Abstract:
The aim of current experimental work was to explore the importance of microbial
mat present at the mangrove area of Sandspit backwaters, Karachi. The first chapter consists
of an introduction to mangroves in general. In chapter 2, nutrients in the backwater channels
were studied. It was found that nutrient levels were more on site where mat was present as
compared to without mat site. Overall phosphate levels were high throughout all seasons and
the nutrient levels were found in the following order phosphate>ammonium>nitrate>nitrite.
In chapter 3, it was observed that the presence or absence of microbial mat directly influence
the soil. The soil covered with mat have increased water retention, low salinity and pH, high
carbon as compared to soil without mat. In chapter 4, the seasonal rates of potential
nitrification were examined. This process is a significant step in nitrogen cycle and involves
the conversion of ammonium into nitrate. Although there were no drastic changes in rates
with respect to seasons, the presence of microbial mat significantly affects the rates of
potential nitrification. In chapter 5, microbial mats were surveyed. The primary members of
mat include few protozoa, cyanobacteria, bacteria and diatoms. The filamentous forms of
cyanobacteria were responsible for macroscopic green sheath formation on top soil.
Phormidium tenue, Spirulina labyrinthiformis, Spirulina major, Oscillatoria limosa,
Phormidium breve and Oscillatoria prínceps were present in all seasons. In chapter 6,
cyanobacterial metabolites were inspected. Seawater fraction of Aphanocapsa litoralis and
ethanol fraction of Phormidium breve were active against Candida albicans. Phormidium
breve extract was more cytotoxic (LC50 0.02 mg/ml) against Artemia salina as compared to
Aphanocapsa litoralis extract (LC50 6.2 mg/ml). In chapter 7, metabolites of bacteria
associated with microbial mat were screened. Out of 120 isolates only two isolates SSC1407
(Proteus sp.) and SSC14011 (Klebsiella pneumoniae strain) were found to have some
antagonistic activity against isolates of E. coli and Proteus O respectively. SSC1407
tolerated increased levels of temperature and different types of chemicals. SSC14011
tolerated high pH, UV-rays and also produced higher protein yield after successive
purifications. SSC14011 was slightly more cytotoxic (LC50 0.046 mg/ml) against Artemia
salina than SSC1407 (LC50 0.052mg/ml).