Kakapo (Strigops habroptilus) are a flightless, nocturnal parrot endemic to New Zealand. Thought to be extinct within their natural range, kakapo are currently listed as nationally critical. The current population of 86 individuals is managed by the Department of Conservation’s National Kakapo Team on two offshore islands in southern New Zealand, with all females of breeding age on Codfish Island (Whenua Hou). Kakapo only breed once every two to five years, coinciding with the mast fruiting of specific plant species. On Codfish Island, the proportion of adult female kakapo that breed in rimu (Dacrydium cupressinum) fruiting years is dependent on the quantity of fruit produced, with fewer females attempting to breed during low mast years. The purpose of this research is to investigate why only some adult female kakapo breed in low rimu fruiting years on Codfish Island, specifically assessing if foraging home range size and/or habitat selection influence breeding. A total of 506 location points were collected at night for 18 adult female kakapo between March and May 2006. These were used to estimate foraging home ranges and to assess if kakapo select for particular types of vegetation. Ecological Niche Factor Analysis was used to determine the relative importance of habitat variables in the distribution of female kakapo and to predict areas of suitable breeding habitat when rimu fruit is limited. The breeding success of individuals in 2005, a low rimu mast year, was used to identify if differences in home ranges or habitat selection occurred between breeding and non-breeding females. The large variation in foraging home range sizes recorded in this research was consistent with previous studies. Foraging home range sizes were on average twice the size for breeders than for non-breeders, suggesting that adult female kakapo may be limited in their ability to breed by the size of the area they occupy. Adult female kakapo did not randomly use vegetation on Codfish Island as some vegetation types were not used, while others were common inside foraging home ranges. Adult female kakapo utilise a broad niche and are capable of surviving in a wide range of habitats. However, breeding females were more specialised in their niche requirements than non-breeders, with breeders utilising areas with higher abundances of mature rimu trees. Females occurred in high elevation, flat areas of the island but this may have been because this is where appropriate vegetation types occurred. During low rimu mast years, breeding adult females were predicted to occupy habitat in high elevation, plateau areas with a high abundance of rimu. Areas identified as sub-optimal habitat for breeding included the coastal areas, the lower elevation area of the main valley and some ridgelines. The home ranges of all 10 breeding females contained some optimal habitat, while females who did not breed were more likely to be located in sub-optimal habitat. Although there were significant areas of optimal breeding habitat not occupied by adult female kakapo, other kakapo may have been present in these areas. To increase the proportion of females that breed in low rimu mast years, it may be necessary to remove sub-adult females or surplus adult males living in optimal breeding habitat from the island. Alternatively, females in sub-optimal breeding habitat could be fed supplementary foods or transferred to other islands where there is unoccupied suitable breeding habitat available.

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Climate change predictions suggest that the continent most vulnerable to climate change is Africa. The impacts of potential changes which include increases in air temperatures and rainfall variability are negative with potential species extinctions projected throughout southern Africa. A number of climate models have been applied to examine the consequences of climate change for ranges of South African animal species. One such model frequently predicted range shifts from west to east, which is realistic considering the marked aridity gradient in an east-west direction across the country, but the authors suggested that these shifts may not be as marked if species are able to use physiological and behavioural methods to adapt to an increase in aridity. Information on the degree to which behavioural and physiological flexibility affect species range in southern Africa is scant which is surprising given its importance with regard to climate change. Thallomys nigricauda occurs along an east-west aridity gradient in southern Africa, inhabiting mesic, semi-xeric and xeric regions. One would expect phenotypic flexibility in physiological and behavioural traits in response to the diverse environmental conditions to be related to the success and range of the species. The wide distribution and arboreal habits, suggesting that T. nigricauda is exposed to greater extremes of temperature than fossorial rodents, makes T. nigricauda an ideal species to test this assumption. Hence I expected that T. nigricauda would exhibit variation in physiological and behavioural traits measured along an aridity gradient. This has important implications in predicting the survival of small mammal species in the light of climate change in southern Africa. Thallomys nigricauda were live-trapped in winter 2006 and 2007 and summer 2007 using Elliot traps in three sites: mesic site Weenen Game Reserve (KwaZuluiv Natal Province, South Africa); semi-xeric site Haina Game Farm (Botswana) on the northern boundary of the Central Kalahari Desert and xeric site Molopo Nature Reserve (southern Kalahari savannah, North-West Province, South Africa). I studied the home-range size of T. nigricauda by radiotracking 12 males and 16 females in winter 2006, 2007 and summer 2007. Home ranges were estimated using 100% and 95% minimum convex polygons and 95% and 50% fixed kernels. Home ranges varied widely, from 166 to 80199m2 for males and from 46 to 8810m2 for females. Males had larger home ranges than females, which supports a promiscuous mating system reported for the species. Although range size was reduced in both sexes in winter, this was not significant. I found no significant difference in home range size along the aridity gradient. It is suggested that a combination of precipitation, habitat productivity and breeding system influences the size of home range of the species, and that this species displays phenotypic flexibility in terms of its behavioural responses to these factors. I measured the urine concentrating ability (UCA), as indicated by urine osmolality and relative medullary thickness (RMT), and water turnover rate (WTR) of T. nigricauda. There was no significant difference in RMT between sites or sex and no difference in osmolalities when site, season and sex were taken into account. In addition, specific WTR was not significantly influenced by season. Lack of significant differences could be the result of the high degree of individual variation in the traits measured, an indication of the flexibility in UCA and WTR. However, higher urine osmolality and lower WTR’s were recorded in the dry winter months. I quantified the thermal environment perceived by a small, arboreal, mammalian endotherm using a number of methods at three study sites in winter and summer. Our area of interest was how well these methods accurately portrayed the actual temperatures that small mammals are exposed to. Temperature differences between the methods were largest during the midday, when temperatures were highest. All methods recorded a greater range of temperatures during photophase than during scotophase. Black-bulb and model temperatures produced more accurate, rapid measurements when compared to measurements produced by direct temperature recording devices, particularly during photophase, when solar radiation is the major influence of heating. Other methods lagged behind black-bulb measurements. Although the mean temperatures of some of the methods were significantly different, there was a high degree of correlation between all methods, even after randomization and generation of 25% and 10% subsamples. Computed thermal indices and blackbulb temperatures produced similar thermal profiles. In studies requiring accurate time series measurements, it is suggested that black-bulb or copper models be employed rather than direct temperature recording devices. Simpler measurement devices would suffice for studies requiring an estimate of the temperature variation and trends in the microclimate of small mammalian endotherms, particularly arboreal or cavity dwelling species. In the wild, across an aridity gradient, I measured abdominal body temperarture (Tb) of T. nigricauda using implanted iButtons®. All but three T. nigricauda displayed significant 24 h Tb rhythmicity. The Tb range for free-living T. nigricauda was 32.33-40.63 oC (n = 13) and 32.69-40.15 oC (n = 17) in winter and summer respectively. Although there was variation in Tb profiles, T. nigricauda generally displayed a bimodal distribution of Tb, with high and low Tb values during scotophase and photopase respectively. Body temperature range was significantly greater in winter, when T. nigricauda reduced its minimum Tb. It was shown that the maximum amplitude of circadian rhythms of body temperature was on average 259.6% of expected values. To determine the extent to which the microclimate of T. nigricauda cavities assists in the maintenance of Tb, I measured the temperatures of cavities across the gradient, providing an indication of the degree of buffering provided by refugia. I measured the temperatures of shallow and deep regions of cavities using iButtons® in summer and winter and recorded operative and shade temperatures for comparison. Compared with operative temperature, cavities had stable microclimates, displaying smaller ranges in temperature. Mean minimum and maximum cavity temperatures differed significantly to operative temperature and between seasons, whereas there was no significant difference between shallow and deep measurements in cavities. Differences in the buffering capacities of the cavities between seasons were not significant. To determine whether T. nigricauda alter its length of exposure in response to lower ambient temperatures in winter as a means of maintaining Tb, I measured the activity of T. nigricauda, defined as the proportion of fixes outside the home cavity of the individual. Males spent a greater proportion of the active phase away from their home cavity in summer, and significantly in winter when compared with females, but there were no differences between seasons. It is suggested that T. nigricauda realize energy savings by lowering its Tb during their rest phase during the day, allowing them to maintain nocturnal activity and overall energy balance. Thus, besides the larger male home range, a result of the reproductive pattern, the physiological and behavioural traits of T. nigricauda measured in this study did not differ between aridity sites or seasons. The results of this study, in highlighting the variation in physiological and behavioural responses of subpopulations of T. nigricauda to diverse conditions, suggest that this variation is due to phenotypic flexibility. Understanding the extent and nature of this flexibility is critical to our comprehension of the consequences climate change. By defining the presence and extent of intraspecific variation in physiology and behaviour, this study resolved the necessary first step towards this understanding for the widely distributed T. nigricauda in southern Africa. / Thesis (Ph.D.)-University of KwaZulu-Natal, Pietermaritzburg, 2008.

Past research suggests that social organisation in Australian rodent species is determined by the predictability of resources in the environment (Happold 1976a). Notomys alexis (the spinifex hopping mouse or tarrkawarra) is widely distributed throughout the Australian arid-zone (Breed 1998a; Watts & Aslin 1981). Large groups of animals have been found sharing burrows in the wild and laboratory observations suggest that the species is highly social (Happold 1976a; Stanley 1971). A closely related species, Notomys mitchelli (Mitchell’s hopping mouse or pankot) is relatively common throughout the southern semi-arid zone (Watts 1998a; Watts & Aslin 1981). Much less is known about N. mitchelli; field studies have been subject to low recapture rates and few laboratory studies have involved this species (Baverstock 1979; Cockburn 1981a; Crichton 1974). Following Happold (1976a), it was hypothesised that the socio-ecology of N. mitchelli will be qualitatively different to that of N. alexis. Studying wild populations of Notomys mitchelli in the Middleback Ranges, South Australia and N. alexis outside the desert township of Roxby Downs, S.A., this research aimed to describe the socio-ecology of these species, with reference to the predictability of their environments. Uniquely, bioclimatic modelling of the species’ known distributions was also conducted to confirm that the study’s underlying assumption that the two rodents inhabit essentially different environments was correct. These studies were complemented by the observation of captive groups of N. alexis. This work confirmed that the habitats of Notomys mitchelli and N. alexis are distinct; the more arid habitat of N. alexis is subject to greater environmental fluctuations than that of the semi-arid dwelling N. mitchelli. Contrary to expectations, however, observation of free-living animals characterised N. mitchelli social groups as highly unstable; while particular individuals remained in the population for long periods, many animals appeared to be transients. Further, burrow groups appeared to be much smaller than predicted by Happold (1976a), and based on loose aggregations of male animals rather than small groups of females. While decidedly social in the laboratory, free-living N. alexis lived in groups no bigger than N. mitchelli and these groups were equally ephemeral in constitution. Moreover, free-living N. alexis appeared to utilise activity areas that were no larger than those used by N. mitchelli, despite occupying a more unpredictable and apparently less well-resourced habitat. As a whole, this research represents a comprehensive examination of the principal behavioural theory commonly applied to Australian native rodent species, untested since its publication three decades ago. From the data collected during this work, it cannot be said that the environmental predictability hypothesis for native rodent social organisations as proposed by Happold (1976a) is adequate to differentiate the social behaviour of these semi-arid and arid-dwelling species. Instead, it is suggested that, while both N. mitchelli and N. alexis are undoubtedly socially tolerant, predation and/or parasite load, driving burrowing behaviour, has a greater influence on the social behaviour of free-living rodent populations than habitat predictability. / http://proxy.library.adelaide.edu.au/login?url= http://library.adelaide.edu.au/cgi-bin/Pwebrecon.cgi?BBID=1373743 / Thesis (Ph.D.) - University of Adelaide, School of Earth and Environmental Sciences, 2009

Past research suggests that social organisation in Australian rodent species is determined by the predictability of resources in the environment (Happold 1976a). Notomys alexis (the spinifex hopping mouse or tarrkawarra) is widely distributed throughout the Australian arid-zone (Breed 1998a; Watts & Aslin 1981). Large groups of animals have been found sharing burrows in the wild and laboratory observations suggest that the species is highly social (Happold 1976a; Stanley 1971). A closely related species, Notomys mitchelli (Mitchell’s hopping mouse or pankot) is relatively common throughout the southern semi-arid zone (Watts 1998a; Watts & Aslin 1981). Much less is known about N. mitchelli; field studies have been subject to low recapture rates and few laboratory studies have involved this species (Baverstock 1979; Cockburn 1981a; Crichton 1974). Following Happold (1976a), it was hypothesised that the socio-ecology of N. mitchelli will be qualitatively different to that of N. alexis. Studying wild populations of Notomys mitchelli in the Middleback Ranges, South Australia and N. alexis outside the desert township of Roxby Downs, S.A., this research aimed to describe the socio-ecology of these species, with reference to the predictability of their environments. Uniquely, bioclimatic modelling of the species’ known distributions was also conducted to confirm that the study’s underlying assumption that the two rodents inhabit essentially different environments was correct. These studies were complemented by the observation of captive groups of N. alexis. This work confirmed that the habitats of Notomys mitchelli and N. alexis are distinct; the more arid habitat of N. alexis is subject to greater environmental fluctuations than that of the semi-arid dwelling N. mitchelli. Contrary to expectations, however, observation of free-living animals characterised N. mitchelli social groups as highly unstable; while particular individuals remained in the population for long periods, many animals appeared to be transients. Further, burrow groups appeared to be much smaller than predicted by Happold (1976a), and based on loose aggregations of male animals rather than small groups of females. While decidedly social in the laboratory, free-living N. alexis lived in groups no bigger than N. mitchelli and these groups were equally ephemeral in constitution. Moreover, free-living N. alexis appeared to utilise activity areas that were no larger than those used by N. mitchelli, despite occupying a more unpredictable and apparently less well-resourced habitat. As a whole, this research represents a comprehensive examination of the principal behavioural theory commonly applied to Australian native rodent species, untested since its publication three decades ago. From the data collected during this work, it cannot be said that the environmental predictability hypothesis for native rodent social organisations as proposed by Happold (1976a) is adequate to differentiate the social behaviour of these semi-arid and arid-dwelling species. Instead, it is suggested that, while both N. mitchelli and N. alexis are undoubtedly socially tolerant, predation and/or parasite load, driving burrowing behaviour, has a greater influence on the social behaviour of free-living rodent populations than habitat predictability. / http://proxy.library.adelaide.edu.au/login?url= http://library.adelaide.edu.au/cgi-bin/Pwebrecon.cgi?BBID=1373743 / Thesis (Ph.D.) - University of Adelaide, School of Earth and Environmental Sciences, 2009

Les patrons récursifs de déplacement, où l’individu revient à des sites déjà visités, sont très répandus. L’utilisation de la mémoire, supposée être avantageuse lorsque l’environnement est prévisible, pourrait être sous-jacente à l’émergence de ces patrons. Cependant, notre compréhension de l’interface mémoire-déplacement a jusqu'à présent été limitée par un manque de méthodes adaptées et d’investigation théorique des avantages de l’utilisation de la mémoire et des patrons qui en émergent. Au cours de cette thèse j’ai cherché à combler en partie ces manques. Je propose ici trois nouveaux cadres d'analyse des patrons récursifs de déplacement. Le premier délimite les zones les plus fréquemment revisitées par un individu, le deuxième détecte la périodicité dans les revisites de sites connus, et le troisième définit formellement et quantifie la routine de déplacement en termes de répétitivité de la séquence de déplacement, et propose un algorithme pour détecter les sous-séquences répétées. A l'aide d'un modèle individu-centré, nous montrons que l'utilisation de la mémoire dans un environnement prévisible est très avantageuse énergétiquement comparée à une stratégie de recherche sans mémoire, y compris en situation de compétition, et qu'elle mène à l'émergence de domaines vitaux stables et à la ségrégation spatiale entre individus. L'utilisation de la mémoire invalide plusieurs hypothèses très courantes faites par les études populationnelles, en menant à une forte déplétion de l’environnement, à une augmentation de la taille de la population à l’équilibre, et à une relation non linéaire entre la taille de population totale et l’intensité de compétition localement ressentie par les individus. Ainsi, ma thèse contribue à une meilleure compréhension des conséquences de la mémoire sur la valeur sélective des individus, sur les patrons de déplacement, et sur la démographie des populations. Elle propose des méthodes innovantes pour quantifier et caractériser les patrons récursifs de déplacement pouvant émerger de son utilisation. Ces méthodes devraient ouvrir de nouvelles opportunités de comparaisons entre individus de différentes populations ou espèces qui permettront le test d'hypothèses sur les pressions de sélection favorisant l'utilisation de la mémoire. / Recursive movement patterns, by which an individual returns to already visited sites, are very common. Memory use, hypothesized to be advantageous when the environment is predictable, could underlie the emergence of these patterns. However, our understanding of the memory-movement interface has been limited by two knowledge gaps. We still lack appropriate methodologies and theoretical knowledge of the advantages of memory use and of the patterns that emerge from it. During this PhD project, I aimed at filling in some of these gaps. I present here three new frameworks for the analysis of recursive movement patterns. The first one delimits the areas most frequently revisited by an individual, the second one detects periodic revisit patterns, and the third one formally defines and quantifies routine movement behaviour in terms of movement sequence repetitiveness, and presents an algorithm that detects the sub-sequences that are repeated. Using an individual-based model, we show that memory use, when the environment is predictable, is very energetically advantageous compared to foraging strategies that do not use memory, including in a situation of competition, and that it leads to the emergence of stable Home Ranges and spatial segregation between individuals. Memory use invalidates several hypotheses very commonly made in population studies, by leading to a stronger environmental depletion, to a higher equilibrium population size, and to a nonlinear relationship between the total population size and the individually-experienced intensity of competition. Therefore, my PhD thesis contributes to a better understanding of the consequences of memory use for the fitness of individuals, for movement patterns, and for population dynamics. It offers innovative methodologies that quantify and characterize recursive movement patterns that can emerge from its use. These methods should open new opportunities for the comparison of the movements of individuals from different populations and species, and thus the testing of hypotheses about the pressures that select for memory use.

O comportamento territorial é exibido por animais que competem por recursos dentro de uma área específica defendida. Ao excluir competidores potenciais desta área através de comportamentos agressivos, os indivíduos territoriais garantem acesso prioritário aos recursos essenciais para sua sobrevivência e reprodução. Em anfíbios anuros, a territorialidade tem sido relacionada principalmente com espécies de reprodução prolongada, cujos sítios reprodutivos estão disponíveis durante todo o ano. O presente trabalho foi realizado em um trecho de riacho na Floresta da Tijuca, Rio de Janeiro. Foram realizadas quatro visitas consecutivas a área de amostragem em cada mês (abril/2009 à agosto/2010). O objetivo foi responder questões sobre a territorialidade dos indivíduos da espécie Hylodes nasus: (área de vida, fidelidade ao sítio, comportamentos agonísticos e combates físicos). As áreas de vida dos machos apresentaram relação significativa com o número de recapturas. O tamanho da área de vida das fêmeas foi ligeiramente maior do que dos machos. Os machos apresentaram maior fidelidade do que as fêmeas. A fidelidade apresentou resultado significativo com o CRC e a massa corporal dos indivíduos. Foram observadas 50 interações agonísticas entre machos, sendo exibidos 11 comportamentos agressivos. Foram observados 19 combates físicos, sendo os machos envolvidos classificados como residente, intruso, vencedor ou perdedor. Todas as disputas foram vencidas por indivíduos residentes. Informações a respeito da influência de fatores ambientais sobre a população de H. nasus, aspectos da estrutura populacional e descrição do microhábitat também são fornecidos. / The territorial behavior is exhibited by animals that compete for resources within a specific defended area. By excluding potential competitors in this area through aggressive behavior, territorialist individuals ensure priority access to essential resources for their survival and reproduction. In anuran amphibians, territoriality has been mainly related to prolonged-breeding species, whose breeding sites are available throughout the year. This study was conducted in a portion of the river in the Tijuca Forest, Rio de Janeiro. There were four consecutive visits to the sampling area in each month (April/2009 to August/2010). The objective was to answer questions about the territorial behavior of Hylodes nasus (home range, site fidelity, agonistic behaviors and physical fighting). The males home range showed a significant relation with number of recapture. The home range estimated for females was slightly larger than males. Males have higher site fidelity than females. The site fidelity showed a significant relation with individuals' SVL and body mass. There were observed 50 agonistic encounters between males, showing 11 aggressive behaviors. There were observed 19 physical fights with males being classified as resident, intruder, winner or loser. All contests were won by resident individuals. Information about the influence of environmental factors on the population of H. nasus, aspects of population structure and description of microhabitat are also provided.

Comprometida com a compreensão da relação entre hábitat e uso do espaço pelo mico-leão-da-cara-preta (Leontopithecus caissara), esta dissertação se norteia por três perguntas: Diferenças de hábitat entre ilha e continente influenciam o tamanho da área de vida? Há predileção da espécie por alguma classe de vegetação dentro da área de uso? Qual a capacidade suporte em sua área de ocorrência continental, bem como nas áreas potenciais para seu manejo conservacionista? Na tentativa de elucidar essas questões esta dissertação se divide em três capítulos. O primeiro contextualiza o trabalho e a apresenta o estado atual de conhecimento de L. caissara. Os capítulos segundo e terceiro concernem às questões centrais do trabalho - uso e seleção do hábitat pelo mico-leão-da-cara-preta. No capítulo dois apresentamos o uso do espaço pela espécie em sua região continental de ocorrência e comparamos os resultados obtidos com as informações disponíveis para a Ilha do Superagui. No capítulo três tratamos da seleção do hábitat por grupos insulares e continentais de L. caissara e estimamos a capacidade suporte para a espécie considerando seus limites de ocorrência e as áreas passíveis de receber animais em situação de manejo. Ao final desses capítulos apresentamos algumas considerações e recomendações para pesquisa e conservação do mico-leão-da-cara-preta. A preocupação com uma postura crítica e construtiva acerca das metodologias de estudos e análises sobre uso do espaço por espécies animais é transversal aos assuntos tratados ao longo de todo o trabalho. Os resultados apresentados confirmam as grandes áreas de vida de L. caissara, as quais parecem ser compensadas energeticamente pela incorporação de novas áreas e abandono de outras ao longo do tempo. Os tipos de hábitats mais intensamente utilizadas pelos mico-leão-da-cara-preta intercalaram áreas de floresta madura e em clímax edáfico com áreas antropizadas em sucessão, ambos hábitats sobre pouco desnível altimétrico. A capacidade suporte estimada é aparentemente incapaz de sustentar uma população viável e ressalta a urgência de pesquisas genéticas que colaborem para a compreensão do histórico ecológico/evolutivo de L. caissara. Potenciais translocações com vistas ao aumento populacional devem considerar as amplas áreas de diva, a espacialidade dinâmica, a relação uso/disponibilidade do hábitat e as diferenças entre ilha e continente. / This dissertation focuses on the interaction between habitat and space use by the black-faced lion tamarin (Leontopithecus caissara). We seek to answer three questions: 1) Do differences in vegetation between insular and continental habitats influence how the species use the space? 2) Does the species prefer a specific type of vegetation within its home-range? 3) What is the carrying capacity of the continental distribution and which are areas for potential conservation management? The first chapter of this dissertation relates the subjects discussed and introduces what is known about L. caissara. The second and third chapters develop the central questions of the research: the use and selection of habitat by the black-faced lion tamarin. In Chapter Two, we introduce space use by the species in its continental distribution and compare the results with data from Superagui Island. In Chapter Three, we address habitat selection by insular and continental groups of L. caissara and estimate the carrying capacity for the species given its distribution and areas potentially able to receive animals in a management context. The conclusion of each chapter presents considerations and recommendations for research and conservation. The study methods and analyses of space use aim to be critical and constructive and are relevant to the topics addressed throughout the text. The results presented confirm that the large home-ranges of L. caissara undergo dynamic turnovers, with some areas being abandoned and others incorporated throughout the year. The habitat types most intensively used by tamarins include areas of mature and forest mixed with areas of anthropic succession, both occurring at low altitudes. The estimated carrying capacity is apparently insufficient to maintain a viable population and highlights the importance of genetic studies that incorporate the ecological/evolutionary history of the species. Potential translocations meant to increase population size should consider the large home-ranges, dynamic spatial structure, relation of habitat use/availability and the differences between island and continent.

As aves de rapina, assim como os outros grupos animais, não estão distribuídas de maneira uniforme nos diferentes hábitats que compõem a paisagem terrestre. Conhecer e entender os fatores (e as implicações) que levam as espécies a escolher um determinado hábitat é questão essencial nos estudos de ecologia. Esse tema ganha ainda mais importância não só pela escassez de informações sobre a ecologia e história natural das aves de rapina na região Neotropical, mas também, pelo atual cenário de alteração dos hábitats. Estes são modificados rapidamente sem que haja um conhecimento básico da relação espécie/hábitat e dos efeitos provocadas por tais alterações. Dessa maneira, a presente tese teve como objetivo principal verificar o uso e a seleção de hábitat por aves de rapina diurnas em uma paisagem heterogênea (151. 866 ha) na região central do Estado de São Paulo (22° 15′ S; 47° 49′ W), onde a Estação Ecológica de Itirapina (EEI) foi considerada como área núcleo. Ainda, foi também alvo desse estudo estimar a área de vida de três espécies de rapineiros (Falco femoralis, Rupornis magnirostris e Heterospizias meridionalis) por meio de rádio-telemetria; verificar a eficiência de captura das aves de rapina frente a dois tipos de armadilhas, bal-chatri e goshawk; e elaborar um mapa de uso/ocupação do solo da área em questão, bem como analisar a paisagem no entorno da EEI. Entre setembro de 2005 e fevereiro de 2007 foram registradas 19 espécies de Falconiformes (Pandionidae n =1, Falconidae n = 5, Accipitridae n = 13) em uma paisagem essencialmente ocupada por monoculturas (cana-de-açúcar 22 %, laranja 14 %, eucalipto 13 %) e pastagens (21%). A riqueza média dos Falconiformes em áreas de monoculturas foi de 4,6 espécies e nas áreas naturais 10,3. A composição de espécies da taxocenose se mostrou mais relacionada às outras de área abertas sob influência do Cerrado. Um total de 48 indivíduos, pertencentes a cinco espécies, foram capturados pelos dois tipos de armadilhas. O sucesso de captura geral foi de 15,3 % (n = 33) para a armadilha bal-chatri e de 1 captura a cada 11,8 dias (8,5 %) para goshawk trap (n = 15). Implicações e limitações referentes à captura das aves de rapinas em áreas abertas foram também discutidas. A média da área de vida pelo método Kernel adaptativo (KA) 95 % foi de 1.329 ± 780 ha para F. femoralis, 129 ± 140 ha para R. magnirostris e de 1.883 ha para o indivíduo de H. meridionalis. A média da área de vida de F. femoralis foi 2,8 maior em áreas alteradas quando comparada a áreas naturais. De maneira geral, a qualidade do hábitat parece ter influenciado nos diferentes valores de requerimento de área apresentado pelos indivíduos e, também, na seleção/rejeição dos diferentes hábitats. Na maioria dos casos, as monoculturas foram rejeitadas, enquanto as áreas naturais foram selecionadas pelas aves de rapina. Cana-de-açúcar foi rejeitada por todas as aves de rapina. O único ambiente alterado utilizado em maior proporção que o esperado foi pastagem, selecionada por quatro das 10 espécies analisadas. Em contrapartida, três espécies evitaram este hábitat. Este é o primeiro estudo a avaliar a seleção de hábitat por Falconiformes no Brasil e demonstra que o intensivo incremento de áreas para agricultura pode afetar negativamente até mesmo as espécies mais abundantes e generalistas, contrário a algumas generalizações da literatura. A interação entre estrutura do hábitat, disponibilidade de presas, morfologia e comportamento de caça parece explicar tanto o tamanho da área de vida requerida quanto a utilização diferenciada dos diferentes tipos de hábitats. / Raptors, similarly to other animal groups, are not randomly distributed in the different habitats in the terrestrial landscape. Knowing and understanding the factors (and implications) influencing these species to chose a certain habitat are essential in ecological studies. This subject has become even more important not only because of the lack of information on the ecology and natural history of raptors of the Neotropics, but also because of current scenario of habitat changes. Areas are being rapidly modified without a basic knowledge of the species/habitat relationship and the effects it may cause. Thus, the main goal of this thesis was to examine habitat use and selection by diurnal birds of prey in a heterogeneous landscape (151. 866 ha) in the central region of state of São Paulo (22° 15′ S; 47° 49′ W), where the Estação Ecológica de Itirapina (EEI) was considered the central area. Also, this study aimed at estimating the home range size of three raptor species (Falco femoralis, Rupornis magnirostris and Heterospizias meridionalis) through radio-telemetry; examining the efficiency of capture of birds of prey using two types of traps, bal-chatri and goshawk; and mapping land use/occupation of the study area and making the landscape analysis around the EEI. Between September 2005 and February 2007, 19 species of Falconiformes (Pandionidae n = 1, Falconidae n = 5, Accipitridae n = 13) were observed in a landscape basically occupied by monocultures (sugar cane 22 %, orange 14 %, eucalyptus 13 %) and pastures (2 1%). The average richness of Falconiformes in areas occupied by a monoculture was 4,6 species and 10,3 in natural areas. The species composition of the assemblage was more similar to those of other open areas influenced by Cerrado. Forty-eight individuals from five species were captured in the two types of traps. The general capture success was 15.3 % (n = 33) for the bal-chatri trap and 1 capture every 11,8 days (8,5 %) for the goshawk trap (n = 15). Implications and limitations of the capture of birds of preys in the areas were also discussed. The average home range obtained with the 95 % adaptive Kernel method (AK 95%) was 1.329 ± 780 ha for F. femoralis, 129 ± 140 ha for R. magnirostris and 1.883 ha for the individual of H. meridionalis. The average home range of F. femoralis was 2.8 higher in altered areas when compared to natural ones. In general, habitat quality seems to have influenced the different values of home range requirement of individuals, and also, in the selection/rejection of the different habitats. In most cases, monocultures were rejected, while natural areas were selected by raptors. Sugar cane plantations were rejected by all raptors. The only altered habitat used more than expected was pastures, selected by four of ten species analyzed. However, three species avoided this habitat. This is the first study to evaluate habitat selection by Falconiformes in Brazil and demonstrate that the increase of areas for agriculture may negatively affect even the most abundant and generalist species, contrary to some generalizations described in the literature. The interaction among the habitat structure, prey availability, morphology and hunting behavior seems to explain home range size requirements as well as the differential use of the various types of habitats.

Informações sobre o tamanho da área de vida, o uso e seleção de habitat contribuem para o entendimento da ecologia das espécies e por isso acabam servindo como importantes referências para o manejo e conservação. Apesar de no Hemisfério Norte muitos estudos abordarem área de vida e uso de habitat em Strigiformes, na região Neotropical, informações dessa natureza ainda são escassas na literatura. No presente estudo, quatro indivíduos machos da corujinha-do-mato (Megascops choliba) foram monitorados por radiotelemetria durante cerca de seis meses em uma área de cerrado (lato sensu) no interior do Estado de São Paulo. Apesar das diferenças dos habitats utilizados, o tamanho médio da área de vida de M. choliba segundo o mínimo polígono convexo (51,2 ± 26,9 ha) foi semelhante à de espécies do mesmo gênero na América do Norte. A grande variação individual encontrada no tamanho das áreas de vida pode ser explicada pelos tipos de habitats utilizados e também pelo status social dos indivíduos. No período noturno, a corujinha-do-mato preferiu fisionomias de cerrado semi-abertas e fechadas e, além disso evitou fisionomias abertas. No período diurno, habitats com vegetação mais densa e fechada como matas de galeria e manchas de Pinus invasor foram preferencialmente utilizados para uso como abrigo. O uso desses locais durante o dia, provavelmente está ligado à maior cobertura vegetal dessas áreas que podem fornecer proteção contra predadores e também microclimas adequados. / Information on home ranges and habitat use and selection is useful to understand species ecology and therefore may help to establish species management and conservation plans. Despite the large numbers of Northern Hemisphere studies addressing Strigiformes home range and habitat use, the same is not applied to Neotropical owl species, what makes such information still scarce. In this study, four males of Tropical Screech-Owls (Megascops choliba) were radio-tracked for about six months in a cerrado (lato sensu) region in state of São Paulo, southeastern Brazil. Despite the differences in used habitats between species from the two hemispheres, the mean home range size of Tropical Screech-Owls (51.2 ± 26.9 ha) appears to be similar to North American Megascops species. The considerable individual variation in home range sizes may be related to types of habitats and individual social status. At night, the Tropical Screech-Owls preferred semi-open and closed savannas and, moreover, avoided open savannas. Habitats with dense vegetation, such as gallery forests and invasive pine forests were preferentially used for daytime roost. Use of these sites during the day is probably associated to higher vegetation cover which can provide protection against predators and suitable microclimates