SEED TESTING METHODS,

PROCEDURES AND
LABORATORY STANDARDS
National Seed Quality Control Services

Keven Mark Jimenez

Seed A nalyst
NATIONAL SEED QUALITY CONTROL SERVICES
SEED TESTING
 first seed quality control scheme developed to determine the
planting value of seeds

 developed to avoid hazards in crop production due to planting of

inferior seeds

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 Seed Testing
Procedures for seed testing
in accordance with the rules
and regulations of the
International Seed Testing
Association (ISTA) or what is
sanctioned by the National
Seed Industry Council thru
Technical Working Group on
Seed Certification and
Standards
Reasons for Testing Seeds
1. To determine quality or suitability of seed for sowing purposes.
2. To obtain information for labeling seeds, especially seed stocks.
3. To obtain information for basis of distribution, storage and
disposition of seeds.
4. To obtain information for basis of buying and selling.

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Other Reasons
1. For the evaluation of research in seed technology.
2. To determine the processing and blending procedures and to
evaluate the blending process.
3. To determine the potential and actual seed quality problems and
to offer solutions to these problems.

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 Routing a Sample Through the Seed Testing Laboratory

Submitted sample Moisture content File bulk seed

determination sample,purity, other
varieties fraction
Registration, receiving, Purity Test
weighing of submitted sample
Check Result

Germination Test
Mixing, dividing, obtaining and
weighing of working sample Report results

Evaluating Germination
test Issue appropriate results,
tags, seals
Determination of other
varieties
To Seed inspector, seed
Other test producer
 Routing a Sample Through the Seed Testing Laboratory

Submitted sample Moisture content File bulk seed

determination sample,purity, other
varieties fraction
Registration, receiving, Purity Test
weighing of submitted sample
Check Result

Germination Test
Mixing, dividing,obtaining and
weighing of working sample Report results

Evaluating Germination
test Issue appropriate results,
tags, seals
Determination of other
varieties
To Seed inspector, seed
Other test producer
MOISTURE CONTENT
DETERMINATION

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 IMPORTANCE OF MOISTURE
TESTING
Moisture content

 used as an index for the proper time of harvesting.

 affects the mechanical efficiency and the degree of

mechanical seed damage incurred during harvesting and
processing of grain crops.

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Moisture Content (MC)
 Very critical determinant of seed longevity and grain
quality during storage.

 1% difference in moisture content can increase or

decrease seed longevity two times.

 ISTA Rules are used to determine the MC of the seeds.

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Moisture Content (MC)
Milling recovery in rice is affected by grain MC

Accurate determination of grain moisture is economically important

For valid interpretation of results in the evaluation of varietal

performance in seed yield and in seed storage (crop research) =
accurate MC determination is a MUST!

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 METHODS OF MOISTURE
CONTENT DETERMINATION

1. Secondary or Practical Method

2. Primary or Oven Method

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Secondary or Practical
Method
MC is taken by moisture meters wherein a direct reading
scale or print out is obtained.

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 Secondary or Practical
Method
Kett digital and
Kett riceter

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Primary or Oven Method
Moisture content is calculated directly from the weight loss
due to removal of moisture.

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Oven Method

Determination of
Moisture Content
Using Oven Method

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Oven Method
Objective
 To determine the moisture content of seed by methods suitable
for routine use.
Definition
 The moisture content of a sample is the loss in weight when it is
dried.
 Expressed as a percentage of the weight of the original sample.

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Oven Method
Principle
 The methods prescribed are designed to reduce
oxidation, decomposition or the loss of other volatile
substances while ensuring the removal of as much
moisture as possible.

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 Apparatus

Adjustable Constant-Temperature Oven

Grinding Mill
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3. Accessories for oven method

Desiccator Containers Tong

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Analytical Balance

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Procedure
1. Submitted sample is accepted for moisture determination
(only if it is in an intact, moisture – proof container from
which as much air as possible has been excluded).
2. Determination shall be started as soon as possible after
receipt.

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Prescribed Methods
1.Low Constant Temperature Oven Method

2.High Constant Temperature Oven Method

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 Low Constant Temperature Oven
Method
103 + 2 °C dry for 17 + 1 hours

1.Working sample must be evenly distributed over the

surface of the container.
2.Weigh the container and its cover before and after filling.

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 Low Constant Temperature Oven
Method
3.Place the container rapidly on top of its cover, in an oven
maintained at 103 + 2 °C dry for 17 + 1 hours.
4.The drying period begins at the time the oven returns to
the required temperature.
5.At the end of the prescribed period cover the container
and place in a desiccator to cool for 30 – 45 mins.

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 Low Constant Temperature Oven
Method
6.After cooling, weigh the container with its cover and
contents.
7.The relative humidity of the ambient air in the laboratory
must be less than 70% when the determination is carried
out.

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 High Constant Temperature Oven
Method
 Procedure same as in LCT oven method
 Temperature range is 130 – 133°C
 Corn dried for 4 hours
Other cereals (rice, sorghum) – 2 hours
Other species – 1 hour

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 Computation of MC Using Oven
Method
MC = W1 – W2 x 100
W1
MC = _____%
Where:
W1 = weight of seed before drying
W2 = weight of seed after drying
MC = Moisture Content

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Tolerance
The difference between 2 replications should be 0.2%.
However, if the results of the two replications are more
than this value, re – testing should be done.

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Species for Which Low Constant Temperature
(103oC) Oven Method is Used

Onion Radish All tree sp.

Peanut Eggplant
Mustard Pepper
Pechay Soybean
Cabbage Cotton
Cauliflower

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 Species for Which High Constant Temperature
(130oC) Oven Method is Used
CeleryTomato Patola
Asparagus Rice Squash
Beets Beans Kangkong
WatermelonPeas Upo
Cucumber Sorghum Ampalaya
Melon Spinach Tobacco
CarrotWheat Lettuce
Corn

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Illustrated Procedure for
Moisture Content
Determination

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 Weighing of Tin Cans

Grinding of Seeds

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 Oven Method

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Tin Cans in the Dessicator

Weighing of Dried Seeds

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 Working Sheet for MC

Recording Sheet for MC

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SEED STANDARDS

Factors Breeder Foundation Registered Certified

Seed Seed Seed Seed

Moisture content (max.) 14% 14% 14% 14%

Problem solving:

Given: Fresh Weight- 5,000 kg

Field MC- 20%

Find: Weight of palay Seed at 14% MC

Formula: 100-Field MC x Fresh Weight

100-14

Solution:
= 100-20 x 5,000
100-14

= 80 x 5,000 =4,651 kg
86
 Routing a Sample Through the Seed Testing Laboratory

Submitted sample Moisture content File bulk seed

determination sample,purity, other
varieties fraction
Registration, receiving,
weighing of submitted sample Purity Test
Check Result

Germination Test
Mixing, dividing,obtaining and
weighing of working sample Report results

Evaluating Germination
test Issue appropriate results,
tags, seals
Determination of other
varieties
To Seed inspector, seed
Other test producer
PHYSICAL PURITY
TEST

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 Physical Purity Test

Separation of Component Parts as Pure Seeds, Other Seeds and Inert Matter

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Objective
 To determine percentage composition by weight of the
sample being tested and by inference the composition of
the entire seed lot.
 To identify the various species of seeds and inert
particles constituting the sample.

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Definition
Pure Seed
 Refers to the species stated by the sender and shall include
all botanical varieties or cultivars of the species.
 Immature, undersized, shriveled, diseased and germinated
provided can be definitely identified and not transformed
into fungal sclerotia, smut balls, nematode galls.
 In graminae: Florets with caryopsis, free caryopsis and seed
unit more than half of the original size.

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Definition
Other Seed
 Refers to seed units of other plant species other than
that of pure seed

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Inert Matter
 Includes seed units and all other matters and
structures not defined as pure seed or other seed
such as:

a. Seed units that are sterile

b. Florets with caryopsis ½ original size
c. Broken or damaged seed units ½ less original size

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Inert Matter
 Unattached sterile florets, empty glumes, lemma, palea, chaff,
stem, leaves, fungal bodies like ergot, sclerotia, smut balls, sand,
soil, stone and other non-seed matter

 Leguminosae, Brassicaceae, Pinaceae with seed coat entirely

removed

 Separated cotyledons of leguminosae

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General Principle
The three components are separated as:
1.Pure Seed
2.Other Seeds
3.Inert Matter
Weighed and percentage of each part is determined by
weight
Identify seed and inert matter present

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The three components are separated as:

Pure Seed Other Seeds

(Other Crop Seeds and Weed Seeds)
Inert Matter

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 Apparatus

Sieve Seed Blower

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Apparatus

Purity Workboard

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 Forcep Petri Dish
Magnifying Glass
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Procedure
Working Sample
The Purity Analysis for rice seeds shall be 70 grams.
Weigh to the minimum number of decimal places
necessary to calculate the % of component parts to one
decimal place.

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Working Sample
Weight of Working Number of Decimal
Sample (grams) Places
Less than 1.0000 4
1.000 to 9.999 3
10.00 to 99.99 2
100.0 to 999.9 1
1000 or more 0

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Separation
 Separate sample into component parts
by seed blowers/sieves to separate light
seeds from heavy seeds.
 Repeat separation manually to identify
the other seeds and inert materials
present in the sample
 Weigh the different components in
grams.
Separating sample into
Component Parts by
Seed Blower

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 Calculation and Expression of
Results
 Results should be calculated to one decimal place.
 % must be based on the sum of the weight of
components, not on the original weight of working
sample.

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 Calculation and Expression of
Results
The sum of the weights of components must be
compare with original weight as a check of material loss
or error.
A discrepancy of more than 5% of the original weight, a
re-test must be made.

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Reporting Results
 Results shall be given to one decimal place and the sum of
components must be equal to 100%.
Components less than 0.05% shall be reported as “Trace”.
Report scientific name of other seed.
Report the kind of inert matter.

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 SEED STANDARDS
Factors Breeder Foundation Registered Certified
Seed Seed Seed Seed
Pure seed (min.) 99% 99% 98% 98%

Weed & other crop seed 0% 0% .04% .04%

(max).

Inert matter (max.) 1% 1% 2% 2%

So…
in 40kg seeds
40kg*0.98= 39,200 or 39.2 kg pure seed
=40,000-39,200
=800grams ang tahop, bato, sagbot etc..
 Routing a Sample Through the Seed Testing Laboratory

Submitted sample Moisture content File bulk seed

determination sample,purity, other
varieties fraction
Registration, receiving, Purity Test
weighing of submitted sample
Check Result

Germination Test
Mixing, dividing,obtaining and
weighing of working sample Report results

Evaluating Germination
test Issue appropriate results,
tags, seals
Determination of other
varieties
To Seed inspector, seed
Other test producer
GERMINATION TEST

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Germination is the emergence and development from the seed
embryo of those essential structures of the different seeds.

Germination Testing (Setting and Evaluation).

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Objective:
To determine the maximum germination potential of a seed lot,
which can then in turn be used to compare the quality of different
lots and also estimate the field planting value.

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 Requirements on Germination Test:
 Adequate moisture
 Favorable temperature

 Three levels of temperature

1.Minimum Temperature
2.Optimum Temperature
3.Maximum Temperature

 Suitable substratum
 Light

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Germination Methods
Source of seed
No. of seed to plant
The seeds shall receive no pre treatment
Germination media or substrate

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Paper substrates are used for the
following:

 Top of Paper (TP)

 Between Paper (BP)
 Pleated Paper (PP)

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 Top of Paper (TP)

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Between Paper (BP)

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Pleated Paper (PP)

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Duration of the Test

 varies in different species

 1st count - when majority of seedlings have reached the stage of

development wherein proper evaluation is possible

 counting of germination tests are done during the preliminary or first

counts and subsequently until the final count

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 Scientific Name Common Prescription for First Final Additional
Name Count Count directions
Substrate Temperature including rec. for
(0C) breaking dormancy

Ipomoea aquatica Kangkong BP; S 30 4 10 --

Lactuca sativa Lettuce TP; BP 20 4 7 Prechill
Lolium perenne Perennial TP 20-30; 15-25; 5 14 Prechill; KNO3
Luffa acutangula grass BP; S 20 4 14 KNO3
Lycopersicon Patola TP; BP; S 30 5 14 Preheat (500C) soak
lycopersicum Tomato TP; BP; S 20-30 5 14 in
Oryza sativa Rice BP; S 20-30; 25 4 14 H20 or HNO3 (24
Momordica Ampalaya BP; S 20-30; 30 5 9 hrs.)
charantia Lima beans BP; S 20-30; 25 5 9 KNO3
Phaseolus lunatus beans BP; S 20-30; 25; 20 4 7
Phaseolus vulgaris Mongo BP; S 20-30; 25; 20 5 8 --
Phaseolus mungo Pea BP; S 20 4 14 --
Pisum sativum Winged TP; BP 20-30; 30 4 10 --
Psophocarpus bean TP; BP; S 25 4 10 --
tetragonolobus Kudzu TP; BP; S 20-30; 20 7 14 --
Pueraria javanica Radish TP; BP 20-30 4 10 --
Raphanus sativus Eggplant TP; BP 20-30 7 21 H2SO4
Solanum melongena Sorghum TP; BP; S 15; 10 4 8 Prechill
Sorghum vulgare Spinach BP; S 20 5 8 KNO3
Spinacia oleraceae Wheat BP; S 20-30; 25 4 7 Prechill
Triticum aestivum Pole Sitao 20-30; 25; 20 Prechill
Vigna sesquipedalis Corn Preheat (30-350C)
Zea mays Prechill; GA3
--
--
Agricultural and Vegetable Seeds NATIONAL SEED QUALITY CONTROL SERVICES
 Epigeal
Germination

Growth and Development of the Seedling

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 Hypogeal Germination of Wheat (Triticum aestivum)

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Categories of Seedlings and Seeds
1. Normal Seedlings 2. Abnormal Seedlings

Damaged
coleoptile

Shoot deformed Root not sufficiently developed

or missing or totally missing

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 Categories of Seedling and Seed
Fresh Ungerminated
Hard Seeds Dead Seeds
Seeds

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A. Preliminary or First Count
Normal Seedlings
Doubtful seedlings that have not yet developed
Mold growth/deteriorated

B. Second Counts to Final Counts

Normal Seedlings
Abnormal Seedlings
Fresh ungerminated
Dead seeds

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When to Retest?
Out of tolerance
Presence of firm ungerminated seed.
Evidence that the results may not be reliable:
• Improper test condition
• Errors in seedling evaluation
• Presence of fungi and bacteria
• Inaccuracies in counting and recording results

Seedling abnormality due to chemical treatment

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Average Average
percent No. of replicates percent No. of replicates
germination of 100 seeds germination of 100 seeds
4 3 2 4 3 2
A B C D E A B C D E
99 2 5 - - 75 26 17 16 14
98 3 6 5 - 74 27 17 16 14
97 4 7 6 6 73 28 17 16 14
96 5 8 7 6 72 29 18 16 14
95 6 9 8 7 71 30 18 16 14
94 7 10 9 8 70 31 18 17 14
93 8 10 9 8 69 32 18 17 14
92 9 11 10 9 68 33 18 17 15
91 10 11 11 9 67 34 19 17 15
90 11 12 11 9 66 35 19 17 15
89 12 12 11 10 65 36 19 17 15
88 13 13 12 10 64 37 19 17 15
87 14 13 12 11 63 38 19 18 15
86 15 14 13 11 62 39 19 18 15
85 16 14 13 11 61 40 19 18 15
84 17 14 13 11 60 41 19 18 15
83 18 15 14 12 59 42 19 18 15
82 19 15 14 12 58 43 19 18 15
81 20 15 14 12 57 44 19 18 15
80 21 16 15 12 56 45 19 18 15
79 22 16 15 13 55 46 20 18 15
78 23 16 15 13 54 47 20 18 16
77 24 17 15 13 53 48 20 18 16
76 25 17 16 13 52 49 20 18 16
Maximum Tolerated Ranges in Germination Percentage
Computation:
Germination - 85%
1 grain = 0.02 g
1000 grain=20 grams or 0.02kg
2,000,000 grain=40kg
2,000,000grain x 0.98 physical purity
1,960,000 x 85% germination=1,666,000
0.20 x 0.20 planting distance=250,000 grains-1 seed/hill; 500,000-2
seed/hill;…
VARIETAL PURITY TEST

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 VARIETAL PURITY TEST

Determination of Other Varieties thru Varietal Purity Test.

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Objective
 To determine the extent to which submitted sample
conforms to species or cultivar claimed for.
 To gain information on the amount of other varieties
and identify the mixtures as much as possible.

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Definition
Other varieties
includes other kinds, varieties of rice.

Principle
 Determination is made by count and expressed as number in
percentage of seeds found in the sample examined.
 Seeds are compared with authentic samples.

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Apparatus

Purity Workboard
w/ Diaphanoscope
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Magnifying Glasses Stereo Microscope

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Forceps, Spatula, & Petri Dish
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Procedure
 The 500 grams working samples for rice and corn are
examined seed by seed.
 The number of other varieties is reported as number
per working sample.
 Other varieties are determined.

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Other Varieties
A. Seeds
 Sample is searched for other cultivars side from subject
sample but of same species.
 Separate the mixtures or other varieties
 Identify the mixtures or other varieties.

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Samples of other varieties based on:
GRAIN LENGTH

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Samples of other varieties based on:
GRAIN SHAPE
SLENDER (S) Intermediate (I)
(more than 3.0) (2.0-3.0)
NSIC Rc 280 – 3.9 NSIC Rc 272 – 2.4
BOLD (B)
(less than 2.0)
NSIC Rc 242 – 2.0

SLENDER (S) Intermediate (I)

(more than 3.0) (2.0-3.0)
NSIC Rc 238 – 3.2 NSIC Rc 240 – 2.9

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Other Varieties
B. Seedling Characteristics
 Germinate / plant seeds of other varieties together with the
authentic sample.
 Observe the seedling characteristics.

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 Calculation and
Expression of Results
Result is expressed as number of seeds per unit
weight as prescribed in the standard.

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SEED STANDARDS
Factors Breeder Foundation Registered Certified
Seed Seed Seed Seed

Other varieties, grains/500g 0 2 5 20

(max.)

Computation:
500 grams- 20 other varieties
1kg- 40 other varieties
40kg - 1,600 other varieties
SEED STANDARDS
Factors Breeder Foundation Registered Certified
Seed Seed Seed Seed
Pure seed (min.) 99% 99% 98% 98%

Weed & other crop 0% 0% .04% .04%

seed (max).

Inert matter (max.) 1% 1% 2% 2%

Other varieties, 0 2 5 20
grains/500g (max.)

Germination (min.)* 85% 85% 85% 85%

Moisture content 14% 14% 14% 14%

(max.)

*based on pure seed only.

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 SUBMISSION SEED TESTING
AND RECEIPT
FILE BULK SEED SAMPLES
OF SAMPLES
PURITY, OTHER
VARIETIES FRACTIONS

MOISTURE TEST

CHECK
RESULTS

RECORDING PURITY TEST

OF SAMPLES

REPORT RESULTS

GERMINATION TEST
PREPARATION OF
ISSUE APPROPRIATE
WORKING SAMPLES
CERTIFICATES, TAGS

Accelerated Aging VARIETAL TEST

Scarification
Test

TO PRODUCER
PROCESSOR,
SEED HEALTH TEST FARMER
OTHER TEST

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Globe: 0917-165-4556
Smart- 0910-218-9951
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