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Quality Control

RBDC, Imphal has a lab for testing the quality of the products. As a voluntary service to the farmers and channelising agencies, RBDC undertakes the quality analysis of all types of biofertilizers. This service is free for all. As the quality parameters are highly technical, it is not to be done at farmers end. Details of Quality control analysis since inception at RBDC is as follows :

Year Sample Tested Sub-Standard
1995-96 84 6
1996-97 67 -
1997-98 49 -
1998-99 55 -
1999-00 42 -
2000-01 26 -
2001-02 30 4
2002-03 69 16

How to send the sample 

The sample should be sent in the forms of packet/parcel for each batch to be tested (preferably in two packets) for quality analysis. The address of the sender should be mentioned clearly in case the result is to be delivered by post. The result/report will be provided within 15-30 days time.

Precaution

As bioferlilizers are live product, they should be handled carefully and shall not be exposed to heat and direct sunlight. While sending for testing, the packet/parcel should be properly sealed and intact.

Standard values of biofertilizes

Parameters Rhizobium Azotobacter Azospirillium

PSM

Total Viable count within 15 days of manufacture >1X108 > 1X107 >1X108 >1X108
Contamination Nil Nil Nil Nil
Total Viable count within 15 days before Expiry > 1X107 > 1X106 > 1X107 > 1X107
PH Value 6.0-7.5 6.0-7.5 6.0-7.5 6.0-7.5
Strain Efficiency Capable of producing good modulation. dry weight of treated plants should be 50% more over control Capable of fixing 10mg of N/gm of sucrose consumed Capable of fixing 10mg of N/gm of malate used Capable of developing a P-solubilization zone of > 10mm

Testing quality of biofertilizers at user’s end

To obtain good results, the biofertilizer packet must contain all the traits in general and appropriate microbial load of appropriate strain in particular as mentioned earlier, but as the quality requirements are very specific and require the services of a full fledged quality control laboratory, it is very difficult to ascertain it as user’s point. However, for personal satisfaction one can use following method to evaluate the efficacy of the product. But remember this is only a qualitatively indicator method and its correctness varies widely depending upon handling and materials.

Steps to follow :

1 Take 4-5 kgs of good garden soil and sterilize it in a pressure cooker for 30-40 minutes. After cooling fill this soil in 6 small pots.
2 Select the right combination of seed and biofertilizer.
3 Treat half of the seeds with appropriate biofertilizer using standard seed treatment method.
4 3 pots should be sown with treated seeds while 3 pots be sown with untreated seeds to serve as control.
5 Keep the pots in protected open space and ensure daily watering.
6 Observe after 30-40 days.

Observation :

RHIZOBIUM In case of leguminous seeds treated with right type of Rhizobium biofertilizer, the treated plants will show adequate nodulation on roots with higher plant weight compared to untreated control, which will show either no or very few small nodules.
AZOTOBACTER/
AZOSPIRILLUM
In case of non legume, treat appropriate test host seeds (such as maize) with Azotobacter or Azospirillium biofertilizer, the treated plant will be healthier, having green colour and higher plant weight compared to untreated control which will show lesser plant weight and pale green plant colour.

Criteria for geting good response of biofertilizers

1 Product must contain good effective strain in appropriate population should be free from   contaminating microorganisams.
2 Select right combination of biofertilizers and use before expiry.
3 Use appropriate method of application and apply at appropriate time.
4 For seed treatment use adequate adhesive for better results.
5 For problematic soils use corrective methods like lime or gypsum pelleting of seeds or correction of soil pH by use of lime.
6 Ensure the supply of phosphorus and other nutrients.

Reasons for poor response

1

On accounts of quality of product.
  a) Use of ineffective strain.
  b) Insufficient population of microorganisams
  c) High level of contaminants

2

On account of inadequate storage facilities
  a) May have been exposed to high temperature
  b) May have been stored in hostile conditions.

3

On account of usage
  a) Not used by recommended method in appropriate doses
  b) Poor quality adhesive
  c) Used with strong doses of plant protection chemicals

4

On account of soil and environment
  a) High soil temperature or low soil moisture
  b) Acidity or alkalinity in soil
  c) Poor availability of phosphorous and molybdenum
  d) Presence of high native population or presence of bacteriophages

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