19 research outputs found

    The Comparison of the Swift Gamma-Ray Bursts With and Without Measured Redshifts

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    Gamma-ray bursts, detected by the Swift satellite, are separated into two samples: the bursts with and without determined redshifts. These two samples are compared by the standard Student t-test and F-test. We have compared the dispersions and the mean values of the durations, peak fluxes and fluences in order to find any differences among these two samples. No essential differences were found.Comment: Published in the Proceedings of the 4th Heidelberg International Symposium on High Energy Gamma-Ray Astronomy, 200

    On the Intermediate Subgroup of the Gamma-Ray Bursts in the Swift Database

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    A sample of 286 gamma-ray bursts, detected by Swift satellite, is studied statistically by the chi^2 test and the Student t-test, respectively. The short and long subgroups are well detected in the Swift data. But no intermediate subgroup is seen. The non-detection of this subgroup in the Swift database can be explained, once it is assumed that in the BATSE database the short and the intermediate subgroups form a common subclass.Comment: Published in 4th Heidelberg International Symposium on High Energy Gamma-Ray Astronomy, 200

    A Search for Gamma-ray Burst Subgroups in the SWIFT and RHESSI Databases

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    A sample of 286 gamma-ray bursts (GRBs) detected by the Swift satellite and 358 GRBs detected by the RHESSI satellite are studied statistically. Previously published articles, based on the BATSE GRB Catalog, claimed the existence of an intermediate subgroup of GRBs with respect to duration. We use the statistical chi^2 test and the F-test to compare the number of GRB subgroups in our databases with the earlier BATSE results. Similarly to the BATSE database, the short and long subgroups are well detected in the Swift and RHESSI data. However, contrary to the BATSE data, we have not found a statistically significant intermediate subgroup in either Swift or RHESSI data.Comment: Published in Proceedings of the 2008 Nanjing Gamma-ray Burst Conferenc

    Cancer Treatment Dosing Regimens of Zoledronic Acid Result in Near-Complete Suppression of Mandible Intracortical Bone Remodeling in Beagle Dogs

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    Bisphosphonate doses used in cancer treatment are substantially higher than those used for osteoporosis. Little is known about the effects of these high doses on tissue-level remodeling suppression. The aim of this study was to assess the effects of cancer dosing regimens of zoledronic acid on tissue-level bone remodeling at different skeletal sites. Skeletally mature female beagle dogs were treated with monthly intravenous infusions of vehicle (VEH, saline) or zoledronic acid (ZOL, 0.067 mg/kg); an additional group of animals was treated daily with oral alendronate (ALN, 0.2 mg/kg/day). Doses of ZOL and ALN were, on a milligram per kilogram basis, consistent with those used for cancer and osteoporosis, respectively. Following either 3 or 6 months of treatment, animals were euthanized, and mandible, rib, and tibia were processed for dynamic bone histology. There was no evidence of oral lesions or bone matrix necrosis in the mandibles of any animals. After 3 months, the rate of intracortical bone remodeling in the mandible was significantly suppressed with ZOL (−95%) compared with VEH; by 6 months, ZOL had produced nearly complete suppression (−99%) compared with VEH. ZOL also significantly suppressed remodeling in the rib cortex at both 3 (−83%) and 6 (−85%) months compared with VEH; tibia cortex bone formation rate was nonsignificantly lower with ZOL treatment (−68% to −75%). Remodeling suppression in ZOL-treated animals was significantly greater than in ALN-treated animals at both the mandible and the rib; ALN and VEH were not different for any of the assessed parameters at any of the sites. Compared across skeletal sites, the absolute level of remodeling suppression with ZOL treatment was significantly greater at sites with higher remodeling, whereas the percent reduction was similar among the sites. These results document nearly complete intracortical remodeling suppression resulting from monthly intravenous zoledronic acid dosing, with changes being most dramatic at the mandible. Copyright © 2010 American Society for Bone and Mineral Researc

    Non Destructive Characterization of Cortical Bone MicroDamage by Nonlinear Resonant Ultrasound Spectroscopy

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    The objective of the study was to evaluate the ability of a nonlinear ultrasound technique, the so-called nonlinear resonant ultrasound spectroscopy (NRUS) technique, for detecting early microdamage accumulation in cortical bone induced by four-point bending fatigue. Small parallelepiped beam-shaped human cortical bone specimens were subjected to cyclic four-point bending fatigue in several steps. The specimens were prepared to control damage localization during four-point bending fatigue cycling and to unambiguously identify resonant modes for NRUS measurements. NRUS measurements were achieved to follow the evolution of the nonlinear hysteretic elastic behavior during fatigue-induced damage. After each fatigue step, a small number of specimens was removed from the protocol and set apart to quantitatively assess the microcrack number density and length using synchrotron radiation micro-computed tomography (SR-”CT). The results showed a significant effect of damage steps on the nonlinear hysteretic elastic behavior. No significant change in the overall length of microcracks was observed in damaged regions compared to the load-free control regions. Only an increased number of shortest microcracks, those in the lowest quartile, was noticed. This was suggestive of newly formed microcracks during the early phases of damage accumulation. The variation of nonlinear hysteretic elastic behavior was significantly correlated to the variation of the density of short microcracks. Our results suggest that the nonlinear hysteretic elastic behavior is sensitive to early bone microdamage. Therefore NRUS technique can be used to monitor fatigue microdamage progression in in vitro experiments.BONUS_07BLAN019
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