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Internal ID UUID643ffce7aa58f235367249
Scientific name Suaeda aegyptiaca
Authority (Hasselq.) Zohary
First published in J. Linn. Soc., Bot. 55: 635 (1957)

Ethnobotanical Use Top

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General Uses Top

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Common products:
- Seed oil: extracted from the seeds (≈8–12 % of dry seed weight); fatty‑acid profile dominated by linoleic acid (≈50–60 % of total fatty acids), with oleic (≈15–20 %) and palmitic (≈10–12 %) acids. The oil is suitable for biodiesel production.
- Dried aerial biomass: harvested shoots contain ~15–20 % crude protein on a dry‑matter basis; used as a high‑protein forage for livestock in arid, saline regions.

Industrial and craft applications:
- Biodiesel: the seed oil can be transesterified to fatty‑acid methyl esters that satisfy the key fuel‑quality specifications of ASTM D6751 and EN 14214 (including cetane number, flash point, acid value, and cold‑flow properties).

Properties relevant to use:
- Fatty‑acid composition (high linoleic acid) provides good oxidative stability and a cetane number suitable for diesel engines.
- Protein‑rich biomass (≈15–20 % CP) offers a digestible nitrogen source for ruminants.
- Halophytic physiology allows growth on soils with salinity up to ~300 mM NaCl, enabling cultivation on marginal lands without freshwater irrigation.
- The genome of S. aegyptiaca has been sequenced (publicly available in NCBI/Phytozome) and serves as a reference for functional‑genomics studies of salt tolerance.

Standards and regulation:
- Biodiesel derived from S. aegyptiaca seed oil must meet ASTM D6751 (U.S.) and EN 14214 (EU) standards for fuel quality, covering parameters such as sulfur content, flash point, and cold‑flow performance.
- Forage use is governed by national feed‑safety regulations (e.g., Codex Alimentarius guidelines for animal feed) and must comply with limits on contaminants and nutrient composition.

Sustainability and sourcing:
- As a facultative halophyte, S. aegyptiaca can be cultivated on saline or alkaline soils that are unsuitable for conventional crops, reducing competition for arable land and freshwater resources.
- Low‑input cultivation (minimal fertilizer and irrigation) yields both oil and biomass, supporting land‑reclamation projects and providing diversified income for farmers in marginal environments.

Synonyms Top

Scientific name Authority First published in
Lerchia hortensis (Forssk. ex J.F.Gmel.) Kuntze Revis. Gen. Pl. 2: 549 (1891)
Lerchia baccata (Forssk. ex J.F.Gmel.) Kuntze Revis. Gen. Pl. 2: 549 (1891)
Salsola baccata (Forssk. ex J.F.Gmel.) Poir. Encycl. 7: 298 (1806)
Suaeda hortensis Forssk. ex J.F.Gmel. in Onomat. Bot. Compl. 8: 798 (1776).
Suaeda baccata Forssk. ex J.F.Gmel. in Onomat. Bot. Compl. 8: 797 (1776).
Schanginia baccata (Forssk. ex J.F.Gmel.) Moq. Chenop. Monogr. Enum. : 119 (1840)
Schanginia hortensis (Forssk. ex J.F.Gmel.) Moq. Chenop. Monogr. Enum. : 119 (1840)
Schanginia aegyptiaca (Hasselq.) Aellen Fl. Lowland Iraq : 195 (1964)
Schoberia hortensis (Forssk. ex J.F.Gmel.) Steud. Nomencl. Bot. , ed. 2, 2: 532 (1841)
Chenopodium aegyptiacum Hasselq. Iter Palaest. : 460 (1757)
Chenopodium hortense (Forssk. ex J.F.Gmel.) Schult. Syst. Veg., ed. 15 bis 6: 268 (1820)
Enchylaena aegyptiaca (Hasselq.) Spreng. Syst. Veg. 1: 923 (1824)

Common names Top

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Language Common/alternative name
English seablite
Arabic كاكول
Arabic سويداء مصرية
German schanginia aegyptiaca
German schanginia hortensis
German suaeda hortensis
German suaeda baccata
German schanginia baccata
German chenopodium aegyptiacum
Persian سیاه شور مصری
Persian کاکل
Persian سیاهشور مصری

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

Legend for the distribution data:
- Doubtful data
- Extinct
- Introduced
- Native
  • Africa
    • Northeast Tropical Africa
      • Djibouti
      • Eritrea
      • Somalia
      • Sudan
    • Northern Africa
      • Egypt
      • Libya
  • Asia-temperate
    • Arabian Peninsula
      • Gulf States
      • Kuwait
      • Oman
      • Saudi Arabia
      • Yemen
    • Western Asia
      • Afghanistan
      • Cyprus
      • Iran
      • Iraq
      • Lebanon-Syria
      • Palestine
      • Sinai

Links to other databases Top

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Database ID/link to page
World Flora Online wfo-0000437555
Tropicos 7201441
KEW urn:lsid:ipni.org:names:167397-1
The Plant List kew-2483924
Open Tree Of Life 737778
NCBI Taxonomy 224153
IPNI 167397-1
iNaturalist 489397
GBIF 3757104
Freebase /m/0rfg_fm
Wikipedia Suaeda_aegyptiaca

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
Nanotechnology in the Diagnosis and Treatment of Antibiotic-Resistant Infections Ioannou P, Baliou S, Samonis G Antibiotics (Basel) 25-Jan-2024
PMCID:PMC10886108
doi:10.3390/antibiotics13020121
PMID:38391507
Facile biosynthesis of Ag–ZnO nanocomposites using Launaea cornuta leaf extract and their antimicrobial activity Makauki E, Mtavangu SG, Basu OD, Rwiza M, Machunda R Discov Nano 17-Nov-2023
PMCID:PMC10656379
doi:10.1186/s11671-023-03925-2
PMID:37975945
Exploring the potential of halotolerant bacteria from coastal regions to mitigate salinity stress in wheat: physiological, molecular, and biochemical insights Aizaz M, Lubna, Ahmad W, Khan I, Asaf S, Bilal S, Jan R, Asif S, Waqas M, Khan AL, Kim KM, AL-Harrasi A Front Plant Sci 22-Sep-2023
PMCID:PMC10556533
doi:10.3389/fpls.2023.1224731
PMID:37810397
Salinity-induced changes in plastoquinone pool redox state in halophytic Mesembryanthemum crystallinum L. Pilarska M, Niewiadomska E, Kruk J Sci Rep 10-Jul-2023
PMCID:PMC10333315
doi:10.1038/s41598-023-38194-7
PMID:37430104
Physicochemical properties of Kakol (Suaeda aegyptiaca) essential oil nanoemulsion and its effect on the storage quality of rainbow trout (Oncorhynchus mykiss) during cold storage Zibaee P, Shamekhi M Food Sci Nutr 15-Jun-2023
PMCID:PMC10494664
doi:10.1002/fsn3.3480
PMID:37701194
Halophytes as new model plant species for salt tolerance strategies Mann A, Lata C, Kumar N, Kumar A, Kumar A, Sheoran P Front Plant Sci 11-May-2023
PMCID:PMC10211249
doi:10.3389/fpls.2023.1137211
PMID:37251767
Edible Halophytes with Functional Properties: In Vitro Protein Digestibility and Bioaccessibility and Intestinal Absorption of Minerals and Trace Elements from Australian Indigenous Halophytes Srivarathan S, Addepalli R, Adiamo OQ, Kodagoda GK, Phan AD, Wright OR, Sultanbawa Y, Osborne S, Netzel ME Molecules 10-May-2023
PMCID:PMC10222652
doi:10.3390/molecules28104004
PMID:37241743
Cytotoxic, Antidiabetic, and Antioxidant Study of Biogenically Improvised Elsholtzia blanda and Chitosan-Assisted Zinc Oxide Nanoparticles Maheo AR, Vithiya B SM, Arul Prasad T A, Mangesh VL, Perumal T, Al-Qahtani WH, Govindasamy M ACS Omega 15-Mar-2023
PMCID:PMC10061636
doi:10.1021/acsomega.2c07530
PMID:37008090
In situ facile green synthesis of Ag–ZnO nanocomposites using Tetradenia riperia leaf extract and its antimicrobial efficacy on water disinfection Mtavangu SG, Machunda RL, van der Bruggen B, Njau KN Sci Rep 13-Sep-2022
PMCID:PMC9470730
doi:10.1038/s41598-022-19403-1
PMID:36100625
Research Advances on Molecular Mechanism of Salt Tolerance in Suaeda Yu W, Wu W, Zhang N, Wang L, Wang Y, Wang B, Lan Q, Wang Y Biology (Basel) 26-Aug-2022
PMCID:PMC9495733
doi:10.3390/biology11091273
PMID:36138752
Floristic diversity and vegetation of the az Zakhnuniyah Island, Arabian Gulf, Saudi Arabia Al-Taisan WA Heliyon 19-Jul-2022
PMCID:PMC9307451
doi:10.1016/j.heliyon.2022.e09996
PMID:35879996
Aerobiological monitoring in a desert type ecosystem: Two sampling stations of two cities (2017–2020) in Qatar Al-Nesf MA, Gharbi D, Mobayed HM, Mohammed Ali R, Tuffaha A, Dason BR, Adeli M, Sattar HA, Trigo MD PLoS One 13-Jul-2022
PMCID:PMC9278729
doi:10.1371/journal.pone.0270975
PMID:35830387
Phytochemical Compositions of Some Red Sea Halophyte Plants with Antioxidant and Anticancer Potentials Hawas UW, El-Kassem LT, Shaher FM, Al-Farawati R, Ghandourah M Molecules 25-May-2022
PMCID:PMC9182077
doi:10.3390/molecules27113415
PMID:35684352
Green Metallic Nanoparticles: Biosynthesis to Applications Chopra H, Bibi S, Singh I, Hasan MM, Khan MS, Yousafi Q, Baig AA, Rahman MM, Islam F, Emran TB, Cavalu S Front Bioeng Biotechnol 06-Apr-2022
PMCID:PMC9019488
doi:10.3389/fbioe.2022.874742
PMID:35464722
Vegetation Composition of the Halophytic Grass Aeluropus lagopoides Communities within Coastal and Inland Sabkhas of Saudi Arabia Dar BA, Assaeed AM, Al-Rowaily SL, Al-Doss AA, Abd-ElGawad AM Plants (Basel) 28-Feb-2022
PMCID:PMC8912373
doi:10.3390/plants11050666
PMID:35270136

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 / Fatty Acyls / Fatty acids and conjugates / Long-chain fatty acids
Myristic Acid 11005 Click to see 228.37 unknown https://doi.org/10.4197/SCI.16-1.4
Oleic Acid 445639 Click to see 282.50 unknown https://doi.org/10.4197/SCI.16-1.4
Palmitic Acid 985 Click to see 256.42 unknown https://doi.org/10.4197/SCI.16-1.4
Palmitoleic Acid 445638 Click to see CCCCCCC=CCCCCCCCC(=O)O 254.41 unknown https://doi.org/10.4197/SCI.16-1.4
Stearic Acid 5281 Click to see 284.50 unknown https://doi.org/10.4197/SCI.16-1.4
> Lipids and lipid-like molecules / Fatty Acyls / Lineolic acids and derivatives
Linoleic Acid 5280450 Click to see CCCCCC=CCC=CCCCCCCCC(=O)O 280.40 unknown https://doi.org/10.4197/SCI.16-1.4
Linolenic Acid 5280934 Click to see 278.40 unknown https://doi.org/10.4197/SCI.16-1.4
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Cholestane steroids / Cholesterols and derivatives
Cholesterol 5997 Click to see 386.70 unknown https://doi.org/10.4197/SCI.16-1.4
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Ergostane steroids / Ergosterols and derivatives
(3S,8S,9S,14S,17R)-17-[(2R,5R)-5,6-dimethylheptan-2-yl]-10,13-dimethyl-2,3,4,7,8,9,11,12,14,15,16,17-dodecahydro-1H-cyclopenta[a]phenanthren-3-ol 134766514 Click to see 400.70 unknown https://doi.org/10.4197/SCI.16-1.4
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Stigmastanes and derivatives
17-(5-ethyl-6-methylheptan-2-yl)-10,13-dimethyl-2,3,4,7,8,9,11,12,14,15,16,17-dodecahydro-1H-cyclopenta[a]phenanthren-3-ol 86821 Click to see CCC(CCC(C)C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)O)C)C)C(C)C 414.70 unknown https://doi.org/10.4197/SCI.16-1.4
Stigmasterol 5280794 Click to see 412.70 unknown https://doi.org/10.4197/SCI.16-1.4
> Organic acids and derivatives / Carboxylic acids and derivatives / Amino acids, peptides, and analogues / Alpha amino acids and derivatives / Alanine and derivatives
D-Alanine 71080 Click to see 89.09 unknown https://doi.org/10.4197/SCI.16-1.4
> Organic acids and derivatives / Carboxylic acids and derivatives / Amino acids, peptides, and analogues / Alpha amino acids and derivatives / Alpha amino acids / L-alpha-amino acids
L-Arginine 6322 Click to see 174.20 unknown https://doi.org/10.4197/SCI.16-1.4
Lysine 5962 Click to see C(CCN)CC(C(=O)O)N 146.19 unknown https://doi.org/10.4197/SCI.16-1.4
Threonine 6288 Click to see CC(C(C(=O)O)N)O 119.12 unknown https://doi.org/10.4197/SCI.16-1.4
> Organic acids and derivatives / Carboxylic acids and derivatives / Amino acids, peptides, and analogues / Alpha amino acids and derivatives / Aspartic acid and derivatives
D-Aspartic Acid 83887 Click to see 133.10 unknown https://doi.org/10.4197/SCI.16-1.4
> Organic acids and derivatives / Carboxylic acids and derivatives / Amino acids, peptides, and analogues / Alpha amino acids and derivatives / Glutamic acid and derivatives
L-Glutamic Acid 33032 Click to see 147.13 unknown https://doi.org/10.4197/SCI.16-1.4
> Organic acids and derivatives / Carboxylic acids and derivatives / Amino acids, peptides, and analogues / Alpha amino acids and derivatives / Histidine and derivatives
Histidine 6274 Click to see C1=C(NC=N1)CC(C(=O)O)N 155.15 unknown https://doi.org/10.4197/SCI.16-1.4
> Organic acids and derivatives / Carboxylic acids and derivatives / Amino acids, peptides, and analogues / Alpha amino acids and derivatives / Isoleucine and derivatives
l-Isoleucine 6306 Click to see CCC(C)C(C(=O)O)N 131.17 unknown https://doi.org/10.4197/SCI.16-1.4
> Organic acids and derivatives / Carboxylic acids and derivatives / Amino acids, peptides, and analogues / Alpha amino acids and derivatives / Leucine and derivatives
Leucine 6106 Click to see CC(C)CC(C(=O)O)N 131.17 unknown https://doi.org/10.4197/SCI.16-1.4
> Organic acids and derivatives / Carboxylic acids and derivatives / Amino acids, peptides, and analogues / Alpha amino acids and derivatives / Methionine and derivatives
D-Methionine 84815 Click to see CSCCC(C(=O)O)N 149.21 unknown https://doi.org/10.4197/SCI.16-1.4
> Organic acids and derivatives / Carboxylic acids and derivatives / Amino acids, peptides, and analogues / Alpha amino acids and derivatives / Phenylalanine and derivatives
D-Phenylalanine 71567 Click to see 165.19 unknown https://doi.org/10.4197/SCI.16-1.4
> Organic acids and derivatives / Carboxylic acids and derivatives / Amino acids, peptides, and analogues / Alpha amino acids and derivatives / Proline and derivatives
Proline 145742 Click to see C1CC(NC1)C(=O)O 115.13 unknown https://doi.org/10.4197/SCI.16-1.4
> Organic acids and derivatives / Carboxylic acids and derivatives / Amino acids, peptides, and analogues / Alpha amino acids and derivatives / Serine and derivatives
L-Serine 5951 Click to see 105.09 unknown https://doi.org/10.4197/SCI.16-1.4
> Organic acids and derivatives / Carboxylic acids and derivatives / Amino acids, peptides, and analogues / Alpha amino acids and derivatives / Tyrosine and derivatives
L-Tyrosine 6057 Click to see 181.19 unknown https://doi.org/10.4197/SCI.16-1.4
> Organic acids and derivatives / Carboxylic acids and derivatives / Amino acids, peptides, and analogues / Alpha amino acids and derivatives / Valine and derivatives
Valine 6287 Click to see CC(C)C(C(=O)O)N 117.15 unknown https://doi.org/10.4197/SCI.16-1.4
> Organic oxygen compounds / Organooxygen compounds / Carbohydrates and carbohydrate conjugates / Glycosyl compounds / O-glycosyl compounds
Sucrose 5988 Click to see 342.30 unknown https://doi.org/10.4197/SCI.16-1.4
> Organic oxygen compounds / Organooxygen compounds / Carbohydrates and carbohydrate conjugates / Monosaccharides / Hexoses
D-Galactose 6036 Click to see 180.16 unknown https://doi.org/10.4197/SCI.16-1.4
D-Glucose 5793 Click to see C(C1C(C(C(C(O1)O)O)O)O)O 180.16 unknown https://doi.org/10.4197/SCI.16-1.4
L-Rhamnose 25310 Click to see CC1C(C(C(C(O1)O)O)O)O 164.16 unknown https://doi.org/10.4197/SCI.16-1.4
> Organic oxygen compounds / Organooxygen compounds / Carbohydrates and carbohydrate conjugates / Monosaccharides / Pentoses
L-Arabinose 439195 Click to see 150.13 unknown https://doi.org/10.4197/SCI.16-1.4
> Organic oxygen compounds / Organooxygen compounds / Carbohydrates and carbohydrate conjugates / Sugar acids and derivatives / Glucuronic acid derivatives
D-Galacturonic Acid 439215 Click to see 194.14 unknown https://doi.org/10.4197/SCI.16-1.4
D-Glucuronic Acid 94715 Click to see C1(C(C(OC(C1O)O)C(=O)O)O)O 194.14 unknown https://doi.org/10.4197/SCI.16-1.4

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