Populus tomentosa - Unknown
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Internal ID UUID64404d9b9d2c1616685004
Scientific name Populus tomentosa
Authority Carrière
First published in Rev. Hort. (Paris) 39: 340 (1867)

Description Top

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Populus × tomentosa, also known as Chinese white poplar or Peking poplar, is a species of tree in the Salicaceae family. It is native to northern and eastern China and has been introduced to Louisiana in the United States. This large tree is known for its strong resistance to diseases and insects, making it a popular choice for shelterbelts and urban afforestation in northern China. While it is believed to be a hybrid, the exact parent species of Populus × tomentosa are still unknown. It is also notable for its fibrous roots, which are more abundant compared to other trees. This species can be found in a wide range of elevations, from sea level to 1,500 meters in China.

Synonyms Top

No known synonyms.

Common names Top

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Language Common/alternative name
English chinese white poplar
Arabic حور لبدي
Turkish Çin ak kavağı
Chinese 毛白杨
Chinese 响杨
Chinese 大叶杨
Chinese 杨树花
Chinese 杨枸花
Chinese 毛白楊
Chinese 白杨

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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Distribution (via POWO/KEW) Top

Legend for the distribution data:
- Doubtful data
- Extinct
- Introduced
- Native
  • Asia-temperate
    • China
      • China North-central
      • China South-central
      • China Southeast
      • Inner Mongolia
      • Manchuria

Links to other databases Top

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Database ID/link to page
World Flora Online wfo-0001133621
USDA Plants POTO7
Tropicos 28300546
KEW urn:lsid:ipni.org:names:776882-1
The Plant List kew-5000215
Open Tree Of Life 61097
NCBI Taxonomy 118781
Nature Serve 2.138220
IPNI 776882-1
iNaturalist 167296
GBIF 3040195
EPPO POPTO
EOL 483052
USDA GRIN 29421
Wikipedia Populus_%C3%97_tomentosa
CMAUP NPO19792

Genomes (via NCBI) Top

Below is displayed the reference genome only!
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Accession Assembly
Name Level Submitter Released Coverage Size
GCA_018804465.1 PTv2 Chromosome Ori-Gene Co. Ltd. 2021-06-09 75.0x 704.57 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
Pest categorisation of Eulecanium giganteum Bragard C, Baptista P, Chatzivassiliou E, Di Serio F, Gonthier P, Jaques Miret JA, Justesen AF, Magnusson CS, Milonas P, Navas‐Cortes JA, Parnell S, Potting R, Reignault PL, Stefani E, Thulke H, Van der Werf W, Vicent Civera A, Yuen J, Zappalà L, Grégoire J, Malumphy C, Akrivou A, Kertesz V, Papachristos D, Sfyra O, MacLeod A EFSA J 03-Apr-2024
PMCID:PMC10988561
doi:10.2903/j.efsa.2024.8666
PMID:38576539
Identification and functional analysis of the LEAFY gene in longan flower induction Jue D, Li Z, Zhang W, Tang J, Xie T, Sang X, Guo Q BMC Genomics 25-Mar-2024
PMCID:PMC10962150
doi:10.1186/s12864-024-10229-x
PMID:38528464
OsmiR319-OsPCF5 modulate resistance to brown planthopper in rice through association with MYB proteins Sun B, Shen Y, Zhu L, Yang X, Liu X, Li D, Zhu M, Miao X, Shi Z BMC Biol 22-Mar-2024
PMCID:PMC10960409
doi:10.1186/s12915-024-01868-3
PMID:38520013
Green solution to riparian pollution: Populus alba L. potential for phytoremediation and bioindication of PTEs along the Sava river Miletić Z, Jonjev M, Jarić S, Kostić O, Sekulić D, Mitrović M, Pavlović P Heliyon 18-Mar-2024
PMCID:PMC10981065
doi:10.1016/j.heliyon.2024.e28183
PMID:38560157
CRISPR/Cas9 –based genome editing to expedite the genetic improvement of palms: challenges and prospects Ramesh S, Rajesh M, Das A, Hebbar K Front Plant Sci 13-Mar-2024
PMCID:PMC10965634
doi:10.3389/fpls.2024.1385037
PMID:38545392
Investigation of two-pore K+ (TPK) channels in Triticum aestivum L. suggests their role in stress response Kaur A, Madhu, Sharma A, Singh K, Upadhyay SK Heliyon 13-Mar-2024
PMCID:PMC10963239
doi:10.1016/j.heliyon.2024.e27814
PMID:38533012
Transcriptional regulation of flavonol biosynthesis in plants Cao Y, Mei Y, Zhang R, Zhong Z, Yang X, Xu C, Chen K, Li X Hortic Res 15-Feb-2024
PMCID:PMC11017525
doi:10.1093/hr/uhae043
PMID:38623072
Genome-Wide Identification and Characterization of Tomato Fatty Acid β-Oxidase Family Genes KAT and MFP Li L, Liu Z, Pan X, Yao K, Wang Y, Yang T, Huang G, Liao W, Wang C Int J Mol Sci 14-Feb-2024
PMCID:PMC10889323
doi:10.3390/ijms25042273
PMID:38396949
The Potential Role of Genic-SSRs in Driving Ecological Adaptation Diversity in Caragana Plants Wang Q, Chen X, Meng Y, Niu M, Jia Y, Huang L, Ma W, Liang C, Li Z, Zhao L, Dang Z Int J Mol Sci 08-Feb-2024
PMCID:PMC10888960
doi:10.3390/ijms25042084
PMID:38396759
Genome-wide identification and characterization of NAC transcription factor family members in Trifolium pratense and expression analysis under lead stress Wang Z, Chen Z, Wu Y, Mu M, Jiang J, Nie W, Zhao S, Cui G, Yin X BMC Genomics 31-Jan-2024
PMCID:PMC10829316
doi:10.1186/s12864-023-09944-8
PMID:38297198
Proteomic and Metabolomic Analysis of the Quercus ilex–Phytophthora cinnamomi Pathosystem Reveals a Population-Specific Response, Independent of Co-Occurrence of Drought Hernández-Lao T, Tienda-Parrilla M, Labella-Ortega M, Guerrero-Sánchez VM, Rey MD, Jorrín-Novo JV, Castillejo-Sánchez MÁ Biomolecules 29-Jan-2024
PMCID:PMC10887186
doi:10.3390/biom14020160
PMID:38397397
Identification and Expression Patterns of WOX Transcription Factors under Abiotic Stresses in Pinus massoniana Wang D, Qiu Z, Xu T, Yao S, Zhang M, Cheng X, Zhao Y, Ji K Int J Mol Sci 28-Jan-2024
PMCID:PMC10855728
doi:10.3390/ijms25031627
PMID:38338907
Characterization and analysis of multi-organ full-length transcriptomes in Sphaeropteris brunoniana and Alsophila latebrosa highlight secondary metabolism and chloroplast RNA editing pattern of tree ferns Peng Y, Wang Z, Li M, Wang T, Su Y BMC Plant Biol 26-Jan-2024
PMCID:PMC10811885
doi:10.1186/s12870-024-04746-w
PMID:38273309
PtoMYB031, the R2R3 MYB transcription factor involved in secondary cell wall biosynthesis in poplar Tang F, Jiao B, Zhang M, He M, Su R, Luo K, Lan T Front Plant Sci 17-Jan-2024
PMCID:PMC10828011
doi:10.3389/fpls.2023.1341245
PMID:38298604
Revealing the transitory and local effect of zebularine on development and on proteome dynamics of Salix purpurea Pagano A, Gomes C, Timmerman E, Sulima P, Przyborowski JA, Kruszka D, Impens F, Paiva JA Front Plant Sci 17-Jan-2024
PMCID:PMC10827895
doi:10.3389/fpls.2023.1304327
PMID:38298602

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 / Anthracenes / Anthraquinones
1-Hydroxy-2-methoxyanthraquinone 80103 Click to see COC1=C(C2=C(C=C1)C(=O)C3=CC=CC=C3C2=O)O 254.24 unknown via CMAUP database
1-Methoxy-2-methylanthracene-9,10-dione 3534338 Click to see CC1=C(C2=C(C=C1)C(=O)C3=CC=CC=C3C2=O)OC 252.26 unknown via CMAUP database
1,3-Dimethoxyanthraquinone 361511 Click to see COC1=CC2=C(C(=C1)OC)C(=O)C3=CC=CC=C3C2=O 268.26 unknown via CMAUP database
> Benzenoids / Anthracenes / Anthraquinones / Hydroxyanthraquinones
1,3-Dihydroxyanthraquinone 196978 Click to see C1=CC=C2C(=C1)C(=O)C3=C(C2=O)C(=CC(=C3)O)O 240.21 unknown via CMAUP database
2-Hydroxyanthraquinone 11796 Click to see C1=CC=C2C(=C1)C(=O)C3=C(C2=O)C=C(C=C3)O 224.21 unknown via CMAUP database
Alizarin 6293 Click to see C1=CC=C2C(=C1)C(=O)C3=C(C2=O)C(=C(C=C3)O)O 240.21 unknown via CMAUP database
Alizarin 1-methyl ether 80309 Click to see COC1=C(C=CC2=C1C(=O)C3=CC=CC=C3C2=O)O 254.24 unknown via CMAUP database
Lucidin 10163 Click to see C1=CC=C2C(=C1)C(=O)C3=CC(=C(C(=C3C2=O)O)CO)O 270.24 unknown via CMAUP database
Purpurin 6683 Click to see C1=CC=C2C(=C1)C(=O)C3=C(C2=O)C(=C(C=C3O)O)O 256.21 unknown via CMAUP database
Rubiadin 124062 Click to see CC1=C(C=C2C(=C1O)C(=O)C3=CC=CC=C3C2=O)O 254.24 unknown via CMAUP database
> Benzenoids / Benzene and substituted derivatives / Benzoic acids and derivatives / Aminobenzoic acids and derivatives / Aminobenzoic acids
2-((Carboxymethyl)amino)-4-chlorobenzoic acid 11107141 Click to see C1=CC(=C(C=C1Cl)NCC(=O)O)C(=O)O 229.62 unknown via CMAUP database
> Benzenoids / Benzene and substituted derivatives / Benzoic acids and derivatives / Hydroxybenzoic acid derivatives
4-Hydroxybenzoic acid 135 Click to see C1=CC(=CC=C1C(=O)O)O 138.12 unknown via CMAUP database
> Benzenoids / Benzene and substituted derivatives / Benzoic acids and derivatives / Hydroxybenzoic acid derivatives / Gallic acid and derivatives / Gallic acids
Gallic Acid 370 Click to see C1=C(C=C(C(=C1O)O)O)C(=O)O 170.12 unknown via CMAUP database
> Benzenoids / Benzene and substituted derivatives / Phenylmethylamines
2-(Aminomethyl)phenol 70267 Click to see C1=CC=C(C(=C1)CN)O 123.15 unknown via CMAUP database
> Benzenoids / Naphthalenes / Naphthols and derivatives
4-Methoxy-1-naphthol 66542 Click to see COC1=CC=C(C2=CC=CC=C21)O 174.20 unknown via CMAUP database
> Benzenoids / Phenols / Methoxyphenols
Vanillin 1183 Click to see COC1=C(C=CC(=C1)C=O)O 152.15 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Terpene glycosides / Iridoid O-glycosides
Monotropein 73466 Click to see C1=CC(C2C1C(=COC2OC3C(C(C(C(O3)CO)O)O)O)C(=O)O)(CO)O 390.34 unknown via CMAUP database
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Stigmastanes and derivatives
(3R,4S,5S,6R)-2-[[(3S,8S,9S,10R,13R,14S)-17-[(2R,5R)-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-yl]oxy]-6-(hydroxymethyl)oxane-3,4,5-triol 52940117 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 / O-glycosyl compounds
Asperuloside 84298 Click to see CC(=O)OCC1=CC2C3C1C(OC=C3C(=O)O2)OC4C(C(C(C(O4)CO)O)O)O 414.40 unknown via CMAUP database
D-Alt(a1-2a)L-Psif 53301851 Click to see C(C1C(C(C(C(O1)OC2(C(C(C(O2)CO)O)O)CO)O)O)O)O 342.30 unknown via CMAUP database
> Organic oxygen compounds / Organooxygen compounds / Carbohydrates and carbohydrate conjugates / Glycosyl compounds / Phenolic glycosides
(2S,3S,4R,5R,6S)-2-(hydroxymethyl)-6-[2-(hydroxymethyl)phenoxy]oxane-3,4,5-triol 6931410 Click to see C1=CC=C(C(=C1)CO)OC2C(C(C(C(O2)CO)O)O)O 286.28 unknown via CMAUP database
[3,4,5-Trihydroxy-6-[2-(hydroxymethyl)phenoxy]oxan-2-yl]methyl benzoate 278591 Click to see C1=CC=C(C=C1)C(=O)OCC2C(C(C(C(O2)OC3=CC=CC=C3CO)O)O)O 390.40 unknown via CMAUP database
[4,5-Dihydroxy-6-(hydroxymethyl)-2-[2-(hydroxymethyl)phenoxy]oxan-3-yl] benzoate 12444467 Click to see C1=CC=C(C=C1)C(=O)OC2C(C(C(OC2OC3=CC=CC=C3CO)CO)O)O 390.40 unknown via CMAUP database
Salireposide 117440 Click to see C1=CC=C(C=C1)C(=O)OCC2=C(C=CC(=C2)O)OC3C(C(C(C(O3)CO)O)O)O 406.40 unknown via CMAUP database
Siebolside B 16083169 Click to see C1=CC=C(C=C1)C(=O)OCC2=CC(=C(C=C2)O)OC3C(C(C(C(O3)CO)O)O)O 406.40 unknown via CMAUP database
Tremulacin 442544 Click to see C1CC(=O)C(C=C1)(C(=O)OCC2=CC=CC=C2OC3C(C(C(C(O3)CO)O)O)OC(=O)C4=CC=CC=C4)O 528.50 unknown https://doi.org/10.1016/S0944-7113(11)80067-X
> Phenylpropanoids and polyketides / Cinnamic acids and derivatives / Hydroxycinnamic acids and derivatives / Hydroxycinnamic acids
(E)-3-(3,4-dihydroxyphenyl)prop-2-enoic acid 2518 Click to see C1=CC(=C(C=C1C=CC(=O)O)O)O 180.16 unknown via CMAUP database
4-Hydroxycinnamic acid 322 Click to see C1=CC(=CC=C1C=CC(=O)O)O 164.16 unknown via CMAUP database
> Phenylpropanoids and polyketides / Coumarins and derivatives
Coumarin 323 Click to see C1=CC=C2C(=C1)C=CC(=O)O2 146.14 unknown via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavones
7-Hydroxy-4-oxo-2-phenylchromen-5-olate 25200543 Click to see C1=CC=C(C=C1)C2=CC(=O)C3=C(C=C(C=C3O2)O)[O-] 253.23 unknown via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavones / Flavonols
Rhamnocitrin 5320946 Click to see COC1=CC(=C2C(=C1)OC(=C(C2=O)O)C3=CC=C(C=C3)O)O 300.26 unknown via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid O-glycosides
2-(4-Hydroxyphenyl)-7-methoxy-5-[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-2,3-dihydrochromen-4-one 348162 Click to see COC1=CC2=C(C(=O)CC(O2)C3=CC=C(C=C3)O)C(=C1)OC4C(C(C(C(O4)CO)O)O)O 448.40 unknown via CMAUP database
Sakuranin 73607 Click to see COC1=CC2=C(C(=O)CC(O2)C3=CC=C(C=C3)O)C(=C1)OC4C(C(C(C(O4)CO)O)O)O 448.40 unknown via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid O-glycosides / Flavonoid-7-O-glycosides
Echinacin 6439941 Click to see C1=CC(=CC=C1C=CC(=O)OCC2C(C(C(C(O2)OC3=CC(=C4C(=C3)OC(=CC4=O)C5=CC=C(C=C5)O)O)O)O)O)O 578.50 unknown via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / O-methylated flavonoids / 3-O-methylated flavonoids
Tricin 5281702 Click to see COC1=CC(=CC(=C1O)OC)C2=CC(=O)C3=C(C=C(C=C3O2)O)O 330.29 unknown via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / O-methylated flavonoids / 7-O-methylated flavonoids
(2R)-5-hydroxy-2-(4-hydroxyphenyl)-7-methoxy-2,3-dihydrochromen-4-one 821416 Click to see COC1=CC(=C2C(=O)CC(OC2=C1)C3=CC=C(C=C3)O)O 286.28 unknown via CMAUP database
5-Hydroxy-7-methoxy-2-phenylchroman-4-one 73201 Click to see COC1=CC(=C2C(=O)CC(OC2=C1)C3=CC=CC=C3)O 270.28 unknown https://doi.org/10.1016/0305-1978(91)90071-7
Pinostrobin 6950539 Click to see COC1=CC(=C2C(=O)CC(OC2=C1)C3=CC=CC=C3)O 270.28 unknown https://doi.org/10.1016/0305-1978(91)90071-7

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