Validation of computational liquefaction for tailings: Tar Island slump

Finite-element analyses using critical state theory proved necessary to understand the development of static liquefaction during three recent large tailing dam failures at Fundao (in Brazil), Cadia (in Australia) and Brumadinho (in Brazil). However, the complexity of these events prevents these analyses being viewed as a complete validation of the methodology. Here the authors evaluate a far simpler case of static liquefaction: The 1974 Tar Island slump (in Canada). This upstream slump involved a rapid drop of 5 m during construction of a 12.5 m high upstream raise over loose tailings. While not a dam stability issue, the event has the attraction for validation of being load-induced, with simple geometry, and with known material properties and in situ state. The computed liquefaction develops from a prior drained condition before propagating rapidly undrained-there are similarities to the video record at Brumadinho (an animation is provided as online supplementary material to illustrate this). A range of scenarios are explored, with the base case of taking reported conditions at face value giving deformations close to those measured. An important aspect was using elastic shear moduli determined by geophysical methods. The analyses were carried out with commercial software (Plaxis) and used critical state theory with largely familiar soil properties measured by standard methods

Impact of Normothermic Preservation with Extracellular Type Solution Containing Trehalose on Rat Kidney Grafting from a Cardiac Death Donor

BACKGROUND: The aim of this study was to investigate factors that may improve the condition of a marginal kidney preserved with a normothermic solution following cardiac death (CD) in a model of rat kidney transplantation (RTx). METHODS: Post-euthanasia, Lewis (LEW) donor rats were left for 1 h in a 23°C room. These critical kidney grafts were preserved in University of Wisconsin (UW), lactate Ringer's (LR), or extracellular-trehalose-Kyoto (ETK) solution, followed by intracellular-trehalose-Kyoto (ITK) solution at 4, 23, or 37°C for another 1 h, and finally transplanted into bilaterally nephrectomized LEW recipient rats (n = 4-6). Grafts of rats surviving to day 14 after RTx were evaluated by histopathological examination. The energy activity of these marginal rat kidneys was measured by high-performance liquid chromatography (HPLC; n = 4 per group) and fluorescence intensity assay (n = 6 per group) after preservation with UW or ETK solutions at each temperature. Finally, the transplanted kidney was assessed by an in vivo luciferase imaging system (n = 2). RESULTS: Using the 1-h normothermic preservation of post-CD kidneys, five out of six recipients in the ETK group survived until 14 days, in contrast to zero out of six in the UW group (p<0.01). Preservation with ITK rather than ETK at 23°C tended to have an inferior effect on recipient survival (p = 0.12). Energy activities of the fresh donor kidneys decreased in a temperature-dependent manner, while those of post-CD kidneys remained at the lower level. ETK was superior to UW in protecting against edema of the post-CD kidneys at the higher temperature. Luminescence intensity of successful grafts recovered within 1 h, while the intensity of grafts of deceased recipients did not change at 1 h post-reperfusion. CONCLUSIONS: Normothermic storage with extracellular-type solution containing trehalose might prevent reperfusion injury due to temperature-dependent tissue edema

Am J Prev Med

CC999999/Intramural CDC HHS/United States2017-02-19T00:00:00Z26456878PMC531651

History of clinical transplantation

How transplantation came to be a clinical discipline can be pieced together by perusing two volumes of reminiscences collected by Paul I. Terasaki in 1991-1992 from many of the persons who were directly involved. One volume was devoted to the discovery of the major histocompatibility complex (MHC), with particular reference to the human leukocyte antigens (HLAs) that are widely used today for tissue matching.1 The other focused on milestones in the development of clinical transplantation.2 All the contributions described in both volumes can be traced back in one way or other to the demonstration in the mid-1940s by Peter Brian Medawar that the rejection of allografts is an immunological phenomenon.3,4 © 2008 Springer New York

History of clinical transplantation

The emergence of transplantation has seen the development of increasingly potent immunosuppressive agents, progressively better methods of tissue and organ preservation, refinements in histocompatibility matching, and numerous innovations is surgical techniques. Such efforts in combination ultimately made it possible to successfully engraft all of the organs and bone marrow cells in humans. At a more fundamental level, however, the transplantation enterprise hinged on two seminal turning points. The first was the recognition by Billingham, Brent, and Medawar in 1953 that it was possible to induce chimerism-associated neonatal tolerance deliberately. This discovery escalated over the next 15 years to the first successful bone marrow transplantations in humans in 1968. The second turning point was the demonstration during the early 1960s that canine and human organ allografts could self-induce tolerance with the aid of immunosuppression. By the end of 1962, however, it had been incorrectly concluded that turning points one and two involved different immune mechanisms. The error was not corrected until well into the 1990s. In this historical account, the vast literature that sprang up during the intervening 30 years has been summarized. Although admirably documenting empiric progress in clinical transplantation, its failure to explain organ allograft acceptance predestined organ recipients to lifetime immunosuppression and precluded fundamental changes in the treatment policies. After it was discovered in 1992 that long-surviving organ transplant recipient had persistent microchimerism, it was possible to see the mechanistic commonality of organ and bone marrow transplantation. A clarifying central principle of immunology could then be synthesized with which to guide efforts to induce tolerance systematically to human tissues and perhaps ultimately to xenografts

Multilevel approach for brick masonry walls - Part II: On the use of equivalent continua

This work investigates the possibility of using equivalent continua within a multilevel strategy for the analysis of brick masonry walls, as prototypes for the in-plane behavior of masonry buildings. This strategy, proposed and discussed in detail in Part I of the same paper, lies in an iterative solution scheme which uses two levels, local and global, of description: the former accounts for the interaction between the single bricks; the latter, modeled as a coarse Finite Element discretization, accounts for global interactions. Within the same Finite Element format and strategy, the paper compares the performances of schemes implementing the identification procedures based on equivalent continua with those implementing the algebraic re-parametrization of the local model proposed in Part I. The former, while suitable for a synthetic representation of masonry behavior, does not prove to be convenient for a multilevel solution strategy