1000 resultados para Teorema do indice
Resumo:
Indices globais pulicidianos, anoplurianos, malofagianos e acarianos foram determinados em mamiferos capturados na Ilha de Manacá, Roraima, Brasil, no periodo de, novembro de 1987 a fevereiro de 1989.Tendo-se em vista os valores limites ou criticas atri-buidos aos indices pulicidianos, propostos como medida complementar de vigilância epide-miológica para peste, alguns, roedores silvestres poderiam ter estado expostos a esta in-fecção. O indice global foi de 11,5e a pulga prevalente foi Polygznis klagesi klagesiobservado na estação seca. Os números máximos de ectoparasitas por hospedeiros foram: 244 para Prorchimys guyannensis, 193para Prorchimyssp. e 108 para Bolomys sp. As espéciescom indices de infestação mais elevados fonam P. klagesi klagesiem Peoechimyssp.; Glíricolasp. n., Tur apicalise Tur aymaraem P. guyannensis.infestações simples foram de mais prevalentes, enquanto as duplas e as outras múltiplas foram equivalentes. Com exceção deProechimyssp., todas as espécies de hospedeiros apresentaram infestações simples. Apenas Laelaps dearmasie Gliricola porcelliocorreram em infestações iso-ladas.
Resumo:
In this work, an empirical system was developed to obtain a quality index for rock slopes in road infrastructures, named Slope Quality Index (SQI), and it was applied to a set of real slopes. The SQI is supported in nine factors affecting slope stability that contemplate the evaluation of different parameters. Consequently, each factor is classified by degree of importance and influence by assigned weights. These weights were established through a statistical analysis of replies to a survey that was distributed to several experienced professionals in the field. The proposed SQI varies between 1 and 5, corresponding to slopes in very good and very bad condition state, respectively. Besides the advantage linked to a quantitative and qualitative evaluation of slopes, the SQI also allows identifying the most critical factors on the slope stability, which is a fundamental issue for an efficient management of the slope network in the road infrastructure, namely in the planning of conservation and maintenance operations.
Resumo:
El presente proyecto consta de dos partes. 1. Modelos exponenciales con dispersión. 2. Ajuste de modelos lineales generalizados para datos de conteo con superdispersión. (...) Objetivos generales y específicos: El estudio de los modelos exponenciales con dispersión conduce a desarrollar y perfeccionar métodos de estimación y de inferencia tanto desde el punto de vista teórico como numérico. (...) i) Presentar, sin sin usar el teorema de Mora, resultados sobre la convergencia de modelos exponenciales con dispersión infinitamente divisibles. ii) Proponer una metodología apropiada para el análisis estadístico de variables aleatorias discretas enteras en función de posibles modelos adoptados para su explicación. Construcción de los algoritmos necesarios para la estimación de los parámetros especificados en el modelo adoptado y presentación de las macros correspondientes para su implementación.
Resumo:
Se estudiará la geometría de subvariedades haciendo hincapié en los grupos de holonomia de la conexión normal, herramienta que ha sido muy útil para atacar diversos problemas clásicos. Se estudiarán los siguientes problemas concretos: a) Resolver la conjetura de que toda subvariedad homogénea irreducible y substancial de la esfera cuyo grupo de holonomia normal no actúa transitivamente en la esfera es una órbita de la representación isotrópica de un espacio simétrico simple. b) ¿Existe alguna relación entre la noción de rango para espacios de curvatura no positiva y la noción de rango de una subvariedad? Respecto al rango de las variedades riemannianas se intenta probar un teorema general de descomposición para variedades riemannianas tal que toda geodésica esté contenida en un flat compacto. (...) Intentará generalizar los siguientes teoremas, válidos para flujos, a extensiones entre flujos, usando el concepto de semigrupo envolvente de una extensión. 1. X métrico y los elementos de E(X) son continuos, entonces E(X) es métrico. 2. Si se agrega la hipótesis de minimal, entonces X es equicontinuo. 3. X minimal, los elementos de E(X) de continuos y T contable entonces es equicontinuo. 4. X minimal y E(X) conmutativo entonces X es equicontinuo. 5. X distal y los elementos de E(X) son continuos, entonces X es equicontinuo.
Resumo:
FUNDAMENTO: O acúmulo de gordura visceral é considerado o principal fator de risco para doenças cardiovasculares e metabólicas. OBJETIVO: Determinar a prevalência de obesidade visceral e avaliar sua associação com fatores de risco cardiovasculares em mulheres jovens do Estado de Pernambuco. MÉTODOS: Estudo transversal, realizado com dados da "III Pesquisa Estadual de Saúde e Nutrição", envolvendo mulheres entre 25 e 36 anos. Avaliaram-se as variáveis: Índice de Massa Corporal (IMC), Circunferência da Cintura (CC), Razão Cintura-Estatura (RCE), Volume de Gordura Visceral (VGV) estimado por equação preditiva, Pressão Arterial Sistólica e Diastólica (PAS, PAD), Colesterol Total (CT), Triglicerídeo (TG), Glicemia de Jejum (GJ). RESULTADOS: Foram avaliadas 517 mulheres, com mediana de idade de 29 anos (27-32) e prevalência de obesidade visceral de 30,6%. Valores de IMC, PAS, PAD e TG foram superiores no grupo com obesidade visceral: IMC = 28,0 kg/m² (25,0 - 21,4) vs 23,9 kg/m² (21,5 - 26,4); PAS = 120,0 mmHg (110,0 - 130,0) vs 112,0 mmHg (100,0 - 122,0); PAD = 74 mmHg (70 - 80) vs 70 mmHg (63 - 80); TG = 156,0 mg/dL (115,0 - 203,2) vs 131,0 mg/dL (104,0 - 161,0), respectivamente, p < 0,01. Idade, PAS, PAD, TG e CT apresentaram correlação positiva e significante com o VGV: r = 0,171; 0,224; 0,163; 0,278; 0,124; respectivamente, p < 0,005. CONCLUSÃO: Verificou-se uma elevada prevalência de obesidade visceral, estando estatisticamente correlacionada a fatores de risco cardiovasculares.
Resumo:
FUNDAMENTO: Diversos autores correlacionaram o aumento do risco cardiovascular com o estado nutricional, porém existem diferentes critérios para a classificação de sobrepeso e obesidade em crianças. Objetivos: Avaliar o desempenho de três critérios de classificação nutricional em crianças, como definidores da presença de obesidade e preditores de níveis pressóricos elevados em escolares. MÉTODOS: Oitocentas e dezessete crianças de 6 a 13 anos matriculadas em escolas públicas do município de Vila Velha (ES) foram submetidas a avaliação antropométrica e de pressão arterial. A classificação quanto ao estado nutricional foi estabelecida mediante dois critérios internacionais (CDC/NCHS 2000 e IOTF 2000) e um critério brasileiro (Conde e Monteiro 2006). RESULTADOS: A prevalência de excesso de peso foi maior quando utilizado o critério de Conde e Monteiro (27%), e menor pelo critério do IOTF (15%). Pressão arterial elevada foi observada em 7,3% das crianças. Identificou-se forte associação entre a presença de excesso de peso e a ocorrência de níveis pressóricos elevados, independentemente do critério utilizado (p < 0,001). O critério que demonstrou maior sensibilidade em prever PA elevada foi o de Conde e Monteiro (44%), enquanto o de maior especificidade (94%), além de maior acurácia geral (63%), foi o do CDC. CONCLUSÕES: A prevalência de excesso de peso em crianças brasileiras é maior quando utilizado o critério de classificação de Conde e Monteiro, e menor quando utilizado o critério do IOTF. O critério de classificação brasileiro demonstrou ser o mais sensível como preditor de risco de PA elevada nessa amostra.
Resumo:
Size and shape in eggs of Rhode Island Red and Light Sussex breeds and in the hibrid Rhode x Sussex were studied. These characters are influenced by quantitative genes. Major and minor diameter were used for estimating size of the eggs and the ratio minor/major diameter for shape indice. It was found, in the material analyzed, that: a) the eggs laid by the sa- me chick are pratically uniform; b) the correlation coeficient between major and minor diameter is weak; c) Rhode Island Red has short eggs than Light Sussex; d) short eggs is dominant on long eggs; e) egg shape is the same in Rhode Island Red and Light Sussex breeds and different in the hibrid, which has rounder eggs than the breeds.
Resumo:
This paper deals with problems on population genetics in Hymenoptera and particularly in social Apidae. 1) The studies on populations of Hymenoptera were made according to the two basic types of reproduction: endogamy and panmixia. The populations of social Apinae have a mixed method of reproduction with higher percentage of panmixia and a lower of endogamy. This is shown by the following a) males can enter any hive in swarming time; b) males of Meliponini are expelled from hives which does not need them, and thus, are forced to look for some other place; c) Meliponini males were seen powdering themselves with pollen, thus becoming more acceptable in any other hive. The panmixia is not complete owing to the fact that the density of the breeding population as very low, even in the more frequent species as low as about 2 females and 160 males per reproductive area. We adopted as selection values (or survival indices) the expressions according to Brieger (1948,1950) which may be summarised as follows; a population: p2AA + ²pq Aa + q2aa became after selection: x p2AA + 2pq Aa + z q²aa. For alge-braics facilities Brieger divided the three selective values by y giving thus: x/y p2 AA + y/y 2 pq Aa + z/y q²aa. He called x/y of RA and z/y of Ra, that are survival or selective index, calculated in relation to the heterozygote. In our case all index were calculated in relation to the heterozygote, including the ones for haploid males; thus we have: RA surveval index of genotype AA Ra surveval index of genotype aa R'A surveval index of genotype A R'a surveval index of genotype a 1 surveval index of genotype Aa The index R'A ande R'a were equalized to RA and Ra, respectively, for facilities in the conclusions. 2) Panmitic populations of Hymenoptera, barring mutations, migrations and selection, should follow the Hardy-Weinberg law, thus all gens will be present in the population in the inicial frequency (see Graphifc 1). 3) Heterotic genes: If mutation for heterotic gene ( 1 > RA > Ra) occurs, an equilibrium will be reached in a population when: P = R A + Ra - 2R²a _____________ (9) 2(R A + Ra - R²A - R²a q = R A + Ra - 2R²A _____________ (10) 2(R A + Ra - R²A - R²a A heterotic gene in an hymenopteran population may be maintained without the aid of new mutation only if the survival index of the most viable mutant (RA) does not exced the limiting value given by the formula: R A = 1 + √1+Ra _________ 4 If RA has a value higher thah the one permitted by the formula, then only the more viable gene will remain present in the population (see Graphic 10). The only direct proof for heterotic genes in Hymenoptera was given by Mackensen and Roberts, who obtained offspring from Apis mellefera L. queens fertilized by their own sons. Such inbreeding resulted in a rapid loss of vigor the colony; inbred lines intercrossed gave a high hybrid vigor. Other fats correlated with the "heterosis" problem are; a) In a colony M. quadrifasciata Lep., which suffered severely from heat, the percentage of deths omong males was greater .than among females; b) Casteel and Phillips had shown that in their samples (Apis melifera L). the males had 7 times more abnormalities tian the workers (see Quadros IV to VIII); c) just after emerging the males have great variation, but the older ones show a variation equal to that of workers; d) The tongue lenght of males of Apis mellifera L., of Bombus rubicundus Smith (Quadro X), of Melipona marginata Lep. (Quadro XI), and of Melipona quadrifasciata Lep. Quadro IX, show greater variationthan that of workers of the respective species. If such variation were only caused by subviables genes a rapid increasse of homozigoty for the most viable alleles should be expected; then, these .wild populations, supposed to be in equilibrium, could .not show such variability among males. Thus we conclude that heterotic genes have a grat importance in these cases. 4) By means of mathematical models, we came to the conclusion tht isolating genes (Ra ^ Ra > 1), even in the case of mutations with more adaptability, have only the opor-tunity of survival when the population number is very low (thus the frequency of the gene in the breeding population will be large just after its appearence). A pair of such alleles can only remain present in a population when in border regions of two races or subspecies. For more details see Graphics 5 to 8. 5) Sex-limited genes affecting only females, are of great importance toHymenoptera, being subject to the same limits and formulas as diploid panmitic populations (see formulas 12 and 13). The following examples of these genes were given: a) caste-determining genes in the genus Melipona; b) genes permiting an easy response of females to differences in feeding in almost all social Hymenoptera; c) two genes, found in wild populations, one in Trigona (Plebéia) mosquito F. SMITH (quadro XII) and other in Melipona marginata marginata LEP. (Quadro XIII, colonies 76 and 56) showing sex-limited effects. Sex-limited genes affecting only males do not contribute to the plasticity or genie reserve in hymenopteran populations (see formula 14). 6) The factor time (life span) in Hymenoptera has a particular importance for heterotic genes. Supposing one year to be the time unit and a pair of heterotic genes with respective survival indice equal to RA = 0, 90 and Ra = 0,70 to be present; then if the life time of a population is either one or two years, only the more viable gene will remain present (see formula 11). If the species has a life time of three years, then both alleles will be maintained. Thus we conclude that in specis with long lif-time, the heterotic genes have more importance, and should be found more easily. 7) The colonies of social Hymenoptera behave as units in competition, thus in the studies of populations one must determine the survival index, of these units which may be subdivided in indice for egg-laying, for adaptive value of the queen, for working capacity of workers, etc. 8) A study of endogamic hymenopteran populations, reproduced by sister x brother mating (fig. 2), lead us to the following conclusions: a) without selection, a population, heterozygous for one pair of alleles, will consist after some generations (theoretically after an infinite number of generation) of females AA fecundated with males A and females aa fecundated with males a (see Quadro I). b) Even in endogamic population there is the theoretical possibility of the presence of heterotic genes, at equilibrium without the aid of new mutations (see Graphics 11 and 12), but the following! conditions must be satisfied: I - surveval index of both homozygotes (RA e Ra) should be below 0,75 (see Graphic 13); II - The most viable allele must riot exced the less viable one by more than is permited by the following formula (Pimentel Gomes 1950) (see Gra-fic 14) : 4 R5A + 8 Ra R4A - 4 Ra R³A (Ra - 1) R²A - - R²a (4 R²a + 4 Ra - 1) R A + 2 R³a < o Considering these two conditions, the existance of heterotic genes in endogamic populations of Hymenoptera \>ecames very improbable though not - impossible. 9) Genie mutation offects more hymenopteran than diploid populations. Thus we have for lethal genes in diploid populations: u = q2, and in Hymenoptera: u = s, being u the mutation ratio and s the frequency of the mutant in the male population. 10) Three factors, important to competition among species of Meliponini were analysed: flying capacity of workers, food gathering capacity of workers, egg-laying of the queen. In this connection we refer to the variability of the tongue lenght observed in colonies from several localites, to the method of transporting the pollen in the stomach, from some pots (Melliponi-ni storage alveolus) to others (e. g. in cases of pillage), and to the observation that the species with the most populous hives are almost always the most frequent ones also. 11) Several defensive ways used for Meliponini to avoid predation are cited, but special references are made upon the camouflage of both hive (fig. 5) and hive entrance (fig. 4) and on the mimetism (see list in page ). Also under the same heading we described the method of Lestrimelitta for pillage. 12) As mechanisms important for promoting genetic plasticity of hymenopteran species we cited: a) cytological variations and b) genie reserve. As to the former, duplications and numerical variations of chromosomes were studied. Diprion simile ATC was cited as example for polyploidy. Apis mellife-ra L. (n = 16) also sugests polyploid origen since: a) The genus Melipona, which belongs to a" related tribe, presents in all species so far studied n = 9 chromosomes and b) there occurs formation of dyads in the firt spermatocyte division. It is su-gested that the origin of the sex-chromosome of Apis mellifera It. may be related to the possible origin of diplo-tetraploidy in this species. With regards to the genie reserve, several possible types of mutants were discussed. They were classified according to their survival indices; the heterotic and neutral mutants must be considered as more important for the genie reserve. 13) The mean radius from a mother to a daghter colony was estimated as 100 meters. Since the Meliponini hives swarm only once a year we may take 100 meters a year as the average dispersion of female Meliponini in ocordance to data obtained from Trigona (tetragonisca) jaty F. SMITH and Melipona marginata LEP., while other species may give different values. For males the flying distance was roughly estimated to be 10 times that for females. A review of the bibliography on Meliponini swarm was made (pg. 43 to 47) and new facts added. The population desity (breeding population) corresponds in may species of Meliponini to one male and one female per 10.000 square meters. Apparently the males are more frequent than the females, because there are sometimes many thousands, of males in a swarm; but for the genie frequency the individuals which have descendants are the ones computed. In the case of Apini and Meliponini, only one queen per hive and the males represented by. the spermatozoos in its spermateca are computed. In Meliponini only one male mate with the queen, while queens of Apis mellijera L. are fecundated by an average of about 1, 5 males. (Roberts, 1944). From the date cited, one clearly sees that, on the whole, populations of wild social bees (Meliponini) are so small that the Sewall Wright effect may become of great importance. In fact applying the Wright's formula: f = ( 1/aN♂ + 1/aN♀) (1 - 1/aN♂ + 1/aN♀) which measures the fixation and loss of genes per generation, we see that the fixation or loss of genes is of about 7% in the more frequent species, and rarer species about 11%. The variation in size, tergite color, background color, etc, of Melipona marginata Lep. is atributed to this genetic drift. A detail, important to the survival of Meliponini species, is the Constance of their breeding population. This Constance is due to the social organization, i. e., to the care given to the reproductive individuals (the queen with its sperm pack), to the way of swarming, to the food storage intended to control variations of feeding supply, etc. 14) Some species of the Meliponini are adapted to various ecological conditions and inhabit large geographical areas (e. g. T. (Tetragonisca jaty F. SMITH), and Trigona (Nanno-trigona testaceicornis LEP.) while others are limited to narrow regions with special ecological conditions (e. g. M. fuscata me-lanoventer SCHWARZ). Other species still, within the same geographical region, profit different ecological conditions, as do M. marginata LEP. and M. quadrifasciata LEP. The geographical distribution of Melipona quadrifasciata LEP. is different according to the subspecies: a) subsp anthidio-des LEP. (represented in Fig. 7 by black squares) inhabits a region fron the North of the S. Paulo State to Northeastern Brazil, ,b) subspecies quadrifasciata LEP., (marked in Fig. 7 with black triangles) accurs from the South of S. Paulo State to the middle of the State of Rio Grande do Sul (South Brazil). In the margined region between these two areas of distribution, hi-brid colonies were found (Fig. 7, white circles); they are shown with more details in fig. 8, while the zone of hybridization is roughly indicated in fig. 9 (gray zone). The subspecies quadrifasciata LEP., has 4 complete yellow bands on the abdominal tergites while anthidioides LEP. has interrupted ones. This character is determined by one or two genes and gives different adaptative properties to the subspecies. Figs. 10 shows certains meteorological isoclines which have aproximately the same configuration as the limits of the hybrid zone, suggesting different climatic adaptabilities for both genotypes. The exis-tance of a border zone between the areas of both subspecies, where were found a high frequency of hybrids, is explained as follows: being each subspecies adapted to a special climatic zone, we may suppose a poor adaptation of either one in the border region, which is also a region of intermediate climatic conditions. Thus, the hybrids, having a combination of the parent qualities, will be best adapted to the transition zone. Thus, the hybrids will become heterotic and an equilibrium will be reached with all genotypes present in the population in the border region.
Resumo:
En aquest treball es presenta un nou mètode per a la inversió cega de funcions no-lineals mitjançant la gaussianització del senyal observat. El mètode es basa en restituir el caràcter aproximadament gaussià que presenta un senyal filtrat, gràcies al teorema del límit central,que ha vist canviada la seva distribució per l’efecte d’una funció no-lineal. Inicialment, doncs,aquest mètode és útil per a la inversió de sistemes de Wiener, tot i que en els darrers experiments realitzats s’han obtingut resultats interessants en sistemes purament no-lineals. El treball presenta dues possibles parametritzacions, la primera basada en xarxes neurals i la segona en polinomis. En els dos casos s’aconsegueix invertir la funció desconeguda sense tenir cap coneixement a priori ni del senyal original, ni del filtre, ni de la funció no-lineal que volem invertir.
Resumo:
We consider a delay differential equation with two delays. The Hopf bifurcation of this equation is investigated together with the stability of the bifurcated periodic solution, its period and the bifurcation direction. Finally, three applications are given.
Resumo:
"Vegeu el resum a l'inici del document del fitxer adjunt."
Resumo:
Uma amostra de T. cruzi foi isolada pela primeira vez de um exemplar do Triatoma costalimai, capturado no município de Mambai, Goiás. Estudos experimentais sobre infectividade e virulência foram conduzidos em triatomíneos, Calomys callosus (Rodentia) e camundongos albinos. Cultivo "In Vitro" da amostra isolada foi obtido com sucesso utilizando-se o meio LIT. As mensurações realizadas em tripomastigotas sanguícolas deram os seguintes resultados (mcg): comprimento total - 16,4 (± 1,1); flagelo livre - 4,9 (± 1,1); largura - 2,8 (± 0,6); distância NA - 4,8 (± 0,6); distância NP - 6,0 (± 0,5) e Indice nuclear 1,3.
Resumo:
Oitenta e uma macaubeiras (A. sclerocarpa) foram derrubadas e dissecadas na periferia de Belo Horizonte, no período de abril/ 1979 a julho/1980. Foram capturados 463 exemplares de Rhodnius neglectus, com uma taxa de infestação das palmeiras de 60,5% e uma média de 9,45% triatomineos/palmeira positiva. O R. neglectus nesta região parece apresentar uma unica geração anual, com possibilidade de duas, sendo que o periodo de oviposição se relaciona com os meses quentes do ano, coincidindo com a predominância de formas jovens sobre os adultos. A observação sugere que a densidade populacional do R. neglectus no seu ecotopo natural possa estar relacionada com a disponibilidade de alimento e com a presença de predadores como o Telenomus sp., formigas, aranhas, hemipteros, escorpiões e pseudo-escorpiões. O indice global de infecção pelo Trypanosoma cruzi foi de 15,9%, indicando o R. neglectus como um importante vetor silvestre deste tripanosomatídeo cuja principal fonte e constituída por marsupiais. O R. neglectus na regiao encontra-se estreitamente associado a palmeira de macaúba, e as aves que as frequentam constituem sua principal fonte alimentar. As observações não sugerem o R.neglectus como uma espécie transmissora do T. cruzi ao homem nesta região.
Resumo:
"vegeu el resum a l'inici del document del fitxer adjunt."
Resumo:
This work is focused on the development of a methodology for the use of chemical characteristic of tire traces to help answer the following question: "Is the offending tire at the origin of the trace found on the crime scene?". This methodology goes from the trace sampling on the road to statistical analysis of its chemical characteristics. Knowledge about the composition and manufacture of tread tires as well as a review of instrumental techniques used for the analysis of polymeric materials were studied to select, as an ansi vi cal technique for this research, pyrolysis coupled to a gas Chromatograph with a mass spectrometry detector (Py-GC/MS). An analytical method was developed and optimized to obtain the lowest variability between replicates of the same sample. Within-variability of the tread was evaluated regarding width and circumference with several samples taken from twelve tires of different brands and/or models. The variability within each of the treads (within-variability) and between the treads (between-variability) could be quantified. Different statistical methods have shown that within-variability is lower than between-variability, which helped differentiate these tires. Ten tire traces were produced with tires of different brands and/or models by braking tests. These traces have been adequately sampled using sheets of gelatine. Particles of each trace were analysed using the same methodology as for the tires at their origin. The general chemical profile of a trace or of a tire has been characterized by eighty-six compounds. Based on a statistical comparison of the chemical profiles obtained, it has been shown that a tire trace is not differentiable from the tire at its origin but is generally differentiable from tires that are not at its origin. Thereafter, a sample containing sixty tires was analysed to assess the discrimination potential of the developed methodology. The statistical results showed that most of the tires of different brands and models are differentiable. However, tires of the same brand and model with identical characteristics, such as country of manufacture, size and DOT number, are not differentiable. A model, based on a likelihood ratio approach, was chosen to evaluate the results of the comparisons between the chemical profiles of the traces and tires. The methodology developed was finally blindly tested using three simulated scenarios. Each scenario involved a trace of an unknown tire as well as two tires possibly at its origin. The correct results for the three scenarios were used to validate the developed methodology. The different steps of this work were useful to collect the required information to test and validate the underlying assumption that it is possible to help determine if an offending tire » or is not at the origin of a trace, by means of a statistical comparison of their chemical profile. This aid was formalized by a measure of the probative value of the evidence, which is represented by the chemical profile of the trace of the tire. - Ce travail s'est proposé de développer une méthodologie pour l'exploitation des caractéristiques chimiques des traces de pneumatiques dans le but d'aider à répondre à la question suivante : «Est-ce que le pneumatique incriminé est ou n'est pas à l'origine de la trace relevée sur les lieux ? ». Cette méthodologie s'est intéressée du prélèvement de la trace de pneumatique sur la chaussée à l'exploitation statistique de ses caractéristiques chimiques. L'acquisition de connaissances sur la composition et la fabrication de la bande de roulement des pneumatiques ainsi que la revue de techniques instrumentales utilisées pour l'analyse de matériaux polymériques ont permis de choisir, comme technique analytique pour la présente recherche, la pyrolyse couplée à un chromatographe en phase gazeuse avec un détecteur de spectrométrie de masse (Py-GC/MS). Une méthode analytique a été développée et optimisée afin d'obtenir la plus faible variabilité entre les réplicas d'un même échantillon. L'évaluation de l'intravariabilité de la bande de roulement a été entreprise dans sa largeur et sa circonférence à l'aide de plusieurs prélèvements effectués sur douze pneumatiques de marques et/ou modèles différents. La variabilité au sein de chacune des bandes de roulement (intravariabilité) ainsi qu'entre les bandes de roulement considérées (intervariabilité) a pu être quantifiée. Les différentes méthodes statistiques appliquées ont montré que l'intravariabilité est plus faible que l'intervariabilité, ce qui a permis de différencier ces pneumatiques. Dix traces de pneumatiques ont été produites à l'aide de pneumatiques de marques et/ou modèles différents en effectuant des tests de freinage. Ces traces ont pu être adéquatement prélevées à l'aide de feuilles de gélatine. Des particules de chaque trace ont été analysées selon la même méthodologie que pour les pneumatiques à leur origine. Le profil chimique général d'une trace de pneumatique ou d'un pneumatique a été caractérisé à l'aide de huitante-six composés. Sur la base de la comparaison statistique des profils chimiques obtenus, il a pu être montré qu'une trace de pneumatique n'est pas différenciable du pneumatique à son origine mais est, généralement, différenciable des pneumatiques qui ne sont pas à son origine. Par la suite, un échantillonnage comprenant soixante pneumatiques a été analysé afin d'évaluer le potentiel de discrimination de la méthodologie développée. Les méthodes statistiques appliquées ont mis en évidence que des pneumatiques de marques et modèles différents sont, majoritairement, différenciables entre eux. La méthodologie développée présente ainsi un bon potentiel de discrimination. Toutefois, des pneumatiques de la même marque et du même modèle qui présentent des caractéristiques PTD (i.e. pays de fabrication, taille et numéro DOT) identiques ne sont pas différenciables. Un modèle d'évaluation, basé sur une approche dite du likelihood ratio, a été adopté pour apporter une signification au résultat des comparaisons entre les profils chimiques des traces et des pneumatiques. La méthodologie mise en place a finalement été testée à l'aveugle à l'aide de la simulation de trois scénarios. Chaque scénario impliquait une trace de pneumatique inconnue et deux pneumatiques suspectés d'être à l'origine de cette trace. Les résultats corrects obtenus pour les trois scénarios ont permis de valider la méthodologie développée. Les différentes étapes de ce travail ont permis d'acquérir les informations nécessaires au test et à la validation de l'hypothèse fondamentale selon laquelle il est possible d'aider à déterminer si un pneumatique incriminé est ou n'est pas à l'origine d'une trace, par le biais d'une comparaison statistique de leur profil chimique. Cette aide a été formalisée par une mesure de la force probante de l'indice, qui est représenté par le profil chimique de la trace de pneumatique.