Ken O. Buesseler

A mesoscale phytoplankton bloom in the polar Southern Ocean stimulated by iron fertilization

Changes in iron supply to oceanic plankton are thought to have a significant effect on concentrations of atmospheric carbon dioxide by altering rates of carbon sequestration, a theory known as the ‘iron hypothesis’. For this reason, it is important to understand the response of pelagic biota to increased iron supply. Here we report the results of a mesoscale iron fertilization experiment in the polar Southern Ocean, where the potential to sequester iron-elevated algal carbon is probably greatest. Increased iron supply led to elevated phytoplankton biomass and rates of photosynthesis in surface waters, causing a large drawdown of carbon dioxide and macronutrients, and elevated dimethyl sulphide levels after 13 days. This drawdown was mostly due to the proliferation of diatom stocks. But downward export of biogenic carbon was not increased. Moreover, satellite observations of this massive bloom 30 days later, suggest that a sufficient proportion of the added iron was retained in surface waters. Our findings demonstrate that iron supply controls phytoplankton growth and community composition during summer in these polar Southern Ocean waters, but the fate of algal carbon remains unknown and depends on the interplay between the processes controlling export, remineralisation and timescales of water mass subduction.

Synthesis of iron fertilization experiments: From the Iron Age in the Age of Enlightenment

Comparison of eight iron experiments shows that maximum Chl a, the maximum DIC removal, and the overall DIC/Fe efficiency all scale inversely with depth of the wind mixed layer (WML) defining the light environment. Moreover, lateral patch dilution, sea surface irradiance, temperature, and grazing play additional roles. The Southern Ocean experiments were most influenced by very deep WMLs. In contrast, light conditions were most favorable during SEEDS and SERIES as well as during IronEx-2. The two extreme experiments, EisenEx and SEEDS, can be linked via EisenEx bottle incubations with shallower simulated WML depth. Large diatoms always benefit the most from Fe addition, where a remarkably small group of thriving diatom species is dominated by universal response of Pseudo-nitzschia spp. Significant response of these moderate (10–30 μm), medium (30–60 μm), and large (>60 μm) diatoms is consistent with growth physiology determined for single species in natural seawater. The minimum level of “dissolved” Fe (filtrate < 0.2 μm) maintained during an experiment determines the dominant diatom size class. However, this is further complicated by continuous transfer of original truly dissolved reduced Fe(II) into the colloidal pool, which may constitute some 75% of the “dissolved” pool. Depth integration of carbon inventory changes partly compensates the adverse effects of a deep WML due to its greater integration depths, decreasing the differences in responses between the eight experiments. About half of depth-integrated overall primary productivity is reflected in a decrease of DIC. The overall C/Fe efficiency of DIC uptake is DIC/Fe ∼ 5600 for all eight experiments. The increase of particulate organic carbon is about a quarter of the primary production, suggesting food web losses for the other three quarters. Replenishment of DIC by air/sea exchange tends to be a minor few percent of primary CO2 fixation but will continue well after observations have stopped. Export of carbon into deeper waters is difficult to assess and is until now firmly proven and quite modest in only two experiments.

The decoupling of production and particulate export in the surface ocean

The relationship between primary production in the surface ocean and export of particulate organic carbon (POC) on sinking particles is examined in studies that have utilized 234Th as a tracer of upper ocean export. Comparisons between production and export are made in a wide range of open ocean settings and seasons. The results indicate that much of the ocean is characterized by low POC export relative to primary production (export/production = ThE < 5–10%). Exceptions to this pattern are found during blooms at high latitudes, accompanying spring blooms at midlatitudes, and perhaps in association with more episodic export pulses. These sites of high export are most often characterized by food webs dominated by large phytoplankton, in particular diatoms. These results can be used to better parameterize surface export in biogeochemical models in order to provide a more accurate prediction of the flow of C and associated nutrients in the oceans.

Eddy/Wind Interactions Stimulate Extraordinary Mid-Ocean Plankton Blooms

Episodic eddy-driven upwelling may supply a significant fraction of the nutrients required to sustain primary productivity of the subtropical ocean. New observations in the northwest Atlantic reveal that, although plankton blooms occur in both cyclones and mode-water eddies, the biological responses differ. Mode-water eddies can generate extraordinary diatom biomass and primary production at depth, relative to the time series near Bermuda. These blooms are sustained by eddy/wind interactions, which amplify the eddy-induced upwelling. In contrast, eddy/wind interactions dampen eddy-induced upwelling in cyclones. Carbon export inferred from oxygen anomalies in eddy cores is one to three times as much as annual new production for the region.

Carbon and nitrogen export during the JGOFS North Atlantic Bloom experiment estimated from 234Th: 238U disequilibria

Abstract The disequilibrium between the particle-reactive tracer 234 Th ( t 1 2 = 24.1 days) and its soluble parent, 238 U, was used to examine Th scavenging and export fluxes during the U.S. JGOFS North Atlantic Bloom Experiment (24 April–30 May 1989) at ∼47°N, 20°W. Four profiles of dissolved and particulate 234 Th in the upper 300 m and a non-steady box model were used to quantify dissolved 234 Th uptake and particle export rates. The highest export fluxes occured during the first half of May. From POC/ 234 Th and PON/ 234 Th ratios, particulate organic C and N fluxes were calculated. Results were 5–41 mmol C m −2 day −1 and 0.9–6.5 mmol N m −2 day −1 from the 0–35 m layer. The ratio of POC export flux to primary production ranged from 0.05 to 0.42, peaking in the first half of May. The estimated fluxes agree with the observed losses of total C and N from the upper ocean during the bloom, but yield significantly higher fluxes than were measured by floating traps at 150 and 300 m.

An assessment of the use of sediment traps for estimating upper ocean particle fluxes

This review provides an assessment of sediment trap accuracy issues by gathering data to address trap hydrodynamics, the problem of zooplankton “swimmers,” and the solubilization of material after collection. For each topic, the problem is identified, its magnitude and causes reviewed using selected examples, and an update on methods to correct for the potential bias or minimize the problem using new technologies is presented. To minimize hydrodynamic biases due to flow over the trap mouth, the use of neutrally buoyant sediment traps is encouraged. The influence of swimmers is best minimized using traps that limit zooplankton access to the sample collection chamber. New data on the impact of different swimmer removal protocols at the US time-series sites HOT and BATS are compared and shown to be important. Recent data on solubilization are compiled and assessed suggesting selective losses from sinking particles to the trap supernatant after collection, which may alter both fluxes and ratios of elements in long term and typically deeper trap deployments. Different methods are needed to assess shallow and short- term trap solubilization effects, but thus far new incubation experiments suggest these impacts to be small for most elements. A discussion of trap calibration methods reviews independent assessments of flux, including elemental budgets, particle abundance and flux modeling, and emphasizes the utility of U-Th radionuclide calibration methods.

Impacts of the Fukushima Nuclear Power Plants on Marine Radioactivity

The impacts on the ocean of releases of radionuclides from the Fukushima Dai-ichi nuclear power plants remain unclear. However, information has been made public regarding the concentrations of radioactive isotopes of iodine and cesium in ocean water near the discharge point. These data allow us to draw some basic conclusions about the relative levels of radionuclides released which can be compared to prior ocean studies and be used to address dose consequences as discussed by Garnier-Laplace et al. in this journal. The data show peak ocean discharges in early April, one month after the earthquake and a factor of 1000 decrease in the month following. Interestingly, the concentrations through the end of July remain higher than expected implying continued releases from the reactors or other contaminated sources, such as groundwater or coastal sediments. By July, levels of (137)Cs are still more than 10,000 times higher than levels measured in 2010 in the coastal waters off Japan. Although some radionuclides are significantly elevated, dose calculations suggest minimal impact on marine biota or humans due to direct exposure in surrounding ocean waters, though considerations for biological uptake and consumption of seafood are discussed and further study is warranted.

Fukushima-derived radionuclides in the ocean and biota off Japan

The Tōhoku earthquake and tsunami of March 11, 2011, resulted in unprecedented radioactivity releases from the Fukushima Dai-ichi nuclear power plants to the Northwest Pacific Ocean. Results are presented here from an international study of radionuclide contaminants in surface and subsurface waters, as well as in zooplankton and fish, off Japan in June 2011. A major finding is detection of Fukushima-derived 134Cs and 137Cs throughout waters 30–600 km offshore, with the highest activities associated with near-shore eddies and the Kuroshio Current acting as a southern boundary for transport. Fukushima-derived Cs isotopes were also detected in zooplankton and mesopelagic fish, and unique to this study we also find 110mAg in zooplankton. Vertical profiles are used to calculate a total inventory of ∼2 PBq 137Cs in an ocean area of 150,000 km2. Our results can only be understood in the context of our drifter data and an oceanographic model that shows rapid advection of contaminants further out in the Pacific. Importantly, our data are consistent with higher estimates of the magnitude of Fukushima fallout and direct releases [Stohl et al. (2011) Atmos Chem Phys Discuss 11:28319–28394; Bailly du Bois et al. (2011) J Environ Radioact, 10.1016/j.jenvrad.2011.11.015]. We address risks to public health and marine biota by showing that though Cs isotopes are elevated 10–1,000× over prior levels in waters off Japan, radiation risks due to these radionuclides are below those generally considered harmful to marine animals and human consumers, and even below those from naturally occurring radionuclides.

Regional estimates of the export flux of particulate organic carbon derived from thorium-234 during the JGOFS EQPAC program

Abstract The upper ocean 234Th activity distribution at 77 stations was measured between 12°N and 10°S, and 95°W and 170°W in the spring and autumn of 1992. A regional scavenging model was used to estimate vertical export of particulate 234Th. Given the relatively high upwelling rates in this region, particularly at equatorial latitudes near 140°W, it was necessary to include upwelling of 234Th in our model in order to quantify particulate export. Using this export flux and the measured organic C or N to 234Th ratio on particles, one can empirically determine POC and PON fluxes for this region. The estimated particulate organic C flux varies spatially and temporally within this region, ranging from 1 to 7 mmol C m−2 day−1, with enhanced export occurring over the equator. Fluxes are also enhanced along 95°W coincident with a low temperature/high nutrient peak at 4°S. Along 140°W, particulate organic C export from the upper 100 m is on the order of 2 mmol C m−2 day−1 at latitudes beyond 4°N and 4°S, with an equatorial peak of 3–5 mmol C m−2 day−1 in both spring and fall. These results suggest that a relatively small per cent of the total production is exported locally on sinking particles (particle export/primary production C 234 Th ratios. Given the measured C N ratio, particulate N fluxes from the upper 100 m would be 6 times lower than for POC.

A time-series study of particulate matter export in the North Pacific Subtropical Gyre based on 234Th : 238U disequilibrium

Depth profiles oftotal 234 Th (dissolved+particulate) were collected at Station ALOHA (22145N, 158100W) in the North Pacific Subtropical Gyre during 9 cruises from April 1999 to March 2000. Samples were collected and processed by a new 2 L technique that enables more detailed depth resolution then previous 234 Th studies. Significant zones ofparticle export ( 234 Th deficiency) and particle remineralization ( 234 Th excess) were measured both temporally and with depth. 234 Th derived particulate carbon (PC) and nitrogen (PN) fluxes were determined with steady-state and non-steady-state models and PC/ 234 Th and PN/ 234 Th ratios measured with both in situ pumps and free-drifting particle interceptor traps deployed at 150 m. 234 Th based export estimates of4.0 72.3 mmol C m � 2 d � 1 and 0.5370.19 mmol N m � 2 d � 1 , were approximately 60% higher than those measured in PIT style sediment traps from the same time period, 2.470.2 mmol C m � 2 d � 1 and 0.3270.08 mmol N m � 2 d � 1 . Most ofthis difference is attributable to two large export events that occurred during October and December 1999, when traps undercollected for 234 Th by a factor of 2 to 4. 234 Th export (ThE) ratios based on 234 Th derived PC flux/ 14 C based primary production ranged from 4% to 22% (average=8.8%). Our results confirm the recent estimates of C export by Emerson et al. (Nature 389 (1997) 951) and Sonnerup et al. (Deep-Sea Research I 46 (1999) 777) and indicate that C export from the oligotrophic ocean must be considered when discussing C sequestration in global climate change. r 2001 Elsevier Science Ltd. All rights reserved.