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981.
三十年来的中国泥石流研究 总被引:41,自引:1,他引:41
本文通过对我国泥石流研究成果的总结,结合作者们工作的心得体会,就我国30年来的泥石流研究工作进行回顾与展望;并针对国情和灾情,提出了相应的意见和建议。 相似文献
982.
Cho ST Tsai SH Ravindran A Selvam A Yang SS 《Environmental geochemistry and health》2008,30(3):255-272
To investigate the seasonal variations of microbial ecology in grassland of Tatachia forest, soil properties, microbial populations,
microbial biomass, and 16S rDNA clone library analysis were determined. The soil had temperatures 6.6–18.4°C, pH 3.6–5.1,
total organic carbon 1.11–10.68%, total nitrogen 0.18–0.78%, and C/N ratios 3.46–20.55. Each gram of dry soil contained bacteria,
actinomycetes, fungi, cellulolytic, phosphate-solubilizing microbes, and nitrogen-fixing microbes 4.54 × 104 to 3.79 × 107, 3.43 × 102 to 2.17 × 105, 5.74 × 103 to 3.76 × 106, 1.97 × 103 to 1.34 × 106, 8.49 × 102 to 5.59 × 105, and 3.86 × 102 to 3.75 × 105 CFU, respectively. Each gram of soil contained 117–2,482 μg of microbial biomass carbon, 23–216 μg of microbial biomass nitrogen
and 9–29 μg of DNA. The microbial populations, microbial biomass, and DNA decreased stepwise with the depth of soil, and they
had low values in winter seasons. The microbial populations, microbial biomass carbon, microbial biomass nitrogen, and DNA
at the BW2 horizon were 8.42–17.84, 19.26–64.40, 16.84–61.11, and 31.03–46.26% of those at the O horizon, respectively. When
analyzing 16S rDNA library, members of Proteobacteria, Acidobacteria, Actinobacteria, Bacteroidetes, Chloroflexi, Firmicutes,
candidate division TM1, candidate division TM7, Gammatimonadetes, and Verrucomicrobia were identified. Members of Proteobacteria
(44.4%) and Acidobacteria (33.3%) dominated the clone libraries. Within the phylum Proteobacteria, α-, β-, and γ-Proteobacteria
were most numerous, followed by δ-Proteobacteria. 相似文献
983.
984.
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986.
冬季大气中苯系物污染特征及人体暴露水平分析 总被引:5,自引:5,他引:0
2007年冬季对乌鲁木齐市空气中苯系物(BTX)进行了网格布点监测,并用气相色谱仪进行样品分析. 结果表明:冬季大气中苯(B)、甲苯(T)和二甲苯(X)的质量浓度分别为5.62~20.57,3.40~122.82和2.20~129.15 μg/m3. 与欧洲标准相比,该地区ρ(苯)较高,且部分地区高于欧洲控制标准;而ρ(甲苯)和ρ(二甲苯)较低,达到欧洲目标限值水平. 苯系物质量浓度和空间分布特点较显著,ρ(甲苯)与ρ(二甲苯)的空间分布较为一致,但与ρ(苯)的分布特点不同. 最后通过对苯系物的人口加权大气污染暴露水平进行分析可知,乌鲁木齐市ρ(苯),ρ(甲苯)和ρ(二甲苯)的污染暴露水平在空间分布上较为均匀,但人口密度空间分布不均匀,故与ρ(苯)分布没有显著的相关性. 城区的ρ(苯),ρ(甲苯)和ρ(二甲苯)的人口加权平均值均略低于全市人口加权平均值,说明虽然城区人口密度较高,但其ρ(苯),ρ(甲苯)和ρ(二甲苯)的人口加权污染暴露水平相对较低. 相似文献
987.
In the present work we investigate whether the distribution of energy flows in ecosystems responds to criteria of trophic organization. We analyzed weighted and unweighted food webs estimating, for each node, trophic position (TP), Shannon's index of inflow diversity (H) and individual contribution to the whole average mutual information (AMI). Finally, we performed the same analysis on simulated webs that were constructed using the following criteria: (a) preserving topology and varying link strength; (b) modifying position of links and their intensities. 相似文献
988.
Modeling compensated root water and nutrient uptake 总被引:1,自引:0,他引:1
Plant root water and nutrient uptake is one of the most important processes in subsurface unsaturated flow and transport modeling, as root uptake controls actual plant evapotranspiration, water recharge and nutrient leaching to the groundwater, and exerts a major influence on predictions of global climate models. In general, unsaturated models describe root uptake relatively simple. For example, root water uptake is mostly uncompensated and nutrient uptake is simulated assuming that all uptake is passive, through the water uptake pathway only. We present a new compensated root water and nutrient uptake model, implemented in HYDRUS. The so-called root adaptability factor represents a threshold value above which reduced root water or nutrient uptake in water- or nutrient-stressed parts of the root zone is fully compensated for by increased uptake in other soil regions that are less stressed. Using a critical value of the water stress index, water uptake compensation is proportional to the water stress response function. Total root nutrient uptake is determined from the total of active and passive nutrient uptake. The partitioning between passive and active uptake is controlled by the a priori defined concentration value cmax. Passive nutrient uptake is simulated by multiplying root water uptake with the dissolved nutrient concentration, for soil solution concentration values below cmax. Passive nutrient uptake is thus zero when cmax is equal to zero. As the active nutrient uptake is obtained from the difference between plant nutrient demand and passive nutrient uptake (using Michaelis–Menten kinetics), the presented model thus implies that reduced passive nutrient uptake is compensated for by active nutrient uptake. In addition, the proposed root uptake model includes compensation for active nutrient uptake, in a similar way as used for root water uptake. The proposed root water and nutrient uptake model is demonstrated by several hypothetical examples, for plants supplied by water due to capillary rise from groundwater and surface drip irrigation. 相似文献
989.
990.
EcoTroph (ET) is a model articulated around the idea that the functioning of aquatic ecosystems may be viewed as a biomass flow moving from lower to higher trophic levels, due to predation and ontogenetic processes. Thus, we show that the ecosystem biomass present at a given trophic level may be estimated from two simple equations, one describing biomass flow, the other their kinetics (which quantifies the velocity of biomass transfers towards top predators). The flow kinetic of prey partly depends on the abundance of their predators, and a top-down equation expressing this is included in the model. Based on these relationships, we simulated the impact on a virtual ecosystem of various exploitation patterns. Specifically, we show that the EcoTroph approach is able to mimic the effects of increased fishing effort on ecosystem biomass expected from theory. Particularly, the model exhibits complex patterns observed in field data, notably cascading effects and ‘fishing down the food web’. EcoTroph also provides diagnostic tools for examining the relationships between catch and fishing effort at the ecosystem scale and the effects of strong top-down controls and fast-flow kinetics on ecosystems resilience. Finally, a dynamic version of the model is derived from the steady-state version, thus allowing simulations of time series of ecosystem biomass and catches. Using this dynamic model, we explore the propagation of environmental variability in the food web, and illustrated how exploitation can induce a decrease of ecosystem stability. The potential for applying EcoTroph to specific ecosystems, based on field data, and similarities between EcoTroph and Ecopath with Ecosim (EwE) are finally discussed. 相似文献