2020
DOI: 10.1016/j.quascirev.2020.106282
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Taguatagua 1: New insights into the late Pleistocene fauna, paleoenvironment, and human subsistence in a unique lacustrine context in central Chile

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Cited by 19 publications
(11 citation statements)
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“…The crown clade Octodontidae differentiated in southern South America during the Late Miocene, over 10 My later than the divergence of the total clade Octodontidae from their sister family Ctenomyidae (Upham and Patterson 2012, 2015; Verzi et al 2014, 2016; Álvarez et al 2017). The time-calibrated phylogenies show that crown genera were already differentiated in the Pliocene (Table 1), yet their fossil record is limited mostly to the latest Pleistocene–Holocene (Massoia et al 1981; Simonetti 1989, 1994; Pearson and Pearson 1993; Massoia and Silveira 1996; Simonetti and Saavedra 1998; Teta and Ortiz 2002; Saavedra and Simonetti 2003; Saavedra et al 2003; Udrizar Sauthier et al 2009; Fernández et al 2016; López et al 2016; Labarca et al 2020; Tammone et al 2020). As an exception, Tympanoctomys is recorded in the Early Pleistocene (Ameghino 1889; Verzi et al 2002); in addition, Ameghino (1891) reported presence of Aconaemys in the “Pampeano inferior” (Pleistocene) of Córdoba based on mandibular remains and isolated teeth—these specimens being currently missing from the paleontological MACN collection.…”
Section: Discussionmentioning
confidence: 99%
“…The crown clade Octodontidae differentiated in southern South America during the Late Miocene, over 10 My later than the divergence of the total clade Octodontidae from their sister family Ctenomyidae (Upham and Patterson 2012, 2015; Verzi et al 2014, 2016; Álvarez et al 2017). The time-calibrated phylogenies show that crown genera were already differentiated in the Pliocene (Table 1), yet their fossil record is limited mostly to the latest Pleistocene–Holocene (Massoia et al 1981; Simonetti 1989, 1994; Pearson and Pearson 1993; Massoia and Silveira 1996; Simonetti and Saavedra 1998; Teta and Ortiz 2002; Saavedra and Simonetti 2003; Saavedra et al 2003; Udrizar Sauthier et al 2009; Fernández et al 2016; López et al 2016; Labarca et al 2020; Tammone et al 2020). As an exception, Tympanoctomys is recorded in the Early Pleistocene (Ameghino 1889; Verzi et al 2002); in addition, Ameghino (1891) reported presence of Aconaemys in the “Pampeano inferior” (Pleistocene) of Córdoba based on mandibular remains and isolated teeth—these specimens being currently missing from the paleontological MACN collection.…”
Section: Discussionmentioning
confidence: 99%
“…Approaches to Pleistocene-Holocene landscape reconstructions in southernmost South America follow this general trend, being mostly dominated by palynological, glaciological, and, more recently, geochemical evidence (e.g., Heusser, 2003;Moreno et al, 2012;Recasens et al, 2012;Borromei et al, 2018;Zolitschka et al, 2019). Certainly, a desirable goal is to increase the database of biological proxies, not only to gain a more accurate picture of environmental evolution, but also to understand how diverse biotic elements responded to past climatic changes (e.g., Labarca et al, 2020).…”
Section: Holocene Environmental Evolution In Cerro Benítez: Integrating Biological Evidencementioning
confidence: 98%
“…In Chile, several plant species bear fruits with the megafaunal dispersal syndrome; one such plant is the endemic vine Lardizabala biternata . In the present day, there are no large native vertebrates that consume its fruits (Figure 1); hence, it is presumed to have been dispersed by the extinct megafauna that was originally present along its area of distribution, which included Gomphotheriidae, Antifer ultra , and Hippidion principale (Labarca et al, 2020). The modern south Andean deer ( Hippocamelus bisulcus ) also roamed in the area where this vine is present, but it is absent today (Vila et al, 2005).…”
Section: Figurementioning
confidence: 99%