You can sponsor this page

Diaphus balanovi Prokofiev, Emelyanova, Orlov & Orlova, 2022

Upload your photos and videos
Google image
Image of Diaphus balanovi
No image available for this species;
drawing shows typical species in Myctophidae.

Classification / Names Κοινά ονόματα | Συνώνυμα | Catalog of Fishes(Γένος, Είδη) | ITIS | CoL | WoRMS | Cloffa

> Myctophiformes (Lanternfishes) > Myctophidae (Lanternfishes) > Diaphinae
Etymology: Diaphus: Greek, dis, dia = through + Greek, physa, phyo = to beget, to have as offspring (Ref. 45335)balanovi: Named for Dr. Andrei A. Balanov, A.V. Zhirmunsky National Scientific Center of Marine Biology, Far Eastern Branch of the Russian Academy of Sciences, Vladivostok.

Environment: milieu / climate zone / depth range / distribution range Οικολογία

Θαλασσινό(ά) βαθυπελαγικό(ς); εύρος βάθους 642 - 1030 m (Ref. 125672). Deep-water

Κατανομή Χώρες | Περιοχές FAO | Οικοσυστήματα | Παρουσίες | Point map | Εισαγωγές | Faunafri

Northwest Pacific: Emperor Seamount Chain

Μέγεθος / Βάρος / Age

Maturity: Lm ?  range ? - ? cm
Max length : 9.6 cm SL αρσενικό/απροσδιόριστο; (Ref. 125672)

Short description Κλείδες προσδιορισμού | Μορφολογία | Μορφομετρία

Μαλακές ραχιαίες ακτίνες (συνολικά) : 12 - 14; Μαλακές εδρικές ακτίνες: 12 - 14. This species is distinguished from most of the Diaphus fulgens species complex members, except D. rafinesquii (North Atlantic and the Mediterranean Sea) and D. kuroshio (Kuroshio Zone in the North Pacific), by having a higher gill-raker count 24-28, almost always 25 or more (vs. 14–20). Similar to D. kuroshio in the disposition of photophores (VO5, SAO1, and SAO2 on the same line, AOa1 below level of SAO2, Prc4 its own diameter below lateral line), but differs to the latter by the large luminous scale at PLO, large Dn, somewhat higher position of SAO3, otolith shape, and larger absolute size (at least 98 mm SL vs. about 70 mm). Otolith of Diaphus balanovi distinguished from the other species united in the Diaphus theta otolith group of Schwarzhans by the following characters: compressed shape with very weakly and uniformly convex outer face, rather steep and irregular predorsal rim, pronounced postdorsal angle, moderately long rostrum (18–19% of otolith length), and with 7-8 (usually eight) denticles along the ventral rim (Ref. 125672).

Βιολογία     Γλωσσάρι (π.χ. epibenthic)

All specimens were collected by bottom trawls with non-closing openings and was quite abundant in catches, contrary to the single specimens of the mesopelagic D. kuroshio and D. metopoclampus in the same hauls, indicating that the new species can be associated with the seamounts and may have a benthopelagic mode of life. The larger absolute size in comparison with its closest relative and possible ancestor (D. kuroshio) supports this assumption (Ref. 125672).

Life cycle and mating behavior Γεννητική Ωρίμανση | Αναπαραγωγή | Γεννοβολία | Αβγά | Γονιμότητα | Προνύμφες

Main reference Upload your references | Αναφορές | Συντονιστής : Paxton, John | Συνεργάτες

Prokofiev, A.M., O.R. Emelyanova, A.M. Orlov and S.Y. Orlova, 2022. A new species of Diaphus associated with seamounts of the Emperor Chain, North-Western Pacific Ocean (Teleostei: Myctophiformes: Myctophidae). J. Mar. Sci. Eng. 10(65):1-13. (Ref. 125672)

IUCN Red List Status (Ref. 130435: Version 2024-2)


CITES

Not Evaluated

CMS (Ref. 116361)

Not Evaluated

Threat to humans

  Harmless





Human uses

αλιεία: με δυνητικό ενδιαφέρον
FAO - Publication: search | FishSource |

Περισσότερες πληροφορίες

Trophic ecology
Τροφικά αντικείμενα
Σύσταση δίαιτας
Κατανάλωση τροφής
Food rations
Θηρευτές
Ecology
Οικολογία
Population dynamics
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
Distribution
Χώρες
Περιοχές FAO
Οικοσυστήματα
Παρουσίες
Εισαγωγές
BRUVS - Videos
Anatomy
Επιφάνεια βραγχίων
Brain
Otolith
Physiology
Body composition
Nutrients
Κατανάλωση οξυγόνου
Κολυμβητικός τύπος
Ταχύτητα κολύμβησης
Visual pigments
Fish sound
Diseases & Parasites
Toxicity (LC50s)
Genetics
Γενετική
Heterozygosity
Κληρονομικότητα
Human related
Aquaculture systems
Προφίλ υδατοκαλλιεργειών
Στελέχοι
Ciguatera cases
Stamps, coins, misc.
Taxonomy
Κοινά ονόματα
Συνώνυμα
Μορφολογία
Μορφομετρία
Φωτογραφίες
References
Αναφορές

Εργαλεία

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 = No PD50 data   [Uniqueness, from 0.5 = low to 2.0 = high].
Bayesian length-weight: a=0.01122 (0.00358 - 0.03515), b=2.99 (2.74 - 3.24), in cm total length, based on LWR estimates for this (Sub)family-body shape (Ref. 93245).
Τροφικό Επίπεδο (Ref. 69278):  3.1   ±0.3 se; based on size and trophs of closest relatives
Ελαστικότητα (Ref. 120179):  Υψηλό, ελάχιστος χρόνος για διπλασιασμό πληθυσμού < 15 μήνες (Preliminary K or Fecundity.).
Fishing Vulnerability (Ref. 59153):  Low vulnerability (10 of 100).