Genetic evidence suggests that, in addition to its role in meristem maintenance, STM also contributes to organ separation in the meristem, in conjunction with other boundary expressed genes, such as CUC, KNAT6, JLO and LOF genes (Lee et al., 2009; Aida et al., 2002; Belles-Boix et al., 2006; Spinelli et al., 2011; Borghi et al., 2007; Aida et al., 1999).
In addition, there are other boundary conditions for which the solutions converge to zero at infinite distances from the seawater: {b}_z=P {e}^{-kappa z}kern1.5em left(0le zright), kern0.5em {b}_z=Q {e}^{kappa left z+hright)}kern1.5em left zle -hright).
One may wonder whether such artificial mechanical perturbations could induce the expression of all meristematic genes, and in particular other boundary-expressed genes, as a non-specific stress response.
The same result holds for the other boundary curves in this system.
The implementation of various other boundary conditions in triangular differential quadrature analysis is also discussed and the sensitivity of solution to the implementation of corner conditions in vibrational analysis is highlighted.
In the event of having other boundary conditions, using extensively large domains is necessary to acquire meaningful results.
In this paper we consider other boundary conditions that imply that the operator is not a Volterra one even in the case when all are Volterra operators.
If with the algorithm we have not found a solution until m has equality to one of the boundary points of K, put the other boundary point in m.
The other boundary conditions in (2.30) are imposed on the first and the last rows of the modified Ai-1matrix on the left side of the equal sign in (2.29).
If R 0 > 1, then Eq. (3) has two equilibria in the first quadrant, which are E 0 and E ∗ = ( I ∗, R ∗ ), where I ∗, R ∗ > 0. Proof Clearly, Eq. (3) always has an equilibrium E 0 = ( 0, 0 ), and it has no other boundary equilibrium in the first quadrant from the second equation of (3).
