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11 results for “Muscardinus avellanarius”
Figure 1 in The importance of shape analysis of the first upper molar in the separation of two subspecies of the Hazel dormouse (Muscardinus avellanarius (Linnaeus, 1758)) in Northern Anatolia
Figure 1. Worldwide distribution of Muscardinus avellanarius (a) and trapped localities in Northern Anatolia, Turkey (b) [Number of specimens: in the West; Bolu = 23, Bursa = 3, Düzce = 6, and in the East; Giresun = 4, Ordu = 6, Trabzon = 14].
Figure 3 in The importance of shape analysis of the first upper molar in the separation of two subspecies of the Hazel dormouse (Muscardinus avellanarius (Linnaeus, 1758)) in Northern Anatolia
Figure 3. Harmonic order for the left first upper molar of M. avellanarius.
Figure 4 in The importance of shape analysis of the first upper molar in the separation of two subspecies of the Hazel dormouse (Muscardinus avellanarius (Linnaeus, 1758)) in Northern Anatolia
Figure 4. Positions of nine landmarks for the left first upper molar (Definitions are in the text).
Figure 6 in The importance of shape analysis of the first upper molar in the separation of two subspecies of the Hazel dormouse (Muscardinus avellanarius (Linnaeus, 1758)) in Northern Anatolia
Figure 6. Canonical variate analysis of M. avellanarius on the M1 for landmark analysis.
Figure 2 in The importance of shape analysis of the first upper molar in the separation of two subspecies of the Hazel dormouse (Muscardinus avellanarius (Linnaeus, 1758)) in Northern Anatolia
Figure 2. Occlusal surface of the left first upper molar and start position of digitisations.
Figure 5 in The importance of shape analysis of the first upper molar in the separation of two subspecies of the Hazel dormouse (Muscardinus avellanarius (Linnaeus, 1758)) in Northern Anatolia
Figure 5. Canonical variate analysis of M. avellanarius on the M1 for outline analysis.
Data for: Nest material preferences in wild hazel dormice Muscardinus avellanarius: Testing predictions from optimal foraging theory
<p class="MsoNormal">Obtaining nesting material presents an optimal foraging problem, collection of materials incurs a cost in terms of risk of predation and energy spent, and individuals must balance these costs with the benefits of using that material in the nest. The hazel dormouse, <em>Muscardinus avellanarius</em> is an endangered British mammal in which both sexes build nests. However, whether material used in their construction follows the predictions of optimal foraging theory is unknown. Here, we analyse the use of nesting materials in forty two breeding nests from six locations in Southwest England. Nests were characterised in terms of which plants were used, the relative amount of each plant, and how far away the nearest source was. We find that dormice exhibit a preference for plants closer to the nest, but that the distance they are prepared to travel depends on the plant species. Dormice travelled further to collect honeysuckle <em>Lonicera periclymenum</em>, oak <em>Quercus robur</em>, and beech <em>Fagus sylvatica</em> than any other plants. Distance did not affect the relative amount used, although the proportion of honeysuckle in nests was highest, and more effort was expended collecting honeysuckle, beech, bramble <em>Rubus fruticosus</em> and oak compared to other plants. Our results suggest that not all aspects of optimal foraging theory apply to nest material collection. However, optimal foraging theory is a useful model to examine nest material collection, providing testable predictions. As found previously honeysuckle is important as a nesting material, and should be taken account when assessing suitability of sites for dormice.</p>
Data from: Machine learning identification of microhabitat features associated with occupancy of artificial nestboxes by hazel dormice (Muscardinus avellanarius) in a UK woodland site
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Data for: Nest material preferences in wild hazel dormice Muscardinus avellanarius: Testing predictions from optimal foraging theory
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On following pages: 17. Fat Dormouse (Glis glis); 18. Hazel Dormouse (Muscardinus avellanarius); 19. Roach''s Mouse-tailed Dormouse (Myomimus roachi); 20. Setzer's Mouse-tailed Dormouse (Myomimus setzeri); 21. Ognev's Mouse-tailed Dormouse (Myomimus personatus); 22. Desert Dormouse (Selevinia betpakdalaensis); 23. Sichuan Dormouse (Chaetocauda sichuanensis); 24. Eurasian Forest Dormouse (Dryomys nitedula); 25. Woolly Forest Dormouse (Dryomys lanigen; 26. Niethammer's Forest Dormouse (Dryomys niethammeri); 27. Black-tailed Garden Dormouse (Eliomys melanurus); 28. European Garden Dormouse (Eliomys quercinus); 29. Maghreb Garden Dormouse (Eliomys munbyanus). in Gliridae
On following pages: 17. Fat Dormouse (Glis glis); 18. Hazel Dormouse (Muscardinus avellanarius); 19. Roach''s Mouse-tailed Dormouse (Myomimus roachi); 20. Setzer's Mouse-tailed Dormouse (Myomimus setzeri); 21. Ognev's Mouse-tailed Dormouse (Myomimus personatus); 22. Desert Dormouse (Selevinia betpakdalaensis); 23. Sichuan Dormouse (Chaetocauda sichuanensis); 24. Eurasian Forest Dormouse (Dryomys nitedula); 25. Woolly Forest Dormouse (Dryomys lanigen; 26. Niethammer's Forest Dormouse (Dryomys niethammeri); 27. Black-tailed Garden Dormouse (Eliomys melanurus); 28. European Garden Dormouse (Eliomys quercinus); 29. Maghreb Garden Dormouse (Eliomys munbyanus).
Effects of food availability on the trophic niche of the hazel dormouse Muscardinus avellanarius
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