This document discusses recurrent selection, which is a breeding method used to improve cross-pollinated crops. It involves selecting single plants based on their phenotypes over multiple generations of selfing and intermating. There are different types of recurrent selection including simple recurrent selection, recurrent selection for general combining ability, and reciprocal recurrent selection. The document also discusses heterosis, inbreeding depression, hybrids, and methods for producing hybrid crops.
Heterosis breeding
Heterosis or hybrid vigour or outbreeding enhancement
Types of heterosis
Genetic basis of heterosis
HYBRIDS
Development of inbreds
Combining ability
Types of hybrids
Single cross hybrid
Double cross hybrid
Triple cross hybrid
Top cross hybrid
The primary distinction between a test cross and a backcross is that a test cross is used to determine the genotype of a phenotypically dominant individual, whereas a backcross is used to recover a dominant genotype from a parent who has an extreme genotype.
The hybrids that are backcrossed are known as 'BC' hybrids. For example, a BC1 hybrid is an F1 hybrid that was crossed with one of its parents or a genetically similar species. The BC2 hybrid is defined as a BC1 hybrid that has been crossed with the same parent or genetically similar species. Other instances include backcrossing in animals.
A system of breeding in which repeated backcrosses are made to transfer a specific character to a well-adapted variety for which the variety is deficient is referred to as backcross breeding
This approach is infrequently utilized in vegetatively propagated crops such as sugarcane and potatoes, and only with slight alterations.
A test cross is a genetic technique for determining an unknown genotype in a dominant person. It is a breeding procedure in which a (known genotype) homozygous recessive individual is paired with an individual of the opposite mating type who has an unknown dominant genotype.
The phenotypic characteristics of the resulting children are investigated, and the genotype of the examined individual is determined appropriately.
If all of the progeny from the test cross are dominant, we may conclude that the genotype of the tested unknown person is homozygous dominant.
If 50% of kids exhibit dominant traits and the remaining 50% exhibit recessive traits, we may conclude that the genotype of the tested unknown individual is heterozygous dominant.
#genetics #backcross #testcross #mendel #crosses #monohybridtestcross #backcrossandtestcross #typesofcross #dihybridtestcross #limitationsofcross #applicationsofcross #mscbotany #botany
Hello, everyone! I am Abhishek Singh, a passionate scholar in the field of genetics and plant breeding. With a profound love for plants and a curiosity about their genetic makeup, I embarked on a journey into the world of science and agriculture. Currently pursuing my studies in genetics and plant breeding, I am dedicated to unraveling the mysteries of plant genetics and contributing to the development of sustainable agricultural practices.
Heterosis, also known as hybrid vigor, refers to the superiority of an F1 hybrid over its parents in terms of traits like yield, vigor, and resistance to diseases. There are two main hypotheses for the genetic basis of heterosis: the dominance hypothesis, which attributes heterosis to the masking of deleterious recessive alleles in hybrids, and the overdominance hypothesis, which posits that heterozygosity at certain gene loci leads to greater vigor. Heterosis can be classified by type, such as individual, maternal, or paternal heterosis, and by origin as either true (eu) heterosis resulting from mutational or balanced genetic combinations, or pseudoheterosis involving only vegetative superiority. Factors like
This document discusses the concept of heterosis, also known as hybrid vigor. It defines heterosis as the superiority of F1 hybrids over their parents in traits like yield, vigor and adaptation. The document then discusses the history of heterosis research and different hypotheses for the genetic basis of heterosis, including dominance, overdominance and epistasis. It also covers types of heterosis estimates and how heterosis is manifested. Factors affecting heterosis and various methods for heterosis breeding in crops are outlined.
This document discusses recurrent selection, which is a breeding method used to improve cross-pollinated crops. It involves selecting single plants based on their phenotypes over multiple generations of selfing and intermating. There are different types of recurrent selection including simple recurrent selection, recurrent selection for general combining ability, and reciprocal recurrent selection. The document also discusses heterosis, inbreeding depression, hybrids, and methods for producing hybrid crops.
Heterosis breeding
Heterosis or hybrid vigour or outbreeding enhancement
Types of heterosis
Genetic basis of heterosis
HYBRIDS
Development of inbreds
Combining ability
Types of hybrids
Single cross hybrid
Double cross hybrid
Triple cross hybrid
Top cross hybrid
The primary distinction between a test cross and a backcross is that a test cross is used to determine the genotype of a phenotypically dominant individual, whereas a backcross is used to recover a dominant genotype from a parent who has an extreme genotype.
The hybrids that are backcrossed are known as 'BC' hybrids. For example, a BC1 hybrid is an F1 hybrid that was crossed with one of its parents or a genetically similar species. The BC2 hybrid is defined as a BC1 hybrid that has been crossed with the same parent or genetically similar species. Other instances include backcrossing in animals.
A system of breeding in which repeated backcrosses are made to transfer a specific character to a well-adapted variety for which the variety is deficient is referred to as backcross breeding
This approach is infrequently utilized in vegetatively propagated crops such as sugarcane and potatoes, and only with slight alterations.
A test cross is a genetic technique for determining an unknown genotype in a dominant person. It is a breeding procedure in which a (known genotype) homozygous recessive individual is paired with an individual of the opposite mating type who has an unknown dominant genotype.
The phenotypic characteristics of the resulting children are investigated, and the genotype of the examined individual is determined appropriately.
If all of the progeny from the test cross are dominant, we may conclude that the genotype of the tested unknown person is homozygous dominant.
If 50% of kids exhibit dominant traits and the remaining 50% exhibit recessive traits, we may conclude that the genotype of the tested unknown individual is heterozygous dominant.
#genetics #backcross #testcross #mendel #crosses #monohybridtestcross #backcrossandtestcross #typesofcross #dihybridtestcross #limitationsofcross #applicationsofcross #mscbotany #botany
Hello, everyone! I am Abhishek Singh, a passionate scholar in the field of genetics and plant breeding. With a profound love for plants and a curiosity about their genetic makeup, I embarked on a journey into the world of science and agriculture. Currently pursuing my studies in genetics and plant breeding, I am dedicated to unraveling the mysteries of plant genetics and contributing to the development of sustainable agricultural practices.
Heterosis, also known as hybrid vigor, refers to the superiority of an F1 hybrid over its parents in terms of traits like yield, vigor, and resistance to diseases. There are two main hypotheses for the genetic basis of heterosis: the dominance hypothesis, which attributes heterosis to the masking of deleterious recessive alleles in hybrids, and the overdominance hypothesis, which posits that heterozygosity at certain gene loci leads to greater vigor. Heterosis can be classified by type, such as individual, maternal, or paternal heterosis, and by origin as either true (eu) heterosis resulting from mutational or balanced genetic combinations, or pseudoheterosis involving only vegetative superiority. Factors like
This document discusses the concept of heterosis, also known as hybrid vigor. It defines heterosis as the superiority of F1 hybrids over their parents in traits like yield, vigor and adaptation. The document then discusses the history of heterosis research and different hypotheses for the genetic basis of heterosis, including dominance, overdominance and epistasis. It also covers types of heterosis estimates and how heterosis is manifested. Factors affecting heterosis and various methods for heterosis breeding in crops are outlined.
This document provides information about genetics and Mendelian inheritance. It begins with an introduction to important figures in the history of genetics like Gregor Mendel. It then discusses the three main theories of inheritance pre-Mendel and the history of genetics including Mendel's experiments and laws of inheritance. The rest of the document details various genetics concepts like linkage, crossing over, aneuploidy and their relationships to chromosomes and inheritance patterns.
The back cross method involves crossing a hybrid plant with one of its parental lines and selecting progeny that are genetically similar to the parental line. This process is repeated for multiple generations to transfer one or a few desired genes from a donor parent into the genome of a recurrent parental line. It allows for transferring traits like disease resistance between varieties while maintaining the desirable characteristics of the recurrent parent. The method is useful for transferring simply inherited traits and can be used to develop isogenic lines or convert germplasm for traits like photosensitivity.
Gregor Mendel conducted experiments on pea plants to study inheritance of traits from parents to offspring. He found that traits are controlled by factors now known as genes and alleles. A characteristic has two alleles, and offspring inherit one allele from each parent. If one allele is dominant, it suppresses the effect of the recessive allele. In Mendel's monohybrid crosses, the F1 generation showed only the dominant trait, while the F2 generation had a 3:1 ratio of dominant to recessive traits. Mendel's experiments formed the basis of classical genetics and laws of inheritance.
This document provides an overview of genetics and Mendelian inheritance. It discusses how Mendel conducted experiments on pea plants to develop the principles of heredity, including his laws of inheritance. Mendel showed that traits are inherited as discrete units (genes) that assort independently, with one trait (dominant) masking the expression of another (recessive) trait. His work demonstrated monohybrid and dihybrid crosses, and laid the foundations for modern genetics.
Principles of Inheritance, Class 12 CBSEblessiemary
This document provides information about principles of inheritance and variation in genetics. It discusses key topics including:
- Genetics deals with inheritance and variation from parents to offspring. Variation results in offspring differing from parents.
- Gregor Mendel conducted experiments with pea plants in the 1800s and established the principles of heredity, including dominance, segregation, independent assortment. He demonstrated genes are passed from parents to offspring in predictable ratios.
- Chromosomal theory of inheritance later explained that genes are located on chromosomes and segregate during gamete formation according to Mendel's laws. The work of Morgan, Sutton, and Boveri supported this theory through experimentation.
Gene interactions and multiple alleles.pptxSuryaCharan4
Gene interactions and multiple alleles control many traits in organisms. There are two main types of gene interaction - allelic/non-epistatic interaction which follows Mendelian ratios, and non-allelic/epistatic interaction where gene expression depends on other genes. Epistatic genes suppress others in traits like coat color. Multiple alleles originate from mutations at a locus and exist as allelic series like blood types (A, B, AB, O) and rabbit coat colors which are determined by multiple alleles at a gene locus.
This document discusses wide hybridization or distant hybridization, which involves crossing individuals from different plant species or genera. It describes the history and objectives of distant hybridization, as well as the types (interspecific, intergeneric), features, barriers, techniques to overcome barriers, applications in crop improvement, and limitations. Examples are provided of successful interspecific hybrids like Nerica rice and Triticale wheat-rye hybrids created using embryo rescue after intergeneric crosses. Barriers to distant hybridization include failure of zygote formation, zygote development, seedling development, and hybrid breakdown.
This document discusses distant hybridization, which involves crossing individuals from different plant species or genera. Some key points:
- The first recorded distant hybrid was between carnation and sweet william produced in 1717. An inter-generic hybrid called raphanobrassica was produced in 1928.
- Problems with distant hybrids include cross incompatibility, hybrid inviability, sterility, and breakdown in subsequent generations. Techniques like embryo rescue can help overcome some issues.
- Distant hybridization can be used to transfer beneficial traits like disease resistance between species. It has led to improvements in crops through hybrid varieties with increased yield, adaptation, and resistance to insects and disease.
1. The document discusses principles of inheritance and variation in biology, summarizing Mendel's experiments with pea plants and the conclusions he drew.
2. Mendel performed crosses involving seven traits of pea plants and found that traits are inherited in discrete units (now called genes) and that one allele is dominant over the recessive allele.
3. Through his experiments with monohybrid and dihybrid crosses, Mendel established the laws of segregation and independent assortment, showing that alleles segregate and are transmitted independently during gamete formation.
1) Mendel studied inheritance of traits in pea plants and developed the laws of genetics through extensive experimentation.
2) The Law of Segregation states that organisms pass one of two alleles to their offspring and these alleles segregate during gamete formation such that a cross between heterozygotes results in a 3:1 phenotypic ratio.
3) The Law of Independent Assortment demonstrated that two traits assort independently during gamete formation, resulting in a 9:3:3:1 phenotypic ratio for a dihybrid cross. Mendel's work laid the foundation for modern genetics.
B.tech biotech i bls u 4 mendal's geneticsRai University
Mendel conducted experiments with pea plants between 1856-1863. He found that traits are inherited in predictable patterns. Through crossbreeding plants with different traits like seed shape, color, plant height, he discovered that traits are controlled by factors (now called genes) which are inherited independently. His work established the laws of inheritance and formed the foundation of modern genetics.
The document discusses the process of developing commercial hybrid varieties through inbreeding. It involves three main steps - developing inbred lines through self-pollination over multiple generations, evaluating the inbred lines through tests like top cross testing and single cross evaluation, and producing hybrid seeds by crossing selected inbred lines. The hybrids derived from inbred lines are homogeneous and uniform, performing predictably, which makes them desirable for commercial production. Objections to the dominance hypothesis for heterosis are also addressed, with explanations like linkage and large number of genes governing traits resulting in symmetrical distributions.
This document discusses genetic linkage and mapping techniques in eukaryotes. It defines linkage as genes failing to assort independently due to being located near each other on the same chromosome. Morgan's experiments with Drosophila showed that alleles can be inherited together or recombine during meiosis. The frequency of recombination between two linked genes provides their genetic distance in centimorgans on a linkage map. Techniques for mapping genes include testcrosses, estimating recombination frequencies in two-point and three-point crosses, and correcting for double crossovers.
Crop improvement can be achieved through both sexual and asexual reproduction. Sexual reproduction combines genes from two parents, creating new combinations, while asexual reproduction clones the parent plant. Vegetative propagation methods include cuttings, grafting, and tissue culture. Genetic engineering allows for direct transfer of genes between organisms. Traditional breeding techniques also improve crops through selection of desirable traits over generations. [/SUMMARY]
Genetic variation refers to differences in genes between individuals of a population. It arises due to mutations, recombination during meiosis, gene flow between populations, and environmental factors. Genetic variation is important for evolution and survival of species as it provides raw materials for natural selection. While some genetic variations are harmful, others can provide benefits like disease resistance. Variations in genes involved in drug metabolism can impact individual responses to medications. Understanding genetic diversity is important for personalized medicine and drug development.
Backcross breeding is a method used to transfer one or few desirable traits from a donor parent to a recurrent parent with otherwise good qualities. It involves crossing a hybrid plant with one of its parents and selecting progeny that resemble the recurrent parent for further backcrossing. This helps recover most of the recurrent parent's genome while introducing the desired trait. Marker-assisted backcrossing can improve efficiency by selecting against donor genome regions outside the target locus and choosing rare recombinants near the target gene. The objective is to develop an improved variety like the recurrent parent but with the trait from the donor parent.
- Gregor Mendel conducted genetic experiments with pea plants to study heredity and traits such as plant height, flower color, seed shape and color. He found that traits are determined by discrete factors called genes.
- In his experiments, Mendel observed that some traits were dominant over others in hybrid offspring. When he allowed these hybrids to self-pollinate, the recessive traits that had been masked reappeared in a predictable ratio in the next generation.
- Mendel's experiments supported the idea that genes assort independently during reproduction, resulting in new combinations of traits in offspring. His findings established foundations of classical genetics and heredity.
Gregor Mendel conducted experiments with pea plants to study inheritance of traits. He found that traits are inherited based on discrete units called genes. Genes exist in pairs and can be dominant or recessive. Through his experiments with monohybrid and dihybrid crosses, Mendel discovered his two laws of inheritance - the Law of Segregation and the Law of Independent Assortment. These laws form the basis of modern genetics.
This document provides information about genetics and Mendelian inheritance. It begins with an introduction to important figures in the history of genetics like Gregor Mendel. It then discusses the three main theories of inheritance pre-Mendel and the history of genetics including Mendel's experiments and laws of inheritance. The rest of the document details various genetics concepts like linkage, crossing over, aneuploidy and their relationships to chromosomes and inheritance patterns.
The back cross method involves crossing a hybrid plant with one of its parental lines and selecting progeny that are genetically similar to the parental line. This process is repeated for multiple generations to transfer one or a few desired genes from a donor parent into the genome of a recurrent parental line. It allows for transferring traits like disease resistance between varieties while maintaining the desirable characteristics of the recurrent parent. The method is useful for transferring simply inherited traits and can be used to develop isogenic lines or convert germplasm for traits like photosensitivity.
Gregor Mendel conducted experiments on pea plants to study inheritance of traits from parents to offspring. He found that traits are controlled by factors now known as genes and alleles. A characteristic has two alleles, and offspring inherit one allele from each parent. If one allele is dominant, it suppresses the effect of the recessive allele. In Mendel's monohybrid crosses, the F1 generation showed only the dominant trait, while the F2 generation had a 3:1 ratio of dominant to recessive traits. Mendel's experiments formed the basis of classical genetics and laws of inheritance.
This document provides an overview of genetics and Mendelian inheritance. It discusses how Mendel conducted experiments on pea plants to develop the principles of heredity, including his laws of inheritance. Mendel showed that traits are inherited as discrete units (genes) that assort independently, with one trait (dominant) masking the expression of another (recessive) trait. His work demonstrated monohybrid and dihybrid crosses, and laid the foundations for modern genetics.
Principles of Inheritance, Class 12 CBSEblessiemary
This document provides information about principles of inheritance and variation in genetics. It discusses key topics including:
- Genetics deals with inheritance and variation from parents to offspring. Variation results in offspring differing from parents.
- Gregor Mendel conducted experiments with pea plants in the 1800s and established the principles of heredity, including dominance, segregation, independent assortment. He demonstrated genes are passed from parents to offspring in predictable ratios.
- Chromosomal theory of inheritance later explained that genes are located on chromosomes and segregate during gamete formation according to Mendel's laws. The work of Morgan, Sutton, and Boveri supported this theory through experimentation.
Gene interactions and multiple alleles.pptxSuryaCharan4
Gene interactions and multiple alleles control many traits in organisms. There are two main types of gene interaction - allelic/non-epistatic interaction which follows Mendelian ratios, and non-allelic/epistatic interaction where gene expression depends on other genes. Epistatic genes suppress others in traits like coat color. Multiple alleles originate from mutations at a locus and exist as allelic series like blood types (A, B, AB, O) and rabbit coat colors which are determined by multiple alleles at a gene locus.
This document discusses wide hybridization or distant hybridization, which involves crossing individuals from different plant species or genera. It describes the history and objectives of distant hybridization, as well as the types (interspecific, intergeneric), features, barriers, techniques to overcome barriers, applications in crop improvement, and limitations. Examples are provided of successful interspecific hybrids like Nerica rice and Triticale wheat-rye hybrids created using embryo rescue after intergeneric crosses. Barriers to distant hybridization include failure of zygote formation, zygote development, seedling development, and hybrid breakdown.
This document discusses distant hybridization, which involves crossing individuals from different plant species or genera. Some key points:
- The first recorded distant hybrid was between carnation and sweet william produced in 1717. An inter-generic hybrid called raphanobrassica was produced in 1928.
- Problems with distant hybrids include cross incompatibility, hybrid inviability, sterility, and breakdown in subsequent generations. Techniques like embryo rescue can help overcome some issues.
- Distant hybridization can be used to transfer beneficial traits like disease resistance between species. It has led to improvements in crops through hybrid varieties with increased yield, adaptation, and resistance to insects and disease.
1. The document discusses principles of inheritance and variation in biology, summarizing Mendel's experiments with pea plants and the conclusions he drew.
2. Mendel performed crosses involving seven traits of pea plants and found that traits are inherited in discrete units (now called genes) and that one allele is dominant over the recessive allele.
3. Through his experiments with monohybrid and dihybrid crosses, Mendel established the laws of segregation and independent assortment, showing that alleles segregate and are transmitted independently during gamete formation.
1) Mendel studied inheritance of traits in pea plants and developed the laws of genetics through extensive experimentation.
2) The Law of Segregation states that organisms pass one of two alleles to their offspring and these alleles segregate during gamete formation such that a cross between heterozygotes results in a 3:1 phenotypic ratio.
3) The Law of Independent Assortment demonstrated that two traits assort independently during gamete formation, resulting in a 9:3:3:1 phenotypic ratio for a dihybrid cross. Mendel's work laid the foundation for modern genetics.
B.tech biotech i bls u 4 mendal's geneticsRai University
Mendel conducted experiments with pea plants between 1856-1863. He found that traits are inherited in predictable patterns. Through crossbreeding plants with different traits like seed shape, color, plant height, he discovered that traits are controlled by factors (now called genes) which are inherited independently. His work established the laws of inheritance and formed the foundation of modern genetics.
The document discusses the process of developing commercial hybrid varieties through inbreeding. It involves three main steps - developing inbred lines through self-pollination over multiple generations, evaluating the inbred lines through tests like top cross testing and single cross evaluation, and producing hybrid seeds by crossing selected inbred lines. The hybrids derived from inbred lines are homogeneous and uniform, performing predictably, which makes them desirable for commercial production. Objections to the dominance hypothesis for heterosis are also addressed, with explanations like linkage and large number of genes governing traits resulting in symmetrical distributions.
This document discusses genetic linkage and mapping techniques in eukaryotes. It defines linkage as genes failing to assort independently due to being located near each other on the same chromosome. Morgan's experiments with Drosophila showed that alleles can be inherited together or recombine during meiosis. The frequency of recombination between two linked genes provides their genetic distance in centimorgans on a linkage map. Techniques for mapping genes include testcrosses, estimating recombination frequencies in two-point and three-point crosses, and correcting for double crossovers.
Crop improvement can be achieved through both sexual and asexual reproduction. Sexual reproduction combines genes from two parents, creating new combinations, while asexual reproduction clones the parent plant. Vegetative propagation methods include cuttings, grafting, and tissue culture. Genetic engineering allows for direct transfer of genes between organisms. Traditional breeding techniques also improve crops through selection of desirable traits over generations. [/SUMMARY]
Genetic variation refers to differences in genes between individuals of a population. It arises due to mutations, recombination during meiosis, gene flow between populations, and environmental factors. Genetic variation is important for evolution and survival of species as it provides raw materials for natural selection. While some genetic variations are harmful, others can provide benefits like disease resistance. Variations in genes involved in drug metabolism can impact individual responses to medications. Understanding genetic diversity is important for personalized medicine and drug development.
Backcross breeding is a method used to transfer one or few desirable traits from a donor parent to a recurrent parent with otherwise good qualities. It involves crossing a hybrid plant with one of its parents and selecting progeny that resemble the recurrent parent for further backcrossing. This helps recover most of the recurrent parent's genome while introducing the desired trait. Marker-assisted backcrossing can improve efficiency by selecting against donor genome regions outside the target locus and choosing rare recombinants near the target gene. The objective is to develop an improved variety like the recurrent parent but with the trait from the donor parent.
- Gregor Mendel conducted genetic experiments with pea plants to study heredity and traits such as plant height, flower color, seed shape and color. He found that traits are determined by discrete factors called genes.
- In his experiments, Mendel observed that some traits were dominant over others in hybrid offspring. When he allowed these hybrids to self-pollinate, the recessive traits that had been masked reappeared in a predictable ratio in the next generation.
- Mendel's experiments supported the idea that genes assort independently during reproduction, resulting in new combinations of traits in offspring. His findings established foundations of classical genetics and heredity.
Gregor Mendel conducted experiments with pea plants to study inheritance of traits. He found that traits are inherited based on discrete units called genes. Genes exist in pairs and can be dominant or recessive. Through his experiments with monohybrid and dihybrid crosses, Mendel discovered his two laws of inheritance - the Law of Segregation and the Law of Independent Assortment. These laws form the basis of modern genetics.
Similar to PLANT BREEDING: backcross breeding, heterosis and their genetic basis. (20)
The ability to recreate computational results with minimal effort and actionable metrics provides a solid foundation for scientific research and software development. When people can replicate an analysis at the touch of a button using open-source software, open data, and methods to assess and compare proposals, it significantly eases verification of results, engagement with a diverse range of contributors, and progress. However, we have yet to fully achieve this; there are still many sociotechnical frictions.
Inspired by David Donoho's vision, this talk aims to revisit the three crucial pillars of frictionless reproducibility (data sharing, code sharing, and competitive challenges) with the perspective of deep software variability.
Our observation is that multiple layers — hardware, operating systems, third-party libraries, software versions, input data, compile-time options, and parameters — are subject to variability that exacerbates frictions but is also essential for achieving robust, generalizable results and fostering innovation. I will first review the literature, providing evidence of how the complex variability interactions across these layers affect qualitative and quantitative software properties, thereby complicating the reproduction and replication of scientific studies in various fields.
I will then present some software engineering and AI techniques that can support the strategic exploration of variability spaces. These include the use of abstractions and models (e.g., feature models), sampling strategies (e.g., uniform, random), cost-effective measurements (e.g., incremental build of software configurations), and dimensionality reduction methods (e.g., transfer learning, feature selection, software debloating).
I will finally argue that deep variability is both the problem and solution of frictionless reproducibility, calling the software science community to develop new methods and tools to manage variability and foster reproducibility in software systems.
Exposé invité Journées Nationales du GDR GPL 2024
ESPP presentation to EU Waste Water Network, 4th June 2024 “EU policies driving nutrient removal and recycling
and the revised UWWTD (Urban Waste Water Treatment Directive)”
The use of Nauplii and metanauplii artemia in aquaculture (brine shrimp).pptxMAGOTI ERNEST
Although Artemia has been known to man for centuries, its use as a food for the culture of larval organisms apparently began only in the 1930s, when several investigators found that it made an excellent food for newly hatched fish larvae (Litvinenko et al., 2023). As aquaculture developed in the 1960s and ‘70s, the use of Artemia also became more widespread, due both to its convenience and to its nutritional value for larval organisms (Arenas-Pardo et al., 2024). The fact that Artemia dormant cysts can be stored for long periods in cans, and then used as an off-the-shelf food requiring only 24 h of incubation makes them the most convenient, least labor-intensive, live food available for aquaculture (Sorgeloos & Roubach, 2021). The nutritional value of Artemia, especially for marine organisms, is not constant, but varies both geographically and temporally. During the last decade, however, both the causes of Artemia nutritional variability and methods to improve poorquality Artemia have been identified (Loufi et al., 2024).
Brine shrimp (Artemia spp.) are used in marine aquaculture worldwide. Annually, more than 2,000 metric tons of dry cysts are used for cultivation of fish, crustacean, and shellfish larva. Brine shrimp are important to aquaculture because newly hatched brine shrimp nauplii (larvae) provide a food source for many fish fry (Mozanzadeh et al., 2021). Culture and harvesting of brine shrimp eggs represents another aspect of the aquaculture industry. Nauplii and metanauplii of Artemia, commonly known as brine shrimp, play a crucial role in aquaculture due to their nutritional value and suitability as live feed for many aquatic species, particularly in larval stages (Sorgeloos & Roubach, 2021).
BREEDING METHODS FOR DISEASE RESISTANCE.pptxRASHMI M G
Plant breeding for disease resistance is a strategy to reduce crop losses caused by disease. Plants have an innate immune system that allows them to recognize pathogens and provide resistance. However, breeding for long-lasting resistance often involves combining multiple resistance genes
ANAMOLOUS SECONDARY GROWTH IN DICOT ROOTS.pptxRASHMI M G
Abnormal or anomalous secondary growth in plants. It defines secondary growth as an increase in plant girth due to vascular cambium or cork cambium. Anomalous secondary growth does not follow the normal pattern of a single vascular cambium producing xylem internally and phloem externally.
EWOCS-I: The catalog of X-ray sources in Westerlund 1 from the Extended Weste...Sérgio Sacani
Context. With a mass exceeding several 104 M⊙ and a rich and dense population of massive stars, supermassive young star clusters
represent the most massive star-forming environment that is dominated by the feedback from massive stars and gravitational interactions
among stars.
Aims. In this paper we present the Extended Westerlund 1 and 2 Open Clusters Survey (EWOCS) project, which aims to investigate
the influence of the starburst environment on the formation of stars and planets, and on the evolution of both low and high mass stars.
The primary targets of this project are Westerlund 1 and 2, the closest supermassive star clusters to the Sun.
Methods. The project is based primarily on recent observations conducted with the Chandra and JWST observatories. Specifically,
the Chandra survey of Westerlund 1 consists of 36 new ACIS-I observations, nearly co-pointed, for a total exposure time of 1 Msec.
Additionally, we included 8 archival Chandra/ACIS-S observations. This paper presents the resulting catalog of X-ray sources within
and around Westerlund 1. Sources were detected by combining various existing methods, and photon extraction and source validation
were carried out using the ACIS-Extract software.
Results. The EWOCS X-ray catalog comprises 5963 validated sources out of the 9420 initially provided to ACIS-Extract, reaching a
photon flux threshold of approximately 2 × 10−8 photons cm−2
s
−1
. The X-ray sources exhibit a highly concentrated spatial distribution,
with 1075 sources located within the central 1 arcmin. We have successfully detected X-ray emissions from 126 out of the 166 known
massive stars of the cluster, and we have collected over 71 000 photons from the magnetar CXO J164710.20-455217.
Remote Sensing and Computational, Evolutionary, Supercomputing, and Intellige...University of Maribor
Slides from talk:
Aleš Zamuda: Remote Sensing and Computational, Evolutionary, Supercomputing, and Intelligent Systems.
11th International Conference on Electrical, Electronics and Computer Engineering (IcETRAN), Niš, 3-6 June 2024
Inter-Society Networking Panel GRSS/MTT-S/CIS Panel Session: Promoting Connection and Cooperation
https://www.etran.rs/2024/en/home-english/
Nucleophilic Addition of carbonyl compounds.pptxSSR02
Nucleophilic addition is the most important reaction of carbonyls. Not just aldehydes and ketones, but also carboxylic acid derivatives in general.
Carbonyls undergo addition reactions with a large range of nucleophiles.
Comparing the relative basicity of the nucleophile and the product is extremely helpful in determining how reversible the addition reaction is. Reactions with Grignards and hydrides are irreversible. Reactions with weak bases like halides and carboxylates generally don’t happen.
Electronic effects (inductive effects, electron donation) have a large impact on reactivity.
Large groups adjacent to the carbonyl will slow the rate of reaction.
Neutral nucleophiles can also add to carbonyls, although their additions are generally slower and more reversible. Acid catalysis is sometimes employed to increase the rate of addition.
Phenomics assisted breeding in crop improvementIshaGoswami9
As the population is increasing and will reach about 9 billion upto 2050. Also due to climate change, it is difficult to meet the food requirement of such a large population. Facing the challenges presented by resource shortages, climate
change, and increasing global population, crop yield and quality need to be improved in a sustainable way over the coming decades. Genetic improvement by breeding is the best way to increase crop productivity. With the rapid progression of functional
genomics, an increasing number of crop genomes have been sequenced and dozens of genes influencing key agronomic traits have been identified. However, current genome sequence information has not been adequately exploited for understanding
the complex characteristics of multiple gene, owing to a lack of crop phenotypic data. Efficient, automatic, and accurate technologies and platforms that can capture phenotypic data that can
be linked to genomics information for crop improvement at all growth stages have become as important as genotyping. Thus,
high-throughput phenotyping has become the major bottleneck restricting crop breeding. Plant phenomics has been defined as the high-throughput, accurate acquisition and analysis of multi-dimensional phenotypes
during crop growing stages at the organism level, including the cell, tissue, organ, individual plant, plot, and field levels. With the rapid development of novel sensors, imaging technology,
and analysis methods, numerous infrastructure platforms have been developed for phenotyping.
Comparing Evolved Extractive Text Summary Scores of Bidirectional Encoder Rep...University of Maribor
Slides from:
11th International Conference on Electrical, Electronics and Computer Engineering (IcETRAN), Niš, 3-6 June 2024
Track: Artificial Intelligence
https://www.etran.rs/2024/en/home-english/
PLANT BREEDING: backcross breeding, heterosis and their genetic basis.
1. PLANTBREEDING
Submitted to Submitted by
Merin Alice Jacob Krishnapriya M
Assistant Professor Roll. No:10
Dept. of Botany 1st M.Sc. Botany
St. Teresa’s College, Ernakulam St. Teresa’s College, Ernakulam
1
2. BACKCROSSBREEDING
• Backcross is the crossing of an F1 hybrid with one or other of it’s parents.
• But in plant breeding. Backcross method involves crossing of an F1 hybrid
with it’s superior parent whose genotype has to be transferred to local
variety.
• Backcrosses are usually used to impart to a local variety one or more
desirable characters inherent in another variety, without disturbing genetic
integrity of former.
• Here, recipient parent is used repeatedly to get all desired genes from donor
parent.
• Recipient parent is called recurrent parent and donor parent is called non-
recurrent parent.
2
3. • The F1 hybrids and subsequent generations, which have acquired foreign
genes from donor, may be crossed again with recurrent parent.
• Backcrossing is most used to eliminate a defect (susceptible to disease) from
a variety which has a set of desirable characters.
• The hybrids have to be crossed with recurrent parent over and again in order
to get rid of undesirable properties of parental form.
• During the process, recurrent parent’s genotype is restored in hybrid
progenies and undesirable genes of donor get eliminated.
• So, segregation becomes more simple.
• As a rule, five or six backcrosses are sufficient for nearly complete transfer
of desirable characters.
• In some cases, ten backcrosses are used.
3
4. BACKCROSSBREEDINGPROCEDURES
1. Selection of parents :
• The recurrent parent (parent A) is most popular variety of region.
• The donor parent (parent B) should possess character desired to be
transferred in genetic background of recurrent parent (A).
• It must be controlled by one or other major genes.
2. Dominant gene controlled character :
• If the character to be transferred in genetic background of recurrent parent
(A) is governed by a dominant gene.
• Then F1of cross (A×B) could be backcrossed to recurrent parent (A)
successively up to BC4-BC5 generations.
4
5. • Thereafter, F2 and F3 generations should be raised and selection of new
genotype lines having restored almost 99% of agronomic traits of recurrent
parent plus one character transferred from donor parent B.
• After purification, homozygous lines should be bulked and tested in progeny
row trials for one year along with recurrent parent as check to transfer
desired character.
• There is no need to raise F2 and F3 generations in initial backcross
generation (BC1, BC2, BC3 and BC4) because in every backcross
generation, the dominant character is visible.
5
6. 3. Recessive gene controlled character :
• In cases, where character desired under transfer is controlled by recessive
gene, in F1 generation it is not visible, hence breeder has to raise F2 and F3
generations after each backcross .
• Selection of desired genotypes should be done to each backcross generation.
• eg: BC1= The F1 of cross A×B.
• F1 is backcrossed to A (recurrent parent).
• The seeds of BC1 plants are selfed to produce F2 population (1500-2000
plants) in which intensive seed is done for desired character of donor parent
‘B’ combined with general characters of recurrent parent A.
• The selected plants are raised to produce F3 lines, among and within F3 lines
, selected plants recover traits of recurrent parent.
6
7. HETEROSIS
• The term heterosis was first used by Shull in 1914.
• It is also called as true heterosis or euheterosis.
• It is defined as superiority of an F1 hybrid over both it’s parents in terms of
yield or some other character.
• Heterosis is manifested as an increase in vigour, size, growth rate, yield or
some other characteristics.
• But in some cases, hybrid may be inferior to weaker parent. This is also
regarded as heterosis.
• Often the superiority of F1 is estimated over average of two parents or mid-
parent.
7
8. • If the hybrid is superior to mid-parent, it is known as average or relative
heterosis.
• If the hybrid is superior over superior parent =heterobeltiosis.
• Powers suggested that term heterosis should be used only when hybrid is
either superior or inferior to both parents.
• A/C to this, heterosis is the superiority of F1 hybrid over mid-parent and
heterobeltiosis is the superiority of F1 hybrid over superior parent.
8
9. MANIFESTATIONSOFHETEROSIS
a) Increased Yield:
• Heterosis is expressed as increase in yield of hybrids.
• Higher yields are most important objective of plant breeding.
• The yield may be measured in terms of grain, fruit, seed, leaf, tubers or the
whole plant.
b) Increased Reproductive Ability:
• The hybrids exhibiting heterosis show an increase in fertility or reproductive
ability.
• Higher yield of seeds or fruits or other propagules, stem in sugarcane etc.
9
10. c) Increase in Size and General Vigour:
• Hybrids are generally more vigorous ie, healthier and faster growing and
larger in size than their parents.
• The increase in size is usually a result of increase in number and size of cells
in various plant parts.
Eg: increased size in tomato, head size in cabbage, cob size in maize etc.
d) Better Quality:
• In many cases, hybrids show improved quality.
• This may or may not be accompanied by higher yields.
Eg: many hybrids in onion show better keeping quality but not yield, than open
pollinated varieties.
10
11. e) Earlier Flowering and Maturity:
• In many cases, hybrids are earlier in flowering and maturity than parents.
• This may associate with lower total plant weight.
• But earliness is highly desirable in many cases, particularly vegetables.
• Many tomato hybrids are earlier than their parents.
f) Greater Resistance to Diseases and Pests:
• Some hybrids are known to exhibit a greater resistance to insects or diseases
than their parents.
g) Greater Adaptability:
• Hybrids are more adapted to environmental changes than inbreds.
• Variance of hybrids is smaller than inbreds.
11
12. h) Faster Growth Rate:
• Hybrids show faster growth rate than their parents.
• But total plant size of hybrids may be comparable to that of parents.
• Faster growth rate is not associated with larger size.
i) Increase in Number of a Plant Part:
• There is an increase in number of nodes, leaves and other plant parts.
• But total plant size may not be larger.
Eg: hybrids in beans.
j) Manifestation at Molecular Level:
• Increased rate of DNA duplication, genetic transcription, genetic translation
and enzyme activity.
12
13. k) Manifestation at Metabolic Level:
• Increased and effective co-ordination and regulation of metabolic processes
and morphogenetic events.
l) Manifestation at Cellular Level:
• Increased rate of cell proliferation.
m) Manifestation at Organismal Level:
• High rate of cellular growth and differentiation, increased synthesis,
accumulation and utilization of substances etc.
13
14. GENETICBASISOFHETEROSISANDINBREEDINGDEPRESSION
1. DOMINANCE HYPOTHESIS
• First proposed by Davenport in 1908.
• Later expanded by Bruce, Keeble and Pellew in 1910.
• Hypothesis suggest that at each locus the dominant allele has a favourable
effect, while the recessive allele has an unfavourable effect.
• In heterozygous state, deleterious effects of recessive alleles are masked by
their dominant alleles.
• Thus, heterosis results from masking of harmful effects of recessive alleles
by their dominant alleles.
• Inbreeding depression – due to harmful effects of recessive alleles, which
become homozygous due to inbreeding.
14
15. A/c to this,
• Heterosis is not a result of heterozygosity.
• It is the result of prevention of expression of harmful recessives by their
dominant alleles.
• Inbreeding depression does not result from homozygosity but from
homozygosity of recessive alleles, which have harmful effects.
eg: In open-pollinated populations, plants are highly heterozygous.
• So, they do not show harmful effects of large number of deleterious
recessive alleles present in population.
• Inbreeding increases homozygosity. So, many recessive alleles become
homozygous.
• Lethal recessive alleles are eliminated by natural selection. But recessive
alleles with smaller harmful effects survive in homozygous condition.
15
16. • Such alleles reduce vigour and fertility of inbred lines that carry them in the
homozygous state.
• Inbred lines are nearly homozygous and different inbred lines would receive
different proportions of dominant and recessive alleles.
• Different inbred lines vary in vigour and yield.
• It should be possible to isolate such inbreds that have all dominant alleles
present in population.
• Such inbreds will be vigorous as open pollinated varieties.
• But such inbreds have not been isolated yet.
16
17. OBJECTIONS
a) Failure in the Isolation of Inbreds as Vigorous as Hybrids :
• A/c to this hypothesis, it should be possible to isolate inbreds with all
dominant genes.
• Such inbreds would be vigorous as F1 hybrids.
• But such inbreds are not isolated yet.
b) Symmetrical Distribution in F2 :
• In F2, dominant and recessive characters segregate in ratio of 3:1.
• A/c to this, quantitative characters should not show symmetrical distribution
in F2.
• This is because dominant and recessive phenotypes would segregate in
proportion (3/4 +1/4)^n.
17
18. • n is number of genes segregating.
c) Magnitude of Heterosis :
• The inbred lines have improved in terms of per sec performance over
decades.
• If dominance were main cause of heterosis, magnitude of heterosis generated
by such inbreds should have declined.
d) Progressive Heterosis in Tetraploids :
• In autotetraploids, hybrids between two inbred lines show heterosis.
• Such hybrids have genotype A1A1A2A2 at a given locus.
• But tetraploid hybrids have genotypes A1A2A2A3, A1A1A2A3 etc (three
different alleles) and A1A2A3A4 ( 4 different alleles) show greater heterosis
than A1A1A2A2 (2 different alleles).
18
19. 2. OVERDOMINANCE HYPOTHESIS
• Proposed by East and Shull in 1908.
• Also known as single gene heterosis, super dominance, cumulative action of
divergent alleles and stimulation of divergent alleles.
• The idea of super dominance, ie, heterozygote superiority was put forth by
Fisher in 1903 and was later elaborated by East and Shull.
• A/c to this, in heterozygotes at least some of loci are superior to both
relevant homozygotes.
• Thus heterozygote Aa would be superior to both homozygotes AA and aa.
• Heterozygosity is essential for and is cause of heterosis.
• Homozygosity resulting from inbreeding produces inbreeding depression.
19
20. • In 1936, East proposed that at each locus showing over dominance, there are
several alleles ie, a1, a2, a3, a4….etc with increasingly different functions.
• He also proposed that heterozygotes for more divergent alleles would be
more heterotic than those involving less divergent ones.
Eg: a1a4 would be superior to a1a2, a2a3 or a3a4.
Eg: In case of maize, gene ma affects maturity. The heterozygote Ma ma is
more vigorous than homozygotes Ma Ma and ma ma.
Eg: Gustafsson reported two chlorophyll mutants in barley that produce
larger and more number of seeds in heterozygous state than do their normal
homozygotes.
20
21. PHYSIOLOGICALHYPOTHESIS
a) Nucleo-cytoplasmic interaction hypothesis :
• Proposed independently by Shull, Michalis and others.
• States that heterosis results from nucleo-cytoplasmic interactions which
involves effect of changed nucleus on unchanged cytoplasm and vice-versa.
b) Greater initial capital hypothesis :
• Put forward by Ashby in 1930.
• Holds that heterosis is due to greater initial size of embryo.
21
22. INBREEDING
• Inbreeding or consanguinous mating is mating between individuals related
by descent or ancestry or it is the form of controlled breeding between
genetically related individuals of species.
• When individuals are closely related, eg: in brother-sister mating or sib-
mating, degree of inbreeding is high.
• The highest degree of inbreeding is achieved by selfing.
• The chief effect of inbreeding is an increase in homozygosity in progeny,
which is proportionate to degree of inbreeding.
• The measure of degree of inbreeding is provided by degree of homozygosity
in progeny.
22
23. For example:
• Selfing reduces heterozygosity by a factor of ½ in each generation.
• The degree of inbreeding increases in the same proportion.
• Degree of inbreeding in any generation is equal to degree of homozygosity in
that generation.
• Inbreeding differs from outbreeding : Outbreeding promotes heterozygosity
and introduce new genes into the population.
• Most genes of undesirable or harmful traits are recessive and are only
expressed in homozygous condition.
• Thus, inbreeding promotes expression of harmful traits in progeny.
• This enables to sort out and exclude individuals with undesirable characters
from breeding practices. Thus careful selection is carried out.
23
24. • The degree of inbreeding of an individual is expressed as inbreeding
coefficient (F).
• The value of F for an individual = probability of two alleles of a gene present
in that individual to have been derived from a single allele of a common
ancestor.
eg: an ancestor that occurs in the pedigree of both maternal and paternal
parents of this individual.
• In a random mating population, the value of F for any individual is 0.
• While, that for an individual produced by selfing of a plant from a random
mating population is ½.
• The value of F is cumulative over generations.
24
25. INBREEDINGDEPRESSION
• It is defined as reduction or loss in vigour and fertility as a result of
inbreeding.
• Or continued inbreeding in regular succession may lead to progressive
decrease in growth, size, vigour, fitness and fertility of offspring.
• The degree of inbreeding depression depends on plant species concerned.
• But within a species, extent of depression is related to value of F.
• Inbreeding depression is common in case of such traits that form an
important component of fitness, while those that contribute little to fitness
usually show little or no inbreeding depression.
• The extent of inbreeding depression is not same in all lines produced by
inbreeding.
25
26. • After several generations of inbreeding, a stage may be reached beyond
which no further inbreeding depression occurs.
• This stage is called inbreeding minimum.
• The crossing of inbred lines, which have reached inbreeding minimum, often
results in heterosis.
26
27. DEGREE OF INBREEDING DEPRESSION
a) High Inbreeding Depression
• Several plant species eg: alfafa (Medicago sativa), carrot ( Daucus carota) etc
show very high inbreeding depression.
• A large proportion of plants produced by selfing show lethal characteristics
and do not survive.
• The loss in vigour and fertility is so great that very few lines can be
maintained after 3-4 generations of inbreeding.
• The lines that do not survive show greatly reduced yields, generally less than
25% of yield of open-pollinated varieties.
27
28. b) Moderate Inbreeding Depression
• Many crop species, such as maize (Zea mays ), jowar, bajra etc show
moderate inbreeding depression.
• Selfing of progeny result in 2 types of individual i) normal types and ii)
weak, sublethal or lethal types.
• There is appreciable reduction in fertility and many lines reproduce so
poorly that they are lost. Elimination of 2nd category maintain population.
• However, large number of inbred lines can be obtained, which yield up to
50% of open-pollinated varieties.
• Production and maintenance of inbred lines are relatively easier in these
species than in those showing a high degree of inbreeding.
28
29. c) Low Inbreeding Depression
• Several crop plants eg: onion, many cucurbits, rye, sunflower etc show only
a small degree of inbreeding depression.
• Only a small proportion of plants show lethal characteristics.
• The loss in vigour and fertility is small, rarely a line cannot be maintained
due to poor fertility.
• The reduction in yield due to inbreeding is small or absent.
• Some of inbred lines may yield as much as open pollinated varieties from
which they were developed.
29
30. d) Zero Inbreeding Depression
• Self-pollinates progeny does not exhibit any effect of inbreeding depression.
• But shows some degree of heterosis.
• It is because these species reproduce by self fertilization and as a result, have
developed homozygous balance.
• In contrast, cross pollinated species exhibit heterozygous balance.
30
31. IDEOTYPEBREEDING
• The term was introduced by Donald (1968).
• It is defined as a biological model, which is expected to perform or behave in
a particular manner within a defined environment.
• A/c to him, ‘ a crop ideotype is a plant model, which is expected to yield a
greater quantity or quality of grain, oil or other useful product when
developed as a cultivar’.
• It is also known as model plant type, ideal model plant type and ideal plant
type.
• In general terms, an ideotype is a conceptual model plant, which has all such
characteristics that are considered ideal for given environment.
• A model plant is optimally equipped for maximum yield under defined
environment.
31
32. TYPESOFIDEOTYPE
a) Isolation Ideotype
• It is the model plant that performs best when plants are space-planted.
• In cereals, isolation ideotype is lax, free-tillering, leafy, spreading plant ie,
able to explore environment as fully as possible.
• It is unlikely to perform well at crop densities.
b) Competition Ideotype
• This ideotype performs well in genetically heterogenous poipulations, such
as segregating generation of crosses.
• In case of cereals, competition ideotype is tall, leafy, free-tillering plant ie,
able to shade it’s less aggressive neighbours and gain larger share of
nutrients and water.
32
33. c) Crop Ideotype
• This ideotype performs best at commercial crop densities because it is a poor
competitor.
• It performs well when it is surrounded by plants of same forms.
• But it performs less well when it is surrounded by plants of other forms.
33
34. FEATURESOFIDEOTYPEBREEDING
1. Emphasis on Individual Trait:
• Emphasis is given on individual morphological and physiological trait which
enhances yield.
• The value of each character is specified before initiating breeding work.
2. Includes Yield Enhancing Traits:
• Various plant characters to be included in ideotype are identified through
correlation analysis.
• Only those characters which exhibit positive association with yield are
included in the model.
34
35. 3. Exploits Physiological Variation:
• Genetic difference exists for various physiological characters such as
photosynthetic efficiency, photo respiration, nutrient uptake etc.
• Ideotype breeding makes use of genetically controlled physiological
variation in increasing crop yields, besides various agronomic traits.
4. Slow Progress:
• Ideotype breeding is a slow method of cultivar development because
incorporation of various desirable characters from different sources into a
single genotype takes long time.
• More over, sometimes undesirable linkage affects progress adversely.
35
36. 5. Selection:
• In ideotype breeding selection is focused on individual plant character which
enhances yields.
6. Designing of Model:
• Here, the phenotypes of new variety to be developed is specified in terms of
morphological and physiological traits in advance.
7. Interdisciplinary Approach:
• Ideotype breeding is in true sense an interdisciplinary approach.
• It involves scientist from disciplines of genetics, breeding, physiology,
pathology, entomology etc.
36
37. 8. A Continuous Process:
• It is a continuous process, because new ideotype have to be developed to
meet changing and increasing demands.
• Thus development of ideotype is a moving target.
• Ideotype breeding differs from traditional breeding in the sense that values
for individual traits are specified in case of ideotype breeding.
• Whereas such values are not fixed and then efforts are made to achieve such
model.
• In traditional breeding, such models are not developed before initiation of
breeding programmes.
37
38. METHODSOFIDEOTYPEBREEDING
Ideotype breeding consists of four important steps
1. Development of conceptual theoretical model.
2. Selection of base material.
3. Incorporation of desirable characters into single genotype.
4. Selection of ideal or model plant type.
38
39. 1.Development of Conceptual Model:
• Ideotype consists of various morphological and physiological traits.
• The values of various morphological and physiological traits are specified to
develop a conceptual theoretical model.
Eg: Value for plant height, maturity duration, leaf size, leaf number, angle of
leaf, photosynthetic rate etc are specified.
2. Selection of Base Material:
• Selection of base material is an important step after development of
conceptual model of ideotype.
• Genotype to be used in devising a model plant type should have broad
genetic base and wider adaptability.
• So that new plant type can be successfully grown over a wide range of
environmental condition with stable yield.
39
40. • Genotypes for plant stature, mature duration, leaf size and angles are selected
from global gene pool of concerned crop species.
• Genotypes resistant or tolerant to drought, soil salinity, alkalinity, disease and
insects are selected from gene pool with cooperation of physiologist, soil
scientist, pathologist and entomologist.
3. Incorporation of Desirable Traits:
• The next important step is combining of various morphological and
physiological traits from different selected genotypes into single genotype.
• Knowledge of association between various characters is essential before
starting hybridization programme, because it help in combining of various
characters.
40
41. • Linkage between procedures, viz single cross, three way cross, multiple
cross, composite crossing, backcross.
Eg: Mutation breeding, heterosis breeding etc. are used for development of
ideal plant types in majority of field crops.
• Backcross technique is commonly used for transfer of oligogenic traits from
selected germplasm lines into background of an adapted genotype.
4. Selection of Ideal Plant Type:
• Plant combining desirable morphological and physiological traits are
selected in segregating population and intermated to achieve desired plant
type.
• Morphological features are judged through visual observation and
physiological parameters are recorded with help of sophisticated instruments.
41
42. • Screening for resistance to drought, soil salinity, alkalinity, disease and
insects is done under controlled conditions.
• This task is completed with help of scientist from disciplines of physiology,
soil science, pathology and entomology.
• Finally, genotypes combining traits specified in conceptual model are
selected, multiplied, tested over several locations and released for
commercial cultivation.
42
43. APPLICATIONSOFIDEOTYPEBREEDING
1. WHEAT
• A short strong stem. It imparts lodging resistance and reduces losses due to
lodging.
• Erect leaves. Such leaves provide better arrangement for proper light
distribution resulting in high photosynthesis or co2 fixation.
• Few small leaves. Leaves are important sites of photosynthesis, respiration
and transpiration. Few and small reduce water loss due to transpiration.
• Larger ear. It will produce more grains per year.
• A presence of awns. Awns contribute towards photosynthesis.
• Single culm.
43
44. 2. MAIZE
• In 1975, Mock and Pearce proposed ideal plant type of maize.
• In maize, higher yields were obtained from plants consisting of
i. Low tillers.
ii. Large cobs.
iii. Angled leaves for good light interception. Planting of such type at closer
spacing resulting in higher yields.
44
45. 3. COTTON
• Short stature (90-120cm).
• Compact and sympodial plant habit making pyramidal shape.
• Determinate the fruiting habit with unimodal distribution of bolling.
• Short duration (150-165 days).
• Responsive to high fertilizer dose.
• High degree of inter plant competitive ability.
• High degree of resistance to insect pests and diseases.
• High physiological efficiency.
45
46. 4. CHICKPEA –RAINFED CONDITION
• Early vigour.
• 50-60cm plant height with 9-10 secondary branches.
• Tall, erect or semi-erect plant.
• More number of pods per plant.
• Podding from 10th node.
46
47. 5. CHICKPEA- IRRIGATED CONDITION
• High input responsiveness.
• Tall (75-90cm) and erect habit with broom shaped branching behaviour.
• Synchronous flowering, delayed senescence and determinancy.
• Long fruiting branches and short internodes.
• Lodging resistance.
• Pod bearing from 20cm above ground.
47
48. 6. PIGEON PEA
• Long and medium duration.
• Semi-dwarf plant type (1.5-1.8m) for mechanized plant protection.
• Open canopy with determinancy.
• Non-cluster pod bearing.
• Long fruiting branches for high yield.
• Middle and top bearing.
• Spreading type for intercropping in south and central india.
• Compact plant type for intercropping in northern india.
48
49. REFERENCES
1. Ram, M. ( 1982 ). Plant Breeding Methods. PHI Learning Pvt.ltd, Delhi.
2. Singh, B. D. (1983). Plant Breeding. Kalyani Publishers, New Delhi.
3. Singh, B. D. ( 2000). Plant Breeding Principles and Methods. Kalyani
Publishers, New Delhi.494949
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