Russell D. Frew

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.

Role of iron, light, and silicate in controlling algal biomass in subantarctic waters SE of New Zealand

Phytoplankton processes in subantarctic (SA) waters southeast of New Zealand were studied during austral autumn and spring 1997. Chlorophyll a (0.2–0.3 μg L−1) and primary production (350–650 mg C m−2 d−1) were dominated by cells 1 nmol kg−1, there was little evidence of Fe-stressed algal populations, and Fυ/Fm approached 0.60 at the STC. In addition to these trends, waters of SA origin were occasionally observed within the STC and north of the STC, and thus survey data were interpreted with caution. In vitro Fe enrichment incubations in SA waters resulted in a switch from flavodoxin expression to that of ferredoxin, indicating the alleviation of Fe stress. In another 6-day experiment, iron-mediated increases in chlorophyll a (in particular, increases in large diatoms) were of similar magnitude to those observed in a concurrent Si/Fe enrichment; ambient silicate levels were 4 μM. A concurrent in vitro Fe enrichment, at irradiance levels comparable to the calculated mean levels experienced by cells in situ, resulted in relatively small increases (approximately twofold) in chlorophyll a. Thus, in spring, irradiance and Fe may both control diatom growth. In contrast, during summer, as mean irradiance increases and silicate levels decrease, Fe limitation, Fe/Si colimitation, or silicate limitation may determine diatom growth.

The fate of added iron during a mesoscale fertilisation experiment in the Southern Ocean

The first Southern Ocean Iron RElease Experiment (SOIREE) was performed during February 1999 in Antarctic waters south of Australia (61°S, 140°E), in order to verify whether iron supply controls the magnitude of phytoplankton production in this high nutrient low chlorophyll (HNLC) region. This paper describes iron distributions in the upper ocean during our 13-day site occupation, and presents a pelagic iron budget to account for the observed losses of dissolved and total iron from waters of the fertilised patch. Iron concentrations were measured underway during daily transects through the patch and in vertical profiles of the 65-m mixed layer. High internal consistency was noted between data obtained using contrasting sampling and analytical techniques. A pre-infusion survey confirmed the extremely low ambient dissolved (0.1 nM) and total (0.4 nM) iron concentrations. The initial enrichment elevated the dissolved iron concentration to 2.7 nM. Thereafter, dissolved iron was rapidly depleted inside the patch to 0.2-0.3 nM, necessitating three re-infusions. A distinct biological response was observed in iron-fertilised waters, relative to outside the patch, unequivocally confirming that iron limits phytoplankton growth rates and biomass at this site in summer. Our budget describing the fate of the added iron demonstrates that horizontal dispersion of fertilised waters (resulting in a quadrupling of the areal extent of the patch) and abiotic particle scavenging accounted for most of the decreases in iron concentrations inside the patch (31-58 and 12-49 of added iron, respectively). The magnitude of these loss processes altered towards the end of SOIREE, and on days 12-13 dissolved (1.1 nM) and total (2.3 nM) iron concentrations remained elevated compared to surrounding waters. At this time, the biogenic iron pool (0.1 nM) accounted for only 1-2 of the total added iron. Large pennate diatoms (> 20 μm) and autotrophic flagellates (2-20 μm) were the dominant algal groups in the patch, taking up the added iron and representing 13 and 39 of the biogenic iron pool, respectively. Iron regeneration by grazers was tightly coupled to uptake by phytoplankton and bacteria, indicating that biological Fe cycling within the bloom was self-sustaining. A concurrent increase in the concentration of iron-binding ligands on days 11-12 probably retained dissolved iron within the mixed layer. Ocean colour satellite images in late March suggest that the bloom was still actively growing 42 days after the onset of SOIREE, and hence by inference that sufficient iron was maintained in the patch for this period to meet algal requirements. This raises fundamental questions regarding the biogeochemical cycling of iron in the Southern Ocean and, in particular, how bioavailable iron was retained in surface waters and/or within the biota to sustain algal growth.

Retention of dissolved iron and Fe II in an iron induced Southern Ocean phytoplankton bloom

During the 13 day Southern Ocean Iron RE-lease Experiment (SOIREE), dissolved iron concentrations decreased rapidly following each of three iron-enrichments, but remained high (>1 nM, up to 80% as FeII) after the fourth and final enrichment on day 8. The former trend was mainly due to dilution (spreading of iron-fertilized waters) and particle scavenging. The latter may only be explained by a joint production-maintenance mechanism; photoreduction is the only candidate process able to produce sufficiently high FeII, but as such levels persisted overnight (8 hr dark period) —ten times the half—life for this species—a maintenance mechanism (complexation of FeII) is required, and is supported by evidence of increased ligand concentrations on day 12. The source of these ligands and their affinity for FeII is not known. This retention of iron probably permitted the longevity of this bloom raising fundamental questions about iron cycling in HNLC (High Nitrate Low Chlorophyll) Polar waters.

Macronutrient and trace-metal geochemistry of an in situ iron-induced Southern Ocean bloom

Abstract We have investigated the effect of iron supply and increased phytoplankton growth on the cycling of the macronutrients phosphate, nitrate and silicic acid as well as the micronutrients copper (Cu), nickel (Ni), zinc (Zn) and cadmium (Cd). Nutrient levels were measured in situ in an iron-induced phytoplankton bloom at 61°S 140°E in the Southern Ocean Iron Release experiment (SOIREE). Nutrient ratios upon arrival at the study site indicate that much of the seasonal phytoplankton productivity was by iron-limited diatoms growing at low mean light levels. The addition of iron (Fe) induced a bloom that led to a draw-down in the macronutrients in ratios consistent with the growth of diatoms under iron-replete conditions. None of the bioutilised trace metals Cu, Ni, Zn or Cd showed any indication of co-limitation, with Fe, of phytoplankton growth. Zn concentrations did not decrease by algal uptake as expected. Cd was partitioned to the particulate phase indicating consumption by the algae. Cd was preferentially utilised with respect to P with a α Cd/P =5.8. Interpretation of the Cd/Ca data from the sedimentary record using this higher induced α Cd/P value would imply even higher Southern Ocean surface water P during the last glacial maximum.

The oxygen isotope composition of water masses in the northern North Atlantic

The ratio of oxygen-18 to oxygen-16 (expressed as per mille deviations from Vienna Standard Mean Ocean Water, 18O) is reported for seawater samples collected from seven full-depth CTD casts in the northern North Atlantic between 20° and 41°W, 52° and 60°N. Water masses in the study region are distinguished by their 18O composition, as are the processes involved in their formation. The isotopically heaviest surface waters occur in the eastern region where values of 18O and salinity (S) lie on an evaporation–precipitation line with slope of 0.6 in 18O–S space. Surface isotopic values become progressively lighter to the west of the region due to the addition of 18O-depleted precipitation. This appears to be mainly the meteoric water outflow from the Arctic rather than local precipitation. Surface samples near the southwest of the survey area (close to the Charlie Gibbs Fracture Zone) show a deviation in 18O–S space from the precipitation mixing line due to the influence of sea ice meltwater. We speculate that this is the effect of the sea ice meltwater efflux from the Labrador Sea. Subpolar Mode Water (SPMW) is modified en route to the Labrador Sea where it forms Labrador Sea Water (LSW). LSW lies to the right (saline) side of the precipitation mixing line, indicating that there is a positive net sea ice formation from its source waters. We estimate that a sea ice deficit of ?250 km3 is incorporated annually into LSW. This ice forms further north from the Labrador Sea, but its effect is transferred to the Labrador Sea via, e.g. the East Greenland Current. East Greenland Current waters are relatively fresh due to dilution with a large amount of meteoric water, but also contain waters that have had a significant amount of sea ice formed from them. The Northeast Atlantic Deep Water (NEADW, 18O=0.22‰) and Northwest Atlantic Bottom Waters (NWABW, 18O=0.13‰) are isotopically distinct reflecting different formation and mixing processes. NEADW lies on the North Atlantic precipitation mixing line in 18O–salinity space, whereas NWABW lies between NEADW and LSW on 18O–salinity plots. The offset of NWABW relative to the North Atlantic precipitation mixing line is partially due to entrainment of LSW by the Denmark Strait overflow water during its overflow of the Denmark Strait sill. In the eastern basin, lower deep water (LDW, modified Antarctic bottom water) is identified as far north as 55°N. This LDW has 18O of 0.13‰, making it quite distinct from NEADW. It is also warmer than NWABW, despite having a similar isotopic composition to this latter water mass.

Platelet ice and the land-fast sea ice of McMurdo Sound, Antarctica

Abstract Dendritic crystals of platelet ice appear beneath the columnar land-fast sea ice of McMurdo Sound, Antarctica. These leaf-like crystals are frozen into place by the advancing columnar growth. The platelets most probably begin to appear during July although in some parts of the Sound they may not appear at all. In addition, the amount and extent of platelet ice within the Sound varies from year to year. Previous authors have suggested that the formation of platelet ice is linked to the presence of the nearby ice shelf. It is a matter of debate whether these platelets form at depth and then float upwards or whether they grow in slightly supercooled water at the ice/water interface. The phenomenon is similar to that observed in the Weddell Sea region, but previous authors have suggested the two regions may experience different processes. This paper presents the results of field-work conducted in McMurdo Sound in 1999. Ice-structure analysis, isotopic analysis and salinity and temperature measurements near the ice/water interface are presented. Freezing points are calculated, and the possible existence of supercooling is discussed in relation to existing conjectures about the origin of platelets.

Distribution of oxygen isotopes in the water masses of Drake Passage and the South Atlantic

Measurements of the ratio of stable isotopes of oxygen (18O and 16O) from samples collected on World Ocean Circulation Experiment sections SR1b (eastern Drake Passage) and A11 (Punta Arenas to Cape Town) are used, together with hydrographic data, to deduce information about the formation and variability of South Atlantic and Southern Ocean water masses. The Drake Passage surface waters south of the Polar Front (PF) are isotopically light (δ18O around −0.4‰) owing to the influence of meteoric waters. The salinity and δ18O of the A11 surface waters yield an apparent freshwater end-member which is much isotopically lighter than the local precipitation, thus advection of these waters from farther south dominates over local effects in determining the surface water properties. The Drake Passage section shows unusual proximity of the two main fronts of the Antarctic Circumpolar Current (the PF and Subantarctic Front (SAF)), and we observe cold, fresh, and isotopically light water derived from the temperature-minimum Winter Water at the SAF. This water is of the correct density to freshen the intermediate water north of the SAF and thus play a role in the formation of the comparatively fresh Antarctic Intermediate Water (AAIW) of the South Atlantic. This confirms the role of Antarctic water in forming the South Atlantic variety of AAIW. Across the A11 section the oxygen isotope and salinity data at the AAIW core show very similar traces, with waters in the Malvinas Current loop showing lowest values of both. At the eastern boundary of the South Atlantic, the input of Red Sea Water from east of South Africa is observed via the presence of anomalously isotopically heavy AAIW. We deduce potentially significant temporal variability in the isotopic composition of Weddell Sea Deep Water (WSDW) by comparing the Drake Passage data to earlier data covering the outflow of the Weddell Sea. The A11 data show WSDW consistent with such variability, indicating that its effects could persist in the waters as they flow north into the western South Atlantic. We speculate that such variability could be due to small changes in the amount of glacial ice melt in WSDW.

Cadmium-phosphorus cycling at the subtropical convergence south of New Zealand

The water column distributions of cadmium (Cd) and phosphorus (P) in the region of the subtropical convergence (STC) south of New Zealand have been studied. Mixed layer Cd concentrations were extremely low throughout the study area, varying from 0.012 to 0.059 nmol kg−1. In subantarctic waters south of the STC, deep-water Cd concentrations were intermediate between those of the North Atlantic and the North Pacific oceans, consistent with deep-water circulation. Cd varied linearly with P with a slope of 0.35 × 10−3 mol Cdmol P, but waters in the upper 1000 m were significantly depleted in Cd compared to temperate waters (zero-P intercept at − 0.23 nmol Cd kg−1). The lowest Cd concentrations were observed in subtropical waters north of the STC. Here the Cd-P slope was only 0.08 × 10−3 mol Cdmol P, indicating that the Cd-P properties in this region are dominated by mixing of low-Cd, high-P subantarctic water across the STC. Freshwater sources of Cd and P were found to be negligible. This work implies that the northern region of the Southern Ocean plays a major role in the global Cd-P relationship. Two mechanisms are suggested: (1) the ventilation of low-Cd-P subantarctic water to intermediate depth through Antarctic Intermediate Water formation, and (2) the remineralisation of low-Cd-P detritus from biota produced in waters formed at the STC.

Physical mixing effects on iron biogeochemical cycling: FeCycle experiment

The effects of physical processes on the distribution, speciation, and sources/sinks for Fe in a high-nutrient low-chlorophyll (HNLC) region were assessed during FeCycle, a mesoscale SF6 tracer release during February 2003 (austral summer) to the SE of New Zealand. Physical mixing processes were prevalent during FeCycle with rapid patch growth (strain rate γ = 0.17–0.20 d−1) from a circular shape (50 km2) into a long filament of ∼400 km2 by day 10. Slippage between layers saw the patch-head overlying noninfused waters while the tail was capped by adjacent surface waters resulting in a SF6 maximum at depth. As the patch developed it entrained adjacent waters containing higher chlorophyll concentrations, but similar dissolved iron (DFe) levels, than the initial infused patch. DFe was low ∼60 pmol L−1 in surface waters during FeCycle and was dominated by organic complexation. Nighttime measurements of Fe(II) ∼20 pmol L−1 suggest the presence of Fe(II) organic complexes in the absence of an identifiable fast Fe(III) reduction process. Combining residence times and phytoplankton uptake fluxes for DFe it is cycled through the biota 140–280 times before leaving the winter mixed layer (WML). This strong Fe demand throughout the euphotic zone coupled with the low Fe:NO3 − (11.9 μmol:mol) below the ferricline suggests that vertical diffusion of Fe is insufficient to relieve chronic iron limitation, indicating the importance of atmospheric inputs of Fe to this region.