The great spreadwing (Archilestes grandis) is a damselfly in the family Lestidae. When great spreadwings are startled they often return to the same perch or a perch nearby.
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 Archilestes grandis has left across the world's sequence archives.
At a glance
DNA specimens13
BINs2
Marker genes2
eDNA detections13
Countries3
The DNA barcodethe species' typical barcode, built from every sequenced specimen
COI-5P654 bp consensus8 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. 95% of positions are identical in every specimen.
Where individuals differ — all 35 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)1.6%
Haplotypes4
BINs2
Most divergent pair4.7%
N.America
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-5P18S-5P
animal barcoderibosomal
06Genome at a glanceGoaT · NCBI
The complete instruction manualArchilestes grandis 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≈938 336 822 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 Archilestes grandis0.94 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 levelChromosome
08Occurrence & distribution
Record type9 481 records
Wild obs. + sensor7 505
Museum / vouchered1 976
Origin
Native3
Range
Area of Occupancy AOO13 832 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 accuracy89% within 1 km
≤100 m 3 404≤1 km 1 265≤10 km 269>10 km 324
5 262 georeferenced · 2 243 without coordinates
Open the mapobservation + sensor7 505
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 accuracy73% within 1 km
≤100 m 705≤1 km 116≤10 km 254>10 km 55
1 130 georeferenced · 846 without coordinates
Open the institutions mapphysical evidence1 976
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 institutions24 of 42 geolocated
Institutions and collections holding physical, vouchered specimens of this species — click a row to fly to it on the map.
Institution
Specimens
Mexico City, MX
481
Washington, US
306
Odonata Centrallocation not on record
262
Ciudad de México, MX
116
University Park, US
69
Cornell University Insect Collectionlocation not on record
55
Durango, MX
36
Sam Noble Oklahoma Museum of Natural Historylocation not on record
35
Wuzhou, CN
32
New Haven, US
31
Champaign, US
29
Provo, US
25
Cleveland Museum of Natural History, OH (CLEV)location not on record
23
College Station, US
21
San Francisco, US
20
Essig Museum of Entomologylocation not on record
17
CASlocation not on record
17
National Biodiversity Institute, Costa Ricalocation not on record
17
OSUClocation not on record
15
Lubbock, US
13
East Lansing, US
8
Universidad de La Salle (La Salle)location not on record
7
Chicago, US
5
Montréal, CA
4
Juriquilla, MX
4
Denver, US
3
Los Angeles, US
3
Florida State Collection of Arthropods, The Museum of Entomologylocation not on record
3
Bonn, DE
3
Universidad del Magdalena (UniMagdalena)location not on record
3
US
3
US
2
Instituto Nacional de Biodiversidad, Costa Ricalocation not on record
2
Colorado State Universitylocation not on record
1
UCRClocation not on record
1
University of Guelphlocation not on record
1
University of Michigan, Museum of Zoologylocation not on record
1
San Luis Potosí, MX
1
Santa Barbara Museum of Natural Historylocation not on record
1
UCBMElocation not on record
1
Albuquerque, US
1
Awka, NG
1
42 institutions · 1 679 of 1 976 vouchered records shown · 297 without an institution code
09Environmental DNA13 detections
Where the DNA of Archilestes grandis 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 found13
Studies independent surveys1
Countries2
Signal confidence: weakweighed across independent studies, places & mapped detections
Where its DNA was found
0 of 13 detections have coordinates
Open the map2 countries0
pond or slough near River, restored wetland
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 median21.3 °C 15.5–23.4
Seasonal swing summer↔winter12.3 °C
Max temp (day)26.2 °C 20.9–31.2
Min temp (night)17.0 °C 11.8–18.9
Precipitation38.5 mm/mo 4.60–148
Air humidity58.4 % 52.0–61.8
Moisture balance-68.0 mm/mo -169–64.4
Vapour deficit1,055 Pa 743–1,337
Wind speed2.60 m/s 0.9–3.40
Cloud cover19.7 % 11.2–47.0
CHELSA 1981–2010, ~9 km grid, at location & month of 10 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.