Toxic trespassers: Uncovering phthalates and organophosphate flame retardants in children's rooms and their health implications.

Organophosphate flame retardants (OPEs) and phthalates have garnered significant attention due to their widespread presence in indoor environments. Many recent investigations have reported extensive contamination of indoor dust, air, children's toys, and other environmental compartments with these chemicals. This research aimed to analyze OPEs and phthalates in air (PM10) and dust samples collected from the bedrooms of children (N = 30) residing in various households in Jeddah, Saudi Arabia. High mean levels (ng/g) of phthalates namely DEHP (1438600) and DnBP (159200) were found in indoor dust while TPhP (5620) was the major OPEs in indoor dust. Similarly, DEHP and DnBP were the predominant phthalates in PM10 samples, exhibiting mean levels of 560 and 680 ng/m3, respectively. However, TCPP was the main OPEs with average levels of 72 ng/m3 in PM10 samples. The majority of individual phthalates and OPEs were detected in 90-100 % of the dust samples, whereas in PM10 samples, their presence ranged from 25 % to 100 %. The concentrations of OPEs were notably greater than those of PBDEs and other BFRs previously reported in these samples, suggesting their broader use than alternative BFRs. The estimated long-term non-carcinogenic risk, hazardous index (HI) and daily exposure via dust for children was above threshold levels for DEHP. On the other hand, the cumulative risk of cancer was below the concerning levels. Further research is required to explore diverse groups of chemicals in indoor microenvironments particularly significant for children, such as kindergartens, primary schools, and their rooms at home.

Nanocellulose-Based Passivated-Carbon Quantum Dots (P-CQDs) for Antimicrobial Applications: A Practical Review.

Passivated-carbon quantum dots (P-CQDs) have been attracting great interest as an antimicrobial therapy tool due to their bright fluorescence, lack of toxicity, eco-friendly nature, simple synthetic schemes, and possession of photocatalytic functions comparable to those present in traditional nanometric semiconductors. Besides synthetic precursors, CQDs can be synthesized from a plethora of natural resources including microcrystalline cellulose (MCC) and nanocrystalline cellulose (NCC). Converting MCC into NCC is performed chemically via the top-down route, while synthesizing CODs from NCC can be performed via the bottom-up route. Due to the good surface charge status with the NCC precursor, we focused in this review on synthesizing CQDs from nanocelluloses (MCC and NCC) since they could become a potential source for fabricating carbon quantum dots that are affected by pyrolysis temperature. There are several P-CQDs synthesized with a wide spectrum of featured properties, namely functionalized carbon quantum dots (F-CQDs) and passivated carbon quantum dots (P-CQDs). There are two different important P-CQDs, namely 2,2'-ethylenedioxy-bis-ethylamine (EDA-CQDs) and 3-ethoxypropylamine (EPA-CQDs), that have achieved desirable results in the antiviral therapy field. Since NoV is the most common dangerous cause of nonbacterial, acute gastroenteritis outbreaks worldwide, this review deals with NoV in detail. The surficial charge status (SCS) of the P-CQDs plays an important role in their interactions with NoVs. The EDA-CQDs were found to be more effective than EPA-CQDs in inhibiting the NoV binding. This difference may be attributed to their SCS as well as the virus surface. EDA-CQDs with surficial terminal amino (-NH2) groups are positively charged at physiological pH (-NH3+), whereas EPA-CQDs with surficial terminal methyl groups (-CH3) are not charged. Since the NoV particles are negatively charged, they are attracted to the positively charged EDA-CQDs, resulting in enhancing the P-CQDs concentration around the virus particles. The carbon nanotubes (CNTs) were found to be comparable to the P-CQDs in the non-specific binding with NoV capsid proteins, through complementary charges, π-π stacking, and/or hydrophobic interactions.

A Novel Microwave Hot Pressing Machine for Production of Fixed Oils from Different Biopolymeric Structured Tissues.

A microwave hot pressing machine (MHPM) was used to heat the colander to produce fixed oils from each of castor, sunflower, rapeseed, and moringa seed and compared them to those obtained using an ordinary electric hot pressing machine (EHPM). The physical properties, namely the moisture content of seed (MCs), the seed content of fixed oil (Scfo), the yield of the main fixed oil (Ymfo), the yield of recovered fixed oil (Yrfo), extraction loss (EL), six Efficiency of fixed oil extraction (Efoe), specific gravity (SGfo), refractive index (RI) as well as chemical properties, namely iodine number (IN), saponification value (SV), acid value (AV), and the yield of fatty acid (Yfa) of the four oils extracted by the MHPM and EHPM were determined. Chemical constituents of the resultant oil were identified using GC/MS after saponification and methylation processes. The Ymfo and SV obtained using the MHPM were higher than those for the EHPM for all four fixed oils studied. On the other hand, each of the SGfo, RI, IN, AV, and pH of the fixed oils did not alter statistically due to changing the heating tool from electric band heaters into a microwave beam. The qualities of the four fixed oils extracted by the MHPM were very encouraging as a pivot of the industrial fixed oil projects compared to the EHPM. The prominent fatty acid of the castor fixed oil was found to be ricinoleic acid, making up 76.41% and 71.99% contents of oils extracted using the MHPM and EHPM, respectively. In addition, the oleic acid was the prominent fatty acid in each of the fixed oils of sunflower, rapeseed, and moringa species, and its yield by using the MHPM was higher than that for the EHPM. The role of microwave irradiation in facilitating fixed oil extrusion from the biopolymeric structured organelles (lipid bodies) was protruded. Since it was confirmed by the present study that using microwave irradiation is simple, facile, more eco-friendly, cost-effective, retains parent quality of oils, and allows for the warming of bigger machines and spaces, we think it will make an industrial revolution in oil extraction field.

Nanobiochar Associated Ammonia Emission Mitigation and Toxicity to Soil Microbial Biomass and Corn Nutrient Uptake from Farmyard Manure.

The unique properties of NB, such as its nano-size effect and greater adsorption capacity, have the potential to mitigate ammonia (NH3) emission, but may also pose threats to soil life and their associated processes, which are not well understood. We studied the influence of different NB concentrations on NH3 emission, soil microbial biomass, nutrient mineralization, and corn nutrient uptake from farmyard manure (FM). Three different NB concentrations i.e., 12.5 (NB1), 25 (NB2), and 50% (NB3), alone and in a fertilizer mixture with FM, were applied to corn. NB1 alone increased microbial biomass in soil more than control, but other high NB concentrations did not influence these parameters. In fertilizer mixtures, NB2 and NB3 decreased NH3 emission by 25% and 38%, respectively, compared with FM alone. Additionally, NB3 significantly decreased microbial biomass carbon, N, and soil potassium by 34%, 36%, and 14%, respectively, compared with FM. This toxicity to soil parameters resulted in a 21% decrease in corn K uptake from FM. Hence, a high NB concentration causes toxicity to soil microbes, nutrient mineralization, and crop nutrient uptake from the FM. Therefore, this concentration-dependent toxicity of NB to soil microbes and their associated processes should be considered before endorsing NB use in agroecosystems.

Phthalate esters and plastic debris abundance in the Red Sea and Sharm Obhur and their ecological risk level.

The abundance of plastic debris (PDs) and its correlation with phthalic acid esters (PAEs), a class of pollutants associated with plastics, is not well understood, although PDs have been reported in relation to the release and distribution of aquatic pollutants such as PAEs. Few studies have linked the distribution of these pollutants in seawater. The current study examined the abundance and relationship of PDs and PAEs in seawater from Sharm Obhur and the Red Sea. Estimates were also made of their ecological impacts. Sharm Obhur is a semi-enclosed bay on the eastern shore of the Red Sea, near Jeddah, Saudi Arabia, and is heavily impacted by human activities. Contaminants from Sharm Obhur may be transported into the deep waters of the Red Sea by the subsurface outflow. The PAEs concentrations in the study area ranged from 0.8 to 1224 ng/L. Among the six PAEs studied, diethyl phthalate (DEP) (22-1124 ng/L), di-n-butyl phthalate (DBP) (9-346 ng/L) and di (2-ethylhexyl) phthalate (DEHP) (62-640 ng/L) were the predominant additives detected across all the sampling sits. Whereas the other PAEs, dimethyl phthalate (DMP) (5-76 ng/L), benzyl butyl phthalate (BBP) (4-25 ng/L) and di-n-octyl phthalate DnOp (0.5-80 ng/L) were generally lower in most samples. The sum of the six analyzed PAEs (∑6 PAEs) was lower at Sharm Obhur (587 ± 82 ng/L) and in the Red Sea shelf (677 ± 182 ng/L) compared to the Red Sea shelf break (1266 ± 354 ng/L). This suggests that degradation and adsorption of PAEs were higher in Sharm Obhur and on the shelf than on the shelf break. In contrast, there was no difference in the abundance of PDs between Sharm Obhur (0.04 ± 0.02 PDs/m3), Red Sea shelf (0.05 ± 0.02 PDs/m3) and in the Red Sea shelf break (0.03 ± 0.1 PDs/m3). Polyethylene (32%) and polypropylene (8%) were dominant, mostly smaller than 5 mm2 (78%), with the majority consisting of white (52%) and black (24%) fragments (39%), fibers (35%) and films (24%). A positive correlation between PAE concentration and abundance of PDs, suggests either a common source or a causal link through leaching. The ecological risk of ∑4PAEs (DMP, DEP, DBP and DEHP) ranged from (0.20-0.78), indicating a low to moderate risk for the Red Sea. The pollution index of PDs ranged from (0.14-0.36), showing that the Sharm Obhur and both sites of Red Sea suffered relatively low pollution.

The effects of salinity, temperature, and UV irradiation on leaching and adsorption of phthalate esters from polyethylene in seawater.

In this study, the leaching of six phthalic acid esters (PAEs) from three common consumer plastics was investigated: low and high density polyethylene (LDPE, HDPE) and recycled polyethylene (RP). The effects of salinity, temperature, and ultraviolet irradiation (UVR) on leaching were investigated. The study of leaching of phthalates in aqueous environments in batch experiments is challenging due to their readsorption by the high hydrophobicity of PAEs, and there are no standard methods to study release processes. Here with the experiments, leaching (A) and spiking (B) using six PAEs to study the readsorption in the leaching process. PAEs were identified and quantified using GC-MS. Dibutyl phthalate (DBP) and benzyl butyl phthalate (DEHP) showed considerable leaching during the 5-day incubation: 14 ±â€¯1 to 128 ±â€¯14 and 25 ±â€¯2 to 79 ±â€¯5 ng/cm2, respectively, under UVR, corresponding approximately to (1.9-13%) and (12.4-22.4%) of the solvent extracted mass. The highest Kd values were measured for RP polymers (0.3-9.4), followed by LDPE (0.5-5.4) and HDPE (0.2-2.2) polymers. Thus, readsorption of PAEs at the surface removed 30-80% of the leached PAEs in the dissolved phase. For example in LDPE, the calculated total release of DBP was up to 54 ±â€¯4 ng/cm2, while the dissolved amount was 8.5 ±â€¯1 ng/cm2 during the 5-day incubation under freshwater conditions. Increasing salinity negatively affected the leaching rate, which decreased for DBP from 54 ±â€¯4 ng/cm2 in freshwater to 44 ±â€¯3 and 38 ±â€¯3 ng/cm2 at salinity of 20 and 40 g/L, respectively, from LDPE during the 5-day incubation. Temperature and UVR had a positive effect on the leaching rate, with the release of DBP from LDPE increasing from 44 ±â€¯3 ng/cm2 at room temperature (25 °C) to 60 ±â€¯6 and 128 ±â€¯14 ng/cm2 at high temperature (40 °C) and UVR, respectively. Overall, this study highlights the positive relationship between temperatures, UVR on the extent of leaching and surface adsorption on the leaching measurements.

The role of size-controlled CeO2 nanoparticles in enhancing the stability and photocatalytic performance of ZnO in natural sunlight exposure.

In order to enhance the photocatalytic performance and stability, the various proportions of the size controlled cerium oxide (CeO2) nanoparticles were dispersed at the pre-synthesized ZnO. Although, the expected dual absorption onsets, probably due to the diminutive difference between the bandgaps of CeO2 (∼2.9 eV) and ZnO (∼3.1 eV), were not observed however, a blue shift in the bandgap energy of ZnO was witnessed with the increasing surface density of CeO2 particles. The delayed excitons recombination process with the increasing concentration of CeO2 nanoparticles was verified by the PL spectra. The structural investigation by Raman and XRD analysis revealed the surface attachment of CeO2 particles without altering the rock-salt lattice of ZnO. The morphological and fine microstructural analysis established the uniform distribution of evenly sized CeO2 particles at the surface of ZnO with the discrete fringe patterns of both the entities whereas the XPS analysis confirmed the majority of Ce4+ in dispersed CeO2. In comparison to pure ZnO, cyclic voltammetric (CV) analysis, under illumination, exposed the supportive role of surface residing CeO2 particles in eradicating the photo-corrosion of ZnO whereas the chronopotentiometry (CP) predicted the prolonged life-span of the excitons. Compared to pure ZnO, an appreciably high activity was revealed for 10% CeO2 loading as compared to pure ZnO for the removal of mono and di-nitrophenol derivatives and their mixtures under natural sunlight exposure. The variations in the removal rates in the mixture as compared to individual nitrophenol exposed the structure-based priority of ROS for the respective phenol. The significantly enhanced photocatalytic activity of the composite catalysts revealed the incremental role of surface-mounted CeO2 entities in boosting the generation of ROS under sunlight irradiation. The experimental observations were correlated and compiled to establish the mechanism of the removal process.

Temperature, humidity and outdoor air quality indicators influence COVID-19 spread rate and mortality in major cities of Saudi Arabia.

There is an increasing evidence that meteorological (temperature, relative humidity, dew) and air quality indicators (PM2.5, PM10, NO2, SO2, CO) are affecting the COVID-19 transmission rate and the number of deaths in many countries around the globe. However, there are contradictory results due to limited observations of these parameters and absence of conclusive evidence on such relationships in cold or hot arid tropical and subtropical desert climate of Gulf region. This is the first study exploring the relationships of the meteorological (temperature, relative humidity, and dew) and air quality indicators (PM10,CO, and SO2) with daily COVID-19 infections and death cases for a period of six months (1st March to August 31, 2020) in six selected cities of the Kingdom of Saudi Arabia by using generalized additive model. The Akaike information criterion (AIC) was used to assess factors affecting the infections rate and deaths through the selection of best model whereas overfitting of multivariate model was avoided by using cross-validation. Spearman correlation indicated that exponentially weighted moving average (EWMA) temperature and relative humidity (R > 0.5, P < 0.0001) are the main variables affecting the daily COVID-19 infections and deaths. EWMA temperature and relative humidity showed non linear relationships with the number of COVID-19 infections and deaths (DF > 1, P < 0.0001). Daily COVID-19 infections showed a positive relationship at temperature between 23 and 34.5 °C and relative humidity ranging from 30 to 60%; a negative relationship was found below and/or above these ranges. Similarly, the number of deaths had a positive relationship at temperature ˃28.7 °C and with relative humidity ˂40%, showing higher number of deaths above this temperature and below this relative humidity rate. All air quality indicators had linear relationships with the number of COVID-19 infections and deaths (P < 0.0001). Hence, variation in temperature, relative humidity and air pollution indicators could be important factors influencing the COVID-19 spread and mortality. Under the current scenario with rising temperature and relative humidity, the number of cases is increasing, hence it justifies an active government policy to lessen COVID-19 infection rate.

Exposure to Phthalate and Organophosphate Esters via Indoor Dust and PM10 Is a Cause of Concern for the Exposed Saudi Population.

In this study, we measured the occurrence of organophosphate esters (OPEs) and phthalates in the settled dust (floor and air conditioner filter dust) and in suspended particulate matter (PM10) from different microenvironments (households (n = 20), offices (n = 10) and hotels (n = 10)) of Jeddah, Saudi Arabia. Bis (2-Ethylhexyl) phthalate (DEHP) was the major pollutant (contributing >85% of total chemicals burden) in all types of indoor dust with a concentration up to 3,901,500 ng g-1. While dibutyl phthalate (DBP) and DEHP together contributed >70% in PM10 (1900 ng m-3), which indicate PM10 as a significant source of exposure for DBP and DEHP in different Saudi indoor settings. Tris (1-chloro-2-propyl) phosphate (TCPP) was the major OPE in PM10 with a concentration of up to 185 ng m-3 and the occurrence of OPEs in indoor dust varied in studied indoor settings. The estimated daily intake (EDI) of studied chemicals via dust ingestion and inhalation of PM10 was below the reference dose (RfD) of individual chemicals. However, estimated incremental lifetime cancer risk (ILCR) with moderate risk (1.5 × 10-5) for Saudi adults and calculated hazardous index (HI) of >1 for Saudi children from DEHP showed a cause of concern to the local public health.

Synthesis, characterization and photocatalytic performance of W6+ impregnated g-C3N4 for the removal of chlorophenol derivatives in natural sunlight exposure.

The surface of the g-C3N4 was altered by impregnating W6+ ions that transformed to homogeneously coated oxide layer by a calcination process. An enhanced absorption and the suppressed de-excitation in the emission spectra, with the increasing W6+ loading, exposed the supporting role of the coated layer in extending the spectral response as well as the prolonged life span of excitons. The same was further supported by electrochemical impedance spectroscopy (EIS). The XRD and XPS analysis revealed the coated layer as highly crystalline pure phase monoclinic WO3 with the majority of impregnated tungsten ions in 6+ oxidation state respectively, whereas the FESEM and HRTEM analysis substantiated the uniformity of the coated layer with the interlayer spacing of the 0.369 nm. Additionally, the probable formation of individual WO3 nanoparticles or clusters was ruled out. The as-synthesized impregnated photocatalysts, in comparison to pure g-C3N4, were subjected to natural sunlight exposure for the photocatalytic removal of chlorophenol derivatives (2-CP, 3-CP, 4-CP, 2,3-DCP, 2,4-DCP, 2,4,6-TCP and PCP) that revealed the 5 wt% coating as the optimum level for significant removal. The progress of the photocatalytic process was monitored by periodic HPLC analysis whereas ion chromatography (IC) was used for the estimation of released ions. The mineralization capability of the as-synthesized W6+ coated catalysts was measured by the time scale TOC measurements. As the formation of intermediates was indicated in HPLC analysis, selected samples were subjected to GC-MS analysis for the identification of the nature of intermediates. The variable degree of removal of chlorophenol derivatives signified the role of the position and orientation of Cl group. The kinetics of the removal process was evaluated with the calculation of rate constants. The results extracted from the analytical tools and the associated band edge potentials were correlated to speculate the probable mechanism as well as the identification of major reactive oxygen species (ROS) involved in the removal process.

Comparing and Contrasting MERS, SARS-CoV, and SARS-CoV-2: Prevention, Transmission, Management, and Vaccine Development.

The COVID-19 pandemic is responsible for an unprecedented disruption to the healthcare systems and economies of countries around the world. Developing novel therapeutics and a vaccine against SARS-CoV-2 requires an understanding of the similarities and differences between the various human coronaviruses with regards to their phylogenic relationships, transmission, and management. Phylogenetic analysis indicates that humans were first infected with SARS-CoV-2 in late 2019 and the virus rapidly spread from the outbreak epicenter in Wuhan, China to various parts of the world. Multiple variants of SARS-CoV-2 have now been identified in particular regions. It is apparent that MERS, SARS-CoV, and SARS-CoV-2 present with several common symptoms including fever, cough, and dyspnea in mild cases, but can also progress to pneumonia and acute respiratory distress syndrome. Understanding the molecular steps leading to SARS-CoV-2 entry into cells and the viral replication cycle can illuminate crucial targets for testing several potential therapeutics. Genomic and structural details of SARS-CoV-2 and previous attempts to generate vaccines against SARS-CoV and MERS have provided vaccine targets to manage future outbreaks more effectively. The coordinated global response against this emerging infectious disease is unique and has helped address the need for urgent therapeutics and vaccines in a remarkably short time.

Recent Advances in Metal Decorated Nanomaterials and Their Various Biological Applications: A Review.

Nanoparticles (nanoparticles) have received much attention in biological application because of their unique physicochemical properties. The metal- and metal oxide-supported nanomaterials have shown significant therapeutic effect in medical science. The mechanisms related to the interaction of nanoparticles with animal and plant cells can be used to establish its significant role and to improve their activity in health and medical applications. Various attempts have been made to discuss the antibiotic resistance and antimicrobial activity of metal-supported nanoparticles. Despite all these developments, there is still a need to investigate their performance to overcome modern challenges. In this regard, the present review examines the role of various types of metal-supported nanomaterials in different areas such as antibacterial, antifungal, anticancer, and so on. Based on the significant ongoing research and applications, it is expected that metal-supported nanomaterials play an outstanding role not only in medical but also in other important areas.

A highly conductive thin film composite based on silver nanoparticles and malic acid for selective electrochemical sensing of trichloroacetic acid.

A highly conductive thin film composite based on silver nanoparticles (AgNPs) and malic acid (MA) was deposited on glassy carbon electrode (GCE) for the selective and sensitive electrochemical sensing of trichloroacetic acid (TCA). The casting solution containing MA functionalized AgNPs was employed as a precursor for the thermal deposition of the AgNPs integrated MA thin film composite onto the GCE surface. The uniform coverage of AgNPs within the thin film composite at GCE was obtained by field emission scanning electron microscopy (FESEM). A significantly high charge transfer resistance of the modified electrode (85.7â€¯Ω for AgNPs-MA/GCE in 2 mM [Fe(CN)6]3-/4- at a bias of +0.235 V as compared to bare GCE (38.01 Ω) verified the optimum coating of AgNPs-MA composite at the surface of the electrode. The AgNPs-MA composite deposited GCE revealed substantial electrocatalytic activity toward TCA reduction with significantly enhanced reduction current. The novel electrode manifested a linear square wave voltammetric (SWV) response over the concentration ranges of 0.1-2 (R2 = 0.9953) and 4-100 µM (R2 = 0.9969) with a limit of detection (LOD) and limit of quantification (LOQ) of 30 nM and 92.5 nM, respectively. The modified electrode exhibited an excellent long-term stability (30 days) with the retention of >95% of initial current. The selectivity of the proposed electrode for the determination of TCA was examined in the presence of dichloroacetic acid (DCA) and monochloroacetic acid (MCA) with the retention of high recovery percentages.

Antimicrobial and anticancer activities of silver nanoparticles synthesized from the root hair extract of Phoenix dactylifera.

There is a continuous rise in the rate of medicine consumption because of the development of drug resistance by microbial pathogens. In the last one decade, silver nanoparticles (AgNPs) have become a remarkable choice for the development of new drugs due to their excellent broad-spectrum antimicrobial activity. In the current piece of work, we have synthesized AgNPs from the root extract of Phoenix dactylifera to test their antimicrobial and anti-cancer potential. UV-visible spectra showed the surface plasmon resonance peak at 420 nm λmax corresponding to the formation of silver nanoparticles, FTIR spectra further confirmed the involvement of biological moieties in AgNPs synthesis. Moreover, XRD analysis showed the crystalline nature of AgNPs and predicted the crystallite size of 15 to 40 nm. Electron microscopy analyses confirmed their spherical shape. In addition, synthesized AgNPs was also found to control the growth of C. albicans and E. coli on solid nutrient medium with 20 and 22 mm zone of inhibition, respectively. The 100% potency at 40 µg/ml AgNPs concentration was observed against E. coli and C. albicans after 4 h and 48 h incubation respectively. Importantly, AgNPs were also found to decrease the cell viability of MCF7 cell lines in vitro with IC50 values of 29.6 µg/ml and could act as a controlling agent of human breast cancer. Based on our results, we conclude that biologically synthesized AgNPs exhibited multifunctional properties and could be used against human cancer and other infectious diseases.

Improvements in wheat productivity and soil quality can accomplish by co-application of biochars and chemical fertilizers.

The beneficial role of biochar is evident in most of infertile soils, however this is argued that increment in crop yield owing to biochar application does not always achieve in cultivated/fertile soils. The nutrient biochar believed to enhance crop yield and soil fertility than structural biochar that may offset the positive effect of chemical fertilizer on crop performance but improves soil structural properties. Therefore, we investigated the effect of biochars [produced from nutrient rich feedstocks like poultry manure (PMB) and farmyard manure (FMB) and structural feedstocks such as wood chips (WCB) and kitchen waste (KWB)], and chemical fertilizers (CF) when applied alone or in combination on soil chemical properties, wheat growth, yield and nitrogen uptake in a cultivated clay loam soil. Sole biochar treatments increased the total carbon and mineral nitrogen content that were 21 and 106% higher, respectively compared to control after 128days (P<0.001). Contrarily, sole biochars application did not increase wheat biological yield and N uptake compared to control (P>0.05) except PMB, the nutrient biochar (P<0.05). Compared to control, grain yield was 6 and 12% lower in WCB and FMB, respectively but not differed from KWB, PMB or WCB-CF. Conversely, co-application of biochars and CF treatments increased crop biological yield but the increment was the highest in nutrient biochars FMB or PMB (29 or 26%), than structural biochars WCB and KWB (15 and 13%), respectively (P<0.05). For N uptake, this increment varies between 16 and 27% and again nutrient biochar has significantly higher N uptake than structural biochars. Hence, nutrient biochars (i.e. PMB) benefited the soil fertility and crop productivity more than structural biochars. Therefore, for immediate crop benefits, it is recommended to use nutrient biochar alone or in combination with chemical fertilizer. Such practice will improve crop performance and the quality of cultivated soil.

Marinobacter lipolyticus from Red Sea for lipase production and modulation of silver nanomaterials for anti-candidal activities.

In this study, the bacterial strain CEES 33 was isolated from the coastal area of the Red Sea, Jeddah, Kingdom of Saudi Arabia. The bacterium isolate was identified and characterized by using biochemical and molecular methods. The isolate CEES 33 has been identified as Gram-negative rod shaped and cream pigmented spherical colonies. It also demonstrated a positive result for nitrate reduction, oxidase, catalase, citrate utilization, lipase and exopolysaccharide production. Strain CEES 33 was characterized at the molecular level by partial 16S rRNA sequencing and it has been identified as Marinobacter lipolyticus (EMBL|LN835275.1). The lipolytic activity of the isolate was also observed 2.105 nkatml-1. Furthermore, the bacterial aqueous extract was used for green synthesis of silver nanoparticles (AgNPs), which was further confirmed by UV-visible spectra (430 nm), XRD and SEM analysis. Moreover, the biological functional group that involved in AgNPs synthesis was confirmed by FTIR spectra. The biological activities of AgNPs were also investigated, which showed a significant growth inhibition of Candida albicans with 16 ± 2 mm zone of inhibition at 10 µg dose/wells. Therefore, bacterium Marinobacter lipolyticus might be used in future for lipase production and nanoparticles fabrication for biomedical application, to control fungal diseases caused by C. albicans.

Potent bactericidal activity of silver nanoparticles synthesized from Cassia fistula fruit.

We demonstrated one-step synthesis of silver nanoparticles (AgNPs) from Cassia fistula fruit extract and their antibacterial activity against E. coli and K. pneumoniae. Biogenic AgNPs were characterized by scanning electron microscopy, X-Ray diffraction and fourier transform infrared spectroscopy. Results confirmed spherical shaped AgNPs with an average crystallite size of ∼69 nm. Dose-dependent (0, 10, 20, 40 and 80 µg mL-1) growth kinetic studies showed 100% potency against E. coli (20 µg mL-1) and K. pneumoniae (80 µg mL-1) after 1 and 5 h, respectively. Surface morphology analysis revealed formation of groove/pits in the lysed cell membrane that eventually led to bacterial death.

Toxicity of iron oxide nanoparticles to grass litter decomposition in a sandy soil.

We examined time-dependent effect of iron oxide nanoparticles (IONPs) at a rate of 2000 mg kg-1 soil on Cynodon dactylon litter (3 g kg-1) decomposition in an arid sandy soil. Overall, heterotrophic cultivable bacterial and fungal colonies, and microbial biomass carbon were significantly decreased in litter-amended soil by the application of nanoparticles after 90 and 180 days of incubation. Time dependent effect of nanoparticles was significant for microbial biomass in litter-amended soil where nanoparticles decreased this variable from 27% after 90 days to 49% after 180 days. IONPs decreased CO2 emission by 28 and 30% from litter-amended soil after 90 and 180 days, respectively. These observations indicated that time-dependent effect was not significant on grass-litter carbon mineralization efficiency. Alternatively, nanoparticles application significantly reduced mineral nitrogen content in litter-amended soil in both time intervals. Therefore, nitrogen mineralization efficiency was decreased to 60% after 180 days compared to that after 90 days in nanoparticles grass-litter amended soil. These effects can be explained by the presence of labile Fe in microbial biomass after 180 days in nanoparticles amendment. Hence, our results suggest that toxicity of IONPs to soil functioning should consider before recommending their use in agro-ecosystems.

Zinc oxide nanoparticles affect carbon and nitrogen mineralization of Phoenix dactylifera leaf litter in a sandy soil.

We investigated the impact of zinc oxide nanoparticles (ZnO NPs; 1000mgkg-1 soil) on soil microbes and their associated soil functions such as date palm (Phoenix dactylifera) leaf litter (5gkg-1 soil) carbon and nitrogen mineralization in mesocosms containing sandy soil. Nanoparticles application in litter-amended soil significantly decreased the cultivable heterotrophic bacterial and fungal colony forming units (cfu) compared to only litter-amended soil. The decrease in cfu could be related to lower microbial biomass carbon in nanoparticles-litter amended soil. Likewise, ZnO NPs also reduced CO2 emission by 10% in aforementioned treatment but this was higher than control (soil only). Labile Zn was only detected in the microbial biomass of nanoparticles-litter applied soil indicating that microorganisms consumed this element from freely available nutrients in the soil. In this treatment, dissolved organic carbon and mineral nitrogen were 25 and 34% lower respectively compared to litter-amended soil. Such toxic effects of nanoparticles on litter decomposition resulted in 130 and 122% lower carbon and nitrogen mineralization efficiency respectively. Hence, our results entail that ZnO NPs are toxic to soil microbes and affect their function i.e., carbon and nitrogen mineralization of applied litter thus confirming their toxicity to microbial associated soil functions.