This research serves two main purposes: to create an analyzed edition of Ray Brown's bass lines from the Oscar Peterson Trio's 1964 recording We Get Requests, and to better understand Brown's lines through the lens of Ray Brown's Bass Method. This comparative analysis identifies significant events in the recorded music that closely relate to or resemble exercises from the book. By analyzing the music from the lens of Ray Brown's Bass Method, performers, students, and educators will gain a stronger understanding of the application of select technical devices provided by Brown in his book. The most prominent techniques discussed include scales and intervals, major triads, minor triads, and chords, exercises in tenths, rhythm patterns with drops, and diminished patterns. These evidence-based conclusions have significant applications in jazz bass pedagogy by revealing potential relationships between technical ideals and practical use. Although these conclusions may seem of concern only to jazz bassists, it should in fact concern anyone who cares about the connection between pedagogy and performance.

This study examined the relationship between microhabitat use and growth of age-0 smallmouth bass in the North Anna River. The study objectives were to describe microhabitat use during summer, assess the profitability of microhabitats, and determine if and how microhabitat use could determine which individuals gained a growth advantage. Age-0 smallmouth bass changed their microhabitat use as they passed through stages of ontogenetic development and became familiar with their environment. More than 30% of the area available to brood larvae contained mean water column velocities greater than 4 cm/s and no cover. More than 80% of larvae observed after dispersing from the nest site occupied areas approximately one m deep with velocities near 0 cm/s, or large cover objects that created low velocity shelters throughout the water column. By six weeks after dispersal (when all juveniles were > 40 mm), more than 50% of juveniles occupied depths less than 60 cm and focal point velocities > 3 cm/s, and microhabitat use by large and small juveniles did not differ. In these shallow microhabitats with moderate to fast current velocities, juveniles foraged at a higher rate (5.1 bites/min on average) than in deeper and slower velocity areas (1.3 bites/min). When these foraging rates were translated into estimates of energetic profit, juveniles in the shallow-fast microhabitats gained approximately 5 j/min more than juveniles foraging in other microhabitats. Microhabitat use was the only aspect of behavior that affected the foraging rate or energetic profit gained by juvenile smallmouth bass. I examined daily rings on otoliths to track the growth of individual smallmouth bass through time. Temperature affected growth rates below 22-23°C, so that individuals spawned later grew in warmer thermal regimes and grew relatively fast during early life stages. However, individuals that spawned early and grew slowly in cooler temperatures did not suffer higher mortality and compensated for their slow growth by accumulating growth over a longer period of time. Above 22-23°C, relative growth rates were not consistent through time; a fast growing individual during one life stage could grow relatively slow during the next. If growth above the temperature threshold depended on foraging success and foraging success depended on microhabitat use, then few individuals were consistently occupying the most profitable microhabitats. In experiments in an artificial stream, juvenile smallmouth bass assessed the potential profitability of an area by the foraging rate they achieved there. They usually did not remain in an area unless they foraged well at the time they searched it, and did not appear to associate habitat characteristics with profitability. In the river, most of the microhabitats available were relatively unprofitable, so an individual that abandoned a profitable area might (depending on its foraging behavior) spend Significant time in unprofitable microhabitats and consequently reduce its growth rate. Increasing the availability or density of food resources may improve growth of juvenile smallmouth bass in the North Anna River by increasing the rate at which juveniles encounter profitable microhabitats and elevating their intake rates in profitable areas. / Ph. D.

The purpose of this study was to determine if habitat suitability criteria developed in the summer months for sma11mouth bass were transferable among streams representing different eco regions. Habitat suitability criteria were developed for depth, mean column velocity, cover and substrate for two size classes of sma1lmouth bass, 100-199mm and >200mm, in the North Anna River and Craig Creek, Virginia. Criteria that accurately describe habitat selection by a species or guild in a system different from where the criteria were developed are said to be transferable to that system. The transferability of suitability criteria between the North Anna River and Craig Creek, as well as depth and velocity criteria from Minnesota, the Huron River, Michigan and the Upper James River, Virginia, to the North Anna River and Craig Creek were tested using a 2x2 contingency table analysis. Depth criteria for the smaller sizes of sma1lmouth bass did not transfer well between regions; 4 of the 8 transferability tests (50%) failed. Depth criteria for larger sma1lmouth bass transferred to the North Anna River and Craig Creek in all cases. Velocity criteria developed for the smaller size classes did not transfer well among regions; only 3 of the 8 transferability tests were positive. Likewise, velocity criteria for larger sizes of smallmouth bass did not transfer well; only 1 of 8 tests were positive. General criteria were developed for depth and mean column velocity by averaging the suitability values reported from this and 3 other studies. General depth and velocity criteria transferred well to the North Anna River and Craig Creek for both the larger and smaller size classes of smallmouth bass; all depth tests were positive and 3 of 4 velocity tests were positive. The improved success of transferability warrants investigation of developing general criteria for smallmouth bass. Cover criteria for both size classes of smallmouth bass were transferable from the North Anna River to Craig Creek but not vice versa. Substrate heterogeneity criteria were not transferable between the North Anna River and Craig Creek for either size class of smallmouth bass. Criteria developed for the percentage of substrate particles >15cm (smallmouth bass >200mm only) were transferable from Craig Creek to the North Anna River but not vice versa. The transferability of habitat suitability criteria among regions was inconsistent and it is recommended that site-specific criteria be developed for each stream to which habitat assessments are applied. Additionally, nose velocities used were more consistent between the North Anna River and Craig Creek than were mean column velocities used. Hence, it is recommended that information on nose (focal point) velocities be incorporated into habitat studies to more accurately describe smallmouth bass velocity requirements. / Master of Science

A survey of the population characteristics of smallmouth bass (Micropterus dolomieu), rock bass (Ambloplites rupestris), and habitat conditions were conducted in the Powell River, Virginia, to identify potential habitat limitations for these species. The study area consisted of three reaches, which were determined in 1987. The upstream reach was used to monitor effects of coal mining in the upper watershed on the Powell River. The midstream reach, which was below the North Fork Powell River, was used to monitor the possible effects of this tributary and its watershed. The downstream reach appeared to have been impacted by sedimentation less than either of the other reaches. Habitat Suitability Index (HSI) models were used to identify habitat variables that were below optimum for these species in the Powell River, Virginia. Habitat sampling yielded HSI scores for smallmouth bass at each site ranging from 0.67 to 0.76, with a mean of 0.72; scores for rock bass ranged from 0.65 to 0.70, with a mean of 0.69. No trends in HSIs from upstream to downstream were evident. However, substratum, of which sand was dominant in pools, was the variable most frequently below optimum for smallmouth bass (Sl=0.21) and rock bass (SI=0.20). Values for sediment depth, embeddedness, waterborne sediment, and coal were collected in riffles, runs, and pools at 10 sites. Mean sediment depth in pools, embeddedness in riffles and runs, and waterborne sediment deposited in traps monthly in pools decreased from upstream to downstream; however, waterborne sediment in runs did not decrease. Content (by weight) of coal wastes in the substratum did not decrease from upstream to downstream. The embeddedness index in pools (= 1.0), riffles, and runs was not significantly different among the three river reaches. No differences in population abundance, biomass estimates, age and growth, or relative weights (Wr) of smallmouth bass and rock bass were found among the three river reaches. Population estimates of smallmouth bass (34.3/ha) and rock bass (116.6/ha) were lower than those in many other streams in the U.S. Catch-per-unit-effort and biomass of smallmouth bass (2.9/h, 2.6 kg/ha) and rock bass (6.6/h, 2.2 kg/ha) also were lower than those in most other streams. A total of 70 stomachs of smallmouth bass and 166 stomachs of rock bass was examined from fish collected between July 1988 and October 1989. Diets for each species, primarily crayfish and insects, showed no apparent differences among the three river reaches. Abundance of crayfish and hellgrammites were compared; greatest hellgrammite abundance was in the downstream reach (P = 0.032), and there were no significant differences in crayfish abundance among the three river reaches. HSI values showed no significant correlation with catch-per-unit-effort for smallmouth bass or rock bass. No significant correlation was found among sediment depth, catch-per-unit effort, biomass or relative weight of smallmouth bass and rock bass. No correlation was found between the embeddedness index in riffles and biomass of rock bass. There was a significant negative correlation between the embeddedness index in riffles and relative weight of smallmouth bass (P=0.016); however, no correlation existed between the embeddedness index and relative weight of rock bass. There was a significant negative correlation between the embeddedness index in riffles and growth of smallmouth bass (P=0.016); however, there was a significant positive correlation between the embeddedness index and growth of rock bass. There was a significant positive correlation between the embeddedness index in riffles and both hellgrammite abundance (P=0.031) and crayfish abundance (P=0.052) in riffles. No significant correlation was found between the amount of sediment deposited in pools and catch-per-unit-effort of smallmouth bass and rock bass. No significant correlation existed between the amount of sediment deposited in runs and biomass of rock bass. In addition, crayfish density was not correlated with relative weight of smallmouth bass or rock bass. With the available documentation that links population characteristics of smallmouth bass and rock bass to habitat, it is evident that habitat is usually the limiting factor in determining population characteristics; however, there was no significant trend in the correlations presented above. Habitat for smallmouth bass and rock bass in the Powell River, Virginia was suboptimum and sand was the dominant substratum in pools. Population estimates, catch-per-unit-effort, and biomass of smallmouth bass and rock bass in the Powell River are low compared to other U.S. streams. Although it appears that sedimentation has degraded habitat of smallmouth bass and rock bass and contributed to reduced population levels of these species in the Powell River, Virginia, my results were not statistically different among sites with measurable differences in sedimentation. / Master of Science

This thesis was partitioned into three studies. In the first study, striped bass, Morone saxatilis, (n = 16) were monitored over a 13 month period to examine the efficacy of ultrasound to determine sex and to monitor sexual maturation. Four observers reviewed all ultrasound images (n = 208) of striped bass and were able to sex male and female striped bass with 99 and 95% accuracy, respectively throughout an annual reproductive cycle. Egg diameter was highly correlated with average (r = 0.89) and maximum (r=0.92) ovarian diameter as measured by ultrasound. Spenniating males exhibited larger maximum testicular diameters (23.5 mm) than non-spermiating males (13.1 mm). Fully mature female and male striped bass exhibited maximum ovarian diameters > 30 mm and testicular diameters > 20 mm as measured by ultrasound. The results of this study indicate that ultrasound is an effective and non-invasive method that aquaculturists can use to quickly scan, sex, and assess the sexual maturation of adult male and female striped bass year-round. In the second study, photothennal manipulation was used to induce spawning out-of season and to increase the frequency of spawning in striped bass, Morone saxatilis. Forty adult striped bass, held in five environmental chambers, were exposed to compressed 6- and 9- month cycles and a 12-month reference cycle. Maximum egg diameters increased with cycle length, averaging 845 urn, 946 urn, and 1,073 um for females held on the 6-, 9-, and 12-month cycles,respectively. Females held on the 6-month cycle had smaller ovarian diameters (19.6 mm) than those held on the 9-month (27.4 mm) and 12-month (24.5 mm) cycles. Ovary diameter was highly correlated with egg diameter (r = 0.91). Spawning success (percent of females spawning) increased with cycle length, averaging 38%, 86%, and 100% in the 6-, 9-, and 12-month cycles, respectively. However, no differences in latent times, fecundity, or fertility were detected between cycles or between tank-spawned and strip-spawned females. Males held on the 6-month cycle had smaller testicular diameters (16.2 mm) than those held on 9-month (23.6 mm) and 12-month (19.2 mm) cycles. Testicular diameter of spenniating males (15.7 mm) was significantly larger than that of non-spenniating males (6.9 rnrn) in all cycles. Mortality increased with cycle length, averaging 28%, 38%, and 88% for fish held on the 6-, 9-, and 12-month cycles, respectively. Maturation and spawning were advanced by five and three months for fish held in the 6- and 9-month cycles, respectively when compared to a natural 12-month reference cycle. Fish held on the 6-month cycle matured twice within a year. However, the relatively low number of spawning females and diminished egg, ovarian, and testicular diameter of fish held on the 6-month cycle suggest that an abbreviated cycle length « 9 months) may inhibit maturation and constrain spawning success. / Master of Science

Globally largemouth bass Micropterus salmoides is one of the most widely introduced game fish species which has now become invasive in many countries. Well researched in its native North America, there are few studies on this species in its introduced range. This study aims to improve the understanding of the biology and ecology of M. salmoides in temperate southern Africa, where it threatens native biota and supports a popular recreational fishery. This aim was addressed by assessing the age, growth, maturity, reproductive seasonality, feeding, mortality and movement, of two M. salmoides populations from Wriggleswade (1000 ha, 723 m amsl, 32º35'S; 27º33'E) and Mankazana (35 ha, 66 m amsl, 33º09'S; 26º57'E) Dams in the Eastern Cape of South Africa. The most suitable structure for ageing M. salmoides was determined by comparing the accuracy and precision of otoliths and scales. Scales tended to underestimate the age of fish older than five years. Sectioned sagittal otoliths were the more precise structures for ageing (otoliths CV = 15.8 vs. scales CV = 21.9). The periodicity of growth zone formation was validated as annual for otoliths using both edge analysis (EA), and mark recapture of chemically tagged fish (MRCT). EA indicated one annual peak in the frequency of opaque margins between September and January using a periodic logistic regression and a binomial model linked with a von Mises distribution for circular data. MRCT showed the linear relationship between time at liberty and number of growth zones distal to the fluorescent band was not significantly different from one (slope = 0.89). Reproduction was similar to that in native and non-native populations with fish reaching age at 50% maturity at ca. two years, and length at 50% maturity at 259-290 mm FL depending on growth rate. Spawning season occurred in the spring months of August to October. The Wriggleswade Dam population reached similar ages (14 yrs) to populations in temperate North America. Growth was described using the von Bertalanffy growth equations of (Lt = 420(1-ᵉ⁻°·³³⁽ᵗ⁺°·²¹⁾) mm FL in Wriggleswade and (Lt = 641(1-ᵉ⁻°·²²⁽ᵗ⁺°·⁷⁶⁾) mm FL in Mankazana. Growth performance of both populations, described using the phi prime index, seemed to be correlated with temperature and the Wriggleswade Dam population (Φ’ = 2.8) grew similarly to those native temperate North American populations and the non-native populations of Japan and Italy. The Mankazana population had a higher growth performance (Φ’ = 2.9) compared to Wriggleswade and growth was comparable to other nonnative African populations. Both populations utilised all available food resources, with the Mankazana population being in better condition than the Wriggleswade population as a result of a more diverse diet, highly abundant food sources throughout the year, and potentially the adoption of a more conservative ambush feeding strategy. The Wriggleswade population, which was utilised by competitive anglers, showed low mortality rates (Z = 0.43 yr⁻¹), and translocated fish dispersed from the common release site, travelling an average distance of 4km over the study time of 494 days. These results indicated that M. salmoides are successful in these environments, growing at expected temperature dependant rates, maturing at two years, using all available food groups, and suffering from low mortality. It is therefore likely that they will persist in South Africa and establish where introduced.

Diverse practicing methods are evidence of the importance of applying creativity in our practice regimes. Regardless of a player's technique - traditional or modern - it must be regularly practiced and then applied. One of the most common ways to do that is through practicing technical exercises, which generally means the practice of scales, arpeggios and etudes. These exercises generally function as a warm-up regime for all musicians, but this regime doesn't necessarily provide enough reference for the player in the learning process of a new piece. Adapting exercises to address technical difficulties in a newly learned piece can provide the player with a wide range of practice methods to use, to be creative, to be more aware while practicing, and to build a solid technical foundation for the newly learned piece. Two well-known pedagogues who applied this approach are German bassist Ludwig Streicher and Czech violinist Otakar Ševčik. By implementing analytical studies and composing exercises based on the standard repertoire, Ševčik and Streicher became highly influential teachers in the 20th century. Their work serves as a model in achieving the purposes of this dissertation: the assessment of technical difficulties and compilation of a technique booklet based on six unaccompanied contemporary solo pieces written as required works for the solo competition of the International Society of Bassists' biennial convention since 2007.

During my studies at the Royal College of Music in Stockholm I have been exploring how I can develop as an improviser and as an ensemble musician. The main focus has been to use more arco playing, but also to sing unison and in harmony with the bass in order to broaden my expression. Another aim has been to compose music for my trio to implement my expanded way of performing. When I began the master’s program, I wanted to return to my roots as a classical cellist. With the help from classical teachers I was able to improve my bass technique, especially with the bow, and use that as a way to further widen my improvisation and accompany- ment skills. As a bonus, my cello playing got a boost from this work and it eventually became another important part of my artistic voice. The methods of my project have been to continuously test new ideas in my freelance work outside of KMH. I also interviewed fellow musicians to be able to reflect on whether my newly acquired knowledge and technique have had an effect on the way we make music together. In the thesis I also reflect on my inspiration from other musicians and artists and my personal philosophy not being bound to certain musical genres. Instead I want to take impressions from many different kinds of music and be open to all the different techniques in playing double bass that comes with a wide range of styles. An important result of this process is the making of the album “Arrival”, with Adam Forkelid on piano, Calle Rasmusson on drums and the Polish jazz violinist Adam Bałdych as a guest soloist. The record was released in March 2020 by the international jazz label Prophone/Naxos.

The transcription is an addition to the repertoire for brass ensemble and bass trombone. Consideration is given to the nineteenth-century orchestration treatises of Berlioz and Strauss as well as the twentieth-century texts of Erik Leidzén, Walter Piston, and Samuel Adler. The transcription process is shaped by the principles of these writers. The score is contained in the appendix.

Research on microphone choice and placement has been previously made for a variety of instruments, such as drums, vocals, and guitar, to name a few. However, in comparison, very little research has been made on the bass-cabinet. With help of the different methodologies used for previous research on electric guitar and snare drum, the optimal placement and choice of microphone for a 4x10” bass-cabinet were investigated. In a listening test, pre-recorded basslines were mixed with other instruments since it is more common to hear it in a mix of instruments rather than listening to it by itself. To make sure that the topic is not too broad, focus on the genre of rock was taken for this investigation. Both qualitative and quantitative data were collected in a set of listening tests where the subjects rated their preference for their most and least preferable basslines. The subjects were asked to describe their preference utilizing different characteristics of the stimuli. An ANOVA test provided evidence that there is a statistical difference between the preference of one microphone model at a 15 cm distance from the bass-cabinet, in the category bass with band.