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Ann Harding

Publications and source records attributed to Ann Harding.

4 recordsLinked to original sources

Flexibility in the parental effort of an Arctic-breeding seabird

Parental investment strategies are considered to represent a trade-off between the benefits of investment in current offspring and costs to future reproduction. Due to their high residual reproductive value, long-lived organisms are predicted to be more reluctant to increase parental effort. 2. We tested the hypothesis that breeding little auks (Alle alle) have a fixed level of reproductive investment, and thus reduce parental effort when costs associated with reproduction increase. 3. To test this hypothesis we experimentally increased the flight costs of breeding little auks via feather clipping. In 2005 we examined changes in the condition of manipulated parents, of the mates of manipulated parents, and of their chick as direct measures of change in parental resource allocation between self-maintenance and current reproduction. In 2007 we increased sample sizes to determine whether there was a physiological cost (elevated corticosterone, CORT) associated with the manipulation. 4. We found that: (i) clipped birds and their mates lost more body mass than controls, but there was no difference in mass loss between members of a pair; (ii) clipped birds had higher CORT levels than control birds; (iii) there were no inter-annual differences in body mass and CORT levels between clipped individuals and their mates at recapture, and (iv) chicks with a clipped parent had lower peak and fledging mass, and higher CORT levels than control chicks in both years. 5. Contrary to our hypothesis, the reduction in body mass of partners to clipped birds suggests that little auks can increase parental effort to some extent. Nonetheless, the lower fledging mass and higher CORT of chicks with a clipped parent indicates provisioning rates may not have been fully maintained. 6. As predicted by life-history theory, there may be a threshold to the additional reproductive costs breeders will accept, with parents prioritizing self-maintenance over increased provisioning effort when foraging costs become too high. ?? 2008 British Ecological Society.

Functional Ecology

Impacts of experimentally increased foraging effort on the family: offspring sex matters

We examined how short-term impacts of experimentally increased foraging effort by one parent reverberate around the family in a monomorphic seabird (little auk, Alle alle), and whether these effects depend on offspring sex. In many species, more effort is required to rear sons successfully than daughters. However, undernourishment may have stronger adverse consequences for male offspring, which could result in a lower fitness benefit of additional parental effort when rearing a son. We tested two alternative hypotheses concerning the responses of partners to handicapping parents via feather clipping: partners rearing a son are (1) more willing or able to compensate for the reduced contribution of their mate, or (2) less willing or able to compensate, compared to those rearing a daughter. Hypothesis 1 predicts that sons will be no more adversely affected than daughters, and the impact on parents will be greater when rearing a son. Hypothesis 2 predicts that sons will be more adversely affected than daughters, and parents raising a son less affected. Although experimental chicks of both sexes fledged in poorer condition than controls, sons attained higher mass and more rapid growth than daughters in both groups. Clipped parents lost a similar proportion of their initial mass regardless of chick sex, whereas partners of clipped birds lost more mass when rearing a son. These results support hypothesis 1: impacts of increased foraging effort by one parent were felt by offspring, regardless of their sex, and by the partners of manipulated birds, particularly when the offspring was male. ?? 2009 The Association for the Study of Animal Behaviour.

Animal Behaviour

Seabirds as indicators of marine food supplies: Cairns revisited

In his seminal paper about using seabirds as indicators of marine food supplies, Cairns (1987, Biol Oceanogr 5:261&ndash;271) predicted that (1) parameters of seabird biology and behavior would vary in curvilinear fashion with changes in food supply, (2) the threshold of prey density over which birds responded would be different for each parameter, and (3) different seabird species would respond differently to variation in food availability depending on foraging behavior and ability to adjust time budgets. We tested these predictions using data collected at colonies of common murre Uria aalge and black-legged kittiwake Rissa tridactyla in Cook Inlet, Alaska. (1) Of 22 seabird responses fitted with linear and non-linear functions, 16 responses exhibited significant curvilinear shapes, and Akaike&rsquo;s information criterion (AIC) analysis indicated that curvilinear functions provided the best-fitting model for 12 of those. (2) However, there were few differences among parameters in their threshold to prey density, presumably because most responses ultimately depend upon a single threshold for prey acquisition at sea. (3) There were similarities and some differences in how species responded to variability in prey density. Both murres and kittiwakes minimized variability (CV < 15%) in their own body condition and growth of chicks in the face of high annual variability (CV = 69%) in local prey density. Whereas kittiwake breeding success (CV = 63%, r 2 = 0.89) reflected prey variability, murre breeding success did not (CV = 29%, r 2 < 0.00). It appears that murres were able to buffer breeding success by reallocating discretionary &lsquo;loafing&rsquo; time to foraging effort in response (r 2 = 0.64) to declining prey density. Kittiwakes had little or no discretionary time, so fledging success was a more direct function of local prey density. Implications of these results for using &lsquo;seabirds as indicators&rsquo; are discussed.

Marine Ecology Progress Series