Populus euphratica - Unknown
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Internal ID UUID64403686145d4340108724
Scientific name Populus euphratica
Authority Olivier
First published in Voy. Emp. Othoman , ed. Quatra, 3: 449 (1807)

Description Top

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Populus euphratica, also known as the Euphrates poplar, is a deciduous tree in the willow family. It can grow up to 15 meters tall and has a bent and forked stem with thick, olive-green bark. The leaves are highly variable in shape and the flowers are borne as catkins. This species is found naturally in a wide range, from North Africa to western China, and can be found in dry temperate and subtropical forests. It is an important component of Tugay floodplain ecosystems and is tolerant of saline and brackish water. The Euphrates poplar is used for various purposes such as fodder for livestock, timber, and afforestation programs. Its bark also has medicinal properties. However, its forests have been greatly reduced due to human activities.

Synonyms Top

Scientific name Authority First published in
Populus bonnetiana Dode Bull. Soc. Hist. Nat. Autun 18: 175 (1905)
Populus mauritanica Dode Bull. Soc. Hist. Nat. Autun 18: 174 (1905)
Populus illicitana Dode Bull. Soc. Dendrol. France 1908: 163 (1908)
Turanga mauritanica (Dode) Kimura Sci. Rep. Tohoku Imp. Univ., Ser. 4, Biol. 13: 387 (1938)
Turanga bonnetiana (Dode) Kimura Sci. Rep. Tohoku Imp. Univ., Ser. 4, Biol. 13: 387 (1938)
Turanga illicitana (Dode) Kimura Sci. Rep. Tohoku Imp. Univ., Ser. 4, Biol. 13: 388 (1938)
Balsamiflua ariana (Dode) Kimura Sci. Rep. Tohoku Imp. Univ., Ser. 4, Biol. 14: 192 (1939)
Balsamiflua bonnetiana (Dode) Kimura Sci. Rep. Tohoku Imp. Univ., Ser. 4, Biol. 14: 192 (1939)
Balsamiflua deltoides Griff. Not. Pl. Asiat. 4: 382 (1854)
Balsamiflua diversifolia (Schrenk) Kimura Sci. Rep. Tohoku Imp. Univ., Ser. 4, Biol. 14: 192 (1939)
Balsamiflua euphratica (Oliv.) Kimura Sci. Rep. Tohoku Imp. Univ., Ser. 4, Biol. 14: 191 (1939)
Balsamiflua illicitana (Dode) Kimura Sci. Rep. Tohoku Imp. Univ., Ser. 4, Biol. 14: 193 (1939)
Balsamiflua litwinowiana (Dode) Kimura Sci. Rep. Tohoku Imp. Univ., Ser. 4, Biol. 14: 192 (1939)
Balsamiflua mauritanica (Dode) Kimura in Sc. Rep. Tohoku Imp. Univ. Ser. IV. (Biol.) xiv. 192 (1939).
Populus ariana Dode Bull. Soc. Hist. Nat. Autun 18: 174 (1905)
Populus diversifolia Schrenk Enum. Pl. Nov. 2: 15 (1842)
Turanga diversifolia (Schrenk) Kimura Sci. Rep. Tohoku Imp. Univ., Ser. 4, Biol. 13: 387 (1938)
Turanga euphratica (Olivier) Kimura Sci. Rep. Tohoku Imp. Univ., Ser. 4, Biol. 13: 386 (1938)
Populus transcaucasica Jarm. ex Grossh.
Turanga ariana (Dode) Kimura Sci. Rep. Tohoku Imp. Univ., Ser. 4, Biol. 13: 387 (1938)
Populus litwinowiana Dode Bull. Soc. Hist. Nat. Autun 18: 175 (1905)
Turanga litwinowiana (Dode) Kimura Sci. Rep. Tohoku Imp. Univ., Ser. 4, Biol. 13: 387 (1938)

Common names Top

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Language Common/alternative name
English euphrates poplar
Spanish alamo del plufrates
Spanish Álamo del plufrates
Spanish chopo de elche
Arabic صفصاف
Arabic غرب
Arabic حور الفرات
Arabic مرسيس
Arabic الحور الفراتي
Arabic حور فراتي
German euphrat-pappel
German euphratpappel
Persian پده
Finnish eufratinpoppeli
French peuplier charab
Hebrew צפצפת הפרת
Armenian եփրատի բարդի
Japanese コトカケヤナギ
Japanese コトカケヤナギ(ユーフラテスポプラ)
Kazakh Тораңғы
Latvian eifratas papele
Polish topola eufracka
Russian Туранга евфратская
Russian Тополь евфратский
Russian Туранга ефратская
Turkish fırat kavağı
udm Евфратысь тополь
Chinese 胡桐泪
Chinese 胡杨

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
  • Asia-temperate
    • Caucasus
      • Transcaucasus
    • China
      • China North-central
      • Inner Mongolia
      • Qinghai
      • Xinjiang
    • Middle Asia
      • Kazakhstan
      • Tadzhikistan
      • Turkmenistan
      • Uzbekistan
    • Mongolia
      • Mongolia
    • Western Asia
      • Afghanistan
      • Iran
      • Iraq
      • Lebanon-Syria
      • Palestine
      • Turkey

Links to other databases Top

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Database ID/link to page
World Flora Online wfo-0000928122
Tropicos 28300581
KEW urn:lsid:ipni.org:names:776672-1
The Plant List kew-5000084
Open Tree Of Life 164191
Observations.org 124686
NCBI Taxonomy 75702
IUCN Red List 19178509
IPNI 776672-1
iNaturalist 82162
GBIF 3804846
Freebase /m/0t53_dj
EPPO POPEU
EOL 2871975
USDA GRIN 29386
Wikipedia Populus_euphratica

Genomes (via NCBI) Top

Below is displayed the reference genome only!
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Accession Assembly
Name Level Submitter Released Coverage Size
GCF_000495115.2 PopEup_1.0 Scaffold Lanzhou University 2014-08-12 N/A 471.99 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
Molecular Mechanisms of CBL-CIPK Signaling Pathway in Plant Abiotic Stress Tolerance and Hormone Crosstalk Kaya C, Uğurlar F, Adamakis ID Int J Mol Sci 06-May-2024
PMCID:PMC11084290
doi:10.3390/ijms25095043
PMID:38732261
Monitoring and evaluation of vegetation restoration in the Ebinur Lake Wetland National Nature Reserve under lockdown protection Xia N, Tang Y, Tang M, Quan W, Xu Z, Zhang B, Xiao Y, Ma Y Front Plant Sci 18-Apr-2024
PMCID:PMC11063322
doi:10.3389/fpls.2024.1332788
PMID:38699539
Impact of meteorological variability on diurnal and seasonal net ecosystem productivity in a desert riparian forest ecosystem Teng D, Gong X, He X, Wang J, Lv G, Wang J, Yang X Front Plant Sci 18-Apr-2024
PMCID:PMC11063279
doi:10.3389/fpls.2024.1332192
PMID:38699537
Genome-wide identification and stress response analysis of BcaCPK gene family in amphidiploid Brassica carinata Zuo D, Lei S, Qian F, Gu L, Wang H, Du X, Zeng T, Zhu B BMC Plant Biol 17-Apr-2024
PMCID:PMC11022436
doi:10.1186/s12870-024-05004-9
Ecological risk assessment of landscape in arid area watersheds under ecological water conveyance: A case study of Taitema Lake Lv Z, Li S, Xu X, Lei J, Peng Z Heliyon 14-Apr-2024
PMCID:PMC11036042
doi:10.1016/j.heliyon.2024.e29575
PMID:38655318
Analysis of Leaf and Soil Nutrients, Microorganisms and Metabolome in the Growth Period of Idesia polycarpa Maxim Zhang T, Wang S, Rana S, Wang Y, Liu Z, Cai Q, Geng X, Yuan Q, Yang Y, Miao C, Xue X, Dai L, Li Z Microorganisms 07-Apr-2024
PMCID:PMC11051756
doi:10.3390/microorganisms12040746
PMID:38674690
Overexpression of a Fragaria vesca NAM, ATAF, and CUC (NAC) Transcription Factor Gene (FvNAC29) Increases Salt and Cold Tolerance in Arabidopsis thaliana Li W, Li H, Wei Y, Han J, Wang Y, Li X, Zhang L, Han D Int J Mol Sci 06-Apr-2024
PMCID:PMC11012600
doi:10.3390/ijms25074088
PMID:38612898
Metabolic niches in the rhizosphere microbiome: dependence on soil horizons, root traits and climate variables in forest ecosystems Maitra P, Hrynkiewicz K, Szuba A, Jagodziński AM, Al-Rashid J, Mandal D, Mucha J Front Plant Sci 05-Apr-2024
PMCID:PMC11026606
doi:10.3389/fpls.2024.1344205
PMID:38645395
Comparative genomic analysis of the Growth-Regulating Factors-Interacting Factors (GIFs) in six Salicaceae species and functional analysis of PeGIF3 reveals their regulatory role in Populus heteromorphic leaves Yang Y, Sun J, Qiu C, Jiao P, Wang H, Wu Z, Li Z BMC Genomics 28-Mar-2024
PMCID:PMC10976704
doi:10.1186/s12864-024-10221-5
PMID:38549059
Genome-Wide Analysis of the Xyloglucan Endotransglucosylase/Hydrolase (XTH) Gene Family: Expression Pattern during Magnesium Stress Treatment in the Mulberry Plant (Morus alba L.) Leaves Danso B, Ackah M, Jin X, Ayittey DM, Amoako FK, Zhao W Plants (Basel) 21-Mar-2024
PMCID:PMC10975095
doi:10.3390/plants13060902
PMID:38592929
Genome-wide identification and characterization of protein phosphatase 2C (PP2C) gene family in sunflower (Helianthus annuus L.) and their expression profiles in response to multiple abiotic stresses Akter N, Islam MS, Rahman MS, Zohra FT, Rahman SM, Manirujjaman M, Sarkar MA PLoS One 20-Mar-2024
PMCID:PMC10954154
doi:10.1371/journal.pone.0298543
PMID:38507444
Morphological, Anatomical, and Physiological Characteristics of Heteroblastic Acacia melanoxylon Grown under Weak Light Bai X, Chen Z, Chen M, Zeng B, Li X, Tu P, Hu B Plants (Basel) 18-Mar-2024
PMCID:PMC10974800
doi:10.3390/plants13060870
PMID:38592868
FvMYB108, a MYB Gene from Fragaria vesca, Positively Regulates Cold and Salt Tolerance of Arabidopsis Song P, Yang R, Jiao K, Guo B, Zhang L, Li Y, Zhang K, Zhou S, Wu X, Li X Int J Mol Sci 17-Mar-2024
PMCID:PMC10970457
doi:10.3390/ijms25063405
PMID:38542376
A GASA Protein Family Gene, CmGEG, Inhibits Petal Growth in Chrysanthemum He Z, Jiang R, Wang X, Wang Y Int J Mol Sci 16-Mar-2024
PMCID:PMC10970651
doi:10.3390/ijms25063367
PMID:38542341
Effect of hydrogen sulfide (H2S) on the growth and development of tobacco seedlings in absence of stress Dai J, Wen D, Li H, Yang J, Rao X, Yang Y, Yang J, Yang C, Yu J BMC Plant Biol 02-Mar-2024
PMCID:PMC10908218
doi:10.1186/s12870-024-04819-w
PMID:38429726

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 / Benzoic acids
Benzoic Acid 243 Click to see C1=CC=C(C=C1)C(=O)O 122.12 unknown https://doi.org/10.1016/0031-9422(91)85032-U
> Benzenoids / Benzene and substituted derivatives / Benzoic acids and derivatives / Hydroxybenzoic acid derivatives
3,4-Dihydroxybenzoic acid 72 Click to see C1=CC(=C(C=C1C(=O)O)O)O 154.12 unknown https://doi.org/10.1016/0031-9422(91)85032-U
4-Hydroxybenzoic acid 135 Click to see C1=CC(=CC=C1C(=O)O)O 138.12 unknown https://doi.org/10.1016/0031-9422(91)85032-U
https://doi.org/10.1007/S10600-008-0003-2
> Benzenoids / Benzene and substituted derivatives / Benzoic acids and derivatives / Hydroxybenzoic acid derivatives / Gallic acid and derivatives
Syringic acid 10742 Click to see COC1=CC(=CC(=C1O)OC)C(=O)O 198.17 unknown https://doi.org/10.1016/0031-9422(91)85032-U
> Benzenoids / Benzene and substituted derivatives / Benzoic acids and derivatives / Methoxybenzoic acids and derivatives / M-methoxybenzoic acids and derivatives
Vanillic Acid 8468 Click to see COC1=C(C=CC(=C1)C(=O)O)O 168.15 unknown https://doi.org/10.1016/0031-9422(91)85032-U
> Benzenoids / Benzene and substituted derivatives / Benzoic acids and derivatives / Methoxybenzoic acids and derivatives / O-methoxybenzoic acids and derivatives
3-Hydroxy-2-methoxybenzoic acid 13434501 Click to see COC1=C(C=CC=C1O)C(=O)O 168.15 unknown https://doi.org/10.1007/S10600-008-0003-2
> Benzenoids / Phenols / Methoxyphenols
2-(4'-Hydroxy-3'-methoxyphenyl)-2-oxoacetamide 129881716 Click to see COC1=C(C=CC(=C1)C(=O)C(=O)N)O 195.17 unknown https://doi.org/10.1007/S10600-008-0003-2
2-Propenal, 3-(4-hydroxy-3-methoxyphenyl)- 9984 Click to see COC1=C(C=CC(=C1)C=CC=O)O 178.18 unknown https://doi.org/10.1007/S10600-008-0003-2
2-Propenal, 3-(4-hydroxy-3,5-dimethoxyphenyl)- 119216 Click to see COC1=CC(=CC(=C1O)OC)C=CC=O 208.21 unknown https://doi.org/10.1007/S10600-008-0003-2
4-Hydroxy-3-methoxycinnamaldehyde 5280536 Click to see COC1=C(C=CC(=C1)C=CC=O)O 178.18 unknown https://doi.org/10.1007/S10600-008-0003-2
Sinapaldehyde 5280802 Click to see COC1=CC(=CC(=C1O)OC)C=CC=O 208.21 unknown https://doi.org/10.1007/S10600-008-0003-2
Syringaldehyde 8655 Click to see COC1=CC(=CC(=C1O)OC)C=O 182.17 unknown https://doi.org/10.1016/0031-9422(91)85032-U
https://doi.org/10.1007/S10600-008-0003-2
Vanillin 1183 Click to see COC1=C(C=CC(=C1)C=O)O 152.15 unknown https://doi.org/10.1007/S10600-008-0003-2
https://doi.org/10.1016/0031-9422(91)85032-U
Vanillyl alcohol 62348 Click to see COC1=C(C=CC(=C1)CO)O 154.16 unknown https://doi.org/10.1016/0031-9422(91)85032-U
> Lipids and lipid-like molecules / Fatty Acyls / Fatty acids and conjugates / Very long-chain fatty acids
Hexacosanoic acid 10469 Click to see CCCCCCCCCCCCCCCCCCCCCCCCCC(=O)O 396.70 unknown https://doi.org/10.1007/S10600-008-0003-2
> Lipids and lipid-like molecules / Fatty Acyls / Fatty alcohols
1-Hexatriacontanol 9806786 Click to see CCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCO 523.00 unknown https://doi.org/10.1007/S10600-008-0003-2
> 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/10.1007/S10600-008-0003-2
Beta-Sitosterol 222284 Click to see CCC(CCC(C)C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)O)C)C)C(C)C 414.70 unknown https://doi.org/10.1007/S10600-008-0003-2
> Organic oxygen compounds / Organooxygen compounds / Carbohydrates and carbohydrate conjugates / Glycosyl compounds / Phenolic glycosides
Salicin 439503 Click to see C1=CC=C(C(=C1)CO)OC2C(C(C(C(O2)CO)O)O)O 286.28 unknown https://doi.org/10.1016/0031-9422(91)85032-U
> Organic oxygen compounds / Organooxygen compounds / Carbonyl compounds / Benzaldehydes / Hydroxybenzaldehydes
4-Hydroxybenzaldehyde 126 Click to see C1=CC(=CC=C1C=O)O 122.12 unknown https://doi.org/10.1016/0031-9422(91)85032-U
Protocatechualdehyde 8768 Click to see C1=CC(=C(C=C1C=O)O)O 138.12 unknown https://doi.org/10.1016/0031-9422(91)85032-U
> Organic oxygen compounds / Organooxygen compounds / Carbonyl compounds / Ketones / Beta-hydroxy ketones
2,6-Dimethoxy-1-acetonylquinol 241783 Click to see CC(=O)CC1(C(=CC(=O)C=C1OC)OC)O 226.23 unknown https://doi.org/10.1007/S10600-008-0003-2
> Organic oxygen compounds / Organooxygen compounds / Carbonyl compounds / Phenylketones / Alkyl-phenylketones
3-Hydroxy-1-(4-hydroxy-3,5-dimethoxyphenyl)-1-propanone 75142 Click to see COC1=C(C=CC(=C1)C(=O)CCO)O 196.20 unknown https://doi.org/10.1007/S10600-008-0003-2
Acetovanillone 2214 Click to see CC(=O)C1=CC(=C(C=C1)O)OC 166.17 unknown https://doi.org/10.1007/S10600-008-0003-2
> Phenylpropanoids and polyketides / Cinnamic acids and derivatives / Hydroxycinnamic acids and derivatives / Coumaric acids and derivatives
1-Caffeoylglycerol 5315606 Click to see C1=CC(=C(C=C1C=CC(=O)OCC(CO)O)O)O 254.24 unknown https://doi.org/10.1016/0031-9422(91)85032-U
Benzyl ferulate 7766335 Click to see COC1=C(C=CC(=C1)C=CC(=O)OCC2=CC=CC=C2)O 284.31 unknown https://doi.org/10.1016/0031-9422(91)85032-U
Glyceryl ferulate 11311691 Click to see COC1=C(C=CC(=C1)C=CC(=O)OCC(CO)O)O 268.26 unknown https://doi.org/10.1016/0031-9422(91)85032-U
> Phenylpropanoids and polyketides / Cinnamic acids and derivatives / Hydroxycinnamic acids and derivatives / Hydroxycinnamic acid esters / Coumaric acid esters
2-Propenoic acid, 3-(4-hydroxyphenyl)-, 2,3-dihydroxypropyl ester, (E)- 5319874 Click to see C1=CC(=CC=C1C=CC(=O)OCC(CO)O)O 238.24 unknown https://doi.org/10.1016/0031-9422(91)85032-U
> 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/10.1016/0031-9422(91)85032-U
Ferulic acid 445858 Click to see COC1=C(C=CC(=C1)C=CC(=O)O)O 194.18 unknown https://doi.org/10.1016/0031-9422(91)85032-U
Isoferulic acid 736186 Click to see COC1=C(C=C(C=C1)C=CC(=O)O)O 194.18 unknown https://doi.org/10.1016/0031-9422(91)85032-U
p-Coumaric acid 637542 Click to see C1=CC(=CC=C1C=CC(=O)O)O 164.16 unknown https://doi.org/10.1016/0031-9422(91)85032-U

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