Salix cheilophila

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Synonyms

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Scientific Literature

Phytochemical Profile

Biological Material

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Details Top

Internal ID	UUID64404db5a64c0086694467
Scientific name	Salix cheilophila
Authority	C.K.Schneid.
First published in	Pl. Wilson. (Sargent) 3(1): 69. 1916 [8 May 1916]

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Synonyms Top

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Common names Top

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Filter by language:

Language	Common/alternative name
Chinese	乌柳
Chinese	筐柳
Chinese	沙柳
Chinese	烏柳

Subspecies (abbr. subsp./ssp.) Top

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Varieties (abbr. var.) Top

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Name	Authority	First published in
Salix cheilophila var. microstachyoides	(Z.Wang & P.Y.Fu) Z.Wang & C.F.Fang	Fl. Reipubl. Popularis Sin. 20(2): 355 (1984):.

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 click to expand
- China
  - China North-central
  - China South-central
  - Inner Mongolia
  - Tibet

Links to other databases Top

Suggest others/fix!

Database	ID/link to page
World Flora Online	wfo-0001134224
Tropicos	28301614
KEW	urn:lsid:ipni.org:names:777297-1
The Plant List	tro-28301614
Open Tree Of Life	1022766
NCBI Taxonomy	688336
IPNI	777297-1
GBIF	7266613
Wikipedia	Salix_cheilophila

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

Patterns and environmental drivers of C, N, and P stoichiometry in the leaf‐litter‐soil system associated with Mongolian pine forests

Ren Y, Gao G, Ding G, Zhang Y, Zhao P

Ecol Evol

20-Mar-2024

PMCID:	PMC10954427
doi:	10.1002/ece3.11172
PMID:	38516573

Biogeographic distribution of autotrophic bacteria was more affected by precipitation than by soil properties in an arid area

Wang Y, Huang Y, Zeng Q, Liu D, An S

Front Microbiol

20-Dec-2023

PMCID:	PMC10761425
doi:	10.3389/fmicb.2023.1303469
PMID:	38173682

Indirect regulation of topsoil nutrient cycling by groundwater depth: impacts on sand-fixing vegetation and rhizosphere bacterial communities

Hao L, Liu X, Ji R, Ma Y, Wu P, Cao Q, Xin Y

Front Microbiol

05-Dec-2023

PMCID:	PMC10746847
doi:	10.3389/fmicb.2023.1285922
PMID:	38143862

Rodents Inhabiting the Southeastern Mu Us Desert May Not Have Experienced Prolonged Heat Stress in Summer 2022

Guo YY, Wang SS, Wang X, Liu W, Xu D

Animals (Basel)

26-Jun-2023

PMCID:	PMC10340019
doi:	10.3390/ani13132114
PMID:	37443912

Fine root dynamics and its contribution to soil organic carbon stocks with Caragana intermedia plantation development in alpine sandy land

Li Q, Jia Z, He L, Zhao X, Yang H

Front Plant Sci

09-Mar-2023

PMCID:	PMC10034096
doi:	10.3389/fpls.2023.1093678
PMID:	36968380

An ethnobiological study on traditional knowledge associated with black-boned sheep (Ovis aries) in Northwest Yunnan, China

Fan Y, Cheng Z, Liu B, Hu X, Ali M, Long C

J Ethnobiol Ethnomed

17-May-2022

PMCID:	PMC9112469
doi:	10.1186/s13002-022-00537-5
PMID:	35581643

Changes in soil carbon sequestration and emission in different succession stages of biological soil crusts in a sand-binding area

Wang B, Liu J, Zhang X, Wang C

Carbon Balance Manag

13-Sep-2021

PMCID:	PMC8439077
doi:	10.1186/s13021-021-00190-7
PMID:	34518908

Fine root dynamic characteristics and effect on plantation’s carbon sequestration of three Salix shrub plantations in Tibetan Plateau alpine sandy land

He L, Jia Z, Li Q, Zhang Y, Wu R, Dai J, Gao Y

Ecol Evol

02-Feb-2021

PMCID:	PMC7981207
doi:	10.1002/ece3.7221
PMID:	33767826

Fine‐root decomposition characteristics of four typical shrubs in sandy areas of an arid and semiarid alpine region in western China

He L, Jia Z, Li Q, Feng L, Yang K

Ecol Evol

12-Apr-2019

PMCID:	PMC6509441
doi:	10.1002/ece3.5133
PMID:	31110689

The Biogeographical Distribution of Soil Bacterial Communities in the Loess Plateau as Revealed by High-Throughput Sequencing

Liu D, Yang Y, An S, Wang H, Wang Y

Front Microbiol

18-Oct-2018

PMCID:	PMC6200921
doi:	10.3389/fmicb.2018.02456
PMID:	30405547

Dynamics of biomass and carbon sequestration across a chronosequence of Caragana intermedia plantations on alpine sandy land

Li Q, Jia Z, Feng L, He L, Yang K

Sci Rep

20-Aug-2018

PMCID:	PMC6102266
doi:	10.1038/s41598-018-30595-3
PMID:	30127413

Seasonal Dynamics of Water Use Strategy of Two Salix Shrubs in Alpine Sandy Land, Tibetan Plateau

Zhu Y, Wang G, Li R

PLoS One

31-May-2016

PMCID:	PMC4887004
doi:	10.1371/journal.pone.0156586
PMID:	27243772

Functional traits drive the contribution of solar radiation to leaf litter decomposition among multiple arid-zone species

Pan X, Song YB, Liu GF, Hu YK, Ye XH, Cornwell WK, Prinzing A, Dong M, Cornelissen JH

Sci Rep

18-Aug-2015

PMCID:	PMC4539537
doi:	10.1038/srep13217
PMID:	26282711

Spatial Heterogeneity of Soil Nutrients after the Establishment of Caragana intermedia Plantation on Sand Dunes in Alpine Sandy Land of the Tibet Plateau

Li Q, Jia Z, Zhu Y, Wang Y, Li H, Yang D, Zhao X

PLoS One

06-May-2015

PMCID:	PMC4422674
doi:	10.1371/journal.pone.0124456
PMID:	25946170

Acyclic Diterpene‐γ‐Lactones and Flavonoid from <i>Salix Cheilophila</i> Omitted

Tong Shen, Yong‐Qiang Tian, Wu‐Xia Liu, Shang‐Zhen Zheng

Wiley

01-May-2015

doi:	10.1002/JCCS.200800059

Phytochemical Profile Top

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Below are displayed the proven (via scientific papers) natural compounds!
You can also contribute to this by clicking here.

Name	PubChem ID	Canonical SMILES	MW	Found in	Proof
> Lipids and lipid-like molecules / Prenol lipids / Terpene lactones / Diterpene lactones
[(2Z,6E,10E)-10-[(4S,5R)-4-hydroxy-5-(2-methylprop-1-enyl)-2-oxooxolan-3-ylidene]-3,7-dimethyldeca-2,6-dienyl] (3S)-3-hydroxybutanoate	162944094	Click to see CC(CC(=O)OCC=C(C)CCC=C(C)CCC=C1C(C(OC1=O)C=C(C)C)O)O	420.50	unknown	https://doi.org/10.1002/JCCS.200800059
[(2Z,6E,10E)-10-[(4S,5R)-4-hydroxy-5-(2-methylprop-1-enyl)-2-oxooxolan-3-ylidene]-3,7-dimethyldeca-2,6-dienyl] (E)-3-methylpent-2-enoate	162912204	Click to see CCC(=CC(=O)OCC=C(C)CCC=C(C)CCC=C1C(C(OC1=O)C=C(C)C)O)C	430.60	unknown	https://doi.org/10.1002/JCCS.200800059
[(2Z,6E,8S,10E)-8-acetyloxy-10-[(4S,5R)-4-hydroxy-5-(2-methylprop-1-enyl)-2-oxooxolan-3-ylidene]-3,7-dimethyldeca-2,6-dienyl] (E)-3-methylpent-2-enoate	162900495	Click to see CCC(=CC(=O)OCC=C(C)CCC=C(C)C(CC=C1C(C(OC1=O)C=C(C)C)O)OC(=O)C)C	488.60	unknown	https://doi.org/10.1002/JCCS.200800059
[(2Z,6E,8S,10E)-8-acetyloxy-10-[(4S,5R)-4-hydroxy-5-(2-methylprop-1-enyl)-2-oxooxolan-3-ylidene]-3,7-dimethyldeca-2,6-dienyl] (Z)-2-methylbut-2-enoate	162931236	Click to see CC=C(C)C(=O)OCC=C(C)CCC=C(C)C(CC=C1C(C(OC1=O)C=C(C)C)O)OC(=O)C	474.60	unknown	https://doi.org/10.1002/JCCS.200800059
[10-[4-Hydroxy-5-(2-methylprop-1-enyl)-2-oxooxolan-3-ylidene]-3,7-dimethyldeca-2,6-dienyl] 3-hydroxybutanoate	162944093	Click to see CC(CC(=O)OCC=C(C)CCC=C(C)CCC=C1C(C(OC1=O)C=C(C)C)O)O	420.50	unknown	https://doi.org/10.1002/JCCS.200800059
[10-[4-Hydroxy-5-(2-methylprop-1-enyl)-2-oxooxolan-3-ylidene]-3,7-dimethyldeca-2,6-dienyl] 3-methylpent-2-enoate	162912203	Click to see CCC(=CC(=O)OCC=C(C)CCC=C(C)CCC=C1C(C(OC1=O)C=C(C)C)O)C	430.60	unknown	https://doi.org/10.1002/JCCS.200800059
[8-Acetyloxy-10-[4-hydroxy-5-(2-methylprop-1-enyl)-2-oxooxolan-3-ylidene]-3,7-dimethyldeca-2,6-dienyl] 2-methylbut-2-enoate	162931235	Click to see CC=C(C)C(=O)OCC=C(C)CCC=C(C)C(CC=C1C(C(OC1=O)C=C(C)C)O)OC(=O)C	474.60	unknown	https://doi.org/10.1002/JCCS.200800059
[8-Acetyloxy-10-[4-hydroxy-5-(2-methylprop-1-enyl)-2-oxooxolan-3-ylidene]-3,7-dimethyldeca-2,6-dienyl] 3-methylpent-2-enoate	162900494	Click to see CCC(=CC(=O)OCC=C(C)CCC=C(C)C(CC=C1C(C(OC1=O)C=C(C)C)O)OC(=O)C)C	488.60	unknown	https://doi.org/10.1002/JCCS.200800059
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Bile acids, alcohols and derivatives / Hydroxy bile acids, alcohols and derivatives / Tetrahydroxy bile acids, alcohols and derivatives
[(2S,3R,5S,9R,10R,13R,14S,17S)-17-[(2R,3R)-2,3-dihydroxy-6-methyl-5-methylideneheptan-2-yl]-3,14-dihydroxy-10,13-dimethyl-6-oxo-2,3,4,5,9,11,12,15,16,17-decahydro-1H-cyclopenta[a]phenanthren-2-yl] acetate	162895620	Click to see CC(C)C(=C)CC(C(C)(C1CCC2(C1(CCC3C2=CC(=O)C4C3(CC(C(C4)O)OC(=O)C)C)C)O)O)O	518.70	unknown	https://doi.org/10.1002/JCCS.200800059
[17-(2,3-dihydroxy-6-methyl-5-methylideneheptan-2-yl)-3,14-dihydroxy-10,13-dimethyl-6-oxo-2,3,4,5,9,11,12,15,16,17-decahydro-1H-cyclopenta[a]phenanthren-2-yl] acetate	162895619	Click to see CC(C)C(=C)CC(C(C)(C1CCC2(C1(CCC3C2=CC(=O)C4C3(CC(C(C4)O)OC(=O)C)C)C)O)O)O	518.70	unknown	https://doi.org/10.1002/JCCS.200800059
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Hydroxysteroids
(1S,4aS,4bR,7S,8aR,10aR)-7-ethyl-8a-hydroxy-1-(hydroxymethyl)-1,4a,7-trimethyl-4,4b,5,6,8,9,10,10a-octahydro-3H-phenanthren-2-one	162945922	Click to see CCC1(CCC2C3(CCC(=O)C(C3CCC2(C1)O)(C)CO)C)C	322.50	unknown	https://doi.org/10.1002/JCCS.200800059
7-ethyl-8a-hydroxy-1-(hydroxymethyl)-1,4a,7-trimethyl-4,4b,5,6,8,9,10,10a-octahydro-3H-phenanthren-2-one	162945921	Click to see CCC1(CCC2C3(CCC(=O)C(C3CCC2(C1)O)(C)CO)C)C	322.50	unknown	https://doi.org/10.1002/JCCS.200800059
> 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/10.1002/JCCS.200800059
17-(5-Ethyl-6-methylheptan-2-yl)-3-hydroxy-10,13-dimethyl-1,2,3,7,8,9,11,12,14,15,16,17-dodecahydrocyclopenta[a]phenanthren-6-one	14804218	Click to see CCC(CCC(C)C1CCC2C1(CCC3C2CC(=O)C4=CC(CCC34C)O)C)C(C)C	428.70	unknown	https://doi.org/10.1002/JCCS.200800059
3-Hydroxystigmast-5-en-7-one	160608	Click to see CCC(CCC(C)C1CCC2C1(CCC3C2C(=O)C=C4C3(CCC(C4)O)C)C)C(C)C	428.70	unknown	https://doi.org/10.1002/JCCS.200800059
3beta-Hydroxyporiferast-5-en-7-one	14779505	Click to see CCC(CCC(C)C1CCC2C1(CCC3C2C(=O)C=C4C3(CCC(C4)O)C)C)C(C)C	428.70	unknown	https://doi.org/10.1002/JCCS.200800059
3beta-Hydroxystigmast-4-en-6-one	10982859	Click to see CCC(CCC(C)C1CCC2C1(CCC3C2CC(=O)C4=CC(CCC34C)O)C)C(C)C	428.70	unknown	https://doi.org/10.1002/JCCS.200800059
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/10.1002/JCCS.200800059
> Phenylpropanoids and polyketides / Cinnamic acids and derivatives / Hydroxycinnamic acids and derivatives / Hydroxycinnamic acid esters / Hydroxycinnamic acid glycosides
[3,4,5-Trihydroxy-6-(hydroxymethyl)oxan-2-yl] 3-(4-hydroxy-3-methoxyphenyl)prop-2-enoate	72983454	Click to see COC1=C(C=CC(=C1)C=CC(=O)OC2C(C(C(C(O2)CO)O)O)O)O	356.32	unknown	https://doi.org/10.1002/JCCS.200800059
1-O-feruloyl-beta-D-glucose	13962928	Click to see COC1=C(C=CC(=C1)C=CC(=O)OC2C(C(C(C(O2)CO)O)O)O)O	356.32	unknown	https://doi.org/10.1002/JCCS.200800059
> 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	https://doi.org/10.1002/JCCS.200800059
Caffeic Acid	689043	Click to see C1=CC(=C(C=C1C=CC(=O)O)O)O	180.16	unknown	https://doi.org/10.1002/JCCS.200800059
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid O-glycosides
7-hydroxy-2-(7-methoxy-1,3-benzodioxol-5-yl)-6-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxychromen-4-one	162848384	Click to see COC1=CC(=CC2=C1OCO2)C3=CC(=O)C4=CC(=C(C=C4O3)O)OC5C(C(C(C(O5)CO)O)O)O	490.40	unknown	https://doi.org/10.1002/JCCS.200800059
7-Hydroxy-2-(7-methoxy-1,3-benzodioxol-5-yl)-6-[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxychromen-4-one	162848383	Click to see COC1=CC(=CC2=C1OCO2)C3=CC(=O)C4=CC(=C(C=C4O3)O)OC5C(C(C(C(O5)CO)O)O)O	490.40	unknown	https://doi.org/10.1002/JCCS.200800059
Luteolin 5-glucoside	5317471	Click to see C1=CC(=C(C=C1C2=CC(=O)C3=C(O2)C=C(C=C3OC4C(C(C(C(O4)CO)O)O)O)O)O)O	448.40	unknown	https://doi.org/10.1002/JCCS.200800059
Luteolin-5-O-b-D-glucopyranoside	15559460	Click to see C1=CC(=C(C=C1C2=CC(=O)C3=C(O2)C=C(C=C3OC4C(C(C(C(O4)CO)O)O)O)O)O)O	448.40	unknown	https://doi.org/10.1002/JCCS.200800059
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid O-glycosides / Flavonoid-7-O-glycosides
[2-Hydroxy-4-[5-hydroxy-4-oxo-7-[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxychromen-2-yl]phenyl] 2-methylbut-2-enoate	74977679	Click to see CC=C(C)C(=O)OC1=C(C=C(C=C1)C2=CC(=O)C3=C(C=C(C=C3O2)OC4C(C(C(C(O4)CO)O)O)O)O)O	530.50	unknown	https://doi.org/10.1002/JCCS.200800059
Luteolin 7-galactoside	5291488	Click to see C1=CC(=C(C=C1C2=CC(=O)C3=C(C=C(C=C3O2)OC4C(C(C(C(O4)CO)O)O)O)O)O)O	448.40	unknown	https://doi.org/10.1002/JCCS.200800059
luteolin 7-O-beta-D-glucoside-4'-(Z-2-methyl-2-butenoate)	91666353	Click to see CC=C(C)C(=O)OC1=C(C=C(C=C1)C2=CC(=O)C3=C(C=C(C=C3O2)OC4C(C(C(C(O4)CO)O)O)O)O)O	530.50	unknown	https://doi.org/10.1002/JCCS.200800059
Luteolin 7-O-glucoside	5280637	Click to see C1=CC(=C(C=C1C2=CC(=O)C3=C(C=C(C=C3O2)OC4C(C(C(C(O4)CO)O)O)O)O)O)O	448.40	unknown	https://doi.org/10.1002/JCCS.200800059
> Phenylpropanoids and polyketides / Flavonoids / O-methylated flavonoids / 3-O-methylated flavonoids
6,7-Dihydroxy-2-(7-methoxy-1,3-benzodioxol-5-yl)chromen-4-one	162938894	Click to see COC1=CC(=CC2=C1OCO2)C3=CC(=O)C4=CC(=C(C=C4O3)O)O	328.27	unknown	https://doi.org/10.1002/JCCS.200800059

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Salix cheilophila

Table of Contents

Details Top

Description Top

Synonyms Top

Common names Top

Subspecies (abbr. subsp./ssp.) Top

Varieties (abbr. var.) Top

Subvarieties (abbr. subvar.) Top

Forms (abbr. f.) Top

Germination/Propagation Top

Distribution (via POWO/KEW) Top

Links to other databases Top

Genomes (via NCBI) Top

Scientific Literature Top

Phytochemical Profile Top

Biological Material Top

Contributors Top

Collections Top