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 Common names | Synonyms | Catalog of Fishes(genus, species) | ITIS | CoL | WoRMS | Cloffa

Teleostei (teleosts) > 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 Ecology

Marine; bathypelagic; depth range 642 - 1030 m (Ref. 125672). Deep-water

Distribution Countries | FAO areas | Ecosystems | Occurrences | Point map | Introductions | Faunafri

Northwest Pacific: Emperor Seamount Chain

Size / Weight / Age

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

Short description Identification keys | Morphology | Morphometrics

Dorsal soft rays (total): 12 - 14; Anal soft rays: 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).

Biology     Glossary (e.g. 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 Maturities | Reproduction | Spawnings | Egg(s) | Fecundities | Larvae

Main reference Upload your references | References | Coordinator : Paxton, John | Collaborators

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)


CITES

Not Evaluated

CMS (Ref. 116361)

Not Evaluated

Threat to humans

  Harmless





Human uses

FAO - Publication: search | FishSource |

More information

Trophic ecology
Food items
Diet compositions
Food consumptions
Food rations
Predators
Ecology
Ecology
Population dynamics
Growths
Max. ages / sizes
Length-weight rel.
Length-length rel.
Length-frequencies
Mass conversions
Recruitments
Abundances
Life cycle
Reproduction
Maturities
Fecundities
Spawnings
Spawning aggregations
Egg(s)
Egg developments
Larvae
Larval dynamics
Distribution
Countries
FAO areas
Ecosystems
Occurrences
Introductions
BRUVS - Videos
Anatomy
Gill areas
Brains
Otoliths
Physiology
Body compositions
Nutrients
Oxygen consumptions
Swimming type
Swimming speeds
Visual pigment(s)
Fish sounds
Diseases / Parasites
Toxicities (LC50s)
Genetics
Genetics
Electrophoreses
Heritabilities
Human related
Aquaculture systems
Aquaculture profiles
Strains
Ciguatera cases
Stamps, coins, misc.
Outreach
Collaborators
Taxonomy
Common names
Synonyms
Morphology
Morphometrics
Pictures
References
References

Tools

Special reports

Download XML

Internet sources

AFORO (otoliths) | Aquatic Commons | BHL | Cloffa | BOLDSystems | Websites from users | Check FishWatcher | CISTI | Catalog of Fishes: genus, species | 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 | Tree of Life | Wikipedia: Go, Search | 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=0.01148 (0.00367 - 0.03596), b=2.99 (2.74 - 3.24), in cm total length, based on LWR estimates for this (Sub)family-body shape (Ref. 93245).
Trophic level (Ref. 69278):  3.1   ±0.3 se; based on size and trophs of closest relatives
Resilience (Ref. 120179):  High, minimum population doubling time less than 15 months (Preliminary K or Fecundity.).
Fishing Vulnerability (Ref. 59153):  Low vulnerability (10 of 100).