We examined nest- and roost-burrow characteristics from a declining population of burrowing owls (Athene cunicularia (Molina, 1782)) in Saskatchewan. Between 1992 and 2003, 84% of the 584 nests we found were in grassland pastures, even though these pastures constituted only 7% of the potentially available nesting area within our study area. In contrast, less than 3% of nests were in crop fields, despite these fields comprising 90% of the potentially available area. Within grassland pastures, owls selected nest burrows in areas with a higher density of burrows within 75 m (11.1 burrows/ha) compared with non-nest burrows of similar dimensions (5.6 burrows/ha). Richardson's ground squirrels (Spermophilus richardsonii (Sabine, 1822)) and badgers (Taxidea taxus (Schreber, 1777)) are the primary excavators of suitable nesting burrows in prairie Canada. In our study area, burrowing owls chose to nest and roost in badger-sized burrows, selecting those with taller tunnel entrances and soil mounds relative to unused burrows. We suggest that management for burrowing owl nesting habitat in Canada should consider the owls' avoidance of crop fields and their preference for grassland pastures. Managers should also consider the owls' apparent preference for nesting in areas of high burrow densities and their selection of badger-sized burrows for nesting and roosting.

An increasing body of studies of widely distributed, high latitude species shows a variety of refugial locations and population genetic patterns. We examined the effects of glaciations and dispersal barriers on the population genetic patterns of a widely distributed, high latitude, resident corvid, the gray jay (Perisoreus canadensis), using the highly variable mitochondrial DNA (mtDNA) control region and microsatellite markers combined with species distribution modeling. We sequenced 914 bp of mtDNA control region for 375 individuals from 37 populations and screened seven loci for 402 individuals from 27 populations across the gray jay range. We used species distribution modeling and a range of phylogeographic analyses (haplotype diversity, ΦST, SAMOVA, F ST, Bayesian clustering analyses) to examine evolutionary history and population genetic structure. MtDNA and microsatellite markers revealed significant genetic differentiation among populations with high concordance between markers. Paleodistribution models supported at least five potential areas of suitable gray jay habitat during the last glacial maximum and revealed distributions similar to the gray jay's contemporary during the last interglacial. Colonization from and prolonged isolation in multiple refugia is evident. Historical climatic fluctuations, the presence of multiple dispersal barriers, and highly restricted gene flow appear to be responsible for strong genetic diversification and differentiation in gray jays.

The genetic impact of barriers and Pleistocene glaciations on high latitude resident species has not been widely investigated. The Clark’s nutcracker is an endemic North American corvid closely associated with Pinus-dominated forests. The nutcracker’s encompasses known barriers to dispersal for other species, and glaciated and unglaciated areas. Clark’s nutcrackers also irruptively disperse long distances in search of pine seed crops, creating the potential for gene flow among populations. Using the highly variable mitochondrial DNA control region, seven microsatellite loci, and species distribution modeling, we examined the effects of glaciations and dispersal barriers on population genetic patterns and population structure of nutcrackers. We sequenced 900 bp of mitochondrial control region for 169 individuals from 15 populations and analysed seven polymorphic microsatellite loci for 13 populations across the Clark’s nutcracker range. We used species distribution modeling and a range of phylogeographic analyses to examine evolutionary history. Clark’s nutcracker populations are not highly differentiated throughout their range, suggesting high levels of gene flow among populations, though we did find some evidence of isolation by distance and peripheral isolation. Our analyses suggested expansion from a single refugium after the last glacial maximum, but patterns of genetic diversity and paleodistribution modeling of suitable habitat were inconclusive as to the location of this refugium. Potential barriers to dispersal (e.g. mountain ranges) do not appear to restrict gene flow in Clark’s nutcracker, and postglacial expansion likely occurred quickly from a single refugium located south of the ice sheets.

Fledgling birds are notoriously difficult to find and capture because of their cryptic behavior. As a result, researchers usually affix transmitters to nestlings to study aspects of post-fledging ecology. However, parents may attempt to remove nestling transmitters, which could negatively impact nestlings. We attached radio-transmitters to 95 Sprague's Pipit (Anthus spragueii) nestlings using a modified Rappole and Tipton leg harness. Within 1-2 days after transmitter attachment, we recorded six cases of parents removing transmitters from nestlings and depositing the transmitters outside the nest. At one of these nests, we videotaped parents pecking and pulling at nestlings that had transmitters and also dragging a nestling out of the nest by the transmitter. Of 12 video-monitored nests where we attached transmitters to nestlings, 33% had cases of parents attempting to remove transmitters by pecking and pulling at nestlings. Our observations highlight the need to closely monitor nestlings with transmitters so that researchers have the opportunity to reattach transmitters should parents remove them and to monitor the health of nestlings. Videomonitoring nests could also help to identify any unseen, negative impacts on nestlings due to transmitter attachment.

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