Boundary critical behavior at m-axial Lifshitz points for a boundary plane parallel to the modulation axes

The critical behavior of semi-infinite $d$-dimensional systems with $n$-component order parameter $\bm{\phi}$ and short-range interactions is investigated at an $m$-axial bulk Lifshitz point whose wave-vector instability is isotropic in an $m$-dimensional subspace of $\mathbb{R}^d$. The associated $m$ modulation axes are presumed to be parallel to the surface, where $0\le m\le d-1$. An appropriate semi-infinite $|\bm{\phi}|^4$ model representing the corresponding universality classes of surface critical behavior is introduced. It is shown that the usual O(n) symmetric boundary term $\propto \bm{\phi}^2$ of the Hamiltonian must be supplemented by one of the form $\mathring{\lambda} \sum_{\alpha=1}^m(\partial\bm{\phi}/\partial x_\alpha)^2$ involving a dimensionless (renormalized) coupling constant $\lambda$. The implied boundary conditions are given, and the general form of the field-theoretic renormalization of the model below the upper critical dimension $d^*(m)=4+{m}/{2}$ is clarified. Fixed points describing the ordinary, special, and extraordinary transitions are identified and shown to be located at a nontrivial value $\lambda^*$ if $\epsilon\equiv d^*(m)-d>0$. The surface critical exponents of the ordinary transition are determined to second order in $\epsilon$. Extrapolations of these $\epsilon$ expansions yield values of these exponents for $d=3$ in good agreement with recent Monte Carlo results for the case of a uniaxial ($m=1$) Lifshitz point. The scaling dimension of the surface energy density is shown to be given exactly by $d+m (\theta-1)$, where $\theta=\nu_{l4}/\nu_{l2}$ is the anisotropy exponent.Comment: revtex4, 31 pages with eps-files for figures, uses texdraw to generate some graphs; to appear in PRB; v2: some references and additional remarks added, labeling in figure 1 and some typos correcte

Effects of Cooking in Solutions of Varying pH on the Dietary Fiber Components of Vegetables

To study the effect of pH on dietary fiber components of vegetables, beans, cauliflower, potatoes, peas and corn were cooked in buffers of pH 2, 4, 6, and 10. Water-soluble pectin and hemicellulose, water-insoluble pectin and hemicellulose, cellulose and lignin were quantitated in raw, cooked vegetables and cooking medium. Tenderness and pH of raw and cooked vegetables were determined. Texture varied with cooking medium. Cooked vegetables were most firm at pH 4 and softest at pH 10. Dietary components found in cooking medium reflected these textural changes. Vegetables which showed greater pH effects exhibited greater changes in fiber components.Peer Reviewedhttp://deepblue.lib.umich.edu/bitstream/2027.42/73821/1/j.1365-2621.1984.tb13237.x.pd

Can forest management based on natural disturbances maintain ecological resilience?

Given the increasingly global stresses on forests, many ecologists argue that managers must maintain ecological resilience: the capacity of ecosystems to absorb disturbances without undergoing fundamental change. In this review we ask: Can the emerging paradigm of natural-disturbance-based management (NDBM) maintain ecological resilience in managed forests? Applying resilience theory requires careful articulation of the ecosystem state under consideration, the disturbances and stresses that affect the persistence of possible alternative states, and the spatial and temporal scales of management relevance. Implementing NDBM while maintaining resilience means recognizing that (i) biodiversity is important for long-term ecosystem persistence, (ii) natural disturbances play a critical role as a generator of structural and compositional heterogeneity at multiple scales, and (iii) traditional management tends to produce forests more homogeneous than those disturbed naturally and increases the likelihood of unexpected catastrophic change by constraining variation of key environmental processes. NDBM may maintain resilience if silvicultural strategies retain the structures and processes that perpetuate desired states while reducing those that enhance resilience of undesirable states. Such strategies require an understanding of harvesting impacts on slow ecosystem processes, such as seed-bank or nutrient dynamics, which in the long term can lead to ecological surprises by altering the forest's capacity to reorganize after disturbance