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Chloroform in the environment: occurrence, sources, sinks and effects
1School of Chemistry, University of Bristol, UK. archie@marbury.u-net.com
Chemosphere
|February 15, 2003
Summary
Chloroform environmental flux is constant, primarily from natural sources like seawater and soil. Despite widespread presence, it poses no significant ecotoxicological risk or ozone depletion threat.
Area of Science:
- Environmental Chemistry
- Atmospheric Science
- Ecotoxicology
Background:
- Chloroform (CHCl3) is a volatile organic compound with both natural and anthropogenic sources.
- Understanding its environmental flux and fate is crucial for assessing ecological and atmospheric impacts.
Purpose of the Study:
- To quantify chloroform emissions from various environmental sources.
- To determine chloroform's atmospheric concentration, distribution, and removal processes.
- To evaluate the ecotoxicological risks and atmospheric effects of chloroform.
Main Methods:
- Quantification of chloroform flux from oceanic and terrestrial sources.
- Atmospheric modeling to determine distribution and concentration.
- Assessment of environmental partitioning and degradation pathways.
Main Results:
- Total environmental chloroform flux is approximately 660+/-220 Gg/yr, with 90% from natural origins (offshore seawater and soil processes).
- Anthropogenic sources contribute 66+/-23 Gg/yr, mainly from industrial oxidation of organic matter.
- Chloroform predominantly partitions to the atmosphere (>99%), with an average concentration of 18.5 pmol/mol; atmospheric oxidation balances emissions.
- No significant ecotoxicological risk was found, even for sensitive aquatic life stages.
- Chloroform does not materially deplete ozone or act as a photochemically active VOC, with a low global warming potential.
Conclusions:
- Natural processes dominate chloroform emissions, with significant contributions from marine and soil environments.
- Current environmental concentrations of chloroform do not pose a substantial risk to ecosystems or human health.
- Chloroform's limited stratospheric transport and low photochemical reactivity mean it has negligible impact on ozone depletion and climate change.