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Details Top

Internal ID UUID64400ed25403b475451439
Scientific name Calligonum leucocladum
Authority Bunge
First published in Beitr. Fl. Russl. : 309 (1852)

Description Top

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Synonyms Top

Scientific name Authority First published in
Pterococcus aphyllus Kar. & Kir. Bull. Soc. Imp. Naturalistes Moscou 15(2): 443. 1842
Pterococcus leucocladus Schrenk Bull. Cl. Phys.-Math. Acad. Imp. Sci. Saint-Pétersbourg 3: 211 (1845)
Calligonum anfractuosum Bunge Beitr. Fl. Russl. : 311 (1852)
Calligonum leucocladum var. flexuoasus Ledeb.
Calligonum leucocladum var. strictum Bodenb.
Calligonum alatiforme subsp. roseum Soskov
Calligonum lanciculatum Pavlov Repert. Spec. Nov. Regni Veg. 33: 148. 1933
Calligonum quadripterum Korov. ex Pavl.
Calligonum uzunachmatense Tkatsch.

Common names Top

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Language Common/alternative name
Persian اسکنبیل خراسانی
Kazakh Ақжүзгін
Chinese 红紫珠
Chinese 淡枝沙拐枣

Subspecies (abbr. subsp./ssp.) Top

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Name Authority First published in
Calligonum leucocladum subsp. elegans (Drob.) Soskov Spisok Rast. Gerb. Fl. S.S.S.R. 103-106: 30 (1972)

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
  • Asia-temperate
    • China
      • Xinjiang
    • Middle Asia
      • Kazakhstan
      • Kirgizstan
      • Tadzhikistan
      • Turkmenistan
      • Uzbekistan
    • Western Asia
      • Iran

Links to other databases Top

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Database ID/link to page
World Flora Online wfo-0000580446
USDA Plants CALE47
Tropicos 26000024
KEW urn:lsid:ipni.org:names:693354-1
The Plant List kew-2692565
Open Tree Of Life 756948
Observations.org 131894
NCBI Taxonomy 1202986
IPNI 693354-1
iNaturalist 820881
GBIF 6391706
Freebase /m/0gh7kp5
EOL 2905869
Elurikkus 3300
USDA GRIN 404428
Wikipedia Calligonum_leucocladum

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
Capturing the microbial dark matter in desert soils using culturomics-based metagenomics and high-resolution analysis Li S, Lian WH, Han JR, Ali M, Lin ZL, Liu YH, Li L, Zhang DY, Jiang XZ, Li WJ, Dong L NPJ Biofilms Microbiomes 22-Sep-2023
PMCID:PMC10516943
doi:10.1038/s41522-023-00439-8
PMID:37736746
Syntrichia caninervis adapt to mercury stress by altering submicrostructure and physiological properties in the Gurbantünggüt Desert Mao Y, Liu W, Yang X, Chang Y, Yang T, Wang X, Chen Y Sci Rep 09-Jul-2022
PMCID:PMC9271083
doi:10.1038/s41598-022-15822-2
PMID:35810254
Wing loading, not terminal velocity, is the best parameter to predict capacity of diaspores for secondary wind dispersal Liang W, Liu Z, Liu M, Qin X, Baskin CC, Baskin JM, Xin Z, Wang Z, Su Z, Zhou Q J Exp Bot 03-Apr-2020
PMCID:PMC7475251
doi:10.1093/jxb/eraa170
PMID:32242240
Crepis desertorum (Asteraceae, Cichorieae), a new species from northern Xinjiang (China) based on morphological and molecular data Qiu J, Zhang J, Gao T, Tan D Plant Divers 12-Dec-2019
PMCID:PMC7195582
doi:10.1016/j.pld.2019.11.003
PMID:32373765
Germination heterochrony in annual plants of Salsola L.: an effective survival strategy in changing environments Liu HF, Liu T, Han ZQ, Luo N, Liu ZC, Hao XR Sci Rep 26-Apr-2018
PMCID:PMC5920052
doi:10.1038/s41598-018-23319-0
PMID:29700346
Dataset of pollen morphological traits of 56 dominant species among desert vegetation in the eastern arid central Asia Lu KQ, Xie G, Li M, Li JF, Trivedi A, Ferguson DK, Yao YF, Wang YF Data Brief 31-Mar-2018
PMCID:PMC5996618
doi:10.1016/j.dib.2018.03.122
PMID:29900271
Phytochemical and biological research of Polygoneae medicinal resources Hao DC, Gu XJ, Xiao PG Medicinal Plants 03-Jul-2015
PMCID:PMC7158354
doi:10.1016/B978-0-08-100085-4.00012-8
The Relationship between Diaspore Characteristics with Phylogeny, Life History Traits, and Their Ecological Adaptation of 150 Species from the Cold Desert of Northwest China Liu HL, Zhang DY, Duan SM, Wang XY, Song MF ScientificWorldJournal 30-Jan-2014
PMCID:PMC3925582
doi:10.1155/2014/510343
PMID:24605054
Research on chemical characteristics of soil salt crusts with saline groundwater drip-irrigation in the Tarim Desert Highway Shelterbelt Zhang J, Xu X, Lei J, Li S Springerplus 11-Dec-2013
PMCID:PMC3973407
doi:10.1186/2193-1801-2-S1-S5
PMID:24701388
Similarity and difference in vegetation structure of three desert shrub communities under the same temperate climate but with different microhabitats Tao Y, Zhang YM, Downing A Bot Stud 02-Dec-2013
PMCID:PMC5432825
doi:10.1186/1999-3110-54-59
PMID:28510895
Storage/Turnover Rate of Inorganic Carbon and Its Dissolvable Part in the Profile of Saline/Alkaline Soils Wang Y, Wang Z, Li Y PLoS One 29-Nov-2013
PMCID:PMC3843718
doi:10.1371/journal.pone.0082029
PMID:24312399
Plant traits with different dimensions of shrubs represent different spatial patterns and plant-to-plant interactions in a temperate desert Tao Y, Zhang YM EXCLI J 19-Jul-2013
PMCID:PMC4653720
PMID:26600733
Detection and Extraction of Anti-Listerial Compounds from Calligonum Comosum, A Medicinal Plant from Arid Regions of Tunisia Riadh H, Imen F, Abdelmajid Z, Sinda F Afr J Tradit Complement Altern Med 02-Apr-2011
PMCID:PMC3252229
PMID:22468012
Flavonoids from the leaves of Calligonum leucocladum N. S. Dubinin, V. I. Litvinenko, V. V. Vorovskii Springer Science and Business Media LLC 20-Nov-2004
doi:10.1007/BF00571239

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
> Organic oxygen compounds / Organooxygen compounds / Alcohols and polyols / Cyclitols and derivatives / Quinic acids and derivatives
Chlorogenic Acid 1794427 Click to see C1C(C(C(CC1(C(=O)O)O)OC(=O)C=CC2=CC(=C(C=C2)O)O)O)O 354.31 unknown https://doi.org/10.1007/BF00571239
Neochlorogenic acid 5280633 Click to see C1C(C(C(CC1(C(=O)O)O)OC(=O)C=CC2=CC(=C(C=C2)O)O)O)O 354.31 unknown https://doi.org/10.1007/BF00571239
> Phenylpropanoids and polyketides / Cinnamic acids and derivatives / Hydroxycinnamic acids and derivatives / Hydroxycinnamic acids
Caffeic Acid 689043 Click to see C1=CC(=C(C=C1C=CC(=O)O)O)O 180.16 unknown https://doi.org/10.1007/BF00571239
Ferulic acid 445858 Click to see COC1=C(C=CC(=C1)C=CC(=O)O)O 194.18 unknown https://doi.org/10.1007/BF00571239
Isoferulic acid 736186 Click to see COC1=C(C=C(C=C1)C=CC(=O)O)O 194.18 unknown https://doi.org/10.1007/BF00571239
p-Coumaric acid 637542 Click to see C1=CC(=CC=C1C=CC(=O)O)O 164.16 unknown https://doi.org/10.1007/BF00571239
Sinapinic acid 637775 Click to see COC1=CC(=CC(=C1O)OC)C=CC(=O)O 224.21 unknown https://doi.org/10.1007/BF00571239
> Phenylpropanoids and polyketides / Flavonoids / Flavans / Flavanones / Flavanonols
(+)-Epiaromadendrin 11449086 Click to see C1=CC(=CC=C1C2C(C(=O)C3=C(C=C(C=C3O2)O)O)O)O 288.25 unknown https://doi.org/10.1007/BF00571239
3,5,7-Trihydroxy-2-(4-hydroxyphenyl)-2,3-dihydrochromen-4-one 662 Click to see C1=CC(=CC=C1C2C(C(=O)C3=C(C=C(C=C3O2)O)O)O)O 288.25 unknown https://doi.org/10.1007/BF00571239
Aromadendrin 122850 Click to see C1=CC(=CC=C1C2C(C(=O)C3=C(C=C(C=C3O2)O)O)O)O 288.25 unknown https://doi.org/10.1007/BF00571239
> Phenylpropanoids and polyketides / Flavonoids / Flavones / Flavonols
Kaempferol 5280863 Click to see C1=CC(=CC=C1C2=C(C(=O)C3=C(C=C(C=C3O2)O)O)O)O 286.24 unknown https://doi.org/10.1007/BF00571239
Quercetin 5280343 Click to see C1=CC(=C(C=C1C2=C(C(=O)C3=C(C=C(C=C3O2)O)O)O)O)O 302.23 unknown https://doi.org/10.1007/BF00571239
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid O-glycosides / Flavonoid-3-O-glycosides
2-(3,4-Dihydroxy-phenyl)-5,7-dihydroxy-3-(3,4,5-trihydroxy-6-methyl-tetrahydro-pyran-2-yloxy)-chromen-4-one 5353915 Click to see CC1C(C(C(C(O1)OC2=C(OC3=CC(=CC(=C3C2=O)O)O)C4=CC(=C(C=C4)O)O)O)O)O 448.40 unknown https://doi.org/10.1007/BF00571239
2-(3,4-dihydroxyphenyl)-5,7-dihydroxy-3-[(2S,3S,4R,5R,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxychromen-4-one 51521831 Click to see C1=CC(=C(C=C1C2=C(C(=O)C3=C(C=C(C=C3O2)O)O)OC4C(C(C(C(O4)CO)O)O)O)O)O 464.40 unknown https://doi.org/10.1007/BF00571239
2-(3,4-dihydroxyphenyl)-5,7-dihydroxy-3-[(2S,3S,4R,5R,6S)-3,4,5-trihydroxy-6-methyloxan-2-yl]oxychromen-4-one 26339717 Click to see CC1C(C(C(C(O1)OC2=C(OC3=CC(=CC(=C3C2=O)O)O)C4=CC(=C(C=C4)O)O)O)O)O 448.40 unknown https://doi.org/10.1007/BF00571239
Hyperoside 5281643 Click to see C1=CC(=C(C=C1C2=C(C(=O)C3=C(C=C(C=C3O2)O)O)OC4C(C(C(C(O4)CO)O)O)O)O)O 464.40 unknown https://doi.org/10.1007/BF00571239

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