ABSTRACT
Maize (Zea mays L.) is an annual plant belonging to
the family (Graminae or Poaceae). It is a major cereal crop in West
Africa, accounting for slightly over 20% of all food crops produced for
domestic production in the sub-region. It is one of the most important cereals
in Ghana, which is cultivated in all the agro-ecological zones. The objectives
of this study were to estimate the general and specific combining ability
effects of the inbred lines, determine the mode of gene action controlling
grain yield and drought tolerance. A study was undertaken to assess the combining
ability of 17 early and 26 intermediate maize inbred lines and one check for
each genotypic group for drought tolerance using line by tester (line x tester)
analyses. This trial was conducted in the screen house of the Department of
Horticulture, KNUST in 2016. A randomized complete block design with three
replications was used in the experiment. Some inbred lines with desirable
general combining ability (GCA) effects for the studied traits were identified
under drought-stress condition. For early maize genotypes inbred lines L1
followed by L4 were best general combiners for number of kernel row per ear,
number of kernels per row, cob weight and grain yield under drought-stress
condition. For intermediate maize genotypes under drought-stress condition, the
line L4 was best general combiner for grain yield, cob weight, number of kernel
rows per ear and ear diameter for their positive and significant GCA effects.
These lines could be selected for their good traits to develop high yielding
hybrids and for further exploitation in a breeding programme. Hybrid
combination, L7 x T2 and L8 x T1 under well-watered condition and L6 x T2 under
drought-stressed condition for intermediate maize genotypes were good specific
combiners for grain yield while, for early maize genotypes, crosses were not
significant for yield under well-watered and drought-stress conditions.
The low ratio of 2gca/ 2sca, in the current study showed
the preponderance of non-additive gene actions for almost all the traits for
early and intermediate maize genotypes. The inbred lines L1 (S6-15-22) and L4
(CML538) for early maize maturity genotypes and L4 (CML502) for intermediate
maize maturity genotypes were identified as best general combiners that can
withstand drought-stress. These lines showed positive and significant GCA
effects for yield and yield-related traits under drought-stress condition. The
cross L6 X T2 was identified as good specific combiners that can withstand
drought-stress for the positive and significant SCA effect for grain yield and
yield-related traits under drought-stress condition.
Positive and significant mid-parent heterosis was observed
under drought-stress condition for early and intermediate maize maturity
genotypes. The crosses L2 X T1 and L3 X T2 observed high mid-parent heterosis
for early and intermediate maturity genotypes, respectively. Generally, the
results of the current study identified crosses with good level of heterosis,
inbred lines with good GCA effects and cross combinations with desirable SCA
effect for the traits studied. The results indicate the possibility of
developing desirable cross combinations through crossing and or recombination
of inbred lines with desirable traits of interest. Hence, the information from
this study could be useful to researchers who would like to develop high
yielding varieties of maize under drought-stress condition.
TABLE OF CONTENTS
ABSTRACT
LIST OF ABBREVIATIONS
CHAPTER ONE
1.0 INTRODUCTION
CHAPTER TWO
2.0 LITTERATURE REVIEW
2.1 Botany and description of
maize
2.2 Importance of maize
2.3 World maize production
2.4 Challenges of drought to
maize production
2.5 Drought stress effects on
maize
2.6 Adaptation of maize to
drought
2.6.1 Strategy to drought
adaptation or tolerance
2.6.2 Drought escape
2.6.3 Drought tolerance
2.7 Inbred lines development
2.8 Concept of line x tester
analysis and combining ability
2.8.1 Line x tester analysis
2.8.2 Combining ability
2.9 Heterosis
CHAPTER THREE
3.0 MATERIALS AND METHODS
3.1 Experimentation site
3.2 Experimental materials
3.3 Design and Experimental
management
3.4 Soil sampling and
analyses
3.5 Planting
3.6 Irrigation schedule
3.7 Fertilizer application
3.8 Statistical analyses
3.8.1 Analysis of variance
3.8.2 Combining ability
analysis
3.8.3 Genetic components
3.8.4 Proportional
contribution of lines, testers, and line by tester interaction to the total
variation
3.8.5 Heterosis
CHAPTER FOUR
4.0 RESULTS
4.1 Soil analysis
4.2 Analyses of Variance
(ANOVA)
4.2.1 Early maturity maize
genotypes
4.2.2 Intermediate maturity
maize genotypes
4.3 Estimates of general
combining ability effects
4.3.1 Early maturity maize
genotypes
4.3.2 Intermediate maturity
maize genotypes
4.4 Specific combining
ability effects
4.4.1 Early maturity maize
genotypes
4.4.2 Intermediate maturity
maize genotypes
4.5 Estimates of genetic
component and proportional contribution to the total variances
4.5.1 Early maturity maize
genotypes
4.5.2 Intermediate maturity
maize genotypes
4.6 Mean performances of
genotypes and heterosis
4.6.2 Intermediate maturity
maize genotypes
CHAPTER FIVE
5.0 DISCUSSION
5.1 Analyses of variance for
early and intermediate maturity maize genotypes
5.2 General combining ability
effect for early
and intermediate maturity
maize genotypes
5.3 Estimates of specific
combining ability for early and intermediate maturity maize genotypes
5.4 Estimates of genetic
component and contributions to the total variances for early and intermediate
maturity maize genotypes
5.5 Mean performances and
heterosis for early and intermediate maturity maize genotypes
CHAPTER SIX
6.0 CONCLUSIONS AND
RECOMMENDATIONS
REFERENCES
CHAPTER ONE
1.0 INTRODUCTION
Maize (Zea mays L.) is an annual
plant belonging to the family Graminae or Poaceae (Sprague and Dudley, 1988).
It is a major cereal crop in West Africa, accounting for slightly over 20% of
all food crops produced for domestic consumption in the sub-region (IITA,
2000). It is cultivated in all the agro-ecological zones of Ghana (Fening et
al., 2011). Worldwide, maize is currently the third most traded cereal, after
wheat and rice, with more than 160 million hectares cultivated every year
(FAOSTAT, 2010). The production was estimated to be 985 million tons for the
2012/2013 season an increase of 9% from 2011/2012 (Brandt, 2013).
According to Badu-Apraku et al.
(2011), in West and Central Africa (WCA), maize is consumed directly and serves
as major staple diet for some 200 million people, providing about 15% of the
total caloric intake of rural and urban consumers, while in developed
countries, it is mainly used as livestock feed (DuPlessis, 2003). Industrially,
maize is used to produce alcohol, starch, pulp, abrasive, and oil in the
pharmaceutics and recently for fuel production (Morris, 2007; Acharya and
Young, 2008).
The demand for maize in developing
countries is expected to be about 504 million tons by 2020 and this is expected
to exceed the demand for both wheat and rice (IFPRI, 2000). To meet this
demand, there is a need for increased maize production in the developing
countries while maintaining the same land resources since population growth and
environmental conditions limit the opportunity for increasing maize area
(Pingali and Pandey, 2001). The need to increase maize production in developing
countries is challenged by a number of constraints including both abiotic and
biotic stresses. Among the major
abiotic stresses limiting tropical maize production are drought and low soil
fertility. Drought is known to cause substantial reduction in the economic
yield of crop plants, a major threat to food security, sustainability of
production systems, and the well-being of people living in drought-prone areas.
It adversely affects the lives of 2.6 billion people (43% of the world
population) that are engaged in agriculture (Saxena et al., 2002). Possibly due
to climate change, drought effects on maize production are generally severe in
the dry Savanna zone of West Africa (Fajemisin et al., 1985). This is because
rainfall in this region is irregular in terms of timing (can start early or
very late in the season), quantity (some times less than 600 mm/annum) and
distribution (could be poorly distributed) (Izge and Dugje, 2011). Most
tropical maize is produced under rain fed conditions, and in area where drought
is considered to be the most important abiotic constraint to production
(CIMMYT, 1999).
Drought at any stage of crop
development affects production, but grain yield losses can be greater if the
drought stress occur at the most drought-sensitive stage of crop growth, such
as flowering and grain filling. Drought stress can reduce yield by 50% when it occurs
at flowering period, by 21% when it happens at the grain filling stage (Denmead
and Shaw, 1960), and by 90% when it strikes from few days before tassels
emergence to the beginning of grain filling (NeSmith and Ritchie, 1992).
Drought would intensify in the
years ahead in response to climate change (Acquaah, 2012), Therefore, the
survival of resource-poor, small scale maize growers in sub Saharan Africa who
cultivate drought-susceptible maize varieties with little or no access to
irrigation facilities has become a great challenge.
According
to FAO (2006) and Derera et al. (2008), additional irrigation could possibly
improve maize production in drought prone areas but in general, most rain fed
farmers are resource poor, smallholders, and have a limited capacity to adopt
high-input technologies (Bänziger and Diallo, 2001; FAO, 2006). A better
approach to help these resource poor subsistence farmers is by using varieties
that tolerate or escape the periodic droughts which befall the region.
One of the most important
conditions for identifying high yielding hybrids is the information about
parents’ genetic structure and their combining ability (Ceyhan, 2003). The
choice of selection and breeding method to be used for genetic improvement of crop
plants therefore, will depend on the magnitude of genetic variability and the
nature of gene action leading the inheritance of desirable traits (Aminu and
Izge, 2013).
Line x tester analysis method
(Kempthorne, 1957) is a tool widely used by plant breeders to generate reliable
information on the general and specific combining ability effects and aids in
selecting desirable parents and crosses. This method has been used in maize
breeding by several workers and continues to be applied in quantitative genetic
studies in maize (Rawlings and Thompson, 1962; Joshi et al., 2002; Sharma et
al., 2004). The effectiveness of this method depends mainly upon the type of
tester used in the evaluation. According to Hallauer (1975), a suitable tester
should be simple in use, provide information that correctly classifies the
relative merit of lines, and increases the genetic gain. Although, it is
difficult to identify testers having all these characteristics, it can help to
provide information to estimate the combining ability and also the type of gene
action involved in the expression of yield and yield related traits.
Therefore,
in the present study, the main objective was to undertake analysis of 17 early
and 26 intermediate maize inbred lines for grain yield and drought tolerance.
The specific objectives were to:
assess the general and specific
combining ability of the parents and hybrids for yield and drought tolerance,
determine the nature of gene action
controlling the traits of yield and drought tolerance of the inbred lines;
identify parents and hybrids that
can withstand drought stress, and
estimate heterosis for yield and
drought stress.
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