Biological mineralization of organic matter in the modern virgin and plowed chernozems, buried chernozems, and fossil chernozems

2009 ◽  
Vol 42 (10) ◽  
pp. 1109-1119 ◽  
Author(s):  
I. V. Ivanov ◽  
L. S. Pesochina ◽  
V. M. Semenov
2008 ◽  
Vol 41 (7) ◽  
pp. 717-730 ◽  
Author(s):  
V. M. Semenov ◽  
L. A. Ivannikova ◽  
T. V. Kuznetsova ◽  
N. A. Semenova ◽  
A. S. Tulina

Carbonate concretions attract study because, unlike intergranular cements, they form conspicuous spheroidal or laterally extensive bodies. However, they pose a fundamental challenge to uniformitarianism because no concretions identical to geologically preserved ones are forming today. Nevertheless, understanding their origin can be accomplished by simulation of geological processes, using present-day processes and pore-water compositions. The successive reactions (mainly microbial) degrading organic-matter during sediment burial produce inorganic species which may form carbonate and sulphide minerals and can be characterized by stable isotope and chemical compositions. Pyrite-rimmed, spheroidal carbonate carbonate concretions (Jurassic) resulted from outward diffusion of microbially produced sulphide which reacted with inwardly diffusing iron. Extensive, bedded siderite concretions (Coal Measures) were formed by microbial reduction of Fe(III) which could only proceed because the reaction was buffered by precipitation of carbonate produced by methanogens degrading more deeply buried organic matter. Byproducts of the reactions may either inhibit or promote initiation of similar precipitation reactions locally. The former case leads to situations where initial random localization of reaction sites causes self-organized reaction within the sediment (applicable to the Jurassic example). Simulations of the Jurassic concretions’ growth process, using present day pore-water solute concentrations of calcium, sulphide and iron, give results which correspond with the spatial distribution of mineral precipitates observed in geological samples. Calculated rates of mineral precipitation give minimum durations 7400 to 52000 years, much shorter than previous estimates. These results suggest that low rates of microbial sulphate reduction, relative to present day measured values, were needed and accord with the inferred depth of formation and pore-water sulphate concentrations.


2020 ◽  
Vol 17 (18) ◽  
pp. 4571-4589
Author(s):  
François Clayer ◽  
Yves Gélinas ◽  
André Tessier ◽  
Charles Gobeil

Abstract. The complexity of organic matter (OM) degradation mechanisms represents a significant challenge for developing biogeochemical models to quantify the role of aquatic sediments in the climate system. The common representation of OM by carbohydrates formulated as CH2O in models comes with the assumption that its degradation by fermentation produces equimolar amounts of methane (CH4) and dissolved inorganic carbon (DIC). To test the validity of this assumption, we modelled using reaction-transport equation vertical profiles of the concentration and isotopic composition (δ13C) of CH4 and DIC in the top 25 cm of the sediment column from two lake basins, one whose hypolimnion is perennially oxygenated and one with seasonal anoxia. Furthermore, we modelled solute porewater profiles reported in the literature for four other seasonally anoxic lake basins. A total of 17 independent porewater datasets are analyzed. CH4 and DIC production rates associated with methanogenesis at the five seasonally anoxic sites collectively show that the fermenting OM has a mean (± SD) carbon oxidation state (COS) value of -1.4±0.3. This value is much lower than the value of zero expected from carbohydrate fermentation. We conclude that carbohydrates do not adequately represent the fermenting OM in hypolimnetic sediments and propose to include the COS in the formulation of OM fermentation in models applied to lake sediments to better quantify sediment CH4 outflux. This study highlights the potential of mass balancing the products of OM mineralization to characterize labile substrates undergoing fermentation in sediments.


EDIS ◽  
2019 ◽  
Vol 2019 (1) ◽  
Author(s):  
James Mabry McCray

Potassium is a primary plant nutrient that is required in large amounts by sugarcane. About 74% of the 400,000 acres of Florida sugarcane is grown on organic soils in the Everglades Agricultural Area. Potassium is not a component of organic matter and virgin Histosols contain very low concentrations of K, so release of K through mineralization of organic matter in these soils is not an adequate K source for plant growth. This 7-page document presents revised potassium fertilizer recommendations for sugarcane grown on Florida organic soils along with supporting information. Written by J. Mabry McCray, and published by the UF/IFAS Agronomy Department, February 2019.  http://edis.ifas.ufl.edu/ag428


2017 ◽  
Vol 10 (1) ◽  
pp. 453-482 ◽  
Author(s):  
Evgeniy V. Yakushev ◽  
Elizaveta A. Protsenko ◽  
Jorn Bruggeman ◽  
Philip Wallhead ◽  
Svetlana V. Pakhomova ◽  
...  

Abstract. Interactions between seawater and benthic systems play an important role in global biogeochemical cycling. Benthic fluxes of some chemical elements (e.g., C, N, P, O, Si, Fe, Mn, S) alter the redox state and marine carbonate system (i.e., pH and carbonate saturation state), which in turn modulate the functioning of benthic and pelagic ecosystems. The redox state of the near-bottom layer in many regions can change with time, responding to the supply of organic matter, physical regime, and coastal discharge. We developed a model (BROM) to represent key biogeochemical processes in the water and sediments and to simulate changes occurring in the bottom boundary layer. BROM consists of a transport module (BROM-transport) and several biogeochemical modules that are fully compatible with the Framework for the Aquatic Biogeochemical Models, allowing independent coupling to hydrophysical models in 1-D, 2-D, or 3-D. We demonstrate that BROM is capable of simulating the seasonality in production and mineralization of organic matter as well as the mixing that leads to variations in redox conditions. BROM can be used for analyzing and interpreting data on sediment–water exchange, and for simulating the consequences of forcings such as climate change, external nutrient loading, ocean acidification, carbon storage leakage, and point-source metal pollution.


2019 ◽  
Vol 37 ◽  
Author(s):  
C.C. MATOS ◽  
M.D. COSTA ◽  
I.R. SILVA ◽  
A.A. SILVA

ABSTRACT: The competition between weeds and crops is one of the main factors responsible for productivity losses in agricultural fields. This review aimed at presenting and discussing how the interactions between weeds and microorganisms can affect the competitive capacity of weeds and soil physicochemical properties. We also discuss how changes in the elemental stoichiometry of weeds can reflect their competitive and adaptative capacity. Although weeds are more dependent on associations with soil microorganisms than crops for growth, few studies have assessed the contribution of the soil microbiota to their competitive success in agroecosystems. When in competition, plants can change the elemental stoichiometry of their tissues in environments with varied nutrient availability. Elemental stoichiometry of plants has been particularly well studied using ecological approaches on the dynamics of weed populations in natural ecosystems, being a promising tool for understanding weed capacity to adapt to different agricultural managements. Plants control the biogeochemical cycles of carbon (C) and nitrogen (N) in the rhizosphere through a phenomenon known as the rhizosphere priming effect (RPE). Although this review has found some information in the literature that provides strong indications that the coexistence of weeds and crops may increase soil organic matter mineralization, we are not aware of studies investigating the effects of competition among these plants on RPE.


1984 ◽  
Vol 50 (1) ◽  
pp. 96-97
Author(s):  
J. J. Olie ◽  
C. L. M. Steenbergen ◽  
H. Verdouw ◽  
Th. E. Cappenberg

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