James D. Burke and Erik M. Conway
The Jet Propulsion Laboratory (JPL) of the California Institute of Technology had its origins in a student project to develop rocket propulsion in the late 1930s. It attracted funding from the U.S. Army just prior to U.S. entry into World War II and became an Army missile research facility in 1943. Because of its origins as a contractor-operated Army research facility, JPL is the National Aeronautics and Space Administration’s (NASA) only contractor-operated field center. It remains a unit of the California Institute of Technology. In the decades since its founding, the laboratory, first under U.S. Army direction and then as a NASA field center, has grown and evolved into an internationally recognized institution generally seen as a leader in solar system exploration but whose portfolio includes substantial Earth remote sensing.
JPL’s history includes episodes where the course of the laboratory’s development took turning points into new directions. After developing short-range ballistic missiles for the Army, the laboratory embarked on a new career in lunar and planetary exploration through the early 1970s and abandoned its original purpose as a propulsion technology laboratory. It developed the telecommunications infrastructure for planetary exploration too. It diversified into Earth science and astrophysics in the late 1970s and, due to a downturn in funding for planetary exploration, returned to significant amounts of defense work in the 1980s. The end of the Cold War between 1989 and 1991 resulted in a declining NASA budget, but support for planetary exploration actually improved within NASA management—as long as that exploration could be done more cheaply. This resulted in what is known as the “Faster Better Cheaper” period in NASA history. For JPL, this ended in 2000, succeeded by a return to more rigorous technical standards and increased costs.
Chemical and phase compositions of the surface of Venus could reflect a history of gas–rock and fluid–rock interactions, recent and past climate changes, and a loss of water from the Earth’s sister planet. The concept of chemical weathering on Venus through gas–solid type reactions was established in the early 1960s after the discovery of the hot and dense CO2-rich atmosphere of the planet, inferred from Earth-based and Mariner 2 radio emission data. Initial models suggested carbonation, hydration, and oxidation of exposed igneous rocks and a control (buffering) of atmospheric gases by solid–gas type chemical equilibria in the near-surface rocks. Carbonates, phyllosilicates and Fe oxides were considered likely secondary minerals. From the late 1970s onward, measurements of trace gases in the sub-cloud atmosphere by the Pioneer Venus and Venera entry probes and by Earth-based infrared spectroscopy challenged the likelihood of hydration and carbonation. The atmospheric H2O gas content appeared to be low enough to allow the stable existence of H2O-bearing and a majority of OH-bearing minerals. The concentration of SO2 gas was too high to allow the stability of Ca-rich carbonates and silicates with respect to sulfatization to CaSO4. In the 1980s, the detection of an elevated bulk S content at the Venera and Vega landing sites suggested ongoing consumption of atmospheric SO2 to surface sulfates. The supposed composition of the near-surface atmosphere implied oxidation of ferrous minerals to Fe oxides, magnetite and hematite, consistent with the infrared reflectance of surface materials. The likelihood of sulfatization and oxidation has been illustrated in modeling experiments in simulated Venus’ conditions. The morphology of Venus’ surface suggests contact of atmospheric gases with hot surface materials of mainly basaltic composition during the several hundreds of millions years since a global volcanic/tectonic resurfacing. Some exposed materials could have reacted at higher and lower temperatures in a presence of diverse gases at different altitudinal, volcanic, impact, and atmospheric settings. On highly deformed tessera terrains, more ancient rocks of unknown composition may reflect interactions with putative water-rich atmospheres and even aqueous solutions. Geological formations rich in salt, carbonate, Fe oxide, or silica will indicate past aqueous processes. The apparent diversity of affected solids, surface temperatures, pressures, and gas/fluid compositions throughout Venus’ history implies multiple signs of chemical alterations that remain to be investigated. The current understanding of chemical weathering is limited by the uncertain composition of the deep atmosphere, by the lack of direct data on the phase and chemical composition of surface materials, and by the uncertain data on thermodynamics of minerals and their solid solutions. In preparation for further atmospheric entry probe and lander missions, rock alteration could be investigated through chemical kinetic experiments and calculations of solid-gas/fluid equilibria to constrain past and present processes.
The planetary boundary layer of Mars is a crucial component of the Martian climate and meteorology, as well as a key driver of the surface-atmosphere exchanges on Mars. As such, it is explored by several landers and orbiters; high-resolution atmospheric modeling is used to interpret the measurements by those spacecrafts. The planetary boundary layer of Mars is particularly influenced by the strong radiative control of the Martian surface and, as a result, features a more extreme version of planetary boundary layer phenomena occurring on Earth. In daytime, the Martian planetary boundary layer is highly turbulent, mixing heat and momentum in the atmosphere up to about 10 kilometers from the surface. Daytime convective turbulence is organized as convective cells and vortices, the latter giving rise to numerous dust devils when dust is lifted and transported in the vortex. The nighttime planetary boundary layer is dominated by stable-layer turbulence, which is much less intense than in the daytime, and slope winds in regions characterized by uneven topography. Clouds and fogs are associated with the planetary boundary layer activity on Mars.