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Additional AB at 1430, 1562, and 1660 cm−1 (Fig. 9) can be explained by overlapping of –OH, CO3 2−, and –COOH groups.
Therefore, presence of two Puf genes in the Plasmodium genome might be explained by overlapping or distinct roles.
On the one hand this may be explained by overlapping functions of PpAOS1 and PpAOS2.
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This have been explained by overlapping phenomena such as competition for nutrients and resources, predation by natural microorganisms and the lack of ability to sustain activity and viability for longer periods (Steenson et al. 1987; Acea et al. 1988; Compeau et al. 1988; Knaebel et al. 1997; Gentry et al. 2004; Owsianiak et al. 2010).
We examined whether the associations among traits were explained by overlapping genetic influences.
Absence of this phenomenon on the experimental spectrum for sol 1 and on the Lorenz fit (Fig. 1a) can be explained by overlap of scattering maxima with the peak 1 at the similar wavelength (384 and 386 nm, respectively).
Alternatively, the missing effects of target eccentricity might be explained by overlaps of the saccade amplitude because of the small visual angles.
Our identification of another region (chr11 3,180,001-3,200,000) can be explained by overlap with a locus previously recognized to be present at higher copy than indicated by the mouse reference genome [ 28].
The presence of a number of carbon atoms (even in the spectrum 3 5 of the inclusions) can be explained by the overlapping of their high content in macromolecular chains of polymer matrix that may partially cover the inclusions.
Co-eluting structures 50, 52, 59, and 60 could be quantified individually by MS. The differences between MS and FLD detection for peaks 62 and 63 can be explained by the overlapping of the two peaks.
We verified that these correlations could not be explained by an overlap in the genes, as the modules exhibited minimal overlap.
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