We present one year of δD, δ18O, d-excess, and Δʹ17O data from monthly precipitation at a Caribbean coastal site in Panama and from tap waters across the country to constrain geographic, climate, and moisture source controls on isotopic variability and better understand the sources and mechanisms of precipitation in Central America, a region facing significant modifications to the annual rainfall cycle due to climate change. Monthly precipitation δD ranged from –52.2 to +14.3 ‰, δ18O from –7.6 to +0.4 ‰, d-excess from +7.1 to +11.6 ‰, and Δ′17O from +11 to +29 per meg. Rainy season precipitation samples were found to have lower δD, δ18O, and d-excess due to Rayleigh distillation during the condensation and rainout of Pacific moisture over the central cordilleras, which results in decoupling between d-excess and Δ′17O. Outlier Δ′17O values during peak dry and rainy months may reflect seasonal changes in water vapor sourcing, from Caribbean to Pacific and/or locally recycled moisture, or may be a result of organic contamination. Tap water δD ranged from –82.3 to –14.3 ‰, δ18O from –11.6 to –2.4 ‰, d-excess from +4.3 to +12.2 ‰ and Δ′17O from –2 to +84 per meg. Tap water δD and δ18O values increase eastward due to lower orographic effects and Pacific and locally recycled moisture contributions to rainfall and greater secondary evaporation. Tap water d-excess and Δ′17O values are also de-coupled but lack clear spatial trends and controls. The results of this study indicate the promise of adding Δ′17O to the isotopic toolkit in tropical mountainous regions with complicated water cycling dynamics and provide a baseline for future triple oxygen isotope investigations.
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