scholarly journals Carbon sources supporting benthic mineralization in mangrove and adjacent seagrass sediments (Gazi Bay, Kenya)

2004 ◽  
Vol 1 (1) ◽  
pp. 311-333 ◽  
Author(s):  
S. Bouillon ◽  
T. Moens ◽  
F. Dehairs

Abstract. The origin of carbon substrates used by in situ sedimentary bacterial communities was investigated in an intertidal mangrove ecosystem and in adjacent seagrass beds in Gazi bay (Kenya) by δ13C analysis of bacteria-specific PLFA (phospholipid fatty acids) and bulk organic carbon. Export of mangrove-derived organic matter to the adjacent seagrass-covered bay was evident from sedimentary total organic carbon (TOC) and δ13CTOC data. PLFA δ13C data indicate that the substrate used by bacterial communities varied strongly and that exported mangrove carbon was a significant source for bacteria in the adjacent seagrass beds. Within the intertidal mangrove forest, bacterial PLFA at the surface layer (0-1 cm) typically showed more enriched δ13C values than deeper (up to 10 cm) sediment layers, suggesting a contribution from microphytobenthos and/or inwelled seagrass material. Under the assumption that seagrasses and mangroves are the dominant potential end-members, the estimated contribution of mangrove-derived carbon to benthic mineralization in the seagrass beds (16-74%) corresponds fairly well to the estimated contribution of mangrove C to the sedimentary organic matter pool (21-71%) across different seagrass sites. Based on these results and a compilation of literature data, we suggest that allochtonous carbon trapped in seagrass beds may often represent a significant fraction of the substrate for benthic mineralization - both in cases where seagrass C dominates the sediment TOC pool and in cases where external inputs are significant. Hence, it is likely that community respiration data systematically overestimate the role of mineralization in the overall seagrass C budget.

2004 ◽  
Vol 1 (1) ◽  
pp. 71-78 ◽  
Author(s):  
S. Bouillon ◽  
T. Moens ◽  
F. Dehairs

Abstract. The origin of carbon substrates used by in situ sedimentary bacterial communities was investigated in an intertidal mangrove ecosystem and in adjacent seagrass beds in Gazi bay (Kenya) by δ13C analysis of bacteria-specific PLFA (phospholipid fatty acids) and bulk organic carbon. Export of mangrove-derived organic matter to the adjacent seagrass-covered bay was evident from sedimentary total organic carbon (TOC) and δ13CTOC data. PLFA δ13C data indicate that the substrate used by bacterial communities varied strongly and that exported mangrove carbon was a significant source for bacteria in the adjacent seagrass beds. Within the intertidal mangrove forest, bacterial PLFA at the surface layer (0-1cm) typically showed more enriched δ13C values than deeper (up to 10cm) sediment layers, suggesting a contribution from microphytobenthos and/or inwelled seagrass material. Under the simplifying assumption that seagrasses and mangroves are the dominant potential end-members, the estimated contribution of mangrove-derived carbon to benthic mineralization in the seagrass beds (16-74%) corresponds fairly well to the estimated contribution of mangrove C to the sedimentary organic matter pool (21-71%) across different seagrass sites. Based on the results of this study and a compilation of literature data, we suggest that trapping of allochtonous C is a common feature in seagrass beds and often represents a significant source of C for sediment bacteria - both in cases where seagrass C dominates the sediment TOC pool and in cases where external inputs are significant. Hence, it is likely that data on community respiration rates systematically overestimate the role of in situ mineralization as a fate of seagrass production.


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.


2019 ◽  
Vol 37 (3) ◽  
pp. 263-273
Author(s):  
Efraín Francisco Visconti-Moreno ◽  
Ibonne Geaneth Valenzuela-Balcázar

The stability of soil aggregates depends on the organic matter, and the soil use and management can affect the soil organicmatter (SOM) content. Therefore, it is necessary to know therelationship between aggregate stability and the content of SOMin different types of soil use at two different altitudes of theColombian Andes. This study examined the conditions of soilaggregate stability expressed as a distribution of the size classes of stable aggregates (SA) and of the mean weighted diameter of the stable aggregates (MWD). To correlate these characteristics with the soil organic carbon (OC), we measured the particulate organic matter pool (POC), the OC associated with the mineral organic matter pool (HOC), the total organic carbon content (TOC), and the humification rate (HR). Soils were sampled at two altitudes: 1) Humic Dystrudepts in a cold tropical climate (CC) with three plots: tropical mountain rainforest, pastures, and crops; 2) Fluvaquentic Dystrudepts in a warm tropical climate (WC) with three plots: tropical rainforest, an association of oil palm and pastures, and irrigated rice. Soils were sampled at three depths: 0-5, 5-10 and 10-20 cm. The physical properties, mineral particle size distribution, and bulk density were measured. The content of SA with size>2.36 mm was higher in the CC soil (51.48%) than in the WC soil (9.23%). The SA with size 1.18-2.36 mm was also higher in the CC soil (7.78%) than in the WC soil (0.62%). The SA with size 0.60-1.18 mm resulted indifferent. The SA with size between 0.30 and 0.60 mm were higher in the WC soil (13.95%) than in the CC soil (4.67%). The SA<0.30 mm was higher in the WC soil (72.56%) than in the CC soil (32.15%). It was observed that MWD and the SA>2.36 mm increased linearly with a higher POC, but decreased linearly with a higher HR. For the SA<0.30 mm, a linear decrease was observed at a higher POC, while it increased at a higher HR.


Radiocarbon ◽  
2007 ◽  
Vol 49 (2) ◽  
pp. 1079-1091 ◽  
Author(s):  
Janet Rethemeyer ◽  
Pieter M Grootes ◽  
Sonja Brodowski ◽  
Bernard Ludwig

Changes in soil organic carbon stocks were simulated with the Rothamsted carbon (RothC) model. We evaluated the calculation of a major input variable, the amount of inert organic matter (IOM), using measurable data. Three different approaches for quantifying IOM were applied to soils with mainly recent organic matter and with carbon contribution from fossil fuels: 1) IOM estimation via total soil organic carbon (SOC); 2) through bulk soil radiocarbon and a mass balance; and 3) by quantifying the portion of black carbon via a specific marker. The results were highly variable in the soil containing lignite-derived carbon and ranged from 8% to 52% inert carbon of total SOC, while nearly similar amounts of 5% to 8% were determined in the soil with mainly recent organic matter. We simulated carbon dynamics in both soils using the 3 approaches for quantifying IOM in combination with carbon inputs derived from measured crop yields. In the soil with recent organic matter, all approaches gave a nearly similar good agreement between measured and modeled data, while in the soil with a fossil carbon admixture, only the 14C approach was successful in matching the measured data. Although 14C was useful for initializing RothC, care should be taken when interpreting SOC dynamics in soils containing carbon from fossil fuels, since these reflect the contribution from both natural and anthropogenic carbon sources.


2021 ◽  
Vol 9 (4) ◽  
pp. 823-844
Author(s):  
Thomas Croissant ◽  
Robert G. Hilton ◽  
Gen K. Li ◽  
Jamie Howarth ◽  
Jin Wang ◽  
...  

Abstract. In mountain ranges, earthquakes can trigger widespread landsliding and mobilize large amounts of organic carbon by eroding soil and vegetation from hillslopes. Following a major earthquake, the landslide-mobilized organic carbon can be exported from river catchments by physical sediment transport processes or stored within the landscape where it may be degraded by heterotrophic respiration. The competition between these physical and biogeochemical processes governs a net transfer of carbon between the atmosphere and sedimentary organic matter, yet their relative importance following a large landslide-triggering earthquake remains poorly constrained. Here, we propose a model framework to quantify the post-seismic redistribution of soil-derived organic carbon. The approach combines predictions based on empirical observations of co-seismic sediment mobilization with a description of the physical and biogeochemical processes involved after an earthquake. Earthquake-triggered landslide populations are generated by randomly sampling a landslide area distribution, a proportion of which is initially connected to the fluvial network. Initially disconnected landslide deposits are transported downslope and connected to rivers at a constant velocity in the post-seismic period. Disconnected landslide deposits lose organic carbon by heterotrophic oxidation, while connected deposits lose organic carbon synchronously by both oxidation and river export. The modeling approach is numerically efficient and allows us to explore a large range of parameter values that exert a control on the fate of organic carbon in the upland erosional system. We explore the role of the climatic context (in terms of mean annual runoff and runoff variability) and rates of organic matter degradation using single pool and multi-pool models. Our results highlight the fact that the redistribution of organic carbon is strongly controlled by the annual runoff and the extent of landslide connection, but less so by the choice of organic matter degradation model. In the context of mountain ranges typical of the southwestern Pacific region, we find that model configurations allow more than 90 % of the landslide-mobilized carbon to be exported from mountain catchments. A simulation of earthquake cycles suggests efficient transfer of organic carbon out of a mountain range during the first decade of the post-seismic period. Pulsed erosion of organic matter by earthquake-triggered landslides is therefore an effective process to promote carbon sequestration in sedimentary deposits over thousands of years.


2015 ◽  
Vol 112 (19) ◽  
pp. 5909-5914 ◽  
Author(s):  
Bethanie R. Edwards ◽  
Kay D. Bidle ◽  
Benjamin A. S. Van Mooy

Diatoms and other phytoplankton play a crucial role in the global carbon cycle, fixing CO2into organic carbon, which may then be exported to depth via sinking particles. The molecular diversity of this organic carbon is vast and many highly bioactive molecules have been identified. Polyunsaturated aldehydes (PUAs) are bioactive on various levels of the marine food web, and yet the potential for these molecules to affect the fate of organic carbon produced by diatoms remains an open question. In this study, the effects of PUAs on the natural microbial assemblages associated with sinking particles were investigated. Sinking particles were collected from 150 m in the water column and exposed to varying concentrations of PUAs in dark incubations over 24 h. PUA doses ranging from 1 to 10 µM stimulated respiration, organic matter hydrolysis, and cell growth by bacteria associated with sinking particles. PUA dosages near 100 µM appeared to be toxic, resulting in decreased bacterial cell abundance and metabolism, as well as pronounced shifts in bacterial community composition. Sinking particles were hot spots for PUA production that contained concentrations within the stimulatory micromolar range in contrast to previously reported picomolar concentrations of these compounds in bulk seawater. This suggests PUAs produced in situ stimulate the remineralization of phytoplankton-derived sinking organic matter, decreasing carbon export efficiency, and shoaling the average depths of nutrient regeneration. Our results are consistent with a “bioactivity hypothesis” for explaining variations in carbon export efficiency in the oceans.


Ecosystems ◽  
2021 ◽  
Author(s):  
Benoît O. L. Demars ◽  
Joanna L. Kemp ◽  
Baptiste Marteau ◽  
Nikolai Friberg ◽  
Barry Thornton

AbstractThe annual global loss of organic carbon from terrestrial ecosystems into rivers is similar to the organic carbon stored in soils each year. Dissolved organic matter (DOM) flows through the food web to macroinvertebrates, but little is known about the effect of DOM increase on stream food webs and how much macroinvertebrates may contribute to the regulation of carbon fluxes in rivers. Using a before and after control impact (BACI) experimental design, we increased by 12% (+ 0.52 mg C L−1) the concentration of DOM in a stream for three weeks by adding sucrose, with a distinctive δ13C signature, to simulate a pulse of natural DOM supply from soils. We partitioned the diet of macroinvertebrates from carbon sources according to the green pathway (autotrophs) and detrital pathways (bacteria and terrestrial organic matter). Our flow food web approach based on C fluxes, with bacteria as a key node, showed the dominant contribution of the detrital pathways for macroinvertebrates in the reference stream. DOM addition induced changes in the diets of individual taxa, but did not have any strong effects on the relative overall contribution of the detrital pathways versus the green pathway. Autotrophic uptake of CO2 respired by bacteria was much larger than bacterial C flux to invertebrates (that is, the classic microbial loop) and allowed a significant fraction of natural allochthonous organic carbon to make its way to macroinvertebrates via autotrophs fixing CO2 respired by bacteria. Overall macroinvertebrates did not regulate directly to any great extent the flux of stream DOM towards downstream ecosystems.


1982 ◽  
Vol 39 (12) ◽  
pp. 1699-1718 ◽  
Author(s):  
Robert J. Naiman

Estimates of the amount of material moving annually from terrestrial ecosystems to the ocean are largely based on an incomplete understanding of events occurring throughout the hydrologic year, and only a vague comprehension of in-stream processes controlling that export. Discharge, suspended sediment, particulate organic matter (POM; > 0.5 μm), dissolved organic carbon (DOC; <0.5 μm diameter), and the percentage of organic matter were measured from 1979 to 1981 in five pristine Quebec streams: First Choice Creek (1st order; watershed area: 0.25 km2), Beaver Creek (2nd order; 1.83 km2), Muskrat River (5th order; 204 km2), Matamek River (6th order; 673 km2), and the Moisie River (9th order; 19 871 km2). All streams, with the exception of First Choice Creek, have a strong spring freshet when 43–55% of the annual discharge occurs. By describing sediment and organic carbon export throughout the annual hydrologic cycle, 1 showed that during the 2-mo spring freshet 71–92% of the annual sediment load is exported but only 59–65% of the annual POM load, and only 47–51% of the annual DOC load. Sediment yield is relatively constant between watersheds (1.5–7.6 g∙m−2∙yr−1), as is POM export (1.0–6.7 g ash-free dry-weight [AFDW]∙m−2∙yr−1); however, export DOC varies from 3.1 g C∙m−2∙yr−1 in First Choice Creek to 48.4 g C∙m−2∙yr−1 in Beaver Creek. There appears to be rapid loading of carbon between 1st- and 2nd-order streams in boreal forests, followed by biological and physical processing as watershed area increases. Thus, for the Moisie River watershed, export of total organic carbon (TOC) is reduced to only 4.7 g C∙m−2∙yr−1. Export of coarse particulate organic matter (> 1 mm) is negligible (normally < 0.1 mg∙L−1), as is oxidation of the suspended load (< 0.5%∙d−1). Effects of summer storms, natural diel variations, and depth of sample from the water column are shown to have a minimal influence on concentrations. Rating curves (kg∙d−1 vs. discharge) are developed to estimate the annual yield of sediment, POM, and DOC, and to evaluate long-term variations. From the results I suggest that in-stream processing and retention devices exert considerable control over the quantity and nature of suspended organic material. Physical processes such as the discharge regime and stream power are relatively less important in determining organic concentrations, but more important in determining sediment concentrations.Key words: seston, carbon, sediment, boreal forest, watershed, river, stream, export


2020 ◽  
Vol 17 (12) ◽  
pp. 3277-3298
Author(s):  
Sarah Z. Rosengard ◽  
Robert W. Izett ◽  
William J. Burt ◽  
Nina Schuback ◽  
Philippe D. Tortell

Abstract. We report results from two Lagrangian drifter surveys off the Oregon coast, using continuous shipboard sensors to estimate mixed-layer gross primary productivity (GPP), community respiration (CR), and net community production (NCP) from variations in biological oxygen saturation (ΔO2∕Ar) and optically derived particulate organic carbon (POC). At the first drifter survey, conducted in a nearshore upwelling zone during the development of a microplankton bloom, net changes in ΔO2∕Ar and [POC] were significantly decoupled. Differences in GPP and NCP derived from ΔO2∕Ar (NCPO2/Ar) and POC (NCPPOC) time series suggest the presence of large POC losses from the mixed layer. At this site, we utilized the discrepancy between NCPO2/Ar and NCPPOC, and additional constraints derived from surface water excess nitrous oxide (N2O), to evaluate POC loss through particle export, DOC production, and vertical mixing fluxes. At the second drifter survey, conducted in lower-productivity, density-stratified offshore waters, we also observed offsets between ΔO2∕Ar and POC-derived GPP and CR rates. At this site, however, net [POC] and ΔO2∕Ar changes yielded closer agreement in NCP estimates, suggesting a tighter relationship between production and community respiration, as well as lower POC loss rates. These results provide insight into the possibilities and limitations of estimating productivity from continuous underway POC and ΔO2∕Ar data in contrasting oceanic waters. Our observations support the use of diel POC measurements to estimate NCP in lower-productivity waters with limited vertical carbon export and the potential utility of coupled O2 and optical measurements to estimate the fate of POC in high-productivity regions with significant POC export.


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