Exoplanet atmospheres

Abstract:

© 2018 Of the C3Hxhydrocarbons, propane (C3H8) and propyne (methylacetylene, CH3C2H) were first detected in Titan's atmosphere during the Voyager 1 flyby in 1980. Propene (propylene, C3H6) was first detected in 2013 with data from the Composite InfraRed Spectrometer (CIRS) instrument on Cassini. We present the first measured abundance profiles of propene on Titan from radiative transfer modeling, and compare our measurements to predictions derived from several photochemical models. Near the equator, propene is observed to have a peak abundance of 10 ppbv at a pressure of 0.2 mbar. Several photochemical models predict the amount at this pressure to be in the range 0.3–1 ppbv and also show a local minimum near 0.2 mbar which we do not see in our measurements. We also see that propene follows a different latitudinal trend than the other C3molecules. While propane and propyne concentrate near the winter pole, transported via a global convective cell, propene is most abundant above the equator. We retrieve vertical abundances profiles between 125 km and 375 km for these gases for latitude averages between 60°S–20°S, 20°S–20°N, and 20°N–60°N over two time periods, 2004 through 2009 representing Titan's atmosphere before the 2009 equinox, and 2012 through 2015 representing time after the equinox. Additionally, using newly corrected line data, we determined an updated upper limit for allene (propadiene, CH2CCH2, the isomer of propyne). We claim a 3-σ upper limit mixing ratio of 2.5 × 10−9 within 30° of the equator. The measurements we present will further constrain photochemical models by refining reaction rates and the transport of these gases throughout Titan's atmosphere.

Abstract:

Rocky planetesimals in the early solar system melted internally and evolved chemically due to radiogenic heating from 26Al. Here we quantify the parametric controls on magma genesis and transport using a coupled petrological and fluid mechanical model of reactive two-phase flow. We find the mean grain size of silicate minerals to be a key control on magma ascent. For grain sizes ≳1 mm, melt segregation produces distinct radial structure and chemical stratification. This stratification is most pronounced for bodies formed at around 1 Myr after formation of Ca, Al-rich inclusions. These findings suggest a link between the time and orbital location of planetesimal formation and their subsequent structural and chemical evolution. According to our models, the evolution of partially molten planetesimal interiors falls into two categories. In the magma ocean scenario, the whole interior of a planetesimal experiences nearly complete melting, which would result in turbulent convection and core–mantle differentiation by the rainfall mechanism. In the magma sill scenario, segregating melts gradually deplete the deep interior of the radiogenic heat source. In this case, magma may form melt-rich layers beneath a cool and stable lid, while core formation would proceed by percolation. Our findings suggest that grain sizes prevalent during the internal heating stage governed magma ascent in planetesimals. Regardless of whether evolution progresses toward a magma ocean or magma sill structure, our models predict that temperature inversions due to rapid 26Al redistribution are limited to bodies formed earlier than ≈1 Myr after CAIs. We find that if grain size was ≲1 mm during peak internal melting, only elevated solid–melt density contrasts (such as found for the reducing conditions in enstatite chondrite compositions) would allow substantial melt segregation to occur.