杭州西湖“香灰土”沉积物轻、重有机质组成特征及其环境意义

为探索城市浅水湖泊高有机质含量沉积物中有机质污染特征及其与氮、磷等营养元素的关系,调查了西湖8个湖区沉积物柱状样不同深度泥层有机质含量及其轻、重组分和氮磷污染特征,通过与国内相关湖泊有机质组分的比较,定量刻画了西湖"香灰土"沉积物的有机质特征.结果表明,西湖沉积物属典型高有机质含量底质,不同湖区底泥有机质含量平均值为28~251 g·kg-1;不同湖区沉积物有机质含量差别很大,引水入口湖区比其他湖区的有机质含量明显偏低;垂向上,大多湖区有机质含量随深度增加而增加,反映出有机质在西湖丰富的沉积历史.有机质轻/重组分离研究表明,西湖沉积物中轻组有机质含量为0.57~9.17 g·kg-1,平均占总有机质的2.83%,重组含量为5.35~347.41 g·kg-1,平均占总有机质的90%;与玄武湖、月湖、太湖、白洋淀等浅水湖泊相比,西湖底泥轻组有机质含量与之相当,但重组有机质含量明显偏高,反映出西湖作为历史悠久的城市湖泊,有机质污染负荷高,底泥腐殖化程度高.西湖底泥轻组有机质与总磷、总氮显著相关,而重组有机质含量仅与总氮含量显著相关,与磷没有相关性,表明轻组有机质对氮、磷内源释放潜力具有较大的影响.研究表明,西湖"香灰土"型沉积物有机质含量高、重组有机质比例高,对内源氮磷释放的缓冲能力强,在西湖营养盐内源负荷控制及水体富营养化治理中应予以充分考虑.     

Sorption of pyrene on two paddy soils and their particle-size fractions

In the present study, the sorption of pyrene on two kinds of bulk paddy soils, Gleyic Stagnic Anthrosols, and Ferric accumulic Stagnic Anthrosols as well as their particle-size fractions was investigated. The sorption isotherms fitted well with Freundlich equation. For both soils, the clay fraction（ 〈 2μm） and coarse sand fraction（2000-250μm） had higher sorption capacity than fine sand fraction（250-20 μm） and silt fraction（20-2 μm）. The IogKoc values obtained of each soil and its particle-size fractions were similar, proving that SOM content was a key factor affecting pyrene sorption. The Kd values showed a significant correlation with contents of dithionite-extractable Fe in both paddy soils and a good relationship with CEC in Gleyic Stagnic Anthrosols, indicating possible effects of surface properties of particle-size fractions on the sorption of pyrene.     

黑土真菌群落互作及其与梯度有机质碳分子结构的关系

真菌在土壤有机质积累、转化以及养分循环中发挥着重要功能.本文利用高通量ITS扩增子测序和固态~(13)C核磁共振波谱技术,比较低有机质(2%～5%)和高有机质(7%～9%)条件下,土壤真菌各类群间的互作关系及其与有机碳官能团结构的联系.~(13)C-NMR分析结果表明,O-Alkyl C占总有机碳的比例随着有机质含量的升高而增大(25.8%～35.9%).有机质含量越高,A/A-O(Alkyl C/O-Alkyl C)越小,有机质分解程度越低.真菌群落中粪壳菌纲(Sordariomycetes, 14.33%～28.17%)和被孢毛霉菌纲(Mortierellomycotina, 7.32%～23.14%)为优势类群,其相对丰度均随着土壤有机质含量的升高而显著增加(P0.05).网络分析结果表明,相比高有机质土壤,低有机质土壤中真菌生态网络的节点数、连接数和平均聚类系数较小,真菌互作关系更简单,且真菌与有机碳官能团联系更紧密,尤其与LOC联系更紧密.随机森林模型显示LOC对低有机质土壤真菌互作关系的解释量最高(10%),其次是难分解碳组分(ROC).相比LOC对高有机质土壤真菌互作关系的贡献相对较小(7.4%).在全球土壤碳损失日益严重的背景下,碳资源的限制,特别是LOC的减少,可能会降低土壤真菌群落的稳定性和多功能性.     

Cation exchange capacities of soil organic matter fractions in a Ferric Lixisol with different organic matter inputs

Soil organic matter (SOM) has an important effect on the physicochemical status of highly weathered soils in the tropics. This work was conducted to determine the contribution of different SOM fractions to the cation exchange capacity (CEC) of a tropical soil and to study the effect of organic matter inputs of different biochemical composition on the CEC of SOM. Soil samples were collected from a 20-year-old arboretum established on a Ferric Lixisol, under seven multipurpose tree species: Afzelia africana, Dactyladenia barteri, Gliricidia sepium, Gmelina arborea, Leucaena leucocephala, Pterocarpus santalinoides, and Treculia africana. Fractions were obtained by wet sieving and sedimentation after ultrasonic dispersion. Relationships between CEC and pH were determined using the silver thiourea-method and were described by linear regression. The CEC of the fractions smaller than 0.053 mm was inversely related to their particle size: clay (<0.002 mm)>fine silt (0.002–0.02 mm)>coarse silt (0.02–0.053 mm), except for the soils under T. africana, D. barteri, and L. leucocephala, where the CEC of the fine silt fraction was highest or comparable to the CEC of the clay fraction. The clay and fine silt fractions were responsible for 76–90% of the soil CEC at pH 5.8. The contribution of the fine silt fraction to the CEC at pH 5.8 ranged from 35 to 50%, which stressed the importance of the fine silt fraction for the physicochemical properties of the soil. Differences in CEC between treatments for the whole soil and the fractions could be explained by the differences in carbon content. Except for the intercept for the clay fraction, SOM had a significant (P<0.001) contribution to both the intercepts (=estimated CEC at pH 0) and slopes (=pH-dependent charge) of the CEC–pH relationships for the whole soil and the fractions. The CEC of SOM at pH 5.8 varied between 283 cmol_c kg⁻¹ C for particulate organic matter, and 563 cmol_c kg⁻¹ C for the fine silt fraction. The biochemical composition of the organic inputs did not have an important effect on the CEC of SOM. In total, SOM was responsible for 75–85% of the CEC of these soils.     

Effects of free iron oxyhydrates and soil organic matter on copper sorption-desorption behavior by size fractions of aggregates from two paddy soils

Effects of free iron oxyhydrates (Fed) and soil organic matter (SOM) on copper (Cu2+) sorption-desorption behavior by size fractions of aggregates from two typical paddy soils (Ferric-Accumulic Stagnic Anthrosol (Soil H) and Gleyic Stagnic Anthrosol (Soil W)) were investigated with and without treatment of dithionite-citrate-bicarbonate and of H2O2. The size fractions of aggregates were obtained from the undisturbed bulk topsoil using a low energy ultrasonic dispersion procedure. Experiments of equilibrium sorption and subsequent desorption were conducted at soil water ratio of 1:20, 25℃. For Soil H, Cu2+ sorption capacity of the DCB-treated size fractions was decreased by 5.9% for fine sand fraction, by 40.4% for coarse sand fraction, in comparison to 2.9% for the bulk sample. However, Cu2+ sorption capacities of the H2O2-treated fractions were decreased by over 80% for the coarse sand fraction and by 15% for the clay-sized fraction in comparison to 88% for bulk soil. For Soil W, Cu2+ sorption capacity of the DCB-treated size fraction was decreased by 30% for the coarse sand fraction and by over 75% for silt sand fraction in comparison to 44.5% for the bulk sample. Cu2+ sorption capacities of the H2O2-treated fractions were decreased by only 2.0% for the coarse sand fraction and by 15% for the fine sand fraction in comparison to by 3.4% for bulk soil. However, Cu2+ desorption rates were increased much in H2O2-treated samples by over 80% except the clay-sized fraction (only 9.5%) for Soil H. While removal of SOM with H2O2 tendend to increase desorption rate, DCB- and H2O2-treatments caused decrease in Cu2+ retention capacity of size fractions. Particularly, there hardly remained Cu2+ retention capacity by size fractions from Soil H after H2O2 treatment except for clay-sized fraction. These findings supported again the dominance of the coarse sand fraction in sorption of metals and the preference of absorbed metals bound to SOM in differently stabilized status among the size fractions. Thus, enrichment and turnover of SOM in paddy soils may have great effects on metal retention and chemical mobility in paddy soils.     

长期施肥措施下稻田土壤有机质稳定性研究

采用傅立叶变换红外光谱(FTIR)对典型稻田生态系统长期定位试验的土壤有机质(SOM)结构进行分析,探讨不同施肥处理下表层与深层土壤有机质的分布差异及其稳定性机制.结果表明,长期不同施肥措施下稻田表层土壤有机碳(SOC)含量以有机-无机肥配施处理最高,其中高量有机肥(HOM)、低量有机肥(LOM)和秸秆还田(STW)处理较对照(CK)处理分别增加了18.5%、12.9%和18.4%.土壤有机质的化学结构也存在一定的差异性,与CK相比,施肥处理均增加了土壤中化学抗性化合物(脂族性、芳香族)、碳水化合物以及有机硅化合物的官能团吸收强度,其中HOM、LOM和STW处理最为明显.以烷烃类化合物为例,HOM、LOM和STW处理下其吸收强度为0.30、0.25和0.29,较CK分别增加了87%、56%和81%.表层土壤有机质各官能团的吸收峰强度皆高于深层土壤,同样以HOM、LOM和STW处理的差异最显著.本研究结果揭示了长期有机-无机肥配施下对亚热带稻田土壤有机质较丰富的化学抗性官能团结构的影响,贡献于其较高的有机质含量,这也从一方面揭示了稻田土壤有机质积累的化学稳定机制.     

重庆渝北地区土壤重金属形态特征及其有效性评价

结合渝北地区土壤重金属全量及形态分析,对区内主要土壤类型(紫色土、石灰土、黄壤、水稻土)中的As、Cd、Cr、Pb形态构成特征、影响因素及有效性进行研究. 结果表明:不同土壤类型重金属形态构成差异明显,Cr、Pb在各土壤类型中均以残渣态为主;Cd在黄壤、紫色土中以离子态、残渣态为主,其中离子态平均构成在2类土中分别高达37.44%、29.97%. w(可利用态As)和w(可利用态Cr)在紫色土中的平均值分别为0.04和0.96mg/kg,w(可利用态Cd)在水稻土和紫色土中的平均值分别为0.13和0.09mg/kg,w(可利用态Pb)在黄壤中的平均值为1.94mg/kg,表现出较高生物有效性;石灰土中各重金属可利用态总体较低. w(可利用态As)、w(可利用态Cd)分别与As全量(以w计,下同)、Cd全量呈显著正相关;w(可利用态Cd)和w(可利用态Pb)与pH,w(可利用态Cr)与w(有机质)均呈显著负相关. 紫色土中w(可利用态Cd)、w(可利用态Cr)和w(可利用态Pb)与各重金属全量、pH和w(有机质)三者显著服从多元非线性对数回归,通过该回归可对研究区紫色土这3个元素的可利用态含量进行预测.      

典型黑色岩系地质高背景区土壤和农产品重金属富集特征与污染风险

土壤重金属污染是我国的重要环境问题,而区域地质高背景是土壤重金属富集的重要影响因素.黑色岩系风化土壤普遍存在重金属富集的现象,潜在生态环境风险较高,但目前农产品重金属富集的基础数据较缺乏,限制了黑色岩系地质高背景区的土地安全利用与农产品安全生产.对重庆典型黑色岩系地质高背景区313件土壤和289件主要农产品重金属的富集特征、污染风险和土壤重金属赋存形态进行研究.结果表明,相对于我国土壤环境背景值和重庆市表层土壤,研究区土壤Cd、 Cr、 Cu、 Zn和Se富集,Pb不富集;其中98.7%的土壤Cd含量超过风险筛选值,47.3%的土壤Cd含量超过风险管制值,Cd的污染水平和潜在生态风险最高,是研究区土壤的特征污染物.土壤Cd主要以离子交换态存在(40.6%),其次为残渣态(19.1%)和弱有机结合态(16.6%); Cr、 Cu、 Pb、 Se和Zn主要以残渣态存在,Se和Cu的有机结合态、 Pb的铁锰结合态也占较高比例;说明Cd的迁移能力和活性高于其它重金属.研究区主要农产品富集重金属的能力较弱,约18.7%的农产品Cd超标,超标倍数相对较低,重金属污染风险较低.研究可为黑色岩系地质高...     

北京市不同区位耕作土壤中重金属总量与形态分布特征

采集北京市不同区位(中心城区、近郊平原、远郊平原)的代表性耕作土壤-麦粒匹配样品23组,分析不同人类活动强度影响下耕作土壤中重金属(Cd、Cu、Zn、Pb)全量、赋存形态以及生物有效性,并探讨其来源差异与健康风险.结果表明:①频繁的交通活动与工业释放致使中心城区(Pb平均含量为35.59 mg·kg-1)土壤呈现出较为明显的Pb富集特征,而长期污水灌溉等农业活动导致了近郊平原局部土壤重金属的明显积累.②土壤中Cu、Zn和Pb主要以残余态(35%～75%)与有机结合态(23%～53%)形式存在,其次是铁锰氧化态(1%～19%),而碳酸盐结合态(n.d.～5%)与离子交换态(n.d.～2%)含量非常少.Pb、Zn和Cu的生物可利用性从中心城区到近郊平原、远郊平原逐渐下降,Cd则呈相反的趋势.近远郊土壤中Cd的离子交换态(13%～31%)与碳酸盐结合态(11%～27%)占有相当高的比例,在4种重金属中生物可利用性最高.③Cd与Zn在麦粒中的含量与土壤中金属的铁锰氧化态含量正相关(P<0.05,r为0.43～0.57);④种植于中心城区与近郊土壤上的小麦籽粒中部分Zn、Pb含量超出了WHO限值,对当地居民健康构成潜在风险.     

芘在土壤中的长期吸附和解吸行为

研究了芘在6种不同性质土壤中长期吸附解吸及不可逆吸附行为.实验结果表明:长期实验中芘在土壤中的吸附和解吸都存在快过程和慢过程2个阶段.不同吸附平衡时间下,有机质含量高于1%时,不同土壤的吸附平衡常数随有机质含量的增加而增加;有机质含量低于1%时,黏粒含量对土壤的吸附能力有着重要影响;平衡时间由2d增加到180d后,6种土壤的Kd值增加了35.1%～557.9%,其中土壤有机质对Kd值有不同程度的影响,而黏粒对Ka值影响最大,平衡时间对部分土壤Kd值影响不容忽视.长期解吸过程中,6种土壤慢解吸部分占总解吸量的12.05%～41.00%,有机质含量越高,慢解吸对解吸过程的贡献越大.不考虑老化的影响,有机质含量对不可逆吸附容量的贡献明显高于黏粒的贡献,与有机质对慢解吸过程的影响有一致性.     

应用过硫酸盐氧化法预测焦化厂土壤中PAHs的生物有效性

采用过硫酸盐氧化法测定了北京市某焦化厂表层土壤中16种PAHs的生物有效性,并分析了过硫酸盐氧化前、后SOM(土壤有机质)的质量分数及其结构组成,以研究过硫酸盐氧化法预测焦化厂土壤中PAHs生物有效性方面的可行性. 结果表明:①7个供试土壤样品中w(∑PAHs)(16种PAHs质量分数之和)为10.80~249.00 mg/kg,并以HPAHs(高分子量PAHs)为主,不同环数PAHs的质量分数与w(SOM)均呈正相关,二者关系符合对数方程(R2为0.653~0.798). ②依据过硫酸盐氧化前、后土壤中w(PAHs)的变化得到PAHs的生物有效性,其中,2~3环PAHs的生物有效性平均值为0.46,略高于4环PAHs(0.22)和5~6环PAHs(0.28),较高w(SOM)及HPAHs均易引起焦化厂土壤中PAHs生物有效性的下降. ③过硫酸盐氧化前不同环数PAHs的质量分数与氧化后PAHs的残留量呈显著正相关(R2为0.991~0.994),故可利用过硫酸盐氧化前的w(PAHs)预测土壤中PAHs的生物有效性. ④与过硫酸盐氧化前相比,氧化后土壤中w(SOM)平均下降23.0%,FTIR(傅里叶变换红外光谱)分析结果显示,1 448 cm-1处吸收峰表征的脂肪碳可能是被氧化去除的软质碳的主要组分,氧化后SOM中的芳香碳相对吸光度增幅为0.88%~11.62%,可引起SOM的缩合程度加剧、憎水性增强. 因此,过硫酸盐氧化法能够作为测定焦化厂土壤中PAHs生物有效性的快速方法,可利用过硫酸盐氧化前的w(PAHs)预测土壤中PAHs的生物有效性.      

土壤中多环芳烃的SPMD辅助解吸行为研究

为了开发一种表征土壤中憎水性有机污染物解吸及生物有效性的新方法,建立了半透膜被动采样装置（SPMD）研究土壤中有机污染物解吸行为的方法,利用SPMD分析了多环芳烃菲、芘和苯并［a］芘在3种不同性质土壤中的辅助解吸行为.结果表明,SPMD是一种很好地表征土壤中憎水性有机污染物解吸及生物有效性的手段. SPMD辅助解吸多环芳烃的效率与土壤有机质及多环芳烃性质有关.随着土壤有机质含量的降低,土壤中菲和芘的SPMD解吸率逐渐升高,对于10 mg/kg染毒水平,当土壤有机质含量由18.68%降低到0.3%时,2种化合物的解吸率分别由56.45%和48.28%上升到接近100%;但是对于苯并［a］芘,粘土表现出明显的滞留能力,在有机质含量（0.3%）很低、粘土含量（39.05%）较高的3号土壤中,苯并［a］芘的解吸率仅有66.97%.不同多环芳烃SPMD辅助解吸率差别很大,随着土壤有机质含量的降低,以及污染物浓度的提高,菲和芘的解吸差异逐渐缩小,而苯并［a］芘与上述2种多环芳烃的差异很大,主要是由于苯并［a］芘具有高度亲脂性,并且分子较大,造成其容易滞留在粘土的微孔及有机质的致密结构中.     

The role of soil organic matter in maintaining the productivity and yield stability of cereals in China

The role of soil organic matter (SOM) in agricultural systems has been widely studied in conjunction with the potential for greenhouse gas mitigation. However, the link between SOM accumulation in croplands, crop productivity and yield stability has not yet been clearly established. In this paper, we collected data on provincial yearly crop productivity (yields, total cropland area) during 1949–1998 and the average SOM contents in croplands sampled and determined from the National Soil Survey in 1979–1982 of mainland China. The cereal productivity was assessed both with an overall mean of 1949–1998 and with the mean values for different time periods within this overall time, respectively. The yield variability within a single stabilizing stage, and between the fluctuating years, was calculated as a negative measure of yield stability. The correlation between SOM and cereal productivity was very significant for most provinces, but the relationship has become less significant as we approach the present. Moreover, the average yield variability was very significantly and negatively correlated with the cropland SOM level. The findings support our previous hypothesis from case studies, that C sequestration in China's croplands may provide win–win benefits, by enhancing crop productivity and stabilizing yield. This offers a sound basis as a greenhouse gas mitigation strategy by promoting C sequestration in croplands, and enhancing food security in China's agriculture.     

外加芘在2种水稻土及其团聚体培养中的老化及其可浸提性和生物有效性的变化

老化是指有机污染物进入土壤后,随着时间的增加,其生物有效性、毒性和可浸提性会逐渐下降的现象.采用室内培养法研究了外加多环芳烃芘在2种水稻土乌栅土(潜育型水稻土)和黄泥土(潴育型水稻土)及其不同粒组团聚体中的老化现象,并采用二氯甲烷提取和蚯蚓吸收试验比较了培养老化后外加多环芳烃芘的可浸提性和生物有效性的变化.结果表明,培养90d后芘的浸提率下降了15%~23%,蚯蚓的摄食量也下降了37%~67%,说明外加有机污染物进入水稻土后发生了显著的老化现象,从而降低了其环境移动性和生物有效性.但不同粒径团聚体中老化程度没有差异,不过对蚯蚓的生物有效性存在差异.因此,并不能根据土壤中有机污染物的含量来预测其环境风险和生物有效性.     

不同水分条件沼泽湿地土壤轻组有机碳与微生物活性动态

通过野外实验与室内分析,对三江平原生长季内毛果苔草(Carex lasiocapa)沼泽湿地生物量及0~20cm土壤不同有机碳组分进行观测,分析了不同水分条件下毛果苔草湿地土壤轻组有机碳(LFOC)与微生物量碳(MBC)的变化动态.结果表明,随水位增加毛果苔草群落地上生物量积累明显,与10~20cm积水条件相比,17~30cm水位状况下湿地土壤具有较高的轻组有机质含量与比例.生长季初期冻融过程提高了土壤轻组分(LF)有机碳含量与LFOC含量,之后随植物生长毛果苔草沼泽湿地土壤重组有机碳(HFOC)含量增长快于LFOC,说明毛果苔草沼泽湿地土壤具有较高的重组有机质持有能力.此外不同水位条件下毛果苔草沼泽湿地微生物活性受到土壤有机碳含量影响不同,低水位条件下微生物量碳与SOC呈显著正相关关系(R2=0.859),17~30cm水位条件下二者关系不显著,并且高水位毛果苔草沼泽湿地具有较低的MBC与微生物熵,表明该条件下土壤碳库具有较高的稳定性.     

Distribution of Cu and Pb in particle size fractions of urban soils from different city zones of Nanjing, China

Soil samples from 4 defined city zones of Nanjing were randomly collected at 0-5 cm and 5-20 cm intervals and size fractions of soil particles were separated from undisturbed bulk soils by low energy dispersion procedure. The total contents of Cu and Pb in the different particle size fractions of the urban soils were analyzed by HNO3-HF-HClO4 digestion and flame atomic absorption spectrophotometer determination. The total content of Cu and Pb in soil particle size fractions varied with their size and with city zones as well. Both the content and variation with the size fractions of Pb was bigger than of Cu supporting our previous finding that there was Pb pollution to different degrees in the urban soils although the two elements were generally enriched in clay-sized fraction. Contaminated Pb tended to be preferentially enriched in the size fraction of 2000-250 μm and clay-sized fraction. While the size fractions of the soils from newly developed and preserved area contained smaller amount of Cu and Pb, the partitioning of them in coarse and fine particle size fractions were insignificant compared to that from inner residence and commercial area. The very high Pb level over 150 mg/kg of the fine particle fractions from the soils of the inner city could be a cause of high blood Pb level reported of children from the city as acute exposure to Pb of fine particles of the urban soil might occur by soil ingestion and inhalation by young children. Thus, much attention should be paid to the partitioning of toxic metals in fine soil particles of the urban soils and countermeasures against high health risk of Pb exposure by soil ingestion and dust inhalation should be practiced against the health problem of blood Pb for young children from the cities.     

典型碳酸盐岩区耕地土壤剖面重金属形态迁移转化特征及生态风险评价

碳酸盐岩土壤母质区是我国耕地土壤重金属高含量的主要分布区,且耕地重金属迁移转化受到自然过程与人为活动的交互影响.以广西碳酸盐岩母质水田9条土壤剖面为研究对象,在分析测试土壤Cd、As、Zn、Cr、Cu、Hg、Ni和Pb含量、pH、Corg含量等土壤性质指标以及Cd、As、Zn和Cr赋存形态基础上,重点探讨了研究区耕地土壤重金属形态垂向分布特征、重金属生态风险以及对比在自然成土过程中和人为活动干扰下重金属迁移转化的影响因素.结果表明,研究区土壤剖面中Cd、As、Zn和Cr存在样本超农用地（水田）污染风险筛选值,Cd和As部分超管制值.土壤剖面Cd各形态均有一定比例分布,且随剖面深度由浅至深,Cd生态风险较高的水溶态、离子交换态比例呈显著下降趋势;土壤剖面As、Zn和Cr各深度段均以残渣态为主,随深度加深,水溶态和离子交换态比例变化不大.风险评价编码法（RAC）和次生相与原生相分布比值法（RSP）评价结果显示,研究区土壤Cd污染风险相对较高,总体上As、Zn和Cr处于无污染或无风险状态.研究区自然发育的土壤,黏土矿物含量和土壤发育程度对Cd迁移活动性的影响较为显著,而受人为活动影响的耕作层中,土壤pH与有机质含量则成为其迁移活动性的主控因素;土壤As的迁移能力主要与土壤有机质、Fe₂O₃含量以及土壤发育程度有关,但在耕作层中,有机质对其控制作用明显增强;土壤中Zn、Cr迁移能力的主控因素均为pH,而在人类活动干扰下,pH对其影响更为强烈.     

轻组有机质对太湖沉积物氮、磷矿化的影响

采用连续淹水培养试验研究轻组有机质(LFOM)对鼋头渚(Y)和贡湖(G)2种不同污染程度太湖沉积物氮、磷矿化的影响. 结果表明,去除LFOM并没有改变沉积物氮、磷的矿化趋势. 试验初期,沉积物累积矿化氮、磷量急速上升,之后增速变慢,至峰值后迅速下降,42 d时达到最小值,并持续至试验结束. 经过77 d的培养试验,不同处理的2种不同污染程度沉积物有24%～39%的总氮(TN)和7%～26%的总磷(TP)被矿化;污染较重的沉积物Y的净矿化氮、磷量和矿化速率均高于沉积物G;去除LFOM使沉积物的净矿化氮、磷量和矿化速率均有所降低,其中沉积物Y的净矿化氮、磷量分别降低了110.86和145.26 mg/kg,下降了15%和74%,沉积物G降低了195.13和29.99 mg/kg,下降了40%和50%. 沉积物Y的氮、磷平均矿化速率分别降低了3.01和5.36 mg/(kg·d),沉积物G分别降低了6.35和1.30 mg/(kg·d).      

A comparison of the compositional differences between humic fractions isolated by the IHSS and exhaustive extraction procedures

Humic substances (HSs), consisting, on the basis of solubilities in aqueous acid and basic media, of humic acids (HAs), fulvic acids (FAs), and humin (Hu), are the major components of soil organic matter (SOM). Most studies of soil/natural organic matter (SOM/NOM) have been carried out on extracts of soils in dilute sodium hydroxide solutions, the solvent used to extract the Standards of the International Humic Substances Society (IHSS). However, Hu, the major component in the classical definition of HSs, is insoluble in aqueous base and is not isolated by the traditional IHSS method. Recently, a sequential exhaustive extraction (SEE) process has been shown to be capable of isolating and separating the major components of the classically defined HSs from the soils of the temperate and tropical regions. The SEE system was used in the present study to isolate the HA/FA and Hu fractions from a subtropical volcanic Taiwanese soil. Chemical and compositional properties of these extracts were then compared with similarly obtained isolates from soils from the different climatic regions. Increases in the aliphatic relative to aromatic carbon contents were observed for both the HA and FA fractions when the pH values of the extraction media were increased. HAs and FAs isolated using the SEE method have spectroscopic profiles similar to those from the IHSS isolate; however, the cumulative extraction efficiency (%) of the SEE method (65 %) for the volcanic soil was much higher than for the traditional IHSS method (33 %). When the residual volcanic soil, following extractions once, three, and eight times with 0.1 M NaOH were then extracted with dimethyl sulphoxide (DMSO) plus concentrated sulphuric acid (the final solvent in the SEE sequence) it was seen that the content of crystalline polymethylene hydrocarbon (33 ppm ¹³C-NMR resonance in the Hu (or DMSO/acid)) extract increased relative to the amorphous methylene (30 ppm). That highlights the difficulty in dissolving the more highly ordered hydrocarbon structures that would be expected to have closer associations with the mineral colloids. Although the SEE procedure isolated all of the HAs and FAs from the Yangmingshan soil, extractability of the Hu from the volcanic soil in the DMSO/acid solvent was low (21 %), and contrasted with the much higher yields from temperate and tropical regions. The decreased Hu extraction may arise from its associations with the extensive iron and aluminium hydroxide mineral colloids in the soil. The Hu from this sub-tropical soil was different from the Hus isolated from other soil types, indicating the need to isolate and characterise these recalcitrant organic material in order to understand the organic carbon components in soils in greater detail. Such results would indicate that more attention should be given to mineral colloids in soils, and to the organo/mineral associations that will have an important role in the stabilities of OM in the soil environment.     

Effects of two sludge application on fractionation and phytotoxicity of zinc and copper in soil

The potential harm of heavy metals is a primary concern in application of sludge to the agricultural land.A pot experiment was conducted to evaluate the effect of two sludges on fractionation of Zn and Cu in soil and their phytotoxicity to pakchoi.The loamy soil was mixed with 0%,20%,40%,60% and 80%(by weight)of digested sewage sludge(SS)and composted sludge (SC).The additions of the both sludges caused a significant raise in all fractions,resulting in that exchangeable(EXCH)and organic matter(OM) became predominance for Zn and organic bound Cu occupied the largest portion.There was more available amount for Zn and Cu in SS treatments than SC treatments.During the pot experiment,the concentration of Zn in EXCH,carbonate(CAR)and OM and Cu in EXCH and OM fractions decreased in all treatments,so their bioavailability reduced.Germination rate and plant biomass decreased when the addition rate was high and the best yield appeared in 20% mixtures at the harvest of pakchoi.The two sludges increased tissue contents of Zn and Cu especially in the SS treatments.Zn in pakchoi was not only in relationship toΔEXCH andΔCAR forms but also inΔOM forms in the sludge-soil mixtures.Tissue content of Cu in pakchoi grown on SC-soils could not be predicted byΔEXCH. These correlation rates between Zn and Cu accumulation in pakchoi and variation of different fractions increased with time,which might indicate that sludges represented stronger impacts on the plant in long-term land application.