982 resultados para Cross-correlation
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Magdeburg, Univ., Fak. für Naturwiss., Diss., 2010
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Magdeburg, Univ., Fak. für Humanwiss., Diss., 2013
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Magdeburg, Univ., Fak. für Naturwiss., Diss., 2014
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Otto-von Guericke-Universität Magdeburg, Fakultät für Naturwissenschaften, Dissertation, 2016
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v.17:no.1(1927)
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Foi realizado um levantamento em 41 áreas de um solo classificado como Latossol Vermelho Amarelo, com amostragens de solo e de folhas da forrageira "Coast Cross nº 1" objetivando o estudo de correlações entre as concentrações de nutrientes, alumínio e sódio nas folhas e as análises físicas do solo. Os autores observaram que a concentração de potássio nas folhas correlaciona-se negativamente com a fração silte do solo. A concentração de cobre nas folhas correlaciona-se negativamente com a fração areia fina e positivamente com argila. Ferro, manganês, zinco, sódio, boro e alumínio não apresentam correlações entre as suas concentrações foliares e os teores de argila no solo.
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Foi realizado um levantamento em 41 pontos de um Latossolo Vermelho Amarelo, com amostragem de solo e folhas da forrageira "Coast Cross Nº 1", objetivando o estudo de correlações entre as concentrações de nutrientes, alumínio e sódio nas folhas e as análises químicas do solo. As folhas foram secas e analisadas para N, P. As amostras de solo foram secas e analisadas pelos seguintes métodos: índices pH (água e CaCl2 0,01 M), matéria orgânica (digestão úmida) , P, K, B, Cu, Fe, Mn, Zn e Na pelo extrator de Mehlich. P através de resina iônica. Ca, Mg e Al pelo KC1 1 N. As frações granulométricas foram dispersas por NaOH 0,1 Ne separadas pelo método da pipeta. Foram observadas correlações entre as concentrações de elementos nas folhas e as determinações no solo. Nitrogênio nas folhas correlacionou-se negativamente com fósforo do solo e positivamente com manganês e enxofre. Fósforo nas folhas correlacionou-se negativamente com cálcio do solo.
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Here we examine major anatomical characteristics of Corydoras aff. paleatus (Jenyns, 1842) post-hatching development, in parallel with its neurobehavioral evolution. Eleutheroembryonic phase, 4.3-8.8 days post-fertilization (dpf); 4.3-6.4 mm standard length (SL) encompasses from hatching to transition to exogenous feeding. Protopterygiolarval phase (8.9-10.9 dpf; 6.5-6.7 mm SL) goes from feeding transition to the commencement of unpaired fin differentiation, which marks the start of pterygiolarval phase (11-33 dpf; 6.8-10.7 mm SL) defined by appearance of lepidotrichia in the dorsal part of the median finfold. This phase ends with the full detachment and differentiation of unpaired fins, events signaling the commencement of the juvenile period (34-60 dpf; 10.8-18.0 mm SL). Eleutheroembryonic phase focuses on hiding and differentiation of mechanosensory, chemosensory and central neural systems, crucial for supplying the larval period with efficient escape and nutrient detection-capture neurocircuits. Protopterygiolarval priorities include visual development and respiratory, digestive and hydrodynamic efficiencies. Pterygiolarval priorities change towards higher swimming efficacy, including carangiform and vertical swimming, necessary for the high social interaction typical of this species. At the end of the protopterygiolarval phase, simple resting and foraging aggregations are seen. Resting and foraging shoals grow in complexity and participant number during pterygiolarval phase, but particularly during juvenile period.
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The severely poor are very poor since their consumption is far below the absolute poverty line, and the chronically poor are very poor since their consumption persists for long periods below the absolute poverty line. A combination of chronic poverty and severe poverty (CSP) must represent the very worst instance of poverty. Yet the exercise in this paper of asking simple questions about CSP shows large research gaps. Quantified statements on CSP at the country level can be made for just 14 countries, and at the household level in just six countries. This data suggests a positive correlation between severe poverty and chronic poverty, both at the country level and the household level. Understanding the CSP relationship whether it is strong, where it arises, what causes it may improve our explanation of observed cross-country variation in the elasticity between macroeconomic growth and poverty reduction, and why within countries, some households take better advantage of opportunities afforded by macroeconomic growth. Some limited data suggests similarity in socioeconomic characteristics of the severe poor and the chronic poor in terms of location, household size, gender, education and economic sector of work. Of concern is that microlongitudinal datasets drop large proportions of their base year samples, and how this affects our understanding of CSP is not well evaluated. On causal mechanisms, evidence suggests that CSP may be caused by parental CSP (i.e. an intergenerational CSP cycle) and in households not previously poor, CSP may be caused by a morbidity cycle.
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Feces of 34 dogs out of 251 (13.5%) from guanabara were positive for Isospora. From these 19 (7.5%) were i. rivolta, 13 (5.2%) were I. canis and 2 (0,7) were i. bigemina. "Free-sporocysts" of I. rivolta were eliminated by 9 dogs (3.5%). A "Caryospora-like" oocyst was seen once. Cross-infection experiments performed with Isospora from dogs and cats failed to produce infection while inoculations of these Isospora in their natural hosts succeeded. The results suggest that the species of Isospora occurring in cats are different from those of dogs.
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Adult normal inbred mice rendered tolerant to OVA by previous oral exposure do not respond to intraperitonela immunization with DNP-OVA in adjuvant. These tolerant mice also form less DNP-specific antibodies to DNP-KLH when immunized with mixtures of DNP-KLH and DNP-OVA, or less HGG-specific antibodies when immunized with cross-linked conjugates of OVA and HGG. These same procedures increased DNP-specific or HGG-specific responses in non-tolerant control mice. The cross-supperssion was ineffective, however, to inhibit already ongoing antibody responses.
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Contribució al Seminari: "Les Euroregions: Experiències i aprenatges per a l’Euroregió Pirineus-Mediterrània", 15-16 de desembre de 2005
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Contribució al Seminari: "Les Euroregions: Experiències i aprenatges per a l’Euroregió Pirineus-Mediterrània", 15-16 de desembre de 2005
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There is recent interest in the generalization of classical factor models in which the idiosyncratic factors are assumed to be orthogonal and there are identification restrictions on cross-sectional and time dimensions. In this study, we describe and implement a Bayesian approach to generalized factor models. A flexible framework is developed to determine the variations attributed to common and idiosyncratic factors. We also propose a unique methodology to select the (generalized) factor model that best fits a given set of data. Applying the proposed methodology to the simulated data and the foreign exchange rate data, we provide a comparative analysis between the classical and generalized factor models. We find that when there is a shift from classical to generalized, there are significant changes in the estimates of the structures of the covariance and correlation matrices while there are less dramatic changes in the estimates of the factor loadings and the variation attributed to common factors.