Effect of ambient polycyclic aromatic hydrocarbons and nicotine on the structure of Aβ42 protein

● B[a]P, nicotine and phenanthrene molecules altered the secondary structure of Aβ₄₂. ● β-content of the peptide was significantly enhanced in the presence of the PAHs. ● Nicotine made stable cluster with Aβ₄₂ peptide via hydrogen bonds. ● Phenanthrene due to its small size, interfered with the Aβ₄₂ monomer more strongly. Recent studies have correlated the chronic impact of ambient environmental pollutants like polycyclic aromatic hydrocarbons (PAHs) with the progression of neurodegenerative disorders, either by using statistical data from various cities, or via tracking biomarkers during in-vivo experiments. Among different neurodegenerative disorders, PAHs are known to cause increased risk for Alzheimer’s disease, related to the development of amyloid beta (Aβ) peptide oligomers. However, the complex molecular interactions between peptide monomers and organic pollutants remains obscured. In this work, we performed an atomistic molecular dynamics study via GROMACS to investigate the structure of Aβ₄₂ peptide monomer in the presence of benzo[a]pyrene, nicotine, and phenanthrene. Interestingly the results revealed strong hydrophobic, and hydrogen-bond based interactions between Aβ peptides and these environmental pollutants that resulted in the formation of stable intermolecular clusters. The strong interactions affected the secondary structure of the Aβ₄₂ peptide in the presence of the organic pollutants, with almost 50 % decrease in the α-helix and 2 %–10 % increase in the β-sheets of the peptide. Overall, the undergoing changes in the secondary structure of the peptide monomer in the presence of the pollutants under the study indicates an enhanced formation of Aβ peptide oligomers, and consequent progression of Alzheimer’s disease.     

Considering science needs to deliver actionable science

Conservation practitioners, natural resource managers, and environmental stewards often seek out scientific contributions to inform decision-making. This body of science only becomes actionable when motivated by decision makers considering alternative courses of action. Many in the science community equate addressing stakeholder science needs with delivering actionable science. However, not all efforts to address science needs deliver actionable science, suggesting that the synonymous use of these two constructs (delivering actionable science and addressing science needs) is not trivial. This can be the case when such needs are conveyed by people who neglect decision makers responsible for articulating a priority management concern and for specifying how the anticipated scientific information will aid the decision-making process. We argue that the actors responsible for articulating these science needs and the process used to identify them are decisive factors in the ability to deliver actionable science, stressing the importance of examining the provenance and the determination of science needs. Guided by a desire to enhance communication and cross-literacy between scientists and decision makers, we identified categories of actors who may inappropriately declare science needs (e.g., applied scientists with and without regulatory affiliation, external influencers, reluctant decision makers, agents in place of decision makers, and boundary organization representatives). We also emphasize the importance of, and general approach to, undertaking needs assessments or gap analyses as a means to identify priority science needs. We conclude that basic stipulations to legitimize actionable science, such as the declaration of decisions of interest that motivate science needs and using a robust process to identify priority information gaps, are not always satisfied and require verification. To alleviate these shortcomings, we formulated practical suggestions for consideration by applied scientists, decision makers, research funding entities, and boundary organizations to help foster conditions that lead to science output being truly actionable.     

A multidecadal oscillation in precipitation and temperature series is pronounced in low flow series from Puget Sound streams

In Pacific Northwest streams, summer low flows limit water available to competing instream (salmon) and out-of-stream (human) uses, creating broad interest in how and why low flows are trending. Analyses that assumed linear (monotonic) change over the last ~60 years revealed declining low flow trends in minimally disturbed streams. Here, polynomials were used to model flow trends between 1929 and 2015. A multidecadal oscillation was observed in flows, which increased initially from the 1930s until the 1950s, declined until the 1990s, and then increased again. A similar oscillation was detected in precipitation series, and opposing oscillations in surface temperature, Pacific Decadal Oscillation, and Interdecadal Pacific Oscillation series. Multidecadal oscillations with similar periods to those described here are well known in climate indices. Fitted model terms were consistent with flow trends being influenced by at least two drivers, one oscillating and the other monotonic. Anthropogenic warming is a candidate driver for the monotonic decline, and variation in (internal) climatic circulation for the oscillating trend, but others were not ruled out. The recent upturn in streamflows suggests that anthropogenic warming has not been the dominant factor driving streamflow trends, at least until 2015. Climate projections based on simulations that omit drivers of multidecadal variation are likely to underestimate the range, and rate of change, of future climatic variation.     

Temporal trends in agricultural water use and the relationships to hydroclimatic factors in the High Plains aquifer region

The High Plains aquifer (HPA) is the primary water source for agricultural irrigation in the US Great Plains. The water levels in many locations of the aquifer have declined steadily over the past several decades because the rate of water withdrawals exceeds recharge, which has been a serious concern to the water resources management in the region. We evaluated temporal trends and variations in agricultural water use and hydroclimatic variables including precipitation, air temperature, reference evapotranspiration, runoff, groundwater level, and terrestrial water storage across the HPA region for different periods from 1985 to 2020 at the grid, county, or region scale. The results showed that water withdrawals decreased from 21.3 km³/year in 1985 to 18.2 km³/year in 2015, while irrigated croplands increased from 71,928 km² in 1985 to 78,464 km² in 2015 in the entire HPA. The hydroclimatic time-series showed wetting trends in most of the northern HPA, but drying and warming trends in the southern region from 1985 to 2020. The groundwater level time-series indicated flat trends in the north, but significant declining in the central and southern HPA. Trends in irrigation water withdrawals and irrigation area across the HPA were controlled by the advancement of irrigation systems and technologies and the management of sustainable water use, but also were affected by dynamical changes in the hydroclimatic conditions.     

非柔性连接石化储罐配管温差应力分析与对策

储罐配管在温差作用下产生热位移会导致管壁产生热应力，未采用柔性连接的配管由于热应力集中作用可能发生破漏。针对与石油化工储罐非柔性连接的配管的安全问题，应用ANSYS有限元分析软件模拟计算石化企业典型配管的热应力分布；根据不同类型配管的分析结果，提出了工程技术与管理方面的针对性安全措施。研究结果表明:温差效应对石化储罐配管热应力影响显著，随内外温差的增加，配管应力集中的区域增大，最大热应力值增大；补偿措施能够改善配管的柔性，降低配管应力；约束载荷限制配管热膨胀从而增大配管应力；三通管是多根配管接合的区域，这种复杂管道交汇处会形成明显应力集中。研究结果对于提高石油化工非柔性连接配管安全性有一定的指导意义。     

Enhanced debromination of 2,2′,4,4′-tetrabromodiphenyl ether (BDE-47) by zero-valent zinc with ascorbic acid

• Highly efficient debromination of BDE-47 was achieved in the ZVZ/AA system. • BDE-47 debromination by the ZVZ/AA can be applied to a wide range of pH. • AA inhibits the formation of (hydr)oxide and accelerates the corrosion of ZVZ. • Reduction mechanism of BDE-47 debromination by the ZVZ/AA system was proposed. A new technique of zero-valent zinc coupled with ascorbic acid (ZVZ/AA) was developed and applied to debrominate the 2,2′,4,4′-Tetrabromodiphenyl ether (BDE-47), which achieved high conversion and rapid debromination of BDE-47 to less- or non-toxic forms. The reaction conditions were optimized by the addition of 100 mg/L ZVZ particles and 3 mmol/L AA at original solution pH= 4.00 using the solvent of methanol/H₂O (v:v= 4:6), which could convert approximately 94% of 5 mg/L BDE-47 into lower-brominated diphenyl ethers within a 90 min at the ZVZ/AA system. The high debromination of BDE-47 was mainly attributed to the effect of AA that inhibits the formation of Zn(II)(hydr)oxide passivation layers and promotes the corrosion of ZVZ, which leads to increase the reactivity of ZVZ. Additionally, ion chromatography and gas chromatography mass spectrometry analyses revealed that bromine ion and lower-debromination diphenyl ethers formed during the reduction of BDE-47. Furthermore, based on the generation of the intermediates products, and its concentration changes over time, it was proposed that the dominant pathway for conversion of BDE-47 was sequential debromination and the final products were diphenyl ethers. These results suggested that the ZVZ/AA system has the potential for highly efficient debromination of BDE-47 from wastewater.     

呼吸效应对矿井封闭火区氧浓度的影响分析

为避免因火区封闭导致重大安全事故发生，通过采集某矿井1 d内3个不同监测点的大气压力变化情况，建立大气压力波动模型并分析计算，同时建立火区内外压差100，750 Pa情形下的氧浓度模型进而获得火区内侧氧气浓度因呼吸效应，在不同压差、体积大小火区、风阻、瓦斯涌出量、封闭时刻等多因素耦合影响下随时间的变化规律，以评估火区危险性。研究结果表明:井下大气随地面大气周期波动，封闭火区内、外侧之间的气压差因外界大气波动呈现16 h的余弦波动和8 h的线性波动周期变化；密闭质量好的火区具有更好地抗干扰性，内侧氧浓度的降低主要依靠瓦斯稀释；密闭质量差的火区，内侧氧浓度易受到火区涌出瓦斯、外界涌入大气双重影响；火区氧浓度在2%~12%之间波动，以至火区存在发生瓦斯爆炸的可能性；火区内外压差较大时，氧浓度波动变化幅度更大，危险作用持续时间更长。结合火区氧浓度波动模型，可有效地对矿井火区采取安全的防范措施，避免瓦斯爆炸事故发生。     

基于响应曲面法的遗煤自燃分析与研究*

为研究高瓦斯易自燃煤层不同供风量、高抽巷抽采流量、低抽巷抽采流量3因素对采空区自燃“三带”分布影响规律，选取阳煤五矿8406工作面为研究对象，在数值模拟研究基础上，采用Design Expert软件进行Box Behnken试验设计，构建采空区氧化升温带宽度在3因素、3水平条件下的二次回归响应曲面模型，并对不同条件下采空区氧化升温带宽度进行预测与分析。结果表明:二次回归方程P值为0.001 6，预测模型显著，模型的失拟项为0.606 3，不显著，回归方程具有统计学意义；当供风量为1 500~2 000 m3/min，低抽流量为450~650 m3/min，高抽流量为100~200 m3/min时，对氧化升温带宽度一次项重要度排序为C（高抽巷抽采流量）>A（供风量）>B（低抽巷抽采流量），二次项重要度排序为AC（供风量和高抽巷抽采流量）>AB（供风量和低抽巷抽采流量）>BC（低抽巷抽采流量和高抽巷抽采流量），且AB,AC,BC之间均无交互作用。     

不同类型活性炭处理废水中重金属离子的研究进展

重金属对人体的显著毒性和难降解的特性,使重金属水体污染成为全球性关注的环境问题。本文综述了重金属废水的危害、来源及常用处理方法,比较了不同类型活性炭处理废水中重金属离子的差异,阐述了不同类型活性炭处理技术的优势和特点,并对今后的重金属废水处理技术研究方向进行了展望。     

Experimental research of LNG accidental underwater release and combustion behavior

Evaluating potential hazards caused by accidental LNG release from underwater pipelines or vessels is a significant consideration in marine transportation safety. The aim of this study was to capture the dynamic behavior of LNG jet released under water and to analyze its vapor dispersion characteristics and combustion characteristics on the water surface during different release scenarios. Controlled experiments were conducted where LNG was jet released from a cryogenic storage tank. The dynamic process of LNG being jet released from orifices of different sizes and shapes, as well as the rising plume structure, were captured by a high-speed camera. The leakage flow rate and pipeline pressure were recorded by a flow meter and pressure gauge, respectively. The concentration distribution that emanated from the water surface was measured utilizing methane sensors in different positions with various wind speeds. The flame combustion characteristics of LNG vapor clouds, which immediately ignited upon the enclosed water tank, were also recorded. Additionally, the mass burning rate of the flame on the water surface was evaluated, and a new correlation between the ratio of flame length and width was established. The results indicated a large dimensionless heat release rate (Q*) and a continuous release flow rate in a limited burning area. This study could provide greater understanding of the mechanisms of LNG release and combustion behavior under water.