Phosphate desorption from the surface of soil mineral particles by a phosphate-solubilizing fungus

2012 ◽  
Vol 49 (4) ◽  
pp. 481-486 ◽  
Author(s):  
Nelson Walter Osorio ◽  
Mitiku Habte
1996 ◽  
Vol 34 (7-8) ◽  
pp. 259-265 ◽  
Author(s):  
Marija Kastelan-Macan ◽  
Mira Petrovic

The competitive sorption of phosphates and marine fulvic acids on mineral particles (sand, calcite, bentonite and hematite) has been studied under simulated estuarine conditions. Afterwards, the release and desorption of bound phosphates by solutions containing dissolved fulvic acids was determined. It was found out that due to the favorable sorption of fulvic acids onto minerals studied binding of phosphate was significantly decreased. Desorption experiments showed that fulvic acids, present at high concentration level, similar to that in interstitial water of an oxygenated sediment, increase phosphate desorption by 10-20%.


2017 ◽  
Vol 14 (5) ◽  
pp. 1153-1164 ◽  
Author(s):  
Xiaoqian Jiang ◽  
Roland Bol ◽  
Barbara J. Cade-Menun ◽  
Volker Nischwitz ◽  
Sabine Willbold ◽  
...  

Abstract. Phosphorus (P) species in colloidal and dissolved soil fractions may have different distributions. To understand which P species are potentially involved, we obtained water extracts from the surface soils of a gradient from Cambisol, Stagnic Cambisol to Stagnosol from temperate grassland in Germany. These were filtered to  <  450 nm, and divided into three procedurally defined fractions: small-sized colloids (20–450 nm), nano-sized colloids (1–20 nm), and dissolved P (<  1 nm), using asymmetric flow field-flow fractionation (AF4), as well as filtration for solution 31P-nuclear magnetic resonance (NMR) spectroscopy. The total P of soil water extracts increased in the order Cambisol  <  Stagnic Cambisol  <  Stagnosol due to increasing contributions from the dissolved P fraction. Associations of C–Fe/Al–PO43−/pyrophosphate were absent in nano-sized (1–20 nm) colloids from the Cambisol but not in the Stagnosol. The 31P-NMR results indicated that this was accompanied by elevated portions of organic P in the order Cambisol  >  Stagnic Cambisol  >  Stagnosol. Across all soil types, elevated proportions of inositol hexakisphosphate (IHP) species (e.g., myo-, scyllo- and D-chiro-IHP) were associated with soil mineral particles (i.e., bulk soil and small-sized soil colloids), whereas other orthophosphate monoesters and phosphonates were found in the dissolved P fraction. We conclude that P species composition varies among colloidal and dissolved soil fractions after characterization using advanced techniques, i.e., AF4 and NMR. Furthermore, stagnic properties affect P speciation and availability by potentially releasing dissolved inorganic and ester-bound P forms as well as nano-sized organic matter–Fe/Al–P colloids.


2016 ◽  
Author(s):  
Xiaoqian Jiang ◽  
Roland Bol ◽  
Barbara J. Cade-Menun ◽  
Volker Nischwitz ◽  
Sabine Willbold ◽  
...  

Abstract. Stagnant water conditions may release phosphorus (P) in soil solution that was formerly bound to Fe oxides. To understand which P species are potentially involved, we obtained water extracts from the surface soils of a gradient from Cambisol, Stagnic Cambisol to Stagnosol from temperate grassland, Germany. These were filtered to Stagnosol. Across all soil types, elevated proportions of inositol hexakisphosphate species (e.g. myo-, scyllo-, and D-chiro-IHP) were associated with soil mineral particles (i.e. bulk soil and small-sized soil colloids) whereas other orthophosphate monoesters and phosphonates were found in the ‘dissolved’ P fraction. We conclude that stagnic properties affect P speciation and availability by potentially releasing dissolved inorganic and ester-bound P forms as well as nano-sized organic matter-Fe/Al-P colloids.


Minerals ◽  
2021 ◽  
Vol 11 (9) ◽  
pp. 913
Author(s):  
Jinbang Zhai ◽  
Ze Zhang ◽  
Andrey Melnikov ◽  
Mingyi Zhang ◽  
Linzhen Yang ◽  
...  

The freeze–thaw cycle can change the size and shape of soil particles, that is, cause fragmentation and aggregation of soil mineral particles, thereby affecting the soil structure, which, in turn, affects the soil properties. In addition, the process of soil mineral fragmentation and aggregation, as an event closely related to the cold climate, plays an irreplaceable role in reconstructing the climatic conditions of a certain area and a certain period of time and has important referential significance for the restoration of historical permafrost boundaries and the study of climate change. Therefore, in order to better study the effect of freeze–thaw cycles on the fragmentation and aggregation of soil mineral particles, four soil specimens were selected for this study; the freeze–thaw cycle tests were carried out 0, 3, 6, 9, 50, and 100 times, respectively, and the test results were analyzed. The results of these experiments indicate that (1) after freeze–thaw cycles, the changes in grain-size distribution are different in various soil types, and the changes are mainly concentrated in 0.001–0.1 mm; (2) the coarse particle size particles (sand, silt) can be fragmented into relatively fine-grained particles (silt, clay). The fine-grained particles (clay) cannot undergo fragmentation, and the decrease in clay is due to its aggregation; (3) with the increase in freeze–thaw cycles, the fraction change trend of four specimens is parallel to the x-axis, which means the fragmentation and aggregation of soil mineral particles are in a state of equilibrium or balance; (4) the increase in the Kvar value indicates the change in grain-size distribution, which means aggregation and fragmentation of soil mineral particles. After the 100th cycle, the Kvar value of four specimens is <0.1, which belongs to a low-intensity area; (5) the freeze–thaw cycle will change the type of soil, and after 100 freeze–thaw cycles, the soil type of specimen (H) changes from silty clay loam to silty clay; (6) during the freeze–thaw process, different types of soil have different situations of aggregation and fragmentation.


Author(s):  
G. M. Brown ◽  
D. F. Brown ◽  
J. H. Butler

The term “gel”, in the jargon of the plastics film industry, may refer to any inclusion that produces a visible artifact in a polymeric film. Although they can occur in any plastic product, gels are a principle concern in films where they detract from the cosmetic appearance of the product and may compromise its mechanical strength by acting as local stress concentrators. Many film gels are small spheres or ellipsoids less than one millimeter in diameter whereas other gels are fusiform-shaped and may reach several centimeters in length. The actual composition of gel inclusions may vary from miscellaneous inorganics (i.e. glass and mineral particles) and processing additives to heavily oxidized, charred or crosslinked polymer. The most commonly observed gels contain polymer differing from the bulk of the sample in its melt viscosity, density or molecular weight.Polymeric gels are a special concern in polyethylene films. Over the years and with the examination of a variety of these samples three predominant polymeric species have been observed: density gels which have different crystallinity than the film; melt-index gels in which the molecular weight is different than the film and crosslinked gels which are comprised of crosslinked polyethylene.


Author(s):  
Karen A. Katrinak ◽  
James R. Anderson ◽  
Peter R. Buseck

Aerosol samples were collected in Phoenix, Arizona on eleven dates between July 1989 and April 1990. Elemental compositions were determined for approximately 1000 particles per sample using an electron microprobe with an energy-dispersive x-ray spectrometer. Fine-fraction samples (particle cut size of 1 to 2 μm) were analyzed for each date; coarse-fraction samples were also analyzed for four of the dates.The data were reduced using multivariate statistical methods. Cluster analysis was first used to define 35 particle types. 81% of all fine-fraction particles and 84% of the coarse-fraction particles were assigned to these types, which include mineral, metal-rich, sulfur-rich, and salt categories. "Zero-count" particles, consisting entirely of elements lighter than Na, constitute an additional category and dominate the fine fraction, reflecting the importance of anthropogenic air pollutants such as those emitted by motor vehicles. Si- and Ca-rich mineral particles dominate the coarse fraction and are also numerous in the fine fraction.


Sign in / Sign up

Export Citation Format

Share Document