秦岭太白红杉林土壤有机碳密度研究

土壤有机碳(Soil Organic Carbon,SOC)库是陆地生态系统中最大的碳库,确定土壤有机碳储量及影响因子对碳循环和气候变化的研究具有重要意义.在秦岭太白山南、北坡分别沿不同海拔梯度共调查了太白红杉(Larix chinensis Beissn)林的18个样点,共计54个土壤剖面,分南、北坡对太白红杉林土壤有机碳密度进行了估算,并分析了土壤有机碳的主要影响因子.结果表明:太白红杉林北坡土壤有机碳平均密度在枯落物层为(0.31±0.18)kg/m2,在0～100 cm土层为(15.84±9.08)kg/m2;南坡土壤有机碳平均密度在枯落物层为(0.27±0.07)kg/m2,在0～100 cm土层为(14.51±7.85)kg/m2;太白红杉林南、北坡0～100 cm土层土壤有机碳平均密度为(15.18±8.51)kg/m2.秦岭太白红杉林北坡0～100 cm土层土壤有机碳密度随海拔的增加呈显著减小趋势(P0.05),此外,该层土壤有机碳密度随年降水量的增加呈下降趋势.土壤容重与w(有机碳)呈显著负相关(P0.05).     

长期施肥对棕壤有机碳储量及固碳速率的影响

利用棕壤肥料长期定位试验,研究了不同施肥条件下棕壤有机碳在0~60 cm土层的含量和储量特征以及土壤固碳速率.试验共设6个处理,即氮磷肥有机肥配施(M_2NP)、氮肥有机肥配施(M_2N)、单施有机肥(M_2)、单施氮肥(N)、氮磷肥配施(NP)和不施肥处理(CK).结果表明:经过31年长期不同施肥,各处理土壤有机碳(SOC)含量和储量的剖面分布均呈现随土层深度增加而显著降低的规律.本试验条件下M_2NP、M_2N、M_2、NP、N、CK处理的耕层有机碳富集系数分别为0.465、0.455、0.407、0.48_2、0.393、0.471,表明耕层土壤对有机碳的保持强度最强.在0~60 cm土层土壤有机碳储量表现为M_2NP、M_2NM_2、NPNCK,有机肥和化肥配施能够显著提高土壤有机碳含量和储量.与试验前相比,CK处理各土层土壤有机碳含量和储量均显著降低.各处理碳库管理指数(CPMI)表现为M_2NPM_2NM_2NNPCK.分析不同施肥处理土壤固碳速率可知,与试验前相比,CK处理表现为碳的净释放,固碳速率达-401.4 kg·hm~(-_2)·a~(-1);固碳速率最高的为M_2NP,M_2N,分别达到489kg·hm~(-_2)·a~(-1)、440._2 kg·hm~(-_2)·a~(-1).综合结果表明,化肥、有机肥配施所产生交互效应更有利于棕壤有机碳储量的增加及固碳速率的提高.     

垦殖对湿地土壤有机碳垂直分布及可溶性有机碳截留的影响

通过测定和计算兴凯湖地区沼泽湿地及由其垦殖而来的旱田和水田土壤剖面有机碳含量和密度及土壤剖面不同深度土壤溶液中可溶性有机碳含量,分析了垦殖对兴凯湖周边沼泽湿地土壤有机碳垂直分布及土壤剖面截留可溶性有机碳的影响.结果表明,垦殖显著影响湿地0～40 cm土壤有机碳含量,大豆田和水稻田0～10、10～20、20～30、30～40 cm土壤有机碳含量与湿地相比分别降低了79.07%和82.01%、79.01%和82.28%、79.86%和92.90%、37.49%和78.05%;40 cm以下土层土壤有机碳含量垦殖前后差异不显著.大豆田和水稻田有机碳密度相比沼泽湿地分别降低了25.50%和47.35%,但三者1 m深土壤中大部分的有机碳均是储存在0～50 cm土层中.垦殖前后土壤有机碳含量与深度之间的关系均可用指数函数来描述,垦殖改变了土壤有机碳含量但并未改变其随土壤深度的变化规律.垦殖为大豆田土壤剖面对可溶性有机碳的截留效果较湿地和水稻田更明显,沼泽湿地和水稻田对可溶性有机碳的截留效果大致相当.     

干旱沙区人工固沙植被演变过程中土壤有机碳氮储量及其分布特征

通过测定干旱沙区不同年代人工植被固沙区土壤剖面1 m深度容重和有机碳、全氮含量,估算了人工固沙植被演变过程中土壤有机碳和全氮储量特征及其垂直分布格局.研究表明,干旱沙区人工固沙植被演变过程中,0～100 cm深土壤有机碳和全氮储量均呈增加趋势;有机碳氮储量表现出了固沙初期的显著增加期(<16 a),随后的缓慢增加积累期(16～25 a),及后期的显著增加期(>25 a),该变化趋势主要体现在0～20 cm的表层.土壤有机碳氮储量增加程度随深度增加有降低趋势,并且表层土壤(0～20 cm)有机碳和全氮储量远大于深层土壤(20～100 cm);固沙初期土壤有机碳和全氮储量的增加体现在0～100 cm各个深度,而随后积累期主要体现在0～20 cm深度,固沙后期的增加也主要在0～20 cm深度,20 cm以下增加不明显;0～100 cm深土壤有机碳氮储量表聚性随固沙植被演变越来越明显.明确了降水<200 mm的沙区人工固沙过程中植被和土壤特征的改变对土壤有机碳氮储量及分布特征的影响,为更好地理解干旱人工植被区的碳循环特征和预测该生态系统与气候变化间的反馈关系奠定了基础.     

黄土塬区小流域深层土壤有机碳变化的影响因素

以黄土高原沟壑区王东沟小流域为对象,研究了地形(塬面、塬坡和沟道)、土地利用(自然草地、人工草地、人工林地、农地和果园)对0～200cm土层内土壤有机碳(soil organic carbon,SOC)垂直分布特征的影响,以揭示黄土高原小流域深层SOC储量及其影响因素.结果表明,SOC含量除表层(0～20cm)沟道(10.0g·kg-1)大于塬面(7.8g·kg-1)和塬坡(8.2g·kg-1)外,塬面底层SOC均显著高于塬坡和沟道;塬坡和沟道SOC含量随深度增加而降低,而塬面上呈现SOC随深度增加降低-升高-降低的变化趋势.塬面上,SOC含量呈现人工草地(5.4g·kg-1)农田(5.2g·kg-1)和果园(5.1g·kg-1)的趋势,影响深度为表层40cm;塬坡上,呈现自然草地(4.3g·kg-1)人工林地(3.8g·kg-1)人工草地(3.3g·kg-1)和果园(3.3g·kg-1)的趋势,影响深度达到100cm;而沟道内,林草地利用方式对整个垂直剖面分布的差异无显著影响.20～100cm土层SOC储量占0～100cm储量的67.6%;100～200cm土层SOC储量占0～200cm储量的37.3%,相当于0～100cm的63.8%.研究结果表明地形、土地利用显著(p0.05)影响SOC垂直分布特征;黄土高原沟壑区深层SOC储量巨大,不容忽视.     

赤峰市黄花甸子流域土壤有机碳含量的空间变异特征研究

选择内蒙古赤峰市敖汉旗黄花甸子流域为研究对象,运用地统计学和ArcGIS空间分析工具相结合的方法研究流域内土壤有机碳含量的空间变异特征以及土地利用方式对其的影响.结果表明,研究区0~10 cm土层范围有机碳含量具有中等空间相关关系,10~100 cm土层范围有机碳含量具有强烈空间相关关系,由随机性因素所引起的空间变异随土壤深度增加而降低.土地利用方式对土壤有机碳含量的影响随土壤深度的变化而发生改变,主要受植物根系分布特征的影响,各土层土壤有机碳平均含量由高到低表现为林地天然草地农地.     

种植花椒对喀斯特石漠化地区土壤有机碳矿化及活性有机碳的影响

以贵州西南部典型石漠化治理示范区内5年、17年、30年生花椒林和乔木林(约60年)土壤为对象,采用室内模拟培养方法研究了0~15、15~30、30~50 cm这3个剖面土壤有机碳的矿化特征及活性有机碳的含量变化.结果表明,30年生花椒林土壤有机碳累计矿化量在各层土壤中均高于对应的乔木林土壤,而5年、17年生花椒林地各层土壤则均低于对应的乔木林土壤,3种花椒林土壤有机碳累计矿化量分配比在各层均高于对应的乔木林土壤.长期种植花椒增加了土壤有机碳的矿化量,降低了土壤有机碳的稳定性.乔木林土壤易氧化有机碳和颗粒有机碳在各层均显著高于对应的3种花椒林土壤(P0.05).随花椒种植年限增加,土壤易氧化有机碳和颗粒有机碳含量在0~15 cm和15~30 cm土层先增加后减少,在30~50cm土层则为先减少后增加.短期花椒种植有利于土壤活性有机碳的增加,长期则降低了0~15 cm和15~30 cm层土壤活性有机碳含量,花椒种植有利于深层(30~50 cm)土壤活性有机碳的积累.     

尕海湿地植被退化过程中有机碳及相关土壤酶活性变化特征

以青藏高原东缘尕海湿地不同植被退化程度样地为研究对象,采用定位研究与室内试验相结合的方法,研究植被退化过程对土壤有机碳和土壤酶活性的影响。结果表明：植被退化显著影响土壤有机碳含量和土壤酶活性,降低了土壤有机碳的含量和酶促反应效率,且这种影响随土层深度变化有所不同。四种植被退化阶段有机碳含量和酶活性均值总体上（0~100 cm）表现为未退化>轻度退化>中度退化>重度退化。不同土层中,20~40 cm土层的有机碳含量中度退化>轻度退化;0~10 cm土层中淀粉酶和纤二糖酶中度退化阶段活性值较高;20~100 cm土层中蔗糖酶重度退化阶段活性值最高,纤二糖酶活性重度退化>中度退化。同一退化程度土壤有机碳含量、蔗糖酶和纤二糖酶活性随土层深度增加显著降低（P<0.05）;淀粉酶和纤维素酶活性在>40 cm土层中活性值有所上升,整体呈波动下降趋势。     

山东省土壤有机碳密度的空间分布特征及其影响因素

利用2010年完成的山东省多目标区域地球化学调查获得的双层网格化大密度、高精度土壤碳数据,估算了全省土壤表层(0～20 cm)、中上层(0～100 cm)和全层(0～160 cm)的土壤有机碳(SOC)密度及其储量,并分析不同土壤类型、地貌类型、土地利用类型下土壤有机碳密度及其储量的空间分布特征及影响因素. 结果表明:①山东省不同深度土壤碳库组成存在一定差异,其中表层土壤碳库以有机碳为主,而全层土壤碳库则以无机碳为主. ②全省表层土壤有机碳储量为350.65×106 t,平均土壤有机碳密度为2.22 kg/m2,但在不同土壤类型、地貌类型和土地利用类型之间差异显著. ③土壤中较高的w(黏粒)、w(Se)、w(TN)和稳定的C/N等土壤条件均可促使w(SOC)增加,而土壤盐渍化、高硅、富盐基离子的沙性土壤环境则不利于有机碳的积累;此外,人类活动对林地、草地的破坏,以及灌溉水田、园地、林地等土地利用方式的改变也会导致土壤有机碳流失;土壤有机碳积累受降水量影响明显,随多年平均降水量的增加而增大,但受气温影响不明显. 在各因素综合影响下,山东省表层土壤有机碳密度分布呈沿海低、鲁西北平原和胶莱盆地中等、鲁中南山地丘陵和中低山区偏高的分布特征.      

黑河中游边缘绿洲农田退耕还草的土壤碳、氮固存效应

研究黑河中游边缘绿洲农田退耕种植苜蓿5a后土壤碳、氮库的变化,通过对2个土类(开垦耕种的风沙土和灰棕漠土)退耕苜蓿地和相邻农田0～5、5～10和10～20cm土层土壤有机碳(SOC)和全氮(TN)、颗粒有机碳和氮(POC、PON)储量的分析表明:开垦耕种的风沙土和灰棕漠土有极低的SOC和TN含量,退耕种植苜蓿后0～20cm SOC储量提高了22.1%～27.8%,SOC的固存率平均为0.47 Mg/(hm²·a),0～5cm表层SOC储量变化最大,提高32%～66%;TN储量0～20cm储量变化不显著,在0～5cm表层TN储量风沙土和灰棕漠土分别提高12.8%和48.1%.退耕后POC和PON较SOC和TN有更显著的变化,其分配比例增加,0～20cm土层POC和PON储量分别提高22.8%～42.7%和18.6%～57.6%,在0～5cm变化最大;在瘠薄耕地转变为多年生苜蓿地后土壤C库的增加主要是由于POC的形成量增加.SOC含量相对更低的灰棕漠土比风沙土退耕后土壤C、N的增加更为明显.     

Toxic effects of acetochlor, methamidophos and their combination on nifH gene in soil

Toxic effects of two agrochemicals on nifH gene in agricultural black soil were investigated using denaturing gradient gel electrophoresis （DGGE） and sequencing approaches in a microcosm experiment. Changes of soil nifH gene diversity and composition were examined following the application of acetochlor, methamidophos and their combination. Acetochlor reduced the nifH gene diversity （both in gene richness and diversity index values） and caused changes in the nifH gene composition. The effects of acetochlor on nifH gene were strengthened as the concentration of acetochlor increased. Cluster analysis of DGGE banding patterns showed that nifH gene composition which had been affected by low concentration of acetochlor （50 mg/kg） recovered firstly. Methamidophos reduced nifH gene richness that except at 4 weeks. The medium concentration of methamidophos （150 mg/kg） caused the most apparent changes in nifH gene diversity at the first week while the high concentration of methamidophos （250 mg/kg） produced prominent effects on nifH gene diversity in the following weeks. Cluster analysis showed that minimal changes of nifH gene composition were found at 1 week and maximal changes at 4 weeks. Toxic effects of acetochlor and methamidophos combination on nifH gene were also apparent. Different nifH genes （bands） responded differently to the impact of agrochemicals： four individual bands were eliminated by the application of the agrochemicals, five bands became predominant by the stimulation of the agrochemicals, and four bands showed strong resistance to the influence of the agrochemicals. Fifteen prominent bands were partially sequenced, yielding 15 different nifH sequences, which were used for phylogenetic reconstructions. All sequences were affiliated with the alpha- and beta-proteobacteria, showing higher similarity to eight different diazotrophic genera.     

EDTA-enhanced phytoremediation of lead contaminated soil by Bidens maximowicziana

Phytoremediation is a potential cleanup technology for the removal of heavy metals from contaminated soils.Bidens maximowicziana is a new Pb hyperaccumulator,which not only has remarkable tolerance to Pb but also extraordinary accumulation capacity for Pb.The maximum Pb concentration was 1509.3 mg/kg in roots and 2164.7 mg/kg in overground tissues.The Pb distribution order in the B. maximowicziana was:leaf>stem>root.The effect of amendments on phytoremediation was also studied.The mobility of soil Pb and the Pb concentrations in plants were both increased by EDTA application.Compared with CK(control check),EDTA application promoted translocation of Pb to overground parts of the plant.The Pb concentrations in overground parts of plants was increased from 24.23-680.56 mg/kg to 29.07-1905.57 mg/kg.This research demonstrated that B.maximowicziana appeared to be suitable for phytoremediation of Pb contaminated soil,especially,combination with EDTA.     

Distribution and ecological effect of mercury in Laogang landfill, Shanghai, China

Laogang landfill near Shanghai is the largest landfill in China, and receives about 10000 t of daily garbage per day, Samples of topsoil and plants were analyzed to evaluate mercury pollution from the landfill. For topsoil samples, there were significant correlations among total mercury （HgT）, combinative mercury （Hgc） and gaseous mercury （HgG）, and content of total organic carbon （TOC）, but, no significantly relationship was found between Hg content and filling time. Hg content changes in vertical profiles with time showed that the average Hgv of profiles 1992, 1996, and 2000 was similar, but their average HgG was quite different. HgT was significantly correlated with Hgc in profile 1992 and 2000, and Hgv was significantly correlated with Hg6 in profile 1996. HgG/Hgv ratio in profile samples decreased in the order of （HgG,/HgT）1992〉（HgG/HgT）1996〉〉（HgG/HgT）2000. A simple outline of Hg release in landfill could be drawn： with increasing of filling time, degradation undergoes different biodegradation, accordingly, gaseous mercury goes through small, more, and small proportion to total mercury. Distribution of Hg in plants was inhomogeneous, following the order of leaf〉root〉stem. The highest value of leaf may be associated with higher atmospheric Hg from landfill. Ligneous plants （e.g. Phyllostachys glanca, Prunus salicina and Ligustrum lucidum） are capable of enriching more Hg than herbaceous plants.     

Arsenic uptake by arbuscular mycorrhizal maize （Zea mays L.） grown in an arsenic-contaminated soil with added phosphorus

The effects of arbuscular mycorrhizal (AM) fungus (Glomus mosseae) and phosphorus (P) addition (100 mg/kg soil) on arsenic (As) uptake by maize plants (Zea mays L.) from an As-contaminated soil were examined in a glasshouse experiment.Non-mycorrhizal and zero-P addition controls were included.Plant biomass and concentrations and uptake of As,P,and other nutrients,AM colonization,root lengths,and hyphal length densities were determined.The results indicated that addition of P significantly inhibited root colonization and development of extraradical mycelium.Root length and dry weight both increased markedly with mycorrhizal colonization under the zero-P treatments,but shoot and root biomass of AM plants was depressed by P application.AM fungal inoculation decreased shoot As concentrations when no P was added,and shoot and root As concentrations of AM plants increased 2.6 and 1.4 times with P addition,respectively.Shoot and root uptake of P,Mn,Cu,and Zn increased,but shoot Fe uptake decreased by 44.6%,with inoculation, when P was added.P addition reduced shoot P,Fe,Mn,Cu,and Zn uptake of AM plants,but increased root Fe and Mn uptake of the nonmycorrhizal ones.AM colonization therefore appeared to enhance plant tolerance to As in low P soil,and have some potential for the phytostabilization of As-contaminated soil,however,P application may introduce additional environmental risk by increasing soil As mobility.     

Enzymatic oxidation of aqueous pentachlorophenol

The influence of the nonionic surfactant Tween 80 on pentachlorophenol （PCP） oxidation catalyzed by horseradish peroxidase was studied. The surfactant was tested at concentrations below and above its critical micelle concentration （CMC）. Enhancement of PCP removal was observed at sub-CMCs. The presence of Tween 80 in the reaction mixture reduced enzyme inactivation which occurred through a combination of free radical attack and sorption by precipitated products. A simple first-order model was able to simulate time profiles for enzyme inactivation in the presence or absence of Tween 80. At supra-CMCs, the surfactant caused noticeable reductions in PCP removal, presumably through micelle partitioning of PCP which precluded the hydrophobic PCP molecule from interacting with the enzyme.     

Decomposition of alachlor by ozonation and its mechanism

Decomposition and corresponding mechanism of alachlor, an endocrine disruptor in water by ozonation were investigated. Results showed that alachlor could not be completely mineralized by ozone alone. Many intermediates and final products were formed during the process, including aromatic compounds, aliphatic carboxylic acids, and inorganic ions. In evoluting these products, some of them with weak polarity were qualitatively identified by GC-MS. The information of inorganic ions suggested that the dechlorination was the first and the fastest step in the ozonation of alachlor.     

Degradation of metabolites accumulated of benzo[a]pyrene by coupling Penicillium Chrysogenum with KMnO4

Several main metabolites of benzo[a]pyrene （BaP） formed by Penicillium chrysogenum, Benzo[a]pyrene-1,6-quinone （BP 1,6- quinone）, trans-7,8-dihydroxy-7,8-dihydrobenzo[a]pyrene （BP 7,8-diol）, 3-hydroxybenzo[a]pyrene （3-OHBP）, were identified by high-performance liquid chromatography （HPLC）. The three metabolites were liable to be accumulated and were hardly further metabolized because of their toxicity to microorganisms. However, their further degradation was essential for the complete degradation of BaP. To enhance their degradation, two methods, degradation by coupling Penicillium chrysogenum with KMnO4 and degradation only by Penicillium chrysogenum, were compared; Meanwhile, the parameters of degradation in the superior method were optimized. The results showed that （1） the method of coupling Penicillium chrysogenum with KMnO4 was better and was the first method to be used in the degradation of BaP and its metabolites; （2） the metabolite, BP 1,6-quinone was the most liable to be accumulated in pure cultures; （3） the effect of degradation was the best when the concentration of KMnO4 in the cultures was 0.01% （w/v）, concentration of the three compounds was 5 mg/L and pH was 6.2. Based on the experimental results, a novel concept with regard to the bioremediation of BaP-contaminated environment was discussed, considering the influence on environmental toxicity of the accumulated metabolites.     

Impact of atrazine and nitrogen fertilizers on the sorption of chlorotoluron in soil and model sorbents

Sorption of chlorotoluron in ammonium sulfate, urea and atrazine multi-solutes system was investigated by batch experiments. The results showed application of nitrogen fertilizers to the soil could affect the behavior of chlorotoluron. At the same concentration of N, sorption of chlorotoluron decreased as the concentration of atrazine increased on the day 0 and 6 in soil, respectively. The sorption of chlorotoluron increased from 0 to 6 d when soils were preincubated with deionized water, ammonium sulfate and urea solution for 6 d. That indicated incubation time was one of the most important factors for the sorption of chlorotoluron in nitrogen fertilizers treatments. The individual sorption isotherms of chlorotoluron in rubbery polymer and silica were strictly linear in single solute system, but there were competition sorption between pesticides or between pesticides and nitrogen fertilizers. That indicated the sorption taken place by concurrent solid-phase dissolution mechanism and sorption on the interface of water-organic matter or water-mineral matter.     

基于综合水质标识指数和对应分析法的校园河道水质评价

以三峡大学的校园河道求索溪为研究对象,利用综合水质标识指数法确定求索溪水质类别,分析其水质时空变化规律,并利用对应分析法得出求索溪中不同监测点的主要污染因子.研究结果表明:求索溪整体的综合水质标识指数为7.423,整体水质为劣V类(地表水环境质量标准GB 3838-2002)且黑臭.从时间变化来看,求索溪4月份的水质最差,5月份次之,4、5月份所有监测点的水质都劣于V类且黑臭;8月份水质最好,水质为Ⅳ类;从空间分布来看,8个监测点综合水质标识指数均超过6.0,水质为劣V类,其中6号监测点的水质相对最好,监测点3号的水质相对最差;对应分析法得出求索溪的整体水体污染程度受总氮因子的影响最大,其次为总磷.该研究拟为求索溪及类似校园河道的水环境治理研究提供基础依据和参考.     

Potential of plant polyphenol oxidases in the decolorization and removal of textile and non-textile dyes

In this study an effort has been made to use plant polyphenol oxidases; potato （Solanum tuberosum） and brinjal （Solanum melongena）, for the treatment of various important dyes used in textile and other industries. The ammonium sulphate fractionated enzyme preparations were used to treat a number of dyes under various experimental conditions. Majority of the treated dyes were maximally decolorized at pH 3.0. Some of the dyes were quickly decolorized whereas others were marginally decolorized. The initial first hour was sufficient for the maximum decolorization of dyes. The rate of decolorization was quite slow on long treatment of dyes. Enhancement in the dye decolorization was noticed on increasing the concentration of enzymes. The complex mixtures of dyes were treated with both preparations of polyphenol oxidases in the buffers of varying pH values. Potato polyphenol oxidase was significantly more effective in decolorizing the dyes to higher extent as compared to the enzyme obtained from brinjal polyphenol oxidase. Decolorization of dyes and their mixtures, followed by the formation of an insoluble precipitate, which could be easily removed simply by centrifugation.