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Centre of origin are also known as centre of diversity. N. I. Vavilov in 1926 has proposed that crop plants evolved from wild species in the areas showing diversity and termed them as primary centers of origin. Primary centers, crops moved to other areas with the movements of man. But in some areas, certain crop species show considerable diversity of forms although they did not originate there. Such areas are known as secondary centers of origin of these species. Genetic diversity is essential for crop improvement. Vavilov has suggested eight main centers of origin of crop plants.

1. Chinese Centre

This centre is considered to be one of the earliest and largest independent center of origin of cultivated plants. This centre includes mountain regions of central and western China. The endemic species listed from this centre include, soya bean, radish, turnip, pear, peach, plum, colocasia, buckwheat, opium poppy, brinjal, apricots, oranges, china tea etc.

2. Himalayan Centre

This centre is also known as the Indian centre of origin. This centre includes regions of Assam, Burma, Indo-china and Malayan Archipelago. The crops originated from this centre are rice, red gram, chick pea, pea, mung, brinjal, cucumber, sugar cane, black pepper, moth bean, rice bean, cotton, turmeric, indigo, millets etc.

The place of origin of the crop plant can be found out on the basis of genetic affinities. This would mean to find out the geographical distribution of the wild progenitors of the cultivated plants. If one can locate the distribution of a given progenitor, one can delimit the area in which domestication could have occurred. Vavilov based his judgment on variation patterns in cultivated plants. Information on wild plants in those days was much more fragmentary than what it is today. Even today, genetic and ecological information on wild relatives of several cultivated plants is incomplete and in such cases assessment of a place of origin is difficult to make. However, in most cases required information is available on genetic affinities between wild and tame, on distribution areas and on ecological affinities of the wild progenitors. On this basis it is possible to determine the initial place of origin.

Crop Domestication

Domestication can be loosely defined as the process of bringing of a wild species under the management of man. Domestication is the process by which genetic changes (or shifts) in wild plants are brought about through a selection process imposed by humans. Because of the role of humans, the process results in characteristics that are beneficial to humans but some that would be disadvantageous for plants in their natural habitats. It is an evolutionary process in which selection (both natural (frost tolerance) and artificial (large attractive fruits)) operates to change plants genetically, morphologically, and physiologically. 

Centrifugation is a technique that promotes accelerated settling of particles in a solid-liquid mixture by the application of centrifugal force. The device that accelerates the separation with the help of centrifugal force is known as ‘Centrifuge’. The centrifuge consists of a fixed base or frame and a rotating part in which the mixture is placed and is then spun at high speed.

13.1 Challenges in the technology transfer process
Technology transfer (TT) is more complex and involves the complex interrelationships between universities, research institutes, the private sector, the state, and society. Though TT is all about translating research findings into purposeful solutions that can support the economy and society, it is not a linear process. The challenges can be described as legal, institutional, cultural, financial, policy, and human resource. All this is accompanied by bottlenecks that inhibit or decelerate the diffusion of promising technologies.
13.1.1 Legal and intellectual property challenges
The vital component of technology transfer is the proper management of intellectual property (IP), which is often the most challenging aspect.
• Ambiguities in IP ownership: During multi-institutional or shared funder research, ownership is quite controversial. As an example, when a government lab and a university collaborate on the project, there is ambiguity as to who would have the ultimate licensing authority over the technology: the university, the lab, or the funding agency. This kind of fight hinders commercialisation and scares off industry partners.
• Lengthy patent filing and prosecution timelines: In several jurisdictions, the filings, examination, and granting of a patent may take between three and five years or more. Such delay is not compatible with the rapid cycle of invention in other fields such as ICT or biotechnology, where patent claims may become invalid before they are granted.
• High costs of IP protection: International direct patenting, like under the Patent Cooperation Treaty (PCT), is costly and involves legal services, fees, and upkeep costs. These costs are excessively high, which cannot be easily compensated by universities and startups, and where technologies are not secured or limited to local markets.

Introduction
The accurate identification of crop varieties is crucial for agriculture, plant breeding, and intellectual property protection. DNA-based techniques have emerged as powerful tools for distinguishing between crop varieties due to their precision and reliability. However, several challenges persist in the adoption and implementation of these techniques. Conventionally, morphological descriptors are routinely used for establishing the identity of varieties. But these morphological descriptors suffer from many drawbacks such as influence of environment on trait expression, epistatic interactions, pleiotrophic effects etc. Furthermore, the paucity of sufficient number of these descriptors for unequivocal identification of increasing number of reference collection of varieties enforces to look for alternatives. Electrophoresis of seed proteins and isozyme analysis have overcome these limitations to some extent but now many powerful DNA based techniques are available. Since all genetic differences between individuals are laid down in the primary sequence of their genomic DNA, the straightforward method of identification of crop varieties and parental lines would be to determine this sequence for the genome under comparison. Sequencing requires huge monitory investment and it is practically impossible to sequence the whole genomes of all varieties. But with the automation in sequencing now possible, short stretches of amplified DNA can be sequenced. However, a more practical strategy would be to limit the comparisons to specific regions of the genome, which frequently differ between individuals.

Raman Spectroscopy

It is a spectroscopic technique based on inelastic scattering of monochromatic light, usually from a laser source. Inelastic scattering means that the frequency of photons in monochromatic light changes upon interaction with a sample. Photons of the laser light are absorbed by the sample and then reemitted. Frequency of the reemitted photons is shifted up or down in comparison with original monochromatic frequency, which is called the Raman effect. This shift provides information about vibrational, rotational and other low frequency transitions in molecules. Raman spectroscopy can be used to study solid, liquid and gaseous samples.

Life is fundamentally a complex interplay of chemical interactions and reactions. Chemistry examines the composition and properties of matter, the interactions between chemical components, and the mechanisms by which complex structures are formed. Biological chemistry, or Biochemistry, delves into these principles within the context of living systems, highlighting the intricate relationships between molecular structure and function. Understanding fundamental chemistry and its application to anatomy and physiology is crucial because the human body is composed entirely of chemical substances. Basic chemistry encompasses the study of matter, its various states, and energy in all its forms. In order to understand the basic chemistry of living let us start from the scratch of learning and remembering everything that we have learnt so far. Matter and Its Properties Anything with mass and occupying space is referred to as matter. Solid, liquid, and gas are its three main states. Mass, distinct from weight, represents the quantity of matter in an object and remains constant regardless of location. In contrast, weight depends on gravitational force. 

Introduction

The metal particles in nanometer scale shows exciting optical and electronic characteristics when compared with respective bulk metals. Because of the inherent electronic properties of the metal and metal oxide nanoparticles these nanostructure materials are applied in various disciplines in recent days. Mostly these nanoparticles can be synthesized either top down or bottom up approaches. The conversion of bigger size particle or matter into tiny particles is called top down approach where as smaller particles or atoms joined together forming particles in regular shape within nanometer scale dimension is called bottom up approach. The formation of nanoparticles by chemical reduction is an example for the later one and the reduction size with the help of mechanical crusing leads to the formation of fine nanoparticles is named as top down approach. Mostly nanoparticles can be synthesized by chemical method because of its easiness to synthesis particles with uniform size and high purity.

Chemical synthesis is spontaneous organization of molecules into stable, structurally well-defined aggregates at the nanometer length scale. Chemical synthesis is largely an art form (i.e., theory often does not quantitatively predict how to make new materials from molecules).Yet, chemical synthesis can be quite powerful (e.g., proteins and complex organic molecules can be made from simple reagents) Semiconductor nanocrystals have been synthesized via “natural self-assembly” in two steps:

1.Capped cluster molecule forms spontaneously from molecular reagents in solution

2.Cluster molecules crystallize out of solution

Synthesis of Zn Oxide Nanoparticle

Aim

To synthesize Zn oxide nanoparticle

Introduction

Zinc oxide nanoparticle are effective anti-bacterial and antiodur agent. They can be synthesized by number of techniques including hydrothermal methods. Their synthesis using solvothermal process is described, (Aneesh et al., 2007).

Chemical Synthesis Methods

Several methods can be used for the production of these nanoparticles, namely: (i) top-down methods (Li et al., 2006) such as vacuum sputtering (Kuhn et al., 2002) or the decomposition of iron penta carbonyl (Fe(CO)5) in organic solvents (Karlsson et al., 2005); and (ii) bottom-up methods that promote the ‘growth’ of the nanostructures via chemical synthesis, for example through the reaction of iron(II) or iron(III) salts with sodium borohydride (Wang and Zhang, 1997). However, these methods present several limitations and problems; the top-down methods are generally expensive and require specific and costly equipment while the drawbacks of the bottom-up approaches are related to safety issues due to the toxicity of sodium borohydride, the production of flammable hydrogen gas during the process (Li et al., 2006), and the tendency to form large agglomerates, very fast and at a high extent, and therefore have a reduced reactivity and degradation efficiency.

The Structure of Proteins

Proteins are composed of building blocks called amino acids. A string of amino acids is called a polypeptide chain. Once such a chain has folded into its working three-dimensional shape, it is a protein. Though there are tens of thousands of different proteins, all of them are put together from a starting set of 20 amino acids. It is the order in which the amino acids are linked in a polypeptide chain that determines which protein will be produced.

Chi-Square

The Chi-square test (c₂) proposed by Karl Pearson in 1899 is used to measure goodness of fit of observed and theoretical or expected data and is a continuous distribution.

Formula for Chi-Square

1. General Formula

The general formula for Chi-square is as follows

Chickpea (Cicer arietinum L.) is a self-pollinating diploid (2n=2x=16) with a genome size of 740 Mbp and belongs to family Fabaceae (or Leguminosae). In a scientific advance involving scientists from more than 20 research organizations, sequencing of the chickpea genome was recently completed for 90 chickpea genotypes, including several wild species. The researchers responsible for the work, led by ICRISAT, succeeded in identifying more than 28,000 genes and several million genetic markers that scientists expect will lead to the development of superior varieties.

China aster is a popular annual cut flower valued for its vibrant colours, sturdy stems, attractive flower forms and good vase life. This chapter describes its origin, distribution, genetics, botanical characteristics and commercial importance in India. It covers improved varieties, climate, soil, propagation, seed treatment, nursery management, planting, nutrition, irrigation and other cultural practices. The chapter further explains pest and disease management, harvesting, postharvest handling, grading, marketing and yield. China aster's importance to small and marginal farmers and its demand as both cut and loose flower make it an attractive crop for diversified commercial floriculture.

China aster (Callistephus chinensis) is a half-hardy annual belonging to the family Asteraceae and is valued for its attractive flowers in various colours and forms. It is an important ornamental and loose flower crop, particularly suitable for garlands and floral decoration. The chapter introduces its origin, genetics, botanical characteristics and important cultivars developed by Indian research institutions. It discusses climate and soil requirements, propagation, nursery management, field preparation, planting and nutrient management. Irrigation and other cultural practices are presented along with major insect pests and diseases such as grey mould and rust. Harvesting, postharvest handling and yield considerations complete the production package

Mutation in M₂

The output of mutations in M₂ and subsequent generations solely depends upon the complex interaction between many factors in the treated organism together with the specific modes of action of particular mutagen. These results are expressed quantitatively by the mutation rate and qualitatively by the mutation spectrum. The proportion of mutated plants to normal ones which is the mutation rate can be computed on the number of mutations per 100 M₁ plants (Gustafsson, 1940), number of mutations per 100 M₁ spikes (Stadler, 1928), and number of mutants per 100 M₂ plants (Gaul, 1960). After comparing the three indices, Gaul (1960) has concluded that mutants per 100 M₂ plants provided the best index, as it is proportional to the initial mutation rate and is independent of variations in progeny size and size of mutated sector. In Pisum, Blixt (1966) has confirmed this. Mohan Rao (1972) has reported that in barley, the M₂ seedling method determined the total induced mutation frequency. This method is also superior since it accounted for the components of induced mutation frequency viz., the frequency of mutated initials in each spike primordium and the frequency of spike primordia mutated.

The qualitative output of mutation in M₂ and later generations is expressed as the mutation spectrum which reflects the different frequencies of different mutations. Westergard (1960) found that the alkylating chemicals induced a higher proportion of less drastic mutations such as Viridis compared to extreme mutations such as Albina than those induced by radiations because of their apparent slight effect on chromosomes. Sidorova (1966) found a positive correlation between the spectrum of chlorophyll and the spectrum of morphological mutations.

Research related to biochemical analysis has been greatly benefited due to the development of chromatographic technique, since this technique makes it possible to resolve mixtures of closely related substances on a milligram to picogram range and to identify individual components by comparison with reference standard compounds. Chromatography ‘gives information where other analytical means have failed’ [Tswett, M. (1906) The macro-chemical and micro-chemical detection of carotene. Ber. Deut. Botan.Ges. 24 : 384- 393].