Introdução: No contexto do envelhecimento populacional, uma questão fundamental é avaliar se as estratégias de prevenção de doenças crônicas poderiam contribuir para o aumento dos anos vividos em boas condições de saúde, pela população idosa. Objetivo: Avaliar se a eliminação de determinadas doenças crônicas é capaz de levar à compressão da morbidade em indivíduos idosos. Métodos: Estudo transversal analítico, de base populacional, utilizando dados oficiais secundários para o Município de São Paulo, em 2000, e dados obtidos a partir do estudo SABE. O método de Sullivan foi utilizado para o cálculo de expectativas de vida livre de incapacidade (E.V.L.I.). O impacto da eliminação de uma doença na prevalência de incapacidade foi estimado com um modelo de regressão logística múltipla. Tábuas de vida de eliminação de causas foram utilizadas para calcular as probabilidades de morte com a eliminação de doenças. O efeito da eliminação das doenças crônicas foi avaliado, considerando a teoria de riscos competitivos e a abordagem proposta por Nusselder e colaboradores. Resultados: Os maiores ganhos em E.V.L.I., com a eliminação de doenças crônicas, ocorreram no sexo feminino, levando a um processo de compressão absoluta da morbidade. Nos indivíduos de idade mais avançada, os ganhos em E.V.L.I., ocorreram em função de um processo de compressão relativa da morbidade. Nos homens com idade de 75 anos, todas as doenças estudadas, com exceção da doença cardíaca e da hipertensão arterial sistêmica, levaram a um processo de expansão absoluta da morbidade, mas simultaneamente a um processo de compressão relativa da morbidade, ao serem eliminadas. A doença cardíaca apresentou-se como aquela que mais promoveria a compressão da morbidade, caso fosse eliminada, em ambos os sexos. Conclusão: A eliminação de doenças crônicas na população idosa poderia levar a uma compressão da morbidade em homens e mulheres, tanto na idade de 60 anos, quanto na de 75 anos / Introduction: In the context of the aging process, a key issue is to assess whether strategies to prevent chronic diseases may contribute to the increase in years lived in good health among elderly individuals. Objective: To evaluate whether elimination of certain chronic diseases can lead to the compression of morbidity, in the elderly. Methods: Analytical cross-sectional survey, based on official data for the city of São Paulo, in 2000, and data obtained from the SABE study. Sullivans method was used for the calculation of disability-free life expectancy (DFLE). Cause-deleted disability prevalence was estimated using multiple logistic regression model. Cause-deleted probabilities of dying were derived with the cause-elimination life-table technique, considering the independence of the causes of based on the approach proposed by Nusselder and co-workers. Results: The greatest gains in DFLE, with the elimination of chronic diseases, occurred in women, leading to a process of absolute compression of morbidity. Among individuals of a more advanced age, gains in DFLE occurred due to a relative compression of morbidity process. Among men aged 75 years, all diseases eliminated, except heart disease and hypertension, led to a process of absolute expansion of morbidity, but simultaneously, to a relative compression of morbidity. If eliminated, heart disease was the condition that would most lead to the compression of morbidity in both genders. Conclusion: The elimination of chronic diseases in the elderly population could lead to the compression of morbidity in men and women at both 60 years of age and in 75 years of age or older

Application of (geo)demographic methods in education Abstract This master's thesis presents the possibilities of application of demographic, geodemographic and statistical methods on data published by the educational sector. The methods of demographic analysis are represented by the usage of rates, the concept of multistate demography (Markov chains) and the application of life tables. The enrollment ratio at particular levels of education, the average length of schooling and the number of dropouts from school grades are evaluated by these procedures. Markov chains which are based on the probabilities of transition between grades are also examined in terms of their use for forecasting purposes. These methods analyze the situation at the preschool, primary and secondary levels and are used on data from the annual Statistical Yearbooks on Education. In the field of geodemography, the so called preferential model of migration flows is presented. This model examines how applicants for tertiary education prefer or reject the regions of the Czech Republic for their tertiary education studies. The last method is the binary logistic regression which analyzes the inequalities in access to tertiary education. Both preferential model and logistic regression are based on data files on the admission process at...

There is anecdotal evidence that populations of the New Zealand endemic red admiral butterfly Bassaris gonerilla (F.) have declined since the early 1900s. This decline has been associated with the introduction of the generalist pupal parasitoids Pteromalus puparum (L.) and Echthromorpha intricatoria (F.). The former was deliberately introduced for the biological control of the cabbage white butterfly (Pieris rapae (L.)); the latter is an adventitious arrival from Australia. The objective of this thesis was to quantify, using population models, the effect that P. puparum is having on B. gonerilla abundance. Population monitoring and a phenology model (based on temperature-related development rates) indicated that B. gonerilla has two full generations and one partial generation per summer in the Banks Peninsula region of New Zealand. B. gonerilla abundance was greatly reduced in drought summers, which was probably due to the negative effects of drought on the quality and quantity of the larval host plant Urtica ferox Forst. A life table study showed that egg parasitism by the unidentified scelionid Telenomus sp. was the largest mortality factor for the pre-imaginal stages of B. gonerilla, followed by "disappearance" mortality (predation and dispersal) in the larval stages. Pupal mortality due to P. puparum was lower compared with that caused by E. intricatoria, with 1-19% and 20-30% of pupae being parasitised by P. puparum and E. intricatoria, respectively. Collection of B. gonerilla pupae from the Christchurch, Dunedin and Wellington areas confirmed higher rates of percentage parasitism by E. intricatoria. B. gonerilla collected from the Banks Peninsula had a 50: 50 sex ratio and lifetime fecundity was estimated in the laboratory as 312 eggs per female. There was no evidence of density-dependent parasitism of B. gonerilla pupae by P. puparum in the field, although there was a significant positive relationship between life table estimates of E. intricatoria parasitism and B. gonerilla pupal abundance. Larval dispersal from the host plant showed a positive relationship with larval instar but no relationship with larval density. Rates of change in B. gonerilla adult abundance between generations within a year showed evidence of density dependence, and this negative feedback was stronger in a drought year. A discrete-time model for B. gonerilla population dynamics was constructed which had two summer generations per year and a partial overwintering generation. The model showed that the presence of this overwintering generation provides a temporal refuge from high levels of E. intricatoria parasitism. Removal of parasitoid mortality from the model suggested that P. puparum was suppressing B. Gonerilla populations on the Banks Peninsula by 5% and E. intricatoria by 30%. An important assumption of the model was that parasitism rates were independent of B. gonerilla density. This assumption appears valid for P. puparum parasitism, but may not be valid for E. intricatoria; therefore the estimated suppression levels due to this adventive parasitoid should be viewed with some caution. It is too soon to generalise on what determines the magnitude of non-target effects by arthropod biocontrol agents, this being only the second study to quantify effects at a population level. However, in this case retrospective analysis has shown that the impact of non-target parasitism by P. puparum on B. gonerilla abundance has been small. There is anecdotal evidence that populations of the New Zealand endemic red admiral butterfly Bassaris gonerilla (F.) have declined since the early 1900s. This decline has been associated with the introduction of the generalist pupal parasitoids Pteromalus puparum (L.) and Echthromorpha intricatoria (F.). The former was deliberately introduced for the biological control of the cabbage white butterfly (Pieris rapae (L.)); the latter is an adventitious arrival from Australia. The objective of this thesis was to quantify, using population models, the effect that P. puparum is having on B. gonerilla abundance. Population monitoring and a phenology model (based on temperature-related development rates) indicated that B. gonerilla has two full generations and one partial generation per summer in the Banks Peninsula region of New Zealand. B. gonerilla abundance was greatly reduced in drought summers, which was probably due to the negative effects of drought on the quality and quantity of the larval host plant Urtica ferox Forst.. A life table study showed that egg parasitism by the unidentified scelionid Telenomus sp. was the largest mortality factor for the pre-imaginal stages of B. gonerilla, followed by "disappearance" mortality (predation and dispersal) in the larval stages. Pupal mortality due to P. puparum was lower compared with that caused by E. intricatoria, with 1-19% and 20-30% of pupae being parasitised by P. puparum and E. intricatoria, respectively. Collection of B. gonerilla pupae from the Christchurch, Dunedin and Wellington areas confirmed higher rates of percentage parasitism by E. intricatoria. B. gonerilla collected from the Banks Peninsula had a 50: 50 sex ratio and lifetime fecundity was estimated in the laboratory as 312 eggs per female. There was no evidence of density-dependent parasitism of B. gonerilla pupae by P. puparum in the field, although there was a significant positive relationship between life table estimates of E. intricatoria parasitism and B. gonerilla pupal abundance. Larval dispersal from the host plant showed a positive relationship with larval instar but no relationship with larval density. Rates of change in B. gonerilla adult abundance between generations within a year showed evidence of density dependence, and this negative feedback was stronger in a drought year. A discrete-time model for B. gonerilla population dynamics was constructed which had two summer generations per year and a partial overwintering generation. The model showed that the presence of this overwintering generation provides a temporal refuge from high levels of E. intricatoria parasitism. Removal of parasitoid mortality from the model suggested that P. puparum was suppressing B. Gonerilla populations on the Banks Peninsula by 5% and E. intricatoria by 30%. An important assumption of the model was that parasitism rates were independent of B. gonerilla density. This assumption appears valid for P. puparum parasitism, but may not be valid for E. intricatoria; therefore the estimated suppression levels due to this adventive parasitoid should be viewed with some caution. It is too soon to generalise on what determines the magnitude of non-target effects by arthropod biocontrol agents, this being only the second study to quantify effects at a population level. However, in this case retrospective analysis has shown that the impact of non-target parasitism by P. puparum on B. gonerilla abundance has been small.