3,542 research outputs found

    A living somasteroid, Platasterias latiradiata Gray

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    16 p., 4 pl., 8 fig.http://paleo.ku.edu/contributions.htm

    Studies on the growth of Theileria infected bovine cells in immunodeficient mice

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    Coastal and Deep-Water Benthic Fishes of the Antarctic, by Hugh H. DeWitt

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    Comment on "Regularizing capacity of metabolic networks"

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    In a recent paper, Marr, Muller-Linow and Hutt [Phys. Rev. E 75, 041917 (2007)] investigate an artificial dynamic system on metabolic networks. They find a less complex time evolution of this dynamic system in real networks, compared to networks of reference models. The authors argue that this suggests that metabolic network structure is a major factor behind the stability of biochemical steady states. We reanalyze the same kind of data using a dynamic system modeling actual reaction kinetics. The conclusions about stability, from our analysis, are inconsistent with those of Marr et al. We argue that this issue calls for a more detailed type of modeling

    L1-determined ideals in group algebras of exponential Lie groups

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    A locally compact group GG is said to be ∗\ast-regular if the natural map \Psi:\Prim C^\ast(G)\to\Prim_{\ast} L^1(G) is a homeomorphism with respect to the Jacobson topologies on the primitive ideal spaces \Prim C^\ast(G) and \Prim_{\ast} L^1(G). In 1980 J. Boidol characterized the ∗\ast-regular ones among all exponential Lie groups by a purely algebraic condition. In this article we introduce the notion of L1L^1-determined ideals in order to discuss the weaker property of primitive ∗\ast-regularity. We give two sufficient criteria for closed ideals II of C∗(G)C^\ast(G) to be L1L^1-determined. Herefrom we deduce a strategy to prove that a given exponential Lie group is primitive ∗\ast-regular. The author proved in his thesis that all exponential Lie groups of dimension ≤7\le 7 have this property. So far no counter-example is known. Here we discuss the example G=B5G=B_5, the only critical one in dimension ≤5\le 5

    Linear complexity of transformed sequences

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    This paper deals with the effect of bit change errors on the linear complexity of finite sequences. Though a change in a single bit can cause a large change in linear complexity, it is shown that on the average the change will be small even when many bits, e.g. 10 % are changed. General bijections and k-fold mappings on the set of sequences of length n are studied and tight bounds are found on the average difference in linear complexity between a sequence and its image. It is also shown that any mapping, on sequences of length n that take most sequences to images of low linear complexity must take many sequences to images that are far away from them in Hamming distance

    Metabolism of gemmules from the freshwater sponge Eunapius fragilis during diapause and post-diapause states

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    Post-diapause gemmules of the freshwater sponge Eunapius fragilis remained quiescent when maintained at 5°C. Germination occurred within 48 to 72 h following warming to 20°-23°C, culminating with the emergence of a new sponge from the collagenous capsule. Both heat dissipation and oxygen consumption climbed steadily during germination and eventually reached 600% of the starting values. By comparison, energy flow was much lower over the same period of time in diapausing gemmules, clearly demonstrating metabolic depression during diapause. The calorimetric:respirometric (CR) ratio increased significantly from -354 kJ/mol O2 to -541 kJ/mol O2 between hours 3.5 and 56.5 of germination, with an average value across this period of about -495 kJ/mol O2. The low CR ratio at hour 12.5 (-374 ± 21; ± 1 SE, n = 3) was statistically below the oxycaloric equivalent, which suggests that gemmules may have experienced hypoxia during the more than 3 months of storage at 5°C prior to experiments. The increase in metabolism during germination could be blocked by perfusing the gemmules with nitrogen- saturated medium (nominally oxygen free). Developing gemmules were able to survive oxygen limitation for several hours at least; during that time energy flow was depressed to 6% of normoxic values. During germination, the range of values was 3.5 to 4.0 nmol/mg protein for ATP, 0.2 to 0.4 nmol/mg protein for ADP, and 0.5 to 0.8 nmol/mg protein for AMP. Because ATP was high even before gemmules were warmed to room temperature, it is unlikely that levels were severely compromised during the diapause condition
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