MOSQUITO IMPOUNDMENTS

 

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:
 

Species Name:

Common Name:

Habitat Useage:

Mangrove Plants:

 

 

Acrostichum danaeifolium

Mangrove fern

 

Avicennia germinans

Black mangrove

Upper intertidal

Batis maritima

Saltwart

 

Borrichia frutescens

Sea Ox-eye

 

Casuarina equistifolia

Australian pine

 

Conocarpus erecta

Buttonwood, Button mangrove

High intertidal, scrub

Halodule beaudettei

Shoalgrass

 

Halophila decipiens

Paddlegrass

 

Halophila englemanni

Star grass

 

Halophila johnsonii

Johnson’s seagrass

 

Juncus roemerianus

Black needlerush

 

Laguncularia racemosa

White mangrove

Higher intertidal

Limonium carolinianum

Sea lavender

 

Melaleuca quinquenervia

Melaleuca

 

Monarda punctata

Spotted beebalm

 

Rhizophora mangle

Red mangrove

Lower and middle intertidal

Ruppia maritima

Widgeon grass

 

Salicornia bigelovii

Annual glasswart

 

Salicornia virginica

Perennial glasswart

 

Schinus terebinthifolia

Brazilian pepper

 

Suaeda linearis

Sea blite

 

Sueda maritima

Sea blite

 

Syringodium filiforme

Manatee grass

 

Thalassia testudinium

Turtlegrass

 

Verbesina virginica

White crownbeard, frostweed

 

Mangrove Algae, Diatoms, and Other Protists:

 

 

Acanthophora spicifera

 

 

Anacystis montana

 

 

Anadyomena sp.

 

 

Caulerpa sertularoides

 

 

Caulerpa spp.

 

 

Chaetoceros spp.

 

 

Chaetomorpha linum

 

 

Cladophoropsis membranacea

 

 

Cryptoperidinopsis spp.

 

 

Derbesia vaucheriaeformis

 

 

Enteromorpha spp.

 

 

Gonyaulax monilata

 

 

Gracilaria spp.

 

 

Gymnodidium pulchellum

 

 

Halimeda discoidea

 

 

Hypnea spp..

 

 

Lyngbya lutea

 

 

Nitzchia spp.

 

 

Paralia spp.

 

 

Phorinidium crosbyanum

 

 

Polysiphonia sp.

 

 

Scrippsiella subsalsa

 

 

Skeletonema costatum

 

 

Spirulina sp.

 

 

Sturea anastomosans

 

 

Thalssiosira spp.

 

 

Ulva spp.

 

 

Mangrove animals:

 

 

Abudefduf saxatilus

Sergeant major

 

Acetes americanus

Aviu shrimp

 

Achirus lineatus

Lined sole

 

Acteocina canaliculata

Cahnneled barrel-bubble

 

Aiptasia pallida

Pale anemone

 

Ajaia ajaia

Roseate spoonbill

 

Alligator mississipensis

American alligator

 

Alpheus armillatus

Banded snapping shrimp

 

Alpheus heterochaelis

Common snapping shrimp

 

Amygdalum papyrum

Atlantic papermussel

 

Anachis semiplicata

Gulf dovesnail

 

Anas acuta

Northern pintail

 

Anas americana

American widgeon

 

Anas clypeata

Northern shoveler

 

Anas crecca

Green-winged teal

 

Anas discors

blue-winged teals

 

Anas fulvigula

Mottled duck

 

Anas spp.

Dabbling ducks

 

Anchoa cubana

Cuban anchovy

 

Anchoa hepsetus

Striped anchovy

 

Anchoa lyolepis

Dusky anchovy

 

Anchoa mitchelli

Bay anchovy

 

Anguilla rostrata

American eel

 

Anhinga anhinga

Anhinga

 

Anomalocardia auberiana

Pointed venus

 

Apalone ferox

Florida softshelled turtle

 

Arca imbricata

Mossy ark

 

Aratus pisoni

Mangrove crab

 

Archosargus probatocephalus

Sheepshead

 

Archosargus rhomboidalis

Sea bream

 

Arctia tonsa

Calanoid copepod

 

Ardea alba

Great egret

 

Ardea herodias

Great blue heron

 

Arius felis

Hardhead catfish

 

Ascidia curvata

Curved tunicate

 

Ascidia nigra

Black tunicate

 

Assiminea spp.

(none)

 

Astyris lunata

Lunar dovesnail

 

Atherinomorus stipes

Hardhead silverside

 

Aythya affinis

Lesser scaup

 

Aythya americana

Redhead duck

 

Aythya collaris

Ringneck duck

 

Aythya valisineria

Canvasback

 

Bagre marinus

Gafftopsail catfish

 

Balanus eburneus

Ivory barnacle

 

Bairdiella chrysoura

Silver perch, yellowtail

 

Bathygobius curacao

Notchtongue goby

 

Bathygobius soporator

Frillfin goby

 

Bittiolum varium

grass cerith

 

Boonea impressa

Impressed odostome

 

Botryllus planus

Variable encrusting tunicate

 

Brachidontes exustus

Scorched mussel

 

Branchiomma nigromaculata

Black spotted fanworm

 

Brevoortia smithi

menhaden

 

Brevoortia tyrannus

Atlantic menhaden

 

Bubulcus ibis

Cattle egret

 

Bucephala albeola

Bufflehead

 

Bulla striata

Striate bubble

 

Bunodosoma cavernata

American warty anemone

 

Bunodosoma graniliferum

Red warty anemone

 

Bursatella leachii pleii

Browsing sea hares

 

Busycon contrarium

Lightning whelk

 

Butroides virescens

Green backed heron

 

Calidris alpina

Dunlin

 

Calidris mauri

Western sandpiper

 

Calidris minutilla

Least sandpiper

 

Calidris spp.

Sandpipers

 

Callinectes bocourti

Red crab

 

Callinectes ornatus

ornate blue crab

 

Callinectes sapidus

blue crab

 

Callinectes similis

lesser blue crab

 

Capitella spp.

Polychaete worm

 

Caranx hippos

Crevalle jack

 

Carcharhinus leucas

bull shark

 

Cardinalis cardinalis

Cardinal

 

Cardisoma guanhumi

giant land crab

 

Carditamera floridana

Broad ribbed carditid

 

Cassiopeia frondosa

Upside-down jellyfish

 

Cassiopeia xamachana

Upside-down jellyfish

 

Catoptrophorus semipalmatus

Willet

 

Centropomus parallelus

Fat snook

 

Centropomus pectinatus

Tarpon snook

 

Centropomus undecimalis

common snook

 

Centropristis philadelphica

Rock sea bass

 

Ceratozona squalida

Eastern surf chiton

 

Cerithidea scalariformis

Ladderhorn snail

 

Cerithium muscarum

Flyspeck cerith

 

Chaetodipterus faber

Atlantic spadefish

 

Charadrius vociferus

Killdeer

 

Charadrius semipalmatus