Organizer for Reading: 5 – 4 – 3 – 2 – 1 5 Key words from the text 1. 2. 3. 4. 5. 4 Facts related to the main topic 1. 2. 3. 4. 3 New words 1. 2. 3. 2 Facts you already knew 1. 2. 1 Question you still have http://www.princeton.edu/~chm333/2004/Bioremediation/Hydrocarbons.htm Hydrocarbons Where does hydrocarbon contamination come from? Hydrocarbons can be introduced into the environment via incomplete combustion of fossil fuels, accidental discharge during transport, the disposal of petroleum products and other organic wastes, incineration of refuse and wastes, and various industrial processes. They can also be produced as a result of natural processes including forest fires and volcanic eruptions. Certain hydrocarbons known as polycyclic aromatic hydrocarbons (PAHs) are found in soil at wood preservation plants and gas manufacturing facilities. Why are hydrocarbons toxic? The inertness of high molecular weight hydrocarbons coupled with low solubility in water and strong lipophilic character lead to high accumulation levels and persistence. Some hydrocarbons (such as benzene) have been shown to be carcinogenic. In the case of large industrial oil spills, the oil can actually suffocate living organisms and destroy entire ecosystems. Excess hydrocarbons in aqueous environments can deplete the supply of oxygenating molecules, leading to anoxic conditions. Why use bioremediation? Although they can be eliminated abiotically through photooxidation, PAHs with more than three rings are more difficult to remove. High-molecular weight PAHs have a low bioavailability due to their strong adsorption onto the soil organic matter, high resonance energy, and toxicity. Numerous microorganisms – bacteria, algae, and fungi – are capable of metabolizing hydrocarbons. http://www.princeton.edu/~chm333/2004/Bioremediation/HOS%20main.htm Halogenated Organic Solvents The halocarbons, both halogenated compounds and halogenated solvents, are widespread pollutants found in air, water, soil, and sediment; they are recalcitrant molecules resistant to mineralization because the carbon-halogen bond is so stable. The stability and chemical inertness of many halogenated compounds is part of their appeal in many industrial processes, however it also makes them slow to degrade once they are released into the environment. In general, the more halogens there are on a molecule, the slower the degradation process. The focus for bioremediation of halocarbons is to exploit ability of organisms that have the natural capacity to mineralize these toxic contaminants into benign molecules. Halogenated organic solvents have a wide range of uses including metal processing, electronics, dry cleaning and paint, paper and textile manufacturing. They thus have the potential to contaminate almost every aspect of the environment, particularly water and soil. Since halogenated solvents are generally denser than water they tend to sink and accumulate in groundwater sources (they are also known as DNAPLs or dense nonaqueous phase liquids.) Acute overexposure to halogenated solvents has serious health consequences for humans, including possible nervous system damage, heart failure, and increased rates of cancer. At lower doses halogenated solvents are considered potential carcinogens for humans and have been shown to cause cancer in laboratory animals. (Prince, 1998) http://www.princeton.edu/~chm333/2004/Bioremediation/HOC%20main.htm Halogenated Organic Compounds The halocarbons, both halogenated compounds and halogenated solvents, are widespread pollutants found in air, water, soil, and sediment; they are recalcitrant molecules resistant to mineralization because the carbon-halogen bond is so stable. The stability and chemical inertness of many halogenated compounds is part of their appeal in many industrial processes, however it also makes them slow to degrade once they are released into the environment. In general, the more halogens there are on a molecule, the slower the degradation process. The focus for bioremediation of halocarbons is to exploit ability of organisms that have the natural capacity to mineralize these toxic contaminants into benign molecules . Halogenated compounds have been used for a variety of purposes for hundreds of different industrial processes over the last 50 years. However they present a danger to human health and include such known toxins and potential carcinogens as dioxins, pesticides and PCBs. One prevalent example of a halogenated organic compound is the widely used pesticide DDT, which has been shown to bioaccumulate in animal fat tissue, disrupt hormone function, and damage ecosystems. PCB’s, polychlorinated biphenyls, are another type of halogenated organic compound that have a variety of industrial applications as coolants, lubricants, plasticizers, and dies. PCB’s are toxic chemicals and exposure has been shown to cause cancer in laboratory studies. PCB’s may also adversely effect human health by contributing to neurological, immune system, reproductive system, and other organ damage (see the EPA for more detail on PCB health effects ). A major problem with halogenated compounds is that they belong to a class of molecules known as POP’s, persistant organic pollutants, which tend to biodegrade very slowly. It was originally thought that there were no natural sources of halogenated compounds in the environment, and hence no organisms that had evolved to exploit them. However, it has recently been shown that this is not the case (organisms as well as volcanic eruptions can produce these compounds,), and that natural production of chlorinated phenols may actually be greater than anthropogenic sources. Since these compounds have in fact existed for millions of years, there are naturally occurring strains of bacteria have evolved to break down halogenated compounds, thus opening up the possibility for bioremediation treatment of contaminated sites. http://www.princeton.edu/~chm333/2004/Bioremediation/NON%20main.htm Nonchlorinated Herbicides and Pesticides The bioremediation of herbicides and pesticides is of practical use, as it offers a less expensive and more environmentally friendly way of cleaning up potential problems associated with the toxins. The process focuses on detoxification rather than waste translocation [Dzantor], thereby reducing the cost and complications associated with the possible alternatives, such as offsite movement of the chemicals, human exposure, and expensive disposal of contaminated soil as hazardous waste [Moorman]. When pesticides, herbicides, and fungicides are applied correctly they are usually designed to be biodegradable so that they do not accumulate in the food chain. However, when these chemicals are introduced to the environment in large quantities from manufacturing, storage or spills they do present a contamination problem. Furthermore some nonchlorinated pesticides and herbicides may contaminate the water supply and pose a potential health hazard. Contamination can also result from heavy rain fall in the spring that washes away pesticide and herbicide residue from newly treated fields into streams. Bioremediation strategies can be employed to mineralize these compounds at contaminated sites. A contamination in drinking water can cause serious consequences, even to those who do not immediately drink that particular water. The problem can quickly jump from phytoplankton feeding on the contaminated water to humans, in just a few short steps (phytoplankton to clams to fish to humans). Thus, the managing of storage and spills of toxins such as pesticides and herbicides is critical to several different species. http://www.princeton.edu/~chm333/2004/Bioremediation/Nitrogen%20Compounds.htm Nitrogen Compounds Sources of Nitrogen contamination: Nitrogen contamination in the form of nitrate (NO3-) and ammonia (NH3) occurs as a result of agricultural runoff from fertilizer or animal waste. It is highly soluble and easily percolates through the soil, contaminating aquifers. This excess nitrate poses a problem since it leads to eutrophication in streams and has some averse health effects in humans. Nitrogen contamination also exists in the form of nitroaromatic compounds such as nitrobenzene, nitrophenol, nitrotoluene, and nitrobenzoate which are used in the industrial manufacture of pesticides, explosives, dyes, pharmeceuticals and plastics. Trinitrotoluen (TNT) Health problems: Nitrate ingestion can cause blue-baby syndrome (methaemoglobinemia) since nitrate-reducing bacteria in the intestine produce nitrite which bind with hemoglobin in blood. This inhibits the red-blood cells from transporting oxygen to tissue cells. Nitroaromatics are also highly toxic as they are mutanagenic, and carcinogenic. Why use bioremediation? Bioremediation of nitrogenous pollution is not a new idea; the decontamination of nitrate and ammonia pollution by bacteria is a major part of the nitrogen cyle. In fact, wastewater treatment plants take advantage of this biological process all the time to remove nitrogenous pollution from water via aeration tanks - we simply don't usually label this process as bioremdiation. Furthermore, wastewater treatment is an example of ex situ treatment since the contaminated media is transported to a different location for remediation. While this treatment is effective, it requires expensive machinery and pump systems. Thus much current research is investigating potential strategies for in situ remediation. http://www.princeton.edu/~chm333/2004/Bioremediation/Metals.htm Metals Metal contamination: A variety of metal contaminents exist in groundwater, surface water, and soils resulting from industrial and agricultural activity. Toxic metals such as lead, mercury, cadmium, arsenic, chromium, and uranium can cause damage to human health and the environment. How does metal contamination occur? Perhaps the most prevalent and problematic form of metal pollution is acid mine drainage. This occurs when the mining of coal and metal ores exposes metals and radionuclides to the atmosphere allowing them to be oxidized by certain bacteria (Thiobacillus ferrooxidans). For example pyrite (often exposed in coal mining) can be oxidized to iron hydroxide and sulfuric acid: FeS2 + 15/4 O2 + 7/2 H2O = Fe(OH)3 + 2H+ + 2HSO4The effluent produced, known as acid mine drainage, is highly toxic since it is not only acidic but also contains toxic metals. Such effluents have been known to contaminate nearby watersheds, killing much of the aquatic life. Streams containing acid mine effluent (pictured below) are often discolored due to Fe(OH)3 or “ yellow-boy” contamination. Why use bioremediation? While metals cannot be broken down into non-toxic components like organic compounds, bioremediation can be used to stabalize, extract, or reduce the toxicity of soil and groundwater contaminated by acid mine drainage. Bioremediation strategies are often more beneficial than traditional "pump and treat" strategies because it can be implemented in situ, providing a simpler, less intrusive, and cheaper method of remediation.