Microbiotheria Ameghino, 1889
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https://doi.org/10.1206/0003-0090.457.1.1 |
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https://treatment.plazi.org/id/03EFDD5D-F6DB-68CB-DACE-FABA1B28FEDC |
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Felipe (2022-08-07 14:35:17, last updated 2022-08-07 15:29:28) |
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Microbiotheria Ameghino, 1889 |
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CONTENTS: Dromiciops (fig. 43) and † Microbiotherium .
STEM AGE: 45.6 Mya (95% HPD: 41.4–48.8 Mya).
CROWN AGE: 17.3 Mya (95% HPD: 14.0–21.8 Mya).
UNAMBIGUOUS CRANIODENTAL SYNAPOMOR- PHIES: Basisphenoid with a distinct sagittal keel (char. 48: 0→1; ci = 1.000); auditory bulla large,
33 But see Kealy and Beck (2017: 15) regarding anomalous relationships recovered in the molecular analysis of May-Collado et al. (2015).
contacting rostral process of petrosal (char. 55: 1→2; ci = 0.300); caudal and rostral tympanic processes of petrosal seamlessly fused, forming a petrosal plate (char. 68: 0→2; ci = 0.154); and five upper incisors present (char. 103: 2→0; ci = 0.333).
COMMENTS: Of the four unambiguous morphological synapomorphies supporting monophyly of Microbiotheria (equivalent to Microbiotheriidae in our analyses), two occur homoplastically in other marsupial groups and one appears questionable because it is a reversal in the number of upper incisors from three back to the ancestral metatherian complement of five. However, presence of a basiphenoid with a distinct sagittal keel is a distinctive cranial apomorphy that is apparently unique to microbiotherians (Hershkovitz, 1992a; 1999; Giannini et al., 2004; Wible et al., 2018). Although several genera of fossil microbiotherians are known from South America (Marshall, 1982; Goin and Abello, 2013; Goin et al., 2016), all except † Microbiotherium (for which cranial material, including a specimen [MACN A 8505] preserving the part of the basisphenoid sagittal keel, is known; Segall, 1969b; Marshall, 1982) are known from dental remains only.
As already discussed (see Australidelphia above), the oldest definitive member of the order described to date is probably the woodburnodontid † Woodburnodon casei from the Cucullaea I Allomember of the La Meseta Formation, Seymour Island, off the Antarctic Penninsula. Based on current evidence, the age of † W. casei appears to be ~40 Mya (Douglas et al., 2014; Amenábar et al., 2019; Mörs et al., 2020). Most recent studies have concluded that the early or middle Palaeocene † Khasia cordillerensis is not a member of Microbiotheria ( Oliveira and Goin, 2006; Goin et al., 2016; Carneiro et al., 2018; but see Muizon et al., 2018), and putative microbiotherian specimens reported from the early Eocene Las Flores Fauna (Goin, 2003; Zimicz, 2012; Woodburne et al., 2014a; Goin et al., 2016) have yet to be formally described (see Australidelphia above).
Oliveira, E. V., and F. J. Goin. 2006. Marsupiais do inicio do Terciario do Brasil: origem, irradiacao e historia biogeografica. In N. C. Caceres and E. L. A. Monteiro Filho (editors), Os Marsupiais do Brasil: biologia, ecologia e evolucao: 299 - 320. Campo Grande: UFMS.
Segall, W. 1969 b. The middle ear region of Dromiciops. Acta Anatomica 73: 489 - 501.
Wible, J. R., S. L. Shelley, and G. W. Rougier. 2018. The mammalian parasphenoid: Its occurrence in marsupials. Annals of Carnegie Museum 85 (2): 113 - 164.
Woodburne, M. O., et al. 2014 a. Revised timing of the South American early Paleogene land mammal ages. Journal of South American Earth Sciences 54: 109 - 119.
Zimicz, A. N. 2012. Ecomorfologia de los marsupiales paleogenos de America del Sur. Ph. D. dissertation, Facultad de Ciencias Naturales y Museo, Universidad Nacional de La Plata, La Plata.
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