06%), and Pleuronematida (0.03%). Thetis brine and Tyro brine had a relatively similar ciliate community composition, both of which were dominated by CHIR99021 amplicons that have Strombidium as the closest BLAST match in the GenBank nucleotide database (64% and 45%, of all amplicons, respectively). Other abundant taxon groups

shared by these two samples were Novistrombidium {Selleck Anti-infection Compound Library|Selleck Antiinfection Compound Library|Selleck Anti-infection Compound Library|Selleck Antiinfection Compound Library|Selleckchem Anti-infection Compound Library|Selleckchem Antiinfection Compound Library|Selleckchem Anti-infection Compound Library|Selleckchem Antiinfection Compound Library|Anti-infection Compound Library|Antiinfection Compound Library|Anti-infection Compound Library|Antiinfection Compound Library|Anti-infection Compound Library|Antiinfection Compound Library|Anti-infection Compound Library|Antiinfection Compound Library|Anti-infection Compound Library|Antiinfection Compound Library|Anti-infection Compound Library|Antiinfection Compound Library|Anti-infection Compound Library|Antiinfection Compound Library|Anti-infection Compound Library|Antiinfection Compound Library|Anti-infection Compound Library|Antiinfection Compound Library|buy Anti-infection Compound Library|Anti-infection Compound Library ic50|Anti-infection Compound Library price|Anti-infection Compound Library cost|Anti-infection Compound Library solubility dmso|Anti-infection Compound Library purchase|Anti-infection Compound Library manufacturer|Anti-infection Compound Library research buy|Anti-infection Compound Library order|Anti-infection Compound Library mouse|Anti-infection Compound Library chemical structure|Anti-infection Compound Library mw|Anti-infection Compound Library molecular weight|Anti-infection Compound Library datasheet|Anti-infection Compound Library supplier|Anti-infection Compound Library in vitro|Anti-infection Compound Library cell line|Anti-infection Compound Library concentration|Anti-infection Compound Library nmr|Anti-infection Compound Library in vivo|Anti-infection Compound Library clinical trial|Anti-infection Compound Library cell assay|Anti-infection Compound Library screening|Anti-infection Compound Library high throughput|buy Antiinfection Compound Library|Antiinfection Compound Library ic50|Antiinfection Compound Library price|Antiinfection Compound Library cost|Antiinfection Compound Library solubility dmso|Antiinfection Compound Library purchase|Antiinfection Compound Library manufacturer|Antiinfection Compound Library research buy|Antiinfection Compound Library order|Antiinfection Compound Library chemical structure|Antiinfection Compound Library datasheet|Antiinfection Compound Library supplier|Antiinfection Compound Library in vitro|Antiinfection Compound Library cell line|Antiinfection Compound Library concentration|Antiinfection Compound Library clinical trial|Antiinfection Compound Library cell assay|Antiinfection Compound Library screening|Antiinfection Compound Library high throughput|Anti-infection Compound high throughput screening| (30% in Tyro brine and 9% in Thetis brine), and Pseudotontonia (4% in Tyro brine and 8% in Thetis brine). While Laboea accounted for 11% of all amplicons in Thetis brine, this taxon group was absent in Tyro brine. A tintinnid ciliate taxon related to Salpingella as closest database relative occured exclusively in Tyro brine (4% of all amplicons), but not in Thetis (Additional file 3: Table S1). The ciliate community composition in Urania brine was dissimilar to

the brines in Tyro and Thetis basins. One striking quantitative difference was the high proportion of Pseudotontonia-related amplicons (40%) in Urania brine. However, while most of the relatively abundant taxon-groups were shared between these three brine samples (but in different quantities), most qualitative differences between Tyro, Thetis and Urania brines were attributed to taxon groups with lower abundances. Medee brine was distinct in its ciliate composition from other brines. Tyro interface stood out from the other interface samples. The most significant difference was the occurrence of 14,337 amplicons (41%), with Apocoleps HA-1077 order (Prorodontida) Vistusertib solubility dmso as the best BLAST match. The proportion of amplicons in Thetis, Urania and Medee interfaces related to this taxon was less

than 0.5%. Also the proportion of Strombidium-like amplicons in Tyro interface (40%) was decisively higher compared to the other interfaces (4-21%). Thetis interface and Urania interface had a very similar taxon composition, dominated by amplicons most closely related to Pleuronema (Pleuronematida) (70% in UIF and 57% in ThIF). This taxon was also highly represented in Medee interface (49%). The second most abundant taxon group in Medee interface were clevelandellids, represented with 43%. This taxon was underrepresented in the interfaces of other basins (0.02% in UIF – 4% in ThIF). Four taxa occured in all eight samples analyzed (closest BLAST matches: Pleuronema, Strombidium, Omegastrombidium, Apocoleps). Four taxa were exclusive to all interfaces (Palgiopyliella, Cyclidium, Schizocalpytra, Isochonida). Interestingly, not a single taxon occured exclusively in all brines simultaneously. However, 28 taxon groups were absent from interfaces but present in at least one of the brines. The same number of taxon groups was absent from all brines but occured in at least one of the interfaces. The majority of taxon groups had abundances accounting for less than 5% of all amplicons obtained within a sample.