A similar finding was reported in spatial modeling of malaria in Bangladesh, where environmental variables described a large proportion of spatial variation in P. falciparum, but little of the P. vivax distribution.
Functional asymmetries between hemispheres have been reported in relation to spatial and temporal information processing.
Evidence for far transfer from instrumental music training has previously been reported in the areas of spatial, verbal, and mathematical performances, as well as general IQ, as described below.
In addition, surgical ablation of CC does not severely affect the general activity of goldfish [ 18, 23], and cerebellar involvement in spatial learning has been reported in goldfish [ 18].
Atypical asymmetries of spatial attention have been reported in children with attention deficit hyperactivity disorder (ADHD) and may be exacerbated by non-spatial factors such as attentional capacity.
Elevated concentrations of Potentially Toxic Elements (PTEs) in bulk sediment (Cu, Zn, Pb, Ni, Cr, Li, V, Fe, As, Se, and Mn) have been reported in surficial sediments and have relatively uniform spatial distributions.
Social constraints to individual exchanges between population spatial units have been reported in various gregarious ungulate species [ 1, 15].
The IZ is usually described as being in the middle region of the muscle belly [ 11], but more complex IZ spatial distibutions have been reported in muscles with unipennate or multipennate fibre arrangements (e.g., gastrocnemius and soleus) [ 12- 14].
Similarly, a more negative judgement of ambiguous spatial stimuli has been reported in response to acute induction of a negative state through illumination of test apparatus with bright light, although this occurred only in rats that had been trained in low lighting levels then tested in bright light (Burman et al., 2009).
Indeed, after ablating neurogenesis, spatial memory deficits have been reported in some studies [18], [19] but not in others [20] [25].
