With increasing concern over chemicals that are potential health hazards at low levels, determination of limits of detection have undergone considerable scrutiny. Most traditional detection limit estimators suffer from extensive statistical and/or conceptual limitations. In this paper, traditional detection limit estimators are described and critically evaluated. Using the terminology of Currie (1968), methods are categorized into decision limits versus detection limits. The methods are further categorized into single concentration design versus calibration design methodologies. While the single concentration design methods are useful for fixing ideas and clarifying definitions, they are shown to be extremely limited in practice since dependence of variability on concentration can neither be estimated or incorporated. Calibration-based detection limit estimators are described, compared and contrasted. Generalizations to non-constant variance, multiple future detection decisions and simultaneous control of Type I and II errors are provided. The various calibration-based methods are illustrated using real data and experimental design issues for detection limit studies discussed.