Metabolic routing of dietary nutrients in birds: Effects of dietary lipid concentration on δ\u3csup\u3e13\u3c/sup\u3eC of depot fat and its ecological implications

During migration, many songbirds eat primarily fruit while depositing fat. Given that some fruits contain mostly carbohydrate and others contain mostly lipid, the ability of birds to fatten may depend on the macronutrient composition of the fruit. Stable isotopes of carbon may be useful in determining the source of nutrients used for synthesizing fat, because the enzyme that regulates the transfer of carbon skeletons from carbohydrate into fat synthesis has a higher affinity for 12C than for 13C, whereas dietary lipids can be directly incorporated into animal fat. Thus, fat stores of animals that are synthesized directly from dietary lipid should have isotopic signatures similar to dietary lipid, whereas biosynthesis of fats from dietary carbohydrates should produce changes in isotopic signatures. We tested these predictions by manipulating the concentrations and isotopic signatures of macronutrients in diets fed to Yellow-rumped Warblers (Dendroica coronata). The δ13C of depot fat in birds fed high-lipid diets was similar to that of dietary lipid, whereas δ13C of depot fat in birds fed low-lipid diets indicated that a combination of dietary lipid and carbohydrate were used to synthesize depot fat. Models that incorporated 8‰ discrimination between dietary carbohydrate and depot fat consistently estimated the proportion of dietary lipid and carbohydrate routed into depot fat. Stable-isotope analysis of macronutrients in the diet of wild birds combined with estimates of the effects of diet composition on the isotopic signature of depot fat in birds offer a method to identify the relative importance of nutritional resources used by songbirds to deposit fat. © The American Ornithologists\u27 Union, 2007

Stable isotopes in breath, blood, feces and feathers can indicate intra-individual changes in the diet of migratory songbirds

We used stable isotopes of C in breath, blood, feces and feathers to identify intra-individual changes in diet and the timescale of diet changes in free-living songbirds at a stopover site. Because accurate interpretation of differences between the δ13C of breath, plasma, and red blood cells (RBCs) relative to diet requires knowing the turnover rate of C within them, we determined the rate of change of C in breath, plasma and RBCs for yellow-rumped warblers (Dendroica coronata). Half-lives of C in breath, plasma, and RBCs were 4.4 ± 2.1 h, 24.8 ± 12.3 h and 10.9 ± 3.2 days, respectively, for yellow-rumped warblers. δ13C of breath, plasma, RBCs and feces from wild-caught golden-crowned kinglets (Regulus satrapa), ruby-crowned kinglets (R. calendula) and gray catbirds (Dumetella carolinensis) indicated that they had maintained an isotopically consistent diet for an extended period of time. However, δ13C of breath and plasma indicated that white-throated sparrows (Zonotrichia albicollis) had recently expanded their diet to include a C4 dietary component. Likewise, δ13C of breath, plasma, RBCs and feces indicated that some wild-caught yellow-rumped warblers had consumed foods with a more enriched protein signature prior to their arrival on Block Island, and since arrival, they had consumed mostly northern bayberry (Myrica pensylvanica). Therefore, comparisons of the δ13C of breath, plasma, RBCs, feces and feathers from individual songbirds can indicate changes in diet and provide an estimate of the timescale of the diet change. © Springer-Verlag 2004

Hydrogen and oxygen isotope values in hydrogen peroxide

Hydrogen peroxide (H 2 O 2 ) is a widely used oxidizer with many commercial applications; unfortunately, it also has terrorist-related uses. We analyzed 97 hydrogen peroxide solutions representing four grades purchased across the United States and in Mexico

Detection of metabolic fluxes of O and H atoms into intracellular water in mammalian cells.

Metabolic processes result in the release and exchange of H and O atoms from organic material as well as some inorganic salts and gases. These fluxes of H and O atoms into intracellular water result in an isotopic gradient that can be measured experimentally. Using isotope ratio mass spectroscopy, we revealed that slightly over 50% of the H and O atoms in the intracellular water of exponentially-growing cultured Rat-1 fibroblasts were isotopically distinct from growth medium water. We then employed infrared spectromicroscopy to detect in real time the flux of H atoms in these same cells. Importantly, both of these techniques indicate that the H and O fluxes are dependent on metabolic processes; cells that are in lag phase or are quiescent exhibit a much smaller flux. In addition, water extracted from the muscle tissue of rats contained a population of H and O atoms that were isotopically distinct from body water, consistent with the results obtained using the cultured Rat-1 fibroblasts. Together these data demonstrate that metabolic processes produce fluxes of H and O atoms into intracellular water, and that these fluxes can be detected and measured in both cultured mammalian cells and in mammalian tissue