Should Habitat Trading Be Based on Mitigation Ratios Derived from Landscape Indices? A Model-Based Analysis of Compensatory Restoration Options for the Red-Cockaded Woodpecker

Many species of conservation concern are spatially structured and require dispersal to be persistent. For such species, altering the distribution of suitable habitats on the landscape can affect population dynamics in ways that are difficult to predict from simple models. We argue that for such species, individual-based and spatially explicit population models (SEPMs) should be used to determine appropriate levels of off-site restoration to compensate for on-site loss of ecologic resources. Such approaches are necessary when interactions between biologic processes occur at different spatial scales (i.e., local [recruitment] and landscape [migration]). The sites of restoration and habitat loss may be linked to each other, but, more importantly, they may be linked to other resources in the landscape by regional biologic processes, primarily migration. The common management approach for determining appropriate levels of off-site restoration is to derive mitigation ratios based on best professional judgment or pre-existing data. Mitigation ratios assume that the ecologic benefits at the site of restoration are independent of the ecologic costs at the site of habitat loss. Using an SEPM for endangered red-cockaded woodpeckers, we show that the spatial configuration of habitat restoration can simultaneously influence both the rate of recruitment within breeding groups and the rate of migration among groups, implying that simple mitigation ratios may be inadequate.     

pH、温度和水土比对酸性土壤溶液中铝离子形态分布的影响

溶液中Al3 、Al-F和有机络合态铝（Al-OM的浓度随pH降低而增加,Al3 在总单核铝中所占比例随pH的降低而增加,而Al-F络合物呈相反的变化趋势.土壤中铝的溶解度与土壤中铝氧化物的结晶形态有关,处于较高纬度地区的土壤,由于铝氧化物的结晶形态较差,在相同pH下,其铝的溶解度较大.土壤溶液中有机络合态铝的浓度随温度升高而增加,在pH不变的情况下,土壤中无机铝的溶解量随温度降低而增加.随水土比增加,土壤溶液中Al3 、Al-F络合物和Al-OM浓度减小,但按每kg土计算的铝溶解量随水土比的增加而增加.     

Phytotoxicities of fluoranthene and phenanthrene deposited on needle surfaces of the evergreen conifer, Japanese red pine (Pinus densiflora Sieb. et Zucc.)

Polycyclic aromatic hydrocarbons (PAHs) have been widely studied with respect to their carcinogenic and mutagenic effects on animals and human cells. Phenanthrene (PHE) and fluoranthene (FLU) effects on the needle photosynthetic traits of 2-year-old Japanese red pine (Pinus densiflora Sieb. et. Zucc.) seedlings were investigated. Three months after fumigation of foliage with solutions containing these PAHs (10 microM each), FLU had negative effects on net photosynthesis at near-saturating irradiance, stomatal conductance, initial chlorophyll fluorescence, and the contents of total chlorophyll, magnesium, and ribulose 1,5-bisphosphate carboxylase (rubisco) of current-year needles. PHE had similar negative effects to FLU but in lesser magnitude. The effects of the PAHs were mitigated by the addition of an OH-radical scavenger (mannitol) into the PAH solutions. PAHs deposited on the surface of pine needles may induce the generation of reactive oxygen species in the photosynthetic apparatus, a manner closely resembling the action of the herbicide paraquat.     

Biological effect monitoring in dab (<Emphasis Type="Italic">Limanda limanda</Emphasis>) using gene transcript of CYP1A1 or EROD—a comparison

BACKGROUND, AIM, AND SCOPE: Gene expression analyses with real-time (RT)-polymerase chain reaction (PCR) gains importance in marine monitoring. This new technique has to be compared to the classical approaches like the well known biomarker ethoxyresorufin-O-deethylase (EROD) to test their suitability for monitoring programmes. The goal of the present study is to compare EROD activity and CYP1A1 mRNA expression in the important monitoring fish species dab (Limanda limanda) and to answer the question of whether these parameters reflect the polycyclic aromatic hydrocarbon (PAH) contamination of the fish. Further on, glyceraldehyd-3-phosphate dehydrogenase (GAPDH) was investigated as a potential housekeeping gene. MATERIALS AND METHODS: Female dab were caught in the summer of 2004 in the North Sea and in the Baltic. EROD activity was determined in liver samples by a kinetic fluorimetric assay according to a standard protocol. The gene expression of CYP1A (cytochrome P450 1A) and GAPDH were determined by means of RT-PCR. Results were compared to gonado somatic index and to the concentration of PAH metabolite 1OHPyr (1-hydroxypyrene) analysed in the bile fluids of the fish, respectively. RESULTS: Dab from all stations showed a considerable individual variation in the levels of both CYP1A mRNA and EROD. Highest mean values for CYP1A mRNA and EROD were detected in the northern part of the sampling area. In contrast, the PAH metabolite 1OHPyr was found at the highest concentration in fish caught near the German coast. CYP1A mRNA and EROD showed only a minor but significant correlation (r = 0.32, p < 0.05, n = 123). 1OHPyr in bile correlated significantly (p < 0.05) with the amount of GAPDH mRNA content in the liver. DISCUSSION: The significant but low correlation of CYP1A mRNA and EROD activity on an individual basis illustrates that these two parameters are apparently not closely linked. However, maximum EROD values correspond with maximum CYP1A mRNA concentrations when station means are regarded. Because EROD and CYP1A mRNA in dab follow different physiological principles, their application will lead to related but not identical monitoring results. This should be taken into account when future marine monitoring programmes are designed. The results also indicate that PAH are not the crucial factor for CYP1A and EROD levels in dab from the off-shore areas in the North Sea. This is remarkable because the PAH metabolism is known to be CYP1A-dependent and the widely used biomarker EROD has been recommended for monitoring PAH-related effects in fish from the North Sea. Due to a correlation between GAPDH and 1OHPyr, GAPDH was not suitable as housekeeping gene for dab. CONCLUSIONS: Neither the results from EROD nor from CYP1A1 mRNA measurements in dab reflected their exposure to PAH as measured by the PAH metabolite 1OHPyr. Thus, the question arises of whether EROD or CYP1A mRNA is a suitable biomarker at all to indicate PAH exposure in dab from the open North Sea. RECOMMENDATIONS AND PERSPECTIVES: For future biological effect monitoring, it is advisable to measure more and predominately independent parameters by RT-PCR and to incorporate more components of the detoxification system.     

Monitoring of environmental exposure to polycyclic aromatic hydrocarbons: a review

Polycyclic aromatic hydrocarbons (PAHs) are a large group of organic compounds with two or more fused aromatic rings. They have a relatively low solubility in water, but are highly lipophilic. Most of the PAHs with low vapour pressure in the air are adsorbed on particles. When dissolved in water or adsorbed on particulate matter, PAHs can undergo photodecomposition when exposed to ultraviolet light from solar radiation. In the atmosphere, PAHs can react with pollutants such as ozone, nitrogen oxides and sulfur dioxide, yielding diones, nitro- and dinitro-PAHs, and sulfonic acids, respectively. PAHs may also be degraded by some microorganisms in the soil. PAHs are widespread environmental contaminants resulting from incomplete combustion of organic materials. The occurrence is largely a result of anthropogenic emissions such as fossil fuel-burning, motor vehicle, waste incinerator, oil refining, coke and asphalt production, and aluminum production, etc. PAHs have received increased attention in recent years in air pollution studies because some of these compounds are highly carcinogenic or mutagenic. Eight PAHs (Car-PAHs) typically considered as possible carcinogens are: benzo(a)anthracene, chrysene, benzo(b)fluoranthene, benzo(k)fluoranthene, benzo(a)pyrene (B(a)P), dibenzo(a,h)anthracene, indeno(1,2,3-cd)pyrene and benzo(g,h,i)perylene. In particular, benzo(a)pyrene has been identified as being highly carcinogenic. The US Environmental Protection Agency (EPA) has promulgated 16 unsubstituted PAHs (EPA-PAH) as priority pollutants. Thus, exposure assessments of PAHs in the developing world are important. The scope of this review will be to give an overview of PAH concentrations in various environmental samples and to discuss the advantages and limitations of applying these parameters in the assessment of environmental risks in ecosystems and human health. As it well known, there is an increasing trend to use the behavior of pollutants (i.e. bioaccumulation) as well as pollution-induced biological and biochemical effects on human organisms to evaluate or predict the impact of chemicals on ecosystems. Emphasis in this review will, therefore, be placed on the use of bioaccumulation and biomarker responses in air, soil, water and food, as monitoring tools for the assessment of the risks and hazards of PAH concentrations for the ecosystem, as well as on its limitations.     

Polycyclic aromatic hydrocarbons, black carbon, and molecular markers in soils of Switzerland

Polycyclic aromatic hydrocarbons (PAH) were analysed in 23 soil samples (0–10 cm layer) from the Swiss soil monitoring network (NABO) together with total organic carbon (TOC) and black carbon (BC) concentration, as well as some PAH source diagnostic ratios and molecular markers. The concentrations of the sum of 16 EPA priority PAHs ranged from 50 to 619 μg/kg dw. Concentrations increased from arable, permanent and pasture grassland, forest, to urban soils and were 21–89% lower than median numbers reported in the literature for similar Swiss and European soils. NABO soils contained BC in concentrations from 0.4 to 1.8 mg/g dw, except for two sites with markedly higher levels. These numbers corresponded to 1–6% of TOC and were comparable to the limited published BC data in soil and sediments obtained with comparable analytical methods. The various PAH ratios and molecular markers pointed to a domination of pyrogenically formed PAHs in Swiss soils. In concert, the gathered data suggest the following major findings: (1) gas phase PAHs (naphthalene to fluorene) were long-range transported, cold-condensated at higher altitudes, and approaching equilibrium with soil organic matter (OM); (2) (partially) particle-bound PAHs (phenanthrene to benzo[ghi]perylene) were mostly deposited regionally in urban areas, and not equilibrated with soil OM; (3) Diesel combustion appeared to be a major emission source of PAH and BC in urban areas; and (4) wood combustion might have contributed significantly to PAH burdens in some soils of remote/alpine (forest) sites.     

潮白河周丛生物群落元素组成与水质变化的生态计量学关系研究

研究了潮白河流域中污染水体对周丛生物群落的碳(C)、氮(N)、磷(P)元素含量以及生态计量组成的影响.结果表明,下游潮白河NH4+-N、NOx--N分别占TN的52%和28%;上游白河则分别占1.6%和38%.潮白河TP含量(0.104 mg.L-1)为白河TP含量(0.005 mg.L-1)的21倍.白河和潮白河周丛生物C、N、P元素的变异系数分别为0.55、0.41、0.62和0.24、0.13、0.18,表明生长于白河周丛生物的元素结构变化更大.无周丛生物的水体NH4+-N和TP的浓度分别为有周丛生物的21倍和11倍.通过对TOC、TN、NOx--N、NH4+-N、TP、pH、氧化还原电位(ORP)和电导率(conductivity)等水质指标进行二元Logistic回归分析得知,水体TP为影响潮白河周丛生物生存的主要因素,其预测正确率为87.3%.周丛生物C、N、P元素间有强相关性,其中N起了"桥梁"作用.生态计量学分析进一步显示周丛生物的N∶P的比值追随水体TN∶TP的变化;并且该比值主要受水体TP浓度影响.周丛生物N∶P可用于水体TN∶TP变化的生态计量学的指示因子.本研究为进一步探究周丛生物群落结构变化,以及对高一级营养级生物群落结构和元素循环的影响奠定了基础.     

Multi-factors influencing the spatial distribution of polycyclic aromatic hydrocarbons in soils surrounding drinking water protection zone

We selected the Guanting Reservoir in Beijing, China as a case where an industrial area locates on the upwind corner to study the influence of human activities and natural processes on the distribution of polycyclic aromatic hydrocarbons (PAHs) in soils. Soil PAH concentrations in the study area follow a log-normal probability distribution function, suggesting that distribution of PAH in soils was affected by human activities. Distribution of PAHs in soils was significantly affected by the point source that high PAH concentrations were observed in near industrial area with an obvious declining trend from the northwest to the southeast which was the prevailing wind direction in this area. Away from the influence of point source, distribution of PAHs in soils was found to significantly correlate with total organic carbon content, while the influences of agricultural land uses and type of soil texture on the total soil PAHs contents and ring compositions were quite limited. The results can provide some evidences and data on the pollutant accumulation in drink water protection area influenced by natural processes and human activities.     

基于SOA和O3生成潜势的杭州市PM2.5和O3协同控制

2019年3月1日～2019年5月31日期间采用Syntech Spectras GC955在线气相色谱仪对杭州市大气环境中挥发性有机物（VOCs）进行了在线连续监测,分析了VOCs体积分数的组成特征、 PM_2.5和O₃协同控制的优控VOCs物种和VOCs特征污染物比值.结果表明,烷烃是VOCs体积分数中最重要的组分,贡献了62.40%. C2～C6的烷烃、苯系物、乙烯和乙炔是VOCs关键物种.烯烃和芳香烃是OFP的主要贡献组分,贡献率分别为41.35%和37.50%.芳香烃是SOA的主要贡献者,贡献率超过90%.低碳的烷烃、低碳烯烃和苯系物是OFP的关键贡献物种,控制好甲苯、间/对-二甲苯和邻-二甲苯这3种苯系物,是O₃和PM_2.5协同控制的关键.采样点大气中VOCs除了受机动车尾气的影响外,溶剂使用等工业排放的影响也较为显著.     

青藏高原淡水湖泊水化学组成特征及其演化

青藏高原淡水湖具有高生态价值和高脆弱性并存的特点.以海拔5 080 m±10 m的打加芒错湖水为研究对象,测试及分析了湖水化学组分,探讨了其主要离子来源、控制因子和湖泊水化学演化趋势.结果表明,湖水阳离子以Ca2+和Na+为主,阴离子以HCO3-为主,为HCO3-Ca型水;TDS为71.2～199.8 mg·L-1,矿化度低;受地表径流的稀释作用和富铝贫钙的地质背景约束湖区东南部水体的EC、Ca2+和HCO3-浓度均较低.湖水的Na+/(Na++Ca2+)为0.08～0.75,Cl-/(Cl-+HCO3-)为0.11～0.35,Ca/Na值为0.58,Mg/Ca值为0.12,HCO3/Na值为1.46,据Gibbs模型和元素化学计量分析表明,其化学组成主要受硅酸盐岩风化控制.湖区流域参与风化的矿物岩石包括斜长石(钙长石、钠长石)、钾长石、云母、石膏、盐岩等,但以斜长石风化为主,湖水的K/Na值平均为0.059,表明流域钾长石风化程度较低.湖水中方解石、白云石、石英、石膏等矿物饱和指数(SI)大于0,石盐的SI则小于0,揭示了青藏高原上淡水湖泊演变成咸水湖的变化趋势.