20,262 research outputs found
Differences in the trophic ecology of micronekton driven by diel vertical migration.
Many species of micronekton perform diel vertical migrations (DVMs), which ultimately contributes to carbon export to the deep sea. However, not all micronekton species perform DVM, and the nonmigrators, which are often understudied, have different energetic requirements that might be reflected in their trophic ecology. We analyze bulk tissue and whole animal stable nitrogen isotopic compositions (δ 15N values) of micronekton species collected seasonally between 0 and 1250 m depth to explore differences in the trophic ecology of vertically migrating and nonmigrating micronekton in the central North Pacific. Nonmigrating species exhibit depth-related increases in δ 15N values mirroring their main prey, zooplankton. Higher variance in δ 15N values of bathypelagic species points to the increasing reliance of deeper dwelling micronekton on microbially reworked, very small suspended particles. Migrators have higher δ 15N values than nonmigrators inhabiting the epipelagic zone, suggesting the consumption of material during the day at depth, not only at night when they migrate closer to the surface. Migrating species also appear to eat larger prey and exhibit a higher range of variation in δ 15N values seasonally than nonmigrators, likely because of their higher energy needs. The dependence on material at depth enriched in 15N relative to surface particles is higher in migratory fish that ascend only to the lower epipelagic zone. Our results confirm that stark differences in the food habits and dietary sources of micronekton species are driven by vertical migrations
The control of indirect effects of biomanipulation
Results from long-term investigations on biomanipulation show that indirect effects are at least as important as direct effects are for the stability of biomanipulation. Three types of indirect effects can be distinguished: (1) a change in quantity or quality of the resource base, (2) behavioural change of the prey, and (3) development of anti-predator traits. Although indirect effects of type (2), (e.g. a change in the pattern of vertical migration of zooplankton), and type (3), (e.g. development of helmets and neck teeth in Daphnia), are important mechanisms, the most essential indirect effects regarding biomanipulation belong to type (1). An example of the latter will be demonstrated: the complex of indirect effects of enhanced grazing by large herbivores on the phosphorus metabolism of the lake. It is concluded that control of the indirect effects is absolutely necessary to stabilize biomanipulation measures, but this is much more difficult than the control of direct effects and needs deeper insights into the structuring mechanisms of food webs. Proper management of fish stocks, in combination with the control of phosphorus load and/or the physical conditions, seems to be the most promising way of controlling the indirect effects of biomanipulation
Seasonal body mass changes in Eurasian Golden Plovers Pluvialis apricaria staging in the Netherlands: decline in late autumn mass peak correlates with increase in raptor numbers
Eurasian Golden Plovers Pluvialis apricaria staging in the Netherlands during the non-breeding season show strikingly constant seasonal changes in body mass with a first mass peak in late November and December and a second peak in late April and May. Despite huge sample sizes, variations in this pattern over successive years in the 1990s and among age classes were minuscule. However, in contrast to the body mass levels at other times of the year, there was a marked decline in the winter peak mass of Golden Plovers from the 1970s/early 1980s to 1989–2000. The decrease, by an average of 29 g, was about half the extra mass previously stored in autumn. This additional mass is known to consist of fat and may be interpreted as an energy store − insurance − for sudden cold spells when a negative energy balance forces the birds to move south and stay in front of the frostline. As the rate of the mass increase in September–October showed no change from the 1980s to the 1990s, changes in food availability are unlikely to explain the long-term mass decline. Also, there were no differences in two factors known to influence energy expenditure and feeding rate, air temperature and rainfall. The one striking environmental change relevant to plovers was the steep increase in the occurrence of raptors in the northern Netherlands in the 1980s, notably Peregrine Falcons Falco peregrinus and Goshawks Accipter gentilis. We argue that the halving of the winter mass peak over a decade is consistent with the hypothesis that under increased risk of predation, birds lower their body mass in order to reduce individual vulnerability, a reduction that may be traded off against an increased risk of starvation.
Trade-offs, condition dependence and stopover site selection by migrating sandpipers
Western sandpipers Calidris mauri on southward migration fly over the Gulf of Alaska to the Strait of Georgia, British Columbia, where they stop for a few days to replenish reserves before continuing. In the Strait, individuals captured on the extensive tidal mudflats of the Fraser estuary (∼25000 ha) are significantly heavier (2.71 g, or >10% of lean body mass) than those captured on the small (<100 ha) mudflat of nearby Sidney Island. Previous work has shown that the difference cannot be attributed to seasonal timing, size, age or gender effects, and here we compare predictions made by six hypotheses about a diverse set of data to explain why, partway through a migratory journey of ∼10000 km, birds have such different body masses at two stopover sites within 40 km of each other. The ‘trade-off’ hypothesis – that the large Fraser estuary offers safety from predators, but a lower fattening rate, while the small Sidney Island site is more dangerous, but offers a higher fattening rate – made six successful predictions, all of which were upheld by the data. All other hypotheses failed at least one prediction. We infer that calidrid sandpipers arriving in the Strait of Georgia with little fat remaining (and therefore low body mass) choose to take advantage of the high feeding rate at small sites like Sidney Island because they are less vulnerable to avian predators than are individuals with higher fat reserves, who instead elect to feed at large open sites like the Fraser estuary mudflats
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