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Finally it is shown that the accuracy obtained by the parabolic case at one hour of sampling rate is similar to the linear case with a sampling rate of five minutes.
Sample pH was measured at room temperature with a combination electrode, which is reliable in solutions with an ionic strength less than 0.1 molal.[11] The sample cooled to room temperature and pH was measured within a half hour of sampling.
Blood was processed within 1 hour of sampling.
The statistical model included the effects of treatment, gender and hour of sampling and their interactions.
In conclusion, hour of sampling was associated with the urinary concentrations of select phthalate metabolites and phenols.
Sample collection occurred every 30 min. The first hour of sampling was discarded to avoid erroneous data due to probe insertion.
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Urine LAM testing was easily performed by trained nurses in an outpatient clinic, returned results within an hour of sample collection, and did not require electricity, reagents, specimen transport, or a highly-trained laboratory microscopist.
Therefore, the ability to extract nucleic acids on-site and within hours of sampling could bypass these two caveats and hasten microbial biofouling assessment and treatment.
Water samples for sulfide isotope composition analyses were filtered through a 0.4 μm Nuclepore Track-Etched Membrane filter within 6 hours of sampling with 20% zinc acetate preservation and frozen on dry ice.
T lymphocyte estimations were performed within eight hours of sampling.
This helped explain why the flies with the most extreme DI values over our 24 hours of sampling were in the CT 13 samples.
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