U.S. patent application number 13/984488 was filed with the patent office on 2014-08-21 for microbial inoculants and fertilizer compositions comprising the same.
The applicant listed for this patent is International Marketing Partnerships Pty Ltd. Invention is credited to Wayne Finlayson, Karen Jury.
Application Number | 20140230504 13/984488 |
Document ID | / |
Family ID | 48191121 |
Filed Date | 2014-08-21 |
United States Patent
Application |
20140230504 |
Kind Code |
A1 |
Finlayson; Wayne ; et
al. |
August 21, 2014 |
MICROBIAL INOCULANTS AND FERTILIZER COMPOSITIONS COMPRISING THE
SAME
Abstract
Provided herein are microbial inoculants for use in increasing
plant growth, plant productivity and/or soil quality, comprising
strains of one or more bacterial species selected from
Lactobacillus parafarraginis, Lactobacillus buchneri, Lactobacillus
rapi and Lactobacillus zeae. Optionally the microbial inoculants
also comprise a strain of Acetobacter fabarum and/or a strain of
Candida ethanolica. Also provided are fertilizer compositions
comprising said microbial inoculants.
Inventors: |
Finlayson; Wayne; (Varsity
Lakes, AU) ; Jury; Karen; (East Ballina, AU) |
|
Applicant: |
Name |
City |
State |
Country |
Type |
International Marketing Partnerships Pty Ltd |
East Melbourne |
|
AU |
|
|
Family ID: |
48191121 |
Appl. No.: |
13/984488 |
Filed: |
November 5, 2012 |
PCT Filed: |
November 5, 2012 |
PCT NO: |
PCT/AU2012/001355 |
371 Date: |
August 8, 2013 |
Related U.S. Patent Documents
|
|
|
|
|
|
Application
Number |
Filing Date |
Patent Number |
|
|
61555535 |
Nov 4, 2011 |
|
|
|
Current U.S.
Class: |
71/6 ;
435/252.9 |
Current CPC
Class: |
C12R 1/02 20130101; C12R
1/225 20130101; Y02W 30/43 20150501; C05F 17/939 20200101; C12N
1/20 20130101; C05F 11/08 20130101; C12N 1/16 20130101; C05F 11/02
20130101; Y02P 20/145 20151101; Y02W 30/40 20150501; C12R 1/72
20130101; C05F 11/02 20130101; C05F 11/08 20130101 |
Class at
Publication: |
71/6 ;
435/252.9 |
International
Class: |
C05F 11/08 20060101
C05F011/08; C12R 1/225 20060101 C12R001/225 |
Claims
1. A microbial inoculant for use in increasing plant growth, plant
productivity and/or soil quality, comprising strains of one or more
bacterial species selected from Lactobacillus parafarraginis,
Lactobacillus buchneri, Lactobacillus rapi and Lactobacillus
zeae.
2-4. (canceled)
5. A microbial inoculant according to any one of claim 1 wherein
the inoculant is a symbiotic combination of two or more, or three
or more, of said Lactobacillus species.
6. A microbial inoculant according to claim 1 wherein the
Lactobacillus parafarraginis strain is Lactobacillus parafarraginis
Lp18 deposited with National Measurement Institute, Australia on 27
Oct. 2011 under Accession Number V11/022945.
7. (canceled)
8. A microbial inoculant according to claim 1 wherein the
Lactobacillus buchneri strain is Lactobacillus buchneri Lb23
deposited with National Measurement Institute, Australia on 27 Oct.
2011 under Accession Number V11/022946.
9. (canceled)
10. A microbial inoculant according to claim 1 wherein the
Lactobacillus rapi strain is Lactobacillus rapi Lr24 deposited with
National Measurement Institute, Australia on 27 Oct. 2011 under
Accession Number V11/022947.
11. (canceled)
12. A microbial inoculant according to claim 1 wherein the
Lactobacillus zeae strain is Lactobacillus zeae Lz26 deposited with
National Measurement Institute, Australia on 27 Oct. 2011 under
Accession Number V11/022948.
13. (canceled)
14. A microbial inoculant according to claim 1 further comprising a
strain of Acetobacter fabarum.
15. A microbial inoculant according to claim 14 wherein the
Acetobacter fabarum strain is Acetobacter fabarum Af15 deposited
with the National Measurement Institute, Australia on 27 Oct. 2011
under Accession Number V11/022943.
16. (canceled)
17. A microbial inoculant according to claim 1 further comprising a
yeast.
18. A microbial inoculant according to claim 17 wherein the yeast
is a strain of Candida ethanolica.
19. A microbial inoculant according to claim 18 wherein the Candida
ethanolica strain is Candida ethanolica Ce31 deposited with the
National Measurement Institute, Australia on 27 Oct. 2011 under
Accession Number V11/022944.
20. (canceled)
21. A microbial inoculant according to claim 1 wherein one or more
of the strains in the inoculant is encapsulated.
22-23. (canceled)
24. An inoculant according to claim 1 for use as a fertilizer.
25. A fertilizer composition comprising a microbial inoculant
according to claim 1.
26. (canceled)
27. A fertilizer composition according to claim 25 for use in
fertilizing pasture plants, crop plants or ornamental plants.
28. A fertilizer composition according to claim 27 wherein the crop
is a human or animal food crop or crop for use as fuel or for
pharmaceutical production.
29. A fertilizer composition according to claim 28 wherein the food
crop is a fruit, vegetable, nut, seed or grain.
30. A method for increasing plant growth and/or productivity, the
method comprising applying to the plant, plant seeds or to the soil
in which the plant or plant seeds are grown an effective amount of
a microbial inoculant according to claim 1 or a fertilizer
composition according to claim 25.
31. A method for improving soil quality or remediating degraded
soil or pasture, the method comprising applying to the soil or
pasture, or to the plants or plant seeds in said soil, an effective
amount of a microbial inoculant according to any one of claims 1 to
24 claim 1 or a fertilizer composition according to claim 25.
32. A method according to claim 30 or 31 wherein the plant is a
pasture plant, crop plant or ornamental plant.
33-34. (canceled)
Description
FIELD OF THE ART
[0001] The present disclosure relates generally to microbial
inoculants, particularly for use as fertilizers, comprising one or
more microbial species or strains as described herein, and to
fertilizer compositions comprising such organisms. The disclosure
also relates to methods of promoting plant growth, increasing
availability of nutrients in the soil and remediating degraded
soils and pastures using microbial inoculants and fertilizer
compositions of the present disclosure.
BACKGROUND
[0002] The use of fertilizers to enhance plant and crop production
and overcome poor soil quality is widespread. Most commonly
employed commercially available fertilizers are inorganic chemical
fertilizers. Such chemical fertilizers can be expensive to produce,
can be hazardous to use and are often associated with
environmentally damaging consequences, such as nitrate
contamination in run off and ground water. Environmental
sustainability can be promoted by limiting the use of chemical
fertilizers.
[0003] Fertilizer compositions comprising microorganisms (so-called
"biofertilizers") are increasingly considered as alternatives to
conventional chemical fertilizers. The ability of specific
bacterial species to promote plant growth has long been recognised.
For example, nitrogen-fixing bacteria such as Rhizobium species
provide plants with essential nitrogenous compounds. Species of
Azotobacter and Azospirillum have also been shown to promote plant
growth and increase crop yield, promoting the accumulation of
nutrients in plants. However bacteria of these genera are often
unable to compete effectively with native soil and plant flora,
thereby requiring the application of impractically large volumes of
inoculum. Various Bacillus and Pseudomonas species have also found
application in microbial-based fertilizers.
[0004] To date, biofertilizers have typically met with limited
success, often not proving to be efficacious under real farming
conditions. There remains a need for improved microbial-based
fertilizers that are effective in providing nutrients for plant
growth and are environmentally safe and nonhazardous.
SUMMARY OF THE DISCLOSURE
[0005] A first aspect of the present disclosure provides a
microbial inoculant for use in increasing plant growth, plant
productivity and/or soil quality, comprising strains of one or more
bacterial species selected from Lactobacillus parafarraginis,
Lactobacillus buchneri, Lactobacillus rapi and Lactobacillus
zeae.
[0006] In a particular embodiments the inoculant comprises two of
said Lactobacillus species, three of said Lactobacillus species or
all of said Lactobacillus species. The inoculant may represent a
symbiotic combination of two or more or three or more of said
Lactobacillus species.
[0007] The Lactobacillus parafarraginis strain may be Lactobacillus
parafarraginis Lp18. In a particular embodiment the Lactobacillus
parafarraginis strain is Lactobacillus parafarraginis Lp18
deposited with National Measurement Institute, Australia on 27 Oct.
2011 under Accession Number V11/022945.
[0008] The Lactobacillus buchneri strain may be Lactobacillus
buchneri Lb23. In a particular embodiment the Lactobacillus
buchneri strain is Lactobacillus buchneri Lb23 deposited with
National Measurement Institute, Australia on 27 Oct. 2011 under
Accession Number V11/022946.
[0009] The Lactobacillus rapi strain may be Lactobacillus rapi
Lr24. In a particular embodiment the Lactobacillus rapi strain is
Lactobacillus rapi Lr24 deposited with National Measurement
Institute, Australia on 27 Oct. 2011 under Accession Number
V11/022947.
[0010] The Lactobacillus zeae strain may be Lactobacillus zeae
Lz26. In a particular embodiment the Lactobacillus zeae strain is
Lactobacillus zeae. Lz26 deposited with National Measurement
Institute, Australia on 27 Oct. 2011 under Accession Number
V11/022948.
[0011] An inoculant of the first aspect may further comprise a
strain of Acetobacter fabarum. The Acetobacter fabarum strain may
be Acetobacter fabarum Af15. In a particular embodiment the
Acetobacter fabarum strain is Acetobacter fabarum Af15 deposited
with the National Measurement Institute, Australia on 27 Oct. 2011
under Accession Number V11/022943.
[0012] An inoculant of the first aspect may further comprise a
yeast. The yeast may be a strain of Candida ethanolica. The Candida
ethanolica strain may be Candida ethanolica Ce31. In a particular
embodiment the Candida ethanolica strain is Candida ethanolica Ce31
deposited with the National Measurement Institute, Australia on 27
Oct. 2011 under Accession Number V11/022944.
[0013] One or more of the strains in the inoculant may be
encapsulated. Where multiple strains are encapsulated, the strains
may be individually' encapsulated or combined in a single
encapsulation.
[0014] A second aspect of the present disclosure provides a
microbial inoculant comprising at least one Lactobacillus species,
at least one Acetobacter species and at least one Candida
species.
[0015] In a particular embodiment the at least one Lactobacillus
species is selected from Lactobacillus parafarraginis,
Lactobacillus buchneri, Lactobacillus rapi and Lactobacillus zeae.
In a further particular embodiment, the microbial inoculant
comprises at least one strain of each of said Lactobacillus
species. In a further particular embodiment, the Lactobacillus
parafarraginis is strain Lp18 (deposited under Accession Number
V11/022945), Lactobacillus buchneri is strain Lb23 (deposited under
Accession Number V11/022946), Lactobacillus rapi is strain Lr24
(deposited under Accession Number V11/022947) and Lactobacillus
zeae is strain Lz26 (deposited under Accession Number
V11/022948).
[0016] In a particular embodiment the at least one Acetobacter
species is Acetobacter fabarum. In a further particular embodiment
the Acetobacter fabarum is Af15 (deposited under Accession Number
V11/022943).
[0017] In a particular embodiment the at least one Candida species
is Candida ethanolica. In a further particular embodiment the
Candida ethanolica is Ce31 (deposited under Accession Number
V11/022944).
[0018] A third aspect of the present disclosure provides a
microbial inoculant comprising at least one bacterial strain
selected from Lactobacillus parafarraginis Lp18, Lactobacillus
buchneri Lb23, Lactobacillus rapi Lr24 and Lactobacillus zeae
Lz26.
[0019] An inoculant of the third aspect optionally further
comprises Acetobacter fabarum Af15 and/or Candida ethanolica
Ce31.
[0020] An inoculant, of the first, second or third aspect may be
used as a fertilizer.
[0021] A fourth aspect of the present disclosure provides a
fertilizer composition comprising a microbial inoculant of the
first, second or third aspect. The fertilizer composition may
optionally comprise one or more additional components such as
organic material, humic substances, penetrants, macronutrients,
micronutrients and other soil and/or plant additives.
[0022] A fifth aspect of the present disclosure provides a method
for increasing plant growth and/or productivity, the method
comprising applying to the plant, plant seeds or to the soil in
which the plant or plant seeds are grown an effective amount of a
microbial inoculant of the first, second or third aspect or a
fertilizer composition of the fourth aspect.
[0023] A sixth aspect of the present disclosure provides a method
for improving soil quality, the method comprising applying to soil
or to the plants or plant seeds in said soil an effective amount of
a microbial inoculant of the first, second or third aspect or a
fertilizer composition of the fourth aspect.
[0024] In accordance with the above aspects the plant may be, for
example, a pasture plant, crop plant (including fruit and vegetable
plants) or ornamental plant. The crop may be, for example, any
human or animal food crop or crop for use as fuel or for
pharmaceutical production. The food crop may be, for example, a
fruit, vegetable, nut, seed or grain.
[0025] A seventh aspect of the present disclosure provides a method
for remediating degraded soil or pasture, the method comprising
applying to the soil or pasture an effective amount of a microbial
inoculant of the first, second or third aspect or a fertilizer
composition of the fourth aspect.
BRIEF DESCRIPTION OF THE DRAWINGS
[0026] Aspects and embodiments of the present disclosure are
described herein, by way of non-limiting example only, with
reference to the following drawings.
[0027] FIG. 1. Root development in tick bean plants, treated as
described in Example 5. A, control group; B, T40 treatment group;
C, SGL40 treatment group; D, T25% GL40 treatment group; E, GL40
treatment group.
[0028] FIG. 2. Average rate of change of growth (height) of tomato
plants over a 20 day treatment period in three different soils
(A-C), treated as described in Example 6. Squares represent IMP Bio
treated seedlings, diamonds represent FlowPhos treated seedlings,
triangles represent IMP Bio plus FlowPhos treated seedlings,
crosses (`x`) represent untreated (water only) seedlings.
[0029] FIG. 3. Comparison of plant height, foliage size and root
development in tomato seedlings, treated as described in Example 6.
GreatLand=IMP Bio treated seedling.
[0030] FIG. 4. Comparison of vegetative growth (and density of
growth) of strawberry plants, treated as described in Example 8. A,
conventional fertilizer treated plants after 3 months. B, IMP Bio
treated plants after 3 months.
DETAILED DESCRIPTION
[0031] Unless defined otherwise, all technical and scientific terms
used herein have the same meaning as commonly understood by those
of ordinary skill in the art to which the disclosure belongs.
Although any methods and materials similar or equivalent to those
described herein can be used in the practice or testing of the
present disclosure, typical methods and materials are
described.
[0032] The articles "a" and "an" are used herein to refer to one or
to more than one (i.e., to at least one) of the grammatical object
of the article. By way of example, "an element" means one element
or more than one element.
[0033] In the context of this specification, the term "about," is
understood to refer to a range of numbers that a person of skill in
the art would consider equivalent to the recited value in the
context of achieving the same function or result.
[0034] Throughout, this specification and the claims which follow,
unless the context requires otherwise, the word "comprise", and
variations such as "comprises" or "comprising", will be understood
to imply the inclusion of a stated integer or step or group of
integers or steps but not the exclusion of any other integer or
step or group of integers or steps.
[0035] The term "plant productivity" as used herein refers to any
aspect of growth or development of a plant, that is a reason for
which the plant is grown. Thus, for purposes of the present
disclosure, improved or increased plant productivity refers broadly
to improvements in biomass or yield of leaves, stems, grain, fruit,
vegetables, flowers, or other plant parts harvested or used for
various purposes, and improvements in growth of plant parts,
including stems, leaves and roots. For example, when referring to
food crops, such as grains, fruits or vegetables, plant
productivity may refer to the yield of grain, fruit, vegetables or
seeds harvested from a particular crop. For crops such as pasture,
plant productivity may refer to growth rate, plant density or the
extent of groundcover. "Plant growth" refers to the growth of any,
plant part, including stems, leaves and roots. Growth may refer to
the rate of growth of any one of these plant parts.
[0036] The term "yield" refers to the amount of produced biological
material and may be used interchangeably with "biomass". For crop
plants, "yield" may also mean the amount of harvested material per
unit of production or per area (e.g. hectare). Yield may be defined
in terms of quantity or quality. The harvested material may vary
from crop to crop, for example, it may be seeds, above-ground
biomass, below-ground biomass (e.g. potatoes), roots, fruits, or
any other part of the plant which is of economic value. "Yield"
also encompasses yield stability of the plants. "Yield" also
encompasses yield potential, which is the maximum obtainable yield
under optimal growth conditions. Yield may be dependent on a number
of yield components, which may be monitored by certain parameters.
These parameters are well known to persons skilled in the art and
vary from crop to crop. For example, breeders are well aware of the
specific yield components and the corresponding parameters for the
crop they are aiming to improve. For example, key yield parameters
for potato include tuber weight, number of tubers, and number of
stems per plant.
[0037] By "improving soil quality" is meant increasing the amount
and/or availability of nutrients required by, or beneficial to
plants, for growth. By way of example only, such nutrients include
nitrogen, phosphorous, potassium, copper, zinc, boron and
molybdenum. Also encompassed by the term "improving soil quality"
is reducing or minimising the amount of an element that may be
detrimental to plant growth or development such as, for example
iron and manganese. Thus, improving soil quality by use of
microbial inoculants and fertilizer compositions of the present
disclosure thereby assists and promotes the growth of plants in the
soil.
[0038] The term "remediating" as used herein in relation to
degraded pasture or soil refers to the improvement in plant
nutrient content in the soil to facilitate improved plant growth
and/or yield. Degraded pasture includes overgrazed pasture.
[0039] As used herein, the term "effective amount" refers to an
amount of microbial inoculant or fertilizer composition applied to
a given area of soil or vegetation that is sufficient to effect one
or more beneficial or desired outcomes, for example, in terms of
plant growth rates, crop yields, or nutrient availability in the
soil. An "effective amount" can be provided in one or more
administrations. The exact amount required will vary depending on
factors such as the identity and number of individual strains
employed, the plant species being treated, the nature and condition
of the soil to be treated, the exact nature of the microbial
inoculant or fertilizer composition to be applied, the form in
which the inoculant or fertilizer is applied and the means by which
it is applied, and the stage of the plant growing season during
which application takes place. Thus, it is not possible to specify
an exact "effective amount". However, for any given case, an
appropriate "effective amount" may be determined by one of ordinary
skill in the art using only routine experimentation.
[0040] The term "crop" as used herein refers to any plant grown to
be harvested or used for any economic purpose, including for
example human foods, livestock fodder, fuel or pharmaceutical
production (e.g. poppies).
[0041] The term "optionally" is used herein to mean that the
subsequently described feature may or may not be present or that
the subsequently described event or circumstance may or may not
occur. Hence the specification will be understood to include and
encompass embodiments in which the feature is present and
embodiments in which the feature is not present, and embodiments in
which the event or circumstance occurs as well as embodiments in
which it does not.
[0042] In accordance with the present disclosure, novel microbial
inoculants and microbial fertilizer compositions are presented
which find application in increasing plant productivity and
improving soil quality. In particular embodiments the microbial
species present in the microbial inoculant or fertilizer
composition provide a symbiotic combination of organisms.
[0043] In the broadest embodiments, a microbial inoculant of the
present disclosure comprises strains of one or more bacterial
Lactobacillus species. The Lactobacillus species may be selected
from Lactobacillus parafarraginis, Lactobacillus buchneri,
Lactobacillus rapi and Lactobacillus zeae. The inoculant may
further comprise at least one Acetobacter species and at least one
Candida species.
[0044] The Lactobacillus parafarraginis strain may be Lactobacillus
parafarraginis Lp18. In a particular embodiment the Lactobacillus
parafarraginis strain is Lactobacillus parafarraginis Lp18
deposited with National Measurement Institute, Australia on 27 Oct.
2011 under Accession Number V11/022945. The Lactobacillus buchneri
strain may be Lactobacillus buchneri Lb23. In a particular
embodiment the Lactobacillus buchneri strain is Lactobacillus
buchneri Lb23 deposited with National Measurement Institute,
Australia on 27 Oct. 2011 under Accession Number V11/022946. The
Lactobacillus rapi strain may be Lactobacillus rapi Lr24. In a
particular embodiment the Lactobacillus rapi strain is
Lactobacillus rapi Lr24 deposited with National Measurement
Institute, Australia on 27 Oct. 2011 under Accession Number
V11/022947. The Lactobacillus zeae strain may be Lactobacillus zeae
Lz26. In a particular embodiment the Lactobacillus zeae strain is
Lactobacillus zeae Lz26 deposited with National Measurement
Institute, Australia on 27 Oct. 2011 under Accession Number
V11/022948.
[0045] The inoculant may further comprise a strain of Acetobacter
fabarum. The Acetobacter fabarum strain may be Acetobacter fabarum
Af15. In a particular embodiment the Acetobacter fabarum strain is
Acetobacter fabarum Af15 deposited with the National Measurement
Institute, Australia on 27 Oct. 2011 under Accession Number
V11/022943.
[0046] The inoculant may further comprise a yeast. The yeast may be
a strain of Candida ethanolica. The Candida ethanolica strain may
be Candida ethanolica Ce31. In a particular embodiment the Candida
ethanolica strain is Candida ethanolica Ce31 deposited with the
National Measurement Institute, Australia on 27 Oct. 2011 under
Accession Number V11/022944.
[0047] The concentrations of each microbial strain to be added to
microbial inoculants and fertilizer compositions as disclosed
herein will depend on a variety of factors including the identity
and number of individual strains employed, the plant species being
treated, the nature and condition of the soil to be treated, the
exact nature of the microbial inoculant or fertilizer composition
to be applied, the form in which the inoculant or fertilizer is
applied and the means by which it is applied, and the stage of the
plant growing season during which application takes place. For any
given case, appropriate concentrations may be determined by one of
ordinary skill in the art using only routine experimentation. By
way of example only, the concentration of each strain present in
the inoculant or fertilizer composition may be from about
1.times.10.sup.2 cfu/ml to about 1.times.10.sup.10 cfu/ml, and may
be about 1.times.10.sup.3 cfu/ml, about 2.5.times.10.sup.3 cfu/ml,
about 5.times.10.sup.3 cfu/ml, 1.times.10.sup.4 cfu/ml, about
2.5.times.10.sup.4 cfu/ml, about 5.times.10.sup.4 cfu/ml,
1.times.10.sup.3 cfu/ml, about 2.5.times.10.sup.3 cfu/ml, about
5.times.10.sup.3 cfu/ml, 1.times.10.sup.6 cfu/ml, about
2.5.times.10.sup.6 cfu/ml, about 5.times.10.sup.6 cfu/ml,
1.times.10.sup.7 cfu/ml, about 2.5.times.10.sup.7 cfu/ml, about
5.times.10.sup.7 cfu/ml, 1.times.10.sup.8 cfu/ml, about
2.5.times.10.sup.8 cfu/ml, about 5.times.10.sup.8 cfu/ml,
1.times.10.sup.9 cfu/ml, about 2.5.times.10.sup.9 cfu/ml, or about
5.times.10.sup.9 cfu/ml. In particular exemplary embodiments the
final concentration of the Lactobacillus strains is about
2.5.times.10.sup.5 cfu/ml, the final concentration of Acetobacter
fabarum may be about 1.times.10.sup.6 cfu/ml and the final
concentration of Candida ethanolica may be about 1.times.10.sup.5
cfu/ml.
[0048] Also contemplated by the present disclosure are variants of
the microbial strains described herein. As used herein, the term
"variant" refers to both naturally occurring and specifically
developed variants or mutants of the microbial strains disclosed
and exemplified herein. Variants may or may not have the same
identifying biological characteristics of the specific strains
exemplified herein, provided they share similar advantageous
properties in terms of promoting plant growth and providing
nutrients for plant growth in the soil. Illustrative examples of
suitable methods for preparing variants of the microbial strains
exemplified herein include, but are not limited to, gene
integration techniques such as those mediated by insertional
elements or transposons or by homologous recombination, other
recombinant DNA techniques for modifying, inserting, deleting,
activating or silencing genes, intraspecific protoplast fusion,
mutagenesis by irradiation with ultraviolet light or X-rays, or by
treatment with a chemical mutagen such as nitrosoguanidine,
methylmethane sulfonate, nitrogen mustard and the like, and
bacteriophage-mediated transduction. Suitable and applicable
methods are well known in the art and are described, for example,
in J. H. Miller, Experiments in Molecular Genetics, Cold Spring
Harbor Laboratory Press, Cold Spring Harbor, N.Y. (1972); J. H.
Miller, A Short Course in Bacterial Genetics, Cold Spring Harbor
Laboratory Press, Cold Spring Harbor, N.Y. (1992); and J. Sambrook,
D. Russell, Molecular Cloning: A Laboratory Manual, 3rd ed., Cold
Spring Harbor Laboratory Press, Cold Spring Harbor, N.Y. (2001),
inter alia.
[0049] Also encompassed by the term "variant" as used herein are
microbial strains phylogenetically closely related to strains
disclosed herein and strains possessing substantial sequence
identity with the strains disclosed herein at one or more
phylogenetically informative markers such as rRNA genes, elongation
and initiation factor genes, RNA polymerase subunit genes, DNA
gyrase genes, heat shock protein genes and recA genes. For example,
the 16S rRNA genes of a "variant" strain as contemplated herein may
share about 85%, 86%, 87%, 88%, 89%, 90%, 91%, 92%, 93%, 94%, 95%,
96%, 97%, 98% or 99% sequence identity with a strain disclosed
herein.
[0050] Microbial inoculants and fertilizer compositions of the
present disclosure may optionally further comprise one or more
additional microbial organisms, for example, additional
agronomically beneficial microorganisms. Such agronomically
beneficial microorganisms may act in synergy or concert with, or
otherwise cooperate with the organisms of the present disclosure in
the inoculant or fertilizer. Examples of agronomically beneficial
microorganisms include Bacillus sp., Pseudomonas sp., Rhizobium
sp., Azospirillum sp., Azotobacter sp., phototrophic and cellulose
degrading bacteria, Clostridium sp., Trichoderma sp. and the like.
Those skilled in the art will appreciate that this list is merely
exemplary only, and is not limited by reference to the specific
examples here provided.
[0051] In the soil environment, inoculated bacteria can find
survival difficult among naturally occurring competitor and
predator organisms. To aid in survival of microorganisms present in
microbial inoculants and fertilizer compositions of the present
disclosure upon application in the environment, one or more of the
strains may be encapsulated in, for example, a suitable polymeric
matrix. In one example, encapsulation may comprise alginate beads
such as has been described by Young et al, 2006, Encapsulation of
plant growth-promoting bacteria in alginate beads enriched with
humic acid, Biotechnology and Bioengineering 95:76-83, the
disclosure of which is incorporated herein by reference in its
entirety. Those skilled in the art will appreciate that any
suitable encapsulation material or matrix may be used.
Encapsulation may be achieved using methods and techniques known to
those skilled in the art. Encapsulated microorganisms can include
nutrients or other components of the inoculant or fertilizer
composition in addition to the microorganisms.
[0052] Those skilled in the art will appreciate that any plant may
benefit from the application of microbial inoculants and fertilizer
compositions of the present disclosure to soil, seeds and/or
vegetation. Particular embodiments are employed to aid the growth,
development, yield or productivity of crops and pastures or other
plants of economic value, including ornamentals and plants grown
for oils or biofuel. The crop plant may be, for example, a food
crop (for humans or other animals) such as any fruit, vegetable,
nut, seed or grain producing plant. Exemplary crop plants include,
but are not limited to, tubers and other below-ground vegetables
(such as potatoes, beetroots, radishes, carrots, onions, etc.),
ground-growing or vine vegetables (such as pumpkin and other
members of the squash family, beans, peas, asparagus, etc.), leaf
vegetables (such as lettuces, chard, spinach, alfalfa, etc.), other
vegetables (such as tomatoes, brassica including broccoli,
avocadoes, etc.), fruits (such as berries, olives, stone fruits
including nectarines and peaches, tropical fruits including mangoes
and bananas, apples, pears, mandarins, oranges, mandarins, kiwi
fruit, coconut, etc.), cereals (such as rice, maize, wheat, barley,
millet, oats, rye etc.), nuts (such as macadamia nuts, peanuts,
brazil nuts, hazel nuts, walnuts, almonds, etc.), and other
economically valuable crops and plants (such as sugar cane,
soybeans, sunflower, canola, sorghum, pastures, turf grass,
etc).
[0053] Microbial inoculants and fertilizer compositions of the
present disclosure may be applied directly to plants, plant parts
(such as foliage) or seeds, or alternatively may be applied to soil
in which the plants are growing or to be grown or in which seeds
have been or are to be sown. Application may be by any suitable
means and may be on any suitable scale. For example, application
may comprise pouring, spreading or spraying, including broad scale
or bulk spreading or spraying, soaking of seeds before planting,
and/or drenching of seeds after planting or seedlings. Those
skilled in the art will appreciate that multiple means of
application may be used in combination (for example soaking of
seeds prior to planting followed by drenching of planted seeds
and/or application to seedlings or mature plants). Seeds, seedlings
or mature plants may be treated as many times as appropriate. The
number of applications required can readily be determined by those
skilled in the art depending on, for example, the plant in
question, the stage of development of the plant at which treatment
is initiated, the state of health of the plant, the growth,
environmental and/or climatic conditions in which the plant is
grown and the purpose for which the plant is grown. For example, in
the case of flowering crops such as tomatoes, it may be desirable
to apply the microbial inoculant or fertilizer composition once or
more than once during the flowering period.
[0054] Thus, in accordance with the present disclosure, microbial
inoculants and fertilizer products as disclosed herein may be
prepared in any suitable form depending on the means by which the
inoculant or fertilizer composition is to be applied to the soil or
to plant seeds or vegetation. Suitable forms can include, for
example, slurries, liquids, and solid forms. Solid forms include
powders, granules, larger particulate forms and pellets. Solid form
fertilizer particles can be encapsulated in water soluble coatings
(for example dyed or undyed gelatin spheres or capsules), extended
release coatings, or by micro-encapsulation to a free flowing
powder using one or more of, for example, gelatin, polyvinyl
alcohol, ethylcellulose, cellulose acetate phthalate, or styrene
maleic anhydride. Liquids may include aqueous solutions and aqueous
suspensions, and emulsifiable concentrates.
[0055] In order to achieve effective dispersion, adhesion and/or
conservation or stability within the environment of inoculants and
fertilizer compositions disclosed herein, it may be advantageous to
formulate the inoculants and compositions with suitable carrier
components that aid dispersion, adhesion and
conservation/stability. Suitable carriers will be known to those
skilled in the art and include, for example, chitosan, vermiculite,
compost, talc, milk powder, gels and the like.
[0056] Additional components may be incorporated into inoculants
and fertilizer compositions of the present disclosure, such as
humic substances, trace elements, organic material, penetrants,
macronutrients, micronutrients and other soil and/or plant
additives.
[0057] Humus or humic substances that may be incorporated may
include, but are not limited to, humic acid derived from, for
example oxidised lignite or leonardite, fulvic acid and humates
such as potassium humate.
[0058] Organic material added may include, but is not limited to,
biosolids, animal manure, compost or composted organic byproducts,
activated sludge or processed animal or vegetable byproducts
(including blood meal, feather meal, cottonseed meal, ocean kelp
meal, seaweed extract, fish emulsions and fish meal).
[0059] Penetrants include, but are not limited to, non-ionic
wetting agents, detergent based surfactants, silicones, and/or
organo-silicones. Suitable penetrants will be known to those
skilled in the art, non-limiting examples including polymeric
polyoxyalkylenes, allinol, nonoxynol, octoxynol, oxycastrol,
TRITON, TWEEN, Sylgard 309, Silwet L-77, and Herbex
(silicone/surfactant blend).
[0060] Exemplary trace elements for inclusion in microbial
inoculants and fertilizer compositions are provided in Example 1.
However those skilled in the art will recognise that suitable trace
elements are not limited thereto, and that any trace elements
(natural or synthetic) may be employed.
[0061] Optional further soil and/or plant additives that can be
added to inoculants and fertilizer compositions of the present
disclosure include, for example, water trapping agents such as
zeolites, enzymes, plant growth hormones such as gibberellins, and
pest control agents such as acaracides, insecticides, fungicides
and nematocides.
[0062] The reference in this specification to any prior publication
(or information derived from it), or to any matter which is known,
is not, and should not be taken as an acknowledgment or admission
or any form of suggestion that that prior publication (or
information derived from it) or known matter forms part of the
common general knowledge in the field of endeavour to which this
specification relates.
[0063] The present disclosure will now be described with reference
to the following specific examples, which should not be construed
as in any way limiting the scope of the invention.
EXAMPLES
[0064] The following examples are illustrative of the invention and
should not be construed as limiting in any way the general nature
of the disclosure of the description throughout this
specification.
Example 1
Microbial Strains
[0065] The following microbial strains were used in the production
of a biofertilizer.
[0066] Lactobacillus parafarraginis Lp18 was isolated from an
environmental source. Partial 16S rRNA sequencing indicated 100%
similarity to Lactobacillus parafarraginis AB 262735 which has a
risk group of 1 (TRBA). When cultured on MRS media for 3 days at
34.degree. C., anaerobically, Lp18 produces cream, round, slight
sheen, convex, colony diameter 1-2 mm (facultative anaerobe). Its
microscopic appearance is Gram positive, non-motile, short rods
rectangular, mainly diploid. Lactobacillus parafarraginis Lp18 was
deposited with the National Measurement Institute, Australia on 27
Oct. 2011 under Accession Number V11/022945.
[0067] Lactobacillus buchneri Lb23 was isolated from an
environmental source. Partial 16S rRNA sequencing indicated 99%
similarity to Lactobacillus buchneri AB 429368 which has a risk
group of 1 (TRBA). When cultured on MRS media for 4 days at
34.degree. C., anaerobically, Lb23 produces cream, shiny, convex,
colony diameter 1-2 mm (facultative anaerobe). Its microscopic
appearance is Gram positive, non-motile, rods in chains.
Lactobacillus buchneri Lb23 was deposited with the National
Measurement Institute, Australia on 27 Oct. 2011 under Accession
Number V11/022946.
[0068] Lactobacillus rapi Lr24 was isolated from an environmental
source. Partial 16S rRNA sequencing indicated 99% similarity to
Lactobacillus rapi AB 366389 which has a risk group of 1 (DSMZ).
When cultured on MRS media for 4 days at 34.degree. C.,
anaerobically, Lr24 produces cream, round, shiny colonies with a
diameter of 0.5 mm (facultative anaerobe). Its microscopic
appearance is Gram positive, non-motile, short rods single or
diploid. Lactobacillus rapi Lr24 was deposited with the National
Measurement Institute, Australia on 27 Oct. 2011 under Accession
Number V11/022947.
[0069] Lactobacillus zeae Lz26 was isolated from an environmental
source. Partial 16S rRNA sequencing indicated 99% similarity to
Lactobacillus zeae AB 008213.1 which has a risk group of 1 (TRBA).
When cultured on MRS media for 48 hours at 34.degree. C.,
anaerobically, Lz26 produces white, round, shiny, convex, colonies
with a diameter of 1 mm (facultative anaerobe). Its microscopic
appearance is Gram positive, non-motile, short rods almost coccoid,
diploid and some chains. Lactobacillus zeae Lz26 was deposited with
the National Measurement Institute, Australia on 27 Oct. 2011 under
Accession Number V11/022948.
[0070] Acetobacter fabarum Af15 was isolated from an environmental
source. Partial 16S rRNA sequencing indicated 100% similarity to
Acetobacter fabarum AM 905849 which has a risk group of 1 (DSMZ).
When cultured on Malt extract media for 3 days at 34.degree. C.,
AF15 produces opaque, round, shiny, convex, colony diameter 1 mm
(aerobic). Its microscopic appearance is Gram negative, rods single
or diploid. Acetobacter fabarum Af15 was deposited with the
National Measurement Institute, Australia on 27 Oct. 2011 under
Accession Number V11/022943.
[0071] Candida ethanolica Ce31 was isolated from an environmental
source. Partial 16S rRNA sequencing indicated 89% similarity to
Candida ethanolica AB534618. When cultured on Malt extract media
for 2 days at 34.degree. C., Ce31 produces cream, flat, dull,
roundish, colony diameter 2-3 mm (aerobic). Its microscopic
appearance is budding, ovoid yeast. Candida ethanolica Ce31 was
deposited with the National Measurement Institute, Australia on 27
Oct. 2011 under Accession Number V11/022944.
[0072] Maintenance of Cultures
[0073] 30% glycerol stocks were made of each isolate and maintained
at -80.degree. C. for long-term culture storage. Short-term storage
of the cultures are maintained at 4.degree. C. on agar slopes (3
month storage) and on agar plates which are subcultured monthly. To
maintain the isolates original traits, a fresh plate is made from
the -80.degree. C. stock following three plate subcultures.
Inoculum and Growth Media
[0074] The Lactobacillus strains were grown with or without air (L.
rapi prefers anaerobic) either in MRS broth (Difco) or on MRS agar
plates depending on application. The cultures were routinely grown
for 2 days at a mesophilic temperature of 30-34.degree. C. The
Acetobacter and Ethanolica strains are grown aerobically either in
Malt extract broth (Oxoid) or on Malt extract agar plates depending
on application. The cultures are routinely grown for 2 days at a
mesophilic temperature of 30-34.degree. C.
[0075] Fermenter `Seed` Preparation
[0076] For individual strains, using a sterile nichrome wire a
single colony is removed from a fresh culture plate and transferred
to a universal bottle containing 15 mL of sterile media. The bottle
is securely placed in a shaking incubator set at 30.degree. C., 140
rpm for 48 hrs (L. rapi is not shaken). After incubation a cloudy
bacterial growth should be visible. `Seed` inoculation bottles are
stored at 4.degree. C. until required (maximum 1 week).
[0077] Typically a 5% bacterial inoculation is required for a
fermenter run. The stored 15 ml culture seed is added to a Schott
bottle containing a volume of sterile media which is 5% of the
total fermenter working volume. The culture is incubated and shaken
in the same way as the 15 ml seed. Large scale automatic fermenters
are used to grow pure cultures of each isolate. There is an
automatic feed of alkali, antifoam and glucose. Typically the
temperature is maintained at 30-34.degree. C., pH 5.5 but the
oxygen and agitation varies depending on the microorganism.
Sample Analysis
[0078] After each large scale culturing of an isolate a sample is
aseptically withdrawn and a viability count undertaken using 10
fold serial dilutions, performed in a laminar flow hood. A wet
slide is also prepared and purity observed using a phase contrast
microscope to double check for contaminants that may be present but
unable to grow on the culture media. After 48 hours the viability
plates are checked for a pure culture (same colony morphology) and
the colonies counted to produce a colony forming unit per ml
(cfu/ml) value. A Grams stain is also performed.
Example 2
Pasture Trials
[0079] Field trials on pasture were conducted using a biofertlizer
as disclosed herein, in comparison to untreated pasture and pasture
treated with conventional inorganic fertilizers.
[0080] The biofertilizer (hereinafter "IMP Bio") comprised the six
microbial strains listed in Example 1, at final concentrations of
2.5.times.10.sup.5 cfu/ml for each of the Lactobacillus strains,
1.0.times.10.sup.5 cfu/ml for Candida ethanolica and
1.0.times.10.sup.6 cfu/ml for Acetobacter fabarum. The strains were
grown as described in Example 1 and mixed with 2% trace elements,
0.3% humate (Soluble Humate, Lawrie Co), 3% molasses and 0.1-0.2%
phosphoric acid. Phosphoric acid was added to the point where pH
was in the range 3.8 to 4.0. The trace elements component typically
comprised the following (per 1,000 L):
TABLE-US-00001 TABLE 1 Trace elements component of biofertilizer
Material Volume (kg) Water 200 kg Potassium Sulphate 15.25 kg
Copper Complex.sup.1 25.6 kg Magnesium Citrate.sup.2 175.0 kg
Chromium Citrate.sup.3 10.0 kg Calcium Sokolate.sup.4 52.0 kg
Citric Acid 11.15 kg Ferrous Sulphate 4.0 kg Cobalt Sulphate 750 g
Nickel Sulphate 250 g Manganese Sulphate 4.0 kg Urea 31.0 kg Zinc
Sulphate 4.0 kg Borax 4.5 kg M A P 13.25 kg Sodium Molybdate 2.5 kg
Acetic Acid 10.8 kg Sugar 50.0 kg
[0081] Conventional inorganic fertilizers used as comparators were
Spray Gro Liquid, Urea, DAP (diammonium phosphate), and 14:16:11
commercial NPK mix.
[0082] Sites for the pasture trials were selected based on rainfall
levels, soil type, pasture composition and past fertilizing
practices. The following locations in Tasmania were used: Nabageena
(high rainfall; rye grass, cocksfoot, Yorkshire fog and other
grasses), Cuprona (high rainfall; rye grass), West Moorville/Upper
Burnie (high rainfall; rye grass), Connorville (dryland pasture;
degraded) and Connorville (irrigated pasture; rye grass).
[0083] At each location, multiple 4.times.10 m strips of pasture
were prepared by mowing to a height of 45 mm (and removal of
clipped plant material prior to fertilizing). At West
Moorville/Upper Burnie and Nabageena, IMP Bio was applied to
replicate plots at 20 L/ha, 30 L/ha or 50 L/ha, and 14:16:11 NPK
mix was applied to replicate plots at 250 kg/ha. At West Moorville,
DAP was also applied to replicate plots at 125 kg/ha. At Cuprona,
IMP Bio was applied to replicate plots at 20 L/ha, 30 L/ha or 50
L/ha, and Spray Gro Liquid Urea was applied at 50 L/ha. At
Connorville, IMP Bio was applied to replicate plots at 20 L/ha, 30
L/ha or 50 L/ha, and DAP was applied to replicate plots at 125
kg/ha. IMP Bio and SprayGro Urea were applied as large droplets
through 2 m backpack boom sprays in a single pass. 14:16:11 NPK mix
and DAP were applied by hand distribution. At each location,
replicate control (unfertilized) plots were set aside.
[0084] Plant yield and leaf nutrient content were analysed 6-8
weeks after treatment.
[0085] Results for plant yield are shown in Table 2 below. These
results indicate that the IMP Bio fertilizer produced yields at
least similar to, and in some cases superior to, conventional
inorganic fertilizers.
TABLE-US-00002 TABLE 2 Yield (kg/ha/day) Conventional IMP Bio IMP
Bio (half Area Control fertilizer (30 L/ha) strength) Cuprona 65 79
(Spray Gro) 75 -- Nabageena 60 78 (14:16:11) 73 -- Connorville 35
34 (DAP) 32 31 (dryland) Connorville 44 56 (DAP) 51 44 (irrigated)
West Moorville 67 90 (DAP) 87 --
[0086] Plant material nutrient analysis was conducted, as shown in
Table 3 below. Key elements required by, or beneficial to, the
pasture for growth (such as nitrogen, phosphorous, potassium,
calcium, copper, zinc, boron, molybdenum) were present in plant
material from the IMP Bio treated plots at levels equivalent to or
higher than those plots treated with the comparator conventional
inorganic fertilizer, despite these nutrients not being added in
the IMP Bio fertilizer.
TABLE-US-00003 TABLE 3 Conventional IMP Bio Nutrient Control
fertilizer (30 L/ha) Connorville (irrigated) Nitrogen (%) 1.95 2.23
1.94 Phosphorus (%) 0.28 0.38 0.26 Potassium (%) 2.61 2.69 2.53
Sulphur (%) 0.26 0.27 0.24 Carbon (%) 43.5 43.7 43.8 Calcium (%)
0.33 0.30 0.41 Magnesium (%) 0.28 0.25 0.28 Sodium (%) 0.24 0.45
0.30 Copper (ppm) 4.2 4.5 5.3 Zinc (ppm) 19 21 24 Manganese (ppm)
372 339 309 Iron (ppm) 113 90 109 Boron (ppm) 4.9 4.7 6.0
Molybdenum (ppm) 0.7 0.7 0.7 Cobalt (ppm) 0.2 0.1 0.2 Silicon (ppm)
201 169 193 Nitrogen:Sulphur ratio 7.4 8.4 8.1 Nitrogen:Phopshorus
ratio 7.0 5.9 7.4 Nitrogen:Potassium ratio 0.7 0.8 0.8
Carbon:Nitrogen ratio 22.3 19.6 22.6 Crude protein (% N .times.
6.25) 12.2 13.9 12.1 West Moorville Nitrogen (%) 1.56 1.57 1.64
Phosphorus (%) 0.34 0.33 0.31 Potassium (%) 2.26 2.43 2.11 Sulphur
(%) 0.25 0.24 0.24 Carbon (%) 44.0 44.1 43.9 Calcium (%) 0.78 0.59
0.57 Magnesium (%) 0.24 0.20 0.18 Sodium (%) 0.18 0.14 0.15 Copper
(ppm) 4.8 4.3 4.7 Zinc (ppm) 18 18 19 Manganese (ppm) 37 33 35 Iron
(ppm) 172 114 120 Boron (ppm) 10 7.7 8.3 Molybdenum (ppm) 1.3 1.0
1.1 Cobalt (ppm) 0.1 <0.1 <0.1 Silicon (ppm) 316 268 244
Nitrogen:Sulphur ratio 6.2 6.5 7.0 Nitrogen:Phosphorus ratio 4.5
4.7 5.3 Nitrogen:Potassium ratio 0.7 0.6 0.8 Carbon:Nitrogen ratio
28.2 28.1 26.8 Crude protein (% N .times. 6.25) 9.8 9.8 10.2
Cuprona Nitrogen (%) 3.68 3.60 3.68 Phosphorus (%) 0.39 0.38 0.39
Potassium (%) 3.43 3.43 2.90 Sulphur (%) 0.38 0.41 0.41 Carbon (%)
43.6 44.2 43.6 Calcium (%) 0.51 0.49 0.58 Magnesium (%) 0.24 0.27
0.26 Sodium (%) 0.26 0.36 0.44 Copper (ppm) 8.7 9.1 8.4 Zinc (ppm)
24 25 22 Manganese (ppm) 106 118 74 Iron (ppm) 104 110 103 Boron
(ppm) 6.2 4.2 4.4 Molybdenum (ppm) 0.3 0.3 0.9 Cobalt (ppm) <0.1
<0.1 <0.1 Silicon (ppm) 267 284 214 Nitrogen:Sulphur ratio
9.8 8.8 9.1 Nitrogen:Phopshorus ratio 9.5 9.5 9.3
Nitrogen:Potassium ratio 1.1 1.1 1.3 Carbon:Nitrogen ratio 11.8
12.3 11.9 Crude protein (% N .times. 6.25) 23.0 22.5 23.0
Example 3
Soil Quality
[0087] To determine the effect of a biofertilizer as disclosed
herein on soil quality, 2.times.150 g of soil from a farm in
Tasmania were each weighed into 2.times. clean 150 ml Schott
bottle. 10 mls of a 1:10 dilution of IMP Bio fertilizer (see
Examples 1 and 2) was dripped over the top of the soil in one
bottle and the lid replaced and incubated at 34.degree. C. for one
week. The second bottle had no biofertilizer added was incubated
34.degree. C. The soil from both bottles was analysed by
Environmental Analytical Laboratories (EAL, Southern Cross
University Lismore, NSW) using standard soil testing methods.
[0088] The results for the one week treatment of soil with IMP Bio
are summarised in Table 4. Soil tests on the untreated incubated
sample are not shown as these were substantially the same as the
initial untreated soil test. It is clear from the soil tests on the
two treated samples that there is a marked difference in the soil
after incubation with IMP Bio. The second sample analysed, shows a
general trend of increasing the levels of available cations
(calcium, magnesium, potassium, sodium and all trace
elements--zinc, manganese, iron and copper) and ammonium nitrogen,
while the total levels under the acid extractions were slightly
lower across all nutrients. Organic matter increased by 1% (14.6%
to 15.5%) between the samples dates. The overall decrease in total
nutrients does not appear to be significant.
[0089] There was a greater than three-fold increase in ammonium
nitrogen, although no increase in nitrates. This indicates an
increase in mineralisation of nitrogen from the organic nitrogen
pool, and may be linked to the transformation of organic material,
the level of which in this soil is particularly high. This could
also indicate nitrogen fixation.
TABLE-US-00004 TABLE 4 Prior to IMP Bio After IMP Bio Nutrient/soil
characteristic treatment treatment Calcium (mg/kg) 1006 1431
Magnesium (mg/kg) 181 279 Potassium (mg/kg) 218 317 Phosphorus
(mg/kg) 2.2 3.3 Nitrate nitrogen (mg/kg) 13.3 14.2 Ammonium
nitrogen (mg/kg) 21.2 72.6 Sulfur (mg/kg) 28.5 33.8 Zinc (mg/kg)
3.0 3.6 Manganese (mg/kg) 19 48 Iron (mg/kg) 335 369 Copper (mg/kg)
3.4 3.5 Boron (mg/kg) 0.82 0.98 Silicon (mg/kg) 24 28 Total carbon
(%) 8.33 8.85 Total nitrogen (%) 0.52 0.53 Carbon:Nitrogen ratio
16.1 16.6 Organic matter (%) 14.6 15.5 pH 6.41 6.36 Conductivity
(dS/m) 0.132 0.202
Example 4
Potato Trials
[0090] A field trial was conducted in which Bondi variety potatoes
were treated with the IMP Bio biofertilizer (see Example, 2) at
planting. The trial was conducted at Waterhouse, Tasmania. IMP Bio
was applied in furrows to rows 30 m long at a rate of 50 L/ha,
either alone, or together with the conventional chemical fertilizer
5-10-16 at either 650 kg/ha (delivering 32 kg/ha nitrogen, 63 kg/ha
phosphorus and 100 kg/ha potassium) or 1250 kg/ha (delivering 63
kg/ha nitrogen, 125 kg/ha phosphorus and 200 kg/ha potassium). In a
fourth replicate, 5-10-16 was applied at 12504/ha together with the
fungicide Amistar. Four plots of 4 m length were dug from each
treatment and tubers assessed for size and yield. The results are
shown in Table 5.
TABLE-US-00005 TABLE 5 Potato yield Yield Yield Total yield >350
g <45 g Stems/ Treatment >45 g (t/ha) Seed (t/ha) (t/ha)
(t/ha) plant IMP Bio 42.4 38.1 4.3 2.9 3.7 IMP Bio + 5-10- 39.2
35.4 3.8 1.7 3.3 16 (650 kg/ha) IMP Bio + 5-10- 35.6 30.0 5.6 1.6
3.3 16 (1250 kg/ha) 5-10-16 + Amistar 39.3 33.4 5.9 1.8 3.2
[0091] There was an increase in stem numbers per plant in the IMP
Bio treatment, which is desirable (higher stem numbers typically
correlating with higher tuber numbers). The reduction in large
(>350 g) tubers observed with IMP Bio treatment is also
significant as larger tubers have lower commercial value than seed
sized tubers (45-350 g). Additionally, the 14% increase (5
tonnes/ha) in seed weight in the IMP Bio compared to the
5-10-16+Amistar treatment is also of significant economic value.
The IMP Bio treated potato plants were also observed to be
approximately three weeks more developed (in terms of maturity)
than those treated with 5-10-16.
Example 5
Tick Bean Trials
[0092] A greenhouse experiment was conducted to establish the
effect of IMP Bio biofertilizer (see Example 2) on tick bean plant
growth, compared to the commercial fertilizer Baileys TriStar (8.3%
N, 0% P, 16% K, 14% S, 1% Fe, 2% Mg).
[0093] The treatment groups and regimes employed for seedlings
post-germination were as follows:
Control: 300 .mu.l water
"T40": 300 .mu.l TriStar at 40 L/Ha
"SGL40": 300 .mu.l IMP Bio at 40 L/ha
[0094] "T25% GL40": 300 .mu.l TriStar 25% plus IMP Bio at 40
L/ha
"GL40": 300 .mu.l IMP Bio at 40 L/ha
[0095] Seeds in the T40, SGL40 and T25% GL40 groups were soaked for
1 hour in 100 ml of a 1:10 dilution of IMP Bio solution prior to
planting. Control and GL40 seeds remained dry prior to planting.
Three replicates of each treatment group (and two replicates of the
control group) were used. Seeds were planted 5 mm deep in the
middle of each pot and the pots placed in a temperature-controlled
greenhouse at 16-18.degree. C. under hydroponic lights. After
germination, all seedlings were treated every two weeks (for a
total of four weeks) using the treatments described above.
Seedlings were watered once a day.
[0096] At the conclusion of the experiment it was observed that the
tallest plants, and the plants with the strongest main stem were
those of the T25% GL40 treatment group. Overall, the best growth
was observed in the T25% GL40 and SGL40 groups (data not shown).
However the most noticeable differences observed were in root
development (see FIG. 1). Roots of the control plants were the
least dense and the shortest (FIG. 1A). Roots of the T40 plants had
good root density and length (FIG. 1B), however development was not
as extensive as in the plants treated with IMP Bio. In the SGL40
plants the root system shown good density and length (FIG. 1C).
Root nodules were present as were black nodule-like growths. In the
T25% GL40 plants the root system was more dense and longer than in
other treatment groups (FIG. 1D). Root nodules were present but
black nodule-like growth was not seen. In the GL40 plants the root
system was similarly dense, long and well developed (FIG. 1E). Root
nodules were present as were black nodule-like growths.
Example 6
Tomato Trials
[0097] A greenhouse experiment was conducted to investigate the
effect of IMP Bio biofertilizer (see Example 2) on the growth rate
of tomato plants over a 20 day period. Tomato seedlings were
provided by Cedenco. Water only was used as a control, and the
commercial fertilizer FlowPhos (Yara Nipro) used as a comparator.
Seedlings were potted into 50 mm pots in one of three different
soils obtained from different locations (Cedenco) and drenched once
with either: (i) 10 ml water; (ii) 10 ml of IMP Bio (100 ml in 900
ml water); (iii) 10 ml of FlowPhos (7.5 ml in 900 ml water); or
(iv) 10 ml of FlowPhos plus IMP Bio (7.5 ml FlowPhos and 100 ml IMP
Bio made to a total volume of 1000 ml with water). Three replicates
of the control (water) group and eight replicates of each of the
treatment groups. Plants were watered twice a day with 30 ml water.
Plant height was measured every third day over the 20 day period of
the experiment.
[0098] The average rate of change of growth (height) of tomato
seedlings over the 20 day period for all treatment groups, in each
of the three soils, is shown in FIG. 2. As can be seen, the IMP Bio
treated plants were the only plants that consistently showed
increases in growth over the course of the experiment, resulting in
taller plants. FIG. 3 shows an exemplary comparison of difference
in plant height, foliage and root system development in control
plants, FlowPhos treated plants and IMP Bio (GreatLand) treated
plants, in which the advantages of IMP Bio treatment are clearly
evident.
[0099] A field trial was then conducted at Timmering, Victoria in
which tomato plants were treated with IMP Bio by foliar application
during flowering, either at a rate of 80 L/ha or 40 L/ha during
early flowering followed by 40 L/ha during mid flowering. Yield of
tomato fruit was determined and compared to the yield from the same
number of untreated plants. For the plants that received 80 L/ha
IMP Bio, total fruit yield was 149.87 tonnes/ha, compared to 128.87
tonnes/ha for the untreated plants. For the plants that received
two applications of 40 L/ha IMP Bio, total fruit yield was 130.15
tonnes/ha, compared to 103.05 tonnes/ha for the untreated
plants.
Example 7
Macadamia Trials
[0100] A field trial was conducted in which macadamia trees in a
100 ha farm in Lismore, NSW were treated with the IMP Bio
biofertilizer (see Example 2) by spraying at the rate of 40 L/ha,
every 2-3 months for a period of 12 months. IMP Bio was applied in
conjunction with chemical fertilizer (Easy N Fertilizer), the same
fertilizer used for at least the previous four years. The yield of
macadamia nuts following the 12 month treatment was approximately
70 tonnes, compared to an average yield of 35 tonnes per year over
the previous four years. The benefits offered by the IMP Bio
biofertilizer allowed for a significant reduction in the
application of chemical fertilizer.
[0101] Leaf and soil analysis was also conducted at four sites
across the farm after 45 days of IMP Bio use. Significant increases
were observed in levels of zinc, manganese, iron and boron in
macadamia leaves, and in ammonium nitrogen, nitrate nitrogen,
phosphorus, potassium, calcium, copper and boron in the soil.
Example 8
Strawberry Trials
[0102] A field trial was conducted in Beerwah, Qld to establish the
effect of IMP Bio biofertilizer (see Example 2) on strawberry plant
growth and fruit yield over an 8 ha plot. The IMP Bio was applied
at a rate of 40 L/ha to the soil pre-planting, again at the same
rate at planting, and weekly during the vegetative growth and
flowering stage (weeks 2-4), during the fruiting stage (weeks 5-8)
and during the picking stage (weeks 9-16). In comparison to
conventional fertilizer (NitroPhoska(blue) applied preplanting at
1000 kg/ha), plant growth rate was significantly increased and
plants showed increased vegetative growth and leaf area (FIG. 4).
Fruit yield was also significantly increased (38,000 kg as compared
to 20,000 kg).
Example 9
Other Trials
[0103] Preliminary trials have also been conducted on sugar cane,
lettuce, raspberries, roses, wheat, basil and turf grass (golf
course green). In each case IMP Bio biofertilizer (see Example 2)
was observed to result in increased rate of growth of plants
compared to untreated plants (data not shown).
* * * * *