Title: The Burseraceae Family of Flowering Plants
Author: Jillian Vaught
Taxonomy
The Burseraceae family of flowering plants is of
the order Sapindales (“Burseraceae”). Sources report the Burseraceae family to
be composed of at least 16 genera: Aucoumea,
Canarium , Crepidospermum, Dacryodes, Elaphrium, Garguga, Haplolobus, Protium,
Santiria, Tetragastris, Tingulonga, Trattinnickia, and the four well known
genera: Beiselia, Boswellia, Bursera, and
Commiphora. The Plant List, a working list of the known plant species
maintained by efforts of Missouri Botanical Gardens, Kew, and Royal Botanical
Gardens, encompasses 1,870 scientific names of species rank for the Burseraceae
family. Of the 1,870 species rank names, 615 are accepted names of species
(Burseraceae, The Plant List) (Figure
1-1). The Burseraceae family is a monophyletic group, confirmed by molecular
data. (Daly, 2011)
Studies by the Word Pollen and Spore Flora have
worked to incorporate pollen morphology of Burseraceae into the classification
of three tribes: Protieae, Bursereae, and Canarieae. Within these three tribes,
the morphology of the pollen grain is being used to classify the tribes by pollen
type. Pollen type is delimited by grain polarity, polar outline, length of
polar axis, width of equatorial axis, shape, exine type, exine surface,
apocolpial wall thickness, apocolpial ultrastructure, and the presence or absence
of apocolpial endexine. From these data (Harley, Song, Banks, 2005), 14 pollen
types have been distinguished. Of the 14 types, 9 are unique to Burseraceae.
Seven of the uncommon pollen types are represented by only one taxon and three
of these taxa represent monospecific genera. DNA data has also been used to
support the pollen morphology that Bursera
and Commiphora share a close
relationship as well as Garuga and Boswellia. At this time, most of the
pollen grain types are limited to Burseraceae of the tribe Protieae. Pollen
grain types for the tribes Bursereae and Canarieae have not been published
(Harley, Song, and Banks, 2005).
The Burseraceae family is
commonly called the Torchwood family or Incense family for their aromatic sap
or resin. Of the 16 genera, Commiphora
is the largest genus encompassing nearly 200 species. Commiphora is most commonly recognized as the "Myrrh"
genus, while Boswellia is recognized
as the "Frankincense" genus. The genus Bursera is economically important for its reddish-brown wood
(Dimmitt, 2014). Its economic importance makes it key to investigation by
ecologists who endeavor to preserve biological habitats from consumption.
Ecologists working with Burseraceae commonly encounter taxonomic challenges.
Molecular and phylogenetic analysis shows Bursera
and Commiphora to be closely related.
In this regard, placing species between the two genuses has been reason for
debate especially in the case of South American species C. leptophloeos. By pollen morphology and geographic location, C. leptophloeos is placed in the Commiphora genus; however, new molecular
data suggests it is most closely related to Bursera.
Taxonomic difficulties such as this are commonly encountered within the
Burseraceae family as molecular data becomes increasingly available (Rosell and
Olson, 2010).
A few genera, such as Bursera, have been separated into
subclades. Bursera has four major
subclades: Simaruba, Microphylla, Fragilis, and Fagaroides. Species are subject
to rearrangement within the subclades especially within the Fagaroides where
morphological divisions are inconsistent (Rosell and Olson, 2010).
Phylogeny
The crown group of the
Burseraceae is dated 58 million years ago (Presl). Bursera and Commiphora
diverged somewhere between 120 and 60 million years ago and the Commiphora did not completely diversify
until some 32 to 23 million years ago. It is believed that the varying
distribution of these two genera is due to continental drift (Presl).
Phylogenies place the Burseraceae
and Anacardiaceae as sister clades within the Sapindales. Beiselia is a
recently-investigated family that is likely sister to the Burseraceae, having
many sister automorphic features (Daly, 2011). Interestingly, the Burseraceae
family has consistently been placed in the same order as Meliaceae, Rutaceae,
and Simaroubaceae in different systematic placements (Harley, Song, and Banks,
2005).
Weeks and Simpson (2007) tested
the monophyly of Commiphora to
hypothesize the events of its diversification and widespread geography. Using
fossil calibrations, they were able to hypothesize that the success of this
tree was due to post-Paleogene aridification that selected for this dry-adapted
species. Evidence from fossils shows that dry-adapted tropical floras like Commiphora were already present in
Africa prior to the Paleogene; however, their species expanded most likely as a
result of the post-Paleogene climate. Dry-arid climate must hold a key to the
diversity of Commiphora considering
approximately 150 of its 190 species can be found throughout desert and
seasonally dry habitats (Weeks and Simpson, 2007).
Weeks (2005) previously
determined that Commiphora was a
sister to a subgenus of American Bursera
species. Fossil calibrations, DNA analysis of intergenic spacers, and Bayesian
inference from Weeks and Simpson’s analysis suggests that Commiphora is sister to Paleo-tropical Bursera tonkinesis, not
the American Bursera clade. Further
publications on this subject may be able to support the listing of Bursera as an exclusively American
taxon. This new phylogenetic information and genera age via fossil calibrations
of B. tonkinesis are evidence for
intercontinental transfer of Burseraceae from North America to Asia while its
genus Commiphora spread westward to
Africa (Weeks and Simpson, 2007).
Sets of molecular data attained
during Weeks and Simpson’s analysis were used to determine the probability of
relationships among three Burseraceae genera. Nuclear and chloroplasts data
sets were used to assemble maximum parsimony trees for Commiphora, Bursera, and Elaphrium. Age calibration from
fossil-based evidence formed nodes in the trees. The resulting 100 trees were
scored with maximum parsimony, compiling the average age and confidence for
each node. All species were scored based on their presence in the following
regions: Africa, Madagascar, India, southeast Asia, South America, Mexico, and
North America. The results showed that the Commiphora
species monophyly was supported by 100% parsimony bootstrap support and 100%
Bayesian posterior probability. The sister relationship of Commiphora to Paleotropical B.
tonkinensis is 53% parsimony bootstrap support and 94% Bayesian posterior
probability. Both parsimony bootstrap support and Bayesian posterior
probability highly support the sister relationship of Elaphrium, B. tonkinensis, and
Commiphora (Weeks and Simpson, 2007).
Morphological Characteristics
The Burseraceae family includes
trees or shrubs, all of which have resin ducts within the bark containing
triterpenoid compounds and aromatic oils. The Burseraceae are mostly dioecious.
The leaves are alternate or pinnately compound. The inflorescences are usually
axillary, rarely terminal, with paniculate or uniflorous arrangements. The
flowers are actinomorphic having 3-5 sepals which are connate and form a tube at
the base. They may have 3-5 petals that are either free or adnate to the calyx.
The stamens are in 1-2 whorls (equaling or twice the number of petals). The
filaments originate outside the nectar-discs (Salywon, 1999). The ovaries are
superior with about 3 locules, and there are usually 2 ovules per locule. The stigmas
are 2-5 lobed. They produce drupe fruits, with mostly dry mesocarp and 1-5
stoney seeds. The fruits are generally dehiscent with 2-5 valves (Woodson and
Porter, 1970). The seeds commonly have a pseudoaril and always lack endosperm (Salywon,
1999).
Figure 3-1 shows Burseraceae of the species Bursera tomentosa. Bursera is
categorized by tree or shrubs with smooth or rough bark. Thin sheets peel off
of the older bark or in thick scales. The leaves are odd-pinnate or bi-pinnate.
The leaf margins are entire to toothed. Inflorescences appear in axillary
raceme panicles, which usually develop just before the new leaves. The flowers
are usually small and unisexual with 3-5 white or yellowish petals that extend
beyond the sepals. The gynoecium has 2-3 carpels and the ovary is 2-3 lobed.
The endocarp is usually one-seeded with no endosperm (Woodson and Porter, 1970).
The genus Protium can be distinguished by larger leaves of entire leaf
margins. The inflorescences contain flowers of 4-5 free petals that are usually
fleshy with 8-10 stamens. The gynoecium has 4-5 carpels and ovaries of 4-5
lobes. The fruit is globose, ellipsoid, or ovoid with a fleshy and resinous
mesocarp (Woodson and Porter, 1970). Protium
panamense can be seen in Figure 3-2.
Of the three most economically important
genera to be described, Commiphora has
one of the most diverse species populations. It can be a tree or shrub with
smooth bark of various colors that are found to peel easily. The inflorescence
are either paniculate or solitary and in clusters with 4 greenish to yellow
petals. Ovaries are made of 3 locules with 2 ovules in each. The drupe fruit
produces a single stone and seed (Eggi, 2002). Figure 3-3 shows Commiphora campestris.
Plant Geography
The Burseraceae family is most widespread
in tropical America, northwest Africa, and Malaysia. Four genera are known to
grow in Panama: Bursera, Protium,
Tetragastris, and Trattinnickia (Woodson and Porter, 1970). Commiphora grow ideally in arid zones
across sub-Saharan Africa, dominating over 1.6 million square kilometers of the
Acacia-Commiphora woodlands in East Africa (Weeks and Simpson, 2007). Commiphora’s major distribution is over
Africa, Madagascar, India, and South America. Evidence by fossil calibration
and molecular phylogenies suggests that Bursera
and Commiphora spread from west to
east across Laurasia through the North Atlantic boreotropical corridor. Figure 4-1 shows a Commiphora myrrha tree in the arid North African Sahara. Evidence
also suggests that Bursera tonkinensis
was transferred from North America to Asia and expanded westward through Africa
(Weeks and Simpsons, 2007). Figure 4-2
shows the occurrence of Burseraceae across the world.
The Protieae are found primarily
in South America, while the Canarieae tribe are found primarily in Malesia
(Harley, Song, and Banks, 2005). Cultivators have found that Arizona provides
sufficient arid climate to grow Bursera
fagaroides var. elongata and Bursera microphylla (Salywon, 1999). The
popular Frankincense genera Boswellia,
includes species of Boswellia sacra
which are known for their essential oil distilleries in Oman and Yemen. Boswellia carteri from Somalia and Boswellia serrate from India and China
are also common frankincense resinous trees (Suhail and Wu, 2011).
Historical biogeographers take
into account the effects of global cooling during the Miocene period and how it
may have forced tropical species of Commiphora
to migrate toward the equator into their current disjunct distribution in
Africa and the southeast Asian tropics. In the case of the endemic Malagasy
species of Commiphora, biologists
find that they comprise more than two unrelated clades and must result from two
introductions of the species (Weeks and Simpson, 2007).
Economic Importance
The economic importance of the
Burseraceae family extends across the globe from Asia to Africa and back to the
United States. The red-barked Gumbo-Limbo tree (Bursera simaruba), residing in south Florida, produces lightweight
wood that is great for carving. Before molded plastic, B. simaruba wood was used to make carousel horses (Gilman and
Watson, 2006). The wood is still popular for making fishing boats and its
fragrant resin is used as incense (“Burseraceae”).
On the west coast of Africa, the
Gabonese Republic commercially grows Aucoumea
klaineana. A. klaineana is a medium to large evergreen tree with a diameter
anywhere from 30-40 centimeters reaching up to 60 meters tall. This tree makes
up 90 percent of Gabon’s timber production (“Okoume Fact File”, 2013).
The fruit of Drakryodes edulis is commonly traded between Cameroon, Nigeria, and
Gabon. The tree prefers humid lowlands such as those found abundantly in
Cameroon. These trees are grown in tree-farmed areas and have great potential
as an export, as the trees produce a high yield of fruit each year (Ayuk,
Duguma, Franzel, and Kengue, 1999). The fruit is known as “butterfruit” due to
its butter-like pulpy oil. The oil of these fruits has attracted western dietary
attention for its unsaturated oil, high amino acid content, and minerals like
potassium, calcium, and magnesium (Kane, 2010). Figure 5-1 shows a basket of “butterfruit” from Cameroon.
Despite Burseraceae’s use from
its pure biomass, its most sought-after family members may be those of Commiphora and Boswellia. The several known species of Boswellia produce what we commonly call frankincense, the essential
oil extracted from the tree’s oleo-gum resin. (“Burseraceae”) Not only does the
extracted frankincense essential oil show fascinating medical properties, it is
sanctioned as a biblical oil. The resin from Commiphora is used to make myrrh, another biblical oil of medical
importance (“Burseraceae”).
Biological Information
The flowers of Burseraceae are
mostly dioecious. The genera Boswellia,
Garuga, Dacryodes, and Bursera all
have perfect flowers. Commiphora monoica
is one of the rare species that is monoecious. Commiphora samharensis is one of the few speices that undergoes pollination
through selfing (Kubitzki, 2011). Members of the Protium spruceanum in Central Brazil produce abundant nectar as a
pollination reward. On average, the nectar has a 30% concentration of sucrose (Kubitzki,
2011). Small insects pollinate most of the Burseraceae flowers (Kubitzki, 2011).
The family’s most characteristic
trait is the consistency of its oleoresin. The resin contains terpenoids, a
class of organic chemicals with a varying 5-carbon skeleton (Maimone). The
resin is a mixture of volatile and non-volatile terpene chemical compounds that
are most commonly non-volatile in Burseraceae. Biochemists have determined that
the family uses terpenoids as a means of attracting pollinators while its
toxicity repels herbivores (Kubitzki, 2011).
Further investigation into the
chemical compounds that make up the essential oil of the Boswellia genus, shows the isolation of β and α boswellic acid from commercial frankincense
resin. Boswellic acid is a lupine-type
triterpene, a structure that has been determined using chemical and spectral
evidence such as mass spectrometric techniques. Figure 6-1 shows the structure of β and α boswellic acid. The four main
producing species of this resin are Boswellia
carteri, Boswellia frereana, B. sacra, and B. serrate. This acid has only
been isolated from frankincense, or the Boswellia
genus. The isolated contents of boswellic acid appear as a colorless
crystal. Since the acid is confined to Boswellia,
it has been used to identify archaeological samples of frankincense (Culioli,
Mathe, and Archier, 2003).
Frankincense in Medical Research
Frankincense has been highly
valued as a component of alternative medicine practice for centuries. Most of
the frankincense that is traded internationally is distilled into an essential
oil and is from Oman, Yemen, and Somalia (Yousef, 2011). Recently it has
sparked the attention of scientific research for its anti-inflammatory and
anti-neoplastic effects (Suhail and Wu, 2011). In 2011, research conducted by
the University of Oklahoma Health Science Center in Oklahoma City has found the
optimal conditions under which the essential oil of Boswellia sacra induces tumor cell-specific cytotoxicity. In their
research, Urologists and Physiologist of the university assayed the apoptosis
by genomic DNA fragmentation. They then used Western blotting methods to study
the oil-regulated proteins of Boswellia
sacra’s essential oil that were involved in apoptosis. The results were undisputable,
essential oil hydrodistilled at temperatures around 100° C had
the greatest response inducing tumor cell cytotoxicity. These oils distilled at
high temperature also contained the highest molecular weight of boswellic acid.
The research shows that components of the essential oil target and induce cell
death in malignant cells. Ongoing research strives to produce an essential oil
of Boswellia sacra with consistent
chemical composition that can be used for pre-clinical validation of boswellic
acid as a cancer fighting agent (Suhail and Wu, 2011).
Youself (2011) published his
findings on the effect of distilled frankincense extracts given orally to forty
male Wister Albino rates. The experiment shows that after the rats had received
frankincense in their water for 30 days, they showed toxic levels of uric acid
in the blood. The high levels of uric acid the in blood caused a break down of
purine bases in the DNA. In addition, there was an accumulation of creatinine
in the kidney and increased levels of nitric acid that stimulated free radicals
in the surrounding kidney tissue. The biochemical and histological examination
of rats exposed to frankincense concluded that frankincense, as traditional
medicine, must certainly be used with precaution (Yousef, 2011).
From timber to medicine, the
importance of the Burseraceae family is exceptional. Its confirmed presence on
five continents makes it ideal for taxonomic and molecular phylogenetic
research. Its trees and shrubs of papery bark appear in the most uncanny arid
climate. The family’s consistent production of oleoresin from its bark has
survived ancient biblical history and is still being distilled into essential
oils in the Middle East. As an alternative medicine and a source of nutrition,
members of the Burseraceae family continue to support our developing world into
the 21st century.
Figure 1-1 Accepted Species
Names from The Plant List (“Burseraceae”, The Plant List)
The status of the 1,870 species names for the
family Burseraceae recorded in The Plant List, are as follows:
|
Figure 3-1 Bursera tomentosa (Woodson and Porter, 1970)
|
Figure 3-2 Protium panamense (Woodson and Porter, 1970) |
Figure 3-3 Commiphora campestris (Woodson and Porter, 1970) |
Figure 4-1 Commiphora myrrha tree in North African
Sahara. (“Prelude
Medicinal Plants Database”)
|
Figure 4-2 The Occurrence
of Commiphora across the Globe (Presl)
|
Figure 5-1 The
“Butterfruit” of Drakryodes edulis from
Cameroon
(Asaah, 2002)
|
Figure 6-1 a) Structure of
β Boswellic Acid.
(Culioli,
Mathe, and Archier, 2003)
|
Figure
6-1 b) α Boswellic Acid. (Culioli, Mathe, and Archier, 2003)
|
Literature Cited
Asaah, Ebenezer. “African Plum.” West
and Central Africa. World Agroforestry Centre, 2002. Web. 23 Mar. 2014.
<www.fidafrique.net/IMG/pdf/les-prunes.pdf>.
Ayuk, Elian T., Bahiru Duguma, Steve
Franzel, and Joseph Kengue. “Uses, Management, and Economic Potential of
Dacryodes edulis in Cameroon.” Economic Botany. Volume 52, No. 3 (1999):
292-301. JSTOR. Web 23 Mar. 2014.
“Burseraceae.” Encyclopedia
Britannica. Encyclopedia Britannica Online Academic Edition. Encyclopedia
Britannica Inc, 2014. Web. 16 Mar. 2014.
“Burseraceae.” The Plant List.
Version 2 (2011). Web 16 Mar. 2014. <http://www.theplantlist.org>.
Culioli, Gerald, Carole Mathe, and
Paul Archier. Phytochemistry: A Lupane Triterpene from Frankincense.
Elsevier Science Limited. Volume 62. Issue 4 (2003): 537-541. Science
Direct. Web 16 Mar. 2014.
Daly, Douglas C. “Neotropical
Burseraceae.” Kew. Royal Botanical Gardens, 2011. Web. 16 Mar. 2014.
<http://www.kew.org/science/tropamierca/neotropikey/families/Burseraceae.htm>.
Dimmitt, Mark A. “Burseraceae
(torchwood family).” Arizona-Sonora Desert Museum. Association of Zoos &
Aquariums, 2014. Web. 23 Mar. 2014. <www.desertmuseum.org/books/nhsd-burseraceae.php>.
Eggli, Urs. Illustrated Handbook of
Succulent Plants: Dicotyledons. New York: Springer-Verlag Berlin Heidelberg,
2002. Google Books. Web. 24 Mar. 2014. <books.google.com>
Gillman, Edward F. and Dennis G.
Watson. “Burseracea Simaruba: Gumbo-Limbo.” Environmental Horticulture.
2006. Institute of Food and Agricultural Sciences. Web. 23 Mar. 2014.
Harley, Madeline M., Unsook Song, and
Hannah I. Banks. “Pollen Morphology and Systematics of Burseraceae.” Grana.
Volume 44 (2005): 282-299. Taylor & Francis Group. Web. 16 Mar. 2014.
Kane, Dan. “Safou the Butterfruit.” Nourish
the Planet. Worldwatch Institute, 13 Dec. 2010. Web. 23 Mar. 2014.
<blogs.worldwatch.org/nourishtheplanet/safou-the-“butterfruit”/>.
Kubitzki, Klaus. Flowering Plants
Eudicots: Sapindales, Cucurbitales, Myrtaceae. New York: Springer-Verlag
Berlin Heidelberg, 2011. Google Books. Web 24 Mar. 2014.
<books.google.com>.
Maimone, Tom. “Classic Terpene
Syntheses.” Baran Lab. Web. 24 Mar. 2014. <www.scripps.edu/baran/images/grpmtgpdf/maimone-oct-05.pdf>.
“Okoume Fact File.” Arkive.
Wildscreen Conservation, 2013. Web. 23 Mar. 2014.
<www.arkive.org/okoume/aucoumea-klaineana/>.
“Prelude Medicinal Plants Database.” Belspo.
Royal Museum for Central Africa, 2014. Web. 27 Mar. 2014.
<www.africamuseum.be/collections>.
Presl, Berchtold J., “Sapindales.”
Web. 24 Mar. 2014 <www.mobot.org>.
Rosell, Julieta A. and Mark E. Olson.
“Diversification in Species Complexes: Tests of Species Origin and Delimitation
in the Bursera simaruba Clade of
Tropical Trees.” Molecular Phylogenetics and Evolution. Volume 57
(2010): 798-811. Elsevier Science Limited. Web. 23 Mar. 2014.
<w.explorelifeonearth.org/people/Roselletal20105marubacladephylogenty.pdf>.
Salywon, Andrew. “Burseraceae Torchwood
Family.” Journal of the Arizona-Nevada Academy of Science. Volume 32, No. 1
(1999): 29-31. JSTOR. Web. 16 Mar. 2014.
Suhail, Mahmoud M. and Weijuan Wu. “Boswellia sacra suppresses tumor
aggressiveness in cultured human breast cancer cells.” BMC Complementary
& Alternative Medicine. Volume 11. Issue 129 (2011). Biomed Central.
Web. 16 Mar. 2014.
Weeks, Andrea and Beryl B. Simpson.
“Molecular Phylogenetics analysis of Burseraceae.” Molecular Phylogenetics
and Evolution. Volume 42. Issue 1 (2007): 62-79. Science Direct. Web. 16
Mar. 2014.
Woodson, Robert E. and Duncan M.
Porter. “Flora of Panama. Part VI. Family 91. Burseraceae.” Annals of the
Missouri Botanical Garden. Volume 57, No. 1 (1970): 5-27. JSTOR. Web. 16
Mar. 2014.
Yousef, Jehad M. “Identifying Frankincense
Impact on Rats.” Saudi Journal of Biological Sciences. Volume 18. Issue
2 (2011): 1-5 Science Direct. Web. 16 Mar. 2014.