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FISH experiments were performed using 8-chambered slides, with 2 replicates of 100 cells each inspected per chamber.
In the first experiment, two treatments were compared using three replicates of two birds per chamber.
Branson et al. [9] quantifies behaviour of multiple flies, while our system is specifically optimized for two flies per chamber.
Mass and nicotine values are the mean of three QCMs per chamber and three replicate experiments per product and dilution.
We tested between four to 32 seeds per chamber (air volume = 14 mL) and after 36 h measured the root length.
The MWPC parameters: efficiency – 30%, width of channel – 0.6 mm, total number of channels – 640, maximum counting rate per chamber – 3×108 counts/s.
The study was initiated with < 24-h-old Daphnia (1 daphnid per chamber) that were exposed to hydrogen peroxide for 21 days.
The spark rate of the detectors was very low and decreased with time to an average of one spark per chamber per day.
The lower surfaces (with migrant cells) were captured by photomicroscopy (BX51 Olympus, Japan), and the cells were blindly counted (five fields per chamber).
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However, we found no evidence for increased antheridium-per-chamber numbers in dioicous species.
However, we found no evidence of increased antheridium-per-chamber numbers in dioicous species.
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