Manganese (Mn) is an essential element for photosynthetic life, yet concentrations in Southern Ocean open waters are very low, resulting from biological uptake along with limited external inputs. At southern latitudes, waters overlying the Antarctic shelf are expected to have much higher Mn concentrations due to their proximity to external sources such as sediment and sea ice. In this study, we investigated the potential export of Mn-rich Antarctic shelf waters toward depleted open Southern Ocean waters. Our results showed that while high Mn concentrations were observed over the shelf, strong biological uptake decreased dissolved Mn concentrations in surface waters north of the Southern Antarctic Circumpolar Current Front (< 0.1 nM), limiting export of shelf Mn to the open Southern Ocean. Conversely, in bottom waters, mixing between Mn-rich Antarctic Bottom Waters and Mn-depleted Low Circumpolar Deep Waters combined with scavenging processes led to a decrease in dissolved Mn concentrations with distance from the coast. Subsurface dissolved Mn maxima represented a potential reservoir for surface waters (0.3 – 0.6 nM). However, these high subsurface values decreased with distance from the coast, suggesting these features may result from external sources near the shelf in addition to particle remineralization. Overall, these results imply that the lower-than-expected lateral export of trace metal-enriched waters contributes to the extremely low (< 0.1 nM) and potentially co-limiting Mn concentrations previously reported further north in this Southern Ocean region.
The Southern Ocean is the largest region in which iron limits the growth of phytoplankton. However, a phytoplankton bloom thousands of square kilometres in area forms each spring-summer in the Indian sector of the Southern Ocean, both above and to the east of the Kerguelen Plateau. The central region of the Kerguelen Plateau hosts the volcanically active islands, Heard and McDonald (HIMI), the former of which is largely covered by glaciers. The sources and processes governing supply of iron from HIMI to the region are relatively unknown. In the austral summer of 2016, the first voyage to focus on biogeochemical cycling in the HIMI region was undertaken (GEOTRACES process study GIpr05). Using iron redox measurements, we show here that each of the adjacent islands are strong sources of dissolved iron(II) (DFe(II)), though controlled by different supply mechanisms. At Heard Island, the greatest DFe(II) concentrations (max 0.57 nmol L) were detected north of the island. An inverse correlation of DFe(II) concentrations with salinity suggests the origin is from a sea-terminating glacier on the island. At McDonald Islands, the greatest DFe(II) concentrations (max 1.01 nmol L) were detected east of the islands which, based on DFe(II) profiles from five targeted stations, appears likely to originate from shallow diffuse hydrothermalism. Elevated DFe(II) around HIMI may increase Fe availability for biota and indicate slower oxidation kinetics in the region, which has implications for transport of Fe away from the islands to the broader northern Kerguelen Plateau where the annual plankton bloom is strongest.

Toshimasa Doi

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The availability of dissolved iron (dFe) exerts an important control on primary production. Recent ocean observation programs have provided information on dFe in many parts of the ocean, but knowledge is still limited concerning the rates of processes that control the concentrations and cycling of dFe in the ocean and hence the role of dFe as a determinant of global primary production. We constructed a three-dimensional gridded dataset of oceanic dFe concentrations by using both observations and a simple model of the iron cycle, and estimated the difference of processes among the ocean basins in controlling the dFe distributions. A Green’s function approach was used to integrate the observations and the model. The reproduced three-dimensional dFe distribution indicated that iron influx from aeolian dust and from shelf sediment were 7.6 Gmol yr and 4.4 Gmol yr in the Atlantic Ocean and 0.4 Gmol yr and 4.1 Gmol yr in the Pacific Ocean. The residence times were estimated to be 12.2 years in the Atlantic and 80.4 years in the Pacific. These estimates imply large differences in the cycling of dFe between the two ocean basins that would need to be taken into consideration when projecting future iron biogeochemical cycling under different climate change scenarios. Although there is some uncertainty in our estimates, global estimates of iron cycle characteristics based on this approach can be expected to enhance our understanding of the material cycle and hence of the current and future rates of marine primary production.