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9 results for “Eliurus”
Fig. 6 in A New Species of the Eliurus majori Complex (Rodentia: Muroidea: Nesomyidae) from South-central Madagascar, with Remarks on Emergent Species Groupings in the Genus Eliurus
Fig. 6. Phenogram produced from clustering (UPGMA) of Mahalanobis' distances derived from discriminant function analysis of 13 OTUs representing four species of Eliurus (see fig. 5).
Fig. 5 in A New Species of the Eliurus majori Complex (Rodentia: Muroidea: Nesomyidae) from South-central Madagascar, with Remarks on Emergent Species Groupings in the Genus Eliurus
Fig. 5. Results of discriminant function analysis performed on 18 log-transformed craniodental variables, as measured on 130 specimens representing 13 OTUs of Eliurus (see Materials and Methods). Top, projection of individual scores onto the first and second canonical variates extracted. Bottom, projection of
Fig. 4 in A New Species of the Eliurus majori Complex (Rodentia: Muroidea: Nesomyidae) from South-central Madagascar, with Remarks on Emergent Species Groupings in the Genus Eliurus
Fig. 4. Scatter plot of length of the upper molar row (LM1-3) versus greatest length of skull (ONL) for intact specimens of E. antsingy, E. danieli, E. majori, and E. penicillatus. Note that examples of the latter three species possess longer toothrows in relation to cranial size compared with those of E. antsingy.
Fig. 3 in A New Species of the Eliurus majori Complex (Rodentia: Muroidea: Nesomyidae) from South-central Madagascar, with Remarks on Emergent Species Groupings in the Genus Eliurus
Fig. 3. Lateral view (ca. 1.75X) of adult crania of species composing the Eliurus majori species group as recognized herein (same specimens as depicted in fig. 2): top, E. danieli new species; middle, E. majori; and bottom, E. penicillatus.
Fig. 1 in A New Species of the Eliurus majori Complex (Rodentia: Muroidea: Nesomyidae) from South-central Madagascar, with Remarks on Emergent Species Groupings in the Genus Eliurus
Fig. 1. Photograph of live Eliurus danieli (FMNH 175933), a young adult male from Andranohavo (Canyon des Rats) in the PN de l'Isalo. The new species is characterized by a bright white caudal tuft that is accentuated by the concentration of intensely black hairs along the middle portion of the tail. Photograph taken by Harald Schütz.
Fig. 2 in A New Species of the Eliurus majori Complex (Rodentia: Muroidea: Nesomyidae) from South-central Madagascar, with Remarks on Emergent Species Groupings in the Genus Eliurus
Fig. 2. Dorsal (upper row) and ventral (lower row) views (ca. 1.75X) of adult crania of species composing the Eliurus majori species group as recognized herein (see Discussion): left pair, E. penicillatus Thomas (USNM 49672; Fianarantsoa Province, Ampitambe, ca. 900 m; ONL 5 35.6 mm); middle pair, E. majori Thomas (FMNH 151663; Fianarantsoa Province, PN d'Andringitra, 40 km S Ambalavao, along Volotsangana River, 1210 m; ONL 5 38.1 mm); and right pair, E. danieli new species (FMNH 175934, type specimen; Fianarantsoa Province, Parc National de l'Isalo, 28 km SE Berenty-Betsileo, along Sahanafa River near foot of Bevato Mountain, 650 m; ONL 5 40.6 mm).
Data from: Latitude drives diversification in Madagascar's endemic dry forest rodent, Eliurus myoxinus (sub-family Nesomyinae)
Numerous hypotheses have been proposed for the historical processes governing the rich endemism of Madagascar's biodiversity. The 'watershed model' suggests that drier climates in the recent geological past have resulted in the contraction of forests around major watersheds, thereby defining areas of endemism. We test whether this hypothesis explains phylogeographical patterns in a dry forest-dependent rodent, Eliurus myoxinus, an endemic species widely distributed through western Madagascar. We sequenced the mitochondrial cytochrome b locus and nuclear introns of the β-fibrinogen and the growth hormone receptor genes for E. myoxinus. Using a parametric bootstrapping approach, we tested whether the mitochondrial gene tree data fit expectations of local differentiation given the watershed model. We additionally estimated population differentiation and historical demographic parameters, and reconstructed the spatial history of E. myoxinus to highlight spatial and temporal patterns of differentiation. The data do not support the watershed model as a clear explanation for the genetic patterns of diversity within extant E. myoxinus populations. We find striking patterns of latitudinal genetic structure within western Madagascar, and indicate possible roles for environmental and ecological gradients along this axis in generating phylogeographical diversity.
On following pages: 5. Carleton's Tufted-tail Rat (Eliurus carletoni); 6. Daniel's Tufted-tail Rat (Eliurus daniel); 7. Ellerman's Tufted-tail Rat (Eliurus ellermani); 8. Grandidier's Tufted-tail Rat (Eliurus grandidieri); 9. Major's Tufted-tail Rat (Eliurus majori); 10. Lesser Tufted-tail Rat (Eliurus minon; 11. Milne-Edwards's Tufted-tail Rat (Eliurus myoxinus); 12. White-tailed Tufted-tail Rat (Eliurus penicillatus); 13. Petters Tufted-tail Rat (Eliurus petteri); 14. Tanala Tuftedtail Rat (Eliurus tanala); 15. Webb's Tufted-tail Rat (Eliurus webbi); 16. Anjozorobe Naked-tail Forest Mouse (Voalavo antsahabensis); 17. Northern Naked-tail Forest Mouse (Voalavo gymnocaudus); 18. Bastard's Big-footed Mouse (Macrotarsomys bastard); 19. Ankarafantsika Big-footed Mouse (Macrotarsomys ingens); 20. Petter's Big-footed Mouse (Macrotarsomys petteri); 21. Koopman's Forest Mouse (Monticolomys koopmani); 22. Giant Jumping Rat (Hypogeomys antimena); 23. Small Short-tailed Rat (Brachyuromys betsileoensis); 24. Large Short-tailed Rat (Brachyuromys ramirohitra); 25. Audebert's Forest Rat (Nesomys audeberti); 26. Lamberton's Forest Rat (Nesomys lambertoni); 27. Red Forest Rat (Nesomys rufus); 28. Delany's Swamp Mouse (Delanymys brooksi); 29. African White-tailed Rat (Mystromys albicaudatus); 30. Shortridge''s Pygmy Rock Mouse (Petromyscus shortridgei): 31. Short-eared Pygmy Rock Mouse (Petromyscus monticularis); 32. Barbour's Pygmy Rock Mouse (Petromyscus barbouri); 33. Common Pygmy Rock Mouse (Petromyscus collinus). in Nesomyidae
On following pages: 5. Carleton's Tufted-tail Rat (Eliurus carletoni); 6. Daniel's Tufted-tail Rat (Eliurus daniel); 7. Ellerman's Tufted-tail Rat (Eliurus ellermani); 8. Grandidier's Tufted-tail Rat (Eliurus grandidieri); 9. Major's Tufted-tail Rat (Eliurus majori); 10. Lesser Tufted-tail Rat (Eliurus minon; 11. Milne-Edwards's Tufted-tail Rat (Eliurus myoxinus); 12. White-tailed Tufted-tail Rat (Eliurus penicillatus); 13. Petters Tufted-tail Rat (Eliurus petteri); 14. Tanala Tuftedtail Rat (Eliurus tanala); 15. Webb's Tufted-tail Rat (Eliurus webbi); 16. Anjozorobe Naked-tail Forest Mouse (Voalavo antsahabensis); 17. Northern Naked-tail Forest Mouse (Voalavo gymnocaudus); 18. Bastard's Big-footed Mouse (Macrotarsomys bastard); 19. Ankarafantsika Big-footed Mouse (Macrotarsomys ingens); 20. Petter's Big-footed Mouse (Macrotarsomys petteri); 21. Koopman's Forest Mouse (Monticolomys koopmani); 22. Giant Jumping Rat (Hypogeomys antimena); 23. Small Short-tailed Rat (Brachyuromys betsileoensis); 24. Large Short-tailed Rat (Brachyuromys ramirohitra); 25. Audebert's Forest Rat (Nesomys audeberti); 26. Lamberton's Forest Rat (Nesomys lambertoni); 27. Red Forest Rat (Nesomys rufus); 28. Delany's Swamp Mouse (Delanymys brooksi); 29. African White-tailed Rat (Mystromys albicaudatus); 30. Shortridge''s Pygmy Rock Mouse (Petromyscus shortridgei): 31. Short-eared Pygmy Rock Mouse (Petromyscus monticularis); 32. Barbour's Pygmy Rock Mouse (Petromyscus barbouri); 33. Common Pygmy Rock Mouse (Petromyscus collinus).
Data from: Latitude drives diversification in Madagascar’s endemic dry forest rodent, Eliurus myoxinus (sub-family Nesomyinae)
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