The Ages of Elliptical Galaxies in a Merger Model

The tightness of the observed colour-magnitude and Mg$_{2}$- velocity dispersion relations for elliptical galaxies has often been cited as an argument against a picture in which ellipticals form by the merging of spiral disks. A common view is that merging would mix together stars of disparate ages and produce a large scatter in these relations. Here I use semi-analytic models of galaxy formation to derive the distribution of the mean ages, colours and metallicities of the stars in elliptical galaxies formed by mergers in a flat CDM universe. It is seen that most of the stars in ellipticals form at relatively high redshift (z > 1.9) and that the predicted scatter in the colour-magnitude and Mg_2 - sigma relations falls within observational bounds. I conclude that the apparent homogeneity in the properties of the stellar populations of ellipticals is not inconsistent with a merger scenario for the origin of these systems.Comment: latex file, figures available upon reques

The Evolving Faint-End of the Luminosity Function

We investigate the evolution of the faint-end slope of the luminosity function, $\alpha$, using semi-analytical modeling of galaxy formation. In agreement with observations, we find that the slope can be fitted well by $\alpha (z) =a+b z$, with a=-1.13 and b=-0.1. The main driver for the evolution in $\alpha$ is the evolution in the underlying dark matter mass function. Sub-L_* galaxies reside in dark matter halos that occupy a different part of the mass function. At high redshifts, this part of the mass function is steeper than at low redshifts and hence $\alpha$ is steeper. Supernova feedback in general causes the same relative flattening with respect to the dark matter mass function. The faint-end slope at low redshifts is dominated by field galaxies and at high redshifts by cluster galaxies. The evolution of $\alpha(z)$ in each of these environments is different, with field galaxies having a slope b=-0.14 and cluster galaxies b=-0.05. The transition from cluster-dominated to field-dominated faint-end slope occurs roughly at a redshift $z_* \sim 2$, and suggests that a single linear fit to the overall evolution of $\alpha(z)$ might not be appropriate. Furthermore, this result indicates that tidal disruption of dwarf galaxies in clusters cannot play a significant role in explaining the evolution of $\alpha(z)$ at z< z_*. In addition we find that different star formation efficiencies a_* in the Schmidt-Kennicutt-law and supernovae-feedback efficiencies $\epsilon$ generally do not strongly influence the evolution of $\alpha(z)$.Comment: 4 pages, replaced with version accepted to ApJL, minor changes to figure

Decarboxylation of Carbon Compounds as a Potential Source for CO2 and CO Observed by SAM at Yellowknife Bay, Gale Crater, Mars

Martian carbon was detected in the Sheepbed mudtsone at Yellowknife Bay, Gale Crater, Mars by the Sample Analysis at Mars (SAM) instrument onboard Curiosity, the rover of the Mars Science Laboratory missio]. The carbon was detected as CO2 thermally evolved from drilled and sieved rock powder that was delivered to SAM as a <150-micron-particle- size fraction. Most of the CO2 observed in the Cumberland (CB) drill hole evolved between 150deg and 350deg C. In the John Klein (JK) drill hole, the CO2 evolved up to 500deg C. Hypotheses for the source of the the CO2 include the breakdown of carbonate minerals reacting with HCl released from oxychlorine compounds, combustion of organic matter by O2 thermally evolved from the same oxychlorine minerals, and the decarboxylation of organic molecules indigenous to the martian rock sample. Here we explore the potential for the decarboxylation hypothesis

Evolution since z = 0.5 of the Morphology-Density relation for Clusters of Galaxies

Using traditional morphological classifications of galaxies in 10 intermediate-redshift (z~0.5) clusters observed with WFPC-2 on the Hubble Space Telescope, we derive relations between morphology and local galaxy density similar to that found by Dressler for low-redshift clusters. Taken collectively, the `morphology-density' relationship, M-D, for these more distant, presumably younger clusters is qualitatively similar to that found for the local sample, but a detailed comparison shows two substantial differences: (1) For the clusters in our sample, the M-D relation is strong in centrally concentrated ``regular'' clusters, those with a strong correlation of radius and surface density, but nearly absent for clusters that are less concentrated and irregular, in contrast to the situation for low redshift clusters where a strong relation has been found for both. (2) In every cluster the fraction of elliptical galaxies is as large or larger than in low-redshift clusters, but the S0 fraction is 2-3 times smaller, with a proportional increase of the spiral fraction. Straightforward, though probably not unique, interpretations of these observations are (1) morphological segregation proceeds hierarchically, affecting richer, denser groups of galaxies earlier, and (2) the formation of elliptical galaxies predates the formation of rich clusters, and occurs instead in the loose-group phase or even earlier, but S0's are generated in large numbers only after cluster virialization.Comment: 35 pages, 19 figures, uses psfig. Accepted for publication in Ap

Cytoplasmic Dynein Heavy Chain 1b Is Required for Flagellar Assembly in Chlamydomonas

A second cytoplasmic dynein heavy chain (cDhc) has recently been identified in several organisms, and its expression pattern is consistent with a possible role in axoneme assembly. We have used a genetic approach to ask whether cDhc1b is involved in flagellar assembly in Chlamydomonas. Using a modified PCR protocol, we recovered two cDhc sequences distinct from the axonemal Dhc sequences identified previously. cDhc1a is closely related to the major cytoplasmic Dhc, whereas cDhc1b is closely related to the minor cDhc isoform identified in sea urchins, Caenorhabditis elegans, and Tetrahymena. TheChlamydomonas cDhc1b transcript is a low-abundance mRNA whose expression is enhanced by deflagellation. To determine its role in flagellar assembly, we screened a collection of stumpy flagellar (stf) mutants generated by insertional mutagenesis and identified two strains in which portions of the cDhc1bgene have been deleted. The two mutants assemble short flagellar stumps (<1–2 μm) filled with aberrant microtubules, raft-like particles, and other amorphous material. The results indicate that cDhc1b is involved in the transport of components required for flagellar assembly in Chlamydomonas

Example Based Learning for View-Based Human Face Detection

We present an example-based learning approach for locating vertical frontal views of human faces in complex scenes. The technique models the distribution of human face patterns by means of a few view-based "face'' and "non-face'' prototype clusters. At each image location, the local pattern is matched against the distribution-based model, and a trained classifier determines, based on the local difference measurements, whether or not a human face exists at the current image location. We provide an analysis that helps identify the critical components of our system