Tapinella atrotomentosa
(Batsch) Šutara · speciesAt a glance
Sources9 archives
Databases and archives Tapinella atrotomentosa's data was compiled from.
WikipediaWikimedia Foundation12 languages↗
BioWikiNetmultilingual Wikipediamultilingual↗
GBIFGlobal Biodiversity Information Facility23 562 records↗
ENAEuropean Nucleotide Archive · EMBL-EBI651 eDNA detections↗
BOLD SystemsCentre for Biodiversity Genomics18 specimens↗
LOTUSNatural Products (Wikidata)compounds↗
GoaTGenomes on a Tree · Sangergenome ~0.05 Gbp↗
Catalogue of LifeCOLtaxonomy↗
GLoBIGlobal Biotic Interactionsbiotic interactions↗Every layer below draws on the sources above — open one to explore it, or use ← → to move between tabs.
Tapinella atrotomentosa, commonly known as the velvet roll-rim or velvet-footed pax, is a species of fungus in the family Tapinellaceae. Although it has gills, it is a member of the pored mushroom order Boletales. August Batsch described the species in 1783. It has been recorded from Asia, Central America, Europe and North America. Tough and inedible, it grows on tree stumps of conifers. The mushroom contains several compounds that act as deterrents of feeding by insects.
No narrative description available for this taxon yet.
No structured trait data for this taxon yet.
Compounds documented for Tapinella atrotomentosa across natural-product and food-composition databases — not just the ~150 nutrients on a classic label ("nutritional dark matter").
Compound class profile5 classes
Documented compounds40 total
| Compound | Class | Amount | Source |
|---|---|---|---|
| (2E)-2-(3,4-dihydroxyphenyl)-3,4-dihydroxy-5-(4-hydroxyphenyl)hexa-2,4-dienedioic acid | present | LOTUS | |
| (2S,3R,5R,9R,10R,11R,13R,14S,17S)-17-[(2R,3R,5R)-2,3-dihydroxy-5,6-dimethylheptan-2-yl]-2,3,11,14-tetrahydroxy-10,13-dimethyl-2,3,4,5,9,11,12,15,16,17-decahydro-1H-cyclopenta[a]phenanthren-6-one | present | LOTUS | |
| (2S,3R,5R,9R,10R,11R,13R,14S,17S)-2,3,11,14-tetrahydroxy-10,13-dimethyl-17-[(2R,3R,5R)-2,3,5-trihydroxy-5,6-dimethylheptan-2-yl]-2,3,4,5,9,11,12,15,16,17-decahydro-1H-cyclopenta[a]phenanthren-6-one | present | LOTUS | |
| (2S,3R,5R,9R,10R,11R,13R,14S,17S)-2,3,11,14-tetrahydroxy-10,13-dimethyl-17-[(2R,3R,5R)-2,3,6-trihydroxy-5,6-dimethylheptan-2-yl]-2,3,4,5,9,11,12,15,16,17-decahydro-1H-cyclopenta[a]phenanthren-6-one | present | LOTUS | |
| (2S,3R,5R,9R,10R,11R,13R,14S,17S)-2,3,11,14-tetrahydroxy-10,13-dimethyl-17-[(2R,3R,5S)-2,3,6-trihydroxy-5,6-dimethylheptan-2-yl]-2,3,4,5,9,11,12,15,16,17-decahydro-1H-cyclopenta[a]phenanthren-6-one | present | LOTUS | |
| (2S,3R,5R,9R,10R,11R,13R,14S,17S)-2,3,11,14-tetrahydroxy-17-[(1R)-1-hydroxy-1-[(2R,3R)-3-[(2R)-3-hydroxy-3-methylbutan-2-yl]oxiran-2-yl]ethyl]-10,13-dimethyl-2,3,4,5,9,11,12,15,16,17-decahydro-1H-cyclopenta[a]phenanthren-6-one | present | LOTUS | |
| (2S,3R,5R,9R,10R,11R,13R,14S,17S)-2,3,11,14-tetrahydroxy-17-[(1R)-1-hydroxy-1-[(2R,3R)-3-[(2R)-3-methylbutan-2-yl]oxiran-2-yl]ethyl]-10,13-dimethyl-2,3,4,5,9,11,12,15,16,17-decahydro-1H-cyclopenta[a]phenanthren-6-one | present | LOTUS | |
| (2S,3R,5R,9R,10R,11R,13R,14S,17S)-2,3,11,14-tetrahydroxy-17-[(2S,4R,5R)-5-[(2S)-2-hydroxy-2,3-dimethylbutyl]-2-(4-hydroxyphenyl)-4-methyl-1,3-dioxolan-4-yl]-10,13-dimethyl-2,3,4,5,9,11,12,15,16,17-decahydro-1H-cyclopenta[a]phenanthren-6-one | present | LOTUS | |
| (3R*,4S*,5S*)-3-Acetoxy-5-hydroxyhexan-4 | present | LOTUS | |
| (3Z,5S,6R,9Z,11S,12R)-5,11-dihydroxy-6,12-dimethyl-1,7-dioxacyclododeca-3,9-diene-2,8-dione | present | LOTUS |
A DNA barcode is a short, standardised stretch of genes that works like a fingerprint — enough to tell one species from another. Below is the molecular trace Tapinella atrotomentosa has left across the world's sequence archives.
At a glance
★ the standard DNA barcode for this group — the short region actually read to tell this species apart. The rest are extra genes sequenced along the way.
The complete instruction manual Tapinella atrotomentosa carries — its genome. We read it from three angles — how big it is, how the DNA is packed into chromosomes, and how completely it has been sequenced — and explain how to read each value as you go.
Genome sizehow big the whole instruction manual is
Measured in base pairs (bp) — the individual letters of DNA (human ≈ 3.2 Gb, a bacterium a few million). The chart places this genome on a logarithmic scale — each step to the right is ten times bigger — among reference organisms. Across species a bigger genome loosely tracks with larger cells, slower growth and lower-energy lifestyles (powered flight favours small genomes) — yet it does not imply more genes or a more advanced organism (the long-standing C-value paradox).
How far back this lineage goes — and how we know. Everything here is measured in Ma, short for “mega-annum”: millions of years ago. The chart reads left to right like a calendar of the Earth, from the deep past on the left to today at the right edgetop to bottom like a core drilled through the Earth, from the deep past at the top down to today at the bottom.
At a glance
When this lineage existed
How to read this: the coloured strip along the bottomdown the left is the geological calendar — the standard epochs (Pliocene, Pleistocene…) every museum uses, shown so you can see which chapter of Earth's history this lineage lived in. This lineage is a young one, so the strip is zoomed in to epochs — the finer subdivisions inside a period. The orange marker is the DNA clock: DNA accumulates mutations at a roughly steady rate, so comparing this species' DNA with its relatives estimates when the lineage split off — independently of any fossil.
Record type23 562 records
Range
Wildobservation + sensor
Human sightings and records, or camera-trap / sensor detections — someone (or a device) saw or captured the species in the wild.
Museum / Voucheredphysical evidence
Backed by a physical specimen — a herbarium sheet, sample or voucher held in a collection. “Vouchered” means supported by material evidence, not just an observation.
Wildobservation + sensor
Human sightings and records, or camera-trap / sensor detections — someone (or a device) saw or captured the species in the wild.
Holding institutions42 of 73 geolocated
Institutions and collections holding physical, vouchered specimens of this species — click a row to fly to it on the map.
| Institution | Specimens |
|---|---|
| Joensuu, FI | 46 |
| Olocation not on record | 45 |
| Oulu, FI | 24 |
| BDBClocation not on record | 22 |
| Osaka, JP | 21 |
| Helsinki, FI | 20 |
| Kew, GB | 19 |
| Chicago, US | 15 |
| Trondheim, NO | 13 |
| Görlitz, DE | 13 |
| TENN-Flocation not on record | 11 |
| Philadelphia, US | 10 |
| Karlsruhe, DE | 10 |
| Université de Montréal Biodiversity Centrelocation not on record | 7 |
| San Sebastián, ES | 7 |
| Vitoria, ES | 6 |
| Göteborg, SE | 5 |
| Museum Ludovicae Ulricae, Zoology Institute of the University of Uppsalalocation not on record | 5 |
| WTUlocation not on record | 5 |
| Kuopio, FI | 5 |
| Warsaw, PL | 5 |
| WU-MYClocation not on record | 4 |
| Universidade de Lisboa, Museu Bocagelocation not on record | 4 |
| Acadia Universitylocation not on record | 3 |
| Kathmandu, NP | 3 |
| University of Oslo, Natural History Museumlocation not on record | 3 |
| LDlocation not on record | 3 |
| Tartu, EE | 3 |
| SLU Artdatabankenlocation not on record | 3 |
| St. Paul, US | 3 |
| National Mushroom Centre, Department of Agriculture, Ministry of Agriculture and Livestock, Bhutanlocation not on record | 3 |
| Auckland, NZ | 3 |
| Uniwersytet Łódzkilocation not on record | 3 |
| Salzburg, AT | 2 |
| GJOlocation not on record | 2 |
| Copenhagen, DK | 2 |
| Vancouver, CA | 2 |
| Santa Cruz, US | 2 |
| Stockholm, SE | 2 |
| Bardejov, SK | 2 |
| Museo civico di Storia naturale Giacomo Doria di Genova | Giacomo Doria Natural History Museum in Genoalocation not on record | 2 |
| Senckenberg Gesellschaft für Naturforschung: Senckenberg Forschungsinstitut und Naturmuseumlocation not on record | 1 |
| Catholic University of Pekinglocation not on record | 1 |
| Toyota city nature sanctuarylocation not on record | 1 |
| Turku, FI | 1 |
| Tampa, US | 1 |
| FLASlocation not on record | 1 |
| Tomioka, JP | 1 |
| Ann Arbor, US | 1 |
| Natural History Museum Rotterdamlocation not on record | 1 |
| Uppsala, SE | 1 |
| Research Collection of Steve Nesslocation not on record | 1 |
| Bando, JP | 1 |
| Denver, US | 1 |
| Private Collection of Autumn Anglinlocation not on record | 1 |
| Gijón, ES | 1 |
| California State University, East Baylocation not on record | 1 |
| Yerevan, AM | 1 |
| Staten Island, US | 1 |
| Cornell University, Plant Pathology Herbariumlocation not on record | 1 |
| Royal Ontario Museum, TRTC Fungariumlocation not on record | 1 |
| Natural History Museum, Tribhuvan Universitylocation not on record | 1 |
| IB FRC Komi SC UB RASlocation not on record | 1 |
| Zürich, CH | 1 |
| nsnflocation not on record | 1 |
| Oskarshamn, SE | 1 |
| Odawara, JP | 1 |
| Bronx, US | 1 |
| CJBGlocation not on record | 1 |
| Valdosta State Universitylocation not on record | 1 |
| Mexico City, MX | 1 |
| Durham, US | 1 |
| Asheville, US | 1 |
Where the DNA of Tapinella atrotomentosa was picked up in samples of water, soil or air — nobody saw the organism, only its DNA left behind. A trace is a clue that the species was near, not a confirmed sighting.
Signal
Where its DNA was found
How strong is each trace?
Measured at samplingin-field
Modelled climatemodelled
How to read this: each dot is one detection of this species' DNA in an environmental sample. The confidence meter weighs how many independent studies and places back up the signal — one detection in one study is a hint; many across several studies is solid. Records dated before 2008 (when eDNA methods began) are treated as likely mislabeled and left off the map.