Not exact matches
The reaction rate
between atmospheric hydrogen chloride (HCl) and chlorine nitrate (ClONO2) is greatly enhanced in the presence of ice
particles; HCl dissolves readily into ice, and the collisional reaction probability for ClONO2 on the surface of ice with HCl in the mole fraction range from ∼ 0.003 to 0.010 is in the range from ∼ 0.05 to 0.1 for temperatures near 200 K. Chlorine (Cl2) is released into the gas phase on a time scale of at most a few milliseconds, whereas nitric acid (HNO3), the other product, remains in the condensed phase.
And by carefully measuring and modeling the resulting changes in
atmospheric composition, scientists could improve their estimate of how sensitive Earth's climate is to CO2, said lead author Joyce Penner, a professor of
atmospheric science at the University of Michigan whose work focuses on improving global climate models and their ability to model the interplay
between clouds and aerosol
particles.
Using publically available data about wind speed and water vapor flux from real - world
atmospheric rivers over the Atlantic, the scientists created a computer model consisting of thousands of moving virtual air
particles and found a close match
between the complex swirls — the Lagrangian coherent structures — made by the air
particles and the patterns made by the real
atmospheric rivers.
They had assumed that
atmospheric water vapor had seeped into high - latitude martian soil and frozen
between soil
particles, forming a half - ice, half - soil mixture.
Contributions from the following topics (but not exclusively) are invited: • Solar irradiance and energetic
particle impacts on the atmosphere • Upper
atmospheric dynamical variability and coupling
between atmospheric layers • Solar variations and stratosphere - troposphere coupling • Solar influence on climate variability • Solar irradiance (spectral and total irradiance) variations
Understanding the climate impact of natural
atmospheric particles An international team of scientists, led by the University of Leeds, has quantified the relationship
between natural sources of
particles in the atmosphere and climate change.
Specifically, this chapter will examine the relationships
between the physical climate system and the land surface, the carbon cycle, chemically reactive
atmospheric gases and aerosol
particles.
Models that attempt to perform reliable projections of future climate changes should account explicitly for the feedbacks
between climate and the processes that determine the
atmospheric concentrations of greenhouse gases, reactive gases and aerosol
particles.
Mr. Nordhaus also omits any mention of the fact that the modelers had to insert fudge factors for
atmospheric particle concentrations to induce the models to predict the observed falling temperatures
between 1940 and 1960.