5,936 research outputs found
Mercury deposition in southern New Hampshire, 2006–2009
The atmospheric deposition of mercury (Hg) occurs via several mechanisms including wet, dry, and occult processes. In an effort to understand the atmospheric cycling and seasonal depositional characteristics of Hg, event-based wet deposition samples and reactive gaseous Hg (RGM) measurements were collected for approximately 3 years at Thompson Farm (TF), a near-coastal rural site in Durham, NH, part of the University of New Hampshire AIRMAP Observing Network. Total aqueous mercury exhibited seasonal patterns in Hg wet deposition at TF. The lowest Hg wet deposition was measured in the winter with an average total seasonal deposition of 1.56 μg m−2compared to the summer average of 4.71 μg m−2. Inter-annual differences in total wet deposition are generally linked with precipitation volume, with the greatest deposition occurring in the wettest year. Relationships between surface level RGM and Hg wet deposition were also investigated based on continuous RGM measurements at TF from November 2006 to September 2009. No correlations were observed between RGM mixing ratios and Hg wet deposition, however the ineffective scavenging of RGM during winter precipitation events was evidenced by the less frequent depletion of RGM below the detection level. Seasonal dry deposition of reactive gaseous Hg (RGM) was estimated using an order-of-magnitude approach. RGM mixing ratios and dry deposition estimates were greatest during the winter and spring. The seasonal ratios of Hg wet deposition to RGM dry deposition vary by up to a factor of 80
Maximal quantum yield of photosynthesis in the northwestern Sargasso Sea
The magnitude and variability of the maximal quantum yield of photosynthesis were examined in the northwestern Sargasso Sea in April 1985. Maximal quantum yield was calculated from light-limited photosynthetic rates and spectrally-weighted absorption coefficients. The absorption by total particulates collected on a glass fiber filter was partitioned into two components, one associated with living phytoplankton and one associated with other absorbing particles. Two types of maximal quantum yield were calculated: one from the absorption by total particulates and one from the absorption by the phytoplanktonic component alone. Maximal quantum yield calculated from absorption by total particulates was low [0.014 to 0.071 mol C (mol photons)–1] and decreased as the proportion of absorption due to the non phytoplanktonic particles increased. The phytoplanktonic maximal quantum yield was higher [0.033 to 0.102 mol C (mol photons)–1] and varied by a factor of two over a period of two weeks during and following a spring bloom. Use of the phytoplanktonic component of absorption to calculate maximal quantum yield allowed analysis of changes in maximal quantum yield as a function of changes in phytoplankton physiology rather than changes in the amount of absorption by particulate detritus. The pattern of variation in quantum yield was related to nitrogen flux; these data suggest that maximal quantum yield can be predicted from environmental conditions on a regional or seasonal basis
Nitric acid scavenging by mineral and biomass burning aerosols
The abundance of gas phase nitric acid in the upper troposphere is overestimated by global chemistry-transport models, especially during the spring and summer seasons. Recent aircraft data obtained over the central US show that mineral aerosols were abundant in the upper troposphere during spring. Chemical reactions on mineral dust may provide an important sink for nitric acid. In regions where the mineral dust abundance is low in the upper troposphere similar HNO3 removal processes may occur on biomass burning aerosols. We propose that mineral and biomass burning aerosols may provide an important global sink for gas phase nitric acid, particularly during spring and summer when aerosol composition in the upper troposphere may be greatly affected by dust storms from east Asia or tropical biomass burning plumes
Analysis of Granular Flow in a Pebble-Bed Nuclear Reactor
Pebble-bed nuclear reactor technology, which is currently being revived
around the world, raises fundamental questions about dense granular flow in
silos. A typical reactor core is composed of graphite fuel pebbles, which drain
very slowly in a continuous refueling process. Pebble flow is poorly understood
and not easily accessible to experiments, and yet it has a major impact on
reactor physics. To address this problem, we perform full-scale,
discrete-element simulations in realistic geometries, with up to 440,000
frictional, viscoelastic 6cm-diameter spheres draining in a cylindrical vessel
of diameter 3.5m and height 10m with bottom funnels angled at 30 degrees or 60
degrees. We also simulate a bidisperse core with a dynamic central column of
smaller graphite moderator pebbles and show that little mixing occurs down to a
1:2 diameter ratio. We analyze the mean velocity, diffusion and mixing, local
ordering and porosity (from Voronoi volumes), the residence-time distribution,
and the effects of wall friction and discuss implications for reactor design
and the basic physics of granular flow.Comment: 18 pages, 21 figure
Evaluation of Dynamic Cell Processes and Behavior Using Video Bioinformatics Tools
Just as body language can reveal a person’s state of well-being, dynamic changes in cell behavior and
morphology can be used to monitor processes in cultured cells. This chapter discusses how CL-Quant
software, a commercially available video bioinformatics tool, can be used to extract quantitative data on:
(1) growth/proliferation, (2) cell and colony migration, (3) reactive oxygen species (ROS) production, and
(4) neural differentiation. Protocols created using CL-Quant were used to analyze both single cells and
colonies. Time-lapse experiments in which different cell types were subjected to various chemical
exposures were done using Nikon BioStations. Proliferation rate was measured in human embryonic stem
cell colonies by quantifying colony area (pixels) and in single cells by measuring confluency (pixels).
Colony and single cell migration were studied by measuring total displacement (distance between the
starting and ending points) and total distance traveled by the colonies/cells. To quantify ROS production,
cells were pre-loaded with MitoSOX Red™, a mitochondrial ROS (superoxide) indicator, treated with
various chemicals, then total intensity of the red fluorescence was measured in each frame. Lastly, neural
stem cells were incubated in differentiation medium for 12 days, and time lapse images were collected
daily. Differentiation of neural stem cells was quantified using a protocol that detects young neurons. CLQuant
software can be used to evaluate biological processes in living cells, and the protocols developed in
this project can be applied to basic research and toxicological studies, or to monitor quality control in
culture facilities
Dynamic landscapes in northwestern North America structured populations of wolverines (Gulo gulo)
Response properties in a model for granular matter
We investigate the response properties of granular media in the framework of
the so-called {\em Random Tetris Model}. We monitor, for different driving
procedures, several quantities: the evolution of the density and of the density
profiles, the ageing properties through the two-times correlation functions and
the two-times mean-square distance between the potential energies, the response
function defined in terms of the difference in the potential energies of two
replica driven in two slightly different ways. We focus in particular on the
role played by the spatial inhomogeneities (structures) spontaneously emerging
during the compaction process, the history of the sample and the driving
procedure. It turns out that none of these ingredients can be neglected for the
correct interpretation of the experimental or numerical data. We discuss the
problem of the optimization of the compaction process and we comment on the
validity of our results for the description of granular materials in a
thermodynamic framework.Comment: 22 pages, 35 eps files (21 figures
Photochemistry in the arctic free troposphere: NOx budget and the role of odd nitrogen reservoir recycling
The budget of nitrogen oxides (NOx) in the arctic free troposphere is calculated with a constrained photochemical box model using aircraft observations from the Tropospheric O3 Production about the Spring Equinox (TOPSE) campaign between February and May. Peroxyacetic nitric anhydride (PAN) was observed to be the dominant odd nitrogen species (NOy) in the arctic free troposphere and showed a pronounced seasonal increase in mixing ratio. When constrained to observed acetaldehyde (CH3CHO) mixing ratios, the box model calculates unrealistically large net NOx losses due to PAN formation (62pptv/day for May, 1-3km). Thus, given our current understanding of atmospheric chemistry, these results cast doubt on the robustness of the CH3CHO observations during TOPSE. When CH3CHO was calculated to steady state in the box model, the net NOx loss to PAN was of comparable magnitude to the net NOx loss to HNO3 (NO2 reaction with OH) for spring conditions. During the winter, net NOx loss due to N2O5 hydrolysis dominates other NOx loss processes and is near saturation with respect to further increases in aerosol surface area concentration. NOx loss due to N2O5 hydrolysis is sensitive to latitude and month due to changes in diurnal photolysis (sharp day-night transitions in winter to continuous sun in spring for the arctic). Near NOx sources, HNO4 is a net sink for NOx; however, for more aged air masses HNO4 is a net source for NOx, largely countering the NOx loss to PAN, N2O5 and HNO3. Overall, HNO4 chemistry impacts the timing of NOx decay and O3 production; however, the cumulative impact on O3 and NOx mixing ratios after a 20-day trajectory is minimal. © 2003 Elsevier Science Ltd. All rights reserved
Recommended from our members
Characterization of the chemical signatures of air masses observed during the PEM experiments over the western Pacific
Extensive observations of tropospheric trace species during the second NASA Global Tropospheric Experiment Western Pacific Exploratory Mission (PEM-West B) in February-March 1994 showed significant seasonal variability in comparison with the first mission (PEM-West A), conducted in September-October 1991. In this study we adopt a previously established analytical method, i.e., the ratio C2H2/CO as a measure of the relative degree of atmospheric processing, to elucidate the key similarities and variations between the two missions. In addition, the C2H2/CO ratio scheme is combined with the back-trajectory-based and the LIDAR-based air mass classification schemes, respectively, to make in-depth analysis of the seasonal variation between PEM-West A and PEM-West B (hereinafter referred to as PEM-WA and PEM-WB). A large number of compounds, including long-lived NMHCs, CH4, and CO2, are, as expected, well correlated with the ratio C2H2/CO. In comparison with PEM-WA, a significantly larger range of observed C2H2/CO values at the high end for the PEM-WB period indicates that the western Pacific was more impacted by "fresher" source emissions, i.e., faster or more efficient continental outflow. As in the case of PEM-WA, the C2H2/CO scheme complements the back-trajectory air mass classification scheme very well. By combining the two schemes, we found that the atmospheric processing in the region is dominated by atmospheric mixing for the trace species analyzed. This PEM-WB wintertime result is similar to that found in PEM-WA for the autumn. In both cases, photochemical reactions are found to play a significant role in determining the background mixing ratios of trace gases, and in this way the two processes are directly related and dependent upon each other. This analysis also indicates that many of the upper tropospheric air masses encountered over the western Pacific during PEM-WB may have had little impact from eastern Asia's continental surface sources. NOx mixing ratios were significantly enhanced during PEM-WB when compared with PEM-WA, in the upper troposphere's more atmospherically processed air masses. These high levels of NOx resulted in a substantial amount of photochemical production of O3. A lack of corresponding enhancements in surface emission tracers strongly implies that in situ atmospheric sources such as lightning are responsible for the enhanced upper tropospheric NOx. The similarity in NOx values between the northern (higher air traffic) and southern continental air masses together with the indications of a large seasonal shift suggests that aircraft emissions are not the dominant source. However, photochemical recycling cannot be ruled out as this in situ source of NOx. Copyright 1999 by the American Geophysical Union
Cutting Ties with Pro-Ana: A Narrative Inquiry Concerning the Experiences of Pro-Ana Disengagement from Six Former Site Users.
Websites advocating the benefits of eating disorders (“Pro-Ana”) tend to reinforce and maintain restrictive eating and purging behaviors. Yet remarkably, no study has explored individual accounts of disengagement from these sites and the associated meanings. Using narrative inquiry, this study sought to address this gap. From the interviews of six women, two overarching storylines emerged. The first closely tied disengagement to recovery with varying positions of personal agency claimed: this ranged from enforced and unwelcomed breaks that ignited change, to a personal choice that became viable through the development of alternative social and personal identities. A strong counternarrative to “disengagement as recovery” also emerged. Here, disengagement from Pro-Ana was storied alongside a need to retain an ED lifestyle. With “recovery” being just one reason for withdrawal from Pro-Ana sites, clinicians must remain curious about the meanings individuals ascribe to this act, without assuming it represents a step toward recovery.Peer reviewedFinal Accepted Versio
- …