Observations of CO in the stratosphere of Venus via its J = 0 → 1 rotational transition

We have observed carbon monoxide in the stratosphere of Venus at phase angles of 180 and 120° via the J = 0 → 1 rotational transition at 115.2712 GHz. The mixing ratio profile of CO has been obtained by fitting the theoretical spectrum produced by a small number of layers with constant CO mixing ratio to the line profile, and the results suggest that the CO mixing ratio below the 1-mb level increased by at least a factor of 10 between 180 and 120° phase angles. The depletion of CO on the nightside of the planet was not anticipated and may require either a new loss mechanism for CO which can operate without sunlight or an increase in the amount of vertical mixing on the nightside.     

Thermal emission from a multiple scattering model of Saturn's rings

Models of Saturn's B ring have been investigated which include the shadowing mechanism, realistic phase functions for the ring particles, and the effects of multiple scattering and a particle size dispersion. These models are based on the assumption that the rings form a layer many particles thick. A power law relation dn ∝ ?^?s is used for the size dispersion law of the ring particles, where dn is the number of particles with radii between ? and ? + d?. In the calculation of the infrared brightness temperature of the rings, the effect of mutual heating among the ring particles is considered quantitatively for the first time. The parameters of the polydisperse s = 2 model can be chosen to satisfy both optical (λ ? 1.1 μ) and infrared data, but the situation could be much clarified if a good phase curve for the rings were available in the red, if the ring brightness were known accurately for λ > 1 μ, and if it could be established whether the ring particles are rotating synchronously.     

The HNC/HCN Ratio in Comets

The abundance ratio of the isomers HCN and HNC has been investigated in comet Hale-Bopp (C/1995 O1) through observations of the J = 4−3 rotational transitions of both species for heliocentric distances 0.93 < r < 3 AU, both pre- and post-perihelion. After correcting for the optical depth of the stronger HCN line, we find that the column density ratio of HNC/HCN in our telescope beam increases significantly as the comet approaches the Sun. We compare this behavior to that predicted from an ion-molecule chemical model and conclude that the HNC is produced insignificant measure by chemical processes in the coma; i.e., for comet Hale-Bopp, HNC is not a parent molecule sublimating from the nucleus. This revised version was published online in July 2006 with corrections to the Cover Date.     

The C3H2 2(20)-2(11) transition: absorption in cold dark clouds

The first observations of the 2(20)-2(11) transition of cyclopropenylidene (C3H2) at 21.6 GHz are described. In all cases where it has been detected, the line appears in absorption, showing that this transition is "refrigerated" (i.e., Tex < 2.7 K) in cold dust clouds. These results are compared with those for the 1(10)-1(01) transition of C3H2, and the consequences for the excitation of C3H2 qualitatively discussed.     

Interferometric observations for oxygen-containing organic molecules toward Orion-KL

High spatial resolution observations (approximately 5") were made for the 3 mm transitions of methanol (CH3OH), methyl formate (HCOOCH3), and dimethyl ether [(CH3)2O] toward Orion-KL using the Nobeyama Millimeter Array. The 15(3)-14(4) A- CH3OH emission appears to be elongated along the line connecting IRc2 and "the southern condensation (SC)", which may suggest a relation between methanol and the outflow from IRc2. The HCOOCH3 (7(1,6)-6(1,5)) and (CH3)2O (15(2,13)-15(1,14)) emissions appear to be well concentrated toward SC with an angular size of approximately 6".5 (at the 2 sigma level). There also exists another oxygen-rich condensation to the west of IRc2 (angular size approximately 4".5) having column densities of HCOOCH3 and (CH3)2O comparable to those of SC. We derive the total column densities 6.8 x 10(16) cm-2, 1.4 x 10(16) cm-2 and 2.7 x 10(16) cm-2 for CH3OH, HCOOCH3, and (CH3)2O, respectively, at the core of SC.     

Chemistry between the stars

Life--as we know it--is a chemical process, based on water and carbon compounds. Complex organic molecules are made primarily from the biogenic elements--carbon, hydrogen, nitrogen, oxygen, phosphorus and sulfur--that formed deep within massive ancient stars. How did these elements travel from their stellar birthplaces across time and space to make up the life-form that is reading these words? In this article, we'll take a look at the chemical processes that set the stage for the origin of life.     

Interstellar SiO as a tracer of high-temperature chemistry

The J = 2-1 transition of SiO has been searched for toward both hot and cold molecular gas. SiO was not detected toward the dark clouds TMC-1, L134 N, and B335, down to column density upper limits of N < 2-4 x 10(10) cm-2. The species, however, has been observed toward all sources with a kinetic temperature greater than or equal to 30 K, with the largest column densities (N approximately 10(13)-10(17) cm-2) measured in the warmest (TK > or = 100 K) material. The abundance of SiO, relative to HCN, is found to be approximately 0.1-1 in the massive star-forming regions toward Orion and NGC 7538; toward the dark clouds, the upper limits to this ratio is less than 0.0002-0.004. A similar enhancement in the warmer regions is reflected in the SiO/H2 ratio as well. A linear relation was found between the natural log of the SiO concentration and 1/TK, suggesting that the species' formation involves a chemically specific process that contains an activation barrier of approximately 90 K. SiO was also found to be underabundant with respect to SO in cold clouds, with SiO/SO < 1/1000, versus SiO/SO > or =, measured in Orion-KL. The formation of SiO is therefore linked closely to the local gas kinetic temperature, rather than the oxygen abundance, and its synthesis is likely to involve high-temperature gas-phase reactions. The species thus may serve as an unambiguous indicator of high-temperature or "shock" chemistry.     

Tricarbon monoxide in TMC-1

We report the measurement of three new lines of C3O in TMC-1. The observed peak antenna temperatures, appropriately corrected for atmospheric and telescope losses, are found to be consistent with a large velocity gradient radiative transfer model whose parameters span the range of standard values for this cloud. The derived fractional abundance for C3O is 1.4 x 10(-10), comparable with the results predicted from a model calculation based on a gas-phase ion-molecule reaction scheme. The results of negative searches for C3O in six other sources are not inconsistent with expected conditions in these clouds.     

The detection of acetaldehyde in cold dust clouds

Observations of the 1(01) --> 0(00) rotational transitions of A and E state acetaldehyde are reported. The transitions were detected, for the first time in interstellar space, in the cold dust clouds TMC-1 and L134N, and in Sgr B2. This is also the first time acetaldehyde has been found in a dust cloud and is the most complex oxygen-bearing molecule yet known in this environment. We find a column density of 6 x 10(12) cm-2 in TMC-1, comparable to many other species detected there, and an approximately equal column density in L134N. In the direction of Sgr B2, the CH3CHO profile appears to consist of broad emission features from the hot molecular cloud core, together with absorption features resulting from intervening colder material. We also report the possible detection of HC9N toward IRC +10 degrees 216 through its J = 33 --> 32 transition. Implications for cold dust cloud chemistry and excitation are discussed.     

A study of C3HD in cold interstellar clouds

We have detected the 1(10)-1(01) transition of C3HD at 19.418 GHz at twelve positions in cold, dark clouds and resolved the D hyperfine components in two sources (L1498 and TMC-1C) well enough to derive values for the D quadrupole coupling constants. Simultaneous observations of C3H2 in each source yield relative integrated line intensities in the range 0.10-0.18, from which we derive relative [C3HD]/[C3H2] abundances in the range 0.05-0.15. These are among the highest deuteration ratios yet observed. Within the limits of the observational and modeling uncertainties it is possible to explain the derived [C3HD]/[C3H2] ratios by ion-molecule chemistry if [e-] approximately 3 x 10(-7).