Auriscalpium vulgare
Gray · speciesAt a glance
Sources10 archives
Databases and archives Auriscalpium vulgare's data was compiled from.
WikipediaWikimedia Foundation12 languages↗
BioWikiNetmultilingual Wikipediamultilingual↗
GBIFGlobal Biodiversity Information Facility18 893 records↗
ENAEuropean Nucleotide Archive · EMBL-EBI140 eDNA detections↗
BOLD SystemsCentre for Biodiversity Genomics14 specimens↗
NCBIUS National Library of Medicinesequences↗
Open Tree of LifeOpenTreephylogeny backbone↗
GoaTGenomes on a Tree · Sangergenome & karyotype↗
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.
Auriscalpium vulgare, commonly known as the pinecone mushroom, the cone tooth, or the ear-pick fungus, is a species of fungus in the family Auriscalpiaceae of the order Russulales. It was first described in 1753 by Carl Linnaeus, who included it as a member of the tooth fungi genus Hydnum, but British mycologist Samuel Frederick Gray recognized its uniqueness and in 1821 transferred it to the genus Auriscalpium that he created to contain it. The fungus is widely distributed in Europe, Central America, North America, and temperate Asia. Although common, its small size and nondescript colors lead it to be easily overlooked in the pine woods where it grows. A. vulgare is not generally considered edible because of its tough texture, but some historical literature says it used to be consumed in France and Italy. The fruit bodies (mushrooms) grow on conifer litter or on conifer cones that may be partially or completely buried in soil. The dark brown cap of the small, spoon-shaped mushroom is covered with fine brown hairs, and reaches a diameter of up to 2 cm. On the underside of the cap are a crowded array of tiny tooth-shaped protrusions ("teeth") up to 3 mm long; they are initially whitish to purplish-pink before turning brown in age. The dark brown and hairy stem, up to 55 mm long and 2 mm thick, attaches to one edge of the cap. The mushroom produces a white spore print out of roughly spherical spores. High levels of humidity are essential for optimum fruit body development, and growth is inhibited by either too much or too little light. Fruit bodies change their geotropic response three times during their development, which helps ensure that the teeth ultimately point downward for optimum spore release. The pure culture, cell division and the ultrastructure of A. vulgares hyphae and mycelia have been studied and described in search of potentially useful characters for phylogenetic analysis. When grown in culture, the fungus can be induced to produce fruit bodies under suitable conditions.
No narrative description available for this taxon yet.
No structured trait data for this taxon yet.
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 Auriscalpium vulgare 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 Auriscalpium vulgare 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).
Sequencing statusassembly quality — how far to trust these numbers
Assembly level tells you how finished the sequence is — from fragmented contigs, through scaffolds, up to a full chromosome-level assembly. BUSCO % estimates completeness: the share of genes expected to be present that were actually found. These describe the data quality, not the organism.
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 type18 893 records
Origin
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 institutions55 of 105 geolocated
Institutions and collections holding physical, vouchered specimens of this species — click a row to fly to it on the map.
| Institution | Specimens |
|---|---|
| Helsinki, FI | 230 |
| Olocation not on record | 134 |
| Zapopan, MX | 62 |
| Tartu, EE | 47 |
| Karlsruhe, DE | 43 |
| Mexico City, MX | 42 |
| Uppsala, SE | 41 |
| Adam Mickiewicz University in Poznańlocation not on record | 36 |
| TENN-Flocation not on record | 35 |
| BDBClocation not on record | 33 |
| GJOlocation not on record | 31 |
| Copenhagen, DK | 31 |
| Toronto, CA | 27 |
| Kew, GB | 23 |
| WTUlocation not on record | 23 |
| Joensuu, FI | 22 |
| Trondheim, NO | 22 |
| SLU Artdatabankenlocation not on record | 21 |
| St. Paul, US | 20 |
| Görlitz, DE | 20 |
| Durango, MX | 19 |
| Pullman, US | 19 |
| San Sebastián, ES | 18 |
| Philadelphia, US | 17 |
| Kuopio, FI | 16 |
| Chicago, US | 16 |
| Entomological Society of Latvialocation not on record | 14 |
| Université de Montréal Biodiversity Centrelocation not on record | 13 |
| Jyväskylä, FI | 11 |
| WU-MYClocation not on record | 11 |
| Ciudad de México, MX | 10 |
| Ann Arbor, US | 10 |
| Zürich, CH | 10 |
| Vancouver, CA | 9 |
| Museo Entomologico de Leonlocation not on record | 9 |
| Uniwersytet Łódzkilocation not on record | 8 |
| Mexico City, MX | 8 |
| MeiseBGlocation not on record | 8 |
| ILLSlocation not on record | 8 |
| MAlocation not on record | 8 |
| Salzburg, AT | 7 |
| Warsaw, PL | 7 |
| Museum Ludovicae Ulricae, Zoology Institute of the University of Uppsalalocation not on record | 7 |
| Göteborg, SE | 7 |
| Cincinnati, US | 7 |
| IFR-DNFlocation not on record | 6 |
| LDlocation not on record | 6 |
| CA | 5 |
| National Mushroom Centre, Department of Agriculture, Ministry of Agriculture and Livestock, Bhutanlocation not on record | 5 |
| Staten Island, US | 5 |
| nsnflocation not on record | 5 |
| University of the Basque Country (UPV/EHU)location not on record | 5 |
| Mlocation not on record | 5 |
| Universidade de Lisboa, Museu Bocagelocation not on record | 5 |
| Museo civico di Storia naturale Giacomo Doria di Genova | Giacomo Doria Natural History Museum in Genoalocation not on record | 5 |
| Berlin, DE | 4 |
| Bardejov, SK | 4 |
| California State University, East Baylocation not on record | 3 |
| Osaka, JP | 3 |
| JA-CAGPDS-CAMlocation not on record | 3 |
| Bernard Price Institute for Palaeontological Researchlocation not on record | 3 |
| Vitoria, ES | 3 |
| Bando, JP | 3 |
| UNINE:NEUlocation not on record | 3 |
| McWane Science Centerlocation not on record | 3 |
| Denver, US | 2 |
| Durham, US | 2 |
| Champaign, US | 2 |
| Baton Rouge, US | 2 |
| V. N. Karazin National Universitylocation not on record | 2 |
| Madison, US | 2 |
| Stockholm, SE | 2 |
| Winterthur, CH | 2 |
| Tilburg, NL | 2 |
| Oulu, FI | 2 |
| Uniwersytet Marii Curie-Skłodowskiejlocation not on record | 2 |
| Chiba, JP | 2 |
| CJBGlocation not on record | 2 |
| Acadia Universitylocation not on record | 2 |
| University of Oslo, Natural History Museumlocation not on record | 1 |
| FLASlocation not on record | 1 |
| Oskarshamn, SE | 1 |
| Turku, FI | 1 |
| Slovenian Forestry Institutelocation not on record | 1 |
| Youngstown State Universitylocation not on record | 1 |
| Catholic University of Pekinglocation not on record | 1 |
| Gijón, ES | 1 |
| DPIlocation not on record | 1 |
| Royal Botanic Gardens, Kewlocation not on record | 1 |
| Fort Hayslocation not on record | 1 |
| Natural History Museum Rotterdamlocation not on record | 1 |
| University of Tennessee at Chattanoogalocation not on record | 1 |
| Provincia di Livornolocation not on record | 1 |
| Bronx, US | 1 |
| Salamanca, ES | 1 |
| Department of Plant Resources, National Herbarium and Plant Laboratorieslocation not on record | 1 |
| National Institute of Biological Resourceslocation not on record | 1 |
| Odawara, JP | 1 |
| Mexico City, MX | 1 |
| Santa Cruz, US | 1 |
| Davis and Elkins Collegelocation not on record | 1 |
| TROMlocation not on record | 1 |
| BRNUlocation not on record | 1 |
| US | 1 |
| TUR-Alocation not on record | 1 |
Where the DNA of Auriscalpium vulgare 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.