As a part of the ChArMEx (Chemistry Aerosol Mediterranean Experiments) and ENVI-Med CyAr (Cyprus aerosols and gas precursors) programs, this study aims primarily at providing an improved understanding of the sources and the fate of volatile organic compounds (VOCs) in the Eastern Mediterranean. More than 60 VOCs, including biogenic species (isoprene and 8 monoterpenes) and oxygenated VOCs were measured during a 1-month intensive field campaign performed in March 2015 at the Cyprus Atmospheric Observatory (CAO), a regional background site in Cyprus. VOC measurements were conducted using complementary on-line and off-line techniques. Biogenic (B)VOCs were principally imputed to local sources and characterized by compound-specific daily cycles such as diurnal maximum for isoprene and nocturnal maximum for α,β-pinenes, in connection with the variability of emission sources. The simultaneous study of pinenes and isoprene temporal evolution and meteorological parameters has shown that BVOC emissions were mainly controlled by ambient temperature, precipitation and relative humidity. It was found that isoprene daytime emissions at CAO depended on temperature and solar radiation changes whereas nocturnal BVOC concentrations (e.g. from oak and pine forests) were more prone on the relative humidity and temperature changes. Significant changes in monoterpene mixing ratios occurred during and after rain. The second part of the study focused on new particle formation events (NPF) at CAO. BVOCs are known to potentially play a role in the growth as well as in the early stages of formation of new atmospheric particles. Based on observations of the particle size distribution performed with a differential mobility particle sizer (DMPS) and the total number concentrations of particles larger than 1 nm diameter measured by particle-size magnifier (PSM), NPF events were found on 14 out of 20 days of the field campaign. For all possible proxy parameters (meteorological parameters, calculated H 2 SO 4 and measured gaseous compounds) having a role in NPF, we present daily variations of different classes during nucleation events and non-event days. NPF can occur at various condensational sink (CS) values and both under polluted and clean atmospheric conditions. High H 2 SO 4 concentrations coupled with high BVOC concentrations seemed to be one of the most favorable conditions to observe NPF at CAO in March 2015. NPF event days were characterized by either (1) a predominant anthropogenic influence (high concentrations of anthropogenic source tracers observed), (2) a predominant biogenic influence (high BVOC concentrations coupled with low anthropogenic tracer concentrations), (3) a mixed influence (high BVOC concentrations coupled with high anthropogenic tracer concentrations) and (4) a marine influence (both low BVOC and anthropogenic concentrations). More pronounced NPF events were identified during mixed anthropogenic-biogenic conditions compared to the pure anthropogenic or biogenic ones, for the same levels of precursors. Analysis of specific NPF periods of the mixed influence type highlighted that BVOC interactions with anthropogenic compounds enhanced nucleation formation and growth of newly formed particles. During these days, the nucleation mode particles may be formed by the combination of high H 2 SO 4 and isoprene amounts, under favorable meteorological conditions (high temperature and solar radiation and low relative humidity) and low CS. During the daytime, growth of the newly formed particles, sulfate but also oxygen-like organic aerosol (OOA) mass contributions increased in the particle phase. High BVOC concentrations were observed during the night following NPF events, accompanied with an increase of the CS and of semi volatile OOA contribution, suggesting further BVOC contribution to aerosol nighttime growth by condensing onto pre-existing aerosols.