Morris
Paul J.
Morris
Paul J.
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ArticleIntercalibration studies of short-lived thorium-234 in the water column and marine particles(Association for the Sciences of Limnology and Oceanography, 2012-09) Maiti, Kanchan ; Buesseler, Ken O. ; Pike, Steven M. ; Benitez-Nelson, Claudia R. ; Cai, Pinghe ; Chen, Weifang ; Cochran, Kirk ; Dai, Minhan ; Dehairs, Frank ; Gasser, Beat ; Kelly, Roger P. ; Masqué, Pere ; Miller, Lisa A. ; Miquel, Juan Carlos ; Moran, S. Bradley ; Morris, Paul J. ; Peine, Florian ; Planchon, Frederic ; Renfro, Alisha A. ; Rutgers van der Loeff, Michiel M. ; Santschi, Peter H. ; Turnewitsch, Robert ; Waples, James T. ; Xu, ChenIntercomparision of 234Th measurements in both water and particulate samples was carried out between 15 laboratories worldwide, as a part of GEOTRACES inter-calibration program. Particulate samples from four different stations namely BATS (both shallow and deep) and shelf station (shallow) in Atlantic and SAFE (both shallow and deep) and Santa Barbara station (shallow) in Pacific were used in the effort. Particulate intercalibration results indicate good agreement between all the participating labs with data from all labs falling within the 95% confidence interval around the mean for most instances. Filter type experiments indicate no significant differences in 234Th activities between filter types and pore sizes (0.2-0.8 μm). The only exception are the quartz filters, which are associated with 10% to 20% higher 234Th activities attributed to sorption of dissolved 234Th. Flow rate experiments showed a trend of decreasing 234Th activities with increasing flow rates (2-9 L min-1) for > 51 μm size particles, indicating particle loss during the pumping process. No change in 234Th activities on small particles was observed with increasing flow-rates. 234Th intercalibration results from deep water samples at SAFe station indicate a variability of < 3% amongst labs while dissolved 234Th data from surface water at Santa Barbara Station show a less robust agreement, possibly due to the loss of 234Th from decay and large in-growth corrections as a result of long gap between sample collection and processing.
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PreprintRadium isotopes as tracers of iron sources fueling a Southern Ocean phytoplankton bloom( 2007-04-24) Charette, Matthew A. ; Gonneea, Meagan E. ; Morris, Paul J. ; Statham, Peter J. ; Fones, Gary R. ; Planquette, Helene ; Salter, Ian ; Naveira Garabato, Alberto C.Elevated levels of productivity in the wake of Southern Ocean island systems are common despite the fact that they are encircled by high nutrient low chlorophyll (HNLC) waters. In the Crozet Plateau region, it has been hypothesized that iron from island runoff or sediments of the plateau could be fueling the austral summer phytoplankton bloom. Here, we use radium isotopes to quantify the rates of surface ocean iron supply fueling the bloom in the Crozet Plateau region. A 1-D eddy-diffusion-mixing model applied to a 228Ra profile (t1/2 = 5.75 yr) at a station north of the islands suggested fast vertical mixing in the upper 300 m (Kz = 11-100 cm2 s- 1) with slower mixing between 300 and 1000 m (Kz = 1.5 cm2 s-1). This estimate is discussed in the context of Kz derived from the CTD/LADCP data. In combination with the dissolved Fe profile at this location, we estimated a vertical flux of between 5.6 and 31 nmol Fe m-2 d-1. The cross-plateau gradients in the short-lived radium isotopes, 224Ra (t1/2 = 3.66 d) and 223Ra (t1/2 = 11.4 d), yielded horizontal eddy diffusivities (Kh) of 39 m2 s-1 and 6.6 m2 s-1, respectively. If we assume that the islands (surface runoff) alone were supplying dissolved Fe to the bloom region, then the flux estimates range from 2.3 to 14 nmol Fe m-2 d-1. If the plateau sediments are considered a source of Fe, and conveyed to the bloom region through deep winter mixing combined with horizontal transport, then this flux may be as high as 64 to 390 nmol Fe m-2 d-1. Combined, these Fe sources are sufficient to initiate and maintain the annual phytoplankton bloom.
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PreprintA review of present techniques and methodological advances in analyzing Th-234 in aquatic systems( 2005-10-10) Rutgers van der Loeff, Michiel M. ; Sarin, Manmohan M. ; Baskaran, Mark ; Benitez-Nelson, Claudia R. ; Buesseler, Ken O. ; Charette, Matthew A. ; Dai, Minhan ; Gustafsson, Orjan ; Masqué, Pere ; Morris, Paul J. ; Orlandini, Kent ; Rodriguez y Baena, Alessia ; Savoye, Nicolas ; Schmidt, Sabine ; Turnewitsch, Robert ; Voge, Ingrid ; Waples, James T.The short-lived thorium isotope 234Th (half-life 24.1 days) has been used as a tracer for a variety of transport processes in aquatic systems. Its use as a tracer of oceanic export via sinking particles has stimulated a rapidly increasing number of studies that require analyses of 234Th in both marine and freshwater systems. The original 234Th method is labour intensive. Thus, there has been a quest for simpler techniques that require smaller sample volumes. Here, we review current methodologies in the collection and analysis of 234Th from the water column, discuss their individual strengths and weaknesses, and provide an outlook on possible further improvements and future challenges. Also included in this review are recommendations on calibration procedures and the production of standard reference materials as well as a flow chart designed to help researchers find the most appropriate 234Th analytical technique for a specific aquatic regime and known sampling constraints.
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PreprintNew perspectives on radium behavior within a subterranean estuary( 2007-04-02) Gonneea, Meagan E. ; Morris, Paul J. ; Dulaiova, Henrieta ; Charette, Matthew A.Over the past decade, radium isotopes have been frequently applied as tracers of submarine groundwater discharge (SGD). The unique radium signature of SGD is acquired within the subterranean estuary, a mixing zone between fresh groundwater and seawater in coastal aquifers, yet little is known about what controls Ra cycling in this system. The focus of this study was to examine controls on sediment and groundwater radium activities within permeable aquifer sands (Waquoit Bay, MA, USA) through a combination of field and laboratory studies. In the field, a series of sediment cores and corresponding groundwater profiles were collected for analysis of the four radium isotopes, as well as dissolved and sediment associated manganese, iron, and barium. We found that in addition to greater desorption at increasing salinity, radium was also closely tied to manganese and iron redox cycling within these sediments. A series of laboratory adsorption/desorption experiments helped elucidate the importance of 1) contact time between sediment and water, 2) salinity of water in contact with sediment, 3) redox conditions of water in contact with sediment, and 4) the chemical characteristics of sediment on radium adsorption/desorption. We found that these reactions are rapid (on the order of hours), desorption increases with increasing salinity and decreasing pH, and the presence of Fe and Mn (hydr)oxides on the sediment inhibit the release of radium. These sediments have a large capacity to sorb radium from fresh water. Combined with these experimental results, we present evidence from time series groundwater sampling that within this subterranean estuary there are cyclic periods of Ra accumulation and release controlled by changing salinity and redox conditions.
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ArticleDoes a ballast effect occur in the surface ocean?(American Geophysical Union, 2010-04-29) Sanders, Richard J. ; Morris, Paul J. ; Poulton, Alex J. ; Stinchcombe, Mark C. ; Charalampopoulou, Anastasia ; Lucas, Mike I. ; Thomalla, Sandy J.The oceanic biological carbon pump (BCP), a large (10 GT C yr−1) component of the global carbon cycle, is dominated by the sinking (export) of particulate organic carbon (POC) from surface waters. In the deep ocean, strong correlations between downward fluxes of biominerals and POC (the so-called ‘ballast effect’) suggest a potential causal relationship, the nature of which remains uncertain. We show that similar correlations occur in the upper ocean with high rates of export only occurring when biominerals are also exported. Exported particles are generally biomineral rich relative to the upper ocean standing stock, due either to: (1) exported material being formed from the aggregation of a biomineral rich subset of upper ocean particles; or (2) the unfractionated aggregation of the upper ocean particulate pool with respiration then selectively removing POC relative to biominerals until particles are dense enough to sink.
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ArticleA reduced estimate of the strength of the ocean's biological carbon pump(American Geophysical Union, 2011-02-18) Henson, Stephanie A. ; Sanders, Richard J. ; Madsen, Esben ; Morris, Paul J. ; Le Moigne, Frederic A. C. ; Quartly, Graham D.A major term in the global carbon cycle is the ocean's biological carbon pump which is dominated by sinking of small organic particles from the surface ocean to its interior. Several different approaches to estimating the magnitude of the pump have been used, yielding a large range of estimates. Here, we use an alternative methodology, a thorium isotope tracer, that provides direct estimates of particulate organic carbon export. A large database of thorium-derived export measurements was compiled and extrapolated to the global scale by correlation with satellite sea surface temperature fields. Our estimates of export efficiency are significantly lower than those derived from the f-ratio, and we estimate global integrated carbon export as ∼5 GtC yr−1, lower than most current estimates. The lack of consensus amongst different methodologies on the strength of the biological carbon pump emphasises that our knowledge of a major planetary carbon flux remains incomplete.
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ArticleOn the proportion of ballast versus non-ballast associated carbon export in the surface ocean(American Geophysical Union, 2012-08-11) Le Moigne, Frederic A. C. ; Sanders, Richard J. ; Villa-Alfageme, Maria ; Martin, Adrian P. ; Pabortsava, Katsiaryna ; Planquette, Helene ; Morris, Paul J. ; Thomalla, Sandy J.The role of biominerals in driving carbon export from the surface ocean is unclear. We compiled surface particulate organic carbon (POC), and mineral ballast export fluxes from 55 different locations in the Atlantic and Southern Oceans. Substantial surface POC export accompanied by negligible mineral export was recorded implying that association with mineral phases is not a precondition for organic export to occur. The proportion of non-mineral associated sinking POC ranged from 0 to 80% and was highest in areas previously shown to be dominated by diatoms. This is consistent with previous estimates showing that transfer efficiency in such regions is low. However we propose that, rather than the low transfer efficiency arising from diatom blooms being inherently characterized by poorly packaged aggregates which are efficiently exported but which disintegrate readily in mid water, it is due to such environments having very high levels of unballasted organic C export.
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ArticleA carbon budget for a naturally iron fertilized bloom in the Southern Ocean(American Geophysical Union, 2011-07-08) Morris, Paul J. ; Sanders, Richard J.Subantarctic islands in the high-nutrient, low-chlorophyll (HNLC) Southern Ocean are natural sources of iron and stimulate blooms in their proximity, such as the one observed close to the Crozet Islands (52°E, 46°S). During 2004/2005, particulate organic carbon (POC) export was measured using the 234Th technique in the Crozet bloom and compared with an HNLC control region. Initial results showed that iron release had no effect on daily POC export rates, thus any iron-driven enhancement in POC export was due to a longer export phase in the bloom region when compared to the control region. The duration of the export event was empirically estimated by closing the silicon budget, thus allowing seasonal POC export to be calculated by applying the export duration to the daily rates of POC export. This yields a seasonal estimate of POC export that is 3.6 times larger (range 1.9–7.1) in the iron-fertilized region than in the HNLC control region. These estimates of POC export were then compared to independent estimates of organic matter storage in the upper ocean, which are significant in both the HNLC and control regions. Overall, integrated POC export was significantly (approximately 50%) lower than estimated seasonal new production, the fraction of production that is supported by inputs of new nutrients. Finally, the sequestration efficiency, the numerical relationship between the supply of the limiting nutrient, iron, and the key ecosystem function of POC export at 100 m, is estimated to be 16,790 mol:mol.
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ArticleFukushima Daiichi–derived radionuclides in the ocean : transport, fate, and impacts(Annual Reviews, 2016-06-30) Buesseler, Ken O. ; Dai, Minhan ; Aoyama, Michio ; Benitez-Nelson, Claudia R. ; Charmasson, Sabine ; Higley, Kathryn ; Maderich, Vladimir ; Masqué, Pere ; Morris, Paul J. ; Oughton, Deborah ; Smith, John N.The events that followed the Tohoku earthquake and tsunami on March 11, 2011, included the loss of power and overheating at the Fukushima Daiichi nuclear power plants, which led to extensive releases of radioactive gases, volatiles, and liquids, particularly to the coastal ocean. The fate of these radionuclides depends in large part on their oceanic geochemistry, physical processes, and biological uptake. Whereas radioactivity on land can be resampled and its distribution mapped, releases to the marine environment are harder to characterize owing to variability in ocean currents and the general challenges of sampling at sea. Five years later, it is appropriate to review what happened in terms of the sources, transport, and fate of these radionuclides in the ocean. In addition to the oceanic behavior of these contaminants, this review considers the potential health effects and societal impacts.
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ArticleThe 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, CherylThe 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.