Manoao colensoi - Unknown
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Internal ID UUID643ffe574eacb617429171
Scientific name Manoao colensoi
Authority (Hook.) Molloy
First published in New Zealand J. Bot. 33: 196 (1995)

Description Top

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Manoao is a unique genus in the Podocarpaceae family, consisting of only one species, M. colensoi. This species, also known as manoao, silver pine, Westland pine, or white silver pine, is native to New Zealand. It was previously classified in the Dacrydium or Lagarostrobos genus, but has since been recognized as its own distinct genus. Some botanists still consider it part of Lagarostrobos due to its close relation. Manoao is closely related to Parasitaxus, a parasitic genus from New Caledonia, and Lagarostrobos, a single species from Tasmania. Manoao colensoi is a slow-growing evergreen tree that can reach up to 15 meters in height. It is typically found in shady, wet areas of New Zealand and is known for its fine, straight, and durable timber. This species is mainly found in the central North Island and western South Island of New Zealand.

Synonyms Top

Scientific name Authority First published in
Lagarostrobos colensoi (Hook.) Quinn Austral. J. Bot. 30: 317 (1982)
Dacrydium colensoi Hook. Hooker's Icon. Pl. 6: t. 548 (1843)
Dacrydium westlandicum Kirk Hooker's Icon. Pl. 13: t. 1218 (1877)
Lepidothamnus colensoi (Hook.) de Laub. Novon 24: 131 (2015)

Common names Top

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Language Common/alternative name
English silver pine
Japanese マノアオ
Norwegian Bokmål manao
Norwegian Bokmål manaoslekten
Chinese 銀松

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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

Links to other databases Top

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Database ID/link to page
World Flora Online wfo-0000452570
Tropicos 50057391
KEW urn:lsid:ipni.org:names:988952-1
The Plant List kew-2509331
Open Tree Of Life 309869
NCBI Taxonomy 120598
IUCN Red List 42482
IPNI 988952-1
iNaturalist 135858
GBIF 2687870
Freebase /m/03wmrf
EOL 1033613
USDA GRIN 463491
Wikipedia Manoao

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
Projecting Podocarpaceae response to climate change: we are not out of the woods yet Twala TC, Fisher JT, Glennon KL AoB Plants 08-Jun-2023
PMCID:PMC10321399
doi:10.1093/aobpla/plad034
PMID:37415722
Diversity, Distribution, Systematics and Conservation Status of Podocarpaceae Khan R, Hill RS, Liu J, Biffin E Plants (Basel) 03-Mar-2023
PMCID:PMC10005643
doi:10.3390/plants12051171
PMID:36904033
Detailed seed cone morpho-anatomy of the Prumnopityoid clade: an insight into the origin and evolution of Podocarpaceae seed cones Khan R, Hill RS, Dörken VM, Biffin E Ann Bot 30-Jul-2022
PMCID:PMC9670759
doi:10.1093/aob/mcac097
PMID:35906916
Loss of the IR region in conifer plastomes: Changes in the selection pressure and substitution rate of protein‐coding genes Ping J, Hao J, Li J, Yang Y, Su Y, Wang T Ecol Evol 12-Jan-2022
PMCID:PMC8809450
doi:10.1002/ece3.8499
PMID:35136556
The thionin family of antimicrobial peptides Höng K, Austerlitz T, Bohlmann T, Bohlmann H PLoS One 14-Jul-2021
PMCID:PMC8279376
doi:10.1371/journal.pone.0254549
PMID:34260649
Plastome Reduction in the Only Parasitic Gymnosperm Parasitaxus Is Due to Losses of Photosynthesis but Not Housekeeping Genes and Apparently Involves the Secondary Gain of a Large Inverted Repeat Qu XJ, Fan SJ, Wicke S, Yi TS Genome Biol Evol 27-Aug-2019
PMCID:PMC6786476
doi:10.1093/gbe/evz187
PMID:31504501
Evolutionary Analysis of MIKCc-Type MADS-Box Genes in Gymnosperms and Angiosperms Chen F, Zhang X, Liu X, Zhang L Front Plant Sci 30-May-2017
PMCID:PMC5447709
doi:10.3389/fpls.2017.00895
PMID:28611810
First record of Podocarpoid fossil wood in South China Li L, Jin JH, Quan C, Oskolski AA Sci Rep 30-Aug-2016
PMCID:PMC5004120
doi:10.1038/srep32294
PMID:27571780
DNA Barcode Identification of Podocarpaceae—The Second Largest Conifer Family Little DP, Knopf P, Schulz C PLoS One 27-Nov-2013
PMCID:PMC3842326
doi:10.1371/journal.pone.0081008
PMID:24312258
Disturbance regimes, gap‐demanding trees and seed mass related to tree height in warm temperate rain forests worldwide Grubb PJ, Bellingham PJ, Kohyama TS, Piper FI, Valido A Biol Rev Camb Philos Soc 19-Mar-2013
PMCID:PMC7161821
doi:10.1111/brv.12029
PMID:23506298
Rapid landscape transformation in South Island, New Zealand, following initial Polynesian settlement McWethy DB, Whitlock C, Wilmshurst JM, McGlone MS, Fromont M, Li X, Dieffenbacher-Krall A, Hobbs WO, Fritz SC, Cook ER Proc Natl Acad Sci U S A 07-Dec-2010
PMCID:PMC3003061
doi:10.1073/pnas.1011801107
PMID:21149690
Paradise burnt: How colonizing humans transform landscapes with fire Bowman DM, Haberle SG Proc Natl Acad Sci U S A 30-Nov-2010
PMCID:PMC3003002
doi:10.1073/pnas.1016393108
PMID:21149739
The diterpenes of Dacrydium colensoi. VIII. Sandaracopimaradien-19-ol and 2α-Carboxycolensen-2β-ol PK Grant, C Huntrakul, JM Robertson CSIRO Publishing 02-Sep-2010
doi:10.1071/CH9691265
Essential oils of New Zealand podocarpaceae. I. <i>Dacrydium colensoi</i> J. D. Briasco, J. Murray Wiley 05-Jul-2010
doi:10.1002/JCTB.5010020405
Über die Diterpenoxyde des Harzes von Dacrydium Colensoi (I. Mitteil.) J. R. Hosking, C. W. Brandt Wiley 20-Jul-2007
doi:10.1002/CBER.19340670710

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
> Alkaloids and derivatives / Erythrina alkaloids / Homoerythrinane alkaloids
(1S,17S)-4,5,17-trimethoxy-11-azatetracyclo[9.7.0.0^{1,14.0^{2,7]octadeca-2,4,6,14-tetraene 3979007 Click to see COC1CC=C2CCN3C2(C1)C4=CC(=C(C=C4CCC3)OC)OC 329.40 unknown https://doi.org/10.1016/0031-9422(95)00030-5
(1S,17S)-4,5,6,17-tetramethoxy-11-azatetracyclo[9.7.0.01,14.02,7]octadeca-2,4,6,14-tetraene 101690776 Click to see COC1CC=C2CCN3C2(C1)C4=CC(=C(C(=C4CCC3)OC)OC)OC 359.50 unknown https://doi.org/10.1016/0031-9422(95)00030-5
(1S,17S)-5,6,17-trimethoxy-11-azatetracyclo[9.7.0.01,14.02,7]octadeca-2,4,6,14-tetraen-4-ol 101691087 Click to see COC1CC=C2CCN3C2(C1)C4=CC(=C(C(=C4CCC3)OC)OC)O 345.40 unknown https://doi.org/10.1016/0031-9422(95)00030-5
(1S,19S)-19-methoxy-13-azapentacyclo[11.7.0.01,16.02,9.04,7]icosa-2,4(7),8,16-tetraene 163071783 Click to see COC1CC=C2CCN3C2(C1)C4=CC5=C(CC5)C=C4CCC3 295.40 unknown https://doi.org/10.1016/0031-9422(95)00030-5
(1S,19S)-8,19-dimethoxy-13-azapentacyclo[11.7.0.01,16.02,9.04,7]icosa-2(9),3,7,16-tetraene 162965721 Click to see COC1CC=C2CCN3C2(C1)C4=C(CCC3)C(=C5CCC5=C4)OC 325.40 unknown https://doi.org/10.1016/0031-9422(95)00030-5
(1S,20S)-9,20-dimethoxy-5,7-dioxa-14-azapentacyclo[12.7.0.01,17.02,10.04,8]henicosa-2,4(8),9,17-tetraene 14061845 Click to see COC1CC=C2CCN3C2(C1)C4=CC5=C(C(=C4CCC3)OC)OCO5 343.40 unknown https://doi.org/10.1016/0031-9422(95)00030-5
19-Methoxy-13-azapentacyclo[11.7.0.01,16.02,9.04,7]icosa-2,4(7),8,16-tetraene 163071782 Click to see COC1CC=C2CCN3C2(C1)C4=CC5=C(CC5)C=C4CCC3 295.40 unknown https://doi.org/10.1016/0031-9422(95)00030-5
2,7-Dihydrohomoerysotrine 296195 Click to see COC1CC=C2CCN3C2(C1)C4=CC(=C(C=C4CCC3)OC)OC 329.40 unknown https://doi.org/10.1016/0031-9422(95)00030-5
4,5,6,17-Tetramethoxy-11-azatetracyclo[9.7.0.01,14.02,7]octadeca-2,4,6,14-tetraene 14286108 Click to see COC1CC=C2CCN3C2(C1)C4=CC(=C(C(=C4CCC3)OC)OC)OC 359.50 unknown https://doi.org/10.1016/0031-9422(95)00030-5
5,6,17-Trimethoxy-11-azatetracyclo[9.7.0.01,14.02,7]octadeca-2,4,6,14-tetraen-4-ol 14286110 Click to see COC1CC=C2CCN3C2(C1)C4=CC(=C(C(=C4CCC3)OC)OC)O 345.40 unknown https://doi.org/10.1016/0031-9422(95)00030-5
8,19-Dimethoxy-13-azapentacyclo[11.7.0.01,16.02,9.04,7]icosa-2(9),3,7,16-tetraene 162965720 Click to see COC1CC=C2CCN3C2(C1)C4=C(CCC3)C(=C5CCC5=C4)OC 325.40 unknown https://doi.org/10.1016/0031-9422(95)00030-5
> Lipids and lipid-like molecules / Prenol lipids / Diterpenoids
7-Ethenyl-1,1,4a,7-tetramethyl-2,3,4,4b,5,6,8,9,10,10a-decahydrophenanthren-8a-ol 13969543 Click to see CC1(CCCC2(C1CCC3(C2CCC(C3)(C)C=C)O)C)C 290.50 unknown https://doi.org/10.1039/J39670000300
Nezukol 13969544 Click to see CC1(CCCC2(C1CCC3(C2CCC(C3)(C)C=C)O)C)C 290.50 unknown https://doi.org/10.1039/J39670000300
Podocarp-8(14)-ene, 13beta-methyl-13-vinyl- 519326 Click to see CC1(CCCC2(C1CCC3=CC(CCC32)(C)C=C)C)C 272.50 unknown https://doi.org/10.1039/J39670000300
Sandaracopimaradiene 443469 Click to see CC1(CCCC2(C1CCC3=CC(CCC32)(C)C=C)C)C 272.50 unknown https://doi.org/10.1039/J39670000300
> Lipids and lipid-like molecules / Prenol lipids / Diterpenoids / Kaurane diterpenoids
(-)-Isokaurene 521318 Click to see CC1=CC23CCC4C(CCCC4(C2CCC1C3)C)(C)C 272.50 unknown https://doi.org/10.1039/J39670000300
(1R,4S,9S,10R,13S)-5,5,9,14-tetramethyltetracyclo[11.2.1.01,10.04,9]hexadec-14-ene 12311057 Click to see CC1=CC23CCC4C(CCCC4(C2CCC1C3)C)(C)C 272.50 unknown https://doi.org/10.1039/J39670000300
(1S,4S,9S,10S,13R)-5,5,9-trimethyl-14-methylidenetetracyclo[11.2.1.01,10.04,9]hexadecane 101289537 Click to see CC1(CCCC2(C1CCC34C2CCC(C3)C(=C)C4)C)C 272.50 unknown https://doi.org/10.1039/J39670000300
Kaur-16-ene 520687 Click to see CC1(CCCC2(C1CCC34C2CCC(C3)C(=C)C4)C)C 272.50 unknown https://doi.org/10.1039/J39670000300
> Lipids and lipid-like molecules / Prenol lipids / Monoterpenoids / Acyclic monoterpenoids
Myrcene 31253 Click to see CC(=CCCC(=C)C=C)C 136.23 unknown https://doi.org/10.1002/JCTB.5010020405
> 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/JCTB.5010020405
Longifolene 289151 Click to see CC1(CCCC2(C3C1C(C2=C)CC3)C)C 204.35 unknown https://doi.org/10.1002/JCTB.5010020405
> Lipids and lipid-like molecules / Prenol lipids / Triterpenoids
(3R,4aR,6aR,8S,9aS,9bR)-3-ethenyl-8-hydroxy-3,4a,7,7,9a-pentamethyl-2,5,6,6a,9,9b-hexahydro-1H-cyclopenta[f]chromene-8-carboxylic acid 101600189 Click to see CC1(C2CCC3(C(C2(CC1(C(=O)O)O)C)CCC(O3)(C)C=C)C)C 336.50 unknown https://doi.org/10.1071/CH9691265
(3R,4aR,6aS,7S,10aS,10bR)-3-ethenyl-7-(hydroxymethyl)-3,4a,7,10a-tetramethyl-1,2,5,6,6a,8,10,10b-octahydrobenzo[f]chromen-9-one 163105821 Click to see CC1(CCC2C(O1)(CCC3C2(CC(=O)CC3(C)CO)C)C)C=C 320.50 unknown https://doi.org/10.1016/S0040-4020(01)96976-5
(3R,4aR,6aS,9S,10aS,10bR)-3-ethenyl-3,4a,7,7,10a-pentamethyl-2,5,6,6a,8,9,10,10b-octahydro-1H-benzo[f]chromen-9-ol 21593578 Click to see CC1(CC(CC2(C1CCC3(C2CCC(O3)(C)C=C)C)C)O)C 306.50 unknown https://doi.org/10.1039/JR9650003846
3-ethenyl-3,4a,7,7,10a-pentamethyl-2,5,6,6a,8,9,10,10b-octahydro-1H-benzo[f]chromene 518574 Click to see CC1(CCCC2(C1CCC3(C2CCC(O3)(C)C=C)C)C)C 290.50 unknown https://doi.org/10.1002/CBER.19340670710
CID 13966380 13966380 Click to see CC1(CC(=O)CC2(C1CCC3(C2CCC(O3)(C)C=C)C)C)C 304.50 unknown https://doi.org/10.1002/CBER.19340670710
https://doi.org/10.1071/CH9900791
Labd-14-en-2-one, 8,13-epoxy-, (13R)- 625784 Click to see CC1(CC(=O)CC2(C1CCC3(C2CCC(O3)(C)C=C)C)C)C 304.50 unknown https://doi.org/10.1002/CBER.19340670710
Labd-14-ene, 8,13-epoxy-, (13S)- 6432025 Click to see CC1(CCCC2(C1CCC3(C2CCC(O3)(C)C=C)C)C)C 290.50 unknown https://doi.org/10.1002/CBER.19340670710
https://doi.org/10.1071/CH9900791
> Organoheterocyclic compounds / Azaspirodecane derivatives
methyl (1R,3S,11R,13R,14E)-3-methoxy-14-(2-methoxy-2-oxoethylidene)-9-azatetracyclo[7.5.0.01,6.011,13]tetradec-5-ene-13-carboxylate 101691088 Click to see COC1CC=C2CCN3C2(C1)C(=CC(=O)OC)C4(CC4C3)C(=O)OC 347.40 unknown https://doi.org/10.1016/0031-9422(95)00030-5
methyl (1S,3S,11R,13R,14E)-3-methoxy-14-(2-methoxy-2-oxoethylidene)-9-azatetracyclo[7.5.0.01,6.011,13]tetradec-5-ene-13-carboxylate 163185593 Click to see COC1CC=C2CCN3C2(C1)C(=CC(=O)OC)C4(CC4C3)C(=O)OC 347.40 unknown https://doi.org/10.1016/0031-9422(95)00030-5
> Organoheterocyclic compounds / Benzopyrans
2-[(2R,4aS,5S,6R,8aR)-5-(carboxymethyl)-2-ethenyl-2,5,8a-trimethyl-3,4,4a,6,7,8-hexahydrochromen-6-yl]-2-methylpropanoic acid 38347088 Click to see CC1(CCC2C(O1)(CCC(C2(C)CC(=O)O)C(C)(C)C(=O)O)C)C=C 352.50 unknown https://doi.org/10.1039/JR9650003846
> Organoheterocyclic compounds / Lactones / Delta valerolactones
(4aS,6aR,8R,10aR,10bS)-8-ethenyl-4,4,6a,8,10b-pentamethyl-4a,5,6,9,10,10a-hexahydro-1H-pyrano[4,3-f]chromen-2-one 162891941 Click to see CC1(C2CCC3(C(C2(CC(=O)O1)C)CCC(O3)(C)C=C)C)C 306.40 unknown https://doi.org/10.1039/JR9650003846
> Organoheterocyclic compounds / Oxanes
(1S,2R,5R,7R,10R,12S,16S)-5-ethenyl-12-hydroxy-1,5,7,11,11-pentamethyl-6,14-dioxatetracyclo[8.6.0.02,7.012,16]hexadecan-13-one 163185076 Click to see CC1(C2CCC3(C(C2(C4C1(C(=O)OC4)O)C)CCC(O3)(C)C=C)C)C 348.50 unknown https://doi.org/10.1016/S0040-4020(01)93012-1
(1S,2S,5R,7R,10R,12S,16S)-5-ethenyl-12-hydroxy-1,5,7,11,11-pentamethyl-6,14-dioxatetracyclo[8.6.0.02,7.012,16]hexadecan-13-one 162891908 Click to see CC1(C2CCC3(C(C2(C4C1(C(=O)OC4)O)C)CCC(O3)(C)C=C)C)C 348.50 unknown https://doi.org/10.1016/S0040-4020(01)93013-3
5-Ethenyl-12-hydroxy-1,5,7,11,11-pentamethyl-6,14-dioxatetracyclo[8.6.0.02,7.012,16]hexadecan-13-one 162891907 Click to see CC1(C2CCC3(C(C2(C4C1(C(=O)OC4)O)C)CCC(O3)(C)C=C)C)C 348.50 unknown https://doi.org/10.1016/S0040-4020(01)93012-1
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid O-glycosides / Flavonoid-3-O-glycosides
Astragalin 5282102 Click to see C1=CC(=CC=C1C2=C(C(=O)C3=C(C=C(C=C3O2)O)O)OC4C(C(C(C(O4)CO)O)O)O)O 448.40 unknown https://doi.org/10.1021/NP50052A014
Hyperoside 5281643 Click to see C1=CC(=C(C=C1C2=C(C(=O)C3=C(C=C(C=C3O2)O)O)OC4C(C(C(C(O4)CO)O)O)O)O)O 464.40 unknown https://doi.org/10.1021/NP50052A014
Quercitrin 5280459 Click to see CC1C(C(C(C(O1)OC2=C(OC3=CC(=CC(=C3C2=O)O)O)C4=CC(=C(C=C4)O)O)O)O)O 448.40 unknown https://doi.org/10.1021/NP50052A014
Trifolin 5282149 Click to see C1=CC(=CC=C1C2=C(C(=O)C3=C(C=C(C=C3O2)O)O)OC4C(C(C(C(O4)CO)O)O)O)O 448.40 unknown https://doi.org/10.1021/NP50052A014

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