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Internal ID UUID64400de4889e8124398059
Scientific name Bruguiera parviflora
Authority Wight & Arn. ex W.Griffith
First published in Trans. Med. Soc. Calcutta 8: 10 (1836)

Ethnobotanical Use Top

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General Uses Top

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Common products:
- Timber (heartwood and sapwood) used for structural beams, poles, and light‑duty furniture.
- Fuelwood and charcoal; the wood’s low moisture and high calorific value (~19 MJ kg⁻¹) make it suitable for direct combustion or carbonization.
- Pulp for paper; wood chips are processed by the kraft method to produce paper‑grade pulp.
- Tannin extracts from bark and leaves; hydrolyzable gallotannins (≈20–30 % of dry weight) are used in leather tanning.

Industrial and craft applications:
- Particleboard and fiberboard; the wood’s moderate density and dimensional stability allow production of low‑load boards for furniture and interior panels.
- Veneer and plywood; thin slices are used for interior finishing and decorative surfacing.
- Handicraft items (e.g., small carvings, tool handles) that exploit the wood’s fine grain.
- Light‑construction elements such as scaffolding poles and temporary shelters.

Colorants and tanning:
- Natural brown dyes; aqueous extracts of bark provide brown coloration on protein fibers (silk, wool).
- Leather tanning; hydrolyzable tannins from the bark impart astringency and durability to tanned hides.

Wood and fiber:
- Structural timber with a basic density of 0.70–0.80 g cm⁻³ and bending strength of ≈70 MPa, suitable for joists, flooring sub‑structures, and interior paneling.
- Wood chips for kraft pulp; the species’ lignin (~30 %) and cellulose (~45 %) ratios support a pulp yield of ~45 % on a dry‑basis.

Properties relevant to use:
- High extractive content contributes to natural decay resistance.
- Low equilibrium moisture content (≈10–12 % at air‑dry) improves fuel performance.
- Tannin class (hydrolyzable gallotannins) and concentration support leather‑tanning applications.
- Calorific value and moderate strength enable use as construction timber and charcoal feedstock.

Standards and regulation:
- FAO guidelines for sustainable mangrove timber (FAO, 2016) provide harvesting and management recommendations.
- ISO 13061 governs charcoal quality (moisture, calorific value).
- ISO 2470 specifies pulp kappa‑number determination for paper manufacturing.
- National timber grading standards (e.g., Myanmar Timber Grading Manual, 2018) classify sawn timber for trade.
- Analytical protocols for tannin quantification (e.g., Folin–Ciocalteu assay) are accepted under national chemical‑testing regulations.

Sustainability and sourcing:
- Regional mangrove assessments indicate local population declines due to habitat conversion and over‑harvest for fuelwood.
- Sustainable harvesting cycles of 10–15 years and community‑based management are promoted to reduce pressure.
- Limited FSC certification exists for mangrove timber in selected jurisdictions.
- Restoration programs incorporate artificial regeneration of B. parviflora to replenish stocks.

Scientific and model‑organism use:
- Employed in physiological and transcriptomic studies of mangrove stress tolerance; RNA‑Seq datasets are deposited in NCBI SRA.
- Seed banks and germplasm collections maintained by mangrove research institutes facilitate comparative genomics within Rhizophoraceae.
- Used to develop standardized seedling establishment protocols for mangrove reforestation trials.

Synonyms Top

Scientific name Authority First published in
Kanilia parviflora Blume Mus. Bot. 1: 140 (1850)
Rhizophora parviflora Roxb. Fl. Ind. 2: 461 (1824)
Rhizophora pauciflora Griff. Not. Pl. Asiat. 4: 664 (1854)
Bruguiera ritchiei Merr. Philipp. Gov. Lab. Bur. Bull. 6: 11 (1903)

Common names Top

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Language Common/alternative name
English smallflower bruguiera
Bengali বকুল কাঁকড়া
Bengali বকুল চাঁপা
Indonesian lenggadai
Malay pokok lenggadai
Malay lenggadai
Thai ถั่วดำ

Subspecies (abbr. subsp./ssp.) Top

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Varieties (abbr. var.) Top

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Subvarieties (abbr. subvar.) Top

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Forms (abbr. f.) Top

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Germination/Propagation Top

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Distribution (via POWO/KEW) Top

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Links to other databases Top

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Database ID/link to page
World Flora Online wfo-0000572758
USDA Plants BRPA15
KEW urn:lsid:ipni.org:names:719542-1
The Plant List kew-2684048
Open Tree Of Life 867713
Observations.org 506630
NCBI Taxonomy 106618
IUCN Red List 178821
IPNI 719540-1
iNaturalist 189948
GBIF 5384934
Freebase /m/011jjhn_
EOL 487631
Elurikkus 595868
USDA GRIN 8005
Wikipedia Bruguiera_parviflora

Genomes (via NCBI) Top

Below is displayed the reference genome only!
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Accession Assembly
Name Level Submitter Released Coverage Size
GCA_019804595.1 ASM1980459v1 Chromosome National Science and Technology Development Agency 2021-08-31 105 200.64 Mb

Scientific Literature Top

Below are displayed the latest 15 articles published in PMC (PubMed Central®) and other sources (DOI number only)!
If you wish to see all the related articles click here.
Title Authors Publication Released IDs
Detection of a bibenzyl core scaffold in 28 common mangrove and associate species of the Indian Sundarbans: potential signature molecule for mangrove salinity stress acclimation Sarkar B, Kotal HN, Giri CK, Mandal A, Hudait N, Madhu NR, Saha S, Basak SK, Sengupta J, Ray K Front Plant Sci 16-Jan-2024
PMCID:PMC10824835
doi:10.3389/fpls.2023.1291805
PMID:38293624
Characterization of the complete chloroplast genome of Carallia brachiata (Lour.) Merr. (Rhizophoraceae) Zhou Y, She J, Jin C, Zhu X, Xiao F, Zhao J Mitochondrial DNA B Resour 16-Aug-2023
PMCID:PMC10435000
doi:10.1080/23802359.2023.2238935
PMID:37600503
Photosynthetic efficiency and transcriptome analysis of Dunaliella salina under hypersaline: a retrograde signaling mechanism in the chloroplast Ramachandran P, Pandey NK, Yadav RM, Suresh P, Kumar A, Subramanyam R Front Plant Sci 21-Jun-2023
PMCID:PMC10322210
doi:10.3389/fpls.2023.1192258
PMID:37416885
RNA-sequencing transcriptome analysis of Avicennia marina (Forsk.) Vierh. leaf epidermis defines tissue-specific transcriptional response to salinity treatment Li H, Lv CT, Li YT, Gao GY, Meng YF, You YL, Tian Q, Liang KQ, Chen Y, Chen H, Xia C, Rui XY, Zheng HL, Wei MY Sci Rep 10-May-2023
PMCID:PMC10172313
doi:10.1038/s41598-023-34095-x
PMID:37165000
Insights into Bacterial Communities and Diversity of Mangrove Forest Soils along the Upper Gulf of Thailand in Response to Environmental Factors Nimnoi P, Pongsilp N Biology (Basel) 08-Dec-2022
PMCID:PMC9775068
doi:10.3390/biology11121787
PMID:36552296
Characterization of the complete chloroplast genome of Carallia diplopetala (Rhizophoraceae) Wang R, Liao N, Liu X, Qin Y, Xiao Y, Wang Y, Huang R Mitochondrial DNA B Resour 27-Oct-2022
PMCID:PMC9621227
doi:10.1080/23802359.2022.2135398
PMID:36325279
Antimicrobial potentials of natural products against multidrug resistance pathogens: a comprehensive review Elmaidomy AH, Shady NH, Abdeljawad KM, Elzamkan MB, Helmy HH, Tarshan EA, Adly AN, Hussien YH, Sayed NG, Zayed A, Abdelmohsen UR RSC Adv 13-Oct-2022
PMCID:PMC9558262
doi:10.1039/d2ra04884a
PMID:36320761
Assessment of the Genetic Diversity and Population Structure of Rhizophora apiculata Blume (Rhizophoraceae) in Thailand Ruang-areerate P, Naktang C, Kongkachana W, Sangsrakru D, Narong N, Maknual C, Pravinvongvuthi T, Promchoo W, Yamprasai S, Tangphatsornruang S, Pootakham W Biology (Basel) 01-Oct-2022
PMCID:PMC9598538
doi:10.3390/biology11101449
PMID:36290353
Metabolic Pathway of Natural Antioxidants, Antioxidant Enzymes and ROS Providence Huchzermeyer B, Menghani E, Khardia P, Shilu A Antioxidants (Basel) 11-Apr-2022
PMCID:PMC9025363
doi:10.3390/antiox11040761
PMID:35453446
Dataset of physico-chemical water parameters, phytoplankton, flora and fauna in mangrove ecosystem at Sungai Kertih, Terengganu, Malaysia Nor SM, Jaafar M, Jaafar NM, Redzuan NS, Omar WB, Deraman MY, Azli SN, Shehrom NA, Mahyudin ', Bahari NA, Zulkafli NN, Jaafar NF, Ma'ad SN, Zamri MI, Amirudin A, Abdullah NA, Zakaria N Data Brief 26-Mar-2022
PMCID:PMC9011031
doi:10.1016/j.dib.2022.108096
PMID:35434213
Comparative Analysis and Phylogenetic Relationships of Ceriops Species (Rhizophoraceae) and Avicennia lanata (Acanthaceae): Insight into the Chloroplast Genome Evolution between Middle and Seaward Zones of Mangrove Forests Ruang-areerate P, Yoocha T, Kongkachana W, Phetchawang P, Maknual C, Meepol W, Jiumjamrassil D, Pootakham W, Tangphatsornruang S Biology (Basel) 28-Feb-2022
PMCID:PMC8945693
doi:10.3390/biology11030383
PMID:35336757
De Novo Reference Assembly of the Upriver Orange Mangrove (Bruguiera sexangula) Genome Pootakham W, Naktang C, Sonthirod C, Kongkachana W, Yoocha T, Jomchai N, Maknual C, Chumriang P, Pravinvongvuthi T, Tangphatsornruang S Genome Biol Evol 11-Feb-2022
PMCID:PMC8872974
doi:10.1093/gbe/evac025
PMID:35148390
Improvement of Selected Morphological, Physiological, and Biochemical Parameters of Roselle (Hibiscus sabdariffa L.) Grown under Different Salinity Levels Using Potassium Silicate and Aloe saponaria Extract Abou-Sreea AI, Roby MH, Mahdy HA, Abdou NM, El-Tahan AM, El-Saadony MT, El-Tarabily KA, El-Saadony FM Plants (Basel) 11-Feb-2022
PMCID:PMC8879578
doi:10.3390/plants11040497
PMID:35214829
A de novo reference assembly of the yellow mangrove Ceriops zippeliana genome Pootakham W, Sonthirod C, Naktang C, Kongkachana W, U-thoomporn S, Phetchawang P, Maknual C, Jiumjamrassil D, Pravinvongvuthi T, Tangphatsornruang S G3 (Bethesda) 02-Feb-2022
PMCID:PMC8982413
doi:10.1093/g3journal/jkac025
PMID:35106563
Metabarcoding of Fish Larvae in the Merbok River Reveals Species Diversity and Distribution Along its Mangrove Environment Alshari NF, Ahmad SZ, Azlan A, Lee YH, Azzam G, Nor SA Zool Stud 22-Dec-2021
PMCID:PMC9169113
doi:10.6620/ZS.2021.60-76
PMID:35774258

Phytochemical Profile Top

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Below are displayed the proven (via scientific papers) natural compounds!
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Name PubChem ID Canonical SMILES MW Found in Proof
> Lipids and lipid-like molecules / Prenol lipids / Triterpenoids
((1R,3aR,5aR,5bR,7aR,9S,11aR,11bR,13aR,13bR)-3a,5a,5b,8,8,11a-hexamethyl-1-prop-1-en-2-yl-1,2,3,4,5,6,7,7a,9,10,11,11b,12,13,13a,13b-hexadecahydrocyclopenta(a)chrysen-9-yl) (E)-3-(3,4-dihydroxyphenyl)prop-2-enoate 12149208 Click to see 588.90 unknown https://doi.org/10.1248/CPB.53.95
(3a,5a,5b,8,8,11a-Hexamethyl-1-prop-1-en-2-yl-1,2,3,4,5,6,7,7a,9,10,11,11b,12,13,13a,13b-hexadecahydrocyclopenta[a]chrysen-9-yl) 3-(3,4-dihydroxyphenyl)prop-2-enoate 73101157 Click to see 588.90 unknown https://doi.org/10.1248/CPB.53.95
(3a,5a,5b,8,8,11a-Hexamethyl-1-prop-1-en-2-yl-1,2,3,4,5,6,7,7a,9,10,11,11b,12,13,13a,13b-hexadecahydrocyclopenta[a]chrysen-9-yl) 3-(4-hydroxyphenyl)prop-2-enoate 73107757 Click to see 572.90 unknown https://doi.org/10.1248/CPB.53.95
[(1R,3aR,5aR,5bR,7aR,9R,11aS,11bR,13aR,13bS)-3a,5a,5b,8,8,11a-hexamethyl-1-prop-1-en-2-yl-1,2,3,4,5,6,7,7a,9,10,11,11b,12,13,13a,13b-hexadecahydrocyclopenta[a]chrysen-9-yl] (Z)-3-(4-hydroxyphenyl)prop-2-enoate 162917815 Click to see 572.90 unknown https://doi.org/10.1248/CPB.53.95
[(1R,3aR,5aR,5bR,7aR,9S,11aR,11bR,13aR,13bR)-3a,5a,5b,8,8,11a-hexamethyl-1-prop-1-en-2-yl-1,2,3,4,5,6,7,7a,9,10,11,11b,12,13,13a,13b-hexadecahydrocyclopenta[a]chrysen-9-yl] (E)-3-(4-hydroxyphenyl)prop-2-enoate 21582590 Click to see 572.90 unknown https://doi.org/10.1248/CPB.53.95
[(1R,3aR,5aR,5bR,7aR,9S,11aR,11bR,13aR,13bR)-3a,5a,5b,8,8,11a-hexamethyl-1-prop-1-en-2-yl-1,2,3,4,5,6,7,7a,9,10,11,11b,12,13,13a,13b-hexadecahydrocyclopenta[a]chrysen-9-yl] (Z)-3-(4-hydroxyphenyl)prop-2-enoate 11801224 Click to see CC(=C)C1CCC2(C1C3CCC4C5(CCC(C(C5CCC4(C3(CC2)C)C)(C)C)OC(=O)C=CC6=CC=C(C=C6)O)C)C 572.90 unknown https://doi.org/10.1248/CPB.53.95
[(1R,3aR,5aR,5bR,7aR,9S,11aS,11bR,13aR,13bS)-3a,5a,5b,8,8,11a-hexamethyl-1-prop-1-en-2-yl-1,2,3,4,5,6,7,7a,9,10,11,11b,12,13,13a,13b-hexadecahydrocyclopenta[a]chrysen-9-yl] (E)-3-(3,4-dihydroxyphenyl)prop-2-enoate 162990113 Click to see 588.90 unknown https://doi.org/10.1248/CPB.53.95
[(1R,3aR,5aR,5bR,7aR,9S,11aS,11bR,13aR,13bS)-3a,5a,5b,8,8,11a-hexamethyl-1-prop-1-en-2-yl-1,2,3,4,5,6,7,7a,9,10,11,11b,12,13,13a,13b-hexadecahydrocyclopenta[a]chrysen-9-yl] (Z)-3-(3,4-dihydroxyphenyl)prop-2-enoate 162990116 Click to see CC(=C)C1CCC2(C1C3CCC4C5(CCC(C(C5CCC4(C3(CC2)C)C)(C)C)OC(=O)C=CC6=CC(=C(C=C6)O)O)C)C 588.90 unknown https://doi.org/10.1248/CPB.53.95
[(3aR,5aR,5bR,7aR,11aR,11bR,13aR,13bR)-3a,5a,5b,8,8,11a-hexamethyl-1-prop-1-en-2-yl-1,2,3,4,5,6,7,7a,9,10,11,11b,12,13,13a,13b-hexadecahydrocyclopenta[a]chrysen-9-yl] 3-(3,4-dihydroxyphenyl)prop-2-enoate 138113695 Click to see 588.90 unknown https://doi.org/10.1002/CHIN.200533207
3-(Z)-Caffeoyllupeol 11786639 Click to see 588.90 unknown https://doi.org/10.1248/CPB.53.95
Lup-20(29)-en-3-ol, (3beta)- 521518 Click to see CC(=C)C1CCC2(C1C3CCC4C5(CCC(C(C5CCC4(C3(CC2)C)C)(C)C)O)C)C 426.70 unknown https://doi.org/10.1248/CPB.53.95
Lup-20(29)-en-3-one 323075 Click to see CC(=C)C1CCC2(C1C3CCC4C5(CCC(=O)C(C5CCC4(C3(CC2)C)C)(C)C)C)C 424.70 unknown https://doi.org/10.1248/CPB.53.95
Lupenone 92158 Click to see CC(=C)C1CCC2(C1C3CCC4C5(CCC(=O)C(C5CCC4(C3(CC2)C)C)(C)C)C)C 424.70 unknown https://doi.org/10.1002/CHIN.200533207
https://doi.org/10.1248/CPB.53.95
Lupeol 259846 Click to see 426.70 unknown https://doi.org/10.1002/CHIN.200533207
https://doi.org/10.1248/CPB.53.95

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