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Christopher A. Nicolai

Publications and source records attributed to Christopher A. Nicolai.

4 recordsLinked to original sources

Variation in body mass dynamics among sites in Black Brant Branta bernicla nigricans supports adaptivity of mass loss during moult

Birds employ varying strategies to accommodate the energetic demands of moult, one important example being changes in body mass. To understand better their physiological and ecological significance, we tested three hypotheses concerning body mass dynamics during moult. We studied Black Brant in 2006 and 2007 moulting at three sites in Alaska which varied in food availability, breeding status and whether geese undertook a moult migration. First we predicted that if mass loss during moult were simply the result of inadequate food resources then mass loss would be highest where food was least available. Secondly, we predicted that if mass loss during moult were adaptive, allowing birds to reduce activity during moult, then birds would gain mass prior to moult where feeding conditions allowed and mass loss would be positively related to mass at moult initiation. Thirdly, we predicted that if mass loss during moult were adaptive, allowing birds to regain flight sooner, then across sites and groups, mass at the end of the flightless period would converge on a theoretical optimum, i.e. the mass that permits the earliest possible return to flight. Mass loss was greatest where food was most available and thus our results did not support the prediction that mass loss resulted from inadequate food availability. Mass at moult initiation was positively related to both food availability and mass loss. In addition, among sites and years, variation in mass was high at moult initiation but greatly reduced at the end of the flightless period, appearing to converge. Thus, our results supported multiple predictions that mass loss during moult was adaptive and that the optimal moulting strategy was to gain mass prior to the flightless period, then through behavioural modifications use these body reserves to reduce activity and in so doing also reduce wing loading. Geese that undertook a moult migration initiated moult at the highest mass, indicating that they were more than able to compensate for the energetic cost of the migration. Because Brant frequently change moult sites between years in relation to breeding success, the site-specific variation in body mass dynamics we observed suggests individual plasticity in moult body mass dynamics.

Alaska

Mate loss affects survival but not breeding in black brant geese

For birds maintaining long-term monogamous relationships, mate loss might be expected to reduce fitness, either through reduced survival or reduced future reproductive investment. We used harvest of male brant during regular sport hunting seasons as an experimental removal to examine effects of mate loss on fitness of female black brant (Branta bernicla nigricans; hereafter brant). We used the Barker model in program MARK to examine effects of mate loss on annual survival, reporting rate, and permanent emigration. Survival rates decreased from 0.847 ± 0.004 for females who did not lose their mates to 0.690 ± 0.072 for birds who lost mates. Seber ring reporting rate for females that lost their mates were 2 times higher than those that did not lose mates, 0.12 ± 0.086 and 0.06 ± 0.006, respectively, indicating that mate loss increased vulnerability to harvest and possibly other forms of predation. We found little support for effects of mate loss on fidelity to breeding site and consequently on breeding. Our results indicate substantial fitness costs to females associated with mate loss, but that females who survived and were able to form new pair bonds may have been higher quality than the average female in the population.

Behavioral Ecology

Carryover effects associated with winter location affect fitness, social status, and population dynamics in a long-distance migrant

We used observations of individually marked female black brant geese (Branta bernicla nigricans; brant) at three wintering lagoons on the Pacific coast of Baja California—Laguna San Ignacio (LSI), Laguna Ojo de Liebre (LOL), and Bahía San Quintín (BSQ)—and the Tutakoke River breeding colony in Alaska to assess hypotheses about carryover effects on breeding and distribution of individuals among wintering areas. We estimated transition probabilities from wintering locations to breeding and nonbreeding by using multistratum robust-design capture-mark-recapture models. We also examined the effect of breeding on migration to wintering areas to assess the hypothesis that individuals in family groups occupied higher-quality wintering locations. We used 4,538 unique female brant in our analysis of the relationship between winter location and breeding probability. All competitive models of breeding probability contained additive effects of wintering location and the 1997–1998 El Niño–Southern Oscillation (ENSO) event on probability of breeding. Probability of breeding in non-ENSO years was 0.98 ± 0.02, 0.68 ± 0.04, and 0.91 ± 0.11 for females wintering at BSQ, LOL, and LSI, respectively. After the 1997–1998 ENSO event, breeding probability was between 2% (BSQ) and 38% (LOL) lower than in other years. Individuals that bred had the highest probability of migrating the next fall to the wintering area producing the highest probability of breeding.

American Naturalist

Annual survival and site fidelity of northern pintails banded on the Yukon-Kuskokwim Delta, Alaska

We banded northern pintails (Anas acuta; n = 13,645) at a single site on the Yukon-Kuskokwim Delta (YKD), Alaska, USA, from 1990 to 2001. We used recaptures from our site in combination with hunter recoveries to model annual survival, recovery rates, and fidelity to our capture location. Most recoveries (>90%) occurred in the Pacific Flyway with 64% reported from California's Central Valley. Our top candidate models allowed survival to vary by sex but not by age or year. Estimated annual survival was 77.6% (95% CI: 73.9-81.0%) for males and 60.2% (95% CI: 53.2-67.0%) for females. Reporting rates varied by age, sex, and year; estimates for adult males exceeded those for adult females by 3.5 times. Within sexes, reporting rates of hatch-year pintails exceeded those of adults. Estimated recovery rates were considerably lower than those estimated during the 1950s-1970s for winter banded pintails (Hestbeck 1993b), but there were no differences in survival rates. This suggests that changes in harvest regulations may not have influenced annual survival in this population. The propensity of banded pintails to return to our capture site (fidelity rate) varied between sexes and was positively correlated with water conditions in prairie Canada. Our estimates of fidelity rates varied from 77.4% to 87.2% for males and 89.8% to 94.3% for females. Our fidelity estimates suggest that some level of subpopulation structuring may exist for northern pintails. Additionally, our estimates of fidelity support previous observations of northern pintails overflying poor wetland habitat conditions on the Canadian prairies.

Journal of Wildlife Management