Chrysomela saliceti

(Weise, 1884) · species

image placeholder — illustration coming later

Animalia/Arthropoda/Insecta/Coleoptera/Chrysomelidae/Chrysomela

At a glance

Occurrence records357

Data sources7

Biological traits0

DNA specimens16

eDNA detections14

Sources7 archives

Databases and archives Chrysomela saliceti's data was compiled from.

BioWikiNetmultilingual Wikipediamultilingual↗

GBIFGlobal Biodiversity Information Facility357 records↗

ENAEuropean Nucleotide Archive · EMBL-EBI14 eDNA detections↗

BOLD SystemsCentre for Biodiversity Genomics16 specimens↗

Open Tree of LifeOpenTreephylogeny backbone↗

GoaTGenomes on a Tree · Sangergenome & karyotype↗

NCBIUS National Library of Medicinegenome & karyotype↗

On this page5 sections

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

NarrativeWikipediaarticle

Occurrence & distributionGBIF357 records

Environmental DNA3 datasets · 5 countries14 detections

DNA & barcodingBOLD16 specimens

Genome at a glanceGoaT · NCBI≈739 Mbp

01Narrative

De kleine populierenhaan is een keversoort uit de familie bladkevers (Chrysomelidae). De wetenschappelijke naam van de soort werd in 1851 gepubliceerd door Suffrian.

No narrative description available for this taxon yet.

02Traits & measurements

No structured trait data for this taxon yet.

05DNA & barcoding16 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 Chrysomela saliceti has left across the world's sequence archives.

At a glance

DNA specimens16

BINs2

Marker genes1

eDNA detections14

Countries6

The DNA barcodethe species' typical barcode, built from every sequenced specimen

COI-5P658 bp consensus11 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. 82% of positions are identical in every specimen.

Where individuals differ — all 117 variable positions, in barcode order

3Cmostly conserved

4Tmostly conserved

7Amostly conserved

8Tmostly conserved

9Amostly conserved

10Cvariable

13Tvariable

14Amostly conserved

15Tmostly conserved

20Gmostly conserved

22Tvariable

23Tvariable

29Tvariable

36Tvariable

37Avariable

38Avariable

39Cvariable

43Avariable

46Avariable

50Tvariable

55Tvariable

59Tvariable

64Tvariable

67Gvariable

70Tvariable

79Avariable

82Tvariable

85Cvariable

88Gvariable

100Gvariable

121Gvariable

122Gvariable

127Tvariable

133Tvariable

142Cvariable

154Tvariable

163Avariable

169Tvariable

181Cvariable

184Gvariable

187Tvariable

190Avariable

202Avariable

217Avariable

220Avariable

232Cvariable

235Cvariable

238Tvariable

241Gvariable

242Cvariable

250Tvariable

268Cvariable

271Avariable

274Tmostly conserved

277Cvariable

278Tvariable

280Gvariable

283Cvariable

292Gvariable

319Avariable

328Gvariable

334Avariable

337Avariable

347Cvariable

349Avariable

353Gvariable

358Cvariable

361Tvariable

364Cvariable

370Tvariable

373Gvariable

374Gvariable

376Avariable

379Tvariable

382Avariable

385Tvariable

386Tvariable

388Avariable

400Gvariable

403Avariable

409Avariable

412Tvariable

421Tvariable

433Gvariable

439Avariable

451Avariable

460Cvariable

466Avariable

469Cvariable

472Cvariable

484Cvariable

487Cvariable

496Avariable

508Tvariable

523Tvariable

529Avariable

535Cvariable

536Cvariable

553Tvariable

557Tvariable

565Avariable

571Tvariable

574Tvariable

581Cvariable

589Cvariable

595Cvariable

596Tvariable

598Avariable

607Avariable

610Tvariable

616Tvariable

619Gvariable

625Avariable

628Tvariable

631Gvariable

637Tvariable

652Tvariable

AACTTTATACTTTATTTTTGGTTTTTGGTCAGGAATAACAGGAACATCTTTAAGTATTTTAATTCGGGCTGAATTAGGAAATCCCGGGAC …

Variant network

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)8.7%

Haplotypes5

BINs2

Most divergent pair16.6%

Europe

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.

Chrysomela populisame genus10.5%Chrysomela cupreasame genus12.3%Chrysomela collarissame genus15.2%Parasa darmasame order16.0%Phostria vitriferasame order16.7%

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

animal barcode

06Genome at a glanceGoaT · NCBI

The complete instruction manual Chrysomela saliceti 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≈738 629 865 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 Chrysomela saliceti0.74 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

Completeness99% BUSCO

08Occurrence & distribution

Record type357 records

Wild obs. + sensor254

Museum / vouchered102

Other1

Range

Area of Occupancy AOO976 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 accuracy52% within 1 km

≤100 m 59≤1 km 15≤10 km 69

143 georeferenced · 111 without coordinates

Open the mapobservation + sensor254

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 accuracy54% within 1 km

≤100 m 12≤1 km 32≤10 km 35>10 km 3

82 georeferenced · 20 without coordinates

Open the institutions mapphysical evidence102

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 institutions6 of 16 geolocated

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

Institution	Specimens
SLU Artdatabankenlocation not on record	25
Natural History Museum Rotterdamlocation not on record	15
Salzburg, AT	14
Helsinki, FI	6
Muzeum Górnośląskie w Bytomiulocation not on record	6
South Kensington, GB	5
Tilburg, NL	4
Tartu, EE	3
Natural History Museum, Londonlocation not on record	3
Winterthur, CH	3
Bavarian State Collection of Zoologylocation not on record	2
NHMOlocation not on record	2
ZMAAlocation not on record	2
Naturalis Biodiversity Centerlocation not on record	1
IFR-DNFlocation not on record	1
NTNU-VMlocation not on record	1

16 institutions · 93 of 102 vouchered records shown · 9 without an institution code

09Environmental DNA14 detections

Where the DNA of Chrysomela saliceti 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 found14

Studies independent surveys3

Countries5

Verifiable raw sequence linked3

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

Where its DNA was found

0 of 14 detections have coordinates

Open the map5 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 median15.3 °C 14.2–18.3

Seasonal swing summer↔winter18.5 °C

Max temp (day)19.4 °C 17.8–21.4

Min temp (night)10.6 °C 9.10–14.5

Precipitation80.5 mm/mo 60.9–134

Air humidity58.1 % 57.2–60.0

Moisture balance-39.2 mm/mo -49.5–41.2

Vapour deficit724 Pa 660–901

Wind speed2.70 m/s 1.90–3.80

Cloud cover41.0 % 36.1–43.5

CHELSA 1981–2010, ~9 km grid, at location & month of 12 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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