Influence of flow velocity on the removal of faecal coliforms in horizontal subsurface flow constructed wetland.

In order to determine the influence of flow velocity on the removal of faecal coliforms (FC) in constructed wetlands (CWs), removal rate constants of FC (k(FC)) were studied at various flow velocities (u). Membrane filtration technique was used during analysis. Values of k(FC) were determined using Reed's equation of pathogen removal; the results were compared with the plug flow equation. According to Reed's equation, k(FC) values ranged from 1.6 day⁻¹ at a velocity of 4 m/day to 34.5 day⁻¹ at a velocity of 42.9 m/day. The removal rates correlated positively with flow velocity (r = 0.84, p < 0.05). On assuming a plug flow equation, removal rates constants ranged from 0.77 to 11.69 day⁻¹; a more positive correlation (r = 0.93, p < 0.05) was observed. Optimum removal rate constants were observed for the velocity ranging 36 to 43 m/day. Generally, the increase of flow velocity improved FC removal rate constants: implying that pathogen removals are influenced by diffusion of the microorganisms into the biofilms on CW media. The velocity dependent approach together with the plug flow equation is therefore proposed for incorporation in the design of CW in a tropical climate where temperature variations are minor.

Methanosarcina semesiae sp. nov., a dimethylsulfide-utilizing methanogen from mangrove sediment.

Methanosarcina semesiae MD1T (T = type strain), a novel obligately methylotrophic methanogenic archaeon is described. Strain MD1T was isolated from an enrichment on dimethylsulfide inoculated with mangrove sediment. The cells were irregularly coccoid, non-motile, 1.4+/-0.2 microm in diameter and stained Gram-positive. The catabolic substrates used included dimethylsulfide, methanethiol, methanol and methylated amines, but not acetate, formate, H2/CO2 or a combination of these substrates. When cells grown on dimethylsulfide were transferred to trimethylamine or methanol and vice versa, a lag phase was observed. The same lag phase occurred when cells grown on trimethylamine were transferred to methanol and vice versa, indicating that for each substrate different enzymes were induced. Fastest growth occurred within a temperature range of 30-35 degrees C and a pH of 6.5-7.5. Both Na+ and Mg2+ were required for growth, with maximum growth rates at 200-600 mM Na+ and 20-100 mM Mg2+. The cells exhibited specific growth rates (h-1) of 0.07+/-0.02, 0.15+/-0.04 and 0.18-/+0.05 on dimethylsulfide, methanol and trimethylamine, respectively. Analysis of the 16S rRNA gene sequence showed that strain MD1T was phylogenetically closely related to members of the genus Methanosarcina, but clearly differed from all described species of this genus (94-97% sequence similarity).