Literatura académica sobre el tema "Structure zonales"
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Artículos de revistas sobre el tema "Structure zonales"
López-Carbonell, M., A. Moret y M. Nadal. "Changes in Cell Ultrastructure and Zeatin Riboside Concentrations in Hedera helix, Pelargonium zonale, Prunus avium, and Rubus ulmifolius Leaves Infected by Fungi". Plant Disease 82, n.º 8 (agosto de 1998): 914–18. http://dx.doi.org/10.1094/pdis.1998.82.8.914.
Texto completoGerber, Edwin P. y Geoffrey K. Vallis. "A Stochastic Model for the Spatial Structure of Annular Patterns of Variability and the North Atlantic Oscillation". Journal of Climate 18, n.º 12 (15 de junio de 2005): 2102–18. http://dx.doi.org/10.1175/jcli3337.1.
Texto completoCash, Benjamin A., Paul J. Kushner y Geoffrey K. Vallis. "Zonal Asymmetries, Teleconnections, and Annular Patterns in a GCM". Journal of the Atmospheric Sciences 62, n.º 1 (1 de enero de 2005): 207–19. http://dx.doi.org/10.1175/jas-3361.1.
Texto completoHelfrich, Karl R. y Joseph Pedlosky. "Time-dependent isolated anomalies in zonal flows". Journal of Fluid Mechanics 251 (junio de 1993): 377–409. http://dx.doi.org/10.1017/s0022112093003453.
Texto completoWedi, Nils P. y Piotr K. Smolarkiewicz. "A Nonlinear Perspective on the Dynamics of the MJO: Idealized Large-Eddy Simulations". Journal of the Atmospheric Sciences 67, n.º 4 (1 de abril de 2010): 1202–17. http://dx.doi.org/10.1175/2009jas3160.1.
Texto completoSEVGİLİ, HASAN, DENİZ ŞİRİN, KLAUS-GERHARD HELLER y MİCHÈLE LEMONNIER-DARCEMONT. "Review of the Poecilimon (Poecilimon) zonatus species group and description of new species from Turkey with data on bioacoustics and morphology (Orthoptera: Phaneropterinae)". Zootaxa 4417, n.º 1 (3 de mayo de 2018): 1. http://dx.doi.org/10.11646/zootaxa.4417.1.1.
Texto completoHall, Nicholas M. J., George N. Kiladis y Chris D. Thorncroft. "Three-Dimensional Structure and Dynamics of African Easterly Waves. Part II: Dynamical Modes". Journal of the Atmospheric Sciences 63, n.º 9 (1 de septiembre de 2006): 2231–45. http://dx.doi.org/10.1175/jas3742.1.
Texto completoAdames, Ángel F. y John M. Wallace. "On the Tropical Atmospheric Signature of El Niño". Journal of the Atmospheric Sciences 74, n.º 6 (24 de mayo de 2017): 1923–39. http://dx.doi.org/10.1175/jas-d-16-0309.1.
Texto completoPilette, Daniel. "Les acteurs de zonage et leurs pratiques". Cahiers de géographie du Québec 22, n.º 57 (12 de abril de 2005): 393–420. http://dx.doi.org/10.7202/021411ar.
Texto completoMagnusdottir, Gudrun y Chia-Chi Wang. "Intertropical Convergence Zones during the Active Season in Daily Data". Journal of the Atmospheric Sciences 65, n.º 7 (1 de julio de 2008): 2425–36. http://dx.doi.org/10.1175/2007jas2518.1.
Texto completoTesis sobre el tema "Structure zonales"
Sama, Juvert Njeck. "The effect of beta on the nonlinear generation of zonal structures in experimentally relevant tokamak plasmas". Electronic Thesis or Diss., Université de Lorraine, 2024. https://docnum.univ-lorraine.fr/ulprive/DDOC_T_2024_0111_SAMA.pdf.
Texto completoSpatial gradients in temperature and density in tokamak plasmas excite micro-instabilities, which interact non-linearly to form turbulence. Turbulence increases heat and particle transport, reducing the energy confinement time. Understanding turbulence dynamics is important to achieving the conditions for self-sustained combustion in a fusion reactor. Zonal structures (ZS), i.e., the axisymmetric perturbations of a tokamak plasma, are generated by turbulence and play an important role in its self-consistent saturation. Two types of ZS exist: zero-frequency zonal flows (ZFZF) and geodesic acoustic modes (GAM). Recent electrostatic nonlinear studies of turbulence-excited GAMs in Asdex upgrade (AUG) have shown that radially extended GAM structures can be excited by turbulence. The dynamics of GAMs have recently been shown to change when going from low confinement mode (L-mode) to intermediate confinement mode (I-mode) and from I-mode to high confinement mode (H mode). In particular, GAMs are observed experimentally in L-mode and I-mode and are more rarely observed in H-mode. A first linear model explaining this behavior was constructed using the combination of their Landau and continuum damping, which affects GAMs more strongly in H mode. Zonal structures generated by the GAM modes can interact and couple with the zonal structures generated by the turbulence induced by the instabilities, such as the so-called ITG (Ion Temperature Gradient) type modes. Kinetic and particle trapping effects can oppose Landau damping and dominate the zonal flow dynamics generated by ITGs. It is particularly important to understand the dynamics of zonal flows, their excitation mechanism, and their interaction with different plasma instabilities and turbulence. In this thesis, the dynamics of GAMs and ZFZF are studied in different configurations. In Chapter Two, we study the linear dynamics of geodesic acoustic modes in anisotropic plasma. We studied the effects of ion temperature anisotropy that can be introduced by various plasma heating mechanisms, such as neutral beam injection (NBI), ion cyclotron resonance heating (ICRH), and electron cyclotron resonance heating (ECRH). We show that ion temperature anisotropy can significantly modify the damping rate of the geodesic acoustic mode. In the third chapter of this thesis, we developed a global linear theory to study the linear dynamics of plasma waves in tokamak geometry for arbitrary particle distribution functions. We report a generalized expression of the GAM frequency in terms of the distribution function of the ion species and the mode. The generalized mode structure equation of the Alfven/ITG mode structure equation is in the large poloidal mode number unit. In chapter four, the numerical simulation code ORB5 is discussed in detail, pointing out all assumptions and domains of applicability. In chapter five. Our main focus was investigating the impact of zonal flows forced-driven by Alfven modes on linear ITG instabilities. We isolated this effect from self-consistent nonlinear electromagnetic simulations and tested it independently using a set of numerical tools that will be discussed later. We show that zonal flows forced-driven by Alfven modes can significantly mitigate ITG instabilities in an experimentally relevant scenario magnetic geometry. In chapter six, we review the "particle mode" model. We show that the synchronization of particle modes leads to the amplification of the zonal flows, which occurs even when the ions and electrons admit to the same temperature
Uzawa, Ken. "Study of modulational instability and structure of zonal flows in fusion plasmas". Kyoto University, 2008. http://hdl.handle.net/2433/135587.
Texto completo0048
新制・課程博士
博士(エネルギー科学)
甲第13952号
エネ博第173号
新制||エネ||40(附属図書館)
UT51-2008-C868
京都大学大学院エネルギー科学研究科エネルギー基礎科学専攻
(主査)教授 岸本 泰明, 教授 近藤 克己, 教授 福山 淳
学位規則第4条第1項該当
Laage, de Meux Benoît de. "Modélisation des écoulements turbulents en rotation et en présence de transferts thermiques par approche hybride RANS/LES zonale". Chasseneuil-du-Poitou, Ecole nationale supérieure de mécanique et d'aérotechnique, 2012. https://theses.hal.science/docs/00/74/35/42/PDF/these_de_Laage.pdf.
Texto completoThe numerical simulation of turbulent flows in cooling system of hydrau- lic pumps sealing requires considering large computational domains and long integration times. The zonal hybrid RANS/LES modelling of turbulence could deal with such appli- cations, in order to reproduce the whole thermal and dynamical phenomena of the flow, with a computational cost compatible with industrial studies. This approach aims at pro- perly interfacing a Large Eddy Simulation (LES), which provides an accurate unsteady description of turbulence in some critical regions of the flow, with the statistical RANS approach, less demanding in computational resources, applied in the whole remaining fluid domain in order to take into account the imposed global variations of the flow (cool water injection in hot water, shaft and rotor rotation,. . . ). To this end, a detailed study of tur- bulence models appropriate for rotating flows is presented, following both the RANS and the LES approaches. Numerous turbulence models are compared in the rotating channel flow test case. The zonal coupling at boundary faces using the Synthetic Eddy Method (SEM) is studied and an innovative volumic coupling using a source term on overlapping RANS/LES area, the Anisotropic Linear Forcing, is proposed. For the first time, these two coupling methods are extended to heat transfer. The present zonal hybrid RANS/LES computations of static or rotating channel flows in isothermal or forced convection regimes, show the applicability of such modelling for industrial studies
FERREIRA, Débora Maria Cavalcanti. "Delimitação de espécie e filogeografia do complexo Cryptanthus zonatus (Vis.) Vis. (BROMELIACEAE)". Universidade Federal de Pernambuco, 2016. https://repositorio.ufpe.br/handle/123456789/18517.
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CAPES
Cryptanthus Otto & A.Dietr. (Bromeliaceae, Bromelioideae) é um gênero endêmico do Brasil. Cryptanthus burle-marxii Leme e C. zonatus (Vis.) Vis. são restritas ao norte da Floresta Atlântica nordestina e não apresentam delimitação taxonômica bem definida, pois muitos de seus caracteres morfológicos se sobrepõem. Ambas as espécies compõem o complexo C. zonatus (Vis.) Vis.. O objetivo do presente estudo foi realizar a delimitação de espécies e descrever os padrões filogeográficos do complexo C. zonatus, utilizando dados morfológicos, moleculares e de modelagem de nicho ecológico. Para o estudo foram feitos testes de amplificação heteróloga em C. burle-marxii e C. zonatus, utilizando 38 locos de microssatélites nucleares de cinco espécies de Bromeliaceae. Dos 38 locos testados, 24 apresentaram amplificação positiva e 13 foram polimórficos. Dez locos polimórficos foram selecionados para serem amplificados e genotipados em 147 indivíduos de oito populações do complexo C. zonatus. O resultado da análise morfológica e de estrutura genética mostrou que C. burle-marxii e C. zonatus são dois nomes dados à mesma espécie. A análise filogeográfica mostrou que a distribuição geográfica e estrutura genética do complexo C. zonatus pode ter sofrido modificações no quaternário. No último máximo glacial a distribuição geográfica potencial do complexo era contínua e maior em algumas áreas que atualmente é mar, o que deve ter ocorrido provavelmente devido à regressão marinha neste local. No Holoceno médio houve a potencial separação da distribuição possivelmente devido a uma barreira ecológica que perdurou até o presente formando dois grupos geneticamente estruturados, um ao norte e outro ao sul. Para a conservação da espécie foram indicadas populações prioritárias para o estabelecimento de unidades de conservação.
Cryptanthus Otto & A.Dietr. (Bromeliaceae, Bromelioideae) is an endemic genus from Brazil. Cryptanthus burle-marxii Leme and C. zonatus (Vis.) Vis. are species restricted to the north of the northeastern Atlantic Forest and have no well-defined taxonomic delimitation due to overlaping of some morphological characters. Both species are included in the Cryptanthus zonatus complex. The main goal of this study was to delimit species boudaries and to describe the phylogeographic patterns of the complex C. zonatus using morphological, molecular and ecological niche modeling data. For this study were carried out cross-amplification tests in C. burle-marxii and C. zonatus using 38 loci of nuclear microsatellite of five species of Bromeliaceae. Of the 38 loci tested, 24 showed positive amplification and 13 were polymorphic. Ten polymorphic loci were selected to be amplified and genotypes in 147 individuals from eight populations of the complex C. zonatus. The results of the morphological and genetic structure analyses showed that C. burle-marxii and C. zonatus are two names given to the same species. The phylogeographic analysis showed that the geographic distribution and genetic structure of the complex C. zonatus may have been modified in the Quaternary. The potential geographic distribution of the complex in the last glacial maximum was continuous and larger in some areas which are sea in present, what have probably occurred due to marine regression at this location. In the middle Holocene, there was the potential separation of distribution, possibly due to an ecological barrier that lasted until the present, forming two genetically structured groups, one in the north and other in the south. For conservation of the species priority populations were indicated for the establishment of protected areas
Galán, Fiestas Mary Isabel y Jaimes Marco Antonio Nieto. "Concreto de baja permeabilidad para pilotes prefabricados de muelles construidos en zonas de salpicaduras y mareas utilizando nanotubos de carbono de pared múltiple". Bachelor's thesis, Universidad Peruana de Ciencias Aplicadas (UPC), 2020. http://hdl.handle.net/10757/651959.
Texto completoDue to the importance of the maritime structures, it is required that the concrete with which they are manufactured guarantees their impermeability against the waters of the sea, being the piles of the docks those that suffer different anomalies when being in direct contact with the sulfates and chlorides, that progressively degrade it mainly causing its cracking. Carbon Nanotubes (NTC) have a large specific surface that affects the cement matrix by modifying hydrated calcium silicates, producing greater cohesion and consequently increasing the compactness of concrete. The present work seeks to reduce the permeability of the concrete of the prefabricated piles of the springs located in areas of splashes and tides, studying for it different physical and mechanical properties of the concrete with NTC; The results indicate that settlement decreases, compressive, tensile and flexural strengths increase and water penetration depth decreases.
Trabajo de investigación
Risbey, James S. (James Sydney). "An analysis of zonal mean atmospheric angular momentum and high cloud cover : periodicities, time-latitude structure, and cross correlations". Thesis, Massachusetts Institute of Technology, 1987. http://hdl.handle.net/1721.1/57727.
Texto completoFigueiredo, Gabriela Guerra Araújo Abrantes de. "Variação na estrutura trófica e no uso dos recursos alimentares da ictiofauna de zonas rasas ao longo de um gradiente estuarino-límnico". reponame:Repositório Institucional da FURG, 2014. http://repositorio.furg.br/handle/1/6114.
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O estudo da estrutura trófica de comunidades biológicas nos fornece uma descrição da organização e funcionamento do ecossistema e das interações entre as comunidades. Comparar a estrutura trófica das comunidades ao longo de gradientes ambientais pode fornecer novas interpretações em relação a sua organização trófica e serve de base para avaliar impactos antrópicos presentes e futuros. Um dos métodos mais comuns atualmente para se avaliar relações tróficas é a análise dos isótopos estáveis (AIE), o qual vem sendo utilizado para estimar os fluxos de matéria orgânica entre consumidores bem como sua posição trófica na cadeia alimentar. O objetivo principal dessa dissertação foi investigar a estrutura trófica da assembleia de peixes de zonas rasas ao longo de um gradiente estuarino–límnico, a partir da AIE de carbono (13C/12C) e nitrogênio (15N/14N) de fontes alimentares basais (i.e., plantas com fotossíntese C3 e C4 e matéria orgânica particulada em suspensão, POM) e peixes dominantes em cada sistema. Amostras de fontes alimentares basais, peixes e invertebrados foram coletados na primavera e verão entre 2009 e 2010 no estuário da Lagoa dos Patos, Canal São Gonçalo e Lagoa Mirim no extremo sul do Rio Grande do Sul. Biplots e métricas isotópicas (Convex hull e nicho isotópico) foram utilizadas para descrever e comparar a estrutura trófica da ictiofauna entre os ambientes. Análises de correlação foram realizadas para analisar a relação entre o comprimento total (CT) da ictiofauna e a posição trófica (PT). Modelos bayesianos de mistura isotópica foram empregados para avaliar a variabilidade no uso de recursos alimentares ao longo do gradiente ambiental para o barrigudinho Jenynsia multidentata, uma das únicas espécies frequentes ao longo de todo gradiente. A área total (Convex hull) e o nicho isotópico ocupado pela assembleia de peixes variaram marcadamente entre os ambientes, com o estuário apresentando uma área total duas vezes maior (CH: 50,28) do que o Canal e a Lagoa (17,51 e 20,29, respectivamente). Já o nicho isotópico, que é robusto aos efeitos de possíveis diferenças no número amostral, apresentou diferenças estatísticas entre estuário e os dois ambientes de água doce (p<0,00), porém esses dois últimos não apresentaram diferenças entre si (p>0,30). A AIE dos peixes no Canal sugere que a fragmentação de habitat ocasionada pela presença de uma barragem-eclusa afetou também a conectividade trófica entre o estuário da Lagoa dos Patos e Lagoa Mirim. Variações na razão isotópica do nitrogênio da comunidade também sugerem que impactos antrópicos como a eutrofização são mais acentuados no estuário da Lagoa dos Patos e Canal. As análises de correlações não mostraram correlação positiva entre o CT e PT. O modelo de mistura mostrou que as principais fontes alimentares basais para J. multidentata no canal foi POM, enquanto na lagoa foram principalmente plantas C4 e POM e no estuário houve uma maior sobreposição nos intervalos de credibilidade, não sendo possível distinguir diferenças significativas na contribuição relativa das fontes basais para a espécie. Nossos resultados mostraram que há diferenças na estrutura trófica e no uso de recursos alimentares ao longo do gradiente ambiental e que impactos antrópicos, como construção de barragem e eutrofização, afetam a ictiofauna nesses ambientes.
Trophic structure analyses of biological communities provide insights on ecosystem organization and functioning and also on communities’ interactions. Comparing the trophic structure of communities considering environmental gradients allows new interpretations of their trophic organization and evaluation of current and future anthropic impacts. One of the most common methods to evaluate trophic relationships is the stable isotope analysis (SIA), which has been used to estimate the flow of organic matter among consumers as well as its trophic position in the food chain. The main objective of this Master Thesis was to investigate the trophic structure of shallow areas fish assemblage along a freshwater-estuarine gradient, using the analysis of carbon (13C/12C) and nitrogen (15N/14N) isotope ratios of basal food sources (i.e., plants with C3 and C4 photosynthesis and particulate organic matter POM) and dominant fishes in each system. Basal food sources, fishes and invertebrates were collected at Lagoa dos Patos estuary, São Gonçalo Channel and Lagoa Mirim, located in the southern most in Brazil, during spring and summer seasons of 2009 and 2010. Biplots and isotopic metrics (Convex hull and isotopic niche) were used to describe and compare the trophic structure obtained in the three environments. Correlation analyzes were conducted to examine the relationship between total length (TL) of the ichthyofauna and trophic position (TP). Bayesian models of isotopic mixing were used to evaluate the variability in food resource use by the one-sided livebearer Jenynsia multidentata along the environmental gradient, which was one of the only species found along the entire gradient. The total area (Convex hull) and the isotopic niche occupied by the fish assemblage showed an marked variation among environments. The Convex hull total area of the estuary (CH: 50.28) was two-fold higher than the Channel and Lagoa Mirim areas (17,51 and 20.29, respectively). The isotopic niche, which is not affected by differences in sample sizes, showed statistical differences between the estuary and the two freshwater systems ( (p<0.00), but there were no statistical differences when the freshwater systems were compared with each other (p>0.30). The SIA analysis of fishes in the Channel suggests that the habitat fragmentation caused by a dam also affected the trophic connectivity between the Lagoa dos Patos estuary and the Lagoa Mirim. Comparison of the nitrogen isotope ratio values among communities also suggested that anthropogenic impacts (e.g., eutrophication) were more evident in the Lagoa dos Patos estuary and Channel. The analysis of correlations didn't show any positive correlation between TL and TP. The mixing model showed that the main basal food sources sustaining J. multidentata in the Channel was POM, whereas in the Lagoa Mirim was mainly C4 plants and POM. Moreover, in the estuary, it was found a greater overlap on the credibility intervals of basal food sources and it was not possible to distinguish statistical differences between their relative contributions to the specie. Our results showed that there are differences on the trophic structure and on the use of food resources along the environmental gradient. Also, anthropogenic impacts, such as dam constructions and eutrophication, have an affect on the ichthyofauna of these environments.
Fujisaki, Érica Tieko. "Produção primária e estrutura da comunidade fitoplanctônica nas zonas limnética e litorânea da represa Álvaro de Souza Lima (Bariri, SP) em quatro épocas do ano". Universidade de São Paulo, 2001. http://www.teses.usp.br/teses/disponiveis/18/18139/tde-25012017-160020/.
Texto completoTemporal and spacial variations of phytoplankton primary production in Bariri Reservoir (22º06\'S and 48º45\'W, São Paulo State, Brazil) were evaluated by in situ observations in two different areas: one in the limnetic zone (M1) and other in the littoral zone (M2) in February, April, July and September 1998. The phytoplankton primary productivity was determined by the dissolved oxigen method. The values of net primary productivity of the phytoplankton community in M1 varied from 122 mgO2.m-2.h-1 (April) to 2093 mgO2.m-2.h-1 (July), and M2, varied from 157 (April) to 861 mgO2.m-2.h-1 (February). The community respiration M1, varied from 18 (April) to 376 mgO2.m-2.h-1 (February) and M2, varied from zero (April) to 211 mgO2.m-2.h-1 (February).The lowest primary productivity, obtained in April, coincided with the lowest biomass. Probably, phosphorus was the main limitation of the primary productivity on the others study months. The bloom of Microcystis spp (S strategist) in February M1 and M2 and July M1 was related to water column more stable in these periods. In July M1, April M1 and M2 and September M1 and M2, the R and C strategists predominated, such as Rhodomonas lacustri, Aulacoseira granulata granulata, Chlamydomonas spp, Cryptomonas brasiliensis, Cryptomonas tetrapyrenoidosa, Anabaena spiroides and Anabaena circinalis.
Miranda, Alan Wanderley Albuquerque. "Evolução estrutural das zonas de cisalhamento dúcteis na porção centro-leste do domínio da Zona Transversal na Província Borborema". Universidade do Estado do Rio de Janeiro, 2010. http://www.bdtd.uerj.br/tde_busca/arquivo.php?codArquivo=2912.
Texto completoThe studied area is inserted in the Transversal Domain of Borborema Province. The Paleoproterozoic (Riacian) basement encompasses mainly by metaplutonic rocks from Salgadinho and Cabaceiras Complex. These complexes were individualized according to their compositional, textural and/or geochronological datas. The Paleoproterozoic (Orosirian) metasedimentary rocks were interpreted as components of Sertânia Complex. The Estatherian magmatic event is characterized by syenogranitic orthogneisses of the Carnoió-Caturité Suite and metaplutonic rocks of Metanorthositic Boqueirão Complex. The Neoproterozoic lithostratigraphic units are represented by Cryogenian metasedimentary successions of Complex Surubim and by Early-Ediacaran granodioritic and syenogranitic orthogneisses and of the Sumé Complex and Riacho de Santo Antonio orthogneisses, respectively. The Ediacaran granitic magmatism was characterized by the emplacement of Inácio Pereira and Marinho Plutons. The geochronological data (LA-ICPMS) indicate at least of three tectono-magmatic events. The 2042 + 13Ma and 1996 + 11Ma ages from amphibolites of Cabaceiras Complex were interpreted as the crystallization age of the protolith and metamorphism, respectively. The age of 1638 + 13Ma from the syenogranitic hornblende orthogneiss of Carnoió-Caturité Suite was interpreted as the crystallization age of the protolith, marking an Estatherian anorogenic magmatic event. The age of 550 + 3.1Ma acquired in a porphyritic monzogranite of Marinho Pluton is a record of the last magmatic event in the Late-Ediacaran, associated with the final stage of development of the Coxixola Shear Zone. The structural data allowed the individualization of three deformation phases, individualized as D1, D2 and D3. D1 was responsible for generating a S1 foliation, observed only at the hinge of F2 folds. The D2 event is marked by a thrust regime with transport to NNW, observed from asymmetrical shear bands and drag folds in sections parallel to stretching lineation (L2x). Ductile shear zones of different geometry and kinematics had been developed during the D3 phase. The NE-SW Boa Vista, Carnoió and Congo Shear zones exhibit sinistral kinematic in sections parallel to stretching lineation (L3x). The southern limits of these shear zones are connected with Coxixola Shear Zone. This WSW-ENE shear zone with dextral kinematics crosscut the entire studied area, with an average of 300m thickness of mylonitic rocks. The WNW-ESE Inácio Pereira Shear Zone is situated in the eastern portion of the studied area, shows geometric and kinematic characteristics in agreement with an evolution through an oblique-sinistral transpressive regime. The structural evolution of a system of conjugate ductile shear zones is responsible by anastomosed framework exposed in a map view.
Neves, Leonardo Mitrano. "Fatores estruturadores das assembl?ias de peixes em tr?s distintas zonas (rio, mistura e costeira) do estu?rio do rio Mambucaba, Angra dos Reis- RJ". Universidade Federal Rural do Rio de Janeiro, 2009. https://tede.ufrrj.br/jspui/handle/jspui/1207.
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Conselho Nacional de Desenvolvimento Cient?fico e Tecnol?gico - CNPQ
The estuarine systems influence fish assemblages, throughout their longitudinal gradients and remarkable salinity changes. Such assemblages adapt to different habitat constraints and change in spatial and temporal scales. The aim of this study was to assess the ichthyofauna composition and structure in three zones of the Mambucaba estuary (CZ ? coastal zone; MZ ? mixture zone and RZ ? river zone) and their relationship with environmental variables and habitat characteristics. Systematic fish collections (2 months in each seasons) were performed between October 2007 and August 2008, by using otter trawl at two sites in CZ (C1 e C2), beach seine at three sites in MZ (M1, M2, M3) and mesh trays at two sites in RZ (R1 e R2). At each fish sampling occasion, both surface and depth environmental variables of temperature, salinity, conductivity, turbidity and dissolved oxygen were taken and depth was measured. A total of 14,320 individuals, in 111 species (RZ ? 18; MZ ? 50, and CZ - 66) were collected. Distinct fish assemblages were found for each zone, as indicated by low number of common species (14 - MZ and CZ; 8 - MZ and RZ; and 2 - CZ and RZ), and only one abundant species (> 1% of the total number of fish within the zone) being common in more than one zone (Eucinostomus argenteus in CZ and MZ). Such pattern can be related to high salinity variation in MZ and narrow (20 m) channel width connecting the estuary with the sea, which can limit fish movement (into/out of the estuary). In CZ, the three more abundant species were Paralonchurus brasiliensis, Ctenosciaena gracillicirrhus, Anchoa lyolepis, Larimus breviceps and Stellifer brasiliensis, with large contribution of fish from the Scieanidae family in this zone (18 species). Spatial changes inf fish species were not consistent in CZ, probably due to lack of spatio-temporal estuarine plume influence on depth environmental variables (ANOVA, p>0.05). Depth was the main factor to influence spatial changes for Diapterus rhombeus (negative association) more abundant in C1 (average depth = 10 m; ANOVA, p<0.05) and Micropogonias furnieri, P. brasiliensis and Pellona harroweri (positive association) more abundant in C2 (average depth = 17 m; ANOVA, p<0.00). Diapterus rhombeus and Etropus crossotus occured mainly in Spring and Summer, and Eucinosomus gula in Spring. The most abundant species in CZ, typical of high salinty influence, is a indication that this zone have characteristics to inner continental shelf. In MZ, most abundant species (Eugerres brasilianus, Eucinostomus melanopterus, Trinectes paulistanus, Gobionellus shufeldti, G. oceanicus, Geophagus brasiliensis, Centropomus parallelus and Citharichthys arenaceus) have higher number and weight of individuals in M1 (ANOVA, p<0.01), an adjacent lagoon connected to the main channel. In spite of the significant negative correlation between this species and salinity (r-Spearman>0.32, p<0.01), the more sheltered areas in M1 seem to be more important to determine this pattern than salinity itself. The site M1 also have more number of individuals and species (ANOVA, p<0.01), and larger number of fish of smaller size (CT median = 58mm) compared to M2 and M3, located in the main channel (median = 106mm) according to Median and Kruskall-Wallis tests (p<0.01; 2 = 1167.5), indicating the importance of this area for species recruitment. Low average similarity (SIMPER) for sites M2 (38.7%) and M3 (17.8%) indicate larger variability of assemblage in these sites, probably due to lesser habitat structure e higher dynamism. In RZ, the fish assemblage have few species (5) with abundance higher than 1% of the total number of fishes, being dominated by Dormitator maculatus, Astyanax sp and ix Microphis brachyurus lineatus, species typical of upper estuaries and lower river reaches. Spatial variation was detected for D. maculatus only, more abundant at R2, a site with abundant riparian vegetation, mainly grass. Dormitator maculatus was more abundant in Summer and Autumn, M. brachyurus lineatus, in Spring, Autumn and Winter and Astyanax sp was absent in Spring only. Patterns in fish assemblage structure were at large scale, primarily species-specific responses to dominant environmental gradient, while at small scale, results of association with the habitat.
Os sistemas estuarinos influenciam as assembl?ias de peixes, ao longo de seus gradientes longitudinais e das marcadas varia??es da salinidade. Estas assembl?ias se adaptam ?s diferentes condicionantes do habitat e variam em escalas espaciais e temporais. O objetivo do presente estudo foi avaliar a composi??o e estrutura da ictiofauna em tr?s zonas do estu?rio do rio Mambucaba (ZC ? zona costeira; ZM ? zona de mistura e ZR ? zona de rio) e suas rela??es com as vari?veis ambientais e caracter?sticas do habitat destas zonas. Coletas sistem?ticas de peixes (2 meses por esta??o do ano) foram realizadas entre outubro de 2007 e agosto de 2008, com arrastos de fundo em dois locais da ZC (C1 e C2), arrasto de praia em 3 locais da ZM (M1, M2, M3) e peneira em 2 locais da ZR (R1 e R2). Em cada amostragem de peixes, foram tomadas, para a superf?cie e fundo, as vari?veis ambientais de temperatura, salinidade, condutividade, turbidez e oxig?nio dissolvido, bem como medida a profundidade. Um total de 14320 indiv?duos, constitu?dos por 111 esp?cies (ZR ? 18; ZM ? 50 e ZC - 66) foram coletados. Assembl?ias de peixes distintas foram identificadas para cada zona, indicadas pelo baixo n?mero de esp?cies comuns (14 - ZM e ZC; 8 - ZM e ZR; e 2 - ZC e ZR), e com apenas uma esp?cie abundante (> 1% do numero total de peixes na zona) comum em mais de uma zona (Eucinostomus argenteus na ZC e ZM). Tal padr?o pode estar relacionado ? maior variabilidade da salinidade existente na ZM e a estreita (20 m) largura do canal de conex?o com o mar, fatores que podem ser limitantes aos movimentos (entrada/sa?da) de peixes. Na ZC, as tr?s esp?cies mais abundantes foram Paralonchurus brasiliensis, Ctenosciaena gracillicirrhus, Anchoa lyolepis, Larimus breviceps e Stellifer brasiliensis, com a maior participa??o de peixes da fam?lia Sciaenidae nesta zona (18 esp?cies). As varia??es espaciais das esp?cies foram pouco consistentes na ZC, provavelmente relacionado a influencia da pluma estuarina n?o ter provocado mudan?as espa?o-temporais nas vari?veis ambientais de fundo (ANOVA, p>0,05). A profundidade foi o principal fator respons?vel pela separa??o espacial encontrada para Diapterus rhombeus (associa??es negativas) mais abundante em C1 (profundidade m?dia = 10 m; ANOVA, p<0,05) e Micropogonias furnieri, P. brasiliensis e Pellona harroweri (associa??es positivas) mais abundantes em C2 (profundidade m?dia = 17 m; ANOVA, p<0,00). Diapterus rhombeus e Etropus crossotus ocorreram principalmente na primavera e ver?o, e Eucinosomus gula na primavera. As esp?cies mais abundantes da ZC, t?picas de ?guas com maior influencia salina, ? um indicativo de que esta zona tem caracter?sticas mais associadas ? plataforma continental interna. Na ZM, a maioria das esp?cies mais abundantes (Eugerres brasilianus, Eucinostomus melanopterus, Trinectes paulistanus, Gobionellus shufeldti, G. oceanicus, Geophagus brasiliensis, Centropomus parallelus e Citharichthys arenaceus) apresentou maior n?mero e peso de indiv?duos em M1 (ANOVA, p<0,01), uma lagoa adjacente conectada ao canal principal. Apesar das correla??es negativas significativas observadas entre estas esp?cies e a salinidade (r-Spearman>0.32, p<0,01), as ?reas mais abrigadas em M1 parecem ser mais determinantes neste padr?o do que a salinidade em si. O local M1 tamb?m apresentou o maior n?mero de indiv?duos e de esp?cies (ANOVA, p<0,01), com maior n?mero de peixes de menor tamanho (CT mediana = 58mm) do que dos locais M2 e M3, situados no canal principal (mediana = 106mm) de acordo com o Teste das Medianas e Teste de Kruskallvii Wallis (p<0,01; 2 = 1167,5), indicando a import?ncia desta ?rea para o recrutamento das esp?cies. A baixa similaridade m?dia (SIMPER) para os locais M2 (38,7%) e M3 (17,8%) indicam uma maior variabilidade na assembl?ia destes locais, possivelmente devido a menor estrutura??o do habitat e maior dinamismo. Na ZR, a assembl?ia de peixes apresentou poucas esp?cies (5) com abund?ncia maior que 1% do n?mero total de peixes, sendo dominada por Dormitator maculatus, Astyanax sp e Microphis brachyurus lineatus, esp?cies t?picas de ?reas lim?trofes entre a zona superior do estu?rio e a zona baixa de rio. Varia??es espaciais foram detectadas apenas para D. maculatus, mais abundantes em R2, um local com abundante vegeta??o marginal composta principalmente por gram?neas. D. maculatus foi mais abundante no ver?o e outono, M. brachyurus lineatus, na primavera, outono e inverno e Astyanax sp foi ausente somente na primavera. Os padr?es na estrutura da assembl?ia de peixes s?o, em maior escala, primariamente resultado das respostas individuais das esp?cies ao gradiente ambiental dominante, enquanto em menor escala, resultado das associa??es com o habitat.
Libros sobre el tema "Structure zonales"
Coloquio de Historia y Medio Físico. (1st 1989 Almería, Spain). El agua en zonas áridas, arqueología e historia: Actas del I Coloquio de Historia y Medio Físico, Almería, 14-15-16 de diciembre de 1989. [Almería]: Instituto de Estudios Almerienses de la Diputación de Almería, 1989.
Buscar texto completoPlatov, Nikolay. Fundamentals of engineering Geology. ru: INFRA-M Academic Publishing LLC., 2021. http://dx.doi.org/10.12737/1091050.
Texto completoGruzdev, Vladimir, Sergey Suslov, Vladimir Kosinskiy y Mariya Hrustaleva. Changes in the composition and structure of the components of the landscapes of the forest zone in the conditions of technogenesis. ru: INFRA-M Academic Publishing LLC., 2023. http://dx.doi.org/10.12737/1850657.
Texto completoEl agua en zonas aridas, arqueologia e historia: Actas del I Coloquio de Historia y Medio Fisico, Almeria, 14-15-16 de diciembre de 1989 (Coleccion Actas). Instituto de Estudios Almerienses de la Diputacion de Almeria, 1989.
Buscar texto completoCommon High Performance Computing Software Support Initiative (CHSSI) computational Fluid Dynamics (CFD)-6 Project. ARL Block-Structured Gridding Zonal Navier-Stokes Flow (ZNSFLOW) Solver Soft. Storming Media, 2000.
Buscar texto completoTibaldi, Stefano y Franco Molteni. Atmospheric Blocking in Observation and Models. Oxford University Press, 2018. http://dx.doi.org/10.1093/acrefore/9780190228620.013.611.
Texto completoGoswami, B. N. y Soumi Chakravorty. Dynamics of the Indian Summer Monsoon Climate. Oxford University Press, 2017. http://dx.doi.org/10.1093/acrefore/9780190228620.013.613.
Texto completoCapítulos de libros sobre el tema "Structure zonales"
Prasad, Sarvamangala V., Gautam Kaul y Bonnie S. Dunbar. "Structure and Function of Mammalian Zonae Pellucidae". En Introduction to Mammalian Reproduction, 203–25. Boston, MA: Springer US, 2003. http://dx.doi.org/10.1007/978-1-4615-0273-9_12.
Texto completoDunbar, Bonnie S., S. V. Prasad y T. M. Timmons. "Comparative Structure and Function of Mammalian Zonae Pellucidae". En A Comparative Overview of Mammalian Fertilization, 97–114. Boston, MA: Springer US, 1991. http://dx.doi.org/10.1007/978-1-4757-8982-9_6.
Texto completoLiu, Luo-Qin. "Far-Field Asymptotics and Zonal Structure of Theoretical Flow Models". En Unified Theoretical Foundations of Lift and Drag in Viscous and Compressible External Flows, 29–58. Singapore: Springer Singapore, 2017. http://dx.doi.org/10.1007/978-981-10-6223-0_2.
Texto completoSimpson, John I., Johannes Van der Steen y Joep Tan. "Eye Movements and the Zonal Structure of the Rabbit Flocculus". En The Cerebellum Revisited, 255–66. New York, NY: Springer US, 1992. http://dx.doi.org/10.1007/978-1-4612-2840-0_13.
Texto completoScott, R. K. "The structure of zonal jets in shallow water turbulence on the sphere". En IUTAM Symposium on Turbulence in the Atmosphere and Oceans, 243–52. Dordrecht: Springer Netherlands, 2010. http://dx.doi.org/10.1007/978-94-007-0360-5_20.
Texto completoFung, J. C. H., J. C. R. Hunt, R. J. Perkins, A. A. Wray y D. Stretch. "Defining the Zonal Structure of Turbulence Using the Pressure and Invariants of the Deformation Tensor". En Advances in Turbulence 3, 395–404. Berlin, Heidelberg: Springer Berlin Heidelberg, 1991. http://dx.doi.org/10.1007/978-3-642-84399-0_43.
Texto completoShagalov, S. V. y G. V. Rybushkina. "Nonlinear Development of Unstable Modes and Formation of Coherent Vortex Structures in Weakly Supercritical Zonal Shear Flows". En Progress in Turbulence V, 189–94. Cham: Springer International Publishing, 2014. http://dx.doi.org/10.1007/978-3-319-01860-7_30.
Texto completoBakas, Nikolaos A. y Petros J. Ioannou. "Emergence of Nonzonal Coherent Structures". En Zonal Jets, 419–34. Cambridge University Press, 2019. http://dx.doi.org/10.1017/9781107358225.027.
Texto completoKampianaki, Theofili. "Zonaras’ Working Method and Treatment of His Sources". En John Zonaras' Epitome of Histories, 38—C3.P58. Oxford University PressOxford, 2022. http://dx.doi.org/10.1093/oso/9780192865106.003.0004.
Texto completoWang, Z. J. "Conservative Interface Algorithm for Overlapped Structured/Structured, Structured/Unstructured Grids". En Numerical Methods for Fluid Dynamics V, 253–62. Oxford University PressOxford, 1996. http://dx.doi.org/10.1093/oso/9780198514800.003.0017.
Texto completoActas de conferencias sobre el tema "Structure zonales"
Jiaying, Wang, Lu Chunguang, Deng Lan y Xie Danyu. "Research on Intelligent Interactive Regulation Framework Based on Hierarchical and Zonal Structure Supporting Large-scale New Adjustable Load Resources". En 2024 China International Conference on Electricity Distribution (CICED), 793–801. IEEE, 2024. http://dx.doi.org/10.1109/ciced63421.2024.10753935.
Texto completoAnderson, Johan, Eun-jin Kim, Olivier Sauter, Xavier Garbet y Elio Sindoni. "Model of intermittent zonal flow structure formation". En THEORY OF FUSION PLASMAS. AIP, 2008. http://dx.doi.org/10.1063/1.3033708.
Texto completoMakarov, Vladimir, Ludmila Ksendzenko, Nicolai Opanasiuk y Andrei Golosov. "Zonal failure structure near the deep openings". En Eighth International Conference on Deep and High Stress Mining. Australian Centre for Geomechanics, Perth, 2017. http://dx.doi.org/10.36487/acg_rep/1704_30_makarov.
Texto completoJovanović, D., P. K. Shukla, Bengt Eliasson y Padma K. Shukla. "Structures and Zonal Flows in Magnetized Plasmas". En NEW FRONTIERS IN ADVANCED PLASMA PHYSICS. AIP, 2010. http://dx.doi.org/10.1063/1.3533182.
Texto completoYang, Hong, Dirk Nuernberger y Hans-Peter Kersken. "Towards Excellence in Turbomachinery CFD: A Hybrid Structured-Unstructured RANS Solver". En ASME Turbo Expo 2005: Power for Land, Sea, and Air. ASMEDC, 2005. http://dx.doi.org/10.1115/gt2005-68735.
Texto completoCheverez-Gonzalez, Daniel y Christopher L. DeMarco. "Laplacian Structure in Power Network Constraints and Inherent Zonal Price Regions". En 2006 38th North American Power Symposium. IEEE, 2006. http://dx.doi.org/10.1109/naps.2006.359589.
Texto completoHEFAZI, H. y L. CHEN. "An Euler zonal method using composite structured and unstructured meshes". En Flight Simulation Technologies Conference and Exhibit. Reston, Virigina: American Institute of Aeronautics and Astronautics, 1990. http://dx.doi.org/10.2514/6.1990-3050.
Texto completoRotaru, Vasile K., Igor V. Dementiev, Oleg Y. Korshak, Sevastian Neamtsu, Stephan V. Robu, Hossin A. Abdeldayem, Igor V. Ciapurin y Nickolai V. Kukhtarev. "Photothermoplastic films as recorders in observation systems of zonal structures". En Defense and Security, editado por Robert D. Habbit, Jr. y Peter Tchoryk, Jr. SPIE, 2004. http://dx.doi.org/10.1117/12.543759.
Texto completoDEWAR, ROBERT L. y R. F. ABDULLATIF. "ZONAL FLOW GENERATION BY MODULATIONAL INSTABILITY". En Proceedings of the COSNet/CSIRO Workshop on Turbulence and Coherent Structures in Fluids, Plasmas and Nonlinear Media. WORLD SCIENTIFIC, 2007. http://dx.doi.org/10.1142/9789812771025_0017.
Texto completoKrommes, John A., A. Sen, S. Sharma y P. N. Guzdar. "Advances and Current Challenges in the Theory of Zonal-Flow Generation". En INTERNATIONAL SYMPOSIUM ON WAVES, COHERENT STRUCTURES AND TURBULENCE IN PLASMAS. AIP, 2010. http://dx.doi.org/10.1063/1.3526158.
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