A total of 9 brushtail possums (Trichosurus vulpecula) were trained to perform a two-manipulanda, conditional discrimination task. The possums learned to press a right lever in the presence of a tone (80 dB(A)) during tone-on trials, and a left lever in the absence of the tone on tone-off trials. Overall sessions of 11 conditions contained tone frequency between 100 Hz and 35 kHz were tested. Each condition contained training and then probe sessions. In training sessions, the possums were presented with tone-on and tone-off trials, pseudo-randomly. Once the possums responded with over 90% accuracy for five consecutive sessions, then probe sessions were introduced. Probe sessions were similar to the training sessions, except that the tone intensity for tone-on trials was reduced by 8 dB(A) across blocks of 20 trials until their response accuracy in a block fall below 60% or reached 24 dB(A). Data were analysed using overall percentages correct and log d analysis. Both measures indicated that overall response accuracy decreased for all possum as tone intensity reduced. Based on these data analyses, threshold values were calculated using the criterions at 75% correct and a log d of 0.48. The threshold values for each possum and across all possums were plotted as a function of the tone frequency to produce an audiogram. A curvilinear regression was fitted for each threshold values. The functions of both measures were very similar. Both audiograms showed that the possums could hear the tones between 100 Hz and 35 kHz, and were most sensitive to tones between 15 and 20 kHz. This experiment involved many difficulties with producing and measuring tones especially outside of human hearing range. Due to these difficulties, several problems and concerns were raised during the experiment, these were discussed in this study and also recommendations for future research were then presented.

This thesis is about making inference on the host status of feral ferrets in New Zealand for Mycobacterium bovis, the aetiological agent of bovine tuberculosis. The central question addressed is whether the rate of intra-specific transmission of M. bovis among ferrets is sufficient for the disease to persist in ferret populations in the absence of external, non-ferret sources of infection (inter-specific transmission). The question is tackled in three parts�firstly using model selection to identify suitable models for estimating the force of M. bovis infection in ferret populations; secondly applying statistical hypothesis testing to the results of planned manipulative field experiments to test the relationship between M. bovis infection in brushtail possums and that in ferrets; and thirdly using modelling to estimate intra-specific disease transmission rates and the basic reproductive rate (Ro) of M. bovis infection in ferrets. The model selection approach clearly identified the hypothesis of oral infection related to diet was, as modelled by a constant force of infection from the age of weaning, the best approximation of how M. bovis infection was transmitted to ferrets. No other form of transmission (e.g., during fighting, mating, or routine social interaction) was supported in comparison. The force of infection (λ) ranged from 0.14 yr-1 to 5.77 yr-1, and was significantly higher (2.2 times) in male than female ferrets. Statistical hypothesis testing revealed transmission of M. bovis to ferrets occurred from both brushtail possums and ferrets. The force of M. bovis infection in ferrets was reduced by 88% (λ=0.3 yr-1 vs. λ=2.5 yr-1) at sites with reductions in the population density of sympatric brushtail possum populations. A smaller decline in the force of infection resulting from the lethal cross-sectional sampling of the ferret populations was also demonstrated. The modelling approach estimated the basic reproductive rate (Ro) of M. bovis infection in ferrets in New Zealand to vary from 0.17 at the lowest population density (0.5 km-2) recorded to 1.6 at the highest population density (3.4 km-2) recorded. The estimates of Ro were moderately imprecise, with a coefficient of variation of 76%. Despite this imprecision, the Ro for M. bovis infection in ferrets was significantly less than unity for all North Island sites surveyed. Hence it is inferred ferrets are spillover hosts (0<Ro<1) for M. bovis infection in these environments. That is, M. bovis infection will progressively disappear from these ferret populations if the source of inter-specific transmission is eliminated. The estimates of Ro for M. bovis infection in South Island ferret populations were above one (the level required for disease establishment) for a number (5/10) of populations, though the imprecision made it impossible to ascertain whether Ro was significantly greater than one. The estimated threshold population density (Kt) for disease establishment was 2.9 ferrets km-2. It is inferred that, given sufficient population density (>Kt), the rate of intra-specific transmission of M. bovis among ferrets is sufficient for the disease to establish in ferrets in the absence of interspecific transmission. In these areas, ferrets would be considered maintenance hosts for the disease. Active management (e.g., density reduction or vaccination) of ferrets would be required to eradicate M. bovis from ferret populations in these areas, in addition to the elimination of sources of inter-specific transmission, particularly brushtail possums.