The Kop ophiolite in NE Turkey is a fragment of Neo-Tethyan forearc.It can be mainly divided into a paleo-Moho transition zone(MTZ)in the North and a harzburgitic mantle sequence in the South.Dunites are predominant i...The Kop ophiolite in NE Turkey is a fragment of Neo-Tethyan forearc.It can be mainly divided into a paleo-Moho transition zone(MTZ)in the North and a harzburgitic mantle sequence in the South.Dunites are predominant in the MTZ of the Kop ophiolite,and they are locally interlayered with chromitites and enclose minor bodies of harzburgites near the petrological Moho boundary.Large Fe isotopic variations were observed for magnesiochromite(-0.14‰to 0.06‰)and olivine(-0.12‰to 0.14‰)from the MTZ chromitites,dunites and harzburgites.In individual dunite samples,magnesiochromite usually has lighter Fe isotopic compositions than olivine,which was probably caused by subsolidus Mg-Fe exchange between the two mineral phases.Both magnesiochromite and olivine display an increasing trend ofδ56Fe along a profile from chromitite todunite.This trend reflects continuous fractional crystallization in a magma chamber,which resulted in heavier Fe isotopes concentrated in the evolved magmas.In each cumulative cycle of chromitite and dunite,dunite was formed from relatively evolved melts after massive precipitation of magnesiochromite.Mixing of more primitive and evolved melts in the magma chamber was a potential mechanism for triggering the crystallization of magnesiochromite,generating chromitite layers in the cumulate pile.Before mixing happened,the primitive melts had reacted with mantle harzburgites during their ascendance;whereas the evolved melts may lie on the olivine-chromite cotectic near the liquidus field of pyroxene.Variable degrees of magma mixing and differentiation are expected to generate melts with differentδ56Fe values,accounting for the Fe isotopic variations of the Kop MTZ.展开更多
The effects of ammonium (NH4+-N) and nitrate (NO3- - N) were examined on Fe fractions and FeCN (ferricyanide) reductase activity in intact root tips (0-3 cm) of young maize (Zea mays L. cv. Lenz) in solution culture b...The effects of ammonium (NH4+-N) and nitrate (NO3- - N) were examined on Fe fractions and FeCN (ferricyanide) reductase activity in intact root tips (0-3 cm) of young maize (Zea mays L. cv. Lenz) in solution culture by using short-term experiment under controlled Fe deficiency conditions (containing high HCO3- concentration in pre-culture solution). The results showed that Fe(Ⅱ) concentrations in root tip apoplast of maize were only 20-40 nmol/g FW which accounted for 7%-13% of total Fe. Most of Fe in root tips existed as Fe(Ⅲ) compounds. Imposition of the roots to NH4+ - N or NO3- - N for 60 min led to an increase of Fe(Ⅱ) in root tip apoplast. NH4+ - N led to an increased concentration of Fe(Ⅱ) and exchangeable Fe (Fe(Ⅱ) and Fe (Ⅲ)) in root tips, while NO3- - N increased FeCN reductase activity. The relationship between pH and Fe fractions, FeCN reductase activity was also discussed.展开更多
Effects of free iron oxyhydrates （Fed） and soil organic matter （SOM） on copper （Cu^2＋） sorption-desorption behavior by size fractions of aggregates from two typical paddy soils （Ferric-Accumulic Stagnic Anthro...Effects of free iron oxyhydrates （Fed） and soil organic matter （SOM） on copper （Cu^2＋） sorption-desorption behavior by size fractions of aggregates from two typical paddy soils （Ferric-Accumulic Stagnic Anthrosol （Soil H） and Gleyic Stagnic Anthrosol （Soil W）） were investigated with and without treatments of dithionite-citrate-bicarbonate and of H2O2. The size fractions of aggregates were obtained from the undisturbed bulk topsoil using a low energy ultrasonic dispersion procedure. Experiments of equilibrium sorption and subsequent desorption were conducted at soil water ratio of 1：20, 25℃. For Soil H, Cu^2＋ sorption capacity of the DCB-treated size fractions was decreased by 5.9% for fine sand fraction, by 40.4% for coarse sand fraction, in comparison to 2.9% for the bnlk sample. However, Cu^2＋ sorption capacities of the H2O2-treated fractions were decreased by over 80% for the coarse sand fraction and by 15% for the clay-sized fraction in comparison to 88% for bulk soil. For Soil W, Cu^2＋ sorption capacity of the DCB-treated size fraction was decreased by 30% for the coarse sand fraction and by over 75% for silt sand fraction in comparison to 44.5% for the bulk sample. Cu^2＋ sorption capacities of the H2O2-treated fractions were decreased by only 2.0% for the coarse sand fraction and by 15% for the fine sand fraction in comparison to by 3.4% for bulk soil. However, Cu^2＋ desorption rates were increased much in H2O2-treated samples by over 80% except the clay-sized fraction （only 9.5%） for Soil H. While removal of SOM with H2O2 tendend to increase the desorption rate, DCB- and H2O2-treatments caused decrease in Cu^2＋ retention capacity of size fractions, Particularly, there hardly remained Cu^2＋ retention capacity by size fractions from Soil H after H2O2 treatment except for clay-sized fraction. These findings supported again the dominance of the coarse sand fraction in sorption of metals and the preference of absorbed metals bound to SOM in differently stabilized status among the size fractions. Thus, enrichment and turnover of SOM in paddy soils may have great effects on metal retention and chemical mobility in paddy soils.展开更多
Ningwu porphyrite-type iron deposits are located in Ningwu Mesozoic volcanic basin,which belongs to the middle and lower reaches of the Yangtze River metallogenic province.The volcanic rocks can be divided into Longwa...Ningwu porphyrite-type iron deposits are located in Ningwu Mesozoic volcanic basin,which belongs to the middle and lower reaches of the Yangtze River metallogenic province.The volcanic rocks can be divided into Longwangshan,Dawangshan,Gushan and Niangniangshan Formations from early to late.All these volcanic rocks are rich in alkali,and show the similar patterns in rare earth element(REE) distribution.However,some differences can be found in the trace elements and REE patterns.The study of petrology and REE geochemical characteristics shows that these rocks are derived from the underplating of the lithospheric mantle and are contaminated by crustal materials,undergo AFC process during the magmatic evolution.展开更多
文摘The Kop ophiolite in NE Turkey is a fragment of Neo-Tethyan forearc.It can be mainly divided into a paleo-Moho transition zone(MTZ)in the North and a harzburgitic mantle sequence in the South.Dunites are predominant in the MTZ of the Kop ophiolite,and they are locally interlayered with chromitites and enclose minor bodies of harzburgites near the petrological Moho boundary.Large Fe isotopic variations were observed for magnesiochromite(-0.14‰to 0.06‰)and olivine(-0.12‰to 0.14‰)from the MTZ chromitites,dunites and harzburgites.In individual dunite samples,magnesiochromite usually has lighter Fe isotopic compositions than olivine,which was probably caused by subsolidus Mg-Fe exchange between the two mineral phases.Both magnesiochromite and olivine display an increasing trend ofδ56Fe along a profile from chromitite todunite.This trend reflects continuous fractional crystallization in a magma chamber,which resulted in heavier Fe isotopes concentrated in the evolved magmas.In each cumulative cycle of chromitite and dunite,dunite was formed from relatively evolved melts after massive precipitation of magnesiochromite.Mixing of more primitive and evolved melts in the magma chamber was a potential mechanism for triggering the crystallization of magnesiochromite,generating chromitite layers in the cumulate pile.Before mixing happened,the primitive melts had reacted with mantle harzburgites during their ascendance;whereas the evolved melts may lie on the olivine-chromite cotectic near the liquidus field of pyroxene.Variable degrees of magma mixing and differentiation are expected to generate melts with differentδ56Fe values,accounting for the Fe isotopic variations of the Kop MTZ.
基金This work was supported by the National Natural Science Foundation of China (Grant Nos. 30000103 and 39870480)the National Key Basic Research Special Funds (Grant No. G1999011707)by the Deutsche Forschungsgemeinschaft (DFG) for a personal grant on th
文摘The effects of ammonium (NH4+-N) and nitrate (NO3- - N) were examined on Fe fractions and FeCN (ferricyanide) reductase activity in intact root tips (0-3 cm) of young maize (Zea mays L. cv. Lenz) in solution culture by using short-term experiment under controlled Fe deficiency conditions (containing high HCO3- concentration in pre-culture solution). The results showed that Fe(Ⅱ) concentrations in root tip apoplast of maize were only 20-40 nmol/g FW which accounted for 7%-13% of total Fe. Most of Fe in root tips existed as Fe(Ⅲ) compounds. Imposition of the roots to NH4+ - N or NO3- - N for 60 min led to an increase of Fe(Ⅱ) in root tip apoplast. NH4+ - N led to an increased concentration of Fe(Ⅱ) and exchangeable Fe (Fe(Ⅱ) and Fe (Ⅲ)) in root tips, while NO3- - N increased FeCN reductase activity. The relationship between pH and Fe fractions, FeCN reductase activity was also discussed.
基金supported by the National Natural Science Foundation of China (No. 40231016).
文摘Effects of free iron oxyhydrates （Fed） and soil organic matter （SOM） on copper （Cu^2＋） sorption-desorption behavior by size fractions of aggregates from two typical paddy soils （Ferric-Accumulic Stagnic Anthrosol （Soil H） and Gleyic Stagnic Anthrosol （Soil W）） were investigated with and without treatments of dithionite-citrate-bicarbonate and of H2O2. The size fractions of aggregates were obtained from the undisturbed bulk topsoil using a low energy ultrasonic dispersion procedure. Experiments of equilibrium sorption and subsequent desorption were conducted at soil water ratio of 1：20, 25℃. For Soil H, Cu^2＋ sorption capacity of the DCB-treated size fractions was decreased by 5.9% for fine sand fraction, by 40.4% for coarse sand fraction, in comparison to 2.9% for the bnlk sample. However, Cu^2＋ sorption capacities of the H2O2-treated fractions were decreased by over 80% for the coarse sand fraction and by 15% for the clay-sized fraction in comparison to 88% for bulk soil. For Soil W, Cu^2＋ sorption capacity of the DCB-treated size fraction was decreased by 30% for the coarse sand fraction and by over 75% for silt sand fraction in comparison to 44.5% for the bulk sample. Cu^2＋ sorption capacities of the H2O2-treated fractions were decreased by only 2.0% for the coarse sand fraction and by 15% for the fine sand fraction in comparison to by 3.4% for bulk soil. However, Cu^2＋ desorption rates were increased much in H2O2-treated samples by over 80% except the clay-sized fraction （only 9.5%） for Soil H. While removal of SOM with H2O2 tendend to increase the desorption rate, DCB- and H2O2-treatments caused decrease in Cu^2＋ retention capacity of size fractions, Particularly, there hardly remained Cu^2＋ retention capacity by size fractions from Soil H after H2O2 treatment except for clay-sized fraction. These findings supported again the dominance of the coarse sand fraction in sorption of metals and the preference of absorbed metals bound to SOM in differently stabilized status among the size fractions. Thus, enrichment and turnover of SOM in paddy soils may have great effects on metal retention and chemical mobility in paddy soils.
基金Project(2011BAB04D01) supported by the National Science and Technology Support Program of China
文摘Ningwu porphyrite-type iron deposits are located in Ningwu Mesozoic volcanic basin,which belongs to the middle and lower reaches of the Yangtze River metallogenic province.The volcanic rocks can be divided into Longwangshan,Dawangshan,Gushan and Niangniangshan Formations from early to late.All these volcanic rocks are rich in alkali,and show the similar patterns in rare earth element(REE) distribution.However,some differences can be found in the trace elements and REE patterns.The study of petrology and REE geochemical characteristics shows that these rocks are derived from the underplating of the lithospheric mantle and are contaminated by crustal materials,undergo AFC process during the magmatic evolution.
