Integrated Flow-based System Displaying an In-line Mini Soil Column to Monitor Iron Species in Soils Leachates

ABSTRACT

Contamination of ground water as a consequence of soil leaching processes is an issue of major concern. In this context, a simulation of the soil leaching process was designed. A sequential injection (SI) method to monitor the soil leaching of iron complexes with in-line rain simulation for leachate production is described. The developed methodology comprises the SI determination of both iron(III) and 3-hydroxy-4-pyridinones iron(III) complexes, coupled to a mini soil column (mSC) for displaying in-line rain simulations. The described SI method enabled iron(III) determination within the range 2.0–35 µmol L^?1, with a detection limit of 0.42 µmol L^?1, and determination of iron(III) complexes in the range 1.0–45 µmol L^?1. It was successfully applied to leachates from laboratory scale soil columns (LSSC), with good precision for both iron(III) and iron complexes determinations: calculated relative standard deviation (RSD) of 5% and 6%, respectively. A step further in automation and miniaturization was attained with the incorporation of a mini soil column for the in-line leachate production. The system enabled the soil leachate production and assessment in less than 5 min, including determinations in triplicate.     

Optimizing the Nutritional Status of a Typic Kandiustult of Kerala,India, Using Sorption Study

Abstract

Nutrient sorption studies were carried out as a part of a mega project on “Yield maximization in cassava (Manihot esculenta Crantz) through systematic approach in fertilizer use” to find out the sorption characteristics of major, secondary, and micronutrients [i.e., phosphorus (P), potassium (K), sulfur (S), copper (Cu), zinc (Zn), manganese (Mn), and boron (B)] in a typic kandiustult of Kerala, India. The sorption curve fitted by using this study along with the results of preliminary soil analysis and critical level of these nutrients were used to optimize the nutritional status of this soil. Sorption study revealed that P, K, S, and B were limiting and others were sufficient for this soil. The quantities of the limiting nutrients required to optimize the soil nutritional status were estimated from the sorption curve as P, K, S, and B at 136 µg mL^?1, 0.338 meq 100 mL^?1, 20 µg mL^?1, and 6.025 µg mL^?1, respectively.     

Magnetic Solid-Phase Extraction Based on Modified Iron Oxide Nanoparticles for the Preconcentration of Ultra-Trace Amounts of Copper Ions in the Environmental and Plant Samples and its Determination Using FAAS

In the present work, magnetic iron oxide nanoparticles (MIONPs) coated with sodium dodecyl sulfate (SDS) and modified with 1-(2-pyridylazo)-2-naphthol (PAN) as a new nanoparticle were prepared and used as an adsorbent for the extraction and preconcentration of copper ions. After adsorption, copper ions were desorbed with nitric acid (HNO₃), followed by determination with flame atomic absorption spectrometry (FAAS). The extraction conditions0. were investigated systematically. The linear range 3.0–500.0 ng mL^?1 and the detection limit of 0.6 ng mL^?1 were obtained. The relative standard deviation (RSD) of the method for seven replicate determinations of 0.1 µg mL^?1 of Cu(II) was 2.2%. The method was applied for the determination of Cu(II) in different water samples with good trueness. The accuracy was also evaluated through analyses of a certified reference material (CRM TMDW-500).     

Separation of Ag(I) Ions from Lepidium draba L. Plant and Water and Standard Samples by Carrier Element-Free Coprecipitation Method Prior to their Flame Atomic Absorption Spectrometric Determination

In this work, silver iodide (Ag(I)) ions were separated via the carrier element-free coprecipitation (CEFC) method using an organic coprecipitating agent, 1,6-diamino-4-(4-chlornphenyl)-2-oxo-1,2-dihydropyridine-3,5-dicarbonitrile [DCODD] prior to its determination by ?ame atomic absorption spectrometry (FAAS). Analytical parameters including pH of aqueous solution, amount of DCODD, standing time, centrifugation rate and time, and sample volume were studied and optimized. Under the best experimental conditions, it was found that extraction can be performed from the sample volume of 500.0 for silver ion (preconcentration factor of 100.0). Linearity was maintained between 0.006 and 1.50 µg.mL^?1 for silver. Detection limit for silver based on 3Sb was 1.60 ng.mL^?1. The relative standard deviation of eight replicate measurements of 0.20 µg.mL^?1of silver was 2.10%. Finally, the developed method was successfully applied to extraction and determination of the silver ions in the Lepidium draba L plant, water and standard samples and satisfactory results were obtained.     

Yield Maximization in Cassava through a Systematic Approach in Fertilizer Use

Abstract

Maximum yield research (MYR) and maximum economic yield systems (MEY) are important under the present situation of increased demographic changes, which have reduced the per capita availability of both land and food. Among root and tuber crops, cassava is found in a variety of production systems and performs well under various levels of management from low‐input to high‐input systems. A systematic approach in fertilizer use involves the determination and elimination of soil nutrient constraints for balanced supply of all potentially deficient essential nutrients for sustainable high yield. In the systematic approach of determining optimal fertilizer for cassava (Manihot esculenta Crantz) in a Typic Kandiustult soil of Kerala, India, studies on critical levels of nutrients, original nutritional status of the soil, its sorption capacity, and greenhouse/screenhouse nutrient survey were carried out. The critical levels of phosphorus (P) and potassium (K) were determined as 8.23 and 43.5 µg g^?1, respectively. The preliminary analysis of the soil of the experimental site revealed the overall fertility status as very poor. The sorption studies conducted for P, K, copper (Cu), zinc (Zn), manganese (Mn), sulfur (S), and boron (B) indicated P, K, S, and B were limiting in this particular soil. The quantities of these nutrients needed to optimize the soil nutrient status were determined from the preliminary soil analysis, critical levels of nutrients, and sorption curves and found to be 136 µg mL^?1 P, 0.338 meq 100 mL^?1 K, 20 µg mL^?1 S, and 6.025 µg mL^?1 B, respectively. From the greenhouse nutrient survey, N, P, K, and calcium (Ca) were seen as limiting nutrients for this soil; therefore the optimum treatment for cassava was fixed as N‐P‐K at 100:300:300 kg ha^?1, respectively. Field experiments were conducted for two seasons with different levels of the optimum treatment using a short duration (6–7 months) cassava variety, Sree Vijaya. The optimum treatment gave a yield of 43.41 t ha^?1, whereas the yield under the existing practice recommendations was 20–25 t ha^?1. Economic analysis showed this optimum treatment as the best in terms of highest gross return (Rs 1,31,125/‐), net return (Rs 83,150/‐), added return (Rs 70, 178/‐), added profit (Rs 56,142/‐), and benefit cost ratio (BCR) (2.73).     

Chromium Speciation in Water by Sorption on Calcite and Determination by Electrothermal Atomic Absorption Spectrometry

Abstract

A rapid, sensitive, and accurate method for the separation and speciative determination of chromium (Cr)(VI) and Cr(III) in water samples has been developed using sorption as the separation technique in conjunction with final determination by electrothermal atomic absorption spectroscopy (ETAAS). The present method, where granular calcite is used as selective sorbent, separates Cr(III) with retention values up to 99%, resulting in high accuracy determination of Cr(VI). Total Cr was likewise determined by ETAAS after an efficient reduction of Cr(VI) to Cr(III) using ascorbic acid as reducing agent, deriving Cr(III) concentration from the difference between total Cr and Cr(VI). The parameters of the separation technique, solution pH (4.5–5.5), solution flow rate through the calcite column (0.14–0.42 mL min^?1), and calcite column internal diameter (1.5–3.0 cm), were evaluated. Best results were achieved with pH of 5.5, flow rate of 0.42 mL min^?1, and column internal diameter of 1.5 cm. Optimum determination conditions were found using magnesium nitrate [Mg(NO₃)₂] as chemical modifier, pyrolysis, and atomization temperatures of 1400 and 2200°C, respectively. In such conditions, the detection limits (n=10) were 1.5 and 0.8 µg L^?1 for Cr(III) and Cr(VI), respectively.     

Graphite Furnace Atomic Absorption Spectrometry After Dispersive Liquid–Liquid Microextraction for the Determination of Selenium in the Anodic Slime

In the present study, a method based on dispersive liquid–liquid microextraction (DLLME) followed by graphite furnace atomic absorption spectrometry (GFAAS) determination was proposed for the determination of selenium by using ammonium pyrrolidine dithiocarbamate (APDC) as the chelating reagent. The main factors influencing the DLLME were investigated systematically. Under the optimal conditions, the limit of detection for Se(IV) was 0.02 ng mL^?1. The relative standard deviation was 4.1% (C_Se(IV) = 0.2 ng mL^?1, n = 8) with an enhancement factor of 135.8-fold from only 5 mL of the water sample. The proposed method was successfully applied to the determination of Se(IV) in anodic slime and electrolyte samples. In order to validate the proposed method, a Certified Reference Material (trace elements in water, 1643e, NIST) was analyzed, and the determined value obtained was in good agreement with the certified value.     

Determination of Trace Amounts of Cadmium Ions in Water and Plant Samples Using Ligand-Less Solid Phase Extraction-Based Modified Co3O4 Nanoparticles

In this study, a new Co₃O₄ nanoparticles (NPs) coated with sodium dodecyl sulphate (SDS) is developed for preconcentration of trace amounts of cadmium ions (Cd ²⁺) as a prior step to its determination by flame atomic absorption spectrometry (FAAS). The effects of various parameters, including pH of sample solution, amount of sorbent, flow rates of solution and eluent, sample volume, type, and least amount of the eluent for elution of the Cd ²⁺ from Co₃O₄ NPs were studied and optimized. Experimental conditions for effective separation of trace levels of the Cd ²⁺were optimized with respect to different experimental parameters in Column method. Under the best experimental conditions, the calibration curve was linear in the range of 1.0–500.0 ng.mL^?1 of cadmium (Cd) with R² = 0.999. The detection limit was 0.4ng.mL^?1 in the original solution (3S_b/m) and the relative standard deviation for eight replicate determination of 0.1µg.mL^?1 Cd was ±2.1%. The method was validated by the analysis of a certified reference material with the results being in agreement with those quoted by manufactures. The developed method was successfully applied to the extraction and determination of Cd in water and food samples with satisfactory results.     

Seasonal variations in the abundance of virus-like particles and bacteria in the floodwater of a Japanese paddy field

Abstract

Viruses are the most abundant biological entities in marine and freshwater environments. Many studies have shown the ecological importance of viruses in the primary production and microbial food web in aquatic environments. However, no studies have examined viral abundance in the floodwater of paddy fields. The present study surveyed the abundance of virus-like particles (VLPs) and bacteria in the floodwater of a Japanese paddy field under a long-term fertilizer trial since 1925 during the rice cultivation period. Virus-like particles and bacterial abundances in the floodwater ranged from 5.6 × 10⁶ to 1.2 × 10⁹ VLPs mL^?1 and from 9.2 × 10⁵ to 4.3 × 10⁸ cells mL^?1 with mean abundances of 1.5 × 10⁸ VLPs mL^?1 and 5.1 × 10⁷ cells mL^?1, respectively, and increased with an increase in the turbidity of the floodwater with suspended particles. The magnitude of seasonal variation was more than 50-fold for VLP abundance and 100-fold for bacterial abundance. The virus-to-bacterium ratios fluctuated over the rice cultivation period, ranging from 0.11 to 72 and their increase correlated with the decrease in bacterial abundance. Our results suggest that viral abundance in the floodwater of paddy fields is larger than in natural marine and freshwater environments.     

Spectrophotometric Determination of Nickel(II) in Soil and Standard Alloy Samples Using 5-Methyl-2-acetylfuran-4-methyl-3-thiosemicarbazone (5-MAFMT)

A simple and selective spectrophotometric method was developed for the determination of nickel(II) using 5-methyl-2-acetylfuran-4-methyl-3-thiosemicarbazone (5-MAFMT) as a chromogenic reagent forming a yellow-colored complex at pH 9.5. The complex was instantaneous and stable for 5 h. The system obeyed Beer’s law in the concentration range of 0.06–0.60 µg/mL of nickel(II), with a correlation coefficient of 0.999. The molar absorptivity and Sandell’s sensitivity of the complex species were found to be 1.87 × 10⁴ L/mol.cm and 1.2 × 10^–3 µg/cm² at 361 nm, respectively. The limit of detection was 0.0713 µg/mL with the relative standard deviation (RSD) ≤1.0%. The proposed method is rapid, simple, sensitive, and successfully applied for the determination of nickel(II) when present alone or in the presence of other ions that are usually associated with nickel(II). The method was tested for nickel (II) determination in soil and various standard alloy samples. The recovery of nickel(II) in alloy samples using the developed method was >98% confirming the suitability of the method. Comparisons of the results with those obtained using an atomic absorption spectrophotometer for nickel(II) determination also tested the validity of the method at the 0.05 level.     

Diversity of endophytic actinomycetes in mandarin grown in northern Thailand,their phytohormone production potential and plant growth promoting activity

Abstract

The rapid expansion of mandarin (Citrus reticulata L.) production areas with high agrochemical input in the highland areas of northern Thailand has resulted in negative effects in terms of production, environment, soil quality, and public health. The use of microorganisms as plant growth promoters is an alternative method to reduce agrochemical input. Thus, we studied the diversity of endophytic actinomycetes in mandarin and their potential as plant growth promoters. A total of 252 endophytic actinomycete isolates were recovered from mandarin. Based on spore chain morphology, cell wall type, and 16S rRNA gene sequence, the isolates were classified into six genera: Streptomyces, Nocardia, Nocardiopsis, Spirillospora, Microbispora and Micromonospora. The most frequent isolates recovered were members of Streptomyces (85.3%). Selected isolates (64 isolates) from these genera were evaluated for their indole-3-acetic acid (IAA) production potential in a medium with 2 mg mL^?1 tryptophan, and all the selected isolates showed the potential to produce IAA, with average values of IAA production of 13.34, 3.36, 140.38, 12.55, 1.40, and 6.19 µg IAA mL^?1, respectively. Isolates of genus Nocardiopsis showed a very high ability to produce IAA that was the highest among all the genera, with values ranging from 62.23 to 222.75 µg mL^?1. Twelve isolates selected from these genera were inoculated onto mandarin seedlings, and the results indicated that the shoot height, fresh shoot weight and fresh root weight of the seedlings were promoted by the inoculation of endophytic actinomycetes, with values ranging from 20.2 to 49.1%, 14.9 to 53.6%, and 1.6 to 102% over the control, respectively.     

Automated Modification of the Molybdenum Blue Colorimetric Method for Phosphorus Determination in Soil Extracts

A flow injection analysis (FIA) method capable of automation for molybdate reactive phosphorus (P) determination in soil extracts is described. Results obtained using this method in three soil extracts [calcium chloride (CaCl₂), Olsen, and Mehlich I] were the same as those provided by the manual molybdate blue colorimetric method. Linear range extending to 2 mg P L^?1, detection limits ranging from 6 to 26 µg L^?1 depending on the soil extract, and accurate recoveries from P‐spiked samples were achieved. The sensitivity of the system was around 0.3 absorbance units per mg P L^?1, and the sampling frequency was 72 samples h^?1, higher than those described for most of the flow injection methods.     

A Sensitive Spectrophotometric Method for Determination of Trace Quantities of Indium in Soil

A simple and very sensitive method determining microgram quantities of indium in soil has been developed. The spectrophotometric method (??=?1.74?×?10⁵ l mol^-1 cm^-1) based on the mixed complex In (III) with Chrome Azurol S and benzyldodecyldimethylammonium bromide was used for the analysis. A preliminary separation is made by extracting indium into butyl acetate from 5 M HBr solution. The selectivity of indium extraction and determination in the presence of macro- and micro components of soil was studied. Prior reduction of Fe (III) to Fe (II) with ascorbic acid prevents its co-extraction with indium. Indium was determined in synthetic mixtures corresponding to soil compositions and real samples of soil from different agricultural and industrial regions of Poland. The content of indium was found from the calibration graph (in the range, 0.12–0.48 μg/ml; r?=?0.9991) obtained after extraction. The precision was satisfactory: % RSD (n?=?6) ranged from 2.7 to 8.2. The average indium standard recovery ranged from 95 to 101%. Analysis using an ICP-OES method gave comparable results.     

A Study on Al(III) and Fe(II) Ions Sorption by Cattle Manure Vermicompost

Cattle manure vermicompost has been used for the adsorption of Al(III) and Fe(II) from both synthetic solution and kaolin industry wastewater. The optimum conditions for Al(III) and Fe(II) adsorption at pH?2 (natural pH of the wastewater) were particle size of ≤250?µm, 1 g/10 mL adsorbent dose, contact time of 4 h, and temperature of 25°C. Langmuir and Freundlich adsorption isotherms fitted reasonably well in the experimental data, and their constants were evaluated, with R ² values from 0.90 to 0.98. In synthetic solution, the maximum adsorption capacity of the vermicompost for Al(III) was 8.35 mg g^?1 and for Fe(II) was 16.98 mg g^?1 at 25°C when the vermicompost dose was 1 g 10 mL^?1, and the initial adjusted pH was 2. The batch adsorption studies of Al(III) and Fe(II) on vermicompost using kaolin wastewater have shown that the maximum adsorption capacities were 1.10 and 4.30 mg g^?1, respectively, at pH?2. The thermodynamic parameter, the Gibbs free energy, was calculated for each system, and the negative values obtained confirm that the adsorption processes were spontaneous.     

Microfauna Community as an Indicator of Effluent Quality and Operational Parameters in an Activated Sludge System for Treating Piggery Wastewater

In order to study the potential use of microfauna as an indicator of effluent quality and operational parameters in an activated sludge system for treating piggery wastewater, an experimental sequencing batch reactor was set up and evaluated by biological and physical–chemical analyses for 12 months. Results show that microfauna (and specifically ciliate protozoa) are a good parameter for assessing effluent quality in terms of both chemical oxygen demand (COD) and ammonia and for assessing the organic and nitrogen load of the system. Specifically, the abundance of ciliates decreases from 20,000 individuals·mL^?1 to ca. 2,500 individuals·mL^?1 and from ca. 10,000 individuals mL^?1 to ca. 200 individuals mL^?1 when effluent concentration is between 550 and 750 mg L^?1 and above 100 mg L^?1 to the COD and ammonia concentrations, respectively. Furthermore, microfauna abundance is reduced from ca. 18,000 individuals mL^?1 (organic load between 0.1 and 0.2 mg COD mg total suspended solids (TSS)^?1 day^?1) to ca. 500 individuals mL^?1 (organic load between 0.3 and 04 mg COD mg TSS^?1 day^?1). Microfauna abundance also decreases as nitrogen loading increases. Nitrogen loading in the range of 5–60 mg NH₄–N g TSS^?1 day^?1 does not have any significant effect on microfauna abundance. However, ammonia loading from 60 to 120 mg NH₄–N g TSS^?1 day^?1 reduces microfauna abundance ca. 6-fold. Ciliate protozoa were the largest microfauna group during the whole period of study, representing ca. 75% of the total microfauna abundance. The largest group in the ciliate community was that of the free-swimming ciliates. This was followed by the group of attached and crawling ciliates. Specifically, the dominant ciliate species during the whole study period were Uronema nigricans, Vorticella microstoma-complex, Epistylis coronata, and Acineria uncinata.     

Substrate‐Induced Respiration of a Sandy Soil Treated with Different Types of Organic Waste

A sandy soil was amended with different types of sewage sludge (digested, dried, and composted) and pig slurry. The composted sludges displayed higher organic‐matter stability (39–45%) than only digested sludge (26–39%) or digested + dried sludge (23–32%). The microbial biomass of the dried sludge was undetectable. Digested and composted sludges and pig slurry displayed microbial biomasses (12492–13887 µg g^?1, 1221–2050 µg g^?1, and 5511 µg g^?1, respectively) greater than the soil (108 µg g^?1). The wastes were applied at seven doses, ranging from 10 to 900 g kg^?1. Soils were incubated for 28 days. Substrate‐induced respiration (SIR) was measured for 12 consecutive hours on day 1 and on day 28. The results showed that SIR increased with the dose of organic amendment. However, SIR decreased when moderate doses of pig slurry or high doses of digested + dried sludge were tested. The possibility of using this inhibition as an ecotoxicological indicator is discussed.     

Concentrations and Exports of Fecal Indicator Bacteria in Watersheds with Varying Densities of Onsite Wastewater Systems

The research goal was to determine if onsite wastewater system (OWS) density had an influence on the concentrations and watershed exports of Escherichia coli and enterococci in urbanizing watersheds. Eight watersheds with OWS densities ranging from <?0.1 to 1.88 systems ha^?1 plus a watershed served by sewer (Sewer) and a mostly forested, natural watershed (Natural) in the Piedmont of North Carolina served as the study locations. Stream samples were collected approximately monthly during baseflow conditions between January 2015 and December 2016 (n?=?21). Median concentrations of E. coli (2014 most probable number (MPN) 100 mL^?1) and enterococci (168 MPN 100 mL^?1) were elevated in streams draining watersheds with a high density of OWS (>?0.77 system ha^?1) relative to watersheds with a low (<?0.77 system ha^?1) density (E. coli: 204 MPN 100 mL^?1 and enterococci: 88 MPN 100 mL^?1) and control watersheds (Natural: E. coli: 355 MPN 100 mL^?1 and enterococci: 62 MPN 100 mL^?1; Sewer: 177 MPN 100 mL^?1 and 130 MPN 100 mL^?1). Samples collected from watersheds with a high density of OWS had E. coli and enterococci concentrations that exceeded recommended thresholds 88 and 57% of times sampled, respectively. Results show that stream E. coli and enterococci concentrations and exports are influenced by the density of OWS in urbanizing watersheds. Cost share programs to help finance OWS repairs and maintenance are suggested to help improve water quality in watersheds with OWS.     

Occurrence and Geochemistry of Arsenic in Groundwater of Punjab,Northwest India

Abstract

Arsenic (As) is a deadly poison at high concentrations. It is mysterious in the sense that people are exposed to it most of the time through drinking groundwater, fortunately at much lower concentrations than the deadly levels, and usually without knowing it. Arsenic content in alluvial aquifers of Punjab varied from 3.5 to 688 µg L^?1. Arsenic status of groundwater is classified into low (<10 µg L^?1), moderate (≥10 to <25 µg L^?1), high (≥25 to <50 µg L^?1), and very high (>50 µg L^?1). In zone I, the concentration of As in groundwater varied from 3.5 to 42 µg L^?1 with a mean value of 23.4 µg L^?1. On the basis of these limits, only 8% of samples were low, whereas 51 and 41% of the total samples collected from this region fall in the moderate and high As categories. The concentration of As in groundwater of zone II varied from 9.8 to 42.5 µg L^?1 with a mean value of 24.1 µg L^?1. Arsenic concentration in the alluvial aquifers of the central plain of zone II is 2 and 52% in the low and moderate limits. In this region, 46% of groundwater sites contain high As concentrations. Arsenic concentrations in the aridic southwestern parts are significantly different from other two provinces. The As concentration ranged from 11.4 to 688 µg L^?1 with average value of 76.8 µg L^?1. Eleven percent of the aquifers of the southwestern region of zone III are in the moderate category, 54% in the high, and 35% in the very high. According to safe As limits (<10 µg L^?1), only 3 and 1% of the groundwater samples collected from zones I and II were fit for dinking purposes with respect to As content. In the aridic southwest, zone III, all water samples contained As concentrations greater than the safe limits and thus are not suitable for drinking purposes. The presence of elevated As concentrations in groundwater are generally due to the results of natural occurrences of As in the aquifer materials. The concentration of other competitive oxyanions in waters such as phosphate, sulfate, and borate also depressed the adsorption of As on the sorption sites of aquifer materials and thereby eventually elevate the As concentration in groundwaters. In groundwater of alluvial aquifers of Punjab, released from sulfide oxidation and oxyhydroxide of iron, elevated (>10 µg L^?1) concentrations of As were widespread because of high pH (>8.0) and higher concentrations of phosphate, borate, sulfate, and hydroxyl anions. It is conclusively evident that geochemical conditions, such as pH, oxidation–reduction, associated or competing ions, and evaporative environments have significant effects on As concentration in groundwater. These conditions influence how much As is dissolved or precipitated into the water and how much is bound to the aquifer materials or the solid particles in water.     

Zinc Tolerance in Wheat Cultivars as Affected by Varying Levels of Phosphorus

Abstract

The effect of zinc–phosphorus (Zn‐P) interaction on Zn efficiency of six wheat cultivars was studied. The higher dry matter yields were observed when Zn was applied at 5 µg g^?1 soil than with no Zn application. Phosphorus applications also increased dry matter yield up to the application of 25 µg P g^?1 soil. The dry matter yield was significantly lower at the P rate of 250 µg g^?1 soil. At the Zn‐deficient level, the Zn‐efficient cultivars had higher Zn concentrations in the shoots. Zinc concentrations in all cultivars increased when the P level in the soil was increased from 0 to 25 µg P g^?1 soil except for the cv. Durati, in which Zn concentrations decreased with increases in P levels. However, when Zn×P interactions were investigated, it was observed that at a Zn‐deficient level, Zn concentrations in the plant shoot decreased with each higher level of P, and more severe Zn deficiency was observed at P level of 250 µg g^?1 soil.     

Spectrophotometric and Inductively Coupled Plasma–Optical Emission Spectroscopy Determination of Gallium in Natural Soils and Soils Polluted by Industry: Relationships between Elements

The aim of this work was to determine gallium contents in different soils of Poland using a sensitive spectrophotometric method based on the complex of Ga(III) with chrome azurol S and benzyldodecyldimethylammonium bromide and inductively coupled plasma–optical emission spectrometry technique. The total content of gallium in the soils clearly depends on the soil location and properties and ranged from 41.7 to 437 μg g^–1. The contents of gallium determined in 10% nitric acid and 1 M of magnesium chloride extract ranges respectively from 38.0 to 81.9% and 20–40% of the total content of this element. A strong correlation has been found between gallium and zinc, cadmium, lead, and copper. The high Pearson correlation coefficient values and the proportional relationship between the concentrations of Ga and these metals may make it possible to treat gallium as an indicator of soil contamination with heavy metals.