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  • 2020-2024  (14)
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  • 1
    Publication Date: 2023-02-24
    Description: This dataset contains measured labile particulate and total particulate trace element concentrations (Al, Ti, V, P, Fe, Mn, Co, Ni, Cu, and Cd) of water bottle samples collected during GEOTRACES expedition GN05 (PS100) between 21 July and 1 September 2016 on Northeast Greenland Shelf. Samples were collected using the ultra-clean CTD rosette, equipped with 24 × 12 L GoFlo bottles following GEOTRACES sampling protocols (Cutter et al., 2017; https://www.geotraces.org). Particulate TM samples were collected onto pre-acid leached Polyethersulfone (PES) Membrane filters (0.2 µm, Sartorius) with 1.2 - 4.1 L of seawater filtered per sample. Labile particulates were determined after applying a weak acid leach with a mild reducing agent and a short heating step with a total leach time of 2 h. Total particulates were then analyzed following a 15 h reflux digest at 150 °C using a mixture of hydrofluoric acid and nitric acid. The validation of labile and total particulate trace metal analyses was monitored by reference materials BCR-414 and PACS-3. Information on the analytical procedure including reference materials and limits of detection can be found in related published manuscripts. The concentrations reflect the mean and the corresponding uncertainty is calculated as the standard deviation to replicate measurements. Uncertainty is calculated as one standard deviation (1σ, STD) to replicate measurements via ICP-MS. Use of quality flags (QF) according to GEOTRACES policy (https://www.geotraces.org/geotraces-quality-flag-policy/).
    Keywords: Aluminium, particulate; Arctic; ARK-XXX/2, GN05; Bottle number; Cadmium, particulate; Cobalt, particulate; Copper, particulate; CTD/Rosette, ultra clean; CTD-UC; Date/Time of event; DEPTH, water; Event label; Flag; GEOTRACES; Global marine biogeochemical cycles of trace elements and their isotopes; Greenlandic Fjords; Iron, particulate; Labile particulate; LATITUDE; LONGITUDE; Manganese, particulate; Nickel, particulate; North Greenland Sea; particulate; Phosphorus, particulate; Polarstern; PS100; PS100/074-1; PS100/082-1; PS100/090-1; PS100/189-1; PS100/214-1; PS100/241-1; PS100/262-1; PS100/274-2; Standard deviation; Standard deviation, relative; Station label; Titanium, particulate; trace elements; trace metals; Vanadium, particulate
    Type: Dataset
    Format: text/tab-separated-values, 6594 data points
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  • 2
    Publication Date: 2024-01-04
    Description: This dataset contains measured isotopic compositions of noble gases (helium and neon) of water samples collected during the METEOR expedition (M176/2) between Sep 1st and Oct 6th, 2021 on the Rainbow hydrothermal field, Mid-Atlantic Ridge. Seawater samples for noble gases were collected in a copper pipe, which was connected to the Niskin bottles, with water flowing until bubbles in the tube were removed. While the water was flowing, the pipe was closed using an electrical drill and a ratchet to ensure it is tight enough. Helium and neon isotopes were analyzed at the University of Bremen, using the methods described by Sültenfuß et al. (2009). In detail, helium and neon were separated from other gases with a cryogenic system at 25 K. A fraction (3 %) of separated gases was diverted into the quadrupole mass spectrometer (QMS) (Balzers QMG112a®) to measure helium and neon. Upon raising the trap temperature to 45 K, helium and neon were released into the main sector field mass spectrometer (SMS) to measure the concentrations of 3He, 4He, and 20Ne. The measured concentrations were in a unit of CCSTP (cubic centimeters at standard temperature and pressure). delta3He (δ3He, in ‰) was calculated as: /[3He/4He(sample)/3He/4He(air)-1]× 100, and delta22Ne (δ22Ne, in ‰) was calculated as: [22Ne/20Ne(sample)/22Ne/20Ne(air)-1]*100. The background 3He (2.38 fM) in the deep ocean was calculated from the background δ3He (~ -1.7%) and equilibrium helium concentrations (~ 1.75 nM) at the salinity (35 PSU) and temperature (~ 3.5 °C) ranges of the seawater samples. The 3He concentrations contributed by atmospheric components were calculated by the [3He_A = 1.384 ×10**-6× 0.28823× (measured Ne - background Ne)]. The excess of 3He (3Hexs) was then calculated by extracting the measured 3He concentrations with the background 3He level, 3He_A, and 3He released from the decay of tritium (~ 0.1127 fmol/kg).
    Keywords: Bottle number; CTD/Rosette, ultra clean; CTD-UC; Depth, bathymetric; DEPTH, water; Event label; GEOTRACES; Global marine biogeochemical cycles of trace elements and their isotopes; GPF 21‐2_049, Rainbow Plume; Helium-3; Helium-3/Helium-4; Helium-3 excess; Helium-4; hydrothermal systems; LATITUDE; LONGITUDE; M176/2; M176/2_10-3; M176/2_12-1; M176/2_13-3; M176/2_14-3; M176/2_15-3; M176/2_16-1; M176/2_17-2; M176/2_18-2; M176/2_19-2; M176/2_21-2; M176/2_23-1; M176/2_24-2; M176/2_4-2; M176/2_5-2; M176/2_6-3; M176/2_7-2; M176/2_8-3; M176/2_9-2; Meteor (1986); Mid-Atlantic Ridge; Neon-20; noble gas; Sample code/label; South Atlantic Ocean; Station label; δ Helium-3; δ Neon-22
    Type: Dataset
    Format: text/tab-separated-values, 2086 data points
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  • 3
    Publication Date: 2024-01-04
    Description: This dataset contains measured isotopic compositions of noble gases (helium and neon) of water samples collected during the METEOR expedition (M176/2) between Sep 1st and Oct 6th, 2021 on the Rainbow hydrothermal field, Mid-Atlantic Ridge. Seawater samples for noble gases were collected in a copper pipe, which was connected to the Niskin bottles, with water flowing until bubbles in the tube were removed. While the water was flowing, the pipe was closed using an electrical drill and a ratchet to ensure it is tight enough. Helium and neon isotopes were analyzed at the University of Bremen, using the methods described by Sültenfuß et al. (2009). In detail, helium and neon were separated from other gases with a cryogenic system at 25 K. A fraction (3 %) of separated gases was diverted into the quadrupole mass spectrometer (QMS) (Balzers QMG112a®) to measure helium and neon. Upon raising the trap temperature to 45 K, helium and neon were released into the main sector field mass spectrometer (SMS) to measure the concentrations of 3He, 4He, and 20Ne. The measured concentrations were in a unit of CCSTP (cubic centimeters at standard temperature and pressure). delta3He (δ3He, in ‰) was calculated as: [3He/4He(sample)/3He/4He(air)-1]*100, and delta22Ne (δ22Ne, in ‰) was calculated as: [22Ne/20Ne(sample)/22Ne/20Ne(air)-1]*100. The background 3He (2.38 fM) in the deep ocean was calculated from the background δ3He (~ -1.7%) and equilibrium helium concentrations (~ 1.75 nM) at the salinity (35 PSU) and temperature (~ 3.5 °C) ranges of the seawater samples. The excess of 3He (3Hexs) was then calculated by extracting the measured 3He concentrations with the background 3He level.
    Keywords: Bottle number; CTD/Rosette, ultra clean; CTD-UC; Date/Time of event; Depth, bathymetric; DEPTH, water; Event label; GEOTRACES; Global marine biogeochemical cycles of trace elements and their isotopes; GPF 21‐2_049, Rainbow Plume; Helium-3; Helium-3/Helium-4; Helium-4; hydrothermal systems; LATITUDE; LONGITUDE; M176/2; M176/2_10-3; M176/2_12-1; M176/2_13-3; M176/2_14-3; M176/2_15-3; M176/2_16-1; M176/2_17-2; M176/2_18-2; M176/2_19-2; M176/2_21-2; M176/2_23-1; M176/2_24-2; M176/2_4-2; M176/2_5-2; M176/2_6-3; M176/2_7-2; M176/2_8-3; M176/2_9-2; Meteor (1986); Mid-Atlantic Ridge; Neon-20; Neon-20/Helium-4; noble gas; Sample code/label; South Atlantic Ocean; Station label; δ Helium-3; δ Neon-22
    Type: Dataset
    Format: text/tab-separated-values, 1767 data points
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  • 4
    Publication Date: 2024-03-22
    Description: We present high‐resolution profiles of dissolved, labile, and total particulate trace metals (TMs) on the Northeast Greenland shelf from GEOTRACES cruise GN05 in August 2016. Combined with radium isotopes, stable oxygen isotopes, and noble gas measurements, elemental distributions suggest that TM dynamics were mainly regulated by the mixing between North Atlantic‐derived Intermediate Water, enriched in labile particulate TMs (LpTMs), and Arctic surface waters, enriched in Siberian shelf‐derived dissolved TMs (dTMs; Co, Cu, Fe, Mn, and Ni) carried by the Transpolar Drift. These two distinct sources were delineated by salinity‐dependent variations of dTM and LpTM concentrations and the proportion of dTMs relative to the total dissolved and labile particulate ratios. Locally produced meltwater from the Nioghalvfjerdsbræ (79NG) glacier cavity, distinguished from other freshwater sources using helium excess, contributed a large pool of dTMs to the shelf inventory. Localized peaks in labile and total particulate Cd, Co, Fe, Mn, Ni, Cu, Al, V, and Ti in the cavity outflow, however, were not directly contributed by submarine melting. Instead, these particulate TMs were mainly supplied by the re‐suspension of cavity sediment particles. Currently, Arctic Ocean outflows are the most important source of dFe, dCu, and dNi on the shelf, while LpTMs and up to 60% of dMn and dCo are mainly supplied by subglacial discharge from the 79NG cavity. Therefore, changes in the cavity‐overturning dynamics of 79NG induced by glacial retreat, and alterations in the transport of Siberian shelf‐derived materials with the Transport Drift may shift the shelf dTM‐LpTM stoichiometry in the future.
    Description: Plain Language Summary: Trace metals (TMs) including cobalt (Co), iron (Fe), manganese (Mn), copper (Cu), and nickel (Ni) are essential micronutrients for marine productivity. The Northeast Greenland shelf is a climatically sensitive region, influenced by both outflowing Arctic waters and local glacier melting. We lack knowledge on how these Arctic surface waters affect TM dynamics on the Greenland shelf and how climatic shifts may influence TM dynamics. Here, we distinguish local submarine meltwater from Arctic surface waters using distinct tracers; noble gases and radium isotopes. We show that the TM dynamics on the shelf are largely controlled by the intrusion of Arctic surface waters which creates a near‐surface plume of dissolved and labile particulate TMs. Conversely, submarine meltwater creates a subsurface plume enriched in dissolved TMs but depleted in particulate TMs, which is exported from underneath a floating ice tongue. In the future, increasing Arctic river discharge and local glacial melting may both significantly change shelf micronutrient ratios demonstrating downstream impacts of a changing cryosphere on marine biogeochemical cycles.
    Description: Key Points: The overall dissolved and particulate trace metal (TM) dynamics were mainly regulated by the mixing with Arctic surface waters. Resuspension of cavity sediments is a major localized source of labile and total particulate Cd, Co, Fe, Mn, Ni, Cu, Al, V, and Ti. Whilst dissolved and particulate TMs are mostly coupled on the Greenland shelf, cavity outflow decouples both phases.
    Description: Kuwait Institute for Scientific Research
    Description: Deutsche Forschungsgemeinschaft
    Description: https://doi.pangaea.de/10.1594/PANGAEA.871030
    Description: https://doi.pangaea.de/10.1594/PANGAEA.871030
    Description: https://doi.pangaea.de/10.1594/PANGAEA.871028
    Description: https://doi.pangaea.de/10.1594/PANGAEA.905347
    Description: https://doi.pangaea.de/10.1594/PANGAEA.933431
    Description: https://doi.pangaea.de/10.1594/PANGAEA.948466
    Description: https://doi.pangaea.de/10.1594/PANGAEA.936029
    Description: https://doi.pangaea.de/10.1594/PANGAEA.936027
    Description: https://doi.org/10.1594/PANGAEA.931336
    Keywords: ddc:551.9 ; Arctic ; trace metals ; labile particulate ; glacier ; meltwater ; GEOTRACES
    Language: English
    Type: doc-type:article
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  • 5
    Publication Date: 2023-02-08
    Description: Highlights • The vent fluids discharged from the Lutao hydrothermal field experienced low-degree subcritical phase separation. • The temperature and chemical compositions of the vent fluids were modulated by tides. • The time delay between tides and the response of hydrothermal system was about 3 h. • The typhoon “Fung-wong” cooled the reaction zone and decreased the degree of phase separation. • The hydrothermal system began to recover after the typhoon passed by. Abstract The Lutao hydrothermal field is an intertidal arc-volcanic system located offshore southeast Taiwan, hosting a Zhudanqu (ZDQ) vent and a Huwaichi (HWC) spring with strongly contrasting fluid chemistry. Low Mg, moderately enriched Cl, and H+ with respect to seawater indicate that the ZDQ endmember was derived from the brine phase that was formed during low-degree subcritical phase separation. In contrast, the endmember for the HWC vent fluids is related to the vapor phase. Temperature and pressure of the phase separation were estimated as ~150 °C and ~7 bar, respectively. The water/rock ratio was roughly calculated as about 2. The Lutao hydrothermal system was slightly affected by semi-diurnal tides, by some combination of tidal loading and tidal currents. The time delay between tides and the response of the hydrothermal system was about 3 h. While freshwater was almost absent in the HWC vent fluids at normal conditions, the typhoon “Fung-wong” on Sep 21st, 2014, led to intrusions of freshwater into the vent fluids with a percentage of ~16%. Both the ZDQ and the HWC endmember compositions showed some changes after the typhoon event, suggesting a cooling of the reaction zone. After the typhoon passed by, the hydrothermal system began to recover, evidenced by increasing percentages of the HWC endmember and decreasing freshwater contributions. The flux of the HWC endmember was estimated as 460–560 L h−1 based on these observations. This study, for the first time, reports a shallow-depth tidal-influenced hydrothermal system that was temporarily cooled by a tropical storm.
    Type: Article , PeerReviewed
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  • 6
    Publication Date: 2023-02-08
    Description: Seawater Mg:Ca and Sr:Ca ratios are biogeochemical parameters reflecting the Earth-ocean-atmosphere dynamic exchange of elements. The ratios' dependence on the environment and organisms' biology facilitates their application in marine sciences. Here, we present a measured single-laboratory dataset, combined with previous data, to test the assumption of limited seawater Mg:Ca and Sr:Ca variability across marine environments globally. High variability was found in open-ocean upwelling and polar regions, shelves/neritic and river-influenced areas, where seawater Mg:Ca and Sr:Ca ratios range from ∼4.40 to 6.40 mmol:mol and ∼6.95 to 9.80 mmol:mol, respectively. Open-ocean seawater Mg:Ca is semiconservative (∼4.90 to 5.30 mol:mol), while Sr:Ca is more variable and nonconservative (∼7.70 to 8.80 mmol:mol); both ratios are nonconservative in coastal seas. Further, the Ca, Mg, and Sr elemental fluxes are connected to large total alkalinity deviations from International Association for the Physical Sciences of the Oceans (IAPSO) standard values. Because there is significant modern seawater Mg:Ca and Sr:Ca ratios variability across marine environments we cannot absolutely assume that fossil archives using taxa-specific proxies reflect true global seawater chemistry but rather taxa- and process-specific ecosystem variations, reflecting regional conditions. This variability could reconcile secular seawater Mg:Ca and Sr:Ca ratio reconstructions using different taxa and techniques by assuming an error of 1 to 1.50 mol:mol, and 1 to 1.90 mmol:mol, respectively. The modern ratios' variability is similar to the reconstructed rise over 20 Ma (Neogene Period), nurturing the question of seminonconservative behavior of Ca, Mg, and Sr over modern Earth geological history with an overlooked environmental effect.
    Type: Article , PeerReviewed , info:eu-repo/semantics/article
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  • 7
    Publication Date: 2024-02-07
    Description: Highlights • Aerobic oxidation of alkanes was observed in hydrothermal fluids during storage. • The residual CH4 shows the highest ever reported δ13C of up to +243‰. • The εC for C1, C2, and C3 oxidation were −37.1‰, −14.8‰ and −4.7‰, respectively. • The εH for methane was −281 ± 187‰, while the Λ value was 8.4 ± 4.6. • Aerobic oxidation could produce carbon isotope reversal of the residual alkanes. Aerobic oxidation of short-chain alkanes was observed in gas samples from the Lutao intertidal hydrothermal vents in Taiwan, during storage at 20 °C for up to 29 months without adding bacterial strains and replenishing substrates. The carbon isotope fractionation factors (εC) of methane (C1), ethane (C2), and propane (C3), were calculated using the Rayleigh fractionation equation to be −37.1 ± 7.5‰, −14.8 ± 4.8‰, and −4.7 ± 5.2‰, respectively. The hydrogen isotope fractionation factor (εH) of methane was determined to be −281 ± 187‰. DNA sequencing of the 16S rRNA gene in the vent fluids suggests that aerobic oxidation is dominated by methanotrophs of the genera Methylomicrobium and Methylophaga, which use the ribulose monophosphate pathway (RuMP). The degrees of isotope fractionation (εC and εH values) herein are larger than previously reported values, possibly due to the limited O2 supply and low abundance of aerobic methane-oxidizing bacteria in the experiments. Since the fractionation factor of methane is higher than those of ethane and propane, the aerobic oxidation of thermogenic or microbial alkanes could produce a carbon isotope reversal, which is frequently noted as a trait of abiotic hydrocarbons. This work demonstrates that in addition to anaerobic microbial oxidation, aerobic oxidation with a low cell density can also produce significant isotope fractionation of alkanes in geological closed/semi-closed environments and open flow reaction systems that are characterized by moderate temperatures and a limited supply of substrates and O2; these environments include cold seeps, mud volcanoes, and low-temperature hydrothermal plumes/aquifers/reservoirs.
    Type: Article , PeerReviewed
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  • 8
    Publication Date: 2024-02-07
    Description: Dissolved (〈0.2 μm) trace metals (dTMs) including iron (Fe), manganese (Mn), and cobalt (Co) are micronutrients that (co-) limit phytoplankton growth in many ocean regions. Here, we present the spatial and seasonal distributions of dFe, dMn, and dCo on the Northeast Atlantic continental margin (Celtic Sea), along a transect across the shelf and two off-shelf transects along a canyon and a spur. Waters on the continental shelf showed much higher dTM concentrations (dFe 0.07–6.50 nmol L−1, average 1.41 ± 0.96 nmol L−1, n = 138; dMn 0.868–14.8 nmol L−1, 2.75 ± 2.37 nmol L−1, n = 148; dCo 54.8–217 pmol L−1, 109 ± 32 pmol L−1, n = 144) than on the slope (dFe 0.03–1.90 nmol L−1, 0.65 ± 0.43 nmol L−1, n = 454; dMn 0.223–1.14 nmol L−1, 0.58 ± 0.20 nmol L−1, n = 458; dCo 27.3–122 pmol L−1, 71.7 ± 11.7 pmol L−1, n = 441), attributed to strong dTM contributions from a low-salinity endmember, i.e., riverine discharge. Benthic sedimentary input via reductive dissolution (especially for dFe and dMn), delineated by short-lived radium (Ra) isotopic activities (223Raxs and 224Raxs), was only prominent at a station (Site A) characterized by fine sediments. On the continental slope, dMn levels at depth were mainly determined by the formation of insoluble Mn oxides and the intrusion of Mediterranean Outflow Waters. In contrast, dFe and dCo concentrations at depth were balanced by the regeneration from remineralization of sinking organic particles and scavenging removal. In addition, bottom and intermediate nepheloid layers along the slope illustrated both elevated dTM concentrations and Ra isotopic activities. The presence of nepheloid layers is especially significant along the canyon transect relative to the spur transect, demonstrating the importance of slope topography on the off-shelf transport of dTMs into the Northeast Atlantic Ocean. As a seasonal stratified shelf sea, dTMs and nutrients showed synchronized seasonal variations on the shelf, indicating the influence of biological processes in addition to source effects. Surface dFe and dCo were depleted in summer due to enhanced biological uptake, while sub-surface dFe and dCo were elevated in summer and autumn ascribed to the remineralization of sinking organic particles. In contrast, surface dMn levels were predominantly controlled by the seasonal variations in photoreduction, while sub-surface dMn concentrations were relatively constant throughout the year. The combined effects of fluvial and benthic sources, topographical controls, and biological processes shape the seasonal variations of dTM distributions. Such seasonal variations in dTMs and biological activities can affect the biological carbon pump on the Northeast Atlantic continental margin, and may further influence the carbon cycle in the Atlantic Ocean via the dynamic dTM exchange between continental margins and the open ocean.
    Type: Article , PeerReviewed
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  • 9
    Publication Date: 2024-02-07
    Description: The chemical and isotopic characteristics of calcium (Ca) in subduction zones are closely related to the budget of Ca and carbon cycles. Here we investigate the ultra-high Ca concentrations that characterize the hydrothermal fluids discharged from two types of vents, named the Zhudanqu brine vent (ZDQ) and the Huwaichi vapor spring (HWC), in the Lutao hydrothermal system at the north Luzon arc. The Ca concentrations of up to 159 mM and Ca/Cl ratio of up to 0.26 in the ZDQ vent fluids are possibly the highest ever reported for Ca enrichment in global seawater-circulated hydrothermal/geothermal systems. The differences in chemical compositions between the ZDQ and the HWC vent fluids are primary controlled by subcritical phase separation. The brine phase constitutes the ZDQ vent fluids, while the HWC vent fluids represent mixtures of the vapor phase and seawater. Both the vapor and the brine phases exhibit similar δ44/40Ca values (0.72 ± 0.05‰), suggesting no significant Ca isotope fractionation has occurred during phase separation. The hydrothermal endmember before phase separation (the “Lutao endmember”) presents depletions of 213 ± 15 mM of Na, 24.4 ± 0.4 mM of SO42−, and 10.2 mM of K, and enrichment of 130.2 ± 5.5 mM of Ca with respect to the percolated seawater. The total gained Ca is 154.6 ± 5.9 mM with a δ44/40Ca value of 0.67‰ – 0.77‰ (0.72 ± 0.05‰), considering anhydrite precipitation during hydrothermal circulation. The Holocene raised coral reef is unlikely to contribute substantial Ca into the Lutao system. Much of the gained Ca (111.6 ± 7.5 mM) is produced by high-degree albitization of the Lutao host rock, which is promoted by the low water/rock ratio (~ 2), slightly alkaline conditions, and relatively lower temperature of the Lutao system with respect to most mid-ocean ridge hydrothermal systems. Ca derived from this process inherits the Ca isotopes of plagioclase in the Lutao host rocks (δ44/40Ca = 0.82 ± 0.06‰). According to mass and isotopic balances, the recycled marine carbonate is proposed to contribute 43 ± 13.4 mM Ca with a δ44/40Ca value of 0.46−0.63+0.35‰ into the Lutao system. Such isotopically lighter Ca is derived from either pore fluids expulsed from underlying Philippine Sea sediments, or more probably, carbonate-bearing subduction fluids from the subducting South China Sea sediments and slab. The carbonate solubility in the subduction fluids could maintain at 600 mM near the reaction zone. The carbonate-rich fluids were subsequently migrated into the Lutao reaction zone and released an additional 43 ± 13.4 mM Ca via dolomitization. A small amount (~ 9%) addition of carbonate-rich fluids would not significantly change the budgets of Na, Mg, and Cl but could generate substantial Ca enrichment and Ca isotopic variations.
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  • 10
    Publication Date: 2024-02-07
    Description: We present high-resolution profiles of dissolved, labile and total particulate trace metals (TMs) on the Northeast Greenland shelf from GEOTRACES cruise GN05 in August 2016. Combined with radium isotopes, stable oxygen isotopes, and noble gas measurements, elemental distributions suggest that TM dynamics were mainly regulated by the mixing between North Atlantic-derived Intermediate Water, enriched in labile particulate TMs (LpTMs), and Arctic surface waters, enriched in Siberian shelf-derived dissolved TMs (dTMs; Co, Cu, Fe, Mn, and Ni) carried by the Transpolar Drift. These two distinct sources were delineated by salinity-dependent variations of dTM and LpTM concentrations and the proportion of dTMs relative to the total dissolved and labile particulate ratios. Locally produced meltwater from the Nioghalvfjerdsbræ (79NG) glacier cavity, distinguished from other freshwater sources using helium excess, contributed a large pool of dTMs to the shelf inventory. Localized peaks in labile and total particulate Cd, Co, Fe, Mn, Ni, Cu, Al, V, and Ti in the cavity outflow, however, were not directly contributed by submarine melting. Instead, these particulate TMs were mainly supplied by the re-suspension of cavity sediment particles. Currently, Arctic Ocean outflows are the most important source of dFe, dCu and dNi on the shelf, while LpTMs and up to 60% of dMn and dCo are mainly supplied by subglacial discharge from the 79NG cavity. Therefore, changes in the cavity-overturning dynamics of 79NG induced by glacial retreat, and alterations in the transport of Siberian shelf-derived materials with the Transport Drift may shift the shelf dTM-LpTM stoichiometry in the future. Key Points The overall dissolved and particulate trace metal dynamics were mainly regulated by the mixing with Arctic surface waters Resuspension of cavity sediments is a major localized source of labile and total particulate Cd, Co, Fe, Mn, Ni, Cu, Al, V, and Ti Whilst dissolved and particulate trace metals are mostly coupled on the Greenland shelf, cavity outflow decouples both phases
    Type: Article , PeerReviewed , info:eu-repo/semantics/article
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