温度对土壤吸附有机肥中可溶性有机碳、氮的影响

可溶性有机碳、氮(Soluble organic carbon or nitrogen,SOC和SON)可被土壤吸附.土壤可溶性有机碳、氮组分复杂,土壤对可溶性有机物吸附的不均一性会导致可溶性有机物组分的变化,大部分疏水性化合物被吸附,而亲水性化合物被释放进入溶液中[1].因此,可溶性有机碳、氮在土壤中的吸附,直接影响其在土壤-水系统中的迁移和行为[2-3].林地土壤中含有相当数量的可溶性有机养分,因此,关于林地土壤对可溶性有机养分的吸附特性,国外研究者已开展了不少研究.研究表明,可溶性有机碳吸附特性与土壤性质如pH、表面积、有机碳、铁铝氧化物和黏粒含量等因素有关[4-5].关于农业土壤对可溶性有机碳的吸附特性的影响,国内也开展了一些研究,主要集中在pH、铁铝氧化物含量等对吸附影响方面[6-9].     

蔬菜连作对铜尾矿土壤中有机碳、腐殖质碳以及可溶性有机碳的影响

Carbon of humus acids （HSAC） and dissolved organic carbon （DOC） are the most active forms of soil organic carbon （SOC） and play an important role in global carbon recycling. We investigated the concentrations of HSAC, water-soluble organic carbon （WSOC）, hot water-extractable organic carbon （HWOC） and SOC in soils under different vegetation types of four copper mine tailings sites with differing vegetation succession time periods in Tongling, China. The concentrations of HSAC, WSOC, HWOC and SOC increased with vegetation succession. WSOC concentration increased with the accumulation of SOC in the tailings, and a linearly positive correlation existed between the concentrations of HSAC and SOC in the tailings. However, the percentages of HSAC and DOC in the SOC decreased during vegetation succession. The rate of SOC accumulation was higher when the succession time was longer than 20 years, whereas the speeds of soil organic matter （SOM） decomposition and humification were slow, and the concentrations of HSAC and DOC increased slowly in the tailings. The percentage of carbon of humic acid （HAC） in HSAC increased with vegetation succession, and the values of humification index （HI）, HAC/carbon of fulvic acid, also increased with the accumulation of HSAC and SOC in soils of the tailings sites. However, the HI value in the each of the tailings was less than 0.50. The humification rate of SOM was lower than the accumulation rate of SOM, and the level of soil fertility was still very low in the tailings even after 40 years of natural restoration.     

离子强度、Cd2+和pH对生物碳吸附西玛津的影响

本研究考察了离子强度、重金属(Cd₂ )和pH对200 °C和400 °C下制备的玉米秸秆生物碳(分别记作CS200和CS400)吸附西玛津的影响。结果表明,炭化程度较高的CS400对西玛津的吸附能力(log K_oc)高于炭化程度较低的CS200,因为CS400具有较强的疏水性、较多的芳香碳且较大的比表面积。尽管H-键作用可能会发生,但是CS400的主导吸附机制为疏水作用、电荷转移(π-π*)作用和孔填充作用,而CS200的主导吸附机制为分配作用。两种生物碳对西玛津的吸附几乎未因离子强度增大和Cd₂ 的存在而受到影响,表明西玛津和生物碳之间未发生离子交换和Cd₂ 并没有起到键桥离子的作用。低的pH有利于两种生物碳对西玛津的吸附。负载西玛津后,CS400的zeta电位显著降低证实了电荷转移(π-π*)的重要作用,而CS200的zeta电位降低不明显说明分配作用为主导。Cd₂ 的存在几乎未改变两种生物碳吸附西玛津的zeta电位表明特定位点的表面吸附并不是生物碳吸附Cd₂ 的主导机制。离子交换可能是生物碳吸附Cd₂ 的主导机制,这也很好解释了CS200比CS400吸附更多的Cd₂ 和Cd₂ 的存在对两种生物碳吸附西玛津几乎未产生影响的原因。     

恒电荷土壤胶体对Cu2+ 、Pb2+ 的静电吸附与专性吸附特征

供试土壤胶体对Cu2 、Pb2 的吸附强度用pH50 值表示 ,其大小次序为 :土 >黄绵土、黑垆土 >黄褐土。离子强度实验和表面络合反应机制证明恒电荷土壤胶体对Cu2 、Pb2 的吸附含有专性吸附 ,n值可作为判断专性吸附与静电吸附比例的特征值 ,低pH值时 ,以水解 -络合吸附为主 ;高pH值时 ,以水解 -络合与沉淀吸附为主。静电吸附和专性吸附的比例与pH有关 ,各土壤胶体专性吸附百分数大小为 :黄褐土 >土 >黑垆土 >黄绵土。不同土壤胶体在同一介质中对Cu2 、Pb2 的固有络合常数logKintM 值及固有络合ΔG m 负值大小次序与吸附强度大小一致。在定pH定浓条件下 ,考虑离子之间的相互作用时 ,土壤胶体对重金属离子的吸附过程可用BDM等温式描述。供试土壤胶体对Cu2 、Pb2 专性吸附ΔG m 的大小与固有络合ΔG m 接近且大小次序也一致。     

用悬液Wien效应研究Na+、K+、NH4+、Ca2+、Zn2+和Cd2+阳离子与红壤黏粒间的相互作用及能量关系

采用悬液Wien效应法研究了Na+、K+、NH4+、Ca2+、Zn2+和Cd2+阳离子与红壤黏粒间的相互作用及能量关系。结果表明,在试验条件下,红壤黏粒与阳离子Na+、K+、NH4+、Ca2+、Zn2+和Cd2+的平均结合自由能分别为:4.50、7.35、7.15、9.12、9.84和9.63 kJ mol-1。含Ca2+悬液的电导率随场强增加而递增最快,含Na+和NH4+悬液的电导率随场强增加而增加最慢,而含K+、Zn2+和Cd2+的悬液电导率的增速相近、介于其间。红壤悬液中不同阳离子的解离速率顺序为Ca2+>K+>Zn2+=Cd2+>Na+=NH4+。在低场强(15～80 kV cm-1)下,不同阳离子的平均吸附自由能ΔGad没有差异。在场强100 kV cm-1以上,二价阳离子的ΔGad明显大于单价阳离子,不同阳离子间ΔGad的大小顺序为NH4+≤Na+>K+=NH4+>Ca2+>Zn2+=Cd2+,Na+离子平均解离度的递增速率(场强增加1kV cm-1所引起的解离度增量)最大,为0.000 427 cm kV-1,其次是Ca2+离子,为0.000 221 cm kV-1,其余阳离子为0.000 12～0.000 14 cm kV-1。     

长期外源有机物料添加对川中丘陵区农田土壤养分和有机碳组分的影响

有机肥和秸秆等有机物料添加是调控土壤肥力的重要手段，可促进农田土壤有机碳的数量和质量发生变化。研究选取盐亭紫色土农业生态试验站长期（16a）6种不同施肥处理试验小区，探究两种形式的外源有机物料（猪粪堆肥和秸秆还田）添加对土壤有机碳及总氮、总磷、硝态氮和速效磷养分含量的影响，并基于固态13C核磁共振波谱技术(13C-NMR)分析其对土壤有机碳化学组分的影响。研究发现，添加有机物料可显著增加0~30 cm土壤有机碳和各养分含量；猪粪堆肥施用对土壤总磷、速效磷和硝态氮含量的影响大于秸秆还田。结果还表明两种有机物料添加改变了耕层土壤有机碳化学组成及其稳定性，有机物料添加增加了0~10 cm表层土壤有机碳中烷氧基碳和羧基碳的比例，降低了烷基碳的比例，同时降低了10~20 cm土层羧基碳比例，增加了烷基碳比例。本研究可为区域旱耕地有机碳库稳定性及其碳汇功能评估提供科学依据。     

NaCl对辽河口湿地土壤溶解性有机碳吸附解吸的影响

以辽河口芦苇湿地0~40 cm深度土壤作为研究对象,采用平衡吸附法,研究了辽河口湿地土壤对不同浓度溶解性有机碳(DOC)的吸附解吸特征,并分析了不同深度土壤以及NaCl处理对DOC吸附解吸的影响。结果表明:辽河口湿地0~10 cm和10~20 cm深度土壤DOC吸附量随DOC浓度增大而下降;20~30 cm和30~40 cm深度土壤DOC吸附量随DOC浓度增大而上升。NaCl处理中,不同深度土壤DOC的可吸附量分别为0.038、0.044、0.021和0.011 g kg-1。除30~40 cm深度土壤外,DOC吸附量显著高于对照处理,且随DOC浓度的升高而增大,明显促进了辽河口湿地土壤对DOC的吸附。NaCl处理对辽河口湿地0~10 cm和10~20 cm深度土壤DOC的解吸量影响不显著,而对20~30 cm、30~40 cm深度土壤DOC的解吸量起到明显促进作用。     

有机酸对针铁矿和膨润土吸附Cd2+、Pb2+的影响

用平衡吸附法研究了不同浓度的有机酸（乙酸、酒石酸和柠檬酸）对针铁矿和膨润土吸附Cd^2＋、Pb^2＋的影响。结果表明：（1）低浓度（〈0．6mmolL^-1）有机酸促进供试矿物吸附Cd^2＋和Pb^2＋，随着有机酸浓度增加，吸附逐渐被抑制。高浓度（〉1．0mmolL^-1）有机酸对Pb^2＋吸附的抑制作用比对Cd^2＋的强。有机酸浓度的变化对针铁矿Cd^2＋、Pb^2＋吸附率的影响大于对膨润土的。（2）不同Cd^2＋浓度下，有机酸对膨润土Cd^2＋吸附强度的影响大于针铁矿。加入高浓度Cd^2＋（8．0mmolL^-1）时，低浓度有机酸对膨润土吸附Cd^2＋的促进作用比加入低浓度Cd^2＋（0．4mmolL^-1）时明显，高浓度有机酸对膨润土吸附Cd^2＋的抑制作用与低浓度Cd^2＋时相近。（3）低浓度有机酸（〈0．6mmolL^-1）时，酒石酸、柠檬酸对针铁矿吸附Cd^2＋的促进作用大于乙酸，而它们对膨润土吸附Cd^2＋的促进作用相似；在三种有机酸高浓度（〉1．0mmol L^-1）时，针铁矿对Cd^2＋的吸附都趋于稳定，而柠檬酸对膨润土吸附Cd^2＋的抑制作用比乙酸和酒石酸的明显。不同种类有机酸下，矿物对Pb^2＋吸附率大小的变化基本一致。     

耕作方式对稻田土壤活性有机碳组分、有机碳矿化以及腐殖质特征的影响

以连续种植三季的稻田土壤为材料,采用大田试验的方法,研究了四种耕作方式(常耕CT、稻草还田常耕SCT、免耕NT、稻草还田免耕SNT)下稻田土壤的活性有机碳组分含量、有机碳矿化以及腐殖质特征。结果表明:在0~5cm土层,免耕(NT、SNT)和稻草还田(SCT、SNT)都能提高土壤中不同活度有机碳以及总有机碳、腐殖酸、胡敏酸的△log K以及E4/E6值,其中以SNT增加效果最为明显,而稻草还田(SCT、SNT)还能提高了土壤有机碳的日矿化量和矿化累积量;在5~20 cm土层,除中活性有机碳外,常耕耕作(CT、SCT)提高了不同活度有机碳、总有机碳、有机碳矿化累积量、腐殖酸、胡敏酸、富里酸、腐殖化度以及胡/富比,其中以SCT的作用最为明显。在短期时间内,免耕结合稻草还田,有利于表层土壤的腐殖化,增加稻田土壤中碳的固定;常耕结合稻草还田更利于5~20cm土层腐殖质的更新与活化,增加土壤中碳的固定,从而减缓新增碳对温室气体的增温效应。     

土壤磷酸盐的吸收对Cu2+二次吸附动力学的影响

The effects of sorbed phosphate on the kinetics of Cu^2 secondary adsorption on three major types of soils in southern and Central China were studied using the batch method and flow (or miscible displacement) techniques.Both of the methods showed that diffusions were the ratedetermining steps in the Cu^2 adsorption by the soils.By the flow method,the course of Cu^2 adsorption kinetics consisted of two steps-sn initial rapid process and a later slow process of Cu^2 adsorption;while by the batch method,the 90% of Cu^2 adsorption reaction was found to finish within first 1 minute.The results obtained using the flow method also indicated that for red soil and yellow-brown soil ,Cu^2 adsorptions during the initial reaction periods were restrained when the soils sorbed phosphate,whereas the adsorption reactions were stimulated at the final time,For grey Chao soil,sorbed phosphate retarded the Cu^2 adsorption in the whole reaction period.The results obtained using the batch method and low techniques all implied that the different effects of sorbed phosphate would be attributed to its effects on Cu^2 ion diffusion in soil solution.     

美国大陆大气Ca2+和Mg2+复合型湿沉降对土壤无机碳固定的贡献研究

Soil inorganic carbon （SIC） stocks continuously change from the formation of pedogenic carbonates, a process requiring inputs of Ca2＋ and Mg2＋ ions. This study ranked the soil orders in terms of potential inorganic carbon sequestration resulting from wet Ca2＋ and Mg2＋ deposition from 1994 to 2003 within the continental United States. The analysis revealed that average annual atmospheric wet deposition of Ca2＋ and Mg2＋ was the highest in the Central Midwest-Great Plains region, likely due to soil particle input from loess-derived soils. The soil orders receiving the highest total average annual atmospheric wet Ca2＋ and Mg2＋ deposition, expressed as potential inorganic carbon formation （barring losses from erosion and leaching）, were： 1） Mollisols （1.1 × 10^8 kg C）, 2） Alfisols （8.4 × 10^7 kg C）, 3） Entisols （3.8 × 10^7 kg C）, and 4） Aridisols （2.8 × 10^7 kg C）. In terms of area-normalized result, the soil orders were ranked： 1） Histosols （73 kg C km-2）, 2） Alfisols and Vertisols （64 kg C km-2）, 3） Mollisols （62 kg C km-2）, and 4） Spodosols （52 kg C kin-2）. The results of this study provide an estimate of potential soil inorganic carbon sequestration as a result of atmospheric wet Ca2＋ and Mg2＋ deposition, and this information may be useful in assessing dynamic nature of soil inorganic carbon pools.     

Na~+、Ca~(2+)及Na~+-Ca~(2+)混合离子对胡敏酸胶体稳定性的影响

以胡敏酸为研究对象,通过光散射技术比较土壤中常见盐基离子(Na~+、Ca~(2+)和Na~+-Ca~(2+)混合三种电解质)不同浓度条件下胡敏酸胶体凝聚动力学过程,明确不同价态离子界面行为和陪补离子效应对胡敏酸分散稳定性和凝聚体结构的影响。结果发现,Na~+和Ca~(2+)对胡敏酸胶体聚沉能力的差异远远大于舒尔策-哈迪(Schulze-Hardy)规则中因其化合价不同所引起的差异;Na~+-Ca~(2+)混合体系中Ca~(2+)主导凝聚过程,且Na~+-Ca~(2+)混合与Ca~(2+)两种离子体系中凝聚现象的差异随离子浓度的降低而增大;混合离子体系中Na~+作为陪补离子,其陪补离子效应对临界聚沉浓度、颗粒间活化能和胡敏酸凝聚体结构均有一定影响,尤以对凝聚体的结构特征影响显著;Na~+-Ca~(2+)混合体系中胡敏酸凝聚体的结构紧实程度介于单纯离子体系之间,因此可通过调节溶液中的离子组成实现对凝聚体结构紧实程度的调控。上述结果表明,Ca~(2+)对胡敏酸的聚沉不仅依赖于静电作用,还有Ca~(2+)在强电场中的极化诱导其与胡敏酸表面含氧官能团之间发生的共价键和桥键的贡献;此外,陪补离子Na~+与Ca~(2+)在胡敏酸胶体表面的竞争吸附抑制了Ca~(2+)对胡敏酸的聚沉作用,从而形成紧实程度适中的结构体。研究结果为探究胶体界面反应及土壤胶体凝聚机制提供新的思路和理论。     

Ca2+和CaM对苹果果实Ca2+-ATPase,SOD和PEA活性的影响

采用45Ca2+ 示踪等方法研究苹果果肉质膜微囊Ca2+ ATPase与Ca2+ 运输之间的关系 ,在Ca2+ 和CaM激活剂和抑制剂存在条件下培养果实圆片 ,探索Ca2+-ATPase ,SOD和PEA活性受Ca2+和 (或 )CaM调控的可能性。结果表明 ,存在于质膜上的Ca2+-ATPase并受载体A23187刺激而活性增加 ,Ca2+-ATPase活性与Ca2+运输依抑制剂EB浓度增加而下降 ,二者变化趋势十分一致 ,从而证实了Ca2+-ATPase推动苹果果肉质膜微囊Ca2+的主动运输。果肉质膜微囊Ca2+-ATPase同时受到Ca2+和CaM调节 ,而SOD和PEA活性仅受Ca2+ 的调节 ,而与CaM无关。     

重庆渝东北植烟区土壤交换性钙镁与土壤属性的关联特性研究

为明确重庆渝东北植烟区土壤中交换性钙、镁养分状况与土壤属性的关联特性，为烟区养分管理提供参考依据，利用GPS定位技术在渝东北植烟区采集了1 092个代表性土壤样品，对巫溪、巫山、奉节、万州、涪陵和丰都6个区县植烟土壤交换性钙和交换性镁含量分析，同时与其他土壤属性进行关联分析。结果表明：重庆渝东北植烟土壤交换性钙、镁含量丰富，其平均值分别为10.85 cmol/kg和1.79 cmol/kg，但也存在缺乏现象，且区域分布不均衡。总体来看，土壤交换性钙缺乏(<6 cmol/kg)占比28.30%，土壤交换性镁缺乏(<1.0 cmol/kg)占比42.75%。涪陵县与丰都县的土壤交换性钙、镁缺乏最严重，占比分别为40.00%和55.00%。丰都县与万州区土壤交换性钙、镁含量最适宜烤烟种植，占比分别为42.00%和36.61%。母质是影响土壤交换性钙、镁含量的重要因素，二叠系泥灰岩发育形成的土壤交换性钙、镁含量较高，侏罗纪紫色砂岩含量最低。植烟土壤pH、阳离子交换量与交换性钙、镁存在显著正相关关系，而土壤交换性酸总量与二者呈显著负相关，交换性钙镁缺乏是引起烟田酸化的主要原因。1～2...     

Poorly crystalline iron and aluminium oxides contribute to the carbon saturation and sorption of dissolved organic carbon in the soil

Soil carbon (C) saturation implies an upper limit to a soil's capacity to store C depending on the contents of silt + clay and poorly crystalline Fe and Al oxides. We hypothesized that the poorly crystalline Fe and Al oxides in silt + clay fraction increased the C saturation and thus reduced the capacity of the soil to sorb additional C input. To test the hypothesis, we studied the sorption of dissolved organic carbon (DOC) on silt + clay fractions (<53 µm) of highly weathered oxic soils, collected from three different land uses (i.e., improved pasture, cropping and forest). Soils with high carbon saturation desorbed 38% more C than soils with low C saturation upon addition of DOC, whereas adsorption of DOC was only observed at higher concentration (>15 g kg^?1). While high Al oxide concentration significantly increased both the saturation and desorption of DOC, the high Fe oxide concentration significantly increased the desorption of DOC, supporting the proposition that both oxides have influence on the DOC sorption in soil. Our findings provide a new insight into the chemical control of stabilization and destabilization of DOC in soil.     

贵州烟田土壤pH、交换性钙镁和CaCO3含量分布特征及其相互关系

【目的】明确贵州烟田土壤pH、交换性钙(Ca²⁺)、交换性镁(Mg²⁺)和碳酸钙(CaCO₃)的含量分布特征及其相互关系,指导土壤酸碱调节及钙镁肥料施用。【方法】采集贵州全省烟区500个典型烟田耕层(0～20 cm)土样,采用经典方法测定土壤p H、Ca²⁺、Mg²⁺和CaCO₃含量,利用SPSS比较不同成土母质、土壤类型和区域之间pH、Ca²⁺、Mg²⁺和CaCO₃的含量差异,定量分析pH与Ca²⁺、Mg²⁺和CaCO₃之间的关系。【结果】土壤pH、Ca²⁺和Mg²⁺含量偏低的烟田分别占20.0%、18.2%和56.4%,偏高的烟田分别占37.0%、55.8%和29.6%。CaCO₃低于10 g kg^-1 烟田占88.4%。不同成土母质、...     

电位计滴定法对Co2+, Ni2+, Cu2+ and Zn2+与胡敏酸和富里酸形成复合物时的结合常数的确定

The formation constants of Co^2 ,Ni^2 ,Cu^2 and Zn^2 complexes with humic acid(HA) and fulvic acid(FA) in red soil wrer determined by the potentiometric titration method.The constants as a function of composition of the complexation solutions were obtained by two graphical approaches respetively,The formation constants decreased with increasing concentration of metal in the solution,The results provide unambiguous evidence for the heterogeneity of the function groups of humic substances,the formation constants of FA were much smaller than those of HA,and the formation constants of Cu^2 were much greater than those of Co^2 ,Ni^2 and Zn^2 ,The potentiometric titration methon for determining formation constants are also discussed in the article.     

不同橡胶生长期土壤中的微生物生物量碳和有机碳

Soil samples were collected from different rubber fields in twenty-five plots selected randomly in the Experimental Farm of the Chinese Academy of Tropical Agriculture Sciences located in Hainan, China, to analyse the ecological effect of rubber cultivation. The results showed that in the tropical rubber farm, soil microbial biomass C (MBC) and total organic C (TOC) were relatively low in the content but highly correlated with each other. After rubber tapping, soil MBC of mature rubber fields decreased significantly, by 55.5%, compared with immature rubber fields. Soil TOC also decreased but the difference was not significant. Ratios of MBC to TOC decreased significantly. The decreasing trend of MBC stopped at about ten years of rubber cultivation. After this period, soil MBC increased relatively while soil TOC still kept in decreasing. Soil MBC changes could be measured to predict the tendency of soil organic matter changes due to management practices in a tropical rubber farm several years before the changes in soil TOC become detectable.     

通过微量量热法研究Cd2+在针铁矿上的吸附机制

A study on energy changes and mechanisms of Cd sorbed on goethite was performed using the technique of microcalorimetry.The data of the amount of Cd sorpion(Aq) and concentration of Cd in equilibrium solution(Ce),and the data of Aq and the heat effect(AH) caused by Cd^2 sorption on goethite all fitted Langmuir isotherm.The amount of heat released from Cd sorption on goethite increased with the amount of Ce or Aq.The reaction process of Cd sorption on goethite may be divided into five stages and three plateaus,depending on the variation of enthalpy change(ΔaHm) of Cd sorption with Aq,which implied three mechanisms of interaction between Cd and goethite.The experimental results showed that the microcalorimetry may be useful for determination of microcalorie variation in soil.     

西藏色季拉山典型植被类型土壤活性有机碳分布特征

研究土壤活性有机碳含量及分配比例是揭示土壤有机碳库周转及调控机理的重要途径。为探讨不同森林植被类型对土壤活性有机碳库的影响,以西藏色季拉山(西坡)的高山灌丛(AS)、杜鹃林(RF)、急尖长苞冷杉林(AGSF)和林芝云杉林(PLLF)为试验对象,研究了林地土壤总有机碳、总氮含量、各活性有机碳组分及其分配比例。结果表明：高海拔植被类型具有较高的土壤活性有机碳含量和分配比例。在不同植被类型的生态系统中,土壤总有机碳含量、土壤颗粒有机碳和土壤易氧化碳含量均呈现出随土层深度增加而递减的变化趋势。土壤颗粒有机碳含量占土壤总有机碳含量和土壤易氧化有机碳含量占土壤总有机碳含量的比率范围不同,且随土层深度增加比率减小,且颗粒有机碳分配比例表现的更为明显。土壤颗粒有机碳含量和土壤易氧化有机碳含量与土壤总有机碳含量和总氮之间的相关性均达到了极显著水平(p＜0.05),土壤颗粒有机碳含量和土壤易氧化有机碳含量的相关性在在不同土层表现出显著性。