USH110H - Tracking of air mass movement - Google Patents
Tracking of air mass movement Download PDFInfo
- Publication number
- USH110H USH110H US06/799,531 US79953185A USH110H US H110 H USH110 H US H110H US 79953185 A US79953185 A US 79953185A US H110 H USH110 H US H110H
- Authority
- US
- United States
- Prior art keywords
- air
- air mass
- medium
- citrate
- movement
- Prior art date
- Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
- Abandoned
Links
- 241000193830 Bacillus <bacterium> Species 0.000 claims abstract description 15
- KRKNYBCHXYNGOX-UHFFFAOYSA-K Citrate Chemical compound [O-]C(=O)CC(O)(CC([O-])=O)C([O-])=O KRKNYBCHXYNGOX-UHFFFAOYSA-K 0.000 claims abstract description 13
- 239000000700 radioactive tracer Substances 0.000 claims abstract description 9
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 claims abstract description 8
- 229910052799 carbon Inorganic materials 0.000 claims abstract description 8
- 239000003570 air Substances 0.000 claims description 21
- 238000000034 method Methods 0.000 claims description 15
- 239000002609 medium Substances 0.000 claims description 14
- 238000012544 monitoring process Methods 0.000 claims description 5
- 239000001963 growth medium Substances 0.000 claims description 4
- 239000012080 ambient air Substances 0.000 claims description 3
- 241000894006 Bacteria Species 0.000 abstract description 13
- 230000001580 bacterial effect Effects 0.000 abstract 1
- 239000002245 particle Substances 0.000 description 7
- CSNNHWWHGAXBCP-UHFFFAOYSA-L Magnesium sulfate Chemical compound [Mg+2].[O-][S+2]([O-])([O-])[O-] CSNNHWWHGAXBCP-UHFFFAOYSA-L 0.000 description 4
- 239000000463 material Substances 0.000 description 4
- 230000002285 radioactive effect Effects 0.000 description 4
- 229920001817 Agar Polymers 0.000 description 3
- 241000283690 Bos taurus Species 0.000 description 3
- KRHYYFGTRYWZRS-UHFFFAOYSA-M Fluoride anion Chemical compound [F-] KRHYYFGTRYWZRS-UHFFFAOYSA-M 0.000 description 3
- 239000008272 agar Substances 0.000 description 3
- 230000005180 public health Effects 0.000 description 3
- 238000005070 sampling Methods 0.000 description 3
- 239000001509 sodium citrate Substances 0.000 description 3
- NLJMYIDDQXHKNR-UHFFFAOYSA-K sodium citrate Chemical compound O.O.[Na+].[Na+].[Na+].[O-]C(=O)CC(O)(CC([O-])=O)C([O-])=O NLJMYIDDQXHKNR-UHFFFAOYSA-K 0.000 description 3
- 231100000331 toxic Toxicity 0.000 description 3
- 230000002588 toxic effect Effects 0.000 description 3
- IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 description 2
- 241001465754 Metazoa Species 0.000 description 2
- FAPWRFPIFSIZLT-UHFFFAOYSA-M Sodium chloride Chemical compound [Na+].[Cl-] FAPWRFPIFSIZLT-UHFFFAOYSA-M 0.000 description 2
- XAGFODPZIPBFFR-UHFFFAOYSA-N aluminium Chemical compound [Al] XAGFODPZIPBFFR-UHFFFAOYSA-N 0.000 description 2
- 229910052782 aluminium Inorganic materials 0.000 description 2
- 238000012258 culturing Methods 0.000 description 2
- 230000036541 health Effects 0.000 description 2
- 239000002917 insecticide Substances 0.000 description 2
- 229910052943 magnesium sulfate Inorganic materials 0.000 description 2
- 235000019341 magnesium sulphate Nutrition 0.000 description 2
- LWIHDJKSTIGBAC-UHFFFAOYSA-K potassium phosphate Substances [K+].[K+].[K+].[O-]P([O-])([O-])=O LWIHDJKSTIGBAC-UHFFFAOYSA-K 0.000 description 2
- UQMZPFKLYHOJDL-UHFFFAOYSA-N zinc;cadmium(2+);disulfide Chemical compound [S-2].[S-2].[Zn+2].[Cd+2] UQMZPFKLYHOJDL-UHFFFAOYSA-N 0.000 description 2
- 241000256118 Aedes aegypti Species 0.000 description 1
- 241000255925 Diptera Species 0.000 description 1
- 241000233866 Fungi Species 0.000 description 1
- 239000005083 Zinc sulfide Substances 0.000 description 1
- 238000003916 acid precipitation Methods 0.000 description 1
- 230000002378 acidificating effect Effects 0.000 description 1
- 239000000443 aerosol Substances 0.000 description 1
- 238000003915 air pollution Methods 0.000 description 1
- LFVGISIMTYGQHF-UHFFFAOYSA-N ammonium dihydrogen phosphate Chemical compound [NH4+].OP(O)([O-])=O LFVGISIMTYGQHF-UHFFFAOYSA-N 0.000 description 1
- 229910000387 ammonium dihydrogen phosphate Inorganic materials 0.000 description 1
- 150000003863 ammonium salts Chemical class 0.000 description 1
- NUHCTOLBWMJMLX-UHFFFAOYSA-N bromothymol blue Chemical compound BrC1=C(O)C(C(C)C)=CC(C2(C3=CC=CC=C3S(=O)(=O)O2)C=2C(=C(Br)C(O)=C(C(C)C)C=2)C)=C1C NUHCTOLBWMJMLX-UHFFFAOYSA-N 0.000 description 1
- 229910052793 cadmium Inorganic materials 0.000 description 1
- BDOSMKKIYDKNTQ-UHFFFAOYSA-N cadmium atom Chemical compound [Cd] BDOSMKKIYDKNTQ-UHFFFAOYSA-N 0.000 description 1
- 238000005119 centrifugation Methods 0.000 description 1
- 238000007796 conventional method Methods 0.000 description 1
- 230000034994 death Effects 0.000 description 1
- 231100000517 death Toxicity 0.000 description 1
- ZPWVASYFFYYZEW-UHFFFAOYSA-L dipotassium hydrogen phosphate Chemical compound [K+].[K+].OP([O-])([O-])=O ZPWVASYFFYYZEW-UHFFFAOYSA-L 0.000 description 1
- 229910000396 dipotassium phosphate Inorganic materials 0.000 description 1
- 235000019797 dipotassium phosphate Nutrition 0.000 description 1
- 239000012153 distilled water Substances 0.000 description 1
- 238000005367 electrostatic precipitation Methods 0.000 description 1
- 230000002255 enzymatic effect Effects 0.000 description 1
- 238000011156 evaluation Methods 0.000 description 1
- 238000001914 filtration Methods 0.000 description 1
- 238000009472 formulation Methods 0.000 description 1
- BAUYGSIQEAFULO-UHFFFAOYSA-L iron(2+) sulfate (anhydrous) Chemical compound [Fe+2].[O-]S([O-])(=O)=O BAUYGSIQEAFULO-UHFFFAOYSA-L 0.000 description 1
- 229910000359 iron(II) sulfate Inorganic materials 0.000 description 1
- 239000007788 liquid Substances 0.000 description 1
- SQQMAOCOWKFBNP-UHFFFAOYSA-L manganese(II) sulfate Chemical compound [Mn+2].[O-]S([O-])(=O)=O SQQMAOCOWKFBNP-UHFFFAOYSA-L 0.000 description 1
- 229910000357 manganese(II) sulfate Inorganic materials 0.000 description 1
- 238000004519 manufacturing process Methods 0.000 description 1
- 230000002906 microbiologic effect Effects 0.000 description 1
- CUXQLKLUPGTTKL-UHFFFAOYSA-M microcosmic salt Chemical compound [NH4+].[Na+].OP([O-])([O-])=O CUXQLKLUPGTTKL-UHFFFAOYSA-M 0.000 description 1
- 239000000203 mixture Substances 0.000 description 1
- 238000012986 modification Methods 0.000 description 1
- 230000004048 modification Effects 0.000 description 1
- 235000019837 monoammonium phosphate Nutrition 0.000 description 1
- 239000006012 monoammonium phosphate Substances 0.000 description 1
- 229910000402 monopotassium phosphate Inorganic materials 0.000 description 1
- 235000019796 monopotassium phosphate Nutrition 0.000 description 1
- 229910052757 nitrogen Inorganic materials 0.000 description 1
- 230000008520 organization Effects 0.000 description 1
- GNSKLFRGEWLPPA-UHFFFAOYSA-M potassium dihydrogen phosphate Chemical compound [K+].OP(O)([O-])=O GNSKLFRGEWLPPA-UHFFFAOYSA-M 0.000 description 1
- 230000003389 potentiating effect Effects 0.000 description 1
- 239000000843 powder Substances 0.000 description 1
- 238000001556 precipitation Methods 0.000 description 1
- 238000002360 preparation method Methods 0.000 description 1
- 239000012857 radioactive material Substances 0.000 description 1
- 238000004062 sedimentation Methods 0.000 description 1
- 239000006152 selective media Substances 0.000 description 1
- 239000011780 sodium chloride Substances 0.000 description 1
- 239000002689 soil Substances 0.000 description 1
- 239000007787 solid Substances 0.000 description 1
- 239000004071 soot Substances 0.000 description 1
- 238000005507 spraying Methods 0.000 description 1
- 239000000126 substance Substances 0.000 description 1
- 150000004763 sulfides Chemical class 0.000 description 1
- 238000012360 testing method Methods 0.000 description 1
- 229960000344 thiamine hydrochloride Drugs 0.000 description 1
- 235000019190 thiamine hydrochloride Nutrition 0.000 description 1
- 239000011747 thiamine hydrochloride Substances 0.000 description 1
- DPJRMOMPQZCRJU-UHFFFAOYSA-M thiamine hydrochloride Chemical compound Cl.[Cl-].CC1=C(CCO)SC=[N+]1CC1=CN=C(C)N=C1N DPJRMOMPQZCRJU-UHFFFAOYSA-M 0.000 description 1
- 241001478887 unidentified soil bacteria Species 0.000 description 1
- 238000012795 verification Methods 0.000 description 1
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Chemical compound O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 1
- 229910052984 zinc sulfide Inorganic materials 0.000 description 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C12—BIOCHEMISTRY; BEER; SPIRITS; WINE; VINEGAR; MICROBIOLOGY; ENZYMOLOGY; MUTATION OR GENETIC ENGINEERING
- C12Q—MEASURING OR TESTING PROCESSES INVOLVING ENZYMES, NUCLEIC ACIDS OR MICROORGANISMS; COMPOSITIONS OR TEST PAPERS THEREFOR; PROCESSES OF PREPARING SUCH COMPOSITIONS; CONDITION-RESPONSIVE CONTROL IN MICROBIOLOGICAL OR ENZYMOLOGICAL PROCESSES
- C12Q1/00—Measuring or testing processes involving enzymes, nucleic acids or microorganisms; Compositions therefor; Processes of preparing such compositions
- C12Q1/02—Measuring or testing processes involving enzymes, nucleic acids or microorganisms; Compositions therefor; Processes of preparing such compositions involving viable microorganisms
- C12Q1/04—Determining presence or kind of microorganism; Use of selective media for testing antibiotics or bacteriocides; Compositions containing a chemical indicator therefor
Definitions
- air mass movement is important in weather forecasting where it is often monitored by examining changes in ambient atmospheric pressure.
- Studies of the phenomenon of acid rain, industrial plant emissions or of chemical or biological weapon attacks also need physical verification of the expected movement of the air masses involved in order to ascertain whether various predictions or assumptions are valid.
- One of the present means of monitoring the movement of an air mass has been by releasing fluorescent particles of zinc cadmium sulfide or zinc sulfide into the air and sometimes by the release of a radioactive particle.
- a sample of the air mass is collected downwind.
- the presence of the fluorescent particles or radioactive particles in the collected sample is thereafter determined using suitable equipment such as, for example, a fluorometer or a radioactive counter.
- suitable equipment such as, for example, a fluorometer or a radioactive counter.
- cadmium is known to be toxic and therefore its use is undesirable. It is also undesirable to release sulfides into the atmosphere or to release radioactive materials into the atmosphere. Accordingly, a need exists for a safe and reliable method of tracing air mass movement.
- This invention relates to a method of monitoring the movement of an air mass and more particularly to the monitoring of the movement of an air mass by releasing a tracer entity at a given location, collecting a sample of the air at a different location and analyzing the collected sample of air for the presence of the tracer entity in which the tracer entity is Bacillus thurengiensis and the analysis is effected by culturing the collected sample on a medium capable of supporting bacterium growth.
- the growth medium contains citrate as the sole source of assimilable carbon.
- the movement of an air mass is monitored by introducing a quantity of Bacillus thurengiensis into the atmosphere at one or more given locations and positioning sampling equipment one or more points of interest to collect all of the material present in the ambient air.
- the collection equipment is usually placed downwind of the release point, but may also be in other locations to determine if there are any unexplained or unexpected movement of the air.
- a plurality of collection points forming a more or less regular grid pattern is established in order to achieve a more complete plot of the air's movement.
- Bacillus thurengiensis is a widely used entomopathogen. It was originally isolated from natural epizootics in susceptible Lepidopteria in Japan and Germany. Various formulations of Bacillus thurengiensis have been commercially available for use in agriculture since the mid-1950s. A potent strain was introduced commercially in the 1970s under the trademark DIPEL. In 1977, a further strain named Bacillus thurengiensis var israelensis was isolated in a stagnant pool in a river bed in the Negev Desert and later designated as Bacillus thurengiensis, Serotype H-14. The World Health Organization has developed a standard preparation of Serotype H-14 under the designation IPS-78.
- Bacillus thurengiensis is a spore forming, very hardy bacterium which is safe for warmblooded animals including humans. As a practical matter, the bacterium is an insecticide only for caterpillars and mosquitoes and it is not persistant in the environment. These characteristics make the Bacillus thurengiensis particularly useful in the present invention.
- the bacterium In order to trace the movement of an air mass, the bacterium is released into the atmosphere as a cloud of wet or dry particles generally, but not necessarily, in the 2-5 micron range.
- the bacterium can be released into the atmosphere in the same manner as it is used as a selective insecticide.
- a land-based atomizer or aerial spraying can be employed.
- the quantity released is not critical and theoretically a single spore is all that is necessary. More practically, a quantity of about 110-230 grams of Bacillus thurengiensis powder (having a potency of 1000 to 2000 Aedes Aegypti International Toxic Units) can be employed per release location but greater but lesser amounts can also be employed, if desired.
- Any conventional method of collecting airborne bacteria can be employed at the collection point or points in the process of this invention.
- the basic methods which can be employed include impingement in liquids, impaction on solid surfaces, filtration, sedimentation, centrifugation, electrostatic precipitation and thermal precipitation.
- a wide variety of instruments are available for practicing these collection methods. An excellent survey of these sampling methods and the equipment employed therein can be found in "Sampling Microbiological Aerosols", Public Health Monograph No. 60, issued by the Public Health Service of the U.S. Department of Health, Education and Welfare (Public Health Service Publication No. 686).
- the airborne detrius i.e., the material found in the ambient air, various pollens, fungi, spores, soil bacteria, soil particles, soot and assorted man-made particles, in the collected sample or samples is cultured, i.e., the collected fraction of particulates in the atmosphere are combined with a suitable culture medium which can support the growth of the bacterium.
- Bacillus thurengiensis is particularly advantageous for two reasons.
- the microbe grows at room temperature so that no complex equipment is needed.
- the bacterium is unusual in that it can metabolize the citrate ion as a source of carbon while almost all other known spore forming bacteria are not so capable.
- the inclusion of citrate in an acidic state also inhibits the growth of other microbes.
- the culture can be effected in any medium capable of supporting growth, it is preferably carried out in a medium containing citrate as the sole source of assimilable carbon.
- a medium containing citrate as the sole source of assimilable carbon.
- Any of the known citrate media which do not contain another assimilable carbon source can be employed.
- a particular advantageous medium is the Koser Citrate Medium which in dehydrated form contains 1.5 grams of sodium ammonium phosphate, 1 gram of mono-potassium phosphate, 0.2 gram magnesium sulfate and 3 grams of sodium citrate.
- the ammonium salt serves as the sole source of nitrogen and the sodium citrate as the sole source of carbon.
- To rehydrate this medium 5.7 grams are dissolved in 100 ml of distilled water.
- Another typical citrate medium is Simmons Citrate Agar which contains 0.2 gram magnesium sulfate, 1 gram of monoammonium phosphate, 1 gram dipotassium phosphate, 2 grams sodium citrate, 5 grams sodium chloride, 15 grams agar and 0.08 gram bromthymol blue.
- a typical culture medium which can be used in the present invention will contain 5.7 grams per liter Koser Citrate Medium, 10 grams per liter caseine enzymatic digest, 0.03 gram per liter MnSO 4 , 0.02 grams per liter FeSO 4 , 0.002 gram per liter thiamine hydrochloride and 15 grams per liter agar. Since only one Bacillus thurengiensis spore is needed in order to detect its presence, the test of the present invention is very sensitive. The single spore grows and replicates itself many times.
- An example of one use of the present invention concerns an evaluation of the accusation that fluoride emissions from an aluminum plant was killing cattle located at a distance of about 10 miles from the production plant.
- a solution of Bacillus thurengiensis spores is sprayed into the atmosphere at the plant site under various weather conditions and collection devices are installed at the location where the cattle deaths occurred.
- the collected material is then cultured in the selective medium to determine the presence or absence of the bacterium. Since both the fluoride emissions and the bacterium will be carried away from the aluminum plant by the same air mass, the results of the culturing provides an indication of whether the fluoride may have traveled from the plant to the place of the cattle fatalities.
Landscapes
- Chemical & Material Sciences (AREA)
- Life Sciences & Earth Sciences (AREA)
- Health & Medical Sciences (AREA)
- Organic Chemistry (AREA)
- Engineering & Computer Science (AREA)
- Zoology (AREA)
- Wood Science & Technology (AREA)
- Proteomics, Peptides & Aminoacids (AREA)
- Analytical Chemistry (AREA)
- Toxicology (AREA)
- Immunology (AREA)
- Microbiology (AREA)
- Molecular Biology (AREA)
- Biophysics (AREA)
- Physics & Mathematics (AREA)
- Biotechnology (AREA)
- Biochemistry (AREA)
- Bioinformatics & Cheminformatics (AREA)
- General Engineering & Computer Science (AREA)
- General Health & Medical Sciences (AREA)
- Genetics & Genomics (AREA)
- Micro-Organisms Or Cultivation Processes Thereof (AREA)
Abstract
The movement of an air mass is monitored by releasing a tracer entity at aiven location, collecting a sample of air at a different location and analyzing the collected sample of air for the presence of the tracer entity by using Bacillus thurengiensis as the tracer entity and by analyzing for the presence of the bacterium by effecting a culture in a medium capable of supporting bacterial growth and preferably containing citrate as the sole source of assimilable carbon.
Description
It is frequently desirable to monitor or track the movement of a mass of air. For example, air mass movement is important in weather forecasting where it is often monitored by examining changes in ambient atmospheric pressure. Studies of the phenomenon of acid rain, industrial plant emissions or of chemical or biological weapon attacks also need physical verification of the expected movement of the air masses involved in order to ascertain whether various predictions or assumptions are valid.
Theoretical discussions of air mass movement can be found in the "Air Pollution Handbook", McGill et al. (McGraw-Hill Book Co., 1956) Section 4-54 at pp. 54-59; Sutton, "Atmospheric Turbulence" (John Wiley & Sons, 1949); and Sutton, "Micrometeorology" (McGraw-Hill Book Co., 1953).
One of the present means of monitoring the movement of an air mass has been by releasing fluorescent particles of zinc cadmium sulfide or zinc sulfide into the air and sometimes by the release of a radioactive particle. A sample of the air mass is collected downwind. The presence of the fluorescent particles or radioactive particles in the collected sample is thereafter determined using suitable equipment such as, for example, a fluorometer or a radioactive counter. However, cadmium is known to be toxic and therefore its use is undesirable. It is also undesirable to release sulfides into the atmosphere or to release radioactive materials into the atmosphere. Accordingly, a need exists for a safe and reliable method of tracing air mass movement.
It is accordingly the object of this invention to provide a method for the monitoring of the movement of an air mass without the release of toxic, radioactive or other undesirable material into the atmosphere. This and other objects of the invention will become apparent to those of ordinary skill in this art from the following detailed disclosure.
This invention relates to a method of monitoring the movement of an air mass and more particularly to the monitoring of the movement of an air mass by releasing a tracer entity at a given location, collecting a sample of the air at a different location and analyzing the collected sample of air for the presence of the tracer entity in which the tracer entity is Bacillus thurengiensis and the analysis is effected by culturing the collected sample on a medium capable of supporting bacterium growth. Preferably, the growth medium contains citrate as the sole source of assimilable carbon.
In accordance with the present invention, the movement of an air mass is monitored by introducing a quantity of Bacillus thurengiensis into the atmosphere at one or more given locations and positioning sampling equipment one or more points of interest to collect all of the material present in the ambient air. The collection equipment is usually placed downwind of the release point, but may also be in other locations to determine if there are any unexplained or unexpected movement of the air. Frequently, a plurality of collection points forming a more or less regular grid pattern is established in order to achieve a more complete plot of the air's movement.
Bacillus thurengiensis is a widely used entomopathogen. It was originally isolated from natural epizootics in susceptible Lepidopteria in Japan and Germany. Various formulations of Bacillus thurengiensis have been commercially available for use in agriculture since the mid-1950s. A potent strain was introduced commercially in the 1970s under the trademark DIPEL. In 1977, a further strain named Bacillus thurengiensis var israelensis was isolated in a stagnant pool in a river bed in the Negev Desert and later designated as Bacillus thurengiensis, Serotype H-14. The World Health Organization has developed a standard preparation of Serotype H-14 under the designation IPS-78.
Bacillus thurengiensis is a spore forming, very hardy bacterium which is safe for warmblooded animals including humans. As a practical matter, the bacterium is an insecticide only for caterpillars and mosquitoes and it is not persistant in the environment. These characteristics make the Bacillus thurengiensis particularly useful in the present invention.
In order to trace the movement of an air mass, the bacterium is released into the atmosphere as a cloud of wet or dry particles generally, but not necessarily, in the 2-5 micron range. The bacterium can be released into the atmosphere in the same manner as it is used as a selective insecticide. For example, one can use a land-based atomizer or aerial spraying can be employed. The quantity released is not critical and theoretically a single spore is all that is necessary. More practically, a quantity of about 110-230 grams of Bacillus thurengiensis powder (having a potency of 1000 to 2000 Aedes Aegypti International Toxic Units) can be employed per release location but greater but lesser amounts can also be employed, if desired.
Any conventional method of collecting airborne bacteria can be employed at the collection point or points in the process of this invention. The basic methods which can be employed include impingement in liquids, impaction on solid surfaces, filtration, sedimentation, centrifugation, electrostatic precipitation and thermal precipitation. A wide variety of instruments are available for practicing these collection methods. An excellent survey of these sampling methods and the equipment employed therein can be found in "Sampling Microbiological Aerosols", Public Health Monograph No. 60, issued by the Public Health Service of the U.S. Department of Health, Education and Welfare (Public Health Service Publication No. 686).
The airborne detrius, i.e., the material found in the ambient air, various pollens, fungi, spores, soil bacteria, soil particles, soot and assorted man-made particles, in the collected sample or samples is cultured, i.e., the collected fraction of particulates in the atmosphere are combined with a suitable culture medium which can support the growth of the bacterium.
Beyond the known safety to humans, plants, domestic animals and almost all lower life forms, and the established methods of introduction into the atmosphere, the use of Bacillus thurengiensis is particularly advantageous for two reasons. First, the microbe grows at room temperature so that no complex equipment is needed. Second, the bacterium is unusual in that it can metabolize the citrate ion as a source of carbon while almost all other known spore forming bacteria are not so capable. Further, the inclusion of citrate in an acidic state also inhibits the growth of other microbes. These characteristics simplify the analysis procedure and provide for greater accuracy since the growth of other spore forming bacteria need not be distinguished in the medium. Accordingly, while the culture can be effected in any medium capable of supporting growth, it is preferably carried out in a medium containing citrate as the sole source of assimilable carbon. Any of the known citrate media which do not contain another assimilable carbon source can be employed.
A particular advantageous medium is the Koser Citrate Medium which in dehydrated form contains 1.5 grams of sodium ammonium phosphate, 1 gram of mono-potassium phosphate, 0.2 gram magnesium sulfate and 3 grams of sodium citrate. In this medium, the ammonium salt serves as the sole source of nitrogen and the sodium citrate as the sole source of carbon. To rehydrate this medium, 5.7 grams are dissolved in 100 ml of distilled water. Another typical citrate medium is Simmons Citrate Agar which contains 0.2 gram magnesium sulfate, 1 gram of monoammonium phosphate, 1 gram dipotassium phosphate, 2 grams sodium citrate, 5 grams sodium chloride, 15 grams agar and 0.08 gram bromthymol blue.
A typical culture medium which can be used in the present invention will contain 5.7 grams per liter Koser Citrate Medium, 10 grams per liter caseine enzymatic digest, 0.03 gram per liter MnSO4, 0.02 grams per liter FeSO4, 0.002 gram per liter thiamine hydrochloride and 15 grams per liter agar. Since only one Bacillus thurengiensis spore is needed in order to detect its presence, the test of the present invention is very sensitive. The single spore grows and replicates itself many times.
An example of one use of the present invention concerns an evaluation of the accusation that fluoride emissions from an aluminum plant was killing cattle located at a distance of about 10 miles from the production plant. A solution of Bacillus thurengiensis spores is sprayed into the atmosphere at the plant site under various weather conditions and collection devices are installed at the location where the cattle deaths occurred. The collected material is then cultured in the selective medium to determine the presence or absence of the bacterium. Since both the fluoride emissions and the bacterium will be carried away from the aluminum plant by the same air mass, the results of the culturing provides an indication of whether the fluoride may have traveled from the plant to the place of the cattle fatalities.
Various changes and modifications can be made in the method of this invention without departing from the spirit and scope thereof. The various embodiments which have been disclosed herein were for the purpose of further illustrating the present invention and were not intended to limit it.
Claims (5)
1. In a method of monitoring the movement of an air mass comprising releasing a tracer entity into the atmosphere at a given location, collecting a sample of the ambient air at a different location and analyzing the sample of the collected air for the presence of the tracer entity, the improvement which comprises employing Bacillus thurengiensis as the tracer entity and conducting the analysis by performing a culture on the collected sample in a medium capable of supporting Bacillus thurengiensis growth.
2. The method of claim 1 in which samples of air are collected at a plurality of locations.
3. The method of claim 2 in which said medium contains citrate as the sole source of assimilable carbon.
4. The method of claim 3 wherein the culture medium contains Koser Citrate Medium.
5. The method of claim 1 in which said medium contains citrate as the sole source of assimilable carbon.
Priority Applications (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US06/799,531 USH110H (en) | 1985-11-14 | 1985-11-14 | Tracking of air mass movement |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US06/799,531 USH110H (en) | 1985-11-14 | 1985-11-14 | Tracking of air mass movement |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| USH110H true USH110H (en) | 1986-08-05 |
Family
ID=25176149
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| US06/799,531 Abandoned USH110H (en) | 1985-11-14 | 1985-11-14 | Tracking of air mass movement |
Country Status (1)
| Country | Link |
|---|---|
| US (1) | USH110H (en) |
Cited By (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US4735899A (en) | 1985-03-11 | 1988-04-05 | The Baker Company, Inc. | Detection of airborne microorganisms |
-
1985
- 1985-11-14 US US06/799,531 patent/USH110H/en not_active Abandoned
Cited By (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US4735899A (en) | 1985-03-11 | 1988-04-05 | The Baker Company, Inc. | Detection of airborne microorganisms |
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