Abstract Distributions of the natural radionuclide210Po and its grandparent210Pb along the GP15 Pacific Meridional Transect provide information on scavenging rates of reactive chemical species throughout the water column and fluxes of particulate organic carbon (POC) from the primary production zone (PPZ).210Pb is in excess of its grandparent226Ra in the upper 400–700 m due to the atmospheric flux of210Pb. Mid‐water210Pb/226Ra activity ratios are close to radioactive equilibrium (1.0) north of ∼20°N, indicating slow scavenging, but deficiencies at stations near and south of the equator suggest more rapid scavenging associated with a “particle veil” located at the equator and hydrothermal processes at the East Pacific Rise. Scavenging of210Pb and210Po is evident in the bottom 500–1,000 m at most stations due to enhanced removal in the nepheloid layer. Deficits in the PPZ of210Po (relative to210Pb) and210Pb (relative to226Ra decay and the210Pb atmospheric flux), together with POC concentrations and particulate210Po and210Pb activities, are used to calculate export fluxes of POC from the PPZ.210Po‐derived POC fluxes on large (>51 μm) particles range from 15.5 ± 1.3 mmol C/m2/d to 1.5 ± 0.2 mmol C/m2/d and are highest in the Subarctic North Pacific;210Pb‐derived fluxes range from 6.7 ± 1.8 mmol C/m2/d to 0.2 ± 0.1 mmol C/m2/d. Both210Po‐ and210Pb‐derived POC fluxes are greater than those calculated using the234Th proxy, possibly due to different integration times of the radionuclides, considering their different radioactive mean‐lives and scavenging mean residence times. 
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                            Measuring bismuth‐210, its parent, and daughter in aquatic systems
                        
                    
    
            Abstract 210Bi (t1/2: 5.01 d)—the daughter of210Pb and parent of210Po—has rarely been measured in aquatic systems, and its behavior in the water column is poorly understood. In this article, I present a method for quickly measuring210Pb,210Bi, and210Po in aquatic samples, where (1)210Bi and210Po are scavenged onto an anion solid‐phase extraction disk within 15 min of pretreating the sample; (2) beta decay of210Bi is counted on the disk immediately thereafter; (3)210Po is subsequently removed from the disk and redeposited on a copper plate for α‐spectroscopy; and (4)210Pb is determined via the ingrowth of210Bi. I present decay‐corrected calculations for total, dissolved, and particle‐bound fractions of each nuclide and conclude with an analysis of210Pb,210Bi, and210Po activities in rain,dreissenid(quagga) mussels, and water samples from the Milwaukee Inner Harbor in Lake Michigan. Results show that the loss of lead on the anion solid‐phase extraction disks was negligible (0.2% ± 2.1%; ± 1 SD,n= 4), and the sorption of bismuth was complete (99% ± 2%; ± 1 SD,n= 16). Relative mean absolute deviations of duplicate sample analyses of lake water were 2.4% ± 1.9% for210Pb (geometric mean of total sample activity: 3.0 disintegrations per minute [dpm],n= 6), 7.7% ± 5.8% for210Bi (geometric mean of total sample activity: 2.6 dpm,n= 8), and 2.7% ± 1.7% for210Po (geometric mean of total sample activity: 1.4 dpm,n= 8). 
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                            - Award ID(s):
- 1639865
- PAR ID:
- 10457766
- Publisher / Repository:
- Wiley Blackwell (John Wiley & Sons)
- Date Published:
- Journal Name:
- Limnology and Oceanography: Methods
- Volume:
- 18
- Issue:
- 4
- ISSN:
- 1541-5856
- Page Range / eLocation ID:
- p. 148-162
- Format(s):
- Medium: X
- Sponsoring Org:
- National Science Foundation
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