黄河口潮间带碱蓬湿地植物-土壤系统V和Co生物累积的季节变化

2008年5—11月,对黄河口滨岸潮滩不同表现型碱蓬(Suaeda salsa)(中潮滩碱蓬,MMS,S.salsa in middle marsh;低潮滩碱蓬,LMS,S.salsa in low marsh)湿地植物-土壤系统V和Co含量的季节动态及其生物累积特征进行了研究。结果表明:MMS和LMS湿地表层土壤中V或Co含量的季节变化差异明显,但同一种湿地土壤中V和Co含量的变化模式相似。MMS(或LMS)湿地土壤的V含量均明显高于Co含量,二者在生长季的变异系数分别为12.01%、12.35%(MMS)和4.08%、4.94%(LMS)。MMS和LMS湿地表层土壤V的地累积指数(I_(geo))大多介于1—2,处于轻度污染状况;Co的I_(geo)大多介于0—1之间,处于无污染到轻度污染状态。V和Co含量在MMS不同部分中整体表现为枯落物根叶茎(P0.05),而在LMS中表现为枯落物叶茎根(P0.001)。MMS和LMS不同器官的V或Co转移能力存在较大差异,前者V和Co的R/S(根茎比)、R/L(根叶比)和S/L(茎叶比)大多大于1,后者中两种元素的相应比值则大多小于1。MMS和LMS不同部分的V和Co累积系数(AF)整体均表现为AFVAFCo,前者分别为后者的0.31—1.32、0.12—5.56、0.08—1.23、0.38—0.65倍(MMS)和0.14—0.84、0.23—0.68、0.34—0.77、0.43—0.56倍(LMS)。研究发现,MMS和LMS湿地土壤中有机质和铁锰氧化物含量的差异是导致二者V和Co含量存在差异的关键因素,而两种碱蓬生理生态学特性、所处生境水盐条件以及V和Co在不同器官扮演生态功能的差异是导致二者植物体内V和Co转移、分配与生物累积差异的重要原因。随着该区潮间带石油开采强度及石油燃料使用的增加,湿地表层土壤的V和Co(特别是V)污染问题将会逐渐凸显,而LMS可用于未来受V污染湿地修复的备选物种。     

Ultrathin Co3O4 Layers with Large Contact Area on Carbon Fibers as High‐Performance Electrode for Flexible Zinc–Air Battery Integrated with Flexible Display

A facile and binder‐free method is developed for the in situ and horizontal growth of ultrathin mesoporous Co₃O₄ layers on the surface of carbon fibers in the carbon cloth (ultrathin Co₃O₄/CC) as high‐performance air electrode for the flexible Zn–air battery. In particular, the ultrathin Co₃O₄ layers have a maximum contact area on the conductive support, facilitating the rapid electron transport and preventing the aggregation of ultrathin layers. The ultrathin feature of Co₃O₄ layers is characterized by the transmission electron microscopy, Raman spectra, and X‐ray absorption fine structure spectroscopy. Benefiting from the high utilization degree of active materials and rapid charge transport, the mass activity for oxygen reduction and evolution reactions of the ultrathin Co₃O₄/CC electrode is more than 10 times higher than that of the carbon cloth loaded with commercial Co₃O₄ nanoparticles. Compared to the commercial Co₃O₄/CC electrode, the flexible Zn–air battery using ultrathin Co₃O₄/CC electrode exhibits excellent rechargeable performance and high mechanical stability. Furthermore, the flexible Zn–air battery is integrated with a flexible display unit. The whole integrated device can operate without obvious performance degradation under serious deformation and even during the cutting process, which makes it highly promising for wearable and roll‐up optoelectronics.     

E2F6在物理性低氧及化学性低氧诱导的凋亡中的表达特征

心肌细胞凋亡性死亡是低氧发生时的重要病理学特征,但低氧诱导的心肌细胞凋亡的调控机制尚未完全阐明.E2F6是E2F转录因子家族成员之一,我们新近的研究证实其具有抑制DNA损伤诱导的细胞凋亡作用.但是,E2F6是否参与了低氧诱导的心肌细胞凋亡的调控尚不清楚.在本研究中,我们初步探讨了E2F6在物理性低氧及化学性低氧模拟物诱导大鼠心肌细胞系H9c2细胞凋亡中的表达特征.结果表明:物理性低氧、化学性低氧模拟物去铁胺(desferrioxamine,DFO)和氯化钻(cobalt chloride,CoCl2)均能有效诱导H9c2细胞发生凋亡.在物理性低氧及CoCl2,诱导的H9c2细胞凋亡中,内源性E2F6 mRNA表达明显下调,但蛋白表达没有明显变化.而在DFO诱导的凋亡中,内源性E2F6 mRNA及蛋白表达均发生明显下调.这些结果提示,E2F6可能参与调控DFO模拟低氧诱导的H9c2细胞凋亡,而对物理性低氧及CoCl2,模拟低氧诱导的细胞凋亡敏感性较低.此外,DFO模拟低氧诱导的细胞凋亡机制可能与物理性低氧及CoCl2.模拟低氧诱导的细胞凋亡机制不同.     

THE HORMESIS OF THE GREEN MACROALGA ULVA FASCIATA WITH LOW‐DOSE 60COBALT GAMMA RADIATION1

Homogenous germlings of the marine macroalga Ulva fasciata D. (synonym, Ulva lactuca L.) were used to study hormesis effects in macroalgae grown under a low dose of ⁶⁰Co γ‐ray radiation. The results of this study are the first to confirm the effects of macroalgal hormesis. Here it was demonstrated that growth of U. fasciata germlings was promoted substantially under 15 Gy of ⁶⁰Co γ‐ray radiation, with an average increase of algal biomass of 47.43%. The levels of polysaccharides and lipids varied among the tested material and showed no effects from the ⁶⁰Co γ‐ray radiation. However, the amount of protein was higher in the irradiated algae than in the control; the highest protein content of the irradiated algae was 3.958% (dry weight), in contrast to 2.318% in nonirradiated samples. This technique was applied to a field algal mass culture, which decreased the harvest time from 90 to 60 d. The mass culture approach may facilitate the production of macroalgae under unstable weather conditions such as typhoons in the summer or strong waves in the winter. The mass‐cultured macroalgae could be used as a source of bioenergy through the fermentation of algal simple sugars that derived from polysaccharides to produce ethanol.     

Mesoporous TiO2 Beads Offer Improved Mass Transport for Cobalt‐Based Redox Couples Leading to High Efficiency Dye‐Sensitized Solar Cells

Overcoming ionic diffusion limitations is essential for the development of high‐efficiency dye‐sensitized solar cells based on cobalt redox mediators. Here, improved mass transport is reported for photoanodes composed of mesoporous TiO₂ beads of varying pore sizes and porosities in combination with the high extinction YD2‐o‐C8 porphyrin dye. Compared to a photoanode made of 20 nm‐sized TiO₂ particles, electrolyte diffusion through these films is greatly improved due to the large interstitial pores between the TiO₂ beads, resulting in up to 70% increase in diffusion‐limited current. Simultaneously, transient photocurrent measurements reveal no mass transport limitations for films of up to 10 μm thickness. In contrast, standard photoanodes made of 20 nm‐sized TiO₂ particles show non‐linear behavior in photocurrent under 1 sun illumination for a film thickness as low as 7 μm. By including a transparent thin mesoporous TiO₂ underlayer in order to reduce optical losses at the fluorine‐doped tin oxide (FTO)‐TiO₂ interface, an efficiency of 11.4% under AM1.5G 1 sun illumination is achieved. The combination of high surface area, strong scattering behavior, and high porosity makes these mesoporous TiO₂ beads particularly suitable for dye‐sensitized solar cells using bulky redox couples and/or viscous electrolytes.     

A novel phosphorescence sensor for Co2+ ion based on Mn‐doped ZnS quantum dots

N‐acetyl‐l ‐cysteine‐capped Mn‐doped ZnS quantum dots (QDs) were prepared by hydrothermal methods. It could emit phosphorescence at 583 nm with the excitation wavelength at 315 nm. The phosphorescence intensity of QDs could be quenched dramatically by increasing the concentration of Co²⁺ ion. The novel phosphorescence sensor based on N‐acetyl‐l ‐cysteine‐capped QDs was developed for detecting Co²⁺ ion with a linear dynamic range of 1.25 × 10^–6–3.25 × 10^–5 m . The limit of detection and RSD were 6.0 × 10^–8 m and 2.3%, respectively. Interference experiments showed excellent selectivity over numerous cations such as alkali, alkaline earth and transitional metal ions. The possible quenching mechanism was also examined by phosphorescence decays. The proposed phosphorescence method was further applied to the trace determination of Co²⁺ ion in tap and pond water samples with recoveries of 97.75–103.32%. Copyright © 2013 John Wiley & Sons, Ltd.     

Applicability of Heavy-Metal Phytoextraction in United Arab Emirates: An Investigation of Candidate Species

Phytoremediation of contaminated calcareous desert land in the United Arab Emirates has been investigated. Soils from 12 northern UAE sites, suspected of metal contamination, were acid-extracted and analyzed by ICP-OES for Co, Cr, Cu, Fe, Mn, Ni, Pb, and Zn. Twenty-two plants naturally growing at contaminated sites were sampled and analyzed for their uptake of Co, Cr, Cu, Mn, Ni, Pb, and Zn and eight commercially available plants, grown under controlled conditions, were also studied for their phytoextraction capabilities. The concentration of available Cr was found to be 1300 ± 150 mg/kg in the soil of the Ajman Industrial Zone and 80 ± 10 mg/kg of Pb was found at Bithna. Among the plants investigated, Portulaca oleracea and Iresine herbstii showed potential for Cr(VI) and Pb(II) accumulation, respectively, with bioconcentration factors (BCF) greater than unity. Atriplex halimus accumulated Co(II), Cr(III), and Cu(II) each with a BCF > 1.     

Properties of a cobalt-reactivated form of yeast alcohol dehydrogenase

Yeast alcohol dehydrogenase (Y-ADH) is a widely studied metal-enzyme for its well-known biotechnological importance. Although its structure has been extensively investigated, some topics still remain controversial (zinc content and role), and various attempts aiming at modifying its structure to improve its catalytic properties have been made. In this paper, a metal-substituted Y-ADH has been prepared in vitro, in which one Zn atom per molecule (only one of those directly involved in catalysis) has been substituted by one Co atom. The substitution was obtained through zinc removal by a chelating treatment (with Chelex 100) followed by cobalt insertion. The zinc content in the native enzyme was preliminarily evaluated (taking care to avoid contamination) to be 4.1±0.1 g-at./molecule. After cobalt substitution, the ratio Zn:Co in the enzyme results to be 3:1. The active Co-Y-ADH has been compared with the native enzyme: it has lower specific activity (about 50%) and lower substrate affinity but greater thermo-resistance and a pH stability in a wider range than the native Y-ADH. A similar behavior, as far as cobalt content, thermo-resistance and pH stability are concerned, but greater specific activity and substrate affinity, were shown by an in vivo-substituted Co-Y-ADH obtained in a previous study.