Friday, December 29, 2006

Wiki spreadsheets, city budgets, wikicalc vs jot.com vs editgrid.com

The next wave of wiki's is out, and hallelujah, they don't (all / totally) suck. Here to say editgrid.com is fantastic.

Meet the contenders:

Let me spare you the details to start out with (besides, everything listed alphabetically puts editgrid in first anyhow)

editgrid.com: comin' at ya live from Hong Kong, this bad boy has it all. There's really not a good reason in my mind to review the other commercial piece (jot.com) except to trash it and save you the reader some troubles. EditGrid is amazing, uploaded an xls file with a couple thousand rows. Formatting - retained! Multiple tables in a spreadsheet? No Problem! EditGrid has it all. This is a straight up killer ap. Posted the entire city of Charlottesville line-item budget and voila! Up in a few minutes. Not surprisingly this cite is getting hit hard at the mooment, expect some delays while their netadmins deal with the reality of being excellent.

Jot.com (now google's love child, and prolly soon to move towards non-suck is a nice application that bites bytes). It's being revamped right now, this "lucky" author got to check it out pre-google, so there's no telling what the new release will do, check back in a few months, it's google, and it's bound to get better with some resources. So far however.... nothin' werked, as they say. Cut'n'Paste your spreadsheet and watch your computer crash and burn. No format retention and formulas don't work. This thing sucks


wikicalc : Dan Brinklin worked his way in to the geek hall of fame with visicalc almost 20 years ago. His new spreadsheet wikicalc is open source gpl, and so it gets some big points for that. Indeed with a decent server this may be a killer ap. It also has some decent cut'n'paste features, however it flakes out pretty hard on a serious data load. On the plus side it retains some formulas and can do formatting - WAY BETTER THAN JOT.COM and free open source! Even its alpha release is more inspiring than the jot.com crud.

Thursday, November 02, 2006

wikicalc, jotspot, charlottesville city budget

Wikicalc deserves some props for being a groovy open source spreadsheet wiki that's very decent for it's price, and works through some crucial bits of excel, so as to retain basic formulas and such.

With jot.com going to google.com last week there's another bunch of kids in the same playgroundsure to bring good attention to the arena where more transparent business practices can be developed, standardized, and optimized. Their product is sleek AJAX based and with calendar and location parsing technology built in this is one another slick development for the google folks.

And so that brings it around to the c-village 'hood skool. - charlottesville.jot.com - starting out with some of the non-general stuff, and working towards the line item morsels.

Tuesday, October 24, 2006

Carnegie Mellon Technology in the Arts

had a great time. Greeted at the entrance of CMU by a talking computer that seemed to recognize my lostness - "Do you need directions" came the metallic max headromesque voice.... I wasn't sure how advanced this computer was and assumed it was referring to direction in the sense of a few meters, as opposed to some greater direction in life....Anyhow, i responded yes about the time a friendly human concierge arrived to get me to the first meeting of the day. Not sure whether the human was controlled by the computer or whether it was of higher elegance... anyhow....

And as it happened the first meeting "Funding Technology Projects" was right down the hall. Met with Mr. Mackie of the Andrew Mellon Foundation - he is the head of Research in Technology Funding. He emphasized open source "if you're looking to spend on proprietary software look elsewhere" (http://www.mellon.org/research_it.html) and also emphasized use of open standards (The Mellon Foundation (along with MIT and others) funded dSpace, which is something we already ascribe to through Greenstone). **** If we're interested in collaborating on a school bus full of digitization equipment this would be the guy to talk to. they are playing with huge sums of money and we should really try to start something with them "if we fund you once we'll probably fund you again" -- in other words they like long term relationships.

Although initially slated to speak on Joomla's content management system (marshallrotc.org Virginia Verified Voting) when I got to looking at the schedule two other presenters wanted to cover Joomla and so I shifted my focus to Greenstone and IBM's analysis of wikipedia showing the underlying stability of the wiki format. Also met with Ellen Arnold, who invited me to be a grant reviewer for the Institute of Museum and Library Services (IMLS). I suspect this is a bit like being invited into the book of the month club, anyhow, I was earnestly flattered and accepted.


Otherwise enjoyed Pittsburgh a fair bit. Solid steel town, and affordable housing - imagine paying under 70K for a *solid* brick house? Went up Washington hill for the view, ate a hoagie, and went to a comic book convention across the street from my lodging. Very glad to be back, however must admit Pittsburgh is a most impressive and down to earth city. I also studied some of the requirements for funding in Pennsylvania, and would be glad to pass on some of that to the folks in Carlisle if they're not already well aware. The Bayer Foundation seemed very interested when I was talking about library->library services.

Saturday, July 01, 2006

sketch-up google earth


'nuf said. great software, fun and easy for architecture, stage, gis, and connected neatly to google earth. more on the projects @ http://www.rockbridgebusiness.com

Tuesday, June 13, 2006

Monetizing library records marc, usmarc, marcxml, marc 97 etc with Koha and the Liblime Enhancement

OK - started this a few months ago, and really not totally convinced Koha is gonna do what I need - neverthless it's worth a look if all you've got are a bunch of Marc Records. Greenstone.org's product, however, handles marc and a gajillion other formats....

The Enhanced Koha LibLime style is an amazing piece of code, picking up where the left of the geeksquads in dev land leave off - integrating a functional and user-friendly Amazon.com row into the matrix let's users "buy it now" from amazon while browsing through the collection in Koha gives libraries looking to justify digitizing their collections added incentive.

Getting Koha running can be a bit of work, depending on your operating system. IndexData does most of their work on Debian based systems (think Ubuntu) - and if you're running anything else it may take a few tries to get the whole thing running.

For a better understanding of the install process they have created a wiki and decent documentation.

Thursday, May 25, 2006

webhuddle - online whiteboard, collaboration tool, application desktop sharing, plus voip motherload hits the open source scene

Well it's been something I've been looking for forf a long long time - Webhuddle finally provides an open source VOIP + Desktop Sharing + Whiteboard software tool for the open source community. the developers are cool, and the forum is starting to take off. if this keeps up most websites will wiki+whiteboard their way through development processes plus database meetings and discussions for training. Most excellent. in case you were wondering... yeah - it's on sourceforge

Here's the author's tutorial on uploading content Working with webhuddle

Monday, April 10, 2006

Garlic Mustard / Alliaria petiolata / Alliaire officinale

Garlic Mustard / Alliaria petiolata / Alliaire officinale


A truly excellent friend in the Appalachian Spring and Summer - Garlic Mustard gives salads a bit of extra yum and good for ya too. Another invader - this one from Europe (Hungary and Chechoslovakia). It contains
alliarinoside - A unique anti-insectish glucoside, and several other isoflavones. It goes great with kudzu vinegar :)

Monday, April 03, 2006

more microdem + some white_dune

Anyhow, this week is back to 3d rendering in microdem and getting these GEOTIFF files to cooperate... also learning the joys and aches of white_dune - the open source VRML editor

ps for some really sweet Virtual Reality Markup Language (.wrl) files on the natch check out Peter Guth's (Microdem's Author) directory tree. http://www.usna.edu/Users/oceano/pguth/microdem/target3D/Buildings/

VRML Bridges, powerlines, buildings, tanks, aircraft, helicopters etc... totally badass - all in VRML 1.0 specification.

To convert these guys for white_dune (VRML 2 (some folks call it VRML97) you can use a nifty piece of software called Crossroads 3D if that's not doing it for you (it can drop out occasionally on large files) the vrml1 to vrml2 converter is a nice commandline utility that whoops.

Once you've got everything in VRML 2 (VRML 97) you can begin working in white_dune - the biggest challenge their is the preview window and moving objects around in there - if you've got a 3d mouse / joystick you may have more success and simplify your life - otherwise it's not bad.

Wednesday, March 29, 2006

lightscribe is awesome

lightscribe is the most awesome technology i have witnessed - amazing stuff. professional quality out of the box badsas anyhow, it's rad. on average a full image takes anywhere from 15-25 minutes to burn - the time is well spent - the design package that came with the pack "prints" the design, the package prompts you all sortsa blah blah. it's worth answerin because after all - blah blah reminds you that some bastard over yalls onder and back had to program that blah blah and it said a load of jack that actureally mattered. programmers all over the planet right now are laughing about this that and the other php perl myscript or your script or whatever have you - and props out to for givin me a such an awesome technology as a dual-purpose laser etching through microns of material... i'm sure someone will come along and try to make the whole thing faster, believe me though -buyer beware - the time frame is awesome on this model - between every print a pause - time to reflect on the product... create a lineage of prints or refine a particular ... blah blah blah---

also in the news - walmart serves up a mean salmon! on rare occassions legend tells of excellent fresh salmon steaks flying in from around the globe and landing right in the right place at the right time and with some hickory chips and a half hour cookin slow... you gotta respect their shipping and handling department - they are the masters of transportatio hats off to ya's!

Thursday, March 09, 2006

How to grow THC enzymatically






INVENTION TITLE

Methods and Compositions Relating To Extensible Transgenic Vector Assembler, Pestilence Ridder, Plus Cannabinoid Producer

DESCRIPTION

[Para 1] The present invention relates the compositions and methods for controlling harmful pestilence in toilets and sewage, using modular extensible genetic techniques, and the facilitation of rapid, low-cost, cannabinoid production.

[Para 2] Cannabinoids, traditionally synthesized in Cannabis Sativa, have served as agricultural reagents throughout the world for thousands of years. In light of recent technological advances one skilled in the arts may now synthesize these handy molecules in transgenic vectors such as e. coli and tobacco. This development may enable those skilled in the arts to supply enormous quantities of cannabinoid enriched media to consumers for the purpose of fungicidal, anti-microbial, and insecticidal use.

[Para 3] With regards to the issue of treating filth dispersed deep in underground sewers and inaccessible areas - the invention makes a stark contrast to previous arts. Whereas most chemical reactions must obey the laws of Brownian motion or undergo energetically unfavorable processes such as pumping (USPTO 5,360,556) or heating (USPTO 6,753,536), enzymatic reactions enabled in motile vectors hold a decisive advantage as they can move through a liquid medium more easily. As one skilled in the arts appreciates the possibility of using a motile plant vector such as the sperm of the gingko would allow even greater motility for the vector. In the preferred embodiment of this invention catalysts hosted in transgenic e. coli, transgenic tobacco root hair, and used in modular extensible vectors controlling the synthesis of compounds such as tetrahydrocannabinolic acid (THCA), cannabigerolic acid (CBGA), cannabichromenic acid (CBMA), the associated long term costs of pestilence control may be reduced dramatically - while simultaneously enriching the soil with valuable nutrients for commercial crops. As one skilled in the arts will appreciate - the long term application of the proposed invention will manifest itself in stages - much as any great culture ranging from ancient cheese and yogurt cultures to present day bio-engineered vectors, each application of the invention may, in the spirit of evolution, lead to a unique bio-transformation specifically adapted to its environment. The proposed invention brings to the table a base level of safer transmutation of certain toxic fungi (Llewellyn 1977), (Turner 1981), infectious microbes, (Van Klingeren 1976), (Schmitz 1973), and insect pests, (Quaghebeur, 1981) as well as infectious disease transmitted through insects such as West Nile Virus (McPartland, 1993). The nature of this invention is energetically favorable, easily propagated, and low up-keep in cost making it also ideal for third-world implementation in the pursuit of cleaner, safer land. In cases of emergency the preferred embodiment might also serve as a possible source of the neuroprotectant delta-nine tetrahydrocannabinol (THC) through the application of heat such as sunlight or direct flame. In the event of a terrorist attack of neurotoxins, for instance, one might as a means of last resort set fire to the growth medium to convert THCA to THC - which upon inhaling provides neuroprotection (Hampson 1998) (Van der Stelt 2001) (Mechoulam 2001) (USPTO 6,630,507). Whereas in prior arts Elsohy et al (USPTO 6,730,519) disclosed a method for reduced cost THC production they also rely on traditional abiotic, inorganic, energetically unfavorable means for THC extraction and purification of THC. Moreover their claims depend on natural growth of Cannabis Sativa, a process that may take up to fifteen weeks. Clearly this is not an acceptable waiting period in the case of a terrorist attack. In an alternate embodiment of the invention a serum of raw nutrients, as opposed to raw sewage, were used as the basic medium - in this case using modularized transgenic enzymatic techniques one skilled in the arts might produce several tons of THC in two to three days.

Heading

Description of Operation

[Para 4] As one skilled in the arts may appreciate the variety of vectors able to transform of the initial reagents (TSCSL, TOAP, TCAs, TTAs, TCBMs, TCBAs) into the desired reagents (THC, CBD, CBM) may result in hundreds or thousands of potential scenarios. Consider the heat that is generated in many compost conversion where temperatures may rise above 160 degrees Fahrenheit, in such cases it may be expedient to use an thermophilic vector, particularly for the incubation of the TSCSL, and TOAP. In the preferred embodiment of the invention it should be noted that the TTAs, TCBMs, TCBAs, are used in either a plant or animal vector - since cannabinoids exhibits both anti-microbial and anti-fungal activity it will require a non-microbial and non-fungal host.

[Para 5] In its preferred embodiment begin with a gigantic pile of refuse, that may include fecal matter, untreated sewage water, and decaying animal parts. It may be to the advantage of the user to initiate the enzymatic activity in a more sterile environment with nutrients needed for the synthesis of precursors of cannabinoids to alleviate environmental pressures of the sludge. In such cases as necessary the resulting enzymes and precursor products may be added directly to the filthy sludge or set aside and used as the growth medium for the transgenic cannabinoid synthesis with the resulting cannabinoids added to the filth sludge after their synthesis is completed. See FIGURE 1

[Para 6] Expose the pile of refuse to TSCSLs, TOAPs, and TCs teas - brewed as per the guideline in the literature commonly as anyone skilled in the arts will appreciate - and genetically modified to include promoters operably linked to bioluminescent proteins to help indicate and monitor effectiveness of the treatment. This tea is given from 24 hours to one month as indicated by bioluminescence (Figure 1) to finish blending in with the refuse - or as long as the bioluminescence appears active. (Figure 1. Step: Stilbene-like Synthase). These teas, when mixed with toxic bilge, enzymatically synthesize cannabinoids.

[Para 7] Next a root bed made of TTAs, TCBAs, and or TCBMs. Note the versatility of this invention. Any one of the aforementioned synthases, or indeed all three may be placed atop the pile bilge to create the desired reagents (ie THC, CBA, CBM). Also noteworthy is the elegant closed-loop nature of this system. By initiating the reaction with microbes that are not themselves immune to the final product the system will eventually turn itself off - as the reagent levels rise to higher levels the TSCSLs, TOAPs, and TCs die.

Heading

Description of Operation of Alternate Embodiments

[Para 8] The bucket containing the OAP is loosened atop a pile of crud, that may consist of any decaying or decayed matter, and that must consist of some decaying vegetable matter or living vegetation.

[Para 9] The bucket containing the CAS is loosened atop the pile of crud that previously received OAP treatment.

[Para 10] A blanket of roots from tobacco made of TTAs, TCBAs and or TCBMs are thrown over the crapulence and festering therein may it yield bountifully cannabinoids.

[Para 11] If time is of the essence one may speed up growth times by dispersing units of TEVs around the afflicted region through artificial or assisted means.

[Para 12] If precision in timing is desired it may be convenient to include a bioluminescent protein operably linked a functional promoter to the TEVs similar in methods to (USPTO 6,544,729) and created such as to reflect the activity of the TEVs.

Heading

Overview of Invention

[Para 13] This invention relates to the synthesis of cannabinoids for the purpose of general pestilence riddance in filthy organic and inorganic sludge. Through regulated enzymatic reactions, wherein cannabinoids with known anti-microbial, insecticidal, nematicidal, fungicidal properties and moreover nutritious, and neuroprotective, qualities are used to benefit regions where other commercial chemical reagents would require mechanized dispersion and cleanup. In plain English for those skilled in the arts - the genes involved in the enzymatic formulation of cannabinoids are inserted into foreign vectors thereby reproducing themselves and generating sufficient quantities of cannabinoids to clear the region of pestilence.

[Para 14] The advantages of this system are numerous. Whereas cannabinoid synthesis may not easily take place in Cannabis sativa due to its illegality, this invention is highly preferable. Whereas cannabinoid synthesis using inorganic techniques is not advantageous due to the inefficiency of inorganic and organic laboratory chemistry, this invention is highly preferable. Whereas most chemical synthesis routes for the creation of cannabinoids relate to the creation of extremely pure cannabinoids, this invention merely creates sufficient quantities as needed to rid a region of pestilence, and makes no claims whatsoever as to purity. Whereas the cost of creating cannabinoids synthetically would require large sums of money, as well as recurring costs for reagents, as well as a high degree of expertise and lab equipment, the invention described herein requires a single up-front cost to create the necessary vectors, and thereafter the invention may be distributed and applied to sludge and filth across the world with almost no requirements insofar a priori knowledge.

[Para 15] Using closed-loop modular enzymatic reactions, wherein each phase of catalysis may be halted by another counter reaction, and wherein each phase of catalysis may be easily monitored for effectiveness allows one skilled in the arts to more safely and effectively treat hazardous waste and the plethora of contagions therein. This invention refers to modular, in the sense that along the enzymatic pathway of choice each enzymatic building block is separated into a unique vector, uniquely identifiable by means bioluminescence and uniquely susceptible to a flavor of anti-microbial or anti-fungal such that the enzymatic process of choice may be halted at any given phase of production if desired. Modular may also or rather refer to the system as a whole, in that it should, handled by one skilled in the arts, leave little or no trace of enzymatically active reagent and be a closed-loop system - with the understanding that in nature there exists no such thing as an entirely closed-loop system, however, the preferred embodiment of this invention has in its design constructs a self-destruct or self-neutralizing mechanism for the living reagents. Thus in the preferred embodiment of the invention the catalysis of tetrahydrocannabinolic acid results in the recursive destruction of the initial vectors (Taura 2004).

Heading

Description of Objects

[Para 16] Polyketide Synthesis converts 3 Malonyl CoA plus 1 n-Hexanoyl-CoA to form OSCoA. This conversion may take place inside the muck and sludge, or may take place in a contained area and after the OSCoA.

[Para 17] Stilbene Carboxylate Synthase-Like (STCSL), in the case of Cannabis Sativa a Chalcone Synthase (CHS) that exhibits Stilbene Synthase (STS) activity in vivo and as per note in the literature (Raharjo 2004) there is reason to believe that the sequis used in the preferred embodiment of this invention and refers to any enzyme that generates 5-amylresorcinolic acid (olivetolic acid). While there are several enzymes capable of synthesizing olivetolic acid in the final analysis any enzyme capable of Olivetolic Acid synthesis will is sufficient. In the preferred embodiment the STCSL is inserted into the mitochondrial genome using the protofection technique (Khan 2004). The STCSL should be operably linked to bioluminescent protein to facilitate the monitoring of activity. The vector of the STCSL should also, in the preferred embodiment, have an operably linked In an alternate embodiment of this invention olivetolic acid is synthesized through inorganic techniques and thus added to the filthy sludge as a trigger molecule. In this manner the invention would have a limiting reagent from the offset, restricting the final output of pestilence ridders in such cases wherein limitations might be preferable. In another alternate embodiment of the invention the STCSL is chimeric with GOAP, or a pestilence ridding molecule.

[Para 18] Geranylpyrophosphate Olivetolic Acid Prenylase (GOAP) (Fellermeier 1998) is an integral part of this invention, and converts olivetolic acid into cannabigerolic acid. As one skilled in the art may appreciate any enzyme capable of yielding cannabigerolic acid is sufficient. In the preferred embodiment the GOAP is loaded into the vector in the manner described in Fellermeier’s work. In the preferred embodiment of this invention the GOAP is operably linked to a bioluminescent protein such as GFP or aequorin, and thus its activation is more easily monitored with minimal technical expertise. The GOAP is also operably linked to a promoter capable of up-regulating GOAP and thereby amplifying GOAP production.

[Para 19] Products made from these transgenic vectors should produce THCA, and, in addition, other precursor molecules as well as the necessary enzymes and proteins requisite for the aforementioned production, such as, tetrahydrocannibigerolic acid synthase, cannabigerolic acid synthase (CBGAS), cannabidiolic acid synthase (CBDAS), cannabichromenic acid synthase (CBRMAS), tetrahydrocannibinolic acid (THCA), olivetolic acid, polyketide synthase, and cannabigerolic acid synthase. Also disclosed is the unique and novel application of the TTAs in the function of a compost toilet additive and for the low-impact, sustainable, macrobiotic control of pests including Alabama argillacea (Riley 1885), Pieris brassicae (Beling 1932), Melolontha melolontha (Mateeva 1995), and Aphelenchoides composticola, (Grewal 1989).

Heading

Enzyme Reference Table

[Para 20] Table 1

Enzyme

Reagents

Product

Time

Temp

Vector

Key References

Polyketide / STCSL / CoAs

3 MalonylCo-A & 1 n-Hexanoyl-CoA

OSCoA

OSCoA

Olivetolic Acid

1-24 hrs

25-35 C

E. Coli M15

Raharjo, 2004

Prenylase

Olivetolic Acid + GPP

Cannabigerolic Acid

1-24 hrs

25-35 C

E. Coli M15

Fellermeier, 1998

CBCAs

Cannabigerolic Acid

Cannabidiolic Acid

24-48 hrs

25-35 C

Tobacco Root Hairs

Morimoto, 1999

CBDAs

Cannabigerolic Acid

Cannabichromenic Acid

24-48 hrs

25-35 C

Tobacco Root Hairs

Morimoto, 1999

THCAs

Cannabigerolic Acid

Tetrahydrocannabinolic Acid

24-48 hrs

25-35 C

Tobacco Root Hairs

Taura, 1995 & Sirikantaramas, 2004

Definition List 1

Term

Definition

Transgenic Stilbene-carboxylate synthase-like enzyme (TSCSL) (see Fellermeier 1998)

Any enzymatic reaction or nano-bot that yields Olivetolic Acid. The trigger mechanism. In alternate embodiments of this invention TSCSL is linked operably to a bioluminescent and equipped with a unique “off switch.”

Transgenic Geranylpyrophosphate Prenylase (TOAP) (see Fellermeier 1998)

Any enzymatic reaction or nano-bot that yields Cannabigerol. In an alternate embodiment TOAP is linked operably to a bioluminescent and equipped with a unique “off switch”.

Transgenic Cannabigerolic Acid Synthase (TCAs) (See Raharjo 2002)

Any enzymatic reaction or nano-bot that synthesizes Cannabigerolic Acid. In alternate embodiments of this invention TCAs is linked operably to a bioluminescent and equipped with a unique “off switch.”

Transgenic Cannabidiolic Acid Synthase (TCBAs) (see Taura F. 1996)

Any enzymatic reaction or nano-bot that synthesizes Cannabidiolic Acid. In the preferred embodiment of this invention TCBAs is linked operably to a bioluminescent and equipped with a unique “off switch.”

Transgenic Tetrahydrocannabinolic Acid Synthase (TTAs)” (see Taura 2004)

Any enzymatic reaction or nano-bot that synthesizes THCA. In an alternate embodiment of this invention TTAs is linked operably to a bioluminescent and equipped with a unique “off switch.”

Transgenic Cannabichromene Synthase (TCBMs)

Any enzymatic reaction or nano-bot that synthesizes Cannabichromenic Acid. In an alternate embodiment of this invention TCBMs is linked operably to a bioluminescent and equipped with a unique “off switch.”

Genetic “Off switch”

Any of several dozen enzymes with known lethality targeting specifically the aforementioned transgenic vectors - each with its own unique off switch.

waste water, raw sewage, bilge water, manure, compost, toxic sludge, filth, festering rot, crud, crude, crapulence, rubbage, and debris

Used interchangeably in reference to any medium that may need or accept pestilence management.

Pestilence management

Refers to the control - be it through repellence, extermination, or slowing of growth rate, of any or several of the following organisms Alabama argillacea (Riley 1885), Pieris brassicae (Beling 1932), Melolontha melolontha (Mateeva 1995), and Aphelenchoides composticola, (Grewal 1989), potato beetle (Leptinotarsa decemlineata) (Stratii 1976), mosquito larvae (Anopheles and Culex species)(Jalees et al. 1993), Chilo partellus, (a lepidopteran borer)(Bajpai and Sharma, 1992), Tetranychus urticae (Fenili and Pegazzano, 1974). Japanese beetles (Metzger and Grant, 1932), Heterodera cajani (Mojumder et al. 1989), Ustilago species (Misra and Dixit 1979, Singh and Pathak 1984), Neovossia indica (Gupta and Singh 1983), Curvularia (Upandhyaya and Gupta, 1989), Colletotrichum truncatum (Kaushal and Paul, 1989), Aspergillus, Penicillium, Cladosporium, Drechslera, Fusarium, Cephalosporium, Rhizopus, Mucor and Curvularia (Pandey, 1982), gram (+) S. aureus, Bacillus megaterium (Veliky and Genest 1972), gram (+) Corynebacterium species and gram (-) Pseudomonas and Agrobacterium species (Bel’tyukova 1962), Trypanosoma brucei (Nok et al., 1994), Phomopsis ganjae (Charles and Jenkins 1914, McPartland 1983), Arctia caja (Rothschild et al., 1977) or any other known or unknown organism with undesirable traits.

Transgenically enhanced vector (TEV)

Any vector, its parental lineage or its offspring that has been modified by the use of modern or Mendelian genetic techniques to produce a compound.

operably linked

Refers to a juxtaposition wherein the components so described are in a relationship permitting them to function in their intended manner. A control sequence "operably linked" to a coding sequence is ligated in such a way that expression of the coding sequence is achieved under conditions compatible with the control sequences.

Floatation system

In the preferred embodiment floating systems with roots embedded are used to suspend the transgenic roots as they convert cannabigerolic acid into cannabinoids.

Bioluminescent protein

Refers to a protein capable of causing the emission of light through the catalysis of a chemical reaction. The term includes proteins that catalyze bioluminescent or chemiluminescent reactions, such as those causing the oxidation of luciferins. The term "bioluminescent protein" includes not only bioluminescent proteins that occur naturally, but also mutants that exhibit altered spectral or physical properties.

Transformed

Refers to a cell into which (or into an ancestor of which) has been introduced, by means of recombinant nucleic acid techniques, a heterologous nucleic acid molecule.

Transgenic

Describes an organism or cell line that includes exogenous genetic material within all of its cells. The term includes any organism whose genome has been altered by in vivo or in vitro manipulation of the early embryo or fertilized egg or by any transgenic technology to induce a specific gene knockout.

Transgene

Any piece of DNA which is inserted by artifice into a cell, and becomes part of the genome of the organism (i.e., either stably integrated or as a stable extrachromosomal element) which develops from that cell. Such a transgene may include a gene which is partly or entirely heterologous (i.e., foreign) to the transgenic organism, or may represent a gene homologous to an endogenous gene of the organism. Included within this definition is a transgene created by the providing of an RNA sequence that is transcribed into DNA and then incorporated into the genome. The transgenes of the invention include DNA sequences that encode the fluorescent or bioluminescent protein that may be expressed in a transgenic non-human animal, the genes required for the synthesis of cannabinoids, and any additional genetic information necessary for the greater control of the invention.

The following terms are used to describe the sequence relationships between two or more polynucleotides: "reference sequence", "comparison window", "sequence identity", "percentage identical to a sequence", and "substantial identity"

A "reference sequence" is a defined sequence used as a basis for a sequence comparison; a reference sequence may be a subset of a larger sequence, for example, as a segment of a full-length cDNA or gene sequence, or may comprise a complete cDNA or gene sequence. Generally, a reference sequence is at least 20 nucleotides in length, frequently at least 25 nucleotides in length, and often at least 50 nucleotides in length. Since two polynucleotides may each (1) comprise a sequence (i.e., a portion of the complete polynucleotide sequence) that is similar between the two polynucleotides, and (2) may further comprise a sequence that is divergent between the two polynucleotides, sequence comparisons between two (or more) polynucleotides are typically performed by comparing sequences of the two polynucleotides over a "comparison window" to identify and compare local regions of sequence similarity. A "comparison window", as used herein, refers to a conceptual segment of at least 20 contiguous nucleotide positions wherein a polynucleotide sequence may be compared to a reference sequence of at least 20 contiguous nucleotides and wherein the portion of the polynucleotide sequence in the comparison window may comprise additions or deletions (i.e., gaps) of 20 percent or less as compared to the reference sequence (which does not comprise additions or deletions) for optimal alignment of the two sequences. Optimal alignment of sequences for aligning a comparison window may be conducted by the local homology algorithm of Smith and Waterman (1981) Adv. Appl. Math. 2:482, by the homology alignment algorithm of Needleman and Wunsch (1970) J. Mol. Biol. 48:443, by the search for similarity method of Pearson and Lipman (1988) Proc. Natl. Acad. Sci. (U.S.A.) 85:2444, by computerized implementations of these algorithms (GAP, BESTFIT, FASTA, and TFASTA in the Wisconsin Genetics Software Package Release 7.0, Genetics Computer Group, 575 Science Dr., Madison, Wis.), or by inspection, and the best alignment (i.e., resulting in the highest percentage of homology over the comparison window) generated by the various methods is selected. The term "sequence identity" means that two polynucleotide sequences are identical (i.e., on a nucleotide-by-nucleotide basis) over the window of comparison. The term "percentage identical to a sequence" is calculated by comparing two optimally aligned sequences over the window of comparison, determining the number of positions at which the identical nucleic acid base (e.g., A, T, C, G, U, or I) occurs in both sequences to yield the number of matched positions, dividing the number of matched positions by the total number of positions in the window of comparison (i.e., the window size), and multiplying the result by 100 to yield the percentage of sequence identity. The terms "substantial identity" as used herein denotes a characteristic of a polynucleotide sequence, wherein the polynucleotide comprises a sequence that has at least 30 percent sequence identity, preferably at least 50 to 60 percent sequence identity, more usually at least 60 percent sequence identity as compared to a reference sequence over a comparison window of at least 20 nucleotide positions, frequently over a window of at least 25-50 nucleotides, wherein the percentage of sequence identity is calculated by comparing the reference sequence to the polynucleotide sequence which may include deletions or additions which total 20 percent or less of the reference sequence over the window of comparison. As applied to polypeptides, the term "substantial identity" means that two peptide sequences, when optimally aligned, such as by the programs GAP or BESTFIT using default gap weights, share at least 30 percent sequence identity, preferably at least 40 percent sequence identity, more preferably at least 50 percent sequence identity, and most preferably at least 60 percent sequence identity. Preferably, residue positions which are not identical differ by conservative amino acid substitutions. Conservative amino acid substitutions refer to the interchangeability of residues having similar side chains. For example, a group of amino acids having aliphatic side chains is glycine, alanine, valine, leucine, and isoleucine; a group of amino acids having aliphatic-hydroxyl side chains is serine and threonine; a group of amino acids having amide-containing side chains is asparagine and glutamine; a group of amino acids having aromatic side chains is phenylalanine, tyrosine, and tryptophan; a group of amino acids having basic side chains is lysine, arginine, and histidine; and a group of amino acids having sulfur-containing side chains is cysteine and methionine. Preferred conservative amino acids substitution groups are: valine-leucine-isoleucine, phenylalanine-tyrosine, lysine-arginine, alanine-valine, glutamic-aspartic, and asparagine-glutamine.

Caveat

Since the list of technical and scientific terms cannot be all encompassing, any undefined terms shall be construed to have the same meaning as is commonly understood by one of skill in the art to which this invention belongs. Furthermore, the singular forms "a", "an" and "the" include plural referents unless the context clearly dictates otherwise. For example, reference to a "restriction enzyme" or a "high fidelity enzyme" may include mixtures of such enzymes and any other enzymes fitting the stated criteria, or reference to the method includes reference to one or more methods for obtaining cDNA sequences which will be known to those skilled in the art or will become known to them upon reading this specification.

Heading

USPTO References

[Para 21] Table 2

Author

Title

USPTO #

Keyword

Date

Grobler, Marius ; et al.

Sewage sludge treatment

20050175516

Compost

NA

Liang

Shooting mechanism of an anti-violence gun

6,615,815

Anti-violence

September 9, 2003

Becker , et al.

Method and arrangement of equipment for the protection of buildings and people from acts of violence

5,692,446

Anti-violence

December 2, 1997

Sun

Apparatus for preventing criminal's escape or violence

4,811,775

Anti-violence

March 14, 1989

Peterson, et al.

SPANN: Sequence processing artificial neural network

5,067,095

Modular Vector

November 19, 1991

Case, et al.

Thin membrane sensor with biochemical switch

5,328,847

Modular switch

July 12, 1994

Humphreys, et al.

Apparatus for neutralizing chemical and biological threats

6,753,536

Wastewater cleaning apparatus

June 22, 2004

Ball, et al.

Method of feeding wastewater effluent to filter bed through parallel conduits

5,360,556

Wastewater cleaning apparatus

November 1, 1994

Hampson, et al.

Cannabinoids as antioxidants and neuroprotectants

6,630,507

Cannabis Neuroprotectant

October 7, 2003

Elsohly, et al.

Method of preparing delta-9-tetrahydrocannabinol

6,730,519

THC synthesis

December 4, 2001

Growcock, et al.

Vermiculture compositions

6,838,082

compost biolumin

January 4, 2005

Sayler; Gary S.

Bioluminescent biosensor device

6,544,729

Bioluminbiosensor device

April 8, 2003

Croteau , et al.

Isolation and bacterial expression of a sesquiterpene synthase cDNA clone from peppermint (mentha x piperita, L.) that produces the aphid alarm pheromone (E)-.beta.-farnesene

6,258,602

cannabis insecticide

July 10, 2001

Goodwin, Neil John ; et al

Production of delta 9 tetrahydrocannabinol

20050171361

THC synthesis

August 4, 2005

Martin, Billy R ; et al.

Cannabinoids

20050165259

Cannabinoids

July 28, 2005

Moore, Bob M. II ; et al.

Cannabinoid derivatives, methods of making, and use thereof

20040242593

THC synthesis

December 2, 2004

Chowdhury, Dipak K. ; et al.

Tetrahydrocannabinol compositions and methods of manufacture and use thereof

20040229939

THC manufacture & use

November 18, 2004

Webster , et al.

Cannabinoid extraction method

6,403,126

Cannabinoid extraction

June 11, 2002

McKinney

Method and apparatus for processing herbaceous plant materials including the plant cannabis

4,279,824

THC extraction

July 21, 1981

Heading

References from the literature:

[Para 22] Key References

(1) Abe I, Watanabe T, Noguchi H. Enzymatic formation of long-chain polyketide pyrones by plant type III polyketide synthases. Phytochemistry. 2004 Sep;65(17):2447-53.

(2) Abrol B. K. and I. C. Chopra, 1963. Development of indigenous vegetable insecticides and insect repellents. Bulletin Jamu Regional Res. Lab 1:156. 1963.

(3) Bajpai N. K. and V. K. Sharma. Possible use of hemp (Cannabis sativa L.) weeds in integrated control. Indian Farmers’ Digest 25(12):32, 38, 1992

(4) Beling I.. Schädlingsbekämpfung im 18. Jarhhundert. Anz. Schädlingbekämpfung 8(6):66-69., 1932.

(5) Business Alliance for Commerce in Hemp,"Hemp: Friend to People and Ecology" Los Angeles, CA, April 1994

(6) Cekmecelioglu D, Demirci A, Graves RE., Feedstock optimization of in-vessel food waste composting systems for inactivation of pathogenic microorganisms., J Food Prot. 2005 Mar;68(3):589-96.

(7) Chopra R.N., R. L. Badhwar and S. L. Nayar, 1941. Insecticidal and piscicidal plants of India. J. Bombay Nat. Hist. Soc. 42:854-902.

(8) Dahiya M.S. and G. C. Jain, 1977. Inhibitory effects of cannabidiol and tetrahydrocannabinol against some soil inhabiting fungi. Indian Drugs 14(4):76-79.

(9) Deportes I, Benoit-Guyod JL, Zmirou D, Bouvier MC., Microbial disinfection capacity of municipal solid waste (MSW) composting., J Appl Microbiol. 1998 Aug;85(2):238-46.

(10) Eckermann C, Schroder G, Eckermann S, Strack D, Schmidt J, Schneider B, Schroder J.Stilbenecarboxylate biosynthesis: a new function in the family of chalcone synthase-related proteins.Phytochemistry. 2003 Feb;62(3):271-86.

(11) Eisenreich, W., Schwarz, M., Cartayrade, A., Arigoni, D., Zenk, M.H. & Bacher, A. (1998) The deoxyxylulose phosphate pathway of terpenoid biosynthesis in plants and microorganisms. Chem. Biol. 5, R221±R233.

(12) Fellermeier M, Eisenreich W, Bacher A, Zenk MH., Biosynthesis of cannabinoids. Incorporation experiments with (13)C-labeled glucoses. Eur J Biochem. 2001 Mar;268(6):1596-604.

(13) Ferenczy L. Antibacterial substances in seeds. Nature 178:639-640., 1956.

(14) Ferenczy L., L. Gracza and I. Jakobey. An antibacterial preparatum from hemp (Cannabis sativa). Naturwissenschaften 45:188., 1958.

(15) Ferrer JL, Jez JM, Bowman ME, Dixon RA, Noel JP., Structure of chalcone synthase and the molecular basis of plant polyketide biosynthesis. Nat Struct Biol. 1999 Aug;6(8):775-84. Bioresour Technol. 2001 Dec;80(3):217-25.

(16) Gal I. E., O. Vajda and I. Bekes. A kannabidiolsav néhány tulaj-donságának vizsgálata élelmiszertartósítási szempontból. Elelmiszervizsgalati Közlemenyek 4:208-216.1969.

(17) Grainge M. and S. Ahmed. Handbook of Plants with Pest-Control Properties. John Wiley and Sons, NY. 470 pp., 1988.

(18) Grewal P. S. Effects of leaf-matter incorporation on Aphelenchoides composticola (Nematoda), mycofloral composition, mushroom compost quality and yield of Agaricus bisporus. Annals Applied Biology 115:299-312., 1989.

(19) Gupta R. P. and A. Singh. Effect of certain plant extracts and chemicals on teliospore germination of Neovossia indica. Indian J. Mycology and Plant Pathology 13(1):116-117. 1983.

(20) Hampson AJ, Grimaldi M, Axelrod J, Wink D. Cannabidiol and (-)Delta9-tetrahydrocannabinol are neuroprotective antioxidants. Proc Natl Acad Sci USA 1998 Jul 7;95(14):8268-73

(21) Hassen A, Belguith K, Jedidi N, Cherif A, Cherif M, Boudabous A., Microbial characterization during composting of municipal solid waste.

(22) Jager E, Ruden H, Zeschmar-Lahl B., [Composting facilities. 1. Microbiological quality of compost with special regard to disposable diapers], Zentralbl Hyg Umweltmed. 1994 Oct;196(3):245-57. German.

(23) Jalees S., S. K. Sharma, S. J. Rahman and T. Verghese, 1993. Evaluation of insecticidal properties of an indigenous plant, Cannabis sativa L., against mosquito larvae under laboratory conditions. J. Entomol. Res. 17:117-120. 1993.

(24) Jenkins, Phil, "Field of Opportunity" Canadian Geographic, 03/19/99

(25) Kane VV, Razdan RK. Constituents of hashish. A novel reaction of olivetol with citral in the presence of pyridine. Total synthesis of dl-cannabicyclol and dl-cannabichromene. J Am Chem Soc. 1968 Nov 6;90(23):6551-3.

(26) Kashyap N. P., R. M. Bhagat, D. C. Sharma and S. M. Suri, 1992. Efficacy of some useful plant leaves for the control of potato tuber moth, Phthorimaea operculella Zell. in stores. J. Entomological Research 16:223-227. 1992.

(27) Khan SM, Bennett JP Jr., Development of mitochondrial gene replacement therapy., J Bioenerg Biomembr. 2004 Aug;36(4):387-93. Review.

(28) Kir’yanova E. S. and E. L. Krall. Plant-Parasitic Nematodes and their Control, Vol. II. Academy of Sciences of the USSR, Nauka Publishers, Leningrad. 1971.

(29) Klingeren B. van and M. T. Ham. Antibacterial activity of delta-9-tetrahydrocannabinol and cannabidiol. Antonie van Leeuwenhoek 42:9-12., 1976.

(30) Kok C.J., G. C. M. Coenen, and A. de Heij, 1994. The effect of fibre hemp (Cannabis sativa L.) on selected soil-borne pathogens. J. International Hemp Association 1(1):6-9.

(31) Kurilov V. I. and N. S. Kakhta. [More about hemp and the Colorado beetle.] Zashchita Rastenii 1977 (7):63. 1977.

(32) Lenehan NA, DeRouchey JM, Marston TT, Marchin GL. Concentrations of fecal bacteria and nutrients in soil surrounding round-bale feeding sites., J Anim Sci. 2005 Jul;83(7):1673-9.

(33) Llewellyn GC, O'Rear CE., Examination of fungal growth and aflatoxin production on marihuana., Mycopathologia. 1977 Dec 16;62(2):109-12.

(34) Loewe S., 1946. Studies on the pharmacology and acute toxicity of compounds with marihuana activity. J. Pharmacology and Expermental Therapeutics 88:154-164.

(35) Mackiewicz S., 1962. The effect of hemp on the density of the potato beetle and the bean aphid. Biul. Ochrona Roslin Inst. 16:101-131.

(36) Mateeva A. Use of unfreindly plants against root knot nematodes. Acta Horticulturae 382 (Feb):178-182. 1995.

(37) McPartland J. M., Fungal pathogens of Cannabis sativa in central Illinois. Phytopathology 73:797., 1983,

(38) McPartland J. M.. Pathogenicity of Phomopsis ganjae on Cannabis sativa and the fungistatic effect of cannabinoids produced by the host. Mycopathologia 87:149-153., 1984

(39) McPartland, John M., Cannabis as repellent and pesticide, Journal of the International Hemp Association 4(2): 87-92, 1997

(40) Mechoulam R, Hanu L. The cannabinoids: an overview. Therapeutic implications in vomiting and nausea after cancer chemotherapy, in appetite promotion, in multiple sclerosis and in neuroprotection. Pain Res Manag 2001 Summer;6(2): 67-73.

(41) Mechoulam R, Spatz M, Shohami E. Endocannabinoids and neuroprotection. Sci STKE Apr 23;(129):RE5. 2002.

(42) Metzger F. W. and D. H. Grant. Repellency to the Japanese beetle of extracts made from plants immune to attack. USDA Technical Bulletin no. 299. 21 pp., 1932.

(43) Misra S. B. and S. N. Dixit. Antifungal activity of leaf extracts of some higher plants. Acta Botanica Indica 7:147-150, 1979.

(44) Mojumder V., S. D. Mishra, M. M. Haque and B. K. Goswami. Nematicidal efficacy of some wild plants against pigeon pea cyst nematode, Heterodera cajani. Int. Nematol. Network Newsletter 6(2):21-24, 1989.

(45) Nok A. J., S. Ibrahim, S. Arowosafe, et al.. The trypanocidal effect of Cannabis sativa constituents in experimental animal try-panosomiasis. Veterinary and Human Toxicology 36:522-524 , 1994.

(46) S. Morimoto, F. Taura, Y. Shoyama, Biosynthesis of cannabinoids in Cannabis sativa L, Curr. Top. Phytochem. 2 (1999) 103–113.

(47) Oku,T. and Katsura,Y. “Sequence analysis encoding alpha-helix-turn-alpha-helix motif of HrpX in plant pathogenic Xanthomonas”, Unpublished

(48) Pandey K. N.. Antifungal activity of some medicinal plants on stored seeds of Eleusine coracana. J. Indian Phytopathology 35:499-501.1982.

(49) Pandey J. and S. S. Mishra. Effects of Cannabis sativa L. on yield of rabi maize (Zea mays L.). in Abstracts of papers, Annual conference of Indian Society of Weed Science. Bihar, India. 1982.

(50) Prakash A., I. C. Pasalu and K. C. Mathur, 1982. Evaluation of plant products as paddy grain protectants in storage. International J. Entomology 1:75-77.

(51) Prakash A., J. Rao and I. C. Pasalu, 1987. Studies on stored grain pests of rice and methods of minimising losses caused by them. Final Project Report (RPF-III) Ent-6/CRRI/ICAR (India). 33 pp.

(52) Quaghebeur K, Coosemans J, Toppet S, Compernolle F., Cannabiorci- and 8-chlorocannabiorcichromenic acid as fungal antagonists from Cylindrocarpon olidum., Phytochemistry. 1994 Sep;37(1):159-61.

(53) Radosevic A., M. Kupinic and L. Grlic. Antibiotic activity of various types of Cannabis resin. Nature 195:1007-1009. 1962.

(54) Raharjo, Tri J; Chang, Wen-Te; Verberne, Marianne C; Peltenburg-Looman, Anja M G; Linthorst, Huub J M; Verpoorte, Robert,Cloning and over-expression of a cDNA encoding a polyketide synthase from Cannabis sativa, Plant Physiology and Biochemistry - Paris, 42 (4), 291-298, 2004.

(55) Riley C. V. and L. O. Howard. Hemp as a protection against weevils. Insect Life (USDA) 4: 223 1892.

(56) Rothschild M., M. R. Rowan and J. W. Fairbairn. Storage of cannabinoids by Arctia caja and Zonocerus elegans fed on chemically distinct strains of Cannabis sativa. Nature 266:650-651. 1977.

(57) Schmitz JA, Olson LD., Duration of viability and the growth and expiration rates of group E streptococci in soil., Appl Microbiol. 1973 Feb;25(2):180-3.

(58) Shoyama, Y., Hirano, H., and Nishioka, I. (1978) J. Labelled Compd. Radiopharm. 14, 835-842

(59) Sirikantaramas S, Morimoto S, Shoyama Y, Ishikawa Y, Wada Y, Shoyama Y, Taura F., The gene controlling marijuana psychoactivity: molecular cloning and heterologous expression of Delta1-tetrahydrocannabinolic acid synthase from Cannabis sativa L., J Biol Chem. 2004 Sep 17;279(38):39767-74. Epub 2004 Jun 9.

(60) Stratii Y. I.. Hemp and the Colorado beetle. Zashchita Rasteniî 5:61., 1976.

(61) Taura, F., Morimoto, S., Shoyama, Y., and Mechoulam, R. (1995) J. Am. Chem Soc. 117, 9766–9767

(62) Taura, F., Morimoto, S., and Shoyama, Y. (1996) J. Biol. Chem. 271, 17411–17416

(63) F. Taura, S. Morimoto and Y. Shoyama, Biosynthesis of marihuana compounds - Purification and characterization of biosynthetic enzymes. Current Topic in Plant Biology, Vol. 2 p63-73 (2000), 2000..

(64) Turner CE, Elsohly MA., Biological activity of cannabichromene, its homologs and isomers., J Clin Pharmacol. 1981 Aug-Sep;21(8-9 Suppl):283S-291S.

(65) Van der Stelt M, Veldhuis WB, Bar PR, Veldink GA, Vliegentharet JF, Nicolay K. Neuroprotection by Delta9-tetrahydrocannabinol, the main active compound in marijuana, against ouabain-induced in vivo excitotoxicity. J Neurosci 2001 Sep 1;21(17): 6475-

(66) Van Haute, E., Joos, H., Maes, M., Warren, G., Van Montagu, M., and Schell, J. EMBO J. 2, 411–417, 1983.

(67) Van Klingeren B, Ten Ham M. Antibacterial activity of delta9-tetrahydrocannabinol and cannabidiol., Antonie Van Leeuwenhoek; 42(1-2):9-12 1976.

(68) Veliky I. A. and R. K. Latte. Antimicrobial activity of cultured plant cells and tissues. Lloydia 37:611-620., 1974.

(69) Vijai P., I. Jalali and R. D. Parashar. Suppression of bacterial soft rot of potato by common weed extracts. J. Indian Potato Association 20:206-209, 1993.

(70) White, F. F., and Nester, E. W. J. Bacteriol. 141, 1134–1141, 1980.

(71) T. Yamaguchi, F. Kurosaki, D.-Y. Suh, U. Sankawa, M. Nishioka, T. Akiyama, M. Shibuya, Y. Ebizuka, Cross-reaction of chalcone synthase and stilbene synthase overexpressed in Escherichia coli, FEBS Lett. 460 457–461, 1999.

(72) Zelepukha S. I., 1960. The third conference on the problem of phytoncides. J. Mikrobiol, Kiev 22(1):68-71.

What is claimed is:

[Claim 1] Enzymatic reactions initiated in transgenic vector organisms generate cannabinoids - fungicidal, anti-microbial, and insecticidal in nature.

[Claim 2] Transgenic vector organisms represent an extensible substrate and may be retrofitted with additional transgenes to facilitate production insofar as timing and precision cannabinoid production is concerned.

[Claim 3] Transgenic vector organisms may be retrofitted with additional transgenes to facilitate a closed-loop system – thereby lessening the overall ecological impact of rampant transgenic DNA.

ABSTRACT

[Para 23] Regions of standing wastewater harboring high concentrations of unprocessed, unfiltered rubbage and manure can be natural sites for disease. The need for low-impact, low-maintenance composting solutions is needed to address city sewers and streets around the world that routinely overflow with toxic bilge. Controlling pests in such regions may often require the use of manufactured chemicals - created along costly and inefficient energy gradients (USPTO 5,227,537). Many of these chemical treatments present long-term hazards to the environment in the forms of run-off contamination, and build-up. Once introduced into a system these non-biodegradable inorganic compounds may not easily be eradicated. Although these methods may be suitable for certain bilge water, especially in treatment facilities where build-up and run-off are not concerns, they do not address the needs of farmers dealing with compost piles, nor sewage water running rampant through the streets of cities that have been obliterated by tsunamis, hurricanes, or tornadoes - wherein there may be an immediate need for rapid decomposition and pestilence ridding. Nor do these prior arts address the need for low impact conversion and or transmutation of toxins and pestilence, nor do these methods establish within the bilge an ecological breeding ground wherein one skilled in the arts might hope to use the nutrient rich, albeit highly toxic, solution for the establishment of biological byproduct. On the other hand, allowing the degradation of the toxic bilge to take place naturally may not be a viable option - as the aforementioned pestilence may soon make a bid to use the nutrient source as a home. In the proposed invention one skilled in the arts would safely apply numerous vectors to convert the bilge into valuable natural resources while simultaneously defending the region from harmful pestilence both through the creation of anti-microbial substances and through direct competition for resources - in much the same way that acidophilus in yogurt out-competes other microbes.

DRAWINGS