Burial Efficiency Research Articles

Carbon, iron and sulphur cycling in the sediments of a Mediterranean lagoon (Ghar El Melh, Tunisia)

Coastal lagoon sediments are important for the biogeochemical carbon cycle at the land-ocean transition, as they form hotspots for organic carbon burial, as well as potential sites for authigenic carbonate formation. Here, we employ an early diagenetic model to quantify the coupled redox cycling of carbon, iron and sulphur in the sediments of the shallow Ghar El Melh (GEM) lagoon (Tunisia). The model simulated depth profiles show a good correspondence with available pore water data (dissolved inorganic carbon, NH4+, total alkalinity, Ca2+, Fe2+ and SO42−) and solid phase data (organic matter, pyrite, calcium carbonate and iron (oxyhydr)oxides). This indicates that the model is able to capture the dominant processes influencing the sedimentary biogeochemical cycling. Our results show that sediment of the GEM lagoon is an efficient reactor for organic matter breakdown (burial efficiency < 10%), with an important role for aerobic respiration (32%) and sulphate reduction (61%). Despite high rates of sulphate reduction, free sulphide does not accumulate in the pore water, due to a large terrestrial input of reactive iron oxides and the efficient sequestration of free sulphide into iron sulphide phases. High pyrite burial (2.2 mmol FeS2 m−2 d−1) prevents the reoxidation of reduced sulphide, thus resulting in a low total oxygen uptake (4.7 mmol m−2 d−1) of the sediment and a relatively high oxygen penetration depth. The formation of pyrite also generates high amounts of alkalinity in the pore water, which stimulates authigenic carbonate precipitation (2.7 mmol m−2 d−1) and leads to alkalinity release to the overlying water (3.4 mmol m−2 d−1). Model simulations with and without an N-cycle reveal a limited influence of nitrification and denitrification on overall organic matter diagenesis. Overall, our study highlights the potential role of coastal lagoons for the global carbon and sulphur cycle, and their possible contribution to shelf alkalinity, which increases the buffering capacity of the coastal ocean for CO2 uptake.

Reduced Mineralization of Terrestrial OC in Anoxic Sediment Suggests Enhanced Burial Efficiency in Reservoirs Compared to Other Depositional Environments.

Freshwater reservoirs are important sites of organic carbon (OC) burial, but the extent to which reservoir OC burial is a new anthropogenic carbon sink is currently unclear. While burial of aquatic OC (by, e.g., phytoplankton) in reservoirs may count as a new C sink, the burial of terrestrial OC in reservoirs constitutes a new C sink only if the burial is more efficient in reservoirs than in other depositional environments. We carried out incubation experiments that mimicked the environmental conditions of different depositional environments along the land‐sea continuum (oxic and anoxic freshwater, oxic and anoxic seawater, oxic river bedload, and atmosphere‐exposed floodplain) to investigate whether reservoirs bury OC more efficiently compared to other depositional environments. For sediment OC predominantly of terrestrial origin, OC degradation rates were significantly lower, by a factor of 2, at anoxic freshwater and saltwater conditions compared to oxic freshwater and saltwater, river, and floodplain conditions. However, the transformation of predominantly terrestrial OC to methane was one order of magnitude higher in anoxic freshwater than at other conditions. For sediment OC predominantly of aquatic origin, OC degradation rates were uniformly high at all conditions, implying equally low burial efficiency of aquatic OC (76% C loss in 57 days). Since anoxia is more common in reservoirs than in the coastal ocean, these results suggest that reservoirs are a depositional environment in which terrestrial OC is prone to become buried at higher efficiency than in the ocean but where also the terrestrial OC most efficiently is transformed to methane.

Enhanced mineralization of sedimentary organic carbon induced by excess carbon from phytoplankton in a eutrophic plateau lake

Large additions of organic carbon (OC) have been introduced into the carbon cycle of lakes from algae during the process of lake eutrophication. The impact of eutrophication on OC burial and CO2 fixing has been widely studied; however, there is still a gap regarding the impact of excess OC from algae on sedimentary OC mineralization. In this study, we aim to fill this gap by analyzing in situ measurements. Three pairs of sediment cores collected from a plateau lake (Dianchi Lake) in 2006 and 2014 were used to estimate the accumulation loss rate (ALR) of OC (and thus the total mineralization rate) in the sediment. n-Alkanes, measured from the same sedimentary cores, were used to identify the source of OC. An OC mineralization experiment in a laboratory was used to confirm the enhanced effect of excess phytoplankton carbon on ALR and reveal the potential influence of microorganisms. The results indicate that the sedimentary core (core 3), with high excess OC from algae (located in an algal bloom area), possessed a higher ALR (85.66%) and a higher attenuation coefficient (0.078), indicating the low burial efficiency and short mineralization duration of OC. Sedimentary core 1, controlled by terrestrial OC, had a relatively lower ALR (64.60%) and lower attenuation coefficient (0.029), indicating a high burial efficiency and long period of OC mineralization. The mineralization of OC in core 2 was impacted by terrestrial and endogenous OC, with an ALR of 72.00% and attenuation coefficient of 0.064, which is between that of cores 1 and 3. Excess OC from algae corresponded to an increase in ALR by 32.60% when comparing core 1 to core 3. The increased ALR and attenuation coefficient could be caused by excess OC from algae. Sedimentary OC mineralization indicates that the ALR with dominantly allochthonous OC (64.60%) is much lower than that controlled by autochthonous OC (85.66%). Excess OC from phytoplankton increases the mineralization of OC: not only via increased ALR but also increased mineralization speed. The laboratory experiment on the mixture of algae and sediment suggested that excess phytoplankton OC increased the emission of CO2 by 20–70% (mineralization rate).

Temporal constraints on lateral organic matter transport along a coastal mud belt

Constraints on timescales of lateral transport of sedimentary organic carbon (OC) over continental shelves and associated influences on the distribution and abundance of OC remain sparse. Preferential degradation of labile, young OC during lateral transport results in apparent “diagenetic aging” of OC. Additionally, sediment translocation can also result in “transport time-associated aging” of associated organic matter (OM) as a function of the lateral transport time (LTT). Here, we use a coupled thermal decomposition and radiocarbon (14C) approach to constrain timescales of lateral transport and concomitant loss of OC associated with different grain size fractions of sediments collected from two locations ∼275 km apart along a dispersal pathway on the inner shelf of the East China Sea. The 14C age contrasts between corresponding thermal fractions are used to distinguish these two components of sedimentary OM “aging”. To minimize interferences from hydrodynamic sorting and diagenetic aging of OC accompanying lateral transport, we assess 14C age differences of decomposition products from the most thermally-refractory OC components associated with specific grain size fractions between locations. We show that LTTs vary among different grain size fractions, and examine relationships between LTTs and sedimentary OC loss in order to assess the decomposition of OC as a consequence of lateral transport. We suggest that the decomposition of OC associated with protracted lateral transport exerts a strong influence on OC burial efficiency, with broad implications for carbon cycling over continental shelves.

Dissolved silica in the subterranean estuary and the impact of submarine groundwater discharge on the global marine silica budget

Groundwater's role in the global marine budget of dissolved silica (DSi), an essential nutrient, is constrained using DSi groundwater concentrations from multiple endmember lithologies and a global terrestrial submarine groundwater discharge (SGD) model. We report new DSi concentrations in nine subterranean estuaries throughout the world, including Panama, Mauritius, Guam, Yucatan (Mexico), Chile, Argentina, Southwest Florida (USA), Long Island Sound (USA) and Waquoit Bay (USA). These new data are augmented with a literature survey of DSi endmember concentrations in the subterranean estuary to determine the global DSi endmember in SGD, classified by the regional lithology (carbonate, shale, sandstone, extrusive igneous, shield and “complex”). DSi fluxes to the ocean from terrestrial (fresh) SGD equal 0.7 ± 0.1 Tmol y−1, more than half of which enters the Pacific Ocean. Non-conservative DSi enrichment was observed in marine groundwaters circulated through extrusive igneous and complex lithology sediments for twenty different study sites. Dissolution rate calculations indicate that non-conservative DSi enrichments in marine groundwaters can be supported, in part, by lithogenic dissolution of the coastal sediment, rather than biogenic silica dissolution. We make preliminary estimates of DSi inputs via marine SGD in shallow coastal aquifers of ~3 Tmol y−1. Considering recent revisions to the marine silica budget (e.g., increased estimates of biogenic silica storage via reverse weathering reactions, increased estimates of standing stocks of biogenic silica, and changing estimates of silica burial efficiency), sources and sinks in the marine Si budget can be balanced when taking into account estimates of new DSi inputs from total SGD (terrestrial and marine flow paths). These findings impact the residence time of oceanic Si and mass balances of the stable Si isotopes, as well as associated silicate weathering products, including Li and Ge.

Organic carbon recycling in Baltic Sea sediments – An integrated estimate on the system scale based on in situ measurements

In situ measured benthic fluxes of dissolved inorganic carbon (DIC), a proxy for organic carbon (OC) oxidation or recycling rates, are used together with burial rates based on measured sediment accumulation rates (SAR) and vertical distribution of OC in the sediment solid phase to construct a benthic OC budget for the Baltic Sea system. The large variability in recycling rates (4.3 ± 0.87–33 ± 17 mmol C m−2 d−1) and burial rates (1.2 ± 0.8–5.9 ± 1.8 mmol C m−2 d−1) between different sub-basins and between different depositional areas within the basins is accounted for in the budget. Our results indicate that sediments in the Baltic Sea have much higher recycling rates and lower burial rates of OC than previously found. The sediment budget calculations show that 22 ± 7.8 Tg C yr−1 of OC is recycled to the water column due to organic matter oxidation, while long term burial amounts to 1.0 ± 0.3 Tg C yr−1. For the Baltic Sea as a whole, 96% of the particulate OC (POC) deposited on the sea floor (23 ± 7.8 Tg C yr−1; the sum of recycling and burial) is recycled back to the water column. However, the burial efficiency (i.e. the fraction buried of the total deposition) shows large variability between the different basins (2.5–16%). The total benthic POC deposition is approximately 20% higher than the estimated POC source originating from primary production in the water column and riverine input. This difference is likely within the uncertainty range of our budget calculations, however it indicates that the POC sources might be underestimated. The results from this study enhance the understanding of OC delivery, deposition and cycling in the Baltic Sea, and help improving existing Baltic OC budgets.

Quantifying Phosphorus Sources and Sinks in the Gaoping River-Sea System in Southwestern Taiwan

This study aims to quantify sources and sinks of phosphorus (P) in the small mountainous river (SMR)-sea system in southwestern Taiwan. The Gaoping River (GP) exported total phosphorus (TP) at 1.08 × 109 mol year−1 into the GP coastal sea, corresponding to a global highest TP yield of 3.28 × 105 mol km−2 year−1 from the watershed during the study period. The river water TP comprised of 98.2% particulate P (PP) and 1.8% dissolved P. The PP was associated mainly with 10–63 μm particles and comprised 92.5% particulate inorganic P (PIP) and 7.5% particulate organic P (POP). The river flux of TP (or TP yield) was primarily determined by the sediment load which in turn was driven by river discharge varying with local climate variability. In the GP coastal sea, sedimentation rates decreased gradually with water depth, ranging from 0.032 to 1.62 g cm−2 year−1, and the highest rates were located on both sides of the GP Canyon, likely the result of typhoon impacts. The burial fluxes of the PP ranged from 0.02 to 0.84 mg cm−2 year−1, comprising approximately 88% PIP and 12% POP. The total deposition rates of sediment and PP were approximately 6.6 × 106 t year−1 and 4227 t year−1, respectively, in the study area, if integrated over an area of 3045 km2, with a maximum water depth of 1500 m. The burial efficiency of PP in the GP coastal sea ranged from 44 to 95%, which decreased generally with sampling location depth. A budget model showed that the imbalance of P sources (1.08 × 109 mol P year−1) and sinks (1.36 × 108 mol P year−1) implies about 90% of river inputs being recycled or exported out of the study area. The SMR margin that is associated with the canyon may act as an efficient conduit in transporting TP across the narrow margin into deep oceans.

Formation and preservation of authigenic pyrite in the methane dominated environment

Sulfate reduction could go through dissimilatory sulfate reduction and anaerobic methane oxidation couple with sulfate reduction (AOM-SR) with pyrite the end product. While AOM-SR is an important process in oxidizing methane and limiting methane entering the ocean, there is limited information available regarding pyrite formation and preservation under methane dominated environment. The purpose of this study is to report pyrite formation and preservation at a methane dominated environment, the YuanAn Ridge, where methane seeps have been observed, and to evaluate how would that differ from typical anoxic environment. Pore water methane, sulfate, dissolved sulfide, barium, and sediment pyrite, barium/Al ratio and organic carbon in sediments were analyzed from sediments collected by piston cores on board the R/V Ocean Researcher I (OR-I) from the study environment.The results showed methane flux is controlling pyrite formation in this methane dominated environment. Pyrite concentration is linearly correlated with methane flux with exceptions to shallower sulfate methane transition zone (SMTZ) sites where methane could have vent directly to the overlying water and contribute less to the pyrite formation. The more methane entering the SMTZ, the more pyrite formed and preserved in the sulfate methane transition zone sediments. Authigenic pyrite from dissimilatory sulfate reduction is a small fraction of the pyrite found in the methane dominant and low in organic carbon environment, with majority of pyrite derived from AOM-SR.Large spatial variations on rate of sulfate reduction, pyrite and methane concentrations were observed in the studied area sediments. Depth of sulfate methane transition zone varied between 1 and 14 m and is a log function of methane flux. Pore water sulfate profiles displayed three different types, linear, concave up and down, indicating methane flux have varied in time.Pyrite burial efficiency is high, approximately 50% of sulfate entering the SMTZ were preserved in sediments as pyrite. This efficiency of sulfate reduction through AOM-SR is much higher than pyrite formation from dissimilatory sulfate reduction in normal marine sediments. The AOM-SR and pyrite formation occurred at depth within the SMTZ favor a higher degree of pyrite preservation. Time require for the pyrite formation is about 4400 years in the YAR sediments, based on diffusion model calculation of barium sulfate precipitation.

A new look at the multi-G model for organic carbon degradation in surface marine sediments for coupled benthic–pelagic simulations of the global ocean

Abstract. The kinetics of particulate organic carbon (POC) mineralization in marine surface sediments is not well constrained. This creates considerable uncertainties when benthic processes are considered in global biogeochemical or Earth system circulation models to simulate climate–ocean interactions and biogeochemical tracer distributions in the ocean. In an attempt to improve our understanding of the rate and depth distribution of organic carbon mineralization in bioturbated (0–20 cm) sediments at the global scale, we parameterized a 1-D diagenetic model that simulates the mineralization of three discrete POC pools (a multi-G model). The rate constants of the three reactive classes (highly reactive, reactive, refractory) are fixed and determined to be 70, 0.5 and ∼ 0.001 yr−1, respectively, based on the Martin curve model for pelagic POC degradation. In contrast to previous approaches, however, the reactivity of the organic material degraded in the seafloor is continuous with, and set by, the apparent reactivity of material sinking through the water column. Despite the simplifications of describing POC remineralization using G-type approaches, the model is able to simulate a global database (185 stations) of benthic oxygen and nitrate fluxes across the sediment–water interface in addition to porewater oxygen and nitrate distributions and organic carbon burial efficiencies. It is further consistent with degradation experiments using fresh phytoplankton reported in a previous study. We propose that an important yet mostly overlooked consideration in upscaling approaches is the proportion of the reactive POC classes reaching the seafloor in addition to their reactivity. The approach presented is applicable to both steady-state and non-steady state scenarios, and links POC degradation kinetics in sedimentary environments to water depth and the POC rain rate to the seafloor.

Effect of sea-level on organic carbon preservation in the Okinawa Trough over the last 91 kyr

The burial of marine organic carbon, primarily synthesized by marine autotrophic organisms, into sediment removes CO2 from the ocean-atmosphere system. However, linkages between export productivity and organic carbon burial and the controlling factors remained ambiguous, especially for marginal seas. In this study, we measured redox-sensitive trace metal concentrations and planktic foraminifer fauna assemblages for a sediment core collected from the middle Okinawa Trough spanning the past 91 kyr. Through compilation with other published data, we found that the export productivity was decoupled from organic carbon burial. Variability of manganese and total sulfur contents suggested that both bottom water and surface sediment had experienced significant redox change in the last glacial cycle. By using the ratio of marine organic carbon to reactive phosphorus, i.e., OCmarine/Preact., we reconstructed organic carbon burial efficiency which showed relatively higher values during the last glacial and low values during the middle-late Holocene. After synthesizing our new and reported data, we conclude that the middle Okinawa Trough bottom water redox state was controlled by deep water ventilation induced by sea level change and related Kuroshio Current intrusion, instead of by the oxygen consumption owing to local export productivity.

Bioturbation and directionality in Earth's carbon isotope record across the Neoproterozoic–Cambrian transition

Mixing of sediments by moving animals becomes apparent in the trace fossil record from about 550 million years ago (Ma), loosely overlapping with the tail end of the extreme carbonate carbon isotope δ13 Ccarbonate fluctuations that qualitatively distinguish the Proterozoic geochemical record from that of the Phanerozoic. These Precambrian-scale fluctuations in δ13 Ccarbonate (PSF-δ13 Ccarbonate ) remain enigmatic, due to their high amplitude and inclusion of global-scale negative δ13 Ccarbonate values, below anything attributable to mantle input. Here, we note that different biogeochemical-model scenarios plausibly explaining globally synchronous PSF-δ13 Ccarbonate converge: via mechanistic requirements for extensive anoxia in marine sediments to support sedimentary build-up of 13 C-depleted carbon. We hypothesize that bioturbation qualitatively reduced marine sediment anoxia by exposing sediments to oxygenated overlying waters, which ultimately contributed to decreasing the carbon cycle's subsequent susceptibility to PSF- δ13 Ccarbonate . Bioturbation may also have reduced the quantity of (isotopically light) organic-derived carbon available to contribute to PSF- δ13 Ccarbonate via ocean crust carbonatization at depth. We conduct a comparative modelling exercise in which we introduce bioturbation to existing model scenarios for PSF- δ13 Ccarbonate : expressing both the anoxic proportion of marine sediments, and the global organic carbon burial efficiency, as a decreasing function of bioturbation. We find that bioturbation's oxygenating impact on sediments has the capacity to prevent PSF- δ13 Ccarbonate caused by authigenic carbonate precipitation or methanogenesis. Bioturbation's impact on the f-ratio via remineralization is partially offset by liberation of organic phosphate, some of which feeds back into new production. We emphasize that this study is semiquantitative, exploratory and intended merely to provide a qualitative theoretical framework within which bioturbation's impact on long-term, first-order δ13 Ccarbonate can be assessed (and it is hoped quantified in more detail by future work). With this proviso, we conclude that it is entirely plausible that bioturbation made a decisive contribution to the enigmatic directionality in the δ13 Ccarbonate record, from the Neoproterozoic-Cambrian boundary onwards.

Sources, distributions, and burial efficiency of terrigenous organic matter in surface sediments from the Yellow River mouth, northeast China

Organic geochemical studies of surface sediments from Laizhou Bay, the Yellow River mouth, northeast China, were conducted to reveal the sources, distributions, and burial efficiency of terrigenous OC exported by the Yellow River. Bulk OC contents and δ13Corg values from 204 samples show that terrigenous OC mainly accumulates in two muddy patches, basically controlled by hydrodynamic conditions. Distributions and stable carbon isotopic compositions of individual n-alkanes from 45 samples suggest that short-chain n-alkanes, with even carbon-number predominance, are most likely microbial products from degradation of riverine fossil OC, whereas long-chain odd-numbered n-alkanes (n-C27, n-C29 and n-C31) and long-chain even-numbered n-alkanes (n-C26,n-C28 and n-C30) are representative of riverine soil OC and fossil OC, respectively. Integrated with previous reports of ∼100% burial efficiency of soil OC in the Yellow River mouth, concentration ratios of n-C27+29+31 to OC and n-C26+28+30 to n-C27+29+31 from the riverine particles to surface sediments in Laizhou Bay were constructed to indicate relative terrigenous OC contributions and fossil OC burial efficiency, respectively. The results suggest that the terrigenous OC contribution ranges from 14% to 57% in Laizhou Bay, with the highest values in the two muddy patches as well as in areas near the river mouth. The fossil OC burial efficiency ranges from 36% to 76%, with an TOC-weighted mean value of 42%. The 58% fossil OC lost during the transport and burial processes in the Yellow River mouth may provide a significant CO2 source.

Benthic cycling of phosphorus in the Eastern Arabian Sea: Evidence of present day phosphogenesis

Abstract Results of a study on phosphorus (P) cycling in the Eastern Arabian Sea provides convincing evidence of present-day phosphogenesis in the study area. This finding contrasts with previous reports of the occurrence of only old phosphorites along the Indian margin. Extensive benthic P regeneration is observed in the sediments that are deposited on topographic highs in the western Indian continental margin , which is impinged by a perennial oxygen minimum zone (OMZ). The phosphate flux from the sediments ranged between 1.1 and 22 mmol m− 2 yr− 1. Among the P reservoirs, biogenic P (Pbio) is the major pool of P within the upper 30 cm of sediment. P released from organic matter decomposition and fish debris dissolution mainly controls benthic P regeneration while the role of redox cycling of iron is weak. The change in authigenic P (Pauth ) with depth in the sediment and concomitant decrease in porewater dissolved inorganic phosphate (DIP), solid phase P bio and organic P (Porg) content collectively indicate the transformation of P from labile phases to an authigenic phase. Molar Corg/Porg and Corg/Preactive ratios also support the notion of ongoing phosphogenesis in the area. The content of carbonate fluroapatite (CFA) is elevated especially in one of the three study sites as a result of in-situ precipitation and a contribution from eolian and water column authigenesis . The estimated burial efficiency of P at the sediment-water interface at two locations is only about 2%, which is much less than in the western Arabian Sea also indicating extensive P regeneration.

Sources and radiocarbon ages of aerosol organic carbon along the east coast of China and implications for atmospheric fossil carbon contributions to China marginal seas

Aerosol deposition is an important mechanism for the delivery of terrestrial organic carbon (OC) to marginal seas, but OC age characteristics of aerosols are not well constrained and their contributions to sediment OC burial have not been quantified. Total suspended particle samples were collected along the east coast of China at Changdao (CD), Qingdao (QD) and Huaniao Island (HNI), and were analyzed for total organic carbon (TOC) isotopes (13C and 14C) in order to bridge this information gap. TOC δ13C and Δ14C values ranged from −23.6 to −30.5‰, and −153 to −687‰, respectively, with the latter corresponding to 14C ages ranging from 1280 to 9260yr. Estimated contributions of fossil carbon to TOC based on 14C mass balance approach ranged from 26 to 73%, with strong seasonal variations in fossil carbon observed at CD. Fossil carbon at CD showed the highest proportion (73%) in winter, reflecting anthropogenic emissions and the lowest proportion (26%) in summer, caused by biomass contribution (annual ave., 52%±17%). In contrast, the fossil carbon at both QD (57–64%) and HNI (57–67%) dominated throughout the year, reflecting local anthropogenic influences and long-range transport. Mass balance estimates indicate that atmospheric deposition and riverine export accounted for 31% and 69% of fossil carbon inputs to the China marginal seas (CMS) respectively, with fossil carbon burial efficiencies approaching 100% in the CMS. On a global scale, an atmospheric fossil carbon deposition flux of 17.2TgCyr−1 was estimated, equivalent to 40% of the estimated fluvial flux to the ocean, and potentially accounting for 24–41% of fossil OC burial in marine sediments. Therefore, the atmospheric deposition constitutes an important source of fossil carbon to marine sediments, and could play a key role in regional and global scale OC budgets and biogeochemical cycles.

Phosphorus dynamics in and below the redoxcline in the Black Sea and implications for phosphorus burial

Marine basins with oxygen-depleted deep waters provide a natural laboratory to investigate the consequences of anoxic and sulfidic (i.e. euxinic) conditions for biogeochemical processes in seawater and sediments. In this study, we investigate the dynamics of the key nutrient phosphorus (P) and associated elements such as manganese (Mn), iron (Fe) and calcium (Ca) in the euxinic deep basin of the Black Sea. By examining water column particles with scanning electron microscope – energy dispersive spectroscopy and synchrotron-based X-ray absorption spectroscopy, we show that Mn(III/IV)-P is the key form of particulate P in the redoxcline. Other forms of particulate P include organic P, Fe(III)-P, and inorganic polyphosphates. Most inorganic P particles that are formed in the redoxcline subsequently dissolve in the underlying sulfidic waters, with the exception of some particulate Fe(III)-P that accounts for <1% of all P settling onto the seafloor. Organic P is the dominant source of P to the sediment. Most of this organic P is degraded in the upper 2 cm of the sediment. Results of sequential extractions and a 33P radiotracer experiment point towards the formation of labile Ca-P and P adsorbed onto calcium-carbonate and clays and a role of these phases as a major sink of P in the sediment. The total P burial efficiency in the sediments is ∼27%, which is relatively high when compared to estimates for sediments in other euxinic basins such as the Baltic Sea (<12%). We suggest that the abundant presence of calcium carbonate may contribute to the more efficient sequestration of P in Black Sea sediments.

Carbon and nitrogen burial in a plateau lake during eutrophication and phytoplankton blooms

Organic carbon (OC) buried in lake sediment is an important component of the global carbon cycle. The impact of eutrophication on OC burial in lakes should be addressed due to worldwide lake eutrophication. Fourteen 210Pb- and 137Cs-dated sediment cores taken in Dianchi Lake (China) in August 2006 (seven cores) and July 2014 (seven cores) were analyzed to evaluate the response of the organic carbon accumulation rate (OCAR) to eutrophication and algal blooms over the past hundred years. The mean value of OCAR before eutrophication occurred in 1979, 16.62±7.53 (mean value±standard deviation), increased to 54.33±27.29gm−2yr−1 after eutrophication. It further increased to 61.98±28.94gm−2yr−1 after algal blooms occurred (1989). The accumulation rate of organic nitrogen (ONAR) is coupled with OCAR. The high loss rate of OC and organic nitrogen (ON) leads to a long-term burial efficiency of only 10% and 5% of OC and ON. However, this efficiency can still lead to an increase in OCAR by a factor of 4.55 during algal blooms in Dianchi Lake. Dianchi Lake stored 1.26±0.32 Tg carbon and 0.071±0.018 Tg nitrogen, including 0.94±0.23 Tg OC and 0.32±0.14 Tg inorganic carbon, 0.066±0.018 Tg ON, 0.002±0.001 Tg nitrate nitrogen (NO3-N) and 0.003±0.001 Tg ammonium nitrogen (NH4-N) between 1900 and 2012.

Temperature Dependence of Apparent Respiratory Quotients and Oxygen Penetration Depth in Contrasting Lake Sediments

AbstractLake sediments constitute an important compartment in the carbon cycle of lakes, by burying carbon over geological timescales and by production and emission of greenhouse gases. The degradation of organic carbon (OC) in lake sediments is linked to both temperature and oxygen (O2), but the interactive nature of this regulation has not been studied in lake sediments in a quantitative way. We present the first systematic investigation of the effects of temperature on the apparent respiratory quotient (RQ, i.e., the molar ratio between carbon dioxide (CO2) production and O2 consumption) in two contrasting lake sediments. Laboratory incubations of sediment cores of a humic lake and an eutrophic lake across a 1–21°C temperature gradient over 157 days revealed that both CO2 production and O2 consumption were positively, exponentially, and similarly dependent on temperature. The apparent RQ differed significantly between the lake sediments (0.63 ± 0.26 and 0.99 ± 0.28 in the humic and the eutrophic lake, respectively; mean ± SD) and was significantly and positively related to temperature. The O2 penetration depth into the sediment varied by a factor of 2 over the 1–21°C temperature range and was significantly, negatively, and similarly related to temperature in both lake sediments. Accordingly, increasing temperature may influence the overall extent of OC degradation in lake sediments by limiting O2 supply to aerobic microbial respiration to the topmost sediment layer, resulting in a concomitant shift to less effective anaerobic degradation pathways. This suggests that temperature may represent a key controlling factor of the OC burial efficiency in lake sediments.

Phosphorus Cycling and Burial in Sediments of a Seasonally Hypoxic Marine Basin

Recycling of phosphorus (P) from sediments contributes to the development of bottom-water hypoxia in many coastal systems. Here, we present results of a year-long assessment of P dynamics in sediments of a seasonally hypoxic coastal marine basin (Lake Grevelingen, the Netherlands) in 2012. Sequential phosphorus extractions (SEDEX) and X-ray absorption spectroscopy (XAS) indicate that P was adsorbed to Fe-(III)-(oxyhydr)oxides when cable bacteria were active in the surface sediments in spring. With the onset of summer hypoxia, sulphide-induced dissolution of the Fe-(III)-(oxyhydr)oxides led to P release to the pore water and overlying water. The similarity in authigenic Ca-P concentrations in the sediment and suspended matter suggest that Ca-P is not formed in situ. The P burial efficiency was ≤ 32%. Hypoxia-driven sedimentary P recycling had a major impact on the water-column chemistry in the basin in 2012. Water-column monitoring data indicate up to ninefold higher surface water concentrations of phosphate in the basin in the late 1970s and a stronger hypoxia-driven seasonal P release from the sediment. The amplified release of P from the sediment in the past is attributed to the presence of a larger pool of Fe-bound P in the basin prior to the first onset of hypoxia. Given that P is not limiting, primary production in the basin has not been affected by the decadal changes in P availability and recycling over the past 40 years. The changes in P dynamics on decadal time scales were not recorded in sediment profiles of total P or organic C/total P.

Diffusive phosphorus fluxes in relation to the sediment phosphorus profile in Big Traverse Bay, Lake of the Woods

ABSTRACT James WF. 2017. Diffusive phosphorus fluxes in relation to the sediment phosphorus profile in Big Traverse Bay, Lake of the Woods. Lake Reserv Manage. 33: 360–368. The role of sediment diffusive phosphorus (P) flux in the P economy and cyanobacteria blooms in Lake of the Woods (LOW) is needed to establish total maximum daily load requirements. I quantified aerobic and anaerobic diffusive P fluxes as a function of temperature to estimate annual internal P loading in Big Traverse Bay of LOW. Replicate cores were collected seasonally and incubated at 5, 11, 18, and 25 C for rate determination. In addition, a sediment core collected in February 2015 was sectioned to analyze sediment P fractions and characterize P burial. Aerobic and anaerobic diffusive P fluxes varied nonlinearly with temperature. Rates were lowest under aerobic conditions, ranging between 0.05 and 0.36 mg/m2/d, and much higher under anaerobic conditions, ranging between 0.77 and 16.78 mg/m2/d, at 5 and 25 C, respectively. The annual diffusive P flux contribution to Big Traverse was 38 and 1172 mg/m2/yr under aerobic and anaerobic conditions, respectively, based on mean monthly bottom temperatures in 2015. The sediment vertical P profile exhibited a distinct surface maximum, suggesting an imbalance between gross deposition and burial. Assuming a constant sedimentation rate, potential annual internal P loading was higher at 246 mg/m2/yr compared to the annual aerobic diffusive P flux, suggesting anaerobic diffusive P flux and other unmeasured internal P loading processes contributed to the P budget. Low P burial efficiency and maintenance of a surface P bulge may be due to cyanobacteria-mediated biological uptake of sediment P, recycling, and redeposition to the sediment surface.

Sedimentary Phosphorus Speciation in the Coastal Hypoxic Area of Changjiang Estuary and Its Environmental Significance

Phosphorus (P) is a potential limiting nutrient in Changjiang Estuary. Sedimentary P preservation and regeneration play an important role in indicating regional environmental changes and buffering P limitation in the water column. A series of coring experiments was implemented in the hypoxic area of Changjiang Estuary to explore sedimentary P speciation and distribution and their environmental significance. The results showed that the contents and distributions of P in the cores were largely influenced by terrestrial loading, and Detr-P was the dominant P form in the sediments, followed by Org-P, Fe-P, and Auth-P, whereas Exch-P was the minor phase of Tot-P (<5%). Auth-P was predominantly yielded by Org-P and Fe-P transformations. P preservation in Changjiang Estuary was significantly related to terrestrial inputs and environmental changes in the water column. P speciation in cores tracked the regional environmental changes effectively. Distribution of reactive P in the hypoxic area was significantly different from that in the oxic area, with fairly high C/P ratios. The benthic diffusive flux of DRP in the study area ranged from 0.90 to 1.13 μmol·(cm2·a)-1. Tot-P burial efficiency (PBE) was higher than 70% and the PBE for Detr-P was nearly 100%, whereas the PBEs for Fe-P and Org-P were 38% and 26%, respectively. Auth-P was the dominant fraction of reactive P preserved in the sediments, and about 51% of Auth-P originated from Fe-P and Org-P transformations. The PBE in the hypoxia area of Changjiang Estuary was fairly lower than that in the continental shelf of the East China Sea. Hypoxia leads to a decrease in the PBE, which would have long-term influence on ecological environmental problems, especially eutrophification. Changes in terrestrial inputs played a key role in P composition in the sediments; the P loads of Changjiang River coupled with primary production and hypoxia greatly affected the P cycling in the Estuary.