Explore the vast range of titles available.

Presents essays responding to a question about what scientific term or concept ought to be more widely known, written by such authors as Jared Diamond, Richard Thaler, Richard Dawkins, Lisa Randall, Steven Pinker, and Carlo Roveri.

Zinc, a key micronutrient for marine phytoplankton, has a global distribution remarkably similar to that of silicic acid, even though Zn and Si have very different biogeochemical cycles. Weber et al. investigated why this is so by combining model calculations and observations. They found that biological uptake in the Southern Ocean and reversible scavenging of Zn onto sinking particles both affect the distribution of Zn in the ocean. Thus, Zn and Si distributions will be affected differently by future changes in ocean temperature, pH, and carbon fluxes. Science , this issue p. 72 The distribution of zinc in the world oceans depends on circulation, organic matter cycling, and reversible scavenging. Zinc (Zn) is a key micronutrient for marine phytoplankton, with a global distribution that is similar to silicic acid. The processes that govern this relationship, despite the very different biological cycling of Zn and silica, remain poorly understood. Here, we use diagnostic and mechanistic models to show that only a combination of Southern Ocean biological uptake and reversible scavenging of Zn onto sinking particles can explain the observations. The distinction between organic and adsorbed Zn can also reconcile the vertical distribution and mass balance of Zn isotopes, which previously appeared at odds. This holistic understanding explains the Zn deficiencies observed throughout the low-latitude ocean and implies a greater sensitivity of the marine Zn cycle to climate-driven changes in organic matter cycling than previously recognized.

Atmospheric dust is an important source of the micronutrient Fe to the oceans. Although relatively insoluble mineral Fe is assumed to be the most important component of dust, a relatively small yet highly soluble anthropogenic component may also be significant. However, quantifying the importance of anthropogenic Fe to the global oceans requires a tracer which can be used to identify and constrain anthropogenic aerosols in situ. Here, we present Fe isotope (δ 56 Fe) data from North Atlantic aerosol samples from the GEOTRACES GA03 section. While soluble aerosol samples collected near the Sahara have near-crustal δ 56 Fe, soluble aerosols from near North America and Europe instead have remarkably fractionated δ 56 Fe values (as light as −1.6‰). Here, we use these observations to fingerprint anthropogenic combustion sources, and to refine aerosol deposition modeling. We show that soluble anthropogenic aerosol Fe flux to the global surface oceans is highly likely to be underestimated, even in the dusty North Atlantic. The relative importance of crustal vs. anthropogenic dust deposition for iron cycling in the surface ocean is unclear. Based on analysis of iron isotope data from North Atlantic aerosol samples, the authors can reveal the relative importance of anthropogenic iron emissions and its impact on marine biogeochemistry.

A high-resolution oceanic section of dissolved iron stable isotope ratios reveals that the primary source of dissolved iron to the North Atlantic is atmospheric dust, while seafloor sediments and submarine volcanic vents also contribute significantly. Iron sources in the North Atlantic Ocean Iron availability limits phytoplankton growth throughout the oceans, acting as a key influence on the global carbon cycle and the oceanic response to changing climate. But large uncertainties remain as to the relative importance of the various sources of iron, including windblown dust and hydrothermal vents. This paper presents a high-resolution transect of seawater dissolved stable iron isotope ratios and iron concentrations in the North Atlantic Ocean. Saharan dust aerosol emerges as the dominant source of dissolved iron along the section, with sediments and hydrothermal vents also significant. Changes in these sources through time may have wide-ranging implications for the global carbon cycle. Dissolved iron is an essential micronutrient for marine phytoplankton, and its availability controls patterns of primary productivity and carbon cycling throughout the oceans 1 , 2 . The relative importance of different sources of iron to the oceans is not well known, however, and flux estimates from atmospheric dust, hydrothermal vents and oceanic sediments vary by orders of magnitude. Here we present a high-resolution transect of dissolved stable iron isotope ratios (δ 56 Fe) and iron concentrations ([Fe]) along a section of the North Atlantic Ocean. The different iron sources can be identified by their unique δ 56 Fe signatures, which persist throughout the water column. This allows us to calculate the relative contribution from dust, hydrothermal venting and reductive and non-reductive sedimentary release to the dissolved phase. We find that Saharan dust aerosol is the dominant source of dissolved iron along the section, contributing 71–87 per cent of dissolved iron. Additional sources of iron are non-reductive release from oxygenated sediments on the North American margin (10–19 per cent), reductive sedimentary dissolution on the African margin (1–4 per cent) and hydrothermal venting at the Mid-Atlantic Ridge (2–6 per cent). Our data also indicate that hydrothermal vents in the North Atlantic are a source of isotopically light iron, which travels thousands of kilometres from vent sites, potentially influencing surface productivity. Changes in the relative importance of the different iron sources through time may affect interactions between the carbon cycle and climate.

Dissolution of marine sediment is a key source of dissolved iron (Fe) that regulates the ocean carbon cycle. Currently, our prevailing understanding, encapsulated in ocean models, focuses on low-oxygen reductive supply mechanisms and neglects the emerging evidence from iron isotopes in seawater and sediment porewaters for additional nonreductive dissolution processes. Here, we combine measurements of Fe colloids and dissolved δ56Fe in shallow porewaters spanning the full depth of the South Atlantic Ocean to demonstrate that it is lithogenic colloid production that fuels sedimentary iron supply away from low-oxygen systems. Iron colloids are ubiquitous in these oxic ocean sediment porewaters and account for the lithogenic isotope signature of dissolved Fe (δ56Fe = +0.07 ± 0.07‰) within and between ocean basins. Isotope model experiments demonstrate that only lithogenic weathering in both oxic and nitrogenous zones, rather than precipitation or ligand complexation of reduced Fe species, can account for the production of these porewater Fe colloids. The broader covariance between colloidal Fe and organic carbon (OC) abundance suggests that sorption of OC may control the nanoscale stability of Fe minerals by inhibiting the loss of Fe(oxyhydr)oxides to more crystalline minerals in the sediment. Oxic ocean sediments can therefore generate a large exchangeable reservoir of organo-mineral Fe colloids at the sediment water interface (a “rusty source”) that dominates the benthic supply of dissolved Fe to the ocean interior, alongside reductive supply pathways from shallower continental margins.

Hydrothermally sourced dissolved metals have been recorded in all ocean basins. In the oceans’ largest known hydrothermal plume, extending westwards across the Pacific from the Southern East Pacific Rise, dissolved iron and manganese were shown by the GEOTRACES program to be transported halfway across the Pacific. Here, we report that particulate iron and manganese in the same plume also exceed background concentrations, even 4,000 km from the vent source. Both dissolved and particulate iron deepen by more than 350 m relative to 3 He—a non-reactive tracer of hydrothermal input—crossing isopycnals. Manganese shows no similar descent. Individual plume particle analyses indicate that particulate iron occurs within low-density organic matrices, consistent with its slow sinking rate of 5–10 m yr −1 . Chemical speciation and isotopic composition analyses reveal that particulate iron consists of Fe( III ) oxyhydroxides, whereas dissolved iron consists of nanoparticulate Fe( III ) oxyhydroxides and an organically complexed iron phase. The descent of plume-dissolved iron is best explained by reversible exchange onto slowly sinking particles, probably mediated by organic compounds binding iron. We suggest that in ocean regimes with high particulate iron loadings, dissolved iron fluxes may depend on the balance between stabilization in the dissolved phase and the reversibility of exchange onto sinking particles. The largest known hydrothermal plume moves dissolved iron halfway across the Pacific. In situ measurements show that dissolved and particulate iron transport is facilitated by reversible exchange of dissolved iron onto organic compounds.

Throughout the open ocean, a minimum in dissolved iron concentration (dFe) overlaps with the deep chlorophyll maximum (DCM), which marks the lower limit of the euphotic zone. Maximizing light capture in these dim waters is expected to require upregulation of Fe-bearing photosystems, further depleting dFe and possibly leading to co-limitation by both iron and light. However, this effect has not been quantified for important phytoplankton groups like Prochlorococcus , which contributes most of the productivity in the oligotrophic DCM. Here, we present culture experiments with Prochlorococcus strain MIT1214, a member of the Low Light 1 ecotype isolated from the DCM in the North Pacific subtropical gyre. Under a matrix of iron and irradiance matching those found at the DCM, the ratio of Fe to carbon in Prochlorococcus MIT1214 cells ranged from 10–40 × 10 −6  mol Fe:mol C and increased with light intensity and growth rate. These results challenge theoretical models predicting highest Fe:C at lowest light intensity, and are best explained by a large photosynthetic Fe demand that is not downregulated at higher light. To sustain primary production in the DCM with the rigid Fe requirements of low-light-adapted Prochlorococcus , dFe must be recycled rapidly and at high efficiency.

Neodymium (Nd) isotopes ratios are regarded as a key proxy for past ocean circulation despite unsettled debate on marine Nd cycle controls, which opposes a “top‐down” hypothesis (surface sources dominate) and a “bottom‐up” hypothesis (sedimentary sources dominate), each with important implications for Nd isotope proxy interpretation. We suggest a new, basin‐specific framework for interpreting Nd isotope records. Specifically, while Nd isotope records are reliable water‐mass‐mixing proxies in the Atlantic, they are likely better used as proxies of residence time in the Pacific. Here, we test these hypotheses using a computationally efficient, data‐constrained model of the marine Nd cycle. Our results show Atlantic Nd isotopes are dominated by surface sources, while Pacific Nd isotope ratios are strongly influenced by sedimentary sources. We find that shallow, reactive sediments—especially those with extremely radiogenic or unradiogenic isotopic compositions—are crucial to reproduce observed εNd profiles in the Pacific.

Fossil-fuel emissions may impact phytoplankton primary productivity and carbon cycling by supplying bioavailable Fe to remote areas of the ocean via atmospheric aerosols. However, this path-way has not been confirmed by field observations of anthropogenic Fe in seawater. Here we present high-resolution trace-metal concentrations across the North Pacific Ocean (158°W from 25°to 42°N). A dissolved Fe maximum was observed around 35°N, coincident with high dissolved Pb and Pb isotope ratios matching Asian industrial sources and confirming recent aerosol deposition. Ironstable isotopes reveal in situ evidence of anthropogenic Fe in seawater, with low δ56Fe (−0.23‰ > δ56Fe > −0.65‰) observed in the region that is most influenced by aerosol deposition. An isotope mass balance suggests that anthropogenic Fe contributes 21–59% of dissolved Fe measured between 35° and 40°N. Thus, anthropogenic aerosol Fe is likely to be an important Fe source to the North Pacific Ocean.