Treatment of flow-through trout aquaculture effluents in a constructed wetland

A study on effluent treatment with sub-surface flow (SF) constructed wetlands was conducted in a small commercial scale Bavarian (Germany) flow-through trout farm. Under limited spatial and financial conditions a most suitable wetland was constructed. The wetland treatment efficiency at high hydraulic loading rates during raceway runoff and cleaning situation in comparison to sedimentation as initial treatment method was examined.

The constructional solution involved the alteration of six existing sedimentation basins (SB) to SF horizontal flow constructed wetlands with a pre-sedimentation area. As constructional materials only local, cheaply available materials were used in order to reduce the costs. The SF wetland had high treatment efficiencies in the two operational modes examined. During cleaning situation at a hydraulic loading rate (HLR) of 13.6 m/day treatment efficiency for total suspended solids (TSS) was highest and reached 68%. While during raceway runoff situation total ammonia nitrogen (TAN) treatment efficiency of 88% overtopped the efficiency of the other nutrients examined at a HLR of 10.6 m/day. In both treatment situations the SF wetland efficiency was significantly higher than the effect of the SB. SF constructed wetlands treating high hydraulic loading rates accompanied with short retention times were effective on dissolved nutrient treatment only for TAN and nitrite nitrogen (NO₂–N), while other dissolved nutrients like nitrate nitrogen (NO₃–N) and phosphate phosphorous (PO₄–P) showed no or even negative treatment effects through the wetland passage. To reduce these nutrients, other treatment conditions or wetland configurations are needed.     

New real-time PCR tests for species-specific detection of Chlamydophila psittaci and Chlamydophila abortus from tissue samples

Chlamydophila psittaci and Chlamydophila abortus are the causative agents of avian chlamydiosis (psittacosis) and ovine enzootic abortion, respectively. Both pathogens are known to possess zoonotic potential. Due to their close genetic relatedness, direct and rapid species identification is difficult. In the present study, new real-time PCR assays are reported for both species. The tests are based on highly specific probes targeting the ompA gene region and were conducted as duplex PCRs including an internal amplification control. The Cp. psittaci assay successfully passed a proficiency test at national level. Examination of field samples revealed Cp. psittaci as the dominating species in birds, but also Cp. abortus in a few psittacines. Real-time PCR assays for species-specific detection of Cp. psittaci and Cp. abortus are suited for routine diagnosis, which renders them important tools for the recognition of outbreaks of psittacosis and ovine enzootic abortion.