skip to main content
US FlagAn official website of the United States government
dot gov icon
Official websites use .gov
A .gov website belongs to an official government organization in the United States.
https lock icon
Secure .gov websites use HTTPS
A lock ( lock ) or https:// means you've safely connected to the .gov website. Share sensitive information only on official, secure websites.


This content will become publicly available on April 1, 2026

Title: Mercury Distribution and Speciation Along the U.S. GEOTRACES GP15 Pacific Meridional Transect
Abstract Mercury (Hg) is a bioaccumulative neurotoxin that can concentrate to potentially harmful levels in higher levels of marine food webs following conversion to methylmercury (MeHg). This is of public health concern as seafood is a main protein source for many in the Pacific region. To better understand Hg partitioning and transformations in the Pacific Ocean, Hg species and phases were measured along a meridional section from Alaska to Tahiti in 2018. This allowed the description of Hg concentrations and speciation under a variety of biogeochemical conditions such as the Alaskan shelf, the oligotrophic North Pacific gyre, and near the hydrothermally active Loihi seamount. Filtered HgT concentrations were elevated below 1,000 m near the Loihi Seamount with an average concentration of 1.45 pM, possibly indicating enrichment from hydrothermal venting. Filtered MeHg concentrations were notably higher at depth at the equator and generally lower south of the equator. Total Hg in suspended particles was greatest in the upper 1,000 m near the Alaskan Shelf and decreased in concentration southward. Suspended particle MeHg was greatest in the surface ocean in the upper 300 m near the Intertropical Convergence Zone (ITCZ). For both HgT and MeHg, particle‐associated concentrations appear to be related to organic fraction, and concentrations decreased southward. In general, all measured Hg species had greater concentrations in the northern than southern Pacific Ocean consistent with prior measurements.  more » « less
Award ID(s):
2151677
PAR ID:
10585088
Author(s) / Creator(s):
; ; ; ; ;
Publisher / Repository:
American Geophysical Union
Date Published:
Journal Name:
Journal of Geophysical Research: Oceans
Volume:
130
Issue:
4
ISSN:
2169-9275
Format(s):
Medium: X
Sponsoring Org:
National Science Foundation
More Like this
  1. Abstract As the role of the Greenland Ice Sheet in the Arctic mercury (Hg) budget draws scrutiny, it is crucial to understand mercury cycling in glacial fjords, which control exchanges with the ocean. We present full water column measurements of total mercury (THg) and methylmercury (MeHg) in Sermilik Fjord, a large fjord in southeast Greenland fed by multiple marine-terminating glaciers, whose circulation and water mass transformations have been extensively studied. We show that THg (0.23-1.1 pM) and MeHg (0.02-0.17 pM) concentrations are similar to those in nearby coastal waters, while the exported glacially-modified waters are relatively depleted in inorganic mercury (Hg(II)), suggesting that inflowing ocean waters from the continental shelf are the dominant source of mercury species to the fjord. We propose that sediments initially suspended in glacier meltwaters scavenge particle-reactive Hg(II) and are subsequently buried, making the fjord a net sink of oceanic mercury. 
    more » « less
  2. 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. 
    more » « less
  3. Bluefin tuna (BFT), highly prized among consumers, accumulate high levels of mercury (Hg) as neurotoxic methylmercury (MeHg). However, how Hg bioaccumulation varies among globally distributed BFT populations is not understood. Here, we show mercury accumulation rates (MARs) in BFT are highest in the Mediterranean Sea and decrease as North Pacific Ocean > Indian Ocean > North Atlantic Ocean. Moreover, MARs increase in proportion to the concentrations of MeHg in regional seawater and zooplankton, linking MeHg accumulation in BFT to MeHg bioavailability at the base of each subbasin's food web. Observed global patterns correspond to levels of Hg in each ocean subbasin; the Mediterranean, North Pacific, and Indian Oceans are subject to geogenic enrichment and anthropogenic contamination, while the North Atlantic Ocean is less so. MAR in BFT as a global pollution index reflects natural and human sources and global thermohaline circulation. 
    more » « less
  4. We examined mercury (Hg) accumulation in juvenile and adult subpopulations of Antarctic krill (Euphausia superba) collected west of the Antarctic Peninsula. Samples were collected along a northern cross-shelf transect beginning near Anvers Island and farther south near the sea ice edge in the austral summers of 2011, 2013, 2014, and 2015. Regardless of geographical position, mean concentrations of total Hg and methylmercury (MeHg), the form of Hg that biomagnifies in marine food webs, were significantly higher in juvenile than adult krill in all years. In 2013, juvenile Antarctic krill collected along the coast near Anvers Island had significantly higher MeHg concentrations than krill collected farther offshore, and in 2013 and 2014, coastal juvenile krill exhibited some of the highest MeHg concentrations of all subpopulations sampled. Across all sampling years, collection in northern (sea ice-free) or southern (sea ice edge) transects did not affect MeHg concentrations of juvenile or adult krill, suggesting similar levels and routes of MeHg exposure across the latitudes sampled. Developmental stage, feeding near the coast, and annual variations in sea ice-driven primary and export production were identified as potentially important factors leading to greater MeHg accumulation in juvenile than adult krill. Krill-dependent predators feeding primarily on juveniles may thus accumulate more MeHg than consumers foraging on older krill. These results report MeHg concentrations in Antarctic krill and will be useful for predicting Hg biomagnification in higher-level consumers in this productive Antarctic ecosystem. 
    more » « less
  5. The downward flux of sinking particles is a prominent Hg removal and redistribution process in the ocean; however, it is not well-constrained. Using data from three U.S. GEOTRACES cruises including the Pacific, Atlantic, and Arctic Oceans, we examined the mercury partitioning coefficient, K d , in the water column. The data suggest that the K d varies widely over three ocean basins. We also investigated the effect of particle concentration and composition on K d by comparing the concentration of small-sized (1–51 μm) suspended particulate mass (SPM) as well as its compositional fractions in six different phases to the partitioning coefficient. We observed an inverse relationship between K d and suspended particulate mass, as has been observed for other metals and known as the “particle concentration effect,” that explains much of the variation in K d . Particulate organic matter (POM) and calcium carbonate (CaCO 3 ) dominated the Hg partitioning in all three ocean basins while Fe and Mn could make a difference in some places where their concentrations are elevated, such as in hydrothermal plumes. Finally, our estimated Hg residence time has a strong negative correlation with average log bulk K d , indicating that K d has significant effect on Hg residence time. 
    more » « less