Ramaria botrytis, commonly known as the clustered coral, the pink-tipped coral mushroom, or the cauliflower coral, is an edible species of coral fungus in the family Gomphaceae. Its robust fruit body can grow up to 15 cm in diameter and 20 cm tall, and resembles some marine coral. Its dense branches, which originate from a stout, massive base, are swollen at the tips and divided into several small branchlets. The branches are initially whitish but age to buff or tan, with tips that are pink to reddish. The flesh is thick and white. The spores, yellowish in deposit, are ellipsoid, feature longitudinal striations, and measure about 13.8 by 4.7 micrometers. The type species of the genus Ramaria, R. botrytis was first described scientifically in 1797 by mycologist Christiaan Hendrik Persoon. A widely distributed species, it is found in North America, North Africa, central and eastern Europe, Australia, and Asia. The fungus is mycorrhizal with broadleaf trees, and fruits on the ground in wooded areas. There are several species of coral fungi that are superficially similar in appearance to R. botrytis, and although comparison of habitat or characteristics like color or branching morphology is often sufficient for identification, sometimes microscopy is required to definitively distinguish between them. Fruit bodies of Ramaria botrytis are edible, and young specimens have a mild, fruity taste. Some authors warn of laxative effects in susceptible individuals. The fungus contains several chemical compounds with in vitro biological activity, and fruit bodies have antimicrobial activity against several species and strains of drug-resistant bacteria that cause disease in humans.
No narrative description available for this taxon yet.
Compounds documented for Ramaria botrytis across natural-product and food-composition databases — not just the ~150 nutrients on a classic label ("nutritional dark matter").
Compound class profile2 classes
Cholestane steroids $ Ergostane steroids2
Ergostane steroids1
Documented compounds3 total
Compound
Class
Amount
Source
3beta,5alpha,6beta-Trihydroxy-7,22-ergostadiene
present
LOTUS
Ergosterol
present
LOTUS
Ergosterol Peroxide
present
LOTUS
05DNA & barcoding23 specimens
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 Ramaria botrytis has left across the world's sequence archives.
At a glance
DNA specimens23
Marker genes2
GenBank sequences10
eDNA detections32
Countries8
The DNA barcodea real sequence read deposited for this species
★ 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.
★ITS10★ITS1
fungal barcode
08Occurrence & distribution
Record type2 979 records
Wild obs. + sensor2 562
Museum / vouchered417
Origin
Native28
Range
Area of Occupancy AOO6 064 km²
Wildobservation + sensor
Human sightings and records, or camera-trap / sensor detections — someone (or a device) saw or captured the species in the wild.
Coordinate accuracy86% within 1 km
≤100 m 1 637≤1 km 462≤10 km 314>10 km 39
2 452 georeferenced · 110 without coordinates
Open the mapobservation + sensor2 562
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.
Coordinate accuracy75% within 1 km
≤100 m 132≤1 km 71≤10 km 41>10 km 28
272 georeferenced · 145 without coordinates
Open the institutions mapphysical evidence417
Wildobservation + sensor
Human sightings and records, or camera-trap / sensor detections — someone (or a device) saw or captured the species in the wild.
10Collections & institutions
Holding institutions25 of 48 geolocated
Institutions and collections holding physical, vouchered specimens of this species — click a row to fly to it on the map.
Institution
Specimens
Olocation not on record
98
TENN-Flocation not on record
61
SLU Artdatabankenlocation not on record
51
Uppsala, SE
24
MAlocation not on record
15
San Sebastián, ES
9
nsnflocation not on record
9
Bardejov, SK
8
Bernard Price Institute for Palaeontological Researchlocation not on record
8
Osaka, JP
7
LDlocation not on record
7
Copenhagen, DK
7
University of Oslo, Natural History Museumlocation not on record
7
Denver, US
7
Davis and Elkins Collegelocation not on record
6
Vancouver, CA
6
Göteborg, SE
6
Cincinnati, US
6
Trondheim, NO
5
BioFokuslocation not on record
5
Norwegian Institute for Nature Researchlocation not on record
4
Staten Island, US
3
Turku, FI
3
TUR-Alocation not on record
3
Helsinki, FI
3
ILLSlocation not on record
3
Kuopio, FI
3
Umeå Universitylocation not on record
2
Kathmandu, NP
2
Kew, GB
2
Blacksburg, US
2
JA-CAGPDS-CAMlocation not on record
2
MFUlocation not on record
2
Toronto, CA
1
McWane Science Centerlocation not on record
1
FLASlocation not on record
1
Provincia di Livornolocation not on record
1
Champaign, US
1
Private Collection of Steve Nesslocation not on record
1
Department of Plant Resources, National Herbarium and Plant Laboratorieslocation not on record
1
Ann Arbor, US
1
Joensuu, FI
1
Durham, US
1
Clemson, US
1
California State University, East Baylocation not on record
1
Personal Herbarium of Steve Nesslocation not on record
1
Baton Rouge, US
1
Berlin, DE
1
48 institutions · 401 of 417 vouchered records shown · 12 without an institution code
09Environmental DNA32 detections
Where the DNA of Ramaria botrytis 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
Detections DNA found32
Studies independent surveys5
Countries7
Verifiable raw sequence linked2
Signal confidence: moderateweighed across independent studies, places & mapped detections
Where its DNA was found
0 of 32 detections have coordinates
Open the map7 countries0
In rich spruce forestMontane old growth conifer forest
How strong is each trace?
DNA read depthRead counts were not reported for this species — the map shows presence only, not how strong each trace was.
Measured at samplingin-field
Depth0 m
SoilKurosol
1 sample with on-site data · median with range · describes the sample, not the organism
Modelled climatemodelled
−15°Ctemperature across detection sites+40°C
Temperature median13.1 °C 9.10–21.5
Seasonal swing summer↔winter17.1 °C
Max temp (day)16.5 °C 11.6–25.9
Min temp (night)9.00 °C 5.10–17.4
Precipitation154 mm/mo 81.3–207
Air humidity63.2 % 53.9–66.0
Moisture balance53.0 mm/mo -25.1–163
Vapour deficit606 Pa 421–928
Wind speed2.00 m/s 1.70–3.40
Cloud cover47.7 % 37.9–50.7
CHELSA 1981–2010, ~9 km grid, at location & month of 24 detection points · median with p10–p90 · reflects where sampling happened, not only the true niche
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.