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Pinus elliottii

Pinus elliottii - Unknown
Part: Unknown
Author: Public Domain - WikiMedia
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Table of Contents

Details
Description
Synonyms
Common Names
Subtypes (subspecies, varieties, subvarieties, forms)
Germination/Propagation
Distribution
Links to other databases
Genome
Scientific Literature
Phytochemical Profile
Biological Material
Contributors
Collections

Details Top

Internal ID UUID64400223581d4885086906
Scientific name Pinus elliottii
Authority Engelm.
First published in Trans. Acad. Sci. St. Louis 4: 186 (1880)

Description Top

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No description added yet. Help us by writing one.

Synonyms Top

Scientific name Authority First published in
Pinus heterophylla Sudw. Bull. Torrey Bot. Club 20(2): 45. 1893 [15 Feb 1893]

Common names Top

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Language Common/alternative name
English slash pine
Spanish pino elioti
Afrikaans basden
Arabic صنوبر إليوتي
Bulgarian бор на Елиът
Czech borovice elliottova
Esperanto eliot-pino
Esperanto eo
Estonian elliotti mänd
Persian کاج باتلاقی
French pin à aiguilles longues
French pin d'elliott
Hebrew אורן אליוטי
Igbo slash pine
Icelandic flæðafura
Japanese スラッシュマツ
Lithuanian rantytoji pušis
Polish sosna elliotta
Russian Сосна Эллиота
Russian Сосна болотистая
Russian cосна Эллиота
udm Эллиотт пужым
Chinese 濕地松
Chinese 湿地松

Subspecies (abbr. subsp./ssp.) Top

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No subspecies added yet.

Varieties (abbr. var.) Top

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Name Authority First published in
Pinus elliottii var. densa Little & K.W.Dorman J. Forest. (Washington) 50: 921, figs. 1952
Pinus elliottii var. elliottii

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
  • Africa
    • Southern Africa
      • Free State
    • Western Indian Ocean
      • Mauritius
  • Northern America
    • Southeastern U.S.A.
      • Alabama
      • Florida
      • Georgia
      • Louisiana
      • Mississippi
      • South Carolina
  • Pacific
    • North-central Pacific
      • Hawaii
    • Southwestern Pacific
      • New Caledonia

Links to other databases Top

Suggest others/fix!
Database ID/link to page
World Flora Online wfo-0000481442
UNII 082P1K72IB
Florida Plant Atlas 3239
Flora of Alabama 211
USDA Plants PIEL
Tropicos 24900134
INPN 454239
KEW urn:lsid:ipni.org:names:262921-1
The Plant List kew-2562078
Open Tree Of Life 245809
NCBI Taxonomy 42064
Nature Serve 2.148214
IUCN Red List 42361
IPNI 262921-1
iNaturalist 69985
GBIF 5285777
Freebase /m/02jy19
FEIS plants/tree/pinell
EPPO PIUEL
EOL 1061757
Calflora (Californian flora) 9382
US Library of Congress sh86007150
USDA GRIN 28447
Wikipedia Pinus_elliottii
CMAUP NPO21240
PaleoBotany 48052

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
Climate change could negate U.S. forest ecosystem service benefits gained through reductions in nitrogen and sulfur deposition Phelan JN, Van Houtven G, Clark CM, Buckley J, Cajka J, Hargrave A, Horn K, Thomas RQ, Sabo RD Sci Rep 10-May-2024
PMCID:PMC11087459
doi:10.1038/s41598-024-60652-z
PMID:38730011
Lead and copper removal from sterile dumps by phytoremediation with Robinia pseudoacacia Chirilă Băbău AM, Micle V, Damian GE, Sur IM Sci Rep 29-Apr-2024
PMCID:PMC11059218
doi:10.1038/s41598-024-60412-z
PMID:38684877
Synergistic variation of rhizosphere soil phosphorus availability and microbial diversity with stand age in plantations of the endangered tree species Parashorea chinensis Li W, Ullah S, Liu F, Deng F, Han X, Huang S, Xu Y, Yang M Front Plant Sci 12-Apr-2024
PMCID:PMC11045988
doi:10.3389/fpls.2024.1372634
PMID:38681220
Phytosulfokine alpha enhances regeneration of transformed and untransformed protoplasts of Brassica oleracea Vogrinčič V, Kastelec D, Murovec J Front Plant Sci 27-Mar-2024
PMCID:PMC11004253
doi:10.3389/fpls.2024.1379618
PMID:38601308
Pest categorisation of Pyrrhoderma noxium Bragard C, Baptista P, Chatzivassiliou E, Di Serio F, Gonthier P, Jaques Miret JA, Justesen AF, MacLeod A, Magnusson CS, Milonas P, Navas‐Cortes JA, Parnell S, Potting R, Stefani E, Thulke H, Van der Werf W, Vicent Civera A, Yuen J, Zappalà L, Golic D, Gobbi A, Maiorano A, Pautasso M, Reignault PL EFSA J 19-Mar-2024
PMCID:PMC10949325
doi:10.2903/j.efsa.2024.8667
PMID:38505477
Physiological responses to drought stress of three pine species and comparative transcriptome analysis of Pinus yunnanensis var. pygmaea Xiao F, Zhao Y, Wang X, Jian X, Yang Y BMC Genomics 16-Mar-2024
PMCID:PMC10944613
doi:10.1186/s12864-024-10205-5
PMID:38493093
Colonization of root endophytic fungus Serendipita indica improves drought tolerance of Pinus taeda seedlings by regulating metabolome and proteome Wu C, Yang Y, Wang Y, Zhang W, Sun H Front Microbiol 15-Mar-2024
PMCID:PMC10978793
doi:10.3389/fmicb.2024.1294833
PMID:38559354
Pest categorisation of Dendrolimus punctatus 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, Gobbi A, Kertesz V, Maiorano A, Sfyra O, MacLeod A EFSA J 05-Mar-2024
PMCID:PMC10912981
doi:10.2903/j.efsa.2024.8504
PMID:38444826
Antioxidant Activity of Essential Oils from Pinaceae Species Ancuceanu R, Anghel AI, Hovaneț MV, Ciobanu AM, Lascu BE, Dinu M Antioxidants (Basel) 26-Feb-2024
PMCID:PMC10967544
doi:10.3390/antiox13030286
PMID:38539820
New Alien Plant Taxa for Italy and Europe: An Update Musarella CM, Laface VL, Angiolini C, Bacchetta G, Bajona E, Banfi E, Barone G, Biscotti N, Bonsanto D, Calvia G, Cambria S, Capuano A, Caruso G, Crisafulli A, Del Guacchio E, Di Gristina E, Domina G, Fanfarillo E, Fascetti S, Fiaschi T, Galasso G, Mascia F, Mazzacuva G, Mei G, Minissale P, Motti R, Perrino EV, Picone RM, Pinzani L, Podda L, Potenza G, Rosati L, Stinca A, Tavilla G, Villano C, Wagensommer RP, Spampinato G Plants (Basel) 24-Feb-2024
PMCID:PMC10934091
doi:10.3390/plants13050620
PMID:38475466
Modeling wood product carbon flows in southern us pine plantations: implications for carbon storage Puls SJ, Cook RL, Baker JS, Rakestraw JL, Trlica A Carbon Balance Manag 21-Feb-2024
PMCID:PMC10882772
doi:10.1186/s13021-024-00254-4
PMID:38381217
High-density genetic linkage mapping in Sitka spruce advances the integration of genomic resources in conifers Tumas H, Ilska JJ, Gérardi S, Laroche J, A’Hara S, Boyle B, Janes M, McLean P, Lopez G, Lee SJ, Cottrell J, Gorjanc G, Bousquet J, Woolliams JA, MacKay JJ G3 (Bethesda) 15-Feb-2024
PMCID:PMC10989875
doi:10.1093/g3journal/jkae020
PMID:38366548
Effects of continuous monoculture on rhizosphere soil nutrients, growth, physiological characteristics, hormone metabolome of Casuarina equisetifolia and their interaction analysis Wang Y, Wang Y, Li J, Cai Y, Hu M, Lin W, Wu Z Heliyon 13-Feb-2024
PMCID:PMC10878944
doi:10.1016/j.heliyon.2024.e26078
PMID:38384578
Limonene Enantiomeric Ratios from Anthropogenic and Biogenic Emission Sources Gu S, Luo W, Charmchi A, McWhirter KJ, Rosenstiel T, Pankow J, Faiola CL Environ Sci Technol Lett 02-Feb-2024
PMCID:PMC10867824
doi:10.1021/acs.estlett.3c00794
PMID:38371653
Anti-Leishmania major activity of Calotropis procera extract by increasing ROS production and upregulating TNF-α, IFN-γ and iNOS mRNA expression under in vitro conditions Amani S, Alinejad S, Asadi N, Yousefi E, Khademvatan S, Howarth GS Trop Med Health 01-Feb-2024
PMCID:PMC10832188
doi:10.1186/s41182-024-00578-4
PMID:38303082

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
> Benzenoids / Anthracenes / Anthraquinones / Hydroxyanthraquinones
Alterporriol N 57332378 Click to see CC1(C(CC2=C(C1O)C(=O)C3=C(C2=O)C(=CC(=C3C4=C(C=C(C5=C4C(=O)C6=C(C5=O)CC(C(C6O)(C)O)O)O)OC)OC)O)O)O 638.60 unknown https://doi.org/10.1016/S0031-9422(00)97394-1
> Lipids and lipid-like molecules / Fatty Acyls / Fatty acids and conjugates / Long-chain fatty acids
Oleic Acid 445639 Click to see CCCCCCCCC=CCCCCCCCC(=O)O 282.50 unknown via CMAUP database
Palmitic Acid 985 Click to see CCCCCCCCCCCCCCCC(=O)O 256.42 unknown via CMAUP database
Stearic Acid 5281 Click to see CCCCCCCCCCCCCCCCCC(=O)O 284.50 unknown via CMAUP database
> Lipids and lipid-like molecules / Fatty Acyls / Fatty acids and conjugates / Very long-chain fatty acids
Behenic Acid 8215 Click to see CCCCCCCCCCCCCCCCCCCCCC(=O)O 340.60 unknown via CMAUP database
> 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 via CMAUP database
Linolenic Acid 5280934 Click to see CCC=CCC=CCC=CCCCCCCCC(=O)O 278.40 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Diterpenoids
(13S)-15-Hydroxylabd-8(20)-en-19-oic acid methyl ester 101987389 Click to see CC(CCC1C(=C)CCC2C1(CCCC2(C)C(=O)OC)C)CCO 336.50 unknown https://doi.org/10.1016/S0031-9422(00)97394-1
methyl (1S,4aR,5S,8aR)-1,4a-dimethyl-6-methylidene-5-[(3R)-3-methyl-5-oxopentyl]-3,4,5,7,8,8a-hexahydro-2H-naphthalene-1-carboxylate 15602380 Click to see CC(CCC1C(=C)CCC2C1(CCCC2(C)C(=O)OC)C)CC=O 334.50 unknown https://doi.org/10.1016/S0031-9422(00)97394-1
methyl (1S,4aR,5S,8aR)-1,4a-dimethyl-6-methylidene-5-[(3S)-3-methyl-5-oxohexyl]-3,4,5,7,8,8a-hexahydro-2H-naphthalene-1-carboxylate 162887448 Click to see CC(CCC1C(=C)CCC2C1(CCCC2(C)C(=O)OC)C)CC(=O)C 348.50 unknown https://doi.org/10.1016/S0031-9422(00)97394-1
methyl (1S,4aR,5S,8aR)-1,4a-dimethyl-6-methylidene-5-[(3S)-3-methyl-5-oxopentyl]-3,4,5,7,8,8a-hexahydro-2H-naphthalene-1-carboxylate 162968952 Click to see CC(CCC1C(=C)CCC2C1(CCCC2(C)C(=O)OC)C)CC=O 334.50 unknown https://doi.org/10.1016/S0031-9422(00)97394-1
methyl (1S,4aR,5S,8aR)-5-(3,3-dimethyl-5-oxohexyl)-1,4a-dimethyl-6-methylidene-3,4,5,7,8,8a-hexahydro-2H-naphthalene-1-carboxylate 162949345 Click to see CC(=O)CC(C)(C)CCC1C(=C)CCC2C1(CCCC2(C)C(=O)OC)C 362.50 unknown https://doi.org/10.1016/S0031-9422(00)97394-1
methyl (1S,4aR,5S,8aS)-5-[(3S)-5-hydroxy-3-methylpentyl]-1,4a-dimethyl-6-methylidene-3,4,5,7,8,8a-hexahydro-2H-naphthalene-1-carboxylate 163002524 Click to see CC(CCC1C(=C)CCC2C1(CCCC2(C)C(=O)OC)C)CCO 336.50 unknown https://doi.org/10.1016/S0031-9422(00)97394-1
Methyl 1,4a-dimethyl-6-methylene-5-(3-methyl-5-oxohexyl)decahydro-1-naphthalenecarboxylate 578296 Click to see CC(CCC1C(=C)CCC2C1(CCCC2(C)C(=O)OC)C)CC(=O)C 348.50 unknown https://doi.org/10.1016/S0031-9422(00)97394-1
methyl 1,4a-dimethyl-6-methylidene-5-(3-methyl-5-oxopentyl)-3,4,5,7,8,8a-hexahydro-2H-naphthalene-1-carboxylate 15602378 Click to see CC(CCC1C(=C)CCC2C1(CCCC2(C)C(=O)OC)C)CC=O 334.50 unknown https://doi.org/10.1016/S0031-9422(00)97394-1
methyl 5-(3,3-dimethyl-5-oxohexyl)-1,4a-dimethyl-6-methylidene-3,4,5,7,8,8a-hexahydro-2H-naphthalene-1-carboxylate 162949344 Click to see CC(=O)CC(C)(C)CCC1C(=C)CCC2C1(CCCC2(C)C(=O)OC)C 362.50 unknown https://doi.org/10.1016/S0031-9422(00)97394-1
> Lipids and lipid-like molecules / Prenol lipids / Monoterpenoids / Bicyclic monoterpenoids
(-)-trans-Pinane 6429433 Click to see CC1CCC2CC1C2(C)C 138.25 unknown https://doi.org/10.1021/JF970075V
Pinane 10129 Click to see CC1CCC2CC1C2(C)C 138.25 unknown https://doi.org/10.1021/JF970075V
> Lipids and lipid-like molecules / Prenol lipids / Terpene glycosides / Triterpene glycosides / Triterpene saponins
(2S,3S,4S,5R,6R)-6-[[(3S,4aR,6aR,6bS,8aS,12aS,14aR,14bR)-8a-[(2S,3R,4S,5S,6R)-3-[(2S,3R,4S,5R,6S)-3,4-dihydroxy-6-methyl-5-[(2S,3R,4R,5R,6S)-3,4,5-trihydroxy-6-methyloxan-2-yl]oxyoxan-2-yl]oxy-4,5-dihydroxy-6-(hydroxymethyl)oxan-2-yl]oxycarbonyl-4,4,6a,6b,11,11,14b-heptamethyl-1,2,3,4a,5,6,7,8,9,10,12,12a,14,14a-tetradecahydropicen-3-yl]oxy]-5-[(2S,3R,4S,5R,6R)-4,5-dihydroxy-6-(hydroxymethyl)-3-[(2S,3R,4R,5R,6S)-3,4,5-trihydroxy-6-methyloxan-2-yl]oxyoxan-2-yl]oxy-3,4-dihydroxyoxane-2-carboxylic acid 21591284 Click to see CC1C(C(C(C(O1)OC2C(OC(C(C2O)O)OC3C(C(C(OC3OC(=O)C45CCC(CC4C6=CCC7C8(CCC(C(C8CCC7(C6(CC5)C)C)(C)C)OC9C(C(C(C(O9)C(=O)O)O)O)OC1C(C(C(C(O1)CO)O)O)OC1C(C(C(C(O1)C)O)O)O)C)(C)C)CO)O)O)C)O)O)O 1395.50 unknown via CMAUP database
(2S,3S,4S,5R,6R)-6-[[(3S,4S,4aR,6aR,6bS,8aS,12aS,14aR,14bR)-8a-[(2S,3R,4S,5S,6R)-3-[(2S,3R,4S,5R,6S)-3,4-dihydroxy-6-methyl-5-[(2S,3R,4R,5R,6S)-3,4,5-trihydroxy-6-methyloxan-2-yl]oxyoxan-2-yl]oxy-4,5-dihydroxy-6-(hydroxymethyl)oxan-2-yl]oxycarbonyl-4-(hydroxymethyl)-4,6a,6b,11,11,14b-hexamethyl-1,2,3,4a,5,6,7,8,9,10,12,12a,14,14a-tetradecahydropicen-3-yl]oxy]-5-[(2S,3R,4S,5R,6R)-4,5-dihydroxy-6-(hydroxymethyl)-3-[(2S,3R,4R,5R,6S)-3,4,5-trihydroxy-6-methyloxan-2-yl]oxyoxan-2-yl]oxy-3,4-dihydroxyoxane-2-carboxylic acid 21591283 Click to see CC1C(C(C(C(O1)OC2C(OC(C(C2O)O)OC3C(C(C(OC3OC(=O)C45CCC(CC4C6=CCC7C8(CCC(C(C8CCC7(C6(CC5)C)C)(C)CO)OC9C(C(C(C(O9)C(=O)O)O)O)OC1C(C(C(C(O1)CO)O)O)OC1C(C(C(C(O1)C)O)O)O)C)(C)C)CO)O)O)C)O)O)O 1411.50 unknown via CMAUP database
(3beta,4beta)-28-[[2-O-(6-Deoxy-alpha-L-mannopyranosyl)-beta-D-glucopyranosyl]oxy]-23-hydroxy-28-oxoolean-12-en-3-yl O-6-deoxy-alpha-L-mannopyranosyl-(1-->2)-O-beta-D-galactopyranosyl-(1-->2)-beta-D-glucopyranosiduronic acid 101944852 Click to see CC1C(C(C(C(O1)OC2C(C(C(OC2OC3C(C(C(OC3OC4CCC5(C(C4(C)CO)CCC6(C5CC=C7C6(CCC8(C7CC(CC8)(C)C)C(=O)OC9C(C(C(C(O9)CO)O)O)OC1C(C(C(C(O1)C)O)O)O)C)C)C)C(=O)O)O)O)CO)O)O)O)O)O 1265.40 unknown via CMAUP database
(3I(2))-28-(I(2)-D-Glucopyranosyloxy)-28-oxoolean-12-en-3-yl O-6-deoxy-I+/--L-mannopyranosyl-(1a2)-O-I(2)-D-galactopyranosyl-(1a2)-I(2)-D-glucopyranosiduronic acid 101944851 Click to see CC1C(C(C(C(O1)OC2C(C(C(OC2OC3C(C(C(OC3OC4CCC5(C(C4(C)C)CCC6(C5CC=C7C6(CCC8(C7CC(CC8)(C)C)C(=O)OC9C(C(C(C(O9)CO)O)O)O)C)C)C)C(=O)O)O)O)CO)O)O)O)O)O 1103.20 unknown via CMAUP database
Calenduloside F 13909684 Click to see CC1(CCC2(CCC3(C(=CCC4C3(CCC5C4(CCC(C5(C)C)OC6C(C(C(C(O6)C(=O)O)O)O)O)C)C)C2C1)C)C(=O)OC7C(C(C(C(O7)CO)O)O)O)C 795.00 unknown via CMAUP database
Lablaboside B 21591281 Click to see CC1C(C(C(C(O1)OC2C(C(C(OC2OC3C(C(C(OC3OC4CCC5(C(C4(C)CO)CCC6(C5CC=C7C6(CCC8(C7CC(CC8)(C)C)C(=O)OC9C(C(C(C(O9)CO)O)O)O)C)C)C)C(=O)O)O)O)CO)O)O)O)O)O 1119.20 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Tetraterpenoids / Carotenoids / Carotenes
alpha-Carotene 6419725 Click to see CC1=C(C(CCC1)(C)C)C=CC(=CC=CC(=CC=CC=C(C)C=CC=C(C)C=CC2C(=CCCC2(C)C)C)C)C 536.90 unknown via CMAUP database
> 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
(2R,3S,5S,8S,9S,10R,13S,14S,17R)-17-[(2S,3R,4R)-3,4-Dihydroxy-6-methyl-5-methylideneheptan-2-yl]-2,3-dihydroxy-10,13-dimethyl-1,2,3,4,5,7,8,9,11,12,14,15,16,17-tetradecahydrocyclopenta[a]phenanthren-6-one 10983436 Click to see CC(C)C(=C)C(C(C(C)C1CCC2C1(CCC3C2CC(=O)C4C3(CC(C(C4)O)O)C)C)O)O 462.70 unknown via CMAUP database
Castasterone 133534 Click to see CC(C)C(C)C(C(C(C)C1CCC2C1(CCC3C2CC(=O)C4C3(CC(C(C4)O)O)C)C)O)O 464.70 unknown via CMAUP database
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Steroid lactones / Brassinolides and derivatives
28-Homodolicholide 13517132 Click to see CC=C(C(C)C)C(C(C(C)C1CCC2C1(CCC3C2COC(=O)C4C3(CC(C(C4)O)O)C)C)O)O 492.70 unknown via CMAUP database
Brassinolide 115196 Click to see CC(C)C(C)C(C(C(C)C1CCC2C1(CCC3C2COC(=O)C4C3(CC(C(C4)O)O)C)C)O)O 480.70 unknown via CMAUP database
Dolicholide 11038144 Click to see CC(C)C(=C)C(C(C(C)C1CCC2C1(CCC3C2COC(=O)C4C3(CC(C(C4)O)O)C)C)O)O 478.70 unknown via CMAUP database
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Stigmastanes and derivatives
(2R,3S,5S,8S,9S,10R,13S,14S,17R)-17-[(E,2S,3R,4R)-3,4-dihydroxy-5-propan-2-ylhept-5-en-2-yl]-2,3-dihydroxy-10,13-dimethyl-1,2,3,4,5,7,8,9,11,12,14,15,16,17-tetradecahydrocyclopenta[a]phenanthren-6-one 14607933 Click to see CC=C(C(C)C)C(C(C(C)C1CCC2C1(CCC3C2CC(=O)C4C3(CC(C(C4)O)O)C)C)O)O 476.70 unknown via CMAUP database
Stigmasterol 5280794 Click to see CCC(C=CC(C)C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)O)C)C)C(C)C 412.70 unknown via CMAUP database
> Organic acids and derivatives / Carboxylic acids and derivatives / Amino acids, peptides, and analogues / Alpha amino acids and derivatives / Alpha amino acids / D-alpha-amino acids
(2R)-piperidin-1-ium-2-carboxylate 6931662 Click to see C1CC[NH2+]C(C1)C(=O)[O-] 129.16 unknown via CMAUP database
> Organoheterocyclic compounds / Imidazopyrimidines / Purines and purine derivatives / 6-aminopurines / 6-alkylaminopurines
trans-Zeatin 449093 Click to see CC(=CCNC1=NC=NC2=C1NC=N2)CO 219.24 unknown via CMAUP database

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