Observations of a diapycnal shortcut to adiabatic upwelling of Antarctic Circumpolar Deep Water

In the Southern Ocean, small-scale turbulence causes diapycnal mixing which influences important water mass transformations, in turn impacting large-scale ocean transports such as the Meridional Overturning Circulation (MOC), a key controller of Earth's climate. We present direct observations of mixing over the Antarctic continental slope between water masses that are part of the Southern Ocean MOC. A 12 h time series of microstructure turbulence measurements, hydrography, and velocity observations off Elephant Island, north of the Antarctic Peninsula, reveals two concurrent bursts of elevated dissipation of O(10�6)�W�kg�1, resulting in heat fluxes �10 times higher than basin-integrated Drake Passage estimates. This occurs across the boundary between adjacent adiabatic upwelling and downwelling overturning cells. Ray tracing to nearby topography shows mixing between 300 and 400 m is consistent with the breaking of locally generated internal tidal waves. Since similar conditions extend to much of the Antarctic continental slope where these water masses outcrop, diapycnal mixing may contribute significantly to upwelling

Clinical classification and long‐term outcomes of seronegative coeliac disease: a 20‐year multicentre follow‐up study

Background Seronegative coeliac disease is poorly defined. Aims To study clinical phenotypes and long-term outcomes of seronegative coeliac disease in a multicentre cohort over 20 years. Methods Seronegative coeliac disease was diagnosed in HLA-DQ2/DQ8-positive patients with villous atrophy (VA), negative IgA endomysial (EmA), tissue transglutaminase (tTG) and deamidated-gliadin antibodies (DGP), clinical and histological response to a gluten-free diet (GFD), and no alternative causes for VA. In patients with IgA deficiency, coeliac disease was diagnosed through VA, positive IgG EmA/tTG/DGP and clinical/histological response to a GFD (coeliac disease+IgAd). Patients with seropositive coeliac disease served as controls. Results Of 227 patients previously diagnosed with seronegative coeliac disease, true seronegative coeliac disease was confirmed in 84, coeliac disease+IgAd in 48, and excluded in 55. Lack of follow-up duodenal biopsy precluded diagnosing seronegative coeliac disease in 40 patients. 2084 patients with seropositive coeliac disease served as controls. True seronegative coeliac disease had more severe symptoms at diagnosis and a higher risk of complications (HR 10.87, 95% CI 6.11-19.33, P < 0.001) and mortality (HR 2.18, 95% CI 1.12-4.26, P < 0.01) than seropositive coeliac disease. There were no differences between true seronegative coeliac disease and coeliac disease+IgAd. On multivariate analysis, age at diagnosis, lack of clinical response to a GFD, true seronegative coeliac disease, coeliac disease+IgAd, and classical presentation predicted complications. Age at diagnosis, complications and absence of clinical response to a GFD predicted mortality. Conclusions Seronegative coeliac disease has a more aggressive disease phenotype than seropositive coeliac disease. These data argue against over-reliance on serology for the diagnosis of coeliac disease and support a strict clinical and histologic follow-up in seronegative coeliac disease

Preparação e caracterização de colágeno aniônico por hidrólise seletiva de grupos carboxamida internos Preparation and characterization of anionic collagen by selective hydrolysis of internal carboxamide groups

Este trabalho descreve um processo para hidrólise seletiva de grupos carboxamidas de resíduos de asparagina e glutamina presentes em matrizes colagênicas, para a obtenção de colágeno aniônico para produção de novos biomateriais. Os resultados mostraram que em meio alcalino e na presença de metais alcalinos e alcalinos terrosos, os grupos carboxamidas da proteína são seletivamente hidrolizados para dar origem a pH neutro, a materiais de colágeno com um aumento de 106 de carga negativas, em relação à matrizes não modificadas. Embora não tenham sido observadas alterações na estrutura secundária da proteína ou na organização microfibrilar da matriz, modificações significativas foram observadas no padrão da sub-periodicidade do período D da estrutura microfibrilar, que provavelmente são devidas a um aumento da intensidade de interações eletrostáticas.<br>This work describes a process for the selective hydrolysis of carboxamide groups of asparagine and glutamine found in collagen polymeric matrices for the preparation of new charged collagen biomaterials. The results showed that under alkaline conditions and in the presence of alkaline and alkaline earth metals, protein carboxamide side chain groups were selectively hydrolyzed to produce collagen matrices with net increase of 106 negative charges at neutral pH, in comparison to native matrices. Although no changes were observed at the secondary protein structure or at the microfibrillar level of collagen matrix organization, significative changes were detected in the pattern of the sub-periodicity of the D-period, probably due to an increase in electrostatic interaction