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The average PAH distribution pattern for forest soils is shown in Table 8 and in Figure 6.
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Although significant values can indicate historical population expansion, the multimodal pattern for the forest elephant groups suggests that these populations encompass several subgroups as indicated in the networks.
Relative to 1-m stheks, the vertical SOC distribution confirmed global patterns reported for forest soils: ~ 50% of SOC was stored in the upper 20 cm, and ~ 55 65% in the upper 30 cm of soil.
Kitagawa et al. (2014) analysed the spatial pattern of forest structure for a 306-ha water catchment in a Japanese mountainous area, and they pointed out that local above-ground biomass could be explained through the topographical features of the site.
This study analyses the spatio-temporal pattern of forest cover dynamics for three decades in Falgore Game Reserve in Kano, Nigeria.
(For restoring the normal pattern of forest growth the total amount of wood cut by a given age was added to reported wood stock at this age).
As expected, the deepest subdivision detected in our phylogenies corresponded to the basal 'F' and 'S' mtDNA clades (Debruyne 2005), and the mtDNA pattern was nonmonophyletic for forest and savanna elephant species (Debruyne 2005; Roca et al. 2005; Lei et al. 2009).
This study provides a way to comprehensively analyze habitat fragmentation and functional patterns for local forest conservation.
Good reconstructions of invasion patterns for other forest diseases have been generated (reviewed in Garbelotto 2008; see also Dutech et al. 2012), but this is the first detailed reconstruction of an emergent exotic forest diseases in a time-frame of <20 years.
The present study sought to establish relationships between the spatial pattern of forest cover and these forests' accessibility – either on foot or by bike – for short walks.
The pattern of forest dynamics was also tested against available data on alternative drivers of forest change that had a spatial resolution relevant for the scale of our analysis.
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