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The Greenland Ice Sheet is losing mass at an accelerating pace, increasing its contribution to the freshwater input into the Nordic Seas and the subpolar North Atlantic. It has been proposed that this increased freshwater may impact the Atlantic Meridional Overturning Circulation by affecting the stratification of the convective regions of the North Atlantic and Nordic Seas. Observations of the transformation and pathways of meltwater from the Greenland Ice Sheet on the continental shelf and in the gyre interior, however, are lacking. Here, we report on noble gas derived observations of submarine meltwater distribution and transports in the East and West Greenland Current Systems of southern Greenland and around Cape Farewell. In southeast Greenland, submarine meltwater is concentrated in the East Greenland Coastal Current core with maximum concentrations of 0.8%, thus significantly diluted relative to fjord observations. It is found in water with density ranges from 1,024 to 1027.2 kg m⁻³and salinity from 30.6 to 34, which extends as deep as 250 m and as far offshore as 60 km on the Greenland shelf. Submarine meltwater transport on the shelf averages 5.0 ± 1.6 mSv which, if representative of the mean annual transport, represents 60%–80% of the total solid ice discharge from East Greenland and suggests relatively little offshore export of meltwater east and upstream of Cape Farewell. The location of the meltwater transport maximum shifts toward the shelfbreak around Cape Farewell, positioning the meltwater for offshore flux in regions of known cross‐shelf exchange along the West Greenland coast.

 

Gas exchange between the atmosphere and ocean interior profoundly impacts global climate and biogeochemistry. However, our understanding of the relevant physical processes remains limited by a scarcity of direct observations. Dissolved noble gases in the deep ocean are powerful tracers of physical air-sea interaction due to their chemical and biological inertness, yet their isotope ratios have remained underexplored. Here, we present high-precision noble gas isotope and elemental ratios from the deep North Atlantic (~32°N, 64°W) to evaluate gas exchange parameterizations using an ocean circulation model. The unprecedented precision of these data reveal deep-ocean undersaturation of heavy noble gases and isotopes resulting from cooling-driven air-to-sea gas transport associated with deep convection in the northern high latitudes. Our data also imply an underappreciated and large role for bubble-mediated gas exchange in the global air-sea transfer of sparingly soluble gases, including O 2 , N 2 , and SF 6 . Using noble gases to validate the physical representation of air-sea gas exchange in a model also provides a unique opportunity to distinguish physical from biogeochemical signals. As a case study, we compare dissolved N 2 /Ar measurements in the deep North Atlantic to physics-only model predictions, revealing excess N 2 from benthic denitrification in older deep waters (below 2.9 km). These data indicate that the rate of fixed N removal in the deep Northeastern Atlantic is at least three times higher than the global deep-ocean mean, suggesting tight coupling with organic carbon export and raising potential future implications for the marine N cycle. 

Abstract. Over the past decade, the GEOTRACES and wider trace metalgeochemical community has made substantial contributions towardsconstraining the marine cobalt (Co) cycle and its major biogeochemicalprocesses. However, few Co speciation studies have been conducted in theNorth and equatorial Pacific Ocean, a vast portion of the world's oceans byvolume and an important end-member of deep thermohaline circulation.Dissolved Co (dCo) samples, including total dissolved and labile Co, weremeasured at-sea during the GEOTRACES Pacific Meridional Transect (GP15) expedition along the 152∘ W longitudinal from 56∘ N to20∘ S. Along this transect, upper-ocean dCo (σ0<26) was linearly correlated with dissolved phosphate (slope = 82±3, µmol : mol) due to phytoplankton uptake and remineralization.As depth increased, dCo concentrations became increasingly decoupled fromphosphate concentrations due to co-scavenging with manganese oxide particlesin the mesopelagic. The transect revealed an organically bound coastalsource of dCo to the Alaskan Stream associated with low-salinity waters. Anintermediate-depth hydrothermal flux of dCo was observed off the Hawaiiancoast at the Loihi Seamount, and the elevated dCo was correlated withpotential xs3He at and above the vent site; however, the Loihi Seamountlikely did not represent a major source of Co to the Pacific basin. Elevatedconcentrations of dCo within oxygen minimum zones (OMZs) in the equatorialNorth and South Pacific were consistent with the suppression of oxidativescavenging, and we estimate that future deoxygenation could increase the OMZdCo inventory by 18 % to 36 % over the next century. In Pacific Deep Water(PDW), a fraction of elevated ligand-bound dCo appeared protected fromscavenging by the high biogenic particle flux in the North Pacific basin.This finding is counter to previous expectations of low dCo concentrationsin the deep Pacific due to scavenging over thermohaline circulation.Compared to a Co global biogeochemical model, the observed transectdisplayed more extreme inventories and fluxes of dCo than predicted by themodel, suggesting a highly dynamic Pacific Co cycle. 

The noble gas signature of incoming Pacific Bottom Water (PBW), when compared to North Atlantic Deep Water, indicates the addition of 450 ± 70 GT a⁻¹glacial melt water to form AABW and subsequently PBW. The downstream evolution of this signature between the southern (20°S to equator) and northern (25°–45°N) bottom waters indicates a decrease in sea level pressure around Antarctica over the past two millennia. Vertical profiles of noble gases in the deep Pacific show exponential relationships with depth with scale heights identical to temperature and salinity. Unlike the other noble gases, helium isotopes show evidence of mid‐depth injection of non‐atmospheric helium. Using observed deviations from exponential behavior, we quantify its magnitude and isotope ratio. There is a clear latitude trend in the isotope ratio of this added helium that decreases from a high exceeding 9 R_A(atmospheric³He/⁴He ratio) in the south to around 8 R_Anear the equator. North of 30–40°N, it systematically decreases northward to a low of ∼2 R_Anorth of 50°N. This decline results from a combination of northward decline in seafloor spreading, release of radiogenic helium from increased sediment thickness, and the possible emission of radiogenic helium through cold seeps along the Alaskan and North American margins. Finally, we derive an improved method of computing the excess helium isotope concentrations and that the distributions of bottom water³He_XS/⁴He_XSare consistent with what is known about bottom water flow patterns and the input of low³He/⁴He sedimentary helium.

 

Using a recently compiled global marine data set of dissolved helium isotopes and helium and neon concentrations, we make an estimate of the inventory of hydrothermal³He in the Southern Ocean to be 4.9 ± 0.6 × 10⁴ moles. Under the assumption that the bulk of the hydrothermally sourced³He is upwelled there, we use recent estimates of the global hydrothermal³He flux to determine ane‐folding residence time of 99 ± 18 years, depending on assumptions of water mass and upwelling boundaries. Our estimate is within the broad range of values obtained from recent Southern Ocean circulation models.

 

Abstract. Tritium and helium isotope data provide key information on oceancirculation, ventilation, and mixing, as well as the rates of biogeochemicalprocesses and deep-ocean hydrothermal processes. We present here globaloceanic datasets of tritium and helium isotope measurements made by numerousresearchers and laboratories over a period exceeding 60 years. The dataset'sDOI is https://doi.org/10.25921/c1sn-9631, and the data are available athttps://www.nodc.noaa.gov/ocads/data/0176626.xml (last access: 15 March2019) or alternatelyhttp://odv.awi.de/data/ocean/jenkins-tritium-helium-data-compilation/(last access: 13 March 2019) and includes approximately 60 000 valid tritiummeasurements, 63 000 valid helium isotope determinations, 57 000 dissolvedhelium concentrations, and 34 000 dissolved neon concentrations. Somequality control has been applied in that questionable data have been flaggedand clearly compromised data excluded entirely. Appropriate metadata havebeen included, including geographic location, date, and sample depth. Whenavailable, we include water temperature, salinity, and dissolved oxygen. Dataquality flags and data originator information (including methodology) arealso included. This paper provides an introduction to the dataset along withsome discussion of its broader qualities and graphics.