ArticlePDF Available

A new snailfish, Paraliparis nigellus sp nov (Scorpaeniformes, Liparidae), from the Northern Mid-Atlantic Ridge - with notes on occurrence of Psednos in the area

Authors:

Abstract and Figures

During the international MAR-ECO cruise with R/V G.O. Sars in June and July 2004, among the other topics focusing on the ichthyofauna of the northern Mid-Atlantic Ridge, three specimens of the snailfish genus Paraliparis Collett, 1879 were collected in two bottom trawl hauls at 42 and 51 degrees N, at depths 1950 and 2107 m. The specimens of Paraliparis are a new species, most similar to the P. copei complex. Paraliparis nigellus sp. nov. differs from other members of this group in number of vertebrae, dorsal fin ray counts and body color. In addition, three specimens of Psednos groenlandicus Chernova were collected. Together, they represent the first identified records of Liparidae from the northern part of the Mid-Atlantic Ridge.
Content may be subject to copyright.
PLEASE SCROLL DOWN FOR ARTICLE
This article was downloaded by:
[Chernova, Natalia V.]
On:
21 October 2008
Access details:
Access Details: [subscription number 903256071]
Publisher
Taylor & Francis
Informa Ltd Registered in England and Wales Registered Number: 1072954 Registered office: Mortimer House,
37-41 Mortimer Street, London W1T 3JH, UK
Marine Biology Research
Publication details, including instructions for authors and subscription information:
http://www.informaworld.com/smpp/title~content=t713735885
A new snailfish, Paraliparis nigellus sp. nov. (Scorpaeniformes, Liparidae), from
the northern Mid-Atlantic Ridge - with notes on occurrence of Psednos in the
area
Natalia V. Chernova a; Peter R. Møller b
a Zoological Institute of the Russian Academy of Sciences, St. Petersburg, Russia b Zoological Museum,
Natural History Museum of Denmark, University of Copenhagen, Denmark
Online Publication Date: 01 October 2008
To cite this Article Chernova, Natalia V. and Møller, Peter R.(2008)'A new snailfish, Paraliparis nigellus sp. nov. (Scorpaeniformes,
Liparidae), from the northern Mid-Atlantic Ridge - with notes on occurrence of Psednos in the area',Marine Biology Research,4:5,369
— 375
To link to this Article: DOI: 10.1080/17451000802017507
URL: http://dx.doi.org/10.1080/17451000802017507
Full terms and conditions of use: http://www.informaworld.com/terms-and-conditions-of-access.pdf
This article may be used for research, teaching and private study purposes. Any substantial or
systematic reproduction, re-distribution, re-selling, loan or sub-licensing, systematic supply or
distribution in any form to anyone is expressly forbidden.
The publisher does not give any warranty express or implied or make any representation that the contents
will be complete or accurate or up to date. The accuracy of any instructions, formulae and drug doses
should be independently verified with primary sources. The publisher shall not be liable for any loss,
actions, claims, proceedings, demand or costs or damages whatsoever or howsoever caused arising directly
or indirectly in connection with or arising out of the use of this material.
ORIGINAL ARTICLE
A new snailfish, Paraliparis nigellus sp. nov. (Scorpaeniformes,
Liparidae), from the northern Mid-Atlantic Ridge
with notes on
occurrence of Psednos in the area
NATALIA V. CHERNOVA
1
& PETER R. MØLLER
2
1
Zoological Institute of the Russian Academy of Sciences, St. Petersburg, Russia, and
2
Zoological Museum, Natural History
Museum of Denmark, University of Copenhagen, Denmark
Abstract
During the international MAR-ECO cruise with R/V G.O. Sars in June and July 2004, among the other topics focusing on
the ichthyofauna of the northern Mid-Atlantic Ridge, three specimens of the snailfish genus Paraliparis Collett, 1879 were
collected in two bottom trawl hauls at 42 and 518N, at depths 1950 and 2107 m. The specimens of Paraliparis are a new
species, most similar to the P. copei complex. Paraliparis nigellus sp. nov. differs from other members of this group in number
of vertebrae, dorsal fin ray counts and body color. In addition, three specimens of Psednos groenlandicus Chernova were
collected. Together, they represent the first identified records of Liparidae from the northern part of the Mid-Atlantic
Ridge.
Key words: Liparidae, Mid-Atlantic Ridge, Paraliparis,Psednos
Introduction
One of the goals of the international MAR-ECO
program (Bergstad & Godø 2003; Wenneck et al.
2008) was to study the ichthyofauna of the northern
Mid-Atlantic Ridge. Among the interesting catches
on a cruise on board of the R/V G.O. Sars in June
and July 2004 were three specimens of the snailfish
genus Paraliparis Collett, 1879 and three specimens
of Psednos Barnard, 1927. Both genera were pre-
viously unknown from this area.
Paraliparis includes at least 116 species (Chernova
2007) and is among the most specious genera in
Teleostei (Nelson 2006). It is a derived genus,
adapted for life in the deep sea (Knudsen et al.
2007). Most species are rarely collected and new
species are described frequently (Chernova et al.
2004). Comparisons of the MAR-ECO specimens
with congeners show that they belong to the P. copei
complex but represent a previously unknown spe-
cies. This group of taxa, closely related to Paraliparis
copei Goode & Bean, 1896, were distinguished by A.
Andriashev (1986, 2003). They are characteristic by
having practically uniserial teeth on both jaws, gill
opening reduced to no more than the size of pupil,
opercular flap undeveloped, vertebrae 6574, pec-
toral-fin rays 2023, caudal-fin rays 8, pectoral
radials 4(31), peritoneum and gill cavity black.
Paraliparis copei sensu stricto was described from
the Western North Atlantic (646985 m) (Goode &
Bean 1896) and is also known from the European
continental slope (11001650 m) (Andriashev
2003). The three additional subspecies of this
complex are known from the Southern Hemisphere.
Andriashev (2003) suggested that they could be
valid species. However, their taxonomic rank should
not be changed until the entire genus has been
revised. Paraliparis copei sensu lato includes P. c .
gibbericeps Andriashev, 1982 from South Georgia
(4001000 m) (Andriashev 1982a, 1986, 2003), P. c .
kerguelensis Andriashev, 1982 from off the Kerguelen
Islands and Plateau (at 5801055 m, juveniles at
372613 m) (Andriashev 1982b, 1986, 2003; Cher-
nova & Duhamel 2003), P. c. wilsoni Richards, 1966
from off South Africa, Meteor Seamount, along
Walvis Ridge (9601829 m) (Richards 1966;
Correspondence: N. V. Chernova, Ichthyological Department, Zoological Institute of the Russian Academy of Sciences, Universitetskaya
nab. 1, St. Petersburg, 199034, Russia. E-mail: chernova@zin.ru
Published in collaboration with the University of Bergen and the Institute of Marine Research, Norway, and the Marine Biological Laboratory,
University of Copenhagen, Denmark
Marine Biology Research, 2008; 4: 369375
(Accepted 24 January 2008; Printed 17 October 2008)
ISSN 1745-1000 print/ISSN 1745-1019 online #2008 Taylor & Francis
DOI: 10.1080/17451000802017507
Downloaded By: [Chernova, Natalia V.] At: 07:23 21 October 2008
Andriashev 1986, 2003) and from the Crozet Islands
(7001040 m) (Chernova & Duhamel 2003). Un-
described Paraliparis similar to P. copei are known
from Rio-Grande Seamount (31837?S, 34855?W,
1300 m), northwestern Africa and off Madagascar
(1560 m) (Andriashev 1986, 2003) and the area
northward of Australia (Stein et al. 2001). The
entire P. copei complex is obviously closely related
to P. paucides Stein, 1978 from the Northeast Pacific
and P. rosaceus Gilbert, 1890 from the North Pacific.
Thus, species of P. copei group and their relatives are
widely distributed in the depths of the World Ocean.
The three new specimens from the Mid-Atlantic
Ridge fit in the P. copei complex but differ from
known taxa by the distinctly dark black-brown color,
vertebrae and fin-ray counts, proportions and details
of dentition.
Materials and methods
For description, we follow Stein et al. (2001) and
Chernova & Duhamel (2003). In order to limit
damage to the type specimens, the pectoral-fin girdle
was not removed but the skin and muscles were
dissected and folded over, and the cartilaginous
basal lamina was cleaned of tissue. Meristics were
taken from radiographs; number of vertebrae ob-
tained separately for abdominal and caudal vertebrae
(urostyle included).
The following abbreviations for counts and mea-
surements have been used. Number of rays: A for
the anal fin, C for the caudal fin, D for the dorsal
fin; HL, head length; P, number of rays for the
pectoral fin; SL, standard length; TL, total length;
UPL, upper pectoral-fin lobe; vertebrae, number of
vertebrae.
Comparative materials studied
Paraliparis copei. Holotype USNM 35637, TL
178 mm, SL 167 mm, New Jersey, 39812?17ƒN,
72809?30ƒW, 951 m, Albatross St. 2232, 13 Septem-
ber 1884. Western North Atlantic: four specimens
from two stations (see measurements in Table I):
ZMH 104008, two females SL 142 and 144 mm and
juvenile SL 102 mm, 37828?N, 74820?W, Walther
Herwig St. 198, 14 March 1973, depth 700900 m;
ZMH 104017, female SL 124 mm, Newfoundland
Bank, 45824?N, 48804?W, Walter Herwig St. 273/73,
13 May 1973, depth 17601940 m. Greenland:
more than 40 specimens from 30 stations: ZMUC
P82213, P8241314, P8249697, P82499501,
P82503, P8250507, P82510, P8251213, P82520
and others. Eastern North Atlantic: six specimens
from six stations: ZMH 104039, 104036, 104023,
104025, 104043; ZIN 51112.
Paraliparis copei kerguelensis. Seven specimens, SL
81170 mm from six stations. Kerguelen Island:
Trawler Kerguelen de Tre
´marec, collector J. Maison:
MNHN 1997-13, female SL 170 mm, 1 April 1996,
48801?S, 71838?E, depth 610 m. MNHN 1998-610,
SL 147 mm, 26 January 1998, 48812?S, 71814?E,
depth 655825 m. MNHN 2000-0171, MNHN
2000-0170, subadult female SL 81 mm and male
SL 92 mm, 14 February 1999, 48812?S, 71817?E,
depth 790985 m. MNHN 2000-1380, 137 mm SL,
7 January 2000, 47815?S, 71812?E, depth 450
538 m. MNHN 2000-1381, juvenile SL 83 mm,
15 December 1999, 47816?S, 68859?E, depth 372
613 m. MNHN 2002-1076, SL 128 mm, TL
139 mm, Longliner Antarctic 1, 25 October 2000,
49847?S, 73807?E, depth 9271055 m. Collector J.
Maison.
Paraliparis copei wilsoni. Crozet Island: nine speci-
mens from four stations, SL 3764 mm, RV Marion-
Dufresne: MNHN 1988-66, juvenile SL 62 mm, 28
February 1982, 42852?S, 51806?E, depth 700 m.
MNHN 1988-67, two juveniles SL 45 and 53 mm,
28 February 1982, 45854?S, 51818?E, depth 945
995 m. MNHN 1988-68, four juveniles SL 5464
mm, 18 February 1982, 45844?S, 49820?E, depth
1015 m. MNHN 1988-69, two juveniles SL 37 and
61 mm, 46814?S, 51804?E, depth 10101040 m.
Meteor Seamount: MNHN 1992-1398, female SL
150 mm, TL 165 mm, FRV Evrika, 22 March 1981,
48804?S, 08815?E, depth 960970 m.
For details of P. c. kerguelensis and P. c. wilsoni see
Chernova & Duhamel (2003).
Description
Paraliparis nigellus sp. nov.
(Figures 1, 2)
Paraliparis sp. Bergstad et al. 2008: 191.
Holotype: ZMUB 8485, adult male, TL 136 mm,
SL 124 mm. Mid-Atlantic Ridge, 51845.04?N,
29832.89?W, depth 1950 m. R/V G.O. Sars, cruise
17. St. 56-378, 17 July 2004. Campelen 1800
bottom trawl, 4.5 m vertical opening, and 17 m
horizontal opening; cod-end mesh size 22 mm.
Collector Ingvar Byrkjedal.
Paratype: ZMUB 2633, immature female, TL
88mm (the end of caudal part of body missing),
North of Azores, 42848.6?N, 29838.36?W, 2107 m.
R/V G.O. Sars, cruise 17. St. 42-368, 8 July 2004.
370 N. V. Chernova & P. R. Møller
Downloaded By: [Chernova, Natalia V.] At: 07:23 21 October 2008
Table I. Counts and measurements of species in the Paraliparis copei complex (mean values in parentheses).
P. c. kerguelensis P. c. wilsoni
Counts and measurements P. c. copei
a
P. c. gibbericeps
b
1
b
2
c
1
b
2
c
P. nigellus sp. nov.
a
Counts
Number of specimens 10 8 14 4 19 8 1 (holotype)
Vertebrae 7074 (72) 6771 (69) 6467 (65.5) 6566 (65.5) 6570 (67.5) 6567 (66) 73
Dorsal-fin rays 6367 (65) 5961 (60) 5761 (59) 5961 (60) 5862 (60) 5659 (57.5) 64
Anal-fin rays 5660 (58) 5256 (54) 5054 (52) 5253 (52.5) 5255 (53.5) 5052 (51) 59
Pectoral-fin rays 2124 (22.5) 2122 (21.5) 2022 (21) 2022 (21) 2123 (22) 2022 (21) 25
Caudal-fin rays 8 8 8 8 8 8 8
Measurements
Number of specimens 3 5 4 4 4 1 1 (holotype)
Length, SL mm 124144 94167 95194 128170 125171 150 124
In %SL
Head length 14.515.1 (14.8) 14.917.5 (16.2) 15.316.3 (15.8) 15.616.0 (15.8) 17.218.1 (17.7) 17.3 15.8
Head depth 11.314.2 (12.8) 12.613.6 (13.1) 14.0 14.5
Head width 8.610.4 (9.5) 12.613.6 (13.1) 11.612.6 (12.1) 9.510.9 (10.2) 1213.5 (12.8) 11.3 13.6
Maximum body depth 12.915.1 (14.0) 18.321.7 (20.0) 18.723.2(21.0) 17.222 (19.6) 17.7
Depth above anal-fin origin 10.912.5 (11.7) 14.717.9 (16.3) 15.820.1 (18.0) 14.617.2 (15.9) 14.417 (15.7) 15 13.7
Predorsal length 21.021.6 (21.3) 18.425.5 (22.0) 26 28.4
Preanal length 32.334.7 (33.5) 32.934.5 (33.7) 35.837.1 (36.5) 3742 (39.5) 38 33.5
Mandible to anus 11.814.5 (13.2) 15.016.9 (16.0) 13.415.0 (14.2) 14.216.0 (15.1) 10.816 (13.4) 17 14.9
Anus to anal-fin origin 17.319.4 (18.4) 15.518.2 (16.9) 21.526.3 (23.9) 18.524 (21.3) 20.7 16.1
Upper pectoral lobe length 9.511.1 (10.3) 11.813.8 (12.8) 10.813.7 (12.2) 11.611.9 (11.8) 13.314.6 (14.0) 11.7 10.6
Pectoral-fin notch ray length 2.83.8 (3.3) 4.44.8 (4.6)  2.9
Lower pectoral lobe length 9.710.4 (10.1) 10.210.9 (10.6) 12 11.3
Eye diameter 4.04.5 (4.3) 4.34.9 (4.6) 4.15.6 (4.9) 4.15.0 (4.6) 4.44.7 (4.7) 4.0 4.4
Snout length 4.95.6 (5.3) 4.76.5 (5.6) 4.85.6 (5.2) 6.77.3 (7.0) 6.0 5.8
Interorbital 5.08.0 (6.5) 7.07.4 (7.2) 6.38.1 (7.2) 7.58.8 (8.2) 8.510 (9.3) 9.0 6.2
Gill opening 1.62.1 (1.9) 1.01.4 (1.2) 1.32.1 (1.7) 2.02.3 (2.2) 1.42.0 (1.7) 1.7 2.1
In %HL
Upper pectoral lobe length 6575 (70) 6982 (75.5) 6773 (70) 67
Eye diameter 2831 (29.5) 2527 (26) 2536 (30.5) 2631 (28.5) 2627 (26.5) 23 28
Gill opening 11.014.4 (12.7) 68 (7) 914 (11.5) 915 (12) 5.89.3 (7.6) 9.6 13.3
a
Our data.
b
Data from Andriashev (2003).
c
Data from Chernova & Duhamel (2003).
A new species of Paraliparis 371
Downloaded By: [Chernova, Natalia V.] At: 07:23 21 October 2008
Same gear as for the holotype. Collector Ricardo S.
Santos. The specimen skinned. Several posterior
vertebrae missing.
Non type: ZMUC 2619, damaged specimen, not
suitable for description. Same sample data as for
paratype.
Figure 1. Collection locations for Paraliparis nigellus sp. nov. (m) and Psednos groenlandicus ('). Isobaths represent 1000 m increments.
Figure 2. Paraliparis nigellus sp. nov. Holotype ZMUB 8485, adult male, TL 136 mm, SL 124 mm, Mid-Atlantic Ridge, 1950 m. Fresh
specimen. Photograph: MAR-ECO (http://www.mar-eco.no/).
372 N. V. Chernova & P. R. Møller
Downloaded By: [Chernova, Natalia V.] At: 07:23 21 October 2008
Diagnosis
Vertebrae 73(1261). D 64, A 59, P 2325, C 8.
Pectoral radials 4(31). Teeth simple and uniserial
except near jaw symphysis. Gill opening shorter than
pupil diameter. Opercular flap undeveloped. Head
16% SL. Eye 28% of head length (HL). Symphyseal
mandibular pore one. Pectoral fin with notch rays
not rudimentary. Interneural of the first dorsal-fin
ray between neural spine 6 and 7. Anus behind
vertical through gill opening. Mandible to anus
distance almost equal to length from anus to anal-
fin origin. Color dark black-brown, with bluish tint,
peritoneum black.
Description of the holotype
Principal characters are given in Table I.
Head 6.3 in SL, compressed. Head depth almost
equal to HL. Head width slightly exceeds one-half of
HL. Head dorsal profile widely rounded. Snout
deep, short and slightly protruding. Eye large,
3.6 in HL. Pupil 4/5 eye diameter. Interorbital 1.4
eye diameter. Mouth small, subterminal. Angle of
mouth below eye center. Jaw length about a third of
HL. Teeth simple, uniserial at three-fourth of each
jaw; 24 teeth in one row on upper jaw and 32 teeth in
one row on lower jaw distally; the paratype has 16
and 21 teeth in one row on upper and lower jaw
accordingly. Near jaw symphysis only, teeth form
five to seven very short and oblique rows, of two to
three teeth each. Gill opening pore-like, equal to half
of pupil diameter, entirely above pectoral-fin base.
Opercular flap not developed. Burke’s (1930) pore
formula is 2-6-7-1; sensory pores on head include
two pores in canalis nasalis, five pores in c. infra-
orbitalis, two pores (postorbital and suprabranchial
ones) in c. temporalis and seven pores in c. preoper-
culo-mandibularis. Chin pores open in one oval pore.
Body compressed, caudally elongated and thin at
the end. Dorsal contour of body rounded. Body
depth 5.6 in SL. Dorsal and anal fins low. Dorsal fin
origin above anterior third of pectoral-fin and
between neural spines 6 and 7. Pleural ribs absent.
Hypural one, unslit. Pectoral fin deeply notched,
P 25(1825); pectoral-fin number of the paratype
23(1733). Upper pectoral-fin lobe not reaching
anal-fin origin. Two rays in notch not rudimentary,
entirely covered by fin membrane; length of shortest
notch ray 27% of UPL. Lower lobe of five elongated
rays, maximum length 106% UPL. Upper pectoral-
fin ray inserts above level of eye. In holotype and
paratype pectoral-fin radials 4(31), round, fenes-
trae absent.
Anus opening behind vertical through gill slit,
below first fifth of pectoral-fin length. Mandible to
anus length almost equal to distance from anus to
anal-fin origin. Skin thin, naked, semitransparent;
white musculature visible through it. In fresh speci-
men, gelatinous tissue thick over entire body. Pyloric
caeca 6 (paratype), triangular in shape.
Color. Skin dark black-brown. Cheeks, pectoral base
and sides of body appear paler because white
muscles are visible through transparent skin. Snout,
gill opening, pectoral fins, belly and posterior of
dorsal and anal fins black. Orobranchial cavity and
peritoneum ink-black. Live body color dark blackish
brown with bluish tint, head black, belly bluish black
(Figure 2).
Distribution
Known from two stations on the northern part of the
Mid-Atlantic Ridge, between the Azores and
Charlie-Gibbs Fracture Zone, at depths 1950 and
2107 m.
Etymology
The name derives from ‘nigellus’ (Lat.) blackish,
dark.
Comparisons and discussion
Paraliparis nigellus sp. nov. fits in the P. copei complex
in vertebral number, teeth mainly uniserial, gill
Figure 3. Psednos groenlandicus Chernova, 2001. ZMUB 10135, SL 49 mm, Mid-Atlantic Ridge, 12371296 m. Fresh specimen.
Photograph: MAR-ECO (http://www.mar-eco.no/).
A new species of Paraliparis 373
Downloaded By: [Chernova, Natalia V.] At: 07:23 21 October 2008
opening pore-like, opercular flap undeveloped and
eight caudal-fin rays.
Paraliparis nigellus sp. nov. is similar to the P. c .
copei (Western North Atlantic) in vertebrae, D, A
and P number, but differs from it in its dark black-
brown color (vs. yellowish white, only snout, belly
and fins blackish), teeth at jaw symphysis in few
short rows (vs. entirely uniserial), anus opens mid-
distance from tip of mandible to anal-fin origin (vs.
anus opens 1.4 times closer to tip of mandible than
to anal-fin origin) and longer predorsal length (28.4
vs. 21.022.6% SL).
The new species differs from P. c. gibbericeps
(South Georgia) by more numerous counts (e.g.
vertebrae 73 vs. 6771, D 64 vs. 5961 and P 2325
vs. 2122), black-brown body (vs. white), and teeth
forming a few rows anteriorly (vs. entirely uniserial).
Paraliparis nigellus sp. nov. differs from P. kergue-
lensis (Kerguelen area) in having more vertebrae and
pectoral-fin rays (vertebrae 73 vs. 6467, P 2325 vs.
2022), black-brown color (vs. lilac-rose alive), and
interneural of the first dorsal-fin ray between neural
spine 6 and 7 (vs. 3 and 4 to 5 and 6). It differs also
from P. c. kerguelensis by more posterior position of
anus which opens behind vertical of gill opening,
and mandible to anus length almost equal to
distance from anus to anal-fin origin (vs. 1.5 times
shorter than the latter).
Paraliparis nigellus sp. nov. is different from P. c .
wilsoni (Meteor Seamount to South-West Africa) in
shade of coloration (body dark black-brown vs. light
cream-brown), in having more vertebrae (73 vs. 65
70), teeth forming a few rows anteriorly (vs. uni-
serial), slightly smaller head (16 vs. 1718% SL) and
distance from anus to anal fin origin shorter (16 vs.
18.525% SL).
Except for the nominative P. copei, nine other
Paraliparis are known in the North Atlantic (Collett
1879; Vaillant 1888; Cohen 1968; Andriashev 1993,
1997; Andriashev and Chernova 1997; Chernova
2004). Six of them are black or dark-brown, which
could cause confusion with the new species. Para-
liparis nigellus sp. nov. differs from the latter, in
addition to mainly uniserial teeth and pore-like gill
opening, in the following. It differs from P. abyssorum
Andriashev and Chernova, 1997 (eastern North
Atlantic) in having more vertebrae (73 vs. 6467)
and pectoral fin-rays (25 vs. 17). Paraliparis nigellus
sp. nov. differs from P. bathybius (Collett, 1879)
(cold depths of Norwegian Sea and adjacent waters)
by vertebrae number (73 vs. 6364). It differs from
P. bipolaris Andriashev, 1997 (eastern North Atlan-
tic) in having more caudal-fin rays (eight vs. four),
more pectoral radials (four vs. two), posterior
position of the dorsal-fin origin (fits between neural
spines 6 and 7 vs. 3 and 4) and gill opening shorter
(13 vs. 19% HL). Paraliparis nigellus sp. nov. differs
from P. calidus Cohen, 1968 (Gulf of Mexico) by
mouth horizontal (vs. oblique), pectoral-fin notch
rays not rudimentary (vs. rudimentary), vertebrae
number (73 vs. 6770) and caudal-fin rays (eight vs.
six). Paraliparis nigellus sp. nov. differs from P.
challengeri Andriashev, 1993 (Porcupine Basin,
North-East Atlantic) by simple teeth (vs. with small
lateral lobes), pectoral fin notched (vs. unnotched),
pectoral-fin ray number (25 vs. 16). It differs from
P. edwardsi (Vaillant, 1888) (off Morocco) by pec-
toral-fin upper lobe rays number (18 vs. 1113).
Psednos groenlandicus Chernova, 2001
(Figures 1, 3)
Psednos sp. Bergstad et al. 2008: 191; Sutton et al.
2008: 182.
Material collected during R/V G.O. Sars cruise 17.
ZMUB 1961, SL 37 mm, 52845.46?N, 35856.9?W,
St. 15-342, EGERSUND pelagic trawl (60 m
vertical opening; cod-end mesh size 22 mm), fishing
depth 18002015 m over bottom depth 3707 m.
ZMUB 11460, SL 49 mm, 49851,77?N, 298
37,78?W, St. 53-375, depth 9811003 m, Campelen
1800 bottom trawl (4.5 m vertical opening, 17 m
horizontal opening, cod-end mesh size 22 mm).
ZMUB 10135, SL 49 mm, 51833.5?N, 30818.66?W,
St. 60-379, depth 12371296 m, same gear as for
ZMUB 11460.
All characters studied fit well into the original
description: vertebrae 4748(91038), D 4243,
A 36, C 6; coronal pore absent; 11 temporal and
six preoperculo-mandibular pores present. Pre-
viously, this species was known only from off SW
Greenland (Chernova 2001).
Psednos groenlandicus and P. nigellus represent the
first records of identified Liparidae from the north-
ern part of the Mid-Atlantic Ridge. The same
specimens were recently reported as Psednos sp.
and Paraliparis sp. (Bergstad et al. 2008; Sutton
et al. 2008).
Acknowledgements
The authors greatly appreciate the scientists and
crew of R/V G.O. Sars for the collection of the
specimens. Especially, we are grateful to Ingvar
Byrkjedal (ZMUB, Norway), Franz Uiblein (IMR,
Norway), Ricardo S. Santos (University of the
Azores, Portugal), and Andrey Dolgov (PINRO,
Russia), who took care of the specimens at sea.
The senior author was supported by the Johannes
Schmidt Foundation and by grants RFFI No. 08-04-
00135 and Petersburg Ichthyologic School (No.
374 N. V. Chernova & P. R. Møller
Downloaded By: [Chernova, Natalia V.] At: 07:23 21 October 2008
2304.208.4). We thank Jørgen Nielsen and Tammes
Menne for help and support during Chernova visits
to the ZMUC.
References
Andriashev AP. 1982a. A new species and a new subspecies of
Paraliparis (Liparidae) from western Antarctica. Voprosy Ikh-
tiologii 22(2):17986. Russian. [English translation in Journal
of Ichthyology 22(3):19].
Andriashev AP. 1982b. A review of fishes of the genus Paraliparis
Collett (Liparidae) from the Kerguelen area, subantarctic.
Zoologicheskiy Zhurnal 61(5):71625. Russian with English
summary.
Andriashev AP. 1986. Review of the snailfish genus Paraliparis
(Scorpaeniformes: Liparididae) of the Southern Ocean. Theses
Zoology 7:1204.
Andriashev AP. 1993. Re-evaluation of a neglected species Amitra
liparina Goode, 1881, with a description of the close to it new
species Paraliparis challengeri sp. n. (Scorpaeniformes, Lipar-
idae) from Porcupine Basin (North-East Atlantic). Voprosy
Ikhtiologii 33(5):597601. Russian.
Andriashev AP. 1997. Paraliparis bipolaris sp. n. from the
north-eastern Atlantic closely related to antarctic P. kreffti
(Scorpaeniformes, Liparidae). Voprosy Ikhtiologii 37(2):261
4. Russian. [English translation in Journal of Ichthyology
37(2):1969].
Andriashev AP. 2003. Liparid fishes (Liparidae, Scorpaeniformes)
of the Southern ocean and adjacent waters. Explorations of the
Fauna of the Seas 53(61). St. Petersburg: St. Petersburg State
University. 475 p. (Results of the Russian Antarctic Expedi-
tions; 9).
Andriashev AP, Chernova NV. 1997. Two new liparid fish species
(Liparidae, Scorpaeniformes) from abyssal depths of the east-
ern North Atlantic. Voprosy Ikhtiologii 37(4):43743. Russian.
[English translation in Journal of Ichthyology 37(7):47984].
Bergstad OA, Godø OR. 2003. The pilot project Patterns and
processes of the ecosystems of the northern Mid-Atlantic: aims,
strategy and status. Oceanologica Acta 25(5):21926.
Bergstad OA, Menezes G, Høines A
˚S. 2008. Demersal fish on a
mid-ocean ridge: distribution patterns and structuring factors.
Deep-Sea Research II 55:185202.
Burke CV. 1930. Revision of the fishes of the family Liparidae.
Bulletin of the United States National Museum 150: ixii, 1
204.
Chernova N. 2001. A review of the genus Psednos (Pisces,
Liparidae) with description of ten new species from the North
Atlantic and Southwestern Indian Ocean. Bulletin of the
Museum Comparative Zoology 155(10):477507.
Chernova NV. 2004. A new species of Snailfish (Liparidae)
Paraliparis vaillanti sp. nova from the Northwestern Atlantic,
with the redescription of rare species Paraliparis edwardsi
Vaillant. Voprosi Ikhtyologii 44(2):1359. Russian. [English
translation in Journal of Ichthyology 44(2):1359].
Chernova NV. 2007. Snailfishes (Scorpaeniformes, Liparidae):
diversity, distribution and classification. In: Scientific Reports
on 2006. Abstracts. St. Petersburg: Zoological Institute RAS.
p478.
Chernova NV, Duhamel G. 2003. A new species and additional
records of Paraliparis (Scorpaeniformes: Liparidae) from the
Southern Ocean with a provisional field key to juveniles.
Cybium 27:13751.
Chernova NV, Stein DL, Andriashev AP. 2004. Family Liparidae
Scopoli, 1777 snailfishes. California Academy of Science
Annotated Checklists of Fishes 31:172.
Cohen DM. 1968. The cyclopterid genus Paraliparis, a senior
synonym of Gymnolycodes and Eutelichthys, with the description
of a new species from the Gulf of Mexico. Copeia 2:3848.
Collett R. 1879. Fiske fra Nordhavs-Expeditionens sidste Togt,
Sommeren 1878. Christiania Videnskabs-Selskabs Forhandlin-
der (1878) 14:1106.
Goode GB, Bean TH. 1896. Oceanic ichthyology, a treatise on
the deep-sea and pelagic fishes of the world, based chiefly upon
the collections made by the steamers Blake, Albatross, and Fish
Hawk in the northwestern Atlantic, with an atlas containing
417 figures. Special Bulletin United States National Museum
2:1553, 123 plates.
Knudsen SW, Møller PR, Gravlund P. 2007.Phylogeny of the
snailfishes (Teleostei: Liparidae) based on molecular and
morphological data. Molecular Phylogenetics and Evolution
44:64966.
Nelson JS. 2006. Fishes of the World. 4th ed. Hoboken (NJ): John
Wiley & Sons. 624 p.
Richards WJ. 1966. Paraliparis wilsoni, a new liparid fish from the
Gulf of Guinea. Proceedings of the Biological Society Wa-
shington 79:1714.
Stein DL, Chernova NV, Andriashev AP. 2001. Snailfishes
(Pisces: Liparidae) of Australia, including descriptions of thirty
new species. Records of the Australian Museum 53:341406.
Sutton TT, Porteiro FM, Heino M, Byrkjedal I, Langhelle G,
Anderson CIH, et al. 2008. Vertical structure, biomass and
topographic association of deep-pelagic fishes in relation to a
mid-ocean ridge system. Deep-Sea Research II 55:16184.
Vaillant LL. 1888. Expeditions scientifiques du ‘Travailleur’ et du
‘Talisman’ pendant les annees 1880, 1881, 1882, 1883.
Poissons. Paris: G. Masson. 406 p, 28 plates.
Wenneck TdeL, Falkenhaug T, Bergstad OA. 2008. Strategies,
methods, and technologies adopted on the R.V. G.O. Sars
MAR-ECO expedition to the Mid-Atlantic Ridge in 2004.
Deep-Sea Research II 55:628.
Editorial responsibility: Franz Uiblein
A new species of Paraliparis 375
Downloaded By: [Chernova, Natalia V.] At: 07:23 21 October 2008
... Specimens of all four genera involved in the consideration were studied: Liparis, Careproctus, Paraliparis, Rhodichthys, and Psednos [35][36][37][38][39][40][41][42][43]. Materials of liparid species related to the theme were also researched [44][45][46][47][48]. The subgenera and the species groups in the genus Liparis are given according to the review [39]. ...
... Table 1). [48,110] * Boreal or ( * ) mesopelagic species, which penetrate the marginal Arctic (waters of South Greenland and southwestern part of the Barents Sea). 1 The specimen from off Ireland was later described as P. andriashevi [46]. 2 Psednos rossi was separated in a new genus Aetheliparis Stein, 2012. Additional data are needed to decide on the validity of this genus. ...
Article
Full-text available
The marine ichthyofauna of the Arctic Ocean has an ancestral origin from the Pacific Ocean and, to a lesser extent, from the Atlantic Ocean, which is explained by the amphiboreal concept, developed on groups of fish and invertebrates. Snailfishes (Liparidae) of the Arctic and the North Atlantic are analyzed in the context of this amphiboreal concept. The review is based on the data of many years of research on their taxonomy using various material of morphological differences/similarities of the taxa and patterns of species distribution against the background of biogeographic representations. For the Arctic area, 33 species of the family are known: Liparis (5), Careproctus (21), Paraliparis (2), Rhodichthys (2), and Psednos (3). For the Atlantic fauna, with the same number of species, their composition differs: Liparis (6), Careproctus (3), Paraliparis (12), Psednos (11), and Eutelichthys (1). The amphiboreal concept explains the speciation of Liparis and the majority of Careproctus as the result of trans-Arctic preglacial migrations. For other (deep-sea) species, the hypothesis of a transoceanic dispersal route is applicable; it passed from the North Pacific through the Southern Ocean and then north across the Atlantic.
... Snailfishes display an array of interesting adaptations to distinct marine environments, including an antifreeze protein in the skin of Antarctic species (Evans and Fletcher 2001;Hobbs and Fletcher 2013), ossicles that may offer protection with minimum additional weight (M€ arss et al. 2010), and a subdermal extracellular matrix for increasing buoyancy and maintaining ideal body shape for drag reduction (Eastman et al. 1994;Gerringer et al. 2017a). The snailfishes are an understudied group, with many new species still being described (Chernova et al. 2004;Orr 2004;Chernova and Møller 2008;Stein and Drazen 2014) and with several species-level identifications and generic allocations still contentious (Kai et al. 2011;Orr et al., Accepted Manuscript.). ...
Article
Full-text available
Synopsis Deep-sea trenches, depths 6000–11,000 m, are characterized by high pressures, low temperatures, and absence of sunlight. These features make up the majority of the deepest marine habitat—the hadal zone—home to distinct communities from those in the surrounding abyssal plains. The snailfishes, family Liparidae (Scorpaeniformes), have found notable success in the hadal zone from ∼6000 to 8200 m, comprising the dominant ichthyofauna in at least six trenches worldwide. The hadal fish community is distinct from the abyssal community where elongate, scavenging fishes such as rattails (Macrouridae), cutthroat eels (Synaphobranchidae), tripodfishes (Ipnopidae), eelpouts (Zoarcidae), and cusk eels (Ophidiidae) are most common. Until recently, little was known about the biology of these deepest-living fishes, or the factors that drive their success at hadal depths. Here, I review recent investigations spanning the abyssal–hadal boundary and discuss the factors structuring these communities, including the roles of pressure adaptation, feeding ecology, and life history. Hadal fishes show specialized adaptation to hydrostatic pressure both in accumulation of the pressure-counteractant trimethylamine n-oxide and in intrinsic changes to enzymes. Stomach content and amino acid isotope analyses, and jaw morphology suggest that suction-feeding predatory fishes like hadal liparids may find an advantage to descending into the trench where amphipods are increasingly abundant. Analysis of otolith growth zones suggest that snailfishes may be adapted to a seismically active, high-disturbance hadal environment by having relatively short life-spans. This review synthesizes the known literature on the planet’s deepest-living fishes and informs new understanding of adaptations to life in the trenches.
... Paraliparis, 26 species 233-2150 [65,66] [ 5,11,65-67] ...
Article
Full-text available
Many deep-sea fishes have a gelatinous layer, or subdermal extracellular matrix, below the skin or around the spine. We document the distribution of gelatinous tissues across fish families (approx. 200 species in ten orders), then review and investigate their composition and function. Gelatinous tissues from nine species were analysed for water content (96.53 ± 1.78% s.d.), ionic composition, osmolality, protein (0.39 ± 0.23%), lipid (0.69 ± 0.56%) and carbohydrate (0.61 ± 0.28%). Results suggest that gelatinous tissues are mostly extracellular fluid, which may allow animals to grow inexpensively. Further, almost all gelatinous tissues floated in cold seawater, thus their lower density than seawater may contribute to buoyancy in some species. We also propose a new hypothesis: gelatinous tissues, which are inexpensive to grow, may sometimes be a method to increase swimming efficiency by fairing the transition from trunk to tail. Such a layer is particularly prominent in hadal snailfishes (Liparidae); therefore, a robotic snailfish model was designed and constructed to analyse the influence of gelatinous tissues on locomotory performance. The model swam faster with a watery layer, representing gelatinous tissue, around the tail than without. Results suggest that the tissues may, in addition to providing buoyancy and low-cost growth, aid deep-sea fish locomotion.
... Fossen et al. (2008) studied the fish assemblage composition caught by longlines by the MS Loran. Other MAR-ECO fish studies included: the distribution and reproductive biology of Antimora rostrata and Halosauropsis macrochir (Fossen & Bergstad 2006;Bergstad et al. 2012) and of some deepwater skates Orlov & Cotton 2011Orlov 2011); the trophic ecology of Coryphaenoides rupestris (Bergstad et al. 2010), Bathylagus euryops (Sweetman et al. 2013), Myctophidae (Hudson et al. 2014), and Stomiiformes (Carmo et al. 2015); a comprehensive paper on the occurrence and distribution of Macrouridae (Bergstad et al. 2008b); the descriptions of new species (Byrkjedal & Orlov 2007;Chernova & Møller 2008;Byrkjedal et al. 2011); the identification of Synaphobranchus eels (Svendsen & Byrkjedal 2013); the restoration of species relegated to synonymy (Uiblein et al. 2008); new distribution ranges of rare species (Iwamoto & Orlov 2006; the vertical distribution and behaviour of fishes attracted to landers (King et al. 2006); the biological significance of pelagic fishes size structure (Heino et al. 2008a, b); parasitological investigations of various deepwater fishes (Kritsky & Klimpel 2007;Klimpel et al. 2007Klimpel et al. , 2008Busch et al. 2008;Kellermanns et al. 2009); the structure and distribution of midwater fishes associated with the Subpolar front (Cook et al. 2013;Sutton et al. 2013), and selectivity of the pelagic gears used during the main MAR-ECO survey (Heino et al. 2011). ...
... Fossen et al. (2008) studied the fish assemblage composition caught by longlines by the MS Loran. Other MAR-ECO fish studies included: the distribution and reproductive biology of Antimora rostrata and Halosauropsis macrochir (Fossen & Bergstad 2006;Bergstad et al. 2012) and of some deepwater skates Orlov & Cotton 2011Orlov 2011); the trophic ecology of Coryphaenoides rupestris (Bergstad et al. 2010), Bathylagus euryops (Sweetman et al. 2013), Myctophidae (Hudson et al. 2014), and Stomiiformes (Carmo et al. 2015); a comprehensive paper on the occurrence and distribution of Macrouridae (Bergstad et al. 2008b); the descriptions of new species (Byrkjedal & Orlov 2007;Chernova & Møller 2008;Byrkjedal et al. 2011); the identification of Synaphobranchus eels (Svendsen & Byrkjedal 2013); the restoration of species relegated to synonymy (Uiblein et al. 2008); new distribution ranges of rare species (Iwamoto & Orlov 2006; the vertical distribution and behaviour of fishes attracted to landers (King et al. 2006); the biological significance of pelagic fishes size structure (Heino et al. 2008a, b); parasitological investigations of various deepwater fishes (Kritsky & Klimpel 2007;Klimpel et al. 2007Klimpel et al. , 2008Busch et al. 2008;Kellermanns et al. 2009); the structure and distribution of midwater fishes associated with the Subpolar front (Cook et al. 2013;Sutton et al. 2013), and selectivity of the pelagic gears used during the main MAR-ECO survey (Heino et al. 2011). ...
Article
Full-text available
Records of the fishes from the northern Mid-Atlantic Ridge (MAR) (41⁰N - 60⁰N) sampled during two research cruises conducted in summer 2004 on the R/V G.O. Sars and M/S Loran are presented. The cruises were major sampling efforts carried out for the MAR-ECO project, i.e. the Census of Marine Life field project entitled “Patterns and Processes of the Ecosystems of the Northern Mid-Atlantic”. The investigation included sampling with several midwater nets, bottom trawl and longlines from surface waters to about 4000 m. The list comprises around 300 species of fishes from 82 families. Many records were new to the northern mid- Atlantic area, and the list also comprises three recently described species and some additional specimens to date only identified to genus.
... Следует отметить, что в роде Paraliparis известна одна видовая группа -это "P. copei", в которую вхо дит ряд географических форм, сходных с P. copei Goode et Bean, 1896, но имеющих заметные разли чия в пигментации, числе позвонков и некоторых пропорциях тела (Андрияшев, 2003 (Chernova, Møller, 2008). ...
Article
Full-text available
We examine the main drivers that may elevate biomass and biodiversity of non-chemosynthetic benthic megafauna of the lower bathyal (800-3500m depth) of the Mid-Atlantic Ridge in the North Atlantic Ocean (MAR). Specifically: 1. Primary production in surface waters (10°-48°N) from remote sensing data 2002-2020 over the MAR was not significantly different from abyssal regions to the east and west. We reject the hypothesis that presence of a mid ocean ridge may enhance surface primary production. 2. The quantity of particulate organic matter reaching the sea floor was estimated as a proportion of surface export production scaled by bathymetry. Flux was 1.3 to 3.0 times greater on the MAR as a function of shorter vertical transport distance from the surface than on adjacent abyssal regions. 3. Depth variation effect on species richness. Demersal fishes living between 41° and 60°N showed a maximum of species richness at 2000 m depth and linear increase in regional (Gamma) diversity of 32 species per 1,000 m elevation of the MAR above the abyss. Elevated topography provides niches for species that cannot otherwise survive. 4. Substrate heterogeneity. The MAR >95% covered with soft sediment with frequent hard rocky patches spaced at a mean nearest neighbour distance of <500 m. Over 90% were <1 km apart. Animals are readily able to disperse between such patches increasing biodiversity through the additive effect of soft and hard substrate fauna on the MAR. 5. Presence of a biogeographic overlap zone. The MAR harbours bathyal species known from Western Atlantic and Eastern Atlantic continental slopes with meridional asymmetry resulting in bias toward predominance of Eastern species. The mix of species contributes to increased diversity to the east of the MAR. Multiple factors support increase in biomass and biodiversity on the MAR. Biological data are almost entirely absent from 12° to 33°N, the part of the MAR which may be mined for polymetallic sulphide ore deposits. This study enables some predictions of biomass and biodiversity but there is urgent need for intensive biological sampling across the MAR throughout the proposed mining areas south of the Azores.
Article
A new liparid fish, Paraliparis ruficometes sp. nov., is described from 28 specimens collected between 1,430–2,070 m depth in Suruga Trough, Suruga Bay, Japan. It can be distinguished from all currently recognized congeners by the following combination of characters: 61–64 total vertebrae; 53–59 dorsal-fin rays; 48–52 anal-fin rays; 20–25 pectoral-fin rays, lower part of each ray completely free; 6 principal caudal-fin rays, dorsalmost elongate, about 2 or 3 times length of other rays; simple teeth on both jaws; gill slit 5.9–10.0% SL, extending in front of 9th–13th pectoral-fin ray base; 4 pectoral proximal radials (all unnotched); peritoneum and stomach black.
Article
Full-text available
Deep-sea demersal fish surveys using baited cameras were undertaken in the West African oil provinces between 1297 m and 2453 m in 2002, 2005 and 2008. A total of 29 deployments amounting to 16,175 images encountered 31 species of bait attending deep-sea fish from 17 families. The extrapolated species richness was 34, indicating that the survey encountered over 90% of bait attending fish species in this area. The dominant species in the area were the morid Antimora rostrata, the synaphobranchids Synaphobranchus cf. kaupii and Simenchelys parasitica, the somniosid Centroscymnus coelolepis and the zoarcid Pachycara crassiceps. An unusually high diversity of bait attending macrourids was observed in addition to patchy aggregations of zoarcids. This study serves as baseline survey data on which to base future long-term environmental monitoring of fish populations in the vicinity of the West African oil provinces.
Article
Full-text available
Examination of all available liparid specimens collected in Australian waters revealed more than 30 new species in three genera: Careproctus Kroyer, Psednos Barnard, and Paraliparis Collett. This is the first published description of liparids from Australia. The new species include Careproctus
Article
Full-text available
A small collection of liparid fishes was made by French scientific or fishing cruises off the Kerguelen and Crozet Islands in the recent years. A new species, P. obliquosus sp. n., is described. Other species collected included: Paraliparis copei kerguelensis, P. copei wilsoni, P. gracilis, P. neelovi with a closely related form designated as P. cf. neelovi, P. operculosus, P. thalassobathyalis, and also one young fish of an undescribed species, Paraliparis sp. Additional diagnostic characters were found for P. copei wilsoni and P. copei kerguelensis. They include: chin pores open separately (vs in a common pit), interneural of the first dorsal ray situated between vertebrae 5/6 to 8/9 (vs between 3/4 to 5/6), skin of specimens in alcohol cream-brown (vs milky pale), chin and snout blackish-brown (vs pale), anus slightly behind a vertical through the gill opening (vs slightly in front of it). The Crozet islands constitute an extension of the geographical distribution and of the bathymetric range (700-1040 in vs 960-1134 m) for P.c. wilsoni. Some differences in Paraliparis gracilis were found between specimens from South Georgia (Atlantic sector of Southern Ocean) and those from the Crozet islands (Indian sector). Paraliparis operculosus occurred deeper than previously (1129-1295 m vs 380-1010 m). Paraliparis thalassobathyalis appeared polymorphic, with three different types, mainly recognized by the shape of head and body and colour patterns. They might represent sexual dimorphic differences, or epibenthic and pelagic forms, although our material was insufficient for final conclusion. Juveniles of 13.2-44.0 mm SL of P. obliquosus, P. neelovi, P. cf. neelovi, P. operculosus, P. thalassobathyalis and Paraliparis sp. were found pelagically. A field key to early juveniles of the nine Paraliparis is proposed.
Article
Full-text available
Snailfishes are a large and morphologically diverse family of marine fishes within the order Scorpaeniformes. Abundant and speciose in temperate and cold regions of the Pacific and Atlantic, in polar waters, and in the deep sea, snailfishes occur from the intertidal to the maximum depth known for fishes of 7,587 m. They are one of the most speciose families of fishes in the Southern Ocean, the North Pacific, and the Arctic. They also occur in the deep Indian Ocean, but only a few species are known from there. The checklist treats 334 species and 29 genera as valid. We expect many more species to be described.
Article
Gymnolycodes Vaillant and Eutelichthys Tortonese are shown to be junior synonyms of Paraliparis Collett. A diagnosis and a second record are presented for P. leptochirus, the type-species of Eutelichthys. P. calidus new species from the northern Gulf of Mexico is described and compared with its closest known relative, P. bathybius of polar seas.
Article
Mid-ocean ridges offer diverse habitats to benthic and benthopelagic fish, and the species-specific patterns of abundance and distribution as well as community patterns have not been extensively studied. Analyses were conducted of the demersal fish on the Mid-Atlantic Ridge using bottom trawl data from the 2004 R.V. G.O. Sars expedition to the ridge segment north of the Azores (42°N) to south of Iceland (54°N). Overall fish biomass and abundance declined with depth from the summit of the ridge to the middle rises on either side. Sixty-nine species were recorded in the 17 trawls used in the analyses, but several specimens could only be determined to genus level, and the real species number is probably around 80. Multivariate analyses revealed that the species composition primarily changed with depth, and that variation by latitude was secondary. The latitudinal variation was greater in shallow than in deep areas. Cross-ridge differences were apparently minor, but pairwise comparisons of stations at the same depth and latitude on either side of the central rift valley indicated that such differences may occur. The number of species was inversely related to latitude, but declined with depth below the slope depths. Evenness was higher in deep slope and rise areas than on the slopes. Assemblages of species could be defined for different depth zones and sub-areas, but there was no clear zonation by depth. Individual depth and latitudinal ranges of the different species produced the patterns. Temperature, salinity, and oxygen concentration were similar at all trawling locations, and other factors varying more strongly with depth and latitude appear to influence the distribution patterns of individual species and assemblage structure. A general decline in food availability with depth may explain the decrease in abundance and biomass with depth. A difference in pelagic productivity and species composition of zooplankton and pelagic nekton between the areas north and south of the Sub-polar Front may underlie the latitudinal change in abundance and species composition.