Benefits[edit]
- These are means of fixing the nutrient availability in the soil.
- Since a bio-fertilizer is technically living, it can symbiotically associate with plant roots. Involved microorganisms could readily and safely convert complex organic material into simple compounds, so that they are easily taken up by the plants. Microorganism function is in long duration, causing improvement of the soil fertility. It maintains the natural habitat of the soil. It increases crop yield by 20-30%, replaces chemical nitrogen and phosphorus by 30%, and stimulates plant growth. It can also provide protection against drought and some soil-borne diseases.
- Azolla-Anabena symbiosis: Azolla is a small, eukaryotic, aquatic fern having global distribution.Prokaryotic blue green algae Anabena azolla resides in its leaves as a symbiont. Azolla is an alternative nitrogen source. This association has gained wide interest because of its potential use as an alternative to chemical fertilizers.
- Rhizobium: Symbiotic nitrogen fixation by Rhizobium with legumes contribute substantially to total nitrogen fixation. Rhizobium inoculation is a well-known agronomic practice to ensure adequate nitrogen
Types of biofertilizers
Nitrogen Biofertilizers
Phosphorus Biofertilizers
Compost Biofertilizers
- symbiotic nitrogen fixers, Rhizobium spp.;
- non-symbiotic, free-living nitrogen fixers (Azotobacter, Azospirillum, etc.);
- algal biofertilizers (blue-green algae or blue-green algae in association with Azolla);
- phosphate-solubilising bacteria;
- mycorrhizae;
- organic fertilizers.
- Nitrogen-fixing biofertilizers Nitrogen-fixing bacteria function under two types of conditions, symbiotically and as free-living (non-symbiotic) as well as associative symbiotic bacteria.
- Absorption of water,
- Solubilisation of organic matter of the soil humus, release of inorganic nutrients, absorption and their transfer to root,
- Direct absorption of minerals from the soil over a large area and handing over the same to the root. Plants with ectomycorrhiza are known to absorb 2–3 times more of nitrogen, phosphorus, potassium and calcium,
- The fungus secretes antimicrobial substances which protect the young roots from attack of pathogens. Ectomycorrhiza occurs in trees such as Eucalyptus, oak (Quercus), peach, pine, etc. The fungus partner is generally specific. It belongs to Basidiomycetes.
- Make nutrients available.
- Make the root rhizosphere livelier.
- Growth-promoting substances are produced.
- More root proliferation.
- Better germination.
- Improve the quality and quantity of produce.
- Improve the fertilizer use efficiency.
- Higher biotic and abiotic stress tolerance.
- Improve soil health.
- Residual effect.
- Make the system more sustainable.
Liquid Biofertilizers
Benefits:
- Longer shelf-life – 12–24 months;
- No contamination;
- No loss of properties due to storage up to 45º C;
- Greater potential to fight with native population;
- Easy identification by typical fermented smell;
- Better survival on seeds and soil;
- Very easy to use by the farmer;
- High commercial revenues;
- High export potential.
- Dull white in colour;
- No bad smell;
- No foam formation, pH 6.8–7.5
- The colour of the liquid may be blue or dull white.
- Bad odour confirms improper liquid formulation and may be considered as mere broth.
- Production of yellow gummy colour materials confirms the quality product.
- Acidic pH always confirms that there are no Azospirillum bacteria in the liquid.
- Stimulates growth and imparts green colour which is a characteristic of a healthy plant.
- Aids utilization of potash, phosphorous and other nutrients.
- Enhances the plumpness and succulence of fruits and increases the protein content.
- Produces brown-black pigmentation in liquid inoculum;
- Produces yellow-light brown pigmentation in liquid inoculum;
- Produces green fluorescent pigmentation in liquid inoculum;
- Produces green fluorescent pigmentation in liquid inoculum;
- Produces, pink pigmentation in liquid inoculum;
- Produces less, gum-less, greyish-blue pigmentation in liquid inoculum;
- Produces green-fluorescent pigmentation in liquid inoculum.Acetobacter
Carrier-based | Liquid-based |
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Cheap | Longer shelf-life |
Easier to produce | Easier to produce |
Less investment | Temperature tolerant |
High cell counts | |
Contamination-free | |
More effective | |
Product can be 100% sterile | |
Disadvantages | |
Low shelf-life | High cost |
Temperature sensitive | Higher investment for production unit |
Contamination prone | |
Low cell counts | |
Less effective | |
Automation difficult |
VIDEO OF THE DAY
Affordability
Improved Soil
Improved Plants
Disadvantages
Biofertilizers
Types of Biofertilizers:
- Bacteria
- Fungi
- Cyanobacteria
Bacteria
Fungi
- Tolerance to drought conditions and salinity.
- Resistance to root-borne pathogens.
- An overall increase in plant growth and development.
Cyanobacteria
Solved Example For You
- Oscillatoria
- Rhizobium
- Nostoc
- Mycorrhizae
Biofertilizer Mycorrhiza as Biofertilizers
In recent years, use of artificially produced inoculum of mycorrhizal fungi has increased its significance due to its multifarous role in plant growth and yield, and resistance against climatic and edaphic stresses, pathogens and pests.
Mechanism of Symbiosis
The mechanism of symbiosis is not fully understood. Biorkman (1949) postulated the carbohydrate theory and explained the development of mycorrhizas in soils deficient in available P and N, and high light intensity. Slankis (1961) found that at high light intensity, surplus carbohydrates are formed which are exuded from roots. This in turn induces the mycorrhizal fungi of soil to infect the roots. At low light intensity, carbohydrates are not produced in surplus, therefore, plant roots fail to develop mycorrhizas. Types of Mycorrhizas
By earlier mycologists the mycorrhizas were divided into the following three groups :
(i) Ectomycorrhiza. It is found among gymnosperms and angiosperms. In short roots of higher plants generally root hairs are absent. Therefore, the roots are infected by mycorrhizal fungi which, in turn, replace the root hairs (if present) and form a mantle. The hyphae grow intercellularly and develop Hartig net in cortex. Thus, a bridge is established between the soil and root through the mycelia.
(ii) Endomycorrhiza. The morphology of endomycorrhizal roots, after infection and establishment, remain unchanged. Root hairs develop in a normal way. The fungi are present on root surface individually. They also penetrate the cortical cells and get established intracellulary by secreting extracellular enzymes. Endomycorrhizas are found in all groups of plant kingdom.
(iii) Ectendomycorrhiza. In the roots of some of the gymnosperms and angiosperms, ectotrophic fungal infection occur. Hyphae are established intracellularly in cortical cells. Thus, symbiotic relation develops similar to ecto- and endo-mycorrhizas.
Marks (1991) classified the mycorrhizas into seven types on the basis of types of relationships with the hosts (i) vesicular-arbuscular (VA) mycorrhizas (coiled, intracellular hyphae, vesicle and arbuscules present), (ii) ectomycprrhizas (sheath and inter-cellular hyphae present), (iii) ectendomycorrhizas (sheath optional, inter and intra-cellular hyphae present), (iv) arbutoid mycorrhizas (seath, inter-and coiled intracellular hyphae present), (v) monotropoid mycorrhizas (sheath, inter- and intra- cellular hyphae and peg like haustoria present), (vi) ericoid mycorrhizas (only coiled intracellular hyphae, long coiled hyphae present), and (viii) orchidaceous mycorrhizas (only coiled intracellujlar hyphae present). Type (i) is present in all groups of plant kingdom; Types (ii) and (iii) are found in gymnosperms and angiosperms. Types (iv), (v)and (vi) are restricted to Ericales, Monotropaceae and Ericales respectively. Types (vii)is restricted to Orchidaceous only. Types (iv) and (v) were previously grouped under ericoid mycorrhizaes.
Methods of Inoculum Production and Inoculation
Methods of inoculum production of VAM fungi differ; however, some of these two are briefly described here.
(a) Ectomycorrhizal fungi: The basidiospores, chopped sporocarp, sclerotia, pure mycelia culture, fragmented mycorrhizal roots or soil from mycorrhizosphere region can be used as inoculum. The inoculum is mixed with nursery soils and seeds are sown.
Institute for Mycorrhizal Research and Development, U.S.A., Athens and Abbort Laboratories (U.S.A) have developed a mycelial inoculum of Pisolithus tinctorius in a vermiculite-peat moss substrate with a trade name ‘Myco-Rhiz’ which is now commercially available on large quantities. In 1982, about 1.5 million pine seedlings were produced with MycoRhiz in the U.S.A. (Marx and Schenck, 1983).
(b) VA mycorrhizal fungi : VA mycorrhizas can be produced on a large scale by pot culture technique. This requires the host plants, mycorrhizal fungi and natural soil. The host plants which support large scale production of inoculum are sudan grass, strawberry, sorghum, maize, onion, citrus, etc.
The starter inoculum (spores) of VA mycorrhizal fungi can be isolated from soil by wet sieving and decantation technique (Gerdeman and Nicolson, 1963). VA mycorrhizal spores are surface sterilized and brought to the pot culture. Commonly used pot substrates are sand: soil (1:1, w/w) with a little amount of moisture. An out line for inoculum production is given in Fig. 12.5.
There are two methods of using the inoculum : (i) using a dried spore-root- soil to plants by placing the inoculum several centimeters below the seeds or seedlings, (ii) using a mixture of soil-roots, and spores in soil pellets and spores adhered to seeds with adhesives.
Commercially available pot culture of VA mycorrhizal hosts grown under aseptic conditions can provide effective inoculum. Various types of VA mycorrhizal inocula are currently produced by Native Plants, Inc (NPI), Salt Lake City.
In India, Forest Research Institute, Dehra Dun has established mycorrhizal bank in different states of the country. Inocula of these can be procured as needed and used in horticulture and forestry programmes.
Benefits from Mycorrhizas to Plants
i) | They increase the longevity of feeder roots, surface area of roots by forming mantle and spreading mycelia into soil and, in turn, the rate of absorption of major and minor nutrients from soil resulting in enhanced plant growth. |
(ii) | They play a key role for selective absorption of immobile (P, Zn and Cu) and mobile (S, Ca, K, Fe, Mn, Cl, Br, and N) elements to plants. These are available to plants in less amount (Tinker, 1984). |
(iii) | Some of the trees like pines cannot grow in new areas unless soil has mycorrhizal inocula because of limited or coarse root hairs. |
(iv) | VA mycorrhizal fungi enhance water uptake in plants, |
(v) | VA mycorrhizal fungi reduce plant response to soil stress such as high salt levels, toxicity associated with heavy metals, mine spoils, drought and minor element (e.g. Mn) imbalance. |
(vi) | VA mycorrhizal fungi decrease transplant socks to seedlings. They produce organic 'glues' which bind soil particles into semistable in aggregates. Thus, they play a significant role in augmenting soil fertility and plant nutrition. |
(vii) | Some of them produce metabolites which change the ability of plants to induce roots from woody plant cuttings and increase root development during vegetative propagation. |
(viii) | They increase resistance in plants and with their presence reduce the effects of pathogens and pests on plant health. |
About VAM
. No. | Groups | Examples |
N2 fixing Biofertilizers
| ||
1. | Free-living | Azotobacter, Beijerinkia, Clostridium, Klebsiella, Anabaena, Nostoc, |
2. | Symbiotic | Rhizobium, Frankia, Anabaena azollae |
3. | Associative Symbiotic | Azospirillum |
P Solubilizing Biofertilizers
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1. | Bacteria | Bacillus megaterium var. phosphaticum, Bacillus subtilis Bacillus circulans, Pseudomonas striata |
2. | Fungi | Penicillium sp, Aspergillus awamori |
P Mobilizing Biofertilizers
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1. | Arbuscular mycorrhiza | Glomus sp.,Gigaspora sp.,Acaulospora sp., Scutellospora sp. & Sclerocystis sp. |
2. | Ectomycorrhiza | Laccaria sp., Pisolithus sp., Boletus sp., Amanita sp. |
3. | Ericoid mycorrhizae | Pezizella ericae |
4. | Orchid mycorrhiza | Rhizoctonia solani |
Biofertilizers for Micro nutrients
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1.
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Silicate and Zinc solubilizers
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Bacillus sp.
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Plant Growth Promoting Rhizobacteria
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1.
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Pseudomonas
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Pseudomonas fluorescens
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- Bio-Fertilizers are supplement to Chemical Fertilizers.
- Bio-Fertilizers are cheap and can reduce the cost of cultivation.
- Fix Biological Nitrogen in the soil, which is readily available to the plant.
- Increase crop yield by 4-5% on an average.
- Improve soil properties and sustain soil fertility.
- Provides plant nutrient at low cost and useful for the consecutive crops.
Name of Bio-Fertilizers | Contribution | Most Beneficiary Crop |
A. NitrogenBio-Fertilizer 1.Rhizobium(Symbiotic) | a) Fixes 50-300 Kg. N/hactre b) Leaves residual nitrogen for succeeding crop. c) Increase yield by 10-35% d) Maintains soil fertility. |
Pulse Legumes : Gram, Peas, Lentil, Moong, Urd, Cowpea, Arhar. Oil
Legumes : Groundnut and Soyabeans. Fodder Legumes : Barseem, Lucerne. Forest Legumes : Subabul, Shisam, Shinsh. |
2. Azetobactor (Non-Symbiotic) |
a) Fixes 20-40 mgN/g of C-Source
b) Produces growth promoting substances like vitamin B groups, Indole acetic acid and Giberellic acid. c) 0-15% increase in yield. d) Maintains soil fertility. e) Biological control of plant diseases by suppressing some plant pathogens. |
Wheat, Jowar, Barley, Maize, Paddy, Mustard, Sunflower, Sesamum. Cotton, Sugarcane, Banana, Grapes, Papaya,Watermelon, Onion, Potato, Tomato, Cauliflower, Chilly, Lady finger, Rapeseed, Linseed, Tobacco. Mulberry, Coconut, Spices, Fruits, Flowers. Plantation crops, Forest plants
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B) Phosphorous
Bio-fertilizer 1. P.S.B. Phosphate solubilising Bacteria |
a) Solublizes insoluble
phosphate. b) Increases yield by 10-30%. c) Produce enzymes which mineralise organic phosphorous to a solubleform. |
Non-specific : All Plants.
|
What is the difference between Organic fertilizer and Bio-fertilizers?
Bio-organic fertilizer, which is finished organic fertilizer, is purified by means of physical methods to reduce the moisture of manure. Today, so many organic fertilizer plants are also can produce bio organic fertilizer with same fertilizer production line. Bio-organic fertilizer is the fertilizer with the function of both microbial fertilizer and organic fertilizer. with animal and plant residues (such as manure, straw, etc.) as the raw materials and special funtional microbes, by sound processing and decomposition, finished appearance (sensory) for the product should be loose powder, no bad smell; particulate product should be no mechanical impurities, uniform size, taste-free.Require the use of microbial strains should be safe, effective, and there is a clear source of Species.The difference between the two:First, the presence or absence of microorganisms. Bio-organic fertilizer contains a variety of beneficial microorganisms inside, but all microorganisms in organic fertilizer after high temperature treatment substantially are killed, which is difficult to provide beneficial soil microbes.Second, different nutrients. Organic fertilizer through high-temperature treatment, nutrient losses during treatment of high temperature.Third, different odors. Organic fertilizer by drying, deodorizing effect of organic fertilizer is not ideal because of drying treatment. once organic fertilizer is damp, stench is issued. Bio-organic fertilizer fundamentally eliminate the odor, because it can turn uric acid into the urine bacterial protein.Item Index of organic fertilizer technical indicatorsOrganic matter content (dry basis), ≥45%Total nutrient (N + P2O5 + K2O) content (dry basis), ≥5.0%Moisture (free water) content, ≤30%PH pH 5.5-8.0Heavy metal content, Ascaris eggs and E. coli mortality value indicators in organic fertilizer should be normal by governmental requirements.Technical requirements for bio-organic fertilizerItem IndexThe effective number of viable cells (cfu), ≥ 0.20 g/ one hundred millionOrganic matter (dry basis), ≥ 40.0%Moisture, ≤ 30.0%pH value of 5.5 to 8.5Fecal coliform, ≤ 100 a / g (mL)Ascaris eggs mortality rate, ≥ 95%
Shoot borer, Fruit borer, Stem borer, Hairy caterpillar (on drum stick) and army worm of vegetable crops.
Control measures
1. Andrographis paniculata (siriyanangai) decoction 3 to 5 % or Sida spinosa (Arivalmani Poondu) decoction 5 %
Andrographis paniculata (siriyanangai)
Sida spinosa (Arivalmani Poondu)
Neem Seed
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Neem Seed Kernel
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3. Garlic, Chilli, Ginger extract 500 to 1000 ml per tank (10 litres capacity)
This is a mixture of three plant extracts. 18 grammes of garlic is taken, the outer skin is removed and made into paste. A paste of 9 grammes of green chilli and 9 grammes of ginger is made. All the three pastes are dissolved in 1 litre of water. This mixture is stirred well and filtered before spraying. 500 ml of this extract is made with 100 ml of soap solution and 9.4 litres of water and sprayed on the top.
Vegetable pests: Type-2 (Sucking borers)
Aphids, Green plant hoppers, mealy bugs and white fly
Control measures
1. Andrographis paniculata (siriyanangai) decoction 3 to 5 % or Sida spinosa (Arivalmani Poondu) decoction 5 %
2. Neem Kernel extract 500 to 2000 ml per tank (10 litres capacity)
3. Garlic, Chilli, Ginger extract 500 to 1000 ml per tank (10 litres capacity)
(Preparation mentioned in vegetable pest type-1)
Vegetable pests: Type-3 (Beetles and bugs): Leaf beetle (pumpkin beetle), pod sucking bug, Epilachina beetles of vegetables
Control measures
1. Cow dung extract: Take 1 kg and mix it with 10 litres of water. Filter the extract with a gunny cloth. Add 5 litres of water to the filtrate and again filter it with the same cloth. The filtrate will be a very clear solution. Spray the filtrate on the plants.
2. Andrographis paniculata (siriyanangai) decoction 3 to 5 % or Sida spinosa (Arivalmani Poondu) decoction 5 %
3. Neem Kernel extract 500 to 2000 ml per tank (10 litres capacity)
(Preparation mentioned in vegetable pest type-1)
Vegetable diseases: Tomato wilt, Fusarium wilt in Chilli, Cercospora leaf spot, Yellow mosaic viral disease, alternaria leaf spot and fruit rot of all vegetable crops
Control methods
1. General methods
a. 10 % cow’s urine is sprayed once in 10 days thrice.
b. Half litre cow’s urine along with ½ litre sour butter milk is mixed with 9 litres of water. This is sparyed once in 7 days twice.
C. Cow’s urine and water is mixed in the ratio 1:2. The seeds or roots of seedlings are soaked in this for half an hour before sowing or transplanting .
d. 40 kgs of neem cake per acre is applied as basal manure for vegetable crops to prevent diseases.
e. If there is a disease attack in the nursery, then add 10 % cow’s urine extract along with the water that is used to irrigate the nursery.
2. Fumigation combined with other organic methods
Embelica ribes (Vaividanga)
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Acorus calamus (Vasambu)
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Non chemical other pest control methods
1. Light trap
Light trap
2. Yellow sticky trap
Yellow sticky trap
3. Bird perches: Install ‘T’ shaped bird perches which are long dried twigs @15-20 per acre. These attract birds for resting and the resting birds devour the larvae in the field.
4. Hand picking method: This method of pest is useful if the crop is in a small area. Pour a small amount of kerosene in a polythene bag and pick up the larvae during evening hours and put it in the bag. The pests can be controlled this way without the use of any chemicals. This should be done when the pest numbers are low.
5. Neem as pest repellent:Take neem leaves or Neem cake or Neem kernels and pound it well and place it in a pot. Add twice the volume of water and tie the mouth of the pot with a cloth. Leave it as such for three days. Then, place the pots on all the 4 corners of a field. In the evening, open the mouth of the pots. The foul smell emanating from the neem products prevents entry of pests into the field.
S. No. | Groups | Examples |
N2 fixing Biofertilizers | ||
1. | Free-living | Azotobacter, Beijerinkia, Clostridium, Klebsiella, Anabaena, Nostoc, |
2. | Symbiotic | Rhizobium, Frankia, Anabaena azollae |
3. | Associative Symbiotic | Azospirillum |
P Solubilizing Biofertilizers | ||
1. | Bacteria | Bacillus megaterium var. phosphaticum, Bacillus subtilis Bacillus circulans, Pseudomonas striata |
2. | Fungi | Penicillium sp, Aspergillus awamori |
P Mobilizing Biofertilizers | ||
1. | Arbuscular mycorrhiza | Glomus sp.,Gigaspora sp.,Acaulospora sp., Scutellospora sp. & Sclerocystis sp. |
2. | Ectomycorrhiza | Laccaria sp., Pisolithus sp., Boletus sp., Amanita sp. |
3. | Ericoid mycorrhizae | Pezizella ericae |
4. | Orchid mycorrhiza | Rhizoctonia solani |
Biofertilizers for Micro nutrients | ||
1. | Silicate and Zinc solubilizers | Bacillus sp. |
Plant Growth Promoting Rhizobacteria | ||
1. | Pseudomonas | Pseudomonas fluorescens |
Rhizobium | |
Rhizobium is a soil habitat bacterium, which can able to colonize the legume roots and fixes the atmospheric nitrogen symbiotically. The morphology and physiology of Rhizobium will vary from free-living condition to the bacteroid of nodules. They are the most efficient biofertilizer as per the quantity of nitrogen fixed concerned. They have seven genera and highly specific to form nodule in legumes, referred as cross inoculation group.
Rhizobium inoculant was first made in USA and commercialized by private enterprise in 1930s and the strange situation at that time has been chronicled by Fred (1932).
Initially, due to absence of efficient bradyrhizobial strains in soil, soybean inoculation at that time resulted in bumper crops but incessant inoculation during the last four decades by US farmers has resulted in the build up of a plethora of inefficient strains in soil whose replacement by efficient strains of bradyrhizobia has become an insurmountable problem.
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Azotobacter | |
Of the several species of Azotobacter, A. chroococcum happens to be the dominant inhabitant in arable soils capable of fixing N2 (2-15 mg N2 fixed /g of carbon source) in culture media.
The bacterium produces abundant slime which helps in soil aggregation. The numbers of A. chroococcum in Indian soils rarely exceeds 105/g soil due to lack of organic matter and the presence of antagonistic microorganisms in soil.
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Azospirillum | |
Azospirillum lipoferum and A. brasilense (Spirillum lipoferum in earlier literature) are primary inhabitants of soil, the rhizosphere and intercellular spaces of root cortex of graminaceous plants. They perform the associative symbiotic relation with the graminaceous plants.
The bacteria of Genus Azospirillum are N2 fixing organisms isolated from the root and above ground parts of a variety of crop plants. They are Gram negative, Vibrio or Spirillum having abundant accumulation of polybetahydroxybutyrate (70 %) in cytoplasm.
Five species of Azospirillum have been described to date A. brasilense, A.lipoferum, A.amazonense, A.halopraeferens and A.irakense. The organism proliferates under both anaerobic and aerobic conditions but it is preferentially micro-aerophilic in the presence or absence of combined nitrogen in the medium.
Apart from nitrogen fixation, growth promoting substance production (IAA), disease resistance and drought tolerance are some of the additional benefits due to Azospirillum inoculation.
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Cyanobacteria | |
Both free-living as well as symbiotic cyanobacteria (blue green algae) have been harnessed in rice cultivation in India. A composite culture of BGA having heterocystous Nostoc, Anabaena, Aulosira etc. is given as primary inoculum in trays, polythene lined pots and later mass multiplied in the field for application as soil based flakes to the rice growing field at the rate of 10 kg/ha. The final product is not free from extraneous contaminants and not very often monitored for checking the presence of desiredalgal flora.
Once so much publicized as a biofertilizer for the rice crop, it has not presently attracted the attention of rice growers all over India except pockets in the Southern States, notably Tamil Nadu. The benefits due to algalization could be to the extent of 20-30 kg N/ha under ideal conditions but the labour oriented methodology for the preparation of BGA biofertilizer is in itself a limitation. Quality control measures are not usually followed except perhaps for random checking for the presence of desired species qualitatively.
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Several soil bacteria and fungi, notably species of Pseudomonas, Bacillus, Penicillium, Aspergillusetc. secrete organic acids and lower the pH in their vicinity to bring about dissolution of bound phosphates in soil. Increased yields of wheat and potato were demonstrated due to inoculation of peat based cultures of Bacillus polymyxa and Pseudomonas striata. Currently, phosphate solubilizers are manufactured by agricultural universities and some private enterprises and sold to farmers through governmental agencies. These appear to be no check on either the quality of the inoculants marketed in India or the establishment of the desired organisms in the rhizosphere.
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The transfer of nutrients mainly phosphorus and also zinc and sulphur from the soil milleu to the cells of the root cortex is mediated by intracellular obligate fungal endosymbionts of the genera Glomus, Gigaspora, Acaulospora, Sclerocysts and Endogone which possess vesicles for storage of nutrients and arbuscles for funneling these nutrients into the root system. By far, the commonest genus appears to be Glomus, which has several species distributed in soil.
Availability for pure cultures of AM (Arbuscular Mycorrhiza) fungi is an impediment in large scale production despite the fact that beneficial effects of AM fungal inoculation to plants have been repeatedly shown under experimental conditions in the laboratory especially in conjunction with other nitrogen fixers.
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Silicate solubilizing bacteria (SSB)
Biofertilizers are such as Rhizobium, Azospirillum and Phosphobacteria provide nitrogen and phosphorous nutrients to crop plants through nitrogen fixation and phosphorous solubilization processes. These Biofertilizers could be effectively utilized for rice, pulses, millets, cotton, sugarcane, vegetable and other horticulture crops.
Biofertilizers is one of the prime input in organic farming not only enhances the crop growth and yield but also improves the soil health and sustain soil fertility.
At present, Biofertilizers are supplied to the farmers as carrier based inoculants. As an alternative, liquid formulation technology has been developed in the Department of Agricultural Microbiology, TNAU, Coimbatore which has more advantages than the carrier inoculants.
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- Longer shelf life -12-24 months.
- No contamination.
- No loss of properties due to storage upto 45º c.
- Greater potentials to fight with native population.
- High populations can be maintained more than 109 cells/ml upto 12 months to 24 months.
- Easy identification by typical fermented smell.
- Cost saving on carrier material, pulverization, neutralization, sterilization, packing and transport.
- Quality control protocols are easy and quick.
- Better survival on seeds and soil.
- No need of running Bio-fertilizer production units through out the year.
- Very much easy to use by the farmer.
- Dosages is 10 time less than carrier based powder Bio-fertilizers.
- High commercial revenues.
- High export potential.
- Very high enzymatic activity since contamination is nil.
Host Group | Rhizobium Species | Crops | N fix kg/ha |
Pea group | Rhizobium leguminosarum | Green pea, Lentil | 62- 132 |
Soybean group | R.japonicum | Soybean | 57- 105 |
Lupini Group | R. lupine orinthopus | Lupinus | 70- 90 |
Alfafa grp.Group | R.mellilotiMedicago Trigonella | Melilotus | 100- 150 |
Beans group | R. phaseoli | Phaseoli | 80- 110 |
Clover group | R. trifoli | Trifolium | 130 |
Cowpea group | R. species | Moong, Redgram, Cowpea, Groundnut | 57- 105 |
Cicer group | R. species | Bengal gram | 75- 117 |
- Dull white in colour
- No bad smell
- No foam formation, pH 6.8-7.5
- The colour of the liquid may be blue or dull white.
- Bad odours confirms improper liquid formulation and may be concluded as mere broth.
- Production of yellow gummy colour materials comfirms the quality product.
- Acidic pH always confirms that there is no Azospirillum bacteria in the liquid.
Plant | Mg N2 fixed /g of substrate |
Oryza sativa (Paddy) | 28 |
Sorghum bicolour (Sorghum) | 20 |
Zea mays (Maize) | 20 |
Panicum sp. | 24 |
Cynodon dactylon | 36 |
Setaria sp | 12 |
Amaranthus spinosa | 16 |
- Stimulates growth and imparts green colour which is a characteristic of a healthy plant.
- Aids utilization of potash, phosphorous and other nutrients.
- Encourage plumpness and succulence of fruits and increase protein percentage.
- No growth promotion activity
- Yellowish green colour of leaves, which indicates no fixation of Nitrogen
- A. chroococcum: Produces brown-black pigmentation in liquid inoculum.
- A. beijerinchii: Produces yellow- light brown pigementation in liquid inoculum
- A. vinelandii: Produces green fluorescent pigmentation in liquid inoculum.
- A. paspali: Produces green fluorescent pigmentation in liquid inoculum.
- A. macrocytogenes: Produces, pink pigmentation in liquid inoculum.
- A. insignis: Produces less, gum less, grayish-blue pigmentation in liquid inoculum.
- A. agilies: Produces green-fluorescent pigmentation in liquid inoculum.
- The performance of Azotobacter liquid inoculant was c
- omparatively better than all the treatments in 10 % MS medium followed Azospirillum.
- The performance of Azotobacter liquid inoculant was comparatively better than all the treatments followed by Azosopirillum for the growth of the polybag sugarcane seedlings.
Do
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Don’t
|
Keep Bio-fertilizers bottles away from direct heat and sunlight. Store it in cool and dry place. | Don’t store Bio-fertilizers bottles under heat and sunlight |
Sell only Bio-fertilizers bottles which contain batch number, the name of the crop on which it has to be used, the date of manufacture and expiry period. | Don’t sell Bio-fertilizers bottles after their expiry period is over. |
If the expiry period is over, then discard it as it is not effective. | Don’t prick holes into the bottles or puncture them to pour the content |
Keep Bio-fertilizers bottles away from fertilizer or pesticide containers and they should not be mixed directly. | Do not mix the Bio-fertilizers with fungicides, insecticides, herbicides, herbicides and chemical fertilizers. |
There are three ways of using Liquid Bio-fertilizers
- Seed treatment
- Root dipping
- Soil application
Crop |
Recommended Bio-fertilizer
|
Application method
|
Quantity to be used
|
Field crops Pulses Chickpea, pea, Groundnut, soybean, beans, Lentil, lucern, Berseem, Green gram, Black gram, Cowpea and pigeon pea | Rhizobium | Seed treatment | 200ml/acre |
Cereals Wheat, oat, barley | Azotobacter/Azospirillum | Seed treatment | 200ml/acre |
Rice | Azospirillum | Seed treatment | 200ml/acre |
Oil seeds Mustard, seasum, Linseeds, Sunflower, castor | Azotobacter | Seed treatment | 200ml/acre |
Millets Pearl millets, Finger millets, kodo millet | Azotobacter | Seed treatment | 200ml/acre |
Maize and Sorghum | Azospirillum | Seed treatment | 200ml/acre |
Forage crops and Grasses Bermuda grass, Sudan grass, Napier Grass , ParaGrass, StarGrass etc. | Azotobacter | Seed treatment | 200ml/acre |
Other Misc. Plantation Crops Tobacco | Azotobacter | Seedling treatment | 500ml/acre |
Tea, Coffee | Azotobacter | Soil treatment | 400ml/acre |
Rubber, Coconuts | Azotobacter | Soil treatment | 2-3 ml/plant |
Agro-ForestRY/Fruit Plants All fruit/agro-forestry (herb,shrubs, annuals and perennial) plants for fuel wood fodder, fruits,gum,spice,leaves,flowers,nuts and seeds puppose | Azotobacter | Soil treatment | 2-3 ml/plant at nursery |
Leguminous plants/ trees | Rhizobium | Soil treatment | 1-2 ml/plant |
In biofertilizer production industry, equipments are the major infrastructure, which involves 70 percent of capital investment. Any compromise on the usage of the following mentioned equipments may finally decline in the quality of biofertilizer.After studying the principle behind the usage of all instruments, some of the instruments can be replaced with a culture room fitted with a U.V.Lamp. Autoclaves, Hot Air Oven, Incubators and sealing machines are indigenously made with proper technical specifications. The correct use of equipments will give uninterrupted introduction with quality inoculum.
Essential equipments
Autoclave
It is an apparatus in which materials are sterilized by air free saturated steam (under pressure) at a temperature above 100OC. If the steam pressure inside the autoclave is increased to 15 psi, the temperature will rise to 121°C. this is sufficient to destroy all vegetative cells. Normally all growth medium are sterilized in the autoclave.
|
Laminar air flow chamber
Laminar air flow chamber provides a uniform flow of filtered air. This continuous flow of air will prevent settling of particles in the work area.Air borne contamination is avoided in this chamber. Culture transfers and inoculation can be done here.
|
BOD incubators
Incubators providing controlled conditions (light, temperature, humidity, etc.) required for the growth and development of microorganisms. Multiplication of starter culture can be done in this instrument.
|
A fermentor is the equipment, which provides the proper environment for the growth of a desired organism.
It is generally a large vessel in which, the organism may be kept at the required temperature, pH , dissolved oxygen concentration and substrate concentration. Different models of fermentors are available depending upon the necessity.
A simple version model contains steam generator, sterilization process devices and agitator.
A sophisticated fermentor contains pH regulator, oxygen level regulator, anti-foam device, temperature controller, etc.
|
Azospirillum | Rhizobium | Phosphobacteria | Azotobacter |
- The mass production of carrier based bacterial biofertilizers involves three stages.
- Culturing of microorganisms
- Processing of carrier material
- Mixing the carrier and the broth culture and packing
The media used for mass culturing are as follows:
Mannitol | - | 10.0 g |
K2 HPO4 | - | 0.5 g |
Mg So4 7H2 O | - | 0.2 g |
NaCl | - | 0.1 g |
Yeast extract | - | 0.5 g |
Agar | 20.0 g | |
Distilled water | 1000.0 ml |
Malic acid | - | 5.0g |
Potassium hydroxide | - | 4.0g |
Dipotassium hydrogen orthophosphate | - | 0.5g |
Magnesium sulphate | - | 0.2g |
Sodium chloride | - | 0.1g |
Calcium chloride | - | 0.2g |
Fe-EDTA (1.64% w/v aqueous) | - | 4.0 ml |
Trace element solution | - | 2.0 ml |
BTB (0.5% alcoholic solution) | - | 2.0 ml |
Agar | - | 1.75 g |
Distilled water | - | 1000 ml |
pH | - | 6.8 |
Trace element solution | ||
Sodium molybdate | - | 200 mg |
Manganous sulphate | - | 235 mg |
Boric acid | - | 280 mg |
Copper sulphate | - | 8 mg |
Zinc sulphate | - | 24 mg |
Distilled water | - | 200 ml |
Mannitol | : | 10.0 g |
Ca CO3 | : | 5.0 g |
K2HPO4 | : | 0.5 g |
Mg SO4.7H2O | : | 0.2 g |
NaCl | : | 0.2 g |
Ferric chloride | : | Trace |
MnSO4.4H2O | : | Trace |
N-free washed Agar | : | 15.0 g |
pH | : | 7.0 |
Distilled Water | : | 1000 ml |
Glucose | : | 10.0 g |
Ca3(PO4)2 | : | 5.0 g |
(NH4)2SO4 | : | 0.5 g |
KCl | : | 0.2 g |
MgSO4. 7H2O | : | 0.1 g |
MnSO4 | : | Trace |
FeSO4 | : | Trace |
Yeast Extract | : | 0.5 g |
Distilled Water | : | 1000 ml |
- Prepare appropriate media for specific to the bacterial inoculant in 250 ml, 500 ml, 3 litre and 5 litre conical flasks and sterilize.
- The media in 250 ml flask is inoculated with efficient bacterial strain under aseptic condition
- Keep the flask under room temperature in rotary shaker (200 rpm) for 5- 7 days.
- Observe the flask for growth of the culture and estimate the population, which serves as the starter culture.
- Using the starter culture (at log phase) inoculate the larger flasks (500 ml, 3 litre and 5 litre) containing the media, after obtaining growth in each flask.
- The above media is prepared in large quantities in fermentor, sterilized well, cooled and kept it ready.
- The media in the fermentor is inoculated with the log phase culture grown in 5 litre flask. Usually 1 -2 % inoculum is sufficient, however inoculation is done up to 5% depending on the growth of the culture in the larger flasks.
- The cells are grown in fermentor by providing aeration (passing sterile air through compressor and sterilizing agents like glass wool, cotton wool, acid etc.) and given continuous stirring.
- The broth is checked for the population of inoculated organism and contamination if any at the growth period.
- The cells are harvested with the population load of 109 cells ml-1 after incubation period.
- There should not be any fungal or any other bacterial contamination at 10-6 dilution level
- It is not advisable to store the broth after fermentation for periods longer than 24 hours. Even at 4o C number of viable cells begins to decrease.
- Cheaper in cost
- Should be locally available
- High organic matter content
- No toxic chemicals
- Water holding capacity of more than 50%
- Easy to process, friability and vulnerability.
|
- The neutralized, sterilized carrier material is spread in a clean, dry, sterile metallic or plastic tray.
- The bacterial culture drawn from the fermentor is added to the sterilized carrier and mixed well by manual (by wearing sterile gloves) or by mechanical mixer. The culture suspension is to be added to a level of 40 – 50% water holding capacity depending upon the population.
- The inoculant packet of 200 g quantities in polythene bags, sealed with electric sealer and allowed for curing for 2 -3 days at room temperature ( curing can be done by spreading the inoculant on a clean floor/polythene sheet/ by keeping in open shallow tubs/ trays with polythene covering for 2 -3 days at room temperature before packaging).
- The polythene bags should be of low density grade.
- The thickness of the bag should be around 50 – 75 micron.
- Each packet should be marked with the name of the manufacturer, name of the product, strain number, the crop to which recommended, method of inoculation, date of manufacture, batch number, date of expiry, price, full address of the manufacturer and storage instructions etc.,
- The packet should be stored in a cool place away from the heat or direct sunlight.
- The packets may be stored at room temperature or in cold storage conditions in lots in plastic crates or polythene / gunny bags.
- The population of inoculant in the carrier inoculant packet may be determined at 15 days interval. There should be more than 109 cells / g of inoculant at the time of preparation and107 cells/ g on dry weight basis before expiry date.
1. Tank for mass multiplication of AM | 2. Sprinkling of water in tank with vermiculite | 3. Making of furrows to sow maize seeds |
4. Sowing the seeds in furrows | 5. View of the maize sown AM pit | 6. Vermiculite contained raised AM infected maize plants |
- A trench (1m x 1m x 0.3m) is formed and lined with black polythene sheet to be used as a plant growth tub.
- Mixed 50 kg of vermiculite and 5 kg of sterilized soil and packed in the trench up to a height of 20 cm
- Spread 1 kg of AM inoculum (mother culture) 2-5 cm below the surface of vermiculite
- Maize seeds surface sterilized with 5% sodium hypochlorite for 2 minutes are sown
- Applied 2 g urea, 2 g super phosphate and 1 g muriate of potash for each trench at the time of sowing seeds. Further 10 g of urea is applied twice on 30 and 45 days after sowing for each trench
- Quality test on AM colonization in root samples is carried out on 30th and 45th day
- Stock plants are grown for 60 days (8 weeks). The inoculum is obtained by cutting all the roots of stock plants. The inoculum produced consists of a mixture of vermiculite, spores, pieces of hyphae and infected root pieces.
- Thus within 60 days 55 kg of AM inoculum could be produced from 1 sq meter area. This inoculum will be sufficient to treat 550 m2 nursery area having 11,000 seedlings.
For existing trees: Two hundred gram of VAM inoculum is required for inoculating one tree. Apply inoculum near the root surface at the time of fertilizer application.
Blue green algal inoculation with composite cultures was found to be more effective than single culture inoculation. A technology for mass scale production of composite culture of blue green algae under rice field condition was developed at TNAU and the soil based BGA inoculum could survive for more than 2 years.
At many sites where algal inoculation was used for three to four consecutive cropping seasons, the inoculated algae establish well and the effect persisted over subsequent rice crop. Technologies for utilizing nitrogen fixing organisms in low land rice were the beneficial role of blue green algal inoculation in rice soils of Tamil Nadu.
The blue green algal inoculum may be produced by several methods viz., in tubs, galvanized trays, small pits and also in field conditions. However the large-scale production is advisable under field condition which is easily adopted by farmers.
|
- Big metallic trays (6’x 3’x 6”lbh) can be used for small scale production
- Take 10 kg of paddy field soil, dry powder well and spread
- Fill water to a height of 3”
- Add 250 g of dried algal flakes (soil based) as inoculum
- Add 150 g of super phosphate and 30 g of lime and mix well with the soil
- Sprinkle 25 g carbofuran to control the insects
- Maintain water level in trays
- After 10 to 15 days, the blooms of BGA will start floating on the water sources
- At this stage stop watering and drain. Let the soil to dry completely
- Collect the dry soil based inoculum as flakes
- Store in a dry place. By this method 5 to 7 kg of soil based inoculum can be obtained.
- Rice field
- Super phosphate
- Carbofuran
- Composite BGA starter culture
Select an area of 40 m2 (20m x 2m) near a water source which is directly exposed to sunlight.
Make a bund all around the plot to a height of 15 cm and give it a coating with mud to prevent loss of water due to percolation.
- Plot is well prepared and levelled uniformly and water is allowed to a depth of 5-7.5 cm and left to settle for 12 hrs.
- Apply 2 kg of super phosphate and 200 g lime to each plot uniformly over the area.
- The soil based composite starter culture of BGA containing 8-10 species @ 5 kg / plot is powdered well and broadcasted.
- Carbofuran @ 200 g is also applied to control soil insects occurring in BGA.
- Water is let in at periodic intervals so that the height of water level is always maintained at 5 cm.
- After 15 days of inoculation, the plots are allowed to dry up in the sun and the algal flakes are collected and stored.
The floating algal flasks are green or blue green in colour. From each harvest, 30 to 40 kg of dry algal flakes are obtained from the plot.
Method of inoculation of BGA in rice field
Blue green algae may be applied as soil based inoculum to the rice field following the method described below.
- Powder the soil based algal flakes very well.
- Mix it with 10 kg soil or sand (10kg powdered algal flakes with 10 kg soil / sand).
- BGA is to be inoculated on 7-10 days after rice transplanting.
- Water level at 3-4” is to be maintained at the time of BGA inoculation and then for a month so as to have maximum BGA development.
A week after BGA inoculation, algal growth can be seen and algal mat will float on the water after 2-3 weeks. The algal mat colour will be green or brown or yellowish green.
- One cent (40 sq.m) area plot
- Cattle dung
- Super phosphate
- Furadan
- Fresh Azolla inoculum
- Select a wetland field and prepare thoroughly and level uniformly.
- Mark the field into one cent plots (20 x 2m) by providing suitable bunds and irrigation channels.
- Maintain water level to a height of 10 cm.
- Mix 10 kg of cattle dung in 20 litres of water and sprinkle in the field.
- Apply 100 g super phosphate as basal dose.
- Inoculate fresh Azolla biomass @ 8 kg to each pot.
- Apply super phosphate @ 100 g as top dressing fertilizer on 4th and 8th day after Azolla inoculation.
- Apply carbofuran (furadan) granules @ 100 g/plot on 7th day after Azolla inoculation.
- Maintain the water level at 10 cm height throughout the growth period of two or three weeks.
- Observations
- Note the Azolla mat floating on the plot. Harvest the Azolla, drain the water and record the biomass.
- Collect the fresh Azolla biomass from the Azolla nursery plot.
- Prepare the wetland well and maintain water just enough for easy incorporation.
- Apply fresh Azolla biomass (15 t ha-1) to the main field and incorporate the Azolla by using implements or tractor.
- Select a transplanted rice field.
- Collect fresh Azolla inoculum from Azolla nursery.
- Broadcast the fresh Azolla in the transplanted rice field on 7th day after planting (500 kg / ha).
- Maintain water level at 5-7.5cm.
- Note the growth of Azolla mat four weeks after transplanting and incorporate the Azolla biomass by using implements or tranctor or during inter-cultivation practices.
- A second bloom of Azolla will develop 8 weeks after transplanting which may be incorporated again.
- By the two incorporations, 20-25 tonnes of Azolla can be incorporated in one hectare rice field.
2. Seedling root dip
3. Main field application
Combined application of bacterial biofertilizers.
- Bacterial inoculants should not be mixed with insecticide, fungicide, herbicide and fertilizers.
- Seed treatment with bacterial inoculant is to be done at last when seeds are treated with fungicides.
Crop | Seed | Nursery | Seedling dip | Main field | Total requirement of packets per ha |
Rice | 5 | 10 | 5 | 10 | 30 |
Sorghum | 3 | - | - | 10 | 13 |
Pearl millet | 3 | - | - | 10 | 13 |
Ragi | 3 | - | 5 | 10 | 18 |
Maize | 3 | - | - | 10 | 13 |
Cotton | 3 | - | - | 10 | 13 |
Sunflower | 3 | - | - | 10 | 13 |
Castor | 3 | - | - | 10 | 13 |
Sugarcane | 10 | - | - | 36 (3 split) | 46 |
Turmeric | - | - | - | 24 (2 split) | 24 |
Tobacco | 1 | 3 | - | 10 g/pit | 14 |
Papaya | 2 | - | - | 10 | - |
Mandarin Orange | 2 | - | - | 10 g/pit | - |
Tomato | 1 | - | - | 10 | 14 |
Banana | - | - | 5 | 10 g/pit | - |
Crop | Total requirement of packets per ha |
Soybean | 5 |
Groundnut | 5 |
Bengalgram | 5 |
Blackgram | 3 |
Greengram | 3 |
Redgram | 3 |
Cowpea | 3 |
The recommended dosage of Azospirillum is adopted for phosphobacteria inoculation; for combined inoculation, both biofertilizers as per recommendations are to be mixed uniformly before using.
Animal | Dosage / day |
Adult cow , Buffalo, Bullock | 1.5-2 kg |
Layer, Broiler birds | 20 – 30 grams |
Goat | 300 – 500 grams |
Pig | 1.5 – 2.0 kg |
Rabbit | 100 gram |
The Azolla feeding to layer birds increase egg weight, albumin, globulin and carotene contents. The total protein content of the eggs laid by the Azolla fed birds is high and the total carotene content of Azolla eggs(440 g 100 g-1 of edible portion)is also higher than the control. The rapid biomass production due to the high relative growth rate, increased protein and carotene contents and good digestability of the Azolla hybrid Rong ping favour its use as an effective feed supplement to poultry birds.
Parameters | Azolla egg | Control | percentage increase over control |
Egg weight (g) | 61.20 | 57.40 | 6.62 |
Albumin (g /100 g of edible portion) | 3.9 | 3.4 | 14.70 |
Globulin (g /100 g of edible portion) | 10.1 | 9.5 | 6.31 |
Total protein (g/ 100 g of edible portion) | 14.0 | 12.9 | 8.52 |
Carotenes (µg / 100 g of edible portion) | 440 | 405 | 8.64 |
Azolla mass multiplication in pits | Feeding Azolla to Rabbit |
Feeding Azolla to Poultry | Feeding Azolla to Livestock |
Inoculating Super phosphate and Cow dung in Azolla pit |
Department of Agricultural Microbiology, Agriculture College and Research Institute, Tamil Nadu Agricultural University Dr. S. Anthoniraj MADURAI-625 104 ( 0452-422956 fax: 422785 e-mail: s_anthoniraj@yahoo.com | Biofertilizer Production Unit, Department of Agriculture, Govt. of Tamil Nadu Gundusalai Road, Sommandalam, CUDDALORE-607 001 (TN) |
Biofertilizer Production Unit, Department of Agriculture, Govt. of Tamil Nadu Agricultural Chemist Sakkottai, THANTAVUR-612 401 (TN) | Biofertilizer Production Unit, Department of Agriculture, Govt. of Tamil Nadu Jamal Mohd. College Post, Khajamalai, TRICHY-620 020 (TN) |
KRIBHCO Sidco Garment Complex, Thiruvika Industrial Estate, Guidy, CHENNAI-32 | Regional Research Station Tamil Nadu Agricultural University, PIYUR-635 112 Via-Kaveripattinam Dharmapuri District ( 04343-50043 |
Monarch Bio-Fertilisers and Research Centre 12, SIDCO Industrial Estate, Thirumazhisai, CHENNAI-602 107 (TN) ( 6272780 | Lakshmi Bio-Tech Mr. V. Sithanandham Nellikuppam Road, Thottapattu, CUDDALORE-607 109 (TN) ( 04142-210136 |
Marygreen Afrotech (P) Ltd. Dr. Y. Joe 5/302, Srisaibaba St., Santosh Nagar, Kandanchavadi, Perungudi Post, CHENNAI-600 096 (TN) 4964202, 4745957 e-mail: marygreen45@hotmail.com | Tamil Nadu Agricultural University Prof. & Head Deptt. of Agricultural Microbiology, COIMBATORE-3 (TN) ( 431222 ext. 294 Fax: 0422-431672 e-mail: vctnau@vsnl.com |
T Stanes & Company Limited Dr. S. Ramarethinam 8/23-24, Race Course Road, COIMBATORE-641 018 (TN) ( 0422-211514, 213515 Fax: 217432 e-mail: tstanes@vsnl.com | Esvin Advanced Technologies Limited Mr. T. S. Venkataraman “Esvin House” Perungudi, CHENNAI-600 096 (TN) ( 4961056,4960690 Fax: 4961002 e-mail: tsv@vsnl.com |
Southern Petrochemical Industries Corporation Limited, Mr. K. Raju SPIC Ltd. Biotechnology Division, Chettiar Agaram Road, Gandhi Nagar, Porur, CHENNAI-600 116 (TN) ( 044-4768064 Tele-Fax: 044-4767347 e-mail: biotech.por@spic.co.in | Biofertiliser Unit-Manali, Madras Fertilizers Limited Mr. P. Mallikarjuna Reddy Chief Manager –Bioproducts Commercial Group, Madras Fertilizers Ltd., Manali, CHENNAI-600 068 (TN) ( 044-5941001 ext. 2750 Fax: 5941010 e-mail: edcomm@mfl.tn.nic.in |
Biofertilizer Production Unit Mr. S. Murugan Agricultural Chemist, Biofertilizer Production Unit, Seelanaickenpatty, SALEM-636 201 (TN) | Biofertilizer Production Unit, Mr.Thiru P. Raman Agricultural Chemist, Biofertilizer Production Unit, KUDUMIAMALAI-622 104 Distt. Pudukkottai |
Main Biocontrol Research Laboratory (Unit of Tamilnadu Cooperative Sugar Federation) 2E/1, Rajeshwari Vedhachalam Street, CHENGALPATTU-603 001 (TN) ( 04114-431393 | The SIMA Cotton Development and Research Association Dr. M.A. Shanmugham “Shanmukha Manram”, Post Box No. 3871, Race Course, COIMBATORE-641 018 (TN) ( 0422-211391 Tele-Fax: 0422-216798 |
- Use of improper, less efficient strains for production.
- Lack of qualified technical personnel in production units.
- Unavailability of good quality carrier material or use of different carrier materials by different producers without knowing the quality of the materials.
- Production of poor quality inoculants without understanding the basic microbiological techniques
- Short shelf life of inoculants.
- Non-availability of suitable facilities for production
- Lack of essential equipments, power supply, etc.
- Space availability for laboratory, production, storage, etc.
- Lack of facility for cold storage of inoculant packets
- Non-availability of sufficient funds and problems in getting bank loans
- Less return by sale of products in smaller production units.
- Seasonal demand for biofertilizers
- Simultaneous cropping operations and short span of sowing/planting in a particular locality
- Soil characteristics like salinity, acidity, drought, water logging, etc.
- Lack of technically qualified staff in the production units.
- Lack of suitable training on the production techniques.
- Ignorance on the quality of the product by the manufacturer
- Non-availability of quality specifications and quick quality control methods
- No regulation or act on the quality of the products
- Awareness on the technology
- Unawareness on the benefits of the technology
- Problem in the adoption of the technology by the farmers due to different methods of inoculation.
- No visual difference in the crop growth immediately as that of inorganic fertilizers.
- Unawareness on the benefits of the technology.
- Problem in the adoption of the technology by the farmers due to different methods of inoculation.
- No visual difference in the crop growth immediately as that of inorganic fertilizers.
- Unawareness on the damages caused on the ecosystem by continuous application of inorganic fertilizer.
- Non availability of right inoculant at the right place in right time.
- Lack of retain outlets or the market network for the producers.
Azospirillum | Strains |
Normal soils | Az. 204 |
Acid soils | Az Y2 |
Dry lands | Azt. 11 |
Paddy | Az 204 (Azospiriluml lipoferum) |
Other Crops | Az Sp 7 (Azospirilum brasilense) |
Azotobacter | |
All Crops | Az1 (Azotobacter chroococcum) |
Gluconacetobacter | |
Sugarcane | Pal 5 (Gluconacetobacter diazotropicus) |
Rhizobium | |
Groundnut | TNAU 14 |
Soybean | Cos 1 |
Cowpea | Coc 10 |
Redgram | Cc 1, CPR 9 |
Greengram &Blackgram | COG 15, BMBS 47 |
GMBS 1 | |
Greengram | COG15 |
Bengalgram | CoBe 13 |
Tree Legumes | ALM 16 |
Phosphobacteria | |
All crops | PB 1, PS 1 (Bacillus megaterium) |
Potash Bacteria | KRB 9 (Bacillus muscilagenosus) |
S. No. | Particulars | Amount (Rs.in lakhs) |
I. | Expenditure* | |
A. | Capital Investment (Fixed cost) | |
i. | Building including cost of site (App. 1200 sq. ft.) | 12.00 |
ii. | Equipment and apparatus | 41.00 |
B. | Operational cost (variable cost) | |
i. | Working capital (Raw materials) | 10.00 |
ii. | Staff salary | 2.04 |
iii. | Labour | 2.50 |
iv. | Electricity | 0.50 |
v. | Travelling expenses | 0.50 |
vi. | Administrative expenses | 0.50 |
vii. | Interest on loan and depreciation | 0.70 |
viii. | Miscellaneous expenses | 0.26 |
Total (variable cost) | 17.00 | |
Total investment | 70.00 | |
Actual initial investment | 50.00 |
S.No. | Equipment and apparatus | Qty (Nos.) | Amount (Rs.in lakhs) |
1. | Fermentor (200 lit. capacity) | 4 | 26.00 |
2. | Shaker | 2 | 1.50 |
3. | Laminar air flow chamber | 1 | 0.60 |
4. | Autoclave | 2 | 0.30 |
5. | Hot air oven | 1 | 0.10 |
6. | Incubator | 1 | 0.10 |
7. | Refrigerator | 1 | 0.30 |
8. | Microscope | 1 | 0.75 |
9. | pH meter | 1 | 0.15 |
10. | Physical balance | 1 | 0.10 |
11. | Electronic balance | 1 | 0.75 |
12. | Counter-poise balance | 5 | 0.25 |
13. | Sealing machine | 5 | 0.25 |
14. | Work benches | 4 | 0.30 |
15. | Plastic trays | 50 | 0.25 |
16. | Trays (Zinc/Aluminium) | 10 | 0.20 |
17. | Trolley | 1 | 0.10 |
18. | Automatic packing machine (optional) | 1 | 9.00 |
Total | 41.00 |
cost of mother culture |
:
| 0.05 |
Glasswares |
:
| 0.70 |
Chemicals |
:
| 2.50 |
Polythene bags |
:
| 3.50 |
Carrier materials |
:
| 3.00 |
Miscellaneous items |
:
| 0.25 |
Total |
:
|
10.00
|
Technical staff (1 No.) | : | 9000 x 12 | 1,08,000 |
Laboratory staff (2 Nos.) | : | 4000 x 2 x 12 | 96,000 |
Total
|
2,04,000
|
60% capacity | : | 90 MT per year |
75% capacity | : |
112.5 MT per year
|
100% capacity
| : | 150 MT per year |
Cost of 1 kg of biofertilizer (present Govt./University rate) |
:
| Rs.25/- |
Cost of 90 MT (60% capacity) |
:
|
22.500 lakh rupees
|
112.5 MT (75% capacity) |
:
| 28.125 lakh rupees |
135 MT (90% capacity) |
:
| 33.750 lakh rupees |
150 MT (100% capacity) |
37.500 lakh rupees
|
Year | Production | Receipt (Lakh Rs.) | Expenditure (Lakh Rs.) | Gain (Lakh Rs.) |
I | 60% | 22.500 | 50.000 | -27.500 |
II | 75% | 28.125 | 18.700* | 9.425 |
III | 90% | 33.750 | 20.570* | 13.180 |
IV | 100% | 37.500 | 22.630* | 14.870 |
Profit anticipated after 4 years | 9.975 |
Capital cost ( for construction of pits size of 4x 3x1.5 ft including construction material sand labour cost) | Rs.3,000/- |
Inoculum cost ( from TNAU) 20 KG @ Rs.20/- per kg | Rs.400/- |
Vermiculite cost (including transport charges) 500kg@ Rs.6.50 | Rs.3,250/- |
Labour cost-Since it is a single pit, family members can look after | NA |
Seed materials and mesh for covering for pits | Rs.100+100 |
Quality control charges at TNAU (This will be done after 1 year and before selling the product & need not be carried out after each harvest) | Rs.1,000/- |
Bag- cost of packing the materials-30 @ Rs.10 each Labour cost of harvesting and packing | Rs.300/- Rs.200/- |
Total | Rs.8,350/- |
Benefit expected by the sale of produced inoculum 500kg @ Rs.20/- per kg (In TNAU) Rs.35/- per kg ( In Private) | Rs.10,000/- Rs.17,500/- |
Net Income ( First harvest) Rs.10,000-8,350( Sl.No.8 – Sl.No 1 to 7) Rs.17,500-8,350 | Rs.1,197/- Rs.9,150/- |
For the II harvest the cost will be | Rs.4,950/- |
From the second harvest benefit will be of Rs.10,000/ - Rs.4,950/ Rs.17,500/ - Rs.4,950/ | Rs. 5,050/- Rs.12,550/- |
The Net Income for one year will be Rs.50,000/ -Rs.24,750/ Rs.87,500/ -Rs.24,750/ | Rs.25,250/- Rs.62,750/- |
Name of Biofertilizers | Cost of Biofertilizers | Availabilty |
Azospirillum | Rs.40/Kg | Professor and Head Department of Agricultural Microbiology Tamil Nadu Agricultural University Coimbatore - 641 003 Phone: 91-422-6611294 Fax: 91-422-2431672 Email: microbiology@tnau.ac.in |
Liquid Biofertilizer | Rs.300/lit | |
Phosphobacteria | Rs.40/Kg | |
Rhizobium | Rs.40/Kg | |
Azotobacter | Rs.40/Kg | |
VAM | Rs.30/Kg | |
Azolla | Rs.5/Kg |