Variations within populations can be either genetic or non-genetic. Non-genetic variations include individual variations over time (age or seasonal variations), social variations, and ecological variations caused by different habitats or environmental conditions. Genetic variations are inherited and include sexual dimorphism where males and females differ, gynandromorphs which have both male and female characteristics in different parts of the body, and intersexes that have mosaic sex characteristics. Understanding these natural variations is important for taxonomists to accurately identify and classify species.
The process by which a new species develops from the existing species is known as speciation.
Charles Darwin was the first to describe the role of natural selection in speciation in his 1859 book On the Origin of Species. He also identified sexual selection as a likely mechanism, but found it problematic.
A species can be defined as one or more populations of interbreeding organisms that are reproductively isolated in nature from all other organisms.
When populations no longer interbreed, they are thought to be separate species.
There are four geographic modes of speciation in nature, based on the extent to which speciating populations are isolated from one another: allopatric, peripatric, Parapatric, and sympatric.
Speciation may also be induced artificially, through animal husbandry, agriculture, or laboratory experiments.
Allopatric speciation: It is regarded as the most common type of speciation. It involves the physical separation of a species into two groups. This may occur due to climatic changes, movement of tectonic plates leading to the fragmentation of a mass of land, or eruption of a land mass, formation of waterways, or due to the presence of an impassable mountain range.
Parapatric mode of speciation: It occurs due to partial spatial isolation of populations, and is characterized by a small overlap in their ranges as well as significant gene flow amongst the populations. However, the gene flow reduces due to changes in the local conditions, and the two populations become reproductively isolated.
Sympatric mode of speciation: It involves the formation of new species due to a genetic divergence among a few members of the species inhabiting a single geographic area. Unlike the other modes of speciation, here genetic divergence does not arise due to increase in geographic distance, but occurs within the same niche.
Peripatric speciation was Proposed by Ernst Mayr. In this type of speciation, a small group of members inhabiting a peripheral region of the range undergo reproductive isolation to form a new species. Many a time, it is considered to be a variation of allopatric speciation.
The process by which a new species develops from the existing species is known as speciation.
Charles Darwin was the first to describe the role of natural selection in speciation in his 1859 book On the Origin of Species. He also identified sexual selection as a likely mechanism, but found it problematic.
A species can be defined as one or more populations of interbreeding organisms that are reproductively isolated in nature from all other organisms.
When populations no longer interbreed, they are thought to be separate species.
There are four geographic modes of speciation in nature, based on the extent to which speciating populations are isolated from one another: allopatric, peripatric, Parapatric, and sympatric.
Speciation may also be induced artificially, through animal husbandry, agriculture, or laboratory experiments.
Allopatric speciation: It is regarded as the most common type of speciation. It involves the physical separation of a species into two groups. This may occur due to climatic changes, movement of tectonic plates leading to the fragmentation of a mass of land, or eruption of a land mass, formation of waterways, or due to the presence of an impassable mountain range.
Parapatric mode of speciation: It occurs due to partial spatial isolation of populations, and is characterized by a small overlap in their ranges as well as significant gene flow amongst the populations. However, the gene flow reduces due to changes in the local conditions, and the two populations become reproductively isolated.
Sympatric mode of speciation: It involves the formation of new species due to a genetic divergence among a few members of the species inhabiting a single geographic area. Unlike the other modes of speciation, here genetic divergence does not arise due to increase in geographic distance, but occurs within the same niche.
Peripatric speciation was Proposed by Ernst Mayr. In this type of speciation, a small group of members inhabiting a peripheral region of the range undergo reproductive isolation to form a new species. Many a time, it is considered to be a variation of allopatric speciation.
Species are groups of actually or potentially interbreeding populations which are reproductively isolated from other such groups. The biological species concept has been prevalent in the evolutionary literature for the last several decades and is emphasized in many college-level biology courses. It is probably the species concept most familiar to biologists in diverse fields, such as conservation biology, forestry, fisheries, and wildlife management. Species defined by the biological species concept have also been championed as units of conservation. The species concept for most phycologists is based on the morphological characters and hence the term ‘species’ means morphospecies. On the other hand, for evolutionary biologists, the term means biological species that can be defined as a reproductive community of populations (reproductively isolated from others) that occupy a specific niche in Nature.
Speciation is the evolutionary process by which reproductively isolated biological populations evolve to become distinct species.There are few mechanisms through which this process can be well understood.
Organisms are classified into a hierarchical classification that groups closely related individuals.
The species is the basic biological unit around which classifications are based.
KEY POINTS
Evolution is a slow and gradual STEP BY STEP process.
Irreversible transformations takes place from simple to complex or advanced occurring in time and space.
Darwin assumed that if evolution is gradual , then there should be a record in fossils of small incremental change within a species. But in many cases, Darwin, and scientists today, are unable to find most of these intermediate forms.
Mutation, genetic drift, gene flow, non-random mating, and natural selection are the 5 key mechanisms responsible for evolution.
Variation, inheritance, selection and time are the 4 principles that are considered as the components of the evolutionary mechanism of natural selection.
Species are groups of actually or potentially interbreeding populations which are reproductively isolated from other such groups. The biological species concept has been prevalent in the evolutionary literature for the last several decades and is emphasized in many college-level biology courses. It is probably the species concept most familiar to biologists in diverse fields, such as conservation biology, forestry, fisheries, and wildlife management. Species defined by the biological species concept have also been championed as units of conservation. The species concept for most phycologists is based on the morphological characters and hence the term ‘species’ means morphospecies. On the other hand, for evolutionary biologists, the term means biological species that can be defined as a reproductive community of populations (reproductively isolated from others) that occupy a specific niche in Nature.
Speciation is the evolutionary process by which reproductively isolated biological populations evolve to become distinct species.There are few mechanisms through which this process can be well understood.
Organisms are classified into a hierarchical classification that groups closely related individuals.
The species is the basic biological unit around which classifications are based.
KEY POINTS
Evolution is a slow and gradual STEP BY STEP process.
Irreversible transformations takes place from simple to complex or advanced occurring in time and space.
Darwin assumed that if evolution is gradual , then there should be a record in fossils of small incremental change within a species. But in many cases, Darwin, and scientists today, are unable to find most of these intermediate forms.
Mutation, genetic drift, gene flow, non-random mating, and natural selection are the 5 key mechanisms responsible for evolution.
Variation, inheritance, selection and time are the 4 principles that are considered as the components of the evolutionary mechanism of natural selection.
edexcel gcse core science, biology one (B1)jubbi01
detailed notes on each chapter of biology one, core science exam board edexcel.
includes visually engaging elements and useful relevant information.
-science
-core science
-biology
-gcse
-edexcel
Toxic effects of heavy metals : Lead and Arsenicsanjana502982
Heavy metals are naturally occuring metallic chemical elements that have relatively high density, and are toxic at even low concentrations. All toxic metals are termed as heavy metals irrespective of their atomic mass and density, eg. arsenic, lead, mercury, cadmium, thallium, chromium, etc.
THE IMPORTANCE OF MARTIAN ATMOSPHERE SAMPLE RETURN.Sérgio Sacani
The return of a sample of near-surface atmosphere from Mars would facilitate answers to several first-order science questions surrounding the formation and evolution of the planet. One of the important aspects of terrestrial planet formation in general is the role that primary atmospheres played in influencing the chemistry and structure of the planets and their antecedents. Studies of the martian atmosphere can be used to investigate the role of a primary atmosphere in its history. Atmosphere samples would also inform our understanding of the near-surface chemistry of the planet, and ultimately the prospects for life. High-precision isotopic analyses of constituent gases are needed to address these questions, requiring that the analyses are made on returned samples rather than in situ.
Slide 1: Title Slide
Extrachromosomal Inheritance
Slide 2: Introduction to Extrachromosomal Inheritance
Definition: Extrachromosomal inheritance refers to the transmission of genetic material that is not found within the nucleus.
Key Components: Involves genes located in mitochondria, chloroplasts, and plasmids.
Slide 3: Mitochondrial Inheritance
Mitochondria: Organelles responsible for energy production.
Mitochondrial DNA (mtDNA): Circular DNA molecule found in mitochondria.
Inheritance Pattern: Maternally inherited, meaning it is passed from mothers to all their offspring.
Diseases: Examples include Leber’s hereditary optic neuropathy (LHON) and mitochondrial myopathy.
Slide 4: Chloroplast Inheritance
Chloroplasts: Organelles responsible for photosynthesis in plants.
Chloroplast DNA (cpDNA): Circular DNA molecule found in chloroplasts.
Inheritance Pattern: Often maternally inherited in most plants, but can vary in some species.
Examples: Variegation in plants, where leaf color patterns are determined by chloroplast DNA.
Slide 5: Plasmid Inheritance
Plasmids: Small, circular DNA molecules found in bacteria and some eukaryotes.
Features: Can carry antibiotic resistance genes and can be transferred between cells through processes like conjugation.
Significance: Important in biotechnology for gene cloning and genetic engineering.
Slide 6: Mechanisms of Extrachromosomal Inheritance
Non-Mendelian Patterns: Do not follow Mendel’s laws of inheritance.
Cytoplasmic Segregation: During cell division, organelles like mitochondria and chloroplasts are randomly distributed to daughter cells.
Heteroplasmy: Presence of more than one type of organellar genome within a cell, leading to variation in expression.
Slide 7: Examples of Extrachromosomal Inheritance
Four O’clock Plant (Mirabilis jalapa): Shows variegated leaves due to different cpDNA in leaf cells.
Petite Mutants in Yeast: Result from mutations in mitochondrial DNA affecting respiration.
Slide 8: Importance of Extrachromosomal Inheritance
Evolution: Provides insight into the evolution of eukaryotic cells.
Medicine: Understanding mitochondrial inheritance helps in diagnosing and treating mitochondrial diseases.
Agriculture: Chloroplast inheritance can be used in plant breeding and genetic modification.
Slide 9: Recent Research and Advances
Gene Editing: Techniques like CRISPR-Cas9 are being used to edit mitochondrial and chloroplast DNA.
Therapies: Development of mitochondrial replacement therapy (MRT) for preventing mitochondrial diseases.
Slide 10: Conclusion
Summary: Extrachromosomal inheritance involves the transmission of genetic material outside the nucleus and plays a crucial role in genetics, medicine, and biotechnology.
Future Directions: Continued research and technological advancements hold promise for new treatments and applications.
Slide 11: Questions and Discussion
Invite Audience: Open the floor for any questions or further discussion on the topic.
Salas, V. (2024) "John of St. Thomas (Poinsot) on the Science of Sacred Theol...Studia Poinsotiana
I Introduction
II Subalternation and Theology
III Theology and Dogmatic Declarations
IV The Mixed Principles of Theology
V Virtual Revelation: The Unity of Theology
VI Theology as a Natural Science
VII Theology’s Certitude
VIII Conclusion
Notes
Bibliography
All the contents are fully attributable to the author, Doctor Victor Salas. Should you wish to get this text republished, get in touch with the author or the editorial committee of the Studia Poinsotiana. Insofar as possible, we will be happy to broker your contact.
(May 29th, 2024) Advancements in Intravital Microscopy- Insights for Preclini...Scintica Instrumentation
Intravital microscopy (IVM) is a powerful tool utilized to study cellular behavior over time and space in vivo. Much of our understanding of cell biology has been accomplished using various in vitro and ex vivo methods; however, these studies do not necessarily reflect the natural dynamics of biological processes. Unlike traditional cell culture or fixed tissue imaging, IVM allows for the ultra-fast high-resolution imaging of cellular processes over time and space and were studied in its natural environment. Real-time visualization of biological processes in the context of an intact organism helps maintain physiological relevance and provide insights into the progression of disease, response to treatments or developmental processes.
In this webinar we give an overview of advanced applications of the IVM system in preclinical research. IVIM technology is a provider of all-in-one intravital microscopy systems and solutions optimized for in vivo imaging of live animal models at sub-micron resolution. The system’s unique features and user-friendly software enables researchers to probe fast dynamic biological processes such as immune cell tracking, cell-cell interaction as well as vascularization and tumor metastasis with exceptional detail. This webinar will also give an overview of IVM being utilized in drug development, offering a view into the intricate interaction between drugs/nanoparticles and tissues in vivo and allows for the evaluation of therapeutic intervention in a variety of tissues and organs. This interdisciplinary collaboration continues to drive the advancements of novel therapeutic strategies.
Earliest Galaxies in the JADES Origins Field: Luminosity Function and Cosmic ...Sérgio Sacani
We characterize the earliest galaxy population in the JADES Origins Field (JOF), the deepest
imaging field observed with JWST. We make use of the ancillary Hubble optical images (5 filters
spanning 0.4−0.9µm) and novel JWST images with 14 filters spanning 0.8−5µm, including 7 mediumband filters, and reaching total exposure times of up to 46 hours per filter. We combine all our data
at > 2.3µm to construct an ultradeep image, reaching as deep as ≈ 31.4 AB mag in the stack and
30.3-31.0 AB mag (5σ, r = 0.1” circular aperture) in individual filters. We measure photometric
redshifts and use robust selection criteria to identify a sample of eight galaxy candidates at redshifts
z = 11.5 − 15. These objects show compact half-light radii of R1/2 ∼ 50 − 200pc, stellar masses of
M⋆ ∼ 107−108M⊙, and star-formation rates of SFR ∼ 0.1−1 M⊙ yr−1
. Our search finds no candidates
at 15 < z < 20, placing upper limits at these redshifts. We develop a forward modeling approach to
infer the properties of the evolving luminosity function without binning in redshift or luminosity that
marginalizes over the photometric redshift uncertainty of our candidate galaxies and incorporates the
impact of non-detections. We find a z = 12 luminosity function in good agreement with prior results,
and that the luminosity function normalization and UV luminosity density decline by a factor of ∼ 2.5
from z = 12 to z = 14. We discuss the possible implications of our results in the context of theoretical
models for evolution of the dark matter halo mass function.
Deep Behavioral Phenotyping in Systems Neuroscience for Functional Atlasing a...Ana Luísa Pinho
Functional Magnetic Resonance Imaging (fMRI) provides means to characterize brain activations in response to behavior. However, cognitive neuroscience has been limited to group-level effects referring to the performance of specific tasks. To obtain the functional profile of elementary cognitive mechanisms, the combination of brain responses to many tasks is required. Yet, to date, both structural atlases and parcellation-based activations do not fully account for cognitive function and still present several limitations. Further, they do not adapt overall to individual characteristics. In this talk, I will give an account of deep-behavioral phenotyping strategies, namely data-driven methods in large task-fMRI datasets, to optimize functional brain-data collection and improve inference of effects-of-interest related to mental processes. Key to this approach is the employment of fast multi-functional paradigms rich on features that can be well parametrized and, consequently, facilitate the creation of psycho-physiological constructs to be modelled with imaging data. Particular emphasis will be given to music stimuli when studying high-order cognitive mechanisms, due to their ecological nature and quality to enable complex behavior compounded by discrete entities. I will also discuss how deep-behavioral phenotyping and individualized models applied to neuroimaging data can better account for the subject-specific organization of domain-general cognitive systems in the human brain. Finally, the accumulation of functional brain signatures brings the possibility to clarify relationships among tasks and create a univocal link between brain systems and mental functions through: (1) the development of ontologies proposing an organization of cognitive processes; and (2) brain-network taxonomies describing functional specialization. To this end, tools to improve commensurability in cognitive science are necessary, such as public repositories, ontology-based platforms and automated meta-analysis tools. I will thus discuss some brain-atlasing resources currently under development, and their applicability in cognitive as well as clinical neuroscience.
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
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/
2. Variations
Variations within a population is known as intrapopulational variations.
Different individuals belonging the same species may be very different
like some species contains various phena. Often a phenon of one species
resemble a corresponding phenon of another species much more closely
that it does with any other phenon of the same species. This is called
intrapopulational variations or individual variations. For example, the
females of some species birds and insects more closely resemble the
females of other species than the males of its own species. These
individual varaints is a source of confusion for most of taxonomists. Thus
a thorough knowledge of individual variations is essential for taxonomist.
4. Non Genetic Variations
Those variations in an individual that belong to same interbreeding
population and are non-inherited are called non genetic variations or
extrinsic variations. In preserved museum specimen it is impossible to
determine whether a given variant has a genetic basis or not. Nevertheless, it
is important for the taxonomist to understand that many types of variation
exist and it is usually possible to make valid conclusion about the status of a
given variant on the basis of field observation and available experimental
evidence.
5. Types of Non Genetic Variations
Individual Variations in Time: individual variations in time may be either age variations or seasonal
variations.
Age Variations: There are many larval stages in the life of some animals during which they are quietly
different, which cause confusion to taxonomist. In reptiles, birds and mammals there are no larval
stages but still their young ones differ from the adult stages. In fishes the young forms are so different
from the adult that they are often placed in different families. For example, young eel (Anguilla) and
caterpillars are quite different from their adults. The free living larvae of sessile coelenterates, the
larvae of molluscs, echinoderms and insects are quite different from their adults. The cercaria stage
larva of liver fluke does not resemble the adult, similarly in young deer there are less antlers than old
deer, all this cause confusion to taxonomists.
Seasonal Variations in an individual: The animal appearance varies with the seasons during the year. Many birds
like ducks, shore birds, warblers and tangers have bright nuptial plumage during breeding season
which become dull after the breeding season. Aortic fox have grey colour in summer and white
appearance during winter. Similarly polar bear have grey appearance in summer and white in winter.
6. Types of Non Genetic Variations
Individual Variations in Time:
Seasonal Variations in consecutive generations: Many species of short lived invertebrates,
particularly, insects produce several generations in the course of year i.e. the
new forms of spring are quite different from the young ones produced in
summer. Similarly the individuals produced in the wet season differ from those
produced in the dry season. In some tropical butterflies this phenomenon of
dry and wet weather is more prominent.
Cyclomorphosis: It is a special kind of seasonal variation where the population of a
species undergo regular morphological changes throughout the season due to
different kind of food, changes in temperature etc. This phenomenon is present
in fresh water organisms like Daphnia, Rotifers and Cladocerans.
7. Non Genetic Variations
Social Variations: In social insects such as bees, wasps and termites
have different forms of individuals in their colonies (Queen, Worker,
Drone and soldier). These different forms are due to different food or
hormonal control.
Ecological Variations: The different forms of a species produced due to
different environmental conditions. It may be of the following types.
Habitat Variations (Ecophenotypic): Population of a single species that occur in
different habitats in the same region are often visibly different. In snails
and mussels there are different forms in different habitats and often they
are considered as different species.
8. Non Genetic Variations: Ecological
Variations induced by temporary Climatic Conditions: Some animals like fish have
highly unusual phenotypic conditions throughout the year due to
unusual conditions like drought, cold and food supply.
Host-Determined Variations: The same species of a parasite have different forms
in different hosts. As in different hosts, the conditions are different so
the parasite morphology is changed accordingly to adapt to the host
body conditions. Ebeling in 1938 studied variations in the scale insect
“Lecanum corni” grown on different hosts. Those of the apricot were
having large bodies and short appendages as compared to those from
Christmas berry which was having small bodies and long appendages.
9. Non Genetic Variations: Ecological
Density Dependent Variations: The effect of crowding is some time reflected in
morphological variation. Uvarov (1921) has shown that gregarious
species of locusts exist in three unstable biological phases; solitary,
gregarious and transitional. These phases differ in anatomy, colour and
behaviour causing problems for the taxonomists.
Allometric Variations: It is the disproportionate growth of a structure in
relation to the rest of the body. This phenomenon is well known in
insects which involves disproportionate growth of head in ants,
mandibles in stag beetle etc.
10. Non Genetic Variations: Ecological
Neurogenic or Neurohormonal Variations: It refers to colour change in individuals in
response to environment. These changes are accomplished through the
concentration or dispersal of colour bearing bodies called
chromatophores. Such variations were first studied in chameleon. The
same phenomenon of colour change called metachrosis is also found in
crustaceans, cephalopods and cold-blooded vertebrates.
11. Non Genetic Variations
Traumatic (Injury or Disease) Variations: Traumatic variations occur with varying
frequency in different groups of animals. The abnormal nature of this type of
variation is usually obvious, but in some cases it is subtle and may misleading.
There are three types of this variation.
Parasitic induced Variations: Apart from the familiar effects of parasitism as
swelling, distortion and mechanical injury, parasites also produce conspicuous
structural and morphological variations in the host due to parasitism. For example,
when stylop (bee parasite) enters the bee, the head size of the bee is reduced
abdomen enlarges and wing venation changes.
12. Non Genetic Variations
Accidental/Terotological Variations: Accidental variations are usually extremely induced although
it may work internally through some developmental or hormonal system. Such variations are
extremely diverse and in most animals may be readily identified, because such individuals deviate
markedly from the type on those forms which undergo metamorphosis. Injuries to an earlier stage
may produce later abnormalities which are not easily recognized. For example, in beetles certain
types of pupal injury may produce symmetrical abnormalities in punctation, surface sculpturing or
segmentation of the appendages. In butterflies it may result in symmetrical modification of wing
pattern. In most cases even with such clearly notable differences the abnormal nature of the variation
may be detected by a specialist without much difficulty.
Post-mortem changes: In many groups of animals, it is impossible to prevent post-mortem changes
of preserved specimens. For example, orange yellow bird of paradise fade to white in collections. The
Plumage of the chines jay white in life, but turns to blue in collection due to loss of volatile yellow
component in the pigment. Similarly yellow wasp when exposed to cyanide for preservation it gets
bright red.
13. Genetic Variations
The variations in an individual that belong to the same interbreeding populations and
which are inherited are called Genetic, inherited or intrinsic variations. There are
three types of genetic variations.
Musca Spp
14. Genetic Variations: Types
Sexual Dimorphism
The difference between male and female is known as sexual dimorphism. In this case the
male and female are differentiated from one another. These are sex associated variations
which may be
Primary Sex difference: The difference between male and female at the time of birth is
called primary sex difference like gonads and genitalia.
Secondary Sex difference: The difference between male and female which occurs after
puberty is called secondary sex differences. For example, the king parrot, Electus roratus, of
the Paupan region in which the male is green with an orange bill and the female is red with
black bill. Both of these male and female were considered as different species for nearly 100
years which was later on proved by naturalist that they bonged to the same species.
Similarly the males of African ant Dorylus were so unlike than other ant species that they
were not considered as ant for a long time ant was put in different family. Similarly in some
wasps, the females have small wings and males have long and are so different that some
taxonomists used a different nomenclature for the two sexes.
16. Genetic Variations: Types
Gynandromorphs
The individuals that show male characters in
one part of the body and female characters in
other part of the body. Thus the two halves of
the body have different sexes. In these
organisms the sex characters are scattered in
mosaic form. They are produced by unequal
somatic distribution of chromosomes,
particularly sex chromosomes. For example,
Gynandromorphs of alfa alfa butterfly, (Papilis
dardanus) has the left wing of female and the
right wing of male.
17. Genetic Variations: Types
Intersexes: Intersexes are
individuals with mosaic sex.
These are likely to exhibit a
blending of male and female
characters. It is due to either
hormonal imbalance or due
to male and female tendency
genes. Intersexes have been
studied in Lymantria (genus
of moth).
18. Genetic Variations: Types
Reproductively Different
Generations
In many insects one generation
alternates the other generation and
each generation differs from one
another, this is very confusing to
taxonomists. For example, in genus
Cynips (gall wasps) the agamic
generation is so different from the
bisexual one that it has given
different scientific names. Similarly
in the aphids (plant lice) the
parthenogenetic wingless females ae
very different from the winged
females of sexual generation.
20. Genetic Variations: Types
Ordinary Genetic Variation
These variations do not involve sex characters and is of Two types
Discontinuous Variations or Poly Morphism and Continuous Variations
Polymorphism:
The same individual with different shapes (appearance) are polymorphic individuals and the
phenomenon is called polymorphism. In many species of Hemiptera and Coleoptera, the same
population contain flying and flightless individuals. The spotting in lady beetles (Coccinellidae) is well
known example of genetic polymorphism, as industrial melanism in moths. Alfalfa butterfly, Colias
eurytheme, have different female forms, on is white and the other resembling the orange-coloured male.
The African Swallowtail butterflies of the genus Papilio have one male form and five female forms.
Alfa alfa Butterfly Melania Snail
21. Genetic Variations: Types
Ordinary Genetic Variation
Continuous Variations
The commonest type of individual variations is due to slight genetic differences among individuals. No
two individuals (except monozygotic twins) in a population are exactly alike genetically or
morphologically. These differences are very slight and only detected by special techniques. A model
study of variability based on 2877 skins of the house sparrow (Passer domesticus) has been presented by
Selander and Johnston (1967). Among their skin colours each character showed different degree of
variability within a single population. The species of the snail genus Melania (fresh water and brackish
water) have been described largely on the basis of shell characters, so some have spines and spiral ribs
while absent in other members of the genus.
Alfa alfa Butterfly Melania Snail