A black-pigmented, aerobic actinobacterium, tolerant to ionizing radiation, designated BMG 825 T , was isolated from desert limestone dust in Tunisia. The strain grew within the temperature range 10-40 C, at pH 5.5-11.0 and in the presence of 2 % NaCl. The DNA G+C content was 75.7 mol%, and its cell-wall peptidoglycan contained meso-diaminopimelic acid. Sugars of whole-cell hydrolysates were galactose, glucose, and trace amounts of ribose and mannose. The predominant menaquinone was MK-9(H 4 ), and the major fatty acids were iso-C 16 : 0 and C 16 : 1 !7c. The polar lipid profile comprised phosphatidylcholine, phosphatidylinositol, diphosphatidylglycerol, phosphatidylethanolamine, hydroxyphosphatidylethanolamine and an unspecified glycolipid. 16S rRNA gene sequence analysis revealed that the strain fell into the genus Geodermatophilus, showing the highest similarity with Geodermatophilus poikilotrophus DSM 44209 T (99.1 %). DNA-DNA hybridization results, phylogenetic distinctiveness and phenotypic properties supported the classification of this strain as a representative of a novel species of the genus Geodermatophilus, for which the name Geodermatophilus pulveris sp. nov. is proposed. The type strain is BMG 825 T (=CECT 9003 T =DSM 46839 T ).Twenty species are currently described within the genus Geodermatophilus (Hezbri et al., 2015a), and several of these actinobacteria have been reported to be highly resistant to stresses known to give rise to reactive oxygen species such as gamma-radiation, UV and desiccation (Gtari et al., 2012; Hezbri et al., 2015a, b, c). The genome (Ivanova et al., 2010) and recently published proteogenome of Geodermatophilus obscurus (Sghaier et al., 2016) provided a close-up view of mechanisms permitting adaptation to environmental stresses, which are mainly pigmentation, catalase production and repair of double-strand breaks through the non-homologous end joining pathway.Strain BMG 825 T was isolated during an investigation about the dust microbial population in grooves in limestone cliffs from the Tunisian part of the Grand Erg Oriental (English: 'Great Eastern Sand Sea') in the Sahara desert. The sample collected initially was serially diluted in 0.85 % saline solution. Aliquots of each serial dilution were then spread on Luedemann medium (DSMZ medium 877) (Luedemann, 1968) and R2A agar (DSMZ medium 830) (Reasoner et al., 1979), and incubated at 28 C for about 3 weeks. Thereafter, a dry, black colony designated BMG 825 T was isolated. The culture was sub-cultivated on Luedemann medium at 28 C for 7 days. Following purification, the organism was maintained in glycerol (35 %, w/v) stocks at À80 C for further investigations. Strain BMG 825 T was routinely grown on GYM Streptomyces medium (DSMZ medium 65) at 28 C for testing the physiological and biochemical properties, except where mentioned.