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Data on Catalog of Fishes

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Description

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Barbel length increases from 22% SL in the smallest specimen (48 mm) to 60%–85% in those longer than 100 mm. All specimens have black pigment in the axis of the stem and between the bulbs, and specimens larger than 80 mm have pigment in at least the proximal axis of the filament. The stem axis is usually quite dark, often becoming lighter distally. Between the bulbs, the pigment is often light or absent proximally, becoming darker distally, and there is often a very dark spot or cap at the base of the distal bulb. The external chevron–shaped or roundish striated areas on the stem are usually prominently pigmented, except in the smallest specimens.

Both proximal and distal bulbs vary in shape from spheroidal to long ovoid, sometimes having the ends flattened or, in one case, widened distally (pear-shaped). The bulbs are relatively small in some small specimens, but by about 70 mm both bulbs have attained dimensions that do not change relative to SL with growth. The proximal bulb in specimens larger than 60 mm is 0.6%–1.5% SL; the distal bulb in all over 70 mm is 0.9%–1.6%. In most specimens, the distal bulb is 1.0–1.6 times as long as the proximal bulb, but in small specimens the ratios are 0.5–2.0.

The distance between terminal bulbs is 2.2%–4.2% SL, apparently not changing with growth, and usually is 2–3 times the length of the distal bulb (in the smallest specimens the interspace is up to 7.8 times the distal bulb).

The terminal filament is long, 22%–33% SL when intact, without apparent change in relative length with growth. Short side branches are present occasionally, arising variously from close to the bulb to well distad on the filament. Four of our specimens had a single such branch, 1 had 2 together. Tiny bulblets are present along the filament axis but are difficult to discern in most specimens; they tend to be slightly larger and more prominent proximally.

The postorbital organs of 7 large males (112–132 mm) are relatively small, 1.2%–1.4% SL, 38%–50% of fleshy–orbit length. A male of 110 mm has an organ only 0.9% SL, indicating that enlargement begins at about this body size.

Beebe and Crane (1939:220) described the colors of the bulbs in a living male from Bermuda. The proximal bulb was translucent white, the distal bulb clear pink. In our observations of 4 males and 3 females from Bermuda and south, the proximal bulb varied from almost white to pink, while the distal bulb was pink to pinkish purple. The postorbital organs were white in both sexes. No sexual dimorphism in color is apparent.

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Description

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Barbel length increases from 22% SL in the smallest specimen (48 mm) to 60%–85% in those longer than 100 mm. All specimens have black pigment in the axis of the stem and between the bulbs, and specimens larger than 80 mm have pigment in at least the proximal axis of the filament. The stem axis is usually quite dark, often becoming lighter distally. Between the bulbs, the pigment is often light or absent proximally, becoming darker distally, and there is often a very dark spot or cap at the base of the distal bulb. The external chevron-shaped or roundish striated areas on the stem are usually prominently pigmented, except in the smallest specimens.

Both proximal and distal bulbs vary in shape from spheroidal to long ovoid, sometimes having the ends flattened or, in one case, widened distally (pear–shaped). The bulbs are relatively small in some small specimens, but by about 70 mm both bulbs have attained dimensions that do not change relative to SL with growth. The proximal bulb in specimens larger than 60 mm is 0.6%– 1.5% SL; the distal bulb in all over 70 mm is 0.9%–1.6%. In most specimens, the distal bulb is 1.0–1.6 times as long as the proximal bulb, but in small specimens the ratios are 0.5–2.0.

The distance between terminal bulbs is 2.2%– 4.2% SL, apparently not changing with growth, and usually is 2–3 times the length of the distal bulb (in the smallest specimens the interspace is up to 7.8 times the distal bulb).

The terminal filament is long, 22%–33% SL when intact, without apparent change in relative length with growth. Short side branches are present occasionally, arising variously from close to the bulb to well distad on the filament. Four of our specimens had a single such branch, 1 had 2 together. Tiny bulblets are present along the filament axis but are difficult to discern in most specimens; they tend to be slightly larger and more prominent proximally.

The postorbital organs of 7 large males (112–132 mm) are relatively small, 1.2%–1.4% SL, 38%–50% of fleshy–orbit length. A male of 110 mm has an organ only 0.9% SL, indicating that enlargement begins at about this body size.

Beebe and Crane (1939:220) described the colors of the bulbs in a living male from Bermuda. The proximal bulb was translucent white, the distal bulb clear pink. In our observations of 4 males and 3 females from Bermuda and south, the proximal bulb varied from almost white to pink, while the distal bulb was pink to pinkish purple. The postorbital organs were white in both sexes. No sexual dimorphism in color is apparent.

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Diagnostic Description

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Two terminal bulbs separated by a long interspace (2.2%–4.2% SL; usually 2–3 times length of distal bulb, but up to 7.5 times in some small specimens). Barbel 60%–85% SL in specimens over 100 mm. Terminal filament long, 22%–33% SL when intact, rarely with 1 or 2 short branches. Distal bulb usually 0.9%–1.6% SL, 1.0–1.6 times length of proximal bulb (0.5–2.0 times in small specimens). Axis of stem pigmented, usually darkly. External chevron-shaped or roundish striated areas on stem usually pigmented in specimens larger than 80 mm. Paired dorsal spots between occiput and dorsal-fin origin usually 8, occasionally 7.

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Diagnostic Description

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Two terminal bulbs separated by a long interspace (2.2%–4.2% SL; usually 2–3 times length of distal bulb, but up to 7.5 times in some small specimens). Barbel 60%–85% SL in specimens over 100 mm. Terminal filament long, 22%–33% SL when intact, rarely with 1 or 2 short branches. Distal bulb usually 0.9%–1.6% SL, 1.0–1.6 times length of proximal bulb (0.5–2.0 times in small specimens). Axis of stem pigmented, usually darkly. External chevron–shaped or roundish striated areas on stem usually pigmented in specimens larger than 80 mm. Paired dorsal spots between occiput and dorsal–fin origin usually 8, occasionally 7.

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Distribution

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Known from the North Atlantic west of 50°W between 25° and 40°N. Two specimens have been taken in the northern Bahamas. The 149.6-mm specimen from north of Puerto Rico recorded by Morrow and Gibbs (1964) was tentatively reidentified as bimargaritatus by Gibbs et al. (1983).

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Distribution

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Known from the North Atlantic west of 50°W between 25° and 40°N. Two specimens have been taken in the northern Bahamas.

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Main Reference

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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.

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Main Reference

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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.

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Morphology

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Eustomias bibulbosus is a member of the subgenus Nominostomias Reagan and Trewavas (1930). The following description from Gibbs et al. (1983) applies to all members of Nominostomias.

Three 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 the terminal bulbs (E. multifilis may have a few short filaments on the stem near the bulb). One or 2 relatively small terminal bulbs, the distalmost with a projection or filament of variable complexity (the projection almost indiscernible in a few species). No wide ventral body groove posterior to pectoral–fin base (a narrow, shallow groove observed in some specimens). Photophore and vertebral counts high. Photophores in ventral series (IC) 69–80 (seldom fewer than 72, species modes mostly 75–78), in lateral series (OC) 63–73 (seldom fewer than 66, species modes mostly 69–72), VAV and VAL 15–21 (seldom fewer than 16, species modes 17–18 and 18– 19, respectively). Vertebrae in continuous series 64–71 (seldom fewer than 65, species modes mostly 67–69). No paired photophores in lateral series. Number of teeth high: premaxillary 11–20, mandibular 14–29 in large specimens (fewer in many specimens less than 100 mm SL).

Counts of fin-rays, photophores, vertebrae, and teeth are of little use in distinguishing most species of Nominostomias, for even those species that show modal differences overlap the ranges of most other species.

None of the body proportions examined by Gibbs et al. (1983) showed convincing differences among species of Nominostomias. Differences in size or relative-growth patterns appeared to characterize a number of species for which few specimens were measured, but these are believed to be artifacts of sampling. The cloud of points of species with abundant measurements usually encompassed those of species with few measurements, and in those abundant species, isometric growth is indicated for almost every body part once metamorphosis is complete. The only body measurement to indicate allometric growth is the least caudal-peduncle depth, which decreases relative to SL.

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References

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Beebe W, Crane J. 1939. Deep–sea fishes of the Bermuda Oceanographic Expeditions. Zoologica (New York) 24:65–238.

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.

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References

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Beebe W, Crane J. 1939. Deep-sea fishes of the Bermuda Oceanographic Expeditions. Zoologica (New York) 24:65–238.

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.

Morrow JE, Jr., Gibbs RH, Jr. 1964. Family Melanostomiatidae. Fishes of the Western North Atlantic 1, pt. 4:351–522.

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.

Regan CT, Trewavas E. 1930. The fishes of the families Stomiatidae and Malacosteidae. Danish Dana Expedition 1920−22 6:1−143.

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Size

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To at least 137 mm SL.

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Size

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To at least 137 mm SL.

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Type locality

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Tongue of the Ocean, Bahamas, 23°58'N, 77°26'W, 7000 feet wire out.

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Type locality

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Tongue of the Ocean, Bahamas, 23°58'N, 77°26'W, 7000 feet wire out.

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Type specimen(s)

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Holotype: YPM 2039.

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Type specimen(s)

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Holotype: YPM 2039.

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Diagnostic Description

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Two terminal bulbs separated by a long interspace (usually 2-3 times length of distal bulb, but up to 7.5 times in some small specimens). Barbel 60-85% SL in over 10 cm specimens. Terminal filament long, rarely with 1 or 2 short branches. Distal bulb usually 1-1.6 times length of proximal bulb (0.5-2 times in small specimens). Axis of stem pigmented, usually dark. External chevron-shaped or striated areas on stem usually pigmented in specimens larger than 8 cm. Paired dorsal spots between occiput and dorsal-fin origin usually 9, sometimes 7 (Ref. 11333).
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Estelita Emily Capuli
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Morphology

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Dorsal soft rays (total): 22 - 25; Analsoft rays: 35 - 42
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Comprehensive Description

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Eustomias bibulbosus Parr, 1927

Eustomias bibulbosus Parr, 1927:70 [25°58′N, 77°26′W].—Regan and Trewavas, 1930:82 [2 additional specimens, N. Sargasso Sea].—Beebe, 1937:199 [lists 8 specimens from Bermuda].—Beebe and Crane, 1939:211, 219–221 [description of same 8 specimens; barbels, fig. 70; E. arborifer in synonymy; E. bimargaritatus tentatively in synonymy].—Grey, 1955:282 [1 specimen from Bermuda].—Morrow and Gibbs, 1964:391 [part; only additional specimen, from north of Puerto Rico, considered herein to be bimargaritatus; E. micraster, bituberatus in synonymy].—Blache et al., 1970:171 [part, fig. 459a only].—Gibbs, 1971:239 [8 additional specimens from Bermuda].

DIAGNOSIS.—Two terminal bulbs separated by a long interspace (2.2%–4.2% SL; usually 2–3 times length of distal bulb, but up to 7.5 times in some small specimens). Barbel 60%–85% SL in specimens over 100 mm. Terminal filament long, 22%–33% SL when intact, rarely with 1 or 2 short branches. Distal bulb usually 0.9%–1.6% SL, 1.0–1.6 times length of proximal bulb (0.5–2.0 times in small specimens). Axis of stem pigmented, usually darkly. External chevron-shaped or roundish striated areas on stem usually pigmented in specimens larger than 80 mm. Paired dorsal spots between occiput and dorsal-fin origin usually 8, occasionally 7.

DESCRIPTION.—Barbel length increases from 22% SL in the smallest specimen (48 mm) to 60%–85% in those longer than 100 mm. All specimens have black pigment in the axis of the stem and between the bulbs, and specimens larger than 80 mm have pigment in at least the proximal axis of the filament. The stem axis is usually quite dark, often becoming lighter distally. Between the bulbs, the pigment is often light or absent proximally, becoming darker distally, and there is often a very dark spot or cap at the base of the distal bulb. The external chevron-shaped or roundish striated areas on the stem are usually prominently pigmented, except in the smallest specimens.

Both proximal and distal bulbs vary in shape from spheroidal to long ovoid, sometimes having the ends flattened or, in one case, widened distally (pear-shaped). The bulbs are relatively small in some small specimens, but by about 70 mm both bulbs have attained dimensions that do not change relative to SL with growth. The proximal bulb in specimens larger than 60 mm is 0.6%–1.5% SL; the distal bulb in all over 70 mm is 0.9%–1.6%. In most specimens, the distal bulb is 1.0–1.6 times as long as the proximal bulb, but in small specimens the ratios are 0.5–2.0.

The distance between terminal bulbs is 2.2%–4.2% SL, apparently not changing with growth, and usually is 2–3 times the length of the distal bulb (in the smallest specimens the interspace is up to 7.8 times the distal bulb).

The terminal filament is long, 22%–33% SL when intact, without apparent change in relative length with growth. Short side branches are present occasionally, arising variously from close to the bulb to well distad on the filament. Four of our specimens had a single such branch, 1 had 2 together. Tiny bulblets are present along the filament axis but are difficult to discern in most specimens; they tend to be slightly larger and more prominent proximally.

The postorbital organs of 7 large males (112–132 mm) are relatively small, 1.2%–1.4% SL, 38%–50% of fleshy-orbit length. A male of 110 mm has an organ only 0.9% SL, indicating that enlargement begins at about this body size.

Beebe and Crane (1939:220) described the colors of the bulbs in a living male from Bermuda. The proximal bulb was translucent white, the distal bulb clear pink. In our observations of 4 males and 3 females from Bermuda and south, the proximal bulb varied from almost white to pink, while the distal bulb was pink to pinkish purple. The postorbital organs were white in both sexes. No sexual dimorphism in color is apparent.

SIMILAR SPECIES.—Only 2 similar species occur near or with E. bibulbosus. Of these bituberatus has a longer barbel at any given size (Figure 6) and apparently always has 2 small branches together on the terminal filament near the distal bulb; only 1 specimen of bibulbosus had 2 branches, and these were well distad on the filament. The terminal bulbs of small bituberatus are larger than in bibulbosus (Figure 7), and the interspace is generally shorter in bituberatus, but there is some overlap (Figure 8). The interspace is 1.5–2.6 times the length of the proximal bulb and 1.0–1.9 times the length of the distal bulb in bituberatus; in bibulbosus these ratios are 2.3–8.5 and 2.0–7.5, respectively.

The terminal filament of micraster has 4 or more short branches close together near the distal bulb, and specimens larger than 100 mm have shorter barbels (less than 60% of SL) and distal bulbs smaller than the proximal (equal or greater in bibulbosus).

The South Atlantic species austratlanticus is very similar to bibulbosus, but apparently has a shorter filament with 2 short branches together a short distance from the distal bulb, and the only large male has a larger postorbital organ (1.7% SL, 57% of fleshy orbit vs. 1.2%–1.4% SL, 38%–50% of fleshy orbit in bibulbosus).

The similar Pacific species bituberoides, bibulboides, orientalis, and australensis have a shorter interspace between the terminal bulbs (Figure 8), and in appositus and inconstans the bulbs are contiguous. Each of these differs from bibulbosus in 1 or more other barbel characters.

DISTRIBUTION.—Known from the North Atlantic west of 50°W between 25° and 40°N. (Figure 40). Two specimens have been taken in the northern Bahamas. The 149.6 mm specimen from north of Puerto Rico recorded by Morrow and Gibbs (1964) is tentatively reidentified as bimargaritatus and discussed under that species.

A juvenile, ∼56 mm SL (USNM 226471), taken at 34°15′N, 28°39′W, cannot be identified satisfactorily. The capture locality is far to the east of any others of bibulbosus and is out of the known range of any species of Nominostomias except longibarba, but the specimen appears to have 2 terminal bulbs and a terminal filament longer than the distal bulb. The range of E. filifer includes the capture locality, but filifer has only 1 well-developed pectoral ray, while this specimen has 3. We are unable to resolve this problem.

MATERIAL EXAMINED (11 males, 14 females, 10 unsexed).—Holotype: BOC 2039 (, 118.4) 23°58′N, 77°26′W, 0 ∼2134 m (7000 ft wire), 2 Mar 1927.

Non-types: USNM 223655 (, 149.0), 36°43′N, 68°09′W, 0–3000 m, 1945, 28 Feb 1978. USNM 223741 (?, 53.4), 32°28′N, 64°02′W, 144–178 m, 2300–0000, 7 Sept 1971. USNM 223742 (, 89.2), 32°19N′, 63°38′W, 0–450 m, 0535–0840, 8 Sep 1969. USNM 223743 (, 115.5), 33°00′N, 64°45′W, 0–1425 m, 4 Jul 1968. USNM 223744 (, 97.0), 32°09′N, 63°59′W, 80–130 m, 0438–0455, 30 Oct 1967. USNM 223745 (, 120.7), 32°13′N, 64°23′W, 100 m, 2205–2305, 1 Jun 1970. USNM 223746 (?, 53.2), 32°22′N, 64°11′W, 210–222 m, 0112–0212, 8 Sep 1971. USNM 223747 (?, 62.0), 32°09′N, 63°59′W, 75–80 m, 0455–0555, 30 Oct 1967. USNM 223748 (?, 73.6), 32°00′N, 64°17′W, 500 m, 0340–0440, 6 Sep 1968. USNM 223749 (2, 134.9, 143.7), 32°25′N, 64°14′W, 0–760 m, 0115–0400, 23 Aug 1971. USNM 223750 (, 80.7), 31°56′N, 63°57′W, 0–1690 m, 2150–0515, 8 Sep 1968. USNM 223752 (?, 47.6), 32°12′N, 64°12′W, 722 m, 1603–1703, 3 Sep 1971. USNM 223753 (3, 115.0, 125.0, 137.0; 3, 132.0, 132.0, 142.5), 32°22′N, 64°04′W, 0–100 m, 2047–2207, 22 Aug 1971. USNM 226471 (?, 56), 34°15′N, 28°39′W, 0–460 m, 0001–0200, 5 Sep 1973. MCZ 56702 (, 123.5), 31°31′N, 67°31′W, 0–135 m, 1907–2137, 10 Dec 1968. MCZ 57018 (?, 81.6), 37°18′N, 63°22′W, 0–250 m, 0008–0343, 15 Dec 1976. MCZ 57020 (, 93.4), 39°49′N, 65°58′W, 500–750 m, 1232–1646, 6 Nov 1977. MCZ 57021 (?, 65.7), 35°31′N, 67°17′W, 0–165 m, 2245–0046, 26 Aug 1967. MCZ 57022 (, 77.8), 32°39′N, 68°41′W, 0–457 m, 1940–0055, 19 Sep 1962. MCZ 57023 (, 82.5), 30°10′N, 67°32′W, 0–217 m, 0440–0625, 28 Nov 1968. ZMUC P202702 (, 134.6), 35°42′N, 73°43′W, 0–∼150 m (300 mw), 2000, 21 May 1922. BMNH 1929.7.6.98 (, 127.6), 27°02′N, 53°39′W, 0–∼550 m (1100 mw), 2300, 30 Apr 1922. FMNH 49853 (?, 123.1), 32°16′N, 64°39′W, 0–275 m, 2050–2300, 14 Jul 1948. ISH 3192/79 (2, 110.2, 117.5; , 120.8), 30°27′N, 66°08′W, 0–1800 m, 0405–0813, 15 Apr 1979. ISH 3193/79 (, 111.7), 26°35′N, 60°29′W, 0–600 m, 1932–2103, 24 Mar 1979. ISH 3194/79 (, 118.2), 26°45′N, 59°00′W, 0–1200 m, 1422–1650, 27 Mar 1979. ISH 3195/79 (, 127.4), 31°01′N, 63°15′W, 0–250 m, 2030–2130, 19 Mar 1979. VIMS 05772 (, 131.7), 29°52′N, 77°09′W, 0–1030 m, 2340–0010, 2 Nov 1979. UMML 16573 (?, 59), 25°36′N, 77°16′W, surface, 23 Jun 1962. UMML 33539 (, 150.0), 24°39′N, 76°30′W, 0–1637 m, 0426–0836, 7 Nov 1974.
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bibliographic citation
Gibbs, Robert H., Jr., Clarke, Thomas A., and Gomon, Janet R. 1983. "Taxonomy and distribution of the stomioid fish genus Eustomias (Melanostomiidae), I: subgenus Nominostomias." Smithsonian Contributions to Zoology. 1-139. https://doi.org/10.5479/si.00810282.380

Distribution

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Slope Water off Georges Bank to the Bahamas

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North-West Atlantic Ocean species (NWARMS)

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Habitat

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nektonic

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North-West Atlantic Ocean species (NWARMS)

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