Caranx ignobilis
(Forsskål, 1775) · speciesAt a glance
Sources12 archives
Databases and archives Caranx ignobilis's data was compiled from.
WikipediaWikimedia Foundation16 languages↗
BioWikiNetmultilingual Wikipediamultilingual↗
GBIFGlobal Biodiversity Information Facility11 583 records↗
OBISOcean Biodiversity Information System11 111 records↗
ENAEuropean Nucleotide Archive · EMBL-EBI328 eDNA detections↗
BOLD SystemsCentre for Biodiversity Genomics150 specimens↗
Open Tree of LifeOpenTreephylogeny backbone↗
GoaTGenomes on a Tree · Sangergenome & karyotype↗
NCBIUS National Library of Medicinegenome & karyotype↗
WikidataWikimedia Foundationstructured facts↗
Catalogue of LifeCOLtaxonomy↗
GLoBIGlobal Biotic Interactionsbiotic interactions↗Every layer below draws on the sources above — open one to explore it, or use ← → to move between tabs.
The giant trevally (Caranx ignobilis), also known as the lowly trevally, barrier trevally, giant kingfish or ulua, is a species of large marine fish classified in the jack family, Carangidae. The giant trevally is distributed throughout the tropical waters of the Indo-Pacific region, with a range stretching from South Africa in the west to Hawaii in the east, including Japan in the north and Australia in the south. Two were documented in the eastern tropical Pacific in the 2010s (one captured off Panama and another sighted at the Galápagos), but it remains to be seen if the species will become established there. The giant trevally is distinguished by its steep head profile, strong tail scutes, and a variety of other more detailed anatomical features. It is normally a silvery colour with occasional dark spots, but males may be black once they mature. It is the largest fish in the genus Caranx, growing to a maximum known size of 170 cm (67 in) and a weight of 80 kg (176 lbs). The giant trevally inhabits a wide range of marine environments, from estuaries, shallow bays and lagoons as a juvenile to deeper reefs, offshore atolls and large embayments as an adult. Juveniles of the species are known to live in waters of very low salinity such as coastal lakes and upper reaches of rivers, and tend to prefer turbid waters. The giant trevally is an apex predator in most of its habitats, and is known to hunt individually and in schools. The species predominantly takes various fish as prey, although crustaceans, cephalopods and molluscs make up a considerable part of their diets in some regions. The giant trevally employs novel hunting strategies, including shadowing monk seals to pick off escaping prey, as well as using sharks to ambush prey. Footage released in 2017 on Blue Planet II revealed a group of approximately 50 giant trevally hunting terns, specifically fledglings still learning to fly and which crash land in the water, as well as both fledglings and adults unfortunate enough to fly low enough for the fish to pounce on them, in Farquhar Atoll in the Seychelles. The giant trevally reproduces in the warmer months, with peaks differing by region. Spawning occurs at specific stages of the lunar cycle, when large schools congregate to spawn over reefs and bays, with reproductive behaviour observed in the wild. The fish grows relatively fast, reaching sexual maturity at a length of around 60 cm at three years of age. The giant trevally is both an important species to commercial fisheries and a recognised gamefish, with the species taken by nets and lines by professionals and by bait and lures by anglers. Catch statistics in the Asian region show hauls of 4,000–10,000 tonnes, while around 10,000 lbs of the species is taken in Hawaii each year. The species is considered poor to excellent table fare by different authors, although ciguatera poisoning is common from eating the fish. Dwindling numbers around the main Hawaiian Islands have also led to several proposals to reduce the catch of fish in this region.
No narrative description available for this taxon yet.
Size & morphology2
Habitat & environment3
Uses & economy1
Other traits3
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 Caranx ignobilis 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 Caranx ignobilis 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).
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 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.
Record type22 694 records
Origin
Range
Depth
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 48 geolocated
Institutions and collections holding physical, vouchered specimens of this species — click a row to fly to it on the map.
| Institution | Specimens |
|---|---|
| Kagoshima University Museumlocation not on record | 160 |
| Sydney, AU | 132 |
| Paris, FR | 115 |
| New Haven, US | 104 |
| CASlocation not on record | 87 |
| Australian National Fish Collectionlocation not on record | 66 |
| Museum and Art Gallery of the Northern Territorylocation not on record | 42 |
| South African Institute for Aquatic Biodiversitylocation not on record | 35 |
| Washington, US | 35 |
| Curtin Universitylocation not on record | 34 |
| Natick, US | 23 |
| Chicago, US | 12 |
| CSIRO Oceans and Atmospherelocation not on record | 12 |
| 10 | |
| Western Australian Museumlocation not on record | 8 |
| DEWlocation not on record | 6 |
| Mutare Museumlocation not on record | 6 |
| Cambridge, US | 5 |
| UWFClocation not on record | 4 |
| Museums Victorialocation not on record | 4 |
| Vancouver, CA | 4 |
| FishBaselocation not on record | 3 |
| DOI/NPS, Salem Maritime National Historic Sitelocation not on record | 3 |
| Fisheries Research Laboratory, Mie Universitylocation not on record | 3 |
| University of California San Diegolocation not on record | 3 |
| Toronto, CA | 2 |
| SEAOBISlocation not on record | 2 |
| Los Angeles, US | 2 |
| Wuzhou, CN | 2 |
| Museo civico La Terra e l'Uomo di Crocetta del Montellolocation not on record | 2 |
| Instituto de Investigaciones Marinas y Costeras José Benito Vives de Andréis (INVEMAR)location not on record | 2 |
| Honolulu, US | 2 |
| MNHAHlocation not on record | 1 |
| South Kensington, GB | 1 |
| Florida Museum of Natural History- Zoology, Paleontology & Paleobotanylocation not on record | 1 |
| Stockholm, SE | 1 |
| Muséum National d'Histoire Naturellelocation not on record | 1 |
| Ann Arbor, US | 1 |
| National Marine Biodiversity Institute of Korealocation not on record | 1 |
| North Carolina Museum of Natural Scienceslocation not on record | 1 |
| Yokosuka City Museumlocation not on record | 1 |
| Puerto Ayora, EC | 1 |
| Food Research Institute, Ministry of Agriculture, Forestry and Fisherieslocation not on record | 1 |
| Academia Sinica, Biodiversity Research Centerlocation not on record | 1 |
| Helsinki, FI | 1 |
| Oregon State Universitylocation not on record | 1 |
| No Voucherlocation not on record | 1 |
| Institut Halieutique et des Sciences Marineslocation not on record | 1 |
Where the DNA of Caranx ignobilis 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.