雄黄矿区不同砷污染土壤中微生物群落结构及碳源利用特征

土壤砷污染是我国乃至世界范围内比较严重的环境问题.有关砷污染的生态毒理效应有很多研究,但对砷污染土壤中微生物群落的关注相对较少.本文以我国湖南省石门县雄黄矿地区长期砷污染土壤为例,采用PLFA及BIOLOG微平板技术考察了7个砷(As)污染程度不同的样点以及一个对照样点土壤微生物群落结构及碳源利用特征.结果发现,雄黄矿区存在多种重金属复合污染,除As含量较高以外,镉(Cd)和镍(Ni)的含量也超过了国家土壤环境质量三级标准.雄黄矿区土壤微生物的群落结构受到土壤有机碳(SOC)、有效磷(AP)、p H以及镁(Mg)、Cd、铁(Fe)、铜(Cu)含量的显著影响.各样点土壤微生物群落均以细菌为主,占微生物总量的71.54%~80.66%,真菌次之,放线菌最少.雄黄矿区土壤中的有效砷对微生物造成了较严重的胁迫.严重砷污染降低了微生物对于碳源利用的多样性以及均匀度.各样点微生物对于碳源的利用也表现出明显的差异.31种碳源中微生物利用较多的只有7类,分别属于糖类、胺类、羧酸类与多聚物,并且以糖类为主.     

Effect of low-molecular weight organic acids on phosphorus release and phytoavailabilty of phosphorus in phosphate rocks added to soils

Phosphorus (P) is critically needed to improve soil fertility in many parts of the world. The use of water-soluble P fertilizers, e.g., single super-phosphate and triple super-phosphate in developing countries to improve crop production has been limited primarily by their high cost. The presence of indigenous phosphate deposits in some countries provides an incentive for direct application or local chemical treatment at low cost to improve the solubility of low reactive phosphate rocks (PRs). The use of naturally occurring low-molecular weight organic acids (LMWOAs) that are produced in soil as microbial metabolites or plant exudates from dead or living cells represents a new perspective in PR research. The LMWOAs contain various functional groups that may play a significant role in PR dissolution. Little information is available, however, about the potential of LMWOAs in releasing P from PRs. This study reports P release from 12 PRs, four each of low, medium, and high reactivity, obtained from various deposits (Kodjari, Tahoua, North Carolina, Gafsa, Khouribga, Tilemsi Valley, Central Florida, Sechura, Minjingu, North Florida, Hahotoe, and Parc W) using nine LMWOAs containing mono-, di-, and tri-carboxylic groups and a mineral acid (H₂SO₄). Laboratory studies showed that the organic acids are effective in releasing P from low and medium reactive PRs, but very ineffective in releasing P from high reactive PRs. The average amounts of P released by all the organic acids from the three types of PRs were 65.5 mmol kg⁻¹ PR from the low reactive PRs, 55.1 mmol kg⁻¹ from the medium, and 11.1 mmol kg⁻¹ from the high; those released from across all the PRs were 21.9 by the mono-carboxylic acid group, 54.2 by the di-carboxylic acid group, and 57.0 mmol P kg⁻¹ by the tri-carboxylic acid group. The P released was negatively correlated with the equilibrium pH, but positively correlated with Ca released from the PRs. Laboratory incubation studies on the release of P from PRs added to soils with or without organic acids and incubated at 25 °C for 15, 30, and 45 days showed that the percentage of plant-available P released varied considerably from 0.95 in the Kodjari PR to 40.1% in the North Carolina PR and was related to PR reactivity. A greenhouse study with corn (Zea mays L.) grown for 60 days on soils treated with PRs or with PRs mixed with organic acids showed that corn response to addition of oxalic or citric acid varied with P rates and PR sources, suggesting that organic acids have potential as amendments for increasing plant-available P in PR-treated soils.     

Potassium ferrate pretreatment promotes short chain fatty acids yield and antibiotics reduction in acidogenic fermentation of sewage sludge

During the acidogenic fermentation converting waste activated sludge (WAS) into short-chain fatty acids (SCFA), hydrolysis of complex organic polymers is a limiting step and the transformation of harmful substances (such as antibiotics) during acidogenic fermentation is unknown. In this study, potassium ferrate (K₂FeO₄) oxidation was used as a pretreatment strategy for WAS acidogenic fermentation to increase the hydrolysis of sludge and destruct the harmful antibiotics. Pretreatment with K₂FeO₄ can effectively increase the SCFA production during acidogenic fermentation and change the distribution of SCFA components. With the dosage of 0.2 g/g TS, the maximum SCFA yield was 4823 mg COD/L, which is 28.3 times that of the control group; acetic acid accounts for more than 90% of the total SCFA. The higher dosage (0.5 g/g TS) can further increase the proportion of acetic acid, but inhibit the overall performance of SCFA production. Apart from the promotion of hydrolysis and acidogenesis, K₂FeO₄ pretreatment can also simultaneously oxidizes and degrades part of the antibiotics in the sludge. When the dosage is 0.5 g/g TS, the degradation efficacy of antibiotics is the most significant, and the contents of ofloxacin, azithromycin, and tetracycline in the sludge are reduced by 69%, 42%, and 50%, respectively. In addition, K₂FeO₄ pretreatment can also promote the release of antibiotics from sludge flocs, which is conducive to the simultaneous degradation of antibiotics in the subsequent biological treatment process.     

生物酶对初沉污泥厌氧发酵产短链脂肪酸的调控研究

旨在通过生物酶调节(碱性蛋白酶、中性蛋白酶和α-淀粉酶)提高初沉污泥的厌氧发酵效率,并通过微生物群落结构解析,SCFAs (short-chain fatty acids,SCFAs)组分分析等揭示其调控机理.结果表明,3种生物酶均可增强初沉污泥水解和产酸作用,碱性蛋白酶调控系统对初沉污泥厌氧发酵的促进效果最为明显,发酵第4d SCFAs的产量和产率分别达到1508mg COD/L和0.174g COD/g VSS.对比控制组,SCFAs的产量和产率分别增加了1129mg COD/L和0.13g COD/g VSS.微生物群落结构分析表明,在碱性蛋白酶调控发酵系统中,Lentimicrobium、Proteiniphilum和Bacteroides等发酵相关菌群的相对丰度得到了改善,Methanosaeta、Methanospirillum等产甲烷古菌的活性受到了抑制.同时,生物酶调控对促进发酵过程乙酸占比也有促进作用.     

腐殖质胶结团聚体对苯酚的富集特征

为探讨不同腐殖质组分团聚体对苯酚富集能力的影响,应用国际腐殖酸协会（IHSS）推荐方法提取腐殖质,以Ca2+、Al3+、Fe3+为桥键离子,制备了高岭石、蒙脱石不同腐殖质组分团聚体,采用平衡吸附法研究了不同腐殖质组分团聚体对苯酚的富集特征.结果表明:高岭石不同腐殖质组分团聚体对苯酚的饱和吸附量（Q_m）大小依次为FA（富里酸）团聚体[（254.11±5.35）mg/kg] > HA（胡敏酸）团聚体[（186.14±1.61）mg/kg] > HM（胡敏素）团聚体[（120.61±1.67）mg/kg];蒙脱石不同腐殖质组分团聚体对苯酚的饱和吸附量大小依次为FA团聚体[（418.72±19.14）mg/kg）] > HA团聚体[（290.00±13.06）mg/kg）] > HM团聚体[（160.46±4.92）mg/kg）];高岭石不同腐殖质组分团聚体对苯酚的富集系数（ER）大小依次为FA团聚体（2.03±0.07）> HA团聚体（1.91±0.04）> HM团聚体（1.85±0.04）;蒙脱石不同腐殖质组分团聚体对苯酚的富集系数大小依次为FA团聚体（2.50±0.10）> HA团聚体（2.45±0.11）> HM团聚体（1.36±0.04）.研究显示,FA团聚体对苯酚的饱和吸附量和富集系数较大,对苯酚的吸附（富集）作用较强,HM团聚体对苯酚的饱和吸附量和富集系数较小,对苯酚的吸附（富集）作用较弱.不同腐殖质组分团聚体对苯酚的富集能力大小表现为FA团聚体> HA团聚体> HM团聚体.因此,FA团聚体可作为控制受苯酚污染场地土壤的首选修复剂.      

Tissue distribution of perfluoroalkyl acids and health status in wild Mozambique tilapia (Oreochromis mossambicus) from Loskop Dam, Mpumalanga, South Africa

This study examined concentrations of 15 perfluoroalkyl acids (PFAAs) in tissues from male Mozambique tilapia (Oreochromis mossambicus) collected at Loskop Dam, Mpumalanga, South Africa in 2014 and 2016. Nine of the 15 PFAAs were detected frequently and were included in statistical analysis and included two of the most commonly known PFAAs, perfluorooctanesulfonic acid (PFOS) (median, 41.6 ng/g) and perfluorooctanoic acid (PFOA) (median, 0.0825 ng/g). Of the tissues measured, plasma (2016 and 2014 median, 22.2 ng/g) contained the highest PFAA burden followed by (in descending order): liver (median, 11.6 ng/g), kidney (median, 9.04 ng/g), spleen (median, 5.92 ng/g), adipose (median, 2.54 ng/g), and muscle (median, 1.11 ng/g). Loskop Dam tilapia have been affected by an inflammatory disease of the adipose tissue known as pansteatitis, so this study also aimed to investigate relationships between PFAA tissue concentrations and incidence of pansteatitis or fish health status. Results revealed that healthy tilapia exhibited an overall higher (p-value < 0.05) PFAA burden than pansteatitis-affected tilapia across all tissues. Further analysis showed that organs previously noted in the literature to contain the highest PFAA concentrations, such as kidney, liver, and plasma, were the organs driving the difference in PFAA burden between the two tilapia groups. Care must be taken in the interpretations we draw from not only the results of our study, but also other PFAA measurements made on populations (human and wildlife alike) under differing health status.     

黄山PM10中二元羧酸类化合物的季节变化特征及其来源

为研究黄山大气PM_(10)中二元羧酸类化合物的季节变化特征,分别于2015年夏季、冬季在黄山山顶采集PM_(10)样品,并分析二元羧酸、酮羧酸和α-二羰基化合物.结果表明,无论在夏季还是冬季,草酸(HOOC—COOH,C_2)均是浓度最高的二元羧酸,其次是丙二酸(HOOC—CH_2—COOH,C_3)、丁二酸[HOOC—(CH_2)_2—COOH,C_4],这与其它高海拔地区的分子组成是相似的.大部分二元羧酸的浓度呈冬低夏高的季节变化特征,但是冬季己二酸(C_6)和邻苯二甲酸(Ph)的浓度约高于夏季的2倍,表明冬季黄山大气受周边地区所排放的人为污染物的影响更大.作为二元羧酸的重要前体物,乙二醛(Gly)与甲基乙二醛(mGly)的浓度呈冬高夏低的季节变化特征,表明夏季黄山气溶胶的氧化性比冬季强.主成分分析(PCA)结果表明,黄山冬季SOA主要来自人为源的长距离传输,而夏季SOA主要是当地生物源经二次氧化形成.气溶胶无机模型(AIM)的计算结果表明,黄山夏季的C_2主要是经酸催化反应二次形成的.     

零价铁对污泥高温厌氧消化过程中四环素抗性基因及第一类整合子的消减影响

为研究污泥高温厌氧消化过程中零价铁(Fe0)对抗生素抗性基因的消减影响,采用荧光定量PCR方法定量检测了7种四环素抗性基因(TC-ARGs,包括tetA、tetC、tetG、tetM、tetO、tetW和tetX)及第一类整合子int I1基因在厌氧消化过程中的丰度变化,同时检测分析了挥发性脂肪酸(VFAs)的质量浓度变化,并探讨了目标基因与VFAs之间的相关关系.结果表明,适量Fe0(如0.10 g·g~(-1),以Fe0/VSS计)不仅可以强化污泥厌氧消化进程,显著提高总VFAs和乙酸的产生量,而且能够增强TCARGs和int I1基因的消减效果.尽管如此,过量Fe0(如1.17 g·g~(-1),以Fe0/VSS计)对污泥高温厌氧消化过程中TC-ARGs和int I1基因消减的增强效果并不显著,推测可能是由于基因水平转移的发生所导致的.通过相关性分析可知,TC-ARGs(除tetO基因外)和int I1基因与乙酸之间存在显著负相关性,表明乙酸可能对TC-ARGs和int I1基因的消减具有促进作用.     

四海龙湾表层沉积物中有机质的组成特征及其源解析

为研究玛珥湖四海龙湾表层沉积物中有机质的组成特征及来源,采集四海龙湾表层沉积物样品,并对其中的有机质进行了分析. 结果表明,四海龙湾表层沉积物中w(TOC)(TOC为总有机碳)为6.7%、w(TN)为0.6%、δ13C_org(TOC同位素丰度)为-28.0‰、δ15N_total(TN同位素丰度)为2.2‰. 可溶性有机质主要包括脂肪烃、脂肪醇、脂肪酸和GDGTs(甘油二烷基甘油四醚脂)等,其中脂肪酸是可溶性有机质的主要组分,约占可溶性有机质总量的68.8%,主要来源于内源性的藻类和厌氧菌; 脂肪烃主要来源于陆源的C3木本植物;结合态脂肪醇具有明显的内源来源特征,而游离态脂肪醇却呈现陆源来源特征. 四海龙湾沉积物中含有丰富的GDGTs,主要来源于陆源土壤,包括支链类GDGTs和类异戊二烯类GDGTs,其中类异戊二烯类GDGTs以GDGTⅣ和GDGTⅤ为主,但其在四海龙湾沉积物中的含量相对较小. 研究显示,四海龙湾流域陆源是沉积物中可溶性有机质的主要来源,陆源有机质的大量流入改变了四海龙湾的营养水平;不同种类可溶性有机质表现出不同的来源特征,这主要是由于微生物对不同种类有机质降解速率的不同所致,并且导致降解所产生的二次有机质数量也不同.      

生物降解与吸附作用协同去除卤乙酸生成势

评价了生物强化活性炭(BAC)的生物降解与吸附作用协同对消毒副产物前体物质(DBPFP)的控制效果.控制 BAC 的空床接触时间(EBCT)为 20min 时,BAC 对卤乙酸生成势(HAAFP)的去除率达到 59%,而相同条件下,普通颗粒炭(GAC)对其去除率只有 27%.BAC 工艺中微生物数量和微生物活性均明显高于 GAC 工艺.通过微生物降解作用和活性炭吸附作用的协同,BAC 对 HAAFP 的去除率与 EBCT 具有明显的线性相关性(R²=0.9069).BAC 出水中指标 UV254与 HAAFP 也表现出一定的线性相关性(R²=0.7702).