Organic carbon and nitrogen isotopes in surface sediments from the western Arctic Ocean and their implications for sedimentary environments

Surface sediments from the Chukchi Sea and adjacent arctic deep sea were investigated for organic carbon and nitrogen isotopes （in δ13Corg and δ15Norg） as well as biogeni＇c silica （BSiO2）. δ13Corg and δ15Norg values of surface sediments in the study area fall between the end-member values of marine and terrestrial organic matter from the surrounding lands and seas, their variations reflect the changes of marine productivity and terrestrial supply in the study area. BSiO2 shows a similar distribution pattern with δ13Corg and δ15Norg, and can be used as an indicator of marine productivity. In the central-west Chukchi Sea and the Chukchi Rise, sediments have higher δ13Corg, δ15Norg and BSiO2 values, indicating the region has high marine productivity influenced by the nutrient-rich branches of the Pacific waters. In the coastal zone off northwestern Alaska, δ13Corg and δ15Norg values become lighter, indicating a weakening marine productivity and an increasing terrigenous supply due to the effects of the least nutrient-rich branch of the Pacific waters. In the north and the northeast of the study area （including the Chukchi Plateau, the Canada Basin and the Beaufort shelf）, δ13Corg, δ15Norg and BSiO2 have the lowest values, and the terrigenous organic matter becomes dominant in surface sediments because this region has the longest ice-covered duration, the least nutrient-rich seawater and the increasing supply of terrestrial materials from the Mackenzie River and the northern Alaska under the action of the clockwise Beaufort gyre. Because the subarctic Pacific waters are continuously discharged into the central basin of the Arctic Ocean through the study area, the nutrient pool in the Chukchi Sea can be considered as a typical open system, the ratio of δ15Norg to BSiO2 content show some tracers that the level of nutrient utilization is contrary to nutrient supply and marine productivity formed in seawater.

Sources of particulate organic matter in the Chukchi and Siberian shelves: clues from carbon and nitrogen isotopes

The stable isotopic composition(δ13C andδ15N)and carbon/nitrogen ratio(C/N)of particulate organic matter(POM)in the Chukchi and East Siberian shelves from July to September,2016 were measured to evaluate the spatial variability and origin of POM.Theδ13CPOC values were in the range of−29.5‰to−17.5‰with an average of−25.9‰±2.0‰,and theδ15NPN values ranged from 3.9‰to 13.1‰with an average of 8.0‰±1.6‰.The C/N ratios in the East Siberian shelf were generally higher than those in the Chukchi shelf,while theδ13C andδ15N values were just the opposite.Abnormally low C/N ratios(<4),lowδ13CPOC(almost−28‰)and highδ15NPN(>10‰)values were observed in the Wrangel Island polynya,which was attributed to the early bloom of small phytoplankton.The contributions of terrestrial POM,bloom-produced POM and non-bloom marine POM were estimated using a three end-member mixing model.The spatial distribution of terrestrial POM showed a high fraction in the East Siberian shelf and decreased eastward,indicating the influence of Russian rivers.The distribution of non-bloom marine POM showed a high fraction in the Chukchi shelf with the highest fraction occurring in the Bering Strait and decreased westward,suggesting the stimulation of biological production by the Pacific inflow in the Chukchi shelf.The fractions of bloom-produced POM were highest in the winter polynya and gradually decreased toward the periphery.A negative relationship between the bloom-produced POM and the sea ice meltwater inventory was observed,indicating that the net sea ice loss promotes early bloom in the polynya.Given the high fraction of bloom-produced POM,the early bloom of phytoplankton in the polynyas may play an important role on marine production and POM export in the Arctic shelves.

Sources and transformations of nitrite in the Amundsen Sea in summer 2019 and 2020 as revealed by nitrogen and oxygen isotopes

In this study,the nitrogen and oxygen isotope compositions of nitrite in the upper 150 m water column of the Amundsen Sea in the summer of 2019 and 2020 were measured to reveal the distribution and transformation of nitrite in the euphotic zone of the Southern Ocean.We found that primary nitrite maxima(PNMs)are widely present in the Amundsen Sea,where the depth of occurrence deepens from east to west and nitrite concentrations increases.Evidence from dual isotopes suggests that the formation of PNMs in all regions of the Amundsen Sea is dominated by ammonia oxidation.More importantly,the nitrogen and oxygen isotope compositions of nitrite in the Amundsen Sea mixed layer are abnormal,and their depth profiles are mirror symmetrical.Isotopic anomalies exhibit spatial variations,with central surface water having the lowest nitrogen isotope composition(−89.9‰±0.2‰)and western surface water having the highest oxygen isotope composition(63.3‰±0.3‰).Isotopic exchange reaction between nitrate and nitrite is responsible for these isotope anomalies,as both nitrogen and oxygen isotopes have large isotopic fractionation and opposite enrichment effects.This proves that isotopic exchange reaction operates extensively in different regions of the Amundsen Sea.Our study highlights the unique role of dual isotopes of nitrite in deepening the understanding of nitrogen cycle.Further studies on ammonia oxidation and isotopic exchange between nitrate and nitrite are warranted in the future to understand their roles in the nitrogen cycle in the Southern Ocean.

The Marine Redox Change and Nitrogen Cycle in the Early Cryogenian Interglacial Time: Evidence from Nitrogen Isotopes and Mo Contents of the Basal Datangpo Formation, Northeastern Guizhou, South China

Cryogenian Datangpo Formation was deposited during the interglacial time between the Sturtian and Marinoan ice ages. We studied nitrogen isotope compositions and contents of Mo of the black shales from the basal Datangpo Formation in northeastern Guizhou, South China, for an attempt to reconstruct the marine redox change and nitrogen cycle during the interglacial time. Based on lithostratigraphy as well as geochemical profiles, the basal black shales can be divided into four intervals： Interval 1 has the lowest δ^（15）N value（＋5.0‰）; in interval 2, δ^（15）N values vary between ＋6.4‰ and ＋7.4‰（the first peak）; interval 3 records stable values of δ^（15）N around ＋6‰; and interval 4 is characterized by its higher δ^（15）N values, between ＋6.7‰ and ＋7.8‰（the second peak）. The values of enrichment factor of Mo decrease from 56.8 to 2.6 with the ascending stratigraphic trend. It indicated that immediately after the Sturtian glaciations, the marine seawater above the transitional zone between the shelf to slope of the southern margin of the Yangtze Platform was stratified, with shallow seawater being oxic but deep water being sulfidic. Subsequently, high denitrification rates prevailed in expanded suboxic areas in spite of a short emergence of an oxic condition in the surface seawater, and the deep seawaters were still anoxic or even euxinic.

Determination of the geographical origin of Chinese teas based on stable carbon and nitrogen isotope ratios

The objective of this study was to investigate the geographical origin of Chinese teas using carbon and nitrogen stable isotope ratio technology.The results showed that inter-provincial dispersion of teas in Guangdong(GD),Guangxi(GX),Hainan(HA),Fujian(FJ),Shandong(SD),Sichuan(SC),Chongqing(CQ),and Henan(HN) provinces was high,while in Zhejiang(ZJ),Hubei(HB),Yunnan(YN),and Anhui(AH) provinces,it was low.Tea samples from GD,GX,HA,and FJ provinces were clustered in one group and separated from those from AH and HB provinces.Thus,carbon and nitrogen stable isotope ratio technology could discriminate teas from among some provinces of China,but not from among others.Better separation might be obtained with a combination of isotopic ratios and other indexes,such as elemental data and organic components.

Nitrogen Isotopes from the Neoproterozoic Liulaobei Formation,North China:Implications for Nitrogen Cycling and Eukaryotic Evolution

The nitrogen isotope compositions(δ^(15)N )of sedimentary rocks can provide information about the nutrient N cycling and redox conditions that may have played important roles in biological evolution in Earth’s history.Although considerableδ^(15)N data for the Precambrian have been published,there is a large gap during the Early Neoproterozoic that restrains our understanding of the linkages among N cycling,ocean redox changes and biological evolution during this key period.Here,we report bulkδ^(15)N and organic carbon isotope(^(δ)13C_(org))compositions as well as the total nitrogen(TN)and total organic carbon(TOC)contents from the Tonian fossiliferous Liulaobei Formation in the southern part of the North China Platform.Theδ^(15)N in the study section is dominated by very stable values centering around+4.3‰,which is moderately lower than that in modern sediments(~+6‰).These positiveδ^(15)N values were attributed to partial denitrification under low primary productivity(scenario 1)and/or denitrification coupled with dissimilatory nitrate reduction to ammonium(DNRA)(scenario 2).In either case,the availability of fixed nitrogen may have provided the nutrient N required to facilitate facilitated eukaryotic growth.Our study highlights the pivotal role of nutrient N in the evolution of eukaryotes.

Spatial distributions of organic carbon and nitrogen and their isotopic compositions in sediments of the Changjiang Estuary and its adjacent sea area

The spatial distribution patterns of total organic carbon and total nitrogen show significant correlations with currents of the East China Sea Shelf. Corresponding to distributions of these currents, the study area could be divided into four different parts. Total organic carbon, total nitrogen, and organic carbon and nitrogen stable isotopes in sediments show linear correlations with mean grain size, respectively, thus ＂grain size effect＂ is an important factor that influences their distributions. C/N ratios can reflect source information of organic matter to a certain degree. In contrast, nitrogen stable isotope shows different spatial distribution patterns with C/N and organic carbon stable isotope, according to their relationships and regional distributions. The highest contribution （up to 50%） of terrestrial organic carbon appears near the Changjiang Estuary with isolines projecting towards northeast, indicating the influence of the Changjiang dilution water. Terrestrial particulate organic matter suffers from effects of diagenesis, benthos and incessant inputting of dead organic matter of plankton, after depositing in seabed. Therefore, the contribution of terrestrial organic carbon to particulate organic matter is obviously greater than that to organic matter in sediments in the same place.

Nitrogen uptake and transfer in broad bean and garlic strip intercropping systems

Utilization and transfer of nitrogen （N）in a strip intercropping system of garlic （Allium safivum L.） and broad bean （Vicia faba L.） have been investigated rarely. The objectives of this study were to quantify N uptake and utilization by intercropped broad bean and garlic and determine the magnitude of N transfer from broad bean to garlic. Field and pot trials were carried out in the Erhai Lake Basin in China using ^15N tracer applied to the soil or injected into broad bean plants. Strip intercropping of garlic and broad bean increased N absorption （47.2%） compared with sole crop broad bean （31.9%） or sole crop garlic （40.7%） and reduced soil residual N. Nearly 15% of 15N injected into petioles of broad bean intercropped with garlic was recovered in garlic at harvest, suggesting that N could be transferred from broad bean to strip intercropped garlic. The findings provide a basis for evaluating legumes＇ role in optimizing N fertilization when intercropped with non-legumes.

Nitrogen Contents and Isotopic Characteristics of Mesozoic and Cenozoic Granites in Northeastern China

The method of determining the nitrogen isotopic composition of granites in the northeastern part of China is described. The content and isotopic values of nitrogen released from granite samples by stepwise heating were determined as well. The results showed that the different areas of northeastern China have a great difference in nitrogen content and isotopic composition. Nitrogen released from the granites is 1.64-6.23μL/g, with the maximum at about 600℃; from rhyolite and granophyre is 108.98-755.96μL/g, with the maximum at about 900℃. It is proved that fluid is characterized by heterogeneity in the deep crust of the different areas in northeastern China. The nitrogen isotopic compositions in different ranges of temperatures are weighted. And the nitrogen isotopic values are +9.2‰ to +17.0‰, with a variation range of 7.8‰. The nitrogen isotopic ratios may have been fractionated during degassing and the fluid released from granites is the residual component.

Analyzing biases of nitrogen contents and δ^(15)N values arising from acidified marine sediments with different CaCO_3 concentrations

In some studies, the researchers pretreated and measured organic carbon, nitrogen and their isotopes（δ^（13）C and δ^（15）N） of marine sediment together, to save costs and resources of analysis. However, the procedure of acidification to remove inorganic carbon for analysing δ^（13）C can affect the values of nitrogen and δ^（15）N, and the biases vary a lot depending on the CaCO_3 contents of sediments. In this study, the biases of total nitrogen（TN）and δ^（15）N values arising from acidified sediments were compared between the CaCO_3-poor（1%–16%） and CaCO_3-rich（20%–40%） samples. TN and δ^（15）N values were altered during acid treatment（without centrifugation） that possibly led to N-containing compounds volatilization. For CaCO_3-poor samples, acidification led to a range of 0%–40% TN losses and 0‰–2‰ shift in δ^（15）N values; and 10%–60% TN losses and 1‰–14‰ shift in δ^（15）N values for CaCO_3-rich samples. The biases from most samples exceeded the precision of the instrument（0.002% for TN and 0.08‰ for δ^（15）N）, and high biases could mislead our judgment for the environmental implication of the data. Thus,avoiding co-analysis of organic carbon, nitrogen and their isotopes（δ^（13）C and δ^（15）N） in sediments, even for CaCO_3-poor marine sediments, is necessary.

Nitrate δ^(15)N and δ^(18)O evidence for active biological transformation in the Changjiang Estuary and the adjacent East China Sea

The Changjiang Estuary has been considered as one of the most polluted estuaries in the world due to high nitrate （NO3） input, especially in spring and summer. In this study, 6~5N and t^180 of NO3, along with other chemical parameters in this area, were measured in spring to evaluate NO3 biogeochemical processes. A simple two end-members mixing model was used to examine the relative contribution of the Changjiang River Diluted Water and marine water to NO~ sources in the Changjiang Estuary and the adjacent East Chi- na Sea. The isotopic signals show that NO3 behaved relatively and conservatively in Transect F and Transect P where assimilation was weak possibly due to vertical mixing, while active assimilation and weak nitrifi- cation occurred in Transect D. Spatial difference in assimilation was indicated by the ~ 1：1 enrichment of S 15N and 6180 in the three transects, while spatial difference in nitrification was reflected by deviations of 15N and 6180 from assimilation line. Our results suggest that the input of the Changjiang River Diluted Wa- ter promoted NO3 assimilation possibly by stratifying the water column which favored the phytoplankton growth.

Tree-ring δ^(15)N of Qinghai spruce in the central Qilian Mountains of China:Is pre-treatment of wood samples necessary?

A knowledge of the tree-ring stable nitrogen isotope ratio(δ^(15)N)can deepen our understanding of forest ecosystem dynamics by indicating the long-term availability,cycling and sources of nitrogen(N).However,the radial mobility of N blurs the interannual variations in the long-term N records.Previous studies of the chemical extraction of tree rings before analysis had produced inconsistent results and it is still unclear whether it is necessary to pre-treat wood samples from specific tree species to remove soluble N compounds before determining theδ^(15)N values.We compared the effects of pre-treatment with organic solvents and hot ultrapure water on the N concentration andδ^(15)N of tree rings from endemic Qinghai spruce(Picea crassifolia)growing in the interior of the central Qilian Mountains,China,during the last 60 a.We assessed the effects of different preparation protocols on the removal of the labile N compounds and investigated the need to pre-treat wood samples before determining theδ^(15)N values of tree rings.Increasing trends of the tree-ring N concentration were consistently observed in both the extracted and unextracted wood samples.The total N removed by extraction with organic solvents was about 17.60%,with a significantly higher amount in the sapwood section(P<0.01).Theδ^(15)N values of tree rings decreased consistently from 1960 to 2019 in both the extracted and unextracted wood samples.Extraction with organic solvents increased theδ^(15)N values markedly by about 5.2‰and reduced the variations in theδ^(15)N series.However,extraction with hot ultrapure water had little effect,with only a slight decrease in theδ^(15)N values of about 0.5‰.Our results showed that the radial pattern in the inter-ring movement of N in Qinghai spruce was not minimized by extraction with either organic solvents or hot ultrapure water.It is unnecessary to conduct hot ultrapure water extraction for the wood samples from Qinghai spruce because of its negligible effect on the removal of the labile N.Theδ^(15)N variation trend of tree rings in the unextracted wood samples was not influenced by the heartwood-sapwood transition zone.We suggest that theδ^(15)N values of the unextracted wood samples of the climate-sensitive Qinghai spruce could be used to explore the ecophysiological dynamics while focusing on the long-term variations.

Evaluation of Accuracy and Precision of IRMS by Using Standard Materials and Applications

The isotope ratio mass spectrometer (IRMS) is an instrument that measures both of the elemental contents and isotope ratios of hydrogen, oxygen, carbon, nitrogen and sulfur in environmental samples at the same time. In this study, we want to try to get two main goals;first, to make up for setting the analytical conditions such as accuracy and precision, second, to apply for comparing of the carbon and nitrogen isotope ratio of sediments in the abandoned mine located in middle province of Korea. For the first goal, a recently introduced IRMS was used to analyze CRM (certified reference materials), which helped to make up the analytical conditions of carbon and nitrogen isotope ratios. So, the accuracy and precision of isotope ratios and elemental contents were also assessed simultaneously, and also the results were very satisfactory. The analytical results of carbon reference materials (EMA-P2) showed an accuracy of -2.801 × 10‰ ± 0.01‰ (2σ) and a precision of 0.009‰ in the mass range from 0.008 μg - 0.162 μg. For nitrogen reference materials (EMA-P2), an accuracy of -1.632‰ ± 0.72‰ (2σ) was obtained in the mass range from 0.082 - 0.162 mg. These values of accuracy and precision are higher than those reported by other studies. For the second goal, carbon and nitrogen isotopes in river sediment near abandoned mines were analyzed based on the established analytical conditions. The result suggested that carbon isotope ratios ranged from -22.5‰ - -7.5‰ and nitrogen isotope ratios from -1.9‰ - 7.9‰. By comparing the isotope ratios and sampling sites of sediment, we know that the nitrogen isotope values in samples of entrance area of mine are greater than those of the farm house area, which is indicating the effects of organic materials. So, we could guess that the newly accumulated organic materials were much more in the farm house area than mine entrance area. And a result of this study, the accuracy and precision tests of IRMS using certified reference materials were very satisfactory and optimum analytical conditions were established well. And also, it was found that the applications of isotopic analysis for environmental samples by using the IRMS could be very useful for the studies on tracing pollution sources.

Origin of the Diamonds within Chromitite from the Mirdita Ophiolite(Albania) and its Geological Significance

Geophysical investigations and laboratory experiments show evidence for possible subduction of ancient oceanic crust.Geological and mineralogical observations suggest that subducted oceanic crust is recycled into the upper mantle.The subduction is supported by the recovery of superdeep diamonds from kimberlites and the presence of crustal materials in ophiolitic chromitites and their host peridotites.What is the mechanism?Here we report the new discovery of ophiolite-hosted diamonds in the podiform chromitites within the Skenderbeu massif from the Mirdita ophiolite in the western part of Neo-Tethys(Fig.1).The diamonds are characterized by exceedingly light C isotopes(δ13CPDB^-25‰),which can be interpreted as evidence for subduction of organic carbon from Earth’s surface.The diamonds are also characterized by an exceptionally large range inδ15Nair(-12.9‰to+25.5‰),accompanied by a low N aggregation state(Fig.2).On the other hand,materials sparsely included in diamonds include amorphous material,Ni-Mn-Co alloy,nanocrystals(20 nm×20 nm)of calcium silicate with an orthorhombic perovskite structure(Ca-Pv),and fluids(Fig.3).We consider that the Skenderbeu diamonds nucleated and grew from a C-saturated,NiMnCo-rich melt derived from a subducted slab of ocean crust and lithosphere in the deep mantle environment.The environment is in the diamond stability field or near the top of the mantle transition zone.The new discovery of diamonds from the Mirdita ophiolite provides a valuable opportunity to understand deep cycling of subducted oceanic crust and mantle(i.e.,composition and process).

Coupled δ^(15)N_(TN) and δ^(13)C_(TOC) Insights into Methane Seepage Activities in Bulk Marine Sediments of the Qiongdongnan Basin, South China Sea

Recently,methane seepage related to the dissociation of natural gas hydrates has attracted much attention,which has a significant impact on the study of the global carbon and nitrogen cycles.Based on the detailed geochemical analyses of sediments(core Q6)from the Qiongdongnan Basin,South China Sea,three methane seepage activities were identified and the exact horizons of anaerobic oxidation of methane(AOM)were defined.Furthermore,organic carbon isotopic(δ^(13)C_(TOC))levels ranged from−23.6‰–−20.6‰PDB;nitrogen isotopes(δ^(15)N_(TN))of the same sedimentary samples ranged from 1.8‰–5.3‰.We also found obvious simultaneous negative excursions of organic carbon isotopes(δ^(13)C_(TOC))and nitrogen isotopes(δ^(15)N_(TN))in the horizons of methane seepages.Compared with the normal sediments,their maximum negative excursions were 2.6‰and 2.5‰,respectively.We discuss in detail the various characteristics ofδ^(15)N_(TN) andδ^(13)C_(TOC) levels in sediments and their coupling responses to methane seepage activities.We believe that the methane seepage events changed the evolution trajectory ofδ^(15)N_(TN) andδ^(13)C_(TOC) levels in sediment records,which resulted in the simultaneous negative excursions.This phenomenon is of great significance to reveal the historical dissociation of natural gas hydrates and their influence on the deep-sea carbon and nitrogen pool.

Influencing factors and significance of organic and inorganic nitrogen isotopic compositions in lacustrine sedimentary rocks

Comprehensive nitrogen biogeochemical cycle has been reconstructed for representative lacustrine organic-rich sedimentary rock in China,namely the Triassic Yanchang Formation(YF,199–230 Ma)in Ordos and the Cretaceous Qingshankou Formation(QF,86–92 Ma)in Songliao basins,by evaluating the organic and inorganic nitrogen isotopic compositions rather than only organic or bulk nitrogen isotopic compositions.The results indicate that the nitrogen isotope values of bulk rock(δ^(15)N_(bulk))in the non-metamorphic stage are significantly different from that of kerogen,which challenge the conceptual framework of sedimentary nitrogen isotope interpretation.Theδ^(15)N_(bulk)from the YF and QF were lower than their respective the nitrogen isotope values of kerogen(δ^(15)N_(ker)),with offsets up to5.1‰,which have the inverse relationship for the metamorphosed rock.Thermal evolution did not significantly modify the d15N of bulk rock and kerogen.The d15N of sediments from the YF(δ^(15)N_(bulk),1.6‰–5.6‰)were lower than that of rock from the QF(δ^(15)N_(bulk),10.2‰–15.3‰).The nitrogen isotope values of silicate incorporated nitrogen(δ^(15)N_(sil))were slightly lower than those of the d15Nker in the YF and obviously lower for the QF.The fact that different nitrogen cycles occur in the YF and QF due to the different depositional redox conditions leads to different isotopic results.The YF water environment dominated by oxic conditions is not conducive to the occurrence of denitrification and anammox,and no abundant N2 loss leads to the relatively lightδ^(15)N_(bulk).In the stratified water for the QF,redox transition zone promotes denitrification and anammox,resulting in the heavyδ^(15)N_(bulk)of rock and promotes the DNRA,resulting in heavyδ^(15)N_(ker)and lowδ^(15)N_(sil).

燃烧源氨排放对灰霾期间北京大气铵的重要贡献

Aerosol ammonium(NH_(4)^(+)),mainly produced from the reactions of ammonia(NH_(3))with acids in the atmosphere,has significant impacts on air pollution,radiative forcing,and human health.Understanding the source and formation mechanism of NH_(4)^(+)can provide scientific insights into air quality improvements.However,the sources of NH_(3)in urban areas are not well understood,and few studies focus on NH_(3)/NH_(4)^(+)at different heights within the atmospheric boundary layer,which hinders a comprehensive understanding of aerosol NH_(4)^(+).In this study,we perform both field observation and modeling studies(the Community Multiscale Air Quality,CMAQ)to investigate regional NH_(3)emission sources and vertically resolved NH_(4)^(+)formation mechanisms during the winter in Beijing.Both stable nitrogen isotope analyses and CMAQ model suggest that combustion-related NH_(3)emissions,including fossil fuel sources,NH_(3)slip,and biomass burning,are important sources of aerosol NH_(4)^(+)with more than 60%contribution occurring on heavily polluted days.In contrast,volatilization-related NH_(3)sources(livestock breeding,N-fertilizer application,and human waste)are dominant on clean days.Combustion-related NH_(3)is mostly local from Beijing,and biomass burning is likely an important NH_(3)source(~15%–20%)that was previously overlooked.More effective control strategies such as the two-product(e.g.,reducing both SO_(2)and NH_(3))control policy should be considered to improve air quality.

Nitrogen pollution and source identification of urban ecosystem surface water in Beijing

Nitrogen contamination of surface water is a worldwide environmental problem with intensive agricul- ture and high population densities. We assessed the spatial and seasonal variation in concentrations of total nitrogen and different nitrogen species present in surface-water in Beijing, China. Also, chemical （NO3-N/C1-） and isotopic （615Nnitrate） indicators were used to identify nitrate sources. The results showed that, during 2009 and 2010, nitrate nitrogen concentrations ranged from 0.7 to 7.6 mg· L^-1, ammonium nitrogen from 0. I to 3.4 mg· L^-1, and total nitrogen from 2.4 to 17.0mg· L^-1. Inorganic nitrogen accounted for between 60 and 100% of total nitrogen at the ten monitoring sites. Nitrate nitrogen, ammonium nitrogen, and total nitrogen concentrations at the 2 downstream monitoring sites in south-eastern Beijing were significantly higher than those at the other eight upstream monitoring sites （P 〈 0.01）. Examination of seasonal variation showed that there was a significant inverse relationship between nitrate nitrogen concentrations and precipitation, and that nitrate nitrogen concentrations peaked in the dry seasons. The information given by the 15Nnitrate values and nitrate nitrogen concentrations, combined with the NO3-N/C1- ratio distribution, showed that domestic sewage was the major source of nitrate in Beijing. Methods to control and reduce sewage pollution are urgently needed to help manage surface water quality in Beijing.

Resorption-related nitrogen changes in the leaves and roots of Larix kaempferi seedlings under nutrient-sufficient and nutrient-starvation conditions

Aims Larch is the dominant timber species in Northeast China.However,compared with the adjacent secondary forests,soil available ni-trogen(N)significantly declined in~40-year-old larch plantations.Thus,it is of great importance to determine how N use strategies in larch change in response to declining soil N availability.Methods We investigated the changes in N concentration and ^(15)N natural abundance(δ^(15)N)from 18 August to 25 October in the leaves,stems,branches and roots of 1-year-old Larix kaempferi seedlings under nutrient-sufficient(NSu)and nutrient-starvation(NSt)condi-tions with a pot experiment in Northeast China.Important Findings Stem and branch N concentrations exhibited upward trends,and leaf N concentration exhibited a downward trend.Root N concentration exhibited an upward trend under NSu conditions,but a downward trend under NSt conditions.These results suggested that stems and branches were served as N storage organs,but roots shifted from storage to resorption organs when switched from NSu to NSt.Leaf nutrient resorption was intensely occurred on 11 October,as indi-cated by the sharply decreased leaf N concentration and increased stem,root and branch N concentrations.Theδ^(15)N of roots,branches and leaves overlapped between NSu and NSt approximately on 11 October,which may be regulated by isotope discrimination dur-ing N resorption.Leaf N resorption efficiency under NSt(76.33%)was significantly higher than that of NSu(56.76%),indicating that nutrient stress stimulates leaf N resorption.Taken together,larch seedlings enhance leaf nutrient resorption and shift roots from nu-trient storage to nutrient resorption to adapt to NSt conditions.These changes might relieve the adverse effects of declining soil nutrient availability on seedling survival and regeneration.

Impacts of silver nanoparticles on enzymatic activities,nitrifying bacteria,and nitrogen transformation in soil amended with ammonium and nitrate

Silver nanoparticles(AgNPs)are effective antimicrobial compounds that are used in a myriad of applications.Soil microorganisms play crucial roles in nitrogen cycling,but there is a lack of comprehensive understanding of the effects of Ag NPs on enzymatic activity in the nitrogen cycle,nitrifying bacteria,and nitrogen transformation in soil.Herein,enzyme activities were determined following the addition of different forms of nitrogen,ammonium nitrogen((NH_(4))_(2)SO_(4)),nitrate nitrogen(KNO_(3)),and amide nitrogen(urea,CO(NH_(2))_(2))at 200 mg N kg^(-1),into the soil amended with AgNPs at 0,10,50,and 100 mg kg^(-1).After 7 d of incubation with 10 mg kg^(-1) Ag NPs,the activities of urease,nitrite reductase(NiR),nitrate reductase(NaR),and hydroxylamine reductase(HyR)were reduced by 12.5%,25.0%,12.2%,and 24.2%,respectively.Of particular note,more than 53.5%,61.7%,and 34.7% of Na R,NiR,and HyR activities,respectively,were inhibited at 100 mg kg^(-1) Ag NPs.The abundance(most probable number)of ammonia-and nitrite-oxidizing bacteria(AOB and NOB,respectively)was measured using real-time quantitative polymerase chain reaction(qPCR)and the Cochran method.The abundance of AOB and NOB decreased when Ag NPs were present in the soil.The NH_(4)NO_(3) amendment increased copy numbers of bacterial and archaeal amo A nitrification functional genes,by 38.3% and 12.4%,respectively,but AgNPs at 50 mg kg^(-1) decreased these values by 70% and 56.4%,respectively.The results of ^(15)N enrichment(atom% excess)of NH_(4)^(+) and NO_(3)^(-) experiments illustrated the influence of AgNPs on soil nitrogen transformation.According to the ^(15)N atom% excess detected,the conversion of ^(15)N-labeled NH_(4)^(+) to NO_(3)^(-) was significantly inhibited by the different levels of Ag NPs in soil.The reduced gross nitrification rate further confirmed this finding.Overall,this study revealed considerable evidence that AgNPs inhibited nitrogen cycle enzyme activity,the number of nitrifying bacteria,the abundance of the amo A gene,and the gross nitrification rate.Silver nanoparticles inhibited nitrogen transformation,and the rate of nitrification was also negatively correlated with AgNP levels.