Tracing ancient evolutionary divergence in parasites

For parasitic platyhelminths that generally lack a fossil record, there is little information on the pathways of morphological change during evolution. Polystomatid monogeneans are notable for their evolutionary diversification, having originated from ancestors on fish and radiated in parallel with tetrapod vertebrates over more than 425 million years. This study focuses on the genus Polystomoides that occurs almost worldwide on freshwater chelonian reptiles. Morphometric data show a major divergence in structural adaptations for attachment; this correlates with a dichotomy in micro-environmental conditions in habitats within the hosts. Species infecting the urinary tract have attachment organs with large hamuli and small suckers; species in the oro-nasal tract differ fundamentally, having small hamuli and large suckers. Zoogeographical and molecular evidence supports ancient separation of these site-specific clades: a new genus is proposed – Uropolystomoides – containing urinary tract species distinct from Polystomoides sensu stricto in oro-nasal sites. Aside from differences in attachment adaptations, body plans have probably changed little over perhaps 150 million years. This case contrasts markedly with polystomatids in other vertebrate groups where major morphological changes have evolved over much shorter timescales; the chelonian parasites show highly stable morphology across their global distribution over a long period of evolution, exemplifying ‘living fossils’

Environmental constraints influencing survival of an African parasite in a north temperate habitat: effects of temperature on development within the host

The monogenean Protopolystoma xenopodis has been established in Wales for >40 years following introduction with Xenopus laevis from South Africa. This provides an experimental system for determining constraints affecting introduced species in novel environments. Parasite development post-infection was followed at 15, 20 and 25 °C for 15 weeks and at 10 °C for51 year and correlated with temperatures recorded inWales. Development was slowed/arrested at410 °C which reflects habitat conditions for >6 months/year. There was wide variation in growth at constant temperature (body size differing by >10 times) potentially attributable in part to genotype-specific host-parasite interactions. Parasite density had no effect on size but host sex did: worms in males were 1·8 times larger than in females. Minimum time to patency was 51 days at 25 °C and 73 days at 20 °C although some infections were still not patent at both temperatures by 105 days p.i. In Wales, fastest developing infections may mature within one summer (about 12 weeks), possibly accelerated by movements of hosts into warmer surface waters. Otherwise, development slows/stops in October–April, delaying patency to about 1 year p.i., while wide variation in developmental rates may impose delays of 2 years in some primary infections and even longer in secondary infections

Environmental constraints influencing survival of an African parasite in a north temperate habitat: effects of temperature on egg development

SUMMARYFactors affecting survival of parasites introduced to new geographical regions include changes in environmental temperature. Protopolystoma xenopodis is a monogenean introduced with the amphibian Xenopus laevis from South Africa to Wales (probably in the 1960s) where low water temperatures impose major constraints on life-cycle processes. Effects were quantified by maintenance of eggs from infections in Wales under controlled conditions at 10, 12, 15, 18, 20 and 25°C. The threshold for egg viability/ development was 15°C. Mean times to hatching were 22 days at 25°C, 32 days at 20°C, extending to 66 days at 15°C. Field temperature records provided calibration of transmission schedules. Although egg production continues year-round, all eggs produced during >8 months/ year die without hatching. Output contributing significantly to transmission is restricted to 10 weeks (May-mid-July). Host infection, beginning after a time lag of 8 weeks for egg development, is also restricted to 10 weeks (July-September). Habitat temperatures (mean 15·5°C in summer 2008) allow only a narrow margin for life-cycle progress: even small temperature increases, predicted with 'global warming', enhance infection. This system provides empirical data on the metrics of transmission permitting long-term persistence of isolated parasite populations in limiting environments

Old and young bulges in late-type disk galaxies

ABRIDGED: We use HSTACS and NICMOS imaging to study the structure and colors of a sample of nine late-type spirals. We find: (1) A correlation between bulge and disks scale-lengths, and a correlation between the colors of the bulges and those of the inner disks. Our data show a trend for bulges to be more metal-enriched than their surrounding disks, but otherwise no simple age-metallicity connection between these systems; (2) A large range in bulge stellar population properties, and, in particular, in stellar ages. Specifically, in about a half of the late-type bulges in our sample the bulk of the stellar mass was produced recently. Thus, in a substantial fraction of the z=0 disk-dominated bulged galaxies, bulge formation occurs after the formation/accretion of the disk; (3) In about a half of the late-type bulges in our sample, however, the bulk of the stellar mass was produced at early epochs; (4) Even these "old" late-type bulges host a significant fraction of stellar mass in a young(er) c component; (5) A correlation for bulges between stellar age and stellar mass, in the sense that more massive late-type bulges are older than less massive late-type bulges. Since the overall galaxy luminosity (mass) also correlates with the bulge luminosity (mass), it appears that the galaxy mass regulates not only what fraction of itself ends up in the bulge component, but also "when" bulge formation takes place. We show that dynamical friction of massive clumps in gas-rich disks is a plausible disk-driven mode for the formation of "old" late-type bulges. If disk evolutionary processes are responsible for the formation of the entire family of late-type bulges, CDM simulations need to produce a similar number of initially bulgeless disks in addition to the disk galaxies that are observed to be bulgeless at z=0.Comment: ApJ in press; paper with high resolution figures available at http://www.exp-astro.phys.ethz.ch/carollo/carollo1_2006.pdf; B, I, and H surface brightness profiles published in electronic tabular for

Age Dating of a High-Redshift QSO B1422+231 at Z=3.62 and its Cosmological Implications

The observed Fe II(UV+optical)/Mg II lambda lambda 2796,2804 flux ratio from a gravitationally lensed quasar B1422+231 at z=3.62 is interpreted in terms of detailed modeling of photoionization and chemical enrichment in the broad-line region (BLR) of the host galaxy. The delayed iron enrichment by Type Ia supernovae is used as a cosmic clock. Our standard model, which matches the Fe II/Mg II ratio, requires the age of 1.5 Gyr for B1422+231 with a lower bound of 1.3 Gyr, which exceeds the expansion age of the Einstein-de Sitter Omega_0=1 universe at a redshift of 3.62 for any value of the Hubble constant in the currently accepted range, H_0=60-80 km,s^{-1},Mpc^{-1}. This problem of an age discrepancy at z=3.62 can be unraveled in a low-density Omega_0<0.2 universe, either with or without a cosmological constant, depending on the allowable redshift range of galaxy formation. However, whether the cosmological constant is a required option in modern cosmology awaits a thorough understanding of line transfer processes in the BLRs.Comment: 7 pages including 3 figures, to appear in ApJ Letter

Rainbow trout (Oncorhynchus mykiss) urea cycle and polyamine synthesis gene families show dynamic expression responses to inflammation

The research was supported by a studentship to T. Clark funded between the University of Aberdeen and BioMar Ltd.Peer reviewedPostprin

A Look At Three Different Scenarios for Bulge Formation

In this paper, we present three qualitatively different scenarios for bulge formation: a secular evolution model in which bulges form after disks and undergo several central starbursts, a primordial collapse model in which bulges and disks form simultaneously, and an early bulge formation model in which bulges form prior to disks. We normalize our models to the local z=0 observations of de Jong & van der Kruit (1994) and Peletier & Balcells (1996) and make comparisons with high redshift observations. We consider model predictions relating directly to bulge-to-disk properties. As expected, smaller bulge-to-disk ratios and bluer bulge colors are predicted by the secular evolution model at all redshifts, although uncertainties in the data are currently too large to differentiate strongly between the models.Comment: 19 pages, 6 figures, accepted for publication in the Astrophysical Journa

Stellar and Gas properties of High HI Mass-to-Light Ratio Galaxies in the Local Universe

We present a multi-wavelength study (BVRI band photometry and HI line interferometry) of nine late-type galaxies selected from the HIPASS Bright Galaxy Catalog on the basis of apparently high HI mass-to-light ratios (3 M_sun/L_sun < M_HI/L_B < 27 M_sun/L_sun). We found that most of the original estimates for M_HI/L_B based on available photographic magnitudes in the literature were too high, and conclude that genuine high HI mass-to-light ratio (>5 M_sun/L_sun) galaxies are rare in the Local Universe. Extreme high M_HI/L_B galaxies like ESO215-G?009 appear to have formed only the minimum number of stars necessary to maintain the stability of their HI disks, and could possibly be used to constrain galaxy formation models. They may to have been forming stars at a low, constant rate over their lifetimes. The best examples all have highly extended HI disks, are spatially isolated, and have normal baryonic content for their total masses but are deficent in stars. This suggests that high M_HI/L_B galaxies are not lacking the baryons to create stars, but are underluminous as they lack either the internal or external stimulation for more extensive star formation.Comment: 29 Pages, 59 Figures. Accepted for publication in AJ (to be published ~April 2006

Chemo-dynamical evolution of Globular Cluster Systems

We studied the relation between the ratio of rotational velocity to velocity dispersion and the metallicity (/\sigma_{v}-metallicity relation) of globular cluster systems (GCS) of disk galaxies by comparing the relation predicted from simple chemo-dynamical models for the formation and evolution of disk galaxies with the observed kinematical and chemical properties of their GCSs. We conclude that proto disk galaxies underwent a slow initial collapse that was followed by a rapid contraction and derive that the ratio of the initial collapse time scale to the active star formation time scale is \sim 6 for our Galaxy and \sim 15 for M31. The fundamental formation process of disk galaxies was simulated based on simple chemo-dynamical models assuming the conservation of their angular momentum. We suggest that there is a typical universal pattern in the /\sigma_{v}-metallicity relation of the GCS of disk galaxies. This picture is supported by the observed properties of GCSs in the Galaxy and in M31. This relation would deviate from the universal pattern, however, if large-scale merging events took major role in chemo-dynamical evolution of galaxies and will reflect the epoch of such merging events. We discuss the properties of the GCS of M81 and suggest the presence of past major merging event.Comment: 25 pages, 8 figures, Accepted for publication in the Astrophysical Journa