989 resultados para rendimento clonal


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Este experimento foi realizado no Campo Experimental de Bebedouro, da Embrapa Semi-Árido, em Petrolina-PE, de janeiro de 1999 a dezembro de 2001, num Argissolo Amarelo eutrófico textura arenosa, com o objetivo de avaliar o efeito de adubos verdes associados à calagem e adubação mineral e orgânica nos atributos químicos do solo e na produtividade e qualidade do melão (Cucumis melo) irrigado. O delineamento experimental foi de blocos casualizados, em esquema de parcelas subdivididas, com quatro repetições. Os tratamentos alocados nas parcelas constituíram-se dos adubos verdes: (1) milho (Zea mays) com retirada da palhada do local, como testemunha (MI); (2) mucuna-preta (Mucuna aterrima) (MP); (3) milho + caupi (Vigna unguiculata) (MC); e (4) adubos verdes diferentes em cada ano: dois cultivos sucessivos de crotalária (Crotalaria juncea) no primeiro ano, milheto (Pennisetum glaucum) + caupi no segundo e crotalária + caupi no terceiro (RA). Nas subparcelas, os tratamentos corresponderam a: dose completa de calagem e adubação mineral e orgânica conforme a análise do solo (DC); e metade da dose do tratamento anterior (MD). Os cultivos dos adubos verdes foram realizados no primeiro semestre, seguidos do cultivo do melão no segundo. Todos os adubos verdes proporcionaram aumentos nos valores de Ca e da CTC do solo nas camadas de 0?10 cm e 10?20 cm em relação à testemunha (MI), com exceção da MP para CTC na primeira profundidade. Na camada de 0?10 cm, houve aumento também nos teores de K e matéria orgânica do solo, exceto nos teores de K do MC. Em 2001, ano em que o meloeiro atingiu a maior produtividade, o adubo verde RA proporcionou maior rendimento de melão que o adubo MP e a testemunha. Da mesma forma, o tratamento DC promoveu maior produtividade que o MD. Nesse mesmo ano, os teores de sólidos solúveis totais dos frutos foram mais elevados no tratamento com MP que na testemunha.

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Foi instalado um ensaio de avaliação de 73 progênies do Programa de Melhoramento de mamona do Instituto Agronômico para dias para florescimento dos racemos, produção de grãos e rendimento de grãos, em Campinas-SP, em fevereiro, e avaliado na safrinha de 2007, em blocos casualisados com três repetições, incluindo sete testemunhas comerciais. A análise de variância e a distribuição de médias para produção de grãos evidenciaram a larga variabilidade e o potencial dos materiais para o melhoramento. As progênies mais produtivas foram: PB72II com 804,07 g; PB05II com 755,20 g; TS38 com 716,13 g; PB08II com 714,67 g e PB48 com 698,00 g, e não foram melhores que a testemunha mais produtiva, IAC 2028 com 1019,67 g. Os rendimentos no processamento das sementes foram bastante variados e refletiram a ocorrência de déficits hídricos de severidade moderada, com alto número de sementes chochas ou não granadas. Os resultados mostraram o elevado potencial para o melhoramento do conjunto de progênies estudado e a possibilidade de plantio da cultura da mamona em condição de safrinha no Sudeste do Brasil.

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A seleção clonal supõe que o cultivo prolongado de uma determinada variedade origina variabilidade nos indivíduos daquela população. O presente trabalho teve por objetivo prospectar e identificar plantas de variedades viníferas com base em suas características morfológicas, fenológicas e fitossanitárias em vinhedos antigos.

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Classical myeloproliferative neoplasms (MPNs) are hematopoietic stem cell disorders that manifest with inflammation, promotion of atherosclerosis, hypercoagulability, fibrosis, and clonal evolution. The complex biological background lends itself to multi-omics studies. We have previously shown that reduced platelet fibrinogen receptor (PFR) expression may follow hyperactivation of plasma-dependent mechanisms, such as tissue factor (TF) release, unbalanced thrombin generation, involvement of protease-activated receptors (PARs). Acetylsalicylic acid (ASA) helped to restore the expression of PFRs. In this study, we enrolled 53 MPN patients, subjecting them to advanced genetic testing (panel of 30 genes in NGS), global coagulation testing (Rotational Thromboelastometry - ROTEM) and cytofluorometric determination of PFRs. ROTEM parameters appear to differ considerably depending on the type of pathology under investigation, cell count, and selected mutations. Essential thrombocythemia (ET) and CALR mutation appear to correlate with increased efficiency of both classical coagulation pathways, with significantly more contracted clot formation times (CFTs). In contrast, primary myelofibrosis (PMF) and polycythemia vera (PV) show greater imbalances in the hemostatic system. PV, probably due to its peculiar hematological features, shows a lengthening of the CFT and, at the same time, a selective contraction of parameters in INTEM with the increase of platelets and white blood cells. PMF - in contrast - seems to exploit the extrinsic pathway more to increase cell numbers. The presence of DNMT3A mutations is associated with reduced clotting time (CT) in EXTEM, while ASXL1 causes reduced maximal lysis (ML). EZH2 could be responsible for the elongation of CFT in INTEM assay. In addition, increased PFR expression is associated with history of hemorrhage and sustained CT time in FIBTEM under ASA prophylaxis. Our findings corroborate the existing models on the connection between fibrosis, genetic complexity, clonal progression, and hypercoagulability. Global coagulation assays and PFR expression are potentially useful tools for dynamic evaluation of treatments’ outcomes.

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Avian pathogenic Escherichia coli (APEC) strains belong to a category that is associated with colibacillosis, a serious illness in the poultry industry worldwide. Additionally, some APEC groups have recently been described as potential zoonotic agents. In this work, we compared APEC strains with extraintestinal pathogenic E. coli (ExPEC) strains isolated from clinical cases of humans with extra-intestinal diseases such as urinary tract infections (UTI) and bacteremia. PCR results showed that genes usually found in the ColV plasmid (tsh, iucA, iss, and hlyF) were associated with APEC strains while fyuA, irp-2, fepC sitDchrom, fimH, crl, csgA, afa, iha, sat, hlyA, hra, cnf1, kpsMTII, clpVSakai and malX were associated with human ExPEC. Both categories shared nine serogroups (O2, O6, O7, O8, O11, O19, O25, O73 and O153) and seven sequence types (ST10, ST88, ST93, ST117, ST131, ST155, ST359, ST648 and ST1011). Interestingly, ST95, which is associated with the zoonotic potential of APEC and is spread in avian E. coli of North America and Europe, was not detected among 76 APEC strains. When the strains were clustered based on the presence of virulence genes, most ExPEC strains (71.7%) were contained in one cluster while most APEC strains (63.2%) segregated to another. In general, the strains showed distinct genetic and fingerprint patterns, but avian and human strains of ST359, or ST23 clonal complex (CC), presented more than 70% of similarity by PFGE. The results demonstrate that some zoonotic-related STs (ST117, ST131, ST10CC, ST23CC) are present in Brazil. Also, the presence of moderate fingerprint similarities between ST359 E. coli of avian and human origin indicates that strains of this ST are candidates for having zoonotic potential.

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Metastasizing pleomorphic adenoma (MPA) is a rare tumour, and its mechanism of metastasis still is unknown. To date, there has been no study on MPA genomics. We analysed primary and secondary MPAs with array comparative genomic hybridization to identify somatic copy number alterations and affected genes. Tumour DNA samples from primary (parotid salivary gland) and secondary (scalp skin) MPAs were subjected to array comparative genomic hybridization investigation, and the data were analysed with NEXUS COPY NUMBER DISCOVERY. The primary MPA showed copy number losses affecting 3p22.2p14.3 and 19p13.3p123, and a complex pattern of four different deletions at chromosome 6. The 3p deletion encompassed several genes: CTNNB1, SETD2, BAP1, and PBRM1, among others. The secondary MPA showed a genomic profile similar to that of the primary MPA, with acquisition of additional copy number changes affecting 9p24.3p13.1 (loss), 19q11q13.43 (gain), and 22q11.1q13.33 (gain). Our findings indicated a clonal origin of the secondary MPA, as both tumours shared a common profile of genomic copy number alterations. Furthermore, we were able to detect in the primary tumour a specific pattern of copy number alterations that could explain the metastasizing characteristic, whereas the secondary MPA showed a more unbalanced genome.