Soil isotopically exchangeable phosphorus : a comparison between E and L values

This study was designed to explain the apparent discrepancies often reported in the literature between E and L values, two parameters obtained from isotopic exchange experiments and commonly used to quantify available soil phosphate. The E and L values of the surface horizons of 10 soils from tropical, mediterranean, and temperate regions were determined. The L value was measured from a 13-wk pot experiment with common bentgrass (#Agrostis capillaris$ L.) where the available soil P was labeled with 32PO4 ions in the presence of a carrier (25-50 mg 31P/kg soil). To determine the E value, the isotopic exchange kinetic experiment was carried out on each soil. Carrier-free 32PO4 was added to the soil-solution system at a steady state and the quantity of isotopically exchangeable soil phosphate at time t, E(t), was calculated from the kinetic equation describing the decrease of radioactivity in solution with time. Results showed that L values determined after 13 wk were not significantly different from E(t) values extrapolated to the same period (t = 131 040 min). It was concluded that the L value is a particular point of the kinetic equation and isotopically exchangeable phosphate is the available P for common bentgrass. A strict equality between E(13 wk) and L values was not, however, reached for all samples. Possible causes for the differences were : an overestimation of the water-soluble phosphate due to the presence of silica and disturbance of the steady state following a too large uptake of phosphate by the crop or the application of too large quantities of carrier compared with the initial quantity of exchangeable soil phosphate. (Résumé d'auteur

Éditorial

Avec le numéro 46, Science et conservation, la revue Technè change de formule et d’éditeur. En effet, la Réunion des musées nationaux- Grand Palais ayant décidé de mettre fin en septembre 2017 à son partenariat de co-édition, le Centre de recherche et de restauration des musées de France a repris à son seul compte l’édition et la diffusion de Technè, avec le soutien fort du service des musées de France et l’investissement sans faille de Brigitte Bourgeois, rédacteur en chef, et de Marie Lionn..

Early intensification and autologous stem cell transplantation in patients with systemic AL amyloidosis: a single-centre experience

Primary systemic amyloidosis (AL amyloidosis) continues to have a very poor prognosis. Most therapeutic strategies remain unsatisfactory. Conventional chemotherapy is known to offer at best only moderate efficacy. Several studies have yielded higher complete response rates after high-dose chemotherapy and autologous stem cell transplantation (ASCT) in addition to improving outcomes in a subgroup of patients. However, the superiority of an intensive approach in AL amyloidosis has not been confirmed in a randomised trial. The precise role of ASCT remains unclear. We report our experience in 16 patients diagnosed with AL amyloidosis and treated in a multidisciplinary approach with high-dose melphalan and ASCT. Median age was 59 (39-71)years. The kidneys were predominantly affected in 75% of cases; two or more organs were affected in 38%. Median time from diagnosis to transplantation was 2 (1-4)months. Three patients (19%) developed acute renal failure and required transient dialysis. Transplant-related mortality was 6% after 100days. Haematological complete response (CR) was obtained in nine (56%) and organ response in six (38%) patients. Nine out of 12 patients (75%) with kidney involvement exhibited a sustained clinical benefit at 12months. Half of all the patients (n = 8) were alive after a median follow-up of 33months, including two in continuous CR. This suggests that high-dose chemotherapy and ASCT are still valid treatment options in AL amyloidosis and that a significant number of patients with renal involvement might benefit from this approac

Microspectroscopy reveals dust-derived apatite grains in acidic, highly-weathered Hawaiian soils

Dust deposition is an important source of phosphorus (P) to many ecosystems. However, there is little evidence of dust-derived P-containing minerals in soils. Here we studied P forms along a well-described climatic gradient on Hawaii, which is also a dust deposition gradient. Soil mineralogy and soil P forms from six sites along the climatic gradient were analyzed with bulk (X-ray diffraction and P K-edge X-ray absorption near edge structure) and microscale (X-ray fluorescence, P K-edge X-ray absorption near edge structure, and Raman) analysis methods. In the wettest soils, apatite grains ranging from 5 to 30 µm in size were co-located at the micro-scale with quartz, a known continental dust indicator suggesting recent atmospheric deposition. In addition to co-location with quartz, further evidence of dust-derived P included backward trajectory modeling indicating that dust particles could be brought to Hawaii from the major global dust-loading areas in central Asia and northern Africa. Although it is not certain whether the individual observed apatite grains were derived from long-distance transport of dust, or from local dust sources such as volcanic ash or windblown fertilizer, these observations offer direct evidence that P-containing minerals have reached surface layers of highly-weathered grassland soils through atmospheric deposition

Genome-wide association identifies nine common variants associated with fasting proinsulin levels and provides new insights into the pathophysiology of type 2 diabetes.

OBJECTIVE: Proinsulin is a precursor of mature insulin and C-peptide. Higher circulating proinsulin levels are associated with impaired β-cell function, raised glucose levels, insulin resistance, and type 2 diabetes (T2D). Studies of the insulin processing pathway could provide new insights about T2D pathophysiology. RESEARCH DESIGN AND METHODS: We have conducted a meta-analysis of genome-wide association tests of ∼2.5 million genotyped or imputed single nucleotide polymorphisms (SNPs) and fasting proinsulin levels in 10,701 nondiabetic adults of European ancestry, with follow-up of 23 loci in up to 16,378 individuals, using additive genetic models adjusted for age, sex, fasting insulin, and study-specific covariates. RESULTS: Nine SNPs at eight loci were associated with proinsulin levels (P < 5 × 10(-8)). Two loci (LARP6 and SGSM2) have not been previously related to metabolic traits, one (MADD) has been associated with fasting glucose, one (PCSK1) has been implicated in obesity, and four (TCF7L2, SLC30A8, VPS13C/C2CD4A/B, and ARAP1, formerly CENTD2) increase T2D risk. The proinsulin-raising allele of ARAP1 was associated with a lower fasting glucose (P = 1.7 × 10(-4)), improved β-cell function (P = 1.1 × 10(-5)), and lower risk of T2D (odds ratio 0.88; P = 7.8 × 10(-6)). Notably, PCSK1 encodes the protein prohormone convertase 1/3, the first enzyme in the insulin processing pathway. A genotype score composed of the nine proinsulin-raising alleles was not associated with coronary disease in two large case-control datasets. CONCLUSIONS: We have identified nine genetic variants associated with fasting proinsulin. Our findings illuminate the biology underlying glucose homeostasis and T2D development in humans and argue against a direct role of proinsulin in coronary artery disease pathogenesis

Peut-on modéliser la prise en charge des personnes âgées à l'hôpital ? (Commentaire)

Frossard Michel. Peut-on modéliser la prise en charge des personnes âgées à l'hôpital ? (Commentaire). In: Sciences sociales et santé. Volume 13, n°4, 1995. pp. 81-84