Amia calva
Linnaeus, 1766 · speciesAt a glance
Sources12 archives
Databases and archives Amia calva's data was compiled from.
WikipediaWikimedia Foundation17 languages↗
Animal Diversity WebUniv. of Michigan MZspecies account↗
BioWikiNetmultilingual Wikipediamultilingual↗
GBIFGlobal Biodiversity Information Facility10 856 records↗
ENAEuropean Nucleotide Archive · EMBL-EBI265 eDNA detections↗
BOLD SystemsCentre for Biodiversity Genomics28 specimens↗
Open Tree of LifeOpenTreephylogeny backbone↗
GoaTGenomes on a Tree · Sangergenome & karyotype↗
NCBIUS National Library of Medicinegenome & karyotype↗
Paleobiology DatabasePBDB consortiumfossil record↗
WikidataWikimedia Foundationstructured facts↗
Catalogue of LifeCOLtaxonomy↗Every layer below draws on the sources above — open one to explore it, or use ← → to move between tabs.
The bowfin (Amia calva) is a bony fish, native to North America. Common names include mudfish, mud pike, dogfish, grindle, grinnel, swamp trout, and choupique. It is regarded as a relict, being the sole surviving species of the Halecomorphi, a group of fish that first appeared during the Early Triassic, around 250 million years ago. The bowfin is often considered a "primitive fish" because they have retained some morphological characteristics of their early ancestors. The closest living relatives of bowfins are gars, with the two groups being united in the clade Holostei. Bowfins are demersal freshwater piscivores, commonly found throughout much of the eastern United States, and in southern Ontario and Quebec. Fossil deposits indicate Amiiformes were once widespread in both freshwater and marine environments across North and South America, Europe, Asia, and Africa. Now, their range is limited to much of the eastern United States and adjacent southern Canada, including the drainage basins of the Mississippi River, Great Lakes, and various rivers exiting in the Eastern Seaboard or Gulf of Mexico. Their preferred habitat includes vegetated sloughs, lowland rivers and lakes, swamps, and backwater areas; they are also occasionally found in brackish water. They are stalking, ambush predators known to move into the shallows at night to prey on fish and aquatic invertebrates such as crawfish, mollusks, and aquatic insects. Like gars, bowfin are bimodal breathers – they have the capacity to breathe both water and air. Their gills exchange gases in the water allowing them to breathe, but they also have a gas bladder that serves to maintain buoyancy, and also allows them to breathe air by means of a small pneumatic duct connected from the foregut to the gas bladder. They can break the surface to gulp air, which allows them to survive conditions of aquatic hypoxia that would be lethal to most other species.
No narrative description available for this taxon yet.
Size & morphology2
Life cycle & reproduction3
Habitat & environment2
Uses & economy1
Other traits1
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 Amia calva has left across the world's sequence archives.
At a glance
★ 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.
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.
The complete instruction manual Amia calva 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
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).
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.
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.
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
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 solid bar is the fossil range: the span between the oldest and the youngest fossil that palaeontologists have assigned to Amia calva. Above itBeside it, each dot is one dated fossil find — few enough to count, so they are drawn individually rather than as a graph. 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. Where the DNA reaches further back than the oldest fossil, the gap is hatched: the ghost lineage. It means the lineage was already out there, but has left us nothing we have dug up yet.
How it livedPBDB
Record type10 868 records
Origin
Range
Wildobservation + sensor
Human sightings and records, or camera-trap / sensor detections — someone (or a device) saw or captured the species in the wild.
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.
Wildobservation + sensor
Human sightings and records, or camera-trap / sensor detections — someone (or a device) saw or captured the species in the wild.
Holding institutions18 of 41 geolocated
Institutions and collections holding physical, vouchered specimens of this species — click a row to fly to it on the map.
| Institution | Specimens |
|---|---|
| Florida Museum of Natural History- Zoology, Paleontology & Paleobotanylocation not on record | 169 |
| Champaign, US | 149 |
| North Carolina Museum of Natural Scienceslocation not on record | 132 |
| University of Texas Biodiversity Collections (UTBC)location not on record | 123 |
| New Haven, US | 95 |
| Ann Arbor, US | 94 |
| Ohio State University - Fish Division, Columbus, OH (OSUM)location not on record | 86 |
| University of Alabamalocation not on record | 82 |
| Chicago, US | 78 |
| University of Minnesota, James Ford Bell Museum of Natural Historylocation not on record | 74 |
| Toronto, CA | 62 |
| Texas Memorial Museum, Texas Natural History Collectionlocation not on record | 43 |
| Washington, US | 40 |
| Montgomery, US | 33 |
| Cambridge, US | 32 |
| Museo civico La Terra e l'Uomo di Crocetta del Montellolocation not on record | 32 |
| Southeastern Louisiana University, Vertebrate Museumlocation not on record | 25 |
| Louisiana State University, Museum of Zoologylocation not on record | 19 |
| Sam Noble Oklahoma Museum of Natural Historylocation not on record | 11 |
| Los Angeles, US | 11 |
| Texas Cooperative Wildlife Collectionlocation not on record | 11 |
| Central Michigan University Museum of Cultural and Natural Historylocation not on record | 8 |
| CASlocation not on record | 7 |
| Vancouver, CA | 6 |
| University of California San Diegolocation not on record | 5 |
| Museu de Zoologia da Universidade de Sao Paulolocation not on record | 5 |
| Stockholm, SE | 3 |
| 3 | |
| APSUlocation not on record | 3 |
| ASUlocation not on record | 3 |
| Frankfurt am Main | 3 |
| Oregon State Universitylocation not on record | 3 |
| University of Alberta Museumslocation not on record | 2 |
| Wuzhou, CN | 2 |
| Sydney, AU | 2 |
| South Kensington, GB | 2 |
| South African Institute for Aquatic Biodiversitylocation not on record | 2 |
| Muzeum i Instytut Zoologii Polskiej Akademii Nauklocation not on record | 1 |
| University of Kansas, Biodiversity Research Centerlocation not on record | 1 |
| Chicago, US | 1 |
| Paris, FR | 1 |
Where the DNA of Amia calva 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
Where its DNA was found
How strong is each trace?
Modelled climatemodelled
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.