32 research outputs found

    Non-linear general relativistic effects in the observed redshift

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    We present the second-order expression for the observed redshift, accounting for all the relativistic effects from the light propagation and from the frame change at the observer and the source positions. We derive the generic gauge-transformation law that any observable quantities should satisfy, and we verify our second-order expression for the observed redshift by explicitly checking its gauge transformation property. This is the first time an explicit verification is made for the second-order calculations of observable quantities. We present our results in popular gauge choices for easy use and discuss the origin of disagreements in previous calculations.Comment: 44 pages, 1 figure, Version published in JCA

    Galaxy Two-Point Correlation Function in General Relativity

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    We perform theoretical and numerical studies of the full relativistic two-point galaxy correlation function, considering the linear-order scalar and tensor perturbation contributions and the wide-angle effects. Using the gauge-invariant relativistic description of galaxy clustering and accounting for the contributions at the observer position, we demonstrate that the complete theoretical expression is devoid of any long-mode contributions from scalar or tensor perturbations and it lacks the infrared divergences in agreement with the equivalence principle. By showing that the gravitational potential contribution to the correlation function converges in the infrared, our study justifies an IR cut-off (kIR≤H0)(k_{\text{IR}} \leq H_0) in computing the gravitational potential contribution. Using the full gauge-invariant expression, we numerically compute the galaxy two-point correlation function and study the individual contributions in the conformal Newtonian gauge. We find that the terms at the observer position such as the coordinate lapses and the observer velocity (missing in the standard formalism) dominate over the other relativistic contributions in the conformal Newtonian gauge such as the source velocity, the gravitational potential, the integrated Sachs-Wolf effect, the Shapiro time-delay and the lensing convergence. Compared to the standard Newtonian theoretical predictions that consider only the density fluctuation and redshift-space distortions, the relativistic effects in galaxy clustering result in a few percent-level systematic errors beyond the scale of the baryonic acoustic oscillation. Our theoretical and numerical study provides a comprehensive understanding of the relativistic effects in the galaxy two-point correlation function, as it proves the validity of the theoretical prediction and accounts for effects that are often neglected in its numerical evaluation.Comment: 35 pages, 9 figures, submitted to JCA

    Galaxy Power Spectrum in General Relativity

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    We present the galaxy power spectrum in general relativity. Using a novel approach, we derive the galaxy power spectrum taking into account all the relativistic effects in observations. In particular, we show independently of survey geometry that relativistic effects yield no divergent terms (proportional to k−4Pm(k)k^{-4}P_m(k) or k−2Pm(k)k^{-2}P_m(k) on all scales) that would mimic the signal of primordial non-Gaussianity. This cancellation of such divergent terms is indeed expected from the equivalence principle, meaning that any perturbation acting as a uniform gravity on the scale of the experiment cannot be measured. We find that the unphysical infrared divergence obtained in previous calculations occurred only due to not considering all general relativistic contributions consistently. Despite the absence of divergent terms, general relativistic effects represented by non-divergent terms alter the galaxy power spectrum at large scales (smaller than the horizon scale). In our numerical computation of the full galaxy power spectrum, we show the deviations from the standard redshift-space power spectrum due to these non-divergent corrections. We conclude that, as relativistic effects significantly alter the galaxy power spectrum at k≲keqk\lesssim k_{eq}, they need to be taken into account in the analysis of large-scale data.Comment: 29 pages, 10 figures, accepted for publication in JCA

    Human Genotoxic Study Carried Out Two Years after Oil Exposure during the Clean-up Activities Using Two Different Biomarkers

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    Micronuclei, comet and chromosome alterations assays are the most widely used biomarkers for determining the genotoxic damage in a population exposed to genotoxic chemicals. While chromosome alterations are an excellent biomarker to detect short- and long-term genotoxic effects, the comet assay only measures early biological effects, and furthermore it is unknown whether nuclear abnormalies, such as those measured in the micronucleus test, remain detectable long-term after an acute exposure. In our previous study, an increase in structural chromosome alterations in fishermen involved in the clean-up of the Prestige oil spill, two years after acute exposure, was detected. The aim of this study is to investigate whether, in lymphocytes from peripheral blood, the nuclear abnormalies (micronucleus, nucleoplasmic bridges and nuclear buds) have a similar sensitivity to the chromosome damage analysis for genotoxic detection two years after oil exposure in the same non-smoker individuals and in the same peripheral blood extraction. No significant differences in nuclear abnormalies frequencies between exposed and non-exposed individuals were found (p > 0.05). However, chromosome damage, in the same individuals, was higher in exposed vs. non-exposed individuals, especially for chromosome lesions (p < 0.05). These findings, despite the small sample size, suggest that nuclear abnormalities are probably less-successful biomarkers than are chromosome alterations to evaluate genotoxic effects two or more years after an exposure to oil. Due to the great advantage of micronucleus automatic determination, which allows for a rapid study of hundreds of individuals exposed to genotoxic chemical exposure, further studies are needed to confirm whether this assay is or is not useful in long-term genotoxic studies after the toxic agent is no longer present

    Human genotoxic study carried out two years after oil exposure during the clean-up activities using two different biomarkers

    Get PDF
    Micronuclei, comet and chromosome alterations assays are the most widely used biomarkers for determining the genotoxic damage in a population exposed to genotoxic chemicals. While chromosome alterations are an excellent biomarker to detect short- and long-term genotoxic effects, the comet assay only measures early biological effects, and furthermore it is unknown whether nuclear abnormalies, such as those measured in the micronucleus test, remain detectable long-term after an acute exposure. In our previous study, an increase in structural chromosome alterations in fishermen involved in the clean-up of the Prestige oil spill, two years after acute exposure, was detected. The aim of this study is to investigate whether, in lymphocytes from peripheral blood, the nuclear abnormalies (micronucleus, nucleoplasmic bridges and nuclear buds) have a similar sensitivity to the chromosome damage analysis for genotoxic detection two years after oil exposure in the same non-smoker individuals and in the same peripheral blood extraction. No significant differences in nuclear abnormalies frequencies between exposed and non-exposed individuals were found (p > 0.05). However, chromosome damage, in the same individuals, was higher in exposed vs. non-exposed individuals, especially for chromosome lesions (p < 0.05). These findings, despite the small sample size, suggest that nuclear abnormalities are probably less-successful biomarkers than are chromosome alterations to evaluate genotoxic effects two or more years after an exposure to oil. Due to the great advantage of micronucleus automatic determination, which allows for a rapid study of hundreds of individuals exposed to genotoxic chemical exposure, further studies are needed to confirm whether this assay is or is not useful in long-term genotoxic studies after the toxic agent is no longer present
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