Soluble organic nitrogen in forest soils of northeast China

Soluble organic nitrogen （SON） is recognized as a sensitive indicator of soil nitrogen status. The present work was conducted in the temperate forests of northeast China where soils are typically characterized by high organic matter and high organic nitrogen content, and soil sampling was made in early spring just after the freeze-thaw period. The water extracted SON pools in the organic layer of forest soils were measured within the range from 156.0 mg·kg^-1 to 292.6 mg·kg^-1, a similar magnitude of salt solution extracted SON pools reported in literatures. However, the water soluble SON pools in 0-15 cm mineral soils in present study were much higher （3-10 times） than any other reports, ranging from 58.6 mg·kg^-1 to 125.2 mg·kg^-1. Water soluble SON varied markedly among the soils under different forests and at different sites. The SON in water extracts were positively and significantly correlated to soil organic matter and total nitrogen contents, but negatively correlated to microbial biomass nitrogen （MBN）. The reasons of the abnormally large SON pools and the negative correlations between SON and MBN in the 0-15cm mineral soils in this study were specially discussed.

Biodegradability of soil water soluble organic carbon extracted from seven different soils

Water soluble organic carbon （WSOC） is considered the most mobile and reactive soil carbon source and its characterization is an important issue for soil ecology study. A biodegradability test was set up to study WSOC extracted from 7 soils differently managed. WSOC was extracted from soil with water （soil/water ratio of 1：2, W/V） for 30 min, and then tested for biodegradability by a liquid state respirometric test. Result obtained confirmed the finding that WSOC biodegradability depended on the both land use and management practice. These results suggested the biodegradability test as suitable method to characterize WSOC, and provided useful information to soil fertility.

Effects of Soluble Organic N on Evaluating Soil N-Supplying Capacity

It is important to study the soluble organic N （SON） extracted during water-logged incubation for evaluating soil Nsupplying capacity. Soil initial SON and mineral N （Nmin）, cumulative soluble organic N and NH4＋-N in leachates during water-logged incubation, mineralization potentials of both easily decomposable N （ND） and resistant N （NR）, and their relationships with N uptake by crop in pot experiment were investigated by using 10 kinds of farmland soils with widely different physical and chemical properties on the Loess Plateau, China, and the effects of SON on evaluating soil Nsupplying capacity were studied. The results showed that the average content of initial SON （23.9 mg kg^-1） of 10 soils was 28.8% of initial total soluble N and 2.4% of soil total N. The percentage of cumulative SON in leaching total soluble N （118.1 mg kg^-1 was 46.4%, higher than the percentage of initial SON （28.8%）, and almost close to the percentage of cumulative NH4^＋-N in the leachates. ND had close correlation with total N, and the correlation coefficients were 0.92 （P 〈 0.01, excluding SON in estimating ND） and 0.88 （P 〈 0.01, including SON in estimating ND）, respectively. N mineralization potential and mineralization rate constant were different with the soil types. ND of Los-Orthic Entisols and Ust-Sandiic Entisols were lower than that of Eum-Orthrosols. Mineralization rate constant for the fast decomposable N-fraction （kD） decreased and the mineralization rate constant of resistant materials （kR） increased when SON was taken into account. Cumulative NH4^＋-N was a better evaluation index of soil N-supplying capacity, and it is not only suitable for the first season crops but also for two successive season crops. Cumulative SON alone was not a satisfactory index for the potential of mineralizable N. But it would be more accurate for ND in revealing the potential mineralizable N when SON was taken into account. Cumulative TSN, to some extent, could also be taken as an index for the potential mineralizable N. Cumulative NH4＋-N, total soluble N, and ND were good indexes for estimating soil potential mineralizable N, especially for soils of two successive season crops. And cumulative total soluble N and ND in evaluating the permanence of soil N-supply is of greater significance when SON was included.

Partitioning of water soluble organic carbon in three sediment size fractions:Effect of the humic substances

Water soluble organic carbon （WSOC） in sediments plays an important role in transference and transformation of aquatic pollutants. This article investigated the inherent mechanisms of how sediemnt grain size affect the partitioning coeffcient （k） of WSOC. Influences of NaOH extracted humic substances were particularly focused on. Sediments were sampled from two cross-sections of the middle Yellow River and sieved into three size fractions （〈 63 μm, 63-100 μm, and 100-300 μm）. The total concentration of WSOC in sediments （Cwsoc） and k were estimated using multiple water-sediment ratio experiments. Results showed that Cwsoc ranged from 0.012 to 0.022 mg/g, while k ranged from 0.8 to 3.9 L/kg. Correlations between the spectrum characteristics of NaOH extracted humic substances and k were analyzed. Strong positive correlations are determined between k and the aromaticity indicators of NaOH extracted humic substances in different sediment size fractions. Comparing with finer fractions （〈 63 μm）, k is higher in larger size fractions （63- 100 μm and 100-300 μm） related to higher aromaticity degree of NaOH extracted humic substances mostly. While negative relationship between k and the area ratio of fourier transform infrared spectroscopy （FT-IR） at 3400 and 1430 cm^-1 implied that the lowest k was related to the highest concentration of acidic humic groups in particles 〈 63 μm. WSOC in finer fractions （〈 63 μm） is likely to enter into pore water, which may further accelerate the transportation of aquatic contaminants from sediment to water.

Fluorescence characteristics of water soluble organic carbon in eastern China

Fluorescence excitation and average molecular weight of 46 water soluble organic matter (WSOC) samples extracted from 20 soil types in eastern China were determined. It was found all samples shared similar spectroscopy. A good linear relationship existed between total organic carbon and excitation in the range of 350 to 450 nm though the content of organic carbon and pH of the samples vary in a wide range. No significant correlation between relative excitation intensity and average molecular weight of WSOC and FA was found, but the partial correlation became significant with pH as the controlling factor for WSOC samples. The relative excitation intensity showed a general trend of increasing from south to north in the study area. The pH value might play an important role in regulating the fluorescent spatial variation of WSOC. S153 A

Increased light availability enhances tolerance against ocean acidification-related stress in the calcifying macroalga Halimedaopuntia

Although the adverse impacts of ocean acidification(OA)on marine calcifiers have been investigated extensively,the anti-stress capabilities regulated by increased light availability are unclear.Herein,the interactive effects of three light levels(30μmol photons/(m^(2)·s),150μmol photons/(m^(2)·s),and 240μmol photons/(m^(2)·s)combined with two pCO_(2)concentrations(400 ppmv and 1400 ppmv)on the physiological acclimation of the calcifying macroalga Halimeda opuntia were investigated using a pCO_(2)-light coupling experiment.The OA negatively influenced algal growth,calcification,photosynthesis,and other physiological performances in H.opuntia.The relative growth rate under elevated pCO_(2)conditions significantly declined by 13.14%−41.29%,whereas net calcification rates decreased by nearly three-fold under OA conditions.Notably,increased light availability enhanced stress resistance through the accumulation of soluble organic molecules,especially soluble carbohydrate,soluble protein,and free amino acids,and in combination with metabolic enzyme-driven activities,OA stress was alleviated.The carotenoid content under low light conditions increased markedly,and the rapid light curve of the relative electron transport rate was enhanced significantly by increasing light intensities,indicating that this new organization of the photosynthetic machinery in H.opuntia accommodated light variations and elevated pCO_(2)conditions.Thus,the enhanced metabolic performance of the calcifying macroalga H.opuntia mitigated OA-related stress.

Control of different occurrence types of organic matter on hydrocarbon generation in mudstones

Organic matter(OM) is preserved as different occurrences in mudstones, which can affect the hydrocarbon generation process. However, little research has focused on hydrocarbon generation as a function of different occurrences of OM. This study collected a suite of mudstones in the Dongying Sag, Bohai Bay Basin, and conducted Rock-Eval Ⅵ pyrolysis after Soxhlet extraction and Na_(2)S_(2)O_(8) oxidation, aiming to quantify the OM with different occurrences and figure out the contributions of each occurrence of OM to the hydrocarbon generation. There are three types of occurrences of OM: soluble organic matter(SOM),mineral-bound organic matter(MOM), and particulate organic matter(POM). MOM is the most abundant among the three occurrence types of OM. SOM and MOM are the main hydrocarbon precursors, and their hydrocarbon contributions alternate with different kerogen types and layers. Additionally, MOMcontributed hydrocarbons are numerous at shallow depths;SOM-contributed hydrocarbons mainly occur at deep depths;and POM-contributed hydrocarbons change little with depth. These results demonstrate that MOM should be the main hydrocarbon precursor in shallow formations and that SOM is the main hydrocarbon contributor at deep depths.

Effect of Diesel Fuel Composition on Exhaust Emissions

In this paper,the influence of aromatic content,one of main fuel properties,on diesel particulate emissions was studied at five steady-state operating conditions using a heavy-duty Perkins 4.236 engine.Detailed analysis of the particulate showed the presence of biologically active polynuclear aromatic hydrocarbons(PAH) in high concentration.Unburnt PAH in liquid fuel are identified to be the dominant source of particulate PAH.Diesel particulates are also considered a potential health hazard because of the presence of PAH in the SOF of the particulates and some of these PAH are known to be carcinogenic.

Soluble porous organic cages as homogenizers and electron-acceptors for homogenization of heterogeneous alloy nanoparticle catalysts with enhanced catalytic activity

The creation of ultrafine alloy nanoparticles(<5 nm) that can maintain surface activity and avoid aggregation for heterogeneous catalysis has received much attention and is extremely challenging.Here,ultrafine PtRh alloy nanoparticles imprisoned by the cavities of reduced chiral covalent imine cage(PtRh@RCC3) are prepared successfully by an organic molecular cage(OMC) confinement strategy,while the soluble RCC3 can act as a homogenizer to homogenize the heterogeneous PtRh alloy in solution.Moreover,the X-ray absorption near-edge structure(XANES) results show that the RCC3 can act as an electron-acceptor to withdraw electrons from Pt,leading to the formation of higher valence Pt atoms,which is beneficial to improving the catalytic activity for the reduction of 4-nitrophenol.Attributed to the synergistic effect of Pt/Rh atoms and the unique function of the RCC3,the reaction rate constants of Pt_(1)Rh_(16)@RCC3 are 49.6,8.2,and 5.5 times than those of the Pt_(1)Rh_(16)bulk,Pt@RCC3 and Rh@RCC3,respectively.This work provides a feasible strategy to homogenize heterogeneous alloy nanoparticle catalysts in solution,showing huge potential for advanced catalytic application.

可溶性有机正极的自碳化保证其在钠离子电池中的稳定应用

为了解决小分子有机正极在钠离子电池(SIBs)中的溶解问题,我们提出了一种有效的有机电极表面自碳化策略,并制备了新型可溶性小分子有机化合物NTCDI-DAQ对该策略进行验证.通过对惰性气氛下碳化温度和碳化时间的精确控制,在NTCDI-DAQ颗粒表面成功形成了厚度为30-40 nm的碳层,可在不影响NTCDI-DAQ电化学行为的前提下,有效消除其溶解问题.在半电池中,NTCDI-DAQ@C在1 A g^(-1)下循环10,000次后仍能保持155 mA h g^(-1)的优异放电容量.在使用Na_(3)Bi为负极的全电池中,NTCDI-DAQ@C可以提供高达245 mA h g^(-1)cathode的峰值放电容量,且在0.1 A g^(-1)下循环200次后仍保持了223 mA h g^(-1)的超稳定容量.据我们所知,NTCDI-DAQ@C是SIBs中最好的小分子有机正极之一,NTCDI-DAQ@C//Na_(3)Bi SIBs的卓越综合性能也可与目前最先进的SIBs相媲美.

An evaluation of the emission profile for two-wheelers at a traffic junction

Two-wheeler vehicles are an important mode of transportation in developing countries. However, the emissions from two-wheeler vehicles are significant. Urban two-wheeler vehicles with gasoline-fueled engines produce NOx and particulate matter emissions that affect urban air quality. During traffic light stops and programmed stops, for instance, pollutants are emitted and are dangerous to human health. In this experimental study, two-wheeler vehicles with different makes, technologies and engine capacities were tested for exhaust emissions including gravimetric and online measurements at different engine speeds and a no load condition at a simulated traffic junction. Gravimetric measurements were performed by collecting the particulate mass （at two engine speeds： 1500 and 2500 rpm） from a diluted engine-out exhaust on quartz filter paper. Next, these collected particulates were used to determine the presence of metals, as well as the benzene soluble organic fraction （BSOF）. The total particulate mass, BSOF and trace elements were slightly higher at a higher engine speed （2500 rpm）. Online measurements were performed by sampling the engine exhaust （at four engine speeds： 1500, 2000, 2500, and 3000rpm） and using online instruments to determine the particle number and size distribution, the particle-bound polyaromatic hydrocarbons （PAHs）, the gaseous emissions and the smoke opacity. Engines with higher cubic capacity emitted a higher concentration of nano-particles. The particle-bound PAH concentration increased as the engine speed increased, but this concentration was notably low for the highest engine speed tested （3000 rpm）. The regulated gaseous emissions increased as the engine speed increased for all vehicles.

Chemical characteristics and source apportionment of PM_(2.5) between heavily polluted days and other days in Zhengzhou, China

PM（2.5） samples were collected in Zhengzhou during 3 years of observation, and chemical characteristics and source contribution were analyzed. Approximately 96% of the daily PM（2.5） concentrations and annual average values exceeded the Chinese National Ambient Air Quality Daily and Annual Standards, indicating serious PM（2.5） pollution. The average concentration of water-soluble inorganic ions was 2.4 times higher in heavily polluted days（daily PM32.5 concentrations ＆gt; 250 μg/mand visibility ＆lt; 3 km） than that in other days, with sulfate, nitrate, and ammonium as major ions. According to the ratio of NO-3/SO2-4,stationary sources are still the dominant source of PM（2.5） and vehicle emission could not be ignored. The ratio of secondary organic carbon to organic carbon indicated that photochemical reactivity in heavily polluted days was more intense than in other days.Crustal elements were the most abundant elements, accounting for more than 60% of 23 elements. Chemical Mass Balance results indicated that the contributions of major sources（i.e., nitrate, sulfate, biomass, carbon and refractory material, coal combustion, soil dust,vehicle, and industry） of PM（2.5） were 13%, 16%, 12%, 2%, 14%, 8%, 7%, and 8% in heavily polluted days and 20%, 18%, 9%, 2%, 27%, 14%, 15%, and 9% in other days, respectively.Extensive combustion activities were the main sources of polycyclic aromatic hydrocarbons during the episode（Jan 1-9, 2015） and the total benzo[a]pyrene equivalency concentrations in heavily polluted days present significant health threat. Because of the effect of regional transport, the pollution level of PM（2.5） in the study area was aggravated.

Chemical characteristics of PM_(2.5) during haze episodes in the urban of Fuzhou,China

Atmospheric fine particles （PM2.5） were collected in this study with middle volume samplers in Fuzhou, China, during both normal days and haze days in summer （September 2007） and winter （january 2008）. The concentrations, distributions, and sources of polycyclic aromatic hydrocarbons （PAHs）, organic carbon （OC）, elemental carbon （EC）, and water soluble inorganic ions （WSIls） were determinated. The results showed that the concentrations of PM2.s, PAHs, OC, EC, and WSIIs were in the orders of haze 〉 normal and winter〉 summer. The dominant PAHs of PM2.s in Fuzhou were Fluo, Pyr, Chr, BbF, BkF, BaP, BghiP, and IcdP, which represented about 80.0% of the total PAHs during different sampling periods. The BaPeq concentrations of ^-~PAHs were 0.78, 0.99, 1.22, and 2.43 ng/m3 in summer normal, summer haze, winter normal, and winter haze, respectively. Secondary pollutants （SO42 , NO3 , NH4＊, and OC） were the major chemical compositions of PM2.5, accounting for 69.0%, 55.1%, 63.4%, and 64.9% of PM2.s mass in summer normal, summer haze, winter normal, and winter haze, respectively. Correspondingly, secondary organic carbon （SOC） in Fuzhou accounted for 20.1%, 48.6%, 24.5%, and 50.5% of OC. The average values of nitrogen oxidation ratio （NOR） and sulfur oxidation ratio （SOR） were higher in haze days （0.08 and 0.27） than in normal days （0.05 and 0.22）. Higher OC/EC ratios were also found in haze days （5.0） than in normal days （3.3）. Correlation analysis demonstrated that visibility had positive correlations with wind speed, and neg- ative correlations with relative humidity and major air pollutants. Overall, the enrichments of PM2.5, OC, EC, SO42 ,andNO3 promoted haze formation. Furthermore, the diagnostic ratios of IcdP/（IcdP ＋ BghiP）, lcdP/BghiP, OC/EC, and NO3 /SO42 indicated that vehicle exhaust and coal consumption were the main sources of pollutants in Fuzhou.

Water uptake of multicomponent organic mixtures and their influence on hygroscopicity of inorganic salts

The hygroscopic behaviors of atmospherically relevant multicomponent water soluble organic compounds（WSOCs） and their effects on ammonium sulfate（AS） and sodium chloride were investigated using a hygroscopicity tandem differential mobility analyzer（HTDMA） in the relative humidity（RH） range of 5%–90%. The measured hygroscopic growth was compared with predictions from the Extended-Aerosol Inorganics Model（E-AIM） and Zdanovskii–Stokes–Robinson（ZSR） method. The equal mass multicomponent WSOCs mixture containing levoglucosan, succinic acid, phthalic acid and humic acid showed gradual water uptake without obvious phase change over the whole RH range. It was found that the organic content played an important role in the water uptake of mixed particles.When organic content was dominant in the mixture（75%）, the measured hygroscopic growth was higher than predictions from the E-AIM or ZSR relation, especially under high RH conditions. For mass fractions of organics not larger than 50%, the hygroscopic growth of mixtures was in good agreement with model predictions. The influence of interactions between inorganic and organic components on the hygroscopicity of mixed particles was related to the salt type and organic content. These results could contribute to understanding of the hygroscopic behaviors of multicomponent aerosol particles.