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At least 271 records · Page 15

X-Ray and Infrared Observations of Embedded Young Stars in NGC 2264

Images of the NGC 2264 star-forming region, which we have acquired with the XMM-Newton spacecraft, reveal strong X-ray emission from three deeply embedded (Av > 10 mag) young stellar objects in the vicinity of Allen's infrared source (AFGL 989 = IRS 1) and Castelaz & Grasdalen s infrared source (RNO-EW = IRS 2). Thermal plasma models for the brightest source in X-rays, located 11 southwest of Allen's star, yield a quasi-steady luminosity of Lx = 10 ergs s-1 and an extraordinarily high X-ray temperature of 100 MK. The high temperature is consistent with the presence of emission lines of Fe xxv and Fe xxvi at photon energies of 6.7 and 6.9 keV, respectively. An even higher temperature of nearly 140 MK was observed during the rise phase of a powerful impulsive X-ray flare of another young star in the IRS 2 region. Moderate-resolution near-infrared (1-4 um) spectra of the embedded objects, obtained at the NASA Infrared Telescope Facility, exhibit deep water ice absorption bands, as well as a variety of emission and absorption features of H I, CO, and both neutral and ionized metals.

Simon, Theordore↗

Lunar Impact Melt Crystallization Produces Reflectance Spectra Dominated By Clinopyroxene Signatures: Implications for the Origin of Pink Spinel Anorthosite

Magma-wallrock interaction and impact melt crystallization are the two leading hypotheses for the formation of orbitally detected lunar “pink” spinel anorthosite (PSA) [1-3]. Distinguishing among hypotheses is complicated because both require mixing of anorthositic crust and MgO-rich ultramafic components. Models for PSA formation need to account for either the thermodynamic hurdles of crustal assimilation, or the size of impactor and composition of target material needed to generate spinel during crater and basin formation. Determining whether the energy source is endogenic or exogenic is important for understanding the thermal and chemical evolution of the lunar crust. Here we test the impact melt hypothesis by performing controlled cooling experiments on two hypothetical impact melt compositions. The compositions represent mixing of ultramafic magma and anorthositic crust in molar ratios of approximately 50:50 and 25:75. Synthetic crystallized assemblages were prepared for chemical analysis and bidirectional reflectance spectroscopy in the visible to near-infrared wavelengths. All crystallization experiments contained plagioclase, olivine, and clinopyroxene, but trace amounts of spinel were only observed in the 50:50 mix. The experimental spinel is similar to the compositions inferred from remote observations. However, the high-Ca pyroxene in our experimental assemblages (9 – 18 wt.%) resulted in 1 and 2 µm absorption band center positions consistent with synthetic clinopyroxene. The clinopyroxene absorptions are present regardless of specific mineral modes and the presence of either olivine or spinel. These results suggest that impact melt crystallization will produce clinopyroxene-bearing lithologies, the presence of which masks spectral contributions from coexisting spinel and olivine. Assuming that the trace amounts of spinel observed in our experiments could be concentrated and isolated from the mafic silicates by convection or density settling in the impact melt sheet, the spinel-rich areas would still be proximally associated with the remaining silicate-dominated assemblage exhibiting strong clinopyroxene spectral signatures. We conclude that impact melting of the lunar crust can explain rare cases of PSA in association with clinopyroxene. Previous investigations of magma-wallrock interactions [2] demonstrate that small plagioclase-contaminated regions of an ultramafic intrusion can concentrate spinel whereas larger portions of the same intrusion remain relatively uncontaminated and yield olivine and orthopyroxene, consistent with the more common occurrence of PSAs in association with orthopyroxene ±olivine in the remote sensing database (e.g., Moscoviense Basin) [4].

petrology↗

Atmospheric Oxygen Photoabsorption

The work conducted on this grant was devoted to various aspects of the photophysics and photochemistry of the oxygen molecule. Predissociation linewidths were measured for several vibrational levels in the O2(B3 Sigma(sub u)(sup -)) state, providing good agreement with other groups working on this important problem. Extensive measurements were made on the loss kinetics of vibrationally excited oxygen, where levels between v = 5 and v = 22 were investigated. Cavity ring-down spectroscopy was used to measure oscillator strengths in the oxygen Herzberg bands. The great sensitivity of this technique made it possible to extend the known absorption bands to the dissociation limit as well as providing many new absorption lines that seem to be associated with new O2 transitions. The literature concerning the Herzberg band strengths was evaluated in light of our new measurements, and we made recommendations for the appropriate Herzberg continuum cross sections to be used in stratospheric chemistry. The transition probabilities for all three Herzberg band systems were re-evaluated, and we are recommending a new set of values.

Slanger, Tom G.↗

Optical properties of CO2 ice and CO2 snow in the ultraviolet, visible, and infrared

The project was to measure the optical constants of CO2 ice in the spectral regions of weak absorption. Many previous measurements had been made by others in the strong absorption bands, but the weak regions had been poorly measured or not measured at all. In these regions the emissivity of CO2 frost and CO2 clouds is quite sensitive to particle sizes and to the value of the absorption coefficient, so the new measurements will have applications to energy budget and remote sensing of the Martian surface and atmosphere. During the time period covered by this grant, a method was developed for growing clear crystals of CO2, 4 cm in length. An apparatus was constructed for accurate measurement of spectral transmission through these crystals, for wavelengths 0.18-3.8 micrometers, covering the near-ultraviolet, visible, and near-infrared regions, bounded by the strong ultraviolet absorption and the 4.3-micrometer band. Our new best estimate of the spectral absorption coefficient (expressed as imaginary refractive index) is shown. It is a composite result of many measurements on dozens of crystals. Now that we have a good dataset for the shortwave absorption spectrum, the focus of the research has moved to the thermal infrared, for which a Fourier Transform interferometer has been adapted for use with C02-ice crystals.

Warren, Stephen↗

An interstellar cloud density from Copernicus observations of CO in the spectrum of Zeta Ophiuchi

Interstellar CO absorption bands in Copernicus spectra of Zeta Oph have been studied. Absorption profiles, computed under the assumption that excitation is due to collisions with H2 molecules and interaction with the 3-K background radiation field, were fitted to the reduced data of nine bands. When a gas kinetic temperature of 56 K is assumed, the best-fit condition implies a hydrogen-nucleus density of 120 per cu cm, a CO column density of 1.2 by 10 to the 15th power per sq cm, and a radial-velocity dispersion of 0.9 km/s. The relevance of these results to existing ideas concerning the Zeta Oph interstellar clouds is discussed. It is suggested that the strongest interstellar component is not circumstellar in origin but is instead part of a supernova remnant. Simple calculations are made to establish the plausibility of the supernova-remnant identification. This suggestion is also supported by Heiles's (1976) 21-cm pictures.

Smith, A. M.↗

Organic Molecules On the Surfaces of Iapetus and Phoebe

Absorption bands of both aliphatic and aromatic organic molecules are found in the reflectance spectra of Saturn satellites Iapetus, Phoebe, and Hyperion obtained with the Cassini Visible-Infrared Mapping Spectrometer (VIMS). The VIMS data do not fully resolve the individual bands of C-H functional groups specific to particular molecules, but instead show absorption envelopes representing blended clusters of the bands of aromatic (approximately 3.28 microns) and aliphatic (approximately 3.4 microns) hydrocarbons known in spectra of interstellar dust. In Cruikshank et al. (2014), we matched components of the unresolved hydrocarbon band envelopes with clusters of bands of a range of functional groups in specific types of organic compounds (e.g., normal and N-substituted polycyclic aromatic hydrocarbons, olefins, cycloalkanes, and molecules with lone-pair interactions of N and O with CH3+). In the work reported here, we revisit the spectra of Iapetus and Phoebe using VIMS data processed with improved radiometric and wavelength calibration (denoted RC19). The band envelopes of both aromatic and aliphatic hydrocarbons are now more clearly defined, corroborating the provisional assignment of specific classes of molecules in Cruikshank et al. 2014, but permitting a more reliable quantitative assessment of the relative contributions of those classes, and a revision to the earlier estimate of the ratio of the abundances of aromatic to aliphatic molecules.

Phoeb↗

Spot temperatures and area coverages on active dwarf stars

Two active K dwarfs are examined to determine the temperatures of the stars and to estimate the locations and sizes of cool spots on the stellar surfaces. Two wavelength regions with TiO absorption bands at different temperature sensitivities are modeled simultaneously using the method developed by Huenemoerder and Ramsey (1987). The spectrum of BD +26deg730 shows excess absorption in the TiO band, and the absence of the 8860 A band in HD 82558 indicates that its spots are warmer than those of BD +26deg730.

Sarr, Steven H.↗

Spatially resolved reflectivities of Jupiter during the 1976 opposition

Spatially resolved absolute reflectivities of several regions of the Jovian disk in the wavelength region 3000 to 10760 A are presented. Spectra were obtained of the central meridian and limbs of the Equatorial Region, North Equatorial Belt, and North Tropical Zone. Equivalent widths of several CH4 and NH3 bands are measured. The spatial variations of continuum reflectivity and absorption band profiles are shown in various ratio spectra.

Woodman, J. H.↗

Reflectance spectroscopy - Quantitative analysis techniques for remote sensing applications

The empirical methods and scattering theories that are important for solving remote sensing problems are among the methods for remotely sensed reflectance data analysis presently compared. In the case of the photon mean optical path length concept's implications for reflectance spectra modeling, it is shown that the mean optical path length in a particulate surface is in roughly inverse proportion to the square root of the absorption coefficient. Absorption bands, which are Gaussian in shape when plotted as true absorptance vs photon energy, are also Gaussians in apparent absorptance, although they have a smaller intensity. An apparent continuum in a reflectance spectrum is modeled as a mathematical function that is used to isolate a particular absorption feature for analysis, and it is noted that this continuum should be removed by dividing it into the reflectance spectrum.

Clark, R. N.↗

Basalts of Mars: Constraints on Volatile Evolution

The mineralogy of relatively unweathered rocks on Mars place important constraints on models of planetary oxidation state, volcanism and associated outgassing, accretion and associated volatile inventory, and geochemical changes over time. Reflectance spectra (300 to 2500 nm) provide direct mineralogic information about the surface materials. Spectra measured using Earth-based telescopes were analyzed by a multiple high-order derivative spectroscopy technique. Nine areas, measured during the 1978 opposition, were analyzed by the technique. Each contained suites of well-defined absorption bands. These bands can be interpreted in terms of constituent mineralogy by the technique of Adams. Among the features extracted from the spectra were bands attributed to iron oxides. Other bands can be attributed to silicates within chemically unweathered rocks/fines. Absorption features suggest the presence of Mg-olivine and plagioclase feldspar.

Huguenin, R. L.↗

Inter-comparison of Wildfire and High-resolution Interferometer Sounder (HIS) data from STORM-FEST: An investigation of wildfire spectral channel discrepancies

This simultaneous collection of HIS spectral measurements aboard the ER-2 during STORM-FEST provided a means to explore calibration problems in the infrared bands of the Wildfire instrument. Large discrepancies in brightness temperatures were noted in Wildfire bands designed to sample the 'wings' of the strong ozone absorption band centered at 9.6 microns, where the atmospheric transmittance changes rapidly with wavelength. Examination of interchannel relationships in Wildfire data and subsequent comparison to Wildfire data synthesized from the HIS measurements suggests that a wavelength shift in the channel spectral response from those determined in the laboratory may have occurred. Based on comparisons from several flights, this spectral shift has been empirically determined to be about 0.15 micron. It is speculated that this problem resulted from a slight misalignment of the spectrometer grating or other optical elements, or was a result of extreme range in temperatures experienced by the instrument throughout the course of an ER-2 flight. A consequence of this temperature fluctuation may be a change in a position of the grating in the optical path and could result in the variations in channel spectral response during flight. These findings for Wildfire may have significant bearing on future use of the MAS because of the similarities to the original Wildfire configuration.

Jedlovec, G. J.↗

The detection of a new strong band near 3590 cm(exp -1) (2.79 microns) in the spectrum of Io

A strong absorption band at 3590 +/- 20 cm(exp -1) (2.790 +/- 0.015 microns) has been discovered in the spectrum of Io using the Kuiper Airborne Observatory (KAO). The 2 nu(sub 1) + nu(sub 3) combination mode of solid SO2 falls at this position. Since SO2 is abundant on Io it must contribute to the new band. However, a band due to H2O was also predicted near this frequency in Io's spectrum based on laboratory experiments of H2O:SO2 mixed Io ice analogs which were used to assign the two weak, variable features at 3370 and 3170 cm(exp -1) (2.97 and 3.15 microns) to trace amounts of H2O frozen in solid SO2 on Io. The new band probably originates from both SO2 and H2O. Unfortunately, the spectral resolution of the data is insufficient to settle the issue of whether or not there are two resolvable components.

Salama, F.↗

Theoretical calculations on the electron absorption spectra of selected Polycyclic Aromatic Hydrocarbons (PAH) and derivatives

As a theoretical component of the joint effort with the laboratory of Dr. Lou Allamandola to search for potential candidates for interstellar organic carbon compound that are responsible for the visible diffuse interstellar absorption bands (DIB's), quantum mechanical calculations were performed on the electron absorption spectra of selected polycyclic aromatic hydrocarbons (PAH) and derivatives. In the completed project, 15 different species of naphthalene, its hydrogen abstraction and addition derivatives, and corresponding cations and anions were studied. Using semiempirical quantum mechanical method INDO/S, the ground electronic state of each species was evaluated with restricted Hartree-Fock scheme and limited configuration interaction. The lowest energy spin state for each species was used for electron absorption calculations. Results indicate that these calculations are accurate enough to reproduce the spectra of naphthalene cation and anion observed in neon matrix. The spectral pattern of the hydrogen abstraction and addition derivatives predicted based on these results indicate that the electron configuration of the pi orbitals of these species is the dominant determinant. A combined list of 19 absorptions calculated from 4500 A to 10,400 A were compiled and suggested as potential candidates that are relevant for the DIB's absorptions. Continued studies on pyrene and derivatives revealed the ground state symmetries and multiplicities of its neutral, anionic, and cationic species. Spectral calculations show that the cation (B(sub 3g)-2) and the anion (A(sub u)-2) are more likely to have low energy absorptions in the regions between 10 kK and 20 kK, similar to naphthalene. These absorptions, together with those to be determined from the hydrogen abstraction and addition derivatives of pyrene, can be used to provide additional candidates and suggest experimental work in the search for interstellar compounds that are responsible for DIB's.

Du, Ping↗

Measuring the D/H Ratios of Exoplanets and Brown Dwarfs

The relative abundance of deuterium and hydrogen is a potent tracer of planet formation and evolution. Jupiter and Saturn have protosolar atmospheric D/H ratios, a relic of substantial gas accretion from the nebula, while the atmospheres of Neptune and Uranus are enhanced in D by accretion of ices into their envelopes. For terrestrial planets, D/H ratios are used to determine the mechanisms of volatile delivery and subsequent atmosphere loss over the lifetime of the planet. Planets and brown dwarfs more massive than ~13 M(J) quickly fuse their initial D reservoir. Here, we simulate spectra for giant exoplanets and brown dwarfs (2 M(Neptune) to ~10 M(Jupiter)) from T(eff) = 200–1800 K including both CH3D and HDO to determine the observability of these dominant deuterium isotopologues in mid-infrared thermal emission spectra. Colder objects have stronger molecular features in their spectra, due to the temperature dependence of molecular cross sections. CH3D is easier to observe than HDO at all temperatures considered, due to the strength of its absorption bands and locations of features at wavelengths with few other strong absorption features. We predict that for nearby cool brown dwarfs, the CH3D abundance can be measured at high signal to noise with the James Webb Space Telescope (JWST); for objects from 200 to 800 K closer than 10 pc, a protosolar D/H ratio would be readily observable in 2.5 hr. Moderately young Jupiter-mass planets (100–300 Myr) and young Neptunes (10 Myr) may be discovered with JWST and provide the best targets for detecting deuterium on an exoplanet in the coming decade. Future telescope designs should consider the importance of isotopes for understanding the formation and evolution of planetary atmospheres.

Caroline V. Morley↗

The infrared spectrum of the carbon star Y Canum Venaticorum between 1.2 and 30 microns

The paper deals with spectrophotometric observations covering the essentially complete wavelength interval between 1.2 and 30.0 microns. The observations confirm the identification of the C3 band at 5.2 microns. They show that if SiC2 is present, the SiC1 absorption band at 5.7 microns would be obscured by C3 at a 1% spectral resolution. Silicon carbide emission at 11.5 microns exists simultaneously with C3 absorption at 5.2 microns, requiring a contribution of both species to the violet opacity of Y CVn.

Goebel, J. H.↗

High-Resolution IR Absorption Spectroscopy of Polycyclic Aromatic Hydrocarbons in the 3-micrometers Region: Role of Periphery

In this work we report on high-resolution IR absorption studies that provide a detailed view on how the peripheral structure of irregular polycyclic aromatic hydrocarbons (PAHs) affects the shape and position of their 3-micrometers absorption band. To this purpose we present mass-selected, high-resolution absorption spectra of cold and isolated phenanthrene, pyrene, benz[a]antracene, chrysene, triphenylene, and perylene molecules in the 2950-3150 per cm range. The experimental spectra are compared with standard harmonic calculations, and anharmonic calculations using a modified version of the SPECTRO program that incorporates a Fermi resonance treatment utilizing intensity redistribution. We show that the 3-micrometers region is dominated by the effects of anharmonicity, resulting in many more bands than would have been expected in a purely harmonic approximation. Importantly, we find that anharmonic spectra as calculated by SPECTRO are in good agreement with the experimental spectra. Together with previously reported high-resolution spectra of linear acenes, the present spectra provide us with an extensive dataset of spectra of PAHs with a varying number of aromatic rings, with geometries that range from open to highly-condensed structures, and featuring CH groups in all possible edge configurations. We discuss the astrophysical implications of the comparison of these spectra on the interpretation of the appearance of the aromatic infrared 3-micrometers band, and on features such as the two-component emission character of this band and the 3-micrometers emission plateau.

techniques: spectroscopic↗

Titan's spectrum and atmospheric composition

Spectroscopic evidence shows that hydrogen atoms are major constituents of Titan's atmosphere. Anomalous enhancement of the methane absorption band is attributed to isotopic shifts arising from methane photolysis. Anomalous ultraviolet absorption features suggest high altitude dust and an elevated cloud layer overlaying most of the methane in the atmosphere.

Trafton, L. M.↗