稻麦轮作条件下长期不同土壤管理对磷、钾和pH的影响

免耕土壤速效磷含量在整个面均低于耕翻土壤；0～5cm土壤生物量磷含量免耕高于耕翻，5～15cm免耕低于耕翻；施肥和休闲土壤均维持了较高的有效磷和生物量磷水平。种植作物的免耕土壤缓效钾含量与耕翻土壤没有显差异，0～5cm速效钾含量呈免耕高于耕翻的趋势，休闲的免耕土壤整个剖面缓效钾和速效钾含量都高于耕翻；免耕土壤缓效钾的分布无明显的层次性，速效钾则相反；施肥明显提高土壤速效钾含量，但对缓效钾的影响不大。长期免耕没有导致土壤酸化；免耕土壤pH与耕翻土壤没有差异。     

典型黑土pH值变化对微量元素有效态含量的影响研究

采用室内培养实验的方法 ,控制典型黑土样品的酸碱度值 ,探讨典型黑土中 Cu、Zn和 Mn等微量元素有效态含量与 p H值的关系。结果表明 :p H值变化 0 .5个单位左右 ,有效态铜含量变化约 0 .5～ 1倍 ;有效态锰含量变化约 3～ 5倍 ;有效态锌含量变化 9～ 1 5倍之多。说明精确掌握土壤的酸碱度值对于土壤诊断、微肥的合理施用、提高作物产量和实现土地的可持续利用都具有重要的理论与实践意义     

恒pH自动滴定系统及其在土壤表面化学研究中的应用

利用MIA 3型自动分析系统的硬件 ,根据研究的需要开发了一个专用软件 ,建成适用于恒pH自动滴定系统。并对一个含氧化铁很高的砖红壤的表面羟基的释放过程进行了测试应用。结果显示 ,在Na2 SO4 溶液中 ,羟基释放量明显受pH和SO2 - 4加入量的影响 ,羟基释放量的动态变化很好地符合Elovich方程。     

恒电荷土壤及可变电荷土壤与离子间相互作用的研究 I.共存离子对NO_3~-吸附的影响

研究了我国典型３种可变电荷土壤和４种恒电荷土壤在陪伴阳离子分别为Ｋ十、Ｎａ十、Ｃａ２＋时和１ｍｍｏｌＬ－１ＫＣ１、Ｋ２ＳＯ４支持电解质中ＮＯ３－的吸附。结果表明，ＮＯ３－吸附量随ｐＨ的增加而减小。在添加相同浓度ＮＯ３－时，３种可变电荷土壤对ＮＯ３－的吸附量顺序为Ｃａ（ＮＯ３）２＞ ＫＮＯ３＞ＮａＮＯ３＞ＫＮＯ３十ＫＣＩ＞ＫＮＯ３＋Ｋ２ＳＯ４；在初始ＮＯ３－浓度０．５－５ｍｍｏｌＬ－１的范围内，吸附量随浓度变化的关系符合Ｌａｎｇｍｕｉｒ等温吸附式．由此求出与ＮＯ３－吸附结合能有关的常数（Ｋ）在不同共存离子存在下数值较小且差异不大，因此认为不同陪伴阳离子和不同伴随阴离子对ＮＯ３－吸附的电性机理影响不大，只是改变了土壤表面的正电荷数量从而使吸附量发生变化。４种恒电荷土壤对ＮＯ３－的吸附量通常很小，其中在Ｃａ（ＮＯ３）２介质中较在其他介质中稍大，最大吸附量仅为１．５～ｍｍｏｌ ｋｇ－１左右，约为可变电荷土壤的１／１０，且在浓度较低时常观察到负吸附。     

The N2O product ratio of nitrification and its dependence on long-term changes in soil pH

The contribution of nitrification to the emission of nitrous oxide (N₂O) from soils may be large, but its regulation is not well understood. The soil pH appears to play a central role for controlling N₂O emissions from soil, partly by affecting the N₂O product ratios of both denitrification (N₂O/(N₂+N₂O)) and nitrification (N₂O/(NO₂⁻+NO₃⁻). Mechanisms responsible for apparently high N₂O product ratios of nitrification in acid soils are uncertain. We have investigated the pH regulation of the N₂O product ratio of nitrification in a series of experiments with slurries of soils from long-term liming experiments, spanning a pH range from 4.1 to 7.8. ¹⁵N labelled nitrate (NO₃⁻) was added to assess nitrification rates by pool dilution and to distinguish between N₂O from NO₃⁻ reduction and NH₃ oxidation. Sterilized soil slurries were used to determine the rates of chemodenitrification (i.e. the production of nitric oxide (NO) and N₂O from the chemical decomposition of nitrite (NO₂⁻)) as a function of NO₂⁻ concentrations. Additions of NO₂⁻ to aerobic soil slurries (with ¹⁵N labelled NO₃⁻ added) were used to assess its potential for inducing denitrification at aerobic conditions. For soils with pH?5, we found that the N₂O product ratios for nitrification were low (0.2-0.9‰) and comparable to values found in pure cultures of ammonia-oxidizing bacteria. In mineral soils we found only a minor increase in the N₂O product ratio with increasing soil pH, but the effect was so weak that it justifies a constant N₂O product ratio of nitrification for N₂O emission models. For the soils with pH 4.1 and 4.2, the apparent N₂O product ratio of nitrification was 2 orders of magnitude higher than above pH 5 (76‰ and 14‰). This could partly be accounted for by the rates of chemodenitrification of NO₂⁻. We further found convincing evidence for NO₂⁻-induction of aerobic denitrification in acid soils. The study underlines the role of NO₂⁻, both for regulating denitrification and for the apparent nitrifier-derived N₂O emission.     

Optimization of hydrolytic and oxidative enzyme methods for ecosystem studies

Microbial digestive enzymes in soil and litter have been studied for over a half century, yet the understanding of microbial enzymes as drivers of ecosystem processes remains hindered by methodological differences among researchers and laboratories. Modern techniques enable the comparison of enzyme activities from different sites and experiments, but most researchers do not optimize enzyme assay methods for their study sites, and thus may not properly assay potential enzyme activity. In this review, we characterize important procedural details of enzyme assays, and define the steps necessary to properly assay potential enzyme activities in environmental samples. We make the following recommendations to investigators measuring soil enzyme activities: 1) run enzyme assays at the environmental pH and temperature; 2) run proper standards, and if using fluorescent substrates with NaOH addition, use a standard time of 1 min between the addition of NaOH and reading in a fluorometer; 3) run enzyme assays under saturating substrate concentrations to ensure V_max is being measured; 4) confirm that product is produced linearly over the duration of the assay; 5) examine whether mixing during the reaction is necessary to properly measure enzyme activity; 6) find the balance between dilution of soil homogenate and assay variation; and 7) ensure that enzyme activity values are properly calculated. These steps should help develop a unified understanding of enzyme activities in ecosystem ecology.     

Extractability of cellulases in forest litter and soil

Summary Cellulases in forest litter and soil occur in both bound and extractable forms. The proportion of total bound endocellulase activity (not extractable) increases during decomposition, whereas the proportion of bound exocellulase activity remains fairly constant. The proportions of bound enzymes differ among litter types with different chemical compositions. The proportion of bound activity is higher in mineral soil than in litter. We also investigated the effects of anion type (NaCl versus Na₂SO₄), concentration and pH on the extractability of cellulases and protein in two horizons of two forest soils. The extractability of cellulases increases as pH increases from 3.5 to 5.6. Anion type and concentration did not have consistent effects on extractability. However, there was a trend for higher extractability by sulfate than by chloride and with increasing salinity.     

典型黑土pH值变化对营养元素有效态含量的影响研究

采用室内培养实验的方法,控制典型黑土样品的酸碱度值,探讨典型黑土中Cu、Zn、Mn、P和Fe等营养元素有效态含量与pH值的关系。结果表明:pH值变化0.5个单位左右,有效态铜含量变化约0.5～1倍;有效态锰含量变化约3～5倍;有效态锌含量变化9～15倍之多;有效态磷含量变化约1.5～2倍;有效态铁含量变化约3～4倍。说明精确掌握土壤的酸碱度值对于土壤诊断、合理施肥、提高作物产量和实现土地的可持续利用都具有重要的理论与实践意义。     

施氮对茶园土壤氟和茶树新梢氟含量的影响

通过田间试验研究了不施肥(CK)、施氮360 kg?hm?2(T1)、施氮720 kg?hm?2(T2)处理下茶园土壤无机氮、p H、各形态氟含量的动态变化和春、夏、秋茶树新梢一芽四叶、一芽五叶氟含量,探讨茶园施氮对土壤和茶树新梢氟含量的影响。结果表明:1)茶园施氮后短期内(20~30 d)土壤水溶态氟含量显著降低,土壤交换态氟和铁锰结合态氟含量降低;长期(45~50 d)土壤水溶态氟含量的降低作用减弱,土壤交换态氟和铁锰结合态的含量增加;在试验结束时(164 d),与CK处理相比,T1处理0~20 cm土壤各形态氟含量降低,T2处理0~20 cm土壤各形态氟含量增加。2)0~20 cm茶园土壤水溶态氟、铁锰结合态氟与NH4+-N分别呈极显著负、正相关(P0.01),20~40 cm土壤水溶态氟、交换态氟与NO3?-N分别呈极显著正、负相关(P0.01)。土壤p H与土壤水溶态氟含量极显著负相关(P0.01),与其他3种形态氟含量相关性不显著。土壤铁锰结合态氟与交换态氟、有机结合态氟呈显著、极显著正相关,但与土壤水溶态氟均无显著相关性。3)春茶前后施氮可以降低春、夏、秋茶树新梢一芽四叶、一芽五叶氟含量,但未达显著水平。T1处理新梢氟含量的降低值为夏茶(25.15~27.95 mg?kg?1)秋茶(21.06~24.31 mg?kg?1)春茶(18.58~21.03 mg?kg?1),T2处理的降低值为秋茶(18.64~22.34 mg?kg?1)夏茶(7.79~14.14 mg?kg?1)春茶(3.52~7.30 mg?kg?1)。春、夏、秋茶树新梢氟含量主要受0~20 cm土壤无机氮和20~40 cm土壤p H的影响。因此推测施氮通过影响茶树根系氟的吸收和氟在叶片中的累积过程调控茶树新梢氟含量,该研究成果为合理利用施氮技术降低茶园土壤和茶树新梢氟含量提供了理论依据。