One-pot synthesis of Ca-based magnetic hydrochar derived from consecutive hydrothermal and pyrolysis processing of bamboo for high-performance scavenging of Pb(â ¡) and tetracycline from water.

Ca-based magnetic bamboo-derived hydrochar described as Ca-MBHC was synthesized by one-pot pyrolysis, and was applied to remediation of lead (Pb) and tetracycline (TC) polluted water. Characterizations not only attested the loading of CaCO3 and Fe0 onto the hydrochar, but also demonstrated the magnetism of Ca-MBHC. Adsorption kinetic experiments showed that the Ca-MBHC could eliminate Pb(II) and TC during a wide range of pH, and appeared rapid uptake equilibrium within 240 and 60 min for Pb(II) and TC, severally. Adsorption isotherm experiments showed that the Ca-MBHC possessed highest adsorption of 475.58 mg/g concerning Pb(II), and heterogeneous uptake of 142.44 mg/g for TC. Furthermore, the Ca-MBHC could achieve Pb(II) binding owing to complexation, reduction, ion exchange and electrostatic attraction, whereas the TC uptake might be related to π-π stacking reciprocities, pore filling and hydrogen bonding. Overall, the Ca-MBHC could be viewed as an excellent adsorbent for scavenging Pb(II) and tetracycline from water.

Long non-coding RNA XIST regulates ovarian cancer progression via modulating miR-335/BCL2L2 axis.

BACKGROUND: X inactivation-specific transcript (XIST) is the long non-coding RNA (lncRNA) related to cancer, which is involved in the development and progression of various types of tumor. However, up to now, the exact role and molecular mechanism of XIST in the progression of ovarian cancer are not clear. We studied the function of XIST in ovarian cancer cells and clinical tumor specimens. METHODS: RT-qPCR was performed to detect the expression levels of miR-335 and BCL2L2 in ovarian cancer cells and tissues. MTT and transwell assays were carried out to detect cell proliferation, migration, and invasion abilities. Western blot was performed to analyze the expression level of BCL2L2. The interaction between miR-335 and XIST/BCL2L2 was confirmed using a luciferase reporter assay. RESULTS: The inhibition of XIST can inhibit the proliferation invasion and migration of human ovarian cancer cells. In addition, the miR-335/BCL2L2 axis was involved in the functions of XIST in ovarian cancer cells. These results suggested that XIST could regulate tumor proliferation and invasion and migration via modulating miR-335/BCL2L2. CONCLUSION: XIST might be a carcinogenic lncRNA in ovarian cancer by regulating miR-335, and it can serve as a therapeutic target in human ovarian cancer.

Study on the community structure and function of anaerobic granular sludge under trichloroethylene stress.

Trichloroethylene (TCE) is one of the most common groundwater pollutants. It is carcinogenic, teratogenic, mutagenic and poses a serious threat to human health and the environment. Therefore, reducing the environmental toxicity of TCE is of great significance. Anaerobic sludge was cultured and acclimated in an upflow anaerobic sludge blanket (UASB) reactor in this study. The Chemical Oxygen Demand (COD) concentration of the influent was approximately 2500 mg L-1, and the TCE concentration of the influent ranged from 1.46 mg L-1 to 73 mg L-1. After biodegradation of the anaerobic microflora, the COD removal rate was approximately 85%, and the TCE removal rate was over 85%. The microbial community of anaerobic sludge was analysed by 16 S rDNA clone libray and 454 high-throughput sequencing. Through analysis of the sequencing results, we found that there were a variety of acid-forming bacteria, anaerobic dechlorinating bacteria, and methanogenic bacteria. Based on the analysis of microflora function, it was speculated that the TCE metabolic pathway took place in UASB reactors. Desulfovibrio and Syntrophobacter provided an anaerobic environment, and acid-forming bacteria metabolise organic compounds into hydrogen. With Dehalobacter and Geobacter, TCE as an electron acceptor is dechlorinated and reduced under the anaerobic environment, in which hydrogen acts as an electron donor. By this, we clarified the metabolic pathway for improving TCE bioremediation.

Microwave-assisted synthesis of ß-cyclodextrin functionalized celluloses for enhanced removal of Pb(II) from water: Adsorptive performance and mechanism exploration.

Herein, ß-cyclodextrin (ß-CD) was efficiently grafted onto rice husk-based celluloses using different cross-linking agents of epichlorohydrin (EPI) and glutaraldehyde (GA). By feat of microwave irradiation, the functionalization procedure was completed in 17 min, and the synthesized RHEPIMWß-CD and RHGAMWß-CD exhibited fast adsorption equilibrium for Pb(II) within 20 min, excellent monolayer adsorption capacities of 216.06 and 279.08 mg g-1 across an extensive pH scope of 3.0-6.0, unaffected affinity to Pb(II) during the existence of co-existing ions, superior reusability with over 81% and 87% of Pb(II) uptake sustained for four adsorption-desorption cycles. Thermodynamic parameters implied that the uptake process of Pb(II) occurred spontaneously (-ΔG0) with an endothermic characteristic (+ΔH0). Furthermore, electrostatic attraction and complexation were demonstrated to enhance the Pb(II) uptake onto the RHEPIMWß-CD and RHGAMWß-CD. In fix-bed columns, these two adsorbents also efficiently eliminated Pb(II) under various flow rates with experimental breakthrough curves well simulated by Thomas and Yoon-Nelson models. Significantly, the RHEPIMWß-CD and RHGAMWß-CD could effectively purify acid battery effluent containing Pb(II) for meeting regulatory requirement. Overall, the fast fabrication, excellent adsorption and recycling performance facilitate the development of tailored adsorbents for Pb(II) elimination in wastewater.

Microwave-assisted one pot synthesis of ß-cyclodextrin modified biochar for concurrent removal of Pb(II) and bisphenol a in water.

Herein, ß-cyclodextrin (ß-CD) functionalized rice husk-derived biochar (BC) was conveniently and fast synthesized via microwave (MW)-assisted one pot process, and employed for simultaneous elimination of bisphenol A (BPA) and plumbum (Pb). Profiting by microwave irradiation, the surface modification was implemented in 15 min and the prepared BCMW-ß-CD presented an excellent adsorption performance with a heterogeneous adsorption capacity of 209.20 mg/g for BPA and a theoretical monolayer uptake of 240.13 mg/g for Pb(II) in the mono-component system. Furthermore, the BCMW-ß-CD could simultaneously achieve efficient cleanup of BPA and Pb(II) through avoiding the competitive behaviors between them, which were due to the different adsorption mechanisms for Pb(II) (i.e. electrostatic attraction and complexation) and BPA (i.e. host-guest supramolecular and π-π interactions). Moreover, the adsorbed BPA and Pb(II) could be sequentially desorbed with mild decrease in the adsorption performance of BCMW-ß-CD even after five cycles in the Pb(II)-BPA multi-component system.

Simultaneously enhanced removal and stepwise recovery of atrazine and Pb(II) from water using ß-cyclodextrin functionalized cellulose: Characterization, adsorptive performance and mechanism exploration.

Heavy metals and pesticides often coexist in contaminated water, while their potential competition behaviors make the adsorptive removal more challenging. Thus, decorating an adsorbent with independent functional sites could be a promising alternative to radically prevent the competitive process for improving the adsorption performance. Herein, ß-cyclodextrin functionalized rice husk-based cellulose (ß-CD@RH-C) was designed and applied for synchronous removal of atrazine and Pb(II). The characterization results supported the successful grafting of ß-cyclodextrin onto the cellulose. The ß-CD@RH-C presented a pH-dependent adsorption performance for Pb(II) with a theoretical monolayer adsorption capacity of 283.00 mg/g, while was mostly unrelated to pH for atrazine adsorption with a heterogeneous uptake of 162.21 mg/g in the mono-component system. Most importantly, the ß-CD@RH-C could efficiently achieve simultaneous removal of atrazine and Pb(II) via avoiding their competitive behaviors, which was due to the different adsorption mechanisms for atrazine (i.e. host-guest interaction) and Pb(II) (i.e. complexation and electrostatic interaction). Moreover, the adsorbed atrazine and Pb(II) could be sequentially desorbed with slight decrease in the adsorption performance of ß-CD@RH-C even after four cycles in the atrazine-Pb(II) multi-component system. All these results suggested ß-CD@RH-C to be a tailored adsorbent with high-performance elimination of co-existing heavy metals and organic pollutants in water.

Enhancing the atrazine tolerance of Pennisetum americanum (L.) K. Schum by inoculating with indole-3-acetic acid producing strain Pseudomonas chlororaphis PAS18.

Atrazine as a kind of herbicide could cause damage to the sensitive plants. Though plant growth promoting rhizobacteria (PGPR) have been proven with the potential to enhance the resistance of plants against various abiotic stresses, whether it could alleviate phytotoxicity caused by atrazine is sill unclear. In present study, the effects of strain Pseudomonas chlororaphis PAS18, a kind of PGPR enable to produce indole-3-acetic acid (IAA), on the growth and physiological responses of Pennisetum americanum (L.) K.Schum seedlings were investigated under three different levels (0, 20 and 100 mg kg-1) of atrazine in pot experiment. The results suggest that strain PAS18 could alleviate the growth and physiological interference caused by 20 mg kg-1 of atrazine. Physiological analysis showed strain PAS18 could further decrease the damaged extent of photosystem II, superoxide radical level and malondialdehyde content of test plant via up-regulating psbA expression, enhancing superoxide dismutase activity and reducing atrazine accumulation in the test plant. Moreover, ion flux measurements suggest that IAA could alleviate the Ca2+ exflux state of the test plant which caused by atrazine stress. Hence, it is plausible that strain PAS18 could alleviate atrazine-induced stress to P. americanum by enhancing the photosystem II repair and antioxidant defense ability as well as balancing the Ca2+ flux.

Trichloroethylene inhibits nitrogen transformation and microbial community structure in Mollisol.

Trichloroethylene (TCE) is the most ubiquitous halogenated organic pollutant in the environment, it is one of the 129 priority control pollutants. In order to clarify the influence of TCE on microorganisms and nitrogen transformation in Mollisol is the core purpose of this study. Results showed that 10 mg kg-1 TCE is the concentration limit of ammonification in Mollisol. When the concentration of TCE reached 10 mg kg-1 and the effect lasted for over 7 days, the process of ammonia oxidation to nitric acid in Mollisol will be affected. TCE affected the process of nitrate (NO3-) transformation into nitrite (NO2-) by affecting the activity of nitrate reductase, thereby affected the denitrification process in soil. When the concentration of TCE is more than 10 mg kg-1 it reduced the ability of soil microorganisms to obtain nitrogen, thereby affecting soil nitrogen transformation. RDA (Redundancy analysis) showed that the activity of nitrate reductase and the number of nitrifying bacteria and denitrifying bacteria in soil was negatively correlated with the incubation of TCE. In addition, soil nitrate reductase, nitrite reductase, peroxidase activity, ammonifying bacteria, nitrifying bacteria and denitrifying bacteria were negatively correlated with TCE concentration. Beyond that PICRUSt (Phylogenetic Investigation of Communities by Reconstruction of Unobserved States) of functional gene structure depend on KEGG (Kyoto Encyclopedia of Genes and Genomes) showed that 20 mg kg-1 TCE significantly inhibited the metabolism of energy and other substances in Mollisol. Based on the above, it is found that TCE significantly affected nitrification and denitrification in Mollisol, thus the nitrogen transformation in Mollisol was affected by TCE contamination.

Complete metabolic study by dibutyl phthalate degrading Pseudomonas sp. DNB-S1.

The primary purpose of this study was to systematically explore the complete metabolic pathway and tolerance mechanism of strain DNB-S1 to dibutyl phthalate (DBP), and the effect of DBP on energy metabolism of DNB-S1. Here, DNB-S1, a strain of Pseudomonas sp. that was highly effective in degrading DBP, was identified, and differentially expressed metabolites and metabolic networks of DBP were studied. The results showed that the differentially expressed metabolites were mainly aromatic compounds and lipid compounds, with only a few toxic intermediate metabolites. It speculated that phthalic acid, salicylic acid, 3-hydroxybenzoate acid, 3-Carboxy-cis, cis-muconate, fumarypyravate were intermediate metabolites of DBP. Their up-regulation indicated that there were two metabolic pathways in the degradation of DBP (protocatechuate pathway and gentisate pathway), which had been verified by peak changes at 290 nm, 320 nm, 330 nm, and 375 nm in the enzymatic method. Also, aspartate, GSH, and other metabolites were up-regulation, indicating that DNB-S1 had a high tolerance to DBP and maintained cell homeostasis, which was also one of the essential reasons to ensure the efficient degradation of DBP. Altogether, this study firstly proposed two pathways to degrade DBP and comprehensively explored the effect of DBP on the metabolic function of DNB-S1, which enriched the study of microbial metabolism of organic pollutants, and which provided a basis for the application of metabolomics.

Effects of trichloroethylene stress on the microbiological characteristics of Mollisol.

Trichloroethylene (TCE), one of 129 kinds of priority pollutants, is the most common halogenated organic pollutant in the environment. To explore the changes in soil physicochemical properties and biological activities then clarify the effects of these factors on bacterial, fungal and actinomycetes communities in Mollisol under TCE stress is the significance of our research. The results indicated that when TCE concentration was greater than 10 mg kg-1, soil quality declined and soil decomposition of organic matter and cycling of mineral nutrients were inhibited through an effect on soil microbial biomass. Operational taxonomic units (OTUs) richness of the bacteria in Mollisol was altered by TCE contamination. The SChao1 and HShannon indices of bacterial communities in Mollisol decreased when 40 mg kg-1 TCE was applied. Meanwhile, the OTU richness of fungi in Mollisol was altered by TCE contamination. The HShannon indices of the fungal communities in Mollisol were inhibited by higher TCE concentrations (20 and 40 mg kg-1 TCE). TCE altered the content of some bacteria, fungi and actinomycetes involved in soil carbon and nitrogen cycling and metabolism, such as Acidobacteria, Proteobacteria, Planctomycetes, Chytridiomycota, Streptomycetales, Pseudonocardiales, Propionibacteriales and Rhizobiales, and thus influenced nutrient cycling and the process of energy metabolism in Mollisol. In addition, redundancy analysis (RDA) results indicated that physicochemical properties and biological activities under TCE contamination significantly affected soil microbial community composition thus confirming that TCE interfered with the carbon and nitrogen cycling and metabolism of soil microorganisms. The results of this study are of great importance for revealing the effects of TCE stress on the microbiological characteristics of Mollisol, and also provide more useful information for determining the potential ecological risk of organic pollutants in Mollisol.

A combined system of microwave-functionalized rice husk and poly-aluminium chloride for trace cadmium-contaminated source water purification: Exploration of removal efficiency and mechanism.

Cadmium is highly poisonous to mammals and related water pollution incidents are increasing world-widely. Here, the clean-up of trace Cd(II) by a combined process of microwave-functionalized rice husk (RHMW-M) and poly aluminium chloride (PAC) was investigated for the first time, with the exploration of removal mechanism and efficacy. Microwave irradiation was found to be a new approach to achieve the functionalized procedure, which could decrease the processing time from 2.5 h to 390 s with the Cd(II) uptake of the outcome product soaring from 137.16 mg/g to 191.32 mg/g. The ultra-rapidly prepared RHMW-M exhibited a fast adsorption equilibrium within 30 min over a wide pH range of 5.0-8.0, and the FT-IR and XPS studies confirmed that both ion exchange and chelation were functioned in the Cd(II) uptake process. Controlled by the turbidity threshold of drinking water treatment plant, the feasible dosage of RHMW-M in the absence and presence of 30 mg/L PAC increased from 30 to 760 mg/L, which could effectively deal with the trace Cd(II) at the concentration from 33 µg/L up to 0.933 mg/L, exhibiting much better performance than traditional alkali precipitation. Predictably, this simple and scalable RHMW-M/PAC system could afford a promising end-of-pipe solution for heavy-metal contamination.

Potential therapeutic role of Co-Q10 in alleviating intervertebral disc degeneration and suppressing IL-1ß-mediated inflammatory reaction in NP cells.

Coenzyme Q10 (Co-Q10) is extraordinarily popular and has been used in abundant interventions as an antioxidant reagent that participates in numerous oxidation reactions. According to substantial evidence previously reported, interleukin-1ß (IL-1ß) is deemed to be one of the chief orchestrator molecules in the degeneration of intervertebral disc (IVD). However, it is unknown whether Co-Q10 is able to protect against IVD degeneration. In the current study, mouse-derived IVDs as well as primary human nucleus pulposus (NP) cells were isolated and cultured. NP cells were stimulated with IL-1ß, with or without selective addition of Co-Q10 to investigate the therapeutic effect of Co-Q10 on IVD degeneration. Levels of IL-1ß-induced inflammatory biomarkers including TNF-α, COX-2, IL-6 and iNOS were reduced by Co-Q10, which was possibly associated with inhibition of NF-κB signaling activation. Furthermore, Co-Q10 maintained the production of anabolic biomarkers in NP cells such as collagen 2, aggrecan and Sox-9 and altered the enhanced catabolism induced by IL-1ß. Moreover, the therapeutic role of Co-Q10 in sustaining IVD tissue-enhanced anabolism is potentially dependent on activation of the Akt signaling pathway. In summary, Co-Q10 may potentially represent an available molecular target that may shed light on approaches to the prevention and treatment of IVD degeneration in the future.

Investigating the behavior of binding properties between dissolved organic matter (DOM) and Pb(II) during the soil sorption process using parallel factor analysis (PARAFAC) and two-dimensional correlation spectroscopy (2D-COS).

Dissolved organic matter (DOM) is the most active component in an environmental system. It can influence the chemical and structural characteristics of soil. In this work, three-dimensional excitation-emission matrix (3D-EEM) fluorescence spectroscopy, parallel factor analysis (PARAFAC), and two-dimensional correlation spectroscopy (2D-COS) integrated with synchronous fluorescence were used to explore the interaction between soil-derived DOM and Pb(II) during the soil sorption process. According to the data of batch sorption experiments, the adsorbing capacities of soil, soil + 5 mL DOM, and soil + 10 mL DOM were 16.96, 18.29, and 19.32 mg g-1, respectively, which indicated that DOM significantly enhanced the adsorption efficiency of Pb(II). The pseudo-second-order kinetic equation could well explain the adsorption process. The adsorbing data conformed to the isotherm of Langmuir adsorption. According to EEM-PARAFAC results, there are two major components from DOM. Protein-like substances were represented by component 1, and humic-like and fulvic-like substances were represented by component 2. Based on 3D-EEM, the results further showed that the intensities of component 1 and component 2 were obviously quenched with the increase of Pb(II) concentrations. The combined interpretations of the 2D-COS map for the DOM revealed that Pb(II) binding might occur sequentially in the order of humic-like fraction > protein-like fraction (346 > 282 nm). According to synchronous fluorescence spectra, static fluorescence quenching was the major process of quenching. Graphical abstract ᅟ.

Characterization of spectral responses of dissolved organic matter (DOM) for atrazine binding during the sorption process onto black soil.

This study was aim to investigate the interaction between soil-derived dissolved organic matter (DOM) and atrazine as a kind of pesticides during the sorption process onto black soil. According to the experimental data, the adsorption capacity of Soil + DOM, Soil and DOM were 41.80, 31.45 and 9.35 mg kg-1, separately, which indicated that DOM significantly enhanced the adsorption efficiency of atrazine by soil. Data implied that the pseudo-second-order kinetic equation could well explain the adsorption process. The adsorption isotherms (R2 > 0.99) had a satisfactory fit in both Langmuir and Freundlich models. Three-dimensional excitation-emission matrix (3D-EEM), synchronous fluorescence, two-dimensional correlation spectroscopy (2D-COS) and Fourier transform infrared spectroscopy (FT-IR) were selected to analyze the interaction between DOM and atrazine. 3D-EEM showed that humic acid-like substances were the main component of DOM. The fluorescence of DOM samples were gradually quenched with the increased of atrazine concentrations. Synchronous fluorescence spectra showed that static fluorescence quenching was the main quenching process. 2D-COS indicated that the order of the spectral changes were as following: 336 nm > 282 nm. Furthermore, the fluorescence quenching of humic-like fraction occurred earlier than that of protein-like fraction under atrazine surroundings. FT-IR spectra indicated that main compositions of soil DOM include proteins, polysaccharides and humic substances. The findings of this study are significant to reveal DOM played an important role in the environmental fate of pesticides during sorption process onto black soil and also provide more useful information for understanding the interaction between DOM and pesticides by using spectral responses.

Chronic Calcium Channel Inhibitor Verapamil Antagonizes TNF-α-Mediated Inflammatory Reaction and Protects Against Inflammatory Arthritis in Mice.

It is well established that the tumor necrosis factor-α (TNF-α) plays a dominant role in rheumatoid arthritis (RA). Calcium channel is recently reported to be closely associated with various inflammatory diseases. However, whether chronic calcium channel blocker verapamil plays a role in RA still remains unknown. To investigate the role of verapamil in antagonizing TNF-α-mediated inflammation reaction and the underlying mechanisms, bone marrow-derived macrophages (BMDM) cells were cultured with stimulation of TNF-α, in the presence or absence of verapamil. Inflammation-associated cytokines, including IL-1, IL-6, inducible nitric oxide synthase 2 (NOS-2), and cyclooxygenase-2 (COX-2), were assessed, and verapamil suppressed TNF-α-induced expression of inflammatory cytokines. Furthermore, collagen-induced arthritis (CIA) mice models were established, and arthritis progression was evaluated by clinical and histological signs of arthritis. Treatment of verapamil attenuated inflammation as well as joint destruction in arthritis models. In addition, activity of NF-kB signaling pathway was determined both in vitro and in mice arthritis models, and verapamil inhibited TNF-α-induced activation of NF-kB signaling both in vitro and in mice models. Collectively, chronic calcium channel blocker verapamil may shed light on treatment of inflammatory arthritis and provide a potential therapeutic instrument for RA in the future.

Analysis of trichloroethylene removal and bacterial community function based on pH-adjusted in an upflow anaerobic sludge blanket reactor.

The study reported the upflow anaerobic sludge blanket (UASB) reactor performance in treating wastewater containing trichloroethylene (TCE) and characterized variations of bacteria composition and structure by changing the pH from 6.0 to 8.0. A slightly acidic environment (pH < 7.0) had a greater impact on the TCE removal. Illumina pyrosequencing was applied to investigate the bacterial community changes in response to pH shifts. The results demonstrated that pH greatly influenced the dominance and presence of specific populations. The potential TCE degradation pathway in the UASB reactor was proposed. Importantly, the genus Dehalobacter which was capable of reductively dechlorinating TCE was detected, and it was not found at pH of 6.0, which presumably is the reason why the removal efficiency of TCE was the lowest (80.73 %). Through Pearson correlation analyses, the relative abundance of Dehalobacter positively correlated with TCE removal efficiency (R = 0.912). However, the relative abundance of Lactococcus negatively correlated with TCE removal efficiency according to the results from Pearson correlation analyses and redundancy analysis (RDA).

Trichloroethylene removal and bacterial variations in the up-flow anaerobic sludge blanket reactor in response to temperature shifts.

Trichloroethylene (TCE) degradation and the variations of bacteria composition and structure in the up-flow anaerobic sludge blanket (UASB) reactor were investigated by increasing the operating temperature from 20 to 40 °C. The influent was supplemented with 36.5 mg/L of TCE. There was a rise in the chemical oxygen demand (COD) removal efficiency from 20 to 35 °C and a decline when temperature enhanced to 40 °C. It reached maximum at 35 °C. In addition, TCE removal efficiency increased with temperature varying from 20 to 35 °C, and it dropped dramatically to 78.38 % at 40 °C, which presumably because the genus of Dehalobacter, a kind of bacteria with the ability to dechlorinate TCE to the corresponding chlorinated products, was not detected at 40 °C according to sequencing results. The Illumina MiSeq platform was adopted to explore the bacteria composition and structure in response to temperature shifts. The results indicated that temperature impacted greatly on the dominance and presence of specific populations at different taxonomic levels. Importantly, the class Dehalococcoidia was detected from 25 to 40 °C, in which there were many well-known Dehalococcoides sp. strains that were capable of complete dechlorination of TCE to ethene. It also suggested the potential function of the dominant genera (non-dechlorinating bacteria and dechlorinating bacteria) in the reactor.

Morphology and morphogenesis of Epistylis plicatilis ehrenberg, 1831 (Ciliophora, Peritrichia) from Wuhan, China.

A limnetic peritrichous ciliate, Epistylis plicatilis Ehrenberg, 1831, was collected from a freshwater ditch beside Moshan Hill, Wuhan, China. Its morphology, infraciliature, and morphogenesis were investigated based on specimens examined in vivo, following staining with protargol and by scanning electron microscopy. The characteristics of the Wuhan population of E. plicatilis are as follows: 1) colonial, each colony typically comprising 30-50 individuals, with a dichotomously branched, noncontractile stalk; 2) fully expanded zooids measure 90-155 × 30-50 µm in vivo; 3) a series of 6 or 7 conspicuous folds appear in the posterior region of the zooid when it contracts; 4) single horseshoe-shaped macronucleus oriented transversely; 5) single contractile vacuole located in peristomial region on dorsal wall of infundibulum; 6) myoneme system comprises 20-24 longitudinal fibers, peristomial disk fibers as a wreath-like net and peristomial ring fibers; 7) narrowly spaced transverse striations on the surface of the body; 8) infundibular polykineties 1 and 2 are three-rowed, infundibular polykinety 3 is two-rowed; and 9) stomatogenesis is of the buccokinetal type; in the new oral apparatus, infundibular polykineties 2 and 3, the haplokinety, and the germinal kinety all originate from the germinal kinety of the parental oral apparatus whereas the polykinety and infundibular polykinety 1 originate from the parental haplokinety. An improved diagnosis of E. plicatilis is supplied.

Characterization of H3PO4-treated rice husk adsorbent and adsorption of copper(II) from aqueous solution.

Rice husk, a surplus agricultural byproduct, was applied to the sorption of copper from aqueous solutions. Chemical modifications by treating rice husk with H3PO4 increased the sorption ability of rice husk for Cu(II). This work investigated the sorption characteristics for Cu(II) and examined the optimum conditions of the sorption processes. The elemental compositions of native rice husk and H3PO4-treated rice husk were determined by X-ray fluorescence (XRF) analysis. The scanning electron microscopic (SEM) analysis was carried out for structural and morphological characteristics of H3PO4-treated rice husk. The surface functional groups (i.e., carbonyl, carboxyl, and hydroxyl) of adsorbent were examined by Fourier Transform Infrared Technique (FT-IR) and contributed to the adsorption for Cu(II). Adsorption isotherm experiments were carried out at room temperature and the data obtained from batch studies fitted well with the Langmuir and Freundlich models with R (2) of 0.999 and 0.9303, respectively. The maximum sorption amount was 17.0358 mg/g at a dosage of 2 g/L after 180 min. The results showed that optimum pH was attained at pH 4.0. The equilibrium data was well represented by the pseudo-second-order kinetics. The percentage removal for Cu(II) approached equilibrium at 180 min with 88.9% removal.

Biosorption of Pb(2+) by Saccharomyces cerevisiae in static and dynamic adsorption tests.

This paper demonstrates the Pb(2+) adsorption capacity and adsorption rate of Saccharomyces cerevisiae by both static and dynamic testing to verify its feasibility as a heavy metal bio-absorbent in wastewater treatment. The static testing was divided into two parts. First, we tested S. cerevisiae by itself, and then we tested immobilized S. cerevisiae. In static testing of the non-immobilized S. cerevisiae, the Pb(2+) adsorption capacity and adsorption rate increased up to 6.52 mg/g and 52.94%, respectively, with time. After immobilization, the Pb(2+) adsorption capacity and adsorption rate reached 10 mg/g and 80%, respectively. In dynamic testing, the optimal saturated adsorption capacity of immobilized S. cerevisiae for Pb(2+) was 6.64 mg/g. In addition to the static and dynamic testing of adsorption capacity and rate, we used SEM imaging to analyze the mechanics of adsorption, and the images showed that the cell wall played the major roll in Pb(2+) adsorption.