不同浸提剂以及保存方法对土壤矿质氮测定的影响

为探明影响土壤矿质氮测定的因素,从棕壤、潮土和黄棕壤3种类型土壤中各采集10个经不同施肥处理的土样,用连续流动注射分析仪测定经不同浸提剂以及不同保存方法处理后土样的NO3-N和NH4-N含量。结果表明:不论是棕壤、潮土还是黄棕壤,2 mol.L?1 KCl提取硝态氮的数量与0.01 mol.L?1 CaCl2提取的数量相关性均达到P<0.01水平;3种土壤各个土样硝态氮含量的测定值多表现为新鲜土<冷冻土<风干土;将鲜样浸提后作短时间的冷冻处理,其效果与鲜样24 h内的测定结果较接近;土样不同保存方式以及浸提液的保存时间对3种土壤NH4-N测定结果的影响规律不及NO3-N明显。     

稻菜轮作制下土壤有效态汞提取剂和提取条件研究

选择长三角地区代表性人为耕作土——青紫泥为研究对象,通过网室盆栽和室内试验,选用CaCl2,HCl,DTPA(二乙烯三胺五乙酸)和NH4OAc共4种提取剂,研究了水稻—小白菜—萝卜作物轮作系统中土壤有效态汞提取剂的选择与提取条件的优化问题。结果表明,不同提取剂提取的有效态汞含量随提取时间的延长而逐渐增加,30min可作为提取剂提取土壤有效态汞的最佳平衡时间;随土水比的减小,提取剂提取的土壤有效态汞量明显提高,1∶5为较适宜的土水比;不同提取剂的提取能力不同,对供试土壤,提取剂提取能力的大小顺序为:CaCl2>HCl>NH4OAc>DTPA。提取剂提取的土壤有效态汞量之间存在显著正相关,其中CaCl2和NH4OAc之间相关性最高;在土壤—水稻系统和土壤—萝卜系统中作物可食部位汞含量与提取剂提取的土壤有效态汞含量之间存在显著正相关关系,但在土壤—小白菜系统中相关性不强。综合分析,确定CaCl2为供试土壤汞有效态的最佳化学提取剂。     

用于表征三七种植区土壤中可利用态砷的化学提取剂的筛选

为正确表征云南文山三七种植区土壤中植物可利用态砷,选取NaH2PO4（0.5mol·L-1）、H2O、H3PO4（0.2mol·L-1）、EDTA（0.0625mol·L-1,pH=7）、NH4C（l1.0mol·L-1）和（NH4）2SO（40.05mol·L-1）6种提取剂,比较了它们对土壤中砷的提取效果,及其所提取的砷与三七植株各部位砷含量之间的相关关系。结果表明,NaH2PO4、H3PO4和（NH4）2SO4这3种提取态砷与土壤总砷呈极显著正相关,相关系数分别为0.8359、0.8177和0.8810。NaH2PO4和H3PO4的提取效率较高,平均提取效率分别为6%和11%;而（NH4）2SO4提取效率较低,平均仅为0.084%。NaH2PO4和（NH4）2SO4提取态砷与三七主根、须根和茎部砷含量呈显著正相关,H3PO4提取态砷与三七主根和须根砷含量呈显著正相关。综合考虑认为NaH2PO（40.5mol·L-1）是最佳提取剂,H3PO（40.2mol·L-1）提取剂次之,这两种提取剂均可较好地表征土壤中砷的三七可利用性。     

平衡时间及含水量对红壤有效态铅提取量的影响

比较了4种浸提剂在9种平衡时间和2种土壤含水量条件下对红壤铅的提取能力。结果表明,随着平衡时间延长和土壤含水量增加,铅提取量有逐渐增加的趋势。不同提取剂提取的有效态铅达到平衡的时间分别为HAc4小时;NH4NO32小时;HCl2小时;EDTA1.5小时。不同提取剂的提取能力不同,对于黄筋泥,其顺序为:1molL-1NH4NO3<2.5%HAc<0.05molL-1HCl<0.01molL-1EDTA;对于红砂土,其顺序为:2.5%HAc<1molL-1NH4NO3<0.05molL-1HCl<0.01molL-1EDTA。     

长江三角洲地区污水污泥与健康安全风险研究 Ⅲ. 苏、杭二城市污水污泥所施土壤中Cu和Zn的释放动态及其环境风险

未经处理的污泥农业利用后,不仅会增加土壤中污染物的含量,而且会威胁人类和其他生物的健康。室内培养试验结果表明,污泥中的重金属进入土壤后,表现出先释放,后固定的变化趋势,而且随培养时间的增加,施污泥土壤中EDTA和CaCl2提取态Cu和Zn含量逐渐增加,150d时其含量达到最高。与对照处理相比,施污泥土壤中EDTA提取态Cu和Zn含量分别增加了21.4mgkg-1和26.1mgkg-1,而CaCl2提取态Cu和Zn含量分别增加了0.10mgkg-1和3.37mgkg-1。重金属不合格的污泥农业利用存在一定程度的重金属污染风险,且其风险大小与土壤类型、污泥种类和培养时间及污泥的土壤施用量等因素密切相关。选择适宜的土壤类型、污泥种类、施用时间及控制污泥施用量等,能够在一定程度上降低污泥中重金属农业利用的环境风险。     

不同供氮水平对大葱土壤硝态氮运移及品质影响的研究

在山东省章丘大葱/小麦轮作典型种植制度下,研究了不同施氮量对土壤硝酸盐及大葱品质影响。研究表明:章丘地区大葱地硝酸盐淋洗较严重。大葱各生长发育时期测得处理T5土壤硝态氮含量与T1之间的差异都达到极显著水平;收获时处理T5的0～30cm、30～60cm、60～90cm三个耕层土壤硝态氮残留量分别为4.35mgkg-1、6.81mgkg-1和6.49mgkg-1,可见该处理施氮量已远超出大葱正常生长所需。大葱产量以氮素优化处理(T4)最高,与T5间的差异也达到显著水平;同时该处理大葱硝态氮含量与T5间的差异也达到极显著水平。大葱Vc和可溶性糖含量都是对照最高,随施氮量的增加两者含量逐渐降低。     

土壤有效态重金属提取剂选择的研究

利用5种不同的土壤重金属浸提剂,研究了土壤有效态重金属含量与玉米重金属含量的关系,并提出了一种新的土壤有效态重金属的浸提剂。结果表明:0.1mol/L HCl,0.05mol/L EDTA-2Na,0.1mol/L CaCl2,0.1mol/L HAc-NaAc,0.05mol/L DTPA提取的化学有效态重金属与玉米根、茎、叶中重金属Cu、Zn、Cd、Pb大部分呈显著或极显著相关,但各化学提取剂提取的有效态Zn、Cu与玉米籽粒Zn、Cu的相关性较差。利用柠檬酸-酒石酸为提取剂提取的重金属含量与玉米籽粒中重金属的含量有着相对较好的相关性,是一种预估玉米籽粒中重金属含量的较好办法。     

炭输入及生化调控对设施菜田土壤N_2O排放的影响

本研究以河北永清蔬菜基地设施菜田土壤为研究对象,控制温度(25±1)℃和土壤含水量(70%WFPS),采用静态培养方法,通过监测培养期间土壤N_2O排放通量、无机氮含量及土壤中酶活性的变化情况,研究炭输入及生化调控对设施菜田N_2O排放及氮素转化的影响。结果表明,土壤添加尿素后,N_2O排放峰值达到644.11μg N·kg~(-1)·d~(-1),添加双氰胺(DCD)和石灰氮(CaCN_2)的土壤N_2O排放峰值分别为101.47μg N·kg~(-1)·d~(-1)和36.74μg N·kg~(-1)·d~(-1),对于N_2O减排效果好,且能有效抑制亚硝态氮的产生;施用控释尿素、添加黑炭或有机肥能减少N_2O排放,而添加石灰氮闷棚显著增加了N_2O排放。控释尿素、秸秆、黑炭、DCD和CaCN_2均对铵态氮向硝态氮的转化有一定抑制作用,施加石灰氮或有机肥有助于减少硝态氮向亚硝态氮的转化。相关分析表明,土壤中硝态氮和亚硝态氮含量增加,有助于反硝化过程的进行,增加了N_2O排放的风险。     

封育对蒿类荒漠草地土壤氮素含量及其组分特征的影响

为探讨蒿类荒漠草地土壤氮素含量及其组分特征,采用成对试验设计,研究封育对天山北坡不同区域蒿类荒漠草地土壤全氮、碱解氮、硝态氮和铵态氮含量的影响。结果表明:(1)封育后蒿类荒漠草地0—50 cm土层土壤氮密度(0.59~0.79 kg/m²)、土壤全氮含量(0.81~1.50 g/kg)、土壤碱解氮含量(19.44~67.49 mg/kg)变化不显著(p＞0.05)。(2)封育对蒿类荒漠草地土壤硝态氮含量(6.41~21.26 mg/kg)、铵态氮含量(0.26~2.53 mg/kg)的影响因区域差异而有所不同。封育后巩留、呼图壁样地0—50 cm土层硝态氮含量依次显著降低24.61%,47.25%(p＜0.01),而奇台样地则显著增加20.95%(p＜0.05);封育后玛纳斯样地0—50 cm土层铵态氮含量显著增加27.98%(p＜0.05),而巩留、博乐、呼图壁样地则降低不显著(p＞0.05)。(3)蒿类荒漠草地土壤硝态氮、铵态氮含量依次占全氮量的0.27%~3.01%,0.02%~0.42%,且随土壤全氮的增加,有机氮占比增加,而无机氮、硝态氮和铵态氮占比降低。(4)相关分析表明,土壤全氮、碱解氮、硝态氮、铵态氮与有机碳、全磷呈正相关,与土壤容重、pH、电导率呈负相关,铵态氮与土壤含水量呈正相关,与速效磷呈负相关。偏冗余分析表明,土壤理化因子对土壤氮素影响的主要因子为土壤有机碳和土壤含水量,解释率依次为32.60%,17.90%。研究结果为揭示封育过程中蒿类荒漠草地土壤恢复及养分管理提供科学数据支撑。     

设施蔬菜土壤剖面氮磷钾积累及对地下水的影响

针对设施栽培中传统施肥灌溉带来的养分浪费和环境污染问题,采集河北省定州市设施蔬菜、农田土样及相应的地下水样品,分析了不同设施蔬菜种植年限土壤剖面中速效养分的累积规律及地下水受硝酸盐污染的程度。结果表明:0～200cm和0～400cm设施土壤的速效养分累积均高于对照农田。低龄棚硝态氮、速效磷、速效钾及水溶性磷含量分别为377.2mg·kg-1、448.8mg·kg-1、1405.6mg·kg-1、30.6mg·kg-1,分别是对照农田的4.7倍、4.6倍、1.4倍和11.5倍;老龄棚硝态氮、速效磷、速效钾及水溶性磷含量分别为629.1mg·kg-1、555.0mg·kg-1、2567.1mg·kg-1、35.2mg·kg-1,分别为对照农田的6.4倍、16.3倍、2.7倍和12.0倍。设施土壤速效养分深层累积比例随棚龄增加而增加。设施蔬菜栽培区表层地下水(地下饮用水,20m)受硝态氮污染严重,超标率和严重超标率为39.3%和7.1%;而深层地下水(农田和大棚灌溉水,40m)硝态氮含量7.4mg·L-1和9.6mg·L-1,超标率分别为25.0%和37.5%,无严重超标水样。     

Development and Validation of a New Soil Universal Extractant: 0.02 Molar Strontium Chloride

Abstract

In this experiment, when the strontium chloride–citrate acid extractant (0.02 M SrCl₂–0.05 M citrate) was used for extraction of calcareous soils with calcium carbonate greater than 70 g kg^?1, the filtrate was turbid. Furthermore, white precipitation appeared when this extract was used for phosphorus determination with the Murphy and Riley method. As the concentration of citrate in strontium chloride–citrate acid extractant decreased to 0.025 or 0 M, the filtrate became clean. Further experiments indicated that the 0.02 M SrCl₂ extractant could be used as a universal extractant for soil nitrate+nitrite and potassium; the extracted nitrate+nitrite and potassium significantly correlated with nitrogen and potassium phytoavailability, respectively, determined with ryegrass pot experiment (P<0.05). Thus, the 0.02 M SrCl₂ was recommended as a universal extractant for soil nitrate+nitrite and potassium.     

腐殖酸对磷在红壤中有效性的影响

An investigation was conducted to study the effect of humic substance （HS） on the phosphorus （P） solubility in acidic soil. The soil （2.5 g）, HS （0, 0.5, and 2.5 g）, and P as monocalcium phosphate （0.31 and 1.25 g P kg^-1 soil） were mixed with 50 mL distilled water and two different sequences of adding HS and P were used. The results indicated that the P concentration in water and 0.01 mol L-1 CaCl2 solution increased with increasing amounts of humic substance. The concentrations of Fe and Al were also increased. However, Olsen P decreased with increasing amount of humic substance. Water-soluble P concentrations from P rates at 0.31 and 1.25 g P kg^-1 soil in the treatment with 0.5 g （2.5 g） humic substance addition were 360% and 70% （500% and 90%） higher, respectively, than those in the treatment with no humic substance addition. P extracted by 0.01 mol L^-1 CaCl2 in the treatments with 0.5 and 2.5 g humic substance addition was increased by 400% and 540%, respectively, compared with that in the treatment without humic substance at the rate of 0.31 g P kg^-1 soil, while the corresponding P concentrations were increased by 80% and 90% at the rate of 1.25 g P kg^-1 soil. The order of mixing humic substance and phosphate did not significantly affect desorbed P and labile P extracted with CaCl2.     

苏南地区土壤重金属向蔬菜的迁移研究

Vegetable fields in peri-urban areas receive large amounts of extraneous heavy metals because of rapid urbanization and industrialization in China. The concentrations of Cu, Zn, and Pb in 30 soil samples and 32 vegetable samples, collected from 30 different sites in southern Jiangsu Province of China, were measured and their transfer from soil to vegetable was determined. The results showed that the soil samples had wide ranges of pH (4.25-7.85) and electrical conductivity (EC) (0.24-3.42 dS m^-1). Among the soil samples, there were four soil samples containing higher Cu and two soil samples containing higher Zn concentrations than those specified in the Chinese Soil Environmental Quality Standard II. However, no vegetable sample was found to contain a high level of Cu or Zn. In contrast, one vegetable sample contained 0.243 mg Pb kg^-1 FW, which was above the Chinese Food Hygiene Standard, whereas the corresponding soil Pb concentration was lower than the Chinese Soil Environmental Quality Standard II. The transfer coefficients of Cu of all vegetable samples exceeded the suggested coefficient range, implying that extraneous Cu had high mobility and bioavailability to vegetables. There was no significant correlation between extractable soil heavy metal concentrations with four kinds of extractants and soil pH, EC, heavy metal concentrations in vegetables and soils, except that soil pH correlated well with the extractable soil Cu, Zn, and Pb concentrations with 1.0 mol L^-1 NH₄NO₃. Moreover, diethylenetriamine pentaacetic acid (DTPA) extraction method was a more effcient method of extracting heavy metals from the soils independent of soil pH and EC than other three methods used.     

长期使用含铜杀真菌剂对苹果园土壤中自由态铜离子、固相铜形态分级以及微生物活性的影响

Soil samples were collected from apple orchards 5,15,20,30,and 45 years old,and one adjacent forest soil was used as reference to investigate the free Cu2+ion activity in soil solution and the soil Cu fractionation in the solid phase following long-term application of copper fungicide,Bordeaux mixture,in apple orchards and to investigate the relationships among soil free Cu2+ions,Cu fractionation and soil microbial parameters.The total Cu concentration in the orchard soils varied from 21.8 to 141 mg kg-1,increasing with the orchard age,and the value for the reference soil was 12.5 mg kg-1.The free Cu2+ion concentrations in the soil solutions extracted by 0.01 mol L-1 KNO3 ranged from 3.13×10-8(reference)to 4.08×10-6 mol L-1(45 years-old orchard).The concentration of Cu complexed in the fulvic fraction increased with orchard age from 5.16 to 52.5 mg kg-1.This was also the case for other soil Cu fractions except the residual one.The residual soil Cu remained practically constant,ranging from 4.28 to 5.66 mg kg-1,suggesting that anthropogenic soil Cu mainly existed in the more labile active fractions.Regression analyses revealed that both the free Cu2+ions in the soil solution and the humic acid-complexed Cu fraction in the solid phase were strongly related with soil microbial parameters.     

石灰性土壤有效硒浸提剂和浸提条件研究

采用外源硒加入土壤中得到硒污染土壤,6种有效硒的浸提剂NaHCO3、KH2PO4、K2SO4、EDTA、AB-DTPA和DTPA＋TEA＋CaCl2的最佳浸提时间和土液比进行了筛选,并通过盆栽试验对所选择的土壤有效硒浸提剂进行生物学校验,以找出石灰性土壤有效硒提取适宜的浸提剂及其浸提条件。结果表明,NaHCO3、KH2PO4、K2SO4、EDTA、AB-DTPA和DTPA＋TEA＋CaCl26种浸提剂有效硒浸提量都随着浸提土液比的减小而增大,且随浸提时间的增长而增大。其中NaHCO3和KH2PO4最佳土液比为1/15,振荡时间90min;K2SO4和AB-DTPA的最佳土液比为1/15,振荡时间60min;EDTA和DTPA＋TEA＋CaCl2的最佳土液比则为1/20,振荡时间30min。6种浸提剂在各自最佳的提取条件下提取的土壤有效硒量与白菜地上部分硒含量达极显著正相关,但土壤有效硒的提取量以DTPA＋TEA＋CaCl2及K2SO4最少,只占KH2PO4、AB-DTPA及EDTA提取量的14%～48%,故不适用于作为石灰性土壤有效硒的提取剂。NaHCO3适用于土壤硒含量高于5mg·kg^-1的石灰性土壤有效硒提取。KH2PO4、AB-DTPA及EDTA3种浸提剂既可提取土壤中水溶态硒,亦可提取部分的吸附态硒,提取硒数量较多,过程简单,重复性好,都可作为石灰性土壤有效硒提取的浸提剂。     

酸性土壤有效汞提取方法研究

为了更好地评价酸性土壤中汞的生物有效性和生态风险,以酸性土壤为供试土壤,通过比较国内外几种常用的土壤有效汞的浸提剂的提取效果,筛选适合于酸性土壤的有效汞浸提剂并优化相应的提取条件,从而建立酸性土壤有效汞的提取方法。结果表明,在0.1 mol·L-1HCl、1 mol·L-1NH4OAc、0.005 mol·L-1DTPA、0.03%TGA-1/15 mol·L-1Na2HPO4这4种常用浸提剂中,0.03%TGA-1/15 mol·L-1Na2HPO4是最佳的浸提剂,因为它具有最高的提取率,且其所提取的有效汞与相应稻米中Hg含量的相关性最好。0.03%TGA-1/15 mol·L-1Na2HPO4的最佳浸提条件为土液比1∶10、振荡时间120 min、振荡速度250 r.min-1,浸提出的有效汞量与油菜的相关性达到极显著相关,能较好地指示田间条件下土壤汞对作物的可给性。