From seasonal cruises in the NE Pacific Ocean during 2017, we (1) determined dissolved organic carbon concentrations; (2) calculated net community production (NCP) from nitrate drawdown; and (3) established relationships between NCP and seasonal dissolved organic carbon (DOC) accumulation in the upper 75 m. The fraction of NCP that accumulated as DOC, hereafter referred to as the net dissolved production ratio, was calculated for several stations during spring and summer. The net dissolved production ratio was about 0.26 at the oceanic station Ocean Station Papa during different seasons and years. Using nitrate concentration profiles obtained from Bio‐Argo floats during 2009–2018 operating near Ocean Station Papa, we calculated NCP at high temporal resolution and then applied the 0.26 constant in order to (4) estimate DOC variability for the 9‐year period. We found strong seasonality near Ocean Station Papa, with NCP maxima during summers ranging from 0.3 to 2.9 mol C/m2 and surface DOC concentrations estimated from 56 μmol/kg in winters to 73 μmol/kg in summers. There was a 10‐fold interannual variability in the seasonally accumulated inventory of DOC, ranging from 0.078 to 0.75 mol C/m2. This study reinforces the value of deploying floats equipped with chemical sensors in order to better understand marine biogeochemical cycles, especially when high resolution data cannot be obtained otherwise. Given that ~26% of NCP accumulates as DOC in the central Gulf of Alaska, the remaining balance of ~74% is available for export as sinking biogenic particles.
Figure S1: An example of how the vertical plankton net works at a given layer.
Between 2013 and 2016, a series of warm events induced by ocean atmosphere oscillations negatively impacted productivity in the northeast Pacific Ocean. For two consecutive winters (2013–2014 and 2014–2015), suppressed wind stress and warm near‐surface ocean temperature anomalies restricted vertical mixing between the surface and underlying nutrient‐enriched waters. Here we assess historical data of sea surface temperature and sea level pressure, along with nearly a decade of biogeochemical float data to evaluate the impact of these warm events on organic carbon production. The first stratified winter experienced little apparent impact on the magnitude of net organic carbon production in the growing season relative to prior years, suggesting an immediate resilience from reduced new nutrients, apparently depending on recycled iron. However, the subsequent winter experienced virtually zero net production; a loss of resilience, perhaps due to net iron removal with export, was evident. We find that consistently enhanced winter stratification decreased carbon production much more so than a single warm winter. This study highlights the sensitivity of marine productivity to ocean atmosphere oscillations, reducing deep ocean carbon sequestration with prolonged ocean warming and stratification.
Abstract. Marine diazotrophs convert dinitrogen (N2) gas into bioavailable nitrogen (N), supporting life in the global ocean. In 2012, the first version of the global oceanic diazotroph database (version 1) was published. Here, we present an updated version of the database (version 2), significantly increasing the number of in situ diazotrophic measurements from 13 565 to 55 286. Data points for N2 fixation rates, diazotrophic cell abundance, and nifH gene copy abundance have increased by 184 %, 86 %, and 809 %, respectively. Version 2 includes two new data sheets for the nifH gene copy abundance of non-cyanobacterial diazotrophs and cell-specific N2 fixation rates. The measurements of N2 fixation rates approximately follow a log-normal distribution in both version 1 and version 2. However, version 2 considerably extends both the left and right tails of the distribution. Consequently, when estimating global oceanic N2 fixation rates using the geometric means of different ocean basins, version 1 and version 2 yield similar rates (43–57 versus 45–63 Tg N yr−1; ranges based on one geometric standard error). In contrast, when using arithmetic means, version 2 suggests a significantly higher rate of 223±30 Tg N yr−1 (mean ± standard error; same hereafter) compared to version 1 (74±7 Tg N yr−1). Specifically, substantial rate increases are estimated for the South Pacific Ocean (88±23 versus 20±2 Tg N yr−1), primarily driven by measurements in the southwestern subtropics, and for the North Atlantic Ocean (40±9 versus 10±2 Tg N yr−1). Moreover, version 2 estimates the N2 fixation rate in the Indian Ocean to be 35±14 Tg N yr−1, which could not be estimated using version 1 due to limited data availability. Furthermore, a comparison of N2 fixation rates obtained through different measurement methods at the same months, locations, and depths reveals that the conventional 15N2 bubble method yields lower rates in 69 % cases compared to the new 15N2 dissolution method. This updated version of the database can facilitate future studies in marine ecology and biogeochemistry. The database is stored at the Figshare repository (https://doi.org/10.6084/m9.figshare.21677687; Shao et al., 2022).
We leverage observations from chemical and bio‐optical sensors mounted on a biogeochemical profiling float in the Northeast Pacific Ocean to quantify the cycling and export potential of distinct biogenic carbon pools, including particulate inorganic carbon (PIC), particulate organic carbon (POC), and dissolved organic carbon (DOC). Year‐round observations reveal complex carbon cycle dynamics among these carbon pools. Net DOC production peaked during bloom initiation, about 3 months prior to the summer peak in POC production. We validate the float estimates of DOC cycling with seasonal accumulation and removal rates derived from ship‐board DOC observations over the same period. By combining chemical and bio‐optical tracers of POC cycling, we estimate the instantaneous POC sinking flux (FPOCsinking ${\mathrm{F}}_{{\text{POC}}_{\text{sinking}}}$). The cooccurrence of DOC consumption and POC production and sinking during fall and winter resolves the regional conundrum of a persistent particle sinking flux observed by sediment traps during a season that is known to be heterotrophic. PIC production is small, and uncertainties are large. By combining float‐based estimates of instantaneous net primary production (NPP) and FPOCsinking ${\mathrm{F}}_{{\text{POC}}_{\text{sinking}}}$, we quantify a real‐time carbon export ratio ([FPOCsinking ${\mathrm{F}}_{{\text{POC}}_{\text{sinking}}}$/NPP] × 100%) for the euphotic zone. Elevated export ratios during summer are associated with an increase in the fraction of particles larger than 100 μm in size. Elevated export ratios during winter are associated with the physical redistribution of particles through seasonal deep mixing. Our study demonstrates how the combined use of multiple sensors on biogeochemical profiling floats can provide more nuanced information about upper ocean carbon cycle dynamics.
No abstract
Measurements of pH and nitrate from the Southern Ocean Carbon and Climate Observations and Modeling array of profiling floats were used to assess the ratios of dissolved inorganic carbon (DIC) and nitrate (NO3) uptake during the spring to summer bloom period throughout the Southern Ocean. Two hundred and forty‐three bloom periods were observed by 115 floats from 30°S to 70°S. Similar calculations were made using the Takahashi surface DIC and nitrate climatology. To separate the effects of atmospheric CO2 exchange and mixing from phytoplankton uptake, the ratios of changes in DIC to nitrate of surface waters (ΔDIC/ΔNO3) were computed in the Biogeochemical Southern Ocean State Estimate (B‐SOSE) model. Phytoplankton uptake of DIC and nitrate are fixed in B‐SOSE at the Redfield Ratio (RR; 6.6 mol C/mol N). Deviations in the B‐SOSE ΔDIC/ΔNO3 must be due to non‐biological effects of CO2 gas exchange and mixing. ΔDIC/ΔNO3 values observed by floats and in the Takahashi climatology were corrected for the non‐biological effects using B‐SOSE. The corrected, in situ biological uptake ratio (C:N) occurs at values similar to the RR, with two major exceptions. North of 40°S biological DIC uptake is observed with little or no change in nitrate giving high C:N. In the latitude band at 55°S, the Takahashi data give a low C:N value, while floats are high. This may be due to a change in CO2 air‐sea exchange in this region from uptake during the Takahashi reference year of 2005 to outgassing of CO2 during the years sampled by floats.
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