Studies on the Sediment of St. Margaret's Bay, Nova Scotia

1979 ◽  
Vol 36 (5) ◽  
pp. 529-536 ◽  
Author(s):  
T. G. Hughes

A detailed examination of the sediment in a small area of St. Margaret's Bay revealed it to be composed of two main types of particles, mineral particles and particles of organic debris. Debris was also adsorbed onto the mineral particles. Particles generally had relatively low numbers of bacteria associated with them indicating that most of the organic carbon in the sediment is refractory. Variation in size distribution of the component particles with depth in the sediment was found to be minimal, but a slight decrease in the proportion of debris particles was seen. Variation in size distribution along a transect was also limited, but where the mineral particles became coarser the size range of the debris particles remained constant. The relative amount of debris particles along the transect varied little but values for total organic carbon (by weight) changed dramatically. Key words: sediment, particle composition, size distribution, organic carbon

Author(s):  
Magdalena Banach-Szott ◽  
Bozena Debska ◽  
Erika Tobiasova

AbstractMany studies report organic carbon stabilization by clay minerals, but the effects of land use and soil type on the properties of humic acids (HAs) are missing. The aim of the paper is to determine the effects of land use and soil types on the characteristics of HAs, which have a considerable influence on organic matter quality. It was hypothesised that the effect of the land use on HAs properties depends on the particular size distribution. The research was performed in three ecosystems: agricultural, forest, and meadow, located in Slovakia. From each of them, the samples of 4 soil types were taken: Chernozem, Luvisol, Planosol, and Cambisol. The soil samples were assayed for the content of total organic carbon (TOC) and the particle size distribution. HAs were extracted with the Schnitzer method and analysed for the elemental composition, spectrometric parameters in the UV-VIS range, and hydrophilic and hydrophobic properties, and the infrared spectra were produced. The research results have shown that the properties of HAs can be modified by the land use and the scope and that the direction of changes depends on the soil type. The HAs of Chernozem and Luvisol in the agri-ecosystem were identified with a higher “degree of maturity”, as reflected by atomic ratios (H/C, O/C, O/H), absorbance coefficients, and the FT-IR spectra, as compared with the HAs of the meadow and forest ecosystem. However, as for the HAs of Cambisol, a higher “degree of maturity” was demonstrated for the meadow ecosystem, as compared with the HAs of the agri- and forest ecosystem. The present research has clearly identified that the content of clay is the factor determining the HAs properties. Soils with a higher content of the clay fraction contain HAs with a higher “degree of maturity”.


2003 ◽  
Vol 3 (6) ◽  
pp. 5513-5546 ◽  
Author(s):  
M. Ketzel ◽  
P. Wåhlin ◽  
A. Kristensson ◽  
E. Swietlicki ◽  
R. Berkowicz ◽  
...  

Abstract. Particle size distribution (size-range 3–900 nm) and PM10 was measured simultaneously at an urban background station in Copenhagen, a near-city background and a rural location during a period in September-November 2002. The study investigates the contribution from urban versus regional sources of particle number and mass concentration. The total particle number (ToN) and NOx are well correlated at the urban and near-city level and show a distinct diurnal variation, indicating the common traffic source. The average ToN at the three stations differs by a factor of 3. The observed concentrations are 2500 # cm−3, 4500 # cm−3 and 7700 # cm−3 at rural, near-city and urban level, respectively. PM10 and total particle volume (ToV) are well correlated between the three different stations and show similar concentration levels, in average within 30% relative difference, indicating a common source from long-range transport that dominates the concentrations at all locations. Measures to reduce the local urban emissions of NOx and ToN are likely to affect both the street level and urban background concentrations, while for PM10 and ToV only measurable effects at the street level are probable. Taking into account the supposed stronger health effects of ultrafine particles reduction measures should address particle number emissions. The traffic source contributes strongest in the 10–200 nm particle size range. The maximum of the size distribution shifts from about 20–30 nm at kerbside to 50–60 nm at rural level. We also observe particle formation events in the 3–20 nm size range at rural location in the afternoon hours, mainly under conditions with low concentrations of pre-existing aerosol particles. The maximum in the size distribution of the "traffic contribution" seems to be shifted to about 28 nm in the urban location compared to 22 nm at kerbside. Assuming NOx as an inert tracer on urban scale let us estimate that ToN at urban level is reduced by 15–30% compared to kerbside. Particle removal processes, e.g. deposition and coagulation, which are most efficient for smallest particle sizes (<20 nm) and condensational growth are likely mechanisms for the loss of particle number and the shift in particle size.


2019 ◽  
Vol 85 (10) ◽  
Author(s):  
Tao Wang ◽  
Zhaomo Tian ◽  
Anders Tunlid ◽  
Per Persson

ABSTRACT The interactions between dissolved organic matter (DOM) and mineral particles are critical for the stabilization of soil organic matter (SOM) in terrestrial ecosystems. The processing of DOM by ectomycorrhizal fungi contributes to the formation of mineral-stabilized SOM by two contrasting pathways: the extracellular transformation of DOM (ex vivo pathway) and the secretion of mineral-surface-reactive metabolites (in vivo pathway). In this study, we examined how changes in nitrogen (N) availability affected the formation of mineral-associated carbon (C) from these two pathways. DOM was extracted from forest soils. The processing of this DOM by the ectomycorrhizal fungus Paxillus involutus was examined in laboratory-scale studies with different levels of ammonium. At low levels of ammonium (i.e., under N-limited conditions), the DOM components were slightly oxidized, and fungal C metabolites with iron-reducing activity were secreted. Ammonium amendments decreased the amount of C metabolites, and no additional oxidation of the organic matter was detected. In contrast, the hydrolytic activity and the secretion of N-containing compounds increased, particularly when high levels of ammonium were added. Under these conditions, C, but not N, limited fungal growth. Although the overall production of mineral-associated organic C was not affected by ammonium concentrations, the observed shifts in the activities of the ex vivo and in vivo pathways affected the composition of organic matter adsorbed onto the mineral particles. Such changes will affect the properties of organic matter-mineral associations and, thus, ultimately, the stabilization of SOM. IMPORTANCE Nitrogen (N) availability plays a critical role in the cycling and storage of soil organic matter (SOM). However, large uncertainties remain in predicting the net effect of N addition on soil organic carbon (C) storage due to the complex interactions between organic matter, microbial activity, and mineral particles that determine the formation of stable SOM. Here, we attempted to disentangle the effects of ammonium on these interactions in controlled microcosm experiments including the ectomycorrhizal fungus P.involutus and dissolved organic matter extracted from forest soils. Increased ammonium levels affected the fungal processing of the organic material as well as the secretion of extracellular metabolites. Although ammonium additions did not increase the net production of mineral-adsorbed C, changes in the decomposition and secretion pathways altered the composition of the adsorbed organic matter. These changes may influence the properties of the organic matter-mineral associations and, thus, the stabilization of SOM.


1997 ◽  
Vol 1 (3) ◽  
pp. 661-669 ◽  
Author(s):  
S. Hughes ◽  
B. Reynolds ◽  
J. A. Hudson ◽  
C. Freeman

Abstract. In a field experiment to investigate potential impacts of climatic change, a small area of flush wetland in Wales was subjected to three successive years of simulated summer drought/rewetting (autumn-spring) cycles (1992–94). Drought was simulated achieved by diverting stream water around the experimental wetland during the summer, so that the wetland received only precipitation inputs during that time. The effects on peat-water chemistry in the rhizosphere were monitored at regular intervals until spring 1996, and comparisons made with a control. Simulated summer drought decreased, significantly, the natural summer peaks in dissolved organic carbon (DOC) and iron, whilst subsequently increasing the natural autumn-winter peaks in sulphate concentrations and acidity in the peat water. The effects of simulated drought on SO4 concentrations in the peat water compared favourably with subsequent events monitored following a natural summer drought in 1995. Autumn-winter peaks in SO4 concentrations in the control wetland following the natural drought were of similar magnitude to those induced by the drought simulated in the experimental wetland in the previous three years.


Minerals ◽  
2020 ◽  
Vol 10 (11) ◽  
pp. 1040
Author(s):  
Martin Couillard ◽  
Daniel D. Tyo ◽  
David M. Kingston ◽  
Bussaraporn Patarachao ◽  
Andre Zborowski ◽  
...  

A primary concern of commercial mined oil sands operations is the extent to which one can minimize the content of water and solids contaminants in the solvent-diluted bitumen products resulting from the bitumen production processes. During bitumen production, particles of about 2 µm or less may be responsible for the stabilization of water-in-bitumen emulsions that form during aqueous extraction of bitumen and purification of bitumen froth subsequently during the froth treatment processes, thus leading to the presence of those contaminants in solvent-diluted bitumen products. In this study, we separate and analyze sub-2 µm clay solids isolated from typical bitumen froth fed to a froth treatment plant at a commercial mined oil sands operation. Analytical transmission electron microscopy (TEM) with spatially-resolved energy-dispersive X-ray spectroscopy (EDX) and electron energy-loss spectroscopy (EELS) demonstrate key differences in morphology and composition between sub-2 µm clay aggregates with two distinct wettability characteristics: hydrophilic vs. biwettable particle surfaces. In particular, clay platelets with <200 nm lateral dimensions and thicknesses of a few atomic layers, which are intermixed within coarser sub-2 µm clay aggregates, are found to confer clear differences in morphological characteristics and wettability behaviors to the sub-2 µm clay aggregates. The <200 nm clay platelets found within sub-2 µm biwettable clays tend to arrange themselves with random orientations, whereas <200 nm clay platelets within sub-2 µm hydrophilic clays typically form well-ordered face-to-face stacks. Moreover, in biwettable sub-2 µm clay aggregates, <200 nm clay platelets often cover the surfaces of ~1–2 µm sized mineral particles, whereas similarly sized mineral particles in hydrophilic sub-2 µm clay aggregates, in contrast, generally have exposed surfaces without clay platelet coverage. These biwettable vs. hydrophilic behaviors are attributed to a difference in the surface characteristics of the <200 nm clay platelets caused by toluene-unextractable organic carbon coatings. Nanometer-scale carbon mapping reveals an inhomogeneous toluene-unextractable organic carbon coating on the surfaces of <200 nm platelets in biwettable clays. In contrast, hydrophilic clays have a significantly lower amount of toluene-unextractable organic carbon, which tends to be concentrated at steps or near metal oxide nanoparticles on clay particle surfaces. Mixing surface-active organic species, such as asphaltene, resin, or carboxylic organic acids of various types with inorganic solids can lead to a dramatically enhanced emulsion stability. Consequently, understanding the origin and characteristics of sub-2 µm clay solids in bitumen froth is important to (i) clarify their potential role in the formation of stable water-in-oil emulsions during bitumen production and (ii) improve froth treatment process performance to further reduce contaminant solids in solvent-diluted bitumen products. We discuss the implications of our results from these two perspectives.


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