4,035 research outputs found

    Measuring the galaxy power spectrum with multiresolution decomposition -- II. diagonal and off-diagonal power spectra of the LCRS galaxies

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    The power spectrum estimator based on the discrete wavelet transform (DWT) for 3-dimensional samples has been studied. The DWT estimator for multi-dimensional samples provides two types of spectra with respect to diagonal and off-diagonal modes, which are very flexible to deal with configuration-related problems in the power spectrum detection. With simulation samples and mock catalogues of the Las Campanas redshift survey (LCRS), we show (1) the slice-like geometry of the LCRS doesn't affect the off-diagonal power spectrum with ``slice-like'' mode; (2) the Poisson sampling with the LCRS selection function doesn't cause more than 1-σ\sigma error in the DWT power spectrum; and (3) the powers of peculiar velocity fluctuations, which cause the redshift distortion, are approximately scale-independent. These results insure that the uncertainties of the power spectrum measurement are under control. The scatter of the DWT power spectra of the six strips of the LCRS survey is found to be rather small. It is less than 1-σ\sigma of the cosmic variance of mock samples in the wavenumber range 0.1<k<20.1 < k < 2 h Mpc−1^{-1}. To fit the detected LCRS diagonal DWT power spectrum with CDM models, we find that the best-fitting redshift distortion parameter ÎČ\beta is about the same as that obtained from the Fourier power spectrum. The velocity dispersions σv\sigma_v for SCDM and Λ\LambdaCDM models are also consistent with other σv\sigma_v detections with the LCRS. A systematic difference between the best-fitting parameters of diagonal and off-diagonal power spectra has been significantly measured. This indicates that the off-diagonal power spectra are capable of providing information about the power spectrum of galaxy velocity field.Comment: AAS LaTeX file, 41 pages, 10 figures included, accepted for publication in Ap

    Puromycin Sensitivity of Ribosomal Label after Incorporation of 14C-Labelled Amino Acids into Isolated Mitochondria from Neurospora crassa

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    Radioactive amino acids were incorporated into isolated mitochondria from Neurospora crassa. Then the mitochondrial ribosomes were isolated and submitted to density gradient centrifugation. A preferential labelling of polysomes was observed. However, when the mitochondrial suspension was treated with puromycin after amino acid incorporation, no radioactivity could be detected in either the monosomes or the polysomes. The conclusion is drawn that isolated mitochondria under these conditions do not incorporate significant amounts of amino acids into proteins of their ribosomes

    Tumour volume response, initial cell kill and cellular repopulation in B16 melanoma treated with cyclophosphamide and 1-(2-chloroethyl)-3-cyclohexyl-1-nitrosourea.

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    The relationship between tumour volume response and cell kill in B16 melanoma following treatment in vivo with cyclophosphamide (CY) and 1-(2-chloroethyl)-3-cyclohexyl-1-nitrosourea (CCNU) was investigated. Tumour volume response, expressed as growth delay, was estimated from measurements of tumour dimensions. Depression of in vitro colony-forming ability of cells from treated tumours was used as the measure of tumour cell kill. The relationship between these parameters was clearly different for the two agents studied. CY produced more growth delay (7.5 days) per decade of tumour cell kill than CCNU (2 to 3.5 days). The possibility that this was due to a technical artefact was rejected in favour of an alternative explanation that different rates of cellular repopulation in tumours treated with CY and CCNU might be responsible. Cellular repopulation was measured directly, by performing cell-survival assays at various times after treatment with doses of CY and CCNU which produced about 3 decades of cell kill. The rate of repopulation by clonogenic cells was much slower after treatment with CY than with CCNU, and this appears to account for the longer duration of the growth delay obtained with CY

    Cell yield and cell survival following chemotherapy of the B16 melanoma.

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    We describe in this paper cell survival studies, using in vitro clonogenic assays, performed on the B16 melanoma treated in situ with various cytotoxic agents. In addition we have determined the effects of these agents on the yield of cells obtained by trypsinization. In untreated tumours the mean cell yield was approximately 10(8)/g, which is 20--30% of the cells actually present in the tissue. The plating efficiency was approximately 40%. Most agents rapidly affected both cell yield and cell survival. For example, within 20--30 h, gamma-radiation and several alkylating agents reduced cell yield by about 40%. The cell yield change was associated with an increase in mean cell size. Cell yield was reduced even more (approximately 70%) by Vinca alkaloids. This large reduction was associated with extensive cell lysis, observed as an increase in the necrotic fraction of tumours from approximately 35% to approximately 70%. Adriamycin, bleomycin and Ara-C also produced a moderate reduction in cell yield (approximately 40%), but actinomycin D did not reduce cell yield and FU increased it by about 30%. Only gamma-radiation, cyclophosphamide, CCNU, BCNU and melphalan produced more than a 90% reduction in cell survival, although there was a small but measurable reduction with all other agents except vinblastine, HN2 and actinomycin D

    Clonal variation in the sensitivity of B16 melanoma to m-AMSA.

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    A hypothesis that m-AMSA may have greater cytotoxicity in melanin-containing tumour tissues, because it may reversibly bind to melanin, leading to prolonged drug exposure, was examined. Clonal lines of B16 melanoma which differed widely in pigmentation level were selected by isolating artificial lung colonies and in vitro soft-agar colonies, and implanting them into mice. Excision cell-survival assays performed 24 h after drug administration showed that in vivo sensitivity to m-AMSA progressively increased as pigmentation level decreased, but that m-AMSA drug levels measured 24 h after treatment were much lower in amelanotic than in melanotic lines. In dose-survival studies the reduced sensitivity of melanotic cell lines was revealed as a large shoulder (Dq = 27 mg/kg) though the terminal slopes for melanotic and amelanotic cell lines were similar (D10 approximately 31 mg/kg). Time-course studies indicated that there was no significant loss of drug from a melanotic cell line for 72 h after drug administration, though in an amelanotic cell line drug levels fell 10-fold in 10 h. There was, however, no evidence for prolonged drug cytotoxicity in the melanotic cell line. Using a fractionated drug-treatment regime, the greater cytotoxicity of m-AMSA to amelanotic tumour tissue was confirmed in a non-invasive regrowth-delay assay

    Influence of anaesthetics on tumour-cell kill and repopulation in B16 melanoma treated with melphalan.

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    The influence of anaesthetics on the in vivo response of B16 melanoma to melphalan was studied using an in vitro cell-survival assay. Three anaesthetics were used, Saffan (Althesin) Sagatal (Nembutal) and Hypnorm. When Saffan was administered to tumour-bearing animals before melphalan there was a significant increase in tumour-cell kill. This effect was not observed with Sagatal or Hypnorm. Maximum increase in tumour-cell kill was achieved when Saffan was administered about 1 h before melphalan, and was dependent on Saffan dose. Clonogenic tumour-cell repopulation after melphalan was rapid (TD - 1 day) and the rate was similar from 2 levels of cell kill. When Saffan was combined with melphalan the repopulation rate was the same as with melphalan alone, and the increased cell kill was reflected in increased growth delay. The in vitro response of B16 melanoma cells to melphalan was unaltered by pretreatment with, or simultaneous exposure to Saffan. The results suggest that the mechanism of the enhanced cell kill in vivo is probably due to an indirect systemic effect, rather than a direct effect on the tumour cells

    Temperature determination via STJ optical spectroscopy

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    ESA's Superconducting Tunnel Junction (STJ) optical photon-counting camera (S-Cam2) incorporates an array of pixels with intrinsic energy sensitivity. Using the spectral fitting technique common in X-ray astronomy, we fit black bodies to nine stellar spectra, ranging from cool flare stars to hot white dwarfs. The measured temperatures are consistent with literature values at the expected level of accuracy based on the predicted gain stability of the instrument. Having also demonstrated that systematic effects due to count rate are likely to be small, we then proceed to apply the temperature determination method to four cataclysmic variable (CV) binary systems. In three cases we measure the temperature of the accretion stream, while in the fourth we measure the temperature of the white dwarf. The results are discussed in the context of existing CV results. We conclude by outlining the prospects for future versions of S-Cam.Comment: 9 pages, 9 figures (11 files); uses aa.cls; accepted for publication in A&

    The Power Spectrum of Clusters of Galaxies and the Press-Schechter Approximation

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    We examine the power spectrum of clusters in the Press-Schechter (PS) theory and in N-body simulations to see how the power spectrum of clusters is related to the power spectrum of matter density fluctuations in the Universe. An analytic model for the power spectrum of clusters for their given number density is presented, both for real space and redshift space. We test this model against results from N-body simulations and find that the agreement between the analytic theory and the numerical results is good for wavelengths λ>60h−1\lambda >60h^{-1} Mpc. On smaller scales non-linear processes that are not considered in the linear PS approximation influence the result. We also use our analytic model to study the redshift-space power spectrum of clusters in cold dark matter models with a cosmological constant (Λ\LambdaCDM) and with a scale-invariant Harrison-Zel'dovich initial spectrum of density fluctuations. We find that power spectra of clusters in these models are not consistent with the observed power spectra of the APM and Abell-ACO clusters. One possible explanation for the observed power spectra of clusters is an inflationary scenario with a scalar field with the potential that has a localized steplike feature. We use the PS theory to examine the power spectrum of clusters in this model.Comment: 16 pages, 5 figures. Accepted by Ap

    Cosmic Mach Number as a Function of Overdensity and Galaxy Age

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    We carry out an extensive study of the cosmic Mach number (\mach) on scales of R=5, 10 and 20h^-1Mpc using an LCDM hydrodynamical simulation. We particularly put emphasis on the environmental dependence of \mach on overdensity, galaxy mass, and galaxy age. We start by discussing the difference in the resulting \mach according to different definitions of \mach and different methods of calculation. The simulated Mach numbers are slightly lower than the linear theory predictions even when a non-linear power spectrum was used in the calculation, reflecting the non-linear evolution in the simulation. We find that the observed \mach is higher than the simulated mean by more than 2-standard deviations, which suggests either that the Local Group is in a relatively low-density region or that the true value of \Omega_m is ~ 0.2, significantly lower than the simulated value of 0.37. We show from our simulation that the Mach number is a weakly decreasing function of overdensity. We also investigate the correlations between galaxy age, overdensity and \mach for two different samples of galaxies --- DWARFs and GIANTs. Older systems cluster in higher density regions with lower \mach, while younger ones tend to reside in lower density regions with larger \mach, as expected from the hierarchical structure formation scenario. However, for DWARFs, the correlation is weakened by the fact that some of the oldest DWARFs are left over in low-density regions during the structure formation history. For giant systems, one expects blue-selected samples to have higher \mach than red-selected ones. We briefly comment on the effect of the warm dark matter on the expected Mach number.Comment: 43 pages, including 15 figures. Accepted version in ApJ. Included correlation function of different samples of galaxies, and the cumulative number fraction distribution as a fcn. of overdensity. Reorganized figures and added some reference
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