Thesis (M.S.)--Oregon State University, 2010. / Printout. Includes bibliographical references (leaves 107-114). Also available on the World Wide Web.

Thesis (M.S.)--Oregon State University, 2010. / Printout. Includes bibliographical references (leaves 90-108). Also available on the World Wide Web.

Thesis (Ph.D.)--University of Central Florida, 2008. / Adviser: Graham A. J. Worthy. Includes bibliographical references.

Thesis (M.A.)--University of Hawaii at Manoa, 2004. / Includes bibliographical references (leaves 64-68). / vi, 68 leaves, bound ill. 29 cm

Thesis (Ph.D.) - University of St Andrews, May 2007.

Thesis (Ph. D.), Memorial University of Newfoundland, 1998. / Bibliography: leaves 149-175.

In this study, I characterize the maternal care patterns of humpback whales in southeast Alaska. Through a study of proximity behaviour, I show that humpbacks behave similarly to terrestrial ungulate 'followers': the cow and calf are rarely more than several body lengths apart; proximity between the cow and calf is greatest during periods of travel relative to other behaviours; and, proximity is greatest when the dive behaviour of the pair is synchronized. Unlike that observed in typical follower species, however, proximity is not found to decrease significantly as the pair's association lengthens. To account for this, I argue that the length of the observation period was insufficient to detect such a trend since maternal pairs remain together for several months after the last observations. In addition, I analyze the diving behaviour of the maternal pair to examine the potential negative consequences for the female associated with the follower tactic in humpbacks. The results suggest that several behavioural modifications are made by the cow and calf in an effort to minimize the duration of separation between the two. Ultimately, I argue that behaviour observed in humpback whales is commensurate in function with following behaviour in terrestrial ungulate followers. Humpbacks are migratory, and as in many migratory species, following behaviour provides a mechanism whereby the maternal dyad can maintain close proximity during periods of travel. Moreover, as with many follower species, humpbacks can rely upon their large size as a means of defence against offspring predation. Finally, although obvious differences exist between the habitats in which humpbacks and ungulate followers reside, arguably both are open habitats that lack the cover necessary to allow for offspring concealment.

The humpback whale is very maneuverable despite its enormous size and rigid body. This agility has been attributed to the use of its pectoral flippers, along the leading edge of which protuberances are present. The leading edge protuberances are considered by some biologists to be a form of passive flow control and/or drag reduction. Force and moment measurements along with qualitative and quantitative flow visualizations were carried out in water tunnel experiments on full-span and finite-span hydrofoil models with several different planforms and protuberance geometries. A NACA 634-021 cross-sectional airfoil profile was used for the baseline foil in all tests. Four planform geometries chosen included: a full-span set of foils which spanned the breadth of the water tunnel, a finite-span rectangular planform, a finite-span swept hydrofoil, and a scale flipper model that resembled the morphology of the humpback whale flipper. A variety of sinusoidal protuberance geometries which included three amplitudes equal to 2.5%, 5%, and 12% and wavelengths of 25% and 50% of the local chord were examined in combination with the different planform geometries. Testing included force and moment measurements and Particle Image Velocimetry (PIV) to examine the load characteristics and flow field surrounding the modified foils. Load measurements show that modified foils are capable of generating higher lift than the baseline at high angles of attack while at low angle of attack the baseline generally produces a lift coefficient equal to or greater than the modified cases. With the exception of the modified flipper model, the drag coefficients of the modified hydrofoils are either equal to or greater than their baseline counterparts. The increased drag reduces the lift-to-drag ratio. Flow visualizations show that vortical structures emanating from the shoulders of the protuberances are responsible for increased lift and drag at high angles. Cavitation tests show that modified foils cavitate in pockets behind the troughs of protuberances whereas the baseline foils produce cavitation along the entire foil span. Also, the cavitation numbers on modified hydrofoils were consistently higher than their baseline counterparts. This work shows the effect of leading edge protuberances on the aforementioned performance characteristics.

South Pacific humpback whales were devastated by commercial whaling in their Antarctic feeding areas during the 20th century. Understanding migratory connections and current abundance of these isolated breeding stocks is crucial for the allocation of historical Antarctic catches in population dynamic models used to assess current recovery. However, only a small number of migratory connections have been documented between Oceania breeding stocks within the South Pacific and feeding areas in the Antarctic. In addition, little is known about abundance of these stocks which encompass a vast oceanic region. For this thesis I first used mixed-stock analysis (MSA) to allocate migratory connections from four Antarctic feeding areas (n=142) to seven South Pacific breeding stocks (n=1,373), including four in Oceania, based on genetic marker frequencies. The use of this method was justified by the breeding stocks showing genetic differentiation at the haplotype level with an F[subscript ST] value of 0.027 (p-value <0.001). The results showed a relatively strong connection of Western Australia to Antarctic Area IV, Tonga to the border of Antarctic Area VI/I, Colombia to the Antarctic Peninsula, and a split allocation of Eastern Australia and New Caledonia to Antarctic Area V. This study provides the first population-level information supporting previous individual-based studies that humpback whale migration may not necessarily be direct north south. Next, utilizing capture-recapture methodology of unique humpback whale fluke photographs, I estimated abundance of one of the least studied Oceania breeding stocks, French Polynesia, a stock which also showed no significant migratory allocation using MSA. Taking into consideration the possible advantages of using Quality Control (QC) photographs to minimize bias in matching, estimates were generated using the complete photo catalogue and also using only photographs adhering to QC criteria. I found that the choice of using QC has an effect on the abundance generated and discuss the implications of this finding. Despite the photo catalogue used, the French Polynesia stock is estimated to number less than 1,900 individuals. Lastly, to provide additional information on the French Polynesia stock I used photo-identification to compare French Polynesia whales to whales in the Antarctic Peninsula and Strait of Magellan (Antarctic Area I), a possible migratory connection suggested by previous microsatellite genotyping. No conclusive matches were found. Although this does not discount the possibility of a few migrants traveling between these regions it does indicate the Antarctic Peninsula and the Strait of Magellan are not primary feeding areas of French Polynesia. This new information regarding abundance and migration of French Polynesia whales is important for the Comprehensive Assessment of Southern Hemisphere humpback whales. This document is currently being completed as the International Whaling Commission considers the next critical steps in recovery for Oceania humpback whales stocks. / Graduation date: 2010

Humpback whales (Megaptera novaeangliae) belong baleen whales. They migrate between high-latitude summer feeding regions and low-latitude wintering regions where calving and make place.There were 1~60 humpback whales whaled every year during 1920~1967 in southern Taiwan. However, only a few sights were recorded in the past twenty years. A male humpback whale was sighted on the east coast of Taiwan in March, 2000. His songs recorded during between three-day tailing were analysed. There were five themes and nine units in the songs, a complete song duration lasted about 14.2 minutes. The maximal sound pressure level was 189.6 dB (n=32, SEM =2.81). The acoustic characters (i.e., signal duration, time between two signals, theme duration, fundamental frequency) of the songs were not significant different. A visual comparison of the spectrograms of the sound units from this particalar whale with those northwest Pacific Ocean showed similarity. This individual was a member of the population in the northwest Pacific Ocean. This conclusion was also supported by the result of Photo-ID of its fluke. Ceatceans live in the water and develop the special model to produce sounds. There are two kinds of communicative signals: pulses and whistles. These two signals were characters of phylogenetic relationship and the outgroup was red deer. There were two monophyletic groups. Evolution of communicative signals in cetaceans was whistle existent and added the pulses signals. Last, the whistles lost and only with pulses. The fumctions of pulse signals in communication was unknown in delphinidae. Sperm whales, pygmy sperm whales, dwarf sperm whales, Baird¡¦s beaked whales and Hector¡¦s dolphins were only use pulse signals. The reason of this change was unclear.