Thorium-234 as a tracer of spatial,temporal and vertical variability in particle flux in the North Pacific     

K.O. Buesseler  S. Pike  K. Maiti  C.H. Lamborg  D.A. Siegel  T.W. Trull 《Deep Sea Research Part I: Oceanographic Research Papers》2009,56(7):1143-1167

An extensive ²³⁴Th data set was collected at two sites in the North Pacific: ALOHA, an oligotrophic site near Hawaii, and K2, a mesotrophic HNLC site in the NW Pacific as part of the VERTIGO (VERtical Transport In the Global Ocean) study. Total ²³⁴Th:²³⁸U activity ratios near 1.0 indicated low particle fluxes at ALOHA, while ²³⁴Th:²³⁸U ～0.6 in the euphotic zone at K2 indicated higher particle export. However, spatial variability was large at both sites—even greater than seasonal variability as reported in prior studies. This variability in space and time confounds the use of single profiles of ²³⁴Th for sediment trap calibration purposes. At K2, there was a decrease in export flux and increase in ²³⁴Th activities over time associated with the declining phase of a summer diatom bloom, which required the use of non-steady state models for flux predictions. This variability in space and time confounds the use of single profiles of ²³⁴Th for sediment trap calibration purposes. High vertical resolution profiles show narrow layers (20–30 m) of excess ²³⁴Th below the deep chlorophyll maximum at K2 associated with particle remineralization resulting in a decrease in flux at depth that may be missed with standard sampling for ²³⁴Th and/or with sediment traps. Also, the application of ²³⁴Th as POC flux tracer relies on accurate sampling of particulate POC/²³⁴Th ratios and here the ratio is similar on sinking particles and mid-sized particles collected by in-situ filtration (>10–50 μm at ALOHA and >5–350 μm at K2). To further address variability in particle fluxes at K2, a simple model of the drawdown of ²³⁴Th and nutrients is used to demonstrate that while coupled during export, their ratios in the water column will vary with time and depth after export. Overall these ²³⁴Th data provide a detailed view into particle flux and remineralization in the North Pacific over time and space scales that are varying over days to weeks, and 10's–100's km at a resolution that is difficult to obtain with other methods.  相似文献   

Dissolved iron in the Australian sector of the Southern Ocean (CLIVAR SR3 section): Meridional and seasonal trends     

P.N. Sedwick  A.R. Bowie  T.W. Trull   《Deep Sea Research Part I: Oceanographic Research Papers》2008,55(8):911-925

We report measurements of dissolved iron (dFe, <0.4 μm) in seawater collected from the upper 300 m of the water column along the CLIVAR SR3 section south of Tasmania in March 1998 (between 42°S and 54°S) and November–December 2001 (between 47°S and 66°S). Results from both cruises indicate a general north-to-south decrease in mixed-layer dFe concentrations, from values as high as 0.76 nM in the Subtropical Front to uniformly low concentrations (<0.1 nM) between the Polar Front and the Antarctic continental shelf. Samples collected from the seasonal sea-ice zone in November–December 2001 provide no evidence of significant dFe inputs from the melting pack ice, which may explain the absence of pronounced ice-edge algal blooms in this sector of the Southern Ocean, as implied by satellite ocean-color images. Our data also allow us to infer changes in the dFe concentration of surface waters during the growing season. South of the Polar Front, a comparison of near-surface with subsurface (150 m depth) dFe concentrations in November–December 2001 suggests a net seasonal biological uptake of at least 0.14–0.18 nM dFe, of which 0.05–0.12 nM is depleted early in the growing season (before mid December). A comparison of our spring 2001 and fall 1998 data indicates a barely discernible seasonal depletion of dFe (0.03 nM) within the Polar Frontal Zone. Further north, most of our iron profiles do not exhibit near-surface depletions, and mixed-layer dFe concentrations are sometimes higher in samples from fall 1998 compared to spring 2001; here, the near-surface dFe distributions appear to be dominated by time-varying inputs of aerosol iron or advection of iron-rich subtropical waters from the north.  相似文献   

Metals in eggs and hatchlings of Dermochelys coriacea (testudines) in Espírito Santo,Brazil and their relation to hatching and emergence success     

Jordana Borini Freire  Rafael M. Sousa  Karla Taufner  Maria TW Carneiro  Henrique R Filgueiras  Dominik Lenz  Paulo Dias Ferreira  Denise C Endringer 《Marine Ecology》2021,42(1):e12633

Certain concentration of metal may influence survival in embryonic stages, reducing the birthrate and hatching emergence. This study aimed to evaluate concentration of metal in eggs and hatchlings of Dermochelys coriacea and correlate metal concentrations in eggs with hatching and emergence success. The samples were collected at Biological Reserve Station, ES, Brazil. At the nests' opening, unhatched eggs and stillborn hatchlings were collected to survey the successful hatching and emergence of D. coriacea. The eggs shell, egg content, and dead hatchlings metal concentrations were compared to hatching and emergence success. A positive correlation was found between the concentration of copper (Cu) in the hatchlings and the success of the emergence (r² = .28, p < .05), and a moderate positive correlation between the concentrations of iron (Fe) and barium (Ba; r² = .44, p < .05) and success hatching. The concentrations of metals in eggs and hatchlings of D. coriacea in the Espírito Santo are below the levels that could be considered harmful to the species. In summary, there is a positive correlation between metals levels and hatching and emergence success.  相似文献   

Understanding the export of biogenic particles in oceanic waters: Is there consensus?     

P.W. Boyd  T.W. Trull 《Progress in Oceanography》2007,72(4):276-312

We examine progress towards a global view of oceanic export of particulate organic carbon (POC) and other nutrient elements (P, N, Si) from the surface (upper 100 m), through the subsurface, to the deep sea (>1000 m), focusing on syntheses published since 1999 and on the Joint Global Ocean Flux Study. Food-web structure is important, and surface and subsurface processes contribute similarly to determine the fraction of net primary production (NPP) reaching the deep sea. NPP by large cells generally favours high surface export of POC. Preferential remineralization of P and N (versus C) with depth is common, as is regional variation in subsurface POC flux attenuation.The role of mineral fluxes is complex. Annual mean fluxes of POC and minerals are correlated in global deep sediment trap records, but causality and the relative importance of different minerals depends on the assumptions made. Time-series observations at single sites can oppose the geographic trends, and their large seasonal variability in the contribution of POC to total flux is at odds with mechanistic models for POC transport by minerals. Despite generally positive correlations between biogenic carbonate and POC fluxes, the overall role of carbonate export is to decrease the transfer of carbon dioxide from the atmosphere to the ocean. Both autotrophs and heterotrophs produce minerals, and progress in separating these contributions is required for the deconvolution of mineral ballast and food-web effects.Many recent models suggest global surface POC export of ∼10 GTC/yr, despite widely varying biological complexity. This limits the usefulness of their prediction of ecosystem and carbon cycle responses to global change. Progress requires better observations for model validation, and more efforts to relate the models to the observed complexity, rather than to overly simplified global syntheses. We advocate more time-series stations targeting under-studied biogeochemical regions, development of automated in situ tools for study of the subsurface ocean, and increased emphasis on combining ecological and biogeochemical methods.  相似文献   

Matching carbon pools and fluxes for the Southern Ocean Iron Release Experiment (SOIREE)     

Dorothee C.E. Bakker  Philip W. Boyd  Edward R. Abraham  Matthew A. Charette  Mark P. Gall  Julie A. Hall  Cliff S. Law  Scott D. Nodder  Karl Safi  Dick J. Singleton  Kim Tanneberger  Thomas W. Trull  Anya M. Waite  Andrew J. Watson  John Zeldis 《Deep Sea Research Part I: Oceanographic Research Papers》2006,53(12):1941-1960

The Lagrangian Southern Ocean Iron Release Experiment (SOIREE) allowed study of a gradually evolving iron-mediated phytoplankton bloom in water labelled with the inert tracer sulfur hexafluoride, SF₆. This article describes a pelagic carbon budget for the mixed layer in SOIREE and assesses the extent to which closure of the budget is achieved. Net community production (NCP) converted 837 mmol m⁻² of inorganic carbon to organic carbon in 12.0 d after the first iron addition. A large fraction (41%) of NCP remained as particulate organic carbon in the mixed layer of the iron-enriched patch, while 23% was lost by horizontal dispersion and 0–29% was exported. The closure of the carbon budget is hampered by the lack of measurements of dissolved organic carbon (DOC), by a major uncertainty in carbon export, and by use of empirical conversion factors in estimates of carbon biomass and metabolic rates. Lagrangian carbon-budget studies may be improved by direct measurement of all major carbon parameters and conversion factors. Carbon cycling in the SOIREE bloom resembled that in ‘natural’ algal blooms in the open Southern Ocean in some respects, but not in all. Daily NCP in the SOIREE bloom (70 mmol m⁻² d⁻¹) was higher than in natural blooms, partly because other studies did not account for horizontal dispersion, were for longer periods or included less productive areas. The build-up of POC stock and carbon export as a fraction of NCP in SOIREE were in the lower range of observations elsewhere.  相似文献   

An assessment of particulate organic carbon to thorium-234 ratios in the ocean and their impact on the application of Th as a POC flux proxy     

K.O. Buesseler  C.R. Benitez-Nelson  S.B. Moran  A. Burd  M. Charette  J.K. Cochran  L. Coppola  N.S. Fisher  S.W. Fowler  W.D. Gardner  L.D. Guo   . Gustafsson  C. Lamborg  P. Masque  J.C. Miquel  U. Passow  P.H. Santschi  N. Savoye  G. Stewart  T. Trull 《Marine Chemistry》2006,100(3-4):213

Thorium-234 is increasingly used as a tracer of ocean particle flux, primarily as a means to estimate particulate organic carbon export from the surface ocean. This requires determination of both the ²³⁴Th activity distribution (in order to calculate ²³⁴Th fluxes) and an estimate of the C / ²³⁴Th ratio on sinking particles, to empirically derive C fluxes. In reviewing C / ²³⁴Th variability, results obtained using a single sampling method show the most predictable behavior. For example, in most studies that employ in situ pumps to collect size fractionated particles, C / ²³⁴Th either increases or is relatively invariant with increasing particle size (size classes > 1 to 100s μm). Observations also suggest that C / ²³⁴Th decreases with depth and can vary significantly between regions (highest in blooms of large diatoms and highly productive coastal settings). Comparisons of C fluxes derived from ²³⁴Th show good agreement with independent estimates of C flux, including mass balances of C and nutrients over appropriate space and time scales (within factors of 2–3). We recommend sampling for C / ²³⁴Th from a standard depth of 100 m, or at least one depth below the mixed layer using either large volume size fractionated filtration to capture the rarer large particles, or a sediment trap or other device to collect sinking particles. We also recommend collection of multiple ²³⁴Th profiles and C / ²³⁴Th samples during the course of longer observation periods to better sample temporal variations in both ²³⁴Th flux and the characteristic of sinking particles. We are encouraged by new technologies which are optimized to more reliably sample truly settling particles, and expect the utility of this tracer to increase, not just for upper ocean C fluxes but for other elements and processes deeper in the water column.  相似文献   

Indices based on silicoflagellate assemblages offer potential for paleo-reconstructions of the main oceanographic zones of the Southern Ocean     

Andrés S. Rigual-Hernández  Thomas W. Trull  Kevin McCartney  Anne-Marie Ballegeer  Kelly-Anne Lawler  Stephen G. Bray  Leanne K. Armand 《Geo-Marine Letters》2016,36(4):271-280

This study reports detailed silicoflagellate assemblage composition and annual seasonal flux from sediment traps at four locations along a transect across the Southern Ocean frontal systems. The four traps sampled the central Subantarctic Zone (SAZ, 47°S site), the Subantarctic Front (SAF, 51°S site), the Polar Frontal Zone (54°S site) and the Antarctic Zone (61°S site) across the 140°E longitude. Annual silicoflagellate fluxes to the deep ocean exhibited a similar latitudinal trend to those of diatom fluxes reported in previous work, with maxima in the Antarctic Zone and minima in the Subantarctic Zone. The data suggest that, along with diatoms, silicoflagellates are important contributors to biogenic silica export at all sites, particularly in the Subantarctic Zone. Two main silicoflagellate genera were observed, with Stephanocha sp. (previously known as Distephanus) dominating polar waters and Dictyocha sp. important in sub-polar waters. This is consistent with previous use of the Dictyocha / Stephanocha ratio to infer paleotemperatures and monitor shifts in the position of the Polar Frontal Zone in the sedimentary record. It appears possible to further refine the application of this approach by using the ratio between two Dictyocha species, because Dictyocha aculeata dominated at the Subantarctic Front, while Dictyocha stapedia dominated in the central Subantarctic Front. Given the well-defined environmental affinities of both species, a new SAF silicoflagellate index (SAF-SI) based on this ratio is proposed as a useful diagnostic for SAF and SAZ water mass signatures in the Plio-Pleistocene and Holocene sedimentary record.  相似文献   

Annual cycle of fCO₂ under sea-ice and in open water in Prydz Bay, East Antarctica     

John A. E. Gibson  Tom W. Trull 《Marine Chemistry》1999,66(3-4)

The annual cycle of dissolved nutrients and the fugacity of CO₂ (fCO₂), calculated from the concentration of dissolved inorganic carbon (DIC) and pH, was studied over a 14-month long period (December 1993 to February 1995) at a site in Prydz Bay near Davis Station, Vestfold Hills, East Antarctica. Significant spring decreases in fCO₂ began under the sea-ice in mid-October, when both water column and sea-ice algal activity resulted in the removal of nutrients and DIC and increased pH. Minimum fCO₂ (<100 μatm) and lowest nutrient and DIC concentrations occurred in December and January. The low summer fCO₂ values were clearly the result of biological activity. The seasonal depletion of dissolved nitrate reached 85% in mid-summer when chlorophyll-a concentrations exceeded 15 mg m⁻³. Oceanic uptake of carbon dioxide from the atmosphere, calculated from the fugacity difference and daily wind speeds, averaged more than 30 mmol m⁻² day⁻¹ during the summer ice-free period. This exchange replaced approximately half of the DIC consumed by biological activity. Apparent nutrient utilisation ratios (C/N/P) were close to Redfield values. In autumn fCO₂ began to rise, continuing slowly well into winter, and reaching a maximum close to modern atmospheric values between July and September. This increase can be attributed to a combination of local remineralisation of organic carbon in the water column and the steady increase in the mixing depth of the water column. At first glance, this suggests that air–sea equilibration occurred in winter despite the sea-ice cover, perhaps by horizontal circulation from regions outside the pack ice, or through openings in the ice. However, the persistent 15 to 20% undersaturation of dissolved oxygen throughout the winter suggests an alternate explanation. The late winter fCO₂ level may represent a characteristic established by global circulation, so that as a result of increasing atmospheric CO₂ concentrations, these Antarctic waters are in transition from being a winter-time source of CO₂ to the atmosphere to becoming a sink. Our fCO₂ observations emphasize the need to address seasonal variations in assessing Antarctic contributions to the oceanic control of atmospheric CO₂.  相似文献