Fusarium avenaceum

(Fr.) Sacc. · species

image placeholder — illustration coming later

Fungi/Ascomycota/Sordariomycetes/Hypocreales/Nectriaceae/Fusarium

At a glance

Occurrence records520

Data sources9

Biological traits0

DNA specimens166

eDNA detections239

Sources9 archives

Databases and archives Fusarium avenaceum's data was compiled from.

WikipediaWikimedia Foundation6 languages↗

BioWikiNetmultilingual Wikipediamultilingual↗

GBIFGlobal Biodiversity Information Facility520 records↗

ENAEuropean Nucleotide Archive · EMBL-EBI239 eDNA detections↗

BOLD SystemsCentre for Biodiversity Genomics166 specimens↗

LOTUSNatural Products (Wikidata)compounds↗

GoaTGenomes on a Tree · Sangergenome & karyotype↗

Catalogue of LifeCOLtaxonomy↗

GLoBIGlobal Biotic Interactionsbiotic interactions↗

On this page6 sections

Every layer below draws on the sources above — open one to explore it, or use ← → to move between tabs.

NarrativeWikipediaarticle

Chemical compositionLOTUS15 compounds

Occurrence & distributionGBIF520 records

Environmental DNA3 datasets · 40 countries239 detections

DNA & barcodingBOLD166 specimens

Genome at a glanceGoaT≈42 Mbp

01Narrative

Gibberella avenacea is a fungal plant pathogen. Fusarium cortical stem rot

No narrative description available for this taxon yet.

02Traits & measurements

No structured trait data for this taxon yet.

03Chemical composition15 compounds

Compounds documented for Fusarium avenaceum across natural-product and food-composition databases — not just the ~150 nutrients on a classic label ("nutritional dark matter").

Compound class profile5 classes

Miscellaneous polyketides4

Cyclic peptides $ Depsipeptides4

Furans $ Miscellaneous polyketides1

Cyclonerane sesquiterpenoids1

2-pyrone derivatives1

Documented compounds15 total

Tissue Source Quantified only

Compound	Amount	Source
3,9,15-Tribenzyl-4,10,16-trimethyl-6,12,18-tri(propan-2-yl)-1,7,13-trioxa-4,10,16-triazacyclooctadecane-2,5,8,11,14,17-hexone	present	LOTUS
Acuminatopyrone	present	LOTUS
Beauvericin	present	LOTUS
cyclo[N(Me)Ile-D-OVal-N(Me)aIle-D-OVal-N(Me)Leu-D-OVal]	present	LOTUS
Cyclonerotriol B	present	LOTUS
Enniatin A2	present	LOTUS
Fosfonochlorin	present	LOTUS
Fusaravenin	present	LOTUS
Spiroleptosphol T1	present	LOTUS
Spiroleptosphol T2	present	LOTUS

05DNA & barcoding166 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 Fusarium avenaceum has left across the world's sequence archives.

At a glance

DNA specimens166

Marker genes4

eDNA detections239

Countries40

Marker genes sequenced

★ 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.

★COI-5P★ITS★ITS1★ITS2

animal barcodefungal barcode

06Genome at a glanceGoaT

The complete instruction manual Fusarium avenaceum 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

Genome size≈42 041 114 bp assembly estimate

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).

BACTERIUM Carsonella ruddii0.00016 Gb

FUNGUS0.04 Gb

THIS GENOME Fusarium avenaceum0.04 Gb

INSECT0.25 Gb

HUMAN3.2 Gb

WHEAT17 Gb

FERN Tmesipteris160.45 Gb

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.

Assembly levelComplete Genome

Completeness97.8% BUSCO

08Occurrence & distribution

Record type520 records

Wild obs. + sensor69

Museum / vouchered377

Cultivated / captive74

Range

Area of Occupancy AOO848 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 accuracy17% within 1 km

≤100 m 5≤1 km 6≤10 km 55

66 georeferenced · 3 without coordinates

Open the mapobservation + sensor69

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 accuracy41% within 1 km

≤100 m 4≤1 km 14≤10 km 20>10 km 6

44 georeferenced · 333 without coordinates

Open the institutions mapphysical evidence377

Cultivated / Captivenot free-living

A living individual in a botanical garden, zoo or nursery — cultivated or kept, not free-living.

Coordinate accuracy0% within 1 km

>10 km 3

3 georeferenced · 71 without coordinates

Open the mapnot free-living74

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 institutions7 of 17 geolocated

Institutions and collections holding physical, vouchered specimens of this species — click a row to fly to it on the map.

Institution	Specimens
DPIlocation not on record	48
Tartu, EE	12
ILLSlocation not on record	12
CA	10
Uppsala, SE	6
Agriculture and Agri-Food Canada, Canadian National Mycological Herbariumlocation not on record	5
Bernard Price Institute for Palaeontological Researchlocation not on record	5
Pullman, US	3
Agriculture and Agri-Food Canadalocation not on record	2
Helsinki, FI	2
Kensington, AU	1
Uniwersytet Marii Curie-Skłodowskiejlocation not on record	1
Museo Entomologico de Leonlocation not on record	1
UAclocation not on record	1
Auckland, NZ	1
Catholic University of Pekinglocation not on record	1
Institute of Botany of the Academy of Sciences of the Republic of Uzbekistanlocation not on record	1

17 institutions · 112 of 377 vouchered records shown · 256 without an institution code

Cultivated / Captivenot free-living

A living individual in a botanical garden, zoo or nursery — cultivated or kept, not free-living.

09Environmental DNA239 detections

Where the DNA of Fusarium avenaceum 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 found239

Studies independent surveys3

Countries40

Signal confidence: moderateweighed across independent studies, places & mapped detections

Where its DNA was found

0 of 239 detections have coordinates

Open the map40 countries0

IndomalayanAfrotropicPalearcticNearcticNeotropicAustralasia

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.

Modelled climatemodelled

−15°Ctemperature across detection sites+40°C

Temperature median9.80 °C -0.5–18.2

Seasonal swing summer↔winter19.2 °C

Max temp (day)14.3 °C 1.80–23.5

Min temp (night)5.40 °C -4.90–14.4

Precipitation80.1 mm/mo 43.8–246

Air humidity60.3 % 52.7–66.7

Moisture balance14.3 mm/mo -60.7–263

Vapour deficit527 Pa 227–983

Wind speed3.10 m/s 1.80–6.00

Cloud cover39.8 % 25.4–53.7

CHELSA 1981–2010, ~9 km grid, at location & month of 93 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.

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