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All sourcesNASA NTRSDOE OSTI
DOE OSTI2024

Weak Gravitational Lensing around Low Surface Brightness Galaxies in the DES Year 3 Data

We present galaxy-galaxy lensing measurements using a sample of low surface brightness galaxies (LSBGs) drawn from the Dark Energy Survey Year 3 (Y3) data as lenses. LSBGs are diffuse galaxies with a surface brightness dimmer than the ambient night sky. These dark-matter-dominated objects are intriguing due to potentially unusual formation channels that lead to their diffuse stellar component. Given the faintness of LSBGs, using standard observational techniques to characterize their total masses proves challenging. Weak gravitational lensing, which is less sensitive to the stellar component of galaxies, could be a promising avenue to estimate the masses of LSBGs. Our LSBG sample consists of 23,790 galaxies separated into red and blue color types at g - i ≥ 0.60 and g - i < 0.60 , respectively. Combined with the DES Y3 shear catalog, we measure the tangential shear around these LSBGs and find signal-to-noise ratios of 6.67 for the red sample, 2.17 for the blue sample, and 5.30 for the full sample. We use the clustering redshifts method to obtain redshift distributions for the red and blue LSBG samples. Assuming all red LSBGs are satellites, we fit a simple model to the measurements and estimate the host halo mass of these LSBGs to be log(M host /M ⊙ ) = $12.98^{+0.10}_{-0.11}$. We place a 95% upper bound on the subhalo mass at log(M sub /M ⊙ ) < 11.51. By contrast, we assume the blue LSBGs are centrals, and place a 95% upper bound on the halo mass at log(M host /M ⊙ ) < 11.84. We find that the stellar-to-halo mass ratio of the LSBG samples is consistent with that of the general galaxy population. This work illustrates the viability of using weak gravitational lensing to constrain the halo masses of LSBGs.

79 ASTRONOMY AND ASTROPHYSICS↗
DOE OSTI2025

Refining localtype primordial non-Gaussianity: Sharpened bϕ constraints through bias expansion

Local-type primordial non-Gaussianity (PNG), predicted by many nonminimal models of inflation, creates a scale-dependent contribution to the power spectrum of large-scale structure tracers. Its amplitude is characterized by the product bϕfNLloc, where bϕ is an astrophysical parameter dependent on the properties of the tracer. However, bϕ exhibits significant secondary dependence on halo concentration and other astrophysical properties, which may bias and weaken the constraints on fNLloc. In this work, we demonstrate that incorporating knowledge of the relation between Lagrangian bias parameters and bϕ can significantly enhance PNG constraints. We employ the hybrid effective field theory approach at the field level and a linear regression model to seek a connection between the bias parameters and bϕ for halo and galaxy samples, constructed using the abacussummit simulation suite and mimicking the luminous red galaxies and quasistellar objects of the Dark Energy Spectroscopic Instrument survey. For the fixed-mass halo samples, our full bias model reduces the uncertainty by more than 70%, with most of that improvement coming from b∇, which we find to be an excellent proxy for concentration. For the galaxy samples, our model reduces the uncertainty on bϕ by 80% for all tracers. By adopting Lagrangian-bias informed priors on the parameter bϕ, future analyses can thus constrain fNLloc with less bias and smaller errors.

Hadzhiyska, Boryana↗
DOE OSTI2026

Quiescent Host Galaxies of Extended Quasars Revealed by Spectrophotometric Decomposition

Previous works of low-redshift quasar host galaxies have focused on compact quasars and found that their host galaxies are mainly star-forming galaxies. Here, we present a study of host galaxies for quasars with extended morphologies in ground-based optical images. We select a sample of more than 1000 type 1 quasars at redshift 0.1 < z < 1 that are classified as extended objects by the Dark Energy Spectroscopic Instrument (DESI). Combining high-resolution spectra from DESI and high-quality images from Subaru Hyper Suprime-Cam, we develop a spectrophotometric decomposition technique to iteratively decompose each quasar into an active galactic nucleus (AGN) component and its host galaxy. The technique can effectively break the degeneracy between the AGN and host components and capture the host spectral features. Our results show that the host galaxies of most quasars have low star formation rates (SFRs) and low specific SFRs, indicating that they are quiescent galaxies. Many of them exhibit prominent post-starburst features with the existence of significant old stellar populations. These properties are quite different from the nature of compact quasars with star-forming host galaxies. In addition, the relation between the black hole mass and stellar mass for our sample is broadly consistent with the canonical local relations. This work is complementary to the previous studies and suggests that the host galaxies of low-redshift quasars are more diverse than was thought.

79 ASTRONOMY AND ASTROPHYSICS↗
NASA NTRS1987

A VLA gravitational lens survey

A VLA survey designed to detect gravitational lensing on sub-arc second and arc second scales is described, and preliminary results of radio data are presented. In particular, it is found that the density of matter in the form of a uniform comoving number density of 10 to the 11th - 10 to the 12th solar mass compact objects, luminous or dark, must be substantially less than the critical density. Data obtained for the radio source 1042+178 are briefly examined.

Hewitt, J. N.↗
NASA NTRS1989

Near-infrared photometry of the Galilean satellites

The present near-IR (2.2-, 3.8-, 4.8-micron) lightcurves and phase coefficients for the Galilean satellites notes the geometric albedo of Io to include volcanic emission at the two longer wavelengths, although no major outbursts were detected during the 1982-1983 period of these observations. The trend of decreasing albedo with increasing wavelength exhibited by Ganymede and Europa is consistent with their possession of icy surfaces. The results obtained for Callisto are consistent with visible-wavelength observations of other dark solar system objects.

Tittemore, William C.↗
NASA NTRS1990

Image segmentation by background extraction refinements

An image segmentation method refining background extraction in two phases is presented. In the first phase, the method detects homogeneous-background blocks and estimates the local background to be extracted throughout the image. A block is classified homogeneous if its left and right standard deviations are small. The second phase of the method refines background extraction in nonhomogeneous blocks by recomputing the shoulder thresholds. Rules that predict the final background extraction are derived by observing the behavior of successive background statistical measurements in the regions under the presence of dark and/or bright object pixels. Good results are shown for a number of outdoor scenes.

Rodriguez, Arturo A.↗
NASA NTRS1993

The Ultraviolet Plume Instrument (UVPI)

The Ultraviolet Plume Instrument (UVPI) was launched aboard the Low-power Atmospheric Compensation Experiment (LACE) satellite on 14 Feb. 1990. Both the spacecraft and the UVPI were sponsored by the Directed Energy Office of the Strategic Defense Initiative Organization. The mission of the UVPI was to obtain radiometrically calibrated images of rocket plumes at high altitude and background image data of the Earth, Earth's limb, and celestial objects in the near- and middle-UV wave bands. The UVPI was designed for nighttime observations, i.e., to acquire and track relatively bright objects against a dark background.

Horan, D. M.↗
NASA NTRS2004

Fluorescent Approaches to High Throughput Crystallography

X-ray crystallography remains the primary method for determining the structure of macromolecules. The first requirement is to have crystals, and obtaining them is often the rate-limiting step. The numbers of crystallization trials that are set up for any one protein for structural genomics, and the rate at which they are being set up, now overwhelm the ability for strictly human analysis of the results. Automated analysis methods are now being implemented with varying degrees of success, but these typically cannot reliably extract intermediate results. By covalently modifying a subpopulation, less than or = 1%, of a macromolecule solution with a fluorescent probe, the labeled material will add to a growing crystal as a microheterogeneous growth unit. Labeling procedures can be readily incorporated into the final stages of a macromolecules purification. The covalently attached probe will concentrate in the crystal relative to the solution, and under fluorescent illumination the crystals will show up as bright objects against a dark background. As crystalline packing is more dense than amorphous precipitate, the fluorescence intensity can be used as a guide in distinguishing different types of precipitated phases, even in the absence of obvious crystalline features, widening the available potential lead conditions in the absence of clear "bits." Non-protein structures, such as salt crystals, will not incorporate the probe and will not show up under fluorescent illumination. Also, brightly fluorescent crystals are readily found against less fluorescent precipitated phases, which under white light illumination may serve to obscure the crystals. Automated image analysis to find crystals should be greatly facilitated, without having to first define crystallization drop boundaries and by having the protein or protein structures all that show up. The trace fluorescently labeled crystals will also emit with sufficient intensity to aid in the automation of crystal alignment using relatively low cost optics, further increasing throughput at synchrotrons. This presentation will focus on the methodology for fluorescent labeling, the crystallization results, and the effects of the trace labeling on the crystal quality.

Minamitani, Elizabeth Forsythe↗
NASA NTRS2004

Fluorescent Approaches to High Throughput Crystallography

X-ray crystallography remains the primary method for determining the structure of macromolecules. The first requirement is to have crystals, and obtaining them is often the rate-limiting step. The numbers of crystallization trials that are set up for any one protein for structural genomics, and the rate at which they are being set up, now overwhelm the ability for strictly human analysis of the results. Automated analysis methods are now being implemented with varying degrees of success, but these typically can not reliably extract intermediate results. By covalently modifying a subpopulation, less than or = 1%, of a macromolecule solution with a fluorescent probe, the labeled material will add to a growing crystal as a microheterogeneous growth unit. Labeling procedures can be readily incorporated into the final stages of purification. The covalently attached probe will concentrate in the crystal relative to the solution, and under fluorescent illumination the crystals show up as bright objects against a dark background. As crystalline packing is more dense than amorphous precipitate, the fluorescence intensity can be used as a guide in distinguishing different types of precipitated phases, even in the absence of obvious crystalline features, widening the available potential lead conditions in the absence of clear "hits." Non-protein structures, such as salt crystals, will not incorporate the probe and will not show up under fluorescent illumination. Also, brightly fluorescent crystals are readily found against less fluorescent precipitated phases, which under white light illumination may serve to obscure the crystals. Automated image analysis to find crystals should be greatly facilitated, without having to first define crystallization drop boundaries and by having the protein or protein structures all that show up. The trace fluorescently labeled crystals will also emit with sufficient intensity to aid in the automation of crystal alignment using relatively low cost optics, further increasing throughput at synchrotrons. This presentation will focus on the methodology for fluorescent labeling, the crystallization results, and the effects of the trace labeling on the crystal quality.

Pusey, Marc L.↗
NASA NTRS2005

Fluorescent Approaches to High Throughput Crystallography

X-ray crystallography remains the primary method for determining the structure of macromolecules. The first requirement is to have crystals, and obtaining them is often the rate-limiting step. The numbers of crystallization trials that are set up for any one protein for structural genomics, and the rate at which they are being set up, now overwhelm the ability for strictly human analysis of the results. Automated analysis methods are now being implemented with varying degrees of success, but these typically cannot reliably extract intermediate results. By covalently modifying a subpopulation, 51%, of a macromolecule solution with a fluorescent probe, the labeled material will add to a growing crystal as a microheterogeneous growth unit. Labeling procedures can be readily incorporated into the final stages of purification. The covalently attached probe will concentrate in the crystal relative to the solution, and under fluorescent illumination the crystals show up as bright objects against a dark background. As crystalline packing is more dense than amorphous precipitate, the fluorescence intensity can be used as a guide in distinguishing different types of precipitated phases, even in the absence of obvious crystalline features, widening the available potential lead conditions in the absence of clear hits. Non-protein structures, such as salt crystals, will not incorporate the probe and will not show up under fluorescent illumination. Also, brightly fluorescent crystals are readily found against less fluorescent precipitated phases, which under white light illumination may serve to obscure the crystals. Automated image analysis to find crystals should be greatly facilitated, without having to first define crystallization drop boundaries and by having the protein or protein structures all that show up. The trace fluorescently labeled crystals will also emit with sufficient intensity to aid in the automation of crystal alignment using relatively low cost optics, further increasing throughput at synchrotrons. This presentation will focus on the methodology for fluorescent labeling, the crystallization results, and the effects of the trace labeling on the crystal quality.

Pusey, Marc L.↗
NASA NTRS2005

Fluorescent Approaches to High Throughput Crystallography

X-ray crystallography remains the primary method for determining the structure of macromolecules. The first requirement is to have crystals, and obtaining them is often the rate-limiting step. The numbers of crystallization trials that are set up for any one protein for structural genomics, and the rate at which they are being set up, now overwhelm the ability for strictly human analysis of the results. Automated analysis methods are now being implemented with varying degrees of success, but these typically cannot reliably extract intermediate results. By covalently modifying a subpopulation, less than or = 1 %, of a macromolecule solution with a fluorescent probe, the labeled material will add to a growing crystal as a microheterogeneous growth unit. Labeling procedures can be readily incorporated into the final stages of purification. The covalently attached probe will concentrate in the crystal relative to the solution, and under fluorescent illumination the crystals show up as bright objects against a dark background. As crystalline packing is more dense than amorphous precipitate, the fluorescence intensity can be used as a guide in distinguishing different types of precipitated phases, even in the absence of obvious crystalline features, widening the available potential lead conditions in the absence of clear "hits." Non-protein structures, such as salt crystals, will not incorporate the probe and will not show up under fluorescent illumination. Also, brightly fluorescent crystals are readily found against less fluorescent precipitated phases, which under white light illumination may serve to obscure the crystals. Automated image analysis to find crystals should be greatly facilitated, without having to first define crystallization drop boundaries and by having the protein or protein structures all that show up. The trace fluorescently labeled crystals will also emit with sufficient intensity to aid in the automation of crystal alignment using relatively low cost optics, further increasing throughput at synchrotrons. Preliminary experiments show that the presence of the fluorescent probe does not affect the nucleation process or the quality of the X-ray data obtained.

Pusey, Marc L.↗
NASA NTRS2006

Fluorescent Approaches to High Throughput Crystallography

We have shown that by covalently modifying a subpopulation, less than or equal to 1%, of a macromolecule with a fluorescent probe, the labeled material will add to a growing crystal as a microheterogeneous growth unit. Labeling procedures can be readily incorporated into the final stages of purification, and the presence of the probe at low concentrations does not affect the X-ray data quality or the crystallization behavior. The presence of the trace fluorescent label gives a number of advantages when used with high throughput crystallizations. The covalently attached probe will concentrate in the crystal relative to the solution, and under fluorescent illumination crystals show up as bright objects against a dark background. Non-protein structures, such as salt crystals, will not incorporate the probe and will not show up under fluorescent illumination. Brightly fluorescent crystals are readily found against less bright precipitated phases, which under white light illumination may obscure the crystals. Automated image analysis to find crystals should be greatly facilitated, without having to first define crystallization drop boundaries as the protein or protein structures is all that shows up. Fluorescence intensity is a faster search parameter, whether visually or by automated methods, than looking for crystalline features. We are now testing the use of high fluorescence intensity regions, in the absence of clear crystalline features or "hits", as a means for determining potential lead conditions. A working hypothesis is that kinetics leading to non-structured phases may overwhelm and trap more slowly formed ordered assemblies, which subsequently show up as regions of brighter fluorescence intensity. Preliminary experiments with test proteins have resulted in the extraction of a number of crystallization conditions from screening outcomes based solely on the presence of bright fluorescent regions. Subsequent experiments will test this approach using a wider range of proteins. The trace fluorescently labeled crystals will also emit with sufficient intensity to aid in the automation of crystal alignment using relatively low cost optics, further increasing throughput at synchrotrons.

Pusey, Marc L.↗
NASA NTRS2024

The dynamical origins of the dark comets and a proposed evolutionary track

So-called ‘dark comets’ are small, morphologically inactive near-Earth objects (NEOs) that exhibit nongravitational accelerations inconsistent with radiative effects. These objects exhibit short rotational periods (minutes to hours), where measured. We find that the strengths required to prevent catastrophic disintegration are consistent with those measured in cometary nuclei and expected in rubble pile objects. We hypothesize that these dark comets are the end result of a rotational fragmentation cascade, which is consistent with their measured physical properties. We calculate the predicted size-frequency distribution for objects evolving under this model. Using dynamical simulations, we further demonstrate that the majority of these bodies originated from the 𝜈6 resonance, implying the existence of volatiles in the current inner main belt. Moreover, one of the dark comets, (523599) 2003 RM, likely originated from the outer main belt, although a JFC origin is also plausible. These results provide strong evidence that volatiles from a reservoir in the inner main belt are present in the near-Earth environment.

Aster G Taylor↗
NASA NTRS1991

Infrared recombination lines of hydrogen from young objects in the southern Galactic plane

Near infrared recombination lines of hydrogen are observed in twelve young objects in the southern Galactic plane. The sample includes Herbig-Haro objects and IRAS dark-cloud point sources from the 1987 catalog of Persson and Campbell. In four of the IRAS sources two or three infrared lines are measured, and their intensity ratios are consistent with models of optically thick ionized winds. The intrinsic line shapes, retrieved from maximum-entropy deconvolutions, indicate gas velocities of 100 km/s or more as expected from ionized winds. These sources are apparently embedded pre-main-sequence objects with outflows. They include some of the brightest known YSOs.

Beck, Sara C.↗
NASA NTRS1990

Radiometric measurements of gap probability in conifer tree canopies

Measurements of gap probability were made for some moderate-sized, open-grown conifers of varying species. Results of the radiometric analysis show that the gap probability, which is taken as the mean of the binomial, fits well a negative exponential function of a path length. The conifer shadow, then, is an object of almost uniform darkness with some bright holes or gaps that are found near the shadow's edge and rapidly disappear toward the shadows center.

Albers, Bryan J.↗
NASA NTRS1995

A count probability cookbok: Spurious effects and the scaling model

We study the errors brought by finite volume effects and dilution effects on the practical determination of the count probability distribution function P(sub N)(n,l), which is the probability of having N objects in a cell of volume l cubed for a set of average number density n. Dilution effects are particularly revelant to the so-called sparse sampling strategy. This work is mainly done in the framework of the Bailan & Schaeffer scaling model, which assumes that the Q-body correlation functions obey the scaling relation Xi(sub Q)(lambda r(sub l),....lambda r(sub Q) = lambda(exp -(Q-1)gamma) Xi(sub Q)(r(sub 1),....r(sub Q)). We use three synthetic samples as references to perform our analysis: a fractal generated by a Rayleigh-Levy random walk with approximately 3 x 10(exp 4) objects, a sample dominated by a spherical power-law cluster with approximately 3 x 10(exp 4) objects and a cold dark matter (CDM) universe involving approximately 3 x 10(exp 5) matter particles.

Colombi, S.↗
NASA NTRS1988

Astrometric observations of asteroids and small bodies

Comets and asteroids are observed with the Palomar 1.5 m telescope using a charge coupled device (CCD) array. The goal is observations of astrometric quality (the reduction to position is separately funded) and the priorities are comets plus minor planets which are planet crossers, have high inclinations, or otherwise have unusual orbits. The stress is on recoveries of comets and asteroids seen at previous oppositions and follow up on newly discovered objects. Surveys and new discoveries are not being attempted. The modest amount of available dark time is used for faint objects, while brighter objects can be followed in the more plentiful light time. Since asteroids are usually discovered near perihelion when bright, the next several opportunities for recovery are normallly fainter. Thus recoveries and follow up with big telescopes complement surveys by smaller instruments. During the past year two periodic comets were recovered. They were P/Jackson-Neujmin (1987t) and P/Longmore (1987c1). Both were shared recoveries. A follow up observation of the newly-discovered comet Rudenko (1987u) appeared on an IAU card as did the newly discovered Comet Maury-Phinney (1988c). A magnitude 14.4 outburst of comet Schwassmann-Wachmann 1 was recorded at the end of May and was reported on an IAU card.

Williams, James G.↗