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However, regression models of site productivity seldom explain much more than 50% of the variability due to the difficulty in measuring many of the environmental variables which affect tree growth, particularly variables associated with soil fertility.
Accordingly, this paper explores three main alternative models of site formation: anthropogenic disposal of materials into the lake, a geological relocation of the artifacts, and hunting or caching on lake-ice.
Models of Site Index for plantation species growing outside of New Zealand have also frequently found air temperature to be an important determinant of Site Index (Sharma et al. 2012), but rainfall is at least as important as air temperature in many drier regions (Mohamed et al. 2014; Sabatia and Burkhart 2014).
We fitted two models of site variation of ω, the non-synonymous to synonymous rate ratio (Table 1).
Six different models of site- and/or branch-specific ω ratios [ 73, 74] were optimised using Bayesian methods in PAML 4.2 [ 72].
raxml uses a likelihood-based tree-searching algorithm to find an optimal phylogeny using GTR-based models of site substitution – GTR + Γ models were used for these analyses.
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Details of the problematic issues in cancer drug discovery and screening methods using experimental mice or rats models of site-specific tumors have been recently reported [22, 44, 115 121].
Model M8, one the most conservative models of site-specific evolution was determined to be significantly more favoured in comparison to the neutral M7 model (p = 5 × 10-23; Table 1).
The ages of these tephra layers were estimated using the age model of Site U1427.
This inter-site correlation enables us to transfer the age model of Site U1424 to all deeper sites, including Site U1426.
Reactive transport modeling of site geochemistry and hydrology is a highly useful for the design of effective MMV plans for carbon storage.
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