ORCID Profile
0000-0003-1396-0601
Current Organisations
National University of Ireland Galway
,
University of Otago
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Publisher: CSIRO Publishing
Date: 2005
DOI: 10.1071/MF05097
Abstract: There is compelling evidence to demonstrate that phytoplankton in major regions of the world’s oceans are limited by the availability of certain trace elements, notably iron. Cobalt concentrations in open-ocean waters generally range between 10 and 120 pmol L−1 but such levels were not thought to limit phytoplankton growth. Herein, we present data for total dissolved cobalt and cobalt-complexing ligands for two stations located south (station 200) and north (station 204) of the Antarctic Polar Front (APF) along 20°E in the South Atlantic sector of the Southern Ocean. Results indicate that there was little difference between total cobalt concentrations south and north of the APF, whereas ligand concentrations were significantly higher (15–20 pmol L−1) for the upper water column south of the APF. Productivity in these waters was low at the time of this study however, numbers of large eukaryotic algal species were higher south of the APF, while north of the APF small eukaryotic and prokaryotic species dominated. The higher ligand concentrations measured at the southern station are probably related to higher algal numbers at this site. Because ligand concentrations were higher, inorganic cobalt concentrations (Co′) south of the APF are extremely low, at femtomolar levels, whereas north of the APF calculated Co′ are much higher at picomolar levels where ligand concentrations were lower.
Publisher: American Association for the Advancement of Science (AAAS)
Date: 09-07-2021
Abstract: Changing atmospheric acidity alters the delivery of nutrients to the ocean and affects marine productivity and ecology.
Publisher: Copernicus GmbH
Date: 21-03-2011
Abstract: Abstract. The Maritime Aerosol Network (MAN) has been collecting data over the oceans since November 2006. Over 80 cruises were completed through early 2010 with deployments continuing. Measurement areas included various parts of the Atlantic Ocean, the Northern and Southern Pacific Ocean, the South Indian Ocean, the Southern Ocean, the Arctic Ocean and inland seas. MAN deploys Microtops hand-held sunphotometers and utilizes a calibration procedure and data processing traceable to AERONET. Data collection included areas that previously had no aerosol optical depth (AOD) coverage at all, particularly vast areas of the Southern Ocean. The MAN data archive provides a valuable resource for aerosol studies in maritime environments. In the current paper we present results of AOD measurements over the oceans, and make a comparison with satellite AOD retrievals and model simulations.
Publisher: American Chemical Society (ACS)
Date: 19-02-2019
Publisher: American Chemical Society (ACS)
Date: 22-08-2013
DOI: 10.1021/ES4016603
Abstract: Manganese (Mn) is a required element for oceanic phytoplankton as it plays a critical role in photosynthesis, through its unique redox chemistry, as the active site in photosystem II, and in enzymes that act as defenses against reactive oxygen species (ROS), most notably for protection against superoxide (O2(-)), through the action of superoxide dismutase (SOD), and against hydrogen peroxide (H2O2) via peroxidases and catalases. The distribution and redox speciation of Mn in the ocean is also apparently controlled by reactions with ROS. Here we examine the connections between ROS and dissolved Mn species in the upper ocean using field and laboratory experimental data. Our results suggest it is unlikely that significant concentrations of Mn(III) are produced in the euphotic zone, as in the absence of evidence for the existence of strong Mn(III) ligands, Mn(II) reacts with O2(-) to form the short-lived transient manganous superoxide, MnO2(+), which may react rapidly with other redox species in a manner similar to O2(-). Experiments with the strong Mn(III) chelator, desferrioxamine B (DFB), in seawater indicated that the Mn(III) species are unlikely to form, as formation of the precursor Mn(II) complex is hindered due to the stability of the Ca complex with DFB.
Publisher: Copernicus GmbH
Date: 18-04-2013
Abstract: Abstract. The deposition of atmospheric dust is the primary process supplying trace elements abundant in crustal rocks (e.g. Al, Mn and Fe) to the surface ocean. Upon deposition, the residence time in surface waters for each of these elements differs according to their chemical speciation and biological utilization. Presently, however, the chemical and physical processes occurring after atmospheric deposition are poorly constrained, principally because of the difficulty in following natural dust events in situ. In the present work we examined the temporal changes in the biogeochemistry of crustal metals (in particular Al, Mn and Fe) after an artificial dust deposition event. The experiment was contained inside trace metal clean mesocosms (0–12.5 m depths) deployed in the surface waters of the northwestern Mediterranean, close to the coast of Corsica within the frame of the DUNE project (a DUst experiment in a low Nutrient, low chlorophyll Ecosystem). Two consecutive artificial dust deposition events, each mimicking a wet deposition of 10 g m−2 of dust, were performed during the course of this DUNE-2 experiment. The changes in dissolved manganese (Mn), iron (Fe) and aluminum (Al) concentrations were followed immediately after the seeding with dust and over the following week. The Mn, Fe and Al inventories and loss or dissolution rates were determined. The evolution of the inventories after the two consecutive additions of dust showed distinct behaviors for dissolved Mn, Al and Fe. Even though the mixing conditions differed from one seeding to the other, Mn and Al showed clear increases directly after both seedings due to dissolution processes. Three days after the dust additions, Al concentrations decreased as a consequence of scavenging on sinking particles. Al appeared to be highly affected by the concentrations of biogenic particles, with an order of magnitude difference in its loss rates related to the increase of biomass after the addition of dust. In the case of dissolved Fe, it appears that the first dust addition resulted in a decrease as it was scavenged by sinking dust particles, whereas the second seeding induced dissolution of Fe from the dust particles due to the excess Fe binding ligand concentrations present at that time. This difference, which might be related to a change in Fe binding ligand concentration in the mesocosms, highlights the complex processes that control the solubility of Fe. Based on the inventories at the mesocosm scale, the estimations of the fractional solubility of metals from dust particles in seawater were 1.44 & m 0.19% and 0.91 ± 0.83% for Al and 41 ± 9% and 27 ± 19% for Mn for the first and the second dust addition. These values are in good agreement with laboratory-based estimates. For Fe no fractional solubility was obtained after the first seeding, but 0.12 ± 0.03% was estimated after the second seeding. Overall, the trace metal dataset presented here makes a significant contribution to enhancing our knowledge on the processes influencing trace metal release from Saharan dust and the subsequent processes of bio-uptake and scavenging in a low nutrient, low chlorophyll area.
Publisher: Springer Science and Business Media LLC
Date: 10-2000
DOI: 10.1038/35037500
Abstract: Changes in iron supply to oceanic plankton are thought to have a significant effect on concentrations of atmospheric carbon dioxide by altering rates of carbon sequestration, a theory known as the 'iron hypothesis'. For this reason, it is important to understand the response of pelagic biota to increased iron supply. Here we report the results of a mesoscale iron fertilization experiment in the polar Southern Ocean, where the potential to sequester iron-elevated algal carbon is probably greatest. Increased iron supply led to elevated phytoplankton biomass and rates of photosynthesis in surface waters, causing a large drawdown of carbon dioxide and macronutrients, and elevated dimethyl sulphide levels after 13 days. This drawdown was mostly due to the proliferation of diatom stocks. But downward export of biogenic carbon was not increased. Moreover, satellite observations of this massive bloom 30 days later, suggest that a sufficient proportion of the added iron was retained in surface waters. Our findings demonstrate that iron supply controls phytoplankton growth and community composition during summer in these polar Southern Ocean waters, but the fate of algal carbon remains unknown and depends on the interplay between the processes controlling export, remineralisation and timescales of water mass subduction.
Publisher: American Geophysical Union (AGU)
Date: 20-06-2007
DOI: 10.1029/2006JC003748
Publisher: American Chemical Society (ACS)
Date: 26-08-2013
DOI: 10.1021/ES401658T
Abstract: Superoxide (O2(-): IUPAC name dioxide (•1-)) is an important transient reactive oxygen species (ROS) in the ocean formed as an intermediate in the redox transformation of oxygen (O2) into hydrogen peroxide (H2O2) and vice versa. This highly reactive and very short-lived radical anion can be produced both via photochemical and biological processes in the ocean. In this paper we examine the decomposition rate of O2(-) throughout the water column, using new data collected in the Eastern Tropical North Atlantic (ETNA) Ocean. For this approach we applied a semi factorial experimental design to identify and quantify the pathways of the major identified sinks in the ocean. In this work we occupied six stations, two on the West African continental shelf and four open ocean stations, including the CVOO time series site adjacent to Cape Verde. Our results indicate that, in the surface ocean impacted by Saharan aerosols and coastal sediment resuspension, the main decay pathways for superoxide are via reactions with Mn(II) and organic matter.
Publisher: Elsevier BV
Date: 10-2021
Publisher: Elsevier BV
Date: 08-2015
Publisher: American Geophysical Union (AGU)
Date: 06-2010
DOI: 10.1029/2009GB003689
Publisher: American Geophysical Union (AGU)
Date: 12-2005
DOI: 10.1029/2005GB002494
Publisher: American Chemical Society (ACS)
Date: 22-10-2021
Publisher: Inter-Research Science Center
Date: 28-10-2010
DOI: 10.3354/AB00284
Publisher: Springer Science and Business Media LLC
Date: 26-11-2019
DOI: 10.1038/S41597-019-0288-Y
Abstract: The marine iodine cycle has significant impacts on air quality and atmospheric chemistry. Specifically, the reaction of iodide with ozone in the top few micrometres of the surface ocean is an important sink for tropospheric ozone (a pollutant gas) and the dominant source of reactive iodine to the atmosphere. Sea surface iodide parameterisations are now being implemented in air quality models, but these are currently a major source of uncertainty. Relatively little observational data is available to estimate the global surface iodide concentrations, and this data has not hitherto been openly available in a collated, digital form. Here we present all available sea surface ( m depth) iodide observations. The dataset includes values digitised from published manuscripts, published and unpublished data supplied directly by the originators, and data obtained from repositories. It contains 1342 data points, and spans latitudes from 70°S to 68°N, representing all major basins. The data may be used to model sea surface iodide concentrations or as a reference for future observations.
Publisher: American Geophysical Union (AGU)
Date: 09-2005
DOI: 10.1029/2004JC002601
Location: Brazil
Location: No location found
Location: United States of America
Location: United Kingdom of Great Britain and Northern Ireland
No related grants have been discovered for Peter Croot.