16 research outputs found
Agricultura orgânica: características básicas do seu produtor.
A agricultura orgânica é ainda pouco expressiva no Brasil. Sua relevância é, no entanto, crescente, seguindo tendência observada em outros países, em especial na Europa. Este estudo analisa as características básicas do produtor de produtos orgânicos, contribuindo para preencher uma lacuna existente na literatura de economia rural. Utilizando informações primárias sobre agricultores orgânicos da região próxima à cidade de Curitiba, Paraná, identificamos as suas características pessoais e econômicas, por meio de estatística descritiva, análise de correlação e regressão linear múltipla. Os produtores foram divididos em dois grupos: o primeiro com aqueles que ainda estão em conversão para a agricultura orgânica e o segundo grupo composto por produtores orgânicos que já obtiveram a certificação de seus produtos. Os resultados obtidos indicam que alta participação de capital próprio no financiamento da produção e elevado nível de escolaridade são duas das características mais marcantes dos produtores rurais orgânicos paranaenses. Outras características que influenciam o resultado líquido da atividade são a disponibilidade de mão de obra e a integração de atividades agrícolas, pecuárias e florestais
An Overall Evaluation Of The Resistance (r) And Pathogenesis-related (pr) Super Families In Soybean, As Compared With Medicago And Arabidopsis
Plants have the ability to recognize and respond to a multitude of pathogens, resulting in a massive reprogramming of the plant to activate defense responses including Resistance (R) and Pathogenesis-Related (PR) genes. Abiotic stresses can also activate PR genes and enhance pathogen resistance, representing valuable genes for breeding purposes. The present work offers an overview of soybean Rand PR genes present in the GENOSOJA (Brazilian Soybean Genome Consortium) platform, regarding their structure, abundance, evolution and role in the plant-pathogen metabolic pathway, as compared with Medicago and Arabidopsis. Searches revealed 3,065 R candidates (756 in Soybean, 1,142 in Medicago and 1,167 in Arabidopsis), and PR candidates matching to 1,261 sequences (310, 585 and 366 for the three species, respectively). The identified transcripts were also evaluated regarding their expression pattern in 65 libraries, showing prevalence in seeds and developing tissues. Upon consulting the Super SAGE libraries, 1,072 Rand 481 PR tags were identified in association with the different libraries. Multiple alignments were generated forXa21andPR-2genes, allowing inferences about their evolution. The results revealed interesting insights regarding the variability and complexity of defense genes in soybean, as compared with Medicago and Arabidopsis. © 2012, Sociedade Brasileira de Genética.35SUPPL.1260271Alberts, B., Johnson, A., Lewis, J., Raff, M., Roberts, K., Walter, P., (2002) Molecular Biology of the Cell, p. 1616. , 4th edition. Garland Publishing Company, New York & LondonAltschul, S.F., Gish, W., Miller, W., Myers, E., Basic local alignment search tool (1990) J Mol Biol, 215, pp. 403-410Ashfield, T., Bocian, A., Held, D., Henk, A.D., Marek, L.F., Danesh, D., Penuela, S., Young, N.D., Genetic and physical localization of the soybean Rpg1-b disease resistance gene reveals a complex locus containing several tightly linked families of NBS-LRR genes (2003) Mol Plant Microbe Interact, 16, pp. 817-826Atici, O., Nalbantoglu, B., Antifreeze proteins in higher plants (2003) Phytochemistry, 64, pp. 1187-1196Barbosa-da-Silva, A., Wanderley-Nogueira, A.C., Silva, R.R.M., Belarmino, L.C., Soares-Cavalcanti, N.M., Benko-Iseppon, A.M., In silico survey of resistance (R) genes in Eucalyptus transcriptome (2005) Genet Mol Biol, 28, pp. 562-574Benko-Iseppon, A.M., Galdino, S.L., Calsa, T., Kido, E.A., Tossi, A., Belarmino, L.C., Crovella, S., Overview of plant antimicrobial peptides (2010) Curr Prot Pept Sci, 11, pp. 181-188Bent, A.F., Plant disease resistance genes: Function meets structure (1996) Plant Cell, 8, pp. 1751-1771Bolton, M., Primary metabolism and plant defense-Fuel for the fire (2009) Mol Plant Microbe Interact, 22, pp. 487-497Bonas, U., Anckerveken, G.V., Gene-for-gene interactions: Bacterial avirulence proteins specify plant disease resistance (1999) Curr Opin Plant Biol, 2, pp. 94-98Bonasera, J.M., Kim, J.F., Beer, S.V., PR genes of apple: Identification and expression in response to elicitors and inoculation with Erwinia amylovora (2006) BMC Plant Biol, 6, pp. 23-34Cannon, S.B., May, G.D., Jackson, S.A., Three sequenced legume genomes and many crop species: Rich opportunities for translational genomics (2009) Plant Physiol, 151, pp. 970-977Chester, K.S., The problem of acquired physiological immunity in plants (1933) Quart Rev Phytopathol, 42, pp. 185-209Dafny-Yelin, M., Tzfira, T., Delivery of multiple trans-genes to plant cells (2007) Plant Physiol, 145, pp. 1118-1128Dinesh-Kumar, S.P., Whitham, S., Choi, D., Hehl, R., Corr, C., Baker, B., Transposon tagging of tobacco mosaic virus resistance gene N:I its possible role in the TMV-N-mediated signal transduction pathway (1995) Proc Natl Acad Sci USA, 92, pp. 4175-4180Dixon, M.S., Jones, D.A., Keddie, J.S., Thomas, C.T., Harrison, K., Jones, J.D.G., The tomato Cf2 disease resistance locus comprises two functional genes encoding leucine rich repeats proteins (1996) Cell, 84, pp. 451-459Durrant, W.E., Dong, X., Systemic acquired resistance (2004) Annu Rev Plant Pathol, 42, pp. 185-209Eisen, M.B., Spellman, P.T., Brown, P.O., Botstein, B., Cluster analysis and display of genome-wide expression patterns (1998) Genetics, 25, pp. 14863-14868Ellis, J., Jones, D., Structure and function of proteins controlling strain-specific pathogen resistance in plants (2000) Curr Opin Plant Biol, 1, pp. 288-293Ellis, J., Lawrence, G.J., Finnegan, E.J., Anderson, P.A., Contrasting complexity of two rust resistance loci in flax (1995) Proc Natl Acad Sci USA, 92, pp. 4185-4188Ellis, J., Dodds, P., Pryor, T., Structure, function and evolution of plant disease resistance genes (2000) Curr Opin Plant Biol, 3, pp. 278-284Gaffney, T., Friedrich, L., Vernooij, B., Negrotto, D., Nye, G., Ukness, S., Ward, E., Kessman Hand Ryals, J., Requirementofsalicylic acid for the induction of systemic acquired resistance (1993) Science, 261, pp. 754-756Glombitza, S., Dubuis, P.-H., Thulke, O., Welzl, G., Bovet, L., Götz, M., Affenzeller, M., Asnaghi, C., Crosstalk and differential response to abiotic and biotic stressors reflected at the transcriptional level of effector genes from secondary metabolism (2004) Plant Mol Biol, 54, pp. 817-835Griffith, M., Yaish, M.W.F., Antifreeze proteins in overwintering plants: A tale of two activities (2004) Trends Plant Sci, 9, pp. 399-405Hammond-Kosack, K.E., Jones, J.D.G., Plant disease resistance genes (1997) Annu Rev Plant Physiol, 48, pp. 575-607Hon, W.C., Griffith, M., Mlynarz, A., Kwok, Y.C., Yang, D.S.C., Antifreeze proteins in winter rye are similar to pathogenesis-related proteins (1995) Plant Physiol, 109, pp. 879-889Hulbert, S.H., Webb, C.A., Smith, S.M., Sun, Q., Resistance gene complexes: Evolution and utilization (2001) Annu Rev Phytopathol, 39, pp. 285-312Joahal, G.S., Briggs, S.P., Reductase activity encodes by the Hm1 resistance gene in maize (1992) Science, 198, pp. 985-987Kanazin, V., Marek, L.F., Shoemaker, R.C., Resistance gene analogs are conserved and clustered in soybean (1996) Proc Natl Acad Sci USA, 93, pp. 11746-11750Kido, E.A., Barbosa, P.K., Ferreira Neto, J.C.R., Pandolfi, V., Houllou-Kido, L.M., Crovella, S., Benko-Iseppon, A.M., Identification of plant protein kinases in response to abiotic and biotic stresses using Super SAGE (2011) Curr Prot Pept Sci, 12, pp. 643-656Kitajima, S., Sato, F., Plant pathogenesis-related proteins: Molecular mechanisms of gene expression and protein function (1999) J Biochem, 125, pp. 1-8Lavin, M., Herendeen, P.S., Wojciechowski, M.F., Evolutionary rates analysis of Leguminosae implicates a rapid diversification of lineages during the tertiary (2005) Syst Biol, 54, pp. 575-594Lawrence, G.J., Finnegan, E.J., Ayliffe, M.A., Ellis, J.G., The L6 gene for flax rust resistance is related to the Arabidopsis bacterial resistance gene RPS2 and the tobacco viral resistance gene (1995) N. Plant Cell, 7, pp. 1195-1206Leubner-Metzger, G., β-1,3-glucanase gene expression in low-hydrated seeds as a mechanism for dormancy release during tobacco after-ripening (2005) Plant J, 41, pp. 133-145Li, L., He, H., Zhang, J., Wang, X., Bai, S., Stolc, V., Tongprasit, W., Deng, X.W., Transcriptional analysis of highly syntenic regions between Medicago truncatula and Glycine max using tiling microarrays (2008) Genome Biol, 9, pp. R57Libault, M., Farmer, A., Joshi, T., Takahashi, K., Langley, R.J., Franklin, L.D., He, J., Stacey, G., An integrated transcriptome atlas of the crop model Glycine max and its use in comparative analyses in plants (2010) Plant J, 63, pp. 86-99Liu, B., Zhang, S., Zhu, X., Yang, Q., Wu, S., Mei, M., Mauleon, R., Leung, H., Candidate defense genes as predictors of quantitative blast resistance in rice (2004) Mol Plant Microbe Int, 17, pp. 1146-1152Maisonneuve, B., Bellec, Y., Anderson, P., Michelmore, R.W., Rapid mapping of two genes for resistance to downy mildew from Lactuca serriola to existing clusters of resistance genes (1994) Theor Appl Genet, 89, pp. 96-104Matsumura, H., Kruger, D.H., Kahl, G., Terauchi, R., SuperSAGE: A modern platform for genome-wide quantitative transcript profiling (2008) Curr Pharm Biotechnol, 9, pp. 368-374Melotto, M., Coelho, M.F., Pedrosa-Harand, A., Kelly, J.D., Camargo, L.E., The anthracnose resistance locus Co-4 of common bean is located on chromosome 3 and contains putative disease resistance-related genes (2004) Theor Appl Genet, 109, pp. 690-699Metzler, M.C., Cutt, J.R., Klessig, D.F., Isolation and characterization of a gene encoding a PR-1 like protein from Arabidopsis thaliana (1991) Plant Physiol, 96, pp. 346-348Michelmore, R.W., Meyers, B.C., Clusters of resistance genes in plants evolve by divergent selection and a birth-and-death process (1998) Genome Res, 8, pp. 1113-1130Mindrinos, M., Katagiri, F., Yu, G.L., Ausubel, F.M., The Arabidopsis thaliana disease resistance gene encodes a protein containing a nucleotide-binding site and leucine rich repeats (1994) Cell, 78, pp. 1089-1099Mudge, J., Cannon, S.B., Kalo, P., Oldroyd, G.E., Roe, B.A., Town, C.D., Young, N.D., Highly syntenic regions in the genomes of soybean, Medicago truncatula and Arabidopsis thaliana (2005) BMC Plant Biol, 5, pp. e15Nanda, A.K., Andrio, E., Marino, D., Pauly, N., Dunand, C., Reactive Oxygen Species during plant-microorganism early interactions (2010) J Integr Plant Biol, 52, pp. 195-204Nurnberg, T., Brunner, F., Innate immunity in plants and animals: Emerging parallels between the recognition of general elicitors and pathogen-associated molecular patterns (2002) Curr Opin Plant Biol, 5, pp. 318-324Page, R.D., (1996) Comp Appl Biosci, 12, pp. 357-358Rayapati, P.J., Lee, M., Gregory, J.W., Wise, R.P., A linkage map of diploid Avena based on RFLP loci and a locus conferring resistance to nine isolates of Puccinia coronata var. 'avenae' (1994) Theor Appl Genet, 89, pp. 831-837Salmeron, J.M., Oldroyd, G.E.D., Romens, C.M.T., Scofield, S.R., Kim, H.S., Lavelle, D.T., Dahlbeck, D., Staskawicz, B.J., Tomato Prf is a member of the leucine rich repeats class of plant disease resistance genes and lies embedded within the Pto kinase gene cluster (1996) Cell, 86, pp. 123-133Shoemaker, R.C., Schlueter, J., Doyle, J.J., Paleopolyploidy and gene duplication in soybean and other legumes (2006) Curr Opin Plant Biol, 9, pp. 104-109Song, W.Y., Pi, L.Y., Wang, G.L., Gardner, J., Holsten, T., Ronald, P.C., Evolution of the rice Xa21 disease resistance genes family (1997) Plant Cell, 9, pp. 1279-1287Song, W.Y., Wang, G.L., Kim, H.S., Pi, L.Y., Gardner, J., Wang, B., Holsten, T., Fauquet, C., A receptor kinase-like protein encoded by the rice disease resistance gene Xa21 (1995) Science, 270, pp. 1804-1806Sparla, F., Rotino, L., Valgimigli, M.C., Pupillo, P., Trost, P., Systemic resistance induced by benzothisdizole in pear inoculated with the agent of fire blight (2004) Sci Hortic, 101, pp. 269-279Tamura, K., Dudley, J., Nei, M., Kumar, S., MEGA4: Molecular Evolutionary Genetics Analysis (MEGA) software ver. 4.0 (2007) Mol Biol Evol, 24, pp. 1596-1599Tang, X., Xie, M., Kim, Y.J., Zhou, J., Klessing, D.F., Martin, G.B., Overexpression of Pto activates defense responses and confers broad resistance (1999) Plant Cell, 11, pp. 15-29Thiel, T., Graner, A., Waugh, R., Grosse, I., Close, T.J., Stein, N., Evidence and evolutionary of ancient whole-genome duplication in barley predating the divergence from rice (2009) BMC Evol Biol, 9, pp. 209-227Tornero, P., Gadea, J., Conejero, V., Vera, P., Two PR-1 genes from tomato are differentially regulated and reveal a novel mode of expression for a pathogenesis-related gene during the hypersensitive response and development (1997) Plant Microbe Interact, 10, pp. 624-634Van-Loon, L.C., Geraats, B.P.J., Linthorst, H.J.M., Ethylene as a modulator of disease resistance in plants (2006) Trends Plant Sci, 11, pp. 184-191Van-Loon, L.C., Pierpoint, W.S., Boller, T., Conejero, V., Recommendations for naming plant pathogenesis-related proteins (1999) Plant Mol Biol Rep, 12, pp. 245-264Velazhahan, R., Muthukrishnan, S., Transgenic tobacco plants constitutively overexpressing a rice thaumatin-like protein (PR-5) show enhanced resistance to Alternaria alternata (2003) Plant Biol, 47, pp. 347-354Vergne, E., Grand, X., Ballini, R., Chalvon, V., Saindrenan, P., Tharreau, D., Nottéghem, J.-L., Morel, J.-B., Preformed expression of defense is a hallmark of partial resistance to rice blast fungal pathogen Magnaporthe oryzae (2010) BMC Plant Biol, 10, pp. e206Wanderley-Nogueira, A.C., Mota, N., Lima-Morais, D., Silva, L.C.B., Silva, A.B., Benko-Iseppon, A.M., Abundance and diversity of resistance (R) genes in the sugarcane trans-criptome (2007) Genet Mol Res, 6, pp. 866-889Wang, G.L., Holsten, T.E., Song, W.Y., Wang, H.P., Ronald, P.C., Construction of a rice bacterial artificial chromosome library and identification of clones linked to the Xa21 disease resistance locus (1995) Plant J, 7, pp. 525-533Wendell, J., Genome evolution in polyploids (2000) Plant Mol Biol, 42, pp. 225-249Weng, J.K., Banks, J.A., Chapple, C., Parallels in lignin biosynthesis: A study in Selaginella moellendorffii reveals convergence across 400 million years of evolution (2008) Comm Int Biol, 1, pp. 20-22Wilkstrom, N., Savolainen, V., Chase, M.W., Evolution of the angiosperms: Calibrating the family tree (2001) Proc Soc Biol Sci, 268, pp. 2211-2220Zeier, J., Pink, B., Mueller, M.J., Berger, S., Light conditions influence specific defense responses in incompatible plant-pathogen interactions: Uncoupling systemic resistance from salicylic acid and PR-1 accumulation (2004) Planta, 219, pp. 673-68
Informações biológicas e estimativa do tamanho ideal da colmeia para a abelha tiúba do Maranhão (Melipona compressipes fasciculata Smith - Hymenoptera, Apidae)
ANÁLISE SILVICULTURAL E ECONÔMICA DE PLANTIOS CLONAIS E SEMINAIS DE Tectona grandis L.f. EM SISTEMA TAUNGYA1
RESUMO O objetivo deste estudo foi realizar uma análise silvicultural e econômica de plantios clonais e seminais de Tectona grandis em monocultivo e em sistema taungya com Zea mays, no Município de Figueirópolis D'Oeste, MT. O experimento foi instalado em 2010 e compôs um fatorial 2x2 em blocos casualizados e quatro repetições. Avaliaram-se a altura total (H), o diâmetro a 5 cm (DAB) e a 1,3 m (DAP) de altura em relação ao nível do solo, a área basal, o volume, a sobrevivência e a estimativa e tendência de crescimento da teca na idade atual e futura, além da produção de silagem do milho. Foram realizadas análises das receitas e custos totais de implantação e manutenção do sistema. Plantas clonais em monocultivo e no sistema Taungya apresentaram maior crescimento em altura total, DAB e DAP em relação às seminais. No monocultivo e no sistema Taungya, a produção (m3 ha-1) de plantas clonais em relação às seminais foi 33 e 30% superior, respectivamente. Os custos com insumos e atividades de implantação da teca foram superiores e os de manutenção, inferiores no sistema Taungya em relação ao monocultivo, tanto para plantios clonais quanto seminais. No sistema Taungya com plantas clonais, o milho reduziu em 21% os custos totais de implantação e manutenção em relação ao monocultivo; nas plantas seminais, a redução foi de 27%. A teca no sistema Taungya cresce menos, porém apresenta tendência de recuperação após a retirada do milho, cuja presença amortiza custos de implantação e manutenção da teca em plantios clonais e seminais
Modelagem estatística para estimação da população de protozoários ruminais em função da relação volumoso: concentrado na dieta e da presença de aditivos
J-PLUS: The javalambre photometric local universe survey
ABSTRACT: TheJavalambrePhotometric Local UniverseSurvey (J-PLUS )isanongoing 12-band photometricopticalsurvey, observingthousands of squaredegrees of theNorthernHemispherefromthededicated JAST/T80 telescope at the Observatorio Astrofísico de Javalambre (OAJ). The T80Cam is a camera with a field of view of 2 deg2 mountedon a telescopewith a diameter of 83 cm, and isequippedwith a uniquesystem of filtersspanningtheentireopticalrange (3500–10 000 Å). Thisfiltersystemis a combination of broad-, medium-, and narrow-band filters, optimallydesigned to extracttherest-framespectralfeatures (the 3700–4000 Å Balmer break region, Hδ, Ca H+K, the G band, and the Mg b and Ca triplets) that are key to characterizingstellartypes and delivering a low-resolutionphotospectrumforeach pixel of theobservedsky. With a typicaldepth of AB ∼21.25 mag per band, thisfilter set thusallowsforanunbiased and accuratecharacterization of thestellarpopulation in our Galaxy, itprovidesanunprecedented 2D photospectralinformationforall resolved galaxies in the local Universe, as well as accuratephoto-z estimates (at the δ z/(1 + z)∼0.005–0.03 precisionlevel) formoderatelybright (up to r ∼ 20 mag) extragalacticsources. Whilesomenarrow-band filters are designedforthestudy of particular emissionfeatures ([O II]/λ3727, Hα/λ6563) up to z < 0.017, theyalsoprovidewell-definedwindowsfortheanalysis of otheremissionlines at higherredshifts. As a result, J-PLUS has thepotential to contribute to a widerange of fields in Astrophysics, both in thenearbyUniverse (MilkyWaystructure, globular clusters, 2D IFU-likestudies, stellarpopulations of nearby and moderate-redshiftgalaxies, clusters of galaxies) and at highredshifts (emission-line galaxies at z ≈ 0.77, 2.2, and 4.4, quasi-stellarobjects, etc.). Withthispaper, wereleasethefirst∼1000 deg2 of J-PLUS data, containingabout 4.3 millionstars and 3.0 milliongalaxies at r < 21mag. With a goal of 8500 deg2 forthe total J-PLUS footprint, thesenumbers are expected to rise to about 35 millionstars and 24 milliongalaxiesbytheend of thesurvey.Funding for the J-PLUS Project has been provided by the Governments of Spain and Aragón through the Fondo de Inversiones de Teruel, the Spanish Ministry of Economy and Competitiveness (MINECO; under grants AYA2017-86274-P, AYA2016-77846-P, AYA2016-77237-C3-1-P, AYA2015-66211-C2-1-P, AYA2015-66211-C2-2, AYA2012-30789, AGAUR grant SGR-661/2017, and ICTS-2009-14), and European FEDER funding (FCDD10-4E-867, FCDD13-4E-2685
NEOTROPICAL XENARTHRANS: a data set of occurrence of xenarthran species in the Neotropics
Xenarthrans – anteaters, sloths, and armadillos – have essential functions for ecosystem maintenance, such as insect control and nutrient cycling, playing key roles as ecosystem engineers. Because of habitat loss and fragmentation, hunting pressure, and conflicts with 24 domestic dogs, these species have been threatened locally, regionally, or even across their full distribution ranges. The Neotropics harbor 21 species of armadillos, ten anteaters, and six sloths. Our dataset includes the families Chlamyphoridae (13), Dasypodidae (7), Myrmecophagidae (3), Bradypodidae (4), and Megalonychidae (2). We have no occurrence data on Dasypus pilosus (Dasypodidae). Regarding Cyclopedidae, until recently, only one species was recognized, but new genetic studies have revealed that the group is represented by seven species. In this data-paper, we compiled a total of 42,528 records of 31 species, represented by occurrence and quantitative data, totaling 24,847 unique georeferenced records. The geographic range is from the south of the USA, Mexico, and Caribbean countries at the northern portion of the Neotropics, to its austral distribution in Argentina, Paraguay, Chile, and Uruguay. Regarding anteaters, Myrmecophaga tridactyla has the most records (n=5,941), and Cyclopes sp. has the fewest (n=240). The armadillo species with the most data is Dasypus novemcinctus (n=11,588), and the least recorded for Calyptophractus retusus (n=33). With regards to sloth species, Bradypus variegatus has the most records (n=962), and Bradypus pygmaeus has the fewest (n=12). Our main objective with Neotropical Xenarthrans is to make occurrence and quantitative data available to facilitate more ecological research, particularly if we integrate the xenarthran data with other datasets of Neotropical Series which will become available very soon (i.e. Neotropical Carnivores, Neotropical Invasive Mammals, and Neotropical Hunters and Dogs). Therefore, studies on trophic cascades, hunting pressure, habitat loss, fragmentation effects, species invasion, and climate change effects will be possible with the Neotropical Xenarthrans dataset
