PlantaeDB Logo
Login Sign-up

Dactylanthus taylorii

Dactylanthus taylorii - Unknown
Part: Unknown
Author: Public Domain - WikiMedia
Upload a new image!

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 UUID6440159fe1c4d861510683
Scientific name Dactylanthus taylorii
Authority Hook.f.
First published in Trans. Linn. Soc. London 22: 425 (1859)

Description Top

Suggest a correction or write a new one!
No description added yet. Help us by writing one.

Synonyms Top

No known synonyms.

Common names Top

Add a new one! Suggest a correction!

Language Common/alternative name
English wood rose
English flower of hades
Finnish manankukka
mi waewae atua
mi pua o te rēinga

Subspecies (abbr. subsp./ssp.) Top

Add a new one! Suggest a correction!
No subspecies added yet.

Varieties (abbr. var.) Top

Add a new one! Suggest a correction!
No variety added yet.

Subvarieties (abbr. subvar.) Top

Add a new one! Suggest a correction!
No subvariety added yet.

Forms (abbr. f.) Top

Add a new one! Suggest a correction!
No forms added yet.

Germination/Propagation Top

Suggest a correction or add new data!
No germination or propagation data was added yet.

Distribution (via POWO/KEW) Top

Legend for the distribution data:
- Doubtful data
- Extinct
- Introduced
- Native

Links to other databases Top

Suggest others/fix!
Database ID/link to page
World Flora Online wfo-0000636808
Tropicos 100320382
KEW urn:lsid:ipni.org:names:103338-1
The Plant List kew-2755201
Open Tree Of Life 129742
NCBI Taxonomy 328070
IPNI 103338-1
iNaturalist 337655
GBIF 5687181
Freebase /m/027nvf
EOL 5604518
Wikipedia Dactylanthus_taylorii

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
Parasitic plant, from inside out: endophytic development in Lathrophytum peckoltii (Balanophoraceae) in host liana roots from tribe Paullineae (Sapindaceae) Pellissari LC, Teixeira-Costa L, Ceccantini G, Tamaio N, Cardoso LJ, Braga JM, Barros CF Ann Bot 09-Dec-2021
PMCID:PMC8835641
doi:10.1093/aob/mcab148
PMID:34888616
Embryology in Helosis cayennensis (Balanophoraceae): Structure of Female Flowers, Fruit, Endosperm and Embryo Gonzalez AM, Sato HA, Marazzi B Plants (Basel) 22-Mar-2019
PMCID:PMC6473523
doi:10.3390/plants8030074
PMID:30909493
Center for Plant Conservation's Best Practice Guidelines for the reintroduction of rare plants Maschinski J, Albrecht MA Plant Divers 28-Sep-2017
PMCID:PMC6112315
doi:10.1016/j.pld.2017.09.006
PMID:30159534
Time to Spread Your Wings: A Review of the Avian Ancient DNA Field Grealy A, Rawlence NJ, Bunce M Genes (Basel) 18-Jul-2017
PMCID:PMC5541317
doi:10.3390/genes8070184
PMID:28718817
Miocene Fossils Reveal Ancient Roots for New Zealand’s Endemic Mystacina (Chiroptera) and Its Rainforest Habitat Hand SJ, Lee DE, Worthy TH, Archer M, Worthy JP, Tennyson AJ, Salisbury SW, Scofield RP, Mildenhall DC, Kennedy EM, Lindqvist JK PLoS One 17-Jun-2015
PMCID:PMC4470663
doi:10.1371/journal.pone.0128871
PMID:26083758
Bats that walk: a new evolutionary hypothesis for the terrestrial behaviour of New Zealand's endemic mystacinids Hand SJ, Weisbecker V, Beck RM, Archer M, Godthelp H, Tennyson AJ, Worthy TH BMC Evol Biol 20-Jul-2009
PMCID:PMC2729772
doi:10.1186/1471-2148-9-169
PMID:19615105
Evolution of New Zealand's terrestrial fauna: a review of molecular evidence Goldberg J, Trewick SA, Paterson AM Philos Trans R Soc Lond B Biol Sci 04-Sep-2008
PMCID:PMC2607375
doi:10.1098/rstb.2008.0114
PMID:18782728
Volatile constituents of Dactylanthus taylorii flower nectar in relation to flower pollination and browsing by animals C.E. Ecroyd, R.A. Franich, H.W. Kroese, D. Steward Elsevier BV 13-May-2003
doi:10.1016/0031-9422(95)00403-T

Phytochemical Profile Top

Add a new one!
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 / Benzene and substituted derivatives
Phenylethyl Alcohol 6054 Click to see C1=CC=C(C=C1)CCO 122.16 unknown https://doi.org/10.1016/0031-9422(95)00403-T
> Benzenoids / Benzene and substituted derivatives / Benzoic acids and derivatives / Benzoic acid esters
Ethyl benzoate 7165 Click to see CCOC(=O)C1=CC=CC=C1 150.17 unknown https://doi.org/10.1016/0031-9422(95)00403-T
> Benzenoids / Benzene and substituted derivatives / Benzoic acids and derivatives / Benzoic acid esters / o-Hydroxybenzoic acid esters
Ethyl salicylate 8365 Click to see CCOC(=O)C1=CC=CC=C1O 166.17 unknown https://doi.org/10.1016/0031-9422(95)00403-T
> Benzenoids / Benzene and substituted derivatives / Benzoyl derivatives
4-Methylbenzaldehyde 7725 Click to see CC1=CC=C(C=C1)C=O 120.15 unknown https://doi.org/10.1016/0031-9422(95)00403-T
> Benzenoids / Benzene and substituted derivatives / Benzyl alcohols
Benzyl Alcohol 244 Click to see C1=CC=C(C=C1)CO 108.14 unknown https://doi.org/10.1016/0031-9422(95)00403-T
> Benzenoids / Benzene and substituted derivatives / Benzyloxycarbonyls
Benzyl palmitate 13908925 Click to see CCCCCCCCCCCCCCCC(=O)OCC1=CC=CC=C1 346.50 unknown https://doi.org/10.1016/0031-9422(95)00403-T
> Benzenoids / Benzene and substituted derivatives / Phenylacetaldehydes
Phenylacetaldehyde 998 Click to see C1=CC=C(C=C1)CC=O 120.15 unknown https://doi.org/10.1016/0031-9422(95)00403-T
> Hydrocarbons / Saturated hydrocarbons / Alkanes
Heneicosane 12403 Click to see CCCCCCCCCCCCCCCCCCCCC 296.60 unknown https://doi.org/10.1016/0031-9422(95)00403-T
Hentriacontane 12410 Click to see CCCCCCCCCCCCCCCCCCCCCCCCCCCCCCC 436.80 unknown https://doi.org/10.1016/0031-9422(95)00403-T
Heptacosane 11636 Click to see CCCCCCCCCCCCCCCCCCCCCCCCCCC 380.70 unknown https://doi.org/10.1016/0031-9422(95)00403-T
Hexacosane 12407 Click to see CCCCCCCCCCCCCCCCCCCCCCCCCC 366.70 unknown https://doi.org/10.1016/0031-9422(95)00403-T
Nonacosane 12409 Click to see CCCCCCCCCCCCCCCCCCCCCCCCCCCCC 408.80 unknown https://doi.org/10.1016/0031-9422(95)00403-T
Octacosane 12408 Click to see CCCCCCCCCCCCCCCCCCCCCCCCCCCC 394.80 unknown https://doi.org/10.1016/0031-9422(95)00403-T
Pentacosane 12406 Click to see CCCCCCCCCCCCCCCCCCCCCCCCC 352.70 unknown https://doi.org/10.1016/0031-9422(95)00403-T
Tetracosane 12592 Click to see CCCCCCCCCCCCCCCCCCCCCCCC 338.70 unknown https://doi.org/10.1016/0031-9422(95)00403-T
Tricosane 12534 Click to see CCCCCCCCCCCCCCCCCCCCCCC 324.60 unknown https://doi.org/10.1016/0031-9422(95)00403-T
> Lipids and lipid-like molecules / Fatty Acyls / Fatty acid esters
2-Butenoic acid, ethyl ester 12191 Click to see CCOC(=O)C=CC 114.14 unknown https://doi.org/10.1016/0031-9422(95)00403-T
Ethyl crotonate 429065 Click to see CCOC(=O)C=CC 114.14 unknown https://doi.org/10.1016/0031-9422(95)00403-T
Ethyl palmitate 12366 Click to see CCCCCCCCCCCCCCCC(=O)OCC 284.50 unknown https://doi.org/10.1016/0031-9422(95)00403-T
> Lipids and lipid-like molecules / Fatty Acyls / Fatty acids and conjugates / Long-chain fatty acids
Palmitic Acid 985 Click to see CCCCCCCCCCCCCCCC(=O)O 256.42 unknown https://doi.org/10.1016/0031-9422(95)00403-T
> Lipids and lipid-like molecules / Prenol lipids / Monoterpenoids / Acyclic monoterpenoids
3,7-Dimethyl-2,6-octadien-1-ol 4458 Click to see CC(=CCCC(=CCO)C)C 154.25 unknown https://doi.org/10.1016/0031-9422(95)00403-T
Geraniol 637566 Click to see CC(=CCCC(=CCO)C)C 154.25 unknown https://doi.org/10.1016/0031-9422(95)00403-T
Nerol 643820 Click to see CC(=CCCC(=CCO)C)C 154.25 unknown https://doi.org/10.1016/0031-9422(95)00403-T
> Lipids and lipid-like molecules / Prenol lipids / Triterpenoids
Squalene 638072 Click to see CC(=CCCC(=CCCC(=CCCC=C(C)CCC=C(C)CCC=C(C)C)C)C)C 410.70 unknown https://doi.org/10.1016/0031-9422(95)00403-T
Super Squalene; trans-Squalene;AddaVax 1105 Click to see CC(=CCCC(=CCCC(=CCCC=C(C)CCC=C(C)CCC=C(C)C)C)C)C 410.70 unknown https://doi.org/10.1016/0031-9422(95)00403-T
> Organic acids and derivatives / Hydroxy acids and derivatives / Beta hydroxy acids and derivatives
Ethyl 3-hydroxybutyrate 62572 Click to see CCOC(=O)CC(C)O 132.16 unknown https://doi.org/10.1016/0031-9422(95)00403-T
> Organic oxygen compounds / Organooxygen compounds / Alcohols and polyols / Primary alcohols
2-Methyl-2-buten-1-OL 6433417 Click to see CC=C(C)CO 86.13 unknown https://doi.org/10.1016/0031-9422(95)00403-T
2-Methylbut-2-en-1-ol 20799 Click to see CC=C(C)CO 86.13 unknown https://doi.org/10.1016/0031-9422(95)00403-T
3-Methyl-3-buten-1-ol 12988 Click to see CC(=C)CCO 86.13 unknown https://doi.org/10.1016/0031-9422(95)00403-T
Isoamyl alcohol 31260 Click to see CC(C)CCO 88.15 unknown https://doi.org/10.1016/0031-9422(95)00403-T
> Organic oxygen compounds / Organooxygen compounds / Alcohols and polyols / Secondary alcohols
(S)-(+)-3-Methyl-2-butanol 6999784 Click to see CC(C)C(C)O 88.15 unknown https://doi.org/10.1016/0031-9422(95)00403-T
3-Methyl-2-butanol 11732 Click to see CC(C)C(C)O 88.15 unknown https://doi.org/10.1016/0031-9422(95)00403-T
3-Methyl-3-buten-2-ol 66329 Click to see CC(C(=C)C)O 86.13 unknown https://doi.org/10.1016/0031-9422(95)00403-T
3-Methyl-3-buten-2-ol, (R)- 10678185 Click to see CC(C(=C)C)O 86.13 unknown https://doi.org/10.1016/0031-9422(95)00403-T
> Organic oxygen compounds / Organooxygen compounds / Carbonyl compounds / Aldehydes / Aryl-aldehydes
Furfural 7362 Click to see C1=COC(=C1)C=O 96.08 unknown https://doi.org/10.1016/0031-9422(95)00403-T
> Organic oxygen compounds / Organooxygen compounds / Carbonyl compounds / Alpha,beta-unsaturated aldehydes / Enals
3-Methyl-2-butenal 61020 Click to see CC(=CC=O)C 84.12 unknown https://doi.org/10.1016/0031-9422(95)00403-T
> Organoheterocyclic compounds / Pyrans
(2S)-4-methyl-2-(2-methylprop-1-enyl)-3,6-dihydro-2H-pyran 11062576 Click to see CC1=CCOC(C1)C=C(C)C 152.23 unknown https://doi.org/10.1016/0031-9422(95)00403-T
Nerol oxide 61275 Click to see CC1=CCOC(C1)C=C(C)C 152.23 unknown https://doi.org/10.1016/0031-9422(95)00403-T
> Phenylpropanoids and polyketides / Cinnamic acids and derivatives / Cinnamic acid esters
Ethyl 3-phenylprop-2-enoate 7649 Click to see CCOC(=O)C=CC1=CC=CC=C1 176.21 unknown https://doi.org/10.1016/0031-9422(95)00403-T
Ethyl cinnamate 637758 Click to see CCOC(=O)C=CC1=CC=CC=C1 176.21 unknown https://doi.org/10.1016/0031-9422(95)00403-T
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid O-glycosides / Flavonoid-7-O-glycosides
[(2S,3R,4S,5S,6R)-4,5-dihydroxy-6-(hydroxymethyl)-2-[2-(4-hydroxyphenyl)-4-oxo-7-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxychromen-8-yl]oxan-3-yl] (E)-3-(4-hydroxyphenyl)prop-2-enoate 163188669 Click to see C1=CC(=CC=C1C=CC(=O)OC2C(C(C(OC2C3=C(C=CC4=C3OC(=CC4=O)C5=CC=C(C=C5)O)OC6C(C(C(C(O6)CO)O)O)O)CO)O)O)O 724.70 unknown https://doi.org/10.1016/0031-9422(95)00403-T

Biological Material Top ebay Auctions

Please wait .. loading items ..

Contributors Top

No known contributors. Be the first!

Collections Top

In private collections 0
In public collections 0
You need to be authenticated in order to add this taxon to a personal collection.