Fifty years ago, GE Hutchinson defined the ecological niche as a hypervolume in n‐dimensional space with environmental variables as axes. Ecologists have recently developed renewed interest in the concept, and technological advances now allow us to use stable isotope analyses to quantify these niche dimensions. Analogously, we define the isotopic niche as an area (in δ‐space) with isotopic values (δ‐values) as coordinates. To make isotopic measurements comparable to other niche formulations, we propose transforming δ‐space to p‐space, where axes represent relative proportions of isotopically distinct resources incorporated into an animal's tissues. We illustrate the isotopic niche with two examples: the application of historic ecology to conservation biology and ontogenetic niche shifts. Sustaining renewed interest in the niche requires novel methods to measure the variables that define it. Stable isotope analyses are a natural, perhaps crucial, tool in contemporary studies of the ecological niche.

For decades, plant ecologists have used naturally occurring stable isotope ratios to disentangle ecological and physiological processes. The methodology can also become a very powerful tool in animal ecology. However, the application of the technique relies on assumptions that are not widely recognized and that have been rarely tested. The purpose of this communication is to identify these assumptions, to characterize the conditions in which they are not met, and to suggest the laboratory experiments that are needed to validate them. The ease with which isotopic data can be gathered and the growing popularity of the method are generating a large amount of data on the isotopic ecology of animals. The proper interpretation of these data demands that we identify the assumptions on which these inferences are based, and that we conduct comparative laboratory experiments to assess their validity.

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For decades, plant ecologists have used naturally occurring stable isotope ratios to disentangle ecological and physiological processes. The methodology can also become a very powerful tool in animal ecology. However, the application of the technique relies on assumptions that are not widely recognized and that have been rarely tested. The purpose of this communication is to identify these assumptions, to characterize the conditions in which they are not met, and to suggest the laboratory experiments that are needed to validate them. The ease with which isotopic data can be gathered and the growing popularity of the method are generating a large amount of data on the isotopic ecology of animals. The proper interpretation of these data demands that we identify the assumptions on which these inferences are based, and that we conduct comparative laboratory experiments to assess their validity.

The use of stable isotopes to infer diet requires quantifying the relationship between diet and tissues and, in particular, knowing of how quickly isotopes turnover in different tissues and how isotopic concentrations of different food components change (discriminate) when incorporated into consumer tissues. We used feeding trials with wild-caught yellow-rumped warblers (Dendroica coronata) to determine delta15N and delta13C turnover rates for blood, delta15N and delta13C diet-tissue discrimination factors, and diet-tissue relationships for blood and feathers. After 3 weeks on a common diet, 36 warblers were assigned to one of four diets differing in the relative proportion of fruit and insects. Plasma half-life estimates ranged from 0.4 to 0.7 days for delta13C and from 0.5 to 1.7 days for delta15N . Half-life did not differ among diets. Whole blood half-life for delta13C ranged from 3.9 to 6.1 days. Yellow-rumped warbler tissues were enriched relative to diet by 1.7-3.6% for nitrogen isotopes and by -1.2 to 4.3% for carbon isotopes, depending on tissue and diet. Consistent with previous studies, feathers were the most enriched and whole blood and plasma were the least enriched or, in the case of carbon, slightly depleted relative to diet. In general, tissues were more enriched relative to diet for birds on diets with high percentages of insects. For all tissues, carbon and nitrogen isotope discrimination factors increased with carbon and nitrogen concentrations of diets. The isotopic signature of plasma increased linearly with the sum of the isotopic signature of the diet and the discrimination factor. Because the isotopic signature of tissues depends on both elemental concentration and isotopic signature of the diet, attempts to reconstruct diet from stable isotope signatures require use of mixing models that incorporate elemental concentration.