Integrated Approach to Hydrogeochemical Assessment of Groundwater Quality in Major Industrial Zone of Punjab, Pakistan.

Groundwater contamination with arsenic (As) is a significant concern in Pakistan's Punjab Province. This study analyzed 69 groundwater samples from Faisalabad, Gujranwala, Lahore, and Multan to understand hydrogeochemistry, health impacts, contamination sources, and drinking suitability. Results revealed varying as concentrations across districts, with distinctive cation and anion orders. Faisalabad exhibited Na+ > Mg2+ > Ca2+ > K+ > Fe2+ for cations and SO42- > Cl- > HCO3- > NO3- > F- for anions. Gujranwala showed Na+ > Ca2+ > Mg2+ > K+ for cations and HCO3- > SO42- > Cl- > NO3- > F- for anions. In Lahore, demonstrated: Na+ > Ca2+ > Mg2+ > Fe > K+ for cations and HCO3- > SO42- > Cl- > NO3- > F- for anions. Multan indicated K+ > Ca2+ > Mg2+ > Na+ > Fe for cations and HCO3- > SO42- > Cl- > F- > NO3- ) for anions. Hydrochemical facies were identified as CaHCO3 and CaMgCl types. Principal Component Analysis (PCA), highlighted the influence of natural processes and human activities on groundwater pollution. Water Quality Index (WQI) result reveal that most samples met water quality standards. The carcinogenic risk values for children exceeded permissible limits in all districts, emphasizing a significant cancer risk. The study highlights the need for rigorous monitoring to mitigate (As) contamination and protect public health from associated hazards.

Understanding the role of the fructose-1,6-bisphosphatase gene for enhancing the photosynthetic rate in Arabidopsis thaliana.

Transgenic Arabidopsis thaliana (ecotype Columbia) was successfully transformed with the gene fructose-1,6-bisphosphatase (FBPas e) and named as AtFBPase plants. Transgenic plants exhibited stable transformation, integration and significantly higher expressions for the transformed gene. Morphological evaluation of transgenic plants showed increased plant height (35cm), number of leaves (25), chlorophyll contents (28%), water use efficiency (increased from 1.5 to 2.6µmol CO2 µmol-1 H2 O) and stomatal conductance (20%), which all resulted in an enhanced photosynthetic rate (2.7µmolm-2 s-1 ) compared to wild type plants. This study suggests the vital role of FBPase gene in the modification of regulatory pathways to enhance the photosynthetic rate, which can also be utilised for economic crops in future.

First identification of potato tuber rot caused by Penicillium solitum, its silver nanoparticles synthesis, characterization and use against harmful pathogens.

Potato is one of the highly consumed vegetable crop grown in different regions across Pakistan that is affected by fungal diseases. The current research was conducted to identify fungal pathogen causing mold-like disease of potato in Khyber Pakhtunkhwa (KP), Pakistan. For molecular identification and characterization of the fungal disease; potato tuber samples were collected followed by culturing on potato dextrose agar (PDA). Based on morphological features, the pathogen was identified as a Penicillium species. This result was obtained in 45 different isolates from potato tubers. Molecular identification was done using ß-tubulin primers and ITS5 sequencing of 13 different isolates that releveled 98% homology with BLAST (GenBank accession no. KX958076) as Penicillium solitum (GenBank accession nos. ON307317; ON307475 and ON310801). Phylogenetic tree was constructed that showed Penicillium solitum prevalence along with Penicillium polonicum and Penicillium citrinum on potato tubers. Based on this, Penicillium solitum based silver nanoparticles (Ag NPs) were synthesized and characterized using UV-visible spectroscopy, Fourier transform infrared (FTIR) spectroscopy, X-ray diffraction (XRD), energy dispersive X-ray (EDX) and field emission scanning electron microscopy (FE SEM). UV-analysis showed a characteristic peak at 410 nm confirming synthesis of Penicillium solitum based Ag NPs. This was further confirmed by XRD followed by EDX and SEM that showed face cubic crystal structure with Ag as major constituent of 18 nm formed spherical Ag NPs. FTIR showed band stretching of O-H, N-O and C-H of biological origin. Similarly, Penicillium solitum based Ag NPs presented strong anti-bacterial and anti-fungal activity at 0.5 level of significance LSD. According to our knowledge, this is the first report of Penicillium solitum identification in Pakistan, its Ag NPs synthesis and characterization to be used against pathogens of agricultural significance.

Genome-Wide Characterization and Sequence Polymorphism Analyses of Glycine max Fibrillin (FBN) Revealed Its Role in Response to Drought Condition.

The fibrillin (FBN) gene family is widely distributed in all photosynthetic organisms. Members of this gene family are involved in plant growth and development and their response to various biotic and abiotic stress factors. In this study, 16 members of FBN were identified in Glycine max and characterized by using different bioinformatics tools. Phylogenetic analysis classified FBN genes into seven groups. The presence of stress-related cis-elements in the upstream region of GmFBN highlighted their role in tolerance against abiotic stresses. To further decipher the function, physiochemical properties, conserved motifs, chromosomal localization, subcellular localization, and cis-acting regulatory elements were also analyzed. Gene expression analysis based on FPKM values revealed that GmFBNs greatly enhanced soybean drought tolerance and controlled the expression of several genes involved in drought response, except for GmFBN-4, GmFBN-5, GmFBN-6, GmFBN-7 and GmFBN-9. For high throughput genotyping, an SNP-based CAPS marker was also developed for the GmFBN-15 gene. The CAPS marker differentiated soybean genotypes based on the presence of either the GmFBN-15-G or GmFBN-15-A alleles in the CDS region. Association analysis showed that G. max accessions containing the GmFBN-15-A allele at the respective locus showed higher thousand seed weight compared to accessions containing the GmFBN-15-G allele. This research has provided the basic information to further decipher the function of FBN in soybean.

Antioxidant, Cytotoxic, and Antimicrobial Potential of Silver Nanoparticles Synthesized using Tradescantia pallida Extract.

Silver nanoparticles have received much attention, due to their wide range of biological applications as an alternative therapy for disease conditions utilizing the nanobiotechnology domain for synthesis. The current study was performed to examine the antioxidant, anticancer, antibacterial, and antifungal potential of biosynthesized silver nanoparticles (TpAgNPs) using plant extract. The TpAgNPs were produced by reacting the Tradescantia pallida extract and AgNO3 solution in nine various concentration ratios subjected to bioactivities profiling. According to the current findings, plant extract comprising phenolics, flavonoids, and especially anthocyanins played a critical role in the production of TpAgNPs. UV-visible spectroscopy also validated the TpAgNP formation in the peak range of 401-441 nm. Further, the silver ion stabilization by phytochemicals, face-centered cubic structure, crystal size, and spherical morphology of TpAgNPs were analyzed by FTIR, XRD, and SEM. Among all TpAgNPs, the biosynthesized TpAgNP6 with a medium concentration ratio (5:10) and the plant extract had effective antioxidant potentials of 77.2 ± 1.0% and 45.1 ± 0.5% free radical scavenging activity, respectively. The cytotoxic activity of TpAgNP6 in comparison to plant extract for the rhabdomyosarcoma cell line was significantly the lowest with IC50 values of 81.5 ± 1.9 and 90.59 ± 1.6 µg/ml and cell viability % of 24.3 ± 1.62 and 27.4 ± 1.05, respectively. The antibacterial and antifungal results of TpAgNPs revealed significant improvement in comparison to plant extract, i.e., minimum inhibition concentration (MIC) 64 µg/ml against Gram-negative Pseudomonas aeruginosa while, in the case of antifungal assay, TpAgNP6 was active against Candida parapsilosis. These TpAgNPs play a crucial role in determining the therapeutic potential of T. pallida due to their biological efficacy.

Promising Low-Cost Adsorbent from Waste Green Tea Leaves for Phenol Removal in Aqueous Solution.

Phenol is the most common organic pollutant in many industrial wastewaters that may pose a health risk to humans due to its widespread application as industrial ingredients and additives. In this study, waste green tea leaves (WGTLs) were modified through chemical activation/carbonization and used as an adsorbent in the presence of ultrasound (cavitation) to eliminate phenol in the aqueous solution. Different treatments, such as cavitation, adsorption, and sono-adsorption were investigated to remove the phenol. The scanning electron microscope (SEM) morphology of the adsorbent revealed that the structure of WGTLs was porous before phenol was adsorbed. A Fourier Transform Infrared (FTIR) analysis showed an open chain of carboxylic acids after the sono-adsorption process. The results revealed that the sono-adsorption process is more efficient with enhanced removal percentages than individual processes. A maximum phenol removal of 92% was obtained using the sono-adsorption process under an optimal set of operating parameters, such as pH 3.5, 25 mg L-1 phenol concentration, 800 mg L-1 adsorbent dosage, 60 min time interval, 30 ± 2 °C temperature, and 80 W cavitation power. Removal of chemical oxygen demand (COD) and total organic carbon (TOC) reached 85% and 53%. The Freundlich isotherm model with a larger correlation coefficient (R2, 0.972) was better fitted for nonlinear regression than the Langmuir model, and the sono-adsorption process confirmed the pseudo-second-order reaction kinetics. The findings indicated that WGTLs in the presence of a cavitation effect prove to be a promising candidate for reducing phenol from the aqueous environment.

Ligustrum lucidum Leaf Extract-Assisted Green Synthesis of Silver Nanoparticles and Nano-Adsorbents Having Potential in Ultrasound-Assisted Adsorptive Removal of Methylene Blue Dye from Wastewater and Antimicrobial Activity.

Present study was conducted to investigate the adsorption and ultrasound-assisted adsorption potential of silver nanoparticles (AgNPs) and silver nanoparticles loaded on chitosan (AgCS composite) as nano-adsorbents for methylene blue (MB) removal. AgNPs were synthesized using leaf extract of Ligustrum lucidum, which were incorporated on the chitosan's surface for modification. UV−Vis Spectroscopy, FTIR, XRD, SEM, and EDX techniques were used to confirm the synthesis and characterization of nanomaterials. Batch adsorption and sono-adsorption experiments for the removal of MB were executed under optimal conditions; for fitting the experimental equilibrium data, Langmuir and Freundlich's isotherm models were adopted. In addition, the antimicrobial potential of the AgNPs and AgCS were examined against selected bacterial and fungal strains. UV−Vis spectroscopy confirmed AgNPs synthesis from the leaf extract of L. lucidum used as a reducer, which was spherical as exposed in the SEM analysis. The FTIR spectrum illustrated phytochemicals in the leaf extract of L. lucidum functioning as stabilizing agents around AgNPs and AgCS. Whereas, corresponding crystalline peaks of nanomaterial, including a signal peak at 3 keV indicating the presence of silver, were confirmed by XRD and EDX. The Langmuir model was chosen as an efficient model for adsorption and sono-adsorption, which exposed that under optimum conditions (pH = 6, dye initial concentration = 5 mg L−1, adsorbents dosage = 0.005 g, time = 120 min, US power 80 W), MB removal efficiency of AgNPs was >70%, using ultrasound-assisted adsorption compared to the non-sonicated adsorption. Furthermore, AgNPs exhibited promising antibacterial potential against Staphylococcus aureus with the maximum zone of inhibition (14.67 ± 0.47 mm). It was concluded that the green synthesis approach for the large-scale production of metallic nanoparticles is quite effective and can be recommended for efficient and cost-effective way to eradicate dyes, particularly from textile wastewater.

Global genetic diversity and evolutionary patterns among Potato leafroll virus populations.

Potato leafroll virus (PLRV) is a widespread and one of the most damaging viral pathogens causing significant quantitative and qualitative losses in potato worldwide. The current knowledge of the geographical distribution, standing genetic diversity and the evolutionary patterns existing among global PLRV populations is limited. Here, we employed several bioinformatics tools and comprehensively analyzed the diversity, genomic variability, and the dynamics of key evolutionary factors governing the global spread of this viral pathogen. To date, a total of 84 full-genomic sequences of PLRV isolates have been reported from 22 countries with most genomes documented from Kenya. Among all PLRV-encoded major proteins, RTD and P0 displayed the highest level of nucleotide variability. The highest percentage of mutations were associated with RTD (38.81%) and P1 (31.66%) in the coding sequences. We detected a total of 10 significantly supported recombination events while the most frequently detected ones were associated with PLRV genome sequences reported from Kenya. Notably, the distribution patterns of recombination breakpoints across different genomic regions of PLRV isolates remained variable. Further analysis revealed that with exception of a few positively selected codons, a major part of the PLRV genome is evolving under strong purifying selection. Protein disorder prediction analysis revealed that CP-RTD had the highest percentage (48%) of disordered amino acids and the majority (27%) of disordered residues were positioned at the C-terminus. These findings will extend our current knowledge of the PLRV geographical prevalence, genetic diversity, and evolutionary factors that are presumably shaping the global spread and successful adaptation of PLRV as a destructive potato pathogen to geographically isolated regions of the world.

In-vitro and In-vivo management of Meloidogyne incognita (Kofoid and White) Chitwood and Rhizoctonia bataticola (Taub.) Butler in cotton using organic's.

Root-knot nematodes Meloidogyne incognita (Kofoid and White) Chitwood and Rhizoctonia bataticola (Taub.) Butler, fungus, are very dangerous root damaging pathogens. Present study was planned to establish a chemical control of these root deteriorating pathogens under lab conditions as well as in field. Maximum death rate of nematode juveniles and minimum numbers of nematode eggs hatched were recorded in plates treated with Cadusafos (Rugby® 100G) @12 g/100 ml and Cartap® (4% G) @9g/100 ml. Chemical treatment of Rhizoctonia bataticola with Trifloxystrobin + Tebuconazole (Nativo®) @0.2 g/100 ml and Mancozeb + Matalaxyl (Axiom) @0.25 g/100 ml significantly controlled the mycelial growth in plates. The best treatments tested in laboratory were applied in field as protective and curative treatments. Results proved that chemical control of root-knot nematode and root rot fungi by tested chemicals at recommended time and dose is a significant management technique under field conditions.

Photocatalytic degradation and kinetic modeling of azo dye using bimetallic photocatalysts: effect of synthesis and operational parameters.

Industrial wastewaters are the major source polluting the surface and ground water resources. Pollutants released along with the untreated textile industry wastewaters are responsible for the great damage to the natural resources like water. Considering the hazardous effects of the azo dyes (textile coloring agents) and their byproducts, there is a need to develop cost-effective and efficient treatment method for the textile wastewaters as such dyes have been reported as toxic, mutagenic, and carcinogenic and can cause direct demolition of aquatic communities. One of the possible and effective treatment methods is the use of TiO2 photocatalysis due to its chemical stability, low cost, and non-toxic nature. The present study explored the photocatalytic potential of anatase-type of bimetallic Cu-Ni/TiO2 photocatalysts under visible light irradiation for possible photocatalytic degradation and mineralization of Methyl Orange (MO), as model azo dye. The focus was to correlate the synthesis (different calcination temperatures, phase composition of TiO2 either anatase or rutile, and metal ion loading in terms of concentration and composition (Cu:Ni)) and operational parameters (photocatalyst loading, pollutant concentration, and irradiation time) that were believed responsible for the enhanced photocatalytic performance. Blank experiments were carried out to check the effect of metal loading in comparison to bare TiO2 and effect of absence or presence of light and photocatalysts on MO photodegradation. Results obtained using bimetallic photocatalysts are promising as compared to bare TiO2 as 100% MO removal and ~ 90% %COD removal were obtained in 90 min of irradiation, obeying a pseudo-first-order kinetics with photocatalytic reaction via the Langmuir-Hinshelwood mechanism with a good linear fit. Photocatalysts synthesized using anatase TiO2 were reported with improved performance compared to rutile phase. It is evident that synthesis parameters influence photocatalyst performance directly. The higher rate constant (> 1) that proves the excellent adsorption capacity of the tested photocatalysts for tested pollutants on the surface may have a great prospective for photocatalytic water purification at neutral pH.

Titanium oxide-bacterial cellulose bioadsorbent for the removal of lead ions from aqueous solution.

In the current study, nanocomposites of bacterial cellulose (BC) and amorphous TiO2 were prepared and characterized. The nanocomposites were evaluated as adsorbent for the removal of lead (Pb) from aqueous solution. The different reactions conditions such as pH, equilibrium time, temperature, adsorbent dose and possible recycling of adsorbent were studied. The nanocomposites were characterized through X-ray diffraction (XRD), scanning electron microscopy (SEM) and Fourier transform infrared spectroscopy (FTIR). The characterization results confirmed the formation of nanocomposites. Moreover, BC modified with 3 wt% TiO2 showed best results for the removal of Pb ions from aqueous solution. TiO2-BC nanocomposites remove Pb in concentration of 100 mg/L with removal efficiency above 90% in 120 min at pH 7 and room temperature. The adsorbent was recycled, and no profound decrease of efficiency was observed till three cycles of use. Desorption studies were also carried out for the reusability of the adsorbent. The adsorbent was found efficient, stable and reusable for the removal of lead in environmental water samples.

Ultrasound-assisted adsorption of phenol from aqueous solution by using spent black tea leaves.

This study is conducted to examine the removal of phenol using spent black tea leaves (SBTL) by the process of ultrasound-assisted adsorption. The effect of different treatment processes, i.e., sonolysis, adsorption, and ultrasound-assisted adsorption, was investigated. The morphology of SBTL was studied using a scanning electron microscope (SEM), and the porous structure of the SBTL was identified before phenol was adsorbed onto the adsorbent. FTIR analysis of SBTL after adsorption showed the presence of an aliphatic band of carboxylic acids which depict degradation of the phenol molecule due to ultrasound-assisted adsorption. The experimental results showed that the hybrid process was found more effective for phenol removal (85%) as determined by a spectrophotometer. The optimum conditions of the reaction parameters were found as: phenol conc. = 25 mg L-1, pH = 3.5, time = 60 min, adsorbent dosage = 800 mg L-1, ultrasound power = 80 W, and operating temperature = 30 ± 2 °C. Chemical oxygen demand (COD) and total organic carbon (TOC) were found to be 78 and 39%, respectively. HPLC studies suggest nonselective oxidation of phenol resulting in by-products such as catechol and hydroquinone and finally carboxylic acids and CO2. In order to find reaction kinetics, different kinetic models, viz. pseudo-first- and pseudo-second-order models, were studied. The best fit to the isotherm models, i.e., Langmuir and Freundlich, was determined. It is concluded that phenol removal by the hybrid process follows the pseudo-second-order reaction kinetics and Langmuir isotherm model. In addition, thermodynamic studies revealed the nonspontaneous and exothermic nature of the phenol adsorption process.

Removal of reactive blue 19 dye by sono, photo and sonophotocatalytic oxidation using visible light.

An efficient sonophotocatalytic degradation of reactive blue 19 (RB 19) dye was successfully carried out using sulfur-doped TiO2 (S-TiO2) nanoparticles. The effect of various treatment processes that is sonolysis, photolysis, catalysis, sonocatalysis, photocatalysis, and sonophotocatalysis were investigated for RB 19 removal. S-TiO2 were synthesized in 1, 3 and 5 wt.% of sulfur by sol-gel process and characterized by X-ray diffraction (XRD) and scanning electron microscopy coupled with energy dispersive X-ray (SEM-EDX), UV-Visible diffuse reflectance spectra (DRS). The results confirm anatase phase of TiO2, porous agglomerate structure, and a red shift in the absorbance spectra of S-TiO2. The dye degradation was studied by using UV-Vis spectrophotometer at λ max=594 nm. The reaction parameters such as pH, catalyst dosage, initial dye concentration, ultrasonic power and effect of sulfur doping in different weight percent were studied to find out the optimum degradation conditions. Optimum conditions were found as: S-TiO2=5 wt.%, catalyst (S-TiO2 5 wt.%)=50mg, RB 19 solution concentration=20 mg L(-1), pH=3, ultrasound power=100 and operating temperature=25°C. The response of 5 wt.% S-TiO2 was found better than 1 and 3 wt.% S-TiO2 and other forms TiO2. The sonophotocatalysis process was superior to other methods. During this process the ultrasound cavitation and photocatalysis water splitting takes place which leads to the generation of OH. As reveled by the GCMS results the reactive blue 19 (20 mg L(-1)) was degraded to 90% within 120 min. The S-TiO2 sonophotocatalysis system was studied for the first time for dye degradation and was found practicable, efficient and cost effective for the degradation of complex and resistant dyes such as RB19.

Synergistic effects of combining ultrasound with the Fenton process in the degradation of Reactive Blue 19.

The decoloration of reactive dye C.I. Reactive Blue 19 (RB 19) using combined ultrasound with the Fenton process has been investigated. The effect of varying the concentrations of hydrogen peroxide and iron sulfate, initial pH, ultrasonic power, initial dye concentration and dissolved gas on the decoloration and degradation efficiencies was measured. Calibration of the ultrasound systems was performed using calorimetric measurements and oxidative species monitoring using the Fricke dosimeter and degradations were carried out with a 20 kHz probe type transducer at 2, 4, 6 and 8 W cm(-2) of acoustic intensity at 15, 25, 50 and 75 mg L(-1) initial dye concentrations. First order rate kinetics was observed. It was found that while the degradation rate due to ultrasound alone was slow, sonication significantly accelerated the Fenton reaction. While the results were similar to those reported for other dyes, the effects occurred at lower concentrations. The rate and extent of decoloration of RB 19 increased with rising hydrogen peroxide concentration, ultrasonic powers and iron sulfate concentration but decreased with increasing dye concentration. An optimum pH value of pH=3.5 was found. The rate of decoloration was higher when dissolved oxygen was present as compared with nitrogen and argon confirming the solution phase mechanism of the degradation.

Enhanced decomposition of reactive blue 19 dye in ultrasound assisted electrochemical reactor.

Textile industry effluents contain reactive dyes that may harm our receiving waters. A typical reactive blue (RB) 19 dye is frequently detected in significant concentrations in textile industry effluents. Such dyes have generally shown resistance to decomposition and tend to persist in the environment for long periods and multiply the impacts to water and environment. Therefore, the present investigation focused on high-rate decomposition of a typical reactive dye RB 19 under various ultrasound and electrochemical process conditions. The decomposition of un-hydrolyzed and hydrolyzed forms of reactive blue (RB) 19 dye by ultrasound assisted electrochemical process was investigated using various parameters including dye concentration, pH, ultrasonic frequency and reaction time. Reaction kinetics, organic carbon and mechanism for dye decomposition were determined using UV-Visible spectrophotometry, TOC (total organic carbon) analysis and gas chromatography-mass spectrometry (GC-MS). Almost complete 90% color removal and a maximum of 56% TOC removal for 50 mg L(-1) dye concentration of un-hydrolyzed RB 19 dye was achieved at an ultrasonic frequency of 80 kHz, pH of 8 after 120 min. GC-MS analysis showed that a sonoelectrochemical treatment of un-hydrolyzed RB 19 dye for 30 min resulted in the formation of products e.g. acetic acid, benzoic acid etc. with the complete removal of dye. For hydrolyzed dye, a treatment of 10 min was enough and the results were comparable with 30 min treatment of un-hydrolyzed dye. Kinetics of ultrasound assisted electrolysis showed that the dye decomposition followed 1st order. The ultrasound assisted electrolysis for dye decomposition and hence decolorization proved to be more effective and the total energy consumption reduced to half as compared with simple electrolysis/sonochemical decomposition. Therefore, ultrasound assisted electrolysis was found to be more effective technique for dye decomposition of an otherwise environmentally persistent reactive dye.

Thermal-pressure-mediated hydrolysis of Reactive Blue 19 dye.

The thermal-pressure-mediated hydrolysis rates and the degradation kinetics of environmentally persistent Reactive Blue (RB) 19 dye were studied. The dye decomposition was studied at 40-120 degrees C, pH 2-10, and atmospheric pressure range of 1-2 atm. The intermediates and end products formed during the degradation were identified using gas chromatography/mass spectrometry and a possible degradation pathway of RB 19 was proposed. The stability of the dye in aqueous solution was influenced by changes in pH. At pH 4, half-life was 2247.5 min at 40 degrees C and it reduced to 339.4 min when the temperature was increased to 120 degrees C. Acidic conditions were more conducive to enhance hydrolysis rate than basic ones as the decomposition was optimum at pH 4. The kinetic studies indicated that the rate of hydrolysis apparently followed first order reaction. A linear relationship was observed between hydrolysis rate of RB 19 dye and increasing temperatures and pressures. Overall, 23% dye decomposition occurred in 120 minutes at pH 4, 120 degrees C and pressure of 2 atm. Along with thermal-pressure, a combination of techniques like physico-chemical, biological, enzymatic etc. may be more suitable choice for the effective treatment of RB19 dye.

Evaluation of trace metals in tobacco of local and imported cigarette brands used in Pakistan by spectrophotometer through microwave digestion.

Uncontrolled exposure of active and passive smokers to trace metals causes increase in health risks. The primary objective of this study was to determine whether local and imported cigarette brands used in Pakistan, have elevated levels of metals or not. Six metals manganese (Mn), cobalt (Co), copper (Cu), cadmium (Cd), lead (Pb) and zinc (Zn) were determined in tobacco of twenty cigarette brands (local and imported) used in Pakistan by flame atomic absorption Spectrophotometry. To overcome contamination chances and for complete digestion of analytes a microwave digester was used. The analytical results showed highest concentration of Mn (84.78 microg/g dry weight), Cd (0.525 microg/g dry weight) and Zn (14.34 microg/g dry weight) metals in imported brands in relation to counterparts from the local brands. Certain elevated levels were observed for Co (3.344 microg/g dry weight), Pb (14.16 microg/g dry weight) and Cu (7.889 microg/g dry weight) metals in local brands. The inter-metal relationships in the tobacco of local and imported cigarette brands showed some integrated variation in the selected metal levels. In view of health risk associated with the above metals, there should be a strict quality control over monitoring of heavy metals during growing, processing and smoking of tobacco. Therefore, it is prudent to minimize exposure to toxic substances whenever possible because smoking and exposure to cigarette smoke is a confounder to be taken into account when carrying out epidemiological studies on human exposure to metals.