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. 2013 Jul 25;8(7):e69346.
doi: 10.1371/journal.pone.0069346. Print 2013.

Adaptation of pelage color and pigment variations in Israeli subterranean blind mole rats, Spalax ehrenbergi [corrected]

Affiliations

Adaptation of pelage color and pigment variations in Israeli subterranean blind mole rats, Spalax ehrenbergi [corrected]

Natarajan Singaravelan et al. PLoS One. .

Erratum in

  • PLoS One. 2013;8(8). doi:10.1371/annotation/27bebc65-09c5-4c58-be6c-4f22c4fe0919

Abstract

Background: Concealing coloration in rodents is well established. However, only a few studies examined how soil color, pelage color, hair-melanin content, and genetics (i.e., the causal chain) synergize to configure it. This study investigates the causal chain of dorsal coloration in Israeli subterranean blind mole rats, Spalax ehrenbergi.

Methods: We examined pelage coloration of 128 adult animals from 11 populations belonging to four species of Spalax ehrenbergi superspecies (Spalax galili, Spalax golani, Spalax carmeli, and Spalax judaei) and the corresponding coloration of soil samples from the collection sites using a digital colorimeter. Additionally, we quantified hair-melanin contents of 67 animals using HPLC and sequenced the MC1R gene in 68 individuals from all four mole rat species.

Results: Due to high variability of soil colors, the correlation between soil and pelage color coordinates was weak and significant only between soil hue and pelage lightness. Multiple stepwise forward regression revealed that soil lightness was significantly associated with all pelage color variables. Pelage color lightness among the four species increased with the higher southward aridity in accordance to Gloger's rule (darker in humid habitats and lighter in arid habitats). Darker and lighter pelage colors are associated with darker basalt and terra rossa, and lighter rendzina soils, respectively. Despite soil lightness varying significantly, pelage lightness and eumelanin converged among populations living in similar soil types. Partial sequencing of the MC1R gene identified three allelic variants, two of which were predominant in northern species (S. galili and S. golani), and the third was exclusive to southern species (S. carmeli and S. judaei), which might have caused the differences found in pheomelanin/eumelanin ratio.

Conclusion/significance: Darker dorsal pelage in darker basalt and terra rossa soils in the north and lighter pelage in rendzina and loess soils in the south reflect the combined results of crypsis and thermoregulatory function following Gloger's rule.

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Conflict of interest statement

Competing Interests: The authors have declared that no competing interests exist.

Figures

Figure 1
Figure 1. Map shows the studied populations of mole rats in Israel.
Kerem-Ben-Zimra, Alma and Rehaniya populations are located in Galilee mountains; Quneitra¸ A. Etan and Bental are in Golan heights. Muhraka and “Evolution Canyon” (Nahal Oren) populations are in Carmel mountains. Anza is located in West Bank, while Lahav is in Negev.
Figure 2
Figure 2. Patterns of variation across species of mole rats in Israel.
A) genetic variation, B) phenotypic variation, and C) environmental variation.
Figure 3
Figure 3. Pheomelanin/eumelanin ratio among Spalax populations across latitude.

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