Genótipos de gráo de bico para cultivo na região geoeconômico do Distrito Federal.

Com o objetivo de selecionar genótipos de grão de bico com características agronômicas favoráveis para cultivo na região geoeconômica do Distrito Federal, dez genótipos foram testados: BF 1392 (Espanha), Nacional 29 (Cuba), Jamu 96 (México), Blanco Sinaloa 92 (México), Cícero, CNPH 13127, CNPH 13136, Jolie (Mat. Comercial). Astro (Mat. Comercial), Marrocos (IAC), sendo todos do tipo kabuly.CD-ROM. Suplemento. Trabalho apresentado no 51. Congresso Brasileiro de Olericultura, Viçosa, MG

O Discurso Da Normatização Da Terra

Este artigo discute o processo sócio-histórico e político de apropriação da terra em Mato Grosso, na segunda metade do século XVIII. Produz uma reflexão teórica e metodológica, a partir do discurso da Ata de fundação de Cuiabá, que funciona como o registro oficial de normatização da terra. Nessa materialidade simbólica, o ouro reverbera sentidos, como o elemento que dá estatuto particular a terra, pela geografia do rio Coxipó na cidade de Cuiabá.172114-126Estudos Urbano

Chemical and genetic control of fusarium wilt in chickpea and their effects on stand establishment under tropical conditions.

Abstract 87

First-order structural transition in the multiferroic perovskite-like formate [(CH3)2NH2][Mn(HCOO)3]

In this work we explore the overall structural behaviour of the [(CH3)2NH2][Mn(HCOO)3] multiferroic compound across the temperature range where its ferroelectric transition takes place by means of calorimetry, thermal expansion measurements and variable temperature powder and single crystal X-ray diffraction. The results clearly proof the presence of structural phase transition at Tt ~187 K (temperature at which the dielectric transition occurs) that involves a symmetry change from R-3c to Cc, twinning of the crystals, a discontinuous variation of the unit cell parameters and unit cell volume, and a sharp first-order-like anomaly in the thermal expansion. In addition, the calorimetric results show a 3-fold order-disorder transition. The calculated pressure dependence of the transition temperature is rather large (dTt/dP = 4.6 $\pm$ 0.1 K/kbar), so that it should be feasible to shift it to room temperature using adequate thermodynamic conditions, for instance by application of external pressure

Distribution of indium in the Ánimas - Chocaya - Siete Suyos District

The Ánimas - Chocaya - Siete Suyos district in SW Bolivia hosts a Bolivian-type polymetallic vein mineralization composed mostly of cassiterite, sphalerite, pyrite, galena, stannite, lead sulfosalts, tin sulfosalts and silver sulfosalts. In addition to base (Zn, Sn, Pb) and precious (Ag) metals, important concentrations of In have been described. Systematic EPMA analyses have revealed that the highest concentrations are found in an early generation of sphalerite (up to 9.66 wt% In) and in stannite (up to 4.11 wt% In). Although In-bearing sphalerites are relatively Fe-rich (mostly between 6.0 and 18.1 mol % FeS), the atomic concentrations of these two elements do not yield any correlation. In contrast, In is positively correlated with Cu mostly along a Cu/In = 1 proportion pointing to a (In3+ + Cu+ ) ¿ 2Zn2+ coupled substitution. A relatively high activity of Cu during the crystallization of In-rich sphalerite is also supported by exsolutions of chalcopyrite and stannite.Peer ReviewedPostprint (author's final draft

The Poopó polymetallic epithermal deposit, Bolivia: mineralogy, genetic constraints, and distribution of critical elements

The tin-rich polymetallic epithermal deposit of Poopó, of plausible Late Miocene age, is part of the Bolivian Tin Belt. As an epithermal low sulfidation mineralisation, it represents a typological end-member within the “family” of Bolivian tin deposits. The emplacement of the mineralisation was controlled by the regional fault zone that constitutes the geological border between the Bolivian Altiplano and the Eastern Andes Cordillera. In addition to Sn and Ag, its economic interest resides in its potential in critical elements as In, Ga and Ge. This paper provides the first systematic characterisation of the complex mineralogy and mineral chemistry of the Poopó deposit with the twofold aim of identifying the mineral carriers of critical elements and endeavouring to ascertain plausible metallogenic processes for the formation of this deposit, by means of a multi-methodological approach. The poor development of hydrothermal alteration assemblage, the abundance of sulphosalts and the replacement of löllingite and pyrrhotite by arsenopyrite and pyrite, respectively, indicate that this deposit is ascribed to the low-sulphidation subtype of epithermal deposits, with excursions into higher states of sulphidation. Additionally, the occurrence of pyrophyllite and topaz has been interpreted as the result of discrete pulses of high-sulphidation magmatic fluids. The d34SVCDT range in sulphides (-5.9 to -2.8‰) is compatible either with: (i) hybrid sulphur sources (i.e., magmatic and sedimentary or metasedimentary); or (ii) a sole magmatic source involving magmas that derived from partial melting of sedimentary rocks or underwent crustal assimilation. In their overall contents in critical elements (In, Ga and Ge), the key minerals in the Poopó deposit, based on their abundance in the deposit and compositions, are rhodostannite, franckeite, cassiterite, stannite and, less importantly, teallite, sphalerite and jamesonite.Peer ReviewedPostprint (published version

The Poopó Polymetallic Epithermal Deposit, Bolivia: Mineralogy, Genetic Constraints, and Distribution of Critical Elements

The tin-rich polymetallic epithermal deposit of Poopó, of plausible Late Miocene age, is part of the Bolivian Tin Belt. As an epithermal low sulfidation mineralisation, it represents a typological end-member within the "family" of Bolivian tin deposits. The emplacement of the mineralisation was controlled by the regional fault zone that constitutes the geological border between the Bolivian Altiplano and the Eastern Andes Cordillera. In addition to Sn and Ag, its economic interest resides in its potential in critical elements as In, Ga and Ge. This paper provides the first systematic characterisation of the complex mineralogy and mineral chemistry of the Poopó deposit with the twofold aim of identifying the mineral carriers of critical elements and endeavouring to ascertain plausible metallogenic processes for the formation of this deposit, by means of a multi-methodological approach. The poor development of hydrothermal alteration assemblage, the abundance of sulphosalts and the replacement of löllingite and pyrrhotite by arsenopyrite and pyrite, respectively, indicate that this deposit is ascribed to the low-sulphidation subtype of epithermal deposits, with excursions into higher states of sulphidation. Additionally, the occurrence of pyrophyllite and topaz has been interpreted as the result of discrete pulses of high-sulphidation magmatic fluids. The δ34SVCDT range in sulphides (−5.9 to −2.8 ) is compatible either with: (i) hybrid sulphur sources (i.e., magmatic and sedimentary or metasedimentary); or (ii) a sole magmatic source involving magmas that derived from partial melting of sedimentary rocks or underwent crustal assimilation. In their overall contents in critical elements (In, Ga and Ge), the key minerals in the Poopó deposit, based on their abundance in the deposit and compositions, are rhodostannite, franckeite, cassiterite, stannite and, less importantly, teallite, sphalerite and jamesonite

Indium mineralization in the volcanic dome-hosted Ánimas–Chocaya–Siete Suyos polymetallic deposit, Potosí, Bolivia

A volcanic dome complex of Miocene age hosts the In-bearing Ánimas–Chocaya–Siete Suyos district in SW Bolivia. Ore mineralization occurs as banded and massive infillings in subvertical, NE-SW striking veins. In this article, a detailed petrographic study is combined with in situ mineral geochemistry determinations in ore from the Arturo, Chorro and Diez veins in the Siete Suyos mine, the Ánimas, Burton, Colorada, and Rosario veins in the Ánimas mine and the Nueva vein in the Chocaya mine. A three-stage paragenetic sequence is roughly determined for all of them, and includes (1) an early low-sulfidation stage that is dominated by cassiterite, pyrrhotite, arsenopyrite, and high-Fe sphalerite (FeS > 21 mol. %); (2) a second intermediate-sulfidation stage dominated by pyrite + marcasite ± intermediate product, sphalerite (FeS < 21 mol. %), stannite, and local famatinite; and, (3) a late intermediate-sulfidation stage dominated by galena and Ag-Pb-Sn sulfosalts. Electron-probe microanalyses reveal high indium enrichment in stage-2 sphalerite (up to 9.66 wt.% In) and stannite (up to 4.11 wt.% In), and a moderate enrichment in rare wurtzite (up to 1.61 wt.% In), stage-1 sphalerite (0.35 wt.% In), cassiterite (up to 0.25 wt.% In2O3), and ramdohrite (up to 0.24 wt.% In). Therefore, the main indium mineralization in the district can be associated to the second, intermediate-sulfidation stage, chiefly in those veins in which sphalerite and stannite are more abundant. Atomic concentrations of In and Cu in sphalerite yield a positive correlation at Cu/In = 1 that agrees with a (Cu+ + In3+) ¿ 2Zn2+ coupled substitution. The availability of Cu in the mineralizing fluids during the crystallization of sphalerite is, in consequence, essential for the incorporation of indium in its crystal lattice and would control the distribution of indium enrichment at different scales. The highest concentrations of indium in sphalerite, which is found in the Diez vein in the Siete Suyos mine, occur in crustiform bands of sphalerite with local “chalcopyrite disease” texture, which has not been observed in the other studied veins. In stannite, the atomic concentrations of In are negatively correlated with those of Cu and Sn at Cu + In = 2 and Sn + In = 1. Thus, atomic proportions and correlations suggest the contextualization of the main indium mineralization in the sphalerite–stannite–roquesite pseudoternary system.Peer ReviewedPostprint (published version

DIVERSIDADE GENÉTICA EM GENÓTIPOS DE GIRASSOL NO CERRADO DO PLANALTO CENTRAL.

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