Effects of starvation,season, and diet on the free amino acid and protein content of<Emphasis Type="Italic"> Calanus finmarchicus</Emphasis> females

Effects of food availability and season on the free amino acid (FAA) and total protein content of the copepod Calanus finmarchicus females were investigated in two mesocosm experiments on the Norwegian west coast in spring and autumn. Starved C. finmarchicus females showed no change in total FAA content, but the FAA pool composition changed drastically. During the first 10 days of starvation the protein content showed a moderate decline (<2 µg ind ^-1); however, during the following 21 days the total content was drastically reduced, from 63 to 9 µg ind ^-1. This supports the notion of a sequential catabolism of endogenous nutrients during starvation. In females at high food concentrations, the body protein content increased during spring, but decreased during autumn. The FAA pool composition of females differed between spring and autumn in 14 of the 18 FAA investigated. Reduced body protein content and increased proportion of essential free amino acid were observed during starvation. Similar changes were observed in females sampled at the end of the mesocosm experiments in the autumn. The results suggest that mature C. finmarchicus females are in a negative protein balance during autumn, despite high food concentrations, contributing to a lower fitness than in females maturing during the spring.     

The influence of physicochemical parameters on bioaccessibility-adjusted hazard quotients for copper,lead and zinc in different grain size fractions of urban street dusts and soils

When the hazard quotient for ingestion (HQI) of a trace element in soil and dust particles is adjusted for the element’s bioaccessibility, the HQI is typically reduced as compared to its calculation using pseudo-total element concentration. However, those studies have mostly used bulk particles (<2 mm or <250 µm), and the reduction in HQI when expressed as bioaccessible metal may not be similar among particle size fractions, the possibility probed by the present study of street dusts and soils collected in Tehran. The highest Cu, Pb and Zn near-total concentrations occurred in the finest particles of dusts and soils. Bioaccessible concentrations of Cu, Pb and Zn in the particles (mg kg^?1) were obtained using simple bioaccessibility extraction test (SBET). The bioaccessibility (%) did not vary much among near-total concentrations. In the bulk (<250 µm) sample, the bioaccessible concentration of Cu and Pb increased as the pH of sample increased, while Zn bioaccessibility (%) in the bulk particles was influenced by organic matter and cation exchange capacity. X-ray diffraction identified sulfide and sulfate minerals in all of the size-fractionated particles, which are insoluble to slightly soluble in acidic conditions and included most of the Cu and Pb in the samples. The only Zn-bearing mineral identified was hemimorphite, which would be highly soluble in the SBET conditions. The calculated HQI suggested potential non-carcinogenic health risk to children and adults from ingestions of soils and dusts regardless of particle size consideration, in the order of Zn > Pb ≥ Cu. The HQI calculated from near-total metal was not much different for particle size classes relative to bulk particles; however, the bioaccessibility percent-adjusted HQI for Pb was higher for the smaller particles than the bulk. This work is novel in its approach to compare HQI for a bulk sample of particles with its composite particle size fractions.     

Size-dependent characterisation of historical gold mine wastes to examine human pathways of exposure to arsenic and other potentially toxic elements

Abandoned historical gold mining wastes often exist as geographically extensive, unremediated, and poorly contained deposits that contain elevated levels of As and other potentially toxic elements (PTEs). One of the key variables governing human exposure to PTEs in mine waste is particle size. By applying a size-resolved approach to mine waste characterisation, this study reports on the proportions of mine waste relevant to human exposure and mobility, as well as their corresponding PTE concentrations, in four distinct historical mine wastes from the gold province in Central Victoria, Australia. To the best of our knowledge, such a detailed investigation and comparison of historical mining wastes has not been conducted in this mining-affected region. Mass distribution analysis revealed notable proportions of waste material in the readily ingestible size fraction (≤250 µm; 36.1–75.6 %) and the dust size fraction (≤100 µm; 5.9–45.6 %), suggesting a high potential for human exposure and dust mobilisation. Common to all mine waste types were statistically significant inverse trends between particle size and levels of As and Zn. Enrichment of As in the finest investigated size fraction (≤53 µm) is of particular concern as these particles are highly susceptible to long-distance atmospheric transport. Human populations that reside in the prevailing wind direction from a mine waste deposit may be at risk of As exposure via inhalation and/or ingestion pathways. Enrichment of PTEs in the finer size fractions indicates that human health risk assessments based on bulk contaminant concentrations may underestimate potential exposure intensities.     

Carbon partitioning among the first trophic levels in the North Western Adriatic Basin

In the frame of PRISMA II Project samples for plankton analyses were carried out during four cruises (June, 1996; February and June, 1997; February, 1998) in order to assess the relative importance in term of biomasses of the three main size fractions (pico- <2 r µm, nano- 2-20 r µm and micro-plankton >20 r µm). Spatial and temporal distribution of the three plankton fractions were described as abundance and contribution to the total carbon content in an area between Po River mouth and Rimini. The relative contribution of picoplankton resulted higher in the offshore zone, while that of nanoplankton in the inshore waters. In February 1998 microphytoplankton, mainly constituted by diatoms, was very abundant in the inshore waters. Micro-zooplankton was always very scarce. Cluster analyses performed on these data grouped the stations on the basis of their community structure, and agreed with the hydrological features. Small size classes contributed more significantly to the total plankton carbon content in most of the situations. Microplankton fraction contribution was relevant only during spring diatom bloom of February 1998 and with a less extent in the confined coastal summer blooms.     

Human lung injury following exposure to humic substances and humic-like substances

Among the myriad particles the human respiratory tract is exposed to, a significant number are distinctive in that they include humic substances (HS) and humic-like substances (HULIS) as organic components. HS are heterogeneous, amorphous, organic materials which are ubiquitous occurring in all terrestrial and aqueous environments. HULIS are a complex class of organic, macromolecular compounds initially extracted from atmospheric aerosol particles which share some features with HS including an aromatic, polyacidic nature. As a result of having a variety of oxygen-containing functional groups, both HS and HULIS complex metal cations, especially iron. Following particle uptake by cells resident in the lung, host iron will be sequestered by HS- and HULIS-containing particles initiating pathways of inflammation and subsequent fibrosis. It is proposed that (1) human exposures to HS and HULIS of respirable size (<10 µm diameter) are associated with inflammatory and fibrotic lung disease and (2) following retention of particles which include HS and HULIS, the mechanism of cell and tissue injury involves complexation of host iron. Human inflammatory and fibrotic lung injuries following HS and HULIS exposures may include coal workers’ pneumoconiosis, sarcoidosis, and idiopathic pulmonary fibrosis as well as diseases associated with cigarette smoking and exposures to emission and ambient air pollution particles.     

Distribution,geochemistry, and mineralogy of aerosols in the Angouran Mine area,northwest Iran

The Angouran Mine, located in northwest Iran, is the largest Zn–Pb producer in the Middle East. This study was designed to investigate the distribution, geochemistry, and mineralogy of the aerosols in the mining area and to assess their likely health impacts on the local residents. For this purpose, 36 aerosol samples were collected from 2014 to 2015 at nine sites located in mine district and upwind and downwind directions. The concentration of potentially toxic elements in the aerosols was determined using AAS instrument. Size, morphology, and mineralogy of the particles were studied using SEM and EDX spectra. The results indicate that the amount of total suspended particles in upwind, mine district, and downwind sites is 95.5, 463.4 and 287.5 µg/m³, respectively. The concentrations of PM_2.5 in the three locations are 8.9, 134.7, and 51.8 µg/m³, whereas the PM₁₀ contents are 2.9, 74.4, and 15.5 µg/m³, respectively. These observations point to the impact of mining activities on the concentration of aerosols in the local atmosphere. The values of air quality index also show the probable effects of the mining activities on the health of the local populations, especially for allergic peoples. The average concentration of Zn in the samples collected from the mining district (290 µg/kg) is much higher than its value in the upwind sites (27 µg/kg). The highest concentration of As (70 µg/kg), Cd (10 µg/kg), and Pb (3 µg/kg) is in downwind sites, which shows the negative impact of mining activities on the local air quality. Temporally, the highest concentration of the studied elements is recorded in spring season, especially for PM_2.5 collected in downwind stations. Based on the results of SEM and EDX spectra, three groups of minerals, i.e., carbonates, silicates, and sulfides, are present in the aerosol particles, confirming the local source for the aerosols. SEM analyses showed that the aerosol particles with dissimilar chemical composition have different morphologies such as irregular, rounded, elongated, and angular. On the basis of the results, the mining activities in the Angouran Zn–Pb Mine may have various short- and long-term consequences on the public health, especially due to high amount of the finer particles (PM_2.5) and the higher concentration of the potentially toxic elements in PM_2.5 which can penetrate into the lungs.

     

Lead-210 and Beryllium-7 in the Aerosol Particles Around Taiwan Off-Shore Areas

Abstract

Distributions of ²¹⁰Pb and ⁷Be in the aerosol particles of different size fractions were measured around Taiwan offshore areas from October, 1994 to October, 1995. the size distribution and abundance of the aerosol particles showed both spatial and temporal variations. the particle concentrations off northwestern Taiwan were more than twice as those off northeastern Taiwan both in November and March, and the values were much higher in November than in March for both areas. the measured particle concentrations, except for one sample with an unusually high value, ranged from 10 to 83 μOgm ^?3 in the study areas. the ²¹⁰Pb concentrations in the aerosol particles filtered from the air mass varied between 20 × 10^?3 and 72 × 10^?3 dpm m^?3 (1dpm = 0.45 pCi). the ²¹⁰Pb concentrations in the area off southwestern Taiwan appeared somewhat higher than in other areas and were probably contributed by the land air from Taiwan which contains higher ²¹⁰Pb in winter. the ²¹⁰Pb concentrations off northern Taiwan were low in November when the aerosol concentrations were high, but they were high in March when the aerosol concentrations were low.

Based on the ⁷Be monitoring records of 20 years on the aerosol particles of the island by the Taiwan Radiation Monitoring Center, the mean settling rate averaged 0.91, 0.79 and 0.68 cm s^?1, respectively, in northern, central and southern Taiwan. with these values and the ²¹⁰Pb concentrations in the aerosols, the ²¹⁰Pb flux was determined to be between 0.58 and 2.30 dpm cm^?2y^?1, with an average of 1.19 dpm cm^?2y^?1. Excluding the highest value due to its extremely high ²¹⁰Pb and aerosol concentrations, the average is reduced to 1.05 dpm cm^?2y^?1. the activity median diameters (AMD) for ²¹⁰Pb in the study areas were between 0.69 and < 0.49 μM with a mean of 0.5 öm based on ²¹⁰Pb distributions in different particle size fractions. Thus, ²¹⁰Pb was preferentially adsorbed on to the submicron particles. ⁷Be in the study areas showed a good correlation with ²¹⁰Pb in total activity although the two nucides had different sources.     

Occurrence and particle-size distributions of polycyclic aromatic hydrocarbons in the ambient air of coking plant

The purpose of this study was to characterize the occurrence and size distributions of ten species of polycyclic aromatic hydrocarbons (PAHs) in the ambient air of coking plants. Particulate-matter samples of four size fractions, including ≤2.1, 2.1–4.2, 4.2–10.2, and ≥10.2 μm, were collected using a Staplex234 cascade impactor during August 2009 at two coking plants in Shanxi, China. The PAHs were analyzed by a gas chromatograph equipped with a mass-selective detector. The concentrations of total particulate-matter PAHs were 1,412.7 and 2,241.1 ng/m³ for plants I and II, and the distributions showed a peak within the 0.1–2.1 μm size range for plant I and the 0.1–4.2 μm for plant II. The size distributions of individual PAHs (except fluoranthene) exhibited a considerable peak within the 0.1–2.1 μm size range in coking plant I, which can be explained by the gas–particle partition mechanism. The ambient air of the coking plant was heavily polluted by PAHs associated with fine particles (≤2.1 μm), and benzo[b]fluoranthene made the largest contribution to total PAHs. The exposure levels of coking-plant workers to PAHs associated with fine particles were higher than to PAHs associated with coarse particles. Benzo[b]fluoranthene, benzo[a]pyrene, and dibenzo[a,h]anthracene should be the primary pollutants monitored in the coking plant. This research constitutes a significant contribution to assessing the exposure risk of coking-plant workers and providing basic data for PAH standards for ambient air in coking plants.     

In vitro assessment of arsenic mobility in historical mine waste dust using simulated lung fluid

Exposure studies have linked arsenic (As) ingestion with disease in mining-affected populations; however, inhalation of mine waste dust as a pathway for pulmonary toxicity and systemic absorption has received limited attention. A biologically relevant extractant was used to assess the 24-h lung bioaccessibility of As in dust isolated from four distinct types of historical gold mine wastes common to regional Victoria, Australia. Mine waste particles less than 20 µm in size (PM₂₀) were incubated in a simulated lung fluid containing a major surface-active component found in mammalian lungs, dipalmitoylphosphatidylcholine. The supernatants were extracted, and their As contents measured after 1, 2, 4, 8 and 24 h. The resultant As solubility profiles show rapid dissolution followed by a more modest increasing trend, with between 75 and 82% of the total 24-h bioaccessible As released within the first 8 h. These profiles are consistent with the solubility profile of scorodite, a secondary As-bearing phase detected by X-ray diffraction in one of the investigated waste materials. Compared with similar studies, the cumulative As concentrations released at the 24-h time point were extremely low (range 297 ± 6–3983 ± 396 µg L^?1), representing between 0.020 ± 0.002 and 0.036 ± 0.003% of the total As in the PM₂₀.     

北京城市道路积尘多环芳烃的粒度分布特征及其影响因素

对北京城市不同道路类型的道路积尘进行了为期16个月的采样,分别分析了道路尘的粒径、多环芳烃及TOC.道路积尘的粒径呈三峰态分布,<75 μm部分的颗粒所占体积最大,>214 μm部分颗粒所占体积最小.>214 μm这部分颗粒中的多环芳烃质量分数最低,<75μm和75～214μm这两部分颗粒中多环芳烃的质量分数没有显著差异,但由于<75μm部分颗粒所占的体积和质量比例最大,这部分颗粒的多环芳烃累积量所占比例最高.不同道路的积尘粒径存在差异,海淀路和成府路机动车道的积尘颗粒相比自行车道和人行道的颗粒更粗.由于粒径分布的差异和多环芳烃质量分数的差异,不同类型道路的多环芳烃累积量的粒径分布呈现差异.多环芳烃质量分数和累积量的粒度分布也呈现季节差异,冬春季<75 μm颗粒中的多环芳烃质量分数最高,多环芳烃的累积量所占比例也较夏秋季高.在三个粒级中,TOC与多环芳烃质量分数均呈现显著的正相关.高比例的细颗粒及细颗粒中的多环芳烃使得道路积尘再悬浮进入大气以及随湿沉降进入地表径流的环境风险加大.     

焦作市大气颗粒物中水溶性砷的分布特征

利用原子荧光法对焦作市春、夏、秋、冬四季不同粒径大气颗粒物中水溶性重金属砷的分布特征及时空变化进行分析研究。研究表明：焦作市水溶性砷主要富集在PM2.1中,且颗粒物粒径越小,其富集砷的能力就越强,各级颗粒物中4级、5级、6级（0.41～2.1μm）范围内砷的含量最高,其总含量约为5.71～19.96 ng/m3,三者在不同月份所占比例高达73%～86%;由于形成机制与影响条件不同,不同粒径大气颗粒物中砷表现出明显的季节变化特征,总体趋势为冬季〉秋季〉夏季〉春季,主要原因为冬、夏季燃煤量增加,春季大气污染源减少,地表植被覆盖密集,空气环境质量较好;燃煤是焦作大气中砷的主要来源之一,且其对大气细颗粒物（粒径≤2.1μm）中砷的贡献最明显。     

Chemical fractionation and mobility of traffic-related elements in road environments

Due to considerable progress in exhaust control emission technology and extensive regulatory work regarding this issue, non-exhaust sources of air pollution have become a growing concern. This research involved studying three types of road environment samples such as road dust, sludge from storm drains and roadside soil collected from heavily congested and polluted cities in Poland (Krakow, Warszawa, Opole and Wroclaw). Particles below 20 µm were examined since it was previously estimated that this fine fraction of road dust is polluted mostly by metals derived from non-exhaust sources of pollution such as brake linings wear. Chemical analysis of all samples was combined with a fractionation study using BCR protocol. It was concluded that the finest fractions of road environment samples were significantly contaminated with all of the investigated metals, in particular with Zn, Cu, both well-known key tracers of brake and tire wear. In Warszawa, the pollution index for Zn was on average 15–18 times the background value, in Krakow 12 times, in Wroclaw 8–12 times and in Opole 6–9 times the background value. The pollution index for Cu was on average 6–14 times the background in Warszawa, 7–8 times in Krakow, 4–6 times in Wroclaw and in Opole 5 times the background value. Fractionation study revealed that mobility of examined metals decreases in that order: Zn (43–62%) > Cd (25–42%) > Ni (6–16%) > Cu (3–14%) > Pb (1–8%). It should, however, be noted that metals even when not mobile in the environment can become a serious health concern when ingested or inhaled.     

Urban sediment contamination in a former Hg mining district,Idrija, Slovenia

Road sediments from gully pots of the drainage system and stream sediments from local streams were investigated for the first time in the urban area of Idrija town, the central part of the second largest and strongly contaminated Hg mining district in the world. Hg concentrations in road sediments were lower than in stream sediments. They ranged from 16 to 110 mg/kg (Md = 29 mg/kg) for <0.125 mm particles and from 7 to 125 mg/kg (Md = 35 mg/kg) for <0.04 mm particles, while Hg concentrations in stream sediments ranged from 10 to 610 mg/kg (Md = 95 mg/kg) for <0.125 particles and from 10 to 440 mg/kg (Md = 105 mg/kg) for <0.04 mm particles. High Hg loadings in stream sediments were successfully linked with identified mercury sources (rocks containing mercury ore, areas of former ore roasting sites, ore residue dumps), because they are located in the drainage areas of streams, from which the sediments were collected. Links between Hg loadings in road sediments and identified mercury sources were not recognized. Solid phases of Hg were determined by thermo-desorption technique and are similar for both types of sediments. Results show the occurrence of three different forms: elemental mercury, mercury bound to matrix components and cinnabar. Approximately 50 % of Hg in samples consist of non-cinnabar fractions. This is important, since they are potentially bioavailable. An interesting new discovery according to previous research of environmental media from Idrija area by solid-phase Hg thermo-desorption technique is that elemental mercury was determined in almost all investigated sediments in minor amounts (Md = 3 %).     

Deposition and resorption of organic aerosol constituents in the respiratory tract as calculated from particle size distribution data

Data on the particle size distributions of organic aerosol constituents were used as input for a study, designed to calculate the fractions of the particulate concentrations of these compounds, deposited into the respiratory tract. The known relation between the deposition probability and the particle size as described by the ICRP‐model was used. The organic constituents were from the classes of the aliphatic hydrocarbons, carboxylic acids, polycyclic and aza‐heterocyclic aromatic hydrocarbons. Aerosol samples were obtained by Hi‐Vol cascade impactor sampling at suburban, rural and sea shore background stations as well as in an industrial emission site (coke oven).

Our approach uses the measured concentrations, being average values within each impactor particle size interval, as well as the integrated average deposition probabilities. This procedure was validated experimentally for eight model distributions from the literature, for which an infinitesimal calculation of the deposited fractions was possible.

Dilution reduces total particulate concentrations in the remote areas and predominantly determines the total deposited pollutant concentrations. Of these, pulmonary and nasopharyngeal deposition are most significant and, as a first approximation, correspond largely to the relative importance of the accumulation and dispersion modes of the sampled aerosol. A particle size distribution shift toward larger particles within the accumulation mode occurs upon ageing of the aerosol and reduces the pulmonary deposited fraction of the measured compounds in the background sites, compared to the one in the suburb. The total deposited fraction, however, increases. The contributions of biogenic higher odd n‐alkanes and, to a lesser extent, of even carboxylic acids to the dispersion mode of the aerosol result in an increased nasopharyngeal deposition at the background sites mainly during summer.

Since little information on the bio‐availability of organic aerosol constituents is available in the literature, the fractions of the particulate pollutant concentrations, resorbed in the tissues from the deposited material, were calculated, assuming an average efficiency of 70% for pulmonary and of 10% for nasopharyngeal and tracheobronchial resorption. A nearly constant total resorbed fraction of 20±2% resulted, independent of the sampling station or the season chosen, in contrast with the total deposited fractions, for which significant differences were observed. The predominant pulmonary resorption as well as compensating effects of the nasopharyngeal resorption level out the relatively small differences in particle size distributions observed. Based on these data, a first estimate in nanogram of the daily intake by inhalation of the organic pollutants studied can be formulated as four times the particulate pollutant concentration, expressed in ngm^‐3.     

Characteristics of mass distributions of aerosol particle and its inorganic water-soluble ions in summer over a suburb farmland in Beijing

Agricultural activity is one of the most important sources of aerosol particles. To understand the mass distribution and sources of aerosol particles and their inorganic water-soluble ions in a suburb farmland of Beijing, particle samples were collected using a microorifice uniform deposit impactor (MOUDI) in the summer of 2004 in a suburb vegetable field. The distribution of the particles and their inorganic water-soluble ions in the diameter range of 0.18–18 μm were measured. The dominant fine particle ions were SO₄ ^2?, NO₃ ^?, and NH₄ ⁺. The association of day-to-day variation of the concentration of these ions with temperature, humidity, and solar radiation suggested that they are formed by the reaction of NH₃ released from the vegetable field with the acid species produced from photochemical reactions. Fine particle K⁺ is likely from vegetation emission and biomass burning. Coarse particles like Ca²⁺, Mg²⁺, NO₃ ^?, and SO₄ ^2? are suggested to come from the mechanical process by which the soil particle entered the atmosphere, and from the reaction of the acid species at the surface of the soil particle. The results show that fertilizer and soil are important factors determining the aerosol particle over agricultural fields, and vegetable fields in suburban Beijing contribute significantly to the aerosol particle.     

Potential environmental impact of dissolution of raw phosphate in sea water of the Gulf of Aqaba

Dissolution of raw phosphate (apatite) in sea water of the Gulf of Aqaba was investigated through lab incubation experiments. Three types from three different sources (Al-Hasa, Al-Abyad and Esh-Shydiya) have been used for these experiments. Impact of quantity, grain size, and source (type) of raw phosphate on dissolution rate were studied. Statistical analysis shows significant differences between the results obtained from comparing each two weights; as weight of apatite increased, dissolved inorganic phosphate-phosphorus (DIP) and fluoride in sea water solution increased. The differences between the dissolution rates of raw phosphate from the three sites were not significant while the differences between the different grain size fractions were significant. Dissolution rates were inversely related to particle size. Using a worst-case scenario, a conservative estimate of the maximum increase in DIP in seawater of the Gulf of Aqaba due to the apatite particles lost to the sea during ship loading resulted in DIP concentrations of 0.03 μM per year. As the residence time of the water in the Gulf of Aqaba is about one year, the DIP concentration will not increase by more than 0.03 μM under the estimated annual quantity of exported phosphate. Fluoride will not increase by more than 0.03 mg/l under the same conditions.     

The use of δ18O as an indicator of vanadium movement in a dormant stratovolcano region

The oxygen isotope (δ¹⁸O) stable water tracer can be a promising new tool for identifying trace metals in volcanoes and their sources. In the present study, the origin of vanadium in water from a spring at the base of Mt. Fuji is examined using δ¹⁸O, a dormant stratovolcano consisting of lava and basalt rock located on the North Pacific Coast of Japan. A comparison of water from the main springs at the foot of the Mt. Fuji volcano indicates that only V, Cr, Mn and Co enrichment could be related to volcanic events, whereas Ni, Cu, Cd and Pb originate from the dissolution of particles of anthropogenic origin from the industrial areas of Fuji and Fujinomiya. The average V concentrations at the mountain sites ranged from 50 to 110 µg L^?1 and from 18 to 47 µg L^?1 in the coastal areas. The δ¹⁸O became depleted at higher elevations and increased in coastal areas as well as in some NO₃^?-contaminated water. Therefore, variations in the dissolved V/δ¹⁸O ratio in springs of the study area occur due to the elevations of their catchments and the increased concentrations of δ¹⁸O from NO₃^? as a contaminant.     

The importance of different forms of Pb on diminishing biological activities in a calcareous soil

In this experimental study, we evaluated the effect of different lead (Pb) fractions on biological properties in soil spiked with 0, 600, 1200 and 1800 mg kg^?1 Pb, during a 90-day incubation period at 25?28°C. Different Pb fractions were measured by sequential extraction at days 1 and 90 after soil treatment. Diethylenetriaminepentaacetic acid (DTPA)-extractable Pb and soil biological properties at days 1, 5, 15, 45 and 90 were measured. The concentration of Pb in soluble and exchangeable fractions was very high at day 1, but it showed remarkable transfer into carbonate and residual fractions by day 90. Substrate-induced respiration, basal respiration, acid and alkaline phosphatases, microbial populations (bacterial, fungal and actinomycetes) and biomass carbon decreased significantly with soil contamination compared with the control. With Pb ageing, these biological properties increased. Metabolic quotient (qCO₂) increased significantly compared with the control with increasing Pb concentration. The toxicity of various forms of Pb for the biological status of the soil was in the following order: KNO₃ extractable>NaOH extractable>EDTA extractable>HNO ₃ extractable>total content Pb. Thus, the bioavailable fractions are better indicators of Pb pollution in soils.     

Reproductive dynamics of the sea urchin Paracentrotus lividus on the Galicia coast (NW Spain): effects of habitat and population density

We studied the spatial variability in the size at first maturity and the reproductive cycle of Paracentrotus lividus in Galicia, contributing key information for the exploitation and management of this resource. The size at maturity varied between 20.4 (±1.2 SE) mm and 27.9 ± 1.2 mm and was smaller in areas of low population density where sea urchins do not form patches. Using a nonlinear model, we analysed the effect of depth, body size, sex and population density on the temporal pattern of the gonad index. The maximum and minimum indices were obtained at 4 m depth in the months before and after the spring spawning, respectively. The depth also affected the cycle phase, and the sea urchins at 4 m depth spawned 9.4 ± 3.0 days later than the sea urchins at 8 m depth and 20.5 ± 3.0 days later than those at 12 m depth. Moreover, the sea urchins living in patches showed a slight increase in gonad size as a consequence of the better-quality habitat. This shows that there is no intraspecific competition in this area despite the high population densities reached (18.5 kg m^?2).     

武汉市城区大气PM2．5的碳组分与源解析

大气细颗粒物（PM2．5）和碳组分（OC,EC）是影响大气能见度、气候变化以及人体健康的重要污染物,研究大气颗粒物及其中碳组分的污染特征及各类典型污染源对大气细颗粒物及碳组分的贡献,对于认识区域和城市大气污染状况,控制细颗粒物的污染,具有重要意义。2011年7月至2012年2月,利用大流量PM2．5采样器采集武汉市大气细颗粒物样品并对其碳组分进行测定。武汉市城区大气中PM215、OC和EC的质量浓度平均值分别为（127±48．7）、（19．4±10．5）和（2．9±1．48）μg·m-3。其PM2．5的浓度处于我国主要城市的中等偏高水平,而OC、EC的浓度则属中等偏下水平,但均高于国外城市。武汉市大气PM2,质量浓度的季节性变化呈现出秋季〉冬季〉夏季的趋势,是气象因素和污染源排放综合影响的结果。OC浓度和EC浓度具有较好的相关性（r2=0．69）,表明二者存在来源联系。OC／EC的比值为6．7,指示武汉市大气中OC和EC的来源受汽车尾气排放和生物质燃烧的共同影响。SOA的平均质量浓度值为12．5μg·m-3约占PM2．5平均质量浓度的9．8％,表明SOA对武汉市城区大气PM2．5具有重要贡献。结合PM2．5所含的水溶性离子、微量元素组成,利用正矩阵因子分析（PMF）模型对武汉市城区大气PM2．5来源进行解析,结果表明,其主要来源及贡献率分别为机动车源（27．1％）、二次硫酸盐和硝酸盐（26．8％）、工厂排放（26．4％）和生物质燃烧（19．6％）。