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Here we shed light on two mechanisms that stimulate deep particle export via upper-ocean iron fertilization in the Southern Ocean: deep frontal mixing and melting of sea ice. We present data collected a decade apart in the Pacific sector of the Southern Ocean when, serendipitously, seasonal Antarctic ice melt was anomalously low (2008) and anomalously high (2017). In 2008, the low ice melt year, we concluded that vertical mixing of iron into the euphotic zone via deep-mixing fronts was the primary stimulant of export that reached depths of ~1500 meters. This process was evidenced by localized enhancements of dissolved organic carbon (DOC) concentrations up to 4 µmol C kg -1 beneath seven branches of fronts embedded within the Antarctic Circumpolar Current (ACC). We used these enhanced DOC concentrations in the bathypelagic as primary indications of the depths and locations of recent export, as it is a logical residue of such. In 2017, the year in which sea ice melt was anomalously high, we concluded that the main driver of a widespread export event to the seafloor was the lateral influx of iron within the melt. Indications of this event included substantial enhancements of DOC concentrations (2 - 6 µmol C kg -1 ), elevated beam attenuation, and enhanced surface iron concentrations associated with a layer of low salinity water at a nearby station. Further, significant deficits of upper ocean silicic acid during the 2017 occupation indicated that deep export was likely stimulated by an iron-fueled diatom bloom. This analysis highlights the impact of iron supplied from frontal vertical mixing and sea ice melt on export and ultimately for long-term carbon sequestration in the Southern Ocean, as well as the utility of deep DOC enrichments as signatures of particle export. Understanding the impact that ice melt events have on carbon export is crucial given that anomalous events are occurring more often as our climate changes. 

This document describes best practices for analysis of dissolved organic matter (dissolved organic carbon and total dissolved nitrogen) in seawater samples. Included are SOPs for sample collection and storage, details for laboratory analysis using high temperature combustion analysis on Shimadzu TOC analyzers, and suggestions for best practices in quality control and quality assurance. Although written specifically for GO-SHIP oceanographic community practices, many aspects of sample collection and processing are relevant to DOM determination across oceanic regimes and this document aims to provide updated methodology to the wider marine community. 

Marine polymer gels play a critical role in regulating ocean basin scale biogeochemical dynamics. This brief review introduces the crucial role of marine gels as a source of aerosol particles and cloud condensation nuclei (CCN) in cloud formation processes, emphasizing Arctic marine microgels. We review the gel’s composition and relation to aerosols, their emergent properties, and physico-chemical processes that explain their change in size spectra, specifically in relation to aerosols and CCN. Understanding organic aerosols and CCN in this context provides clear benefits to quantifying the role of marine nanogel/microgel in microphysical processes leading to cloud formation. This review emphasizes the DOC-marine gel/aerosolized gel-cloud link, critical to developing accurate climate models. 

Marine dissolved organic matter (DOM) holds ~660 billion metric tons of carbon, making it one of Earth’s major carbon reservoirs that is exchangeable with the atmosphere on annual to millennial time scales. The global ocean scale dynamics of the pool have become better illuminated over the past few decades, and those are very briefly described here. What is still far from understood is the dynamical control on this pool at the molecular level; in the case of this Special Issue, the role of microgels is poorly known. This manuscript provides the global context of a large pool of marine DOM upon which those missing insights can be built. 

About 20% of the organic carbon produced in the sunlit surface ocean is transported into the ocean’s interior as dissolved, suspended and sinking particles to be mineralized and sequestered as dissolved inorganic carbon (DIC), sedimentary particulate organic carbon (POC) or “refractory” dissolved organic carbon (rDOC). Recently, the physical and biological mechanisms associated with the particle pumps have been revisited, suggesting that accepted fluxes might be severely underestimated ( Boyd et al., 2019 ; Buesseler et al., 2020 ). Perhaps even more poorly understood are the mechanisms driving rDOC production and its potential accumulation in the ocean. On the basis of recent conflicting evidence about the relevance of DOC degradation in the deep ocean, we revisit the concept of rDOC in terms of its “refractory” nature in order to understand its role in the global carbon cycle. Here, we address the problem of various definitions and approaches used to characterize rDOC (such as turnover time in relation to the ocean transit time, molecule abundance, chemical composition and structure). We propose that rDOC should be operationally defined. However, we recognize there are multiple ways to operationally define rDOC; thus the main focus for unifying future studies should be to explicitly state how rDOC is being defined and the analytical window used for measuring rDOC, rather than adhering to a single operational definition. We also conclude, based on recent evidence, that the persistence of rDOC is fundamentally dependent on both intrinsic (chemical composition and structure, e.g., molecular properties), and extrinsic properties (amount or external factors, e.g., molecular concentrations, ecosystem properties). Finally, we suggest specific research questions aimed at stimulating research on the nature, dynamics, and role of rDOC in Carbon sequestration now and in future scenarios of climate change. 

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/m²and 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.