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Doctor of Philosophy (PhD) / The Australian cotton industry has developed high yielding and high quality fibre production systems and attributes a significant contribution of this achievement to highly innovative breeding programs, specifically focused on the production of premium quality lint for the export market. Breeding programs have recently shifted attention to the development of new germplasm with superior stress tolerance to minimise yield losses attributed to adverse environmental conditions and inputs such as irrigation, fertilisers and pesticides. Various contributors to yield, such as physiology, biochemistry and gene expression have been implemented as screening tools for tolerance to high temperatures under growth cabinet and laboratory conditions but there has been little extension of these mechanisms to field based systems. This study evaluates tools for the identification of specific genotypic thermotolerance under field conditions using a multi-level ‘top down’ approach from crop to gene level. Field experiments were conducted in seasons 1 (2006) and 3 (2007) at Narrabri (Australia) and season 2 (2006) in Texas (The United States of America) and were supplemented by growth cabinet experiments to quantify cultivar differences in yield, physiology, biochemical function and gene expression under high temperatures. Whole plants were subjected to high temperatures in the field through the construction of Solarweave® tents and in the growth cabinet at a temperature of 42 oC. The effectiveness of these methods was then evaluated to establish a rapid and reliable screening tool for genotype specific thermotolerance that could potentially improve the efficiency of breeding programs and aid the development to high yielding cultivars for hot growing regions. Cotton cultivars Sicot 53 and Sicala 45 were evaluated for thermotolerance using crop level measurements (yield and fibre quality) and whole plant measurements (fruit retention) to determine the efficacy of these measurements as screening tools for thermotolerance under field conditions. Sicot 53 was selected as a relatively thermotolerant cultivar whereas Sicala 45 was selected as a cultivar with a lower relative thermotolerance and this assumption was made on the basis of yield in hot and cool environments under the CSIRO Australian cotton breeding program. Yield and fruit retention were lower under tents compared with ambient conditions in all 3 seasons. Yield and fruit retention were highly correlated in season 1 and were higher for Sicot 53 compared to Sicala 45 suggesting that fruit retention is a primary limitation to yield in a hot season. Thus yield and fruit retention are good indicators of thermotolerance in a hot season. Temperature treatment and cultivar differences were determined for fibre quality in seasons 1 and 3; however, quality exceeded the industry minimum thereby indicating that fibre quality is not a good determinant of thermotolerance. Physiological determinants of plant functionality such as photosynthesis, electron transport rate, stomatal conductance and transpiration rate were determined for cultivars Sicot 53 and Sicala 45 under the tents and an index of these parameters was also analysed to determine overall plant physiological capacity in the field. Physiological capacity was also determined under high temperatures in the growth cabinet using a light response curve at various levels of photosynthetically active radiation (PAR). Photosynthesis and electron transport rate decreased, whilst stomatal conductance and transpiration rate increased under the tents as well as under high temperatures in the growth cabinet. Photosynthesis and electron transport rate were higher for Sicot 53 but stomatal conductance and transpiration rate were higher for Sicala 45 under the tents. No cultivar differentiation was evident for plants grown under high temperatures in the growth cabinet. Temperature treatment and cultivar differences in physiological function were greater in a hot year (season 1), thereby indicating the importance of cultivar selection for thermotolerance in the presence of stress. Electron transport rate was correlated with yield in season 1, thus suggesting the suitability of this method for broad genotypic screening for thermotolerance under field conditions. Biochemical processes such as membrane integrity and enzyme viability were used to determine cultivar specific thermotolerance under high temperature stress in the laboratory, field and growth cabinet. Electrolyte leakage is an indicator of decreased membrane integrity and may be estimated by the relative electrical conductivity or relative cellular injury assays. The heat sensitivity of dehydrogenase activity, a proxy for cytochrome functionality and capacity for mitochondrial electron transport, may be quantified spectrophotometrically. Cellular membrane integrity and enzyme viability decreased sigmoidally with exposure to increasing temperatures in a water bath. Membrane integrity was higher for Sicot 53 compared with Sicala 45 under the tents and under high temperatures in the growth cabinet. No temperature treatment or cultivar differences were found for enzyme viability under the tents; however, enzyme viability for Sicala 45 was higher in the growth cabinet compared with Sicot 53. Relative electrical conductivity was strongly correlated with yield under ambient field conditions and under the tents, suggesting impairment of electron flow through photosynthetic and/or respiratory pathways, thus contributing to lower potential for ATP production and energy generation for yield contribution. Thus, the membrane integrity assay was considered to be a rapid and reliable tool for thermotolerance screening in cotton cultivars. Gene expression was examined for cultivars Sicot 53 and Sicala 45 grown under high (42 oC) temperatures in the growth cabinet. Rubisco activase expression was quantified using quantitative real-time polymerase chain reaction analysis and was decreased under high temperatures and was lower for Sicala 45 than Sicot 53. Maximum cultivar differentiation was found after 1.0 h exposure to high temperatures and hence, leaf tissue sampled from this time point was further analysed for global gene profiling using cDNA microarrays. Genes involved in metabolism, heat shock protein generation, electron flow and ATP generation were down-regulated under high temperatures in the growth cabinet and a greater number of genes were differentially expressed for Sicala 45, thereby indicating a higher level of heat stress and a greater requirement for mobilisation of protective and compensatory mechanisms compared with Sicot 53. Cultivar specific thermotolerance determination using gene profiling may be a useful tool for understanding the underlying basis of physiological and biochemical responses to high temperature stress in the growth cabinet. There is future opportunity for profiling genes associated with heat stress and heat tolerance for identification of key genes associated with superior cultivar performance under high temperature stress and characterisation of these genes under field conditions. This research has identified cultivar differences in yield under field conditions and has identified multiple physiological and biochemical pathways that may contribute to these differences. Future characterisation of genes associated with heat stress and heat tolerance under growth cabinet conditions may be extended to field conditions, thus providing the underlying basis of the response of cotton to high temperature stress. Electron transport rate and relative electrical conductivity were found to be rapid and reliable determinants of cultivar specific thermotolerance and hence may be extended to broad-spectrum screening of a range of cotton cultivars and species and under a range of abiotic stress. This will enable the identification of superior cotton cultivars for incorporation into local breeding programs for Australian and American cotton production systems.

Doctor of Philosophy (PhD) / The Australian cotton industry has developed high yielding and high quality fibre production systems and attributes a significant contribution of this achievement to highly innovative breeding programs, specifically focused on the production of premium quality lint for the export market. Breeding programs have recently shifted attention to the development of new germplasm with superior stress tolerance to minimise yield losses attributed to adverse environmental conditions and inputs such as irrigation, fertilisers and pesticides. Various contributors to yield, such as physiology, biochemistry and gene expression have been implemented as screening tools for tolerance to high temperatures under growth cabinet and laboratory conditions but there has been little extension of these mechanisms to field based systems. This study evaluates tools for the identification of specific genotypic thermotolerance under field conditions using a multi-level ‘top down’ approach from crop to gene level. Field experiments were conducted in seasons 1 (2006) and 3 (2007) at Narrabri (Australia) and season 2 (2006) in Texas (The United States of America) and were supplemented by growth cabinet experiments to quantify cultivar differences in yield, physiology, biochemical function and gene expression under high temperatures. Whole plants were subjected to high temperatures in the field through the construction of Solarweave® tents and in the growth cabinet at a temperature of 42 oC. The effectiveness of these methods was then evaluated to establish a rapid and reliable screening tool for genotype specific thermotolerance that could potentially improve the efficiency of breeding programs and aid the development to high yielding cultivars for hot growing regions. Cotton cultivars Sicot 53 and Sicala 45 were evaluated for thermotolerance using crop level measurements (yield and fibre quality) and whole plant measurements (fruit retention) to determine the efficacy of these measurements as screening tools for thermotolerance under field conditions. Sicot 53 was selected as a relatively thermotolerant cultivar whereas Sicala 45 was selected as a cultivar with a lower relative thermotolerance and this assumption was made on the basis of yield in hot and cool environments under the CSIRO Australian cotton breeding program. Yield and fruit retention were lower under tents compared with ambient conditions in all 3 seasons. Yield and fruit retention were highly correlated in season 1 and were higher for Sicot 53 compared to Sicala 45 suggesting that fruit retention is a primary limitation to yield in a hot season. Thus yield and fruit retention are good indicators of thermotolerance in a hot season. Temperature treatment and cultivar differences were determined for fibre quality in seasons 1 and 3; however, quality exceeded the industry minimum thereby indicating that fibre quality is not a good determinant of thermotolerance. Physiological determinants of plant functionality such as photosynthesis, electron transport rate, stomatal conductance and transpiration rate were determined for cultivars Sicot 53 and Sicala 45 under the tents and an index of these parameters was also analysed to determine overall plant physiological capacity in the field. Physiological capacity was also determined under high temperatures in the growth cabinet using a light response curve at various levels of photosynthetically active radiation (PAR). Photosynthesis and electron transport rate decreased, whilst stomatal conductance and transpiration rate increased under the tents as well as under high temperatures in the growth cabinet. Photosynthesis and electron transport rate were higher for Sicot 53 but stomatal conductance and transpiration rate were higher for Sicala 45 under the tents. No cultivar differentiation was evident for plants grown under high temperatures in the growth cabinet. Temperature treatment and cultivar differences in physiological function were greater in a hot year (season 1), thereby indicating the importance of cultivar selection for thermotolerance in the presence of stress. Electron transport rate was correlated with yield in season 1, thus suggesting the suitability of this method for broad genotypic screening for thermotolerance under field conditions. Biochemical processes such as membrane integrity and enzyme viability were used to determine cultivar specific thermotolerance under high temperature stress in the laboratory, field and growth cabinet. Electrolyte leakage is an indicator of decreased membrane integrity and may be estimated by the relative electrical conductivity or relative cellular injury assays. The heat sensitivity of dehydrogenase activity, a proxy for cytochrome functionality and capacity for mitochondrial electron transport, may be quantified spectrophotometrically. Cellular membrane integrity and enzyme viability decreased sigmoidally with exposure to increasing temperatures in a water bath. Membrane integrity was higher for Sicot 53 compared with Sicala 45 under the tents and under high temperatures in the growth cabinet. No temperature treatment or cultivar differences were found for enzyme viability under the tents; however, enzyme viability for Sicala 45 was higher in the growth cabinet compared with Sicot 53. Relative electrical conductivity was strongly correlated with yield under ambient field conditions and under the tents, suggesting impairment of electron flow through photosynthetic and/or respiratory pathways, thus contributing to lower potential for ATP production and energy generation for yield contribution. Thus, the membrane integrity assay was considered to be a rapid and reliable tool for thermotolerance screening in cotton cultivars. Gene expression was examined for cultivars Sicot 53 and Sicala 45 grown under high (42 oC) temperatures in the growth cabinet. Rubisco activase expression was quantified using quantitative real-time polymerase chain reaction analysis and was decreased under high temperatures and was lower for Sicala 45 than Sicot 53. Maximum cultivar differentiation was found after 1.0 h exposure to high temperatures and hence, leaf tissue sampled from this time point was further analysed for global gene profiling using cDNA microarrays. Genes involved in metabolism, heat shock protein generation, electron flow and ATP generation were down-regulated under high temperatures in the growth cabinet and a greater number of genes were differentially expressed for Sicala 45, thereby indicating a higher level of heat stress and a greater requirement for mobilisation of protective and compensatory mechanisms compared with Sicot 53. Cultivar specific thermotolerance determination using gene profiling may be a useful tool for understanding the underlying basis of physiological and biochemical responses to high temperature stress in the growth cabinet. There is future opportunity for profiling genes associated with heat stress and heat tolerance for identification of key genes associated with superior cultivar performance under high temperature stress and characterisation of these genes under field conditions. This research has identified cultivar differences in yield under field conditions and has identified multiple physiological and biochemical pathways that may contribute to these differences. Future characterisation of genes associated with heat stress and heat tolerance under growth cabinet conditions may be extended to field conditions, thus providing the underlying basis of the response of cotton to high temperature stress. Electron transport rate and relative electrical conductivity were found to be rapid and reliable determinants of cultivar specific thermotolerance and hence may be extended to broad-spectrum screening of a range of cotton cultivars and species and under a range of abiotic stress. This will enable the identification of superior cotton cultivars for incorporation into local breeding programs for Australian and American cotton production systems.

O nematóide das lesões Pratylenchus coffeae é um dos principais parasitos do cafeeiro e de outras culturas e sua variabilidade biológica, que dificulta a adoção de métodos de controle, contribui para aumentar a sua importância no Brasil. Pela importância da cafeicultura e a falta de estudos com esse nematóide no Brasil, foram realizados experimentos com dois de seus isolados (K5 e M2), com os objetivos de correlacionar densidades populacionais do nematóide aos danos causados e estabelecer possíveis fontes de resistência de cafeeiros ao isolado K5. Foram testadas diferentes densidades populacionais iniciais do isolado M2 em plantas (seis pares de folhas) e plântulas (dois pares de folhas) do cafeeiro arábico ‘Catuaí Vermelho’. As densidades populacionais utilizadas foram de 0, 333, 1.000, 3.000 e 9.000 nematóides por plântula ou planta. A avaliação ocorreu aproximadamente cinco (plântulas) e sete (plantas) meses após a inoculação. Os resultados mostraram que houve uma acentuada redução do crescimento das plântulas, bem como massa fresca das raízes e massa seca da parte aérea, já a partir das densidades mais baixas. A variação populacional (Pf/Pi) foi menor que um (1,0) para todas as densidades de inóculo, indicando que esta cultivar, no estágio de plântulas com dois pares de folhas, mostrou-se intolerante ao parasitismo. Em relação à inoculação das plantas, já com seis pares de folhas, não houve diferenças significativas nas variáveis analisadas e ocorreram decréscimos populacionais do nematóide, indicando que, nessas condições, ‘Catuaí Vermelho’ mostrou-se resistente ao isolado M2. Em relação ao isolado K5, foram realizados cinco experimentos, visando caracterizar as reações de genótipos de Coffea canephora ('Robusta' e 'Conilon'), além de C. arabica ‘Mundo Novo’, comparado às reações frente ao nematóide de galhas Meloidogyne incognita raça 2. No Experimento 1, foram utilizadas plantas de C. arabica ‘Mundo Novo’, inoculadas com 1.480 nematóides por planta (isolado K5 e M. incognita). Após sete meses da inoculação foi feita a avaliação, mostrando que o crescimento populacional dos nematóides foi alto e a reação de suscetibilidade. Mesmo em mudas desenvolvidas de cafeeiro ‘Mundo Novo’, o isolado K5 destacou-se como tão agressivo quanto M. incognita. Os outros genótipos testados, de C. canephora, foram inoculados com 3.000 nematóides por planta. Nos Experimentos 2 e 3, as linhagens IAC 4804 e IAC 4810 de ‘Robusta’ foram suscetíveis ao isolado K5, mas em um deles (IAC 4804) ocorreu grande variação entre as repetições em relação à M. incognita. Apenas o isolado K5 promoveu redução do crescimento do cafeeiro, evidenciado na variável massa fresca das raízes, em ambas as linhagens, sendo que IAC 4810 comportou-se como resistente a M. incognita. No caso de C. canephora ‘Conilon’, ambas as linhagens testadas (IAC 4764 e IAC 4765) foram resistentes ao isolado K5 e suscetíveis a M. incognita. / The lesion-nematode Pratylenchus coffeae is a major pest of coffee and other economic crops and its biological variability, which often makes difficult the adoption of control methods, contributes to increase the importance of this parasite in Brazil. Due to the importance of coffee production and the lack of studies involving this nematode species in Brazil, experiments were set with two of its available isolates (K5 and M2) to correlate initial population densities with the damage caused on coffee plants and to establish possible resistance sources in relation to the isolate K5. Different population densities of isolate M2 were tested in plants (six pairs of leaves) and seedlings (two pairs of leaves) of Coffea arabica ‘Catuaí Vermelho’. The population densities (Pi) were: 0, 333, 1.000, 3.000 and 9.000 nematodes per seedling or plant. The evaluation was done at approximately five (seedlings) and seven (plants) months after inoculation. The results showed that there was a marked reduction of the height, as well as root fresh weight and shoot dry weight of the seedlings, starting from the lower Pi values. The nematode population decreased (Pf/Pi < 1), indicating that this cultivar, at the seedling stage, was intolerant to parasitism. In relation to the inoculation of older plants, there were no significant differences in the growth parameters and the nematode population also decreased allowing ‘Catuaí Vermelho’ to be rated as resistant to the isolate M2. In relation to isolate K5, five experiments (referred to as 1, 2, 3, 4, and 5) were set to characterize the reaction of different genotypes of Coffea canephora ('Robusta' and 'Conilon') and C. arabica ‘Mundo Novo', as compared with their reaction to the root-knot nematode Meloidogyne incognita race 2. In Experiment 1, plants of C. arabica ‘Mundo Novo’ were inoculated with 1,480 nematodes per plant (K5 and M. incognita). The final evaluation after seven months of the inoculation showed a high populational increase of the nematodes and that both were pathogenic at a same extent. The other genotypes tested, belonging to C. canephora, were inoculated with 3,000 nematodes per plant. The genotypes (IAC 4804 and IAC 4810) of ‘Robusta’ were susceptible to isolate K5, but in one of them (IAC 4804) there was great variation among the repetitions in relation to M. incognita. The isolate K5 caused marked reduction in the growth of coffee Robusta plants as evidenced particularly through the root fresh weight values in both tested genotypes; in addition, IAC 4810 was rated as resistant to M. incognita. With regard to C. canephora 'Conilon', both tested genotypes (IAC 4764 and IAC 4765) were resistant to isolate K5 and susceptible to M. incognita.

A cana-de-açúcar é uma das principais culturas agroindustriais do Brasil, sendo amplamente cultivada para a produção de açúcar e etanol. Esta cultura se torna a cada dia mais importante no cenário mundial, devido à busca constante por fontes de energia alternativas e mais sustentáveis. Para atender a crescente demanda, é necessária a liberação frequente de novas variedades, mais adaptadas às regiões de cultivo e tolerantes às alterações ambientais. Assim, o estabelecimento da metodologia de transformação genética além de contribuir para o estudo funcional de genes de interesse é uma metodologia alternativa para obtenção de novas variedades. O processo de obtenção de transgênicos é dependente de um eficiente protocolo de regeneração de plantas in vitro, que geralmente envolve uma fase de formação de células indiferenciadas (calos). A indução e a manutenção dos calos são favoráveis ao aumento da atividade de elementos de transposição (ETs) os quais são muito freqüentes no genoma de cana e podem acarretar variabilidade no genoma vegetal pela alteração dos padrões e funções gênicas devido a essa mobilização, afrontando a fidelidade genética dos cultivares transgênicos obtidos. Baseando-se na importância de reduzir o período de cultura de tecidos e controlar a atividade dos ETs durante o desenvolvimento in vitro, o objetivo desse trabalho foi buscar alternativas no controle e na redução do tempo para regeneração de plantas, inclusive com a aplicação de peptídeos hormonais, assim como de transformar geneticamente as variedades RB835089 e RB835486 com o gene Ddm1 de Arabidopsis, visando o silenciamento dos elementos de transposição em cana-de-açúcar. Para isso, foram analisados os meios de cultura MS3c e ML1G1 e o efeito da água de coco na indução e formação de calos como também na regeneração de plantas. Foram testados os meios de regeneração de plantas MSAc, SRM, ML1R3 e ML1R4, obtendo-se em média 5,2 plantas por explante no meio MSAc, que foi superior aos demais meios. Este meio foi utilizado para testar o efeito individual dos peptídeos hormonais CLV3 e PSK- em calos embriogênicos, os quais apresentaram acréscimo na regeneração de plantas para 9,3 plantas por explantes com doses de 30 µM de PSK-a. A transformação genética por biolística através da cotransformação dos genes neo e AtDdm1 resultou em 34 plantas transgênicas. O estudo da mobilização dos ETs durante o desenvolvimento in vitro foi realizado para quatro retrotransposons. A expressão heteróloga do gene AtDdm1 em cana-de-açúcar mostrou atuar no controle da expressão do retroelemento TE010. O estudo da mobilização dos retrotransposons e do gene Ddm1 endógeno de cana (SsDdm1) durante o desenvolvimento in vitro confirmou que o gene SsDdm1 foi chave no controle da expressão dos retroelementos. A transformação genética com o gene AtDdm1 aliada a rápida regeneração de plantas a partir de discos foliares possibilitam condições que minimizam a expressão dos ETs em cana-de-açúcar. / Sugarcane is one of the major agro-industrial crops of Brazil being widely cultivated for the production of sugar and ethanol. This culture has become increasingly more important on the world stage each day due to the constant search for alternative and sustainable energy sources. In order to meet growing demand, it is necessary to often release new varieties, better adapted to cultivated expansion area and tolerant to environmental changes. Thus, the establishing of genetic transformation methodology beyond of contributing to the functional study of genes of interest and it is an alternative method for obtaining new varieties. The process of obtaining transgenic plants is dependent of an efficient protocol for in vitro plant regeneration, which generally involves a phase of undifferentiated cells (callus). The induction and maintenance of callus are favorable to increase the activity of transposable elements (TEs) which are very frequent in the genome of sugarcane and may cause variability in the plant genome by altering patterns and gene functions due to this mobilization, confronting the genetic fidelity of the transgenic cultivars obtained. Based on the importance of reducing the period of tissue culture and control the activity of TEs during in vitro development, the objective of this work was to seek alternatives to control and reduce the time for plant regeneration, including the use of peptides hormone, as well as to genetically transform sugarcane varieties RB835089 and RB835486 with the Ddm1 Arabidopsis gene to silence the transposable elements in cane sugar. For this, we tested the culture media MS3c and ML1G1and the effect of coconut water in callus induction and growth as well as on plant regeneration. We tested the plant regeneration media MSAc, SRM, ML1R3 and ML1R4, obtaining an average of 5.2 plants per explants using MSAC, superior to other medium tested. It was used to test the individual effect of peptides hormones such as CLV3 and PSK- in embryogenic callus, which showed an increase in plant regeneration to 9.3 plants per explant with doses of 30µM PSK-a. Genetic co-transformation with the neo and AtDdm1 genes by biolistic resulted in 34 transgenic plants. A study of TEs during in vitro development was performed for four retrotransposons. Heterologous expression of the AtDdm1 gene in sugarcane showed to control the expression of the retroelement TE010. The study of mobilization of retrotransposons and the endogenous Ddm1 gene (SsDdm1) during in vitro development confirmed that SsDdm1 was key gene in controlling the expression of retrotransposons. Genetic transformation with the AtDdm1 gene and the fast regeneration of plants provide positive conditions to minimize the expression of ETs in sugarcane.

O vírus sincicial respiratório humano (VSRH) é o agente viral mais freqüentemente relacionado a doenças do trato respiratório inferior em crianças abaixo de um ano de idade. Analíse da varibilidade antigênica e gênica mostraram que o VSRH pode ser divido em dois grupos: A e B. O vírus é um membro do gênero Pneumovirus pertencente a família Paramyxoviridea, e possui três principais proteínas que são: glicoproteina F (fusão), glicoproteina G (adesão), glicoproteina SH (pequena proteína hidrofóbica). A proteína F é responsável pela fusão da célula ao vírus, enquanto a proteína G tem papel fundamental na replicação do vírus, porém a função da proteína SH, ainda não está bem definida, estudos recentes mostram-na como responsável por inibir a sinalização do fator de necrose tumoral alfa (TNF-a). Neste estudo foram colhidas amostras de 965 crianças, entre os anos de 2004 e 2005, dentre as quais 424 foram positivas. 117 amostras foram seqüenciadas a proteína SH e G e comparadas com amostras que circularam mundialmente. A analíse filogenética mostrou uma baixa variabilidade entre os genótipos estudados tanto do grupo A quanto do B. / The human respiratory syncytial virus (HRSV) is the major cause of lawer respiratory tract infections in infantis, young children and elderly. Analysis of the antigenic and genetic variability has shown that there are two groups of the virus HRSV, A and B. The virus (HRSV) is a member of the genus pneumovirus in the paramyxoviridae family. The virus encodes three membrane-bound glicoproteins, namely the fusion (F) attachment (G) and small hydrophobic (SH) proteins. The F mediates fusion of the virus and cell membranes and the G proteins is involved in virus attachment. The biological properties of the F and G glicoproteins and role that they play during virus replication relatively well understood, however the functional significance of the SH protein during replication remains unclear, although recent study shown that it can inhibit TNF-alpha. In this study, HRSV strains were isolated from nasopharyngeal aspirates collected from 965 children between 2004 and 2005, yielding 424 positive samples. We sequenced the small hydrophobic protein (SH) gene and protein (G) of 117 samples and compared them with other viruses identified worldwide. The phylogenetic analysis showed a low genetic variably among the isolates but allowed us to classify the viruses into different genotypes for the A and B HRSV strains.

Este trabalho teve por objetivo caracterizar e comparar a estrutura genética de sete populações de cupuaçuzeiro, Theobroma grandiflorum (Willd. ex Spreng.) Schum., uma fruteira nativa da Amazônia brasileira, utilizando marcadores microssatélites e descritores botânico-agronômicos. Visou também conhecer, preliminarmente, o sistema reprodutivo do cupuaçuzeiro. A estrutura genética das sete populações, sendo três populações naturais, coletadas na suposta área de máxima diversidade da espécie, três populações estabelecidas em Banco Ativo de Germoplasma (BAG), e uma população coletada em plantios comerciais do município de Tomé açu - PA, foi analisada com auxílio de marcadores microssatélites. Foi observada alta variabilidade genética na espécie, ressaltado pelo elevado número de alelos por loco, alto nível de heterozigosidade e divergência entre as populações. A divergência foi mais acentuada entre as populações naturais, em comparação com as populações do Banco de Germoplasma. Essa divergência pode indicar um processo preliminar de diferenciação. Porém, foi mais acentuada entre as populações oriundas de Tucuruí e Nova Ipixuna, corroborando com as indicações que consideram essa região como o centro de máxima diversidade de T. grandiflorum. Estes resultados sugerem, como estratégia de conservação in situ, a necessidade de definição de mais de um local para reserva genética, bem como, em relação a conservação ex situ, as coletas devem ser realizadas em vários locais. A elevada diversidade genética observada nos plantios comerciais, permite recomendar essas plantações como uma fonte alternativa de genes e genótipos ao programa de melhoramento de T. grandiflorum. No BAG foi observada baixa divergência genética entre as populações, sendo que, a maior parte da variabilidade genética encontrava-se dentro das populações. Essa caracterização foi complementada com o emprego de descritores botânico-agronômicos, quando foi observada grande variabilidade para a maioria dos descritores empregados. Houve necessidade, inicialmente, de selecionar dentre as 53 variáveis, aquelas que melhor se prestavam para a caracterização dos acessos. Empregando análises univariada e multivariada por componentes principais, foi possível descartar 64% das variáveis iniciais, sendo sugerida uma lista mínima de 19 descritores para o cupuaçuzeiro. Com base nessa lista e o emprego da distância Euclideana média, foi obtida uma matriz de dissimilaridade entre os 31 acessos avaliados. Esses acessos foram agrupados pelo método de Tocher e UPGMA, tendo sido obtidos seis grupos de similaridade. A comparação entre as duas caracterizações realizadas no BAG, revelou uma correlação positiva e significativa entre distâncias genéticas e fenotípicas. Preliminarmente foi estudado o sistema de reprodução do cupuaçuzeiro, numa população natural de Nova Ipixuna – PA, sendo utilizadas oito progênies de polinização aberta, com dez indivíduos e oito locos microssatélites polimórficos. Baseado na estimativa da taxa de cruzamento multilocos ( $ t m =1,0) e individual por planta materna, o estudo nessa população sugere que o T. grandiflorum é uma espécie predominantemente alógama, com uma pequena percentagem (5,4%) de cruzamentos entre parentes. Esse fator tem implicações importantes nas estratégias de conservação in situ e na utilização de progênies oriundas de polinização aberta nos programas de melhoramento. / This work had the objectives to characterize and compare the genetic structure of seven populations of cupuassu, Theobroma grandiflorum (Willd. ex Spreng.) Schum., a fruit tree native to the Brazilian Amazon using microsatellite markers and botanic-agronomic descriptors; and to investigate the cupuassu mating system. The genetic structure of seven populations of cupuassu, with three originally collected at the putative center of maximum diversity of the species; three populations established at the active germplasm collection (BAG); and one population colected from commercial plantings were analyzed using microsatellite markers. High genetic variability was observed for the species, demonstrated by the elevated number of alleles per locus; high heterozigosity and divergence between populations. The divergence was more noticeable among natural populations than among populations from the germplasm collection. This divergence might indicate a preliminary process of diversification. However, it was more pronounced between the populations from Tucuruí and Nova Ipixuna, corroborating indications that this region is considered the center of maximum diversity of T. grandiflorum. These results suggested as strategy for in situ conservation, the requirement to define more than one site for genetic reserves, large enough to maintain rare alleles in the medium- to long term. For ex situ conservation, sample collection must be conducted in many sites, with low intensity in each site, due to the existing variability witihin population. The high genetic diversity observed in commercail plantings allow to recommend these areas as an alternative source for genes and genotypes for the breeding program of T. grandiflorum. The characterization of the germplasm populations was complemented using botanic-agronomic descriptors. The large observed variability for most of the evaluated descriptors indicated that the germplasm collection contained high phenotypic diversity. Initially, it was necessary to select from the 53 evaluated variables, those most suitable for characterization of the accessions. Using univariate and multivariate analyses of principal components, it was possible to discard 64% of the initial variables, and a minimum descriptor list with 19 traits was proposed for cupuassu. Based on the minimum descriptor list, a matrix of dissimilarity was constructed using Euclidean distances. The 31 evaluated cupuassu accessions were grouped using Tocher and UPGMA, into six groups. The comparison betwen the molecular and phenotypic characterization revealed a significant and positive correlation between the genetic and phenotypic distances. The mating system fo cupuassu was studied, based on a natural population from Nova Ipixuna – PA, using eight progenies derived from open-pollinated pods with ten individuals each and eight polymorphic microsatellite loci. Based on the estimation of the multilocus outcrossing rate ( $ t m =1,0) and individual outcrossing rate ( $ t =1.0), the results from this population suggested that T. grandiflorum is a predominatly outbreeding species, with a small percentage (5,4%) of biparental inbreeding. These results have important implications on the in situ conservation strategies and on the use of open-pollinated progenies in breeding programs.

Os programas de melhoramento da cana-de-açúcar demandam aproximadamente 12 anos para a obtenção de um novo cultivar. Assim, os marcadores moleculares podem ser usados como uma ferramenta valiosa, uma vez que possibilitamo estudo da arquitetura genética de caracteres quantitativos, ajudando a reduzir este tempo. Embora a cana-de-açúcar seja uma cultura perene, para a qual o desempenho genotípico é avaliado através de ensaios estabelecidos ao longo de diferentes locais e cortes, a maior parte dos estudos de mapeamento de QTLs ignora a existência de interação entre QTLs, corte e local (QTL × H × L). Neste contexto, o presente trabalho apresenta uma estratégia que foi desenvolvida para a detecção de QTLs em cana-de-açúcar, com base em modelos mistos e mapeamento por intervalo, considerando diferentes estruturas de (co)variância que permitem supor heterogeneidade de variâncias genéticas e existência de correlações genéticas entre cortes e locais. A metodologia de modelos mistos foi aplicada aos dados de uma população segregante obtida a partir do cruzamento entre dois cultivares pré-comerciais de cana-de-açúcar, constituída por 100 indivíduos avaliados em dois locais (Piracicaba e Jaú, SP, Brasil) e em três cortes para produção (toneladas de cana por hectare, TCH), produção de açúcar (toneladas de Pol por hectare, TPH), porcentagem de fibra e Pol (teor de sacarose). A análise fenotípica resultou na seleção do modelo não-estruturado, que assume heterogeneidade de variâncias e existência de correlação genética específica para cada combinação de corte e local, para todos os caracteres avaliados. Na análise de mapeamento, foram detectados 50 QTLs, incluindo 14 QTLs para TCH, 15 para TSH, 10 para Pol e 11 para Fibra. Além disso, os resultados mostram que os efeitos das interações entre QTL e corte (QTL × H), QTL e local (QTL × L) e QTL, corte e local (QTL × H × L) foram importantes para todos os caracteres avaliados. Do total de QTLs identificados, 33 (66 %) apresentaram algum tipo de interação e apenas 17 (34 %) mostraram mesmo efeito entre as diferentes combinações de corte e local. Estes resultados fornecem informações importantes para o entendimento da base genética de caracteres quantitativos relacionados com produção e teor de sacarose em cana-de-açúcar. / Sugarcane breeding programs take at least twelve years to develop new commercial cultivars. Thus, molecular markers can be used as a valuable tool since they offer the possibility to study the genetic architecture of quantitative traits, helping to reduce this time. Although the performance of genotypes in sugarcane breeding programs has been evaluated across a range of locations and harvest years, since sugarcane is a perennial crop, many of the QTL detection methods ignore QTL by harvest by location interaction (QTL × H × L). In this work, a strategy for QTL detection in sugarcane was developed, based on mixed models and interval mapping, considering different (co)variance structures for the modeling of heterogeneous genetic variances and genetic correlations between harvests and locations. The mixed model approach was applied to a data set provided by a segregating population developed from a cross between two pre-commercial Brazilian cultivars, consisted of 100 individuals planted in two locations in 2003 (Piracicaba and Jaú, SP, Brazil) and evaluated in the first, second and third subsequent harvest years for cane yield (tonnes of cane per hectare, TCH), sugar yield (tonnes of sugar per hectare, TSH), fiber percent and Pol (sucrose content). Phenotypic analysis provided the selection of the unstructured model, which allows the assumption of heterogeneity of variance and presence of a specific genetic correlation for each combination of harvest and location. In the QTL mapping procedure, 50 QTLs were detected, including 14 QTLs for TCH, 15 for TSH, 10 for Pol and 11 for Fiber. In addition, the results show that QTL by harvest (QTL × H), QTL by location (QTL × L) and QTL by harvest by location (QTL × H × L) interaction effects were important for all evaluated traits. From the total of QTLs identified, 33 (66%) had some interaction and only 17 (34%) showed stable effects across the different combinations of harvest and location. These results can provide useful information to understand the genetic control of complex traits related with sugarcane production and sucrose content.

Os objetivos do presente trabalho compreenderam a obtenção de estimativas de parâmetros genéticos e fenotípicos, como variâncias, correlações, herdabilidades e respostas à seleção, em uma população derivada do cruzamento entre as linhagens 14 e 56 de soja, contrastantes para produção de grãos. Os tratamentos consistiram de uma amostra de 89 progênies F2:4 e 11 testemunhas comerciais, que foram avaliadas em experimentos em látice triplo 10 x 10 no ano agrícola 2007/08 na Estação Experimental Anhembi do Departamento de Genética da ESALQ/USP, localizada em Piracicaba, SP. A parcela experimental foi constituída de uma linha de 2 m de comprimento, espaçada de 0,5 m, contendo 35 plantas no estande ideal, após o desbaste. Foram avaliados os seguintes caracteres: dias até a maturação (DM), altura das plantas na maturação (AM), acamamento (AC) e produção de grãos (PG). As estimativas dos coeficientes de herdabilidade entre médias de progênies foram: elevada para AM (77,4%), mediana para DM (32,3%) e baixas para AC e PG (18,1% e 19,0%, respectivamente). Entretanto, os coeficientes de variação genética foram muito baixos para DM e AC (0,37% e 1,61%, respectivamente), e mais altos para AM e PG (6,80% e 6,83%, respectivamente), indicando a ocorrência de pouca variabilidade genética para DM e AC e, conseqüentemente, poucas perspectivas de resposta à seleção. O coeficiente de correlação genética entre AM e PG foi alto (rg = 0,67), indicando que a seleção para PG deve resultar em plantas mais altas. A estimativa da resposta com seleção das 20% progênies mais produtivas foi de 4,5%, e a resposta correlacionada em AM foi de 3,8%. Devido à baixa variabilidade genética, as respostas correlacionadas esperadas em DM e AC foram muito pequenas. Os resultados indicam que a população pode ser melhorada somente para os caracteres PG e AM. / This paper was carried out in order to estimate genetic and phenotypic parameters, such as variances, heritabilities, correlations and expected response to selection in a population derived from the cross between inbred lines 14 and 56 of soybeans, divergent for grain yield. Entries consisted of a sample of 89 F2:4 progenies and 11 commercial checks, evaluated in a triple 10 x 10 lattice design in the 2007/08 growing season at Anhembi Experimental Station of the Genetics Department (ESALQ/USP), near Piracicaba, SP. Plots were single 2-meter-long rows spaced 0.5 m apart, with 35 plants after thinning. The following traits were evaluated: days to maturity (DM), plant height at maturity (AM), lodging (AC) and grain yield (PG). Heritability estimates on a progeny mean basis were high for AM (77.4%), medium for DM (32.3%) and low for AC and PG (18.1% and 19.0%, respectively). However, genetic coefficients of variation were very low for DM and AC (0.37% and 1.61%, respectively) and higher for AM and PG (6.80% and 6.83%, respectively), which indicates low genetic variability for DM and AC and, consequently, small perspectives of response to selection. Genetic correlation coefficient between AM and PG was high (rg = 0.67), indicating that selection for higher PG will result in taller plants. Expected response based on selection of the 20% high yielding progenies was 4.5%, and the correlated response in AM was 3.8%. The correlated response in DM and AC were very low, due to the low genetic variability. General results have shown that the population can be improved only for the traits PG and AM.

Abstract Many waders are in decline, and the number of endangered species and populations is increasing. Their protection and management requires knowledge of both ecological and genetic state of the populations. In this thesis, I studied the distribution-wide genetic variation, structure and phylogeography of the Temminck’s Stint (Calidris temminckii) and Terek Sandpiper (Xenus cinereus) using microsatellites and sequence data from the mitochondrial control region and cytochrome oxidase I gene. I compared these regionally endangered species to other waders with varying evolutionary histories, breeding systems and habitat preferences to examine the levels of genetic variation and structure at different spatial scales. In addition, I studied the genetic structure of the endangered Baltic population of the Southern Dunlin (Calidris alpina schinzii) with microsatellites. I used genetic information in all three study species to determine units for conservation. The Temminck’s Stint and Terek Sandpiper, both not restricted to the Arctic, had low distribution-wide structuring. They also had quite low levels of variation when compared to other species breeding at similar latitudes, indicating reductions in population sizes during past climate changes. Especially the peripheral breeding populations were differentiated and showed signs of inbreeding and genetic drift when compared to the main range. The Temminck’s Stint populations at the Bothnian Bay and Yakutia, and Terek Sandpiper populations in Finland and Belarus, should be treated as separate management units. The broader interspecific comparison of waders suggests that habitat availability, mating system and the extent of philopatry may affect the genetic composition of species. The genetic analyses of the Southern Dunlin indicated strong effects of philopatry and inbreeding throughout the range. Local subpopulations at the Bothnian Bay and in Sweden need to be considered as separate management units. Management efforts at the Baltic should be focused on increasing connectivity and providing large enough breeding habitats for potential immigrants and recruits. / Tiivistelmä Useat kahlaajapopulaatiot ovat pienentyneet ja uhanalaistuneet maailmanlaajuisesti. Lajien ja populaatioiden ekologiaa ja genetiikkaa on tunnettava, jotta suojelutoimia voidaan kohdistaa oikein. Tutkin väitöskirjassani lapinsirrin (Calidris temminckii) ja rantakurvin (Xenus cinereus) geneettistä rakennetta, muuntelua ja fylogeografiaa levinneisyysalueen laajuisesti mikrosatelliittien ja mitokondrion kontrollialueen ja sytokromioksidaasi I -geenin sekvenssien avulla. Tutkin, mitkä tekijät vaikuttavat geneettisen rakenteeseen ja muunteluun vertaamalla näitä lajeja muihin kahlaajiin, joilla on erilaisia lisääntymisstrategioita, jotka pesivät vaihtelevissa ympäristöissä ja joista monet eroavat toisistaan myös fylogeografialtaan. Lisäksi tutkin Itämeren rannalla pesivän etelänsuosirrin (Calidris alpina schinzii) geneettistä populaatiorakennetta mikrosatelliittien avulla. Käytin geneettistä tietoa hyväksi luonnonsuojeluyksikköjen määrittämisessä kaikille kolmelle tutkimuslajilleni. Lapinsirrin ja rantakurvin fylogeografinen historia oli samankaltainen. Geneettisen muuntelun määrä oli vähäisempää verrattuna muihin, samankaltaisissa ympäristöissä pesiviin kahlaajiin. Molemmat lajit ovat todennäköisesti kärsineet historiallisten ilmaston-muutosten aiheuttamasta populaatioiden pienenemisestä. Erityisesti levinneisyysalueen reunoilla pesivät populaatiot olivat erilaistuneita, ja niissä näkyi sukusiitoksen ja geneettisen satunnaisajautumisen merkkejä. Perämeren ja Jakutian lapinsirri- sekä Valko-Venäjän ja Suomen rantakurvipopulaatioita tulee kohdella erillisinä suojeluyksiköinään. Vertailu muihin kahlaajiin osoitti, että niin pesimä- ja talvehtimisalueiden laajuus kuin lisääntymisstrategiat ja paikkauskollisuus voivat vaikuttaa lajien geneettiseen koostumukseen. Etelänsuosirrin geneettiset analyysit paljastivat merkkejä sukusiitoksesta, joita paikkauskollisuus ja populaatioiden pienuus ovat voimistaneet. Perämeren ja Ruotsin populaatioita tulee kohdella erillisinä suojeluyksiköinään. Suojelutoimet on kohdistettava tarpeeksi suurien, hyvälaatuisten pesimäpaikkaverkostojen ylläpitämiseen.