The influence of pre-treatment,temperature and calcium ions on trace element uptake by an alga (Scenedesmus pannonicus subsp. Berlin) and fungus (Aureobasidium pullulans)

Experiments were carried out in order to obtain information on the uptake characteristics of metals in the algal and fungal components of lichens. The uptake of ¹¹⁵Cd, ⁶⁵Zn, ⁶⁴Cu, ¹⁴⁰La, ¹⁸⁷W and ⁷⁶As in the alga Scenedesmus pannonicus, subsp. Berlin and the fungus Aureobasidium pullulans was determined at pH 7 and 5 respectively, in 4 h experiments varying with respect to temperature and Ca²⁺ solution concentrations. Furthermore, the effects of pre-rinsing the cell suspensions on metal uptake were investigated.Pre-rinsing resulted in decreased uptake of W and As by algae and in increased uptake of all elements measured by fungi, which may be attributed to combined effects of starvation and changing densities.For algae, the uptake rates of As, W, Zn and Cd were markedly increased at the highest temperature employed. For Cu and La hardly any effects of temperature were observed, indicating the absence of metabolically controlled uptake. For fungi, but for As no relation of uptake with temperature could be determined.The presence of Ca²⁺ ions in the solution applied hardly affected the uptake of As but resulted in increased uptake of W by both the algae and the fungi. The effects of Ca²⁺ on the uptake of Cu and La were relatively small, probably due to specific binding sites in the cell walls for Cu and to the supercalcium status of the La-ion.The presence of Ca²⁺ caused decreased uptake of Cd²⁺ and Zn²⁺ by algae, but hardly affected the uptake of Zn²⁺ by fungi.The results indicate component-specific uptake and accumulation behaviour in intact lichens.     

Effects of Cu2+, Pb2+ and Zn2+ on voltage-activated currents in Helix pomatia L. Neurons

Effects of Cu²⁺, Pb²⁺ and Zn²⁺ were studied on voltage-activated Na-, Ca-, and K-currents in snail neurons. It was found that: 1. In normal physiological saline Cu²⁺, Pb²⁺ and Zn²⁺ ions exerted complex changes on the total ionic currents; 2. All three metal ion have depressed the inward Na-currents but with different K _D , moreover Pb ²⁺ increased Na-current at low concentrations (5 M); 3. The inward Ca-current was also reduced. The sequence of the blocking effect of metals was different: Pb>Cu>Zn, however the steady-state inactivation was influenced only by Cu²⁺; 4. Outward currents were decreased in all neurons by Cu²⁺, but the effects of Pb²⁺ and Zn²⁺ were either depression or enhancement in different indentified neurons; 5. The possibility of binding heavy metals to wide variety of membrane proteins and the observed effects on different ionic channels suggest that the metal effect is complex and cannot be taken as a specific one to a single channel type or site of location.     

Adsorption studies and the removal of dissolved metals using pyrolusite as adsorbent

The adsorption of metals from aqueous solutions of Pb²⁺, Zn²⁺ and Mg²⁺ on naturally occurring pyrolusite have been studied. The chemical stability of the pyrolusite has been determined in NaOH, H₂SO₄, HNO₃, HCl, NaCl and NK₄Cl solutions of various concentrations. Adsorption of the metal ions followed the order Pb²⁺>Zn²⁺>Cd²⁺.The maximum adsorption of Pb²⁺ (100%) occurred at pH 7. the relation between the amount of Pb²⁺ adsorbed per unit weight of pyrolusite and the concentration of Pb²⁺ at equilibrium follows the Freundlich adsorption isotherm.The efficiency of pyrolusite has been demonstrated by removing lead from synthetic waste water. 100% and 96% removal of lead have been achieved from synthetic waste water containing 5 mg l^–1 and 120 mg l^–1 of Pb²⁺ respectively at pH 7. The results of these studies suggest that pyrolusite might provide an economical method for the removal of lead from industrial waste water.     

A new <Emphasis Type="Italic">P. putida</Emphasis> instrumental toxicity bioassay

Here, we present a new toxicity bioassay (CO₂-TOX), able to detect toxic or inhibitory compounds in water samples, based on the quantification of Pseudomonas putida KT2440 CO₂ production. The metabolically produced CO₂ was measured continuously and directly in the liquid assay media, with a potentiometric gas electrode. The optimization studies were performed using as a model toxicant 3,5-DCP (3,5-dichlorophenol); later, heavy metals (Pb²⁺, Cu²⁺, or Zn²⁺) and a metalloid (As⁵⁺) were assayed. The response to toxics was evident after 15 min of incubation and at relatively low concentrations (e.g., 1.1 mg/L of 3,5-DCP), showing that the CO₂-TOX bioassay is fast and sensitive. The EC₅₀ values obtained were 4.93, 0.12, 6.05, 32.17, and 37.81 mg/L for 3,5-DCP, Cu²⁺, Zn²⁺, As⁵⁺, and Pb²⁺, respectively, at neutral pH. Additionally, the effect of the pH of the sample and the use of lyophilized bacteria were also analyzed showing that the bioassay can be implemented in different conditions. Moreover, highly turbid samples and samples with very low oxygen levels were measured successfully with the new instrumental bioassay described here. Finally, simulated samples containing 3,5-DCP or a heavy metal mixture were tested using the proposed bioassay and a standard ISO bioassay, showing that our test is more sensible to the phenol but less sensible to the metal mixtures. Therefore, we propose CO₂-TOX as a rapid, sensitive, low-cost, and robust instrumental bioassay that could perform as an industrial wastewater-process monitor among other applications.     

Biosorption kinetics of heavy metals by leaf biomass of Jatropha curcas in single and multi-metal system

Biosorption of Cu²⁺, Zn²⁺, and Cr⁶⁺ from aqueous solutions by leaf biomass of Jatropha curcas was investigated as a function of biomass concentration, initial metal ion concentration, contact time, and pH of the solution systematically. The aim of this study was to optimize biosorption process and find out a suitable kinetic model for the metal removal in single and multi-metal system. The experimental data were analyzed using two sorption kinetic models, viz., pseudo-first- and pseudo-second-order equations, to determine the best fit equation for the biosorption of metal ions Cu²⁺, Zn²⁺, and Cr⁶⁺ onto the leaf biomass of J. curcas in different metal systems. The experimental data fitted well the pseudo-second-order equation and provided the best correlation for the biosorption process. The findings of the present investigation revealed that J. curcas leaf biomass was an eco-friendly and cost-effective biosorbent for the removal of heavy metal ions from wastewater.     

Vehicular stress a cause for heavy metal accumulation and change in physico-chemical characteristics of road side soils in Pahalgam

In an effort to determine vehicular impact on soil quality, soil samples were collected from three different zones (Pahalgam, Batakote, and Chandanwari) in Pahalgam forest ecosystem. Results showed that a significant decrease in moisture content, organic carbon, available nitrogen, and potassium was observed in nearby road side soils. However, pH was observed to be on neutral side and available phosphorus recorded high concentration. The concentration of heavy metals Pb²⁺, Cu²⁺, Zn²⁺, Ni²⁺, and Cd²⁺ estimated was also significantly high. Furthermore, concentration of Pb²⁺ at high vehicular load subzones was observed to be highest (1.168 mg/Kg) followed by Zn²⁺ (0.896 mg/Kg), Ni²⁺ (0.649 mg/Kg), Cu²⁺ (0.415 mg/Kg), and Cd²⁺ (0.079 mg/Kg). An inter-zone analysis revealed that the concentration of the heavy metals (Pb²⁺?>?Ni²⁺?>?Cd²⁺) was observed to follow the trend, Z-I?>?Z-II?>?Z-III. Variation along the temporal gradient and the impact on soil qualities were notably higher in summer. Vehicular pollution to a great extent impacts physico-chemical characteristics and more interestingly adds substantial concentration of heavy metals in soils.     

多元线性回归-分光光度法测定电镀排放废水中重金属

采用多元线性回归-分光光度法进行电镀排放废水中Cr³⁺、Ni²⁺、Zn²⁺的同时测定研究。以4-(2-吡啶偶氮)间苯二酚(PAR)为显色剂,探索了同时测定模拟电镀废水中Cr³⁺、Ni²⁺、Zn²⁺的实验方法,建立多元线性回归模型。根据实际电镀排放废水中Cr³⁺、Ni²⁺、Zn²⁺的质量浓度分布调查结果,设计了测定较低和较高浓度范围2种模型,分别对应不同水质波动程度的电镀企业废水,前者浓度范围设置基本覆盖大多数实际电镀排放废水中Cr³⁺、Ni²⁺、Zn²⁺的浓度,且具有较高精度。测定浓度范围较小模型对应水质波动较小的电镀排放废水,模型中Cr³⁺、Ni²⁺、Zn²⁺的质量浓度分别为0.32～0.44、0.32～0.50、0.72～0.84 mg/L,平均相对误差MR...     

Uptake of metal ions in moss from artificial precipitation

Uptake in Hylocomium splendens and Sphagnum fuscum, of Zn, Cu, Cd, and Pb from artificial solutions of precipitation at ambient concentration levels was investigated. The primary objective was to study to what extent major cations and possibility anions in the precipitation might affect the uptake by competition or possibly by complexing reactions. In addition the effect on metal uptake of pH and temperature was studied. The uptake of Zn and partly Cu was lower from precipitation with a high content of seasalt. With increasing metal concentration an increasing amount of Zn and Cu accumulated in the moss. These observations suggest that cations in the precipitation such as Na⁺ and Mg²⁺ may affect the uptake by competition. Possibly also Cl^- may interfere by complexing reactions. Uptake of Zn and Cd was pH dependent. The uptake of all four metals increased with temperature. The results from this work appear to be significant with respect to the interpreation of data from atmospheric deposition surveys based on moss analysis.     

Lichens as Bioindicators of Atmospheric Heavy Metal Pollution in Singapore

Lichens have been used as bioindicators in various atmospheric pollution assessments in several countries. This study presents the first data on levels of heavy metals (As, Cd, Cu, Ni, Pb, and Zn) in lichens at different locations in Singapore, Southeast Asia. Singapore is a fully industrialised island nation, with a prevailing tropical climate and a population of 4 million people within a confined land area of less than 700 km². The ubiquitous lichen species, Dirinaria picta was collected from six sample sites across Singapore and analysed for heavy metals using inductively coupled plasma mass spectrometry (ICPMS). No significant relationship existed between metal levels in lichen and soil, indicating that accumulated metals in lichen are primarily derived from the atmosphere. Peak concentrations of zinc (83.55 μg g⁻¹), copper (45.13 μg g⁻¹) and lead (16.59 μg g⁻¹) in lichens were found at Sembawang, Jurong and the National University of Singapore campus which are locations associated with heavy petroleum and shipping industries, and road traffic respectively. The mean heavy metal levels of lichen samples in Singapore were found to be at the upper range of values reported in the literature for temperate countries.     

Five-year monitoring study of chemical characteristics of Wet atmospheric precipitation in the southern region of Jordan

Wet atmospheric samples were collected from different locations in the southern region of Jordan during a 5-year period (October 2006 to May 2011). All samples were analyzed for pH, EC, major ions (Ca²⁺, Mg²⁺, Na⁺, K⁺, HCO₃ ^?, Cl^?, NO₃ ^?, and SO₄ ^2?), and trace metals (Fe²⁺, Al³⁺,Cu²⁺, Pb²⁺, and Zn²⁺). The highest ion concentrations were observed during the beginning of the rainfall events because large amounts of dust accumulated in the atmosphere during dry periods and were scavenged by rain. The rainwater in the study area is characterized by low salinity and neutral pH. The major ions found in rainwater followed the order of HCO₃?>?Cl^??>?SO₄ ^2? and Ca²⁺?>?Na⁺ > Mg²⁺ > NH₄ ⁺ > K⁺. Trace metals were identified to be of anthropogenic origin resulting from cement and phosphate mining activities located within the investigated area and from heating activities during the cold period of the year (January to April). The wet precipitation chemistry was analyzed using factor component analysis for possible sources of the measured species. Factor analysis (principal component analysis) was used to assess the relationships between the concentrations of the studied ions and their sources. Factor 1 represents the contribution of ions from local anthropogenic activities, factor 2 represents the contribution of ions from natural sources, and factor 3 suggests biomass burning and anthropogenic source. Overall, the results revealed that rainwater chemistry is strongly influenced by local anthropogenic sources rather than natural and marine sources, which is in a good agreement with the results obtained by other studies conducted in similar sites around the world.     

On-site solid-phase extraction and application to in situ preconcentration of heavy metals in surface water

An on-site solid-phase extraction, consisting of the sorption, the separation and the elution function units, was designed for in situ preconcentration of heavy metals ions. The D401 resin powder was employed as sorbent to capture Pb²⁺, Cu²⁺, Zn²⁺, Cd²⁺, Co²⁺, and Ni²⁺, and then they desorbed with 2 mol/L nitric acid as eluent. Under the optimized conditions, these heavy metals ions in West Lake, Taihu Lake, and Yangtze River of China were captured and then determined by ICP-OES with the recovery of 92.5% to 111.5%. The on-site solid-phase extraction achieved a quick preconcentration of heavy metals to avoid the transport and storage of a large volume water sample. It is suitable for in situ monitoring of water quality in mountains, tablelands or other remote areas.     

Development of baseline (air quality) data in Pakistan

During 2003–2004, SUPARCO, the Pakistan Space and Upper Atmosphere Research Commission has conducted a year long baseline air quality study in country’s major urban areas (Karachi, Lahore, Quetta, Rawalpindi, Islamabad and Peshawar). The objective of this study was to establish baseline levels and behavior of airborne pollutants in urban centers with temporal and spatial parameters. This study reveals that the highest concentrations of CO were observed at Quetta (14 ppm) while other pollutants like SO₂ (52.5 ppb), NO _x (60.75 ppb) and O₃ (50 ppb) were higher at Lahore compared to other urban centers like Karachi, Peshawar etc. The maximum particulate (TSP) and PM10 levels were observed at Lahore (996 ug/m³ and 368 ug/m³ respectively), Quetta (778 ug/m³, 298 ug/m³) and in Karachi (410 ug/m³, 302 ug/m³). In all major cities the highest levels were recorded at major intersections and variations were directly correlated with traffic density. These pollutants showed highest levels in summer and spring while lowest were observed in winter and monsoon. A data bank has been generated for future planning and air pollution impact studies.     

Diversity of epiphytic lichens and metal contents of Parmelia caperata thalli as monitors of air pollution in the town of Pistoia (c Italy)

The results of a biomonitoring survey carried out in the town of Pistoia (central Italy) using the biodiversity of epiphytic lichens and the accumulation of heavy metals in thalli of Parmelia caperata as indicators of air pollution are reported. Compared to previous surveys, the overall situation generally improved, with higher lichen diversity at most stations and lower metal concentrations in P. caperata thalli. However, the general picture according to a calibrated scale of environmental naturality/alteration was substantially negative, with about 87% of the study area classified as `altered' (including the lichen desert) or `semi-altered'. To explain this apparent contradiction, it has been suggested that lichen colonization is determined by declining SO₂ concentrations, while major injuries to lichen communities are caused by the constantly high levels of NO_X. In spite of the low levels of Pb measured in P. caperata thalli, vehicular traffic was excluded as the main source of atmospheric pollution. Domestic heating seems to be the main cause of changes in the diversity of epiphytic lichens in the study area.     

Monitoring of Fogwater Chemistry in the Gulf Coast Urban Industrial Corridor: Baton Rouge (Louisiana)

Seventeen fog events were sampled in Baton Rouge, Louisiana during 2002–2004 as part of characterizing wet deposition by fogwater in the heavily industrialized corridor along the Louisiana Gulf Coast in the United States. These samples were analyzed for chemical characteristics such as pH, conductivity, total organic and inorganic carbon, total metals and the principal ion concentrations. The dominant ionic species in all samples were NH₄⁺, NO₃⁻, Cl⁻ and SO₄²⁻. The pH of the fogwater sampled had a mean value of 6.7 with two cases of acidic pH of 4.7. Rainwater and fogwater pH were similar in this region. The acidity of fogwater was a result of NO₃⁻ but partly offset by high NH₄⁺. The measured gaseous SO₂ accounted for a small percentage of the observed sulfate concentration, indicating additional gas-to-particle conversion of SO₂ to sulfate in fogwater. The gaseous NO_x accounted for most of the dissolved nitrate and nitrite concentration in fogwater. The high chloride concentration was attributable to the degradation of chlorinated organics in the atmosphere. The metal composition was traced directly to soil-derived aerosol precursors in the air. The major metals observed in fogwater were Na, K, Ca, Fe, Al, Mg and Zn. Of these Na, K, Ca and Mg were predominant with mean concentrations > 100 μM. Al, Fe and Zn were present in the samples, at mean concentrations < 100 μM. Small concentrations of Mn (7.8 μM), Cu (2 μM), Pb (0.07 μM) and As (0.32 μM) were also observed in the fogwaters, and these were shown to result from particulates (PM_2.5) in the atmosphere. The contribution to both ions and metals from the marine sources in the Louisiana Gulf Coast was minimal. The concentrations of all principal ionic species and metals in fogwater were 1–2 orders of magnitude larger than in rainwater. Several linear alkane organic compounds were observed in the fogwater, representing the contributions from petroleum products at concentrations far exceeding their aqueous solubility. A pesticide (atrazine) was also observed in fogwater, representing the contribution from the agricultural activities nearby.     

Atmosphic pollutants study of particles ionic species during high wind speed (>7 m s-1) near Taiwan strait in central Taiwan from 2004 to 2005

This study monitored atmospheric pollutants during high wind speed (> 7 m s⁻¹) at two sampling sites: Taichung Harbor (TH) and Wuci traffic (WT) during March 2004 to January 2005 in central Taiwan. The correlation coefficient (R ²) between TSP, PM_2.5, PM_2.5−10 particle concentration vs. wind speed at the TH and WT sampling site during high wind speed (< 7 m s⁻¹) were also displayed in this study. In addition, the correlation coefficients between TSP, PM_2.5 and PM_2.5−10 of ionic species vs. high wind speed were also observed. The results indicated that the correlation coefficient order was TSP > PM_2.5−10 > PM_2.5 for particle at both sampling sites near Taiwan strait. In addition, the concentration of Cl⁻, NO₃ ⁻, SO₄ ²⁻, NH₄ ⁺, Mg²⁺, Ca²⁺ and Na⁺ were also analyzed in this study.     

Diatoms as indicators in the Environmental Monitoring and Assessment Program-Surface Waters (EMAP-SW)

As a part of the U.S. Environmental Protection Agency's Environmental Monitoring and Assessment Program-Surface Waters (EMAP-SW), sedimentary diatom assemblages were studied from 66 lakes in the northeastern U.S.A. to evaluate the applicability of diatoms for this nation-wide monitoring program. Sediment cores were collected from the study lakes and diatoms were analyzed from the top (present-day) and bottom (pre-industrial) sediment samples. Canonical correspondence analysis (CCA) was used to examine which environmental variables correlate most closely with the distributions of diatom taxa in the top (surface) samples. Forward selection and Monte Carlo permutation tests showed that diatom species distributions were significantly related to total lakewater phosphorus (TP), pH, chloride, Secchi depth, and lake size and maximum depth. We developed weighted-averaging calibration and regression models for inferring TP (r ²=0.62), chloride (r ²=0.61), pH (r ²=0.86), and Secchi depth (r ²=0.62). An index of overall lake disturbance was also developed. Our diatom data indicate that marked changes have occurred in the study lakes since pre-industrial times as a result of anthropogenic activity.     

Substrate influence on epiphytic lichens

The origin of the presence of soil elements in the epiphytic lichen Lecanora conizaeoides was investigated in an area of heavily polluted soil (The Broekpolder The Netherlands). Analysis results of lichens, bark and tree rings of the supporting trees indicated that for As, Co, Cr, Cu, Fe, Hg, Sc and V the levels in lichens may be considered to originate from wet and dry deposition. The Cd, Mn and Zn levels in lichens might have originated from both wet and dry deposition and the substrate bark. For these three elements, in particular, accumulation characteristics in lichens should be further investigated.     

Heavy metals regulate physiological and behavioral events by modulating ion channels in neuronal membranes of molluscs

The interaction of heavy metals (HgCl₂, CdCl₂, CuCl₂, PbCl₂ and ZnCl₂) and neurotransmitters (ACh, 5HT and DA) was studied on the excitable membrane of identified neurons of Lymnaea stagnalis and Helix pomatia. It was shown that,

1. The excitability and chemosensitivity of molluscan neurons were modified under the influence of the heavy metals Hg²⁺, Cd²⁺, Cu²⁺, Pb²⁺ and Zn²⁺.
2. Change in excitability to transmitters occurred as a potentiation or depression of the evoked response both in duration of membrane polarization and in frequency of spike activity.
3. The chemosensitivity changes in various ways, namely:
4. excitatory effect was totally eliminated;
5. one component of the effect was depressed.
Different neurons may show different reactions to the same heavy metal.
6. There were differences in the effects of various heavy metals. Hg²⁺ has a more generalized effect than Cd²⁺; Cu²⁺, Pb²⁺ and Zn²⁺ were less effective in a number of neurons. The heavy metal effect was dose dependent, too.
7. Both inward and outward currents, which were evoked by neurotransmitters or voltage induced, were modified in most of the tested neurons. Both an increase and decrease of the membrane permeability occurred in different neurons in response to the same or different heavy metals.
8. The changes can be interpreted as a result of
9. direct effect on specific ionic channels;
10. modification of receptors binding ACh, 5HT, or DA;
11. modification of intracellular processes responsible for the regulation of membrane permeability.

     

Assessment of geospatial and hydrochemical interactions of groundwater quality,southwestern Nigeria

Groundwater pollution resulting from anthropogenic activities and poor effluent management is on the rise in Nigeria. Hence, groundwater used for domestic purposes is questionable and therefore calls for scientific scrutiny. Investigation of hydrochemical interactions and quality of groundwater resource is essential in order to monitor and identify sources of water pollutants. As a result, groundwater samples were collected from 21 locations in Abeokuta South, Nigeria and analyzed for physicochemical parameters using standard methods. Results obtained were subjected to hydrochemical and geospatial analyses. Water quality parameters investigated exhibited wide variations from location to location. Fe²⁺, Mg²⁺, SO₄^2?, Cl^?, total hardness (TH), Mn, Na⁺, NO₃^?, SiO₂, and alkalinity exhibited the highest levels of variation with coefficients of variation of 131.3, 92.8, 83.9, 76.7, 65.9, 64.3, 57.6, 57.2, 57.0, and 52.5, respectively. The average pH value was 6.76 with 71% of the water samples being slightly acidic. Na²⁺, Mg²⁺, Fe²⁺, and EC contents exhibited the most violation of drinking water standards with percent violations of 100, 52.4, 47.6, and 47.6%, respectively. Parameters, such as Mn, Ca²⁺, NO₃^?, and CO₃^2?, were within the WHO guideline values for drinking water in all the samples. The highest level of significant correlation was found to exist between Na⁺ and Cl^? (r?=?0.84, α?=?0.01). Six principal components, which explained 83.5% of the variation in water quality, were extracted with the first (34.1%) and second components (15.7%) representing the influence of mineral dissolution and anthropogenic practices, respectively, on the hydrochemistry of the area. Four hydrochemical clusters were identified with distinctly partitioned water quality. Further analysis revealed that 38, 29, 24, and 9% of the samples were the Na-K-HCO₃, Na-K-Cl-SO₄, Ca-Mg-HCO₃, and Ca-Mg-Cl-SO₄ types, respectively. Anthropogenic activities are increasing threat to groundwater quality in the study location and therefore call for urgent attention. There is also a need for routine monitoring of groundwater in Abeokuta.     

Prediction of the solubility of zinc, copper, nickel, cadmium, and lead in metal-contaminated soils

Risk assessment of metal-contaminated soil depends on how precisely one can predict the solubility of metals in soils. Responses of plants and soil organisms to metal toxicity are explained by the variation in free metal ion activity in soil pore water. This study was undertaken to predict the free ion activity of Zn, Cu, Ni, Cd, and Pb in metal-contaminated soil as a function of pH, soil organic carbon, and extractable metal content. For this purpose, 21 surface soil samples (0–15 cm) were collected from agricultural lands of various locations receiving sewage sludge and industrial effluents for a long period. One soil sample was also collected from agricultural land which has been under intensive cropping and receiving irrigation through tube well water. Soil samples were varied widely in respect of physicochemical properties including metal content. Total Zn, Cu, Ni, Cd, and Pb in experimental soils were 2,015?±?3,373, 236?±?286, 103?±?192, 29.8?±?6.04, and 141?±?270 mg kg^?1, respectively. Free metal ion activity, viz., pZn²⁺, pCu²⁺, pNi²⁺, pCd²⁺, and pPb²⁺, as estimated by the Baker soil test was 9.37?±?1.89, 13.1?±?1.96, 12.8?±?1.89, 11.9?±?2.00, and 11.6?±?1.52, respectively. Free metal ion activity was predicted by pH-dependent Freundlich equation (solubility model) as a function of pH, organic carbon, and extractable metal. Results indicate that solubility model as a function of pH, Walkley–Black carbon (WBC), and ethylenediaminetetraacetic acid (EDTA)-extractable metals could explain the variation in pZn²⁺, pCu²⁺, pNi²⁺, pCd²⁺, and pPb²⁺ to the extent of 59, 56, 46, 52, and 51 %, respectively. Predictability of the solubility model based on pH, KMnO₄-oxidizable carbon, and diethylenetriaminepentaacetic acid-extractable or CaCl₂-extractable metal was inferior compared to that based on EDTA-extractable metals and WBC.