Aspergillus sulphureus

(Fresen.) Thom & Church · species

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Fungi/Ascomycota/Eurotiomycetes/Eurotiales/Trichocomaceae/Aspergillus

At a glance

Occurrence records3

Data sources6

Biological traits0

DNA specimens6

eDNA detections6

Sources6 archives

Databases and archives Aspergillus sulphureus's data was compiled from.

BioWikiNetmultilingual Wikipediamultilingual↗

GBIFGlobal Biodiversity Information Facility3 records↗

ENAEuropean Nucleotide Archive · EMBL-EBI6 eDNA detections↗

BOLD SystemsCentre for Biodiversity Genomics6 specimens↗

LOTUSNatural Products (Wikidata)compounds↗

GLoBIGlobal Biotic Interactionsbiotic interactions↗

On this page5 sections

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

NarrativeWikipediaarticle

Chemical compositionLOTUS33 compounds

Occurrence & distributionGBIF3 records

Environmental DNA1 datasets · 1 countries6 detections

DNA & barcodingBOLD6 specimens

01Narrative

硫色曲霉是属于散囊菌目发菌科曲霉属的一种真菌，可生长在土壤、南瓜子、越冬三化螟、黑尾叶蝉等基物上。该种分布于中国、印度、巴哈马、加纳、以色列、意大利、美国等地。

No narrative description available for this taxon yet.

02Traits & measurements

No structured trait data for this taxon yet.

03Chemical composition33 compounds

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

Compound class profile5 classes

Indole diketopiperazine alkaloids (L-Trp, L-Pro)12

Indole-Diterpenoid alkaloids (Penitrems)10

Miscellaneous meroterpenoids6

Cyclic peptides $ Depsipeptides1

Fungal DPEs $ Simple aromatic polyketides1

Documented compounds33 total

Tissue Source Quantified only

Compound	Amount	Source
(1R,4aS,4bS,7R,8S,8aS,10aS)-8-(6-hydroxy-1H-indol-3-yl)-1,4b,7,8,10a-pentamethyl-1,3,4,4a,5,6,7,8a,9,10-decahydrophenanthren-2-one	present	LOTUS
(1S,2R,5S,6R,8R,9S,10R,12S,15R,16S,24R,25S,27S,28S)-5,9-dihydroxy-15,16,24,33,33-pentamethyl-10-prop-1-en-2-yl-7,11,32-trioxa-18-azadecacyclo[25.4.2.02,16.05,15.06,8.06,12.017,31.019,30.022,29.025,28]tritriaconta-17(31),19(30),20,22(29)-tetraen-23-one	present	LOTUS
(1S,2R,5S,7R,8S,9R,11R,12R,15S)-1,2-dimethyl-21-(2-methylbut-3-en-2-yl)-7-prop-1-en-2-yl-6,10-dioxa-24-azaheptacyclo[13.10.0.02,12.05,11.09,11.017,25.018,23]pentacosa-17(25),18(23),19,21-tetraene-8,12-diol	present	LOTUS
(1S,2R,5S,7R,8S,9R,11R,12S,15S)-8,12-dihydroxy-1,2-dimethyl-21-(2-methylbut-3-en-2-yl)-7-prop-1-en-2-yl-6,10-dioxa-24-azahexacyclo[13.10.0.02,12.05,11.09,11.018,23]pentacosa-18(23),19,21-triene-17,25-dione	present	LOTUS
(1S,2R,5S,7R,8S,9R,11S,12S,15R)-1,2-dimethyl-21-(2-methylbut-3-en-2-yl)-7-prop-1-en-2-yl-6,10-dioxa-24-azaheptacyclo[13.10.0.02,12.05,11.09,11.017,25.018,23]pentacosa-17(25),18(23),19,21-tetraene-8,12-diol	present	LOTUS
(2S,3R,6S,8R,9S,10R,12R,13S,16S,21R,22S,24S)-22-(2-hydroxypropan-2-yl)-2,3-dimethyl-25-methylidene-8-prop-1-en-2-yl-7,11-dioxa-31-azanonacyclo[16.13.0.02,16.03,13.06,12.010,12.019,30.020,27.021,24]hentriaconta-1(18),19(30),20(27),28-tetraene-9,13-diol	present	LOTUS
(3S)-3-[[(3R)-7,7-dimethyl-3-(2-methylbut-3-en-2-yl)-2-oxo-1H-pyrano[2,3-g]indol-3-yl]methyl]-8a-hydroxy-3,6,7,8-tetrahydro-2H-pyrrolo[1,2-a]pyrazine-1,4-dione	present	LOTUS
(S)-3-(((S)-7,7-Dimethyl-3-(2-methylbut-3-en-2-yl)-2-oxo-1,2,3,7-tetrahydropyrano[2,3-g]indol-3-yl)methyl)-2,3,6,7-tetrahydropyrrolo[1,2-a]pyrazine-1,4-dione	present	LOTUS
10-O-acetylsclerotiamide	present	LOTUS
10-O-ethylnotoamide R	present	LOTUS

05DNA & barcoding6 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 Aspergillus sulphureus has left across the world's sequence archives.

At a glance

DNA specimens6

Marker genes1

eDNA detections6

Countries1

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.

★ITS

fungal barcode

08Occurrence & distribution

Record type3 records

Museum / vouchered3

Range

Area of Occupancy AOO8 km²

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 accuracy0% within 1 km

≤10 km 1

1 georeferenced · 2 without coordinates

Open the institutions mapphysical evidence3

10Collections & institutions

Institution	Specimens
Annamalai University, Centre of Advanced Study in Marine Biologylocation not on record	2
Bernard Price Institute for Palaeontological Researchlocation not on record	1

2 institutions · 3 of 3 vouchered records shown

09Environmental DNA6 detections

Where the DNA of Aspergillus sulphureus 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 found6

Studies independent surveys1

Countries1

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

Where its DNA was found

0 of 6 detections have coordinates

Open the map1 country0

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 median25.1 °C 25.1–25.1

Seasonal swing summer↔winter16.5 °C

Max temp (day)30.5 °C

Min temp (night)19.3 °C

Precipitation109 mm/mo

Air humidity52.0 %

Moisture balance-17.8 mm/mo

Vapour deficit1,616 Pa

Wind speed1.80 m/s

Cloud cover25.2 %

CHELSA 1981–2010, ~9 km grid, at location & month of 2 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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