Thermal entanglement witness for materials with variable local spin lengths

We show that the thermal entanglement in a spin system using only magnetic susceptibility measurements is restricted to the insulator materials. We develop a generalization of the thermal entanglement witness that allows us to get information about the system entanglement with variable local spin lengths that can be used experimentally in conductor or insulator materials. As an application, we study thermal entanglement for the half-filled Hubbard model for linear, square and cubic clusters. We note that it is the itinerancy of electrons that favors the entanglement. Our results suggest a weak dependence between entanglement and external spin freedom degrees.Comment: 4 pages, 3 figure

Maternal sensitivity and mother-infant attachment are associated with antibiotic uptake in infancy

Attachment security has been associated with health status and symptom reporting. In this longitudinal study, we investigated the association between antibiotics uptake by infants at 9-months and mother-infant attachment at 12-months. Logistic regression analyses indicated that lower maternal sensitivity was associated with increased odds of antibiotic uptake. Furthermore, 89.7% of insecure-ambivalent infants consumed antibiotics, which contrasted with 32.5% of avoidant infants and 21.5% of secure infants. This study suggests that maternal behavior and mother-infant attachment impact on antibiotic consumption, which is worrying because antibiotics may lead to several health problems later in life and antibiotic-resistance.info:eu-repo/semantics/publishedVersio

Taquicardia de complexos QRS alargados com manifestações eletrocardiográficas atípicas elucidada através de cardio-exploração transesofágica - Relato de caso

Taquicardia de compLexos QRS aLargados (com morfoLogia de bLoqueio do ramo esquerdo) foi desencadeada durante Cardioexploração Eletrofisiológica Transesofágica. 0 E. C. G. de 12 derivações demonstrou duração dos complexos superior a 140 ms., desvio do eixo elétrico para esquerda no plano frontal e sugestivos batimentos de jusão, caracteristicas que na ausência previa de pré-excitação anter6grada ou bloqueio de ramo, sugeriram uma origem ventricular da taquiarritmia. Obteve-se reversão da mesma mediante aplicação de manobras vagais e reprodução por estimulação atrial programada. Numa etapa posterior, foi induzida taquicardia de complexos QRS estreitos, onde os impulsos iniciais apresentavam morfologia aberrante, identica ao padrao observado anteriormente. Tais achados conduziram ao diagnóstico de taquicardia supra-ventricular com condução aberrante. A observação de encurtamento do ciclo da mesma ap6s estreitamento dos complexos QRS, permitiu pressupor a presença de uma via acessória esquerda oculta envolvida na sua origem. A analise isolada de critérios eletrocardiográficos no caso em questão, poderia ter conduzido a erro diagnóstico. Uma avaliação detalhada, atraves de cardioexploração transesofagica (CETE) e manipulação autonômica possibilitou a diferenciação, assim como estabelecer 0 mecanismo preciso da taquicardia

A quadruplex qPCR for detection and differentiation of classic and natural recombinant Myxoma Virus Strains of leporids

Research Areas: Biochemistry & Molecular Biology ; ChemistryA natural recombinant myxoma virus (referred to as ha-MYXV or MYXV-Tol08/18) emerged in the Iberian hare (Lepus granatensis) and the European rabbit (Oryctolagus cuniculus) in late 2018 and mid-2020, respectively. This new virus is genetically distinct from classic myxoma virus (MYXV) strains that caused myxomatosis in rabbits until then, by acquiring an additional 2.8 Kbp insert within the m009L gene that disrupted it into ORFs m009L-a and m009L-b. To distinguish ha-MYXV from classic MYXV strains, we developed a robust qPCR multiplex technique that combines the amplification of the m000.5L/R duplicated gene, conserved in all myxoma virus strains including ha-MYXV, with the amplification of two other genes targeted by the real-time PCR systems designed during this study, specific either for classic MYXV or ha-MYXV strains. The first system targets the boundaries between ORFs m009L-a and m009L-b, only contiguous in classic strains, while the second amplifies a fragment within gene m060L, only present in recombinant MYXV strains. All amplification reactions were validated and normalized by a fourth PCR system directed to a housekeeping gene (18S rRNA) conserved in eukaryotic organisms, including hares and rabbits. The multiplex PCR (mPCR) technique described here was optimized for Taqman® and Evagreen® systems allowing the detection of as few as nine copies of viral DNA in the sample with an efficiency > 93%. This real-time multiplex is the first fast method available for the differential diagnosis between classic and recombinant MYXV strains, also allowing the detection of co-infections. The system proves to be an essential and effective tool for monitoring the geographical spread of ha-MYXV in the hare and wild rabbit populations, supporting the management of both species in the field.info:eu-repo/semantics/publishedVersio

Computer code for double beta decay QRPA based calculations

The computer code developed by our group some years ago for the evaluation of nuclear matrix elements, within the QRPA and PQRPA nuclear structure models, involved in neutrino-nucleus reactions, muon capture and β± processes, is extended to include also the nuclear double beta decay.Publicado en AIP Conference Proceedings, vol. 1625Facultad de Ciencias ExactasInstituto de Física La Plat

Standardization of blood smears prepared in transparent acetate : an alternative method for the microscopic diagnosis of malaria

Background: Due to students’ initial inexperience, slides are frequently broken and blood smears are damaged in microscopy training, leading to the need for their constant replacement. To minimize this problem a method of preparing blood smears on transparent acetate sheets was developed with the goal of implementing appropriate and more readily available teaching resources for the microscopic diagnosis of malaria. Methods: Acetate sheets derived from polyester were used to standardize the preparation and staining of thin and thick blood smears on transparent acetate sheets. Thick and thin blood smears were also prepared using the conventional method on glass slides. The staining was conducted using Giemsa staining for the thick and thin smears. Results: Microscopic examination (1,000x) of the thin and thick blood smears prepared on transparent acetate produced high-quality images for both the parasites and the blood cells. The smears showed up on a clear background and with minimal dye precipitation. It was possible to clearly identify the main morphological characteristics of Plasmodium, neutrophils and platelets. After 12 months of storage, there was no change in image quality or evidence of fungal colonization. Conclusion: Preparation of thin and thick blood smears in transparent acetate for the microscopic diagnosis of malaria does not compromise the morphological and staining characteristics of the parasites or blood cells. It is reasonable to predict the applicability of transparent acetate in relevant situations such as the training of qualified professionals for the microscopic diagnosis of malaria and the preparation of positive specimens for competency assessment (quality control) of professionals and services involved in the diagnosis of malaria