Water tanks of bromeliads are dynamic and complex environments inhabited by communities of different organisms including endemic species (Benzing, 1990;Lopez et al., 2009;Whittman, 2000). The presence of trapped water and organic detritus (phytotelmata) in tanks formed in bromeliad leaf rosettes is a major source of nutrients for these organisms and communities associated with the phytotelmata (Richardson et al., 2000). Hagler et al. (1993) isolated, from phytotelmata of the bromeliad Quesnelia quesneliana in the Coroa Grande mangrove, Rio de Janeiro, two cultures that were identified by physiological and morphological tests as Saccharomyces unisporuslike. Araú jo et al. (1998) isolated additional strains of the same yeast from water tanks of five bromeliad species in mangroves, rain forest and coastal sand dune ecosystems of Rio de Janeiro. Sequence analysis of the D1/D2 regions of the large subunit of the rRNA gene showed that these strains belong to the genus Kazachstania. The novel species, Kazachstania bromeliacearum sp. nov., is proposed to accommodate these isolates.Water samples from tanks of five bromeliad species, Q. quesneliana, Nidularium procerum, Neoregelia cruenta, Aechmea nudicaulis and Vriesia procera, were collected from sites in the mangrove of Coroa Grande, a swamp located in the Atlantic Forest Ecological Reserve of Poço das Antas and in the sand dune area of Maricá. All collection sites were located in the state of Rio de Janeiro, Brazil. Collections were done between January 1990 and September 1997. Water samples were collected aseptically with a sterile pipette and transferred to sterile flasks that were transported to the laboratory on wet ice for processing within 8 h. Aliquots of 0.1 ml of appropriate decimal dilutions were spread on YM agar supplemented with 0.04 % chloramphenicol (Yarrow, 1998). The plates were incubated at 25 u C for 3 to 8 days and selected colonies were purified and maintained on 1 % glucose, 0.5 % yeast extract, 0.5 % malt extract, 0.2 % mono sodium phosphate and 2 % agar (GYMP) agar slants or in liquid nitrogen for later identification. The yeasts were characterized by standard methods (Yarrow, 1998), and identification followed the keys of Kurtzman & Fell (1998). The rDNA internal transcribed spacer (ITS) region was amplified by PCR using ITS1 and ITS4 primers and the number of base pairs was estimated on an agarose gel (Valente et al., 1996). The D1/D2 domains of the large subunit rRNA gene Abbreviation: ITS, internal transcribed spacer.The GenBank/EMBL/DDBJ accession number for the D1/D2 domain sequence of the large subunit of the rRNA gene of strain IMUFRJ 51496 T is HQ412595.