Carboxyl-richness controls organic carbon preservation during coprecipitation with iron (oxyhydr)oxides in the natural environment

The coprecipitation of organic carbon with iron minerals is important for its preservation in soils and sediments, but the mechanisms for carbon-iron interactions and thus the controls on organic carbon cycling are far from understood. Here we coprecipitate carboxylic acids with iron (oxyhydr)oxide ferrihydrite and use near-edge X-ray absorption fine structure spectroscopy and wet chemical treatments to determine the relationship between sequestration mechanism and organic carbon stability against its release and chemical oxidative remineralisation. We show that organic carbon sequestration, stabilisation and persistence increase with an increasing number of carboxyl functional groups. We suggest that carboxyl-richness provides an important control on organic carbon preservation in the natural environment. Our work offers a mechanistic basis for understanding the stability and persistence of organic carbon in soils and sediments, which might be used to develop an overarching relationship between organic functional group-richness, mineral interactions and organic carbon preservation in the Earth system.

Fluvial organic carbon cycling regulated by sediment transit time and mineral protection

Rivers transfer terrestrial organic carbon (OC) from mountains to ocean basins, playing a key role in the global carbon cycle. During fluvial transit, OC may be oxidized and emitted to the atmosphere as CO2 or preserved and transported to downstream depositional sinks. The balance between oxidation and preservation determines the amount of particulate OC (POC) that can be buried long term, but the factors regulating this balance are poorly constrained. Here, we quantify the effects of fluvial transit on POC fluxes along an ~1,300 km lowland channel with no tributaries. We show that sediment transit time and mineral protection regulate the magnitude and rate of POC oxidation, respectively. Using a simple turnover model, we estimate that annual POC oxidation is a small percentage of the POC delivered to the river. Modelling shows that lateral erosion into POC-rich floodplains can increase POC fluxes to downstream basins, thereby offsetting POC oxidation. Consequently, rivers with high channel mobility can enhance CO2 drawdown while management practices that stabilize river channels may reduce the potential for CO2 drawdown.

Aquatic Eddy Covariance: The Method and Its Contributions to Defining Oxygen and Carbon Fluxes in Marine Environments

Aquatic eddy covariance (AEC) is increasingly being used to study benthic oxygen (O2) flux dynamics, organic carbon cycling, and ecosystem health in marine and freshwater environments. Because it is a noninvasive technique, has a high temporal resolution (∼15 min), and integrates over a large area of the seafloor (typically 10–100 m2), it has provided new insights on the functioning of aquatic ecosystems under naturally varying in situ conditions and has given us more accurate assessments of their metabolism. In this review, we summarize biogeochemical, ecological, and biological insights gained from AEC studies of marine ecosystems. A general finding for all substrates is that benthic O2 exchange is far more dynamic than earlier recognized, and thus accurate mean values can only be obtained from measurements that integrate over all timescales that affect the local O2 exchange. Finally, we highlight new developments of the technique, including measurements of air–water gas exchange and long-term deployments. Expected final online publication date for the Annual Review of Marine Science, Volume 14 is January 2022. Please see http://www.annualreviews.org/page/journal/pubdates for revised estimates.

DIVERSITY AND DISTRIBUTION OF SOIL FUNGI ISOLATED FROM THE CABBAGE (BRASSICA OLERACEA VAR. CAPITATA) RHIZOSPHERE

We have been working on the traditional way to discourse microscopic fungal population present in the rhizospheric soil of Cabbage (Brassica oleracea var. capitata). These fungi are crucial for the decomposition of organic carbon, cycling of nitrogen and phosphorus, and belowground carbon sequestration. Their role as parasite, saprophyte, mutualism and commensalism is also well established. The objective of this study was to analyze soil and determine the fungus genera from the rhizospheric soil of Cabbage from the area of Armpora, Binner, Chakloo, Janbazpora, Ladoora, Muslimabad, Nadihal and Punchatra villages which come under, Dist. Baramulla, Jammu and Kashmir. The Cabbage plant rhizospheric soil was obtained from various research locations marked from the said villages. Research method applied was a survey with the intent of soil sampling. The soil samples were taken from 1-10 cm deep soil for sampling purpose. The result recorded from soil samples were then analyzed descriptively and described based on their macro and micro morphology. Then, the collected fungus was identified by using identification manual for fungus. Fungi such as Aspergillus, Alternaria, Chaetomium, Cladosporium, Curvularia, Fusarium, Mortirella, Mucor, Nigrospora, Penicillium, Rhizoctonia, Phoma, Trichoderma, Verticillium and Sterilia mycelia were most frequently recorded.

Uncoupled seasonal variability of transparent exopolymer and Coomassie stainable particles in coastal Mediterranean waters

Transparent exopolymer particles (TEP) and Coomassie stainable particles (CSP) are gel-like particles, ubiquitous in the ocean, that affect important biogeochemical processes including organic carbon cycling by planktonic food webs. Despite much research on both groups of particles (especially TEP) over many years, whether they exist as distinctly stainable fractions of the same particles or as independent particles, each with different driving factors, remains unclear. To address this question, we examined the temporal dynamics of TEP and CSP over 2 complete seasonal cycles at 2 coastal sites in the Northwestern Mediterranean Sea, the Blanes Bay Microbial Observatory (BBMO) and the L’Estartit Oceanographic Station (EOS), as well as their spatial distribution along a coast-to-offshore transect. Biological, chemical, and physical variables were measured in parallel. Surface concentrations (mean ± standard deviation [SD]) of TEP were 36.7 ± 21.5 µg Xanthan Gum (XG) eq L–1 at BBMO and 36.6 ± 28.3 µg XG eq L–1 at EOS; for CSP, they were 11.9 ± 6.1 µg BSA eq L–1 at BBMO and 13.0 ± 5.9 µg BSA eq L–1 at EOS. Seasonal variability was more evident at EOS, where surface TEP and CSP concentrations peaked in summer and spring, respectively, and less predictable at the shore-most station, BBMO. Vertical distributions between surface and 80 m, monitored at EOS, showed highest TEP concentrations within the surface mixed layer during the stratification period, whereas CSP concentrations were highest before the onset of summer stratification. Phytoplankton were the main drivers of TEP and CSP distributions, although nutrient limitation and saturating irradiance also appeared to play important roles. The dynamics and distribution of TEP and CSP were uncoupled both in the coastal sites and along the transect, suggesting that they are different types of particles produced and consumed differently in response to environmental variability.

Microbial sulfate reduction and organic sulfur formation in sinking marine particles

Climate change is driving an expansion of marine oxygen-deficient zones, which may alter the global cycles of carbon, sulfur, nitrogen, and trace metals. Currently, however, we lack a full mechanistic understanding of how oxygen deficiency affects organic carbon cycling and burial. Here, we show that cryptic microbial sulfate reduction occurs in sinking particles from the eastern tropical North Pacific oxygen-deficient zone and that some microbially produced sulfide reacts rapidly to form organic sulfur that is resistant to acid hydrolysis. Particle-hosted sulfurization could enhance carbon preservation in sediments underlying oxygen-deficient water columns and serve as a stabilizing feedback between expanding anoxic zones and atmospheric carbon dioxide. A similar mechanism may help explain more-extreme instances of organic carbon preservation associated with marine anoxia in Earth history.

A multi-isotope model for simulating soil organic carbon cycling in eroding landscapes (WATEM_C v1.0)

There is increasing recognition that lateral soil organic carbon (SOC) fluxes due to erosion have imposed an important impact on the global C cycling. Field and experimental studies have been conducted to investigate this topic. It is useful to have a modeling tool that takes into account various soil properties and has flexible resolution and scale options so that it can be widely used to study relevant processes and evaluate the effect of soil erosion on SOC cycling. This study presents a model that is capable of simulating SOC cycling in landscapes that are subjected to erosion. It considers all three C isotopes (12C, 13C and 14C) with flexible time steps and a detailed vertical solution of the soil profile. The model also represents radionuclide cycling in soils that can assist in constraining the lateral and vertical redistribution of soil particles within landscapes. The model gives a three-dimensional representation of soil properties including 137Cs activity, SOC stock, and δ13C and Δ14C values. Using the same C cycling processes in stable, eroding and depositional areas, our model is able to reproduce the observed spatial and vertical patterns of C contents, δ13C values, and Δ14C values. This indicates that at the field scale with a similar C decomposition rate, physical soil redistribution is the main cause of the spatial variability of these C metrics.