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. 2021 Nov 20;46(4):366–372. doi: 10.1584/jpestics.D21-034

Table 1. Properties of the 15 insecticides studied, including mode of action (MoA), registration criteria, SSD parameters (ln Mean, ln SD, and data number n), HC5 (with 90% confidence intervals), and HC50 (with 90% confidence intervals).

Insecticides MoAa) Registration criteria (µg/L) Arthropods HC5 (µg/L) HC50 (µg/L)
ln Mean ln SD n
Methomyl 1A 1.5 4.47 2.08 18 2.7 (0.61–7.7) 88 (39–200)
Acephate 1B 5500 11.10 1.52 11 5000 (920–14000) 66000 (29000–150000)
Trichlorfon 1B 0.11 3.96 1.96 17 2.0 (0.35–6) 53 (22–130)
Malathion 1B 0.3 2.92 2.65 31 0.23 (0.052–0.68) 19 (8.2–42)
Methidathion 1B 0.11 4.03 1.96 9 2.0 (0.15–8.1) 56 (17–190)
Flupyradifurone 4D 6.1 6.88 3.39 5 2.3 (0.00062–61) 970 (38–25000)
Fenbutathin-oxide 12B 0.2 10.53 3.13 6 160 (0.35–2400) 37000 (2800–490000)
BPPS 12C 1.3 8.50 2.95 8 31 (0.4–290) 4900 (680–35000)
Chlorfenapyr 13 0.7 1.96 1.15 8 0.99 (0.18–2.4) 7.1 (3.3–15)
Bensultap 14 20 6.05 2.81 7 3.2 (0.03–32) 420 (53–3300)
Amitraz 19 26 7.90 1.83 8 120 (8–470) 2700 (800–9200)
Tolfenpyrad 21 0.099 1.47 1.85 5 0.16 (0.0019–0.96) 4.3 (0.75–25)
Indoxacarb 22 60 4.94 1.56 6 9.1 (0.43–36) 140 (39–500)
Spiromesifen 23 9.2 5.22 0.71 5 52 (9.4–100) 180 (94–360)
Cyenopyrafen 25 0.29 3.93 1.77 5 2.2 (0.03–12) 51 (9.4–270)

a) IRAC20); 1A, 1B: acetylcholinesterase inhibitors; 4D: nicotinic acetylcholine receptor competitive modulators; 12B, 12C: inhibitors of mitochondrial ATP synthase; 13: uncouplers of oxidative phosphorylation via disruption of the proton gradient; 14: nicotinic acetylcholine receptor channel blockers; 19: octopamine receptor agonists; 21: mitochondrial complex I electron transport inhibitors; 22: voltage-dependent sodium channel blockers; 23: inhibitors of acetyl CoA carboxylase; 25: mitochondrial complex II electron transport inhibitors.