An observational analysis of Canada Jay (Perisoreus canadensis) foraging and caching ecology in Denali National Park and Preserve, Alaska, USA

Arctic and subarctic wildlife are among the most vulnerable species to climate change. Canada Jays (Perisoreus canadensis (Linnaeus, 1776)) are generalist residents of northern boreal forests and scatter-hoard food to insulate against food scarcity during winter. Unlike most scatter-hoarders, however, Canada Jays primarily cache perishable food, rendering their caches more susceptible to climate change induced degradation and loss. Here we use a mostly noninvasive approach to document Canada Jay foraging ecology among a population in interior Alaska, USA, including the types of food acquired, foraging and caching rates, and cache longevity and loss. We also tested for associations between foraging and caching rates with reproductive metrics to assess possible relationships among food and productivity. We found that Canada Jays have a varied diet that changed seasonally, and responded to a record-setting warm spring by directing foraging efforts away from cache recovery and towards the emergence of fresh food. We did not find evidence for relationships between foraging and caching rate with reproductive output, possibly owing to small sample sizes. We found that caches were recovered quickly (<4 weeks) and frequently lost to conspecific and heterospecific competitors. Our study suggests that Canada Jays may be better poised to respond to changes in cache integrity and food availability than has been previously recognized.

No evidence for future planning in Canada jays ( Perisoreus canadensis )

In the past 20 years, research in animal cognition has challenged the belief that complex cognitive processes are uniquely human. At the forefront of these challenges has been research on mental time travel and future planning in jays. We tested whether Canada jays ( Perisoreus canadensis ) demonstrated future planning, using a procedure that has produced evidence of future planning in California scrub-jays. Future planning in this procedure is caching in locations where the bird will predictably experience a lack of food in the future. Canada jays showed no evidence of future planning in this sense and instead cached in the location where food was usually available, opposite to the behaviour described for California scrub-jays. We provide potential explanations for these differing results adding to the recent debates about the role of complex cognition in corvid caching strategies.

Investigating factors that set the lower elevational limit of Canada jays (Perisoreus canadensis) on Vancouver Island

The biotic and abiotic factors responsible for determining ranges of most species are poorly understood. The Canada jay (Perisoreus canadensis Linnaeus, 1766) relies on perishable cached food for over-winter survival and late-winter breeding and the persistence of cached food could be a driver of range limits. We confirmed that the Canada jay’s lower elevational limit on Vancouver Island, British Columbia, matches that of the subalpine zone (900 m) and then conducted simulated caching experiments to examine the influence of antimicrobial properties of subalpine tree species (biotic) and of temperature (abiotic) on the preservation of cached food. We found that two high-elevation species, Yellow cedar (Callitropsis nootkatensis D. Don, D.P. Little) and Amabilis fir (Abies amabilis Douglas ex J. Forbes) preserved cached blueberries and chicken flesh better than other trees but they also occurred well below the lower limit of Canada jays. The effect of temperature was similarly unclear; while food cached at 1150 m retained 17 % more mass than food cached at 550 m, there was no difference in percent mass remaining of food placed 70 m above, versus 120 m below, the Jay lower elevational limit. Thus we were unable to provide definitive evidence that either of the proposed abiotic or biotic factors was responsible for setting the Canada jay lower elevational limit of resident Canada jays.

A bird that changes colour without moulting: how the wîskicâhk (Canada Jay, Perisoreus canadensis) tricked the taxonomists

Avian and mammalian colours are thought to be constant in life and in museum specimens, but several early 20th-century taxonomists singled out the Canada Jay (Perisoreus canadensis (Linnaeus, 1766)) as having unstable feather pigments and warned against using old museum specimens for taxonomic purposes. One such error was Brisson’s (1760) original naming of the species as “the Brown Jay of Canada”. Another was Ridgway’s (1899) naming of the “Gray Jay” as a new subspecies, Perisoreus (canadensis) griseus, through inappropriate comparison of fresh grey specimens with old brown ones. We discovered that browning of initially grey plumage also occurs between annual moults in living individuals of the Canada Jay’s Pacific morphotype. We documented this change using photographs and re-sightings of colour-banded individuals and through spectral analysis of year-old (brown) and incoming (grey) rectrices collected from the same moulting individuals. To assess the distribution of this colour change, we compared September vs. May eBird photographs from across North America. We showed that seasonal colour change is normal in the Pacific morphotype but rare in the two other morphotypes. Collectively, these data have important implications for the taxonomy of the Canada Jay and are a cautionary tale for taxonomists studying animal colouration.

New avian breeding records for Kugluktuk, Nunavut

New breeding records for 10 species of tundra and boreal nesting birds were documented near the community of Kugluktuk (Nunavut, Canada) over the course of the 2015 and 2016 breeding seasons and incidentally in 2017 and 2018. These species include American Wigeon (Mareca americana), Mallard (Anas platyrhynchos), Northern Shoveler (Anas clypeata), Green-winged Teal (Anas carolinensis), Greater Scaup (Aythya marila), Say’s Phoebe (Sayornis saya), Canada Jay (Perisoreus canadensis), Greycheeked Thrush (Catharus minimus), Yellow-rumped Warbler (Setophaga coronata), and Dark-eyed Junco (Junco hyemalis). Previously unpublished breeding evidence for Bald Eagle (Haliaeetus leucocephalus) is also discussed along with suspected breeding of Barn Swallow (Hirundo rustica), Bohemian Waxwing (Bombycilla garrulus), White-throated Sparrow (Zonotrichia albicollis), and Pine Grosbeak (Pinicola enucleator). These records represent the first described breeding occurrences for these species in the Kitikmeot region, or new records for the mainland of Nunavut. A lack of historical ornithological survey effort in this area has likely led to the diversity of these previously unrecorded breeding observations. These results highlight the need to increase geographic coverage of bird surveys in northern Canada to more accurately delineate the northern limit of breeding ranges and suggest that further formal survey effort will undoubtedly lead to additional new breeding records.

A test of the predator avoidance hypothesis to explain delayed onset of communal breeding

A neglected question in the study of communal breeding concerns why alloparental behaviour begins at variously late stages in the breeding cycle. In group-living corvids, the delay tends to be longer in species that are small and (or) typically have only a small nonbreeder complement. This pattern has been attributed to the relatively poor defensive capabilities of such species and their consequently greater need to minimize predator-attracting traffic to the nest or fledglings. We tested this predator avoidance hypothesis with the Canada Jay (Perisoreus canadensis (Linnaeus, 1766)), a species in which the feeding of young by any nonbreeders in the family group is delayed until the fledgling period. We reasoned that, on Anticosti Island, Quebec (Canada), in the absence of squirrels and other nest predators, nonbreeders might be permitted to feed nestlings as well as fledglings, and that breeders might feed nestlings more frequently (with smaller food loads) than on the mainland. We found no evidence for either prediction and thus no support for the predator avoidance hypothesis but suggest that Anticosti Canada Jays may have had insufficient time to evolve behaviour more appropriate for their predator-free environment. Secondarily, we confirmed that in all observed instances, the nonbreeders were offspring of the breeding pair from previous years and that they therefore failed to provision nestlings in spite of an apparent genetic interest to do so.