Search

Eggs of double-crested and pelagic cormorants were collected between 1973 and 1998 from colonies in the Strait of Georgia, BC, Canada, and assayed for concentrations of polychlorinated dibenzo-p-dioxins (PCDDs), dibenzofurans (PCDFs), and non-ortho- and mono-ortho-biphenyls (PCBs). Double-crested cormorant eggs contained (on average) up to 433 ng kg(-1) wet weight 1,2,3,6,7,8-HxCDD, 151 ng kg(-1) 1,2,3,7,8-PnCDD, and 74 ng kg(-1) 2,3,7,8-TCDD, whereas pelagic cormorant eggs contained up to 300, 99, and 28 ng kg(-1) wet weight of these respective congeners. The dominant non-ortho-PCB was CB-126, which ranged as high as 2263 ng kg(-1) in double-crested cormorant eggs. Concentrations of PCDDs and PCDFs fell dramatically in the early 1990s, following both severe restrictions on the use of chlorophenolic wood preservatives and antisapstains and a switch from molecular chlorine bleaching to alternative bleaching technologies at pulp mills in the region. Concentrations of PCBs did not show similar marked declines over time. On the basis of total TEQs > or = 148 ng kg(-1) and previously published documentation of effects in siblings of the cormorant eggs analyzed here, double-crested cormorant young may have exhibited significantly elevated EROD activity and/or brain asymmetries at all colonies from 1973 to 1989 and even at some colonies during the 1990s. Pelagic cormorant eggs collected from a few colonies in 1988-1989 also contained total TEQs greater than the threshold value estimated for double-crested cormorants.

The optimization of supercritical fluid extraction using CO2 for the extraction of contaminants in 15 samples of recycled paper and board (P&B) has been studied. An experimental design was used for simultaneous optimization of the variables involved in both the extraction step and the collection of the extract. Methanol was used as modifier. Several plastisizers such as diethyl phthalate, diisobutyl phthalate, di-n-butyl phthalate, dioctyl adipate, and diethylhexyl phthalate (from 2 to 100 microg/g of paper) were found in the recycled P&B samples. A discriminate analysis applied to all results obtained allow us to classify the samples in three different groups according to the content of recycled pulp (0, 10-30, and > 80% of recycled pulp), the sample thickness (from 600 microm), and the surface treatment of the paper. The analytical behavior and the results are discussed.

Examination of historical data shows that 3.5 x 10(8) tonnes (t) of residential refuse was discarded in New York City (NYC) during the 20th century. Maximum and minimum rates of per capita mass discard of residential refuse during this time are reported in 1940 (940 kg per capita yr(-1)) and 1961, 1963 (320 kg per capita yr(-1)), respectively. Since 1980, per capita residential refuse discard rates have been steady and comparatively low (430 kg per capita yr(-1) +/- 2.5%). Fuel ash accounted for approximately 34% of residential refuse in NYC during the century. A decline of refuse bulk density (as collected) from approximately 500 to 200 kg m(-3) and an increase in refuse organic matter content from 20% to 80% (by mass) is reported between 1920 and 1990 and is due largely to mass fraction reductions forfuel ash and increases for paper and plastic. Approximately 4.9 x 10(8) t of refuse was disposed in NYC during the 20th century (including commercial and residential refuse), representing a total pool of about 8.0 x 10(7) t of organic carbon (as C) that has entered city landfills and incinerators.

Mill process changes and source controls instituted in the late 1980s at pulp and paper mills along the British Columbia (BC) coast produced dramatic reductions in both the concentrations of polychlorinated dibenzo-p-dioxins and dibenzofurans (PCDD/Fs) and the TEQ (2,3,7,8-TCDD toxic equivalents). Nevertheless, questions remained as to whether the sediments were acting as contaminant sources or sinks, whether crab uptake pathways have stayed the same since the mills ceased producing PCDD/Fs, and whether improvement was faster at some sites than others. To examine the processes governing the changes in PCDD/F composition, PCDD/F sources and compositional trends for the coastal BC sites were interpreted using sediment and crab PCA (principal components analysis) models and two indices based on the three main groups of PCDD/Fs that covary in all PCA models. One index measured the relative inputs of chlorine bleaching PCDFs and PCP (pentachlorophenol)-related PCDDs at each mill and harbor site whereas the other measured the relative inputs of PCP wood preservatives and pulp mill effluents. Results indicated that PCDFs produced during chlorine bleaching accumulate from sediments to crabs more readily than the PCDDs but that the chlorine bleaching TCDFs have generally decreased in importance at all mill sites. In the years just before 1995, little change was observed in either the proportion of toxic 2,3,7,8-chlorinated congeners or the PCDD/F concentrations, and the improvements seemed to have largely ceased by 1995. The lack of change in PCA composition for the harbors provided a further, disturbing indication that ecosystem recovery may have stalled. Results also implied that the main route of PCDD/Fs into crabs shifted from uptake via a pelagic food web incorporating effluent-borne PCDD/Fs associated with suspended particulate matter to uptake via a benthic food web.

Drinking water is supplied by individual roof-catchment systems for homes and businesses near a dissolving sulfite pulp mill (now closed) located just north of Ketchikan in southeast Alaska. This study was conducted to determine if polychlorinated dibenzo-p-dioxins and polychlorinated dibenzofurans (PCDDs/Fs) found in the sediments of the roof-catchment cisterns resulted from historical deposition of stack emissions from the pulp mill's multi-fuel power boilers. Fly ash from the power boilers had maximum total PCDD/F concentrations of 3.08 x 10(5)-3.10 x 10(6) ng/kg, which resulted from combustion of bleach plant wastewater sludge and saltwater-soaked wood waste. Cistern sediments had maximum total PCDD/F concentrations of 7.71 x 10(4) ng/kg. Potential sources of PCDDs/Fs in the cistern sediments were considered to be automobile exhaust, heating oil combustion, and private trash burning as well as pulp mill boiler emissions. Discriminant analysis was used to analyze differences between profiles of tetra through octa homologue classes of PCDDs/ Fs (defined as proportional contributions to total concentration) from different source terms. Homologue profiles of potential sources from Ketchikan included in this analysis were fly ash collected from the mill's power boilers and soils collected from background areas (areas with similar PCDD/F sources as the residences [e.g., auto exhaust and burn barrels] near the mill but beyond the zone of aerial deposition of emissions from the mill). Profiles for emissions from automobile exhaust, fertilizers, oil heating, residential trash burning, and residential wood heating were also included in the source "training" data set (for the discriminant analysis) using data from published literature. The classification rules developed from the discriminant analysis were applied to the following test media sampled at Ketchikan: roof-catchment cistern sediments and soils collected from areas in the vicinity of the mill's power boilers (i.e., nearby residential or commercial [developed] areas, on the mill property, and nearby forestlands). The homologue profiles of cistern sediment and nearby developed area soil samples were similar to background soils, whereas the profiles for the forestland soil samples (influenced by emissions from the mill but not other anthropogenic sources) closely matched the fly ash pattern. The homologue profiles of the emission sources from published data were more similar to one another than either background soils or fly ash. Soil samples from the mill property were classified as members of all source groups. On the basis of these analyses, the composition of PCDDs/Fs detected in the cistern sediments is typical of Ketchikan background conditions and not reflective of mill emissions.

Fluorescence excitation-emission matrix (EEM) spectrophotometry was applied to five neighboring rivers, including one that is impacted by wastewater from a large tissue mill, to determine if fluorescence spectrophotometry could be used to differentiate between the river waters. River water samples from both the tissue mill effluent and the impacted river, the Park Burn, exhibited significantly higher fluorescence intensity than the other sites. This fluorescence was dominated by tryptophan fluorescence and a fluorescence center possibly due to the presence of fluorescent whitening agents. In contrast, the three other rivers exhibited lower fluorescence intensities typical of river systems with tryptophan (sewage), humic-like (peat derived color), and fulvic-like (natural organic matter) sources. It is suggested that fluorescence EEM spectrophotometry has the potential to provide a useful tool for pollution detection, monitoring, and control of paper industry impacts on river systems.

We report a method, based on the principles of origami (paper folding), for fabricating three-dimensional (3-D) paper microfluidic devices. The entire 3-D device is fabricated on a single sheet of flat paper in a single photolithographic step. It is assembled by simply folding the paper by hand. Following analysis, the device can be unfolded to reveal each layer. The applicability of the device to chemical analysis is demonstrated by colorimetric and fluorescence assays using multilayer microfluidic networks.

The chemical decompositions of beta-alaninediacetic acid (ADA) and diethylenetriaminepentaacetic acid (DTPA) were studied in a pilot-plant flow-through system simulating alkaline (pH 10-11) hydrogen peroxide bleaching environments. The amount of hydrogen peroxide decomposition was evaluated, and the distribution calculation was performed. Under the conditions investigated, ADA was more degradable than DTPA (average residual 71% vs 94%). The decomposition of hydrogen peroxide was not dependent on the chelate; the residual percent of hydrogen peroxide was 40 in both cases.

Pulping of blue agave waste, from the production of tequila, was evaluated by both chemical and biomechanical pulping processes. Two conventional and two organosolv systems were used to pulp the agave waste under a standard set of conditions. The soda-ethanol process was superior in terms of delignification and pulp properties in comparison to the soda and ethanol organosolv processes for pulping of agave waste; however, the kraft process gave the best strength properties. In general, the strength of the agave waste pulps was rather poor in comparison to wood and other agro-based pulps; however, the tear strength was relatively high. This result is typical of poorly bonded sheets and may be due to the coarseness of the agave fibers and/or loss of hemicelluloses in the steaming process for the tequila production. Fungal treatment of the agave waste with Ceriporiopsis subvermispora reduced the energy consumption for mechanical refining but gave biomechanical pulps with inferior strength properties. The blue agave chemical pulps should be suitable for blending with softwood kraft pulps for publication grade paper.

Surface treatment of biological tissue sections improves detection of peptides and proteins for mass spectrometry imaging. However, liquid surface treatments can result in diffusion of surface analytes and fragile tissue sections can be easily damaged by typical washing solvents. Here, we present a new surface washing procedure for mass spectrometry imaging. This procedure uses solvent wetted fiber-free paper to enable local washing of tissue sections for mass spectrometry imaging and tissue profiling experiments. In addition, the method allows fragile tissues that cannot be treated by conventional washing techniques to be analyzed by mass spectrometry imaging.

Bags impregnated with the organophosphorus pesticides prothiofos and cyanophos in three levels were used to cover Japanese apple-pears to protect them from insects. The amounts of prothiofos residue in the bags collected 4 months after application ranged from 0 to 34% of the amounts (81, 148, and 333 microg) found in the bags prior to a bagging. The amounts of cyanophos residue in bags collected 4 months after application ranged from 11 to 29% of the amounts (335, 2860, and 3740 microg) present prior to a bagging. Amounts of prothiofos found in fruits after 4 months ranged from 0 to 0.076 ppm. Amounts of cyanophos found in fruits after 4 months ranged from 0 to 0.011 ppm. Results of the present study indicate that these two pesticides migrated from pesticide-impregnated bags to fruits during the growing season.

A field-based metabolomic study was conducted during a shutdown of a pulp and paper mill (PPM) to assess the impacts of treated PPM effluent on endogenous polar metabolites in fathead minnow (FHM; Pimephales promelas) livers. Caged male and female FHMs were deployed at a Great Lakes area of concern during multiple periods (pre-, during, and post-shutdown) near the outflow for a wastewater treatment plant. Influent to this plant is typically 40% PPM effluent by volume. Additional FHMs were exposed to reference lake water under laboratory conditions. A bioassay using T47D-KBluc cells showed that estrogenic activity of receiving water near the outflow declined by 46% during the shutdown. We then used (1)H NMR spectroscopy and principal component analysis to profile abundances of hepatic endogenous metabolites for FHMs. Profiles for males deployed pre-shutdown in receiving water were significantly different from those for laboratory-control males. Profiles were not significantly different for males deployed during the shutdown, but they were significant again for those deployed post-shutdown. Impacts of treated effluent from this PPM were sex-specific, as differences among profiles of females were largely nonsignificant. Thus, we demonstrate the potential utility of field-based metabolomics for performing biologically based exposure monitoring and evaluating remediation efforts occurring throughout the Great Lakes and other ecosystems.

We previously produced a bactericidal filter paper loaded with PAA47-b-PS214 block copolymer micelles containing the biocide triclosan (TCN), using cationic polyacryamide (cPAM) as a binder. However, we encountered a very slow filtration, resulting in long bacteria deactivation times. Slow drainage occurred only when the filter paper was left to dry. It appears that the filter paper with cPAM and micelles develops hydrophobic properties responsible for this very slow filtration. Three approaches were taken to accelerate the very slow drainage all based on modification of binder-micelle interactions: (i) keeping the micelles wet, (ii) modification of the corona, and (iii) replacing cPAM with smaller and more highly charged cationic poly(isopropanol dimethylammonium) chloride (PIDMAC). In all cases, the drainage time of bactericidal filter paper became close to that of untreated filter paper, without decreasing its efficiency. Moreover, replacing cPAM with PIDMAC led to a much more efficient bactericidal filter paper that reduced bacteria viability by more than 6 orders of magnitude. In addition to resolving the hydrophobic drainage hurdle, the three solutions also offer a better understanding of the interaction between cPAM and micelles in the filter paper.

Surface sol-gel process was used to replicate the hierarchical morphology of natural cellulosic substances with nanometer precision. The resultant artificial fossils are ceramic nanomaterials composed of metal oxide nanotubes.

Room-temperature phosphorescence is observed from compounds placed onto a solid substrate, usually in the presence of a heavy-atom enhancer. In order to better understand the surface processes, x-ray photoelectron spectroscopy studies of the surface of Waltham No. 1 filter paper are performed before and after the spotting of a luminescent compound and/or heavy-atom solution onto the surface of the paper. Heavy atoms such as iodine and thallium, and the compounds 3,5-diiodotyrosine, 5-hydroxytryptophan, carbaryl, and bis(8-quinolinate)platinum(II) are used as probes. The observed chemical shifts and fractional areas of each class of carbon atom on the surface (as determined from computer curve fitting) are in reasonable accord with the molecular structure of the fiber. The different photoelectron peaks observed on the surface of the treated papers are identified and the elemental ratios determined. Variations in the binding energies and the elemental ratios provide information concerning changes in the surface composition.

Colored paper from magazines and newsprint was fed as 23% of a ration to sheep for 124 days. Among 44 elements determined in the paper and selected sheep tissues, marked accumulation of lead in animal organs was found reaching 22 ppm in bone. Barium and bromine was higher in kidney and fluorine was higher in bone of sheep fed the paper vs. the control ration. Histological examination of animal tissue revealed no apparent lesions which could be attributed to consumption of the paper diet. The sheep on the paper ration consumed more and gained weight at a faster rate than the control animals. The paper rations showed a higher in vivo digestibility than the control diet. 31 references.