A systematic review of systematic reviews and meta-analyses of animal experiments with guidelines for reporting

To maximize the findings of animal experiments to inform likely health effects in humans, a thorough review and evaluation of the animal evidence is required. Systematic reviews and, where appropriate, meta-analyses have great potential in facilitating such an evaluation, making efficient use of the animal evidence while minimizing possible sources of bias. The extent to which systematic review and meta-analysis methods have been applied to evaluate animal experiments to inform human health is unknown. Using systematic review methods, we examine the extent and quality of systematic reviews and meta-analyses of in vivo animal experiments carried out to inform human health. We identified 103 articles meeting the inclusion criteria: 57 reported a systematic review, 29 a systematic review and a meta-analysis, and 17 reported a meta-analysis only. The use of these methods to evaluate animal evidence has increased over time. Although the reporting of systematic reviews is of adequate quality, the reporting of meta-analyses is poor. The inadequate reporting of meta-analyses observed here leads to questions on whether the most appropriate methods were used to maximize the use of the animal evidence to inform policy or decision-making. We recommend that guidelines proposed here be used to help improve the reporting of systematic reviews and meta-analyses of animal experiments. Further consideration of the use and methodological quality and reporting of such studies is needed.     

Mobilization of soil organic matter by complexing agents and implications for polycyclic aromatic hydrocarbon desorption

Complexing agents are frequently used in treatment technologies to remediate soils, sediments and wastes contaminated with toxic metals. The present study reports results that indicate that the rate and extent of soil organic matter (SOM) as represented by dissolved natural organic carbon (DNOC) and polycyclic aromatic hydrocarbon (PAH) desorption from a contaminated soil from a manufactured gas plant (MGP) site can be significantly enhanced with the aid of complexing agents. Desorption of DNOC and PAH compounds was pH dependent, with minimal release occurring at pH 2-3 and maximal release at pH 7-8. At pH-6, chelate solutions were shown to dissolve large amounts of humic substances from the soil compared to controls. The complexing agents mobilized polyvalent metal ions, particularly Fe and Al from the soil. Metal ion chelation may disrupt humic (metal ion)-mineral linkages, resulting in mobilization of SOM and accompanying PAH molecules into the aqueous phase; and/or reduce the degree of cross-linking in the soil organic matter phase, which could accelerate PAH diffusion.     

Photocatalytic activity of TiO2 films grown on different substrates

Titanium dioxide films were prepared on glass, indium-tin oxide (ITO) glass and p-type monocrystalline silicon and studied for the photocatalytic degradation of rhodamine B in an aqueous medium. Raman, AFM, and XPS spectroscopic investigations of these films indicated that microstructure of titanium oxide films were greatly affected by the substrate materials. Rutile was confirmed to be easily formed on the surface of ITO glass, and TiO2 tended to grow as closely packed particles that were elongated strips with an average size of 20 nm, and had lovely contrast with the perfectly round particles grown on p-type monocrystalline silicon. Charge transfer between the film and silicon substrate was verified by surface photovoltage spectra. This may be the real reason why the films grown on ITO glass and silicon substrates exhibit higher photocatalytic reactivity than the film on glass substrate. Moreover, the different surface properties also seem to be responsible for the different activity.     

A comparison of the environmental impact of pesticide multiresidues and their occurrence in river waters surveyed by liquid chromatography coupled in tandem with UV diode array detection and mass spectrometry

Twenty-two pesticides and metabolites selected on the basis of a regional priority list, were surveyed in surface river waters by high performance liquid chromatography coupled in tandem with UV diode array detection and mass spectrometry, after an off-line pre-concentration step. Pesticide concentrations ranged between 0.07 and 4.8 microg/l according to the compound and sampling period. Analytical results were linked to the environmental risk of pesticides, evaluated by their system investigation of risk by integration of score (SIRIS) rank.     

Accelerated remediation of pesticide-contaminated soil with zerovalent iron

High pesticide concentrations in soil from spills or discharges can result in point-source contamination of ground and surface waters. Cost-effective technologies are needed for on-site treatment that meet clean-up goals and restore soil function. Remediation is particularly challenging when a mixture of pesticides is present. Zerovalent iron (Fe0) has been shown to promote reductive dechlorination and nitro group reduction of a wide range of contaminants in soil and water. We employed Fe0 for on-site treatment of soil containing > 1000 mg metolachlor, > 55 mg alachlor, > 64 mg atrazine, > 35 mg pendimethalin, and > 10 mg chlorpyrifos kg(-1). While concentrations were highly variable within the windrowed soil, treatment with 5% (w/w) Fe0 resulted in > 60% destruction of the five pesticides within 90 d and increased to > 90% when 2% (w/w) Al2(SO4)3 was added to the Fe0. GC/MS analysis confirmed dechlorination of metolachlor and alachlor during treatment. Our observations support the use of Fe0 for ex situ treatment of pesticide-contaminated soil.     

Volatilization of heavy metals during incineration of municipal solid wastes

Incineration experiments with MSW, which had been impregnated with heavy metals, were presented to obtain information on the volatilization behavior of the elements cadmium (Cd), lead (Pb), and zinc (Zn) under different conditions. Experiments were carried out in a bubbling fluid bed system connected to a customized inductively coupled plasma optical emission spectroscopy(ICP-OES) for analyzing metals in the flue gas. The results indicated that the combustion temperature, the gas atmosphere, and the chlorine content in the flue gas could affect the volatilization behavior of heavy metals. In the fluidized bed combustion, a large surface area was provided by the bed sand particles, and they may act as absorbents for the gaseous ash-forming compound. Comparer with the metals Cd and Pb, the vaporization of Zn was low. The formation of stable compounds such as ZnO.Al2O3 could greatly decrease the metals volatilization. The presence of chlorine would enhance the volatilization of heavy metals by increasing the formation of metal chlorides. However, when the oxygen content was high, the chlorinating reaction was kinetically hindered, which heavy metals release would be delayed.     

Aerobic dechlorination of cis- and trans-dichloroethenes by some indigenous bacteria isolated from contaminated sites in Africa

IntroductionChlorinatedethenesareamongthemostcommoncontaminantsobservedingroundwatersystems (Bouwer,1994;McCarty,1994) .Thesecompoundsvaryinnumberofchlorinesubstituents,fromthemostchlorinated,terachloroethene (PCE ) ,tothemonochlorinatedvinylchloride (VC …     

土地利用和理化环境对莫比尔-亚拉巴马河系中水甲基汞含量的影响

最近我们对美国东南部地区许多水域系统肉食性鱼类身上可能造成健康危险的超标汞(Hg)含量进行了测量.根据从出版的有关汞的水地球化学的实验数据得出的假设,我们调查了某些自然和人为的条件对莫尔比-亚拉巴马河系(MARS)中现场甲基汞(MeHg)含量的影响.从不同类型的环境采集了水样,假设这些水样具有不同的水甲基汞含量,并分析了总汞(THg)和甲基汞浓度以及一些主要的地球化学参数.结果如下:①总的来说,莫比尔-亚拉巴马河系水域中的总汞浓度分布相当均匀,从0.2ng/L到6ng/L不等,表明除了地质来源外,大气沉降肯定是所研究的水系中汞输入的主要来源.②在具有可比较的总汞含量的地点,以甲基汞形式存在的汞部分在从莫比尔-亚拉巴马河系的沿岸平原部分采集的样品中的含量始终比从其他地质区域采集的样品中的高.③我们的现场观测证实了从实验室试验获得的结论,即:甲基汞在水域系统中的丰度与硫酸盐(但只是在较窄的浓度范围内)有关,以及与pH的减少相关,而与硝酸盐或磷酸盐均无直接的关系.④对单一场所生物区中汞的累积的调查表明,在总汞浓度较低但甲基汞/总汞之比较高的水域系统中,生物的汞含量可能超出安全界限.因此,即使水相没有显示出有汞严重富集的迹象,也可能存在对食鱼人群的潜在健康威胁.     

Are flocculants required in a flocculant process?

The effectiveness of solids abatement by pH increase was investigated using the jar test procedure with a bentonite tap water suspension and an urban wastewater and an oxidation pond effluent. The results indicated that, depending on the suspended particles and on the dissolved ions, pH values between 9.5 and 12 induced extensive solids elimination without adding any other chemical than a base, i.e. sodium hydroxide or lime. The major effective reactions are then the calcium carbonate precipitation and the magnesium hydroxide precipitation. Moreover, this process does not require a flocculation step but only a precipitation step where the particles are entrapped by sweep coagulation and adsorption-coagulation. A continuous reactor was operated with an oxidation pond effluent. A suspended solids concentration less than 30 mg/l was obtained by adjusting pH between 11 and 11.5 while the reactor was operated up to 20 m/h superficial upflow velocity corresponding to a residence time through the whole unit of only 5 minutes. The sludge settling velocity depends on pH and on the primary particles but a maximum settling velocity larger than 1 m/h is easily reached. The concentration factor is then about 100. Environmental policy implications of this technique are that it allows to significantly upgrade a stabilization pond effluent and can be used when a high pH situation is acceptable.