Species Description:
P. lethostigma is one member of a large family of distinctive benthic
flatfishes that inhabit continental shore waters in the tropical and temperate
zones of the Atlantic, Pacific and Indian oceans. Flatfishes such as the
flounders are unlike most other fishes in that they begin life as bilateral animals, having equal right and left sides, and swim as do other fishes.
However, toward the end of the larval period, flatfishes settle to the benthos
and take up a cryptic, somewhat sedentary lifestyle, lying on one side of the
body, and swimming laterally to the substratum. Metamorphosis to the juvenile
stage involves complex modification of the skeletal structure of the head, and
rearrangement of the nervous system and muscle tissues. Additionally, the eye on
the side which faces the substratum (termed the blind-side eye) begins to
migrate to the upper side of the body. P. lethostigma is a left-eye
flounder, thus it lies on its right side, and at metamorphosis, the right eye
migrates to the left side of the head. Lefteye flounders sometimes exhibit
sexual dimorphism, with females having eyes that are closer together than in
males, and males having somewhat longer pectoral fins (Rogers and Van Den Avyle
1983).
Body color is light to dark brown with diffuse non-ocellated dark spots and
blotches. The blindside is white or dusky. P. lethostigma are
characterized by the following meristic (number of structures per body part)
counts:
| Character |
Count |
| Dorsal fin Rays: |
80-95 |
| Anal Rays: |
63-74 |
| Pectoral Fin Rays: |
11-13 |
| Upper Gill Rakers: |
2-3 (Upper Limb) |
| Lower Gill Rakers: |
8-11 (Lower Limb) |
| Lateral Line Scales: |
85-100 |
| Body Depth: |
30-47% SL |
Synonymy:
None
Other Taxonomic Groupings:
Subphylum: Vertebrata
Superclass: Osteichthyes
Subclass: Neopterygii
Infraclass: Teleostei
Superorder: Acanthopterygii
Suborder: Pleuronectoidei
Potentially Misidentified Species:
Paralichthys lethostigma is sometimes
confused with P. albigutta, the gulf flounder. The two are easily
distinguished based on the much smaller size of the gulf flounder, which grows
only to 15 inches (38 cm). Additionally, the gulf flounder has 3 ocellated
spots: 2 vertically placed posterior to the pectoral fins, and 1 placed inside
the base of the tail.
II. HABITAT AND
DISTRIBUTION
Regional Occurrence :
The southern flounder, Paralichthys lethostigma, occurs from North
Carolina south through Florida and the Gulf of Mexico to Texas.
IRL Distribution:
The southern flounder occurs throughout the Indian River Lagoon.
III. LIFE HISTORY AND POPULATION BIOLOGY
Age, Size, Lifespan:
Southern flounder attain a size of up to 3
feet (91 cm) in length, and can weigh as much as 9 kg (24.1 lbs.) (Smith et
al. 1999). The von Bertalanffy growth model predicts a maximum age for summer
flounder of approximately of 20 years (Reagan and Wingo 1985).
Abundance:
P. lethostigma is one of the largest
and most commercially valuable flounders in the western North Atlantic (Burke
et al. 1991).
Reproduction:
Adults migrate to offshore spawning grounds
during late fall and winter, though some remain in estuaries year-round.
Spawning migrations are usually preceded by a drop in water temperature of
4 - 5 ° C. Males move
seaward earlier than females, with few remaining in estuaries after November
(Reagan and Wingo 1985). In North Carolina, southern flounders begin migration
in the fall; in Texas, they migrate from October through December (Reagan and
Wingo 1985).
Laboratory experiments from Texas indicate that
approximately 3 weeks before spawning takes place, male southern flounder
begin following gravid females. In tank experiments, the first spawning was in
December and occurred at midday. Females swam to the surface and released eggs
that were immediately fertilized by attending males. Fertilization was 30% to
50% successful, and 6% to 35% of the eggs hatched within 61 - 76 hr (Reagan
and Wingo 1985).
Females become sexually mature at 2 years of age in
Texas, while the youngest mature female southern flounder in northern Florida
was 4 years old (Reagan and Wingo 1985).
Thirteen southern flounders examined in the
laboratory, produced a total of 120,000 eggs (approximately 9,230 eggs per
female) (Reagan and Wingo 1985).
Embryology:
Eggs of P. lethostigma range from 0.85
- 0.95 mm in diameter (Powell and Henley 1995), with a single oil globule.
Laboratory rearing of southern flounder shows that eggs hatch after 3 days at
18° C and 30‰ salinity (Denson and
Smith 1997). Larvae begin to feed when 4 -6 days old, and show signs of
becoming premetamorphic by day 14. By day 16, larvae begin to settle out of
the water column and congregate on the bottom. By day 21, larvae show signs of
adult pigmentation, and begin to rest on their left sides, though their eyes
remain in position. By day 23, metamorphosis is initiated and the left eye
begins to migrate to the right side. Most animals had completed metamorphosis
by day 36 (Denson and Smith 1997). In culture experiments, yolk-sac larvae
began metamorphosing to postlarvae at 40 - 46 days, when they were
approximately 8 - 11 mm in length. Metamorphosis to the
juvenile stage was complete by 50 - 51 days (Reagan and Wingo 1985). Data from
Powell and Henley (1995) show that larvae complete metamorphosis when they
reach approximately 8.7 - 9.0 mm SL. By this time, the migrating eye has
reached the dorsal midline, and the larval stage is complete.
Powell and Henley (1995) examined egg and larval
development in both P. lethostigma and P. albigutta. Results
from their study show that fins begin to develop when larvae reach
approximately 5.4 mm notochord length (NL). The dorsal fin is generally the
first to begin development, followed by the caudal, anal, pelvic, and pectoral
fins (Powell and Henley 1995). Development of the caudal fin in P.
lethostigma can begin when larvae are approximately 5.5 mm NL, but fin
rays are not observed until larvae attain 8.2 mm SL. Dorsal fins begin to
develop when larvae are in the preflexion stage, at approximately 6.5 mm NL.
The dorsal fin is first observed in the head region, with development
proceeding posteriorly. By the time larvae reach 8.4 mm standard length (SL)
the dorsal fin is fully developed. Following postflexion, when larvae reach
approximately 7.3 mm standard length (SL), anal fin rays begin to develop,
with the full adult complement of fin rays reached at a body size of 8.4 mm
SL. Pelvic fins are first observed on larvae at approximately 8.2 mm SL, and
are fully developed by the time larvae attain 9.7 mm SL. Pectoral fins first
begin formation when larvae are approximately 8.4 mm SL, and are fully formed
when larvae exceed 11.0 mm SL.
Pigmentation is first observed in middle-stage eggs,
following blastopore closure. In larvae, pigmentation is more pronounced in
the caudal area, being less developed overall in P. lethostigma than in
its close relative P. albigutta, the gulf flounder (Powell and Henley
1995).
Larvae spawned offshore in the Atlantic Ocean make
their return to estuarine habitats by passive transport on nearshore and tidal
currents from November through April, with a peak in recruitment occurring in
February (Burke et al. 1991). In the gulf of Mexico, Southern flounder
postlarvae are caught along the Gulf of Mexico coast during winter and early
spring. At Galveston Island, Texas, southern flounder postlarvae
18 - 34 mm in total length (TL) were captured during February,
March, and May. Fish 25 - 51 mm TL were caught in the Mississippi River during
the spring. In Aransas Bay, Texas, the peak movement of postlarvae flounders
into estuaries is in February, when water temperature is 16.0 - 16.2 °C (Stokes 1977).
IV. PHYSICAL TOLERANCES
Temperature:
Temperature influences the migration of
postlarval and adult southern flounders (Reagan and Wingo 1985). In Louisiana
coastal waters, adult southern flounders have been collected at temperatures
ranging from 5 - 35 °C.
Salinity:
Southern flounder are highly euryhaline,
and withstand fluctuations in salinities ranging from 0- 35 ‰ or more. Data
from Smith et al. (1999) indicates that salinity tolerance in this species
increases with age.
Adult P. lethostigma make extensive migrations
from estuarine habitats in order to spawn in offshore waters. Eggs of P.
lethostigma are buoyant at 32 ‰, and sink at 29‰, though data indicate
that eggs that sink may still hatch. Experiments conducted by Smith et al.
(1999) showed that eggs incubated in water with a salinity between 0-5 ‰ all
died within a day. Eggs incubated at 10 ‰ had greater hatching success
(82%), but all larvae moved sluggishly and died shortly after hatching. Eggs
incubated in water of salinities between 15 - 35 ‰ were normal in appearance
and were active. However, larvae reared through metamorphosis to the juvenile
stage showed greater mortality at 15‰ salinity than at either 25‰ or 35‰.
Further, recently metamorphosed juveniles showed less tolerance to freshwater
conditions than did older fish (Smith et al. 1999).
Southern flounder eggs and larvae from wild
populations develop in offshore waters, with late stage, premetamorphic larvae
(stage 4b - 5), likely returned to estuarine habitats via passive transport on
nearshore and tidal currents. Once returned to estuaries, larvae settle on the
substratum and metamorphose into juveniles. In one North Carolina study,
comparative data from Burke et al. (1991) suggests that settlement in P.
lethostigma is influenced by salinity. These authors reported that though
larvae of both summer and southern flounder begin to recruit into estuaries
during February, southern flounder larvae concentrated on tidal flats near the
heads of estuaries where salinity ranged from 9 - 25‰, and the substratum
had a low sand content (4 - 50%). Conversely, summer flounder larvae settled
more downstream, in the middle reaches of estuaries where salinity ranged from
24 - 35 ‰ and the substratum had a much higher sand content (53 - 95 %).
Burke et al. (1991) also reported that juvenile
southern flounder moved further upstream to more riverine environments later
in the spring, while juvenile summer flounder tended to remain in higher
salinity tidal areas near Spartina saltmarshes. Catch comparisons
showed that approximately equal numbers of southern flounder were caught in
sandy versus muddy substrate types in low salinity waters; while summer
flounder were most abundant in sandy substrata in higher salinity waters.
Burke et al. (1991) concluded that southern flounder settlement is more highly
correlated with salinity, while summer flounder settlement is more highly
correlated with substratum type.
Other Physical Tolerances:
Dissolved Oxygen:
P. lethostigma
tolerates low dissolved oxygen concentrations (less than 5
mg/l). However, in a
laboratory study, postlarval southern flounder attempted
avoidance when dissolved
oxygen concentrations in culture vessels fell
below
3.7 mg/l (Reagan and Wingo 1985).
V. COMMUNITY ECOLOGY
Trophic Mode:
Southern flounder are carnivorous fishes that
are generally considered to be top or near-top predators. Larvae reared under
laboratory conditions begin feeding on rotifers 4 - 6 days posthatch. By 8 -
13 days posthatch, larvae begin to feed on newly hatched Artemia
nauplii (Denson and Smith 1997).
Small southern flounders consume a wide variety of
invertebrate prey, but upon reaching approximately 20 mm total length (TL),
they become primarily piscivorous (Reagan and Wingo 1985). Based on
differences in morphology and behavior between summer flounder and southern
flounder in North Carolina, Burke (1995) compared prey distribution and
feeding ecology between the 2 species following metamorphosis to the juvenile
stage. Southern flounder juveniles have generally larger mouths, larger,
inwardly curved teeth, and fewer, heavier gill rakers than do summer flounder.
They also tend to remain still on the bottom, waiting for prey to come within
striking distance (Minello et al. 1987; Burke 1995). Small southern flounder
primarily consumed amphipods and mysid shrimp, followed by copepods, insects,
fish and invertebrate parts. In this study, summer flounder 20 - 60 mm SL
consumed spionid polychaete worms, followed by clam siphons, mysid shrimp,
calanoid copepods, the blue crab, Callinectes sapidus, and small
fishes. From this data, Burke (1995) concluded that post-settlement
differences in feeding habits developed between the 2 species, with southern
flounder shifting to more mobile prey which could be attacked from below, and
summer flounder continuing to feed upon benthic prey organisms.
The adult diet of P. lethostigma consists
primarily of fish, but is augmented by crustaceans depending upon regional
location. In Louisiana, adult southern flounders eat shrimp and fish; though,
Fox and White (1969) reported that the primary prey species for southern
flounder was striped mullet (Mugil cephalus). Also included in the diet
are fat sleepers (Dormitator maculatus) and anchovies (Anchoa spp.).
Larger flounders (150 mm long) ate primarily anchovies, menhaden (Brevoortia
spp.), sciaenids, and mullet (Reagan and Wingo 1985).
Habitats:
Adult P. lethostigma spend the warmer
months in coastal embayments and riverine habitats in the upper reaches of
estuaries (Rogers and Van Den Avyle 1983). Many adults migrate to offshore
spawning grounds during late fall and winter, though some do remain in
estuaries year-round. Larvae spawned offshore make their return to estuarine
habitats by passive transport on nearshore and tidal currents. In a study
conducted in North Carolina, Burke et al. (1991) reported that peak
recruitment into estuaries by late stage (stage 4b and 5), premetamorphic
larvae occurred in February, though larvae were collected from late November
through mid-April. These larvae settled into tidal mudflats near the head of
the estuary, however, in spring, southern flounder apparently migrated
upstream into riverine habitats. Spring through summer, southern flounder
prefer the silt and mud substrata of coastal bays and river systems, and
become most common in the upper reaches of estuaries, sometimes entering
freshwater (Burke et al. 1991; Smith et al. 1999).
In a comparative study, Burke et al. (1991) reported
that larvae of both southern and summer flounder recruit into estuaries during
the same period, and for a time, show considerable overlap in distribution
within an estuary. However, segregation occurs quickly (Burke et al. 1991;
Burke 1995). Premetamorphic larvae of southern flounder tend to concentrate on
tidal flats in the upper reaches of estuaries where salinity ranges from 9 -
25 ‰, and the substratum consists of 4 - 45 % sand. Conversely,
premetamorphic larvae from summer flounder generally move into silt and
mudflat areas in the lower and middle reaches of estuaries where salinity
ranges from 24 - 35 ‰ and the substratum consists of 50 - 95 % sand (Burke
et al. 1991). Capture data following segregation of the 2 species within the
Newport River Estuary, North Carolina, showed that summer flounder were most
common on sand flats than on mudflats in the lower estuary, while there was
little difference in capture rates among southern flounder in sandy vs. muddy
substrates in the upper reaches of the estuary. Burke et al. (1991) concluded
that settlement in P. dentatus is most likely influenced by substratum
type, while that of P. lethostigma is influenced by salinity.
Activity Time:
A tank study showed that southern flounder
tend to be more active at night than during the day (Reagan and Wingo 1985).
VI. SPECIAL STATUS
Special Status:
Fisheries.
Fisheries Importance:
The southern flounder is a valuable sport and
commercial fish along the Gulf coast of the United States. Most of the commercial catch in the Gulf
of Mexico is incidental to the catch by shrimp trawlers. There has been
significant interest in utilizing southern flounder as an aquaculture species.
Studies in the southeastern U.S. and in the Gulf of Mexico are currently
underway to improve spawning techniques and develop larval rearing methods for
southern flounder in order to improve its attractiveness as an aquaculture
product (Jenkins and Smith 1999; Smith et al. 1999).
Flounders of all species are harvested annually from
waters in and around the Indian River Lagoon, and are especially prized by recreational
anglers. However, the commercial fishery is not of particularly high value.
For the years 1987 - 2001, 1.7 million pounds of flounders were harvested, with
a dollar value of over $3.1 million reported in the 5 county area encompassing
the IRL (Volusia, Brevard, Indian River, St. Lucie and Martin Counties).
This ranks flounders nineteenth in commercial value within the IRL, and
twenty-ninth in pounds harvested.
Figure 1 below shows the dollar value of the flounder
fishery to IRL counties by year. Note that all species of flounders were
combined in the data presented. As shown, commercial catch ranged from a low of $77,149 in
1987 to a high of over $350,927 in 1999. Volusia County annually accounts
for the largest percentage of the flounder catch with 83% in total (Figure 2),
followed distantly by Brevard County, which accounts for 8% of the total.
Indian River, St. Lucie and Martin Counties account for 3%, 4% and 2% of the
total respectively. Note that the fishery's value brings in $125,000 -
$300,000 annually to Volusia County businesses, while in all other IRL counties,
the dollar value is typically less than $25,000.

Figure 1. Annual dollar value of
the commercial catch of flounders to the 5-county area
of the Indian River
Lagoon.

Figure 2. Breakdown of total
flounder
dollar value by county for the years 1987 - 2001.
|
|
Volusia |
Brevard |
Indian River |
St. Lucie |
Martin |
Total |
| |
Value |
Value |
Value |
Value |
Value |
Value |
|
YEAR |
($) |
($) |
($) |
($) |
($) |
to IRL |
|
1987 |
$52,332 |
$16,478 |
$462 |
$4,740 |
$3,137 |
$77,149 |
|
1988 |
$125,679 |
$24,502 |
$773 |
$4,896 |
$6,499 |
$162,349 |
|
1989 |
$159,271 |
$0 |
$0 |
$5,312 |
$0 |
$164,583 |
|
1990 |
$135,210 |
$20,461 |
$1,113 |
$10,947 |
$5,396 |
$173,127 |
|
1991 |
$168,724 |
$20,692 |
$2,446 |
$22,654 |
$6,410 |
$220,926 |
|
1992 |
$117,085 |
$16,988 |
$2,813 |
$15,816 |
$4,620 |
$157,322 |
|
1993 |
$182,403 |
$20,647 |
$1,574 |
$11,826 |
$7,469 |
$223,919 |
|
1994 |
$202,828 |
$15,739 |
$6,091 |
$5,041 |
$5,984 |
$235,683 |
|
1995 |
$238,435 |
$14,654 |
$6,773 |
$5,227 |
$4,412 |
$269,501 |
|
1996 |
$137,805 |
$7,207 |
$7,347 |
$638 |
$2,625 |
$155,622 |
|
1997 |
$194,655 |
$20,528 |
$19,640 |
$7,254 |
$2,787 |
$244,864 |
|
1998 |
$145,311 |
$16,449 |
$13,133 |
$14,215 |
$5,855 |
$194,963 |
|
1999 |
$306,281 |
$25,090 |
$9,182 |
$8,772 |
$1,602 |
$350,927 |
|
2000 |
$265,389 |
$19,629 |
$3,097 |
$13,248 |
$3,244 |
$304,607 |
|
2001 |
$148,233 |
$14,655 |
$9,103 |
$4,789 |
$1,256 |
$178,036 |
|
Cumulative
Totals: |
$2,579,641 |
$253,719 |
$83,547 |
$135,375 |
$61,296 |
$3,113,578 |
Table 1. Total dollar value of
flounders to IRL counties between
1987 -2001.
|
|
Volusia |
Brevard |
Indian River |
St.
Lucie |
Martin |
| |
% |
% |
% |
% |
% |
|
YEAR |
Total |
Total |
Total |
Total |
Total |
|
1987 |
67.8% |
21.4% |
0.6% |
6.1% |
4.1% |
|
1988 |
77.4% |
15.1% |
0.5% |
3.0% |
4.0% |
|
1989 |
96.8% |
0.0% |
0.0% |
3.2% |
0.0% |
|
1990 |
78.1% |
11.8% |
0.6% |
6.3% |
3.1% |
|
1991 |
76.4% |
9.4% |
1.1% |
10.3% |
2.9% |
|
1992 |
74.4% |
10.8% |
1.8% |
10.1% |
2.9% |
|
1993 |
81.5% |
9.2% |
0.7% |
5.3% |
3.3% |
|
1994 |
86.1% |
6.7% |
2.6% |
2.1% |
2.5% |
|
1995 |
88.5% |
5.4% |
2.5% |
1.9% |
1.6% |
|
1996 |
88.6% |
4.6% |
4.7% |
0.4% |
1.7% |
|
1997 |
79.5% |
8.4% |
8.0% |
3.0% |
1.1% |
|
1998 |
74.5% |
8.4% |
6.7% |
7.3% |
3.0% |
|
1999 |
87.3% |
7.1% |
| |