Surface soil-pH map of Queensland

Soil Research ◽  
1994 ◽  
Vol 32 (2) ◽  
pp. 212 ◽  
Author(s):  
CR Ahern ◽  
MMG Weinand ◽  
RF Isbell

Surface soil pH can influence biological activity, nutrition and various chemical processes in the soil. Low pH or acidity is causing major concern in southern Australia, prompting requests for details on the extent, severity and distribution of acidic soils in Queensland. By creating a soil pH database, using an appropriate base map, rainfall isohyets and GIS technology, a coloured pH map of surface soils was produced at a 1:5000000 scale for the entire State. As most samples were from virgin or little disturbed sites, the map generally reflects naturally occurring soil pH. Developed horticultural, agricultural and fertilized pastoral areas are likely to have lower pH than that mapped. About two thirds (63.1%) of Queensland's soils have acidic surfaces, 9.5% neutral and the remaining 26.9% are alkaline. The major proportion (74%) of the > 1200 mm rainfall zone is strongly acid, and the remainder is medium acid or acid. Much of the sugar growing areas occur in this zone. Surface soil pH generally decreases as rainfall increases and to a lesser extent from subtropical to tropical climate. In addition to climate, identification of the soil type assists with predicting pH, as the organic, coarse and medium textured soils and massive earths are more likely to be acid and have low buffering capacity. Depending on the land use, such soils may require regular liming or minimizing of net acidifying practices for long term sustainability.


1982 ◽  
Vol 62 (3) ◽  
pp. 695-702 ◽  
Author(s):  
G. H. NEILSEN ◽  
P. B. HOYT ◽  
O. L. LAU

’Starkrimson’ Delicious (Malus domestica Borkh.), 10–15 yr old, on seedling rootstock, were sampled in several orchards, selected for uniformly low soil pH (< 5.0), medium pH and high pH (6.5–7.3). Harrold Red Delicious, 20–25 yr old, were sampled in 18 orchards which had low, medium and high pH within each. Soils with low pH were generally characterized by higher exchangeable Mn and lower exchangeable Ca. Exchangeable soil Mg and K levels were not significantly related to soil pH. On soils of low pH, higher leaf Mn was the main plant nutrient response with both Harrold Red and Starkrimson trees. Significantly decreased leaf Ca was observed on the younger Starkrimson trees at low soil pH. Soil pH had no direct effect on fruit firmness, soluble solids, juice acidity, or flesh Ca, Mg and K contents. Poststorage fruit quality problems were primarily surface scald and were not related to differences in soil pH. Incidence of flesh browning was, however, related to low flesh Ca content.



1990 ◽  
Vol 30 (5) ◽  
pp. 637 ◽  
Author(s):  
PJ Dolling ◽  
WM Porter ◽  
AD Robson

Thirty-eight sites on acid soils (pH<5.5, 1:5 in water) in the medium rainfall region of Western Australia were sampled to examine spatial variation in soil pH and 0.01 mol/L CaCl2-extractable aluminium. We also examined the relationship between (i) the A1 and A2 horizon soil pH, (ii) the A1 and A2 horizon extractable aluminium, (iii) surface and subsurface soil pH and (iv) surface soil and subsurface soil-extractable Al. Soil at each site generally had a light-textured layer overlying a clay layer at varying depths (30-70 cm) and was classified as either Dy 5.21 or Dy 5.41 (Northcote 1979). Over 80% of the sites had surface soil pH values 4.8 or lower and extractable aluminium concentrations 2 �g/g or higher. There was a very poor correlation (r2 = 0.21) between the A1 horizon soil aluminium extracted in 0.01 mol/L CaCl2 and the pH measured in 0.01 mol/L CaCl2 over 1 ha sites. The relationship was slightly improved in the A2 horizon (r2 = 0.49). The coefficients of variation of soil pH varied from 1.2 to 5.1%, while the coefficients of variation for CaCl2-extractable aluminium varied from 10 to 50%. At many of the sites, low pH values and high aluminium concentrations extended down to 35-45 cm. At the B horizon the pH values generally increased and the aluminium concentrations decreased. The surface soil pH and extractable aluminium were not good indicators (r2 = 0.09-0.60) of the subsurface soil pH and extractable aluminium.



2001 ◽  
Vol 33 (1) ◽  
pp. 75-82 ◽  
Author(s):  
K. I. Paul ◽  
A. S. Black ◽  
M. K. Conyers


1967 ◽  
Vol 47 (3) ◽  
pp. 203-210 ◽  
Author(s):  
L. B. MacLeod ◽  
L. P. Jackson

The concentration of water-soluble and exchangeable aluminum was determined in the 0–15-, 15–23-, 23–30- and 30–45-cm depths of a Podzol limed to provide surface soil pH values ranging from 4.5 to 7.2. Both soluble and exchangeable Al decreased with increasing soil pH. Soluble Al ranged from 5.7 ppm at pH 4.4 with high fertilization to 0.3 ppm at pH 6.5 with similar fertilization. Increasing the rate of fertilization at pH 4.5 raised the soluble Al from 2.6 to 5.7 ppm. Fertilization still doubled the soluble Al in soil at pH 5.1 but had little effect as the pH was raised further to 5.8 and 6.5. Soluble Al in the subsoil samples was less than in surface soil samples at the same pH, while with exchangeable Al, the concentration was greater in the subsoil than in the surface soil samples.There was not a direct relationship between pH and soluble Al, although the highest soluble Al concentrations occurred at lowest soil pH levels. Analyses of 30 representative samples of surface soil taken from farmers' fields showed that the soluble Al concentration at pH 4.0 ranged from 3.5 to 4.8 ppm, while at a pH of 5.0 it ranged from 0.2 to 2.8 ppm. The concentrations of soluble Al in many of these soils exceeded the levels previously shown by nutrient solution experiments to severely restrict growth of legumes and some varieties of barley.



Soil Research ◽  
1991 ◽  
Vol 29 (4) ◽  
pp. 483 ◽  
Author(s):  
RL Aitken ◽  
PW Moody

Ninety soil samples (81 surface, 9 subsurface) were collected from eastern Queensland and soil pH (1:5 soi1:solution) was measured in each of deionized water (pH,), 0.01 M CaCl2, 0-002 M CaCl2 and 1 M KCl. Soil solution was extracted from each soil after incubation for 4 days at the 10 kPa matric suction moisture content, and pH (pHss) and electrical conductivity were measured. The objectives of this work were to investigate interrelationships between soil pH measurements in various electrolytes and soil solution pH in a suite of predominantly acidic soils. Although the relationships between pHw and pH measured in the other electrolytes could be described by linear regression, the fitting of quadratic equations improved the coefficients of determination, indicating the relationships were curvilinear. The majority of soils exhibited variable charge characteristics (CEC increases with soil pH) and the curvilinear trend is explained on this basis. At low pH, the difference between pH, and pH measured in an electrolyte will be small compared with the difference at higher pH values because, in general, at low pH, soils will be closer to their respective PZSE (pH at which electrolyte strength has no effect). Of the electrolytes used, pH measured in 0.002 M CaCl2 gave the closest approximation to pHs,. However, when soils with ionic strengths greater than 0.018 M were selected (predominantly cultivated surface soils), pH in 0.01 M CaCl2 gave the best approximation to pHss. For predicting pHss, the ionic strength of the electrolyte will need to be matched to that of the soils studied. For a suite of soils with a large range in soil solution ionic strength (as in this study), it is preferable to measure pHss directly.



2007 ◽  
Vol 47 (8) ◽  
pp. 949 ◽  
Author(s):  
B. J. Scott ◽  
I. G. Fenton ◽  
A. G. Fanning ◽  
W. G. Schumann ◽  
L. J. C. Castleman

This study, in southern New South Wales (NSW), examined the chemical properties of ~4700 surface soils in agricultural paddocks and recorded lime and gypsum inputs. The area was bounded approximately by Cootamundra in the north, the NSW/Victorian border in the south, extending to Tumbarumba in the east and to near Berrigan in the west. The long-term average annual rainfall ranged from ~420 mm in the west to a maximum of 1175 mm in the east. The data, collected between 1997 and 2003, were for the surface 20 cm of soil, in two 10-cm layers. The data were generated from a soil testing program conducted with farmers in the region. We grouped the soils into three zones based on a GPS location taken at the time of sampling. These zones were 1 (lower rainfall mixed farming), 2 (higher rainfall mixed farming) and 3 (long-term pasture). Acidic soils occurred across all three zones; however, the soils in zone 1 appeared to be less acidic than soils in the other two zones. We found that surface soils (0–10 cm) with soil pH in 1 : 5 soil : 0.01 mol/L calcium chloride (pHCa) ≤4.5 represented 27%, 57% and 54% for zones 1, 2 and 3, respectively. In addition, zone 1 had 74% of surface soils with a pHCa ≤ 5.0, and this was more acidic than previously reported. However, the surface soils in zone 1 had relatively low exchangeable aluminium (Alex) and had less acidic subsurface soils (10–20 cm), so that responses to lime application by pastures and crops may be less frequent or smaller than the surface soil pHCa alone may indicate. There was a higher frequency of acidic soils (pHCa ≤ 4.5) in the subsurface soils than in the surface soils in zones 2 (62 cf. 57%) and 3 (64 cf. 54%), suggesting that the acidity problem at this depth was a major problem. Low pHCa in the subsurface soil is known to be a constraint on crop yield. We found no evidence of the amendment of this soil depth when lime was applied and incorporated into the 0–10 cm depth, and economic amendment of acidity in the 10–20 cm depth remains unresolved. Increased adoption of liming occurred in the late 1990s, and by 1997 the percentage of paddocks limed was 14.3%, 21.3% and 13.6% in zones 1 to 3, respectively. Soil pH buffering and long-term pHCa decline after liming were similar to rates reported in field experiments. The total quantities of lime applied were insufficient for soil amendment and maintenance of soil pHCa, particularly in the long-term pasture areas. The rate of soil acidification in the 0–20 cm depth in the average annual rainfall range of 525–625 mm was estimated to be 1.52 kmol H+/ha.year. This would require 76 kg lime/ha.year to neutralise. Sodic and saline soils occurred mainly in the lower rainfall cropping areas, and were more frequent in an area around the township of Lockhart. Half the gypsum applications were at low rates (≤0.5 t/ha), and were probably for sulfur application to canola. Some of the sodic soils were acidic (34% ≤ pHCa 4.5) so that the application of lime/gypsum mixes could be appropriate in the amendment of these soils. Soils in the pasture system had mean organic carbon content (OC%) of 2.42, compared to the cropping zones at 1.65 and 1.75%. OC% was related to annual average rainfall; the increase in OC% was 0.19% and 0.08% for each 100 mm of average annual rainfall for the surface and subsurface soil, respectively. A group of soils in the cropping areas had surface OC% ≤ 1.25% OC (zone 1, 12%; zone 2, 20%) and this could be the result of intensive cropping. Most soils (55–63%) were of moderate P status (P(Colwell), 21–60 µg/g). However, there was still a substantial group of soils (31–43%) of low P status (P ≤ 20 µg/g). Most surface soils in all zones (72–80%) were low to marginal in sulfur status (KCl 40, ≤10 mg S/kg). Sulfur deficiency has been identified in canola, and current practice in the cropping areas is for inputs of gypsum at low rates.



1996 ◽  
Vol 47 (1) ◽  
pp. 109 ◽  
Author(s):  
RL Aitken ◽  
RA Stephenson ◽  
PW Moody ◽  
EC Gallagher

The chemical properties of the soil at depths of 0-5, 5-10, 10-20, 20-30 and 30-50 cm at two field sites with established macadamia trees were monitored for 5 years following the surface application of various rates of lime (0-1200 g/m2). The effects of annual applications of N and N plus lime were also studied at one site. Both sites received >I700 mm annual rainfall and had strongly acidic, sandy soils. A residual effect of increased pH in the surface soil (0-5 cm depth) was evident after 5 years for lime rates 2200 g/m2. Differences in the nature of the residual effect at each site are discussed in relation to soil acidification, lime dissolution and leaching. High lime rates (>300 g/m2) applied to the soil surface increased pH and reduced extractable A1 in the 10-20 cm depth interval after 12 months. Three years after application, the soil pH at depths of 20-30 and 30-50 cm had been significantly (P < 0.05) increased by surface applications of 600 and 1200 g lime/m2, respectively. The results of this study show that surface application of lime at economic rates (300 to 600 g/m2) can reduce subsoil acidity in coarse-textured soils in high rainfall areas.



Soil Research ◽  
1992 ◽  
Vol 30 (2) ◽  
pp. 169 ◽  
Author(s):  
WJ Slattery ◽  
VF Burnett

Soil pH measured in 0.01 M CaCl2 was found to increase by up to 0.23 of a unit due to long term (7 years) storage of dried surface soil. In comparison, pH measured in water was found to increase by up to 0.55 of a unit after the same time of storage. Soils with the highest ionic strength were found to have the largest pH change. There appeared to be no relationship between soil type and pH change due to storage of soils. We suggest that caution be exercised when re-analysing soils that have been stored for long periods, for water and CaCl2 pH.



1982 ◽  
Vol 62 (1) ◽  
pp. 155-163 ◽  
Author(s):  
P. B. HOYT ◽  
A. M. F. HENNIG

Acidification of two soils was measured in an experiment in which fertilizer and CaCO3 treatments were applied in various combinations. The highest rate of fertilizer used, which included N at 139 kg/ha, decreased the pH in 4–5 yr in unlimed Donnelly (Gray Luvisol) and Josephine (Eluviated Gleysol) soils by 0.43 and 0.18 units, respectively. The fertilizer increased the soluble Al content in both soils. Yields of barley (Hordeum vulgare L.) were greatly increased by the fertilizer and lime treatments. However, by the fourth crop on the Josephine soil, fertilizer failed to give a yield increase in the absence of lime; this was apparently due to declining soil pH and increasing soluble Al. In another experiment, loss of lime was measured over an 8-yr period in six soils that had been limed with Ca(OH)2 to pH 6.5–7.0. The average loss of lime from the soils was equivalent to 495 kg of CaCO3/ha annually. This was accompanied by a decline in pH of 0.48 unit in the 8 yr. Liming caused substantial increases to subsoil pH for three of the soils. Despite the decline in surface soil pH, increases in yields of barley from liming were sustained over the 8-yr period. The implication of these findings to soil fertility practices in the Peace River region are discussed.



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