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Species -area relationships are the product of many ecological processes and their interactions. Explanations for the species -area relationship (SAR) have focused on separating putative niche-based mechanisms that correlate with area from sampling eff ects caused by patches with more individuals containing more species than patches with fewer individuals. We tested the hypothesis that SARs in breeding waterfowl communities are caused by sampling eff ects (i.e. random placement from the regional species pool). First, we described observed SARs and patterns of species associations for fourteen species of ducks on ponds in prairie Canada. Second, we used null models, which randomly allocated ducks to ponds, to test if observed SARs and patterns of species associations diff ered from those expected by chance. Consistent with the sampling eff ects hypothesis, observed SARs were accurately predicted by null models in three diff erent years and for diving and dabbling duck guilds. Th is is the fi rst demonstration that null models can predict SARs in waterbirds or any other aquatic organisms. Observed patterns of species association, however, were not well predicted by null models as in all years there was less observed segregation among species (i.e. more aggregation) than under the random expectation, suggesting that intraspecifi c competition could play a role in structuring duck communities. Taken together, our results indicate that when emergent properties of ecological communities such as the SAR appear to be caused by random processes, analyses of species associations can be critical in revealing the importance of niche-based processes (e.g. competition) in structuring ecological communities.

2005. Dietary calcium limits size and growth of nestling tree swallows Tachycineta bicolor in a non-acidified landscape. Á/ J. Avian Biol. 36: 127 Á/134.Much previous research has focussed on the role of food supply in determining the growth and the survival of avian offspring. More recently, acid deposition in some ecosystems has demonstrated that in addition to energy, birds also need to acquire sufficient nutrients such as calcium to be successful. Whether procurement of adequate levels of calcium can limit reproductive success in areas that have not been impacted by acid rain remains equivocal. We tested whether calcium affected reproductive success of tree swallows Tachycineta bicolor by feeding extra calcium to nestlings during the brood-rearing period. Our manipulation did not enhance the survival of offspring, however, provisioning of extra calcium resulted in nestlings showing enhanced rates of growth of mass (all nests) and of ninth primary flight feathers (nests with after-second year female parents), compared to control nestlings. Calcium supplementation also resulted in nestlings having longer feathers and tarsi at age 16 days, and there was evidence that some nestlings receiving extra calcium were heavier at 16 days old. As offspring that have faster growth, or that are in good condition at fledging, often survive better after leaving the nest, these results suggest that calcium availability can limit fitness. Our results are noteworthy because our experiment was conducted in an area with abundant soil calcium where acid deposition has not occurred. The role of calcium in limiting the reproductive performance of avian species may therefore be more pervasive than previously thought.

Defining and identifying changes to seasonal ranges of migratory species is required for effective conservation. Historic sightings of migrating whooping cranes (Grus americana) have served as sole source of information to define a migration corridor in the Great Plains of North America (i.e., Canadian Prairies and United States Great Plains) for this endangered species. We updated this effort using past opportunistic sightings from 1942–2016 (n = 5,055) and more recent (2010–2016) location data from 58 telemetered birds (n = 4,423) to delineate migration corridors that included 50%, 75%, and 95% core areas. All migration corridors were well defined and relatively compact, with the 95% core corridor averaging 294 km wide, although it varied approximately ±40% in width from 170 km in central Texas to 407 km at the international border of the United States and Canada. Based on historic sightings and telemetry locations, we detected easterly movements in locations over time, primarily due to locations west of the median shifting east. This shift occurred from northern Oklahoma to central Saskatchewan at an average rate of 1.2 km/year (0.3–2.8 km/year). Associated with this directional shift was a decrease in distance of locations from the median in the same region averaging -0.7 km/year (-0.3–-1.3 km/year), suggesting a modest narrowing of the migration corridor. Changes in the corridor over the past 8 decades suggest that agencies and organizations interested in recovery of this species may need to modify where conservation and recovery actions occur. Whooping cranes showed apparent plasticity in their migratory behavior, which likely has been necessary for persistence of a wetland-dependent species migrating through the drought-prone Great Plains. Behavioral flexibility will be useful for whooping cranes to continue recovery in a future of uncertain climate and land use changes throughout their annual range.

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