[2] native mainly to the tropical Americas, with a few species found in the American subtropics and one in tropical west Africa, Pitcairnia feliciana.[3]

They are among the basal families within the Poales and are unique because they are the only family within the order that has septal nectaries and inferior ovaries.[4] These inferior ovaries characterize the Bromelioideae, a subfamily of the Bromeliaceae.[5] The family includes both epiphytes, such as Spanish moss (Tillandsia usneoides), and terrestrial species, such as the pineapple (Ananas comosus). Many bromeliads are able to store water in a structure formed by their tightly-overlapping leaf bases. However, the family is diverse enough to include the tank bromeliads, grey-leaved epiphyte Tillandsia species that gather water only from leaf structures called trichomes, and a large number of desert-dwelling succulents.

The largest bromeliad is Puya raimondii, which reaches 3–4 m tall in vegetative growth with a flower spike 9–10 m tall, and the smallest is Spanish moss.[citation needed]

Description

Bromeliad

Bromeliads are plants that are adapted to various climates. Foliage takes different shapes, from needle-thin to broad and flat, symmetrical to irregular, spiky to soft. The foliage, which usually grows in a rosette, is widely patterned and colored. Leaf colors range from maroon, through shades of green, to gold. Varieties may have leaves with red, yellow, white and cream variations. Others may be spotted with purple, red, or cream, while others have different colors on the tops and bottoms of the leaves.

The inflorescences produced by bromeliads are also regarded as considerably more diverse than any other plant family. Some flower spikes may reach 10 meters tall, while others only measure 2–3 mm across. Upright stalks may be branched or simple with spikes retaining their color from two weeks up to 12 months, depending on species. In some species, the flower remains unseen, growing deep in the base of the plants.

Root systems vary according to plant type. Terrestrial bromeliad species have complex root systems that gather water and nutrients, while epiphytic bromeliads only grow hard, wiry roots to attach themselves to trees and rocks.

An epiphytic bromeliad
Bromeliad at US Botanic Garden

Some bromeliads are faintly scented, while others are heavily perfumed. Blooms from the species Tillandsia cyanea have a fragrance resembling that of clove spice.

One study found 175,000 bromeliads per hectare (2.5 acres) in one forest; that many bromeliads can sequester 50,000 liters (more than 13,000 gallons) of water.[6]

A wide variety of organisms takes advantage of the pools of water trapped by bromeliads. A study of 209 plants from the Ecuadorian lowlands identified 11,219 animals, representing more than 300 distinct species, many of which are found only on bromeliads. Examples include some species of ostracods, small salamanders about 2.5 cm (0.98 in) in length, and tree frogs. Jamaican bromeliads are home to Metopaulias depressus, a reddish-brown crab 2 cm (0.79 in) across, which has evolved social behavior to protect its young from predation by Diceratobasis macrogaster, a species of damselfly whose larvae live in bromeliads. Some bromeliads even form homes for other species of bromeliads.[6]

Distribution

Bromeliads growing on telephone lines in Bolivia

Plants in the Bromeliaceae are widely represented in their natural climates across the Americas. One species can be found in Africa.[7] They can be found at altitudes from sea level to 4200 meters, from rainforests to deserts. 1814 species are epiphytes, some are lithophytes, and some are terrestrial. Accordingly, these plants can be found in the Andean highlands, from northern Chile to Colombia, in the Sechura Desert of coastal Peru, in the cloud forests of Central and South America, in southern United States from southern Virginia to Florida to Texas, and in far southern Arizona.

Ecology

Bromeliads often serve as phytotelmata, accumulating water between their leaves. The aquatic habitat created as a result is host to a diverse array of invertebrates, especially aquatic insect larvae.[8] These bromeliad invertebrates benefit their hosts by increasing nitrogen uptake into the plant.[9][10][11]

Evolution

Bromeliads are among the more recent plant groups to have emerged. The greatest number of primitive species resides in the Andean highlands of South America, where they originated in the tepuis of the Guyana Shield.[12] The most basal genus, Brocchinia, is endemic to these tepuis, and is placed as the sister group to the remaining genera in the family.[13] The west African species Pitcairnia feliciana is the only bromeliad not endemic to the Americas, and is thought to have reached Africa via long-distance dispersal about 12 million years ago.[12]

Adaptations

Bromeliads are able to live in a vast array of environmental conditions due to their many adaptations. Trichomes, in the form of scales or hairs, allow bromeliads to capture water in cloud forests and help to reflect sunlight in desert environments.[14] Some bromeliads have also developed an adaptation known as the tank habit, which involves them forming a tightly bound structure with their leaves that helps to capture water and nutrients in the absence of a well-developed root system.[14] Bromeliads also use crassulacean acid metabolism (CAM) photosynthesis to create sugars. This adaptation allows bromeliads in hot or dry climates to open their stomates at night rather than during the day, which reduces water loss.[15]

Classification

The family Bromeliaceae is currently placed in the order Poales.

Subfamilies

The family Bromeliaceae is organized into eight subfamilies:[16]

Bromeliaceae were originally split into three subfamilies: Bromelioideae, Tillandsioideae, and Pitcairnioideae based on morphological characters.[17] However, molecular evidence has revealed that while Bromelioideae and Tillandsioideae are monophyletic, Pitcairnioideae is, in fact, paraphyletic[18] and should be split into six subfamilies: Brocchinioideae, Lindamanioideae, Hechtioideae, Navioideae, Pitcairnioideae, and Puyoideae.[19]

Brocchinioideae is defined as the most basal branch of Bromeliaceae based on both morphological and molecular evidence, namely genes in chloroplast DNA.[20]

Lindmanioideae is the next most basal branch distinguished from the other subfamilies by convolute sepals and chloroplast DNA.[21]

Hechtioideae is also defined based on analyses of chloroplast DNA; similar morphological adaptations to arid environments also found in other groups are attributed to convergent evolution.[16]

Navioideae is split from Pitcairnioideae based on its cochlear sepals and chloroplast DNA.[22]

Puyoideae has been re-classified multiple times and its monophyly remains controversial according to analyses of chloroplast DNA.[21]

Genera

  • Billbergia pyramidalis
    Billbergia pyramidalis
  • Billbergia pyramidalis
    Billbergia pyramidalis
  • Tillandsia usneoides hanging from branches
    Tillandsia usneoides hanging from branches
  • The flower of a Billbergia sp.
    The flower of a Billbergia sp.
  • Puya alpestris
    Puya alpestris
  • Flower close-up
    Flower close-up
  • A bromeliad
    A bromeliad
  • Tillandsia airplants mounted on the bark of a cork oak
    Tillandsia airplants mounted on the bark of a cork oak

Cultivation and uses

Humans have been using bromeliads for thousands of years. The Incas, Aztecs, Maya and others used them for food, protection, fiber and ceremony, just as they are still used today. European interest began when Spanish conquistadors returned with pineapple, which became so popular as an exotic food that the image of the pineapple was adapted into European art and sculpture. In 1776, the species Guzmania lingulata was introduced to Europe, causing a sensation among gardeners unfamiliar with such a plant. In 1828, Aechmea fasciata was brought to Europe, followed by Vriesea splendens in 1840. These transplants were so successful, they are still among the most widely grown bromeliad varieties.

In the 19th century, breeders in Belgium, France and the Netherlands started hybridizing plants for wholesale trade. Many exotic varieties were produced until World War I, which halted breeding programs and led to the loss of some species. The plants experienced a resurgence of popularity after World War II. Since then, Dutch, Belgian and North American nurseries have greatly expanded bromeliad production.

Only one bromeliad, the pineapple (Ananas comosus), is a commercially important food crop. Bromelain, a common ingredient in meat tenderizer, is extracted from pineapple stems. Many other bromeliads are popular ornamental plants, grown as both garden and houseplants.

Collectors

Édouard André was a French collector/explorer whose many discoveries of bromeliads in the Cordilleras of South America would be influential on horticulturists to follow. He served as a source of inspiration to 20th-century collectors, in particular Mulford B. Foster and Lyman Smith of the United States and Werner Rauh of Germany and Michelle Sullivan of Australia.[23]

See also

References

  1. ^ Angiosperm Phylogeny Group (2009), "An update of the Angiosperm Phylogeny Group classification for the orders and families of flowering plants: APG III", Botanical Journal of the Linnean Society, 161 (2): 105–121, doi:10.1111/j.1095-8339.2009.00996.x, retrieved 2010-12-10
  2. ^ Christenhusz, M. J. M.; Byng, J. W. (2016). "The number of known plants species in the world and its annual increase". Phytotaxa. 261 (3). Magnolia Press: 201–217. doi:10.11646/phytotaxa.261.3.1. {{cite journal}}: Unknown parameter |lastauthoramp= ignored (|name-list-style= suggested) (help)
  3. ^ Mabberley, D.J. (1997). The Plant Book. Cambridge: Cambridge University Press.
  4. ^ Judd, Walter S. Plant systematics a phylogenetic approach. 3rd ed. Sunderland, MA: Sinauer Associates, Inc., 2007.
  5. ^ Sajo, M. G. "Floral anatomy of Bromeliaceae, with particular reference to the epigyny and septal nectaries in commelinid monocots." Plant Systematics and Evolution 247 (2004): 215-31.
  6. ^ a b "Pineapple Dreams", The Wild Side, Olivia Judson, The New York Times, March 18, 2008
  7. ^ Porembski, Stefan; Barthlott, Wilhelm (1999). "PITCAIRNIA FELICIANA: THE ONLY INDIGENOUS AFRICAN BROMELIAD". Harvard Papers in Botany. 4 (1): 175–184. JSTOR 41761298.
  8. ^ Frank, J. H.; Lounibos, L. P. (2009-02-01). "Insects and allies associated with bromeliads: a review". Terrestrial Arthropod Reviews. 1 (2): 125–153. doi:10.1163/187498308X414742. ISSN 1874-9836. PMC 2832612. PMID 20209047.
  9. ^ Ngai, Jacqueline T.; Srivastava, Diane S. (2006-11-10). "Predators Accelerate Nutrient Cycling in a Bromeliad Ecosystem". Science. 314 (5801): 963–963. doi:10.1126/science.1132598. ISSN 0036-8075. PMID 17095695.
  10. ^ Leroy, Céline; Corbara, Bruno; Dejean, Alain; Céréghino, Régis (2009-09-01). "Ants mediate foliar structure and nitrogen acquisition in a tank-bromeliad". New Phytologist. 183 (4): 1124–1133. doi:10.1111/j.1469-8137.2009.02891.x. ISSN 1469-8137.
  11. ^ Romero, Gustavo Q.; Srivastava, Diane S. (2010-09-01). "Food-web composition affects cross-ecosystem interactions and subsidies". Journal of Animal Ecology. 79 (5): 1122–1131. doi:10.1111/j.1365-2656.2010.01716.x. ISSN 1365-2656.
  12. ^ a b Givnish, Thomas J., Kendra C. Millam, Timothy M. Evans, Jocelyn C. Hall, J. C. Pires, Paul E. Berry, and Kenneth J. Sytsma. "Ancient vicariance or recent long-distance dispersal? Inferences about phylogeny and South American-African disjunctions in Raptaceae and Bromeliaceae based on ndhf sequence data." International Journal of Plant Science 165.4 (2004): 35-54.
  13. ^ Barfuss, Michael H., Rosabelle Samuel, Walter Till, and Todd F. Stuessy. "Phylogenetic relationships in subfamily Tillandsioideae (Bromeliaceae) based on DNA sequence data from seven plastid regions." American Journal of Botany 92.2 (2005): 337-51.
  14. ^ a b Schulte, Katharina, Michael H. Barfuss, and Georg Zizka. "Phylogeny of Bromelioideae (Bromeliaceae) inferred from nuclear plastid DNA loci reveals the evolution of the tank habit within the subfamily." Molecular Phylogenetics and Evolution 51 (2009): 327-39.
  15. ^ Rex, Martina, Kerstin Patzolt, Katharina Schulte, Georg Zizka, Roberto Vasquuez, Pierre L. Ibisch, and Kurt Weising. "AFLP analysis of genetic relationships in the genus Fosterella L.B. Smith (Pitcairnioideae, Bromeliaceae)." Genome 50 (2007): 90-105.
  16. ^ a b Givnish, Thomas (2007). "Phylogeny, adaptive radiation, and historical biogeography of Bromeliaceae inferred from ndhF sequence data". Aliso: A Journal of Systematic and Evolutionary Botany.
  17. ^ Smith LB, Downs RJ (1974). "Flora neotropica: monograph. 14.(Bromeliaceae)". New York Botanical Garden.
  18. ^ Terry, Randall (1997). "Examination of subfamilial phylogeny in Bromeliaceae using comparative sequencing of the plastid locus ndhF". American Journal of Botany.
  19. ^ Zanella, Camila (2012). "Genetics, evolution and conservation of Bromeliaceae". Genetics and Molecular Biology.
  20. ^ Horres, Ralf (2000). "Molecular phylogenetics of Bromeliaceae: evidence from trnL (UAA) intron sequences of the chloroplast genome". Plant Biology.
  21. ^ a b Givnish, Thomas (2011). "Phylogeny, adaptive radiation, and historical biogeography in Bromeliaceae: insights from an eight-locus plastid phylogeny". American Journal of Botany.
  22. ^ Crayn, Darren (2004). "Multiple origins of crassulacean acid metabolism and the epiphytic habit in the Neotropical family Bromeliaceae". Proceedings of the National Academy of Sciences.
  23. ^ André, Édouard François. "Bromeliaceae Andreanae. Description et histoire des Bromeliacees recoltees dans La Colombie, L'Ecuador et Le Venezuela". Paris: Librairie Agricole; G. Masson, 1889
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