BREVIORA
MUSEUM OF COMPARATIVE ZOOLOGY
Harvard University
Numbers 265-295
1967-1968
CAMBRIDGE, MASS.
1969
U.S.A.
^^ ^^
Edited
by
Nelda
E.
Wright
CONTENTS
BREVIORA
Museum
of Comparative Zoology
Numbers 265-295
1967
No. 265.
New
land-locked
fish
North Auckland,
1
No. 266.
1
pp. April
A new
species of the genus Galaxias from
New
Zealand.
By
R.
M. McDowall
6.
species of
Vesicomya from the Caribbean Sea
By Kenneth
(Mollusca: Bivalvia:
Vesicomyidae).
Jay Boss. 6 pp. April 6.
No. 267.
A
new
generic arrangement for some Australian scincid
By Allen E. Greer. 19 pp. June 29.
lizards.
No. 268 The
ecology and behavior of two sympatric Lyeodactylus
geckos. By Allen E.Greer.
9 pp. June 29.'
1
No. 269.
Two new species
of Aniphitarsus
(Ophiuroidea)
Western North Atlantic.
June 29.
No. 270. Additions
By
Amy
'
to the unionid fauna of the
from the
Schoener 9 pp
^^'
Gulf drainage of
Alabama, Georgia, and Florida (Mollusca:
Bivalvia)
By Richard I. Johnson. 21 pp. June 29.
No. 271. Chelonia
depressa Garman re-investigated.
By Ernest
E. Williams, Alice G. C.
Grandiso^n. and Archie F.
Carr,
Jr.
15 pp.
November
17.
No. 272. The
ecological distribution of the anoline lizards around
Kingston. Jamaica. By A. Stanley Rand
18 pp
November
17.
No. 273. Studies on
neotropical Pompilidae (Hymenoptera). III.
Additional notes on
Epipompilus Kohl. By Howard
E.Evans. 15 pp. November 17.
No. 274. The genus Nops (Araneae, Caponiidae) in Panama and
the West Indies. By Arthur M. Chickering. 19 pp.
November
No. 275.
A
17.
new
By
scincid lizard from the northern Solomon Islands.
Allen E. Greer and Fred Parker. 20 pp. Novem-
ber 17.
No. 276. The generic relationships of the African scincid genus
Eumecia. By Allen E. Greer. 9 pp. November 24.
No. 277. Lestidiuni bigelowi,
photophores.
new
a
species of paralepidid fish with
By Michael
J.
F. Graae.
10 pp. No-
vember 24.
No. 278. Notes on the emberizine sparrow Rhynchospiza stolzinanni. By Raymond A. Paynter, Jr. 6 pp. November 24.
No. 279.
A
second skink with fragmented head scales from BouSolomon Islands. By Allen E. Greer and
Fred Parker. 12 pp. November 24.
gainville,
1968
No. 280. The notatus group of Sphaerodactyhis (Sauria, Gekkonidae) in Hispaniola. By Benjamin Shreve. 28 pp.
March
No. 28
1
.
19.
Additional notes on batoid fishes from the Western Adantic.
By Henry B. Bigelow and William C. Schroeder.
23 pp. April
5.
No. 282. The extinct baboon, Porapapio jonesi, in the early Pleistocene of northwestern Kenya. By Bryan Patterson.
4 pp. April 5.
No. 283. Scythian ammonoids from Timor.
mel.
21 pp.
April
By Bernhard Kum-
5.
No. 284. The relationships of Arwlis of the roquet species group
III.
(Sauria: Iguanidae)
Comparative study of
behavior.
By George C. Gorman. 31 pp.
display
—
April
5.
No. 285. The genera of puffbirds (Bucconidae).
trell.
5 pp.
April
5.
By G. W. Cot-
No. 286. The status of Nesogalaxias neocaledonicus (Weber and de
Beaufort) (Pisces. Galaxiidae). By R. M. McDowall.
8 pp.
April
5.
No. 287. The sequence of genera in the Estrildidae (Aves).
Ernst Mayr. 14 pp. April 5.
By
No. 288. The epidermal glands of Lygodactylus (Gekkonidae,
Lacertilia). By P. F. A. Maderson. 35 pp. May 29.
No. 289. The genus Miagrammopes (Araneae, Uloboridae) in
Panama and the West Indies. By Arthur M. Chickering. 28 pp. May 29.
No. 290. Geographic Variation in the Hispaniolan frog Eleutherodactylus wetmorei Cochran.
By Albert Schwartz.
13 pp.
No. 291.
A
new
May
29.
species of Tribolonotiis (Lacertilia:
Scincidae)
from Bougainville and Buka, Solomon Islands, with
comments on the biology of the genus. By Allen E.
Greer and Fred Parker. 23 pp. May 29.
No. 292. Herpetogeography of Puerto Rico. V. Description of a
new species of Sphaerodactylus from Desecheo Island.
By Harold Heatwole. 6 pp. May 29.
No. 293. Intra- and interspecific chromosome variation in the lizard
Anolis cristatellus and its closest relatives. By George
C. Gorman. Richard Thomas, and Leonard Atkins.
13 pp.
May
29.
No. 294. Distribution and biology of the opisthoproctid fish Winteria telescopa Brauer 1901. By Richard L. Haedrich
and James E. Craddock. 1 1 pp. May 29.
No. 295. The Chaiiares (Argentina) Triassic reptile fauna. IV.
The dicynodont fauna. By C. Barry Cox. 27 pp.
May
29.
INDEX OF AUTHORS
BREVIORA
Museum of Comparative Zoology
Numbers 265-295
1967-1968
No.
Atkins, Leonard
293
Bigelow, Henry B
28 1
Kenneth Jay
266
Boss,
Carr, Archie
Chickering,
F.,
271
Jr
Arthur
Cottrell, G.
M
W
274, 289
285
Cox, C. Barry
295
Craddock, James E
294
Evans,
Howard E
273
Gorman, George C
Graae, Michael
284, 293
F
J.
Grandison, Alice G.
277
C
Greer, Allen E
27
1
267, 268, 275, 276. 279. 291
Haedrich, Richard L
294
Heatwole, Harcld
292
Johnson, Rich \rd
2 73
1
No.
KUMMEL, Bernhard
Maderson,
p. F.
283
a
288
Mayr, Ernst
McDowell,
287
R.
M
265, 286
Parker, Fred
275, 279, 291
Patterson, Bryan
Paynter,
Raymond
282
A.. Jr
Rand, A. Stanley
ScHOENER,
278
272
Amy
269
schroeder, william
c
281
Schwartz, Albert
290
Shreve, Benjamin
280
Thomas, Richard
293
Williams, Ernest
E
271
BREVIORA
Mmseuim of Coimparsitive Zoology
Cambridge, Mass.
Number 265
6 April, 1967
NEW
LAND-LOCKED FISH SPECIES
OF THE GENUS GALAXIAS
FROM NORTH AUCKLAND, NEW ZEALAND'
R.
Museum
M. McDowall
of Comparative Zoology, Harvard University
Abstract: Two species of Galaxias Cuvier (Galaxiidae) are described
from small land-locked coastal dune lakes in North Auckland, New Zealand.
They are small shoaling species similar to and apparently derived from the
sea-going Galaxias maculatus attenuatiis (Jenyns).
INTRODUCTION
In the New Zealand Galaxiidae, speciation appears to be taking
place by the land-locking of sea-going species. This is a pattern
familiar in the Northern Hemisphere Salmonidae, and also in the
Southern Hemisphere in the Retropinnidae (McDowall, 1965).
Stokell (1964) described a new species of Galaxias (G. parrishi),
which he considered to be a land-locked derivative of G. maculatus
ignotus, and noted another land-locked form from Victoria, Australia.
The writer (McDowall, 1966) noted a similar form collected from another Victorian lake (see Pollard, 1964), and the
occurrence of further such derivatives from G. maculatus attenuatus, in New Zealand coastal lakes.
About 15 years ago, the New Zealand Marine Department conducted a survey of the chain of small lakes on the west coast of
the North Island of New Zealand, to determine their ecology in
relation to the introduction of suitable
on
game
fishes.
In their report
(1953) described the fish faunas
of these lakes as follows: "Various species of Galaxias, Gobiomorphus, and Retropinna were recorded," and they listed in a table
In 1963, the
the lakes from which these genera were taken.
writer examined a sample of G. maculatus attenuatus-Vike fishes
from one of these lakes, which, on close examination, appeared to
1
this survey,
Cunningham
et al.
Fisheries Research Publication
No.
93.
BREVIORA
No. 265
be distinct from G. maculatus attenuatus in a number of details.
Because this sample was rather old, it was felt desirable to recollect the fish, before description,
and
this
was done
in
March
Galaxias were collected from Lake
Large samples
Waiparera, a few miles north of Kaitaia, and from Upper Lake
Rototuna, on the peninsula west of the northern arm of Kaipara
1965.
of
Harbor (Fig. 1). Inasmuch as these lakes are land-locked, it
was to be expected that the Galaxias populations would differ morphologically and behaviorally from Galaxias maculatus attenuatus.
L
Figure
of:
1.
WAIPARERA-
1.
Locality
of North Island,
Lake Rototuna.
map
Lake Waiparera,
2.
New
Zealand, showing location
Being land-locked, their life cycles are also necessarily modified
from that of G. maculatus attenuatus which has marine juveniles.
Examination of the fresh samples from these two lakes, showed
them to be distinct from G. maculatus attenuatus and from each
other. They do not resemble any other New Zealand species of
Galaxias. Characters suggesting relationship to G. maculatus attenuatus, apart from their general appearance and coloration, include shoaling behavior as adults, forked caudal fins, similar dentition, lack of pyloric caeca,
and the long, many-rayed anal
fin.
NEW
1967
SPECIES OF GALAXIAS
3
The
isolation of sea-going species in small lakes, as
appears to
in these instances,
poses a problem in species
delimitation. The alternatives lie between
each isolate
have taken place
describing
as a distinct species or subspecies, or including all the
populations
in a single, widely variable
species, derived from the parent sea-
Since there has been a fundamental change in the
history pattern of the land-locked species, it seems likely that
going species.
life
and derivative species have acquired reproductive isomechanisms. This conclusion is supported by the fact that
the derivative populations have
developed characteristic morphothe parent
lating
logical differences from the parent population. The specific distinctness of the two derivative populations under examination is
another problem.
studies of the
Ideally,
breeding experiments and behavioral
two populations would be desirable
to provide the
answers, but these are outside the scope of the present study. On
examining the morphological differences between the two populations, it seemed likely that they were independently derived from
the parent stock and therefore more
closely related to the parent
than to each other. The population in Lake Rototuna is, from both
morphological and geological considerations, probably an earlier
derivative of G. maculatus attenuatus than is the Lake Waiparera
population. Lake Rototuna occurs in well stabilized rolling sand
dunes, once covered in bush, at an altitude of 300 ft. (91 m).
whilst Lake Waiparera is in still shifting sand dunes, about a hundred feet (36 m) above sea level. Corresponding to their apparent
difference in age, and perhaps to differing ecological conditions in
the two lakes, the degree to which these species have diverged
from their common parent species differs greatly. The differences
are most obvious in vertebral count, a character which has proved
useful in separating Galaxias species in New Zealand. Assuming
relationship to G. maculatus attenuatus, the Lake Rototuna population has traversed the full range of vertebral number in the New
Zealand Galaxiidae, from the maximum in G. maculatus attenuatus
minimum of 47-50. The vertebral number in the
Lake Waiparera population is also reduced and almost completely
disjunct from both G. maculatus attenuatus and the Lake Rototuna
of 59-64, to a
population, viz. 54-59 (Fig. 2).
The direction of divergence from G. maculatus attenuatus, seen
in the two derivatives, varies; sometimes the counted structures are
fewer in number, as in vertebrae and most of the fin-ray counts
G. macu(Fig. 3). In the case of gill rakers (Fig. 2), in contrast,
latus attenuatus has a total count on the first arch of 13-17, the
Waiparera
fish
15-17. and the Rototuna fish 18-23.
These data
BREVIORA
CBACmS
C.
Jk
11
jL
iiL
Jll
USITATUS
g.
h
4
iL
ATTENUATUS
C
an
No. 265
S
6
7
jlll
ll
13
8
14
ANCHrOSTECALS
1^
16
17
18
19
SO
21
22 23
47 48 49 50
ClLl RAKERS
SI
52 51 54
S5
S6 57
58
59 60
61
62 63 k4
VERTEBRAE
2.
Frequency distribution for counts of branchiostegals, gill rakand vertebrae in Galaxias gracilis, G. maculatiis attenuatiis, and G.
Figure
ers,
usitatus.
DOR5 Al
Figure
fin
3.
f
I
N
RAYS
ANAL FIN RAYS
Frequency distribution for counts of dorsal,
PEL\-1C FIN
anal,
RAYS
and pelvic
rays in Galaxias gracilis, G. maculatiis atteniiatHS, and G. usitatus.
NEW
1967
SPECIES OF GALAXIAS
5
suggest that the meristic distinctions may not be simply a case of
temperature related differences. Differences were also found to
occur in body proportions. In some cases both the derivatives
diverged from G. maculatus attenuatus in the same direction (Fig.
4-2, 4-5), the measured structure being proportionately either
(D
A
B
C
10
9
8
STANDARD LENGTH
©
/
12
11
LENGTH CAUDAL PEDUNCLI
A
B
C
1.8
1.7
2.0
1.9
STANDARD LENGTH
/
2.1
PRE-PELVIC LENGTH
(D
A
B
C
2.6
2.8
3.0
3.2
3.4
3.6
STANDARD LENGTH
®
4.0
3.8
/
PELVIC
-
4.2
4.4
4.6
ANAL LENGTH
A
B
C
9
10
12
II
STANDARD LENGTH
LENGTH DORSAL
/
13
FIN BASE
(D
A
B
C
3.8
4.0
4.2
4.4
4.6
STANDARD LENGTH
©
4.8
/
5.0
5.2
5.4
5.6
3.3
3.4
HEAD LENGTH
A
B
c
2.3
2.4
2.S
2.6
2.7
2.8
HEAD LENGTH
2.9
/
1
3.0
3.1
3.2
3.5
NT E R - ORB IT A L V/IDTH
Figure 4. Ranges for proportional measurements
(A), C. maculatus attenuatus (B), and G. usitatus (C).
in
Galaxies gracilis
BREVIORA
6
No. 265
larger or smaller in both derivatives than in G. maculatus attenuaIn other cases, the divergence has gone in opposite directions,
and the range for G. maculatus attenuatus was found to lie betus.
tween the ranges for the derivative populations (Figs. 4-1, 4-4).
These data indicate that each of the two populations should be
regarded as a full species, distinct from G. maculatus attenuatus
and from each other.
SYSTEMATIC DESCRIPTION
Galaxias gracilis^
Figure 5; Table
n.sp.
la.
Holotype: Deposited in collection of Fisheries Research DiNew Zealand Marine Department.
Paratypes: Dominion Museum, New Zealand. Reg. No. 4499;
vision,
Museum
of Comparative Zoology, Harvard University, No. 45053;
Smithsonian Institution Fish Collection No. USNM 201224.
Type
locality:
Auckland,
Figure
5.
New
Upper Lake Rototuna, Kaipara Harbour, North
Zealand.
Galaxias gracilis n.sp. Length to caudal fork, 59
Description:
A
mm.
small, slender, shoaling species with long head,
low vertebral count and rearward placement of the pelvic
fins.
A
D
fork length 62.5 mm.
i-iii,
i-iii, 7-10; C 16;
12-16; Pel 6-8; Pec 12-14; Branchiostegals 4-6; Vertebrae 47-50;
Gill-rakers 5-7 (upper), 13-17 (lower limb of first arch), total
Maximum known
18-23.
on head, latercylindrical, slender, somewhat depressed
compressed on caudal peduncle, deeper than broad. Caudal
peduncle slender and short. Head small, slender, a little broader
Trunk
ally
than deep, lower jaw protruding a
upper;
1
lips
thin,
Named on
cleft
account of
little,
or equal in length to
extending to a
of
mouth
its
slender form, from the Latin gracilis, slender.
slightly oblique,
NEW
1967
line
file,
SPECIES OF GALAXIAS
through anterior eye margin.
with inter-orbital flat.
Eye
large, at
7
upper head pro-
Mandibular and premaxillary teeth without canines, lingual
teeth strong, entopterygoidal teeth moderately developed; gill-rakers strongly developed; pyloric caeca lacking.
Fins membranous and short, except anal which is long based.
Distal margin of dorsal fin rounded to straight, anterior rays longest.
Anal origin more or less below dorsal origin, distal margin
of fin straight, anterior rays longest, maximum fin length little
longer than base length. Pelvic fins inserted relatively far back,
pelvic-anal interval short, fin relatively short in pelvic-anal length.
Pectoral fin disposed laterally, fin short. Caudal fin forked, fin tips
rounded, depth about equal to body depth.
Coloration: Trunk covered with a dense peppering of large
melanophores, which intensify on the head and dorsum of the
trunk, failing lateroventrally, and ventrally. Fresh material is silver
in these latter areas.
variation: Dorsal rays (segmented), 7(1), 8(21),
10(5); Caudal 15(4), 16(42), 17(4); Anal 12(1),
13(5), 14(30), 15(13), 16(1); Pelvic 6(7), 7(40), 8(3); Pectoral 12(8), 13(28), 14(14); Vertebrae 47(1), 48(16), 49(24),
50(9); Branchiostegals 4(2), 5(27), 6(21); Gill-rakers (total
count) 18(2), 19(3), 20(13), 21(7), 22(3), 23(2).
Differs from G. maculatns attennatus (Jenyns) in having a much
lower vertebral count, fewer dorsal rays, a somewhat lower branchiostegal count and more gill rakers; also in a longer pre-pelvic
length, longer head, narrower inter-orbital, larger eye, short dorsal
fin base, smaller maximum size reached, and the lack of a marine
whitebait juvenile stage. Differs from G. usitatiis n.sp. in having
fewer vertebrae, fewer branchiostegals, a greater number of gill
Meristic
9(23),
rakers, a longer pelvic base-anal origin length, shorter dorsal fin
base, lack of serrations on the opercular membrane and the smaller
maximum size attained.
Galaxias usitatus^
n.sp.
Figure 6; Table lb.
Holotype: Deposited in collection of Fisheries Research DiviNew Zealand Marine Department.
sion,
1
Named on
Latin
iisitatiis,
account of
ordinary.
its
lack of highly distinctive characters,
from the
BREVIORA
8
No. 265
Museum, New Zealand Reg. No. 4500;
Comparative Zoology, Harvard University, No. 45054;
Smithsonian Institution Fish Collection No. USNM 201223.
Paratypes: Dominion
Museum
Figure
Type
of
Galaxias
6.
locality:
iisitatus n.sp.
Length
to caudal fork, 72
Lake Waiparera, North Auckland,
mm.
New
Zealand.
A
slender, lacustrine, shoaling species, similar to
Galaxias maculatus attenuatus, with long head, a short pelvic-anal
interval, with many of the fishes examined having six rather than
Description:
the more usual seven pelvic fin rays. Distinctive in the presence
of fine but definite serrations on the free margin of the opercular
Maximum known fork length 81.5 mm. D i-iii, 9-12;
ii-v, 12-16; Pel 5-7; Pec 11-15; Branchiostegals 5-7;
14-18;
Vertebrae 54-59; Gill-rakers 4-5, 11-13, total 15-17.
membrane.
A
C
Trunk
cylindrical, slender, somewhat depressed on head, latcompressed on caudal peduncle and somewhat deeper than
broad. Caudal peduncle slender and short. Head long and narrow, slender, about as deep as broad; jaws equal, prominent, cleft
slightly oblique reaching to about anterior eye margin, gape rather
narrow. Eye large, placed close to upper head profile, inter-orbital
more or less flat, broad relative to head width. Mandibular and
erally
maxillary teeth without canines, lingual teeth strong, entopterygoidal teeth well developed; pyloric caeca lacking; gill rakers well
developed; free margin of operculum finely serrate.
Fins membranous and short, except anal which is long based.
Dorsal fin set well back, fin with moderately short base, distal
margin of fin somewhat rounded. Anal fin origin more or less
below dorsal origin; anal fin long based but greatest fin length little
greater than base length, distal margin of fin about straight
and inclined to body axis. Pelvic fin inserted at about mid-point
of standard length, pelvic-anal length short, pelvic fin moderate in
pelvic-anal interval, thus short. Pectoral fin base disposed laterally,
fin
fin short. Caudal fin forked, fin
depth about equal
tips rounded,
to
body depth.
NEW
1967
SPECIES OF GALAXIAS
9
Trunk a dusky gray-brown and covered with irregudark blotches similar to G. maculatus attenuatus. When alive,
Coloration:
lar
and ventral abdomen is silvery, in preserved maunpigmented.
Meristic variation: Dorsal rays (segmented) 9(4), 10(28),
11(8), 12(l);Caudal 14(1), 15(4), 16(34), 17(1), 18(1); Anal
12(2), 13(10), 14(13), 15(15), 16(1), Pelvic 6(30), 7(11);
Pectoral 11(1), 12(5), 13(21), 14(12), 15(2); Vertebrae 54(2),
55(5), 56(10), 57(12), 58(9), 59(3); Branchiostegals 5(1),
6(25), 7(15); Gill-rakers 15(2), 16(11), 17(7).
Differs from G. maculatus attenuatus in having a lower vertebral
count, fewer pelvic fin rays, longer head, somewhat larger eye,
shorter pelvice-anal interval; differs from G. gracilis in details discussed under the diagnosis of that species. It differs from both
G. maculatus attenuatus and G. gracilis by the presence of serrathe lateroventral
terial, largely
tions
on the opercular margin.
DISCUSSION
The two new species described above are interpreted as landlocked derivatives of one of the New Zealand sea-going species,
G. maculatus attenuatus. In Lake Okataina, thermal lakes district.
North Island, and in one of the Kaihoka Lakes, near Cape Farewell, there are two land-locked populations of the sea-going G.
fasciatus Gray. The upland-alpine lake species G. koaro Phillipps
and G. lynx Hutton are also envisaged, by the writer, as freshwater derivatives of G. brevipinnis GUnther, a species with marine
stages. It was suggested (McDowall, 1965). that Retropinna abbreviata McDowall and R. lacustris Stokell had speciated under
similar circumstances
in isolation, in lakes cut off from the sea
—
with a migratory population captured in the impounded water
body. Looked at from this perspective, the distribution patterns of
some of the apparently younger species in New Zealand's freshwater fish fauna make greater sense, e.g. G. lynx, present in alpine
lakes
all
along the eastern side of the main divide of the South
Island, to the west of the divide in the
Nelson Lakes
district, with,
according to the arrangement of Stokell (1949) a highly disjunct
population in Lake Waikaremoana, near East Cape in the North
Island. This pattern appears best explained by derivation of the
freshwater lacustrine form, probably several times, from the parent species G. brevipinnis. G. koaro probably has the same mode
of derivation, from G. brevipinnis, one or several times, in the
lakes of the volcanic plateau of the North Island, and further study
may well suggest that G. lynx and G. koaro are conspecific.
BREVIORA
10
No. 265
This view of speciation in the Galaxiidae probably suppHes the
key to understanding much of the fauna, both phylogenetically
and zoogeographically.
ACKNOWLEDGEMENT
The
writer
is
grateful to Dr.
Giles
and for reading the manuscript, and
W. Mead
for his advice
to Messrs. K. F.
Maynard and
W.
Skrzynski for assistance in collecting the specimens. The financial
support of a New Zealand National Research fellowship during the study
is
gratefully acknowledged.
LITERATURE CITED
Cunningham,
1953.
B. T., et al.
A
survey of the western coastal dune lakes of the North Island,
New Zealand. Aust. J. Mar. Freshw. Res. 4 (2): 343-386, 2 pis.
R. M.
new species of Retropinna from Lake Omapere, North Auckland. Rec. Dom. Mus. N.Z. 5 (13): 89-91, 1 fig.
McDowALL,
1965.
1966.
A
Further observations on Galaxias whitebait and their relation to
the distribution of the Galaxiidae. Tuatara 14(1): 12-18, 2
figs.
Pollard, D. A.
1964.
Studies on the reproductive cycle of Galaxias attemiatus.
Soc. Limn. Newslett. 3(1): 10.
Aust.
Stokell, G.
1949.
The systematic arrangement
Specific classification.
10
1964.
A
of the
New
Zealand Galaxiidae.
Trans. Roy. Soc. N.Z.
77
(4):
IL
472-496,
figs.
new
species of Galaxias
Mus. N.Z. 5 (6): 45-48,
(Received 10 October, 1966.)
1
from Victoria,
fig.
Australia.
Rec.
Dom.
NEW
1967
SPECIES OF GALAXIAS
TABLE
Morphometric variation
in
Standard length/Body depth at vent
Standard length/Caudal peduncle length
Caudal peduncle length/Peduncle depth
Pre-dorsal length/Standard length
Standard length/Dorsal fin base length
Dorsal fin length/Fin base length
Standard length/Anal fin base length
Anal fin length/Fin base length
Pre-pelvic length/Standard length
Pectoral-pelvic length/Standard length
Pectoral fin length/Pectoral-pelvic length
Pelvic-anal length/Standard length
Pelvic fin length/Pelvic anal length
Head
length/Inter-orbital width
Head length/Eye diameter
Head length/Gape width
1.
Galaxias gracilis and G. usitatus.
Ratio
Standard length/Head length
Head length/Head width
11
a.
G.
gracilis
8.25-9.50
b.
G. usitatus
BREVIORA
Mmseimm of Comparsitive Zoology
Cambridge, Mass.
Number
6 April, 1967
266
A NEW SPECIES OF VESICOMYA
FROM THE CARIBBEAN SEA
(MOLLUSCA: BIVALVIA: VESICOMYIDAE)
By
Kenneth Jay Boss
Museum
of Comparative Zoology
Harvard University
M
/V OREGON of the
During Cruise 104 (fail 1965) of the
Bureau of Commercial Fisheries Pascagoula Fishery Station. Pascagoula, Mississippi, an unusually large bivalve was trawled, alive,
from a depth of over two hundred fathoms (366 m) off the coast
of Colombia in the Caribbean Sea. Upon examination and comparison with material in the United States National Museum, the
specimen was found to be referable to the rare and enigmatic
family Vesicomyidae. The unique specimen
with any known species of this family and
is
is
not conspecific
herein described
as new.
Vesicomya (Callogonia) caribbea
sp.
nov.
Figures 1-6
Holotype: Division of Mollusks, U.
log
S.
National
Museum,
cata-
number 674573.
^Type locality: M/V OREGON Station 5692, 12 3 1'N; 70 58'W;
205 fathoms (375 m); Caribbean Sea, off Cabo la Vela, Peninsula
de Guajira, Colombia; bottom temperature 55T (12.8°C); 10
October 1965. The specimen was collected alive by a 40' shrimp
=
trawl.
Description:
Shell
96
mm
long,
67
mm
high and 54
mm
wide,
irregularly elliptical, inequilateral, equivalve, solid, frangible, inflated with both valves of equal convexity, without
gape,
posterior
but with slight undulate flexure to right posteriorly. Umbos anterior, conspicuous, involute, pointed, prosocline, slightly elevated
BREVIORA
2
and
No. 266
umbonal
cavity deep. Anterior margin not extensive,
rounded and weakly convex; ventral margin extensive, weakly convex, rising gently posteriorly; anterior dorsal
margin short, semisigmoid, concave umbonally, rounded and convex distally; posterior dorsal margin convexly arcuate and coextensive with posterior margin, forming broad blunt, oblique truncainflated;
very broadly
tion;
outline weakly pointed posteroventrally.
Sculpture closely
concentric laminae, grouped between larger, more conspicuous, irregular growth rings; radial sculpture not evident. Posterior
ridge, semisulcated dorsally, radiating from umbo toward postero-
set, fine
ventral region, becoming weaker distally. Ligament strong, protuberant, black, elongate, lanceolate, slightly inset basally, sup-
ported by thickened hinge line, and forming broad elongate nymph.
Lunule not developed or circumscribed by impressed isocardioform line. Hinge dentition invested with periostracum. Right
valve with two cardinal teeth beneath
umbo; ventral tooth stronger
and protuberant; dorsal tooth with anterior laminar portion and
posterior thickened portion. Left valve with single central cardinal
tooth developed, strong and protuberant; anterior laminate portion
broken and obsolete; secondary laminate tooth beneath
broken.
on
umbo
No
true internal radial rib, but rib-like thickening present
posterodorsal margin of anterior adductor muscle scar. Muscle
moderately impressed, large, irregularly ovate, anterior
smaller than posterior. Pallial line weakly convex; pallial sinus
irregular, narrow; pallial line not directly or obviously contiguous
scars
with posterior adductor muscle scar. Internal surface of valve
Periostracum dehiscent, olivaceous,
wrinkled, heavier peripherally, also thickened over cardinal and
with radial vermiculations.
anterior portions of hinge internally. Shell basically white, externally grayish to olivaceous, discolored centrally with russet
band; earthy and chalky in texture; internally shining, with darkened blotches and pale salmon centrally.
Remarks: The family Vesicomyidae (originally spelled Vesicomyacidae) was established by Dall and Simpson (1901). It
has been reviewed by Lamy ( 1920), and recently Odhner (1960)
has listed the species referable to Vesicomya. The status of the
family has been questioned: Thiele (1935). Odhner (1960)
and Clarke ( 1962) included Vesicomya in the Kellyellidae. JukesBrowne (1913) even mentioned it in relation to the Veneridae.
On
the other hand, Dall (1908), Thiele and Jaeckel (1931),
Prashad (1932), Taki and Habe (1955), and Newell (1965)
have maintained the Vesicomyidae separately.
NEW
1967
SPECIES OF VESICOMYA
3
what genera should be included
For
example, Woodring (1938) placed
Vesicomyidae.
Calyptogena Dall. along with his newly described genera Ectenagena and Phreagena, in the Vesicomyidae. An historical survey
of the family and a critical revision of at least the western Atlantic
There
in
also a question as to
is
the
is
currently being prepared.
western Atlantic Vesicomya approaches the size of V caribbea.
V. leeana (DalK 1889, p. 440; 1890, pi. 10, figs. 6-9)
is the
only western Atlantic species that is closely related to and
which might be confused with V. caribbea. The latter is easily
distinguished by being much larger and having a heavier shell with
species
No
.
a distinct posterior ridge. In addition, the hinged teeth of V. caribbea are stronger and more blunt. The eastern Pacific species. V.
gigas (Dall, r896, pi. 18; 1908, pi. 16, fig. 9), attains the size of
V. caribbea but it is usually less heavily shelled and its teeth are
more distinct. It may be diflferentiated from V. caribbea by its
much
shorter ligament and shorter,
more
distinct,
nymphal
callos-
Further, V. gigas lacks a posterior ridge and is generally of
ity.
longer, narrower proportions. Also, V. gigas is mesially constricted
ventrally while V. caribbea is not.
species most closely related to V. caribbea are known
from
only
widely separated localities and are also rare in collections. The most closely related is Vesico)n\a cliuni described by
Thiele and Jaeckel (1931, p. 244, pi. 4. fig. 100) from VALDIVIA Station 63, 2 N; 8'4.3'E, from a depth of 2492 m in the
Gulf of Guinea, eastern Atlantic Ocean. Unfortunately, the authors did not figure an internal view of the shell and no specimens
of this species were available for comparison. The outline of the
valves of V caribbea and V cliuni are quite similar; however, the
The two
.
.
semisulcated posterior ridge of V. caribbea appears to be a distinguishing character. Further, according to Thiele and JaeckeFs
description, V. chuni is relatively thin shelled, whereas V. caribbea
is
thick shelled.
The other
species closely resembling V. caribbea is from the
Vesicomya winckwortJii, described by Prashad
(1932, p. 153, pi. 5, figs. 7-8) from SIBOGA Station 17, 7°28.5'S;
15'^28'E, in 1060
depth, north of Java, is founded on a single
valve
which,
right
fortunately, was well illustrated externally and
East Indian area.
1
m
V
caribbea is apparently
internally. In contrast to V. winckworthi,
more inflated, its anterior margin more narrowly rounded, and its
.
stronger and thicker.
Vesicomya caribbea is placed in the subgenus Callogonia Dall
1889 (type-species, by monotypy, Callocardia [Vesicomya] leeana
nymph
4
BREVIORA
No. 266
1889), as its pallial sinus is, though indistinct, somewhat
Thiele and Jaeckel (1931) placed V. chuni, the species
Dall
angular.
most closely related
to V. caribbea, in Callogonia.
ACKNOWLEDGMENTS
Mr. Harvey BuUis, Jr., Director of the Bureau of Commercial
Pascagoula Fishery Station made it possible for me
to participate in Cruise 104 of the M/V OREGON and
generously transferred specimens into my care. Drs. J. Rosewater of
the Division of Mollusks of the U. S. National Museum, D. Cohen
of the Bureau of Commercial Fisheries Ichthyological Laboratory, and W. J. Clench and R. D. Turner of the Museum of Comparative Zoology, Harvard University, critically read the manuThe drawings were inked by Mrs. Mildred Carrington. Durscript.
the
ing
preparation of this report the author was on the staff of
the Ichthyological Laboratory, Bureau of Commercial Fisheries,
Fisheries
Washington, D. C.
LITERATURE CITED
Clarke, A. H., Jr.
1962.
Annotated
list
of the world.
and bibliography of the abyssal marine mollusks
Bull. Nat. Mus. Canada, No. 181, 114 pp.
Dall, W. H.
1889.
1890.
1896.
1908
Report on the Mollusca [BLAKE]. Part II. Gastropoda and
Scaphopoda. Bull. Mus. Comp. Zool., 18: 1-492, pis. 1-40.
Preliminary report on the collection of Mollusca and Brachio-
poda obtained in 1887-'88 [ALBATROSS]. Proc. U.S. Natl.
Mus., 12(773): 219-362, pis. 5-14.
Diagnoses of new species of mollusks from the west coast of
America. Proc. U.S. Natl. Mus., 18(1034): 7-20.
The Mollusca and Brachiopoda [ALBATROSS]. Bull. Mus.
Comp.
Zool..
43(6): 205-487.
pis. 1-22.
Dall. W. H. and C. T. Simpson
1901.
The Mollusca of Porto Rico.
351-524.
Jukes-Browne, A.
1913.
On
Bull.
U.S. Fish
Comm., 20(1):
pis. 53-58.
J.
Collistu, Amiuntis,
and
Pitaria.
Proc. Malac. Soc. London,
10: 335-347.
Lamy,
E.
1920.
Revision des Cypricardiacea
de Conch., 64: 259-307.
et
des Isocardiacea vivants.
Jour.
NEW
1967
SPECIES OF VESICOMYA
5
Newell, N. D.
Classification of the Bivalvia.
1965.
25 pp.,
Amer. Mus.
Novit.,
No. 2206,
3 text figs.
Odhner, N. H.
Mollusca. Kept. Swed. Deep-Sea Exped., 2(Zool. 22): 365-400,
2 pis., 12 text figs.
1960.
Prashad, B.
1932.
The LamelHbranchia
Part,
11
Pelecypoda
Expeditie,
of the SIBOGA Expedition. Systematic
(exclusive of the Pectinidae). SIBOGA-
Monographie 53
c,
353 pp., 9
pis.
and T. Habe
Taki, I.,
1955.
[In]
Kuroda,
6, text-figs.
Thiele,
T.,
Cat. Jap. Shells, 2(1):
J.
1935.
Handbuch der systematischen Weichtierkunde.
Fischer, vol. 2, pp. 779-1022, 110
Thiele.
Illus.
Vesicomyidae.
1-4.
J.,
1931.
and S. Jaeckel
Muscheln der
deutschen
Jena,
Gustav
figs.
Wiss Ergeb.
Tiefsee-Expedition.
161-268 (1-110), pis. 6-10
Deutsch. Tiefsee Exped., 21(1):
(1-5).
WOODRING, W. P.
Lower Pliocene mollusks and echinoids from
1938.
Basin, California.
190, 67
pp., 9 pis.
(Received 20 October, 1966.)
the
Los Angeles
U.S. Dept. Interior, Geol. Surv. Prof. Papers,