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Stones were weighed after each fragmentation cycle and the percent weight lost was determined.
Number of cells in each fragmentation class for all selected zones in the study area (delineated in Fig. 5).
The mean canopy height difference between samples in each fragmentation class was determined using an analysis of variance ANOVA for all sample points.
A set 5000 points located randomly within the LiDAR footprints in Mai Ndombe were selected to assess canopy height and estimated AGB within each fragmentation class produced with varying edge distances.
While all edge distances showed significant differences, only an edge distance of 300 m produced significantly different differences of AGB between each fragmentation class pair (Mann Whitney p ≪ 0.005) (Fig. 7).
A Tukey honest significant difference and Mann–Whitney pairwise tests for non-parametric data were performed to determine a significant of difference in mean canopy height and biomass between each fragmentation category pair.
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One is fragmentation.
By modeling the compound fragmentation as a tree, we make the implicit assumption that each fragment in the fragmentation spectrum is generated by a single fragmentation pathway.
Proteome Discoverer 1.3 software was used to extract the peak intensity of each expected iTRAQ reporter ion from each analyzed fragmentation spectrum.
Counts of cells for each selected fragmentation index class; from left in both rows: edge, perforated, and interior.
For each experimental fragmentation spectrum, a report is generated, which includes detailed information on the matching and annotation.
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