The objective of this article is to describe the effect of precipitation and temperature on the drought characteristics of Yunnan province in China. The rainfall and temperature data from 10 national meteorological stations in Yunnan province during 1969 to 2018 were used to investigate the spatial and temporal evolution of drought in Yunnan province and the difference of drought index based on Standardized Precipitation Index (SPI) and Standardized Precipitation Evapotranspiration Index (SPEI) at nearly 50a different time scales. The results showed that Yunnan province had a frequent alternation of drought and flood, and the larger the time scale, the gentler the SPI and SPEI changes. The recent 50a drought mainly occurred in 1980–1982, 1988–1990, 2003–2007, and 2010–2015, and there was continuous drought and the duration was prolonged. The changes of SPI and SPEI showed a downward trend in different seasons. The linear slopes of SPI and SPEI in spring, summer, autumn, and winter were − 0.0064, − 0.0088, − 0.0057 and − 0.0.0111, respectively, and the drought trend was the most serious in winter. Continuous spring drought occurred in 2009–2010 and 2012–2014. The SPEI values in 2009–2010 and 2012–2014 were − 0.80, − 0.64, − 0.75, − 1.23, and − 1.17, respectively. The spatial distribution of drought frequency in Yunnan province was greatly different, and its distribution rule was more in the north and east, less in the south and west. The drought frequency in Zhaotong (northeast Yunnan) was the highest at 36.53%, the drought frequency in Deqin and Lijiang (northwest Yunnan) were 33.11% and 33.28%, and the drought frequency in Kunming (central Yunnan) Lincang, Lancang, and Simao (southwest Yunnan) were 29.35%, 30.73%, 32.77%, and 28.35%, respectively. This study provided a scientific basis for revealing the spatial and temporal variation rules, evolution trends, regional drought, and drought impact assessment and risk management of drought in Yunnan province.

The present study aims to investigate the optimum condition of stationary diesel engine’s operating parameters to obtain better performance and emission level, where the diesel engine is fueled with different concentrations of soybean biodiesel (SB), water, and alumina (Al) nanoadditive. Taguchi method coupled with gray relational analysis has been implemented in this study to obtain the optimum concentration of SB, water, and Al nanoparticle, and statistical analysis of variance (ANOVA) is applied to obtain the individual response of operating parameters on overall engine performance and emission level. Various concentration of SB (10%, 20%, and 30%), water (10%, 20%, and 30%), and Al nanoparticle (50 ppm, 100 ppm, and 150 ppm) are mixed with base diesel (BD) by mechanical agitation and followed by an ultra-sonication process. The fuel properties are measured based on EN590 standards, and the experiments are conducted in a single-cylinder, four-stroke, natural aspirated stationary diesel engine based on an L₉ orthogonal array fuel combination. From the obtained gray relational co-efficient (GRC) and signal-to-noise (S/N) ratio, the optimum concentration of SB, water, and nanoadditive are identified as 20%, 10%, and 100 ppm, respectively, and a confirmation experiment has also been carried out to confirm the improvements at optimum condition. The ANOVA results imply that water concentration (WC) has the maximum influence on overall diesel engine’s performance and emission level followed by nanoparticle and SB concentrations. Overall, it can be concluded that the engine exhibits better performance and greener emissions at optimal condition.

Surplus phosphorus (P) above agronomic requirements can negatively affect the water status of connected surface and subsurface water bodies. The in situ stabilization of soil P through soil amendment has been recognized as an efficient way to reduce this environmental pressure. However, the mechanism of how P is stabilized during this process and how plant available P is affected are unknown. This can be achieved by sequential chemical extraction and synchrotron-based X-ray absorption near-edge structure (XANES) spectroscopy investigations. Therefore, in the present study, P-enriched calcareous and red soils were amended with alum, dolomite, and a 1:1 mixture of alum and dolomite (MAD) at a 20 g/kg soil rate, and soil properties and P fractions were measured after a 45-day period. Results showed that alum amendment significantly decreased CaCl₂-P and Olsen-P contents in calcareous and red soils when compared with dolomite. However, dolomite incorporation maintained relatively high P availability and even increased CaCl₂-P and Olsen-P contents by 1.32% and 40.5% in red soil, respectively, compared to control. Amendment with MAD was not as effectively as the alum in P stabilization. Sequential inorganic P extraction indicated that alum dominantly contributed labile P transformed to Al-P in both soils. P K-edge XANES spectroscopy measurements further explained that alum adsorbed phosphate in calcareous soil and precipitated phosphate as AlPO₄ in red soil. Results of P fractionation and Mehlich-3-extracted Ca showed that dolomite mainly adsorbed loosely bound P in calcareous soil and red soil. However, dolomite incorporation in red soil led to Al-P and Fe-P release. The P sorption isotherms showed that dolomite and alum increased soil P sorption maxima and decreased the degree of P saturation (DPS) in both soils, while dolomite declined the Langmuir bonding energy in red soil. Differences in P stabilization by alum and dolomite addition across soil types were closely related to their characteristics, and soil properties changed, especially soil pH.

In this work, hexavalent chromium adsorption onto LDPE and agave fiber composites coated with chitosan or cellulose was studied in batch experiments. Chemical modifications consisting in cross-linked chitosan, cross-linked chitosan xanthate, and cellulose xanthate were applied to the polysaccharide-coated sorbents in order to increase their stability and adsorption capacity. The sorbents were characterized in terms of morphology by scanning electron microscopy and their chemical composition was evaluated by infrared and nuclear magnetic resonance spectroscopies. The results showed that the adsorption kinetics followed the pseudo-second-order model in all cases (i.e., chemisorption as the rate-limiting step of the adsorption reaction). Moreover, the isotherms evidenced a monolayer adsorption on homogeneous sites described by the Langmuir model. The maximum adsorption capacity of 284.7 mg Cr(VI)/g was obtained for the cross-linked chitosan xanthate sorbent at pH 4 which represents an increase of 43% against the chitosan-coated sorbent (199.1 mg Cr(VI)/g). Besides, functionalized cellulose sorbent also increased its capacity from 84.5 to 106.0 mg Cr(VI)/g cellulose due to the xanthate group. Up to six adsorption-desorption cycles were completed for the case of functionalized chitosan sorbent, confirming that the stability was increased with the cross-linking and the material could be reused several times without losing its adsorption capacity. In the case of cellulose xanthate, only three adsorption cycles were completed. However, improvements were observed in the desorption capacity considering that it decreased below 20% after two cycles in the cellulose-coated sorbent.

Three representative earthen canals from urban, peri-urban, and rural-urban fringe of Sri Lanka were studied for a 2-year period against different seasons to capture insights important in ecological rehabilitation. Only the canal from rural-urban fringe showed a better water quality in wet season; elucidating, the impact of contaminated catchment runoff in the other canals. At a given sampling session, one or two peaks (relative maxima) were observed in urban and peri-urban canals for pollution representative parameters such as nitrate nitrogen and soluble reactive phosphorus. Those peaks were highly localised, an indication of poor advection. In general, two-dimensional variations of electrical conductivity and turbidity in dry season were uniform in urban and peri-urban canals, an indication of dominant molecular diffusion. This was further evidenced via physical models for different flow stages (low, high, and bankfull). Therefore, fate of contaminants had to be mainly governed by assimilation via sediments. However, grey water footprint analyses showed urban and peri-urban canals have over utilised the natural assimilation capacity of many water quality parameters by several folds. This study proved the importance of inducing attenuation by instream physical heterogeneity similar to natural streams or naturalised canals such as the canal from the rural-urban fringe of this study.

This study aims to investigate the long-run and causal effects of energy consumption, economic growth, urbanization, and trade openness on CO₂ emissions in Turkey using newly developed econometric techniques. To our best knowledge, there has been no study examining the relationship between CO₂ emissions, energy consumption, trade openness, urbanization, and economic growth in Turkey. Therefore, this study proposes to fill this gap in the literature. In this study, we use time series data covering the years between 1960 and 2015. To capture long-run effects, we used ARDL, FMOLS, and DOLS estimators, while wavelet coherence technique is used to explore causal effects among the variables. Our results reveal that (i) there is a long-run equilibrium relationship between CO₂ emissions and energy consumption, economic growth, urbanization, and trade openness; (ii) in the long-run, CO₂ emission in Turkey is significantly triggered by energy consumption, economic growth, and urbanization; and (iii) the results of the wavelet coherence–based causality test provide supportive evidence to the long-run estimations of this study.

Magnetic Fe₃O₄ assembled on nanoscale zero-valent iron (nZVI) supported on an activated carbon fiber (ACF) to form nanoscale magnetic composites (nZVI-Fe₃O₄/ACF) for removing Cr(VI) and Cu(II) from aqueous solution through a permeable reactive column was synthesized via an in situ reduction method. The nZVI-Fe₃O₄/ACF composites and the interaction between nZVI-Fe₃O₄/ACF and both Cr and Cu ions were characterized by field emission scanning electron microscopy (FESEM) with EDX, TEM, XRD, and XPS. Batch experiments were used to analyze the effects of main factors on Cr(VI) removal and investigate the simultaneous removal of Cr(VI) and Cu(II) through a permeable reactive column. The results indicated that the ACF and Fe₃O₄ can inhibit the agglomeration and enhance the dispersibility of nZVI, and Fe₃O₄ and nZVI displayed good synergetic effects. The removal efficiency of Cr(VI) improved with the increase amount of Fe₃O₄ in the nZVI-Fe₃O₄/ACF composites. With low initial concentration of Cr(VI) and acidic conditions, ~ 90% of 20.0 mg·L⁻¹ Cr(VI) in the solution was removed after 60 min. The removal of Cr(VI) was also affected by coexisting ions. The removal efficiency of 10.0 mg·L⁻¹ Cu(II) was ~ 100% after 45 min of reaction, and the presence of Cu(II) can accelerate the reduction of Cr(VI). The simultaneous removal mechanisms of Cr(VI) and Cu(II) by the nZVI-Fe₃O₄/ACF composites also were proposed.

The issues of heavy metal contamination in water sources have been increasing substantially along with the rapid pace of industrial revolution. Lead, particularly, is one of the heavy metals that received considerable attention lately due to its frequent detection in the environment and hazardous effects. Although conventional water treatment processes had been utilized for ages, it is still a challenge to remove lead in the treatment plant effectively. In line with the advancement of chemistry and nanotechnology, the study on hydroxyapatite (HAp) nanopowder made from fish waste (skin, bones, and scales) has brought to its beneficial use as an adsorbent for lead removal in water. This paper reviews on the sources, occurrences, and health effects of lead as well as the treatment of lead using HAp adsorbent for its removal in water.

The quantity, intensity, and quality of urban stormwater runoff are changing as a consequence of urbanization and climate change. Low impact development (LID) techniques (e.g., bioretention systems) are emerging to manage runoff quantity and quality. Street tree pits were used as bioretention units in Montreal, Canada. The concentration and mass flux of contaminants (Na, Cr, Ni, Cu, Zn, Cd, Pb) and dissolved organic carbon (DOC) were measured in soil solution samples from the tree pits. The soil organic matter (SOM) and the permeability of the area nearby the tree pit (sidewalk and front lawn) were tested. The SOM did not affect contaminant concentrations. However, tree pits with higher SOM reduced the mass flux of contaminants more than tree pits with lower SOM. Sidewalk permeability decreased the concentration and mass flux of contaminants observed (e.g., Na and Cr). The estimated water flux in the open part of the tree pit changed from 6.15 to 1.64 mm week⁻¹ from the less permeable units (absence of lawn + impermeable sidewalk) to the more permeable units (presence of lawn + permeable sidewalk). Urban runoff quality and quantity were locally affected by the tree pits. This indicates that the increase in surface permeability and SOM in street tree pits is advisable. Street tree pits have the potential as bioretention units to locally mitigate some of the impacts of urbanization. City planners could consider the use of street tree pits as bioretention units to help the management of urban runoff.

Organic carbon (OC) and elemental carbon (EC) were measured in 24 h fine particulate matter (PM₂.₅) samples collected from May 2015 to April 2016 at urban and rural sites in Nanchong, a rapidly urbanized but low-level industrialized city in the Sichuan Basin, China. The annual average PM₂.₅, OC, and EC concentrations at urban sites were 45.6–55.7, 8.5–11.5, and 2.8–3.4 μg m⁻³, respectively, which were similar to the corresponding values (48.3, 10.6, and 3.3 μg m⁻³) at the rural site. The PM₂.₅ concentrations displayed strong monthly variations, with the highest (78.8–105.0 μg m⁻³) in January or February. Likewise, daily OC and EC concentrations exhibited high values in October (only for OC) and December 2015 to February 2016. Correlation, positive matrix factorization, and concentration weighted trajectory analyses were combined to investigate the sources of carbonaceous aerosol. The results indicated that OC and EC were mainly from biomass burning (60.7% and 45.8%) and coal combustion (30.2% and 25.7%), followed by vehicle emissions and road dust. The enhanced emissions from residential coal and biofuel uses in winter and straw combustion in October contributed to higher concentrations of OC and EC during these months. The contributions of biomass burning to OC and EC were significantly higher at the rural site (69.2% and 51.8%) than urban sites (56.3–58.6% and 37.8–41.5%). In addition to local emissions, the high concentrations of OC and EC at Nanchong were also influenced by regional transport in the basin.