Although Icelandic and Norwegian killer whales are thought to have been in contact prior to the collapse of the herring stock in the 1960s, the Northeast Atlantic killer whales currently seem to show high site fidelity. So far, photoidentification data have suggested movement of a few individuals between East Iceland and North Scotland, and two calls have been shown to be shared by the Icelandic and Norwegian populations. Based on previous and newly analysed call samples, the aim of this study was to describe the geographic variation in the vocal repertoire of the Northeast Atlantic killer whales. Recordings have been conducted off Southwest Iceland in the summers 2004, 2008 and 2009 using sound recording tags attached using suction cups (Dtags), a 4-element vertical hydrophone array and a 2-element towed hydrophone array. From the 57 hours of recording analysed, 1742 calls were classified. In total, 56 distinct call categories composed of 35 call types and 31 subtypes were identified. This discrete call repertoire contained less biphonic calls but more calls composed of buzzes and/or clicks than the Norwegian repertoire. The reasons for these differences remain unknown. One Icelandic call subtype was defined as a compound call, a type of call that is common in the Norwegian population. The comparison of the different vocal repertoires of Northeast Atlantic showed four good or likely call matches in herring-eating killer whales (one between Southwest Iceland and Shetland, one between East Iceland and Norway, and two between Shetland and Norway). No matches were found between Southwest Iceland and East Iceland. I suggest that the four shared calls are most likely to have come from a common ancestral pod and have been transmitted through vocal learning. Over time, geographic isolation of the groups induced by changes in the migratory patterns of the herring might have been accompanied by divergence in their call repertoires.

The acoustic sense is vital to all life processes for whales. It defines their ‘active space’, and the extent and nature of interactions with their surroundings. Yet, we are still learning the basics of most species’ acoustic behaviours and vocal repertoires. The ecology of gray whales (Eschrichtius robustus) is well known, however vocal behaviours are not well described outside of breeding lagoons. Bottom-stationed acoustic monitoring devices were deployed in Clayoquot Sound, west coast Vancouver Island to explore acoustics use outside of these areas. During migration the use of low frequency moan calls are prevalent, perhaps for group cohesion, with lead whales guiding followers. During the summer more inter-group calls (knocks, upsweeps) are employed. Here I explored the use of ‘motherese’ calls between cow-calf pairs, and how this may mirror the weaning process. Photoperiod, increased ambient noise, threat perception, and vessel and aircraft presence elicited acoustic responses. Calling was also altered by social, behavioural, and physiological state. These results begin to show gray whales to be acoustically sensitive, with highly nuanced vocalising behaviours. Acoustic methods afford monitoring at times and in places that would otherwise be impossible, and lends themselves to the study of rare or cryptic species. Ocean gliders with passive acoustic capacity were used to explore deep-coastal and shelf-break waters for large whale species. Humpback whales (Megaptera novaeangliae) were common on the shelf, whereas calls from fin (Balaenoptera physalus), blue (Balaenoptera musculus), sperm (Physeter macrocephalus), and possibly sei whales (Balaenoptera borealis) were heard in more offshore locations. Concurrent habitat data steams help establish area use and importance to these species. The surveys focus on submarine canyons that are thought to aggregate prey. Calls denote whale presence, whereas call type may suggest behaviour and habitat use. Calls described for feeding and breeding were heard for fin and blue whales, with distinct temporal distribution. Acoustic techniques complement other ecological methods and can fill existing knowledge gaps in whale life histories. It can also help quantify the effect of human activities on whale populations and ocean soundscapes. These findings will inform management actions. I provide examples of management links to acoustic-ecological research. / Graduate

Acoustic communication in anurans plays a critical role in species recognition, defending territories and resources, and finding a mate. Anurans use a number of different call note types to communicate, from which the most notable are advertisement- and aggression calls. Optimum weather conditions are a precursor to the commencement of the breeding season for all frog species and their calling behaviour is therefore readily influenced by atmospheric conditions. Male frogs within a chorus also tend to call from territories within a specific range of distances from one another. The objectives of this study were to 1) determine a possible context in which call note types are produced, 2) to determine the effect of atmospheric conditions on calling behaviour and 3) to determine the spacing distances between males and females in a chorus of Queckett’s River Frog (Amietia quecketti). Pre-recorded note types were used in a playback experiment to determine a context for elicited responses. A context was derived for six of the responses. Advertisement (clicks and whines), aggression (creaks), encounter (tonal notes), territorial (whine-tonal notes), and release calls (squeaks) were described. Calls and atmospheric conditions were recorded and correlated for an entire breeding season. Water temperature, wind speed, humidity and barometric pressure had a significant effect on calling intensity. As water temperature decreased calling intensity increased, while increased wind temperature led to increased calling intensity. Amietia quecketti calls from the water, explaining the effect while increased wind speed decreases water temperature and can carry sound further. Both humidity and barometric pressure showed increased calling intensity only at specific levels. Humidity and barometric pressure have a direct effect on one another, which most likely causes the correlation between calling intensity and both these variables. In this study A. quecketti was shown to have breeding ponds for males and resting ponds and positions for non-gravid females. This prevents unwanted or unnecessary amplexus. Males showed much smaller and less variable territory sizes than females. This is most likely because males have a small range of optimal spacing distance while females move towards and away from males. The presence of vegetation resulted in smaller territories. This is possibly because smaller males act as satellite males and cannot be seen by larger males in vegetation. The size of males did not affect territory size. Males have a specific inter-male spacing distance regardless of size. / MSc (Environmental Sciences), North-West University, Potchefstroom Campus, 2015

Acoustic communication in anurans plays a critical role in species recognition, defending territories and resources, and finding a mate. Anurans use a number of different call note types to communicate, from which the most notable are advertisement- and aggression calls. Optimum weather conditions are a precursor to the commencement of the breeding season for all frog species and their calling behaviour is therefore readily influenced by atmospheric conditions. Male frogs within a chorus also tend to call from territories within a specific range of distances from one another. The objectives of this study were to 1) determine a possible context in which call note types are produced, 2) to determine the effect of atmospheric conditions on calling behaviour and 3) to determine the spacing distances between males and females in a chorus of Queckett’s River Frog (Amietia quecketti). Pre-recorded note types were used in a playback experiment to determine a context for elicited responses. A context was derived for six of the responses. Advertisement (clicks and whines), aggression (creaks), encounter (tonal notes), territorial (whine-tonal notes), and release calls (squeaks) were described. Calls and atmospheric conditions were recorded and correlated for an entire breeding season. Water temperature, wind speed, humidity and barometric pressure had a significant effect on calling intensity. As water temperature decreased calling intensity increased, while increased wind temperature led to increased calling intensity. Amietia quecketti calls from the water, explaining the effect while increased wind speed decreases water temperature and can carry sound further. Both humidity and barometric pressure showed increased calling intensity only at specific levels. Humidity and barometric pressure have a direct effect on one another, which most likely causes the correlation between calling intensity and both these variables. In this study A. quecketti was shown to have breeding ponds for males and resting ponds and positions for non-gravid females. This prevents unwanted or unnecessary amplexus. Males showed much smaller and less variable territory sizes than females. This is most likely because males have a small range of optimal spacing distance while females move towards and away from males. The presence of vegetation resulted in smaller territories. This is possibly because smaller males act as satellite males and cannot be seen by larger males in vegetation. The size of males did not affect territory size. Males have a specific inter-male spacing distance regardless of size. / MSc (Environmental Sciences), North-West University, Potchefstroom Campus, 2015