Paul J. Morris

Southern Ocean deep-water carbon export enhanced by natural iron fertilization

The addition of iron to high-nutrient, low-chlorophyll regions induces phytoplankton blooms that take up carbon. Carbon export from the surface layer and, in particular, the ability of the ocean and sediments to sequester carbon for many years remains, however, poorly quantified. Here we report data from the CROZEX experiment in the Southern Ocean, which was conducted to test the hypothesis that the observed north–south gradient in phytoplankton concentrations in the vicinity of the Crozet Islands is induced by natural iron fertilization that results in enhanced organic carbon flux to the deep ocean. We report annual particulate carbon fluxes out of the surface layer, at three kilometres below the ocean surface and to the ocean floor. We find that carbon fluxes from a highly productive, naturally iron-fertilized region of the sub-Antarctic Southern Ocean are two to three times larger than the carbon fluxes from an adjacent high-nutrient, low-chlorophyll area not fertilized by iron. Our findings support the hypothesis that increased iron supply to the glacial sub-Antarctic may have directly enhanced carbon export to the deep ocean. The CROZEX sequestration efficiency (the amount of carbon sequestered below the depth of winter mixing for a given iron supply) of 8,600 mol mol-1 was 18 times greater than that of a phytoplankton bloom induced artificially by adding iron, but 77 times smaller than that of another bloom initiated, like CROZEX, by a natural supply of iron. Large losses of purposefully added iron can explain the lower efficiency of the induced bloom6. The discrepancy between the blooms naturally supplied with iron may result in part from an underestimate of horizontal iron supply.

Global carbon cycle (communication arising): Metabolic balance of the open sea

The rise of oxygenic photosynthesis nearly three billion years ago led to the accumulation of free oxygen and to the subsequent diversification of life on Earth; today, nearly half of all oxygen production derives from the photosynthetic activities of marine phytoplankton. The conclusion that the open sea –– and therefore much of our planets surface –– is in a net heterotrophic metabolic state is enigmatic and is a first-order question in the global carbon cycle, as discussed by del Giorgio and Duarte. Our findings suggest that autotrophy in the open sea is episodic and decoupled from the more constant heterotrophic processes. Consequently, the metabolic balance of the open sea depends on proper space and timescale integration to achieve an ecological understanding of life in the sea.

Fukushima Daiichi–Derived Radionuclides in the Ocean: Transport, Fate, and Impacts

The events that followed the Tohoku earthquake and tsunami on March 11, 2011, included the loss of power and overheating at the Fukushima Daiichi nuclear power plants, which led to extensive releases of radioactive gases, volatiles, and liquids, particularly to the coastal ocean. The fate of these radionuclides depends in large part on their oceanic geochemistry, physical processes, and biological uptake. Whereas radioactivity on land can be resampled and its distribution mapped, releases to the marine environment are harder to characterize owing to variability in ocean currents and the general challenges of sampling at sea. Five years later, it is appropriate to review what happened in terms of the sources, transport, and fate of these radionuclides in the ocean. In addition to the oceanic behavior of these contaminants, this review considers the potential health effects and societal impacts.

On the proportion of ballast versus non-ballast associated carbon export in the surface ocean

The role of biominerals in driving carbon export from the surface ocean is unclear. We compiled surface particulate organic carbon (POC), and mineral ballast export fluxes from 55 different locations in the Atlantic and Southern Oceans. Substantial surface POC export accompanied by negligible mineral export was recorded implying that association with mineral phases is not a precondition for organic export to occur. The proportion of non-mineral associated sinking POC ranged from 0 to 80% and was highest in areas previously shown to be dominated by diatoms. This is consistent with previous estimates showing that transfer efficiency in such regions is low. However we propose that, rather than the low transfer efficiency arising from diatom blooms being inherently characterized by poorly packaged aggregates which are efficiently exported but which disintegrate readily in mid water, it is due to such environments having very high levels of unballasted organic C export.

Fluxes of particulate iron from the upper ocean around the Crozet Islands: A naturally iron-fertilized environment in the Southern Ocean

Despite a large macronutrient reservoir, the Southern Ocean has low levels of chlorophyll, primarily due to low iron availability. Exceptions to this situation are island systems where natural terrestrial iron inputs allow the development of large blooms. Particulate organic carbon (POC) and particulate (labile and refractory) iron analyses were performed on large (>53 μm) particles collected at the base of the mixed layer within such a system (the Crozet Islands) and in adjacent high-nutrient, low-chlorophyll (HNLC) waters. Biogenic iron was obtained by removal of estimated lithogenic Fe from the total Fe present. We combine these data with 234Th measurements to determine downward particulate Fe fluxes. Fluxes of Fe ranged from 4 to 301 nmol m−2 d−1 (labile), not detectable to 50 μmol m−2 d−1 (biogenic), and from 3 to 145 μmol m−2 d−1 (total) and, on average, were approximately four times larger below the highly productive, naturally iron-fertilized region than below the adjacent HNLC area. Downward labile iron fluxes are close to the sum of dissolved terrestrial, atmospheric, and upwelled iron calculated from the Planquette et al. (2007), model. Refractory iron fluxes are ∼2 orders of magnitude larger, and these can only have come from particles advected from the plateau itself. The “biogenic Fe,” is a substantial fraction (0–76, mean 23%) of the total particulate Fe to the north of the islands. The origin of this Fe pool must be dominantly biological conversion from the lithogenic fraction, as other supply terms including aeolian, deep mixing, and lateral advection of dissolved Fe are inadequate to account for the magnitude of this Fe. Inclusion of the offshore biologically available fraction of the lithogenic iron flux is therefore required to calculate fully the yield of carbon exported per unit iron injected.

A carbon budget for a naturally iron fertilized bloom in the Southern Ocean

Subantarctic islands in the high-nutrient, low-chlorophyll (HNLC) Southern Ocean are natural sources of iron and stimulate blooms in their proximity, such as the one observed close to the Crozet Islands (52°E, 46°S). During 2004/2005, particulate organic carbon (POC) export was measured using the 234Th technique in the Crozet bloom and compared with an HNLC control region. Initial results showed that iron release had no effect on daily POC export rates, thus any iron-driven enhancement in POC export was due to a longer export phase in the bloom region when compared to the control region. The duration of the export event was empirically estimated by closing the silicon budget, thus allowing seasonal POC export to be calculated by applying the export duration to the daily rates of POC export. This yields a seasonal estimate of POC export that is 3.6 times larger (range 1.9–7.1) in the iron-fertilized region than in the HNLC control region. These estimates of POC export were then compared to independent estimates of organic matter storage in the upper ocean, which are significant in both the HNLC and control regions. Overall, integrated POC export was significantly (approximately 50%) lower than estimated seasonal new production, the fraction of production that is supported by inputs of new nutrients. Finally, the sequestration efficiency, the numerical relationship between the supply of the limiting nutrient, iron, and the key ecosystem function of POC export at 100 m, is estimated to be 16,790 mol:mol.