水溶性有机质对土壤吸附有机污染物的影响

在自然环境中,水溶性有机质(DOM)会对土壤吸附有机污染物产生影响.基于已有的成果,本文综合分析了DOM的有关因素对土壤吸附有机污染物的影响.研究表明,不同来源的DOM的亲疏水组分比例不同;随着腐解时间的增长,亲水组分减小,疏水组分增加.外源DOM的极性与亲疏水组分所含官能团的种类和数量、分子量均会影响有机污染物的吸附;DOM的临界值浓度与土壤有机质含量负相关.当DOM浓度大于临界值时抑制吸附,反之促进吸附.DOM具有酸碱缓冲作用,影响土壤溶液的pH,进而影响对有机污染物的吸附.由于土壤内源DOM对有机污染物具有增溶作用,会抑制土壤吸附有机污染物.论文最后对今后的相关研究方向提出了建议.     

安徽省土壤中氟分布的研究

安徽省２２９个土壤剖面土壤总氟和土壤水溶性氟含量测定数据表明,５个地理分区之间土壤总氟差异不大,Ａ层和Ｃ层均值分别为５２２ｍｇ／ｋｇ和６０４ｍｇ／ｊｋｇ而土壤水溶性氟在不同地区之间的差异显著,其分布规律是自北向南降低;淮北平均〉江淮丘陵〉沿江平原〉皖南地区〉大别山区。     

水溶性有机质对土壤硝化作用过程的影响

以江苏省宿迁市潮土为供试土壤,设置DOC220、DOC440和DOC880 3个添加水溶性有机质(DOM)处理,分别含有机碳(DOC)220、440和880 mg.L-1。试验结果表明,DOM对硝化过程有一定的抑制作用,在培养第16天时,未添加DOM的对照中NH4 -N几乎100%已经转化为NO3--N,而添加DOM的3个处理硝化率分别比对照降低7.83%、13.60%和19.12%;与对照相比,添加DOM的处理中NH4 -N含量降低缓慢,但培养过程中亚硝酸盐的积累显著增加,对照在第12天时NO2--N达到最大积累量67.83 mg.L-1,而DOC220、DOC440和DOC880处理土壤中NO2--N积累量分别在第12、14和16天达到最大值,与对照相比积累量分别增加21.17%、33.91%和59.90%。此外,DOM的添加也降低了NO3--N的生成速率,到第16天时,对照已经达到最大积累量143.61 mg.L-1NO3--N,但此时DOC220、DOC440和DOC880处理中NO3--N含量比对照分别低41.97、78.09和91.30 mg.L-1。为排除因添加DOM带来外源氮所引起的影响,同时进行了相同初始氮量下添加DOM与单施(NH4)2SO4对硝化作用影响的比较试验,结果同样表现出亚硝酸盐积累量的增加和NO3--N生成速率的降低,表明DOM中所含的有机碳及小分子化合物影响了硝化作用。高有机质环境下存在潜在的亚硝酸盐积累风险,对土壤和水体生态系统健康可能有一定影响。     

土壤中水溶性有机碳与铜的相互影响

通过向土壤溶液中加入Ｃｕ２＋和可溶性有机碳(ＤＯＣ),研究它们之间的相互作用．结果发现,加入铜可以显著改变土壤水溶性有机碳(ＷＳＯＣ)的吸着平衡,并降低了其水溶性．影响程度在０．８ｍｍｏｌ·ｌ－１Ｃｕ以下随铜浓度的增加而增加．加入０．５ｍｍｏｌ·ｌ－１铜的土壤中 ＷＳＯＳ含量从 ０．２７ｍｇ Ｃ·ｇ－１降至０．０４７ｍｇ Ｃ·ｇ－１,吸着系数从６．６×１０－３ｌ·ｇ－１降至３．３×１０－３ｌ·ｇ－１．另一方面,用Ｆｒｅｕｎｄｌｉｃｈ方程描述铜离子在土壤中的吸附行为(液相浓度单位取ｍｍｏｌ·ｌ－１,固相浓度取ｍｍｏｌ·ｇ－１土),ｋ＝９．ｌ×１０－３;ｎ＝３．４０． 加入ＤＯＣ后,ｋ＝９．２×１０－３;ｎ＝３．６６,没有明显改变土壤对铜的吸附性能．加入小同浓度的ＤＯＣ,结果仍说明该浓度范围内ＤＯＣ(＜８ｍｇ Ｃ·ｌ－１)的加入没有明显改变土壤对铜的吸附性能．     

土壤水溶性有机碳的研究进展

综述了土壤中水溶性有机碳的组成和来源，水溶性有机碳的含量及其影响因素，水溶性有机碳对土壤中一些无机离子的吸附以及对农药、重金属在土壤中迁移的影响等，并提出有待于进一步研究的一些问题。     

秸秆不同还田方式对土壤中溶解性有机碳的影响

土壤溶解性有机质及其可利用性与土壤质量密切相关。通过研究秸秆不同还田方式(粉碎还田、覆盖还田、高茬还田)对农田土壤溶解性有机碳的影响,探讨了土壤溶解性有机碳对土壤质量的贡献。水溶性有机碳(WSOC)和热水溶性有机碳(HWSOC)通过冷水和热水提取获得。结果表明:秸秆还田能够增加土壤有机质的含量,影响土壤中水溶性有机碳和热水溶性有机碳的含量。在粉碎还田、覆盖还田、高茬还田处理中,粉碎还田的农田土壤中WSOC和HWSOC的含量比覆盖还田、高茬还田的高,粉碎还田的农田土壤中的WSOC和HWSOC占土壤有机碳的百分比也最高。另外,WSOC和HWSOC与土壤呼吸有很好的相关性(相关系数分别为0.75,0.85)。     

安徽省土壤中氟分布的研究

安徽省２２９ 个土壤剖面土壤总氟和土壤水溶性氟含量测定数据表明,５ 个地理分区之间土壤总氟差异不大,Ａ 层和Ｃ层均值分别为５２２ ｍ ｇ／ｋｇ 和６０４ ｍ ｇ／ｋｇ;而土壤水溶性氟在不同地区之间的差异显著,其分布规律是自北向南降低：淮北平原＞ 江淮丘陵＞ 沿江平原＞ 皖南山区＞ 大别山区。土壤总氟与土壤水溶性氟无相关性。     

低分子有机酸对土壤氟吸附的影响

用等温平衡吸附法研究了柠檬酸、草酸对砂姜黑土和潮土氟吸附的影响 ,提出了有机酸影响氟吸附的可能机理。实验结果表明 ,有机酸对土壤氟吸附有较大的影响 :(1)当有机酸处于低浓度时 ,土壤氟吸附量随浓度升高而增加 ;高浓度时 ,土壤氟吸附量随有机酸浓度升高而降低 ;(2 )在有机酸存在条件下 ,土壤氟的吸附量与平衡氟浓度间呈极显著的直线正相关或负相关     

安徽省长江以北地区土壤水溶性氟含量及分布特征

采集安徽省长江以北地区有代表性土壤样品３４７个，测定了其水溶性氟含量。结果表明，土壤水溶性氟含量范围０３８～１２６９ｍｇ／ｋｇ，平均为２３８ｍｇ／ｋｇ。地区分布是南低北高，以淮北宿州和阜阳地区为最高，平均含量在３ｍｇ／ｋｇ以上。主要土壤类型土壤水溶性氟含量顺序是砂姜黑土、潮土＞黄棕壤、紫色土＞水稻土＞石灰土、粗骨土。不同母质土壤水溶性氟含量顺序是古黄土性河湖相沉积物＞黄泛冲积物＞紫色砂岩＞下蜀黄土＞石灰岩＞酸性结晶岩风化物＞河流冲积物。土壤水溶性氟含量与土壤ｐＨ呈正相关。ｐＨ高的黄泛冲积物和古黄土性河湖相沉积物母质土壤含水溶性氟多，该土壤地区发生氟中毒可能性较大。     

不同有机物料在潮棕壤中有机碳分解进程

用尼龙网袋法研究了特定年度中，不同月份间有机物料在潮棕壤旱田、水田中有机碳分解速率及C／N变化。结果表明，4种物料(玉米秸和玉米根，水稻秸和水稻根)在潮棕壤地区温度、湿度适宜的前3个月(1999年7—月)迅速分解，之后进入缓慢分解阶段，其中根的分解残留率始终高于秸秆。经计算约有2／3的玉米根和稻根腐解产物残留在土壤里；分解至试验结束。所有物料的C/N比都趋于一致，约在10—13之间，与土壤腐殖质的洲比非常相近，说明这些物料已基本完成其腐殖化过程，而成为较稳定的有机组分、这对增加土壤有机质、培肥土壤非常重要。     

可溶性有机物对土壤中主要有机污染物环境行为的影响

概括了环境中可溶性有机物的特点，并系统总结了当前国内外关于可溶性有机物对土壤中主要污染物环境行为的影响的研究进展。阐述了可溶性有机物对农药、多环芳烃在土壤中的吸附、解吸及分配等环境行为所起的作用。最后指出了该方面研究存在的问题及今后应加强的方向。     

Effects of organic matter on the specific adsorption of heavy metals by soil

The adsorption of heavy metals on soil from the Neihu Landfill Site in Taipei City was investigated in order to assess the groundwater pollution problems. The effects of soil organic matter and the behaviors of organic complexing ligands like EDTA and humic acid to the overall adsorption process were studied and discussed. For explaining the results, the pH value of soil system and the properties of the soil/aqueous interface were chosen as two significant and interacted factors for discussion. The concept of the specific adsorption mechanism was also demonstrated and discussed. The results showed that the complexing ligands existing in soil liquid phase have more influences than natural organic matter does. The competitive sequences of different organic matter contents indicated that organic functional sites preferentially bind with Cu and Cd. The presence of EDTA and humic acid which formed ligandlike complexes will reduce Cd adsorption efficiency. These effects will induce mobility and the fate of heavy metals in soils, such as bioavailability.     

Diazinon leaching through a sandy soil amended with different humic materials

The water leaching of diazinon (O,O‐diethyl‐O‐2‐isopropyl‐6‐methylpyrirnidin‐4‐yl phosphoroth‐ioate) through soil columns, was studied after column amendments with two well characterized humic acids (HA), in both liquid and solid state, and with the original raw organic materials, an oxidized coal and a leonardite, from which the HA were extracted. The percolation curves and the pesticide distribution over the soil columns showed that the addition of the raw organic materials and the solid HAs reduced significantly the mobility of the pesticide along the soil column. The oxidized coal was more effective than the leonardite original material; the different origin of the two carbon‐rich materials had an influence on the diazinon movement along the soil columns and such difference was enhanced with increasing addition rates. Moreover, incubation at field capacity for two months of the soil columns treated with raw oxidized coal and leonardite, largely enhanced the described effects on pesticide behaviour. A complete adsorption of diazinon on columns and a practical absence of leaching was observed when the HA from both materials were added in dissolved form. These results were explained with the swelling of the humic micelles in water and the enhanced availability of inner hydrophobic surfaces for the strong adsorption of diazinon. The water diffusion into the solid humic materials after two months incubation, also explains their high pesticide retention capacity. This work indicates the usefulness of either solid o dissolved humic substances, with the proper hydrophobic character, in preventing the vertical leaching of non‐polar organic pesticides in soils.     

SOMPROF: A vertically explicit soil organic matter model

Most current soil organic matter (SOM) models represent the soil as a bulk without specification of the vertical distribution of SOM in the soil profile. However, the vertical SOM profile may be of great importance for soil carbon cycling, both on short (hours to years) time scale, due to interactions with the soil temperature and moisture profile, as well as on long (years to centuries) time scale because of depth-specific stabilization mechanisms of organic matter. It is likely that a representation of the SOM profile and surface organic layers in SOM models can improve predictions of the response of land surface fluxes to climate and environmental variability. Although models capable of simulating the vertical SOM profile exist, these were generally not developed for large scale predictive simulations and do not adequately represent surface organic horizons. We present SOMPROF, a vertically explicit SOM model, designed for implementation into large scale ecosystem and land surface models. The model dynamically simulates the vertical SOM profile and organic layer stocks based on mechanistic representations of bioturbation, liquid phase transport of organic matter, and vertical distribution of root litter input. We tested the model based on data from an old growth deciduous forest (Hainich) in Germany, and performed a sensitivity analysis of the transport parameters, and the effects of the vertical SOM distribution on temporal variation of heterotrophic respiration. Model results compare well with measured organic carbon profiles and stocks. SOMPROF is able to simulate a wide range of SOM profiles, using parameter values that are realistic compared to those found in previous studies. Results of the sensitivity analysis show that the vertical SOM distribution strongly affects temporal variation of heterotrophic respiration due to interactions with the soil temperature and moisture profile.     

表面活性剂及水溶性有机物对菲生态毒性的影响

采用室内培养试验及化学试验研究了表面活性剂及水溶性有机物(DOM)对土壤中菲对小麦的生态毒性的影响.结果表明,绿肥和猪粪堆肥DOM具有具有类似表面活性剂的表面活性性质,且猪粪堆肥的表面活性较大;在本试验条件下,DOM对菲对小麦的生态毒性有减轻作用,而表面活性剂对菲生态毒性有增加的趋势;当DOM和表面活性剂共存时,菲的生态毒性则比DOM单独作用时的结果强,而弱于表面活性剂单独作用的结果.     

红树植物凋落叶分解对土壤可溶性有机质的影响

研究红树林湿地土壤可溶性有机质（DOM）的来源、性质及其归宿对于揭示 DOM 在红树林湿地生物地球化学循环中的作用具有重要意义。采集了木榄（Bruguiera gymnoihiza）、秋茄（Kandelia candel）和桐花树（Aegiceras corniculatum）3种红树植物的新近落叶进行室内48 d分解实验,探讨了凋落叶分解过程对土壤可溶性有机碳（DOC）和可溶性总氮（TDN）含量、C/N比（DOC/TDN）及紫外-可见（UV-Vis）光谱特征（A280、A240/A420和A250/A365比值）的影响。在48 d分解期间,3种红树植物凋落叶的输入均明显增加了土壤DOC的含量,其变化在分解第6 d最为显著,各凋落叶添加组比对照组平均增加了149%（秋茄）~196%（桐花树）,随后各凋落叶添加组土壤DOC含量呈下降趋势。与土壤DOC的变化不同,凋落叶输入后土壤TDN的变化与对照组的差异不明显,但木榄和桐花树添加组的C/N比在分解初期（第6天）显著高于对照组（P<0.05）。凋落叶的输入亦在不同程度上增大了土壤DOM的A280值,降低了DOM的A240/A420和A250/A365比值。与土壤DOC的变化相似,凋落叶输入使DOM的UV-Vis光谱特征在分解初期（第6天）的变化最明显,其中桐花树凋落叶的影响最大,秋茄凋落叶的影响最小。结果表明：凋落叶输入使培养初期土壤DOM的含量和性质发生明显改变,DOM中大分子及芳香类组分增多、团聚化程度增加,DOM 的生物可降解性变小。然而,随着分解的进行,不同凋落叶处理组之间土壤DOM的变化差异性逐渐缩小,并在分解后期与对照组趋近。     

黑土有机质分解、积累及其变化规律

有机质是黑土肥力的基础,通过区域分析和长期定位试验探索有机质变化规律,结果表明,黑土有机质含量总体呈下降趋势,不同施肥处理对黑土有机质含量变化呈现不同变化趋势。     

设施土壤pH值与有机质演变特征研究

设施土壤的pH、有机质与土壤环境质量及设施栽培作物生产水平密切相关。文章对云南不同区域、不同大棚种植年限、不同轮作制度的设施土壤pH与有机质的演变特征进行研究,结果表明:大棚种植年限长的地区,土壤pH、有机质变化明显;随着大棚种植年限的增长,土壤pH呈下降趋势,有机质含量则呈上升趋势;随着土壤层次的加深,大棚土壤pH逐渐升高,而有机质则逐渐降低;不同轮作方式,花-菜轮作比菜-菜轮作有利于增加有机肥对设施土壤pH的缓冲性。