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To obtain more information on some applications from population matrix models in ecological and evolutionary studies see [15] and the references therein.
The likelihood functions L E and L V are defined by the infinite product of Eq. (7) for the elastic and Newtonian viscous matrix models in Eqs.
Thus, these four matched Q matrix models balance the strengths and weaknesses of the single Q matrix models in different ways (triangulation process) and, furthermore, they provide, besides the single Q matrix models, additional models for specifying the best proxy for apprentices' real cognitive processes while solving the tasks.
Despite the widespread use of matrix models in ecology and conservation, studies evaluating alternative sampling designs remain limited.
Of these 68 studies, however, we were only able to determine the number of plants that had been used to parameterize the matrix models in 52 (Table 1).
However, the potential for sampling variance to bias estimates of λ has yet to be investigated for matrix models in which organisms are capable of regressing into smaller size classes.
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We propose a new templated matrix model in the present work.
The method is based on the discrete fracture and matrix model, in which fractures are represented as two-dimensional objects in a three-dimensional porous matrix.
To directly assess how ECM composition regulates this process, we used a nested 3D matrix model in which cell-populated collagen buttons were embedded in cell-free collagen or fibrin matrices.
Liu, et al. [41, 42, 43], proposed a shape control matrix model, a dynamic matrix model and a mechanism-intelligence collaboration matrix model in turn based on the relation between the shape control means and the shape standard patterns.
It was speculated that there was more matrix modeling in bilayered substitutes to help ECs with branch formation).
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