2006
DOI: 10.1644/05-mamm-a-386r1.1
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Home-Range and Activity Patterns of the South American Subterranean Rodent Ctenomys Talarum

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Cited by 84 publications
(77 citation statements)
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References 65 publications
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“…Although fluctuations in T a within the burrows are buffered in relation to surface T a s (9.5 ± 2.9°C during winter, 29.1 ± 2.7°C during summer; Cutrera and Antinuchi 2004), individuals are also exposed to aboveground T a variation, since surface exploration is common during their regular, but short, bouts to gather food near the burrow 0 s openings (see Luna and Antinuchi 2003;Antinuchi et al 2007), or during dispersal periods (Malizia et al 1995). Therefore, the inability to increase both coldinduced MMR and NST in C. talarum after cold acclimation suggest that extreme T a s do not represent a challenge for individuals when they are aboveground, allowing an arrhythmic pattern of activity outside the burrows throughout the day (Luna et al 2000;Cutrera et al 2006). …”
Section: Discussionmentioning
confidence: 99%
“…Although fluctuations in T a within the burrows are buffered in relation to surface T a s (9.5 ± 2.9°C during winter, 29.1 ± 2.7°C during summer; Cutrera and Antinuchi 2004), individuals are also exposed to aboveground T a variation, since surface exploration is common during their regular, but short, bouts to gather food near the burrow 0 s openings (see Luna and Antinuchi 2003;Antinuchi et al 2007), or during dispersal periods (Malizia et al 1995). Therefore, the inability to increase both coldinduced MMR and NST in C. talarum after cold acclimation suggest that extreme T a s do not represent a challenge for individuals when they are aboveground, allowing an arrhythmic pattern of activity outside the burrows throughout the day (Luna et al 2000;Cutrera et al 2006). …”
Section: Discussionmentioning
confidence: 99%
“…The mtDNA has non-recombinant maternal inheritance, which allows the retention of haplotypes shared between populations recently isolated, or to keep the differentiation between populations in recent secondary contact that had previously differentiated in allopatry. Whereas, male-biased dispersal, that is characteristic of the species of the genus (Malizia and Busch, 1991;Cutrera et al, 2006), can lead to faster and farther dissemination of alleles of nuclear molecular markers relative to mtDNA, and associated with the nuclear genome recombination and high mutation rates of microsatellite loci, it can mask the signals of historical evolutionary processes in the nuclear genome (Petit and Excoffier, 2009;Yang and Kenagy, 2009). …”
Section: Geographical Barriersmentioning
confidence: 99%
“…This little effect of maternal odors on food choice observed in tuco-tucos contrasts to what was observed in more social lagomorph and rodent species, like O. cuniculus (Bilkó et al 1994;Altbäcker et al 1995;Hudson et al 1999) and R. norvegicus (Galef and Beck 1985;Laland and Plotkin 1991;Galef 1998). These species, whose dietary preferences are to a certain extent socially transmitted, differ from tuco-tucos in their behavioral and ecological traits, e.g., they are cursorial species that have gregarious habits (Wilson and Reeder 2005) and, by contrast, C. talarum is a solitary subterranean rodent (Cutrera et al 2006). These facts suggest that individual learning, rather than social learning mediated by maternal odors, might explain the development of food preferences in our experiment.…”
Section: Discussionmentioning
confidence: 75%
“…We did not manipulate mother's diet before odor collection in order to reflect changes in pup's dietary preferences, so close to what happens in free-living animals. We only tested maternal odors because freeliving Los Talas' tuco-tucos are solitary (Cutrera et al 2006), and pups rely exclusively on maternal care to survive (Zenuto et al 2001). …”
Section: Collection Of Odor Samplesmentioning
confidence: 99%