Keep in mind Mycoremediation is still an experimental technology. If you end up deciding to start your own project, we are happy to provide cultivation advice and spawn, but we cannot guarantee that it will reduce contamination.
To read the methods and results of past experiments using Mycoberms to create an inoculated drain field, see the online article A Novel Approach to Farm Waste Management. For hydrocarbon remediation strategies; The Petroleum Problem. I attached more information on our study with the Washington Department of Transportation [link].
Our Pleurotus ostreatus is the same strain we used for our MycoBooms. Another species we have found to be very useful in remediation is Stropharia rugoso-annulata Wood Chip Spawn. You may want to consider utilizing both species and comparing them side by side. Oyster mushrooms have been shown to be capable of metal hyper-accumulation, though they can be more challenging to cultivate outdoors on a remediation-scale level than Stropharia. While the species we use are edible, we do not recommend consuming mushrooms that have been used for Mycorestoration.
Further experiments have been done to assess the removal of bacteria by such bags of myceliated wood chips; research results are available in our online article Mycofiltration Enters the Commons. Be sure to read and share the attached reports:
http://fungi.com/pdf/articles/Fungi_Perfecti_Phase_I_Report.pdf
http://www.sciencedirect.com/science/article/pii/S0925857414002250
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I have a couple of other references that may be helpful in your endeavors:
Our coworker, Alex Taylor, recently had his masters thesis manuscript published on Mycofiltration with Stropharia. You can read this here: http://www.mdpi.com/2073-4441/10/9/1226/htm
One of the most comprehensive sources for research done on Mycoremediation is by Harbhajan Singh entitled Mycoremediation: Fungal Bioremediation.
| Treatment | Criteria | Comment |
|---|---|---|
| Storage; ambient temperature 2–20 °C | 1.5–2 years | Will eliminate bacterial pathogens; regrowth of E. coli and Salmonella may need to be considered if rewetted; will reduce viruses and parasitic protozoa below risk levels. Some soil-borne ova may persist in low numbers. |
| Storage; ambient temperature >20–35 °C | >1 year | Substantial to total inactivation of viruses, bacteria and protozoa; inactivation of schistosome eggs (<1 month); inactivation of nematode (roundworm) eggs, e.g. hookworm (Ancylostoma/Necator) and whipworm (Trichuris); survival of a certain percentage (10–30%) of Ascaris eggs (≥4 months), whereas a more or less complete inactivation of Ascaris eggs will occur within 1 year. |