Biochar amendment is considered a potential strategy to improve soil fertility and mitigate climate change,yet its specific effects on the fate of fertilizer-derived and native soil nitrogen remain unclear.To elucidat...Biochar amendment is considered a potential strategy to improve soil fertility and mitigate climate change,yet its specific effects on the fate of fertilizer-derived and native soil nitrogen remain unclear.To elucidate the effect of biochar amendment on soil nitrogen(N)transformation and nitrous oxide(N2O)emission,a 56-d soil incubation experiment was conducted using15N isotope tracing to monitor the fate of N.Three treatments were set up:ⅰ)no addition of N or biochar control(CK),ⅱ)addition of15N-labeled ammonium sulfate((NH4)2SO4)(NS),andⅲ)combined addition of15N-labeled(NH4)2SO4and biochar(NS+BC).The15N abundances in soil ammonium(NH4+),nitrate(NO3-),microbial biomass N(MBN),particulate organic N(PON),mineral-associated total N(MTN),and N2O were measured.Compared with NS,endogenous soil N-derived NH4+-N and N2O decreased significantly by 34.4%-67.6% and 18.3%-51.2%,respectively,and exogenous N-derived NH4+-N,MTN,and N2O decreased significantly by 49.6%-81.4%,15.0%-47.0%,and 42.3%-76.5%,respectively,in NS+BC during the first 14 d.Biochar amendment significantly increased endogenous and exogenous soil N retention in MBN by 16.7%-40.1% and over 200 times,respectively,during the first 21 d.The endogenous and exogenous soil N retention in PON increased by12.5%-27.0% and 18.2%-78.5%,respectively,over the whole incubation period.For MTN,the endogenous and exogenous soil N retention increased by 3.9%-6.1% and 24.9%-30.6%,respectively,from days 21 to 56.The contribution of endogenous N to the total N2O emission was>80% across treatments.These results show that biochar amendment can mitigate soil N2O emission and promote inorganic N translocation into MBN,PON,and MTN in soil.展开更多
Different plants exist in preferences for ammonium(NH4+)and nitrate(NO3−)as the dominant N source,reflecting their adaptation to habitat environments.Elucidating plant specific nitrogen preferences and inf...Different plants exist in preferences for ammonium(NH4+)and nitrate(NO3−)as the dominant N source,reflecting their adaptation to habitat environments.Elucidating plant specific nitrogen preferences and influencing factors is crucial for ecosystem management under climate change.In this study,we synthesized 216 observations from15N isotopic tracer studies of diverse forests and grasslands in China to elucidate variations in and factors influencing soil inorganic nitrogen uptake by woody and herbaceous plants.Woody plants had significantly higher uptake rates and proportional contributions of15NH4+than15NO3−(P<0.05),while herbaceous plants exhibited a contrary trend(P<0.05).Mean annual temperature played a significantly role in regulating both15NH4+and15NO3−uptake rates in woody and herbaceous plants,followed by mean annual precipitation,mean annual inorganic nitrogen deposition rates,and soil total nitrogen content(P<0.05).In addition,the key factors influencing nitrogen preference of woody and herbaceous plants were woody plant functional types(evergreen and deciduous plants)and soil inorganic nitrogen content,respectively.Based on the different functional types of woody plants,evergreen plants preferred15NH4+,while deciduous plants preferred15NO3−.The results reveal inorganic nitrogen patterns by different plant types in China and that mean annual temperature is a key determinant of plant nitrogen uptake rates.Thus,by matching species-specific nitrogen preferences with the environmental conditions of different regions,valuable insights can be gained to improve the uptake of inorganic N by different plant types and cope with N limitation.展开更多
Denitrification plays a critical role in mitigating anthropogenic nitrate(NO3-) accumulation in ecosystems.The isotopic composition of NO3-(δ15N and δ18O) serves as a powerful tracer for identifyin...Denitrification plays a critical role in mitigating anthropogenic nitrate(NO3-) accumulation in ecosystems.The isotopic composition of NO3-(δ15N and δ18O) serves as a powerful tracer for identifying N sources and transformation processes.Denitrification often superimposed on the isotope effects of NO2- oxidation, resulting in parallel enrichment of δ15N-and δ18O-NO3-(Δδ18O:Δδ15N trajectory) that causes them to be either below or above 1.This study compared the Δδ18O:Δδ15N trajectory during denitrification, functional genes(nar G, nap A, and nxr A), and carbon sources from metabolites in the Δδ18O:Δδ15N trajectories below or above 1 in unsaturated zones.The results revealed that NO3- reduction was more important for variation in the Δδ18O:Δδ15N trajectory because the difference in isotope effects(15ε_(NO_(3 reduction)) and 18ε_(NO_(3 reduction))) between the two Δδ18O:Δδ15N trajectory groups was significant, whereas the difference in isotope effects(15εnxr and 18εnxr) upon NO2- oxidation was not.Carbon sources in the group with Δδ18O:Δδ15N trajectories below 1 facilitated more efficient electron production to promote NO3- reduction because of their low molecular weight and simple structure.Conversely, the lower electron production efficiency due to the high molecular weight and complex structures of carbon sources in the group with Δδ18O:Δδ15N trajectories above 1 downregulated the expression of the three functional genes(nar G, nap A, and nxr A).The group with Δδ18O:Δδ15N trajectories below 1 showed significantly higher levels of 15ε_(NO_(3 reduction)), 18ε_(NO_(3 reduction)), NO2- oxidation ratio, and copy numbers of nar G, nap A, and nxr A genes compared to the other group, revealing that NO3- reduction at the cellular level was more active in the former group.This study elucidated the integrated infiuence of isotope effects, NO3- reductase and NO2- oxidoreductase activities, and carbon sources from metabolites.These findings are significant for understanding the Δδ18O:Δδ15N trajectories of N cycling in terrestrial ecosystems and support groundwater conservation by improving carbon supplementation approaches that stimulate denitrification, with Δδ18O:Δδ15N trajectories serving as effective tracers for assessing denitrification performance in terrestrial environments.展开更多
The development of organic frameworks with radical skeletons is desired.In this study,we report the development of a novel two-dimensional radical halogen-bonded organic framework(XOF).The radical monomer,benzimidazol...The development of organic frameworks with radical skeletons is desired.In this study,we report the development of a novel two-dimensional radical halogen-bonded organic framework(XOF).The radical monomer,benzimidazole triphenylmethyl(BTTM),was synthesized through the coupling of TTM radicals with benzimidazole.Initially,the benzimidazole units were coordinated with Ag+ions to create a[N···Ag···N]+framework.Subsequently,the addition of iodine led to the in situ replacement of Ag+with I+ions,forming[N···I···N]+linkers and resulting in the creation of the XOF structure.The resulting XOF-HBTTM and XOF-BTTM structures demonstrated good-crystallinity,confirmed by PXRD,HR-TEM,SEAD,and SAXS analyses.EPR measurements confirmed the preservation of radical characteristics within the XOF framework.Furthermore,SQUID measurements indicated that XOF-BTTM exhibits spin moments of S=1/2 at 2 K,with a saturated magnetization strength peaking at 4.10 emu/g,a notable enhancement compared to 1.87 emu/g for the BTTM monomer.This improvement in magnetism is attributed to the extended spin density distribution and the presence of[N···I···N]+interactions,as suggested by DFT calculations.Additionally,the radical XOF-BTTM exhibited significantly enhanced electrical conductivity,reaching up to 1.30×10-4S/cm,which is two orders of magnitude higher than that of XOF-HBTTM.This increased conductivity is linked to a reduced HOMO-LUMO gap,higher carrier density,and the incorporation of triphenylmethyl radicals within the framework.This research highlights the potential of benzimidazolyl motifs in constructing functional XOFs and advances our understanding of radical organic frameworks.展开更多
Nitrogen use efficiency in rice is lower than in upland crops,likely due to differences in soil nitrogen dynamics and crop nitrogen preferences.However,the specific nitrogen dynamics in paddy and upland systems and th...Nitrogen use efficiency in rice is lower than in upland crops,likely due to differences in soil nitrogen dynamics and crop nitrogen preferences.However,the specific nitrogen dynamics in paddy and upland systems and their impact on crop nitrogen uptake remain poorly understood.The N dynamics and impact on crop N uptake determine the downstream environmental pollution from nitrogen fertilizer.To address this poor understanding,we analyzed 2,044 observations of gross nitrogen transformation rates in soils from 136 studies to examine nitrogen dynamics in both systems and their effects on nitrogen uptake in rice and upland crops.Our findings revealed that nitrogen mineralization and autotrophic nitrification rates are lower in paddies than in upland soil,while dissimilatory nitrate reduction to ammonium is higher in paddies,these differences being driven by flooding and lower total nitrogen content in paddies.Rice exhibited higher ammonium uptake,while upland crops had over twice the nitrate uptake.Autotrophic nitrification stimulated by p H reduced rice nitrogen uptake,while heterotrophic nitrification enhanced nitrogen uptake of upland crops.Autotrophic nitrification played a key role in regulating the ammonium-to-nitrate ratio in soils,which further affected the balance of plant nitrogen uptake.These results highlight the need to align soil nitrogen dynamics with crop nitrogen preferences to maximize plant maximize productivity and reduce reactive nitrogen pollution.展开更多
We present new data on the63Cu(γ,n)cross-section studied using a quasi-monochromatic and energy-tunableγbeam produced at the Shanghai Laser Electron Gamma Source to resolve the long-standing discrepancy between e...We present new data on the63Cu(γ,n)cross-section studied using a quasi-monochromatic and energy-tunableγbeam produced at the Shanghai Laser Electron Gamma Source to resolve the long-standing discrepancy between existing measurements and evaluations of this cross-section.Using an unfolding iteration method,63Cu(γ,n)data were obtained with an uncertainty of less than 4%,and the inconsistencies between the available experimental data were discussed.Theγ-ray strength function of63Cu(γ,n)was successfully extracted as an experimental constraint.We further calculated the cross-section of the radiative neutron capture reaction62Cu(n,γ)using the TALYS code.Our calculation method enables the extraction of(n,γ)cross-sections for unstable nuclides.展开更多
Straw return has demonstrated significant potential for enhancing carbon(C)sequestration and nitrogen(N)uptake while concurrently promoting plant productivity.However,the specific transport and distribution of C produ...Straw return has demonstrated significant potential for enhancing carbon(C)sequestration and nitrogen(N)uptake while concurrently promoting plant productivity.However,the specific transport and distribution of C produced by photosynthesis and exogenous N within the rice plant-soil system under straw return remains unclear.A long-term straw return pot trial experiment was conducted in a double cropping rice system,incorporating treatments of inorganic fertilizer application with straw removal(F),straw burning and ash return with reducing inorganic fertilizers(SBR),and straw return with reducing inorganic fertilizers(SR)to investigate C sequestration and exogenous N uptake using 13C pulse and 15N isotope tracer techniques.The SR treatment had significantly higher soil 13C abundance,by 24.4 and 25.4%,respectively,13C concentrations in aboveground plant parts,by 18.4 and 35.8%respectively,and 15N concentrations in rice panicles,by 12.8 and 34.3%than the SBR and F treatments.This enhancement contributed to a higher total organic C concentration and increased rice grain yield in the SR treatment.Furthermore,the SR treatment had significantly higher photosynthetic C,by 9.8%,which was directly transferred to soil C.The SR treatment had a higher distribution of photosynthetic C in the leaves and stems,but a lower distribution in the panicle compared to the SBR treatment.This finding is advantageous for sequestering photosynthetic C into the soil through straw return;conversely,opposite trends were observed in 15N distribution.In addition,rice plants in the SR treatment had increased N uptake from urea and soil N sources,enhancing N recovery by 9.2 and 12.5%,respectively,and reducing soil N residues.Correlation analysis showed that the SR treatment increased the concentrations of 13C in leaves and roots while decreasing the 15N abundance in all rice organs,thereby contributing to an increase in rice yield.The partial least square path model suggested that the increase in rice yield under the SR treatment was primarily linked to 13C accumulation within the rice plant-soil system.The results suggest that straw return increases the sequestration of photosynthetic C and exogenous N in the rice plant-soil system and increases N utilization efficiency,which subsequently improves both rice and soil productivity.展开更多
The neutron capture resonance parameters for 159Tb are crucial for validating nuclear models,nucleosynthesis during the neutron capture process,and nuclear technology applications.In this study,resonance analyses were...The neutron capture resonance parameters for 159Tb are crucial for validating nuclear models,nucleosynthesis during the neutron capture process,and nuclear technology applications.In this study,resonance analyses were performed for the neutron capture cross sections of 159Tb measured at the China Spallation Neutron Source(CSNS)backscattering white neutron beamline(Back-n)facility.The resonance parameters were extracted from the R-Matrix code SAMMY and fitted to the experimental capture yield up to the 1.2 keV resolved resonance region(RRR).The average resonance parameters were determined by performing statistical analysis on the set of the resonance parameters in the RRR.These results were used to fit the measured average capture cross sections using the FITACS code in the unresolved resonance region from 2 keV to 1 MeV.The contributions of partial waves l=0,1,2 to the average capture cross sections are reported.展开更多
This paper extends the previous work[1]for the three-temperature gray radiative transfer equations to the frequency-dependent case.Since the additional frequency variable is considered,the equations are more complicat...This paper extends the previous work[1]for the three-temperature gray radiative transfer equations to the frequency-dependent case.Since the additional frequency variable is considered,the equations are more complicated than those in the gray case.Moreover,opacity may be typically a decreasing function of the frequency variable in applications.At the same spatial location,the equations can be in the optically thick case for low frequency photons,while in the optically thin case for high frequency ones.Thus,the resulting discrete equations can significantly increase the computational cost for opacity having the multi-scale property in multiple frequency radiation.Due to the presence of the radiation-electron coupling,electronion coupling,and electron-ion diffusion terms,the model under consideration exhibits strong nonlinearity and strong coupling properties.In this paper,the multigroup method is used to discretize the frequency variable and the HNTmethod to discretize the angular variable first.Then,within the framework of a unified gas kinetic scheme(UGKS),a multigroup HNT-UGKS method is constructed to solve this complex model iteratively.Furthermore,it can be shown that as the Knudsen number tends to zero,with variations in the electron-ion coupling,absorption,and scattering coefficients,the multigroup HNT-UGKS scheme can converge to numerical schemes for the single-temperature,two-temperature,and the frequency-dependent three-temperature,two-temperature diffusion limit equations,respectively.Finally,several numerical examples are provided to validate the effectiveness and stability of the proposed scheme.展开更多
It remains a significant challenge to explore halogen bonds(XB)based on chlorine,despite extensive investigation into those involving larger halogen atoms like iodine and bromine.The[N…Cl…N]+ halogen bond is usua...It remains a significant challenge to explore halogen bonds(XB)based on chlorine,despite extensive investigation into those involving larger halogen atoms like iodine and bromine.The[N…Cl…N]+ halogen bond is usually unstable and typically only obtainable at extremely low temperatures(approximately−80℃)due to chlorine’s high electronegativity.In this work,we demonstrated the inaugural construction of stable chlorine(Ⅰ)-bridged two-dimensional halogen-bonded organic frameworks(XOFs)utilizing sensitive[N…Cl…N]+ XB.The formation of XOF(Cl)-TPy-BF4/OTf was investigated using proton nuclear magnetic resonance,X-ray photoelectron spectroscopy,infrared,high-resolution transmission electron microscopy,selected area electron diffraction,powder X-ray diffraction,and smallangle X-ray scattering,exhibiting its good crystallinity.Unlike the highly unstable Py2ClBF4/OTf,XOF(Cl)displayed remarkable chemical and thermal stability,even maintaining the periodic framework integrity across various organic solvents.Moreover,the XOF(Cl)can be utilized as a platform to stabilize and immobilize the reactive Pd(0)clusters among the frameworks.The resulting XOF(Cl)-TPy-Pd0 demonstrated excellent catalytic activities in various Pd-catalyzed coupling reactions,including Suzuki,Heck,and Sonogashira couplings,affording high yields even under ambient conditions.Importantly,the synthesis of industrially relevant biphenyl-based liquid crystal molecules using XOF(Cl)-TPy-Pd0 resulted in no detectable palladium residue and the catalyst could be easily recovered via simple filtration and recycled multiple times with consistent catalytic performance.This work not only advances our understanding of chlorine(Ⅰ)chemistry but also establishes a new strategy for the design and development of stable XOFs.The successful demonstration of XOF(Cl)as a robust platform for stabilizing and utilizing reactive species highlights its promising potential for applications in catalysis and beyond.展开更多
基金supported by the Innovation Program of Chinese Academy of Agricultural Sciences(No.CAASCSAL-202302)the Project of Young Innovation Team in the Universities of Shandong Province,China(No.2023KJ218)。
摘要Biochar amendment is considered a potential strategy to improve soil fertility and mitigate climate change,yet its specific effects on the fate of fertilizer-derived and native soil nitrogen remain unclear.To elucidate the effect of biochar amendment on soil nitrogen(N)transformation and nitrous oxide(N2O)emission,a 56-d soil incubation experiment was conducted using15N isotope tracing to monitor the fate of N.Three treatments were set up:ⅰ)no addition of N or biochar control(CK),ⅱ)addition of15N-labeled ammonium sulfate((NH4)2SO4)(NS),andⅲ)combined addition of15N-labeled(NH4)2SO4and biochar(NS+BC).The15N abundances in soil ammonium(NH4+),nitrate(NO3-),microbial biomass N(MBN),particulate organic N(PON),mineral-associated total N(MTN),and N2O were measured.Compared with NS,endogenous soil N-derived NH4+-N and N2O decreased significantly by 34.4%-67.6% and 18.3%-51.2%,respectively,and exogenous N-derived NH4+-N,MTN,and N2O decreased significantly by 49.6%-81.4%,15.0%-47.0%,and 42.3%-76.5%,respectively,in NS+BC during the first 14 d.Biochar amendment significantly increased endogenous and exogenous soil N retention in MBN by 16.7%-40.1% and over 200 times,respectively,during the first 21 d.The endogenous and exogenous soil N retention in PON increased by12.5%-27.0% and 18.2%-78.5%,respectively,over the whole incubation period.For MTN,the endogenous and exogenous soil N retention increased by 3.9%-6.1% and 24.9%-30.6%,respectively,from days 21 to 56.The contribution of endogenous N to the total N2O emission was>80% across treatments.These results show that biochar amendment can mitigate soil N2O emission and promote inorganic N translocation into MBN,PON,and MTN in soil.
基金supported by the Natural Science Basic Research Program of Shaanxi Province(2025JC-YBMS-221)National Natural Science Foundation of China(41977425)College Students Innovation and Entrepreneurship Training Program of Shaanxi Province(S202510712770).
摘要Different plants exist in preferences for ammonium(NH4+)and nitrate(NO3−)as the dominant N source,reflecting their adaptation to habitat environments.Elucidating plant specific nitrogen preferences and influencing factors is crucial for ecosystem management under climate change.In this study,we synthesized 216 observations from15N isotopic tracer studies of diverse forests and grasslands in China to elucidate variations in and factors influencing soil inorganic nitrogen uptake by woody and herbaceous plants.Woody plants had significantly higher uptake rates and proportional contributions of15NH4+than15NO3−(P<0.05),while herbaceous plants exhibited a contrary trend(P<0.05).Mean annual temperature played a significantly role in regulating both15NH4+and15NO3−uptake rates in woody and herbaceous plants,followed by mean annual precipitation,mean annual inorganic nitrogen deposition rates,and soil total nitrogen content(P<0.05).In addition,the key factors influencing nitrogen preference of woody and herbaceous plants were woody plant functional types(evergreen and deciduous plants)and soil inorganic nitrogen content,respectively.Based on the different functional types of woody plants,evergreen plants preferred15NH4+,while deciduous plants preferred15NO3−.The results reveal inorganic nitrogen patterns by different plant types in China and that mean annual temperature is a key determinant of plant nitrogen uptake rates.Thus,by matching species-specific nitrogen preferences with the environmental conditions of different regions,valuable insights can be gained to improve the uptake of inorganic N by different plant types and cope with N limitation.
基金financially supported by the National Natural Science Foundation of China (42361144860, 41973017 and 32071861)。
摘要Denitrification plays a critical role in mitigating anthropogenic nitrate(NO3-) accumulation in ecosystems.The isotopic composition of NO3-(δ15N and δ18O) serves as a powerful tracer for identifying N sources and transformation processes.Denitrification often superimposed on the isotope effects of NO2- oxidation, resulting in parallel enrichment of δ15N-and δ18O-NO3-(Δδ18O:Δδ15N trajectory) that causes them to be either below or above 1.This study compared the Δδ18O:Δδ15N trajectory during denitrification, functional genes(nar G, nap A, and nxr A), and carbon sources from metabolites in the Δδ18O:Δδ15N trajectories below or above 1 in unsaturated zones.The results revealed that NO3- reduction was more important for variation in the Δδ18O:Δδ15N trajectory because the difference in isotope effects(15ε_(NO_(3 reduction)) and 18ε_(NO_(3 reduction))) between the two Δδ18O:Δδ15N trajectory groups was significant, whereas the difference in isotope effects(15εnxr and 18εnxr) upon NO2- oxidation was not.Carbon sources in the group with Δδ18O:Δδ15N trajectories below 1 facilitated more efficient electron production to promote NO3- reduction because of their low molecular weight and simple structure.Conversely, the lower electron production efficiency due to the high molecular weight and complex structures of carbon sources in the group with Δδ18O:Δδ15N trajectories above 1 downregulated the expression of the three functional genes(nar G, nap A, and nxr A).The group with Δδ18O:Δδ15N trajectories below 1 showed significantly higher levels of 15ε_(NO_(3 reduction)), 18ε_(NO_(3 reduction)), NO2- oxidation ratio, and copy numbers of nar G, nap A, and nxr A genes compared to the other group, revealing that NO3- reduction at the cellular level was more active in the former group.This study elucidated the integrated infiuence of isotope effects, NO3- reductase and NO2- oxidoreductase activities, and carbon sources from metabolites.These findings are significant for understanding the Δδ18O:Δδ15N trajectories of N cycling in terrestrial ecosystems and support groundwater conservation by improving carbon supplementation approaches that stimulate denitrification, with Δδ18O:Δδ15N trajectories serving as effective tracers for assessing denitrification performance in terrestrial environments.
基金supported by National Natural Science Foundation of China(Nos.22371218,21702153,52270070 and21801194)Natural Science Foundation of Zhejiang Province(No.LR22B020001)+1 种基金Wuhan Science and Technology Bureau(No.whkxjsj009)the support of the Core Facility of Wuhan University and the Large-scale Instrument and Equipment Sharing Foundation of Wuhan University。
摘要The development of organic frameworks with radical skeletons is desired.In this study,we report the development of a novel two-dimensional radical halogen-bonded organic framework(XOF).The radical monomer,benzimidazole triphenylmethyl(BTTM),was synthesized through the coupling of TTM radicals with benzimidazole.Initially,the benzimidazole units were coordinated with Ag+ions to create a[N···Ag···N]+framework.Subsequently,the addition of iodine led to the in situ replacement of Ag+with I+ions,forming[N···I···N]+linkers and resulting in the creation of the XOF structure.The resulting XOF-HBTTM and XOF-BTTM structures demonstrated good-crystallinity,confirmed by PXRD,HR-TEM,SEAD,and SAXS analyses.EPR measurements confirmed the preservation of radical characteristics within the XOF framework.Furthermore,SQUID measurements indicated that XOF-BTTM exhibits spin moments of S=1/2 at 2 K,with a saturated magnetization strength peaking at 4.10 emu/g,a notable enhancement compared to 1.87 emu/g for the BTTM monomer.This improvement in magnetism is attributed to the extended spin density distribution and the presence of[N···I···N]+interactions,as suggested by DFT calculations.Additionally,the radical XOF-BTTM exhibited significantly enhanced electrical conductivity,reaching up to 1.30×10-4S/cm,which is two orders of magnitude higher than that of XOF-HBTTM.This increased conductivity is linked to a reduced HOMO-LUMO gap,higher carrier density,and the incorporation of triphenylmethyl radicals within the framework.This research highlights the potential of benzimidazolyl motifs in constructing functional XOFs and advances our understanding of radical organic frameworks.
基金funded by the National Key Research and Development Program of China(2024YFD1501602)the National Natural Science Foundation of China(42407437)conducted as part of the Coordinated Research Project D1.50.16,implemented by the Soil and Water Management and Crop Nutrition Section of the Joint FAO/IAEA Division of Nuclear Techniques in Food and Agriculture,Department of Nuclear Sciences and Applications,Vienna,Austria。
摘要Nitrogen use efficiency in rice is lower than in upland crops,likely due to differences in soil nitrogen dynamics and crop nitrogen preferences.However,the specific nitrogen dynamics in paddy and upland systems and their impact on crop nitrogen uptake remain poorly understood.The N dynamics and impact on crop N uptake determine the downstream environmental pollution from nitrogen fertilizer.To address this poor understanding,we analyzed 2,044 observations of gross nitrogen transformation rates in soils from 136 studies to examine nitrogen dynamics in both systems and their effects on nitrogen uptake in rice and upland crops.Our findings revealed that nitrogen mineralization and autotrophic nitrification rates are lower in paddies than in upland soil,while dissimilatory nitrate reduction to ammonium is higher in paddies,these differences being driven by flooding and lower total nitrogen content in paddies.Rice exhibited higher ammonium uptake,while upland crops had over twice the nitrate uptake.Autotrophic nitrification stimulated by p H reduced rice nitrogen uptake,while heterotrophic nitrification enhanced nitrogen uptake of upland crops.Autotrophic nitrification played a key role in regulating the ammonium-to-nitrate ratio in soils,which further affected the balance of plant nitrogen uptake.These results highlight the need to align soil nitrogen dynamics with crop nitrogen preferences to maximize plant maximize productivity and reduce reactive nitrogen pollution.
基金supported by the National Key Research and Development Program(Nos.2023YFA1606901 and 2022YFA1602400)National Natural Science Foundation of China(Nos.U2230133,12275338,and 12388102)Open Fund of the CIAE Key Laboratory of Nuclear Data(No.JCKY2022201C152).
摘要We present new data on the63Cu(γ,n)cross-section studied using a quasi-monochromatic and energy-tunableγbeam produced at the Shanghai Laser Electron Gamma Source to resolve the long-standing discrepancy between existing measurements and evaluations of this cross-section.Using an unfolding iteration method,63Cu(γ,n)data were obtained with an uncertainty of less than 4%,and the inconsistencies between the available experimental data were discussed.Theγ-ray strength function of63Cu(γ,n)was successfully extracted as an experimental constraint.We further calculated the cross-section of the radiative neutron capture reaction62Cu(n,γ)using the TALYS code.Our calculation method enables the extraction of(n,γ)cross-sections for unstable nuclides.
基金supported by the National Natural Science Foundation of China(32160503)the Earmarked Fund for Jiangxi Agriculture Research System,China(JXARS-01)the National Key R&D Program of China(2023YFD2301303).
摘要Straw return has demonstrated significant potential for enhancing carbon(C)sequestration and nitrogen(N)uptake while concurrently promoting plant productivity.However,the specific transport and distribution of C produced by photosynthesis and exogenous N within the rice plant-soil system under straw return remains unclear.A long-term straw return pot trial experiment was conducted in a double cropping rice system,incorporating treatments of inorganic fertilizer application with straw removal(F),straw burning and ash return with reducing inorganic fertilizers(SBR),and straw return with reducing inorganic fertilizers(SR)to investigate C sequestration and exogenous N uptake using 13C pulse and 15N isotope tracer techniques.The SR treatment had significantly higher soil 13C abundance,by 24.4 and 25.4%,respectively,13C concentrations in aboveground plant parts,by 18.4 and 35.8%respectively,and 15N concentrations in rice panicles,by 12.8 and 34.3%than the SBR and F treatments.This enhancement contributed to a higher total organic C concentration and increased rice grain yield in the SR treatment.Furthermore,the SR treatment had significantly higher photosynthetic C,by 9.8%,which was directly transferred to soil C.The SR treatment had a higher distribution of photosynthetic C in the leaves and stems,but a lower distribution in the panicle compared to the SBR treatment.This finding is advantageous for sequestering photosynthetic C into the soil through straw return;conversely,opposite trends were observed in 15N distribution.In addition,rice plants in the SR treatment had increased N uptake from urea and soil N sources,enhancing N recovery by 9.2 and 12.5%,respectively,and reducing soil N residues.Correlation analysis showed that the SR treatment increased the concentrations of 13C in leaves and roots while decreasing the 15N abundance in all rice organs,thereby contributing to an increase in rice yield.The partial least square path model suggested that the increase in rice yield under the SR treatment was primarily linked to 13C accumulation within the rice plant-soil system.The results suggest that straw return increases the sequestration of photosynthetic C and exogenous N in the rice plant-soil system and increases N utilization efficiency,which subsequently improves both rice and soil productivity.
基金supported by the National Natural Science Foundation of China(Nos.12365018,U2032146,12465024)Natural Science Foundation of Inner Mongolia(Nos.2023MS01005,2024ZD23,2024FX30)the program of Innovative Research Team and Young Talents of Science and Technology in Universities of Inner Mongolia Autonomous Region(Nos.NMGIRT2217,NJYT23109)。
摘要The neutron capture resonance parameters for 159Tb are crucial for validating nuclear models,nucleosynthesis during the neutron capture process,and nuclear technology applications.In this study,resonance analyses were performed for the neutron capture cross sections of 159Tb measured at the China Spallation Neutron Source(CSNS)backscattering white neutron beamline(Back-n)facility.The resonance parameters were extracted from the R-Matrix code SAMMY and fitted to the experimental capture yield up to the 1.2 keV resolved resonance region(RRR).The average resonance parameters were determined by performing statistical analysis on the set of the resonance parameters in the RRR.These results were used to fit the measured average capture cross sections using the FITACS code in the unresolved resonance region from 2 keV to 1 MeV.The contributions of partial waves l=0,1,2 to the average capture cross sections are reported.
基金supported by the Beijing Natural Science Foundation(Z230003)for Sunby the National Key R&D Program(2020YFA0712200)+1 种基金the National Key Project(GJXM92579)the Sino-German Science Center(GZ 1465)for Jiang。
摘要This paper extends the previous work[1]for the three-temperature gray radiative transfer equations to the frequency-dependent case.Since the additional frequency variable is considered,the equations are more complicated than those in the gray case.Moreover,opacity may be typically a decreasing function of the frequency variable in applications.At the same spatial location,the equations can be in the optically thick case for low frequency photons,while in the optically thin case for high frequency ones.Thus,the resulting discrete equations can significantly increase the computational cost for opacity having the multi-scale property in multiple frequency radiation.Due to the presence of the radiation-electron coupling,electronion coupling,and electron-ion diffusion terms,the model under consideration exhibits strong nonlinearity and strong coupling properties.In this paper,the multigroup method is used to discretize the frequency variable and the HNTmethod to discretize the angular variable first.Then,within the framework of a unified gas kinetic scheme(UGKS),a multigroup HNT-UGKS method is constructed to solve this complex model iteratively.Furthermore,it can be shown that as the Knudsen number tends to zero,with variations in the electron-ion coupling,absorption,and scattering coefficients,the multigroup HNT-UGKS scheme can converge to numerical schemes for the single-temperature,two-temperature,and the frequency-dependent three-temperature,two-temperature diffusion limit equations,respectively.Finally,several numerical examples are provided to validate the effectiveness and stability of the proposed scheme.
基金support of the Core Facility of Wuhan University and the Large-scale Instrument and Equipment Sharing Foundation of Wuhan University。
摘要It remains a significant challenge to explore halogen bonds(XB)based on chlorine,despite extensive investigation into those involving larger halogen atoms like iodine and bromine.The[N…Cl…N]+ halogen bond is usually unstable and typically only obtainable at extremely low temperatures(approximately−80℃)due to chlorine’s high electronegativity.In this work,we demonstrated the inaugural construction of stable chlorine(Ⅰ)-bridged two-dimensional halogen-bonded organic frameworks(XOFs)utilizing sensitive[N…Cl…N]+ XB.The formation of XOF(Cl)-TPy-BF4/OTf was investigated using proton nuclear magnetic resonance,X-ray photoelectron spectroscopy,infrared,high-resolution transmission electron microscopy,selected area electron diffraction,powder X-ray diffraction,and smallangle X-ray scattering,exhibiting its good crystallinity.Unlike the highly unstable Py2ClBF4/OTf,XOF(Cl)displayed remarkable chemical and thermal stability,even maintaining the periodic framework integrity across various organic solvents.Moreover,the XOF(Cl)can be utilized as a platform to stabilize and immobilize the reactive Pd(0)clusters among the frameworks.The resulting XOF(Cl)-TPy-Pd0 demonstrated excellent catalytic activities in various Pd-catalyzed coupling reactions,including Suzuki,Heck,and Sonogashira couplings,affording high yields even under ambient conditions.Importantly,the synthesis of industrially relevant biphenyl-based liquid crystal molecules using XOF(Cl)-TPy-Pd0 resulted in no detectable palladium residue and the catalyst could be easily recovered via simple filtration and recycled multiple times with consistent catalytic performance.This work not only advances our understanding of chlorine(Ⅰ)chemistry but also establishes a new strategy for the design and development of stable XOFs.The successful demonstration of XOF(Cl)as a robust platform for stabilizing and utilizing reactive species highlights its promising potential for applications in catalysis and beyond.