Interaction between visually impaired students and their nonhandicapped classmates is an expected outcome of mainstreaming. The study reported on in this article tested this premise using the Interaction Observation Schedule for systematic observation and recording of the interactions of visually impaired students and their nonhandicapped classmates. Teachers’ responses to the Teacher Questionnaire were also used. Both the systematic observations and the teachers’ responses indicated that visually impaired students interact less frequently than their nonhandicapped classmates. These findings suggest that encouragement of interaction between visually impaired students and their classmates will have to be a more explicit undertaking than has been generally realized.
Ractopamine hydrochloride (RAC) is a beta-agonist approved by the U.S. Food and Drug Administration (FDA) as a medicated feed ingredient for cattle during the final days of finishing to improve feed efficiency and growth. Maximum residue limits and U.S. FDA residue tolerances for target tissues have defined management practices around RAC usage in the U.S. However, many countries have adopted zero tolerance policies and testing of off-target tissues, presenting a major challenge for international export. Therefore, the objective this study was to determine the necessary withdrawal time among cattle group-fed RAC to achieve residue concentrations below tolerance levels in muscle and off-target tissues. Specifically, both total and parent RAC residues were quantified in muscle, adipose tissue, rendered tallow, and large intestines from animals group-fed RAC and subjected to withdrawal 2, 4, or 7 days before harvest. Ractopamine (parent and total) residues were below the assay limit of detection (< 0.12 ng/g) in all muscle and adipose tissue samples from animals in control groups (no RAC). However, RAC residues were detectable, but below the limit of quantitation, in 40% of tallow and 17% of large intestine samples from control animals. As expected, mean RAC residue concentrations in muscle, adipose tissue, and large intestine samples decreased (P < 0.05) as the RAC withdrawal duration (days) was extended. Irrespective of RAC withdrawal duration, mean parent RAC residue concentrations in muscle, adipose tissue, and large intestine ranged from 0.33 to 0.76 ng/g, 0.16 to 0.26 ng/g, 3.97 to 7.44 ng/g, respectively and all tallow samples were > 0.14 ng/g (detectable but below the limit of quantitation). Results of this study provide a baseline for the development of management protocol recommendations associated with withdrawal following group-feeding of RAC to beef cattle in countries that allow RAC use and intend to export to global markets which may be subject to zero tolerance policies and off-target tissue testing.
ObjectivesDue to developing meat trade issues associated with use of the β-agonist ractopamine hydrochloride (RH) as a growth-promoting agent in livestock production, this project was developed to provide recommendations of best practices to beef cattle producers in the United States who intend to export to China. This study is critically important in better understanding the bioaccumulation and depletion of RH in live animals, and how this may relate to depletion in differing tissues on animal harvest.This study was designed to determine dose response and depletion curves in the lower gastrointestinal (GI) tract of fistulated (i.e., cannulated- both rumen and duodenal) steers either receiving or not receiving ractopamine hydrochloride as part of the daily ration. There were originally five steers in this study, but due to performance challenges and scarring issues, one animal was removed from the study for a total of four test subjects.Materials and MethodsIn the dose and depletion study, four steers (n = 2 not receiving RH and n = 2 receiving RH at the approved dosage) were assessed from –3 d (still receiving RH if on the RH treatment) to 13 d post-withdrawal to determine the amount of RH present and length of time required for RH to clear the GI tract should a contamination event of low levels occur. Residues were quantified using liquid chromatography mass spectrometry (LC-MS).ResultsFor the dose and depletion study, RH residues were quantified in rumen fluids, rumen solids, fecal material, and duodenal fluids. Overall, the RH present in the two control steers (which did not receive RH) declined from approximately 30 ppb in all matrices 3 d before withdrawal to below the limit of quantitation at the end of withdrawal. Furthermore, samples tended to be below the limit of quantitation by Day 4 post-withdrawal. The steers that received RH also exhibited a decline of RH throughout the withdrawal period for all matrices (e.g., 5800 ppb in rumen fluids at day –3 versus 1.81 ppb 13 d post-withdrawal).ConclusionThe dose and depletion study results suggest that RH declines rapidly in the lower GI of beef cattle, with levels below detection by day four. There are events in which RH declines and then spikes, so further research may be necessary to determine why this rapid increase occurs.
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