Urban metabolism refers to the assessment of the amount of resources produced and consumed by urban ecosystems. It has become an important tool to understand how the development of one city causes impacts to the local and regional environment and to support a more sustainable urban design and planning. Therefore, the purpose of this paper was to measure the changes in material and energy use occurred in the city of Curitiba (Brazil) between the years of 2000 and 2010. Results reveal better living conditions and socioeconomic improvements derived from higher resource throughput but without complete disregard to environmental issues. Food intake, water consumption and air emissions remained at similar levels; energy use, construction materials and recycled waste were increased. The paper helps illustrate why it seems more adequate to assess the contribution a city makes to sustainable development than to evaluate if one single city is sustainable or not.

PM2.5 concentrations in a typical residential apartment in Beijing and immediately outside of the building were measured simultaneously during heating and non-heating periods. The objective was to quantitatively explore the relationship between indoor and outdoor PM2.5 concentrations. A statistical method for predicting indoor PM2.5 concentrations was proposed. Ambient PM2.5 concentrations were strongly affected by meteorological conditions, especially wind directions. A bimodal distribution was identified during the heating season due to the frequent and rapid transition between severe pollution events and clean days. Indoor PM2.5 concentrations were significantly correlated with outdoor PM2.5 concentrations but with 1–2 h delay, and the differences can be explained by ambient meteorological features, such as temperature, humidity, and wind direction. These results indicate the potential to incorporate indoor exposure features to the regional air quality model framework and to more accurately estimate the epidemiological relationship between human mortality and air pollution exposure.

This study provides the first estimate of dry deposition fluxes of criteria air pollutants (SO2 and NOx) across the Three Northern Regions Shelter Forest (TNRSF) region in Northern China and their long-term trends from 1982 to 2010 using the inferential method. Dry deposition velocities of SO2 and NOx increased in many places of the TNRSF up to 118.2% for SO2 and 112.1% for NOx over the last three decades due to the increased vegetation coverage over the TNRSF. The highest atmospheric deposition fluxes of SO2 and NOx were found in the Central-North China region, followed by the Northeast and the Northwest China regions of the TNRSF. A total of 820,000 t SO2 and 218,000 t NOx was estimated to be removed from the atmosphere through dry deposition process over the TNRSF from 1982 to 2010. About 50% of the total removal occurred in the Central-North China region. The estimated total SO2 and NOx dry deposition fluxes from 1982 to 2010 between a TNRSF site in this region and an adjacent farmland outside the TNRSF showed that the fluxes of these two chemicals at the TNRSF site were the factors of 2–3 greater than their fluxes in the farmland.

A combination of in vitro and in vivo studies on tomato (Lycopersicon esculentum Mill. cv. Triton) revealed that environmentally-relevant levels of ozone (O3) pollution adversely affected pollen germination, germ tube growth and pollen-stigma interactions – pollen originating from plants raised in charcoal-Purafil® filtered air (CFA) exhibited reduced germ tube development on the stigma of plants exposed to environmentally-relevant levels of O3. The O3-induced decline in in vivo pollen viability was reflected in increased numbers of non-fertilized and fertilized non-viable ovules in immature fruit. Negative effects of O3 on fertilization occurred regardless of the timing of exposure, with reductions in ovule viability evident in O3 × CFA and CFA × O3 crossed plants. This suggests O3-induced reductions in fertilization were associated with reduced pollen viability and/or ovule development. Fruit born on trusses independently exposed to 100 nmol mol−1 O3 (10 h d−1) from flowering exhibited a decline in seed number and this was reflected in a marked decline in the weight and size of individual fruit – a clear demonstration of the direct consequence of the effects of the pollutant on reproductive processes. Ozone exposure also resulted in shifts in the starch and ascorbic acid (Vitamin C) content of fruit that were consistent with accelerated ripening. The findings of this study draw attention to the need for greater consideration of, and possibly the adoption of weightings for the direct impacts of O3, and potentially other gaseous pollutants, on reproductive biology during ‘risk assessment’ exercises.

Pollution adversely affects vegetation; however, its impact on phenology and leaf morphology is not satisfactorily understood yet. We analyzed associations between pollutants and phenological data of birch, hazel and horse chestnut in Munich (2010) along with the suitability of leaf morphological parameters of birch for monitoring air pollution using two datasets: cumulated atmospheric concentrations of nitrogen dioxide and ozone derived from passive sampling (short-term exposure) and pollutant information derived from Land Use Regression models (long-term exposure). Partial correlations and stepwise regressions revealed that increased ozone (birch, horse chestnut), NO2, NOx and PM levels (hazel) were significantly related to delays in phenology. Correlations were especially high when rural sites were excluded suggesting a better estimation of long-term within-city pollution. In situ measurements of foliar characteristics of birch were not suitable for bio-monitoring pollution. Inconsistencies between long- and short-term exposure effects suggest some caution when interpreting short-term data collected within field studies.

We tested seven contemporary agrochemicals as potential plant protectants against ozone phytotoxicity. In nine experiments, Bel-W3 tobacco plants were experienced weekly exposures to a) 80 nmol mol−1 of ozone-enriched or ozone-free air in controlled environment chambers, b) an urban air polluted area, and c) an agricultural-remote area. Ozone caused severe leaf injury, reduced chlorophylls' and total carotenoids' content, and negatively affected photosynthesis and stomatal conductance. Penconazole, (35% ± 8) hexaconazole (28% ± 5) and kresoxim-methyl (28% ± 15) showed higher plants’ protection (expressed as percentage; mean ± s.e.) against ozone, although the latter exhibited a high variability. Azoxystrobin (21% ± 15) showed lower protection efficacy and Benomyl (15% ± 9) even lower. Trifloxystrobin (7% ± 11) did not protect the plants at all. Acibenzolar-S-methyl + metalaxyl-M (Bion MX) (−6% ± 17) exhibited the higher variability and contrasting results: in some experiments it showed some protection while in others it intensified the ozone injury by causing phytotoxic symptoms on leaves, even in control plants.

A two-year experiment exposing Acer truncatum Bunge seedlings to elevated ozone (O3) concentrations above ambient air (AO) and drought stress (DS) was carried out using open-top chambers (OTCs) in a suburb of Beijing in north China in 2012–2013. The results suggested that AO and DS had both significantly reduced leaf mass area (LMA), stomatal conductance (Gs), light saturated photosynthetic rate (Asat) as well as above and below ground biomass at the end of the experiment. It appeared that while drought stress mitigated the expression of foliar injury, LMA, leaf photosynthetic pigments, height growth and basal diameter, due to limited carbon fixation, the O3 – induced reductions in Asat, Gs and total biomass were enhanced 23.7%. 15.5% and 8.1% respectively. These data suggest that when the whole plant was considered that drought under the conditions of this experiment did not protect the Shantung maple seedlings from the effects of O3.

Levels of polybrominated diphenyl ethers (PBDEs) and dechlorane plus (DPs) were investigated in the Indus River Basin from Pakistan. Concentrations of ∑PBDEs and ∑DPs were ranged between 0.05 and 2.38 and 0.002–0.53 ng g−1 in the surface soils while 1.43–22.1 and 0.19–7.59 pg m−3 in the passive air samples, respectively. Black carbon (fBC) and total organic carbon (fTOC) fractions were also measured and ranged between 0.73 and 1.75 and 0.04–0.2%, respectively. The statistical analysis revealed strong influence of fBC than fTOC on the distribution of PBDEs and DPs in the Indus River Basin soils. BDE's congener profile suggested the input of penta–bromodiphenylether (DE-71) commercial formulation in the study area. Soil–air partitioning of PBDEs were investigated by employing octanol-air partition coefficients (KOA) and black carbon-air partition coefficients (KBC−A). The results of both models suggested the combined influence of total organic carbon (absorption) and black carbon (adsorption) in the studied area.

Lichens, symbioses of fungi and algae and/or cyanobacteria, have the remarkable ability to uptake and accumulate semivolatile organic compounds (SVOC) from air, including polycyclic aromatic hydrocarbons (PAHs), but the mechanism of accumulation is still unknown. Understanding these mechanisms is critical to standardize the use of lichens as environmental bioindicators and to further integrate them in air monitoring networks. Through a series of experiments we show that gas phase PAHs easily cross lichen's surface and accumulate in the photosynthetic algal layer of lichens. Once accumulated, they remain in the algal layer and not within the fungus hyphae, or adhered to lichen's surface, as it was previously supposed to happen. Additionally, when lichens are washed, gas phase PAHs still remain in the algal layer. Our results reveal that lichens may be utilized as bioindicators of gas phase PAHs, overcoming current limitations of air monitoring.

Following the ban of polybrominated diphenyl ethers, other halogenated flame retardants (FRs) might be used increasingly. This study has analyzed hexabromocyclododecane (HBCD), 1,2-bis(2,4,6-tribromophenoxy)-ethane (BTBPE), 2,3-dibromopropyl-2,4,6-tribromophenyl ether (DPTE) and dechlorane plus (DP) in Greenland air over the course of a year. Moreover, BTBPE, DPTE, DP, 2-ethylhexyl-2,3,4,5-tetrabromobenzoate (TBB), bis(2-ethylhexyl)tetrabromophthalate (TBPH) and decabromodiphenyl ethane (DBDPE) were analyzed in samples of polar bear, ringed seal, black guillemot and glaucous gull from Greenland. HBCD in air appeared low, while mean concentrations of syn- and anti-DP were 2.3 and 5.2 pg/m3, respectively. BTBPE and DPTE were undetectable in air. Detection frequencies in biota were <50% for BTBPE, TBPH and DBDPE, but near 100% for the remaining compounds. Ringed seals from East Greenland had highest mean concentrations of TBB, DPTE, syn- and anti-DP (1.02, 0.078, 0.096 and 0.42 ng/g wet weight, respectively). Our study documents the long-range transport and, to some extent, bioaccumulation of these novel FRs.