Mobilization of natural nitrate (NO 3 -) deposits in the subsoil by irrigation water in arid and semiarid regions has the potential to produce large groundwater NO 3 -concentrations. The use of isotopes to distinguish between natural and anthropogenic NO 3 -sources in these settings could be complicated by the wide range in δ 15 N values of natural NO 3 -. An ∼10 000 year record of paleorecharge from the regionally extensive High Plains aquifer indicates that δ 15 N values for NO 3 -derived from natural sources ranged from 1.3 to 12.3‰ and increased systematically from the northern to the southern High Plains. This collective range in δ 15 N values spans the range that might be interpreted as evidence for fertilizer and animal-waste sources of NO 3 -; however, the δ 15 N values for NO 3 -in modern recharge (<50 years) under irrigated fields were, for the most part, distinctly different from those of paleorecharge when viewed in the overall regional context. An inverse relation was observed between the δ 15 N[NO 3 -] values and the NO 3 -/Cl -ratios in paleorecharge that is qualitatively consistent with fractionating losses of N increasing from north to south in the High Plains. N and O isotope data for NO 3 -are consistent with both NH 3 volatilization and denitrification, having contributed to fractionating losses of N prior to recharge. The relative importance of different isotope fractionating processes may be influenced by regional climate patterns as well as by local variation in soils, vegetation, topography, and moisture conditions.