Strongylura marina
Atlantic needlefish
Type Locality
Long Island, NY (Walbaum
1792).
Etymology/Derivation of Scientific Name
Strongylura, from
Greek strongylos, meaning “round, circular” and oura, meaning
“tail,” apparently referring to the round cross section of the body;
marina, from Latin marinus, meaning “of the sea,” from mare,
meaning “the sea” (Boschung and Mayden 2004).
Synonymy
Esox marinus Walbum
1792:88.
Strongylura marina
Cook 1959:36.
Characters
Maximum size: 640 mm
SL (Burgess 1980).
Coloration: Back, head
and snout are dark green, grading to silvery on the sides and white on the
undersides. Bright, silvery white midlateral band, and a dark predorsal
band. Anal and pelvic fins are immaculate to dusky; pectoral and dorsal fins
lightly pigmented. Caudal fin heavily pigmented, usually bluish near base.
Small specimens may have scattered melanophores below the silvery white band
on the sides, and fins may be unpigmented (Ross 2001).
Counts: Approximately
325 lateral line scales (Hildebrand and Schroeder 1928); 14-17 dorsal rays;
15-20 anal rays; 10-11 pectoral rays; 6 pelvic rays (Ross 2001).
Body shape: Slender,
cylindrical, not compressed (Hardy 1978). Snout needle-shaped (Hubbs et al.
1991); jaws about twice as long as rest of head; teeth in bands in jaws,
sharply pointed, the innermost enlarged and canine-like (Hardy 1978).
External morphology:
Lateral line low (Hubbs et al. 1991); scales cycloid, small and thin
(Boschung and Mayden 2004); large eyes; truncate or slightly forked caudal
fin; dorsal and anal fins are small, and are set very far back on the body;
pectoral fins inserted high on the body; pelvic fins set far back on body;
gill rakers absent (Ross 2001); the dorsal insertion is located behind the
anal fin origin (Foster 1974). Ross (2001) notes that both upper and lower
jaws of larvae are initially equal in length; however, lower jaw begins to
grow more rapidly than the upper jaw, so that the upper jaw does not again
equal length of the lower jaw until late in the juvenile stage.
Distribution (Native and Introduced)
U.S. distribution:
This estuarine species inhabits coastal waters from Maine to Brazil; may
also be found considerable distances upstream in the lower portions of
coastal streams (Hubbs et al 1991).
Texas distribution:
Warren et al. (2000) listed the following drainage units for distribution of
Strongylura marina in the state: Sabine Lake (including minor coastal
drainages west to Galveston Bay), Galveston Bay (including minor coastal
drainages west to mouth of Brazos River), Brazos River, Colorado River, San
Antonio Bay (including minor coastal drainages west of mouth of Colorado
River to mouth of Nueces River), Nueces River.
Abundance/Conservation status (Federal, State, NGO)
Populations in southern drainages are currently stable
(Warren et al. 2000).
Habitat Associations
Macrohabitat:
Estuarine (Hubbs et al. 1991). Only North American belonid that commonly
enters fresh water. Moves upstream as far as the Fall Line (Burgess 1980).
Reported from coastal ponds, large springs, and canals (Hardy 1978).
Mesohabitat: Adults
found primarily inshore, in shallow water, usually at the surface. Maximum
salinity, 36.9 ppt (Hardy 1978).
Biology
Spawning season: Late
spring and early summer, in the Potomac River (Foster 1974). In Texas, near
ripe females reported in mid-February (Hardy 1978).
Spawning Habitat:
Occurring in fresh and brackish water in shallows with submerged algal
masses (Hellier 1967; Foster 1974).
Spawning behavior: The
eggs are demersal, adhesive, and attached via filaments to algal mats
(Breder and Rosen 1966; Foster 1974; Hardy 1978).
Fecundity: Fertilized
eggs large, spherical, averaging 3.5-3.6 mm diameter. Eggs have numerous,
uniformly spaced filaments about equal to egg diameter in length (Breder and
Rosen 1966; Foster 1974; Hardy 1978; Ross 2001). Only the ovary on the right
side of the body is developed (Collette 1968).
Age at maturation:
Probably in 2nd year (Hardy 1978).
Migration: Apparently
makes definite seasonal inshore-offshore movements (Hardy 1978).
Growth and Population
structure: Newly hatched larvae relatively large at 9.2-14.4 mm TL
(Foster 1974; Hardy 1978).
Longevity:
Food habits: Diet
includes various small fishes, copepods, mysids, shrimp, and insects
(Hildebrand and Schroeder 1928; Darnell 1958; Springer and Woodburn 1960;
Carr and Adams 1973). Larger fish primarily
piscivorous, manipulating prey into a headfirst position by moving their own
body around the prey, which remains motionless in the water due to inertia.
Changes in food habits occur as a result of the growth in length of
the upper jaw relative to the lower, early juveniles being at a stage where
the upper jaw is much shorter than the lower jaw (Boughton et al. 1991). At
this stage fish feed mainly on planktonic invertebrates including
amphipods, mysids, and small shrimps, switching almost exclusively to fish
prey at 50 mm SL (Carr and Adams 1973) when upper jaw length is at least 60%
of lower jaw length (Boughton et al. 1991).
Phylogeny and morphologically similar fishes
It is most likely to be
confused with gars or pickerels (originally placed in genus Esox by
Walbaum in 1792). Species can be distinguished from gars by the truncate or
forked, homocercal caudal fin (as opposed to abbreviate heterocercal) caudal
fin and by thin, flexible cycloid scales (as opposed to heavy, ganoid
scales). Can be separated from the pickerels and other freshwater fishes by
narrow and elongated jaws; pectoral fin base high on the body; and
elongated, slender body (Ross 2001).
Host Records
Trematoda: Bucephaliodes strongylurae, Rhipidocotyle transversale
(Mayberry et
al. 2000).
Commercial or Environmental
Importance
References
Boschung, H. T., Jr., and R. L. Mayden. 2004. Fishes of Alabama. Smithsonian
Books, Washington. 736 pp.
Boughton, D. A., B. B. Collette, and A. R. McCune. 1991. Heterochrony in jaw
morphology of needlefishes (Telostei: Belonidae). Syst. Zool. 40(3):329-354.
Breder, C.M., Jr., and D.E. Rosen. 1966. Modes of Reproduction in Fishes.
T.F.H. Publications, Jersey City, N.J. 941 pp.
Burgess, G. H. 1980. Strongylura marina (Walbaum), Atlantic
needlefish. P. 489 in D.S. Lee, et al. Atlas of North American
Freshwater Fishes. N. C. State Mus. Nat. Hist., Raleigh, i-r+854 pp.
Carr, W. E. S., and C. A. Adams. 1973. Food habits of juvenile marine fishes
occupying seagrass beds in the estuarine zone near Crystal River, Florida.
Trans. Amer. Fish. Soc. 102(3):511-540.
Collette, B.B. 1968. Strongylura timucu (Walbaum): a valid species of
western Atlantic needlefish. Copeia 1968(1):189-192.
Cook, F.A. 1959. Freshwater Fishes of Mississippi. Mississippi Game and Fish
Commission, Jackson. 239 pp.
Darnell, R. M. 1958. Food habits of fishes and larger invertebrates of Lake
Pontchartrain, Louisiana, an estuarine community. Univ. Texas, Publ. Inst.
Mar. Sci. 5:353-416.
Foster, N. R. 1974. Strongylura marina-Atlantic Needlefish, pp.
125-126 In: Manual for identification of early developmental stages
of fishes of the Potomac River estuary. A. J. Lippson and R. L. Moran, eds.
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for the freshwater fishes of Texas, with keys to identification of species.
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Mississippi, Jackson. 624 pp.
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of the Tampa Bay area. Prof. Pap., ser. no. I, Florida State Board of
Conservation, St. Petersburg. 104 pp.
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pars III. J. Cramer, Wheldon and Whesley, Ltd., Codicote, Herts.
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and W. C. Starnes. 2000. Diversity, distribution and conservation status of
the native freshwater fishes of the southern United States. Fisheries
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