Nebria gyllenhali is een keversoort uit de familie van de loopkevers (Carabidae). De wetenschappelijke naam van de soort is voor het eerst geldig gepubliceerd in 1806 door Schonherr.
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 Nebria gyllenhali has left across the world's sequence archives.
At a glance
DNA specimens15
BINs4
Marker genes2
eDNA detections3
Countries3
The DNA barcodethe species' typical barcode, built from every sequenced specimen
COI-5P658 bp consensus6 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. 91% of positions are identical in every specimen.
Where individuals differ — all 61 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)3.7%
Haplotypes5
BINs3
Most divergent pair7.9%
N.AmericaEurope
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-5P
animal barcode
06Genome at a glanceGoaT
The complete instruction manualNebria gyllenhali 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.
Chromosomes & ploidyhow the DNA is packaged
2n is the full chromosome count in a normal body cell; n is a gamete (egg or sperm), which carries half. Ploidy is how many complete chromosome sets each cell holds — 2× (diploid) is typical for animals, while higher levels (polyploidy) are common in plants. Click any value below to see the underlying records and sources.
Ploidy records — measured levels and diploid/polyploid inferences · click for sources
diploid1×GoaT · Coleoptera Karyotype Database
GoaT · Coleoptera Karyotype Database
08Occurrence & distribution
Record type2 139 records
Wild obs. + sensor350
Museum / vouchered1 789
Origin
Native956
Range
Area of Occupancy AOO1 780 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 accuracy1% within 1 km
≤100 m 3≤10 km 347
350 georeferenced
Open the mapobservation + sensor350
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 accuracy2% within 1 km
≤100 m 3≤1 km 30≤10 km 1 678>10 km 17
1 728 georeferenced · 61 without coordinates
Open the institutions mapphysical evidence1 789
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 institutions8 of 23 geolocated
Institutions and collections holding physical, vouchered specimens of this species — click a row to fly to it on the map.
Institution
Specimens
Bern, CH
555
Geneva, CH
159
Naturmuseum Solothurnlocation not on record
107
Naturéum — Muséum cantonal des sciences naturelles, Lausanne, Département Zoologielocation not on record
70
Musee d'Histoire Naturallelocation not on record
42
Museum Ludovicae Ulricae, Zoology Institute of the University of Uppsalalocation not on record
33
Paro, BT
25
Royal Saskatchewan Museumlocation not on record
24
Provo, US
22
Frauenfeld, CH
19
Dhaka, BD
18
Espace pour la vielocation not on record
13
OSUClocation not on record
9
Chicago, US
6
Museo civico di Storia naturale Giacomo Doria di Genova | Giacomo Doria Natural History Museum in Genoalocation not on record
5
Muzeum i Instytut Zoologii Polskiej Akademii Nauklocation not on record
4
McGill Universitylocation not on record
3
FEBlocation not on record
3
Denver, US
2
WIlocation not on record
2
University of Alberta Museums (UAM)location not on record
2
McGill University, Lyman Entomological Museumlocation not on record
1
Colorado State Universitylocation not on record
1
23 institutions · 1 125 of 1 789 vouchered records shown · 664 without an institution code
09Environmental DNA3 detections
Where the DNA of Nebria gyllenhali 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 found3
Studies independent surveys1
Countries1
Signal confidence: weakweighed across independent studies, places & mapped detections
Where its DNA was found
0 of 3 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 median11.7 °C 11.7–11.7
Seasonal swing summer↔winter34.8 °C
Max temp (day)15.2 °C
Min temp (night)7.40 °C
Precipitation173 mm/mo
Air humidity61.9 %
Moisture balance67.0 mm/mo
Vapour deficit524 Pa
Wind speed5.60 m/s
Cloud cover55.2 %
CHELSA 1981–2010, ~9 km grid, at location & month of 1 detection point · 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.
