Because of taxonomic revision, as the family size (in terms of genera and species) differs according to the time period of study; so, too, does the family's higher-level relationships, includingorder. Burseraceae is a genetically-supportedmonophyletic group sinceAPG III and is frequently cited within theSapindales. It is recognized as asister group to theAnacardiaceae.
The Burseraceae are characterized by the generally non-allergenic resin they produce in virtually all plant tissue and their distinctive smooth, yet flaking, aromatic bark.[4][5] The origins of the family can be traced to thePaleocene (about 65 Mya) whenBeiselia mexicana first diverged inMexico.[1] The subsequent divergences in the family lineage and migration of species in theEocene (53 Mya) out of North America have led to the current distribution of the species being primarily associated with the tropics.[1] Though the family likely originated in North America, the greatest genetic diversity presently is found in the Southern Hemisphere.[1]Tabonuco (Dacryodes excelsa) andgumbo limbo (Bursera simaruba) represent the economic, ethnobotanical, and ecological significance of the Burseraceae in the Western Hemisphere, while frankincense (Boswellia sacra) and myrrh (Commiphora myrrha) represent the same in the Eastern Hemisphere.
The Burseraceaetrees orshrubs are characterized byresins (havingtriterpenoids and ethereal oils)[6] that are present within the plant tissue from the vertical resin canals and ducts in thebark to the leaf veins.[4][5][7][8][9] In fact, thesynapomorphy of the Burseraceae is the smooth yet peeling or flaking aromatic bark.[4][5] The clear, nonallergenic[4] resins may smell like almonds,[5] but at least the most well known resins, frankincense and myrrh, have a distinct odor. The leaves are generally alternate, spiral, and odd-pinnately compound with opposite, frequently long-petiolulate, entire to serrate, pinnately veinedleaflets whose symmetry is distinctive in some genera.[4][5] However, some members are known to have trifoliate or unifoliate leaves.[4] The leaf and leaflet stalks and axis may be brown and scurfy, while the leaf base is swollen and may be concave adaxially.[5] The family members tend to be withoutstipules.[4][8] The determinate, axillaryinflorescences carry small, radial, unisexual flowers.[4][8] The plants tend to bedioecious.[4][8] The flowers may have four or five faintlyconnate butimbricatesepals with an equal number of distinct, imbricatepetals.[4][8] Also, the stamens, that may containnectar discs, have distinct glabrousfilaments that occur in one or two whorls and in numbers equaling or twice the number of petals; the tricolporatepollen is contained within twolocules of theanthers that open longitudinally along slits.[4] Thegynoecium contains 3–5 connatecarpels, onestyle, and one stigma that is head-like to lobed.[4] Each locule of the superior ovary has twoovules with axile placentation that are anatropous to campylotropous.[4] The one- to five-pittedfruit is adrupe that opens at maturity.[4] The endosperm is usually lacking in the embryo.[4]
Some discrepancy exists in the literature about the size of the Burseraceae. Records say that the family has 17[4][8][9] to 18[1][7] genera and 500[4][8] to 540[9] to 726 species.[1] Other authors cite different numbers: 16–20 genera and 600 species;[6] 20 genera and 500–600 species;[10] According to a pollen studies and molecular data, the family is split into threetribes: the Protieae, Bursereae, and Canarieae. The Protieae are composed ofProtium (147 species and largest in this tribe),Crepidospermum, Garuga, andTetragastris.[7] The Bursereae, which are further split intosubtribes Boswelliinae and Burserinae, containCommiphora (nearly 200 species and largest in the family),Aucoumea, Beiselia, Boswellia, Bursera, andTriomma.[7] Finally, the Canarieae are composed ofCanarium (75 species and largest in this tribe),Dacryodes, Haplolobus, Pseudodacryodes, Rosselia, Santiria, Scutinanthe, andTrattinnickia.[7] The morphology of the fruit, which is a drupe, helps to distinguish between the three tribes.[8][9] Though the groupings have slightly changed since the 1990s, the Protieae are described as having a two- to five-parted drupe[9] with either ‘free or adhering parts’ which are ‘not fused in the endocarp’;[8] The Bursereae are described as having a drupe with parts that are fused in theendocarp, but anexocarp with dehiscing valves;[8][9] and the Canarieae as simply having a drupe with parts that are fused in the endocarp.[8][9]
This is a list of the 19 genera of the Burseraceae with placement in threetribes (and subtribes where applicable):[1]
According to the literature, the Burseraceae have not been lumped with other families nor split up into several others. However, they have "jumped" orders several times. For example, in the early 19th century, the family seems to have been placed in theBurserales, with theAnacardiaceae andPodoaceae.[12] In the mid-19th century and early 20th century, the family was placed in theGeraniales.[7][10] Then, by the mid- and late-20th century, the family was moved to theRutales.[7] Finally, in the late 20th century, the family was (and today still is) located within the Sapindales.[7] Families that are consistently found in the same order as the Burseraceae (except when in the Burserales) include theRutaceae,Meliaceae, andSimaroubaceae.[7] Only in recent studies were the Burseraceae and theAnacardiaceae seen as sister groups.[7]
TheSapindales are contained within themalvids of therosidclade within theeudicotyledons.[4] The order contains nine[4][5] to 15 families,[13] 460 genera,[5] and from 5,400[13] to 5,670[5] to 5,800 species.[4] The currently recognized families include Aceraceae, Anacardiaceae, Burseraceae, Hippocastanaceae, Julianaceae, Meliaceae, Rutaceae, Sapindaceae, and Simaroubaceae. The Sapindales are a clade supported by DNA-based analyses onrbcL,atpB, and 18S sequences.[4] Within the Sapindales are two clades that contain gum and resin: the Rutaceae-Meliaceae-Simaroubaceae clade and the Burseraceae-Anacardiaceae clade.[5] The Burseraceae are thus not the only family in the Sapindales with this characteristic. Thesynapomorphies of the clade include pinnately compound alternately- or spirally-arranged leaves that may be palmately compound, trifoliate, or unifoliate, and small four- or five-merous flowers having a characteristic nectar disk and imbricate petals and sepals.[4] Some of these characteristics also occur in theRosales.[13] However, the Sapindales and Rutales may actually form a complex, since many families "jump" between them. Indeed,rbcL sequence studies seem to indicate that a sapindalean/rutalean complex exists and may better represent the relationships of the families than the separate orders would.[13] A study based on thechloroplast-encodedgenerbcL reconstructed cladograms that include families within both the Sapindales and Rutales. One suchcladogram indicated that the Sapindales are robust and that the Burseraceae (and Anacardiaceae) are within a single clade of their own.[13] This grouping seems to make sense, as both the Burseraceae and Anacardiaceae have secretory canals in the phloem and resin canals in the leaves, and are unique in the Sapindales for havingbiflavones in the leaf tissue.[4][13][14] However, the two families have several distinguishing characteristics. The resin of the Burseraceae is nonallergenic and two ovules per carpel occur, whereas the resin of the Anacardiaceae can be allergenic or poisonous and one ovule per carpel is found.[1][6] The Burseraceae-Anacardiaceae clade is sister to a robust cluster of three other families, the Sapindaceae-Aceraceae-Hippocastanaceae clade.[13] The Rutaceae-Meliaceae-Simaroubaceae clade is sister to the Burseraceae-Anacardiaceae and Sapindaceae-Aceraceae-Hippocastanaceae clade.[13] TherbcL technique is supported and considered acceptable until such time as other analytical methods become better developed.[13]
The Burseraceae are distributed throughout the world and primarily in the tropics, especiallyMalesia, Africa, and Central and South America.[7][8] The three tribes can be linked to a specific region of the world, although this is not obligatory. For example, members of the tribe Protieae are generally found in South America, those of the Bursereae are found in Africa andMesoamerica, while members of the Canarieae are found in Malesia.[7] However, each tribe has a representative genus present in all the tropical regions:Dacryodes (Canarieae),Protium (Protieae), andCommiphora (Bursereae).[1] The Burseraceae are found in a variety of habitats, including hot, drydesert andsavannah, as well as in coastalmangrove forest andrain forest habitats.[8] One study found that the family originated in North America during thePaleocene (about 65 Mya), when the earliest fossils of the Sapindales are found.[1] During the Early to Middle Eocene (about 53 Mya), family members dispersed to easternLaurasia (i.e. Europe and Asia) via theBoreotropical Land Bridge and the continents in the Southern Hemisphere, which is now the area of the greatest generic diversity of this family.[1]
More specifically, the earliest diverging genus wasBeiselia (of the Bursereae subtribe Boswelliinae) in either North America, Mexico, or theCaribbean in the Paleocene. Similar results from other studies[1][15] find thatBeiselia mexicana, a native of Mexico, is basal to the remaining Burseraceae. These results may indicate that the family originated in Mexico. The next divergence was in the Early Eocene when the Burserinae (i.e.Commiphora) diverged and emigrated from North America into Africa,Madagascar, and India.[1]Commiphora dispersed throughout Africa during the Middle Eocene (about 44 Mya) and from Africa to Madagascar during the Oligocene (about 30 Mya) via the Mozambique Channel Land Bridge; the spread to India was more recent (about 5 Mya).[1] The Canarieae and Boswelliinae (subtribes of Bursereae) dispersed from westernLaurasia and spread eastward during theEocene;fossils of Canarium, for example, from theCzech Republic date to the LateOligocene (23 Mya).[1] Finally, the Protieae originated in North America like the rest of the family, then migrated to Africa and Asia through theTethys seaway in the LateEocene (about 37 Mya), but then made its way back to South America via long-distance dispersal.[1] By the lateOligocene (about 23Mya), all three Burseraceae tribes were extant and dispersed throughout the Northern Hemisphere.[1]
The mechanism of seed dispersal via animal linkvectors (endozoochoric dispersal) may explain how most Burseraceae were able to expand their range so efficiently across the globe.[1]Beiselia, Boswellia, andTriomma have dry fruits better suited for wind dispersal, but most Burseraceae have fleshy, edible fruit that is eaten by many animal dispersers.[1] The seeds may provide a high reward in fat (24–73%) and protein (2.7–25.9%) if digested, but many animals eat just the fleshy part of the fruit and either discard theendocarp right away or excrete it some time later.[1] Some known Burseraceae fruit consumers include hornbills (Buceros bicornis, Ceratogyma atrata, C. cylindricus, Penelopides panini), oilbirds (Steatnoris caripensis), fruit pigeons, warblers, vireos, orioles, flycatchers, tanagers, woodpeckers,loeries, primates (Cercopithecus spp.,Lophocebus albigena), lemurs (Varecia variegate subsp.variegate), and sun bears (Helarctos malayanus).[1] The fruits may also have been water dispersed.[1]
Several representative species within the Burseraceae typify the economic and ethnobotanic significance of the family. First,Dacryodes excelsa of the Canarieae is an important old-growth species found in the Caribbean. Second,Bursera simaruba of the Burserinae is a fast-growing ornamental that is one of a few representatives of the primarily tropical family in the United States. Finally, the namesakes of the familyBoswellia carterii (frankincense) andCommiphora abyssinica (myrrh) are important economically and medicinally in several parts of the world. Though this is a small subset of the large number of potentially important species, these four members exemplify the wide use and importance of the Burseraceae. The latter three are frequently cited in the literature for their renowned importance.
Commonly known as tabonuco (or gommier, also candlewood),Dacryodes excelsa is a large, dominant tree found inPuerto Rico and other parts of the Caribbean.[16] The seeds of the tree are a source of food for birds. Like all members, the tree releases sap from the bark when wounded. The clear sap oozes from the tree and hardens to a white, aromatic waxyresin that can be used to make candles and incense.[16] Before the arrival of the Spaniards to Puerto Rico, the nativeTaínos used the resin to make torches. The wood itself is useful for constructing housing, furniture, boxes, small boats, and a variety of other wood-based products; the utility of the wood is comparable to that ofmahogany andbirch.[16] In addition, species likeCanarium littorale,Dacryodes costata,Santiria laevigata, andSantiria tomentosa from Malaysia, as well asAucoumea klaineana andCanarium schweinfurthii from Africa, also produce valuable wood for construction projects and carpentry.[8]
Several species in the genusCanarium are used as edible fruits (for example,Canarium album, the Chinese olive) and nuts (pili nuts,Canarium ovatum).
Species in the genusBursera, especially theso-called elephant tree, grow primarily in Mexico, where their secretions are a raw material in makingvarnish.[8][10] TheMaya also used aBursera sp. to makeincense.[9] However, theBursera may also be considered an ornamental genus and a common representative of the family in the United States, especially in Florida (B. simaruba) and the Southwest (B. odorata, B. microphylla).[4][10]
Naked Indian (also known as gumbo limbo), orBursera simaruba, in particular, is found inFlorida, Mexico, the Caribbean,Venezuela, andBrazil. The tree is also named the ‘tourist tree’ for its very distinctive flaking red bark; apparently, the tree occurs in tropical areas where many white tourists go on vacation.[17] The resin from this tree can be used to make varnish and turpentine.[17] In addition, the resin may also be used similarly totiger balm (containingCinnamomum camphora of theLauraceae) to relieve sprains and muscle aches.[17] The leaves are used to brew a tea to relieve inflammation.[18] The bark serves as an antidote to skin irritation caused byMetopium toxiferum (also known as poisonwood, Florida poison tree, and hog gum) of the Anacardiaceae. The gumbo limbo grows quickly and can be used to make a living fence especially out of cut limbs that are placed straight into the ground or for restoration projects as apioneer species.[17] The tree is highly tolerant of high-intensity wind such as hurricane-force winds, so is planted in areas where hurricanes occur frequently, such as Florida and the Caribbean. The seeds of this species are also a source of food for birds.
Frankincense, or olibanum, (Boswellia carterii) and myrrh (Commiphora abyssinica) have long been valued for the aromatic resins they produce. These resins are extracted via tapping, or cutting of the bark to make it release sap. The liquid sap hardens and is gathered, sold as is or further processed and mixed with spices, seeds, and roots to make various forms of incense.[19] Both species are native to parts of Northeast Africa (Somalia, frankincense; Somalia andEthiopia, myrrh) andArabia (Oman andYemen, frankincense), but their distribution and use have been extended beyond these regions to India and China.[19] The best frankincense is grown in Oman and the incense is widely used in worship in India.[19] The ancient Egyptians prized frankincense for the resin they used to make the characteristic dark eyeliner and myrrh as an embalming agent for deceasedpharaohs.[19][20] At that time, myrrh was worth more than gold. In modern times resins from these trees are used in Chinese herbal medicine and IndianAyurvedic medicine to treat several ailments. Pills containing small doses of frankincense and other ingredients are valued inoriental medicine for promoting blood flow and the movement of theqi (‘life force’ or ‘spiritual energy’).[19] and myrrh is similarly claimed to promote blood flow, stimulate the stomach and digestion, and to be useful in treating diabetes, menopause, uterine tumors,amenorrhoea, anddysmenorrhea.[19] Both frankincense (containing triterpene acids)[21] and myrrh are used to relieve pain and inflammation as in arthritis and asthma.[19][22]
^abcdefghijklmnopqrstuvWeeks, A., Daly, D.C. and B.B. Simpson. 2005. The phylogenetic history and biogeography of the frankincense and myrrh family (Burseraceae) based on nuclear and chloroplast sequence data. Molecular Phylogenetics and Evolution, 35: 85–101.
^Takhtajan, A. 1997. Diversity and Classification of Flowering Plants. Columbia University Press, New York, New York, USA.
^abcdefghiGadek, P.A., E.S. Fernando, C.J. Quinn, S.B. Hoot, T. Terrazas, MC. Sheahan, and M.W. Chase. 1996. Sapindales: Molecular delimitation and infraordinal groups. Am. J. Bot. 83: 802–811.
^Wannan, B.S., Waterhouse, J.T., Gadek, P.A. and C.J. Quinn. 1985. Biflavonyls and the affinities of Blepharocarya. Biochemical Systematics and Ecology, 13: 105–108.
^Clarkson, J.J., Chase, M.W. and M.M. Harley. 2002. Phylogenetic relationships in Burseraceae based on plastid rps 16 intron sequences. Kew Bull., 57: 183–193.
^Carretero, M.E., Lopez-P., J.L., Abad, M.J., Bermejo, P., Tillet, S., Israel, A. and B. Noguera-P. 2007. Preliminary study of the anti-inflammatory activity of hexane extract and fractions from Bursera simaruba (Linneo) Sarg. (Burseraceae)
^Colombini, M.P., Modugno, F., Silvano, F. and M. Onor. 2000. Characterization of the balm of an Egyptian mummy from the Seventh Century B.C. Studies in Conservation, 45(1): 19–29.
^Banno, N., Akihisa, T., Yasukawa, K., Tokuda, H., Tabata, K., Nakamura, Y., Nishimura, R., Kimura, Y. and T. Suzuki. 2006. Anti-inflammatory activities of the triterpene acids from the resin of Boswellia carteri. Journal of Ethnopharmacology
^Hanus, L.O., Rezanka, T., Dembitsky, V.M. and A. Moussaieff. 2005. Myrrh- Commiphora Chemistry. Biomed. Papers, 149(1): 3–28.