Magicicada tredecassini is a species of periodical cicada endemic to the United States. It has a 13-year lifecycle but is otherwise indistinguishable from the 17-year periodical cicada Magicicada cassini. The two species are usually discussed together as "cassini periodical cicadas" or "cassini-type periodical cicadas." Unlike other periodical cicadas, cassini-type males may synchronize their courting behavior so that tens of thousands of males sing and fly in unison.
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 Magicicada tredecassini has left across the world's sequence archives.
At a glance
DNA specimens29
BINs1
Marker genes1
eDNA detections17
Countries1
The DNA barcodethe species' typical barcode, built from every sequenced specimen
COI-5P1 000 bp consensus29 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. 100% of positions are identical in every specimen.
Where individuals differ — all 2 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)0.10%
Haplotypes9
BIN1
Most divergent pair0.40%
N.America
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
Organelle genome
Besides the big genome in the nucleus, cells carry a small, circular loop of DNA inside the cell's energy factories — the mitochondria. It is inherited almost only from the mother and is a leftover from ancient bacteria that moved into the cell. The mitochondrial markers above (ND*, COX, CYTB…) are read from exactly this loop. Outer ring = one strand, inner ring = the other.
▸ Tap any coloured segment — or a gene chip — to see what it is
Pick a coloured segment on the ring — or a gene chip — to read what that gene does.
protein-codingrRNAtRNA
07Deep time~0.32 Ma lineage
How far back this lineage goes — and how we know. Everything here is measured in Ma, short for “mega-annum”: millions of years ago. The chart reads left to right like a calendar of the Earth, from the deep past on the left to today at the right edgetop to bottom like a core drilled through the Earth, from the deep past at the top down to today at the bottom.
At a glance
DNA clock origin0.32 Ma TimeTree
When this lineage existed
How to read this: the coloured strip along the bottomdown the left is the geological calendar — the standard epochs (Pliocene, Pleistocene…) every museum uses, shown so you can see which chapter of Earth's history this lineage lived in. This lineage is a young one, so the strip is zoomed in to epochs — the finer subdivisions inside a period. The orange marker is the DNA clock: DNA accumulates mutations at a roughly steady rate, so comparing this species' DNA with its relatives estimates when the lineage split off — independently of any fossil.
DNA clock origin
08Occurrence & distribution
Record type1 834 records
Wild obs. + sensor1 625
Museum / vouchered209
Range
Area of Occupancy AOO2 776 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 accuracy83% within 1 km
≤100 m 937≤1 km 251≤10 km 25>10 km 213
1 426 georeferenced · 199 without coordinates
Open the mapobservation + sensor1 625
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 accuracy62% within 1 km
≤1 km 102≤10 km 50>10 km 13
165 georeferenced · 44 without coordinates
Open the institutions mapphysical evidence209
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 9 geolocated
Institutions and collections holding physical, vouchered specimens of this species — click a row to fly to it on the map.
Institution
Specimens
Colorado State Universitylocation not on record
99
Champaign, US
43
Mississippi State, US
28
Provo, US
13
Wuzhou, CN
11
University of Central Floridalocation not on record
3
Natural History Museum of Utahlocation not on record
2
East Lansing, US
2
Montgomery, US
1
9 institutions · 202 of 209 vouchered records shown · 4 without an institution code
09Environmental DNA17 detections
Where the DNA of Magicicada tredecassini 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 found17
Studies independent surveys1
Countries1
Signal confidence: weakweighed across independent studies, places & mapped detections
Where its DNA was found
0 of 17 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 median0.1 °C 0.1–0.1
Seasonal swing summer↔winter24.7 °C
Max temp (day)4.60 °C
Min temp (night)-3.50 °C
Precipitation77.7 mm/mo
Air humidity58.4 %
Moisture balance40.9 mm/mo
Vapour deficit258 Pa
Wind speed4.50 m/s
Cloud cover59.3 %
CHELSA 1981–2010, ~9 km grid, at location & month of 3 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.