-
- About this page
- Languages
- User feedbacks
- Αναφορά
- Uploads
-
Related species
- Species in
Eptatretus - Species in
Myxinidae - - Classification -
- Eptatretinae
- Myxinidae
- Myxiniformes
- Myxini
- Chordata
- Animalia
- Species in
-
Eptatretus cryptus Roberts & Stewart, 2015
Cryptic hagfish
Add your observation in Fish Watcher
| Native range | All suitable habitat | Point map | Year 2050 |
|
| This map was computer-generated and has not yet been reviewed. |
| Eptatretus cryptus AquaMaps Data sources: GBIF OBIS |
Upload your photos and videos
Google image
No image available for this species;
drawing shows typical species in Myxinidae.
Google image
drawing shows typical species in Myxinidae.
Classification / Names Κοινά ονόματα | Συνώνυμα | Catalog of Fishes(Γένος, Είδη) | ITIS | CoL | WoRMS | Cloffa
Μυξίνοι (hagfishes) > Myxiniformes (Hagfishes) > Myxinidae (Hagfishes) > Eptatretinae
Etymology: Eptatretus: hepta (Gr.), seven; tretos (Gr.), perforated (i.e., with holes), referring to seven gill apertures on what would later be described as Homea banksii (=E. cirrhatus) [range within genus is 6-14 pairs of gill apertures] (See ETYFish); cryptus: From kryptos (Gr.), hidden or secret, referring to its similar morphology to E. cirrhatus, with which it has been confused in the past (See ETYFish).
Etymology: Eptatretus: hepta (Gr.), seven; tretos (Gr.), perforated (i.e., with holes), referring to seven gill apertures on what would later be described as Homea banksii (=E. cirrhatus) [range within genus is 6-14 pairs of gill apertures] (See ETYFish); cryptus: From kryptos (Gr.), hidden or secret, referring to its similar morphology to E. cirrhatus, with which it has been confused in the past (See ETYFish).
Environment: milieu / climate zone / depth range / distribution range Οικολογία
Θαλασσινό(ά) βαθύβιο(ς); εύρος βάθους 96 - 922 m (Ref. 115309). Deep-water
Κατανομή Χώρες | Περιοχές FAO | Οικοσυστήματα | Παρουσίες | Point map | Εισαγωγές | Faunafri
Western Pacific: New Zealand.
Μέγεθος / Βάρος / Age
Short description Κλείδες προσδιορισμού | Μορφολογία | Μορφομετρία
Ραχιαίες άκανθες (συνολικά) : 0; Μαλακές ραχιαίες ακτίνες (συνολικά) : 0; Εδρικές άκανθες: 0; Μαλακές εδρικές ακτίνες: 0. Diagnosis: characterized by the combination of the following characters: 7 pairs of gill pouches, 3/3 multicusps, 12–15 prebranchial slime pores (modally 14), 78–86 total slime pores, slime pores without narrow white rim, preocular length 4.8–5.8% TL, and body colour brown to dark brown; differs from all other congeners except E. caribbeaus, E. menezesi, E. strahani, E. cirrhatus, and E. goliath by having 7 pairs of gill pouches and 3/3 multicusps; Eptatretus caribbeaus, E. menezesi, and E. strahani are not found in New Zealand; differs from E. caribbeaus by the number of anterior unicusps (10–11 versus 11–13), posterior unicusps (8–10 versus 10–11), and body colour (brown to dark brown versus light tan); differs from E. menezesi by the tail slime pores (11–14 versus 14–18), total slime pores (78–86 versus 86–94), and ventral finfold colour (brown versus whitish margin); it differs from E. strahani by having visible (versus absent) eyespots, rounded (versus slit-like) 1st few branchial apertures, vestigial (versus welldeveloped) ventral finfold (0.17–0.64%TL versus 1.12–1.16%TL), rounded (versus angled) ventral caudal fin profile, and shallower tail depth (8.1–10.6%TL versus 10.9–12.7%TL); differentiation from E. cirrhatus by the prebranchial slime pores (12–15, modally 14 versus 15– 18, modally 16), its more robust appearance (body depth 8.9–12.0% TL versus 5.9–11.2% TL, often <8.6% TL), and body colour (brown to dark brown versus dark brown to purple-brown); some, and often most, slime pores of E. cirrhatus have a narrow white rim, whereas slime pores in E. cryptus sp. nov. are the same colour as the rest of the body; care must be taken not to interpret residual slime or internal structure of the slime pore for the presence of a white rim; Eptatretus cryptus differs from E. goliath by the trunk slime pores (46–54 versus 56–60) and total slime pores (78–86 versus 89–95); the following character can also help in dissociating E. cryptus from E. goliath: preocular length (>4.8 versus 3.7–5.2% TL) and prebranchial length (>20.3 versus 18.3–20.9% TL) (Ref. 115309).
This species is more commonly found deeper than 500 m. Its biology is largely unknown because it has been misidentified as the common hagfish E. cirrhatus; its stable carbon and nitrogen isotope signature indicated that this species feeds at a high trophic level, 3 levels above primary producers (Ref. 115309).
Life cycle and mating behavior Γεννητική Ωρίμανση | Αναπαραγωγή | Γεννοβολία | Αβγά | Γονιμότητα | Προνύμφες
Main reference
Upload your references | Αναφορές | Συντονιστής | Συνεργάτες
Zintzen, V., C.D. Roberts, L. Shepherd, A.L. Stewart, C.D. Struther, M.J. Anderson, M. McVeagh, M. Noren and B. Fernholm, 2015. Review and phylogeny of the New Zealand hagfishes (Myxiniformes: Myxinidae), with description of three new species. Zool. J. Linnean Soc. 174:363-393. (Ref. 115309)
CITES
Not Evaluated
Threat to humans
Harmless
Human uses
αλιεία: χωρίς ενδιαφέρον
FAO - Publication: search | FishSource |
Περισσότερες πληροφορίες
Trophic ecology
Τροφικά αντικείμενα
Σύσταση δίαιτας
Κατανάλωση τροφής
Food rations
Θηρευτές
Τροφικά αντικείμενα
Σύσταση δίαιτας
Κατανάλωση τροφής
Food rations
Θηρευτές
Population dynamics
Παράμετροι Αύξησης
Max. ages / sizes
Length-weight rel.
Length-length rel.
Length-frequencies
Mass conversion
Στρατολόγηση
Αφθονία
Παράμετροι Αύξησης
Max. ages / sizes
Length-weight rel.
Length-length rel.
Length-frequencies
Mass conversion
Στρατολόγηση
Αφθονία
Life cycle
Αναπαραγωγή
Γεννητική Ωρίμανση
Maturity/Gills rel.
Γονιμότητα
Γεννοβολία
Spawning aggregations
Αβγά
Egg development
Προνύμφες
Δυναμική προνυμφών
Αναπαραγωγή
Γεννητική Ωρίμανση
Maturity/Gills rel.
Γονιμότητα
Γεννοβολία
Spawning aggregations
Αβγά
Egg development
Προνύμφες
Δυναμική προνυμφών
Anatomy
Επιφάνεια βραγχίων
Brain
Otolith
Επιφάνεια βραγχίων
Brain
Otolith
Physiology
Body composition
Nutrients
Κατανάλωση οξυγόνου
Κολυμβητικός τύπος
Ταχύτητα κολύμβησης
Visual pigments
Fish sound
Diseases & Parasites
Toxicity (LC50s)
Body composition
Nutrients
Κατανάλωση οξυγόνου
Κολυμβητικός τύπος
Ταχύτητα κολύμβησης
Visual pigments
Fish sound
Diseases & Parasites
Toxicity (LC50s)
Genetics
Γενετική
Heterozygosity
Κληρονομικότητα
Γενετική
Heterozygosity
Κληρονομικότητα
Human related
Aquaculture systems
Προφίλ υδατοκαλλιεργειών
Στελέχοι
Ciguatera cases
Stamps, coins, misc.
Aquaculture systems
Προφίλ υδατοκαλλιεργειών
Στελέχοι
Ciguatera cases
Stamps, coins, misc.
Εργαλεία
E-book | Οδηγός πεδίου | Ανάλυση κατά μήκος συνθέσεων | Εργαλείο ιστορίας ζωής | Σημειακός χάρτης | Classification Tree
| Catch-MSY |
Special reports
Download XML
Διαδικτυακές πηγές
AFORO (otoliths) | Aquatic Commons | BHL | Cloffa | BOLDSystems | Websites from users | Check FishWatcher | CISTI | Catalog of Fishes: Γένος, Είδη | DiscoverLife | ECOTOX | FAO - Publication: search | Faunafri | Fishipedia | Fishtrace | GenBank: genome, nucleotide | GloBI | Google Books | Google Scholar | Google | IGFA World Record | MitoFish | Otolith Atlas of Taiwan Fishes | PubMed | Reef Life Survey | Socotra Atlas | Δέντρο Ζωής | Wikipedia: Go, αναζήτηση | World Records Freshwater Fishing | Zoobank | Zoological Record
Estimates based on models
Phylogenetic diversity index (Ref. 82804): PD50 = 0.5000 [Uniqueness, from 0.5 = low to 2.0 = high].
Bayesian length-weight: a=0.00204 (0.00094 - 0.00444), b=2.93 (2.74 - 3.12), in cm total length, based on LWR estimates for this (Sub)family-body shape (Ref. 93245).
Τροφικό Επίπεδο (Ref. 69278): 4.4 ±0.7 se; based on size and trophs of closest relatives
Ελαστικότητα (Ref. 120179): Χαμηλό, ελάχιστος χρόνος για διπλασιασμό πληθυσμού 4,5 - 14 έτη (Preliminary K or Fecundity.).
Fishing Vulnerability (Ref. 59153): High vulnerability (57 of 100).