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  • About
  • The Global ETD Search service is a free service for researchers to find electronic theses and dissertations. This service is provided by the Networked Digital Library of Theses and Dissertations.
    Our metadata is collected from universities around the world. If you manage a university/consortium/country archive and want to be added, details can be found on the NDLTD website.
1

Predator-prey interactions of raptors in an arctic environment

Nyström, Jesper January 2004 (has links)
<p>This thesis concerns the predator-prey interactions of three raptor species in a Swedish arctic community: the gyrfalcon (<i>Falco rusticolus</i>), the rough-legged buzzard (<i>Buteo lagopus</i>) and the golden eagle (<i>Aquila chrysaetos</i>).</p><p>The gyrfalcon behaved like a highly specialised ptarmigan (<i>Lagopus spp.</i>) predator. Gyrfalcon’s functional response to ptarmigan was close to density independent, and ptarmigan remained the dominating prey even in areas with the lowest ptarmigan density. The gyrfalcon did not respond functionally to microtine rodents (i.e. lemmings and voles) and it was clear that the gyrfalcon did not use microtines as an alternative prey category to ptarmigan. As the gyrfalcons did not switch to any alternative prey when ptarmigan was scarce, their reproductive success seemed to be directly dependent on the amount of ptarmigan available in the breeding territories. Of the two ptarmigan species in the study area, rock ptarmigan (<i>L. mutus</i>) dominated gyrfalcon’s diet. Locally, the proportion of rock ptarmigan in gyrfalcons’ diets showed a positive relationship to the expected availability of rock ptarmigan in the breeding territories, indicating a density dependent utilisation. </p><p>The rough-legged buzzard behaved like a highly specialised microtine rodent predator and Norwegian lemming (<i>Lemmus lemmus</i>) was its preferred microtine species. The buzzards showed a type 2 functional response to lemmings. Surprisingly though, they also had a type 3 functional response to grey-sided voles (<i>Clethrionomus rufocanus</i>). We present an optimal diet model where a central place forager, during good food conditions, benefits from partial prey preference, which renders separate functional responses to each prey category. We discuss how the double functional responses of the buzzard affect the population dynamics of sympatric vole species, on both temporal and spatial scales.</p><p>The golden eagle behaved like a generalist predator, and it preyed on all major prey categories in the study area: microtines, ptarmigan, mountain hare, (<i>Lepus timidus</i>) and reindeer (<i>Rangifer tarandus</i>). It seemed to respond functionally to microtine rodent fluctuations with an increased consumption of lemmings during a peak year in the microtine rodent cycle. The golden eagle showed a numerical response to its main prey, the ptarmigan. </p><p>Ptarmigan, microtine rodents and hares seemed to have synchronized population fluctuations in the study area. Such synchronized population fluctuations are believed to be generated by predation. Although the three raptors are the main predators of their community, their predation patterns fail to explain the observed prey population dynamics in the study area. </p>
2

The juvenile three-spined stickleback : model organism for the study of estrogenic and androgenic endocrine disruption in laboratory and field

Hahlbeck, Edda January 2004 (has links)
<p>Industrial and domestic sewage effluents have been found to cause reproductive disorders in wild fish, often as a result of the interference of compounds in the effluents with the endocrine system. This thesis describes laboratory-based exposure experiments and a field survey that were conducted with juveniles of the three-spined stickleback, <i>Gasterosteus aculeatus</i>. This small teleost is a common fish in Swedish coastal waters and was chosen as an alternative to non-native test species commonly used in endocrine disruption studies, which allows the comparison of field data with results from laboratory experiments.</p><p>The aim of this thesis was to elucidate 1) if genetic sex determination and differentiation can be disturbed by natural and synthetic steroid hormones and 2) whether this provides an endpoint for the detection of endocrine disruption, 3) to evaluate the applicability of specific estrogen- and androgen-inducible marker proteins in juvenile three-spined sticklebacks, 4) to investigate whether estrogenic and/or androgenic endocrine disrupting activity can be detected in effluents from Swedish pulp mills and domestic sewage treatment plants and 5) whether such activity can be detected in coastal waters receiving these effluents.</p><p>Laboratory exposure experiments found juvenile three-spined sticklebacks to be sensitive to water-borne estrogenic and androgenic steroid substances. Intersex – the co-occurrence of ovarian and testicular tissue in gonads – was induced by 17β-estradiol (E2), 17α-ethinylestradiol (EE2), 17α-methyltestosterone (MT) and 5α-dihydrotestosterone (DHT). The first two weeks after hatching was the phase of highest sensitivity. MT was ambivalent by simultaneously eliciting masculinizing and feminizing effects. When applying a DNA-based method for genetic sex identification, it was found that application of MT only during the first two weeks after hatching caused total and apparently irreversible development of testis in genetic females. E2 caused gonad type reversal from male to female. E2 and EE2 induced vitellogenin - the estrogen-responsive yolk precursor protein, while DHT and MT induced spiggin – the androgen-responsive glue protein of the stickleback.</p><p>None of the effluents from two pulp mills and two domestic sewage treatment plants had any estrogenic or androgenic activity. Juvenile three-spined sticklebacks were collected during four subsequent summers at the Swedish Baltic Sea coast in recipients of effluents from pulp mills and a domestic sewage treatment plant as well as remote reference sites. No sings of endocrine disruption were observed at any site, when studying gonad development or marker proteins, except for a deviation of sex ratios at a reference site.</p><p>The three-spined stickleback – with focus on the juvenile stage – was found to be a sensitive species suitable for the study of estrogenic and androgenic endocrine disruption.</p>
3

Protein Expression in Baltic Sea Blue Mussels Exposed to Natural and Anthropogenic Stress : The use of stress inducible proteins in ecotoxicological studies

Olsson, Björne January 2005 (has links)
<p>The focus of this thesis is the early detection of stress in the environment. It has been proposed that studies on the cellular level would detect stress reactions earlier in time compared to common physiological methods. In a series of experiments we investigated how different stress factors, both natural and introduced by man, affect levels of stress proteins. One- and two-dimensional gels were used to determine individual proteins and families of proteins. The two-dimensional gels were also used in a proteomic approach, were the presence and absence of proteins after treatment was observed, and the protein expression signatures (PES) were identified. </p><p>Baltic <i>Mytilus edulis</i> was used in all experiments and it is evident that earlier observed differences in physiological rates and pollution sensitivity, compared to marine mussels, is also manifested as lower concentrations of stress proteins after exposure to copper and cadmium. When the Baltic mussels were allowed to acclimate for one month the difference decreased, suggesting an environmentally induced difference (paper I). Pre-exposure to heat before exposure to either a second heat-shock or cadmium was found to enhance the levels of HSP70 and thus tolerance, significantly (paper II). Exposure to a mixture of stress factors (PCB, copper and lowered salinity) revealed synergistic, additive and antagonistic effects in induction of 6 different stress proteins. When analyzing a large number of proteins it was shown that it is possible to identify PES with this technique, and we hypothesize that it could be possible to separate responses to mixtures of stress factors (Papers III and IV). Different techniques were also applied to analyze the protein expression pattern when mussels were exposed to PAH- and PCB-fractions extracted from Baltic Sea sediments. In this experiment the protein assays were accompanied by physiological measurements. All methods indicated stressed conditions, but the variation between individual mussels within treatments was smaller in terms of protein response than for physiological parameters (paper V). It is concluded that measuring the induction of stress proteins is a reliable way to detect stressful conditions. Proteins visualized on a one dimensional gel give a “gross” picture of an organism’s condition. The major challenge is to identify the origin and severity of the elucidated stress response. Further mapping of two-dimensional gels suggested that protein patterns are specific to type and level of stress. </p><p>A most important future step is to establish links between sub-cellular protein response to well known physiological effects. This should include long term experiments where altered protein expression signatures are linked to life history characteristics like survival, growth and reproductive success.</p>
4

The evolution of mating rates in <i>Pieris napi</i>

Bergström, Jonas January 2004 (has links)
<p>In the green-veined white butterfly (<i>Pieris napi</i>), females obtain direct fitness benefits from mating multiply and studies have shown that fitness increases seemingly monotonically with number of matings. The reason is that at mating males transfer a large nutritious gift (a so called nuptial gift) to the females that the females use to increase both their fecundity and lifespan. In addition, if exposed to poor food conditions as larvae, females mature at a smaller size compared to males. Accordingly, it was suggested that smaller females could compensate for their size through nuptial feeding by, for instance, mating more frequently. We did not find any support for that hypothesis. On the contrary, larger females remated sooner and had a higher lifetime number of matings. Neither were smaller females able to compensate in any other way, because singly mated females and multiply mated females suffered to the same extent from their smaller size. This thesis also shows that despite the positive relationship between fitness and number of matings, there is a large variation in female mating frequency in wild populations and about every second female mates only once or twice. This variation is not dependent on how often females get courted by males, because female mating frequency was shown not to be affected by male courtship intensity. Hence, the reason for the low mating frequency could either be that males have evolved the ability to manipulate females to mate at a suboptimal rate as a measure of protection against sperm competition, or alternatively, that female mating rate is suppressed by some costs. Using two selection lines, artificially selected for either a high or a low mating rate, we showed that the variation in mating rate was mainly a female trait because which line the females were from affected their mating rate whereas which line the male was from did not. This implies that females mate at a low rate due to hidden costs or due to constraints. The same study also showed that females with a high "intrinsic" mating rate lived shorter, but only when denied remating. This led us to test the hypothesis that the cost females face is to have the ability to mate at a high rate but the cost is only paid when remating opportunities are scarce. However, we found no support for such an idea, because females with a high intrinsic mating rate held in a cold environment where the butterflies were prevented from flying and feeding did not live shorter. Neither was there an effect of a female’s mating rate on her ability to quickly break down and convert male nutrient gifts into egg material. Female mating rate did, on the other hand, affect dispersal tendency, with low mating rate females being more inclined to fly between different habitats. The underlying reason for this is still to be explored.</p>
5

Spatial heterogeneity and biotic interactions : scaling from experiments to natural systems

Bergström, Ulf January 2004 (has links)
<p>Much of current ecological theory stems from experimental studies. These studies have often been conducted in closed systems, at spatial scales that are much smaller than the systems of interest. It is known that the outcome of these experiments may be seriously affected by artefacts associated with the caging procedures, as well as by the actual difference in spatial scale between experimental and target system. Yet, quantitative methods for estimating and removing artefacts of enclosure and for extrapolating experimental results to the scales of natural systems are largely lacking.</p><p>The aim of this thesis was to confront some of the problems encountered when scaling from experiments to nature in studies on predator-prey systems, with focus on effects of changes in spatial heterogeneity. Specifically, I examined mechanisms that may cause consumption rate estimates to depend on the size of the experimental arena. I also studied methods for scaling up these process rate estimates to natural predator-prey systems. The studies were performed on invertebrate predator-prey systems found in the northern Baltic Sea. Initially, a descriptive study of small-scale distribution patterns was performed, in order to get background information on how the behaviour of the organisms was manifested in the spatial structure of the community. Experimental studies of two predator-prey systems exposed an artefact that may be widespread in experiments aiming at quantifying biotic interactions. It is caused by predator and prey aggregating along the walls of the experimental containers. This behaviour affects the encounter rate between predator and prey, thereby causing consumption rates to be scale-dependent. Opposing the common belief that larger arenas always produce less biased results, this scale effect may instead be reduced by decreasing arena size. An alternative method for estimating the magnitude of, and subsequently removing, the artefact caused by aggregation along the arena wall was presented.</p><p>Once unbiased estimates of process functions have been derived, the next step is to scale up the functions to natural systems. This extrapolation entails a considerable increase in spatial heterogeneity, which may have important implications for the dynamics of the system. Moment approximation provides a method of taking the heterogeneity of natural populations into account in the extrapolation process. In the last study of the thesis, the concepts of moment approximation and how to estimate relevant heterogeneity were explained, and it was shown how the method may be used for adding space as a component to a dynamic predator-prey model. It was concluded that moment approximation provides a simple and useful technique for dealing with effects of spatial variation, and that a major benefit of the method is that it provides a way of visualising how heterogeneity affects ecological processes.</p>
6

Vegetation patterns and processes in riparian landscapes

Malm Renöfält, Birgitta January 2004 (has links)
<p>The objective of this study was to increase understanding of the processes structuring and controlling the species richness of riparian plant communities. In particular, I examined the unimodal relationship, found in many rivers, between plant species richness and location along the river corridor. The most important finding was that this pattern is dynamic and varies with time, most likely in response to large-scale flood disturbances. I also found that the sensitivity to flood disturbance varied with the environmental setting of the riparian reaches. Turbulent sections of the river retained high species richness, whereas tranquil reaches had significantly lower species richness in years following high and prolonged flooding, compared to a period without extreme flood events. Riparian soils along turbulent reaches are more resistant to oxygen depletion during floods, a factor which is likely to contribute to the maintenance of species richness. </p><p>The finding that the species richness pattern varied with time led me to ask which factors control plant diversity along riparian zones. I addressed this question by formulating three contrasting, although not mutually exclusive, hypotheses: (1) longitudinal patterns in riparian plant species richness are governed by local, river-related processes independent of the regional species richness, (2) riparian plant species richness is controlled by dispersal along the river, i.e., longitudinal control, and (3) the variation in riparian plant species richness mirrors variation in regional richness, i.e., lateral control. I found indications of all three types of control, although local factors seemed to fit most of the criteria. Riparian species richness was not significantly correlated to species richness in the surrounding upland valley. It was however significantly negatively correlated to soil pH, a local habitat factor of the reach. The fact that the species richness pattern varied in time, corresponding to the presence or absence of extreme flood events suggest that it is influenced by local disturbance regimes. The potential for control by longitudinal dispersal was found to be highest in the middle reaches of a river. Here, the similarity between upland and riparian vegetation was lowest, and invasibility (germination ability) was highest. Earlier work has shown that regulated rivers have an inverted species richness pattern compared to free-flowing rivers, with lowest species richness in the middle reaches. One potential mechanism behind this could be varying susceptibility to disturbance along the river. I tested this by experimentally disturbing the vegetation, applying the same level of disturbance along an entire free-flowing river. However, the response to experimental disturbance did not vary with location, likely because of a major flood disturbance preceding the experiment.</p>
7

Factors Affecting the Distribution of Rocky-Shore Macroalgae on the Swedish Coast : Morphological, Physiological, Reproductive and Genetic Aspects

Johansson, Gustav January 2002 (has links)
<p>The aim of this thesis was to examine factors affecting the distribution of macroalgal species both vertically (depth zonation) and geographically along the Baltic Sea salinity gradient. Interactions between the physical environment and basic biological traits of the algae are emphasised.</p><p>Previously well-described macroalgal vegetation profiles were re-investigated. Long-term changes of the vegetation that can be coupled to an increased large-scale eutrophication were recorded in both the Baltic Sea and in the Skagerrak.</p><p>Photosynthetic properties of macroalgae with different morphologies from typical depth zonations in the Skagerrak and the Baltic Sea were assessed. A novel method that makes it possible to classify macroalgal species along a morphological gradient based on photosynthetic properties is presented. Such a gradient can be used as an alternative to more discrete subdivisions into functional-form groups.</p><p>Small-scale variation in the natural sediment load was shown to affect the composition of sublittoral rocky-shore macroalgal communities in a long-term field experiment. Generally, species with an extended reproductive period were more tolerant to sedimentation than species depending on short periods of spore release. The effect of the sediment treatments increased with depth.</p><p>Field experiments in the Baltic Sea showed that fragments of <i>Furcellarialumbricalis</i>, <i>Polysiphoniafucoides</i> and <i>Rhodomela confervoides</i> are able to reattach to the substrate under field conditions. This enables persistence of populations since these species are practically sterile in the area. Field observations suggested that sessile animals can facilitate the fixation of algal fragments to the substrate.</p><p>Genetic variation of the chlorophyte <i>Cladophorarupestris</i> was assessed by allozyme electrophoresis. Two genetically differentiated groups of populations were found, one Baltic Sea group and one North Sea group, with a distinct border in the southern Kattegat near the entrance to the Baltic Sea.</p>
8

Female Reproductive Strategies in the Ruff (<i>Philomachus pugnax</i>)

Thuman, Katherine January 2003 (has links)
<p>Traditionally, females have been considered to be strictly monogamous. Today, we know that females in the majority of species actively seek out and mate with several males. Trying to understand female preferences, including what benefits mate choice entails, has been the focus of intense research during the last decades. Females can gain both direct (e.g. access to better territories or paternal care) and indirect (i.e. genetic) benefits. The aim of this thesis is to further our understanding of the female reproductive strategies in the ruff, <i>Philomachus pugnax</i> (Aves, Scolopacidae). The ruff is a lekking wader, where males gather on leks to display to females that come there to mate. Males do not provide any paternal care to the offspring. Lekking systems are ideal for studying indirect benefits of female choice, as females do not gain any direct benefits from males.</p><p>Females mated with several males and 50% of the broods were fathered by at least two males. The level of genetic similarity between two parents has previously been shown to be an important source of variation in offspring fitness. Males that were less closely related to the female fathered more offspring in broods with multiple paternity, such that females that mated multiply gained in terms of receiving more outbred offspring. There did not, however, appear to be an overall female preference for less closely related males. There are two genetically determined male reproductive strategies in the ruff, that differ in behaviour and morphology. There was no evidence for females taking male strategy into account when choosing a partner.</p><p>Female post-fertilisation strategies may also influence fitness, e.g. through differential investment in eggs, gender of the offspring and choice of breeding habitat. Females allocated sex in a non-random manner dependent upon body condition, such that females in good condition had more daughters.</p><p>Females were found to nest in higher than average vegetation and in areas with higher than average abundance of insects, factors likely to influence predation rates on both eggs and young, as well as foraging opportunities for the precocial young. Further, females were faithful to their previous breeding site and usually nested within meters of their previous nest. Hatching success did not, however, affect a female’s decision to return or not.</p>
9

Structural Growth in Mountain Birch, <i>Betula pubescens</i> ssp. <i>czerepanovii</i>

Borg, Christina January 2005 (has links)
<p>In this thesis, I have studied long shoot performance in the monoecious, deciduous tree <i>Betula</i> <i>pubescens</i> ssp. <i>czerepanovii</i>. In field studies and a common garden experiment, I have a) studied how environmental variations affect the performance of long shoots in mountain birch, and b) described the relationship between long shoot performance and characteristics of the parent long shoot.</p><p>I have shown that difference in long shoot performance to some extent can be explained by environmental variables such as temperature, precipitation and global radiation the current and previous summer, annual soil and air temperatures, and the length of growing season. For example, a low summer temperature the previous summer had a negative effect on a majority of long shoot characteristics. Variation in shoot characteristics was of the same magnitude along the regional east-western gradient as along the local altitudinal gradient. Variation among individual trees was of the same magnitude as variation among years. Further, long shoot performance was affected by the parent shoot characteristics and reflects that primordia of different organs are formed in the previous summer. </p><p>On several occasions, freezing damage to mountain birch has been observed on Mt Njulla in northernmost Sweden. Following such damage, fewer but larger leaves emerge. Damages were compensated for with increased number of buds on long shoots produced the same year and one year after damage. Moreover, there were more new long shoots born on short shoots among damaged trees. Dormant buds and short shoots fulfil important functions in a fluctuating environment and as an adaptation to recurring damages of different origin and severity.</p><p>Differences in the performance among mountain birch saplings grown in a common-garden at Abisko could to a large degree be explained by their origin. Further, saplings from Sweden and from Iceland responded differently to defoliation, and fertilization did not alter the responses to defoliation.</p>
10

Vegetation patterns and processes in riparian landscapes

Malm Renöfält, Birgitta January 2004 (has links)
The objective of this study was to increase understanding of the processes structuring and controlling the species richness of riparian plant communities. In particular, I examined the unimodal relationship, found in many rivers, between plant species richness and location along the river corridor. The most important finding was that this pattern is dynamic and varies with time, most likely in response to large-scale flood disturbances. I also found that the sensitivity to flood disturbance varied with the environmental setting of the riparian reaches. Turbulent sections of the river retained high species richness, whereas tranquil reaches had significantly lower species richness in years following high and prolonged flooding, compared to a period without extreme flood events. Riparian soils along turbulent reaches are more resistant to oxygen depletion during floods, a factor which is likely to contribute to the maintenance of species richness. The finding that the species richness pattern varied with time led me to ask which factors control plant diversity along riparian zones. I addressed this question by formulating three contrasting, although not mutually exclusive, hypotheses: (1) longitudinal patterns in riparian plant species richness are governed by local, river-related processes independent of the regional species richness, (2) riparian plant species richness is controlled by dispersal along the river, i.e., longitudinal control, and (3) the variation in riparian plant species richness mirrors variation in regional richness, i.e., lateral control. I found indications of all three types of control, although local factors seemed to fit most of the criteria. Riparian species richness was not significantly correlated to species richness in the surrounding upland valley. It was however significantly negatively correlated to soil pH, a local habitat factor of the reach. The fact that the species richness pattern varied in time, corresponding to the presence or absence of extreme flood events suggest that it is influenced by local disturbance regimes. The potential for control by longitudinal dispersal was found to be highest in the middle reaches of a river. Here, the similarity between upland and riparian vegetation was lowest, and invasibility (germination ability) was highest. Earlier work has shown that regulated rivers have an inverted species richness pattern compared to free-flowing rivers, with lowest species richness in the middle reaches. One potential mechanism behind this could be varying susceptibility to disturbance along the river. I tested this by experimentally disturbing the vegetation, applying the same level of disturbance along an entire free-flowing river. However, the response to experimental disturbance did not vary with location, likely because of a major flood disturbance preceding the experiment.

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