Methane recovery efficiency in a submerged anaerobic membrane bioreactor (SAnMBR) treating sulphate-rich urban wastewater: Evaluation of methane losses with the effluent

The present paper presents a submerged anaerobic membrane bioreactor (SAnMBR) as a sustainable approach for urban wastewater treatment at 33 and 20 C, since greenhouse gas emissions are reduced and energy recovery is enhanced. Compared to other anaerobic systems, such as UASB reactors, the membrane technology allows the use of biogas-assisted mixing which enhances the methane stripping from the liquid phase bulk. The methane saturation index obtained for the whole period (1.00 ± 0.04) evidenced that the equilibrium condition was reached and the methane loss with the effluent was reduced. The methane recovery efficiency obtained at 20 C (53.6%) was slightly lower than at 33 C (57.4%) due to a reduction of the treatment efficiency, as evidenced by the lower methane production and the higher waste sludge per litre of treated wastewater. For both operational temperatures, the methane recovery efficiency was strongly affected by the high sulphate concentration in the influent wastewater.This research work has been supported by the Spanish Research Foundation (CICYT Projects CTM2008-06809-C02-01 and CTM2008-06809-C02-02) and the Comunidad Valenciana Regional Government (GVACOMP2009-285), which are gratefully acknowledged.Gimenez, J.; Martí, N.; Ferrer, J.; Seco, A. (2012). Methane recovery efficiency in a submerged anaerobic membrane bioreactor (SAnMBR) treating sulphate-rich urban wastewater: Evaluation of methane losses with the effluent. Bioresource Technology. 118:67-72. https://doi.org/10.1016/j.biortech.2012.05.019S677211

The ‘hot zone policy’ for colorectal cancer screening presents unique risks and opportunities for rural Australia

Objective: Colorectal cancer has geographic inequities in Australia, with higher mortality rates and lower participation in the National Bowel Cancer Screening Program (NBCSP) in remote and rural areas. The at-home kit is temperaturesensitive, necessitating a ‘hot zone policy’ (HZP); kits are not sent when an area's average monthly temperature is above 30°C. Australians in HZP areas are susceptible to potential screening disruptions but may benefit from well-timed interventions to improve participation. This study describes the demographics of HZP areas and estimates the impacts of potential screening changes. Methods: The number of individuals in HZP areas was estimated, as well as correlations with remoteness, socio-economic and Indigenous status. The potential impacts of screening changes were estimated. Results: Over a million eligible Australians live in HZP areas, which are more likely to be remote/rural, have lower socio-economic status and higher Indigenous populations. Predictive modelling estimates that any 3-month screening disruption would increase CRC mortality rates up to 4.1 times more in HZP areas vs unaffected areas, while targeted intervention could decrease mortality rates 3.4 times more in HZP areas. Conclusion: People living in affected areas would be negatively impacted by any NBCSP disruption, compounding existing inequities. However, well-timed health promotion could have a stronger impact.Joachim Worthington, Jie-Bin Lew, Emily He, Kate Broun, Katina D'Onise, Paul Grogan, Karen Canfell, Eleonora Felett

Experimental study of the anaerobic urban wastewater treatment in a submerged hollow-fibre membrane bioreactor at pilot scale

The aim of this study was to assess the effect of several operational variables on both biological and separation process performance in a submerged anaerobic membrane bioreactor pilot plant that treats urban wastewater. The pilot plant is equipped with two industrial hollow-fibre ultrafiltration membrane modules (PURON¿ Koch Membrane Systems, 30m 2 of filtration surface each). It was operated under mesophilic conditions (at 33°C), 70days of SRT, and variable HRT ranging from 20 to 6h. The effects of the influent COD/SO 4-S ratio (ranging from 2 to 12) and the MLTS concentration (ranging from 6 to 22gL -1) were also analysed. The main performance results were about 87% of COD removal, effluent VFA below 20mgL -1 and biogas methane concentrations over 55% v/v. Methane yield was strongly affected by the influent COD/SO 4-S ratio. No irreversible fouling problems were detected, even for MLTS concentrations above 22gL -1. © 2011 Elsevier Ltd.This research work has been supported by the Spanish Research Foundation (CICYT Projects CTM2008-06809-C02-01 and CTM2008-06809-C02-02), which is gratefully acknowledged.Giménez García, JB.; Robles Martínez, Á.; Carretero Martin, L.; Durán Pinzón, F.; Ruano García, MV.; Gatti, MN.; Ribes Bertomeu, J.... (2011). Experimental study of the anaerobic urban wastewater treatment in a submerged hollow-fibre membrane bioreactor at pilot scale. Bioresource Technology. 102(19):8799-8806. doi:10.1016/j.biortech.2011.07.014S879988061021

Sensitive and specific detection of proviral bovine leukemia virus by 5' Taq nuclease PCR using a 3' minor groove binder fluorogenic probe

Sensitive assays are required to detect proviral bovine leukemia virus (BLV) in donor cattle used for the in vivo preparation of Australian tick fever vaccines. 5' Taq nuclease assays using 3' minor groove binder DNA probes (TaqMan®MGB) were developed and compared to conventional PCR assays for sensitive detection of Australian BLV. Seven beef and dairy herds were screened using DNA prepared by a variety of protocols to evaluate these tests. Comparative sensitivities of PCR tests were determined by testing log10 dilutions of plasmids with inserted BLV sequences. Animals were also screened by the BLV standard agar-gel immunodiffusion test (AGID) and commercial enzyme linked immunosorbent assays (ELISA) for antibodies, and an ELISA for detecting viral antigens expressed (VAE) in lymphocyte cultures. The TaqMan®MGB assay based on the pol region was the most sensitive and specific for the detection of BLV. This is the first report of a sensitive BLV 5' Taq nuclease assay

Detection of Eimeria acervulina using the polymerase chain reaction

A polymerase chain reaction (PCR)-based assay was developed for the detection of Eimeria acervulina. Primers were designed to amplify a fragment of the EASZ240/160 sporozoite antigen gene. The PCR assay detected as few as 10 E. acervulina oocysts in a mixed population containing a total of 10(6) oocysts. No nonspecific reaction was observed with any other species of avian Eimeria known to occur in Australia. PCR products from genomic DNA were 237 bp larger than predicted from previously reported cDNA sequences. Sequencing of the product revealed the presence of a probable intron. This work demonstrates the potential of PCR-based assays for identification and detection of avian Eimeria. Potential uses include identification of minor species present in mixed infections and quality control in the production of live vaccines

Relationships between vaccine and virulent strains of Babesia bovis during co-infection in calves

No abstract availabl