Pinus palustris - Unknown
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Details Top

Internal ID UUID6440022a08d10481114234
Scientific name Pinus palustris
Authority Mill.
First published in Gard. Dict. ed. 8 : n.º 14 (1768)

Description Top

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Synonyms Top

Scientific name Authority First published in
Pinus longifolia Salisb. Prodr. Stirp. Chap. Allerton : 398 (1796)
Pinus palustris subsp. neogigantea Silba J. Int. Conifer Preserv. Soc. 11: 17 (2004)
Pinus palmieri Manetti ex Gordon Pinetum , Suppl.: 63 (1862)
Pinus australis F.Michx. Hist. Arbr. Forest. 1: 64 (1810)
Pinus taeda var. palustris (Mill.) Castigl. Viagg. Stati Uniti 2: 313 (1790)
Pinus palustris var. excelsa Booth ex J.Forbes Pinet. Woburn. 62. 1839
Pinus australis var. excelsa (Booth ex J.Forbes) Carrière Traité Gén. Conif. 346 1855
Pinus australis var. filius Michx.

Common names Top

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Language Common/alternative name
English florida pine
English georgia pine
English longleaf pine
Spanish pino de hoja larga
Bulgarian Блатен бор
Catalan pi melis
Czech borovice bahenní
German harz-kiefer
German sumpfkiefer
German sumpf-kiefer
Esperanto longfolia pino
Estonian pikaokkaline mänd
Persian کاج درازبرگ
Finnish pitkäneulasmänty
French pin des marais
Hebrew אורן הביצות
Upper Sorbian bahnowa chójna
Icelandic fenjafura
Japanese ダイオウショウ
Japanese ダイオウマツ
Korean 대왕소나무
Lithuanian pelkinė pušis
Norwegian Bokmål sumpfuru
Dutch moerasden
Polish sosna długoigielna
Russian Сосна болотная
udm Кузь лысо пужым
Chinese 長葉松
Chinese 大王松
Chinese 长叶松

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
  • Northern America
    • South-central U.S.A.
      • Texas
    • Southeastern U.S.A.
      • Alabama
      • Arkansas
      • Florida
      • Georgia
      • Louisiana
      • Maryland
      • Mississippi
      • North Carolina
      • South Carolina
      • Virginia

Links to other databases Top

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Database ID/link to page
World Flora Online wfo-0000481804
UNII 724SER9IMN
Florida Plant Atlas 3905
Flora of Alabama 213
USDA Plants PIPA2
Tropicos 24900204
INPN 458778
KEW urn:lsid:ipni.org:names:263186-1
The Plant List kew-2562456
Open Tree Of Life 351667
NCBI Taxonomy 46836
Nature Serve 2.152746
IUCN Red List 39068
IPNI 263186-1
iNaturalist 81901
GBIF 5285816
Freebase /m/02cbmv
FEIS plants/tree/pinpal
EPPO PIUPA
EOL 323452
USDA GRIN 28518
Wikipedia Longleaf_pine
CMAUP NPO20778

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
The genus Fomitopsis (Polyporales, Basidiomycota) reconsidered Spirin V, Runnel K, Vlasák J, Viner I, Barrett MD, Ryvarden L, Bernicchia A, Rivoire B, Ainsworth AM, Grebenc T, Cartabia M, Niemelä T, Larsson KH, Miettinen O Stud Mycol 22-Feb-2024
PMCID:PMC11003443
doi:10.3114/sim.2024.107.03
PMID:38600960
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
Supplement Type Impact on the Performance and Nutrient Dynamics of Nursing Does and Kids Raised in Woodlands Shrestha B, Karki U, Chaudhary S, Tiwari A, Karki LB Animals (Basel) 23-Dec-2023
PMCID:PMC10778155
doi:10.3390/ani14010068
PMID:38200799
Data science competition for cross-site individual tree species identification from airborne remote sensing data Graves SJ, Marconi S, Stewart D, Harmon I, Weinstein B, Kanazawa Y, Scholl VM, Joseph MB, McGlinchy J, Browne L, Sullivan MK, Estrada-Villegas S, Wang DZ, Singh A, Bohlman S, Zare A, White EP PeerJ 21-Dec-2023
PMCID:PMC10749090
doi:10.7717/peerj.16578
PMID:38144190
Transfluthrin diffusers do not protect two-person US military tents from mosquitoes in open field and canopy warm-temperate habitats Bayer BE, Aldridge RL, Moreno BJ, Golden FV, Gibson S, Wahl JL, Linthicum KJ Curr Res Parasitol Vector Borne Dis 30-Nov-2023
PMCID:PMC10770594
doi:10.1016/j.crpvbd.2023.100156
PMID:38187816
Assessing springtime vertebrate prey of sympatric mesopredators in the southeastern United States using metabarcoding analysis Youngmann JL, Lance SL, Kilgo JC, Ruth C, Cantrell J, D’Angelo GJ PLoS One 25-Oct-2023
PMCID:PMC10599563
doi:10.1371/journal.pone.0293270
PMID:37878654
Hurricane wind regimes for forests of North America Cannon JB, Peterson CJ, Godfrey CM, Whelan AW Proc Natl Acad Sci U S A 10-Oct-2023
PMCID:PMC10589672
doi:10.1073/pnas.2309076120
PMID:37816051
Benzophenones-natural metabolites with great Hopes in drug discovery: structures, occurrence, bioactivities, and biosynthesis Ibrahim SR, Fahad ALsiyud D, Alfaeq AY, Mohamed SG, Mohamed GA RSC Adv 04-Aug-2023
PMCID:PMC10402873
doi:10.1039/d3ra02788k
PMID:37546221
Pest categorisation of Hoplolaimus galeatus 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, Migheli Q, Vloutoglou I, Maiorano A, Pautasso M, Reignault PL EFSA J 20-Jul-2023
PMCID:PMC10357347
doi:10.2903/j.efsa.2023.8117
PMID:37485256
Follow‐up of the re‐evaluation of glycerol esters of wood rosins (E 445) as a food additive Younes M, Aquilina G, Degen G, Engel K, Fowler P, Frutos Fernandez MJ, Fürst P, Gürtler R, Husøy T, Manco M, Mennes W, Passamonti S, Moldeus P, Shah R, Waalkens‐Berendsen I, Wright M, Cheyns K, Fitzgerald R, Mirat M, Mortensen A, Ulbrich B, Woutersen R, Laganaro M, Rincon AM, Ruggeri L, Smeraldi C, Gundert‐Remy U EFSA J 19-Jul-2023
PMCID:PMC10355140
doi:10.2903/j.efsa.2023.8110
PMID:37476082
Spatial ecology of translocated raccoons Hill JE, Helton JL, Chipman RB, Gilbert AT, Beasley JC, Dharmarajan G, Rhodes OE Sci Rep 27-Jun-2023
PMCID:PMC10300129
doi:10.1038/s41598-023-37323-6
PMID:37369730
The increasing threat to European forests from the invasive foliar pine pathogen, Lecanosticta acicola Tubby K, Adamčikova K, Adamson K, Akiba M, Barnes I, Boroń P, Bragança H, Bulgakov T, Burgdorf N, Capretti P, Cech T, Cleary M, Davydenko K, Drenkhan R, Elvira-Recuenco M, Enderle R, Gardner J, Georgieva M, Ghelardini L, Husson C, Iturritxa E, Markovskaja S, Mesanza N, Ogris N, Oskay F, Piškur B, Queloz V, Raitelaitytė K, Raposo R, Soukainen M, Strasser L, Vahalík P, Vester M, Mullett M For Ecol Manage 15-May-2023
PMCID:PMC10165473
doi:10.1016/j.foreco.2023.120847
PMID:37193248
Investigation of the Chemical Content and User Comments on Facial Cleansing Products Güder S Sr, Güder H Cureus 07-May-2023
PMCID:PMC10243403
doi:10.7759/cureus.38673
PMID:37288177
Automatic resin duct detection and measurement from wood core images using convolutional neural networks Fabijańska A, Cahalan GD Sci Rep 02-May-2023
PMCID:PMC10154293
doi:10.1038/s41598-023-34304-7
PMID:37130881
Multiple intrinsic and extrinsic drivers influence the quantity and quality components of seed dispersal effectiveness in the rare shrub Lindera subcoriacea Hohmann MG, Wall WA, Just MG, Huskins SD PLoS One 31-Mar-2023
PMCID:PMC10065295
doi:10.1371/journal.pone.0283810
PMID:37000816

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
> Lipids and lipid-like molecules / Prenol lipids / Diterpenoids
1,4a-Dimethyl-7-propan-2-yl-2,3,4,4b,5,6,10,10a-octahydrophenanthrene-1-carboxylic acid 90895 Click to see CC(C)C1=CC2=CCC3C(C2CC1)(CCCC3(C)C(=O)O)C 302.50 unknown https://doi.org/10.1002/ARDP.19022400803
1,4a-Dimethyl-7-propan-2-yl-2,3,4,9,10,10a-hexahydrophenanthrene-1-carboxylic acid 15618 Click to see CC(C)C1=CC2=C(C=C1)C3(CCCC(C3CC2)(C)C(=O)O)C 300.40 unknown https://doi.org/10.1021/JA01191A039
Abieta-8(14),13(15)-dien-18-oic acid 10117 Click to see CC(=C1CCC2C(=C1)CCC3C2(CCCC3(C)C(=O)O)C)C 302.50 unknown https://doi.org/10.1021/JA01191A039
Abietic acid 10569 Click to see CC(C)C1=CC2=CCC3C(C2CC1)(CCCC3(C)C(=O)O)C 302.50 unknown https://doi.org/10.1002/ARDP.19022400803
Dehydroabietic acid 94391 Click to see CC(C)C1=CC2=C(C=C1)C3(CCCC(C3CC2)(C)C(=O)O)C 300.40 unknown https://doi.org/10.1021/JA01191A039
delta8(14)-Pimaric acid 10116 Click to see CC1(CCC2C(=C1)CCC3C2(CCCC3(C)C(=O)O)C)C=C 302.50 unknown https://doi.org/10.1021/JA01336A033
https://doi.org/10.1021/JA01191A039
Dextropimarinal 12304198 Click to see CC1(CCC2C(=C1)CCC3C2(CCCC3(C)C=O)C)C=C 286.50 unknown https://doi.org/10.1021/JA01191A039
Levopimaric acid 221062 Click to see CC(C)C1=CCC2C(=C1)CCC3C2(CCCC3(C)C(=O)O)C 302.50 unknown https://doi.org/10.1021/JA01191A039
https://doi.org/10.1021/JA01336A033
Neoabietic acid 221118 Click to see CC(=C1CCC2C(=C1)CCC3C2(CCCC3(C)C(=O)O)C)C 302.50 unknown https://doi.org/10.1021/JA01191A039
Pimaric acid 220338 Click to see CC1(CCC2C(=C1)CCC3C2(CCCC3(C)C(=O)O)C)C=C 302.50 unknown https://doi.org/10.1021/JA01191A039
https://doi.org/10.1021/JA01336A033
Podocarpa-8(14),12-dien-15-oic acid, 13-isopropyl- 221064 Click to see CC(C)C1=CCC2C(=C1)CCC3C2(CCCC3(C)C(=O)O)C 302.50 unknown https://doi.org/10.1021/JA01191A039
https://doi.org/10.1021/JA01336A033
Retene 10222 Click to see CC1=C2C=CC3=C(C2=CC=C1)C=CC(=C3)C(C)C 234.30 unknown https://doi.org/10.1002/ARDP.19022400803
Sandaracopimarinal 620819 Click to see CC1(CCC2C(=C1)CCC3C2(CCCC3(C)C=O)C)C=C 286.50 unknown https://doi.org/10.1021/JA01191A039
> Lipids and lipid-like molecules / Prenol lipids / Monoterpenoids / Bicyclic monoterpenoids
(-)-3-Carene 442461 Click to see CC1=CCC2C(C1)C2(C)C 136.23 unknown https://doi.org/10.1016/S0031-9422(00)89063-9
(-)-beta-Pinene 440967 Click to see CC1(C2CCC(=C)C1C2)C 136.23 unknown https://doi.org/10.1039/JR9290000305
(+)-alpha-Pinene 82227 Click to see CC1=CCC2CC1C2(C)C 136.23 unknown https://doi.org/10.1039/JR9290000305
3-Carene 26049 Click to see CC1=CCC2C(C1)C2(C)C 136.23 unknown https://doi.org/10.1016/S0031-9422(00)89063-9
alpha-PINENE 6654 Click to see CC1=CCC2CC1C2(C)C 136.23 unknown https://doi.org/10.1039/JR9290000305
beta-Pinene 14896 Click to see CC1(C2CCC(=C)C1C2)C 136.23 unknown https://doi.org/10.1039/JR9290000305
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids
(+)-Longifolene 1796220 Click to see CC1(CCCC2(C3C1C(C2=C)CC3)C)C 204.35 unknown https://doi.org/10.1002/CBER.19620950804
Longifolene 289151 Click to see CC1(CCCC2(C3C1C(C2=C)CC3)C)C 204.35 unknown https://doi.org/10.1002/CBER.19620950804
> Lipids and lipid-like molecules / Prenol lipids / Triterpenoids
(Z,6S)-2-methyl-6-[(5R,9S,10R,13S,14S,17S)-4,4,10,13,14-pentamethyl-3-oxo-1,2,5,6,9,11,12,15,16,17-decahydrocyclopenta[a]phenanthren-17-yl]hept-2-enoic acid 51693592 Click to see CC(CCC=C(C)C(=O)O)C1CCC2(C1(CCC3C2=CCC4C3(CCC(=O)C4(C)C)C)C)C 454.70 unknown via CMAUP database
3-Epioleanolic acid 11869658 Click to see CC1(CCC2(CCC3(C(=CCC4C3(CCC5C4(CCC(C5(C)C)O)C)C)C2C1)C)C(=O)O)C 456.70 unknown via CMAUP database
3beta-Hydroxyfriedelan-16-one 101679786 Click to see CC1C(CCC2C1(CCC3C2(CCC4(C3(CC(=O)C5(C4CC(CC5)(C)C)C)C)C)C)C)O 442.70 unknown via CMAUP database
Friedelin 91472 Click to see CC1C(=O)CCC2C1(CCC3C2(CCC4(C3(CCC5(C4CC(CC5)(C)C)C)C)C)C)C 426.70 unknown via CMAUP database
Maytensifolin B 21636453 Click to see CC1C(=O)CCC2C1(CCC3C2(CCC4(C3(CC(=O)C5(C4CC(CC5)(C)C)C)C)C)C)C 440.70 unknown via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Biflavonoids and polyflavonoids
Amentoflavone 5281600 Click to see C1=CC(=CC=C1C2=CC(=O)C3=C(O2)C(=C(C=C3O)O)C4=C(C=CC(=C4)C5=CC(=O)C6=C(C=C(C=C6O5)O)O)O)O 538.50 unknown via CMAUP database
Podocarpusflavone A 5320644 Click to see COC1=CC=C(C=C1)C2=CC(=O)C3=C(O2)C(=C(C=C3O)O)C4=C(C=CC(=C4)C5=CC(=O)C6=C(C=C(C=C6O5)O)O)O 552.50 unknown via CMAUP database
Putraflavone 5320646 Click to see COC1=CC=C(C=C1)C2=CC(=O)C3=C(O2)C(=C(C=C3O)O)C4=C(C=CC(=C4)C5=CC(=O)C6=C(C=C(C=C6O5)OC)O)O 566.50 unknown via CMAUP database
> Phenylpropanoids and polyketides / Stilbenes
Pinosylvin methyl ether 5281719 Click to see COC1=CC(=CC(=C1)O)C=CC2=CC=CC=C2 226.27 unknown https://doi.org/10.1016/0031-9422(93)85098-C

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