AI Article Synopsis

  • Antarctica has been seen as a pristine environment, but recent decades have revealed significant pollution due to human activities like oil spills and waste disposal, as well as natural sources like volcanic activity.
  • A microbiological study tested a bacterial consortium's ability to break down phenol in the presence of various heavy metal ions, revealing that these metals inhibited bacterial growth to different extents.
  • The findings indicated that aluminum had the least inhibitory effect while silver severely impacted bacterial activity, suggesting that the bacterial consortium could still be effective for phenol degradation at certain metal concentrations.

Article Abstract

Antarctica has often been perceived as a pristine continent until the recent few decades as pollutants have been observed accruing in the Antarctic environment. Irresponsible human activities such as accidental oil spills, waste incineration and sewage disposal are among the primary anthropogenic sources of heavy metal contaminants in Antarctica. Natural sources including animal excrement, volcanism and geological weathering also contribute to the increase of heavy metals in the ecosystem. A microbial growth model is presented for the growth of a bacterial cell consortium used in the biodegradation of phenol in media containing different metal ions, namely arsenic (As), cadmium (Cd), aluminium (Al), nickel (Ni), silver (Ag), lead (Pb) and cobalt (Co). Bacterial growth was inhibited by these ions in the rank order of Al < As < Co < Pb < Ni < Cd < Ag. Greatest bacterial growth occurred in 1 ppm Al achieving an OD of 0.985 and lowest in 1 ppm Ag with an OD of 0.090. At a concentration of 1.0 ppm, Ag had a considerable effect on the bacterial consortium, inhibiting the degradation of phenol, whereas this concentration of the other metal ions tested had no effect on degradation. The biokinetic growth model developed supports the suitability of the bacterial consortium for use in phenol degradation.

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Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC10920555PMC
http://dx.doi.org/10.1007/s42770-023-01215-8DOI Listing

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