A stdudy was conducted to determine the seasonal changes of soil respiration and the contribution of root respiration to soil respiration in Betula plaophylla forest in Changbai Mountain from May to September in 2004....A stdudy was conducted to determine the seasonal changes of soil respiration and the contribution of root respiration to soil respiration in Betula plaophylla forest in Changbai Mountain from May to September in 2004. Results indicated that the total soil respiration, root-severed soil respiration and the root respiration followed a similar seasonal trend, with a high rate in summer due to wet and high temperature and a low rate in spring and autumn due to lower temperature. The mean rates of total soil respiration, root-severed soil respiration and root respiration were 4.44, 2.30 and 2.14 μmol.m^-2.s^-1, respectively during the growing season, and they were all exponentially correlated with temperature. Soil respiration rate had a linear correlation with soil volumetric moisture. The Q10 values for total soil respiration, root-severed soil respiration and root respiration were 2,82, 2.59 and 3. 16, respectively. The contribution rate of root respiration to the total soil respiration was between 29.3% and 58.7% during the growing season, indicating that root is a major component of soil respiration. The annual mean rates of total soil respiration, root-severed soil respiration and root respiration were 1.96, 1.08, and 0.87 μmol.m^-2.s^-1, or 741.73 408.71, and 329.24 g.m^-2.a^-1, respectively. Root respiration contributed 44.4% to the annual total soil respiration. The relationship proposed for soil respiration with soil lemperature was useful for understanding and predicting potential changes in Changbai Mountain B. platyphylla forest ecosystem in response to forest management and climate change.展开更多
Wind not only causes extensive damages to trees in many parts of the world, it also has more subtle effects on the growth and morphology of trees and forest ecology as well. Wind damage to trees has historically been ...Wind not only causes extensive damages to trees in many parts of the world, it also has more subtle effects on the growth and morphology of trees and forest ecology as well. Wind damage to trees has historically been the field of silviculture, but increasing recognition of the importance and complexity of the subject has recently got people involved from many other disciplines. Due to the global climate changes, it is believed that the risk of further and stronger storms is increasing. In order to better understand the effects of wind on individual trees, forest stand and forest ecosystem, and further to practice the management of forests, it is necessary to summarize the research results related to this subject. This review was mostly based on the references from recent researches in the field, especially from the symposium volumes of some international conferences on this subject. The results indicated that there have been significant progresses in the following aspects: 1) the aerodynamic interaction between wind and trees, 2) the mechanics of trees under wind loading and adaptive growth, 3) the tree's physiological responses to wind, and 4) the risk assessment of wind damage to forest. However, there are some aspects which may need further studies: 1) wind damage to natural forests, 2) wind-driven gap formation and forest dynamics, 3) the effects of changes resulted from wind disturbances on ecological processes of forest ecosystem, and 4) management for the wind-damaged forests. Key words Wind - Wind effect - Trees/forest - Forest ecology - Disturbance CLC number S718 Document code B Foundation item: This research was supported by “the 100-Young-Researcher Project” of Chinese Academy of Sciences (BR0301) and National Natural Science Foundation (30371149).Biography: ZHU Jiao-jun (1965-), male, Ph. Doctor, Professor of Institute of Applied Ecology, Chinese Academy of Sciences, Professor of Graduate School of Chinese Academy of Sciences. China. Scholar researcher of Faculty of Agriculture, Niigata University, JapanResponsible editor: Song Funan展开更多
The conversion of CO_(2) to methanol with high activity and high selectivity remains challenging owing to the kinetic and thermodynamic limitations associated with the low chemical reactivity exhibited by CO_(2).Herei...The conversion of CO_(2) to methanol with high activity and high selectivity remains challenging owing to the kinetic and thermodynamic limitations associated with the low chemical reactivity exhibited by CO_(2).Herein,we report a novel Cd/TiO_(2) catalyst exhibiting a methanol selectivity of 81%,a CO_(2) conversion of 15.8%,and a CH_(4) selectivity below 0.7%.A combination of experimental and computational studies revealed that the unique electronic properties exhibited by the Cd clusters supported by the TiO_(2) matrix were responsible for the high selectivity of CO_(2) hydrogenation to methanol via the HCOO*pathway at the interfacial catalytic sites.展开更多
CO oxidation is of great importance in both fundamental study and industrial application.Supported noble metal catalysts are highly active for CO oxidation but suffer from the scarcity and high cost.Single-atom cataly...CO oxidation is of great importance in both fundamental study and industrial application.Supported noble metal catalysts are highly active for CO oxidation but suffer from the scarcity and high cost.Single-atom catalysts(SACs)can maximize the metal atom efficiency.Herein,ZnO nanowire(ZnO-nw)supported Rh,Au,and Pt SACs were successfully developed to investigate their CO oxidation performance.Interestingly,it was found that Rh1/ZnO-nw showed much higher activity than the other noble metals which are usually regarded as good candidates for CO oxidation.In addition,the Rh SAC possessed high stability in high-temperature CO oxidation under simulated conditions in the presence of water and hydrocarbons.The high activity and stability make Rh1/ZnO-nw promising for practical applications,especially in the automotive exhaust emission control.Theoretical calculations indicate that the CO oxidation proceeds via the Mars-van Krevelen mechanism and the lowest barrier for the rate-limiting O2 dissociation at a surface oxygen vacancy site is a key factor in determining the observed highest activity of Rh1/ZnO-nw amongst the studied SACs.展开更多
The hydrogenation of CO_(2) into methanol has attracted much attention and In_(2)O_(3) is a promising catalyst.Introducing metal elements into In_(2)O_(3)(M/In_(2)O_(3))is one of the main strategies to improve its per...The hydrogenation of CO_(2) into methanol has attracted much attention and In_(2)O_(3) is a promising catalyst.Introducing metal elements into In_(2)O_(3)(M/In_(2)O_(3))is one of the main strategies to improve its performance.However,its mechanism and active sites remain unclear and need to be further elucidated.Here,the noble‐metal‐free In_(x)‐Co_(y) oxides catalysts were prepared.Much‐improved performance and obvious product selectivity shift were observed.The optimized catalyst(In_(1)‐Co_(4))(9.7 mmol g_(cat)^(–1) h^(–1))showed five times methanol yields than pure In_(2)O_(3)(2.2 mmol g_(cat)^(–1) h^(–1))(P=4.0 MPa,T=300°C,GHSV=24000 cm^(3)_(STP) g_(cat)^(–1) h^(–1),H_(2):CO_(2)=3).And the cobalt‐catalyzed CO_(2) methanation activity was suppressed,although cobalt was most of the metal element.To unravel this selectivity shift,detailed catalysts performance evaluation,together with several in‐situ and ex‐situ characterizations,were employed on cobalt and In‐Co for comparative study.The results indicated CO_(2) hydrogenation on cobalt and In‐Co catalyst both followed the formate pathway,and In‐Co reconstructed and generated a surface In_(2)O_(3)‐enriched core‐shell‐like structure under a reductive atmosphere.The enriched In_(2)O_(3) at the surface significantly enhanced CO_(2) adsorption capacity and well stabilized the intermediates of CO_(2) hydrogenation.CO_(2) and carbon‐containing intermediates adsorbed much stronger on In‐Co than cobalt led to a feasible surface C/H ratio,thus allowing the*CH_(3)O to desorb to produce CH_(3)OH instead of being over‐hydrogenated to CH_(4).展开更多
The design and preparation of suitable supports are of great importance for gold catalysts to attain excellent catalytic performance for alcohol oxidation.In this work,we found that ZnO-CuO mixed oxides supported gold...The design and preparation of suitable supports are of great importance for gold catalysts to attain excellent catalytic performance for alcohol oxidation.In this work,we found that ZnO-CuO mixed oxides supported gold catalysts showed much better catalytic activity for base-free aerobic oxidation of benzyl alcohol than Au/ZnO and Au/CuO catalysts,and among them Au/Zn0.7Cu0.3O displayed the best catalytic performance.In addition,the Au/Zn0.7Cu0.3O catalyst could selectively catalyze the aerobic oxidation of a wide range of alcohols to produce the corresponding carbonyl compounds with high yields under mild conditions without base.Further characterizations indicated that the outstanding catalytic performance of Au/Zn0.7Cu0.3O was correlated with the small size of Au nanoparticles(NPs),good low-temperature reducibility,high concentration of surface oxygen species,and collaborative interaction between Au NPs and mixed oxide.展开更多
Spin engineering is recognized as a promising strategy that modulates the association between d‐orbital electrons and the oxygenated species,and enhances the catalytic kinetics.However,few efforts have been made to c...Spin engineering is recognized as a promising strategy that modulates the association between d‐orbital electrons and the oxygenated species,and enhances the catalytic kinetics.However,few efforts have been made to clarify whether spin engineering could make a considerable enhancement for electrocatalytic water oxidation.Herein,we report the spin engineering of a nanocage‐structured(Co,Ni)Se_(2)/C@FeOOH,that showed significant oxygen evolution reaction(OER)activity.Magnetization measurement presented that the(Co,Ni)Se_(2)/C@FeOOH sample possesses higher polarization spin number(μb=6.966μB/f.u.)compared with that of the(Co,Ni)Se_(2)/C sample(μb=6.398μB/f.u.),for which the enlarged spin polarization number favors the adsorption and desorption energy of the intermediate oxygenated species,as confirmed by surface valance band spectra.Consequently,the(Co,Ni)Se_(2)/C@FeOOH affords remarkable OER product with a low overpotential of 241 mV at a current of 10 mA cm^(-2) and small Tafel slope of 44 mV dec^(-1) in 1.0 mol/L KOH alkaline solution,significantly surpassing the parent(Co,Ni)Se_(2)/C catalyst.This work will trigger a solid step for the design of highly‐efficient OER electrocatalysts.展开更多
基金supported by the Knowledge Inno-vation Project of the Chinese Academy of Sciences (KZCX2-YW-416)the National Natural Science Foundation (90411020)
文摘A stdudy was conducted to determine the seasonal changes of soil respiration and the contribution of root respiration to soil respiration in Betula plaophylla forest in Changbai Mountain from May to September in 2004. Results indicated that the total soil respiration, root-severed soil respiration and the root respiration followed a similar seasonal trend, with a high rate in summer due to wet and high temperature and a low rate in spring and autumn due to lower temperature. The mean rates of total soil respiration, root-severed soil respiration and root respiration were 4.44, 2.30 and 2.14 μmol.m^-2.s^-1, respectively during the growing season, and they were all exponentially correlated with temperature. Soil respiration rate had a linear correlation with soil volumetric moisture. The Q10 values for total soil respiration, root-severed soil respiration and root respiration were 2,82, 2.59 and 3. 16, respectively. The contribution rate of root respiration to the total soil respiration was between 29.3% and 58.7% during the growing season, indicating that root is a major component of soil respiration. The annual mean rates of total soil respiration, root-severed soil respiration and root respiration were 1.96, 1.08, and 0.87 μmol.m^-2.s^-1, or 741.73 408.71, and 329.24 g.m^-2.a^-1, respectively. Root respiration contributed 44.4% to the annual total soil respiration. The relationship proposed for soil respiration with soil lemperature was useful for understanding and predicting potential changes in Changbai Mountain B. platyphylla forest ecosystem in response to forest management and climate change.
基金This research was supported by the 100-Young-Researcher Project of Chinese Academy of Sciences (BR0301) and National Natural Science Foundation (30371149).
文摘Wind not only causes extensive damages to trees in many parts of the world, it also has more subtle effects on the growth and morphology of trees and forest ecology as well. Wind damage to trees has historically been the field of silviculture, but increasing recognition of the importance and complexity of the subject has recently got people involved from many other disciplines. Due to the global climate changes, it is believed that the risk of further and stronger storms is increasing. In order to better understand the effects of wind on individual trees, forest stand and forest ecosystem, and further to practice the management of forests, it is necessary to summarize the research results related to this subject. This review was mostly based on the references from recent researches in the field, especially from the symposium volumes of some international conferences on this subject. The results indicated that there have been significant progresses in the following aspects: 1) the aerodynamic interaction between wind and trees, 2) the mechanics of trees under wind loading and adaptive growth, 3) the tree's physiological responses to wind, and 4) the risk assessment of wind damage to forest. However, there are some aspects which may need further studies: 1) wind damage to natural forests, 2) wind-driven gap formation and forest dynamics, 3) the effects of changes resulted from wind disturbances on ecological processes of forest ecosystem, and 4) management for the wind-damaged forests. Key words Wind - Wind effect - Trees/forest - Forest ecology - Disturbance CLC number S718 Document code B Foundation item: This research was supported by “the 100-Young-Researcher Project” of Chinese Academy of Sciences (BR0301) and National Natural Science Foundation (30371149).Biography: ZHU Jiao-jun (1965-), male, Ph. Doctor, Professor of Institute of Applied Ecology, Chinese Academy of Sciences, Professor of Graduate School of Chinese Academy of Sciences. China. Scholar researcher of Faculty of Agriculture, Niigata University, JapanResponsible editor: Song Funan
文摘The conversion of CO_(2) to methanol with high activity and high selectivity remains challenging owing to the kinetic and thermodynamic limitations associated with the low chemical reactivity exhibited by CO_(2).Herein,we report a novel Cd/TiO_(2) catalyst exhibiting a methanol selectivity of 81%,a CO_(2) conversion of 15.8%,and a CH_(4) selectivity below 0.7%.A combination of experimental and computational studies revealed that the unique electronic properties exhibited by the Cd clusters supported by the TiO_(2) matrix were responsible for the high selectivity of CO_(2) hydrogenation to methanol via the HCOO*pathway at the interfacial catalytic sites.
基金supported by the National Natural Science Foundation of China(21606222,21776270)Liaoning Revitalization Talents Program(XLYC1807068)+1 种基金DNL Cooperation Fund,CAS(180403)US National Science Foundation under CHE-1465057~~
文摘CO oxidation is of great importance in both fundamental study and industrial application.Supported noble metal catalysts are highly active for CO oxidation but suffer from the scarcity and high cost.Single-atom catalysts(SACs)can maximize the metal atom efficiency.Herein,ZnO nanowire(ZnO-nw)supported Rh,Au,and Pt SACs were successfully developed to investigate their CO oxidation performance.Interestingly,it was found that Rh1/ZnO-nw showed much higher activity than the other noble metals which are usually regarded as good candidates for CO oxidation.In addition,the Rh SAC possessed high stability in high-temperature CO oxidation under simulated conditions in the presence of water and hydrocarbons.The high activity and stability make Rh1/ZnO-nw promising for practical applications,especially in the automotive exhaust emission control.Theoretical calculations indicate that the CO oxidation proceeds via the Mars-van Krevelen mechanism and the lowest barrier for the rate-limiting O2 dissociation at a surface oxygen vacancy site is a key factor in determining the observed highest activity of Rh1/ZnO-nw amongst the studied SACs.
文摘The hydrogenation of CO_(2) into methanol has attracted much attention and In_(2)O_(3) is a promising catalyst.Introducing metal elements into In_(2)O_(3)(M/In_(2)O_(3))is one of the main strategies to improve its performance.However,its mechanism and active sites remain unclear and need to be further elucidated.Here,the noble‐metal‐free In_(x)‐Co_(y) oxides catalysts were prepared.Much‐improved performance and obvious product selectivity shift were observed.The optimized catalyst(In_(1)‐Co_(4))(9.7 mmol g_(cat)^(–1) h^(–1))showed five times methanol yields than pure In_(2)O_(3)(2.2 mmol g_(cat)^(–1) h^(–1))(P=4.0 MPa,T=300°C,GHSV=24000 cm^(3)_(STP) g_(cat)^(–1) h^(–1),H_(2):CO_(2)=3).And the cobalt‐catalyzed CO_(2) methanation activity was suppressed,although cobalt was most of the metal element.To unravel this selectivity shift,detailed catalysts performance evaluation,together with several in‐situ and ex‐situ characterizations,were employed on cobalt and In‐Co for comparative study.The results indicated CO_(2) hydrogenation on cobalt and In‐Co catalyst both followed the formate pathway,and In‐Co reconstructed and generated a surface In_(2)O_(3)‐enriched core‐shell‐like structure under a reductive atmosphere.The enriched In_(2)O_(3) at the surface significantly enhanced CO_(2) adsorption capacity and well stabilized the intermediates of CO_(2) hydrogenation.CO_(2) and carbon‐containing intermediates adsorbed much stronger on In‐Co than cobalt led to a feasible surface C/H ratio,thus allowing the*CH_(3)O to desorb to produce CH_(3)OH instead of being over‐hydrogenated to CH_(4).
基金supported by the National Natural Science Foundation of China(21606219)the “Transformational Technologies for Clean Energy and Demonstration”,Strategic Priority Research Program of the Chinese Academy of Sciences(XDA21030900)~~
文摘The design and preparation of suitable supports are of great importance for gold catalysts to attain excellent catalytic performance for alcohol oxidation.In this work,we found that ZnO-CuO mixed oxides supported gold catalysts showed much better catalytic activity for base-free aerobic oxidation of benzyl alcohol than Au/ZnO and Au/CuO catalysts,and among them Au/Zn0.7Cu0.3O displayed the best catalytic performance.In addition,the Au/Zn0.7Cu0.3O catalyst could selectively catalyze the aerobic oxidation of a wide range of alcohols to produce the corresponding carbonyl compounds with high yields under mild conditions without base.Further characterizations indicated that the outstanding catalytic performance of Au/Zn0.7Cu0.3O was correlated with the small size of Au nanoparticles(NPs),good low-temperature reducibility,high concentration of surface oxygen species,and collaborative interaction between Au NPs and mixed oxide.
文摘Spin engineering is recognized as a promising strategy that modulates the association between d‐orbital electrons and the oxygenated species,and enhances the catalytic kinetics.However,few efforts have been made to clarify whether spin engineering could make a considerable enhancement for electrocatalytic water oxidation.Herein,we report the spin engineering of a nanocage‐structured(Co,Ni)Se_(2)/C@FeOOH,that showed significant oxygen evolution reaction(OER)activity.Magnetization measurement presented that the(Co,Ni)Se_(2)/C@FeOOH sample possesses higher polarization spin number(μb=6.966μB/f.u.)compared with that of the(Co,Ni)Se_(2)/C sample(μb=6.398μB/f.u.),for which the enlarged spin polarization number favors the adsorption and desorption energy of the intermediate oxygenated species,as confirmed by surface valance band spectra.Consequently,the(Co,Ni)Se_(2)/C@FeOOH affords remarkable OER product with a low overpotential of 241 mV at a current of 10 mA cm^(-2) and small Tafel slope of 44 mV dec^(-1) in 1.0 mol/L KOH alkaline solution,significantly surpassing the parent(Co,Ni)Se_(2)/C catalyst.This work will trigger a solid step for the design of highly‐efficient OER electrocatalysts.
