On faint companions in the close environment of star-forming dwarf galaxies. Possible external star formation triggers ?

We have searched for companion galaxies in the close environment of 98 star-forming dwarf galaxies (SFDGs) from field and low density environments, using the NASA Extragalactic Database. Most of the companions are dwarf galaxies which due to observational selection effects were previously disregarded in environmental studies of SFDGs. A subsample at low redshift, cz<2000 km/s, was chosen to partially eliminate the observational bias against distant dwarf companions. We find companion candidates for approximately 30% of the objects within a projected linear separation s_p<100 kpc and a redshift difference (Delta cz)<500 km/s. The limited completeness of the available data sets, together with the non-negligible frequency of HI clouds in the vicinity of SFDGs indicated by recent radio surveys, suggest that a considerably larger fraction of these galaxies may be accompanied by low-mass systems. This casts doubt on the hypothesis that the majority of them can be considered truly isolated. The velocity differences between companion candidates and sample SFDGs amount typically to (Delta cz)<250 km/s, and show a rising distribution towards lower (Delta cz). This is similarly found for dwarf satellites of spiral galaxies, suggesting a physical association between the companion candidates and the sample SFDGs. SFDGs with a close companion do not show significant differences in their Hbeta equivalent widths and B-V colours as compared to isolated ones. However, the available data do not allow us to rule out that interactions with close dwarf companions can influence the star formation activity in SFDGs.Comment: 9 pages, 5 figures, to appear in A&A; also available at http://www.uni-sw.gwdg.de/~knoeske/PUB_LIST/sfdg_comps.ps.g

Visual speech alters the discrimination and identification of non-intact auditory speech in children with hearing loss

OBJECTIVES: Understanding spoken language is an audiovisual event that depends critically on the ability to discriminate and identify phonemes yet we have little evidence about the role of early auditory experience and visual speech on the development of these fundamental perceptual skills. Objectives of this research were to determine 1) how visual speech influences phoneme discrimination and identification; 2) whether visual speech influences these two processes in a like manner, such that discrimination predicts identification; and 3) how the degree of hearing loss affects this relationship. Such evidence is crucial for developing effective intervention strategies to mitigate the effects of hearing loss on language development. METHODS: Participants were 58 children with early-onset sensorineural hearing loss (CHL, 53% girls, M = 9;4 yrs) and 58 children with normal hearing (CNH, 53% girls, M = 9;4 yrs). Test items were consonant-vowel (CV) syllables and nonwords with intact visual speech coupled to non-intact auditory speech (excised onsets) as, for example, an intact consonant/rhyme in the visual track (Baa or Baz) coupled to non-intact onset/rhyme in the auditory track (/–B/aa or /–B/az). The items started with an easy-to-speechread /B/ or difficult-to-speechread /G/ onset and were presented in the auditory (static face) vs. audiovisual (dynamic face) modes. We assessed discrimination for intact vs. non-intact different pairs (e.g., Baa:/–B/aa). We predicted that visual speech would cause the non-intact onset to be perceived as intact and would therefore generate more same—as opposed to different—responses in the audiovisual than auditory mode. We assessed identification by repetition of nonwords with non-intact onsets (e.g., /–B/az). We predicted that visual speech would cause the non-intact onset to be perceived as intact and would therefore generate more Baz—as opposed to az— responses in the audiovisual than auditory mode. RESULTS: Performance in the audiovisual mode showed more same responses for the intact vs. non-intact different pairs (e.g., Baa:/–B/aa) and more intact onset responses for nonword repetition (Baz for/–B/az). Thus visual speech altered both discrimination and identification in the CHL—to a large extent for the /B/ onsets but only minimally for the /G/ onsets. The CHL identified the stimuli similarly to the CNH but did not discriminate the stimuli similarly. A bias-free measure of the children’s discrimination skills (i.e., d’ analysis) revealed that the CHL had greater difficulty discriminating intact from non-intact speech in both modes. As the degree of HL worsened, the ability to discriminate the intact vs. non-intact onsets in the auditory mode worsened. Discrimination ability in CHL significantly predicted their identification of the onsets—even after variation due to the other variables was controlled. CONCLUSIONS: These results clearly established that visual speech can fill in non-intact auditory speech, and this effect, in turn, made the non-intact onsets more difficult to discriminate from intact speech and more likely to be perceived as intact. Such results 1) demonstrate the value of visual speech at multiple levels of linguistic processing and 2) support intervention programs that view visual speech as a powerful asset for developing spoken language in CHL

A spatially explicit habitat selection model incorporating home range behavior

Understanding habitat selection is of primary interest in theoretical and applied ecology. One approach is to infer habitat selection processes from differences in population densities between habitats using methods such as isodar and isoleg analysis. Another approach is to directly observe the movements of individuals. However, habitat selection models based on movement data often fail to adequately incorporate spatial processes. This is problematic if the probability of selecting a particular habitat is dependent upon its spatial context. This would occur, for example, where organisms exhibit home range behavior and the choice of habitat is dependent on its location relative to the home range. In this paper we present a spatially explicit habitat selection model for movement data that incorporates home range behavior as a spatial process. Our approach extends a previous model by formulating the probability of selecting a habitat as a function of its distance from the animal's current location and home range center. We demonstrate that these enhancements lead to more parsimonious models when applied to a koala radiotracking data set from eastern Australia. This approach could also be applied to modeling other spatial habitat selection processes, leading to more biologically meaningful models for a range of species and applications

Climate change and rising energy costs will change everything: A new mindset and action plan for 21st Century public health

Western governments currently prioritize economic growth and the pursuit of profit above alternative goals of sustainability, health and equality. Climate change and rising energy costs are challenging this consensus. The realization of the transformation required to meet these challenges has provoked denial and conflict, but could lead to a more positive response which leads to a health dividend; enhanced well-being, less overconsumption and greater equality. This paper argues that public health can make its best contribution by adopting a new mindset, discourse, methodology and set of tasks

The even darker side of the eastern gray squirrel (Sciurus carolinensis): a review of global introductions, invasion biology, and pest management strategies

Huynh, H.M., Bertolino, S., Lurz, P.W.W., Koprowski, J.L., Williams, G.R., Thompson, C.W., McAlpine, D.F

The synaptic representation of sound source location in primary auditory cortex

Akey function of the auditory system is to provide reliable information about the location of sound sources. Here, we describe how sound location is represented by synaptic input arriving onto pyramidal cells within auditory cortex by combining free-field acoustic stimulation in the frontal azimuthal plane with in vivo whole-cell recordings. We found that subthreshold activity was panoramic in that EPSPs could be evoked from all locations in all cells. Regardless of the sound location that evoked the largest EPSP, we observed a slowing in the EPSP slope along the contralateral–ipsilateral plane that was reflected in a temporal sequence of peak EPSP times. Contralateral sounds evoked EPSPs with earlier peak times and consequently generated action potential firing with shorter latencies than ipsilateral sounds. Thus, whereas spiking probability reflected the region of space evoking the largest EPSP, across the population, synaptic inputs enforced a gradient of spike latency and precision along the horizontal axis. Therefore, within auditory cortex and regardless of preferred location, the time window of synaptic integration reflects sound source location and ensures that spatial acoustic information is represented by relative timings of pyramidal cell output