dcsimg

Data on Catalog of Fishes

provided by Deep sea Fishes of the World LifeDesk

View data on Catolog of Fishes here.

license
cc-by-nc
copyright
Kenaley, Christopher
author
Kenaley, Christopher

Description

provided by Deep sea Fishes of the World LifeDesk

Barbel length is 13%–30% SL in specimens smaller than 65 mm, 15%–28% in those 65–90 mm, and 23%–33% in those larger than 90 mm. Apparently the increase in relative length occurs at different rates in small specimens, but no further change with growth occurs after about 90 mm SL.

The axis of the stem varies from lightly to darkly peppered with melanophores, or streaked with dark pigment, the variation apparently not size related. The chevron-shaped or roundish striated areas on the stem are unpigmented. The axis between the bulbs is darkly peppered or streaked, especially distad where it extends onto the proximal quarter to third of the distal bulb as a black cap. The filament axis is without melanophores or with a few proximally.

Proximal and distal bulbs vary in shape from spheroidal to ovoid. The proximal bulb is 0.1%– 0.7% SL, distal bulb 0.4%–l.l% SL and 1–5 times proximal–bulb length, neither bulb changing size relative to SL with growth. Several specimens have non–opaque distal bulbs with a reticulate or dendritic network internally. The distance between bulbs is 0.5%–1.5% SL in small specimens, decreasing in relative length to 0.1 %–0.6% in the largest. The distance is 0.3–2.5 times as long as the distal bulb, with no relation to size of fish.

The terminal filament is short, 0.3%–2.5% SL, 0.4–4.0 times distal–bulb length, apparently not changing with growth. It bifurcates or trifurcates near its base, and occasionally branches again further distad. There are no bulblets in the filament.

The postorbital organs of 12 large males (125– 152 mm SL) are 1.4%–2.1% SL, 56%–82% fleshy orbit length. A 134 mm male has a postorbital organ only 1.0% SL, 45% fleshy orbit length, and one 105 mm has an organ 1.2% SL, 43% fleshy orbit length. In one female the organ is 0.9%; in all others it is 0.8% or less.

There are eight paired dorsal spots between occiput and dorsal–fin origin, one beneath the dorsal fin, and one variably present on the caudal peduncle.

In two freshly caught specimens the proximal bulb was yellow, the distal bulb blue.

license
cc-by-nc
copyright
Kenaley, Christopher
author
Kenaley, Christopher

Diagnostic Description

provided by Deep sea Fishes of the World LifeDesk

Two terminal bulbs separated by a short interspace, 0.1%–1.5% SL, about 0.3– 2.5 times distal–bulb length. Proximal bulb small, 0.1%–0.7% SL. Distal bulb 0.4%–1.1% SL, 1–5 times proximal–bulb length, with distinctive black pigment cap on proximal end. Terminal filament short, 0.3%–2.5% SL, without prominent bulblets. Barbel length 13%–33% SL. Stem axis lightly to darkly pigmented. External chevron-shaped or roundish striated areas on stem unpigmented. Paired dorsal spots between occiput and dorsal-fin origin 8..

license
cc-by-nc
copyright
Kenaley, Christopher
author
Kenaley, Christopher

Distribution

provided by Deep sea Fishes of the World LifeDesk

Eastern Gulf of Mexico, Caribbean Sea, and from 29°N, 80°W (off northern Florida) through the Bahamas, Antilles, and offshore roughly parallel to the coast of South America to about 23°S, extending east to about 30 °W off central Brazil.

license
cc-by-nc
copyright
Kenaley, Christopher
author
Kenaley, Christopher

Main Reference

provided by Deep sea Fishes of the World LifeDesk

Gomon JR, Gibbs RH, Jr. 1985. Taxonomy and distribution of the stomioid fish genus Eustomias (Melanostomiidae), II: Biradiostomias, new subgenus. Smithsonian Contributions to Zoology No. 409:1–58.

license
cc-by-nc
copyright
Kenaley, Christopher
author
Kenaley, Christopher

Morphology

provided by Deep sea Fishes of the World LifeDesk

Eustomias brevibarbatus is a member of the subgenus Biradiostomias Gomon and Gibbs (1985). Biradiostomias differs from all other subgenera of Eustomias (see Gibbs et al., 1983) in the possession of two long, separate pectoral rays. Dinematochirus, when pectoral fins are present, also has two pectoral rays, but these are closely bound together in black membrane; furthermore, the species of Dinematochirus have a well–developed ventral body groove that extends beyond the pectoral–fin bases, and the barbel is short, usually with a pigmented stem, and usually with branches arising from the stem well before the terminal bulb. Biradiostomias is most similar to the subgenera Nominostomias, Haploclonus, and Eustomias in possessing a relatively long, slender barbel that has little or no external pigment and in lacking a well–developed ventral groove behind the pectoral bases. These three subgenera have three long, separate pectoral rays. Biradiostomias generally is intermediate in photophore, vertebral, anal–ray, and tooth numbers between the higher counts in Nominostomias and Eustomias and the lower counts of Haploclonus. The subgenus Eustomias is unique in having paired photophores in the lateral series. Gibbs et al. (1983, table 1) compare counts of Haploclonus, Biradiostomias (as "2–pectoral–rays"), and Nominostomias.

The following are characters that apply to all species of the subgenus. Two well–developed, free pectoral rays. Seven pelvic rays. Barbel with slender stem having little or no external pigment (axis often pigmented), no row of dark spots, and no branches proximal to terminal bulbs. One to three, rarely four, relatively small terminal bulbs, with or without terminal filaments or projections. No wide ventral body groove posterior to pectoral– fin base. Photophores in ventral series (IC) 69–77 (mostly 71–75), in lateral series (OC) 64– 71 (rarely more than 68, species modes mostly 66–68), VAV and VAL 13–19 (seldom more than 17, species modes 15–17 and 16–17, respectively). Usually 4–6 (rarely 7) VAV photophores located over anal–fin base. No paired photophores in lateral series. Vertebrae in continuous series 63–68 (seldom more than 66, species modes mostly 65–66). Anal rays 31–40, usually 33–38. Premaxillary teeth 7–15; mandibular teeth 9–18 (fewer of each in many specimens less than 100 mm SL).

license
cc-by-nc
copyright
Kenaley, Christopher
author
Kenaley, Christopher

References

provided by Deep sea Fishes of the World LifeDesk

Gibbs RH, Jr, Clarke TA, Gomon JR. 1983. Taxonomy and distribution of the stomioid fish genus Eustomias (Melanostomiidae), I: Subgenus Nominostomias. Smithsonian Contributions to Zoology 380:1–139.

Gomon JR, Gibbs RH, Jr. 1985. Taxonomy and distribution of the stomioid fish genus Eustomias (Melanostomiidae), II: Biradiostomias, new subgenus. Smithsonian Contributions to Zoology No. 409:1–58.

Parr AE. 1927. The stomiatoid fishes of the suborder Gymnophotodermi (Asthronesthidae, Melanostomiatidae, Idiacanthidae) with a complete review of species. Bulletin of the Bingham Oceanographic Collection 3:1–123.

license
cc-by-nc
copyright
Kenaley, Christopher
author
Kenaley, Christopher

Size

provided by Deep sea Fishes of the World LifeDesk

To 152 mm SL.

license
cc-by-nc
copyright
Kenaley, Christopher
author
Kenaley, Christopher

Type locality

provided by Deep sea Fishes of the World LifeDesk

Tongue of the Ocean, Bahamas, 23°55'N, 77°09'W, 4000-7000 feet wire out.

license
cc-by-nc
copyright
Kenaley, Christopher
author
Kenaley, Christopher

Type specimen(s)

provided by Deep sea Fishes of the World LifeDesk

Holotype: YPM 2034.

license
cc-by-nc
copyright
Kenaley, Christopher
author
Kenaley, Christopher

Diagnostic Description

provided by Fishbase
Body slender and elongate, color black; body depth 7.5-10% SL. Head length 10.3-14.4% SL. Lower jaw about equal to length of upper jaw and is not upturned at tip. Long, tapering, protrusible snout. Chin barbel 13-40% SL. Barbel with slender stem and 2-3 terminal bulbs; distal bulb largest and bears 2 or more short, terminal filaments that are variously branched or unbranched. No deep ventral groove (Ref. 37039).
license
cc-by-nc
copyright
FishBase
Recorder
Arlene G. Sampang-Reyes
original
visit source
partner site
Fishbase

Morphology

provided by Fishbase
Dorsal soft rays (total): 20 - 26; Analsoft rays: 33 - 38
license
cc-by-nc
copyright
FishBase
Recorder
Arlene G. Sampang-Reyes
original
visit source
partner site
Fishbase

Biology

provided by Fishbase
Feeds on midwater fishes (Ref. 37039).
license
cc-by-nc
copyright
FishBase
Recorder
Cristina V. Garilao
original
visit source
partner site
Fishbase

Comprehensive Description

provided by Smithsonian Contributions to Zoology
Eustomias brevibarbatus Parr, 1927

Eustomias brevibarbatus Parr, 1927:68, figs. 36A, 40 [holotype and 1 paratype; type-locality 23°55′N, 77°09′W].—Regan and Trewavas, 1930:92, figs. 17B, 74B,C [16 additional specimens, description],—Bertin, 1940:381 [specimen in MNHN].—Morrow and Gibbs, 1964:400–402, fig. 109C,D [in part; references to E. brevibarbatus only; no additional specimens].—Rass, 1971:511 [probably in part; listed for Gulf of Mexico and Caribbean Sea; may include E. variabilis.—Parin and Pokhilskaya, 1974:374 [in part; 4 specimens; not Kurchatov station 1255].—Bekker et al., 1975:305 [in part; specimen from station 1253 only].

DIAGNOSIS.—Two terminal bulbs separated by a short interspace, 0.1%–1.5% SL, about 0.32–2.5 times distal-bulb length. Proximal bulb small, 0.1 %–0.7% SL. Distal bulb 0.4%–l.l% SL, 1–5 times proximal-bulb length, with distinctive black pigment cap on proximal end. Terminal filament short, 0.3%–2.5% SL, without prominent bulblets. Barbel length 13%–33% SL. Stem axis lightly to darkly pigmented. External chevron-shaped or roundish striated areas on stem unpigmented. Paired dorsal spots between occiput and dorsal-fin origin 8.

Character Range(% SL)

Individuals Species means

Predorsal length 80.1-87.4 82.9-84.8

Preanal length 67.2-77.6 72.9-75.0

Prepelvic length 54.5-65.1 58.7-61.3

Head length 9.6-15.1 11.8-13.3

Snout length 3.5-7.2 5.1-5.9

Fleshy-orbit length 1.8-4.7 2.6-3.3

Lower-jaw length 8.9-12.9 10.2-11.5

Upper-jaw length 8.1-12.0 9.3-10.7

Depth behind head 3.9-8.8 5.9-8.0

Greatest depth 3.8-11.3 5.6-8.4

Caudal-peduncle depth 1.2-2.7 1.5-2.0

Pectoral-fin length 2.7-26.4 9.7-13.0

Pelvic-fin length 4.7-18.4 12.9-16.2

Dorsal-base length 9.7-14.7 11.0-13.5

Anal-base length 18.7-26.2 20.9-23.8

Longest premaxillary tooth 0.5-2.3 1.4-1.9

Longest mandibular tooth 0.7-2.0 1.3-1.7

DESCRIPTION.—Barbel length is 13%–30% SL in specimens smaller than 65 mm, 15%–28% in those 65–90 mm, and 23%-33% in those larger than 90 mm. Apparently the increase in relative length occurs at different rates in small specimens, but no further change with growth occurs after about 90 mm SL. The axis of the stem varies from lightly to darkly peppered with melanophores, or streaked with dark pigment, the variation apparently not size related. The chevron-shaped or roundish striated areas on the stem are unpigmented. The axis between the bulbs is darkly peppered or streaked, especially distad where it extends onto the proximal quarter to third of the distal bulb as a black cap. The filament axis is without melanophores or with a few proximally.

Proximal and distal bulbs vary in shape from spheroidal to ovoid. The proximal bulb is 0.1%–0.7% SL, distal bulb 0.4%–1.1% SL and 1–5 times proximal-bulb length, neither bulb changing size relative to SL with growth. Several specimens have non-opaque distal bulbs with a reticulate or dendritic network internally.

The distance between bulbs is 0.5%–1.5% SL in small specimens, decreasing in relative length to 0.1%–0.6% in the largest. The distance is 0.3–2.5% times as long as the distal bulb, with no relation to size of fish.

The terminal filament is short, 0.3%–2.5% SL, 0.4–4.0 times distal-bulb length, apparently not changing with growth. It bifurcates or trifurcates near its base, and occasionally branches again further distad. There are no bulblets in the filament.

The postorbital organs of 12 large males (125–152 mm SL) are 1.4%–2.1% SL, 56%–82% fleshy orbit length. A 134 mm male has a postorbital organ only 1.0% SL, 45% fleshy orbit length, and one 105 mm has an organ 1.2% SL, 43% fleshy orbit length. In one female the organ is 0.9%; in all others it is 0.8% or less.

There are eight paired dorsal spots between occiput and dorsal-fin origin, one beneath the dorsal fin, and one variably present on the caudal peduncle.

In two freshly caught specimens the proximal bulb was yellow, the distal bulb blue.

SIMILAR SPECIES.—Of the species of Biradiostomias with two or more non-contiguous, non-bilobate terminal bulbs, E. brevibarbatus is unique in having a black pigment cap on the proximal ¼– of the distal bulb. Eustomias metamelas also has pigment extending onto the distal bulb but the pigment does not extend as far or as evenly onto the bulb as in brevibarbatus, and the filament is longer (31% SL vs. 0.3%–2.5%). The barbels of both metamelas and dispar are longer (54%–82% SL vs. 13%–33% in brevibarbatus), the distance between bulbs is longer (2.9%–4.4% SL vs. 0.1%–1.5%), and both terminal bulbs are larger (proximal bulb 1.3%–1.6% SL vs. 0.1%–0.7%; distal bulb 1.3%-l.8% SL vs. 0.4%-l.l%). Eustomias hypopsilus and E. variabilis are similar to brevibarbatus in having short barbels and relatively small terminal bulbs, but differ in having a longer interspace between bulbs (1.2%–3.7% SL vs. 0.1%–1.5% SL in brevibarbatus). In addition, hypopsilus lacks a terminal filament that is present in brevibarbatus, and the filament of variabilis usually has bulblets, which brevibarbatus lacks.

DISTRIBUTION.—Eastern Gulf of Mexico, Caribbean Sea, and from 29°N, 80°W (off northern Florida) through the Bahamas, Antilles, and offshore roughly parallel to the coast of South America to about 23°S, extending east to about 30°W off central Brazil (Figure 18).

MATERIAL EXAMINED (14, 13, 45 unsexed).—Holotype: BOC 2034 (?, 63.0), 23°55′N, 77°09′W, 0–∼1062 m (4000–7000 ft wire), 1 Mar 1927.

Paratype: BOC 2033 (?, 52.3), 24°00′N, 77° 17′W, 0–∼910 m (6000 ft wire), 28 Feb 1927.

Non-types: BMNH 1929.7.6.119 (, 145.0), 10°24′N, 54°38′W, 0–∼150 m (300 mw), 1850, 19 Nov 1921. BMNH 1929.7.6.120 (, 132.5), 17°44′N, 64°57′W, 0–∼300 m (600 mw), 0320, 7 Dec 1921. BMNH 1929.7.6.121 (, 135.8), 17°44′N, 64°57′W, 0–∼300 m (600 mw), 0320, 7 Dec 1921. BMNH 1929.7.6.122 (, 125.5), 17°13′N, 64°58′W, 0–∼400 m (800 mw), 1800, 15 Mar 1922. BMNH 1929.7.6.123 (, 105.8), 5°35′N, 51°08′W, 0–∼300 m (600 mw), 1900, 16 Nov 1921.

IOAN uncat. (?, 77.3), 23°13′N, 66°52′W, 0–600 m, 1155–1225, 28 Apr 1962. IOAN uncat. (?, 92.2), 1°26′S, 34°44′W, 0–140 m, 0438–0508, 24 Feb 1964. IOAN uncat. (?, 69.0), 19°10′N, 80°43′W, 0–1000 m, 0648–0904, 19 Mar 1973. IOAN uncat. (?, 71.6), 13°56′S, 32°55′W, 0–200 m, 2254–2315, 2 Feb 1964.

ISH 626/66 (, 146.6), 5°34′S, 26°58′W, 0–320 m, 2000–2315, 20 May 1966. ISH 670/66 (, 105; 2, 156.4–167), 9°41′S, 27°39′W, 0–400 m, 2000–2250, 21 May 1966. ISH 753/66 (3, 144–152.0), 21°00′S, 30°00′W, 0–200 m, 2000–2200, 24 May 1966. ISH 940/68 (, 159.5), 4°43′S, 26°39′W, 0–2000 m, 1155–1215, 4 Feb 1968. ISH 1017/68 (, 143.2), 6°06′S, 27°00′W, 0–560 m, 2240–2310, 4 Feb 1968. ISH 647/74 (, 134.2), 2°27′N, 34°52′W, 0–350 m, 2118–2215, 24 Jul 1974.

MCZ 56601 (3?, 75.–81.4), 16°12′N, 78°00′W, 0–198 m, 0016–0430, 6 Jun 1966. MCZ 56602 (?, 77.1), 12°38′N, 74°11′W, 0–225 m, 1702–2020, 29 May 1966. MCZ 56603 (?, 83.0), 21°11′N, 85° 12′W, 0–170 m, 2003–2327, 10 Jun 1966. MCZ 56685 (?, 114), 0°13′N, 35°44′W, 0–25 m, 2025–2125, 15 Mar 1977. MCZ 56599 (?, 71), 17°07′N, 79°32′W, 0–185 m, 0025–0412, 7 Jun 1966. MCZ uncat. (?, 64.2), 16°38′N, 64°27′W, 0–133 m, 0038–0415, 25 May 1966. MCZ uncat. (?, 72.3), 6°11′N, 37°01′W, 0–120 m, 0115–0315, 21 Mar 1977. MCZ uncat. (?, 89), 23°08′S, 32°22′W, 0–110 mm, 0355–0532, 9 Mar 1967. MCZ uncat. (?, 79.6), 10°48′N, 52°17′W, 0–120 m, 2330–0130, 26 Mar 1977.

MNHN 38–122 (, 100), 23°13′N, 82°21′W, 0–∼25 m (50 mw), 0330, 4 Feb 1922. MNHN 1971–16 (, 128), 14°00′N, 61 °40′W, 0–∼1750 m (3500 mw), 0830, 25 Nov 1921.

TCWC 2651.10(?, 79.6), 24°01′N, 86°52′W, 0–300 in, 1730–1740, 8 Jul 1966.

UMML uncat. (?, 71.2), 25°22′N, 79°28′W, 0–750 m, 1437–1733, 23 Feb 1974. UMML uncat. (, 142.5), 25°05′N, 79°23′W, 0–125 m, 2119–2252, 21 Feb 1974.

USNM 260274 (4?, 76–101.1), 00°11′S, 34°47′W, 0–145 m, 0300–0515, 3 Jul 1971. USNM 260275 (?, 130.2), 09°00′N, 40°53′W, 0–505 m, 0205–0405, 20 Sep 1973. USNM 260276 (, 142), 08°56′N, 46°36′W, 0–475 m, 0055–0257, 22 Nov 1973. USNM 260277 (3?, 71.8–90.0), 00°53′N, 38°59′W, 0–200 m, 0000–0300, 14 Mar 1977. USNM 260278 (?, 75.7), 13° 13′N, 54°49′W, 0–490 m, 2200–2400, 6 Oct 1973. USNM 260279 (?, 74.8), 00°01′N, 37°40′W, 0–130 m, 0045–0345, 15 Mar 1977. USNM 260280 (?, 73.1), 07°02′N, 39°29′W, 0–85 m, 215–2355, 21 Mar 1977. USNM 260281 (?, 66.8), 11°12′N, 53°49′W, 0–100 m, 2330–0130, 27 Mar 1977. USNM 260282 (?, 65), 20°13′N, 84°12′W, 0–495 m, 085–1225, 10 Jun 1966. USNM 260283 (?, 71.7), 27°01′N, 90°02′W, 0–95 m, 0000–0408, 22 Jun 1966. USNM 260284 (?, 80.6), 6°11′N, 37°01′W, 0–85 m, 2100–2300, 20 Mar 1977. USNM 260285 (, 111.0), 00°10′S, 34°43′W, 0–100 m, 0050–0250, 3 Jul 1971. USNM 260286 (, 89.0), 10°48′N, 52° 17′W, 0–140 m, 0335–0530, 27 Mar 1977. USNM 260287 (?, 84.4), 07°43′N, 42°04′W, 0–85 m, 2235–0040, 22 Mar 1977. USNM 260288 (3?, 73.9–92.5), 10°03′N, 49°37′W, 0–120 m, 0250–0505, 26 Mar 1977. USNM 260289 (?, 80.5), 28°58′N, 88° 18′W, 0–∼992 m (545 fm), 27 Oct 1960. USNM 260290 (?, 76.2), 29°11′N, 79°50′W, 0–∼364 m (200 fm), Mar-Apr 1962. USNM 260291 (, 168.7), 7°47′N, 53°53′W, 0–∼695 m (382 fm), 16 Nov 1969. USNM 260300 (, 127.5), 19°56′N, 72°00′W, 0–∼910 m (500 fm), 13 Oct 1963.

ZMUC P201829 (, 137.9), 14°00′N, 61°40′W, 0–∼1750 m (3500 mw), 0830, 23 Nov 1921. ZMUC P201831 (, 147.8), 15°08′N, 61 ° 31′W, 0–∼500 m (1000 mw), 2215, 25 Nov 1921. ZMUC P201832 (, 128.9), 17°59′N, 64°41′W, 0–∼50 m (100 mw), 2355, 8 Dec 1921. ZMUC P201833 (, 132.0), 16°03′N, 62°29′W, 0–∼400 m (800 mw), 2000, 3 Apr 1922. ZMUC P202708 (?, 81.5), 10°24′N, 54°38′W, 0–∼150 m (300 mw), 1850, 19 Nov 1921. ZMUC P202709 (?, 66.1), 17°59′N, 64°41′W, 0–∼150 m (300 mw), 2350, 21 Dec 1921. ZMUC P202710 (?, 56.5), 17°43′N, 64°56′W, 0–∼300 m (600 mw), 0020, 4 Jan 1922. ZMUC P202711 (?, 79.7), 17°13′N, 64°58′W, 0–∼400 m (800 mw), 0040, 16 Mar 1922. ZMUC P202712 (?, 70), 17°43′N, 64°56′W, 0–∼400 m (800 mw), 2315, 24 Mar 1922.
license
cc-by-nc-sa-3.0
bibliographic citation
Gomon, Janet R. and Gibbs, Robert H., Jr. 1985. "Taxonomy and distribution of the stomioid fish genus Eustomias (Melanostomiidae), II : Biradiostomias, new subgenus." Smithsonian Contributions to Zoology. 1-58. https://doi.org/10.5479/si.00810282.409

Diet

provided by World Register of Marine Species
Feeds on midwater fishes

Reference

North-West Atlantic Ocean species (NWARMS)

license
cc-by-4.0
copyright
WoRMS Editorial Board
contributor
Kennedy, Mary [email]

Distribution

provided by World Register of Marine Species
Western Atlantic: including the Antilles

Reference

North-West Atlantic Ocean species (NWARMS)

license
cc-by-4.0
copyright
WoRMS Editorial Board
contributor
Kennedy, Mary [email]

Habitat

provided by World Register of Marine Species
Depth range from 20 - 2000m

Reference

North-West Atlantic Ocean species (NWARMS)

license
cc-by-4.0
copyright
WoRMS Editorial Board
contributor
Kennedy, Mary [email]

Habitat

provided by World Register of Marine Species
nektonic

Reference

North-West Atlantic Ocean species (NWARMS)

license
cc-by-4.0
copyright
WoRMS Editorial Board
contributor
Kennedy, Mary [email]