Temporal and spatial variations of carbon isotope signature reveal substantial contribution of bracts and internode assimilates to grain filling of japonica rice

Carbon isotope composition(δ^(13)C)of a plant organ is an inherent signature reflecting its physiological property,and thus is used as an integrative index in crop breeding.It is also a non-intrusive method for quantifying the relative contribution of different source organs to grain filling in cereals.Using the samples collected from two-year field and pot experiments with two nitrogen(N)fertilization treatments,we investigated the temporal and spatial variations of δ^(13)C in source organs of leaf,sheath,internode,and bracts,and in sink organ grain.Constitutive nature of δ^(13)C was uncovered,with an order of leaf(−27.84‰)<grain(−27.82‰)<sheath(−27.24‰)<bracts(−26.81‰)<internode(−25.67‰).For different positions of individual organs within the plant,δ^(13)C of the leaf and sheath presented a diminishing trend from the top(flag leaf and its sheath)to the bottom(the last leaf in reverse order and its sheath).No obvious pattern was found for the internode.For temporal variations, δ^(13)C of the leaf and sheath had a peak(the most negative)at 10 days after anthesis(DAA),whereas that of the bracts showed a marked increase at the time point of anthesis,implying a transformation from sink to source organ.By comparing the δ^(13)C in its natural abundance in the water-soluble fractions of the sheath,internode,and bracts with the δ^(13)C in mature grains,the relative contribution of these organs to grain filling was assessed.With reference to the leaf,the internode accounted for as high as 32.64%and 42.56%at 10 DAA and 20 DAA,respectively.Meanwhile,bracts presented a larger contribution than the internode,with superior bracts being higher than inferior bracts.In addition,N topdressing reduced the contribution of the internode and bracts.Our findings clearly proved the actual significance of non-foliar organs of the internode and bracts for rice yield formation,thus extending our basic knowledge of source and sink relations.

Differential response of radial growth and δ^(13)C in Qinghai spruce(Picea crassifolia) to climate change on the southern and northern slopes of the Qilian Mountains in Northwest China

Tree radial growth can have significantly differ-ent responses to climate change depending on the environ-ment.To elucidate the effects of climate on radial growth and stable carbon isotope(δ^(13)C)fractionation of Qing-hai spruce(Picea crassifolia),a widely distributed native conifer in northwestern China in different environments,we developed chronologies for tree-ring widths and δ^(13)C in trees on the southern and northern slopes of the Qilian Mountains,and analysed the relationship between these tree-ring variables and major climatic factors.Tree-ring widths were strongly influenced by climatic factors early in the growing season,and the radial growth in trees on the northern slopes was more sensitive to climate than in trees on the southern.Tree-ring δ^(13)C was more sensitive to climate than radial growth.δ^(13)C fractionation was mainly influenced by summer temperature and precipitation early in the growing season.Stomatal conductance more strongly limited stable carbon isotope fractionation in tree rings than photosynthetic rate did.The response between tree rings and climate in mountains gradually weakened as climate warmed.Changes in radial growth and stable carbon isotope fractionation of P.crassifolia in response to climate in the Qilian Mountains may be further complicated by continued climate change.

Hydrogeochemical and isotopic assessment of the origin of NO_(3)^(−)and N-NH_(3)contents in the aquifer located in a closed lacustrine volcano-sedimentary basin in the metropolitan area of Mexico City

To explain the presence and spatial distribution of NO_(3)^(−)and N-NH_(3)in the Aquifer of the Metropolitan Area of Mexico City(AMAMC),a hydrogeochemical and isotopic analysis using^(13)C DIC(as well as the stable isotopes^(18)O and^(2)H)in groundwater was conducted.This aquifer is located in an old closed lacustrine volcano-sedimentary basin;some wells hosted in the semi-confined zone contain high N-NH_(3)concentrations,while others present NO_(3)^(−)contents in the recharge zones(hosted in an oxidizing environment).In this study,a change in the isotopic signature(primarily in^(18)O and^(2)H)was observed from the recharge zones to the basin center in some of the wells with high NO_(3)^(−)concentrations,this behavior can be attributed to evaporation during the incorporation of recently infiltrated water.In addition,the results for^(13)C(along with ^(2) H)in wells with the highest N-NH_(3)concentrations exhibited an atypically broad range of values.Results indicated the occurrence of hydrogeochemical and/or biochemical processes in the aquifer(in an oxidizing or reducing environment),such as organic degradation,bacterial decomposition(primarily in the ancient Lake Texcoco and which acts as a natural sink for carbon,nitrogen,sulfur,and phosphorus),besides rock weathering and dissolution,which may be responsible for a very marked isotopic modification of the^(13)C(and,to a lesser extent,2 H).Methanotrophic bacterial activity and methanogenic activity may be related to N-NH_(3)removal processes by oxidation and residual water incorporation respectively,whereas the increase in the NO_(3)^(−)content in some wells is due to the recent contribution of poor-quality water due to contamination.

Pyrolysis mechanism of glucose and mannose: The formation of 5-hydroxymethyl furfural and furfural

Fast pyrolysis of biomass will produce various furan derivatives, among which 5-hydroxymethyl furfural（5-HMF） and furfural（FF） are usually the two most important compounds derived from holocellulose. In this study, density functional theory（DFT） calculations are utilized to reveal the formation mechanisms and pathways of 5-HMF and FF from two hexose units of holocellulose, i.e., glucose and mannose. In addition, fast pyrolysis experiments of glucose and mannose are conducted to substantiate the computational results, and the orientation of 5-HMF and FF is determined by 13C-labeled glucoses. Experimental results indicate that C1 provides the aldehyde group in both 5-HMF and FF, and FF is mainly derived from C1 to C5 segment. According to the computational results, glucose and mannose have similar reaction pathways to form 5-HMF and FF with d-fructose（DF） and 3-deoxy-glucosone（3-DG） as the key intermediates. 5-HMF and FF are formed via competing pathways. The formation of 5-HMF is more competitive than that of FF, leading to higher yield of 5-HMF than FF from both hexoses. In addition, compared with glucose,mannose can form 5-HMF and FF via extra pathways because of the epimerization at C2 position. Therefore, mannose pyrolysis results in higher yields of 5-HMF and FF than glucose pyrolysis.

Trace element geochemistry and stable isotopic(δ^(13)C andδ^(15)N)records of the Paleocene coals,Salt Range,Punjab,Pakistan

The Paleocene coals of the Salt Range in the Punjab Province of Pakistan have great economic potential;however,their trace element and stable isotopic characteristics have not been studied in detail except for a few sporadic samples.In this study,a total of 59 coal samples of which 14 are obtained from open cast mines have been investigated for elemental composition andδ^(13)C-δ^(15)N isotopic signatures.Average contents of trace elements such as Co,Cr,Cu,Pb,Sr,Th,U,V,and Zn are 7.4,41.7,11.2,12.5,90.2,4.0,1.9,128,and 31.1 mg/kg,respectively.These values,when compared with the World Coal Clarke values,were relatively higher in low-rank coals in comparison with Clarke values for brown coals.Likewise,As(20.4 mg/kg),Co(6.6 mg/kg),Cr(22.4 mg/kg),Cu(^(13).3 mg/kg),Pb(19.2 mg/kg),Sr(^(15)4.7 mg/kg),Th(2.5 mg/kg),V(47.8 mg/kg),and Zn(75.1 mg/kg)were significantly higher in the sub-bituminous to bituminous coals of the Salt Range.Mineralogical analysis,based on X-ray diffraction and energy dispersive X-ray spectroscopy,revealed that the studied samples contain illite,kaolinite calcite,gypsum,pyrite,and quartz.Elemental affinity with organic and inorganic phases of coals calculated by an indirect statistical approach indicated a positive association of ash content with Ag,Al,Co,Cr,Cs,Cu,Mn,P,Rb,Pb,Th,U,and V,suggesting the presence of inorganic components in studied coals.However,As,Fe,Sr,and Zn exhibit negative correlations that imply their association with the organic fraction.Theδ^(13)C andδ^(15)N isotopic range and average−24.94‰to−25.86‰(−25.41‰)and−2.77‰to 3.22‰(0.96‰),respectively,reflecting 3C type modern terrestrial vegetation were common in the palaeomires of studied coal seams.In addition,the trivial variations of 0.92‰and 0.45‰among^(13)C and^(15)N values can be attributed to water level fluctuations and plant assemblies.

Use of δ^(18)O, δ^(13)C and NO_(3)^(-) to identify hydrogeochemical processes related to contamination in an aquifer located in central Mexico

In this work,an isotopic analysis of δ^(18)O,δ^(13)C,and NO_(3)^(-) concentrations was carried out to identify the origin and the processes related to the contamination of an aquifer located in the state of Guanajuato,Mexico.The research identified the possible sources of δ^(13)C in groundwater.During groundwater flow,CO_(2) participates in different hydrogeochemical reactions in which the dissolution of carbonates or biochemical processes related to biodegradation stand out.Isotopic data of δ^(13)C,δ^(18)O,and the hydrogeochemical behavior of NO_(3)^(-) and HCO_(3)^(-) in water,in addition to isotopic data and the chemical composition of limestones in the study area,were determined to establish the isotopic signature and the processes undergone by the rocks.The isotopic signature of rock and water samples indicated that metamorphic limestones contributed with carbon dioxide to deep groundwater,while in the upper aquifer,bacterial metabolic reactions during nitrification–denitrification could modify the isotopic signature of δ^(13)C in some wells,although atmospheric contribution also plays a role.The modification of the carbon isotopic component is related to the precipitation of calcite in specific regions of the study area,input of atmospheric CO_(2),and soil(e.g.the possible participation of C4-type plants in the assimilation-release of carbon).This process is not confirmed or completely ruled out in this study since agriculture is excessively developed throughout the region.The joint interpretation of isotopic values and the hydrogeochemical behavior of major and conservative elements help in identifying possible pollution processes in which different carbon sources are related.

Sedimentary Organic Matter Characterization on a Tropical Continental Shelf in Northeastern Brazil

In continental shelf areas works where the focus is Geochemistry are widely relevant, due to the vast complexity and uses of these relief features (social, environmental and economic). On the Brazilian Northeast tropical shelves, with emphasis on the Pernambuco Continental Shelf (PCS), the published studies are limited and have aimed at portions closer to the coastline. The objective of the present work is the description of the characteristics and origin of sedimentary organic matter (SOM) in the inner and middle Pernambuco shelf, defining and classifying the local geochemical sedimentary facies. The sampling stations (136) were collected in the study area, and the grain-size, contents of total organic matter (TOM), calcium carbonate (CaCO3) were analyzed. The samples were processed in an elemental analyzer coupled with a mass spectrometer after the elimination of calcium carbonate. The obtained data were the grain-size, TOM, CaCO3, elemental (C, N) and the stable isotopic ratios of δ13C e δ15N of SOM. Based on the measured values of carbon and nitrogen, the C/N ratio, associated to δ13C e δ15N, is observed that in the PCS predominates an organic matter of marine origin along its entire length: C < 1%, N < 1%, C/N < 5, δ13C > -21 PDB e δ15N > 8Ar. The PCS presents patches of continental origin SOM, associated to the coastal zones adjacent to estuarine systems mouths and covering the paleochannels, which may indicate that this material was carried from the coastal rivers to the offshore areas, possibly by the paleo-valleys that also act as traps of fine sediments and SOM. The statistical analysis indicates the existence of 6 different sedimentary facies and a prevalence of one of them, characterized by poorly-sorted bioclastic sandy-gravel, with low to medium organic contents of marine origin. This indicates that the coastal sedimentary material contributions are low and the local cover is autochthonous of biogenic origin, and deposited according to the surficial topography, morphosedimentary processes and meteoceanographycal conditionings of the study area, typical of moderate hydrodynamic energy environments.

Power-law patterns in the Phanerozoic sedimentary records of carbon, oxygen, sulfur,and strontium isotopes

Power-law patterns appear in a variety of natural systems on the modern Earth;nevertheless,whether such behaviors appeared in the deep-time environment has rarely been studied. Isotopic records in sedimentary rocks, which are widely used to reconstruct the geological/geochemical conditions in paleoenvironments and the evolutionary trajectories of biogeochemical cycles, offer an opportunity to investigate power laws in ancient geological systems. In this study, I focus on the Phanerozoic sedimentary records of carbon, oxygen, sulfur, and strontium isotopes, which have well documented and extraordinarily comprehensive datasets. I perform statistical analyses on these datasets and show that the variations in the sedimentary records of the four isotopes exhibit power-law behaviors. The exponents of these power laws range between 2.2 and 2.9;this narrow interval indicates that the variations in carbon, oxygen, sulfur, and strontium isotopes likely belong to the same universality class, suggesting that these systematic power-law patterns are governed by universal, scale-free mechanisms. I then derive a general form for these power laws from a minimalistic model based on basic physical principles and geosystem-specific assumptions, which provides an interpretation for the power-law patterns from the perspective of thermodynamics. The fundamental mechanisms regulating such patterns might have been ubiquitous in paleoenvironments, implying that similar power-law behaviors may exist in the sedimentary records of other isotopes.

A quantum cascade laser infrared spectrometer for CO_2 stable isotope analysis：Field implementation at a hydrocarbon contaminated site under bio-remediation

Real-time methods to monitor stable isotope ratios of CO_2 are needed to identify biogeochemical origins of CO_2 emissions from the soil–air interface. An isotope ratio infra-red spectrometer（IRIS） has been developed to measure CO_2 mixing ratio with δ~13C isotopic signature, in addition to mixing ratios of other greenhouse gases（CH_4, N2_O）. The original aspects of the instrument as well as its precision and accuracy for the determination of the isotopic signature δ~13C of CO_2 are discussed. A first application to biodegradation of hydrocarbons is presented, tested on a hydrocarbon contaminated site under aerobic bio-treatment. CO_2 flux measurements using closed chamber method is combined with the determination of the isotopic signature δ~13C of the CO_2 emission to propose a non-intrusive method to monitor in situ biodegradation of hydrocarbons. In the contaminated area, high CO_2 emissions have been measured with an isotopic signature δ~13C suggesting that CO_2 comes from petroleum hydrocarbon biodegradation.This first field implementation shows that rapid and accurate measurement of isotopic signature of CO_2 emissions is particularly useful in assessing the contribution of contaminant degradation to the measured CO_2 efflux and is promising as a monitoring tool for aerobic bio-treatment.

Effects of nitrogen addition on carbonate-derived CO_(2) emission after biochar addition

●We studied the effect of nitrogen and biochar on CO_(2) emission from SOC and SIC.●Nitrogen increased SIC-derived CO_(2) by 41%but decreased SOC-derived CO_(2) by 20%.●Biochar reduced total soil-derived CO_(2) by neutralizing nitrogen-induced acidity.●We proposed a method for 3-or 4-source partitioning CO_(2) emission from calcareous soils.Biochar addition generally increases the alkalinity regeneration to resist soil acidification driven by nitrogen(N)fertilization.Calcareous soils contain soil organic carbon(SOC)and inorganic C(SIC).Owing to technical limitations in three-source partitioning CO_(2),how biochar addition affects SOC-and SIC-derived CO_(2) emission has not been clarified yet.Therefore,we conducted a 70-day incubation experiment of ammonium-N and maize-straw-derived biochar additions to investigate the N plus biochar impacts on SOC-and SIC-derived CO_(2) emission.Over the 70-day incubation,we found that the N-only addition increased the SIC-derived CO_(2) emission by approximately 41%compared with the control,but decreased the SOC-derived CO_(2) emission by approximately 20%.This suggests that the distinct responses of SIC-and SOC-derived CO_(2) emission to N-only addition come from N-induced acidification and preferential substrate(N)utilization of soil microorganisms,respectively.Compared with N-only addition,N plus biochar addition decreased the SIC-derived CO_(2) emission by 17%−20%during the first 20 days of incubation,but increased it by 54%during the next 50 days.This result suggested that biochar addition reduced the SIC-derived CO_(2) emission likely due to the alkalization capacity of biochar exceeding the acidification capacity of ammonium-N in the short term,but it may increase the SIC-derived CO_(2) emission induced by the weak acidity produced from biochar mineralization in the long term.This study is helpful to improve the quantification of CO_(2) emission from calcareous soils.

Combined application of biochar with fertilizer promotes nitrogen uptake in maize by increasing nitrogen retention in soil

Combined application of biochar with fertilizers has been used to increase soil fertility and crop yield.However,the coupling mechanisms through which biochar improves crop yield at field scale and the time span over which biochar affects carbon and nitrogen transformation and crop yield are still little known.In this study,a long-term field trial(2013-2019)was performed in brown soil planting maize.Six treatments were designed:CK-control;NPK-application of chemical fertilizers;C1PK-low biochar without nitrogen fertilizer;C1NPK,C_(2)NPK and C_(3)NPK-biochar at 1.5,3 and 6 t ha^(−1),respectively,combined with chemical fertilizers.Results showed that theδ^(15)N value in the topsoil of 0-20 cm layer in the C_(3)NPK treat-ment reached a peak of 291‰at the third year(2018),and demonstrated a peak of 402‰in the NPK treatment in the initial isotope trial in 2016.Synchronously,SOC was not affected until the third to fourth year after biochar addition,and resulted in a significant increase in total N of 2.4 kg N ha^(−1) in 2019 in C_(3)NPK treatment.During the entire experiment,the ^(15)N recovery rates of 74-80%were observed highest in the C_(2)NPK and C_(3)NPK treatments,resulting in an annual increase in yields significantly.The lowest subsoilδ^(15)N values ranged from 66‰to 107‰,and the ^(15)N residual rate would take 70 years for a complete decay to 0.001%in the C_(3)NPK.Our findings suggest that biochar compound fertilizers can increase C stability and N retention in soil and improve N uptake by maize,while the loss of N was minimized.Biochars,therefore,may have an important potential for improving the agroecosystem and ecological balance.

Influencing factors and partitioning methods of carbonate contribution to CO_(2)emissions from calcareous soils

In calcareous soils,recent studies have shown that soil-derived CO_(2)originates from both soil organic carbon(SOC)decomposition and soil inorganic carbon(SIC)dissolution,a fact often ignored in earlier studies.This may lead to overestimation of the CO_(2)emissions from SOC decomposition.In calcareous soils,there is a chemical balance between precipitation and dissolution of CaCO_(3)-CO_(2)-HCO_(3),which is affected by soil environmental factors(moisture,temperature,pH and depth),root growth(rhizosphere effect)and agricultural measures(organic materials input,nitrogen fertilization and straw removal).In this paper,we first introduced the contribution of SIC dissolution to CO_(2)emissions from calcareous soils and their driving factors.Second,we reviewed the methods to distinguish two CO_(2)sources released from calcareous soils and quantify the 13C fractionation coefficient between SIC and SIC-derived CO_(2)and between SOC and SOC-derived CO_(2),and to partition three CO_(2)sources released from soils with plants and organic materials input.Finally,we proposed methods for accurately distinguishing three CO_(2)sources released from calcareous soils.This review helps to improve the accuracy of soil C balance assessment in calcareous soils,and also proposes the direction of further investigations on SIC-derived CO_(2)emissions responses to abiotic factors and agricultural measures.

Lake geochemistry reveals marked environmental change in Southwest China during the Mid Miocene Climatic Optimum

The Mid-Miocene Climatic Optimum （MMCO; 15-17 Ma） was one of the short-term climatic warm events that punctuated the Cenozoic long-term cooling trend. Because there are very few terrestrial records of this event, most of our understanding comes from marine cores. In this report, we first present new palaeomagnetic data that revises the dating of our 400 m-thick lacustrine section in Wenshan （Yunnan）, previously thought to be Late Mio- cene. These new data suggest an older age, ca. 15.2-16.5 Ma, coinciding with the MMCO. We measured δ13C on bulk organic matter （3 Corg）, total organic carbon （TOC）, total nitrogen （TN） and C/N ratios at a high sample resolution to： （1） reconstruct the palaeoenvironmental changes in the lake catchment area, and （2） infer mechanisms responsible for these changes. Our results show that all four geochemical parameters demonstrate that a strong environmental change occurred around the middle of the section, shortly after the C5Cn/C5Br geomagnetic reversal and the Early/Middle Miocene boundary at 15.97 Ma. We propose that the environmental shift may be due to a combination of a change in climate, which became cooler, together with a change in organic matter cycling within the lake. This study provides a new insight into the MMCO and demonstrates that although the MMCO was generally a warm event, it was also a time of climatic instability and abrupt environmental changes.

Aquatic Species Dominate Organic Matter in Qinghai Lake during the Holocene:Evidence from Eolian Deposits around the Lake

Total organic carbon（TOC） in lake sediments and its stable carbon isotope（δ（13）C（org）） are widely applied to investigate paleoenvironmental changes even though their implications are complicated and multi-explanatory. Organic geochemistry studies of lake sediments from Qinghai Lake have been investigated, but some interpretations are controversial. In this study, TOC of one Holocene eolian section and δ（13）C（org） of three eolian sections were studied around Qinghai Lake. Results indicate that the TOC content in eolian deposits was low during the Early Holocene, and gradually increased to high values during the Middle and Late Holocene. The variation in TOC content of eolian deposits is different from that in the lacustrine sequence from Qinghai Lake during the Holocene. The δ（13）C（org） values in the eolian sections were relatively stable, with oscillation amplitudes of 4‰（ranging from-25.8‰ to-22.1‰）, in contrast to 10‰ variation s in δ（13）C（org） values（varying from-30‰ to-20‰） in lacustrine sediments. Through comparison of TOC and δ（13）C（org） values between eolian deposits and lacustrine sediments, we can confirm indications that the organic matter in Qinghai Lake sediments during the Holocene was primarily a contribution of the aquatic species in the lake. This is significant for understanding the origin of organic matter in lake sediments on the northeastern Qinghai-Tibetan Plateau and for paleoenvironmental inferences using such proxies.

The precipitation “threshold value” on C_4/C_3 abundance of the Loess Plateau, China

In this paper, we report organic carbon isotopic characterizations from two loess sequences （JY and GL）, spanning the last 20 ka, from the northwest Chinese Loess Plateau （CLP）. The results indicate that the vegetation type is nearly pure C3 plants in the studied region during the Holocene. In contrast to other reported loess sequences in the central-southeast CLP, the relative abundance of the C4 plants decreases from southeast to northwest, with the vegetation types changing from pure C3 to a C4/C3 mixture should near 36°N in the Holocene. From the perspective of the modem temperature and precipitation distribution, the summer temperature has no obvious change at the same latitude, but there are differences in the summer precipi- tation, which exhibit an obvious increase from west to east. Further analysis indicated that the C4 plant abundance decreases with the decreasing summer season precipitation from the southeast to the northwest CLP during the Holocene. We suggest that with the absence of favorable precipitation condition, increasing temperature and decreasing atmospheric CO2 concentration are insufficient to drive an expansion of the C4 plants on the CLP in the Holocene. According to a Holocene precipitation recon- struction, a ＂threshold value＂ of summer precipitation existed, which mainly controlled the expansion of C4 plants. Compared with the modern δ13Csom and climate data on the CLP, both the Holocene and the present ＂threshold value＂ are near the 360-mm summer precipitation line, although the present precipitation line turned slightly southwestward. Our results provide new insights for further research on the C4/C3 variations with precipi- tation and the relationship to global C4/C3 change.

Biochar application significantly increases soil organic carbon under conservation tillage:an 11-year field experiment

Biochar application and conservation tillage are significant for long-term organic carbon(OC)sequestration in soil and enhancing crop yields,however,their effects on native soil organic carbon(native SOC)without biochar carbon sequestration in situ remain largely unknown.Here,an 11-year field experiment was carried out to examine different biochar application rates(0,30,60,and 90 Mg ha^(−1))on native SOC pools(native labile SOC pool I and II,and native recalcitrant SOC)and microbial activities in calcareous soil across an entire winter wheat-maize rotation.The proportions of C_(3) and C_(4)-derived native SOC mineralization were quantified using soil basal respiration(SBR)combined with 13C natural isotope abundance measurements.The results showed that 39-51%of the biochar remained in the top 30 cm after 11 years.Biochar application rates significantly increased native SOC and native recalcitrant SOC contents but decreased the proportion of native labile SOC[native labile SOC pool I and II,dissolved organic carbon(DOC),and microbial biomass carbon(MBC)].Biochar application tended to increase the indicators of microbial activities associated with SOC degradation,such as SBR,fluorescein diacetate hydrolysis activity,and metabolic quotient(qCO_(2)).Meanwhile,higher biochar application rates(B60 and B90)significantly increased the C_(4)-derived CO_(2) proportion of the SBR and enhanced C_(4)-derived native SOC mineralization.The effect of the biochar application rate on the content and proportion of native SOC fractions occurred in the 0-15 cm layer,however,there were no significant differences at 15-30 cm.Soil depth also significantly increased native labile SOC pool Ⅰ and Ⅱ contents and decreased qCO_(2).In conclusion,the biochar application rate significantly increased native SOC accumulation in calcareous soil by enhancing the proportion of native recalcitrant SOC,and biochar application and soil depth collectively influenced the seasonal turnover of native SOC fractions,which has important implications for long-term agricultural soil organic carbon sequestration.