Dissolved Black Carbon Concentrations Research Articles

Discharge of dissolved black carbon from a fire‐affected intertidal system

We report substantial tidal fluxes of dissolved black carbon (DBC) in a fire‐affected marsh in the northern Gulf of Mexico. DBC was molecularly determined as benzenepolycarboxylic acids in a tidal creek, adjacent rivers, and the coastal ocean. Supported by stable carbon isotope and in situ fluorescence measurements, three sources of dissolved organic carbon (DOC) were identified that mixed conservatively in the coastal system: groundwater from salt marshes, river water, and seawater. Groundwater was the main source of DBC to the creek. The highest DBC concentrations of up to 41 µmol C L−1 (7.2% of DOC) were found in the creek at low tide, compared with < 18 µmol C L−1 in all other samples. Over the studied tidal cycle, we determined a runoff (load per drainage area) of 3700 moles DBC (44 kg C) km−2 of salt marsh. This is high compared with the Apalachicola River, where the annual DBC runoff is on the order of 104 mol (120 kg C) km−2 yr−1. In the marsh, it would require ∼ 20 tidal cycles similar to the one that we studied to remove all black carbon produced during one fire event. Because a spring tide was studied, our estimate is as an upper limit. DBC is ubiquitous in the global ocean, and dissolution and subsequent lateral transport appear to be important removal mechanisms for soil black carbon. Our study, which provides a snapshot in time and space, demonstrates that tidal fluxes may be primary carriers of DBC, and therefore tidal pumping and groundwater discharge cannot be ignored in assessing the continental runoff of DBC.

Photo-lability of deep ocean dissolved black carbon

Abstract. Dissolved black carbon (DBC), defined here as condensed aromatics isolated from seawater via PPL solid phase extraction and quantified as benzenepolycarboxylic acid (BPCA) oxidation products, is a significant component of the oceanic dissolved organic carbon (DOC) pool. These condensed aromatics are widely distributed in the open ocean and appear to be tens of thousands of years old. As such DBC is regarded as highly refractory. In the current study, the photo-lability of DBC, DOC and coloured dissolved organic matter (CDOM; ultraviolet-visible absorbance) were determined over the course of a 28 day irradiation of North Atlantic Deep Water under a solar simulator. During the irradiation DBC fell from 1044 ± 164 nM-C to 55 ± 15 nM-C, a 20-fold decrease in concentration. Dissolved black carbon photo-degradation was more rapid and more extensive than for bulk CDOM and DOC. The concentration of DBC correlated with CDOM absorbance and the quality of DBC indicated by the ratios of different BPCAs correlated with CDOM absorbance spectral slope, suggesting the optical properties of CDOM may provide a proxy for both DBC concentrations and quality in natural waters. Further, the photo-lability of components of the DBC pool increased with their degree of aromatic condensation. These trends indicate that a continuum of compounds of varying photo-lability exists within the marine DOC pool. In this continuum, photo-lability scales with aromatic character, specifically the degree of condensation. Scaling the rapid photo-degradation of DBC to rates of DOC photo-mineralisation for the global ocean leads to an estimated photo-chemical half-life for oceanic DBC of less than 800 years. This is more than an order of magnitude shorter than the apparent age of DBC in the ocean. Consequently, photo-degradation is posited as the primary sink for oceanic DBC and the apparent survival of DBC molecules in the oceans for millennia appears to be facilitated not by their inherent inertness but by the rate at which they are cycled through the surface ocean's photic zone.