106 research outputs found

    Cydia pomonella, the first eradicated pest in Brazil.

    Get PDF
    Cydia pomonella is the most important apple and pear pest in the main producing areas of the world. In Brazil, C. pomonella was detected for the first time in 1991, and the specimen captured was identified by Dr. Vitor Becker. With the detection of this specimen in the urban area of Vacaria ? RS, Brazil, the monitoring was intensified in all the Brazilian temperate fruit producing region. The monitoring included urban and commercial areas in the producing region, as well as urban areas in the route of apple transport from Argentina and Chile into Brazil. Traps were also installed in the CEASAS of the Southern Region in Brazil. The first year of full monitoring was in the 1997/98 season, when around 22,500 males were captured in the urban areas of Bom Jesus, Caxias do Sul, and Vacaria, in the state of Rio Grande do Sul, and in Lages (Santa Catarina). Considering the severity of the infestation, a National Committee was created, composed of representatives from governmental agencies and grower associations, defining the population suppression program through the installation of panels with insecticide and sexual pheromones (i.e. attract-and-kill system). Due to the costs and delay in the registration of the attract-and-kill system, the suppression program was suspended. In July of 2002, the Committee decided for the eradication of the host plants in the infested urban areas, with the removal directed to the points of greater population density. During the eradication program, around 95,000 host plants were removed and replaced with non-host plants. With the removal of hosts, there was a decline in the captures, culminating with the capture of the last C. pomonella in Brazil in November of 2011. Based on the results of the program, on 5 May 2014, the Ministry of Agriculture, Livestock and Food Supply officially declared the eradication of C. pomonella in Brazil. This was registered through the Normative Instruction no. 10

    Rapid preparation of rodent testicular cell suspensions and spermatogenic stages purification by flow cytometry using a novel blue-laser-excitable vital dye

    Get PDF
    Availability of purified or highly enriched fractions representing the various spermatogenic stages is a usual requirement to study mammalian spermatogenesis at the molecular level. Fast preparation of high quality testicular cell suspensions is crucial when flow cytometry (FCM) is chosen to accomplish the stage/s purification. Formerly, we reported a method to rapidly obtain good quality rodent testicular cell suspensions for FCM analysis and sorting. Using that method we could distinguish and purify early meiocytes (leptotene/zygotene stages, L/Z) from more advanced ones (pachytene, P) in guinea pig, which presents an unusually high content of early stages. Here we present an upgrade of that method with improvements that have enabled the obtainment of high-purity meiotic substages also from mouse testis, namely: • Shortening of the mechanical disaggregation time and elimination of a 25µm-filtration step, to optimize the integrity of the suspension and ensure the presence of large P cells. • Inclusion of a non-cytotoxic, DNA-specific, 488_nm-excitable vital fluorochrome (Vybrant-DyeCycle-Green [VDG], Invitrogen) instead of Hoechst 33342 (requires UV laser, which can damage nucleic acids) or propidium iodide (usually related to dead/damaged cells). As far as we know, this is the first report on the use of this fluorochrome on testicular cells.Agencia Nacional de Investigación e Innovació

    Potencial de resposta à adubação para N, P, K, Ca e Mg em cupuaçueiros avaliados por diferentes normas DRIS .

    Get PDF
    O potencial de resposta à adubação é uma ferramenta utilizada para a interpretação dos valores dos índices DRIS, de forma que pode ser útil para verificar se diferentes grupos de normas resultam em diagnósticos distintos ou semelhantes entre si. Neste sentido, objetivou-se avaliar o comportamento do diagnóstico nutricional, submetidos a cinco grupos de normas DRIS. Para isto, amostras foliares de cupuaçueiros foram coletadas de pomares comerciais, cuja idade das plantas variou de 5 a 18 anos, sob monocultivo e sistemas agroflorestais (SAF?s), obtendo-se para cada relação nutricional entre os nutrientes N, P, K, Ca, Mg, as normas DRIS bivariadas, as quais foram obtidas para o conjunto das populações monitoradas e para subpopulações específicas. As diferentes normas DRIS resultaram em diagnósticos semelhantes para N, P e Ca, enquanto que para K e Mg os diagnósticos produzidos distinguiram-se entre as normas resultando em desvios nutricionais

    Protótipos de equipamentos para produção de hortaliças.

    Get PDF
    bitstream/item/142209/1/Prototpios-equipamentos.pd

    Poly(ADP-ribosylation) is present in murine sciatic nerve fibers and is altered in a Charcot-Marie-Tooth-1E neurodegenerative model

    Get PDF
    Background. Poly-ADP-ribose (PAR) is a polymer synthesized by poly-ADP-ribose polymerases (PARPs) as a postranslational protein modification and catabolized mainly by poly-ADP-ribose glycohydrolase (PARG). In spite of the existence of cytoplasmic PARPs and PARG, research has been focused on nuclear PARPs and PAR, demonstrating roles in the maintenance of chromatin architecture and the participation in DNA damage responses and transcriptional regulation. We have recently detected non-nuclear PAR structurally and functionally associated to the E-cadherin rich zonula adherens and the actin cytoskeleton of VERO epithelial cells. Myelinating Schwann cells (SC) are stabilized by E-cadherin rich autotypic adherens junctions (AJ). We wondered whether PAR would map to these regions. Besides, we have demonstrated an altered microfilament pattern in peripheral nerves of Trembler-J (Tr-J) model of CMT1-E. We hypothesized that cytoplasmic PAR would accompany such modified F-actin pattern. Methods. Wild-type (WT) and Tr-J mice sciatic nerves cryosections were subjected to immunohistofluorescence with anti-PAR antibodies (including antibody validation), F-actin detection with a phalloidin probe and DAPI/DNA counterstaining. Confocal image stacks were subjected to a colocalization highlighter and to semi-quantitative image analysis. Results. We have shown for the first time the presence of PAR in sciatic nerves. Cytoplasmic PAR colocalized with F-actin at non-compact myelin regions in WT nerves. Moreover, in Tr-J, cytoplasmic PAR was augmented in close correlation with actin. In addition, nuclear PAR was detected in WT SC and was moderately increased in Tr-J SC. Discussion. The presence of PAR associated to non-compact myelin regions (which constitute E-cadherin rich autotypic AJ /actin anchorage regions) and the co-alterations experienced by PAR and the actin cytoskeleton in epithelium and nerves, suggest that PAR may be a constitutive component of AJ /actin anchorage regions. Is PAR stabilizing the AJ -actin complexes? This question has strong implications in structural cell biology and cell signaling networks. Moreover, if PAR played a stabilizing role, such stabilization could participate in the physiological control of axonal branching. PARP and PAR alterations exist in several neurodegenerative pathologies including Alzheimer's, Parkinson's and Hungtington's diseases. Conversely, PARP inhibition decreases PAR and promotes neurite outgrowth in cortical neurons in vitro. Coherently, the PARP inhibitor XAV939 improves myelination in vitro, ex vivo and in vivo. Until now such results have been interpreted in terms of nuclear PARP activity. Our results indicate for the first time the presence of PARylation in peripheral nerve fibers, in a healthy environment. Besides, we have evidenced a PARylation increase in Tr-J, suggesting that the involvement of cytoplasmic PARPs and PARylation in normal and neurodegenerative conditions should be re-evaluated

    Geotechnical characterization of the upper Pleistocene-Holocene alluvial deposits of Roma (Italy) by means of multivariate geostatistics: Cross-validation results

    Get PDF
    We are presenting an attempt to evaluate the spatial variability of geotechnical parameters in the upper Pleistocene–Holocene alluvial deposits of Roma (Italy) by means of multivariate geostatistics. The upper Pleistocene–Holocene alluvial deposits of Roma are sensitive to high levels of geohazard. They occupy a sizable and significant part of the city, being the foundation for many monuments, historical neighborhoods, and archaeological areas, and the main host of the present and future subway lines. We have stored information from more than 2000 geotechnical boreholes crossing the alluvial deposits into a relational database. For the present study, only the boreholes with lithologic/textural interpretation and geotechnical information were selected. The set includes 283 boreholes and 719 samples, which have a set of geotechnical information comprising physical properties and mechanical parameters. Techniques of multivariate statistics and geostatistics were combined and compared to evaluate the estimation methods of the mechanical parameters, with special reference to the drained friction angle from direct shear test (φ′). Principal Component Analysis was applied to the dataset to highlight the relationships between the geotechnical parameters. Through cross-validation analysis, multiple linear regression, kriging, and cokriging were tested as estimators of φ′. Cross-validation demonstrates that the cokriging with granulometries as auxiliary variables is the most suitable method to estimate φ′. In addition to proving that cokriging is a good estimator of φ′, cross-validation demonstrates that input data are coherent and this allows us to use them for estimation of geotechnical parameters, although they come from different laboratories and different vintages. Nevertheless, to get the same good results of cross-validation in estimation, it is necessary for granulometries to be available at grid points. Since this information being not available at all grid points, it is expected that, in the future, textural information can be derived in an indirect way, i.e., from lithologic/textural spatial reconstructions.Published251-2682.3. TTC - Laboratori di chimica e fisica delle rocceJCR Journalope

    Revealing stage-specific expression patterns of long noncoding RNAs along mouse spermatogenesis

    Get PDF
    The discovery of a large number of long noncoding RNAs (lncRNAs), and the finding that they may play key roles in different biological processes, have started to provide a new perspective in the understanding of gene regulation. It has been shown that the testes express the highest amount of lncRNAs among different vertebrate tissues. However, although some studies have addressed the characterization of lncRNAs along spermatogenesis, an exhaustive analysis of the differential expression of lncRNAs at its different stages is still lacking. Here, we present the results for lncRNA transcriptome profiling along mouse spermatogenesis, employing highly pure flow sorted spermatogenic stage-specific cell populations, strand-specific RNAseq, and a combination of up-to-date bioinformatic pipelines for analysis. We found that the vast majority of testicular lncRNA genes are expressed at post-meiotic stages (i.e. spermiogenesis), which are characterized by extensive post-transcriptional regulation. LncRNAs at different spermatogenic stages shared common traits in terms of transcript length, exon number, and biotypes. Most lncRNAs were lincRNAs, followed by a high representation of antisense (AS) lncRNAs. Co-expression analyses showed a high correlation along the different spermatogenic stage transitions between the expression patterns of AS lncRNAs and their overlapping protein-coding genes, raising possible clues about lncRNA-related regulatory mechanisms. Interestingly, we observed the colocalization of an AS lncRNA and its host sense mRNA in the chromatoid body, a round spermatidsspecific organelle that has been proposed as a reservoir of RNA-related regulatory machinery. An additional, intriguing observation is the almost complete lack of detectable expression for Y-linked testicular lncRNAs, despite that a high number of lncRNA genes are annotated for this chromosom
    corecore