Three experiments were performed investigating bovine enteric methane (CH) production inhibition using a proprietary kelp blend product (PKBP) containing a halogenated methane analog (i.e., bromoform). Calves were fed a corn-silage basal diet top-dressed with the assigned treatment, with rations provided at 1.5 × NE in Experiments 1 and 2 ( = 12 and 6 steers, respectively) and ad libitum in Experiment 3 ( = 9 steers). In Experiment 1, we evaluated bromoform's potency in decreasing CH. Dry matter intake (DMI) was not affected by treatment ( ≥ 0.11; 0 vs. 52.5 ± 10.5 ppm bromoform), whereas bromoform supplementation decreased CH ( < 0.01). In Experiments 2 and 3, treatments were 0, 9.5 ± 1.5, or 20 ± 3 ppm bromoform. In Experiment 2, we examined CH recovery following bromoform removal from the ration. Bromoform treatments were fed on d1, but not the subsequent 8 d, to investigate residual effects. On d1, CH was below limits of detection for 20 ppm bromoform inclusion. Across days, a cubic response ( < 0.01) was observed with 20 ppm bromoform inclusion, but not with 0 and 9.5 ppm inclusion levels. Experiment 3 (30 d finishing trial) tested bromoform effects on feeder calves. DMI ( = 0.53), average daily gain ( = 0.55), and gain:feed ( = 0.82) were not influenced by bromoform inclusion. Bromoform residues were undetectable in liver, kidney, adipose, and muscle samples collected at harvest. These experiments demonstrated that cattle fed PKBP experience short-term reductions in CH without tissue accumulation of bromoform and without evidence of effects on animal growth or feed consumption.
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http://dx.doi.org/10.3390/ani14162411 | DOI Listing |
Animals (Basel)
August 2024
Department of Animal and Food Sciences, University of Kentucky, Lexington, KY 40546, USA.
Three experiments were performed investigating bovine enteric methane (CH) production inhibition using a proprietary kelp blend product (PKBP) containing a halogenated methane analog (i.e., bromoform).
View Article and Find Full Text PDFWater Environ Res
November 2012
Environment and Industrial Safety Division, Indira Gandhi Centre for Atomic Research, Kalpakkam, India.
Formation character of brominated-trihalomethanes (Br-THMs) in chlorinated seawater and its dependence on applied chlorine dose, reaction time, and temperature were investigated in the laboratory. Seawater was collected from the east coast of India and a chlorine dose of 1, 3, 5, and 10 ppm was each applied at a temperature of 20, 30, and 40 degrees C to investigate the yield and kinetics of Br-THMs formation. Qualitative and quantitative estimation of THM formation at various intervals of time ranging from 5 min to 168 h was determined by a gas chromatograph equipped with an electron capture detector (GC-ECD).
View Article and Find Full Text PDFEnviron Sci Pollut Res Int
March 2010
Department of Health Risk Management, China Medical University, Taichung, 40402, Taiwan.
Introduction: The pyrolytic method was employed to recycle metals and brominated compounds blended into printed circuit boards (PCBs).
Methods: PCBs were crushed into pieces 4.0-4.
J Toxicol Environ Health A
February 2005
TOXHUM (Groupe de recherche en toxicologie humaine), Département de Santé Environnementale et Santé au Travail, Université de Montréal, Montréal, Québec, Canada.
The aim of this study was to investigate the in vitro metabolism of trihalomethanes (THMs) in the presence of trichloroacetic acid (TCA), dichloracetic acid (DCA), monochloroacetic acid (MCA), and 4-methylpyrazole (4-MP) using liver microsomes from male Sprague-Dawley rats. Using the vial equilibration technique, initial experiments were carried out with starting concentrations of approximately 40 ppm THMs and 12-22 mM chloroacetic acids. The results indicated a mutual metabolic inhibition between THMs present as binary or quaternary mixtures.
View Article and Find Full Text PDFPhotochem Photobiol
April 2002
Structural Biology Research Group, Department of Biological Sciences, University of Calgary, Alberta, Canada.
The light-dependent reaction between N-acetyl-L-tryptophanamide (NATA) and chloroform has been examined using fluorescence, NMR and reverse phase chromatography. The emission of NATA in the presence of CHCl3 decreases at 360 nm and increases at longer wavelengths (approximately 480 nm) upon illumination with 280 nm light. The action spectrum for the formation of the 480 nm emitting product(s) has the same shape as the excitation spectra of the indole fluorophore in NATA.
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