Contact toxicity/aphid dip bioassay

MA Maqsood Ahmed
QP Qin Peiwen
ZG Zumin Gu
YL Yuyang Liu
AS Aatika Sikandar
DH Dilbar Hussain
AJ Ansar Javeed
JS Jamil Shafi
MI Mazher Farid Iqbal
RA Ran An
HG Hongxia Guo
YD Ying Du
WW Weijing Wang
YZ Yumeng Zhang
MJ Mingshan Ji
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A 30 mm diameter plastic Petri dish was cut from the basal portion, and the remaining ring was used as the container. A nematode strainer (mesh size 300 µm) was used as a holding cell for aphids during dipping into the plant extracts of varying concentration (Fig. 2). Then, twenty aphids at second instar were isolated from the cabbage plants and dipped in the extracts for 10 s. Each group of dipped aphids was then placed on fresh 5 cm diameter cut leaf discs on agar-containing Petri dishes. The negative control treatment was prepared using the Tween-20 (5%) solution as described above but without adding plant extract. An imidacloprid solution of 20% SL (2.5 mL L−1) was used as a positive control. All Petri dishes were incubated for 72 h at 65% R.H., 25 °C and with a 16:8 (light: dark) photoperiod.

Containers utilized for contact bioassay.

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