Sentence examples for fluctuation derived from from inspiring English sources

Spatial variations of N2O and CH4 fluxes were primarily affected by soil moisture fluctuation derived from astronomic tide, sediment substrate and vegetation composition.

The equation for polymer concentration fluctuation derived from Onuki's equations of motion is coupled with Onuki's postulate for the partial stresses generated by concentration fluctuation to formulate the dynamic structure factor S q,t) [t is time and q the magnitude of the scattering vector].

Location of TEC fluctuations derived from GPS measurements in geomagnetic local time for July and November 2004 storms.

Analysis of the altitude profile of the electron density fluctuations derived from EISCAT data during the global Pc5 wave event has shown that main contribution into the periodic TEC variations is provided by lower ionosphere, up to ~150 km, that is the E-layer and lower F-layer.

As an example, Figs. 10 and 11 show the location of TEC fluctuations derived from GPS measurements in GLT and CGL over different conjugate stations during quiet (July 21 and November 6, 2004) and disturbed (July 27 and November 8, 2004) days for the events under consideration.

Further, Shirts and Pande [81] also showed that using a large number of smaller MD runs could approximate long time-scale fluctuations derived from a single long MD run.

In the present study, we performed a comprehensive modularity analysis of human brain functional networks by examining both temporal and spatial correlation patterns of spontaneous BOLD fluctuations derived from resting-state fMRI.

There are also a few recent studies reporting functional modular organization of spontaneous neuronal activity in the brain networks using spontaneous BOLD fluctuations derived from resting-state fMRI data in the rats [41] and healthy human subjects [42], [43] (we will discuss the similarities and differences among these studies in the Discussion section).

The present work describes a comparison of protein fluctuations obtained from CABS-flex and MD simulations with fluctuations derived from NMR ensembles.

A bin time of 1 ms was chosen throughout to exclude the time-dependent τD1 fluctuation components assigned to fluorescent protein photophysics, whilst retaining slower fluctuations derived from particle diffusion (τD2).

Empirical benchmarking shows relatively high correlations between the native and the predicted with L-pfSeqGNM B-factors and between the cross-correlations of residue fluctuations derived from the structure- and the sequence-based GNM models.