Distribution, ,movement,and evolution of the volatile elements in the lunar regolith

The abundances and distributions of carbon, nitrogen, and sulfur in lunar soils are reviewed. Carbon and nitrogen have a predominantly extra-lunar origin in lunar soils and breccias, while sulfur is mostly indigeneous to the Moon. The lunar processes which effect the movement, distribution, and evolution of carbon, nitrogen, and sulfur, along with the volatile alkali elements sodium, potassium, and rubidium during regolith processes are discussed. Possible mechanisms which may result in the addition to or loss from the Moon of these volatile elements are considered.     

The atmospheric entry of fine‐grained micrometeorites: The role of volatile gases in heating and fragmentation

The early stages of atmospheric entry are investigated in four large (250–950 μm) unmelted micrometeorites (three fine‐grained and one composite), derived from the Transantarctic Mountain micrometeorite collection. These particles have abundant, interconnected, secondary pore spaces which form branching channels and show evidence of enhanced heating along their channel walls. Additionally, a micrometeorite with a double‐walled igneous rim is described, suggesting that some particles undergo volume expansion during entry. This study provides new textural data which links together entry heating processes known to operate inside micrometeoroids, thereby generating a more comprehensive model of their petrographic evolution. Initially, flash heated micrometeorites develop a melt layer on their exterior; this igneous rim migrates inwards. Meanwhile, the particle core is heated by the decomposition of low‐temperature phases and by volatile gas release. Where the igneous rim acts as a seal, gas pressures rise, resulting in the formation of interconnected voids and higher particle porosities. Eventually, the igneous rim is breached and gas exchange with the atmosphere occurs. This mechanism replaces inefficient conductive rim‐to‐core thermal gradients with more efficient particle‐wide heating, driven by convective gas flow. Interconnected voids also increase the likelihood of particle fragmentation during entry and, may therefore explain the rarity of large fine‐grained micrometeorites among collections.     

Volatile transport on inhomogeneous surfaces: I – Analytic expressions,with application to Pluto’s day

The two orders of magnitude drop between the measured atmospheric abundances of non-radiogenic argon, krypton and xenon in Earth versus Mars is striking. Here, in order to account for this difference, we explore the hypothesis that clathrate deposits incorporated into the current martian cryosphere have sequestered significant amounts of these noble gases assuming they were initially present in the paleoatmosphere in quantities similar to those measured on Earth (in mass of noble gas per unit mass of the planet). To do so, we use a statistical-thermodynamic model that predicts the clathrate composition formed from a carbon dioxide-dominated paleoatmosphere whose surface pressure ranges up to 3 bars. The influence of the presence of atmospheric sulfur dioxide on clathrate composition is investigated and we find that it does not alter the trapping efficiencies of other minor species. Assuming nominal structural parameters for the clathrate cages, we find that a carbon dioxide equivalent pressure of 0.03 and 0.9 bar is sufficient to trap masses of xenon and krypton, respectively, equivalent to those found on Earth in the clathrate deposits of the cryosphere. In this case, the amount of trapped argon is not sufficient to explain the measured Earth/Mars argon abundance ratio in the considered pressure range. In contrast, with a 2% contraction of the clathrate cages, masses of xenon, krypton and argon at least equivalent to those found on Earth can be incorporated into clathrates if one assumes the trapping of carbon dioxide at equivalent atmospheric pressures of ～2.3 bar. The proposed clathrate trapping mechanism could have then played an important role in the shaping of the current martian atmosphere.     

Determining the local abundance of Martian methane and its’ 13C/12C and D/H isotopic ratios for comparison with related gas and soil analysis on the 2011 Mars Science Laboratory (MSL) mission

Understanding the origin of Martian methane will require numerous complementary measurements from both in situ and remote sensing investigations and laboratory work to correlate planetary surface geophysics with atmospheric dynamics and chemistry. Three instruments (Quadrupole Mass Spectrometer (QMS), Gas Chromatograph (GC) and Tunable Laser Spectrometer (TLS)) with sophisticated sample handling and processing capability make up the Sample Analysis at Mars (SAM) analytical chemistry suite on NASA’s 2011 Mars Science Laboratory (MSL) Mission. Leveraging off the SAM sample and gas processing capability that includes methane enrichment, TLS has unprecedented sensitivity for measuring absolute methane (parts-per-trillion), water, and carbon dioxide abundances in both the Martian atmosphere and evolved from heated soil samples. In concert with a wide variety of associated trace gases (e.g. SO₂, H₂S, NH₃, higher hydrocarbons, organics, etc.) and other isotope ratios measured by SAM, TLS will focus on determining the absolute abundances of methane, water and carbon dioxide, and their isotope ratios: ¹³C/¹²C and D/H in methane; ¹³C/¹²C and ¹⁸O/¹⁷O/¹⁶O in carbon dioxide; and ¹⁸O/¹⁷O/¹⁶O and D/H in water. Measurements near the MSL landing site will be correlated with satellite (Mars Express, Mars 2016) and ground-based observations.     

Mineralogy,chemistry, and irradiation record of Neuschwanstein (EL6) chondrite

Abstract– We present a detailed study of mineralogy, chemistry, and noble gases of the Neuschwanstein (EL6) chondrite that fell in 2002 in southern Germany. The meteorite has an unbrecciated texture and exhibits only minor shock features. Secondary weathering products are marginal. Neuschwanstein is an EL6 chondrite with heterogeneously distributed metal and sulfide grains. In terms of bulk chemistry, it has very high Fe concentrations, and siderophile and halogen element abundances higher than typical EL chondrites. However, like other ELs of higher petrologic type, it has low moderately volatile element abundances, e.g., Mn and Zn. We interpret these as indicators for loss of sulfide, probably through mobilization of ferroan alabandite and a Zn‐bearing sulfide, potentially sphalerite, during metamorphism. Trapped noble gases are dominated by a subsolar component with high Ar concentrations and are typical for EL chondrites. The shielding parameters indicate a small meteoroid (<20 cm radius) with an exposure age of approximately 47 Ma, which is among the highest for enstatite chondrites.     

Nitrogen and noble gases in micrometeorites

Abstract— Micrometeorites (MMs) currently represent the largest steady‐state mass flux of extraterrestrial matter to Earth and may have delivered a significant fraction of volatile elements and organics to the Earth's surface. Nitrogen and noble gases contents and isotopic ratios have been measured in a suite of 17 micrometeorites recovered in Antarctica (sampled in blue ice at Cap Prudhomme) and Greenland (separated from cryoconite) that have experienced variable thermal metamorphism during atmospheric entry. MMs were pyrolized using a CO₂ laser and the released gases were analyzed for nitrogen and noble gas abundances and isotopic ratios by static mass spectrometry after specific purification. Noble gases are a mixture of cosmogenic, solar, atmospheric, and possibly chondritic components, with atmospheric being predominant in severely heated MMs. δ¹⁵N values vary between ?240 ± 62‰ and +206 ± 12‰, with most values being within the range of terrestrial and chondritic signatures, given the uncertainties. Crystalline MMs present very high noble gas contents up to two orders of magnitude higher than carbonaceous chondrite concentrations. In contrast, nitrogen contents between 4 ppm and 165 ppm are much lower than those of carbonaceous chondrites, evidencing either initially low N content in MMs and/or degradation of phases hosting nitrogen during atmospheric entry heating and terrestrial weathering. Assuming that the original N content of MMs was comparable to that of carbonaceous chondrites, the contribution of nitrogen delivery by these objects to the terrestrial environment would have been probably marginal from 3.8 Gyr ago to present but could have been significant (?10%) in the Hadean, and even predominant during the latest stages of terrestrial accretion.     

Interrelationships among meteoric metals,meteors, interplanetary dust,micrometeorites, and meteorites

Abstract— Meteor science, aeronomy, and meteoritics are different disciplines with natural interfaces. This paper is an effort to integrate the chemistry and mineralogy of collected interplanetary dust particles (IDPs), micrometeorites, and meteorites with meteoric data and with atmospheric metal abundances. Evaporation, ablation, and melting of decelerating materials in the Earth's atmosphere are the sources of the observed metal abundances in the upper atmosphere. Many variables ultimately produce the materials and phenomena we can analyze, such as different accretion and parent‐body histories of incoming extraterrestrial materials, different interactions of meteors with the Earth's middle atmosphere, meteor data reduction, and complex chemical interactions of the metals and ions with the ambient atmosphere. The IDP‐like and unequilibrated ordinary chondrite matrix materials are reasonable sources for observed meteoric and atmospheric metals. The hypothesis of hierarchical dust accretion predicts that low, correlated refractory element abundances in cometary meteors may be real. It implies that the CI or cosmic standard is not useful to appreciate the chemistry of incoming petrologically heterogeneous cometary matter. The quasi steady‐state metal abundances in the lower thermosphere and upper mesosphere are derived predominantly from materials with cometary orbital characteristics and velocities such as comets proper and near‐Earth asteroids. The exact influence of atmospheric chemistry on these abundances still needs further evaluation. Metal abundances in the lower mesosphere and upper stratosphere region are mostly from materials from the asteroidal belt and the Kuiper belt.     

Heating experiments simulating atmospheric entry heating of micrometeorites: Clues to their parent body sources

Abstract— Depending on their velocity, entry angle and mass, extraterrestrial dust particles suffer certain degrees of heating during entry into Earth's atmosphere, and the mineralogy and chemical composition of these dust particles are significantly changed. In the present study, pulse-heating experiments simulating the atmospheric entry heating of micrometeoroids were carried out in order to understand the mineralogical and chemical changes quantitatively as well as to estimate the peak temperature experienced by the particles during entry heating. Fragments of the CI chondrites Orgueil and Alais as well as pyrrhotites from Orgueil were used as analogue material. The experiments show that the volatile elements S, Zn, Ga, Ge, and Se can be lost from 50 to 100 μm sized CI meteorite fragments at temperatures and heating times applicable to the entry heating of similar sized cosmic dust particles. It is concluded that depletions of these elements relative to CI as observed in micrometeorites are mainly caused by atmospheric entry heating. Besides explaining the element abundances in micrometeorites, the experimentally obtained release patterns can also be used as indicators to estimate the peak heating of dust particles during entry. Using the abundances of Zn and Ge and assuming their original concentrations close to CI, a maximum heating of 1100–1200 °C is obtained for previously analyzed Antarctic micrometeroites. Thermal alteration also strongly influenced the mineralogy of the meteorite fragments. While the unheated samples mainly consisted of phyllosilicates, these phases almost completely transformed into olivine and pyroxene in the fragments heated to ≥800 °C. Therefore, dust particles that still contain hydrous minerals were probably never heated to temperatures ≥800 °C in the atmosphere. During continued heating, the grain size of the newly formed silicates increased and the composition of the olivines equilibrated. Applying these results quantitatively to Antarctic micrometeorites, typical peak temperatures in the range of 1100–1200 °C during atmospheric entry heating are deduced. This temperature range corresponds to the one obtained from the volatile element concentrations measured in these micrometeorites and points to an asteroidal origin of the particles.     

Impacts as sources of the exosphere on Mercury

Chemical processes associated with meteoroid bombardment of Mercury are considered. Meteoroid impacts lead to production of metal atoms as well as metal oxides and hydroxides in the planetary exosphere. By using quenching theory, the abundances of the main Na-, K-, Ca-, Fe-, Al-, Mg-, Si-, and Ti-containing species delivered to the exosphere during meteoroid impacts were estimated. Based on a correlation between the solar photo rates and the molecular constants of atmospheric diatomic molecules, photolysis lifetimes of metal oxides and SiO are estimated. Meteoroid impacts lead to the formation of hot metal atoms (0.2-0.4 eV) produced directly during impacts and of very hot metal atoms (1-2 eV) produced by the subsequent photolysis of oxides and hydroxides in the exosphere of Mercury. The concentrations of impact-produced atoms of the main elements in the exosphere are estimated relative to the observed concentrations of Ca, assumed to be produced mostly by ion sputtering. Condensation of dust grains can significantly reduce the concentrations of impact-produced atoms in the exosphere. Na, K, and Fe atoms are delivered to the exosphere directly by impacts while Ca, Al, Mg, Si, and Ti atoms are produced by the photolysis of their oxides and hydroxides. The chemistry of volatile elements such as H, S, C, and N during meteoroid bombardment is also considered. Our conclusions about the temperature and the concentrations of impact-produced atoms in the exosphere of Mercury may be checked by the Messenger spacecraft in the near future and by BepiColombo spacecraft some years later.     

Carbon in Meteoroids: Wild 2 Dust Analyses, IDPs and Cometary Dust Analogues

Assuming that similar organic components as in comet 81P/Wild 2 are present in incoming meteoroids, we try to anticipate the observable signatures they would produce for meteor detection techniques. In this analysis we consider the elemental and organic components in cometary aggregate interplanetary dust particles and laboratory analyses of inter- and circumstellar carbon dust analogues. On the basis of our analysis we submit that (semi) quantitative measurements of H, N and C produced during meteor ablation will open an entire new aspect to using meteoroids as tracers of these volatile element abundances in active comets and their contributions to the mesospheric metal layers.     

Minimum estimates of the amount and timing of gases released into the martian atmosphere from volcanic eruptions

Volcanism has been a major process during most of the geologic history of Mars. Based on data collected from terrestrial basaltic eruptions, we assume that the volatile content of martian lavas was typically ∼0.5 wt.% water, ∼0.7 wt.% carbon dioxide, ∼0.14 wt.% sulfur dioxide, and contained several other important volatile constituents. From the geologic record of volcanism on Mars we find that during the late Noachian and through the Amazonian volcanic degassing contributed ∼0.8 bar to the martian atmosphere. Because most of the outgassing consisted of greenhouse gases (i.e., CO₂ and SO₂) warmer surface temperatures resulting from volcanic eruptions may have been possible. Our estimates suggest that ∼1.1 × 10²¹ g (∼8 ± 1 m m⁻²) of juvenile water were released by volcanism; slightly more than half the amount contained in the north polar cap and atmosphere. Estimates for released CO₂ (1.6 × 10²¹ g) suggests that a large reservoir of carbon dioxide is adsorbed in the martian regolith or alternatively ∼300 cm cm⁻² of carbonates may have formed, although these materials would not occur readily in the presence of excess SO₂. Up to ∼120 cm cm⁻² (2.2 × 10²⁰ g) of acid rain (H₂SO₄) may have precipitated onto the martian surface as the result of SO₂ degassing. The hydrogen flux resulting from volcanic outgassing may help explain the martian atmospheric D/H ratio. The amount of outgassed nitrogen (∼1.3 mbar) may also be capable of explaining the martian atmospheric ¹⁵N/¹⁴N ratio. Minor gas constituents (HF, HCl, and H₂S) could have formed hydroxyl salts on the surface resulting in the physical weathering of geologic materials. The amount of hydrogen fluoride emitted (1.82 × 10¹⁸ g) could be capable of dissolving a global layer of quartz sand ∼5 mm thick, possibly explaining why this mineral has not been positively identified in spectral observations. The estimates of volcanic outgassing presented here will be useful in understanding how the martian atmosphere evolved over time.     

Enceladus' plume: Compositional evidence for a hot interior

The combined observations of Saturn's moon Enceladus by the Cassini CAPS, INMS and UVIS instruments detected water vapor geysers in which were present molecular nitrogen (N₂), carbon dioxide (CO₂), methane (CH₄), propane (C₃H₈), acetylene (C₂H₂), and several other species, together with all of the decomposition products of water. We propose that the presence of N₂ in the plume indicates thermal decomposition of ammonia, and hence high temperatures in the interior of the moon (e.g., 500 to 800 K). Such an environment also appears to be suitable for the production of methane (CH₄) from carbon monoxide (CO), or carbon dioxide (CO₂). The presence of C₂H₂ and C₃H₈ strongly suggest that catalytic reactions took place within a very hot environment. The internal environment of Enceladus is inferred to be or have been favorable for aqueous, catalytic chemistry. This permits the synthesis of many complex organic compounds that could be detected in future Cassini observations.     

The origins of I‐type spherules and the atmospheric entry of iron micrometeoroids

The Earth's extraterrestrial dust flux includes a wide variety of dust particles that include FeNi metallic grains. During their atmospheric entry iron micrometeoroids melt and oxidize to form cosmic spherules termed I‐type spherules. These particles are chemically resistant and readily collected by magnetic separation and are thus the most likely micrometeorites to be recovered from modern and ancient sediments. Understanding their behavior during atmospheric entry is crucial in constraining their abundance relative to other particle types and the nature of the zodiacal dust population at 1 AU. This article presents numerical simulations of the atmospheric entry heating of iron meteoroids to investigate the abundance and nature of these materials. The results indicate that iron micrometeoroids experience peak temperatures 300–800 K higher than silicate particles explaining the rarity of unmelted iron particles which can only be present at sizes of <50 μm. The lower evaporation rates of liquid iron oxide leads to greater survival of iron particles compared with silicates, which enhances their abundance among micrometeorites by a factor of 2. The abundance of I‐types is shown to be broadly consistent with the abundance and size of metal in ordinary chondrites and the current day flux of ordinary chondrite‐derived MMs arriving at Earth. Furthermore, carbonaceous asteroids and cometary dust are suggested to make negligible contributions to the I‐type spherule flux. Events involving such objects, therefore, cannot be recognized from I‐type spherule abundances in the geological record.     

Sulfuric acid vapor and other cloud-related gases in the Venus atmosphere: Abundances inferred from observed radio opacity

Laboratory measurements of the microwave opacity of gaseous sulfuric acid under Venus atmospheric conditions indicate that it is an exceptionally strong absorber. They also suggest that its absorptivity has a surprisingly weak dependence on radio frequency, as compared with other common gaseous absorbers. Initial theoretical studies also indicate a large absorptivity and weak frequency dependence, although the measured opacity is several times the computed value, presumably due to deviations from Van Vleck-Weisskopf theory for pressures near and above about 1 atm. The absorbing characteristics of sulfuric acid vapor appear to reconcile what had been thought to be an inconsistency among measurements and deductions concerning the constituents of the atmosphere of Venus, and radio occultation, radar reflection, and radio emission measurements of its opacity. These and previous laboratory measurements of sulfur dioxide, water vapor, and carbon dioxide are used to model relative contributions to opacity as a function of height, in a way that is consistent with observations of the constituents and absorbing properties of the atmosphere. We conclude that sulfuric acid vapor is likely to be the principal microwave absorber in the 30- to 50-km-altitude range of the middle atmosphere of Venus. It would need to have a mixing ratio there of about 35 to 90 ppm if it were the sole absorber. Carbon dioxide, the predominant atmospheric gas, is the main absorber below about 30 km, while sulfur dioxide is an important but secondary absorber in both regions. Water vapor and cloud particulates appear to be only minor contributors to the total opacity. While gaseous sulfuric acid has not been directly measured in any of the in situ probe experiments (due to particular instrumental limitations), its presence at an abundance of the deduced order of magnitude is implied by these and other observations. We suggest that improved radio occultation measurements, in conjuction with high-resolution microwave emission observations and more detailed laboratory studies, could provide important data for investigating the sulfur compound chemistry in the atmosphere of Venus, and that the techniques and results may have application to the study of atmospheric conditions associated with acid rain on Earth.     

Sub-brown dwarfs as seats of life based on non-polar solvents: Thermodynamic restrictions

Sub-brown dwarfs (SBD) might originate either around a star or in solitary fashion. These bodies can retain atmospheres composed of molecular gases, which, upon cooling, have basal pressures of tens of bars or more. Pressure-induced opacity of these gases prevents such a body from eliminating its internal radioactive heat and its surface temperature can exceed the melting point of the life-supporting solvent for an extended period of time. Earth life uses water as a solvent but synthesis of observational data makes it possible to conceive chemical reactions that might support life involving non-carbon compounds, occurring in solvents other than water. In this paper a non-polar solvent is considered: ethane. Thermodynamic requirements to be fulfilled by a hypothetic gas constituent of a life-supporting SBD atmosphere are studied. Three gases are analyzed: nitrogen, carbon dioxide and methane. For thermodynamic reasons carbon dioxide is excluded from the list of candidate gases. We show that bodies with ethane oceans are possible in interstellar space. This may happen on SBD of (significantly) smaller or larger mass than the Earth. Generally, in case of SBD smaller in size than the Earth, the atmosphere exhibits a convective layer near the surface and a radiative layer at higher altitudes while the atmosphere of SBDs larger in size than Earth does not exhibit a convective layer. The prescribed thermodynamic state of ethane on the surface has some influence on the features of the atmosphere. The atmospheric mass of a life-hosting SBD of Earth size is two or three orders of magnitude larger than the mass of Earth atmosphere.     

Experimental laboratory simulation of Titan’s atmosphere: aerosols and gas phase

The discovery that Titan, the largest satellite of Saturn, has an atmosphere and that methane is a significant constituent of it, was the starting point for a systematic study of Titan’s atmospheric organic chemistry. Since then, the results from numerous ground-based observations and two flybys of Titan, by Voyager I and II, have led to experimental laboratory simulation studies and photochemical and physical modeling. All these works have provided a more detailed picture of Titan. We report here a continuation of such a study performing an experimental laboratory simulation of Titan’s atmospheric chemistry, and considering the two physical phases involved: gases and aerosols. Concerning the gaseous phase, we report the first detection of C₄N₂ and we propose possible atmospheric abundances for 70 organic compounds on Titan’s upper atmosphere. Concerning the solid phase, we have characterized aerosol analogues synthesized in conditions close to those of Titan’s environment, using elemental analysis, pyrolysis, solubility studies and infrared spectroscopy.     

Nitrogen Sulfide In Comets Hyakutake (C/1996 B2) And Hale–Bopp (C/1995 O1)

The chemistry of both nitrogen and sulfur presents interesting problems in comets.In this paper, we use a model of cometary comae with gas-phase chemical kineticsand gas dynamics to predict molecular abundances in the inner coma region for twoof the brightest comets in the past 20 years, Hyakutake (C/1996 B2) and Hale–Bopp(C/1995 O1). In this progress report we concentrate on the gas-phase chemistry of thenitrogen sulfide (NS) radical at a heliocentric distance of 1 AU to study the abundanceof NS using a detailed photo and chemical reaction network with over 100 species andabout 1000 reactions. The results are compared with recent observations of CometHale–Bopp and reveal that conventional gas-phase reactions schemes do not produceNS in sufficient quantities to explain the observations. We plan to continue therefinement of the model to improve agreement with observational constraints.     

A thermodynamic model of high temperature lava vaporization on Io

We modified the MAGMA chemical equilibrium code developed by Fegley and Cameron (1987, Earth Planet. Sci. Lett. 82, 207-222) and used it to model vaporization of high temperature silicate lavas on Io. The MAGMA code computes chemical equilibria in a melt, between melt and its equilibrium vapor, and in the gas phase. The good agreement of MAGMA code results with experimental data and with other computer codes is demonstrated. The temperature-dependent pressure and composition of vapor in equilibrium with lava is calculated from 1700 to 2400 K for 109 different silicate lavas in the ONaKFeSiMgCaAlTi system. Results for five lavas (tholeiitic basalt, alkali basalt, Barberton komatiite, dunite, and a molten type B1 Ca, Al-rich inclusion) are discussed in detail. The effects of continuous fractional vaporization on chemistry of these lavas and their equilibrium vapor are presented. The predicted abundances (relative to Na) of K, Fe, Si, Al, Ca, and Ti in the vapor equilibrated with lavas at 1900 K are lower than published upper limits for Io's atmosphere (which do not include Mg). We predict evaporative loss of alkalis, Fe, and Si during volcanic eruptions. Sodium is more volatile than K, and the Na/K ratio in the gas is decreased by fractional vaporization. This process can match Io's atmospheric Na/K ratio of 10±3 reported by Brown (2001, Icarus 151, 190-195). Silicon monoxide is an abundant species in the vapor above lavas. Spectroscopic searches are recommended for SiO at IR and mm wavelengths. Reactions of metallic vapors with S- and Cl-bearing volcanic gases may form other unusual gases including MgCl₂, MgS, MgCl, FeCl₂, FeS, FeCl, and SiS.     

Towards a quantitative understanding of atmospheric ozone

This review deals with the historical development of a chemical kinetics and photochemical data base for use in atmospheric modeling. Initiated by the suggestion that the release of nitric oxide into the stratosphere from the exhaust gases of supersonic aircraft could seriously deplete stratospheric ozone, the quest for such a data base began in 1971. The present article traces the development of the detailed chemistry of the homogeneous gas-phase reactions which control the levels of ozone in the stratosphere. It also includes coverage of the more recent heterogeneous chemistry which is believed to be involved in the Antarctic “ozone hole,” as well as the background to the on-going establishment of a reaction rate data base for application to tropospheric chemistry and modeling.     

Shock instabilities

It is well known that adiabatic shocks in ordinary gases are stable to both tranverse and longitudinal perturbations, but this need not be true if there are significant thermal effects due to chemical reactions or cooling processes. For example, detonation waves in gases are observed to form cellular structures if the chemical reaction is sufficiently temperature sensitive and a similar instability occurs in radiative shocks in the ISM if their speed exceeds 150 km s^–1. This means that interstellar shocks will be subject to this radiative instability in many cases. The temperature sensitivity of the nuclear reactions in Type I supernovae is also such that we would expect detonation waves in these objects to have a cellular structure.