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Canarium
Canarium
Canarium
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For the snail genus, see Canarium (gastropod).

Canarium
Fruiting branch of Canarium harveyi
Scientific classification Edit this classification
Kingdom: Plantae
Clade: Tracheophytes
Clade: Angiosperms
Clade: Eudicots
Clade: Rosids
Order: Sapindales
Family: Burseraceae
Genus: Canarium
L. (1754)[1]
Species

About 120, see text

Synonyms[2]
  • Canariellum Engl. (1896)
  • Canariopsis Miq. (1859)
  • Colophonia Comm. ex Kunth (1824)
  • Lipara Lour. ex Gomes Mach. (1868)
  • Mehenbethene Besler ex Gaertn. (1790)
  • Nanari Adans. (1763)
  • Pimela Lour. (1790)
  • Rumphia L. (1753)
  • Sonzaya Marchand (1867)
  • Strania Noronha (1790), nom. nud.

Canarium is a genus of about 120 species of tropical and subtropical trees, in the family Burseraceae. They grow naturally across tropical Africa, south and southeast Asia, Indochina, Malesia, Australia and western Pacific Islands; including from southern Nigeria east to Madagascar, Mauritius, Sri Lanka and India; from Burma, Malaysia and Thailand through the Malay Peninsula and Vietnam to south China, Taiwan and the Philippines; through Borneo, Indonesia, Timor and New Guinea, through to the Solomon Islands, Vanuatu, New Caledonia, Fiji, Samoa, Tonga and Palau.[3]

Canarium species grow up to large evergreen trees of 40–50 m (130–160 ft) tall, and have alternately arranged, pinnate leaves.[3] They are dioecious, with male and female flowers growing on separate trees.[4]

Species

[edit]

As of January 2024, Plants of the World Online accepts 121 species.[2] The brief species distribution information was sourced from Flora Malesiana,[3] the Flora of China (series), the Australian Tropical Rainforest Plants information system, and Plants of the World Online.

Canarium resiniferum seeds dispersed by hornbills in Pakke Tiger Reserve

Ecology

[edit]

Superb fruit-doves (Ptilinopus superbus) are known to be fond of the fruit of scrub turpentine (C. australianum), which they swallow whole.[5][6]

Many animals feed on the fruit of C. odontophyllum in the wild, such as the red-bellied lemur (Eulemur rubriventer) and the ruffed lemurs (Varecia) of Madagascar's eastern tropical forests. Canarium fruit is also an important part of the diet of the aye-aye (Daubentonia madagascarensis).[7]

Uses

[edit]

Several species have edible nuts, known as galip nut or nangae (C. indicum), pili nut (C. ovatum), or simply canarium nut (C. harveyi and C. indicum). C. indicum are among the most important nut-bearing trees in eastern Indonesia and the Southwest Pacific. C. ovatum is cultivated as a food crop only in the Philippines.[8]

Dammar resin

C. odontophyllum, known commonly as dabai or kembayau, is a species with a nutritious fruit with a creamy taste. It is hard when raw and may be pickled or softened with hot water when prepared.

Canarium album produces a fruit consumed in Vietnam, Thailand (where it is known as nam liap (Thai: หนำเลี้ยบ), samo chin (Thai: สมอจีน) or kana (Thai: กาน้า)) and in China (Chinese: 橄欖) with an appearance of a big olive.

Canarium luzonicum, commonly known as elemi, is a tree native to the Philippines. An oleoresin, which contains Elemicin, is harvested from it.

Canarium strictum produces a resin called black dammar.

References

[edit]
[edit]
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Canarium

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from Grokipedia
Canarium is a of approximately 80 of trees in the family , native to the tropical regions of the , including , , , and the Pacific, with the greatest diversity in the Malesian area. These dioecious canopy trees typically grow to 35–60 meters tall, featuring imparipinnate leaves, paniculate inflorescences, and distinctive drupaceous fruits with three locules and stony endocarps, distinguishing the genus as the largest in the tribe Canarieae. The genus is characterized by its occurrence in primary lowland rainforests and secondary forests up to 1,800 elevation, where species like C. luzonicum and C. ovatum are prominent. Economically, Canarium species are valued for their versatile products: timber known as "kedondong" is used in construction and furniture due to its light brown color and moderate durability; resins, particularly elemi from C. luzonicum, serve in varnishes, perfumes, and medicines; and edible nuts from species such as C. ovatum (pilinuts) and C. indicum (galip nuts) provide nutritious fruits and oils for food, , and . In the , pilinut production reached around 6,000 tons annually as of 2021, while in , galip nuts yield up to 100,000 tonnes per year, highlighting their cultural and commercial significance. Fossil evidence, including mummified fruits from the upper Pleistocene in , underscores Canarium's ancient presence in subtropical to tropical Paleotropics, with species adapting to diverse habitats from moist evergreen forests to areas. Taxonomically, the is subdivided into subgenera such as Canarium, Canariellum, and Africanarium, reflecting its broad morphological variation across regions.

Taxonomy

Etymology and History

The genus Canarium was established by in 1754, drawing directly from the descriptions and illustrations in Georg Eberhard Rumphius' Herbarium Amboinense (1741–1750), a seminal work documenting the flora of the Ambon region in the Moluccas. Rumphius provided the first detailed European accounts of Canarium species, recognizing 12 variants based on local observations in the Moluccas, where the trees were valued for their and nuts. Linnaeus formalized the genus in his Herbarium Amboinense (p. 9), with subsequent species like C. indicum L. published in Amoenitates Academicae 4: 143 in 1759, incorporating Rumphius' material as the type basis. The name Canarium derives from the Malay term "kanari" and the related Moluccan "kenari," vernacular names used for these resin-producing trees in their native range. Early taxonomic work by Linnaeus and contemporaries occasionally conflated Canarium with other genera like Boswellia due to shared resinous exudates and woody habits, though distinctions emerged through and characters. Taxonomic recognition of Canarium evolved from Rumphius' regional accounts in the to broader systematic treatments in the . P.W. Leenhouts' comprehensive revision in for the Malaysian region consolidated descriptions into approximately 75 , emphasizing geographic patterns and reducing synonyms from earlier scattered publications. Subsequent regional floras and phylogenetic studies have expanded the count to around 120 across tropical , , and , reflecting increased collections and molecular insights into its diversity.

Classification and Synonyms

The genus Canarium belongs to the kingdom Plantae, phylum Tracheophyta, class Magnoliopsida, order Sapindales, family Burseraceae, subfamily Canarioideae. This placement reflects its position among tropical and subtropical trees characterized by resinous properties and compound leaves typical of the Burseraceae. Several generic synonyms have been proposed for Canarium, including Canariellum Warb., Canariopsis Seem., Hemistemon Engl., and the misapplied Premna L., while Rottlera Lour. has been used for certain species now included within the genus. These synonyms arose from historical taxonomic treatments that separated groups based on minor morphological variations, but subsequent revisions consolidated them under Canarium. Subgeneric divisions within Canarium are informal and primarily based on leaf and fruit morphology, such as distinctions between sections featuring simple leaves versus compound ones, or variations in fruit wing structure. Key revisions establishing these groupings were conducted by Leenhouts in the 1950s, who recognized about 75 species across informal sections like Sect. Canarium and Sect. Pimela, and by Ding Hou in his 1978 treatment of in Flora Malesiana, which refined classifications for Malesian species emphasizing and resin canal differences. The genus is further subdivided into three subgenera: subg. Canarium (widespread from to the Pacific), subg. Canariellum (Engl.) Leenh. (restricted to eastern , New Caledonia, and adjacent islands), and subg. Africanarium (Leenh.) Leenh. (monotypic, confined to western ). The for the Canarium is Canarium indicum L., based on Linnaeus's 1759 drawing from Rumphius's illustrations of resin-producing trees in Ambon.

Description

Morphological Features

Canarium are typically large trees reaching heights of 20–50 meters, with straight boles that can attain diameters of 1–2 meters in mature individuals; buttresses are common, particularly in larger , providing structural support in environments. The leaves are alternate and imparipinnate, consisting of 5–21 leathery leaflets arranged spirally along a rachis measuring 10–30 cm in length; the leaflets are oblique at the base, entire to dentate at the margins, thick and acuminate at the apex, and release an aromatic scent when crushed due to the presence of glands. Flowers are dioecious and unisexual, measuring 3–13 mm in diameter, and borne in axillary or terminal panicles up to 34 cm long; they are trimerous with a synsepalous calyx of three sepals, three distinct valvate petals that are creamy to yellowish, male flowers featuring six stamens in two whorls surrounding a 6-lobed disk, and female flowers with a 3-locular comprising three carpels. Fruits are indehiscent compound drupes, to ovoid and 1–5 cm long, with a thin exocarp, fleshy mesocarp, and a bony 3-celled containing typically one developed (nut); they mature from green to blue-black or dark brown, often with a resinous exocarp. The bark is rough and fissured, ranging from smooth to scaly or lenticellate, with colors varying from grayish to light yellow-brown; wounds in the bark exude an oleo- that is yellowish and aromatic, with schizogenous resin canals present throughout vascular tissues; in species such as C. luzonicum, this resin is known as elemi.

Growth and Reproduction

Canarium species exhibit slow to moderate growth during their juvenile phase, with transplanted seedlings initially advancing at a reduced pace before accelerating. For instance, in Canarium ovatum, juvenile trees reach heights of 2 meters or more within 3–4 years, while C. indicum grows 0.6–2 meters in the first year, followed by rapid annual increments of 2.5–3 meters for the subsequent 5–6 years. Maturity, marked by the onset of fruit production, typically occurs 5–8 years after planting for seedlings, with full productive capacity achieved around 10–15 years in species like C. ovatum. In undisturbed forest conditions, individuals can attain lifespans exceeding 100 years, contributing to long-term canopy dominance. Most Canarium species are dioecious, necessitating proximity between trees for successful seed set, as unisexual flowers occur on separate individuals. Flowering is generally seasonal and aligns with drier periods, featuring inflorescences that support male flowers producing abundant ; examples include C. ovatum blooming from March to May and C. strictum initiating in late March. Fruit development follows , with drupes maturing 3–6 months later, as observed in C. ovatum and C. strictum, where maturation spans from late March to June. Seeds maintain viability for short periods, often less than 60 days without storage, though some treatments extend this to 1–2 years under cool, dry conditions. Propagation occurs mainly through seeds, which face challenges from and exhibit rates of 20–50% even with pretreatments like or soaking, as seen in C. strictum achieving up to 48% success. For C. ovatum, takes 30–60 days at 25–30°C following , reaching 70–80% under optimal conditions. Vegetative methods, such as marcotting or cuttings, are infrequently used but viable in cultivation to bypass seed limitations. Phenological patterns vary regionally, with equatorial populations showing more protracted or year-round cycles compared to seasonal expressions in monsoonal areas. In the (equatorial), C. ovatum displays frequent flowering and prolonged fruit ripening, while in monsoonal of , C. strictum follows a strict March–June sequence tied to post-monsoon drying. Similarly, C. indicum in the (equatorial) fruits August–October, contrasting with October–January in Vanuatu's variable tropics.

Distribution and Habitat

Geographic Range

The genus Canarium is native to the paleotropics, with a broad distribution spanning tropical , , , and the Pacific Islands. In , species occur from (e.g., , ) through central regions (e.g., Democratic Republic of Congo) to (e.g., , ), including high on , where approximately 33 species are recognized, most of them narrow endemics. This represents a significant portion of the genus's diversity in the region. In contrast, the region hosts the majority of Canarium species, with the greatest diversity in (e.g., , , , ) and extending into (e.g., , ). Insular distributions show pronounced , particularly in the Pacific, where species are recorded on islands such as , , , and , the latter featuring multiple endemic species adapted to local conditions. This continental-insular pattern underscores the genus's adaptation to diverse tropical environments, with greater species richness in the compared to . Fossil evidence supports a paleotropical origin for Canarium, with records of fruits and flowers dating to the in , such as well-preserved specimens from Province, , indicating an ancient presence in the region. These fossils suggest the genus's distribution has remained centered in the tropics since at least the middle . Introductions outside the native range are limited; for instance, C. ovatum has been cultivated in since 1922 for its edible nuts and trialed in , though it shows limited tolerance to cooler conditions there.

Environmental Preferences

Canarium species are adapted to tropical lowland and montane environments, typically occurring from to elevations of 0–1,500 m, though some like C. indicum extend to 1,850 m in exceptional cases. They flourish in climates with mean annual temperatures of 23–28°C, mean maxima of 27–32°C, and minima of 15–24°C, requiring frost-free conditions. Annual rainfall ranges from 1,800–4,000 mm, with optimal growth in 2,500–3,000 mm evenly distributed or with a short of less than 1–3 months; many species exhibit tolerance to brief seasonal droughts of up to 3–4 months. Soil preferences for the emphasize well-drained, fertile loams or sandy clay loams with moderate to high fertility and neutral levels of 5.5–7.4; they perform on volcanic, alluvial, or lateritic substrates but show poor tolerance to waterlogging, shallow, infertile, or saline conditions. While capable of growth in slightly impeded drainage for short periods, prolonged saturation leads to root issues, and the deep system aids stability in these friable soils. In terms of habitat, Canarium trees inhabit primary rainforests, secondary s, and forest edges, often in old garden sites near settlements; they are light-demanding as mature individuals in canopy gaps but shade-tolerant as saplings, enduring 25–70% shade initially before requiring reduced shading after 3–4 years. Adaptations include short-term resistance via physiological mechanisms and deep rooting, alongside production of that may aid in during dry spells, though the volatile nature of bark renders them sensitive to . Some display morphological plasticity, such as reduced size at higher elevations in response to cooler temperatures and increased wind exposure.

Diversity

Species Count and Distribution

The genus Canarium encompasses approximately 121 accepted species as of 2025, based on the authoritative database ; however, historical estimates have ranged from 75 to 150 owing to persistent taxonomic revisions and varying criteria for species delimitation. Species richness peaks in Malesia, where roughly 50 species occur, particularly in (approximately 33 species) and the (9–10 species), reflecting the region's extensive tropical rainforests and geological history as a . In , diversity is lower at about 35 species, with a notable concentration of 33 species in alone, many of which are confined to the island's humid forests. The Pacific islands support around 20 species, concentrated in , while has comparatively few, with 2–3 species primarily in northern rainforests. Endemism is pronounced on oceanic islands, where isolation fosters speciation; for instance, C. whitei is an endemic species in , contrasting with more widespread continental species that span multiple regions like and . Continental distributions often exhibit broader ranges, linking African and Asian populations through ancient dispersal corridors. Taxonomic challenges arise from hybridization events and morphological similarities, which have led to frequent synonymy and debates over species boundaries; recent molecular phylogenetic studies, including genomic analyses, have clarified major clades and revealed admixture in regions like , aiding in resolving these ambiguities.

Notable Species

, commonly known as the pili nut, is endemic to the , with its center of diversity in regions such as Bicol, , and Islands. This species is a large that can reach heights of up to 20 meters, featuring a buttressed trunk and dense crown suitable for . Its large, edible nuts are a significant resource for the , often processed into snacks, oils, and due to their rich, buttery kernel. Widely cultivated beyond its native range, including in , the supports both commercial production and local livelihoods. However, historical has raised concerns, though its IUCN status was uplisted from Vulnerable to Least Concern in following improved assessments. Canarium luzonicum, referred to as elemi or elemi, is a species valued primarily for its , a soft, pale yellow to greenish substance with a balsamic used in varnishes, adhesives, and perfumes. The tree grows to about 30 meters tall in lowland rainforests and primary forests at low to medium elevations, with aromatic leaves that contribute to its resin's distinctive pine-lemon scent. Harvesting involves making incisions in the bark from to , yielding a weekly collection of gum. Its IUCN status improved from Vulnerable to Near Threatened in 2020, reflecting ongoing pressures but no immediate risk. Canarium indicum, the galip nut, is native to eastern , including , , and , where it thrives in rainforests, secondary forests, and old garden sites. This mainly dioecious evergreen tree typically reaches 25 meters, occasionally up to 40 meters, with a dense crown and twisted stem featuring buttresses. Its edible kernel is notably high in fat, making it a and export commodity, while the species integrates into traditional systems as one of the oldest cultivated tree crops in the region. Not formally assessed by IUCN, it faces no major conservation threats but benefits from practices. Canarium odontophyllum, known as dabai or , is indigenous to , particularly in and , where it grows in mixed dipterocarp forests up to 1,000 meters elevation. The tree produces oval drupes with a purple-black and white pulp that are eaten fresh after light boiling or salting, prized for their olive-like flavor. Beyond nutrition, the fruit and leaves exhibit medicinal properties, including , antidiabetic, and effects, supported by high levels of , minerals, and bioactive compounds. It remains unassessed by IUCN, with potential for greater utilization to support local economies without significant conservation issues. Canarium schweinfurthii, or African elemi, is a large tree distributed across tropical , including East African regions like and , in lowland and submontane rainforests. Capable of reaching 50 meters with a long, clean bole and upper-canopy crown, it serves as a key source of timber—known as aiele—with interlocked grain yielding attractive figured wood for and furniture—and elemi for medicinal and industrial applications. The is rated Least Concern by IUCN, indicating stable populations despite localized harvesting pressures.

Ecology

Pollination and Seed Dispersal

Pollination in the genus Canarium is often entomophilous, facilitated by nectar rewards in small, unisexual flowers arranged in terminal inflorescences. Insect visitors include bees such as Apis dorsata and carpenter bees (Xylocopa spp.), which are the most frequent pollinators, along with butterflies, wasps, flies, and ants in Asian species like C. strictum. The dioecious nature of most Canarium species, with separate male and female trees, precludes self-pollination and relies on cross-pollination for genetic exchange. Some anemophily occurs in exposed habitats, where wind aids pollen transfer between synchronized flowering trees, particularly in C. strictum. Pollination success varies regionally; for instance, open pollination in C. strictum yields about 52% fruit set, while hand cross-pollination achieves up to 91%, with lower rates reported in fragmented forests due to reduced pollinator visitation. Seed dispersal in Canarium is predominantly zoocorous, with fleshy drupes attracting frugivores that consume the and excrete intact seeds. Primary dispersers include large birds such as hornbills (Buceros spp., Aceros spp.) in Asian forests, which swallow fruits whole and deposit seeds at distances averaging around 250 m. In and Australian rainforests, cassowaries (Casuarius casuarius) effectively disperse medium-sized drupes of species like C. muelleri, often retaining 1–2 seeds per dropping. Mammalian frugivores, such as lemurs (Varecia variegata, Eulemur spp.) in , transport seeds up to 624 m, with average distances around 100 m for various Canarium species. Dispersal distances typically range from 50–500 m, promoting across habitats. Secondary dispersal often involves , such as squirrels and rats, which cache or move seeds short distances after primary deposition by birds or mammals. For C. euphyllum in , ground-dwelling mammals like squirrels predating fallen fruits contribute to this process. Unconsumed fruits frequently fall beneath parent trees and germinate locally, though this limits dispersal and increases competition. In fragmented landscapes, reduced abundance can lower dispersal efficiency, leading to clustered seed rain and impaired .

Interactions with Wildlife

Canarium species engage in various trophic interactions with wildlife, particularly through herbivory on foliage and resin, which serves as a chemical defense against certain insect pests. Leaves of Canarium trees are occasionally browsed by primates and insects, though the resin exuded from the bark and wounds acts as a deterrent to some herbivores and pathogens. For instance, the essential oil derived from Canarium schweinfurthii exhibits strong anti-termite activity, inhibiting feeding and survival of subterranean termites (Rhinotermes spp.) at low concentrations, highlighting its role in reducing wood-boring damage in natural settings. Seeds of Canarium are subject to predation by and other mammals, which can significantly influence recruitment in forest understories. In moist evergreen forests of , seeds of Canarium euphyllum are primarily predated by rare mammals such as the Indochinese ground squirrel (Menetes berdmorei) and giant long-tailed rat (Leopoldamys sabanus), with removal rates highest near conspecific feeding trees where dispersal agents like hornbills deposit them. In Madagascar's rainforests, including Eliurus and Nesomys spp. act as secondary dispersers but predates up to 19% of removed Canarium seeds, often caching them before consumption, which can limit germination success. While primates like aye-ayes (Daubentonia madagascariensis) consume some seeds opportunistically as part of their omnivorous diet, direct predation on Canarium remains incidental compared to their primary insectivory. Symbiotic relationships further integrate Canarium into forest ecosystems, notably through mycorrhizal associations that enhance nutrient uptake in nutrient-poor tropical soils. Canarium schweinfurthii forms arbuscular mycorrhizae (AM) with root colonization rates of 51–75%, facilitating phosphorus and nitrogen acquisition in the infertile, sandy soils of Central African rainforests. These associations are widespread in the Burseraceae family, supporting tree growth in low-fertility habitats where AM fungi extend the root system's reach for scarce resources. Although potential mutualisms with ants via extrafloral nectaries have been hypothesized for some tropical trees, no verified ant-plant interactions specific to Canarium have been documented. As in tropical forests, Canarium trees provide critical services by forming expansive canopies that offer and sites for epiphytes, birds, and arboreal mammals. In , the genus is recognized as a large-seeded keystone taxon in rainforests, where its fruits support frugivorous lemurs (e.g., Varecia variegata and Eulemur spp.) that disperse seeds over distances up to 624 m, maintaining forest composition and . The resin's properties also contribute indirectly to by inhibiting microbial proliferation in surrounding soils and . Canarium exhibits low invasive potential outside native ranges, but in deforested areas, increased accessibility may heighten browsing pressure from generalist herbivores, potentially slowing regeneration without natural canopy protection.

Uses

Edible Products

The nuts of several Canarium are valued for their high nutritional content and versatility in culinary applications. The pili nut (C. ovatum), native to the , is commonly roasted for direct consumption or incorporated into confections such as brittle and pralines due to its creamy texture and rich flavor. These nuts contain approximately 70% oil, primarily composed of monounsaturated fats like , along with significant levels of magnesium (302 mg per 100 g) and essential . Similarly, galip nuts (C. indicum), prevalent in and the , are eaten raw, roasted, or smoked, providing about 14% crude protein, 50-76% oil, and essential minerals including 81 mg/kg iron and 50 mg/kg zinc per kernel. The fruits of Canarium species also serve as edible resources in various Southeast Asian cuisines. Dabai fruit (C. odontophyllum), from Borneo, is traditionally boiled with salt to soften its leathery skin, revealing a sweet-sour pulp rich in vitamins A and C, as well as healthy fats that contribute to its 339 kcal energy per 100 g serving. In contrast, the fruits of C. album, known as Chinese olive, are pickled, stir-fried, or used in Vietnamese and Chinese dishes for their tangy profile, offering essential , unsaturated fatty acids, and vitamins that support activity. Extracting kernels from Canarium nuts presents challenges due to their hard shells, often requiring manual cracking with stones or modern methods like soaking in hot water followed by for 2-3 days to facilitate depulping and shell separation. The extracted kernel oil, suitable for cooking, exhibits a favorable fatty acid profile with high content, while traditional processing in some Pacific cultures includes or to enhance and flavor. In indigenous communities of , Canarium nuts have been a dietary staple for over 6,000 years, providing a key source of fats and proteins during seasonal scarcities and holding cultural importance in ceremonies and systems. Pili nuts from the support a growing export market, with the accounting for about 84% of national production and facilitating shipments to and .

Resin and Timber

The resin extracted from various Canarium species serves as a key non-edible product, particularly elemi from C. luzonicum, which is tapped from trees in the and used in varnishes for its ability to enhance toughness and elasticity, as well as in for its balsamic aroma. This soft, pale yellow , which hardens upon exposure to air, yields approximately 1–5 kg per mature tree annually through traditional tapping methods involving horizontal incisions about 2 cm high and 30 cm long on trunks of 20–60 cm diameter, with sites rechipped every 2–7 days to maintain flow. Another notable is black dammar from C. strictum, a clear amber-colored employed in lacquers and varnishes due to its and adhesive qualities. The resins exhibit aromatic and sticky properties characteristic of oleoresins, with elemi featuring a spicy, bitter and balsamic that make it suitable for industrial applications. Chemically, elemi comprises about 25–30% , dominated by (56%) and α-phellandrene (18%), alongside resenes (56–61%), resin acids (15–18%), and minor like elemol and , contributing to its volatility and scent profile. Black dammar shares similar components but is distinguished by its harder texture and use in spirit varnishes. techniques for both emphasize shallow incisions to avoid the tree, allowing repeated harvests over decades without immediate mortality. Timber from Canarium species provides durable heartwood valued for and furniture, featuring a straight to interlocked grain and fine texture that machines well. The wood density ranges from 500–700 kg/m³ at 12–15% moisture content, offering moderate strength suitable for indoor framing, , and . C. schweinfurthii, in particular, is preferred for these purposes due to its pinkish-brown heartwood, which is used in veneers, parquetry , and furniture components, though it requires treatment against and decay. Beyond resin and timber, bark from certain Canarium yields dyes, such as extracts used traditionally for coloring textiles, while leaves are employed in folk medicine for their effects, often as decoctions to alleviate and respiratory issues. Commercially, elemi from the supported exports of 200–300 tons annually as of the late 1990s, primarily to and for and industries, with free-on-board prices fluctuating between US$1.67–4.50/kg in the 1990s. Sustainable harvesting guidelines emphasize non-girdling taps and rotational incisions to ensure tree longevity up to 50–60 years, as promoted by regional institutes to prevent overexploitation.

Conservation

Threats

Canarium species face multiple anthropogenic and environmental threats that jeopardize their populations across and the Pacific. loss is a primary concern, driven by for agricultural expansion, including oil palm plantations, and commercial logging. In the , native forest habitats essential for their growth are fragmented and destroyed by anthropogenic activities. Overexploitation exacerbates these pressures through unsustainable harvesting practices. tapping, often involving and excessive incisions, leads to high adult tree mortality and reduced regeneration in species like Canarium strictum, where populations have declined by approximately 20% between 2003 and 2013 due to intensive collection for medicinal and industrial uses. Similarly, nut harvesting for products in C. ovatum and related species outpaces natural replenishment in wild stands, further hindering seedling establishment and long-term viability. for high-value timber also targets mature Canarium trees, compounding regeneration challenges across the genus. Climate change poses additional risks by altering precipitation patterns and increasing temperature variability, which disrupt flowering and fruiting cycles critical for Canarium reproduction. Island-endemic species, such as those in the Indonesian archipelago, are especially susceptible to sea-level rise, which threatens coastal habitats and exacerbates erosion in low-lying areas. Invasive species and pests further compound vulnerabilities, particularly in disturbed secondary forests. Competitive weeds can outcompete Canarium seedlings for resources, while pests such as borers and psyllids (Pseudophacopteron calilungae) damage cultivated and wild trees, leading to defoliation and reduced yields in species like C. ovatum and C. indicum. In regions like Papua New Guinea, invasive insects including shield bugs (Amblypelta cocophaga) and mealybugs (Coccus spp.) have been recorded attacking fruits and stems, amplifying losses in already stressed populations.

Status and Efforts

The conservation status of most Canarium species remains poorly documented, with a significant portion classified as on the due to limited assessments across the genus's approximately 100 species. Among the assessed taxa, the majority are categorized as Least Concern, reflecting their relatively wide distributions in tropical forests, though approximately 10% are threatened, including several such as Canarium kipella in and Canarium madagascariense in . Canarium paniculatum in is also assessed as Endangered, primarily due to habitat loss in lowland rainforests. Several Canarium species occur within protected areas that contribute to their . For instance, C. madagascariense is found in Madagascar's , a encompassing landscapes and dry forests where the species persists along watercourses. In , Canarium species are represented in Bornean reserves that safeguard montane and lowland ecosystems supporting diverse taxa. These protected zones help mitigate localized pressures, though coverage remains fragmented across the genus's range in , , and the Pacific. Ongoing conservation efforts emphasize community-based initiatives and sustainable management. In the , programs promote C. ovatum (pili nut) cultivation among indigenous communities, integrating the tree into systems to enhance livelihoods while preserving ; these efforts have supported on degraded lands with propagation success rates of 85-90% via techniques. Resin harvesting from species like C. luzonicum benefits from certification schemes promoting sustainable tapping practices, including organic standards that ensure minimal environmental impact and for producers in . Ex-situ conservation includes collections in botanic gardens, with such as C. kipella represented in at least four global institutions, as documented by Botanic Gardens Conservation International (BGCI); notable repositories include those at and , which hold specimens for research and propagation. Research priorities focus on to bolster resilience against and , with studies advocating for molecular analyses of wild populations. Reforestation trials in mixed-species plantations highlight the genus's potential in restoration but underscore needs for site-specific . Policy frameworks provide additional safeguards: no Canarium species are listed under , but national protections apply, such as Indonesia's regulations on timber-yielding taxa like C. odontophyllum and Malaysia's reserve designations for commercial species.

References

  1. https://prosea.prota4u.org/view.aspx?id=4008
  2. https://pmc.ncbi.nlm.nih.gov/articles/PMC9646933/
  3. https://www.sciencedirect.com/topics/agricultural-and-biological-sciences/canarium
  4. https://sdiopr.s3.ap-south-1.amazonaws.com/2023/Feb/2023_AJAEES_95888/Ms_AJAEES_95888.pdf
  5. https://powo.science.kew.org/taxon/urn:lsid:ipni.org:names:5127-1
  6. https://www.nparks.gov.sg/florafaunaweb/flora/3/6/3659
  7. https://repository.naturalis.nl/pub/525660
  8. https://www.botanikks.com/plants/burseraceae/712372/1
  9. https://powo.science.kew.org/taxon/urn:lsid:ipni.org:names:77126617-1
  10. https://www.researchgate.net/publication/226794319_Burseraceae
  11. https://repository.naturalis.nl/pub/532496/FM1S1974008001013.pdf
  12. https://www.researchgate.net/publication/351339148_Morphological_and_quality_characteristics_of_genus_of_Canarium_L_A_review
  13. https://sciencepress.mnhn.fr/sites/default/files/articles/hd/a2015n2a2-pdfa.pdf
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