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Two‐part experimental design. Part 1 consisted of four treatment solutions containing 0 µg/L carbaryl + low resources, 0.05 µg/L carbaryl + low resources, 0 µg/L carbaryl + high resources, and 0.05 µg/L carbaryl + high resources. During part 2, we initiated the TTD assay by exposing D. pulex from each of the four Part 1 treatments to either a control or lethal concentration of carbaryl (15 µg/L)
