Huang Kuo-Fang

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Huang

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Kuo-Fang

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Testing models of thorium and particle cycling in the ocean using data from station GT11-22 of the U.S. GEOTRACES North Atlantic section

( 2016-03-31) Lerner, Paul ; Marchal, Olivier ; Lam, Phoebe J. ; Anderson, Robert F. ; Buesseler, Ken O. ; Charette, Matthew A. ; Edwards, R. Lawrence ; Hayes, Christopher T. ; Huang, Kuo-Fang ; Lu, Yanbin ; Robinson, Laura F. ; Solow, Andrew R.

Thorium is a highly particle-reactive element that possesses different measurable radio-isotopes in seawater, with well-constrained production rates and very distinct half-lives. As a result, Th has emerged as a key tracer for the cycling of marine particles and of their chemical constituents, including particulate organic carbon. Here two different versions of a model of Th and particle cycling in the ocean are tested using an unprecedented data set from station GT11-22 of the U.S. GEOTRACES North Atlantic Section: (i) 21 228;230;234Th activities of dissolved and particulate fractions, (ii) 228Ra activities, (iii) 234;238U activities estimated from salinity data and an assumed 234U/238U ratio, and (iv) particle concentrations, below a depth of 125 m. The two model versions assume a single class of particles but rely on different assumptions about the rate parameters for sorption reactions and particle processes: a first version (V1) assumes vertically uniform parameters (a popular description), whereas the second (V2) does not. Both versions are tested by fitting to the GT11-22 data using generalized nonlinear least squares and by analyzing residuals normalized to the data errors. We find that model V2 displays a significantly better fit to the data than model V1. Thus, the mere allowance of vertical variations in the rate parameters can lead to a significantly better fit to the data, without the need to modify the structure or add any new processes to the model. To understand how the better fit is achieved we consider two parameters, K = k1=(k-1 + β-1) and K/P, where k1 is the adsorption rate constant, k-1 the desorption rate constant, β-1 the remineralization rate constant, and P the particle concentration. We find that the rate constant ratio K is large (≥0.2) in the upper 1000 m and decreases to a nearly uniform value of ca. 0.12 below 2000 m, implying that the specific rate at which Th attaches to particles relative to that at which it is released from particles is higher in the upper ocean than in the deep ocean. In contrast, K/P increases with depth below 500 m. The parameters K and K/P display significant positive and negative monotonic relationship with P, respectively, which is collectively consistent with a particle concentration effect.
Decreased influence of Antarctic intermediate water in the tropical Atlantic during North Atlantic cold events

(Elsevier, 2014-01-15) Huang, Kuo-Fang ; Oppo, Delia W. ; Curry, William B.

Antarctic Intermediate Water (AAIW) is a key player in the global ocean circulation, contributing to the upper limb of the Atlantic Meridional Overturning Circulation (AMOC), and influencing interhemispheric heat exchange and the distribution of salinity, nutrients and carbon. However, the deglacial history of AAIW flow into the North Atlantic is controversial. Here we present a multicore-top neodymium isotope calibration, which confirms the ability of unclean foraminifera to faithfully record bottom water neodymium isotopic composition (εNdεNd) values in their authigenic coatings. We then present the first foraminifera-based reconstruction of εNdεNd from three sediment cores retrieved from within modern AAIW, in the western tropical North Atlantic. Our records reveal similar glacial and interglacial contributions of AAIW, and a pronounced decrease in the AAIW fraction during North Atlantic deglacial cold episodes, Heinrich Stadial 1 (HS1) and Younger Dryas (YD). Our results suggest two separate phases of reduced fraction of AAIW in the tropical Atlantic during HS1, with a greater reduction during early HS1. If a reduction in AAIW fraction also reflects reduced AMOC strength, this finding may explain why, in many regions, there are two phases of hydrologic change within HS1, and why atmospheric CO2 rose more rapidly during early than late HS1. Our result suggesting less flow of AAIW into the Atlantic during North Atlantic cold events contrasts with evidence from the Pacific, where intermediate-depth εNdεNd records may indicate increased flow of AAIW into the Pacific during the these same events. Antiphased εNdεNd behavior between intermediate depths of the North Atlantic and Pacific implies that the flow of AAIW into Atlantic and Pacific seesawed during the last deglaciation.
Th-230 and Pa-231 on GEOTRACES GA03, the US GEOTRACES North Atlantic transect, and implications for modern and paleoceanographic chemical fluxes

( 2014-07) Hayes, Christopher T. ; Anderson, Robert F. ; Fleisher, Martin Q. ; Huang, Kuo-Fang ; Robinson, Laura F. ; Lu, Yanbin ; Cheng, Hai ; Edwards, R. Lawrence ; Moran, S. Bradley

The long-lived uranium decay products 230Th and 231Pa are widely used as quantitative tracers of adsorption to sinking particles (scavenging) in the ocean by exploiting the principles of radioactive disequilibria. Because of their preservation in the Pleistocene sediment record and through largely untested assumptions about their chemical behavior in the water column, the two radionuclides have also been used as proxies for a variety of chemical fluxes in the past ocean. This includes the vertical flux of particulate matter to the seafloor, the lateral flux of insoluble elements to continental margins (boundary scavenging), and the southward flux of water out of the deep North Atlantic. In a section of unprecedented vertical and zonal resolution, the distributions of 230Th and 231Pa across the North Atlantic shed light on the marine cycling of these radionuclides and further inform their use as tracers of chemical flux. Enhanced scavenging intensities are observed in benthic layers of resuspended sediments on the eastern and western margins and in a hydrothermal plume emanating from the Mid-Atlantic Ridge. Boundary scavenging is clearly expressed in the water column along a transect between Mauritania and Cape Verde which is used to quantify a bias in sediment fluxes calculated using 230Th-normalization and to demonstrate enhanced 231Pa removal from the deep North Atlantic by this mechanism. The influence of deep ocean ventilation that leads to the southward export of 231Pa is apparent. The 231Pa/230Th ratio, however, predominantly reflects spatial variability in scavenging intensity, complicating its applicability as a proxy for the Atlantic meridional overturning circulation.
Intensity of Th and Pa scavenging partitioned by particle chemistry in the North Atlantic Ocean

( 2015-01) Hayes, Christopher T. ; Anderson, Robert F. ; Fleisher, Martin Q. ; Vivancos, Sebastian M. ; Lam, Phoebe J. ; Ohnemus, Daniel C. ; Huang, Kuo-Fang ; Robinson, Laura F. ; Lu, Yanbin ; Cheng, Hai ; Edwards, R. Lawrence ; Moran, S. Bradley

The natural radionuclides 231Pa and 230Th are incorporated into the marine sediment record by scavenging, or adsorption to various particle types, via chemical reactions that are not fully understood. Because these isotopes have potential value in tracing several oceanographic processes, we investigate the nature of scavenging using trans-Atlantic measurements of dissolved (<0.45 μm) and particulate (0.8-51 μm) 231Pa and 230Th, together with major particle composition. We find widespread impact of intense scavenging by authigenic Fe/Mn (hydr)oxides, in the form of hydrothermal particles emanating from the Mid-Atlantic ridge and particles resuspended from reducing conditions near the seafloor off the coast of West Africa. Biogenic opal was not found to be a significant scavenging phase for either element in this sample set, essentially because of its low abundance and small dynamic range at the studied sites. Distribution coefficients in shallow (< 200 m) depths are anomalously low which suggests either the unexpected result of a low scavenging intensity for organic matter or that, in water masses containing abundant organic-rich particles, a greater percentage of radionuclides exist in the colloidal or complexed phase. In addition to particle concentration, the oceanic distribution of particle types likely plays a significant role in the ultimate distribution of sedimentary 230Th and 231Pa.
Nonhomogeneous seawater Sr isotopic composition in the coastal oceans : a novel tool for tracing water masses and submarine groundwater discharge

(American Geophysical Union, 2011-05-07) Huang, Kuo-Fang ; You, Chen-Feng ; Chung, Chuan-Hsiung ; Lin, In-Tian

Here we present high-precision (2σ = ±3 ppm) 87Sr/86Sr measurements in coastal waters, together with salinity, to evaluate water mass mixing and the influence of submarine groundwater discharge (SGD) in coastal waters and marginal seas. Nonhomogeneous Sr isotopic variations in water columns were documented in the Southern Okinawa Trough (SOT), South China Sea, and Kao-ping Canyon (KPC), where seawater 87Sr/86Sr varied up to 70 ppm. Seawater Sr isotopic composition changes only slightly in the upper 200 m of the SOT but was detectable and highly correlated with salinity, indicating a mixing between radiogenic North Pacific Tropical Water (high 87Sr/86Sr and high salinity) at 100–150 m and a less radiogenic component with low 87Sr/86Sr and low salinity at ∼200 m. Vertical profiles of seawater 87Sr/86Sr along the KPC show significant variations, suggesting dynamic mixing affected by continental inputs (i.e., river runoff and SGD) in this region. These results highlight the potential use of seawater Sr isotopes as a powerful tracer for determining mixing ratios and the dynamic mixing of oceanic water masses, especially in coastal and marginal seas.
Atlantic circulation and ice sheet influences on upper South Atlantic temperatures during the last deglaciation

(American Geophysical Union, 2019-05-28) Umling, Natalie E. ; Oppo, Delia W. ; Chen, P. ; Yu, Jimin ; Liu, Zhengyu ; Yan, Mi ; Gebbie, Geoffrey A. ; Lund, David C. ; Pietro, Kathryn R. ; Jin, Z. D. ; Huang, Kuo-Fang ; Costa, Karen ; Toledo, Felipe Antonio de Lima

Atlantic Meridional Overturning Circulation (AMOC) disruption during the last deglaciation is hypothesized to have caused large subsurface ocean temperature anomalies, but records from key regions are not available to test this hypothesis, and other possible drivers of warming have not been fully considered. Here, we present the first reliable evidence for subsurface warming in the South Atlantic during Heinrich Stadial 1, confirming the link between large‐scale heat redistribution and AMOC. Warming extends across the Bølling‐Allerød despite predicted cooling at this time, thus spanning intervals of both weak and strong AMOC indicating another forcing mechanism that may have been previously overlooked. Transient model simulations and quasi‐conservative water mass tracers suggest that reduced northward upper ocean heat transport was responsible for the early deglacial (Heinrich Stadial 1) accumulation of heat at our shallower (~1,100 m) site. In contrast, the results suggest that warming at our deeper site (~1,900 m) site was dominated by southward advection of North Atlantic middepth heat anomalies. During the Bølling‐Allerød, the demise of ice sheets resulted in oceanographic changes in the North Atlantic that reduced convective heat loss to the atmosphere, causing subsurface warming that overwhelmed the cooling expected from an AMOC reinvigoration. The data and simulations suggest that rising atmospheric CO2 did not contribute significantly to deglacial subsurface warming at our sites.
The GEOTRACES Intermediate Data Product 2014

(Elsevier, 2015-04-16) Mawji, Edward ; Schlitzer, Reiner ; Dodas, Elena Masferrer ; Abadie, Cyril ; Abouchami, Wafa ; Anderson, Robert F. ; Baars, Oliver ; Bakker, Karel ; Baskaran, Mark ; Bates, Nicholas R. ; Bluhm, Katrin ; Bowie, Andrew R. ; Bown, Johann ; Boye, Marie ; Marie, Edward A. ; Branellec, Pierre ; Bruland, Kenneth W. ; Brzezinski, Mark A. ; Bucciarelli, Eva ; Buesseler, Ken O. ; Butler, Edward ; Cai, Pinghe ; Cardinal, Damien ; Casciotti, Karen L. ; Chaves, Joaquin E. ; Cheng, Hai ; Chever, Fanny ; Church, Thomas M. ; Colman, Albert S. ; Conway, Tim M. ; Croot, Peter L. ; Cutter, Gregory A. ; Baar, Hein J. W. de ; de Souza, Gregory F. ; Dehairs, Frank ; Deng, Feifei ; Dieu, Huong Thi ; Dulaquais, Gabriel ; Echegoyen-Sanz, Yolanda ; Edwards, R. Lawrence ; Fahrbach, Eberhard ; Fitzsimmons, Jessica N. ; Fleisher, Martin Q. ; Frank, Martin ; Friedrich, Jana ; Fripiat, Francois ; Galer, Stephen J. G. ; Gamo, Toshitaka ; Garcia Solsona, Ester ; Gerringa, Loes J. A. ; Godoy, Jose Marcus ; Gonzalez, Santiago ; Grossteffan, Emilie ; Hatta, Mariko ; Hayes, Christopher T. ; Heller, Maija Iris ; Henderson, Gideon M. ; Huang, Kuo-Fang ; Jeandel, Catherine ; Jenkins, William J. ; John, Seth G. ; Kenna, Timothy C. ; Klunder, Maarten ; Kretschmer, Sven ; Kumamoto, Yuichiro ; Laan, Patrick ; Labatut, Marie ; Lacan, Francois ; Lam, Phoebe J. ; Lannuzel, Delphine ; le Moigne, Frederique ; Lechtenfeld, Oliver J. ; Lohan, Maeve C. ; Lu, Yanbin ; Masqué, Pere ; McClain, Charles R. ; Measures, Christopher I. ; Middag, Rob ; Moffett, James W. ; Navidad, Alicia ; Nishioka, Jun ; Noble, Abigail E. ; Obata, Hajime ; Ohnemus, Daniel C. ; Owens, Stephanie A. ; Planchon, Frederic ; Pradoux, Catherine ; Puigcorbe, Viena ; Quay, Paul D. ; Radic, Amandine ; Rehkamper, Mark ; Remenyi, Tomas A. ; Rijkenberg, Micha J. A. ; Rintoul, Stephen R. ; Robinson, Laura F. ; Roeske, Tobias ; Rosenberg, Mark ; Rutgers van der Loeff, Michiel M. ; Ryabenko, Evgenia ; Saito, Mak A. ; Roshan, Saeed ; Salt, Lesley ; Sarthou, Geraldine ; Schauer, Ursula ; Scott, Peter M. ; Sedwick, Peter N. ; Sha, Lijuan ; Shiller, Alan M. ; Sigman, Daniel M. ; Smethie, William M. ; Smith, Geoffrey J. ; Sohrin, Yoshiki ; Speich, Sabrina ; Stichel, Torben ; Stutsman, Johnny ; Swift, James H. ; Tagliabue, Alessandro ; Thomas, Alexander L. ; Tsunogai, Urumu ; Twining, Benjamin S. ; van Aken, Hendrik M. ; van Heuven, Steven ; van Ooijen, Jan ; van Weerlee, Evaline ; Venchiarutti, Celia ; Voelker, Antje H. L. ; Wake, Bronwyn ; Warner, Mark J. ; Woodward, E. Malcolm S. ; Wu, Jingfeng ; Wyatt, Neil ; Yoshikawa, Hisayuki ; Zheng, Xin-Yuan ; Xue, Zichen ; Zieringer, Moritz ; Zimmer, Louise A.

The GEOTRACES Intermediate Data Product 2014 (IDP2014) is the first publicly available data product of the international GEOTRACES programme, and contains data measured and quality controlled before the end of 2013. It consists of two parts: (1) a compilation of digital data for more than 200 trace elements and isotopes (TEIs) as well as classical hydrographic parameters, and (2) the eGEOTRACES Electronic Atlas providing a strongly inter-linked on-line atlas including more than 300 section plots and 90 animated 3D scenes. The IDP2014 covers the Atlantic, Arctic, and Indian oceans, exhibiting highest data density in the Atlantic. The TEI data in the IDP2014 are quality controlled by careful assessment of intercalibration results and multi-laboratory data comparisons at cross-over stations. The digital data are provided in several formats, including ASCII spreadsheet, Excel spreadsheet, netCDF, and Ocean Data View collection. In addition to the actual data values the IDP2014 also contains data quality flags and 1-σ data error values where available. Quality flags and error values are useful for data filtering. Metadata about data originators, analytical methods and original publications related to the data are linked to the data in an easily accessible way. The eGEOTRACES Electronic Atlas is the visual representation of the IDP2014 data providing section plots and a new kind of animated 3D scenes. The basin-wide 3D scenes allow for viewing of data from many cruises at the same time, thereby providing quick overviews of large-scale tracer distributions. In addition, the 3D scenes provide geographical and bathymetric context that is crucial for the interpretation and assessment of observed tracer plumes, as well as for making inferences about controlling processes.
Data constraints on glacial Atlantic Water mass geometry and properties

(John Wiley & Sons, 2018-09-27) Oppo, Delia W. ; Gebbie, Geoffrey A. ; Huang, Kuo-Fang ; Curry, William B. ; Marchitto, Thomas M. ; Pietro, Kathryn R.

The chemical composition of benthic foraminifera from marine sediment cores provides information on how glacial subsurface water properties differed from modern, but separating the influence of changes in the origin and end‐member properties of subsurface water from changes in flows and mixing is challenging. Spatial gaps in coverage of glacial data add to the uncertainty. Here we present new data from cores collected from the Demerara Rise in the western tropical North Atlantic, including cores from the modern tropical phosphate maximum at Antarctic Intermediate Water (AAIW) depths. The results suggest lower phosphate concentration and higher carbonate saturation state within the phosphate maximum than modern despite similar carbon isotope values, consistent with less accumulation of respired nutrients and carbon, and reduced air‐sea gas exchange in source waters to the region. An inversion of new and published glacial data confirms these inferences and further suggests that lower preformed nutrients in AAIW, and partial replacement of this still relatively high‐nutrient AAIW with nutrient‐depleted, carbonate‐rich waters sourced from the region of the modern‐day northern subtropics, also contributed to the observed changes. The results suggest that glacial preformed and remineralized phosphate were lower throughout the upper Atlantic, but deep phosphate concentration was higher. The inversion, which relies on the fidelity of the paleoceanographic data, suggests that the partial replacement of North Atlantic sourced deep water by Southern Ocean Water was largely responsible for the apparent deep North Atlantic phosphate increase, rather than greater remineralization.
Antarctic intermediate water circulation in the South Atlantic over the past 25,000 years

(John Wiley & Sons, 2016-10-05) Howe, Jacob N. W. ; Piotrowski, Alexander M. ; Oppo, Delia W. ; Huang, Kuo-Fang ; Mulitza, Stefan ; Chiessi, Cristiano M. ; Blusztajn, Jerzy S.

Antarctic Intermediate Water is an essential limb of the Atlantic meridional overturning circulation that redistributes heat and nutrients within the Atlantic Ocean. Existing reconstructions have yielded conflicting results on the history of Antarctic Intermediate Water penetration into the Atlantic across the most recent glacial termination. In this study we present leachate, foraminiferal, and detrital neodymium isotope data from three intermediate-depth cores collected from the southern Brazil margin in the South Atlantic covering the past 25 kyr. These results reveal that strong chemical leaching following decarbonation does not extract past seawater neodymium composition in this location. The new foraminiferal records reveal no changes in seawater Nd isotopes during abrupt Northern Hemisphere cold events at these sites. We therefore conclude that there is no evidence for greater incursion of Antarctic Intermediate Water into the South Atlantic during either the Younger Dryas or Heinrich Stadial 1. We do, however, observe more radiogenic Nd isotope values in the intermediate-depth South Atlantic during the mid-Holocene. This radiogenic excursion coincides with evidence for a southward shift in the Southern Hemisphere westerlies that may have resulted in a greater entrainment of radiogenic Pacific-sourced water during intermediate water production in the Atlantic sector of the Southern Ocean. Our intermediate-depth records show similar values to a deglacial foraminiferal Nd isotope record from the deep South Atlantic during the Younger Dryas but are clearly distinct during the Last Glacial Maximum and Heinrich Stadial 1, demonstrating that the South Atlantic remained chemically stratified during Heinrich Stadial 1.
Glacial-interglacial Nd isotope variability of North Atlantic Deep Water modulated by North American ice sheet

(Nature Research, 2019-12-18) Zhao, Ning ; Oppo, Delia W. ; Huang, Kuo-Fang ; Howe, Jacob N. W. ; Blusztajn, Jerzy S. ; Keigwin, Lloyd D.

The Nd isotope composition of seawater has been used to reconstruct past changes in the contribution of different water masses to the deep ocean. In the absence of contrary information, the Nd isotope compositions of endmember water masses are usually assumed constant during the Quaternary. Here we show that the Nd isotope composition of North Atlantic Deep Water (NADW), a major component of the global overturning ocean circulation, was significantly more radiogenic than modern during the Last Glacial Maximum (LGM), and shifted towards modern values during the deglaciation. We propose that weathering contributions of unradiogenic Nd modulated by the North American Ice Sheet dominated the evolution of the NADW Nd isotope endmember. If water mass mixing dominated the distribution of deep glacial Atlantic Nd isotopes, our results would imply a larger fraction of NADW in the deep Atlantic during the LGM and deglaciation than reconstructed with a constant northern endmember.
Deglacial temperature and carbonate saturation state variability in the tropical Atlantic at Antarctic Intermediate Water Depths

(Wiley, 2023-08-26) Oppo, Delia W. ; Lu, Wanyi ; Huang, Kuo-Fang ; Umling, Natalie E. ; Guo, Weifu ; Yu, Jimin ; Curry, William B. ; Marchitto, Thomas M. ; Wang, Shouyi

The Atlantic Meridional Overturning Circulation (AMOC) is characterized by northward flow in the upper ocean and southward flow in the deep ocean. Understanding how the AMOC has changed in the past, and how such changes have affected surface climate and the distribution of ocean heat, carbon, and nutrients is important but challenging, as reconstructions of subsurface ocean properties are sometimes ambiguous. Here, we use the chemical composition of seafloor shells from a site in the western tropical Atlantic Ocean at ∼950 m water depth, within the northward-flowing limb of the AMOC, to reconstruct temperature, nutrients, and carbon content during the end of the last Ice Age, an interval when AMOC strength is believed to have varied. Our results support a link between AMOC strength and tropical Atlantic nutrient content, and further suggest that both rising atmospheric CO2 and AMOC variations influenced temperatures and carbon in the subsurface tropical Atlantic Ocean.
The GEOTRACES Intermediate Data Product 2017

(Elsevier, 2018-06-01) Schlitzer, Reiner ; Anderson, Robert F. ; Dodas, Elena Masferrer ; Lohan, Maeve C. ; Geibert, Walter ; Tagliabue, Alessandro ; Bowie, Andrew R. ; Jeandel, Catherine ; Maldonado, Maria T. ; Landing, William M. ; Cockwell, Donna ; Abadie, Cyril ; Abouchami, Wafa ; Achterberg, Eric P. ; Agather, Alison ; Aguliar-Islas, Ana ; van Aken, Hendrik M. ; Andersen, Morten ; Archer, Corey ; Auro, Maureen E. ; Baar, Hein J. W. de ; Baars, Oliver ; Baker, Alex R. ; Bakker, Karel ; Basak, Chandranath ; Baskaran, Mark ; Bates, Nicholas R. ; Bauch, Dorothea ; van Beek, Pieter ; Behrens, Melanie K. ; Black, Erin E. ; Bluhm, Katrin ; Bopp, Laurent ; Bouman, Heather ; Bowman, Katlin ; Bown, Johann ; Boyd, Philip ; Boye, Marie ; Boyle, Edward A. ; Branellec, Pierre ; Bridgestock, Luke ; Brissebrat, Guillaume ; Browning, Thomas A. ; Bruland, Kenneth W. ; Brumsack, Hans-Jürgen ; Brzezinski, Mark A. ; Buck, Clifton S. ; Buck, Kristen N. ; Buesseler, Ken O. ; Bull, Abby ; Butler, Edward ; Cai, Pinghe ; Cámara Mor, Patricia ; Cardinal, Damien ; Carlson, Craig ; Carrasco, Gonzalo ; Casacuberta, Nuria ; Casciotti, Karen L. ; Castrillejo, Maxi ; Chamizo, Elena ; Chance, Rosie ; Charette, Matthew A. ; Chaves, Joaquin E. ; Cheng, Hai ; Chever, Fanny ; Christl, Marcus ; Church, Thomas M. ; Closset, Ivia ; Colman, Albert S. ; Conway, Tim M. ; Cossa, Daniel ; Croot, Peter L. ; Cullen, Jay T. ; Cutter, Gregory A. ; Daniels, Chris ; Dehairs, Frank ; Deng, Feifei ; Dieu, Huong Thi ; Duggan, Brian ; Dulaquais, Gabriel ; Dumousseaud, Cynthia ; Echegoyen-Sanz, Yolanda ; Edwards, R. Lawrence ; Ellwood, Michael J. ; Fahrbach, Eberhard ; Fitzsimmons, Jessica N. ; Flegal, A. Russell ; Fleisher, Martin Q. ; van de Flierdt, Tina ; Frank, Martin ; Friedrich, Jana ; Fripiat, Francois ; Fröllje, Henning ; Galer, Stephen J. G. ; Gamo, Toshitaka ; Ganeshram, Raja S. ; Garcia-Orellana, Jordi ; Garcia Solsona, Ester ; Gault-Ringold, Melanie ; George, Ejin ; Gerringa, Loes J. A. ; Gilbert, Melissa ; Godoy, Jose Marcus ; Goldstein, Steven L. ; Gonzalez, Santiago ; Grissom, Karen ; Hammerschmidt, Chad R. ; Hartman, Alison ; Hassler, Christel ; Hathorne, Ed C. ; Hatta, Mariko ; Hawco, Nicholas J. ; Hayes, Christopher T. ; Heimbürger, Lars-Eric ; Helgoe, Josh ; Heller, Maija Iris ; Henderson, Gideon M. ; Henderson, Paul B. ; van Heuven, Steven ; Ho, Peng ; Horner, Tristan J. ; Hsieh, Yu-Te ; Huang, Kuo-Fang ; Humphreys, Matthew P. ; Isshiki, Kenji ; Jacquot, Jeremy E. ; Janssen, David J. ; Jenkins, William J. ; John, Seth ; Jones, Elizabeth M. ; Jones, Janice L. ; Kadko, David ; Kayser, Rick ; Kenna, Timothy C. ; Khondoker, Roulin ; Kim, Taejin ; Kipp, Lauren ; Klar, Jessica K. ; Klunder, Maarten ; Kretschmer, Sven ; Kumamoto, Yuichiro ; Laan, Patrick ; Labatut, Marie ; Lacan, Francois ; Lam, Phoebe J. ; Lambelet, Myriam ; Lamborg, Carl H. ; le Moigne, Frederique ; Le Roy, Emilie ; Lechtenfeld, Oliver J. ; Lee, Jong-Mi ; Lherminier, Pascale ; Little, Susan ; López-Lora, Mercedes ; Lu, Yanbin ; Masque, Pere ; Mawji, Edward ; McClain, Charles R. ; Measures, Christopher I. ; Mehic, Sanjin ; Menzel Barraqueta, Jan-Lukas ; Merwe, Pier van der ; Middag, Rob ; Mieruch, Sebastian ; Milne, Angela ; Minami, Tomoharu ; Moffett, James W. ; Moncoiffe, Gwenaelle ; Moore, Willard S. ; Morris, Paul J. ; Morton, Peter L. ; Nakaguchi, Yuzuru ; Nakayama, Noriko ; Niedermiller, John ; Nishioka, Jun ; Nishiuchi, Akira ; Noble, Abigail E. ; Obata, Hajime ; Ober, Sven ; Ohnemus, Daniel C. ; van Ooijen, Jan ; O'Sullivan, Jeanette ; Owens, Stephanie A. ; Pahnke, Katharina ; Paul, Maxence ; Pavia, Frank ; Pena, Leopoldo D. ; Peters, Brian ; Planchon, Frederic ; Planquette, Helene ; Pradoux, Catherine ; Puigcorbé, Viena ; Quay, Paul D. ; Queroue, Fabien ; Radic, Amandine ; Rauschenberg, Sara ; Rehkämper, Mark ; Rember, Robert ; Remenyi, Tomas A. ; Resing, Joseph A. ; Rickli, Joerg ; Rigaud, Sylvain ; Rijkenberg, Micha J. A. ; Rintoul, Stephen R. ; Robinson, Laura F. ; Roca-Martí, Montserrat ; Rodellas, Valenti ; Roeske, Tobias ; Rolison, John M. ; Rosenberg, Mark ; Roshan, Saeed ; Rutgers van der Loeff, Michiel M. ; Ryabenko, Evgenia ; Saito, Mak A. ; Salt, Lesley ; Sanial, Virginie ; Sarthou, Geraldine ; Schallenberg, Christina ; Schauer, Ursula ; Scher, Howie ; Schlosser, Christian ; Schnetger, Bernhard ; Scott, Peter M. ; Sedwick, Peter N. ; Semiletov, Igor P. ; Shelley, Rachel U. ; Sherrell, Robert M. ; Shiller, Alan M. ; Sigman, Daniel M. ; Singh, Sunil Kumar ; Slagter, Hans ; Slater, Emma ; Smethie, William M. ; Snaith, Helen ; Sohrin, Yoshiki ; Sohst, Bettina M. ; Sonke, Jeroen E. ; Speich, Sabrina ; Steinfeldt, Reiner ; Stewart, Gillian ; Stichel, Torben ; Stirling, Claudine H. ; Stutsman, Johnny ; Swarr, Gretchen J. ; Swift, James H. ; Thomas, Alexander ; Thorne, Kay ; Till, Claire P. ; Till, Ralph ; Townsend, Ashley T. ; Townsend, Emily ; Tuerena, Robyn ; Twining, Benjamin S. ; Vance, Derek ; Velazquez, Sue ; Venchiarutti, Celia ; Villa-Alfageme, Maria ; Vivancos, Sebastian M. ; Voelker, Antje H. L. ; Wake, Bronwyn ; Warner, Mark J. ; Watson, Ros ; van Weerlee, Evaline ; Weigand, M. Alexandra ; Weinstein, Yishai ; Weiss, Dominik ; Wisotzki, Andreas ; Woodward, E. Malcolm S. ; Wu, Jingfeng ; Wu, Yingzhe ; Wuttig, Kathrin ; Wyatt, Neil ; Xiang, Yang ; Xie, Ruifang C. ; Xue, Zichen ; Yoshikawa, Hisayuki ; Zhang, Jing ; Zhang, Pu ; Zhao, Ye ; Zheng, Linjie ; Zheng, Xin-Yuan ; Zieringer, Moritz ; Zimmer, Louise A. ; Ziveri, Patrizia ; Zunino, Patricia ; Zurbrick, Cheryl

The GEOTRACES Intermediate Data Product 2017 (IDP2017) is the second publicly available data product of the international GEOTRACES programme, and contains data measured and quality controlled before the end of 2016. The IDP2017 includes data from the Atlantic, Pacific, Arctic, Southern and Indian oceans, with about twice the data volume of the previous IDP2014. For the first time, the IDP2017 contains data for a large suite of biogeochemical parameters as well as aerosol and rain data characterising atmospheric trace element and isotope (TEI) sources. The TEI data in the IDP2017 are quality controlled by careful assessment of intercalibration results and multi-laboratory data comparisons at crossover stations. The IDP2017 consists of two parts: (1) a compilation of digital data for more than 450 TEIs as well as standard hydrographic parameters, and (2) the eGEOTRACES Electronic Atlas providing an on-line atlas that includes more than 590 section plots and 130 animated 3D scenes. The digital data are provided in several formats, including ASCII, Excel spreadsheet, netCDF, and Ocean Data View collection. Users can download the full data packages or make their own custom selections with a new on-line data extraction service. In addition to the actual data values, the IDP2017 also contains data quality flags and 1-σ data error values where available. Quality flags and error values are useful for data filtering and for statistical analysis. Metadata about data originators, analytical methods and original publications related to the data are linked in an easily accessible way. The eGEOTRACES Electronic Atlas is the visual representation of the IDP2017 as section plots and rotating 3D scenes. The basin-wide 3D scenes combine data from many cruises and provide quick overviews of large-scale tracer distributions. These 3D scenes provide geographical and bathymetric context that is crucial for the interpretation and assessment of tracer plumes near ocean margins or along ridges. The IDP2017 is the result of a truly international effort involving 326 researchers from 25 countries. This publication provides the critical reference for unpublished data, as well as for studies that make use of a large cross-section of data from the IDP2017. This article is part of a special issue entitled: Conway GEOTRACES - edited by Tim M. Conway, Tristan Horner, Yves Plancherel, and Aridane G. González.

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