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18 results for “dormice”
FIG. 12 in They are all over the place! The exceptional high biodiversity of dormice in the Early Miocene of the Ribesalbes-Alcora Basin (Spain)
FIG. 12. — Distribution chart of the glirids listed in this paper, appears the sites well sampled and less sampled (not sufficiently sampled for the number of specimens to be statistically significant enough to accept or reject the presence of a taxon, see details in Crespo et al. 2019a). The thick line represents the change of local biozone. Abbreviations: MCX, Mas dels Coixos; MTR, Mas de Torner; BC, Barranc de Campisano; FS, Foieta la Sarra; MAB, Mas d'Antolino B; CBR, Corral de Brisca.
FIG. 9 in They are all over the place! The exceptional high biodiversity of dormice in the Early Miocene of the Ribesalbes-Alcora Basin (Spain)
FIG. 9. — Gliridae from the Ribesalbes-Alcora Basin. Simplomys julii: A, left d4 (BC1-119); B, right p4 (MAB3-383); C, left p4 (MAB5-819); D, right p4 (MAB5- 132); E, left m1 (MAB5-601); F, right m1 (MAB5-598); G, left m1 (MAB3-437); H, left m2 (MAB5-248); I, right m2 (MAB5-15); J, right m2 (FS1-43); K, right m2 (BC1-132); L, left m3 (MAB5-619); M, left m3 (MAB3-489); N, right m3 (BC1-9); O, right D4 (MAB5-552); P, right P4 (MAB5-549); Q, left P4 (MAB5-548); R, left P4 (MAB3-250); S, left P4 (BC1-87); T, left M1 (MAB5-275); U, left M1 (MAB5-274); V, right M1 (MAB5-234); W, left M1 (MAB3-334); X, right M2 (MAB5-253); Y, right M2 (MAB5-235); Z, left M2 (MAB3-333); AA, right M2 (BC1-101); AB, left M3 (MAB5-858); AC, right M3 (MAB5-583); AD, right M3 (MAB5-579); AE, left M3 (MAB3-491). Scale bar: 1 mm.
FIG. 3 in They are all over the place! The exceptional high biodiversity of dormice in the Early Miocene of the Ribesalbes-Alcora Basin (Spain)
FIG. 3. — Gliridae from the Ribesalbes-Alcora Basin. Microdyromys legidensis: A, right d4 (MAB3-392); B, left p4 (MAB5-838); C, right p4 (MAB5-594); D, left p4 (MAB3-386); E, right m1 (MAB3-413); F, right m1 (MAB5-417); G, left m1 (MAB3-428); H, right m1 (MAB5-847); I, left m2 (MAB3-412); J, right m2 (MAB3-416); K, left m2 (MAB3-466); L, right m2 (MAB5-245); M, right m3 (MAB5-855); N, left m3 (MAB3-486); O, right P4 (MAB5-813); P, right P4 (MAB5-813); Q, left P4 (MAB5- 126); R, left P4 (MAB3-264); S, left M1 (MAB5-278); T, right M1 (MAB5-563); U, left M1 (MAB3-309); V, left M1 (MAB3-315); W, left M2 (MAB3-413); X, left M2 (MAB3-314); Y, right M2 (MAB5-279); Z, left M2 (CBR0B-29); AA, left M3 (MAB3-355); AB, left M3 (MAB3-357); AC, left M3 (MAB5-581); AD, right M3 (MAB5-829). Microdyromys koenigswaldi: AE, right p4 (FS1-41); AF, left m1 (FS1-46); AG, right M1 (BC1-130); AH, left M1 (FS1-37); AI, right M3 (BC1-10). Scale bar: 1 mm.
FIG. 4 in They are all over the place! The exceptional high biodiversity of dormice in the Early Miocene of the Ribesalbes-Alcora Basin (Spain)
FIG. 4. — Gliridae from the Ribesalbes-Alcora Basin. Microdyromys aff. monspeliensis: A, right d4 (MAB0B-24); B, right p4 (MAB3-391); C, left m1 (MAB5-848); D, right m1 (MAB5-614); E, right m1 (MAB3-424); F, left m2 (MAB3-426); G, right m2 (MAB5-613); H, right m2 (BC1-126); I, left m3 (MAB5-857); J, left P4 (MAB5- 848); K, left M1 (MAB3-310); L, right M1 (MAB3-316); M, left M1 (MAB5-281); N, left M1 (MAB11-67); O, right M2 (MAB5-573); P, right M2 (MAB5-118); Q, left M2 (MAB3-313); R, right M3 (MAB5-584); S, left M3 (CBR0G-1); T, left M3 (MAB3-361). Prodryomys aff. satus: U, right m1 (MAB5-240); V, left m2 (MAB5-271); W, right M2 (MAB5-14); X, right M3 (MAB3-372). Prodryomys aff. remmerti: Y, left m3 (MAB3-473); Z, left P4 (MAB3-265); AA, right M1 (MAB3-332); AB, right M1 (MAB5-285); AC, left M2 (MAB3-349); AD, right M3 (MAB5-125); AE, right M3 (MAB5-125). Scale bar: 1 mm.
FIG. 1 in They are all over the place! The exceptional high biodiversity of dormice in the Early Miocene of the Ribesalbes-Alcora Basin (Spain)
FIG. 1. — Geographic and geological setting of the Ribesalbes-Alcora Basin, showing the location of the outcrops of the Campisano Ravine. Modified from Crespo et al. (2018; 2019a).
FIG. 2 in They are all over the place! The exceptional high biodiversity of dormice in the Early Miocene of the Ribesalbes-Alcora Basin (Spain)
FIG. 2. — Terminology of the glirids teeth modified from Freudenthal (2004) and García-Paredes et al. (2009).
FIG. 6 in They are all over the place! The exceptional high biodiversity of dormice in the Early Miocene of the Ribesalbes-Alcora Basin (Spain)
FIG. 6. — Gliridae from the Ribesalbes-Alcora Basin. Peridyromys murinus (continued): A, left D4 (MTR2-108); B, right D4 (MTR2-107); C, right D4 (MTR2-105); D, right D4 (MAB5-553); E, right D4 (BC1-14); F, left P4 (MTR2-103); G, left P4 (MTR2-99); H, right P4 (MTR2-10); I, right P4 (MAB5-811); J, right P4 (MAB3-252); K, right P4 (BC1-83); L, right maxilla M1+M2 (MCX3-100); M, right M1/M2 (MTR2-123); N, left M1/M2 (MTR2-121); O, left M1/M2 (MTR2-114); P, right M1/M2 (MTR2-113); Q, right M1/M2 (MTR2-110); R, left M1/M2 (MTR2-13); S, left M1/M2 (MTR2-12); T, left M1/M2 (MCX7-5); U, left M1/M2 (MAB5-558); V, right M1/M2 (MAB5-254); W, right M1/M2 (MAB3-326); X, right M3 (MAB3-356); Y, right M3 (MAB3-358); Z, left M3 (MAB11-70). Peridyromys darocensis: AA, left p4 (MAB11- 73); AB, right m1 (MAB11-76); AC, right m2 (MAB11-77); AD, right m3 (MAB11-82); AE, left M1/M2 (MAB5-270); AF, right M3 (MAB11-68). Scale bar: 1 mm.
FIG. 8 in They are all over the place! The exceptional high biodiversity of dormice in the Early Miocene of the Ribesalbes-Alcora Basin (Spain)
FIG. 8. — Gliridae from the Ribesalbes-Alcora Basin. Simplomys simplicidens: A, right d4 (MAB3-247); B, right p4 (MAB3-375); C, left p4 (MAB3-377); D, left p4 (MAB5-840); E, left m1 (MAB3-439); F, right m1 (MAB3-440); G, left m1 (MAB5-244); H, right m1 (MCX3-6); I, right m2 (BC1-6); J, left m2 (BC1-128); K, right m2 (MAB5-607); L, right m2 (MCX3-5); M, right m3 (MAB5-617); N, right m3 (MAB5-262); O, right m3 (MAB3-469); P, left m3 (MCX3-109); Q, right D4 (MAB11-56); R, right P4 (MAB3-254); S, right P4 (MAB3-257); T, left P4 (MAB5-287); U, left P4 (MTR2-102); V, left M1 (BC1-108); W, right M1 (BC1-110); X, right M1 (MAB5- 567); Y, right M1 (MTR2-128); Z, right M2 (MTR2-43); AA, left M2 (MCX3-1); AB, left M2 (MAB11-59); AC, right M2 (MAB5-269); AD, right M3 (MCX3-103); AE, right M3 (BC1-141); AF, right M3 (MAB0B-22); AG, right M3 (MAB5-578); AH, left M3 (MAB11-72). Scale bar: 1 mm.
FIG. 7 in They are all over the place! The exceptional high biodiversity of dormice in the Early Miocene of the Ribesalbes-Alcora Basin (Spain)
FIG. 7. — Gliridae from the Ribesalbes-Alcora Basin. Pseudodryomys ibericus: A, left d4 (MAB5-839); B, right d4 (MAB8-12); C, right p4 (MAB3-381); D, right p4 (MAB3A-4); E, right p4 (BC1-143); F, right m1 (MAB5-600); G, left m1 (MAB3-456); H, left m1 (MAB11-75); I, right m2 (MAB3-449); J, left m2 (MAB3A-2); K, right m3 (MAB3-472); L, right m3 (MTR2-148); M, left D4 (MAB3-259); N, left D4 (BC1-86); O, left D4 (CBR0G-2); P, right D4 (CBR0C-3); Q, left P4 (MAB3-258); R, right P4 (MAB5-124); S, left P4 (MAB0B-21); T, right M1 (MAB3-286); U, left M1 (MAB3-297); V, right M1 (MTR2-127); W, left M2 (MAB3-291); X, right M2 (MAB3-289); Y, right M2 (MAB0B-18); Z, right M2 (MCX1-4); AA, left M3 (MAB3-371); AB, right M3 (MAB5-861); AC, left M3 (BC1-111). Scale bar: 1 mm.
FIG. 11 in They are all over the place! The exceptional high biodiversity of dormice in the Early Miocene of the Ribesalbes-Alcora Basin (Spain)
FIG. 11. — Gliridae from the Ribesalbes-Alcora Basin. Glirudinus modestus: A, left d4 (MAB3-385); B, left p4 (MAB5-625); C, left p4 (MAB5-842); D, left p4 (MA- B11B-3); E, right m1 (MAB5-850); F, left m1 (MAB5-260); G, left m1 (MAB3-443); H, right m2 (MAB5-845); I, right m2 (MAB5-851); J, left m2 (MAB3-409); K, left m2 (MAB11-84); L, right m3 (MAB3-475); M, left m3 (MAB3-476); N, right m3 (MAB5-852); O, right P4 (MAB5-587); P, left P4 (MAB5-815); Q, right M1 (MAB5- 821); R, right M1 (MAB5-820); S, right M1 (MAB5-562); T, left M1 (MAB3-280); U, right M2 (MAB3-278); V, left M2 (MAB5-112); W, right M2 (MAB11-64); X, right M3 (MAB5-589); Y, left M3 (MAB5-588); Z, left M3 (MAB3-365). Myoglis cf. antecedens: AA, right P4 (MAB3-474); AB, right M3 (MAB3-367). Scale bar: 1 mm.
FIG. 10 in They are all over the place! The exceptional high biodiversity of dormice in the Early Miocene of the Ribesalbes-Alcora Basin (Spain)
FIG. 10. — Gliridae from the Ribesalbes-Alcora Basin. Simplomys meulenorum: A, right p4 (MAB3-389); B, left p4 (MAB11-10); C, left m2 (MAB3-450); D, left m3 (MAB5-860); E, left p4 (MAB3-269); F, right p4 (MAB3-270); G, right M1 (MAB3-298); H, right M1 (MAB3-299); I, left M1 (MAB3-300); J, left M2 (MAB3-302); K, left M2 (MAB3-287); L, left M2 (BC1-97). Armantomys aragonensis: M, left m1 (CBR0B-36); N, right m2 (CBR0B-37). Glirudinus undosus: O, left p4 (BC1-115); P, left m1 (MAB3-397); Q, right m1 (MAB3-400); R, right m1 (MAB3-403); S, left m1 (MAB5-20); T, rigth m2 (MAB3-395); U, left m2 (MAB3-396); V, right m3 (MAB3- 482); W, right M3 (MAB3-484); X, right P4 (MAB3-262); Y, left P4 (MAB3-236); Z, left P4 (MAB5-128); AA, left M1 (MAB3-272); AB, right M1 (MAB3-292); AC, right M1 (MAB5-109); AD, left M2 (MAB3-274); AE, left M3 (MAB3-366); AF, right M3 (MAB3-368). Scale bar: 1 mm.
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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Data from: Edible dormice (Glis glis) avoid areas with a high density of their preferred food plant - the European beech
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FIG. 5 in They are all over the place! The exceptional high biodiversity of dormice in the Early Miocene of the Ribesalbes-Alcora Basin (Spain)
FIG. 5. — Gliridae from the Ribesalbes-Alcora Basin. Bransatoglis cf. infralactorensis: A, right p4 (MAB3-382); B, right m1 (MAB3-399); C, right m1 (MAB11-78); D, left m2 (MAB5-258); E, right m2 (MAB0A-75); F, left m3 (MAB0A-74); G, left M3 (MAB3-295). Peridyromys murinus: H, right d4 (MAB0C-1); I, right p4 (BC1- 15); J, right p4 (BC1-113); K, right p4 (MAB3-380); L, left p4 (MAB13-2); M, right p4 (MTR2-130); N, right m1 (MTR2-133); O, left m1 (MTR2-132); P, right m1 (MTR2-131); Q, left m1 (MCX7-3); R, left m1 (MAB5-608); S, left m1 (MAB3-418); T, left m2 (MTR2-141); U, right m2 (MTR2-139); V, left m2 (MTR2-15); W, right m2 (MAB11-79); X, right m2 (FS1-44); Y, right m2 (BC1-120); Z, left m3 (MTR2-147); AA, right m3 (MTR2-146); AB, left m3 (MTR2-145); AC, right m3 (MAB3-468); AD, left m3 (MAB5-856); AE, right m3 (BC1-140). Scale bar: 1 mm.
Current nest box designs may not be optimal for the larger forest dormice; pre-hibernation increase in body mass might lead to sampling bias in ecological data
<p>Biologists commonly use nest boxes to study small arboreal mammals, including forest dormouse (Dryomys nitedula). Hibernating dormouse species often experience pronounced seasonal variations in body mass, which might lead to sampling biases if it is not taken into account when designing nest boxes. In our study of forest dormouse, we noticed that the entrance hole of nest boxes had been gnawed on. We hypothesized that this behavior was exhibited by individual dormice who had higher body mass and, therefore, were unable to pass through the entrance holes. To test our hypothesis, we categorized individual dormice present inside nest boxes based on their body mass; then compared the seasonal body mass dynamics with the timing of the gnawing behavior. We also compared nest box occupancy by forest dormouse before and after the gnawing behavior. Interestingly, we found that the gnawing behavior was displayed exclusively when part of the dormouse population increased considerably in body mass, which supports our hypothesis. Additionally, nest box occupancy decreased significantly from 20% before to 4.6% after the gnawing behavior. We suggest that researchers use nest boxes with entrance holes larger than 4 cm in future studies of forest dormouse to prevent the possible exclusion of the conspecifics that have higher body mass before hibernation. This type of sampling bias can probably happen in studies of other species, such as fat dormouse, that similarly show pronounced seasonal variations in body mass. We recommend that biologists consider the seasonal body mass dynamics of the target species when designing nest boxes to minimize bias in ecological data and improve management actions.</p>
Current nest box designs may not be optimal for the larger forest dormice; pre-hibernation increase in body mass might lead to sampling bias in ecological data
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