Effects of the orientation of the mountainside, altitude and varieties on the quality of the coffee beverage from the "Matas de Minas" region, brazilian Southeast.

Based upon qualitative parameters experiments, this study aims to investigate how the elements of the environment, where the coffee is produced, contribute to the final quality of the product. For the analyses, it was used approximately one kilogram of coffee cherry samples collected in 14municipalities previously chosen on the East side of the Minas Gerais State, Brazil. The coffee cherry samples were collected and analyzed for each of the two varieties in four levels of altitude for each exposure side of the mountain in relation to the Sun. The quality of the coffee was evaluated through the analysis of its physical characteristics and sensory analysis, popularly known as "Test of drink or Cupping" carried out by three tasters that belonging to the group of Q -Graders, according to the rules of national and international competitions of the Brazilian Association of Special Coffees (BSCA). Were performed analysis by means descriptive statistics, analysis of variance and multivariate analysis, all of them aiming to study the individual sensor y characteristics of quality of the coffee beverage from the ?Matas de Minas? region. Path coefficient analysis also was carried out for the partition of the phenotypic correlation coefficients into measures of direct and indirect effects, in order to determine the individual sensory characteristics that playeda major role in the beverage final score. The results demonstrat e that it is not possible to concl usively establish the differences among coffees evaluated with basis on varieties and environmental factors previously cited. It can be concluded that it is not recommended to associate the quality of coffee only to a specific factor whether from the environment or being it a specific of the culture of coffee. However, the cafes that were evaluated had intrinsic quality, which were derived from the specific characteristics of the ?Matas de Minas? region where they were grown.

Chemistry, Raman and infrared spectroscopic characterization of the phosphate mineral reddingite: (MnFe)3(PO4)2(H2O,OH)3, a mineral found in lithium-bearing pegmatite

Detailed investigation of an intermediate member of the reddingite–phosphoferrite series, using infrared and Raman spectroscopy, scanning electron microcopy and electron microprobe analysis, has been carried out on a homogeneous sample from a lithium-bearing pegmatite named Cigana mine, near Conselheiro Pena, Minas Gerais, Brazil. The determined formula is (Mn1.60Fe1.21Ca0.01Mg0.01)∑2.83(PO4)2.12⋅(H2O2.85F0.01)∑2.86 indicating predominance in the reddingite member. Raman spectroscopy coupled with infrared spectroscopy supports the concept of phosphate, hydrogen phosphate and dihydrogen phosphate units in the structure of reddingite-phosphoferrite. Infrared and Raman bands attributed to water and hydroxyl stretching modes are identified. Vibrational spectroscopy adds useful information to the molecular structure of reddingite–phosphoferrite.

A vibrational spectroscopic study of the phosphate mineral zanazziite - Ca2(MgFe2+)(MgFe2+Al)4Be4(PO4)6⋅6(H2O)

Zanazziite is the magnesium member of a complex beryllium calcium phosphate mineral group named roscherite. The studied samples were collected from the Ponte do Piauí mine, located in Itinga, Minas Gerais. The mineral was studied by electron microprobe, Raman and infrared spectroscopy. The chemical formula can be expressed as Ca2.00(Mg3.15,Fe0.78,Mn0.16,Zn0.01,Al0.26,Ca0.14)Be4.00(PO4)6.09(OH)4.00⋅5.69(H2O) and shows an intermediate member of the zanazziite–greinfeinstenite series, with predominance of zanazziite member. The molecular structure of the mineral zanazziite has been determined using a combination of Raman and infrared spectroscopy. A very intense Raman band at 970 cm−1 is assigned to the phosphate symmetric stretching mode whilst the Raman bands at 1007, 1047, 1064 and 1096 cm−1 are attributed to the phosphate antisymmetric stretching mode. The infrared spectrum is broad and the antisymmetric stretching bands are prominent. Raman bands at 559, 568, 589 cm−1 are assigned to the ν4 out of plane bending modes of the PO4 and HPO4 units. The observation of multiple bands supports the concept that the symmetry of the phosphate unit in the zanazziite structure is reduced in symmetry. Raman bands at 3437 and 3447 cm−1 are attributed to the OH stretching vibrations; Raman bands at 3098 and 3256 are attributed to water stretching vibrations. The width and complexity of the infrared spectral profile in contrast to the well resolved Raman spectra, proves that the pegmatitic phosphates are better studied with Raman spectroscopy.

Vibrational spectroscopic characterization of the phosphate mineral hureaulite – (Mn, Fe)5(PO4)2(HPO4)2·4(H2O)

This research was done on hureaulite samples from the Cigana claim, a lithium bearing pegmatite with triphylite and spodumene. The mine is located in Conselheiro Pena, east of Minas Gerais. Chemical analysis was carried out by Electron Microprobe analysis and indicated a manganese rich phase with partial substitution of iron. The calculated chemical formula of the studied sample is: (Mn3.23, Fe1.04, Ca0.19, Mg0.13)(PO4)2.7(HPO4)2.6(OH)4.78. The Raman spectrum of hureaulite is dominated by an intense sharp band at 959 cm−1 assigned to PO stretching vibrations of HPO42− units. The Raman band at 989 cm−1 is assigned to the PO43− stretching vibration. Raman bands at 1007, 1024, 1047, and 1083 cm−1 are attributed to both the HOP and PO antisymmetric stretching vibrations of HPO42− and PO43− units. A set of Raman bands at 531, 543, 564 and 582 cm−1 are assigned to the ν4 bending modes of the HPO42− and PO43− units. Raman bands observed at 414, and 455 cm−1 are attributed to the ν2 HPO42− and PO43− units. The intense A series of Raman and infrared bands in the OH stretching region are assigned to water stretching vibrations. Based upon the position of these bands hydrogen bond distances are calculated. Hydrogen bond distances are short indicating very strong hydrogen bonding in the hureaulite structure. A combination of Raman and infrared spectroscopy enabled aspects of the molecular structure of the mineral hureaulite to be understood.

Reply to the comments on “A study of the phosphate mineral kapundaite NaCa(Fe3+)4(PO4)4(OH)3·5(H2O) using SEM/EDX and vibrational spectroscopic methods” by Frost et al. (2014)

"The authors agree with the statements made by Mills and Christy on the study of kapundaite [1]. These authors are correct and have removed any confusion about the origin of the sample kapundaite. The authors (Frost et al.) confirm the sample of kapundaite studied in this work is from the Tom‘s quarry, Australia and can be considered a type material. The authors do not accept the statements by Mills and Christy on “type minerals”. The sample of kapundaite from the Australian source is from the collection of the Geology Department of the Federal University of Ouro Preto, Minas Gerais, Brazil with sample code SAC-111. At least if our mineral sample is not a co-type mineral, our sample is from the same origin as the type mineral. Samples..."--publisher website.

The molecular structure of the phosphate mineral beraunite Fe2+Fe⅗+(PO4)4(OH)5⋅4H2O– A vibrational spectroscopic study

The mineral beraunite from Boca Rica pegmatite in Minas Gerais with theoretical formula Fe2+Fe5 3+(PO4)4(OH)5⋅4H2O has been studied using a combination of electron microscopy with EDX and vibrational spectroscopic techniques. Raman spectroscopy identifies an intense band at 990 cm-1 and 1011 cm-1. These bands are attributed to the PO4 3- v, symmetric stretching mode. The m3 antisymmetric stretching modes are observed by a large number of Raman bands. The Raman bands at 1034, 1051, 1058, 1069 and 1084 together with the Raman bands at 1098, 1116, 1133, 1155 and 1174 cm-1 are assigned to the m3 antisymmetric stretching vibrations of PO4 3- and the HOPO3 2- units. The observation of these multiple Raman bands in the symmetric and antisymmetric stretching region gives credence to the concept that both phosphate and hydrogen phosphate units exist in the structure of beraunite. The series of Raman bands at 567, 582,601, 644, 661, 673, and 687 cm-1 are assigned to the PO4 3- v2 bending modes. The series of Raman bands at 437, 468, 478, 491, 503 cm-1 are attributed to the PO4 3- and OPO3 2- v4 bending modes. No Raman bands of beraunite which could be attributed to the hydroxyl stretching unit were observed. Infrared bands at 3511 and 3359 cm-1 are ascribed to the OH stretching vibration of the OH units. Very broad bands at 3022 and 3299 cm-1 are attributed to the OH stretching vibrations of water. Vibrational spectroscopy offers insights into the molecular structure of the phosphate mineral beraunite.

Raman and infrared spectroscopic study of the borate mineral kaliborite

We have studied the mineral kaliborite. The sample originated from the Inder B deposit, Atyrau Province, Kazakhstan, and is part of the collection of the Geology Department of the Federal University of Ouro Preto, Minas Gerais, Brazil. The mineral is characterized by a single intense Raman band at 756 cm−1 assigned to the symmetric stretching modes of trigonal boron. Raman bands at 1229 and 1309 cm−1 are assigned to hydroxyl in-plane bending modes of boron hydroxyl units. Raman bands are resolved at 2929, 3041, 3133, 3172, 3202, 3245, 3336, 3398, and 3517 cm−1. These Raman bands are assigned to water stretching vibrations. A very intense sharp Raman band at 3597 cm−1 with a shoulder band at 3590 cm−1 is assigned to the stretching vibration of the hydroxyl units. The Raman data are complimented with infrared data and compared with the spectrum of kaliborite downloaded from the Arizona State University database. Differences are noted between the spectrum obtained in this work and that from the Arizona State University database. This research shows that minerals stored in a museum mineral collection age with time. Vibrational spectroscopy enhances our knowledge of the molecular structure of kaliborite.

Temas de historia argentina y americana, 2008, n° 13 (número completo)

De la casa al partido y del partido al hogar (1946-1955) / Carolina Barry -- Un nuevo espacio de poder: las milicias en San Luis Potosí a finales del período colonial (1767-1810) / Juan José Benavides Martínez -- Proscripción y exilio. Ofensiva judicial / Federico Bertram y Sandra Villa -- La traslación española hacia América durante la segunda mitad del siglo XIX / Rosario Güenaga -- La Catedral en la Penitenciaría. Historia de un fastuoso proyecto urbanístico para Buenos Aires (1934) / Miranda Lida -- Aportes de la arqueología subacuática: el naufragio de la fragata española San Salvador (1812) / Atilio Nasti -- Las familias nativas de la Ciudad de Buenos Aires antes de la gran inmigración / Cristian Redi -- El naufragio de la cazatorpedera Rosales (1892): juicio al comandante Leopoldo Funes / Guillermo Oyarzábal -- La disputa por la argentinidad. Rupturistas y neutralistas durante la Primera Guerra Mundial / María Inés Tato -- Reseñas Bibliográficas

Monseñor Pablo Cabrera : escritura de la historia y vínculos intelectuales a principios del siglo XX

Resumen: La emergencia de una historia que reivindicaba el período colonial a principios del siglo XX se desarrolló en un contexto de revisión de la historia nacional, donde se buscaba reafirmar la identidad en un escenario caracterizado por la fuerte presencia de la inmigración en la sociedad argentina. Estos estudios coloniales formaron parte, a su vez, de la difusión de la corriente hispanista e Indigenista en América Latina. Todo esto llevó al desarrollo de un entramado de relaciones intelectuales de las que formó parte Monseñor Pablo Cabrera —1857-1936— en tanto sacerdotehistoriador cordobés que centró sus investigaciones en la historia colonial. En este artículo centraré mi análisis en los estudios históricos de Monseñor Cabrera sobre el período colonial y la relación especial con intelectuales de la Provincia de Santa Fe como Ramón Lassaga y Manuel Cervera

Eli, Eli, Lama Shabaqtani” la condición cristiana en el Medio Oriente

Resumen: El artículo enfoca la situación de los cristianos del Medio Oriente y trata de formular su destino colectivo en términos de “la condición cristiana”. El argumento central sostiene que la tragedia de la condición cristiana en el Medio Oriente se explica por la crisis del Estado secular provocada tanto por el factor del Islam, así como las intervenciones de potencias europeas desde las cruzadas hasta el período colonial e intervención militar de Estados Unidos en Irak en 2003. En este sentido, la actualidad no es la repetición de la historia, sino la continuidad del mismo padrón de inequidad en distintos períodos históricos dentro de las sociedades musulmanas y el intervencionismo externo/occidental que, tanto en el pasado como en la actualidad, muy pocas veces se ha preocupado por el destino de la cristiandad del Medio Oriente.

ALMG e Câmara se encontram para discutir gestão estratégica no legislativo

Notícia sobre o evento "Pensando o Novo Ciclo de Gestão Estratégica - Lições Aprendidas pela Assembleia Legislativa de Minas Gerais", promovido pela Assessoria de Projetos e Gestão - APROGE/DG da Câmara dos Deputados.

Projeto político-pedagógico para o Centro de Formação, Treinamento e Aperfeiçoamento da Câmara dos Deputados

Apresenta um estudo descritivo sobre os elementos e estratégias metodológicas para a elaboração de um Projeto Político-Pedagógico - PPP - para o Centro de Formação, Treinamento e Aperfeiçoamento da Câmara dos Deputados. Aborda aspectos teóricos, legais e conceituais relativos a um PPP numa instituição de ensino, mesmo que corporativa.

Mapeamento das competências existentes no quadro de gerentes básicos da Câmara dos Deputados : um estudo de caso

Identifica as competências gerenciais existentes no quadro de gerentes básicos da Câmara dos Deputados. Avalia em que grau tais gestores se sentem preparados para o exercício da função. Discute que lacunas podem existir no atual modelo de desenvolvimento gerencial da instituição.

O Parlamento Jovem e a experiência das escolas do legislativo mineiro e da Câmara dos Deputados : o desenvolvimento da cultura cívica, propícia à democracia

Aborda o Parlamento Jovem, importante programa para o desenvolvimento de uma cultura propícia à democracia e para a formação do jovem estudante. Avalia o impacto deste programa nos jovens, buscando identificar o grau de desenvolvimento de uma cultura política considerada importante para a qualidade da democracia. Compara o programa da Câmara dos Deputados com outros programas similares, como o desenvolvido pela Escola do Legislativo de Minas Gerais. Identifica limitações percebidas nos programas e sugere alternativas para que possa alcançar maior amplitude.

A gestão de pessoas nas Câmaras de Vereadores de municípios de até 50.000 habitantes

A expectativa de contribuir para o aprimoramento e o equilíbrio da democracia brasileira tem estimulado a Câmara dos Deputados a criar programas e projetos para promover a modernização dos órgãos legislativos estaduais e municipais. A fim de melhor direcionar as ações previstas e de identificar novas oportunidades de atuação, é necessário conhecer a situação administrativa atual das câmaras municipais, em especial no que diz respeito à gestão de pessoas. A observação cotidiana nos leva a supor que a infraestrutura administrativa existente nas câmaras de vereadores de municípios com população de até 50.0000 habitantes é inadequada e insuficiente para o pleno desempenho das atribuições institucionais dos parlamentares. O estudo propõe um projeto de pesquisa à Câmara dos Deputados para levantar dados que comprovem ou rejeitem a hipótese. São abordados princípios gerais da gestão de pessoas, segundo os critérios da Administração Pública e a nova visão gerencial apresentada pelo Plano Diretor de Reforma do Estado.