2009
DOI: 10.1206/322.1
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Phylogenetic Relationships and Classification of Didelphid Marsupials, an Extant Radiation of New World Metatherian Mammals

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Cited by 311 publications
(518 citation statements)
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References 224 publications
(315 reference statements)
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“…Furthermore, our specimen can be identified as C. unduaviensis by the following combination of characters: tail length more than 111 mm (Table 2), condylobasal length more than 25.5 mm, maxillary too throw more than 10.0 mm, length of upper molar series (M1-M4) more than 5.5 mm; venter self-colored light yellowish buff. The characters and measurements of our specimen fell within the range of variation described for C. unduaviensis in the literature Gardner, 2007b;Voss & Jansa, 2009;Voss, com. pers.…”
Section: Richnesssupporting
confidence: 76%
“…Furthermore, our specimen can be identified as C. unduaviensis by the following combination of characters: tail length more than 111 mm (Table 2), condylobasal length more than 25.5 mm, maxillary too throw more than 10.0 mm, length of upper molar series (M1-M4) more than 5.5 mm; venter self-colored light yellowish buff. The characters and measurements of our specimen fell within the range of variation described for C. unduaviensis in the literature Gardner, 2007b;Voss & Jansa, 2009;Voss, com. pers.…”
Section: Richnesssupporting
confidence: 76%
“…There was no significant difference between bones found in the white-eared opossum skull when compared with those described for other mammals, as of porcupine (Yilmaz 1998), ferret (He et al 2002), and dog (Dyce et al 2010). Voss & Jansa (2009) reported presence of the jugal bone in the marsupial Marmosa murina. However, in this study we have not identified the jugal and mastoid bones.…”
Section: Discussionmentioning
confidence: 95%
“…The hard palate is perforated by foramina and fenestrae. According to Voss & Jansa (2009), these foramina and fenestrae exhibit considerable variation in occurrence,…”
Section: Discussionmentioning
confidence: 99%
“…Laboratory Methods: We extracted DNA from preserved tissues or dried museum specimens using methods described in Voss and Jansa (2009) and Giarla et al (2010). To minimize risk of contamination, all extractions from museum specimens were performed in an isolated laboratory where mammalian polymerase chain reaction (PCR) products were not present.…”
Section: Introductionmentioning
confidence: 99%
“…To minimize risk of contamination, all extractions from museum specimens were performed in an isolated laboratory where mammalian polymerase chain reaction (PCR) products were not present. We PCR-amplified six loci for this study (CYTB, BRCA1, IRBP, OGT, SLC38, and Anon128) using the primers listed in appendix 2 and methods described in Voss and Jansa (2009), Giarla et al (2010Giarla et al ( , 2014, Gutiérrez et al (2010), and Pavan et al (2014). The resulting PCR products were Sanger-sequenced on an ABI 3730xl automated sequencer.…”
Section: Introductionmentioning
confidence: 99%