scholarly journals What Is Refractory Organic Matter in the Ocean?

2021 ◽  
Vol 8 ◽  
Author(s):  
Federico Baltar ◽  
Xosé A. Alvarez-Salgado ◽  
Javier Arístegui ◽  
Ronald Benner ◽  
Dennis A. Hansell ◽  
...  

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.

2013 ◽  
Vol 10 (9) ◽  
pp. 14861-14885 ◽  
Author(s):  
K. Schmidt ◽  
C. L. De La Rocha ◽  
M. Gallinari ◽  
G. Cortese

Abstract. Correlation between particulate organic carbon (POC) and calcium carbonate sinking through the deep ocean has led to the idea that ballast provided by calcium carbonate is important for the export of POC from the surface ocean. While this idea is certainly to some extent true, it is worth considering in more nuance, for example, examining the different effects on the aggregation and sinking of POC of small, non-sinking calcite particles like coccoliths and large, rapidly sinking calcite like planktonic foraminiferan tests. We have done that here in a simple experiment carried out in roller tanks that allow particles to sink continuously without being impeded by container walls. Coccoliths were efficiently incorporated into aggregates that formed during the experiment, increasing their sinking speed compared to similarly sized aggregates lacking added calcite ballast. The foraminiferan tests, which sank as fast as 700 m d−1, became associated with only very minor amounts of POC. In addition, when they collided with other, larger, foraminferan-less aggregates, they fragmented them into two smaller, more slowly sinking aggregates. While these effects were certainly exaggerated within the confines of the roller tanks, they clearly demonstrate that calcium carbonate ballast is not just calcium carbonate ballast- different forms of calcium carbonate ballast have notably different effects on POC aggregation, sinking, and export.


2014 ◽  
Vol 11 (1) ◽  
pp. 135-145 ◽  
Author(s):  
K. Schmidt ◽  
C. L. De La Rocha ◽  
M. Gallinari ◽  
G. Cortese

Abstract. Correlation between particulate organic carbon (POC) and calcium carbonate sinking through the deep ocean has led to the idea that ballast provided by calcium carbonate is important for the export of POC from the surface ocean. While this idea is certainly to some extent true, it is worth considering in more nuance, for example, examining the different effects on the aggregation and sinking of POC of small, non-sinking calcite particles like coccoliths and large, rapidly sinking calcite like planktonic foraminiferan tests. We have done that here in a simple experiment carried out in roller tanks that allow particles to sink continuously without being impeded by container walls. Coccoliths were efficiently incorporated into aggregates that formed during the experiment, increasing their sinking speed compared to similarly sized aggregates lacking added calcite ballast. The foraminiferan tests, which sank as fast as 700 m d−1, became associated with only very minor amounts of POC. In addition, when they collided with other, larger, foram-less aggregates, they fragmented them into two smaller, more slowly sinking aggregates. While these effects were certainly exaggerated within the confines of the rolling tanks, they clearly demonstrate that calcium carbonate ballast is not just calcium carbonate ballast – different forms of calcium carbonate ballast have notably different effects on POC aggregation, sinking, and export.


2020 ◽  
Vol 11 (1) ◽  
Author(s):  
S. M. Sosdian ◽  
T. L. Babila ◽  
R. Greenop ◽  
G. L. Foster ◽  
C. H. Lear

AbstractThe Miocene Climatic Optimum (MCO, 14–17 Ma) was ~3–4 °C warmer than present, similar to estimates for 2100. Coincident with the MCO is the Monterey positive carbon isotope (δ13C) excursion, with oceans more depleted in 12C relative to 13C than any time in the past 50 Myrs. The long-standing Monterey Hypothesis uses this excursion to invoke massive marine organic carbon burial and draw-down of atmospheric CO2 as a cause for the subsequent Miocene Climate Transition and Antarctic glaciation. However, this hypothesis cannot explain the multi-Myr lag between the δ13C excursion and global cooling. We use planktic foraminiferal B/Ca, δ11B, δ13C, and Mg/Ca to reconstruct surface ocean carbonate chemistry and temperature. We propose that the MCO was associated with elevated oceanic dissolved inorganic carbon caused by volcanic degassing, global warming, and sea-level rise. A key negative feedback of this warm climate was the organic carbon burial on drowned continental shelves.


Author(s):  
Sheng-Hsien Hsieh ◽  
Teng-Pao Chiu ◽  
Wei-Shiang Huang ◽  
Ting-Chien Chen ◽  
Yi-Lung Yeh

Soil humic substances (SHS) are heterogeneous, complex mixtures, whose concentration, chemical composition, and structure affect the transport and distribution of heavy metals. This study investigated the distribution behavior of two heavy metals [cadmium (Cd) and nickel (Ni)] in high molecular weight SHS (HMHS, 1 kDa–0.45 μm) and low molecular weight SHS (LMHS, <1 kDa) extracted from agricultural soils. The HMHS mass fractions were 45.1 ± 19.3%, 17.1 ± 6.7%, and 57.7 ± 18.5% for dissolved organic carbon (DOC), Cd, and Ni, respectively. The metal binding affinity, unit organic carbon binding with heavy metal ratios ([Me]/[DOC]), were between 0.41 ± 0.09 μmol/g-C and 7.29 ± 2.27 μmol/g-C. Cd preferred binding with LMHS (p < 0.001), while Ni preferred binding with HMHS (p < 0.001). The optical indicators SUVA254, SR, and FI were 3.16 ± 1.62 L/mg-C/m, 0.54 ± 0.18 and 1.57 ± 0.15, respectively for HMHS and 2.65 ± 1.25 L/mg-C/m, 0.40 ± 0.17, and 1.68 ± 0.12, respectively for LMHS. The HMHS contained more aromatic and lower FI values than LMHS. Multilinear regression showed a significant positive correlation between the measured predicted [Me]/[DOC] ratios (r = 0.52–0.72, p < 0.001). The results show that the optical indices can distinguish the chemical composition and structure of different size SHS and predict the binding ability of Me-SHS.


2016 ◽  
Vol 10 (4s) ◽  
pp. 595-600 ◽  
Author(s):  
Witold Brostow ◽  
◽  
Haley E. Hagg Lobland ◽  

The property of brittleness for polymers and polymer-based materials (PBMs) is an important factor in determining the potential uses of a material. Brittleness of polymers may also impact the ease and modes of polymer processing, thereby affecting economy of production. Brittleness of PBMs can be correlated with certain other properties and features of polymers; to name a few, connections to free volume, impact strength, and scratch recovery have been explored. A common thread among all such properties is their relationship to chemical composition and morphology. Through a survey of existing literature on polymer brittleness specifically combined with relevant reports that connect additional materials and properties to that of brittleness, it is possible to identify chemical features of PBMs that are connected with observable brittle behavior. Relations so identified between chemical composition and structure of PBMs and brittleness are described herein, advancing knowledge and improving the capacity to design new and to choose among existing polymers in order to obtain materials with particular property profiles.


2020 ◽  
pp. 34-39
Author(s):  
Aneta Antczak-Chrobot ◽  
Maciej Wojtczak

In this research paper, development of a procedure of isolation of exopolysaccharides from frost-damaged beet and an analysis of structural and chemical composition of polymers isolated from sugar beet of different origin are presented. Total acid hydrolysis degradation integrated with HPAEC-ED analysis has been utilized to confirm the monomeric composition of the separated polysaccharides. The implementation of NMR spectral analysis and SEC chromatography of the structure of exopolysaccharides has been investigated. The results demonstrate that the chemical composition and structure of exopolysaccharides depend on their origin. Typical exopolysaccharides from Central European beet roots consist mainly of glucose monomers – and they have low branched structure – about 90% of α-1,6 linkage which is typical for dextran. The exopolysaccharides isolated from Swedish beet are characterized by 50–60% fructose monomers. They contain only about 65% α-1,6 linkages. Exopolysaccharides extracted from various origin beet differ in average molecular mass. The molecular distribution is not normal.


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