Wildlife forensics: "supervised" assignment testing can complicate the association of suspect cases to source populations.

Forensic science techniques are an important component of investigations for wildlife-related offences. In particular, DNA analyses can be used to characterize several attributes of biological evidence including sex, individual and species identification. Additionally, genetic assignment testing has enabled forensic biologists to identify the local population from which an individual may have originated. This technique has proved useful in situations where animals have been illegally harvested from areas/populations where hunting is prohibited. For this report, we used individual-based clustering (IBC), in the program Structure 2.2, under both "supervised" and "unsupervised" approaches to assess whether three suspected, illegally harvested moose originated from an endangered population. Atypical circumstances, with Nova Scotia having two moose sub-species in its jurisdiction, enabled strong IBC assignment testing results to determine the source population of the suspected samples. We found differences between the "unsupervised" and "supervised" modeling approaches to define genetic structure among the a priori characterized populations in our data set. Our findings illustrate the fact that individual clustering assignment tests can assist wildlife forensic cases to identify the source population of illegally harvested animals. However, the accuracy of results are highly dependant on the model choice used to define genetic clusters, as well as on the availability of a thorough database of samples throughout the managed area to accurately identify all genetic populations. Further, it is clear from our analyses that political jurisdictions do not accurately reflect isolated populations and we recommend using unsupervised IBC modeling for biological accuracy.

Effects of neonatal oxytocin treatment on aggression and neural activities in mandarin voles.

Neonatal manipulation of oxytocin (OT) has long-term effects on behavior and physiology. Here we test the hypothesis that neonatal OT treatment can affect the subsequent expression of intrasexual aggression partly by reprogramming the neural activities of relevant brain regions. To test this hypothesis, mandarin voles (Lasiopodomys mandarinus) received OT or isotonic saline treatment within 24 h of birth. At about 75 days of age, aggressive behaviors and Fos expression in different brain regions were tested. The results indicate that the (1) level of intrasexual aggression was higher and other social contact was lower in SAL-treated sexually naïve males than in females and; (2) OT-treated females showed a greater increase in aggressive behaviors and Fos expression only after exposure to a male than SAL-treated females, but there were no significant changes in aggressive behaviors in males. These results demonstrate a sexual difference in aggression, and that neonatal exposure to OT may increase aggression in female mandarin voles. These effects may be based on changes in neural activities of relevant brain regions including the bed nucleus of the stria terminalis (BNST), lateral septal nucleus (LS), medial preoptic area (MPOA), the paraventricular nucleus of the hypothalamus (PVN), supraoptic nucleus (SON), mediodorsal thalamic nucleus (MD), ventromedial nucleus of hypothalamic (VMH), the medial amygdala (MeA) and central amygdala (CeA).

Population genetic structure and the effect of founder events on the genetic variability of moose, Alces alces, in Canada.

Moose, Alces alces, occur naturally throughout most of Canada but successful introductions of known numbers of animals have been made to the islands of Newfoundland and Cape Breton. Five microsatellite loci were used to investigate the population genetic structure and any change in genetic variability due to founder events of moose in Canada. Comparisons of allele frequencies for moose from 11 regions of the country suggested that there are at least seven genetically distinct populations (P < 0.05) in North America, namely Alberta, eastern Ontario, New Brunswick, Cape Breton, Labrador, western Newfoundland, and the Avalon Peninsula of Newfoundland. The average population heterozygosity was approximately 33% (range from 22 to 41%). UPGMA analysis of Nei's genetic distances produced phenograms similar to what would be expected when geographical location and population history are considered. The loss of heterozygosity due to a single founder event (n = 3; two introductions and a natural colonization) ranged from 14 to 30%, and the cumulative loss of heterozygosity due to two successive founder events (an introduction followed by a natural colonization) was 46%. In these examples loss of genetic variability has not been associated with any known phenotypic deviances, suggesting that populations may be established from a small number of founders. However, the viability of these founded populations over evolutionary timescales cannot be determined and is highly dependent upon chance.