University of New Hampshire

About: University of New Hampshire is a education organization based out in Durham, New Hampshire, United States. It is known for research contribution in the topics: Population & Solar wind. The organization has 9379 authors who have published 24025 publications receiving 1020112 citations. The organization is also known as: UNH.

Scaling laws of resistive magnetohydrodynamic reconnection in the high-Lundquist-number, plasmoid-unstable regime

Abstract: The Sweet–Parker layer in a system that exceeds a critical value of the Lundquist number (S) is unstable to the plasmoid instability. In this paper, a numerical scaling study has been done with an island coalescing system driven by a low level of random noise. In the early stage, a primary Sweet–Parker layer forms between the two coalescing islands. The primary Sweet–Parker layer breaks into multiple plasmoids and even thinner current sheets through multiple levels of cascading if the Lundquist number is greater than a critical value Sc≃4×104. As a result of the plasmoid instability, the system realizes a fast nonlinear reconnection rate that is nearly independent of S, and is only weakly dependent on the level of noise. The number of plasmoids in the linear regime is found to scales as S3/8, as predicted by an earlier asymptotic analysis [N. F. Loureiro et al., Phys. Plasmas 14, 100703 (2007)]. In the nonlinear regime, the number of plasmoids follows a steeper scaling, and is proportional to S. The thick...

Analysis of the atmospheric distribution, sources, and sinks of oxygenated volatile organic chemicals based on measurements over the Pacific during TRACE‐P

Abstract: Airborne measurements of a large number of oxygenated volatile organic chemicals (OVOC) were carried out in the Pacific troposphere (0.1-12 km) in winter/spring of 2001 (24 February to 10 April). Specifically, these measurements included acetone (CH3COCH3), methylethyl ketone (CH3COC2H5, MEK), methanol (CH3OH), ethanol (C2H5OH), acetaldehyde (CH3CHO), propionaldehyde (C2H5CHO), peroxyacylnitrates (PANs) (C(sub n)H(sub 2n+1)COO2NO2), and organic nitrates (C(sub n)H(sub 2n+1)ONO2). Complementary measurements of formaldehyde (HCHO), methyl hydroperoxide (CH3OOH), and selected tracers were also available. OVOC were abundant in the clean troposphere and were greatly enhanced in the outflow regions from Asia. Background mixing ratios were typically highest in the lower troposphere and declined toward the upper troposphere and the lowermost stratosphere. Their total abundance (Summation of OVOC) was nearly twice that of nonmethane hydrocarbons (Summation of C2-C8 NMHC). Throughout the troposphere, the OH reactivity of OVOC is comparable to that of methane and far exceeds that of NMHC. A comparison of these data with western Pacific observations collected some 7 years earlier (February-March 1994) did not reveal significant differences. Mixing ratios of OVOC were strongly correlated with each other as well as with tracers of fossil and biomass/biofuel combustion. Analysis of the relative enhancement of selected OVOC with respect to CH3Cl and CO in 12 plumes originating from fires and sampled in the free troposphere (3-11 km) is used to assess their primary and secondary emissions from biomass combustion. The composition of these plumes also indicates a large shift of reactive nitrogen into the PAN reservoir thereby limiting ozone formation. A three-dimensional global model that uses state of the art chemistry and source information is used to compare measured and simulated mixing ratios of selected OVOC. While there is reasonable agreement in many cases, measured aldehyde concentrations are significantly larger than predicted. At their observed levels, acetaldehyde mixing ratios are shown to be an important source of HCHO (and HO x ) and PAN in the troposphere. On the basis of presently known chemistry, measured mixing ratios of aldehydes and PANs are mutually incompatible. We provide rough estimates of the global sources of several OVOC and conclude that collectively these are extremely large (150-500 Tg C / yr) but remain poorly quantified.

CELIAS — Charge, Element and Isotope Analysis System for SOHO

Abstract: The CELIAS experiment on SOHO is designed to measure the mass, ionic charge and energy of the low and high speed solar wind, of suprathermal ions, and of low energy flare particles. Through analysis of the elemental and isotopic abundances, the ionic charge state, and the velocity distributions of ions originating in the solar atmosphere, the investigation focuses on the plasma processes on various temporal and spatial scales in the solar chromosphere, transition zone, and corona. CELIAS includes 3 mass- and charge-discriminating sensors based on the time-of-flight technique: CTOF for the elemental, charge and velocity distribution of the solar wind, MTOF for the elemental and isotopic composition of the solar wind, and STOF for the mass, charge and energy distribution of suprathermal ions. The instrument will provide detailed in situ diagnostics of the solar wind and of accelerated particles, which will complement the optical and spectroscopic investigations of the solar atmosphere on SOHO. CELIAS also contains a Solar Extreme Ultraviolet Monitor, SEM, which continously measures the EUV flux in a wide band of 17 – 70 nm, and a narrow band around the 30.4 nm He II line.