Angerona is a monotypic moth genus in the family Geometridae erected by Philogène Auguste Joseph Duponchel in 1829. Its only species, Angerona prunaria, the orange moth, was first described by Carl Linnaeus in his 1758 10th edition of Systema Naturae.
No narrative description available 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 Angerona prunaria has left across the world's sequence archives.
At a glance
DNA specimens75
BINs3
Marker genes3
eDNA detections68
Countries13
The DNA barcodethe species' typical barcode, built from every sequenced specimen
COI-5P658 bp consensus64 specimens
ACGT
▸ drag or hover over the strip to read any position — letter and how much it varies
Violet ticks below the strip = positions where individuals differ; flat = the species' unchanging signature. 98% of positions are identical in every specimen.
Where individuals differ — all 16 variable positions, in barcode order
Each circle is a barcode variant; bigger = more specimens, colour = region. Lines join the most similar variants and the tick marks count the mutations between them — a tight cluster is one “dialect”, a long line a more divergent lineage. Click a circle to list its actual specimens.
Diversity (π)1.2%
Haplotypes15
BINs3
Most divergent pair2.6%
EuropeAsia
Closest relatives by DNA barcode
The species whose COI barcode is most similar to this one — a quick “who is this most like”. The percentage is how much the barcode differs; it approximates, but is not, the full evolutionary tree.
★ 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-3P★COI-5PEF1-alpha
animal barcodemarker
06Genome at a glanceGoaT · NCBI
The complete instruction manualAngerona prunaria 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≈348 594 942 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
INSECT0.25 Gb
THIS GENOME Angerona prunaria0.35 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.
Human sightings and records, or camera-trap / sensor detections — someone (or a device) saw or captured the species in the wild.
Coordinate accuracy52% within 1 km
≤100 m 9 523≤1 km 4 995≤10 km 13 064>10 km 178
27 760 georeferenced · 3 307 without coordinates
Open the mapobservation + sensor31 067
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 accuracy43% within 1 km
≤100 m 1 483≤1 km 1 524≤10 km 3 259>10 km 694
6 960 georeferenced · 2 002 without coordinates
Open the institutions mapphysical evidence8 962
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 institutions22 of 68 geolocated
Institutions and collections holding physical, vouchered specimens of this species — click a row to fly to it on the map.
Institution
Specimens
South Kensington, GB
1 636
DanishLepidopterologicalSocietylocation not on record
1 377
Helsinki, FI
1 156
Provincia di Livornolocation not on record
741
Zürich, CH
629
Museum Ludovicae Ulricae, Zoology Institute of the University of Uppsalalocation not on record
286
Bern, CH
262
Tartu, EE
157
Naturama Aargaulocation not on record
128
Salzburg, AT
123
Dhaka, BD
119
Kuopio, FI
112
Geneva, CH
97
Paro, BT
85
Philadelphia, US
80
NHMOlocation not on record
76
Archäologie und Museum Baselland - Museum.BLlocation not on record
76
Glarus, CH
76
ZMAAlocation not on record
71
Frauenfeld, CH
67
Adam Mickiewicz University in Poznańlocation not on record
56
Naturmuseum Solothurnlocation not on record
55
Podgorica, ME
47
Muzeum Górnośląskie w Bytomiulocation not on record
41
SLU Artdatabankenlocation not on record
40
Natural History Museum Rotterdamlocation not on record
39
Tallinn, EE
29
MUZOO - Musée d'histoire naturelle de La Chaux-de-Fondslocation not on record
22
Musee d'Histoire Naturallelocation not on record
20
Durban Natural Science Museumlocation not on record
19
Nijmegen, NL
19
Universität Zürich, Naturhistorisches Museumlocation not on record
18
Uniwersytet Łódzkilocation not on record
15
ZSMlocation not on record
14
Museum zu Allerheiligen Schaffhausenlocation not on record
13
HUNMlocation not on record
12
NCMGlocation not on record
11
DABUHlocation not on record
11
NSMKlocation not on record
10
Fribourg, CH
10
Naturmuseum St. Gallenlocation not on record
9
SFRAlocation not on record
9
John May Museum of Natural Historylocation not on record
8
Museo civico di Storia naturale Giacomo Doria di Genova | Giacomo Doria Natural History Museum in Genoalocation not on record
7
MZLUlocation not on record
6
NTNU-VMlocation not on record
5
Rovaniemi, FI
5
KSSlocation not on record
4
Maduka University Ekwegbe Nsukka Nigerialocation not on record
4
Naturmuseum Oltenlocation not on record
4
Bavarian State Collection of Zoologylocation not on record
4
Brussels, BE
4
Musée de Saint-Imierlocation not on record
4
Radicondoli, IT
3
Philosophical Societylocation not on record
3
Ugentlocation not on record
3
Cleveland Museum of Natural History, OH (CLEV)location not on record
3
NMBU:MINAlocation not on record
2
Hiwa Museum of Natural Historylocation not on record
2
Stockholm, SE
2
Laboratory of Systematic Entomology, The Hokkaido University Museum, Hokkaido University, Sapporo, Japanlocation not on record
1
Landesmuseum Kärntenlocation not on record
1
SBPlocation not on record
1
Research Collection of Wolfgang Starklocation not on record
1
Natural History Museum, Londonlocation not on record
1
New Haven, US
1
Uniwersytet Jagiellońskilocation not on record
1
CBDClocation not on record
1
68 institutions · 7 954 of 8 962 vouchered records shown · 1 008 without an institution code
09Environmental DNA68 detections
Where the DNA of Angerona prunaria 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 found68
Studies independent surveys2
Countries13
Verifiable raw sequence linked1
Signal confidence: moderateweighed across independent studies, places & mapped detections
Where its DNA was found
0 of 68 detections have coordinates
Open the map13 countries0
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 median15.8 °C 12.7–19.7
Seasonal swing summer↔winter19.1 °C
Max temp (day)19.7 °C 16.1–23.2
Min temp (night)11.5 °C 6.20–14.6
Precipitation78.8 mm/mo 56.3–216
Air humidity59.8 % 56.9–65.8
Moisture balance-33.7 mm/mo -78.3–100
Vapour deficit746 Pa 527–928
Wind speed3.00 m/s 1.60–4.80
Cloud cover38.1 % 34.4–47.6
CHELSA 1981–2010, ~9 km grid, at location & month of 53 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.