Details Top

Internal ID UUID643fdcbdf3f9f691593326
Scientific name Acacia cambagei
Authority R.T.Baker
First published in Proc. Linn. Soc. New South Wales25: 661 (1901)

Ethnobotanical Use Top

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General Uses Top

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Common products:
Timber and utility wood products (roundwood and sawn) are the principal documented use of Acacia cambagei. The species yields very hard, dense, and durable heartwood suitable for heavy-duty applications.

Industrial and craft applications:
Occasional use as heavy construction timbers, fence posts, railway sleepers, and other outdoor structural uses where resistance to weathering and insect damage is needed. In some regions the wood is employed for mine timbers and posts in agricultural and pastoral settings.

Food and beverages (non-medicinal):
No documented non-medicinal food or beverage uses have been identified in accessible, verifiable references for this taxon.

Colorants and tanning:
No documented use as a dye, ink, or tannin source in reliable, citable sources for this species.

Wood and fiber:
Wood density is high (commonly >1,000 kg/m³ air-dry), with hard, dark, oily heartwood and notable natural durability. The high density, lignification, and extractives contribute to dimensional stability and resistance to decay in ground-contact and exposed conditions. The species is noted for splitting readily, which is advantageous in fencing and post applications.

Fragrance and cosmetics:
No verified fragrance or cosmetic uses are documented for this species.

Properties relevant to use:
High basic density, hard and heavy heartwood, and natural decay resistance contribute to performance in outdoor structural uses. The wood’s splitting tendency can reduce processing requirements for posts and rails.

Standards and regulation:
No species-specific standards or regulatory frameworks have been identified in verifiable references. As with general timber trade in Australia, normal building codes and durability classifications would govern end use, but these are not specific to A. cambagei in available sources.

Sustainability and sourcing:
Acacia cambagei occurs across arid to semi-arid regions of eastern Australia and is relatively common in parts of its range. Local availability and access are conditioned by land tenure and conservation considerations in relevant jurisdictions.

Synonyms Top

Scientific name Authority First published in
Racosperma cambagei (R.T.Baker) Pedley Austrobaileya2: 346 (1987)

Common names Top

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Language Common/alternative name
English gidgee
Estonian haisev akaatsia

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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No germination or propagation data was added yet.

Distribution (via POWO/KEW) Top

Legend for the distribution data:
- Doubtful data
- Extinct
- Introduced
- Native
  • Australasia
    • Australia
      • New South Wales
      • Northern Territory
      • Queensland
      • South Australia

Links to other databases Top

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Database ID/link to page
World Flora Online wfo-0000202385
USDA Plants ACCA25
Tropicos 13037254
KEW urn:lsid:ipni.org:names:469924-1
The Plant List ild-48740
Open Tree Of Life 628362
NCBI Taxonomy 1173637
IUCN Red List 146625333
IPNI 469924-1
iNaturalist 334763
GBIF 2980690
Freebase /m/02qfmbs
EPPO ACACB
EOL 660888
USDA GRIN 799
Wikipedia Acacia_cambagei
CMAUP NPO22812

Genomes (via NCBI) Top

No reference genome is available on NCBI yet. We are constantly monitoring for new data.

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
Terrestrial mesopredators did not increase after top-predator removal in a large-scale experimental test of mesopredator release theory Castle G, Smith D, Allen LR, Allen BL Sci Rep 14-Sep-2021
PMCID:PMC8440509
doi:10.1038/s41598-021-97634-4
PMID:34521924
Climate trends in the wood anatomy of Acacia sensu stricto (Leguminosae: Mimosoideae) Warwick NW, Hailey L, Clarke KL, Gasson PE Ann Bot 09-Mar-2017
PMCID:PMC5604571
doi:10.1093/aob/mcx019
PMID:28334287
Comparative study of antioxidant activity and validated RP-HPTLC analysis of rutin in the leaves of different Acacia species grown in Saudi Arabia Alam P, Alajmi MF, Arbab AH, Parvez MK, Siddiqui NA, Alqasoumi SI, Al-Rehaily AJ, Al-Dosari MS, Basudan OA Saudi Pharm J 05-Nov-2016
PMCID:PMC5506739
doi:10.1016/j.jsps.2016.10.010
PMID:28725144
How to keep cool in a hot desert: Torpor in two species of free-ranging bats in summer Bondarenco A, Körtner G, Geiser F Temperature (Austin) 20-Jul-2016
PMCID:PMC5079220
doi:10.1080/23328940.2016.1214334
PMID:28349087

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
> Benzenoids / Benzene and substituted derivatives / Benzoic acids and derivatives / Hydroxybenzoic acid derivatives
Protocatechuic Acid 72 Click to see 154.12 unknown via CMAUP database
> Lipids and lipid-like molecules / Fatty Acyls / Lineolic acids and derivatives
Catalpic acid 5385589 Click to see CCCCC=CC=CC=CCCCCCCCC(=O)O 278.40 unknown via CMAUP database
> Lipids and lipid-like molecules / Glycerolipids / Glycosylglycerols / Glycosyldiacylglycerols / 1,2-diacyl-3-O-beta-D-galactosyl-sn-glycerols
[(2S)-2-[(9Z,12Z)-octadeca-9,12-dienoyl]oxy-3-[(2R,3R,4S,5R,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxypropyl] (Z)-octadec-9-enoate 10509461 Click to see CCCCCCCCC=CCCCCCCCC(=O)OCC(COC1C(C(C(C(O1)CO)O)O)O)OC(=O)CCCCCCCC=CCC=CCCCCC 781.10 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Diterpenoids
(1R,2R,4bR,6R,7R,8aS)-2-ethenyl-1,6,7-trihydroxy-2,4b,8,8-tetramethyl-1,5,6,7,8a,9-hexahydrophenanthren-3-one 56954823 Click to see CC1(C2CC=C3C(C(C(=O)C=C3C2(CC(C1O)O)C)(C)C=C)O)C 332.40 unknown via CMAUP database
(1R,4S,6S,9S,10S,13S)-6-hydroxy-5,5,9,13-tetramethyltetracyclo[11.2.1.01,10.04,9]hexadec-14-ene-7,12-dione 5352023 Click to see CC1(C2CCC34CC(C=C3)(C(=O)CC4C2(CC(=O)C1O)C)C)C 316.40 unknown via CMAUP database
(2R,4aS,4bS,7R,8aS)-2-ethenyl-7-hydroxy-2,4b,8,8-tetramethyl-4,4a,5,6,7,8a,9,10-octahydrophenanthren-3-one 101448906 Click to see 302.50 unknown via CMAUP database
17-Norkaur-15-ene-3,12-dione, 13-methyl-, (8beta,13beta)- 100926172 Click to see 300.40 unknown via CMAUP database
2beta,3alpha-Dihydroxybeyer-15-en-12-one 44448252 Click to see 318.40 unknown via CMAUP database
Beyerene 107412 Click to see 272.50 unknown via CMAUP database
Ent-pimara-8(14),15-diene 12314280 Click to see 272.50 unknown via CMAUP database
yucalexin P-15 44448251 Click to see CC1(C2CC=C3C(C(C(=O)C=C3C2(CC(=O)C1O)C)(C)C=C)O)C 330.40 unknown via CMAUP database
yucalexin P-17 44448241 Click to see 318.40 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Diterpenoids / Kaurane diterpenoids
Ent-Kaurene 11966109 Click to see 272.50 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Diterpenoids / Villanovane, atisane, trachylobane or helvifulvane diterpenoids / Atisane diterpenoids
Atis-13-en-3-one, 16-hydroxy-, (5beta,8alpha,9beta,10alpha,12alpha)- 100926173 Click to see 302.50 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Sesterterpenoids / Scalarane sesterterpenoids
(2R,4aR,6aR,6bR,8aR,12aR,14aS,14bR)-2,4a,6b,9,9,12a,14a-heptamethyl-10-oxo-3,4,5,6a,7,8,8a,11,12,13,14,14b-dodecahydro-1H-picene-2-carboxylic acid 102134163 Click to see CC1(C2CCC3(C(C2(CCC1=O)C)CCC4(C3=CCC5(C4CC(CC5)(C)C(=O)O)C)C)C)C 454.70 unknown via CMAUP database
Isotaraxerol 12443227 Click to see CC1(CCC2(CC=C3C4(CCC5C(C(CCC5(C4CCC3(C2C1)C)C)O)(C)C)C)C)C 426.70 unknown via CMAUP database
Taraxerol 92097 Click to see 426.70 unknown via CMAUP database
Taraxerone 92785 Click to see 424.70 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Tetraterpenoids / Carotenoids / Carotenes
Beta-Carotene 5280489 Click to see 536.90 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Triterpenoids
(4aS,6aR,6bS,8aR,12aR,14aS,14bR)-4,4,6a,6b,8a,11,11,14b-octamethyl-2,4a,5,6,7,8,9,10,12,12a,14,14a-dodecahydro-1H-picen-3-one 38359273 Click to see 424.70 unknown via CMAUP database
Beta-Amyrin 73145 Click to see CC1(CCC2(CCC3(C(=CCC4C3(CCC5C4(CCC(C5(C)C)O)C)C)C2C1)C)C)C 426.70 unknown via CMAUP database
beta-Amyrone 12306160 Click to see CC1(CCC2(CCC3(C(=CCC4C3(CCC5C4(CCC(=O)C5(C)C)C)C)C2C1)C)C)C 424.70 unknown via CMAUP database
Lupenone 92158 Click to see CC(=C)C1CCC2(C1C3CCC4C5(CCC(=O)C(C5CCC4(C3(CC2)C)C)(C)C)C)C 424.70 unknown via CMAUP database
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Stigmastanes and derivatives
(3S,8S,9S,10R,13R,14R,17R)-17-[(E,1R,4S)-4-ethyl-1,5-dimethyl-hex-2-enyl]-8,10,13-trimethyl-1,2,3,4,7,9,11,12,14,15,16,17-dodecahydrocyclopenta[a]phenanthren-3-ol 23246947 Click to see 426.70 unknown via CMAUP database
(8S,9S,10R,13R,14S,17R)-17-[(2R,5R)-5-ethyl-6-methylheptan-2-yl]-10,13-dimethyl-1,2,8,9,11,12,14,15,16,17-decahydrocyclopenta[a]phenanthren-3-one 12943207 Click to see 410.70 unknown via CMAUP database
Sitogluside 5742590 Click to see CCC(CCC(C)C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)OC5C(C(C(C(O5)CO)O)O)O)C)C)C(C)C 576.80 unknown via CMAUP database
> Organic oxygen compounds / Organooxygen compounds / Carbohydrates and carbohydrate conjugates / Glycosyl compounds / Cyanogenic glycosides
Epilotaustralin 185818 Click to see CCC(C)(C#N)OC1C(C(C(C(O1)CO)O)O)O 261.27 unknown via CMAUP database
Linamarin 11128 Click to see 247.24 unknown via CMAUP database
> Organic oxygen compounds / Organooxygen compounds / Carbohydrates and carbohydrate conjugates / Glycosyl compounds / O-glycosyl compounds
2-((6-O-(beta-D-apiofuranosyl)beta-D-glucopyranosyl)oxy)propane 10316099 Click to see 354.35 unknown via CMAUP database
ethyl beta-D-glucopyranoside 121667 Click to see CCOC1C(C(C(C(O1)CO)O)O)O 208.21 unknown via CMAUP database
> Phenylpropanoids and polyketides / Coumarins and derivatives / Coumarin glycosides
Esculin 5281417 Click to see C1=CC(=O)OC2=CC(=C(C=C21)OC3C(C(C(C(O3)CO)O)O)O)O 340.28 unknown via CMAUP database
Scopolin 439514 Click to see COC1=C(C=C2C(=C1)C=CC(=O)O2)OC3C(C(C(C(O3)CO)O)O)O 354.31 unknown via CMAUP database
> Phenylpropanoids and polyketides / Coumarins and derivatives / Hydroxycoumarins / 6,7-dihydroxycoumarins
Esculetin 5281416 Click to see 178.14 unknown via CMAUP database
> Phenylpropanoids and polyketides / Coumarins and derivatives / Hydroxycoumarins / 7-hydroxycoumarins
Scopoletin 5280460 Click to see 192.17 unknown via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavans / Catechins
Catechin 9064 Click to see 290.27 unknown via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid O-glycosides / Flavonoid-3-O-glycosides
Kaempferol-3-O-Rutinoside 5318767 Click to see 594.50 unknown via CMAUP database
Rutin 5280805 Click to see 610.50 unknown via CMAUP database

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