Evaluation of prestress losses in prestressed concrete specimens subjected to freeze–thaw cycles

Prestressed concrete structures are considered to be reliable and durable. However, their long-term performance when subjected to frost attack is still unclear. In this work, experiments were carried out to evaluate the prestress losses in post-tensioned prestressed concrete specimens subjected to freeze–thaw cycles (FTCs). Two cases were considered: in one case, a series of specimens were prepared and tested in a freeze–thaw chamber; in the second case, the same series of specimens were tested in an indoor environment (outside the chamber). The difference between the prestress losses of the specimens inside the freeze–thaw chamber and those outside the chamber equalled the prestress losses due to FTCs. When using mathematical models to predict the prestress losses due to the FTCs, it was found that they were relatively small when the concrete was slightly damaged. However, they increased rapidly when the FTCs were repeated. The eccentricity of the prestress wires led to larger prestress losses when subjected to FTCs. Moreover, the same cross section and eccentricity resulted in similar prestress losses due to the FTCs, and the relatively high-strength concrete could withstand more FTCs.     

Edge effects of roads on temperature, light, canopy cover, and canopy height in laurel and pine forests (Tenerife, Canary Islands)

The estimation of the road edge effect is useful to understand changes induced by the road network on ecosystems. Road networks on islands may break ecosystem integrity through microclimate edge effects, which are known to be associated with disturbances to animal and plant communities. Road edge effects have been scarcely studied on oceanic islands. In this paper we studied road edge effects on microclimate and canopy structure in laurel and pine forests in Tenerife (Canary Islands). We assessed depth of road edge effect for temperature at four vertical layers (soil, litter and air at 5 cm and 1.3 m above ground), light intensity, canopy cover and height, in transects running from narrow (6–7 m width) asphalt roads and dust trails to 100 m to the interior of both forests. We used an ANOVA procedure with Helmert difference contrasts to identify the distances along transects over which edge effects were significant. We detected significant gradients for most parameters but they were consistently narrow both within and between forests. In the laurel forest, we detected highly significant gradients for soil temperature, light, and canopy cover and height in both asphalt and unpaved roads. In the pine forest, we detected a highly significant gradient for soil temperature at asphalt roads, and a significant light gradient for both asphalt and unpaved roads. From the road edge to the forest interior, significant temperature changes persisted for only 3 m, light variation persisted for 6 m, and canopy cover and height changed significantly within the first 10 m. Asphalt roads and dust trails revealed different patterns of variation for temperature between edge and interior. No differences were found between the two types of roads in edge-interior trends for light or canopy structure. The abruptness of microclimate and canopy gradients was slightly higher in the laurel forest than in the pine forest, caused by a higher edge contrast in the former. The depth of the road edge effect found in laurel and pine forests was small, but it could have cumulative effects on forest microclimate and forest associated biota at the island scale. Such changes deserve attention by local road managers for planning and design purposes.     

Understanding movement data quality

Abstract

Understanding of data quality is essential for choosing suitable analysis methods and interpreting their results. Investigation of quality of movement data, due to their spatio-temporal nature, requires consideration from multiple perspectives at different scales. We review the key properties of movement data and, on their basis, create a typology of possible data quality problems and suggest approaches to identify these types of problems.     

Paralytic shellfish poisoning detection by surface plasmon resonance-based biosensors in shellfish matrixes

The detection of paralytic shellfish poisoning (PSP) toxins in contaminated shellfish is essential for human health preservation. Ethical and technical reasons have prompted the search for new detection procedures as an alternative to the mouse bioassay. On the basis of the detection of molecular interactions by surface plasmon resonance (SPR) biosensors, an inhibition assay was developed using an anti-GTX2/3 antibody (GT13-A) and a saxitoxin-CM5 chip. This assay allowed for quantification of saxitoxin (STX), decarbamoyl saxitoxin (dcSTX), gonyautoxin 2,3 (GTX2/3), decarbamoyl gonyautoxin 2,3 (dcGTX2/3), gonyautoxin 5 (GTX5), and C 1,2 (C1/2) at concentrations from 2 to 50 ng/mL. The interference of five shellfish matrixes with the inhibition assay was analyzed. Mussels, clams, cockles, scallops, and oysters were extracted with five published methods. Ethanol extracts and acetic acid/heat extracts (AOAC Lawrence method) performed adequately in terms of surface regeneration and baseline interference, did not inhibit antibody binding to the chip surface significantly, and presented STX calibration curves similar to buffer controls in all matrixes tested. Hydrochloric acid/heat extracts (AOAC mouse bioassay method) presented surface regeneration problems, and although ethanol-acetic acid/dichloromethane extracts performed well, they were considered too laborious for routine sample testing. Overall the best results were obtained with the ethanol extraction method with calibration curves prepared in blank matrix extracts. STX recovery rate with the ethanol extraction method was 60.52+/-3.72%, with variations among species. The performance of this biosensor assay in natural samples, compared to two AOAC methods for PSP toxin quantification (mouse bioassay and HPLC), suggests that this technology can be useful as a PSP screening assay. In summary, the GT13-A-STX chip inhibition assay is capable of PSP toxin detection in ethanol shellfish extracts, with sufficient sensitivity to quantify the toxin in the range of the European regulatory limit of 80 microg/100 g of shellfish meat.     

Uncertainties in determination of 131I activity in thyroid gland

The values of the iodine (131)I uptake determined from the measurements with a NaI scintillation counter might be significantly influenced by the thyroid position in the human neck. It is shown that the ratio of the counting rate in the energy peak of 364 keV to the counting rate in the Compton scattering band can be used for the determination of the effective depth of the thyroid. The uncertainties of the standard method are discussed basing on results of calibration measurements. The investigations of 95 patients with different thyroid diseases showed that the measured iodine spectrum was considerably different from the standard for about 20% of them, indicating possible high uncertainties of the standard measurements, which assume a fixed thyroid depth of 20 mm.     

TP53 in Acute Myeloid Leukemia: Molecular Aspects and Patterns of Mutation

Mutation of the tumor suppressor gene, TP53, is associated with abysmal survival outcomes in acute myeloid leukemia (AML). Although it is the most commonly mutated gene in cancer, its occurrence is observed in only 5–10% of de novo AML, and in 30% of therapy related AML (t-AML). TP53 mutation serves as a prognostic marker of poor response to standard-of-care chemotherapy, particularly in t-AML and AML with complex cytogenetics. In light of a poor response to traditional chemotherapy and only a modest improvement in outcome with hypomethylation-based interventions, allogenic stem cell transplant is routinely recommended in these cases, albeit with a response that is often short lived. Despite being frequently mutated across the cancer spectrum, progress and enthusiasm for the development of p53 targeted therapeutic interventions is lacking and to date there is no approved drug that mitigates the effects of TP53 mutation. There is a mounting body of evidence indicating that p53 mutants differ in functionality and form from typical AML cases and subsequently display inconsistent responses to therapy at the cellular level. Understanding this pathobiological activity is imperative to the development of effective therapeutic strategies. This review aims to provide a comprehensive understanding of the effects of TP53 on the hematopoietic system, to describe its varying degree of functionality in tumor suppression, and to illustrate the need for the adoption of personalized therapeutic strategies to target distinct classes of the p53 mutation in AML management.