Forests
can be both sources and sinks of volatile organic compounds
to the atmosphere. The role that forests play in controlling organic
acid concentrations remains poorly understood with multiple model-measurement
comparisons reporting missing sources of formic acid. We conducted
seasonal measurements of concentrations and eddy covariance fluxes
of oxidized volatile organic compounds over a ponderosa pine forest
in Colorado in 2016. Diel concentration profiles show mid-day maxima,
consistent with previous studies. We observed persistent but variable
upward fluxes of formic, propionic, methacrylic, and butyric acids
from the pine forest during all seasons. Formic acid concentrations
and fluxes were ∼10 times higher than the other organic acids
with daytime exchange velocities on the order of 4–6 cm s–1. The other organic acids had similar exchange velocities
as formic acid in the warmer seasons and much smaller exchange velocities
in the colder seasons. The upward fluxes for all organic acids increased
exponentially with temperature. The observed net upward flux demonstrated
that dry deposition was smaller than ecosystem sources of the organic
acids. Primary emissions from soil and pine trees were small, in contrast
to estimates of in-canopy chemistry. Our study points to an underestimated
ecosystem source of organic acids (e.g., in-canopy chemistry of large
or multifunctional terpenoids), an overestimated dry deposition sink
(potentially due to the arid environment), and/or an unresolved sink
of organic acids in the upper boundary layer. Forests are potentially
large sources of atmospheric organic acids in warmer seasons but further
investigation into dry deposition mechanisms and in-canopy chemistry
is warranted.