Carcass characteristics and meat quality of lambs fed high levels of spineless cactus in the diet

The objective was to evaluate the effect of increasing the dietary inclusion of spineless cactus (Nopalea cochenillifera Salm Dyck) on the carcass characteristics and meat quality of confined lambs. Thirty-two male Santa Inês lambs with an average age of 140 days and an initial body weight of 20.4 ± 2.60 kg were used in this study. The lambs were housed in individual stalls for 70 days and individually fed a ration with spineless cactus included at 0, 241, 519, or 753 g/kg of dry matter (DM). The lambs were slaughtered, and characteristics of the carcass and meat were recorded and analysed. Inclusion of spineless cactus had a quadratic effect on the bodyweight at slaughter and on the empty bodyweight of the lambs. The inclusion of 500 g/kg of spineless cactus provided the highest predicted cold carcass weight (16.03 kg). There was a quadratic effect of the inclusion of spineless cactus on the weight of meat cuts and leg composition of lambs. The inclusion of spineless cactus did not influence pH, tenderness, and water-retention capacity of the meat. However, the intramuscular fat content increased 1 mg for every 10 g/kg inclusion of spineless cactus in the diet. Quadratic effects were observed of the inclusion of spineless cactus on the weights of the liver, heart, rumen, blood, skin and internal fat of the lambs. Up to 500 g/kg of spineless cactus could be included in the diet of confined lambs

Counting BPS states on the Enriques Calabi-Yau

We study topological string amplitudes for the FHSV model using various techniques. This model has a type II realization involving a Calabi-Yau threefold with Enriques fibres, which we call the Enriques Calabi-Yau. By applying heterotic/type IIA duality, we compute the topological amplitudes in the fibre to all genera. It turns out that there are two different ways to do the computation that lead to topological couplings with different BPS content. One of them leads to the standard D0-D2 counting amplitudes, and from the other one we obtain information about bound states of D0-D4-D2 branes on the Enriques fibre. We also study the model using mirror symmetry and the holomorphic anomaly equations. We verify in this way the heterotic results for the D0-D2 generating functional for low genera and find closed expressions for the topological amplitudes on the total space in terms of modular forms, and up to genus four. This model turns out to be much simpler than the generic B-model and might be exactly solvable.Comment: 62 pages, v3: some results at genus 3 corrected, more typos correcte

Nonequilibrium wetting

When a nonequilibrium growing interface in the presence of a wall is considered a nonequilibrium wetting transition may take place. This transition can be studied trough Langevin equations or discrete growth models. In the first case, the Kardar-Parisi-Zhang equation, which defines a very robust universality class for nonequilibrium moving interfaces, with a soft-wall potential is considered. While in the second, microscopic models, in the corresponding universality class, with evaporation and deposition of particles in the presence of hard-wall are studied. Equilibrium wetting is related to a particular case of the problem, it corresponds to the Edwards-Wilkinson equation with a potential in the continuum approach or to the fulfillment of detailed balance in the microscopic models. In this review we present the analytical and numerical methods used to investigate the problem and the very rich behavior that is observed with them.Comment: Review, 36 pages, 16 figure