Rubiaceae

The Rubiaceae are a family of flowering plants, commonly known as the coffee, madder, or bedstraw family. It consists of terrestrial trees, shrubs, lianas, or herbs that are recognizable by simple, opposite leaves with interpetiolar stipules. The family contains about 13,500 species in 611 genera, which makes it the fourth-largest angiosperm family. Rubiaceae has a cosmopolitan distribution, however, the largest species diversity is concentrated in the (sub)tropics.[1] Economic importance includes Coffea, the source of coffee, Cinchona, the source of quinine used to treat malaria, some dye plants (e.g. Rubia), and ornamental cultivars (e.g. Gardenia, Ixora, Pentas).

Description

The Rubiaceae are morphologically easily recognizable as a coherent group by a combination of characters: opposite leaves that are simple and entire, interpetiolar stipules, tubular sympetalous actinomorphic corollas and an inferior ovary.

A wide variety of growth forms are present: shrubs are most common, but members of the family can also be trees, lianas, or herbs. Some epiphytes are also present (e.g. Myrmecodia). The leaves are simple, undivided, and entire; leaf blades are usually elliptical, with a cuneate base and an acute tip. In three genera (Pavetta, Psychotria, Sericanthe), bacterial leaf nodules can be observed as dark spots or lines on the leaves. The phyllotaxis is usually decussate, rarely whorled (e.g. Fadogia), or rarely alternate resulting from the suppression of one leaf at each node (e.g. Sabicea sthenula). Characteristic for the Rubiaceae is the presence of stipules that are mostly fused to an interpetiolar structure on either side of the stem between the opposite leaves. Their inside surface often bears glands called "colleters", which produce mucilaginous compounds protecting the young shoot. The "whorled" leaves of the herbaceous Rubieae tribe have classically been interpreted as true leaves plus interpetiolar leaf-like stipules. The inflorescence is a cyme, rarely of solitary flowers (e.g. Rothmannia), and is either terminal or axillary and paired at the nodes. The flowers are usually bisexual and usually epigynous. The perianth is usually biseriate, although the calyx is absent in some taxa (e.g. Theligonum). The calyx has four or five sepals with basally fused lobes. The corolla is sympetalous with four or five lobes, mostly actinomorphic, usually tubular, often white but also yellow, blue, and (rarely) red. They have four or five stamens, which are alternipetalous and epipetalous. Anthers are longitudinal in dehiscence, but some genera are poricidal (e.g. Rustia). The gynoecium is syncarpous with an inferior ovary (rarely secondarily superior, e.g. Gaertnera, Pagamea[2]). Placentation is axial, rarely parietal (e.g. Gardenia); ovules are anatropous to hemitropous, unitegmic, with a funicular obturator, one to many per carpel. Nectaries are often present as a nectariferous disk atop the ovary. The fruit is a berry, capsule, drupe, or schizocarp. Red fruits are fairly dominant; yellow, orange, or blackish fruits are equally common; blue fruits are rather exceptional save in the Psychotrieae and associated tribes. Most fruits are about 1.0 cm in diameter; very small fruits are relatively rare and occur in herbaceous tribes; very large fruits are rare and confined to the Gardenieae. The seeds are endospermous.[3][4]

Distribution and habitat

Rubiaceae have a cosmopolitan distribution and are found in nearly every region of the world, except for extreme environments such as the polar regions and deserts. The distribution pattern of the family is very similar to the global distribution of plant diversity overall. However, the largest diversity is distinctly concentrated in the humid tropics and subtropics. An exception is the Rubieae tribe, which is cosmopolitan but centered in temperate regions. Only a few genera are pantropical (e.g. Ixora, Psychotria), many are paleotropical, while Afro-American distributions are rare (e.g. Sabicea). Endemic rubiaceous genera are found in most tropical and subtropical floristic regions of the world. The highest number of species is found in Colombia, Venezuela, and New Guinea. When adjusted for area, Venezuela is the most diverse, followed by Colombia and Cuba.[5]

The Rubiaceae consist of terrestrial and predominantly woody plants. Woody rubiaceous shrubs constitute an important part of the understorey of low- and mid-altitude rainforests. Rubiaceae are tolerant of a broad array of environmental conditions (soil types, altitudes, community structures, etc.) and do not specialize in one specific habitat type (although genera within the family often specialize).

Ecology

Flower biology

Most Rubiaceae are zoophilous. Entomophilous species produce nectar from an epigynous disk at the base of the corolla tube to attract insects. Ornithophily is rare and is found in red-flowered species of Alberta, Bouvardia, and Burchellia. Anemophylous species are found in the tribes Anthospermeae and Theligoneae and are characterized by hermaphroditic and/or unisexual flowers that exhibit a set of specialized features, such as striking sexual dimorphism, increased receptive surface of the stigmas and pendulous anthers.[3]

Although most Rubiaceae species are hermaphroditic, outbreeding is promoted through proterandry and spatial isolation of the reproductive organs. More complex reproductive strategies include secondary pollen presentation, heterodistyly, and unisexual flowers.
Secondary pollen presentation (also known as stylar pollen presentation or ixoroid pollen mechanism) is especially known from the Gardenieae and related tribes. The flowers are proterandrous and the pollen is shed early onto the outside of the stigmas and/or the upper part of the style, which serve as a 'receptaculum pollinis'. Increased surface area and irregularity of the pollen receptacle, caused by swellings, hairs, grooves or ridges often ensure a more efficient pollen deposition. After elongation of the style, animals transport the pollen to flowers in the female or receptive stage with exposed stigmatic surfaces. A pollen catapult mechanism is present in the genera Molopanthera and Posoqueria (tribe Posoquerieae) that projects a spherical pollen mass onto visiting sphingidae.[6]
Heterodistyly is another mechanism to avoid inbreeding and is widely present in the Rubiaceae family.[7] The tribes containing the largest number of heterostylous species are Spermacoceae and Psychotrieae. Heterostyly is absent in groups that have secondary pollen presentation (e.g. Vanguerieae).
Unisexual flowers also occur in Rubiaceae and most taxa that have this characteristic are dioecious. The two flower morphs are however difficult to observe as they are rather morphologically similar; male flowers have a pistillode with the ovaries empty and female flowers have empty, smaller anthers (staminodes).[3] Flowers that are morphologically hermaphrodite, but functionally dioecious are for example found in Pyrostria.[8]

Fruit biology

The dispersal units in Rubiaceae can be entire fruits, syncarps, mericarps, pyrenes or seeds. Fleshy fruit taxa are probably all (endo)zoochorous (e.g. tribes Pavetteae, Psychotrieae), while the dispersal of dry fruits is often unspecialized (e.g. tribes Knoxieae, Spermacoceae). When seeds function as diaspores, the dispersal is either anemochorous or hydrochorous. The three types of wind-dispersed diaspores in Rubiaceae are dust seeds (rare, e.g. Lerchea), plumed seeds (e.g. Hillia), and winged seeds (e.g. Coutarea). Long-distance dispersal by ocean currents is very rare (e.g. the seashore tree Guettarda speciosa). Other dispersal mechanisms are absent or at least very rare. Some Spermacoceae having seeds with elaiosomes are probably myrmecochorous (e.g. Spermacoce hepperiana). Epizoochorous taxa are limited to herbaceous Rubiaceae (e.g. Galium aparine fruits are densely covered with hooked bristly hairs).

Associations with other organisms

The genera Anthorrhiza, Hydnophytum, Myrmecodia, Myrmephytum, and Squamellaria are succulent epiphytes that have evolved a mutualistic relationship with ants. Their hypocotyl grows out into an ant-inhabited tuber.[9] Some shrubs or trees have ant holes in their stems (e.g. Globulostylis).[10]
Some Rubiaceae species have domatia that are inhabited by mites (viz. acarodomatia; e.g. Plectroniella armata).[11]
An intimate association between bacteria and plants is found in three rubiaceous genera (viz. Pavetta, Psychotria, and Sericanthe).[12] The presence of endophytic bacteria is visible by eye because of the formation of dark spots or nodules in the leaf blades. The endophytes have been identified as Burkholderia bacteria. Their function, however, remains enigmatic. A different type of plant-bacteria association is found in the genera Fadogia, Fadogiella, Globulostylis, Rytigynia, Vangueria (all belonging to the Vanguerieae tribe), where bacteria are found freely distributed among the mesophyll cells and no leaf nodules are formed.[13][14][15]

Systematics

The Rubiaceae family is named after Rubia, a name used by Pliny the Elder in his Naturalis Historia for madder (Rubia tinctorum).[16] The roots of this plant have been used since ancient times to extract alizarin and purpurin, two red dyes used for coloring clothes. The name rubia is therefore derived from the Latin word ruber, meaning red. The well-known genus Rubus (blackberries and raspberries) is unrelated and belongs to Rosaceae, the rose family.

Taxonomy

The family was described in 1789 by Antoine Laurent de Jussieu.[17]

Several historically accepted families are since long included in Rubiaceae: Aparinaceae, Asperulaceae, Catesbaeaceae, Cephalanthaceae, Cinchonaceae, Coffeaceae, Coutariaceae, Galiaceae, Gardeniaceae, Guettardaceae, Hameliaceae, Hedyotidaceae, Houstoniaceae, Hydrophylacaceae, Lippayaceae, Lygodisodeaceae, Naucleaceae, Nonateliaceae, Operculariaceae, Pagamaeaceae, Psychotriaceae, Randiaceae, Sabiceaceae, Spermacoceaceae.[1]
More recently, the morphologically quite different families Dialypetalanthaceae,[18] Henriqueziaceae,[19] and Theligonaceae[20][21][22] were reduced to synonymy of Rubiaceae.

Subfamilies and tribes

The classical classification system of Rubiaceae distinguished only two subfamilies: Cinchonoideae, characterized by more than one ovule in each locule, and Coffeoideae, having one ovule in each locule.[23][24] This distinction, however, was criticized because of the distant position of two obviously related tribes, viz. Gardenieae with many ovules in Cinchonoideae and Ixoreae with one ovule in Coffeoideae, and because in species of Tarenna the number of ovules varies from one to several in each locule.[25][26] During the twentieth century other characters were used to delineate subfamilies, e.g. stylar pollen presentation, raphides, endosperm, heterostyly, etc. On this basis, three[27] or eight[28] subfamilies were recognised. The last subfamilial classification solely based on morphological characters divided Rubiaceae into four subfamilies: Cinchonoideae, Ixoroideae, Antirheoideae, and Rubioideae.[3] In general, problems of subfamilies delimitation in Rubiaceae based on morphological characters are linked with the extreme naturalness of the family, hence a relatively low divergence of its members.[3]

The introduction of molecular phylogenetics in Rubiaceae research has corroborated or rejected several of the conclusions made in the pre-molecular era. There is support for the subfamilies Cinchonoideae, Ixoroideae, and Rubioideae, although differently circumscribed, and Antirheoideae is shown to be polyphyletic.[29] The tribe Coptosapelteae including the genera Acranthera and Coptosapelta, and the monogeneric tribe Luculieae have not been placed within a subfamily and are sister to the rest of Rubiaceae.[30] Currently, in most molecular research concerning the Rubiaceae family, the classification with three subfamilies (Cinchonoideae, Ixoroideae, and Rubioideae) is followed.[31] However, an alternative view is proposed where only two subfamilies are recognized, an expanded Cinchonoideae (that includes Ixoroideae, Coptosapeltaeae and Luculieae) and Rubioideae.[22] The adoption of the Melbourne Code for botanical nomenclature had an unexpected impact on many names that have been long in use and are well-established in literature. According to the Melbourne Code, the subfamilial name Ixoroideae should be replaced by Dialypetalanthoideae.[32] However, Dialypetalanthus is morphologically quite aberrant in Rubiaceae and if it should be excluded from Rubiaceae, the subfamilial name remains Ixoroideae. Molecular studies also have substantial impact on tribal delimitations and taxonomic changes are still being made.[33][34] Also here, according to the Melbourne Code, the tribe Condamineeae should be renamed to Dialypetalantheae. The following list contains the validly published tribe names, however, some tribes might be disputed. The approximate number of species is indicated between brackets,[35] however, several genera and species are not yet placed in a tribe.

Genera

For a comprehensive list, see List of Rubiaceae genera.

The Rubiaceae family contains about 13,500 species in 611 genera. This makes it the fourth-largest family of flowering plants by number of species and fifth-largest by number of genera. Although taxonomic adjustments are still being made, the total number of accepted genera remains stable. In total, around 1300 genus names have been published, indicating that more than half of the published names are synonyms. Psychotria, with around 1850 species, is the largest genus within the family and the third-largest genus of the angiosperms, after the legume Astragalus and the orchid Bulbophyllum. However, the delimitation of Psychotria remains problematic and its adjustment might reduce the number of species. In total, 30 genera have more than 100 species. However, 136 genera are monotypic, which account for 22% of all genera, but only for 1.1% of all species.[5]

Phylogeny

Molecular studies have demonstrated the phylogenetic placement of Rubiaceae within the order Gentianales and the monophyly of the family is confirmed.[36][37] The relationships of the three subfamilies of Rubiaceae together with the tribes Coptosapelteae and Luculieae are shown in the phylogenetic tree below. The placement of these two groups relative to the three subfamilies has not been fully resolved.[37]

Rubiaceae

Rubioideae




Ixoroideae



Cinchonoideae





Coptosapelteae



Luculieae




Evolution

The fossil history of the Rubiaceae goes back at least as far as the Eocene. The geographic distribution of these fossils, coupled with the fact that they represent all three subfamilies, is indicative of an earlier origin for the family, probably in the Late Cretaceous or Paleocene. Although fossils dating back to the Cretaceous and Palaeocene have been referred to the family by various authors, none of these fossils has been confirmed as belonging to the Rubiaceae.[38]

The oldest confirmed fossils, which are fruits that strongly resemble those of the genus Emmenopterys, were found in the Washington and are 48–49 million years old. A fossil infructescence and fruit found in 44 million-year-old strata in Oregon was assigned to Emmenopterys dilcheri, an extinct species. The next-oldest fossils date to the Late Eocene and include Canthium from Australia, Faramea from Panama, Guettarda from New Caledonia, and Paleorubiaceophyllum, an extinct genus from the southeastern United States.[38]

Fossil Rubiaceae are known from three regions in the Eocene (North America north of Mexico, Mexico-Central America-Caribbean, and Southeast Pacific-Asia). In the Oligocene, they are found in these three regions plus Africa. In the Miocene, they are found in these four regions plus South America and Europe.[38]

Uses

Food

Staple foods are not found in the Rubiaceae; instead, some species are consumed locally and fruits may be used as famine food. Examples are African medlar fruits (e.g. V. infausta, V. madagascariensis), African peach (Nauclea latifolia), and noni (Morinda citrifolia).

Beverage

The most economically important member of the family and the world's second-most important commodity (after petroleum) is the genus Coffea used in the production of coffee. Coffea includes 124 species, but only three species are cultivated for coffee production: C. arabica, C. canephora, and C. liberica.[5]

Medicinal

The bark of trees in the genus Cinchona is the source of a variety of alkaloids, the most familiar of which is quinine, one of the first agents effective in treating malaria. Woodruff (Galium odoratum) is a small herbaceous perennial that contains coumarin, a natural precursor of warfarin, and the South American plant Carapichea ipecacuanha is the source of the emetic ipecac. Psychotria viridis is frequently used as a source of dimethyltryptamine in the preparation of ayahuasca, a psychoactive decoction.[39] The bark of the species Breonadia salicina have been used in traditional African medicine for many years.[40] The leaves of the Kratom plant (Mitragyna speciosa) contain a variety of alkaloids, including several psychoactive alkaloids and is traditionally prepared and consumed in Southeast Asia, where it has been known to exhibit both painkilling and stimulant qualities, behaving as a μ-opioid receptor agonist, and often being used in traditional Thai medicine in a similar way to and often as a replacement for opioid painkillers like morphine.

Ornamentals

Originally from China, the common gardenia (Gardenia jasminoides) is a widely grown garden plant and flower in frost-free climates worldwide. Several other species from the genus are also seen in horticulture. The genus Ixora contains plants cultivated in warmer-climate gardens; the most commonly grown species, Ixora coccinea, is frequently used for pretty red-flowering hedges. Mussaenda cultivars with enlarged, colored calyx lobes are shrubs with the aspect of Hydrangea; they are mainly cultivated in tropical Asia. The New Zealand native Coprosma repens is a commonly used plant for hedges. The South African Rothmannia globosa is seen as a specimen tree in horticulture. Nertera granadensis is a well-known house plant cultivated for its conspicuous orange berries. Other ornamental plants include Mitchella, Morinda, Pentas, and Rubia.

Dyes

Rose madder, the crushed root of Rubia tinctorum, yields a red dye, and the tropical Morinda citrifolia yields a yellow dye.

Culture

Image gallery

References

  1. 1 2 "Angiosperm Phylogeny Website". Retrieved June 2014.
  2. Igersheim A, Puff C, Leins P, Erbar C (1994). "Gynoecial development of Gaertnera Lam. and of presumably allied taxa of the Psychotrieae (Rubiaceae): secondary 'superior' vs. inferior ovaries". Botanische Jahrbücher fur Systematik 116: 401–414.
  3. 1 2 3 4 5 Robbrecht E (1988). "Tropical woody Rubiaceae". Opera Botanica Belgica 1: 1–271.
  4. Takhtajan A (2009). Flowering Plants (2 ed.). Springer. ISBN 978-1-4020-9608-2.
  5. 1 2 3 Davis AP, Govaerts R, Bridson DM, Ruhsam M, Moat J, Brummitt NA (2009). "A global assessment of distribution, diversity, endemism, and taxonomic effort in the Rubiaceae". Annals of the Missouri Botanical Garden 96 (1): 68–78. doi:10.3417/2006205.
  6. Delprete PG (2009). "Taxonomic history, morphology, and reproductive biology of the tribe Posoquerieae (Rubiaceae, Ixoroideae)". Annals of the Missouri Botanical Garden 96 (1): 79–89. doi:10.3417/2006192.
  7. Anderson WR (1973). "A morphological hypothesis for the origin of heterostyly in the Rubiaceae". Taxon 22 (5/6): 537–542. doi:10.2307/1218628.
  8. Bridson DM (1987). "Studies in African Rubiaceae-Vanguerieae: a new circumscription of Pyrostria and a new subgenus, Canthium subgen. Bullockia". Kew Bulletin 42: 611–639. doi:10.2307/4110068.
  9. Kapitany A (2007). Australian succulent plants: an introduction. Boronia, Victoria: Kapitany Concepts. pp. 144–155. ISBN 0-646-46381-0.
  10. Verstraete B, Lachenaud O, Smets E, Dessein S, Sonké B (2013). "Taxonomy and phylogeny of Cuviera (Rubiaceae-Vanguerieae) and reinstatement of the genus Globulostylis with the description of three new species". Botanical Journal of the Linnean Society 173 (3): 407–441. doi:10.1111/boj.12062.
  11. Tilney PM, van Wyk AE, van deer Merwe CF (2012). "Structural evidence in Plectroniella armada (Rubiaeae) for possible material exchange between domatia and mites". PLoS ONE 7 (7): e39984. doi:10.1371/journal.pone.0039984.
  12. Lemaire B, Vandamme P, Merckx V, Smets E, Dessein S (2011). "Bacterial leaf symbiosis in angiosperms: host specificity without co-speciation". PLoS ONE 6 (9): e24430. doi:10.1371/journal.pone.0024430.
  13. Verstraete B, Van Elst D, Steyn H, Van Wyk B, Lemaire B, Smets E, Dessein S (2011). "Endophytic bacteria in toxic South African plants: identification, phylogeny and possible involvement in gousiekte". PLoS ONE 6 (4): e19265. doi:10.1371/journal.pone.0019265.
  14. Verstraete B, Janssens S, Smets E, Dessein S (2013). "Symbiotic beta-proteobacteria beyond legumes: Burkholderia in Rubiaceae". PLoS ONE 8 (1): e55260. doi:10.1371/journal.pone.0055260.
  15. Verstraete B, Janssens S, Lemaire B, Smets E, Dessein S (2013). "Phylogenetic lineages in Vanguerieae (Rubiaceae) associated with Burkholderia bacteria in sub-Saharan Africa". American Journal of Botany 100: 2380–2387. doi:10.3732/ajb.1300303.
  16. Simpson MG (2006). Plant Systematics (1 ed.). Elsevier Academic Press. ISBN 978-0-12-644460-5.
  17. de Jussieu AL (1789). Genera plantarum : secundum ordines naturales disposita, juxta methodum in horto regio parisiensi exaratam, anno M.DCC.LXXIV. Paris. OCLC 5161409.
  18. Fay MF, Bremer B, Prance GT, van der Bank M, Bridson D, Chase MW (2000). "Plastid rbcL sequence data show Dialypetalanthus to be a member of Rubiaceae". Kew Bulletin 55 (4): 853–864. doi:10.2307/4113630.
  19. Rogers GK (1981). "The wood of Gleasonia, Henriquezia, and Platycarpum (Rubiaceae) and its bearing on their classification: some new considerations". Brittonia 33 (3): 461–465. doi:10.2307/2806441.
  20. Wunderlich R (1971). "Die systematische Stellung von Theligonum". Österreichische botanische Zeitschrift 119: 329–394. doi:10.1007/bf01377490.
  21. Rutishauser F, Ronse Decraene LP, Smets E, Mendoza-Heuer I (1998). "Theligonum cynocrambe: developmental morphology of a peculiar rubiaceous herb". Plant Systematics and Evolution 210 (1): 1–24. doi:10.1007/BF00984724.
  22. 1 2 Robbrecht E, Manen J-F (2006). "The major evolutionary lineages of the coffee family (Rubiaceae, angiosperms). Combined analysis (nDNA and cpDNA) to infer the position of Coptosapelta and Luculia, and supertree construction based on rbcL, rps16, trnL-trnF and atpB-rbcL data. A new classification in two subfamilies, Cinchonoideae and Rubioideae". Systematic Geography of Plants 76: 85–146.
  23. Hooker JD (1873). "Ordo LXXXIV. Rubiaceae". In Bentham G, Hooker JD. Genera planetarium ad exemplaria imprimis in herbaria kewensibus servata defirmata 2. London. pp. 7–151.
  24. Schumann K (1891). "Rubiaceae". In Engler A, Prantl K. Die natürlichen Pflanzenfamilien 4. Leipzig: Engelmann. pp. 1–156.
  25. Baillon H (1878). "Sur les limits du genre Ixora". Adansonia 12: 213–219.
  26. Solereder H (1893). "Ein Beitrag zur anatomischen Charakteristik und zur Systematik deer Rubiaceen". Bull. Herb. Boissier 1: 167–183.
  27. Verdcourt B (1958). "Remarks on the classification of the Rubiaceae". Bulletin du Jardin botanique de l'état, Bruxelles 28: 209–281. doi:10.2307/3667090.
  28. Bremekamp CEB (1966). "Remarks on the position, the delimitation and the subdivision of the Rubiaceae". Acta Botanica Neerlandica 15: 1–33. doi:10.1111/j.1438-8677.1966.tb00207.x.
  29. Bremer B, Andreasen K, Olsson D (1995). "Subfamilial and tribal relationships in the Rubiaceae based on rbcL sequence data". Annals of the Missouri Botanical Garden 82: 383–397. doi:10.2307/2399889.
  30. Rydin C, Kainulainen K, Razafimandimbison SG, Smedmark JEE, Bremer B (2009). "Deep divergences in the coffee family and the systematic position of Acranthera". Plant Systematics and Evolution 278: 101–123. doi:10.1007/s00606-008-0138-4.
  31. Bremer B (2009). "A review of molecular phylogenetic studies of Rubiaceae". Annals of the Missouri Botanical Garden 96 (1): 4–26. doi:10.3417/2006197.
  32. Reveal JL (2012). "Newly required infrafamilial names mandated by changes in the code of nomenclature for algae, fungi and plants". Phytoneuron 33: 1–32.
  33. Kainulainen K, Razafimandimbison SG, Bremer B (2013). "Phylogenetic relationships and new tribal delimitations in subfamily Ixoroideae (Rubiaceae)". Botanical Journal of the Linnean Society 173 (3): 387–406. doi:10.1111/boj.12038.
  34. Mouly A, Kainulainen K, Persson C, Davis AP, Wong KM, Razafimandimbison SG, Bremer B (2014). "Phylogenetic structure and clade circumscriptions in the Gardenieae complex (Rubiaceae)". Taxon 63 (4): 801–818. doi:10.12705/634.4.
  35. "the World Checklist of Rubiaceae". Retrieved March 2016.
  36. Bremer B, Bremer K, Heidari N, Erixon P, Olmstead RG, Anderberg AA, Källersjö M, Barkhordarian E (2002). "Phylogenetics of asteroids based on 3 coding and 3 non-coding chloroplast DNA markers and the utility of non-coding DNA at higher taxonomic levels". Molecular Phylogenetics and Evolution 24: 274–301. doi:10.1016/s1055-7903(02)00240-3.
  37. 1 2 Bremer B, Eriksson T (2009). "Time tree of Rubiaceae: phylogeny and dating the family, subfamilies, and tribes". International Journal of Plant Sciences 170: 766–793. doi:10.1086/599077.
  38. 1 2 3 Graham A (2009). "Fossil record of the Rubiaceae". Annals of the Missouri Botanical Garden 96 (1): 90–108. doi:10.3417/2006165.
  39. Riba J, Valle M, Urbano G, Yritia M, Morte A, Barbanoj MJ (2003). "Human pharmacology of ayahuasca: subjective and cardiovascular effects, monoamine metabolite excretion, and pharmacokinetics". Journal of Pharmacology and Experimental Therapeutics 306 (1): 73–83. doi:10.1124/jpet.103.049882. PMID 12660312.
  40. Neuwinger, Hans Dieter (1994). African Ethnobotany: Poisons and Drugs: Chemistry, Pharmacology, Toxicology. Stuttgart, Germany: Chapman & Hall.

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