Oxygenation and organic-matter preservation in marine sediments: Direct experimental evidence from ancient organic carbon–rich deposits

Geology ◽  
2005 ◽  
Vol 33 (11) ◽  
pp. 889 ◽  
Author(s):  
Leon Moodley ◽  
Jack J. Middelburg ◽  
Peter M.J. Herman ◽  
Karline Soetaert ◽  
Gert J. de Lange
2021 ◽  
Vol 8 ◽  
Author(s):  
Emily M. Bristol ◽  
Craig T. Connolly ◽  
Thomas D. Lorenson ◽  
Bruce M. Richmond ◽  
Anastasia G. Ilgen ◽  
...  

Accelerating erosion of the Alaska Beaufort Sea coast is increasing inputs of organic matter from land to the Arctic Ocean, and improved estimates of organic matter stocks in eroding coastal permafrost are needed to assess their mobilization rates under contemporary conditions. We collected three permafrost cores (4.5–7.5 m long) along a geomorphic gradient near Drew Point, Alaska, where recent erosion rates average 17.2 m year−1. Down-core patterns indicate that organic-rich soils and lacustrine sediments (12–45% total organic carbon; TOC) in the active layer and upper permafrost accumulated during the Holocene. Deeper permafrost (below 3 m elevation) mainly consists of Late Pleistocene marine sediments with lower organic matter content (∼1% TOC), lower C:N ratios, and higher δ13C values. Radiocarbon-based estimates of organic carbon accumulation rates were 11.3 ± 3.6 g TOC m−2 year−1 during the Holocene and 0.5 ± 0.1 g TOC m−2 year−1 during the Late Pleistocene (12–38 kyr BP). Within relict marine sediments, porewater salinities increased with depth. Elevated salinity near sea level (∼20–37 in thawed samples) inhibited freezing despite year-round temperatures below 0°C. We used organic matter stock estimates from the cores in combination with remote sensing time-series data to estimate carbon fluxes for a 9 km stretch of coastline near Drew Point. Erosional fluxes of TOC averaged 1,369 kg C m−1 year−1 during the 21st century (2002–2018), nearly doubling the average flux of the previous half-century (1955–2002). Our estimate of the 21st century erosional TOC flux year−1 from this 9 km coastline (12,318 metric tons C year−1) is similar to the annual TOC flux from the Kuparuk River, which drains a 8,107 km2 area east of Drew Point and ranks as the third largest river on the North Slope of Alaska. Total nitrogen fluxes via coastal erosion at Drew Point were also quantified, and were similar to those from the Kuparuk River. This study emphasizes that coastal erosion represents a significant pathway for carbon and nitrogen trapped in permafrost to enter modern biogeochemical cycles, where it may fuel food webs and greenhouse gas emissions in the marine environment.


2020 ◽  
Author(s):  
Naiyu Zhang ◽  
Charlotte Thompson ◽  
Ian Townend

<p>In order to estimate sediment organic carbon budget in coastal oceans and continental shelves, a first step is to estimate how much of the deposited organic matter is retained within a sediment matrix, for further remineralization and preservation on a geological timescale, rather being physically flushed away by benthic flow<sup>1</sup>. This question becomes more challenging for the regions where ‘mobile’ layers (e.g. fluff layer, fluid mud and nepheloid layer) are formed due to the massive organic matter inputs, and often frequent resuspension and deposition<sup>2</sup>. Organic matter remineralization and preservation in sediments has been mostly investigated but often overlooks the role of flow-induced shear stresses on suspending the organic matter. While such flow influences in sediment organic matter budget may have little influence on sediment organic matter budget in deep oceans, it cannot be neglected in shallow-water coastal seas and continental shelves where cyclic resuspension, deposition and frequent storm events occur<sup>3,4</sup>. To our knowledge, the resistance strengths of organic matter in sediments against flow resuspension has received little attention.</p><p>To investigate this knowledge gap, various organo-clay aggregates and organo-clay-sand aggregates formed under different flow conditions were investigated by a series of laboratory flume<sup>5</sup> and high resolution X-ray Microcomputed Tomography (micro-CT) experiments<sup>6</sup>. Herein, a novel methodology is proposed, which successfully establishes quantitative relationships between the resuspension resistance strengths of these organic aggregates and a wide range of flow intensities, from moderate to storm conditions. The results provide a basis for computing resuspension under a range of flow conditions and, hence improving estimates of the organic matter budget in the coastal zone.  </p><p> </p><p><strong>References</strong></p><ol><li>Burdige, D. J. Preservation of organic matter in marine sediments: Controls, mechanisms, and an imbalance in sediment organic carbon budgets? Chem. Rev. <strong>107</strong>, 467–485 (2007).</li> <li>McKee, B. A., Aller, R. C., Allison, M. A., Bianchi, T. S. & Kineke, G. C. Transport and transformation of dissolved and particulate materials on continental margins influenced by major rivers: Benthic boundary layer and seabed processes. Cont. Shelf Res. (2004). doi:10.1016/j.csr.2004.02.009</li> <li>Burdige, D. J. Burial of terrestrial organic matter in marine sediments: A re-assessment. Global Biogeochem. Cycles <strong>19</strong>, 1–7 (2005).</li> <li>Nicholls, R. J. & Cazenave, A. Sea-level rise and its impact on coastal zones. Science (2010). doi:10.1126/science.1185782</li> <li>Thompson, C. E. L., Couceiro, F., Fones, G. R. & Amos, C. L. Shipboard measurements of sediment stability using a small annular flume-core mini flume (cmf). Limnol. Oceanogr. Methods (2013). doi:10.4319/lom.2013.11.604</li> <li>Zhang, N. et al. Nondestructive 3D Imaging and Quantification of Hydrated Biofilm-Sediment Aggregates Using X-ray Microcomputed Tomography. Environ. Sci. Technol. <strong>52</strong>, 13306–13313 (2018).</li> </ol>


1976 ◽  
Vol 33 (1) ◽  
pp. 93-97 ◽  
Author(s):  
Roger Pocklington

Marine sediments containing land-derived organic matter can be identified by a combination of high organic carbon concentration, high C and H relative to N, and the presence of lignin. Sediments with this combination of characteristics have been found in certain environments within the Gulf of St. Lawrence, in particular, in close proximity to pulp and paper mills.


Author(s):  
Donald Eugene Canfield

This chapter considers the aftermath of the great oxidation event (GOE). It suggests that there was a substantial rise in oxygen defining the GOE, which may, in turn have led to the Lomagundi isotope excursion, which was associated with high rates of organic matter burial and perhaps even higher concentrations of oxygen. This excursion was soon followed by a crash in oxygen to very low levels and a return to banded iron formation deposition. When the massive amounts of organic carbon buried during the excursion were brought into the weathering environment, they would have represented a huge oxygen sink, drawing down levels of atmospheric oxygen. There appeared to be a veritable seesaw in oxygen concentrations, apparently triggered initially by the GOE. The GOE did not produce enough oxygen to oxygenate the oceans. Dissolved iron was removed from the oceans not by reaction with oxygen but rather by reaction with sulfide. Thus, the deep oceans remained anoxic and became rich in sulfide, instead of becoming well oxygenated.


Author(s):  
Jeonghyun Kim ◽  
Yeseul Kim ◽  
Sung Eun Park ◽  
Tae-Hoon Kim ◽  
Bong-Guk Kim ◽  
...  

AbstractIn Jeju Island, multiple land-based aquafarms were fully operational along most coastal region. However, the effect of effluent on distribution and behaviours of dissolved organic matter (DOM) in the coastal water are still unknown. To decipher characteristics of organic pollution, we compared physicochemical parameters with spectral optical properties near the coastal aquafarms in Jeju Island. Absorption spectra were measured to calculate the absorption coefficient, spectral slope coefficient, and specific UV absorbance. Fluorescent DOM was analysed using fluorescence spectroscopy coupled with parallel factor analysis. Dissolved organic carbon (DOC) and total dissolved nitrogen (TDN) were measured using high-temperature catalytic oxidation. The DOC concentration near the discharge outlet was twice higher than that in natural groundwater, and the TDN concentration exponentially increased close to the outlet. These distribution patterns indicate that aquafarms are a significant source of DOM. Herein, principal component analysis was applied to categorise the DOM origins. There were two distinct groups, namely, aquaculture activity for TDN with humic-like and high molecular weights DOM (PC1: 48.1%) and natural biological activity in the coastal water for DOC enrichment and protein-like DOM (PC2: 18.8%). We conclude that the aquafarms significantly discharge organic nitrogen pollutants and provoke in situ production of organic carbon. Furthermore, these findings indicate the potential of optical techniques for the efficient monitoring of anthropogenic organic pollutants from aquafarms worldwide.


2021 ◽  
Author(s):  
Marttiina V. Rantala ◽  
Carsten Meyer-Jacob ◽  
E. Henriikka Kivilä ◽  
Tomi P. Luoto ◽  
Antti. E. K. Ojala ◽  
...  

AbstractGlobal environmental change alters the production, terrestrial export, and photodegradation of organic carbon in northern lakes. Sedimentary biogeochemical records can provide a unique means to understand the nature of these changes over long time scales, where observational data fall short. We deployed in situ experiments on two shallow subarctic lakes with contrasting light regimes; a clear tundra lake and a dark woodland lake, to first investigate the photochemical transformation of carbon and nitrogen elemental (C/N ratio) and isotope (δ13C, δ15N) composition in lake water particulate organic matter (POM) for downcore inferences. We then explored elemental, isotopic, and spectral (inferred lake water total organic carbon [TOC] and sediment chlorophyll a [CHLa]) fingerprints in the lake sediments to trace changes in aquatic production, terrestrial inputs and photodegradation before and after profound human impacts on the global carbon cycle prompted by industrialization. POM pool in both lakes displayed tentative evidence of UV photoreactivity, reflected as increasing δ13C and decreasing C/N values. Through time, the tundra lake sediments traced subtle shifts in primary production, while the woodland lake carried signals of changing terrestrial contributions, indicating shifts in terrestrial carbon export but possibly also photodegradation rates. Under global human impact, both lakes irrespective of their distinct carbon regimes displayed evidence of increased productivity but no conspicuous signs of increased terrestrial influence. Overall, sediment biogeochemistry can integrate a wealth of information on carbon regulation in northern lakes, while our results also point to the importance of considering the entire spectrum of photobiogeochemical fingerprints in sedimentary studies.


2021 ◽  
Vol 770 ◽  
pp. 145307
Author(s):  
Mohammad Bahadori ◽  
Chengrong Chen ◽  
Stephen Lewis ◽  
Sue Boyd ◽  
Mehran Rezaei Rashti ◽  
...  

2020 ◽  
Vol 55 (2) ◽  
pp. 184-197
Author(s):  
Saeideh Mirzaei ◽  
Beata Gorczyca

Abstract In this study, diffused aeration was applied to remove trihalomethane (THM) compounds from chlorinated, treated water containing high dissolved organic carbon (DOC) of 6.8 ± 1.2 mg/L. Increasing air-to-water volumetric ratio (rA/W) from 16 to 39 enhanced total THM (TTHM) removal from 60 to 70% at 20 °C and from 30 to 50% at 4 °C. Although bromodichloromethane has lower Henry's law constant than chloroform (CF), it was removed by a higher degree than CF in some aeration trials. Albeit obtaining high removals in aeration, TTHM reformed, and their concentration surpassed the Canadian guideline of 100 ppb in about 24 hours at 20 °C and 40 hours at 10 °C in all attempted air-to-water ratios. The water age in the system investigated in this study varied from 48 hours in midpoint chlorine boosting stations to 336 hours in the nearest endpoint. This study showed that THM removal by aeration is not a viable solution to control the concentration of these disinfection by-products in high-DOC treated water and in distribution systems where water age exceeds 24 hours; unless, it is going to be installed at the distribution endpoints.


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