scholarly journals Discriminating between hazy and clear hot-Jupiter atmospheres with CARMENES

2020 ◽  
Vol 643 ◽  
pp. A24
Author(s):  
A. Sánchez-López ◽  
M. López-Puertas ◽  
I. A. G. Snellen ◽  
E. Nagel ◽  
F. F. Bauer ◽  
...  

Context. Relatively large radii of some hot Jupiters observed in the ultraviolet and blue-optical are generally interpreted to be due to Rayleigh scattering by high-altitude haze particles. However, the haze composition and its production mechanisms are not fully understood, and observational information is still limited. Aims. We aim to study the presence of hazes in the atmospheres of HD 209458 b and HD 189733 b with high spectral resolution spectra by analysing the strength of water vapour cross-correlation signals across the red optical and near-infrared wavelength ranges. Methods. A total of seven transits of the two planets were observed with the CARMENES spectrograph at the 3.5 m Calar Alto telescope. Their Doppler-shifted signals were disentangled from the telluric and stellar contributions using the detrending algorithm SYSREM. The residual spectra were subsequently cross-correlated with water vapour templates at 0.70–0.96 μm to measure the strength of the water vapour absorption bands. Results. The optical water vapour bands were detected at 5.2σ in HD 209458 b in one transit, whereas no evidence of them was found in four transits of HD 189733 b. Therefore, the relative strength of the optical water bands compared to those in the near-infrared were found to be larger in HD 209458 b than in HD 189733 b. Conclusions. We interpret the non-detection of optical water bands in the transmission spectra of HD 189733 b, compared to the detection in HD 209458 b, to be due to the presence of high-altitude hazes in the former planet, which are largely absent in the latter. This is consistent with previous measurements with the Hubble Space Telescope. We show that currently available CARMENES observations of hot Jupiters can be used to investigate the presence of haze extinction in their atmospheres.

2015 ◽  
Vol 8 (6) ◽  
pp. 5895-5936 ◽  
Author(s):  
J. Lampel ◽  
D. Pöhler ◽  
J. Tschritter ◽  
U. Frieß ◽  
U. Platt

Abstract. In recent updates of the HITRAN water vapour H2O spectroscopic compilation covering the blue spectral region (here: 394–480 nm) significant changes for the absorption bands at 416 and 426 nm were reported. In order to investigate the consistency of the different cross-sections calculated from these compilations, H2O vapour column density ratios for different spectral intervals were retrieved from Long-path and Multi-Axis – Differential Optical Absorption Spectroscopy (DOAS) measurements. We observed a significant improvement of the DOAS evaluation when using the updated HITRAN water vapour absorption cross-sections for the calculation of the reference spectra. In particular the magnitudes of the residual spectra as well as the fit errors were reduced. However we also found that the best match between measurement and model is reached when the absorption cross-section of groups of lines are scaled by factors ranging from 0.5 and 1.9, suggesting that the HITRAN water vapour absorption compilation still needs significant corrections. For this spectral region we present correction factors for HITRAN 2009, HITRAN 2012, HITEMP and BT2 derived from field measurements. Additionally, upper limits for water vapour absorption in the UV-A range from 330–390 nm are given.


1997 ◽  
Vol 5 (3) ◽  
pp. 123-133 ◽  
Author(s):  
Céline Ventura ◽  
Marie Papini

The present study concerns diffuse reflectance spectroscopy of polymer powders and of their binary mixtures with inorganic materials. The total near-normal hemispherical spectral reflectance R of granular materials was measured in the near infrared wavelength range with a dispersive spectrophotometer. The measurement of the reflectance illustrated the influence of different parameters by taking into account (a) the morphology: powders or pellets and (b) the optical property of the material: semi-transparent, opaque or reflecting powders. The statistical treatment of the reflectance data by principal component analysis (PCA) allowed these data to be displayed in a reduced dimensionality space. As a result, the clustering of samples related to their chemical or their physical nature was carried out, giving a simpler description of the data in a new representation. The cross-correlation analysis of the reflectance values allowed similarities between absorption bands to be highlighted.


2020 ◽  
Vol 498 (1) ◽  
pp. 1023-1033
Author(s):  
E Keles ◽  
D Kitzmann ◽  
M Mallonn ◽  
X Alexoudi ◽  
L Fossati ◽  
...  

ABSTRACT High spectral resolution transmission spectroscopy is a powerful tool to characterize exoplanet atmospheres. Especially for hot Jupiters, this technique is highly relevant, due to their high-altitude absorption, e.g. from resonant sodium (Na i) and potassium (K i) lines. We resolve the atmospheric K i absorption on HD189733b with the aim to compare the resolved K i line and previously obtained high-resolution Na i-D line observations with synthetic transmission spectra. The line profiles suggest atmospheric processes leading to a line broadening of the order of ∼10 km/s for the Na i-D lines and only a few km/s for the K i line. The investigation hints that either the atmosphere of HD189733b lacks a significant amount of K i or the alkali lines probe different atmospheric regions with different temperature, which could explain the differences we see in the resolved absorption lines.


2015 ◽  
Vol 8 (10) ◽  
pp. 4329-4346 ◽  
Author(s):  
J. Lampel ◽  
D. Pöhler ◽  
J. Tschritter ◽  
U. Frieß ◽  
U. Platt

Abstract. In recent updates of the HITRAN water vapour H2O spectroscopic compilation covering the blue spectral region (here: 394–480 nm) significant changes for the absorption bands at 416 and 426 nm were reported. In order to investigate the consistency of the different cross-sections calculated from these compilations, H2O vapour column density ratios for different spectral intervals were retrieved from long-path and multi-axis differential optical absorption spectroscopy (DOAS) measurements. We observed a significant improvement of the DOAS evaluation when using the updated HITRAN water vapour absorption cross-sections for the calculation of the reference spectra. In particular the magnitudes of the residual spectra as well as the fit errors were reduced. However, we also found that the best match between measurement and model is reached when the absorption cross-section of groups of lines are scaled by factors ranging from 0.5 to 1.9, suggesting that the HITRAN water vapour absorption compilation still needs significant corrections. For this spectral region we present correction factors for HITRAN 2009, HITRAN 2012, HITEMP and BT2 derived from field measurements. Additionally, upper limits for water vapour absorption in the UV-A range from 330 to 390 nm are given.


2021 ◽  
Vol 13 (22) ◽  
pp. 4702
Author(s):  
Marcel Hess ◽  
Thorsten Wilhelm ◽  
Christian Wöhler ◽  
Kay Wohlfarth

On the Moon, in the near infrared wavelength range, spectral diagnostic features such as the 1-μm and 2-μm absorption bands can be used to estimate abundances of the constituent minerals. However, there are several factors that can darken the overall spectrum and dampen the absorption bands. Namely, (1) space weathering, (2) grain size, (3) porosity, and (4) mineral darkening agents such as ilmenite have similar effects on the measured spectrum. This makes spectral unmixing on the Moon a particularly challenging task. Here, we try to model the influence of space weathering and mineral darkening agents and infer the uncertainties introduced by these factors using a Markov Chain Monte Carlo method. Laboratory and synthetic mixtures can successfully be characterized by this approach. We find that the abundance of ilmenite, plagioclase, clino-pyroxenes and olivine cannot be inferred accurately without additional knowledge for very mature spectra. The Bayesian approach to spectral unmixing enables us to include prior knowledge in the problem without imposing hard constraints. Other data sources, such as gamma-ray spectroscopy, can contribute valuable information about the elemental abundances. We here find that setting a prior on TiO2 and Al2O3 can mitigate many of the uncertainties, but large uncertainties still remain for dark mature lunar spectra. This illustrates that spectral unmixing on the Moon is an ill posed problem and that probabilistic methods are important tools that provide information about the uncertainties, that, in turn, help to interpret the results and their reliability.


2020 ◽  
Author(s):  
Seiko Takagi

<p>The Venus cloud consists of a main cloud deck at 47 – 70 km, with thinner hazes above and below. The upper haze on Venus lies above the main cloud surrounding the planet, ranging from the cloud top (70 km) up to as high as 90 km.</p> <p>The Solar Occultation in the InfraRed (SOIR) instrument onboard Venus Express (ESA) was designed to measure the Venusian atmospheric transmission at high altitudes (65 – 220 km) in the infrared wavelength range (2.2 – 4.3 µm) with a high spectral resolution. In Takagi et al. (2019), the optical properties of Venus’s haze layer above 90 km have been investigated using SOIR observations. Vertical and latitudinal profiles of the extinction coefficient, optical thickness, and mixing ratio of aerosols are retrieved.</p> <p>A new cloud model was constructed based on the results of Takagi et al. (2019). In this presentation, I will show the results of a radiative transfer calculation (in the near-infrared region) that incorporates a new cloud model and discuss themeteorological some changes that contribute to cloud variation. Furthermore, I will introduce Venus observation plan using the 1.6 m Pirka telescope and Multi-Spectral Imager (MSI) [Watanabe et al., 2012] mounted on the Cassegrain focus of the telescope at the Nayoro Observatory of Hokkaido University.</p>


2005 ◽  
Vol 59 (4) ◽  
pp. 496-504 ◽  
Author(s):  
Steven J. Choquette ◽  
David L. Duewer ◽  
Leonard M. Hanssen ◽  
Edward A. Early

Standard Reference Material 2036 (SRM 2036) is a certified transfer standard intended for the verification and calibration of the wavelength/wavenumber scale of near-infrared (NIR) spectrometers operating in diffuse or trans-reflectance mode. SRM 2036 Near-Infrared Wavelength/Wavenumber Reflection Standard is a combination of a rare earth oxide glass of a composition similar to that of SRM 2035 Near-Infrared Transmission Wavelength/Wavenumber Standard and SRM 2065 Ultraviolet–Visible–Near-Infrared Transmission Wavelength/Wavenumber Standard, but is in physical contact with a piece of sintered poly(tetrafluoroethylene) (PTFE). The combination of glass contacted with a nearly ideal diffusely reflecting backing provides reflection–absorption bands that range from 15% R to 40% R. SRM 2036 is certified for the 10% band fraction air wavelength centroid location, 10%B, of seven bands spanning the spectral region from 975 nm to 1946 nm. It is also certified for the vacuum wavenumber 10%B of the same seven bands in the spectral region from 10 300 cm−1 to 5130 cm−1 at 8 cm−1 resolution. Informational values are provided for the locations of thirteen additional bands from 334 nm to 804 nm.


2020 ◽  
Author(s):  
Bernhard Jost ◽  
Paul V. Johnson ◽  
Robert Hodyss

<p><strong>Introduction:</strong> The analysis of evaporites on Europa’s surface will remain the only way to probe its subsurface ocean in near future. The ocean composition, and therefore potential habitability, is assumed to be driven by geophysical/chemical processes on the seafloor.</p> <p>Contrary to previous assumptions, recent observations indicate that chloride salts – rather than sulfate salts - could be Europa’s most abundant non-ice surface species. Nevertheless direct evidence of salt species has been largely inconclusive.</p> <p>The main problem in detecting salts is their spectral nature: most species are spectrally neutral across the visible and infrared wavelength range. The search has therefore to be concentrated on hydrated or radiolytic altered states of minerals.</p> <p>The presence of hydrated salt minerals was proposed after the Galileo mission [1]. Hydrated states of salts usually display characteristic absorption features in the near- and mid IR range. The same is true for Raman scattering.</p> <p>The only hint to the presence of salts in the visible range is the formation of color centers: a crystallographic defect where anionic vacancies are replaced by unpaired electrons, which leads to specific absorption bands. [2] suggested this mechanism as an alternative explanation for Europa's surface coloration, rather than sulfur chemistry.</p> <p>This work will provide the means to interpret the data acquired by future missions to icy worlds such as Europa Clipper and JUICE. Sodium chloride on Europa’s surface may be directly and unambiguously identified, if the characteristic spectral features of hydrohalite or color centers were observed. If features of hydrohalite were found, they would indicate a relatively young terrain.</p> <p><strong>Methods:</strong> We selected sodium chloride dehydrate (hydrohalite; NaCl◦2H<sub>2</sub>O) as candidate material for our study since it is the only stable hydrated state of sodium chloride under Europa conditions and NaCl has been proposed to relatively abundant on Europa. Hydrohalite forms below -0.15°C under varied conditions of NaCl concentrations and water activity.</p> <p>To analyze the hydration state of hydrohalite samples at JPL we use a combination of two different, but complementary techniques: 1. Passive near-infrared reflectance spectroscopy in the 1.4-7.0μm spectral range (Thermo Nicolet 6700 FTIR; Pike Tech DiffusIR) 2. Raman spectroscopy (Horiba Jobin-Yvon LabRam HR). The sample is irradiated using a krypton arc lamp primarily emitting at 116.5 and 123.6nm, however the 116.5nm line is cutoff by the MgF<sub>2</sub> window.</p> <p><strong>Results: </strong>Comparison studies show that the freezing rates of NaCl-brines play a crucial role in hydrohalite formation efficiency. Flash frozen droplets contain a significant lower concentration of hydrohalite than slowly frozen slabs. This finding might be important when comparing exposition scenarios on Europa such as vapour driven plumes or effusive flows.</p> <p>By freezing a saturated brine volume, the hydrohalite crystals are embedded within the ice matrix. Initially the ice suppresses the dehydration process. Only when the ice starts to sublimate at the surface, the non-ice component forms a residue layer of pure hydrohalite, which starts to dehydrate.</p> <p>The formation of color centers has, so far, been observed by UV irradiation and electron irradiation. However, timescales, necessary doses and penetration depth are different.<strong> </strong></p> <p><strong>References:</strong></p> <p>[1] McCord, T.B., et al.: Non-water-ice constituents in the surface material of the icy Galilean satellites from the Galileo near-infrared mapping spectrometer investigation. J. Geophys. Res. 103, pp. 8603-8626, 1998.</p> <p>[2] Hand, K.P. & Carlson, R.W.: Europa's surface color suggests an ocean rich with sodium chloride. Geophys. Res. Lett. 42, p. 3174-3178, 2015.</p>


The infra-red solar spectrum has been the subject of a fairly continuous study since the first elementary observations of Sir John Herschel in 1832. Figure 12 reproduces the solar spectrum recorded by Langley & Abbott in 1900, and this early record serves as an example to show that much of the sun’s incident energy fails to reach the earth. The main absorbing constituents of the atmosphere are water vapour and CO 2 , and these are the cause of the deep bands in the infra-red spectrum. In recent years other rearr gases, such as O 3 , HDO, CO, CH 4 and N 2 O, have been identified through their characteristic absorption bands. It is interesting to note that the HDO absorption band at 3·67 μ , first reported by Gebbie, Harding, Hilsum & Roberts in 1949, is clearly recorded in the Langley & Abbott spectrum, although with deuterium unknown it was impossible for them to identify it. The rarer constituents of the atmosphere have interested a number of experi­menters in more recent years and, for example, Shaw, Chapman, Howard & Oxholm (1951) have identified some 800 lines of atmphoseric origin in the small region between 3·0 and 5·2 μ . However, at ground level measurements are only possible where some solar energy reaches the earth. In order to make observations in the regions normally obscured it is necessary to reduce the amount of water vapour and carbon dioxide in the path by going to high altitude. The percentage CO 2 content of the atmosphere is approximately constant, and hence the amount of CO 2 between the sun and an observer will be reduced to one-half in going to 18000 ft. and to about one-tenth in going to 50000 ft. The water-vapour content falls off much more rapidly and measurements can be made in the 2·5 to 3·5 μ band by going to only 30000 ft. Migeotte & Neven (1952 a, b ) have made an attempt to overcome the effects of the denser lower atmosphere by making observations from the summit of the Jungfraujoch at a height of almost 12000 ft. By carrying a spectrometer in a modern aircraft it is possible to make detailed observations from heights greater than 50000 ft. A program of high-altitude spectroscopy is being undertaken jointly by the Gassiot Committee of the Royal Society and the Royal Aircraft Establishment, Farnborough. The purpose of the program is to record the solar spectrum out into the far infra-red from a Canberra aircraft flying at these heights.


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