Search results | Digital Commons of Moss Landing Marine Laboratories

Title: Distribution and enrichment of trace metals in marine sediments from the Eastern Equatorial Atlantic, off the coast of Ghana in the Gulf of Guinea
Description: We present results of a preliminary geochemical assessment of Cd, Pb, V, As, Ni, Cu, Zn, Mg, Al, K, Ca, and Fe in marine sediments from the Eastern Equatorial Atlantic, off the Coast of Ghana. Samples were taken along 4 regions G1, G2, G3 and G4 at approximately 25 m, 100 m, and 250 m, 500 m and 1000 m depths. Elemental compositions were assessed through the estimation of Al-normalized enrichment factors and geochemical accumulation indices, and the concentrations determined to produce any potential toxic effects to biota. Significant enrichment of the bottom sediments with Cd, Ni and As were observed at some locations with sediments showing signs of heavy pollution with As at region 4. Apart from Ni, V and As which were beyond threshold levels at most regions, all other metals were below probable effect levels. Both natural and anthropogenic processes controlled trace metal accumulation and distribution in the Ghanian coastal environment., Rocks and Cores, Oceanography, In press
Author: Mahu, Nyarko, Hulme, Coale
Date: 2015-01-01T00:00:00Z

Title: Copper complexation in the Northeast Pacific,
Description: Copper titrations were conducted at sea with differential pulse anodic stripping voltammetry to examine the degree to which copper was associated with organic ligands. Greater than 99.7% of the total dissolved copper in surface waters of the central Northeast Pacific shallower than 200 m was estimated to be associated with strong organic complexes. Below 200 m, increasing proportions of inorganic or labile copper species were observed. At middepths (1000 m), about 50-70% of the total dissolved copper was in the organically complexed form. Whereas total copper varies by a factor of only three from the surface to middepths (0.6-1.8 nM), copper complexation gives rise to extremely low cupric ion activities in surface waters ({Cu2+} = 1.4 × 10-4 M) and higher values at middepth ({Cu2+} = 10-11 M) -a variation of three orders of magnitude., Cited By (since 1996):208 Oceanography, ,
Author: Coale, Bruland
Date: 1988-01-01T00:00:00Z

Title: A massive phytoplankton bloom induced by an ecosystem-scale iron fertilization experiment in the equatorial Pacific Ocean
Description: 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., Cited By (since 1996):930, Oceanography
Author: Coale, Johnson, Fitzwater, Gordon, Tanner, Chavez, Ferioli, Sakamoto, Rogers, Millero, Steinberg, Nightingale, Cooper, Cochlan, Landry, Constantinou, Rollwagen, Trasvina, Kudela
Date: 1996-01-01T00:00:00Z

Title: Spatial and temporal variability in copper complexation in the North Pacific,
Description: The complexation of trace metals by organic ligands has long been proposed to play a significant role in determining trace metal speciation in seawater. However, analytical methodologies with sufficient specificity and sensitivity only recently have been developed to enable us to address questions of trace metal/organic complexation. In this study copper titrations were conducted at sea using differential pulse anodic stripping voltammetry on North Pacific samples to determine the extent of copper complexation with organic ligands. This study includes data from a transect from 33°N, 139°W to 55°N, 148°W and seasonal occupations of the VERTEX T-4 station (33°N, 139°W). The data indicate the presence of at least two copper binding ligands: L1, the stronger ligand, or ligand class, averages 2 nM with log K′l cond(Cu′) = 11.6; L2, the weaker ligand class varies between 5 and 10 nM witgh log K′2 cond(Cu′) = 8.6. The presence of these ligands strongly buffers the activity of copper(II) in surface waters at all stations. Seasonal variations in the distribution of strong copper complexing ligands follow seasonal variations in the depth of the mixed layer at T-4 and indicate a ligand source in the lower mixed layer. Ligand concentrations do not covary with the rates of primary productivity in a latitudinal transect from the central North Pacific to the subarctic. Ligand concentrations at all stations vary only by a factor of two and hold surface water copper(II) ion activities relatively constant (about 10-14 M), suggestive of a regulated ligand production mechanism. These results comprise a unique data set for copper complexation in the Pacific and may have significantly implications for the distribution of plankton between oligotrophic and subarctic systems. © 1990., Cited By (since 1996):113, Oceanography, ,
Author: Coale, Bruland
Date: 1990-01-01T00:00:00Z

Title: Spectrophotometric determination of dissolved manganese in natural waters with 1-(2-pyridylazo)-2-naphthol: Application to analysis in situ in hydrothermal plumes,
Description: A spectrophotometric method using the complexing reagent 1-(2-pyridylazo)-2-naphthol (PAN) was developed for the determination of dissolved manganese in seawater. A detection limit of approximately 22 nM was obtained when the analyses were performed in situ with a submersible chemical analyzer (Scanner). Color formation was rapid (less than 1 s), which permitted the technique to be used in flow injection and continuous flow systems. An investigation of possible interferences revealed that the only significant interferent to manganese determinations in seawater (hydrothermal plumes) was iron. The iron-specific chelating agent desferrioxamine B was used to mask this interference. Temperature and pressure did not adversely affect the sensitivity of the technique, which made it amenable to applications in situ to depths of 3000 m. This method was tested by measuring dissolved manganese concentrations in situ in submarine hydrothermal plumes using a Scanner. Scanner deployments over the Juan de Fuca Ridge produced the first near real time analyses of manganese from a hydrothermal plume environment. Estuarine samples have also been successfully analyzed in the laboratory and the results confirmed by an independent method. © 1992., Cited By (since 1996):22, Oceanography, CODEN: MRCHB, ,
Author: Chin, Johnson, Coale
Date: 1992-01-01T00:00:00Z

Title: The behaviour of iron and other trace elements during the IronEx-I and PlumEx experiments in the Equatorial Pacific,
Description: Dissolved (< 0.4 μm) and particulate (0.4-5 μm and > 5 μm, leachable and refractory) trace elements were measured during the IronEx I and PlumEx experiments in October and November 1993 near the Galapagos Islands. Iron was measured in the enriched patch and at control stations over a 9 day period following fertilization. The dissolved iron was initially depleted at a rate that gave an iron half-life of 28-40 h. The loss rate gradually decreased, and dissolved iron concentrations did not decrease below about 0.25 nmol kg-1 throughout the experiment. These results were most consistent with a kinetic model that was second order in iron concentration for the scavenging removal of each iron fraction. Other trace elements measured did not change significantly either in concentration or partitioning during the IronEx I experiment. Biological production tracked iron concentrations over time, which suggests that productivity within the fertilized patch was regulated by the availability of iron. The PlumEx study consisted primarily of two transects, a meridional course to the east of the Galapagos Islands and a zonal section to the west. Surface dissolved iron was very low at all stations except those near the Galapagos Islands. Sections of trace metal and other properties distinctly confirm the upwelling of the Equatorial Undercurrent as it intersects the islands. This upwelling has a great effect on the surface distributions of the trace metals on the west side of the islands. Productivity within the mixed layer of this region is highly correlated with iron and nitrate. West of the islands highest productivity is found at stations with the highest iron. North of the Equatorial front, in nitrate-depleted waters, elevated iron concentrations do not enhance productivity., Cited By (since 1996):58, Oceanography, CODEN: DSROE, ,
Author: Gordon, Johnson, Coale
Date: 1998-01-01T00:00:00Z

Title: The flux of iron from continental shelf sediments,
Description: The flux of dissolved iron from sediments to the water column was measured with flux chambers along the California coast over a five-year period. High fluxes were observed from sediments on the continental shelf. The measured fluxes were an average of 75 times larger than flux values derived from pore-water iron gradients. The iron flux was significantly correlated with the oxidation of organic matter, which allows an extrapolation to the global shelf. The input from shelf sediments is at least as significant as the global input of dissolved iron from aerosols, which has been presumed to be the dominant external iron source. Evidence of this input is seen 100's of kilometers offshore where it can enable the high productivity of broad coastal regions seen in satellite images. Copyright 2004 by the American Geophysical Union., Cited By (since 1996):125, Oceanography, CODEN: GPRLA, ,
Author: Elrod, Berelson, Coale, Johnson
Date: 2004-01-01T00:00:00Z

Title: What controls dissolved iron concentrations in the world ocean?,
Description: Dissolved (<0.4 μm) iron has been measured in 354 samples at 30 stations in the North and South Pacific, Southern Ocean and North Atlantic by the Trace Metals Laboratory at Moss Landing Marine Laboratories. These stations are all more than 50 km from a continental margin. The global distribution of dissolved iron, which is derived from these profiles, is remarkable for several reasons. The dissolved iron profiles have a uniform shape with a nutrient-like profile at each station. Concentrations at the surface are all <0.2 nmol kg-1 and average 0.07 nmol kg-1. Below 500 m, the average concentration is 0.76 nmol kg-1. The largest value in the data set is 1.38 nmol kg-1. There is no inter-ocean fractionation, which is unique for an element with a nutrient-like profile. Published estimates of the iron residence time are on the order of 100 to 200 yr, indicative of rapid removal. Other elements with such short residence times are characterized by vertical profiles that decrease with depth and deep concentrations that decrease with age as water passes from the Atlantic to the Pacific. This is not the case for iron. The largest horizontal changes in dissolved iron are observed in gradients from the continental margin. There is only a factor of three difference between the minimum (0.4 nmol kg-1) and maximum (1.3 nmol kg-1) value in the data set at a depth near 750 m, where variability is at a maximum. The minimum concentrations are found at stations in the remote central Pacific and the maximum values occur at stations adjacent to the continental margin. The major source of iron in the deep sea is generally aeolian deposition. Integrated (surface to 500 m) concentrations of iron at each station are only weakly correlated with the aeolian iron deposition flux, however. This contrasts with other elements such as lead that also have strong atmospheric sources. These observations lead us to conclude that the nutrient-like profile is maintained by a mechanism that reduces the scavenging rate of dissolved iron at concentrations less than 0.6 nmol kg-1. This mechanism may be complexation by strong iron binding ligands, which have been found in both the Atlantic and Pacific at concentrations near 0.6 nM. This apparent solubility would act to diminish inter-ocean fractionation. It would allow a nutrient-like profile to develop before scavenging began to remove iron. In order to test the concept, we developed a numerical model to make quantitative predictions of dissolved iron concentrations from place to place. The dissolved iron source in the ocean interior is remineralization from sinking particulate organic matter. Scavenging removes dissolved iron only at concentrations greater than the apparent solubility. The only geographically variable parameter in the model is the export flux of carbon from the surface layer, which carries iron with it. The model generated dissolved iron profiles, based on measured or estimated values of the carbon export flux, are in remarkable agreement with the observed profiles at all stations from the North Atlantic through the Southern Ocean to the North Pacific., Cited By (since 1996):386, CODEN: MRCHB, Oceanography, , ,
Author: Johnson, Michael Gordon, Coale
Date: 1997-01-01T00:00:00Z

Title: Cadmium flux in Los Angeles/Long Beach harbours and at sites along the California continental margin,
Description: Fluxes of dissolved cadmium were measured in situ using benthic flux chambers at stations in Los Angeles/Long Beach harbour and at sites on the California continental margin. Cadmium fluxes ranged from -0.212 to 0.118 μmol m-2 d-1 indicating that Cd flux may either be into or out of sediments. Correlations between Cd flux and carbon oxidation rate and between carbon oxidation rate and sulfate reduction indicate that anaerobic microbial degradation was the major process controlling both the sign and the magnitude of cadmium fluxes at stations in Los Angeles and Long Beach harbours. A simple box model based on sediment fluxes and water column concentrations indicates cadmium has a residence time of 47 days within the Los Angeles/Long Beach harbour system, similar to the hydraulic residence time. Sedimentary flux is, therefore, sufficient to account for water column cadmium concentration in inner harbour areas, suggesting that the sediments are the dominant source and sink of cadmium in these areas of the harbour. Comparison of the cadmium: phosphate ratio for the Los Angeles/Long Beach harbour water column with those reported for the northeast Pacific suggests that distributions of Cd in the study area were elevated over expected values but appear to be dominated by natural physical and biogeochemical processes. © 2001 Academic Press., Cited By (since 1996):9, Oceanography, CODEN: ECSSD, ,
Author: Colbert, Coale, Berelson, Johnson
Date: 2001-01-01T00:00:00Z

Title: Direct ultraviolet spectrophotometric determination of total sulfide and iodide in natural waters,
Description: A technique is described that allows the determination of total dissolved sulfide in natural waters using direct ultraviolet detection of the HS- ion. The concentration of bisulfide is determined by measuring absorption from 214 to 300 nm and then deconvolution of the HS- spectra from the complex spectrum of natural fluids. A nonlinear least-squares fitting approach is used for the deconvolution. At a pH near 8, where >95% of total sulfide is present as HS-, the results are indistinguishable from total sulfide measured using the methylene blue method in a wide range of sample types and matrixes including freshwater from groundwater wells, marine hydrothermal vent fluids, and marine sediment porewaters. The method allows simultaneous determination of other UV-absorbing ions, including nitrate, bromide, and iodide, in samples with low total sulfide concentrations. Bisulfide concentrations can be determined in samples with low background absorption, such as well water and hydrothermal fluids, with a detection limit of <1 μM. The detection limit for bisulfide in sediment porewaters that have a high organic loading, which produces background absorbances of ∼0.5 A at 260 nm in a 1-cm cuvette, is 5 μM. The only chemical manipulation required is buffering acidic samples to pH > 7 and filtration of particulate-rich samples., Cited By (since 1996):36, Oceanography, CODEN: ANCHA, ,
Author: Guenther, Johnson, Coale
Date: 2001-01-01T00:00:00Z

Title: Manganese flux from continental margin sediments in a transect through the oxygen minimum,
Description: The flux of manganese from continental margin sediments to the ocean was measured with a free-vehicle, benthic flux chamber in a transect across the continental shelf and upper slope of the California margin. The highest fluxes were observed on the shallow continental shelf. Manganese flux decreased linearly with bottom water oxygen concentration, and the lowest fluxes occurred in the oxygen minimum zone (at a depth of 600 to 1000 meters). Although the flux of manganese from continental shelf sediments can account for the elevated concentrations observed in shallow, coastal waters, the flux from sediments that intersect the oxygen minimum cannot produce the subsurface concentration maximum of dissolved manganese that is observed in the Pacific Ocean., Cited By (since 1996):47, Oceanography, CODEN: SCIEA, ,
Author: Johnson, Berelson, Coale, Coley, Elrod, Fairey, Iams, Kilgore, Nowicki
Date: 1992-01-01T00:00:00Z

Title: Spatial and habitat-rased variations in total and methyl mercury concentrations in surficial sediments in the San Francisco Bay-Delta,
Description: Recent studies indicate significant amounts of mercury (Hg) are annually transported into the San Francisco Bay-Delta (Bay-Delta) as a result of historic gold and Hg mining activities. We examined temporal and spatial variation in concentrations of total Hg (HgT) and monomethylmercury (MMHg) in surficial sediments of various ecosystem types in the Bay-Delta. We sampled surficial sediments across the Bay-Delta system and found HgT sediment concentrations in the central Delta were generally 100-200 ng g -1 and increased westward through Suisun Bay to 250-350 ng g -1. MMHg concentrations in the central Delta were between 1 and 3 ng g-1, while those in sediments in the perimeter waterways and adjacent bays were less than 1 ng g-1. Six sites were monitored monthly for over a year to identify seasonal changes in Hg sediment concentrations. Hg T sediment concentrations ranged from 48 to 382 ng g-1 and varied as a function of location not season. However, MMHg concentrations varied seasonally, increasing from 1 ng g-1 during winter months to 6 ng g-1 during spring and summer. Transects conducted at three marshes in the central Delta revealed MMHg sediment concentrations of 4-8 ng g-1at the interior and 2 ng g-1 at the exterior of the marshes. Habitat type was a major factor controlling MMHg concentration and the MMHg to HgT ratio in sediments of the Bay-Delta. MMHg was significantly correlated to HgT (r2 = 0.49) in marsh sediments. © 2007 American Chemical Society., Cited By (since 1996):24, Oceanography, CODEN: ESTHA, ,
Author: Heim, Coale, Stephenson, Choe, Gill, Foe
Date: 2007-01-01T00:00:00Z

Title: Effect of iron limitation on the cadmium to phosphorus ratio of natural phytoplankton assemblages from the Southern Ocean,
Description: There is considerable interest in the biogeochemical cycling of cadmium (Cd) and phosphate (PO 4) in surface waters, driven in part by the ongoing development of a paleonutrient proxy that utilizes Cd preserved in fossil planktonic foraminifera to determine past PO 4 utilization efficiencies in ocean surface waters. The present article reports the results of a field study into the effects of Fe limitation on the Cd:P composition of natural assemblages of marine phytoplankton in the Antarctic Zone of the Pacific sector of the Southern Ocean. Iron enrichment to shipboard incubation bottles led to increases in community growth rate and final biomass. After 10.7 d of incubation, the climax community was dominated by large diatoms of the genus Fragillariopsis, Pseudonitzschia, and Nitzschia. Direct measurements of phytoplankton metal : P ratios from controlled shipboard experiments indicate that Cd:P, Co:P, and Zn:P ratios decreased from control values with increasing initial dissolved Fe concentrations in the incubation bottles, by factors of ∼2-10 at highest Fe additions. We suggest that the effect of Fe limitation on resident diatoms is to decrease growth rate, leading to elevated cellular Cd content. The dissolved Cd:P ratio in iron-limited surface waters of the Southern Ocean may, therefore, respond to the supply of Fe to the resident phytoplankton community, which has implications for the developing paleonutrient proxy. We suggest that the biological uptake of Cd and P is independent of the dissolved Cd:PO 4 ratio. As a consequence, the results argue against the use of empirical Rayleigh fractionation models or models with fixed phytoplankton uptake ratios to account for regional variability in surface water dissolved Cd:PO 4., Cited By (since 1996):33, Oceanography, CODEN: LIOCA, ,
Author: Cullen, Chase, Coale, Fitzwater, Sherrell
Date: 2003-01-01T00:00:00Z

Title: Analytical chemistry in oceanography,
Description: Cited By (since 1996):41, Oceanography, CODEN: ANCHA, , ,
Author: Johnson, Coale, Jannasch
Date: 1992-01-01T00:00:00Z

Title: Accumulation rate and mixing of shelf sediments in the Monterey Bay National Marine Sanctuary,
Description: The distribution of excess 210Pb in 31 sediment cores was used to determine modern (last 100 yr) mass accumulation rates and the depth of sediment mixing on the continental shelf between Pacifica and Monterey, California, USA. Apparent mass accumulation rates average 0.27 g cm-2 yr-1 and range from 0.42 g cm-2 yr-1 to 0.12 g cm-2 yr-1. Accumulation rates were highest at mid-shelf water depths (60-100 m) adjacent to major rivers and near the head of the Ascension submarine canyon. Cores from water depths of less than 65 m had low, uniform 210Pb activity profiles and sandy textures. The uppermost 5-13 cm of 15 cores had uniform 210Pb activity profiles above a region of steadily decreasing 210Pb activity. This phenomenon was attributed to sediment mixing. The thickness of this upper layer of uniform 210Pb activity decreased southward from 13 cm, west of Pacifica, to less than 5 cm, near Monterey Canyon. This southward decrease may be attributed to shallower bioturbation in the southern study area. Integrated excess 210Pb activities were generally higher where sedimentation rates were high. They were also higher with increasing distance from major rivers. Thus, sedimentation rate alone does not explain the distribution of integrated excess 210Pb in this study area. Excess 210Pb in the seafloor is controlled by other factors such as sediment texture, the atmospheric deposition rate of 210Pb, and the residence time of sediment particles in the water column. © 2002 Elsevier Science B.V. All rights reserved., Cited By (since 1996):28, CODEN: MAGEA, , , Oceanography
Author: Lewis, Coale, Edwards, Marot, Douglas, Burton
Date: 2002-01-01T00:00:00Z

Title: Sediment-water exchange of total mercury and monomethyl mercury in the San Francisco Bay-Delta,
Description: Five field trips were conducted in the San Francisco Bay-Delta between May 2000 and October 2001 to investigate the sediment-water exchange of total mercury (Hg) and monomethyl mercury (MMHg). Solid-phase Hg averaged ∼1 nmol g -1 and did not show any variability with depth or time or among sites. In contrast, solid-phase MMHg showed considerable vertical, temporal, and spatial variability (0.4-66 pmol g -1), with the highest values occurring at a peat-rich environment in May 2001, suggesting that MMHg production was largely controlled by temporal factors and habitat type. In pore water, both Hg and MMHg concentrations were generally elevated near the sediment-water interface during warm months. Sediment-water exchange flux of MMHg, determined with benthic chamber deployments, ranged from -92 to 850 pmol m -2 d -1, with higher values occurring in May. In most cases, diffusional fluxes of Hg and MMHg, estimated with the use of interfacial concentration gradients, constituted only a minor portion of the measured fluxes, suggesting the importance of advective processes on sediment-water exchange. Surface-water transect and time series studies conducted in Franks Tract support the commonly held belief that wetland and marsh regions are major sources for MMHg within the Delta. The integrated sediment-water fluxes of Hg and MMHg in the study area were estimated to be 130 and 6 mmol d -1, respectively, and the benthic input was as important a source of Hg and MMHg as the riverine input within the Delta during low-flow months., Cited By (since 1996):63, Rocks and Cores, Oceanography, CODEN: LIOCA, ,
Author: Choe, Gill, Lehman, Han, Heim, Coale
Date: 2004-01-01T00:00:00Z

Title: A switch from Si(OH)4 to NO- 3 depletion in the glacial Southern Ocean,
Description: Phytoplankton in the Antarctic deplete silicic acid (Si(OH)4) to a far greater extent than they do nitrate (NO3 -). This pattern can be reversed by the addition of iron which dramatically lowers diatom Si(OH)4:NO3 - uptake ratios. Higher iron supply during glacial times would thus drive the Antarctic towards NO3 - depletion with excess Si(OH)4 remaining in surface waters. New δ30Si and δ15N records from Antarctic sediments confirm diminished Si(OH)4 use and enhanced NO3 - depletion during the last three glaciations. The present low-Si(OH)4 water is transported northward to at least the subtropics. We postulate that the glacial high-Si(OH)4 water similarly may have been transported to the subtropics and beyond. This input of Si(OH)4 may have caused diatoms to displace coccolithophores at low latitudes, weakening the carbonate pump and increasing the depth of organic matter remineralization. These effects may have lowered glacial atmospheric pCO2 by as much as 60 ppm., Cited By (since 1996):108, CODEN: GPRLA, , , Oceanography, Antarctica
Author: Brzezinski, Pride, Franck, Sigman, Sarmiento, Matsumoto, Gruber, Rau, Coale
Date: 2002-01-01T00:00:00Z

Title: The distribution and behavior of dissolved and particulate iron and zinc in the Ross Sea and Antarctic circumpolar current along 170°W,
Description: Dissolved and particulate iron and zinc were measured in water samples collected from the Antarctic Circumpolar Current (ACC) region and the Ross Sea during the US JGOFS Antarctic Environment Southern Ocean Process Study (AESOPS). Dissolved and particulate zinc showed strongly seasonal variation, indicating efficient recycling in the upper 150 m of the water column in both regions. Seasonal zinc utilization is 21-118 μmol m-2 in the ACC and 134-192 μmol m-2 in the Ross Sea. Only 10-25% of the particulate zinc is exported below 150 m. Generally low dissolved (<0.05 nmol kg -1) and particulate iron concentrations (<0.2 nmol kg -1) were observed in the mixed layer year-around in the ACC region whereas seasonal depletion of dissolved iron and relatively high particulate iron (>1 nmol kg-1) were found in the Ross Sea. Seasonal iron utilization is 7-45 μmol m-2 in the ACC and 450-938 μmol m -2 in the Ross Sea, which yields an estimated Fe/C ratio of 15 and 100 (μmol Fe:mol C) for the ACC and the Ross Sea, respectively. More than 50% of the total iron production is exported below 150 m in the ACC region. Iron input through vertical mixing was minimal, in contrast to the vertical input of dissolved zinc and macronutrients in the ACC region. Upwelling may supply 50% of the export production of iron near the Southern ACC Front. In the Ross Sea, more iron is available due to the variety of inputs, in contrast to the ACC region. In addition to the input of dissolved and particulate iron from melting sea-ice, there is substantial input of particulate iron from the suspended materials of sediments. © 2004 Elsevier Ltd. All rights reserved., Cited By (since 1996):42, Oceanography, CODEN: DRORE, Antarctica, ,
Author: Coale, Gordon, Wang
Date: 2005-01-01T00:00:00Z

Title: A rosette system for the collection of trace metal clean seawater,
Description: We designed a large-volume rosette sampler for collecting seawater with minimal trace metal contamination. The system uses eight modified 30-liter Go-Flo bottles secured to a Nylon II-coated stainless steel frame. The instrument is deployed with a dedicated winch with polyurethane-coated, three-conductor Kevlar hydroline. A prototype was used as part of the U.S. JGOFS Equatorial Pacific sampling program during spring and fall 1992. A redesigned model was used during the 1993 IronEx experiments and is currently being deployed in the Arabian Sea. The results of trace metal analyses collected on these cruises indicate that samples recovered are comparable to current single Go-Flo casts., Cited By (since 1996):28, CODEN: LIOCA, , , Oceanography, Downloaded from: www.aslo.org/lo/toc/vol_41/issue_6/1367.pdf (23 June 2014).
Author: Hunter, Gordon, Fitzwater, Coale
Date: 1996-01-01T00:00:00Z

Title: Synthesis of iron fertilization experiments: From the iron age in the age of enlightenment,
Description: 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. Copyright 2005 by the American Geophysical Union., Cited By (since 1996):271, Oceanography, Art. No.: C09S16, , , Downloaded from: http://onlinelibrary.wiley.com/doi/10.1029/2004JC002601/pdf (16 June 2014).
Author: de Baar, Boyd, Coale, Landry, Tsuda, Assmy, Bakker, Bozec, Barber, Brzezinski, Buesseler, Boyé, Croot, Gervais, Gorbunov, Harrison, Hiscock, Laan, Lancelot, Law, Levasseur, Marchetti, Millero, Nishioka, Nojiri, van Oijen, Riebesell, Rijkenberg, Saito, Takeda, Timmermans, Veldhuis, Waite, Wong
Date: 2005-01-01T00:00:00Z