Esox americanus
redfin pickerel
Type Locality
Esox americanus,
vicinity of New York City (Gmelin 1788).
Etymology/Derivation of Scientific Name
Esox, an old European
word for pike; americanus, “from America” (Ross 2001).
Synonymy
Esox lucius americanus
Gmelin1788:1390 in Mettee et al. 1987
Esox americanus Cook
1959:72.
Esox americanus
vermiculatus Lesueur 1846 in Cuvier and Valenciennes 1846:335
Esox
umbrosus Hay 1883:67
Esox
vermiculatus Cook 1959:72
Characters
Maximum size: 381 mm
TL (Ross 2001).
Life colors: Adult
pattern first appears at about 130-140 mm in length. Dorsal surface and
upper sides uniform pale to dark green, there is a rusty brown mid-dorsal
stripe, the sides show 15-23 olive to black, thin, wavy, vertical bars
separated by lightly pigmented extensions of what had in the young been a
prominent golden green lateral band. Pale area between adjacent bars is
wider than the bars. Ventral, vertical, suborbital and horizontal,
preorbital, black bars obvious, sometimes postorbital, horizontal bar
obvious; lateral edges of both jaws lightly pigmented; the pupil is yellow;
the leading edge of all fins is black, the rest of the fins dusky to amber
(Scott and Crossman 1973). Young grass pickerel have an unpigmented lateral
band that extends from the snout to the base of the caudal fin. In addition,
they have a silvery green, middorsal band that extends from the tail to the
tip of the snout (Crossman 1962).
Counts: 11-13
branchiostegal rays; fewer than 115 scale rows along body (Hubbs et al.
1991); 17-21 dorsal rays; 16-20 anal rays (Crossman 1966); 13-17 pectoral
rays; 8-10 pelvic rays (Ross 2001).
Body shape: Long,
cylindrical, somewhat flat dorsally, shallow, greatest depth (between paired
fins) is 12.1-17.4% of TL, cross section almost round; snout short (into
head length 2.4-2.7; Becker 1983), rounded and concave on top, only
moderately broad; eyes high, moderately large (Scott and Crossman 1973).
Mouth position:
Terminal (Goldstein and Simon 1999); large canine teeth in lower jaw
flattened to rear (Becker 1983).
External morphology:
Opercles with scales covering most of ventral half (Hubbs et al. 1991); top
of head unscaled; cheek scaled; gill rakers reduced to sharp, toothlike
structures; scales cycloid; principal dorsal fin rays, principal anal fin
rays, pectoral fin rays, pelvic fin rays all rounded on edge; caudal fin
forked (Becker 1983).
Distribution (Native and Introduced)
U.S. distribution:
Inhabits Coastal Plain from MA to south NH, Lac St. Pierre (St. Lawrence
River) region of Quebec, Canada, south in Hudson River to coastal NY, from
east PA south to St. Mary’s River system in GA. Waters from southwestern GA,
south to Lake Okeechobee, FL, and the Gulf of Mexico systems from Suwanee
River, FL and GA, to Biloxi River, MS. Pearl River, LA, west to Brazos
River, TX, north through eastern OK, southeastern MO, east border of IA, to
southwestern WI. East across southern MI and southern Ontario, Canada to
tributaries of southwestern shore of Lake Ontario and those of Niagra River,
western NY, including tributaries of Lake Ontario, some of the Finger Lakes
and those of St. Lawrence, in Ontario, Canada and NY, as far downstream as
mouths of Ottawa and Chateauguay rivers in Quebec, Canada. Eastern limit
runs southwest from NY, west of mountains along line from northwestern PA to
central MS, including Tennessee River in Northwestern AL (Crossman 1980).
Texas distribution:
Primarily restricted to the eastern part of the state and coastal streams
from the Red River Basin south to the Brazos River Basin (Hubbs et al.
1991). Warren et al. (2000) list the Red River drainage unit for
distribution of this species in the state.
Abundance/Conservation status (Federal, State, NGO)
Not listed as threatened or
endangered by Texas Parks and Wildlife Department
(2006). Populations in the
southern United States are currently secure (Warren et al. 2000).
Habitat Associations
Macrohabitat: Streams,
drainage canals, ponds, and bays of small lakes (Crossman 1980).
Mesohabitat: Small,
quiet, heavily vegetated waters (Crossman 1980). Common in waters with
neutral or slightly basic pH and sandy or rocky substrata (Crossman 1966;
1980). In Lamar Co., Mississippi, E. americanus occurs in habitat
characterized by high amounts of aquatic vegetation and cover, fine
substrata such as mud and silt, high litter amounts, and water depths of
over 0.5 m (Ross et al. 1987). Evans and Noble (1979) noted a high relative
abundance of Esox americanus, the single largely piscivorous species
collected, in the headwaters of Big Sandy Creek, Texas where the streambed
is mostly clay, with some silt and sand, and large, impervious clay
substrate pools are found; these pools helping to negate the impact of
drought in headwater areas.
Biology
Spawning season:
Spring spawner, but also reported to spawn in fall with water; the two
periods probably coinciding with water temperatures of about 10°C (Crossman 1980; Crossman 1966; Kleinert and Mraz 1966).
Spawning habitat: In
flood plains, E. americanus spawns along grassy margins, or in other
areas of heavy vegetation (Ross and Baker 1983; Kwak 1988). Phytophils;
obligatory plant spawners with adhesive egg envelopes that stick to
submerged dead or live plants (Kleinert and Mraz 1966; Simon 1999).
Reproductive strategy:
No nest, parental care, or defense of territory (Crossman 1980; Simon 1999).
Open substratum spawner (Simon 1999). Eggs are broadcast and abandoned,
settling and adhering to vegetation (Becker 1983).
Fecundity: Moderately
large number of small demersal, adhesive eggs (Crossman 1980). Mature eggs
average 1.9mm in diameter and are golden yellow; range from 843 to 4584
mature eggs for grass pickerel of 160-325 mm TL (Kleinert and Mraz 1966).
Age at maturation:
Sexually mature by at least age two, at 134-174 mm TL (Crossman 1980).
Migration: In spring
adults proceed upstream and on to flooded stream margins or marshes were
vegetation is plentiful. It is probable that changing water temperature and
an increase in temperature stimulate spawning (Scott and Crossman 1973).
Longevity: 7-8 years
(Scott and Crossman 1973; Crossman 1980).
Growth: Hatchlings 6.2
mm long (Scott and Crossman 1973; Becker 1983). In Wisconsin, early growth
in different years appears to be similar and rapid; 6.5-11.5 mm TL on 24
April, 10-17 mm on 9 May, 25-29 mm on 25 May, 31-49 mm on June 3. Scale
analysis of a combined sample of 280 pickerel from six Wisconsin lakes
indicates average lengths at different ages as: age 0 - 145 mm; I – 208 mm;
II – 251 mm; III - 287 mm; IV – 356 mm. Females are longer than males at age
0, I, and II; no males of age III were encountered, indicating females
exceed males in growth and longevity (Kleinert and Mraz 1966).
Food habits:
Invertivore/carnivore; benthic predator and drift/whole body feeder; trophic
mode: lie-in-wait/ambush. Intestine long and undifferentiated (Goldstein and
Simon 1999). Food of very young grass pickerel (to 50 mm TL) is cladocerans,
amphipods, osterocods, isopods, and immature or adult insects from the
orders Diptera, Plecoptera, and Hemiptera. In the size range 50-100 mm they
begin to prey on fishes, but diet is mainly Trichoptera, Odonata, and
crayfish. Beyond 100 mm diet is almost exclusively fish and crayfish;
dragonfly nymphs form part of the food of even the largest individuals
(Scott and Crossman 1973; Goldstein and Simon 1999). In a Wisconsin study,
fishes found in fingerling stomachs include lake chubsuckers and smaller
pickerels; in stomachs of grass pickerel 152-343 mm TL, small bluegills were
one of the two predominant fishes consumed (Kleinert and Mraz 1966). In an
Ontario, Canada creek, 22 species of fish were present, but grass pickerel
fed on only 9 species (of which include the following species found in
Texas, in descending order of importance): golden shiner, grass pickerel,
creek chub, and yellow perch (Crossman 1962b).
Phylogeny and morphologically similar fishes
Hybridizes in nature with
E. niger (chain pickerel; Crossman 1980). Most similar to E. niger,
from which it can be readily separated from as an adult on the basis of
color pattern: irregular vertical bars compared to the reticulate or honey
combed pattern markings on the flank of the chain pickerel (Ross 2001).
Host Records
Trematoda: Posthodiplostomum minimum; Nematoda:
Agamonema (Arnold et al 1967). Contracaecum (Mayberry 2000).
Protzoa: Trichodina renicola; Trematoda: Azygia angusticauda,
Crassiphiala bulbglossa, Macroderoides flavus; Cestoda:
Proteocephalus ambloplitis, P. pinguis; Nematoda: Spiruridae
(Hoffman 1967).
Commercial or Environmental
Importance
As this
species is associated with heavily vegetated areas and deeper pools, it is
sensitive to raparian damage from livestock or to any erosional problems
resulting in increased sedimentation, bank failure, and loss of vegetation
(Ross 2001). Populations negatively affected where streams are channelized
and denuded of vegetation and where swamps have been drained (Boschung and
Mayden 2004). E. americanus eaten by catfishes, sunfishes, yellow
perch, and redfin pickerel themselves (Becker 1983).
[Additional literature
noting collection of this species from Texas locations includes, but is not
limited to the following: Hubbs (1957); Village Creek (Hardin Co.;
Moriarty and Winemiller 1997).]
References
Arnold, J.G., Jr., Ph.D., H.E. Schafer, M.S., R.L.
Vulliet, BSMT.1967. The parasites of the freshwater fishes of
Louisiana.
Becker, G.C. 1983.
Fishes of Wisconsin. University of Wisconsin, Madison. 1052 pp.
Boschung, H.T.,
Jr., and R.L. Mayden. 2004. Fishes of Alabama. Smithsonian Books,
Washington. 736 pp.
Cook, F.A. 1959.
Freshwater fishes in Mississippi. Mississippi Game and Fish Commission,
Jackson.
Crossman, E.J.
1962. The redfin pickerel Esox a. americanus in North Carolina.
Copeia 1962(1):114-123.
Crossman, E.J.
1962b. Predator-prey relationships in pikes (Esocidae). J. Fish. Res. Board
Canada 19(5):979-980.
Crossman, E.J.
1966. A taxonomic study of Esox americanus and its subspecies in
eastern North America. Copeia 1966(1):1-20.
Crossman, E.J.
1980. Esox americanus (Gmelin), Redfin Pickerel and Grass
Pickerel.pp.131 in D.S. Lee et al. Atlas of North American Freshwater
Fishes. N.C. State Mus. Nat. Hist., Raleigh, i-r+854 pp.
Cuvier, G. and Valenciennes [1846] 1969. Histoire naturelle des poisons.
Vol. 19. A. Asher and Co., Amsterdam. 544 pp.
Evans, J.W., and
R.L. Noble. 1979. The longitudinal distribution of fishes in an east Texas
stream. American Midland Naturalist 101(2):333-343.
Gmelin. 1788. Systema naturae,
Laurentii Salvii, Holmiae, 13 ed.
Goldstein, R.M.,
and T.P. Simon. 1999. Toward a united definition of guild structure for
feeding ecology of North American freshwater fishes. pp. 123-202 in
T.P. Simon, editor. Assessing the sustainability and biological integrity of
water resources using fish communities. CRC Press, Boca Raton, Florida.
Hay, O.P. 1883. On a collection of fishes from the lower Mississippi
Valley. Bull. U.S. Fish Comm. 2:57-75.
Hoffman G.L. 1967.
Parasites of North American Freshwater Fishes. University of California
Press. Berkeley and Los Angeles, CA 1-486.
Hubbs, C. 1957.
Distributional patterns of Texas fresh-water fishes. The Southwestern
Naturalist 2(2/3):89-104.
Hubbs, C., R.J.
Edwards and G.P. Garret. 1991. An annotated checklist of freshwater fishes
of Texas, with key to identification of species. Texas Journal of Science,
Supplement 43(4):1-56
Kleinert, S.J. and
Mraz. 1966. Life history of the grass pickerel (Esox americanus
vermiculatus) in southeastern Wisconsin. pp.1-40. Tech. Bull., no. 37,
Wisconsin Conservation Department, Madison.
Kwak, T.J. 1988.
Lateral movement and use of floodplain habitat by fishes of the Kankakee
River, Illinois. Amer. Midl. Nat. 120(2):241-249.
Mayberry, L.F.,
A.G. Canaris, J.R. Bristol, and S.L. Gardner. 2000. Bibliography of parasite
and vetebrate hosts in Arizona, New Mexico, and Texas (1893-1984).
University of Nebraska Harold W. Manter Laboratory of Parisitology Web
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Mettee, M.F., P.E. O’Neil, R.D. Suttkus, and J.M Pierson. 1987. Fishes of
the lower Tombigbee River system in Alabama and Mississippi. Geol. Surv.
Ala. Bull. 107:1-186.
Moriarty, L.J.,
and K.O. Winemiller. 1997. Spatial and temporal variation in fish assemblage
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southeastern stream. Amer. Midl. Nat. 109(1):1-14.
Ross, S.T., J.A.
Baker, and K.E. Clark. 1987. Microhabitat partitioning of southeastern
stream fishes: temporal and spatial predictability, pp. 42-51. In:
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Mathews and D.C. Heins, eds. Univ. Oklahoma Press, Norman.
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Research Board of Canada, Ottawa. 966 pp.
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North American Freshwater Fishes, pp. 97-121. In: Simon, T.L. (ed.).
Assessing the sustainability and biological integrity of water resources
using fish communities. CRC Press. Boca Raton, Florida. 671 pp.
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online at: http://gis.tpwd.state.tx.us/TpwEndangeredSpecies/DesktopModules/AcountyCodeKeyForWebESDatabases.pdf
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