20,523 research outputs found

    Quantitative estimates of fish abundance from boat electrofishing

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    Multiple removals by boat electro-fishing were used to estimate fish populations in non-wadeable habitats in New Zealand lakes and rivers. Mean capture probability was 0.47±h0.10 (± 95% CI) from 35 population estimates made with 2-7 successive removals. The relationship between the population estimate from the Zippin method (Y)and the number of fish caught in the first removal (X) was significant (adjusted r2=0.84, P<0.001; Figure 2). The least-squares regression was Y = 1.55X 1.23. Mean density ± 95% confidence interval for 13 fishing occasions was 30±27 fish 100 m- 2. Mean biomass of fish for sites was 78±39 g m-2 (range 29 to 245 g m-2). Koi carp comprised the largest proportion of the fish biomass wherever they were present. The high biomasses of koi carp estimated in these results (mean 56±33 g m-2) suggest that they can reach problematic abundances in New Zealand. Bioniass of spawning koi carp can exceed 400 g m-2

    Radial Trends in IMF-Sensitive Absorption Features in Two Early-Type Galaxies: Evidence for Abundance-Driven Gradients

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    Samples of early-type galaxies show a correlation between stellar velocity dispersion and the stellar initial mass function (IMF) as inferred from gravity-sensitive absorption lines in the galaxies' central regions. To search for spatial variations in the IMF, we have observed two early-type galaxies with Keck/LRIS and measured radial gradients in the strengths of absorption features from 4000-5500 \AA \, and 8000-10,000 \AA. We present spatially resolved measurements of the dwarf-sensitive spectral indices NaI (8190 \AA) and Wing-Ford FeH (9915 \AA), as well as indices for species of H, C2_2, CN, Mg, Ca, TiO, and Fe. Our measurements show a metallicity gradient in both objects, and Mg/Fe consistent with a shallow gradient in \alpha-enhancement, matching widely observed trends for massive early-type galaxies. The NaI index and the CN1_1 index at 4160 \AA \, exhibit significantly steeper gradients, with a break at r0.1reffr \sim 0.1 r_{\rm eff} (r300r \sim 300 pc). Inside this radius NaI strength increases sharply toward the galaxy center, consistent with a rapid central rise in [Na/Fe]. In contrast, the ratio of FeH to Fe index strength decreases toward the galaxy center. This behavior cannot be reproduced by a steepening IMF inside 0.1reff0.1 r_{\rm eff} if the IMF is a single power law. While gradients in the mass function above 0.4M\sim 0.4 M_\odot may occur, exceptional care is required to disentangle these IMF variations from the extreme variations in individual element abundances near the galaxies' centers.Comment: Accepted for publication in ApJ. Updates from v1 include an expanded comparison of measured index strengths to SPS models. 20 page body + 7 page appendix + references. Includes 25 figure

    The Stellar Activity - Rotation Relationship

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    Using a new catalog of 824 solar and late-type stars with X-ray luminosities and rotation periods we have studied the relationship between rotation and stellar activity. From an unbiased subset of this sample the power law slope of the unsaturated regime, LX/LbolRoβL_X/L_{bol}\propto Ro^\beta, is fit as β=2.70±0.13\beta=-2.70\pm0.13. This is inconsistent with the canonical β=2\beta=-2 slope to a confidence of 5σ\sigma and argues for an interface-type dynamo. Super-saturation is observed for the fastest rotators in our sample and its parametric dependencies are explored. Significant correlations are found with both the corotation radius and the excess polar updraft, the latter theory being supported by other observations. We also present a new X-ray population synthesis model of the mature stellar component of our Galaxy and use it to reproduce deep observations of a high Galactic latitude field. The model, XStar, can be used to test models of stellar spin-down and dynamo decay, as well as for estimating stellar X-ray contamination rates for non-stellar studies.Comment: 4 pages, 4 figures. To appear in the proceedings of Cool Stars 17: 17th Cambridge Workshop on Cool Stars, Stellar Systems, and the Sun, AN 334, 1-2, Eds Klaus Strassmeier and Mercedes Lopez-Morale

    Active Travel Co-Benefits of Travel Demand Management Policies that Reduce Greenhouse Gas Emissions, MTI Report 12-12

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    There is increasing evidence that improved health outcomes may be significant co-benefits of land use plans and transport policies that increase active transport (or walking and biking for purposeful travel) and reduce greenhouse gas emissions (GHGs) from vehicle miles traveled (VMT). A greater understanding of these benefits may broaden the constituency for regional planning that supports local and national GHG reduction goals. In this study, California’s activity-based travel demand model (ABM) is applied to (1) demonstrate how this new generation of travel models can be used to produce the active travel data (age and sex distributions) required by comparative risk assessment models to estimate health outcomes for alternative land use and transport plans and to (2) identify the magnitude of change in active travel that may be possible from land use, transit, and vehicle pricing policies for California and its five major regions for a future 2035 time horizon. The results of this study suggest that distance-based vehicle pricing may increase walking by about 10% and biking by about 17%, and concurrently GHG from VMT may be reduced by about 16%. Transit expansion and supportive development patterns may increase active travel by about 2% to 3% for both walk and bike modes while also reducing VMT by about 4% on average. The combination of all three policies may increase time spent walking by about 13% and biking by about 19%, and reduce VMT by about 19%

    Source-Channel Diversity for Parallel Channels

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    We consider transmitting a source across a pair of independent, non-ergodic channels with random states (e.g., slow fading channels) so as to minimize the average distortion. The general problem is unsolved. Hence, we focus on comparing two commonly used source and channel encoding systems which correspond to exploiting diversity either at the physical layer through parallel channel coding or at the application layer through multiple description source coding. For on-off channel models, source coding diversity offers better performance. For channels with a continuous range of reception quality, we show the reverse is true. Specifically, we introduce a new figure of merit called the distortion exponent which measures how fast the average distortion decays with SNR. For continuous-state models such as additive white Gaussian noise channels with multiplicative Rayleigh fading, optimal channel coding diversity at the physical layer is more efficient than source coding diversity at the application layer in that the former achieves a better distortion exponent. Finally, we consider a third decoding architecture: multiple description encoding with a joint source-channel decoding. We show that this architecture achieves the same distortion exponent as systems with optimal channel coding diversity for continuous-state channels, and maintains the the advantages of multiple description systems for on-off channels. Thus, the multiple description system with joint decoding achieves the best performance, from among the three architectures considered, on both continuous-state and on-off channels.Comment: 48 pages, 14 figure

    Age composition, growth, and reproduction of koi carp (Cyprinus carpio L.) in the lower Waikato, New Zealand

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    A total of 566 koi carp (Cyprinus carpio) from the lower Waikato region were aged from scales and opercular bones, and growth was modelled with the von Bertalanffy growth function. There was no difference in growth rate between male and female carp. Growth of koi carp between zero and 3 years of age was lower than that of common carp in Europe and Australia. However, after 5 years of age the growth of koi carp was higher than that of common carp in Europe, but still below that of carp in Australia. Males rarely lived in excess of 8 years, whereas females lived to 12 years. Mean total fecundity calculated from 44 running-ripe females was 299 000 oocytes (±195 600 SD) (range 29 800–771 000). Relative fecundity ranged from 19 300 to 216 000 oocytes kg–1 total body weight, with a mean of 97 200 (±35 000 SD) oocytes kg–1. Feral koi carp in the Waikato are capable of multiple spawnings within their lifetimes. Within a spawning season, Waikato populations of feral koi carp contained females that spawned once, and females that had the potential to have spawned repeatedly. Female gonadosomatic index (GSI) varied with season and was negatively related to water temperature

    2-aminophenols containing electron-withdrawing groups from N-aryl hydroxylamines

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    Reaction of substituted N-aryl hydroxylamines with methanesulfonyl chloride, p-toluenesulfonyl chloride, or trifluoromethanesulfonic anhydride under basic conditions leads to the rearranged 2-aminophenols (45-94%). The overall reaction sequence can be performed using polymer-supported sulfonyl chloride resin allowing for the effective conversion of N-aryl hydroxylamines to the 2-aminophenols without the need for chromatography

    Costs of colour change in fish: food intake and behavioural decisions

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    Many animals, particularly reptiles, amphibians, fish and cephalopods, have the ability to change their body colour, for functions including thermoregulation, signalling and predator avoidance. Many fish plastically darken their body colouration in response to dark visual backgrounds, and this functions to reduce predation risk. Here, we tested the hypotheses that colour change in fish (1) carries with it an energetic cost and (2) affects subsequent shoal and habitat choice decisions. We demonstrate that guppies (Poecilia reticulata) change colour in response to dark and light visual backgrounds, and that doing so carries an energetic cost in terms of food consumption. By increasing food intake, however, guppies are able to maintain growth rates and meet the energetic costs of changing colour. Following colour change, fish preferentially choose habitats and shoals that match their own body colouration, and maximise crypsis, thus avoiding the need for further colour change but also potentially paying an opportunity cost associated with restriction to particular habitats and social associates. Thus, colour change to match the background is complemented by behavioural strategies, which should act to maximise fitness in variable environments. © 2013. Published by The Company of Biologists Ltd
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