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M.Sc. THESIS
APRIL 2007
AGRO-M ORPHOLOGICAL CHARACTERIZATION OF SORGHUM (Sorghum bicolor.
(L.) M OENCH) LANDRACES FROM M ETEKEL ZONE,
BENSHANGUL GUM UZ REGION
APRIL 2007
AKNOWLEDGEMENT
1 would like to express my sincere and deepest gratitude to my advisors Drs. Hussein
Mohammed and Dr. Tesfaye Tefera, for their guidance, professional assistance and valuable
criticism from the inception o f the proposal up to the final write up o f my thesis.
I want to express my gratitude to the Ethiopian Institute o f Agricultural Research (EIAR) for
supporting my M.Sc. training. The support I was offered from Pawe Agricultural Research
Center (PARC) in terms o f provision o f experimental site, conducting my experiment and
other services rendered is greatly appreciated.
I would like to extend my sincere appreciation to Mekonnen Abebe, Dr. Kiros Meles,
Teramage Tesfaye, Mulugeta Tsedalu, Agdew Bekele, Yemane Tsehaye, Tamene Yohanes,
Birtukuan Fikadu and Firehiwot H/Mariam for their encouragement and support while I was
conducting my thesis research and during the writing up o f my thesis.
My sincere gratitude goes to my wife W/o AJemtsehay Eyasu, who has been handling my
family and personal affairs during my stay at Awassa and who typed this manuscript. She,
indeed, has been the backbone for my study.
Above all, my deepest thanks and gratitude goes to the Almighty God who gave me the
courage and strength to accomplish my mission. It is not possible to mention every one who,
in one way or another contributed to this work, but all o f them deserve my gratitude.
The author,
Wasihun Legesse
1
DEDICATION
This thesis is dedicated to my father Ato Legesse Getahun and my mother W/o Emuhay Kasse
for nursing me with affection and love and for their limitless support, which gave me success
in life.
II
LIST OF ABBREVIATIONS
PV Phenotypic variance
GV Genotypic variance
CV Coefficient o f variation
h2 Heritability
III
Table of Contents
Page
A C K N O W LED G EM EN T--------------------------------------------------------------------------- 1
D E D IC A T IO N ------------------------------------------------------------------------------------------II
LIST OF A B B R IV A T IO N S ------------------------------------------------------------------------HI
TABLE OF C O N T E N T S --------------------------------------------------------------------------- IV
LIST OF F IG U R E S ------------------------------------------------------------------------------------- IX
A P P E N D IC E S ------------------------------------------------------------------------------------------- X
A B S T R A C T --------------------------------------------------------------------------------------------- XI
1. INTRODUCTION -------------------------------------------------------------------------------------- 1
2. LITERATURE R E V I E W ---------------------------------------------------------------------------- 4
IV
2.5.2.5 Seed characters----------------------------------------------------------13
G erm p la sm --------------------------------------------------------------------------------- 14
3.3.2 D a ta C ollected----------------------------------------------------------------------- 27
V
4 . 1. 1 Grain c o l o r -----------------------------------------------------------------------------38
6 . R E F E R E N C E S ---------------------------------------------------------------------------------------------89
7. A P P E N D IC E S --------------------------------------------------------------------------------------------- 97
8 . B IO G R A P H Y --------------------------------------------------------------------------------------------- 104
VI
LIST OF TABLES
Page
Table 5. The observed range o f variation in morpho- agronomic characters ----- ---------------- 49
Table 6 . Means, variance components, PCV, GCV, h“, GA, and GA % for 18
Table 9. Phenotypic direct effect (bold), and indirect effect of seven traits
Table 13. Summary o f discriminant analysis for 100 sorghum genotypes using
grain c o l o r ---------------------------------------------------------------------------------------------- 76
Table 14. Group means o f 21 traits o f white, brown and red colored
VII
Table 15. Variables ordered by absolute size o f correlation within function
Table 17. Group means o f 21 traits of loose, very loose and compact
Table 18. Variables ordered by absolute size o f correlation within function for head
compactness classification----------------------------------------------------------------------83
List of figures
page
Figure 1. Frequency distribution o f grain color for 100 gen otyp es------------------------ 39
Figure 3. Frequency distribution o f head compactness for 100 gen otyp es---------------43
IX
Appendices
Page
X
Agro-M orphological Characterization of Sorghum (Sorghum bicolor (L.) Moench)
LandRaces from M etekel Zone, Benshangul Guinuz Region.
BY
VVasihiin Legessc (BSc)
Research advisors:
Hussein Mohammed (PhD) - major advisor
Tesfaye Tefera (PhD) — co~ advisor
A b strac t
Ninety two sorghum genotypes collected from Metekel Zone o f Benishangul Gumuz, western
Ethiopia and 8 checks were tested in a 10 x 10 simple lattice design. The objectives o f the
study were to determine the extent and degree o f variation in morpho agronomic characters,
to evaluate the genotypes fo r yield and yield associated traits to identify superior accessions
that can be used by the breeding program. Two row plots each 5 meters long, with a spacing
o f 0.75 x 0.15 m (a plot area o f 7.5 nr) was used. Frequency distribution o f the landraces in to
different categories o f qualitative trails indicated that artificial selection that favored straight
headed genotypes with white seed and awnless glumes with straight has been practiced.
76.5% o f the accession had white seeds, 15.5% had red and 8% had brown seeds. Awn less
genotypes constituted 92.5% o f the studied material; only 7.5% had owned glumes. About
97 % o f the genotypes had straight heads; only 3% were goose headed and these are all
checks. On (he other hand no selection seems to have been practiced for head compactness.
The proportion o f loose, very loose and compact headed genotypes was 32%), 29% and 39%,
respectively. A NOVA o f 20 quantitative traits revealed the existence o f highly significant
variation among the evaluated accessions for all traits. The phenotypic and genotypic
coefficients o f variation were high ( 20%)) fo r head weight, number o f seeds head, grain
yield plant, panicle exertion and grain yield in kg ha. Iligh heri(ability in broad sense ( 70%)
was recorded fo r all (rails except leaf width (51%)) and head width (64%), lodging (37%) and
stalk borer attack (66%). High genetic advance as percent o f the mean ( 20%) was observed
fo r leaf area (24.9%), internode length (30.7%)), stalk diameter (25.6%), head width (26.6%),
head weight (42.2%)), thousand seed weight (24.85 %), stalk horer attack (25.6%) and lodging
(87.3%). When heri lability and genetic advance as percent o f the mean were simultaneously
considered both were high fo r number o f seeds plant, grain yield plant, grain yield in kg ha,
leaf area, internode length and thousand seed weigh / indicating the presence o f additive gene
effects and possibility o f a wide scope for improvement o f these traits. Genotypic and
phenotypic correlation coefficient estimates indicated that grain yield plant was strongly
associated with head weight, yield in kg ha, number o f seeds head and thousand seed weight
both at genotypic and phenotypic levels. Path coefficient analysis revealed that number o f
seeds head and thousand seeds weight are the most important traits that should be considered
during selection for high grain yield in (he sorghum genotypes studied. The clustering o f
genotypes based on 18 traits revealed (he existence o f divergence among genotypes. Ten
distinct clusters were formed. Crossing o f superior accessions from distant dusters is
expected to give high yielding progeny. Discriminant analysis showed that genotypes with
loose head and white seed are late in maturity, taller and give more yields as compared to
compact headed genotypes with red seeds indicating to the possibility o f using qualitative
trails in selecting fo r quantitative trails.
XI
1. INTRODUCTION
Sorghum (Sorghum bicolor (L ) Moench) is one o f the major food and feed grains o f the
world. It is used as a staple food in semi arid tropical Africa and Asia. Sorghum is adapted to a
wider range o f climatic conditions than other cereal crops and it is the most important crop in
the dry low lands where rainfall is not reliable both in amount and distribution (Brhane, 1982).
Because o f its tolerance to drought, sorghum is the crop o f choice for dry regions of the world
and in areas with low rainfall. It also withstands temporary water logging conditions and can
Like other C 4 plants, sorghum has high yield potential comparable to rice, wheat and maize
and its yield could exceed 110 q/ha with average yields ranging from 7000 to 9000 kg/ha
where moisture is not a limiting factor (House, 1985). In Ethiopia, sorghum is a major crop
both in terms o f production and area cultivated. About 1.4 million hectares o f land is put to
sorghum production every year which contributes our 1.7 million metric tones to the national
Sorghum is believed to have originated in the north east quadrant o f Africa, around the
Sudan/Ethiopia border (Dogget, 1988; House, 1985). Much o f the genetic variability o f the
crop is still available in the area o f its first domestication (Africa) and in regions o f early
introduction (Asia). Sorghum is the major staple cereal in Western and Northwestern parts o f
Ethiopia, a region within the area of origin/domestication o f the crop. The area is endowed
with variety o f both cultivated and wild forms o f sorghum. Ethiopia is characterized by a wide
range o f agio climatic conditions and is home to different types o f crops including sorghum.
2
There is high genetic diversity in sorghum in Ethiopia with several pockets o f geographical
isolation. The current number o f indigenous sorghum germplasms contained in the gene bank
stands at about 6000 and represents a wide array o f diversity in the major sorghum growing
areas o f Ethiopia. This could sen/e as valuable genetic base for breeding and improvement o f
the crop in the country and the world at large (Brhane, 1973). Highly desirable genetic
characteristics were identified in some o f the Ethiopian materials and were utilized in breeding
programs extensively elsewhere in the world (Melaku, 1988). The wealth o f genetic variability
in the Ethiopian germplasm has been and will continue to be useful sources o f economically
important traits.
Though it is well known that Ethiopia possess diverse forms o f sorghum (Melak Hail, 1975),
the extent and distribution o f genetic variability o f the crop in different ecologies has not been
properly studied (Melake Hail, 1988). One o f the potential areas is the Metekel zone in north
western Ethiopia. The zone lies within the area of sorghum domestication and as such is rich
in genetic diversity o f cultivated sorghum and its wild forms. Because o f its unique agro
ecological setting, warm humid climate, the area is rich with special class o f germplasm
In order to make any genetic advance in yield, to bring stability in tolerance to different biotic
and abiotic stresses or to effect changes in crop characteristics and meet certain consumer
requirements, a breeder usually depends on the variability that is present in this germplasm
documented so that well defined sets o f samples with specific combinations o f desirable traits
can easily be retrieved and used in breeding programs (Brhane, 1982).
Although very tall (4 m or above), late and difficult for harvesting, sorghum landraces from
Metekel area are tolerant to grain mould and some are tolerant to striga. Many improved
varities released for other areas often failed to adapt to Metekel condition primarily due to
high incidence o f grain mould which is associated with prolonged rainy season, high humidity
and high temperature. However, majority o f the local materials are less prone to attack by this
and other leaf diseases and hence form good sources o f resistance. Therefore, there is pressing
need to systematically evaluate and characterize these materials so that they can readily be
incorporated in the breeding program to develop varieties adapted to the area. Variability in
plant height and other characters has been observed in the landraces o f this zone. With the
intention o f getting varieties which fit to the area a large collection o f landraces was made
from this zone. This study was conducted in order to measure the level o f variation in morpho-
2. Evaluate genotype yield and yield associated traits among the collections.
3. Identify sorghum accessions that are superior in desirable agronomic character for
2 LITERATURE REVIEW
Ethiopia is believed to be the center o f origin and/or diversity for several globally important
crop species (Zewdie, 1994). Thirty-eight crop species have been identified with Ethiopia as
primary or secondary gene center; 11 crop species have been identified having their center o f
diversity in the country. Ethiopia is a center o f origin and/or diversity for crops such as tef
(Eragrostis tef), coffee (Coffea arabica ), barley (Hordium vulgctre), sorghum (Sorghum
bicolor ), durum wheat (Tritcum durum), noog ( Guizotici cibyssinicci), sesame (Sisamum
indicum ), caster bean (Ricinus comminus), Enset (Ensete ventiricosum) and chat ( Catha
The genus sorghum is highly diverse and comprises five sections (Gaber, 1950). These are:
Harlan and de Wet (1972), section sorghum includes (1) S. hcilepense (L.) Pers., a tetraploid
rhizomatous species, and (3) S. bicolor (L.) Moench, a diploid (2n=20) annual species.
crop with an outcrossing ratio o f 5-30 % (Ell strand and Foster, 1983; Doggett, 1988). Harlan
and de Wet (1972) classified Sorghum bicolor species into five basic races (bicolor, caudatum,
5
gunea, dura and kafir) and 15 derivative races o f the basic races. All the basic races except
kafir, are present in Ethiopia (Harlan and de Wet, 1972). The classification was based on
Purseglove (1985) has tried to elucidate that the wide agroclimatic conditions o f Ethiopia has
contributed to the present biological resource o f the country. The evolutionary history o f
Ethiopian cultivated sorghum has been examined and documented (Stemler el a /., 1977).
Sorghum exists in tremendous diversity throughout the growing areas, which contain pockets
o f geographical isolation, with extremely broad and valuable genetic base for potential
breeding and improvement work in the country and the world at large. Ethiopian sorghum
germplasm is also noted worldwide as a source for useful genes such as high lysine content,
cold tolerance, good grain quality and disease and insect resistance (Doggett, 1988; Yilma,
1991).
Based on their adaptation zones within the country, cultivated sorghums are grouped in to
highland, intermediate & lowland sorghum (Alemayehu, 2003). This classification has been
made largely based on altitude, length o f growing period and amount and distribution o f
rainfall (Yilma and Abebe, 1987). Intermediate zone sorghum grows at an altitude range o f
1600-1900 masl and those o f lowlands grow in areas o f altitude less than 1600 masl.
6
The progenitors (wild sorghum) o f cultivated sorghum are widely distributed across many
African countries, including Ethiopia (Amsalu cl c i l 2000). It was further noted that wild
sorghum in Ethiopia is rapidly disappearing, largely because more and more o f its habitat is
There is a great diversity within the sorghum crop. This variability is partially the result o f the
interaction o f agricultural man with the crop plants (Doggett 1988). The enormous diversity
existing in the cultivated sorghum and the improvement that has been made by plant breeding
have been reported (Abebe and Yilma 1988; Ready et a\.., 1990). Brhane (1979; 1982) and
Doggett (1991) have discussed that much o f the genetic variability is still available in the areas
of the first domestication o f the crop (Africa) and the regions o f early introduction (Asia) both
in the cultivated species as well as the progenitors o f the crop. Considering the presence o f the
greatest variability o f the wild and the cultivated sorghum in the north - east quadrant o f
Africa, scientists are in agreement to accept Ethiopia as origin o f the crop. Doggett (1988) has
emphasized that greatest variability in sorghum is found in the Ethiopia -S udan region o f the
The diversity in Ethiopian sorghum is a result o f the unique topographic and geographic
location o f the counti'y and its complex social history (Stemler and de Wet, 1977). In view o f
this, they have examined and documented the evolutionary history o f Ethiopian sorghum.
Similarly Engles and Hawkes (1991) have suggested that the Ethiopian sorghum may well be
7
the most valuable o f the crops grown in the country, which reflects the wide variation in the
environments in which the crop is being cultivated. Brhane and Yilma (1978) have tried to
elucidate the presence o f wide diversity o f sorghum in all regions o f Ethiopia though the level
It was reported that the Ethiopian sorghum germplasm shows extensive variation for disease
resistance, panicle size and panicle type, seed size, seed color, plant height, maturity, grain
yield and forage yield and tillers (Brhane and Yilma, 1978; Yilma 1991). Based on these
studies many promising varieties have been identified and further used in the national
The wide range o f environmental conditions under which sorghum is produced in Ethiopia has
given rise to tremendous range o f genetic variability (Dogget, 1988) but the indigenous
germplasms o f sorghum has been threatened due to a series o f adverse rainfall situation, which
is forcing farmers to shift to short season crops like te f (Eragroslis tef) and early maturing
uniform sorghum cultivars. Such decisions o f farmers in the process o f planting, managing,
widely used in the evaluation and study o f genetic diversity o f crops (Agong el a l ., 2 0 0 0 ).
Morphological characteristics have traditionally been used as basis for classification. Since the
early days o f taxonomy, an overwhelming reliance has been placed on morphological traits to
8
produce practical classification. Observation and studies o f phenotypic traits are the basis for
Vavilov’s determination o f centers o f diversity for various crop species. In order for the plant
agronomic and morphological traits is imperative (Andersen and Fairbanks, 1990). Hence
morphological expressions o f any genetic constitute have been demanded for the identification
Diversity studies using morphological markers that are highly heritable traits such as seed
color, seed size, leaf color, flower color etc., are inexpensive, simple and rapid to score.
However they have weakness since many genes, that control many o f the traits can only be
determined at the whole plant level and only dominant alleles are visible morphologically
physiological level because the structural difference in the gene product may not alter its
impractical and also these traits have the disadvantage o f being influenced by environmental
factors (Andersen and Fairbanks, 1990). The pattern o f variation measured by means o f
markers, such as morphological and biochemical markers could give an insight into
evolutionary ibrces responsible for maintaining genetic variability and may also assist in
Doggott (1988) and House (1985) showed the presence o f substantial amount o f variability
among sorghum genotypes for different agronomic traits like field emergence, days to
maturity, time to flowering. The genes controlling duration o f growth determine the number of
leaves and the number o f nodes, produced before the plant flowers (FAO, 1972). It is well
known that the crop is grown over a wide range o f area both north and south o f the equator.
The objectives o f a breeder to increase and stabilize grain yield under rain-fed agriculture can
be achieved by matching crop duration and the length o f the growing season as determined by
soil temperature and moisture. With respect to this, the FAO (1972) emphasized that the
temperature and photoperiod. The variability o f sensitivity to photoperiod among cultivars and
According to Vanderlip (1979), time required from planting to half bloom depends on the
maturity period o f the plant and environmental conditions. Doggett (1988) has examined
aspect o f this and suggested that flowering among sorghum may spread over a period o f 6 to
15 days depending on the size o f the head, temperature and the variety. Periods o f 6 to 9
weeks after emergence are common for sorghum to begin flowering. House (1985) has
discussed that sorghum usually flowers in 55 to 70 days in warm climate but this may extend
According to Doggett (1988) mature sorghum leaves may reach a width between 1.5 and 13
cm at widest point, while House (1985) reported this to be 10 to 15 cm. Like-wise the leaves
vary in length, ranging from 30-135 cm, usually being shorter and smaller at the top (Doggett,
1988).
Leaf area development establishes the total amount o f radiation intercepted by field crops and
this is an important determinant in assimilation, production and soil water balance. The
importance o f leaf area for grain production has been thoroughly discussed (Wilson and
Eastin, 1982). The result o f agronomic characteristics studied by Brhane and Yilma (1978) has
indicated the presence o f variability in leaf area among sorghum lines across seasons. L eaf
area per plant depends on number o f leaves, rate o f expansion, eventual size o f the plant and
Similarly, the leaves on the main stem may vary in number from 7 to 24 depending on
Variety (Doggett 1988). There are usually 14 to 17 and as many as 30 leaves in well and less
adapted germplasm, respectively. The number o f leaves produced is strongly related to factors
The stem is made o f a series o f alternating nodes and internodes. The stem is slender to very
stout, measuring 0.5 to 5 cm in diameter near the base, becoming narrower at the upper end
(House 1985). Similarly Doggett (1988) has recorded the basal diameter ranging from 5 mm
Sorghum varies in height, which is dependent upon the number o f nodes, which equals the
number o f leaves produced. This is a function o f the maturity length o f the plant (Doggett,
1988). It is also dependent on the internode length and all these factors contributing to height
The panicle in sorghum grows erect at the apex o f the culm, but may be recurved. The wild
and weedy sorghums have a rather loose panicle with spreading branches. Variation in head
width has been reported by several workers (Guiragossion and Melak Ilail 1987; House 1985;
Melakhail and Kao, 1982). Similarly sorghum varies in head length. The variation existing for
this character has been reported by Weibel and Sieglinger (1984). Melakhail and Rao (1982)
have reported head length ranging from 2.5 to 71 cm among sorghum germplasm studied at
ICRISAT Brhane and Yilma (1978) have reported the existence o f variation in head length
Head exertion is the most important characteristic in sorghum production. Sorghum heads that
are not exerted will facilitate the development o f head diseases and insect pests and the quality
12
of the seed will be reduced. On the basis o f world sorghum germplasms Guiragossion and
Melakhail (1987) have reported head exertion ranging from 0 to 55 cm. The distribution o f
sorghum panicle compactness and shape showed clear trends in the three adaptation zones.
The compact panicle types occurred more frequently in the low land than in the intermediate
and high land, while the occurrence o f the loose types generally followed the opposite trend
(Amsalu, 2001).
Grain productivity is usually the primary consideration and genetic characters, environment
and cultural management influence it. The first prerequisite for high yield is a high production
o f total dry matter per unit area, which will depend on the effectiveness o f photosynthesis o f
the crop (Arnon, 1984). The total products o f photosynthesis throughout the life time o f the
crop growing in a given circumstance will depend on the size o f assimilating area, the
efficiency with which it functions and the length o f the period during which it is active. Thus,
characteristics o f the structure and functions o f the organs involved in photosynthesis (Arnon,
1984).
Yield is a complex inherited trait controlled by many genes. Several workers have reported the
existence o f highly significant yield differences among sorghum genotypes (Miller and Yilma,
1984; and Melaku, 1991). With respect to this, Brhane (1979) reported the existence o f more
variability in yield potential in Africa than any other place. This variability is further
confirmed by Reddy et cti, (1990). Similarly the immense contribution o f Ethiopian
Variation in seed size o f 1 to 7.5 mm has been reported (Guiragossion and Melakhail 1987;
ICRISAT, 1990; Melakhail and llao, 1982). The number o f seeds per head is the most
important yield component in case o f field crops. Working with this, Miller and Yilma (1984)
have observed yield increase of a new sorghum hybrid reflecting a significant increase in seed
number with little difference in kernel size. Similarly, Kambal and Webster (1966) indicated
that increased kernel number was primarily responsible for increased yield in sorghum
hybrids.
The apparent increase o f the frequency o f red seed color from low to high and the opposite
trend for w'hite seed color suggests that seed color might have adaptive significance. It seems
that the white grain sorghum lacks certain polyphenolic compounds that serve to protect the
sorghum grain from pre-harvest germination in humid regions in the intermediate and high
land areas, while red and brown colored seeds are rich in polyphenotic compounds (Asante,
1995).
The situation o f sorghum seems to contradict the adaptive significance o f awn in dry areas. It
is likely that the awnless character is favored in sorghum to reduce evapo-transpiration in dry
low land areas. The need for immediate photosynthetic products might be satisfied by the
14
relatively large number o f glumes on a typical sorghum panicle as compared to a typical spike
which are highly heritable and are not likely to change very much under different
and evaluation o f crop germplasm for morpho-agronomic characters is the first step in the
exploitation o f germplasms (Beuslink and Steiner 1992; Melakhail and Rao 1982; Seyfu,
1993).
opportunity and a challenge for crop germplasms conservationists and plant breeders.
Collection and conservation o f sorghum germplasm was accelerated about four decades ago
because o f the danger caused to the landraces by the release o f new varieties and hybrids
(Prasad Rao & Mengesha 1980). Us adaptation to stress environment such as drought, makes
sorghum in a sense more important than other cereals (Yilma and Abebe, 1987; Yilma, 1991).
Plant genetic resources includes landraces, advanced varieties, wild relatives o f domesticated
plants, wild species, genetic stocks and cloned genes (Chang, 1992). Landraces, also known as
traditional varieties, are cultivated forms o f a crop species, which have evolved over
They are also noted as sources o f useful genes required for further increment and maintenance
o f the productivity o f modern varieties, information about the amount and distribution o f
The local community has accumulated the information as a stock within the plant varieties
selected and already in use. Sometimes this selection may have occurred hundreds or even
thousands o f years ago, but the varieties still retain some residual o f their then- existing
such landraces functions as an important part of the agricultural research and development
process; that is, this stock o f information provides immediately identifiable innovation for use
produced information and the consequent selection and use o f the traits and characteristics that
have aided survivability. In this way, traditional plant varieties (landraces) are transformed in
to the accumulated history o f the information, which nature has generated and that farmers
have observed and used. Eventhough germplasms are major source o f crop improvement
Agriculturalists must also continue to supply new forms o f resistance to pests with modern
o f those pests. Genetic resource has value as potential solution concepts to these fundamental
important for use in crop improvement, but perhaps due to limited technical and financial
capacity, the natural variability has not been sufficiently exploited to enhance sorghum
improvement.
At present, ICRISAT is the major repository for the world sorghum germplasms collection
with a total collection o f 26,564 accessions. Among donors, the most important are the
agricultural research station, Sudan, and India (Brown, 1989). Countries like Ethiopia, India,
Sudan and Cameroon have contributed more than half o f the present world collections.
As a single gene or few major genes control most o f the desired traits, it is, thus, obvious that
growing uniform cultivars over vast areas is potentially dangerous. These cultivars are
virulent pathogen because o f their narrow genetic base (IBPGR, 1981). A breeder needs
source of genes for resistance to different stresses for better yield and for nutritive qualities
(Hawkes et a!., 1991). This source o f variation is obtained from germplasms. Besides, the role
in improving yield per se, traditional landraces and their wild relatives, through centuries o f
natural and human selection, can be expected to have acquired resistance to specific pests,
17
diseases and environmental stresses, and can therefore be used as source o f resistance in the
breeding programs.
Collection and characterization o f land races and their relatives becomes very important, in the
source o f vulnerability o f land races following the release o f new varieties and hybrids.
Several primitive landraces once abundant in parts o f Africa and Asia are now extinct.
Therefore collection and conservation o f traditional landraces and their wild relatives is o f
Correlation between characters are o f interest to determine whether selection for one trait will
have an effect on another; hence, selection could be practical on highly heritable traits that are
correlated to a more complex and less heritable trait such as yield. The inadequate knowledge
o f interrelationship among various traits and the practice o f unilateral selection for agronomic
traits frequently end up in less than optimum results in plant breeding. Correlations between
plant characters are an aspect that should be kept in mind for better planning o f selection
In many instances, the breeder is interested in the relationship that may exist between or
among characters. To evaluate relationships, correlation analyses are used in which the values
o f two characters are analyzed on a paired basis. This means that the values for both characters
on some individual or plot are compared for relationship. According to Gomez and Gomez
18
(1984), correlation does not imply or assume any cause and effect relationship between
variables. In fact, one variable could influence the other or vise-versa or both o f them could be
influenced by some third variable. Generally, there are two causes o f correlations between
In line with the association o f characters, Lothrop et al. (1985) have discussed that correlated
responses among plant characters are useful for predicting the effects o f selection and for
determining feasibility o f indirect selection for yield. Geremew (1993) has reported that head
weight, seeds per head, head length, head width, and 1 00 0 seed weight had a direct influence
on yield.
Bittinger et a/. (1981), by investigating the association o f characters, have reported that yield
showed highly significant positive phenotypic and genotypic correlation with panicle weight.
Both panicle and kernel weight are major components o f yield (Eckehil et cii, 1977), Several
crops. Eventhough these estimates are helpful in determining the components o f a complex
trait such as yield, they do not provide an exact picture o f the relative importance o f direct and
indirect influence o f each o f the component character towards this trait. This means that
correlation simply measures mutual association without regarding causation (Agdew 2006).
19
Sokal and R ohlf (1981) noted that selection based on only correlation, without taking in to
consideration the interaction between the component traits, will not be possible to identify the
direct and the indirect influence o f traits on yield. Path coefficient analysis is a statistical
method for determining the magnitude and dissection o f multiple effects o f the components on
yield (Belay et a!., 1993). Moreover, it was stated that, the path coefficients are partitioned
into direct and indirect effects, so that the relative contribution o f each component character to
Path coefficient analysis specifies the cause and measures their relative importance. Bhatt
(1973) suggested that after simple correlation analysis, path coefficient analysis should
provide a true picture o f the association between different traits. It provides an effective means
of untangling direct and indirect causes o f association and permits a critical examination o f the
specific forces acting to produce a given correlation and measures the relative importance o f
causal factors.
partitioning the correlation coefficients in to direct effects (unidirectional path way p) and
indirect effects through alternate path ways (px correlation coefficients (r)), (Bhatt 1973). The
author had stressed that path coefficient analysis was useful in that it revealed the true nature
of cause and effect relationship among different characteristics. Yield is a complex trait
relationships among independent characteristics and the degree o f linear relation between
20
manner. Path coefficient analysis separates the direct effect from the indirect effects through
other related characters by partitioning the correlation coefficient. Path analysis is used when
we want to determine the amount o f direct and indirect effects o f the casual component on the
(entries or environments) into classes based on the characteristics measured prior to the
analysis. This technique initially was developed and used in the area o f taxonomy for several
decades and eventually introduced to the breeding areas in early 7 0 ’s. Elements within the
same group or cluster are relatively homogeneous and elements between clusters arc relatively
heterogeneous (Welsh, 1981). Cluster analysis is also used to group genotypes into
The genotypes are grouped into a number of clusters, D~ being treated as a square o f
generalized distances. The criterion used in clustering is that any two genotypes/ varieties
belonging to the same cluster show, at least on the average, smaller D~ value than those
belonging to two different clusters (Bhatt, 1970). In other worlds, if varieties v\ and v2 are
j / 2
close together and v 3 is distant from the two as shown by their generalized distance (I) = "vD ),
then vi and V2 form a cluster. Previous studies indicated that the same landraces are known by
21
different vernaculars and different landraces by the same vernacular. Hence clustering was
undertaken to classify the identical phenotype into similar groups based on their color and
vegetative measurement.
22
The experiment was conducted at Pawe Agricultural Research Center (PARC) in Benshangul
Gumuz National Regional State, during (he 2005 cropping season. PARC is located at about
580 km north-west o f Addis Ababa at 3 6°25 ’E longitude, 11 ° 12’N latitude and at an altitude
o f 1150 meters above sea level (masl). The area is characterized by hot humid conditions with
mean maximum and minimum temperatures o f 32 °C and 16 °C, respectively. The annual
rainfall ranges from 1500-1800 mm with five and half months long rainy season. The amount
of rainfall in May to mid October is higher than half o f the potential evapotranspiration, and
this period constitutes the growing season. During the months o f July to September the total
rainfall is higher than the full potential evapotranspiration. The total rainfall during the
The soil type is l laplic Altisol, very deep (> 150 cm) and clay in texture. The pH o f the soil
ranges from 5.5 to 6.9 and subsurface soils have higher pH values than surface soils. The
organic carbon ( 2 . 8 to 0 .2 %) and total nitrogen (0.19 to 0 . 0 2 %) content o f the soil decrease
with soil depth. The cation exchange capacity ranges from 20 to 51 Cmolc Kg ' 1 (Abayneh,
2003).
Ninety two sorghum landraces (Table 2), collected from Metekel Zone o f Benshangul Gumuz
and eight standard checks were included in the study. The accessions were collected in 2 00 1
and were maintained at Melkasa Agricultural Research Center. All collections were
maintained by selling five representative heads in each line. Seeds harvested from bagged
Checks
The eight check varieties included in the study are released commercial cultivars
recommended for high and intermediate altitude zones in the country. Early maturing
commercial varieties were deliberately excluded due to discrepancy in maturity dates and
1. Birmash, Baje and 1S9302. These varieties were released for intermediate altitude.
2. Other checks such as chiro, Al-70, ETS-639, E T S -1 176 and Muyera-1 were included just
The accessions were evaluated in 10 x 10 simple lattice design with two replications. The plot
size was 5 m long two rows with a spacing o f 0.75m between rows 0.15m between plants (a
plot area o f 7.5 m2). The spacing between blocks was 1.5m. During planting the seeds were
drilled in rows and at about 2 0 days alter planting thinned to 15 cm distance between plants.
lOOkg/ha DAP and 50 kg/ha Urea were applied at planting and knee height, respectively.
1. Days to em ergence- the number o f days from sowing to 50% emergence o f the plants.
2. Days to flowering- the number o f days from planting to when 50% o f the plants in plot
3. Days to maturity- the number o f days from planting to the date on which seeds on the
4. Yield per plot (gm) - weight o f grain yield taken from the two rows.
5. Head com pactness - scored by visual observations (1-3) scale and were described as loose,
6. Head shape- scored by visual observation (1-3 scale). The type o f head shapes are:
7. Thousand seed weight - this was estimated based on weight of 250 seeds in grams drawn
8. Grain color - was scored based on visual observation (1-3 scale) with white scored as ‘ 1 \
9. Glume color- scored based on visual observation from the plot by considering six types o f
glume color, white (1), yellow (2), brown (3), red (4), purple (5) and gray ( 6 ).
10. Glume cover - scored by visual observation o f the grain on the intact plants from the plot:
11. Number of seeds per head - was calculated from the 1000-seed weight and single head
12. Lodging- assessed by visual observation (1-9 scale) l=free o f lodging, 5= 50% lodged
and 9= 1 0 0 % lodged.
13. Disease and insect pests - common disease and insect pests o f the area like grain mold
and stalk borer were scored using 1-9 scale (1= non infected, 9= highly infected).
The data were collected from 5 plants randomly sampled from each plot.
1. Leaf width (cm) - width of the third leaf from the top measured at its widest part.
2 . L eaf length (cm) - the distance from the collar to the leaf tip o f the third leaf from the top.
3. Number of leaves per plant - leaves were counted from the base to tlag leaf.
4. Single leaf area (cm 2) - was calculated using the formula K x L x W. where I< is the
“adjustment factor” 0 . 747, L is length and W is the width (Stickler et cil., 1961).
5. Leaf area per plant (cm 2) - was calculated by multiplying single leaf area by the number
6. Stalk diam eter (cm) - the maximum measurement was obtained by rotating the mid point
o f the internodes immediately above ground between the jaw s o f a pair o f calipers
7. Internode length (cm) - the distance from the most top node to the next node below.
8. Plant height (cm) - the distance from the base o f the stalk at ground level to the tip o f the
head.
9. Panicle exertion (cm) - the distance from the end o f the Hag leaf sheath to the base o f the
panicle.
10. Head width (cm) -th e diameter o f the head at its widest part.
11. Head length (cm) - the measurement from the base o f the panicle to the tip o f the panicle.
12. Head weight (g) - the mean weight o f the five heads randomly taken from a plot.
13. Yield per plant (g) - the average weight o f grain harvested from five random plants in a
plot.
The frequency distribution graph was used to show the observed variation between qualitative
traits o f the studied genotypes. For example the number o f genotypes with white seeds were
The total variability present in the studied genotypes for each trait was estimated following the
standard procedures o f analysis o f variance for simple lattice design and RCBD ANOVA
(Gomeze and Gomez 1984; Rangaswamy, 1995) using SAS computer package (SAS, 2 0 0 1 ).
Since the relative efficiency o f simple lattice design over randomized complete block design
(RCBD) was low (Appendix 2), computation o f variance components that are used for the
complete block design analysis o f variance was used to drive variance components as
Total rg -1
MSr = mean square of replication. MSg = mean square of genotypes. MSe = mean square of error
RCBD ANOVA was computed using the following model.
Yy = (a + fj +gi + ejj
ih
i> the effect of j replication
The variance components were estimated from the expected mean square using the random
model where the genotypes were considered as shown in Table 2 . The mean squares were
equated to their expectations for the estimation o f variance components. Based on the
Variability was estimated using range, standard error, phenotypic and genotypic variances and
phenotypic and genotypic coefficient o f variation. The phenotypic and genotypic coefficients
o f variation were calculated according to the method suggested by Burton (1953) as:
0 X 100
pcv = ( Y... )
<rlg
X 100
GCV = I Y...
IIcritability in broad sense (hj}2): was calculated according to Allard and hansch (1964) as:
h n2 ^ 2o x 100
Expeclcd genetic advance (GA): was estimated using the formula of Johnson el a /., (1955)
as:
GA <Jlo x k cr _ h2 k cr
Where, cr and cr 2p are defined as above, k is the selection differential.
Covariance analysis followed the same fashion as that o f analysis o f variance, and the mean
cross products were equated with their expectations to solve for the covariance component.
M SCP Expected
Replication r -1 MSCPrxy
df= degrees of freedom. r= number of replications. g= number of genotypes. MSCPrxy = mean sum of cross
product o f replication for trails x and y. MSCPgxy= mean sum o f cross product o f genohpe for traits x and v.
MSCPexv= mean sum of cross product of environment for trait x and y. cr -exy = environment covariance
between iraits x and y. cr -pxy =genotypic co\ ariance of traits \ and y.
Phenotypic correlation, the observable correlation between two variables, which includes both
genotypic and environmental components between two variables, was estimated using the
g" pxy
rpxy = J(o'-px)(cr:py)
cr2gxy
rgxy = v V V K f f V )
Where rpxv is phenotypic correlation coefficient and rgxy is genotypic correlation coefficient
between characters x and y; ^"pxy and & 2frxy are phenotypic covariance and genotypic
Phenotypic ( cr 2pxy) and genotypic ( cr 2gNy) covariance was computed from the table o f
The coefficient o f correlations at phenotypic level were tested for their significances with
table for simple correlation coefficient using g-2 df as suggested by Gomez and Gomez (1984)
IpxXgll
t V 1-r, 2
The calculated Y value was compared with the Y tabulated value at g-2 degree o f freedom.
The correlation coefficient at genotypic level was tested with the following formula forwarded
by Robertson (1959);
lO - r g x t f /
SErgxy = ' Z 2lfxlfy
The calculated t value for each genotypic correlation was tested against tabulated t at (g-2)
degrees o f freedom.
Path analysis followed the correlation analysis. The use o f path analysis requires a cause and
effect situation among the variables. Path coefficient analysis was calculated using formula
suggested by Dewey and Lu (1959) to assess direct and indirect effects o f different variables
r ij = P ij + X r ikpkj
Where r,, is mutual association between the independent traits (i) and dependent variable (j) as
measured by the correlation coefficient, p,j is component of direct effects o f the independent
trait (i) on the dependent variable (j); and Vi'ikPkj is the summation o f components o f indirect
effect o f a given independent trait i on the dependent variable j via all other independent traits
k.
The residual effect (U) was calculated using the formula (Dewey and LU, 1959) as:
U= v 1 - R~ , where R 2 = X rikpkj
Where, U= the residual (unexplained variation o f the dependent variable that is not accounted
In this study, grain yield was considered as the dependent trait and all other traits were taken
as independent traits.
M ahalanobis's generalized distance (D“) statistics was used for assessing the divergence
between genotypes based on 18 traits measured. The generalized distance between any two
Where D “ij = is the distance between any two groups i and j. x 1 anc^ X J are
vector mean o f the traits for the i"’ and j lh groups respectively, and S' 1 = the inverse o f
Group discriminant analysis is used to classify genotypes into one o f the groups based on
future observations. Alemayehu (2003) first introduced its statistical procedure as a statistical
He denoted the linear discriminant function as: L=biXi + 1^2X 2+------------ +bpXp
Where, b l, b 2------ bp are coefficients o f the function which provide maximum discrimination
Xi, X 2 and Xp are the variables from which measurements are taken.
37
The seed colors and head compactness were considered as grouping variables and the
germplasm accessions were classified into either o f seed colors and head compactness type
based on the multiple traits measurements using the SPPS version 10.0 computer program.
The data was standardized using SYSTAT version 8.0 (SPSS, 1998) before discriminant
analysis.
38
Variability was observed in all six traits except for head shape.
The proportion o f genotypes in the white, red and brown grain was 76.5%, 15.5% and 8 %,
respectively (Fig 1). This seems to be the result o f conscious artificial selection that favored
the white colored genotypes and discriminated brown and red ones. Amsalu and Endeshaw
(1998) reported that white and brown seeds were the most frequent grain color types in
sorghum accessions collected from the major sorghum growing areas in the country. The
observed frequencies o f the different color categories in the current study could be
associated with the utilization and disease tolerance aspect o f the crop. Sorghum is the
staple crop in the collection area where white colored grain types make better quality injera
and porridge than the red and brown colored sorghums. Sorghums other than the white
grained types are mainly used for making Telia, a local home made alcoholic drink.
Besides, the white seeded sorghums fetch better market price than the other two sorghum
types and thus it is not surprising that the white seeded types cover large land area than the
red and brown sorghum types. Dogget (1982) similarly indicated that white colored
sorghums are known for their good food quality despite their susceptibility to grain mold.
The white grain sorghum lacks certain polyphenolic compounds that serve to protect the
sorghum grain from pre-harvest germination in humid regions in the intermediate and high
39
land areas, while red and brown colored seeds are rich in polyphenotic compounds (Asante,
1995).
90 -i
80 i
70 1
60 ■
0>
c 50 i
CD
Z3
cr
CD1_____
40 :
Li-
30 ;
10 ;
i
0 1
white brown red
Grain color
Figure 1. Frequency distribution of grain color for 100 genotypes
Most o f the genotypes (92.5%) in the current study were awnless while 7.5% o f them had
awns (Fig .2). The current finding is in partial agreement with previous findings indicating
the frequent occurrence o f aweless sorghums in the lowlands (Amsalu and Endeshaw,
1998). They authors compared sorghum accessions collected from the highlands,
intermediate altitude and lowlands and reported that the presence o f awns increased as one
moves from the lowlands to the highlands. In contrast to the case in small cereals, awn
might have lost its adaptive significance in sorghum as it was reported to be absent in most
40
o f the sorghum genotypes that were collected both in the warm and dry lowlands and the
humid highlands, as was reported by (Amsalu and Endeshaw 1998). In this study on
sorghum collected from Metekel Zone, a zone dominated by lowland areas but where there
exists extended wet growing season, awns seem to play little or no role.
Awn in sorghum might play a significant role in reducing evapotranspiration and that it is
likely that the awnless character is favored in sorghum to reduce evapo-transpiration in dry
low land areas Amsalu and Endeshaw, 1998. In the current study, however, there is no
evidence that would support the suggested role o f awn in reducing evapotranspiration. The
collection area in the current study is wet and warm lowland that represents the north
western lowlands o f Ethiopia where the annual rainfall is 1500 mm and above and where
moisture stress cannot be considered as a serious problem. The role o f awns in reducing
evapotranspiration would not be evident. Nevertheless, Amsalu and Endeshaw (1998) gave
an explanation regarding the absence o f awns in the lowlands as compared to the high and
mid altitude areas o f the country. The more prevalence o f certain foliar diseases in the crop
in the intermediate and highland than in the lowland areas and associated loss o f
100 -
90
80
70
| 60
CD
=3 50
cr
30
20
4.1.3 Head com pactness and head shape of the sorghum genotypes
All the Metekel collections in the current study were characterized by straight heads.
However, few o f the materials that were included as standard checks, were o f the goose
necked types. In the current study, the compact headed sorghum types represent a relatively
small percentage o f the genotypes collected (39%) as compared to the loose head types that
make up 61% o f the genotypes (32% loose and 29% very loose) As shown in Fig 3. The
reason for the observed high percentage o f loose headed materials than the compact headed
materials seems that there was targeted selection o f materials for grain mold resistance.
Grain mold is a major problem in Metekel zone where the relative humidity and rainfall are
high during the main growing season. Compact head types make favorable conditions for
grain mold development. Stemler el a/. (1977) and Prasada Rao and Mengesha (1981) gave
supporting explanation that the open panicle of sorghum is an adaptive trait which
42
facilitates quick drying o f the panicle in areas o f high rainfall and humidity, thereby
Amsalu and Endeshaw (1998) reported similar observation where loose panicle types with
drooping branches occur abundantly in relatively cool and wet regions o f Ethiopia such as
40
35
30 -
25 -
20
15 i
10
5 H
Head c o m p a c tn e s s
100 -
60
H a If c u r v e d S tra i g h t
Head shape
Sixty five percent o f the accessions had grains that are half covered with the glumes, 5% had
uncovered grains while 30% had fully covered grains (Fig 5). Selection seems to have favored
grains either half-covered or uncovered with the glumes. This seems to be an adaptive feature
that facilitates quick drying that minimizes grain mould. Amsalu (2000) observed that the
Collections that had 25% glume covered seeds were the most frequent followed by 50% and
75% in collections from Gamogofa, Gondar, Sidamo and Wello. Glume covers o f 100 % were
the least frequent. However, the reveres were true in the collection form Wellega.
Distribution o f glume color followed seed distribution about 50% o f the accession had white
glumes (Fig 6 ). A gray and red glumes constituted 15% each while brown glumes were
observed in only 4% o f the accessions. Amsalu (2000) has similarly observed the frequent
60
50 -
“ 40
a>
d
cr
.?30
20 -
10
Glum cover
Figure 5. Frequency distribution o f glume covers for 100 genotypes
50
45
40
35 H
O 30
c
0)
3 25 -j
cr
CD
t 20 1
15
10
Glum color
Analysis o f variance indicated that there were highly significant differences (PcO.Ol)
among the genotypes for all traits, days to 50% flowering (DTP), days to 95% maturity
(DTM), leaf width (LW), leaf length (LI.), leaf number (LN), leaf area (LA), plant height
(PH), internode length (INL), Panicle exertion, stalk diameter (STD), stalk borer (STB),
lodging (LOG), head width (HW), head length (HL), head weight (HW), Grain yield/plant
(YPP) and yield kg/ha (Y Kll) (Table 4) indicating the presence o f genetic variability for
the traits studied. Similarly, previous studies on collections from other regions indicate
significant variation for many o f these traits like number o f seeds/head, days to 50%
flowering, days to 95% maturity, leaf width, leaf length, leaf area, plant height and
Since the efficiency o f lattice ANOVA was not high (Appendix 1), we have used RCBD
E ff 101.9 100 100 100.5 100 131.2 101.6 107.6 101.5 100
Table 4. continued
Source of M ean square
V ariation _________________________________________________________________________
Df STB LODG CM HL nvv HWT TSWT NSH VPP YKH
Replication 1 9.68 2.44 0.98 9.768 87.06 83.54 25.92 3.785.28 1.245 32233.10
Genotype 99 1.97** 3.33** 1.76**: 66.29** 8.45** 203.20** 28.79** 274.21 1.26** 1 16.67** 1349769.70**
Error 99 0.44 1.26 0.51 6.9 1.26 53.95 3.49 19191.48 14.93 17158.10
C'V ‘X, 42.14 88.37 40.20 1.3.31 16.89 23.02 11.21 17.64 22.09 15.17
R2 0.74 0.69 0.73 0.84 0.75 0.76 0.81 0.90 0.8.3 0.96
Eff. 113.7 100 100.9 100 109.3 101 100 101 100 100.6
**= Significant al 1%. E ff- efficiency of latlicc ANOVA over RCBD ANOVA% c v - Coefficient of variation R~= Efficiency of the model
DTF=davs to 50% flowering. DTM=days to 95% maturity, LW =leaf width. LL=leaf length. LA=leaf area. LN ~leaf number. PH=plant height, INL=internode
length. PEX=Panicle exertion. STD=stalk diameter. STB=stalk borer. LOG=lodging%. GM=grain mold. HL=head length. HW=head width. HWT=head
weight. TSW =thousand seed weight. NSH=Number of seeds/head. YPP= yield/plant. YKH=Yield kg/h
48
Variability present in the germplasm was estimated from the range o f values for phenotypic
and genotypic coefficients o f variation, heritability and genetic advance o f each character.
A wide range o f values in morpho agronomic traits has been observed in the studied sorghum
germplasm (Table 5). The genotypes had broad range o f maturity period. The early maturing
genotypes reached physiological maturity in 140 days while the late types took 178 days to
mature. More than 90% o f genotypes took more than 160 days to mature. This is because
most genotypes were collected from long growing season area in the sub region. Amsalu
(2000) reported that days to flowering the collections he worked with ranged from 60.58-
(Welo) which suggested that variation in maturity period for sorghum is generally wide and
is perhaps the result o f the difference in agro ecological zones where the crop is grown.
The studied genotypes showed variability in their leaf characters such as leaf width, leaf
length and leaf number and therefore leaf area showed variability among genotypes. The
variation for each leaf character (leaf width, leaf length, leaf number) ranged from
49
6.2 to 10.2 cm for leaf width, 65.6 to 120.8 cm for leaf length, and 8 to 17 for leaf number.
According to Amsalu (2000) mature sorghum leaves may reach a width o f 6.5 to 13.46 cm at
the widest point which is similar to what was observed in the current study. In a related study
by Geremew (1993) leaf length was reported to range from 45.22-126.37 cm and usually
50
shorter and smaller at the top. Similarly, the leaves on the main stem may vary in number
The variability in plant height among genotypes was high and ranged between 150 and 536
cm. The average height recorded was 416 cm, which is very tall. A variability in plant height
o f Ethiopian sorghum from 72 to 615 cm has been reported (Brhane and Yilma, 1978). Even
though the stalk diameter for most o f the genotypes was generally smaller, genotypes were
found to be resistant to lodging. This could be the adaptation o f the genotypes to the area.
There was also remarkable variability in grain mould resistance among the genotypes. The
experimental area is characterized by high rainfall and high temperature. This high moisture
and warm temperature creates favorable conditions for the development o f grain mould. The
variability observed for this trait could be either due to the difference in maturity period and
panicle architecture observed among the genotypes or due to inherent difference in resistance
to the disease. Prasada Rao and Mengesha (1981) have reported that the open panicle is an
adaptive trait, which facilitates quick drying o f the panicle in areas o f high rainfall and
humidity, thereby minimizing grain weathering due to fungal diseases such as grain mould.
Similarly variation in head length ranged from 10 to 44.2 cm which is again within the range
was also noted to range from 0 to 26.4 cm. The range in the international collections was 0 to
Mean grain yield o f the accession was 1663.17 kg/ha with the variation ranging between
25.09-4080.44 kg/ha. Genotype 2001 Pw coll # 059 was the highest vielder o f all. Twenty
four landraces significantly outyielded the standard check variety IS 9302, which gave the
best vielder (2200 kg/ha) among the checks. Out o f these twenty four, eighteen genotypes
gave more than 2500 kg/ha. These include 2001 PW coll # 008, 017, 059, 062, 045, 047, 032,
051, 023, 050, 092, 083, 067, 029, 090, 078, 043, and 039. One o f the eighteen accessions,
2001 PW coll # 92, is in pipeline for release. In general, the standard checks performed
poorly with the yield were low yielders and their yield ranging only between 19.33 and 2200
kg/ha. This is perhaps due to poor adaptation o f the varieties to the area and incidence o f
grain mould and straiga. This indicates that better varieties than currently existing can be
developed for the area using local gerplasm collection as breeding materials.
The presence o f genotypes that outyielded the standard checks is an indication for the
possibility o f developing high yielding varieties from the available materials for Pawe and
similar areas. Therefore, the existence o f wider agro-morphological diversity among the
sorghum collections implies the potential to improve the crop and the need to conserve these
resources.
Heritability estimates are important to indicate the genetic gain that may be achieved through
broad sense heritability (h2), genetic advance in original units and as percent o f the mean
(GA %) for the present study are shown in Table 6. Across the 16 characters, the phenotypic
52
and genotypic coefficients of variation ranged from 5.64-81.13 and 5.62-77.22, respectively.
PCV and GCV values o f roughly more than 20% are considered to be high, values lees than
10% as low and values in between as medium (Deshmukh et . a/., 1986). The lowest PCV and
GCV were obtained for days to maturity while the highest PCV and GCV values were
obtained for panicle exertion (81.13 and 77.2), respectively. For most o f the characters
studied, phenotypic coefficient o f variance was slightly higher than the corresponding
effect on the traits. On the other hand, the relative narrow gap between the corresponding
PCV and GCV values for all characters indicate the low influence o f the environment.
Negash (2003) also reported low values o f genotypic and phenotypic coefficient of variation
for days to flowering, days to maturity and leaf number/plant. He also reported PCV values
(77 %), plant height (78.5%), days to maturity (84.3%), leaf no per plant (74.8%), number o f
Table 6. Means, variance components, PCV, GCV, h2, GA and GA% in the sorghum genotypes for 20 traits of sorghum
genotypes
•>
No. T raits M ean ± SE a 2,, PC V % GCV% h2 GA GA %
1 Days lo flowering (DF) 116.21 ±0.17 89.78 2.37 92.15 8.21 8.15 0.97 0.18 0.15
2 Days lo maturity (DM) 174.72 ± 0.00 96.46 0.79 97.25 5.64 5.62 0.99 0.20 0.11
3 Leaf width (LW) (cm) 8.24 ± 0.44 0.22 0.21 0.43 7.96 5.69 0.51 0.34 4.12
i
4 L Leaf length (LL) (cm) 103.09 ±2.30 89.00 29.10 1 IS .10 10.46 9.15 0.75 0.48 0.46
5 Leaf area (LA) (e n r ) 610.35+572.53 7295.18 2448.36 9743.54 16.17 13.99 0.75 152.25 24.94
6 Leaf number (LN) 14.66 ± 0.41 1.91 0.81 2.72 14.25 9.46 0.70 0.48 3.31
7 Plain height (PH) (cm) 416.03 ± 0.00 5314.72 .362.56 5677.28 18.1 1 17.52 0.94 0.85 0.20
8 Imcmodc length (INL) (cm) 35.20 ± 1.54 31.60 4.62 36.22 17.09 15.96 0.87 10.82 30.74
9 Panicle Exertion (PEX) (cm) 9.69 ± 0.00 56.00 5.81 61.81 81.13 77.22 0.90 0.78 8.05
10 Stalk diameter (STD) (cm) 1.68 ± 0 .1 0 0.04 0.02 0.06 14.58 11.90 0.66 0.43 25.60
11 Lodging (LOG) % 1.40 ± 0.79 0.91 1.50 2.42 112.07 68.92 0.37 1.22 87.31
12 Head width (HW) (cm) 10.25 ± 1.26 2.72 1.51 4.23 20.06 16.09 0.64 2.73 26.63
13 Head length (HL) (cm) 28.67 ± 1.86 26.66 6.49 33.15 20.08 18.00 0.80 0.64 2.23
14 Head weight (HWT) (g) 34.27 ±5.19 70.68 30.92 101.60 29.41 24.53 0.69 14.45 42.17
15 lOOOsecd weight (TSW ) (g) 23.74 ± 1.32 10.87 3.52 14.39 15.98 13.88 0.75 5.90 24.85
16 Number of seed / head (NSH) 1000.97197.96 12.2092.80 15012..81 137105.61 36.99 34.91 0.89 679.25 67.86
17 Grain mold (GM) (1-9 scale) 2,25 ± 0.26 0.60 0.55 1.15 53.77 38.75 0.51 1.29 57.54
18 Stalk borer (STB) (1-9 scale) 2.82 ± 0 .4 7 0.13 1.51 1.82 50.38 20.87 0.17 0.50 17.82
19 Yield /plant (YPP) (g) 21.65 ±2.73 46.97 1 1.37 58.34 35.28 3 1.66 0.80 12.67 58.52
20 Yield Kg /ha (YKH) 1663.17 ± 92.62 63.3721.62 41163.35 674884.97 49.39 47.86 0.94 880.33 52.93
SE=standard e rro r. a 2g= Genotypic variance. a 2c = Environnemental variance. ct2p= Phenotypic variance. PC V % -phenotypic coefficient of variation.
GCV%= Genotypic cocfficieni of variation, lr = heritability. GA = Gcnctic advance. GA % ^Genetic advance as percent of mean
54
Swamp and Chaugale (1962) reported low heritability for grain yield while other authors
(Abu-El-Gasim and Kambal, 1975) reported higher value (93.3%). Medium heritability was
observed for stalk diameter (66%), head width (64%), head weight (69%) and leaf width
(51%). In general heritability was high for all quantitive charters studied suggesting that
selection for the traits would be effective. But it should be noted that this is broad sense
heritability and hence is not absolute indicator o f selection efficiency. According to Singh
(1999), if heritability o f a character is very high, say 80% or more, selection for that
character is easy, but the masking effect of the environment is high on traits with low
Estimates o f expected genetic advance ranged from 0.18 days for days to flowering to 880
kg/ha for grain vield/ha (Table 6). That is, the resultant population obtained after crossing the
best 5% o f the materials will produce a new population whose days to flowering is earlier
than the older population by 0.18 days , and whose yield kg/ha is better than the older
the superiority o f the new population. Low predicted response to selection was observed for
days to flowering (0.18), days to maturity (0.20), leaf width (0.34), leaf length (0.48 cm), leaf
number (0.48), plant height (0.85 cm) head exertion (0.78 cm), head length (0.64 cm), and,
1000 seed weight (5.9 g). I Iigh values o f genetic advance were observed for leaf area (152.25
cm2), number o f seeds/head (679.25) and grain yield kg/ha (880.33 kg). Negash (2003)
reported high value o f genetic advance for plant height (82.2 cm), leaf area (91.3 cm2) and
kernel number/panicle (373.1). Genetic advance less than 10%) was reported by Negash
(2003) for leaf number/plant, panicle length, panicle width, head weight, 100 kernel weight
ranged from 0.11% for days to maturity to 87.3% for lodging and number o f seeds/head.
Genetic advance as percent o f the mean was high for head weight (42.17%), number o f seed
per head (86%), yield per plant (50%), and yield kg/ha (52.93%). Estimates o f genetic
advance greater than 10% but less than 40% were observed for leaf area (24.94%), internode
length (30.74%), head width (26.63%), stalk diameter (25.60%) and thousand seed weight
(24.85%). Genetic advance less than 10% were observed for leaf width, leaf length, days to
flowering, days to maturity, plant height, panicle exertion, leaf number and head length.
Negash (1997) reported intermediate to higher genetic advance as percent o f mean for plant
height (43.3%), kernel number/panicle (65.5%). head weight (40.5%), grain yield per plant
(45.8%) and 100-kernel weight (56%) for highland sorghum o f eastern Ethiopia.
In this study, intermediate to high PCV and GCV values were observed for most of the
traits. Low PCV and GCV values were obtained for days to flowering, days to maturity and
leaf width. O f all the characters evaluated, head weight, grain vield/plant, number o f
seeds/head and grain yield kg/ha appear to combine relatively high values o f GCV, hr and
GA (% o f the mean), making them most important characters, that can easily be improved by
selection. According to Panse (1957), higher heritability coupled with high genetic advance
as percent o f the mean suggests that the traits are controlled by additive gene action.
Therefore, this study indicated that the environment had less influence on these traits and
relatively rapid progress can be made for these traits through plant breeding.
56
The estimates o f genotypic correlation coefficients among 20 traits are shown in Table 7.
Generally, the genotypic correlation coefficients were higher than their respective phenotypic
correlation coefficient which is in agreement with the findings o f Johnson et cil. (1955),
Weber and Morthy (1952), Negash (1997) and Negash (2003). This was explained to be the
result o f the masking and/or modifying effect of environment on the phenotypic association
among traits.
On the basis o f correlation alone (Table 7) head weight, thousand seed weight and number o f
seeds/head had strong and positive correlation with grain yield per plant at both genotypic
and phenotypic level. This shows that selection for, head weight, and number o f seeds/ha can
result in a high yielding variety. Negash (2003) and Geremew (1993) reported that grain
yield per plant manifested positive and strong association with yield/plot, head weight, and
hundred-kernel weight and kernel number. Geremew (J993) indicated positive and
significant association o f grain vield/plant with all yield components except head length at
Melkasa.
The association o f stalk borer attack and lodging with grain yield/plant was negative at both
genotypic and phenotypic level. This indicates that growing o f sorghum in an area where
there is high prevalence o f wind and stalk borer results low yield.
57
A negative genotypic correlation between two traits indicates that increase in one trait would
result in the reduction o f the other; increase or decrease o f both traits simultaneously would
be difficult.
Information on association between grain yield and its components is important for selection
o f the component that was most related to yield. Head weight, number o f seeds/head and
thousand seeds weight were more closely associated both genotypically and phenotypically
with grain yield/plant. Therefore, according to this study selection for higher values o f these
Days to flowering was positively and significantly correlated with days to maturity, leaf
number, and plant height at genotypic and phenotypic level (Table 7). Negash (2003)
reported similar result for the association between days to flowering and plant height and
days to maturity; this indicates that genotypes, which took longer time to flower, will also
take longer time to mature, are taller and tend to have more number o f leaves. Tall genotypes
seem to take longer time to flower and mature and hence do not complete the normal grain
filling period under the erratic rain fall conditions, specially during rain fall shortage at late
maturity in an area like Mankush (around pawe). Therefore, grain filling period seems
shorter than what it could have been under longer seasons. Tall genotypes also take more
time to flower and mature and produce proportionally high dry matter than reproductive sink
Plant height was positively and strongly correlated with internode length and head length at
both genotypic and phenotypic level. This result indicates that taller genotypes have longer
The association o i'leaf number with days to flowering and days to maturity was positive and
significant at both genotypic and phenotypic level, while the association o f lea number with
leaf area, plant height, stalk diameter, head width, grain mold and leaf length was positive
and significant at genotypic level; but leaf number had negative association with panicle
exertion. This result indicates that plants with more number o f leaves have larger stalk
diameter, panicle head and are more susceptible to grain mold disease. When there is more
number o f leaves/plant, the possibility o f creating high humidity within the plant canopy will
Stalk borer infestation is negatively correlated with days to flowering, days to maturity, plant
height, internode length, head length, number o f seeds/head and yield/plant. From the
positive correlation o f stalk borer and stalk diameter, it seems that the female moth prefers
laying eggs on genotypes with thicker stalks. This provides more food for the emerging
larvae.
In general, correlation between thousand seeds weight and number o f seeds/head was almost
zero, which means that it is possible to identify genotypes that have many big seeds/head.
Visual selections for genotypes with bigger heads possessing many big seeds would lead to
the identification o f genotypes that give higher yields. At both genotypic and phenotypic
level, leaf number and plant height have weak negative correlation with grain yield/plant and
59
grain yield kg/ha. Leaf width is positively correlated with grain yield. The same trend is
observed for leaf length at the genotypic and phenotypic level. Therefore, to develop high
yielding varieties the breeder should look for shorter genotypes with fewer but longer and
wider haves.
60
Table 7 Estimate o f genotypic (above diagonal) and phenotypic (below diagonal) correlation coefficient among 21 traits in
100 sorghum genotypes grown at Pawe in 2005.
C h a ra cte r DTF DTM LW LL LN LA PH I NL PEX STD STB LOG HL HW HWT TSW NSH GM YPP YK
DTF 0.918 0.107 0.389 0634 0.297 0.637 -0 032 -0 0 2 9 0 266* -0.37 0.162 0.051 0.118 0 001 -0.03 0.101 0 734” 0.047 -0.037
DTM 0.904” 0 173 0.419 0.706 0.341 0.632 -0 088 -0.078 0 282* -0.336 003 -0.035 0 134 -0.065 -0.074 0.085 0.131 0 018 -0.039
LW 0.076 0 13 0.731 0.409** 0.888 -0.311 -0.7 -0 782 0 .6 7 3 " 0.345** -0.226” -0.774 0 761” 0.519 0.435* 0.217 0.846** 0.223 0 044
LL 0.34” 0.37** 0.485** 0 57 0 963 0.001 -0.22 -0.669 0.647* 0 378 -0.341 -0.21 0.588 0.412 0 666 0.027 0 702 0.277 0.154
LN 0.529” 0.593** 0.35** 0 472* 0.542 0.468 -0.412 -0.506 0.619” 0.104** 0.296” -0.397 0.602 0.062 0.158 -0.068 0.535** -0.081 -0 198
LA 0.258** 0.3” 0.81” 0.904” 0.484” -0.131 -0 43 -0.763 0.706 0.401 -0.321 -0.445 0692 0.488 0.627 0.107 0.814 0.274 0.126
PH 0 614” 0.61** -0 237* 0.001 0.396” -0.119 0.452 0.413 -0.186 -0.492 0.054 0.532 -0.33 -0.197 -0.304 0 06 -0.337 -0.053 0.038
1 NL -0.029 -0 0 8 -0.534* * -0.161 -0.343-* -0.368” 0.418** 0 667 -0.682 -0 192 -0.353 0.988 -0.875 -0.179 0.01 0.062 -0 625 0.115 0.186
PEX -0.024 -0.078 -0.539* * -0.557” -0.411* * -0.633” 0.407” 0.611” -0.777” -0.383 -0.167 0.735 -0.903 -0.323 -0.441 *’' 0.054 -0.802 -0.133 0 047
STD 0.218 0.235* 0.564” 0.498” 0.603” 0.606” -0 159 -0.536” -0.623” 0.45” 0.191” -0.773” 0.713” 0.096 0.294” -0.16 0.586” -0.139*’* -0.353
STB -0.24 -0.2 3 2 ' 0.17 0 .224' 0.008 0 .238' -0.3 2 7 ” -0.169 -0 291 ” 0.214* - 0.017 -0.135 0.113 -0.137 0.177 -0.452 0 .292” -0.352 -0.235
LOg 0.114 0.03 *0.135 -0.187 0.139 -0.19 0.31” -0.264* -0.139 0.124 -0.096” -0.247* 0 057 -0.33 -0.262 -0.442 0.033 -0.542 -0.465
HL 0.043 -0 0 2 7 '0.444* * -0.171 -0.307* * -0.326” 0.444” 0.836” 0.634” -0 507** -0.163 -0.337” -0 6 1 5 ” -0.158 -0.084 0.1 -0.483 0.167 0.253
HW 0 096 0.109 0.526” 0.475” 0.433” 0.57*' -0.26** -0 .6 5 3 " -0.699” 0.564” 0 288” 0.031 -0.956” 0.568 0.414 0.15 0.883 0.181 0.325
HWT -0.013 -0.05 0.347” 0.321** 0.055 0.386** -0.137 -0.088 -0.242' 0.096 -0.15 -0 .5 1 4 " -0.114 0.463** 0.451 0.812 0.295 0.815 0.528
cn
TSW -0.018 -0 056 0.27* 0.12 0.471” -0.219* -0.006 -0.368” 0.196 0.144 -0.194 -0 049 0.321” 0.395” -0.005 0.157 0.447 0.275
o
o
NSH 0 08 0.078 0 168 0.033 -0.06 0.105 0.056 0.062 0.041 -0 107 -0.315” -0.296** 0.078 0.142 0.739” -0.015 -0.06 0.854 0.581
GM 0.078 0.116 044” 0.493** 0.347“ 0.544” -0.268” 1 -0.474” -0.634*’ 0.365” 0.427” 0.09 -0.374” 0.481” 0.151 0.272* -0.026 0.048 -0.021
YPP 0.039 0.016 0.195 0.235* -0.042 0.255* -0.038 0.124 -0.097 -0.071 -0.259* -0.345” 0.116 0.166 0.767” 0.386” 0 804” 0.009 0.765
YKH -0.039 -0.039 0.012 0.129 -0.158 0.096 0.056 0.184 0.078 -0.286** -0.178 -0.338** 0.218 0.038 0.482” 0.256* 0 549** -0.039 0.706**
4.5 P a th A n a ly s is
Grain yield per plant is a resultant trait o f other component traits. Hence, path coefficient
analysis was carried out at genotypic and phenotypic levels considering grain yield per plant
as the dependent trait and other traits as the causal factors. Seven traits which are a subset o f
all other traits best explained the correlation with grain yield per plant. When all the 19 traits
were used the residual was 48%, while with these 7 traits the residual was only 6% (94% was
explained).
The genotypic direct (bold) and indirect effects o f 7 traits on grain yield per plant are shown in
Table 8. The direct effects o f number o f seeds/head (2.076), thousand seeds weight (0.676),
head width (1.879) and internodc length (1.181) were positive, l'he other traits like stalk borer,
head weight and leaf area had negative direct effects on grain vield/plant. Negash (2003)
found that traits such as thousand seed weight, head weight, number of seeds/head, panicle
width and leaf area had positive direct effect on yield per plant. Contrary to this, Negash
(1997) and Shahane and Borikar (1982) reported maximum positive direct contribution o f
head weight to grain vield/plant. Number o f seeds/head exerted high positive direct effect
(2.076) on grain yield/plant and exerted positive indirect effects through head width. Similar
result was reported by Geremew (1993), where number o f seeds/head was the most highly
Table 8. Genoypic direct effect (bold) and indirect effects of 8 traits on grain yield per plant.
NSH=Number of seeds/head, TSW =Thousand seeds weight, SB= Stalk borer attack. HWT= Head weight. HW= Head width,
1NL= Intemode length. LA= Leaf a re a .. rg= Genotypic correlation coefficient
63
Thousand seeds weight exerted intermediate direct effect on yield per plant. The indirect
effects o f this trait were positive through head width. Negash (2003), Singh and Baghel (1977)
reported high direct effects o f hundred-kernel weight and kernel number/head on grain
yield/plant in grain sorghum. This result shows that number o f seeds/head can be used as the
best indicator o f grain yield/plant for indirect plant selection for higher yield since its both
direct effect and genetic correlation with grain yield/plant were high and positive.
Although the genotypic correlations o f head weight and leaf area with grain yield per plant
were positive, the direct effects of these traits on grain yield/plant were negative. The positive
correlation was due to the indirect effects exerted on grain yield/plant through number o f
seeds/head, thousand seeds weight and head width. According to Singh and Chaudhary
(1977), whenever a character has positive association and high positive indirect effects but
negative direct effect on the economic trait like grain yield, emphasis should be given to the
indirect effects. Selection o f heavy heads with bigger diameter that contain many big seeds
The correlation coefficient o f head width with grain yield/plant was positive and the direct
effect was positive. The positive genetic correlation resulted not only from the high and
positive direct effect but also from high and positive indirect effects o f the trait through
number o f seeds/head and thousand seed weight. Therefore, for higher yield indirect selection
Internode length exerted high positive direct effect, but low positive association with grain
yield/plant. Its indirect effect through number o f seeds/head was positive. Stalk borer had also
low negative direct effect and low negative correlation with grain yield. Genotypes tolerant to
stalk borer should be selected. The indirect effect o f number o f seeds/head, thousand seed
weight, and head width on grain yield through head weight are negative pointing to the
necessity o f selecting wider heads with many big seeds. Selection o f only heavy heads with
out considering other traits will produce genotypes with undesired characters which may
The phenotypic direct and indirect effects o f yield related traits on grain yield/plant are
presented in Table 9. Number o f seeds/head and thousand seed weight exerted positive high
direct effect on grain yield/plant. Negash (2003) reported that kernel number/panicle exerted
maximum positive direct effect on grain yield//plant followed by hundred-kernel weight and
head weight. Kernel number/panicle and head weight also correlated strongly and positively
Indirect selection for grain yield per plant through these traits would be effective. The causes
o f high positive phenotypic correlations o f grain yield/plant with head weight were due to the
high and positive direct effect o f head weight on yield per plant and its positive indirect effect
The high correlation coefficient at both genotypic and phenotypic level and the high positive
direct effect o f number o f seeds/head and thousand seed weight and their positive direct effect
65
on grain yield/plant via head weight makes these two traits the best indirect selection criteria
for high grain yield. These traits also manifested high heritability and genetic advance as
percent o f the mean. The importance o f path analysis here is that, although at the genotypic
level the direct effect o f head weight on grain yield was negative its indirect effect through
NSH=Number o f seeds/head, TSW=Thousand seed weight, STB= Stalk borer attack, HWT= Head weight,
HW= Head diameter, IN L - Internode length, LA= Leaf area, rp= Phenotypic correlation coefficient
67
4.6 C lu s te r A n alysis
Eighteen quantitative traits were used as input for cluster analysis. Ward's method which
minimizes within cluster variance was used in this study with the SPSS computer software
(SPSS. 1998). This method appeared to give the most satisfactory clustering result with most
populations included in clusters o f similar size (Smeath and Sokal, 1973). The clustering
obtained using W ard’s method grouped the original 100 genotypes in to ten clusters as shown
in Table 10 and Figure 7. Clusters contained from 1 to 23 members. Clusters means of the
Sorghum landraces from different woredas of Metekel were grouped in the same cluster and
landraces from similar woredas were distributed in different clusters. . No geographic pattern
because the collection area is small and farmers exchange seeds. Therefore, sorghum
landraces collection expedition should be launched and searching for traits o f interest would
Appendices
Dsst an ce
Genotypes
70
Cluster 1, II, III, V, VIII, IX, X contain late maturing genotypes having 115-121 days to
flowering and 171-178 days to maturity. Accessions in these clusters are tall (401- 512 cm)
Cluster IV is intermediate in maturity and is composed o f six checks (ETS 1176, AL70. ETS
639, Chiro, Muyra-1 and Muyra-2), released for the highland zones. Genotypes under this
cluster are tall (422.08cm). They are characterized by the fewest number o f seeds per head
(286), while the lowest value after this is that o f cluster 10 (380).
Cluster V represented accessions that are characterized by shorter height (160.50 cm) and
internode length (25 cm), which made them more important for future use as breeding
materials. Because most o f the tested Metekel sorghum landraces are very tall (above 4
Cluster VI and VII are composed o f early flowering and maturing accessions: 74-112 days to
flowering and 122-133 days to maturity. Cluster VI is composed o f 3 released Varieties (Baji,
IS9302, Birmash) and they were standard checks, which are short seasoned lowland materials
used as standard checks in this experiment. They have the lowest stalk diameter (1.36). Their
thousand seed weight and yield per plant is among the lowest.
Cluster VII consisted o f only one genotype (2001 pw coll # 092). This genotype is an outlier
in its characters and it is in the pipeline for release. In the past four years o f yield trial, this
71
genotype had highly significant difference in resistance to grain mold and striga infestation
with other genotypes. It is characterized by relatively shorter time to flowering (75), and
maturity (122) with a height o f 233.70cm, but had longer internodes (46.70cm), panicle
exertion (21.70cm) and head length (35.50cm). Head weight (66.55g), thousand seed weight
(34.00g,) number o f seeds/head (1321) and yield/plant (40g) o f this genotype were higher.
This genotype could be considered as important source for most o f the traits o f interest.
SPH 1 152.00 793.00 1,278.00 286.00 819.00 799.00 1,321.00 1,266.00 945.00 380.00
YPP 27.27 19.53 25.36 5.13 17.58 16.10 40.00 23.94 21.21 6.24
YKH 2750.29 1591.79 1776.58 188.92 736.66 1542.45 2741.33 1905.22 2102.00 623.42
DTF=days lo 50% flowering, DTM=days to 95% maturity. LW =Ieaf w idth. LL ~leaf length, LA=lcaf area, LN=leaf number. PH=plant height. INL=inter node
length. PEX=Panicle exertion. STD=stalk diameter. HL=head length. HW=head width. HWT=head weight, TSW =thousand seed weight. NSH=Number of
seeds/head, YPP= yield/plant, YKH=Yield kg/ha
73
Inter cluster distance (D2) was computed and the results are presented in Table 12. Distance
between clusters 1 and II was minimum (D2 =7.67) followed by that o f clusters VIII and IX
(13.53), 1 and VI (15.06) and II and III (19.19). The maximum distance was found between
As maximum Variations in the subsequent generations is expected from crosses that involve
parents from the clusters characterized by maximum inter-class distances, the crossing o f
2001 pw coll # 092 from cluster VII with those from clusters VIII and IX is expected to
produce desirable recombinants. Cluster VII which consisted only “2001 PW coll # 092”
accession is expected to produce segregates with moderate to high variations if they will be
crossed with parents selected from cluster I, 11 and 111. Since the inter cluster distances
between cluster VI and I, 11 and III were fairly large, hybridization o f parents selected from
cluster VI with parents from clusters I, II and III can produce progenies with desirable
variations.
On the other hand, crossing between cluster 1 and II; II and III; VIII and IX could not
produce desirable recombinants since the inter-cluster distances between these groups were
very small indicating their closeness and similarity o f their genetic make up. Distances
between clusters I and III; I and IV; I and VIII; 1 and IX; II and IV, VIII, IX; III and IV; IV
and VIII, IX; VIII and X; IX and X were also observed to be small (Table 12). Thus
crossings that involve parents from these groups may not produce progenies with desirable
variations.
74
Therefore, crossing distant clusters like 2001 PW coll # 92 cluster VII which is high yielding,
early maturing, with relatively short height and resistant to grain mold and striga, with parents
selected from cluster I (2 0 0 1PW coll # 8, 23, 32, 39, 47 and 50), II (2001 PW coll # 029, 043,
062 and 51) and 111 (2001 PW coll # 017, 045 and 042) which are late maturing, relatively
high yielding and tall could be good to reduce the hight, increase yield and improve other
important characters like grain mold and striga resistance. These are varietal types suitable for
Fable 12. Inter I)" value of’ the 10 clusters of sorghum genotypes
IX 44.36
X
75
The 100 genotypes were regrouped in to 3 types o f seed color (white, brown and red) and head
compactness (loose, very loose and compact) groups, based on visual observation. The
objective here was to see whether the classification made based on difference in seed color
and head compactness before quantitative data collection was correct or not after data o f 16
In this study, taking the three types o f seed colors and head compactness as grouping
variables, the mean values o f each o f the 16 traits for each genotype were subjected to SPSS
The results o f the classification based on seed color and head compactness are given in Tables
13 and 16, respectively. Using the mean values o f the 16 traits, 75 white-seeded genotypes
were classified into: 64 to their original white, 3 entered the brown and 8 entered the red
group. The result indicates that 85% of the original white color seeded genotypes were
correctly classified, 4% entered into group o f brown and 10.7% entered into group o f red
The eight brown-seeded genotypes were classified: seven to their original brown, one entered
the white and none entered the red. The result indicates that 87.5% o f the original brown color
seeded genotype is correctly classified, 12.5% entered the group o f white. The 15 red seeded
genotypes were classified into: 1 1 to their original red, 2 entered the white and 2 entered into
brown. The result indicated that 73.3% o f the original red color genotypes is correctly
76
classified, 13.3% entered into group o f brown and 13.3% entered into group o f white land
races.
When the results o f all groups are considered together about 83.7% o f the total population o f
sorghum landraces studied was with minimum overlap, correctly classified into their
respective group during group formation, which was done during seed preparation before
planting.
For classification o f seed color more contribution had been seen from traits like days to
maturity, days to flowering, head length and stalk diameter (Table 17). Mean o f the three seed
color groups are presented in Table 14. The white colored genotypes were late maturing, tall
and relatively high yielding. Red seeded group is early maturing and low yielding.
77
Table 14. Group means of 21 traits of white, brown and red colored
sorghum genotypes studied.
Grain color
Trait White Brown Red
Days to flowering 116.96 106.87 100.6
Days to Maturity 176.15 157.00 163.4
Leaf width (cm) 8.47 7.52 8.36
Leaf length (cm) 103.23 81.87 92.16
Leaf Number 14.30 13.22 12.62
Leal area (cm ) 9413.80 6193.99 7493.82
Plant Height (cm) 371.63 353.62 311.00
Internode length (cm) 31.61 30.80 32.40
Exertion (cm) 4.70 8.37 6.12
Stalk diameter (cm) 1.75 1.68 1.66
Head width (cm) 1 1.24 9.87 9.40
Head length (cm) 24.36 22.94 22.86
Head weight (g) 35.86 17.80 26.12
Lodging (%) 1.19 5.50 1 89
Leaf diseases 1.00 1.62 1.80
Grain mold 2 2.87 2.00 2.00
Stalk borrer 3 2.69 2.75 3.60
Thousand seed weight (g) 23.91 19.50 21.60
Number o f Seeds per head 1015.99 472.26 662.22
Yeild per plant (g) 22.33 9.16 14.49
Yield (K/ha) 1626.26 760.38 898.13
leaf diseases scored on a scale of 1 to 9 where 1 = free of disease and 9
=most of the leaves infected
Grain mold infected seeds scored on a scale of 1 to 9: where. 1 = mold free
and 9 com pletely molded seeds
Stalk borer damage on a scale of 1 to 9; 1 = free of borer damage and 9 =
most damaged
78
Table 15. Variables ordered by absolute size of correlation within function for grain
color classification of sorghum.
F u n c tio n
1 2
.5460 - 195
Days to maturity
5450 -.467
Days to flowering
.3080 014
Head length
-2 7 0 0 081
Stalk diameter
.2610 .072
Number of seeds/head
226(*) - 037
Panicle exertion
.2230 187
Leaf length
.164(*) 086
Internode length
-.0900 -.030
Head width
.165 .3630
Head weight
.315 -.3310
Plant height
- 013 .294(*)
Thousand seed weight
.028 .257O
Leaf width
167 .2140
Yield/plant
005 -,160(*)
Leaf number
085 .1170
Leaf area
Using the mean values o f the 16 traits, out o f the 27 loose head sorghum genotypes 15 entered
their original loose head, 7 went into very loose head and 5 entered the compact head
genotype. The result indicated that 55.6% o f the original loose head genotypes are correctly
classified, 25.9% entered in to very loose head, 18.5% entered the compact head genotype.
Thirty of the 41 very loose head sorghum genotypes were classified to their original very loose
head, 10 to loose head and one to compact head. The result indicated that 73.2% o f the
original very loose-headed genotypes are correctly classified, 24.4% entered into group o f
The 32 compact head genotypes were classified in 25 to their original compact head, 7 to
loose head and none to very loose headed genotypes. The result indicated that 78.1% o f the
original compact headed genotypes are correctly classified, 21.9% entered in to group of loose
headed land races. When the results o f all groups are considered, about 70.0% o f the total
population o f sorghum land races studied was correctly classified into their respective group
during group formation, which was done during seed preparation before planting. Therefore,
discriminant analysis efficiently separated the groups with some over lap based on head
compactness.
80
Loose 15 7 5 27
Original Count Very loose 10 30 1 41
Compact 7 0 25 32
Loose 55.6 25.9 18.5 100
% Very loose 24.4 73.2 2.4 100
Compact 21.9 0 78.1 100
For classification o f head compactness more contribution had been seen from traits like head
exertion, plant height, internode length and head length ( Table 18). According to the
functions and group mean value; the compact head genotypes had shorter height, head
exertion, internode length, were early maturing and relatively low yielding; while loose
headed genotypes were tall, had lower head exertion, internode length and were late maturing.
Higher grain mold disease was observed on the compact headed genotypes. This result
indicates that genotypes with compact head should not be selected for areas like Pawe, which
have, high humidity and high temperature, which facilitate grain mold.
Therefore, it can be concluded that the different colored and head compactness type sorghum
land races are not only different in seed color and head compactness but they also differ in
most quantitative traits. Hence, selection for traits o f interest on group bases is advantageous
instead o f accessing the whole gene pool o f sorghum land races. This also indicates that some
81
quantitative traits are linked with some qualitative traits. Qualitative traits which are easy to
Table 17. Group means of 21 traits ofloose , very loose and compact headed
sorghum genotypes studied.
Head compactness
Traits Loose Very loose Compact
Days to flowering 116.76 118.21 113.14 ± 017
Days to Maturity 174,80 176.96 171.16 ± 0.00
Leaf width (cm) 8.42 8.08 8.33 ± o.44
Leaf length (cm) 101.68 96.41 98.79 ± 2 .3 0
Leaf Number 14.24 14.30 13.90 ±0.41
Leaf area (cm2) 9258.13 8445.10 871 1.33 ±572.53
Plant Height (cm) 421.95 455.94 359.91 ± 0.00
Internode length (cm) 35.61 37.74 31.63 ± 1.54
Exertion (cm) 8.88 13.60 5.38 ± 0 .0 0
Stalk diameter (cm) 1.73 1.61 1.72 ± 0 .1 0
Head width (cm) 10.52 9.67 10.78 ± 1.26
Head length (cm) 27.65 29.13 23.95 ± 1.86
Head weight (g) 37.52 33.56 32.01 ±5.19
Lodging (%) 1.25 1.13 1.84 ± 0 .7 9
Gram mold ~ 1,98 1.52 2.62 ± 0 .2 6
Stalk b o r r e r 3 2.63 2.49 2.84 ± 0 .4 7
Function
1 2
Panicle exertion .699(*) -.319
Plant height .5990 .233
Internode length .4580 .224
Head length .404(*) .131
Head weight -.3420 .291
Days to flowering ,2040 .108
Days to maturity .1750 .059
Leaf length -.216 .6970
Leaf area -.215 .6060
Head weight -.014 .567(*)
Yield/plant .067 .5120
Tousand seed weight -.122 .4920
Leaf widith -.259 .4160
Stalk diameterl -.261
CO
CO
o
*
Leaf number -.053 .2750
Number of seeds/head .132 .271 (*)
G Group Centroid
□ 1= loose
* 2 = Ve r y loose
■ 3 = Compact
Ninety-two land race collections and eight checks (standard) were included in the present
study. The experiment was arranged in a 10 x 10 simple lattice design. Data was collected on
There was variation in the qualitative traits o f the landraces under study. The white, brown and
red grain color genotypes constituted 76.5%, 8% and 15.5%, respectively. Selection favoring
the white color grain land races has been practiced by the local people.
Genotypes with awned glume were only 7.5% while the awnless glume genotypes were
92.5%). The distribution o f loose, very loose and compact headed genotypes was 32%, 29%
and 39%, respectively. All Metekel collections had straight heads, 3% checks had goose head.
It seems that the selection favoring the awnless genotypes with straight heads has been
operating. Despite the importance o f head compactness, farmers do not seem to have paid
great attention to this trait. Mild selection for loose head types (61%) has been operating.
among the genotypes for all traits. Sixteen genotypes gave grain yield better than the best
standard check (IS 9302) indicating the possibility o f identifying superior genotype to be
released as a variety or to be used in the breeding program. These include 2001 pw coll # 059,
062, 045, 047, 032, 051, 023, 050, 092, 083, 067, 029, 090, 078, 043, and 039.
86
The tested sorghum genotypes showed a wide range o f maturity time (113-180 days), leaf
width (6.2-10.3), leaf length (67.6-120.8), leaf number (8-17.6), plant height (150-536 cm),
head length (10-44.2), panicle exertion (0-26.4), and grain yield (19.3-4590 kg/ha).
The phenotypic and genotypic coefficient o f variation values o f the 16 characters ranged from
5.64-81.13 and 5.62-77.22, respectively. Low PCV and GCV (<10%) were obtained for days
to flowering and maturity, and leaf width. Leaf length had low GCV. Highest PCV and GCV
value (81.13 and 77.2%, respectively) was obtained for panicle excretion and yield kg/ha.
In this study heritability for all traits except lodging (37%) and stalk borer attack (17%) was
(>50%). Greater than 20% genetic advance was obtained for all traits except days to flowering
(0.15%), days to maturity (0.11%), leaf width, length and number (4.12%, 0.46% and 3.31%,
respectively), plant height (0.2%), panicle exertion (8.05%), head length (2.23%), and stalk
High heritability and high genetic advance as percent o f the mean were observed for leaf area,
internode length, stalk diameter, head width, head weight, thousand seed weight, number o f
seeds per head, grain yield per plant and grain yield in kg/ha indicating that these traits were
governed by additive genetic action. In such traits, relatively rapid progress can be achieved
through selection.
Genotypic and phenotypic correlations among 20 traits and grain yield/plant were generally
low for most o f the traits showing these traits cannot be used for indirect selection for yield.
87
However, grain yield/plant showed strong positive correlation with head weight (0.815 and
0.767), number o f seeds/head (0.854 and 0.767) and thousand seed weight (0.447 and 0.386)
at genotypic and phenotypic levels, respectively. Path analysis has revealed that number o f
seeds/head and thousand seeds weight had strongest direct effect on grain yield. The direct
genetic effect o f head weight on grain yield was negative. The high positive genetic
correlation o f head weight with grain yield per plant was expressed through the indirect effect
of this trait on yield per plant through number o f seeds per head and thousand seed weight.
These three traits also had high heritability and genetic advance as percent o f the mean and
can therefore be used for indirect selection for yield per plant.
Cluster analysis based on the 20 traits assessed has grouped the genotypes into 10 distinct
clusters. Mehlanobis distance (D“) varied for different pairs o f clusters. The highest heterosis
and the highest possibility o f transgressive segregants is expected from the crosses o f elite
genotypes from distant clusters. The only accession that belongs to cluster VII is 2001 pw coll
# 092. This landrace has many desirable traits including grain mould and striga resistance. It
can be crossed with the highest yielding genotypes from cluster I, II and IV.
Discriminating genotypes into three distinct seed color and head compactness groups based on
16 quantitative traits revealed that classification using quantitative traits confirmed the
previous qualitative classes for most genotypes. The result showed that 87.5% o f the original
brown, 73.3% o f the original red and 85% o f the original white seeded genotypes were
correctly classified, while 55.6% o f the original loose head, 73.2% o f the original very loose
88
and 78.1% o f the original compact headed genotypes were correctly classified to their
respective classes after considering quantitative traits for classification. Their mean value
indicated that the white seeded and loose headed genotypes are late maturing, are high
yielding and tall, while the red seeded and compact headed genotypes are early maturing, low
yielding and short, and more susceptible to grain mould. Therefore, this study indicated that
different seed color and head compactness groups are different in many quantitative traits.
This may indicate linkage between qualitative and quantitative traits. The qualitative traits,
therefore, can be used as markers for indirect selection for specific quantitative traits including
grain yield.
89
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APPENDIX
Appendix 1. Genotype means of 18 traits
Appendix 1. continued
Appendix 1. continued
2001 pw coll #004 17.2 1.93 1.7 8.9 32.3 26.7 26 881.55 2 14.8 578.00
2001 pw coll #005 16 2 1.58 1 11.05 24.5 32.7 26 873.21 3 22.5 1799.33
2001 pw coll #006 3.6 1.78 1 11.1 27.4 32 32 734.38 2 20.3 1878.00
2001 pw co ll #007 10.2 1.94 1 11 30.9 43.4 28 1010.71 2 28.3 1609.33
2001 pw coll #008 1.8 1.74 1.7 12 23.6 33.6 28 1081.93 2 28.3 2553.33
2001 pw coll #009 7.6 1.75 1 10.85 29.9 41.8 28 923.96 2 26.2 1644.00
2001 pw co ll #010 3.9 1.59 1 10.9 25 43 5 26 1207.74 2.5 31.3 1925.33
2001 pwcoll #011 6.6 1.84 1 14.02 25 48 24 1256.25 1 14.15 1120.67
Baji 10.3 1.21 1 5 35 23.9 32.82 20 1015.00 3 18.3 1096.67
2001 pwcoll # 0 1 2 8.7 1.89 1 10.2 26.1 32.1 20 864.25 3 14.6 592.67
2001 pwcoll #013 7.6 2.23 0.75 10.8 25.3 34.7 32 542.19 4 17.35 456.67
2001 pwcoll #014 5.3 2.29 1 13.3 23.7 39.9 24.5 987.00 2 21.8 1171.33
2001 pwcoll #015 5.6 1.94 1 12.3 17.7 50 6 34 1161.00 1 28.8 2058.67
2001 pwcoll #016 5.1 2.04 1 11 30 5 43.1 28.5 1082.50 1 30.65 2062.00
2001 p w c o l# 0 1 7 2.5 2.02 0.75 12.4 22.8 40.6 24 1245.83 2 31.3 2512 67
2001 pwcoll #018 8.1 2.13 1 11.45 28.9 48.7 22 1404.00 1 25.75 1307.33
2001 pwcoll #019 3.2 1.93 0.75 118 23 7 38 6 24 1123.57 1 26.9 1873.33
2001 p w coll #020 0.7 1.7 1.7 10.27 19.8 28.1 24 607.83 2 12.19 265.33
2001 pw coll #021 3.9 2.06 1 11.5 18.8 33.6 24 979.17 2 21.1 997.33
2001 pw coll #022 3.7 1.61 1 11.4 22.8 46 28 1046.43 1 29.3 1644.00
2001 pw coll #023 44 1.66 0.75 13 28.4 43.6 22 1485.00 3 27.9 2788.00
ETS-1176 1 1.97 0.75 13.65 15.5 23.8 26 203.14 2 4.1 225.33
2001 pw coll #024 2.3 1.72 1 11.2 21.8 27 4 24 862.17 3 19.7 1403.33
2001 p w co ll #025 3.6 1.87 1 10.1 26.8 40.2 26 1058.33 3 24.1 1800.00
2001 pw coll #026 1.5 1.76 1 9.9 28.8 28.8 28 828.36 3 22.6 2189.33
2001 pw coll #027 4.2 2.01 1 10.88 26.2 36.9 24 875.00 3 21 1362.00
2001 pw coll #028 5 1.71 1.7 9.8 28.5 26.9 24 1334.00 3 26.25 1308.00
2001 pwcoll #029 6 1.54 1.7 10.58 24 25.5 24 806.50 4 20.75 2716.67
2001 pwcoll #030 3.5 1.62 1 15.2 15 1 59.4 18 1763.75 4 22.9 1678.67
AL70 10.3 1.59 0.75 12.3 20.7 24.5 20 118.75 3 2.25 20.00
2001 pwcoll #031 4.1 1.71 1 104 23.45 37.1 24 972.00 3 22.5 2043.33
2001 pwcoll #032 8.3 1.68 1 10.1 28.2 42.7 28 1246 50 1 32.1 2996.67
2001 pwcoll #033 4.9 1.77 0.75 11.4 28.6 33.1 24 706.43 4 25.1 1756.67
2001 pwcoll #034 2.8 1.91 4.05 7.9 30.6 30.7 24 841.67 3 20.2 1005.33
2001 pwcoll #035 6.9 1.73 1.7 8.4 26.8 34.9 24 893.75 3 21.45 1378.00
2001 pwcoll #036 4 2.16 0.75 10.75 25.9 29.3 24 1366.43 1 30.5 2091.33
101
Appendix 1. continued
2001 pwcoll #037 2.8 1.68 1 9.4 21.3 28.2 26 662.50 1 17.3 1285.33
2001 pwcoll #038 9.2 1.75 1 10.85 30.8 33.1 20 910 00 3 16.2 1558.00
2001 pwcoll #039 3.1 1.72 1 10.7 24.9 41 24 1112.50 3 26.7 2628.00
2001 pwcoll #040 5 1.51 0.75 11.13 27.1 36.2 24 1002.25 3 21.65 2059.33
ETS-639 0 2.05 4.75 12.5 12.4 17 16 306.67 2 3.8 96.00
2001 pwcoll #041 2.2 1.76 1 11.9 24.2 42.2 28 1024.79 3 25.3 1510.67
2001 pwcoll #042 3.9 1.83 1 14.7 28.7 40.3 28 1165.93 3 22.05 1514.67
2001 pwcoll #043 1.6 1.68 0.75 10.6 29.1 30.1 32 707.81 3 22.65 2643.33
2001 pwcoll #044 13.4 1.78 1 96 22 6 33.5 22 1231.50 3 27.2 2452.67
2001 pwcoll #045 3.4 1.68 1 13.54 21 2 41.5 22 1356.67 3 26.05 3144.67
2001 pwcoll #046 1 1.87 1 13.5 24.7 37.2 26 1000.67 2 23.15 2470.00
2001 pwcoll #047 0.4 1.75 1 11.27 29.1 42.8 30 1073 00 3 34.5 3092.00
2001 pwcoll #048 4.4 2.09 4.05 13.37 23.3 43.6 20 1357.29 3 27.05 1106.67
2001 pwcoll #049 4.2 1.53 1 11 25.6 39.3 26 1333.50 2 29.7 1411.33
Birmash 10.7 1.39 1 9.8 25.6 24.5 24 583.33 3 14 1281.33
2001 pwcoll #050 1.6 1.6 1 11.15 27.3 35.9 22 1083.33 3 23.7 2772.00
2001 pwcoll #051 7.6 1 76 1 11.2 27.4 40.6 26 774.40 3 20.1 3018.67
2001 pwcoll #052 ' 6.1 2.09 1j 13.7 19.4 60.3 24 1508.33 2 26.2 1784.00
2001 pwcoll #053 5.1 1.81 1 10.8 18 44.8 18 1697.50 2 29.3 1628.00
2001 pwcoll #054 8 1.7 1 11.42 26.7 37.7 18 1355.00 3 25.6 1820.00
2001 pwcoll #055 3.2 1.9 1 11.1 26.7 52.7 22 1775.83 3 32.3 2081.33
2001 pwcoll #056 1.5 1.77 1.7 12.33 26.9 38.5 28 1121.14 3 27.2 1638.67
2001 pwcoll #057 15.3 1.42 1 7.4 31.4 27.1 16 1169.00 1 23.1 1500.67
2001 pwcoll #058 23.7 1.22 1 7.1 31.8 33.9 22 988.33 1 21.65 1526.00
2001 pwcoll #059 22.5 1.61 j 1.7 8 7j 27.9 44.2 20 1587.50 1 31.75 4080.00
2001 pwcoll #060 6.9 1.99 1 10.7 14.2 28.2 24 966.00 1 20.25 944.00
2001 pwcoll #061 14.3 1.75 1 11 18.2 23.3 22 672.50 2 14.9 529.33
IS9302 15.5 1.48 1 6.75 31.15 24 20.5 800.00 2.5 16 2249.34
2001 pwcoll #062 5.3 1.42 1 10.9 23 39.5 28 1201.57 2 30.25 3547.33
2001 pwcoll #063 3.3 1.5 1 10.55 27.1 45 26 975.60 3 25.2 1732.00
2001 pwcoll #064 17 3 1.56 1 6.6 40.9 15.1 23 404.00 2 5.75 774.67
2001 pw coll #065 0 1.42 1 10.35 25 .2 ^ 43.6 26 1043.45 3 26.9 1104.00
2001 pw coll #066 23.3 1.58 0.75 54 38.4 13.9 20 270.00 1 5.4 512.00
2001 pw coll #067 24.4 1.4 1.7 7.9 32.1 19.5 22 614.17 1 13.6 2752.00
2001 pw coll #068 22.7 1.5 1 7.9 30.9 34.1 20 1245.00 1 24.9 1684.00
2001 pw coll #069 22.5 1.61 0.75 6.27 39.6 18.5 16 668.75 1 10.7 859.33
2001 pw coll #070 19.85 1.73 1 8.2 32.3 12.7 18 176.25 1 3.1 374.67
2001 pw coll #071 22.9 1.46 1 8.1 26.6 24.7 18 1253.75 1 21.2 1717.33
2001 pw coll #072 24.5 1.59 1 6.7 31.6 32.6 20 1107.50 1 24.15 1484.67
2001 pw coll #073 22.1 1.37 1.7 7.46 31.1 22.3 20 735.00 1 14.7 2189.33
102
Appendix 1. continued
2001 pw coll #074 24.9 1.48 0.75 8.1 29.2 28.7 20 1130.00 1 22.6 1945.33
2001 pwcoll #075 21.7 1.33 1 8.3 33.6 30.5 22 896.25 1 19.55 2232.67
chiro 5.5 1.72 5 11.25 21.5 13.5 16.5 375.00 3 6 522.52
2001 pwcoll #076 18.1 1.45 1 8.25 31 31.7 26 844.05 1 21.7 1789.33
2001 pwcoll #077 18.3 1.36 1 9.1 29.2 29.9 24 445.83 1 15.7 2288.67
2001 pwcoll #078 21 4 1.45 1 7.7 32.9 34.1 20 1240.00 1 29.8 2648.00
2001 pwcoll #079 21.5 1.29 1 8.7 31.2 43.4 20 2110.00 1 22.2 1916.00
2001 pwcoll #080 20.1 1.35 1 6.6 32 27.4 20 1242.50 1 23.85 1353.33
2001 pwcoll #081 21.2 1.34 1 11.8 33.4 28.3 22 807.50 1 17.9 1527.33
2001 pwcoll #082 16.2 1.25 1 8.17 37 39.1 20 1297.50 1 25.95 1844.67
2001 pwcoll #083 16.5 1.39 0.75 9.1 39.8 40 24 1527.25 1 29.45 2730.67
2001 pw coll #084 14 1.4 1 8.05 32.7 30.4 24 800.00 1 19.2 1885.33
2001 pw coll #085 21.5 1.46 1 8.1 35.3 32.9 24 1069.00 1 21.8 1186.00
2001 pw coll #086 17 9 1.34 1 7.4 40 7 23.1 22 917.50 1 21.65 1008.67
2001 pw coll #090 25.9 1.24 1 9.6 35.1 37 24 1322.14 1 29.9 2692.00
Murya-2 6 1.75 9 11.5 23 16.5 20.5 573.81 2 11.75 250.33
2001 pw coll #092 21.7 1.18 0.75 11.2 35.5 66 55 34 1321.53 1 40 2741.33
GM= grain mold. ML = Head length. HW = Head weight. HWT - Head weight. TSW T = Thousand seed weight. NSPH =
Number of seeds/liead. YKha = Yield kg/ha. DTF=davs to 50% flowering. DTM=days to 95% maturity. L\V=leaf width.
LL=leaf length. LN =leaf number. PH=plant height. INTL=inter node length. PEXE=Panicle exertion. STD=stalk diameter.
Lodging
Appendex 2. Thirteen years mean monthly Rainfall of Pawe in mm.
N o ;; M onth '- 'S |g l9 9 4 •'1 9 9 5 W 6 1996 1399 zm o 2001 20Q2 2003 2004 200$ £006
1 J a nu ary • 0.0 0.0 0.2 0.0 0.0 2.2 0.0 0.0 0.0 0.0 0.0 0.0 9.2
2 F ebru ary M 0.0 0.0 42.5 0.0 0.0 0.0 0.0 0.0 0.0 0.0 0.0 0.0 11.2
3 M arch • j 0.0 35.5 42.5 2.1 9.8 0.0 0.0 0.0 0.0 0.0 I 0.1 18.1 0.0
4 A p ril 13.7 14.8 88.8 2.1 9.6 0.0 6.0 4.9 8.3 1.8 83.3 2.9 18.6
5 M a y -.' 164.7 92.7 206.0 147.4 153.6 180.7 201.5 100.3 10.3 24.8 58.4 43.8 152.7
6 June / :;1 198.2 413.9 370.5 180.4 511.9 280.9 270.0 296.3 344.8 287.2 356.8 176.0 216.6
7 J u ly 290.7 233.3 532.7 330.0 384.8 285.7 195.3 347.4 244.0 402.3 | 416.6 388.4 401.9
8 A u g u s t . ;j 304.6 433.6 272.2 388.3 366.6 359.2 337.9 503.5 355.8 360.2 J 475.3 311.6 | 706.2
9 S eptem ber | 304.8 248.0 144.5 175.4 243.0 223.6 179.8 248.1 212.5 301.9 I 294.7 250.7 263.1
10 I d c t o b e r l l l ! 77.9 91.6 12.3 170.0 146.7 134.6 192.2 167.5 139.7 109.3 | 69.7 153.9 192.3
11 N o v e m b e r j 51.1 0.0 0.0 16.9 5.6 19.2 17.5 0.0 23.3 5.9 15.1 3.2 5.9
12 D ecem ber | 0.0 1.4 0.0 1.4 6.0 4.3 7.0 0.0 0.0 0.0 4.0 0.0 0.0
to ta l 1405.7 1564.8 1712.2 1414.0 1837.6 1490.4 1407.2 1668.0 1338.7 1493.4 1774.0 1348.6 | 1977.7
Biography
The author was born in October 1967 at Belessa woreda, North Gondar. He attended his
primary and secondary school at Arbaya town and Gondar comprehensive secondary
In 1985 he joined Awassa Agricultural College and graduated with diploma in plant
Organization (EARO), he joined the Alemaya University in 1997 and graduated with
bachelor o f science degree in plant science in 2000. After graduation the author again
joined EARO and worked at Pawe Agricultural Research Center until the end o f 2004.
In February 2005, the author joined the School o f Graduate Studies o f Hawassa