The Ellipticity of the Disks of Spiral Galaxies

The disks of spiral galaxies are generally elliptical rather than circular. The distribution of ellipticities can be fit with a log-normal distribution. For a sample of 12,764 galaxies from the Sloan Digital Sky Survey Data Release 1 (SDSS DR1), the distribution of apparent axis ratios in the i band is best fit by a log-normal distribution of intrinsic ellipticities with ln epsilon = -1.85 +/- 0.89. For a sample of nearly face-on spiral galaxies, analyzed by Andersen and Bershady using both photometric and spectroscopic data, the best fitting distribution of ellipticities has ln epsilon = -2.29 +/- 1.04. Given the small size of the Andersen-Bershady sample, the two distribution are not necessarily inconsistent. If the ellipticity of the potential were equal to that of the light distribution of the SDSS DR1 galaxies, it would produce 1.0 magnitudes of scatter in the Tully-Fisher relation, greater than is observed. The Andersen-Bershady results, however, are consistent with a scatter as small as 0.25 magnitudes in the Tully-Fisher relation.Comment: 19 pages, 5 figures; ApJ, accepte

A Comparison of the Intrinsic Shapes of Two Different Types of Dwarf Galaxies: Blues Compact Dwarfs and Dwarf Ellipticals

We measure the apparent shapes for a sample of 62 blue compact dwarf galaxies (BCDs), and compare them with the apparent shapes for a sample of 80 dwarf elliptical galaxies (dEs). The BCDs are flatter, on average, than the dEs, but the difference is only marginally significant. We then use both non-parametric and parametric techniques to determine possible distributions of intrinsic shapes for the BCDs. The hypothesis that BCDs are oblate spheroids can be ruled out with a high confidence level ($> 99$), but the hypothesis that they are prolate spheroids cannot be excluded. The apparent shapes of BCDs are totally consistent with the hypothesis that they are triaxial ellipsoids. If the intrinsic axis ratios, $\beta$ and $\gamma$, are distributed according to a Gaussian with means $\beta_0$ and $\gamma_0$ and standard deviation $\sigma$, we find the best-fitting distribution for BCDs has $(\beta_0,\gamma_0,\sigma)= (0.66,0.55,0.16)$, while that for dEs has $(\beta_0,\gamma_0,\sigma)= (0.85,0.64,0.24)$. Our results are consistent with the hypothesis that BCDs have a close evolutionary relation with dEs.Comment: total 23 pages, 9 figures, and 1 Table, submitted to ApJ on Sep 19 1997. Email addresses: [email protected], [email protected], [email protected], [email protected], [email protected]

The Intrinsic Shape of Spiral Galaxies in the 2MASS Large Galaxy Atlas

The apparent shapes of spiral galaxies in the 2-Micron All Sky Survey Large Galaxy Atlas are used to constrain the intrinsic shape of their disks. When the distribution of apparent axis ratios is estimated using a nonparametric kernel method, the shape distribution is inconsistent with axisymmetry at the 90% confidence level in the B band and at the 99% confidence level in the K band. If spirals are subdivided by Hubble type, the late-type spirals (Sc and later) are consistent with axisymmetry, while the earlier spirals are strongly inconsistent with axisymmetry. The distribution of disk ellipticity can be fitted adequately with either a Gaussian or a lognormal distribution. The best fits for the late spirals imply a median ellipticity of epsilon = 0.07 in the B band and epsilon = 0.02 in the K band. For the earlier spirals, the best fits imply a median ellipticity of epsilon = 0.18 in the B band and epsilon = 0.30 in the K band. The observed scatter in the Tully-Fisher relation, for both late and early spirals, is consistent with the disk ellipticity measured in the B band. This indicates that excluding spirals of Hubble type earlier than Sc will reduce the intrinsic scatter in the Tully-Fisher relation used as a distance indicator.Comment: 30 pages, 9 figures, to appear in Ap

Genomic analysis of the population structure of Paenibacillus larvae in New Zealand

New Zealand is a remote country in the South Pacific Ocean. The isolation and relatively late arrival of humans into New Zealand has meant there is a recorded history of the introduction of domestic species. Honey bees (Apis mellifera) were introduced to New Zealand in 1839, and the disease American foulbrood was subsequently found in the 1870s. Paenibacillus larvae, the causative agent of American foulbrood, has been genome sequenced in other countries. We sequenced the genomes of P. larvae obtained from 164 New Zealand apiaries where American foulbrood was identified in symptomatic hives during visual inspection. Multi-locus sequencing typing (MLST) revealed the dominant sequence type to be ST18, with this clonal cluster accounting for 90.2% of isolates. Only two other sequence types (with variants) were identified, ST5 and ST23. ST23 was only observed in the Otago area, whereas ST5 was limited to two geographically non-contiguous areas. The sequence types are all from the enterobacterial repetitive intergenic consensus I (ERIC I) genogroup. The ST18 and ST5 from New Zealand and international P. larvae all clustered by sequence type. Based on core genome MLST and SNP analysis, localized regional clusters were observed within New Zealand, but some closely related genomes were also geographically dispersed, presumably due to hive movements by beekeepers

Glacial Refugia in Pathogens: European Genetic Structure of Anther Smut Pathogens on Silene latifolia and Silene dioica

Climate warming is predicted to increase the frequency of invasions by pathogens and to cause the large-scale redistribution of native host species, with dramatic consequences on the health of domesticated and wild populations of plants and animals. The study of historic range shifts in response to climate change, such as during interglacial cycles, can help in the prediction of the routes and dynamics of infectious diseases during the impending ecosystem changes. Here we studied the population structure in Europe of two Microbotryum species causing anther smut disease on the plants Silene latifolia and Silene dioica. Clustering analyses revealed the existence of genetically distinct groups for the pathogen on S. latifolia, providing a clear-cut example of European phylogeography reflecting recolonization from southern refugia after glaciation. The pathogen genetic structure was congruent with the genetic structure of its host species S. latifolia, suggesting dependence of the migration pathway of the anther smut fungus on its host. The fungus, however, appeared to have persisted in more numerous and smaller refugia than its host and to have experienced fewer events of large-scale dispersal. The anther smut pathogen on S. dioica also showed a strong phylogeographic structure that might be related to more northern glacial refugia. Differences in host ecology probably played a role in these differences in the pathogen population structure. Very high selfing rates were inferred in both fungal species, explaining the low levels of admixture between the genetic clusters. The systems studied here indicate that migration patterns caused by climate change can be expected to include pathogen invasions that follow the redistribution of their host species at continental scales, but also that the recolonization by pathogens is not simply a mirror of their hosts, even for obligate biotrophs, and that the ecology of hosts and pathogen mating systems likely affects recolonization patterns

Image_1_Genomic analysis of the population structure of Paenibacillus larvae in New Zealand.TIF

New Zealand is a remote country in the South Pacific Ocean. The isolation and relatively late arrival of humans into New Zealand has meant there is a recorded history of the introduction of domestic species. Honey bees (Apis mellifera) were introduced to New Zealand in 1839, and the disease American foulbrood was subsequently found in the 1870s. Paenibacillus larvae, the causative agent of American foulbrood, has been genome sequenced in other countries. We sequenced the genomes of P. larvae obtained from 164 New Zealand apiaries where American foulbrood was identified in symptomatic hives during visual inspection. Multi-locus sequencing typing (MLST) revealed the dominant sequence type to be ST18, with this clonal cluster accounting for 90.2% of isolates. Only two other sequence types (with variants) were identified, ST5 and ST23. ST23 was only observed in the Otago area, whereas ST5 was limited to two geographically non-contiguous areas. The sequence types are all from the enterobacterial repetitive intergenic consensus I (ERIC I) genogroup. The ST18 and ST5 from New Zealand and international P. larvae all clustered by sequence type. Based on core genome MLST and SNP analysis, localized regional clusters were observed within New Zealand, but some closely related genomes were also geographically dispersed, presumably due to hive movements by beekeepers.</p