Survival of Larvivorous Fish Used for Biological Control of Aedes aegypti Larvae in Domestic Containers With Different Chlorine Concentrations

2009 ◽  
Vol 46 (4) ◽  
pp. 841-844 ◽  
Author(s):  
Luciano Pamplona de Góes Cavalcanti ◽  
Francisco José de Paula ◽  
Ricardo José Soares Pontes ◽  
Jorg Heukelbach ◽  
José Wellington de Oliveira Lima
2016 ◽  
Vol 48 (2) ◽  
pp. 137
Author(s):  
Soujita Pramanik ◽  
Sampa Banerjee ◽  
Soumyajit Banerjee ◽  
Goutam K. Saha ◽  
Gautam Aditya

Among the natural predators, larval stages of the mosquito <em>Lutzia fuscana (</em>Wiedemann, 1820) (Diptera: Culicidae) bear potential as a biological control agent of mosquitoes. An estimation of the predatory potential of the larva of <em>L. fuscana</em> against the larva of the dengue vector <em>Aedes aegypti</em> (Linnaeus, 1762) (Diptera: Culicidae) was made to highlight its use in vector management. Laboratory experiments revealed that the larva of<em> L</em>. <em>fuscana</em> consumes 19 to 24 <em>A. aegypti</em> larvae per day, during its tenure as IV instar larva. The consumption of <em>A. aegypti</em> larvae was proportionate to the body length (BL) and body weight (BW) of the predatory larva<em> L. fuscana</em> as depicted through the logistic regressions: y = 1 / (1 + exp(-(-2.09 + 0.35*BL))) and y = 1 / (1 + exp(-(0.4+ 0.06*BW))). While the prey consumption remained comparable among the days, the net weight gained by the <em>L</em>. <em>fuscana</em> larva showed a decreasing trend with the age. On the basis of the results, it is apparent that the larva of the mosquito <em>L. fuscana</em> can be used in the regulation of the mosquito <em>A. aegypti</em> through augmentative release, particularly, in the smaller mosquito larval habitats.


1951 ◽  
Vol 42 (2) ◽  
pp. 355-370 ◽  
Author(s):  
J. Muspratt

Living specimens of Megarhinus brevipalpis were transported from southern Natal to Johannesburg to establish an insectary-bred colony. The natural habitat of these predatory mosquitos consisted of small isolated patches of sub-tropical forest, in which the rainfall is 40–50 ins. (102–127 cm.) with a mean winter temperature of 64°F. (17·7°C.) and an annual range of 27°–33°F. (15°–18°C). The breeding places were leaf axils of Strelitzia nicolai (a plant resembling a wild banana), small rot holes in trees and larger ones in Strelitzia stumps. The larvae were collected from leaf axils with an apparatus consisting of a rubber bulb to which were attached lengths of glass and rubber tubing.The insectary was a room 9 ft.×8 ft. 6 ins. and 9 ft. high which was kept at tropical heat and humidity. Mating of the adults was observed, copulation being effected while at rest or in flight. Oviposition was usually accomplished in flight but also while at rest on the surface of the water. In the summer time two females, which were tested, laid about 85 eggs each during the month following emergence from the pupa, six or seven days elapsing after emergence before the first oviposition. In the middle of the winter, oviposition (with later generations) became very irregular in spite of the temperature and humidity remaining constant. The adults, which were comparable to those of the natural habitat, were fed on sugar solution, honey and fruit juice. One bred out as a gynandromorph.When given an abundant supply of larvae of laboratory bred Aëdes aegypti, the life-cycle of M. brevipalpis was normally : egg (incubation), less than two days ; larva, 11–20 days (average 14·5 days) ; pupa, five days. This does not include a small number of exceptional cases in which the life as a fully grown larva was abnormally prolonged (in one case nearly four months) for reasons which are not absolutely clear. The larvae killed from 100 to 200 or more Aëdes larvae during the normal larval life, but many of these were not eaten when the brevipalpis were in the late fourth instar. By a special technique they were also induced to eat dead tissues including minced pork brawn, minced maggots and minced flies. Except for the latter these were not satisfactory foods although there was slow development.Fourth-instar larvae were kept out of water for three to four weeks (without food), in a damp atmosphere, and afterwards when fed most of them developed normally, but pupation was sometimes suspended for a considerable time. They have been sent by post (out of water) in tubes with damp cotton wool and filter paper.The egg differed from that of other Megarhinus species in having a crown of projections at one end with a cup-like structure in the centre. The exochorion had roughly hexagonal cells but without numerous tubercles as in other species.First-instar larvae remained in the egg-shell after hatching when the eggs-were out of water but on a damp surface and in a saturated atmosphere. They survived like this for up to six days or about the same time as the larvae survived in tap water if there was no food. When liberated in water the head of the first-instar larva was comparatively small with the mouth parts folded in. Within two hours of liberation in water the head enlarged considerably and the mouth parts came into position ; the larva was then ready to catch its Culicine prey. When in water containing dead leaves, these larvae survived from a few days to over four weeks and some grew to the third instar without any Culicine food.Cannibalism was investigated. Fourth-instar larvae did not attack each other readily ; they devoured smaller larvae of their own species and small to medium size larvae resorted to cannibalism, particularly in the absence of Culicine prey. There was evidence that fourth-instar Aëdes aegypti occasionally ate first-instar Megarhinus.The discussion traces attempts which have been made in certain Pacific islands, notably Hawaii and Fiji, to use Megarhines for biological control of disease-carrying mosquitos. M. brevipalpis has a shorter life-cycle than the species introduced into these islands and the conclusion reached is that laboratory breeding, to enable large numbers to be released in certain areas, would be a suitable adjunct to a programme of general control, in this part of the world. Airmail consignments of larvae are being sent to Hawaii with the object of starting a laboratory colony there.


2008 ◽  
Vol 16 (04) ◽  
pp. 565-577 ◽  
Author(s):  
CLAUDIA PIO FERREIRA ◽  
HYUN MO YANG ◽  
LOURDES ESTEVA

The efficacy of biological control of Aedes aegypti mosquitoes using Sterile Insect Technique (SIT) is analyzed. This approach has shown to be very efficient on agricultural plagues and has become an alternative control strategy to the usual technique of insecticide application, which promotes resistance against chemical controls and is harmful to other species that live in the same mosquito habitat. By using a discrete cellular automata approach we have shown that in the case of Aedes aegypti, the spatially heterogeneous distribution of oviposition containers and the mosquito behavior, especially with respect to mating, make the application of STI difficult or impracticable.


2017 ◽  
Author(s):  
Ricardo M. Souza Ricardo M. Souza

2017 ◽  
Vol 2 (3) ◽  
pp. 91-96 ◽  
Author(s):  
Willian Marinho Dourado Coelho ◽  
Juliana de Carvalho Apolinário Coêlho ◽  
Katia Denise Saraiva Bresciani ◽  
Wilma Aparecida Starke Buzetti

2012 ◽  
Vol 72 (2) ◽  
pp. 243-247 ◽  
Author(s):  
EB. Campanini ◽  
CC. Davolos ◽  
ECC. Alves ◽  
MVF. Lemos

The entomophatogenic bacterium Bacillus thuringiensis produces crystal proteins, named Cry proteins which are encoded by the cry genes. This bacterium is used on biological control of important economical pests, as well as in the control of disease´s vectors, such as Aedes aegypti, a mosquito that transmits the dengue viruses. Isolates of this bacterium can be characterized by the content of cry genes and this prediction helps target different insect orders. In this research, we isolated 76 colonies of B. thuringiensis from 30 soil samples that were taken from Ilha Bela (SP, Brazil), a place where simulids are already biologically controlled by B. thuringiensis, to find bacterial isolates that were capable of controlling A. aegypti. The 16S ribosomal subunit genes of the selected isolates were sequenced, and the isolates were molecularly characterized based on their Dipteran-specific cry gene contents. Eight of the 76 isolates (10.52%) contained the cry4Aa, cry4Ba or cry10Aa genes, these isolates were carried out against A. aegypti larvae on bioassay. The presence or absence of specific cry genes was associated with the observed average larval mortalities. From the 76 isolates, seven (9.2%) were potentially able to control A. aegypti larvae. Therefore these are promising isolates for the biological control of A. aegypti larvae.


2011 ◽  
Vol 21 (9) ◽  
pp. 1027-1047 ◽  
Author(s):  
Jonathan M. Darbro ◽  
Robert I. Graham ◽  
Brian H. Kay ◽  
Peter A. Ryan ◽  
Matthew B. Thomas

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