Effects of alkaline hydrogen peroxide treatment of cotton and wheat straw on cellulose crystallinity and on composition and site and extent of disappearance of wheat straw cell wall phenolics and monosaccharides by sheep

Effects of alkaline hydrogen peroxide (AHP) treatment on cellulose crystallinity and cell wall phenolic monomer and monosaccharide composition were measured using cotton and wheat straw (WS). Two WS treatments were used in this study, Type I WS, for which pH is not regulated during AHP treatment, and Type II WS, for which pH is regulated at 11.5 +/- .2 during AHP treatment. Wheat straw had a lower degree of cellulose crystallinity than cotton, but no differences occurred between treated and untreated substrates. Alkali-labile and nitrobenzene-extractable phenolic monomer concentrations were generally lower for Type I and Type II WS compared with untreated WS. Concentrations of glucose were higher and xylose and arabinose lower in Types I and II WS than in untreated WS. Disappearance of alkali-labile phenolic monomers and cell wall monosaccharides by wethers fed diets containing Type I (Exp. 1) or Type II (Exp. 2) AHP-treated WS were determined. Apparent digestibility of glucose and xylose before the duodenum, and of glucose, xylose and arabinose in the total tract, was greatest (P less than .05) when sheep were fed AHP-treated WS diets in both experiments. In Exp. 2, disappearance of alkali-labile phenolic monomers was greatest (P less than .05) before the duodenum and in the total tract when sheep were fed AHP-treated WS diets. Treatment of WS with AHP modified cell wall composition and increased cell wall monosaccharide digestion by sheep.     

Determination of methomyl in rape seeds,oils and meals

Methomyl added to rape seeds, oils or meals was detected by a thin-layer chromatographic-enzyme inhibition technique. The limit of detection in the presence of oil or meal extractive was 20 mg or 0.01 mg/kg. The amounts of methomyl recovered from oils and meals fortified at 0.01 to 20 mg/kg were comparable to the standard. When stored at 4 °C, methomyl in oil or meals, or in chloroform extracts, was stable for at least 10 and 21 days, respectively. No degradation was observed when methomyl was heated in ethanol at 72 °C for 2 h. Methomyl and its oxime were also detected with either iodo- or chloroplatinate reagent after t.l.c. The detection limits were approximately 600 mg for methomyl and 190 for the oxime.     

Effects of aflatoxin, deoxynivalenol, and their combinations in the diets of growing pigs

In 2 studies, the effects of dietary aflatoxin (AF) and deoxynivalenol (DON) were evaluated in growing crossbred barrows. The first study consisted of 4 treatments of 5 barrows each (6 weeks old) at dosages of 0 mg of DON and AF (control), 2.5 mg of DON/kg of feed, 0.75 mg of AF/kg of feed, and 2.5 mg of DON + 0.75 mg of AF/kg of feed. Pigs were fed their respective diets for 21 days. Treatment with DON caused decreases in weight gains, but no other treatment-related differences could be attributed to diets. In a second study, the experimental design consisted of 4 treatments of 5 barrows each (6 weeks old) at dosages of 0 mg of DON and AF (control), 3 mg of DON/kg of feed, 3 mg of AF/kg of feed, and 3 mg of DON + 3 mg of AF/kg of feed fed ad libitum for 28 days. The pigs were observed twice daily for clinical signs, hematologic and serum biochemical measurements were made weekly, and body weights and feed consumption were determined weekly. Body weight gains were significantly depressed by the AF and the AF + DON treatments for days 7, 14, 21, and 28. Body weights and body weight gains were only slightly reduced in the DON treatment. Changes in serum enzymatic activities of alkaline phosphatase, aspartate transaminase, creatine kinase, and gamma-glutamyl transferase were noticed in pigs given treatments with AF alone and those given AF + DON.(ABSTRACT TRUNCATED AT 250 WORDS)     

Endocytosis of erythrocytes in vivo and particulate substances in vitro by feline neoplastic mast cells.

Clinical evidence for the phagocytic capability of neoplastic feline mast cells was provided by recognition of endocytosed erythrocytes in seven of 12 cytological smears of mast cell neoplasms, particularly in those cells collected from splenic tumors. The capability of these neoplastic mast cells to endocytose particulate substances was also studied in vitro. Evidence is presented that under cultural conditions, feline neoplastic mast cells are capable of endocytosing a variety of substances including polystyrene latex microspheres, zymosan particles, horse spleen ferritin, salmon sperm nuclei, horseradish peroxidase, and carbon particles.     

Effect of pre- and postweaning management system on the performance on Brahman crossbred feeder calves

During a 3-yr period (1986 through 1988), 117 calves (57 steers and 60 heifers) from the same genetic base and reared under four distinct preweaning management systems were weaned in the fall and transported from Uvalde, TX to El Reno, OK (800 km). Weaning weight and transportation shrink varied more from year to year than among preweaning treatments. Postweaning performance was not affected by preweaning treatment. After a 28- to 32-d receiving period the calves were blocked by sex and previous preweaning treatment, then randomly assigned within block to graze winter wheat forage (WHEAT) or dormant tall-grass native range (GRASS). The WHEAT group gained more (P less than .01) weight than the GRASS group during the winter (November to March), but when both groups were allowed to graze spring wheat pasture (March to June) the GRASS group gained more (P less than .01) weight than the WHEAT calves. During the subsequent finishing phase the GRASS calves were more (P less than .01) efficient than the WHEAT calves in converting DM to gain. Because cattle were slaughtered at the same degree of finish, no differences were noted in carcass characteristics among the pre- or postweaning treatments. Feeder calves exposed to a restrictive period of growth during the postweaning period gained weight more rapidly in a subsequent forage-based stockering system and were more efficient in a grain-based finishing system than nonrestricted calves.     

Evaluation of granulocyte transfusion in healthy neonatal pony foals

Granulocyte transfusions (GT), 0.98 X 10(9) neutrophils/kg of body weight, were performed on 7 healthy pony foals between 2 and 7 days old. The mean neutrophil count of the foals was significantly (P less than 0.05) greater than base line (4,830 +/- 1,260/microliter) 1 hour after GT (8,870 +/- 3,350/microliter) and was similar to base line by 15 to 18 hours after GT (6,550 +/- 2,310/microliter). Leukocyte concentrates (LC) used for GT were harvested from clinically normal adult horses by continuous-flow centrifugation leukapheresis (CL), 3 to 6 hours after hydrocortisone sodium succinate was administered to increase the blood neutrophil count. The mean neutrophil count of the LC used for GT was 68,050 +/- 13,990/microliter, and the mean LC volume was 377.4 +/- 79.2 ml (14.82 +/- 3.54 ml/kg). The mean time required to collect the LC used for GT was 232.1 +/- 73.4 minutes. Neutrophils from LC had significantly reduced in vitro stimulated migration to zymosan-activated serum, when compared with peripheral blood neutrophils of the donors (P less than 0.05). Neutrophil phagocytosis and bactericidal capacity were not significantly changed in LC. Mean neutrophil migration indices were not significantly different in foals after GT. Mild depression and transient diarrhea was noticed in 1 foal 30 minutes after the start of the GT. The donor of LC for this foal and 1 other donor experienced depression, piloerection, and muscle tremors during CL, indicating that complement had been activated. Problems were eliminated by the use of new disposable plastic materials for blood processing in each CL procedure.