We report fallout radionuclide (FRN) and major/trace element (MTE) contributions to bulk atmospheric deposition in Hanover, NH USA (43.7022° N, 72.2896° W). Deposition of ⁷Be, ²¹⁰Pb and SO₄ covary [R²>0.4, n=461] but are discriminated by production sources, depositional mechanisms, meteorological controls, MTE associations, and seasonal biases. ⁷Be is dominated by rainout (78% of total deposition), recharged by long-range transport (+23% over mean, o.m.), influenced by stratosphere-troposphere-exchange (+9% o.m.) and solar activity (-2% per doubling of sunspot count). Correlation with particulate nitrogen (+9% per doubling of N) indicates ⁷Be affinity for biogenic aerosols. ²¹⁰Pb is dominated by dry+washout deposition (54% of total) and convective storms (+107% o.m), is depleted in marine moisture sources (-133% o.m.), correlated with S (+9% per doubling of S) and biased to autumn with Mn, Hg, and V (+7% o.m.). Coincident long-term declines in S and ²¹⁰Pb (-14%, -4% per year) suggest co-scavenging by PbSO₄. ⁷Be:²¹⁰Pb ratios increase asymptotically with precipitation through the dry-washout-rainout transition and recharge of ⁷Be. At the global scale, ⁷Be:²¹⁰Pb increases with precipitation for North American/European sites due to recharge of ⁷Be in mid-latitude storm belts [R²=0.64, n=31]. Conversely, ⁷Be:²¹⁰Pb is independent of precipitation for Southeast/East Asian sites where ⁷Be recharge is low [R²=0.01, n=40]. Globally, ⁷Be:²¹⁰Pb ratios in dry deposition reflect resuspended aerosols with mean age of ca. 200 days, contributing <5% of ²¹⁰Pb deposition. Different aerosol populations contributing to FRN deposition across spatial and temporal scales should emerge as a focus in terrestrial ⁷Be, ²¹⁰Pb and ¹⁰Be tracer applications.