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All tests were monitored by measuring cell and ferrous iron concentrations, pH and redox potential.
Finally, mutants and R-control strain growth rate were monitored by measuring dry cell weight (DCW) and OD595 values.
Changes in the TAA+ concentration at the interface were monitored by measuring the open circuit potential (OCP).
They were monitored by measuring the spectral changes occurring, respectively, in the visible and UV regions of the dye spectrum.
The penetrant's transport across PVA films were monitored by measuring the time evolutions of through thickness fluorescence intensity profiles.
The temporal changes in the MO concentration were monitored by measuring the UV vis absorption of the MO solution over the photocatalyst at 464 nm (Fig. 6a).
Similar(19)
Growth was monitored by measuring turbidity (OD660).
Growth was monitored by measuring OD at 620 nm.
Growth was monitored by measuring the absorbance at 600 nm.
Pyrite dissolution was monitored by measuring total dissolved iron.
Differentiated osteoblastic function was monitored by measuring alkaline phosphatase activity.
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