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1 on the population and distribution of Peleng tarsiers.
2 356) to process visual information as does a tarsier (87).
3             This new specimen indicates that tarsiers already possessed greatly enlarged orbits and a
4                        The placements of the tarsier and the tree shrew within and in relation to pri
5 rom the last common ancestor of haplorhines (tarsiers and anthropoids) to that of anthropoids (New Wo
6 tical to the corresponding anatomy in living tarsiers and differs substantially from that of early an
7                                              Tarsiers and extinct tarsier-like primates have played a
8  lemur species and only minor defects in two tarsiers and two nocturnal lemurs.
9                                              Tarsiers are phylogenetically located between the most b
10 ng been regarded as the nearest relatives of tarsiers, but a sister group relationship between anthro
11                                              Tarsier central cones had 2-microm-wide outer (OS) and i
12 d L/M cone systems are yet to be determined, tarsier cone proteins and distribution have some similar
13    This is comparable to the broad ranges of tarsier densities throughout Sulawesi and offshore islan
14 ptive shift that occurred at the base of the tarsier-eosimiid-anthropoid clade.
15 r group relationship between anthropoids and tarsiers has also been proposed.
16 anatomy, but until now, the fossil record of tarsiers has been limited to a single jaw and several is
17                 Because of the importance of tarsiers in so many primatological problems, there has b
18                         Tarsiers and extinct tarsier-like primates have played a central role in view
19                           We determined that tarsiers only occur on Peleng and Banggai Island.
20 ith our new data, we believe that the Peleng tarsier population should be classified as "Vulnerable".
21                 The phylogenetic position of tarsiers relative to anthropoids and Paleogene omomyids
22                              Only Macaca and tarsier retina contained cones labeled by antiserum to s
23                                           In tarsier retinal whole-mounts, peak cone density ranged f
24                                              Tarsier rod cell bodies were 6-12 deep, depending on ret
25 though the functional characteristics of the tarsier S and L/M cone systems are yet to be determined,
26 ar interest in questions about the origin of tarsier specializations and the biogeography of early ta
27 rtion within the nuclear genome, then reveal tarsier-specific, positive gene selection and posit popu
28                                   The Peleng tarsier (Tarsius pelengensis) is poorly known primate, w
29 here a new genome assembly of the Philippine tarsier (Tarsius syrichta), and provide extended analyse
30  the ferroportin from the primate Philippine tarsier (TsFpn) in the presence and absence of hepcidin
31                                       Peleng tarsiers were found in all elevations (0-937 m above sea
32                 The evolutionary position of tarsiers with respect to primates is still debated.