Ampithoe ramondi is een vlokreeftensoort uit de familie van de Ampithoidae. De wetenschappelijke naam van de soort is voor het eerst geldig gepubliceerd in 1826 door Audouin.
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 Ampithoe ramondi has left across the world's sequence archives.
At a glance
DNA specimens28
BINs5
Marker genes2
eDNA detections24
Countries7
The DNA barcodethe species' typical barcode, built from every sequenced specimen
COI-5P658 bp consensus25 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. 75% of positions are identical in every specimen.
Where individuals differ — all 165 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)10.4%
Haplotypes8
BINs5
Most divergent pair15.2%
AsiaEurope
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
07Deep time~83.2 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 origin83.2 Ma TimeTree
When this lineage existed
How to read this: the coloured strip along the bottomdown the left is the geological calendar — the standard periods (Jurassic, Cretaceous…) every museum uses, shown so you can see which chapter of Earth's history this lineage lived in. The dashed rules marked ✦ are the five great mass extinctions. 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 originmass extinction
08Occurrence & distribution
Record type2 686 records
Wild obs. + sensor388
Museum / vouchered2 051
Other247
Origin
Native11
Range
Area of Occupancy AOO2 556 km²
Depth
0–200 m sunlit189
200–1000 m twilight0
1–4 km midnight0
>4 km abyssal0
median 4 m · max 100 m · 189 records with depth
Wildobservation + sensor
Human sightings and records, or camera-trap / sensor detections — someone (or a device) saw or captured the species in the wild.
Coordinate accuracy93% within 1 km
≤100 m 34≤1 km 42≤10 km 3>10 km 3
82 georeferenced · 306 without coordinates
Open the mapobservation + sensor388
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 accuracy69% within 1 km
≤100 m 117≤1 km 90≤10 km 57>10 km 36
300 georeferenced · 1 751 without coordinates
Open the institutions mapphysical evidence2 051
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 institutions11 of 35 geolocated
Institutions and collections holding physical, vouchered specimens of this species — click a row to fly to it on the map.
Institution
Specimens
Universidad Simón Bolívarlocation not on record
242
National Marine Biodiversity Institute of Korealocation not on record
218
DASSHlocation not on record
76
Sydney, AU
76
Brussels, BE
56
Washington, US
55
UNICAMPlocation not on record
50
Museu Nacional/Universidade Federal do Rio de Janeirolocation not on record
50
AUTHlocation not on record
46
Honolulu, US
44
RBINS-Scientific Heritagelocation not on record
30
Mexico City, MX
22
Unidad Multidisciplinaria de Docencia e Investigación, Campus Sisal, Facultad de Ciencias, Universidad Nacional Autónoma de Méxicolocation not on record
22
Los Angeles, US
15
FCMMlocation not on record
15
CEFASlocation not on record
14
Paris, FR
11
Universidad del Valle (UniValle)location not on record
8
Tromsø, NO
7
HCMR - IMBBClocation not on record
5
Institut Francais pour l'Etude de la Merlocation not on record
5
University of Aveiro, Centre for Environmental and Marine Studieslocation not on record
4
PNHSlocation not on record
4
486location not on record
3
Hellenic Centre of Marine Research; Institute for Oceanographylocation not on record
3
Bonn, DE
3
South Kensington, GB
2
Museo civico La Terra e l'Uomo di Crocetta del Montellolocation not on record
2
HCMR-IMBBClocation not on record
2
Florida Atlantic University, Harbor Branch Oceanographic Museumlocation not on record
1
Cantablocation not on record
1
Museum für Naturkunde Berlin (Zoological Collections)location not on record
1
Natick, US
1
University of Lodz, Dept of Invertebrate Zoology and Hydrobiologylocation not on record
1
Instituto de Investigaciones Marinas y Costeras José Benito Vives de Andreis - Invemarlocation not on record
1
35 institutions · 1 096 of 2 051 vouchered records shown · 34 without an institution code
09Environmental DNA24 detections
Where the DNA of Ampithoe ramondi 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 found24
Studies independent surveys1
Countries5
Signal confidence: weakweighed across independent studies, places & mapped detections
Where its DNA was found
0 of 24 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 median25.6 °C 15.2–25.7
Seasonal swing summer↔winter15.6 °C
Max temp (day)28.4 °C 18.2–29.6
Min temp (night)21.1 °C 12.6–22.2
Precipitation25.8 mm/mo 23.4–156
Air humidity55.7 % 54.4–61.1
Moisture balance-155 mm/mo
Vapour deficit1,451 Pa 712–1,508
Wind speed2.60 m/s
Cloud cover28.0 % 27.9–41.2
CHELSA 1981–2010, ~9 km grid, at location & month of 21 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.