In order to determine the effect of feeding glucose water on breastfeeding newborns, we randomly distributed 180 normal newborns into two groups: a glucose water group (GW), fed 5% glucose solution during the first 3 days of life in addition to being breastfed; and an exclusively breastfed nonglucose water group (NGW). The following data were evaluated: weight at 6, 12, 24, 48, and 72 hours of life; temperature during the first 72 hours of life; serum glucose level at 6, 12, 24, and 48 hours; total duration of breastfeeding and age at introduction of infant formulas. In the NGW, there was a greater weight loss at 48 hours but not at 72 hours, temperatures higher than 37.5 degrees C were more frequent, and the mean serum glucose levels at 6, 12, and 24 hours were lower. This group also had more serum glucose level determinations under 2.2 mmol/l (40 mg/dL). However, no infants exhibited hypoglycemic symptoms. Infants in the GW received twice as many formulas during the first month and had a shorter duration of any breastfeeding. Our results suggest that the suppression of feedings with glucose water in the first days of life increases the probability of successful breastfeeding. However, infants who do not receive glucose water in the first few days of life may require greater supervision and close monitoring of blood glucose and body temperature, particularly in the first 24 hours of life.

Mesquite beans (Prosopis juliflora) consisted of pericarp, hulls and kernels. With the exception of kernels, composition of beans and their fractions were protein, lo-IS%; fat, 2-3%; crude fiber, 20-30%; sucrose, 21%; reducing sugars, 2-6%. Kernels contained 38% protein, 3% fat and 9% crude fiber. Bean trypsin inhibitor content was 1.4 TIU/mg. Bean protein isoelectric point was pH 5. Mesquite protein concentrate and isolate were prepared, however, by increasing solubility at the extraction pH (pH 10) with NaCl and decreasing it at the isoelectric point with (NH&S04. First and second limiting amino acids for bean protein were threonine and isoleucine, respectively; the protein was high in total sulfur amino acids and tryptophan. Corrected PER was 1.4.

SUMMARY Radio‐frequency heating at 60 and 2450 MHz in conveyorized equipment was compared with conventional hot water treatment for pasteurization of small cured hams packed in Cryovac casings inside moulds. For lean 2‐lb hams, treatment time to reach the desired central temperature could be reduced to 1/3 by heating in a condenser field tunnel operating at 60 MHz, with substantial reduction of juice losses and a tendency to improve sensory quality compared with that obtained with hot water processing. Treatment time could be further reduced by roughly the same extent by processing at 2450 MHz, but product thickness had to be reduced to secure sufficient heat penetration. Temperature gradients end juice losses were comparable to those in hot water treatment. At 2450 MHz in particular, but also at 60 MHz, bacterial surface counts were considerably higher than in the controls, suggesting the need for higher final surface temperature or supplementary heat treatment, which will lower the differences in processing time and juice loss between methods.

SUMMARY— The following variables were determined at equilibrium between fish muscle and brine, all as functions of the salt concentration in the brine: salt concentration in the muscle, based on the volume of the muscle; salt concentration in the tissue water of the muscle; distribution coefficient of salt between muscle volume and brine; distribution coefficient of salt between muscle tissue water and brine. Secondary variables which further described the salting equilibria were also found as functions of salt concentration in the brine as follows, all based on unit weight of non‐salt solids in the salted muscle: weight of salt (S/NSS), weight of water (W/NSS), and volume (V/NSS). The salt concentration based on the muscle volume was found to increase continually with increasing brine concentration, as did the salt concentration in the tissue water and the salt content expressed as S/NSS. The distribution coefficient based on the muscle volume and the water and volume contents (W/NSS) and (V/NSS) were found to increase at first, pass through a maximum, and then decrease, all with increasing brine concentration. Within the limits of experimental error, the salt concentration in the tissue water was found to equal the salt concentration in the brine, so that the distribution coefficient calculated on this basis was always equal to unity and was independent of the salt concentration in the brine. The volume per unit weight of non‐salt solids (V/NSS) was found to be a direct linear function of the water content per weight of non‐salt solids (W/NSS) at all temperatures studied. Little difference was found between the equilibrium salting variables when salting was carried out at 5 and at 25°C; on the other hand, possibly due to “cooking” or heat denaturation of the muscle with consequent loss of water at that temperature, all variables were considerably lower when salting was carried out at 37°C. The “mean molar activity coefficient” of sodium chloride in fish muscle was determined as a function of salt concentration in the muscle. It was found to be always greater, and to vary more sharply with salt concentration, than the corresponding activity coefficient of salt in aqueous solution.