• Refine Query
  • Source
  • Publication year
  • to
  • Language
  • 76
  • 16
  • 15
  • 9
  • 4
  • 3
  • 2
  • 2
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • Tagged with
  • 156
  • 156
  • 25
  • 23
  • 16
  • 15
  • 15
  • 15
  • 13
  • 12
  • 11
  • 11
  • 11
  • 10
  • 10
  • 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.
61

Predicting Vulnerability of Fishes

O'Malley, Stacey Lee 27 July 2010 (has links)
Conservation biology would benefit from methods that identify species at risk in a proactive manner, rather than through post-hoc conservation assessments. This study examines the utility of four potential indices for predicting vulnerability in fishes: total body length; trophic level; intrinsic vulnerability score; and, resilience. Statistical analysis was done to determine if correlations existed between any of these four indices and known levels of risk in marine and freshwater Canadian fishes. Results show the success of two of these indices to predict risk: fished species over 78.33 centimeters total length, or with intrinsic vulnerability scores over 57.41 are more highly vulnerable to becoming at risk. Over 20% of Canadian fished species of unknown conservation status are therefore currently vulnerable, and possibly at risk of extinction. This study shows vulnerability indices allow a rapid prioritization of fishes at risk of extinction, and can thus help achieve proactive conservation even in the absence of population decline data.
62

Predicting Vulnerability of Fishes

O'Malley, Stacey Lee 27 July 2010 (has links)
Conservation biology would benefit from methods that identify species at risk in a proactive manner, rather than through post-hoc conservation assessments. This study examines the utility of four potential indices for predicting vulnerability in fishes: total body length; trophic level; intrinsic vulnerability score; and, resilience. Statistical analysis was done to determine if correlations existed between any of these four indices and known levels of risk in marine and freshwater Canadian fishes. Results show the success of two of these indices to predict risk: fished species over 78.33 centimeters total length, or with intrinsic vulnerability scores over 57.41 are more highly vulnerable to becoming at risk. Over 20% of Canadian fished species of unknown conservation status are therefore currently vulnerable, and possibly at risk of extinction. This study shows vulnerability indices allow a rapid prioritization of fishes at risk of extinction, and can thus help achieve proactive conservation even in the absence of population decline data.
63

The Role of Threshold Size in Insect Metamorphosis and Body Size Regulation

Preuss, Kevin Michael January 2010 (has links)
<p>The initiation of metamorphosis causes the cessation of the larval growth period which determines the final body size of adult insects. Because larval growth is roughly exponential, differences in timing the initiation of metamorphosis can cause large differences body size. Although many of the processes involved in metamorphosis have been well characterized, little is known about how the timing of the initiation of metamorphosis is determined. </p> <p>Using different strains from <italic>Tribolium castaneum<italic>, <italic>Tribolium freemani<italic>, and <italic>Manduca sexta<italic> and varied nutritional conditions, I was able to document the existence of a threshold size, which determines when the larva becomes competent to metamorphose. Threshold size, however, does not dictate the exact timing of initiation. The exact timing for the initiation of metamorphosis is determined by a pulse of the molting hormone, ecdysone, but only after threshold size has been reached. Ecdysone pulses before the larva attains threshold size only cause the larva to molt to another larval instar. These results indicate the timing of metamorphosis initiation is controlled by two factors: (1) attainment of threshold size, at which the larva becomes competent to initiate metamorphosis and (2) the timing of an ecdysone pulse after attaining threshold size. </p> <p>I hypothesize the attainment of threshold size, and therefore competence to metamorphose, is mediated by the effect of changing juvenile hormone concentrations caused by the increase in size of the larva. While the larval body grows nearly exponentially, the corpora allata, which secretes juvenile hormone, grows very little if at all. The difference in relative growth causes juvenile hormone concentrations to gradually become diluted. When juvenile hormone concentrations fall below a threshold, changes in protein-protein binding occur that can cause changes in signaling networks and ultimately gene expression. These changes make the larva competent for metamorphosis. </p> <p>I have demonstrated that only threshold size is consistently correlated with body size; other growth parameters such as growth rate, duration of instars, or number of instars do not consistently correlate with variation in body size. Using the black mutant strain of <italic>M. sexta<italic> I have shown that lower juvenile hormone titers correlate with lower threshold sizes. My hypothesis is consistent with the large body of literature indicating the involvement of juvenile hormone. I also hypothesize that the diversity of metamorphosis types in holometabolous insects can be explained by heterochronic shifts in the timing of threshold size and other developmental events related to metamorphosis. The heterochronic shifts affect not only the morphology of organs, but can also affect the overall phenotypic response of the larva to changes in the environment. The different phenotypic responses among species may make the more or less suited for certain types of niches.</p> / Dissertation
64

Parameterizing Image Quality of TOF versus Non-TOF PET as a Function of Body Size

Wilson, Joshua Mark January 2011 (has links)
<p>Positron emission tomography (PET) is a nuclear medicine diagnostic imaging exam of metabolic processes in the body. Radiotracers, which consist of positron emitting radioisotopes and a molecular probe, are introduced into the body, emitted radiation is detected, and tomographic images are reconstructed. The primary clinical PET application is in oncology using a glucose analogue radiotracer, which is avidly taken up by some cancers.</p><p>It is well known that PET performance and image quality degrade as body size increases, and epidemiological studies over the past two decades show that the adult US population's body size has increased dramatically and continues to increase. Larger patients have more attenuating material that increases the number of emitted photons that are scattered or absorbed within the body. Thus, for a fixed amount of injected radioactivity and acquisition duration, the number of measured true coincidence events will decrease, and the background fractions will increase. Another size-related factor, independent of attenuation, is the volume throughout which the measured coincidence counts are distributed: for a fixed acquisition duration, as the body size increases, the counts are distributed over a larger area. This is true for both a fixed amount of radioactivity, where the concentration decreases as size increases, and a fixed concentration, where the amount radioactivity increases with size.</p><p>Time-of-flight (TOF) PET is a recently commercialized technology that allows the localization, with a certain degree of error, of a positron annihilation using timing differences in the detection of coincidence photons. Both heuristic and analytical evaluations predict that TOF PET will have improved performance and image quality compared to non-TOF PET, and this improvement increases as body size increases. The goal of this dissertation is to parameterize the image quality improvement of TOF PET compared to non-TOF PET as a function of body size. Currently, no standard for comparison exists.</p><p>Previous evaluations of TOF PET's improvement have been made with either computer-simulated data or acquired data using a few discrete phantom sizes. A phantom that represents a range of attenuating dimensions, that can have a varying radioactivity distribution, and that can have radioactive inserts positioned throughout its volume would facilitate characterizing PET system performance and image quality as a function of body size. A fillable, tapered phantom, was designed, simulated, and constructed. The phantom has an oval cross-section ranging from 38.5 &times; 49.5 cm to 6.8 &times; 17.8 cm, a length of 51.1 cm, a mass of 6 kg (empty), a mass of 42 kg (water filled), and 1.25-cm acrylic walls.</p><p>For this dissertation research, PET image quality was measured using multiple, small spheres with diameters near the spatial resolution of clinical whole-body PET systems. Measurements made on a small sphere, which typically include a small number of image voxels, are susceptible to fluctuations over the few voxels, so using multiple spheres improves the statistical power of the measurements that, in turn, reduces the influence of these fluctuations. These spheres were arranged in an array and mounted throughout the tapered phantom's volume to objectively measure image quality as a function of body size. Image quality is measured by placing regions of interest on images and calculating contrast recovery, background variability, and signal to noise ratio.</p><p>Image quality as a function of body size was parameterized for TOF compared to non-TOF PET using 46 1.0-cm spheres positioned in six different body sizes in a fillable, tapered phantom. When the TOF and non-TOF PET images were reconstructed for matched contrast, the square of the ratio of the images' signal-to-noise ratios for TOF to non-TOF PET was plotted as a function, <italic>f</italic>(<italic>D</italic>), of the radioactivity distribution size, <italic>D</italic>, in cm. A linear regression was fit to the data: <italic>f</italic>(<italic>D</italic>) = 0.108<italic>D</italic> - 1.36. This was compared to the ratio of <italic>D</italic> and the localization error, <italic>&sigma;<sub>d</sub></italic>, based on the system timing resolution, which is approximately 650 ps for the TOF PET system used for this research. With the image quality metrics used in this work, the ratio of TOF to non-TOF PET fits well to a linear relationship and is parallel to <italic>D/&sigma;<sub>d</sub></italic>. For <italic>D</italic> < 20 cm, there is no image quality improvement, but for radioactivity distributions <italic>D</italic> > 20 cm, TOF PET improves image quality over non-TOF PET. PET imaging's clinical use has increased over the past decade, and TOF PET's image quality improvement for large patients makes TOF an important new technology because the occurrence of obesity in the US adult population continues to increase.</p> / Dissertation
65

Is Slim Model Effective? Influences of Model¡¦s Body Size, Race and Product Type in Advertising

Leong, Si-kei 30 August 2011 (has links)
In daily life, information of losing weight or improving fitness can be seen everywhere. For example, being skinny is pretty and healthy. No matter in Western or Asian countries, we can observe that standardized ideal image has been established for years through models in advertising. Also, physical attractiveness pursuit becomes important in the global society because of advertising. Hence, more and more researchers interested in body image will take appearance and body shape into account. However, most of previous research focuses on the negative effect of self-consciousness induced by images of being thin. By distinguishing model¡¦s body size into slim and large size, this research examines the factors that may influence the effects of model¡¦s body size in advertising. The present study uses experimental design to investigate the advertising effects of model¡¦s body size (slim vs. large), model¡¦s race (Asia vs. Western), and product type (utilitarian vs. hedonic). Thus, a 2¡Ñ2¡Ñ2 factorial design is conducted. The ad effects are measured by product evaluation and attitude toward the model to observe the response under eight different and fictitious scenarios. The results indicate that, a model with slim-size is more effective that with large-size. Such influences are stronger when an Asian model is used. Howerever, no matter slim or large the model¡¦s size is, the effect of advertising on utilitarian product and hedonic product are identical when using a Western model. In addition, female participants generally give lower credit on advertising evaluation than male ones, reflecting obviously in their preference of model. According to these findings, this study suggests that marketers should consider not only the product they promote but also the congruency of race between ad model and target consumers, as well as attractive slim-size models, in order to enhance the advertising effects.
66

Geographic variation of Niviventer coxingi in body size and mitochondrial D-loop region

Chan, Hsiao-ting 13 February 2004 (has links)
Summarized the results of previous studies, the body size of Niviventer coxingi seemed to be correlated with altitude. For more exact evidence, geographic variations of body lengths and appendage sizes among areas were examined. Moreover, Freckleton et al. (2003) indicated that phylogenetic relationships may affect the results of one¡¦s study while variation of body size is discussed. Therefore, the phylogeographic variation among different areas was also examined in this study. The body lengths of N. coxingi in higher altitude (Fong-gang, 1700 m) were shorter than in lower altitude (Shan-ping 700 m). Body lengths of N. coxingi in Shan-ping were longer than other areas but Wu-shih-kang; and N. coxingi in Fong-gang were longer than those in Wu-tou Mountain; but no significant differences were found among other areas. No significant differences were found in appendage sizes but hind-foot length. Significant differences of the hind-foot length were only found between Shan-ping which had the longest hind-foot lengths in average and those in Wu-tou Mountain which had the shortest. No correlations were found between altitudes and the body length or appendage sizes of N. coxingi. The phylogenetic relationships based on D-loop region of N. coxingi were reconstructed by neighbor-joining, maximum parsimony and maximum-likelihood methods. An N. culturatus was used to be an outgroup. All three trees represented similar patterns. Although some individuals from neighborhood grouped together, some individuals from the same area represented distantly. Moreover, many branches represented in the root of the consensus trees because of the low bootstrap value. The results revealed the geographic variations did not correlated with their phylogenetic relationships and the heat conservation/ dissipation mechanism, which was the traditional explanation of Bergmann¡¦s rule, was not appropriate for N. coxingi, either.
67

Ecological Factors and Historical Biogeography Influence the Evolutionary Divergence of Insular Rodents

Durst, Paul Alexander Pinette January 2014 (has links)
<p>Islands have been the inspiration for some of evolutionary biology's most important advances. This is largely due to the unique properties of islands that promote the differentiation of island species from their mainland counterparts. Rodents are widely distributed across even the most remote islands, a rarity among mammals, making them uniquely suited to study the factors leading to the divergence of insular species. In this dissertation, I use two case studies to examine the morphological and genetic divergences that take place in an insular environment.</p><p>In chapters one and two, I examine how different factors influence insular body size change in rodents. In chapter one, I examine factors influencing the direction of island body size change using classification tree and random forest (CART) analyses. I observe strong consistency in the direction of size change within islands and within species, but little consistency at broader taxonomic scales. Including island and species traits in the CART analyses, I find mainland body mass to be the most important factor influencing size change. Other variables are significant, though their roles seem to be context-dependent.</p><p>In chapter two, I use the distributions of mainland rodent population body sizes to identify `extreme' insular rodent populations and compare traits associated with those populations and their islands with those island populations of a more typical size. I find that althought there is no trend among all insular rodents towards a larger or smaller size, `extreme' populations are more likely to increase in size. Using CART methods, I develop a predictive model for insular size change that identifies resource limitations as the main driver when insular rodent populations become `extremely small'. </p><p>Chapters three and four shift their focus to a single rodent species, the deer mouse <italic>Peromyscus maniculatus</italic>, as they examine the genetic differentiation of deer mice across the California Channel Islands and the nearby mainland. In chapter three, I sequence a region of the mitochondrial control region for individuals from 8 populations across the northern Channel Islands and two mainland sites, and I analyze these sequences by calculating population genetics parameters and creating a Bayesian inference tree and a statistical parsimony haplotype network. All of these analyses reveal significant divergences between island and mainland populations. Among the islands, Santa Barbara and Anacapa islands both display unique genetic signatures, but the other northern islands remain relatively undifferentiated.</p><p>In chapter four, I genotype individuals from the previous chapter at 5 microsatellite loci, I calculate additional population genetics parameters and I utilize a Bayesian clustering algorithm to examine the similarities and differences between nuclear and mitochondrial analyses. I find the nuclear data to be largely congruent with the mitochondrial analyses; there are significant differences between island and mainland populations, and Anacapa Island is significantly differentiated from the other islands. Unlike the previous analyses, Santa Barbara Island is not significantly different from the northern islands, yet San Miguel Island has a unique genetic signature. </p><p>These studies underscore the importance of ecological processes and historical biogeography in the generation of diversity, and they highlight the role of islands as drivers of evolutionary divergence.</p> / Dissertation
68

Life histories and energetics of bumble bee (Bombus impatiens) colonies and workers

Cao, Nhi January 2014 (has links)
Social insect colonies are complex systems with emergent properties that arise from the cooperation and interaction amongst individuals within colonies. By dividing reproduction and physical labor amongst them, individuals contribute to the growth and ecological success of their colonies, a success that is greater than individuals could achieve on their own. A key characteristic of social insects is a division of labor amongst workers that is determined primarily either by age, morphology, or dominance. Social insects are considered one of the most ecologically successful groups of organisms on earth. Colony life cycles include: 1) growth, in which workers are produced, 2) reproduction, in which queens and males with reproductive capabilities are produced, and 3) senescence. In life history theory, phenotypic plasticity (i.e. a change in phenotype in response to an environmental change), allows organisms to adjust and optimize fitness in response the change in environments. Central to life history theory is the idea that traits have costs and benefits. Using an energetics framework that considers the costs and benefits of traits contributes to our understanding as to why organisms exhibit the sets of traits that they have within their ecological environments. Using the annual bumble bee Bombus impatiens, my dissertation investigates the effects of resource availability on worker production and on the relative allocation of energy towards growth and reproduction within colonies. Bumble bees have a morphological division of labor and concomitantly, they show large intra-colony size variation amongst workers. Because body size is an important life history trait, I also examined the costs and benefits of producing various sized workers. Lastly, I examined the association among worker body size, metabolic rate (a measure of maintenance costs), and lifespan.
69

Genome Size Diversity and Patterns within the Annelida

Forde, Alison Christine 24 January 2013 (has links)
This thesis concerns genomic variation within the Annelida, for which genome size studies are few and provide data for only a handful of groups. Genome size estimates were generated using Feulgen image analysis densitometry for 35 species of leeches and 61 polychaete species. Relationships were explored utilizing collection location and supplementary biological data from external sources. A novel, inverse correlation between genome size and maximum adult body size was found across all leeches. Leeches that provide parental care had significantly larger genome sizes than leeches that do not. Additionally, specimens identified as Nephelopsis obscura exhibited geographic genome size variation. Within the Polychaeta, Polar region polychaete genomes were significantly larger than those of Atlantic and Pacific polychaetes. These studies represent the first exploration of leech genome sizes, and provide base evidence for numerous future studies to examine relationships between genome size and life history traits across and within different annelid groups.
70

The role of body mass index and body shape in perceptions of body attractiveness cross-cultural study /

Aghekyan, Marine Connell, Lenda Jo. Ulrich, Pamela V. January 2005 (has links) (PDF)
Thesis(M.S.)--Auburn University, 2005. / Abstract. Vita. Includes bibliographic references.

Page generated in 0.0559 seconds