We compared prefledging growth, energy expenditure, and time budgets in the arctic-breeding red knot (Calidris canutus) to those in temperate shorebirds, to investigate how arctic chicks achieve a high growth rate despite energetic difficulties associated with precocial development in a cold climate. Growth rate of knot chicks was very high compared to other, mainly temperate, shorebirds of their size, but strongly correlated with weather-induced and seasonal variation in availability of invertebrate prey. Red knot chicks sought less parental brooding and foraged more at the same mass and temperature than chicks of three temperate shorebird species studied in The Netherlands. Fast growth and high muscular activity in the cold tundra environment led to high energy expenditure, as measured using doubly labelled water: total metabolised energy over the 18-day prefledging period was 89% above an allometric prediction, and among the highest values reported for birds. A comparative simulation model based on our observations and data for temperate shorebird chicks showed that several factors combine to enable red knots to meet these high energy requirements: (1) the greater cold-hardiness of red knot chicks increases time available for foraging; (2) their fast growth further shortens the period in which chicks depend on brooding; and (3) the 24-h daylight increases potential foraging time, though knots apparently did not make full use of this. These mechanisms buffer the loss of foraging time due to increased need for brooding at arctic temperatures, but not enough to satisfy the high energy requirements without invoking (4) a higher foraging intake rate as an explanation. Since surface-active arthropods were not more abundant in our arctic study site than in a temperate grassland, this may be due to easier detection or capture of prey in the tundra. The model also suggested that the cold-hardiness of red knot chicks is critical in allowing them sufficient feeding time during the first week of life. Chicks hatched just after the peak of prey abundance in mid-July, but their food requirements were maximal at older ages, when arthropods were already declining. Snow cover early in the season prevented a better temporal match between chick energy requirements and food availability, and this may enforce selection for rapid growth.
Birds on migration alternate between consuming fuel stores during flights and accumulating fuel stores during stopovers. The optimal timing and length of flights and stopovers for successful migration depend heavily on the extra metabolic power input (fuel use) required to carry the fuel stores during flight. The effect of large fuel loads on metabolic power input has never been empirically determined. We measured the total metabolic power input of a long-distance migrant, the red knot (Calidris canutus), flying for 6 to 10 h in a wind tunnel, using the doubly labelled water technique. Here we show that total metabolic power input increased with fuel load, but proportionally less than the predicted mechanical power output from the flight muscles. The most likely explanation is that the efficiency with which metabolic power input is converted into mechanical output by the flight muscles increases with fuel load. This will influence current models of bird flight and bird migration. It may also help to explain why some shorebirds, despite the high metabolic power input required to fly, routinely make nonstop flights of 4,000 km longer.
We estimated the consumption of juvenile salmonids (Oncorhynchus spp.) and other forage fishes by Caspian terns (Sterna caspia) nesting on Rice Island in the Columbia River estuary in 1997 and 1998 using a bioenergetics modeling approach. The study was prompted by concern that Caspian tern predation might be a substantial source of mortality to out-migrating juvenile salmonids from throughout the Columbia River basin, many populations of which are listed as threatened or endangered under the U.S. Endangered Species Act. The bioenergetics model used estimates of the energy requirements of the tern population and the proportion of tern energy requirements met by various prey types. The resulting estimate of the number of juvenile salmonids consumed by Rice Island Caspian terns was 8.1 million (5.910.4 million) in 1997 and 12.4 million (9.115.7 million) in 1998. Tern predation rates on juvenile salmonids were substantial, representing up to 15% of the juveniles to reach the estuary from some listed populations. Nevertheless, based on simple age-structured models of salmonid populations, it appears unlikely that management of Caspian tern predation alone would reverse salmonid declines. Management to reduce tern predation could, however, contribute to a comprehensive strategy to recover imperiled salmonid populations in the Columbia River basin.
The cost offeather production, Cf (kJ . [g dry feathers]-1), differs substantially between species. We studied the molt cost in one insectivorous songbird (bluethroat, Luscinia s. svecica) and one granivorous songbird (common redpoll, Carduelis f. flammea). We wanted to test whether diferences in diet, body mass (or basal metabolic rate, BMR), or the latitude of molt could explain interspecific differences. In each individual, the resting metabolism, as measured by indirect calorimetry, waspositively correlated with feather production rate. The cost of feather synthesis was estimated at 836 and 683 kJ. (g dry feathers)-1 in the bluethroats and redpolls, respectively. The efciency offeatherproduction was 2.6% and 3. 1%. It was concluded that neither diet nor latitudinal constraints alone could explain the differences found between species. The cost offeather production was significantly correlated with both body mass and mass-specific BMR, BMRm (kJ . g-. d-1), where BMRm currently showed the highest degree of explanation, although other factors that influence BMRm cannot be discounted. The Cf for a species with known BMRm may be estimated from the equation Cf = 270 BMRm. Species with a relatively high BMRfor their size also have a relatively high Cf The tight association of Cf and BMRm between species, and the low efciency values offeather synthesis, suggests that feather production costs include more than the costs for keratin synthesis: they mainly consist of costs of maintaining tissues necessary forfeather production.
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