Safer alternatives assessment: the Massachusetts process as a model for state governments

In 2006 the Massachusetts Toxics Use Reduction Institute conducted a study to determine if states could identify safer alternatives to five chemicals of concern. The chemicals investigated included di (2-ethylhexyl) phthalate (DEHP), formaldehyde, hexavalent chromium, lead and perchloroethylene. First, the Institute developed a methodology for assessing alternatives to these five chemicals that allowed it to quickly determine priority uses and alternatives to assess and to research the pertinent decision criteria, which included performance, technical, financial environmental and human health parameters. The methodology included important feedback from stakeholders in the state, which helped to focus and enhance the value of the work. Second, the Institute implemented the methodology over a ten month period. Based on the activities conducted by the Institute, safer alternatives were identified for each of the priority uses associated with the five chemicals studied. This report summarizes the methodology employed and provides examples of the results for one of the five chemicals, namely DEHP. The experience of the Institute and the information contained in this report indicates that alternatives assessment was a useful approach to organizing and evaluating information about chemicals and alternatives.     

Sex in the beach: spermatophores, dermal insemination and 3D sperm ultrastructure of the aphallic mesopsammic Pontohedyle milaschewitchii (Acochlidia, Opisthobranchia, Gastropoda)

Sperm transfer via spermatophores is common among organisms living in mesopsammic environments, and is generally considered to be an evolutionary adaptation to reproductive constraints in this habitat. However, conclusions about adaptations and trends in insemination across all interstitial taxa cannot be certain as differences in mode of insemination via spermatophores do exist, details of insemination are lacking for many species, and evolutionary relationships in many cases are poorly known. Opisthobranch gastropods typically transfer sperm via reciprocal copulation, but many mesopsammic Acochlidia are aphallic and transfer sperm via spermatophores, supposedly combined with dermal fertilisation. The present study investigates structural and functional aspects of sperm transfer in the Mediterranean microhedylacean acochlid Pontohedyle milaschewitchii. We show that spermatophore attachment is imprecise. We describe the histology and ultrastructure of the two-layered spermatophore and discuss possible functions. Using DAPI staining of the (sperm-) nuclei, we document true dermal insemination in situ under the fluorescence microscope. Ultrastructural investigation and computer-based 3D reconstruction from TEM sections visualise the entire spermatozoon including the exceptionally elongate, screw-like keeled sperm nucleus. An acrosomal complex was not detected. From their special structure and behaviour we conclude that sperm penetrate epithelia, tissues and cells mechanically by drilling rather than lysis. Among opisthobranchs, dermal insemination is limited to mesopsammic acochlidian species. In this spatially limited environment, a rapid though imprecise and potentially harmful dermal insemination is discussed as a key evolutionary innovation that could have enabled the species diversification of microhedylacean acochlidians.     

Molecular Systematics and the Conservation of Rare Species

Abstract: Despite the tradition of systematic biology as the science of diversity, systematics has until recently contributed relatively little to the theory and practice of conservation biology. We identify four areas in which systematics could contribute to the conservation of rare plant species: (1) species concepts, (2) the identification of lineages worthy of conservation, (3) the setting of conservation priorities, and (4) the effects of hybridization on the biology and conservation of rare species. Species concepts that incorporate history and reflect phylogeny ultimately will be more useful for preserving biodiversity than those that do not. Phylogenetic analyses involving conspecific populations often reveal multiple lineages that may warrant protection as evolutionarily distinct units. Phylogenetic information also should be considered in setting priorities for conservation. Systematics provides the tools for inferring relationships among organisms and, in conjunction with biogeography, for identifying those areas that harbor many actively speciating groups. Hybridization may lead to the extinction of a rare species, but in other cases, ironically, artificial hybridization with a more widespread congener may be the only way to preserve the gene pool of a rare species. We appeal to systematists to contribute actively to both conservation theory and practice, and we call for the integration of systematics in the establishment of conservation priorities and the development of strategies to preserve Earth's biota.     

Ultra trace simultaneous determination of 50 polycyclic aromatic hydrocarbons in biota using pMRM GC-MS/MS

Abstract

A saponification extraction method with gas chromatography pseudo-MRM (pMRM) mass spectrometry detection was developed for the determination of 50 total polycyclic aromatic hydrocarbons (TPAH50, a combination of parent and alkylated homologues) in biota. The method was aimed at monitoring and identification of potential TPAH contaminants in bitumen impacted environments. Alkylated PAHs were determined by multi-level, quantitative calibration using parent PAHs. The developed and thoroughly validated method required only one injection for TPAH50 analysis which represents significant saving of time and expensive authentic alkylated standards. The current method was tested with certified reference mussel tissue NIST 1974c and performed well. In a comparison study, the method reached a limit of quantitation (LOQ) for the TPAH50 between 0.1 and 0.2?ng g^?1, while the QuEChERs enhanced matrix removal – lipid (EMR) kit produced by Agilent showed an LOQ of 5–10?ng g^?1. The current method relied on response factors (RF) for the quantitation of alkylated PAHs determined against parent PAHs. These RFs were shown to be stable and consistent over the course of 1 year, during which over 200 routine environmental biota monitoring samples were analyzed. The environmental biota monitoring samples analyzed include muscle, carcass and liver, with an average total PAH50 concentration of 13, 90 and 135?ng g^?1, respectively. Results show significant differences in the distributions of 1 ringed, 2 ringed, 3 ringed, 4 ringed, and 5+ ringed TPAHs between the types of biota samples.     

Determination of lindane leachability in soil-biosolid systems and its bioavailability in wheat plants

The leachability of lindane from different biosolid amended soils was determined and compared to its bioavailability. Sand, soil, and a mixture of soil-sand (1:1 w/w) were spiked with lindane, blended with different amounts of biosolids, and subjected to a leaching process with water that lasted for 1-28 d. This procedure is in accordance with ISO/TS 21268-1: 2007. After these batch tests, lindane was extracted from the leachates using three different solvent-free microextraction techniques, including solid phase microextraction (SPME), stir-bar sorptive extraction (SBSE), and silicone rod extraction (SRE). The amount of lindane was determined with thermal desorption and gas chromatography coupled to mass spectrometry (GC-MS). The efficiencies of the three microextraction techniques were statistically different, and the efficiency could be related to the amount of polydimethylsiloxane (PDMS) in each extraction device. However, all of the techniques provide data that shows that the leachability of lindane is dependent on the amount of organic matter contained in the matrix.The results of the lindane leachability assay were compared to the bioavailability of lindane, which was determined by measuring the amount of lindane that accumulated in the roots of wheat plants grown in similar soil-biosolid systems.It was confirmed that the amount of organic matter in the matrix is a determining factor for lindane immobilization. The presence of biosolids decreases the mobility of lindane in all of the systems under study. Similarly, increasing biosolid concentrations in the soil significantly decreased the bioavailability of lindane and, consequently, plant absorption.The good correlation (R² = 0.997) between the leachability of lindane from the matrix and plant absorption of lindane indicates that the proposed biomimetic methodology can predict the bioavailability of lindane in a time period as short as 7 d.The results of this work confirm that amending contaminated soils with biosolids is beneficial for immobilizing lindane and helps prevent the percolation of lindane through the soil profile and into groundwater.     

Chlorinated Solvents: Will the Alternatives be Safer?

Over the next decade, use of chlorinated solvents, a widely employed class of chemicals, will decline significantly because of increasingly stringent environmental regulations. These solvents pose certain health and environmental problems and they have been heavily scrutinized. The alternatives to the solvents are being adopted without controls. In some cases, these substances will pose other health and environmental problems that are likely to be as serious; in other cases, the alternatives have not been examined for their health and environmental effects at all. This case study demonstrates that regulations on chlorinated solvents and their potential alternatives are inconsistent with one another and conflicting.     

Control of Fine Particulate (PM2.5) Emissions from Restaurant Operations

ABSTRACT

This paper describes efforts to reduce particulate matter (PM) emissions from restaurant operations, including application of an existing control method to a new equipment type. Commercial charbroiling in the South Coast Air Basin results in emissions of approximately 10 tons/day of fine particulate matter ₍PM_2.5) and 1.3 tons/day of volatile organic compounds (VOCs). Over a seven-year period, the South Coast Air Quality Management District worked with industry to develop test methods for measuring emissions from various cooking operations, evaluate control technologies, and develop a rule to reduce these emissions.

Of the two basic types of charbroilers—chain-driven and underfired—underfired produce four times the emissions when equivalent amounts of product are cooked. Cost-effective control technology is currently available only for chain-driven charbroilers. The application of flameless catalytic oxidizers to chain-driven charbroilers was found to effectively reduce emissions by at least 83% and is cost-effective. The catalysts have been used worldwide at restaurants for several years. Research efforts are underway to identify control options for underfired charbroilers.

Implementation of Rule 1138, Control of Emissions from Restaurant Operations, adopted November 14, 1997, will result in reductions of 0.5 tons/day of PM_2.5 and 0.2 tons/day of VOCs. Future rules will result in reductions from underfired charbroilers and possibly other restaurant equipment when cost-effective solutions are available.     

Evidence of nuclear reactions in the Pd lattice

An operating Pd//D₂O, Li⁺, Cl⁻//Pt cell, placed in an external electrostatic field, yielded unexpected results, viz. (i) Morphological changes in the form of discrete sites exhibiting molten-like features, i.e. features that require substantial energy expenditure. (ii) Presence of elements (Al, Mg, Ca, Si, Zn, ...) that could not be extracted from cell components and deposited on discrete sites. The cell design and the experimental protocol assuring reproducibility is described in detail.     

Consistency of ozone and nitrogen oxides standards at tropospherically relevant mixing ratios

The absolute accuracy and long-term precision of atmospheric measurements hinge on the quality of the instrumentation and calibration standards. To assess the consistency of the ozone (O3) and nitrogen oxides (NO(x)) standards maintained at the National Institute of Standards and Technology (NIST), these standards were compared through the gas-phase titration of O3 with nitric oxide (NO). NO and O3 were monitored using chemiluminescence and UV absorption, respectively. Nitrogen dioxide (NO2) was monitored directly by laser-induced fluorescence and indirectly by catalytic conversion to NO, followed by chemiluminescence. The observed equivalent loss of both NO and O3 and the formation of NO2 in these experiments was within 1% on average over the range of 40-200 nmol mol(-1) of NO in excess O3, indicating that these instruments, when calibrated with the NIST O3 and NO standards and the NO2 permeation calibration system, are consistent to within 1% at tropospherically relevant mixing ratios of O3. Experiments conducted at higher initial NO mixing ratios or in excess NO are not in as good agreement. The largest discrepancies are associated with the chemiluminescence measurements. These results indicate the presence of systematic biases under these specific conditions. Prospects for improving these experiments are discussed.