scholarly journals Organic acids promote phosphorus release from Mollisols with different organic matter contents

2020 ◽  
Vol 16 (No. 1) ◽  
pp. 59-66
Author(s):  
Xiaoyan Yang ◽  
Chuandong Zhang ◽  
Haiping Gu ◽  
Xiangwei Chen ◽  
Erhui Guo
Keyword(s):  
Organic Matter ◽  
Soil Organic Matter ◽  
Organic Acids ◽  
Inorganic Phosphorus ◽  
Phosphorus Release ◽  
Chemical Fractionation ◽  
P Availability ◽  
Inorganic P ◽  
Soil P ◽  
Fractionation Method

Organic acids could improve the phosphorus (P) availability through enhancing the release of inorganic phosphorus (P<sub>i</sub>) in the soil. However, the effects of organic acids on the P<sub>i</sub> release are still poorly understood, especially from soils with different organic matter contents. Here, a biochemically produced humic acid and P fertiliser were added to the soil to modify the content of the soil organic matter (SOM) and soil P, respectively. And then the soil samples were incubated at 25 °C for 30 days. The release of P<sub>i</sub> fractions (such as H<sub>2</sub>O-P<sub>i</sub>, NaHCO<sub>3</sub>-P<sub>i</sub>, NaOH-P<sub>i</sub>, HCl-P<sub>i</sub>, and Residual-P) from the soils with different organic matter contents in the presence of citric, oxalic, and malic acids was evaluated using a sequential chemical fractionation method. The results showed that the release of the NaHCO<sub>3</sub>-P<sub>i</sub>, NaOH-P<sub>i</sub>, and HCl-P<sub>i</sub> fractions also showed a decreasing trend with an increasing content of soil organic matter, and more NaOH-P<sub>i</sub> than the other P<sub>i</sub> fractions was generally released in the presence of organic acids. Considering the types of organic acids, oxalic acid and malic acid most effectively and least effectively released P<sub>i</sub>, respectively. The path analysis indicated that the NaOH-P<sub>i</sub> release had the highest direct and indirect effects on the total inorganic P (TP<sub>i</sub>) release. NaOH-P<sub>i</sub> was, therefore, the most effective source of P<sub>i</sub> in the Mollisols.

Indicators of forest ecosystem productivity and nutrient status across precipitation and temperature gradients in Hawaii

2007 ◽  
Vol 23 (6) ◽  
pp. 693-704 ◽  
Author(s):  
Travis Idol ◽  
Patrick J. Baker ◽  
Dean Meason
Keyword(s):  
Organic Matter ◽  
Soil Organic Matter ◽  
Basal Area ◽  
Forest Productivity ◽  
P Availability ◽  
Soil P ◽  
Leaf Nutrients ◽  
Soil P Availability ◽  
P Fraction ◽  
Leaf N

Precipitation and temperature are known to have important effects on forest productivity, but these effects may be strongly mediated through their influence on soil and leaf nutrients. We measured indicators of forest productivity and soil and leaf nutrients across independent gradients of precipitation and elevation/temperature in lower montane Hawaiian forests dominated by a single overstorey species, Acacia koa, situated on 1500–3000-y-old soils that were mixtures of volcanic ash and basalt. Stand basal area was highest at the wettest site, 2000 mm mean annual precipitation (MAP), and leaf N and P were lowest at the driest site, 1000 mm MAP. Soil N availability and leaf N concentration declined across an 850-m elevation gradient, but this was not correlated with stand basal area or soil organic matter content. Across all stands, basal area was negatively correlated with the exchangeable soil P fraction. As well, the soil C:N ratio was negatively correlated with both soil P availability and the size of the primary mineral P fraction. Soil P availability and weathering appear to be important determinants of soil organic matter quantity and quality. Overall, precipitation is the major driving force for forest productivity, but P weathering and availability play important roles in limiting productivity in wetter sites and in controlling soil organic matter dynamics in these N-fixing forests.

DISTRIBUTION OF ORGANIC MATTER AND PHOSPHORUS FRACTIONS IN A TOPOGRAPHIC SEQUENCE OF SOILS IN SOUTHERN BRITISH COLUMBIA

1965 ◽  
Vol 45 (3) ◽  
pp. 323-329 ◽  
Author(s):  
M. J. S. Floate
Keyword(s):  
British Columbia ◽  
Organic Matter ◽  
Soil Organic Matter ◽  
Organic Phosphorus ◽  
Inorganic Phosphorus ◽  
Similar Amount ◽  
Grassland Soils ◽  
Inorganic P ◽  
Parent Materials ◽  
C And N

In sequences of grassland soils on south-facing slopes and forested soils on north-facing slopes in southern British Columbia, pH decreased but C, N, and organic phosphorus (Po) increased with increase in elevation from 1800 to 7400 ft. At the highest elevations grassland and forested soils contained similar amounts of C, N, and Po. The surface horizons of grassland soils at the lowest elevations contained C and N in similar amount to forested soils between 4000 and 5000 ft. C, N, and Po decreased with depth in all profiles but the amount of H2SO4-soluble inorganic P (Pa) increased to its highest percentage of the total, up to 98%, in the parent materials. Although both C/N and C/Po ratios decreased with depth, the values for C/Po were not high and indicated that inorganic phosphorus supply is not limiting the accumulation of P in the soil organic matter. These properties were interpreted as the effects of climate, modified by elevation, aspect, and vegetation, on weakly weathered parent materials.

scholarly journals Soil organic matter as a function of nitrogen fertilization in crop successions

2005 ◽  
Vol 62 (4) ◽  
pp. 374-380 ◽  
Author(s):  
Renato Yagi ◽  
Manoel Evaristo Ferreira ◽  
Mara Cristina Pessôa da Cruz ◽  
José Carlos Barbosa ◽  
Luiz Alberto Navarro de Araújo
Keyword(s):  
Organic Matter ◽  
Soil Organic Matter ◽  
Nitrogen Fertilization ◽  
Fulvic Acids ◽  
Water Soluble ◽  
Chemical Fractionation ◽  
Organic C ◽  
Fractionation Method ◽  
C And N ◽  
N Rates

The interdependence between the C and N cycles is reflected by the levels of soil organic matter (SOM). SOM and organic C levels in water soluble (C-WS) humic acids (C-HA), fulvic acids (C-FA), and humin fractions (C-H) were evaluated through the classic chemical fractionation method in samples of a Rhodic Eutrudox from a randomized blocks experimental design, with split-split-plots using five nitrogen sidedressing levels for corn (0; 60; 120; 180; and 240 kg ha-1 N) as the main treatment, two crop sequences (corn-corn and soybean-corn) as the secondary treatment, and two sampling depths (0 to 0.2 and 0.2 to 0.4 m) as a sub-subtreatment. Nitrogen fertilization did not affect SOM levels, but favored the synthesis of substances in the C-HA fraction. There was a quadratic effect of N rates on the C-WS and C-FA levels in the corn-corn succession. The soybean-corn succession resulted in larger SOM and organic C levels in the C-H fraction.

Relationship between phosphorus fractions and properties of highly calcareous soils

Soil Research ◽  
2007 ◽  
Vol 45 (4) ◽  
pp. 255 ◽  
Author(s):  
Ebrahim Adhami ◽  
Hamid Reza Memarian ◽  
Farzad Rassaei ◽  
Ehsan Mahdavi ◽  
Manouchehr Maftoun ◽  
...  
Keyword(s):  
Calcareous Soils ◽  
Hydroxylamine Hydrochloride ◽  
Inorganic Phosphorus ◽  
Influential Factor ◽  
Sequential Fractionation ◽  
Inorganic P ◽  
Soil P ◽  
Fractionation Procedure ◽  
Extractable P ◽  
P Content

Inorganic phosphorus (P) sequential fractionation schemes are applicable techniques to interpret soil P status. The present study was initiated to determine the origin of various P fractions in highly calcareous soils. Inorganic P forms were determined by a sequential fractionation procedure extracting with NaOH (NaOH-P), Na citrate-bicarbonate (CB-P), Na citrate 2 times (C1-P and C2-P), Na citrate-ascorbate (CAs-P), Na citrate-bicarbonate-dithionite (CBD-P), Na acetate (NaAc-P), and HCl (HCl-P). Results showed that NaOH-P was negatively correlated with active iron oxides. CB-P was positively correlated with silt content and negatively related to citrate-bicarbonate-dithionite extractable Fe (Fed). This result illustrates the weathering effect on Ca-P, with Ca-P content declining as a consequence of weathering. A negative correlation was observed between C1-P and citrate ascorbate extractable Fe (FeCAs). Second citrate extractable P (C2-P) was negatively related to calcium carbonate equivalent and positively related to hydroxylamine-hydrochloride and neutral ammonium acetate-hydroquinone extractable Mn (Mnh and Mnq). Fine silt (Fsilt) was the most influential factor affecting CAs-P. It seemed citrate-dithionite-bicarbonate extractable Al (Ald), Mnh, and Mnq have been sinks for CBD-P, while free iron oxide compounds (Feo, Fec, and FeCAs) were a major contributing factor for the formation of NaAc-P. Stable P compounds (HCl-P) of highly calcareous soils originated from coarse silt (Csilt) and hydroxylamine-hydrochloride extractable Mn (Mnh).

scholarly journals Short-term effects of phosphate fertilizer enriched with low molecular weight organic acids on phosphorus release kinetic and availability under calcareous conditions in arid region

2018 ◽  
Vol 2 ◽  
pp. 66
Author(s):  
Adil Mihoub ◽  
Mustapha Daddi Bouhoun ◽  
Asif Naeem
Keyword(s):  
Molecular Weight ◽  
Acid Solution ◽  
Organic Acids ◽  
Phosphorus Release ◽  
Favorable Effect ◽  
Available Phosphorus ◽  
Low Molecular Weight ◽  
Release Kinetic ◽  
P Availability ◽  
Phosphate Fertilizers

Phosphate reactions and retention in the soil are of paramount importance from the perspective of plant nutrition and fertilizer use efficiency. The objective of this work was to investigate the effect of some low molecular weight organic acids (LMWOAs) on phosphorus release kinetic and its availability in calcareous soil. Experiments were conducted in laboratory. Soil-limestone mixtures were prepared to achieve highly calcareous samples (i.e. 50% CaCO3). The prepared samples were mixed thoroughly with phosphate fertilizers i.e. Triple super phosphate (TSP) and Monoammonium Phosphate (MAP) and watered with distilled water only (CK), with citric acid solution (CA) and with oxalic acid solution (OA). The treatments were arranged in a CRD with three replications and incubated at 25 ± 2°C and 80% soil moisture for a period of 960 h. The parabolic model was used for describing the decrease in P with time. As a result, all treatments showed a significant decrease in available P with time. Using LMWOAs showed important results and combination of phosphate fertilizers with both LMWOAs solutions exerted a very favorable effect on P availability in soil. The parabolic diffusion equation used was fitted well to experimental data. Addition of LMWOAs decreased loss in extractability of P with increasing soil available phosphorus fraction. Moreover, treatments irrigated by LMWOAs solutions released a lot of phosphorus compared to untreated treatments.

Rate of recycling of sulfur from urine, feces and litter applied to the soil surface

Soil Research ◽  
1994 ◽  
Vol 32 (3) ◽  
pp. 543 ◽  
Author(s):  
GJ Blair ◽  
AR Till ◽  
C Boswell
Keyword(s):  
Organic Matter ◽  
Soil Organic Matter ◽  
Soil Surface ◽  
Plant Litter ◽  
Test Plant ◽  
Soil P ◽  
S Uptake ◽  
Organic Matter Pool ◽  
Preferential Uptake ◽  
Soil Organic Matter Pool

The recycling of S from plant litter, dung and urine is an important process for supplying S for pastures. A pot experiment was conducted where 35S-labelled litter (25% white clover/38% ryegrass/21% weed) and S-35-labelled urine and faeces collected from sheep fed the same herbage as was used as litter was surface applied to pots and the fate of the applied S was followed for 100 days with ryegrass as the test plant. In camp soil, 45% of the S applied in urine was taken up by ryegrass plants within 12 days of application. In non-camp soil, the uptake of urine-S was about 20% over the same period. Cumulative uptake of 35S from urine in camp soil was subsequently restricted, with a maximum of 60% eventually measured in plants after 100 days. Mean rates of release of S (0-37 days) from litter and faeces was respectively 16.2 and 4.5 mg g-1 day-1. The calculated half-times from S in the two materials were respectively 43 and 154 days under controlled environmental conditions with adequate moisture. Litter S followed organic matter (OM) decomposition, but faecal S release was initially more rapid than faecal OM decomposition. There was little S release from faeces after day 25. Rather, S was immobilized in faeces during the 25-100 day period. The decomposition of litter and faeces was divided into an initial rapid process during which soluble S and more labile S was released, followed by a slower process involving the release of S from tissues more resistant to mineralization. The uptake of 35S from labelled materials was initially more rapid than would be expected for total S released from the added litter and faeces and the 35Suptake effect was short-lived relative to the continued effect of added material on total S uptake. The preferential uptake of 35S from the surface-applied material appears to be due to limited root development at the early stages of the experiment. Movement of 35S into the soil organic matter pool was very rapid; 58.4% of urine S was in the soil organic matter fraction in the non-camp soil by day 6. The amount of applied S in the organic matter equilibrated at about day 75. The accumulation of applied S from the materials added was greater than that recorded in previously reported studies for inorganic sulfate (e.g. about 50%). Soil P and S status had little effect on rates of release of S. from the applied materials, however, the effect of the camp and non-camp soil on total S recycling was markedly different as a result of the different amounts of plant growth and thus S uptake in the two soils. The decomposition of litter indicated peak rates of S release at two specific times over the 100 days and indicated successional changes in micro-organism activity. With faeces, the experiment was not continued for sufficiently long to show micro-organism effects.

Dynamics of phosphorus fractions in soils treated with dairy manure

Soil Research ◽  
2020 ◽  
Vol 58 (3) ◽  
pp. 289
Author(s):  
L. B. Braos ◽  
A. C. T. Bettiol ◽  
L. G. Di Santo ◽  
M. E. Ferreira ◽  
M. C. P. Cruz
Keyword(s):  
P Uptake ◽  
Dairy Manure ◽  
P Availability ◽  
Organic P ◽  
Triple Superphosphate ◽  
P Fractions ◽  
Inorganic P ◽  
Soil P ◽  
Plant P Uptake ◽  
Inorganic P Fractions

The evaluation of phosphorus (P) transformations in soil after application of manure or mineral P can improve soil management and optimise P use by plants. The objectives of the present study were to assess organic and inorganic P forms in two soils treated with dairy manure and triple superphosphate and to establish relationships between soil P fraction levels and P availability. Soil organic and inorganic P fractions were quantified using a pot experiment with two soils, a typical Hapludox and an arenic Hapludult, with three types of fertiliser treatments applied (no fertiliser application, application of dairy manure, and application of triple superphosphate, by adding 100 mg P dm–3 in the form of fertiliser in the two latter treatments) and four incubation times (15, 45, 90, and 180 days). Inorganic P was fractionated into aluminium-bound, iron-bound, occluded, and calcium-bound P. Organic P was extracted sequentially using sodium bicarbonate, hydrochloric acid, microbial biomass, sodium hydroxide, and residual organic P. After incubation, maize plants were cropped to quantify dry matter yield and absorbed P. Application of dairy manure resulted in a significant increase in most of the organic P fractions, and application of triple superphosphate led to a significant increase in inorganic P fractions. Both fertilisers raised labile organic P fractions in the two soils. The major sinks of P in Hapludox were occluded and fulvic acid-associated P. In contrast, the major sink of P in Hapludult was iron-bound P. The available P levels were stable after application of dairy manure, and decreased with time when fertilised with triple superphosphate. In the Hapludox, the organic P fractions had a significant positive correlation with P uptake by plants. The results suggest that organic P mineralisation plays a more significant role in plant P uptake in the Hapludox soil and inorganic P forms are the main contributors to plant P uptake in the Hapludult soil.

Phosphorus fractionation in grasses with different resource-acquisition characteristics in natural grasslands of South America

2019 ◽  
Vol 35 (5) ◽  
pp. 203-212 ◽  
Author(s):  
Anderson Cesar Ramos Marques ◽  
Rogério Piccin ◽  
Tales Tiecher ◽  
Leandro Bittencourt de Oliveira ◽  
João Kaminski ◽  
...  
Keyword(s):  
South America ◽  
Phosphorus Fractionation ◽  
Paspalum Notatum ◽  
Chemical Fractionation ◽  
P Availability ◽  
Inorganic P ◽  
Nutrient Demand ◽  
Natural Grasslands ◽  
Low Phosphorus ◽  
Total P

AbstractThe natural grasslands in South America have soils with low phosphorus (P) availability (1.0 to 7.5 mg kg−1), possibly altering the absorption and accumulation of P in grasses. We evaluated the chemical fractionation of P in the leaves of the most important grasses present in these grasslands to better understand the mechanisms involved in the storage of P. The grasses studied were Axonopus affinis and Paspalum notatum (fast tissue cycling and high nutrient demand) and Andropogon lateralis and Aristida laevis (slow tissue cycling and low nutrient demand). They were grown in pots filled with an Ultisol with two levels of P: control, and addition of 50 mg P kg–1. The main P fractions were the inorganic soluble (44%) and P in RNA (26%). Addition of P increased the total P concentration, following the order A. affinis (140%) > P. notatum (116%) > A. lateralis (81%) > A. laevis (21%). In conclusion, the species A. affinis and P. notatum responded to P fertilization with high variation and accumulating P in less-structural chemical forms, such as inorganic P. The species A. lateralis and A. laevis showed low variation in the concentration of P forms, with higher P concentrations in structural forms.

scholarly journals Effects of air-drying and freezing on phosphorus fractions in soils with different organic matter contents

2011 ◽  
Vol 57 (No. 5) ◽  
pp. 228-234 ◽  
Author(s):  
G. Xu ◽  
J.N. Sun ◽  
R.F. Xu ◽  
Y.C. Lv ◽  
H.B. Shao ◽  
...  
Keyword(s):  
Organic Matter ◽  
Surface Waters ◽  
Organic Matter Content ◽  
Phosphorus Fractions ◽  
Climate Change Scenarios ◽  
P Availability ◽  
Organic P ◽  
Air Drying ◽  
Soil P ◽  
Labile P

Little is known about the effects of air-drying and freezing on the transformation of phosphorus (P) fractions in soils. It is important that the way in which soils respond to such perturbations is better understood as there are implications for both P availability and loss to surface waters from soils. In this study, the effects of air-drying and freezing were investigated using two soils, one being a forest soil (FS) high in organic matter and the other being a sterile soil (SS) low in organic matter. Soil P was fractionated using a modified Hedley fractionation method to examine the changes of phosphorus fractions induced by air-drying and freezing. Generally, there were no significant differences of total phosphorus among the three treatments (CV% &lt; 10%). Compared with field moist soils, freezing the soil evoked few changes on phosphorus fractions except that the resin-P increased in FS soil. On the contrary, air-drying significantly changed the distribution of phosphors fractions for both soils: increased the labile-P (especially resin-P) and organic-P (NaHCO<sub>3</sub>-Po, NaOH-Po and Con.HCl-Po) at the expense of NaOH-Pi and occlude-P (Dil.HCl-P and Con.HCl-Pi). Resin-P significantly increased by 31% for SS soil and by 121% for FS soil upon air-drying. The effect of air-drying seemed to be more pronounced in the FS soil with high organic matter content. These results indicated that drying seem to drive the P transformation form occlude-P to labile-P and organic-P and accelerated the weathering of stable P pool. This potentially could be significant for soil P supply to plants and P losses from soils to surface waters under changing patterns of rainfall and temperature as predicted by some climate change scenarios. &nbsp;

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