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Stukel, MR, Kelly TB, Aluwihare LI, Barbeau KA, Goericke R, Krause JW, Landry MR, Ohman MD.  2019.  The Carbon:(234)Thorium ratios of sinking particles in the California current ecosystem 1: relationships with plankton ecosystem dynamics. Marine Chemistry. 212:1-15.   10.1016/j.marchem.2019.01.003   AbstractWebsite

We investigated variability in the C:Th-234 ratio of sinking particles and its relationship to changing water column characteristics and plankton ecological dynamics during 29 Lagrangian experiments conducted on six cruises of the California Current Ecosystem Long-Term Ecological Research (CCE-LTER) Program. C:Th-234 ratios of sinking particles collected by a surface-tethered sediment trap ((CThST)-Th-:234) varied from 2.3 to 20.5 mu mol C dpm(-1) over a depth range of 47-150 m. C:Th-234(ST) was significantly greater (by a factor of 1.8) than C:Th-234 ratios of suspended > 51-mu m particles collected in the same water parcels with in situ pumps. C:Th-234 ratios of large (> 200-mu m) sinking particles also exceeded those of smaller sinking particles. C:Th-234(ST) decreased with depth from the base of the euphotic zone through the upper twilight zone. C:Th-234(ST) was positively correlated with several indices of ecosystem productivity including particulate organic carbon (POC) and chlorophyll (Chl) concentrations, mesozooplankton biomass, and the fraction of Chl > 20-mu m. Principal component analysis and multiple linear regression suggested that decaying phytoplankton blooms exhibited higher C:Th-234(ST) than actively growing blooms at similar biomass levels. C:Th-234(ST) was positively correlated with indices of the fractional contribution of fecal pellets in sediment traps when the proportion of fecal pellets was low in the traps, likely because of a correlation between mesozooplankton biomass and other indices of ecosystem productivity. However, when fecal pellets were a more important component of sinking material, C:Th-234(ST) decreased with increasing fecal pellet content. C:Th-234(ST) was also positively correlated with the Si:C ratio of sinking particles. Across the dataset (and across depths) a strong correlation was found between C:Th-234(ST) and the ratio of vertically-integrated POC to vertically-integrated total water column Th-234 (C-v:Th-234(tot)). A mechanistic one-layer, two-box model of thorium sorption and desorption was invoked to explain this correlation. Two empirical models (one using C-v:Th-234(tot); one using depth and vertically-integrated Chl) were developed to predict C:Th-234 ratios in this coastal upwelling biome. The former regression (log(10)(C:Th-234(ST)) = 0.43 x log(10)(C-v:Th-234(tot)) + 0.53) was found to also be a reasonable predictor for C:Th-234(ST) from diverse regions including the Southern Ocean, Sargasso Sea, Subarctic North Pacific, and Eastern Tropical North Pacific.

McQuaid, JB, Kustka AB, Obornik M, Horak A, McCrow JR, Karas BJ, Zheng H, Kindeberg T, Andersson AJ, Barbeau KA, Allen AE.  2018.  Carbonate-sensitive phytotransferrin controls high-affinity iron uptake in diatoms. Nature. 555:534-537.   10.1038/nature25982   AbstractWebsite

In vast areas of the ocean, the scarcity of iron controls the growth and productivity of phytoplankton(1,2). Although most dissolved iron in the marine environment is complexed with organic molecules(3), picomolar amounts of labile inorganic iron species (labile iron) are maintained within the euphotic zone(4) and serve as an important source of iron for eukaryotic phytoplankton and particularly for diatoms(5). Genome-enabled studies of labile iron utilization by diatoms have previously revealed novel iron responsive transcripts(6,7), including the ferric iron-concentrating protein ISIP2A(8), but the mechanism behind the acquisition of picomolar labile iron remains unknown. Here we show that ISIP2A is a phytotransferrin that independently and convergently evolved carbonate ion-coordinated ferric iron binding. Deletion of ISIP2A disrupts high-affinity iron uptake in the diatom Phaeodactylum tricornutum, and uptake is restored by complementation with human transferrin. ISIP2A is internalized by endocytosis, and manipulation of the seawater carbonic acid system reveals a second order dependence on the concentrations of labile iron and carbonate ions. In P. tricornutum, the synergistic interaction of labile iron and carbonate ions occurs at environmentally relevant concentrations, revealing that carbonate availability co-limits iron uptake. Phytotransferrin sequences have a broad taxonomic distribution(8) and are abundant in marine environmental genomic datasets(9,10), suggesting that acidification-driven declines in the concentration of seawater carbonate ions will have a negative effect on this globally important eukaryotic iron acquisition mechanism.

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King, AL, Barbeau KA.  2011.  Dissolved iron and macronutrient distributions in the southern California Current System. Journal of Geophysical Research-Oceans. 116   10.1029/2010jc006324   AbstractWebsite

The distribution of dissolved iron in the southern California Current System (sCCS) is presented from seven research cruises between 2002 and 2006. Dissolved iron concentrations were generally low in most of the study area (<0.5 nM), although high mixed layer and water column dissolved iron concentrations (up to 8 nM) were found to be associated with coastal upwelling, both along the continental margin and some island platforms. A significant supply of iron was probably not from a deep remineralized source but rather from the continental shelf and bottom boundary layer as identified in previous studies along the central and northern California coast. With distance offshore, dissolved iron decreased more rapidly relative to nitrate in a transition zone 10-250 km offshore during spring and summer, resulting in relatively high ratios of nitrate: dissolved iron. Higher nitrate: dissolved iron ratios could be the result of utilization and scavenging in addition to an overall lower supply of iron relative to nitrate in the offshore transition zones. The low supply of iron leads to phytoplankton iron limitation and a depletion in silicic acid relative to nitrate in the coastal upwelling and transition zones of the sCCS.

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Brzezinski, MA, Krause JW, Bundy RM, Barbeau KA, Franks P, Goericke R, Landry MR, Stukel MR.  2015.  Enhanced silica ballasting from iron stress sustains carbon export in a frontal zone within the California Current. Journal of Geophysical Research-Oceans. 120:4654-4669.   10.1002/2015jc010829   AbstractWebsite

Nutrient dynamics, phytoplankton rate processes, and export were examined in a frontal region between an anticyclone and a pair of cyclones 120 km off the coast in the southern California Current System (sCCS). Low silicic acid: nitrate ratios (Si:N) and high nitrate to iron ratios (N: Fe) characteristic of Fe-limiting conditions in the sCCS were associated with the northern cyclone and with the transition zone between the cyclones and the anticyclone. Phytoplankton growth in low-Si:N, high-N:Fe waters responded strongly to added Fe, confirming growth limitation by Fe of the diatom-dominated phytoplankton community. Low Si: N waters had low biogenic silica content, intermediate productivity, but high export compared to intermediate Si: N waters indicating increased export efficiency under Fe stress. Biogenic silica and particulate organic carbon (POC) export were both high beneath low Si: N waters with biogenic silica export being especially enhanced. This suggests that relatively high POC export from low Si: N waters was supported by silica ballasting from Fe-limited diatoms. Higher POC export efficiency in low Si: N waters may have been further enhanced by lower rates of organic carbon remineralization due to reduced grazing of more heavily armored diatoms growing under Fe stress. The results imply that Fe stress can enhance carbon export, despite lowering productivity, by driving higher export efficiency.

King, AL, Barbeau K.  2007.  Evidence for phytoplankton iron limitation in the southern California Current System. Marine Ecology-Progress Series. 342:91-103.   10.3354/meps342091   AbstractWebsite

Observations of phytoplankton iron limitation in the world's oceans have primarily been confined to high-nutrient, low-chlorophyll (HNLC) regimes, found in the western equatorial and subarctic Pacific, Southern Ocean, and coastal upwelling zones off California and Peru. We investigated the potential for phytoplankton iron limitation in coastal transition zones (50 to 200 km offshore) of the southern California Current System, a weak upwelling regime that is relatively low in nutrients (< 4 mu mol nitrate 1(-1)) and low in chlorophyll (< 1 mu g chl a 1(-1)). In grow-out incubation experiments conducted during summer, July 2003 and 2004, phytoplankton responded to nanomolar iron additions, despite the non-HNLC initial conditions, Observed changes in phytoplankton and nutrient parameters upon iron addition were significant, although markedly lower in amplitude relative to typical grow-out experiments in HNLC regimes. While we cannot disprove alternate explanations for the observed limitation of phytoplankton growth, such as a proximate grazing control, our results indicate that phytoplankton growth in the southern California Current System is, at times, limited by the supply of iron. Based on our findings and the results of previous studies in this region, we suggest that phytoplankton biomass is generally limited by the supply of nitrate, while iron, directly or indirectly, influences macronutrient utilization, community species composition, and phytoplankton spatial and temporal distribution.

I
Pizeta, I, Sander SG, Hudson RJM, Omanovic D, Baars O, Barbeau KA, Buck KN, Bundy RM, Carrasco G, Croot PL, Garnier C, Gerringa LJA, Gledhill M, Hirose K, Kondo Y, Laglera LM, Nuester J, Rijkenberg MJA, Takeda S, Twining BS, Wells M.  2015.  Interpretation of complexometric titration data: An intercomparison of methods for estimating models of trace metal complexation by natural organic ligands. Marine Chemistry. 173:3-24.   10.1016/j.marchem.2015.03.006   AbstractWebsite

With the common goal of more accurately and consistently quantifying ambient concentrations of free metal ions and natural organic ligands in aquatic ecosystems, researchers from 15 laboratories that routinely analyze trace metal speciation participated in an intercomparison of statistical methods used to model their most common type of experimental dataset, the complexometric titration. All were asked to apply statistical techniques that they were familiar with to model synthetic titration data that are typical of those obtained by applying state-of-the-art electrochemical methods - anodic stripping voltammetry (ASV) and competitive ligand equilibration-adsorptive cathodic stripping voltammetry (CLE-ACSV) - to the analysis of natural waters. Herein, we compare their estimates for parameters describing the natural ligands, examine the accuracy of inferred ambient free metal ion concentrations (]M-f]), and evaluate the influence of the various methods and assumptions used on these results. The ASV-type titrations were designed to test each participant's ability to correctly describe the natural ligands present in a sample when provided with data free of measurement error, i.e., random noise. For the three virtual samples containing just one natural ligand, all participants were able to correctly identify the number of ligand classes present and accurately estimate their parameters. For the four samples containing two or three ligand classes, a few participants detected too few or too many classes and consequently reported inaccurate 'measurements' of ambient [M-f]. Since the problematic results arose from human error rather than any specific method of analyzing the data, we recommend that analysts should make a practice of using one's parameter estimates to generate simulated (back-calculated) titration curves for comparison to the original data. The root-mean-squared relative error between the fitted observations and the simulated curves should be comparable to the expected precision of the analytical method and upon visual inspection the distribution of residuals should not be skewed. Modeling the synthetic, CLE-ACSV-type titration dataset, which comprises 5 titration curves generated at different analytical-windows or levels of competing ligand added to the virtual sample, proved to be more challenging due to the random measurement error that was incorporated. Comparison of the submitted results was complicated by the participants' differing interpretations of their task. Most adopted the provided 'true' instrumental sensitivity in modeling the CLE-ACSV curves, but several estimated sensitivities using internal calibration, exactly as is required for actual samples. Since most fitted sensitivities were biased low, systematic error in inferred ambient [M-f] and in estimated weak ligand (L-2) concentrations resulted. The main distinction between the mathematical approaches taken by participants lies in the functional form of the speciation model equations, with their implicit definition of independent and dependent or manipulated variables. In 'direct modeling', the dependent variable is the measured [M-f] (or I-p) and the total metal concentration ([M](T)) is considered independent In other, much more widely used methods of analyzing titration data - classical linearization, best known as van den Berg/Ruzic and isotherm fitting by nonlinear regression, best known as the langmuir or Gerringa methods - [M-f] is defined as independent and the dependent variable calculated from both [M](T) and [M-f]. Close inspection of the biases and variability in the estimates of ligand parameters and in predictions of ambient [M-f] revealed that the best results were obtained by the direct approach. Linear regression of transformed data yielded the largest bias and greatest variability, while non-linear isotherm fitting generated results with mean bias comparable to direct modeling, but also with greater variability. Participants that performed a unified analysis of ACSV titration curves at multiple detection windows for a sample improved their results regardless of the basic mathematical approach taken. Overall, the three most accurate sets of results were obtained using direct modeling of the unified multiwindow dataset, while the single most accurate set of results also included simultaneous calibration. We therefore recommend that where sample volume and time permit, titration experiments for all natural water samples be designed to include two or more detection windows, especially for coastal and estuarine waters. It is vital that more practical experimental designs for multi-window titrations be developed. Finally, while all mathematical approaches proved to be adequate for some datasets, matrix-based equilibrium models proved to be most naturally suited for the most challenging cases encountered in this work, i.e., experiments where the added ligand in ACSV became titrated. The ProMCC program (Omanovic et al., this issue) as well as the Excel Add-in based KINETEQL Multiwindow Solver spreadsheet (Hudson, 2014) have this capability and have been made available for public use as a result of this intercomparison exercise. (C) 2015 The Authors. Published by Elsevier B.V.

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Buck, KN, Moffett J, Barbeau KA, Bundy RM, Kondo Y, Wu JF.  2012.  The organic complexation of iron and copper: an intercomparison of competitive ligand exchange-adsorptive cathodic stripping voltammetry (CLE-ACSV) techniques. Limnology and Oceanography-Methods. 10:496-515.   10.4319/lom.2012.10.496   AbstractWebsite

Characterization of the speciation of iron and copper is an important objective of the GEOTRACES Science Plan. To incorporate speciation measurements into such a multinational program, standard practices must be adopted that allow data from multiple labs to be synthesized. Competitive ligand exchange-adsorptive cathodic stripping voltammetry (CLE-ACSV) is the primary technique employed for measuring metal-binding ligands and determining metal speciation in seawater. The determination of concentrations and conditional stability constants of metal-binding ligands is particularly challenging, as results can be influenced both by experimental conditions and interpretation of titration data. Here, we report an investigation between four laboratories to study the speciation of iron and copper using CLE-ACSV. Samples were collected on the GEOTRACES II intercomparison cruise in the North Pacific Ocean in May 2009 at 30 degrees N, 140 degrees W. This intercomparison was carried out shipboard and included an assessment of the viability of sample preservation by freezing. Results showed that consensus values could be obtained between different labs, but that some existing practices were problematic and require further attention in future work. A series of recommendations emerged from this study that will be useful in implementing multi-investigator programs like GEOTRACES.

P
Landry, MR, Ohman MD, Goericke R, Stukel MR, Barbeau KA, Bundy R, Kahru M.  2012.  Pelagic community responses to a deep-water front in the California Current Ecosystem: overview of the A-Front Study. Journal of Plankton Research. 34:739-748.   10.1093/plankt/fbs025   AbstractWebsite

In October 2008, we investigated pelagic community composition and biomass, from bacteria to fish, across a sharp frontal gradient overlying deep waters south of Point Conception, California. This northsouth gradient, which we called A-Front, was formed by the eastward flow of the California Current and separated cooler mesotrophic waters of coastal upwelling origin to the north, from warm oligotrophic waters of likely mixed subarcticsubtropical origin to the south. Plankton biomass and phytoplankton growth rates were two to three times greater on the northern side, and primary production rates were elevated 5-fold to the north. Compared with either of the adjacent waters, the frontal interface was strongly enriched and uniquely defined by a subsurface bloom of large diatoms, elevated concentrations of suspension-feeding zooplankton, high bioacoustical estimates of pelagic fish and enhanced bacterial production and phytoplankton biomass and photosynthetic potential. Such habitats, though small in areal extent, may contribute disproportionately and importantly to regional productivity, nutrient cycling, carbon fluxes and trophic ecology. As a general introduction to the A-Front study, we provide an overview of its design and implementation, a brief summary of major findings and a discussion of potential mechanisms of plankton enrichment at the front.

Kwasnik, M, Fuhrer K, Gonin M, Barbeau K, Fernandez FM.  2007.  Performance, resolving power, and radial ion distributions of a prototype nanoelectrospray ionization resistive glass atmospheric pressure ion mobility spectrometer. Analytical Chemistry. 79:7782-7791.   10.1021/ac071226o   AbstractWebsite

In this article, we describe and characterize a novel ion mobility spectrometer constructed with monolithic resistive glass desolvation and drift regions. This instrument is equipped with switchable corona discharge and nanoelectrospray ionization sources and a Faraday plate detector. Following description of the instrument, pulsing electronics, and data acquisition system, we examine the effects of drift gas flow rate and temperature, and of the aperture grid to anode distance on the observed resolving power and sensitivity. Once optimum experimental parameters are identified, different ion gate pulse lengths, and their effect on the temporal spread of the ion packet were investigated. Resolving power ranged from an average value of 50 ms/ms for a 400-mu s ion gate pulse, up to an average value of 68 ms/ms for a 100-mu s ion gate pulse, and a 26-cm drift tube operated at 383 V cm(-1). Following these experiments, the radial distribution of ions in the drift region of the spectrometer was studied by using anodes of varying sizes, showing that the highest ionic density was located at the center of the drift tube. Finally, we demonstrate the applicability of this instrument to the study of small molecules of environmental relevance by analyzing a commercially available siderophore, deferoxamine mesylate, in both the free ligand and Fe-bound forms. Ion mobility experiments showed a dramatic shift to shorter drift times caused by conformational changes upon metal binding, in agreement with previous reversed-phase liquid chromatography observations.

Hogle, SL, Dupont CL, Hopkinson BM, King AL, Buck KN, Roe KL, Stuart RK, Allen AE, Mann EL, Johnson ZI, Barbeau KA.  2018.  Pervasive iron limitation at subsurface chlorophyll maxima of the California Current. Proceedings of the National Academy of Sciences of the United States of America. 115:13300-13305.   10.1073/pnas.1813192115   AbstractWebsite

Subsurface chlorophyll maximum layers (SCMLs) are nearly ubiquitous in stratified water columns and exist at horizontal scales ranging from the submesoscale to the extent of oligotrophic gyres. These layers of heightened chlorophyll and/or phytoplankton concentrations are generally thought to be a consequence of a balance between light energy from above and a limiting nutrient flux from below, typically nitrate (NO3). Here we present multiple lines of evidence demonstrating that iron (Fe) limits or with light colimits phytoplankton communities in SCMLs along a primary productivity gradient from coastal to oligotrophic offshore waters in the southern California Current ecosystem. SCML phytoplankton responded markedly to added Fe or Fe/light in experimental incubations and transcripts of diatom and picoeukaryote Fe stress genes were strikingly abundant in SCML metatranscriptomes. Using a biogeochemical proxy with data from a 40-y time series, we find that diatoms growing in California Current SCMLs are persistently Fe deficient during the spring and summer growing season. We also find that the spatial extent of Fe deficiency within California Current SCMLs has significantly increased over the last 25 y in line with a regional climate index. Finally, we show that diatom Fe deficiency may be common in the subsurface of major upwelling zones worldwide. Our results have important implications for our understanding of the biogeochemical consequences of marine SCML formation and maintenance.

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King, AL, Buck KN, Barbeau KA.  2012.  Quasi-Lagrangian drifter studies of iron speciation and cycling off Point Conception, California. Marine Chemistry. 128:1-12.   10.1016/j.marchem.2011.11.001   AbstractWebsite

The distribution and speciation of dissolved Fe (dFe) were measured during four quasi-Lagrangian drogued drifter studies (similar to 4 d duration each) that were conducted in the southern California Current System in May 2006 and April 2007. Three of the four drifter studies were within the coastal upwelling regime and one drifter study was in a warm-core anticyclonic eddy. Incubation bottle experiments were also conducted to determine the degree of phytoplankton Fe limitation and to assess changes in the concentration of Fe-binding ligands. In the coastal upwelling drifter studies, in situ dFe (1.4-1.8 nM) and macronutrients were initially high and declined over time. Fe addition incubation experiments indicated that the phytoplankton community was not Fe limited at the beginning of the coastal upwelling drifter experiments (when mu M nitrate:nM dFe ratios were similar to 7-8). By the end of two of the three drifter studies (when mu M nitrate:nM dFe ratios were similar to 12-19), Fe addition resulted in larger nitrate and silicic acid drawdown, and larger accumulations in chlorophyll a, particulate organic carbon and nitrogen, and diatom and dinoflagellate-specific carotenoid pigments. Fe speciation was measured in situ in three of the four drifter studies with stronger L-1-type ligands found to be present in excess of dFe in all samples. In Fe speciation incubation experiments. L-1-type ligand production was observed in conjunction with phytoplankton growth under Fe-limiting conditions. The results presented here support and add a quasi-Lagrangian perspective to previous observations of dFe and macronutrient cycling over space and time within the California coastal upwelling regime, including Fe limitation within the phytoplankton community in this region and the biological production of Fe-binding ligands concomitant with Fe limitation. (C) 2011 Elsevier B.V. All rights reserved.

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Barbeau, K, Kujawinski EB, Moffett JW.  2001.  Remineralization and recycling of iron, thorium and organic carbon by heterotrophic marine protists in culture. Aquatic Microbial Ecology. 24:69-81.   10.3354/ame024069   AbstractWebsite

To characterize trace metal cycling in marine systems as mediated by heterotrophic protists, we conducted a series of laboratory experiments in 2-organism model systems consisting of bacteria and protistan grazers. Trace metal isotopes (Fe-59 and Th-234),C-14, and bulk organic carbon measurements were used to follow the chemical transformation of bacterial carbon and associated trace metals by several different grazer species. Results indicate that grazers were able to cause repartitioning of Th and regeneration of Fe from bacterial prey into the dissolved phase (<0.2 m), even in particle-rich laboratory cultures. For both Th and Fe, protist grazing led to the formation of relatively stable dissolved and colloidal metal-organic species. Metal/carbon ratios of the particle pool in some model systems with grazers were significantly altered, indicating a decoupling of trace metal and organic carbon cycling through the grazing process. Different protist species exhibited substantial variation (up to a factor of 10) in their ability to quantitatively remobilize trace metals from bacterial prey. The implications of these findings for trace metal cycling in marine systems are discussed.