As shown in Figs 8 and 9, the percentage fluctuation of tracheal NO concentration (the difference between the inspired and expired NO concentrations divided by the inspired concentration) is inversely proportional to the alveolar dead space and directly proportional to the volume of normally aerated pulmonary parenchyma in ARDS [ 13].
For example, some of the peaks in percentage biodiversity fluctuations from 519 150 Ma correspond very closely to the periodicities in extinction identified by [2], [3], [15], and notably we used a different metric than these authors.
There were several instances where our results suggest periodicity in percentage biodiversity fluctuations on the order of roughly 26 30 Myr and thus provide additional confirmation for the arguments of [7], [8], the results of [2], [3], [15], and thus aspects of the more recent analyses by [17], [18].
Moreover, an individual seems to organise the mobility using the TTB as a mobility energy (with the constraint of performing the compulsory daily activities), but keeping the percentage of TTE fluctuations constant.
We detected no effects on the percentage of cells showing fluctuations or the frequency, duration, and amplitude of these fluctuations during exposure to 2 μM 6′-OH-BDE-49 or 3-OH-BDE-47.
During exposure to 0.2 μM 6-OH-BDE-47, we observed an increase in the percentage of cells showing fluctuations.
Exposure to the solvent control [dimethyl sulfoxide (DMSO)] or to 20 μM of BDE-47, BDE-49, BDE-99, BDE-100, or BDE-153 did not decrease cell viability (data not shown) or increase the average or amplitude of [Ca2+] i or the percentage of cells showing fluctuations in [Ca2+] i [see Supplemental Material, Figure 2 (doi:10.1289/ehp.0901339)].
Where, ε is maximum fluctuation limit percentage of SM voltage and it is usually set as 10%%.
In contrast, WSA HSAo show a great fluctuation in percentage of admitted nl-res with a minimum nl% of almost 22% in November and a maximum of 58% in February.
However, the fluctuations in the percentage of appearance of ovigerous females may be attributed to the prevailing environmental fluctuations as recorded in the Red Sea Edwardss, 1987; Morcos, 1990; Hamed & Said, 2000) or to the availability of food (Fusaro, 1978; Fouda, 2000).
