Induction of chymoelastase (Pr1) of <Emphasis Type="Italic">Metarhizium anisopliae</Emphasis> and its role in causing mortality to mosquito larvae

The efficacy of virulent strain Metarhizium anisopliae 892 obtained from Pyrausta nubilalis was evaluated against mosquito larvae. LC₅₀ values of M. anisopliae 892 for Culex quinquefasciatus, Anopheles stephensi and Aedes aegypti were compared. Metarhizium anisopliae 892 could cause approximately 50% mortality of C. quinquefasciatus 4 days post inoculation in the concentration of 3.48 × 10³ conidia/ml. The production of cuticle degrading enzyme chymoelastase (Pr1) and trypsin like protease (Pr2) was compared in the presence of inducers. There were significant differences in the production of Pr1 and Pr2 after addition of inducers i.e. cuticles of the three mosquito. The cuticles of C. quinquefasciatus induced maximum Pr1 in the mycelia of M. anisopliae 892 than the rest of two mosquito cuticles during de-repression condition. The larvae of C. quinquefasciatus were more susceptible than the larvae of A. stephensi and A. aegypti against spores of M. anisopliae 892. The quantity of induction of Pr1 in the mycelia of M. anisopliae 892 was positively correlated with the mortality of mosquito larvae. Production of Pr1 and Pr2 was decreased when the inducers were de-proteinated cuticles. The Pr2 induction of M. anisopliae 892 did not correlate with the mortality of mosquito larvae. From the observations of the present study it can concluded that Pr1 is a responsible factor for the mortality of the mosquito larvae. This is the first report of Pr1 induction by mosquito cuticle and its role in mosquito mortality.     

Drinking rate regulation in some fresh-water mosquito larvae

ABSTRACT. Drinking rates were determined with four species of freshwater mosquito larvae by colorimetric measurement of the dye ingested after groups of fourth instars were allowed access for set periods to 2% amaranth solutions. The rate of drinking for the saline-tolerant Aedes aegypti, 309±113 nl per h per individual, was comparable with rates given in the literature for several saline-water species, but rates for Culex quinquefasciatus, Culex molestus and Anopheles albimanus were markedly lower (167±30, 48±17 and 108±28m per h, respectively). When larvae of A.aegypti and C. quinquefasciatus were glutted with kaolin (allowed to replace all food in the gut by filter-feeding in kaolin suspension), drinking rates were little affected at first, but after 1 day of fasting (holding in water after glutting), drinking rates were 50% lower and were reduced by a further 20% with fasting for up to 3 days. For A.aegypti, C.quinquefasciatus and C. molestus, drinking rates were approximately doubled with kaolin dispersed in the dye solution, and after fasting, were increased by up to 100% in solutions containing 0.05% of water-soluble yeast extract. A similar phagostimulant effect of 10^-3M adenylic acid was demonstrated for A. aegypti and C. quinquefasciatus. A single experiment indicated similar stimulatory effects of kaolin and adenylic acid for, A. albimanus. With 0.01-0.05% agarose in the dye solutions, drinking rates for A. aegypti and C. quinquefasciatus were more than doubled, and a similar though weaker effect was demonstrated for another colloid, methylcellulose. In constrast, both colloids markedly reduced the rate of drinking with A.albimanus. These findings are discussed in relation to whether drinking and filter-feeding are necessarily coupled. The possible significance of this with respect to larvae that feed in different microhabitats, providing different levels of dissolved and colloidal nutrient organic matter, is considered. The implications of drinking rates for biotests of solubilized bacterial toxins as mosquito larvicides are noted.     

Biochemical and cytoimmunological evidence for the control of Aedes aegypti larval trypsin with Aea-TMOF

Trypsin and chymotrypsin-like enzymes were detected in the gut of Aedes aegypti in the four larval instar and pupal developmental stages. Although overall the amount of trypsin synthesized in the larval gut was 2-fold higher than chymotrypsin, both enzymes are important in food digestion. Feeding Aea-Trypsin Modulating Oostatic Factor (TMOF) to Ae. aegypti and Culex quinquefasciatus larvae inhibited trypsin biosynthesis in the larval gut, stunted larval growth and development, and caused mortality. Aea-TMOF induced mortality in Ae. aegypti, Cx. quinquefasciatus, Culex nigripalpus, Anopheles quadrimaculatus, and Aedes taeniorhynchus larvae, indicating that many mosquito species have a TMOF-like hormone. The differences in potency of TMOF on different mosquito species suggest that analogues in other species are similar but may differ in amino acid sequence or are transported differently through the gut. Feeding of 29 different Aea-TMOF analogues to mosquito larvae indicated that full biological activity of the hormone is achieved with the tetrapeptide YDPA. Using cytoimmunochemical analysis, intrinsic TMOF was localized to ganglia of the central nervous system in larvae and male and female Ae. aegypti adults. The subesophageal, thoracic, and abdominal ganglia of both larval and adult mosquitoes contained immunoreactive cells. Immunoreactive cells were absent in the corpus cardiacum of newly molted 4th instar larvae but were found in late 4th instar larvae. In both males and females, the intrinsic neurosecretory cells of the corpus cardiacum were filled with densely stained immunoreactive material. These results indicate that TMOF-immunoreactive material is synthesized in sugar-fed male and female adults and larvae by the central nervous system cells.     

Expression of the Bacillus thuringiensis Mosquitocidal Toxin Cry11Aa in the Aquatic Bacterium Asticcacaulis excentricus

A mosquitocidal aquatic bacterium has been developed by introducing an operon containing the cry11Aa, and p20 genes from Bacillus thuringiensis subsp. israelensis (Bti) into the gram-negative aquatic bacterium Asticcacaulis excentricus. After transformation, the cry11Aa gene was successfully expressed in recombinant A. excentricus under the tac promoter, at the level of 0.04 pg/cell. The recombinant bacteria were toxic to Aedes aegypti larvae with an LC₅₀ of 6.83 × 10⁵ cells/mL. We believe that these bacteria may have potential as genetically engineered microorganisms for the control of mosquito larvae.     

Synergistic activity of Bacillus thuringiensis δ‐endotoxin and TMOF against Culex pipiens and Spodoptera littoralis larvae

Trypsin Modulating Oostatic Factor (TMOF) is a decapeptide hormone that inhibits the biosynthesis of digestive enzymes in the mosquito midgut. The hormone inhibits food digestion and ultimately leads to starvation and death. It has been used as a biological insecticide to control mosquitoes. In an attempt to increase the insecticidal activity of TMOF, a combination of CryIC (δ‐endotoxin from Bacillus thuringiensis) and TMOF was determined. Eight recombinant proteins fused with GST (glutathione‐S‐transferase) were expressed in Escherichia coli cells. Their insecticidal activities were determined against Culex pipiens and Spodoptera littoralis larvae. Purified GST‐TMOF and its analogue GST‐YDPAS exhibited a moderate toxicity on C. pipiens larvae with LC₅₀ of 145.9 and 339.9 μg/mL, respectively. Unexpectedly, no mortality was observed in first instar larvae of S. littoralis. Puirified GST‐TMOF and GST‐YDPAS together with Bt toxin showed a synergistic toxic effect on both Culex and Spodoptera larvae. In the presence of 100 μg/mL GST‐TMOF and GST‐YDPAS, the median lethal concentration of entomocidus on culex larvae decreased from 52.1 to 16.7 and 31.9 μg/mL, respectively. Likewise, GST‐TMOF and GST‐YDPAS incorporated with 0.07 μg/cm² of enotmocidus showed insecticidal activity against S. littoralis with LC₅₀ of 16.4 and 21.9 μg/cm². The E. coli lysates containing GST‐CryIC and its 3′‐truncated version showed low toxicity against the lepidopteran insect (10.8 and 16.6 μg/cm²) compared to 0.15 μg/cm² of the native crystalline form of CryIC. Similarly, the mosquitocidal activity of the recombinant Bt toxins was low.     

Oostatic peptides

Oostatic peptides are organic molecules, which influence an insect reproduction due to a regulation of the eggs development. It was proved that decapeptide—H-Tyr-Asp-Pro-Ala-Pro-Pro-Pro-Pro-Pro-Pro-OH (YDPAPPPPPP)—isolated from mosquito Aedes aegypti, inhibits trypsin activity in the midgut of the mosquito. Therefore, it was named trypsin-modulating oostatic factor (Aea-TMOF). Feeding the recombinant cells with cloned and expressed TMOF on the coat protein of tobacco mosaic virus (TMV) to mosquito larvae, caused larval mortality. The TMOF was therefore designed for usage as a new biorational insecticide against mosquito. Similarly, a hexapeptide—H-Asn-Pro-Thr-Asn-Leu-His-OH (NPTNLH)—was isolated from the grey flesh fly Neobellieria bullata. This peptide and some of its analogs inhibited trypsin-like synthesis by the midgut in female flies and was therefore entitled Neb-TMOF. Interestingly, the synthetic Aea-TMOF and mainly its C-terminus shorten analogs, including those containing D-amino acids or methylene-oxy isosteric bond, quickly and strongly inhibited the hatchability and egg development in the flesh fly N. bullata.     

Biolarvicidal activity of extracellular metabolites of the keratinophilic fungus <Emphasis Type="Italic">Trichophyton mentagrophytes</Emphasis> against arvae of <Emphasis Type="Italic">Aedes aegypti</Emphasis> — a major vector for Chikungunya and dengue

The larvicidal activity of extracellular metabolites of keratinophilic fungus Trichophyton mentagrophytes against Aedes aegypti larvae was determined. T. mentagrophytes was isolated from soil by the feather baiting technique. Culture filtrates (10–100 μL/mL) were found to be entomotoxic to 3rd instars larvae of A. aegypti (L3), LC₅₀ and LC₉₀ being 110 ± 11.5 and 200 ± 20.7 μL/mL, respectively, after 2 d. Extracellular metabolites are proteinaceous in nature and more specific to chitin of mosquito larvae. They degraded cock feather causing an average of 20.0 ± 2.6 % loss in feather mass. Culture filtrate at 100 μL/mL produced 90 % mortality against L3 after 3 d; mortality was increased in dose- and time-dependent manner. These extracellular metabolites of T. mentagrophytes could be regarded as alternatives to synthetic insecticides.     

Evaluation of a granular formulation containing Metarhizium brunneum F52 (Hypocreales: Clavicipitaceae) microsclerotia in controlling eggs of Aedes aegypti (Diptera: Culicidae)

We evaluated the potential of a granular formulation of Metarhizium brunneum F52 containing microsclerotia (MbMSc granules) for control of Aedes aegypti by targeting eggs. MbMSc granules produced infective conidia within 14 days after application to 2.5?g moist potting soil, producing 5.9?×?10⁵, 2.08?×?10⁶ and 6.85?×?10⁶ conidia from 1, 5 and 25?mg MbMSc granules, respectively. Application of MbMSc triggered premature eclosion of eggs (EC_50?=?12?mg) with percentages as high as 31?±?2.9% and 67?±?4.3% of the eggs treated with 5 and 25?mg MbMSc granules, respectively, after 14 days on moist filter paper. Premature eclosion of eggs started at 3 days subsequent to MbMSc granule application and survival of larvae was significantly reduced for granule treated eggs (74?±?2.2%, 39?±?2.0% and 23?±?4.9% larvae survived for 1, 5 and 25?mg granule treatments, respectively, EC₅₀?=?4.9?mg). When MbMSc granules were applied in moist potting soil with mosquito eggs, rates of 1, 5 and 25?mg of MbMSc granules significantly reduced adult emergence with only 81?±?2.1%, 47?±?1.9%, and 34?±?2.1% emergence, respectively (EC₅₀?=?7?mg). Eggs treated with increasing concentrations of fungal conidia enhanced premature eclosion of eggs with an EC₅₀?=?1.6?×?10⁶ conidia/mL. Our results demonstrate that MbMSc granules are a promising candidate for control of A. aegypti and that fermentative production of Mb F52 microsclerotia as the active propagule has the potential for use for mosquito control.     

Lifetable demography and population growth of the rotifer Brachionus angularis in Kenya: influence of temperature and food density

Lifetable demography and reproductive traits of a Kenyan strain of the rotifer Brachionus angularis were investigated using individual and small batch culture approaches. The rotifer was identified morphologically before conducting studies at 20, 25 and 30 °C, using Chlorella vulgaris at 2.5 × 10⁵ to 2.5 × 10⁷ cells ml^–1. The rotifers were highly fecund, producing 2.11 ± 0.07 offspring female^–1 day^–1 and reproductive, producing 8.43 ± 0.24 offspring female^–1 at 25 °C with 2.5 × 10⁶ algal cells ml^–1. The highest intrinsic rate of natural increase (0.74 ± 0.02 d^–1), specific population growth rate (0.49 ± 0.01), longest life expectancy at hatching (12.41 ± 0.28 d) and shortest generation time (2.87 ± 0.03 d) also occurred at 25 °C with 2.5 × 10⁶ algal cells ml^–1. The duration of hatching to first spawning was shortest (2.86 ± 0.21 h) at 30 °C with 2.5 × 10⁷ algal cells ml^–1 and longest (8.83 ± 0.39 h) at 20 °C with 2.5 × 10⁵ algal cells ml^–1. The highest population density (255.7 ± 12.6 ind. ml^–1) was realised at 25 °C with 2.5 × 10⁶ cells ml^–1 on Day 8, whereas the lowest population density (122.0 ± 3.6 ind. ml^–1) was realised at 20 °C with 2.5 × 10⁵ cells ml^–1 on Day 8. The lorica length and width of the Kenyan strain of B. angularis are 85.6 ± 3.1 µm and 75.4 ± 3.6 µm, respectively. The rotifer optimally reproduces at 25 °C when fed with 2.5 × 10⁶ algal cells ml^–1.     

Synthesis and larvicidal activity of indole derivatives against Aedes aegypti (Diptera: Culicidae)

In light of the challenges to control Aedes aegypti and the critical role that it plays as arbovirus vector, it is imperative to adopt strategies that provide fast, efficient and environmentally safe control of the insect population. In the present study, we synthesized six indole derivatives (C1‐C6) and examined their larvicidal activity and persistence against Ae. aegypti larvae, as well as their toxicity towards Raw 264.7 macrophages, Vero cells, Chlorella vulgaris BR017, Scenedesmus obliquus BR003, Caenorhabditis elegans N2 and Galleria mellonella. Among the bioactive compounds (C1, C2, C4 and C5), C2 exerted the strongest larvicidal activity against Ae. aegypti, with LC50 = 1.5 μg/ml (5.88 µM) and LC90 = 2.4 μg/ml (9.50 µM), indicating that the presence of chlorine or bromine groups in the aromatic ring improved the larvicidal activity of the indole derivatives. C1, C2, C4 and C5 did not reduce viability of RAW 264.7 macrophages, Vero cells, C. elegans N2 and G. mellonella. Compounds C1, C2 and C5 did not affect the growth of C. vulgaris BR017 and S. obliquus BR003. Analysis of larvicidal persistence under laboratory conditions revealed that the effect of compounds C1, C2, C4 and C5 lasted for 30 days and caused 100% of larvae mortality within few hours. Altogether, our findings demonstrate that the indole derivatives C1, C2, C4 and C5 effectively control Ae. aegypti larvae population, without clear signs of toxicity to mammalian cells, algae, C. elegans and G. mellonella.     

Efficient expression of mosquito-larvicidal proteins in a gram-negative bacterium capable of recolonization in the guts of Anopheles dirus larva

The gram-negative bacterium, An11/2 G1, isolated from the guts of Anopheles dirus mosquito larvae, was identified as Enterobacter amnigenus. The E. amnigenus was able to recolonize in the gut of An. dirus larva but not in those of Aedes aegypti and Culex quinquefasciatus larvae. It was able to float in water for a longer period than Bacillus thuringiensis subsp. israelensis and Bacillus sphaericus. These are desirable characteristics for a delivery vehicle of mosquito-larvicidal toxins for the control of mosquito larvae, and E. amnigenus was therefore used as a host to express the cryIVB gene of B. thuringiensis subsp. israelensis and the binary toxin genes of B. sphaericus. The recombinant E. amnigenus produced a high level of CryIVB protein, which was toxic to larvae of Ae. aegypti and An. dirus. Another E. amnigenus producing the 51-kDa protein of B. sphaericus was toxic to larvae of An. dirus and Cx. quinquefasciatus. The recombinant plasmids were stable in E. amnigenus without the presence of selective pressure for at least 23 generations. The recombinant E. amnigenus should represent a desirable biological agent for controlling mosquito larvae. Received: 20 February 1998 / Received last revision: 5 October 1998 / Accepted: 11 October 1998     

Effect of selected marine and freshwater microalgae on development and survival of the mosquito <Emphasis Type="Italic">Aedes aegypti</Emphasis>

We isolated and identified strains of marine and freshwater planktonic and benthic microalgae from the vicinity of Indian River County, Florida (≈27.5°N, 80.34°W), cultivated them in batch culture, and examined their allelopathic activity against mosquito larvae. Additional algal material was obtained from Syracuse University and the University of Texas—Austin Algal Culture Collection. Mosquito larvae (Aedes aegypti (L.)) from colonies maintained at the Florida Medical Entomology Laboratory were challenged with the microalgae using log-growth phase and senescent-phase cultures. Appropriate controls (no algae) were used for each treatment. There were no significant differences in development time between treatments across all trials and a few significant treatment effects on development times, mortality, or mosquito size in the individual trials; however, there was a tendency for treatments with senescent microalgae to develop faster than controls with no algae. Effects consistent with algal toxicity included the two trials with Microcystis aeruginosa, where the larvae exposed to the strain-producing microcystin had significantly longer development times than the controls or those grown with the non-microcystin-producing strain, and the trial with the dinoflagellate Akashiwo sanguinea, where larvae exposed to this species had significantly higher mortality than the controls. No consistent patterns or differences between experimental and control treatments in the value of λ′, an estimate of the population finite rate of increase, were discernible from the data.     

Mosquitoes of Rarotonga,Cook Islands: A survey of breeding sites

Abstract

Two surveys of Rarotonga, Cook Islands (21°20^'S, 160°16^'W) were made to determine the mosquito fauna of the island, and to identify the habitats required for breeding by searching for larvae. The first survey was made during the “dry season” in May 2001, the second during the “wet season” in February 2002. The mosquito fauna comprised four species Culex (Culex) quinquefasciatus Say, Culex (Culex) annulirostris Skuse, Aedes (Stego‐myia) aegypti (Linnaeus) and Aedes (Stegomyia) polynesiensis Marks. Larvae of the Culex species were most often found in larger natural and artificial water bodies. The Aedes species bred in both natural and artificial containers of all sizes. Ae. polynesiensis was the most widespread species, using natural holes in all regions as well as artificial containers in the urban areas. Most larvae of Ae. aegypti were located in small artificial containers. The two Aedes species are the vectors of dengue fever on the island. Mosquito control during outbreaks should specifically target the artificial containers preferred by Aedes sp. for breeding habitats.     

Determination of mosquito Larvicidal potential of <Emphasis Type="Italic">Bacillus thuringiensis</Emphasis> Cry11Ba fusion protein through molecular docking

Mosquitoes spread deadly infections around the world. Since decades Bacillus thuringiensis (Bt) δ-endotoxins have been used successfully as a biopesticide for controlling mosquito larvae. However, over a few years, mosquito larvae have evolved tolerance against Bt δ-endotoxins, rendering them ineffective for mosquito control. Such a problem entails the development of improved toxins with enhanced toxicity, affinity towards a wide range of mosquito receptors and ability to overcome or delay the resistance buildup. In this study, using in silico tools, we aimed to design a fusion protein by fusing active region of Bt subsp. jegathesan Cry11Ba protein with Aedes aegypti TMOF (trypsin modulating oostatic factor). Using computational study, the fusion protein was validated and its mosquitocidal potential was determined through molecular docking against cadherin and aminopeptidase N midgut receptors of Aedes aegypti, Anopheles gambiae and Culex quinquefasciatus. Molecular docking revealed that from Cry11Ba-TMOF fusion protein, domain II amino acids of Cry11Ba protein showed hydrogen bond interactions with cadherin and aminopeptidase N receptors of the targeted mosquitoes. These results conclude that Cry11Ba-TMOF fusion protein has a strong affinity for the receptors of Ae.aegypti, An.gambiae and Cx.quinquefasciatus. Thus the designed fusion protein can be used as a potent mosquitocidal agent for the control of targeted mosquitoes.     

The relative importance and distribution of Aedes polynesiensis and Ae.aegypti larval habitats in Samoa

Abstract. In preparation for a Filariasis Control programme in Samoa, during 1978 monthly larval surveys of the vector mosquito Aedes polynesiensis were carried out in four study villages in the main island of Upolu. A more extensive survey of larval habitat distribution was then made in twenty-two villages of Upolu and eighteen of Savai'i island, to determine the importance of habitat types according to their abundance, volume of water and whether their productivity was permanent or seasonal. Ae.aegypti larval densities and habitat distribution were also monitored and the occurrence of predatory Toxorhynchites amboinensis larvae in northern Upolu was recorded from forty-one collections. Aedes Breteau and container indices fluctuated with the pattern of rainfall in two coastal villages and an inland bush village, but not in a coconut plantation community. The five main Aedes larval habitat types encountered were: 200 litre water-storage drums, discarded tins and bottles, coconut shells, automobile tyres and treeholes. Aedes immatures occurred perennially in drums and tree holes, but breeding discontinued in tins, bottles and coconut shells during the driest month of July. For Ae.polynesiensis in Upolu the Breteau and container indices of 104.5 ± SD 80.9 and 35.3 ± 12.4 respectively were significantly higher than those in Savai'i: 33.1 ±25.0 and 24.3 ±20.0 respectively. Likewise for Ae.aegypti the Breteau and container indices of 50.8 ± 32.5 and 23.9 ± 15.6, respectively, were also significantly higher than those in Savai'i: 12.7 ± 17.1 and 9.4 ±13.2 respectively. Habitat types greater or lesser importance were determined by plotting the percentage of each type of container utilized for Aedes breeding against the percentage of each type amongst all larva-positive containers. Ae.polynesiensis preferred tree-holes but not water-storage drums. Ae.aegypti preferred drums and tyres; mixed populations of larvae of both species were commonest in these two types of habitat. Ae.polynesiensis occurred in every village. Ae.aegypti was encountered in all twenty-two villages surveyed in Upolu and nine of eighteen villages in Savai'i. Total larval surveys revealed that drums and tree-holes contained the highest numbers of Aedes larvae. The study provided criteria for planning a control programme.     

Comparative study of hemolymph phenoloxidase activity in Aedes aegypti and Anopheles quadrimaculatus and its role in encapsulation of Brugia malayi microfilariae

Hemolymph phenoloxidase activity of sugar-fed and blood-fed females of Anopheles quadrimaculatus and Aedes aegypti showed similar characteristics. Phenoloxidase was present as an inactive proenzyme in both mosquito species and was partially activated during collection of the hemolymph. In both mosquito species, phenoloxidase activity was modulated by different buffers and activated phenoloxidase did not need Ca²⁺. Enzymatic activity was higher in the hemocytes than in the plasma in both mosquito species. Trypsin, laminarin, and blood-feeding on uninfected and Brugia malayi-infected jirds enhanced hemolymph phenoloxidase activity in both mosquito species. The appearance of hemolymph phenoloxidase activity was inhibited by p-nitrophenyl p′-guanidinobenzoate HCl, soybean trypsin inhibitor, ethylenediaminetetraacetic acid, diethyldithiocarbamic acid, saturated 1-phenyl-2-thiourea and reduced glutathione, but not by benzamidine in A. quadrimaculatus. The appearance of hemolymph phenoloxidase activity was inhibited by benzamidine, diethyldithiocarbamic acid, saturated 1-phenyl-2-thiourea, reduced glutathione, β-nitrophenyl p′-guanidinobenzoate and soybean trypsin inhibitor, but not by ethylenediaminetetraacetic acid in A. aegypti. It is suggested that in both mosquito species, blood-feeding and migration of sheathed microfilariae in the homocoel activated the prophenoloxidase in the hemolymph and caused the encapsulation and melanization of microfilarial sheaths and microfilariae of B. malayi.     

The effects of light intensity and algae-induced turbidity on feeding behaviour of larval striped trumpeter

Striped trumpeter larvae reared in algal cell‐induced turbid water (greenwater) fed equally well in clearwater in a light intensity range of 1–10 μmol s^‐1 m^‐2, when evaluated in terms of both the proportion of larvae feeding and larval feeding intensity. An ontogenetic improvement in photopic visual sensitivity of larvae was indicated by improved feeding at 0·1 μmol s^‐1 m^‐2, from 26±5% of larvae feeding and 0·027±0·005 rotifers consumed per feeding larva min^‐1 on day 8, to 96±2% and 0·221±0·007 rotifers consumed larva^‐1 min^‐1 on day 23 post‐hatching. Algal cell‐induced turbidity was shown to reduce incident irradiance with depth, indicated by increasing coefficients of attenuation (1·4–33·1) with increasing cell densities (0–2×10⁶ cells ml^‐1), though light intensities in the feeding experiment test chambers, at the algal cell densities tested, were within the optimal range for feeding (1–10 μmol s^‐1 m^‐2). Algae‐induced turbidity had different effects on larval feeding response dependent upon the previous visual environment of the larvae. Young larvae (day 9 post‐hatching) reared in clearwater showed decreased feeding capabilities with increasing turbidity, from 98±1% feeding and 0·153±0·022 rotifers consumed larva^‐1 min^‐1 in clearwater to 61±10% feeding and 0·042±0·004 rotifers consumed larva^‐1 min^‐1 at 56 NTU, while older clearwater reared larvae fed well at all turbidities tested. Likewise, greenwater reared larvae had increased feeding capabilities in the highest algal cell densities tested (32 and 66 NTU) compared with those in low algal cell density (6 NTU), and clearwater (0·7 NTU) to which they were naïve.     

A field test for competitive effects of<Emphasis Type="Italic"> Aedes albopictus</Emphasis> on<Emphasis Type="Italic"> A. aegypti</Emphasis> in South Florida: differences between sites of coexistence and exclusion?

We tested whether interspecific competition from Aedes albopictus had measurable effects on A. aegypti at the typical numbers of larval mosquitoes found in cemetery vases in south Florida. We also tested whether the effect of interspecific competition from A. albopictus on A. aegypti differed between sites where A. aegypti either persists or went extinct following invasion by A. albopictus. Similar experiments manipulating numbers of A. albopictus in cemetery vases were conducted at three sites of A. aegypti persistence and three sites where A. aegypti was apparently extinct. The experiments were done using numbers of larvae that were determined by observed numbers of larvae for each site, and with resources (leaf detritus) that accumulated in experimental vases placed into each field site. In both the early rainy season (when number of mosquito larvae was low) and the late rainy season (when number of mosquito larvae was high), there was a significant effect of treatment on developmental progress of experimental A. aegypti. In the late rainy season, when numbers of larvae were high, there was also a significant effect of treatment on survivorship of A. aegypti. However, the competition treatment × site type (A. aegypti persists vs extinct) interaction was never significant, indicating that the competitive effect of A. albopictus on A. aegypti did not differ systematically between persistence versus extinction sites. Thus, although competition from A. albopictus is strong under field conditions at all sites, we find no evidence that variation in the impact of interspecific competition is associated with coexistence or exclusion. Interspecific competition among larvae is thus a viable explanation for exclusion or reduction of A. aegypti in south Florida, but variation in the persistence of A. aegypti following invasion does not seem to be primarily a product of variation in the conditions in the aquatic environments of cemetery vases.     

Effects of a larval mosquito biopesticide and Culex larvae on a freshwater nanophytoplankton (Selenastrum capricornatum) under axenic conditions

The effects of microbial biopesticides used for mosquito control on autotrophic microorganisms such as nanophytoplankton are equivocal. We examined impacts of mosquito biopesticides and mosquito larvae on primary producers in two independent experiments. In the first experiment, we examined the effects of a commonly used microbial biopesticide formulation (VectoMax^® CG) on a unicellular microalga, Selenastrum capricornatum Printz, under axenic laboratory conditions. The biopesticide treatments included two concentrations (0.008 and 0.016 g liter^?1) of VectoMax^® CG and two controls (one untreated and another with autoclaved 0.016 g VectoMax^® CG liter^?1) in replicated axenic experimental microcosms. Spectrophotometric analysis of chlorophyll a (proxy for algal biomass) and direct enumeration of algal cells following the treatments revealed no significant effects of the microbial biopesticide on algal population growth during the four‐week study. In the second experiment, we tested the effects of different densities of Culex larvae on the population of S. capricornatum. Effects of mosquito larvae feeding on S. capricornatum were significant with a curvilinear relationship between larval density and algal abundance in the water column. Together, these studies demonstrated a lack of direct cytological/toxicological effects of Bacillus‐based microbial pesticides on freshwater primary production and support the hypothesis that the reduction in algal primary production previously reported when Bti products were applied to aquatic environments was likely independent of the Bacillus‐based larvicidal toxins. Instead, it was likely mediated by microbial interactions in the water column and the trophic cascade effects that resulted from the removal of larval mosquitoes. These studies suggest that mosquito larvae independent of pesticide application can influence primary production. Our method of evaluating biopesticides against small photoautotrophs can be very useful for studying the unintended effects on autotrophic microorganisms of other pesticides, including herbicides and pesticides applied to aquatic environments.     

Selective and frequency dependent predation of aquatic mosquito predator Diplonychus indicus Venkatesan & Rao (Hemiptera: Belostomatidae) on immature stages of three mosquito species

Frequency dependent mosquito larval size (II and IV instars) and species selection by the water bug Diplonychus indicus against three mosquito species Culex quinquefasciatus, Aedes aegypti and Anopheles stephensi was studied in the laboratory. The different frequencies used for each species selection were 20:30:50, 30:50:20, 50:20:30, 25:35:40, 35:40:25 and 40:25:35 of fourth instars of the respective three prey species. All nymphal water bugs (I–V instars) selected IV instar mosquito larvae and the mean proportion of late (larger) larvae eaten by the predator instars was significantly higher than the mean proportion of early (smaller) larvae eaten (F= 2.28; P < 0.001). In all six ratios used to determine the frequency dependent mosquito species selection, all the stages of the water bug selected Ae. aegypti over the other two species (F= 452.43; P < 0.001). The mean number of mosquito larvae eaten increased as its density increased based on various ratios of larvae offered. The study indicated that the predatory efficiency of D. indicus was high when Ae. aegypti was offered as prey, suggesting the utility of this mosquito predator in the control of dengue vectors.