The seeding of an expanse of surface waters in the equatorial Pacific Ocean with low concentrations of dissolved iron triggered a massive phytoplankton bloom which consumed large quantities of carbon dioxide and nitrate that these microscopic plants cannot fully utilize under natural conditions. These and other observations provide unequivocal support for the hypothesis that phytoplankton growth in this oceanic region is limited by iron bioavailability.

No abstract

The Southern Ocean Carbon and Climate Observations and Modeling (SOCCOM) program has begun deploying a large array of biogeochemical sensors on profiling floats in the Southern Ocean. As of February 2016, 86 floats have been deployed. Here the focus is on 56 floats with quality‐controlled and adjusted data that have been in the water at least 6 months. The floats carry oxygen, nitrate, pH, chlorophyll fluorescence, and optical backscatter sensors. The raw data generated by these sensors can suffer from inaccurate initial calibrations and from sensor drift over time. Procedures to correct the data are defined. The initial accuracy of the adjusted concentrations is assessed by comparing the corrected data to laboratory measurements made on samples collected by a hydrographic cast with a rosette sampler at the float deployment station. The long‐term accuracy of the corrected data is compared to the GLODAPv2 data set whenever a float made a profile within 20 km of a GLODAPv2 station. Based on these assessments, the fleet average oxygen data are accurate to 1 ± 1%, nitrate to within 0.5 ± 0.5 µmol kg−1, and pH to 0.005 ± 0.007, where the error limit is 1 standard deviation of the fleet data. The bio‐optical measurements of chlorophyll fluorescence and optical backscatter are used to estimate chlorophyll a and particulate organic carbon concentration. The particulate organic carbon concentrations inferred from optical backscatter appear accurate to with 35 mg C m−3 or 20%, whichever is larger. Factors affecting the accuracy of the estimated chlorophyll a concentrations are evaluated.

N 2 fixation has been understudied in marine environments outside of the subtropical and tropical oceans and where water temperatures are typically below 20-25uC. We identified nifH phylotypes and measured N 2 fixation rates under ambient conditions (maximum of 19uC) in water collected 750 km off the coast of California in oligotrophic waters of the North Pacific Ocean (34uN, 129uW). Near-surface N 2 fixation rates averaged 0.25 6 0.05 nmol N L 21 d 21 for 24 incubation bottles. Despite low ambient concentrations of iron (,0.1 nmol L 21 ) and phosphorus (,0.3 mmol L 21 ), N 2 fixation rates were unaffected by iron and phosphorus amendments. Using reverse transcription-quantitative polymerase chain reaction (RT-QPCR) methodology, we estimated transcript abundance and patterns of expression for several unicellular diazotrophs, including the group A phylotype, which showed the highest daily mRNA abundances. The N 2 -fixing assemblage extended to 60-80 m depth, well below the seasonal thermocline (40 m). The calculated areal N 2 fixation rate (15 mmol N m 22 d 21 ) was small compared with estimates from other regions of the Pacific; however, the estimated fixation rate was similar to other published results, suggesting that processes other than cellular growth rate may determine the abundance of unicellular diazotrophs. Despite the low N 2 fixation rates, the new nitrogen added to the euphotic zone by N 2 fixation could account for at least 10% of new production during the study period.

Dissolved organic nitrogen (DON) supports a significant amount of heterotrophic production in the ocean. Yet, to date, the identity and diversity of microbial groups that transform DON are not well understood. To better understand the organisms responsible for transforming high molecular weight (HMW)-DON in the upper ocean, isotopically labeled protein extract from Micromonas pusilla, a eukaryotic member of the resident phytoplankton community, was added as substrate to euphotic zone water from the central California Current system. Carbon and nitrogen remineralization rates from the added proteins ranged from 0.002 to 0.35 μmol C l − 1 per day and 0.03 to 0.27 nmol N l − 1 per day. DNA stable-isotope probing (DNA-SIP) coupled with high-throughput sequencing of 16S rRNA genes linked the activity of 77 uncultivated freeliving and particle-associated bacterial and archaeal taxa to the utilization of Micromonas protein extract. The high-throughput DNA-SIP method was sensitive in detecting isotopic assimilation by individual operational taxonomic units (OTUs), as substrate assimilation was observed after only 24 h. Many uncultivated free-living microbial taxa are newly implicated in the cycling of dissolved proteins affiliated with the Verrucomicrobia, Planctomycetes, Actinobacteria and Marine Group II (MGII) Euryarchaeota. In addition, a particle-associated community actively cycling DON was discovered, dominated by uncultivated organisms affiliated with MGII, Flavobacteria, Planctomycetes, Verrucomicrobia and Bdellovibrionaceae. The number of taxa assimilating protein correlated with genomic representation of TonB-dependent receptor (TBDR)-encoding genes, suggesting a possible role of TBDR in utilization of dissolved proteins by marine microbes. Our results significantly expand the known microbial diversity mediating the cycling of dissolved proteins in the ocean.