长期不同施肥方式对江南稻田系统生产力与抗逆性的影响

依据29 a的田间施肥小区试验和4 a的养分耗竭盆栽试验,比较分析了不同施肥方式对江南丘陵稻田生产力及抗逆性的综合影响。结果表明,有机无机肥配施(NPK+OM处理)方式下,双季稻各季和周年生产力最高,其周年平均生物量和籽粒产量比化肥氮磷钾配施(NPK处理)高24.5%和20.2%。与单施氮肥相比,化肥氮磷钾配施显著提高了双季稻的氮素利用效率,而适量增施有机氮能够进一步提高氮素利用效率。化肥单施方式(N和NPK处理)下水稻周年籽粒产量呈递减趋势,下降幅度分别为43.7和1.8 kg.hm-2.a-1,而有机无机肥配施方式下水稻周年籽粒产量呈递增趋势,上升幅度为6.9 kg.hm-2.a-1。平衡施肥方式(NPK和NPK+OM处理)下,水稻各季及周年籽粒产量的年际变异较小,可持续性产量指数和系统生产力稳定性较高。养分耗竭试验4 a后,各处理水稻各季及周年生物量和籽粒产量高低基本表现为NPK+OM>NPK>N,试验期内周年籽粒平均产量以有机无机肥配施处理最高,说明有机无机肥配施的稻田土壤耐瘠能力高于其他施肥处理。可见,有机无机肥配施不仅能使稻田系统持续保持较高的生产力,而且能够提升系统的抗逆性,有利于江南丘陵稻田系...     

长江口海域表层沉积物污染及其潜在生态风险评价

根据2004年8月份长江口海域表层沉积物的监测基础资料,采用单因子污染参数法和Hakanson前在生态风险指数法,通过分析长江口不同水域表层沉积物中典型污染要素PCB,Hg,Cd,Pb,As的质量分数,评价了长江口表层沉积物的质量状况。定量确定了长江口表层沉积物的潜在生态风险程度、主要污染因子和潜在生态风险因子;分析了近年来长江口表层沉积物总的潜在生态风险和单个污染要素的潜在生态风险的变化趋势。结果表明:长江口表层沉积物质量状况良好,各典型污染要素的质量分数值均小于背景值,典型污染要素的平均综合指数Cd为1.37,典型污染要素的污染程度由高至低顺序为As>Pb>Hg>PCB>Cd,As是主要环境污染因子;长江口各水域表层沉积物总的对水域均只具有低潜在生态风险,其由高至低的排列顺序为杭州湾北岸>长江口南支>长江口北支>长江口外;各典型污染物对水域也均只具有低潜在生态风险,其由高至低顺序为Hg>PCB>Cd>As>Pb,Hg是主要潜在生态风险因子;近年来,长江口表层沉积物总的潜在生态风险和单个污染物的潜在生态风险均呈现增加趋势。     

夏季渭河西安段溶解性有机质(DOM)的特征、分布及来源分析

通过紫外吸收光谱,三维荧光光谱结合平行因子分析(EEMs-PARAFAC)方法及主成分分析(PCA),研究了夏季渭河西安段水体中的溶解性有机质(DOM)的组成、来源,及其与水质指标的相关性.在研究区域共检出2种类别5个不同的DOM组分,分别为类腐殖质荧光组分C1、C2、C3、C5和1个类蛋白类荧光组分C4,5个组分具有...     

基于水土流失的景观格局分析方法

景观格局和生态过程是景观生态学研究的重要内容,但是很多研究只重视景观格局的研究,而忽略了生态过程的研究。文章针对水土流失这一重要生态过程,提出了基于水土流失过程的景观坡度指数和景观空间负荷对比指数,并对黄土高原泾河流域15个子流域的景观格局进行了分析,认为泾河流北部各子流域主要以水土流失的＂源＂景观为主,景观坡度指数大,空间负荷指数小,水土流失风险大;流域南部各子流域上游以＂汇＂景观为主,坡度指数大,中下游以＂源＂景观为主,景观空间分布不均衡,存在一定的水土流失风险;流域东部局部子流域主要以水土流失的＂汇＂景观为主,＂源＂景观相对较小,＂源＂-＂汇＂景观空间分布均衡,水土流失风险小。     

珠江三角洲城市雨水的化学组成及其成因探讨

于2005—2007年间,基于降水过程监测分析了广州市和珠海市雨水的化学组成。结果表明,广州市雨水的pH值变化于3.32~7.03之间,平均值为4.35,众数约为4.15。珠海市雨水的pH值变化于3.38~6.49之间,平均值为4.51。雨水pH值随降水强度的减弱而降低,这决定于大气中水汽与酸性气体的接触时间。珠江三角洲城市雨水中所含主要离子依次是SO42-、NO3-、NH4＋、Ca2＋、Cl-。雨水的酸化与降水过程密切相关。降雨初期雨水比中后期雨水的pH值高,揭示降雨初期大气中的粉尘颗粒有效中和雨水的酸度。多天连续降水天气对大气尘埃的清洗作用明显,但是持续的SO2和NOx排放更容易使雨水酸化。滨海城市降水初期雨水的电导率上升较快（可以从小于1μS.cm-1上升到20~30μS.cm-1）,随着降水时间的延长雨水的电导率以较慢的速率上升。     

Effects of salinity on soil bacterial and archaeal community in estuarine wetlands and its implications for carbon sequestration: verification in the Yellow River Delta

Soils from two typical tidal salt marshes with varied salinity in the Yellow River Delta wetland were analysed to determine possible effects of salinity on soil carbon sequestration through changes in soil microbiology. The mean soil respiration (SR) of the salt water–fresh water mixing zone (MZ) was 2.89 times higher than that of the coastal zone (CZ) (4.73 and 1.63?μmol?m^?2?s^?1, respectively, p?Pseudomonas sp. and Limnobacter sp. that might have led to its higher dehydrogenase activity and respiratory rates. Additionally, the CZ possessed more Halobacteria and Thaumarchaeota with the ability to fix CO₂ than the MZ. Significantly lower soil salinity in MZ (4.25?g?kg^?1) was suitable for β-Proteobacteria, but detrimental for Halobacteria compared with CZ (7.09?g?kg^?1, p?相似文献   

纳米铁对沈阳细河水及周边村庄井水中重金属和溴的去除

在实验室条件下合成制得的纳米铁BET比表面积为49.16 m.2g-1,粒径范围为20—40 nm.通过批实验考察了纳米铁对沈阳细河河水和周边地下水中重金属及溴离子的去除效果.结果表明,纳米铁对水中Cr（Ⅵ）、Cu（Ⅱ）、Cd（Ⅱ）、Pb（Ⅱ）和As（Ⅲ）都有很好的去除效果,1.25 g.L-1纳米铁在30 min内,...     

Perfluorinated compounds in the Pearl River and Yangtze River of China

A total of 14 perfluorinated compounds (PFCs) were quantified in river water samples collected from tributaries of the Pearl River (Guangzhou Province, south China) and the Yangtze River (central China). Among the PFCs analyzed, perfluorooctane sulfonate (PFOS) and perfluorooctanoic acid (PFOA) were the two compounds with the highest concentrations. PFOS concentrations ranged from 0.90 to 99 ng/l and <0.01–14 ng/l in samples from the Pearl River and Yangtze River, respectively; whereas those for PFOA ranged from 0.85 to 13 ng/l and 2.0–260 ng/l. Lower concentrations were measured for perfluorobutane sulfonate (PFBS), perfluorohexane sulfonate (PFHxS), perfluorooctanesulfoamide (PFOSA), perfluorohexanoic acid (PFHxA), perfluoroheptanoic acid (PFHpA), perfluorononaoic acid (PFNA), perfluorodecanoic acid (PFDA), and perfluoroundecanoic acid (PFUnDA). Concentrations of several perfluorocarboxylic acids, including perfluorododecanoic acid (PFDoDA), perfluorotetradecanoic acid (PFTeDA), perfluorohexadecanoic acid (PFHxDA) and perfluorooctadecanoic acid (PFOcDA) were lower than the limits of quantification in all the samples analyzed. The highest concentrations of most PFCs were observed in water samples from the Yangtze River near Shanghai, the major industrial and financial centre in China. In addition, sampling locations in the lower reaches of the Yangtze River with a reduced flow rate might serve as a final sink for contaminants from the upstream river runoffs. Generally, PFOS was the dominant PFC found in samples from the Pearl River, while PFOA was the predominant PFC in water from the Yangtze River. Specifically, a considerable amount of PFBS (22.9–26.1% of total PFC analyzed) was measured in water collected near Nanjing, which indicates the presence of potential sources of PFBS in this part of China. Completely different PFC composition profiles were observed for samples from the Pearl River and the Yangtze River. This indicates the presence of dissimilar sources in these two regions.     

EU-wide survey of polar organic persistent pollutants in European river waters

This study provides the first EU-wide reconnaissance of the occurrence of polar organic persistent pollutants in European river waters. More than 100 individual water samples from over 100 European rivers from 27 European Countries were analysed for 35 selected compounds, comprising pharmaceuticals, pesticides, PFOS, PFOA, benzotriazoles, hormones, and endocrine disrupters. Around 40 laboratories participated in this sampling exercise. The most frequently and at the highest concentration levels detected compounds were benzotriazole, caffeine, carbamazepine, tolyltriazole, and nonylphenoxy acetic acid (NPE₁C). Only about 10% of the river water samples analysed could be classified as “very clean” in terms of chemical pollution. The rivers responsible for the major aqueous emissions of PFOS and PFOA from the European Continent could be identified. For the target compounds chosen, we are proposing “indicative warning levels” in surface waters, which are (for most compounds) close to the 90th percentile of all water samples analysed.