Department of Environmental Sciences, University of Peshawar, 25120, Peshawar, Pakistan.
Environ Sci Pollut Res Int. 2010 Feb;17(2):288-96. doi: 10.1007/s11356-009-0134-4. Epub 2009 Mar 31.
BACKGROUND, AIM, AND SCOPE: Soil contamination with heavy metals occurs as a result of both anthropogenic and natural activities. Heavy metals could have long-term hazardous impacts on the health of soil ecosystems and adverse influences on soil biological processes. Soil enzymatic activities are recognized as sensors towards any natural and anthropogenic disturbance occurring in the soil ecosystem. Similarly, microbial biomass carbon (MBC) is also considered as one of the important soil biological activities frequently influenced by heavy metal contamination. The polymerase chain reaction-denaturing gradient gel electrophoresis (DGGE) has recently been used to investigate changes in soil microbial community composition in response to environmental stresses. Soil microbial community structure and activities are difficult to elucidate using single monitoring approach; therefore, for a better insight and complete depiction of the soil microbial situation, different approaches need to be used. This study was conducted in a greenhouse for a period of 12 weeks to evaluate the changes in indigenous microbial community structure and activities in the soil amended with different application rates of Cd, Pb, and Cd/Pb mix. In a field environment, soil is contaminated with single or mixed heavy metals; so that, in this research, we used the selected metals in both single and mixed forms at different application rates and investigated their toxic effects on microbial community structure and activities, using soil enzyme assays, plate counting, and advanced molecular DGGE technique. Soil microbial activities, including acid phosphatase (ACP), urease (URE), and MBC, and microbial community structure were studied.
A soil sample (0-20 cm) with an unknown history of heavy metal contamination was collected and amended with Cd, Pb, and Cd/Pb mix using the CdSO(4) and Pb(NO(3))(2) solutions at different application rates. The amended soils were incubated in the greenhouse at 25 +/- 4 degrees C and 60% water-holding capacity for 12 weeks. During the incubation period, samples were collected from each pot at 0, 2, 9, and 12 weeks for enzyme assays, MBC, numeration of microbes, and DNA extraction. Fumigation-extraction method was used to measure the MBC, while plate counting techniques were used to numerate viable heterotrophic bacteria, fungi, and actinomycetes. Soil DNAs were extracted from the samples and used for DGGE analysis.
ACP, URE, and MBC activities of microbial community were significantly lower (p < 0.05) in the metal-amended samples than those in the control. The enzyme inhibition extent was obvious between different incubation periods and varied as the incubation proceeded, and the highest rate was detected in the samples after 2 weeks. However, the lowest values of ACP and URE activities (35.6% and 36.6% of the control, respectively) were found in the Cd(3)/Pb(3)-treated sample after 2 weeks. Similarly, MBC was strongly decreased in both Cd/Pb-amended samples and highest reduction (52.4%) was detected for Cd(3)/Pb(3) treatment. The number of bacteria and actinomycetes were significantly decreased in the heavy metal-amended samples compared to the control, while fungal cells were not significantly different (from 2.3% to 23.87%). In this study, the DGGE profile indicated that the high dose of metal amendment caused a greater change in the number of bands. DGGE banding patterns confirmed that the addition of metals had a significant impact on microbial community structure.
In soil ecosystem, heavy metals exhibit toxicological effects on soil microbes which may lead to the decrease of their numbers and activities. This study demonstrated that toxicological effects of heavy metals on soil microbial community structure and activities depend largely on the type and concentration of metal and incubation time. The inhibition extent varied widely among different incubation periods for these enzymes. Furthermore, the rapid inhibition in microbial activities such as ACP, URE, and MBC were observed in the 2 weeks, which should be related to the fact that the microbes were suddenly exposed to heavy metals. The increased inhibition of soil microbial activities is likely to be related to tolerance and adaptation of the microbial community, concentration of pollutants, and mechanisms of heavy metals. The DGGE profile has shown that the structure of the bacterial community changed in amended heavy metal samples. In this research, the microbial community structure was highly affected, consistent with the lower microbial activities in different levels of heavy metals. Furthermore, a great community change in this study, particularly at a high level of contamination, was probably a result of metal toxicity and also unavailability of nutrients because no nutrients were supplied during the whole incubation period.
The added concentrations of heavy metals have changed the soil microbial community structure and activities. The highest inhibitory effects on soil microbial activities were observed at 2 weeks of incubation. The bacteria were more sensitive than actinomycetes and fungi. The DGGE profile indicated that bacterial community structure was changed in the Cd/Pb-amended samples, particularly at high concentrations.
The investigation of soil microbial community structure and activities together could give more reliable and accurate information about the toxic effects of heavy metals on soil health.
背景、目的和范围:土壤重金属污染是人为和自然活动的结果。重金属可能对土壤生态系统的健康产生长期的有害影响,并对土壤生物过程产生不利影响。土壤酶活性被认为是对土壤生态系统中任何自然和人为干扰的敏感指标。同样,微生物生物量碳(MBC)也被认为是受重金属污染影响的重要土壤生物活性之一。聚合酶链反应-变性梯度凝胶电泳(DGGE)最近被用于研究环境胁迫下土壤微生物群落组成的变化。土壤微生物群落结构和活性很难通过单一监测方法来阐明;因此,为了更好地了解和全面描述土壤微生物状况,需要使用不同的方法。本研究在温室中进行了 12 周,以评估不同镉、铅和镉/铅混合应用率下土壤中土著微生物群落结构和活性的变化。在野外环境中,土壤受到单一或混合重金属的污染;因此,在这项研究中,我们使用了选定的金属以单一和混合形式在不同的应用率下,并使用土壤酶分析、平板计数和先进的分子 DGGE 技术研究了它们对微生物群落结构和活性的毒性影响。研究了土壤微生物活性,包括酸性磷酸酶(ACP)、脲酶(URE)和 MBC,以及微生物群落结构。
采集了一份未知重金属污染历史的土壤样本(0-20cm),并用 CdSO4和 Pb(NO3)2溶液以不同的应用率添加了 Cd、Pb 和 Cd/Pb 混合物。添加了重金属的土壤在 25±4°C 和 60%持水能力的温室中培养 12 周。在培养期间,从每个盆中在 0、2、9 和 12 周时采集样品进行酶分析、MBC、微生物计数和 DNA 提取。使用熏蒸提取法测量 MBC,而平板计数技术用于计数可培养的异养细菌、真菌和放线菌。从样品中提取土壤 DNA,并用于 DGGE 分析。
与对照相比,金属添加样品中的 ACP、URE 和 MBC 微生物群落活性显著降低(p<0.05)。不同培养期间的酶抑制程度明显不同,随着培养的进行而变化,在培养 2 周时检测到最高速率。然而,在 2 周后 Cd(3)/Pb(3)处理的样品中,ACP 和 URE 活性的最低值分别为对照的 35.6%和 36.6%。同样,Cd/Pb 处理的土壤中 MBC 也明显减少,最高减少(52.4%)发生在 Cd(3)/Pb(3)处理中。与对照相比,重金属添加样品中的细菌和放线菌数量显著减少,而真菌细胞数量没有显著差异(从 2.3%到 23.87%)。在这项研究中,DGGE 图谱表明高剂量的金属添加导致带的数量发生了更大的变化。DGGE 带型证实,金属对微生物群落结构有显著影响。
在土壤生态系统中,重金属对土壤微生物表现出毒性作用,可能导致其数量和活性的减少。本研究表明,重金属对土壤微生物群落结构和活性的毒性影响在很大程度上取决于金属的类型和浓度以及培养时间。不同培养期间这些酶的抑制程度差异很大。此外,在 2 周内,ACP、URE 和 MBC 等微生物活性迅速抑制,这可能与微生物突然暴露于重金属有关。土壤微生物活性的抑制增加可能与微生物群落的耐受性和适应性、污染物浓度和重金属的机制有关。DGGE 图谱显示,添加重金属的样品中细菌群落结构发生了变化。在这项研究中,微生物群落结构受到了高度影响,与不同水平重金属下微生物活性的降低一致。此外,在高污染水平下,群落的巨大变化可能是由于金属毒性和缺乏营养物质,因为在整个培养期间没有提供营养物质。
添加的重金属浓度改变了土壤微生物群落结构和活性。在培养 2 周时,对土壤微生物活性的抑制作用最大。细菌比放线菌和真菌更敏感。DGGE 图谱表明,在 Cd/Pb 处理的样品中,细菌群落结构发生了变化,特别是在高浓度下。
土壤微生物群落结构和活性的综合研究可以提供更可靠和准确的关于重金属对土壤健康的毒性影响的信息。