scholarly journals Insect growth regulatory and larvicidal activity of chalcones against Aedes albopictus

2018 ◽  
Vol 48 (1) ◽  
pp. 55-59 ◽  
Author(s):  
Seok-Hee Lee ◽  
Jae Young Choi ◽  
Bo Ram Lee ◽  
Ying Fang ◽  
Jong Hoon Kim ◽  
...  
2016 ◽  
Vol 17 (12) ◽  
pp. 1036-1042
Author(s):  
Prosper C.B. Nya ◽  
Riccardo Moretti ◽  
Marcello Nicoletti ◽  
Maurizio Calvitti ◽  
Lamberto Tomassini

2017 ◽  
Vol 54 (3) ◽  
pp. 670-676 ◽  
Author(s):  
Agustín Alvarez Costa ◽  
Cecilia V. Naspi ◽  
Alejandro Lucia ◽  
Héctor M. Masuh

PLoS ONE ◽  
2018 ◽  
Vol 13 (4) ◽  
pp. e0195681 ◽  
Author(s):  
Temsiri Yooyangket ◽  
Paramaporn Muangpat ◽  
Raxsina Polseela ◽  
Sarunporn Tandhavanant ◽  
Aunchalee Thanwisai ◽  
...  

2020 ◽  
Vol 69 (2) ◽  
pp. 153-160 ◽  
Author(s):  
Le T. Huong ◽  
Trinh T. Huong ◽  
Nguyen T.T. Huong ◽  
Nguyen H. Hung ◽  
Pham T.T. Dat ◽  
...  

2011 ◽  
Vol 109 (1) ◽  
pp. 221-229 ◽  
Author(s):  
Faisal Hafeez ◽  
Waseem Akram ◽  
Essam Abdel-Salam Shaalan

2010 ◽  
Vol 107 (6) ◽  
pp. 1455-1461 ◽  
Author(s):  
Barbara Conti ◽  
Angelo Canale ◽  
Alessandra Bertoli ◽  
Francesca Gozzini ◽  
Luisa Pistelli

2015 ◽  
Vol 52 (2) ◽  
pp. 199-206 ◽  
Author(s):  
K. W. Lau ◽  
C. D. Chen ◽  
H. L. Lee ◽  
Y. Norma-Rashid ◽  
M. Sofian-Azirun

2020 ◽  
Vol 36 (1) ◽  
pp. 11-15
Author(s):  
Megan N. Rhyne ◽  
Stephanie L. Richards

ABSTRACT Aedes albopictus is a vector of several arboviruses; however, control of this day-active species is difficult with ultra-low-volume insecticide treatments applied at dusk/dawn periods. In the current laboratory study, blood-fed Ae. albopictus were exposed to Archer® (insect growth regulator AI: pyriproxyfen) residue in glass bottles (to approximate barrier treatment) and allowed to oviposit. Control mosquitoes were exposed to clean bottles. To evaluate potential dilution effects of water volume, mosquitoes were allowed to oviposit in (relatively) small (59 ml water) or large (177 ml water) containers. The extent to which fecundity (number of eggs laid), fertility rate (number of larvae hatched/number of eggs laid × 100), and emergence rate (number of adults emerged/number of larvae hatched × 100) differed between groups was characterized. In the control group, 18–21 (82–95%) mosquitoes laid eggs, while only 10–11 (45–50%) of mosquitoes in the pyriproxyfen group laid eggs. These sample sizes should be considered when comparing results to other studies. Significantly lower (P = 0.0008) fecundity was observed in mosquitoes exposed to pyriproxyfen (mean ± SE) (small container: 25.2 ± 7.1, large container: 24.3 ± 7.1) compared to control mosquitoes (small container: 49.2 ± 7.8, large container: 52.7 ± 5.2). Regardless of treatment, no significant differences in fecundity were observed between mosquitoes allowed to oviposit in different-sized containers. Hatch rate was significantly lower in the pyriproxyfen group and was impacted by container size (P = 0.032) and treatment (P < 0.0001) (large, control: 61.9% ± 7.8; small, control: 38.0% ± 7.1; large, treated: 10.3% ± 2.4; small, treated: 2.9% ± 1.9). Adult emergence rates were not significantly impacted by treatment or container size. Pyriproxyfen applied as a barrier treatment may be an effective tool for controlling Ae. albopictus.


Author(s):  
T.D.H. Dinh ◽  
Q.T. Le ◽  
T.D. Nguyen ◽  
T.Q.T. Nguyen ◽  
A.S. Ho ◽  
...  

A Vietnamese domestic plant namely Solanum nigrum (S. nigrum) was subjected to test for larvicidal activity on two majors Dengue hemorrhagic fever (DHF) vectors Aedes aegypti (Ae. aegypti) and Aedes albopictus (Ae. albopictus). The plant was processed to get infusions in hot water or extracted in ethanol. Laboratory and field larval strains of two Aedes species were exposed to the infusions and extract at increasing concentrations for one hour and followed-up intensively for up to 72 hours. The obtained results of bioassay showed larvicidal effects of extract on all mosquito strains. The effects on laboratory strain of Ae. aegypti larvae were correlated with infusions and extract concentrations. Chopped plant infusions in hot water indicated mortality up to 77.3% of larvae. Ground plant infusions killed all of exposed larvae at day 3 postexposure. Median lethal concentrations (LC50,s) of chopped and ground plant infusions were 10.25 and 7.54%, respectively. Ethanolic extract had very strong effect on experimental subjects. Within 72 hours, 100% of laboratory strain of Ae. aegypti larvae died after exposure to extract at 100 parts per million (ppm) or higher concentrations. Ethanolic plant extract showed similar larvicidal effect on field strains of Ae. aegypti and Ae. albopictus. The percentage mortality of field strains larvae reached 100% after exposure to 100 ppm of plant extract. At concentrations of 1000 ppm, 100% of exposed larvae died with 8 hours. LC50 on tested larvae was 25.07-33.60 ppm. Strong larvicidal activity of S. nigrum suggests the possible application in DHF vector control effort.


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