Floral Biology, Anthesis, Pollination, Selfing and
Crossing Techniques in Rice (Oryza sativa L.) 2n = 24
The knowledge of floral biology is a pre-requisite for breeding and
crop improvement work
Floral structure gives an idea of various pollination mechanisms of self and
cross pollinated crops to some extent
Floral Structure:
The inflorescence of rice is a
terminal panicle borne on a long
peduncle
The main axis of the panicle: the
primary rachis bears a number
of secondary rachis
The secondary rachis further
branches into tertiary ones which
bears a spikelet at its tip
Spikelet
Spikelet consists of two empty glumes (sterile glumes)
two fertile glumes (lemma and palea)
six stamens in two whorls and
a pistil having a single central ovule
a short slender style with two plumose stigmas
two transparent fleshy lodicules situated at the base of the spikelet
attached to the inner side of the fertile glumes represent the reduced
perianth
Lemma is rough, large, boat shaped,
strongly five nerved - apex is solid or it
may be awned
Palea is narrower than lemma and
strongly three nerved
The extended tips of the lemma & palea
are the “apiculus”.
At the time of anthesis: the lodicules
become turgid and thrust the lemma and
palea apart exposing the fertile
stamens
Lodicules help in the opening of the
floret
Floral Biology and anthesis
Blooming of spikelets starts at the apex of the panicle and proceeds
downward
Spikelets generally open on a full sunny day and the maximum blooming
occurs between 8 a.m and 11 a.m
A panicle remains in bloom for 2 to 4 days but may extend up to 7 – 10
days
Each spikelet remains open for 30 minutes and then closes
The anther dehiscence takes place immediately after the opening of the
spikelets
Receptivity of stigma is maximum during first three days after opening of
the spikelets and then gradually decreases and is lost within 7 days
Viability of pollen grains is only for five minutes
Selfing Technique
Rice is a self- pollinated crop
An hour before blooming (7 a.m.) butter paper bag is placed over the
panicle to avoid any contamination from foreign pollen and to ensure
selfing
The bag may be removed after 2-3 days
Emasculation and Crossing techniques
Emasculation is necessarily followed by controlled pollination
Emasculation is done during early morning between 6 and 8 a.m.
in spikelets due to open on the same day
Crossing techniques is differs based on the method of
emasculation
Since maximum number of spikelets open on the 3rd or 4th day of
anthesis panicles of that stage are selected for emasculation
Following methods are widely used for hybridization in rice
Methods of emasculation
Hand Emasculation
Clipping method
Hot water method
Dr. Ramiah method
Vacuum emasculation method
Cuttack Method
Brown paper method
Rhind’s method
Hand Emasculation (Removal of anthers)
Spikelets which are expected to open on the next day morning
are selected and are made to open by slightly separating the lemma
and palea and the anthers are removed with the help of forceps
Clipping method
In the previous day evening: top l/3rd and bottom
l/3rd portions in the panicle of the desired female
parent are clipped off by using scissors leaving
the middle spikelets
With the help of scissors again: top 1/3 portion in
each spikelet is clipped-off in a slanting position
Six anthers present in each spikelet are
removed with the help of the needle
Care must be taken during emasculation for not
to damage the gynoecium
Then to prevent contamination from the foreign pollen the emasculated
spikelets are covered with a butter paper bag
Next day morning (usually at 9.00 a.m.) the bloomed panicle from the
desired male parent is taken
Top portion of the butter paper bag which was originally inserted in the
emasculated female parent is now cut to expose the panicle
The male parent panicle is
inserted in an inverted
position into the butter paper
bag and is turned in both ways
in order to disperse the pollen
After ensuring the abundant disbursement of pollen the opened
butter paper bag is closed using a pin
Colored thread may be tied at the base of the panicle to identify the
crossed ones
After ensuring pollination the bag may be removed
Hot water method
Hot water emasculation is used to about the same extent as the clipping
method
Panicles in 3rd (or) 4th day of blooming are chosen as female parents.
An hour or so before blooming (i.e. normally at 7. a.m.) the panicle is
selected and under developed and opened spikelets are removed
Now the tiller is bent over (carefully to avoid breaking) and the selected
panicle is immersed in hot water contained in a thermos bottle at 40-440C
for a period of 5 to 10 minutes
This treatment causes the florets to open in a normal manner and
avoids injury
Then emasculation is done by removing the six stamens by fine
forceps or needles
Dr. Ramiah method
Panicles on the 3rd or 4th day of its blooming are selected top and lower
splikelets are removed leaving only the middle
It is covered with a wet cloth and air is blown from mouth
This facilitates opening of spikelets
After 2-3 minutes wet cloth is removed and spikelets are found to be open
Then the six anthers are removed
Vacuum emasculation method
This works on the principle of suction pressure
The spikelets tip are clipped off prior to operation
The minute pipette is to be shown at the point of clipping and pollen is
sucked in.
Six panicles can be emasculated at a time
By hand emascualtion: 100 flowers can be emasculated by a person.
With the vacuum emasculator six persons can operate and emasculate
3000 to 3600 florets/hour
Cuttack Method
The technique was developed by CRRI Cuttack
The panicle to be emasculated is inserted into hollow piece of bamboo
closed at one end and plugged with cotton wool and split cork at the
other end
The flowers thus enclosed will open within 5-10 minutes.
After opening of the spikelets the anthers are removed
Brown paper method
The panicles are enclosed in a Brown paper cover before a
couple of hours of blooming
Heat develops inside due to which the anthers extrude but do not
dehisce
This happens in 15-30 minutes then the anthers are easily clipped
off
Stigmatic surface is then dusted with pollen grains collected from
the chosen male parent
The crossed panicle is then properly tagged and protected with
paper cover which is retained in a position for 7 – 10 days
Rhind’s method
Hot water is kept in the flask and it is poured outside
After pouring out the water inside of the flask will be warm and
humid
The panicle to be emasculated will be inserted into the flask and
kept for some time
Due to high temperature and humidity the spikelets will get
opened and the anthers are exposed which can be removed with the
help of forceps
Crossing
Emasculated panicle is covered with butter paper bag - Emasculated flowers may
be pollinated next morning by
Placing ripe anthers in each floret by hand
Shaking a panicle that is shedding pollen over the emasculated panicle
Approach method: in which pollen shedding of male plant is supported in test
tube with water and bagged along with emasculated panicle in a butter paper
bag (Poehlman - 1987)
Bagging and labeling is done immediately after pollination. The labels are
tagged to the inflorescence or to the flower - thread
Date of emasculation
Date of pollination
Parentage
No. of spikelets/ panicle emasculated
Crossing ledger
For maintenance of pedigree record the basic thing required is Crossing
Ledger.
This Ledger gives the details about parentage, Season in which the
cross is made.
[Link]. Cross Number Parentage
1. XS 9801 CO 2 x MS 9804
2. X S 9802 CO 4 x C152
3. X S 9803 CO 1 x CO 4
Pedigree record
In Pedigree method: a detailed record of the relationship between the
selected plants and their progenies is maintained as a result of this
each progeny in every generation can be traced back to the F 2 plant
from which it originated such record is known as pedigree record or
pedigree
The pedigree may be defined as a description of the ancestors of an
individual and it generally goes back to some distant ancestors
Thus it describes the parents, grandparents, great grandparents so
on of an individual
Maintenance of Pedigree record: in several ways
- Must be simple and accurate
- Each cross is given a number: first 2 digits – year
and remaining digits denotes serial number of the
cross in that year
- Eg: 7911 denotes the cross number 11 of year 79
In segregating generations two systems:
Designation based on the location of progeny rows
in field – System I
Designation based on the serial numbers of selected
plants – System II
System I: the individual plant progenies in F3 and later generations
are assigned row numbers corresponding to their location in the
plot
In addition each progeny in F4 and the subsequent generation is
assigned the row number of the progeny in the previous
generation from which it was derived
Generation Number Description
F3 7911-7 Progeny in the 7th row in F3 plot
Progeny in the 4th row in F4 plot selected
F4 7911-7-4
from the progeny in 7th row of F3 plot
Progeny in the 14th row in F5 plot selected
F5 7911-4-14
from the progeny in 4th row of F4 plot
Progeny in the 3rd row in F6 plot selected
System 2: In each generation the selected plants are assigned
serial numbers within individual progenies
Each progeny or selected plant bears the serial number of all
the plants in the previous generation related to it by direct
descent
Thus the plants selected in F2 are given serial numbers of their
parents (F2 plants)
The plants selected from a progeny in F3 are given the number
of that progeny and in each generation the selected plant also
given a serial number
Generation Number Description
Progeny obtained from plant number 7 selected in
F3 7911-7
F2
Progeny from plant No.4 selected from the F3
F4 7911-7-4
progeny derived from the plant No.7 selected in F2
Progeny from plant No.2 selected from the F4
progeny derived from plant No.4 selected from
F5 7911-7-4-2
the F3 progeny obtained from the plant No.7
selected in F2
Progeny from plant No. 8 selected from the F5
progeny derived from plant No.2 selected from
F6 7911-7-4-2-8
the F4 progeny of plant No.4 selected from the F3
progeny of Plant No.7 selected in F2
In this system the pedigree of a progeny is immediately known
and one does not have to refer to the previous year record
But there are greater chances of error since more numbers are
to be recorded
In both the systems: the progenies are assigned a different
serial number when they become homozygous and are
included in preliminary yield trials
This number is given to those homozygous lines that are
included in preliminary yield trials
For keeping a pedigree record following points are important:
Only important characteristics should be recorded
Only the promising lines should be included in the record
Poor progenies may be simply marked discard
The pedigree record must be accurate
To obtain a general idea about the inheritance of characters by
studying the pedigree record
Floral Biology, Anthesis, Pollination, Selfing and
Crossing Techniques in Wheat
Inflorescence: Terminal distichous spike with tough rachis, awned or
awnless, glabrous or hairy
Floral structure
Entire inflorescence on one
culm is spike which consists of
separate group of florets
(flowers) known as spikelets
Each spikelet of common
wheat has two to five florets
The florets are subtended by
two empty scales called
glumes
Each floret consists of a flowering glume (lemma) and a thin
two loculed glume (palea)
These two glumes enclose three stamens - a single ovary with
bifurcated short styles and feathery stigmas and two small
lodicules
Floral biology
Main culm flowers first and the tillers bloom later
Flowering starts at approximately 2/3 from the base and proceeds in the
both the directions
Blooming: throughout the day - takes 3-5 days for completion
Flower opening: Between 9 a.m. to 2
p.m. and peak period is between 10 a.m.
to 1 p.m
Anther dehiscence takes place
simultaneously and
Hence the crop is highly self pollinated
(<1 % cross- pollination)
Selfing: Inflorescence is covered with a butter paper cover prior to
anthesis and undisturbed till the flower opening completed
Emasculation
Wheat is a self pollinated crop
For emasculation - 1/4 to 1/3 upper
part of spike is clipped - few basal
and immature florets are also removed
In the remaining: 5 – 6 pairs of
spikelet - the central florets are also
removed and the emasculation is
carried out in the remaining lateral
florets of each spikelet
Glumes are clipped back and
anthers are removed with fine
pointed forceps
The emasculated spike is
covered by a pollination bag
After 1 – 2 days the stigmas
are visible and the emasculated
spike is ready for pollination
Crossing
Done with the fresh pollen as pollen grains remain viable for a short
period (1 – 3 hours)
For preparing male spike: a spike showing a few protruding anthers is
removed from the male parent - Its glumes are cut without any damage to
the anthers
It is held in vertical position / stalk inserted in ground under sunlight for a
few minutes - During this process- anthers emerge out of cut glumes
The upper portion of the pollination bag on the emasculated spike is
cut with scissors
Through this opening the male spike shedding pollen is inserted
and shake over the emasculated spike by twining motion and the
bag is closed with the help of U clip
This fast process of emasculation
and pollination is common and
described as ‘go go’ method of
crossing
Two other ways to pollinate
female spikes are the twirl and
approach method
Twirl method
It is rapid and quick
Top of the bag covering the female spike is cut off and pollinating
male spike is inverted into the bag parallel to the female spike
The male spike is vigorously rotated by twirling its peduncle between
the thumb and forefinger
Approach method
The female spike is positioned slightly below the male spike and both
spikes are covered with a bag
Detached male spikes can be kept alive to shed pollen for 2 or more
days by placing their culms in water
Breeders have better success with the approach method than with the
anther transfer or twirl method
After pollination: the spike is recovered immediately to minimize
accidental pollination
Paper tags are used to record the cross number, the parents, dates of
emasculation and pollination
Floral Biology, Anthesis, Pollination, Selfing and
Crossing Techniques in Maize
Floral Biology
Maize is a monoecious plant
Sexes are partitioned into separate pistillate (ear or cob): female flower
and staminate (tassel): male flower
The main shoot terminates
in a staminate tassel
Maize is generally
protandrous
TASSEL: It is a terminal branched panicle in which paired spikelets (one
sessile and one pedicelled) are produced on both, the central axis and in the
branches
Each spikelet has 2 glumes, lemma, palea, 2 fleshy lodicules and 3
stamens and rudimentary pistil
COB: Ear bearing branch (cob) is much like main shoot - covered by the leaf
like structures called husk (bracts) having enlarged leaf sheaths forming a
protective covering around the inflorescence
The spikelets occur in pairs - lower flower is non-functional represented by a
lemma and palea
The upper one is fertile and consists of a
membranous lemma and palea and a knob
shaped ovary long thread like style called
silk
Silk functions both as stigma and style and
it is receptive to fresh pollen grains throughout
the entire length.
Lodicules are generally absent.
Anthesis
A cross pollinated crop with 95% cross pollination
The anthesis starts from tip and proceeds downward
Maize is protoandrous in which pollen shedding normally begins 1-3
days before the emergence of silk and continues 3-4 days after the
silks are ready to be pollinated
A single tassel may produce as many as 2,50,00,000 pollen grains
Pollen grains are viable for 12-18 hours
Pollen may be carried by wind upto one kilometer (Anemophily)
Fertilization occurs within 12-28 hours after the silks are pollinated
Selfing
Cover method
Bag the tassel before anthesis with a brown paper cover usually
called as tassel cover
Bagging should be done in the previous day evening to avoid
contamination
Cut the tip of the cob before the silks emerge and cover with a silk
cover - butter paper cover
After 3-4 days: the silks will emerge in the form of a
‘saving brush’
Remove the cover of the tassel containing pollen
and insert it over the cob after removing the silk
cover
Tap the tassel cover gently so that the pollens fall uniformly on all
the silks. Then insert this cover well in the cob and tie it at the base.
The tassel and cob in a plant are covered with separate paper
covers and pollen grains collected in the tassel cover are deposited on
the silk.
Usually periodical (2-3 times / day) exchange of the two covers will
ensure selfing. This is continued for 4-5 days.
The cover on the cob is retained for 2-3 weeks till the receptivity of
the silk is completely lost.
Bottle method
Just before anthesis the tassel pulled out from the plant and the stalk
inserted into a bottle containing water
The male flowers in this condition will remain alive for 2-3 days
This bottle with the live tassel is tied above the cob of the same plant
and both are covered with a single cover and retained for 2-3 days
Then tassel is removed and cob is kept covered for 2 more weeks or till
the receptivity of the silk is lost
Crossing technique
Female parent
[Link] the tassel before pollen dehiscence (Detasseling)
[Link] the tip of the cob before the silks emerge and cover with silk cover
Male parent
[Link] the tassel before anthesis begins
The details like date of pollination, parentage and breeding
programme to be carried out are clearly written by water proof
pencil
The date of pollination will be one day later than the date of
tasselling
Pollination should be completed within one week of silk
emergence
Ex. No: 3 – Sorghum and Millets
Floral Biology, Anthesis, Pollination, Selfing and
Crossing Techniques in Sorghum
Sorghum - Sorghum bicolor (2n = 20)
Origin: Originated in Ethiopia
Related species
Sorghum arundinaceum and Sorghum halepense
Floral biology
Inflorescence is usually compact or semi-compact or loose (lax) panicle
Panicle consists of paired spikelets
One is sessile and the other is pedicellate or staminate
Sessile or fertile or perfect spikelet: Bisexual or hermaphrodite and has
2 glumes (G1 & G2) and has 2 flowers inside
Lower flower is sterile with lemma
(L1) and no palea
Upper flower is bisexual with
lemma (L2), palea (P2), 2 lodicules, 3
stamens and a single ovary with 2
long styles ending in a feathery stigma
Staminate or pedicelled spikelet:
2 glumes enclosing 2 florets
Lower floret - lemma only and upper
floret - lemma, no palea, 2 lodicules,
3 stamens and pistil absent
Anthesis
Blooming starts in the upper most panicle branch and proceeds downwards
Flowering occurs prior to sun-rise or in the early morning and may extend
to mid-day under cloudy day
Six to nine days are required for a panicle to complete blooming
Anthers dehisce when they are dry (but not in heavy dew or rain) and pollen
blows through air
Stigmas are receptive before flowering (Protogyny) and receptive for 6-8
days
Pollen is viable only for a few hours under natural conditions and loses its
viability rapidly
Fertilization is completed within 2-4 hours after pollination
Sorghum is normally self-pollinated but some florets are protogyny
resulting in cross pollination averaging about 6%
Sorghum is classified
as Often cross
pollinated crop
Selfing
Head bagging becomes efficient for selfing the ear heads
Once the decision to bag heads has been made - all heads in a row
should be covered
If a head has already begun to flower -
the flowering portion should be cut off
During head bagging: boot leaf of the
plant is usually removed prior to placing
the bag
Crossing technique: Emasculation
1) Hand emasculation
Only a part of the panicle is emasculated and the remaining panicle is clipped
away
During clipping: flowered tip and the lower panicle branches are removed
About 50 florets which would normally flower the following day are selected for
emasculation
Needle is inserted at the middle of the floret and moved across the glumes
The needle is rotated at 900 and three anthers are lifted out
The emasculated panicle is covered by a suitable paper bag
2) Hot water method
Panicle flowered tip and lower panicle
branches are removed
About 50 florets (in clusters of two or three)
are immersed in hot water at 480C for 10
minutes
3) Plastic bag/ mass emasculation technique
Sorghum panicle is covered with plastic bag
This creates high humidity inside the bag
Under such a humidity: florets open - anthers emerge but shed no pollen
The anthers are knocked free of head by tapping
In this method: some selfing occurs
Marker genes are needed to identify the plants arising from selfed seed
Pollination
On a dry morning when pollen shedding occurs between 6.00 and 7.00 a.m.
the hand pollination may be done around 9.30 a.m.
In rainy days: the operation may be started at 11.30 a.m. - 12.30 p.m.
The pollen is collected in paper bags
Sorghum pollen kept in bags is viable for 10-20 minutes
For collection: appropriate heads may be selected and bagged in the previous
night itself
The collected pollen is dusted over the exposed stigmas or pollen producing
head may be brushed over an emasculated head
Pearl millet - Pennisetum glaucum (2n = 14)
Origin: West Africa
Related species:
P. ramosum (2n = 10)
P. purpureum (2n = 28)
P. orientale (2n = 18, 27, 36, 45, 54)
Floral biology
Compound terminal spike called panicle, cylindrical, peduncle thin
A rosette of bracts consists of bristles
and spikelets united at the base and
known as involucre
Each involucre may include one to nine
fertile spikelets
A single spikelet has one upper and one lower floret
The lower floret is staminate or sterile which consists
of a single lemma - 3 stamens – P1 (Palea) may be
present or absent - Lodicules absent – No ovary
Upper floret is fertile – posseses lemma, palea, three
anthers and a pistil with two feathery stylar branches
These structures are enclosed between lemma and palea
Pollination : Cross pollination takes place because of the protogynous
nature of the flower
But self pollination also takes place to certain extent
due to overlapping of female and male phases in the
same inflorescence
Anthesis
Pearl millet is a naturally cross pollinating species due to protogynous
nature
All flowers first exert stigmas 1 to 3 days earlier and fertilized by out
crossing with the help of wind
Stigmas wither about 8 hours after pollination
Self pollination can occur when stigma emergence on later flowering
tillers which overlaps anthesis of earlier head and around 20% self
pollination is reported
Because of protogyny - Blooming occurs between 10 p.m. and mid-night
The stigmas remain receptive for 1-2 days
The anthers emerge after drying of the styles
Anthers emerge in two waves
First involves the perfect flowers and Second wave commences 2-3 days
later involving staminate flowers
Pollen grains viable for 5-7 hours
Anthesis starts from the upper third of the head and proceeds towards the
base
Selfing
To ensure selfing - spikes may be bagged before emergence of the
stigmas
As the spike elongates it may be necessary to adjust the bag to cover the
lower most spikelets
Crossing
Emasculation in pearl millet is laborious and difficult due to the small size of
the flowers and the late maturity of the anthers
For cross pollination about 4/5 of the upper portion of the spike is
clipped and the left over portion is bagged
Likewise the ears of the pollen parent are also bagged
As soon as the stigmas of the female parent emerge - the entire panicle is
dusted by shaking a pollen shedding spike of the male parent
The bag of the female parent is cut along the top and the clipped earhead
of male parent is introduced into the female bag and rotated around the
ear-head gently brushing the stigmas
The bag on the female is folded down and stapled
Details of the cross, the date of pollination should be given
When the female and male parents are closer are of the same height and
synchronous in flowering - the earheads of both the parents are enclosed
in one bag for cross-pollination
This method is particularly suitable for making cross between A and B
lines
Ragi/ Finger millet - Eleusine coracana (2n=4x=36)
Origin: India
Related Species
E. indica (2n = 18)
E. brevifolia (2n = 36)
E. verticillata (2n = 36)
Floral Biology
Terminal digitate, straight or slightly curved Spikes
Spikes borne on a long peduncle from the end - four to
five spike radiate in a whorl called fingers with an odd one
a little lower down the whorl called as the thumb
Shape the inflorescence - 5 types: top curved, incurved,
fisty, open and Cocks comb
Unit of inflorescence is a spikelet and are densely packed on the side of each
rachis in two rows
The average number of spikelets in each finger is above seventy
Each spikelet contains 6 to 12 florets enclosed by two common glumes (G1
and G2) - outer small and inner large
Florets are bisexual
Each floret contains a lemma and palea with three stamens and a superior
ovary with two feathery stigmas and two broad and truncate lodicules inside
Anthesis and Pollination
In Spike: flower opening is from top to bottom
In spikelet: opening of the floret is from base to top and one floret in each
spikelet opens a day and maximum number of florets open on the third day
An inflorescence takes 7 to 8 days to complete anthesis
Anthesis takes place between 1 a.m. and 5 a.m.
As soon as the glumes and palea begin to open - the stigmas and anthers
emerge almost simultaneously and soon after the anthers dehisce and
pollinate their own stigmas
Glumes close between 7 a.m. and 8 a.m.
Selfing: Panicle before commencing anthesis is covered with paper cover and
retained till the blooming is over
Crossing
Both hand emasculation and hot water treatments are followed
Hand emasculation is done in the evening and pollination is done very early in
the morning - before 6. 0 a.m.
For hot water treatment the
panicle is immersed in water at
52oC for two minutes - then the
spikelets are pollinated early in the
morning
Approach method or contact method
Inflorescence to be opened will be selected and cut with long stalk from the
male parent
This is brought to the emasculated flower
The male flower as a whole will be tied round with female flower - then they
are covered with butter paper bag
The cut end of the male inflorescence will be immersed in water kept in a bottle
Natural cross pollination takes place in 2 to 5 days
Marker genes are utilized for identifying the hybrid seedlings in the nursery plot
60-90% seed set is recorded in both methods
Little Millet / Samai - Panicum sumatrense (2n = 36)
Inflorescence is a panicle
Panicle contracted along nodding
Primary panicle branches appressed: panicle branches scabrous, drooping at
maturity
Spikelets comprising of 1 basal sterile floret and 1 fertile floret without rachilla
extensions
Spikelets are elliptic - dorsally compressed – acute - persistent on plant – 3
anthers
Self-pollinated crop
Panicle takes 15 days to
complete blooming
Anthesis time: 9 to 11.30 a.m.
Kodo Millet / Varagu - Paspalum Scrobiculatum (2n=40)
Inflorescence of spicate (arranged in spikes) main branches - digitate
or sub digitate - non digitate
Spikelets are hermaphrodite - florets 2
Lower sterile and without stamens
Upper fertile
Lemma and palea present
Lodicules present - 2 [free, fleshy and glabrous]
Stamens 3
Ovary glabrous - styles free to their bases,
stigmas 2 and red pigmented
Self pollinated crop and it has
cleistogamous flower or
chasmogamous (open don't exceed
15-20%) with and without hidden
cleistogenes
Spikelets at the middle of spikes open
first and gradually spread to either end
Spikelets open after midnight: from
2.30 a.m. to 3.00 a.m. and continue till
sunrise
Barn yard Millet / Kudiraivali - Echinochloa colona (2n=36, 48, 54, 72)
Panicles are long, erect to slightly drooping at maturity
Spikelets often with 1 sterile and 2 bisexual florets
Spikelets are more or less crowded on the spike like branches of the panicle
Anthers 3 and are purple in colour
Order of flowering is from tip to the bottom of panicle
The total flowering period extends from 19-22 days
Anthesis - 5 am to 10 am
Peak flowering
time is 6 a.m. to 7
a.m.
Self-
pollination is the
general rule
Proso Millet / Panivaragu - Panicum miliaceum (2n = 36)
Common millet / French millet / Brown corn millet
Inflorescence is a drooping panicle
Spikelets contains two florets - lower sterile floret which is staminate or
without stamen - upper fertile floret
Stamens 3 and Superior ovary
Self-pollinated crop with more than 10% cross pollination.
Panicle takes
10 days to complete
flowering
Anthesis: 10
am to 12 pm
Foxtail Millet / Tenai - Setaria italica (2n=18)
Panicle is compound, large, heavy, dense, cylindrical lobed borne on
a very thin and short pedicel
Rachis: soft, hairy bristles, 1-3 per spikelet, central rachis frequently lax
and panicle drooping
Spikelet's bear 2 florets: lower
floret sterile and upper floret
perfect
Self-pollinated with 0 to 10 per
cent natural crossing
Anthesis
Self-pollination is the rule
Flowering proceeds from the top to downward in the main panicle and from
the tip downwards in each of the panicle branches
The stigmatic branches are the first to emerge
After that anthers emergence start dehiscing by longitudinal slits from the top
to bottom – the process takes about three minutes
After the emergence of first anther - five to ten minutes the other two are
pushed out
After pollination the
lodicules shrink and
the glumes begin to
close
Time taken for an earhead to complete flowering varies from ten to fifteen
days
From the third to sixth day of emergence a large number of flowers open
Two maximum wave of flowering: During a day - one between 10 p.m. and
midnight and other between 6 a.m. and 8.a.m.
Panicle takes 10-15 days to complete blooming
Emasculation and crossing technique in small millets
Hand emasculation is tedious because of small sized florets.
To overcome this the Russian method is followed
Method
Select the panicle which first commenced flowering
Remove the already opened florets
Rub the selected panicle in between hands to increase the temperature by 1
to 2o C for 2 minutes
Immerse the panicle in cold water
The flowers will open but anthers will not dehisce
Take out panicle from water and remove unopened flower
From opened florets remove anthers
Pollination
Collect the panicle from male parent which are in the process of
flowering
Shake the panicle on the emasculated florets
Tie the male panicle to the emasculated female panicle
Cover it with butter paper bag which was immersed in water
The water in butter paper will maintain humidity
Ex. No: 4 – Redgram and Chickpea
Floral Biology, Anthesis, Pollination, Selfing and
Crossing Techniques in Redgram
Floral Biology
Axillary or terminal raceme borne on long peduncle
The flowers are yellow or purple
Calyx tube is campanulate
Corolla is highly zygomorphic,
papilionaceous and yellow
It includes one standard petal
(Vexillum/ flag), two wing petals
and two keel petals
Stamens are 10 - diadelphous (9+1)
Stamens show dimorphism
Of the 10 stamens: four have short filaments and six have long filaments
Ovary is superior, sub-sessile, densely pubescent with 2-9 ovules
Style is long, filiform and
glabrous
Stigma is capitate
Anthesis
Often cross pollinated crop
Self pollination: Occurs in the bud before the flowers open
Cross pollination: Takes place after the opening of flower with the help of
insects
In the young buds: Stigma lies above the level of anthers - Style is so curved at
the tip - that the stigmatic surface is directed towards the anthers
As the bud develops: Filaments
elongate bringing the top five anthers
dehisce in the bud a day before the
flowers open
Self pollination takes place
Receptivity of stigma starts 68 hours before
anthesis and continues for 20 hours after
anthesis
This favours cross pollination
Cross pollination from 0 to 70% has been
observed in redgram
Selfing:
Selfing is done by covering an individual inflorescence, a branch of a plant,
or a whole plot
When a large amount of seed is required, group of plants are covered with
bee-proof cages
Bagging
Three types of selfing bags
Glassine bag (13 cm x 8cm) to cover an individual inflorescence
A small – muslin – cloth bag (60cm x 20cm) to a cover a flowering branch
A large muslin – cloth bag (135cm x 90cm) to cover an entire plant
Emasculation
Bud most likely to shed pollen the next day are selected for emasculation
Steps
Hold the bud firmly between the thumb and middle finger with support of the
index finger so that the keel of the standard is facing towards the emasculator
Remove or push down the sepal covering the keel
Open the corolla by inserting one tip of the forceps at the base of the keel
Move the forceps upward to the tip of the standard
Press the bud with a slight pressure until it opens. This makes the anthers
visible
With the forceps remove the anthers from the staminal column
Count the anthers or examine the bud with a magnifying glass to ensure
that all the anthers or their broken parts are completely removed
Pollination
Stigma is receptive before anthesis - pollination can be done immediately
after emasculation
Source buds are collected between 8.00 and 10.00 a.m.
Remove the corolla of the pollen – source bud so that the staminal
columns and anthers are uncovered
To transfer pollen: hold the flower in one hand and touch the anthers to the
stigma of an emasculated bud
A single flower can be used to pollinate two or three emasculated flowers
To identify the artificially pollinated buds small, bright – colored, thin nylon
thread is tied to the peduncle of the bud.
Seeds are harvested only from such pods
Seed is harvested at
physiological maturity 30 – 35
days after pollination
Floral Biology, Anthesis, Pollination, Selfing and Crossing
Techniques in Bengalgram
Chickpea / Bengalgram / Channa [Cicer arietinum - 2n=16]
Chickpea is a herbaceous annual with a robust and long tap root system
Floral Structure
Chickpeas have solitary papilionaceous flowers in axillary racemes
Small (is 1.5 mm long) and triangular bracts are found
Pedicels are straight when flowering and curved when
bearing fruit
Chickpea has a glabrous calyx and has five partly
joined sepals
Peduncle and calyx are hairy
Corolla is veined and may be pink, purple, red, white,
blue, greenish white in colour
Standard petal or vexillum is clawed, glabrous or scarcely pubescent and
does not have any glandular hairs
Wings are free and obovate
Keel is incurved with 2-3 mm long pedicel
Stamens are diadelpous, 9 fused stamens and the 10th stamen is free (9+1)
Anthers are dorsifixed
Pollen is orange coloured
Ovary is ovate and covered by
predominantly glandular hairs on its
surface with 2-4 ovules
Style is linear, upturned and 3 to 4 mm
long with a globose stigma
Floral Biology
Chickpea is a self pollinated crop with out crossing limited to 1.58%
Self pollination takes place one or two days before opening of the flower
Flowers open in morning and close in the afternoon and each flower opens
on two or three successive days
Developmental Stages of the Bud and Flower
Eshel (1968) identified five stages of development of the bud and flower in
chickpea
a. Closed bud: Stigma is immature and anthers are still at the base of the bud
b. Hooded bud: Corolla has elongated and the anthers are about half the height
of the style. The stigma is receptive
c. Half-open flower: At this stage the anthers attain the same height as
the stigma and the pollen mature just before the dehiscence of the anthers
Self-pollination takes place at this stage while the keel petal remains
closed preventing the entry of foreign pollen
For crossing pollen are collected at this stage
d. Fully open flower: The anthers become shrivelled while the standard
and wing petals are fully expanded. Fertilization takes place 24 h after
pollination
e. Fading flower: This is the post fertilization stage in which the ovary
begins to elongate.
Anthesis
Anther dehiscence takes place inside the bud one day before the opening of
the flower
When pollen are first liberated: the stigma is still above and quite free from the
base of the anthers
The filament gradually elongates to carry the anthers above the stigma
This process is completed before the flower opens thus facilitating self-
pollination
Anthesis in chickpea is throughout the day
Emasculation
Buds that are likely to be in anthesis after one or two days are selected for
emasculation
In such a bud (hooded bud) the anthers are not yellow
The bud to be emasculated should be held gently at the base with the
thumb and fore finger
Snip off the frontal sepal
Push the keel petal downwards by slitting it with a fine-pointed forceps to
expose the anthers
Remove the anthers and count them and also check with the help of a lens to
ensure that no anther is left in the flower
[Link].5
Floral biology, Anthesis, Pollination, Selfing and Crossing
techniques in Greengram, Blackgram, Cowpea, Soybean,
Horsegram and Lablab
Green Gram / Mung bean/ Moong - Vigna radiata (2n=22)
Floral Structure
Papilionaceous having one standard, two wings, two keels, diadelphous
androecium and a gynoecium
Gynoecium is monocarpellary with a superior unilocular ovary
The stigma is hairy and placentation is marginal
The calyx comprises of five sepals, three
large and free and two small and fused
Keel encloses the reproductive organs, 10
stamens and one gynoecium
Anthesis
Flowers open between 6 a.m. to 8 a.m. and remain open till 11 a.m.
Anthers start dehiscing by 9 p.m. and are completely dehisced by 3 a.m.
Self pollination is the rule
Cleistogamous in nature
For pollination: Staminal column having stamens and anthers intact is taken
out from the freshly opened flowers and rubbed against the stigma of the
emasculated bud
Emasculation in the evening
and pollination in the next morning
gives best results in pod set
Emasculation in the morning
and pollination in the evening of the
same day results in good pod set
Black Gram / Urd bean - [Vigna mungo - 2n=22]
Calyx includes five sepals and calyx lobes are lineage
Corolla (5 petals) is pale yellow
The standard petal is 12-16 mm wide. There are two wing and two keel
petals. Stamens 10 - diadelphous [9+1]
Style is spirally twisted
Urdbean is a highly self pollinated crop with cleistogamy upto 42%
Anthesis occurs in the early morning
hours
Hand pollination is required for achieving
desired hybrid combinations
Emasculation and pollination is done
as in greengram
Cowpea - Vigna unguiculata (2n = 22)
Floral Structure
The flower is bisexual, white, purple or pale violet
It is complete flower with five sepals and five petals
The keel petal is straight
The standard petal is whitish to violet in colour
The calyx is composed of five
sepals - gamosepalous
The two are large and three
are small which makes (2+3)
arrangement of sepals
The corolla is papillionaceous with an erect standard spreading at
the time of flower opening
The pigmentation pattern of corolla varies from white to solid mauve
with yellow spots near the base of the standard petal
The wings are adherent to the boat -
shaped keel enclosing the androecium
The stamens are diadelphous (9+1)
Anthers are bright yellow
Ovary is monocarpellary, unilocular
with many ovules
Anthesis
Cowpea flowers are large and showy
Mostly flowers open between 7 and 9 a.m.
But the dehiscence of the anthers is much earlier
It may vary from 10 p.m. to 12.45 a.m.
Because dehiscence of anthers happens before flower opening
Cowpea is self pollinated in nature
Emasculation and Pollination
Emasculation needs to be carried out in mature flower buds in the
preceding evening
After emasculation the disturbed parts of standard, wing and keel are
brought in original position as far as possible
To prevent drying out of the emasculated bud - a leaflet may be folded
and pinned around the bud
A tissue paper can be used to cover and protect the bud
Pollination is done on next morning from the freshly opened flower
Cowpea flowers are highly sensitive and drop off easily with slight
mechanical disturbance or injury
More crosses are to be effected
Soybean - Glycine max (2n = 40)
Inflorescence: Flower small, numerous upto
twelve on short racemes arising in the axils of the
leaves, white or purple
Calyx hairy, standard broad, auricled at the
base, pale coloured whitish or light purple with
deep purple veins at its base
Androecium : Stamens ten (10) Monadelphous
Gynoecium : Ovary short, hairy with short
curved style and apical stigma present above the
stamens
Pollination : Self pollination is the rule
Horsegram - Macrotyloma uniflorum
2n=24
Flowers are yellow or greenish yellow on
very short stalk
Sessile or sub-sessile, 2 to 4 flowered
axillary racemes
Calyx: Campanulate, sepals 5,
gamosepalous
Corolla: Papilionaceous, petals 5,
polypetalous
Androecium: Stamens ten, diadelphous
(9+1), filaments alternately short and long,
anthers uniform, dorsifixed
It is a self pollinated crop
Lablab - Lablab purpureus [2n=22,24]
Inflorescence is lax, fascicled of many
flowered racemes on elongated peduncles
Flowers are white or blue or purple on
short pedicels
Papilionaceous corolla with superior
ovary and persistent style and 10 stamens
(9+1)
It is predominantly self-fertilizing
[Link].6
Floral biology, Anthesis, Pollination, Selfing and Crossing
techniques in Groundnut, Sesame and Sunflower
Groundnut - Arachis hypogaea [2n=40]
Floral biology
Inflorescence is unique among domesticated plants in that it flowers above ground
but produces seeds below the soil surface
Flowers are borne on axils of leaves on primary or secondary branches and
each node has upto five flowers
However three flowers per inflorescence
Flowers are modified sessile with papilionaceous corolla that appear to
be stalked due to presence of tubular hypanthium or calyx lobe
Flower is subtended by a bract with a second bract on the inflorescence
branch
Two calyx lobes and corolla consists of 5 petals (1 standard, 2 wing, 2
keel) and the calyx has 5 sepals both are borne at distal end of the calyx tube
Standard petal is light yellow to
deep orange or rarely white
Wing is usually the same colour
as standard
Style is contained within the
calyx tube and both calyx tube and
style elongate rapidly upto 5 – 7 cm
in 24 hours prior to anthesis
Androecium monodelphous - the
staminal tube bearing five oblong
and five globular anthers
Filaments are fused for two thirds of their
length
Among the globular anthers: two are
sterile
Number usually varies in different varieties
In erect types: Sterile anthers are more
common while it may be absent in
spreading types
Anthesis
Flowering starts about 25-30 days after
seedling emergence
Dehiscence of the anthers takes place from 4
to 5 a.m. and flowers open from 5.30 to 7.30
a.m
Pollen matures 6-8 hours before anthesis
Self pollination occurs because the stigma and anthers are enclosed by the
keel
Cross pollination (ranging 0 to 6.16%) also occurs through bees
Stigma is receptive before anthesis
Pollination takes place at or near the time of anthesis
Emasculation
Emasculation of groundnut can be accomplished on warm bright days from
1.30 p.m. to 4.30 p.m.
Steps for emasculation
Select well developed bud for emasculation and remove all other buds at the
node to ensure that only one flower develops at that node
Pull the leaf down gently to expose the bud
With one hand hold the bud between your thumb and index finger
Open the standard petal with the forceps and pull down the wing petals
Keel is pulled down and held out of the way with the thumb and index finger
while all anthers along with their filaments are removed
Now return the standard petal to its original position over the stigma
Usually no attempt is made to cover the emasculated flowers for protection
from outside pollen
A small thread is put on the hypanthium of the emasculated flowers for
identification or on the stem above the bud axis
Use different coloured threads on different days to identify emasculated
buds for pollination
A record of the number of buds emasculated should be maintained for each
plant
Pollination
On the morning after emasculation the standard petal is usually expanded and
the stigma is exposed between 6.00 to 7.30 a.m
A healthy flower from the male parent is selected
Its corolla is removed exposing the anthers and pollen
Now directly squeeze the pollen on to the emasculated flower stigma or on to
the forceps and transfer the pollen from the forceps to the stigma of an
emasculated flower
After pollination: remove all the other flowers that were not hand pollinated by
breaking their hypanthium near the base
When fertilization is successful the tissue below the ovary called the
gynophores elongates into a peg carrying the ovary at its tip geotropically
into the soil
In the soil the ovary takes a horizontal position and a pod develops
Mature pods can be harvested usually 55- 65 days after the pegs
developed
Sesame - Sesamum indicum [2n = 26]
It is an erect annual herb with quadrangular stem and
heteromorphic leaves
Floral biology
Flower arise from leaf axils as solitary structure or
rarely in groups of 2-3 with short pedicel
Two nectary glands are seen at the base of the fully developed flower
Calyx is five lobed and membranous
Corolla is campanulate or tubular and bilabiate two lipped – the upper
lip of two lobes and the lower lip of three lobes
Ring of hairs are seen on the throat of the corolla
Stamens - 4: Epipetalous and didynamous
Gynoecium is with bicarpellary superior ovary.
Mostly tetralocular some times 6-10 locules are seen with many
ovules
Anthesis
On a bright clear day the flowers open between 5 and 7 a.m
In the mature flower bud: just before the flower opens - the four unripe anthers
are much below the stigma which at this stage is not receptive
Anthers begin to burst longitudinally after 4 a.m in the next day and commence
to liberate their pollen
At this time: the stigma becomes receptive
The plant comes to flowering 4 weeks after sowing
Selfing
Though sesame is considered generally as a self-pollinated crop - cross
pollination upto 65 per cent was reported
Hence - often cross pollinated - Cross pollination may occur due to wind and
bee activities
Tying with thread: Selfing can be effected by tying the corolla of the unopened
flower which is selected in the previous day evening itself
Smearing of semi-solid clay: Selfing can be done by smearing a speck of
semi-solid clay on the upper portion of tubular petals of unopened flowers
Clay while on drying does not allow the tubular petals to open
This method is cheap and less time consuming one - Not effective during rainy
days
During rainy day fevicol may be applied on young flower bud to ensure selfing
Crossing
i. Soda- straw method
Emasculation technique in sesame is
easy for crossing due to epipetalous nature
of the stamens
Flower bud which is expected to open in the next day morning is selected in the
previous day evening between 3 p.m.. and 6 p.m and emasculated by just
removing the corolla tube in which the stamens are attached
Then the emasculated flower buds are covered with a piece of soda-straw
tube bent at the top in order to avoid contamination from foreign pollen
During the next day morning between 7 and 9 a.m pollen from the desired
male parents are dusted gently on the surface of the stigmas of the
emasculated flower buds after removing the soda-straw and again covered
The un-emasculated flowers are removed in the female parent
Individual crossed flowers are tagged with coloured thread for the
identification of crossed capsules
Different coloured threads are used for different types of crosses
ii. Hand emasculation method
A longitudinal slit is made on the corolla tube on the dilated side and all the
anthers are removed
The bud is then covered – it is usually done on the previous day evening
After emasculation: next day early morning artificial pollination is done and
the straw or cover is retained for two days
The capsules are covered with cloth bags for collecting seeds before the
dehiscence
Sunflower - Helianthus annuus [2n = 34]
Cultivated sunflower is distinguished from others by its single stem and large
inflorescence
Branched types also occur in commercial fields and are often used as male
parents in the hybrid seed production
Floral Biology
The inflorescence is
heterogamous capitulum or head
Head generally show a
phenomenon called “Heliotropism”
in which the developed heads face
East in the morning follow the
movement of the sun and in the
evening face west
Head is surrounded by an involucre of bracts
It contains two types of florets: ray florets and disc florets
The florets of outer whorl are called ray florets and the other flowers
arranged in concentric rings over the remainder of the head are called
disc florets
Ray florets have vestigial styles and stigmas and no anthers.
Disc florets are bisexual
Stamens 5 - syngenesious anthers (anthers are attached but filaments are
free)
Ovary is single, inferior, bifid stigma, single ovule on basal placentation
Anthesis
Sunflower is highly cross pollinated
crop mainly through insects
(Entomophily)
Flower opening starts from outer side
of the head and proceeds towards
centre
Head takes 5-10 days for complete blooming depending on size of head
Anthesis occurs between 5 and 8 a.m. and Pollen viable for 12 hours
Stigma is receptive for 2-3 days
The staminal filaments elongate rapidly and the anthers appear above the top
of the corolla
Anthers dehisce early than maturity of stigma (Protoandry)
Selfing
The unopened heads are selected and covered with muslin bag
Crossing
i. Hand Emasculation
Emasculation is done in the early morning by removing the anthers of the disc
florets in 2 to 3 whorls with forceps and the other florets in the head are removed
About 9-10 a.m the pollen from desired male parent are collected and dusted on
the emasculated head
This process is continued for 2 to 3 days
ii. Without emasculation
In sunflower head emasculation is difficult
Considering this difficulty - the heads are pollinated without emasculation
On the basis of hybrid vigour - plants are distinguished from the selfed
plants
The presence of marker genes for identifying hybrids is also utilized
effectively
iii. Chemical induction of male sterility
This achieved by spraying of 100ppm GA (Gametocide) during bud-initiation
stage consecutively for three days in the morning
Pollination
Pollination is carried out by collecting pollen from heads which are already bagged
prior to flowering
Pollen may be collected from flowering heads into paper bags by a light tap of
the hand on the base of the head.
Pollination is done in the morning by applying the freshly collected pollen by a
small piece of cotton, a hair brush or through fine cloth bag
After each cross: care must be taken to avoid contamination by wiping the hands
with alcohol
Floral Biology, Anthesis, Pollination,
Selfing and Crossing techniques in
Cotton, Jute and Mesta
Cotton
Species of cotton under cultivation are:
Diploid cotton
1. Gossypium arboreum L. (Karunganni cotton) 2n=2x=26
2. Gossypium herbaceum L. (Uppam cotton) 2n=2x=26
Tetraploid cotton
3. Gossypium hirsutum L. (American cotton) 2n=4x=52
4. Gossypium barbadense L. (Egyptian cotton) 2n=4x=52
Cotton is herbaceous annual grown in tropical and sub-tropical
regions
Branches are dimorphic in nature - lower zone (nodes) having
vegetative branches (monopodial braches) and the upper zone with
fruiting branches (sympodial branches)
Floral Biology
Flowers simple, solitary, yellowish to cream
in colour
Epicalyx 3, deeply serrated and persistent
They completely enclose and protect the tender growing flower parts called
squares
Calyx 5, corolla 5,
white or yellow or red in
colour
The petals turn pink or red the day after pollination and later fall from
the plant
Anthers are numerous and reniform
Ovary superior, penta carpellary with 3-5 lobed stigma.
Ovules many in axile placentation
Anthesis
In cotton, flowering starts from the base and proceeds towards the tip
(i.e. acropetal and centrifugal).
It takes 21-25 days for the flowers to open after the recognition of
squares.
The time of anthesis is between 8 and 10 a.m. The flowers will remain
opened till evening.
Pollen is shed directly on the stigma when the anthers open and hence
self pollination is the rule.
In cotton, the stigma is receptive for 7 hours while the pollen
viability is upto 24 hours.
Fertilization is completed in 36 to 40 hours after pollination. But
cross pollination to the extent of 5-30 % is possible by insects,
mostly honey bees.
Hence cotton is classified as often cross pollinated crop.
Selfing
•Sealing method
A mature flower bud is selected and the corolla is tied with a piece of thread.
In order to keep the threads in position, a bit of wet clay is applied over the
knot, which will avoid contamination of the stigmatic surface by foreign
pollen.
•Paper cover method
A small paper cover is put over the mature flower bud before anthesis and
kept for 2-3 days.
Hybridisation
Emasculation
The corolla is cut away with small scissors or a curved scalpel and the
anthers are removed or a narrow cut is made at the lower portion of flower
bud and corolla is carefully peeled off along with staminal column.
Care should be taken not to injure the ovary. After emasculation, cover
the flowers with paper covers.
•Scrapping method
A mature flower bud is selected from which the corolla is removed by making
a circular cut at the base.
Then the anthers are scrapped off with a forceps or scalpel by holding the
flower in horizontal position.
The emasculated flower is protected with a cover and in the next morning
artificial crossing is done by crushing mature anthers collected from the chosen
male parent on the stigmatic surface of the female parent.
•Soda straw method
The upper part of the corolla is removed from the mature flower bud by
making a circular cut at the top.
Then a small piece of soda straw is inserted over the stigma, so that the
stigmatic region is separated from the anthers.
The tip of the straw is bent to close the opening.
Next day morning, a few mature anthers collected from the male parent are
crushed and dropped into the soda straw and cross-pollination is effected.
•Doak’s method
Emasculation is done by removing the staminal column by giving a shallow
cut at the base of the bud with thumb nail and removing corolla and anther
column in one jerk twisting action.
Emasculation is done in the evening usually a day before flower opening.
Immediately after emasculation the flower is covered with colour butter
paper bag for easy identification on the next day morning.
Pollen from the male flower is dusted on the emasculated flower by rubbing
the staminal column of male parent.
Immediately after pollination the flower is covered with white
butter paper bag and proper labelling is also done.
Pollination is usually done a day after emasculation.
•Surat method
This method is useful for emasculation of diploid flowers where the top
portion of flower bud is pinched off using thumb and first finger nails by hand so
that the tip of stigma get slightly exposed and the bud is covered with mud.
As the buds mature, the stigma tip extend sufficiently for enabling pollination.
In genotypes where stigma tip excertion is comparatively low, instead of
cutting the top portion of corolla, the entire corolla is removed and lint dipped in
mud is applied on unopened anther sacs.
The pollen is applied next day morning (Mehta et al., 1983).
It is an easy method of emasculation for diploid flowers though chances
are there for selfed seed production.
Hence production of hybrids with high genetic purity (90%) cannot be
guaranted.
Floral Biology, Anthesis, Pollination, Selfing
and Crossing techniques in other oilseed
crops
SAFFLOWER - Carthamus tinctorius (2n=24)
Related species
The genus Carthamus contains about 25 valid species but only one
Carthamus tinctorius is commercially cultivated
C. palaestinus, C. oxycantha and C. creticus have basic fatty acid
composition similar to cultivated safflower
C. lanatus is resistant to rust and C. palaestinus is used as source of
dormancy
Floral Biology:
The flowers are borne terminally on the main stem, primary
branches, secondary branches and tertiary branches (if present)
These flowers consist of a group of small individual flowers
called florets
All these florets are collectively known as inflorescence
Head or Capitilum homogamous:
outer involucral bracts ovate – oblong
inner involucral bracts oblong-
acute
Florets are tubular, light yellow to orange red in colour,
hermaphrodite, bracts and bracteoles of each floret modified into thin
soft hairs
Calyx absent, corolla long, tubular, stamens five, epipetalous,
syngenesious
Ovary inferior, bicarpellary, single celled, single ovuled, basal or
ascending in placentation sometimes a few of the marginal florets are
sterile
Hand emasculation
Healthy capitula of the parental plants to be emasculated are chosen and
are bagged before any florets are opened and labeled on their penduncle
A day before anthesis the head is cleared by removing upper envelope of
the involucral bracts in order to expose the young florets
The anther tube surrounding the stigma and style is carefully
punctured at the bottom and a long narrow cut is given vertically and the
entire anther column along with the surrounding corolla is removed.
During the operation some pollen grains may adhere on the style region
which are immediately brushed off and washed by a jet of water
A convenient number of florets are emasculated, washed and examined
with a lens for any sticking pollen and then the capitulum is bagged
These emasculated florets are hand-pollinated on the next morning with
the pollen from desired plant when fresh pollen is available and the head is
again bagged
NIGER - Guizotia abyssinica (2n=2x=30)
Related species:
The genus Guizotia comprises of six species:
G. abyssinica
G. scabra
G. arborescens
G. reptans
G. villosa
G. zavattarii
Floral Structure
The inflorescence of niger is capitula or head with two types of florets:
ray florets and disc florets
The flowers develop from leaf axils in clusters of 2 to 5 capitula
(heads)
The capitulum consists of eight to 15 sterile ray florets on the periphery
of the capitulum
They are sessile,
zygomorphic, unisexual,
pistillate, ligulae, epigynous and
yellow
The ray florets are generally female but often neutral and yellow to
orange colour for attracting insects for pollination
Disc florets: hermaphrodite, usually 45 – 65 per capitulum arranged
in three circular whorls in centripetal order from periphery
They are sessile, bisexual, complete, actinomorphic, epigynous,
corolla, gamopetalous, pale yellow tubular
Consists of 5 petals fused together
forming tube like structure with a distinct
upper section surrounding the style and
stamens and lower section surrounding
the ovary
Androecium: five stamens which are epipetalous, syngenesious
with long filament and basifixed anthers
Anthesis and pollination
Highly cross pollinated crop - entomophillous
It is protrandrous with sporophytic self incompatibility
The opening of flower starts from the outer whorl first and the
process continues inward towards center of the floret
Unfurling of ray florets is visible with flowering proceeding
concentrically over a period of 8 days
For complete flowering of the crop minimum 8 to 12 days is
required
Selfing
Selfing is a difficult process in niger
Very high inbreeding depression upto 91% is observed
When flower initiation takes place: the selfing or sib mating is done by
covering two or more representative adjacent plants in a line by muslin
cloth bag or nylon mosquito net bags to exclude the insects
The shaking of bags or bagged plants is done on alternate days to
ensure pollination at maturity
Crossing (Sujatha and Angadi, 1989)
The disc floret of female parent is selected
In the disc floret stamens are epipetalous and syngenesious.
At the time of opening of flower around 8 am: the disc florets appear
swollen and turn yellow.
The anther column becomes more conspicuous with white tip.
At this stage: the white tip of anther is pulled out with quick jerk using a
fine tweezer without splitting the anther column and without damaging
the stigma
The emasculated floret is pollinated immediately with pollen
The pollinated disc floret is then bagged. After seed set the bag is
removed
Isolation distance is one kilometer for niger
MUSTARD (Brassica sp.)
In Asian countries: the commonly grown rapeseed-mustard belongs to five
different species of Brassica and one species Eruca sativa
Only [Link] is grown for condiment purpose and the other five are oil
yielding types
Species Form /variety Common name Chromosome Mode of
number pollination
[Link] - Black mustard 16 Cross
[Link] [Link] Annua Summer turnip rape 20 Cross
Biennis Winter turnip rape 20 Cross
Toria Indian rape 20 Cross
Yellow sarson Rapeseed 20 Self
Brown sarson Brown sarson 20
-tora type Self
-lotni type Cross
Eruca sativa - Rocket, taramira 22 Cross
[Link] - Rai, brown or oriental 36 Cross
mustard
[Link] - Ethiopian mustard, 34 Cross
Abyssinian mustard
[Link] L. ssp. annua Summer rape 38 Self
oleifera biennis Winter rape 38 Self
Selfing
Selfing is usually carried out by enclosing a flowering branch in a muslin
cloth bag in case of amphidiploids species which are self compatible (self
pollinated too)
In case of self incompatible diploid species: selfing is done mostly by bud
pollination
Crossing
A flowering branch whose open flowers / young pods have been
removed is bagged by muslin cloth bag
After a few days the bag is removed temporarily and pollen from
freshly opened flowers is applied on the stigma of young buds which
are preferably emasculated
The self-incompatibility in Brassica is of sporophytic homomorphic
type under monofactorial polyallelic series where pollen is inhibited on
the stigma
Techniques for temporary break down of self incompatibility (De
Nettancourt, 1972)
Bud pollination
Delayed self-pollination
Grafting
Heat – shocks
Application of CO2
Hormones and protein inhibitors
Chronic irradiation
Acute irradiation of styles
Acute irradiation of PMC
Castor [Ricinus communis - 2n =2x= 20]
Origin: Africa
Castor is tall, annual or perennial growing shrub with palmately lobed
leaves with serrated margin
Inflorescence : Monoecious - flowers in a terminal panicle with female flowers in
the upper part and male flowers at the base
Male flower - perianth five - stamens many
Female flower - ovary superior, tricarpellary, style short and branched trifid or bifid
COCONUT [Cocos nucifera] (2n=32)
Origin: Indo Pacific region
Coconut belongs to a monotypic genus Cocos, with a
single species nucifera and hence there is restricted
genetic base with no known wild or domesticated
relatives.
There are two types
1. Tall coconut (Cocos nucifera var. typica)
2. Dwarf coconut (Cocos nucifera var. nana)
Inflorescence : Compound spike, young inflorescence
enclosed in spathe, hence called as spadix.
Spadix long, stout, but later drooping branched.
More pistillate inflorescence at the tip.
Flowers are monoecious staminate flowers have bracteole, 6
perianths in two whorls, 3 in each outer perianth are shorter.
Male flowers : Stamens 6, anthers linear, dorsifixed, erect, filament short,
pistil rudimentary
Female flowers : Two bracteoles, sepals six in two whorls persistent,
ovary large, tricarpellary, syncarpous unilocular, two of three the
carpels aborted. Three sessile stigmas.
Pollination : Cross pollinated.
There are three botanical varieties of Cocos nucifera: '
Tall - Cocos nucifera var. typica:
Hardy type with the life span of 80 to 90 years. It has long and straight trunk
growing to a height of about 15 to 18 meters
The nuts mature within a period of 12 months after pollination. The copra, oil
and fibre are of good quality
Variety is cross pollinated - male flowers open first and female flowers are
receptive one week after male flowers open
Eg: West coast call, East coast tall, Kappadam, Andaman Giant, Laccadive
Ordinary.
Semi tall - Cocos nucifera var. javanica: This is self pollinated because of
overlapping of male and female phases.
Dwarf type - Cocos nucifera var. nana:
Characterized by its short stature and
earliness in bearing. Life span is less than
tall. The endosperm not suitable for oil
extraction. Self pollination because of
overlapping of male and female phases.
Eg. Chowghat dwarf, Gangabondam
Hybrid palm: The promising hybrid combinations are Tall x Dwarf and
Dwarf x Tall. Hybrids come to flower in four years and perform better in
productivity in form of number of nuts per palm and uniformity in bearing.
Tapping for toddy or sugar: Tapping in coconut is performed in the
inflorescence before the flowers fully develop. The fresh tapped juice is the
neera (padhaneer), and when allowed to ferment it is the toddy and when
fresh juice is evaporated, yields unrefined sugar known as jaggery