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Mosquito
control impoundments are areas of salt marsh or mangrove forest that have been
diked to allow control of water levels for purposes of mosquito control. Within
the dikes, perimeter ditches are flooded artificially in order to control
breeding and reproduction of salt marsh mosquitoes without the use of
pesticides. Florida’s mangroves and salt marshes have historically been problem
areas in one important respect: they are preferred breeding habitat for salt
marsh mosquitoes (Ochlerotatus taeniorrhynchus and O. sollicitans).
These mosquitoes are an important nuisance species that affect the health of
humans and domestic animals. Salt marsh mosquitoes do not reproduce by laying
their eggs in standing water. Rather, they deposit eggs in the moist soils of
high marsh above the water line in tidal wetlands (Provost 1976). Eggs will
remain dormant, often for long periods of time, until water levels rise in
response to rains or tides. Eggs hatch in the water and undergo several larval
stages before developing into adult mosquitoes within 5 days. In the vicinity
of the Indian River Lagoon, concerted efforts aimed at controlling salt marsh
mosquitoes began in the mid-1920s (Platt et al. 1943) with construction
of miles of hand-dug, parallel ditches. These efforts were not highly
successful because of the heavy maintenance required to maintain the ditches,
and because tidal effects in the ditched areas were generally of such low
amplitude that little mosquito control was effected (Rey and Rutledge 2001).
In
the 1930’s field experiments demonstrated that controlling water levels through
impoundment would provide source reduction of mosquito populations by
effectively controlling mosquito reproduction (Hull and Dove 1939). However,
this experimental program was abandoned as water losses within the impoundment
through seepage and evaporation became problematic. Attention then turned
toward the use of pesticides such as DDT. However, by the 1950s, concerns over
pesticide resistance in insects began to emerge, and the focus of mosquito
control again shifted back to source reduction.
The
first impoundments in Florida were built in Brevard County in 1954, with other
counties soon following. By the 1970’s, in excess of 40,000 acres of Florida’s
coastal wetlands had been impounded (Rey and Kain 1990). The majority of
impoundments were constructed at the mean high water level and then flooded year
round, closed off from adjacent estuarine waters. Some, however, were allowed
to drain during the winter months, but were flooded again as mosquito breeding
season approached.
Negative effects of closed impoundments:
Although impoundment for mosquito control is an effective method of controlling
mosquito populations, there are often severe environmental impacts on impounded
wetlands isolated from adjacent estuaries. Particularly important are issues of
water quality degradation, isolation of important fishery species from critical
nursery habitats, interruption of nutrient flow between wetlands and estuarine
waters, creation of unnaturally high water levels, and hypersaline conditions
that may develop in closed impoundments when evaporation of water occurs. Any
negative changes in any of these physical parameters may lead to the elimination
of vegetation from such areas (Rey and Rutledge 2001).
Water levels:
Excessively high water levels brought on by overflooding impoundments eliminated
some species from salt marsh and mangrove communities altogether. While only a
thin film of water is enough to prevent oviposition by salt marsh mosquitoes;
impoundments are typically flooded to depths of 15 – 50 cm above the surface to
compensate for evaporation effects (Rey et al. 1991). In closed
impoundments, this practice eliminated some species such as saltwort (Batis
maritima), and glasswort (Salicornia bigelovii, and Salicornia
virginica), and also impacted black mangroves due to their short
pneumatophores not being able to withstand prolonged flooding (Rey and Rutledge
2001).
Water quality:
Closed impoundments showed significant changes in both water quality and soil
chemistry. In many areas, isolation of flooded impoundments resulted in
decreased dissolved oxygen concentrations and increases in both nitrogen and
sulfide concentrations in soils. Some impoundments flooded by use of artesian
wells showed ecological turnovers from having communities composed of
predominantly halophytic species, to communities characteristic of fresh water
habitats. Other impoundments were subject to hypersaline conditions when
estuarine waters were pumped in to flood them during warm summer months.
Because these impoundments were closed to adjacent waters, lack of flushing and
evaporation resulted in extremely high salinities, which caused local
extinctions of some species (Rey and Rutlege 2001).
Effects on fish and invertebrates:
Fish species were greatly affected by closed impoundments, with numbers of
some species being significantly reduced in species that utilized salt marsh or
mangrove areas as nursery grounds (Harrington and Harrington 1961, Snelson 1976,
Gilmore et al. 1982, Rey et al 1990). Tarpon (Megalops atlanticus),
ladyfish (Elops saurus), common snook (Centropomus undecimalis),
mullet (Mugil cephalus), and other species important to commercial and
recreation fisheries were adversely impacted by closed impoundments. Marine
invertebrates were also impacted by isolation of impounded wetlands, with
biodiversity and species abundance changing dramatically in some areas. In some
areas, the invertebrate community became more characteristic of freshwater
wetlands than marine or estuarine wetlands (Brockmeyer et al. 1997).
Nutrient flow:
In closed impoundments, natural patterns of nutrient flow are interrupted
between mangrove areas and adjacent waters. In unaltered systems, nutrients
from mangrove leaf fall, which are decomposed into particulate and dissolved
forms, are utilized in a variety of ways by many different organisms as
mangroves are flushed by tides. In closed impoundments, however, nutrients are
never flushed from mangrove areas because there is no connection to estuarine
waters, and thus remain confined within impoundments.
Improved Impoundment Strategies:
An improved strategy for impoundments was experimented with as early as the
mid-1960s. This involved seasonal flooding of impoundments during peak mosquito
breeding season. For the remainder of the year, impoundments were opened via
culverts penetrating the dike so that water levels within the impoundment could
fluctuate naturally with tides. In 1974, seasonal impoundment was combined with
active water management. This strategy of allowing for impoundments to be
adequately flushed by tides not only controlled salt marsh mosquitoes, but also
helped to retain black mangroves and other vegetation, and allowed the return of
juvenile fishes to nursery areas unavailable to them in closed impoundments.
This management strategy is currently referred to as Rotational Impoundment
Management (RIM).
Under
RIM, estuaries retain many of their natural functions, and their primary
productivity can rival that of unaltered wetlands (Lahmann 1998, Rey et al.
1990b). Culverts remain open between the impoundment and the estuary from
October to May to allow water exchange and use of impoundments by transient fish
species and invertebrates. Then, during the summer months, culverts are closed
and impoundments flooded to the minimum levels needed to prevent oviposition in
salt marsh mosquitoes. Low areas of the surrounding dike, called spillways,
insure that water levels do not exceed prescribed levels, thus preventing injury
to vegetation. RIM has proven to be an effective strategy for controlling
mosquitoes while minimizing serious environmental impacts to estuaries. Data
from Rey et al. (1991) shows that RIM is currently the most commonly
employed management strategy in 3 of the 5-counties adjacent to the Indian River
Lagoon. St. Lucie County has 1,371 hectares (ha) (3386.4 acres) of wetlands
under RIM, Brevard County has 1,037 ha (2561.4 acres), and Indian River County
has 448 ha (1106.5 acres).
Select a highlighted link below to learn more about
that species:
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Species Name: |
Common Name: |
Habitat Useage: |
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Mangrove Plants: |
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Acrostichum danaeifolium |
Mangrove fern |
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Avicennia germinans |
Black
mangrove |
Upper
intertidal |
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Batis maritima |
Saltwart |
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Borrichia frutescens |
Sea
Ox-eye |
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Casuarina equistifolia |
Australian pine |
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Conocarpus erecta |
Buttonwood, Button mangrove |
High
intertidal, scrub |
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Halodule beaudettei |
Shoalgrass |
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Halophila decipiens |
Paddlegrass |
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Halophila englemanni |
Star
grass |
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Halophila johnsonii |
Johnson’s seagrass |
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Juncus roemerianus |
Black
needlerush |
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Laguncularia racemosa |
White
mangrove |
Higher
intertidal |
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Limonium carolinianum |
Sea
lavender |
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Melaleuca quinquenervia |
Melaleuca |
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Monarda punctata |
Spotted
beebalm |
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Rhizophora mangle |
Red
mangrove |
Lower
and middle intertidal |
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Ruppia maritima |
Widgeon
grass |
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Salicornia bigelovii |
Annual
glasswart |
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Salicornia virginica |
Perennial glasswart |
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Schinus terebinthifolia |
Brazilian pepper |
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Suaeda linearis |
Sea
blite |
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Sueda maritima |
Sea
blite |
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Syringodium filiforme |
Manatee
grass |
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Thalassia testudinium |
Turtlegrass |
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Verbesina virginica |
White
crownbeard, frostweed |
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Mangrove Algae, Diatoms, and Other Protists: |
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Acanthophora spicifera |
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Anacystis montana |
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Anadyomena sp. |
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Caulerpa sertularoides |
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Caulerpa spp. |
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Chaetoceros spp. |
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Chaetomorpha linum |
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Cladophoropsis membranacea |
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Cryptoperidinopsis spp. |
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Derbesia vaucheriaeformis |
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Enteromorpha spp. |
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Gonyaulax monilata |
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Gracilaria spp. |
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Gymnodidium pulchellum |
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Halimeda discoidea |
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Hypnea spp.. |
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Lyngbya lutea |
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Nitzchia spp. |
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Paralia spp. |
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Phorinidium crosbyanum |
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Polysiphonia sp. |
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Scrippsiella subsalsa |
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Skeletonema costatum |
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Spirulina sp. |
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Sturea anastomosans |
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Thalssiosira spp. |
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Ulva
spp. |
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Mangrove animals: |
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Abudefduf saxatilus |
Sergeant major |
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Acetes americanus |
Aviu
shrimp |
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Achirus lineatus |
Lined
sole |
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Acteocina canaliculata |
Cahnneled barrel-bubble |
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Aiptasia pallida |
Pale
anemone |
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Ajaia ajaia |
Roseate
spoonbill |
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Alligator mississipensis |
American alligator |
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Alpheus armillatus |
Banded
snapping shrimp |
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Alpheus heterochaelis |
Common
snapping shrimp |
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Amygdalum papyrum |
Atlantic papermussel |
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Anachis semiplicata |
Gulf
dovesnail |
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Anas
acuta |
Northern pintail |
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Anas
americana |
American widgeon |
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Anas
clypeata |
Northern shoveler |
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Anas
crecca |
Green-winged teal |
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Anas
discors |
blue-winged teals |
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Anas
fulvigula |
Mottled
duck |
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Anas
spp. |
Dabbling ducks |
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Anchoa cubana |
Cuban
anchovy |
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Anchoa hepsetus |
Striped
anchovy |
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Anchoa lyolepis |
Dusky
anchovy |
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Anchoa mitchelli |
Bay
anchovy |
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Anguilla rostrata |
American eel |
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Anhinga anhinga |
Anhinga |
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Anomalocardia auberiana |
Pointed
venus |
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Apalone ferox |
Florida
softshelled turtle |
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Arca
imbricata |
Mossy
ark |
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Aratus pisoni |
Mangrove crab |
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Archosargus probatocephalus |
Sheepshead |
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Archosargus rhomboidalis |
Sea
bream |
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Arctia tonsa |
Calanoid copepod |
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Ardea alba |
Great
egret |
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Ardea herodias |
Great
blue heron |
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Arius felis |
Hardhead catfish |
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Ascidia curvata |
Curved
tunicate |
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Ascidia nigra |
Black
tunicate |
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Assiminea spp. |
(none) |
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Astyris lunata |
Lunar
dovesnail |
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Atherinomorus stipes |
Hardhead silverside |
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Aythya affinis |
Lesser
scaup |
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Aythya americana |
Redhead
duck |
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Aythya collaris |
Ringneck duck |
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Aythya valisineria |
Canvasback |
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Bagre marinus |
Gafftopsail catfish |
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Balanus eburneus |
Ivory
barnacle |
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Bairdiella chrysoura |
Silver
perch, yellowtail |
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Bathygobius curacao |
Notchtongue goby |
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Bathygobius soporator |
Frillfin goby |
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Bittiolum varium |
grass
cerith |
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Boonea impressa |
Impressed odostome |
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Botryllus planus |
Variable encrusting tunicate |
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Brachidontes exustus |
Scorched mussel |
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Branchiomma nigromaculata |
Black
spotted fanworm |
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Brevoortia smithi |
menhaden |
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Brevoortia tyrannus |
Atlantic menhaden |
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Bubulcus ibis |
Cattle
egret |
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Bucephala albeola |
Bufflehead |
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Bulla striata |
Striate
bubble |
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Bunodosoma cavernata |
American warty anemone |
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Bunodosoma graniliferum |
Red
warty anemone |
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Bursatella leachii pleii |
Browsing sea hares |
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Busycon contrarium |
Lightning whelk |
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Butroides virescens |
Green
backed heron |
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Calidris alpina |
Dunlin |
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Calidris mauri |
Western
sandpiper |
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Calidris minutilla |
Least
sandpiper |
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Calidris spp. |
Sandpipers |
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Callinectes bocourti |
Red
crab |
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Callinectes ornatus |
ornate
blue crab |
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Callinectes sapidus |
blue
crab |
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Callinectes similis |
lesser
blue crab |
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Capitella spp. |
Polychaete worm |
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Caranx hippos |
Crevalle jack |
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Carcharhinus leucas |
bull
shark |
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Cardinalis cardinalis |
Cardinal |
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Cardisoma guanhumi |
giant
land crab |
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Carditamera floridana |
Broad
ribbed carditid |
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Cassiopeia frondosa |
Upside-down jellyfish |
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Cassiopeia xamachana |
Upside-down jellyfish |
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Catoptrophorus semipalmatus |
Willet |
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Centropomus parallelus |
Fat
snook |
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Centropomus pectinatus |
Tarpon
snook |
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Centropomus undecimalis |
common
snook |
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Centropristis philadelphica |
Rock
sea bass |
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Ceratozona squalida |
Eastern
surf chiton |
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Cerithidea scalariformis |
Ladderhorn snail |
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Cerithium muscarum |
Flyspeck cerith |
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Chaetodipterus faber |
Atlantic spadefish |
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Charadrius vociferus |
Killdeer |
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Charadrius semipalmatus |
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