Nitrous oxide (N2O), a potent greenhouse gas, is produced disproportionately in marine oxygen deficient zones (ODZs). To quantify spatiotemporal variation in N2O cycling in an ODZ, we analyzed N2O concentration and isotopologues along a transect through the eastern tropical North Pacific (ETNP). At several stations along this transect, N2O concentrations reached a near surface maximum that exceeded prior measurements in this region, of up to 226.1 ± 20.5 nM at the coast. Above the σθ = 25.0 kg/m3 isopycnal, Keeling plot analysis revealed two sources to the near‐surface N2O maximum, with different δ15N2Oα and δ15N2Oβ values, but each with a site preference (SP) of 6‰–8‰. Given expected SPs for nitrification and denitrification, each of these sources could be comprised of 17%–26% nitrification (bacterial or archeal), and 74%–83% denitrification (or nitrifier‐denitrification). Below the σθ = 25.0 kg/m3 isopycnal, box model analysis indicated that the observed 46‰–50‰ SPs in the anoxic core of the ODZ cannot be reproduced in a steady state context without an SP for N2O production by denitrification, and may indicate instead a transient net consumption of N2O. Furthermore, time‐dependent model results indicated that while δ15N2Oα and δ18O‐N2O reflect both N2O production and consumption in the anoxic core of the ODZ, δ15N2Oβ predominantly reflects N2O sources. Finally, we infer that the high (N2O) observed at some stations derive from a set of conditions supporting high rates of N2O production that have not been previously encountered in this region.

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Our understanding of the biogeochemical cycling of monomethylmercury (MMHg) in the Arctic is incomplete because atmospheric sources and sinks of MMHg are still unclear. We sampled air in the Canadian Arctic marine boundary layer to quantify, for the first time, atmospheric concentrations of methylated Hg species (both MMHg and dimethylmercury (DMHg)), and, estimate the importance of atmospheric deposition as a source of MMHg to Arctic land- and sea-scapes. Overall atmospheric MMHg and DMHg concentrations (mean ± SD) were 2.9 ± 3.6 and 3.8 ± 3.1 (n = 37) pg m(-3), respectively. Concentrations of methylated Hg species in the marine boundary layer varied significantly among our sites, with a predominance of MMHg over Hudson Bay (HB), and DMHg over Canadian Arctic Archipelago (CAA) waters. We concluded that DMHg is of marine origin and that primary production rate and sea-ice cover are major drivers of its concentration in the Canadian Arctic marine boundary layer. Summer wet deposition rates of atmospheric MMHg, likely to be the product of DMHg degradation in the atmosphere, were estimated at 188 ± 117.5 ng m(-2) and 37 ± 21.7 ng m(-2) for HB and CAA, respectively, sustaining MMHg concentrations available for biomagnification in the pelagic food web.