Iron is an essential nutrient that regulates productivity in ~30% of the ocean. Compared with deep (>2000 meter) hydrothermal activity at mid-ocean ridges that provide iron to the ocean’s interior, shallow (<500 meter) hydrothermal fluids are likely to influence the surface’s ecosystem. However, their effect is unknown. In this work, we show that fluids emitted along the Tonga volcanic arc (South Pacific) have a substantial impact on iron concentrations in the photic layer through vertical diffusion. This enrichment stimulates biological activity, resulting in an extensive patch of chlorophyll (360,000 square kilometers). Diazotroph activity is two to eight times higher and carbon export fluxes are two to three times higher in iron-enriched waters than in adjacent unfertilized waters. Such findings reveal a previously undescribed mechanism of natural iron fertilization in the ocean that fuels regional hotspot sinks for atmospheric CO ₂ .

Key Points: Size‐fractionation reveals that colloidal iron is more important than soluble iron for distribution of dissolved iron in North Atlantic Colloidal iron is the predominantly active species at key supply and removal processes of the dissolved iron cycle Global comparison suggests that the colloidal iron fraction in mesopelagic zone is determined by the local lithogenic contribution

In the Western Tropical South Pacific, a hotspot of dinitrogen‐fixing organisms has been identified. The survival of these species depends on the availability of dissolved iron (DFe); however, the source of this DFe is still unclear. DFe was measured along a transect from 175°E to 166°W near 19–21°S. The distribution of DFe showed high spatial variability: low concentrations (∼0.2 nmol kg⁻¹) in the South Pacific gyre and high concentrations (up to 50 nmol kg⁻¹) in the west of the Tonga arc, indicating that this arc is a clear boundary between iron‐poor and iron‐rich waters. An optimal multiparameter analysis was used to distinguish the relative importance of physical transport relative to non‐conservative processes on the observed distribution. This analysis demonstrated that the shallow hydrothermal sources present along the Tonga‐Kermadec arc are responsible for the high concentrations observed in the photic layer. Nevertheless, in contrast to what has been observed for deep hydrothermal plumes, our results highlighted the rapid decrease in DFe concentrations near shallow hydrothermal sources. This is likely due to a shorter residence time of surface water masses combined with several biogeochemical processes at play (precipitation, scavenging, biological uptake, and photoreduction). This study clearly highlights the role of shallow hydrothermal sources on the DFe cycle within the Tonga‐Kermadec arc where a strong link to biological activity in surface waters can be assessed, despite the small but significant fraction of DFe ultimately stabilized. It also emphasizes the need to consider the impact of these sources for a better understanding of the global iron cycle.

Methylmercury is a potent toxin threatening the global population mainly through the consumption of marine fish. Hydrothermal venting directly delivers natural mercury to the ocean, yet its global flux remains poorly constrained. To determine the extent to which anthropogenic inputs have increased oceanic mercury levels, it is crucial to estimate natural mercury levels. Here we combine observations of vent fluids, plume waters, seawater and rock samples to quantify the release of mercury from the Trans-Atlantic Geotraverse hydrothermal vent at the Mid-Atlantic Ridge. The majority (67–95%) of the mercury enriched in the vent fluids (4,966 ± 497 pmol l⁻¹) is rapidly diluted to reach background seawater levels (0.80 pmol l⁻¹). A small Hg fraction (2.6–10%) is scavenged to the Trans-Atlantic Geotraverse mound rocks. Scaling up our findings and previous work, we propose a mercury flux estimate of 1.5–64.7 t per year from mid-ocean ridges. This hydrothermal flux is small in comparison to anthropogenic inputs. This suggests that most of the mercury present in the ocean must be of anthropogenic origin and that the implementation of emissions reduction measures outlined in the Minamata Convention could effectively reduce mercury levels in the global ocean and subsequently in marine fish.

The availability of iron (Fe) can seasonally limit phytoplankton growth in the High Latitude North Atlantic (HLNA), greatly reducing the efficiency of the biological carbon pump. However, the spatial extent of seasonal iron limitation is not yet known. We present autumn nutrient and dissolved Fe measurements, combined with microphytoplankton distribution, of waters overlying the Hebridean (Scottish) shelf break. A distinct biogeochemical divide was observed, with Fe deficient surface waters present beyond the shelf break, much further eastwards than previously recognised. Due to along and on-shelf circulation, the Hebridean shelf represents a much-localised source of Fe, which does not fertilise the wider HLNA. Shelf sediments are generally thought to supply large quantities of Fe to overlying waters. However, for this Fe to influence upper-ocean biogeochemical cycling, efficient off-shelf transport mechanisms are required. This work challenges the view that the oceanic surface waters in close proximity to continental margins are iron replete with respect to marine primary production demands.