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These complex patterns of asymmetry reflect different combinations of controls including discharge partitioning, lobe abandonment and localized transgression, plume deflection by coastal currents, dominance of longshore current direction, variable subsidence, and other factors.
One study showed atypical patterns of asymmetry for verbal production and spatial attention to be more common in left-handers than in right-handers [8].
Therefore, it is possible that, when both males and females are included, the patterns of asymmetry in chimpanzees' corticospinal system as well as its relationship with handedness might differ.
The absence of a distinct strand bias can also be explained by the recent inversion of single genes which homogenize general patterns of asymmetry [ 33, 34].
The consistency of the patterns of asymmetry across species pairs suggests that much of the asymmetry results from selection caused by the different habitat temperatures.
Differences in other aspects of the environment, such as salinity, hydrostatic pressure, pH, oxygen, and nutrient source, could cause patterns of asymmetry that are unrelated to temperature and therefore different in different mesophile thermophile pairs.
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While the sources of asymmetries are not addressed directly in the present paper, the documented patterns of asymmetries tend to hint on the presence of market power within the food supply chains.
We report on the patterns of asymmetries of various MRI-derived cortical phenotypes, namely cortical thickness (CT), cortical surface area (CSA), cortical volume (CV) and sulcal depth (SULC), as well as on their cross-relationships.
In fish genomes we find other patterns of asymmetries than in mammals.
The degree and pattern of asymmetry is estimated by tracking the bi-lateral lip points.
A distinct difference in form between the ovens in the east and west follow a pattern of asymmetry that manifests at multiple levels across the mortuary landscape.
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