67 research outputs found

    Diving angle of great cormorants

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    Seabirds can maximize the relative time spent at depths where prey occur by minimizing the commuting time taken to reach these depths. One way to achieve this goal is to modify dive angle, but there are few measures of dive-angle in free-foraging seabirds. In 2003, we monitored simultaneously the swimming speeds and diving depths of great cormorants (Phalacrocorax carbo) foraging off the Greenland coast, and used these data to reconstruct their descent angle. Both males and females dived on average 12 m. We suggest that birds are able to reduce their descent time for dives beyond this depth by performing pre-dive leaps that allow them to use the momentum of the fall to descend almost vertically and at great speeds. Such pre-dive leaps in shallower dives would be unsuitable because of the proximity of the seabed and the risk of startling prey. Finally, in contrast with deeper divers, descent angles were not steeper when undulations were observed in the depth profile of the previous dive, probably because birds feed on dispersed prey

    Low-density open-cell foams in the NiTi system

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    It is shown that open-cell metallic foams having very low density, and that display martensite transformations required for shape memory and superelastic behavior, can be fabricated using a powder-metallurgy technique. Results are presented on experiments in which a polymeric precursor foam was coated with an equiatomic NiTi powder slurry and subsequently sintered to yield foams with relative densities as low as 0.039. Although contaminated with interstitial impurities, they displayed unambiguous calorimetric signature of the B2→B19â€ČB2→B19â€Č transformation. The results are of considerable significance to potential applications requiring ultralightweight structures with the unusual dissipative and strain-recovery properties of NiTi shape-memory materials. © 2003 American Institute of Physics.Peer Reviewedhttp://deepblue.lib.umich.edu/bitstream/2027.42/71336/2/APPLAB-82-16-2727-1.pd

    Three-dimensional space utilisation in a marine predator

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    Diving seabirds should evolve a variety of foraging characteristics which enable them to minimize energy expenditure and to maximize net energy gain while searching for prey underwater. In order to assess the related ecological adaptations in a marine predator, we studied the at-sea distribution and the diving behaviour of 23 cormorants Phalacrocorax carbo (Linnaeus) breeding at the Chausey Islands (France) using VHF-telemetry and data loggers recording hydrostatic pressure. Birds foraged within an area of approximately 1131 km2 situated north-east of the breeding colony. This zone represents only 25% of the maximal potentially available area that the birds may utilize considering their maximum foraging range of 35 km. Individual birds remained within restricted individual foraging areas (on average 18 and 10% of the total utilized area in 1994 and 1995, respectively) throughout the study period. Moreover, the cormorants studied conducted an average of 42 dives per foraging trip, lasting for an average of 40 s (maximum 152 s), and reached an average maximum dive depth of 6.1 m (maximum 32 m) with median descent and ascent angles calculated to be 18.7° and 20.3°, respectively. Overall, 64% of all dives were U-shaped dives and 36% V-shaped dives. We use these results to demonstrate how both specialization and opportunism may support the remarkably high foraging efficiency of this marine predator

    A tropical bird in the Artic (The Cormorant paradox)

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    Seabirds, like all marine endotherms, have to compensate for the extensive cooling effect of water when diving. Alone among them, cormorants (Phalacrocoracidae) have a wettable plumage and are predicted to require disproportionately large amounts of food to balance heat losses. These piscivorous birds are thus thought to have a detrimental impact on fish stocks. However, we show here that even in great cormorants from Greenland, which dive in water at 3 to 7°C, daily food intake is lower than for well-insulated European seabirds. Despite their wettable plumage, cormorants thus appear to manage their energy budgets in a remarkably efficient way. Nevertheless, the specific foraging strategies which enable this performance make cormorants dependent on high prey density areas, a feature that should be taken into account by future management plans

    Projected distributions of Southern Ocean albatrosses, petrels and fisheries as a consequence of climatic change

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    Given the major ongoing influence of environmental change on the oceans, there is a need to understand and predict the future distributions of marine species in order to plan appropriate mitigation to conserve vulnerable species and ecosystems. In this study we use tracking data from seven large seabird species of the Southern Ocean (black‐browed albatross Thalassarche melanophris, grey‐headed albatross T. chrysostoma, northern giant petrel Macronectes halli, southern giant petrel M. giganteus, Tristan albatross Diomedea dabbenena, wandering albatross D. exulans and white‐chinned petrel Procellaria aequinoctialis, and on fishing effort in two types of fisheries (characterised by low or high‐bycatch rates), to model the associations with environmental variables (bathymetry, chlorophyll‐a concentration, sea surface temperature and wind speed) through ensemble species distribution models. We then projected these distributions according to four climate change scenarios built by the Intergovernmental Panel for Climate Change for 2050 and 2100. The resulting projections were consistent across scenarios, indicating that there is a strong likelihood of poleward shifts in distribution of seabirds, and several range contractions (resulting from a shift in the northern, but no change in the southern limit of the range in four species). Current trends for southerly shifts in fisheries distributions are also set to continue under these climate change scenarios at least until 2100; some of these may reflect habitat loss for target species that are already over‐fished. It is of particular concern that a shift in the distribution of several highly threatened seabird species would increase their overlap with fisheries where there is a high‐bycatch risk. Under such scenarios, the associated shifts in distribution of seabirds and increases in bycatch risk will require much‐improved fisheries management in these sensitive areas to minimise impacts on populations in decline
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