湿地生态系统硅生物地球化学循环研究进展

硅在地壳中的丰度仅次于氧,是地球表面大多数土壤和岩石的一种基本成分,也是水生植物（特别是硅藻类）以及多种作物生长所必需的营养元素,还是控制陆地、海洋、沿海和内陆水生态系统机能的重要营养元素。目前关于全球硅的生物地球化学循环的研究多集中在陆地和海洋两大生态系统,而湿地生态系统中硅的循环过程、储存量尚不清楚。虽然在河口湿地开展一些关于硅的相关研究,但是硅在湿地的循环机制研究不够全面,尤其相比碳、氮、磷等元素,硅素研究甚少。而且,国内关于硅的相关研究更为匮乏。本文在总结国内外关于湿地生态系统硅素研究的基础上,综述硅在湿地生态系统的存在形态与分布特征,阐述硅在湿地生态系统中的基本循环过程,列举影响硅在湿地生态系统中循环的主要因素,如：湿地类型、水淹时间、季节变化、人类干扰等;提出在今后研究工作中应进一步探索硅在湿地生态系统中迁移、转化的机制,加深研究人类活动对湿地生态系统硅循环的影响,特别是应该加强研究河口潮汐湿地和沿海湿地生态系统硅的生物地球化学循环过程和储存量,有助于明确湿地生态系统对于硅的截留量;并弄清湿地中碳与硅含量之间的关系,从水文学角度分析湿地中排水、蒸发、洪期及滞留时间等因素对硅循环的影响,从而试图建立湿地硅循环模型,有助于预测湿地生态系统硅循环对沿海地区赤潮等富营养化现象和全球气候变化的影响。     

Validation of polymer-based nano-iron oxide in further phosphorus removal from bioeffluent: laboratory and scaledup study

The efficient removal of phosphorous from water is an important but challenging task. In this study, we validated the applicability of a new commercially available nanocomposite adsorbent, i.e., a polymer-based hydrated ferric oxide nanocomposite (HFO-201), for the further removal of phosphorous from the bioeffluent discharged from a municipal wastewater treatment plant, and the operating parameters such as the flow rate, temperature and composition of the regenerants were optimized. Laboratory-scale results indicate that phosphorous in real bioeffluent can be effectively removed from 0.92 mg·L^-1 to<0.5 mg·L^-1 (or even<0.1 mg·L^-1 as desired) by the new adsorbent at a flow rate of 50 bed volume (BV) per hour and treatable volume of 3500–4000 BV per run. Phosphorous removal is independent of the ambient temperature in the range of 15°C–40°C. Moreover, the exhausted HFO-201 can be regenerated by a 2% NaOH+ 5% NaCl binary solution for repeated use without significant capacity loss. A scaled-up study further indicated that even though the initial total phosphorus (TP) was as high as 2 mg·L^-1, it could be reduced to<0.5 mg·L^-1, with a working capacity of 4.4–4.8 g·L^-1 HFO-201. In general, HFO-201 adsorption is a choice method for the efficient removal of phosphate from biotreated waste effluent.     

羟基化多溴联苯醚(OH-PBDEs)在小鼠肝脏微粒体的体外代谢及对CYP450酶活性的影响

羟基化多溴联苯醚(OH-PBDEs)是一类具有内分泌干扰效应的酚类化合物,生物毒性要高于母体多溴联苯醚(PBDEs),研究OH-PBDEs的体外代谢行为对于理解其在生物体内的富集转化具有重要意义。以小鼠肝脏微粒体作为研究对象,考察了3-OH-BDE-47、5-OH-BDE-47、6-OH-BDE-47和2’-OH-BDE-68在小鼠肝脏中的体外代谢,并分别研究了浓度为0.1、0.2、0.4、0.6、1.0μmol·L-1条件下4种OH-PBDEs对细胞色素P450酶系中7-乙氧基香豆素-O-脱乙基酶(ECOD)、7-乙氧基异吩唑酮-O-脱乙基酶(EROD)和苯胺4-羟基化酶(ANH)活性的影响。结果表明,4种OH-PBDEs在小鼠肝脏微粒体中均能够快速代谢,代谢率分别为80%(3-OH-BDE-47)、42%(5-OH-BDE-47)、86%(6-OH-BDE-47)和63%(2’-OH-BDE-68)。实验所设OH-PBDEs各浓度对微粒体的ECOD活性无显著性抑制作用,但对EROD的活性均表现出相同的显著抑制作用;4种OH-PBDEs表现出不同的ANH活性影响,即3-OH-BDE-47对ANH活性具有抑制作用,5-OH-BDE-47具有诱导作用,而6-OH-BDE-47和2’-OH-BDE-68对ANH活性无显著性影响。     

短期酸化对新安江流域屯溪段水体浮游植物群落结构及多样性的影响

为了探讨酸雨引起的水体酸化对新安江流域屯溪段浮游植物群落结构、丰度以及多样性的影响,对该流域3个采样站点以及流域附近一小型人工湖泊内浮游植物(同源性不同)进行调查并模拟酸胁迫(p H值4.50、5.65)处理。经酸化处理24 h后,各采样站点浮游植物与未经模拟酸雨处理的对照组相比种类及丰度呈降低趋势;较低p H值下(4.50)金藻门、黄藻门种类消失,优势种类硅藻门和绿藻门浮游植物受到的影响较大,种属数降低范围为0%~75%和27.3%~79.2%,蓝藻门受影响较小,裸藻门、甲藻门种属数未受影响;整体上各站点辛普森多样性指数、香农-维纳指数经酸化处理后均呈降低趋势。水体酸化对浮游植物种类与丰度的抑制效应在高NH3-N和总磷水平下较小。研究结果表明,不同门类浮游植物对酸胁迫的敏感性有较大差异,群落组成不同的水体,短期酸化处理都会显著改变浮游植物群落结构、降低浮游植物丰度以及多样性。作为长期受酸雨胁迫较为严重的地区,酸雨引起的水体酸化将可能成为影响新安江流域浮游植物群落结构的重要因子。     

玉米赤霉烯酮暴露导致的秀丽隐杆线虫生殖及发育毒性的世代间比较

利用模式生物秀丽隐杆线虫(Caenorhabditis elegans,C.elegans)对玉米赤霉烯酮(zearalenone,ZEN)暴露导致的生殖、发育缺陷在世代间的可传递性进行了研究。对亲代染毒,后代断毒恢复,实验结果显示,ZEN暴露导致的体长发育缺陷可在线虫后代中得到恢复,而生殖毒性可产生严重缺陷,且这种缺陷在后代中没有明显的恢复。通过多代持续染毒实验,发现ZEN对亲代P0、子一代F1和子二代F2线虫产生的生殖和发育毒性存在差异,其毒性作用强度为P0F2F1。线虫世代之间的发育缺陷和生殖缺陷表现出逐代修复的规律,但修复程度不同,推测与线虫自身修复的复杂应激活动有关。     

菲在土壤中的微生物降解研究

研究了不同条件土壤中多环芳烃菲的降解动态。结果表明：温度和底物浓度对土壤中菲的降解有较大影响,未灭菌土壤中菲的降解半衰期为5.1d;从污染土壤中分离到一株高效降解菲的菌株,经16S rDNA鉴定为产碱杆菌属（Alcaligenes bacterium LBM.）,同源性高达99%;随着优势菌接种量增加,基础培养基中菲降解速率逐渐加快;Fe3＋、Co2＋和Cu2＋对优势菌降解菲能力均有不同程度影响,其中以Fe3＋影响最明显。     

Dissipation and residues determination of propamocarb in ginseng and soil by high-performance liquid chromatography coupled with tandem mass spectrometry

Two-year field trials were performed at two experimental sites to investigate dissipation and terminal residues of propamocarb in ginseng root, stem, leaf, and soil by high-performance liquid chromatography coupled with tandem mass spectrometry (HPLC-MS/MS). Mean recoveries ranged from 80.5 to 95.6 % with relative standard deviations (RSDs) of 5.5–9.1 % at fortified levels of 0.01, 0.02, 0.05 and 0.20 mg kg^?1. The half-lives of propamocarb were 5.00–11.36 days in root, 5.07–11.46 days in stem, 6.83–11.31 days in leaf and 6.44–8.43 days in soil. The terminal residues of propamocarb were below the maximum residue limits (MRLs) of EU (0.20 mg kg^?1) and South Korea (0.50 mg kg^?1 in fresh ginseng and 1.0 mg kg^?1 in dried ginseng) over 28 days after last spraying at recommended dosage. The results provide a quantitative basis for establishing the MRL and give a suggestion of safe and reasonable use of propamocarb in ginseng.     

Characterizing ozone pollution in a petrochemical industrial area in Beijing,China: a case study using a chemical reaction model

This study selected a petrochemical industrial complex in Beijing, China, to understand the characteristics of surface ozone (O₃) in this industrial area through the on-site measurement campaign during the July–August of 2010 and 2011, and to reveal the response of local O₃ to its precursors’ emissions through the NCAR-Master Mechanism model (NCAR-MM) simulation. Measurement results showed that the O₃ concentration in this industrial area was significantly higher, with the mean daily average of 124.6 μg/m³ and mean daily maximum of 236.8 μg/m³, which are, respectively, 90.9 and 50.6 % higher than those in Beijing urban area. Moreover, the diurnal O₃ peak generally started up early in 11:00–12:00 and usually remained for 5–6 h, greatly different with the normal diurnal pattern of urban O₃. Then, we used NCAR-MM to simulate the average diurnal variation of photochemical O₃ in sunny days of August 2010 in both industrial and urban areas. A good agreement in O₃ diurnal variation pattern and in O₃ relative level was obtained for both areas. For example of O₃ daily maximum, the calculated value in the industrial area was about 51 % higher than in the urban area, while measured value in the industrial area was approximately 60 % higher than in the urban area. Finally, the sensitivity analysis of photochemical O₃ to its precursors was conducted based on a set of VOCs/NOx emissions cases. Simulation results implied that in the industrial area, the response of O₃ to VOCs was negative and to NOx was positive under the current conditions, with the sensitivity coefficients of ?0.16~?0.43 and +0.04~+0.06, respectively. By contrast, the urban area was within the VOCs-limitation regime, where ozone enhancement in response to increasing VOCs emissions and to decreasing NOx emission. So, we think that the VOCs emissions control for this petrochemical industrial complex will increase the potential risk of local ozone pollution aggravation, but will be helpful to inhibit the ozone formation in Beijing urban area through reducing the VOCs transport from the industrial area to the urban area.     

Characteristics of ambient 1-min PM2.5 variation in Beijing

One-minute PM_2.5 concentration was obtained with LD-5C pocket microcomputer laser dust instrument from Dec. 15th, 2005 to Jan. 16th, 2006 and Mar. 17th to Apr. 28th, 2006 in Beijing. The concentration of SO₂, NO₂, O₃, CO, and PM₁₀ from Jan. 1st, 2001 to Dec. 31st, 2004 were obtained from the conversion of air pollution index. Results showed that all the pollutants showed cyclic characteristics. The longer yearly cycles was shown from SO₂, NO₂, O₃, CO, and PM₁₀, as the sampling time was 4-year long and daily collected. The shorter hourly and daily cycle was shown from 1-min PM_2.5, as the sampling time was about 1-month long and one collected at 1 min. The spectral density analysis confirmed this from the periodogram graphs. The longer yearly cycle (365, 180 days), the seasonal cycle (120, 60–90 days), and monthly cycle (21, 23, 27 days) of SO₂, NO₂, CO, O₃, and PM₁₀ were obviously shown. In addition, the shorter weekly cycle of 5–7 days is obviously shown, too. The shorter hourly cycle (8–12, 4–6, 3, 1–2 h, 20 min) of 1-min PM_2.5 was also indicated from spectral density analysis. Two major factors contribute the 1-min PM_2.5 cycles, i.e., the meteorological factors and source effects. Both the relative humidity and dew point showed consistent variation with PM_2.5, but the wind speed showed inverse variations with PM_2.5. Furthermore, the spectral density analysis of the meteorological factors (4–5, 2–2.5, 1–1.5 days, 12, 6–8, 3 h) may partially explain the cycles of PM_2.5. As for the sources effects, it can be shown from the strong dust storm of April 16–18th, 2006. PM_2.5 constantly increased tens and even hundreds of times high concentration within a few minutes due to the intensity of the dust sources.     

大气超级站网建设及在江苏区域的集成应用实践

当前全球大气环境问题趋于复杂化,区域性灰霾、酸雨和以臭氧、二次有机气溶胶生成为主的光化学污染问题成为大气环境保护领域关注的重点、热点问题。江苏省大气污染由过去单一的煤烟型污染逐步转变为多种污染物、多种作用机制同时存在且相互影响的复合型污染,成为影响广大人民群众身体健康和生态文明发展的重要因素。笔者对欧美和中国关于大气超级站网设计和建设进行了简要评述和比较分析,提出适合江苏省环境监测体系现状的大气复合型超级站网建设、区域数据综合集成及应用发展等方面的建设理论。