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6 results for “Diving depth”
Рис. 3. Фотографии Laternula elliptica, сделанные около cтанции «Прогресс», ВосточнаЯ Антарктида. L. elliptica на морском дне с медкими камнЯми или гравием, глубина 27 м (А); несколько сифональных отверстий L. elliptica над поверхностью мЯгких осадков вокруг голотурии Staurocucumis turqueti, глубина 27 м (В); раковина L. elliptica (длина около 110 мм) на снегу около майны сраЗу после иЗвлечениЯ иЗ воды (С); пустые раковины L. elliptica на морском дне, глубина 56 м (D); раковина L. elliptica (вид с дорсального краЯ) на мЯгких осадках с камнЯми, покрытыми иЗвестковыми водорослЯми, глубина 30 м (Е); пара сифональных отверстий L. elliptica на поверхности мЯгких осадков, глубина 27 м (F). Фотографии О. Савинкина (A, B, D–F) и В. Потина (С). Fig. 3. Photographs of Laternula elliptica taken near «Progress» Research Station (East Antarctica). Softshelled clam L. elliptica on sea bottom with small stowns or gravel, depth 27 m (A); several open siphons of L. elliptica above soft bottom sediments around holothurian Staurocucumis turqueti, depth 27 m (B); a shell of L. elliptica (length about 110 mm) on snow near a dive hole just after dragging out of water (C); empty shells of L. elliptica on seafloor, depth 56 m (D); a shell of Laternula elliptica (dorsal view) on soft deposits among stones, covering by Lithothamnion, depth 30 m (E); pair of siphonal opening of L. elliptica on surface of soft sediments, depth 27 m (F). Photographs are taken by O. Savinkin (A, B, D–F) and V. Potin (C). in Species of warm-water origin Laternula elliptica (King, 1832) (Mollusca: Bivalvia: Laternulidae), a widespread mollusk in recent Antarctica
Рис. 3. Фотографии Laternula elliptica, сделанные около cтанции «Прогресс», ВосточнаЯ Антарктида. L. elliptica на морском дне с медкими камнЯми или гравием, глубина 27 м (А); несколько сифональных отверстий L. elliptica над поверхностью мЯгких осадков вокруг голотурии Staurocucumis turqueti, глубина 27 м (В); раковина L. elliptica (длина около 110 мм) на снегу около майны сраЗу после иЗвлечениЯ иЗ воды (С); пустые раковины L. elliptica на морском дне, глубина 56 м (D); раковина L. elliptica (вид с дорсального краЯ) на мЯгких осадках с камнЯми, покрытыми иЗвестковыми водорослЯми, глубина 30 м (Е); пара сифональных отверстий L. elliptica на поверхности мЯгких осадков, глубина 27 м (F). Фотографии О. Савинкина (A, B, D–F) и В. Потина (С). Fig. 3. Photographs of Laternula elliptica taken near «Progress» Research Station (East Antarctica). Softshelled clam L. elliptica on sea bottom with small stowns or gravel, depth 27 m (A); several open siphons of L. elliptica above soft bottom sediments around holothurian Staurocucumis turqueti, depth 27 m (B); a shell of L. elliptica (length about 110 mm) on snow near a dive hole just after dragging out of water (C); empty shells of L. elliptica on seafloor, depth 56 m (D); a shell of Laternula elliptica (dorsal view) on soft deposits among stones, covering by Lithothamnion, depth 30 m (E); pair of siphonal opening of L. elliptica on surface of soft sediments, depth 27 m (F). Photographs are taken by O. Savinkin (A, B, D–F) and V. Potin (C).
Data for: Brain activity of diving seals reveals short sleep cycles at depth
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Data from: Olfaction at depth: cribriform plate size declines with dive depth and duration in aquatic arctoid carnivorans
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Data from: Depth dependent dive kinematics suggest cost-efficient foraging strategies by tiger sharks
Tiger sharks Galeocerdo cuvier are a keystone, top-order predator that are assumed to engage in cost-efficient movement and foraging patterns. To investigate the extent to which patterns of oscillatory diving by these animals conform to these patterns, we used a biologging approach to model their cost of transport. High-resolution biologging tags with tri-axial sensors were deployed on 21 tiger sharks at Ningaloo Reef for durations of 5-48 hours. Using overall dynamic body acceleration (ODBA) as a proxy for energy expenditure, we modelled the cost of transport of oscillatory movements of varying geometries in both horizontal and vertical planes for tiger sharks. The cost of horizontal transport was minimized by descending at the lowest possible angle and ascending at an angle of 5-14°, meaning that vertical oscillations conserved energy compared to swimming at a level depth. Reduction of vertical travel costs occurred at steeper angles. The absolute dive angles of tiger sharks increased between inshore and offshore zones, presumably to reduce the cost of transport while continuously hunting for prey in both benthic and surface habitats. Oscillatory movements of tiger sharks conform to strategies of cost-efficient foraging, and shallow inshore habitats appear to be an important habitat for both hunting prey and conserving energy while travelling.
Data from: Depth dependent dive kinematics suggest cost-efficient foraging strategies by tiger sharks
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Seabird species with no diving depth literature
<p>List of seabirds with no diving depth / foraging literature</p>
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