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 August 28, 2025

Title: Distribution and Cycling of Nickel and Nickel Isotopes in the Pacific Ocean
Abstract Nickel stable isotopes (δ60Ni) provide insight to Ni biogeochemistry in the modern and past oceans. Here, we present the first Pacific Ocean high‐resolution dissolved Ni concentration and δ60Ni data, from the US GEOTRACES GP15 cruise. As in other ocean basins, increases in δ60Ni toward the surface ocean are observed across the entire transect, reflecting preferential biological uptake of light Ni isotopes, however the observed magnitude of fractionation is larger in the tropical Pacific than the North Pacific Subtropical Gyre. Such surface ocean fractionation by phytoplankton should accumulate isotopically lighter Ni in the deep Pacific, yet we find that North Pacific deep ocean δ60Ni is similar to previously reported values from the deep Atlantic. Finally, we find that seawater dissolved δ60Ni in regions with hydrothermal input can be either higher or lower than background deep ocean δ60Ni, depending on vent geochemistry and proximity.  more » « less
Award ID(s):
1737136
PAR ID:
10542225
Author(s) / Creator(s):
; ; ; ; ; ; ; ; ;
Publisher / Repository:
AGU
Date Published:
Journal Name:
Geophysical Research Letters
Volume:
51
Issue:
16
ISSN:
0094-8276
Format(s):
Medium: X
Sponsoring Org:
National Science Foundation
More Like this
  1. Abstract The North Pacific has played an important role in ongoing discussions on the origin of the global correlation between oceanic dissolved Zn and Si, while data in the North Pacific have remained sparse. Here, we present dissolved Zn and δ66Zn data from the US GEOTRACES GP15 meridional transect along 152°W from Alaska to the South Pacific. In the south (<20°N) Zn and Si exhibit a tight linear correlation reflecting strong Southern Ocean influence, while in the north (>20°N) an excess of Zn relative to Si in upper and intermediate waters is due to regeneration of Zn together with PO4. Using a mechanistic model, we show that reversible scavenging is required as an additional process transferring Zn from the upper to the deep ocean, explaining the deep Zn maximum below the PO4maximum. This mechanism applied for reversible scavenging also provides an explanation for the observed isotope distribution: (a) fractionation during ligand binding and subsequent removal of residual heavy Zn in the upper ocean, drives the upper ocean toward lower δ66Zn, while (b) release of heavy Zn then coincides with the PO4maximum where carrier particles regenerate, causing a mid‐depth δ66Zn maximum. In the upper ocean, seasonal physical stratification is an additional important process influencing shallow δ66Zn signals. At the global scale, this mechanism invoking fractionation during ligand binding coupled with reversible scavenging offers a global explanation for isotopically light Zn at shallow depths and corresponding elevated mid‐depth δ66Zn signals, seen dominantly in ocean regions away from strong Southern Ocean control. 
    more » « less
  2. Abstract Despite the Pacific being the location of the earliest seawater Cd studies, the processes which control Cd distributions in this region remain incompletely understood, largely due to the sparsity of data. Here, we present dissolved Cd and δ114Cd data from the US GEOTRACES GP15 meridional transect along 152°W from the Alaskan margin to the equatorial Pacific. Our examination of this region's surface ocean Cd isotope systematics is consistent with previous observations, showing a stark disparity between northern Cd‐rich high‐nutrient low‐chlorophyll waters and Cd‐depleted waters of the subtropical and equatorial Pacific. Away from the margin, an open system model ably describes data in Cd‐depleted surface waters, but atmospheric inputs of isotopically light Cd likely play an important role in setting surface Cd isotope ratios (δ114Cd) at the lowest Cd concentrations. Below the surface, Southern Ocean processes and water mass mixing are the dominant control on Pacific Cd and δ114Cd distributions. Cd‐depleted Antarctic Intermediate Water has a far‐reaching effect on North Pacific intermediate waters as far as 47°N, contrasting with northern‐sourced Cd signatures in North Pacific Intermediate Water. Finally, we show that the previously identified negative Cd* signal at depth in the North Pacific is associated with the PO4maximum and is thus a consequence of an integrated regeneration signal of Cd and PO4at a slightly lower Cd:P ratio than the deep ocean ratio (0.35 mmol mol−1), rather than being related to in situ removal processes in low‐oxygen waters. 
    more » « less
  3. Abstract Distinctively‐light isotopic signatures associated with Fe released from anthropogenic activity have been used to trace basin‐scale impacts. However, this approach is complicated by the way Fe cycle processes modulate oceanic dissolved Fe (dFe) signatures (δ56Fediss) post deposition. Here we include dust, wildfire, and anthropogenic aerosol Fe deposition in a global ocean biogeochemical model with active Fe isotope cycling, to quantify how anthropogenic Fe impacts surface ocean dFe and δ56Fediss. Using the North Pacific as a natural laboratory, the response of dFe, δ56Fediss, and primary productivity are spatially and seasonally variable and do not simply follow the footprint of atmospheric deposition. Instead, the effect of anthropogenic Fe is regulated by the biogeochemical regime, specifically the degree of Fe limitation and rates of primary production. Overall, we find that while δ56Fedissdoes trace anthropogenic input, the response is muted by fractionation during phytoplankton uptake, but amplified by other isotopically‐light Fe sources. 
    more » « less
  4. Abstract Dissolved organic nitrogen (DON) is the dominant form of fixed nitrogen in most low and middle latitude ocean surface waters. Here, we report measurements of DON isotopic composition (δ15N) from the west South China Sea (SCS), with the goal of providing new insight into DON cycling. The concentration of DON in the surface ocean is correlated (r = 0.70,p < 0.0001) with chlorophyllaconcentration, indicating DON production in these surface waters. The concentration and δ15N of DON fall in a relatively narrow range in the surface ocean (4.6 ± 0.1 μM and 4.3 ± 0.2‰ vs. air, respectively; ±SD), similar to other ocean regions. The mean DON δ15N above 50 m (4.5 ± 0.3‰) is similar to the δ15N of nitrate in the “shallow subsurface” (i.e., immediately below the euphotic zone; 4.6 ± 0.2‰) but is higher than the δ15N of suspended particles in the surface ocean (~2.3‰). This set of isotopic relationships has been observed previously (e.g., in the oligotrophic North Atlantic and North Pacific) and can be explained by the cycling of N between particulate organic nitrogen (PON), DON, and ammonium, in which an isotope effect associated with DON degradation preferentially concentrates15N in DON. Consistent with this view, a negative correlation (r = 0.70) between the concentration and the δ15N of DON is observed in the upper 75 m, suggesting an isotope effect of ~4.9 ± 0.4‰ for DON degradation. Comparing the DON δ15N data from the SCS with other regions, we find that the δ15N difference between euphotic zone DON and shallow subsurface nitrate δ15N (Δδ15N(DON‐NO3)) rises from ocean regions of inferred net DON production to regions of net DON consumption, with the SCS representing an intermediate case. 
    more » « less
  5. Abstract During the last deglaciation Earth’s climate experienced strong and abrupt variations, resulting in major changes in global temperature, sea level, and ocean circulation. Although proxy records have significantly improved our understanding of climate during this period, questions remain regarding the connection between ocean circulation evolution and resulting geotracer distributions, including those of deep waters in the Pacific. Here we use the C‐iTRACE simulation, a transient ocean‐only, isotope‐enabled version of the Community Earth System Model, to better understand deglacial deep Pacific radiocarbon evolution in the context of circulation and reservoir age changes. Throughout the deglaciation, the Pacific Ocean circulation in C‐iTRACE responds strongly to glacial meltwater forcing, leading to large changes in deep Pacific Δ14C age. A multi‐millennial weakening of the overturning circulation from 20 to 15 ka BP leads to increases in deep Pacific Δ14C ages, but from 20 to 18 ka BP, nearly half (40%–60%) of this aging is controlled by changing surface reservoir age, corroborating previous studies showing that Δ14C is not solely a circulation age tracer. As the deglaciation proceeds, circulation change controls progressively more of the Δ14C age, accounting for more than 75% of it across the deep Pacific from 15 to 8 ka BP. 
    more » « less