A Survey of Ambient Air Levels of Lead in El Paso,Texas from 1972–1979

In an era when the cost of compliance with state and federal environmental laws is rapidly rising, sometimes entities, such as operators of waste sites, are unable to pay these and other operating costs and are forced to file for bankruptcy. Citing Midlantic Nat'l Bank v. N.J. Dep't of Envtl. Protection and state environmental laws, bankruptcy trustees may be suing PRPs in bankruptcy courts to share the costs to clean up debtors' waste sites. This article suggests strategies by which PRPs can avoid litigating such lawsuits in the bankruptcy courts and instead resolve them before state and/or federal forums—where they properly belong.     

Accounting for carbon stocks in models of land-use change: an application to Southern Yucatan

To assess the impact of land-use change on carbon stocks, we apply a new methodology, linking ecological and economic modeling, to southern Yucatan, Mexico. A spatial econometric multinomial logit model of ten land-cover classes is estimated (four primary forest categories, three secondary growth categories, an invasive species, and two agricultural land-cover categories), using satellite data on land cover, linked with census socioeconomic data and other biophysical spatial data from 2000. The analysis is novel in that it is the first attempt to link detailed satellite data on land use, with on-the-ground estimates of carbon stocks in a spatial econometric model of land use. The estimated multinomial logit model is then used with two scenarios of future economic growth (“low growth” and “high growth” changes in population, agricultural land use, market access, and education levels) in the region to predict land-cover changes resulting from the economic growth. The per hectare carbon (C) stocks in each land-cover class are derived from previously published estimates of biomass from field sampling across the study region. We consider aboveground-only, aboveground plus soil, transient and non-transient pools of carbon. These estimates are scaled up to the total area in each class according to the predictions of the model baseline and the two development scenarios. Subsequently, the changes in carbon stocks resulting from the predicted land-cover changes are calculated. Under the low growth scenario, carbon stocks declined by 5%; under the high growth scenario, losses were 12%. Including soil C, the proportional losses were lower, but the absolute amount lost was more than double (to 6 Tg C under the low and almost 15 Tg C under the high-growth scenario). This methodology could be further developed for applications in global change policy, such as payments for environmental services (PES) or reduction in emissions from deforestation and degradation (REDD).     

Global Emission Ceiling Versus International Cap and Trade: What is the Most Efficient System to Solve the Climate Change Issue?

We model the climate change issue as a pollution control game with the purpose of comparing two possible departures from the business as usual (BAU) where countries noncooperatively choose their emission levels. In the first scenario, players have to agree on a global emission cap (GEC) that is enforced by a uniform taxation scheme. They still behave strategically when choosing emission levels but are now subject to the coupled constraint imposed by the cap. The second scenario consists of the implementation of an international cap and trade (ICT) system. In this case, players decide on their emission quotas, and emission trading is allowed. A three heterogenous player quadratic game serves as a basis for the analysis. When the cap is binding, among all the coupled constraints Nash equilibria, we select a particular normalized equilibrium by solving a variational inequality. Comparing the normalized equilibrium with the Nash equilibria of the BAU and the ICT, we first show that if the cap is appropriately chosen, then the GEC system improves all players’ payoffs, relative to the BAU. The GEC system may thus be unanimously approved whereas the ICT is not, because moving from the BAU to the ICT is costly for one player. Second, for some values of the cap, all players get a higher payoff under the GEC than under the ICT. Therefore, the GEC outperforms the ICT both in terms of feasibility and efficiency.     

Coupling occurs before breakdown during biotransformation of Acid Blue 62 by white rot fungi

Only few data exist on the metabolites produced during the biotransformation of anthraquinonic dyes by white rot fungi (WRF). During the biotransformation of an anthraquinonic dye Acid Blue 62 (ABu62) using Pycnoporus sanguineus MUCL 41582 strain, it was previously demonstrated that the blue colour of the medium turned to red before complete dye decolourisation. To better understand the phenomenon, this study carried out ABu62 biotransformation with five different WRF strains (Coriolopsis polyzona MUCL 38443, Perenniporia ochroleuca MUCL 41114, Perenniporia tephropora MUCL 41562, P. sanguineus MUCL 38531 and Trametes versicolor MUCL 38412) and compared with P. sanguineus MUCL 41582 previously described. A multi-methodological approach (using capillary electrophoresis, mass spectrometry, HPLC, UV, NMR and IR spectroscopies) was developed to characterise the metabolites involved and monitor their apparition. Seven metabolites were commonly found with all strains, suggesting a common metabolic pathway for ABu62 biotransformation. During the first days, dimer and oligomers of the initial ABu62 molecule were observed: the main one absorbed in the 500nm region, explaining the red colour appearance of the medium. This main metabolite was made up of two molecules of ABu62 linked by an azo bond, minus a cyclohexyl moiety. After a longer incubation time, breakdown products were observed. Based on these products characterizations, a bioconversion pathway was proposed.     

Hemocyte-specific responses to the peroxidizing herbicide fomesafen in the pond snail Lymnaea stagnalis (Gastropoda, Pulmonata)

Responses of circulating hemocytes were studied in Lymnaea stagnalis exposed to 10, 30, 90, and 270 microg/L fomesafen for 24 and 504 h. Flow cytometry was used to quantify fomesafen-induced production of reactive oxygen species (ROS), phagocytic activity on Escherichia coli, and oxidative burst when hemocytes were challenged by E. coli or phorbol 12-myristate-13-acetate (PMA). Lysosomal membrane damage was assessed, using the neutral-red retention time (NRRT) assay. Exposure to fomesafen for 24 h resulted in increase in ROS levels and decreases in phagocytosis and the oxidative burst in PMA-stimulated hemocytes. After 504 h, intracellular levels of ROS returned to normal, but phagocytosis of E. coli was still inhibited and the associated oxidative burst significantly reduced. After both durations of exposure, decreases of NRRT indicated that lysosome membrane fragility increased with fomesafen concentration. Potential implications for the health and survival of the snails and consequences on populations are discussed.     

Realising a resilient and sustainable built environment: towards a strategic agenda for the United Kingdom

Recent natural and human-induced emergencies have highlighted the vulnerability of the built environment. Although most emergency events are not entirely unexpected, and the effects can be mitigated, emergency managers in the United Kingdom have not played a sufficiently proactive role in the mitigation of such events. If a resilient and sustainable built environment is to be achieved, emergency management should be more proactive and receive greater input from the stakeholders responsible for the planning, design, construction and operation of the built environment. This paper highlights the need for emergency management to take a more systematic approach to hazard mitigation by integrating more with professions from the construction sector. In particular, design changes may have to be considered, critical infrastructures must be protected, planning policies should be reviewed, and resilient and sustainable agendas adopted by all stakeholders.     

Measurements of stem diameter: implications for individual- and stand-level errors

Stem diameter is one of the most common measurements made to assess the growth of woody vegetation, and the commercial and environmental benefits that it provides (e.g. wood or biomass products, carbon sequestration, landscape remediation). Yet inconsistency in its measurement is a continuing source of error in estimates of stand-scale measures such as basal area, biomass, and volume. Here we assessed errors in stem diameter measurement through repeated measurements of individual trees and shrubs of varying size and form (i.e. single- and multi-stemmed) across a range of contrasting stands, from complex mixed-species plantings to commercial single-species plantations. We compared a standard diameter tape with a Stepped Diameter Gauge (SDG) for time efficiency and measurement error. Measurement errors in diameter were slightly (but significantly) influenced by size and form of the tree or shrub, and stem height at which the measurement was made. Compared to standard tape measurement, the mean systematic error with SDG measurement was only ?0.17 cm, but varied between ?0.10 and ?0.52 cm. Similarly, random error was relatively large, with standard deviations (and percentage coefficients of variation) averaging only 0.36 cm (and 3.8%), but varying between 0.14 and 0.61 cm (and 1.9 and 7.1%). However, at the stand scale, sampling errors (i.e. how well individual trees or shrubs selected for measurement of diameter represented the true stand population in terms of the average and distribution of diameter) generally had at least a tenfold greater influence on random errors in basal area estimates than errors in diameter measurements. This supports the use of diameter measurement tools that have high efficiency, such as the SDG. Use of the SDG almost halved the time required for measurements compared to the diameter tape. Based on these findings, recommendations include the following: (i) use of a tape to maximise accuracy when developing allometric models, or when monitoring relatively small changes in permanent sample plots (e.g. National Forest Inventories), noting that care is required in irregular-shaped, large-single-stemmed individuals, and (ii) use of a SDG to maximise efficiency when using inventory methods to assess basal area, and hence biomass or wood volume, at the stand scale (i.e. in studies of impacts of management or site quality) where there are budgetary constraints, noting the importance of sufficient sample sizes to ensure that the population sampled represents the true population.     

Scouts behave as streakers in honeybee swarms

Harmonic radar tracking was used to record the flights of scout bees during takeoff and initial flight path of two honeybee swarms. One swarm remained intact and performed a full flight to a destination beyond the range of the harmonic radar, while a second swarm disintegrated within the range of the radar and most of the bees returned to the queen. The initial stretch of the full flight is characterized by accelerating speed, whereas the disintegrating swarm flew steadily at low speed. The two scouts in the swarm displaying full flight performed characteristic flight maneuvers. They flew at high speed when traveling in the direction of their destination and slowed down or returned over short stretches at low speed. Scouts in the disintegrating swarm did not exhibit the same kind of characteristic flight performance. Our data support the streaker bee hypothesis proposing that scout bees guide the swarm by traveling at high speed in the direction of the new nest site for short stretches of flight and slowing down when reversing flight direction.     

Buffer sensitivity of photosynthetic carbon utilisation in eight tropical seagrasses

Some of the mechanisms involved in inorganic carbon (Ci) acquisition by tropical seagrasses from the western Indian Ocean were described by Björk et al. (Mar Biol 129:363–366, 1997). However, since then, it has been found that an additional, buffer-sensitive, system of Ci utilisation may operate in some temperate seagrasses (Hellblom et al. in Aquat Bot 69:55–62, 2001, Hellblom and Axelsson in Photos Res 77:173–191, 2003); this buffer sensitivity indicates a mechanism in which electrogenic H⁺ extrusion may form acidic diffusion boundary layers, in which either HCO ₃ ^? –H⁺ is co-transported into the cells, or where HCO ₃ ^? is converted to CO₂ (as catalysed by carbonic anhydrase) prior to uptake of the latter Ci form. Because a buffer was used in the 1997 study, we found it important to reinvestigate those same eight species, taking into account the direct effect of buffers on this potential mode of Ci acquisition in these plants. In doing so, it was found that all seagrass species investigated except Cymodocea serrulata were sensitive to 50 mM TRIS buffer of the same pH as the natural seawater in which they grew (pH 8.0). Especially sensitive were Halophila ovalis, Halodule wrightii and Cymodocea rotundata, which grow high up in the intertidal zone (only ca. 50–65% of the net photosynthetic activity remained after the buffer additions), followed by the submerged Enhalus acoroides and Syringodium isoetifolium (ca. 75% activity remaining), while Thalassia hemprichii and Thalassodendron ciliatum, which grow in-between the two zones, were less sensitive to buffer additions (ca. 80–85% activity remaining). In addition to buffer sensitivity, all species were also sensitive to acetazolamide (AZ, an inhibitor of extracellular carbonic anhydrase activity) such that ca. 45–80% (but 90% for H. ovalis) of the net photosynthetic activity remained after adding this inhibitor. Raising the pH to 8.8 (in the presence of AZ) drastically reduced net photosynthetic rates (0–14% remaining in all species); it is assumed that this reduction in rates was due to the decreased CO₂ concentration at the higher pH. These results indicate that part of the 1997 results for the same species were due to a buffer effect on net photosynthesis. Based on the present results, it is concluded that (1) photosynthetic Ci acquisition in six of the eight investigated species is based on carbonic anhydrase catalysed HCO ₃ ^? to CO₂ conversions within an acidified diffusion boundary layer, (2) C. serrulata appears to support its photosynthesis by extracellular carbonic anhydrase catalysed CO₂ formation from HCO ₃ ^? without the need for acidic zones, (3) H. ovalis features a system in which H⁺ extrusion may be followed by HCO ₃ ^? –H⁺ co-transport into the cells, and (4) direct, non-H⁺-mediated, uptake of HCO ₃ ^? is improbable for any of the species.